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首页> 外文期刊>Energy Conversion & Management >Fuel purpose hydrocracking of biomass based Fischer-Tropsch paraffin mixtures on bifunctional catalysts
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Fuel purpose hydrocracking of biomass based Fischer-Tropsch paraffin mixtures on bifunctional catalysts

机译:基于生物量的燃料用水加氢裂化在双官能催化剂上的菌坯混合物混合物

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摘要

Two biomass-based Fischer-Tropsch paraffins comprising of 16-46 and 11-45 carbon number range alkanes were hydrocracked over zeolite mordenite and tungstated-zirconia-supported platinum catalysts. The reaction was carried out in the temperature range of 300-350 degrees C, at 40 bar pressure and hydrogen/hydrocarbon volume ratio of 600. The liquid hourly space velocity was varied in the range of 0.5 and 2.0 h(-1). The yields and the compositions of gas, gasoline, jet and gas oil fractions were studied as function of process parameters and catalyst properties. The conversion of paraffin components having more than 21 carbon atoms was determined. Under identical reaction conditions near the same conversions were obtained over the two catalysts. However, the feedstock composition significantly influenced the result of the hydrocracking process. Regularly lower conversions and higher middle distillate yields (jet + gas oil) were obtained for feedstock characterized by 11-45 carbon number range. The weaker acidic tungstated-zirconia-supported platinum catalyst was more suitable for production of engine fuels than the stronger acidic mordenite catalyst. Over platinum/tungstated-zirconia catalyst lower gas (0.5-15.0 wt%) and higher middle distillate yields (14.7-43.0 wt%) were obtained than over platinum promoted mordenite catalyst. The formation and diffusion of isoparaffins is more favored in mesopores than in micropores, therefore more isoparaffin was formed over the mesoporous tungstated-zirconia-supported platinum catalyst than over the microporous mordenite. In the micropores diffusion constraints prevailed promoting the formation of gaseous products.
机译:将包含16-46和11-45个碳数范围烷烃的两种基于生物质的Fischer-Tropsch链烷烃在沸石内硝酸酯和钨酸盐 - 氧化锆支持的铂催化剂上加氢裂化。反应在300-350℃的温度范围内进行,40巴压力和氢气/烃体积比为600.液体小时空速在0.5和2.0h(-1)的范围内变化。研究了气体,汽油,射流和瓦斯油级分的产率和组合物作为工艺参数和催化剂性能的功能。测定具有大于21个碳原子以上的石蜡组分的转化。在相同的反应条件下,在两种催化剂上获得相同的转化率。然而,原料组合物显着影响加氢裂化过程的结果。在以11-45碳数范围内的原料中获得定期降低转化率和更高的中间馏分产率(射流+汽油)。较弱的酸性钨 - 氧化锆支持的铂催化剂更适合于发动机燃料的产生,而不是较强的酸性衍射催化剂。在铂促进的Mordenite催化剂上获得铂/钨酸催化剂较低的气体(0.5-15.0wt%)和更高的中间馏分产率(14.7-43.0wt%)。异戊烷蛋白的形成和扩散在中孔中比在微孔中更赞成,因此在中孔钨酰基氧化锆支持的铂催化剂上形成更多的异戊烷,而不是微孔的丝光沸石。在微孔扩散约束普遍促进气态产物的形成。

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