National Biofuels Energy Laboratory, Next Energy, Wayne State University, USA.
Bioresour Technol. 2010 Jun;101(12):4409-14. doi: 10.1016/j.biortech.2010.01.099. Epub 2010 Feb 11.
Methylesters and ethylesters of fatty acids were synthesized using homogeneous CH(3)ONa and CH(3)CH(2)ONa, anion exchanged resin, and CaO-La(2)O(3) catalysts. Methanol, ethanol, and methanol/ethanol mixtures were used as the alcohol feed for transesterification of soybean oil. With a homogeneous catalyst (CH(3)ONa) there was essentially no difference in conversion rates between methanolysis and ethanolysis in batch reactions. However, with a heterogeneous resin and CaO-La(2)O(3) catalysts, significant differences in the conversion rates between the methanolysis and ethanolysis were observed. The formation rate of methylesters over a CaO-La(2)O(3) catalyst was higher than that of ethylesters, which may be attributable to a steric hindrance effect. Conversely, with a heterogeneous resin catalyst, the conversion rate of ethylester was higher than that of methylesters which may be attributable to the surface hydrophobicity of the anion exchanged resin. When the transesterification of soybean oil was carried out with an equimolar methanol/ethanol mixture, the yield ratio of methylester to ethylester formed within the first 30 min was 2.6 for the homogeneous catalyst (0.3% CH(3)ONa), and 3.4 for the heterogeneous CaO-La(2)O(3)catalyst. These differences in selectivity are likely due to both the higher reactivity of methoxide and to a steric hindrance effect of ethoxide on the catalyst surface. In addition, the transformation of methylester to ethylester was observed when a methanol/ethanol mixture was used.
脂肪酸的甲酯和乙酯是使用均相的 CH(3)ONa 和 CH(3)CH(2)ONa、阴离子交换树脂和 CaO-La(2)O(3)催化剂合成的。甲醇、乙醇和甲醇/乙醇混合物被用作大豆油酯交换的醇进料。在间歇反应中,使用均相催化剂(CH(3)ONa)时,甲醇解和乙醇解的转化率基本没有差异。然而,使用非均相树脂和 CaO-La(2)O(3)催化剂时,甲醇解和乙醇解的转化率存在显著差异。在 CaO-La(2)O(3)催化剂上,甲酯的形成速率高于乙酯,这可能归因于空间位阻效应。相反,在非均相树脂催化剂上,乙酯的转化率高于甲酯,这可能归因于阴离子交换树脂的表面疏水性。当使用等摩尔甲醇/乙醇混合物进行大豆油的酯交换时,在最初 30 分钟内形成的甲酯与乙酯的产率比在均相催化剂(0.3% CH(3)ONa)下为 2.6,在非均相 CaO-La(2)O(3)催化剂下为 3.4。这种选择性的差异可能是由于甲氧基的更高反应性以及乙氧基在催化剂表面的空间位阻效应。此外,当使用甲醇/乙醇混合物时,观察到甲酯向乙酯的转化。