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Highly active Ni/CeO2 for the steam reforming of acetic acid using CTAB as surfactant template

机译:以CTAB为表面活性剂模板的高活性Ni/CeO2用于醋酸的蒸汽重整

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? 2022 Hydrogen Energy Publications LLCA series of CTAB-templated Ni/Ce catalysts were synthesized by adding CTAB during the hydrothermal synthesis of ceria to improve the pore structure of catalysts. Their catalytic performance was evaluated in the steam reforming of acetic acid and the effects of CTAB concentration on the porous structures, reducibilities, morphology, and activity of catalysts were studied. The catalysts were characterized by BET, XRD, H2-TPR, XPS, HRTEM, in-situ DRIFTS, DTG, FTIR, and temperature-programmed reaction to elucidate the structure-activity relationship of the catalyst. The results showed that owing to the CTAB assistance, a high surface area of ceria could be achieved, which induced a better Ni dispersion with a smaller Ni size, strengthened the interaction between Ni and CeO2, and promoted the reducibility of Ni, obtaining higher activity and lower methane yield than Ni/Ce. Among these prepared samples, Ni/Ce–C6 showed the highest surface area and the best catalytic performance with a hydrogen yield of up to 82.5 even at a low temperature (550 °C). Owing to the stronger Ni-ceria interaction of Ni/Ce–C6, the lattice oxygen in ceria migrates easily to the Ni surface, interacts with the reaction intermediates, and thus improves the CO2/CO ratio in the products. Much more CO and CO2 and less CH4 were observed over Ni/Ce–C6 during the temperature-programmed reaction, indicating its high activity. In-situ DRFITS characterization demonstrated that the two types of catalysts had similar reaction intermediates but various adsorption and conversion abilities toward the acetic acid. More reaction intermediates were adsorbed at low temperatures and a higher conversion was obtained over Ni/Ce–C6 owing to its better Ni dispersion. The CTAB assistance inhibited the formation of amorphous carbon but facilitated the formation of graphitic carbon at ~637 °C which did not induce catalyst deactivation.
机译:?2022 Hydrogen Energy Publications LLCA系列CTAB模板化Ni/Ce催化剂是在水热合成铈过程中加入CTAB合成的,以改善催化剂的孔隙结构。评价了其在醋酸水蒸气重整中的催化性能,研究了CTAB浓度对催化剂多孔结构、还原性、形貌和活性的影响。通过BET、XRD、H2-TPR、XPS、HRTEM、原位漂移、DTG、FTIR和程序升温反应等手段对催化剂进行了表征,阐明了催化剂的构效关系。结果表明,在CTAB的辅助下,铈的表面积较高,Ni粒径更小,Ni分散性更好,Ni与CeO2相互作用增强,促进Ni的还原性,获得比Ni/Ce更高的活性和更低的甲烷产率。其中,Ni/Ce–C6的比表面积最大,催化性能最好,即使在低温(550 °C)下氢气收率也高达82.5%。由于Ni/Ce–C6的Ni-ceria相互作用较强,铈中的晶格氧容易迁移到Ni表面,与反应中间体相互作用,从而提高了产物中的CO2/CO比。在程序升温反应过程中,Ni/Ce–C6 的 CO 和 CO2 含量更高,CH4 更少,表明其活性很高。原位DRFITS表征表明,两种催化剂具有相似的反应中间体,但对乙酸的吸附和转化能力不同。在低温下吸附了更多的反应中间体,并且由于Ni/Ce-C6具有更好的Ni分散性,因此获得了更高的转化率。CTAB的辅助作用抑制了无定形碳的形成,但促进了~637 °C石墨碳的形成,这不会引起催化剂失活。

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