Adsorption of Cationic and Anionic Surfactants on Cyclopentane Hydrates

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This work presents the adsorption of an anionic surfactant, sodium dodecyl sulfate (SDS), and a cationic one, dodecyl-trimethylammonium bromide (DTAB), on cyclopentane (CP) hydrates Adsorption isotherms were obtained by liquid liquid titrations. Also, the adsorption was qualitatively studied by zeta potential measurements. The isotherm of both SDS and DTAB exhibits a two-plateau (L-S) type The saturated adsorption amount in the first step (Langmuir type) is 0 01 and 0.03 mmol g(-1) for SDS and DTAB, respectively. The Langmuir equilibrium constant is 1.17 mM(-1) for SDS and 0.32 mM(-1) for DTAB. The maximum adsorption amount of SDS in the second step (S type) is 2 5 times higher than that in the Langmuir step The similar trend is observed for DTAB. SIDS adsorption shifts the zeta potential from -60 to -90 mV in the first step, followed by a further 30 mV decrease as the adsorption approaches the second plateau For DTAB, the zeta potential increases from -60 to 50 mV in the Langmuir step and then it approaches 90 mV in the second step On the basis of these results, the role of surfactants in enclathration is discussed and the adsorption mechanism of surfactant on clathrate hydrates is also presented.
Publisher
AMER CHEMICAL SOC
Issue Date
2010-08
Language
English
Article Type
Article
Keywords

SODIUM DODECYL-SULFATE; METHANE; INTERFACE; KINETICS; POINT

Citation

JOURNAL OF PHYSICAL CHEMISTRY C, v.114, no.31, pp.13385 - 13389

ISSN
1932-7447
DOI
10.1021/jp102846d
URI
http://hdl.handle.net/10203/174967
Appears in Collection
CBE-Journal Papers(저널논문)
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