TY  - JOUR
AU  - Stevanović, Jasmina
AU  - Gojković, Snežana
AU  - Despić, A.R.
AU  - Obradović, Maja D.
AU  - Nakić, Vjekoslav M.
PY  - 1998
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/6344
AB  - Zn-Ni alloys were electrodeposited from a berate-citrate and TEPA bath in potentiostatic and galvanostatic regimes. Potential of electrodeposition or current density were varied and chemical composition and phase structure were determined. It was found that both chemical composition and phase structure of alloys electrodeposited at the same potential or current density but in the two electrolytes were different. Differences were found even when one and the same chemical composition was achieved. Hydrogen evolution kinetics at the Zn-Ni alloys deposited from the two baths was investigated in alkaline solution (1 M NaOH). Substantial differences in the reaction rates at the alloys with the same chemical but different phase composition were found.
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Electrochimica Acta
T1  - Hydrogen evolution at Zn-Ni alloys
VL  - 43
IS  - 7
SP  - 705
EP  - 711
DO  - 10.1016/S0013-4686(97)00142-4
ER  - 

@article{
author = "Stevanović, Jasmina and Gojković, Snežana and Despić, A.R. and Obradović, Maja D. and Nakić, Vjekoslav M.",
year = "1998",
abstract = "Zn-Ni alloys were electrodeposited from a berate-citrate and TEPA bath in potentiostatic and galvanostatic regimes. Potential of electrodeposition or current density were varied and chemical composition and phase structure were determined. It was found that both chemical composition and phase structure of alloys electrodeposited at the same potential or current density but in the two electrolytes were different. Differences were found even when one and the same chemical composition was achieved. Hydrogen evolution kinetics at the Zn-Ni alloys deposited from the two baths was investigated in alkaline solution (1 M NaOH). Substantial differences in the reaction rates at the alloys with the same chemical but different phase composition were found.",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Electrochimica Acta",
title = "Hydrogen evolution at Zn-Ni alloys",
volume = "43",
number = "7",
pages = "705-711",
doi = "10.1016/S0013-4686(97)00142-4"
}

Stevanović, J., Gojković, S., Despić, A.R., Obradović, M. D.,& Nakić, V. M.. (1998). Hydrogen evolution at Zn-Ni alloys. in Electrochimica Acta
Pergamon-Elsevier Science Ltd, Oxford., 43(7), 705-711.
https://doi.org/10.1016/S0013-4686(97)00142-4

Stevanović J, Gojković S, Despić A, Obradović MD, Nakić VM. Hydrogen evolution at Zn-Ni alloys. in Electrochimica Acta. 1998;43(7):705-711.
doi:10.1016/S0013-4686(97)00142-4 .

Stevanović, Jasmina, Gojković, Snežana, Despić, A.R., Obradović, Maja D., Nakić, Vjekoslav M., "Hydrogen evolution at Zn-Ni alloys" in Electrochimica Acta, 43, no. 7 (1998):705-711,
https://doi.org/10.1016/S0013-4686(97)00142-4 . .

TY  - JOUR
AU  - Savić Maglić, G.
AU  - Despić, A.R.
PY  - 1973
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4717
AB  - A very low impedance circuit was constructed in order to provide a pulsating cathodic potential for a copper electrode immersed in a copper sulphate solution of the type used in copper refining. The increase in surface roughness during a fixed period of plating was investigated as a function of the frequency of pulsation. It was established that the relative increase in surface roughness depended linearly on the square root of the reciprocal frequency. This is in accordance with the theory based on the model of amplification of surface roughness being a transport controlled phenomenon.
PB  - Elsevier
T2  - Electrodeposition and Surface Treatments
T1  - Pulsating potential electrolysis in the deposition of copper
VL  - 1
IS  - 6
SP  - 429
EP  - 438
DO  - 10.1016/0300-9416(73)90026-6
ER  - 

@article{
author = "Savić Maglić, G. and Despić, A.R.",
year = "1973",
abstract = "A very low impedance circuit was constructed in order to provide a pulsating cathodic potential for a copper electrode immersed in a copper sulphate solution of the type used in copper refining. The increase in surface roughness during a fixed period of plating was investigated as a function of the frequency of pulsation. It was established that the relative increase in surface roughness depended linearly on the square root of the reciprocal frequency. This is in accordance with the theory based on the model of amplification of surface roughness being a transport controlled phenomenon.",
publisher = "Elsevier",
journal = "Electrodeposition and Surface Treatments",
title = "Pulsating potential electrolysis in the deposition of copper",
volume = "1",
number = "6",
pages = "429-438",
doi = "10.1016/0300-9416(73)90026-6"
}

Savić Maglić, G.,& Despić, A.R.. (1973). Pulsating potential electrolysis in the deposition of copper. in Electrodeposition and Surface Treatments
Elsevier., 1(6), 429-438.
https://doi.org/10.1016/0300-9416(73)90026-6

Savić Maglić G, Despić A. Pulsating potential electrolysis in the deposition of copper. in Electrodeposition and Surface Treatments. 1973;1(6):429-438.
doi:10.1016/0300-9416(73)90026-6 .

Savić Maglić, G., Despić, A.R., "Pulsating potential electrolysis in the deposition of copper" in Electrodeposition and Surface Treatments, 1, no. 6 (1973):429-438,
https://doi.org/10.1016/0300-9416(73)90026-6 . .

TY  - JOUR
AU  - Jakšić, M.M.
AU  - Despić, A.R.
AU  - Csonka, I.M.
AU  - Nikolić, B.Z.
PY  - 1969
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4653
AB  - A modified technology for electrolytic chlorate production has been developed.
The cell is considered as a hypochlorite generator and the holding
volume as a reactor for the conversion of available chlorine to chlorate. The
holding volume is operated at an elevated temperature.
The process as a whole then leads to higher current efficiencies. For such a closed-loop system,
theoretical relationships were established between the current efficiency and
other determining factors. These relationships were confirmed experimentally.
Foerster's theory of electrolytic chlorate formation has also been confirmed
by the present results.
PB  - IOP Publishing
T2  - Journal of Electrochemical Society
T1  - Studies on Chlorate Cell Process: V . Theory and Practice of a Modified Technology for Electrolytic Chlorate Production
VL  - 116
IS  - 9
SP  - 1316
EP  - 1322
DO  - 10.1149/1.2412309
ER  - 

@article{
author = "Jakšić, M.M. and Despić, A.R. and Csonka, I.M. and Nikolić, B.Z.",
year = "1969",
abstract = "A modified technology for electrolytic chlorate production has been developed.
The cell is considered as a hypochlorite generator and the holding
volume as a reactor for the conversion of available chlorine to chlorate. The
holding volume is operated at an elevated temperature.
The process as a whole then leads to higher current efficiencies. For such a closed-loop system,
theoretical relationships were established between the current efficiency and
other determining factors. These relationships were confirmed experimentally.
Foerster's theory of electrolytic chlorate formation has also been confirmed
by the present results.",
publisher = "IOP Publishing",
journal = "Journal of Electrochemical Society",
title = "Studies on Chlorate Cell Process: V . Theory and Practice of a Modified Technology for Electrolytic Chlorate Production",
volume = "116",
number = "9",
pages = "1316-1322",
doi = "10.1149/1.2412309"
}

Jakšić, M.M., Despić, A.R., Csonka, I.M.,& Nikolić, B.Z.. (1969). Studies on Chlorate Cell Process: V . Theory and Practice of a Modified Technology for Electrolytic Chlorate Production. in Journal of Electrochemical Society
IOP Publishing., 116(9), 1316-1322.
https://doi.org/10.1149/1.2412309

Jakšić M, Despić A, Csonka I, Nikolić B. Studies on Chlorate Cell Process: V . Theory and Practice of a Modified Technology for Electrolytic Chlorate Production. in Journal of Electrochemical Society. 1969;116(9):1316-1322.
doi:10.1149/1.2412309 .

Jakšić, M.M., Despić, A.R., Csonka, I.M., Nikolić, B.Z., "Studies on Chlorate Cell Process: V . Theory and Practice of a Modified Technology for Electrolytic Chlorate Production" in Journal of Electrochemical Society, 116, no. 9 (1969):1316-1322,
https://doi.org/10.1149/1.2412309 . .