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Pd/H-MOR
CHEMICAL ENGINEERING JOURNAL · 2026 · IF 12.5

Hydrogenation of CO2 to formate/formic acid over Pd/H-MOR

Faisal Irshad,Dan Zhang,Hamzah A.S.M. Yaseen,Xianming Zhu,Muhammad Chawla,Shengping Wang,Yongli Shen,Xinbin Ma

Pd/H-MOR exhibits superior catalytic activity and stability for CO 2 hydrogenation to formateover other Pd/Zeolites and M/H-MOR. • Brønsted acid sites at Pd-H-MOR interface polarize CO 2 , while highly dispersed Pd nanoparticles dissociate H 2 barrierlessly. • Low Si/Al ratio optimizes metal-support synergy and reducing apparent activation energy to HCOOH. • Bicarbonate identified as the key reaction intermediates by in-situ DRIFTS and DFT study. Catalytic hydrogenation is a promising route for CO 2 conversion, yet the highly efficient formation of formic acid remains challenging. Herein, Pd nanoparticles dispersed on mordenite (Pd/H-MOR) are reported as an efficient and stable catalyst for CO 2 hydrogenation to produce formates. Under optimized conditions, Pd/H-MOR achieved an intrinsic turnover number of 1828 and a turnover frequency of 914 h −1 at 120 °C, surpassing all the other prepared catalysts with different metal active sites and zeolite supports. The high activity arises from the co-effect of Pd and the H-MOR support: Pd sites dissociate H 2 into active hydrogen, while Brønsted acid sites enhance CO 2 adsorption via polarization and stabilize bicarbonate intermediates, which subsequently convert to formates. Density functional theory (DFT) results revealed that Pd/H-MOR lowers the activation barriers for both H 2 dissociation and CO 2 activation at the Pd-MOR interface and combined with in-situ DRIFTS, identifying surface bicarbonates as the key reactive intermediates en-route to formate formation. Comparatively, kinetic studies of Pd/H-MOR revealed a reduced apparent activation energy of 15.81 ± 0.79 kJmol −1 , reflecting strong metal-support interactions, while the observed R = k ∙ P CO 2 0.56 ∙ P H 2 0.62 R=k∙PCO20.56∙PH20.62 reaction orders indicate that the reaction rate is weakly dependent of H 2 and CO 2 pressures but strongly dependent on the nature of the metal and the zeolite support. This work highlights metal dispersion and support acidity as key factors for CO 2 hydrogenation. Download: Download high-res image (224KB) Download: Download full-size image

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Journal of Environmental Sciences · 2023 · IF 6.9

Lean methane combustion over zeolite-supported Pd catalysts: Structure-performance relationship and deactivation mechanism

Xingyu Liu,Jingkun Chen,Bowen Han,Renna Li,Le Shi,Zhongbiao Wu,Xiaole Weng

Zeolites are a promising support for Pd catalysts in lean methane (CH 4 ) combustion. Herein, three types of zeolites (H-MOR, H-ZSM-5 and H-Y) were selected to estimate their structural effects and deactivation mechanisms in CH 4 combustion. We show that variations in zeolite structure and surface acidity led to distinct changes in Pd states. Pd/H-MOR with external high-dispersing Pd nanoparticles exhibited the best apparent activity, with activation energy ( E a ) at 73 kJ/mol, while Pd/H-ZSM-5 displayed the highest turnover frequency (TOF) at 19.6 × 10 −3  s −1 , presumably owing to its large particles with more step sites providing active sites in one particle for CH 4 activation. Pd/H-Y with dispersed PdO within pore channels and/or Pd 2+ ions on ion-exchange sites yielded the lowest apparent activity and TOF. Furthermore, Pd/H-MOR and Pd/H-ZSM-5 were both stable under a dry condition, but introducing 3 vol.% H 2 O caused the CH 4 conversion rate on Pd/H-MOR drop from 100% to 63% and that on Pd/H-ZSM-5 decreased remarkably from 82% to 36%. The former was shown to originate from zeolite structural dealumination, and the latter principally owed to Pd aggregation and the loss of active PdO.

CAS / MDL: 313222-87-6
研究领域: 催化 · 化学工程 · 环境科学
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