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Influence of CNTs on the gradient phase structure formed by the layered resin structure used to model the interlaminar region of interleaved FRPs CNT 对用于模拟交错玻璃钢层间区域的层状树脂结构所形成的梯度相结构的影响
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-30 DOI: 10.1515/polyeng-2023-0232
Jiawei Yao, Yuekun Sun, Yifan Niu
The interleaved fiber-reinforced polymer composites (FRPs) by carbon nanotubes (CNTs)/thermoplastic polyetherketone-cardo (PEK-C) hybrid interleaves show the potential of comprehensively improving the mechanical properties of composites and have been hotspot. However, the synergistic effect and mechanism of CNTs and TP resin have not been attained. The interlaminar region of interleaved composites is too narrow and complex to be fully analyzed. Therefore, the layered resin structure composed of an interlayer and a matrix (epoxy) layer was prepared to model the interlaminar region in this study. The evolution of gradient structure developed by the layered structure in curing and the influence of presence of CNTs in interlayer were investigated based on morphology characterization. The results showed that epoxy resin gradually diffused into the interlayer, resulting in the concentration gradient and the resultant gradient phase structure. The presence of CNTs in hybrid interlayer hindered the resin diffusion and consequently hindered the formation of dual-phase structure, which was not conducive to the toughness improvement. The inappropriate high temperature was not recommended due to the effect of facilitating diffusion, probably resulting in the formation of excrescent epoxy layer in the interlaminar region and undesired mechanical performance. This study conducted experiments on resin system to simplify the interesting subject and the results will help to develop the synergistic mechanism of TP resin and nanoparticles.
碳纳米管(CNTs)/热塑性聚醚酮-卡多(PEK-C)混合交错纤维增强聚合物复合材料(FRPs)具有全面改善复合材料力学性能的潜力,一直是研究的热点。然而,CNTs 与 TP 树脂的协同效应和机理尚未得到研究。交错复合材料的层间区域过于狭窄和复杂,无法进行全面分析。因此,本研究制备了由中间层和基体(环氧树脂)层组成的层状树脂结构来模拟层间区域。基于形貌表征,研究了层状结构在固化过程中形成的梯度结构的演变,以及夹层中存在 CNTs 的影响。结果表明,环氧树脂逐渐扩散到夹层中,形成了浓度梯度和梯度相结构。混合夹层中 CNT 的存在阻碍了树脂的扩散,进而阻碍了双相结构的形成,不利于韧性的提高。由于促进扩散的作用,不建议使用不适当的高温,这很可能导致在层间区域形成脱落的环氧层,从而影响力学性能。本研究对树脂系统进行了实验,以简化这一有趣的课题,其结果将有助于发展 TP 树脂与纳米粒子的协同机制。
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引用次数: 0
Biopolymer-based nanocomposites for application in biomedicine: a review 基于生物聚合物的纳米复合材料在生物医学中的应用:综述
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-27 DOI: 10.1515/polyeng-2023-0166
Abdul Aziz Shaikh, Preetam Datta, Prithwish Dastidar, Arkadip Majumder, Maharghya Dyuti Das, Pratikrit Manna, Subhasis Roy
Biopolymer-based nanocomposites have gained significant attention in biomedicine due to their unique properties and potential applications. These nanocomposites combine biopolymers, natural polymers derived from renewable sources, with nanoparticles or other nanoscale materials to create materials with enhanced properties and functionalities. Biopolymers that are used to make bio-nanocomposites are cellulose, alginate, chitosan, starch, polylactic acid (PLA), polyhydroxyalkanoate (PHA), polyhydroxybutyrate (PHB), etc. These have different properties, and they can be used in several types of treatments. Scaffolds frequently employ polylactic acid-gelatin, nanocellulose, and chitosan. Studies have shown that some special types of hydrogel films have proven beneficial in anticancer treatment. Synthetic and naturally occurring substances such as PLA, polyvinyl alcohol (PVA), guar gum, and chitosan are employed in the drug delivery system. Nanocomposites such as silver nanoparticles with chitosan, sulfated polysaccharides, and thyme-loaded carrot nanocellulose or starch biopolymer nanocomposites have been used to stop bacterial development. This review article provides a comprehensive insight into biopolymer-based nanocomposites and their uses. Also, it has been incorporated into fields such as biosensors, bioimaging, blood clotting, immunomodulation, antibacterial and antiviral drugs, and food packaging. Hence, the primary objective of this review is to provide an overall perspective on biopolymer nanocomposites in nanomedicine.
基于生物聚合物的纳米复合材料因其独特的性能和潜在的应用而在生物医学领域备受关注。这些纳米复合材料将生物聚合物(从可再生资源中提取的天然聚合物)与纳米粒子或其他纳米级材料结合在一起,创造出具有更强特性和功能的材料。用于制造生物纳米复合材料的生物聚合物有纤维素、海藻酸、壳聚糖、淀粉、聚乳酸(PLA)、聚羟基烷酸(PHA)、聚羟基丁酸(PHB)等。这些材料具有不同的特性,可用于多种类型的治疗。支架经常使用聚乳酸明胶、纳米纤维素和壳聚糖。研究表明,一些特殊类型的水凝胶薄膜已被证明有利于抗癌治疗。在给药系统中使用了聚乳酸、聚乙烯醇(PVA)、瓜尔豆胶和壳聚糖等合成和天然物质。银纳米粒子与壳聚糖、硫酸化多糖、百里香负载胡萝卜纳米纤维素或淀粉生物聚合物纳米复合材料等纳米复合材料已被用于阻止细菌发展。这篇综述文章全面介绍了基于生物聚合物的纳米复合材料及其用途。此外,它还被应用于生物传感器、生物成像、血液凝固、免疫调节、抗菌和抗病毒药物以及食品包装等领域。因此,本综述的主要目的是提供有关纳米医学中生物聚合物纳米复合材料的整体观点。
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引用次数: 0
Stiff, strong, and tear-resistant physical hydrogels with widely tunable toughness by post-treatments 硬度高、强度大、抗撕裂的物理水凝胶,其韧性可通过后处理进行广泛调整
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-19 DOI: 10.1515/polyeng-2023-0134
Yu Zhao, Bing Hu Xia, Lei Wang, Yang Liu, Lei Zu, Hui Qin Lian, Xiu Guo Cui, Hao Wang
Synthetic polymeric hydrogel is a potential substitute for soft biological tissues. However, the poor mechanical properties of traditional synthetic hydrogels limit their applications in biological fields. Herein, a series of tough physical hydrogels have been prepared by micellar polymerization, in the existence of sodium bromide (NaBr), using methacrylic acid (MA) and stearyl acrylate (SA) as monomers, cetyltrimethyl ammonium bromide (CTAB) as cationic surfactant. The hydrogels exhibit excellent mechanical properties: modulus, toughness, and tearing fracture energy up to 7.8 MPa, 34 MJ m−3, and 16,600 J m−2, respectively. Moreover, it was found that the toughness of the hydrogels can be modulated in a very wide range by different post-treatments, e.g., dried/reswelling, freezing/thawing, or heated treatments. After post-treatments, the elastic physical hydrogels even turn into brittle plastics: modulus and toughness vary by 3 and 4 orders of magnitude, respectively. The mechanism for this wide tunability is attributed to the change of electrostatic attraction, crystallization, and phase separation during post-treatments.
合成聚合物水凝胶是软生物组织的潜在替代品。然而,传统合成水凝胶的机械性能较差,限制了其在生物领域的应用。本文以甲基丙烯酸(MA)和丙烯酸硬脂酯(SA)为单体,十六烷基三甲基溴化铵(CTAB)为阳离子表面活性剂,在溴化钠(NaBr)存在的条件下通过胶束聚合制备了一系列韧性物理水凝胶。水凝胶表现出优异的机械性能:模量、韧性和撕裂断裂能分别高达 7.8 MPa、34 MJ m-3 和 16,600 J m-2。此外,研究还发现,水凝胶的韧性可通过不同的后处理(如干燥/膨胀、冷冻/解冻或加热处理)在很大范围内进行调节。经过后处理后,弹性物理水凝胶甚至会变成脆性塑料:模量和韧性分别会有 3 个和 4 个数量级的变化。这种广泛可调性的机理归因于后处理过程中静电吸引、结晶和相分离的变化。
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引用次数: 0
Numerical investigation of the strength of Al/GFRP adhesive bonding under tensile loading 拉伸荷载下铝/玻璃纤维增强塑料粘接强度的数值研究
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-10 DOI: 10.1515/polyeng-2023-0273
Mohammad Reza Samadi, Mohammad Hossein Alaei, Jafar Eskandari Jam
In this study, adhesive bonding of aluminum (Al) to glass fiber reinforced polymer (GFRP) was investigated using finite element analysis to optimize bond strength. Mechanical surface preparation has a great influence on the chemical properties (increasing surface energy and creating a stronger bond) and mechanical properties (creating mechanical interlocking and increasing friction) of adhesive bonding. Hence, the response surface method was employed to examine the influence of groove number (1, 3, 5), groove angle (0, 45, 90°), groove shape (V-shape, square, concave), and joint type (metal–metal, metal–composite, composite–composite) on the tensile strength of the bond. To simulate the bond behavior of Al/GFRP under different parameter conditions, the cohesive zone model was used to consider the crack growth. Optimization results obtained by the desirability function method showed that the maximum bond strength was achieved with a groove number of 1, groove shape of square, groove angle of 0°, and metal–metal joint type. The optimization results predicted by the desirability function and finite element analysis were in good agreement with those obtained by experimental tests.
本研究采用有限元分析法研究了铝(Al)与玻璃纤维增强聚合物(GFRP)的粘接,以优化粘接强度。机械表面处理对粘合剂粘接的化学特性(增加表面能并产生更强的粘接)和机械特性(产生机械互锁并增加摩擦)有很大影响。因此,我们采用响应面法研究了沟槽数量(1、3、5)、沟槽角度(0、45、90°)、沟槽形状(V 形、方形、凹形)和连接类型(金属-金属、金属-复合材料、复合材料-复合材料)对粘接拉伸强度的影响。为了模拟铝/玻璃纤维增强塑料在不同参数条件下的粘接行为,使用了内聚区模型来考虑裂纹的生长。通过理想函数法获得的优化结果表明,沟槽数量为 1、沟槽形状为正方形、沟槽角度为 0°、金属-金属连接类型时,粘接强度最大。由可取函数和有限元分析预测的优化结果与实验测试结果十分吻合。
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引用次数: 0
Study on the influence of in-mold sequential injection molding process parameters on mechanical properties of self-reinforced single composites 模内连续注塑成型工艺参数对自增强单一复合材料机械性能影响的研究
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-10 DOI: 10.1515/polyeng-2023-0230
Yong Lu, Chen Wang
In this paper, the self-reinforced single polymer composites (SR-SPCs) with different mechanical properties were obtained by compound injection molding technology, and the micro-morphology of these samples was observed. Then, using structured statistical methods, analysis of variance, and response surface methodology, study the effects of various molding variables on material morphology and properties and determine the most important molding variables and their interactions. Finally, the associated experimental data are fitted by the least squares minimization program, and the relevant dimensionless equations are obtained. The purpose is to objectively analyze the influence mechanism of molding parameters on SR-SPCs and establish a mechanism model. It was found that temperature change was the most important factor affecting the morphology and mechanical properties. The degree of molecular orientation is the most important factor to determine the tensile strength and elastic modulus of the sample. The change of crystallinity is the most important factor related to the elongation at break. By establishment relevant dimensionless equations, the influence of molding parameters on the mechanical properties of SR-SPCs, such as tensile strength and elastic modulus, was preliminarily studied.
本文通过复合注射成型技术获得了具有不同力学性能的自增强单体聚合物复合材料(SR-SPCs),并观察了这些样品的微观形态。然后,利用结构统计方法、方差分析和响应面方法,研究各种成型变量对材料形态和性能的影响,并确定最重要的成型变量及其相互作用。最后,利用最小二乘最小化程序对相关实验数据进行拟合,得到相关的无量纲方程。目的是客观分析成型参数对 SR-SPC 的影响机理,并建立机理模型。研究发现,温度变化是影响形貌和机械性能的最重要因素。分子取向度是决定样品拉伸强度和弹性模量的最重要因素。结晶度的变化是与断裂伸长率相关的最重要因素。通过建立相关的无量纲方程,初步研究了成型参数对拉伸强度和弹性模量等 SR-SPC 力学性能的影响。
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引用次数: 0
Preparation, characterization, and application of fluorinated acrylate copolymer for the conservation of stone building heritages in Putuo Zongcheng Temple, China 含氟丙烯酸酯共聚物在中国普陀宗乘之庙石质建筑文物保护中的制备、表征和应用
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-04 DOI: 10.1515/polyeng-2023-0158
Zhiyong Wu, Chuang Ma, Qinghe Niu, Caiwu Wu, Ye Wang
To prevent the weathering deterioration of stone building heritages in Putuo Zongcheng Temple, the fluorinated acrylate copolymer was prepared with methyl methacrylate, n-butyl acrylate, and 2,2,3,4,4,4-hexafluorobutyl methacrylate as monomers. The structure and surface morphology of the copolymer were described by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). The antiaging of the copolymer was studied by the ultraviolet aging test; the contact angle and imbibition spontaneous tests were performed to estimate the wettability alteration of the copolymer emulsion. Results show that the fluorinated copolymer with 32.54 % HFMA content possesses optimal aging resistance and superb hydrophobicity. The contact angles of coated samples range from 96.90° to 125.80°. Considering the influence of water on rock weathering, the fluorinated copolymer coating is a potential method to avoid the degrading of stone heritages.
为防止普陀宗乘之庙石质建筑文物风化劣化,以甲基丙烯酸甲酯、丙烯酸正丁酯和甲基丙烯酸 2,2,3,4,4,4-六氟丁酯为单体,制备了含氟丙烯酸酯共聚物。傅立叶变换红外光谱(FTIR)和扫描电子显微镜(SEM)对共聚物的结构和表面形态进行了描述。紫外老化试验研究了共聚物的抗老化性;接触角和浸润自发试验估测了共聚物乳液的润湿性变化。结果表明,HFMA 含量为 32.54% 的氟化共聚物具有最佳的耐老化性和超强的疏水性。涂层样品的接触角在 96.90° 至 125.80° 之间。考虑到水对岩石风化的影响,氟化共聚物涂层是一种避免石质文物退化的潜在方法。
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引用次数: 0
CsxWO3-doped PEG/sweet potato form-stable composites for light-thermal conversion and energy storage 用于光热转换和能量存储的掺杂 CsxWO3 的 PEG/红薯形稳复合材料
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2024-01-03 DOI: 10.1515/polyeng-2023-0256
Yan Zhou, Xiangdong Liu, Dekun Sheng, Yuming Yang
Cesium tungsten bronze (CsxWO3)-doped PEG/sweet potato form-stable composites are fabricated through a facile two-step method of lyophilization and vacuum impregnation. Abundant starch microsphere enhances the PEG loading capacity above 72 % and also supplies capillary force as well as hydrogen bonding to improve the form-stability of the composites. Here, the latent heat, relative crystallinity (Xc), and light-thermal conversion efficiency of the system with 0.99 wt% CsxWO3 reach to 137.7 J/g, 97.7 %, and 83.5 %, respectively. The light-thermal conversion efficiency increases from 64.3 % to 91.1 % with 2.00 wt% CsxWO3. Besides, the composites exhibit improved thermal stability and excellent thermal reliability. The prepared bio-based composites with low-cost have broad application prospects in the field of energy storage.
通过冻干和真空浸渍两个步骤的简便方法,制备出了掺杂铯钨青铜(CsxWO3)的 PEG/甘薯形态稳定复合材料。丰富的淀粉微球提高了 PEG 的负载能力,使其超过 72%,同时还提供了毛细管力和氢键,从而提高了复合材料的成型稳定性。在这里,含 0.99 wt% CsxWO3 的体系的潜热、相对结晶度 (Xc) 和光热转换效率分别达到 137.7 J/g、97.7 % 和 83.5 %。2.00 wt% CsxWO3 的光热转换效率从 64.3 % 提高到 91.1 %。此外,复合材料还具有更好的热稳定性和出色的热可靠性。所制备的生物基复合材料成本低廉,在储能领域具有广阔的应用前景。
{"title":"CsxWO3-doped PEG/sweet potato form-stable composites for light-thermal conversion and energy storage","authors":"Yan Zhou, Xiangdong Liu, Dekun Sheng, Yuming Yang","doi":"10.1515/polyeng-2023-0256","DOIUrl":"https://doi.org/10.1515/polyeng-2023-0256","url":null,"abstract":"Cesium tungsten bronze (CsxWO<jats:sub>3</jats:sub>)-doped PEG/sweet potato form-stable composites are fabricated through a facile two-step method of lyophilization and vacuum impregnation. Abundant starch microsphere enhances the PEG loading capacity above 72 % and also supplies capillary force as well as hydrogen bonding to improve the form-stability of the composites. Here, the latent heat, relative crystallinity (Xc), and light-thermal conversion efficiency of the system with 0.99 wt% CsxWO<jats:sub>3</jats:sub> reach to 137.7 J/g, 97.7 %, and 83.5 %, respectively. The light-thermal conversion efficiency increases from 64.3 % to 91.1 % with 2.00 wt% CsxWO<jats:sub>3</jats:sub>. Besides, the composites exhibit improved thermal stability and excellent thermal reliability. The prepared bio-based composites with low-cost have broad application prospects in the field of energy storage.","PeriodicalId":16881,"journal":{"name":"Journal of Polymer Engineering","volume":"1 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2024-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139082570","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reviewer acknowledgement Journal of Polymer Engineering volume 43 (2023) 审稿人致谢 《聚合物工程学报》第 43 卷(2023 年)
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2023-12-19 DOI: 10.1515/polyeng-2023-0282
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引用次数: 0
Enhancement of the tribological and thermal properties of UHMWPE based ternary nanocomposites containing graphene and titanium titride 增强含有石墨烯和氮化钛的超高分子量聚乙烯基三元纳米复合材料的摩擦学性能和热性能
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2023-12-11 DOI: 10.1515/polyeng-2023-0182
Uwa O. Uyor, Abimbola P. I. Popoola, Olawale M. Popoola
Ultra-high molecular weight polyethylene (UHMWPE) generally does not have high resistance to wear and are characterised by poor thermal stability when exposed to long working condition. To address these shortcomings, this study used hybrid graphene nanoplatelets (GN) and titanium nitride (TiN) nanoparticles to significantly enhance the wear resistance and thermal stability of UHMWPE. The nanocomposites were prepared by solvent mixing and hot compression process. Scanning electron microscope showed uniform dispersion of the nanoparticles in the UHMWPE matrix. The developed UHMWPE showed improved wear resistance and thermal stability relative to the pure UHMWPE. For instance, the wear rate reduced from 6.7 × 10−3 mm3 N−1 m−1 and 3.67 × 10−2 mm3 N−1 m−1 for pure UHMWPE to 2.687 × 10−5 mm3 N−1 m−1 and 1.34 × 7 × 10−4 mm3 N−1 m−1 for UHMWPE–2 wt% GN–10 wt% TiN at applied loads of 10 N and 20 N respectively. This is about 100 % increment in wear resistance at the respective applied loads compared to the pure UHMWPE. The thermal stability of the fabricated nanocomposites was studied using the thermogravimetric analyser (TGA). The addition of nanoparticles significantly reduced the thermal decomposition of UHMWPE matrix. The enhanced properties of the UHMWPE–GN–TiN nanocomposites may be attributed to the network structures formed from the dispersion of the GN and TiN nanoparticles in the UHMWPE matrix with promoted molecular chains interlocking.
超高分子量聚乙烯(UHMWPE)的耐磨性通常不高,而且在长期工作条件下热稳定性较差。针对这些缺点,本研究采用混合石墨烯纳米片(GN)和氮化钛(TiN)纳米颗粒来显著提高超高分子量聚乙烯的耐磨性和热稳定性。纳米复合材料是通过溶剂混合和热压工艺制备的。扫描电子显微镜显示纳米粒子均匀地分散在超高分子量聚乙烯基体中。与纯超高分子量聚乙烯相比,所开发的超高分子量聚乙烯具有更好的耐磨性和热稳定性。例如,在施加 10 N 和 20 N 负载时,UHMWPE-2 wt% GN-10 wt% TiN 的磨损率分别从纯 UHMWPE 的 6.7 × 10-3 mm3 N-1 m-1 和 3.67 × 10-2 mm3 N-1 m-1 降低到 2.687 × 10-5 mm3 N-1 m-1 和 1.34 × 7 × 10-4 mm3 N-1 m-1。与纯超高分子量聚乙烯相比,在相应载荷下的耐磨性提高了约 100%。使用热重分析仪(TGA)研究了纳米复合材料的热稳定性。纳米颗粒的加入大大降低了超高分子量聚乙烯基体的热分解。超高分子量聚乙烯-GN-TiN 纳米复合材料性能的增强可能是由于 GN 和 TiN 纳米粒子在超高分子量聚乙烯基体中的分散形成了网络结构,促进了分子链的交锁。
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引用次数: 0
Morphologies, structures, and properties on blends of triblock copolymers and linear low-density polyethylene 三嵌段共聚物与线性低密度聚乙烯混合物的形态、结构和性能
IF 2 4区 工程技术 Q4 POLYMER SCIENCE Pub Date : 2023-12-08 DOI: 10.1515/polyeng-2023-0167
Ying Wang, Shangfeng Wu, Li-Zhi Liu, Hao Chen, Yuanxia Wang, Lixin Song, Ying Shi
Focusing on the study of the phase separation behavior of triblock copolymer and linear low-density polyethylene (LLDPE) systems helps to understand the influence of microstructure on the properties of poly(vinylcyclohexane)-b- poly(ethylene)-b-poly(vinylcyclohexane) (PVCH-PE-PVCH/LLDPE) blends. We prepared a series of blends of LLDPE and PVCH-PE-PVCH and explained their compatibility from the microstructure. The research findings indicate that despite having similar block compositions, PVCH-PE-PVCH with a higher molecular weight exhibits significantly stronger phase separation and crystallization ability compared to PVCH-PE-PVCH with lower molecular weight. In PVCH-PE-PVCH/LLDPE blends, the addition of 10 %, 20 %, and 30 % LLDPE induces earlier crystallization and crystal phase separation of polyethylene (PE) fragments. In addition, compared to the lower molecular weight of PVCH-PE-PVCH, the higher molecular weight of PVCH-PE-PVCH exhibits a higher tendency for independent crystallization and shows significant crystal phase separation during the cooling crystallization process when blended with LLDPE. The PE segments in the lower molecular weight of PVCH-PE-PVCH can more easily enter the nanoscale domain of LLDPE. Impact fracture electron microscopy also reveals better compatibility between the lower molecular weight of PVCH-PE-PVCH and LLDPE compared to the higher molecular weight of PVCH-PE-PVCH. Furthermore, the blends of lower molecular weight of PVCH-PE-PVCH and LLDPE exhibit a greater growth rate in elongation at break.
重点研究三嵌段共聚物和线性低密度聚乙烯(LLDPE)体系的相分离行为有助于了解微观结构对聚(乙烯基环己烷)-b-聚(乙烯)-b-聚(乙烯基环己烷)(PVCH-PE-PVCH/LLDPE)共混物性能的影响。我们制备了一系列 LLDPE 和 PVCH-PE-PVCH 的共混物,并从微观结构上解释了它们的相容性。研究结果表明,尽管具有相似的嵌段组成,但与分子量较低的 PVCH-PE-PVCH 相比,分子量较高的 PVCH-PE-PVCH 表现出更强的相分离和结晶能力。在 PVCH-PE-PVCH/LLDPE混合物中,添加 10%、20% 和 30% 的 LLDPE 会促使聚乙烯(PE)片段提前结晶和晶相分离。此外,与分子量较低的 PVCH-PE-PVCH 相比,分子量较高的 PVCH-PE-PVCH 在与 LLDPE 混合时,表现出更高的独立结晶趋势,并在冷却结晶过程中出现明显的晶相分离。分子量较低的 PVCH-PE-PVCH 中的 PE 段更容易进入 LLDPE 的纳米级域。冲击断裂电子显微镜还显示,与较高分子量的 PVCH-PE-PVCH 相比,较低分子量的 PVCH-PE-PVCH 与 LLDPE 的相容性更好。此外,较低分子量的 PVCH-PE-PVCH 和 LLDPE 的混合物在断裂伸长率方面表现出更高的增长率。
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引用次数: 0
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Journal of Polymer Engineering
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