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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 19 · IF 1.64

Effect of cross-linked polycarboxylate-type superplasticizers on the properties in cementitious system

Hailu Liu,Hao Pang,Juhua Ou,Lei Zhang,Yongqiang Dai,Bing Liao

Fluidity and slump loss are main technical indicators for the quality of concrete. They are related to the dispersion of cement and hydration process, and are greatly affected by the structure of superplasticizers (SPs). For the purpose of obtaining SPs with excellent fluidity and slump retention, water-soluble cross-linked polycarboxylate ether copolymers (CLPCs) of acrylic acid and alkenyl alcohol type polyoxyethylene ether were synthesized. In order to gain full understanding of the effect of cross-linked SPs on the properties in cementitious system, properties of the new SPs in cement paste were compared to those of traditional ones without cross-linking agents. Mortar tests showed that CLPC performed obvious slow-release function and kept about 10 mm higher than its initial paste flow after 150 min, while PC incurred loss of 15 mm after 150 min. Adsorption of CLPC on cement resulted in zeta potential being roughly the same as that in the case of PC, and enabled more effective slump retention to cement suspensions by rheological property tests. Ettringite peaks disappeared for CLPC on 1-day curve and reappeared after 35 days, and the intensity of CH peaks for CLPC appeared weaker than Blank and PC after 1 day. The microstructure of CLPC after 1 day showed a very dense structure of smaller and thinner crystallites, which indicated that the early hydration was greatly delayed. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40856.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 18 · IF 1.64

Synthesis, characterization, and properties of biodegradable poly(butylene succinate) modified with imide dihydric alcohol

Wen He,Jianwu Lan,Xia Huang,Jiaojiao Shang

A series of high molecular weight poly (butylene succinate) and its copolyester containing rigid imide units were synthesized in this article. The chemical structure and composition of the copolyesters were determined by 1 H NMR spectroscopy and Fourier transform infrared spectroscope (FT-IR). The thermal properties, crystallization behavior and mechanical properties of polymers were investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), wide-angle X-ray diffraction (WAXD) and mechanical testing. The enzymatic degradation was investigated using pancreatic lipase solution. The results showed that the melting temperature ( T m ) of the copolyester decreased with the increment in pyromellitic imide unit content. However, the thermal degradation temperature (5% decomposition temperature) changed little. Meanwhile, the enzymatic degradation rate of poly (butylene succinate) was enhanced. The mechanical properties showed that the tensile strength had a trend of decrease, but the elongation at break was improved with the increment in imide units. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40807.

CAS / MDL: 9001-62-1 89-32-7
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 18 · IF 1.64

Adsorption of Hg(II) in aqueous solutions using mercapto-functionalized alkali lignin

Yan Zhou,Jianping Zhang,Xuegang Luo,Xiaoyan Lin

A novel adsorbent for Hg(II), mercapto-functionalized alkali lignin (AL-SH) was synthesized by Friedel–Crafts alkylation reaction and nucleophilic substitution reactions. The adsorbent was characterized by the techniques of Fourier transform-infrared spectroscopy (FT-IR), elementary analysis and thermogravimetric analysis, and N 2 adsorption techniques. The effect of various parameters on Hg(II) adsorption process such as initial pH, contact time, ionic strength, initial Hg(II) concentration, temperature, and adsorbent dosage were investigated in detail through batch static experiments. The results indicated that the adsorption process of Hg(II) on AL-SH was mainly dependent on the pH and the optimal pH value was at pH ranging from 4.0 to 6.0. The adsorption process was found to follow pseudosecond-order kinetics and the main process was chemical adsorption, which equilibrated at 8 h. The adsorption isotherm was better described by Langmuir and Temkin isotherm equations compared to Freundlich isotherm equation and the maximum adsorption capacity obtained was 101.2 mg g −1 (pH = 4.0, 20°C, initial Hg(II) concentration was 200 mg L −1 ). The thermodynamic parameters of and were positive while was negative, revealed that the adsorption of Hg(II) onto AL-SH was a spontaneous and endothermic process with increased entropy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40749.

CAS / MDL: 14337-53-2
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

Preparation and application in drug controlled delivery of pH-sensitive P(CE-co-DMAEMA-co-MEG) hydrogel

Fang Ping Wang,Jun Ying Zhang,Hu Po Mu,Wan Xia Li,Ting Yuan,Xin Zhen Du

A pH-sensitive hydrogel [P(CE- co -DMAEMA- co -MEG)] was synthesized by the free-radical crosslinking polymerization of N,N -dimethylaminoethyl methacrylate (DMAEMA), poly(ethylene glycol) methyl ether methacrylate(MPEG-Mac) and methoxyl poly(ethylene glycol)-poly(caprolactone)-methacryloyl methchloride (PCE-Mac). The effects of pH and monomer content on swelling property, swelling and deswelling kinetics of the hydrogels were examined and hydrogel microstructures were investigated by SEM. Sodium salicylate was chosen as a model drug and the controlled-release properties of hydrogels were pilot studied. The results indicated that the swelling ratios of the gels in stimulated gastric fluids (SGF, pH = 1.4) were higher than those in stimulated intestinal fluids (SIF, pH = 7.4), and followed a non-Fickian and a Fickian diffusion mechanism, respectively. In vitro release studies showed that its release rate depends on different swelling of the network as a function of the environmental pH and DMAEMA content. SEM micrographs showed homogenous pore structure of the hydrogel with open pores at pH 1.4. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40737.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

The effect of silica addition on the microstructure and properties of polyethylene separators prepared by thermally induced phase separation

Chunjiang Zhang,Yongfeng Xia,Kaihui Zuo,Yu-Ping Zeng

Novel composite polyethylene (PE) separators were prepared via thermally induced phase separation using SiO 2 as the inorganic dopant and dioctyl phthalate as solvent. Through the control of silica content, the microstructure, thermal and crystalline properties, electrolyte uptake, thermal stability, and mechanical properties of the as-prepared separators were investigated. The results showed that the doped silica particles favored the formation of the large pore size. The crystalline degree of PE was enhanced when doping silica in the ternary system below 3 wt %. The liquid electrolyte uptake was increased from 30.2% to 63.2% with doping silica content at 5 wt % in the mixed system, which benefits from the large pore size structure and the hydrophilicity of silica. The thermal decomposition temperature of the composite PE separators is 40°C higher than the pure PE separator due to the steric stabilization and the more stable space structure induced by the doped silica. The tensile strength was increased from 12 MPa to 13.3 MPa when doping 1 wt % silica, but decreased with further silica addition. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40724.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

Effect of diisocyanate on pyridine containing shape memory polyurethanes based on N,N-bis(2-hydroxylethyl)isonicotinamide

Hongming Yuan,Zaochuan Ge,Shaojun Chen,Shiguo Chen,Haipeng Yang,Haitao Zhuo

This article demonstrates a comparative investigation about the effect of diisocyanate on pyridine containing shape memory polyurethanes (Py-SMPUs), which are synthesized with N , N -bis(2-hydroxylethyl)isonicotinamide (BINA) and four different diisocyanates: 1,6-hexanediisocyante (HDI), isophorone diisocyanate (IPDI), methylene diphenyl diisocyanate (MDI), and tolylene diisocyanate (TDI). Results show that all BINA–SMPU systems have amorphous reversible phase. Comparatively, the MDI–BINA and TDI–BINA systems show higher T g ; and the HDI–BINA and IPDI–BINA systems show better thermal stability. In addition, the HDI–BINA and the IPDI–BINA systems exhibit good thermal-induced shape memory effect and good moisture-sensitive shape memory effect due to their better moisture absorption properties. Particularly, the HDI–BINA system has better response speed and better shape recovery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40721.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

Synthesis of a poly(methyl methacrylate)-b-poly[2-(N,N-dimethylamino) ethyl methacrylate] block copolymer and its effects on the surface charges and pH-responsive properties of poly(vinylidene fluoride) blend membranes

Chun-Hui Du,Xu-Min Ma,Chun-Jin Wu,Mei-Qiang Cai,Li-Guang Wu

A poly(methyl methacrylate) (PMMA)- b -poly[2-( N,N -dimethylamino) ethyl methacrylate] (PDMAEMA) block copolymer was successfully synthesized by a reversible addition–fragmentation chain-transfer method. The resulting copolymer was used to prepare poly(vinylidene fluoride) blend membranes via a phase-inversion technique. The polymorphism, structure, and properties of the blend membranes were investigated by Fourier transform infrared spectrometry, scanning electron microscopy (SEM), ζ potential analysis, and filtration. The results indicate that PMMA- b -PDMAEMA could migrate onto the surface of the membrane during the coagulation process, and more of the β-crystal phase appeared with the increase of the block copolymer in the membranes. The surface morphology and cross section of the membranes were also affected by the copolymer, as shown by SEM. The ζ-potential results show that the surface charges of the membrane could be changed from positive to negative at an isoelectric point as the pH increased. The blend membrane also exhibited good pH sensitivity, and its water flux showed a great dependence on pH. The filtration experiment also indicated that the blend membrane had good hydrophilicity and antifouling properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40685.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

Designed magnetic multilayer thin films fabricated via the layer-by-layer assembly of polycyanofullerenes

Jin Luo,Yanhua Wang,Rong Ren,Weilin Sun,Zhiquan Shen

The layer-by-layer self-assembly technique was used to fabricate a series of multilayer thin films with poly[4′-(4-methacryloyphenyl)-2,2′:6′,2″-terpyridine] (PmPhtpy), polycyanofullerenes, and transition metals (Ni 2+ and Co 2+ ). The polymer PmPhtpy was prepared by free-radical polymerization, and this was confirmed by Fourier transform infrared (FTIR) and 1 H-NMR spectroscopy. The polycyanofullerenes, which were characterized by FTIR, ultraviolet–visible (UV–vis), and 13 C-NMR spectroscopy, was synthesized via the bromination of fullerene and then substitution with a nucleophilic reagent [potassium cyanide (KCN)]. The optical properties of the films were measured by attenuated total reflection infrared and UV–vis spectroscopy, and the results indicate that the driving force of the fabrication of the multilayer film was the coordination interaction. The magnetic behavior was examined as a function of the magnetic field strength at 5 K and the temperature (5–300 K). The magnetic hysteresis loops of the films showed a typical S shape at 5 K; this suggested soft ferromagnetic properties. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40681.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 17 · IF 1.64

Preparation of a new superhydrophobic nanofiber film by electrospinning polystyrene mixed with ester modified silicone oil

Yan Song,Lige Wang,Xiuling Wang,Kun Bian,Qingbiao Yang,Yaoxian Li

A new superhydrophobic nanofiber membrane with certain mechanical strength was prepared by electrospinning the polystyrene (PS) with ester modified silicone oil (EMSO). To increase the roughness and tensile strength, the EMSO with low energy as hydrophobic macromolecular substance was added into PS precursor solution. Then during the process of electrospinning, some of the ester modified silicone oil was distribution on the surface of substrate (PS) fiber films to generate double structure which leaded to the superhydrophobicity. We probed into the relationship between the surface wettability, morphologies, mechanical property, and the mass ratios of ester modified silicone oil /PS, and with the increasing of EMSO, the water CA value increased from 135 ± 0.5° to 152 ± 0.2°and the tensile strength grown from 0.23 MPa to 0.92 MPa. The film shows a network structure consisting of numerous randomly oriented fibers, the diameters of which changed from 0.5 μm to 2.0 μm belong to relatively big diameter fibers, which has great significance to the research of superhydrophobic membrane with big diameter fibers and also this method is easy, convenient and environment friendly. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40718.

CAS / MDL: 18497-13-7 111-64-8
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 16 · IF 1.64

Hybrid polydiacetylene/magnetite nanoparticles: Sensing for sodium cetyltrimethylammonium bromide and streptavidin

Shengguo Lu,Fang Luo,Xujia Duan,Chen Jia,Yuwang Han,He Huang

Hybrid nanoparticles composed of polydiacetylene (PDA) and magnetite (Fe 3 O 4 ) were fabricated by a double-emulsion method. The structure and composite form of the hybrid nanoparticles were investigated with transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectroscopy, and dynamic light scattering. The successful incorporation of magnetism to an attractive class of colorimetric PDA sensors was demonstrated. Compared with the PDA vesicles, the hybrid nanoparticles showed better colloidal stability with ethanol stimuli. In this study, we explored the colorimetric sensing ability of the hybrid nanoparticles in response to sodium cetyltrimethylammonium bromide (CTAB). The results show a high sensitivity to CTAB with a limit of detection at 30 μM. The biotin–streptavidin interaction was used as a sensing model to test ligand–receptor interactions on the hybrid nanoparticles' response. The concentration dependence of the chromic response was observed with the limit of visual detection at 20 μg/mL. The Fe 3 O 4 –PDA hybrid nanoparticles might have great potential applications in biosensing because of their advantages, including separation and sensing. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40634.

CAS / MDL: 58-85-5 9013-20-1
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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 16 · IF 1.64

Molecularly imprinted electrochemical sensor for the determination of ampicillin based on a gold nanoparticle and multiwalled carbon nanotube-coated pt electrode

Shoulian Wei,Yong Liu,Tao Hua,Ling Liu,Hongwu Wang

A novel molecularly imprinted electrochemical sensor was developed for the sensitive and selective determination of ampicillin (AMP). The sensor was prepared on a platinum electrode modified with multiwalled carbon nanotubes (MWCNTs), gold nanoparticles (AuNPs), and a thin film of molecularly imprinted polymers (MIPs). MWCNTs and AuNPs were introduced to enhance the sensor's electronic transmission and sensitivity. The molecularly imprinted polymer (MIP) was synthesized using AMP as the template molecule, methacrylic acid as functional monomer, and ethylene glycol maleic rosinate acrylate (EGMRA) as cross-linker. The performance of the proposed imprinted sensor was investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS). The results showed that the imprinted film displayed a fast and sensitive response to AMP. Under optimal conditions, response peak current had a linear relationship with the concentration of AMP in the range of 1.0 × 10 −8 mol/L to 5.0 × 10 −6 mol/L and a detection limit of 1.0 × 10 −9 mol/L ( S/N = 3). This imprinted sensor was used to detect AMP in food samples with recoveries of 91.4–105%. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40613.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2014 ·Vol. 131 ·期 16 · IF 1.64

Star-shaped POSS–methacrylate copolymers with phenyl–triazole as terminal groups, synthesis, and the pyrolysis analysis

Xiu Qiang,Fang Chen,Xiao-Yan Ma,Xian-Bing Hou

Star-shaped polyhedral oligomeric silsesquioxane (POSS)–methacrylate hybrid copolymers with phenyl–triazole as terminal groups had been designed and synthesized via sequential atom transfer radical polymerization (ATRP), azidation, and phenylacetylene-terminated procedures, and the hybrid copolymers here could be denoted as POSS–(PXMA-Pytl) 8 , where X can be M, B, L, and S, represented four different methacrylate monomers, such as methacrylate (MMA), butyl methacrylate (BMA), lauryl methacrylate (LMA), and stearyl methacrylate (SMA), respectively. Thermal gravimetric analysis (TGA) and in situ Fourier transform infrared spectroscopy (FTIR) were applied for studying the thermal stability and degradation mechanism, and it was found that all of the POSS–(PXMA-Cl) 8 and POSS–(PXMA-Pytl) 8 copolymers exhibited excellent thermal stabilities, which had great potential in heat-resistant material application. Different tendencies of decomposition temperatures at 5% and 10% weight loss ( T 5 and T 10 ) dependent on the side-chain length and terminal group species were investigated respectively. The longer alkyl side chains of the monomers, the lower thermal stabilities, and enhanced T 5 and T 10 were also shown with the introduction of phenyl–triazole groups instead of chlorine groups. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131 , 40652.

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