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Selectivity As A Function Of Nanoparticle Size In The Catalytic Hydrogenation Of Unsaturated Alcohols

机译:在不饱和醇催化加氢中,选择性与纳米粒径的关系

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Layer-by-layer adsorption of poly(acrylic acid)-Pd(ll) complexes and poly(ethylenimine) on alumina powder followed by reduction of Pd(ll) with NaBH_4 yields Pd-nanoparticle catalysts embedded in multilayer polyelectrolyte films. The use of different ratios of poly(acrylic acid) to Pd(ll) in deposition solutions gives a series of films with Pd nanoparticles whose average diameters range from 2.2 to 3.4 nm, and the catalytic selectivities of these nanoparticles vary dramatically with their size. Turnover frequencies (TOFs) for the hydrogenation of monosubstituted unsaturated alcohols increase with decreasing average nanoparticle size, whereas multisubstituted unsaturated alcohols show the opposite trend. Hence, the ratio of TOFs for the hydrogenation of allyl alcohol and crotyl alcohol is 39 with average particle diameters of 2.2 nm and only 1.3 with average particle diameters of 3.4 nm. Ratios of TOFs for hydrogenation of allyl alcohol and β-methallyl alcohol are as high as 240 with the smallest nanoparticles, but substantial isomerization of β-methallyl alcohol complicates this comparison. Increasing selectivity with decreasing average particle size occurs with both films deposited on alumina powder and nanoparticles stabilized by polyelectrolytes in solution. Presumably, high selectivities occur on the smallest nanoparticles because the active sites on the smallest Pd nanoparticles are less available for binding and hydrogenation of multisubstituted double bonds than are active sites on larger particles.
机译:聚(丙烯酸)-Pd(II)配合物和聚(乙烯亚胺)在氧化铝粉末上的逐层吸附,然后用NaBH_4还原Pd(II),得到嵌入多层聚电解质薄膜中的Pd-纳米颗粒催化剂。在沉积溶液中使用不同比例的聚丙烯酸与Pd(II)可以得到一系列具有Pd纳米粒子的薄膜,其平均直径范围为2.2至3.4 nm,并且这些纳米粒子的催化选择性随其尺寸而变化很大。单取代不饱和醇氢化的周转频率(TOFs)随着平均纳米颗粒尺寸的减小而增加,而多取代不饱和醇则呈现相反的趋势。因此,用于烯丙醇和巴豆醇的氢化的TOFs的比率为39,平均粒径为2.2nm,而只有1.3,平均粒径为3.4nm。用最小的纳米颗粒,烯丙醇和β-甲基烯丙醇的氢化TOFs高达240,但是β-甲基烯丙醇的大量异构化使这一比较复杂化。沉积在氧化铝粉末上的膜和通过溶液中的聚电解质稳定的纳米颗粒都会发生选择性的提高和平均粒径的减小。据推测,在最小的纳米颗粒上会发生高选择性,因为最小的Pd纳米颗粒上的活性位比大颗粒上的活性位更不易用于多取代双键的键合和氢化。

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