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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2015 ·Vol. 54 ·期 3 ·368-380 · IF 3.113

Hyperbranched block copolymer from AB2 macromonomer: Synthesis and its reaction-induced microphase separation in epoxy thermosets

Jingang Li,Yixin Xiang,Sixun Zheng

In this contribution, we reported the synthesis of a hyperbranched block copolymer composed of poly(ε-caprolactone) (PCL) and polystyrene (PS) subchains. Toward this end, we first synthesized an α-alkynyl- and ω,ω′-diazido-terminated PCL- b -(PS) 2 macromonomer via the combination of ring-opening polymerization and atom transfer radical polymerization. By the use of this AB 2 macromonomer, the hyperbranched block copolymer ( h -[PCL- b -(PS) 2 ]) was synthesized via a copper-catalyzed Huisgen 1,3-dipolar cycloaddition (i.e., click reaction) polymerization. The hyperbranched block copolymer was characterized by means of 1 H nuclear magnetic resonance spectroscopy and gel permeation chromatography. Both differential scanning calorimetry and atomic force microscopy showed that the hyperbranched block copolymer was microphase-separated in bulk. While this hyperbranched block copolymer was incorporated into epoxy, the nanostructured thermosets were successfully obtained; the formation of the nanophases in epoxy followed reaction-induced microphase separation mechanism as evidenced by atomic force microscopy, small angle X-ray scattering, and dynamic mechanical thermal analysis. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54 , 368–380

研究领域: 高分子化学 · 材料科学 · 纳米结构功能材料 · 聚合物自组装 · 热固性树脂改性
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PROGRESS IN ORGANIC COATINGS · 2022 · IF 6.206

Design and synthesis of robust superhydrophobic coating based on epoxy resin and polydimethylsiloxane interpenetrated polymer network

Shuming Liu,Shuqi Liu,Qian Wang,Zhou Zuo,Xidong Liang

Superhydrophobic surfaces, such as lotus leaves, have attracted significant attention because of their excellent performance and potential application value. However, the micro-nano hierarchy on superhydrophobic surfaces is often vulnerable and easily broken from mechanical stress or chemical corrosion, which greatly inhibits its practical application and long-term service. This study presents a low-cost and scalable superhydrophobic coating based on an interpenetrated polymer network of polydimethylsiloxane (PDMS) and epoxy resin . The composite polymer matrix exhibits mechanical robustness as derived from the epoxy resin and low surface energy as derived from the PDMS. The superhydrophobic coating is obtained by dispersing fluoroalkyl-silane-modified SiO 2 in the solution containing the composite polymer . The multi-level hierarchical structure of SiO 2 aggregations and their strong bonding with the composite polymer gives the coating outstanding mechanical durability while maintaining superhydrophobicity after multiple cycles of sandpaper abrasion, tape peeling, and water impact tests. The chemical inertness of all components ensures its chemical stability, and the surface shows super repellency to strong acids and alkaline liquids (pH = 0–14). The coating also has excellent self-cleaning properties, which has potential applications in various industrial fields.

研究领域: 材料科学 · 高分子化学 · 表面工程 · 涂层技术 · 功能材料
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IONICS · 2016 ·Vol. 23 ·期 10 ·2603-2611 · IF 2.119

Hybrid solid electrolytes with excellent electrochemical properties and their applications in all-solid-state cells

Chen Shaojie,Zhao Yanran,Yang Jing,Yao Lili,Xu Xiaoxiong

Three types of inorganic electrolytes [Li 10 GeP 2 S 12 (LGPS), 75Li 2 S·24P 2 S 5 ·1P 2 O 5 (LPOS), Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 (LAGP)] with different particle sizes and electrochemical properties are selected as active fillers incorporated into poly(ethylene oxide) (PEO) matrix to fabricate hybrid solid electrolytes. The optimum composition of each filler is found in consideration of ionic conductivity. Their electrochemical characteristics are investigated. The optimal conductivities are 1.60 × 10 −5 , 1.18 × 10 −5 , and 2.12 × 10 −5  S cm −1 at room temperature for PEO-1%LGPS, PEO-1%LPOS, and PEO-20%LAGP, respectively. The electrochemical stability windows of these hybrid solid electrolytes are all above 5 V (vs. Li + /Li). The results show that these fillers have positive effects on the ionic conductivity, lithium ion transference number, and electrochemical stability. The relationship between the type of filler and electrochemical properties has been investigated. All-solid-state cells LiFePO 4 /Li are fabricated and present fascinating electrochemical performance with high capacity retention and good cycling stability. This work provides promising electrolytes prepared by a simple method.

研究领域: 材料科学 · 电化学 · 能源存储 · 固态离子学 · 功能材料 · 锂电池技术
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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Dramatic toughness enhancement of benzoxazine/epoxy thermosets with a novel hyperbranched polymeric ionic liquid

Shiyuan Chen,Junheng Zhang,Jiliang Zhou,Daohong Zhang,Aiqing Zhang

A novel hyperbranched polymeric ionic liquid (HBP-AMIM + PF6 − ) was explored via a thiol-ene click reaction using thiol-ended hyperbranched polyesters (THBP) and 1-allyl-3-imethylimidazolium hexafluorophosphate (AMIMPF6). The effects of HBP-AMIM + PF6 − on the curing behavior, mechanical properties and thermal stability of benzoxazine/epoxy thermosets were investigated. The gelation time and differential scanning calorimetry of non-isothermal analysis indicated that the addition of HBP-AMIM + PF6 − significantly decreased the curing temperature of benzoxazine/epoxy thermosets. Simultaneously, the addition of HBP-AMIM + PF6 − also improved the strength, toghness and thermal properties of benzoxazine-epoxy thermosets. The addition of 3 wt% HBP-AMIM + PF6 − -2 could significantly improve the mechanical and thermal performance of thermosets compared with that of cured neat benzoxazine/epoxy resin. The tensile strength, tensile toughness, flexural strength and flexural modulus, impact strength of the thermosets were improved by about 76.6%, 279.3%, 57.8%, 22.3% and 80.4%, respectively, compared with those of cured neat resin. The toughening mechanisms was attributed to the “in situ” reinforcing and toughening mechanism.

研究领域: 高分子材料 · 材料科学 · 热固性树脂 · 复合材料 · 高分子化学 · 功能材料
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2015 ·Vol. 27 ·期 4 ·3549-3556 · IF 1.569

The electrochromic properties of mesoporous WO3–polythiophene film devices with composite electrolytes

Wang Lu,Yang Zhouyong,Ni Xiuyuan

We prepare the mesoporous polythiophene–WO 3 film through in situ polymerization which is initiated by WO 3 , and fabricate the electrochromic device with the composite film. The influences of the electrolyte ions, film morphologies and counter electrode on the electrochromism of the devices are explored by UV–Vis transmittance spectra and cyclic voltammetry tests. With the aim to enhance the contrast optical transmittance, we develop the binary composite electrolytes of LiClO 4 and N(C 4 H 9 ) 4 ClO 4 solution which can promote intercalation/deintercalation process. Besides that, we use polyethylene oxide as pore-forming agent on the polythiophene–WO 3 films, so that it will be easier for electrolyte ions to diffuse in the porous film. A NiO layer also has a complementary effect on the cathodic coloration films and increases the contrast optical transmittance remarkably. Equipped with the binary electrolyte and the NiO layer as the counter electrode, the film device exhibits high performance with the contrast optical transmittance (ΔT) of 62 % and the coloration efficiency of 212.6 cm 2 /C.

研究领域: 材料科学 · 电化学 · 功能材料 · 纳米材料 · 能源材料 · 表面科学
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