Standard

CO2 Methanation: Solvent-Free Synthesis of Nickel-Containing Catalysts from Complexes with Ethylenediamine. / Netskina, Olga V; Dmitruk, Kirill A; Mazina, Olga I и др.

в: Materials, Том 16, № 7, 2616, 25.03.2023.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

APA

Vancouver

Netskina OV, Dmitruk KA, Mazina OI, Paletsky AA, Mukha SA, Prosvirin IP и др. CO2 Methanation: Solvent-Free Synthesis of Nickel-Containing Catalysts from Complexes with Ethylenediamine. Materials. 2023 март 25;16(7):2616. doi: 10.3390/ma16072616

Author

BibTeX

@article{3f46607d67214a47b5a2177ecb026296,
title = "CO2 Methanation: Solvent-Free Synthesis of Nickel-Containing Catalysts from Complexes with Ethylenediamine",
abstract = "CO2 methanation was studied in the presence of nickel catalysts obtained by the solid-state combustion method. Complexes with a varying number of ethylenediamine molecules in the coordination sphere of nickel were chosen as the precursors of the active component of the catalysts. Their synthesis was carried out without the use of solvents, which made it possible to avoid the stages of their separation from the solution and the utilization of waste liquids. The composition and structure of the synthesized complexes were confirmed by elemental analysis, IR spectroscopy, powder XRD and XPS methods. It was determined that their thermal decomposition in the combustion wave proceeds in multiple stages with the formation of NiO and Ni(OH)2, which are reduced to Ni0. Higher ethylenediamine content in the complex leads to a higher content of metal in the solid products of combustion. However, different ratios of oxidized and reduced forms of nickel do not affect the initial activation temperature of nickel catalysts in the presence of CO2. It was noted that, after activation, the sample obtained from [Ni(C2H8N2)2](NO3)2 exhibited the highest activity in CO2 methanation. Thus, this complex is a promising precursor for CO2 methanation catalysts, and its synthesis requires only a small amount of ethylenediamine.",
author = "Netskina, {Olga V} and Dmitruk, {Kirill A} and Mazina, {Olga I} and Paletsky, {Alexander A} and Mukha, {Svetlana A} and Prosvirin, {Igor P} and Pochtar, {Alena A} and Bulavchenko, {Olga A} and Shmakov, {Andrey G} and Veselovskaya, {Janna V} and Komova, {Oxana V}",
note = "Funding: This work was supported by the Ministry of Science and Higher Education of the Russian Federation within the governmental order for the Boreskov Institute of Catalysis, project AAAA-A21-121011390006-0.",
year = "2023",
month = mar,
day = "25",
doi = "10.3390/ma16072616",
language = "English",
volume = "16",
journal = "Materials",
issn = "1996-1944",
publisher = "MDPI AG",
number = "7",

}

RIS

TY - JOUR

T1 - CO2 Methanation: Solvent-Free Synthesis of Nickel-Containing Catalysts from Complexes with Ethylenediamine

AU - Netskina, Olga V

AU - Dmitruk, Kirill A

AU - Mazina, Olga I

AU - Paletsky, Alexander A

AU - Mukha, Svetlana A

AU - Prosvirin, Igor P

AU - Pochtar, Alena A

AU - Bulavchenko, Olga A

AU - Shmakov, Andrey G

AU - Veselovskaya, Janna V

AU - Komova, Oxana V

N1 - Funding: This work was supported by the Ministry of Science and Higher Education of the Russian Federation within the governmental order for the Boreskov Institute of Catalysis, project AAAA-A21-121011390006-0.

PY - 2023/3/25

Y1 - 2023/3/25

N2 - CO2 methanation was studied in the presence of nickel catalysts obtained by the solid-state combustion method. Complexes with a varying number of ethylenediamine molecules in the coordination sphere of nickel were chosen as the precursors of the active component of the catalysts. Their synthesis was carried out without the use of solvents, which made it possible to avoid the stages of their separation from the solution and the utilization of waste liquids. The composition and structure of the synthesized complexes were confirmed by elemental analysis, IR spectroscopy, powder XRD and XPS methods. It was determined that their thermal decomposition in the combustion wave proceeds in multiple stages with the formation of NiO and Ni(OH)2, which are reduced to Ni0. Higher ethylenediamine content in the complex leads to a higher content of metal in the solid products of combustion. However, different ratios of oxidized and reduced forms of nickel do not affect the initial activation temperature of nickel catalysts in the presence of CO2. It was noted that, after activation, the sample obtained from [Ni(C2H8N2)2](NO3)2 exhibited the highest activity in CO2 methanation. Thus, this complex is a promising precursor for CO2 methanation catalysts, and its synthesis requires only a small amount of ethylenediamine.

AB - CO2 methanation was studied in the presence of nickel catalysts obtained by the solid-state combustion method. Complexes with a varying number of ethylenediamine molecules in the coordination sphere of nickel were chosen as the precursors of the active component of the catalysts. Their synthesis was carried out without the use of solvents, which made it possible to avoid the stages of their separation from the solution and the utilization of waste liquids. The composition and structure of the synthesized complexes were confirmed by elemental analysis, IR spectroscopy, powder XRD and XPS methods. It was determined that their thermal decomposition in the combustion wave proceeds in multiple stages with the formation of NiO and Ni(OH)2, which are reduced to Ni0. Higher ethylenediamine content in the complex leads to a higher content of metal in the solid products of combustion. However, different ratios of oxidized and reduced forms of nickel do not affect the initial activation temperature of nickel catalysts in the presence of CO2. It was noted that, after activation, the sample obtained from [Ni(C2H8N2)2](NO3)2 exhibited the highest activity in CO2 methanation. Thus, this complex is a promising precursor for CO2 methanation catalysts, and its synthesis requires only a small amount of ethylenediamine.

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85152548403&origin=inward&txGid=5881c5c7e92a8b90ef3c25f2c3219881

U2 - 10.3390/ma16072616

DO - 10.3390/ma16072616

M3 - Article

C2 - 37048912

VL - 16

JO - Materials

JF - Materials

SN - 1996-1944

IS - 7

M1 - 2616

ER -

ID: 47674548