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Acetylation of glycerol using MgO-CaO catalysts with different CaO loadings

机译:使用不同CaO载荷的MgO-CaO催化剂甘油的乙酰化

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The synthesis of three catalytic samples of MgO-CaO containing 20, 30, 50 wt% of CaO was carried out by a co-precipitation method. Also pure MgO and CaO were prepared. Infrared spectroscopy, Raman, X-ray photoelectron, X-ray diffraction, atomic force microscopy and Temperature-Programmed Desorption of CO2 characterized powder samples. Those analyses permitted to differentiate phases in mixed oxides in catalysts and to identify phases that gave a basic character to solid samples. The powders were used to catalyze the acetylation of glycerol to produce mono, di and triacetin at 70 degrees C during 280 min. The reaction products were followed by IR, and gas chromatograph analysis. The highest glycerol conversion (89%) was attained by using 50MgO-50CaO catalytic sample, while pure MgO exhibited the poorest conversion (of c.a. 64%). Regarding selectivity toward triacetin, the catalyst containing 50 wt% CaO was the best, reaching a value of 92%, while yielding the lowest diacetin and monoacetin (0.5 and 5%, respectively). Despite the catalyst types, triacetin selectivity profiles showed increased as reaction time did, whereas diacetin underwent a continuous decrease and monoacetin remained almost constant with the reaction time. The study results demonstrated that MgO-CaO mixed oxides provided a synergetic effect in glycerol acetylation in terms of both conversion and selectivity to valuable products.
机译:通过共沉淀法进行含有20,30,50wt%的MgO-CaO的三种催化样品的合成。还制备了纯MgO和CaO。红外光谱,拉曼,X射线光电子,X射线衍射,原子力显微镜和CO 2表征粉末样品的温度编程解吸。允许这些分析允许在催化剂中的混合氧化物中分化相位并鉴定给予固体样品的基本特征的相位。粉末用于催化甘油的乙酰化,在280分钟期间在70℃下在70℃下生产单甘油。反应产物之后是IR,以及气相色谱分析。通过使用50MgO-50CaO催化样品获得最高甘油转化率(89%),而纯MgO表现出最贫差的转化率(C.a.64%)。关于三循环素的选择性,含有50wt%CaO的催化剂是最好的,达到92%的值,同时产生最低的糖尿病和单乙酸(分别为0.5和5%)。尽管催化剂类型,但是随着反应时间的情况表明,三乙酸酯选择性谱表现出增加,而糖尿肽经历连续减少,并且单乙酸几乎恒定,反应时间几乎恒定。研究结果表明,在转化和选择性对有价值的产品方面,MgO-CaO混合氧化物在甘油乙酰化方面提供了协同作用。

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