Guo Ying, Li Jinhong, Xu Qingxin, Song Zhimei, Wang Jinge, Han Mei, Chen Lidong, Han Na, Cheng Weiguo
Faculty of Chemistry and Chemical Engineering, Liaoning Normal University, 110629, Dalian, Liaoning, PR China.
Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices, Soochow University, 215123, Suzhou, PR China.
Chemistry. 2024 Apr 2;30(19):e202303739. doi: 10.1002/chem.202303739. Epub 2024 Feb 14.
To expand the market capacity of p-diethylbenzene (PDEB), core-shell zeolite (TS-1@MCM-48) is designed as a catalyst for PDEB oxidation. TS-1@MCM-48 catalyst is synthesized by in-situ crystallization method and characterized by X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), N adsorption-desorption, in-situ electron paramagnetic resonance (EPR) and Si nuclear magnetic resonance (Si MAS-NMR). Oxidation of PDEB by HO was investigated systematically in liquid phase. The conversion of PDEB over TS-1@MCM-48 was 28.1 % and the total selectivity was 72.6 %, where the selectivity of EAP (p-ethylacetophenone) and EPEA (4-ethyl-α-methylbenzyl alcohol) was 28.6 % and 44.0 %, respectively. Compared with TS-1 and MCM-48 zeolite, the conversion rate of reactants and the selectivity of products have been significantly improved. The catalytic performance of TS-1@MCM-48 is derived from its well-crystallized microporous core and mesoporous shell with regular channels, which make active sites of TS-1 zeolite in the catalyst be fully utilized and mass transfer resistance be largely reduced. Further through theoretical calculation, we propose that the oxidation of PDEB is the result of the combination and mutual transformation of free radical process and carbocation process. Core-shell structure ensures the conversion rate of raw materials and improves the selectivity of products.
为了扩大对二乙苯(PDEB)的市场容量,设计了核壳沸石(TS-1@MCM-48)作为PDEB氧化的催化剂。采用原位结晶法合成了TS-1@MCM-48催化剂,并通过X射线衍射(XRD)、透射电子显微镜(TEM)、扫描电子显微镜(SEM)、X射线光电子能谱(XPS)、N吸附-脱附、原位电子顺磁共振(EPR)和硅核磁共振(Si MAS-NMR)对其进行了表征。系统研究了HO在液相中对PDEB的氧化作用。TS-1@MCM-48上PDEB的转化率为28.1%,总选择性为72.6%,其中对乙基苯乙酮(EAP)和4-乙基-α-甲基苄醇(EPEA)的选择性分别为28.6%和44.0%。与TS-1和MCM-48沸石相比,反应物的转化率和产物的选择性都有显著提高。TS-1@MCM-48的催化性能源于其结晶良好的微孔核和具有规则孔道的介孔壳,这使得催化剂中TS-1沸石的活性位点得到充分利用,传质阻力大大降低。进一步通过理论计算,我们提出PDEB的氧化是自由基过程和碳正离子过程结合及相互转化的结果。核壳结构保证了原料的转化率,提高了产物的选择性。