Combined material system for ion exchange membranes and their use in electrochemical processes

Patent metadata

Field	Value
Publication number	US-2017114196-A1
Application number	US-201515318225-A
Country	US
Kind code	A1
Filing date	Jun 12, 2015
Priority date	Jun 12, 2014
Publication date	Apr 27, 2017
Grant date	—

Abstract

Described is a method for producing covalently and/or ionically cross-linked blend membranes from a halomethylated polymer, a polymer comprising tertiary N-basic groups, preferably polybenzimidazole, and, optionally, a polymer comprising cation exchanger groups such as sulfonic acid groups or phosphonic acid groups. The membranes can be tailor-made in respect of the properties thereof and are suitable, for example, for use as cation exchanger membranes or anion exchanger membranes in low-temperature fuel cells or low-temperature electrolysis or in redox flow batteries, or—when doped with proton conductors such as phosphoric acid or phosphonic acid—for use in medium-temperature fuel cells or medium-temperature electrolysis.

First claim

1 . Membrane characterized in that it is consisting of any mixing ratios from the polymeric membrane components:
halomethylated polymer (polymer with CH 2 HaI groups, with HaI═F, Cl, Br, I) polymer with cation exchange groups SO 3 X or PO 3 X 2 (counterion arbitrary, preferred X═H, metal cation, ammonium cation, imidazolium cation, pyridinium cation, etc.) polymer with tertiary N-basic groups and, if appropriate, any chemical compound or a mixture of chemical low- or high-molecular-weight compounds having tertiary N groups.

2 . Membrane according to claim 1 , characterized in that
the halomethylated polymer(s) is (are) selected from arylene main chain polymers with CH 2 -HaI side groups the cation exchange polymer or polymers are selected from sulfonated polymers the tertiary N-basic polymers or polymers are selected from polyimidazoles, polybenzimidazoles, polyimides, polyoxazoles, polyoxadiazoles, polypyridines or aryl polymers having tertiary N-basic functional groups the tertiary N-basic compound(s) is (are) selected from tertiary amines (mono- and diamines) and/or N-monoalkylated and/or N-monoarylated imidazoles, N-monoalkylated or N-monoarylated benzimidazoles, monoalkylated or monoarylated pyrazoles.

3 . Membrane according to claim 1 , characterized in that the polymeric membrane component containing the cation exchange groups is present in molar excess and is thus a cationic conductor (cation exchange membrane CEM).

4 . The membrane as claimed in claim 1 , wherein the polymer membrane component containing the anion exchange groups is present in molar excess and is thus an anionic conductor (anion exchange membrane AEM).

5 . The membrane as claimed in claim 1 , wherein the polymeric membrane component containing N-basic groups is present in molar excess and is thus a proton conductor after doping with phosphoric acid, phosphonic acid, sulfuric acid or other 2- or 3-basic acids which can be used in the temperature range>100° C.

6 . A process for producing membranes as claimed in claim 1 , wherein all polymeric membrane components are mixed and homogenized in a common solvent, a membrane is sprayed, doctored or cast from the resulting solution, the solvent then evaporating at elevated temperatures, the membrane is thereafter detached from the support and finally treated by various methods in order to activate the membrane.

7 . Process according to claim 6 , characterized in that dipolar aprotic solvents such as N, N-dimethylacetamide, N-methylpyrrolidinone, N,N-dimethylformamide, dimethylsulfoxide, N-ethylpyrrolidinone, diphenylsulfone, sulfolane are used as solvents for dissolving the polymers.

8 . The method as claimed in claim 6 , wherein the following post-treatment process is used: (a) soaking in dilute mineral acid at T=room temperature (RT) to 100° C.; (B) soaking in deionized water at room temperature to 100° C.; (C1), if desired, soaking in concentrated phosphoric or phosphonic acid at T=RT up to 150° C. for the preparation of a doped intermediate temperature proton conductor (T=100-220° C.); or (C2), if desired, in dilute alkali metal hydroxide solutions, followed by immersion in demineralized water to produce the OH − form of anion exchange membranes (AEM).

9 . Use of the membranes according to claims 1 to 8 in membrane processes, especially in PEM low temperature fuel cells, PEM medium temperature fuel cells, PEM electrolysis, SO 2 -depolarized electrolysis, redox flow batteries, electrodialysis, diffusion dialysis, nanofiltration, ultrafiltration, reverse osmosis and pressure-retarded osmosis.

10 . Use of the membranes as a component of sensors, electrodes, secondary batteries, fuel cells, alkaline fuel cells or membrane electrode assemblies.

Assignees

• Häring Thomas
• Universität Stuttgart - Inst Für Chemische Verfahrenstechnik
• Univ Stuttgart

Inventors

• Häring Thomas
• Kerres Jochen
• Morandi Carlo

Classifications

• H01M50/426

  Fluorocarbon polymers · CPC title

• H01M50/489

  Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties · CPC title

• H01M50/414

  Synthetic resins, e.g. thermoplastics or thermosetting resins · CPC title

• H01M8/1039

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

• C08J2371/10

  from phenols · CPC title