Dual-stage thermosetting photopolymers for advanced manufacturing

被引:27
作者
Zhang, Biao [1 ,2 ,3 ]
Serjouei, Ahmad [4 ]
Zhang, Yuan-Fang [5 ]
Wu, Jumiati [5 ,6 ]
Li, Honggeng [5 ]
Wang, Dong [7 ]
Low, Hong Yee [5 ,6 ]
Ge, Qi [3 ]
机构
[1] Northwestern Polytech Univ, Res & Dev Inst Northwestern Polytech Univ Shenzhe, Xian Inst Flexible Elect IFE, 127 West Youyi Rd, Xian 710072, Peoples R China
[2] Northwestern Polytech Univ, Xian Inst Biomed Mat & Engn IBME, 127 West Youyi Rd, Xian 710072, Peoples R China
[3] Southern Univ Sci & Technol, Dept Mech & Energy Engn, Shenzhen 518055, Peoples R China
[4] Nottingham Trent Univ, Sch Sci & Technol, Dept Engn, Nottingham NG11 8NS, England
[5] Singapore Univ Technol & Design, Digital Mfg & Design Ctr, Singapore 487372, Singapore
[6] Singapore Univ Technol & Design, Div Engn Prod Dev, Singapore 487372, Singapore
[7] Shanghai Jiao Tong Univ, Robot Inst, Sch Mech Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Dual-stage; Crosslinked photopolymers; Advanced manufacturing; Programmable microstructures; Superhydrophobic; GLASS-TRANSITION TEMPERATURE; COMPOSITES; POLYMERIZATION; HYDROGELS; COATINGS; DESIGN; SYSTEM;
D O I
10.1016/j.cej.2021.128466
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We report a dual-stage photocrosslinked polymer network based on sequential ultraviolet (UV)-triggered radical polymerization and thermally activated etherification, applicable to the fabrication of tailorable and programmable high-resolution structures. The first stage involves photoinitiated polymerization of monomer and crosslinker to obtain an intermediate polymer network. As such, sophisticated two-dimensional (2D) and micro-scale three-dimensional (3D) structures can be made by using UV-based advanced manufacturing technologies. These complex structures can then be readily programmed into other desired, permanent shapes, in the second stage, via thermally triggered etherification which results in a highly crosslinked, robust polymer network. The intermediate network (Stage I) is characterized to have a Young's modulus ranging from 342 to 1146 MPa and a glass transition temperature from 52 degrees C to 83 degrees C, depending on the concentration of crosslinker. The same material attains a glass transition temperature ranging from 67 degrees C to similar to 105 degrees C and a Young's modulus of up to 1607 MPa after the subsequent heating process (Stage II). Originally 3D printed 2D structures can be further programmed into rigid, permanent 2.5/3D ones. Micropatterns fabricated from intrinsically hydrophilic dual stage crosslinked photopolymers through soft lithography show superhydrophobicity, and can subsequently be molded with different curvatures for practical applications.
引用
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页数:9
相关论文
共 60 条
  • [1] Photopolymerization kinetics of multifunctional monomers
    Andrzejewska, E
    [J]. PROGRESS IN POLYMER SCIENCE, 2001, 26 (04) : 605 - 665
  • [2] Anseth KS, 1995, ADV POLYM SCI, V122, P177
  • [3] Cross-Linked Solid Polymer Electrolyte for All-Solid-State Rechargeable Lithium Batteries
    Ben Youcef, Hicham
    Garcia-Calvo, Oihane
    Lago, Nerea
    Devaraj, Shanmukaraj
    Armand, Michel
    [J]. ELECTROCHIMICA ACTA, 2016, 220 : 587 - 594
  • [4] Photochemically Driven Polymeric Network Formation: Synthesis and Applications
    Blasco, Eva
    Wegener, Martin
    Barner-Kowollik, Christopher
    [J]. ADVANCED MATERIALS, 2017, 29 (15)
  • [5] Campo EA, 2008, PDL HANDB SER, P103, DOI 10.1016/B978-081551551-7.50005-X
  • [7] 3D Printing of a Dual-Curing Resin with Cationic Curable Vegetable Oil
    Cui, Yanyan
    Yang, Junlai
    Lei, Dehua
    Su, Jiahui
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2020, 59 (25) : 11381 - 11388
  • [8] Cushen J., 2016, EPOXY DUAL CURE RESI
  • [9] High bio-based content waterborne UV-curable coatings with excellent adhesion and flexibility
    Dai, Jinyue
    Ma, Songqi
    Wu, Yonggang
    Zhu, Jin
    Liu, Xiaoqing
    [J]. PROGRESS IN ORGANIC COATINGS, 2015, 87 : 197 - 203
  • [10] Photoinitiated crosslinking polymerisation
    Decker, C
    [J]. PROGRESS IN POLYMER SCIENCE, 1996, 21 (04) : 593 - 650