Resin for precipitation of minerals and salts, methods of manufacture and uses thereof

US9879120B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9879120-B2
Application numberUS-200913266380-A
CountryUS
Kind codeB2
Filing dateApr 27, 2009
Priority dateApr 27, 2009
Publication dateJan 30, 2018
Grant dateJan 30, 2018

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  1. Title

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  5. First independent claim

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Abstract

Official abstract text for this publication.

A method of producing a scale-control resin including combining in an aqueous solution a cation-exchange resin and a weak-acid anion mineral or salt having a multivalent cation to allow ion exchange between the resin and the multivalent cation. The cation-exchange resin may be a weak-acid ion exchange resin. The method may further include adding a strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt to the aqueous solution.

First claim

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The invention claimed is: 1. A method of producing a scale-control resin comprising combining in an aqueous solution a hydrogen-functionalized weak-acid cation-exchange resin, a weak-acid anion mineral or salt having a multivalent cation, and a strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt, wherein ions are exchanged between the resin and the weak-acid anion mineral or salt by a catalyzed reaction to produce the scale-control resin that is multivalent cation-functionalized. 2. The method of claim 1 , wherein during the catalyzed reaction the aqueous solution of the weak-acid cation-exchange resin, the weak-acid anion mineral or salt, and the strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt is heated. 3. The method of claim 2 wherein during the catalyzed reaction the aqueous solution of the weak-acid cation-exchange resin, the weak-acid anion mineral or salt, and the strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt is heated to a temperature between 50 and 100° C. 4. The method of claim 2 wherein the combination of the aqueous solution of the weak-acid cation-exchange resin, the weak-acid anion mineral or salt, and the strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt is heated to a temperature between 70 and 90° C. 5. The method of claim 1 further comprising drying the scale-control resin to a moisture content selected to increase the scale control efficiency of the scale-control resin. 6. The method of claim 5 , wherein the scale-control resin is dried to a moisture content of less than 50%. 7. The method of claim 5 , wherein the scale-control resin is dried to a moisture content of between 5 and 20%. 8. The method of claim 1 wherein the weak-acid anion mineral or salt comprises calcium carbonate. 9. The method of claim 1 wherein the strong-acid salt comprises calcium chloride. 10. The method of claim 1 wherein the weak-acid anion mineral or salt comprises aluminum hydroxycarbonate hydrate. 11. The method of claim 1 wherein the strong-acid salt comprises aluminum sulfate. 12. The method of claim 1 , wherein the weak-acid anion mineral or salt comprises an anion selected from the group consisting of carbonate and bicarbonate. 13. The method of claim 1 wherein the strong-acid salt comprises an anion selected from the group consisting of chloride, sulfate, nitrate, bromide, iodide and perchlorate. 14. The method of claim 1 , wherein the weak-acid anion mineral or salt is added in stoichiometric excess as compared to the cation-exchange capacity of the cation-exchange resin. 15. The method of claim 1 , wherein a less than stoichiometric quantity of the strong-acid salt as compared to the weak-acid anion mineral or salt is added to the aqueous solution. 16. The method of claim 1 , wherein a less than stoichiometric quantity of the strong-acid salt as compared to the cation-exchange capacity of the cation-exchange resin is added to the aqueous solution. 17. The method of claim 1 , wherein the producing the scale-control resin is without the use of a strongly alkaline ingredient. 18. A method for precipitating an ionic substance in a liquid comprising contacting a scale-control resin produced by the method recited in claim 1 with the liquid and precipitating the ionic substance in the liquid through an exchange of multivalent cations between the scale-control resin and the liquid, wherein the precipitated ionic substance remains as a stable particle in the liquid. 19. The method of claim 18 further comprising periodically heat-treating the scale-control resin. 20. The method of claim 19 wherein the heat-treating includes rinsing the scale-control resin with hot water. 21. The method of claim 19 wherein an immersion heater and timer are used to perform the periodic heat treatment of the scale-control resin. 22. The method of claim 18 , further comprising removing multivalent ions from the liquid. 23. The method of claim 22 wherein the removal of multivalent ions is downstream from the scale-control resin. 24. The method of claim 22 , wherein the removal of multivalent ions includes reverse osmosis. 25. The method of claim 22 , wherein the removal of multivalent ions includes water softening. 26. The method of claim 22 , further comprising a second removal of multivalent ions from the liquid. 27. The method of claim 26 , wherein approximately 70% of the multivalent cations are precipitated using the scale-control resin prior to the additional removal of multivalent ions from the liquid. 28. A method of controlling scale formation in equipment from a liquid for the equipment, the method comprising the steps of: producing a scale-control resin by combining in an aqueous solution a hydrogen-functionalized weak-acid cation-exchange resin, a weak-acid anion mineral or salt having a multivalent cation, and a strong-acid salt having the same multivalent cation as the weak-acid anion mineral or salt, wherein ions are exchanged between the resin and the weak-acid anion mineral or salt by a catalyzed reaction to produce a scale-control resin that is multivalent cation-functionalized; and contacting the liquid with the scale-control resin to precipitate scale-forming ions or minerals as stable particles that no longer have a significant tendency to attach to downstream surfaces in the equipment. 29. The method of claim 28 , wherein during the step of producing the scale-control resin creating a reaction mixture so that the catalyzed reaction is driven to completion through reaction of hydronium ions with the weak-acid anion mineral or salt that suppresses the hydronium ions in the reaction mixture. 30. The method of claim 29 , further comprising a step of allowing carbon dioxide gas to leave the reaction mixture. 31. The method of claim 28 , wherein during the step of producing a scale-control resin the scale-control resin is converted to a multivalent activated form from an original hydrogen ion form through an initial reaction of hydronium ion with the strong-acid salt and where the weak-acid anion mineral or salt suppresses accumulation of the hydronium ions in the reaction mixture. 32. The method of claim 28 , wherein the producing the scale-control resin is without the use of a strongly alkaline ingredient.

Assignees

Inventors

Classifications

  • C08J3/07Primary

    from polymer solutions · CPC title

  • Modification or after-treatment of ion-exchangers · CPC title

  • in the weakly acidic form · CPC title

  • Macromolecular compounds (B01J39/17 takes precedence) · CPC title

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What does patent US9879120B2 cover?
A method of producing a scale-control resin including combining in an aqueous solution a cation-exchange resin and a weak-acid anion mineral or salt having a multivalent cation to allow ion exchange between the resin and the multivalent cation. The cation-exchange resin may be a weak-acid ion exchange resin. The method may further include adding a strong-acid salt having the same multivalent ca…
Who is the assignee on this patent?
Koslow Evan E, Watts Regulator Co
What technology area does this patent fall under?
Primary CPC classification C08J3/07. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jan 30 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).