{"title":"Decarboxylation of oleic acid using iridium catalysis to form products of increased aromatic content compared to ruthenium systems","authors":"K. Doll, B. Moser, G. Knothe","doi":"10.1080/19397038.2021.1978589","DOIUrl":null,"url":null,"abstract":"ABSTRACT The decarboxylation of 9-cis-octadecenoic (oleic) acid to aromatic and aliphatic hydrocarbons suitable as blend components for aviation fuel applications utilising ruthenium dodecacarbonyl [Ru3(CO)12] with a variety of other catalysts is presented. Due to the different relative rates of decarboxylation and hydrogenation/dehydrogenation, different product distributions are possible when the catalyst is varied. Chloro-1,5-cyclooctadiene iridium (I) dimer [(C8H12IrCl)2] gave a similar conversion to the ruthenium system but provided an altered product distribution. Aromatic contents of up to 35% were achieved in the iridium system, thereby providing a wider range of blending options for fuel producers. Additionally, both catalytic systems were found to decarboxylate high-oleic soybean oil fatty acids, giving a product of similar energy content to that obtained using high grade oleic acid.","PeriodicalId":14400,"journal":{"name":"International Journal of Sustainable Engineering","volume":"14 1","pages":"2018 - 2024"},"PeriodicalIF":3.6000,"publicationDate":"2021-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Sustainable Engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/19397038.2021.1978589","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 2
Abstract
ABSTRACT The decarboxylation of 9-cis-octadecenoic (oleic) acid to aromatic and aliphatic hydrocarbons suitable as blend components for aviation fuel applications utilising ruthenium dodecacarbonyl [Ru3(CO)12] with a variety of other catalysts is presented. Due to the different relative rates of decarboxylation and hydrogenation/dehydrogenation, different product distributions are possible when the catalyst is varied. Chloro-1,5-cyclooctadiene iridium (I) dimer [(C8H12IrCl)2] gave a similar conversion to the ruthenium system but provided an altered product distribution. Aromatic contents of up to 35% were achieved in the iridium system, thereby providing a wider range of blending options for fuel producers. Additionally, both catalytic systems were found to decarboxylate high-oleic soybean oil fatty acids, giving a product of similar energy content to that obtained using high grade oleic acid.