Sustainable preparation of waste expanded polypropylene composites with green-synthesized Ag and graphite-derived carbon: characterization and UV/H₂O₂-assisted dye removal

IF 3.5 4区 化学 Q3 POLYMER SCIENCE
Huseyin Gumus, Semra Yılmazer Keskin, Emrah Bulut
{"title":"Sustainable preparation of waste expanded polypropylene composites with green-synthesized Ag and graphite-derived carbon: characterization and UV/H₂O₂-assisted dye removal","authors":"Huseyin Gumus,&nbsp;Semra Yılmazer Keskin,&nbsp;Emrah Bulut","doi":"10.1007/s10965-026-05108-w","DOIUrl":null,"url":null,"abstract":"<div><p>Waste plastics derived from petroleum sources pose a serious global challenge, and their recycling represents an effective strategy from both environmental and economic perspectives. Expanded polypropylene (EPP), widely used in various industrial sectors, is generated in considerable quantities as waste. Waste EPP was functionalized with green-synthesized Ag and thermally processed graphite-derived carbon to prepare flat-sheet composites via thermally induced phase separation (TIPS). The composites were characterized by XRD, SEM, FTIR, and TG-DSC analyses, and their adsorption and UV/H₂O₂-assisted dye removal performances were evaluated using methyl orange (MO) as a model pollutant. Adsorption efficiencies remained limited, reaching 10.5% for Ag-GO-EP and 9.6% for GO-EP. Under the final UV/H₂O₂ conditions, MO removal reached 32.2% for Ag-GO-EP and 30.8% for Ag-EP, with corresponding TOC mineralization values of 24.3% and 22.5%, respectively. Disk diffusion tests showed only limited antimicrobial response against E. coli O157:H7 and S. aureus. Ag-GO-EP maintained its dye removal performance over four consecutive cycles, with a decrease of &lt; 1% between cycles. These findings demonstrate that waste EPP can be converted into stable and reusable functional composites through a simple modification route, providing a potential approach for the functional valorization of polymer waste.</p></div>","PeriodicalId":658,"journal":{"name":"Journal of Polymer Research","volume":"33 9","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2026-09-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Research","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10965-026-05108-w","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

Waste plastics derived from petroleum sources pose a serious global challenge, and their recycling represents an effective strategy from both environmental and economic perspectives. Expanded polypropylene (EPP), widely used in various industrial sectors, is generated in considerable quantities as waste. Waste EPP was functionalized with green-synthesized Ag and thermally processed graphite-derived carbon to prepare flat-sheet composites via thermally induced phase separation (TIPS). The composites were characterized by XRD, SEM, FTIR, and TG-DSC analyses, and their adsorption and UV/H₂O₂-assisted dye removal performances were evaluated using methyl orange (MO) as a model pollutant. Adsorption efficiencies remained limited, reaching 10.5% for Ag-GO-EP and 9.6% for GO-EP. Under the final UV/H₂O₂ conditions, MO removal reached 32.2% for Ag-GO-EP and 30.8% for Ag-EP, with corresponding TOC mineralization values of 24.3% and 22.5%, respectively. Disk diffusion tests showed only limited antimicrobial response against E. coli O157:H7 and S. aureus. Ag-GO-EP maintained its dye removal performance over four consecutive cycles, with a decrease of < 1% between cycles. These findings demonstrate that waste EPP can be converted into stable and reusable functional composites through a simple modification route, providing a potential approach for the functional valorization of polymer waste.

绿色合成银和石墨衍生碳的废膨胀聚丙烯复合材料的可持续制备:表征和UV/H₂O₂辅助脱色
来自石油来源的废塑料构成了严重的全球挑战,从环境和经济的角度来看,它们的回收是一种有效的战略。膨胀聚丙烯(EPP)广泛用于各个工业部门,作为废物产生了相当数量。利用绿色合成的Ag和热处理的石墨衍生碳对废旧EPP进行功能化,通过热诱导相分离(TIPS)法制备了平板复合材料。采用XRD、SEM、FTIR和TG-DSC对复合材料进行了表征,并以甲基橙(MO)为模型污染物,评价了复合材料的吸附性能和UV/H₂O₂辅助脱色性能。Ag-GO-EP的吸附效率为10.5%,GO-EP的吸附效率为9.6%。在最终的UV/H₂O₂条件下,Ag-GO-EP的MO去除率达到32.2%,Ag-EP达到30.8%,相应的TOC矿化值分别为24.3%和22.5%。圆盘扩散试验显示对大肠杆菌O157:H7和金黄色葡萄球菌只有有限的抗菌反应。Ag-GO-EP在连续四个循环中保持了染料去除性能,循环之间下降了1%。这些发现表明,通过一种简单的改性途径,废旧EPP可以转化为稳定且可重复使用的功能复合材料,为聚合物废弃物的功能增值提供了一种潜在的途径。
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
Journal of Polymer Research
Journal of Polymer Research 化学-高分子科学
CiteScore
4.70
自引率
7.10%
发文量
472
审稿时长
3.6 months
期刊介绍: Journal of Polymer Research provides a forum for the prompt publication of articles concerning the fundamental and applied research of polymers. Its great feature lies in the diversity of content which it encompasses, drawing together results from all aspects of polymer science and technology. As polymer research is rapidly growing around the globe, the aim of this journal is to establish itself as a significant information tool not only for the international polymer researchers in academia but also for those working in industry. The scope of the journal covers a wide range of the highly interdisciplinary field of polymer science and technology, including: polymer synthesis; polymer reactions; polymerization kinetics; polymer physics; morphology; structure-property relationships; polymer analysis and characterization; physical and mechanical properties; electrical and optical properties; polymer processing and rheology; application of polymers; supramolecular science of polymers; polymer composites.
×
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:604180095
Book学术官方微信
小红书