Mineral Processing R&D, Cytec Industries Inc., Stamford, Connecticut 06902, USA.
Nat Mater. 2010 May;9(5):436-41. doi: 10.1038/nmat2724. Epub 2010 Mar 21.
Self-assembly of surfactant molecules into micelles of various shapes and forms has been extensively used to synthesize soft nanomaterials. Translucent solutions containing rod-like surfactant micelles can self-organize under flow to form viscoelastic gels. This flow-induced structure (FIS) formation has excited much fundamental research and pragmatic interest as a cost-effective manufacturing route for active nanomaterials. However, its practical impact has been very limited because all reported FIS transitions are reversible because the gel disintegrates soon after flow stoppage. We present a new microfluidics-assisted robust laminar-flow process, which allows for the generation of extension rates many orders of magnitude greater than is realizable in conventional devices, to produce purely flow-induced permanent nanogels. Cryogenic transmission electron microscopy imaging of the gel reveals a partially aligned micelle network. The critical flow rate for gel formation is consistent with the Turner-Cates fusion mechanism, proposed originally to explain reversible FIS formation in rod-like micelle solutions.
表面活性剂分子自组装成各种形状和形式的胶束,已被广泛用于合成软纳 米材料。含有棒状表面活性剂胶束的半透明溶液在流动下可以自组织形成粘弹 性凝胶。这种流动诱导结构(FIS)的形成激发了大量的基础研究和实际应用兴 趣,因为它是一种具有成本效益的活性纳米材料制造途径。然而,由于所有报 告的 FIS 转变都是可逆的,因为凝胶在停止流动后很快就会分解,因此其实际 影响非常有限。我们提出了一种新的微流辅助稳定层流工艺,该工艺可以产生 比传统设备可实现的大几个数量级的拉伸率,从而产生纯流动诱导的永久性纳 米凝胶。凝胶的低温传输电子显微镜成像显示出部分对齐的胶束网络。形成凝 胶的临界流速与最初用于解释棒状胶束溶液中可逆 FIS 形成的特纳-凯茨融合机 制一致。