Preparation and characterization of poly(ethylene terephthalate) copolyesters and fibers modified with sodium-5-sulfo-bis-(hydroxyethyl)-isophthalate and poly(ethylene glycol)

材料科学 差示扫描量热法 结晶度 高分子化学 玻璃化转变 聚酯纤维 乙二醇 阳离子聚合 乙烯 化学工程 热重分析 复合材料 聚合物 有机化学 化学 催化作用 物理 工程类 热力学
作者
Mingliang Zhao,Xueli Wang,Jianyong Yu
出处
期刊:Journal of The Textile Institute [Informa]
卷期号:107 (10): 1284-1295 被引量:12
标识
DOI:10.1080/00405000.2015.1101241
摘要

New copolyesters were successfully prepared with SIPE and PEG units designated as cationic dyeable polyester and easy cationic dyeable polyester. The number average molecular weight of PEG unit is 6000 (abbreviated as PEG6000). Corresponding copolyesters were spun into fibers with melt spinning method. Chemical and crystalline structures were characterized by the NMR and WAXD measurement, and thermal properties were tested by Differential Scanning Calorimetry and Thermogravimetric Analysis, respectively. NMR experimental results indicated the actual molar ratio of comonomers was basically consistent with the correlative feed ratio. WAXD results showed that crystalline structures of prepared copolyesters were similar to that of Poly(ethylene terephthalate). Moreover, the glass transition temperature, melting temperature, and thermal degradation temperature were found to decrease with the increase in weight ratio of PEG6000 units since the incorporation of higher PEG6000 content brought more ether bonds into molecular chains, which increased the asymmetry and irregularity of molecular chains and led to lower crystallinity. Besides, when content of PEG6000 increased, the breaking tenacity and initial modulus were reduced, yet elongation at break enhanced. It suggested that PEG6000 segments reduced the symmetry of molecular chains and decreased the orientation degree of fibers. In addition, because the incorporation of higher weight percentage of PEG6000 led to more hydroxyl end groups and ether bonds in molecular chains, the moisture regain of fibers increased, manifesting fibers had better hydrophilicity with increasing weight ratio of PEG6000 components.
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
镜子发布了新的文献求助10
2秒前
你的头发乱了完成签到,获得积分10
3秒前
Owen应助flsqw采纳,获得10
3秒前
griffon完成签到,获得积分10
3秒前
znlion发布了新的文献求助10
4秒前
李雯鑫发布了新的文献求助10
4秒前
wd123完成签到,获得积分20
4秒前
jjsss完成签到,获得积分10
4秒前
4秒前
斯文败类应助我爱科研采纳,获得10
4秒前
桐桐应助SWZ采纳,获得20
4秒前
euphoria发布了新的文献求助10
4秒前
英姑应助夏林采纳,获得20
4秒前
4秒前
华仔应助顺利亦凝采纳,获得10
5秒前
丁二完成签到,获得积分10
5秒前
5秒前
5秒前
温暖的白昼完成签到,获得积分10
5秒前
情怀应助花与海采纳,获得10
6秒前
楼谷秋发布了新的文献求助10
6秒前
6秒前
yin完成签到,获得积分10
6秒前
吴博文完成签到,获得积分10
7秒前
一滴水的沙漠关注了科研通微信公众号
7秒前
大白完成签到,获得积分10
7秒前
7秒前
夹心完成签到,获得积分10
8秒前
8秒前
8秒前
王伊辰完成签到,获得积分10
8秒前
wd123发布了新的文献求助30
9秒前
10秒前
10秒前
10秒前
乐辰发布了新的文献求助10
10秒前
tian关注了科研通微信公众号
10秒前
euphoria完成签到,获得积分10
10秒前
Criminology34应助双显卡采纳,获得30
10秒前
Hello应助契心采纳,获得10
11秒前
高分求助中
Encyclopedia of Quaternary Science Third edition 2025 12000
(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
HIGH DYNAMIC RANGE CMOS IMAGE SENSORS FOR LOW LIGHT APPLICATIONS 1500
Constitutional and Administrative Law 1000
The Social Work Ethics Casebook: Cases and Commentary (revised 2nd ed.). Frederic G. Reamer 800
Holistic Discourse Analysis 600
Vertébrés continentaux du Crétacé supérieur de Provence (Sud-Est de la France) 600
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 5349030
求助须知:如何正确求助?哪些是违规求助? 4483063
关于积分的说明 13953616
捐赠科研通 4381885
什么是DOI,文献DOI怎么找? 2407617
邀请新用户注册赠送积分活动 1400303
关于科研通互助平台的介绍 1373471