Sonja Stojanov, Olga Govedarica, Marija Milanović, Julijana Žeravica, Berta Barta Hollo, Dragan Govedarica, Mirjana Jovičić
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Based on the obtained results, it is assumed that there is an interaction between the components of the curing system and the surface of the zeolite particle, and that is why the vulcanization reaction starts earlier with an increase in zeolite in the rubber mixture. This underscores the significant role of zeolite in accelerating the curing reaction of natural rubber-based compounds. The composites were vulcanized in a press at 150 °C for 15 min. The chemical structure was analyzed using FTIR, and the sample morphology was examined using SEM. The degree of swelling in toluene and distilled water was determined. The tensile strength values, modulus of elasticity at 100% and 300% elongation, and elongation at break were measured using a universal testing machine. Hardness was assessed according to the Shore A scale. With a small addition of zeolite (up to 10 phr), there is no significant change in the tensile strength values. 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引用次数: 0
摘要
沸石因其独特的结构和催化特性而闻名,我们将其添加到天然橡胶基体中,以研究其对硫化过程和复合材料性能的影响。天然橡胶基复合材料与 4A 合成沸石(0、5、10、15、20 和 30 phr)一起咀嚼。在 150 °C 的移动模流变仪上对橡胶化合物的固化进行了监测。还使用等温 DSC 方法研究了在 150 ℃、160 ℃ 和 170 ℃ 下的固化过程。根据获得的结果,可以推测硫化体系的成分与沸石颗粒表面之间存在相互作用,这就是为什么随着橡胶混合物中沸石含量的增加,硫化反应会提前开始。这说明了沸石在加速天然橡胶基化合物硫化反应中的重要作用。复合材料在 150 °C 的压力下硫化 15 分钟。使用傅立叶变换红外光谱分析了化学结构,并使用扫描电镜观察了样品的形态。测定了在甲苯和蒸馏水中的溶胀度。使用万能试验机测量了拉伸强度值、100% 和 300% 伸长率下的弹性模量以及断裂伸长率。硬度根据邵氏 A 级进行评估。在添加少量沸石(最多 10 phr)的情况下,拉伸强度值没有明显变化。然而,在天然橡胶基体中添加大量沸石会导致测试的机械性能下降。可以认为,复合材料中沸石 4A MS 的比例越大,机械性能就越差,因为孔隙率增加了。沸石的添加量会影响受检样品的热分解初始阶段,以及在 500 °C 温度下分析后的其余部分。
The Effect of Synthetic Zeolite on the Curing Process and the Properties of the Natural Rubber-Based Composites.
Zeolites, known for their unique structural and catalytic properties, are added to the natural rubber matrix to investigate their influence on the vulcanization process and the resultant properties of composites. The natural rubber-based composites were masticated with 4A synthetic zeolite (0, 5, 10, 15, 20, and 30 phr). The curing of the rubber compounds was monitored on a moving die rheometer at 150 °C. The isothermal DSC method was also used to study the curing process at 150 °C, 160 °C, and 170 °C. Based on the obtained results, it is assumed that there is an interaction between the components of the curing system and the surface of the zeolite particle, and that is why the vulcanization reaction starts earlier with an increase in zeolite in the rubber mixture. This underscores the significant role of zeolite in accelerating the curing reaction of natural rubber-based compounds. The composites were vulcanized in a press at 150 °C for 15 min. The chemical structure was analyzed using FTIR, and the sample morphology was examined using SEM. The degree of swelling in toluene and distilled water was determined. The tensile strength values, modulus of elasticity at 100% and 300% elongation, and elongation at break were measured using a universal testing machine. Hardness was assessed according to the Shore A scale. With a small addition of zeolite (up to 10 phr), there is no significant change in the tensile strength values. However, adding a considerable amount of zeolite to a natural rubber matrix results in a deterioration of the tested mechanical properties. It can be assumed that with large proportions of zeolite 4A MS in the composites, the mechanical properties deteriorated due to increased porosity. The amount of added zeolite affects the initial stages of thermal decomposition of the examined samples and the rest after the analysis at a temperature of 500 °C.
期刊介绍:
Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.