Solid Acid Resin Amberlyst 45 as a Catalyst for the Transesterification of Vegetable Oil

被引:21
|
作者
Cabral, Natalia Mariano [1 ]
Lorenti, Juliana P. [1 ]
Plass, Winfried [2 ]
Gallo, Jean Marcel R. [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Chem, Grp Renewable Energy Nanotechnol & Catalysis Gree, Sao Carlos, Brazil
[2] Friedrich Schiller Univ Jena, Inst Inorgan & Analyt Chem, Jena, Germany
来源
FRONTIERS IN CHEMISTRY | 2020年 / 8卷
基金
巴西圣保罗研究基金会;
关键词
biodiesel; transesterification; ethanolysis; Amberlyst; 45; acid catalysis; ION-EXCHANGE RESINS; WASTE COOKING OIL; BIODIESEL PRODUCTION; DIETHYL-ETHER; CALCIUM-OXIDE; RAPESEED OIL; SOYBEAN OIL; FATTY-ACID; PALM OIL; ESTERIFICATION;
D O I
10.3389/fchem.2020.00305
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Commercial transesterification of vegetable oil to biodiesel using alkaline hydroxides requires expensive refined vegetable oil and anhydrous alcohols to avoid saponification. These issues are not present in the acid-catalyzed process; however, the challenge still lies in developing stable and active solid acid catalysts. Herein, Amberlyst 45, a resin for high-temperature application, was efficiently used for biodiesel production by the methanolysis or ethanolysis of vegetable oil. Yields of up to 80 and 84% were obtained for the fatty acid methyl ester and the fatty acid ethyl ester, respectively. Two processes are proposed and showed to be efficient: (i) incremental addition of alcohol along with the reaction for both methanolysis and ethanolysis; or (ii) one-pot reaction for ethanolysis using oil/ethanol molar ratio of 1/18. The catalytic system used also showed to be compatible with used oil (2.48 +/- 0.03 mg(NaOH)g(oil)(-1)) and to the presence of water (10-20 wt. % based on the alcohol), allowing the use of waste oil and hydrated alcohol.
引用
收藏
页数:10
相关论文
共 50 条
  • [21] Transesterification of jatropha oil using a mixture of natural shells as solid catalyst
    Eswararao, Y.
    Niju, S.
    Begum, K. M. Meera Sheriffa
    Anantharaman, N.
    Raj, S. Malik
    BIOFUELS-UK, 2016, 7 (04): : 345 - 351
  • [22] Application of dolomite as solid base catalyst for transesterification of rapeseed oil with butanol
    Gaide, Ieva
    Makareviciene, Violeta
    Sendzikiene, Egle
    Gumbyte, Milda
    SUSTAINABLE ENERGY TECHNOLOGIES AND ASSESSMENTS, 2022, 52
  • [23] Transesterification of soybean oil to biodiesel using SrO as a solid base catalyst
    Liu, Xuejun
    He, Huayang
    Wang, Yujun
    Zhu, Shenlin
    CATALYSIS COMMUNICATIONS, 2007, 8 (07) : 1107 - 1111
  • [24] Calcium ethoxide as a solid base catalyst for the transesterification of soybean oil to biodiesel
    Liu, Xuejun
    Piao, Xianglan
    Wang, Yujun
    Zhu, Shenfin
    ENERGY & FUELS, 2008, 22 (02) : 1313 - 1317
  • [25] A new solid base catalyst for the transesterification of rapeseed oil to biodiesel with methanol
    Wang, Boyang
    Li, Shufen
    Tian, Songjiang
    Feng, Rihua
    Meng, Yonglu
    FUEL, 2013, 104 : 698 - 703
  • [26] Magnetic solid acid catalyst in preparation of high hydroxyl vegetable oil-based polyols
    Wang, Hanying
    Jiang, Pingping
    Liu, Dekai
    Nie, Zhixin
    Deng, Jianneng
    Cao, Zhiliang
    Jingxi Huagong/Fine Chemicals, 2020, 37 (09): : 1847 - 1853
  • [27] Transesterification of Soybean Oil to Biodiesel over Heterogeneous Solid Base Catalyst
    Teng, Guangyuan
    Gao, Lijing
    Xiao, Guomin
    Liu, Hu
    ENERGY & FUELS, 2009, 23 (09) : 4630 - 4634
  • [28] Transesterification of castor oil to biodiesel using CaO as a solid base catalyst
    Jin, Fu-Quan
    Niu, Yu-Lan
    Li, Bing
    Li, Xiao-Hong
    Shiyou Huagong Gaodeng Xuexiao Xuebao/Journal of Petrochemical Universities, 2008, 21 (03): : 53 - 56
  • [29] Synthesis of levulinic acid from fructose using Amberlyst-15 as a solid acid catalyst
    Pham Anh Son
    Shun Nishimura
    Kohki Ebitani
    Reaction Kinetics, Mechanisms and Catalysis, 2012, 106 : 185 - 192
  • [30] Synthesis of levulinic acid from fructose using Amberlyst-15 as a solid acid catalyst
    Son, Pham Anh
    Nishimura, Shun
    Ebitani, Kohki
    REACTION KINETICS MECHANISMS AND CATALYSIS, 2012, 106 (01) : 185 - 192