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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 · IF 7.139

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

Hui Wang,Hao Zhu,Yuelan Zhang,Jianglong Pu

A 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 , H 2 -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 CeO 2 , 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 CO 2 /CO ratio in the products. Much more CO and CO 2 and less CH 4 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 .

研究领域: 化学工程 · 催化材料科学
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JOURNAL OF MATERIALS SCIENCE · 2018 ·Vol. 54 ·期 7 ·5359-5365 · IF 2.993

Surfactant-assisted synthesis of a novel macroporous tin organophosphonate with mesoporous walls

Guo Bing,Lin Xiuzhen

A novel hierarchically mesoporous–macroporous tin organophosphonate with intra-framework organic groups is successfully fabricated through a facile hydrothermal route with SnCl 4 ·5H 2 O as tin source and diethylene triamine pentakis(methylphosphonic acid) as organophosphorus source in the presence of cetyltrimethylammonium bromide (CTAB) as the templating agent. The as-prepared hybrid had macroporous structures with the pore size in the range of 0.6–2.1 μm and a specific surface area of 170 m 2 /g. Besides, the pore walls had particle-aggregated mesoporous substructures, consisting of amorphous tin organophosphonates, as characterized by SEM, TEM and N 2 adsorption analysis and wide- and low-angle X-ray diffraction. FT-IR and NMR results indicated the integrity of the organophosphonate groups into the hybrid solid. It was found that the surfactant CTAB played an important role in obtaining macropores, and a possible formation route was proposed.

研究领域: 材料科学 · 化学工程
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