JOURNAL OF APPLIED POLYMER SCIENCE
·
2018
·Vol. 136
·期 4
·47005
·
IF 1.901
C. Jiang,W. Liu,Y. Sun,C. Liu,M. Yang,Z. Wang
Superhydrophobic and superoleophilic cotton fabric was successfully prepared with fluorinated silica sol via a facile sol–gel method. A fluorinated polymeric sol–gel precursor (PHFBMA-MTS) was synthesized via free-radical polymerization by using hexafluorobutyl methacrylate (HFBMA) in the presence of (3-mercaptopropyl)trimethoxysilane (MTS) as the chain transfer agent, which led to the formation of fluoropolymer with alkoxysilane end groups. Then the fluorinated silica sol was prepared by introducing PHFBMA-MTS as the co-precursor of tetraethylorthosilicate (TEOS) in the sol–gel process with ammonium hydroxide as the catalyst, which was then used to fabricate superhydrophobic and superoleophilic fabric coatings through a simple dip-coating method. The coated fabrics showed superhydrophobic property with a high water contact angle of 154.1° and superoleophilic property with an oil contact angle of 0°. Moreover, the coated fabrics still kept superhydrophobicity even after ultrasonic treatment, as well as for organic solutions, acidic solutions. Thus, the coated fabrics were successfully applied to separate oil–water mixture with separation efficiency up to 99.8%. More importantly, the separation efficiency had no significant change after 20 cycles of oil–water separation. These present a simple, low-cost, and durable approach to achieve industrialized application of coated fabrics in oil–water separation. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136 , 47005.
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DOI
高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 138
·期 48
·51367
·
IF 3.125
Yujiao Gao,Dongning Liu,Yuanyuan Xie,Yiheng Song,Enwen Zhu,Zhuqun Shi,Quanling Yang,Chuanxi Xiong
In recent years, the wearable electronic skin (E-skin) has attracted more and more attention due to high sensitivity, good portability and flexibility. In this work, we used the 2,2,6,6-tetramethylpiperidinyl-1-oxyl (TEMPO)-oxidized cellulose nanofibril (TOCN) as the substrate, and used the in-situ polymerization method to introduce polypyrrole (PPy) into the TOCN substrate. Then, the nylon gauze was used as microstructure template to prepare a TOCN/PPy E-skin with a surface microstructure. This E-skin possessed excellent sensing and mechanical properties. In the pressure range of 0–600 Pa, the sensitivity of E-skin was 3.13 kPa −1 . In addition, the E-skin exhibited ultrafast response/recovery time (≤10 ms), ultralow detection limit of 0.3 Pa, good stability (>9000 cycles) and mechanical strength of up to 117 MPa. Therefore, the TOCN/PPy E-skin has broad development prospects in the fields of artificial intelligence and health monitoring.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 138
·期 34
·50853
·
IF 3.125
Junzhi Ma,Dong Wang,Shaohai Fu
To improve flame-retardant properties of unsaturated polyester resin (UPR), two phosphorus-containing vinyl monomers with different chemical structures were synthesized to replace styrene molecules and then copolymerized with UPR oligomers to prepare flame-retardant phosphatized UPRs. Curing behavior of phosphatized UPRs was investigated by DSC non-isothermal curing curves, deducing the best curing conditions. Cone calorimeter results demonstrated the obvious reduction of heat release rate and smoke production rate by comparing phosphatized UPRs with flammable UPR. TG-IR-MS coupling technique was utilized to reveal thermal degradation and pyrolytic volatiles including aromatic compounds, hydrocarbons, CO, PO 4 ˙, and so forth, providing more information of smoke toxicity and the gas phase flame- retardant mechanism of phosphatized UPRs. Moreover, the yield, compactness and graphitic degree of char residues of phosphatized UPRs were increased, strengthening the barrier effect to inhibit the permeation of combustion heat and the effusion of pyrolytic volatiles in the condensed phase.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 38
·e52918
·
IF 3.057
Yukun Tian,Yongzhi Hong,Yunlong Wang,Yuan Tian,Zhihao Wang,Meixing Ai,Jun Ma
The emerging stretchable and tough hydrogels find their extraordinary contributions in widespread use. However, the applicability of existing tough hydrogels in harsh environments like highly acidic stomachs has remained a challenge. Here, we develop superior stretchable and tough P(AA -co- AAm)/SiO 2 hybrid hydrogels through radiation-induced polymerization and crosslinking in the presence of acids. The performance of the nanocomposite gels was optimized by altering fabrication variables including acid concentration, monomer composition and absorbed dose. The mechanic tests show that the protonated hybrid hydrogels displayed a high elongation at break (1919%), fracture strength (117 kPa), and compressive strength at 50% strain (126 kPa). These values are superior to those of conventional polyelectrolyte hydrogels and expect to significantly broaden the application. The proposed strategy is quite general and offers an alternative strategy to develop tough hydrogels.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2023
·Vol. 140
·期 10
·e53601
·
IF 3
Zengwei Qin,Xiaohui He,Jiang Xu,Jiahao Deng,Xiujing Zang,Guoxiao Yang,Yao Lu,Shaoyu Zou,Liang Huang,Defu Chen
Solid polymer electrolytes (SPEs) have received extensive attention in the realm of lithium-ion batteries due to their safety performance, higher specific capacity and structural designability. In recent years, poly ionic liquids (PILs) have been attracting the attention of many researchers because of their high ionic conductivity, wide electrochemical stability window, high thermal stability and less-flammability in comparison with common liquid electrolytes. We selected imidazole cations as functional groups to be attached to the side chain of the polymer to prepare bis-imidazole functionalized benzo-norbornadiene monomer, which copolymerized with epoxy-functionalized norbornene monomer and norbornene (NB) monomer to obtain triblock copolymer. The prepared triblock copolymer was blended with lithium salt (LiTFSI) to obtain a solid polymer electrolyte membrane (SPEM). SPEM achieved an excellent ionic conductivity of 3.1 × 10 −5 S cm −1 at 30°C, exhibited an electrochemical stability window of up to 4.3 V versus Li/Li + (25°C) and thermal stability up to 275°C under protective (N 2 ) atmosphere. The NCM811/SPEM/Li batteries have exhibited a first discharging capacity of 149.1 mAh g −1 at 0.1 C-rate and the discharge capacity kept 141.6 mAh g −1 at 0.2 C-rate after 50 charge and discharge cycles at 30°C.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 46
·e53140
·
IF 3.057
Xuechen Zhuang,Shufen Zhang,Wei Ma
Composite films composed of biocompatible polymers are used widely in biomedical and food packaging areas. In this work, a new composite film with superior mechanical properties and biodegradability is prepared. The film is composed of biocompatible polyhydroxyethyl acrylate (PHEA) and starch, whose molecular chains are cross-linked using sucrose polyaldehyde (SPA), a green sucrose derivative. The composite film exhibits an optimal tensile strength and tensile strain of 11.5 MPa and 147.7%, respectively, which can be ascribed to the chemical cross-linking and hydrogen bond interactions between PHEA and starch. The tests confirm that the composite film shows satisfactory mechanical properties, hydrophilicity, and biodegradability, and thus should have wide applicability in biomedicine, food packaging, and other fields.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 138
·期 48
·51601
·
IF 3.125
Qianru Xu,Yaqi Zhang,Ruquan Zhang,Yongzhen Tao
Polyelectrolyte hydrogels with spinnability and electroresponsive were prepared from xanthan gum (XG) and gelatin. Oscillatory rheological measurements were utilized to explore mechanical properties and thermal stability of the resultant XG-Gelatin5 hydrogels. The XG-Gelatin5 hydrogels possessed higher strength and larger critical strain than these of the XG hydrogels, demonstrating existence of synergistic interactions. The XG-Gelatin5 hydrogels were stable in temperature range of 20–60°C, and gradually release drug with controlled manner in neutral and acid medium at 37°C. The self-recoverable and thixotropic XG-Gelatin5 hydrogels were extruded to form hydrogel fibers, and the dried hydrogel fibers rapidly bend towards cathode under applied voltage. Long hydrogel fibers were harvested with enhancement by Fe 3+ ions, and were weaved and braided to obtain hydrogel fiber constructs. The XG-Gelatin5 hydrogel fibers with electroresponsive and controlled drug release possess potential applications in biomaterials, tissue engineering, and drug carrier fields.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2024
·Vol. 141
·期 36
·e55915
·
IF 2.7
Tianyuan Liu,Weihao Wang,Tian Yin,Zhikui Jiang,Zhichao Zhen,Guochun Yan,Junhui Ji
The application and promotion of biodegradable plastics are hindered by the imbalance between their mechanical and degradation performance imbalance, as well as high costs. Herein, a series of poly(ethylene adipate-co-terephthalate) (PEAT) copolyesters with excellent mechanical and degradation properties are synthesized by one-step melt polycondensation. The influence of the proportion of aliphatic groups in the molecular chain on the structure and properties, especially the degradation performance, of the copolyesters was studied. The molecular chain flexibility and degradability of PEAT increases with increasing of adipic acid content and decreasing of ET fragment length ( L ET ). The comprehensive mechanical properties of PEAT60 can be comparable to traditional packaging material poly(butylene adipateco-terephthalate) (PBAT). The degradation performance of PEAT can be adjusted the molecular chain structure. PEAT with L ET < 3 exhibit degradation performance, and PEAT with L ET < 2.2 exhibit significant degradation acceleration. The excellent mechanical and degradable properties of PEAT copolyester make it expected to be used in degradable packaging and other fields to help solve plastic pollution, while its lower cost will aid in the promotion of degradable materials.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2020
·Vol. 138
·期 11
·49992
·
IF 2.52
Xiaoying Wang,Lili Wang,Bingyan Sun,Xiaomeng Chu,Xuteng Xing,Shaojie Liu,Erjun Tang
In this work, the sulfonated polystyrene brushes were grafted onto magnetic nanoparticles to obtain recoverable catalysts for efficient synthesis of ethyl N-phenylformimidate. First, the surface modification of Fe 3 O 4 with a particle size of about 10 nm was performed with the silane coupling agent of vinyl triethoxysilane (SG-151) to obtain Fe 3 O 4 with carbon–carbon double bonds on the surface (SG-Fe 3 O 4 ). Subsequently, SG-Fe 3 O 4 , styrene (St) and chloromethyl styrene (CMSt) were polymerized to obtain the magnetic chloromethylated polystyrene sphere (SG-Fe 3 O 4 @PS-Cl) with core-shell structure by solution copolymerization. Using St as monomer and SG-Fe 3 O 4 @PS-Cl as macromolecular initiator, the magnetic polystyrene brush of SG-Fe 3 O 4 @PS-PSt was obtained by activated regenerated electron transfer catalyst atom transfer radical polymerization. Finally, SG-Fe 3 O 4 @PS-PSt was sulfonated with sulfuric acid to form a magnetic sulfonated polystyrene brush of SG-Fe 3 O 4 @PS-PSH. SG-Fe 3 O 4 @PS-PSH was used as a recoverable acid catalyst to synthesize ethyl N-phenylformimidate. Due to the high loading of the sulfonic acid group of this catalyst, its added amount was lower than other solid acids such as p-toluenesulfonic acid. The results showed that the catalytic performance of SG-Fe 3 O 4 @PS-PSH was better than p-toluenesulfonic acid and commercial macroporous sulfonic acid resin. The external magnetic field can directly recover SG-Fe 3 O 4 @PS-PSH, simplifying the recovery of catalyst and reducing the catalyst loss. After recycling, the yield of ethyl N-phenylformimidate was not significantly decreased.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2020
·Vol. 138
·期 9
·49913
·
IF 2.52
Mengwei Dai,Pan Song,Yong Zhang
A castor oil (CO) was modified via thiol-ene click chemistry reaction between CO and 3-mercaptopropyl trimethoxysilane, with the conversion of CC bonds of CO over 99% based on 1 HNMR spectra. The obtained modified castor oil (MCO) was used as a biobased polyol to prepare waterborne polyurethane (WPU) dispersions. The modification of CO exhibited a great effect on the properties of WPU dispersions and coatings, and an obvious change is the improvement of the water resistance of WPU coatings. WPU dispersions with MCO had good storage stability. A WPU coating with 7% MCO had high surface hydrophobicity, and its water absorption was as low as 3.2%. Conductive carbon black filled WPU coatings with MCO were cured by efficient UV radiation, and their conductive percolation threshold could decrease to 0.76%, which could be attributed to the well filler dispersion and strong filler-polymer interaction. The WPU dispersions are ecofriendly, and can be used to produce biobased WPU coatings with a great application potential in antistatic coating fields.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2021
·Vol. 139
·期 18
·52059
·
IF 3.125
Xi Hou,Liwen Sun,Wei Wei,Darlene K. Taylor,Shengpei Su,Haibin Yu
Thermoplastic polyurethane (TPU) has become the focus of attention in the green and sustainable materials field because of its superior processability and recyclability. In this paper, a series of polylactic acid (PLA) and polycaprolactone (PCL)-based TPUs were successfully prepared by selecting PLA glycol, PCL glycol, isophorone diisocyanate (IPDI) and 1,4-butanediol (BDO) through a one-step polymerization method. The properties of the PLA and PCL-based TPUs are comprehensively characterized by Fourier transform infrared spectroscopy, 1 H NMR spectra, gel permeation chromatography, differential scanning calorimetry, thermalgravimetric analyzer, tensile test, dynamic mechanical analysis, scanning electron microscope, and so forth. The effect of hard segments content and PLA glycol molecular weight on the properties of PLA and PCL-based TPUs was systematically studied. Notably, their performance shows a certain degree of regularity and can be controlled by adjusting the hard segments content or the molecular weight of the PLA glycol. The prepared PLA and PCL-based TPUs have a tensile strength of 24.71 MPa, excellent thermal stability and out-standing damping performance. Its tan δ max of 1.40 and an effective damping temperature range of 50°C also make it a green damping material with great potential.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2015
·Vol. 133
·期 16
·
IF 1.768
Zhiyong Lv,Chonggang Wu,Jing Li,Xiao Fang,Dongdong Yu,Huchuan Qin,Peng Yu,Xuhuang Chen
A new high-ultraviolet (UV)-transmission silicone-resin polymeric material was prepared via curing during hydrosilylation of tetramethyltetravinylcyclotetrasiloxane with tetramethylcyclotetrasiloxane by a liquid-surface supernatant method, using a stepwise heating program to avoid spontaneous combustion of the reaction mixture. The relationships were investigated in detail between reactive groups, cross-linking density, mechanical and UV-transmission properties. For this purpose, UV transmittance and dynamic mechanical properties, respectively, of the silicone resin were measured with UV–visible spectrophotometry and dynamic mechanical thermal analysis. In addition, surface roughness was evaluated with an atomic force microscope as well as an interferometer. The curing process was monitored by Fourier transform infrared spectroscopy and rotational rheometry. The cyclic silicone oils were compared with linear ones in structure and product properties. The results indicated that stepwise temperature control during curing process was particularly indispensible due to the presence of active Si H bonds, and that the silicone resin of high modulus, high UV transmittance (92.7%) and low surface-roughness was largely homogeneous in cross-linking points distribution. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133 , 43308.
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DOI
高影响因子
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