Affiliations 

  • 1 School of Science, State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, China; ISIS Facility, Rutherford Appleton Laboratory, STFC, Didcot, Oxon OX11 0QX, UK
  • 2 ISIS Facility, Rutherford Appleton Laboratory, STFC, Didcot, Oxon OX11 0QX, UK
  • 3 ISIS Facility, Rutherford Appleton Laboratory, STFC, Didcot, Oxon OX11 0QX, UK; Physical and Theoretical Chemistry Laboratory, Oxford University, South Parks Road, Oxford OX1 3QZ, UK. Electronic address: jeff.penfold@stfc.ac.uk
  • 4 Physical and Theoretical Chemistry Laboratory, Oxford University, South Parks Road, Oxford OX1 3QZ, UK
  • 5 School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 3AF, UK
  • 6 KLK Oleo, SDN BDH, Menara KLK, Muliara Damansara, 47810 Petaling Jaya, Selangor, Malaysia
  • 7 Lonza UK, GB-Blackley, Manchester, Lancs M9 8ES, UK
  • 8 School of Science, State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Qingdao 266580, China. Electronic address: zfyancat@upc.edu.cn
J Colloid Interface Sci, 2019 Sep 05;557:124-134.
PMID: 31518834 DOI: 10.1016/j.jcis.2019.09.016

Abstract

The ester sulfonate anionic surfactants are a potentially valuable class of sustainable surfactants. The micellar growth, associated rheological changes, and the onset of precipitation are important consequences of the addition of electrolyte and especially multi-valent electrolytes in anionic surfactants. Small angle neutron scattering, SANS, has been used to investigate the self-assembly and the impact of different valence electrolytes on the self-assembly of a range of ester sulfonate surfactants with subtly different molecular structures. The results show that in the absence of electrolyte small globular micelles form, and in the presence of NaCl, and AlCl3 relatively modest micellar growth occurs before the onset of precipitation. The micellar growth is more pronounced for the longer unbranched and branched alkyl chain lengths. Whereas changing the headgroup geometry from methyl ester to ethyl ester has in general a less profound impact. The study highlights the importance of relative counterion binding strengths and shows how the surfactant structure affects the counterion binding and hence the micelle structure. The results have important consequences for the response of such surfactants to different operational environments.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.