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Preparation of biodiesel from waste cooking oil via two step batch catalyzed process with the aid of acid sulfuric and sodium hydroxide as the catalyst

机译:在酸性硫酸和氢氧化钠的催化下,通过两步间歇催化法从废食用油中制备生物柴油

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摘要

With environmental and energy source concerns on the rise, using agricultural fats and biological sources as fuel in diesel engines has captured increasing attention. Biodiesel has many advantages relative to petroleum. It has several processes that can be used in producing biodiesel but transesterification is the most commonly used in industry. In transesterification, it involved reaction between tryglycerides from waste cooking oil and methanol to produce biodiesel. The catalysts used in this experiment were acid sulfuric and sodium hydroxide catalyst. Two step catalyzed was chosen to be used in preparation biodiesel from waste cooking oil because the free fatty acid content was high in waste cooking oil. For the first step, the molar ratio used was 10:1 with the presence of 2 wt% of H 2SO4 as catalyst with the temperature was 95oC and 4 hours of reaction time. For the second step, the molar ratio used was 6:1 with the presence of 0.2, 0.4, 0.6, 0.8 and 1wt% of NaOH as catalyst with the temperature were 40,50,60,70, 80oC and 1 hour of reaction time. Then, the biodiesel have to analyse by titration method to check free fatty acid and acid value content. It is proved that, this method can remove both free fatty acid and acid value up to 95%. This study also has indicated that the main factors that affect the reaction are reaction temperature and catalyst concentration.
机译:随着对环境和能源问题的关注日益增加,在柴油发动机中使用农业脂肪和生物资源作为燃料已引起越来越多的关注。生物柴油相对于石油具有许多优势。它有几种可用于生产生物柴油的方法,但酯交换反应是工业上最常用的方法。在酯交换反应中,它涉及废食用油中的甘油三酸酯与甲醇之间的反应,以生产生物柴油。该实验中使用的催化剂是酸性硫酸和氢氧化钠催化剂。选择两步催化从废食用油中制备生物柴油是因为废食用油中的游离脂肪酸含量较高。第一步,使用的摩尔比为10:1,存在2 wt%的H 2 SO4作为催化剂,温度为95oC,反应时间为4小时。第二步,使用的摩尔比为6:1,存在0.2、0.4、0.6、0.8和1wt%的NaOH催化剂,温度为40、50、60、70、80°C,反应时间为1小时。然后,生物柴油必须通过滴定法进行分析,以检查游离脂肪酸和酸值含量。事实证明,该方法可以去除高达95%的游离脂肪酸和酸值。该研究还表明影响反应的主要因素是反应温度和催化剂浓度。

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    Wan Jasrina Wan Abd Ghani;

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  • 年度 2008
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