Fragrant oil encapsulation
US-2015210965-A1 · Jul 30, 2015 · US
US10842148B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10842148-B2 |
| Application number | US-201716310631-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 30, 2017 |
| Priority date | Jun 30, 2016 |
| Publication date | Nov 24, 2020 |
| Grant date | Nov 24, 2020 |
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.
Methods and formulations for antimicrobial and anti-biofouling coating comprising: a hollow round colloidal structure, comprising: an active polymer shell; and an active or inert core; wherein the active polymer shell comprises one and more polymers with antimicrobial and anti-biofouling activities selected from the group consisting of polyethylenimine (PEI), functionalized chitosan (CHI), polyquaternium, poly(diallyldimethylammonium chloride) (PDDA) and polyhexamethylene biguanide (PHMD); wherein the active or inert core contains one and more disinfectants, biocides, fragrances or inert solvent; and wherein the hollow round colloidal structure is stable for at least 3 months.
Opening claim text (preview).
What is claimed is: 1. An antimicrobial and anti-biofouling coating formulation, comprising: a hollow round colloidal structure, comprising: an active polymer shell; and an active or inert core, wherein the active polymer shell comprises polymers with antimicrobial and anti-biofouling activities, including polyethylenimine (PEI), poly(diallyldimethylammonium chloride) (PDDA) and polyhexamethylene biguanide (PHMB), wherein the core is active and contains one or more disinfectants, biocides and fragrances, wherein the core is inert and contains water or an inert solvent, wherein the hollow round colloidal structure is stable for at least 3 months, and wherein a size of the hollow round colloidal structure is between 0.5 μm and 20 μm, the size being controlled by adjusting molecular weights and compositional ratios of the polymers. 2. The coating formulation according to claim 1 , wherein the polymers are present in a concentration of 0.5-100 wt % of the polymer shell. 3. The coating formulation according to claim 2 , wherein the polymers are present in a concentration of 10-20 wt % of the polymer shell. 4. The coating formulation according to claim 1 , wherein the core is an active core comprising one or more biocides selected from the group consisting of essential oil, polyol and aldehyde. 5. The coating formulation according to 4 , wherein the biocide is an essential oil and the essential oil is thyme oil. 6. The coating formulation according to claim 4 , wherein the biocide is a polyol and the polyol is farnesol. 7. The coating formulation according to claim 4 , wherein the biocide is an aldehyde and the aldehyde is cinnamaldehyde. 8. The coating formulation according to claim 4 , wherein the one or more biocides comprises an essential oil and the essential oil is thyme oil, a polyol and the polyol is farnesol and an aldehyde and the aldehyde is cinnamaldehyde. 9. The coating formulation according to claim 1 , wherein the active polymer shell comprises 0.0001-5% (w/v) of the PEI, having a mw of 1,200-60,000 g/mol, 0.05-3% (w/v) of the PHMB, having a mw of 2,000-2,600 g/mol, and 0.01-20% (w/v) of the PDDA, having a mw of 250,000-350,000 g/mol, and wherein the active core contains 0.01-1.5% (w/v) of thyme oil, 0.01-1.5% (w/v) of farnesol, and 0.05-1.5% (w/v) of cinnamaldehyde. 10. The coating formulation of claim 9 , wherein the coating formulation further comprises: 0.01-20% (w/v) of polyvinyl alcohol having a mw 31,000-186,000 g/mol; 0.01-20% (w/v) of PEGMA having a Mn of 500; and 0.01-20% (w/v) of MPEGMA having a Mn of 950. 11. The coating formulation of claim 1 , wherein the coating formulation further comprises stabilizers. 12. A method of producing antimicrobial and anti-biofouling coating for application to nonporous surfaces, porous membranes or porous materials, comprising: preparing an antimicrobial and anti-fouling formulation by the steps of: preparing an aqueous solution containing one or more active polymers, wherein the one or more active polymers are selected from the group consisting of polyquaternium, poly(diallyldimethylammonium chloride) (PDDA) and polyhexamethylene biguanide (PHMB); adding biocides or solvents into the aqueous solution of active polymers; preparing an emulsion having a hollow round colloidal structure comprising adding a stabilizer mixture containing one and more surfactants to the biocides or solvents and solution of active polymers to form the antimicrobial and anti-biofouling formulation; and preparing the antimicrobial and anti-biofouling coating from the antimicrobial and anti-biofouling formulation; and applying the antimicrobial and anti-biofouling coating on nonporous surfaces, porous membranes or porous materials. 13. The method according to claim 12 , wherein the nonporous surfaces are stainless steel, glass and polyvinyl chloride surfaces. 14. The method according to claim 12 , wherein the porous membranes are selected from the group consisting of reverse osmosis membranes, nanofiltration membranes, ultrafiltration membranes, microfiltration membranes and high-efficiency particulate air filters. 15. The method according to claim 12 , wherein the porous materials are nonwoven and woven fabric materials. 16. The method according to claim 12 , wherein the surfactants are polyvinyl alcohol and polyethylene glycol. 17. The method according to claim 12 , wherein applying the antimicrobial and anti-biofouling coating comprises at least one of wiping, brushing, casting, dip-coating, wash-coating, spin-coating, spray-coating and layer-by-layer coating the antimicrobial and anti-biofouling formulation onto nonporous surfaces, porous membranes or porous materials. 18. The method according to claim 12 , wherein applying the antimicrobial and anti-biofouling coating comprises incorporating the antimicrobial and anti-biofouling formulation into a paint or an epoxy resin for direct application on nonporous surfaces, porous membranes or porous materials. 19. The method according to claim 12 , wherein applying the antimicrobial and anti-biofouling coating on porous membranes further comprises rejecting round colloids on the surfaces of porous membranes by a further filtration method thereby forming a reversible coating. 20. An antimicrobial and anti-biofouling coating formulation, comprising: a hollow round colloidal structure, comprising: an active polymer shell; and an active core, wherein the core contains one or more disinfectants, biocides and fragrances, wherein the active polymer shell comprises 0.0001-5% (w/v) polyethylenimine (PEI) having a mw of 1,200-60,000 g/mol, 0.05-3% (w/v) polyhexamethylene biguanide (PHMB) having a mw of 2,000-2,600 g/mol, and 0.01-20% (w/v) of poly(diallyldimethylammonium chloride) (PDDA) having a mw of 250,000-350,000 g/mol, and wherein the active core contains 0.01-1.5% (w/v) of thyme oil, 0.01-1.5% (w/v) of farnesol, 0.05-1.5% (w/v) of cinnamaldehyde, wherein the core is active and contains one or more disinfectants, biocides and fragrances, wherein the hollow round colloidal structure is stable for at least 3 months.
by addition of a layer chemically bonded to the membrane · CPC title
Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic · CPC title
Microcapsules {or nanocapsules} · CPC title
Alcohols; Metal alcoholates (D06M13/11 takes precedence) · CPC title
Biocides, pest repellants or attractants, or plant growth regulators, containing compounds containing the group [IMAGE cpc-sch-A01N-0948.gif], wherein m+n>=1, both X together may also mean —Y— or a direct carbon-to-carbon bond, and the carbon atoms marked with an asterisk are not part of any ring system other than that which may be formed by the atoms X, the carbon atoms in square brackets being part of any acyclic or cyclic structure, or the group [IMAGE cpc-sch-A01N-0949.gif], wherein A means a carbon atom or Y, n>=0, and not more than one of these carbon atoms being a member of the same ring system, e.g. juvenile insect hormones or mimics thereof (containing hydrocarbons A01N27/00) · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.