In situ emulsion polymerization of poly (vinyl acetate) and asparagus racemosus biopolymer composites for flexible energy storage applications

材料科学 复合材料 差示扫描量热法 乳液聚合 聚醋酸乙烯酯 醋酸乙烯酯 热重分析 复合数 扫描电子显微镜 原位聚合 玻璃化转变 动态力学分析 聚合物 聚合 化学工程 物理 工程类 热力学 共聚物
作者
M. T. Ramesan,T. P. Sameela,K. Meera,Bijal Kottukkal Bahuleyan,Meenakshi Verma
出处
期刊:Polymer Composites [Wiley]
卷期号:44 (7): 4168-4177 被引量:13
标识
DOI:10.1002/pc.27388
摘要

Abstract Polymer composites reinforced with synthetic materials are losing acceptability due to significant environmental concerns and high costs. Natural fillers are becoming increasingly popular due to their non‐toxicity, lightweight, low energy consumption, and environmental friendliness. In the present work, poly (vinyl acetate) (PVAc) and asparagus racemosus (AR) bio‐composites have been prepared by an in‐situ emulsion polymerization method. The composite films were subsequently examined by Fourier transform infrared spectroscopy (FT‐IR), X‐ray diffraction, atomic force microscopy (AFM), field emission scanning electron microscopy (FE‐SEM), optical microscope, differential scanning calorimeter (DSC), and thermogravimetric analysis. The formation of AR in PVAc composite was confirmed by the characteristic AR band at 3300 cm −1 in FT‐IR spectra. X‐ray diffraction studies showed a shift in the amorphous peak of PVAc/AR composites compared to pure PVAc. The AFM, FE‐SEM, and optical microscopic results revealed the uniform distribution of AR in the polymer matrix. DSC and TGA measurements showed that the glass transition temperature and thermal stability of PVAc increased with the inclusion of bio‐filler. The tensile strength, hardness, dielectric constant and AC conductivity of PVAc were observed to increases with boehmite inclusion, whereas elongation at break is reduced. As a result, environmentally friendly PVAc/AR composites with good mechanical, thermal and electrical properties could be a viable green substitute for energy storage, flexible electronic, and other electrochemical devices.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
852应助科研通管家采纳,获得10
刚刚
烟花应助科研通管家采纳,获得10
刚刚
寻道图强应助科研通管家采纳,获得50
刚刚
薯薯完成签到,获得积分10
刚刚
思源应助科研通管家采纳,获得10
刚刚
orixero应助科研通管家采纳,获得10
刚刚
苗条而大河完成签到,获得积分10
刚刚
科研通AI6应助科研通管家采纳,获得10
刚刚
科研通AI6应助科研通管家采纳,获得10
刚刚
在水一方应助科研通管家采纳,获得10
刚刚
小Y应助科研通管家采纳,获得20
刚刚
Zx_1993应助科研通管家采纳,获得10
1秒前
晚若旧完成签到,获得积分10
1秒前
avalanche应助科研通管家采纳,获得20
1秒前
李爱国应助科研通管家采纳,获得10
1秒前
小马甲应助科研通管家采纳,获得10
1秒前
Owen应助科研通管家采纳,获得10
1秒前
wanci应助科研通管家采纳,获得10
1秒前
科研通AI6应助科研通管家采纳,获得10
1秒前
1秒前
在水一方应助科研通管家采纳,获得10
1秒前
隐形曼青应助科研通管家采纳,获得10
1秒前
科研通AI6应助科研通管家采纳,获得10
1秒前
Orange应助科研通管家采纳,获得30
1秒前
科研乞丐应助科研通管家采纳,获得20
1秒前
1秒前
吃定彩虹发布了新的文献求助10
2秒前
雪雪啊发布了新的文献求助30
2秒前
2秒前
3秒前
淡淡夕阳发布了新的文献求助10
3秒前
3秒前
3秒前
洁净的亦竹完成签到 ,获得积分10
3秒前
浮游应助Rainstorm27采纳,获得10
3秒前
可爱千兰完成签到,获得积分10
3秒前
天天快乐应助刻苦的如霜采纳,获得10
3秒前
4秒前
4秒前
量子星尘发布了新的文献求助10
4秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Social Work Ethics Casebook: Cases and Commentary (revised 2nd ed.).. Frederic G. Reamer 1070
The Complete Pro-Guide to the All-New Affinity Studio: The A-to-Z Master Manual: Master Vector, Pixel, & Layout Design: Advanced Techniques for Photo, Designer, and Publisher in the Unified Suite 1000
按地区划分的1,091个公共养老金档案列表 801
The International Law of the Sea (fourth edition) 800
Machine Learning for Polymer Informatics 500
A Guide to Genetic Counseling, 3rd Edition 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 物理化学 基因 遗传学 催化作用 冶金 量子力学 光电子学
热门帖子
关注 科研通微信公众号,转发送积分 5410122
求助须知:如何正确求助?哪些是违规求助? 4527656
关于积分的说明 14112011
捐赠科研通 4442051
什么是DOI,文献DOI怎么找? 2437805
邀请新用户注册赠送积分活动 1429747
关于科研通互助平台的介绍 1407769