Erika Bonatti, Natalia Mariano Cabral, Roshni Sajiv Kumar and Josephine M. Hill*,
{"title":"生物油升级:苯酚对琥珀酸酯醋酸酯化反应的影响","authors":"Erika Bonatti, Natalia Mariano Cabral, Roshni Sajiv Kumar and Josephine M. Hill*, ","doi":"10.1021/acs.energyfuels.5c0057710.1021/acs.energyfuels.5c00577","DOIUrl":null,"url":null,"abstract":"<p >Bio-oil is a complex organic liquid mixture generally derived from biomass pyrolysis that has potential as a sustainable fuel. Its low energy density, corrosiveness, and low stability, however, limit its use. Upgrading technologies such as the esterification of acids can be used, but the impact of the other bio-oil constituents, including phenolic compounds, on this reaction is not well understood. Thus, this work assessed the effect of phenol on the conversion of acetic acid with methanol over Amberlyst-15. At 80 °C and a methanol:acetic acid ratio of 1.6:1 (w/w), the esterification reaction happens without a catalyst in solution. The conversion was the same with or without phenol, reaching 27% after 4 h. In the presence of the solid-acid catalyst, the conversion increased to 90% over the same time. With the addition of phenol in the range of 0.06 to 0.33 (phenol-to-acetic acid mass ratio), the acid conversion decreased by 8%, while a higher ratio (0.60 w/w) had no impact on the conversion, because this higher concentration of phenol could have accelerated the regeneration of acid sites on the Amberlyst-15. A pseudo-first-order reaction in acetic acid was fit to the data and suggested that the addition of phenol did not alter the reaction mechanism. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed that phenol and acetic acid adsorb on the same sites of the Amberlyst-15 structure, but acetic acid adsorbs more strongly, which explained the decrease in the catalyst performance. X-ray photoelectron spectroscopy (XPS) confirmed catalyst surface modifications due to phenol interference. The results showed the formation of noncovalent interactions between phenol and the vinylbenzene sulfonated structure of Amberlyst-15, as well as H···π interactions under distinct environments. Overall, this study highlighted the inhibitory effects of phenol at concentrations lower than 0.60 w/w on solid-acid catalysts, providing insights for upgrading processes.</p>","PeriodicalId":35,"journal":{"name":"Energy & Fuels","volume":"39 22","pages":"10424–10434 10424–10434"},"PeriodicalIF":5.2000,"publicationDate":"2025-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bio-Oil Upgrading: Impact of Phenol on Acetic Acid Esterification with Amberlyst-15\",\"authors\":\"Erika Bonatti, Natalia Mariano Cabral, Roshni Sajiv Kumar and Josephine M. Hill*, \",\"doi\":\"10.1021/acs.energyfuels.5c0057710.1021/acs.energyfuels.5c00577\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Bio-oil is a complex organic liquid mixture generally derived from biomass pyrolysis that has potential as a sustainable fuel. Its low energy density, corrosiveness, and low stability, however, limit its use. Upgrading technologies such as the esterification of acids can be used, but the impact of the other bio-oil constituents, including phenolic compounds, on this reaction is not well understood. Thus, this work assessed the effect of phenol on the conversion of acetic acid with methanol over Amberlyst-15. At 80 °C and a methanol:acetic acid ratio of 1.6:1 (w/w), the esterification reaction happens without a catalyst in solution. The conversion was the same with or without phenol, reaching 27% after 4 h. In the presence of the solid-acid catalyst, the conversion increased to 90% over the same time. With the addition of phenol in the range of 0.06 to 0.33 (phenol-to-acetic acid mass ratio), the acid conversion decreased by 8%, while a higher ratio (0.60 w/w) had no impact on the conversion, because this higher concentration of phenol could have accelerated the regeneration of acid sites on the Amberlyst-15. A pseudo-first-order reaction in acetic acid was fit to the data and suggested that the addition of phenol did not alter the reaction mechanism. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed that phenol and acetic acid adsorb on the same sites of the Amberlyst-15 structure, but acetic acid adsorbs more strongly, which explained the decrease in the catalyst performance. X-ray photoelectron spectroscopy (XPS) confirmed catalyst surface modifications due to phenol interference. The results showed the formation of noncovalent interactions between phenol and the vinylbenzene sulfonated structure of Amberlyst-15, as well as H···π interactions under distinct environments. Overall, this study highlighted the inhibitory effects of phenol at concentrations lower than 0.60 w/w on solid-acid catalysts, providing insights for upgrading processes.</p>\",\"PeriodicalId\":35,\"journal\":{\"name\":\"Energy & Fuels\",\"volume\":\"39 22\",\"pages\":\"10424–10434 10424–10434\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-05-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Energy & Fuels\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00577\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy & Fuels","FirstCategoryId":"5","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.energyfuels.5c00577","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Bio-Oil Upgrading: Impact of Phenol on Acetic Acid Esterification with Amberlyst-15
Bio-oil is a complex organic liquid mixture generally derived from biomass pyrolysis that has potential as a sustainable fuel. Its low energy density, corrosiveness, and low stability, however, limit its use. Upgrading technologies such as the esterification of acids can be used, but the impact of the other bio-oil constituents, including phenolic compounds, on this reaction is not well understood. Thus, this work assessed the effect of phenol on the conversion of acetic acid with methanol over Amberlyst-15. At 80 °C and a methanol:acetic acid ratio of 1.6:1 (w/w), the esterification reaction happens without a catalyst in solution. The conversion was the same with or without phenol, reaching 27% after 4 h. In the presence of the solid-acid catalyst, the conversion increased to 90% over the same time. With the addition of phenol in the range of 0.06 to 0.33 (phenol-to-acetic acid mass ratio), the acid conversion decreased by 8%, while a higher ratio (0.60 w/w) had no impact on the conversion, because this higher concentration of phenol could have accelerated the regeneration of acid sites on the Amberlyst-15. A pseudo-first-order reaction in acetic acid was fit to the data and suggested that the addition of phenol did not alter the reaction mechanism. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) revealed that phenol and acetic acid adsorb on the same sites of the Amberlyst-15 structure, but acetic acid adsorbs more strongly, which explained the decrease in the catalyst performance. X-ray photoelectron spectroscopy (XPS) confirmed catalyst surface modifications due to phenol interference. The results showed the formation of noncovalent interactions between phenol and the vinylbenzene sulfonated structure of Amberlyst-15, as well as H···π interactions under distinct environments. Overall, this study highlighted the inhibitory effects of phenol at concentrations lower than 0.60 w/w on solid-acid catalysts, providing insights for upgrading processes.
期刊介绍:
Energy & Fuels publishes reports of research in the technical area defined by the intersection of the disciplines of chemistry and chemical engineering and the application domain of non-nuclear energy and fuels. This includes research directed at the formation of, exploration for, and production of fossil fuels and biomass; the properties and structure or molecular composition of both raw fuels and refined products; the chemistry involved in the processing and utilization of fuels; fuel cells and their applications; and the analytical and instrumental techniques used in investigations of the foregoing areas.