TY - JOUR
T1 - Clouding Behavior of C13EOx (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
PY - 2018/1/1
Y1 - 2018/1/1
N2 - The effect of salinity and degree of ethoxylation on the cloud point, Tcp, in C13EOx (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 dTcp/dS was given by dTcp/dS = αb + βbS with αb < 0 and βb > 0. This trend suggests that dTcp/dS is the result of two opposing effects, an entirely (negative) surfactant-dependent effect (αb) and a combined (positive) surfactant-solvent (βbS)-dependent effect. In addition, the rate dTcp/dS was found to become increasingly less negative with increasing salinity (dTcp/dS) < 0), suggesting an overwhelming contribution of the αb effect as compared to the βbS effect. On the other hand, at fixed S, the rate was given by dTcp/dx = αx + βxx with αx > 0 and βx < 0. This trend also suggests the existence of two opposing effects, a strictly (positive) solvent-dependent effect (αx) and a concomitant solvent (βx)-surfactant (x)-dependent effect. Contrary to dTcp/dS, the rate dTcp/dx was found to become increasingly less positive with increasing x values (dTcp/dx > 0), suggesting that αx is the dominant factor in the surfactants’ susceptibility to be salted in. Both constants αb and αx were attributed to a dual temperature-salinity effect on the structure of water molecules not involved in surfactant's hydration. On the other hand, βb and βx 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, Tcp, in C13EOx (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 dTcp/dS was given by dTcp/dS = αb + βbS with αb < 0 and βb > 0. This trend suggests that dTcp/dS is the result of two opposing effects, an entirely (negative) surfactant-dependent effect (αb) and a combined (positive) surfactant-solvent (βbS)-dependent effect. In addition, the rate dTcp/dS was found to become increasingly less negative with increasing salinity (dTcp/dS) < 0), suggesting an overwhelming contribution of the αb effect as compared to the βbS effect. On the other hand, at fixed S, the rate was given by dTcp/dx = αx + βxx with αx > 0 and βx < 0. This trend also suggests the existence of two opposing effects, a strictly (positive) solvent-dependent effect (αx) and a concomitant solvent (βx)-surfactant (x)-dependent effect. Contrary to dTcp/dS, the rate dTcp/dx was found to become increasingly less positive with increasing x values (dTcp/dx > 0), suggesting that αx is the dominant factor in the surfactants’ susceptibility to be salted in. Both constants αb and αx were attributed to a dual temperature-salinity effect on the structure of water molecules not involved in surfactant's hydration. On the other hand, βb and βx 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
JO - Journal of Surfactants and Detergents
JF - Journal of Surfactants and Detergents
ER -