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Preparation of Monomer Casting Nylon-6-b-Polydimethylsiloxane Copolymers with Enhanced Mechanical and Surface Properties 提高机械性能和表面性能的单体铸造尼龙-6-b聚二甲基硅氧烷共聚物的制备
Q2 Materials Science Pub Date : 2018-11-02 DOI: 10.1080/03602559.2017.1410846
Jie Ying, Wenqi Wang, Xing Peng, Zhoutong Qiu, Xiang Ma, Sai Zhang, Jikui Wang
ABSTRACT Nylon-6-b-polydimethylsiloxane copolymer was synthesized with macroinitiator through in situ polymerization. The macroinitiator with two chain-growing centers per molecule is based on hydroxyl terminated polydimethylsiloxane (PDMS) functionalized with diisocyanate. The influence of PDMS contents on the properties of copolymers was studied. Differential scanning calorimetry and X-ray diffraction were used to investigate the melting temperature, crystallization temperature and crystal form of samples, and the results showed that the crystallinity of polymers decreased. The mechanical properties of samples were studied by notched-impact testing and tension test. The notched impact strength was improved by 200% with PDMS concentration up to 4 wt%. The form of scaly was seen by scanning electron microscope proved the improvements of the impact strength of the copolymer. The water contact angles test showed that the surface tension of copolymers decreased with the PDMS content increasing and the surface of copolymer changed from hydrophilic to hydrophobic. GRAPHICAL ABSTRACT
摘要采用原位聚合的方法,用高分子引发剂合成了尼龙-6-b聚二甲基硅氧烷共聚物。该高分子引发剂以端羟基聚二甲基硅氧烷(PDMS)为基料,二异氰酸酯功能化,每个分子具有两个链生长中心。研究了PDMS含量对共聚物性能的影响。采用差示扫描量热法和x射线衍射法研究了样品的熔融温度、结晶温度和结晶形态,结果表明聚合物的结晶度下降。通过缺口冲击试验和拉伸试验研究了试样的力学性能。当PDMS浓度达到4 wt%时,缺口冲击强度提高200%。扫描电镜观察到鳞片的形成,证明了共聚物抗冲击强度的提高。水接触角测试表明,随着PDMS含量的增加,共聚物的表面张力降低,共聚物表面由亲水性变为疏水性。图形抽象
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引用次数: 11
Exploring the Influence of Methylene Diphenyl Diisocyanate as a Modifier for Ethylene Vinyl Acetate/Thermoplastic Polyurethane Blends 探讨亚甲基二苯基二异氰酸酯作为改性剂对醋酸乙烯/热塑性聚氨酯共混物的影响
Q2 Materials Science Pub Date : 2018-11-02 DOI: 10.1080/03602559.2017.1410847
Joy Dutta, Tuhin Chatterjee, Padmanabhan Ramachandran, K. Naskar
ABSTRACT Ethylene vinyl acetate (EVA)/thermoplastic polyurethane (TPU) blend at various blend ratios has been modified via reactive processing with 4,4′-methylene diphenyl diisocyanate (MDI). Modification of the blends with even small amount of MDI shows significant improvement in physico-mechanical properties for EVA/TPU 50/50 and 30/70 blends, and it is also supported by the superior melt rheological behavior and dramatic improvement in oil resistance property. After the treatment of electron beam (dose range: 50–150 kGy), radiation crosslinked EVA/TPU (30:70) blend reveals further improvement in various properties. This particular material can find potential application as cable sheathing component. GRAPHICAL ABSTRACT
摘要采用4,4′-亚甲基二苯基二异氰酸酯(MDI)对不同配比的乙烯乙酸乙烯酯(EVA)/热塑性聚氨酯(TPU)共混物进行反应改性。即使加入少量MDI,也能显著改善EVA/TPU 50/50和30/70共混物的物理力学性能,并得到优异的熔体流变性能和耐油性能的显著改善。经电子束(剂量范围:50 - 150kgy)处理后,辐射交联EVA/TPU(30:70)共混物各项性能进一步改善。这种特殊的材料可以找到潜在的应用作为电缆的护套组件。图形抽象
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引用次数: 5
Examination of Interpenetrating Polymer Networks of Polyurea in Silicone Molds Arising during Vacuum Casting Processes 真空铸造过程中聚脲在硅胶模具中互穿聚合物网络的研究
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1410838
Martin Wortmann, N. Frese, Alexander L. Heide, Johannes Brikmann, Oliver I. Strube, Raphael Dalpke, A. Gölzhäuser, E. Moritzer, Bruno Hüsgen
ABSTRACT We present an in-depth investigation of the aging effects in silicone molds for vacuum casting processes. Their lifetime is limited to a few production cycles due to contamination with the diisocyanate component of polyurethane casting materials. Using thermogravimetric analysis measurements, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and helium-ion-microscopy the chemical and physical mechanisms of the aging process have been identified. It has been shown that a diffusion process of diisocyanate into the cavity surface leads to the formation of interpenetrating polymer networks of polyurea derivatives in silicone rubber. This has been proven by extracting and analyzing polyurea of low molecular weights from the silicone. GRAPHICAL ABSTRACT
摘要:我们对真空铸造过程中硅树脂模具的时效效应进行了深入的研究。由于聚氨酯铸造材料的二异氰酸酯成分的污染,它们的使用寿命仅限于几个生产周期。利用热重分析测量、傅里叶变换红外光谱、x射线光电子能谱和氦离子显微镜,确定了老化过程的化学和物理机制。研究表明,二异氰酸酯在硅橡胶中的扩散过程导致聚脲衍生物的互穿聚合物网络的形成。通过从硅胶中提取和分析低分子量聚脲,证明了这一点。图形抽象
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引用次数: 6
Effect of Lithium Perchlorate on the Optoelectrical and Thermal Properties of Poly(Vinylpyrrolidone)/Nano-Cesium Aluminate Solid Polymer Electrolytes 高氯酸锂对聚(乙烯基吡咯烷酮)/纳米铝酸铯固体聚合物电解质光电和热学性能的影响
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1410841
Adel Saeed, M. Al-Gunaid, Siddaramaiah
ABSTRACT Solid polymer electrolyte (SPE) of polyvinylpyrrolidone (PVP) with varying amounts, namely, 5, 10, and 15 wt% of lithium perchlorate (LiClO4) as an electrolyte and 8 wt% cesium aluminum oxide (CsAlO2) nanoparticle have been fabricated by solution intercalation technique. The optoelectrical behaviors of the SPE films have been evaluated using UV–visible spectroscopy. The UV–visible spectral studies revealed the UV light-absorbing nature of NC films with considerable visible transparency. The chemical structure and morphological behaviors of PVP/8 wt% of CsAlO2–LiClO4 SPE films have been established by Fourier transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy, respectively. The AC conductivity of the SPEs was evaluated at room temperature by digital LCR meter in the frequency range 100 Hz–5 MHz. The thermal behaviors such as Tg and degradation patterns of the SPEs have been evaluated using differential scanning calorimetric analysis and thermogravimetric analysis, respectively. GRAPHICAL ABSTRACT
采用溶液插层技术制备了聚乙烯吡咯烷酮(PVP)固体聚合物电解质(SPE),电解质分别为5、10、15 wt%的高氯酸锂(LiClO4)和8 wt%的氧化铈(CsAlO2)纳米颗粒。利用紫外可见光谱法对SPE薄膜的光电性能进行了评价。紫外-可见光谱研究揭示了NC膜的紫外吸收特性,并具有相当的可见光透明度。利用傅里叶变换红外光谱、x射线衍射和扫描电镜分别对PVP/ 8wt % CsAlO2-LiClO4 SPE膜的化学结构和形态行为进行了表征。在100hz - 5mhz的频率范围内,用数字LCR计测量了室温下spe的交流电导率。用差示扫描量热分析和热重分析分别评价了SPEs的热行为,如Tg和降解模式。图形抽象
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引用次数: 9
Correlation Between Crystallization Behavior and Mechanical Properties of Biodegradable Poly(Caprolactone-co-Cyclohexene Carbonate) 可生物降解聚己内酯-共环己烯碳酸酯结晶行为与力学性能的关系
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1410839
Limiao Lin, Yonghang Xu, Jiaxiang Qin, Shuanjin Wang, M. Xiao, Y. Meng
ABSTRACT The isothermal and nonisothermal crystallization behaviors of poly(ε-caprolactone) and poly(caprolactone-co-cyclohexene carbonate) were investigated utilizing differential scanning calorimeter and polarized optical microscope. The kinetic of isothermal crystallization could be well defined by Avrami equation, while Mo model was successful to describe the nonisothermal crystallization. Based on the obtained kinetic parameters, poly(cyclohexene carbonate) segments not only act as a nucleating agent accelerating nucleating rate but also restrict the transport of poly(ε-caprolactone) segments decelerating growth rate. The mechanical properties of polymers were investigated using DMA and nanoindentation. It shows that the insertion of hard poly(cyclohexene carbonate) segments improves Young’s modulus and heat resistance but reduces hardness of copolymers. GRAPHICAL ABSTRACT
利用差示扫描量热仪和偏光显微镜研究了聚(ε-己内酯)和聚(己内酯-碳酸共环己烯)的等温和非等温结晶行为。Avrami方程可以很好地定义等温结晶的动力学,而Mo模型可以很好地描述非等温结晶。根据得到的动力学参数,聚碳酸环己烯段不仅作为成核剂加速成核速率,而且还限制聚ε-己内酯段的输运,减缓了聚ε-己内酯段的生长速率。利用DMA和纳米压痕技术研究了聚合物的力学性能。结果表明,硬聚碳酸环己烯段的加入提高了共聚物的杨氏模量和耐热性,但降低了共聚物的硬度。图形抽象
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引用次数: 6
Erratum to “Novel Facial Conducting Polyamide-Based Dithiophenylidene Cyclyhexanone Moiety Utilized for Selective Cu2+ Sensing” “基于聚酰胺的新型面部导电二噻吩基环己酮片段用于选择性Cu2+传感”的勘误
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1409936
M. Hussein, M. M. Rahman, Abdullah M. Asiri
ABSTRACT The present work is aimed to synthesize a novel series of linear polyamides (PAs) 4a–d based on di(thiazolyl-thiophenylidene)cyclyhexanone as well as carries aliphatic and aromatic species in the polymer main backbones. The polymerization process was occurred by solution polycondensation technique by the interaction of the newly synthesized monomer 3 with adepoyl, sebacoyl, terphthaloyl, and isophthaloyldiacid chlorides. Before polymerization, the structure of monomer 3 was confirmed by elemental and spectral analyses. The structures of polymers were also investigated by elemental, spectral analysis, thermal analysis, and Field-Emission Scanning Electron Microscopy (FE-SEM) micrographs. Film draw temperatures for all the polymers were evaluated in the range 509.0–542.3°C. Here, the heavy metallic sensors are developed with the polyamide-fabricated glassy carbon electrode (GCE) by reliable current vs. voltage technique. A thin layer of PA onto GCE was fabricated with conducting coating agents (5% nafion) to fabricate a selective heavy metal ions, Cu2+ sensor in short response time in phosphate buffer phase. The fabricated sensor was also exhibited higher sensitivity, lower detection limit, large dynamic concentration ranges, long-term stability, and improved electrochemical performances toward Cu2+ sensor. The calibration plot is linear (r2: 0.9956) over the large Cu2+ ion concentration ranges (1.0 nM to 10.0 mM). The sensitivity and detection limit is 3.4177 µA cm−2 µM−1 and 0.36 nM (signal-to-noise ratio of 3) respectively. This novel effort is initiated a well-organized way of efficient cationic sensor improvement with conductive polymers for heavy metallic pollutants in environmental and health-care fields in large scales. GRAPHICAL ABSTRACT
摘要本研究以二(噻唑基-噻吩基)环己酮为主要骨架,以脂肪族和芳香族为主要骨架,合成了一系列新的直线型聚酰胺(PAs) 4a-d。通过溶液缩聚技术,将新合成的单体3与二甲酰、癸二酰、三苯二酰和异苯二酰氯相互作用,进行了聚合反应。聚合前对单体3的结构进行了元素分析和光谱分析。通过元素分析、光谱分析、热分析和场发射扫描电子显微镜(FE-SEM)对聚合物的结构进行了研究。所有聚合物的薄膜拉伸温度在509.0-542.3°C范围内进行评估。本文采用可靠的电流vs电压技术,利用聚酰胺制造的玻碳电极(GCE)开发了重金属传感器。采用导电涂层剂(5% nafion)在GCE表面制备了一层薄层PA,在磷酸盐缓冲相中快速响应制备了选择性重金属离子Cu2+传感器。该传感器对Cu2+具有较高的灵敏度、较低的检出限、较大的动态浓度范围、长期的稳定性和较好的电化学性能。在较大的Cu2+浓度范围内(1.0 nM ~ 10.0 mM),校正图呈线性关系(r2: 0.9956)。灵敏度为3.4177µA cm−2µM−1,检出限为0.36 nM(信噪比为3)。这种新颖的努力是在环境和卫生保健领域大规模利用导电聚合物对重金属污染物进行高效阳离子传感器改进的一种组织良好的方式。图形抽象
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引用次数: 5
Compatibilizer Assistant SCF/ABS Composites with Improved Mechanical Properties Prepared by Fused Deposition Modeling 熔融沉积法制备具有增强力学性能的增容助剂SCF/ABS复合材料
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1410843
Jinchun Zhu, Jian Zhang, Jindao Wang, Biao Wang
ABSTRACT A random terpolymer copolymer of styrene, acrylonitrile and glycidyl methacrylate (SAG) was used as compatibilizer to improve the interfacial adhesion of short carbon fiber (SCF)/acrylonitrile-butadiene-styrene (ABS) composites. Effects of SAG on the structural and mechanical properties of fused deposition modeling (FDM) printed composites were investigated. The results showed the addition of SAG could effectively improve the interfacial adhesion between SCF and ABS matrix, whereas slightly decrease average length of SCF and degrade the adhesion quality among deposited filaments. As a result, the tensile and flexural properties of FDM printed composites initially increased and then decreased with the SAG content. GRAPHICAL ABSTRACT
摘要:采用苯乙烯、丙烯腈和甲基丙烯酸缩水甘油酯(SAG)三元共聚物作为增容剂,提高短碳纤维(SCF)/丙烯腈-丁二烯-苯乙烯(ABS)复合材料的界面附着力。研究了表面活性剂对熔融沉积建模(FDM)打印复合材料结构和力学性能的影响。结果表明,SAG的加入能有效改善SCF与ABS基体之间的界面粘附,但会略微降低SCF的平均长度,降低沉积细丝之间的粘附质量。结果表明,随着SAG含量的增加,FDM打印复合材料的拉伸和弯曲性能呈现先上升后下降的趋势。图形抽象
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引用次数: 8
Delamination of Mg-Al Layered Double Hydroxide on Starch: Change in Structural and Thermal Properties 镁铝层状氢氧化物在淀粉上的分层:结构和热性能的变化
Q2 Materials Science Pub Date : 2018-10-13 DOI: 10.1080/03602559.2017.1410844
S. Swain, S. Barik, G. C. Pradhan, L. Behera
ABSTRACT Mg-Al layered double hydroxide decorated starch bionanocomposites (starch/layered double hydroxide) are prepared by solution intercalation method. The bionanocomposites are systematically characterized by Fourier transform infrared spectroscopy, X-ray diffraction, and high-resolution transmission electron microscopy techniques. The thermal stability of starch is enhanced due to dispersion of layered double hydroxide within the starch matrix. The chemical resistance property of starch is improved substantially with slight sacrifice in biodegradation behavior by the delamination of layered double hydroxide in starch matrix. Herein, layered double hydroxide acts as potential laminated filler for change in structural, thermal, and chemical resistance properties of starch with little sacrifice in biodegradable behavior. GRAPHICAL ABSTRACT
摘要采用溶液插层法制备了镁铝层状双氧根修饰淀粉生物纳米复合材料(淀粉/层状双氧根)。利用傅里叶变换红外光谱、x射线衍射和高分辨率透射电子显微镜技术对生物纳米复合材料进行了系统的表征。淀粉的热稳定性由于层状双氢氧化物在淀粉基体内的分散而增强。淀粉基质中层状双氢氧化物的脱层使淀粉的耐化学性得到了很大的提高,但生物降解性能稍有降低。在此,层状双氢氧化物作为潜在的层压填料改变淀粉的结构、耐热性和耐化学性,而几乎不牺牲生物降解行为。图形抽象
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引用次数: 6
Editorial Board EOV 编辑委员会EOV
Q2 Materials Science Pub Date : 2018-10-10 DOI: 10.1080/03602559.2018.1458566
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引用次数: 0
Characterization of Polyurethane Grafted with Bis(2-hydroxyethyl) Terephthalate 对苯二甲酸双(2-羟乙基)接枝聚氨酯的表征
Q2 Materials Science Pub Date : 2018-09-22 DOI: 10.1080/03602559.2017.1410835
Yong-chan Chung, Sang Hyeon Kim, J. Choi, B. Chun
ABSTRACT Bis(2-hydroxyethyl) terephthalate (BHETPA) was grafted onto polyurethane (PU) to investigate the effects of BHETPA, which contains a rigid aromatic group and flexible hydroxyethyl groups, on the physical properties of PU. The cross-link density, viscosity, tensile strength, and shape recovery notably increased with an increase of BHETPA due to chemical cross-linking by BHETPA. A PU sample demonstrated excellent low-temperature flexibility compared with plain PU, showing complete recovery at approximately 0°C. Therefore, grafting BHETPA onto PU modified the thermal behavior and greatly improved the tensile stress, shape recovery, and low-temperature flexibility of PU compared to plain PU. GRAPHICAL ABSTRACT
摘要:将双(2-羟基乙基)对苯二甲酸酯(BHETPA)接枝到聚氨酯(PU)上,研究了含有刚性芳基和柔性羟乙基的BHETPA对PU物理性能的影响。由于BHETPA的化学交联作用,交联密度、粘度、抗拉强度和形状回复率随着BHETPA用量的增加而显著提高。与普通PU相比,PU样品表现出优异的低温柔韧性,在大约0°C时显示完全恢复。因此,与普通PU相比,接枝BHETPA改变了PU的热性能,大大提高了PU的拉伸应力、形状恢复和低温柔韧性。图形抽象
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引用次数: 1
期刊
Polymer-Plastics Technology and Engineering
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