论文标题
在微通道突然膨胀时,涂层的微螺旋体的自组装
Self-assembly of coated microdroplets at the sudden expansion of a microchannel
论文作者
论文摘要
我们报告了在微流体通道突然膨胀的情况下,对涂层液滴的自组装观察到了常规簇。通过在通道膨胀的上游创建了由常规涂层微螺旋杆组成的双重乳液,从而通过施加不同的入口压力来改变漏斗距离,液滴长度,速度和涂层厚度,尽管不是独立的。只要放大的通道仍然足够局限于禁止在双文件中传播,液滴可以在扩展时顺序组装成常规的线性簇。液滴通过其涂料膜的合并与前方的群体结合。当液滴在膨胀处相互接近临界距离之内时,这种聚结会发生,这是由于火车内的流体动力相互作用而实现的。由于合并过程中液滴组件的重新配置会增加与以下液滴的距离,因此获得了包含有限数量的液滴的簇。减小滴滴距离将群集的大小提高到最大值,超出了连续簇形成的最大值。在一个简单的模型中正式化这些观察结果表明,任何大小的簇都是可能的,但是它们是出于越来越狭窄的参数值范围而发生的。我们的实验观察结果表明,背景实验波动限制了实践中最大离散群集的大小。这种自组装方法为将多个核心封装在单个涂层膜中的流动聚焦提供了一种强大的替代方法,并有可能通过减少簇来构建更复杂的胶体构建块。
We report observations of the self-assembly of coated droplets into regular clusters at the sudden expansion of a microfluidic channel. A double emulsion consisting of a regular train of coated microdroplets was created upstream of the channel expansion, so that the inter-drop distance, droplet length, velocity and coating thickness could be varied by imposing different inlet pressures, albeit not independently. Provided that the enlarged channel remains sufficiently confined to prohibit propagation in double file, droplets can assemble sequentially into regular linear clusters at the expansion. Droplets join a cluster via the coalescence of their coating film with that of the group ahead. This coalescence occurs when the droplets approach each other to within a critical distance at the expansion, enabled by hydrodynamic interactions within the train. Clusters comprising a finite number of droplets are obtained because reconfiguration of the droplet assembly during coalescence increases the distance to the following droplet. Decreasing the inter-drop distance increases the cluster size up to a maximum value beyond which continuous clusters form. Formalising these observations in a simple model reveals that clusters of any size are possible but that they occur for increasingly narrow ranges of parameter values. Our experimental observations suggests that background experimental fluctuations limit the maximum discrete cluster size in practice. This method of self-assembly offers a robust alternative to flow focusing for encapsulating multiple cores in a single coating film and the potential to build more complex colloidal building blocks by de-confining the clusters.