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基于烃基功能化纳米粒子的尺寸和形态依赖性表面润湿性。

Size and morphology dependent surface wetting based on hydrocarbon functionalized nanoparticles.

机构信息

Energy Safety Research Institute (ESRI), Swansea University Bay Campus, Fabian Way, Swansea SA1 8EN, UK.

Centre for Water Advanced Technologies and Environmental Research (CWATER), College of Engineering, Swansea University, Fabian Way, Swansea SA1 8EN, UK; Environmental Engineering Department, Al-Mustansiriya University, Iraq.

出版信息

J Colloid Interface Sci. 2019 May 1;543:328-334. doi: 10.1016/j.jcis.2019.02.058. Epub 2019 Feb 20.

Abstract

HYPOTHESIS

The wetting properties of films created using metal oxide nanoparticles can be controlled through roughness and chemical functionality; however, other variations such as the size and shape of the particles play an important role in improved understanding of the wetting behaviour of these materials.

EXPERIMENTS

Infrared (IR) spectroscopy and thermogravimetric analysis (TGA) were used to study the chemisorption and grafting density of a carboxylic acid onto the surface of nanoparticles. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) were used to investigate the morphology and roughness of the nanoparticle films. To investigate the wettability and surface energy of the films, static and dynamic contact angle (CA) measurements were used.

FINDINGS

Smaller, spherical nanoparticles (<50 nm) were observed to create films that displayed greater surface roughness and showed superhydrophobic properties. By comparison, larger, 135 nm spherical nanoparticles showed reduced surface roughness and displayed water contact angles (WCAs) <150°. Since these particles showed similar carboxylate grafting densities, this suggests that there is a particle size limit above which it is not possible to deposit superhydrophobic films. This study also shows that topographical effects brought about by film roughness can be overcome through increasing the carboxylate grafting density on the surface of the nanoparticles. It was observed that films created using mix shape <50 nm nanoparticles with relatively low surface roughness displayed superhydrophobic WCAs and low hysteresis. These particles also possessed a substantially larger carboxylate grafting density, indicating that the extent of functionalization also has a large bearing on the wettability of the films. Herein, we show that particle size, morphology, and reactivity all play important roles in determining the wettability of nanoparticle films.

摘要

假设

通过控制薄膜的粗糙度和化学官能团,可以控制使用金属氧化物纳米粒子制造的薄膜的润湿性;然而,颗粒的其他变化,如颗粒的大小和形状,对于更好地理解这些材料的润湿性行为也起着重要作用。

实验

采用红外(IR)光谱和热重分析(TGA)研究羧酸在纳米粒子表面的化学吸附和接枝密度。扫描电子显微镜(SEM)和原子力显微镜(AFM)用于研究纳米粒子薄膜的形貌和粗糙度。为了研究薄膜的润湿性和表面能,使用静态和动态接触角(CA)测量。

结果

观察到较小的、球形的纳米粒子(<50nm)形成的薄膜具有更大的表面粗糙度,并表现出超疏水性。相比之下,较大的、135nm 的球形纳米粒子显示出较低的表面粗糙度,并表现出小于 150°的水接触角(WCA)。由于这些颗粒显示出相似的羧酸盐接枝密度,这表明存在一个颗粒尺寸限制,超过该限制就不可能沉积超疏水性薄膜。本研究还表明,通过增加纳米粒子表面的羧酸盐接枝密度,可以克服由薄膜粗糙度带来的形貌效应。观察到使用混合形状<50nm 纳米粒子形成的薄膜具有相对较低的表面粗糙度,显示出超疏水性 WCA 和低滞后性。这些颗粒还具有较大的羧酸盐接枝密度,表明官能化程度也对薄膜的润湿性有很大影响。在这里,我们表明颗粒大小、形态和反应性都在决定纳米粒子薄膜的润湿性方面起着重要作用。

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