Synthesis, Characterization and Properties of Novel Amphiphilic Phosphated Ionomers by Ring‐Opening Reaction of Epoxidized Styrene‐Butadiene‐Styrene Triblock Polymer

A method for synthesis of novel phosphated ionomer of (styrene‐butadiene‐styrene) triblock polymer (SBS) from epoxidized SBS was developed. The optimum conditions for the ring‐opening reaction of the epoxidized SBS with aqueous solution of disodium hydrogen phosphate were studied. It was found that during the ring‐opening reaction phase transfer catalyst, ring‐opening catalyst and pH regulator were necessary to enhance the conversion of epoxy groups to ionic groups. The products were characterized with Fourier Transform Infrared Spectrophotometry (FTIR) and transmission electron microscopy (TEM). Some properties of the phosphated ionomer were studied. With increasing ionic groups or the ionic potential of the cation of the ionomer, the water absorbency emulsifying volume and the intrinsic viscosity of the ionomer increase, whereas the oil absorbency decreases. The ionomer possesses excellent emulsifying property, as compared with the sulfonated ionomer. The disodium phosphated ionomers in the presence of 10% zinc stearate showed better mechanical properties than the original epoxy SBS. Optimum mechanical properties occurred at the ionic group content of 0.95 mmol/g ionomer. When the ionomer was blended with crystalline polypropylene, a synergistic effect occurs with respect to the tensile strength. The ionomer behaves as a compatibilizer for blending equal amount of SBS and oil‐resistant chlorohydrin rubber (CHR) to form an oil resistant thermoplastic elastomer. SEM microphotographs indicated enhanced compatibility between the two components of the blend in the presence of the ionomer.

[1]  Wei Yang,et al.  A Novel Method for Synthesis of Sulfonated SBS Ionomers by Ring-Opening Reaction of Epoxidized SBS, Their Characterization, Properties, and Blends , 2007 .

[2]  D. Xie,et al.  Synthesis of Maleated Ionomers via Ring‐Opening Reaction of Epoxidized (Styrene‐Butadiene‐Styrene) Triblock Copolymer with Potassium Hydrogen Maleate and Study of their Properties , 2007 .

[3]  Wei Yang,et al.  Synthesis of sulfonated rubber ionomers by the ring‐opening reaction of epoxidized styrene–butadiene rubber, their characterization, and their properties , 2006 .

[4]  D. Xie,et al.  Preparation, characterization, and some properties of ionomers from a sulfonated styrene–butadiene–styrene triblock copolymer without gelation , 2005 .

[5]  I. Capek Dispersions of polymer ionomers: I. , 2004, Advances in colloid and interface science.

[6]  J. Samuel,et al.  High Styrene–Rubber Ionomers, an Alternative to Thermoplastic Elastomers , 2002 .

[7]  J. Brosse,et al.  Alcoholysis of epoxidized polyisoprenes by direct opening of oxirane rings with alcohol derivatives. 1. Modelization of the reaction , 2001 .

[8]  S. De,et al.  IONIC THERMOPLASTIC ELASTOMERS: A REVIEW , 2001 .

[9]  A. K. Banthia,et al.  A novel synthesis of sulfonated polybutadiene ionomer by a phase‐transfer catalyst , 1999 .

[10]  Junshi Guo,et al.  Melt flow and mechanical properties of sulfonated SBR ionomers and their polymer blends , 1995 .

[11]  Jean-Claude Soutif,et al.  Modification au deuxième degrá de polymères époxydés, 4. Fixation de i'acide naphtylacétique sur polyisoprène‐1,4 de synthèse et caoutchouc naturel liquide époxydés , 1992 .

[12]  H. Xie,et al.  Polymer blends with two kinds of elastomeric ionomers , 1991 .

[13]  H. Xie,et al.  Melt flow and mechanical properties of sulfonated butyl rubber ionomers , 1990 .

[14]  B. Ma,et al.  Properties of sulfonated EPDM lonomers obtained by sulfonation in the presence of phase-transfer catalyst , 1989 .

[15]  R. Weiss,et al.  Synthesis, Properties, and Structure of Sulfonate Ionomers , 1988 .

[16]  S. Siggia Quantitative Organic Analysis Via Functional Groups , 1963 .

[17]  K. G. Stone Quantitative organic analysis via functional groups , 1954 .