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乙烯基功能化磁性分子印迹聚合物的制备和识别性能研究

Translated title of the contribution: Preparation and identification of vinyl functionalized magnetic molecularly imprinted polymers
  • Weiwei Huang
  • , Qianyu Zhao
  • , Xin Yang*
  • , Lei Yao
  • , Haitian Zhao
  • *Corresponding author for this work
  • School of Chemistry and Chemical Engineering, Harbin Institute of Technology
  • Northeast Agricultural University

Research output: Contribution to journalArticlepeer-review

Abstract

In order to enhance the extraction and identification of polysaccharides in red pine bark extract, bifunctional monomers molecularly imprinted polymer microspheres (Fe3O4@SiO2-C〖FY=,1〗C@MIPs) were prepared by using magnetic Fe3O4@SiO2-C〖FY=,1〗C functional microspheres as the carrier, 4-vinyl phenylboric acid (VPBA) and acrylamide (AM) as functional monomer, N,N'-methylene double acrylamide (MBA) as crosslinking agent and ammonium persulfate (APS) as initiator for specific adsorption of starch polysaccharides. The properties of molecularly imprinted polymeric microspheres were determined by scanning electron microscopy, transmission electron microscopy and infrared spectroscopy. The results showed that APBA was successfully grafted on the surface, and the starch adsorption amount and the imprinting factor IF reached 12.48 mg/g and 3.029, respectively. The adsorption of MIPs was more consistent with the second-order kinetic model and Langmuir adsorption curve. The covalent bond binding of boric acid derivative (APBA) and polysaccharide molecule and the hydrogen bond binding of amides compound (AMPS) and polysaccharide molecule increased the adsorption amount and specificity of molecular imprinting. Fe3O4@SiO2-C〖FY=,1〗C could specifically adsorb G10000 polysaccharide.

Translated title of the contributionPreparation and identification of vinyl functionalized magnetic molecularly imprinted polymers
Original languageChinese (Traditional)
Pages (from-to)1018-1025
Number of pages8
JournalGongneng Cailiao/Journal of Functional Materials
Volume50
Issue number1
DOIs
StatePublished - 30 Jan 2019
Externally publishedYes

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