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971.
Peirui Zhang Fangqing Weng Ernest Koranteng Duyu Guo Pengfei Cao Qiangxian Wu 《应用聚合物科学杂志》2021,138(10):49963
Castor oil (CO) is an environmentally friendly renewable green resource and ideal alternative to petroleum resources. The preparation of high strength and high toughness castor oil-based polyurethane prepolymer (COPU) composites has significant applications such as supporting material and engineering plastic sheet. In this study, unmodified clam shell powder (CSP) with a unique CaCO3-proteoglycan structure was used as a filler to prepare compatible reinforced COPU composite materials. Investigation of the mechanical properties revealed that the elastic modulus of the composite COPU reinforced with 50 wt% of CSP had increased to 5859.0 ± 8.4 MPa representing 187.77% to obtain stiffer and stronger material over pure COPU (2036.6 ± 196.9 MPa). Moreover, the scanning electron microscopy, thermogravimetric analysis and contact angle results demonstrated that the reinforced COPU composites have better compatibility, thermal stability, and water resistance than pure COPU. This work will promote the application prospects of CO-based polyurethane. 相似文献
972.
Hailin Yu Yifan Xia Hanwen Zhang Xinjian Gong Pengfei Geng Zhenwei Gao Yinghan Wang 《应用聚合物科学杂志》2021,138(6):49803
In this work, semiinterpenetrating polymer network (semi-IPN), consisting of sulfonated poly (arylene ether sulfone) (SPAES) and crosslinked vinyl imidazole grafted polysulfone (VMPSU), is prepared and characterized. FTIR, EDS, and solubility test indicate the successful preparation of amphoteric membranes. The semi-IPN amphoteric membranes exhibit better stability than pure SPAES membrane, as demonstrated by thermogravimetric analysis and ex situ immersion testing results. More importantly, it is shown that the amphoteric membrane can effectively hinder vanadium ion crossover through the membrane, which is attributed to the semi-IPN structure and Donnan exclusion. As expected, the amphoteric membrane containing 20% VMPSU exhibits the highest proton selectivity (6.86 × 104 S min cm−3), comparing to pristine SPAES (1.90 × 104 S min cm−3) as well as Nafion117 (1.31 × 104 S min cm−3). 相似文献
973.
Component contacting degree in a composite material is an important reference for evaluation the performance characteristics. In this article, two composite material systems involving polylactic acid (PLA) with acrylonitrile butadiene styrene (ABS) and PLA with thermoplastic polyurethane (TPU) were prepared by blending and laminating through fused deposition modeling (FDM) 3D printing technology. The mechanical and thermal properties of the as-prepared composite materials were examined. The results indicated that PLA and TPU played a dominant role in tensile strength and breaking elongation, respectively, in individual composite material. ABS and TPU changed the glass transition peek, crystallinity, and modulus of PLA. The results also suggested that although the processing design of the blending method was more suitable for the contact between two components, but the mechanical properties of laminated composites were closer to theoretical predictions. The structural design and processing technology provide a comparative method and reference basis for studying the performance characteristics of composite materials. 相似文献
974.
Boqiong Xue Yuchun Li Jia Guo Jun Sun Xiaodong Liu Hongfei Li Xiaoyu Gu Sheng Zhang Shengling Jiang Zhiyuan Zhang 《应用聚合物科学杂志》2021,138(11):50015
In order to improve the flame retardancy and antistatic properties of polyamide 6 (PA6) at as low amount of additives as possible, an integrated-functional additive was synthesized by 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) and multiwalled carbon nanotubes (MWCNTs). The results showed 2 wt% of DOPO-MWCNTs distributed in PA6 formed an electric network and decreased volume resistivity sharply to 3.1 × 108 Ω cm. In other words, it helped PA6 to get to the percolation threshold of semiconductor. By using of 3 wt% DOPO-MWCNTs, the severe dripping in burning of PA6 was almost controlled. The possible reason was also ascribed to the network formed by evenly dispersed DOPO-MWCNTs, which strengthened the char structure and held severe dripping of PA6. As a result, the heat and smoke release were also suppressed obviously. The most important is that CO release was about half cut in CONE test. 相似文献
975.
Yun Liao Bing Cao Li Liu Xiandong Wu Sheng Guo Changhui Mi Kaiwen Li Meng Wang 《应用聚合物科学杂志》2021,138(15):50179
Two kinds of bio-based polyurethane coatings for controlled-release urea were prepared by in-situ polymerization used castor oil and liquefied starch as raw materials, respectively. Scanning electron microscopy (SEM) showed that the section morphology of castor oil based polyurethane (Castor-PU) coating was uniform and dense, and that of liquefied starch based polyurethane (Starch-PU) coating had certain proportion of microporous. Infrared spectroscopy (IR) showed that the two coatings had typical urethane characteristic structure, but the difference was that the Starch-PU had obvious unreacted isocyanate structure. Differential scanning calorimetry (DSC) showed that the glass transition temperature of the two coatings was around 58°C, but the Castor-PU had a crystallization domain with obvious crystallization melting peak at 130°C. Thermogravimetric analysis (TG) showed that the thermal stability of Castor-PU was significantly higher than that of Starch-PU. The controlled-release property test showed that when the coating ratio was 2.8%, the nutrient release longevity of urea coated with Castor-PU was 49 days and that of urea coated with Starch-PU was 14 days. The reasons for the poor controlled-release performance of Starch-PU were analyzed, which probably caused by concentrated sulfuric acid and hydrophilic dispersant added in the liquefied starch. 相似文献
976.
Owing to its high degree of crystallinity and orientation, the surface of aramid fiber is smooth, causing its low bonding strength with polymer matrix. This has restricted the application of aramid fiber in reinforced polymer materials. Effective methods are by introducing functional groups through surface modification and by increasing its surface roughness thereby greatly improving its bonding strength with the polymer. In this work, molecular dynamics (MD) simulation study fiber functionalized with hydroxyl (OH), carboxyl (COOH), and the silane coupling agent as nanofillers for polymer nanocomposites. The interfacial characteristics and the mechanical behavior of polymer nanocomposites are investigated. The results show that the functionalization can enhance the interfacial shear stress and tensile strength. The functional group not only provides a stronger interface, but also provides additional mechanical interlocking effect, which effectively improves load-bearing transmission capacity. The analysis of the micro-mechanism from the energy level also provides new insights for the functionalized design of nanocomposites. 相似文献
977.
Xing Yang Xianghua Wu Zhaoyang Chen Wenqiong Li Qi-Jun Sun Zeping Guo Xiaoguang Liang Yun He 《应用聚合物科学杂志》2021,138(20):50431
Coupling with electrospinning technique, metal–organic-frameworks (MOFs)-derived porous carbon fibers exhibit a great potential application in the adsorption of volatile organic compounds (VOCs) because of their huge surface area, high porosity, as well as sufficient heteroatom-doped active sites. In this work, the hierarchically porous N-doped carbon nanofibers are obtained after the pyrolysis of zeolite imidazole framework-8 and polyacrylonitrile (ZIF-8/PAN) composite fibers synthesized by electrospinning method. The N-doped carbon nanofibers fabricated in N2 atmosphere (N-CF-N2) present an enhanced adsorption capacity of 694 mg/g for benzene because of the synergistic effect of the hierarchically porous structure and the abundant N-species-containing active sites. It is also interesting that the N-doped hierarchical carbon nanofibers fabricated in Ar atmosphere (N-CF-Ar) exhibit a low benzene adsorption as compared with the N-CF-N2, which can be attributed to the porous structure damage caused by the bombardment of heavy Ar atoms on the pore shells during the pyrolysis. These results not only show a promising application of the as-fabricated N-CF-N2 in adsorption of VOCs for air purification due to its merit of cost-efficient, large-scale production, and excellent adsorption capacity, but also expand the potential of electrospinning technology and composite fibers in volatile organic gas adsorption. 相似文献
978.
Yan Song Kaifeng Chen Jingjing Wang Yuan Liu Jingzhi Yang Dawei Zhang Tao Qi Guo Liang Li 《应用聚合物科学杂志》2021,138(41):51214
It is highly desirable to develop self-healing anticorrosion coatings with enhanced antibacterial function to prevent the scratched area to be fouled or corroded in harsh environments. Herein, we report antibacterial self-healing anticorrosion coatings via the simple incorporation of the easily synthesized single polymer microcapsule system. Well-defined polymer microcapsules containing isophorone diisocyanate (IPDI) as a healing agent and 4,5-dichloro-2-n-octyl-4-isothiazolin-3-one (DCOIT) as antibacterial molecules were synthesized by one-pot polymerization. The diameter and core fraction were around 30 μm and 90%, respectively. The active DCOIT content in the core material could be precisely controlled by adjusting the DCOIT/IPDI feeding ratio. The DCOIT/IPDI microcapsules-embedded protective coating exhibits an adaptive self-healing anticorrosion property, as shown by electrochemical test under the condition of the salt-water immersion. Furthermore, the self-healing coating showed efficient antibacterial function against Escherichia coli and Pseudomonas aeruginosa, which is due to the released active biocide molecules on the damaged surfaces. In contrast to other systems, this single capsule system without any catalyst is perspective for extending the service time of the antibacterial self-healing materials in harsh environment. 相似文献
979.
Jing Lv Longhai Guo Chunjie Xie Weitong Xu Jun Ye Xiaoyu Li Teng Qiu Xinlin Tuo 《应用聚合物科学杂志》2021,138(44):51316
Being a new kind of nanomaterials, aromatic polyamide nanofibers (ANF) have been much highlighted in recent studies. We here demonstrate an isopropyl alcohol (IPA) accelerated chemical cleavage on poly (p-phenylene terephthalamide) chopped fibers, which provides an efficient preparation method of ANF. The comprehensive study on the processes accelerated by different alcohols revealed that the preparation time of ANF in the mixed medium of dimethyl sulfoxide (DMSO)-alcohol (20:1 in volume) was shorten to 45 min and 75 min for methanol (ethanol) and isopropanol, respectively. However, the nanofibers prepared in DMSO-IPA exhibited the minimum in axial and radial dimensions, providing the finest and most uniform diameter of 16 nm. The corresponding ANF films through vacuum assisted filtration also showed the highest tensile strength of 150 MPa, in comparison with those of the ANF films prepared using other alcohols, which were about 110 MPa. Furthermore, ANF/silicon hybrid films were prepared by the ionic ring-opening reaction followed by the alkoxysilane condensation and nanoparticle fabrication. By changing the organo functional groups in the alkoxysilane, the surface of the films were adjustable in a wide contact angle range from 56° (hydrophilic) to 150° (superhydrophobic), suggesting the amendable interfacial properties potential applicable to composite fabrication with most of the resin matrix. 相似文献
980.
针对电力系统暂态稳定评估中,电力系统同步相量测量装置(PMU)量测数据在采集和传输过程可能存在噪声问题,以及由于暂态稳定与失稳样本不平衡,导致基于数据驱动的暂态稳定评估模型训练的倾向性和误判后果严重问题,提出基于改进深度残差收缩网络(IDRSN)的电力系统暂态稳定评估方法.首先将底层量测电气量构建成特征图形式作为模型输入,利用模型深层结构建立输入与稳定结果之间的映射关系.面对噪声问题,模型通过注意力机制,采用软阈值函数自动学习噪声阈值,减小噪声及无关特征干扰;并通过焦点损失函数(FL),引入权重系数修正模型训练的倾向性,利用调制因子重点关注误分类样本,提高模型训练效率和评估性能.通过新英格兰10机39节点系统进行仿真分析,所提模型能够有效减小不同程度的噪声干扰,在不平衡数据集上修正模型训练偏向性,以减少误分类样本,在不同PMU配置方案下,均取得较好评估效果. 相似文献