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Electrosteric Repulsion Induced by Superplasticizers between Cement Particles -An Overlooked Mechanism?

机译:高效减水剂在水泥颗粒之间引起的电立体排斥-一个被忽视的机理?

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Dispersion mechanisms of superplasticizers have received much attention over the past years. Recent developments have brought very efficient superplasticizers where the dominant stabilizing mechanism is thought to be via steric repulsion. These new superplasticizers contain an adsorbing backbone onto which non adsorbing side chains are grafted with the objective of getting them to stretch out into the solution from the cement particle surface and induce the steric repulsin upon approach of other particles. Another feature of these polymers is that they induce only very small zeta potentials. Calculations of interaction energies indicate that these polymers act predominantly through steric repulsion. However, the same calculations could lead to the conclusion that all polymers can only act through steric repulsion. The calculation of the steric and electrostatic contributions are greatly dependent on the polymer adsorption conformation and the distribution of charge at the particle surface associated with these adsorbed polyelectrolytes. Many of the assumptions made in calculating interparticle forces are not necessarily good approximations for polyelectrolytes. This paper discusses the limits of the approximations currently used in such calculations and presents a more accurate model for the calculation of these forces. The main result, applicable for a wide range of superplasticizers, is that both electrostatic and steric repulsions should be taken into account, provided the electrostatic charge can be assumed to lie at the outer-bound of the adsorbed layer of superplasticizers. Such information is of primary importance for understanding and solving cement and superplasticizer incompatibilities, as well as for developing novel products.
机译:在过去的几年中,高效减水剂的分散机理受到了广泛的关注。最近的发展带来了非常高效的高效减水剂,其中主要的稳定机理被认为是通过空间排斥。这些新型的高效减水剂含有一个吸附主链,在该主链上接枝了非吸附性侧链,目的是使它们从水泥颗粒表面伸入溶液中,并在接近其他颗粒时引发空间排斥反应。这些聚合物的另一个特征是它们仅诱导非常小的ζ电位。相互作用能的计算表明,这些聚合物主要通过空间排斥作用。但是,相同的计算可能得出以下结论:所有聚合物只能通过空间排斥作用。空间和静电贡献的计算很大程度上取决于聚合物的吸附构象以及与这些吸附的聚电解质相关的颗粒表面电荷的分布。计算粒子间力时所做的许多假设不一定是聚电解质的良好近似值。本文讨论了目前在此类计算中使用的近似值的极限,并提出了一种用于计算这些力的更准确的模型。适用于各种高效减水剂的主要结果是,只要可以假定静电荷位于高效减水剂吸附层的外边界,就应同时考虑静电排斥和空间排斥。这些信息对于理解和解决水泥与高效减水剂的不相容性以及开发新产品至关重要。

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