Heterocyclic compound, organic light-emitting device including the same, and electronic apparatus including the organic light-emitting device
US-2024373662-A1 · Nov 7, 2024 · US
US9902904B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9902904-B2 |
| Application number | US-201514591303-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 7, 2015 |
| Priority date | Jul 10, 2012 |
| Publication date | Feb 27, 2018 |
| Grant date | Feb 27, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Scale-inhibiting polymers comprising one or more scale-inhibiting units and one or more tagging units, wherein each tagging unit is formed from a compound of Formula I, II, III, or IV, or a salt, hydrate, salt hydrate, stereoisomer, dehydrate or derivative thereof. Scale-inhibiting compositions comprising the scale-inhibiting polymers, processes for determining a concentration of a scale-inhibiting polymer for inhibiting scale formation, and methods for preventing or controlling scale formation in systems comprising fluid circulation with the scale-inhibiting polymers are also disclosed herein.
Opening claim text (preview).
We claim: 1. A scale-inhibiting polymer comprising one or more scale-inhibiting units and one or more tagging units, wherein each tagging unit is formed from a compound of Formula I or II: wherein each R′ is independently R, OR, NRC(S)NR 2 , or NRC(O)NR 2 ; each R is independently H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 6 -C 14 aryl, or C 7 -C 20 aralkyl; and wherein each alkyl or aryl group may be optionally independently substituted with one or more halo, C 1 -C 6 alkyl, or C 1 -C 6 haloalkyl substituents; or a salt, hydrate, salt hydrate, stereoisomer, dehydrate or derivative thereof; wherein the tagging unit is formed from a compound selected from the group consisting of: a hydrochloride, dihydrochloride, sulfate, bisulfate, or gluconate salt of a compound of Formula I or II, and a hydrate thereof; or wherein the one or more scale-inhibiting units comprises maleic acid or maleic anhydride and sodium allyl sulfonate. 2. The polymer of claim 1 , comprising two or more scale-inhibiting units and one or more tagging units. 3. The polymer of claim 1 , wherein R′ is H. 4. The polymer of claim 1 , wherein R′ is O(C 1 -C 6 alkyl). 5. The polymer of claim 1 , wherein R′ is OCH 3 . 6. The polymer of claim 1 , wherein the tagging unit is formed from a compound selected from the group consisting of: a hydrochloride, dihydrochloride, sulfate, bisulfate, or gluconate salt of a compound of Formula I or II, and a hydrate thereof. 7. The polymer of claim 1 , wherein the one or more scale-inhibiting units comprises maleic acid or maleic anhydride and sodium allyl sulfonate. 8. The polymer of claim 1 , wherein the tagging unit is a quinicine monomer: 9. The polymer of claim 1 , wherein the tagging unit is a chinconicine monomer: 10. The polymer of claim 1 , wherein the tagging unit is a quininone monomer: 11. The polymer of claim 1 , wherein the tagging unit is a cinchoninone monomer: 12. The polymer of claim 1 , wherein the one or more tagging units is at a weight percent of total monomers of about 0.01% to about 20%. 13. A process for determining a concentration of a scale-inhibiting polymer for inhibiting scale formation, the process comprising: (a) introducing an effective scale-inhibiting amount of the scale-inhibiting polymer to an aqueous medium to inhibit calcium carbonate, calcium sulfate, barium sulfate, and/or calcium phosphate scale formation; (b) measuring a fluorescence signal of the scale-inhibiting polymer in the aqueous medium; and (c) determining a concentration of the scale-inhibiting polymer based on the fluorescence signal; wherein the scale-inhibiting polymer comprising one or more scale-inhibiting units and one or more tagging units, wherein each tagging unit is formed from a compound of Formula I or II: wherein each R′ is independently R, OR, NRC(S)NR 2 , or NRC(O)NR 2 ; each R is independently H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 6 -C 14 aryl, or C 7 -C 20 aralkyl; and wherein each alkyl or aryl group may be optionally independently substituted with one or more halo, C 1 -C 6 alkyl, or C 1 -C 6 haloalkyl substituents; or a salt, hydrate, salt hydrate, stereoisomer, dehydrate or derivative thereof. 14. A scale-inhibiting composition comprising the scale-inhibiting polymer of claim 1 and a solvent. 15. The composition of claim 14 , further comprising at least one additional tagged polymer having an fluorescence emission signal different from that of the scale-inhibiting polymer. 16. A method for preventing or controlling scale formation in systems comprising fluid circulation, which comprising the steps of: (a) adding to the system or fluid an effective scale-inhibiting amount of a scale-inhibiting polymer; (b) periodically, continually, or continuously measuring the amount of tagging units in the system or fluid; and (c) periodically, continually, or continuously further adding more scale-inhibiting polymer to the system or fluid when the measured amount of tagging units determined by step (b) is below a predetermined value; wherein the scale-inhibiting polymer comprising one or more scale-inhibiting units and one or more tagging units, wherein each tagging unit is formed from a compound of Formula I or II: wherein each R′ is independently R, OR, NRC(S)NR 2 , or NRC(O)NR 2 ; each R is independently H, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 6 -C 14 aryl, or C 7 -C 20 aralkyl; and wherein each alkyl or aryl group may be optionally independently substituted with one or more halo, C 1 -C 6 alkyl, or C 1 -C 6 haloalkyl substituents; or a salt, hydrate, salt hydrate, stereoisomer, dehydrate or derivative thereof. 17. The method of claim 16 , wherein the amount of scale-inhibiting polymer in the system or fluid is less than 35 parts per million. 18. The method of claim 16 , wherein the amount of scale-inhibiting polymer in the system or fluid is less than 0.5 to 35 parts per million. 19. The scale-inhibiting polymer of claim 1 , wherein the polymer has a thermal stability such that when the polymer is kept at a temperature of about 130° C. in water for about one week, there is less than about 10% decrease in emission intensity. 20. The process of claim 13 , wherein scale-inhibiting polymer comprises two or more scale-inhibiting units and one or more tagging units. 21. The process of claim 13 , wherein R′ is H. 22. The process of claim 13 , wherein R′ is O(C 1 -C 6 alkyl). 23. The process of claim 13 , wherein R′ is OCH 3 . 24. The process of claim 13 , wherein the tagging unit is formed from a compound selected from the group consisting of: a hydrochloride, dihydrochloride, sulfate, bisulfate, or gluconate salt of a compound of Formula I or II, and a hydrate thereof. 25. The process of claim 13 , wherein the one or more scale-inhibiting units comprises maleic acid or maleic anhydride and sodium allyl sulfonate. 26. The process of claim 13 , wherein the tagging unit is a quinicine monomer: 27. The process of claim 13 , wherein the tagging unit is a chinconicine monomer: 28. The process of claim 13 , wherein the tagging unit is a quininone monomer: 29. The process of claim 13 , wherein the tagging unit is a cinchoninone monomer:
Sources · CPC title
Water in cooling circuits · CPC title
from quarries or from mining activities · CPC title
containing organic luminescent materials · CPC title
from petrochemical industry (e.g. refineries) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.