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Transformation of Petroleum Asphaltenes in Supercritical Alcohols Studied via FTIR and NMR Techniques Научная публикация

Журнал Energy and Fuels
ISSN: 0887-0624 , E-ISSN: 1520-5029
Вых. Данные Год: 2018, Том: 32, Номер: 2, Страницы: 2117-2127 Страниц : 11 DOI: 10.1021/acs.energyfuels.7b01630
Ключевые слова MAGNETIC-RESONANCE-SPECTROSCOPY; VAPOR-PRESSURE OSMOMETRY; ELECTRON-SPIN-RESONANCE; CRUDE OILS; VACUUM RESIDUE; HEAVY OILS; IN-SITU; PARTIAL OXIDATION; STRUCTURAL-CHARACTERIZATION; BITUMEN CRACKING
Авторы Chibiryaev Andrey M. 1,2 , Kozhevnikov Ivan V. 1 , Shalygin Anton S. 1 , Martyanov Oleg N. 1,2
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Academician Lavrentiev Avenue 5, 630090 Novosibirsk, Russia
2 Novosibirsk State University, Pirogov Street 1, 630090 Novosibirsk, Russia

Информация о финансировании (1)

1 Российский научный фонд 15-19-00119

Реферат: The aliphatic alcohols (methanol, ethanol, 1- and 2-propanols) were used for the first time as a reaction media for the upgrading of crude oil asphaltenes. The process was realized in a batch reactor under supercritical conditions (at 350○C). The three main fractions of the products (hexane- and benzene-soluble fractions (HSF and BSF) and insoluble residue (IR)) were analyzed using ATR-FTIR and 1H/13C NMR spectroscopy to characterize structural changes of the initial asphaltenes (IA). According to NMR data, the aliphatics are the main part of the HSF and BSF. The alcohols were appeared to influence the content of both aliphatics and aromatics in the products. The content of aliphatics in the HSF increases in the line from “lighter” to “heavier” alcohols used, but reduces in the BSF. However the content of aromatics in the HSF increases from “heavier” to “lighter” alcohols while this order is reversed for the BSF. According to the ATR-FTIR spectroscopy data, the aromatics/aliphatics ratios observed for the insoluble residues are 2–3 times higher as compared with the initial asphaltenes, but two times lower for the HSF. The BSF are composed of less condensed aromatics than those of the IA. It is shown that the alcohols used as a reaction media are incorporated in the product molecules as alkoxy substituents in aromatic ethers Ar–OAlk. According to NMR and ATR-FTIR data obtained, the alkylation/dealkylation and alkoxylation reactions make a crucial contribution to the chemical transformations of the asphaltenes.
Библиографическая ссылка: Chibiryaev A.M. , Kozhevnikov I.V. , Shalygin A.S. , Martyanov O.N.
Transformation of Petroleum Asphaltenes in Supercritical Alcohols Studied via FTIR and NMR Techniques
Energy and Fuels. 2018. V.32. N2. P.2117-2127. DOI: 10.1021/acs.energyfuels.7b01630 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 7 июн. 2017 г.
Принята к публикации: 19 окт. 2017 г.
Опубликована online: 31 окт. 2017 г.
Опубликована в печати: 15 февр. 2018 г.
Идентификаторы БД:
Web of science: WOS:000426015000116
Scopus: 2-s2.0-85042186823
РИНЦ: 35488602
Chemical Abstracts: 2017:1701586
Chemical Abstracts (print): 168:181506
OpenAlex: W2765434177
Цитирование в БД:
БД Цитирований
Web of science 29
Scopus 31
РИНЦ 29
OpenAlex 30
Альметрики: