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Dynamic Light Scattering of Semi-Dilute Hydrophobically Modified Alkali-Soluble Emulsion Solutions with Varying Length of Hydrophobic Alkyl Chains

✍ Scribed by S. Dai; K. C. Tam; R. D. Jenkins


Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
234 KB
Volume
203
Category
Article
ISSN
1022-1352

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✦ Synopsis


Abstract

Dynamic light scattering as well as rheological technique was used to study the semi‐dilute hydrophobically modified alkali‐soluble emulsion (HASE) solutions. The solution viscosity increases dramatically, when the overlap concentration C^*^ is exceeded. Two diffusional modes are evident from the decay time distributions of light scattering and they are related to the hydrodynamic correlation length and the apparent hydrodynamic radius of the HASE clusters. The hydrodynamic correlation lengths, as determined from the fast diffusion mode decrease in proportion to the polymer concentrations but increase with increasing the hydrophobicity of the hydrophobes of the macromonomers. The apparent hydrodynamic radii of the clusters, as determined from the slow diffusion mode, increase with increasing polymer concentrations. When the carbon number of the hydrophobes is increased from C~1~ to C~8~, both the viscosities and diffusion coefficients of the slow mode remain almost unchanged. However, they are strongly dependent on the carbon chain length when the carbon number exceeds C~12~, especially for the polymer with C~20~ alkyl chains. The solution viscosities decrease and diffusion coefficients of the slow mode increase with increasing temperatures, however, the parameters of /T remain constant.
Comparison of microstructures of semi‐dilute HASE solutions with (a) short hydrophobic alkyl groups and (b) long hydrophobic alkyl groups was made. For (a) with small hydrophobes, the aggregation number per association junction is smaller and there are more aggregation junctions in the network cluster. The hydrodynamic correlation length, ξ~h~, which is the averaged distance between two aggregation junctions, is shorter. As for (b) with larger hydrophobes, the aggregation number is larger with fewer aggregation junctions in the network cluster. The hydrodynamic correlation length is longer.

magnified imageComparison of microstructures of semi‐dilute HASE solutions with (a) short hydrophobic alkyl groups and (b) long hydrophobic alkyl groups was made. For (a) with small hydrophobes, the aggregation number per association junction is smaller and there are more aggregation junctions in the network cluster. The hydrodynamic correlation length, ξ~h~, which is the averaged distance between two aggregation junctions, is shorter. As for (b) with larger hydrophobes, the aggregation number is larger with fewer aggregation junctions in the network cluster. The hydrodynamic correlation length is longer.