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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 272 (1994), S. 1166-1173 
    ISSN: 1435-1536
    Keywords: Gel-emulsions ; ESR spin-probe method ; order parameter ; isotropic hyperfine splitting constant ; correlation time ; stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract W/O gel-emulsions (high-internal-phase-volume-ratio emulsions) form in water (or brine) /tetraethyleneglycol dodecyl ether/heptane system above the HLB (hydrophile-lipophile balance) temperature of the system. A salt, which largely decreases cloud temperature in a water-nonionic surfactant system, makes the surfactant film rigid and the gel-emulsions hence become very stable. The effect of aded salt on the apparent order parameter “S”, and the isotropic hyperfine splitting constant “a N” in gel-emulsions was determined by the ESR spin probe method using 5-doxyl stearic acid as the spin probe. The apparent order parameter “S”, and the isotropic hyperfine splitting constant “a N” increase with increasing salinity in Na2SO4, CaCl2, and NaCl systems. It is considered that the surfactant molecules are tightly packed in these systems and this tendency is highly related to the stability of gel-emulsions. The salt dehydrates the hydrophilic moiety of surfactant and hence the lateral interactions of surfactant molecular layer at the water-oil interface increases. The observed difference in the apparent order parameter between the ordinary emulsions and the gel-emulsions suggests that most of the surfactant molecules are adsorbed at the oil-water interface (the surface of the water droplet) in gel-emulsions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 277 (1999), S. 1117-1124 
    ISSN: 1435-1536
    Keywords: Key words Adsorption manner ; Phase separation ; Resolubilization ; Electrostatic interaction and intraction ; Scaling law
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Aqueous mixtures of anionic surfactants with cationically substituted quaternary ammonium derivatives of hydroxyethylcellulose, JR and LR series, were investigated by several techniques. On adding sodium dodecyl sulfate (SDS) to a polyelectrolyte solution, phase separation with precipitation occurs in a co-operative way, and redissolution of precipitation is observed at the critical micelle concentration (CMC) of SDS. This is due to admicelle formation on the polyelectrolyte. The phase separation for the two-headed anionic surfactant systems is also seen, while the concentration where this takes place is near the CMC of the surfactant. This is remarkable in the case of the triethanolamine cocoyl glutamate (TCG)–JR 400 system, in which TCG has a CMC over 1 order of magnitude smaller CMC than that of SDS. Surface tension and the dynamic light scattering measurements show the existence of not only electrostatic interaction between the cationic polyelectrolyte and the two-headed anionic surfactant but also intraction between the adsorbed polymers. The scaling analysis of the precipitation line of the surfactant with polyelectrolyte concentration elucidates that one molecule of TCG can neutralize approximately two charges on JR 400.
    Type of Medium: Electronic Resource
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