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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 31 ·50774 · IF 3.125

High loading boron nitride chemically bonded with silicone rubber to enhance thermal neutron shielding and flexibility of polymer nanocomposites

Jia-Le Li,Quan-Ping Zhang,Xue Liu,Rui-Chao Chen,Wei-Di Xu,Nan Sun,Yin-Tao Li,Wen-Bin Yang,Dui-Gong Xu,Yuan-Lin Zhou

Flexible materials with excellent radiation shielding and flexibility are essential to the personal protective equipments (PPEs) for protecting workers from nuclear radiations. However, it is an enormous challenge to obtain the desired materials since high loading filler in polymer nanocomposites usually promotes radiation shielding while restrains its flexibility. Here, a facile “thiol-ene click” means is applied to chemically bond high loading boron nitride (BN) nanoparticles with silicone rubber (SR) in SR/BN nanocomposites for thermal neutron shielding. Uniform dispersion of BN nanoparticles and good compatibility of interfaces in the nanocomposites with high loading filler lead to increased flexibility instead of decrease. In particular, the nanocomposite with 40 wt% BN displays 911% of elongation at break that is about 50% enhancement to that of neat SR. Furthermore, higher loading BN in the nanocomposites means better thermal neutron shielding. Namely, enhanced thermal neutron shielding and flexibility is achieved at SR/BN nanocomposite with 40 wt% BN. The present work provides a facile strategy towards superior integrated performance of flexible materials for radiation shielding, such as wearable devices.

研究领域: 材料科学 · 核工程 · 化学工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 136 ·期 30 ·47811 · IF 2.188

Robust hydrogel of regenerated cellulose by chemical crosslinking coupled with polyacrylamide network

Biao Yang,Wen-Qiang Hua,Lei Li,Zi-Han Zhou,Ling Xu,Feng-Gang Bian,Xu Ji,Gan-Ji Zhong,Zhong-Ming Li

Regenerated cellulose/polyacrylamide (RC/PAAm) double network (DN) hydrogels are composed of cellulose crosslinked by epichlorohydrin (ECH) and chemical-crosslinked PAAm. The prepared RC/PAAm DN hydrogels present enhanced strength, good shape recovery property, excellent energy dissipation properties, decreased equilibrium water content, and low equilibrium swelling ratio (SR). The compressive strength and modulus of RC/PAAm hydrogel are about 4.3 and 11.5 times compared to that of RC hydrogel, respectively. Intriguingly, the chemical crosslinking between ECH and cellulose chains could increase the distance between cellulose chains. Consequently, the increasing molar ratio of ECH to glucose leads to larger SRs and decreased mechanical strength of the hydrogels. Additionally, higher PAAm contents lead to more densely crosslinked networks, and thus decreasing the SRs and improving the mechanical strength of the hydrogels. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47811.

研究领域: 材料科学 · 化学工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 46 · IF 1.768

Reactive flame retardant with core-shell structure and its flame retardancy in rigid polyurethane foam

Fubin Luo,Kun Wu,Yinwen Li,Jian Zheng,Huilong Guo,Mangeng Lu

With a shell of poly (methyl methacrylate-co-hydroxyl ethyl acrylate) (PMMA-HA), microencapsulated ammonium polyphosphate (MHAPP) is prepared by in situ polymerization. The core-shell structure of the reactive flame retardant (FR) is characterized by Fourier transform infrared (FTIR) and scanning electron microscopy/energy dispersive spectroscopy (SEM/EDS). The results of water leaching rate and water contact angle measurements show that ammonium polyphosphate (APP) is well coated by a hydrophobic shell. Due to the presence of active groups (–OH) and hydrophobic groups (–CH 3 ) in shell, MHAPP exhibits better compatibility, flame retardancy, and water resistance compared with neat ammonium polyphosphate (APP) in rigid polyurethane foam (PU). Compression strength of PU/MHAPP with suitable loading is higher than that of PU/APP and PU, the reason is that the active groups in shell can improve the compatibility of MHAPP in PU composite. From thermal stability and residue analysis, it can be seen that the presence of reactive flame retardant shows positive effect on thermal stability of PU composite at high temperature, results also indicate that MHAPP can promote the carbonization formation efficiency of PU composite during combustion process compared with APP. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 42800.

研究领域: 材料科学 · 高分子化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 26 · IF 1.86

Solid–solid phase-change materials based on hyperbranched polyurethane for thermal energy storage

Xiaosheng Du,Haibo Wang,Yan Wu,Zongliang Du,Xu Cheng

A hyperbranched polyol (HBP) was synthesized with poly(ethylene glycol) (PEG) as the core molecule and 2,2-bis(hydroxymethyl) propionic acid as the chain extender. Then, a series of hyperbranched polyurethane phase-change materials (HP-PCMs) with different crosslinking densities was synthesized with isophorone diisocyanate and HBP as a molecular skeleton and PEG 6000 as a phase-change ingredient. 1 H-NMR, gel permeation chromatography, and Fourier transform infrared spectroscopy confirmed the successful synthesis of the HBP and HP-PCMs. The polarization optical microscopy and wide-angle X-ray diffraction results show that the HP-PCM exhibited good crystallization properties, but the crystallinity was lower than that of PEG 6000. The analysis results from differential scanning calorimetry indicated that the HP-PCMs were typical solid–solid phase-change materials with suitable phase-transition temperatures. In addition, HP-PCM-3, with an appropriate degree of hyperbranched structure, possessed the highest thermal transition enthalpy of 123.5 J/g. Moreover, thermal cycling testing and thermogravimetric analysis showed that the HP-PCMs exhibited good thermal reliability and stability. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45014.

研究领域: 材料科学 · 能源科学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 6 ·48355 · IF 2.188

Preparation of high-performance reverse osmosis membrane by zwitterionic polymer coating in a facile one-step way

Yu Xia,Xiaojun Dai,Jing-Gang Gai

Aiming at preparing high-performance polyamide (PA) reverse osmosis (RO) membrane in a facile and high effective way, the codeposition strategy of dopamine and zwitterionic polymer was first applied to modify PA RO membrane. The noncovalent bonds between dopamine and Poly [2-(Methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (PSPE) act to fix PSPE onto the membrane surface and simultaneously destroy the interaction force between dopamine aggregations so that the modified layer could equably form on the PA layer. PSPE significantly improved the hydrophilicity [the water contact angle (WCA) of S-D-3 is 25.3°] of the modified membrane. And, the smoother surface was noticed on the modified membrane. All of these endow the PSPE/dopamine modified membrane superb water flux (the maximum water flux is 51.86 L m −1 h −1 at 1.6 MPa and 25 °C) and impressive antifouling and anti-adhesion properties to bovine serum albumin (BSA) (protein), sodium dodecyl sulfate (anionic surfactant), and dodecyl trimethyl ammonium bromide (cationic surfactant) with salt retention was well maintained. Notably, in the BSA fouling test, nearly 100% of the flux recovery ratio was achieved. This method is promising to be employed in industrial scale-up production. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 48355.

研究领域: 材料科学 · 环境工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 135 ·期 6 ·45804 · IF 1.86

Effect of polyphenylene sulfide containing amino unit on thermal and mechanical properties of polyphenylene sulfide/glass fiber composites

Hao-Hao Ren,Dong-Xia Xu,Ting Yu,Jia-Chao Yang,Gang Zhang,Xiao-Jun Wang,Jie Yang

Three kinds of high-molecular-weight compatibilizers [copoly(1,4-phenylene sulfide)-poly(2,5-phenylene sulfide amine)] (PPS-NH 2 ) containing different proportions of amino units in the side chain) were synthesized by the reaction of dihalogenated monomer and sodium sulfide via nucleophilic substitution polymerization under high pressure. The intrinsic viscosity of the obtained copolymers was 0.354–0.489 dL/g and they were found to have good thermal performance with melting point ( T m ) of 271.3–281.0 °C and initial degradation temperature ( T d ) of 490.0–495.7 °C. There was an excellent physical compatibility between PPS-NH 2 and the pure industrial PPS. The results of dynamic mechanical analysis and macro- and micromechanical test showed that the selective compatibilizer PPS-NH 2 (1.0) (1.0% mol aminated ratio) can improve the mechanical and interfacial properties of polyphenylene sulfide/glass fiber (PPS/GF) composite. The macro-optimal tensile strength, Young's modulus, bending strength, and notched impact strength of 5%PPS-NH 2 (1.0)/PPS/GF composite raised up to 141 MPa, 1.98 GPa, 203 MPa, and 6.15 kJ/m 2 , which increased 12.8%, 9.4%, 4.1%, and 13.8%, respectively, comparing with the pure PPS/GF composite (125 MPa, 1.81 GPa, 195 MPa, and 5.40 kJ/m 2 , respectively). © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 45804.

研究领域: 材料科学 · 聚合物化学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 136 ·期 48 ·48362 · IF 2.188

Using water-miscible nonionic hydrophobic monomer associating HPAM as drag reducing agent

Xianwu Jing,Youquan Liu,Wei Li,Yuan Xu,Zhiyu Huang

A water-miscible nonionic surfmer (AC-TX100) was synthesized based on Triton X-100 and acryloyl chloride. Then, a terpolymer P(AM/AA/AC-TX100) was synthesized by free radical polymerization in aqueous solution and intended to be used as drag reducing agent (DRA). The DRA was defined to be P(AM 87.32 /AA 12.46 /AC-TX100 0.22 ) according to 1 H NMR and elemental analysis, the molecular weight was 2.12 × 10 6 g/mol according to scattering method. DRA shows excellent performance in drag reduction (DR). The highest DR rate of 76% can be obtained when DRA concentration is 0.023% in fresh water; while in brine containing 3% NaCl, DR rate decreases, and it is necessary to increase the concentration to 0.05% to ensure that DR rate is higher than 70%. SEM and cryo-TEM show that DRA forms a network structure in aqueous solution, and the tightness of this structure has a direct influence on DR performance. Specifically, DRA molecules stretch into the whirlpools generated by water at high flow rates, reducing the quantity and intensity of whirlpools, thereby lowering the energy loss and the friction. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 48362.

研究领域: 高分子化学 · 流体力学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2018 ·Vol. 135 ·期 28 ·46503 · IF 1.901

Hierarchical self-assembly of Y-shaped amphiphilic triblock polyurethane/poly(acrylic acid) complexes: Giant vesicles, vesicles, 3D network, and bulk structures

Shuangquan Lai,Yong Jin,Hanping Li,Xiaopeng Sun,Jiezhou Pan

A simple and effective approach to induce hierarchical self-assembly of Y-shaped amphiphilic triblock polyurethane/poly(acrylic acid) complexes system in aqueous media is reported here. Hydrogen bonding interactions and electrostatic repulsive forces, which can be controlled by regulating the pH condition of complexes solution, were the main driving forces to induce morphological transitions. With the gradual decrease of pH value, a variety of micro-/nanostructures including giant vesicles, small vesicles, multi-layer three-dimensional (3D) porous network structures and “bulk” structures were successively obtained. Among these structures, the micron-scale multi-layer 3D porous network structure formed from block copolymer/homopolymer complexes was rarely reported. Therefore, this research demonstrates that the hierarchical self-assembly of polymers complexes in aqueous media is a viable approach to construct different interesting micro-/nanostructure assemblies, and supplies a new clue for the fabrication of multi-layer 3D porous network structures. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 46503.

研究领域: 材料科学 · 高分子化学 · 纳米技术
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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 46 ·51374 · IF 3.125

Hydrogen bonding induced enhancement for constructing anisotropic sugarcane composite hydrogels

Rongnian Xu,Xiaoduo Zhao,Shuanhong Ma,Zhengfeng Ma,Rui Wang,Meirong Cai,Feng Zhou

Anisotropic hydrogels are appealing with their merits of similar biochemical and structural properties to the biological tissues. However, the mechanical properties of current anisotropic hydrogels need to be further improved. Herein, three kinds of novel anisotropic poly(2-hydroxyethyl methacrylate) (pHEMA), poly(acrylamide) (pAM), and poly(acrylamide-co-acrylic acid) (p[AM-co-AA]) sugarcane composite hydrogels were prepared successfully by filling the hydrogel monomer precursor into porous aligned sugarcane nanofibers network and then performing subsequent free radical polymerization. The hydrogel matrix and sugarcane nanofibers network were combined closely together through hydrogen bonding interaction. The anisotropic sugarcane composite hydrogels exhibit good flexibility and elastic recovery properties upon encountering mechanical crimping and twisting. In typical case, the as-prepared pHEMA sugarcane composite hydrogel can exhibit high anisotropic tensile strength of 2.37 and 0.54 MPa, while differential tear strength of 0.36 and 0.78 N/mm, along the parallel and vertical nanofibers directions. Finally, anisotropic lubrication behaviors were found and investigated systematically for those three kinds of sugarcane composite hydrogels when water was used as lubricant. Our current work proposes a simple and universal strategy for developing bioinspired anisotropic functional composite matters such as artificial skin, flexible sensor, and cartilage lubrication materials.

研究领域: 材料科学 · 生物医学工程
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JOURNAL OF APPLIED POLYMER SCIENCE · 2022 ·Vol. 139 ·期 35 ·e52831 · IF 3.057

Three-dimensional printing hydrogel scaffold with bioactivity and shape-adaptability for potential application in irregular bone defect regeneration

Jing Wang,Meiling He,Meixuan Du,Ce Zhu,Yuling Jiang,Yi Zhuang,Lin Qi,Zheng Liu,Yubao Li,Limin Liu,Ganjun Feng,Danqing Wang,Li Zhang

Complex shaped bone defects that need to be filled are very common in clinic. But after filling, gaps are inevitably left between substitutes and host bone due to the poor conformability of preformed implants, hence hindering bone regeneration. Therefore, based on our previous study, we here used the bioink (named PPG) composed of polyurethane, polyacrylamide, and gelatin with optimized composition ratio to three-dimensionally (3D) print an inorganic/organic composite hydrogel scaffold with self-expandability to fill irregular bone defects and bioactivity to accelerate bone healing through adjusting the content of bioactive ceramic (BC). The results indicated that, the 3D printed BC/PPG scaffold had a rough surface on each fiber; with the incorporation of BC powders, the composite hydrogel scaffolds in swelling experiments could perform a comparable self-adaptability to PPG hydrogel scaffold; the bioactive ions including Ca, Mg, and Si could be released from the composite scaffold and induce the rapid deposition of bone-like apatite. The mechanical tests proved that the BC(10%)/PPG scaffold was the top performer under compression. The in vitro cell assessment illustrated that compared with PPG hydrogel scaffold, the BC/PPG composite scaffolds were more favorable to the proliferation and spreading of bone mesenchymal stem cells (BMSCs).

研究领域: 生物医学工程 · 组织工程 · 材料科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2012 ·Vol. 128 ·期 1 ·89-96 · IF 1.289

Synthesis and characterization of glucosamine modified poly(ethylene glycol) hydrogels via photopolymerization

Qunfang Wang,Li Ren,Caixia Xu,Zhichen Zhai,Jia-an Zhou,Yongchang Yao,Huan Xia,Yingjun Wang

This study presented the synthesis and characterization of glucosamine (GlcN) modified poly (ethylene glycol) (PEG) hydrogels. The chemical structure was characterized by Fourier transform infrared (FTIR) and proton nuclear magnetic resonance ( 1 H NMR) spectroscopy. The morphology of hydrogels was observed by scanning electron microscopy (SEM). The results indicated that GlcN was successfully incorporated into PEG hydrogel network. Moreover, the data of the swelling ratio showed that the ratio of GlcN-modified PEG hydrogels was lower than that of pure poly(ethylene glycol) diacrylated (PEGDA). Biocompatibility of unreacted GlcN monomer and GlcN-modified hydrogels was also evaluated in vitro . Compared with glucosamine hydrochloride, 2 and 5 m M N -acroloyl-glucosamine monomer exhibited no toxicity against bone marrow stromal cells (BMSCs), while with the concentration increased to 10 m M , cell viability appeared to decrease. However, when BMSCs were encapsulated in GlcN-modified hydrogels via photopolymerization method, cells remained vigorous viability. Metabolic activity of the encapsulated cells demonstrated GlcN-modified hydrogels was favorable for cell proliferation. Compared with free GlcN, covalent binding GlcN showed lower cytotoxicity and higher cell proliferation properties. As a result, GlcN-modified PEGDA hydrogels could be used as safe and injectable cell carriers for in situ tissue engineering applications. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

研究领域: 生物材料 · 组织工程 · 医学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 8 ·48387 · IF 2.188

Preparation of electrospun nanofibrous polycaprolactone scaffolds using nontoxic ethylene carbonate and glacial acetic acid solvent system

Yu Zhang,Ismat Ullah,Wancheng Zhang,Hao Ou,Marco Domingos,Antonio Gloria,Jinge Zhou,Wenchao Li,Xianglin Zhang

In recent years, solution electrospinning has attracted the interest of researchers due to the possibility to design nanofibrous scaffolds with large surface area to volume ratios. Polycaprolactone (PCL), because of its biocompatibility and easy processability, has been widely used to develop electrospun structures for tissue engineering. However, the use of organic solvents and the poor PCL solution stability still hinder the development of the solution electrospinning process. The relatively benign glacial acetic acid (GAC) as a solvent of PCL was used to fabricate microfibrous fibers or beaded fibers. Thus, ethylene carbonate (EC) as a nontoxic assistant solvent was added to the PCL/GAC solution to successfully fabricate electrospun nanofibrous PCL scaffolds. The stability of the PCL/GAC/EC solution system was demonstrated as the viscosity, which showed no significant change during 48 h. The ultrafine PCL fiber diameter decreased as EC concentration was increased from 0 to 9 vol% and started to slightly increase when EC concentration increased beyond 9 vol%. MTT assay evidenced that MC3T3-E1 cells on the nanofibrous PCL scaffolds exhibited a better enhancement on cell proliferation. In summary, EC was added in PCL/GAC to establish a stable and low toxic solution electrospinning system, which provides promising strategy in tissue engineering field. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 48387.

研究领域: 生物材料学 · 组织工程学
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