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CoMo/Al2O3 Hydrodesulfurization Catalyst Modified with Nitrilotriacetic Acid: Preparation Without Use of NH4+ and NO3− Ions.
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SYSNO ASEP 0556449 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title CoMo/Al2O3 Hydrodesulfurization Catalyst Modified with Nitrilotriacetic Acid: Preparation Without Use of NH4+ and NO3− Ions. Author(s) Zdražil, Miroslav (UCHP-M) RID, SAI
Kaluža, Luděk (UCHP-M) RID, ORCID, SAISource Title Catalysis Letters - ISSN 1011-372X
Roč. 153, č. 1 (2023), s. 311-319Number of pages 9 s. Language eng - English Country US - United States Keywords CoMo/Al2O3 ; hydrodesulfurization ; nitrilotriacetic acid ; thiophene HDS Subject RIV CF - Physical ; Theoretical Chemistry OECD category Physical chemistry R&D Projects GA17-22490S GA ČR - Czech Science Foundation (CSF) TN01000048 GA TA ČR - Technology Agency of the Czech Republic (TA ČR) Method of publishing Limited access Institutional support UCHP-M - RVO:67985858 UT WOS 000772548600001 EID SCOPUS 85126841009 DOI 10.1007/s10562-022-03984-7 Annotation Impregnation solutions for the preparation of NTA-modified CoMo/Al2O3 hydrodesulfurization catalysts were prepared without use of unnecessary and disrupting NH4+ and NO3− ions. The reaction-dissolution took place in the suspension of NTA, CoCO3·xH2O and MoO3 (here DISUSPEN method). The conventional solutions, prepared in the literature using NTA, NH4OH, MoO3 and Co(NO3)2, (here DISAMON method), were neutral or basic. The solid obtained by their drying was partly crystalline. The DISUSPEN solutions were acidic, with pH = 1.0–1.5. The DISUSPEN solids were XRD-amorphous with glass-like appearance. Much less nitrogen-containing emissions is produced during in-situ sulfidation of DISUSPEN catalysts as compared with DISAMON catalysts. Catalysts prepared by the DISUSPEN method are more active in HDS of thiophene than those prepared by the conventional DISAMON method. Workplace Institute of Chemical Process Fundamentals Contact Eva Jirsová, jirsova@icpf.cas.cz, Tel.: 220 390 227 Year of Publishing 2024 Electronic address http://hdl.handle.net/11104/0330790
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