TY - JOUR
T1 - Clouding Behavior of C 13 EO x (x = 10–19) Micelles in a Wide Range of Salinity and Hardness
T2 - Concomitant Effects of Salinity and Degree of Ethoxylation
AU - Souayeh, Maissa
AU - Aoudia, Mohamed
AU - Al-Maamari, Rashid S.
N1 - Publisher Copyright:
© 2018 AOCS
PY - 2019/3
Y1 - 2019/3
N2 - The effect of salinity and degree of ethoxylation on the cloud point, T cp , in C 13 EO x (x = 10–19) micelles was investigated in distilled water and in the salinity range S = 1.96–196 g L −1 . At a fixed x value, the rate dT cp /dS was given by dT cp /dS = α b + β b S with α b < 0 and β b > 0. This trend suggests that dT cp /dS is the result of two opposing effects, an entirely (negative) surfactant-dependent effect (α b ) and a combined (positive) surfactant-solvent (β b S)-dependent effect. In addition, the rate dT cp /dS was found to become increasingly less negative with increasing salinity (dT cp /dS) < 0), suggesting an overwhelming contribution of the α b effect as compared to the β b S effect. On the other hand, at fixed S, the rate was given by dT cp /dx = α x + β x x with α x > 0 and β x < 0. This trend also suggests the existence of two opposing effects, a strictly (positive) solvent-dependent effect (α x ) and a concomitant solvent (β x )-surfactant (x)-dependent effect. Contrary to dT cp/ dS, the rate dT cp /dx was found to become increasingly less positive with increasing x values (dT cp /dx > 0), suggesting that α x is the dominant factor in the surfactants’ susceptibility to be salted in. Both constants α b and α x were attributed to a dual temperature-salinity effect on the structure of water molecules not involved in surfactant's hydration. On the other hand, β b and β x were associated with the change in the structure of water due to the dehydration of surfactants’ oxyethylene moieties with increasing temperature.
AB - The effect of salinity and degree of ethoxylation on the cloud point, T cp , in C 13 EO x (x = 10–19) micelles was investigated in distilled water and in the salinity range S = 1.96–196 g L −1 . At a fixed x value, the rate dT cp /dS was given by dT cp /dS = α b + β b S with α b < 0 and β b > 0. This trend suggests that dT cp /dS is the result of two opposing effects, an entirely (negative) surfactant-dependent effect (α b ) and a combined (positive) surfactant-solvent (β b S)-dependent effect. In addition, the rate dT cp /dS was found to become increasingly less negative with increasing salinity (dT cp /dS) < 0), suggesting an overwhelming contribution of the α b effect as compared to the β b S effect. On the other hand, at fixed S, the rate was given by dT cp /dx = α x + β x x with α x > 0 and β x < 0. This trend also suggests the existence of two opposing effects, a strictly (positive) solvent-dependent effect (α x ) and a concomitant solvent (β x )-surfactant (x)-dependent effect. Contrary to dT cp/ dS, the rate dT cp /dx was found to become increasingly less positive with increasing x values (dT cp /dx > 0), suggesting that α x is the dominant factor in the surfactants’ susceptibility to be salted in. Both constants α b and α x were attributed to a dual temperature-salinity effect on the structure of water molecules not involved in surfactant's hydration. On the other hand, β b and β x were associated with the change in the structure of water due to the dehydration of surfactants’ oxyethylene moieties with increasing temperature.
KW - Cloud point
KW - Hydrogen bonding
KW - Nonionic surfactants
KW - Salting-in effect
KW - Salting-out effect
KW - Solvent effect
KW - Surfactant effect
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U2 - 10.1002/jsde.12215
DO - 10.1002/jsde.12215
M3 - Article
AN - SCOPUS:85055045820
SN - 1097-3958
VL - 22
SP - 275
EP - 283
JO - Journal of Surfactants and Detergents
JF - Journal of Surfactants and Detergents
IS - 2
ER -