Electrodynamic tailoring of self-assembled three-dimensional electrospun constructs

材料科学 极化(电化学) 纳米技术 电场 静电学 喷嘴 聚合物 化学物理 复合材料 原位 纤维 自组装 静电纺丝 机械工程 化学 物理 有机化学 物理化学 量子力学 工程类
作者
Tiago Marques dos Reis,Ilídio J. Correia,Ana Aguiar‐Ricardo
出处
期刊:Nanoscale [The Royal Society of Chemistry]
卷期号:5 (16): 7528-7528 被引量:22
标识
DOI:10.1039/c3nr01668d
摘要

The rational design of three-dimensional electrospun constructs (3DECs) can lead to striking topographies and tailored shapes of electrospun materials. This new generation of materials is suppressing some of the current limitations of the usual 2D non-woven electrospun fiber mats, such as small pore sizes or only flat shaped constructs. Herein, we pursued an explanation for the self-assembly of 3DECs based on electrodynamic simulations and experimental validation. We concluded that the self-assembly process is driven by the establishment of attractive electrostatic forces between the positively charged aerial fibers and the already collected ones, which tend to acquire a negatively charged network oriented towards the nozzle. The in situ polarization degree is strengthened by higher amounts of clustered fibers, and therefore the initial high density fibrous regions are the preliminary motifs for the self-assembly mechanism. As such regions increase their in situ polarization electrostatic repulsive forces will appear, favoring a competitive growth of these self-assembled fibrous clusters. Highly polarized regions will evidence higher distances between consecutive micro-assembled fibers (MAFs). Different processing parameters--deposition time, electric field intensity, concentration of polymer solution, environmental temperature and relative humidity--were evaluated in an attempt to control material's design.

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
jcz关闭了jcz文献求助
刚刚
科研通AI6.3应助hezwy采纳,获得10
刚刚
彭彭发布了新的文献求助10
1秒前
3秒前
4秒前
4秒前
liao举报开朗的lala求助涉嫌违规
4秒前
5秒前
7秒前
7秒前
sun发布了新的文献求助10
8秒前
Jerryhuw发布了新的文献求助10
8秒前
9秒前
Cathy发布了新的文献求助10
9秒前
9秒前
傅梦槐发布了新的文献求助20
10秒前
10秒前
11秒前
沈济舟发布了新的文献求助10
12秒前
李爱国应助susu1616采纳,获得20
14秒前
夏文钦发布了新的文献求助30
14秒前
CipherSage应助徐笑松采纳,获得10
15秒前
birdy完成签到,获得积分10
15秒前
初阳发布了新的文献求助10
15秒前
苗条故事发布了新的文献求助10
15秒前
15秒前
科研通AI6.2应助温可可采纳,获得10
15秒前
16秒前
16秒前
杨华启应助子辰采纳,获得10
16秒前
19秒前
含糊的钢笔完成签到,获得积分20
20秒前
HOLDMEN完成签到 ,获得积分10
21秒前
夏文钦完成签到,获得积分10
23秒前
24秒前
25秒前
25秒前
25秒前
26秒前
所所应助Juujuucc采纳,获得20
27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
Modern Epidemiology, Fourth Edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Social Cognition: Understanding People and Events 800
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6026593
求助须知:如何正确求助?哪些是违规求助? 7670703
关于积分的说明 16183288
捐赠科研通 5174539
什么是DOI,文献DOI怎么找? 2768806
邀请新用户注册赠送积分活动 1752171
关于科研通互助平台的介绍 1638066