Economical, food-safe extraction of bisphenols
View Patent ↗Methods for extracting bisphenols from polymer substrates are described. The methods include contacting the polymer substrate with an aqueous composition which includes a phase transfer agent, a base and optionally an oxidant, whereby the bisphenol is extracted into the aqueous composition. Suitable phase transfer agents are delineated. Also described are compositions which can be used in the present methods.
1. A method for extracting a bisphenol from a polymer substrate comprising:
contacting the polymer substrate with an aqueous composition comprising a phase transfer agent and a base, whereby the bisphenol is extracted in to the aqueous composition;
wherein:
the phase transfer agent is a quaternary organic ammonium compound of Formula I:
R 1 , R 2 , R 3 , and R 4 may be the same or different and are independently selected from H, C 1 -C 20 alkyl, C 3 -C 8 cycloalkyl, heterocyclyl, C 6 -C 10 aryl and heteroaryl groups, or R 1 and R 2 or R 1 -R 3 together with the nitrogen atom to which they are bound are a part of heterocyclic ring system and at least one of R 1 , R 2 , R 3 , and R 4 is a C 6 -C 10 aryl or heteroaryl group; and
X- represents an anion comprising halide, hydroxide, sulphonate, phosphate, alkylphosphate, dialkylphosphate, borate, alkylborate, nitrite, nitrate, carbonate, bicarbonate, alkanoate, or O,O-dialkyldithiophosphate.
2. The method of claim 1 , wherein the bisphenol is Bisphenol-A.
3. The method of claim 1 , wherein the base comprises an alkali metal hydroxide, an alkali metal oxide, an alkali metal carbonate, an alkali metal bicarbonate, an organic base, a non-nucleophilic base or a quaternary ammonium hydroxide.
4. The method of claim 1 , wherein the base comprises sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate, triethylamine, tributylamine, pyridine, quinoline, lithium diisopropylamide, lithium hexamethyldisilazide, N,N-Dimethylaminopyridine, N,N-Diisopropylethylamine or 1,8-Diazabicycloundec-7-ene.
5. The method of claim 1 , wherein the composition further comprises a peroxide, a hypochlorite, ozone, oxygen, ozone, a nitrogen oxide, a molecular halogen, a nitrate salt, a manganate or permanganate salt, an inorganic peroxide, a halite, a hypohalite, a halogenate or a perhalogenate salt.
6. The method of claim 1 , wherein the composition further comprises oxygen, ozone, chlorine, bromine, or iodine.
7. The method of claim 1 , wherein the composition further comprises a chlorite salt, a hypochlorite salt, a chlorate salt, or a perchlorate salt.
8. The method of claim 1 , further comprising the step of oxidizing the extracted bisphenol.
9. The method of claim 8 , wherein the oxidizing step comprises electrochemical oxidation, enzymatic oxidation or photocatalytic oxidation.
10. The method of claim 1 , wherein the polymer substrate comprises a bisphenol epoxy or a bisphenol polycarbonate.
11. The method of claim 10 , wherein the polymer substrate is a Bisphenol-A epoxy can liner.
12. The method of claim 10 , wherein the polymer substrate is a Bisphenol-A polycarbonate food or beverage container.
13. The method of claim 1 , wherein the pH of the composition is about 9 to about 12.
14. The method of claim 1 , wherein the polymer substrate is contacted with the composition at a temperature of about 0° C. to about 150° C.
15. A method for removing Bisphenol-A from food can linings, the method comprising contacting the can lining with a composition comprising a) cetylpyridinium chloride, b) potassium carbonate or sodium carbonate, and c) sodium hypochlorite.
16. A method for extracting a bisphenol from a polymer substrate comprising:
contacting the polymer substrate with an aqueous composition comprising a phase transfer agent and a base, whereby the bisphenol is extracted in to the aqueous composition;
wherein: the phase transfer agent comprises benzethonium chloride, cetylpyridinium chloride, methylbenzthionium chloride, benzalkonium chloride, cetalkonium chloride, cetrimonium chloride, cetrimide, didecyldimethylammonium chloride, or domiphen bromide.
17. The method of claim 16 , wherein the bisphenol is Bisphenol-A.
18. The method of claim 16 , wherein the base comprises an alkali metal hydroxide, an alkali metal oxide, an alkali metal carbonate, an alkali metal bicarbonate, an organic base, a non-nucleophilic base or a quaternary ammonium hydroxide.
19. The method of claim 16 , wherein the base comprises sodium carbonate, potassium carbonate, cesium carbonate, lithium carbonate, triethylamine, tributylamine, pyridine, quinoline, lithium diisopropylamide, lithium hexamethyldisilazide, N,N-Dimethylaminopyridine, N,N-Diisopropylethylamine or 1,8-Diazabicycloundec-7-ene.
20. The method of claim 16 , wherein the composition further comprises a peroxide, a hypochlorite, ozone, oxygen, ozone, a nitrogen oxide, a molecular halogen, a nitrate salt, a manganate or permanganate salt, an inorganic peroxide, a halite, a hypohalite, a halogenate or a perhalogenate salt.
21. The method of claim 16 , wherein the composition further comprises oxygen, ozone, chlorine, bromine, or iodine.
22. The method of claim 16 , wherein the composition further comprises a chlorite salt, a hypochlorite salt, a chlorate salt, or a perchlorate salt.
23. The method of claim 16 , further comprising the step of oxidizing the extracted bisphenol.
24. The method of claim 23 , wherein the oxidizing step comprises electrochemical oxidation, enzymatic oxidation or photocatalytic oxidation.
25. The method of claim 16 , wherein the polymer substrate comprises a bisphenol epoxy or a bisphenol polycarbonate.
26. The method of claim 16 , wherein the polymer substrate is a Bisphenol-A epoxy can liner.
27. The method of claim 16 , wherein the polymer substrate is a Bisphenol-A polycarbonate food or beverage container.
28. The method of claim 16 wherein the pH of the composition is about 9 to about 12.
29. The method of claim 16 , wherein the polymer substrate is contacted with the composition at a temperature of about 0° C. to about 150° C.