Chunxiang Li
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Chunxiang Li has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
Jianming Pan
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, P. R. China
1 shared publicationLongcheng Xu
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, P. R. China
1 shared publicationWei Guan
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, PR China
1 shared publicationWei Hu
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, P. R. China
1 shared publicationXiaohua Zou
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, P. R. China
1 shared publicationXue Wang
College of Chemistry and Chemical Engineering, Jiangsu University, Zhenjiang, P. R. China
1 shared publication
Latest Publications
- 15 April 2011
- Published by Wiley in Journal of Separation Science
- Vol. 34 (11) , 1244-1252
Selective recognition of 4‐nitrophenol from aqueous solution by molecularly imprinted polymers with functionalized tetratitanate whisker composites as support
Three kinds of molecularly imprinted polymers (MIPs) were obtained with surface molecular imprinting technique on functionalized potassium tetratitanate whisker (F‐PTW). The results of adsorption experiments indicated that MIP prepared using PTW modified with N‐(2‐aminoethyl)‐3‐(trimethoxysilyl)propylamine (AAPTS) (F‐PTW A) as support [MIP(1)] was superior to the other two polymers, then MIP(1) was selected to analyze the 4‐nitrophenol (4‐NP) adsorption process from aqueous solution in this study. AAPTS offered hydrophilic exterior that allowed to self‐assemble with the template 4‐NP through intermolecular interaction rather than based on the interactions between the functional monomers and template. Equilibrium adsorption data were analyzed by the Langmuir and Freundlich isotherm models at various temperatures. Kinetic properties were successfully investigated by pseudo‐first‐order model, pseudo‐second‐order model, intraparticle diffusion equation, initial adsorption rate, half‐adsorption time. A diffusion‐controlled process as the essential adsorption rate‐controlling step was also proposed. The performance of such imprinted polymer was further demonstrated by high‐performance liquid chromatography, and the results showed that the selectivity of MIP(1) exhibited higher affinity for template 4‐NP over competitive phenolic compounds than that of non‐imprinted polymer NIP(1). MIP(1) could be reused four times without significant loss in the adsorption capacity.
- 15 April 2011
- Published by Wiley in Journal of Separation Science
- Vol. 34 (11) , 1244-1252
Selective recognition of 4‐nitrophenol from aqueous solution by molecularly imprinted polymers with functionalized tetratitanate whisker composites as support
Three kinds of molecularly imprinted polymers (MIPs) were obtained with surface molecular imprinting technique on functionalized potassium tetratitanate whisker (F‐PTW). The results of adsorption experiments indicated that MIP prepared using PTW modified with N‐(2‐aminoethyl)‐3‐(trimethoxysilyl)propylamine (AAPTS) (F‐PTW A) as support [MIP(1)] was superior to the other two polymers, then MIP(1) was selected to analyze the 4‐nitrophenol (4‐NP) adsorption process from aqueous solution in this study. AAPTS offered hydrophilic exterior that allowed to self‐assemble with the template 4‐NP through intermolecular interaction rather than based on the interactions between the functional monomers and template. Equilibrium adsorption data were analyzed by the Langmuir and Freundlich isotherm models at various temperatures. Kinetic properties were successfully investigated by pseudo‐first‐order model, pseudo‐second‐order model, intraparticle diffusion equation, initial adsorption rate, half‐adsorption time. A diffusion‐controlled process as the essential adsorption rate‐controlling step was also proposed. The performance of such imprinted polymer was further demonstrated by high‐performance liquid chromatography, and the results showed that the selectivity of MIP(1) exhibited higher affinity for template 4‐NP over competitive phenolic compounds than that of non‐imprinted polymer NIP(1). MIP(1) could be reused four times without significant loss in the adsorption capacity.