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首页> 外文期刊>Fuel >Production of jet fuel by hydrorefining of Fischer-Tropsch wax over Pt/Al-TUD-1 bifunctional catalyst
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Production of jet fuel by hydrorefining of Fischer-Tropsch wax over Pt/Al-TUD-1 bifunctional catalyst

机译:通过PT / Al-Tud-1双功能催化剂的Fischer-Tropsch蜡加氢生产喷射燃料

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摘要

TUD-1 supported bifunctional platinum catalysts were prepared and characterized for structural and textural properties, acidity, and platinum dispersion. The acidity of TUD-1 was varied by isomorphous substitution of Al and Ti in the framework. The TUD-1 supports possess a three-dimensional amorphous structure as shown by XRD. BET-N2 adsorption and pyridine FTIR studies revealed that the incorporation of Al in the TUD-1 framework enhances the surface area and generates Bronsted acidity. The catalysts were screened for hydrorefining of Fischer-Tropsch wax with C8-C44 n-paraffins. The catalysts prepared with Si-TUD-1 and Ti-TUD-1 supports were not active for hydrocracking and hydroisomerization due to the absence of Bronsted acid sites, which was verified by pyridine FTIR. Increasing the amount of Al in the framework gradually increased the Bronsted acid sites and thus promoted hydrocracking and hydroisomerization of F-T wax. Pt/Al-TUD-1 catalyst with a Si/Al ratio of 10 produced more jet fuel range hydrocarbons. Hydrorefining of F-T wax was evaluated over an optimal Pt/Al-TUD-1 (Si/Al = 10) catalyst at different pressures and temperatures. Hydroisomerization was favored at low hydrogen pressure. Increasing the temperature shifted the hydrocarbon distribution more towards gasoline due to severe cracking. The temperature of 330 degrees C and a hydrogen pressure of 5 MPa were found to be optimum to produce jet fuel range hydrocarbons that meet the ASTM specification of cold flow properties. This study proves the feasibility of the production of renewable jet fuel that is directly compatible with fossil-based aviation engines, through hydrorefining of F-T waxes using a mesoporous bifunctional catalyst.
机译:制备Tud-1支持的双官能铂催化剂,其特征在于结构和纹理性质,酸度和铂分散体。通过框架中的Al和Ti的同构替代而改变Tud-1的酸度。 TUD-1支撑件具有三维非晶结构,如XRD所示。 Bet-N2吸附和吡啶FTIR研究表明,在TUD-1框架中的掺入增强了表面积并产生了抗正囊酸度。筛选催化剂用C8-C44 N-链烷烃筛选用于加氢的Fischer-Tropsch蜡。由于不存在通过吡啶FTIR验证,用Si-Tud-1和Ti-Tud-1支撑件制备的催化剂未活性加氢裂化和加氢异构化。增加框架中的Al的量逐渐增加了伪造酸部位,从而促进了F-T蜡的加氢裂化和加氢异构化。具有Si / Al比例的Pt / Al-Tud-1催化剂,其10产生的喷射燃料放射线烃。在不同压力和温度下在最佳Pt / Al-Tud-1(Si / Al = 10)催化剂上评价F-T蜡的水合。氢异构化在低氢气压力下受到青睐。由于严重的裂缝,增加温度将烃分布移向汽油。发现330℃和5MPa的氢气压力的温度是最佳的,以产生满足冷流性能的ASTM规范的射流燃料放射线烃。本研究证明了通过使用介孔双官能催化剂的F-T蜡的加氢,可再生射流燃料生产直接与化石的航空发动机的可行性。

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