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An efficient process to synthesize solketal from glycerol over tin (Ⅱ) silicotungstate catalyst

机译:从锡(Ⅱ)硅钨酸盐催化剂上用甘油合成甲基芳基的有效方法

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摘要

In this work, Sn(II)-exchanged silicotungstic acid salt (i.e., Sn2SiW12O40) was synthesized and evaluated as the catalyst on the acetalization of glycerol with acetone to produce solketal, a versatile bioadditive of fuel. The Sn2SiW12O40 salt was compared to the other solid Keggin heteropoly salts (i.e., Sn3/4PMo12O40, Sn3/4PW12O40), and liquid (i.e., HCl, H2SO4 and p-toluenesulfonic acid) catalysts. Amongst the catalysts assessed, it was the most active, achieving a high conversion (ca. 99%, after 1 h reaction at room temperature) and selective (ca. 97%) toward the formation of solketal. Moreover, the Sn(2)SiW(12)O(40 )salt demonstrated to be more active than acid and precursor Tin (II) chloride salt, as well as other heteropoly salts and solid supported catalysts. The effects of the main reaction variables were assessed. The Sn(II) cation, as well as the silicotungstate anion, showed being essential to convert glycerol to solketal. Insights on the reaction mechanism were performed. In a simple recycle procedure, the solketal was purified, the acetone excess recycled, and the catalyst was reused without loss activity.
机译:在这项工作中,Sn(II)-Exchanged硅钨酸盐(即,SN2SIW12O40)被合成并作为催化剂作为丙酮制备甲基酮的甘油的致丙酮,以产生甲基酮,这是燃料的多功能生物粘合剂。将SN2SIW12O40盐与其他固体Keggin杂多盐(即,SN3 / 4PMO12O40,SN3 / 4PW12O40)和液体(即HCl,H 2 SO 4和对甲苯磺酸)催化剂进行比较。在评估的催化剂中,它是最活跃的,最活跃的,在室温下的1小时后,在1小时内达到高转化率(CA> 99%),并选择性(约97%)朝向形成雄蛋白。此外,SN(2)SiW(12)O(40)溶解的盐比酸和前体锡(II)氯化物盐,以及其他杂多盐和固体负载型催化剂更活跃。评估主要反应变量的效果。 Sn(II)阳离子以及硅钨酸盐阴离子表现为将甘油转化为Solketal的必需品。进行了对反应机制的见解。在简单的再循环过程中,纯化甲基酮,丙酮过量再循环,催化剂重复使用而不会损失活性。

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