高效Pd-Cu /TiO2双金属催化剂上BPZ高选择性裂解脱氢制备对苯基苯酚

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-08-13 DOI:10.1021/acsomega.5c05031
Chaofan Deng,  and , Chun Cai*, 
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引用次数: 0

摘要

采用浸渍还原法制备了用于双酚Z脱氢的钯铜双金属催化剂。采用XRD、HRTEM、XPS、BET和NH3-TPD等技术对所制得的催化剂进行了研究,并将其有效地应用于BPZ的高选择性裂解脱氢反应中,在270℃、常压、无溶剂条件下获得了99%的产率。结果表明,双金属催化剂的“协同效应”能有效促进裂解脱氢反应。Pd是H*吸附解离和C-H键活化的主要活性位点,而Cu则加速了C-H键的断裂过程。该催化剂稳定性好,可重复使用10次以上,收率和选择性均无明显下降。根据实验结果,提出了可能的反应途径,阐明了解理脱氢机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly Selective Cleavage Dehydrogenation of BPZ for Preparation of p-Phenylphenol over Efficient Pd–Cu/TiO2 Bimetallic Catalysts

Pd–Cu bimetallic catalysts were successfully synthesized for the dehydrogenation of Bisphenol Z (BPZ) by an impregnation-reduction method. The obtained catalyst was studied by XRD, HRTEM, XPS, BET, and NH3-TPD techniques and effectively applied in the highly selective cleavage dehydrogenation of BPZ to give PPP > 99% yield at 270 °C and atmospheric pressure in the solvent-free condition. It was demonstrated that the “synergistic effect” of the bimetallic catalysts could effectively promote the cleavage dehydrogenation reaction. Pd species served as the primary active sites for the adsorption and dissociation of H* and the activation of C–H bonds, while the introduced Cu species accelerated the breaking process of the C–H bond. This catalyst demonstrated remarkable stability and could be reused over ten cycles without obvious decrease both in yield and selectivity. The likely reaction pathway was outlined to elucidate the cleavage dehydrogenation mechanism according to experimental results.

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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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