{"title":"废食用油转化为高级化学品的金属氧化物催化剂的比较研究","authors":"Wali Ullah, N. A. Khan, N. H. Syed, M. Habib","doi":"10.21743/pjaec/2021.06.15","DOIUrl":null,"url":null,"abstract":"Cracking of edible oils occurs at high temperature and forms valued low molecular weight chemical species. The aim of the current study was to find a catalyst which can break these heavy molecules at the lower ranges of temperatures. From the analysis prospective, the non-condensable hydrocarbons (gaseous product species) were not determined and reactions study was carried out in a batch reactor. There was no evident conversion up to a temperature of 450 °C in the absence of catalyst whereas the reaction mixture was left inside a batch reactor for a long duration of an hour. Reaction parameters, such as catalyst types (ZnO and Al2O3), amount of catalyst, reaction temperature, residence or holding time, and heating rate to reach a reaction temperature were systematically examined. Powdered form of catalyst samples (ZnO and Al2O3) were characterized by using XRD, EDX, and Nitrogen adsorption isotherms. Temperatures studied over ZnO catalyst were 400 °C, 425 °C, 450 °C, 475 °C, and 500 °C. The maximum oil conversion was 81 % at a temperature of 450 °C. We observed that the conversion increases from 400 °C to 450 °C, whereas above 450 °C it starts to decrease. However, in comparison to ZnO catalyst the reaction rate was much higher over the Al2O3, i.e. a considerable conversion occurred at lower ranges of temperatures. Thus here a different set of temperatures (330 °C, 370 °C, 390 °C, 410 °C, and 430°C) were used. When reacting for an hour at a temperature of 390 °C, and in the presence of 8 wt.% of Al2O3 (same catalyst mass was used in ZnO reacting system) the conversion reached to 71 %. Above 390 °C the conversion decreased. Over both tested metal oxide catalysts the caloric value, density, flash point, and kinematic viscosity of the liquid product species were similar to petro fuels. The XRD and EDX signature of the catalyst samples corresponds to the standard ZnO and Al2O3 patterns. Finally, when compared to ZnO the better activity over the Al2O3 (higher conversion at lower temperature) catalyst can be linked with a high external surface area.","PeriodicalId":19846,"journal":{"name":"Pakistan Journal of Analytical & Environmental Chemistry","volume":null,"pages":null},"PeriodicalIF":0.4000,"publicationDate":"2021-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A Comparison Study of the Metal Oxide Catalysts for the Conversion of Used Cooking Oil into High Grade Chemicals\",\"authors\":\"Wali Ullah, N. A. Khan, N. H. Syed, M. Habib\",\"doi\":\"10.21743/pjaec/2021.06.15\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cracking of edible oils occurs at high temperature and forms valued low molecular weight chemical species. The aim of the current study was to find a catalyst which can break these heavy molecules at the lower ranges of temperatures. From the analysis prospective, the non-condensable hydrocarbons (gaseous product species) were not determined and reactions study was carried out in a batch reactor. There was no evident conversion up to a temperature of 450 °C in the absence of catalyst whereas the reaction mixture was left inside a batch reactor for a long duration of an hour. Reaction parameters, such as catalyst types (ZnO and Al2O3), amount of catalyst, reaction temperature, residence or holding time, and heating rate to reach a reaction temperature were systematically examined. Powdered form of catalyst samples (ZnO and Al2O3) were characterized by using XRD, EDX, and Nitrogen adsorption isotherms. Temperatures studied over ZnO catalyst were 400 °C, 425 °C, 450 °C, 475 °C, and 500 °C. The maximum oil conversion was 81 % at a temperature of 450 °C. We observed that the conversion increases from 400 °C to 450 °C, whereas above 450 °C it starts to decrease. However, in comparison to ZnO catalyst the reaction rate was much higher over the Al2O3, i.e. a considerable conversion occurred at lower ranges of temperatures. Thus here a different set of temperatures (330 °C, 370 °C, 390 °C, 410 °C, and 430°C) were used. When reacting for an hour at a temperature of 390 °C, and in the presence of 8 wt.% of Al2O3 (same catalyst mass was used in ZnO reacting system) the conversion reached to 71 %. Above 390 °C the conversion decreased. Over both tested metal oxide catalysts the caloric value, density, flash point, and kinematic viscosity of the liquid product species were similar to petro fuels. The XRD and EDX signature of the catalyst samples corresponds to the standard ZnO and Al2O3 patterns. Finally, when compared to ZnO the better activity over the Al2O3 (higher conversion at lower temperature) catalyst can be linked with a high external surface area.\",\"PeriodicalId\":19846,\"journal\":{\"name\":\"Pakistan Journal of Analytical & Environmental Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.4000,\"publicationDate\":\"2021-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Pakistan Journal of Analytical & Environmental Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21743/pjaec/2021.06.15\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pakistan Journal of Analytical & Environmental Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21743/pjaec/2021.06.15","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
A Comparison Study of the Metal Oxide Catalysts for the Conversion of Used Cooking Oil into High Grade Chemicals
Cracking of edible oils occurs at high temperature and forms valued low molecular weight chemical species. The aim of the current study was to find a catalyst which can break these heavy molecules at the lower ranges of temperatures. From the analysis prospective, the non-condensable hydrocarbons (gaseous product species) were not determined and reactions study was carried out in a batch reactor. There was no evident conversion up to a temperature of 450 °C in the absence of catalyst whereas the reaction mixture was left inside a batch reactor for a long duration of an hour. Reaction parameters, such as catalyst types (ZnO and Al2O3), amount of catalyst, reaction temperature, residence or holding time, and heating rate to reach a reaction temperature were systematically examined. Powdered form of catalyst samples (ZnO and Al2O3) were characterized by using XRD, EDX, and Nitrogen adsorption isotherms. Temperatures studied over ZnO catalyst were 400 °C, 425 °C, 450 °C, 475 °C, and 500 °C. The maximum oil conversion was 81 % at a temperature of 450 °C. We observed that the conversion increases from 400 °C to 450 °C, whereas above 450 °C it starts to decrease. However, in comparison to ZnO catalyst the reaction rate was much higher over the Al2O3, i.e. a considerable conversion occurred at lower ranges of temperatures. Thus here a different set of temperatures (330 °C, 370 °C, 390 °C, 410 °C, and 430°C) were used. When reacting for an hour at a temperature of 390 °C, and in the presence of 8 wt.% of Al2O3 (same catalyst mass was used in ZnO reacting system) the conversion reached to 71 %. Above 390 °C the conversion decreased. Over both tested metal oxide catalysts the caloric value, density, flash point, and kinematic viscosity of the liquid product species were similar to petro fuels. The XRD and EDX signature of the catalyst samples corresponds to the standard ZnO and Al2O3 patterns. Finally, when compared to ZnO the better activity over the Al2O3 (higher conversion at lower temperature) catalyst can be linked with a high external surface area.