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Wetting and adsorption: I. The structure of adsorbed layer of nonionic surfactants at SiO 2 /water and SiO 2 /cyclohexane interface
Author(s) -
Li WaiLang,
Gao YueYing,
Xiao Li,
Gu Tiren Gu TiRen
Publication year - 1985
Publication title -
acta chimica sinica english edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 41
eISSN - 1614-7065
pISSN - 0256-7660
DOI - 10.1002/cjoc.19850030404
Subject(s) - cyclohexane , adsorption , chemistry , triton x 100 , pulmonary surfactant , monolayer , wetting , layer (electronics) , chemical engineering , hydrocarbon , molecule , chromatography , organic chemistry , biochemistry , engineering
Based on the adsorption of Triton X‐100 on silica/water and silica/cyclohexane interfaces and the adsorption of Triton X‐305 on silica/water interface, two adsorption models have been proposed. On silica/cyclohexane interface, the adsorption of Triton X‐100 is monomolecular layer. The molecules in the monolayer are presumed to be attached to the silica surface by their EO chain such that their hydrocarbon chain are exposed to the cyclohexane phase. On silica/water interface, the adsorption of Triton X‐100 or Triton X‐305 is bimolecular layer. The surfactant molecules orientated in the first layer are similar with that on the silica/cyclohexane interface. The molecules in the second layer are postulated to adsorb on those of the first in the opposite orientation, with EO chain directed toward the adsorption medium. The contact angle of quartz‐water‐cyclohexane (θ W ) as a function of the concentration of Triton X‐100 and Triton X‐305 in water has been measured with quartz plate employing the captive drop (cyclohexane) technique. The observed θ W (measured through water) rose from < 10° to a maximum of about 120° for Triton X‐100 and of about 40° for Triton X‐305 as the concentration of surfactant in water increased, and then fell, as the concentration increased further. The results are consistent with the proposed adsorption models.