Novel methacrylate copolymers functionalized with fluoroarylamide; copolymerization kinetics, thermal stability and antimicrobial properties

被引:2
作者
Erol, Ibrahim [1 ]
Deveci, Turker [1 ]
机构
[1] Afyon Kocatepe Univ, Fac Sci & Arts, Dept Chem, TR-03200 Afyon, Turkey
关键词
Methacrylate; glycidylmethacrylate; thermal stability; monomer reactivity ratio; biological activity; MONOMER REACTIVITY RATIOS; 2,4-DICHLOROPHENYL METHACRYLATE; 2-(3-MESITYL-3-METHYLCYCLOBUTYL)-2-HYDROXYETHYL METHACRYLATE; PHOTOOXIDATIVE DEGRADATION; POLY(METHYL METHACRYLATE); METHYL-METHACRYLATE; BEHAVIOR; STYRENE; HOMOPOLYMERS; SYSTEM;
D O I
10.1080/09205063.2021.1938858
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In the first step of this study, 2-oxo-2-[(2,4,6-trifluorophenyl)amino]ethyl-2-methylprop-2-enoate(OTFAMA) monomer was synthesized and characterized. Then, a series copolymers were obtained by free-radical copolymerization method of OTFAMA and glycidyl methacrylate (GMA), which is a commercial monomer at 65 degrees C in 1,4-dioxane solvent. Structural characterizations of synthesized monomer and copolymers were carried out using FTIR, H-1-C-13-NMR instruments. The composition of the copolymers was estimated by elemental analysis. The reactivity ratios (r(1) and r(2)) were obtained from the various linear graphical methods. The values of r(1) (OTFAMA) = 0.33 and r(2) (GMA) = 0.45 were found from the same graphical methods. The thermal behaviors of all the polymers have been investigated using the differential scanning calorimetry (DSC) and the thermogravimetric analysis (TGA). A kinetic study of the thermal decompostion of copolymers was investigated using thermogravimetric analyzer with non-isothermal methods selected for analyzing solid-state kinetics data. The average activation energy values were calculated via Kissinger and Ozawa models in a period of alpha = 0.10-0.80. Photo stability of the copolymers was investigated. Also, the biological activity of the copolymers against different bacterial and fungal species has been investigated.
引用
收藏
页码:1810 / 1834
页数:25
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