POLYMERIC DECONTAMINANT: N,N-DICHLORO POLY (STYRENE-CO-DIVINYL BENZENE) SULFONAMIDE-SYNTHESIS, CHARACTERIZATION AND EFFICACY AGAINST SIMULANT OF SULFUR MUSTARD

N,N-Dichloro poly(styrene-co-divinylbenzene) sulfonamide (1) reacts with 2-chloro ethyl phenyl sulfide (2), a simulant of sulfur mustard (SM), at room temperature, yielding corresponding nontoxic sulfones and sulfoxides in aqueous as well as aprotic medium. The decontamination reaction was monitored by gas chromatography, and products were identified by gas chromatography–mass spectrometry. N,N-dichloro poly(styrene-co-divinylbenzene) sulfonamide was synthesized by three steps from a commercial starting material sulfonate cation-exchange resin and characterized by FTIR, and TGA, and compressive strength by universal testing machine. The positive chlorine content of this polymer was checked by standard iodometry titration. The synthesized positive chlorine compound is observed to be a promising against a simulant of SM, chiefly in the situation where use of aqueous medium is precluded. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007

[1]  K. Pepper Sulphonated cross‐linked polystyrene: A monofunctional cation‐exchange resin , 2007 .

[2]  A. Shaplov,et al.  Ionic-liquid-promoted Michaelis-Arbuzov rearrangement , 2006 .

[3]  D. Sherrington,et al.  High surface area polystyrene resin-supported Pt catalysts in room temperature solventless octene hydrosilylation using methyldichlorosilane , 2002 .

[4]  E. Kociołek-Balawejder A macromolecular N,N-dichlorosulfonamide as oxidant for residual sulfides , 2002 .

[5]  David R. Brown,et al.  Acidities and catalytic activities of persulfonated poly(styrene-co-divinylbenzene) ion-exchange resins , 2001 .

[6]  Anilesh Kumar,et al.  Effect of chemical modifications upon exchange capacity of aminated macroporous styrene–divinyl benzene (PS–DVB) copolymer anion exchange resin , 2001 .

[7]  E. Kociołek-Balawejder A macromolecular N,N-dichlorosulfonamide as oxidant for thiocyanates , 2000 .

[8]  E. Kociołek-Balawejder A macromolecular N,N-dichlorosulfonamide as oxidant for cyanides , 2000 .

[9]  Jou‐Hyeon Ahn,et al.  HOLLOW GELULAR BEADS OF STYRENE-DIVINYLBENZENE COPOLYMER PREPARED BY SUSPENSION POLYMERIZATION , 1996 .

[10]  D. K. Dubey,et al.  Degradation of 2,2'-dihalodiethyl sulfides(mustards) by N,N-dichloro-4-methylbenzenesulphonamide in aprotic medium , 1993 .

[11]  James A. Baker,et al.  Decontamination of chemical warfare agents , 1992 .

[12]  R. Arshady Beaded polymer supports and gels: I. Manufacturing techniques , 1991 .

[13]  E. Kociołek-Balawejder,et al.  Studies on a macromolecular dichloroamine — the N,N‐dichloro poly(styrene‐co‐divinylbenzene) sulphonamide , 1989 .

[14]  J. Fritz,et al.  Selectivity behavior of low-capacity, partially sulfonated, macroporous resin beads , 1974 .

[15]  S. Ōae,et al.  Sulfilimine. I. Synthesis and Formation Mechanism , 1969 .

[16]  M. Salunkhe,et al.  Polymer-supported analogues of halogeno-sulphonamides preparation and applications in synthetic organic chemistry , 1991 .

[17]  J. R. Millar 263. Interpenetrating polymer networks. Styrene–divinylbenzene copolymers with two and three interpenetrating networks, and their sulphonates , 1960 .

[18]  M. Young,et al.  833. Properties of ion-exchange resins in relation to their structure. Part VI. Anion-exchange resins derived from styrene-divinyl-benzene copolymers , 1953 .

[19]  A. Vogel,et al.  A text-book of quantitative inorganic analysis : theory and practice , 1951 .