Preparation of monodisperse functional poly(styrene-co-acrylamidoxime) microsphere with chelating amidoxime group

Ching Wen Chen, Chuh Yung Chen, Zong Huei Cioul

研究成果: Article

8 引文 (Scopus)

摘要

Monodisperse poly(styrene-co-acrylonitrile) microspheres were prepared by dispersion copolymerization of styrene (St) and acrylonitrile (AN) in ethanol (EtOH)/isopropanol medium. 2,2′-Azobis(isobutyronitrile) (AIBN) and poly(acrylic acid) (PAA) were utilized as initiator and steric stabilizer, respectively. The effects of PAA stabilizer, AIBN initiator, St/AN monomer ratio, and EtOH solvent on particle size and size distribution were investigated systematically. AN is a co-monomer with desired nitrile group (-CN); the functional P(St-co-acrylamidoxime) microsphere with chelating amidoxime group (-C(NH2)=NOH) was derived by amidoximizing the nitrile group with hydroxylamine. The percentage of chemical modification was calculated to be 51.2% in this study.

原文English
頁(從 - 到)665-672
頁數8
期刊Colloid and Polymer Science
288
發行號6
DOIs
出版狀態Published - 2010 四月 1

指紋

Acrylonitrile
Styrene
acrylonitriles
carbopol 940
Chelation
Microspheres
polystyrene
styrenes
Nitriles
preparation
nitriles
acrylic acid
initiators
Acrylics
monomers
Monomers
Hydroxylamine
2-Propanol
Acids
Chemical modification

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Polymers and Plastics
  • Colloid and Surface Chemistry
  • Materials Chemistry

引用此文

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abstract = "Monodisperse poly(styrene-co-acrylonitrile) microspheres were prepared by dispersion copolymerization of styrene (St) and acrylonitrile (AN) in ethanol (EtOH)/isopropanol medium. 2,2′-Azobis(isobutyronitrile) (AIBN) and poly(acrylic acid) (PAA) were utilized as initiator and steric stabilizer, respectively. The effects of PAA stabilizer, AIBN initiator, St/AN monomer ratio, and EtOH solvent on particle size and size distribution were investigated systematically. AN is a co-monomer with desired nitrile group (-CN); the functional P(St-co-acrylamidoxime) microsphere with chelating amidoxime group (-C(NH2)=NOH) was derived by amidoximizing the nitrile group with hydroxylamine. The percentage of chemical modification was calculated to be 51.2{\%} in this study.",
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Preparation of monodisperse functional poly(styrene-co-acrylamidoxime) microsphere with chelating amidoxime group. / Chen, Ching Wen; Chen, Chuh Yung; Cioul, Zong Huei.

於: Colloid and Polymer Science, 卷 288, 編號 6, 01.04.2010, p. 665-672.

研究成果: Article

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T1 - Preparation of monodisperse functional poly(styrene-co-acrylamidoxime) microsphere with chelating amidoxime group

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AU - Chen, Chuh Yung

AU - Cioul, Zong Huei

PY - 2010/4/1

Y1 - 2010/4/1

N2 - Monodisperse poly(styrene-co-acrylonitrile) microspheres were prepared by dispersion copolymerization of styrene (St) and acrylonitrile (AN) in ethanol (EtOH)/isopropanol medium. 2,2′-Azobis(isobutyronitrile) (AIBN) and poly(acrylic acid) (PAA) were utilized as initiator and steric stabilizer, respectively. The effects of PAA stabilizer, AIBN initiator, St/AN monomer ratio, and EtOH solvent on particle size and size distribution were investigated systematically. AN is a co-monomer with desired nitrile group (-CN); the functional P(St-co-acrylamidoxime) microsphere with chelating amidoxime group (-C(NH2)=NOH) was derived by amidoximizing the nitrile group with hydroxylamine. The percentage of chemical modification was calculated to be 51.2% in this study.

AB - Monodisperse poly(styrene-co-acrylonitrile) microspheres were prepared by dispersion copolymerization of styrene (St) and acrylonitrile (AN) in ethanol (EtOH)/isopropanol medium. 2,2′-Azobis(isobutyronitrile) (AIBN) and poly(acrylic acid) (PAA) were utilized as initiator and steric stabilizer, respectively. The effects of PAA stabilizer, AIBN initiator, St/AN monomer ratio, and EtOH solvent on particle size and size distribution were investigated systematically. AN is a co-monomer with desired nitrile group (-CN); the functional P(St-co-acrylamidoxime) microsphere with chelating amidoxime group (-C(NH2)=NOH) was derived by amidoximizing the nitrile group with hydroxylamine. The percentage of chemical modification was calculated to be 51.2% in this study.

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