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DESIGNED MONOMERS AND POLYMERS · 2019 · IF 1.528

Preparation and application of macromolecules with a fluorescence effect in polymer processing

Meng-Di Chen,Guo Zhang,Shi-Chang Chen,Xian-Ming Zhang,Wen-Xing Chen

In this study, 9-anthracenemethyl methacrylate (AMMA) and styrene (St) as monomers and benzoyl peroxide as an initiator were used to synthesize P(St-co-AMMA), a macromolecule tracer with a fluorescence effect, via free radical copolymerization. A fluorescent online detection device was built on the basis of the principle of fluorescence online detection by using the single-screw extrusion platform of a torque rheometer to explore the effect of the amount of macromolecular tracer and screw speed on the residence time distribution of polystyrene in single-screw extrusion. Fourier transform infrared spectroscopy, 1H-NMR, thermal stability, fluorescence properties, and rheological properties show that the resulting product P(St-co-AMMA) has a degree of thermal stability, fluorescence, and rheological properties similar to polystyrene, so this product can be used to characterize the residence time distribution during single-screw extrusion. The amount of macromolecular tracer P(St-co-AMMA) does not affect the residence time distribution of polystyrene during single-screw extrusion processing, meanwhile, the minimum residence time decreases and the residence time distribution becomes narrow as the screw speed increases, that is, the axial mixing capacity of the single-screw extruder decreases as the screw speed increases.

研究领域: 高分子化学 · 材料科学 · 聚合物加工工程
✓ 已验证 产品关联 DOI PubMed 高影响因子
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International Journal of Electrochemical Science · 2023 ·Vol. 13 ·期 12 ·11953-11960 · IF 1.5

Electrochemical Sensor Based on Molecularly Imprinted Polymer for Determination of Nonylphenol

Benzhi Liu,Jinlong Yan,Min Wang,Xiangyang Wu

Molecularly imprinted polymers were prepared on the surface of acrylamide-functionalized multi-walled carbon nanotubes by thermal polymerization, which using nonylphenol as template molecule, methacrylic acid as functional monomer and ethyleneglycol dimethacrylate as crosslinking agent. The molecularly imprinted polymers were modified on the surface of glassy carbon electrode to prepare electrochemical sensor. The proposed sensor showed a linear range of 0.1 to 30 μM with a detection limit of 0.02 μM. The sensor exhibited good stability, selectivity and high sensitivity to nonylphenol detection. It was successfully applied to detect nonylphenol in water samples.

研究领域: 分析化学 · 环境监测 · 材料科学 · 电化学 · 传感器技术
✓ 已验证 DOI 高影响因子
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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
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 25 · IF 1.768

Rapid ambient temperature living radical polymerization of methyl methacrylate and styrene utilizing sodium hypophosphite as reducing agent

Xiao-Hui Liu,Fei-Jun Zhang,Hui-Na Li,Xiao-Hui Hu,Wen-Li Di,Shuang Zhao

A facile, safe, and inexpensive reducing agent, sodium hypophosphite (NaH 2 PO 2 ·H 2 O), has been successfully used to perform ambient temperature living radical polymerizations of methyl methacrylate (MMA) and styrene (St). The rapid radical polymerizations were readily obtained at 25°C, i.e., MMA reached a conversion of ca 90% after 2.5 h, and St reached a conversion of ca 80% after 40 h. The polymerizations of MMA and St exhibited excellent living/controlled nature, as evidenced by pseudo first-order kinetics of polymerization, linear evolution of molecular weights with increasing monomer conversions, and narrow molecular weight distributions. The various experimental parameters—ligand, solvent, and molar ratio of NaH 2 PO 2 ·H 2 O to CuSO 4 ·5H 2 O—were varied to improve the control of polymerization, molecular weight, and molecular weight distribution. 1 H NMR analyses and chain-extension reactions confirm the high chain-end functionality of the resultant poly(methyl methacrylate) and polystyrene. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42123.

研究领域: 高分子化学 · 聚合反应工程 · 功能高分子材料 · 可控/活性聚合 · 绿色合成方法
✓ 已验证 DOI 高影响因子
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POLYMER · 2017 · IF 3.684

Surface and mechanical properties of waterborne polyurethane films reinforced by hydroxyl-terminated poly(fluoroalkyl methacrylates)

Wei Yang,Xu Cheng,Haibo Wang,Yuansen Liu,Zongliang Du

Novel waterborne fluorinated polyurethane (WFPU) based on hydroxyl-terminated poly(fluoroalkyl methacrylates) (HTPFMA) was prepared successfully. The microstructures and micro-phase separation of WFPU were evaluated through infrared spectroscopy (FT-IR), X-ray diffraction (XRD), dynamic mechanical analysis (DMA), and scanning electron microscope (SEM). FT-IR revealed that the H-bonded carbonyl in hard domains increased with the increasing of fluorine content, resulting in enhancing the extent of micro-phase separation between hard and soft segments. XRD results indicated that the crystallinity of hard segment was enhanced with the increasing of fluorine content. The direct visual microstructures by SEM showed that the micro-phase separation was more significant when the fluorine content increased. DMA also revealed strengthened micro-phase separation with increasing fluorine content. The studies of mechanical properties confirmed that WFPU based on HTPFMA had outstanding mechanical properties. The effects of fluorine content on the static contact angles, surface free energy , and surface composition were also studied. The static contact angles of the WFPU films against water and methylene iodide reached around 108° and 84°, respectively. X-ray photoelectron spectroscopy (XPS) confirmed that the fluorine surface enrichment factor in the outermost 10 nm depth was about 10–18 fold higher than its bulk level.

研究领域: 高分子材料科学 · 表面科学 · 材料化学 · 软物质物理 · 功能涂层材料
✓ 已验证 DOI 高影响因子
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Nanoscale · 2015 ·Vol. 8 ·期 5 ·2811-2818 · IF 7.394

Highly sensitive broadband flexible photodetectors based on a blend film with zinc octaethylporphyrin long nanowires embedded in an insulating polymer

Jia-Mei Yang,Feng-Xia Wang,Ge-Bo Pan

Blend films with long nanowires of zinc octaethylporphyrin (ZnOEP) embedded in an insulating polymer of poly(methyl methacrylate) (PMMA) have been successfully fabricated by a one-step spin-coating process. Concerning photoactive blends based on small-molecule semiconductors, this is quite a novel strategy and allows us to greatly reduce the issues related to low device performance, such as phase-separation, poor connectivity of the semiconducting layer, and higher densities of interfacial defects. Intensive studies on the correlation between the film morphology and device performance have revealed that excellent photodetector performance is derived from efficient charge transport and good connectivity observed in highly crystalline, interconnected ZnOEP nanowires embedded in an insulating PMMA matrix. To the best of our knowledge, this is the first demonstration of a blend-film-based organic photodetector, which exhibits high sensitivity, high stability, high Ion/Ioff ratio, excellent mechanical flexibility, and a broadband responsivity region extending up to 1050 nm. The unique characteristics of facile fabrication, high sensitivity, excellent mechanical stability, and broadband responsivity can make the blend film of ZnOEP and PMMA promising in large-area flexible photodetectors.

研究领域: 材料科学 · 纳米科技 · 有机电子学 · 光电子学 · 柔性电子器件
✓ 已验证 DOI 高影响因子
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JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY · 2019 ·Vol. 57 ·期 15 ·1653-1663 · IF 2.591

Schiff base as a novel kind of catalyst for reversible complexation-mediated radical polymerization of methyl methacrylate

Bin Li,Yan Shi,Zhifeng Fu

Two kinds of Schiff base, N , N ′-dibenzylidene-1,2-diaminoethane (NDBE) and N , N ′-disalicylidene-1,2-diaminoethane, have been found as efficient organic catalyst for reversible complexation-mediated radical polymerization (RCMP) of methyl methacrylate (MMA) for the first time. The polymerization results show obvious features of “living”/controlled radical polymerization. Well-defined and low-polydispersity polymers ( M w / M n = 1.20–1.40) are obtained in RCMP of MMA catalyzed by Schiff base at mild temperature (65–80°C). Moreover, Schiff base also exhibits a particularly high reactivity for RCMP of MMA with in situ formed alkyl iodide initiator. The polymer molecular weight and its polydispersity ( M w / M n is around 1.20) are well controlled even with high monomer conversion. Notably, when the dosage of azo initiator is same as the dosage of iodine, the polymerization could also be realized in the presence of NDBE. The living feature of synthesized polymer is confirmed through the chain extension experiment. In short, Schiff base is a kind of high-efficient catalyst for RCMP and reverse RCMP of MMA, which can be one of the most powerful and robust techniques for polymer synthesis. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1653–1663

研究领域: 高分子化学 · 聚合物合成 · 催化化学 · 功能材料 · 有机合成方法学
✓ 已验证 DOI 高影响因子
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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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JOURNAL OF APPLIED POLYMER SCIENCE · 2013 ·Vol. 131 ·期 9 · IF 1.395

Dynamic mechanical properties of semi-interpenetrating polymer network-based on nitrile rubber and poly(methyl methacrylate-co-butyl acrylate)

Chang Su,Dezhen Zong,Lihuan Xu,Cheng Zhang

In this article, semi-interpenetrating polymer network (Semi-IPNs) based on nitrile rubber (NBR) and poly(methyl methacrylate- co -butyl acrylate) (P(MMA-BA)) were synthesized. The structure and damping properties of the prepared Semi-IPNs blends were characterized and by fourier transform infrared spectrum (FTIR), dynamic mechanical analysis (DMA), scanning electron microscopy (SEM), thermogravimetric analysis (TGA/DTG), and tensile mechanical properties. The results showed that interpenetrating network based on P(MMA-BA) and NBR was successfully obtained, which showed the improved thermal stability compared to NBR/P(MMA-BA)-based two-roll mill blends. Furthermore, Semi-IPNs showed significantly better the dynamic mechanical properties than that of the two-roll mill system. With the increasing feed ratio of BA and MMA during the preparation of Semi-IPNs, the loss peak position for P(MMA-BA) in NBR/PMMA IPNs shifted to a lower temperature from 20°C to −17°C, and when NBR in Semi-IPNs was accounted for 40 wt %, the dynamic mechanical thermal analysis showed that much more advanced damping material with wider temperature range (−30°C < T < 80°C) as tan δ > 0.45 can be achieved. Therefore, it was expected as a promising way to obtain the excellent damping materials with good oil-resisted properties according the Semi-IPNs system. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40217.

研究领域: 高分子材料科学 · 功能材料 · 复合材料 · 材料物理 · 阻尼材料 · 聚合物改性
✓ 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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