Fabrication and thermomechanical property investigations of polypropylene/silica and polypropylene/modified silica composite films

Özkan Demirbas , Hasan Cetin , Mehmet Salih NAS , Mehmet Harbi Calimli , Ramazan Bayat , Fatih Sen
{"title":"Fabrication and thermomechanical property investigations of polypropylene/silica and polypropylene/modified silica composite films","authors":"Özkan Demirbas ,&nbsp;Hasan Cetin ,&nbsp;Mehmet Salih NAS ,&nbsp;Mehmet Harbi Calimli ,&nbsp;Ramazan Bayat ,&nbsp;Fatih Sen","doi":"10.1016/j.nxmate.2024.100357","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, we fabricated polypropylene/silica (PP/S) and polypropylene/modified silica (PP/MS) composite films using the extrusion technique, and characterized, and investigated their thermomechanical behaviors. The characterization of the neat materials and prepared composites was successfully conducted using some advanced spectroscopic techniques. The thermal stability and thermomechanical behaviors of the composites were investigated through thermogravimetry analysis (TGA) and dynamic mechanical analysis (DMA). The tensile tests revealed that the PP/MS composites exhibited the highest strength values, reaching 22.23 MPa with 1.0 % MS. Higher tensile strength was obtained with PP/MS composites compared to PP/S composites, proving the clear effect of the hexadecyltrimethylammonium bromide (HTAB) binder in the composition of the composites. The highest strength values obtained with the PP/S composites were 20.10 MPa at a ratio of 2.5 %.</p></div>","PeriodicalId":100958,"journal":{"name":"Next Materials","volume":"7 ","pages":"Article 100357"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2949822824002545/pdfft?md5=299828b05c79d9967a1c49b433361d42&pid=1-s2.0-S2949822824002545-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949822824002545","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In this study, we fabricated polypropylene/silica (PP/S) and polypropylene/modified silica (PP/MS) composite films using the extrusion technique, and characterized, and investigated their thermomechanical behaviors. The characterization of the neat materials and prepared composites was successfully conducted using some advanced spectroscopic techniques. The thermal stability and thermomechanical behaviors of the composites were investigated through thermogravimetry analysis (TGA) and dynamic mechanical analysis (DMA). The tensile tests revealed that the PP/MS composites exhibited the highest strength values, reaching 22.23 MPa with 1.0 % MS. Higher tensile strength was obtained with PP/MS composites compared to PP/S composites, proving the clear effect of the hexadecyltrimethylammonium bromide (HTAB) binder in the composition of the composites. The highest strength values obtained with the PP/S composites were 20.10 MPa at a ratio of 2.5 %.

聚丙烯/二氧化硅和聚丙烯/改性二氧化硅复合薄膜的制作和热力学特性研究
在这项研究中,我们采用挤压技术制作了聚丙烯/二氧化硅(PP/S)和聚丙烯/改性二氧化硅(PP/MS)复合薄膜,并对其热力学行为进行了表征和研究。利用一些先进的光谱技术成功地对纯材料和制备的复合材料进行了表征。通过热重分析(TGA)和动态力学分析(DMA)研究了复合材料的热稳定性和热力学行为。拉伸试验表明,PP/MS 复合材料的强度值最高,在含有 1.0 % MS 的情况下达到 22.23 兆帕。与 PP/S 复合材料相比,PP/MS 复合材料获得了更高的拉伸强度,这证明了复合材料成分中十六烷基三甲基溴化铵(HTAB)粘合剂的明显效果。PP/S 复合材料的最高强度值为 20.10 兆帕,比例为 2.5%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信