Differential behavior of sodium laurylsulfate micelles in the presence of nonionic polymers

Chandra Ade-Browne, Arnab Dawn, Marzieh Mirzamani, Shuo Qian, Harshita Kumari

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Hypothesis: Theory and practice have proven that the cleansing properties and irritation potential of surfactants can be controlled with the addition of co-surfactants or polymers. The size of the surfactant-polymer nanoassembly, which differs from the pure surfactant micelle, has been postulated to be the cause of the differences in a surfactant system's ability to disrupt the skin barrier. However, a firm structure–function relationship connecting polymer and surfactant under a consumer relevant condition is yet to be established. It is therefore hypothesized that apart from the size, the shape and the chemical nature of the polymer might play crucial roles. Experiments: We used combined small-angle neutron scattering, nuclear magnetic resonance spectroscopy, tensiometry, and dye solubilization methods to investigate the shape, size, and intermolecular interactions involved in sodium laurylsulfate-based systems in the presence of two industrially important and chemically distinct polymers, polyethylene glycol and polyvinyl alcohol, adopting a consumer relevant protocol. Findings: Apart from size, shape and inter-micellar interactions fine-tuned by the presence of the polymers are found to be the important factors. Secondly, the physicochemical property of the polymer including chemical structure, conformation, hydrophilicity, presence of side groups, all can have crucial influence on polymer-surfactant interaction, micelle formation, and micelle stability.

Original languageEnglish
Pages (from-to)276-283
Number of pages8
JournalJournal of Colloid and Interface Science
Volume544
DOIs
StatePublished - May 15 2019

Funding

We would like to acknowledge Dr. Mike Weaver, Ryan Thompson, and Dr. Robert Glenn from P&G, Dr. Chris Garvey (ANSTO), Dr. Boualem Hammouda (NIST), Dr. Kavssery Ananthapadmanabhan (UC) and Dr. Vinod Aswal (BARC) for valuable discussions. This work benefited from the use of the SasView application, originally developed under NSF award DMR-0520547 . SasView contains code developed with funding from the European Union's Horizon 2020 research and innovation programme under the SINE2020 project, grant agreement No 654000 . The High Flux Isotope Reactor, where Bio-SANS is located, are supported by US Department of Energy Office of Science User Facility. The Bio-SANS of the Center for Structural Molecular Biology is supported by the Office of Biological and Environmental Research of the US Department of Energy. This work was primarily supported by start-up funds from UC (HK) and partially supported by the Procter and Gamble Company (Cincinnati, OH). We would like to acknowledge Dr. Mike Weaver, Ryan Thompson, and Dr. Robert Glenn from P&G, Dr. Chris Garvey (ANSTO), Dr. Boualem Hammouda (NIST), Dr. Kavssery Ananthapadmanabhan (UC) and Dr. Vinod Aswal (BARC) for valuable discussions. This work benefited from the use of the SasView application, originally developed under NSF award DMR-0520547. SasView contains code developed with funding from the European Union's Horizon 2020 research and innovation programme under the SINE2020 project, grant agreement No 654000. The High Flux Isotope Reactor, where Bio-SANS is located, are supported by US Department of Energy Office of Science User Facility. The Bio-SANS of the Center for Structural Molecular Biology is supported by the Office of Biological and Environmental Research of the US Department of Energy.

FundersFunder number
Procter and Gamble Company (Cincinnati, OH)
National Science FoundationDMR-0520547
U.S. Department of Energy
University of California
Biological and Environmental Research
Horizon 2020 Framework Programme
Horizon 2020654000
National Science Foundation

    Keywords

    • Micelle
    • Polymer
    • Polymer–surfactant interaction
    • Self-assembly
    • Small-angle neutron scattering

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