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A New Method for Producing Substituted Anthraquinones via Diene Synthesis in the Presence of Mo-V-P Heteropoly Acid Solution: Catalyst Regeneration Full article

Journal Catalysis in Industry
ISSN: 2070-0504 , E-ISSN: 2070-0555
Output data Year: 2016, Volume: 8, Number: 4, Pages: 310-315 Pages count : 6 DOI: 10.1134/S2070050416040048
Tags heteropoly acid, regeneration, substituted anthraquinones
Authors Gogin L.L. 1 , Zhizhina E.G. 1 , Pai Z.P. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Funding (1)

1 Federal Agency for Scientific Organizations V.44.2.8.

Abstract: The possibilities of developing catalytic processes for the synthesis of 2-methylanthraquinone from 1,4-naphthaquinone (NQ) and isoprene, and synthesizing 2,3-dimethylanthraquinone from NQ and 2,3-dimethylbutadiene in the presence of aqueous solutions of high-vanadium heteropoly acid (HPA) as a bifunctional catalyst are examined. Two methods for catalyst regeneration are discussed: oxidation with oxygen at = 0.3–0.4 MPa and with concentrated nitric acid at atmosphere pressure. It is shown that regeneration with nitric acid ensures deeper oxidation of the reduced catalyst. Complete restoration of the properties of the catalyst following regeneration offers the possibility of its repeated use in the processes discussed in this work
Cite: Gogin L.L. , Zhizhina E.G. , Pai Z.P.
A New Method for Producing Substituted Anthraquinones via Diene Synthesis in the Presence of Mo-V-P Heteropoly Acid Solution: Catalyst Regeneration
Catalysis in Industry. 2016. V.8. N4. P.310-315. DOI: 10.1134/S2070050416040048 WOS Scopus РИНЦ OpenAlex
Original: Гогин Л.Л. , Жижина Е.Г. , Пай З.П.
Новый способ производства замещенных антрахинонов через диеновый синтез в присутствии раствора Mo-V-P гетерополикислоты: регенерация катализатора
Катализ в промышленности. 2016. Т.16. №3. С.24-30. DOI: 10.18412/1816-0387-2016-3-24-30 РИНЦ ANCAN OpenAlex
Dates:
Submitted: Apr 18, 2016
Published print: Oct 1, 2016
Published online: Dec 28, 2016
Identifiers:
Web of science: WOS:000390991400004
Scopus: 2-s2.0-85007047593
Elibrary: 29466297
OpenAlex: W2397343132
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 3
OpenAlex 1
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