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首页> 外文期刊>ACS Omega >Hierarchically Structured Porous Spinels via an Epoxide-Mediated Sol–Gel Process Accompanied by Polymerization-Induced Phase Separation
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Hierarchically Structured Porous Spinels via an Epoxide-Mediated Sol–Gel Process Accompanied by Polymerization-Induced Phase Separation

机译:分层结构的多孔尖晶石,通过环氧介导的溶胶-凝胶过程,伴随聚合诱导相分离

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Enhancing the activity and stability of catalysts is a major challenge in scientific research nowadays. Previous studies showed that the generation of an additional pore system can influence the catalytic performance of porous catalysts regarding activity, selectivity, and stability. This study focuses on the epoxide-mediated sol–gel synthesis of mixed metal oxides, NiAl_(2)O_(4) and CoAl_(2)O_(4), with a spinel phase structure, a hierarchical pore structure, and Ni and Co contents of 3 to 33 mol % with respect to the total metal content. The sol–gel process is accompanied by a polymerization-induced phase separation to introduce an additional pore system. The obtained mixed metal oxides were characterized with regard to pore morphology, surface area, and formation of the spinel phase. The Brunauer–Emmett–Teller surface area ranges from 74 to 138 m~(2)·g~(–1) and 25 to 94 m~(2)·g~(–1) for Ni and Co, respectively. Diameters of the phase separation-based macropores were between 500 and 2000 nm, and the mesopore diameters were 10 nm for the Ni-based system and between 20 and 25 nm for the cobalt spinels. Furthermore, Ni–Al spinels with 4, 5, and 6 mol % Ni were investigated in the dry reforming of CH_(4) (DRM) with CO_(2) to produce H_(2) and CO. CH_(4) conversions near the thermodynamic equilibrium were observed depending on the Ni content and reaction temperature. The Ni catalysts were further compared to a noble metal-containing catalyst based on a spinel system showing comparable CH_(4) conversion and carbon selectivity in the DRM.
机译:如今,提高催化剂的活性和稳定性是科学研究的主要挑战。先前的研究表明,在活性,选择性和稳定性方面,附加孔隙系统的产生会影响多孔催化剂的催化性能。这项研究的重点是具有尖晶石相结构,分层孔结构以及Ni和Co的混合金属氧化物NiAl_(2)O_(4)和CoAl_(2)O_(4)的环氧化物介导的溶胶-凝胶合成。相对于总金属含量,其含量为3至33mol%。溶胶-凝胶过程伴随着聚合反应引起的相分离,从而引入了额外的孔隙系统。关于孔的形态,表面积和尖晶石相的形成,对获得的混合金属氧化物进行了表征。 Ni和Co的Brunauer-Emmett-Teller表面积分别为74至138 m〜(2)·g〜(-1)和25至94 m〜(2)·g〜(-1)。基于相分离的大孔的直径在500至2000 nm之间,对于基于镍的系统,中孔直径为10 nm,对于钴尖晶石,中孔直径为20至25 nm。此外,在将CH_(4)(DRM)与CO_(2)进行干重整以产生H_(2)和CO的过程中,研究了具有4、5和6 mol%Ni的Ni–Al尖晶石。根据Ni含量和反应温度观察到热力学平衡。进一步将Ni催化剂与基于尖晶石系统的含贵金属催化剂进行了比较,显示出可比的CH_(4)转化率和DRM中的碳选择性。

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