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Preparation of silica- and carbon-supported cobalt by electrostatic adsorption of Co(III)hexaammines

机译:通过静电吸附六亚氨基六胺制备二氧化硅和碳载钴

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摘要

Application of the simple,rational catalyst synthesis method of strong electrostatic adsorption was applied to hexaammine cobalt(III)chloride(CoHA)complexes over silica and carbon,which potentially affects the preparation of Fisher-Tropsch and other catalysts.Uptake versus pH was studied,and resulting materials were characterized by powder XRD,EXAFS,XANES,and STEM at each stage of the preparation procedure.Large differences occurred when CoHA was contacted at high pH over silica and carbon surfaces with similar points of zero charge.The Co ammine-silica interaction could be described by a purely electrostatic interaction,was very strong,and prevented reduction up to the high temperatures at which significant Co sintering occurred.However,sufficient interaction existed so that the normally lower-temperature stable hexagonal close-packing phase was retained by the metal crystallites on silica.Over carbon,CoHA underwent a reductive deammination on contact with the carbon to form large crystals of Co3O4.While this precursor phase reduces at much lower temperature than the silica-supported Co ammines,the large initial size of the Co3O4 phase also prevented the formation of small Co particles.Our findings demonstrate that high Co metal dispersion on carbon might be achieved with synthesis parameters(i.e.,other Co complexes,carbons,or impregnation conditions)that yield a highly dispersed Co precursor.
机译:将强静电吸附的简单,合理的催化剂合成方法应用于二氧化硅和碳上的六胺六氯化钴(CoHA)络合物,这可能会影响Fisher-Tropsch和其他催化剂的制备。研究了相对于pH的吸收,制备过程的每个阶段都用粉末XRD,EXAFS,XANES和STEM对所得材料进行了表征。当CoHA在高pH条件下接触具有相似零电荷点的二氧化硅和碳表面时,会有很大的差异。相互作用可以用纯静电相互作用来描述,它非常强,并且可以防止还原到发生大量Co烧结的高温。但是,由于存在足够的相互作用,所以通常低温稳定的六方密堆积相得以保留。二氧化硅上的金属微晶。在碳上,CoHA与碳接触后进行还原性脱氨基反应,形成较大的结晶虽然该前体相在比二氧化硅负载的Co胺低得多的温度下还原,但Co3O4相的较大初始尺寸也阻止了小Co颗粒的形成。我们的发现表明,高Co金属在碳上的分散性可能是通过合成参数(即其他Co络合物,碳或浸渍条件)获得的,可产生高度分散的Co前驱体。

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