生物油模型化合物愈创木酚在Ce-Fe/Al2O3催化剂上的原位脱氧性能研究

Meiling Yang , Yanming Chen , Yong Wang , Laishun Yang , Weiwei Cui , Yanhui Liu , Cuiping Wang , Qun Chen
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引用次数: 0

摘要

愈创木酚(GUA,一种模式生物油化合物)的低成本脱氧研究对生物油的改性具有重要意义。目前,用于GUA脱氧反应的常见硫化物催化剂会造成液体产物的污染,并且贵金属催化剂在经济上是不利的。本研究制备了四种不同Ce掺杂率的还原铁基氧化物,并探讨了它们对GUA在水/甲醇氢供体溶剂中原位脱氧性能的影响。基于产物的脱氧度、转化度和较高热值(HHV)的结果表明,在甲醇溶剂中Fe/Ce摩尔比为2:1的氧化物催化剂表现良好。在选择了优良的催化剂和较好的氢供体溶剂后,采用正交实验方法研究了影响GUA脱氧度的四个因素(反应温度、反应时间、GUA用量与甲醇用量的体积比、反应器底部与顶部催化剂用量的比例),以进一步探讨催化剂的性能。结果表明,反应温度和反应时间对GUA脱氧有很大影响。在最佳实验条件下,基于气相色谱-质谱的相对峰面积,GUA的脱氧度和转化度分别可达34.36%和92.56%,液体产物的HHV为32.27MJ/kg。尽管Fe/Ce催化剂主要促进脱甲氧基化、脱甲基化和甲基化,由于酚羟基和醚含量的降低,液体产物的稳定性和质量与GUA相比得到改善。X射线衍射和X射线荧光显示,还原催化剂在甲醇中的GUA原位脱氧反应过程中保持了稳定的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Investigation on in-situ deoxygenation performance of bio-oil model compound guaiacol over Ce-Fe/Al2O3 catalyst

Investigation on in-situ deoxygenation performance of bio-oil model compound guaiacol over Ce-Fe/Al2O3 catalyst

The investigation of the low-cost deoxygenation of guaiacol (GUA, a model bio-oil compound) is of importance for upgrading bio-oil. At present, common sulfide catalysts for GUA deoxygenation reactions cause contamination of the liquid product, and noble metal catalysts are economically disadvantageous. In this study, four reduced Fe-based oxides with different Ce doping ratios were prepared and their effects on the in-situ deoxygenation performance of GUA in aqueous/methanol hydrogen donor solvents were explored. The results based on the deoxygenation degree, conversion degree, and higher heating value (HHV) of the products showed that the oxide catalyst with a Fe/Ce molar ratio of 2:1 in the methanol solvent performed very well. After selecting an excellent catalyst and a better hydrogen donor solvent, four factors (reaction temperature, reaction time, volume ratio of GUA dosage and methanol dosage, and the ratio of catalyst dosage at the bottom of the reactor to that at the top) in the deoxygenation degree of GUA were investigated using an orthogonal experimental method to further explore the performance of the catalyst. The results showed that the reaction temperature and time greatly influenced GUA deoxygenation. Under optimal experimental conditions, the deoxygenation degree and conversion degree of GUA could reach 34.36% and 92.56%, respectively, based on the relative peak area of gas chromatography–mass spectrometry, and the HHV of the liquid product was 32.27 MJ/kg. Although Fe/Ce catalysts mainly promote demethoxylation, demethylation, and methylation, the stability and quality of the liquid products were improved compared with GUA owing to the reduction in phenolic hydroxyl and ether content. The reduced catalyst in the process of GUA in-situ deoxygenation reactions in methanol maintained a steady performance, as revealed by X-ray diffraction and X-ray fluorescence.

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