Halogenated heterocyclic N-halamine coated garbage bags

US10765770B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10765770-B2
Application numberUS-201916380626-A
CountryUS
Kind codeB2
Filing dateApr 10, 2019
Priority dateJan 17, 2017
Publication dateSep 8, 2020
Grant dateSep 8, 2020

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Articles can be provided with odor resistance by applying a dispersion of a halogenated heterocyclic N-halamine in an inert liquid carrier onto the surface of the article and allowing the inert liquid carrier to penetrate into it. The N-halamine accordingly becomes deposited on the surface of the article after the inert liquid carrier penetrates into the article. This method can be used to provide odor resistance to a variety of substrates, including garbage bags. It can also be used to deposit other functional particulates onto the surface of substrates having sufficient porosity to take up the vehicle. For instance, such functional particles can be oxidants that display antimicrobial and/or enzyme inhibitory efficacy or particles having toxin interaction potentials through oxidative degradation or adsorption of toxic substances in air and/or water, such as fluoride uptake by metal oxide microparticles.

First claim

Opening claim text (preview).

What is claimed is: 1. A garbage bag having walls which are comprised of polyethylene, wherein said walls of the garbage bag are coated with particles of a halogenated heterocyclic N-halamine having a particle size which is within the range of about 0.01 μm to 20 μm, and wherein the particles of the halogenated heterocyclic N-halamine are present only on the surface of the walls of the garbage bag; and wherein the walls of said garbage bag have a wall thickness which is within the range of 0.0002 inch to 0.005 inch thick. 2. The garbage bag of claim 1 wherein the halogenated heterocyclic N-halamine is a partially halogenated hydantoin of the structural formula: where X1 and X2 independently represent hydrogen atoms or halogen atoms and R1 and R2 independently represent linear or branched alkyl groups containing from 1 to about 10 carbon atoms. 3. The garbage bag of claim 2 wherein the partially halogenated hydantoin is monochloro-5,5-dimethyl hydantoin. 4. The garbage bag of claim 2 wherein R 1 and R 2 represent an alkyl group containing from 1 to 4 carbon atoms. 5. The garbage bag of claim 2 wherein said halogen atoms are selected from the group consisting of chlorine atoms and bromine atoms. 6. The garbage bag of claim 2 wherein said halogen atoms are chlorine atoms. 7. The garbage bag of claim 2 wherein the partially halogenated hydantoin is selected from the group consisting of Cl 0.5-5,5 -dimethyl hydantoin, Cl 0.9-5,5 -dimethyl hydantoin, Cl 1.1-5,5 -dimethyl hydantoin, Cl 1.05-1.4-5,5 -dimethyl hydantoin, monochloro-5,5-dimethyl hydantoin (MCDMH), Br 0.9.5,5 -dimethyl hydantoin, monobromo-5,5-dimethyl hydantoin (MBDMH), Cl 0.5,5 -methyl-5-ethyl hydantoin, Cl 0.9-5 -methyl-5-ethyl hydantoin, Cl 1.1-5 -methyl-5-ethyl hydantoin, Ch 1.05-1.4-5 -methyl-5-ethyl hydantoin, monochloro-5-methyl-5-ethyl hydantoin, Br 0.9.5 -methyl-5-ethyl hydantoin, and monobromo-5-methyl-5-ethyl hydantoin. 8. The garbage bag of claim 2 wherein the partially halogenated hydantoin is selected from the group consisting of Cl 0.9-5,5 -dimethyl hydantoin, Cl 0.9-5 -methyl-5-ethyl hydantoin, Cl 1.1.5,5 -dimethyl hydantoin, and Cl 1.1-5 -methyl-5-ethyl hydantoin. 9. The garbage bag of claim 1 wherein halogenated heterocyclic N-halamine is selected from the group consisting N-chloro-N-sodiomethylbenzenesulfonamidate trihydrate, N,N-dichloro-4-methylbenzenesulfonamide, N-bromo-N-sodio-4-nitrobenzenesulfonamidate, N,N-dichlorobenzenesulfonamide, N-chloro-N-sodiobenzenesulfonamidate, monochlorosulfamate, dichlorosulfamate, N-chloroimidodisulfonates, sodium N-chloro-N-arylsulfamates, 2,4,6,8-tetrachloro-2,4,6,8-tetrazobicyclooctane-3, 7-dione, sodium trichloroimidometaphosphamate, N-halosulfinylamines, N-halo-N-sodioamidates, chloroisocyanurates, N-halocarbamidates, N-halosulfonamidates, N-chloroimidodisulfonate, N,N-dichloromethylamine, 2-chloro-1,3,5-triazine-2,4,6-triamine, 2,4-dichloro-1,3,5-triazine-2,4,6-triamine, 2,4,6-trichloro-1,3,5-triazine-2,4,6-triamine, 1-chloro-5,5-dimethylhydantoin, 1-bromo-5,5-dimethylhydantoin, 1,3-dibromo-5,5-dimethylhydantoin 1-chloro-3-bromo-5,5-dimethylhydantoin, 1,3-dichloro-5,5-dimethylhydantoin, 1-chloro-4,4,5,5-tetramethylimidazolidin-2-one, 1,3-dichloro-4,4,5,5-tetramethylimidazolidin-2-one, 1-chloro-2,2,5,5-tetramethylimidazolidin-4-one, 1,3-dichloro-2,2,5,5-tetramethylimidazolidin-4-one, 1,3-dichloro-s-triazine-2,4,6-trione, trichloroisocyanuric acid, potassium dichloroisocyanurate, sodium dichloroisocyanurate, potassium dibromoisocyanurate, sodium dibromoisocyanurate, mono to hexachloromelamine, mono to hexabromomelamine, 3-chloro-4,4-dimethyl-2-oxazolidinone, N-chlorosuccinimide, 1-chloropyrrolidine-2,5-dione, 1,3-dichlorotetrahydro quinazoline-2,4-dione, 1,4-dichloro-2,2,5,5-tetrasubstitutedpiperazine-3,6-diones, N-chloro-2,2,6,6-tetramethylpiperidine, N-chloro-4-amino-2,2,6,6-tetramethylpiperidine, polymer-bound N-chloro-N-sodiobenzenesulfonamidates, chlorinated polyacrylamide, brominated polyacrylamide, chlorinated poly(methacrylamide), brominated poly(methacrylamide), poly(N-chloro-2,2,6,6-tetramethyl-4-piperidinyl acrylate), poly(N-chloro-hydantoin-methyl-p-styrene) emulsion, 1-chloro-3-bromoalkyltrimethylammonium-4,4,5,5-tetramethyl imidazolidin-2-one, 1-bromo-3-bromoalkyltrimethylammonium-4,4,5,5-tetramethyl imidazolidin-2-one, 1-chloro-3-bromoalkyltrimethylammonium-2,2,5,5-tetramethyl imidazolidin-4-one, 1-bromo-3-bromoalkyltrimethylammonium-2,2,5,5-tetramethyl imidazolidin-4-one, 2-chloro-4-bromoalkyltrimethylammonium-1,3,5-triazine-2,4,6-triamine, 2-bromo-4-bromoalkyltrimethylammonium-1,3,5-triazine-2,4,6-triamine, 1-chloro-3-bromoalkyltrimethylammonium-5,5-dimethylhydantoin, and 1-bromo-3-bromoalkyltrimethylammonium-5,5-dimethylhydantoin. 10. The garbage bag of claim 1 wherein the particle size is within the range of 0.05 μm to 15 μm. 11. The garbage bag of claim 1 wherein the particle size is within the range of 0.1 μm to 12 μm. 12. The garbage bag of claim 1 wherein the particle size is within the range of 0.1 μm to 10 μm. 13. The garbage bag of claim 1 wherein the particle size is within the range of 0.5 μm to 8 μm. 14. The garbage bag of claim 1 wherein the particle size is within the range of 1 μm to 6 μm. 15. The garbage bag of claim 1 wherein the particle size is within the range of 3 μm to 5 μm. 16. The garbage bag of claim 1 wherein the polyethylene is high density polyethylene. 17. The garbage bag of claim 1 wherein the polyethylene is linear low density polyethylene. 18. A garbage bag having walls which are comprised of polyethylene, wherein said walls of the garbage bag are coated with particles of a halogenated heterocyclic N-halamine having a particle size which is within the range of about 0.01 μm to 20 μm, and wherein the particles of the halogenated heterocyclic N-halamine are present only on the surface of the walls of the garbage bag; and wherein the polyethylene is high density polyethylene. 19. A garbage bag having walls which are comprised of polyethylene, wherein said walls of the garbage bag are coated with particles of a halogenated heterocyclic N-halamine having a particle size which is within the range of about 0.01 μm to 20 μm, and wherein the particles of the halogenated heterocyclic N-halamine are present only on the surface of the walls of the garbage bag; and wherein the polyethylene is linear low density polyethylene.

Assignees

Inventors

Classifications

  • Containers other than laboratory or medical, e.g. bottles or mail · CPC title

  • Odour removal or prevention of malodour · CPC title

  • containing sulfur · CPC title

  • with halogens or compounds of halogens {(C02F1/4674 takes precedence)} · CPC title

  • with means for influencing the odor, e.g. deodorizing substances · CPC title

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What does patent US10765770B2 cover?
Articles can be provided with odor resistance by applying a dispersion of a halogenated heterocyclic N-halamine in an inert liquid carrier onto the surface of the article and allowing the inert liquid carrier to penetrate into it. The N-halamine accordingly becomes deposited on the surface of the article after the inert liquid carrier penetrates into the article. This method can be used to prov…
Who is the assignee on this patent?
Glad Products Co
What technology area does this patent fall under?
Primary CPC classification A61L9/012. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Sep 08 2020 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).