TY - JOUR
T1 - Investigations on zwitterionic alkylsulfobetaines and nonionic triton X-100 in mixed aqueous solutions
T2 - Effect on size, phase separation and mixed micellar characteristics
AU - Thakkar, Khushbu
AU - Bharatiya, Bhavesh
AU - Shah, Dinesh O.
AU - Bahadur, Pratap
PY - 2015/6/20
Y1 - 2015/6/20
N2 - Zwitterionic sulfobetaine surfactants are widely applied in industries dealing with personal care products, mainly due to an advantage of minimal irritating effects to skin as compared to ionic surfactants. We investigate on the aqueous solution behaviour of zwitterionic surfactant, namely alkyl N,N-dimethyl-3-ammonio-1-propanesulfonate (CnPS, n = 10, 12, 14, 16) in pure and mixed state with Triton X-100 (non-ionic surfactant) by using surface tensiometry, dynamic light scattering (DLS) and cloud point measurements. The critical micelle concentration (CMC) for aqueous CnPS solutions decreases with corresponding increase in alkyl chain length and is also accompanied by an increase in aggregation number. The calculated interfacial parameters for binary mixed aqueous systems involving zwitterionic surfactant and TX-100 depict almost independent behaviour of πCMC and Γmax, indicating a non-associative ideal mixing. The calculated interaction parameter (βm) for TX-100 + CnPS mixed system reveals insignificant deviation from ideal behaviour as confirmed by calculated values in proximity to zero. As concluded from size measurements using DLS, the apparent hydrodynamic size of the mixed micelles decreases with gradual addition of alkylsulfobetaines due to demicellization of formerly present ellipsoidal aggregates of TX-100. The clouding temperature of formed mixed micelles increases on gradual addition of CnPS due to corresponding increase of ionic charge and accordingly improved solubility. It is assumed that electrically neutral nature of sulfobetaines confines its electrostatic interactions with non-ionic TX-100 and accordingly deters feasible interactions leading to synergism.
AB - Zwitterionic sulfobetaine surfactants are widely applied in industries dealing with personal care products, mainly due to an advantage of minimal irritating effects to skin as compared to ionic surfactants. We investigate on the aqueous solution behaviour of zwitterionic surfactant, namely alkyl N,N-dimethyl-3-ammonio-1-propanesulfonate (CnPS, n = 10, 12, 14, 16) in pure and mixed state with Triton X-100 (non-ionic surfactant) by using surface tensiometry, dynamic light scattering (DLS) and cloud point measurements. The critical micelle concentration (CMC) for aqueous CnPS solutions decreases with corresponding increase in alkyl chain length and is also accompanied by an increase in aggregation number. The calculated interfacial parameters for binary mixed aqueous systems involving zwitterionic surfactant and TX-100 depict almost independent behaviour of πCMC and Γmax, indicating a non-associative ideal mixing. The calculated interaction parameter (βm) for TX-100 + CnPS mixed system reveals insignificant deviation from ideal behaviour as confirmed by calculated values in proximity to zero. As concluded from size measurements using DLS, the apparent hydrodynamic size of the mixed micelles decreases with gradual addition of alkylsulfobetaines due to demicellization of formerly present ellipsoidal aggregates of TX-100. The clouding temperature of formed mixed micelles increases on gradual addition of CnPS due to corresponding increase of ionic charge and accordingly improved solubility. It is assumed that electrically neutral nature of sulfobetaines confines its electrostatic interactions with non-ionic TX-100 and accordingly deters feasible interactions leading to synergism.
KW - Hydrodynamic size
KW - Ideal mixing
KW - Interfacial parameter
KW - Sulfobetaines
UR - http://www.scopus.com/inward/record.url?scp=84934970281&partnerID=8YFLogxK
U2 - 10.1016/j.molliq.2015.06.020
DO - 10.1016/j.molliq.2015.06.020
M3 - Article (Academic Journal)
AN - SCOPUS:84934970281
SN - 0167-7322
VL - 209
SP - 569
EP - 577
JO - Journal of Molecular Liquids
JF - Journal of Molecular Liquids
ER -