Flame-retardant thermoplastic starch material, flame-retardant thermoplastic starch-based bio-composite, and method for manufacturing the same
US-9127156-B2 · Sep 8, 2015 · US
US9732193B1 · US · B1
| Field | Value |
|---|---|
| Publication number | US-9732193-B1 |
| Application number | US-201615078779-A |
| Country | US |
| Kind code | B1 |
| Filing date | Mar 23, 2016 |
| Priority date | Mar 23, 2016 |
| Publication date | Aug 15, 2017 |
| Grant date | Aug 15, 2017 |
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In an example, a flame-retardant polyhydroxyalkanoate (PHA) phosphonate material has a polymeric backbone that includes a phosphonate linkage between a first PHA material and a second PHA material.
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The invention claimed is: 1. A process comprising: forming a polyhydroxyalkanoate (PHA) material having a terminal carboxylic acid group from a biorenewable aliphatic fatty acid via a bacterial fermentation process; chemically reacting the PHA material with a diol to convert the terminal carboxylic acid group to a terminal hydroxyl group; and chemically reacting the terminal hydroxyl group with a phosphorus-based material to form a flame-retardant PHA phosphonate material. 2. The process of claim 1 , wherein the biorenewable aliphatic fatty acid is formed from a biorenewable plant oil. 3. The process of claim 2 , wherein the biorenewable plant oil includes castor oil, linseed oil, soybean oil, or a combination thereof. 4. The process of claim 1 , wherein the diol includes a biorenewable diol. 5. The process of claim 4 , wherein the biorenewable diol includes ethylene glycol, propylene glycol, butylene glycol, pentylene glycol, or a combination thereof. 6. The process of claim 1 , wherein the phosphorus-based material includes a phosphine oxide. 7. The process of claim 6 , wherein the phosphorus-based material includes dichlorophenylphosphine oxide. 8. The process of claim 1 , wherein the terminal hydroxyl group is chemically reacted with the phosphorus-based material in the presence of a catalyst. 9. The process of claim 8 , wherein the catalyst includes dimethylaminopyridine (DMAP). 10. The process of claim 1 , further comprising forming a polymeric blend that includes the flame-retardant PHA phosphonate material and a second polymeric material. 11. The process of claim 10 , wherein the second polymeric material includes a polylactic acid (PLA) material, a polyurethane material, a polycarbonate material, an acrylonitrile butadiene styrene (ABS) material, a polyester material, a polyether material, or a combination thereof. 12. A flame-retardant polyhydroxyalkanoate (PHA) phosphonate material formed by a process comprising: forming a polyhydroxyalkanoate (PHA) material having a terminal carboxylic acid group from a biorenewable aliphatic fatty acid via a bacterial fermentation process; chemically reacting the PHA material with a diol to convert the terminal carboxylic acid group to a terminal hydroxyl group; and chemically reacting the terminal hydroxyl group with a phosphorus-based material to form a flame-retardant PHA phosphonate material, wherein the phosphorus based material includes a phosphine oxide. 13. The flame retardant PHA phosphonate material of claim 12 , wherein the phosphorus-based material includes dichlorophenylphosphine oxide. 14. The flame-retardant PHA phosphonate material of claim 12 , wherein the diol includes ethylene glycol, propylene glycol, or a combination thereof.
Polyurethanes · CPC title
containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure · CPC title
derived from hydroxy carboxylic acids · CPC title
Compositions of polyethers obtained by reactions forming an ether link in the main chain (of polyacetals C08L59/00; of epoxy resins C08L63/00; of polythioether-ethers C08L81/02; of polyether-sulfones C08L81/06); Compositions of derivatives of such polymers · CPC title
Polyesters derived from hydroxycarboxylic acids, e.g. lactones (C08L67/06 takes precedence) · CPC title
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