• Title/Summary/Keyword: fluorinated alkyl acrylate

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Synthesis and Characterization of Polyacrylate Derivatives Baying Protected Isocyanate Groups and fluorinated Alkyl Groups (보호된 이소시아네이트기와 불소화 알킬기를 가지는 아크릴계 고분자의 합성과 특성)

  • 김우식;김민우;정은천;백창훈;박이순;강인규;박수영
    • Polymer(Korea)
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    • v.27 no.4
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    • pp.364-369
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    • 2003
  • The copolymerizations of 2-fluorohexylethyl acrylate (FA) with 2-(o-(1'-methylpropylidenamino)carboxyl amino)ethyl methacrylate(MEM) with different molar ratios of the two monomers were carried out in methyl ethyl ketone using ${\alpha}$,${\alpha}$'-azobisisobutyronitrile as an initiator to synthesize water repellent polyacrylate derivatives with protected isocyanate groups. The contents of FA and MEM in the copolymers were analyzed by NMR. The monomer reactivity ratios of MEM (1) and FA (2) were determined by Kelen-Tudos plot as follows : r$\_$1/=1.59 and r$\_$2/=0.50. The number-average molecular weights of the copolymers were in the range of 39400 to 72400 and the polydispersity indexes were about 1.5. The protected isocyanate groups in the copolymers were converted into isocyanate groups above 150$^{\circ}C$. The contact angle of the copolymer with 65 ㏖% of FA fur water was about 95$^{\circ}$.

Synthesis and Water Repellency of Polymers with Fluorinated Alkyl Group and Isocyanate Group (불소화 알킬기와 이소시아네이트기를 가지는 고분자의 합성과 발수성)

  • Baek Chang-Hoon;Kong Jong-Yun;Hyun Seok-Hee;Lim Yong-Jin;Kim Woo-Sik
    • Polymer(Korea)
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    • v.29 no.5
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    • pp.433-439
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    • 2005
  • The copolymers were prepared by the emulsion copolymerization of fluoroalky lacrylate-stearylacrylate-m-isopropenyl-${\alpha},\;{\alpha}'$-dimethylbenzyl isocyanate (TMI) in order to obtain water repellent polymers. The respective copolymerization rates of the three monomers considerably depended upon the use of the nonionic emulsifier and the nonionic-cationic mixed emusifier, and the optimum conditions were obtained. The particle sizes of the copolymers were in the range of 105 to 222nm. The particle sizes of the copolymers prepared by the use of the mixed emulsifiers were smaller than those of the copolymers prepared by the use of the nonionic emulsifier. The reactions of both TMI-N-methyl acetamide and TMI-cellobiose did not take place. However, the reaction of TMI-n-butylamine occurred. The water contact angles before and after washing three times for nylon and poly(ethylene terephthalate) (PET) fabrics coated with the copolymer prepared by the use of mixed emulsifier were about $139^{\circ}\;and\;133^{\circ}$ Therefore, the copolymer showed good durable repellency for nylon and PET.