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Merrifield树脂
Atmospheric Pollution Research · 2018 · IF 2.152

Investigation of low concentration SO2 adsorption performance on different amine-modified Merrifield resins

Xiao Yu,Jinliang Hao,Zhicheng Xi,Taiyang Liu,Ying Lin,Bin Xu

Three amine-modified Merrifield resins (AMMRs) were synthesized with ethane diamine, methylamine and dimethylamine to assess the impact of amine group on SO 2 adsorption under low SO 2 concentration. The dimethylamine-modified Merrifield resin (DMAMR) grafting with tertiary amine groups showed the greatest SO 2 adsorption compared with ethane diamine-modified Merrifield resin (EDAMR) and methylamine-modified Merrifield resin (MAMR). Different amine groups had different reaction mechanisms with SO 2 . It was much easier for SO 2 to form noncovalent charge transfer complex with tertiary amine group than the zwitterion and ion/counterion products with primary and secondary amine groups under dry condition. The noncovalent charge transfer complex had a relatively weaker thermostability than the zwitterion and ion/counterion products. As the temperature increased from 25 °C to 75 °C, the SO 2 adsorption capacity on DMAMR decreased by 78.92%, which was much higher than that of EDAMR and MAMR (63.77% and 63.41% respectively). As SO 2 concentration increased from 40 ppm to 100 ppm, significant increase (∼100%) in SO 2 adsorption capacity was observed. Lower SO 2 flow rate led to a more sufficient reaction between SO 2 and amine groups, resulting the increase in SO 2 adsorption capacities. Water vapor enhanced the SO 2 adsorption performance of AMMRs significantly due to the formation of salt. However, it was more difficult for tertiary amine group to react with SO 2 in the presence of water due to its relatively weaker basicity . DMAMR showed a greater regeneration performance than EDAMR and MAMR under dry and humid condition.

研究领域: 环境科学 · 化学工程
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CHEMICAL ENGINEERING JOURNAL · 2015 · IF 4.321

Efficient oxidation of biomass derived 5-hydroxymethylfurfural into 2,5-furandicarboxylic acid catalyzed by Merrifield resin supported cobalt porphyrin

Langchang Gao,Kejian Deng,Judun Zheng,Bing Liu,Zehui Zhang

In this study, a new method was developed for the oxidation of 5-hydroxymethylfurfural (HMF) into 2,5-furandicarboxylic acid (FDCA) over Merrifield resin supported Co(II)–meso-tetra(4-pyridyl)-porphyrin (abbreviated as Merrifield resin-Co-Py). Diffuse reflectance spectra showed that Co(II)–meso-tetra(4-pyridyl)-porphyrin was successfully bonded on the Merrifield resin. The Merrifield resin-Co-Py catalyst was used for the oxidation of HMF into FDCA, and several parameters were studied. Tert-butyl hydroperoxide was the best oxidant among other common oxidants. The reaction solvent greatly affected both HMF conversion and product selectivity. High HMF conversion of 95.6% and FDCA yield of 90.4% were obtained at 100   °C after 24   h. Time course of HMF conversion over Merrifield resin-Co-Py showed that 2,5-diformylfuran was the intermediate for the conversion of HMF into FDCA. The catalyst could be reused without the significant loss of its catalytic activity.

研究领域: 化学工程 · 生物质转化 · 催化化学
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