共查询到19条相似文献,搜索用时 62 毫秒
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《应用化工》2022,(3):532-536
以丙烯酸甲酯为改性剂,对氧化钙表面进行改性,研究丙烯酸甲酯改性氧化钙催化油脂-甲醇酯交换体系制备生物柴油性能的影响。考察了改性剂用量、醇油摩尔比以及催化剂用量对体系酯化率的影响,并对催化剂进行表征。结果表明,表面改性后,氧化钙的催化性能得到极大改善。在反应温度为65℃、丙烯酸甲酯改性剂用量为0.5%、醇油摩尔比为20∶1、催化剂用量为15%、反应时间2 h条件下,生物柴油产率高达96.55%,与未改性氧化钙相比,相同条件下生物柴油产率提高16.18%。同时,丙烯酸甲酯改性氧化钙还具有良好的耐水性能,在体系含水量1%条件下催化制备生物柴油产率仍能达到81%。催化剂BET表征结果显示,改性后氧化钙较改性前的比表面积、平均孔径和孔体积均增大;热重表征结果表明,氧化钙改性后热稳定性提高,颗粒分散性增强;XRD、FTIR表征显示,丙烯酸甲酯改性剂已经成功键合到氧化钙表面。 相似文献
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疏水改性氧化钙催化制备生物柴油的研究 总被引:1,自引:0,他引:1
以溴化苄作为改性剂,采用化学键合方法对市售氧化钙进行表面改性,考察改性氧化钙固体碱催化菜籽油-甲醇酯交换反应制备生物柴油的性能,并在此基础上对该催化体系的耐水性进行考察。通过对反应体系中醇/油摩尔比、催化剂用量和反应时间进行优化,最终得出在醇/油摩尔比为15∶1,催化剂用量为5%以及表面改性剂溴化苄用量为0.2%时,表面改性氧化钙上生物柴油产率在反应3h即可达到99.8%,而未改性氧化钙为催化剂时在相同反应条件下生物柴油产率仅为35.3%。 相似文献
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以SO42-/ZrO2为母体,引入稀土元素La、Ce对其进行改性,制备出一系列稀土固体超强酸催化剂,用X射线衍射、红外光谱和BET手段表征了催化剂的物化性能。研究了催化剂合成生物柴油的催化性能,系统考察了n(甲醇):n(脂肪酸甘油三酯)、催化剂用量、反应温度、反应时间等因素对生物柴油产率的影响。结果表明:稀土的引入使活性四方相ZrO2更加稳定;催化剂中形成了固体超强酸结构,且改性后酸强度增大,催化剂活性中心数目增加。SO42-/ZrO2-La2O3的催化活性较高,n(甲醇)∶n(脂肪酸甘油三酯)=10∶1、m(催化剂)∶m(原料油)=4∶100、反应温度250℃、反应时间9 h,此时甲酯的产率可达到73.46%。该催化剂活性较高,重复使用3次后生物柴油产率仍在60%之上。 相似文献
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NaF/CaO固体碱催化制备生物柴油 总被引:2,自引:0,他引:2
采用等体积浸渍法制备了NaF/CaO催化剂,用于催化大豆油与甲醇酯交换反应制备生物柴油。考察了催化剂制备条件和反应条件对酯交换反应的影响。结果表明,通过等体积浸渍法、500℃焙烧4h和NaF与CaO的质量比6:1制得的催化剂,在70℃、催化剂用量为油质量的8%、醇油物质的量比9:1和反应2 h条件下,生物柴油收率可达95%。与单纯的CaO相比,NaF/CaO催化剂的催化活性明显提高。用共聚焦拉曼光谱考察了催化剂的表面特征。 相似文献
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分子筛微波辐射负载CaO催化合成生物柴油 总被引:2,自引:0,他引:2
研究微波辐射法制备固体碱催化剂CaO/NaY在合成生物柴油中的应用。结果表明,该催化剂在醇油摩尔比9∶1,催化剂质量分数3%,反应温度65℃,反应时间3 h等条件下,以精制大豆油为原料制备的生物柴油得率可达95%;而以酸值(以KOH计)为4 mg/g和含水质量分数为1.5%的油脂为原料,生物柴油得率可分别达到92.4%和84.8%。催化剂结构表征表明:微波辐射改善了CaO在载体NaY上的分散,其总碱量(H-27)达到3.798mmol/g,是一种固体超强碱。 相似文献
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用氢氧化钙和氢氧化钠联合改性活性白土制备了膨润土固体碱催化剂,并用于麻疯树油和甲醇酯交换反应合成生物柴油。主要目的是研究酯交换反应的动力学及纯化反应获得的粗生物柴油使其达到相关国际标准。首先在消除内外扩散的条件下,测定323.15~338.15 K温度范围内的反应动力学数据,并用拟均相模型进行拟合。在室温下使用膨润土为吸附剂对粗生物柴油进行纯化,以移除游离甘油为目标,考察吸附剂用量和吸附时间的影响,以获得适宜纯化条件。结果表明,膨润土固体碱催化剂有较高的活性和稳定性,所得生物柴油粗产品质量较好;反应过程符合拟一级反应动力学机理,活化能67.87 kJ·mol-1;在3%(质量分数)的膨润土用量,室温吸附30 min的条件下,纯化后的生物柴油符合欧洲标准(EN 14214)且产品收率超过96%。 相似文献
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La/zeolite beta was prepared by an ion exchange method and used to synthesize the biodiesel (fatty acid methyl esters, FAME). The La(NO3)3 was applied as the ion exchange precursor to incorporate La ion into zeolite beta. The composition of the zeolite beta before and after ion exchange was analyzed by the SEM microphotographs and EDS spectrograms, the Brønsted and Lewis acid sites were investigated by FTIR imaging. The transesterification was carried out in a batch reactor and the composition of the FAME product was determined by a potassium hydroxide saponification method. The syntheses conditions with respect to catalytic activities have been optimized individually. Results of the experiment showed that La/zeolite beta shows higher conversion and stability than zeolite beta for the production of biodiesel, which may be correlated to the higher quantity of external Brønsted acid sites available for the reactants. The product consists of a mixture of monoalkyl esters primarily, and when the methanol/ soybean oil molar ratio was 14.5, reaction temperature at 333 K, reaction time 4 h and catalyst/soybean oil mass ratio of 0.011, the conversion of triglyceride 48.9 wt% was obtained from this optimal reaction condition. 相似文献
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Yun Liu Yunjun Yan Fang Hu An'na Yao Zhicheng Wang Fuxiang Wei 《American Institute of Chemical Engineers》2010,56(6):1659-1665
Preparation of biodiesel from waste cooking oil catalyzed by combined lipases in tert‐butanol medium was investigated. Several crucial parameters affecting biodiesel yield were optimized by response surface methodology, such as dosage of combined lipases of Novozym 435 and Lipozyme TLIM, weight ratio of Novozym 435 to Lipozyme TLIM, amount of tert‐butanol, reaction temperature, and molar ratio of oil to methanol. Under the optimized conditions, the highest biodiesel yield was up to 83.5% The proposed model on biodiesel yield had a satisfactory coefficient of R2 (= 94.02%), and was experimentally verified. The combined lipases exhibited high‐operational stability. After 30 cycles (300 h) successively, the activity of combined lipases maintained 85% of its original activity. A reaction kinetic model was proposed to describe the system and deduced to be a pseudo‐first‐order reaction, and the calculated activation energy was 51.71 kJ/mol. © 2009 American Institute of Chemical Engineers AIChE J, 2010 相似文献
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《Catalysis communications》2008,9(12):2159-2165
La/zeolite beta was prepared by an ion exchange method and used to synthesize the biodiesel (fatty acid methyl esters, FAME). The La(NO3)3 was applied as the ion exchange precursor to incorporate La ion into zeolite beta. The composition of the zeolite beta before and after ion exchange was analyzed by the SEM microphotographs and EDS spectrograms, the Brønsted and Lewis acid sites were investigated by FTIR imaging. The transesterification was carried out in a batch reactor and the composition of the FAME product was determined by a potassium hydroxide saponification method. The syntheses conditions with respect to catalytic activities have been optimized individually. Results of the experiment showed that La/zeolite beta shows higher conversion and stability than zeolite beta for the production of biodiesel, which may be correlated to the higher quantity of external Brønsted acid sites available for the reactants. The product consists of a mixture of monoalkyl esters primarily, and when the methanol/ soybean oil molar ratio was 14.5, reaction temperature at 333 K, reaction time 4 h and catalyst/soybean oil mass ratio of 0.011, the conversion of triglyceride 48.9 wt% was obtained from this optimal reaction condition. 相似文献