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      KCI등재

      UV-Curable Fluorinated Crosslinkable Polyurethane-Acrylates for Marine Antifouling Coatings

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      https://www.riss.kr/link?id=A104561021

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      다국어 초록 (Multilingual Abstract)

      To prepare UV-curable polyurethane-acrylate oligomer, NCO-terminated urethane prepolymers with trimethylolpropane, [TMP; 0 (0), 0.1 (0.021) and 0.2 (0.043) mole (mole fraction)] as crosslinkable tri-functional chain extender were end-capped with penta...

      To prepare UV-curable polyurethane-acrylate oligomer, NCO-terminated urethane prepolymers with trimethylolpropane, [TMP; 0 (0), 0.1 (0.021) and 0.2 (0.043) mole (mole fraction)] as crosslinkable tri-functional chain extender were end-capped with pentaerythritol triacrylate [PETA; 2.0 (0.400), 1.7 (0.354) and 1.4 (0.304) mole (mole fraction)] with one hydroxyl group/three vinyl functionalities. The stable as-formulated UV-curable polyurethane-acrylates [stable mixtures of PETA-capped oligomer/ reactive acrylic monomer diluents without/with heptadecafluorodecyl methacrylate (PFA; 0, 6 and 9 wt%)] were formed up to 0.2 (0.043) mole (mole fraction) of TMP content in the prepolymer, while homogeneous-mixing failed at 0.3 (0.068) mole (mole fraction), in which the crosslink density in NCO-terminated urethane prepolymer was too high to enable the formation of stable mixture. This study examined the effect of TMP/PETA molar ratio and heptadecafluorodecyl methacrylate (PFA) content (wt%) on the properties of UV-cured polyurethane-acrylates as marine antifouling coating materials. The properties of UV-cured polyurethane-acrylate were found to be significantly dependent on the crosslinkable TMP/PETA ratio and PFA content. With the increasing of the TMP and PFA contents, the contact angles increased, and consequently the surface tension decreased. The adhesion of algae/barnacles to PFA contained film samples were found to be sufficiently weak to allow their easy removal. These results suggest that the UV-cured samples containing PFA have strong potential as coating materials for antifouling applications.

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      참고문헌 (Reference)

      1 Xu, H, "UV-Curable Waterborne Polyurethane-Acrylate: Preparation, Characterization" 73 : 47-53, 2016

      2 Lin, Y. H, "UV-Curable Low-Surface-Energy Fluorinated Poly(urethane-acrylate)s for Biomedical Applications" 44 : 2927-2937, 2008

      3 Hwang, H. D, "UV-Curable Low Surface Energy Fluorinated Polycarbonate-Based Polyurethane Dispersion" 362 : 274-284, 2011

      4 Canak, T. C, "Synthesis of Fluorinated Urethane Acrylate Based UV-Curable Coatings" 76 : 388-399, 2013

      5 Lai, Y. C, "Synthesis and Structure-Property Relationships of UV-Curable Urethane Prepolymers with Hard-Soft-Hard Blocks" 42 : 2039-2044, 1991

      6 Shin, M. S, "Synthesis and Properties of Waterborne Fluorinated Polyurethane-Acrylate using a Solvent-/Emulsifier-Free Method" 54 : 4873-4882, 2013

      7 Park, J. M, "Synthesis and Properties of UV-Curable Polyurethane Acrylates Containing Fluorinated Acrylic Monomer/Vinyltrimethoxysilane" 72 : 1921-1936, 2015

      8 Zhang, C, "Synthesis and Properties of PDMS Modified Waterborne Polyurethane-Acrylic Hybrid Emulsion by Solvent-Free Method" 63 : 238-244, 2008

      9 Xin, H, "Synthesis and Properties of Cationic Polyurethane-Fluorinated Acrylic Hybrid Latexes by Emulsifier-Free Emulsion Polymerization and the Solvent-Free Method" 67 : 1849-1863, 2011

      10 Tanaka, H, "Synthesis and Coating Application of Waterborne Fluoroacrylic-Polyurethane Composite Dispersion" 153 : 597-601, 1999

      1 Xu, H, "UV-Curable Waterborne Polyurethane-Acrylate: Preparation, Characterization" 73 : 47-53, 2016

      2 Lin, Y. H, "UV-Curable Low-Surface-Energy Fluorinated Poly(urethane-acrylate)s for Biomedical Applications" 44 : 2927-2937, 2008

      3 Hwang, H. D, "UV-Curable Low Surface Energy Fluorinated Polycarbonate-Based Polyurethane Dispersion" 362 : 274-284, 2011

      4 Canak, T. C, "Synthesis of Fluorinated Urethane Acrylate Based UV-Curable Coatings" 76 : 388-399, 2013

      5 Lai, Y. C, "Synthesis and Structure-Property Relationships of UV-Curable Urethane Prepolymers with Hard-Soft-Hard Blocks" 42 : 2039-2044, 1991

      6 Shin, M. S, "Synthesis and Properties of Waterborne Fluorinated Polyurethane-Acrylate using a Solvent-/Emulsifier-Free Method" 54 : 4873-4882, 2013

      7 Park, J. M, "Synthesis and Properties of UV-Curable Polyurethane Acrylates Containing Fluorinated Acrylic Monomer/Vinyltrimethoxysilane" 72 : 1921-1936, 2015

      8 Zhang, C, "Synthesis and Properties of PDMS Modified Waterborne Polyurethane-Acrylic Hybrid Emulsion by Solvent-Free Method" 63 : 238-244, 2008

      9 Xin, H, "Synthesis and Properties of Cationic Polyurethane-Fluorinated Acrylic Hybrid Latexes by Emulsifier-Free Emulsion Polymerization and the Solvent-Free Method" 67 : 1849-1863, 2011

      10 Tanaka, H, "Synthesis and Coating Application of Waterborne Fluoroacrylic-Polyurethane Composite Dispersion" 153 : 597-601, 1999

      11 Park, I. J, "Surface Properties of the Fluorine-Containing Graft Copolymer of Poly((perfluoroalkyl)ethylmethacrylate)-g-Poly(methyl methacrylate)" 31 : 7555-7558, 1998

      12 Li, H, "Surface Composition and Property of Film Prepared with Aqueous Dispersion of Polyurethaneurea-Acrylate Including Fluorinated Block Copolymer" 40 : 2195-2201, 2004

      13 Yamazaki, E, "Segmented Poly(urethane)s Synthesized Directly from Isocyanate-Terminated Prepolymers and Masked Diamines I. Quantitative Synthesis" 29 (29): 811-817, 1997

      14 Chang, W, "Role of Functionality in MDI-Based Elastomer Preparation" 51 : 1077-1085, 1994

      15 Consaga, J. P, "Propertis of Htdroxyl-Termonatied Polybutadiene-Urethane Systems" 15 : 2941-2956, 1971

      16 Jung, H. C, "Properties of Crosslinked Polyurethanes Synthesized from 4,4’-Diphenylmethane Diisocyanate and Polyester Polyol" 78 : 624-630, 2000

      17 Kothandaraman, H, "Preparation, Properties, and Crosslinking Studies on Polyurethane Elastomers" 21 (21): 829-839, 1989

      18 Park, Y. G, "Preparation and Properties of Waterborne Polyurethane/Self-Crosslinkable Fluorinated Acrylic Copolymer Hybrid Emulsions Using a Solvent/Emulsifier-Free Method" 293 : 1369-1382, 2015

      19 Jeon, J. H, "Preparation and Properties of UV-Curable Fluorinated Polyurethane Acrylates Containing Crosslinkable Vinyl Methacrylated for Antifouling Coatings" 132 : 42168-, 2015

      20 Lee, S. G, "Preparation and Properties of Emulsifier/N-methylpyttolidone-Free Crosslinkable Waterborne Polyurethane-acrylation Emulsions for Footwear Adhesives. I. Effect of the Acrylic Monomer Content" 133 : 43758-, 2016

      21 Cheon, J. M, "Preparation and Properties of Emulsifier-/NMP-Free Crosslinkable Waterborne Polyurethane- Acrylic Hybrid Emulsions for Footwear Adhesives(Ⅱ)- Effect of Dimethylol Propionic Acid (DMPA)/Pentaerylthritol Triacrylate (PETA) Content" 16 (16): 189-197, 2016

      22 Kaibin, L, "Preparation and Properties of Castor Oil/Pentaerythritol Triacrylate-Based UV Curable Waterborne Polyurethane Acrylate" 78 : 146-154, 2015

      23 Spirkova, M, "Polybutadiene-Based Polyurethanes with Controlled Properties: Preparation and Characterization" 77 : 381-389, 2000

      24 Krakovsky, I, "Inhomogeneous Structure of Polyurethane Networks Based on Poly(butadiene)diol: 1. The Effect of the Poly(butadiene)diol Content" 38 : 3637-3643, 1997

      25 K. Kroyer, "Germ. Pat. No. 2,101,074"

      26 Kano, Y, "Estimation of Surface Tension and Surface Segregtion of Poly(ethyl acrylate)/Poly(vinylidene fluoride-co-hexafluoro aceton) Blends" 37 : 4497-4503, 1996

      27 Mark, H, "Encyclopedia of Polymer Science and Technology Volume 11" John Wiley & Sons, Inc 506-563, 1972

      28 Chen, Y, "Emulsifier-Free Latex of Fluorinated Acrylate Copolymer" 42 : 694-701, 2006

      29 Chiou, B. S, "Effects of Crosslinking on Thermal and Mechanical Properties of Polyurethanes" 83 : 212-223, 2002

      30 Fan, Q, "Effects of Crosslinking Density on Structure and Properties of Interpenetrating Polymer Networks from Polyurethane and Nitroguar Gum" 29 : 758-767, 2008

      31 이성원, "Effect of Total Acrylic/Fluorinated Acrylic Monomer Contents on the Properties of Waterborne Polyurethane/Acrylic Hybrid Emulsions" 한국고분자학회 21 (21): 709-718, 2013

      32 Desai, S, "Effect of Polyols and Diisocyanaies on Thermo-Mechanical and Mophological Properties of Polyurethanes" 30 : 711-725, 2000

      33 Liu, Y, "Effect of Chemical Crosslinking on the Structure and Mechanical Properties of Polyurethane Prepared from Copoly (PPO-THF) Triols" 67 : 2163-2169, 1998

      34 Cheng, S, "Core-Shell Latex Containing Fluorinated Polymer Rich in Shell" 85 : 1147-1153, 2002

      35 Beregi, "Boat Hull Antifouling cpd, French Pat. No. 2,050,794"

      36 Kaelble, D. H, "A Surface Energy Analysis of Bioadhesion" 18 : 475-482, 1977

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-11-01 학술지명변경 한글명 : 청정기술 -> Clean Technology
      외국어명 : CLEAN TECHNOLOGY -> Clean Technology
      KCI등재
      2018-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2015-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2007-07-04 학술지명변경 한글명 : 한국청정기술학회지 -> 청정기술 KCI등재후보
      2007-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2005-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.26 0.26 0.25
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.29 0.28 0.4 0.1
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