Mask and method
US-2024407484-A1 · Dec 12, 2024 · US
US11439721B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11439721-B2 |
| Application number | US-201716466232-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 27, 2017 |
| Priority date | Dec 28, 2016 |
| Publication date | Sep 13, 2022 |
| Grant date | Sep 13, 2022 |
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To provide an aldehyde scavenger and a method for removing aldehydes by using the same, for quickly and continuously capturing aldehydes. An aldehyde scavenger comprising at least one O-substituted hydroxylamine or at least one chemically acceptable salt thereof, is used against an aldehyde generation source.
Opening claim text (preview).
The invention claimed is: 1. A method for removing aldehydes, comprising: bringing an aldehyde scavenger into contact with an aldehyde generation source to remove the aldehydes, wherein the aldehyde scavenger includes at least one O-substituted hydroxylamine, or at least one chemically acceptable salt of the O-substituted hydroxylamine, and the chemically acceptable salt is at least one of a hydrochloride, a hydrobromide, a perchlorate, a silicate, a tetrafluoroborate, a hexafluorophosphate, a sulfate, a nitrate, a phosphate, an acetate, a citrate, a fumarate, a maleate, a trifluoromethanesulfonate, a trifluoroacetate, a benzoate, and a p-toluenesulfonic acid salt, wherein the O-substituted hydroxylamine has formula (1) R 1 —ONH 2 (1) where R 1 is a methyl group or an ethyl group which, at a chemically acceptable position, is substituted by at least a carboxy group and is optionally further substituted by a phenyl group. 2. The method of claim 1 , wherein R 1 is one of a carboxymethyl group, a 1-carboxyethyl group, a 2-carboxyethyl group, an α-carboxy benzyl group, an α-carboxy-phenethyl group, and a β-carboxy-phenethyl group. 3. The method of claim 1 , wherein R 1 is a carboxymethyl group. 4. The method of claim 1 , wherein the aldehyde scavenger is included in an aqueous solution and brought into contact with the aldehyde generation source. 5. The method of claim 2 , wherein the aldehyde scavenger is included in an aqueous solution and brought into contact with the aldehyde generation source. 6. The method of claim 3 , wherein the aldehyde scavenger is included in an aqueous solution and brought into contact with the aldehyde generation source. 7. The method of claim 4 , wherein a content of the aldehyde scavenger included in an aqueous solution is within a range of from 1 to 50 wt %. 8. The method of claim 5 , wherein a content of the aldehyde scavenger included in an aqueous solution is within a range of from 1 to 50 wt %. 9. The method of claim 6 , wherein a content of the aldehyde scavenger included in an aqueous solution is within a range of from 1 to 50 wt %. 10. The method of claim 1 , wherein the aldehyde scavenger is supported on a carrier which is insoluble in water. 11. The method of claim 2 , wherein the aldehyde scavenger is supported on a carrier which is insoluble in water. 12. The method of claim 3 , wherein the aldehyde scavenger is supported on a carrier which is insoluble in water. 13. The method of claim 1 , wherein the aldehyde scavenger is supported on a polymeric carrier or an inorganic carrier which are insoluble in water. 14. The method of claim 2 , wherein the aldehyde scavenger is supported on a polymeric carrier or an inorganic carrier which are insoluble in water. 15. The method of claim 3 , wherein the aldehyde scavenger is supported on a polymeric carrier or an inorganic carrier which are insoluble in water. 16. The method of claim 1 , wherein the aldehyde generation source comprises a plywood or an automobile ceiling material.
Diamines · CPC title
Tertiary amines · CPC title
Inorganic carriers, supports or substrates · CPC title
Volatile organic compounds V.O.C.'s · CPC title
Coated, impregnated or composite adsorbents · CPC title
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