Shengbao Shi , Jianfa Chen , Lei Zhu , Tieguan Wang
{"title":"渤海湾盆地临盘油田原油中二苯并噻吩和烷基二苯并噻吩的选择性生物降解","authors":"Shengbao Shi , Jianfa Chen , Lei Zhu , Tieguan Wang","doi":"10.1016/j.jaesx.2021.100078","DOIUrl":null,"url":null,"abstract":"<div><p>The biodegradation of dibenzothiophene (DBT) and alkyl dibenzothiophenes (DBTs) were studied in crude oils from the Linpan oilfield, Bohai Bay basin, eastern China. The crude oils selected from the oilfield had been subjected to different degrees of biodegradation, i.e., non-biodegraded to severely biodegraded. With increasing biodegradation extent, the concentration of total DBTs in the crude oils rises from non- to heavily-biodegraded degrees, and then declines from heavily to severely-biodegraded degrees meanwhile the paraffins in the crude oils have been thoroughly removed. The differences in biodegradation rates had been observed between the homologues of alkyl DBTs, and the susceptibility to biodegradation of these homologues declines with increasing of the alkyl substituent number. Selective biodegradation occurred due to differences of carbon positions of alkyl substituents on molecular structure of DBTs. The sulfur-shielded isomers, such as 4,6-dimethyldibenzothiophene and 4-ethyl-6-methyldibenzothiophene, were more susceptible to biodegradation than the sulfur-exposed isomers, for example 2,8-dimethyldibenzothiophene and 1,2,7-+1,2,8-trimethyldibenzothiophenes (co-eluted as one peak in mass chromatograms). However, selective biodegradation of C<sub>4</sub>-DBTs isomers was less remarkable than the isomers of C<sub>2</sub>- and C<sub>3</sub>-DBTs, which reflected the complex processes of biodegradation.</p></div>","PeriodicalId":37149,"journal":{"name":"Journal of Asian Earth Sciences: X","volume":"7 ","pages":"Article 100078"},"PeriodicalIF":1.7000,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2590056021000359/pdfft?md5=de02f86ccbbf3ac4b7803cbf2186e953&pid=1-s2.0-S2590056021000359-main.pdf","citationCount":"2","resultStr":"{\"title\":\"Selective biodegradation of dibenzothiophene and alkyl dibenzothiophenes in crude oils from the Linpan oilfield, Bohai Bay basin, eastern China\",\"authors\":\"Shengbao Shi , Jianfa Chen , Lei Zhu , Tieguan Wang\",\"doi\":\"10.1016/j.jaesx.2021.100078\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The biodegradation of dibenzothiophene (DBT) and alkyl dibenzothiophenes (DBTs) were studied in crude oils from the Linpan oilfield, Bohai Bay basin, eastern China. The crude oils selected from the oilfield had been subjected to different degrees of biodegradation, i.e., non-biodegraded to severely biodegraded. With increasing biodegradation extent, the concentration of total DBTs in the crude oils rises from non- to heavily-biodegraded degrees, and then declines from heavily to severely-biodegraded degrees meanwhile the paraffins in the crude oils have been thoroughly removed. The differences in biodegradation rates had been observed between the homologues of alkyl DBTs, and the susceptibility to biodegradation of these homologues declines with increasing of the alkyl substituent number. Selective biodegradation occurred due to differences of carbon positions of alkyl substituents on molecular structure of DBTs. The sulfur-shielded isomers, such as 4,6-dimethyldibenzothiophene and 4-ethyl-6-methyldibenzothiophene, were more susceptible to biodegradation than the sulfur-exposed isomers, for example 2,8-dimethyldibenzothiophene and 1,2,7-+1,2,8-trimethyldibenzothiophenes (co-eluted as one peak in mass chromatograms). However, selective biodegradation of C<sub>4</sub>-DBTs isomers was less remarkable than the isomers of C<sub>2</sub>- and C<sub>3</sub>-DBTs, which reflected the complex processes of biodegradation.</p></div>\",\"PeriodicalId\":37149,\"journal\":{\"name\":\"Journal of Asian Earth Sciences: X\",\"volume\":\"7 \",\"pages\":\"Article 100078\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2022-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2590056021000359/pdfft?md5=de02f86ccbbf3ac4b7803cbf2186e953&pid=1-s2.0-S2590056021000359-main.pdf\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Asian Earth Sciences: X\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590056021000359\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GEOSCIENCES, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Asian Earth Sciences: X","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590056021000359","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GEOSCIENCES, MULTIDISCIPLINARY","Score":null,"Total":0}
Selective biodegradation of dibenzothiophene and alkyl dibenzothiophenes in crude oils from the Linpan oilfield, Bohai Bay basin, eastern China
The biodegradation of dibenzothiophene (DBT) and alkyl dibenzothiophenes (DBTs) were studied in crude oils from the Linpan oilfield, Bohai Bay basin, eastern China. The crude oils selected from the oilfield had been subjected to different degrees of biodegradation, i.e., non-biodegraded to severely biodegraded. With increasing biodegradation extent, the concentration of total DBTs in the crude oils rises from non- to heavily-biodegraded degrees, and then declines from heavily to severely-biodegraded degrees meanwhile the paraffins in the crude oils have been thoroughly removed. The differences in biodegradation rates had been observed between the homologues of alkyl DBTs, and the susceptibility to biodegradation of these homologues declines with increasing of the alkyl substituent number. Selective biodegradation occurred due to differences of carbon positions of alkyl substituents on molecular structure of DBTs. The sulfur-shielded isomers, such as 4,6-dimethyldibenzothiophene and 4-ethyl-6-methyldibenzothiophene, were more susceptible to biodegradation than the sulfur-exposed isomers, for example 2,8-dimethyldibenzothiophene and 1,2,7-+1,2,8-trimethyldibenzothiophenes (co-eluted as one peak in mass chromatograms). However, selective biodegradation of C4-DBTs isomers was less remarkable than the isomers of C2- and C3-DBTs, which reflected the complex processes of biodegradation.