热泳
聚苯乙烯
温度梯度
粒子(生态学)
化学物理
微尺度热泳
密闭空间
化学工程
材料科学
微流控
粒径
化学
聚合物
热力学
纳米技术
纳米颗粒
物理化学
复合材料
有机化学
纳米流体
工程类
生物化学
海洋学
物理
量子力学
地质学
作者
Haolan Xu,Xu Zheng,Xinghua Shi
标识
DOI:10.1016/j.jcis.2023.01.112
摘要
Particle transport by a temperature gradient is prospective in many biomedical applications. However, the prevalence of boundary confinement in practical use introduces synergistic effects of thermophoresis and thermo-osmosis, causing controversial phenomena and great difficulty in understanding the mechanisms.We developed a microfluidic chip with a uniform temperature gradient and switchable substrate hydrophilicity to measure the migrations of various particles (d = 200 nm - 2 μm), through which the effects of particle thermophoresis and thermo-osmotic flow from the substrate surface were decoupled. The contribution of substrate hydrophilicity on thermo-osmosis was examined. Thermophoresis was measured to clarify its dependence on particle size and hydrophilicity.This paper reports the first experimental evidence of a large enthalpy-dependent thermo-osmotic mobility χ ∼ ΔH on a hydrophobic polymer surface, which is 1-2 orders of magnitude larger than that on hydrophilic surfaces. The normalized Soret coefficient for polystyrene particles, ST/d = 18.0 K-1µm-1, is confirmed to be constant, which helps clarify the controversy of the size dependence. Besides, the Soret coefficient of hydrophobic proteins is approximately-four times larger than that of hydrophilic extracellular vesicles. These findings suggest that the intrinsic slip on the hydrophobic surface could enhance both surface thermo-osmosis and particle thermophoresis.
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