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Journal of Materials Chemistry A · 2014 ·Vol. 2 ·期 26 ·10169-10181 · IF 0

Development of supramolecular liquid-crystalline polyurethane complexes exhibiting triple-shape functionality using a one-step programming process

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

Supramolecular liquid crystalline polymers and shape memory polymers are attracting increasing interest as materials. In this paper, we describe the development of a supramolecular liquid crystalline shape memory polyurethane (SLCSMPU) complex that exhibits both liquid crystalline properties and shape memory properties. The complex is formed by incorporating 4-hexadecyloxybenzoic acid (HOBA) into a pyridine-containing shape memory polyurethane (PySMPU). The HOBA is tethered to the PySMPU by strong hydrogen bonding between the pyridine rings and the COOH of the HOBA, forming a SLCSMPU complex. Heat treatment plays an important role in the formation of hydrogen-bonded supramolecular liquid crystalline structures in these SLCSMPU complexes. Thus, the SLCSMPU complex not only maintains the intrinsic liquid-crystalline properties of HOBA, but can also form a stable polymeric film for various shape memory applications. Additionally, the SLCSMPU complex forms a two-phase separated structure composed of an amorphous polyurethane matrix and a HOBA crystalline phase, which includes the hydrogen-bonded crystalline HOBA phase and the free HOBA crystalline phase. Therefore, a simple one-step programming process is developed that produces SLCSMPU complexes with excited triple-shape functionalities due to their multiple phase transitions, especially when the molar ratio of HOBA/BINA is less than 0.8.

研究领域: 高分子科学 · 材料化学 · 软物质物理 · 智能材料 · 功能高分子
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DESALINATION · 2012 · IF 2.59

Carboxylate-terminated double-hydrophilic block copolymer as an effective and environmental inhibitor in cooling water systems

Lei Ling,Yuming Zhou,Jingyi Huang,Qingzhao Yao,Guangqing Liu,Peixin Zhang,Wei Sun,Wendao Wu

In an attempt to control Ca 3 (PO 4 ) 2 , CaCO 3 , and CaSO 4 deposits in industrial recycling water systems, an acrylic acid (AA)-allyloxy poly(ethylene glycol) polyglycerol carboxylate (APEG-PG-COOH) copolymer was synthesized as a nonphosphorus inhibitor. The synthesized polymer was characterized by 1 H NMR. The performance of PAA/APEG-PG-COOH on inhibition of Ca 3 (PO 4 ) 2 , CaCO 3 and CaSO 4 precipitation was studied through static scale inhibition tests. It was shown that PAA/APEG-PG-COOH exhibited excellent ability to control inorganic minerals, with approximately 100% CaSO 4 inhibition and 99.89% Ca 3 (PO 4 ) 2 inhibition at levels of 3 and 6   mg/L PAA/APEG-PG-COOH, respectively. PAA/APEG-PG-COOH also displayed ability to prevent the formation of CaCO 3 scales. The effects on formation of Ca 3 (PO 4 ) 2 , CaCO 3 and CaSO 4 were investigated with combination of Scanning electronic microscopy (SEM), Transmission electron microscopy (TEM), and X-ray powder diffraction (XRD) analysis, respectively.

研究领域: 环境化学 · 材料科学 · 工业水处理 · 高分子化学 · 腐蚀与防护 · 矿物结垢控制
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2016 ·Vol. 134 ·期 1 · IF 1.866

Synthesis of cis-1,4-polyisoprene with Al-Ti catalysts modified by different electron donor reagent

Zhaowei Wang,Zhixia Wen,Xing Li,Junwei Yu,Xiaoxuan Liu

The preparation of the high cis −1,4-polyisoprene by Ziegler-Natta catalysis system was studied. The effect of Al-Ti catalysts modified by ethers with different structures which are different electron donor reagent on polymerization of isoprene has been mainly investigated. By the measurement method of the monomer conversion, FTIR, and 1 H NMR spectroscopy, the influence of, respectively, added diphenyl ether, anisole, dibutyl ether, or methyl tert -butyl methyl ether as a third active component on the heterogeneous TiCl 4 -Al( i -Bu) 3 -ether catalyst activity and microstructure of synthetic polyisoprene was analyzed. By the adding of diphenyl ether or dibutyl ether, the process of prefabricated heterogeneous catalyst is quickly and catalyst particle quantity is large. The polymerization conversion is high and the microstructure cis −1,4 content of the resulting polymer can reach 92%. But Al( i -Bu) 3 added anisole or methyl tert -butyl methyl ether hard to cooperate with TiCl 4 . © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 44357.

研究领域: 高分子化学 · 催化化学 · 功能材料 · 合成高分子 · 配位聚合
✓ 已验证 DOI 高影响因子
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PROGRESS IN ORGANIC COATINGS · 2020 · IF 4.469

Phosphorylated polymer/anionic surfactant doped polypyrrole in waterborne epoxy matrix toward enhanced mechanical and chemical resistance

Haihua Wang,Wenjing Zhang,Yongning Ma,Guiqiang Fei,Huan Wen,Liyu Sun,Yanming Shao,Yong-Mook Kang

The compatibility between polypyrrole (PPy) and waterborne epoxy coating (EP) remains the main challenge. Here, phosphorylated poly (vinyl alcohol) (PPVA) and p-toluene sulfonic acid sodium (p-TSA) were simultaneously utilized as dopants to modify PPy and prepare water dispersible PPVA/p-TSA/PPy (PPVAT/PPy) solution. Additionally, poly (vinyl alcohol) (PVA) and TSA were also adopted to prepare PVA/p-TSA/PPy (PVAT/PPy) for comparison. Denser film with granular morphology was observed for PPVAT/PPy nanocomposite film. Compared with PVAT/PPy-40 %, the tensile strength of PPVAT-8.0 %/PPy-40 % increased from 248.8–283.9 MPa. PPVAT/PPy displayed higher compatibility and interactions with EP compared to PPy-TSA and PVAT/PPy. Compared with EP, the impedance modulus of PVAT/PPy+EP and PPVAT/PPy+EP increased from 3.17×10 5 to 1.07×10 8 and 1.62×10 9 Ω·cm 2 ; corrosion current density I corr decreased from 1.49×10 −6 to 7.72×10 -8 and 4.01×10 -9 A·cm -2 ; corrosion potential E corr displayed a positive shift of 230 mV and 269 mV, respectively. The corrosion inhibition efficiency of PPVAT/PPy+EP reached 99.83 %, which is much higher than that of PVAT/PPy+EP (93.97 %). PPVAT/PPy+EP nanocomposite coating has been proved to have preferable long-term corrosion resistance based on electrochemical impedance spectra (EIS), polarization curves and salt water spray test. The simultaneous incorporation of phosphate anions, sulfate ions and PPy into EP was beneficial to fabricate high-performance anticorrosion coating.

研究领域: 材料科学 · 高分子化学 · 腐蚀防护 · 纳米复合材料 · 表面工程
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

A multifunctional nano filler for solid polymer electrolyte toward stable cycling for lithium-metal anodes in lithium–sulfur batteries

XinLong Zhang,HaiYan Zhang,Yuan Geng,ZhangQin Shi,Sheng Zhu,QunJie Xu,YuLin Min

Lithium–sulfur (Li–S) batteries are considered as very promising energy storage systems due to their higher theoretical performance and lower active material cost. However, the notorious shuttle effect and lithium dendrite growth have severely restricted the industrial production of Li–S batteries. In this study, we used polyethylene oxide (PEO) as the matrix and added multifunctional nanofillers (nano In 2 O 3 ) to effectively inhibit the shuttle effect caused by the dissolution of lithium polysulphides (LiPSs) in Li–S batteries. As a multifunctional filler, nano-In 2 O 3 not only improves the ionic conductivity of the PEO electrolyte, but also forms a Li–In alloy layer in situ at the polymer/anode interface, which can cause the rapid diffusion of lithium ions and prevent the side reactions between lithium metal anode and the electrolyte. Achieving the effect of stabilizing the lithium metal anode and suppressing the shuttle effect. Multiple problems in the system are solved by introducing a single component with multiple functions. The symmetrical lithium battery based on the PEO/LiTFSI/In 2 O 3 solid polymer electrolyte (PEO/LiTFSI/In 2 O 3 SPE) has higher cycle stability (over 1200 h) because it is more stable to the lithium metal anode. The Li–S full battery also exhibits excellent electrochemical performance. After 500 cycles at 1C, its capacity can be maintained at 570 mAh g −1 , the capacity decay rate is 0.038%. The coulombic efficiency (CE) during the cycle is also close 100%.

研究领域: 电化学 · 能源材料 · 固态离子学 · 电池技术 · 纳米复合材料
✓ 已验证 DOI 高影响因子
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Plasma Processes and Polymers · 2011 ·Vol. 8 ·期 10 ·923-931 · IF 1.643

Plasma Polymerized Pyrrole Films for Biological Applications: Correlation Between Protein Adsorption Properties and Characteristics

Zhihong Zhang,Jun Dou,Fufeng Yan,Xianjun Zheng,Xili Li,Shaoming Fang

The present work describes the fabrication, characterization, and optimization of plasma polymerized pyrrole films, PPpy, prepared by continuous wave for application as the adhesion layers of bovine serum albumin (BSA). Plasma conditions used throughout the work produced significant differences in the chemical, physical, and electrochemical properties of the resultant PPpy films. Structural analysis and property characterizations of PPpy were carried out using Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and electrochemical workstation. Surface plasmon resonance spectroscopy was used to investigate the adsorption kinetics of BSA onto PPpy films. Moreover, when immersed in solutions or after BSA adsorption, the differences of electron transfer at the interfaces between the PPpy and the electrolyte solutions were determined by electro impedance spectroscopy. While there is a clear dependence of the protein adsorption affinity on the plasma polymerization condition employed during the film preparation. The relationship between film structure, electrochemical properties, polymer stability in aqueous buffer, and protein binding affinities are discussed.

研究领域: 生物材料 · 表面科学 · 生物医学工程 · 分子生物学 · 分析化学 · 生物传感器
✓ 已验证 DOI 高影响因子
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Food Analytical Methods · 2015 ·Vol. 9 ·期 7 ·2026-2035 · IF 1.956

A Novel Molecularly Imprinted Polymer Based on Carbon Nanotubes for Selective Determination of Dioctyl Phthalate from Beverage Samples Coupled with GC/MS

Du Jiaojiao,Gao Ruixia,Mu Hui

Phthalates represent a potential risk for humans, since they are ubiquitous environmental contaminants. Efficient extraction and purification procedures are demanded for the detection of low concentration levels of phthalates. In this work, a novel type of molecularly imprinted polymers coated onto the surface of vinyl functionalized multi-walled carbon nanotubes was synthesized and coupled with gas chromatography–mass spectrometry (GC/MS) for the selective separation and determination of dioctyl phthalate (DOP) in beverage samples. The morphology, structure property, and thermostability of the resultant polymers were characterized by transmission electron microscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The adsorption properties of the prepared polymers were investigated by equilibrium rebinding and competitive experiments. The resultant imprinted nanomaterials exhibited high capacity and favorable selectivity. In addition, the feasibility of the developed method using the obtained imprinted polymers as a solid-phase sorbent coupled with GC/MS for the selective isolation and determination of DOP in different beverage samples was demonstrated. Under optimal conditions, the limit of detection of the proposed method for DOP was 2.3 ng L −1 . DOP spiked at three levels of concentration in beverage samples was extracted and determined through the application of the present method, with recoveries ranging from 88.6 to 93.0 % with relative standard deviations less than 5.6 %.

研究领域: 分析化学 · 环境毒理学 · 食品安全 · 分子识别 · 材料科学 · 色谱分析
✓ 已验证 DOI 高影响因子
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Materials Today Energy · 2022 · IF 9.257

Improvement of high-temperature energy storage performance in polymer dielectrics by nanofillers with defect spinel structure

Jing Fu,Mingcong Yang,Rui Wang,Sang Cheng,Xiaoyan Huang,Shaojie Wang,Junluo Li,Manxi Li,Jinliang He,Qi Li

The electrostatic energy storage performance of polymer dielectrics at high temperature and high electric field can be significantly improved by the incorporation of wide-bandgap, nano-sized particles. It is traditionally believed that the embedded nanoparticles can scatter the hot charges and lead to charge trapping in the interfacial region , which suppress the conduction loss and promote the energy storage performance. In this work, the nano-sized γ-Al 2 O 3 with cubic defect spinel structure and nano-sized α-Al 2 O 3 with a wider bandgap are introduced into a heat-resistant dielectric polymer, respectively, to form two different nanocomposites . The field-dependent energy storage performance, electrical conductivity , and breakdown strength of the polymer nanocomposites at high temperatures, as well as the thermally stimulated depolarization current , are investigated. The results indicate that the intrinsic deep traps introduced by γ-Al 2 O 3 with cubic defect spinel structure are a more critical factor in improving the energy storage performance of the polymer-based composites. We anticipate that our findings reported in this work may help to better guide the selection of nanofillers for high-temperature dielectric polymer nanocomposites.

研究领域: 材料科学 · 介电物理 · 高分子物理 · 能源材料 · 电气工程
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POLYMERS FOR ADVANCED TECHNOLOGIES · 2017 ·Vol. 28 ·期 11 ·1464-1472 · IF 1.907

Study on the moisture absorption of zwitterionic copolymers for moisture-sensitive shape memory applications

Zhankui Mei,Huanhuan Ren,Shaojun Chen,Zaochuan Ge,Jinlian Hu

This study develops a new type of moisture-sensitive shape memory polymer based on zwitterionic copolymers synthesized with acrylic acid (AA) and 3-Dimethyl (methacryloyloxyethyl) ammonium propane sulfonate (DMAPS). The moisture absorption properties of zwitterionic copolymers are particularly investigated in this paper. The results demonstrate that the DMAPS/AA copolymers possess a sulfobetaine structure and form a two-phase separation structure. The zwitterionic copolymers show both good hydrophilic properties and moisture absorption properties. Both AA and DMAPS segments influence the hydrophilic properties and moisture absorption of the composite copolymer. The moisture absorption process is well modeled by Fick's second law in its initial stage. The moisture absorption is mainly determined by immersion conditions and the given materials' structure. Moisture absorption speed and saturated moisture absorption both increase with an increase in DMAPS content as well as the immersion temperature. The increased moisture absorption rate and higher saturated moisture absorption results from the higher activation energy of diffusion. The DMAPS/AA copolymers demonstrate adequate moisture-sensitive shape memory effects. Stain recovery is faster in the zwitterionic copolymers containing higher DMAPS content, whereas the final shape recovery decreases with an increase of DMAPS content. Finally, it is proposed that not only good moisture absorption units are required but also physical crosslinks should be improved for moisture-sensitive shape memory polymers. Copyright © 2017 John Wiley & Sons, Ltd.

研究领域: 高分子材料科学 · 功能高分子 · 智能响应材料 · 生物医用材料 · 软物质物理 · 环境响应材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2022 · IF 9.794

Interfacial water distribution behaviors in high performance bipolar membrane fuel cell

Zhengjian Li,Sian Chen,Liting Cui,Haining Wang,Shanfu Lu,Yan Xiang

The acidic-alkaline interface of a bipolar membrane fuel cell (BPMFC) is the place to generate water, which significantly affect the output performance of BPMFC by regulating the water distribution due to the ion conductivity and oxygen reduction reaction (ORR) kinetics in cathode. To investigate the influence of water diffusivity ( D w ) on the water distribution, four alkaline polymer electrolytes with different D w is selected as anion exchange membrane or alkaline electrolyte ionomer to assemble BPMFCs. A combined experimental and simulated study reveals the positive correlation relationship of D w to the water distribution and performance of BPMFC. By increasing the D w of the alkaline polymer electrolytes, the interfacial-generated water amount can be increased and promptly transport to the cathode, thereby satisfying the ion conductivity and increasing the ORR kinetics, and breakthrough the peak power density of the BPMFC with 1.06 W cm −2 without humidification .

研究领域: 电化学 · 能源材料 · 燃料电池 · 高分子科学 · 界面科学
✓ 已验证 DOI 高影响因子
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EUROPEAN POLYMER JOURNAL · 2015 · IF 3.005

Thermo-sensitive drug controlled release PLA core/PNIPAM shell fibers fabricated using a combination of electrospinning and UV photo-polymerization

Hongwei Zhang,Qijian Niu,Ning Wang,Jun Nie,Guiping Ma

In this research a thermo-sensitive drug loaded core–shell fibers were prepared by UV photo-polymerization combined with electrospinning technology. The biodegradable polymer polylactic acid (PLA) was used as the core with electrospinning and the N-isopropylacrylamide (NIPAM) was selected to be shell of the fibers via UV photo-polymerization, respectively. Combretastatin A4 (CA4) was used as the model drug loaded in PLA (core structure) to test the thermo-sensitivity of the core–shell fibers. SEM was performed to observe the morphology of the fibers. TEM was carried out to confirm the core–shell structure of the fibers. Furthermore, XPS and FTIR results demonstrated that the core–shell structure had been fabricated as designed. Water contact angle (WCA) test indicated that the fibers show different wettability when the temperature was below or above the lower critical solution temperature (LCST). Moreover, in vitro drug release test was conducted to explore the difference of the drug release when the temperature was at 25   °C and 40   °C. The cell culture studies showed that the prepared core–shell structure nanofibers have a potential application in the biomedical fields as tissue engineering.

研究领域: 生物材料 · 药物递送 · 组织工程 · 高分子科学 · 纳米医学
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Small · 2018 ·Vol. 14 ·期 34 ·1801798 · IF 9.598

Flexible, Flame-Resistant, and Dendrite-Impermeable Gel-Polymer Electrolyte for Li–O2/Air Batteries Workable Under Hurdle Conditions

Xiaohong Zou,Qian Lu,Yijun Zhong,Kaiming Liao,Wei Zhou,Zongping Shao

Gel-polymer electrolytes are considered as a promising candidate for replacing the liquid electrolytes to address the safety concerns in Li–O 2 /air batteries. In this work, by taking advantage of the hydrogen bond between thermoplastic polyurethane and aerogel SiO 2 in gel polymer, a highly crosslinked quasi-solid electrolyte (FST-GPE) with multifeatures of high ionic conductivity, high mechanical flexibility, favorable flame resistance, and excellent Li dendrite impermeability is developed. The resulting gel-polymer Li–O 2 /air batteries possess high reaction kinetics and stabilities due to the unique electrode–electrolyte interface and fast O 2 diffusion in cathode, which can achieve up to 250 discharge–charge cycles (over 1000 h) in oxygen gas. Under ambient air atmosphere, excellent performances are observed for coin-type cells over 20 days and for prototype cells working under extreme bending conditions. Moreover, the FST-GPE electrolyte also exhibits durability to protect against fire, dendritic Li, and H 2 O attack, demonstrating great potential for the design of practical Li–O 2 /air batteries.

研究领域: 电化学能源 · 材料科学 · 纳米复合材料 · 先进电池技术 · 固态离子学
✓ 已验证 DOI 高影响因子
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