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在聚丙烯酸存在下氧化铝包覆二氧化钛浆料的分散:一价抗衡离子的影响

Dispersion of alumina-coated TiO2 slurries in the presence of poly(acrylic) acid influence of monovalent counterions.

作者信息

Boisvert Jean-Philippe, Malgat Alexandre

机构信息

CIPP, Université du Québec à Trois-Rivières, C.P. 500, Trois-Rivières, Québec G9A5H7, Canada.

出版信息

J Colloid Interface Sci. 2005 Jan 15;281(2):389-97. doi: 10.1016/j.jcis.2004.08.104.

Abstract

The rheological behavior of concentrated alumina-coated TiO2 slurries has been investigated in connection with the type of surface counterions (monovalent cations: X = Li+, Na+, TMA+) in the absence and in the presence of polyacrylic acid (PAA). The study has been conducted in a pH range of 4-10 and with ionic strengths lower than 0.01 M. The pH and ionic strength were adjusted with XOH and XCl, respectively. The surface properties have been investigated by titration of surface counterions and the apparent yield stress has been measured using a dynamic stress rheometer. It appears from the results that the pH at the maximum yield stress and the magnitude of the yield stress depend on the nature of the counterion. The yield stress measurements were also conducted in the presence of PAA (0.5 segment/nm2) adsorbed on the particle surface. In that case, the mineral surface and adsorbed polymer were neutralized with XOH. The results show that the dispersion efficiency depends on the polymer counterion. In general, it is found that the maximum yield stress and the corresponding counterion surface density both follow the sequence TMA+ < Na+ < Li+. The adsorption of PAA apparently amplifies the effects observed with the corresponding cation. An electrostriction effect of the hydration layer at the interface is suggested in order to explain the increasing yield stress as the surface density of Li+ increases. The so-called structure-making/structure-breaking model explains the yield stress reduction with the TMA+ surface density.

摘要

研究了在有无聚丙烯酸(PAA)存在的情况下,浓缩氧化铝包覆二氧化钛浆料的流变行为与表面抗衡离子类型(单价阳离子:X = Li⁺、Na⁺、TMA⁺)之间的关系。该研究在pH值为4 - 10且离子强度低于0.01 M的范围内进行。pH值和离子强度分别用XOH和XCl进行调节。通过滴定表面抗衡离子研究了表面性质,并使用动态应力流变仪测量了表观屈服应力。结果表明,最大屈服应力时的pH值和屈服应力的大小取决于抗衡离子的性质。还在颗粒表面吸附有PAA(0.5链段/纳米²)的情况下进行了屈服应力测量。在这种情况下,用XOH中和矿物表面和吸附的聚合物。结果表明,分散效率取决于聚合物抗衡离子。一般来说,发现最大屈服应力和相应的抗衡离子表面密度都遵循TMA⁺ < Na⁺ < Li⁺的顺序。PAA的吸附明显放大了相应阳离子所观察到的效应。为了解释随着Li⁺表面密度增加屈服应力增大的现象,提出了界面处水化层的电致伸缩效应。所谓的结构形成/结构破坏模型解释了随着TMA⁺表面密度增加屈服应力降低的现象。

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