各种化学性质的疏水氧化物对泡沫的稳定作用

N. G. Vilkova, S. Mishina, E. D. Deputatov
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引用次数: 0

摘要

研究了疏水氧化钛和二氧化硅稳定泡沫的性能。结果表明,当二氧化硅悬浮液中加入六胺(添加量≥10 mmol/l)时,氢指数值对应于碱性区。随着己胺浓度的增加和相对疏水程度的增加,泡沫的稳定性提高到ng = 2.75 mmol/g。然而,当达到一定程度的疏水作用时(例如,悬浮颗粒中的ng≥3),分散系统可能会迅速破坏,这是由于初始悬浮颗粒聚集造成的。给出了这些分散体系的寿命与氢指数(pH)的关系。在pH值为5时形成最稳定的分散体系,接近氧化物的等电点。由20%氧化钛+ 76.6 mmol/l己胺组成的悬浮液获得的泡沫在pH = 5时保持稳定4天或更长时间,表面的相对疏水性(ng)从0.383变化到1.27 mmol/g。当表面疏水程度显著增加到4.6 mmol/g,且pH值相同时,发泡不明显(层高(h)为0.2 cm),寿命t≈10秒。可能只有达到一定疏水程度时,颗粒才会在液气界面上固定,这是一个不可逆的过程。为了解释由pH值引起的含二氧化钛泡沫稳定性变化的可能原因,我们用沉降分析的方法研究了颗粒大小的分布。结果表明,在pH=10时,平均半径为3µm的悬浮液的分数组成为50%,同时最大半径为21µm;颗粒的润湿角为40.8º。在酸性介质(pH=2-3)和pH=5时,平均颗粒半径为5µm的馏分含量分别为29%和30%。然而,在pH=2时,较低的润湿角值(14.7º)会导致泡沫在酸性环境中的稳定性较低。通过改变疏水氧化钛悬浮液中分散介质的粘度,获得了高度稳定的泡沫。在9.0%二氧化钛+ 0.7%己胺(pH=9)的悬浮液中加入甘油,得到凝胶泡沫,10天内未破坏。然而,在加入等量甘油的酸性介质中,没有观察到形成稳定的分散体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FOAMS STABILIZATION BY HYDROPHOBIZED OXIDES OF VARIOUS CHEMICAL NATURE
The properties of foams stabilized by hydrophobized titanium oxide and silica are studied. It was shown that when hexylamine was added to silica suspensions (in an amount of ≥ 10 mmol/l), the values of the hydrogen index corresponded to the alkaline region. Moreover, the stability of such foams increases with the increasing concentration of hexylamine and an increase in the relative degree of hydrophobization to ng = 2.75 mmol/g. However, rapid destruction of disperse systems is possible when a certain degree of hydrophobization is achieved (for example, ng≥3 in aerosil suspensions), which is due to aggregation of particles in the initial suspension. The dependence of the lifetime of these dispersed systems on the hydrogen index (pH) is shown. The most stable disperse systems were formed at the pH value of 5, which is close to the isoelectric point of the oxide. Foams obtained from the suspension of the composition: 20% titanium oxide + 76.6 mmol/l hexylamine remained stable for four days or more at pH = 5 and a change in the relative hydrophobicity of the surface (ng) from 0.383 to 1.27 mmol/g. With a significant increase in the degree of hydrophobization of the surface to 4.6 mmol/g and the same pH value, foaming was insignificant (the layer height (h) was 0.2 cm) and life time t≈10 sec.  Probably fixing the particles at the liquid-gas interface is an irreversible process only when a certain degree of hydrophobicity is achieved. To explain the possible causes of change stability of the foam containing the titanium dioxide from the pH we have investigated the distribution of particles according to their sizes by the method of sedimentation analysis. It was found that at pH=10 the fractional composition of the suspension with an average radius of 3 µm was equal to 50%, at the same time the maximum radius was 21 µm; the value of the wetting angle of the particles was equal to 40.8º. In an acidic medium (pH=2-3) and at pH=5, the fraction content with an average particle radius of 5 µm was 29% and 30%, respectively. However, low (14.7º) values of the wetting angle at pH=2 can cause low stability of foams in an acidic environment. Highly stable foams were obtained by changing the viscosity of the dispersion medium in suspensions of hydrophobized titanium oxide. When adding glycerol to the suspension composition: 9.0% titanium dioxide + 0.7% hexylamine, pH=9, gel foam was obtained, which was not destroyed within 10 days. However, in an acidic medium with the addition of the same amount of glycerol, the formation of a stable dispersed system was not observed.
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