Sulfonation ethylene-propylene-diene terpolymers

S-EPDM Sulfonated ethylene-propylene-diene terpolymers... 

S-EPDM Sulfonated ethylene- propylene-diene terpolymer... 

Copoly(ethylene/methacrylic acid) Copoly(butadiene/acrylic acid) Perfluorsulfonate ionomer Perfluorocarboxylate ionomer Telechelic polybutadiene ionomer Chlorosulfonated polyethylene Sulfonated ethylene/propylene/diene terpolymer... 

The term ionomer is used to describe a variety of copolymers consisting primarily of hydrocarbon backbones to which are attached a relatively small number of ionizable branches. This family of polymers includes two groups that are ethylene-based, one based on ethylene-co-methaciylic acid copolymer and the other on sulfonated ethylene-propylene-diene terpolymer. The latter is an essentially noncrystalline mbber that is beyond the scope of the semicrystalline materials covered in this work (the synthesis, properties, and structure of sulfonate ionomers are reviewed in Ref 90). lonomers based on partially or completely... 

Sulfonation is very useful chemical modification of polymer, as it induces high polarity in the polymer changing its chemical as well as physical properties. Sulfonated polymers are also important precursors for ionomer formation [75]. There are reports of sulfonation of ethylene-propylene diene terpolymer (EPDM) [76, 77], polyarylene-ether-sulfone [78], polyaromatic ether ketone [79], polyether ether ketone (PEEK) [80], styrene-ethylene-butylene-styrene block copolymer, (SEBS) [81]. Poly [bis(3-methyl phenoxy) phosphozene] [82], Sulfonated polymers show a distinct peak at 1176 cm"1 due to stretching vibration of 0=S=0 in the -S03H group. Another peak appears at 881 cm 1 due to stretching vibration of S-OH bond. However, the position of different vibrational bands due to sulfonation depends on the nature of the cations as well as types of solvents [75, 76]. 

Arguably the most important amorphous ionomer is sulfonated polystyrene (SPS). Other ionomers include poly(styrene-rfln-methacrylic acid) (SMAA), polyurethanes, siloxanes, butadiene-based elastomers, ethylene-propylene-diene terpolymers, acrylates and methacrylates, polyphosphoesters, polyimides, and many others. ... 

This technique has found the following applications in addition to those discussed in Sections 10.1 (resin cure studies on phenol urethane compositions) [65], 12.2 (photopolymer studies [66-68]), and 13.3 (phase transitions in PE) [66], Chapter 15 (viscoelastic and rheological properties), and Section 16.4 (heat deflection temperatures) epoxy resin-amine system [67], cured acrylate-terminated unsaturated copolymers [68], PE and PP foam [69], ethylene-propylene-diene terpolymers [70], natural rubbers [71, 72], polyester-based clear coat resins [73], polyvinyl esters and unsaturated polyester resins [74], polyimide-clay nanocomposites [75], polyether sulfone-styrene-acrylonitrile, PS-polymethyl methacrylate (PMMA) blends and PS-polytetrafluoroethylene PMMA copolymers [76], cyanate ester resin-carbon fibre composites [77], polycyanate epoxy resins [78], and styrenic copolymers [79]. 

Carbon nanotubes are being increasingly used for the reinforcement of plastics, including epoxy resins [57-59], polyamides [55, 60-62], polyimides [63], poly-silsesquioxane [64], polycaprolactam [65], polyethylene oxide [66], polyethylene [67, 55,62], polyurethane [67], ethylene-vinyl acetate [69-73], polyhydroxybutylene-co-hydroxyvalerate [75], ethylene-propylene diene terpolymer [73], and sulfonated polyarylene sulfone [53]. 

Tg measurements have been performed on many other polymers and copolymers including phenol bark resins [71], PS [72-74], p-nitrobenzene substituted polymethacrylates [75], PC [76], polyimines [77], polyurethanes (PU) [78], Novolac resins [71], polyisoprene, polybutadiene, polychloroprene, nitrile rubber, ethylene-propylene-diene terpolymer and butyl rubber [79], bisphenol-A epoxy diacrylate-trimethylolpropane triacrylate [80], mono and dipolyphosphazenes [81], polyethylene glycol-polylactic acid entrapment polymers [82], polyether nitrile copolymers [83], polyacrylate-polyoxyethylene grafts [84], Novolak type thermosets [71], polyester carbonates [85], polyethylene naphthalene, 2,6, dicarboxylate [86], PET-polyethylene 2,6-naphthalone carboxylate blends [87], a-phenyl substituted aromatic-aliphatic polyamides [88], sodium acrylate-methyl methacrylate multiblock copolymers [89], telechelic sulfonate polyester ionomers [90], aromatic polyamides [91], polyimides [91], 4,4"-bis(4-oxyphenoxy)benzophenone diglycidyl ether - 3,4 epoxycyclohexyl methyl 3,4 epoxy cyclohexane carboxylate blends [92], PET [93], polyhydroxybutyrate [94], polyetherimides [95], macrocyclic aromatic disulfide oligomers [96], acrylics [97], PU urea elastomers [97], glass reinforced epoxy resin composites [98], PVOH [99], polymethyl methacrylate-N-phenyl maleimide, styrene copolymers [100], chiral... 

The curing process was analyzed by means of a rheometry test. The rheograms of ethylene-propylene-diene composites show that the maximum for a sample of sul-fonated ethylene-propylene-norbomene was three times higher than that for virgin ethylene-propylene-norbomene terpolymer. This result suggests that the incorporation of sulfonate groups onto the carbon nanotube surface reduces the cross-limiting efficiency of the benzoyl peroxide catalyst used in the preparation. 

Copolymers of an acrylate and a small amount of other monomer which provides vulcanizability Copolymers fan acrylate and acrylonitrile Chloro-polyethylene Polychloro-trifluoro-ethylene Chloro-sulfonly-polyethylene Terpolymers of ethylene, propylene and a nonconjugated diene which results in pendant unsaturation (not in the main chain)... 

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