Hydrophobic Polyhedral Oligomeric Silsesquioxane Support Enhanced Methanol Production from CO2 Hydrogenation

倍半硅氧烷 材料科学 甲醇 催化作用 硅氧烷 煅烧 化学工程 选择性 合成气 纳米颗粒 有机化学 纳米技术 聚合物 复合材料 化学 工程类
作者
Yanet Rodríguez Herrero,Aman Ullah
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
被引量:7
标识
DOI:10.1021/acsami.3c00183
摘要

The abundance of CO2 from the cement industry, power generation, petroleum production, and combustion of biomass makes it a readily available feedstock to produce chemicals and materials, although it has yet to achieve optimal development. Even though syngas (CO + H2) hydrogenation to methanol is an established industrial process, when the same catalytic system based on Cu/ZnO/Al2O3 is employed with CO2, the water formed as a byproduct reduces the activity, stability, and selectivity of the process. Here, we explored the potential of phenyl polyhedral oligomeric silsesquioxane (POSS) as a hydrophobic support of Cu/ZnO for direct CO2 hydrogenation to methanol. Mild calcination of the copper–zinc-impregnated POSS material affords the formation of CuZn-POSS nanoparticles with Cu and ZnO homogeneously dispersed with an average particle size of 7 and 15 nm supported on O-POSS and D-POSS, respectively. The composite supported on D-POSS was able to reach a 3.8% yield of methanol with a 4.4% of CO2 conversion and with selectivity as high as 87.5% within 18 h. The structural investigation of the catalytic system reveals that CuO/ZnO are electron withdrawers in the presence of the siloxane cage of POSS. The catalytic system metal-POSS is stable and recyclable under H2 reduction and CO2/H2 conditions. We tested the use of microbatch reactors in heterogeneous reactions as a rapid and effective tool for catalyst screening. The increased number of phenyls in the structure of POSS results in an increased hydrophobic character that plays a decisive role in the methanol formation after comparison with CuO/ZnO supported on reduced graphene oxide with 0% selectivity to methanol under the study conditions. The materials were characterized using scanning electron microscopy, transmission electron microscopy, attenuated total reflection Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, powder X-ray diffraction, Fourier transform infrared analysis, Brunauer–Emmett–Teller specific surface area analysis, contact angle, and thermogravimetry. The gaseous products were characterized by gas chromatography coupled with thermal conductivity detectors and flame ionization detectors.
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