Synthesis of binary Co–Mg–O oxide system and study of its behavior in reduction/oxidation cycling; International Journal of Hydrogen Energy; Vol. 44, iss. 37

Bibliografski detalji
Parent link:International Journal of Hydrogen Energy
Vol. 44, iss. 37.— 2019.— [P. 20690-20699]
Autor kompanije: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий
Daljnji autori: Vedyagin A. A. Aleksey Anatolievich, Karnaukhov T. M. Timofey, Cherepanova S. V. Svetlana, Stoyanovskii V. O. Vladimir, Rogov V. A. Vladimir, Mishakov I. V.
Sažetak:Title screen
The nanoscale Co-Mg-O oxide sample (15 wt% in terms of Co3O4) was prepared from the corresponding xerogel synthesized by the modified sol-gel method. The hydrolysis of as-prepared Mg(OCH3)2 was carried out using the aqueous solution of Co(NO3)2 precursor. The CoOx nanocrystallites of about 10-20 nm in size were shown to be uniformly distributed within the MgO matrix. The reduction of Co-Mg-O in H2 flow was found to proceed in two separate stages within the temperature ranges of 200-350 °C and 350-600 °C. The prepared binary Co-Mg-O system was demonstrated to possess completely reproducible reduction behavior in the consecutive reduction/reoxidation cycles. The phase composition of the sample exposed to both the reducing and oxidative environment was followed by an in situ X-ray diffraction analysis performed at temperatures of 25, 300, 500 and 700 °C. The determined lattice parameters for MgO (a = 4.219 Å) and Co3O4 (a = 8.110 Å) were found to be slightly increased as compared with the values from Powder Diffraction File, so that the formation of joint non-stoichiometric (Mg1-xCox)O and (Co3-xMgx)O4 phases was suggested. The strong chemical interaction of cobalt oxide with MgO matrix was also evidenced by the data of a diffuse reflectance UV-vis spectroscopy.
Режим доступа: по договору с организацией-держателем ресурса
Jezik:engleski
Izdano: 2019
Teme:
Online pristup:https://doi.org/10.1016/j.ijhydene.2018.05.044
Format: Elektronički Poglavlje knjige
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=661245

MARC

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300 |a Title screen 
320 |a [References: 49 tit.] 
330 |a The nanoscale Co-Mg-O oxide sample (15 wt% in terms of Co3O4) was prepared from the corresponding xerogel synthesized by the modified sol-gel method. The hydrolysis of as-prepared Mg(OCH3)2 was carried out using the aqueous solution of Co(NO3)2 precursor. The CoOx nanocrystallites of about 10-20 nm in size were shown to be uniformly distributed within the MgO matrix. The reduction of Co-Mg-O in H2 flow was found to proceed in two separate stages within the temperature ranges of 200-350 °C and 350-600 °C. The prepared binary Co-Mg-O system was demonstrated to possess completely reproducible reduction behavior in the consecutive reduction/reoxidation cycles. The phase composition of the sample exposed to both the reducing and oxidative environment was followed by an in situ X-ray diffraction analysis performed at temperatures of 25, 300, 500 and 700 °C. The determined lattice parameters for MgO (a = 4.219 Å) and Co3O4 (a = 8.110 Å) were found to be slightly increased as compared with the values from Powder Diffraction File, so that the formation of joint non-stoichiometric (Mg1-xCox)O and (Co3-xMgx)O4 phases was suggested. The strong chemical interaction of cobalt oxide with MgO matrix was also evidenced by the data of a diffuse reflectance UV-vis spectroscopy. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t International Journal of Hydrogen Energy 
463 |t Vol. 44, iss. 37  |v [P. 20690-20699]  |d 2019 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a sol-gel technique 
610 1 |a nanocrystalline MgO 
610 1 |a cobalt oxide 
610 1 |a solid solutions 
610 1 |a reduction behavior 
610 1 |a золь-гель технологии 
610 1 |a оксид кобальта 
610 1 |a твердые растворы 
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701 1 |a Karnaukhov  |b T. M.  |g Timofey 
701 1 |a Cherepanova  |b S. V.  |g Svetlana 
701 1 |a Stoyanovskii  |b V. O.  |g Vladimir 
701 1 |a Rogov  |b V. A.  |g Vladimir 
701 1 |a Mishakov  |b I. V. 
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