Polyethylene glycol promoted Cs/Zr-SiO2 bifunctional catalyst for aldol condensation of methyl propionate and formaldehyde to methyl methacrylate

被引:0
|
作者
Liu, Junyang [1 ,2 ,3 ]
Deng, Senlin [2 ]
Zhang, Guoliang [2 ,4 ]
Li, Jie [2 ]
Wang, Gang [2 ]
Li, Chunshan [1 ,2 ]
Li, Zengxi [1 ,3 ]
机构
[1] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[2] Chinese Acad Sci, Inst Proc Engn, State Key Lab Mesosci & Engn, CAS Key Lab Green Proc & Engn,Beijing Key Lab Ion, Beijing 100190, Peoples R China
[3] Binzhou Inst Technol, Weiqiao UCAS Sci & Technol Pk, Binzhou 256606, Peoples R China
[4] Xinjiang Zhongyou Puhui Technol Co Ltd, Hami 839304, Xinjiang, Peoples R China
基金
北京市自然科学基金;
关键词
Methyl methacrylate; Aldol condensation; Polyethylene glycol; Acid-base balance; Kinetics; Deactivation; CO METHANATION; NANOPARTICLES; SILICA; ACIDS;
D O I
10.1016/j.cej.2024.156417
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The production of methyl methacrylate (MMA) via one-step gaseous aldol condensation of methyl propionate (MP) and formaldehyde (FA) has received wide attention. Herein, series of polyethylene glycol (PEG) promoted Cs-Zr/SiO2 catalysts were developed and characterized by XRD, FT-IR, HR-TEM, BET, NH3-/CO2-TPD and Py-IR etc. The dispersion of active acid and base sites and their balance in catalyst could be significantly improved with the addition of PEG, which facilitated the activation of reactants and conversion towards product MMA. Furthermore, the relationship between the acid-base properties and catalytic performance was revealed, the acid and base sites were responsible for the decomposition of trioxane, which was used as the source of FA, and transformation of MP, respectively. The in-situ DRIFTS experiments unraveled two catalytic pathways through the synergistic effects between the acid and base sites during the aldol condensation of MP with FA to MMA. Kinetic studies revealed that the activation energy of this aldol condensation on the optimal catalyst is 97.9 kJ/ mol, with the reaction order of 0.98 and 1.18 corresponding to MP and FA. Deactivation behavior studies demonstrated that the decrease of catalytic activity as a function of time-on-stream was resulting from the deposition of predominant amorphous carbon instead of the loss of active components.
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页数:13
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