Hydrophobic-oleophobic polyurethane with mechanical reinforcement: Synthesized by thiol-ene click chemistry

被引:3
|
作者
Li, Yuhan [1 ]
Liu, Ziyu [1 ]
Liu, Xiaoran [1 ]
Gao, Feng [1 ]
Cheng, Jue [1 ]
Zhang, Junying [1 ]
机构
[1] Beijing Univ Chem Technol, Key Lab Carbon Fiber & Funct Polymers, Minist Educ, Beijing 100029, Peoples R China
关键词
Hydrophobic-oleophobic; Thiol-ene click chemistry; Mechanical reinforcement; FLUORINATED POLYURETHANE; FUNCTIONALIZATION; PARAMETERS;
D O I
10.1016/j.eurpolymj.2023.112574
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polyurethane (PU) is a universal polymer material with excellent performance, widely used as foam materials, adhesives, coatings, rubber, etc. Nevertheless, the considerable presence of ester and ether bonds in the polyurethane backbone, combined with the hydrophilic -OH group located at the end of molecular chain, renders it intrinsically hydrophilic. This inherent hydrophilicity presents substantial constraints on its potential utilization in flexible electronic displays, wearable electronic devices, and various other fields. It is a great challenge for hydrophobic polyurethane to simultaneously achieve mechanical reinforcement. Herein, the fluorinated chain extenders were introduced into PU, which not only resulted in low surface energy but also improved the surface roughness through the microphase separation due to the difference in the solubility parameters between the fluorine-containing side chain and the main chain. The long-chain perfluorinated extender was achieved via thiol-ene click chemistry, thus regulating the fluorine content by adjusting the amount of chain extender. The low surface energy and high roughness, developed by microphase separation, make the DFX-PU films exhibit excellent hydrophobicity (120 degrees) and oleophobicity (121 degrees). Additionally, the fluorine-containing side chains aggregate to form physical cross-linking points, reinforcing the mechanical properties of the film. When the fluorine-containing chain extender accounted for 10% (DF0.5-PU), the PU film showed the best mechanical properties. Compared with the control group, tensile strength is enhanced by 165%, the toughness is increased by 287%, and the elongation-at-break was improved by 156%.
引用
下载
收藏
页数:9
相关论文
共 50 条
  • [21] Photochemical Microcontact Printing by Thiol-Ene and Thiol-Yne Click Chemistry
    Wendeln, Christian
    Rinnen, Stefan
    Schulz, Christian
    Arlinghaus, Heinrich F.
    Ravoo, Bart Jan
    LANGMUIR, 2010, 26 (20) : 15966 - 15971
  • [22] Supramolecular polymers synthesized by thiol-ene click polymerization from supramonomer
    Song, Qiao
    Li, Fei
    Yang, Liulin
    Wang, Zhiqiang
    Zhang, Xi
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2015, 249
  • [23] Application of Thiol-ene "click" Chemistry to Preparation of Hyperbranched Polyurethane Acrylate Oligomers Containing Carboxyl Groups
    Han, Wensong
    JOURNAL OF PHOTOPOLYMER SCIENCE AND TECHNOLOGY, 2015, 28 (03) : 419 - 427
  • [24] Supramolecular polymers synthesized by thiol-ene click polymerization from supramonomers
    Song, Qiao
    Li, Fei
    Yang, Liulin
    Wang, Zhiqiang
    Zhang, Xi
    POLYMER CHEMISTRY, 2015, 6 (03) : 369 - 372
  • [25] Preparation and properties of catechol-based waterborne polyurethane based on thiol-ene click chemistry reaction
    Ren Longfang
    Lin Congcong
    Lei Pingchuan
    PROGRESS IN ORGANIC COATINGS, 2021, 157 (157)
  • [26] Silicon-thioether dendrimers synthesized with thiol-ene chemistry
    Rissing, Christiana J.
    Son, David Y.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2009, 237
  • [27] Immobilization of Enzymes via Microcontact Printing and Thiol-Ene Click Chemistry
    Buhl, Moritz
    Vonhoeren, Benjamin
    Ravoo, Bart Jan
    BIOCONJUGATE CHEMISTRY, 2015, 26 (06) : 1017 - 1020
  • [28] Versatile functionalization of aromatic polysulfones via thiol-ene click chemistry
    Park, Eun Joo
    Lee, Woo-Hyung
    Bae, Chulsung
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2016, 54 (19) : 3237 - 3243
  • [29] Modification of the surface tension of cellulosic substrates by thiol-ene click chemistry
    Green, Andrea
    Ozer, Ruya R.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 241
  • [30] The Emergence of Thiol-Ene Coupling as a Click Process for Materials and Bioorganic Chemistry
    Dondoni, Alessandro
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2008, 47 (47) : 8995 - 8997