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Effect of Surfactant Concentration and Hydrophobicity on the Ordering of Water at a Silica Surface.
Shi, Lirong; McMillan, Janet R; Yu, Decai; Chen, Xiaoyun; Tucker, Christopher J; Wasserman, Eric; Mohler, Carol; Chen, Zhan.
Afiliación
  • Shi L; Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
  • McMillan JR; Core R&D, The Dow Chemical Company, Midland, Michigan 48674, United States.
  • Yu D; Core R&D, The Dow Chemical Company, Midland, Michigan 48674, United States.
  • Chen X; Core R&D, The Dow Chemical Company, Midland, Michigan 48674, United States.
  • Tucker CJ; Core R&D, The Dow Chemical Company, Midland, Michigan 48674, United States.
  • Wasserman E; Dow Home & Personal Care, The Dow Chemical Company, Collegeville, Pennsylvania 19426, United States.
  • Mohler C; Core R&D, The Dow Chemical Company, Midland, Michigan 48674, United States.
  • Chen Z; Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.
Langmuir ; 37(36): 10806-10817, 2021 Sep 14.
Article en En | MEDLINE | ID: mdl-34455791
ABSTRACT
The performance of nonionic surfactants is mediated by the interfacial interactions at the solid-liquid interface. Here we applied sum frequency generation (SFG) vibrational spectroscopy to probe the molecular structure of the silica-nonionic surfactant solution interface in situ, supplemented by quartz crystal microbalance with dissipation monitoring (QCM-D) and molecular dynamics (MD) simulations. The combined studies elucidated the effects of nonionic surfactant solution concentration, surfactant composition, and rinsing on the silica-surfactant solution interfacial structure. The nonionic surfactants studied include ethylene-oxide (EO) and butylene oxide (BO) components with different ratios. It was found that the CH groups of the surfactants at the silica-surfactant solution interfaces are disordered, but the interfacial water molecules are ordered, generating strong SFG OH signals. Solutions with higher concentrations of surfactant lead to a slightly higher amount of adsorbed surfactant at the silica interface, resulting in more water molecules being ordered at the interface, or a higher ordering of water molecules at the interface, or both. MD simulation results indicated that the nonionic surface molecules preferentially adsorb onto silanol sites on silica. A surfactant with a higher EO/BO ratio leads to more water molecules being ordered and a higher degree of ordering of water molecules at the silica-surfactant solution interface, exhibiting stronger SFG OH signal, although less material is adsorbed according to the QCM-D data. A thin layer of surfactants remained on the silica surface after multiple water rinses. To the best of our knowledge, this is the first time the combined approaches of SFG, QCM-D and MD simulation techniques have been applied to study nonionic surfactants at the silica-solution interface, which enhances our understanding on the interfacial interactions between nonionic surfactants, water and silica. The knowledge obtained from this study can be helpful to design the optimal surfactant concentration and composition for future applications.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Langmuir Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos