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AM Howe

Publications and source records attributed to AM Howe.

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Small-Angle Neutron Scattering and Fluorescence Studies of Mixed Surfactants with Dodecyl Tails.

The mixed micelles formed in solutions of the anionic surfactant sodium dodecylsulfate (SDS) and the nonionic surfactant dodecylmalono-bis-N-methylglucamide (DBNMG) were studied by surface tension, fluorescence, and small-angle neutron scattering. Measurements of the critical micelle concentration (CMC) by surface tension and fluorescence show that these two surfactants mix nonideally. The experimental values of the CMCs for surfactant mixtures for all compositions are less than the ideal prediction proposed by Clint (J. Chem. Soc. 71, 1327 (1975)). Regular solution theory (for example, Penfold et al., Langmuir 11, 2498 (1995)) can be used to calculate the composition of the micelle at the CMC. The micellar composition thus calculated differs significantly from that at higher total surfactant concentrations, the latter being much closer to the stoichiometric composition. The polarity of the micellar environment, as perceived by a solubilized fluorescence probe, is identical for both the single-component and the mixed micelles. The scattering data show that the mixed micelles are comparable in size to the pure nonionic micelle and slightly larger than the anionic micelle. Parallel studies with deuterated SDS showed no evidence of segregation or local ordering within the mixed micelle. The effective charge on the mixed micelle is determined by the amount of ionic surfactant within the micelle. Addition of 0.1 M NaCl to these systems has no effect on the CMC, micelle ellipticity, and aggregation number-a behavior very different from that observed for simple SDS solutions. Copyright 1999 Academic Press.

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Study of a Solvated Adsorbed Gelatin Layer Using a Modified Force Microscope.

The interaction energies between gelatin-coated surfaces at various electrolyte and pH conditions are reported. The surfaces are of glass and are negatively charged under all conditions used here. Gelatin is a polyampholyte, with an isoelectric pH (IEP) of approximately 4.9. At low pH the gelatin molecules have a net positive charge, and thus the polyampholyte tends to adsorb with a relatively flat conformation. As the pH is increased the strong attractive interaction between the surface and the polyampholyte decreases as more negative charges and then fewer positive charges appear on the polyampholyte, and so the gelatin extends away from the surface. On changing electrolyte concentrations after adsorption no effect was seen at the IEP, but the layer was observed to swell at more alkaline pHs. This is consistent with the net minimum charge situation on the polymer under these conditions. Changing the adsorption conditions was seen to have an effect, and this is attributed to the different affinities of the gelatin chain to the surface depending on the solution chemistry. Results obtained when the gelatin was initially adsorbed on one surface or two were similar, suggesting that the gelatin transfers rapidly from one surface to another. The importance of adsorption conditions as well as current conditions is discussed. Copyright 1999 Academic Press.

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