Direct Synthesis of Sulphide Multifunctional Catalysts for Hydrogenolysis; Molecular Aspects of Catalysis by Sulfides (MACS)

Бібліографічні деталі
Parent link:Molecular Aspects of Catalysis by Sulfides (MACS).— 2013.— [1 p.]
Співавтор: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра химической технологии топлива и химической кибернетики (ХТТ)
Інші автори: Fedushchak T. A. Taisiya Alexandrovna, Akimov A. S. Akim Semenovich, Morozov M. A. Maxim Alexandrovich, Vosmerikov A. V., Uimin M. A. Mikhail Alexandrovich, Zhuravkov S. P. Sergey Petrovich
Резюме:New technologies for production of bulk catalysts require that the available catalyst systems be essentially improved. The advantage of bulk catalysts on inflicted catalysts is in the freedom to vary the active component concentration in a wide range of values. Bulk sulfide catalysts are usually prepared by co-precipitation, mechanical activation of precursor salts and micelar synthesis of solid sulfide particles. Furthermore Мо/W and 3d-metal oxides are always formed as intermediates. According to the literature attempts to obtain highly active catalyst for hydrogenolysis from macrocrystalline MoS2 failed to be success. In this paper we present the results on direct solid-phase synthesis of sulfide catalysts based on different MoS2 (MoS2, obtained by self-propagating high-temperature synthesis from electroexplosive Мо nano-powder and elemental S, Fig.1а, and commercial macrocrystalline product, Fig.1b), as well promoters taken as electro-explosive nano-sized Ni and Со powders or micron-sized powders. Nano-fiber γ-AlOOH (Fig.1d), obtained from electro-explosive nano-powder AlN and detonation nano-diamonds were used as binders. Solid-phase synthesis of the catalytic systems was carried out via mechanical activation of MoS2 and promoters at dispersion during 4 - 24 hours.
Мова:Англійська
Опубліковано: 2013
Предмети:
Онлайн доступ:https://www.elibrary.ru/item.asp?id=50301429
Формат: Електронний ресурс Частина з книги
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=669225

MARC

LEADER 00000naa0a2200000 4500
001 669225
005 20250707131906.0
035 |a (RuTPU)RU\TPU\network\40465 
035 |a RU\TPU\network\40464 
090 |a 669225 
100 |a 20230302d2013 k||y0rusy50 ba 
101 0 |a eng 
102 |a NL 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Direct Synthesis of Sulphide Multifunctional Catalysts for Hydrogenolysis  |f T. A. Fedushchak, A. S. Akimov, M. A. Morozov [et al.] 
203 |a Текст  |c электронный 
320 |a [References: 2 tit.] 
330 |a New technologies for production of bulk catalysts require that the available catalyst systems be essentially improved. The advantage of bulk catalysts on inflicted catalysts is in the freedom to vary the active component concentration in a wide range of values. Bulk sulfide catalysts are usually prepared by co-precipitation, mechanical activation of precursor salts and micelar synthesis of solid sulfide particles. Furthermore Мо/W and 3d-metal oxides are always formed as intermediates. According to the literature attempts to obtain highly active catalyst for hydrogenolysis from macrocrystalline MoS2 failed to be success. In this paper we present the results on direct solid-phase synthesis of sulfide catalysts based on different MoS2 (MoS2, obtained by self-propagating high-temperature synthesis from electroexplosive Мо nano-powder and elemental S, Fig.1а, and commercial macrocrystalline product, Fig.1b), as well promoters taken as electro-explosive nano-sized Ni and Со powders or micron-sized powders. Nano-fiber γ-AlOOH (Fig.1d), obtained from electro-explosive nano-powder AlN and detonation nano-diamonds were used as binders. Solid-phase synthesis of the catalytic systems was carried out via mechanical activation of MoS2 and promoters at dispersion during 4 - 24 hours. 
463 |t Molecular Aspects of Catalysis by Sulfides (MACS)  |o VIth International Symposium, 12-16 May, 2013 Satillieu, France  |v [1 p.]  |d 2013 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
701 1 |a Fedushchak  |b T. A.  |g Taisiya Alexandrovna 
701 1 |a Akimov  |b A. S.  |g Akim Semenovich 
701 1 |a Morozov  |b M. A.  |g Maxim Alexandrovich 
701 1 |a Vosmerikov  |b A. V. 
701 1 |a Uimin  |b M. A.  |g Mikhail Alexandrovich 
701 1 |a Zhuravkov  |b S. P.  |c chemist  |c Leading Researcher, Associate Professor of Tomsk Polytechnic University, Candidate of Chemical Sciences  |f 1961-  |g Sergey Petrovich  |3 (RuTPU)RU\TPU\pers\31297  |9 15475 
712 0 2 |a Национальный исследовательский Томский политехнический университет (ТПУ)  |b Институт природных ресурсов (ИПР)  |b Кафедра химической технологии топлива и химической кибернетики (ХТТ)  |3 (RuTPU)RU\TPU\col\18665 
801 2 |a RU  |b 63413507  |c 20230302  |g RCR 
850 |a 63413507 
856 4 |u https://www.elibrary.ru/item.asp?id=50301429  |z https://www.elibrary.ru/item.asp?id=50301429 
942 |c CF