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J Samseth

Publications and source records attributed to J Samseth.

3 recordsLinked to original sources

Interfacial Modification as a Route to Novel Bilayered Morphologies in Binary Block Copolymer/Homopolymer Blends.

Addition of a relatively low-molecular-weight parent homopolymer to a lamellar AB diblock copolymer constitutes a reliable means by which to induce, in controllable fashion, transitions to other morphologies. In this study, we examine the effect of interfacial modification on such transitions in "extended" A(A/B)B copolymer/homopolymer blends in which (i) the A/B midblock fraction (relative to the copolymer molecular weight) is varied from 0.0 to 0.4 in 0.1 increments and (ii) the overall concentration of A ranges from 0.50 to 0.95. As this A/B fraction is increased at constant blend composition, the extent of homopolymer-induced lamellar swelling becomes measurably less pronounced, indicating that the A/B midblock serves to delocalize repulsion along the interphase separating adjacent lamellae. At higher homopolymer concentrations, an increase in the A/B fraction results in the formation of either unilamellar vesicles or a randomly connected bilayered membrane, rather than micelles. These membranes become unstable and transform to micelles at high copolymer dilution. The results presented here are discussed in terms of the complex morphologies observed in, and predicted for, low-molar-mass (co)surfactant systems.

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Influence of Alcohol on the Behavior of Sodium Dodecylsulfate Micelles.

The effect of medium chain alcohol molecules on the size and shape of sodium dodecylsulfate micelles, and on the self-diffusion coefficient of the surfactant and alcohol, has been investigated by means of small angle neutron scattering (SANS), and Fourier transform pulsed field gradient spin echo (FT-PGSE) nuclear magnetic resonance measurements. All measurements were done in D2O containing a sodium chloride concentration of 0.4 mol/kg, and a surfactant concentration of 0.04 mol/kg. The alcohols used were 1-propanol, 1-butanol, and 1-pentanol. The data obtained from the different techniques agrees qualitatively. The results show that propanol successively breaks down the micelles while pentanol brings about a structural change toward large wormlike aggregates. Butanol shows a highly complex behavior on the structure of the micelles and can decrease and increase the size of the aggregates, depending on the added alcohol concentration range. All analyzed solutions show a distribution of the alcohol between the aqueous bulk solution and the palisade layer of the micelles, resulting in an increased "hydration" of D2O in the micellar surface. Moreover, the structural changes of the micelles indicate that butanol and pentanol solubilize in the micellar core in the high molality range, near the end of the solubility limit. Propanol is apparently too hydrophilic to do so. Copyright 1998 Academic Press.

Journal Article↗