Hydrogen evolution at Zn-Ni alloys
Samo za registrovane korisnike
1998
Članak u časopisu (Objavljena verzija)
Metapodaci
Prikaz svih podataka o dokumentuApstrakt
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.
Ključne reči:
Ni-Zn alloy / alloy electrodeposition / phase structure / herIzvor:
Electrochimica Acta, 1998, 43, 7, 705-711Izdavač:
- Pergamon-Elsevier Science Ltd, Oxford
DOI: 10.1016/S0013-4686(97)00142-4
ISSN: 0013-4686
WoS: 000071490500009
Scopus: 2-s2.0-0032316842
Institucija/grupa
Tehnološko-metalurški fakultetTY - JOUR AU - Stevanović, Jasmina AU - Gojković, Snežana Lj. AU - Despić, A AU - Obradović, M AU - Nakić, V PY - 1998 UR - http://TechnoRep.tmf.bg.ac.rs/handle/123456789/219 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 EP - 711 IS - 7 SP - 705 VL - 43 DO - 10.1016/S0013-4686(97)00142-4 ER -
@article{ author = "Stevanović, Jasmina and Gojković, Snežana Lj. and Despić, A and Obradović, M and Nakić, V", 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", pages = "711-705", number = "7", volume = "43", doi = "10.1016/S0013-4686(97)00142-4" }
Stevanović, J., Gojković, S. Lj., Despić, A., Obradović, M.,& Nakić, V.. (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 SL, Despić A, Obradović M, Nakić V. 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 Lj., Despić, A, Obradović, M, Nakić, V, "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 . .