期刊文献+

固体酸催化大豆油与乙醇酯交换制备生物柴油 被引量:24

Transesterification of Soybean Oil With Ethanol to Biodiesel Using Solid Acid Catalyst
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摘要 利用淀粉和对甲基苯磺酸合成了新型碳基固体酸催化剂,并将它应用于大豆油与乙醇的酯交换反应制备生物柴油。考察了反应时间、反应温度、醇油摩尔比、催化剂用量及使用次数等因素对生物柴油收率的影响。结果表明,新型碳基固体酸催化剂对大豆油与乙醇酯交换反应有很高的催化活性,易于分离,具有良好的稳定性。最佳反应条件为:醇油摩尔比为8∶1,催化剂质量分数为7.0%,反应时间8 h,反应温度为80℃,该条件下生物柴油的质量收率可达67.4%。 New carbon-based solid acid catalyst was synthesized from starch and p--toluene sulfonic acid,and applied for the preparation of biodiesel with soybean oil and ethanol. The effect of reaction conditions such as the reaction time, reaction temperature, the molar ratio of ethanol with soybean oil, the amount of catalyst to the yield of biodiesel was investigated. The new carbon--based solid acid catalyst shows high catalytic activity and good stability, and can easily be separated from the products. The optimal conditions are: the molar ratio of ethanol to soybean oil 8:1, the amount of catalyst is the quality of soybean oil 7.0% (w), reaction time 8 h , reaction temperature 80℃. Under optimum condition, the yield of biodiesel could reach 67.4%.
出处 《辽宁石油化工大学学报》 CAS 2008年第2期4-7,共4页 Journal of Liaoning Petrochemical University
基金 辽宁省教育厅资助项目(05L299)
关键词 碳基固体酸 酯交换 生物柴油 淀粉 对甲基苯磺酸 Carbon--based solid acid Transesterification Biodiesel Starch P-toluene sulfonic acid
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参考文献12

  • 1Edgar L, James G G, David A B, et al. The catalysis of biodiesel synthesis[J]. Catalysis, 2006(19 ):41-83. 被引量:1
  • 2Edgar L, Liu Y J, Dora E L, et al. Synthesis of biodiesel via acid catalysis[J]. Industrial & engineering chemistry research, 2005,44 (14):5353-5363. 被引量:1
  • 3Mangesh G K, Ajay K D. Waste cooking oils an economical source for biodiesel: A review[J]. Industrial & engineering chemistry research, 2006,45 (9) : 2901- 2913. 被引量:1
  • 4Hara M, Yoshida T, Takagaki A, et al. A carbon material as a strong protonic acid[J]. Angew. chem. int. ed. , 2004, 116(22) : 3015-3018. 被引量:1
  • 5Toda M, Takagaki A, Okamura M, et al. Green chemistry: Bio-diesel made with sugar catalyst[J]. Nature, 2005, 438 (382): 178-179. 被引量:1
  • 6Okamura M, Takagaki A, Toda M, et al. Acid-catalyzed reactions on flexible polycyclic aromatic carbon in amorphous carbon. Chem.[J]. Mater., 2006, 18(13): 3039-3045. 被引量:1
  • 7高珊,梁学正,王雯娟,程文萍,杨建国.新型碳基固体强酸高效催化羰基化合物与二醇的缩合反应[J].科学通报,2007,52(13):1506-1508. 被引量:20
  • 8Takagaki A, Toda M, Okamura M, et al. Esterificationof higher fatty acids by a novel strong solid acid[J]. Catalysias today, 2006, 116(2):157-161. 被引量:1
  • 9Vitaly B, James H C, Jeffrey J E H, et al. Starbons: new starch-derived mesoporous carbonaceous materials with tunableproperties[J]. Angew. chem. int. ed., 2006, 45(23): 3782-3786. 被引量:1
  • 10Vitaly L B, James H C, Rafael L, et al. Versatile mesoporous carbonaceous materials for acid catalysis[J]. Chem. commun., 2007 (6):634-636. 被引量:1

二级参考文献16

  • 1Anastas P T, Kirchhoff M M. Origins, current status, and future challenges of green chemistry. Acc Chem Res, 2002, 35: 685-694 被引量:1
  • 2DeSimone J M. Practical approaches to green solvents. Science, 2002, 297(5582): 799-803 被引量:1
  • 3Harton B. Green chemistry puts down roots. Nature, 1999, 400 (19): 797-799 被引量:1
  • 4Anastas P T, Zimmermann J B. Design through the 12 principles of green engineering. Environ Sci Technol, 2003, 37: 94A-101A 被引量:1
  • 5Clark J H. Solid acids for green chemistry. Acc Chem Res, 2002, 35: 791-797 被引量:1
  • 6Misono M, Acad C R. Heterogeneous catalysis. Sci Ser Iic, 2000, 3: 471-475 被引量:1
  • 7Okuhara T. Water-tolerant solid acid catalysts. Chem Rev, 2002, 102(10): 3641-3666 被引量:1
  • 8Smith K, El-Hiti G A, Gamal A, et al. Acetylation of aromatic ethers using acetic anhydride over solid acid catalysts in a sol-vent-free system. Scope of the reaction for substituted ethers. Org Biomol Chem, 2003, 1: 1560-1564 被引量:1
  • 9Hara M, Yoshida T, Takagaki A, et al. A carbon material as a strong protonic acid. Angew Chem Int Ed, 2004, 116(22): 3015-3018 被引量:1
  • 10Toda M, Takagaki A, Okamura M, et al. Green chemistry: Bio-diesel made with sugar catalyst. Nature, 2005, 438(382): 178 被引量:1

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