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New Way of Hydroquinone and Catechol Synthesis using Nitrous Oxide as Oxidant Научная публикация

Журнал Advanced Synthesis and Catalysis
ISSN: 1615-4150 , E-ISSN: 1615-4169
Вых. Данные Год: 2002, Том: 344, Номер: 9, Страницы: 986-995 Страниц : 10 DOI: 10.1002/1615-4169(200210)344:9<986::AID-ADSC986>3.0.CO;2-N
Ключевые слова Benzene oxidation, Dihydroxybenzenes, Iron, Nitrous oxide, Phenol oxidation, Zeolite
Авторы Ivanov D.P. 1 , Sobolev V.I. 1 , Pirutko L.V. 1 , Panov G.I. 1
Организации
1 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russia

Реферат: The synthesis of dihydroxybenzenes (DHB) via the gas-phase oxidation of phenol with nitrous oxide in the presence of benzene was studied. Addition of benzene to the feed mixture greatly improves the selectivity and catalytic stability of the Fe-containing ZSM-5 zeolite, that was previously considered to be a main obstacle to the development of a new process. Reaction conditions strongly affect the distribution of the DHB isomers: the ratio of hydroquinone to catechol may vary from 1.4 to 10, with the resorcinol fraction being nearly constant and comprising 3–5%. Some 40 h experiments on the oxidation of a phenol-benzene mixture demonstrated the high efficiency of the formed FeZSM-5 catalyst. With a good stability, the catalyst provides 97% phenol selectivity referred to DHB and 85–90% N2O selectivity referred to the sum of DHBs and phenol. A new process for hydroquinone and catechol synthesis based on the neat oxidation of benzene with recycling of the phenol as an intermediate product is suggested.
Библиографическая ссылка: Ivanov D.P. , Sobolev V.I. , Pirutko L.V. , Panov G.I.
New Way of Hydroquinone and Catechol Synthesis using Nitrous Oxide as Oxidant
Advanced Synthesis and Catalysis. 2002. V.344. N9. P.986-995. DOI: 10.1002/1615-4169(200210)344:9<986::AID-ADSC986>3.0.CO;2-N WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 21 мая 2002 г.
Принята к публикации: 16 июл. 2002 г.
Опубликована в печати: 1 окт. 2002 г.
Опубликована online: 28 окт. 2002 г.
Идентификаторы БД:
Web of science: WOS:000179051900012
Scopus: 2-s2.0-0242460885
РИНЦ: 13405900
Chemical Abstracts: 2002:858580
Chemical Abstracts (print): 138:108632
OpenAlex: W2146985275
Цитирование в БД:
БД Цитирований
Web of science 22
Scopus 27
РИНЦ 25
OpenAlex 25
Альметрики: