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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 15 · IF 1.64

Preparation and application of sulfadiazine surface molecularly imprinted polymers with temperature-responsive properties

Pengfei Ma,Zhiping Zhou,Wenming Yang,Bingqing Tang,Hong Liu,Wanzhen Xu,Weihong Huang

Novel, temperature-responsive molecularly imprinted polymers (TMIPs) based on potassium hexatitanate whiskers for selectively adsorbing sulfadiazine (SDZ) from aqueous media were prepared with methacrylic acid (MAA) and 4-vinylpyridine (4-VP) as cofunctional monomers and N -isopropyl acrylamide (NIPAM) as a temperature-responsive monomer. The template–monomer interactions were studied by molecular simulation. In particular, the effects of different kinds of crosslinkers on the selective recognition ability of the TMIPs in water media were investigated. The temperature–responsive adsorption performance and phase behavior of the molecularly imprinted polymers were studied by batch-mode binding experiments, swelling experiments, and contact angle testing. The results demonstrate that the combination of MAA, 4-VP, and NIPAM was a favorable temperature-responsive imprinted system for SDZ in water, and the cocrosslinking agent of ethylene glycol dimethacrylate (EGDMA) and N,N ′-methylene bisacrylamide (MBA) was more suitable compared with either pure EGDMA or MBA. The adsorption kinetics and adsorption isotherms were analyzed by the fitting of different adsorption models. Also, the effect of the temperature on the recovery was investigated by the determination of the spiked SDZ in real-water samples with solid-phase extraction and high-performance liquid chromatography. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41769.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 15 · IF 1.64

Optimal design of an imprinted preassembled system by quantum chemical calculations and preparation of a surface-imprinted material for the selective removal of quinoline

Wenming Yang,Pengfei Ma,Ting Fan,Zhiping Zhou,Hong Liu,Wanzhen Xu

In this study, we examined the rational preparation of molecularly imprinted polymers (MIPs) for the selective removal of quinoline from octane. Before the preparation, density functional theory, as one of the methods of quantum chemical calculation, was used for the simulation of a quinoline-imprinted preassembly system. Methacrylic acid turned out to be the more suitable monomer for quinoline compared with acrylamide, and different template–monomer ratios, including 1:1, 1:2, and 1:3, were studied and are discussed. On the basis of the result of molecular simulation, quinoline-imprinted polymers were prepared with a combination of surface imprinting and living polymerization. The prepared quinoline–MIPs were characterized and used as selective adsorbents for batch-mode binding experiments. The fitting result of the adsorption data indicates that the adsorption kinetics and adsorption isotherms of the quinoline-imprinted polymers fit well a pseudo-second-order kinetics model and the Freundlich model, respectively. A selective recognition ability was demonstrated by equilibrium binding analysis. This study will provide needful guidance and a theoretical basis for the preparation of imprinted materials in the field of industrial denitrification. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41730.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 15 · IF 1.64

Preparation and characterization of printable solder resist inks based on hyperbranched polyester

Chao Yang,Yu Chang,Zhen-Guo Yang

Two novel solder resist inks containing hyperbranched epoxy resin (HBPE) for thermal curing and hyperbranched epoxy acrylate resin (HBPEA) for UV-curing were introduced in this work. Different generations of HBPE and HBPEA were synthesized and their chemical structures were determined by FT-IR. Both curing reactions were monitored under differential scanning calorimetry (DSC) and photo-DSC. For HBPE, the curing temperature of 7th generation was only 91°C and for HBPEA, the curing duration of 7th generation was under 10 s. The thermal stabilities of cured resins were much more stable than linear resin, as the decomposition temperatures of HBPE and HBPEA were both over 400°C. The ink containing HBPE or HBPEA jetted by piezoelectric printer showed excellent accuracy and consistency of linewidth and the morphologies of cured pattern were observed through a stereo microscope. Other performances of solder masks were tested under China Printed Circuit Association (CPCA) standard (CPCA/JPCA 4306-2011), which satisfy all requirements of printed circuit board soldering procedure. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41805.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 20 · IF 1.64

Synthesis, characterization, and properties of a polyhedral oligomeric octadiphenylsulfonylsilsesquioxane

Ziqian Li,Rongjie Yang

A novel polyhedral oligomeric octadiphenylsulfonylsilsesquioxane (ODPSS) was synthesized from octaphenylsilsesquioxane and benzenesulfonyl chloride via a Friedel–Crafts reaction with a high yield. ODPSS was identified by Fourier transform infrared spectroscopy, 1 H-NMR, 13 C-NMR, 29 Si-NMR, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI–TOF MS), wide-angle X-ray diffraction, and elemental analysis to be a kind of polyhedral oligomeric silsesquioxane of a T 8 R 8 structure. ODPSS exhibited superior thermal stability according to thermogravimetric analysis. Its initial thermal decomposition temperature ( T onset ) was at 491°C in air and 515°C in nitrogen. Thermal and mechanical properties of epoxy resin (EP) composites with ODPSS added were studied by differential scanning calorimetry and tensile testing. The results show that the incorporation of ODPSS at a low loading content not only improved the glass-transition temperature of the EP composites but also enhanced their tensile strength. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40892.

CAS / MDL: 98-09-9
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 20 · IF 1.64

Preparation of polymer electrolytes based on the polymerized imidazolium ionic liquid and their applications in lithium batteries

Mingtao Li,Lu Wang,Tingting Du

The polymer electrolytes based on a polymerized ionic liquid (PIL) as polymer host and containing 1,2-dimethyl-3-butylimidazolium bis(trifluoromethanesulfonyl)imide (BMMIM-TFSI) ionic liquid, lithium TFSI salt, and nanosilica are prepared. The PIL electrolyte presents a high ionic conductivity, and it is 1.07 × 10 −3 S cm −1 at 60°C, when the BMMIM-TFSI content reaches 60% (the weight ratio of BMMIM-TFSI/PIL). Furthermore, the electrolyte exhibits wide electrochemical stability window and good lithium stripping/plating performance. Preliminary battery tests show that Li/LiFePO 4 cells with the PIL electrolytes are capable to deliver above 146 mAh g −1 at 60°C with very good capacity retention. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40928.

CAS / MDL: 112945-52-5
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 10 · IF 1.64

The chlorination and chlorine resistance modification of composite polyamide membrane

Hao Li,Ping Yu,Haigang Li,Yunbai Luo

Membrane-based separation technology is one of the most active separation technologies being employed in water treatment. Polyamides (PA) are widely used membrane materials because they exhibit excellent performance, such as high flux with high salt rejection, and enhanced stability against wide range of pH and temperature. Unfortunately, PA membranes exhibit extremely poor resistance to chlorine leading to increased operation costs and decreased membrane lifetime. In this study, we find new ways for prolonging membrane lifetime and reducing the operating costs by investigating the chlorination and modification of PA membranes. Varying concentrations of hypochlorite were used to chlorinate a commercial reverse osmosis membrane (BW-30, DOW). The results showed that short-time exposure to high concentrations of hypochlorite could cause more serious problems to membranes than long-time exposure to low concentrations under the similar total exposure. The performance of the chlorinated membranes was recovered to some extent after treatment with NaOH solution (pH 10), indicating that the alkali treatment could initiate the reversible regeneration of chlorinated membranes. Furthermore, an industrial grade epoxy resin was used to modify the membranes to enhance the chlorine resistance via the reaction between the amide nitrogen and epoxy bond. The successful modifications were confirmed by attenuated total reflectance Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, and atomic force microscopy. Moreover, the chlorination tests showed that the modifications performed in these experiments enhanced the chlorine resistance of the membranes, especially for the membranes exposed to low concentration of chlorine. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41584.

CAS / MDL: 7681-52-9
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 12 · IF 1.64

Synthesis of phosphorus-containing flame-retardant antistatic copolymers and their applications in polypropylene

Qi Li,Yiquan Chen,Xinpu Song,Yingpeng Xie,Qiong Hou,Guang Shi

By adjusting the molar ratios of antistatic monomer of octyl phenol ethylene oxide acrylate (denoted as AS), rigid monomer of methyl methacrylate (denoted as MMA), and flame-retardant monomer of 2-(phosphoryloxymethyl oxyethylene) acrylate (denoted as FR), a series of flame-retardant antistatic copolymers poly (octyl phenol ethylene oxide acrylate-co-methyl methacrylate-co-phosphoryloxymethyl oxyethylene acrylate) (donated as AMF) were synthesized through radical polymerization. Among the obtained copolymers, two copolymers, AMF162 (the feed molar ratio of AS, MMA, and FR as 1 : 6 : 2) and AMF1104 (the feed molar ratio of AS, MMA, and FR as 1 : 10 : 4) with different concentrations were added into polypropylene (PP) to prepare PP-AMF162 and PP-AMF1104 series of composites. The thermal stability, limiting oxygen index, the antistatic property, and mechanical properties of PP composites were tested and analyzed. PP-AMF162 series composites have excellent antistatic effect. When the AMF162 content was equal to or <15 wt %, the impact strength of PP-AMF162 composites was higher than that of pure PP. The results indicated that copolymer AMF162 was a suitable flame-retardant and antistatic additive for PP. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41677.

CAS / MDL: 7758-89-6 818-61-1
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 11 · IF 1.64

Taurine as an additive for improving the fouling resistance of nanofiltration composite membranes

Jinbo Jin,Dongqing Liu,Dandan Zhang,Yuhang Yin,Xinyu Zhao,Yufeng Zhang

A hydrophilic compound, taurine, was investigated as an additive in the interfacial polymerization between piperazine (PIP) and trimesoyl chloride (TMC) to prepare thin-film composite (TFC) membranes. The resulting membranes were characterized by X-ray photoelectron spectroscopy and attenuated total reflectance–Fourier transform infrared spectroscopy. The morphology and hydrophilicity of the membranes were investigated through scanning electronic microscopy and water contact angle measurements. The separation performance of the TFC membranes was investigated through water flux and salt rejection tests. The protein-fouling resistance of the films was evaluated by water recovery rate measurements after the treatment of bovine serum albumin. The membrane containing 0.2 wt % taurine showed the best performance of 92% MgSO 4 rejection at a flux of 31 L m −2 h −1 and better antifouling properties than the PIP–TMC membranes. An appropriately low concentration of taurine showed the same MgSO 4 rejection as the PIP–TMC membranes but a better fouling resistance performance. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41620.

CAS / MDL: 9048-46-8
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 11 · IF 1.64

Electrospun dendritic ZnO nanofibers and its photocatalysis application

Jianing Li,Zhiqiang Cheng,Mengzhu Liu,Mingyue Zhang,Meijuan Hu,Li Zhang,Haifeng Jiang,Junfeng Li

A simple and efficient procedure has been developed to fabricate ZnO nanofibers with dendritic structure via electrospinning and subsequent calcination. The spinning solution is prepared by mixing polyvinylpyrrolidone (PVP) and zinc acetate into methanol. From SEM images, it can be observed that the ZnO product has a tendency of dendritic structure. The diameter of the dendritic branch is ∼137 nm. The structure and physicochemical property of the prepared nanofibers are elucidated by TGA, SEM, XRD, FTIR, and PL, respectively. The photoluminescene measurement of the ZnO samples exhibit a broad visible emission band concentrate on around 430–580 nm. Meanwhile, the intensity is related to the content of surface oxygen vacancies, which probably influence photocatalytic activity of ZnO samples. Whereafter, the photocatalytical activity of the ZnO nanofibers is evaluated by quantifying the degradation of methyl blue. The result indicates that ZnO nanofibers annealed at 650°C show an excellent photocatalytic activity. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41627.

CAS / MDL: 25249-54-1 9003-39-8
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 9 · IF 1.64

Effect of a chain extender on the properties of poly(lactic acid)/zinc oxide/copper chlorophyll acid antibacterial nanocomposites

Weihua Fan,Yue Zhao,Aijing Zhang,Yukun Liu,Yanxia Cao,Jinzhou Chen

Poly(lactic acid) (PLA)/nano zinc oxide/copper chlorophyll acid (CCA) antibacterial nanocomposites with excellent mechanical properties were prepared in the presence of a chain extender named tolylene diisocyanate (TDI). The effect of the chain extender on the PLA long chain was confirmed by the increased molecular weight shown in the mass flow rate and gel permeation chromatography. Escherichia coli were adopted to examine the antibacterial ability of the blends. The effect of CCA is also discussed with regard to the enhancement of the antibacterial effect of zinc oxide (ZnO) over E. coli . Scanning electron microscopy and transmission electron microscopy were used to view the agglomeration and dispersion of ZnO in the PLA matrix. Differential scanning calorimetry and thermogravimetric analysis revealed a relatively stable thermal performance of the nanocomposites with and without TDI. A sharp increase in the mechanical properties was also observed after the addition of the chain extender under different processing conditions. Additionally, we found that the nanocomposites with the incorporation of TDI and the masterbatches in batches effectively improved the mechanical properties of PLA/ZnO/CCA without a sacrifice of the antibacterial effect. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41561.

CAS / MDL: 1314-13-2
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 9 · IF 1.64

pH-sensitive keratin-based polymer hydrogel and its controllable drug-release behavior

Juhua Guo,Sujuan Pan,Xiaochun Yin,Yu-Feng He,Tao Li,Rong-Min Wang

Using feather keratin as biocompatible and inexpensive natural biopolymer and methacrylic acid as a functional monomer, we prepared a pH-sensitive feather-keratin-based polymer hydrogel (FKPGel) with grafted copolymerization. The obtained FKPGel was characterized by Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. The swelling behavior and pH sensitivity of the FKPGel were investigated. When the small molecule (rhodamine B) and macromolecule (bovine serum albumin) were used as model drug molecules, the FKPGel exhibited controllable release behavior in vitro, and the hydrogels had pH sensitivity. For a small molecular drug, the cumulative release rate was 97% in 24 h at pH 8.4. For macromolecular drug, the cumulative release rate reached 89% at pH 7.4. Its release behavior could be controlled by the pH value. In summary, a simple method was found to reuse disused feathers. It is a kind of pH-sensitive hydrogels to be applied in drug-delivery systems. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41572.

CAS / MDL: 9048-46-8
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 132 ·期 9 · IF 1.64

Polystyrene/attapulgite nanocomposites prepared via in situ suspension polymerization with redox initiation system

Haicun Yang,Liu Zhang,Wenzhong Ma,Hongting Pu,Fanghong Gong

A series of polymer–clay nanocomposites consisting of polystyrene (PS) and attapuglite (ATP) were prepared successfully. First, silane coupling agent containing aromatic tertiary amine groups was synthesized to functionalize ATP (M-ATP). Then, PS nanocomposites with varied clay loadings were prepared via in situ suspension polymerization process with a redox initiation system consisting of aromatic tertiary amine and benzoyl peroxide. The synthesis of silane coupling agent and functionalization of ATP were confirmed by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance spectra, and X-ray photoelectron spectroscopy. Mechanical properties, morphology, thermal stability, and rheological behavior of nanocomposites were investigated to illuminate the effects of M-ATP on the structure and properties of nanocomposites. Field-emission scanning electron microscope images revealed an ideal dispersion of M-ATP and an enhanced toughness of nanocomposites. The improved interface interaction between M-ATP and PS matrix endowed the nanocomposites with outstanding mechanical properties and thermal stability. The formation of hybrid network in the nanocomposites containing 3 wt % M-ATP resulted in higher complex viscosity (η*), storage modulus ( G ′), and lower loss factor (tanδ) compared with the pristine PS and PS/ATP nanocomposites. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41567.

CAS / MDL: 919-30-2 80-41-1
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