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首页> 外文期刊>Fuel Processing Technology >Liquid fuel production from syngas using bifunctional CuO-CoO-Cr2O3 catalyst mixed with MFI zeolite
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Liquid fuel production from syngas using bifunctional CuO-CoO-Cr2O3 catalyst mixed with MFI zeolite

机译:使用双功能CuO-CoO-Cr2O3催化剂与MFI沸石混合从合成气生产液体燃料

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摘要

CuO-CoO-Cr2O3 mixed with MFI Zeolite (Si/Al = 35) prepared by co-precipitation was used for synthesis gas conversion to long chain hydrocarbon fuel. CuO-CoO-Cr2O3 catalyst was prepared by co-precipitation method using citric acid as complexant with physicochemical characterization by BET, TPR, TGA, XRD, H2-chemisorptions, SEM and TEM techniques. The conversion experiments were carried out in a fixed bed reactor, with different temperatures (225-325 ℃), gas hourly space velocity (457 to 850 h~(-1)) and pressure (28-38 atm). The key products of the reaction were analyzed by gas chromatography mass spectroscopy (GC-MS). Significantly high yields of liquid aromatic hydrocarbon products were obtained over this catalyst. Higher temperature and pressure favored the CO conversion and formation of these liquid (C5-C_(15)) hydrocarbons. Higher selectivity of C5 + hydrocarbons observed at lower H2/CO ratio and GHSV of the feed gas. On the other hand high yields of methane resulted, with a decrease in C5+ to C_(11) +- fractions at lower GHSV. Addition of MFI Zeolite (Si/Al = 35) to catalyst CuO-CoO-Cr2O3 resulted a high conversion of CO-hydrogenation, which may be due to its large surface area and small particle size creating more active sites. The homogeneity of various components was also helpful to enhance the synergistic effect of Co promoters.
机译:与共沉淀制备的MFI沸石(Si / Al = 35)混合的CuO-CoO-Cr2O3用于将合成气转化为长链烃类燃料。以柠檬酸为络合物,通过共沉淀法制备了CuO-CoO-Cr2O3催化剂,并通过BET,TPR,TGA,XRD,H2-化学吸附,SEM和TEM等方法对其进行了理化表征。转化实验在固定床反应器中进行,温度,温度(225-325℃),气体时空速(457至850 h〜(-1))和压力(28-38 atm)不同。通过气相色谱质谱法(GC-MS)分析反应的关键产物。在该催化剂上获得了高产率的液态芳烃产物。较高的温度和压力有利于这些液体(C5-C_(15))烃的CO转化和形成。在进料气的较低H2 / CO比和GHSV下观察到较高的C5 +烃选择性。另一方面,产生了高产率的甲烷,在较低的GHSV下,C5 +含量降低至C_(11)+-馏分。在催化剂CuO-CoO-Cr2O3中添加MFI沸石(Si / Al = 35)导致CO加氢转化率高,这可能是由于其大表面积和小粒径产生了更多的活性位。各种组分的均质性也有助于增强Co启动子的协同作用。

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