Influence of Components Deposition Order on Silver Species Formation in Bimetallic Ag-Fe System Supported on Mordenite; Catalysts; Vol. 12 iss. 11

Dades bibliogràfiques
Parent link:Catalysts
Vol. 12 iss. 11.— 2022.— [1453, 20 p.]
Autor corporatiu: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий Лаборатория "Химическая инженерия и молекулярный дизайн"
Altres autors: Sanchez-Lopez P. Perla, Kotolevich Yu. Yulia, Antunez-Garcia J. Joel, Chavez-Rivas F. Fernando, Khramov E. Evgeny, Berlier G., Moreno-Ruiz L. Luis, Zubavichus Ya. Yan, Petranovskii V. Vitalii, Fuentes-Moyado S. Sergio, Pestryakov A. N. Aleksey Nikolaevich
Sumari:Title screen
In the present work, various experimental and theoretical methods were combined to study in detail the modifying effect of differences in the order of deposition of components on the state of silver in bimetallic iron-silver samples based on mordenite. In each of the silver-containing samples, the formation of large (≥2 nm in diameter) varieties of silver was observed, which differed from the varieties in the other samples, and in varying degrees. The formation of large Ag NPs on the outer surface of mordenite is explained by the redox interaction of Ag+-Fe2+ and the selectivity of ion exchange. The local surrounding of Ag in the studied samples is different: for AgMOR-monatomic species dominate, FeAgMOR-silver dimers and AgFeMOR-metal particles. In all investigated samples, the partially charged intra-channel Agnδ+ clusters (~0.7 nm in size) were formed due to partial Ag+ reduction and subsequent Ag0 agglomeration into the mordenite channel. Most of the silver in the bulk of the zeolite is represented in the cationic state attached to the mordenite framework by differently coordinated electrostatic forces, which can be Ag-O, Ag-Si or Ag-Al, with variations in interatomic distances and do not depend on the order of metal deposition. In addition, the arrangement of the cations in the side pockets means that the transport channels of mordenite are free, which is favorable for the application of the materials under study in catalysis and adsorption.
Idioma:anglès
Publicat: 2022
Matèries:
Accés en línia:https://doi.org/10.3390/catal12111453
Format: MixedMaterials Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=668878

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200 1 |a Influence of Components Deposition Order on Silver Species Formation in Bimetallic Ag-Fe System Supported on Mordenite  |f P. Sanchez-Lopez, Yu. Kotolevich, J. Antunez-Garcia [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 58 tit.] 
330 |a In the present work, various experimental and theoretical methods were combined to study in detail the modifying effect of differences in the order of deposition of components on the state of silver in bimetallic iron-silver samples based on mordenite. In each of the silver-containing samples, the formation of large (≥2 nm in diameter) varieties of silver was observed, which differed from the varieties in the other samples, and in varying degrees. The formation of large Ag NPs on the outer surface of mordenite is explained by the redox interaction of Ag+-Fe2+ and the selectivity of ion exchange. The local surrounding of Ag in the studied samples is different: for AgMOR-monatomic species dominate, FeAgMOR-silver dimers and AgFeMOR-metal particles. In all investigated samples, the partially charged intra-channel Agnδ+ clusters (~0.7 nm in size) were formed due to partial Ag+ reduction and subsequent Ag0 agglomeration into the mordenite channel. Most of the silver in the bulk of the zeolite is represented in the cationic state attached to the mordenite framework by differently coordinated electrostatic forces, which can be Ag-O, Ag-Si or Ag-Al, with variations in interatomic distances and do not depend on the order of metal deposition. In addition, the arrangement of the cations in the side pockets means that the transport channels of mordenite are free, which is favorable for the application of the materials under study in catalysis and adsorption. 
461 |t Catalysts 
463 |t Vol. 12 iss. 11  |v [1453, 20 p.]  |d 2022 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a mordenite 
610 1 |a silver species 
610 1 |a ion exchange 
610 1 |a deposition order 
610 1 |a iron promoter 
610 1 |a de-NOx 
610 1 |a мордениты 
610 1 |a ионный обмен 
701 1 |a Sanchez-Lopez  |b P.  |g Perla 
701 1 |a Kotolevich  |b Yu.  |g Yulia 
701 1 |a Antunez-Garcia  |b J.  |g Joel 
701 1 |a Chavez-Rivas  |b F.  |g Fernando 
701 1 |a Khramov  |b E.  |g Evgeny 
701 1 |a Berlier  |b G. 
701 1 |a Moreno-Ruiz  |b L.  |g Luis 
701 1 |a Zubavichus  |b Ya.  |g Yan 
701 1 |a Petranovskii  |b V.  |g Vitalii 
701 1 |a Fuentes-Moyado  |b S.  |g Sergio 
701 1 |a Pestryakov  |b A. N.  |c Chemist  |c Professor of Tomsk Polytechnic University, Doctor of Chemical Science  |f 1963-  |g Aleksey Nikolaevich  |3 (RuTPU)RU\TPU\pers\30471  |9 14796 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |c (2009- )  |b Исследовательская школа химических и биомедицинских технологий  |b Лаборатория "Химическая инженерия и молекулярный дизайн"  |9 26305 
801 0 |a RU  |b 63413507  |c 20230131  |g RCR 
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