CA3066028A1 - Crosslinked highly stable anion-exchange blend membranes with polyethyleneglycols as the hydrophilic membrane phase - Google Patents

Crosslinked highly stable anion-exchange blend membranes with polyethyleneglycols as the hydrophilic membrane phase Download PDF

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CA3066028A1
CA3066028A1 CA3066028A CA3066028A CA3066028A1 CA 3066028 A1 CA3066028 A1 CA 3066028A1 CA 3066028 A CA3066028 A CA 3066028A CA 3066028 A CA3066028 A CA 3066028A CA 3066028 A1 CA3066028 A1 CA 3066028A1
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Jochen Kerres
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    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/20Manufacture of shaped structures of ion-exchange resins
    • C08J5/22Films, membranes or diaphragms
    • C08J5/2206Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
    • C08J5/2218Synthetic macromolecular compounds
    • C08J5/2268Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds, and by reactions not involving this type of bond
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0002Organic membrane manufacture
    • B01D67/0006Organic membrane manufacture by chemical reactions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/02Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/12Composite membranes; Ultra-thin membranes
    • B01D69/125In situ manufacturing by polymerisation, polycondensation, cross-linking or chemical reaction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2323/00Details relating to membrane preparation
    • B01D2323/30Cross-linking
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    • C08J2327/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
    • C08J2327/02Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
    • C08J2327/04Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
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    • C08J2471/00Characterised by the use of polyethers obtained by reactions forming an ether link in the main chain; Derivatives of such polymers
    • C08J2471/02Polyalkylene oxides
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    • C08J2479/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2461/00 - C08J2477/00
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    • C08J2481/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen, or carbon only; Polysulfones; Derivatives of such polymers
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Abstract

(12) NACH DEM VERTRAG CIBER DIE INTERNATIONALE ZUSAMMENARBEIT AUF DEM GEBIET
DES
PATENTWESENS (PCT) VERÖFFENTLICHTE INTERNATIONALE ANMELDUNG
(19) Weltorganisation für geistiges Eigentum Internationales Miro (43) Internationales Verdffentlichungsdatum ( 1 ) Internationale Vertiffentlichungsnummer 28. Dezember 2017 (28.12.2017) WIPO I PCT WO 2017/220065 Al (51) Internationale Patentklassifikation: IVERSITAT STUTTGART [DE/DE];
Keplerstrasse 7, C08J 3/24 (2006.01) HOIM 2/16 (2006.01) 70174 Stuttgart (DE). HARING, Thomas [DE/DE]; Fei-CO8J 5/22 (2006.01) HOIM 8/1018 (2016.01) genweg 15, 70619 Stuttgart (DE).
HOIM 2/14 (2006.01) (72) Erfinder; und (21) Internationales Aktenzeichen:
PCT/DE2017/000179 (71) Anmelder: KERRES, Jochen [DE/DE]; Albstrasse 10, 73760 Ostfildern (DE).
(22) Internationales Anmeldedatum:
22. Juni 2017 (22.06.2017) (81) Bestimmungsstaaten (soweit nicht anders angegeben..fiir jede vetfligbare nationale Schutzrechtsart): AE, AG, AL, (25) Einreichungssprache: Deutsch AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (26) Veröffentlichungssprache: Deutsch BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DJ, DK, DM, DO, DZ, EC, BE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (30) Angaben zur Priorität:
HN, HR, HU, Ill, IL, IN, IR, IS, JO, JP KE, KG, KH, KN, 2016 007 815.4 KP, KR, KW, KZ, LA, LC, LK, LR, LS, LU, LY, MA, MI), 22. Juni 2016 (22.06.2016) DE
ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, (71) Anmelder: BETWEEN LIZENZ GMBH [DE/DE]; c/o NZ, OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, Thomas Haring, Feigenweg 15, 70619 Stuttgart (DE). UN-- (54) Title: CROSS-LINKED HIGH STABLE ANION EXCHANGE BLEND MEMBRANES WITH
POLYETHYLENEGLYCOLS
= AS HYDROPHILIC MEMBRANE PHASE
II=1====
(54) Bezeichnung: VERNETZTE HOCHSTABILE ANIONENAUSTAUSCHERBLENDMEMBRANEN MIT
POLYETHYLENGLYCOLEN ALS HYDROPHILER MEMBRANPHASE

X
120 _______ X
M1K2176-1mKOH_20d 100 __ MR2176-1mKOH 30d X
A MJK2176-before KOH
X
80 __ x M1K2176-1mKOH 10d X
0 60 ____________________________________ X
=-===_ 6, 40 X _____ A
=MEM
20 6 ___________________________________ T /* C
Abbildung 2 el (57) Abstract: The invention relates to: - anion exchange blend membranes consisting the following blend components: - a halomethy-lated polymer (a polymer with -(CH2)x-CH2-Ha1 groups, Hal=F, Cl, Br, I; :=1-12), which is quaternised with a tertiary or a ed/n-arylated irnidazole, an N-alkylated/N-arylated benzirnidazole or an N-alkylated/N-arylated pyrazol to forrn an anion exchanger so polymer. - an inert matrix polymer in which the anion exchange polymer is embedded and which is optionally covalently crosslinked eqi with the halomethylated precursor of the anion exchanger polymer, - a polyethyleneglycol with epoxide or halomethyl terminal groups 0., which are anchored by reacting with N-II-groups of the base matrix polymer using convalent cross-linking - optionally an acidic CA 3066028 2019-12-23 [Fortsetzung auf der nächsten Seite]

SA, SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, ZW.
(84) Bestimmungsstaaten (soweit nicht anders angegeben, fiir jede verfigbare regionale Schutzrechtsart): ARIPO (BW, GH, GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), eurasisches (AM, AZ, BY, KG, KZ, RU, TJ, TM), europäisches (AL, AT, BE, BG, CH, CY, CZ, DE, DK, EL, ES, F1, FR, GB, (jR, HR, HU, IE, IS, IT, LT, LU, LV, MC, MK, MT, NL, NO, PL, PT, RO, RS, SE, SI, SK, SM, TR), OAPI (BF, BJ, CF, CG, CI, CM, GA, GN, GQ, GW, KM, ML, MR, NE, SN, TD, TG).
Erkliirungen gemä Regel 4.17:
¨ hinsichtlich der Berechtigung des Anmelders, die Prioritiit einer fruheren Anmeldung zu beanspruchen (Regel 4.17 Zijfer iii) Veröffen ¨ mit internationalem Recherchenbericht (Artikel 21 Absatz 3) ¨ vor Ablauf der fdr Anderungen der Anspriiche geltenden Frist; verVentlichung wird wiederholt, falls iinderungen eingehen (Regel 48 Absatz 2 Buchstabe h) polymer which forms with the anion-exchanger polymer an ionic cross-linking (negative bound ions of the acidic polymer forming ionic cross-linking positions relative to the positive cations of the anion-exchanger polymer) - optionally a sulphonated polymer (polymer with sulphate groups -S02Me, Me= any cation), which forms with the halomethyl groups of the halomethylated polymer convalent crosslinking bridges with sultinate S-alkylation. The invention also relates to a method for producing said membranes, to the use of said membranes in electrochemical energy conversion processes (e.g. Redox-flow batteries and other flow batteries, PEM-electrolyses, membrane fuel cells), and in other membrane methods (e.g. electrodialysis, diffusion dialysis).
(57) Zusammenfassung: Die Erfmdung umfasst: - Anionenaustauscherblendmembranen aus folgenden Blendkomponenten: - Ein ha-lomethyliertes Polymer (ein Polymer mit -(CH2)x-CH2-Ha1-Gruppen, Hal=F, Cl, Br, I; x=0-12), das mit einem tertiären oder einem N-alkylierten/N-arylierten Imidazol, einem N-alkylierten/N-arylierten Benzimidazol oder einem N-alkylierten/N-arylierten Pyrazol zu einem Anionenaustauscherpolymer quatemisiert wird. - Ein inertes Matrixpolymer, in das das Anionenaustauscherpolymer eingebettet ist und das ggf. mit der halomethylierten Vorstufe des Anionenaustauscherpolymers kovalent vemetzt wird. - Ein Polyethylenglycol mit Epoxid- oder Halomethylendgruppen, die durch Reaktion mit basischen N-H-Gruppen des basischen Matrixpolyrners unter ko-valenter Vemetzung verankert werden - Optional ein saures Polymer, das mit dem Anionenaustauscherpolymer ionische Vemetzung ausbildet (negative Festionen des sauren Polymers bilden ionische Vernetzungsstellen zu den positiven Kationen des Anionenaustau-scherpolymers aus) - Optional ein sulfmiertes Polymer (Polymer mit Sullinatgruppen -S02Me, Me=beliebiges Kation), das mit den Halomethylgruppen des halomethylierten Polymers unter Sulfinat-S-Alkylierung kovalente Vemetzungsbriicken ausbildet - Verfahren zur Herstellung dieser Membranen - Anwendung dieser Membranen in elektrochemischen Energiewandelprozessen (z. B. Redox-flow-Batterien und andere Flow-Batterien, PEM-Elektrolysen, Membranbrennstoffzellen, und in sonstigen Membranverfahren (z. B. Elek-trodialyse, Diffusionsdialyse).

Description

Title: Crosslinked highly stable anion-exchange blend membranes with polyethylene glycols as the hydrophilic membrane phase Summary The invention comprises:
anion-exchange blend membranes from the following blend components:
- A halomethylated polymer (a polymer having ¨(CH2)x-CH2-Hal which is tertiary or N-alkylated / N-arylated lmidazole, an N-alkylated / N-arylated benzimidazole or an N-alkylated / N-arylated pyrazole is quaternized to an anion exchange polymer.
- An inert matrix polymer in which the anion exchange polymer is embedded and which is optionally covalently crosslinked with the halomethylated precursor of the anion exchange polymer.
- A polyethylene glycol having epoxide or halomethyl end groups anchored by reaction with basic N-H groups of the basic matrix polymer covalently crosslinked - Optionally an acidic polymer which forms ionic crosslinking with the anion exchange polymer (negative fixed acid ions form ionic crosslink sites to the positive cation of the anion exchange polymer) - Optionally a sulfinated polymer (polymer having sulfinate groups ¨502Me, Me = any cation) which forms covalent crosslinking bridges with the halomethyl groups of the halomethylated polymer under sulfinate S-alkylation - Process for the preparation of these membranes - Use of these membranes in electrochemical energy conversion processes (eg redox-flow batteries and other flow batteries, PEM electrolyses, membrane fuel cells, and in other membrane processes (eg electrodialysis, diffusion dialysis).

Title: Crosslinked highly stable anion-exchange blend membranes with polyethylene glycols as the hydrophilic membrane phase State of the art Over the past few decades, researchers' interest in anion exchange membranes (AEMs) for use in electrochemical conversion processes has greatly increased. Possible fields of application of AEMs are alkaline polymer electrolyte fuel cells (APEFCs) [1,2,3,4,5], alkaline polymer electrolyte electrolysis (APEE) [6], redox flow batteries (RFBs) [7,8,9], reverse electrodialysis (RED) [10,11] and bioelectrochemical systems, including microbial fuel cells (MFCs) [12,13] and enzymatic fuel cells [14]. In addition, anion exchange membranes are used in electrodialysis (ED) [15,16,17] and in Donnan [18] or diffusion dialysis [19] (DD). A
major advantage of using AEM in electrochemical conversion processes such as fuel cells or electrolysis is that when using AEMs for the electrocatalytic reactions at the electrodes no precious metal catalysts consisting of platinum group metals (PGM) are required, thus containing AEM Membrane electrode assemblies (MEAs) are significantly less expensive than cation exchange membrane (CEM) containing MEAs. AEMs have the following major drawbacks compared to CEMs:
(1) The ionic conductivity of most AEM types is significantly lower than that of CEMs of comparable ion exchange capacity (IEC), in part because most of the AEMs have a hydrocarbon backbone that is significantly less hydrophobic than the perfluorinated one, for example the polymer backbone of the perfluorinated membranes of the Nafion type, so that in the AEM it comes to a lower separation between ionic groups and polymer backbone, which leads to lower ionic conductivity because of the then lower local density of the anion exchange groups, especially in most AEM types, the solid cations are attached to the polymer backbone via a CH2 bridge [20].
(2) In particular, when the AEMs are exchanged with the OH- ion, for example when used in APEFC or APEE, their chemical stability is limited, since the OH- counterion of the anion exchange group can degrade the positively charged solid ion itself [21] or the polymer main chain [22].

The global efforts in this research and development segment are aimed at minimizing these disadvantages of AEMs and thus improving their properties. As starting polymers for AEM
often polymers are used which contain aromatic groups, such as polystyrene, polyphenylene ethers or other aromatic polyethers such as polyethersulfones, polyether ketones etc., which may be substituted with methyl groups. The first step in the preparation of AEM is the synthesis of a polymer with halomethyl side groups. Halomethylation is achieved by (1) chloro- or bromomethylation with hydrogen halide, formaldehyde, and a Lewis acid such as ZnCl2 or AlC13 (Blanc reaction [23,24]), or (2) bromination of the CH3 pendant group of aromatic polymers with N-bromo-succinimide (NBS) by the Wohl-Ziegler bromination reaction [25]. The Blanc reaction is associated with the appearance of the highly carcinogenic by-product bis (chloromethyl) ether. For this reason, the Wohl-Ziegler reaction is now preferably used in the production of halomethylated aromatic polymers.
Literature examples for the preparation of bromomethylated aromatic polymers by the Wohl-Ziegler reaction are the bromomethylation of polyphenylene oxide [26] or the bromomethylation of a methylated polyethersulfone [27]. Conversion of the CH2Hal group (Hal = Cl, Br) to an anion exchange group is achieved by reaction with a tertiary amine such as trimethylamine [24], pyridine [28], pentamethylguanidine [29] or an N-alkylated imidazole [30].
One way to increase the conductivity of AEM is to increase the separation between polymer backbone and ion group phase in the AEM to obtain a larger local density of ion-conducting groups. Phase-segregated AEMs having improved ionic conductivity are obtainable by the preparation of linear block copolymers of hydrophobic and ionic blocks [31] or by graft copolymers having an anion exchange group-containing graft side chain [32]
(Example:
grafting of vinylbenzyl chloride side chains to e--irradiated ETFE, and quaternization of the chloromethylated side chains with trimethylamine [33]).
In order to achieve an improvement in the chemical stability of AEM, the combination of anion exchange group and polymer main chain must always be investigated, since the stability of the anion exchange group always depends on the polymer main chain. Thus, it could be shown for polystyrene (P5t) substituted with the solid cation benzyltrimethylammonium that in alkaline medium (0.6M KOH, 80 C) the solid cation is somewhat more stable than if PPO is substituted with the same group and much more stable than if pendent to polyphenylene ether sulfone (PES ) [22]. It is not easy to predict which polymer backbone is more stable, as can be seen in the above example, since all three polymers PSt, PPO and PES contain electron-rich aromatic groups linked together by ether groups in both PPO and PES.
It has been found, however, that apparently by steric shielding of the anion exchange groups of AEM, in particular their alkali stability can be significantly improved, since then the nucleophilic attack of the OH- counterions on the quaternary ammonium group is difficult. In a study by Holdcroft et al, two different polybenzimidazolium (PB1m+) AEMs were tested for their stability in the alkaline medium [34]. One of the PB1m+-AEMs had methyl groups on the aromatic adjacent to the dimethylbenzimidazolium cation, the others did not.
While the sterically hindered PB1m+-AEM showed a very high stability in 2M KOH, the sterically unhindered PBIm+-AEM was degraded very rapidly. The very high stability of the sterically hindered PB1m+-AEM was explained by the authors of this study as follows: at the sterically hindered PB1m+-AEM, the OH- group can not attack the imidazolium ring, while at the non-hindered PB1m+-AEM the OH- can attack the imidazolium ring under ring opening [35].
Herring et al. synthesized sterically highly-hindered PPO-AEM functionalized with 1,4,5-trimethy1-2- (2,4,6-trimethoxyphenyl) -imidazolium anion exchange groups, which were also characterized by excellent alkaline stability (no decrease in ion exchange capacity after 25 hours storage in 1M KOH at 80 C) [36]. In contrast, dimethylimidazolium-modified PPO
showed a large decrease in ion-exchange capacity (approximately 50% decrease in 2M KOH
at 60 C after 9 days) [37]. The experimental findings can be summarized in that the steric shielding of the anion exchange groups is one way to increase the chemical stability of AEM.
Other strategies for reducing the chemical degradation of AEM are:
(1) Search for alternative solid cations (2) chemical and / or physical crosslinking
(3) embedding the anion exchange polymer in an inert matrix polymer.
As alternative cations to the most commonly used trialkylammonium groups are the already mentioned pentamethylguanidinium groups (PMG) come into consideration.
However, it has been found that the PMG cations are chemically stable only when they are resonance-stabilized (ie, the positive charge of the PMG cation is delocalized), which is the case when attached to an aromatic (possibly electron-deficient) moiety, as Kim et al.
could show [38,39]. Another example of a sterically hindered chemically stabilized cationic functional group is the tris (2,4,6-trimethoxyphenyl) phosphonium cation [40], which was attached to polyvinylbenzyl chloride graft chains and after 75 hours of storage in 1N NaOH
at 60 C had no degradation. In a work by Zha et al., for example, a positively charged bis (terpyridine) ruthenium (II) complex was attached to a norbornene polymer [41]. The AEM thus prepared showed excellent stability in an alkaline environment: incorporation of the polymer in 1N
NaOH at room temperature showed no degradation even after half a year.
Another way of stabilizing AEM is to cross-link them. Thus, in a work by He et al. PPO-based AEMs were synthesized, which were cross-linked in a multi-step process with tertiary diamines and vinylbenzyl chloride under quaternization, resulting in mechanically very robust covalently cross-linked AEMs [42]. In a study by Cheng et al. For example, chloromethylated PSU was cross-linked with a novel N-basic difunctional reagent, guanimididazole, under quaternization. These new crosslinked polymers showed better alkali stability than corresponding AEMs quaternized without crosslinking with methylimidazole [43].
In our group, bromomethylated PPO embedded in the matrix polymer PVDF was quaternized with the diamine DABCO and with 1,4-diiodobutane to mechanically and chemically covalently crosslinked AEM. Even after 10 days of incorporation in 1N KOH at 90 C no degradation of IEC and conductivity was observed. Moreover the membranes showed good performance in direct methanol fuel cells (DMFC) (4M Me0H and 5M KOH) [44]. In another study, PB100 (manufacturer: Fuma-Tech) methylated by a new non-carcinogenic reagent was blended with sulfonated PSU and covalently crosslinked under quaternization and alkylation using DABCO and 1,4-diiodobutane [45]. These AEM were tested in a DMFC using non-platinum catalysts (anode: 6% Pd / Ce0 2 / C, cathode: 4% FeCo / C) and gave a good performance at 80 C (anode feed 4M Me0H + 5M KOH) comparable to a commercial Tokuyama-AEM (maximum power density 120 mW/cm2). Another study of our work group comprises the synthesis of ionically and covalently cross-linked AEM blends of bromomethylated PPO or a bromomethylated and partially fluorinated arylene main chain polymer and a partially fluorinated PBI (F6PBI) as a mechanically and chemically stable matrix and a sulfonated polyethersulfone sPPSU [46] added in deficit. The halomethylated blend component was quaternized with N-methylmorpholine (NMM) to the anion exchange group [47]. The interaction between the sulphonate groups of the sulphonated polymer and the basic N-methylmorpholinium cations resulted in the formation of ionic crosslinks, which led to an improvement in the mechanical and chemical stability of the AEM blend.
The alkali stability of the membranes was examined in 1M KOH at 90 C over a period of 10 days as compared to a commercial Tokemama AEM (A201). The most stable of the produced AEM
blends lost about 40% of their original CI- conductivity while the commercial A201 only had 21% of the original conductivity after that period. Similar AEM blends were synthesized in another work: brominated PPO was blended with PB100 or F6PBI as the matrix polymer, and to the blend of brominated PPO and F6PBI, sPPSU was further added as an ionic crosslinker.
The quaternization of the bromomethylated PPO to generate the anion exchange groups was carried out with 1-methylimidazole or 1-ethyl-3-methylimidazole [41.
Examination of the alkali stability (1M KOH, 90 C, 10 days) revealed a conductivity of 69% of the original conductivity for the blend membrane of 1-methylimidazole-quaternized PPO, F6PBI and sPPSU as ionic crosslinker after the stability test, while the blends from PPO
quaternized with the two imidazoles and PB100 had a residual ionic conductivity between 31 and 43% of the original value.
In addition to chemical stability, the achievement of the highest possible selectivities for certain anions is an important research and development topic of AEM, when used in electrodialysis or diffusion dialysis. Sata et al. investigated the dependence of the permeation of different anions on the hydrophobicity of the AEM functional groups. The hydrophobicity of the AEM functional groups has been systematically increased by increasing the length of the quaternary ammonium ion-bonded alkyl chains of trimethylbenzylammonium, triethylbenzylammonium, tri-n-propylbenzylammoniurn, tri-n-butylbenzylammonium, and tri-n-pentylbenzylammonium. It has been found that as the hydrophobicity of the ammonium group increases, the relative transport of large hydrate shell anions, such as sulfate or fluoride ions, to anions with smaller hydration shells, such as chloride or nitrate, significantly decreases [49,50]. In another study, in which AEMs were hydrophilized by impregnation with ethylene glycols of different molecular masses, a marked increase in membrane permselectivity was observed for anions with large hydration shells, such as sulfate or fluoride [51]. In a work by Hickner et al, AEMs were synthesized consisting of rigid / flexible semi-interpenetrating networks of triethylamine-quaternized PPO and a polyethylene glycol network. It was found that this AEM has a high ionic conductivity (crow- up to 80 mS / cm) and a high alkali stability (degradation of ionic conductivity between 25 and 30% within 30 days of storage in 1M NaOH at 80 C) [52]. In another work, polyethylene glycols were grafted onto chloromethylated SEBS
polymers, and the resulting copolymers were then quaternized with trimethylamine. The resulting AEMs showed very high mechanical and chemical stabilities in 2.5M KOH at 60 C
(increasing the ionic conductivity during storage in the KOH from 20 to 24 mS / cm) and high ionic conductivities (a0H- up to 52 mS / cm) [53].
The above-mentioned own studies have shown that covalent or ionic crosslinking and / or embedding of the anion exchange polymer in a chemically stable polymer matrix is a viable way to obtain chemically and mechanically stable AEMs. This work and work from the scientific community on AEMs with sterically hindered cationic groups as well as AEMs with additional hydrophilic phase are the starting point for the novel anion-exchange blend membranes described in this invention.

Description of the invention Surprisingly, it has been found that in anion-exchange blend membranes composed of the following blend components:
A halomethylated polymer quaternized with a sterically hindered tertiary nitrogen compound (a polymer having ¨(CH2).-CH2-Hal groups, Hal = F, Cl, Br, I; x = 0-12, for example chloromethylated polystyrene or bromomethylated polyphenylene oxide;
Examples of sterically hindered tertiary nitrogen compounds are:
N
N r N r N N
' 1 ,2,4,7-tetramethy1-1 H- 1 ,2,4,5,6,7-hexamethyl- 1 ,2,5,7-tetramethy1-1 H-benzo[d]imidazole 1H-benzo[d]imidazole benzo[d]imidazole quinuclidin-3-ol quinuclidine OH N
NNA
1 ,2-dimethy1-1 H-1 ,4-diazabicyclo[2.2.2]octane benzo[d]imidazole N-1\1¨
1 ,2,4,5-tetramethyl- 1 ,3,4,5-tetramethyl- 1 ,3,5-trimethy1-1 H-pyrazole 1 H-imidazole 1H-pyrazole N N' 1 ,2-dimethy1-4,5-dipheny1-1 H-imidazole Examples for halomethylated polymers are:
Br HC.2 , Br/
CI Poly(epichlorohydrin) Poly(vinyl- halomethylated benzylchloride) Polyphenylenether Br AAA,0 = II
S = 0 bromomethylated Poly(ethersulfon) \B/
Br F F F H2C\ /CH2 Br Br bromomethylated partially fluorinated aromatic Polyether I
Br Br\cH2 0 O¨

F F F F H2C\
Br/CH2 Br bromomethylated partially fluorinated aromatic Polyether II
a matrix polymer, for example a basic polybenzimidazole; Examples of basic matrix polymers are:

H H
\ F6PBI /

N-.......,.--, N .
JVNAP _________ ( 1 I / =
N----\.% .\-----NI CF3 H H
\ S02PBI / 0 NI N 11 II =
I / S
I I
N----- \------N1 0 H H
\ /

JVW __________ (NI 101 1p / = 0 =

H H
\ / PBIO
1=1,....______/\_-. N .
1 / 0 .
14----\% \-----N1 H H
\ PBI Celazol / P4VP
N--____., .-N
sfvv-v- ______ ( 1 I , / I
1µ1"--\% \----1=1 N
H H H
1 para-PBI / AB-PBI /
1 \ 1 __ ( __ ) ¨ N
../VV V' ______ ( 1 -r1/4Ar sn ) ____ JVVV`
NI----\% \------N N
R R

I I
rv-tAr ________ 0 S

N¨) R= \/) ____________________________ (N N) \ /
\___ __ ______________________________ OH ________________________ OH __ N
------;----N ----"'-'-i, .%-"--- -.õ, I I
N N

- optionally a sulfonated aryl polymer as an ionic macromolecular crosslinker (ionic crosslinking with the basic functional groups of the matrix polymer and with the anion exchange groups of the quaternized halomethylated polymer.

Examples of sulfonated aryl polymers are:
sulfonated partially fluorinated aromatic polyether I (designation SFS001) F F F F

sulfonated partially fluorinated aromatic polyether II

_________________________ 0 0 sulfonated Poly(phenyleneethersulfone), statistic Copolymer (designation SAC098) ¨0 = 0 =
Ho3 03H Ho3 03H
sulfonated partially fluorinated aromatic polyethersulfone sulfonated partially fluorinated F F F F aromatic Poly(sulfone) ^^^-0 = ---s 0 cF3 Ho3 03H F F F F HO3S SO3H
sulfonated aromatic Poly(phenylphosphinoxide) I

HO3S 0 3 H it sulfonated aromatic Poly(phenylphosphinoxide) II

optionally a sulfonated polymer as a covalent macromolecular crosslinker whose sulfinate groups undergo covalent crosslinking via the sulfinate-S-alkylation with the halomethyl groups of the halomethylated polymer. As an example, the covalent crosslinking reaction between a sulfonated and a halomethylated polymer is shown:
Li CI 0 c/)--0 = 0 ____ avvv DMSO
-LiCI
ÃfS

The addition of a hydrophilic linear polyethylene glycol bearing functional groups on both chain ends which can undergo nucleophilic substitutions with the basic functional groups of the matrix polymer (examples: epoxide groups, halomethyl groups) and thereby covalently anchored in the blend membrane which leads to the following property enhancements of the anion exchange blend membranes:
To a significant increase in the anion conductivity towards the previously measured with best for anion exchange membranes conductivity values - to a significant improvement in the chemical stability in strongly alkaline solutions even at elevated temperatures (for example, 1 molar aqueous KOH
solution at 90 C.) - covalent crosslinking by the epoxide-terminated polyethylene glycols, which leads to a reduction in the swelling and thus to an improvement in the mechanical stability.
The crosslinking reaction of the polyethylene glycols with the basic groups of the matrix polymers is schematically illustrated below for the reaction of an epoxide group-terminated polyethylene glycol with the imidazole group moieties of a polybenzimidazole:

'NAP _____ N N)__( ____________ ) CF3e )_,õ
N N ¨ CF3 \¨
H I-I
\ n 0 H H
N N CF3 ¨
-v-v¨( )-----0 ( __ >---1."
N N i CF3 heat 1 >130 C
N3 ___________________________________________________ N\>_____<¨ CF ) CF ( )__,AA, rlf Vs _______ N
N 3 ¨

HOr____, z"-----4, kJ
----OH
H
N N/>---(___) ____ N N
Surprisingly, it has furthermore been found that the membrane properties such as conductivity and thermal and chemical stability, in particular stability in strongly alkaline solutions such as aqueous potassium hydroxide solution or sodium hydroxide solution can be further improved by a sulfinated polymer optionally added to the blend mixture. In particular, it has surprisingly been found that the sulfinate groups of the sulfinated polymer are capable of reaction with epoxy or halomethyl end groups of the polyethylene glycol, presumably under sulfinate S-alkylation of the sulfinate groups by the epoxide or halomethyl groups. The reaction of the sulfinate groups of the sulfinated polymer with the epoxide end groups of the polyethylene glycol are shown below:

Sil 0-4vvy _____________________________________ 0 __ O¨S

\O
Li 0 0¨S =

II =0-0 = Si, 0¨=^^^, DMSO

______________________ )-0 Sil S., OH

n 0 j0 r \0H
0 *

The anion-exchange blend membranes (AEBM) according to the invention can be obtained by means of three process routes:
1) The polymeric blend components (halomethylated polymer, matrix polymer (eg polybenzimidazole), polyethylene glycol with epoxide or halomethyl end groups, optionally sulfonated polymer and / or sulfinated polymer) are co-agitated in a dipolar aprotic solvent or in a mixture of different dipolar aprotic solvents (examples:

N, N-dimethylacetamide, N-methylpyrrolidinone, N-ethylpyrrolidinone, dimethylsulfoxide, sulfolane). Thereafter, the polymer solutions are doctored or cast on a support (glass plate, metal plate, plastic film, etc.), and the solvent is evaporated in a circulating air dryer or a vacuum oven at temperatures between room temperature and 150 C. Thereafter, the polymer film formed is removed from the backing and aftertreated as follows: 1) in a 10-50% solution of the tertiary amine or N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole in an alcohol (preferably ethanol or 2-propanol ) or in water or a water / alcohol mixture at temperatures from room temperature to the boiling point of the solvent for a period of 24-72 hours; 2) demineralized water at T = room temperature to T = 90 C
for a period of 24-72 hours; 3) 10% aqueous NaCl solution at T = room temperature to T =
90 C for a period of 24-72 hours; 4) DI water at T = room temperature to T =

for a period of 24-72 hours.
2) The polymeric blend components (halomethylated polymer, matrix polymer (eg polybenzimidazole), polyethylene glycol with epoxide or halomethyl end groups, optionally sulfonated polymer and / or sulfinated polymer) are co-mixed in a dipolar aprotic solvent or in a mixture of different dipolar aprotic solvents (examples: N, N-dimethylacetamide, N-methylpyrrolidinone, N-ethylpyrrolidinone, dimethylsulfoxide, sulfolane). Thereafter, the tertiary amine or the N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole is added either in bulk or dissolved in a dipolar aprotic solvent in a molar excess of 50-200%, based on the concentration of halomethyl groups, to the solution , Thereafter, the polymer solutions are doctored or cast on a support (glass plate, metal plate, plastic film, etc.), and the solvent is evaporated in a circulating air dryer or a vacuum oven at temperatures between room temperature and 150 C. Thereafter, the polymer film formed is removed from the support and aftertreated as follows: 1) optionally in a 10-50% solution of the tertiary amine or N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole in an alcohol (preferably ethanol or 2- Propanol) or in water or a water / alcohol mixture at temperatures from room temperature to the boiling point of the solvent for a period of 24-72 hours; 2) demineralized water at T = room temperature to T = 90 " C
for a period of 24-72 hours; 3) 10% aqueous NaCI solution at T = room temperature to T =

90 C for a period of 24-72 hours; 4) DI water at T = room temperature to T =

for a period of 24-72 hours.
3) All components of the polymer blend are separately dissolved in a dipolar aprotic solvent or a mixture of different dipolar aprotic solvents. Thereafter, the various solutions are combined in the desired mass ratio, and then continue with the resulting blend solution after homogenization as in the items 1) or 2).

Figure description Figure 1 shows the chloride conductivities of the membranes 2175 and 2176 in the temperature range between 30 and 90 0 C with a constant relative humidity of 90%.
Figure 2 shows the chloride conductivity of the membrane 2176 before and after 10, 20 and 30 days incorporation in 1M KOH in a temperature range of 30 to 90 C and a relative humidity of 90%.
Figure 3 shows the TGA curves of membranes 2175 and 2176 before and after 10 days treatment in 1M KOH at 900 C
Figure 4 shows the TGA curves of membrane 2176 before and after 10, 20 and 30 days treatment in 1M KOH at 90 C
Figure 5 shows the chloride conductivity of the membrane 2190A before and after 10 days storage in 1M KOH in the temperature range 30-90 C at a relative humidity of 90%
Figure 6 shows the TGA curves of membrane 2190A before and after 10 days storage in 1M KOH at Figure 7 shows the chloride conductivity of the membrane 2215 before and after 10 days storage in 1M KOH in the temperature range 30-90 C at a relative humidity of 90%
Figure 8 shows the TGA curves of membrane 2215 before and after 10 days storage in 1M KOH at 90 C
Figure 9 shows the chloride conductivity of the membrane 2179B before and after 10 days storage in 1M KOH in the temperature range 30-90 C at a relative humidity of 90%
Figure 10 shows the chloride conductivity of the membrane 2216 before and after 10 days storage in 1M KOH in the temperature range 30-90 C at a relative humidity of 90%
Figure 11 shows the chloride conductivity of the commercial anion exchange membrane Tokuyama A201 in the temperature range 30-80 C at a relative humidity of 90%

Application Examples Example 1: AEM blends of PVBCI, PB100, a sulfonated polyethersulfone (SAC098, see description) Tetramethylimidazole for quaternization of PVBC1 and an epoxide-terminated polyethylene glycol (membranes MJK2175 and MJK2176) Membrane production and aftertreatment:
12 g of a 10 % by weight solution of polyvinylbenzyl chloride (ALDRICH product no. 182532, structure see FIG. 2) in N,N-dimethylacetamide (DMAc) are mixed with 6 g of a 33.3% by weight solution of 1,2,4,5-tetramethy1-1H-imidazole (TCI Product No. T0971, see Figure 1 for structure), 6.7 g of a 10% by weight solution of PB100 (manufacturer FumaTech, structure see Figure 3) and 2.67 g of a 10% by weight solution of a sulfonated polyethersulfone (SAC098, IEC = 1.8 meq SO3H / g, see description) mixed in DMAc. In the case of membrane 2175, 0.25 g of epoxide-terminated polyethylene glycol (molecular mass 500 daltons, ALDRICH product no. 475696) are added to this mixture after homogenization, in the case of membrane 2176 0.25 g of epoxide-terminated polyethylene glycol ( Molecular mass 6000 daltons, ALDRICH product no. 731803). After homogenization, the polymer solutions are doctored on a glass plate. Thereafter, the solvent is evaporated in a convection oven at 130 *
C for a period of 2 hours. The polymer films are then removed under water and after-treated as follows:
- At 60 0 C for 24 hours in a 10% by weight solution of tetramethylimidazole in ethanol - At 90 0 C for 48 hours in a 10 wt% solution of NaCI in water - At 60 C for 48 hours in deionised water - Parts of the membranes are placed in an aqueous 1M KOH solution for a period of 10 days at a temperature of 90 0 C *
Membrane characterization:
Membrane 2175:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.92 / 2.96 - Conductivity before / after KOH treatment * (Cl- form, measured in 0.5N
NaCI at room temperature) [S / cm]: 29.3 / 72.7 - Water uptake at 25 0 C before / after KOH treatment * [%]: 367/324 Gel content after extraction in DMAc at 90 C before / after KOH treatment *
[%]: 97.6 / 100 Membrane 2176:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.79 / 2.84 - Conductivity before / after KOH treatment * (Cl- form, measured in 0.5N NaCI
at room temperature) [5 / cm]: 21.6 / 69.9 - Water uptake at 25 C before / after KOH treatment * [%]: 370/313 Gel content after extraction in DMAc at 90 C before / after KOH treatment *
[%]: 97.4 / 97 Comparison of Characterization Results of Membranes 2175 and 2176 Remarkable and surprising in the two membranes 2175 and 2176 of this application example was that the conductivity of the membranes after 10 days of KOH treatment was significantly higher than before the KOH treatment. Because of this surprising finding, the chloride conductivities were measured in another impedance measurement stand as a function of the temperature in a temperature range between 30 and 90 C at a constant relative humidity of 90%. The chloride conductivity vs. temperature curves of the two membranes 2175 and 2176 are shown in Figure 1. It shows, that:
1) both membranes have nearly equal conductivity curves;
2) even under these conditions, the conductivities measured after 10 days of KOH
incorporation were significantly higher than before, although the molecular masses of the epoxide-terminated polyethylene glycols (PEG) used in membrane production are very different (2175: PEG molecular mass 500 daltons; 2176: PEG molecular mass 6000 daltons) The gel content of the membranes of almost 100% surprisingly shows a complete formation of the network of these anion exchange blend membranes. Due to the excellent membrane stabilities, the storage time of membrane 2176 in 1M KOH at 90 C was extended by a further 20 days to a total of 30 days, and the membrane chloride conductivity was determined experimentally after a total of 20 days and after a total of 30 days in the temperature range from 30 to 90 C under a relative humidity of 90%. Figure 2 shows the chloride conductivities of the membrane 2176 before and after 10, 20 and 30 days incorporation in 1M KOH in the temperature range from 30 to 90 C. There was a surprising development: after 10 days, the conductivity of the membrane was greatly increased over before the KOH treatment, and then decreased to a slightly lower level after 20 days compared to before the KOH treatment. This value then no longer changed in the time interval between 20 and 30 days storage in KOH. Since the thermogravimetry (TGA) studies of the membranes can also give indications of degradation processes in the membranes, for the two membranes 2175 and 2176 TGA curves were recorded before and after the KOH
treatment. Figure 3 shows the TGA curves of membranes 2175 and 2176 before and after 10 days of treatment in 1M KOH at 90 C. From the TGA curves of both membranes no conclusions can be drawn on degradation processes in KOH solution, since the TGA curves of both membranes before and after 10 days of KOH treatment are almost congruent.

To determine if in 2176 membrane degradation occurs during the KOH long-term stability test of the membrane, TGA curves of the 2176 were recorded before and after 10, 20 and 30 days of incorporation in KOH. These TGA curves are shown in Figure 4. From Figure 4, it can be seen that the TGA curves of all 4 samples are nearly congruent up to a temperature of about 430 C, from which one can conclude that the 2176 still shows no sign of significant degradation even after 30 days of incorporation into KOH which confirms the results of the conductivity tests.
Example 2: AEM blend of PVBCI, PB100, a sulfonated polyethersulfone (SAC098, see description), tetramethylimidazole for quaternization of the PVBCI and an epoxide-terminated polyethylene glycol having a lower AEM content than in Application Example 1 but the same molar ratio between PB100 and PEG -Diepoxid 6000 (Membrane MJK2190A) Membrane production and aftertreatment:
12 g of a 10% by weight solution of polyvinylbenzyl chloride (ALDRICH product no. 182532, structure as described) in N, N-dimethylacetamide (DMAc) are mixed with 6 g of a 33.3% by weight solution of 1,2,4,5 -Tetramethy1-1H-imidazole (TCI product no. T0971, structure see description), 10.34 g of a 10 wt% solution of PB100 (manufacturer FumaTech, structure see description) and 2.67 g of a 10 wt% solution of a sulfonated polyethersulfone (SAC098, IEC =
1.8 meq 503H / g, structure see description) mixed in DMAc. After homogenization, 0.386 g of epoxide-terminated polyethylene glycol (molecular mass 6000 daltons, ALDRICH product no. 731803) are added to this mixture. After homogenization, the polymer solution is doctored onto a glass plate. Thereafter, the solvent is evaporated in a convection oven at 130 C for a period of 2 hours. The polymer film is then removed under water and after-treated as follows:
- At 60 C for 24 hours in a 10% strength by weight solution of tetramethylimidazole in ethanol - At 90 C for 48 hours in a 10 wt% solution of NaCl in water - At 60 C for 48 hours in deionised water Part of the membrane is placed in an aqueous 1M KOH solution for a period of 10 days at a temperature of 90 C *
Membrane characterization:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.1 / 2.7 - Conductivity before / after KOH treatment * (Cl- form, measured in 0.5N NaCl at room temperature) [S / cm]: 14.3 / 16.3 - Water absorption at 25 C before / after KOH treatment * [%]: 67 / 90.5 - Gel content after extraction in DMAc at 90 C before KOH treatment [%]:
95.9 As with the membranes 2175 and 2176, the chloride conductivity was also determined in this membrane as a function of the temperature between 30 and 900 C at a relative humidity of 90%. The conductivity curves are shown in Figure 5. Surprisingly, the conductivity of the 2190A membrane also increases during KOH treatment. In order to determine the thermal stability of the membrane and possible degradation processes in the membrane, TGA curves of the membrane were recorded before and after 10 days of KOH
treatment. The TGA curves are shown in Figure 6. Also in this membrane, the TGA curves before and after 10 days of KOH treatment almost congruent, at least up to a temperature of about 350 C, indicating that after 10 days of incorporation in 1M KOH at 90 C still no significant degradation of the membranes has taken place.
Example 3: AEM blend of PVBCI, F6PBI, a sulfonated partially fluorinated aromatic polyether (SF5001, see description), tetramethylimidazole for quaternization of the PVBCI and a double-sidedly epoxide-terminated polyethylene glycol having a molecular mass of 2000 daltons (membrane MJK2215) Membrane production and aftertreatment:
3 g of a 20% by weight solution of polyvinylbenzyl chloride (ALDRICH product no. 182532, structure see Figure 2) in dimethyl sulfoxide (DMSO) are mixed with 3 g of a 33.3% by weight solution of 1,2,4,5-tetramethyl 1H-imidazole (TCI Product No. T0971, see Figure 1 structure), 10.34 g of a 5% by weight solution of F6PBI (see structure in description) in DMSO and 1.11 g of a 10% by weight solution of a sulfonated partially fluorinated aromatic Polyether (SFS001) in S03Li form (IEC = 2.39 meq SO3H / g, structure see description) mixed in DMSO. After homogenization, 0.193 g of epoxide-terminated polyethylene glycol (molecular mass 2000 daltons, ALDRICH product no. 731811) are added to this mixture. After homogenization, the polymer solution is doctored onto a glass plate. Thereafter, the solvent is evaporated in a convection oven at 140 C for a period of 2 hours. The polymer film is then removed under water and after-treated as follows:
- At 60 C for 24 hours in a 10% strength by weight solution of tetramethylimidazole in ethanol - At 90 C for 48 hours in a 10 wt% solution of NaCI in water - At 60 C for 48 hours in deionised water Part of the membrane is placed in an aqueous 1M KOH solution for a period of 10 days at a temperature of 90 C *
Membrane characterization:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.37 / 2.7 Conductivity before! after KOH treatment * (Cl-form, measured in 0.5N NaCI at room temperature) [S / cm]: 37.2 / 29.2 - Water uptake at 25 C before / after KOH treatment * [%]: 56.7 / 68 - Gel content after extraction in DMAc at 90 C before KOH treatment [%]:
92.7 As with the membranes 2175 and 2176 as well as 2190A, the chloride conductivity was also determined in this membrane as a function of the temperature between 30 and 90 C at a relative humidity of 90%. The conductivity curves are shown in Figure 7.
Again, as in the previous examples, the chloride conductivity after 10d storage in 1M KOH at 90 C is higher than before. In order to determine the thermal stability of the membrane and possible degradation processes in the membrane, TGA curves of the membrane were recorded before and after 10 days of KOH treatment. The TGA curves are shown in Figure 8. Also in this membrane, the TGA curves before and after 10 days of KOH treatment almost congruent, at least up to a temperature of about 350 C, indicating that after 10 days of incorporation in 1M KOH at 90 C still no significant degradation of the membranes has taken place.
Comparative Example 1: AEM blend of PVBCI, PB100, a sulfonated polyethersulfone (SAC098, see description), tetramethylimidazole for quaternization of the PVBCI with the same calculated IEC as the membranes MJK2175 and MJK2176, but without PEG
diglycidyl ether (membrane 2179B) Membrane production and aftertreatment:
6 g of a 10% by weight solution of polyvinylbenzyl chloride (ALDRICH product no. 182532, structure see description) in DM50 are mixed with 2.2 g of a 33.3% by weight solution of 1,2,4,5-tetramethy1-1H- lmidazole (TCI product no. T0971, see structure for description) in DMAc, 4.6 g of a 10% strength solution of PB100 (manufacturer FumaTech, structure see description) in DMAc and 1.335 g of a 10% by weight solution of a sulfonated polyethersulfone ( SAC098, IEC = 1.8 meq SO3H / g, structure see description) mixed in DMAc. After homogenization, the polymer solutions are doctored on a glass plate.
Thereafter, the solvent is evaporated in a convection oven at 140 C for a period of 2 hours.
The polymer films are then removed under water and after-treated as follows:
- At 60 C for 24 hours in a 10% strength by weight solution of tetramethylimidazole in ethanol - At 90 C for 48 hours in a 10 wt% solution of NaCI in water - At 60 C for 48 hours in deionised water - Parts of the membranes are placed in an aqueous 1M KOH solution for a period of 10 days at a temperature of 90 C *
Membrane characterization:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.5 / 2.64 Conductivity before / after KOH treatment * (Cl-form, measured in 0.5N NaCI at room temperature) [S / cm]: 10.7 / 15.9 - Water uptake at 25 C before / after KOH treatment * [%]: 63/87 Gel content after extraction in DMAc at 90 C before KOH treatment * [%]:
94.2 If these data are compared with those of membranes 2175 and 2176, the following results:
- The Cl - conductivity is much lower than in the two membranes of the invention. This shows what a positive influence the addition of a hydrophilic PEG phase has to the membrane - Water uptake is significantly lower than at 2175 and 2176. This can be explained by the lower hydrophilicity of the control membrane.
Since the Cl conductivity of the 21798 was higher in conductivity measurement at room temperature and in 0.5N NaCI as at 2175 and 2176 after the KOH treatment, the impedance of the 21798 was again measured in dependence of the temperature at a relative humidity of 90%. The conductivity curve of the 2179B under these conditions is shown in Figure 9.
Here, it is found that, as in the impedance measurement at room temperature in 0.5M NaCI, the chloride conductivity is much lower than that of the 2175 and 2176 containing a PEG
phase and that the impedance after KOH treatment is significantly lower than before. Since at 2175 and 2176 the chloride conductivity was higher after 10d KOH treatment than before, on the one hand shows the conductivity-increasing effect and on the other hand, the stabilizing effect of the presence of a PEG microphase in the blend AEMs.
Comparative Example 2: AEM blend of PVBCI, F6PBI, a sulfonated partially fluorinated polyether (SFS001, see description), tetramethylimidazole for quaternization of PVBCI
with the same calculated IEC as the membrane MJK2215, but without PEG
diglycidyl ether (membrane 2216) Membrane production and aftertreatment:
3 g of a 20% by weight solution of polyvinylbenzyl chloride (ALDRICH product no. 182532, structure as described) in DMSO are mixed with 3 g of a 33.3% by weight solution of 1,2,4,5-tetramethy1-1H-imidazole (ICI Product No. T0971, structure see description) in DMSO, 14.2 g of a 5 wt% solution of F6PBI (structure see description) in DMSO and 1.1 g of a 10 wt%
solution of the sulfonated polyether SF5001 (IEC = 2.39 meq SO3H / g, structure see description) mixed in DMSO. After homogenization, the polymer solutions are doctored on a glass plate. Thereafter, the solvent is evaporated in a convection oven at 140 C for a period of 2 hours. The polymer film is then removed under water and after-treated as follows:
- At 60 C for 24 hours in a 10% strength by weight solution of tetramethylimidazole in ethanol - At 90 C for 48 hours in a 10 wt% solution of NaCI in water - At 60 C for 48 hours in deionised water - Parts of the membranes are placed in an aqueous 1M KOH solution for a period of 10 days at a temperature of 90 C.
Membrane characterization:
- ion exchange capacity before / after KOH treatment * [meq OH- / g membrane]:
2.48 / 2.7 - Conductivity before / after KOH treatment (Cl- form, measured in 0.5N NaCI
at room temperature) [S / cm]: 7.4 / 8.2 - Water absorption at 25 C before / after KOH treatment [%]: 44/33 - Gel content after extraction in DMAc at 90 C before KOH treatment * [%]:
95.7 If these data are compared with those of the membrane 2215, the following results:
- The Cl - conductivity at room temperature in 0.5N NaCI is significantly lower than in the inventive membrane 2215. This shows the positive influence of the addition of a hydrophilic PEG phase has to the membrane.
- The water absorption is significantly lower than at 2215. This can be explained by the lower hydrophilicity of the control membrane.
Since the Cl conductivity of the 2216 was higher in the conductivity measurement at room temperature and in 0.5N NaCI as in 2215 after the KOH treatment, the impedance of the 2215 was again measured as a function of the temperature at a relative humidity of 90%.
measured. The conductivity curve of the 2215 under these conditions is shown in Figure 10.
Here it can be seen that, as in the impedance measurement at room temperature in 0.5M
NaCI, the chloride conductivity is much lower than in the 2215 containing a PEG phase, and that the impedance after the KOH treatment is significantly lower than before.
Comparative Example 2 shows, as in Comparative Example 1, on the one hand, the conductivity-increasing effect and, on the other hand, the stabilizing effect of the presence of a PEG
microphase in the blend AEMs.

Comparative Example 3: Commercial anion exchange membrane A201 (development code A006) of the manufacturer Tokuyama The structure of this membrane is company secret. The anion exchange group of this membrane is the trimethylammonium group. But it is obviously a cross-linked membrane because the extraction of the membrane gave a gel content of 95%.
Membrane characterization:
- Ion exchange capacity [meq OH / g membrane]: 1.7 - Conductivity (Cl- form, measured in 1 N NaCI at room temperature) [S / cm]:

- Water absorption at 30 C [%]: 19 - Gel content after extraction in DMAc at 90 C before KOH treatment *
[%]: 95 - Conductivity (Cl- form, measured at 90 C and 90% relative humidity, after 10d incorporation in 1M KOH at 900 C): 21% of the original conductivity This commercial membrane is thus much less stable in 1M KOH at 90 C compared to the membranes of the invention. In addition, the chloride conductivity of this membrane is substantially lower than most of the membranes of this invention listed as examples in this chapter. The chloride conductivity of the A201 in the temperature range of 30 to 80 C at 90% relative humidity is shown in Figure 11.
Comparative Example 4: Commercial anion exchange membrane FAB from the manufacturer Fuma-Tech The structure of this membrane is company secret. But it is obviously a cross-linked membrane, as the extraction of the membrane gave a gel content of 93.3%.
Membrane characterization:
- Ion exchange capacity before / after 10d in 1M KOH at 90 C [meq OH- / g membrane]:
0.88 / 0.89 - Conductivity before / after 10d in 1M KOH at 90 C (Cl- form, measured in 1 N NaCI at room temperature) [S / cm]: 4 / 3.2 - Water absorption at room temperature / at 90 C C [%]: 12.1 / 13.2 Gel content after extraction in DMAc at 90 C before / after KOH treatment *
[%]: 93.3 / 97 The chloride conductivity of this membrane is substantially lower than that of most of the , membranes of this invention listed as examples, which is also (among others) because this membrane is fabric-reinforced.

Claims (14)

Patent Claims
1 Anion-exchange blend membrane, characterized in that it consists of the following blend components:
- a halomethylated polymer with functional groups ¨(CH2)x-CH2Hal (Hal = F, CI, Br, I; x = 0-12) reacted with a tertiary amine or an alkylated imidazole or an alkylated pyrazole or an alkylated benzimidazole to quaternize cationic functional groups - a basic or neutral non-fluorinated or partially fluorinated inert matrix polymer - a polyethylene glycol with epoxy or halomethyl end groups at one or both ends of the chain - optionally a polymer having acidic functional groups SO3M, P03M2 or COOM (M
=
any cation) - optionally with a polymer containing sulfinate groups SO2M (M = any Cation).
2 Anion-exchange blend membrane according to claim 1, characterized in that are used as the halomethylated polymers polymers with CH2Br or with CH2CI groups.
3 Anion-exchange blend membrane according to claim 1, characterized in that the following classes of polymers are preferred as halomethylated polymers:
- Polyvinylbenzyl chloride (chloromethylated polystyrene) and its copolymers with any other polymers - Chloromethylated poly (a-methylstyrene) and its copolymers with any other polyrners Halomethylated aryl main chain polymers, such as halomethylated Polyketones, halomethylated polyether ketones, halomethylated polysulfones, halomethylated polyethersulfones, halomethylated polyethers, halomethylated Polyphenylphosphine oxides or halomethylated polyphenylphosphine oxide ethers with the following building groups (polymer backbone):

Aromatic building blocks (shown without CH2Hal- groups, which are bound to these building blocks):
Ro = Roa =
Y Y
R2=H or =C,1-12n_1, CnHal211_1, preferentially CF3 _ R2 _ Ri = ¨( ) ________ R2 ( )¨ Ria -- ) ( Y=cation-exchange group (see below) Y Y

¨N
R3 = 4. R3a = R4 - __ ( ) F F F F
Ria - ., R5 = R6 = Z
Y
F F F F
Z= bridging group (see below) F F F F F F F Y
R7 = Rg = Rga =
F F F F F F F

Rg = Rga = R1o=

Y=cation-exchange group (see below) ¨N ¨N
Rioa = Rii- Rila-Cation-exchange groups Y:

// // II II
¨C ¨S\ ¨S-0Me ¨P¨OMe \ 11 1 OMe OMe 0 OMe Me = beliebiges Kation (H+, Li+, Ne, r, Rb+, ce, etc.) Bridging groups Z:

II II II II
¨0¨ ¨S¨ ¨S¨ ¨S¨ ¨P¨ ¨C-0 .
4 Anion-exchange blend membrane according to claim 1, characterized in that as tertiary amines or alkalized imidazoles or alkylated pyrazoles or alkylated benzimidazoles, the following sterically hindered compounds are preferred:

N N' N" .. 1 ' N¨

N ' N¨

IP * .
1,2,4,7-tetramethyl-1 H- 1,2,4,5,6,7-hexamethyl- 1,2,5,7-tetramethyl-1H-benzo[c]imidazole 1H-benzo[d]imidazole benzo[d]imidazole quinuclidin-3-ol quinuclidine OH N N' N N N *
\ \ __ / \ 1,2-dimethyl-1 H-benzo[djimidazole 1,4-diazabicyclo[2.2.2]octane )¨ N¨ ---NI
h-1,2,4,5-tetramethyl- 1,3,4,5-tetramethyl- 1,3,5-trimethyl-1H-pyrazole 1H-imidazole 1H-pyrazole /( N / N--db 1,2-dimethyl-4,5-diphenyl-1H-imidazole Anion exchange blend membrane according to claim 1, characterized in that basic polymers such as polyimides, polyetherimides, polybenzimidazoles, polybenzoxazoles, polybenzotriazoles or partially fluorinated polymers such as polyvinyl fluoride or polyvinylidene fluoride or partially fluorinated polystyrenes are preferred as the matrix polymer.
6 Anion exchange blend membrane according to claim 1, characterized in that the polyethylene glycols (PEG), which are used as a hydrophilic membrane component, carry as end groups at both chain ends epoxide groups or halomethyl CH2Hal (Hal = F, CI, Br, l) and have molecular masses of 200 daltons (corresponds to about 4 -0- units) up to 12,000 daltons (equivalent to about 200 -CH2-CH2-0- units), with PEGs having molecular masses between 500 and 6,000 daltons being preferred:
PEG with Epoxide end groups (n=4 to 200) PEG with Halomethyl end groups (n=4 to 200) Hal=F, CI, Br, I) a I
Hal 0
7 Anion exchange blend membrane according to claim 1, characterized in that aryl main chain polymers which comprise the families of aromatic polyethers, polyketones, polyether ketones, polysulfones, polyethersulfones, polyphenylphosphine oxides, polyphenylphosphine oxide ethers and thioethers, polythioethersulfones having the building groups of claim 3 are preferred as polymers having acidic functional groups
8 Anion-exchange blend membrane according to claims 1 and 7, characterized in that the sulfonate group SO3M is preferred as the acidic functional group (M = any cation)
9 Anion exchange membrane according to claims 1 and 7, characterized in that the polymer carrying the sulfinate functional groups SO2M has one of the aryl main chains (polymer backbone) listed in claim 7 (M = any cation).
Process for the preparation of the anion exchange blend membranes according to the invention according to Claims 1 to 9, characterized in that it consists of the following process steps:
The polymeric blend components (halomethylated polymer, matrix polymer (eg, polybenzimidazole), epoxide or halomethyl terminated polyethylene glycol, optionally sulfonated polymer, and / or sulfinated polymer) are used together in a dipolar aprotic solvent or in a mixture of various dipolar aprotic solvents (Examples:

N, N-dimethylacetamide, N-methylpyrrolidinone, N-ethylpyrrolidinone, dimethylsulfoxide sulfolane). Thereafter, the polymer solutions are doctored or cast on a support (glass plate, metal plate, plastic film, etc.), and the solvent is evaporated in a circulating air dryer or a vacuum oven at temperatures between room temperature and 150 C. Thereafter, the polymer film formed is removed from the backing and aftertreated as follows: 1) in a 10-50% solution of the tertiary amine or N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole in an alcohol (preferably ethanol or 2-propanol ) or in water or a water / alcohol mixture at temperatures from room temperature to the boiling point of the solvent for a period of 24-72 hours; 2) demineralized water at T = room temperature to T = 90 C
for a period of 24-72 hours; 3) 10% aqueous NaCI solution at T = room temperature to T =
90 C for a period of 24-72 hours; 4) DI water at T = room temperature to T =

for a period of 24-72 hours.
11 Process for the preparation of the inventive anion-exchange blend membranes according to claims 1 to 9, characterized in that it consists of the following process steps:
The polymeric blend components (halomethylated polymer, matrix polymer (eg, polybenzimidazole), epoxide or halomethyl terminated polyethylene glycol, optionally sulfonated polymer, and / or sulfinated polymer) are used together in a dipolar aprotic solvent or in a mixture of various dipolar aprotic solvents (Examples:
N, N-dimethylacetamide, N-methylpyrrolidinone, N-ethylpyrrolidinone, dimethylsulfoxide sulfolane). Thereafter, the tertiary amine or the N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole is added either in bulk or dissolved in a dipolar aprotic solvent in a molar excess of 50-200%, based on the concentration of halomethyl groups, to the solution , Thereafter, the polymer solutions are doctored or cast on a support (glass plate, metal plate, plastic film, etc.), and the solvent is evaporated in a circulating air dryer or a vacuum oven at temperatures between room temperature and 150 C. Thereafter, the polymer film formed is removed from the support and aftertreated as follows: 1) optionally in a 10-50% solution of the tertiary amine or N-monoalkylated (benz) imidazole or N-monoalkylated pyrazole in an alcohol (preferably ethanol or 2- Propanol) or in water or a water /
alcohol mixture at temperatures from room temperature to the boiling point of the solvent for a period of 24-72 hours; 2) demineralized water at T = room temperature to T =
90 C for a period of 24-72 hours; 3) 10% aqueous NaCI solution at T = room temperature to T = 90 C for a period of 24-72 hours; 4) DI water at T = room temperature to T = 90 C for a period of 24-72 hours.
12 A process for the preparation of the inventive anion-exchange blend membranes according to claims 1 to 9, characterized in that it consists of the following process steps: All components of the polymer blend are dissolved separately in a dipolar aprotic solvent or a mixture of different dipolar aprotic solvents.
Thereafter, the various solutions are combined in the desired mass ratio, and then with the resulting blend solution after homogenization as in the claims 11 or 12 further.
13 Use of the membranes according to claims 1 to 12 in membrane processes, especially in low temperature PEM fuel cells, PEM medium temperature fuel cells, PEM
electrolysis, S02 depolarized electrolysis, redox flow batteries, other flow batteries, electrodialysis, diffusion dialysis, nanofiltration, ultrafiltration , Reverse osmosis and pressure-retarded osmosis.
14 Use of the membranes according to claims 1 to 12 as a component of sensors, electrodes, secondary batteries, fuel cells, alkaline fuel cells or membrane electrode units.
CA3066028A 2019-12-23 2019-12-23 Crosslinked highly stable anion-exchange blend membranes with polyethyleneglycols as the hydrophilic membrane phase Abandoned CA3066028A1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114540877A (en) * 2022-02-25 2022-05-27 西湖大学 Method for treating anion exchange membrane by solvothermal method and application thereof
CN115746560A (en) * 2022-10-20 2023-03-07 北京和瑞储能科技有限公司 Amphiphilic alcohol self-assembly induced sulfonated polybenzimidazole ion exchange composite membrane and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114540877A (en) * 2022-02-25 2022-05-27 西湖大学 Method for treating anion exchange membrane by solvothermal method and application thereof
CN114540877B (en) * 2022-02-25 2023-10-31 西湖大学 Method for treating anion exchange membrane by solvothermal method and application thereof
CN115746560A (en) * 2022-10-20 2023-03-07 北京和瑞储能科技有限公司 Amphiphilic alcohol self-assembly induced sulfonated polybenzimidazole ion exchange composite membrane and preparation method thereof
CN115746560B (en) * 2022-10-20 2024-02-09 北京和瑞储能科技有限公司 Amphiphilic alcohol self-assembly induced sulfonated polybenzimidazole ion exchange composite membrane and preparation method thereof

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