Rheology of silica dispersions in organic liquids: New evidence for solvation forces dictated by hydrogen bonding

被引:401
作者
Raghavan, SR
Walls, HJ
Khan, SA [1 ]
机构
[1] N Carolina State Univ, Dept Chem Engn, Raleigh, NC 27695 USA
[2] Univ Delaware, Dept Chem Engn, Newark, DE 19716 USA
关键词
D O I
10.1021/la991548q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dispersions of hydrophilic fumed silica are investigated in a range of polar organic media. The silica forms stable, low-viscosity sols exhibiting sheer thickening behavior in a host of liquids, including ethylene glycol and its oligomers and short-chain alcohols, such as n-propanol. In contrast, the silica flocculates into colloidal gels in other liquids, such as glycols with methyl end-caps and longer-chain alcohols. We suggest that there is a causal relationship between the hydrogen-bonding ability of the liquid and the colloidal microstructure observed. In strongly hydrogen-bonding Liquids, a solvation layer is envisioned to form on the silica surface through hydrogen bonding between liquid molecules and surface silanol groups (Si-OH). This gives rise to short-range, non-DLVO repulsions ("solvation forces") which stabilize the silica particles. In contrast, in the case of liquids with Limited hydrogen-bonding ability, silanols on adjacent silica particles are envisioned to interact directly by hydrogen banding. This leads to particle flocculation and ultimately to gelation. Our study further fuels the debate regarding the existence of solvation forces in dispersions.
引用
收藏
页码:7920 / 7930
页数:11
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