NiMoAl catalysts derived from heptamolybdate-intercalated layered double hydroxides for hydrodeoxygenation of anisole

Chuang Li, Xingzhao Zhang, Xiao Chen, Zhijian Peng, Chi-Wing Tsang, Changhai Liang
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引用次数: 4

Abstract

The catalytic performance of NiMoAl catalysts derived from layered double hydroxide (LDH) precursors with molybdenum species incorporated into the interlayers was investigated for the hydrodeoxygenation (HDO) of anisole as a model compound of the lignin. The results showed that high dispersion of small Ni nanoparticles with 2–5?nm due to the pinning effect of Mo from Mo7O246? intercalated the LDHs. Due to presence of the oxygen vacancy sites on the molybdenum oxide, the NiMoAl catalysts exhibit higher conversion of anisole than the corresponding NiAl catalyst. The activity for hydrodeoxygenation was enhanced with the increased content of molybdenum species, which can be attributed to the larger amount of acid sites-promoted removal of oxygen from anisole. In addition, the NiMoAl catalysts show higher resistance to deactivation than the NiAl catalyst, and can be broadly applied to other hydrodeoxygenation reactions.

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由七钼酸盐插层双氢氧化物制备的苯甲醚加氢脱氧镍铝催化剂
以层状双氢氧化物(LDH)为前驱体,在层间掺入钼,研究了NiMoAl催化剂对木质素模型化合物苯甲醚的加氢脱氧(HDO)催化性能。结果表明,2-5 ?由于Mo7O246中Mo的钉住作用,插入LDHs。由于氧化钼上存在氧空位,NiMoAl催化剂的苯甲醚转化率高于相应的NiAl催化剂。随着钼含量的增加,氢脱氧活性增强,这可能是由于酸位促进了苯甲醚中氧的脱除。此外,NiMoAl催化剂比NiAl催化剂具有更高的抗失活能力,可广泛应用于其他加氢脱氧反应。
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