Dielectric spectroscopic and molecular simulation evidence for aggregation of surfactant-stabilized calcium carbonate nanocolloids in organic media

被引:25
作者
Bearchell, CA
Edgar, JA
Heyes, DM
Taylor, SE
机构
[1] Univ Surrey, Dept Chem, Guildford GU2 5XH, Surrey, England
[2] BP Oil, Sunbury TW16 7LN, Middx, England
关键词
dielectric spectroscopy; calcium carbonate nanocolloids; overbased detergents; molecular simulations;
D O I
10.1006/jcis.1998.5945
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dielectric spectroscopy carried out on overbased phenate micelle particles of nominal diameter similar to 2 mm containing calcium carbonate cores in hydrophobic liquids indicates that the micelles are strongly aggregated. Mean cluster sizes in excess of similar to 10(3) individual micelles are typically found in toluene, The level of association is a little higher in dodecane which is chemically closer to engine oil, the usual solvent for these systems. The mean aggregate size increases dramatically with concentration above an effective solids volume fraction of similar to 0.1 on treating the micelles as spheres. Aggregate size also depends on the level of overbasing, with lower levels of overbasing giving more micelles in the cluster, Molecular dynamics simulations of individual micelle particles reveal them to have large dipole moments originating mainly from the amorphous carbonate cores. Dipoles of magnitude similar to 20D are typical for a range of different surfactant types used in the model. The magnitude of the dipole depends somewhat on the chemical composition of the stabilizing surfactant shell. Monte Carlo simulations of two phenate nanocolloids taking into account all atom and charge pair interactions show these particles to have a strong short-range coulombic attraction of typically -25k(B)T at T = 298 K in the favored "side-by-side" relative arrangement. This attraction could be responsible for the strong level of association inferred from the dielectric spectroscopy experiments. (C) 1999 Academic Press.
引用
收藏
页码:231 / 240
页数:10
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