Thermally mendable material based on a furyl-telechelic semicrystalline polymer and a maleimide crosslinker

详细信息    查看全文

• 作者：Le-Thu T. Nguyen ; Ha Tran Nguyen ; Thuy Thu Truong
• 关键词：Mendable polymers ; Diels ; Alder ; Thermoreversible ; Semicrystalline polymers
• 刊名：Journal of Polymer Research
• 出版年：2015
• 出版时间：September 2015
• 年：2015
• 卷：22
• 期：9
• 全文大小：3,343 KB
• 参考文献：1.Blaiszik BJ, Kramer SLB, Olugebefola SC, Moore JS, Sottos NR, White SR (2010) Self-healing polymers and composites. Annu Rev Mater Res 40:179–211CrossRef
  2.Hillewaere XKD, Teixeira RFA, Nguyen L-TT, Ramos JA, Rahier H, Du Prez FE (2014) Autonomous self-healing of epoxy thermosets with thiol-isocyanate chemistry. Adv Funct Mater 24:5575–5583CrossRef
  3.Fereidoon A, Ghorbanzadeh Ahangari M, Jahanshahi M (2013) Effect of nanoparticles on the morphology and thermal properties of self-healing poly(urea-formaldehyde) microcapsules. J Polym Res 20:1–8CrossRef
  4.Rahimi A, Amiri S (2014) Self-healing hybrid nanocomposite coatings with encapsulated organic corrosion inhibitors. J Polym Res 22:1–8
  5.Bergman SD, Wudl F (2008) Mendable polymers. J Mater Chem 18:41–62CrossRef
  6.Zhang Y, v Y-h, Zhang Z-p (2015) The influence of 2,4-toluene diisocyanate content on the intrinsic self-healing performance of polyurethane at room-temperature. J Polym Res 22:1–6CrossRef
  7.Cheng C, Bai X, Zhang X, Li H, Huang Q, Tu Y (2015) Self-healing polymers based on a photo-active reversible addition-fragmentation chain transfer (RAFT) agent. J Polym Res 22:1–8CrossRef
  8.Zhang MQ, Rong MZ (2013) Intrinsic self-healing of covalent polymers through bond reconnection towards strength restoration. Polym Chem 4:4878–4884CrossRef
  9.Liu Y-L, Chuo T-W (2013) Self-healing polymers based on thermally reversible Diels-Alder chemistry. Polym Chem 4:2194–2205CrossRef
  10.Mignard N, Okhay N, Jegat C, Taha M (2013) Facile elaboration of polymethylmethacrylate / polyurethane interpenetrating networks using Diels-Alder reactions. J Polym Res 20:1–13CrossRef
  11.Chen X, Dam MA, Ono K, Mal A, Shen H, Nutt SR, Sheran K, Wudl F (2002) A thermally re-mendable cross-linked polymeric material. Science 295:1698–1702CrossRef
  12.Tasdelen MA (2011) Diels-Alder “click” reactions: recent applications in polymer and material science. Polym Chem 2:2133–2145CrossRef
  13.Tian Q, Yuan YC, Rong MZ, Zhang MQ (2009) A thermally remendable epoxy resin. J Mater Chem 19:1289–1296CrossRef
  14.Zhang Y, Broekhuis AA, Picchioni F (2009) Thermally self-healing polymeric materials: the next step to recycling thermoset polymers? Macromolecules 42:1906–1912CrossRef
  15.Kavitha AA, Singha NK (2009) “Click chemistry” in tailor-made polymethacrylates bearing reactive furfuryl functionality: a new class of self-healing polymeric material. ACS Appl Mater Interfaces 1:1427–1436CrossRef
  16.Scheltjens G, Diaz MM, Brancart J, Assche GV, Mele BV (2013) A self-healing polymer network based on reversible covalent bonding. React Funct Polym 73:413–420CrossRef
  17.Bose RK, Kötteritzsch J, Garcia SJ, Hager MD, Schubert US, van der Zwaag S (2014) A rheological and spectroscopic study on the kinetics of self-healing in a single-component diels–alder copolymer and its underlying chemical reaction. J Polym Sci Part A Polym Chem 52:1669–1675CrossRef
  18.Lendlein A, Sauter T (2013) Shape-memory effect in polymers. Macromol Chem Phys 214:1175–1177CrossRef
  19.Lendlein A, Kelch S (2002) Shape-memory polymers. Angew Chem Int Ed 41:2034–2057CrossRef
  20.Lendlein A, Behl M, Hiebl B, Wischke C (2010) Shape-memory polymers as a technology platform for biomedical applications. Expert Rev Med Devices 7:357–379CrossRef
  21.Leng J, Lan X, Liu Y, Du S (2011) Shape-memory polymers and their composites: stimulus methods and applications. Prog Mater Sci 56:1077–1135CrossRef
  22.Xu H, Yu C, Wang S, Malyarchuk V, Xie T, Rogers JA (2013) Deformable, programmable, and shape-memorizing micro-optics. Adv Funct Mater 23:3299–3306CrossRef
  23.Behl M, Razzaq MY, Lendlein A (2010) Multifunctional shape-memory polymers. Adv Mater 22:3388–3410CrossRef
  24.Kirkby EL, Rule JD, Michaud VJ, Sottos NR, White SR, Månson J-AE (2008) Embedded shape-memory alloy wires for improved performance of self-healing polymers. Adv Funct Mater 18:2253–2260CrossRef
  25.Kirkby EL, Michaud VJ, Månson JAE, Sottos NR, White SR (2009) Performance of self-healing epoxy with microencapsulated healing agent and shape memory alloy wires. Polymer 50:5533–5538CrossRef
  26.Li G, Zhang P (2013) A self-healing particulate composite reinforced with strain hardened short shape memory polymer fibers. Polymer 54:5075–5086CrossRef
  27.Li G, Ajisafe O, Meng H (2013) Effect of strain hardening of shape memory polymer fibers on healing efficiency of thermosetting polymer composites. Polymer 54:920–928CrossRef
  28.Rodriguez ED, Luo X, Mather PT (2011) Linear/network poly(ε-caprolactone) blends exhibiting Shape Memory Assisted Self-Healing (SMASH). ACS Appl Mater Interfaces 3:152–161CrossRef
  29.Luo X, Mather PT (2013) Shape memory assisted self-healing coating. ACS Macro Lett 2:152–156CrossRef
  30.García-Huete N, Laza J, Cuevas J, Gonzalo B, Vilas J, León L (2014) Shape memory effect for recovering surface damages on polymer substrates. J Polym Res 21:1–10CrossRef
  31.Zhang J, Niu Y, Huang C, Xiao L, Chen Z, Yang K, Wang Y (2012) Self-healable and recyclable triple-shape PPDO-PTMEG co-network constructed through thermoreversible Diels-Alder reaction. Polym Chem 3:1390–1393CrossRef
  32.Rivero G, Nguyen L-TT, Hillewaere XKD, Du Prez FE (2014) One-Pot thermo-remendable shape memory polyurethanes. Macromolecules 47:2010–2018CrossRef
  33.Lu X, Fei G, Xia H, Zhao Y (2014) Ultrasound healable shape memory dynamic polymers. J Mater Chem A 2:16051–16060CrossRef
  34.Heo Y, Sodano HA (2014) Self-healing polyurethanes with shape recovery. Adv Funct Mater 24:5261–5268CrossRef
  35.Woodruff MA, Hutmacher DW (2010) The return of a forgotten polymer—Polycaprolactone in the 21st century. Prog Polym Sci 35:1217–1256CrossRef
  36.Narita M, Teramoto T, Okawara M (1971) Syntheses and reactions of functional polymers. LIV. Syntheses and polymerizations of O-substituted-N-hydroxymaleimides. Bull Chem Soc Jpn 44:1084–1089CrossRef
  37.Nguyen L-TT, Gokmen MT, Du Prez FE (2013) Kinetic comparison of 13 homogeneous thiol-X reactions. Polym Chem 4:5527–5536CrossRef
  38.Mellouki A, Herman M, Demaison J, Lemoine B, Margulès L (1999) Rotational analysis of the ν7 band in furan (C4H4O). J Mol Spectrosc 198:348–357CrossRef
  39.Mani R, Bhattacharya M (2001) Properties of injection moulded blends of starch and modified biodegradable polyesters. Eur Polym J 37:515–526CrossRef
  
• 作者单位：Le-Thu T. Nguyen (1)
  Ha Tran Nguyen (1) (2)
  Thuy Thu Truong (1)
  
  1. Faculty of Materials Technology, Ho Chi Minh City University of Technology, Vietnam National University, 268 Ly Thuong Kiet, District 10, Ho Chi Minh City, Vietnam
  2. Materials Technology Key Laboratory (Mtlab), Ho Chi Minh City University of Technology, Vietnam National University, Ho Chi Minh City, Vietnam
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Polymer Sciences
  Industrial Chemistry and Chemical Engineering
  Characterization and Evaluation Materials
  
• 出版者：Springer Netherlands
• ISSN：1572-8935

文摘

Based on Diels-Alder reaction, a furyl-telechelic semicrystalline polycaprolactone was crosslinked by a tris-maleimide crosslinker. The synthesized precursors and network were fully characterized via proton nuclear magnetic resonance (1H NMR) and Fourier transform infrared (FT-IR) spectroscopies, gel permeation chromatography (GPC), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and wide-angle powder X-ray diffraction (XRD) measurements. The obtained material showed mendability of scratches under thermal treatment, as evidenced by optical microscopy and tensile analysis. The mending process was a combination of the shape recovery effect favoring scratch closure and the re-crosslinking of the cleaved Diels-Alder bonds at temperatures slightly above the melting transition of polycaprolactone chains. A scratch healing efficiency determined by tensile tests of about 70 % was achieved.