Energy efficient polyolefin process
US-9221920-B2 · Dec 29, 2015 · US
US9085648B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9085648-B2 |
| Application number | US-201314136934-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2013 |
| Priority date | Oct 8, 2008 |
| Publication date | Jul 21, 2015 |
| Grant date | Jul 21, 2015 |
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The present invention relates to a continuous process for the production of a superabsorbent polymer comprising providing an acidic liquid aqueous monomer mixture containing dissolved oxygen; continuously feeding the aqueous monomer mixture to a reactor; introducing a source of carbonate or hydrogen carbonate into the aqueous monomer mixture prior to entry into the reactor thereby forming a gas phase comprising carbon dioxide and at least a part of the dissolved oxygen, the gas phase being dispersed in the liquid phase; subjecting the gas/liquid mixture to at least partial phase separation immediately prior to or after entry into the reactor and at least partially removing the separated gaseous phase; subjecting the liquid phase in the reactor to free-radical polymerization to obtain the superabsorbent polymer, and continuously removing the superabsorbent polymer from the reactor.
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The invention claimed is: 1. A continuous process for the production of a superabsorbent polymer comprising: (a) providing an acidic liquid aqueous monomer mixture containing dissolved oxygen, whereby the monomers are selected to provide after polymerization a superabsorbent polymer whereby the aqueous monomer mixture comprises at least one ethylenically unsaturated acid and at least one monomer bearing at least two ethylenically unsaturated groups and whereby the at least one ethylenically unsaturated acid is at least partially neutralized, (b) continuously feeding said aqueous monomer mixture to a reactor, (c) introducing a source of carbonate or hydrogen carbonate into said aqueous monomer mixture prior to entry into the reactor thereby forming a gas phase comprising carbon dioxide and at least a part of said dissolved oxygen, said gas phase being dispersed in said aqueous monomer mixture whereby the source of carbonate or hydrogen carbonate is introduced in an amount to result in from about 1 to about 15% of the total neutralization of the acidic functionality of the resultant superabsorbent polymer to achieve the respective degree of neutralization of the resultant superabsorbent polymer, (d) subjecting said gas and aqueous monomer mixture to at least partial phase separation creating a second gas phase comprising the resulting product of oxygen and carbonate or hydrogen carbonate and a liquid phase immediately prior to or after entry into the reactor and at least partially removing the separated second gas phase, (e) subjecting the liquid phase in the reactor to free-radical polymerization to obtain the superabsorbent polymer, and (f) continuously removing the superabsorbent polymer from the reactor. 2. The process of claim 1 , whereby the aqueous monomer mixture is fed to the reactor via a transfer line and wherein the pressure difference between said transfer line and reactor is from about 0.5 to about 5 bar. 3. The process according to claim 1 , whereby the free-radical polymerization is initiated by a redox initiator and wherein the oxidative component of the redox initiator is added to the monomer mixture in step (a) and the reductive component of the redox initiator is added to the monomer mixture after step (c) prior to the monomer mixture entry into the reactor or the reductive component of the redox initiator is added directly to the reactor at a position in proximity to the entry point of the monomer mixture. 4. The process according to claim 1 , whereby the reactor encompasses at least three zones, wherein the first zone is an initiation zone, the second zone is a gel-phase zone and the third zone is a granulation zone and the monomer mixture is fed to the initiation zone. 5. The process according to claim 1 , whereby the reactor is selected from continuous kneaders and extruders or belt reactors. 6. The process according to claim 1 , whereby no additional inert gas is introduced in either of steps (a), (b), and (c) or no additional inert gas is introduced into the reactor or no additional inert gas is introduced at any point of the process. 7. The process according to claim 1 , whereby fines of a superabsorbent polymer having a particle size of less than about 300 μm are added to the aqueous monomer mixture prior to the introduction of the source of carbonate or hydrogen carbonate. 8. The process according to claim 1 , whereby at least one carbon dioxide containing off-gas stream withdrawn from the reactor is subjected to scrubbing with a basic aqueous solution in a scrubber prior to venting thereby forming a carbonate or hydrogen carbonate containing aqueous scrubber solution. 9. The process according to claim 1 , whereby said source of carbonate or hydrogen carbonate comprises an aqueous solution of any one of an alkali metal carbonate, hydrogen carbonate, or mixtures thereof. 10. The process according to claim 8 , wherein said source of carbonate or hydrogen carbonate further comprises said aqueous scrubber solution of any one of an alkali metal carbonate, hydrogen carbonate, or mixtures thereof. 11. The process of claim 8 , whereby the source of carbonate or hydrogen carbonate is at least a part of said carbonate or hydrogen carbonate containing aqueous scrubber solution. 12. The process according to claim 1 , further comprising: (g) withdrawing at least one carbon dioxide containing off-gas stream from the reactor, (h) subjecting said carbon dioxide containing off-gas stream to scrubbing with a basic aqueous solution in a scrubber prior to venting thereby forming a carbonate or hydrogen carbonate containing aqueous scrubber solution, (i) drying the superabsorbent polymer, (j) grinding and classifying the dried superabsorbent polymer thereby removing fines having a particle size of less than about 300 μm, (k) recycling said fines to the monomer mixture prior to the introduction of the source of carbonate or hydrogen carbonate, whereby at least a part of the carbonate or hydrogen carbonate containing aqueous scrubber solution obtained in (h) is introduced as source of carbonate or hydrogen carbonate in (c). 13. The process according to claim 1 , wherein the resultant superabsorbent polymer is surface modified by surface post-crosslinking, heat-treatment, by additives, or any combination thereof. 14. A superabsorbent polymer comprising the superabsorbent polymer made by the process of claim 1 . 15. A superabsorbent polymer comprising the superabsorbent polymer made by the process of claim 12 .
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