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Benzene, toluene and xylene (BTX) from in-situ gas phase hydrodeoxygenation of guaiacol with liquid hydrogen donor over bifunctional non-noble-metal zeolite catalysts

机译:在双功能非贵金属沸石催化剂上用液态氢给体对愈创木酚进行气相加氢脱氧加氢的原位苯,甲苯和二甲苯(BTX)

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Hydrogen donors were employed to replace pure hydrogen as a hydrogen source for in-situ gas phase HDO due to their low storage and transportation cost. A series of catalysts have been prepared by modifying the zeolite HZSM-5 with polymetallic and multi-carriers. Gas-phase hydrodeoxygenation (HDO) of guaiacol was conducted under a pressure 2 MPa and a temperature at 350 degrees C. The effect of polymetallic and multi-carrier modification on HDO activity was investigated. The physicochemical properties of catalysts were characterized by BET, XRD, SEM, H-2-TPR, XPS and NH3-TPD. The characterization results showed that when La was loaded, the catalyst Ni/HZSM-5&La obtained a stronger medium-strong acidity. The electronic transfer of the elemental nickel was promoted. After HDO, the catalyst Ni/HZSM-5&La exhibited the highest HDO rate and BTX selectivity, reaching 97.79% and 34.25%, respectively. The real bio-oil HDO under a hydrogen donor were also analyzed. The results showed the content of the hydrocarbon compound were over 95%. The reaction mechanism was discussed through the distribution of liquid product species. Direct demethoxylation pathway (DMO) and methylation pathway (ME) were considered as the main pathways. (c) 2020 Elsevier Ltd. All rights reserved.
机译:氢供体由于其低的储存和运输成本而被用来代替纯氢作为原位气相HDO的氢源。通过用多金属和多载体改性沸石HZSM-5,已经制备了一系列催化剂。在2 MPa的压力和350℃的温度下对愈创木酚进行气相加氢脱氧(HDO)。研究了多金属和多载体改性对HDO活性的影响。通过BET,XRD,SEM,H-2-TPR,XPS和NH3-TPD对催化剂的理化性质进行了表征。表征结果表明,负载La时,Ni / HZSM-5&La催化剂具有较强的中强酸性。促进了镍元素的电子转移。 HDO后,Ni / HZSM-5&La催化剂表现出最高的HDO速率和BTX选择性,分别达到97.79%和34.25%。还分析了氢供体下的实际生物油HDO。结果表明,该烃类化合物含量在95%以上。通过液体产物种类的分布讨论了反应机理。直接脱甲氧基化途径(DMO)和甲基化途径(ME)被认为是主要途径。 (c)2020 Elsevier Ltd.保留所有权利。

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