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Adsorption of surface functionalized silica nanoparticles onto mineral surfaces and decane/water interface

机译:表面官能化的二氧化硅纳米粒子在矿物表面和癸烷/水界面上的吸附

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摘要

The adsorption of silica nanoparticles onto representative mineral surfaces and at the decane/water interface was studied. The effects of particle size (the mean diameters from 5 to 75 nm), concentration and surface type on the adsorption were studied in detail. Silica nanoparticles with four different surfaces [unmodified, surface modified with anionic (sulfonate), cationic (quaternary ammonium (quat)) or nonionic (polyethylene glycol (PEG)) surfactant] were used. The zeta potential of these silica nanoparticles ranges from −79.8 to 15.3 mV. The shape of silica particles examined by a Hitachi-S5500 scanning transmission electron microscope (STEM) is quite spherical. The adsorption of all the nanoparticles (unmodified or surface modified) on quartz and calcite surfaces was found to be insignificant. We used interfacial tension (IFT) measurements to investigate the adsorption of silica nanoparticles at the decane/water interface. Unmodified nanoparticles or surface modified ones with sulfonate or quat do not significantly affect the IFT of the decane/water interface. It also does not appear that the particle size or concentration influences the IFT. However, the presence of PEG as a surface modifying material significantly reduces the IFT. The PEG surface modifier alone in an aqueous solution, without the nanoparticles, yields the same IFT reduction for an equivalent PEG concentration as that used for modifying the surface of nanoparticles. Contact angle measurements of a decane droplet on quartz or calcite plate immersed in water (or aqueous nanoparticle dispersion) showed a slight change in the contact angle in the presence of the studied nanoparticles. The results of contact angle measurements are in good agreement with experiments of adsorption of nanoparticles on mineral surfaces or decane/water interface. This study brings new insights into the understanding and modeling of the adsorption of surface-modified silica nanoparticles onto mineral surfaces and water/decane interface.
机译:研究了二氧化硅纳米粒子在代表性矿物表面以及癸烷/水界面的吸附。详细研究了粒径(平均直径为5至75 nm),浓度和表面类型对吸附的影响。使用具有四个不同表面的二氧化硅纳米颗粒[未改性,用阴离子(磺酸盐),阳离子(季铵(季铵))或非离子(聚乙二醇(PEG))表面活性剂改性的表面)。这些二氧化硅纳米粒子的Zeta电位范围为-79.8至15.3 mV。由Hitachi-S5500扫描透射电子显微镜(STEM)检查的二氧化硅颗粒的形状非常球形。发现所有纳米颗粒(未改性或表面改性)在石英和方解石表面上的吸附均微不足道。我们使用界面张力(IFT)测量来研究二氧化硅纳米粒子在癸烷/水界面的吸附。未改性的纳米颗粒或经磺酸或季铵盐改性的纳米颗粒不会显着影响癸烷/水界面的IFT。似乎粒度或浓度也不影响IFT。然而,PEG作为表面改性材料的存在显着降低了IFT。在水溶液中,没有纳米颗粒的情况下,单独的PEG表面改性剂与用于修饰纳米颗粒表面的当量PEG浓度产生相同的IFT降低。浸入水中的石英或方解石板上癸烷液滴的接触角测量结果表明,在存在研究的纳米粒子的情况下,接触角略有变化。接触角的测量结果与纳米颗粒在矿物表面或癸烷/水界面上的吸附实验非常吻合。这项研究为将表面改性的二氧化硅纳米粒子吸附到矿物表面和水/癸烷界面上的理解和建模带来了新的见解。

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