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    磷化物催化剂体系下二苯并噻吩加氢反应网络研究

    Study on the network of dibenzothiophene hydrogenation using phosphide catalyst

    • 摘要: 为考察二苯并噻吩在磷化物体系下催化加氢的反应网络,以分子筛SBA-15为空白载体,利用等体积浸渍制取了一系列磷化物催化剂,Ni/P摩尔比为1.25,对不同Ni金属担载量的磷化物催化剂的性质进行了分析。采用含有1%二苯并噻吩的模型化合物为原料进行加氢脱硫试验,利用20 m L连续固定床加氢精制装置对制备的磷化物催化剂进行了活性评价。结果表明,相对于商业催化剂,低温和磷化物催化剂体系下二苯并噻吩具有更高的转化率,280℃转化率可达80%以上;碱性氮化物喹啉的存在抑制了二苯并噻吩加氢反应,转化率在320℃时由接近100%降至70%左右,此条件下,产物中联苯以及环己烷基苯的选择性随温度变化不大,二苯并噻吩大部分通过直接脱硫路径进行转化。评价结果显示,磷化物催化剂具有更高的氢解活性和更好的直接加氢脱硫效果。

       

      Abstract: In order to research the network of dibenzothiophene hydrogenation using phosphide catalyst,molecular sieve SBA-15 was used as the supporter to prepare the nickel phosphide catalyst by incipient impregnation method. The Ni/P mole ratio was 1. 25,and catalysts with different loading of nickel phosphide were characterized. Model compound dibenzothiophene with 1% concentration was used to conduct the hydrogenation experiment,the phosphide catalyst was evaluated on a 20 m L fixed bed hydrogenation equipment.The results show that compared with the ordinary commercial catalyst,phosphide catalysts have a higher conversion rate on diben zothiophene at low temperature,which could reach more than 80% at 280 ℃. The existence of quinoline presents a strong inhibitory effect on the hydrogenation of dibenzothiophene,and thus the conversion rate is reduced from 100% to 70% at 320 ℃.The selectivity of biphenyl and cyclohexylbenzene are very small,and the transformation of dibenzothiophene is almost entirely via the direct desulfurization pathway. The phosphide catalyst has higher hydrogenolysis capacity and better direct desulfurization selectivity.

       

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