Directed Self-Assembly in "Breath Figure" Templating of Melamine-Based Amphiphilic Copolymers: Effect of Hydrophilic End-Chain on Honeycomb Film Formation and Wetting

被引:10
|
作者
Yin, Hongyao [1 ,2 ]
Feng, Yujun [1 ]
Billon, Laurent [2 ]
机构
[1] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
[2] UPPA, CNRS UMR 5254, Inst Sci Analyt & Phys Chim Environm & Mat IPREM, Helioparc,2 Ave Angot, F-64053 Pau 9, France
关键词
amphiphiles; block copolymers; hydrogen bonds; surface chemistry; thin films; STRUCTURED POROUS FILMS; RAFT POLYMERIZATION; BLOCK-COPOLYMERS; DIBLOCK COPOLYMERS; PHASE-SEPARATION; SURFACES; WETTABILITY; FABRICATION; MEMBRANES; DISPERSION;
D O I
10.1002/chem.201704369
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amphiphilic copolymers are widely used in the fabrication of hierarchically honeycomb-structured films through a breath figure (BF) process because the hydrophilic block plays a key role in stabilising water templating. However, the hydrophilic monomers reported are mainly confined to acrylic acid and its derivatives, which largely limits understanding of the formation of BF arrays and the introduction of additional functions on porous films. The relationship between polymer composition, film microstructure and surface properties are also less documented. Herein, a novel melamine-based hydrophilic moiety, N-[3-({3-[(4,6-bis{[3-(dimethylamino)propyl]amino}-1,3,5-triazin-2yl)amino]propyl}(methyl)amino)propyl]methacrylamide (ANME), was incorporated into polystyrene (PS) chains by combining atom-transfer radical polymerisation and post-modification to afford three well-defined end-functionalised PS-PANME derivatives. These polymers were used to fabricate honeycomb films through the BF technique. Both inner and outer microstructures of the films were characterised by optical microscopy, AFM and SEM. Polymer hydrophilicity is enhanced upon increasing the PANME content, which results in variation of the film microstructure and porosity, and provokes a transition from Cassie-Baxter to Wenzel behaviour. Furthermore, the surface wettability of as-prepared honeycomb films and corresponding pillared films is mainly governed by film morphology, rather than by the properties of the polymers. Knowledge of the relationships between polymer composition and film structure, as well as surface wettability, is beneficial to design and prepare hierarchically porous films with desirable structures and properties.
引用
收藏
页码:425 / 433
页数:9
相关论文
共 5 条
  • [1] Direct formation of hydrophilic honeycomb film by self-assembly in breath figure templating of hydrophobic polylacticacid/ionic surfactant complexes
    Yin, Hongyao
    Zhan, Fuxing
    Yu, Yue
    Li, Zongcheng
    Feng, Yujun
    Billon, Laurent
    SOFT MATTER, 2019, 15 (25) : 5052 - 5059
  • [2] Hierarchically organized honeycomb films through block copolymer directed self-assembly in "breath figure" templating and soft microwave-triggered annealing
    Benoot, Nicolas
    Marcasuzaa, Pierre
    Pessoni, Laurence
    Chasvised, Sirikorn
    Reynaud, Stephanie
    Bousquet, Antoine
    Billon, Laurent
    SOFT MATTER, 2018, 14 (23) : 4874 - 4880
  • [3] Hierarchical honeycomb-structured films by directed self-assembly in "breath figure'' templating of ionizable "clicked'' PH3T-b-PMMA diblock copolymers: an ionic group/counter-ion effect on porous polymer film morphology
    Ji, Eunkyung
    Pellerin, Virginie
    Ehrenfeld, Francis
    Laffore, Anthony
    Bousquet, Antoine
    Billon, Laurent
    CHEMICAL COMMUNICATIONS, 2017, 53 (11) : 1876 - 1879
  • [4] Directed self-assembly in "breath figure" templating of block copolymers followed by soft hydrolysis-condensation: One step towards synthetic bio-inspired silica diatoms exoskeleton
    Aynard, Antoine
    Pessoni, Laurence
    Billon, Laurent
    POLYMER, 2020, 210
  • [5] Self-Assembly and Morphology Control of New L-Glutamic Acid-Based Amphiphilic Random Copolymers: Giant Vesicles, Vesicles, Spheres, and Honeycomb Film
    Zhu, Xuewang
    Liu, Minghua
    LANGMUIR, 2011, 27 (21) : 12844 - 12850