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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >In-situ hydrodeoxygenation of a mixture of oxygenated compounds with hydrogen donor over ZrNi/Ir-ZSM-5+Pd/C
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In-situ hydrodeoxygenation of a mixture of oxygenated compounds with hydrogen donor over ZrNi/Ir-ZSM-5+Pd/C

机译:用ZrNI / IR-ZSM-5 + PD / C的含氧化合物的含氧化合物混合物的原位加氢脱氧

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In-situ hydrodeoxygenation of a mixture of oxygenated compounds from bio-oil with hydrogen donor over supported multi-metal catalysts was investigated. As most previous in-situ hydrodeoxygenation reports focused on phenols, guaiacol, furfural, and acetic acid, this paper extends the scope to a mixture of oxygenated compounds of not only phenols, guaiacol, furfural and acetic acid, but also of lesser reported hydroxyl -propanone, cyclopentanone aiming at obtaining more liquid fuels. The method of incipient wetness impregnation was used to load the three metals (Zr, Ni, Ir) and Pd on the support of ZSM-5 and C, respectively. The conversion of acetic acid, hydroxyl -propanone, cyclopentanone, guaiacol, furfural, and phenol reached 99.7%, 99.3%, 100%, 100%, 100%, and 100%, respectively, including the total deoxygenation ratio of 99.6%, the liquid yield (96.5%), and the hydrocarbon yield (86.7%), under the suitable conditions. The sulfur content, the octane number, and the H/C ratio of bio-oil through in-situ hydrodeoxygenation have been improved, and reached 0, 89 and 1.9, respectively. We also speculated reaction pathways of different oxides according to the product distribution over ZrNi/Ir-ZSM-5 and Pd/C. (C) 2018 Elsevier B.V. All rights reserved.
机译:研究了与氢供体在负载的多金属催化剂上的生物油混合物的原位加氢脱氧。作为大多数以前的原位加氢脱氧报告集中于酚,胍,糠醛和乙酸,本文将范围延伸到不仅酚,胍,糠醛和乙酸的含氧化合物的混合物,还将较小的羟基 - 丙酮,环戊酮旨在获得更多液体燃料。初期湿润浸渍的方法用于将三种金属(Zr,Ni,IR)和Pd加载到ZSM-5和C的载体上。乙酸,羟丙酮,环戊酮,胍,糠醛和苯酚的转化率分别达到99.7%,99.3%,100%,100%,100%和100%,包括总脱氧比为99.6%,在合适的条件下,液体产率(96.5%)和烃产率(86.7%)。通过原位加氢脱氧的生物油的硫含量,辛烷值和H / C比分别得到改善,分别达到0,89和1.9。我们还根据ZrNI / IR-ZSM-5和Pd / C的产物分布推测不同氧化物的反应途径。 (c)2018年elestvier b.v.保留所有权利。

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