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Ni,Co/SiO2 and Ni/SiO2,Co bimetallic microsphere catalysts indicating high activity and stability in the dry reforming of methane

机译:Ni,Co / SiO2和Ni / SiO2,Co双金属微球催化剂,表明甲烷干燥重整的高活性和稳定性

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Two separate synthesis procedures were applied to alter the location of Cobalt (Co) in bimetallic silica (SiO2) microsphere catalyst with Nickel (Ni) as the second active metal. Co was either encapsulated with simultaneous Ni addition inside core structure (Ni,Co/SiO2) or impregnated on the shell following initial encapsulation of Ni inside the microsphere (Ni/SiO2&Co). Catalysts were tested in dry reforming of methane (DRM) reaction at 750 degrees C with a feed mixture of CH4:CO2:N-2 = 1:1:1. Reactions were performed in a stainless steel temperature-controlled tube reactor. Results indicated the highest activity values with 4Ni-1Co ratio in catalyst structure and Co impregnated on catalyst structure revealed higher activity for all loadings compared to Ni,Co/SiO2 catalysts. CH4 and CO2 conversions for 3 h of reaction were obtained as 87 and 94%, and H-2/CO ratio was determined as 0.84 in the presence of Ni/SiO2&Co catalyst with 4Ni-1Co loading. Coke formation was not detected for the catalyst with 4Ni-1Co loading and the highest coke amount was 2% among all catalysts. Time on stream test in the presence of Ni/SiO2&Co catalyst with 4Ni-1Co loading was conducted for 12 h in identical conditions, and results revealed a stable activity with conversions equal to 3 h of reaction. Coke suppression during DRM reaction was attributed to microsphere structure, Co presence and SiC formation. SiC formation was introduced as a unique situation emanated as a result of the reaction between SiO2 and C.
机译:施加两个单独的合成程序以改变二氧化硅(SiO 2)微球催化剂中钴(CO)与镍(Ni)作为第二活性金属的位置。在微球内Ni的初始封装后,CO封装在核心结构(Ni,Co / SiO 2)内或浸渍在壳体上浸渍在壳体上(Ni / SiO 2&Co)。在750℃下在甲烷(DRM)反应的干燥重整中测试催化剂,用CH 4:CO 2:N-2 = 1:1:1的进料混合物。在不锈钢温度控制的管反应器中进行反应。结果表明,与Ni,Co / SiO 2催化剂相比,催化剂结构中的4Ni-1CO比和浸渍催化剂结构的CO浸渍的最高活性值显示出较高的所有载荷的活性。在Ni / SiO 2和Co催化剂存在下,得到3小时的CH 4和CO 2转化为87和94%,在Ni / SiO 2和Co催化剂存在下为0.84。未检测到催化剂的焦炭形成,其中4Ni-1CO负载,最高的焦炭量在所有催化剂中为2%。在Ni / SiO 2和Co催化剂存在下,在相同的条件下对Ni / SiO 2和Co催化剂的存在的时间在相同的条件下进行12小时,结果显示了等于反应3小时的转化率的稳定活性。 DRM反应期间的焦炭抑制归因于微球结构,CO存在和SiC形成。由于SiO2和C之间的反应而引入了SiC形成作为独特的情况。

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