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镁铝水滑石/薄水铝石负载铂纳米粒子催化剂上甲醛的室温增强催化分解。

Enhanced room-temperature catalytic decomposition of formaldehyde on magnesium-aluminum hydrotalcite/boehmite supported platinum nanoparticles catalyst.

机构信息

Key Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of Education, Hubei Key Laboratory of Industrial Fume and Dust Pollution Control, Jianghan University, Wuhan 430056, PR China.

Key Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of Education, Hubei Key Laboratory of Industrial Fume and Dust Pollution Control, Jianghan University, Wuhan 430056, PR China.

出版信息

J Colloid Interface Sci. 2018 Aug 15;524:306-312. doi: 10.1016/j.jcis.2018.04.018. Epub 2018 Apr 5.

Abstract

Magnesium-aluminum hydrotalcite (Mg-Al HT)/boehmite (AlOOH) composite supported Pt catalysts were obtained via one-pot microemulsion synthesis of Mg-Al HT/AlOOH composite and NaBH-reduction of Pt precursor processes. The catalytic performances of the catalysts were evaluated for formaldehyde (HCHO) removal at room temperature. The performance tests showed that the catalyst obtained by immobilizing Pt nanoparticles (NPs) on Mg-Al HT/AlOOH support with Al/Mg molar ratio equivalent to 9:1 (Pt/AlMg) displayed a superior catalytic activity and stability for HCHO removal. In order to find out the causes of its higher activity, X-ray diffraction, transmission electron microscopy, N adsorption/desorption, X-ray photoelectron spectroscopy, temperature programmed desorption of CO and reduction of H were used to analyze the physicochemical properties of Pt/AlMg and Pt/AlOOH. The remarkable catalytic performance of Pt/AlMg is mainly attributed to the relatively larger amount of surface oxygen species, and more reactive oxygen species led by the interaction of Mg-Al HT and AlOOH/Pt, and relatively larger number of weak base sites caused by Mg-Al HT. The formate species are the main reaction intermediate over Pt/AlMg during HCHO oxidation at room temperature, which could be further oxidized into CO and HO in the presence of O. This study might shed some light on further improving the catalytic performance of the catalyst for indoor air purification at room temperature.

摘要

镁铝水滑石(Mg-Al HT)/薄水铝石(AlOOH)复合负载 Pt 催化剂通过 Mg-Al HT/AlOOH 复合的一锅微乳液合成和 Pt 前体的 NaBH 还原过程获得。在室温下,通过评价催化剂对甲醛(HCHO)去除的催化性能来测试其性能。性能测试表明,通过将 Pt 纳米颗粒(NPs)固定在 Al/Mg 摩尔比等于 9:1 的 Mg-Al HT/AlOOH 载体上(Pt/AlMg)的催化剂对 HCHO 的去除具有更高的催化活性和稳定性。为了找出其更高活性的原因,使用 X 射线衍射、透射电子显微镜、N2 吸附/脱附、X 射线光电子能谱、CO 程序升温脱附和 H2 还原来分析 Pt/AlMg 和 Pt/AlOOH 的物理化学性质。Pt/AlMg 的显著催化性能主要归因于表面氧物种的相对较大量,以及由 Mg-Al HT 和 AlOOH/Pt 的相互作用引起的更具反应性的氧物种,以及由 Mg-Al HT 引起的相对较大量的弱碱性位。在室温下 HCHO 氧化过程中,甲酸盐物种是 Pt/AlMg 上的主要反应中间体,在 O 的存在下,它可以进一步氧化成 CO 和 HO。本研究可能为进一步提高催化剂在室温下用于室内空气净化的催化性能提供一些启示。

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