Highly basic ionomers and membranes and anion/hydroxide exchange fuel cells comprising the ionomers and membranes
View Patent ↗A family of functionalized polymers is provided capable of forming membranes having exceptional OH − ionic conductivity as well as advantageous mechanical properties, which may be applied to membranes including such polymers for use in, e.g., AEMFC/HEMFC fuel cells. Preferred functional groups include a quaternary phosphonium, and the polymer may specifically be (tris(2,4,6-trimethoxyphenyl) phosphine) 3 functionalized phosphonium polysulfone hydroxide, ECL-PVBC-QPOH, or QPOH based on any of the commercial polumers including polycarbonate (PC), poly(2,6-dimethyl-1,4-phenylene oxide) (PPO), polyetherimine (PEI), poly(ether sulfone) (PES), poly(phenylene sulfoxide) PPS, poly(ether ether ketone) (PEEK), or polybenzimidazole (PBI), polyvinyl chloride (PVC). An ionomer membrane may include polysulfone based TPQPOH, ECL-PVBC-QPOH, and/or PPO.
1. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane comprising:
(a) preparing a mixture of poly(vinylbenzyl chloride) (PVBC) and tris(2,4,6-trirnethoxyphenyl) phosphine (TTMPP) dissolved in an aprotic solvent;
(b) reacting said mixture at greater than 75° C. and for about 24 hours;
(c) introducing a short chain crosslinker into said mixture during said reaction;
(d) casting and curing the reaction mixture at temperature about or less than 30° C. for 24 hours to form a highly basic ionomer membrane; and
(e) heating said membrane to about 135° C. for 3 hours to complete the cross linking reaction with membrane;
(f) wherein said crosslinker is introduced to said mixture to achieve a desired degree of crosslinking (DCL) of said highly basic ionomer membrane; and
(g) wherein the ion exchange capacity of the membrane is about or greater than 1.4 mmol/g.
2. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said PVBC and TTMPP are initially introduced into said mixture to be about equimolar.
3. A method of making crosslinked tri(2,4,6-trimethoxypkenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-Q POH-x%) ionomer membrane as in claim 1 , wherein said crosslinker is an ex-situ cross-linker.
4. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said crosslinker is 4,4′-bis(chloromethyl)-1,1′-biphenyl (CMBP).
5. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said aprotic solvent is nitrogen based.
6. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said aprotic solvent has a boiling point greater than 200° C.
7. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said PVBC reactant polymer initially has a molecular weight of about 55 kda.
8. A method of making crosslinked tri(2,4,6-aimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein the ionic conductivity of said membrane is greater than 48 mS/cm measured at about 20° C.
9. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane has a swelling ratio of about 25 to about 57%.
10. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane has a water up take value of about 60 to 239%.
11. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane has a normalized ion conductivity of about 34.1 to 41.9 mSg/mmol cm.
12. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphoniurn hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein the degree of crosslinking of said membrane measured by 1 H NMR is about 10 to 50%.
13. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in H 2 O at temperature range of 20 to 85° C.
14. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in Methanol at temperature range of 20 to 85° C.
15. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in Ethanol at temperature range of 20 to 85° C.
16. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in Iso-propanol (IPA) at temperature range of 20 to 85° C.
17. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in N,N-Dimethylformamide (DMF) at temperature range of 20 to 85° C.
18. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in Dimethylacetamide (DMAc) at temperature range of 20 to 85° C.
19. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in Dimethyl sulfoxide (DMSO) at temperature range of 20 to 85° C.
20. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is not soluble in N-Methyl-2-pyrrolidone (NMP) at temperature range of 20 to 85° C.
21. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylhenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane is able to sustain up to 300 kPa of fuel cell back pressure without leakage.
22. A method of making crosslinked tri(2,4,6-trimethoxyphenyl) poly(vinylbenzyl chloride) quaternary phosphonium hydroxide (C-PVBC-QPOH-x%) ionomer membrane as in claim 1 , wherein said membrane does not self-crack.