Energy curable sealants
US-9650552-B2 · May 16, 2017 · US
US10160893B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10160893-B2 |
| Application number | US-201615195141-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 28, 2016 |
| Priority date | Jun 28, 2016 |
| Publication date | Dec 25, 2018 |
| Grant date | Dec 25, 2018 |
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The present application is directed to polysulfide sealant formulations, application of such sealants, and methods for reducing the density of polysulfide sealant formulations.
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What is claimed is: 1. A sealant formulation comprising: a polysulfide in an amount ranging from about 75 to about 90 weight %; an acid salt in an amount ranging from about 3 to about 10 weight %; and a bicarbonate in an amount ranging from about 2.5 to about 10 weight %. 2. The sealant formulation of claim 1 , wherein the acid salt comprises at least one of: sodium aluminum sulfate; monocalcium phosphate; delta-gluconolactone; sodium acid pyrophosphate; sodium aluminum phosphate; sodium aluminum pyrophosphate; or potassium bitartrate. 3. The sealant formulation of claim 1 , wherein the bicarbonate comprises at least one of: sodium bicarbonate; potassium bicarbonate; or ammonium bicarbonate. 4. The sealant formulation of claim 1 , wherein the polysulfide comprises at least one of: a polymer comprising one or more disulfide linkages and the polysulfide ranges in molecular weight from about 1100 to about 8000, said polymer comprising a crosslinking density of from about 0.2 to about 5 mol %. 5. The sealant formulation of claim 1 , wherein the polysulfide comprises at least one of: polysulfide polymers made from monomers comprising: 1,3-dichloropropane; 1,3-dibromopropane; 1,2-dichloropropane; 1,4-dichlorobutane; 1,4-dibromobutane; trans-1,4-dibromo-2-butene; 1,3-dichlorobutane; 1,2-dichlorobutane; 1,2-dibromobutane; 2,3-dichlorobutane; 2,3-dibromobutane; 1,5-dichloropentane; 1,5-dibromopentane; 1,4-dichloropentane; 1,4-dibromopentane; 1,3-dichloropentane; 1,2-dichloropentane; 2,3-dichloropentane; 2,4-dichloropentane; 1,6-dichlorohexane; 1,6-dibromohexane; 1,2-dichlorohexane; 1,2-dichlorocyclohexane; 1,2-dichlorocyclohexane cis and trans isomers; 1,3-dichlorocyclohexane; 1,3-dichlorocyclohexane cis and trans isomers; 1,4-dichlorocyclohexane; 1,4-dichlorocyclohexane cis and trans isomers; 1,2-bis(chloromethyl)cyclohexane; 1,2-bis(chloromethyl)cyclohexane cis and trans isomers; 1, I-bis(chloromethyl)cyclo-hexane; 1, I-bis(chloromethyl)cyclohexane cis and trans isomers; 1,4-bis(chloromethyl)cyclohexane; 1,4-bis(chloromethyl)cyclohexane cis and trans isomers; 1,2-bis(chloromethyl)benzene; 1,2,3-trichloropropane; 1,2,3-tribromopropane; ethane,1,1′-thiobis[2-[(2-chloroethyl)thio]-; ethane,1,1′-oxybis[2-chloro]-; sodium sulfide; sodium polysulfide; elemental sulfur or combinations thereof. 6. The sealant formulation of claim 1 comprising: a polysulfide; sodium aluminum sulfate or monocalcium phosphate; and sodium bicarbonate. 7. A cured sealant made from the sealant formulation of claim 1 , wherein the cured sealant has a density ranging from about 0.6 g/cm 3 to about 1.0 g/cm 3 . 8. The sealant formulation of claim 1 , further comprising: an aqueous media in an amount ranging from about 1 to about 5 weight %. 9. A component comprising a cured sealant made from the sealant formulation of claim 8 . 10. A vehicle comprising the component of claim 9 . 11. A method of manufacturing a polysulfide-containing sealant formulation comprising: a polysulfide in an amount ranging from about 75 to about 90 weight %; an acid salt in an amount ranging from about 3 to about 10 weight %; and a bicarbonate in an amount ranging from about 2.5 to about 10 weight %, to form a first mixture. 12. The method of claim 11 , wherein, the step of combining a polysulfide with an acid salt and a bicarbonate to form a first mixture, the acid salt comprising at least one of: sodium aluminum sulfate; monocalcium phosphate; delta-gluconolactone; sodium acid pyrophosphate; sodium aluminum phosphate; sodium aluminum pyrophosphate; or potassium bitartrate. 13. The method of claim 11 , wherein, the step of combining a polysulfide with an acid salt and a bicarbonate to form a first mixture, the bicarbonate comprising at least one of: sodium bicarbonate; potassium bicarbonate; or ammonium bicarbonate. 14. The method of claim 11 , wherein, the step of combining a polysulfide with an acid salt and a bicarbonate to form a first mixture, the polysulfide comprising at least one of: polysulfide polymers made from monomers comprising at least one of: 1,3-dichloropropane; 1,3-dibromopropane; 1,2-dichloropropane; 1,4-dichlorobutane; 1,4-dibromobutane; trans-1,4-dibromo-2-butene; 1,3-dichlorobutane; 1,2-dichlorobutane; 1,2-dibromobutane; 2,3-dichlorobutane; 2,3-dibromobutane; 1,5-dichloropentane; 1,5-dibromopentane; 1,4-dichloropentane; 1,4-dibromopentane; 1,3-dichloropentane; 1,2-dichloropentane; 2,3-dichloropentane; 2,4-dichloropentane; 1,6-dichlorohexane; 1,6-dibromohexane; 1,2-dichlorohexane; 1,2-dichlorocyclohexane; 1,2-dichlorocyclohexane cis and trans isomers; 1,3-dichlorocyclohexane; 1,3-dichlorocyclohexane cis and trans isomers; 1,4-dichlorocyclohexane; 1,4-dichlorocyclohexane cis and trans isomers; 1,2-bis(chloromethyl)cyclohexane; 1,2-bis(chloromethyl)cyclohexane cis and trans isomers; 1,1-bis(chloromethyl)cyclo-hexane; 1,1-bis(chloromethyl)cyclohexane cis and trans isomers; 1,4-bis(chloromethyl)cyclohexane; 1,4-bis(chloromethyl)cyclo-hexane cis and trans isomers; 1,2-bis(chloromethyl)benzene; 1,2,3-trichloropropane; 1,2,3-tribromopropane; ethane,1,1′-thiobis[2-[(2-chloroethyl)thio]-; ethane,1,1′-oxybis[2-chloro]-; sodium sulfide; sodium polysulfide; elemental sulfur or combinations thereof. 15. The method of claim 11 , wherein, in the step of combining a polysulfide with an acid salt and a bicarbonate to form a first mixture, the polysulfide is present in an amount ranging from about 75 to about 90 weight %, the acid salt is present in an amount ranging from about 3 to about 10 weight %, the bicarbonate is present in an amount ranging from about 2.5 to about 10 weight %. 16. The method of claim 11 , further comprising the step of: adding an aqueous media to the first mixture to form a second mixture in an amount of from about 1 to about 5 weight %. 17. The method of claim 11 , after the step of combining a polysulfide with an acid salt and a bicarbonate to form a first mixture, further comprising the step of: mixing the first mixture in a centrifugal mixer at predetermined and varying RPMs for predetermined durations. 18. The method of claim 17 , after the step of adding an aqueous media to the first mixture to form a second mixture, further comprising the step of: mixing the second mixture in a centrifugal mixer at predetermined and varying RPMs for predetermined durations. 19. The method of claim 18 , further comprising the step of: curing the second mixture. 20. The method of claim 19 , wherein, in the step of curing the second mixture, the curing is conducted at a temperature ranging from about 120° F. to about 145° F. for a duration of about 12 hours. 21. The method of claim 19 , wherein, in the step of curing the second mixture, the curing is conducted at a temperature ranging from about 70° F. to about 100° F. 22. The sealant formulation of claim 1 , wherein the sealant formulation cures to form sealant having a density ranging from about 0.6 g/cm 3 to about 1.0 g/cm 3 .
Alkali metal carbonates · CPC title
Polysulfides · CPC title
Polysulfides · CPC title
Polysulfides · CPC title
Polysulfides · CPC title
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