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首页> 外文期刊>Journal of Catalysis >Acidic properties of sulfonic acid-functionalized FSM-16 mesoporous silica and its catalytic efficiency for acetalization of carbonyl compounds
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Acidic properties of sulfonic acid-functionalized FSM-16 mesoporous silica and its catalytic efficiency for acetalization of carbonyl compounds

机译:磺酸官能化的FSM-16介孔二氧化硅的酸性及其对羰基化合物缩醛化的催化效率

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Propyl-sulfonic acid-functionalized FSM-16 mesoporous silica (SO3H-FSM) is prepared by a conventional post-modification method. For the acetalization of carbonyl compounds with ethylene glycol, SO3H-FSM shows a higher rate and 1,3-dioxolane yield than conventional heterogeneous solid acids such as zeolites, montmorillonite K10 clay, silica-alumina, and the sulfonic resin. SO3H-FSM is stable during the reaction, with no leaching and deactivation of sulfonic acid groups, and is reusable without loss of its activity. The acidity and hydrophilicity of SO3H-FSM are well characterized by the microcalorimetry of NH3 adsorption, NH3-TPD, and H2O-TPD, and the result is compared with those for various aluminosilicate zeolites (HZSM5, HBEA, HY) and K10 clay. It is found that NH3-TPD is not suitable for characterizing the acidity of SO3H-FSM, because the decomposition of SO3H groups on SO3H-FSM begins above 200 degrees C. An NH3 adsorption microcalorimetric experiment at 150 degrees C shows that, compared with HZSM5, SO3H-FSM has a smaller number of acid sites but has a similar number of strong acid sites with ammonia adsorption heat above 140 kJ mol(-1). Comparison of the structural properties and catalytic results shows that a large pore diameter and low hydrophilicity are required to obtain high activity. Bronsted acid sites with a relatively strong acid strength are more suitable for this reaction, but the high acid concentration is not indispensable. The high activity of SO3H-FSM should be caused by the presence of the strong Bronsted acid sites in the mesopore with a relatively low hydrophilicity, where both reactants can smoothly access the acid sites. (c) 2005 Elsevier Inc. All rights reserved.
机译:丙磺酸官能化的FSM-16介孔二氧化硅(SO3H-FSM)通过常规的后改性方法制备。对于用乙二醇进行羰基化合物的缩醛化反应,SO3H-FSM与常规的非均相固体酸(如沸石,蒙脱土K10粘土,二氧化硅-氧化铝和磺酸树脂)相比,具有更高的产率和1,3-二氧戊环产率。 SO 3 H-FSM在反应期间是稳定的,没有磺酸基团的浸出和失活,并且可以重复使用而不会损失其活性。 SO3H-FSM的酸度和亲水性通过NH3吸附,NH3-TPD和H2O-TPD的量热法进行了很好的表征,并将结果与​​各种铝硅酸盐沸石(HZSM5,HBEA,HY)和K10粘土的结果进行了比较。发现NH3-TPD不适合表征SO3H-FSM的酸度,因为SO3H-FSM上的SO3H基团的分解开始于200摄氏度以上。150摄氏度的NH3吸附微量量热实验表明,与HZSM5相比,SO3H-FSM具有较少的酸性位,但具有相似数量的强酸性位,且氨吸附热高于140 kJ mol(-1)。结构性能和催化结果的比较表明,要获得高活性需要大孔径和低亲水性。具有相对强的酸强度的布朗斯台德酸位点更适合该反应,但是高酸浓度不是必不可少的。 SO3H-FSM的高活性应归因于介孔中强布朗斯台德酸位点的存在,该位点具有相对较低的亲水性,这两种反应物都能顺利进入酸位点。 (c)2005 Elsevier Inc.保留所有权利。

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