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Easily recoverable titanosilicate zeolite beads with hierarchical porosity: Preparation and application as oxidation catalysts

机译:具有分级孔隙率的易于回收的钛硅酸盐沸石珠:制备和用作氧化催化剂

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摘要

Titanosilicate zeolite beads with hierarchical porosity and 0.2-0.5 mm diameter (HPB-TS-1) have been synthesized from a titanosilicate solution, employing a porous anion-exchange resin as shape- and structure-directing template. The characterization results showed the existence of crystalline TS-1 nanoparticles and of a network of connected large meso/macropores in the interior of the beads. These bead materials are active and selective heterogeneous catalysts for two classes of industrially relevant oxidation reactions: the hydroxylation of phenol and the epoxidation of alkenes. In both cases, a green oxidant such as hydrogen peroxide was utilized. HPB-TS-1 beads displayed high activity in the hydroxylation of phenol, due to their crystalline TS-1 structure with isolated tetrahedral Ti species. In the epoxidation of cyclohexene, HPB-TS-1 gave conversion comparable to that over a benchmark catalyst such as Ti-MCM-41, but more than double yield and selectivity of the target product, cyclohexene oxide. HPB-TS-1 was also active and selective in the epoxidation of other bulky alkenes, i.e., cis-cyclooctene and trans, trans, cis-1,5,9-cyclododecatriene. The catalytic performance of HPB-TS-1 stems from the presence of crystalline TS-1 nanodomains, which are accessible through a network of mesoimacropores within the beads. Notably, the bead format of these catalysts causes their spontaneous settling upon cessation of the agitation, thus enabling their straightforward separation from the reaction mixture. The HPB-TS-1 catalysts could be efficiently recycled in the hydroxylation of phenol with aqueous H2O2 via a calcination approach. (C) 2015 Elsevier Inc. All rights reserved.
机译:使用多孔阴离子交换树脂作为形状和结构导向模板,从钛硅酸盐溶液合成了具有分级孔隙度和直径为0.2-0.5 mm的钛硅酸盐沸石珠(HPB-TS-1)。表征结果表明,在珠粒内部存在结晶的TS-1纳米颗粒和相连的大介孔/大孔网络。这些珠粒材料是用于两类与工业相关的氧化反应的活性和选择性多相催化剂:苯酚的羟基化和烯烃的环氧化。在两种情况下,都使用绿色氧化剂,例如过氧化氢。 HPB-TS-1磁珠由于具有分离的四面体Ti物种的TS-1晶体结构,因此在酚的羟基化中显示出高活性。在环己烯的环氧化中,HPB-TS-1的转化率可与基准催化剂(如Ti-MCM-41)相比,但目标产物环己烯氧化物的收率和选择性提高了一倍以上。 HPB-TS-1在其他大体积烯烃即顺式-环辛烯和反式,反式,顺式,1,5,9-环十二碳三烯的环氧化中也具有活性和选择性。 HPB-TS-1的催化性能源于结晶TS-1纳米域的存在,可通过珠粒内的中大孔网络访问这些晶体。值得注意的是,这些催化剂的珠粒形式在停止搅拌时导致其自发沉降,因此使得它们能够直接从反应混合物中分离。 HPB-TS-1催化剂可通过煅烧方法有效地循环利用苯酚与过氧化氢水溶液进行羟基化反应。 (C)2015 Elsevier Inc.保留所有权利。

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