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首页> 外文期刊>Fuel >A route to produce renewable diesel from algae: Synthesis and characterization of biodiesel via in situ transesterification of Chlorella alga and its catalytic deoxygenation to renewable diesel
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A route to produce renewable diesel from algae: Synthesis and characterization of biodiesel via in situ transesterification of Chlorella alga and its catalytic deoxygenation to renewable diesel

机译:一种从藻类生产可再生柴油的途径:通过小球藻藻的原位酯交换反应及其催化脱氧制得可再生柴油的生物柴油的合成和表征

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In situ transesterification of Chlorella alga was performed using 5-20 wt% sulfuric acid as a catalyst at either 60 or 100 degrees C. The maximum ester yield in the range of 96-98% is comparative to the specification of ester content in biodiesel, 96%. A high excess of methanol was used in transesterification ensured also a high ester yield. The FAME was purified via adsorption of chlorophyll and carotenoids onto a clay. Properties of the purified biodiesel were investigated with several methods. The results showed that the Chlorella based biodiesel exhibits slightly lower oxidative and thermal stability compared to soybean based biodiesel due to the presence of polyunsaturated FAMEs. In addition to biodiesel, also the residual biomass was characterized showing that it contained sugars and proteins. An additional hydrogenation would increase the oxidative stability. Hydrodeoxygenation of Chlorella based biodiesel was also demonstrated over 5 wt% Ni-HY-80 zeolite with SiO2/Al2O3 ratio of 80 and with 5 wt% Pd/C at 300 degrees C and 30 bar in dodecane as a solvent. Ni-HY-80 was superior to Pd/C catalyst giving more than 95% yield of hydrocarbons. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在60或100摄氏度下,使用5-20 wt%的硫酸作为催化剂进行小球藻藻的原位酯交换反应。最大酯收率在96-98%的范围内与生物柴油中酯含量的规定相比, 96%。在酯交换反应中使用大量过量的甲醇,这也确保了较高的酯收率。通过将叶绿素和类胡萝卜素吸附到粘土上来纯化FAME。用几种方法研究了纯化的生物柴油的性质。结果表明,由于存在多不饱和FAME,与基于大豆的生物柴油相比,基于绿藻的生物柴油显示出稍低的氧化和热稳定性。除生物柴油外,还对残留生物质进行了表征,表明其含有糖和蛋白质。额外的氢化将增加氧化稳定性。还证实了小球藻基生物柴油的加氢脱氧反应是在5%的SiO2 / Al2O3比为80的Ni-HY-80沸石中,在300℃和30 bar的十二烷中作为溶剂,使用5 wt%的Pd / C。 Ni-HY-80优于Pd / C催化剂,烃产率超过95%。 (C)2015 Elsevier Ltd.保留所有权利。

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