Manufacturing method and use for chlorinated polyvinyl chloride resin
US-2024010762-A1 · Jan 11, 2024 · US
US11965053B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11965053-B2 |
| Application number | US-202118265885-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 10, 2021 |
| Priority date | Dec 11, 2020 |
| Publication date | Apr 23, 2024 |
| Grant date | Apr 23, 2024 |
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A process for producing a halogenated isoolefin copolymer involves contacting an unsaturated isoolefin copolymer cement, the cement comprising an unsaturated isoolefin copolymer dissolved in an organic solvent, under halogenation conditions with a halogenating agent and an aqueous solution of a potassium salt-based oxidant to form a two-phase reaction medium comprising an organic phase and an aqueous phase, the oxidant capable of converting hydrogen halide to free halogen. The process provides improved halogen recovery, is less sensitive to the presence of water, and makes use of more stable and less environmentally damaging oxidants.
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What is claimed is: 1. A process for producing a halogenated isoolefin copolymer, the process comprising contacting an unsaturated isoolefin copolymer cement, the cement comprising an unsaturated isoolefin copolymer dissolved in an organic solvent, under halogenation conditions with a halogenating agent and an aqueous solution of a potassium salt-based oxidant to form a two-phase reaction medium comprising an organic phase and an aqueous phase, the potassium salt-based oxidant capable of converting hydrogen halide to free halogen. 2. The process of claim 1 , wherein in the potassium salt-based oxidant comprises KHSO 5 , K 2 S 2 O 8 , KCIO, KBrO, KBrO 3 , KIO 3 , KCIO 3 , KCIO 4 , KIO 4 , compounds that generate the aforementioned potassium salt-based oxidants, or mixtures thereof. 3. The process of claim 1 , wherein in the potassium salt-based oxidant comprises potassium peroxymonosulfate. 4. The process of claim 1 , wherein in the potassium salt-based oxidant comprises KHSO 5 . 5. The process of claim 1 , wherein the cement has a water content of 1 wt % or greater based on total weight of the cement. 6. The process of claim 5 , wherein the water content of the cement is 1.5 wt % or greater. 7. The process of claim 5 , wherein the water content of the cement is 1-30 wt %. 8. The process of claim 5 , wherein the water content of the cement is 2-20 wt % and the potassium salt-based oxidant comprises KHSO 5 . 9. The process of claim 1 , wherein the aqueous solution further comprises a phase transfer catalyst. 10. The process of claim 9 , wherein the phase transfer catalyst comprises a molecule having at least seven oxygen atoms that are available to form a complex with a potassium ion. 11. The process of claim 9 , wherein the phase transfer catalyst comprises a polyalkylene oxide ether. 12. The process of claim 9 , wherein the phase transfer catalyst comprises a non-ionic surfactant having a first chain that is a hydrocarbon chain connected to a second chain comprising from 3 to 20 ethylene oxide units. 13. The process of claim 9 , wherein the potassium salt-based oxidant and phase transfer catalyst are present in the aqueous solution in a molar ratio in a range of 1:3 to 100:1. 14. The process of claim 1 , wherein the unsaturated isoolefin copolymer cement is produced by polymerizing at least one isoolefin monomer and at least one copolymerizable unsaturated monomer in an organic diluent and removing the organic diluent and residual monomers by flash separation with steam. 15. The process of claim 14 , wherein the at least one isoolefin monomer is isobutene and the at least one copolymerizable unsaturated monomer is isoprene, p-methyl styrene or β-pinene. 16. The process of claim 14 , wherein the at least one isoolefin monomer is isobutene and the at least one copolymerizable unsaturated monomer is isoprene, and the unsaturated isoolefin copolymer further comprises one or more additional copolymerizable monomers selected from the group consisting of α-methyl styrene, p-methyl styrene, chlorostyrene, cyclopentadiene, methylcyclopentadiene and indene. 17. The process of claim 14 , wherein the organic diluent comprises methyl chloride. 18. The process of claim 1 , wherein the halogenating agent is Br 2 . 19. The process of claim 1 , wherein the unsaturated isoolefin copolymer is present in the reaction medium in an amount of 10-33 wt %, based on total weight of the two-phase reaction medium. 20. The process of claim 1 , wherein the contacting the unsaturated isoolefin copolymer cement with the halogenating agent is conducted for 1-60 minutes at a temperature in a range of 20-60° C.
by reaction with free halogens · CPC title
Metalic sodium or potassium · CPC title
with conjugated diolefins, e.g. butyl rubber · CPC title
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