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首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >Mesostructured CMK-3 carbon supported Ni-ZrO2 as catalysts for the hydrodeoxygenation of guaiacol
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Mesostructured CMK-3 carbon supported Ni-ZrO2 as catalysts for the hydrodeoxygenation of guaiacol

机译:西部结构化的CMK-3碳负载Ni-ZrO2作为Guaiacol的加氢脱氧的催化剂

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摘要

In this work, mesoporous carbon materials were obtained by using the nanocasting method starting from ordered mesoporous SBA-15 and commercial nonporous Cab-O-sil (R) M - 5 silica hard templates; materials were named CMK-3 and C-Cab, respectively. These carbon materials, displaying different porous structures (mesopore diameter, specific surface area and pore volume) were used to stabilize Ni and ZrO2 particles using different deposition methods for the nickel and zirconium phases. The catalysts were tested in the hydrodeoxygenation of guaiacol. The conversion varied from 40 to 100% depending on the textural properties of the carbon support and reaction time at 300 degrees C and under 50 bar of hydrogen pressure. The catalysts were selective toward the formation of the hydrogenation product (methoxycyclohexanol) and hydrogenated - partially deoxygenated product (cyclohexanol). The deposition of the Ni and ZrO2 precursors in mesoporous CMK-3 carbon replicas with a unimodal mesopore diameter, with respect to the use of non-ordered carbons, allows to obtain improved selectivity toward cyclohexanol and, more importantly, toward cyclohexane. Preparation using incipient-wetness impregnation favoured the formation of both monoclinic and tetragonal phases, while the deposition-precipitation method led to the formation of ZrO2 with a unique tetragonal structure. The presence of both monoclinic and tetragonal phases modified the density of catalyst acid sites, which allow to improve the selectivity toward cyclohexane and cyclohexanol while decreasing the selectivity toward the undesired methoxycyclohexanol and other oxygenated compounds.
机译:在这项工作中,通过使用从有序的介孔SBA-15和商业无孔驾驶室-O-SIL(R)M-5二氧化硅硬模板开始的纳米占用方法获得了介孔的碳材料;材料分别命名为CMK-3和C-CAB。这些碳材料,显示不同的多孔结构(中孔直径,比表面积和孔体积)来使用不同的沉积方法稳定Ni和ZrO 2颗粒,用于镍和锆相。在Guaiacol的加氢脱氧中测试催化剂。转化率根据碳载体的纹理性质和300摄氏度下的反应时间和50巴的氢气压力而变化。催化剂朝向形成氢化产物(甲氧基环己醇)和氢化 - 部分脱氧产物(环己醇)的形成。关于使用非订购的碳的介孔CMK-3碳复制品中的Ni和ZrO2前体的沉积,允许从无定碳碳的渗透率直径允许改善对环己醇的改善的选择性,更重要的是朝向环己烷。使用初期湿度浸渍的制备有利于形成单斜晶和四方相的形成,而沉积沉淀方法导致ZrO2的形成具有独特的四方结构。单斜晶和四边形相的存在改性了催化剂酸的密度,其允许改善环己烷和环己醇的选择性,同时降低对不需要的甲氧基环己醇和其它含氧化合物的选择性。

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