Claims
- 1. A process for sulfonating an unsaturated polymer to form a sulfonated polymer, which comprises the steps of:
- (a) forming a cement of said unsaturated polymer in a non-reactive solvent; and
- (b) contacting said cement with a sulfonating agent at a temperature of about -100.degree. C. to about +100.degree. C. for a sufficient period of time to form a sulfonated polymer having about 15 to about 50 meq. of sulfonate groups per 100 grams of said sulfonated polymer, said sulfonating agent being a mixture of RCO.sub.2 SO.sub.3 H and a second reagent which is selected from the group consisting of (RCO).sub.2 O and RCO.sub.X, a molar ratio of said second reagent to said RCO.sub.2 SO.sub.3 H being at least about one, wherein R is selected from the group consisting of CH.sub.3 --, C.sub.2 H.sub.5 --, C.sub.3 H.sub.7 --, C.sub.4 H.sub.9 --, C.sub.5 H.sub.11 --, C.sub.6 H.sub.13 --, and C.sub.6 H.sub.5 CH.sub.2 and mixtures thereof, and X is selected from the group consisting of F, Cl and Br.
- 2. The process of claim 1, wherein such sulfonating agent is formed prior to addition to said cement.
- 3. The process of claim 1, wherein said sulfonating agent is formed in situ in said cement.
- 4. The process of claim 1, wherein such sulfonating agent is formed from a mixture of said (RCO).sub.2 O and concentrated H.sub.2 SO.sub.4.
- 5. The process of claim 1, wherein said sulfonating agent is formed from a mixture of said (RCO).sub.2 O, RCOCl and H.sub.2 SO.sub.4.
- 6. The process of claim 1, wherein said sulfonating agent is formed from a mixture of said (RCO).sub.2 O and ClSO.sub.3 H.
- 7. The process of claim 1, wherein such sulfonating agent is formed from a mixture of RCOCl and H.sub.2 SO.sub.4.
- 8. The process according to claim 1, wherein said cement contains at least about 0.1 wt. % of water.
- 9. The process according to claim 1, wherein said elastomeric polymer is neoprene.
- 10. The process according to claim 1, wherein said elastomeric polymer is selected from the group consisting of Butyl rubbers, styrene-butadiene copolymers, isoprene-styrene copolymers, and EPDM terpolymers.
- 11. The process according to claim 1, wherein said sulfonated elastomeric polymer has about 20 to about 40 meq. sulfonate groups per 100 grams of said sulfonated elastomeric polymer.
- 12. The process according to claim 1, further including neutralizing at least about 95% of said sulfonate groups with a metal counterion selected from the group consisting of antimony, iron, lead and Groups I-A, II-A, I-B and II-B of the Periodic Table of Elements and mixtures thereof.
- 13. The process according to claim 12, further including adding an ionic plasticizer at a concentration level of at least about 3 parts by weight per 100 parts by weight of said neutralized sulfonated elastomeric polymer.
- 14. The process according to claim 13 further including an additive to said neutralized sulfonated elastomeric polymer at a concentration level of less than about 300 parts by weight per 100 parts by weight of said neutralized sulfonated elastomeric polymer.
- 15. The process according to claim 14, wherein said additive is selected from the group consisting of oils, fillers, waxes, pigments, a metallic hydroxide and stabilizers and mixtures thereof.
- 16. The process according to claim 1, wherein said non-reactive solvent is selected from the group consisting of aliphatic hydrocarbons, chlorinated aliphatics, aromatic hydrocarbons, and chlorinated aromatic hydrocarbons and mixtures thereof.
- 17. The process of claim 1 wherein at least 70% of the amount of sulfonating agent present in the reaction zone that does not exceed the stoichiometric amount of sulfonating agent required to react with all available sites of unsaturation in said elastomeric polymer is converted to sulfonate groups on said elastomeric polymer.
- 18. The process of claim 1, wherein said elastomeric polymer dissolved in such non-reactive solvent contains at least 0.2 wt. % water.
CROSS-REFERENCE TO RELATED APPLICATION
This application is a continuation-in-part of copending application Ser. No. 855,701 filed Nov. 29, 1977 now abandoned.
US Referenced Citations (4)
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
855701 |
Nov 1977 |
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