Comparative study of 1,2-dichlorethane decomposition over Ni-based catalysts with formation of filamentous carbon

Bibliografiska uppgifter
Parent link:Catalysis Today
Vol. 301.— 2018.— [P. 147-152]
Institutionella upphovsmän: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий, Национальный исследовательский Томский политехнический университет Инженерная школа энергетики Научно-образовательный центр И. Н. Бутакова (НОЦ И. Н. Бутакова)
Övriga upphovsmän: Vedyagin A. A. Aleksey Anatolievich, Volodin A. M. Aleksandr, Kenzhin R. M. Roman, Stoyanovskii V. O. Vladimir, Rogov V. A. Vladimir, Kriventsov V. V. Vladimir Vladimirovich, Bauman Yu. I. Yury, Mishakov I. V. Iljya Vladimirovich, Korneev D. V. Denis, Shubin Yu. V. Yury Viktorovich, Buyanov R. A. Roman
Sammanfattning:Title screen
Catalytic chemical vapor deposition of 1,2-dichlorethane over Ni-based catalysts into carbon nanostructured materials was studied. The catalysts were prepared by mechanochemical activation and by metal dusting of bulk nickel-containing alloy precursors. Model Ni-M alloys, where M is Co, Cu, and Fe, were obtained by coprecipitation technique. Loading of M in the samples was varied in a range of 1–5 at.%. Pure nickel was used a reference. The kinetics of carbon deposition was investigated using flow reactor equipped with McBain balances. The samples of carbon product were characterized by nitrogen adsorption, scanning and transmission electron microscopies. The hydrogen addition into reaction mixture was shown to have opposite effect on both catalytic behavior and carbon yield depending on catalyst’s nature. Segmented structure of carbon filaments formed specifies its developed surface area. Both bulk chlorination of nickel particles and its blockage by dense carbon deposits in the case of mechanochemically prepared samples were suggested to be responsible for rapid deactivation of the catalyst.
Режим доступа: по договору с организацией-держателем ресурса
Publicerad: 2018
Ämnen:
Länkar:https://doi.org/10.1016/j.cattod.2017.05.015
Materialtyp: Elektronisk Bokavsnitt
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=666733