Surface and interfacial activities of A(B)2 star‐shaped block copolymers, where B is a polyoxirane block and A a polydiene or polyvinyl block, have been measured at 20°C. The surface tension of organic solvents is only slightly lowered by these copolymers, whereas a significant surface activity is noted in water. Interfacial tensions are dependent on both the nature of the organic solvent (aliphatic or aromatic hydrocarbons) and the molecular parameters of the copolymers; 50% polyoxirane seems to be the composition of maximum surface activity. The role played by the molecular architecture [A‐B or A(B)2] of the copolymers is demonstrated. The same limiting interfacial tension is obtained on increasing the concentration of diblock [A‐B] or star‐shaped block [A(B)2] copolymer. The limiting value is, however, attained at significantly lower concentration with the star‐shaped copolymers. Their ability to fill the interface is accordingly higher.
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Huynh‐Ba‐Gia et al. (1980) studied this question.
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