Dražić, Dragutin M.

Link to this page

Authority KeyName Variants
f40427b6-5061-4d8f-853c-5a243011a4ed
  • Dražić, Dragutin M. (38)
Projects

Author's Bibliography

Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel

Bajat, Jelena; Mišković-Stanković, Vesna; Popić, Jovan; Dražić, Dragutin M.

(Elsevier, 2008)

TY  - JOUR
AU  - Bajat, Jelena
AU  - Mišković-Stanković, Vesna
AU  - Popić, Jovan
AU  - Dražić, Dragutin M.
PY  - 2008
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4117
AB  - The influence of hot-dip galvanized steel (HDG) surface pretreatment with phosphate coatings on the corrosion stability and adhesion characteristics of epoxy coatings electrodeposited on HDG steel was investigated. Phosphate coatings were deposited on hot-dip galvanized steel from baths with different concentrations of NaF (0.1, 0.5 and 1.0 g dm-3) and at different temperatures (50, 65 and 80 °C). The influence of fluoride ion concentration in the phosphating bath, as well as the deposition temperature of the bath, on the adhesion characteristics and corrosion stability of epoxy coatings on phosphated HDG steel was investigated. The dry and wet adhesions were measured by a direct pull-off standardized procedure, as well as indirectly by NMP test, while corrosion stability was investigated by electrochemical impedance spectroscopy (EIS). It was shown that under dry testing conditions all the samples exhibited very good adhesion. However, the different trends of adhesion loss of different protective systems during exposure to corrosive agent (3% NaCl solution) were observed. The lowest adhesion values were obtained for epoxy coating on hot-dip galvanized steel, while the phosphate pretreatments significantly increase the adhesion of epoxy coatings. The highest values of adhesion strength were obtained for epoxy coating on HDG steel modified by phosphate coating deposited at 65 °C with 0.5 g dm-3 NaF in the phosphating bath. EIS measurements in 3% NaCl solution are in accordance with adhesion measurements, i.e. greater values of charge-transfer resistance and smaller values of double-layer capacitance were obtained, as compared to other protective systems.
PB  - Elsevier
T2  - Progress in Organic Coatings
T1  - Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel
VL  - 63
IS  - 2
SP  - 201
EP  - 208
DO  - 10.1016/j.porgcoat.2008.06.002
ER  - 
@article{
author = "Bajat, Jelena and Mišković-Stanković, Vesna and Popić, Jovan and Dražić, Dragutin M.",
year = "2008",
abstract = "The influence of hot-dip galvanized steel (HDG) surface pretreatment with phosphate coatings on the corrosion stability and adhesion characteristics of epoxy coatings electrodeposited on HDG steel was investigated. Phosphate coatings were deposited on hot-dip galvanized steel from baths with different concentrations of NaF (0.1, 0.5 and 1.0 g dm-3) and at different temperatures (50, 65 and 80 °C). The influence of fluoride ion concentration in the phosphating bath, as well as the deposition temperature of the bath, on the adhesion characteristics and corrosion stability of epoxy coatings on phosphated HDG steel was investigated. The dry and wet adhesions were measured by a direct pull-off standardized procedure, as well as indirectly by NMP test, while corrosion stability was investigated by electrochemical impedance spectroscopy (EIS). It was shown that under dry testing conditions all the samples exhibited very good adhesion. However, the different trends of adhesion loss of different protective systems during exposure to corrosive agent (3% NaCl solution) were observed. The lowest adhesion values were obtained for epoxy coating on hot-dip galvanized steel, while the phosphate pretreatments significantly increase the adhesion of epoxy coatings. The highest values of adhesion strength were obtained for epoxy coating on HDG steel modified by phosphate coating deposited at 65 °C with 0.5 g dm-3 NaF in the phosphating bath. EIS measurements in 3% NaCl solution are in accordance with adhesion measurements, i.e. greater values of charge-transfer resistance and smaller values of double-layer capacitance were obtained, as compared to other protective systems.",
publisher = "Elsevier",
journal = "Progress in Organic Coatings",
title = "Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel",
volume = "63",
number = "2",
pages = "201-208",
doi = "10.1016/j.porgcoat.2008.06.002"
}
Bajat, J., Mišković-Stanković, V., Popić, J.,& Dražić, D. M.. (2008). Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel. in Progress in Organic Coatings
Elsevier., 63(2), 201-208.
https://doi.org/10.1016/j.porgcoat.2008.06.002
Bajat J, Mišković-Stanković V, Popić J, Dražić DM. Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel. in Progress in Organic Coatings. 2008;63(2):201-208.
doi:10.1016/j.porgcoat.2008.06.002 .
Bajat, Jelena, Mišković-Stanković, Vesna, Popić, Jovan, Dražić, Dragutin M., "Adhesion characteristics and corrosion stability of epoxy coatings electrodeposited on phosphated hot-dip galvanized steel" in Progress in Organic Coatings, 63, no. 2 (2008):201-208,
https://doi.org/10.1016/j.porgcoat.2008.06.002 . .
64
52
76

Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them

Jegdić, Bore; Dražić, Dragutin M.; Popić, Jovan P.

(2008)

TY  - JOUR
AU  - Jegdić, Bore
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
PY  - 2008
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/473
AB  - Open circuit potential measurements and cyclic voltammetry of chromium and 304 stainless steel in deaerated aqueous H2SO4 solution of pH 1, without and containing NaCl in the concentration range 1-4 M revealed that chromium exhibits two stable open circuit potentials both having the character of a Wagner-Traud corrosion potential. One, Ecorr.1, was established on the passive surface formed by previously exposing Cr to air or by potentiostatic passivation in a controlled manner, and the second one, Ecorr.2, at the bare Cr surface obtained by prolonged cathodic activation. There was a small difference in the Ecorr.1 values depending on the properties of the passive layer. Addition of NaCl accelerates to some extent, the hydrogen evolution reaction on the passive surface, while the same reaction on the bare surface was somewhat inhibited by NaCl. On the other hand, presence of NaCl accelerates the anodic reaction on the bare surface, and it activates the dissolution of the passive layer so that the passivation currents increase with addition of NaCl. This effect is so large that at concentrations of NaCl larger than 3 M, the destruction of the passive layer was so fast that in a matter of seconds the Cr is activated, and the only stable corrosion potential observed was Ecorr.2. No pitting of Cr in the presence of NaCl was observed up to the transpassive potentials. 304 stainless steel could not be activated in sulphuric acid solution, and its open circuit potential, unlike the corrosion potential of the 400 types of stainless steel, was established by the hydrogen evolution reaction on the passive steel surface. The small anodic peak often observed on 304 stainless steel if the metal had been cathodically pre-treated is a pseudo-peak due to the anodic oxidation of hydrogen absorbed inside the metal. This finding should be elaborated more in recommendations (e.g. ASTM standards) for the application of electrochemical corrosion rate measurement to 304 stainless steel corrosion. Addition of NaCl activates the anodic dissolution of steel with the current of the passivation peak being proportional to the NaCl concentration. Unlike chromium, austenitic 304 stainless steel achieves only one corrosion potential in sulphuric acid, both in the presence and absence of NaCl, with the value of ca. -0.200 to -0.350 V (SCE) in the absence and -0.450 V (SCE) in the presence of NaCl, when steel corrodes as the active metal.
T2  - Corrosion Science
T1  - Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them
VL  - 50
IS  - 5
SP  - 1235
EP  - 1244
DO  - 10.1016/j.corsci.2008.01.012
ER  - 
@article{
author = "Jegdić, Bore and Dražić, Dragutin M. and Popić, Jovan P.",
year = "2008",
abstract = "Open circuit potential measurements and cyclic voltammetry of chromium and 304 stainless steel in deaerated aqueous H2SO4 solution of pH 1, without and containing NaCl in the concentration range 1-4 M revealed that chromium exhibits two stable open circuit potentials both having the character of a Wagner-Traud corrosion potential. One, Ecorr.1, was established on the passive surface formed by previously exposing Cr to air or by potentiostatic passivation in a controlled manner, and the second one, Ecorr.2, at the bare Cr surface obtained by prolonged cathodic activation. There was a small difference in the Ecorr.1 values depending on the properties of the passive layer. Addition of NaCl accelerates to some extent, the hydrogen evolution reaction on the passive surface, while the same reaction on the bare surface was somewhat inhibited by NaCl. On the other hand, presence of NaCl accelerates the anodic reaction on the bare surface, and it activates the dissolution of the passive layer so that the passivation currents increase with addition of NaCl. This effect is so large that at concentrations of NaCl larger than 3 M, the destruction of the passive layer was so fast that in a matter of seconds the Cr is activated, and the only stable corrosion potential observed was Ecorr.2. No pitting of Cr in the presence of NaCl was observed up to the transpassive potentials. 304 stainless steel could not be activated in sulphuric acid solution, and its open circuit potential, unlike the corrosion potential of the 400 types of stainless steel, was established by the hydrogen evolution reaction on the passive steel surface. The small anodic peak often observed on 304 stainless steel if the metal had been cathodically pre-treated is a pseudo-peak due to the anodic oxidation of hydrogen absorbed inside the metal. This finding should be elaborated more in recommendations (e.g. ASTM standards) for the application of electrochemical corrosion rate measurement to 304 stainless steel corrosion. Addition of NaCl activates the anodic dissolution of steel with the current of the passivation peak being proportional to the NaCl concentration. Unlike chromium, austenitic 304 stainless steel achieves only one corrosion potential in sulphuric acid, both in the presence and absence of NaCl, with the value of ca. -0.200 to -0.350 V (SCE) in the absence and -0.450 V (SCE) in the presence of NaCl, when steel corrodes as the active metal.",
journal = "Corrosion Science",
title = "Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them",
volume = "50",
number = "5",
pages = "1235-1244",
doi = "10.1016/j.corsci.2008.01.012"
}
Jegdić, B., Dražić, D. M.,& Popić, J. P.. (2008). Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them. in Corrosion Science, 50(5), 1235-1244.
https://doi.org/10.1016/j.corsci.2008.01.012
Jegdić B, Dražić DM, Popić JP. Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them. in Corrosion Science. 2008;50(5):1235-1244.
doi:10.1016/j.corsci.2008.01.012 .
Jegdić, Bore, Dražić, Dragutin M., Popić, Jovan P., "Open circuit potentials of metallic chromium and austenitic 304 stainless steel in aqueous sulphuric acid solution and the influence of chloride ions on them" in Corrosion Science, 50, no. 5 (2008):1235-1244,
https://doi.org/10.1016/j.corsci.2008.01.012 . .
54
45
59

Adhesion of epoxy cataphoretic coatings on Zn alloys

Bajat, Jelena; Mišković-Stanković, Vesna; Dražić, Dragutin M.

(Belgrade : Serbian Chemical Society, 2007)

TY  - JOUR
AU  - Bajat, Jelena
AU  - Mišković-Stanković, Vesna
AU  - Dražić, Dragutin M.
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4303
AB  - One of the most important factors in corrosion prevention by protective coatings is the loss of coating adhesion under environmental influence. In this work, the adhesion of epoxy cataphoretic coatings was examined on steel and steel modified by Zn-Fe and Zn-Co alloys. The dry and wet adhesions of epoxy primers were measured by the direct pull-off standardized procedure, as well as indirectly by the NMP test. The corrosion stability of the coated samples was investigated by electrochemical impedance spectroscopy. It was shown that under dry testing conditions all the samples exhibited very good adhesion. However, different trends of adhesion loss of different protective systems during exposure to a corrosive agent (3 % NaCl solution) were observed. The lowest adhesion values were obtained for epoxy coating on the steel substrate. The change in adhesion of the epoxy coating on steel modified by Zn-Co alloy during immersion in 3 % NaCl solution for 24 days was the smallest of all the investigated samples. Electrochemical impedance measurements in 3 % NaCl solution confirmed the good protective properties of this protective system, i.e., greater values of pore resistance were obtained.
AB  - Један од најважнијих фактора у заштити од корозије органским превлакама је губитак
адхезије органских превлака под утицајем корозионе средине. У овом раду проучавана је ад-
хезија епоксидних катафоретских превлака на челику и челику модификованом легурама
Zn–Fe и Zn–Co. Испитиване су тзв. сува и мокра адхезија стандардним pull-off поступком,
као и NMP тестом. Корозиона стабилност свих узорака је испитивана спектроскопијом елек-
трохемијске импеданције. Сви узорци су имали добру почетну адхезију, међутим током де-
ловања корозионог агенса (3 % NaCl) промена адхезије се значајно разликовала код различи-
тих заштитних система. Најмање вредности адхезије су добијене у случају епоксидне пре-
влаке на челику. Укупно смањење адхезије током 24 дана испитивања је најмање за епок-
сидну превлаку на челику модификованом Zn–Co легуром. Највеће вредности отпорности у
порама епоксидне превлаке током целокупног испитиваног периода деловања корозионог аг-
енса код превлаке на челику модификованом Zn–Co легуром такође указују на велику ста-
билност овог заштитног система.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Adhesion of epoxy cataphoretic coatings on Zn alloys
T1  - Адхезија епоксидних катафоретских превлака на легурама цинка
VL  - 72
VL  - 1392
IS  - 12
SP  - 1383
DO  - 10.2298/JSC0712383B
ER  - 
@article{
author = "Bajat, Jelena and Mišković-Stanković, Vesna and Dražić, Dragutin M.",
year = "2007",
abstract = "One of the most important factors in corrosion prevention by protective coatings is the loss of coating adhesion under environmental influence. In this work, the adhesion of epoxy cataphoretic coatings was examined on steel and steel modified by Zn-Fe and Zn-Co alloys. The dry and wet adhesions of epoxy primers were measured by the direct pull-off standardized procedure, as well as indirectly by the NMP test. The corrosion stability of the coated samples was investigated by electrochemical impedance spectroscopy. It was shown that under dry testing conditions all the samples exhibited very good adhesion. However, different trends of adhesion loss of different protective systems during exposure to a corrosive agent (3 % NaCl solution) were observed. The lowest adhesion values were obtained for epoxy coating on the steel substrate. The change in adhesion of the epoxy coating on steel modified by Zn-Co alloy during immersion in 3 % NaCl solution for 24 days was the smallest of all the investigated samples. Electrochemical impedance measurements in 3 % NaCl solution confirmed the good protective properties of this protective system, i.e., greater values of pore resistance were obtained., Један од најважнијих фактора у заштити од корозије органским превлакама је губитак
адхезије органских превлака под утицајем корозионе средине. У овом раду проучавана је ад-
хезија епоксидних катафоретских превлака на челику и челику модификованом легурама
Zn–Fe и Zn–Co. Испитиване су тзв. сува и мокра адхезија стандардним pull-off поступком,
као и NMP тестом. Корозиона стабилност свих узорака је испитивана спектроскопијом елек-
трохемијске импеданције. Сви узорци су имали добру почетну адхезију, међутим током де-
ловања корозионог агенса (3 % NaCl) промена адхезије се значајно разликовала код различи-
тих заштитних система. Најмање вредности адхезије су добијене у случају епоксидне пре-
влаке на челику. Укупно смањење адхезије током 24 дана испитивања је најмање за епок-
сидну превлаку на челику модификованом Zn–Co легуром. Највеће вредности отпорности у
порама епоксидне превлаке током целокупног испитиваног периода деловања корозионог аг-
енса код превлаке на челику модификованом Zn–Co легуром такође указују на велику ста-
билност овог заштитног система.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Adhesion of epoxy cataphoretic coatings on Zn alloys, Адхезија епоксидних катафоретских превлака на легурама цинка",
volume = "72, 1392",
number = "12",
pages = "1383",
doi = "10.2298/JSC0712383B"
}
Bajat, J., Mišković-Stanković, V.,& Dražić, D. M.. (2007). Adhesion of epoxy cataphoretic coatings on Zn alloys. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 72(12), 1383.
https://doi.org/10.2298/JSC0712383B
Bajat J, Mišković-Stanković V, Dražić DM. Adhesion of epoxy cataphoretic coatings on Zn alloys. in Journal of the Serbian Chemical Society. 2007;72(12):1383.
doi:10.2298/JSC0712383B .
Bajat, Jelena, Mišković-Stanković, Vesna, Dražić, Dragutin M., "Adhesion of epoxy cataphoretic coatings on Zn alloys" in Journal of the Serbian Chemical Society, 72, no. 12 (2007):1383,
https://doi.org/10.2298/JSC0712383B . .
5
5
6

The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel

Bajat, Jelena; Mišković-Stanković, Vesna; Bibić, Nataša M.; Dražić, Dragutin M.

(Elsevier, 2007)

TY  - JOUR
AU  - Bajat, Jelena
AU  - Mišković-Stanković, Vesna
AU  - Bibić, Nataša M.
AU  - Dražić, Dragutin M.
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4331
AB  - The adhesion and electrochemical properties of epoxy coatings electrodeposited on hot-dip galvanized steel with and without passive films were investigated during exposure to 3% NaCl. The passive films were formed in hot air, in boiling water and by chromating. Adhesion was measured both by a standardized pull-off method and by swelling in N-methyl pyrrolidone. Pretreatment of hot-dip galvanized steel with passive film formed in hot air increases both dry and wet adhesion strength of the epoxy coating compared to pretreatment with passive film formed in boiling water and chromate coating. The overall increase of wet adhesion for this sample was maintained throughout the whole investigated time period. It was shown that the change in adhesion of epoxy coating on a chromate coating is smallest of all investigated samples, although the initial value of adhesion on this surface had the lowest value. The corrosion stability of coated Zn samples pretreated by different methods, was investigated by electrochemical impedance spectroscopy and in the initial time of exposure to NaCl the highest values of pore resistance were also obtained for the epoxy coating on Zn pretreated in hot air, whereas the epoxy coating on a HDG steel with a chromate coating showed the smallest change in electrochemical properties (pore resistance, coating capacitance, charge-transfer resistance) during prolonged exposure time.
PB  - Elsevier
T2  - Progress in Organic Coatings
T1  - The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel
VL  - 58
IS  - 4
SP  - 323
EP  - 330
DO  - 10.1016/j.porgcoat.2007.01.011
ER  - 
@article{
author = "Bajat, Jelena and Mišković-Stanković, Vesna and Bibić, Nataša M. and Dražić, Dragutin M.",
year = "2007",
abstract = "The adhesion and electrochemical properties of epoxy coatings electrodeposited on hot-dip galvanized steel with and without passive films were investigated during exposure to 3% NaCl. The passive films were formed in hot air, in boiling water and by chromating. Adhesion was measured both by a standardized pull-off method and by swelling in N-methyl pyrrolidone. Pretreatment of hot-dip galvanized steel with passive film formed in hot air increases both dry and wet adhesion strength of the epoxy coating compared to pretreatment with passive film formed in boiling water and chromate coating. The overall increase of wet adhesion for this sample was maintained throughout the whole investigated time period. It was shown that the change in adhesion of epoxy coating on a chromate coating is smallest of all investigated samples, although the initial value of adhesion on this surface had the lowest value. The corrosion stability of coated Zn samples pretreated by different methods, was investigated by electrochemical impedance spectroscopy and in the initial time of exposure to NaCl the highest values of pore resistance were also obtained for the epoxy coating on Zn pretreated in hot air, whereas the epoxy coating on a HDG steel with a chromate coating showed the smallest change in electrochemical properties (pore resistance, coating capacitance, charge-transfer resistance) during prolonged exposure time.",
publisher = "Elsevier",
journal = "Progress in Organic Coatings",
title = "The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel",
volume = "58",
number = "4",
pages = "323-330",
doi = "10.1016/j.porgcoat.2007.01.011"
}
Bajat, J., Mišković-Stanković, V., Bibić, N. M.,& Dražić, D. M.. (2007). The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel. in Progress in Organic Coatings
Elsevier., 58(4), 323-330.
https://doi.org/10.1016/j.porgcoat.2007.01.011
Bajat J, Mišković-Stanković V, Bibić NM, Dražić DM. The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel. in Progress in Organic Coatings. 2007;58(4):323-330.
doi:10.1016/j.porgcoat.2007.01.011 .
Bajat, Jelena, Mišković-Stanković, Vesna, Bibić, Nataša M., Dražić, Dragutin M., "The influence of zinc surface pretreatment on the adhesion of epoxy coating electrodeposited on hot-dip galvanized steel" in Progress in Organic Coatings, 58, no. 4 (2007):323-330,
https://doi.org/10.1016/j.porgcoat.2007.01.011 . .
49
33
45

Structural effects of metallic chromium on its electrochemical behavior

Jegdić, Bore; Dražić, Dragutin M.; Popić, Jovan P.; Radmilović, Velimir R.

(Serbian Chemical Society, 2007)

TY  - JOUR
AU  - Jegdić, Bore
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
AU  - Radmilović, Velimir R.
PY  - 2007
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/311
AB  - Chromium dissolution in aqueous sulfuric acid solution of pH 1 was studied electrochemically on chromium electrodes with different crystallographic structures. A slow potentiodynamic method was used for the electrochemical measurements in deaerated solutions (purged with nitrogen),while the Cr(III) ions in the solution after the corrosion were determined by atomic absorption spectrometry. Three electrode materials with a very dominant crystallite orientation resembling single crystal structures (i.e., 111 and 110) confirmed by the electron backscattering diffraction (EBSD), were used in the experiments. The (111) structures were somewhat more active electrochemically (both anodic and cathodic) than the (110) structure. However, Cr electrochemically deposited in standard plating bath, assumed from literature data to has also the (111) structure, was more than 4 times active for anodic dissolution and, by the same number, less active for cathodic hydrogen evolution. The concentrations of Cr(III) ions determined in the solution after definite times of corrosion of all the materials showed almost two times larger dissolution rates than observed electrochemically by three different electrochemical methods (Wagner-Traud, Stern-Geary, electrochemical impedance spectroscopy). This is explained by the simultaneous occurrence of potential independent chemical dissolution of Cr, by a direct reaction of metallic Cr with H2O molecules, proposed a long time ago by Kolotyrkin and coworkers. .
AB  - Proučavano je elektrohemijsko rastvaranje hroma u vodenim rastvorima sumporne kiseline (pH 1) sa elektrodama od hroma različite kristalografske strukture. Primenjena je spora potenciodinamička metoda u deaeriranim rastvorima (uz provođenje azota) na 25°C, a joni Cr(III) u rastvoru posle određenog vremena korozije određivani su atomskom apsorpcionom spektroskopijom. U eksperimentima su upotrebljena tri elektrodna materijala sa dominantnim kristalnim strukturama koje podsećaju na mono kristalne (tj. 111 i 110), a što je potvrđeno EBSD metodom. Nađeno je da je struktura (111) elektrohemijski aktivnija (i anodno i katodno) od strukture (110). Međutim, elektrolitički istaložen Cr iz standardnog kupatila za hromiranje, a koji na osnovu literaturnih podataka ima strukturu (111) bio je oko 4 puta aktivniji u anodnoj reakciji i isto toliko manje aktivan za katodnu reakciju izdvajanja vodonika. Analitički određivane koncentracije Cr(III) jona u rastvoru posle određenog vremena spontane korozije pokazivale su dva puta veće koncentracije nego što bi se očekivalo na osnovu brzine elektrohemijske korozije, određivanih metodama Wagner-Traud, Stern-Geary i elektrohemijskom impedansnom spektroskopijom. Ovo je objašnjeno jednovremenim odigravanjem i elektrohemijske reakcije i hemijske reakcije direktnog reagovanja metalnog Cr sa molekulima vode, po mehanizmu predloženom od Kolotirkina i saradnika. .
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Structural effects of metallic chromium on its electrochemical behavior
T1  - Uticaj strukture metalnog hroma na njegovo elektrohemijsko ponašanje
VL  - 72
IS  - 6
SP  - 563
EP  - 578
DO  - 10.2298/JSC0706563J
ER  - 
@article{
author = "Jegdić, Bore and Dražić, Dragutin M. and Popić, Jovan P. and Radmilović, Velimir R.",
year = "2007",
abstract = "Chromium dissolution in aqueous sulfuric acid solution of pH 1 was studied electrochemically on chromium electrodes with different crystallographic structures. A slow potentiodynamic method was used for the electrochemical measurements in deaerated solutions (purged with nitrogen),while the Cr(III) ions in the solution after the corrosion were determined by atomic absorption spectrometry. Three electrode materials with a very dominant crystallite orientation resembling single crystal structures (i.e., 111 and 110) confirmed by the electron backscattering diffraction (EBSD), were used in the experiments. The (111) structures were somewhat more active electrochemically (both anodic and cathodic) than the (110) structure. However, Cr electrochemically deposited in standard plating bath, assumed from literature data to has also the (111) structure, was more than 4 times active for anodic dissolution and, by the same number, less active for cathodic hydrogen evolution. The concentrations of Cr(III) ions determined in the solution after definite times of corrosion of all the materials showed almost two times larger dissolution rates than observed electrochemically by three different electrochemical methods (Wagner-Traud, Stern-Geary, electrochemical impedance spectroscopy). This is explained by the simultaneous occurrence of potential independent chemical dissolution of Cr, by a direct reaction of metallic Cr with H2O molecules, proposed a long time ago by Kolotyrkin and coworkers. ., Proučavano je elektrohemijsko rastvaranje hroma u vodenim rastvorima sumporne kiseline (pH 1) sa elektrodama od hroma različite kristalografske strukture. Primenjena je spora potenciodinamička metoda u deaeriranim rastvorima (uz provođenje azota) na 25°C, a joni Cr(III) u rastvoru posle određenog vremena korozije određivani su atomskom apsorpcionom spektroskopijom. U eksperimentima su upotrebljena tri elektrodna materijala sa dominantnim kristalnim strukturama koje podsećaju na mono kristalne (tj. 111 i 110), a što je potvrđeno EBSD metodom. Nađeno je da je struktura (111) elektrohemijski aktivnija (i anodno i katodno) od strukture (110). Međutim, elektrolitički istaložen Cr iz standardnog kupatila za hromiranje, a koji na osnovu literaturnih podataka ima strukturu (111) bio je oko 4 puta aktivniji u anodnoj reakciji i isto toliko manje aktivan za katodnu reakciju izdvajanja vodonika. Analitički određivane koncentracije Cr(III) jona u rastvoru posle određenog vremena spontane korozije pokazivale su dva puta veće koncentracije nego što bi se očekivalo na osnovu brzine elektrohemijske korozije, određivanih metodama Wagner-Traud, Stern-Geary i elektrohemijskom impedansnom spektroskopijom. Ovo je objašnjeno jednovremenim odigravanjem i elektrohemijske reakcije i hemijske reakcije direktnog reagovanja metalnog Cr sa molekulima vode, po mehanizmu predloženom od Kolotirkina i saradnika. .",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Structural effects of metallic chromium on its electrochemical behavior, Uticaj strukture metalnog hroma na njegovo elektrohemijsko ponašanje",
volume = "72",
number = "6",
pages = "563-578",
doi = "10.2298/JSC0706563J"
}
Jegdić, B., Dražić, D. M., Popić, J. P.,& Radmilović, V. R.. (2007). Structural effects of metallic chromium on its electrochemical behavior. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 72(6), 563-578.
https://doi.org/10.2298/JSC0706563J
Jegdić B, Dražić DM, Popić JP, Radmilović VR. Structural effects of metallic chromium on its electrochemical behavior. in Journal of the Serbian Chemical Society. 2007;72(6):563-578.
doi:10.2298/JSC0706563J .
Jegdić, Bore, Dražić, Dragutin M., Popić, Jovan P., Radmilović, Velimir R., "Structural effects of metallic chromium on its electrochemical behavior" in Journal of the Serbian Chemical Society, 72, no. 6 (2007):563-578,
https://doi.org/10.2298/JSC0706563J . .

Corrosion potential of 304 stainless steel in sulfuric acid

Jegdić, Bore; Dražić, Dragutin M.; Popić, Jovan P.

(Serbian Chemical Society, 2006)

TY  - JOUR
AU  - Jegdić, Bore
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
PY  - 2006
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/257
AB  - The potentiodynamic study of the electrochemical behavior of austenitic 304 stainless steel in deaerated aqueous sulfuric acid of pH 1 revealed that the steel achieved a stable corrosion potential of ca. - 0.350 V (SCE) independent of whether the electrode had previously been cathodically "activated" or anodically passivated. It was also shown that the experimentally observed anodic peak was not the usually obtained anodic passivation peak, as is the case with a number of metal, but an artifact due to the anodic oxidation of hydrogen absorbed during the previously employed cathodic polarization and hydrogen evolution, intended to activate the initially passive surface, or even hydrogen absorbed on the open circuit potential. It was shown that this potential establishes and electrochemical corrosion potential of the Wagner-Traud type due to the evolution of cathodic hydrogen on a passivated steel surface and anodic metal dissolution through the passive layer. It was impossible to activate 304 stainless steel in sulfuric acid of pH 1 by cathodic polarization, and the usually observed anodic peak obtained under these conditions should not be considered as an active metal dissolution process and a passivation anodic peak, but rather as an artifact due to the electrochemical oxidation of the in the steel absorbed hydrogen.
AB  - Potenciodinamička ispitivanja elektrohemijskog ponašanja nerđajućeg čelika 304 u deaeriranoj sumpornoj kiselini sa pH 1 pokazala su da se na čeliku uspostavlja stabilan korozioni potencijal od - 0,350 V(ZKE) nezavisno od toga da li je elektroda prethodno katodno tretirana radi "aktivacije", ili je površina bila pasivirana. Pokazano je, takođe, da eksperimentalno dobijeni anodni maksimum na potenciodinamičkoj krivi pozitivnije od korozionog potencijala nije anodni pasivacioni maksimum koji se obično dobija pri anodnoj polarizaciji većeg broja metala u sličnim uslovima, već eksperimentalni artefakt koji nastaje zbog anodne oksidacije vodonika apsorbovanog unutar čelika tokom katodnog "aktiviranja" ili čak i pri dužem držanju na korozionom potencijalu. Pokazano je da je spontano formirani potencijal otvorenog kola zapravo korozioni potencijal koji nastaje kao mešoviti potencijal Vagner-Traudovog tipa suprotnim delovawem katodne reakcije izdvajanja vodonika na pasivnom sloju i anodnog rastvaranja čelika kroz pasivni sloj. Nije bilo mogućno katodnom "aktivacijom" i dugotrajnijom katodnom polarizacijom do značajno negativnih potencijala i vrlo velikih katodnih struja da se pasivni sloj ukloni i postigne aktivno elektrohemijsko rastvaranje metala bez prisustva pasivnog sloja, tj. slobodna metalna površina. Stoga, često eksperimentalno konstatovan anodni maksimum na ovakvim čelicima ne treba da se interpretira kao anodno rastvaranje sa pasivacionim maksimumom, već kao posledica anodne oksidacije apsorbovanog vodonika u pasivnom čeliku, a koji se pod ovim uslovima ne može elektrohemijski aktivirati, odn. depasivirati.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Corrosion potential of 304 stainless steel in sulfuric acid
T1  - Korozioni potencijal nerđajućeg čelika 304 u sumpornoj kiselini
VL  - 71
IS  - 5
SP  - 543
EP  - 551
DO  - 10.2298/JSC0605543J
ER  - 
@article{
author = "Jegdić, Bore and Dražić, Dragutin M. and Popić, Jovan P.",
year = "2006",
abstract = "The potentiodynamic study of the electrochemical behavior of austenitic 304 stainless steel in deaerated aqueous sulfuric acid of pH 1 revealed that the steel achieved a stable corrosion potential of ca. - 0.350 V (SCE) independent of whether the electrode had previously been cathodically "activated" or anodically passivated. It was also shown that the experimentally observed anodic peak was not the usually obtained anodic passivation peak, as is the case with a number of metal, but an artifact due to the anodic oxidation of hydrogen absorbed during the previously employed cathodic polarization and hydrogen evolution, intended to activate the initially passive surface, or even hydrogen absorbed on the open circuit potential. It was shown that this potential establishes and electrochemical corrosion potential of the Wagner-Traud type due to the evolution of cathodic hydrogen on a passivated steel surface and anodic metal dissolution through the passive layer. It was impossible to activate 304 stainless steel in sulfuric acid of pH 1 by cathodic polarization, and the usually observed anodic peak obtained under these conditions should not be considered as an active metal dissolution process and a passivation anodic peak, but rather as an artifact due to the electrochemical oxidation of the in the steel absorbed hydrogen., Potenciodinamička ispitivanja elektrohemijskog ponašanja nerđajućeg čelika 304 u deaeriranoj sumpornoj kiselini sa pH 1 pokazala su da se na čeliku uspostavlja stabilan korozioni potencijal od - 0,350 V(ZKE) nezavisno od toga da li je elektroda prethodno katodno tretirana radi "aktivacije", ili je površina bila pasivirana. Pokazano je, takođe, da eksperimentalno dobijeni anodni maksimum na potenciodinamičkoj krivi pozitivnije od korozionog potencijala nije anodni pasivacioni maksimum koji se obično dobija pri anodnoj polarizaciji većeg broja metala u sličnim uslovima, već eksperimentalni artefakt koji nastaje zbog anodne oksidacije vodonika apsorbovanog unutar čelika tokom katodnog "aktiviranja" ili čak i pri dužem držanju na korozionom potencijalu. Pokazano je da je spontano formirani potencijal otvorenog kola zapravo korozioni potencijal koji nastaje kao mešoviti potencijal Vagner-Traudovog tipa suprotnim delovawem katodne reakcije izdvajanja vodonika na pasivnom sloju i anodnog rastvaranja čelika kroz pasivni sloj. Nije bilo mogućno katodnom "aktivacijom" i dugotrajnijom katodnom polarizacijom do značajno negativnih potencijala i vrlo velikih katodnih struja da se pasivni sloj ukloni i postigne aktivno elektrohemijsko rastvaranje metala bez prisustva pasivnog sloja, tj. slobodna metalna površina. Stoga, često eksperimentalno konstatovan anodni maksimum na ovakvim čelicima ne treba da se interpretira kao anodno rastvaranje sa pasivacionim maksimumom, već kao posledica anodne oksidacije apsorbovanog vodonika u pasivnom čeliku, a koji se pod ovim uslovima ne može elektrohemijski aktivirati, odn. depasivirati.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Corrosion potential of 304 stainless steel in sulfuric acid, Korozioni potencijal nerđajućeg čelika 304 u sumpornoj kiselini",
volume = "71",
number = "5",
pages = "543-551",
doi = "10.2298/JSC0605543J"
}
Jegdić, B., Dražić, D. M.,& Popić, J. P.. (2006). Corrosion potential of 304 stainless steel in sulfuric acid. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 71(5), 543-551.
https://doi.org/10.2298/JSC0605543J
Jegdić B, Dražić DM, Popić JP. Corrosion potential of 304 stainless steel in sulfuric acid. in Journal of the Serbian Chemical Society. 2006;71(5):543-551.
doi:10.2298/JSC0605543J .
Jegdić, Bore, Dražić, Dragutin M., Popić, Jovan P., "Corrosion potential of 304 stainless steel in sulfuric acid" in Journal of the Serbian Chemical Society, 71, no. 5 (2006):543-551,
https://doi.org/10.2298/JSC0605543J . .
3
19
17
19

Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions

Jegdić, Bore; Dražić, Dragutin M.; Popić, Jovan P.

(Serbian Chemical Society, 2006)

TY  - JOUR
AU  - Jegdić, Bore
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
PY  - 2006
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/274
AB  - Open circuit potential measurements and cyclic voltammetry of chromium in deaerated aqueous H2SO4 solution of pH 1 without and containing NaCl in the concentration range 0.5 - 4 M revealed that chromium exhibits two stable open circuit potentials having the character of a Wagner-Traud corrosion potential. One, E corr.1, was established on the passive surface formed by exposing Cr previously to air or passivated potentiostacially in a controlled manner, and the second one, E corr,2, at the bare Cr surface obtained by prolonged cathodic activation. There is a small difference in the E corr,1 values as a function of the passive layer properties. Addition of NaCl accelerates the hydrogen evolution reaction on the passive surface to some extent, while the same reaction on the bare surface was not affected by NaCl. On the other hand, presence of NaCl accelerates the anodic reaction on the bare surface, and it activates the dissolution of the passive layer so that the passive currents increase with addition of NaCl. This effect is so large that at concentration of NaCl larger than 3 M, the destruction of the passive layer was so fast that in a matter of seconds the Cr was activated, and the only one stable corrosion potential observed was E corr.2. No pitting of Cr in the presence of NaCl was observed up to the transpassive potentials.
AB  - Merenja potencijala otvorenog kola, kao i merenja primenom ciklične voltametrije u deaerisanim vodenim rastvorima H 2SO4, pH1, bez i sa dodatkom NaCl u koncentracionom opsegu 0,5-4M, otkrila su da hrom pokazuje dva stabilna potencijala otvorenog kola koji imaju osobine Wagner-Traud-ovog korozionog potencijala. Jedan korozioni potencijal, E corr.1 , se uspostavljao na pasiviranoj površini, koja se formira prethodnim izlaganjem Cr vazduhu, ili poteciostatskim pasiviranjem na kontrolisan način, a drugi, E corr.2 , se obrazovao na goloj površini Cr koja je formirana katodnom aktivacijom u dovoljno dugom periodu vremena. Postoji izvesna mala razlika u vrednostima E corr.1 kao funkcija osobina pasivnog sloja. Dodatak NaCl u određenoj meri ubrzava reakciju izdvajanja vodonika na pasiviranoj površini, dok NaCl nema uticaja na istu reakciju na goloj površini Cr. Sa druge strane prisustvo NaCl ubrzava anodnu reakciju na goloj površini hroma i aktivira rastvaranje pasivnog sloja, tako da se struja pasivacije povećava sa dodatkom NaCl. Uticaj NaCl je toliko veliki, da pri koncentracijama većim od 3M, razaranje pasivnog sloja postaje brzo, da se Cr za vreme od nekoliko sekundi aktivira i tada se uočava samo jedan stabilni korozioni potencijal E corr.2 . Nije uočena pojava pitinga u prisustvu NaCl, sve do potencijala u transpasivnoj oblasti.
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions
T1  - Uticaj hloridnih jona na potencijal otvorenog kola hroma u deaerisanim rastvorima sumporne kiseline
VL  - 71
IS  - 11
SP  - 1187
EP  - 1194
DO  - 10.2298/JSC0611187J
ER  - 
@article{
author = "Jegdić, Bore and Dražić, Dragutin M. and Popić, Jovan P.",
year = "2006",
abstract = "Open circuit potential measurements and cyclic voltammetry of chromium in deaerated aqueous H2SO4 solution of pH 1 without and containing NaCl in the concentration range 0.5 - 4 M revealed that chromium exhibits two stable open circuit potentials having the character of a Wagner-Traud corrosion potential. One, E corr.1, was established on the passive surface formed by exposing Cr previously to air or passivated potentiostacially in a controlled manner, and the second one, E corr,2, at the bare Cr surface obtained by prolonged cathodic activation. There is a small difference in the E corr,1 values as a function of the passive layer properties. Addition of NaCl accelerates the hydrogen evolution reaction on the passive surface to some extent, while the same reaction on the bare surface was not affected by NaCl. On the other hand, presence of NaCl accelerates the anodic reaction on the bare surface, and it activates the dissolution of the passive layer so that the passive currents increase with addition of NaCl. This effect is so large that at concentration of NaCl larger than 3 M, the destruction of the passive layer was so fast that in a matter of seconds the Cr was activated, and the only one stable corrosion potential observed was E corr.2. No pitting of Cr in the presence of NaCl was observed up to the transpassive potentials., Merenja potencijala otvorenog kola, kao i merenja primenom ciklične voltametrije u deaerisanim vodenim rastvorima H 2SO4, pH1, bez i sa dodatkom NaCl u koncentracionom opsegu 0,5-4M, otkrila su da hrom pokazuje dva stabilna potencijala otvorenog kola koji imaju osobine Wagner-Traud-ovog korozionog potencijala. Jedan korozioni potencijal, E corr.1 , se uspostavljao na pasiviranoj površini, koja se formira prethodnim izlaganjem Cr vazduhu, ili poteciostatskim pasiviranjem na kontrolisan način, a drugi, E corr.2 , se obrazovao na goloj površini Cr koja je formirana katodnom aktivacijom u dovoljno dugom periodu vremena. Postoji izvesna mala razlika u vrednostima E corr.1 kao funkcija osobina pasivnog sloja. Dodatak NaCl u određenoj meri ubrzava reakciju izdvajanja vodonika na pasiviranoj površini, dok NaCl nema uticaja na istu reakciju na goloj površini Cr. Sa druge strane prisustvo NaCl ubrzava anodnu reakciju na goloj površini hroma i aktivira rastvaranje pasivnog sloja, tako da se struja pasivacije povećava sa dodatkom NaCl. Uticaj NaCl je toliko veliki, da pri koncentracijama većim od 3M, razaranje pasivnog sloja postaje brzo, da se Cr za vreme od nekoliko sekundi aktivira i tada se uočava samo jedan stabilni korozioni potencijal E corr.2 . Nije uočena pojava pitinga u prisustvu NaCl, sve do potencijala u transpasivnoj oblasti.",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions, Uticaj hloridnih jona na potencijal otvorenog kola hroma u deaerisanim rastvorima sumporne kiseline",
volume = "71",
number = "11",
pages = "1187-1194",
doi = "10.2298/JSC0611187J"
}
Jegdić, B., Dražić, D. M.,& Popić, J. P.. (2006). Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 71(11), 1187-1194.
https://doi.org/10.2298/JSC0611187J
Jegdić B, Dražić DM, Popić JP. Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions. in Journal of the Serbian Chemical Society. 2006;71(11):1187-1194.
doi:10.2298/JSC0611187J .
Jegdić, Bore, Dražić, Dragutin M., Popić, Jovan P., "Influence of chloride ions on the open circuit potentials of chromium in deaerated sulfuric acid solutions" in Journal of the Serbian Chemical Society, 71, no. 11 (2006):1187-1194,
https://doi.org/10.2298/JSC0611187J . .
1
2
2

Influence of the structure of metallic chromium on its electrochemical and chemical corrosion

Dražić, Dragutin M.; Jegdić, Bore; Popić, Jovan P.

(Belgrade, Serbia : Engineering Society for Corrosion, 2005)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Jegdić, Bore
AU  - Popić, Jovan P.
PY  - 2005
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/198
AB  - It was shown that metallic chromium in aqueous solution of sulfuric acid dissolves in accord with the electrochemical mechanism proposed by Wagner and Traud, but also by a direct chemical reaction of metal with water molecules from the electrolyte, as proposed by Kolotyrkin and coworkers. The experiments in this study were carried out with three different chromium samples: large grain size cast chromium obtained from Merck Co., Germany fine grain metallic chromium rods, obtained from Goodfellows, Pa, USA, and a 121 џт thick electroplated layer of chromium on steel. It was shown that the rates of electrochemical and chemical corrosion are close to each other and similar on all three materials, while on the electroplated chromium surfaces anodic dissolution was ca. 5 times faster than on other chromium surfaces while catholic hydrogen evolution was ca. 5 times slower than on other chromium surfaces. These differences are obviously the consequences of the differences in the structure of electroplated chromium as contrasted to the other chromium samples. This conclusion is supported by the results obtained with the samples with two large crystal grains of different structure and orientation.
AB  - Pokazano je da se u vodenim rastvorima sumporne kiseline metalni hrom rastvara elektrohemijskim mehanizmom u skladu sa modelom Vaguera i Trauda ali da se hrom paralelno rastvara i hemijskim mehanizmom po modelu Kolotirkina i saradnika direktnim reagovanjem metala sa molekulima vode iz rastvora. Kao materijal za ispitivanje služio je krupnozrni liveni hrom sitnozrni kovani i valjani hrom i elektrolitički istaložena hromna prevlaka. Pokazano je da su brzine elektrohemijske i hemijske korozije međusobno slične kod sva tri materijala, dok je elektrohemijska prevlaka imala oko 5 puta bržu anodnu reakciju i skoro 5 puta sporiju katodnu reakciju izdvajanja vodonika. Ove razlike posledica su svakako razlika u strukturi i kristalografskoj orijentaciji hromne prevlake prema rastvoru, što se u izvesnoj meri uočava i na primeru krupnozrne livene strukture, gde dva različita velika zrna imaju određene razlike u brzinama ovih elektrohemijskih reakcija, iako u znatno manjoj meri.
PB  - Belgrade, Serbia : Engineering Society for Corrosion
T2  - Zaštita materijala
T1  - Influence of the structure of metallic chromium on its electrochemical and chemical corrosion
T1  - Uticaj strukture metalnog hroma na njegovu elektrohemijsku i hemijsku koroziju
VL  - 46
IS  - 2
SP  - 29
EP  - 34
UR  - https://hdl.handle.net/21.15107/rcub_cer_198
ER  - 
@article{
author = "Dražić, Dragutin M. and Jegdić, Bore and Popić, Jovan P.",
year = "2005",
abstract = "It was shown that metallic chromium in aqueous solution of sulfuric acid dissolves in accord with the electrochemical mechanism proposed by Wagner and Traud, but also by a direct chemical reaction of metal with water molecules from the electrolyte, as proposed by Kolotyrkin and coworkers. The experiments in this study were carried out with three different chromium samples: large grain size cast chromium obtained from Merck Co., Germany fine grain metallic chromium rods, obtained from Goodfellows, Pa, USA, and a 121 џт thick electroplated layer of chromium on steel. It was shown that the rates of electrochemical and chemical corrosion are close to each other and similar on all three materials, while on the electroplated chromium surfaces anodic dissolution was ca. 5 times faster than on other chromium surfaces while catholic hydrogen evolution was ca. 5 times slower than on other chromium surfaces. These differences are obviously the consequences of the differences in the structure of electroplated chromium as contrasted to the other chromium samples. This conclusion is supported by the results obtained with the samples with two large crystal grains of different structure and orientation., Pokazano je da se u vodenim rastvorima sumporne kiseline metalni hrom rastvara elektrohemijskim mehanizmom u skladu sa modelom Vaguera i Trauda ali da se hrom paralelno rastvara i hemijskim mehanizmom po modelu Kolotirkina i saradnika direktnim reagovanjem metala sa molekulima vode iz rastvora. Kao materijal za ispitivanje služio je krupnozrni liveni hrom sitnozrni kovani i valjani hrom i elektrolitički istaložena hromna prevlaka. Pokazano je da su brzine elektrohemijske i hemijske korozije međusobno slične kod sva tri materijala, dok je elektrohemijska prevlaka imala oko 5 puta bržu anodnu reakciju i skoro 5 puta sporiju katodnu reakciju izdvajanja vodonika. Ove razlike posledica su svakako razlika u strukturi i kristalografskoj orijentaciji hromne prevlake prema rastvoru, što se u izvesnoj meri uočava i na primeru krupnozrne livene strukture, gde dva različita velika zrna imaju određene razlike u brzinama ovih elektrohemijskih reakcija, iako u znatno manjoj meri.",
publisher = "Belgrade, Serbia : Engineering Society for Corrosion",
journal = "Zaštita materijala",
title = "Influence of the structure of metallic chromium on its electrochemical and chemical corrosion, Uticaj strukture metalnog hroma na njegovu elektrohemijsku i hemijsku koroziju",
volume = "46",
number = "2",
pages = "29-34",
url = "https://hdl.handle.net/21.15107/rcub_cer_198"
}
Dražić, D. M., Jegdić, B.,& Popić, J. P.. (2005). Influence of the structure of metallic chromium on its electrochemical and chemical corrosion. in Zaštita materijala
Belgrade, Serbia : Engineering Society for Corrosion., 46(2), 29-34.
https://hdl.handle.net/21.15107/rcub_cer_198
Dražić DM, Jegdić B, Popić JP. Influence of the structure of metallic chromium on its electrochemical and chemical corrosion. in Zaštita materijala. 2005;46(2):29-34.
https://hdl.handle.net/21.15107/rcub_cer_198 .
Dražić, Dragutin M., Jegdić, Bore, Popić, Jovan P., "Influence of the structure of metallic chromium on its electrochemical and chemical corrosion" in Zaštita materijala, 46, no. 2 (2005):29-34,
https://hdl.handle.net/21.15107/rcub_cer_198 .

Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid

Dražić, Dragutin M.; Popić, Jovan P.; Jegdić, Bore; Vasiljević-Radović, Dana

(Serbian Chemical Society, 2004)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
AU  - Jegdić, Bore
AU  - Vasiljević-Radović, Dana
PY  - 2004
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/144
AB  - Chromium dissolution in aqueous sulfuric acid solutions in the pH range 0.5 –3 was studied electrochemically by the potentiostatic or very slow potentiodynamic method, and by the analyses of the Cr ion concentrations in the electrolyte formed during the experiments. It was shown that the electrochemical anodic dissolution follows a common Tafel line with a slope of ca. 120 mVdec-1, independent of the solution pH and the hydrodynamics while the passivation potentials and passivation currents were independent on hydrodynamics but strongly dependent on the pH. In parallel with the electrochemical dissolution, a considerable "anomalous" or chemical Cr dissolution process occurs, as evidenced by the spectrophotometric analyses of the electrolytes for Cr ions after prolonged potentiostating of the electrodes at different potentials, as well as by measuring the electrode weight losses. All these results indicate the existence of a potential independent reaction of Cr dissolution occurring in parallel to the anodic dissolution process. Mechanisms for both the electrochemical and the chemical process are proposed. The consequences of these phenomena on the behavior of some practical systems where chromium or a chromium alloy (e.g., stainless steels) are used are discussed.
AB  - Proučavano je anodno rastvaranje hroma u vodenim rastvorima sumporne kiseline u oblasti pH 0,5 – 3 potenciostatskom i vrlo sporom potenciodinamičkom metodom, kao i analitičkim praćenjem promene koncentracije Cr jona tokom eksperimenata. Pokazano je da elektrohemijsko anodno rastvaranje prati uobičajeno Tafelovo ponašanje sa nagibom Tafelove prave od oko 120 mV dec-1 kao i da je nezavisno od pH i hidrodinamike. Međutim, potencijali pasivacije i struje pasivacije takođe su nezavisni od hidrodinamike, ali vrlo zavisne od pH. Jednovremeno sa elektrohemijskim rastvaranjem odigrava se i značajno "anomalno" ili hemijsko rastvaranje hroma. Ovo je potvrđeno i spektrofotometrijskim analizama rastvora tokom dužeg potenciostatskog održavanja katodnih i anodnih polarizacija, kao i merenjem gubitka mase elektrode. Svi ovi rezultati ukazuju na odigravanje nezavisne reakcije rastvaranja hroma koja nije zavisna od potencijala, kao što je slučaj sa elektrohemijskom reakcijom. Predloženi su mehanizmi odigravanja oba navedena procesa. Razmotrene su i posledice postojanja oba navedenafenomena na ponašanje nekih praktičnih sistema u kojima se koristi hrom ili legure hroma (npr. nerđajući čelik).
PB  - Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid
T1  - Elektrohemija aktivnog hroma, deo IV - rastvaranje hroma u deaeriranom vodenom rastvoru sumporne kiseline
VL  - 69
IS  - 12
SP  - 1099
EP  - 1110
DO  - 10.2298/JSC0412099D
ER  - 
@article{
author = "Dražić, Dragutin M. and Popić, Jovan P. and Jegdić, Bore and Vasiljević-Radović, Dana",
year = "2004",
abstract = "Chromium dissolution in aqueous sulfuric acid solutions in the pH range 0.5 –3 was studied electrochemically by the potentiostatic or very slow potentiodynamic method, and by the analyses of the Cr ion concentrations in the electrolyte formed during the experiments. It was shown that the electrochemical anodic dissolution follows a common Tafel line with a slope of ca. 120 mVdec-1, independent of the solution pH and the hydrodynamics while the passivation potentials and passivation currents were independent on hydrodynamics but strongly dependent on the pH. In parallel with the electrochemical dissolution, a considerable "anomalous" or chemical Cr dissolution process occurs, as evidenced by the spectrophotometric analyses of the electrolytes for Cr ions after prolonged potentiostating of the electrodes at different potentials, as well as by measuring the electrode weight losses. All these results indicate the existence of a potential independent reaction of Cr dissolution occurring in parallel to the anodic dissolution process. Mechanisms for both the electrochemical and the chemical process are proposed. The consequences of these phenomena on the behavior of some practical systems where chromium or a chromium alloy (e.g., stainless steels) are used are discussed., Proučavano je anodno rastvaranje hroma u vodenim rastvorima sumporne kiseline u oblasti pH 0,5 – 3 potenciostatskom i vrlo sporom potenciodinamičkom metodom, kao i analitičkim praćenjem promene koncentracije Cr jona tokom eksperimenata. Pokazano je da elektrohemijsko anodno rastvaranje prati uobičajeno Tafelovo ponašanje sa nagibom Tafelove prave od oko 120 mV dec-1 kao i da je nezavisno od pH i hidrodinamike. Međutim, potencijali pasivacije i struje pasivacije takođe su nezavisni od hidrodinamike, ali vrlo zavisne od pH. Jednovremeno sa elektrohemijskim rastvaranjem odigrava se i značajno "anomalno" ili hemijsko rastvaranje hroma. Ovo je potvrđeno i spektrofotometrijskim analizama rastvora tokom dužeg potenciostatskog održavanja katodnih i anodnih polarizacija, kao i merenjem gubitka mase elektrode. Svi ovi rezultati ukazuju na odigravanje nezavisne reakcije rastvaranja hroma koja nije zavisna od potencijala, kao što je slučaj sa elektrohemijskom reakcijom. Predloženi su mehanizmi odigravanja oba navedena procesa. Razmotrene su i posledice postojanja oba navedenafenomena na ponašanje nekih praktičnih sistema u kojima se koristi hrom ili legure hroma (npr. nerđajući čelik).",
publisher = "Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid, Elektrohemija aktivnog hroma, deo IV - rastvaranje hroma u deaeriranom vodenom rastvoru sumporne kiseline",
volume = "69",
number = "12",
pages = "1099-1110",
doi = "10.2298/JSC0412099D"
}
Dražić, D. M., Popić, J. P., Jegdić, B.,& Vasiljević-Radović, D.. (2004). Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid. in Journal of the Serbian Chemical Society
Serbian Chemical Society., 69(12), 1099-1110.
https://doi.org/10.2298/JSC0412099D
Dražić DM, Popić JP, Jegdić B, Vasiljević-Radović D. Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid. in Journal of the Serbian Chemical Society. 2004;69(12):1099-1110.
doi:10.2298/JSC0412099D .
Dražić, Dragutin M., Popić, Jovan P., Jegdić, Bore, Vasiljević-Radović, Dana, "Electrochemistry of active chromium, part IV: Dissolution of chromium in deaerated sulfuric acid" in Journal of the Serbian Chemical Society, 69, no. 12 (2004):1099-1110,
https://doi.org/10.2298/JSC0412099D . .
6
7
4

Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy

Bajat, Jelena; Mišković-Stanković, Vesna; Maksimović, Miodrag D.; Dražić, Dragutin M.; Zec, Slavica

(Elsevier, 2002)

TY  - JOUR
AU  - Bajat, Jelena
AU  - Mišković-Stanković, Vesna
AU  - Maksimović, Miodrag D.
AU  - Dražić, Dragutin M.
AU  - Zec, Slavica
PY  - 2002
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4108
AB  - Zn-Co alloys electrochemically deposited on steel under various deposition conditions were investigated. The influence of deposition current density, temperature and composition of deposition solution on the phase structure and corrosion properties of Zn-Co alloys were studied. It was found that Zn-Co alloy obtained from chloride solution at 5 A dm-2 showed the best corrosion properties, so this alloy was chosen for further examination. Epoxy coating was electrodeposited on steel and steel modified by Zn-Co alloy using constant voltage method. The effect of Zn-Co alloy on the corrosion behavior of the protective system based on epoxy coating is interpreted in terms of electrochemical and transport properties, as well as of thermal stability.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy
VL  - 47
IS  - 25
SP  - 4101
EP  - 4112
DO  - 10.1016/S0013-4686(02)00418-8
ER  - 
@article{
author = "Bajat, Jelena and Mišković-Stanković, Vesna and Maksimović, Miodrag D. and Dražić, Dragutin M. and Zec, Slavica",
year = "2002",
abstract = "Zn-Co alloys electrochemically deposited on steel under various deposition conditions were investigated. The influence of deposition current density, temperature and composition of deposition solution on the phase structure and corrosion properties of Zn-Co alloys were studied. It was found that Zn-Co alloy obtained from chloride solution at 5 A dm-2 showed the best corrosion properties, so this alloy was chosen for further examination. Epoxy coating was electrodeposited on steel and steel modified by Zn-Co alloy using constant voltage method. The effect of Zn-Co alloy on the corrosion behavior of the protective system based on epoxy coating is interpreted in terms of electrochemical and transport properties, as well as of thermal stability.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy",
volume = "47",
number = "25",
pages = "4101-4112",
doi = "10.1016/S0013-4686(02)00418-8"
}
Bajat, J., Mišković-Stanković, V., Maksimović, M. D., Dražić, D. M.,& Zec, S.. (2002). Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy. in Electrochimica Acta
Elsevier., 47(25), 4101-4112.
https://doi.org/10.1016/S0013-4686(02)00418-8
Bajat J, Mišković-Stanković V, Maksimović MD, Dražić DM, Zec S. Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy. in Electrochimica Acta. 2002;47(25):4101-4112.
doi:10.1016/S0013-4686(02)00418-8 .
Bajat, Jelena, Mišković-Stanković, Vesna, Maksimović, Miodrag D., Dražić, Dragutin M., Zec, Slavica, "Electrochemical deposition and characterization of Zn /Co alloys and corrosion protection by electrodeposited epoxy coating on Zn /Co alloy" in Electrochimica Acta, 47, no. 25 (2002):4101-4112,
https://doi.org/10.1016/S0013-4686(02)00418-8 . .
62
66
69

Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid

Vračar, Ljubomir; Dražić, Dragutin M.

(Elsevier, 2002)

TY  - JOUR
AU  - Vračar, Ljubomir
AU  - Dražić, Dragutin M.
PY  - 2002
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4090
AB  - Adsorption and corrosion inhibitive properties of three different organic molecules: 2-naphthalenesulfonic acid, 2,7-naphthalenedisulfonic acid and 2-naphthol-3,6-disulfonic acid are investigated on Armco-iron electrode cathodically polarized, in 0.5 mol dm -3 H 2 SO 4 solution. The examinations show that the three organic molecules behave as a cathodic corrosion inhibitors. The inhibitive efficiency, changes with the number of functional groups substituted on benzene ring and increases with concentration. The experimentally obtained adsorption isoterms follow the Frumkin equation [0/n(1-0) n ] exp(-2aθ) = Bc and the best fit is obtained for n = 2 (for 2-NSA) and n = 3 (for 2,7-NDSA and 2N-3,6-DSA). The calculated values for the parameter a are 2.1-2.9 and Gibbs energies are 17-21 kJ mol -1 . The adsorption rate constants are very small, proving that iron surface permanently changes due to the corrosion processes.
PB  - Elsevier
T2  - Corrosion Science
T1  - Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid
VL  - 44
IS  - 8
SP  - 1669
EP  - 1680
DO  - 10.1016/S0010-938X(01)00166-4
ER  - 
@article{
author = "Vračar, Ljubomir and Dražić, Dragutin M.",
year = "2002",
abstract = "Adsorption and corrosion inhibitive properties of three different organic molecules: 2-naphthalenesulfonic acid, 2,7-naphthalenedisulfonic acid and 2-naphthol-3,6-disulfonic acid are investigated on Armco-iron electrode cathodically polarized, in 0.5 mol dm -3 H 2 SO 4 solution. The examinations show that the three organic molecules behave as a cathodic corrosion inhibitors. The inhibitive efficiency, changes with the number of functional groups substituted on benzene ring and increases with concentration. The experimentally obtained adsorption isoterms follow the Frumkin equation [0/n(1-0) n ] exp(-2aθ) = Bc and the best fit is obtained for n = 2 (for 2-NSA) and n = 3 (for 2,7-NDSA and 2N-3,6-DSA). The calculated values for the parameter a are 2.1-2.9 and Gibbs energies are 17-21 kJ mol -1 . The adsorption rate constants are very small, proving that iron surface permanently changes due to the corrosion processes.",
publisher = "Elsevier",
journal = "Corrosion Science",
title = "Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid",
volume = "44",
number = "8",
pages = "1669-1680",
doi = "10.1016/S0010-938X(01)00166-4"
}
Vračar, L.,& Dražić, D. M.. (2002). Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid. in Corrosion Science
Elsevier., 44(8), 1669-1680.
https://doi.org/10.1016/S0010-938X(01)00166-4
Vračar L, Dražić DM. Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid. in Corrosion Science. 2002;44(8):1669-1680.
doi:10.1016/S0010-938X(01)00166-4 .
Vračar, Ljubomir, Dražić, Dragutin M., "Adsorption and corrosion inhibitive properties of some organic molecules on iron electrode in sulfuric acid" in Corrosion Science, 44, no. 8 (2002):1669-1680,
https://doi.org/10.1016/S0010-938X(01)00166-4 . .
253
232
295

Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver

Jović, Borka M.; Dražić, Dragutin M.; Jović, Vladimir D.

(Belgrade : Serbian Chemical Society, 1999)

TY  - JOUR
AU  - Jović, Borka M.
AU  - Dražić, Dragutin M.
AU  - Jović, Vladimir D.
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4410
AB  - The processes of adsorption of sulphate anions onto the (111) face of silver have been investigated by analysis of the cyclic voltammetry and potcntiostatic pulse results. It was shown, by fitting the experimentally recorded θ - E dependences, that the adsorption of anions follows Frumkin adsorption isotherm. The adsorbed structure was found to be less dense than expected for the dense packed anion monolayer and the process was characterized by high value of the interaction parameter and the Gibbs energy of adsorption (f = 16.5 and ΔGoads.θ→0 = - 64 kJ mol 1). From the slope of the Ep.a - log (c0) dependence it was concluded that complete charge transfer between the adsorbed anions and the silver substrate occurs. This is supported by the Ep.a - log v linear dependence in the region of high sweep rates (v > 10 V s 1) with rational value of line slope (≈ 60 mV dec 1) which is possible only if the complete charge transfer reaction occurs. The elcctrosorption process of sulphate anions was found to be complex electrochemical reaction, taking place through three steps. It was proposed that the rate-determining step is the second step, i.e., the electrochemical formation of (SO4)ads species.
AB  - Proučavan je proces adsorpcije sulfatnih anjona na (111) pljosni monokristala
srebra metodama ciklične voltametrije i potenciostatskih pulseva. Na osnovu eksperimentalno određenih q–E zavisnosti pokazano je da se na adsorpciju može primeniti Frumkinova adsorpciona izoterma. Nađeno je da je gustina adsorbovanog sloja
manja nego kada bi sloj bio maksimalno moguće gusto pakovan kao i da adsorpciju
karakterišu visoke vrednosti Frumkinovog parametra interakcije (f = 16,5) i Gibsove
energije adosrpcije (DGºads,q®0 = –64 kJ mol). Na osnovu nagiba zavisnosti Ep,a –log (c0)
zaključeno je da se pri elektrosorpciji odigrava i potpuna izmena naboja anjona sa
supstratom. Ovaj zaključak podržava dobijena linearna zavisnost Ep,a – log v u oblasti
velikih brzina promene potencijala (v>10 V s–1) sa racionalnom vrednošću nagiba (»60
mV dek–1), a koja se može dobiti samo pri odigravanju potpune razmene naboja. Utvrđeno
je da je elektrosorpcija sulfatnih anjona složena elektrohemijska reakcija koja se
odigrava u tri stupnja. Stupanj koji određuje brzinu ukupne reakcije je drugi stupanj,
elektrohemijsko stvaranje intermedijera (SO4)ads.
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver
T1  - Mehanizam i kinetika elektrosorpcije sulfatnih anjona na (111) pljosni srebra
VL  - 64
IS  - 9
SP  - 539
EP  - 552
DO  - 10.2298/jsc9909539j
ER  - 
@article{
author = "Jović, Borka M. and Dražić, Dragutin M. and Jović, Vladimir D.",
year = "1999",
abstract = "The processes of adsorption of sulphate anions onto the (111) face of silver have been investigated by analysis of the cyclic voltammetry and potcntiostatic pulse results. It was shown, by fitting the experimentally recorded θ - E dependences, that the adsorption of anions follows Frumkin adsorption isotherm. The adsorbed structure was found to be less dense than expected for the dense packed anion monolayer and the process was characterized by high value of the interaction parameter and the Gibbs energy of adsorption (f = 16.5 and ΔGoads.θ→0 = - 64 kJ mol 1). From the slope of the Ep.a - log (c0) dependence it was concluded that complete charge transfer between the adsorbed anions and the silver substrate occurs. This is supported by the Ep.a - log v linear dependence in the region of high sweep rates (v > 10 V s 1) with rational value of line slope (≈ 60 mV dec 1) which is possible only if the complete charge transfer reaction occurs. The elcctrosorption process of sulphate anions was found to be complex electrochemical reaction, taking place through three steps. It was proposed that the rate-determining step is the second step, i.e., the electrochemical formation of (SO4)ads species., Proučavan je proces adsorpcije sulfatnih anjona na (111) pljosni monokristala
srebra metodama ciklične voltametrije i potenciostatskih pulseva. Na osnovu eksperimentalno određenih q–E zavisnosti pokazano je da se na adsorpciju može primeniti Frumkinova adsorpciona izoterma. Nađeno je da je gustina adsorbovanog sloja
manja nego kada bi sloj bio maksimalno moguće gusto pakovan kao i da adsorpciju
karakterišu visoke vrednosti Frumkinovog parametra interakcije (f = 16,5) i Gibsove
energije adosrpcije (DGºads,q®0 = –64 kJ mol). Na osnovu nagiba zavisnosti Ep,a –log (c0)
zaključeno je da se pri elektrosorpciji odigrava i potpuna izmena naboja anjona sa
supstratom. Ovaj zaključak podržava dobijena linearna zavisnost Ep,a – log v u oblasti
velikih brzina promene potencijala (v>10 V s–1) sa racionalnom vrednošću nagiba (»60
mV dek–1), a koja se može dobiti samo pri odigravanju potpune razmene naboja. Utvrđeno
je da je elektrosorpcija sulfatnih anjona složena elektrohemijska reakcija koja se
odigrava u tri stupnja. Stupanj koji određuje brzinu ukupne reakcije je drugi stupanj,
elektrohemijsko stvaranje intermedijera (SO4)ads.",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver, Mehanizam i kinetika elektrosorpcije sulfatnih anjona na (111) pljosni srebra",
volume = "64",
number = "9",
pages = "539-552",
doi = "10.2298/jsc9909539j"
}
Jović, B. M., Dražić, D. M.,& Jović, V. D.. (1999). Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 64(9), 539-552.
https://doi.org/10.2298/jsc9909539j
Jović BM, Dražić DM, Jović VD. Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver. in Journal of the Serbian Chemical Society. 1999;64(9):539-552.
doi:10.2298/jsc9909539j .
Jović, Borka M., Dražić, Dragutin M., Jović, Vladimir D., "Mechanism and kinetics of the electrosorption of sulphate anions on the (111) face of silver" in Journal of the Serbian Chemical Society, 64, no. 9 (1999):539-552,
https://doi.org/10.2298/jsc9909539j . .
2
3

Corrosion protection of aluminium by a cataphoretic epoxy coating

Mišković-Stanković, Vesna; Stanić, M.R.; Dražić, Dragutin M.

(Elsevier, 1999)

TY  - JOUR
AU  - Mišković-Stanković, Vesna
AU  - Stanić, M.R.
AU  - Dražić, Dragutin M.
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4053
AB  - The corrosion behavior and thermal stability of epoxy coating electrodeposited on aluminium have been investigated during exposure to
3% NaCl. Electrochemical impedance spectroscopy (EIS), gravimetric liquid sorption experiments, thermogravimetric analysis (TGA) and
polarization measurements were used. From the results obtained from EIS (pore resistance, coating capacitance, relative permittivity of
coating, charge-transfer resistance, double-layer capacitance), gravimetric liquid sorption experiments (diffusion coef®cient, energy of
activation of water diffusion) and TGA (water content inside the coating and thermal stability), it can be concluded that the electrochemical,
transport and thermal properties of an epoxy coating on aluminium are signi®cantly improved with respect to the same epoxy coating on
other substrates (steel, phosphatized steel, steel modi®ed by Zn±Ni alloy). The better protective properties can be explained by less porous
structure of the coating on aluminium, caused by lower rate of H2 evolution, while the prolonged corrosion protection is due to the passive,
mainly barrier ®lm of Al2O3 on its surface.
PB  - Elsevier
T2  - Progress in Organic Coatings
T1  - Corrosion protection of aluminium by a cataphoretic epoxy coating
VL  - 36
IS  - 1-2
SP  - 53
EP  - 63
DO  - 10.1016/S0300-9440(99)00024-7
ER  - 
@article{
author = "Mišković-Stanković, Vesna and Stanić, M.R. and Dražić, Dragutin M.",
year = "1999",
abstract = "The corrosion behavior and thermal stability of epoxy coating electrodeposited on aluminium have been investigated during exposure to
3% NaCl. Electrochemical impedance spectroscopy (EIS), gravimetric liquid sorption experiments, thermogravimetric analysis (TGA) and
polarization measurements were used. From the results obtained from EIS (pore resistance, coating capacitance, relative permittivity of
coating, charge-transfer resistance, double-layer capacitance), gravimetric liquid sorption experiments (diffusion coef®cient, energy of
activation of water diffusion) and TGA (water content inside the coating and thermal stability), it can be concluded that the electrochemical,
transport and thermal properties of an epoxy coating on aluminium are signi®cantly improved with respect to the same epoxy coating on
other substrates (steel, phosphatized steel, steel modi®ed by Zn±Ni alloy). The better protective properties can be explained by less porous
structure of the coating on aluminium, caused by lower rate of H2 evolution, while the prolonged corrosion protection is due to the passive,
mainly barrier ®lm of Al2O3 on its surface.",
publisher = "Elsevier",
journal = "Progress in Organic Coatings",
title = "Corrosion protection of aluminium by a cataphoretic epoxy coating",
volume = "36",
number = "1-2",
pages = "53-63",
doi = "10.1016/S0300-9440(99)00024-7"
}
Mišković-Stanković, V., Stanić, M.R.,& Dražić, D. M.. (1999). Corrosion protection of aluminium by a cataphoretic epoxy coating. in Progress in Organic Coatings
Elsevier., 36(1-2), 53-63.
https://doi.org/10.1016/S0300-9440(99)00024-7
Mišković-Stanković V, Stanić M, Dražić DM. Corrosion protection of aluminium by a cataphoretic epoxy coating. in Progress in Organic Coatings. 1999;36(1-2):53-63.
doi:10.1016/S0300-9440(99)00024-7 .
Mišković-Stanković, Vesna, Stanić, M.R., Dražić, Dragutin M., "Corrosion protection of aluminium by a cataphoretic epoxy coating" in Progress in Organic Coatings, 36, no. 1-2 (1999):53-63,
https://doi.org/10.1016/S0300-9440(99)00024-7 . .
81
64
85

Real surface area of the aluminium electrode in sodium chloride solution

Dražić, Dragutin M.; Popić, Jovan P.; Rakočević, Zlatko Lj.

(Belgrade : Serbian Chemical Society, 1999)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan P.
AU  - Rakočević, Zlatko Lj.
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4397
AB  - By combining the techniques of electrochemical slow potentiodynamic, AC impedance and atomic force microscopy (AFM), it was shown that the differences in the anodic dissolution rates of Al in 0.5 NaCl solutions as measured experimentally in the potential region between the corrosion and pitting potential, are mainly due to differences in surface roughness of the electrodes used. It was shown that mechanical grinding and polishing of the electrode surface with emery paper (400 grit) and alumina polishing powder ((Latin small letter o with stroke) 0.25 μm) can produce surfaces differing by a factor of 6 in the roughness factor Ra. By using AFM estimates of the roughness factors a true electrode capacitance of 4.63 μC cm-2 and thickness dox ≈ 2.0 nm for the barrier layer of the surface film was estamited. The outer part of the film is porous, partly as amorphous A1(OH)3, or crystalline bayerite (Al2O3-3H2O).
AB  - Pokazano je, kombinovanim korišćenjem tehnika spore potenciodinamike, AC impedance i atomske mikroskopije (AFM), da su razlike u brzinama anodnog rastvarača Al u 0,5 M NaCl u oblasti između korozionog i piting potencijala, a koje se zapažaju u eksperimentima, prvenstveno posledica razlike u površinskoj hrapavosti različito pripremljenih elektroda. Pokazano je da se mehaničkim brušenjem (finoća 400) i poliranjem Al2O3 pastom (0,25 mm) dobija razlika faktora hrapavosti za oko 6 puta. Uz pomoć AFM tehnike za određivanje faktora hrapavosti procenjena je prava kapacitivnost elektroda od 4,63 mF cm–2 i debljina barijernog sloja oksida od dox ≈ 2,0 nm. Spoljašnji porozni sloj je delimično amorfan Al(OH)3 ili kristalinični bajerit (Al2O3.3H2O).
PB  - Belgrade : Serbian Chemical Society
T2  - Journal of the Serbian Chemical Society
T1  - Real surface area of the aluminium electrode in sodium chloride solution
T1  - Stvarna površina eletrode od aluminijuma u rastvoru natrijum-hlorida
VL  - 64
IS  - 11
SP  - 685
EP  - 685
DO  - 10.2298/jsc9911685d
ER  - 
@article{
author = "Dražić, Dragutin M. and Popić, Jovan P. and Rakočević, Zlatko Lj.",
year = "1999",
abstract = "By combining the techniques of electrochemical slow potentiodynamic, AC impedance and atomic force microscopy (AFM), it was shown that the differences in the anodic dissolution rates of Al in 0.5 NaCl solutions as measured experimentally in the potential region between the corrosion and pitting potential, are mainly due to differences in surface roughness of the electrodes used. It was shown that mechanical grinding and polishing of the electrode surface with emery paper (400 grit) and alumina polishing powder ((Latin small letter o with stroke) 0.25 μm) can produce surfaces differing by a factor of 6 in the roughness factor Ra. By using AFM estimates of the roughness factors a true electrode capacitance of 4.63 μC cm-2 and thickness dox ≈ 2.0 nm for the barrier layer of the surface film was estamited. The outer part of the film is porous, partly as amorphous A1(OH)3, or crystalline bayerite (Al2O3-3H2O)., Pokazano je, kombinovanim korišćenjem tehnika spore potenciodinamike, AC impedance i atomske mikroskopije (AFM), da su razlike u brzinama anodnog rastvarača Al u 0,5 M NaCl u oblasti između korozionog i piting potencijala, a koje se zapažaju u eksperimentima, prvenstveno posledica razlike u površinskoj hrapavosti različito pripremljenih elektroda. Pokazano je da se mehaničkim brušenjem (finoća 400) i poliranjem Al2O3 pastom (0,25 mm) dobija razlika faktora hrapavosti za oko 6 puta. Uz pomoć AFM tehnike za određivanje faktora hrapavosti procenjena je prava kapacitivnost elektroda od 4,63 mF cm–2 i debljina barijernog sloja oksida od dox ≈ 2,0 nm. Spoljašnji porozni sloj je delimično amorfan Al(OH)3 ili kristalinični bajerit (Al2O3.3H2O).",
publisher = "Belgrade : Serbian Chemical Society",
journal = "Journal of the Serbian Chemical Society",
title = "Real surface area of the aluminium electrode in sodium chloride solution, Stvarna površina eletrode od aluminijuma u rastvoru natrijum-hlorida",
volume = "64",
number = "11",
pages = "685-685",
doi = "10.2298/jsc9911685d"
}
Dražić, D. M., Popić, J. P.,& Rakočević, Z. Lj.. (1999). Real surface area of the aluminium electrode in sodium chloride solution. in Journal of the Serbian Chemical Society
Belgrade : Serbian Chemical Society., 64(11), 685-685.
https://doi.org/10.2298/jsc9911685d
Dražić DM, Popić JP, Rakočević ZL. Real surface area of the aluminium electrode in sodium chloride solution. in Journal of the Serbian Chemical Society. 1999;64(11):685-685.
doi:10.2298/jsc9911685d .
Dražić, Dragutin M., Popić, Jovan P., Rakočević, Zlatko Lj., "Real surface area of the aluminium electrode in sodium chloride solution" in Journal of the Serbian Chemical Society, 64, no. 11 (1999):685-685,
https://doi.org/10.2298/jsc9911685d . .
2
2

Corrosion rates and negative difference effects for Al and some Al alloys

Dražić, Dragutin M.; Popić, Jovan

(Springer, 1999)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Popić, Jovan
PY  - 1999
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4082
AB  - The rotating disc-ring technique with a Pt ring was used to quantitatively detect hydrogen evolved on an Al-disc electrode during spontaneous corrosion at open-circuit potential or during anodic polarization of an Al disc to study the unusual increase of H2 evolution with increase in anodic current (the so called negative difference effect). Experiments were made with high purity Al (99.999%), technical grade Al (99.5%) (Al–T) and Al–In alloy (0.074% In) in deaerated 0.5m aqueous NaCl solution (pH∼6.5) and NaCl solutions acidified with HCl to pH values of 3.0, 2.0 and 1.0. It was shown, in neutral solutions, that the corrosion rates of all three materials are controlled by the rate of water molecule dissociation or in more acid solutions, by the combined water molecule dissociation rate and H+ ion discharge rate. The corrosion rates of all three materials in the range of 3–10μAcm2, was the lowest for 99.999% Al. The impurities in Al–T and Al–In increase the hydrogen evolution rate at cathodic polarizations in a similar manner, but very differently affect the negative difference effect. High purity Al and Al–T have a similar negative difference effect (8–15%), while the presence of In decreases it to only about 1%. No pitting and no negative difference effect were observed at potentials more negative than Epit. Therefore, the negative difference effect is connected with the anodic pitting dissolution mechanism. Several aspects of this problem are discussed in more detail.
PB  - Springer
T2  - Journal of Applied Electrochemistry
T1  - Corrosion rates and negative difference effects for Al and some Al alloys
VL  - 29
SP  - 43
EP  - 50
DO  - 10.1023/A:1003447018115
ER  - 
@article{
author = "Dražić, Dragutin M. and Popić, Jovan",
year = "1999",
abstract = "The rotating disc-ring technique with a Pt ring was used to quantitatively detect hydrogen evolved on an Al-disc electrode during spontaneous corrosion at open-circuit potential or during anodic polarization of an Al disc to study the unusual increase of H2 evolution with increase in anodic current (the so called negative difference effect). Experiments were made with high purity Al (99.999%), technical grade Al (99.5%) (Al–T) and Al–In alloy (0.074% In) in deaerated 0.5m aqueous NaCl solution (pH∼6.5) and NaCl solutions acidified with HCl to pH values of 3.0, 2.0 and 1.0. It was shown, in neutral solutions, that the corrosion rates of all three materials are controlled by the rate of water molecule dissociation or in more acid solutions, by the combined water molecule dissociation rate and H+ ion discharge rate. The corrosion rates of all three materials in the range of 3–10μAcm2, was the lowest for 99.999% Al. The impurities in Al–T and Al–In increase the hydrogen evolution rate at cathodic polarizations in a similar manner, but very differently affect the negative difference effect. High purity Al and Al–T have a similar negative difference effect (8–15%), while the presence of In decreases it to only about 1%. No pitting and no negative difference effect were observed at potentials more negative than Epit. Therefore, the negative difference effect is connected with the anodic pitting dissolution mechanism. Several aspects of this problem are discussed in more detail.",
publisher = "Springer",
journal = "Journal of Applied Electrochemistry",
title = "Corrosion rates and negative difference effects for Al and some Al alloys",
volume = "29",
pages = "43-50",
doi = "10.1023/A:1003447018115"
}
Dražić, D. M.,& Popić, J.. (1999). Corrosion rates and negative difference effects for Al and some Al alloys. in Journal of Applied Electrochemistry
Springer., 29, 43-50.
https://doi.org/10.1023/A:1003447018115
Dražić DM, Popić J. Corrosion rates and negative difference effects for Al and some Al alloys. in Journal of Applied Electrochemistry. 1999;29:43-50.
doi:10.1023/A:1003447018115 .
Dražić, Dragutin M., Popić, Jovan, "Corrosion rates and negative difference effects for Al and some Al alloys" in Journal of Applied Electrochemistry, 29 (1999):43-50,
https://doi.org/10.1023/A:1003447018115 . .
62
61
66

Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media

Tripković, Amalija; Popović, Ksenija; Momčilović, J. D.; Dražić, Dragutin M.

(Elsevier, 1998)

TY  - JOUR
AU  - Tripković, Amalija
AU  - Popović, Ksenija
AU  - Momčilović, J. D.
AU  - Dražić, Dragutin M.
PY  - 1998
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4163
AB  - A comparative study of methanol oxidation on a Pt(100) surface was carried out in bicarbonate, carbonate and different pH values of sodium hydroxide solutions. It was shown that Pt(100) adsorbs OH and 'poisoning species'. The surface activity was directly correlated to the OHad species coverage. The 'poisoning species', produced in methanol oxidation, participate in the reaction at higher potentials, but block the surface partially at lower potentials. A dual path reaction mechanism, common to all the alkaline solutions used, was proposed based on the assumptions that HCO is a reactive intermediate and that a formate is a reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media
VL  - 448
IS  - 2
SP  - 173
EP  - 181
DO  - 10.1016/S0022-0728(97)00141-1
ER  - 
@article{
author = "Tripković, Amalija and Popović, Ksenija and Momčilović, J. D. and Dražić, Dragutin M.",
year = "1998",
abstract = "A comparative study of methanol oxidation on a Pt(100) surface was carried out in bicarbonate, carbonate and different pH values of sodium hydroxide solutions. It was shown that Pt(100) adsorbs OH and 'poisoning species'. The surface activity was directly correlated to the OHad species coverage. The 'poisoning species', produced in methanol oxidation, participate in the reaction at higher potentials, but block the surface partially at lower potentials. A dual path reaction mechanism, common to all the alkaline solutions used, was proposed based on the assumptions that HCO is a reactive intermediate and that a formate is a reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media",
volume = "448",
number = "2",
pages = "173-181",
doi = "10.1016/S0022-0728(97)00141-1"
}
Tripković, A., Popović, K., Momčilović, J. D.,& Dražić, D. M.. (1998). Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media. in Journal of Electroanalytical Chemistry
Elsevier., 448(2), 173-181.
https://doi.org/10.1016/S0022-0728(97)00141-1
Tripković A, Popović K, Momčilović JD, Dražić DM. Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media. in Journal of Electroanalytical Chemistry. 1998;448(2):173-181.
doi:10.1016/S0022-0728(97)00141-1 .
Tripković, Amalija, Popović, Ksenija, Momčilović, J. D., Dražić, Dragutin M., "Kinetic and mechanistic study of methanol oxidation on a Pt 100/ surface in alkaline media" in Journal of Electroanalytical Chemistry, 448, no. 2 (1998):173-181,
https://doi.org/10.1016/S0022-0728(97)00141-1 . .
49
55
58

Oxygen reduction on a duplex stainless steel

Gojković, Snežana Lj.; Zečević, Strahinja K.; Obradović, Maja D.; Dražić, Dragutin M.

(Oxford : Pergamon-Elsevier Science Ltd, 1998)

TY  - JOUR
AU  - Gojković, Snežana Lj.
AU  - Zečević, Strahinja K.
AU  - Obradović, Maja D.
AU  - Dražić, Dragutin M.
PY  - 1998
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6342
AB  - O-2 reduction on duplex stainless steel was investigated in neutral and alkaline solutions with and without the presence of chloride ions. All polarization curves showed hysteresis with higher reaction rate in positive going sweep than in the negative one. Tafel slopes of about -90 mV dec(-1) in neutral and alkaline solutions without chloride ions and about -150 mV dec(-1) in NaCl solution were obtained. Reaction rate is almost independent on pH in solutions of pH lt 12 while in more alkaline solutions reaction order with respect to OH- ions of about -1 was obtained. Reaction rate and kinetic parameters for O-2 reduction on duplex stainless steel were compared to data for O-2 reduction on pure Fe and great similarity was found.
PB  - Oxford : Pergamon-Elsevier Science Ltd
T2  - Corrosion Science
T1  - Oxygen reduction on a duplex stainless steel
VL  - 40
IS  - 6
SP  - 849
EP  - 860
DO  - 10.1016/S0010-938X(98)00004-3
ER  - 
@article{
author = "Gojković, Snežana Lj. and Zečević, Strahinja K. and Obradović, Maja D. and Dražić, Dragutin M.",
year = "1998",
abstract = "O-2 reduction on duplex stainless steel was investigated in neutral and alkaline solutions with and without the presence of chloride ions. All polarization curves showed hysteresis with higher reaction rate in positive going sweep than in the negative one. Tafel slopes of about -90 mV dec(-1) in neutral and alkaline solutions without chloride ions and about -150 mV dec(-1) in NaCl solution were obtained. Reaction rate is almost independent on pH in solutions of pH lt 12 while in more alkaline solutions reaction order with respect to OH- ions of about -1 was obtained. Reaction rate and kinetic parameters for O-2 reduction on duplex stainless steel were compared to data for O-2 reduction on pure Fe and great similarity was found.",
publisher = "Oxford : Pergamon-Elsevier Science Ltd",
journal = "Corrosion Science",
title = "Oxygen reduction on a duplex stainless steel",
volume = "40",
number = "6",
pages = "849-860",
doi = "10.1016/S0010-938X(98)00004-3"
}
Gojković, S. Lj., Zečević, S. K., Obradović, M. D.,& Dražić, D. M.. (1998). Oxygen reduction on a duplex stainless steel. in Corrosion Science
Oxford : Pergamon-Elsevier Science Ltd., 40(6), 849-860.
https://doi.org/10.1016/S0010-938X(98)00004-3
Gojković SL, Zečević SK, Obradović MD, Dražić DM. Oxygen reduction on a duplex stainless steel. in Corrosion Science. 1998;40(6):849-860.
doi:10.1016/S0010-938X(98)00004-3 .
Gojković, Snežana Lj., Zečević, Strahinja K., Obradović, Maja D., Dražić, Dragutin M., "Oxygen reduction on a duplex stainless steel" in Corrosion Science, 40, no. 6 (1998):849-860,
https://doi.org/10.1016/S0010-938X(98)00004-3 . .
37
27
35

Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media

Tripković, Amalija; Popović, Ksenija; Momčilović, J. D.; Dražić, Dragutin M.

(Elsevier, 1998)

TY  - JOUR
AU  - Tripković, Amalija
AU  - Popović, Ksenija
AU  - Momčilović, J. D.
AU  - Dražić, Dragutin M.
PY  - 1998
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4144
AB  - The comparative study of methanol oxidation on a Pt(110) surface was carried out in bicarbonate, carbonate and sodium hydroxide solutions. It was shown that OH- electrosorption precedes the oxide layer formation in sodium hydroxide solution and is coupled by HCO3- and CO32- electrosorption in the corresponding media. Adsorbed bicarbonates suppressed the methanol oxidation. The surface activity was correlated to the OHad species coverage. Coverage with 'poisoning species' formed during methanol oxidation is time dependent. The dual path mechanism for methanol oxidation on the Pt(110) surface, as well as for the other low-index planes, was proposed based on the assumptions that HCOad and OHad are reactive intermediates and that formate is the reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media
VL  - 44
IS  - 6-7
SP  - 1135
EP  - 1145
DO  - 10.1016/S0013-4686(98)00216-3
ER  - 
@article{
author = "Tripković, Amalija and Popović, Ksenija and Momčilović, J. D. and Dražić, Dragutin M.",
year = "1998",
abstract = "The comparative study of methanol oxidation on a Pt(110) surface was carried out in bicarbonate, carbonate and sodium hydroxide solutions. It was shown that OH- electrosorption precedes the oxide layer formation in sodium hydroxide solution and is coupled by HCO3- and CO32- electrosorption in the corresponding media. Adsorbed bicarbonates suppressed the methanol oxidation. The surface activity was correlated to the OHad species coverage. Coverage with 'poisoning species' formed during methanol oxidation is time dependent. The dual path mechanism for methanol oxidation on the Pt(110) surface, as well as for the other low-index planes, was proposed based on the assumptions that HCOad and OHad are reactive intermediates and that formate is the reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media",
volume = "44",
number = "6-7",
pages = "1135-1145",
doi = "10.1016/S0013-4686(98)00216-3"
}
Tripković, A., Popović, K., Momčilović, J. D.,& Dražić, D. M.. (1998). Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media. in Electrochimica Acta
Elsevier., 44(6-7), 1135-1145.
https://doi.org/10.1016/S0013-4686(98)00216-3
Tripković A, Popović K, Momčilović JD, Dražić DM. Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media. in Electrochimica Acta. 1998;44(6-7):1135-1145.
doi:10.1016/S0013-4686(98)00216-3 .
Tripković, Amalija, Popović, Ksenija, Momčilović, J. D., Dražić, Dragutin M., "Kinetic and mechanistic study of methanol oxidation on a Pt(110) surface in alkaline media" in Electrochimica Acta, 44, no. 6-7 (1998):1135-1145,
https://doi.org/10.1016/S0013-4686(98)00216-3 . .
70
72
77

Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media

Tripković, Amalija; Popović, Ksenija; Momčilović, J. D.; Dražić, Dragutin M.

(Elsevier, 1996)

TY  - JOUR
AU  - Tripković, Amalija
AU  - Popović, Ksenija
AU  - Momčilović, J. D.
AU  - Dražić, Dragutin M.
PY  - 1996
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4199
AB  - A comparative study of methanol oxidation on a Pt(111) surface was carried out in bicarbonate, carbonate and different pH values of sodium hydroxide solutions. The surface activity was directly correlated to the OHad species coverage. It was shown that the 'poisoning species', produced in methanol oxidation, participate in the reaction although they partially block the surface, particularly at lower potentials. A dual path reaction mechanism, common to all alkaline solutions used, was proposed. It was based on the assumptions that HCO is a reactive intermediate and that formate is a reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media
VL  - 418
IS  - 1-2
SP  - 9
EP  - 20
DO  - 10.1016/S0022-0728(96)04849-8
ER  - 
@article{
author = "Tripković, Amalija and Popović, Ksenija and Momčilović, J. D. and Dražić, Dragutin M.",
year = "1996",
abstract = "A comparative study of methanol oxidation on a Pt(111) surface was carried out in bicarbonate, carbonate and different pH values of sodium hydroxide solutions. The surface activity was directly correlated to the OHad species coverage. It was shown that the 'poisoning species', produced in methanol oxidation, participate in the reaction although they partially block the surface, particularly at lower potentials. A dual path reaction mechanism, common to all alkaline solutions used, was proposed. It was based on the assumptions that HCO is a reactive intermediate and that formate is a reaction product in the main path, while CO2 is a product of 'poisoning species' oxidation in a parallel reaction path.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media",
volume = "418",
number = "1-2",
pages = "9-20",
doi = "10.1016/S0022-0728(96)04849-8"
}
Tripković, A., Popović, K., Momčilović, J. D.,& Dražić, D. M.. (1996). Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media. in Journal of Electroanalytical Chemistry
Elsevier., 418(1-2), 9-20.
https://doi.org/10.1016/S0022-0728(96)04849-8
Tripković A, Popović K, Momčilović JD, Dražić DM. Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media. in Journal of Electroanalytical Chemistry. 1996;418(1-2):9-20.
doi:10.1016/S0022-0728(96)04849-8 .
Tripković, Amalija, Popović, Ksenija, Momčilović, J. D., Dražić, Dragutin M., "Kinetic and mechanistic study of methanol oxidation on a Pt(111) surface in alkaline media" in Journal of Electroanalytical Chemistry, 418, no. 1-2 (1996):9-20,
https://doi.org/10.1016/S0022-0728(96)04849-8 . .
3
99
98
109

Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions

Zečević, Strahinja K.; Dražić, Dragutin M.; Gojković, Snežana Lj.

(Elsevier, 1991)

TY  - JOUR
AU  - Zečević, Strahinja K.
AU  - Dražić, Dragutin M.
AU  - Gojković, Snežana Lj.
PY  - 1991
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4316
AB  - The kinetics of hydrogen peroxide reduction were studied on iron in borate buffered and unbuffered solutions of pH ranging from 8.6 to 13.8, with and without the presence of chloride ions. A rotating disk electrode was employed. Measurements were taken using the linear sweep technique and the potential step steady-state technique. The H2O2 reduction on iron under these conditions was found to occur on the oxidized surfaces. The E-j polarization curves showed a significant hysteresis which is due to oxide film formation. On less oxidized and/or prereduced surfaces the H2O2 reduction was found to be faster than on more oxidized and/or prepassive surfaces. The reaction order with respect to H2O2 was found to be one. The rate determining step most likely involves the transfer of the first electron to the molecular H2O2. The ionic peroxide form HO-2 was not observed to be an electroactive species. The H2O2 reduction was found to be pH dependent at pH > 11. The observed pH dependence mostly reflects the acid-base equilibrium properties of H2O2 and partially those of the passive iron oxide film. Chloride ions were found not to have any influence on the reaction kinetics.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions
VL  - 36
IS  - 1
SP  - 5
EP  - 14
DO  - 10.1016/0013-4686(91)85172-4
ER  - 
@article{
author = "Zečević, Strahinja K. and Dražić, Dragutin M. and Gojković, Snežana Lj.",
year = "1991",
abstract = "The kinetics of hydrogen peroxide reduction were studied on iron in borate buffered and unbuffered solutions of pH ranging from 8.6 to 13.8, with and without the presence of chloride ions. A rotating disk electrode was employed. Measurements were taken using the linear sweep technique and the potential step steady-state technique. The H2O2 reduction on iron under these conditions was found to occur on the oxidized surfaces. The E-j polarization curves showed a significant hysteresis which is due to oxide film formation. On less oxidized and/or prereduced surfaces the H2O2 reduction was found to be faster than on more oxidized and/or prepassive surfaces. The reaction order with respect to H2O2 was found to be one. The rate determining step most likely involves the transfer of the first electron to the molecular H2O2. The ionic peroxide form HO-2 was not observed to be an electroactive species. The H2O2 reduction was found to be pH dependent at pH > 11. The observed pH dependence mostly reflects the acid-base equilibrium properties of H2O2 and partially those of the passive iron oxide film. Chloride ions were found not to have any influence on the reaction kinetics.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions",
volume = "36",
number = "1",
pages = "5-14",
doi = "10.1016/0013-4686(91)85172-4"
}
Zečević, S. K., Dražić, D. M.,& Gojković, S. Lj.. (1991). Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions. in Electrochimica Acta
Elsevier., 36(1), 5-14.
https://doi.org/10.1016/0013-4686(91)85172-4
Zečević SK, Dražić DM, Gojković SL. Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions. in Electrochimica Acta. 1991;36(1):5-14.
doi:10.1016/0013-4686(91)85172-4 .
Zečević, Strahinja K., Dražić, Dragutin M., Gojković, Snežana Lj., "Oxygen reduction on iron-IV. The reduction of hydrogen peroxide as the intermediate in oxygen reduction reaction in alkaline solutions" in Electrochimica Acta, 36, no. 1 (1991):5-14,
https://doi.org/10.1016/0013-4686(91)85172-4 . .
41
46

Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range

Zečević, Strahinja K.; Dražić, Dragutin M.; Gojković, S.

(Elsevier, 1991)

TY  - JOUR
AU  - Zečević, Strahinja K.
AU  - Dražić, Dragutin M.
AU  - Gojković, S.
PY  - 1991
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4378
AB  - O2 and H2O2 reduction was studied on Puratronic iron (99.995%) in borate buffer solutions of various pH ranging from 7.4 to 9.8. In solutions of pH < 9.3 the E-j curves are of quite irregular shapes and the limiting current is not established. Yet, in the potential region of the passivation-depassivation peak, a decrease in O2 and H2O2 reduction currents over time was observed. The influence of the passivation parameters (potential, time, speed, atmosphere and presence of H2O2 in the solution) on the degree of the inhibition of O2 and H2O2 reductions was examined. The loss of the electrocatalytic activity of the iron electrode is suggested to be due to the reaction between H2O2 and Fe(II) ions during the iron dissolution process occurring under the passivation-depassivation peak. The product of this reaction is an unconductive film which blocks the active electrode surface.
PB  - Elsevier
T2  - Corrosion Science
T1  - Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range
VL  - 32
IS  - 5-6
SP  - 563
EP  - 576
DO  - 10.1016/0010-938X(91)90107-Z
ER  - 
@article{
author = "Zečević, Strahinja K. and Dražić, Dragutin M. and Gojković, S.",
year = "1991",
abstract = "O2 and H2O2 reduction was studied on Puratronic iron (99.995%) in borate buffer solutions of various pH ranging from 7.4 to 9.8. In solutions of pH < 9.3 the E-j curves are of quite irregular shapes and the limiting current is not established. Yet, in the potential region of the passivation-depassivation peak, a decrease in O2 and H2O2 reduction currents over time was observed. The influence of the passivation parameters (potential, time, speed, atmosphere and presence of H2O2 in the solution) on the degree of the inhibition of O2 and H2O2 reductions was examined. The loss of the electrocatalytic activity of the iron electrode is suggested to be due to the reaction between H2O2 and Fe(II) ions during the iron dissolution process occurring under the passivation-depassivation peak. The product of this reaction is an unconductive film which blocks the active electrode surface.",
publisher = "Elsevier",
journal = "Corrosion Science",
title = "Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range",
volume = "32",
number = "5-6",
pages = "563-576",
doi = "10.1016/0010-938X(91)90107-Z"
}
Zečević, S. K., Dražić, D. M.,& Gojković, S.. (1991). Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range. in Corrosion Science
Elsevier., 32(5-6), 563-576.
https://doi.org/10.1016/0010-938X(91)90107-Z
Zečević SK, Dražić DM, Gojković S. Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range. in Corrosion Science. 1991;32(5-6):563-576.
doi:10.1016/0010-938X(91)90107-Z .
Zečević, Strahinja K., Dražić, Dragutin M., Gojković, S., "Oxygen reduction on iron-V. Processes in boric acid-borate buffer solutions in the 7.4-9.8 pH range" in Corrosion Science, 32, no. 5-6 (1991):563-576,
https://doi.org/10.1016/0010-938X(91)90107-Z . .
13
14

Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions

Zečević, Strahinja K.; Dražić, Dragutin M.; Gojković, Snežana Lj.

(Elsevier, 1989)

TY  - JOUR
AU  - Zečević, Strahinja K.
AU  - Dražić, Dragutin M.
AU  - Gojković, Snežana Lj.
PY  - 1989
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4209
AB  - The kinetics of oxygen reduction were studied on iron in borate and bicarbonate buffered solutions, pH 9.8, using the rotating disk-ring method. Under these conditions O2 reduction occurs both on the oxidized surface and on the oxide-free one, depending on potential. On the oxidized surface the series mechanism was found to be operative. On the oxide-free surface the four-electron reduction was observed, but, due to the very small rate of H2O2 formation with respect to the total reduction current, a reliable distinction between the parallel and series mechanism could not be made. All the rate constants of the O2 and H2O2 reactions on the Fe surface were determined. No catalytic decomposition of H2O2 was found. The kinetics of the O2 reduction reaction is slower on more oxidized surfaces.
PB  - Elsevier
T2  - Journal of Electroanalytical Chemistry
T1  - Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions
VL  - 265
IS  - 1-2
SP  - 179
EP  - 193
DO  - 10.1016/0022-0728(89)80188-3
ER  - 
@article{
author = "Zečević, Strahinja K. and Dražić, Dragutin M. and Gojković, Snežana Lj.",
year = "1989",
abstract = "The kinetics of oxygen reduction were studied on iron in borate and bicarbonate buffered solutions, pH 9.8, using the rotating disk-ring method. Under these conditions O2 reduction occurs both on the oxidized surface and on the oxide-free one, depending on potential. On the oxidized surface the series mechanism was found to be operative. On the oxide-free surface the four-electron reduction was observed, but, due to the very small rate of H2O2 formation with respect to the total reduction current, a reliable distinction between the parallel and series mechanism could not be made. All the rate constants of the O2 and H2O2 reactions on the Fe surface were determined. No catalytic decomposition of H2O2 was found. The kinetics of the O2 reduction reaction is slower on more oxidized surfaces.",
publisher = "Elsevier",
journal = "Journal of Electroanalytical Chemistry",
title = "Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions",
volume = "265",
number = "1-2",
pages = "179-193",
doi = "10.1016/0022-0728(89)80188-3"
}
Zečević, S. K., Dražić, D. M.,& Gojković, S. Lj.. (1989). Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions. in Journal of Electroanalytical Chemistry
Elsevier., 265(1-2), 179-193.
https://doi.org/10.1016/0022-0728(89)80188-3
Zečević SK, Dražić DM, Gojković SL. Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions. in Journal of Electroanalytical Chemistry. 1989;265(1-2):179-193.
doi:10.1016/0022-0728(89)80188-3 .
Zečević, Strahinja K., Dražić, Dragutin M., Gojković, Snežana Lj., "Oxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutions" in Journal of Electroanalytical Chemistry, 265, no. 1-2 (1989):179-193,
https://doi.org/10.1016/0022-0728(89)80188-3 . .
62
72

Activation of aluminium in chloride containing solutions

Stevanović, Rade M.; Despić, Aleksandar R.; Dražić, Dragutin M.

(Elsevier, 1988)

TY  - JOUR
AU  - Stevanović, Rade M.
AU  - Despić, Aleksandar R.
AU  - Dražić, Dragutin M.
PY  - 1988
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4313
AB  - Galvanostatic transients were recorded for anodic dissolution of high purity aluminium in neutral chloride solutions. All transients, except at very low current densities (below 50 μA cm-2), are characterized by an overshoot and a sudden decay of potential to the potential plateau of active anodic dissolution. Initial portions of the transients were analyzed for electrode capacitance and oxide growth. Sudden decay is interpreted in terms of adsorption of chloride and its effect on the structure and conductivity of the oxide film.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - Activation of aluminium in chloride containing solutions
VL  - 33
IS  - 3
SP  - 397
EP  - 404
DO  - 10.1016/0013-4686(88)85035-7
ER  - 
@article{
author = "Stevanović, Rade M. and Despić, Aleksandar R. and Dražić, Dragutin M.",
year = "1988",
abstract = "Galvanostatic transients were recorded for anodic dissolution of high purity aluminium in neutral chloride solutions. All transients, except at very low current densities (below 50 μA cm-2), are characterized by an overshoot and a sudden decay of potential to the potential plateau of active anodic dissolution. Initial portions of the transients were analyzed for electrode capacitance and oxide growth. Sudden decay is interpreted in terms of adsorption of chloride and its effect on the structure and conductivity of the oxide film.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "Activation of aluminium in chloride containing solutions",
volume = "33",
number = "3",
pages = "397-404",
doi = "10.1016/0013-4686(88)85035-7"
}
Stevanović, R. M., Despić, A. R.,& Dražić, D. M.. (1988). Activation of aluminium in chloride containing solutions. in Electrochimica Acta
Elsevier., 33(3), 397-404.
https://doi.org/10.1016/0013-4686(88)85035-7
Stevanović RM, Despić AR, Dražić DM. Activation of aluminium in chloride containing solutions. in Electrochimica Acta. 1988;33(3):397-404.
doi:10.1016/0013-4686(88)85035-7 .
Stevanović, Rade M., Despić, Aleksandar R., Dražić, Dragutin M., "Activation of aluminium in chloride containing solutions" in Electrochimica Acta, 33, no. 3 (1988):397-404,
https://doi.org/10.1016/0013-4686(88)85035-7 . .
36
45

Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions

Dražić, Dragutin M.; Chen, Shen Hao

(Elsevier, 1983)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Chen, Shen Hao
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4411
AB  - The possible inhibiting effects of GaO33-, GeO32-, CrO32-, and MoO42- ions on anodic and cathodic reactions on iron in 5 M KOH were studied. It was shown that a concentration of these ions of 10-3 M inhibits the anodic iron dissolution reaction 2-3 times, while no effect on the hydrogen evolution reaction was observed. The effect was explained by the underpotential deposition of adatoms of the metal complexing ions on the iron electrode.
PB  - Elsevier
T2  - Corrosion Science
T1  - Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions
VL  - 23
IS  - 7
SP  - 683
EP  - 686
DO  - 10.1016/0010-938X(83)90032-X
ER  - 
@article{
author = "Dražić, Dragutin M. and Chen, Shen Hao",
year = "1983",
abstract = "The possible inhibiting effects of GaO33-, GeO32-, CrO32-, and MoO42- ions on anodic and cathodic reactions on iron in 5 M KOH were studied. It was shown that a concentration of these ions of 10-3 M inhibits the anodic iron dissolution reaction 2-3 times, while no effect on the hydrogen evolution reaction was observed. The effect was explained by the underpotential deposition of adatoms of the metal complexing ions on the iron electrode.",
publisher = "Elsevier",
journal = "Corrosion Science",
title = "Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions",
volume = "23",
number = "7",
pages = "683-686",
doi = "10.1016/0010-938X(83)90032-X"
}
Dražić, D. M.,& Chen, S. H.. (1983). Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions. in Corrosion Science
Elsevier., 23(7), 683-686.
https://doi.org/10.1016/0010-938X(83)90032-X
Dražić DM, Chen SH. Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions. in Corrosion Science. 1983;23(7):683-686.
doi:10.1016/0010-938X(83)90032-X .
Dražić, Dragutin M., Chen, Shen Hao, "Inhibition of the anodic dissolution of iron in alkaline solution by metal complex ions" in Corrosion Science, 23, no. 7 (1983):683-686,
https://doi.org/10.1016/0010-938X(83)90032-X . .
8
6

The effect of anions on the electrochemical behaviour of aluminium

Dražić, Dragutin M.; Zečević, Strahinja K.; Atanasoski, Radoslav; Despić, Aleksandar

(Elsevier, 1983)

TY  - JOUR
AU  - Dražić, Dragutin M.
AU  - Zečević, Strahinja K.
AU  - Atanasoski, Radoslav
AU  - Despić, Aleksandar
PY  - 1983
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4415
AB  - Aluminum has been known to exhibit widely different electrochemical properties in different aqueous electrolytes. Thus, OH- ions in strongly alkaline solutions reveal its strong affinity to water by dissolving its protective oxide film. The metal establishes a very negative electrode potential, undergoing violent corrosion resulting in the evolution of hydrogen and the formation of aluminate ions. In this communication, some experiments on the effect of activity promoting anions are presented and a model is forwarded for a possible explanation of the observed phenomena.
PB  - Elsevier
T2  - Electrochimica Acta
T1  - The effect of anions on the electrochemical behaviour of aluminium
VL  - 28
IS  - 5
SP  - 751
EP  - 755
DO  - 10.1016/0013-4686(83)85076-2
ER  - 
@article{
author = "Dražić, Dragutin M. and Zečević, Strahinja K. and Atanasoski, Radoslav and Despić, Aleksandar",
year = "1983",
abstract = "Aluminum has been known to exhibit widely different electrochemical properties in different aqueous electrolytes. Thus, OH- ions in strongly alkaline solutions reveal its strong affinity to water by dissolving its protective oxide film. The metal establishes a very negative electrode potential, undergoing violent corrosion resulting in the evolution of hydrogen and the formation of aluminate ions. In this communication, some experiments on the effect of activity promoting anions are presented and a model is forwarded for a possible explanation of the observed phenomena.",
publisher = "Elsevier",
journal = "Electrochimica Acta",
title = "The effect of anions on the electrochemical behaviour of aluminium",
volume = "28",
number = "5",
pages = "751-755",
doi = "10.1016/0013-4686(83)85076-2"
}
Dražić, D. M., Zečević, S. K., Atanasoski, R.,& Despić, A.. (1983). The effect of anions on the electrochemical behaviour of aluminium. in Electrochimica Acta
Elsevier., 28(5), 751-755.
https://doi.org/10.1016/0013-4686(83)85076-2
Dražić DM, Zečević SK, Atanasoski R, Despić A. The effect of anions on the electrochemical behaviour of aluminium. in Electrochimica Acta. 1983;28(5):751-755.
doi:10.1016/0013-4686(83)85076-2 .
Dražić, Dragutin M., Zečević, Strahinja K., Atanasoski, Radoslav, Despić, Aleksandar, "The effect of anions on the electrochemical behaviour of aluminium" in Electrochimica Acta, 28, no. 5 (1983):751-755,
https://doi.org/10.1016/0013-4686(83)85076-2 . .
74
94