Newly designed polysiloxane-graft-poly (oxyethylene) copolymeric surfactants: preparation, surface activity and emulsification properties.

Citation:

Y SELA, MAGDASSI, S, and Garti, N. 1994. “Newly Designed Polysiloxane-Graft-Poly (Oxyethylene) Copolymeric Surfactants: Preparation, Surface Activity And Emulsification Properties.”. Colloid And Polymer Science, 272, 6, Pp. 684–691. doi:10.1007/BF00659282.

Abstract:

Two sets of comb-grafted polymeric surfactants based on poly(methylhydrogen siloxane) (PHMS) and/or poly(dimethylsiloxane) (PHMS-PDMS) were prepd. by silylation of the active Si-H group with an active $ømega$-vinyl group of specially designed undecenoic-polyethylene glycol esters (UPEG) to formation "newly-designed" polysiloxane-grafted-polyethylene glycol comb-copolymeric surfactants. The hydrophilic moieties are hooked to the hydrophobic backbone through a "spacer" (undecenoic acid). The variation in the surfactants' structures were in the length and d. of the grafted hydrophilic moieties, the chain length (DP) and nature of the hydrophobic backbone. The first 12 different polymeric surfactants (set 1), termed PHMS-UPEG, were ineffective emulsifiers with limited ability to stabilize oil-in-water emulsions. The second set of surfactants, named PHMS-PDMS-UPEG comb-grafted copolymers, significantly reduced the oil-water interfacial tension and efficiently stabilized several types of oil-in-water emulsions. The best emulsifier of this set (PHMS-PDMS-52-UPEG-45), seems to be one whose anchor backbone (PHMS-PDMS) dissolves (rather than spreads) in the oil phase, and whose stabilizing moieties are sufficiently long (45 EO units) and "hooked" to the silicone backbone at high d. (52% substitution). [on SciFinder(R)]

Last updated on 05/27/2020