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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2013 ·Vol. 51 ·期 7 ·1559-1564 · IF 3.543

In situ Cu(0)-mediated single electron transfer living radical polymerization of methyl methacrylate using nickel powder

Xiao-Hui Liu,Yun-Hai Yu,Di Jia,Bo-Wen Cheng,Fei-Jun Zhang,Hui-Na Li,Peng Chen,Shan Xie

Single electron transfer living radical polymerization of methyl methacrylate catalyzed by the in situ prepared Cu(0) at ambient temperature was first examined using various metallic powders, including Zn(0), Ni(0), Mg(0), and Fe(0). Importantly, the polymerization initiated with Ni(0)/EBiB/CuBr 2 /PMDETA system exhibited optimal living/controlled nature and generated polymers with polydispersity index as low as 1.04 for 75.27% conversion and controlled molecular weights close to theoretical ones. A wide of range of Cu(II) salts were also investigated as catalyst sources instead of CuBr 2 . The recycling of Ni(0) was very convenient due to its magnetic property, which enables its extensive application. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013

研究领域: 高分子化学 · 材料科学 · 催化化学 · 有机合成 · 功能材料
✓ 已验证 DOI 高影响因子
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International Journal of Electrochemical Science · 2023 ·Vol. 12 ·期 6 ·5421-5430 · IF 1.5

Membrane Separators Coated by TiO2-PMMA with Low Thermal Shrinkage Rate for Lithium-Ion Batteries

Yangyang Xi,Peng Zhang,Haining Zhang,Zhaohui Wan,Wenmao Tu,Haolin Tang

Composite membrane separators are fabricated by coating one side of microporous polyethylene membrane with poly(methyl methacrylate) modified titanate nanoparticles that are synthesized through emulsifier-free emulsion polymerization of methacrylate-functionalized titanate nanoparticles. The formed composite membrane separators exhibit great thermal-shrinking resistance due to the introduction of thermal resistant titanate nanoparticles. After immersed into electrolyte solution, the swelling poly(methyl methacrylate) microspheres leads to the formation of gel electrolyte, thus stabilizing the electrolyte. Moreover, the porous structure of the coated layer can facilitate the swelling of electrolyte and the transport of lithium ions. The thus-assembled lithium ion battery shows an improved cycle performance and rate capability.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子纳米复合材料 · 电池技术
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2018 · IF 3.909

Dual-responsive IPN hydrogel based on sugarcane bagasse cellulose as drug carrier

Yuanfeng Pan,Jingchun Wang,Pingxiong Cai,Huining Xiao

In this work, the stepwise synthesis of interpenetrating polymer network (IPN) strategy was developed in an attempt to fabricate novel hydrogels consisting of sugarcane bagasse cellulose (SBC), carboxymethylcellulose (CMC) and poly (N-isopropylacrylamide) (PNIPAm) as a dual-responsive drug carrier. The pretreated and dissolved SBC was pre-crosslinked using epichlorohydrin in the presence of CMC, followed by in-situ free-radical polymerization of NIPAm in the presence of N,N′-Methylene-bis(acrylamide) as a crosslinking agent. The carboxyl groups in CMC and PNIPAm chains rendered the resulting hydrogel pH and thermal responsive. The results from scanning electron microscopy, infrared spectroscopy , thermogravimetric analysis and mechanical property testing demonstrated the successful formation of the IPN with proper structure and mechanical strength . The swelling experiments at different temperatures and pH showed the dual–sensibility of the hydrogels. Moreover, bovine serum albumin (BSA) was used as a model drug and loaded in the hydrogel; and the drug release behavior was revealed in phosphate buffer solution (PBS) and simulated gastric fluid (SGF). The results indicated that the dual-responsive IPN hydrogel is of great potential for the controlled release of drug.

研究领域: 高分子材料 · 药物递送 · 生物医学工程 · 智能响应材料 · 药剂学
✓ 已验证 DOI 高影响因子
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JOURNAL OF THE CHINESE CHEMICAL SOCIETY · 2017 ·Vol. 64 ·期 2 ·231-238 · IF 0.935

Effect of Sodium Alginate on the Properties of Thermosensitive Hydrogels

Jie Wu,Zongmei Wu,Xuejiao Sun,Shichao Yuan,Ruling Zhang,Qingliang Lu,Yueqin Yu

Sodium alginate (SA) was combined with poly( N -isopropylacrylamide) (PNIPAAm) to prepare thermosensitive hydrogels through semi-interpenetrating polymer network (semi-IPN) and fully interpenetrating polymer network (full-IPN). The thermosensitive, swelling, mechanical, and thermal properties of pure PNIPAAm, SA/PNIPAAm semi-IPN, and Ca-alginate/PNIPAAm full-IPN hydrogels were investigated. The formation of semi-IPN and full-IPN significantly improved the hydrogels’ swelling capability and mechanical properties without altering their thermosensitivity. 5-Fluorouracil (5-Fu) was selected as a model drug to study the release behaviors of the hydrogels. It was found that in vitro controlled drug release from semi-IPN hydrogels showed an initial release burst, followed by a slower and sustained release, before reaching equilibrium. Full-IPN hydrogels showed slow and sustained release during the whole process. Temperature and pH were found to affect the rate of drug release. Ca-alginate/PNIPAAm full-IPN hydrogels have potential application as drug delivery matrices in controlled drug release.

研究领域: 生物材料 · 药剂学 · 高分子科学 · 组织工程 · 药物递送系统
✓ 已验证 DOI 高影响因子
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INTERNATIONAL JOURNAL OF PHARMACEUTICS · 2013 · IF 3.458

A novel pulsatile drug delivery system based on the physiochemical reaction between acrylic copolymer and organic acid: In vitro and in vivo evaluation

Ziwei Zhang,Xiaole Qi,Xiangbo Li,Jiayu Xing,Xuehua Zhu,Zhenghong Wu

Multilayer-coating technology is the traditional method to achieve pulsatile drug release with the drawbacks of time consuming, more materials demanding and lack of efficiency. The purpose of this study was to design a novel pulsatile drug delivery system based on the physiochemical interaction between acrylic copolymer and organic acid with relatively simpler formulation and manufacturing process. The Enalapril Maleate (EM) pulsatile release pellets were prepared using extruding granulation, spheronization and fluid-bed coating technology. The ion-exchange experiment, hydration study and determination of glass transition temperature were conducted to explore the related drug release mechanism. Bioavailability experiment was carried out by administering the pulsatile release pellets to rats compared with marketed rapid release tablets Yisu ® . An obvious 4   h lag time period and rapid drug release was observed from in vitro dissolution profiles. The release mechanism was a combination of both disassociated and undisassociated forms of succinic acid physiochemically interacting with Eudragit ® RS. The AUC0-τ of the EM pulsatile pellets and the market tablets was 702.384   ±   96.891   h   ng/mL and 810.817   ±   67.712   h   ng/mL, while the relative bioavailability was 86.62%. These studies demonstrate this novel pulsatile release concept may be a promising strategy for oral pulsatile delivery system.

研究领域: 药剂学 · 药物递送 · 生物药剂学 · 药物代谢 · 制剂工程 · 药动学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2012 ·Vol. 125 ·期 4 ·2867-2873 · IF 1.289

Synthesis of fluorescent poly(1-vinylimidazole-co-(1-pyrene) methyl 2-methyl-2-propenote) and determination of monomer reactivity ratios

Yehai Yan,Na Lu,Jian Cui,Jinfang Zhang

A new fluorescent copolymer, poly(1-vinylimidazole- co -(1-pyrene) methyl 2-methyl-2-propenote) (VI- co -PyMMP), has been designed and synthesized by a free-radical copolymerization of VI and PyMMP as well as characterized using ultraviolet (UV), Fourier transform infrared spectroscopy (FTIR), 1 H NMR, and fluorescence spectroscopies. The monomer reactivity ratios are determined by two methods of Fineman-Ross ( r 1 = 0.28 ± 0.04 for VI, r 2 = 1.32 ± 0.11 for PyMMP) and Kelen-Tüdös ( r 1 = 0.23 ± 0.05, r 2 = 1.22 ± 0.12). Based on the reactivity ratios, the monomer sequence lengths and Q and e for PyMMP monomer are further calculated. The results suggest that the copolymerization of VI and PyMMP is a nonideal copolymerization without an azeotropic point (i.e., r 1 < 1, r 2 > 1 and r 1 r 2 < 1) and has a low alternation tendency. The conclusions drawn in this work may not only direct the later synthesis of the copolymers but also enrich the database of free-radical copolymerization. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012

研究领域: 高分子化学 · 功能高分子 · 荧光材料 · 聚合物合成 · 材料化学
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2018 · IF 4.439

Phase inversion, formation and stability mechanism of poly(urethane-acrylate) nanoemulsions based on block-copolymer surfmer

Haihua Wang,Bei Li,Guiqiang Fei,Yiding Shen,Ke Zhu

We reported herein the synthesis of block copolymers and their application in the in-situ emulsion polymerization of waterborne poly (urethane-acrylate) (WPUA) nanoemulsions based on phase inversion process. The polymerizable surfmers containing terminal unsaturated double bonds (MSA-r) were successfully synthesized via catalytic chain transfer polymerization (CCTP). Random copolymer (MSA-t) prepared through radical polymerization was utilized as control. The structure, surface tension and aggregation behavior of surfmers were characterized. The phase inversion, formation and stability of WPUA nanoemulsions were systematically investigated. Effects of MSA-r surfmer content and BMA/MMA ratio on the water resistance and thermal stability of the corresponding films were also discussed. It was found that the phase inversion mechanism of PUA prepolymer in the presence of MSA-r surfmers is different from conventional polyurethane prepolymer. The addition of MSA-r and MSA-t surfmers alters the rheological behaviors of PUA prepolymer via PUA-surfmer interactions, as well as the phase inversion process. Compared with WPUA/MSA-t emulsion, WPUA/MSA-r nanoemulsion displayed improved stability at higher solid content. The minimum particle size of WPUA/MSA-r nanoemulsion was 88.7 nm and kept almost constant after 12-month storage, while the particle size of WPUA/MSA-t emulsion was 131.3 nm and increased to 178.9 nm. Moreover, the WPUA/MSA-r film possessed improved water resistance and thermal stability.

研究领域: 高分子化学 · 胶体与界面科学 · 材料化学 · 纳米材料 · 功能高分子 · 水性涂料 · 聚合物乳液
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 133 ·期 1 · IF 1.768

Surface-modified MgO nanoparticle enhances the mechanical and direct-current electrical characteristics of polypropylene/polyolefin elastomer nanodielectrics

Yao Zhou,Jinliang He,Jun Hu,Bin Dang

Polypropylene (PP)/polyolefin elastomer (POE) blends and MgO/PP/POE nanocomposites were fabricated by melt blending. The morphology, mechanical, and electrical properties of the nanocomposites were investigated. Scanning electron microscopy showed that the surface-modified MgO nanoparticles were well dispersed in the polymer matrix at low loadings of less than 3 phr. X-ray diffraction demonstrated that the crystalline phases of PP in the composites were changed and that the β phase significantly increased. An examination of the electrical properties revealed that the direct-current (dc) electric breakdown strength and space-charge suppression effect were remarkably improved by the introduction of the surface-modified MgO nanoparticles. In addition, obvious enhancements in the tensile modulus and strength were obtained as a result of the synergistic toughening of the POE and MgO nanoparticles. Thus, MgO/PP/POE nanocomposites with enhanced mechanical and electrical properties have great potential to be used as recyclable insulation materials for high-voltage dc cables with large transmission capacities and high operating temperatures. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 132 , 42863.

研究领域: 高分子材料科学 · 电气工程材料 · 纳米复合材料 · 介电物理 · 绝缘材料
✓ 已验证 DOI 高影响因子
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Advances in Materials Science and Engineering · 2018 ·Vol. 2018 ·期 1 ·7252809 · IF 1.372

Enhanced Red Emission in Ultrasound-Assisted Sol-Gel Derived ZnO/PMMA Nanocomposite

Van-Tuan Mai,Quang-Bac Hoang,Xuan-Dung Mai

Cost-effective methods for preparing ZnO nanostructures are of importance for the deployment of ZnO in many applications including n-type conduits, catalysts, nanophosphor, and optoelectronics. Herein, we present a room-temperature sol-gel method with the aid of ultrasonication to prepare white-emitting ZnO nanoparticles (NPs). X-ray diffraction and electron microscopic analyses revealed that the size and shape of ZnO NPs can be controlled simply by changing the concentration of the Zn precursor. The ZnO NPs had a broad photoluminescence emission, ranging from 450 nm to 800 nm, while their composite in PMMA matrix showed an enhancement in the red region induced by ZnO-PMMA interfacial band-bending effects. The results demonstrated herein promise a simple tool for control over size, shape, and emission of ZnO materials for diverse applications.

研究领域: 材料科学 · 纳米技术 · 光电子学 · 高分子化学 · 发光材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 46 ·45484 · IF 1.86

Copper(I) bromide coordinated by the ionic liquid 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride to catalyze the atom transfer radical polymerization of methyl methacrylate in 1-allyl-3-methyl imidazolium chloride

Teng Xue,Erjun Tang,Jian Zhou,Ruitao Han,Shaojie Liu

A coordinating ionic liquid (IL), 1-[(diethyl amine)amine]ethyl-3-methyl imidazolium chloride ([N 3 MIM]Cl), was prepared as an alternative to a simple organic ligand to coordinate to copper(I) bromide (CuBr). We, thereby, obtained a novel catalyst for atom transfer radical polymerization (ATRP) reactions. This catalyst was applied to the ATRP of methyl methacrylate in the IL 1-allyl-3-methyl imidazolium chloride ([AMIM]Cl). The chemical structures of the ILs obtained were confirmed by Fourier transform infrared spectroscopy, mass spectrometry, and 1 H-NMR analyses. The coordination ability of [N 3 MIM]Cl was assessed by cyclic voltammetry, and the redox potential of [N 3 MIM]Cl–CuBr was −0.507 V. The [N 3 MIM]Cl–CuBr complex was expected to be a markedly more active catalyst than the amine DETA–CuBr complex. The coordination mode toward CuBr was also examined. The [N 3 MIM]Cl–CuBr catalyst system showed good controllability in the aforementioned ATRP reaction in [AMIM]Cl. The Cu catalyst was easily separated from the obtained polymer with the coordinating IL as a ligand. Consequently, the coordinating IL overcame the shortcomings of traditional organic ligands, such as poor compatibility with IL media and poor separation of the catalyst from the polymer; this makes it highly promising for applications in the ATRP field. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45484.

研究领域: 高分子化学 · 催化化学 · 功能材料 · 绿色溶剂 · 配位化学 · 电化学
✓ 已验证 DOI 高影响因子
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Small · 2024 ·Vol. 21 ·期 5 ·2408929 · IF 13

High Tribo-Charge Density Composite Nanofiber Membrane for Motion Sensing and Water Wave Energy Harvesting

Xue Jiao Zhao,Zhi Hao Zhao,Zhong Lin Wang,Guang Zhu,Jie Wang

Triboelectric nanogenerators (TENGs), among the most simple and efficient means to harvest mechanical energy, have great potential in renewable energy utilization. While the output performance of TENGs is still not high enough, which limits its practical application. Here, a poly(vinylidene fluoride) (PVDF)/fluorinated ethylene propylene nanoparticles (FEP NPs) porous nanofiber (PFPN) membrane with waterproof, breathable, surface superhydrophobic and high tribo-negative properties is proposed for achieving high-performance of TENGs. The PFPN-based solid–solid contact PFPN-TENG achieved an optimal electric output with a net tribo-charge density of 294 µC m −2 , which is 42.2% more than that of polytetrafluoroethylene (PTFE) film. The PFNP membrane can maintain the best performance with almost no attenuation after 142680 working cycles. Based on its excellent triboelectric characteristics, the PFPN membrane shows its excellent performance for self-powered body motion sensing and mechanical energy harvesting. A flexible solid–liquid contact PFPN-TENG can achieve high electrical output with an average volume power density of ≈544.1 W m −3 by harvesting water wave energy. Such excellent performance of the PFPN membrane makes it a potential candidate to promote the power density of TENGs in harvesting blue water wave energy.

研究领域: 纳米能源材料 · 柔性电子学 · 生物医学工程 · 可穿戴设备 · 环境能量收集
✓ 已验证 DOI 高影响因子
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2019 ·Vol. 220 ·期 18 ·1900299 · IF 2.622

Solventless Synthesis and Patterning of UV-Responsive Poly(allyl methacrylate) Film

Huidong Yang,Hong Wang,Jingang Feng,Yumin Ye,Wenna Liu

Asymmetric divinyl monomers are attractive candidates for constructing functional polymer thin films owing to their ability to undergo further reactions after polymerization. Here, the first solventless synthesis of poly(allyl methacrylate) (PAMA) film with retention of abundant allyl groups using initiated chemical vapor deposition (iCVD) is reported. It is demonstrated that lower substrate and filament temperatures lead to better allyl retention, while higher temperatures lead to intramolecular cyclization. The retained allyl groups can be further crosslinked under UV light, and the crosslinking degree can be easily tuned by adjusting the exposure time. Patterning of iCVD PAMA films with 20 µm resolution using a TEM grid as photomask is also demonstrated. The reported synthesis method suggests possible solventless incorporation of AMA in thin films as a latent crosslinker or anchoring sites for further functionalization. The solventless patterning can also extend patterning technique to solvent-sensitive and non-planar substrates.

研究领域: 高分子材料科学 · 表面化学 · 功能薄膜 · 光响应材料 · 生物医学工程
✓ 已验证 DOI 高影响因子
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