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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 6 ·48358 · IF 2.188

Synthesis of pH-responsive isolated soy protein/carboxymethyl chitosan microspheres for sustained pesticide release

Long Chen,Xinhua Zhou,Guanquan Lin,Huayao Chen,Li Hao,Hongjun Zhou

In order to improve the utilization rate of avermectin (AVM), a complex was prepared by electrostatic self-assembly using isolated soy protein (ISP) and carboxymethyl chitosan (CMCS) for loading AVM to obtain ISP/CMCS@AVM microspheres. The encapsulation efficiency (EE), sustained release property, ultraviolet (UV) protective ability, and toxicity of the microspheres were evaluated, and the release kinetics of AVM from the microsphere at different pHs were investigated. The results demonstrated that the average particle size of ISP/CMCS@AVM was 283.95 nm, and the EE reached 88.42% for AVM after denaturation. After 70 h of exposure to UV light, the residual rate of AVM in ISP/CMCS@AVM was 78.12%, which was significantly higher than 35.18% in the AVM emulsion. Moreover, the formulation imparted pH sensitivity and sustained-release property to AVM and was consistent with the Korsmeyer–Peppas model, controlled by Fick diffusion. Finally, the insecticidal toxicity of ISP/CMCS@AVM did not differ significantly from that of unmodified AVM. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 48358.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2015 ·Vol. 133 ·期 16 · IF 1.768

Stepwise cure and properties of silicone resin for high-ultraviolet-transmission optical elements

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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JOURNAL OF APPLIED POLYMER SCIENCE · 2020 ·Vol. 138 ·期 11 ·49992 · IF 2.52

Sulfonated polystyrene brushes grafted onto magnetic nanoparticles as recoverable catalysts for efficient synthesis of ethyl N-phenylformimidate

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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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 32 ·50790 · IF 3.125

Synthesis of reactive self-adhesive branched polyurethane dispersant for textile pigment printing

Tengchao Zeng,Guiping He,Xinxiang Li,Chaoxia Wang

A series of reactive branched polyurethane dispersants (BPUs) were successfully synthesized based on epoxy as reactive group and nitrogen-containing heterocycles as anchoring group. The branched polyurethane was adopted an ''A 2 + B 3 '' approach with diisocyanate prepolymer and trimethylolpropane. The structure, molecular weight, and thermodynamic property of BPUs were characterized. The pigment dispersions were prepared with BPUs as the dispersant by ball milling, and then the characteristic parameters such as pigment particle size, viscosity, stability, color properties, and fastness were evaluated. Excellent dispersing performances were observed that the particle size of five dispersions were below 200 nm, with the viscosity as low as 6–9 mPa·s. It is worth noting that the pigment dispersion prepared by BPU exhibited excellent stability and self-adhesive performance. These dispersions were printed on cotton fabrics without adhesives, their water washing fastness was approximately grade 4. And the dry rubbing and wet rubbing fastnesses were 3 and 2–3, respectively.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2022 ·Vol. 139 ·期 32 ·e52774 · IF 3.057

Artificial neural network prediction of thermal and mechanical properties for Bi2O3-polybenzoxazine nanocomposites

Mohamadou Al Hassan,Mehdi Derradji,Mohsen M. M. Ali,Abdullah Rawashdeh,Jun Wang,Zhong-Cheng Pan,Wen-Bin Liu

Polybenzoxazine (BA-a) based nanocomposites with varying amounts of Bi 2 O 3 particles reinforcement (10, 20, and 30 wt%) were produced. The structures of the Bi 2 O 3 before and after surface silane treatment, as well as the structures of the BA-a matrix and its nanocomposites, were all evaluated using Fourier transform infrared spectroscopy (FTIR). The thermal stability of the samples was evaluated by thermogravimetric analysis (TGA) and the resistance to bending was studied using the three-point bending test. Then, an artificial neural network approach was used to estimate the thermal degradation and flexural strengths of the polybenzoxazine matrix and its nanocomposites. The results of the TGA analysis showed that when Bi 2 O 3 content increased, the char yield ( Y c ) of the nanocomposites also increased from 27.98% to 43.53% for the experimental data and from 27.95% to 43 0.57% for the prediction, with all SD s less than 0.02. Moreover, both the experimental and predicted values of the flexural strengths for the unfilled BA-a displayed 100.40 and 102.96 MPa, respectively and these values increased to 119.65 and 114.95 MPa when 10 wt% of fillers were incorporated into the matrix. However, for higher filler contents, 20 and 30 wt%, these values decreased to 112.94 and 108.01 MPa for the experiments, and 106.35 and 103.20 MPa for the prediction, respectively. The very small deviations (<0.05) between the experimental and predicted values demonstrated that the prediction approach using the artificial neural network is reliable and accurate.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 15 ·48558 · IF 2.188

Influences of (3-aminopropyl)triethoxysilane on the tribological behaviors of basalt fiber/acrylonitrile-butadiene rubber composites under dry friction and water-lubricated conditions

Yingzhe Li,Zhuo Li,Yang Gao,Lin Li,Yihan Yang

The weak interaction between the basalt fiber (BF) and acrylonitrile-butadiene rubber (NBR) weakens the BFs' effects on improving the tribological performances of the NBR composites. To solve this problem, (3-aminopropyl)triethoxysilane (APTES) was introduced via mixing into the matrix or grafting on the BF surface, respectively. The characteristics, mechanical, and tribological properties of the composites were evaluated, and the effects of the APTES and its introduction methods on the tribological properties were the main focus. The APTES mixed in the rubber matrix decreased the friction coefficient (COF) of the NBR-based composites under both dry friction and water-lubricated conditions. Especially, the APTES hydrolysis under water-lubricated condition was conducive to the formation of the water film and thus dramatically decreased the COF. The COF of the BF0-A3 and the BF12-A3 were 51% and 30% lower than that of the BF0-A0 and the BF12-A0 under water lubrication, respectively. The APTES grafted on the BF surface increased the wear resistance of the BF/NBR composites attributed to the improvement of the interaction between the BFs and the NBR matrix. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 48558.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2016 ·Vol. 134 ·期 9 · IF 1.866

Small-molecule-induced miscibility of isosorbide-based polycarbonate with bisphenol A polycarbonate

Lili Su,Wenqin Lai,Jin Yan,Guozhang Wu

In this study, we investigated the influence of the small molecule 4,4′-thiobis(6- tert -butyl- m -methyl phenol) (AO300) on the miscibility of poly(isosorbide- co -1,4-cyclohexanedimethanol carbonate) (I c C–PC) with bisphenol A polycarbonate (BPA–PC) through the formation of hydrogen-bonding networks. Differential scanning calorimetry and morphological observation revealed that the initially, immiscible BPA–PC/I c C–PC blends become miscible through the addition of small molecules. Fourier transform infrared spectroscopy confirmed that intermolecular hydrogen bonds formed between the hydroxyl groups of AO300 and the carbonyl groups of the studied polycarbonates. These polycarbonates exhibited different hydrogen-bonding behaviors and various degrees of glass-transition temperature composition dependence. Dynamic mechanical analysis demonstrated that AO300 played an antiplasticization role in the BPA–PC/I c C–PC blends with improved storage moduli. To our knowledge, this article is the first to describe the miscibility of isosorbide-based polycarbonate with BPA–PC. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44537.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2018 ·Vol. 135 ·期 23 ·4634159 · IF 1.901

Facile preparation and characterization of soluble aramid

Sheng Zhou,Xiaolu Wang,Wei Zhang,Mengyao Zhang,Xiaoli Zhang,Ning Zhao,Ruigang Liu,Jian Xu,Zhihao Shen,Xinghe Fan

It remains a problem to prepare cost-effective aramid with good solubility via a simple method since the commercialization of aromatic polyamides such as Kevlar and Nomex by DuPont in 1960s. Herein, we report the facile preparation and properties of an aromatic polyamide copolymerized by 2,6-naphthalene dichloride (26N-COCl), 4,4′-oxydianiline, and m -phenylenediamine. The synthetic route is very facile and cost-effective. The modified aramids possess excellent comprehensive properties. The polymers are soluble in some organics. Their thermal stabilities are excellent, with 5% weight loss temperatures ( T d ,5% 's) in air higher than 460 °C and glass transition temperatures ( T g 's) higher than 280 °C. These polymers are easily processed into films, fibers, and tubes. The products exhibit high strength. For example, the films have excellent mechanical strength, with a tensile strength up to 139 MPa, a tensile modulus up to 3.45 GPa, and an elongation of 11%. The films are also transparent and fluorescent. The overall properties are better than those of the commercial Nomex. The facilely prepared aramids with good solubility are very promising for commercial use. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135 , 46341.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 139 ·期 4 ·51548 · IF 3.125

Effects of networks composed of epoxy/dual thiol-curing agents on properties of shape memory polymers

Yanling Wang,Longhao Tang,Yongfei Li,Qiang Li

Profound understanding of relationships between molecular networks with properties can make it more convenient for people to prepare and employ shape memory polymers (SMPs). In this paper, a series of epoxy SMPs were developed based on epoxy (E-51), trimethylolpropane tris(3-mercaptopropionate) and pentaerythritoltetrakis (3-mercaptopropionate), and 2-methylimidazole, through “epoxy-thiol” click reaction. The effect of networks on key properties (heat resistance and mechanical properties shape recovery performance) was systematically investigated. Experiment results indicated that there were positive correlations between network regularity with both thermal–mechanical properties and heat resistance. In addition, regularity of network structure had an effect to restrict shape recovery speed.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 139 ·期 1 ·51440 · IF 3.125

Construction of waste-collagen modified superfine fiber substrates based on “click” chemistry: Moisture absorption and permeability

Na Xu,Yanmei Xing,Xuechuan Wang,Longfang Ren,Taotao Qiang

Superfine fiber synthetic leather is a high-grade artificial leather product with numerous characteristics and advantages. However, compared with natural leather, it shows poor moisture absorption and moisture permeability, and it gives people a hot and tacky feeling; thus, the improvement of these properties has become a popular topic in the industry. In this paper, the “click” chemistry method was employed to modify the nylon fiber of the superfine fiber synthetic leather base with waste collagen to improve the moisture absorption and permeability of the superfine fiber synthetic leather base, thus enhancing the hygienic performance and wearing comfort of the end products, realizing waste recycling. This study obtained the optimal reaction conditions for the “click” modification of unfigured sea-island superfine fiber synthetic leather base with collagen methacrylamide. The characterizations by static contact angle measurements, attenuated total reflection infrared spectroscopy, and X-ray photoelectron spectroscopy analysis confirmed that collagen was successfully grafted onto the surface of the nylon fiber. Compared with the original base, the moisture absorption, and permeability of the base were improved by 602.4% and 43%, respectively. This study shows the theoretical research significance and excellent practical value for the resource utilization of skin collagen waste.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2018 ·Vol. 137 ·期 2 ·47298 · IF 1.901

Enhancement of flame retardancy and mechanical properties of polyamide 6 by incorporating melamine cyanurate combined with attapulgite

Wei Hou,Yifan Fu,Cen Zeng,Na Liu,Cuiyu Yin

In this study, the nanocomposites are prepared which used polyamide 6 (PA6) composite as matrix, melamine cyanurate (MCA) as fire retardant and attapulgite (AT) as synergistic agent. The mathematical model between MCA content, AT content, and limited oxygen index (LOI) is established by multiple linear regression fitting. The polymer materials are characterized using Fourier transform infrared spectroscopy, X-ray diffraction, Thermogravimetric Analysis, and scanning electron microscopy. Through response surface methodology, the important variables (polymerization time, the content of MCA, and the content of AT) affecting the mechanical strength of composites are modeled. Results demonstrate that when the t is 0.6 h, the AT content is 6.2%, and the MCA content is 11.5%, the mechanical properties of the PA6/MCA/AT composite are up to 44.81 MPa, and the sample passes the UL-94 V-0 flammability rating, and the LOI reaches 27.9%. Therefore, polymers with highly effective flame retardancy and optimal mechanical properties are prepared. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 47298.

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JOURNAL OF APPLIED POLYMER SCIENCE · 2021 ·Vol. 138 ·期 29 ·50685 · IF 3.125

Enhancement of dynamic mechanical properties and flame resistance of nanocomposites based on epoxy and nanosilica modified with KR-12 coupling agent

Ngoc Minh Ho,Thuy Chinh Nguyen,Thi Thanh Van Tran,Tien Dung Nguyen,Hoang Thai

The epoxy/silica nanocomposites containing a wide range of isopropyltri[di(octyl) phosphate] titanate coupling agent (KR-12) modified nanosilica (m-nanosilica) loading (0–7 wt%) cured with tetrabutyl titanate hardener were prepared. Their morphology, thermal stability, thermal expansion, and mechanical properties including hardness, abrasion resistance were investigated. The wetting ability of epoxy-nanosilica systems on glass surface was assessed based on static contact angle. The obtained results showed that the contact angle of the nanocomposites containing m-nanosilica is slightly changed as compared to the contact angle of pure epoxy resin and lower than that of the nanocomposite containing unmodified nanosilica. The data of dynamic mechanical analysis of the nanocomposites using different nanosilica content indicated that the presence of m-nanosilica lowered the recovery energy of the nanocomposites to 41.62% as compared to neat epoxy. The limiting oxygen index (LOI) of the nanocomposites confirmed that the m-nanosilica increased the flame retardance of epoxy matrix. When using 7 wt% of m-nanosilca, the LOI value of the nanocomposite was 27.4 while this index of neat epoxy was 21.6. The scanning electron microscopic images of residual char combustion of the nanocompsites indicated a formation of nanosilica layer contributed to restrain combustion of the material.

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