Poly(aryl piperidinium) polymers for use as hydroxide exchange membranes and ionomers

Patent metadata

Field	Value
Publication number	US-10290890-B2
Application number	US-201816146887-A
Country	US
Kind code	B2
Filing date	Sep 28, 2018
Priority date	Mar 28, 2016
Publication date	May 14, 2019
Grant date	May 14, 2019

Abstract

Poly(aryl piperidinium) polymers are provided which have an alkaline-stable cation, piperidinium, introduced into a rigid aromatic polymer backbone free of ether bonds. Hydroxide exchange membranes or hydroxide exchange ionomers formed from these polymers exhibit superior chemical stability, hydroxide conductivity, decreased water uptake, good solubility in selected solvents, and improved mechanical properties in an ambient dry state as compared to conventional hydroxide exchange membranes or ionomers. Hydroxide exchange membrane fuel cells comprising the poly(aryl piperidinium) polymers exhibit enhanced performance and durability at relatively high temperatures.

First claim

What is claimed is:

1. A polymer wherein the polymer is one of the following:
(A) the polymer comprises a reaction product of a polymerization mixture comprising
(i) a piperidone monomer having the formula:

or
a 3-oxo-6-azoniaspiro[5.5]undecane salt monomer having the formula:

(ii) an aromatic monomer having the formula:

and
(iii) optionally, a trifluoroacetophenone monomer having the formula:

wherein:
R 1 is alkyl, alkenyl, or alkynyl, and the alkyl, alkenyl or alkynyl are optionally substituted with fluoride;
R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are each independently hydrogen, alkyl, alkenyl, or alkynyl, and the alkyl, alkenyl or alkynyl are optionally substituted with fluoride;
n is 0, 1, 2 or 3; and
X − is an anion; or
(B) the polymer is an anion exchange polymer comprising structural units of Formulae 1A or 2A, 3A, and optionally 4A, wherein the sum of the mole fractions of the structural unit of Formula 1A or 2A and Formulae 4A is equal to the mole fraction of Formulae 3A in the polymer, and the mole ratio of the structural unit of Formula 1A or 2A to the structural unit of Formula 3A is from 0.01 to 1, wherein the structural units of Formulae 1A, 2A, 3A and 4A have the structures:

wherein:
R 10 are each independently alkyl, alkenyl, or alkynyl, and the alkyl, alkenyl or alkynyl are optionally substituted with fluoride;
R 20 , R 30 , R 40 , R 50 , R 60 , R 70 , R 80 , R 90 , R 100 , R 120 , R 130 , R 150 , and R 160 are each independently hydrogen, alkyl, alkenyl, or alkynyl, and the alkyl, alkenyl or alkynyl are optionally substituted with fluoride;
n is 0, 1, 2 or 3; and
X − is an anion; or
(C) the polymer is an hydroxide exchange polymer comprising a poly(aryl piperidinium) backbone free of ether linkages, and having water uptake not more than 60% based on the dry weight of the polymer when immersed in pure water at 95° C., or having hydroxide conductivity in pure water at 95° C. of at least 100 mS/cm; or
(D) the polymer is an hydroxide exchange polymer comprising a poly(aryl piperidinium) backbone wherein the polymer (D) has: and having:
a peak power density of at least 350 mW/cm 2 when the polymer is used as an hydroxide exchange membrane of an hydroxide exchange membrane fuel cell and is loaded at 20% as an hydroxide exchange ionomer in the cathodic and anodic catalyst layers of the fuel cell, the fuel cell having a 50% Pt/C catalyst and catalyst loading of 0.4 mg Pt/cm 2 , and test conditions being hydrogen and oxygen flow rates of 0.6 L/min, back pressure of 0.1 MPa g , and anode and cathode humidifiers at 95° C. and 98° C., respectively; or
a decrease in voltage over 5.5 hours of operation of not more than 20% and an increase in resistance over 5.5 hours of operation of not more than 20% when the polymer is used as an hydroxide exchange membrane of an hydroxide exchange membrane fuel cell and is loaded at 20% as an hydroxide exchange ionomer in the cathodic and anodic catalyst layers of the fuel cell, the fuel cell having a 50% Pt/C catalyst and catalyst loading of 0.4 mg Pt/cm 2 , and test conditions being constant current density of 400 mA/cm 2 , hydrogen and oxygen flow rates of 0.2 L/min, back pressure of 0.05 MPa g , and anode and cathode humidifiers at 95° C. and 98° C., respectively.

2. A polymer wherein either:
(1) the polymer comprises a reaction product of an alkylating agent and the polymer of (A) of claim 1 comprising the reaction product of the polymerization mixture comprising the piperidone monomer; or
(2) the polymer comprises a reaction product of a base and either the polymer of claim 1 or the reaction product of the alkylating agent and the polymer of (A) of claim 1 , the polymer of (A) comprising the reaction product of the polymerization mixture comprising the 3-oxo-6-azoniaspiro[5.5]undecane salt.

3. The polymer of (A) of claim 1 , wherein the piperidone monomer comprises N-methyl-4-piperidone; the 3-oxo-6-azoniaspiro[5.5]undecane salt monomer comprises 3-oxo-6-azoniaspiro[5.5]undecane iodide; the 2,2,2-trifluoroacetophenone monomer comprises 2,2,2-trifluoroacetophenone; and the aromatic monomer comprises biphenyl, para-terphenyl, para-quaterphenyl or benzene.

4. The polymer of (A) of claim 1 , wherein R 1 is alkyl; and R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are each independently hydrogen, or alkyl optionally substituted with fluoride.

5. The polymer of (A) of claim 1 , wherein R 1 is methyl, ethyl, propyl, butyl, pentyl, or hexyl; and R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 14 , R 15 , and R 16 are each independently hydrogen, methyl, ethyl, propyl, butyl, pentyl, or hexyl, or methyl, ethyl, propyl, butyl, pentyl, or hexyl optionally substituted with fluoride.

6. The polymer of (2) of claim 2 , wherein the base comprises a hydroxide-containing base.

7. The polymer of claim 6 , wherein the hydroxide-containing base comprises sodium hydroxide or potassium hydroxide.

8. The polymer of (A) or (B) of claim 1 , wherein X − comprises a halide, BF 4 − , or PF 6 − .

9. The polymer of (C) of claim 1 , wherein the polymer has water uptake not more than 60% based on the dry weight of the polymer when immersed in pure water at 95° C., and has hydroxide conductivity in pure water at 95° C. of at least 100 mS/cm.

10. The polymer of (C) of claim 1 , wherein the polymer is stable to degradation (as evidenced by no change in peak position on its 1 H NMR spectra) when immersed in 1 M potassium hydroxide at 100° C. for 2,000 hours.

11. The polymer of (C) of claim 1 , wherein the polymer is insoluble in pure water and isopropanol at 100° C., but is soluble in a 50/50 mixture by weight of water and isopropanol at 100° C.

12. The polymer of (C) of claim 1 , wherein the polymer has a tensile strength of at least 100 MPa and elongation at break of at least 7%.

13. The polymer of (C) of claim 1 , wherein the polymer has a tensile strength of at least 100 MPa and elongation at break of at least 7%.

14. The polymer of (C) or (D) of claim 1 , wherein the aryl linkages of the poly(aryl piperidinium) backbone free of ether linkages comprise p-phenyl, and the piperidinium linkages comprise hydroxide anions.

15. The polymer of claim 14 , wherein the aryl linkages are derived from biphenyl, para-terphenyl, para-quaterphenyl or benzene monomers.

16. The polymer of (C) or (D) of claim 1 , wherein the piperidinium linkages are derived from N,N-dimethyl-4-piperidinium or 3-oxo-6-azoniaspiro[5.5]undecane salt monomers.

17. The polymer of (C) or (D) of claim 1 , further comprising 2,2,2-trifluoroethylbenzene linkages derived from 2,2,2-trifluoroacetophenone monomer.

18. A method of making the polymer of claim 2 , the method comprising either:
(a) reacting the piperidone monomer, the optional 2,2,2-trifluoroacetophenone monomer, and the aromati

Assignees

• Univ Delaware
• Universty of Delaware

Inventors

• Yan Yushan
• Xu Bingjun
• Wang Junhua
• Zhao Yun

Classifications

• H01M2008/1095

  Fuel cells with polymeric electrolytes · CPC title

• B01D2325/42

  Ion-exchange membranes · CPC title

• Y02P70/56

  Cross-Sectional Technologies · mapped topic

• H01M8/1081

  starting from solutions, dispersions or slurries exclusively of polymers · CPC title

• H01M8/1039

  halogenated, e.g. sulfonated polyvinylidene fluorides · CPC title