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{"title":"Selective Hydrogenation of Stearic Acid to 1-Octadecanol Using Bimetallic Palladium-Tin Supported on Carbon Catalysts at Mild Reaction Conditions","authors":"Rodiansono Rodiansono, Elisa Hayati, Atina Sabila Azzahra, M. Astuti, K. Mustikasari, S. Husain, S. Sutomo","doi":"10.9767/bcrec.16.4.11895.888-903","DOIUrl":null,"url":null,"abstract":"Bimetallic palladium-tin catalysts supported on microporous carbon (denoted as Pd-Sn(x)/C, loading amount of Pd = 5 wt% and x = Pd/Sn molar ratio; c.a. 3.0; 1.5; and 1.0) showed high selectivity in the hydrogenation of stearic acid towards 1-octadecanol (stearyl alcohol) under mild reaction conditions. Pd-Sn(x)/C catalysts were synthesized via the hydrothermal method at temperature of 150 °C for 24 h, and reduced with H2 at 400 °C for 3 h. Pd-Sn(1.5)/C catalyst exhibited the highest yield of stearyl alcohol (1-octadecanol) (up to 73.2%) at 100% conversion of stearic acid at temperature 240 °C, initial H2 pressure of 3.0 MPa, a reaction time of 13 h, and in 2-propanol/water solvent. The high selectivity of alcohols over Pd-Sn(1.5)/C catalyst can be attributed to the formation of bimetallic Pd-Sn alloy phases (e.g. Pd3Sn and Pd3Sn2) as obviously depicted by XRD analysis. The presence of co-promotor Sn and the formation of bimetallic may play a pivotal role in the high selectivity of 1-octadecanol. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0). ","PeriodicalId":46276,"journal":{"name":"Bulletin of Chemical Reaction Engineering and Catalysis","volume":" ","pages":""},"PeriodicalIF":1.3000,"publicationDate":"2021-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Chemical Reaction Engineering and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9767/bcrec.16.4.11895.888-903","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
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碳负载双金属钯锡在温和反应条件下选择性加氢硬脂酸制1-十八醇
负载在微孔碳上的双金属钯-锡催化剂(表示为Pd-Sn(x)/C,Pd的负载量=5wt%和x=Pd/Sn摩尔比;c.a.3.0;1.5;和1.0)在温和的反应条件下显示出硬脂酸对1-十八醇(硬脂醇)的氢化的高选择性。在150°C的温度下,通过水热法合成了Pd-Sn(x)/C催化剂24小时,并在400°C下用H2还原3小时。在240°C、初始H2压力为3.0MPa、反应时间为13小时和2-丙醇/水溶剂中,当硬脂酸转化率为100%时,Pd-Sn(1.5)/C催化剂表现出最高的硬脂醇(1-十八醇)产率(高达73.2%)。醇在Pd-Sn(1.5)/C催化剂上的高选择性可归因于双金属Pd-Sn合金相(例如Pd3Sn和Pd3Sn2)的形成,如XRD分析所示。助催化剂Sn的存在和双金属的形成可能对1-十八醇的高选择性起着关键作用。版权所有©2021作者所有,BCREC集团出版。这是CC BY-SA许可证下的开放访问文章(https://creativecommons.org/licenses/by-sa/4.0)。
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