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Production of Oxygenated Fuel Additives from Residual Glycerine Using Biocatalysts Obtained from Heavy-Metal-Contaminated Jatropha curcas L. Roots

机译:使用从重金属污染的麻醉药Curcas L. Roots获得的生物催化剂,从残留甘油的生产中氧化燃料添加剂

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摘要

This work aims to shed light on the use of two biochars, obtained from the pyrolysis at 550 °C of heavy-metal-contaminated Jatropha curcas L. roots, as heterogeneous catalysts for glycerol esterification using residual glycerine. To do this, glycerine from biodiesel production was purified. In a first step, H3PO4 or H2SO4 was used to remove non-glycerol organic matter. The glycerol-rich phase was then extracted with ethanol or propanol, which increased the glycerol content from 43.2% to up to 100%. Subsequently, the esterification of both purified glycerine and commercial USP glycerine was assayed with acetic acid (AA) or with acetic anhydride (AH) at 9:1 molar ratio to glycerol using Amberlyst-15 as catalyst. Different reaction times (from 1.5 to 3 h) and temperatures (100⁻115 °C when using AA and 80⁻135 °C when using AH) were assessed. Results revealed that the most suitable conditions were 80 °C and 1.5 h reaction time using AH, achieving 100% yield and selectivity towards triacetylglycerol (TAG) almost with both glycerines. Finally, the performance and reuse of the two heterogeneous biocatalysts was assessed. Under these conditions, one of the biocatalysts also achieved 100% TAG yield.
机译:这项工作旨在阐明使用两种生物脉,从550°C的重金系统污染的麻醉药Curcas1.根系中获得的热解,作为使用残余甘油的甘油酯化的异构催化剂。为此,纯化来自生物柴油生产的甘油。在第一步中,使用H3PO4或H 2 SO 4去除非甘油有机物质。然后用乙醇或丙醇萃取富含甘油的相,该丙醇将甘油含量增加到43.2%至高达100%。随后,使用Amberlyst-15作为催化剂,用乙酸(AA)或用乙酸(AA)或乙酸酐(AH)的乙酸(AH)或乙酸酐(AH)和乙酸酐(AH)和乙酸酐(AH)的酯化进行测定。评估不同的反应时间(从1.5至3小时)和温度(在使用AA和80℃和80℃时使用AH)的温度。结果表明,最合适的条件为80℃和1.5小时反应时间,使用均匀达到100%产率和选择性,朝向三乙酰甘油(标签)与甘油。最后,评估了两个异质生物催化剂的性能和再利用。在这些条件下,其中一种生物催化剂也达到了100%标签产量。

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