Polyvinylidene Fluoride (PVDF) Crystallization Kinetics in an Electric Field

结晶 聚偏氟乙烯 电场 材料科学 聚合物 动力学 活化能 化学工程 复合材料 分析化学(期刊) 化学 物理化学 色谱法 物理 量子力学 工程类
作者
Rizmahardian Ashari Kurniawan,Peter P. Chu
出处
期刊:Journal of Macromolecular Science, Part B [Informa]
卷期号:62 (12): 738-754 被引量:1
标识
DOI:10.1080/00222348.2023.2246262
摘要

AbstractTo study the effect of applied electric field on polymer crystallization, the crystallization of polyvinylidene fluoride (PVDF) was observed under modified polarized optical microscopy. The PVDF melts were crystallized based on programmed temperature, changes between two transparent conductive glass electrodes, on which a DC electric field was applied. The observations revealed that without the electric field, crystallizations below 160 °C resulted in only α-form crystals, while, at elevated temperatures, the formation of γ-form crystals also occurred. By applying the electric field at 1.7 kV/cm, γ-form crystals started emerging at the slightly lower temperature of 158 °C. Further examinations showed that both crystals, α-form and γ-form, grew at a greater rate with increasing field strength. A careful calculation of the Avrami parameters supported the data that the electric field enhanced the crystallization kinetics. Careful calculation based on the Laurientz–Hoffmann approach revealed that applying the electric field decreased the required energy for PVDF crystallization. The folding surface free energy of the PVDF crystallization, 1.76 × 10−2 Jm−2, was reduced to 1.57 × 10−2 Jm−2 and 1.43 × 10−2 Jm−2 after applying electric fields of 0.8 and 1.7 kVcm−1, respectively. We suggest that the electric field promoted the polymer chain alignment during the crystallization; as a result, it accelerated the polymer crystallization and lowered the energy requirement for crystallization.Keywords: applied electric fieldisothermal crystallizationkineticspolyvinylidene fluoride Disclosure statementNo potential conflict of interest was reported by the author(s).Additional informationFundingThis study was supported by a grant from the Universitas Muhammadiyah Pontianak (HI-2023).
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
大幅提高文件上传限制,最高150M (2024-4-1)

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
1秒前
2秒前
风格和完成签到,获得积分10
2秒前
orixero应助围城采纳,获得10
3秒前
3秒前
朝朝发布了新的文献求助10
5秒前
手机应助派大星采纳,获得20
6秒前
7秒前
轻松的化蛹完成签到,获得积分10
7秒前
发疯的游子完成签到 ,获得积分10
8秒前
Quinta发布了新的文献求助10
8秒前
8秒前
bkagyin应助科研通管家采纳,获得20
8秒前
小二郎应助科研通管家采纳,获得10
8秒前
充电宝应助科研通管家采纳,获得10
8秒前
dongsheng应助科研通管家采纳,获得10
8秒前
昏睡的绍辉完成签到,获得积分10
8秒前
隐形曼青应助科研通管家采纳,获得10
8秒前
9秒前
林巧完成签到 ,获得积分10
9秒前
CipherSage应助dnicly采纳,获得10
9秒前
可爱的函函应助dnicly采纳,获得10
9秒前
wangyy65发布了新的文献求助10
10秒前
淡淡菠萝发布了新的文献求助10
10秒前
13秒前
14秒前
科研通AI2S应助XHT采纳,获得10
14秒前
17秒前
Cecilia完成签到,获得积分10
17秒前
yar完成签到,获得积分0
19秒前
天气真好发布了新的文献求助10
20秒前
21秒前
21秒前
Quinta完成签到,获得积分10
23秒前
re发布了新的文献求助10
24秒前
24秒前
sugar完成签到,获得积分10
25秒前
25秒前
景清完成签到,获得积分10
29秒前
似水无痕完成签到,获得积分10
30秒前
高分求助中
Mantiden: Faszinierende Lauerjäger Faszinierende Lauerjäger Heßler, Claudia, Rud 1000
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 1000
Natural History of Mantodea 螳螂的自然史 1000
A Photographic Guide to Mantis of China 常见螳螂野外识别手册 800
Autoregulatory progressive resistance exercise: linear versus a velocity-based flexible model 500
Spatial Political Economy: Uneven Development and the Production of Nature in Chile 400
Research on managing groups and teams 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3329457
求助须知:如何正确求助?哪些是违规求助? 2959146
关于积分的说明 8594359
捐赠科研通 2637590
什么是DOI,文献DOI怎么找? 1443651
科研通“疑难数据库(出版商)”最低求助积分说明 668775
邀请新用户注册赠送积分活动 656220