L. F. Sayfulina, E. A. Buluchevskiy, A. Lavrenov, A. Arbuzov, T. R. Karpova
{"title":"PdO-Re2O7/SO42-/ZrO2-Al2O3催化剂在乙烯直接合成丙烯中的稳定性","authors":"L. F. Sayfulina, E. A. Buluchevskiy, A. Lavrenov, A. Arbuzov, T. R. Karpova","doi":"10.1063/1.5122910","DOIUrl":null,"url":null,"abstract":"During tests of palladium-rhenium catalysts based on sulfated zirconia in the process of direct synthesis of propylene from ethylene, it was found out that modifying the support with γ-Al2O3 increases significantly the stability of the system. Multi-cycle tests showed that systems with alumina content of 20 and 40 wt. % maintain its activity during a few tens of hours at the level of 50-80 %. The propylene yield from cycle to cycle remains practically unchanged (28-35 wt. %). According to UV spectroscopy and GLC with MSD, changes in the palladium and rhenium valence state don’t occur during the catalysts operation. The catalyst deactivation is caused by the C8+ oligomers deposit on its surface resulting from secondary processes of butenes oligomerization on the catalyst acid sites and C6+ hydrocarbons metathesis.","PeriodicalId":177536,"journal":{"name":"21ST CENTURY: CHEMISTRY TO LIFE","volume":"2 5 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Stability of PdO-Re2O7/SO42-/ZrO2-Al2O3 catalyst for direct synthesis of propylene from ethylene\",\"authors\":\"L. F. Sayfulina, E. A. Buluchevskiy, A. Lavrenov, A. Arbuzov, T. R. Karpova\",\"doi\":\"10.1063/1.5122910\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"During tests of palladium-rhenium catalysts based on sulfated zirconia in the process of direct synthesis of propylene from ethylene, it was found out that modifying the support with γ-Al2O3 increases significantly the stability of the system. Multi-cycle tests showed that systems with alumina content of 20 and 40 wt. % maintain its activity during a few tens of hours at the level of 50-80 %. The propylene yield from cycle to cycle remains practically unchanged (28-35 wt. %). According to UV spectroscopy and GLC with MSD, changes in the palladium and rhenium valence state don’t occur during the catalysts operation. The catalyst deactivation is caused by the C8+ oligomers deposit on its surface resulting from secondary processes of butenes oligomerization on the catalyst acid sites and C6+ hydrocarbons metathesis.\",\"PeriodicalId\":177536,\"journal\":{\"name\":\"21ST CENTURY: CHEMISTRY TO LIFE\",\"volume\":\"2 5 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-08-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"21ST CENTURY: CHEMISTRY TO LIFE\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1063/1.5122910\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"21ST CENTURY: CHEMISTRY TO LIFE","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1063/1.5122910","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Stability of PdO-Re2O7/SO42-/ZrO2-Al2O3 catalyst for direct synthesis of propylene from ethylene
During tests of palladium-rhenium catalysts based on sulfated zirconia in the process of direct synthesis of propylene from ethylene, it was found out that modifying the support with γ-Al2O3 increases significantly the stability of the system. Multi-cycle tests showed that systems with alumina content of 20 and 40 wt. % maintain its activity during a few tens of hours at the level of 50-80 %. The propylene yield from cycle to cycle remains practically unchanged (28-35 wt. %). According to UV spectroscopy and GLC with MSD, changes in the palladium and rhenium valence state don’t occur during the catalysts operation. The catalyst deactivation is caused by the C8+ oligomers deposit on its surface resulting from secondary processes of butenes oligomerization on the catalyst acid sites and C6+ hydrocarbons metathesis.