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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 27 ·期 11 ·1451-1457 · IF 1.823

Synthesis, thermal properties and crystalline morphology of poly(trimethylene terephthalate)/ZnO nanocomposites prepared by dual in situ polymerization

Peng Li,Chenguang Yao,Guisheng Yang

Poly(trimethylene terephthalate)/ZnO nanocomposites were successfully prepared by dual in situ polymerization. Firstly, ZnO nanoparticles were synthesized by a simple polyol method using 1,3-propanediol (PDO) as solvent and stabilizer. Then, PTT/ZnO nanocomposites were prepared by in situ polymerization. The results of Fourier transform infrared spectra showed that PTT molecular chains were grafted to the surface of ZnO nanoparticles. The results of 1 H NMR spectra confirmed that propyl ester molecules (as reaction product) were incorporated into PTT molecular chains. It was found that the intrinsic viscosity and molecular weight of synthesized PTT decreased with the addition of ZnO nanoparticles and the incorporation of propyl ester molecules. TEM results showed that ZnO nanoparticles with particle size of 20 ~ 30 nm were well dispersed and fully distributed in the polymer matrix. Besides, the melting temperatures and crystallization temperature decreased gradually and then increased slightly with the increasing loading of ZnO nanoparticles. Because of the strong interaction between ZnO nanoparticles and PTT matrix, the thermal stability of PTT/ZnO nanocomposites was improved. Interestingly, the results of Polarized Optical Microscopy showed that banded spherulites morphology can be observed in all PTT/ZnO nanocomposite samples. However, at higher loading of ZnO nanoparticles, band spacing became larger and was finally disturbed. Copyright © 2016 John Wiley & Sons, Ltd.

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 28 ·期 3 ·367-372 · IF 1.823

Preparation of fluorescent polyaspartic acid and evaluation of its scale inhibition for CaCO3 and CaSO4

Zhenling Shen,Xin Zhi,Puyu Zhang

Polysuccinimide was synthesized from maleic anhydride and urea. A polyaspartic acid derivative (PASP-Try-SEA) was synthesized from the polysuccinimide with 2 -aminoethanesulfonic acid and tryptophan. The products were characterized by UV, FTIR, 1 H NMR, TGA and PL, respectively. The results showed that the fluorescent chromophore-indolyl groups were successfully incorporated into PASP. The relationship between the fluorescence intensity and the concentration of fluorescent polyaspartic acid (FPASP) is linear with the excitation wavelength of 366 nm and 422 nm. FPASP also showed excellent scale inhibition properties with a scale inhibition rate of 78% achieved for CaCO 3 with a dosage of 9 mg/L and a significantly enhanced scale inhibition effect for CaSO 4 , achieving an inhibition rate of 98%, which were determined using the static scale inhibition method. When FPASP was added to the solution, CaCO 3 and CaSO 4 deposits showed flower patterns with floppy accumulation by scanning electron microscopy. Copyright © 2016 John Wiley & Sons, Ltd.

CAS / MDL: 73-22-3 107-35-7
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 28 ·期 4 ·516-523 · IF 1.823

POSS-based poly(aryl ether sulfone)s random terpolymer linked POSS to the main chain: effect of chemical structure and POSS content on properties

Yanfeng Wei,Qiyang Jiang,Jinmeng Hao,Jianxin Mu

In order to investigate the effect of polyhedral oligomeric silsesquioxane content and the structure-function related on the dielectric property and hydrophobicity, three kinds of poly(aryl ether sulfone)s (PAESs) random terpolymer with different chemistry structure at variable polyhedral oligomeric silsesquioxane content in the main chain are prepared. The structures of PAESs are characterized by infrared (IR), nuclear magnetic resonance (NMR), and wide-angle X-ray diffraction (WXRD) spectra. The results show that the dielectric constant initially increases then decrease to 2.68 at 100%-double-decker silsesquioxane (DDSQ)-PAES(molar content of DDSQ = 100%) at 1 MHz. The contact angle increased to 97.5° at 100%-DDSQ-PAES. While the chemical structure of organic chains also plays an important role on thermostability, dielectric, and hydrophobic properties. The results are discussed and interpreted in detail. Copyright © 2016 John Wiley & Sons, Ltd.

CAS / MDL: 80-05-7 75-54-7
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 28 ·期 12 ·1929-1936 · IF 1.907

Preparation of macroporous hydrophobic materials filled with aligned porous hydrophilic domain via emulsion-templated and unidirectional freezing technique

Yun Zhu,Zhen Lu,Jianding Chen,Shengmiao Zhang

A new class of porous materials, having hydrophobic scaffold embedded with aligned porous hydrophilic domains, was in situ fabricated through combination of emulsion-templated method and unidirectional freezing technique. A water-in-oil high internal phase emulsion (HIPE) was prepared with the mixture of styrene and divinylbenzene as continuous phase and a poly(vinyl alcohol) (PVA) aqueous solution as dispersed phase. After polymerization of the continuous phase and subsequently unidirectional freezing, the dispersed phase, a macroporous poly(styrene/divinylbenzene) embedded with an aligned PVA domain, was obtained. The effects of the polymerization temperature, PVA concentration, and freezing rate on these porous materials were investigated. It was found that the PVA domain size and the aligned channel size were dependent on the polymerization temperature, the PVA concentration, and freezing rate. The fabrication method in this work, combining of unidirectional freezing and emulsion template, not only allows to prepare hydrophobic–hydrophilic polyHIPEs having a sea island structure but also dramatically improves the stiffness and specific surface area of the resulting polyHIPEs. Copyright © 2017 John Wiley & Sons, Ltd.

CAS / MDL: 9002-89-5
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 28 ·期 9 ·1107-1114 · IF 1.907

Hemostasis mechanism and applications of N-alkylated chitosan sponge

Yuchen Huang,Longbao Feng,Yi Zhang,Liumin He,Changyong Wang,Jiake Xu,Jianping Wu,Thomas Brett Kirk,Rui Guo,Wei Xue

Chitosan (CHI) is a versatile biological material that is well known for its hemostatic properties. This preliminary study evaluated several self-assembling hydrophobically modified chitosan (HM–CHI) sponges to determine their efficacy on hemostasis . Fourier transform infrared (FT-IR) spectroscopy was used to determine the successful graft of dodecyl groups onto the nitrogen atoms of CHI molecules. A platelet aggregation assay revealed that HM–CHI accelerated the platelet aggregation rate. Fluorescence spectroscopy showed that the HM–CHI changed the structure of fibrinogen in blood. Activated partial thromboplastin time, prothrombin time, fibrinogen time, and thromboelastographic assays were used to explore the effect of HM–CHI on the autologous blood coagulation pathway. Finally, a hemostatic sponge was made with HM–CHI and freeze-dried zeolite composite film and was applied to the rat femoral artery hemostasis model. A hemostasis time of 86 ± 5 sec was achieved, which was significantly better than the one composed with pure CHI. The experimental results of the HM–CHI hemostatic materials are inspiring and will encourage the research and development of such materials. HM–CHI may be a strong candidate as a safe and effective hemostatic material. Copyright © 2017 John Wiley & Sons, Ltd.

CAS / MDL: 64-19-7
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 28 ·期 12 ·1759-1763 · IF 1.907

Preparation and properties of redox responsive modified hyaluronic acid hydrogels for drug release

Renyi Zhang,Xian Li,Kewen He,Xueying Sheng,Shuang Deng,Yueqin Shen,Guanjun Chang,Xu Ye

A series of oxidized hyaluronic acid (oxi-HA)/3,3′-dithiobis (propionohydrazide) (DTP) redox responsive hydrogels by Schiff base reaction under physiological conditions were designed and prepared. The influence of the concentration of oxi-HA and DTP on rheological properties, equilibrium swelling ratio, and degradation rate were investigated. All oxi-HA/DTP hydrogels exhibited good rheological properties, high equilibrium swelling ratio, low degradation rate, and sustainable drug release properties, and the comprehensive performance of oxi-HA5/DTP6 hydrogel was better than that of others. The redox responsiveness was evaluated by means of degradation and in vitro bovine serum albumin release behavior investigation with the stimulus of different concentration of dithiothreitol as reducing agent. The intelligent hydrogels could be potentially applied in the fields of drug delivery system, tissue engineering, or cell scaffold materials. Copyright © 2017 John Wiley & Sons, Ltd.

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 28 ·期 2 ·214-221 · IF 1.823

Poly(dopamine) assisted epoxy functionalization of hexagonal boron nitride for enhancement of epoxy resin anticorrosion performance

Chunli Zhang,Yi He,Yingqing Zhan,Lei Zhang,Heng Shi,Zhonghao Xu

Hexagonal boron nitride (h-BN) is modified by a simple and green method based on self-oxidation of dopamine and epoxy groups functionalized silane (KH560) grafting. The surface modification and microstructure of h-BN are characterized by Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy and transmission electron microscopy. The poly(dopamine) and epoxy groups not only increase the compatibility of the h-BN and enhance its interaction with epoxy matrix but also exhibit a remarkable superiority in enhancing the anticorrosion performance of epoxy coatings. In addition, the anticorrosion mechanisms of h-BN@PDA-KH560 are tentatively discussed. Copyright © 2016 John Wiley & Sons, Ltd.

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 27 ·期 8 ·1029-1037 · IF 1.823

Synthesis, morphology, and nonisothermal crystallization behavior of poly(trimethylene terephthalate)/poly(propylene glycol) segmented random copolymers

Peng Li,Guisheng Yang

Poly(trimethylene terephthalate)/poly(propylene glycol) (PTT/PPG) segmented random copolymers were synthesized by melt copolycondensation. The weight fraction of PPG blocks was ranged from 12.1 to 33.4 wt%, which was confirmed by 1 H NMR spectroscopy. The result of wide-angle X-ray diffractometer indicated that all copolymers had the same crystal structure of PTT homopolymer at room temperature. At a determined crystallization temperature, ring-banded spherulites could be observed in all copolymers samples, and the band spacing increased with the increase of PPG content. Morphologies of copolymers after nonisothermal crystallization process were strongly depended on the cooling rate. Well-defined ring-banded spherulites can be observed only at moderate cooling (20°C/min), while it was really hard to be observed at too low (2.5°C/min) or too high (by air-quenching) cooling rate. Moreover, the size of spherulites decreased with the increase of cooling rate. Finally, different nonisothermal crystallization kinetics were adopt to analyze this copolymer system, and only the Mo method was suitable to describe this copolymer system. Copyright © 2016 John Wiley & Sons, Ltd.

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2015 ·Vol. 27 ·期 7 ·882-888 · IF 1.757

Mechanical, thermal, and UV-shielding behavior of silane surface modified ZnO-reinforced phthalonitrile nanocomposites

Mehdi Derradji,Noureddine Ramdani,Lin-dan Gong,Jun Wang,Xiao-dong Xu,Zai-wen Lin,Abdelkhalek Henniche,Wen-bin Liu

In the present work, zinc oxide nanoparticles were treated with aminopropyl trimethoxy silane-coupling agent and used as a new kind of reinforcement for a typical high performance bisphenol-A-based phthalonitrile resin. The resulted nanocomposites were characterized for their mechanical, thermal, and optical properties. Results from the tensile test indicated that the tensile strength and modulus as well as the toughness state of the matrix were all enhanced with the increasing of the nanoparticles amount. Thermogravimetric analysis showed that the starting decomposition temperatures and the residual weight at 800°C were highly improved upon adding the nanofillers. At 6 wt% nanoloading, the glass transition temperature and the storage modulus were considerably enhanced reaching about 359°C and 3.7 GPa, respectively. The optical tests revealed that the neat resin possesses excellent UV-shielding properties, which were further enhanced by adding the nanofillers. Furthermore, the fractured surfaces of the nanocomposites analyzed by scanning electron microscope exhibited homogeneous and rougher surfaces compared with that of the pristine resin. Finally, the good dispersion of the reinforcing phase into the matrix was confirmed by a high resolution transmission electron microscope. Copyright © 2015 John Wiley & Sons, Ltd.

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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 28 ·期 6 ·658-664 · IF 1.823

Synthesis and characterization of block and random POSS/fluorinated PAES tricopolymers

Qiyang Jiang,Jinmeng Hao,Yanfeng Wei,Jianxin Mu

Block and random polyhedral oligomeric silsesquioxane (POSS)/fluorinated poly aryl ether sulfone tricopolymers were synthesized using different synthetic strategies to investigate the effect of sequence distribution on their thermal, dielectric, and surface properties. Analyses indicated that all block and random copolymers showed similar growth tendency of water contact angles and T g values, downward tendency of k values with increased content of POSS. The block copolymer displayed higher T g values up to 187°C than random copolymers (173°C) under the same POSS molar percentage, which were highly related to their different sequence distribution. The dielectric constants of the tricopolymers were drastically reduced because of the presence of POSS and fluorine, and the dielectric constant could achieve as low as 2.71 (1 MHz). Besides, sequence distribution has no obvious influence on its surface properties and properties. Meanwhile, the yields of degradation residues of the tricopolymers were significantly improved by the ceramic formation from POSS moieties during thermal decomposition. Copyright © 2016 John Wiley & Sons, Ltd.

CAS / MDL: 97-53-0
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 29 ·期 1 ·337-346 · IF 1.907

Surface modification of boron nitride via poly (dopamine) coating and preparation of acrylonitrile-butadiene-styrene copolymer/boron nitride composites with enhanced thermal conductivity

Guohua Li,Rongfen Xing,Peipei Geng,Zhenxin Liu,Lianqi He,Nongyue Wang,Qingxin Zhang,Xiongwei Qu

A biology-inspired approach was utilized to functionalize hexagonal boron nitride (h-BN), to enhance the interfacial interactions in acrylonitrile-butadiene-styrene copolymer/boron nitride (ABS/BN) composites. The poly (dopamine), poly (DOPA) layer, was formed on the surface of BN platelets via spontaneously oxidative self-polymerization of DOPA in aqueous solution. The modified BN (named as mBN) coated with poly (DOPA) was mixed with ABS resin by melting. The strong interfacial interactions via π-π stacking plus Van der Waals, both derived from by poly (DOPA), significantly promoted not only the homogeneous dispersion of h-BN in the matrix, but also the effective interfacial stress transfer, leading to improve the impact strength of ABS/mBN even at slight mBN loadings. A high thermal conductivity of 0.501 W/(m·K) was obtained at 20 wt% mBN content, reaching 2.63 times of the value for pure ABS (0.176 W/(m·K)). Meanwhile, the ABS/mBN composites also exhibited an excellent electrical insulation property, which can be expected to be applied in the fields of thermal management and electrical enclosure.

CAS / MDL: 51-61-6
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2016 ·Vol. 28 ·期 3 ·353-361 · IF 1.823

Flammability and thermal degradation behavior of ethylene-vinyl acetate/layered double hydroxides/zinc borate composites

Yi Qian,Shaojie Zhou,Xilei Chen

Mg-Al-Fe ternary-layered double hydroxides (LDHs) were synthesized by a calcination-rehydration method using Bayer red mud. The products were characterized using X-ray diffraction and thermogravimetric analysis. The flammability and thermal degradation of ethylene-vinyl acetate/layered double hydroxides/zinc borate (EVA/LDHs/ZB) composites were studied with limiting oxygen index, UL 94, cone calorimeter test, smoke density test, and thermogravimetry-Fourier transform infrared spectrometry. Although limiting oxygen index value of the composites decreased with increasing ZB amount, a suitable addition of ZB can apparently improve the UL 94 rating of the material. The heat release rate of the 5% ZB containing ternary composites decreased compared with the EVA/LDHs composites. It is obtained from smoke density test that ZB could help smoke suppression. The ternary composites possessed a higher thermal stability than the EVA/LDHs composites. Copyright © 2016 John Wiley & Sons, Ltd.

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