苯乙炔
催化作用
选择性
钯
X射线光电子能谱
吸附
扫描电子显微镜
聚合物
化学
苯乙烯
纳米颗粒
核化学
材料科学
无机化学
化学工程
有机化学
共聚物
纳米技术
复合材料
工程类
作者
Assemgul S. Auyezkhanova,Eldar T. Talgatov,Sandugash N. Akhmetova,Aigul I. Jumekeyeva,Akzhol A. Naizabayev,Aigul T. Zamanbekova,Makpal K. Malgazhdarova
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2025-09-19
卷期号:30 (18): 3820-3820
标识
DOI:10.3390/molecules30183820
摘要
In this study, we investigated the influence of polymer nature and support characteristics on the performance of Pd-based heterogeneous catalysts. Catalysts were prepared via sequential adsorption of poly(4-vinylpyridine) (P4VP) or chitosan (CS) and palladium ions onto MgO and SBA-15 supports under ambient conditions. The resulting hybrid materials were characterized by IR spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectra (XPS). TEM analysis revealed that Pd nanoparticles with an average size of 2–3 nm were well-dispersed on P4VP/MgO, while larger and less uniformly distributed particles (8–10 nm) were observed on SBA-15-based systems. Catalytic tests in the hydrogenation of 2-propen-1-ol, phenylacetylene, and 2-hexyn-1-ol under mild conditions (40 °C, 1 atm H2, ethanol) demonstrated that both the support and polymer type significantly influence activity and selectivity. P4VP-modified catalysts outperformed CS-containing analogs in all reactions. MgO-based systems showed higher activity and selectivity in 2-propen-1-ol hydrogenation compared to SBA-15-based catalysts. The 1%Pd–P4VP/MgO catalyst exhibited the best performance, with a reaction rate of 5.2 × 10−6 mol/s, 83.4% selectivity to propanol, and stable activity over 30 consecutive runs. In phenylacetylene and 2-hexyn-1-ol hydrogenation, all catalysts showed high selectivity to styrene (93–95%) and cis-2-hexen-1-ol (96–97%), respectively. The incorporation of P4VP polymer into the Pd/MgO catalyst leads to smaller and better-distributed palladium particles, resulting in enhanced catalytic activity and stability during hydrogenation reactions. These results confirm that the choice of polymer modifier and inorganic support must be tailored to the specific reaction, enabling the design of highly active and selective polymer-modified Pd catalysts for selective hydrogenation processes under mild conditions.
科研通智能强力驱动
Strongly Powered by AbleSci AI