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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Property control of graphene aerogels by in situ growth of silicone polymer

Shuai Zhou,Xiang Zhou,Gazi Hao,Wei Jiang,Tianhe Wang

Modulation of the density (from 3.5 to 64 mg cm −3 ), hydrophobicity and oil-uptake capability of graphene aerogels in extensive ranges were achieved by reacting (3-Mercaptopropyl)trimethoxysilane (MPS) with graphene oxide solutions under heating. The reaction allowed a characteristic silicone substructure to be formed on graphene and joint the graphene layers firmly together. With the increase of MPS concentrations (≤ca. 0.2 vol%), the nano silicone polymer grown on graphene functioned as a “linker” and “spacer”, leading to a substantial decrease of the aerogel density. Because of the formation of silicone polymer and the characteristic nano-micro substructures on the backbones of graphene aerogels, the graphene aerogels exhibited a high hydrophobicity with the water contact angle consistently exceeding 142 degrees. Functionalized graphene aerogels with a density of 3.5 mg cm −3 were conveniently fabricated that displayed an extraordinary oil absorption capacity, 182 times for lubricating oil and 143 times for n-hexane of its own weight. Furthermore, the aerogels maintained their ultra-high absorption capability even after 20 absorption-distillation cycles, due to structural integrity held by the strong interfacial adhesion between graphene sheets and polymer chains of aerogels. This study offers a promising graphene aerogels and also provides a strategy for fabricating extra low dense functional materials.

研究领域: 材料科学 · 纳米科技 · 高分子化学 · 环境功能材料 · 表面与界面工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2018 ·Vol. 135 ·期 32 ·46579 · IF 1.901

Underwater polyurethane adhesive with enhanced cohesion by postcrosslinking of glycerol monomethacrylate

Xie Li,Wei Li,Zhiqing Liu,Xiaolin Wang,Heling Guo,Rongjie Wang,Xuhong Guo,Cuihua Li,Xin Jia

Polyurethane (PU) has been widely used as a glue in various areas. However, adhesion in the presence of water is greatly impeded and results in most synthetic adhesive failure. In this study, we designed and synthesized a novel PU construction; underwater PU adhesives were created by the incorporation of synthetic glycerol monomethacrylate (GMA). Furthermore, the urethane structure helped the adhesive eliminate the interfacial water barrier through interactions that were stronger than hydrogen bonding, and GMA as a crosslinking agent was used to generate post-covalent-crosslinking networks through radical polymerization. This enhanced the cohesion so the diffusion of water molecules could be overcome. Fourier transform infrared spectroscopy, thermogravimetric analysis, underwater adhesion measurements, and tensile tests were used to characterize the chemical and mechanical properties of the as-obtained adhesive. This led to an adhesive with a better mechanical strength and interfacial adhesion in water, and the results show that the mechanical properties (tensile strength, Young's modulus, and tensile elongation) of the GMA–PU adhesive were higher than those of the pure PU. As for the 4% GMA, the tensile strength was enhanced by 24.3% and the elongation was enhanced by 125.23% over those of the pure PU. This confirmed that the incorporation of GMA into the PU matrix indeed induced increasing cohesion, and the sample's adhesive strength was 21.19 ± 3.9 MPa; this indicated a superior adhesive strength over that of the pure PU. In addition, we can foresee that underwater adhesion will play an important role in prospective surgery and engineering areas. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 46579.

研究领域: 高分子材料 · 生物医学工程 · 粘附科学 · 组织工程 · 医用胶粘剂
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COMPOSITES PART A-APPLIED SCIENCE AND MANUFACTURING · 2020 · IF 6.444

High micromechanical interlocking graphene oxide/carboxymethyl cellulose composite architectures for enhancing the interface adhesion between carbon fiber and epoxy

Baowei Qiu,Tong Sun,Muxuan Li,Yang Chen,Shengtai Zhou,Mei Liang,Huawei Zou

The interface performance of carbon fiber (CF) reinforced polymer composites (CFRPs) is one of the key factors that affect their properties. In order to improve the interface adhesion between CF and epoxy (EP), a green method is proposed. Carboxymethyl cellulose (CMC) and graphene oxide (GO) are introduced to the CF surface through the hydrogen bonds, and they can form high micromechanical interlocking composite architectures, which can enhance the micromechanical interaction in the interface of CF and EP. It is found that CMC and GO can significantly improve the interfacial shear strength (IFSS) and interlaminar shear strength (ILSS) of EP/CF composite. This means that it has great potential to improve the interface of CFRPs and strengthen their performance by natural cellulose fibers. This modification method does no harm to CF and is environmental friendliness, which lays a research foundation for using natural cellulose to enhance the interface performance of CFRPs.

研究领域: 复合材料科学 · 高分子材料 · 界面工程 · 纳米材料 · 绿色制造
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