T. G. Harvey, T. Matheson, K. Pratt, M. Stanborough
{"title":"Rundle页岩油连续加氢处理催化剂性能研究","authors":"T. G. Harvey, T. Matheson, K. Pratt, M. Stanborough","doi":"10.1021/I200033A029","DOIUrl":null,"url":null,"abstract":"The 100-400C fraction of Rundle shale oil has been processed over three commercial sulfide hydrotreating catalysts at 400C, 13.8-MPa hydrogen pressure, and 1.0-h/sup -1/ LHSV. Ni-W/SiO/sub 2/-Al/sub 2/O/sub 3/ deactivated rapidly, Co-Mo/Al/sub 2/O/sub 3/ was effective, and Ni-Mo/Al/sub 2/O/sub 3/ was most effective. The Ni-Mo should allow production of a good substitute crude oil but not single-step production of finished middle-distillate fuels. Hydroprocessing under the above conditions did not alter the boiling range of the oil much, but all the catalysts brought about hydrogenation of diaromatic material, a concomitant increase in hydroaromatics, and some cracking of polyaromatics. All the catalysts except the Ni-W completely deoxygenated phenolic components. Residual nitrogen compounds were predominantly nonbasic benzo- and dibenzopyrroles.","PeriodicalId":13537,"journal":{"name":"Industrial & Engineering Chemistry Process Design and Development","volume":"31 1","pages":"521-527"},"PeriodicalIF":0.0000,"publicationDate":"1986-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"8","resultStr":"{\"title\":\"Catalyst performance in continuous hydrotreating of Rundle shale oil\",\"authors\":\"T. G. Harvey, T. Matheson, K. Pratt, M. Stanborough\",\"doi\":\"10.1021/I200033A029\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The 100-400C fraction of Rundle shale oil has been processed over three commercial sulfide hydrotreating catalysts at 400C, 13.8-MPa hydrogen pressure, and 1.0-h/sup -1/ LHSV. Ni-W/SiO/sub 2/-Al/sub 2/O/sub 3/ deactivated rapidly, Co-Mo/Al/sub 2/O/sub 3/ was effective, and Ni-Mo/Al/sub 2/O/sub 3/ was most effective. The Ni-Mo should allow production of a good substitute crude oil but not single-step production of finished middle-distillate fuels. Hydroprocessing under the above conditions did not alter the boiling range of the oil much, but all the catalysts brought about hydrogenation of diaromatic material, a concomitant increase in hydroaromatics, and some cracking of polyaromatics. All the catalysts except the Ni-W completely deoxygenated phenolic components. Residual nitrogen compounds were predominantly nonbasic benzo- and dibenzopyrroles.\",\"PeriodicalId\":13537,\"journal\":{\"name\":\"Industrial & Engineering Chemistry Process Design and Development\",\"volume\":\"31 1\",\"pages\":\"521-527\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1986-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"8\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Industrial & Engineering Chemistry Process Design and Development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1021/I200033A029\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial & Engineering Chemistry Process Design and Development","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/I200033A029","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Catalyst performance in continuous hydrotreating of Rundle shale oil
The 100-400C fraction of Rundle shale oil has been processed over three commercial sulfide hydrotreating catalysts at 400C, 13.8-MPa hydrogen pressure, and 1.0-h/sup -1/ LHSV. Ni-W/SiO/sub 2/-Al/sub 2/O/sub 3/ deactivated rapidly, Co-Mo/Al/sub 2/O/sub 3/ was effective, and Ni-Mo/Al/sub 2/O/sub 3/ was most effective. The Ni-Mo should allow production of a good substitute crude oil but not single-step production of finished middle-distillate fuels. Hydroprocessing under the above conditions did not alter the boiling range of the oil much, but all the catalysts brought about hydrogenation of diaromatic material, a concomitant increase in hydroaromatics, and some cracking of polyaromatics. All the catalysts except the Ni-W completely deoxygenated phenolic components. Residual nitrogen compounds were predominantly nonbasic benzo- and dibenzopyrroles.