Reactive melt‐grafting of maleic anhydride onto olefin block copolymer toward high‐performance polar polyolefin thermoplastic elastomer

聚烯烃 马来酸酐 共聚物 弹性体 热塑性弹性体 材料科学 嫁接 烯烃纤维 复合材料 热塑性塑料 高分子化学 高分子科学 聚合物 图层(电子)
作者
Yu Kou,Yuqi Ma,Jialiang Li,Shilong Zhang,Jiaxun Cao,Hua Deng,Yanling Zhu,Yongsheng Zhao,Jianbin Qin,Guangcheng Zhang
出处
期刊:Polymer International [Wiley]
卷期号:73 (7): 545-555 被引量:9
标识
DOI:10.1002/pi.6627
摘要

Abstract The block structure of olefin block copolymer (OBC) elastomer gives it good elasticity and heat resistance relative to other polyolefin elastomers. However, the non‐polar nature of OBC chains limits its comprehensive properties like dyeing and toughening for polar engineering plastics. In this work, maleic anhydride (MA) and dicumyl peroxide (DCP) were selected as a typical polar monomer and a radical initiator to modify the polarity of OBC elastomer. During the melt‐grafting process, the DCP content was tuned to optimize the grafting efficiency while the MA‐to‐OBC ratio was fixed at 5 wt%. It was found that all the melt‐grafting reactions show high efficiency and can be finished in 3 min at 170 °C. With the increase of DCP content, the estimated grafting degree of OBC‐ g ‐MA elastomer increases from 0.40% to 1.16% along with increased gel content from 4.27% to 22.44%. A suitable grafting process was obtained with a DCP content of 3.0 wt% by balancing grafting efficiency and final mechanical properties. The optimized OBC‐ g ‐MA elastomer with a grafting degree of 0.92% has a mechanical strength of 17.15 MPa, a Young's modulus of 26.35 MPa, elongation of 1564% and strain recovery of 59.73%. Additionally, the contact angle test shows that polar grafting can increase surface hydrophilicity while excessive crosslinking promotes hydrophobicity. Therefore, our work has demonstrated the feasibility of the reactive melt‐grafting method to prepare OBC‐ g ‐MA elastomer and can also provide a processing reference for other chemical functionalization of polyolefin thermoplastic elastomers. © 2024 Society of Industrial Chemistry.
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
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
cliff发布了新的文献求助10
刚刚
平淡的天思完成签到,获得积分10
1秒前
1秒前
杨三月发布了新的文献求助10
3秒前
2211650110发布了新的文献求助10
3秒前
lili完成签到,获得积分10
3秒前
4秒前
nyh发布了新的文献求助10
4秒前
5秒前
8秒前
会举重的树完成签到,获得积分10
8秒前
12秒前
12秒前
Ov5发布了新的文献求助10
12秒前
椰子应助不是张国荣采纳,获得10
12秒前
13秒前
13秒前
zips完成签到,获得积分10
15秒前
16秒前
16秒前
syy发布了新的文献求助10
16秒前
17秒前
ywhys发布了新的文献求助10
17秒前
半糖糖发布了新的文献求助10
17秒前
上官若男应助why采纳,获得10
18秒前
Rr发布了新的文献求助10
18秒前
Iris完成签到,获得积分10
18秒前
汉堡包应助2211650110采纳,获得10
18秒前
li完成签到,获得积分10
18秒前
Hello应助邓邵斌采纳,获得10
18秒前
思源应助ningxiaotong采纳,获得10
18秒前
打打应助科研通管家采纳,获得10
18秒前
bkagyin应助高贵银耳汤采纳,获得10
19秒前
李健应助科研通管家采纳,获得10
19秒前
科研通AI2S应助cliff采纳,获得10
19秒前
大个应助科研通管家采纳,获得10
19秒前
彭于晏应助科研通管家采纳,获得10
19秒前
FashionBoy应助科研通管家采纳,获得10
19秒前
上官若男应助科研通管家采纳,获得10
20秒前
syyyyy完成签到,获得积分20
20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
HYDROLYSE ACIDE DE QUELQUES DIOXASPIROCYCLANES 1314
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Navigating Normative Orders. Interdisciplinary Perspectives 800
1 Peter and Christ's Descent to the Dead in Its Early Christian Reception 700
Organizational Behavior 510
Management and the Arts 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7749362
求助须知:如何正确求助?哪些是违规求助? 9297188
关于积分的说明 20238814
捐赠科研通 7330710
什么是DOI,文献DOI怎么找? 3309111
关于科研通互助平台的介绍 2460787
邀请新用户注册赠送积分活动 2321382