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Preparation of Poly(ethylene-co-acrylic acid) Grafted with Aliphatic Quaternary Ammonium Salts as Antibacterial Polymers

Authors
Noh, HongcheYu, Ji-SooKo, JongSungKim, Joung MinOh, Seong-Geun
Issue Date
Aug-2017
Publisher
WILEY-V C H VERLAG GMBH
Keywords
Antibacterial polymer; Steglich esterification; Quaternary ammoniums salts; Poly(ethylene-co-acrylic acid) copolymer; Thermal decomposition; Grafting; Electrospinning
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.38, no.8, pp.890 - 898
Indexed
SCIE
SCOPUS
KCI
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
38
Number
8
Start Page
890
End Page
898
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/151870
DOI
10.1002/bkcs.11198
ISSN
0253-2964
Abstract
To improve the antibacterial performance of poly(ethylene-co-acrylic acid) (PEAA) copolymer, aliphatic quaternary ammonium salts (QASs) was grafted into PEAA copolymers via a Steglich esterification reaction using N, N'-dicyclohexylcarbodiimide (DCC) as a dehydrating agent. The polymers were synthesized using dodecyl dimethyl hydroxyethyl ammonium chloride (DDHAC), which was prepared by quaternization of dimethylethanolamine (DMEA) with 1-chlorododecane. These polymers effectively inhibited the growth of microorganisms due to their hydrophobic chains, which were bound to PEAA copolymers. The obtained PEAA-g-DDHAC (PGD) was investigated by attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR), proton nuclear magnetic resonance (H-1 NMR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and antibacterial tests. The results showed that the antibacterial effects of PGDs were significantly improved by alkyl grafting, and this improvement depended on reaction temperature. The highest antibacterial activity was observed for polymers synthesized at 135 degrees C against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli. Their decomposition rate was accelerated as the temperature increased above 165 degrees C because of the thermal decomposition of DDHAC.
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