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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 132 ·期 17 · IF 1.768

Bifunctional cellulose derivatives for the removal of heavy-metal ions and phenols: Synthesis and adsorption studies

Ronglan Wu,Lingyuan Tian,Wei Wang,Xiaolin Man

In this article, we report a study of the design and synthesis of a bifunctional cellulose derivative on the removal of phenols and heavy-metal ions in wastewater treatment. A radical polymerization was performed in an ionic liquid, 1-allyl-3-methylimidazolium chloride, to graft two monomers, butyl methacrylate and 4-vinyl pyridine, on the backbone of cellulose. The effects of the five reaction conditions on the yield of final products were evaluated. The grafted celluloses were characterized by means of Fourier transform infrared spectroscopy, scanning electron microscopy, and thermogravimetric analysis. Adsorption experiments were carried out on the cellulose- g -poly(butyl methacrylate- co -4-vinyl pyridine) to evaluate the capacity of the removal of 2,4-dichlorophenol (2,4-DCP) and Cu(II) in water. The adsorption isotherms were measured at five temperatures and interpreted by a Langmuir model of adsorption. The thermodynamics of the adsorption suggested that the binding process was mildly exothermic for Cu(II) and endothermic for 2,4-DCP. Kinetic studies were interpreted with a pseudo-second-order adsorption model. The process of the adsorption of 2,4-DCP could be described overall by the model, whereas the adsorption of Cu(II) involved two processes. This was due to adsorption both on the surface and inside the adsorbent. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132 , 41830.

研究领域: 环境化学 · 高分子材料科学 · 水处理技术 · 吸附分离 · 绿色化学
✓ 已验证 DOI 高影响因子
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CHEMICAL ENGINEERING JOURNAL · 2017 · IF 6.216

Fabricating an enhanced sterilization chitosan-based flocculants: Synthesis, characterization, evaluation of sterilization and flocculation

Xiang Li,Huaili Zheng,Yili Wang,Yongjun Sun,Bincheng Xu,Chuanliang Zhao

Modified natural polymer flocculants has been the focus of research in environmental engineering field. Natural large molecular compound, chitosan (CTS) with many functional amino and hydroxyl groups can be easily modified to enhance its original functions. This work presents an environmentally friendly chitosan-based cationic polyacrylamide flocculants (CTS-g-PAMA) with enhanced function of sterilization and flocculation . CTS-g-PAMA was synthesized through Ultraviolet (UV)-initiated copolymerization. Structure characterization of FTIR, 1 H NMR, XRD and UV spectrum confirmed the successful grafting of AM and MAPTAC. Scanning electron microscopy (SEM) analysis results showed that CTS-g-PAMA exhibited a porous structure with a prodigious surface area. CTS-g-PAMA was then applied to treat a series of simulated waste water containing kaolin or Escherichia coli . Flocculation tests indicated that CTS-g-PAMA not only showed excellent flocculation effect but also showed high sterilization capability. A series of ONP concentration measurement tests through UV spectra analysis and 3D EEM analysis of suspension before and after flocculation were conducted to study sterilization mechanism, and results revealed the sterilization effect of CTS-g-PAMA was essentially bactericidal, not just antibacterial.

研究领域: 环境工程 · 高分子化学 · 水处理技术 · 材料科学 · 微生物学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2024 ·Vol. 141 ·期 18 ·e55316 · IF 2.7

High-temperature resistant copolymer oil well cement retarder: Synthesis, assessment of performance, and mechanism of retardation

Jifa Bian,Zhongbin Ye,Xuecheng Zheng,Chengwen Deng,Lei Tang

This work used aqueous solution free radical polymerization to create polymers of 2-acrylamide-2-methylpropane sulfonic acid, itaconic acid, and allyl polyoxyethylene ether as a high-temperature resistant retarder (APMS/IA/APEG, from now on referred to as AIA). Gel permeation chromatography, fourier transform infrared (FTIR), proton nuclear magnetic resonance ( 1 HNMR), and thermo-gravimetric analysis (TG) were used to characterize their molecular structure and characteristics. Tests were conducted on the thickening time, rheological characteristics, and compressive strength of AIA in cement slurries. The cement slurry thickened for 276 min at 180°C during the test, and the cement stone's 24-h compressive strength was consistently more than 20 MPa. The hydration products were analyzed using x-ray diffractometer and scanning electron microscopy methods, which were then coupled with molecular dynamics simulations to elucidate the AIA retarding mechanism. When AIA is added to a cement slurry, it forms a chelate structure with Ca 2+ and a strong adsorption layer on the surfaces of the cement particles. This stops the cement from hydrating. The AIA side chain, APEG, can wrap the active group in AIA at low temperatures. AIA exposes more adsorption groups because of the APEG chains stretching at higher temperatures. AIA can, therefore, be used for deep well operations at high temperatures.

研究领域: 材料科学 · 石油工程 · 高分子化学 · 水泥化学 · 胶体与界面科学
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF POLYMER SCIENCE · 2015 ·Vol. 33 ·期 7 ·976-987 · IF 1.835

Enhanced ultraviolet resistance of polypropylene random copolymer filled by ZnO-supported mesoporous zeolite

Li Mei,Li Gu,Zhang Zi-shou,Dai Xin,Yang Yue-wen,Mai Kan-cheng

To enhance the ultraviolet resistance of ZnO based polymer materials, ZnO-supported mesoporous zeolite (M-ZnO) was prepared and characterized by atomic absorption spectroscopy and scanning electron microscopy. The ultraviolet resistance, crystallization behavior and melting characteristics of ZnO and M-ZnO filled PPR composites were compared by FTIR spectra and differential scanning calorimetry. The ultraviolet resistance of M-ZnO filled PPR composites is higher than that of ZnO filled PPR composites, indicating higher ultraviolet resistance of M-ZnO than that of ZnO. The crystallization temperatures of mesoporous zeolite filled PPR were higher than those of M-ZnO and decreased with increasing UV-irradiation time. But the crystallization temperatures of M-ZnO filled PPR composites were not influenced by UV-irradiation time. The ZnO supported on the surface of zeolite is effective in enhancing the ultraviolet resistance of ZnO based polymer materials.

研究领域: 高分子材料科学 · 功能复合材料 · 材料老化与稳定性 · 纳米复合材料 · 聚合物改性
✓ 已验证 DOI 高影响因子
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MACROMOLECULAR RAPID COMMUNICATIONS · 2015 ·Vol. 36 ·期 15 ·1437-1443 · IF 4.941

Self-Assembly-Driven Electrospinning: The Transition from Fibers to Intact Beaded Morphologies

Linge Wang,Paul D. Topham,Oleksandr O. Mykhaylyk,Hao Yu,Anthony J. Ryan,J. Patrick A. Fairclough,Wim Bras

Polymer beads have attracted considerable interest for use in catalysis, drug delivery, and photo­nics due to their particular shape and surface morphology. Electrospinning, typically used for producing nanofibers, can also be used to fabricate polymer beads if the solution has a sufficiently low concentration. In this work, a novel approach for producing more uniform, intact beads is presented by electrospinning self-assembled block copolymer (BCP) solutions. This approach allows a relatively high polymer concentration to be used, yet with a low degree of entanglement between polymer chains due to microphase separation of the BCP in a selective solvent system. Herein, to demonstrate the technology, a well-studied polystyrene-poly(ethylene butylene)–polystyrene triblock copolymer is dissolved in a co-solvent system. The effect of solvent composition on the characteristics of the fibers and beads is intensively studied, and the mechanism of this fiber-to-bead is found to be dependent on microphase separation of the BCP.

研究领域: 高分子科学 · 纳米材料 · 生物医学工程 · 药物递送 · 组织工程
✓ 已验证 DOI 高影响因子
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CHEMOSPHERE · 2024 · IF 8.1

Fabrication of crown ether-containing copolymer porous membrane and their enhanced adsorption performance for cationic dyes: Experimental and DFT investigations

Meng Wang,Rongkang Yan,Meng Shan,Shasha Liu,Hai Tang

Adsorptive separation membranes are widely utilized for the removal of toxic dyeing pollutants from dyeing wastewater. However, developing novel adsorption membranes with large adsorption capacities and enhanced adsorption performance for dyes in actual wastewater poses a significant challenge. This study focuses on the fabrication of crown ether-containing copolymer porous membrane (CRPM) and investigation of the adsorption performance of dyes from aqueous solutions. The morphology structure and pore size distribution revealed that the membrane was endowed with rich micropores and hierarchical porous structures. Three typical cationic dyes (MB, RhB, CV) and an anionic dye (MO) were selected to evaluate the adsorption behavior. The results of adsorption isotherms and kinetics demonstrated that the adsorption data could be well-fitted using the Freundlich and pseudo-first-order kinetic models, the thermodynamic parameters revealed that the adsorption process of dyes on CRPM is a spontaneous endothermic reaction. The membrane exhibited excellent adsorption performance for cationic dyes, with RhB displaying a higher maximum adsorption capacity than previously reported porous membranes. Notably, dynamic adsorption-desorption filtration demonstrated a rapid removal efficiency, with RhB, MB, and CV achieving removal rates of 99.09%, 98.63%, and 99.14% respectively, after five cycles. The filtration volume of the CRPM membrane was 2.4-fold greater than that of a traditional PVDF membrane when applied to actual dyeing wastewater. DFT theoretical calculations were employed to elucidate the adsorption mechanism. These calculations confirmed the significant roles of electrostatic interactions, H-bonds and π–π interactions in facilitating the high-efficiency adsorption of cationic dyes. These findings highlight the potential of the crown ether-containing copolymer as a promising material for adsorption separation membranes in the treatment of dyeing wastewater.

研究领域: 环境科学 · 材料科学 · 高分子化学 · 分离科学 · 物理化学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2018 ·Vol. 8 ·期 9 ·4604-4609 · IF 2.936

Synthesis of triblock copolymer polydopamine-polyacrylic-polyoxyethylene with excellent performance as a binder for silicon anode lithium-ion batteries

Lei Lü,Hongming Lou,Yinglin Xiao,Guangzhao Zhang,Chaoyang Wang,Yonghong Deng

Triblock copolymer polydopamine-polyacrylic-polyoxyethylene (PDA-PAA-PEO) with excellent performance as a binder for silicon anodes was synthesized. Its structure was confirmed by 1H-NMR, FTIR and UV-vis spectroscopy. Results of electrochemical measurements indicated that a silicon anode based on PDA-PAA-PEO binder exhibited excellent cycle performance with a reversible capacity of 1597 mA h g−1 after 200 cycles at a current density of 0.5 C, much better than that of an electrode based on a polyvinylidene-fluoride binder. Improvement of the cycle performance and reversible capacity for silicon anodes could be attributed to the strong adhesive and high ion conductivity of PDA-PAA-PEO.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 纳米材料 · 电池技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2013 ·Vol. 130 ·期 4 ·2345-2351 · IF 1.395

Micro-gels for impact protection

Chao Zhou,Bo Wang,Fengtao Zhang,Kun Xu,Changyu Han,Hong Hu,Yanpin Liu,Pixin Wang,John H. Xin

A novel kind of impact protective material, named as impact protective micro-gel (IPM), was synthesized via a precipitation copolymerization of a compound containing boron and silanol. Diphenylmethane diisocyanate (MDI) was introduced as the chain extender to enhance its impact protective performance. Its rheological properties and morphology were investigated. Three-dimensional (3D) spacer warp-knitted fabrics were dip-coated with the IPM made with and without use of MDI, and the impact protective performance of 3D finished fabrics was assessed by drop impact tests. The results show that the adjustment of the MDI content can adjust the real cross-linking density of the IPM due to the entanglement of polymer chains, and an appropriate cross-linking density can endow dilatant properties to the IPM samples. The results also show that the impact protective performance of 3D spacer fabrics finished with the IPM can be significantly improved. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2345–2351, 2013

研究领域: 高分子材料科学 · 纺织工程 · 防护材料 · 流变学 · 功能材料
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2012 ·Vol. 129 ·期 2 ·846-852 · IF 1.289

Environmental pH-responsive fluorescent PEG-polyurethane for potential optical imaging

Hong Yu Yang,Xiu Mei Zhang,Li Jie Duan,Ming Yao Zhang,Guang Hui Gao,Hui Xuan Zhang

A series of environmental pH-responsive block copolymers PEG-polyurethane with tertiary amine groups in the main chain and free carboxyl groups in the side chain were synthesized, including poly(ethylene glycol) (PEG), 1,4-bis (hydroxyethyl) piperazine, 1,6-diisocyanato hexamethylene, and 2,2-dimethylolpropionic acid. The chemical structure, molecular weight, and pH-dependent capacity of pH-responsive PEG-polyurethane were examined by 1 H-NMR, FTIR, gel permeation chromatography (GPC), and an acid-base titration. Moreover, the fluorescent dye fluorescein isothiocyanate was conjugated with PEG-polyurethane by the similar polymerization method and the obtained polymer was measured by ultraviolet visible spectroscopy (UV-vis) and fluorescent spectroscopy. The results indicated that the pH-responsive PEG-polyurethane showed a pH-buffering phenomenon and fluorescent imaging in a range of pH values. As a result, we demonstrated its potential application for optical imaging; however, it is believed that more applications in the areas of biomedicine will be possible owing to its free carboxyl acid terminal residues in the stimuli-responsive polymer. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013

研究领域: 生物材料 · 分子影像学 · 高分子化学 · 纳米医学 · 药物递送 · 生物传感器 · 转化医学
✓ 已验证 DOI 高影响因子
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MACROMOLECULAR CHEMISTRY AND PHYSICS · 2012 ·Vol. 213 ·期 20 ·2192-2200 · IF 2.361

pH-Responsive Double-Hydrophilic Block Copolymers: Synthesis and Drug Delivery Application

Xiao-Hui Dai,Chun-Yan Hong,Cai-Yuan Pan

A novel double-hydrophilic block copolymer P(MEO 2 MA- co -OEGMA)- b -PAMA has been successfully synthesized by two-step RAFT polymerization. Then, the amino groups of PAMA blocks in the copolymers react with 1-pyrenecarboxaldehyde via a “Schiff-base” reaction, and the resulting copolymers are self-assembled to form spherical micelles in aqueous solution. Because the “Schiff-base” linkage is pH sensitive, the release rate of pyrene depends upon the pH of solution. Complete release is achieved at pH 1, and the control release is much faster at pH 5.5 than that at pH 7.4. With progress of pyrene release, the micelles are disassembled gradually and disappeared completely at last. This double-hydrophilic copolymer is a promising candidate of drug carrier for the aldehyde- containing hydrophobic drugs.

研究领域: 高分子化学 · 药剂学 · 纳米医学 · 生物材料 · 药物递送系统
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 135 ·期 11 ·45974 · IF 1.86

Rheological and mechanical properties of thermoplastic polyurethane elastomer derived from CO2 copolymer diol

Wenqi Xian,Lina Song,Baohua Liu,Hulan Ding,Zhao Li,Mengping Cheng,Le Ma

CO 2 copolymer diol-based thermal polyurethane elastomers (PPC-TPU) were prepared by the reaction of CO 2 copolymer diol and methylene diphenyl diisocyanate and chain extender (ethylene glycol/1,4-butanediol/1,6-hexanediol) (EG/BDO/HG). The rheological and mechanical properties of PPC-TPU were analyzed. The effects of shear rate, shear temperature, hard segment content, and variety of chain extender on the properties of PPC-TPU were studied. The results showed that the apparent viscosity (η) of PPC-TPU decreased with the increasing shear rate ( τ ), and the non-Newtonian index ( n ) was less than 1. PPC-TPU exhibited a typical character of pseudoplastic non-Newtonian rheological behavior. The degradation during the processing was obviously inhibited by adding plasticizer and antioxidant. It was also discovered that the apparent viscosity varied with the content of hard segment and chain extender. Under the same temperature (185 °C) and shear rate (50 s −1 ), the apparent viscosity increased considerably with the raise of hard segment content, and the apparent viscosity and tensile strength of PPC-TPU with EG as chain extender was the maximum. It can be seen that with the apparent shear rate increasing, the variation tendency of apparent shear stress levels off, and the nonlinear relationship of τ – γ curve tended to be obvious. PPC-TPU exhibited a typical character of pseudoplastic non-Newtonian rheological behavior. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 45974.

研究领域: 高分子材料科学 · 流变学 · 功能高分子 · 生物基聚合物 · 材料力学
✓ 已验证 DOI 高影响因子
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JOURNAL OF APPLIED POLYMER SCIENCE · 2017 ·Vol. 134 ·期 29 ·45093 · IF 1.86

Influences of diallyl phthalate as chain extender on the properties of high molecular weight poly(vinyl chloride) resin

Jianning Wu,Baoxun Sui,Lei Li,Guihua Meng,Xuhong Guo,Zhiyong Liu

A higher porosity with better thermostability is desirable for poly(vinyl chloride) (PVC) resin. In this study, high molecular weight PVC resins are prepared by vinyl chloride monomer (VCM)-diallyl phthalate (DAP) suspension copolymerization in a 20-L reactor at 50 °C using DAP as chain extender. SEM, BET, and analyses of plasticizer absorption results show the high molecular weight poly(vinyl chloride) (HPVC) by DAP-VCM copolymerization is loose and porous. With increasing DAP content when the mass ratio of DAP/VCM (ω ) is below the gel point, the porosity and the degree of polymerization increase. Nevertheless, the bulk density and particle size decrease. When more than the gel point, these relationships are reversed. Thermogravimetric analysis revealed that the HPVC had better thermostability than that of commercial PVC, and its thermostability increases with increasing ω before it reaches the gel point. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 45093.

研究领域: 高分子化学 · 材料科学 · 聚合物合成 · 热分析 · 多孔材料
✓ 已验证 DOI 高影响因子
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