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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Hydrodechlorination of 1,2-dichloroethane and dichlorodifluoromethane over Ni/C catalysts:The effect of catalyst carbiding
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Hydrodechlorination of 1,2-dichloroethane and dichlorodifluoromethane over Ni/C catalysts:The effect of catalyst carbiding

机译:Ni / C催化剂上1,2-二氯乙烷和二氯二氟甲烷的加氢脱氯:催化剂碳化的影响

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In spite of previous reports,nickel catalysts appeared active in hydrodechlorination of 1,2-dichloroethane,producing ethylene with very high selectivity(up to 97%)at low temperatures of reaction(210-230 °C).In addition,at these temperatures,nickel deactivation by surface chloriding,observed by others,does not practically occur.The use of different nickel salts(chloride,nitrate,acetate)as catalyst precursors makes it possible to obtain different metal dispersions,reflected in variations of overall catalytic activity expressed per mass of nickel.The conditions of catalyst reduction led to a complete reduction of nickel precursor and effective removal of the counterion(Cl~-or NO_3~-).Interestingly,in the case of the chloride-and acetate-derived catalysts,the selectivity to vinyl chloride increases gradually with time on stream,at the expense of ethylene,even up to 30%.The appearance of fcc NiC_x solutions(x <= 0.1)and an hcp Ni3C phase in Ni/C catalysts used results from a massive production of ethylene,which is an efficient carbiding agent.An increasingly deeper transformation of Ni to Ni3C led to a higher selectivity to vinyl chloride.Alternatively,the Ni/C samples which were most selective toward ethylene(and characterized by a smaller Ni particle size)contained only tiny amounts of carbon in the form of NiC_x solution.The behavior of Ni/C catalysts seems to be largely regulated by the population of surface carbon species.A higher surface carbon content(implied by a higher carbon content in Ni3C than in NiC_(x<=0.1))creates an undeniable difficulty in removal of the second chlorine atom from 1,2-dichloroethane.It is suggested that,in such conditions,a new reaction route leading to vinyl chloride via a concerted elimination of HC1 is feasible.The Ni/C catalysts subjected to CC12F2 hydrodechlorination contained even higher amounts of Ni3C than the analogous samples screened in the reaction of 1,2-dichloroethane.
机译:尽管已有报道,镍催化剂在1,2-二氯乙烷的加氢脱氯中表现出活性,在低温(210-230°C)下以极高的选择性(高达97%)生产乙烯。使用其他镍盐(氯化物,硝酸盐,乙酸盐)作为催化剂前体,可以得到不同的金属分散体,这反映了总催化活性的变化。催化剂的还原条件导致镍前体完全还原并有效去除抗衡离子(Cl〜-或NO_3〜-)。有趣的是,对于氯化物和乙酸盐衍生的催化剂,其选择性氯乙烯的含量会随着生产时间的增长而逐渐增加,甚至以乙烯为代价,甚至会增加30%。fcc NiC_x溶液(x <= 0.1)的出现和所使用的Ni / C催化剂中的hcp Ni3C相是由大量产物产生Ni向Ni3C的转化越来越深,导致对氯乙烯的选择性更高。或者,Ni / C样品对乙烯的选择性最高(且Ni粒径较小) Ni / C催化剂仅含少量的NiC_x溶液形式的碳.Ni / C催化剂的行为似乎在很大程度上受表面碳物种数量的控制。较高的表面碳含量(表示Ni3C中的碳含量高于Ni3C中的碳含量)。 NiC_(x <= 0.1))在从1,2-二氯乙烷中去除第二个氯原子方面造成了不可否认的困难。建议在这种条件下,通过协同消除HCl生成氯乙烯的新反应路线是进行CC12F2加氢脱氯的Ni / C催化剂比在1,2-二氯乙烷反应中筛选的类似样品更高的Ni3C含量。

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