US20120134905A1

US20120134905A1 - Method of use of an ionic liquid and device for sorption of a gas

Info

Publication number: US20120134905A1
Application number: US13/380,008
Authority: US
Inventors: Roland Kalb
Original assignee: VTU Holding GmbH
Current assignee: Proionic GmbH
Priority date: 2009-06-25
Filing date: 2010-06-22
Publication date: 2012-05-31
Also published as: JP2016013551A; US9011576B2; KR20120047232A; BRPI1014757A2; CN102481513B; CN105289208A; US20110247494A1; CN102481513A; EP2445613A1; WO2010149674A1; JP2012530598A

Abstract

A method of use of an ionic liquid for sorption of a gas having an electric multipole moment is provided, wherein the ionic liquid comprises an anion and a non-aromatic cation. In particular, the electric multipole moment may be an electric dipole moment and/or an electric quadrupole moment. The sorption may be an adsorption or an absorption. The ionic liquid may be a pure ionic liquid, i.e. a liquid substantially only containing anions and cations, while not containing other components, e.g. water. Alternatively a solution containing the ionic liquid and a solvent or further compound, e.g. water, may be used.

Description

FIELD OF THE INVENTION

The invention relates to a method of use of an ionic liquid, in particular for sorption of a gas or vapor having an electric multipole moment.
Further, the invention relates to a device for sorption of a gas or vapor.

BACKGROUND OF THE INVENTION

Carbon dioxide (CO₂) is an undesired diluent that is present in many gas sources. In order to improve the quality of the gases the CO₂should be removed to acceptable specifications. In gas processing industry, various technologies have been employed for CO₂removal including chemical solvents, physical solvents, and membranes. By far, chemical solvents that reversibly react with CO₂are most commonly used for CO₂removal.
Furthermore, processes for removal of CO₂from gaseous streams are known, which comprise the contacting a CO₂containing gaseous stream with an absorbent comprising from 1 to 20 wt % water and an ionic liquid comprising pyridines or imidazole cations and an anion, wherein said contacting occurs at absorption conditions, to absorb at least a portion of the CO₂from the CO₂containing gaseous stream and forming a CO₂-absorbent complex. Afterwards the gaseous product having a reduced CO₂content is recovered.
However, the known processes of removal CO₂may be costly.

OBJECT AND SUMMARY OF THE INVENTION

It may be an objective of the invention to provide a method of removal of a gaseous or vaporous component and a device for removal of a gaseous or vaporous component which may be save to use or less expensive than known methods.
This object may be solved by a method of use of an ionic liquid, in particular for sorption of a gas or vapor having an electric multipole moment and a device for sorption of a gas or vapor according to the independent claims. Further exemplary embodiments are described in the dependent claims.
According to an exemplary aspect of the invention a method of use of an ionic liquid for sorption of a gas having an electric multipole moment is provided, wherein the ionic liquid comprises an anion and a non-aromatic cation. It should be noted that according to this application the terms “gas” and “gaseous” and “vapor” and “vaporous”, respectively may be interchangeably used, i.e. no distinction is made between these two terms.
In particular, the electric multipole moment may be an electric dipole moment and/or an electric quadrupole moment. The sorption may be an adsorption or an absorption. The ionic liquid may be a pure ionic liquid, i.e. a liquid substantially only containing anions and cations, while not containing other components, e.g. water. Alternatively a solution containing the ionic liquid and a solvent or further compound, e.g. water, may be used. For example, the content of other components than the ionic liquid may be 35% or less by mass, in particular less than 30% by mass, less than 20% by mass, less than 10% by mass, or even less than 5% by mass, wherein for all the above ranges the lower limit may be about 10 ppm. However, in case of water as the other component the ranges may be between about 10 ppm and 50% by mass, in particular between about 10 ppm and 35% by mass, between about 10 ppm and 20% by mass, between about 10 ppm and 10% by mass, or even between about 10 ppm and 5% by mass. In this context it should be noted that according to specific embodiments the sorption may be performed by the ionic liquid itself, e.g. may particularly be a physical sorption. In general, the ionic liquid may also perform a chemical sorption, a physical sorption or a combined chemical-physical sorption. This process has to be distinguished from a process in which the ionic liquid only forms a solvent for a compound or component, e.g. a polymer, which then acts as the sorbent for the gas having an electric multipole moment. That is, according to specific embodiments of the invention the ionic liquid may form the sorbent which sorbs the gas having an electric multipole moment. Consequently a method according to an exemplary embodiment may comprise the step of sorbing a gas having an electric multipole moment by an ionic liquid, wherein the ionic liquid may be a pure or substantially pure ionic liquid or may include some additives having only few, e.g. less than 35% by mass, further components. In the most generic form the ionic liquids may be represented by [Q⁺]_n[Z^n-], wherein Q represents a non-aromatic cation and which may be produced by a process as described for example in WO 2005/021484 which is hereby herein incorporated by reference.
According to an exemplary aspect of the invention a device for sorption of a gas having an electric multipole moment is provided, wherein the device comprises a reservoir of an ionic liquid comprising an anion and a non-aromatic cation.
In particular, the device may comprise an inlet, a container including the ionic liquid, and optionally an outlet. The device may be used to sorb gas having an electric multipole moment, e.g. CO₂, from a medium which is selected out of the group consisting of recovery gas, synthesis gas, water gas, natural gas, inhaled air, and exhaled air. In particular, the device may be a heat pump. The heat pump may comprise a circuit including CO₂and the ionic liquid which comprises an anion and a non-aromatic cation as working media. In particular, the usage of a pair of working media containing CO₂and an ionic liquid in a heat pump may be advantageous since CO₂is not toxic is of less concern with respect to environmental effect compared to other vaporizable working substances.
According to an exemplary aspect of the invention a method of use of an ionic liquid for sorption of a gas having an electric multipole moment is provided, wherein the ionic liquid comprises a carbanion and a cation.
The use of non-aromatic cations of the ionic liquid may provide for an ionic liquid which may be cheaper and more secure than the use of aromatic cations. Such ionic liquids may be a suitable medium to sorb specific gases, e.g. CO₂, or vapor out of a mixture of gases and may also be suitable to release these specific gases or vapor again. The specific gases and the ionic liquid may form a complex, i.e. the specific gases may be complex bound. According to some exemplary embodiments it may even be possible to remove the complex bound in the form of a solid compound. The uses of such ionic liquids for sorption of gases may be advantageous since ionic liquids may be used showing no or at least substantially no vapor pressure, e.g. a non measureable vapor pressure or even a vapor pressure in the same magnitude of order of steel. Thus, the gases or mixture of gases may not be contaminated by vapor of the ionic liquid. Furthermore, the use of non-aromatic ionic liquids may increase the performance of the sorption process compared to the case in which aromatic ionic liquids are used. For example, the removal of CO₂by using non-aromatic ionic liquids may exhibit an improved performance even in cases where the vapor pressure of CO₂is low.
However, alternatively it may also be possible to use an ionic liquid having aromatic cation in case the ionic liquid comprises a carbanion. That is, when using an ionic liquid comprising a carbanion the cation may be an aromatic or a non-aromatic anion.
Next, further aspects of exemplary embodiments of the method of use of an ionic liquid for sorption of a gas are described. However, these embodiments also apply for the device for sorption of a gas.
According to an exemplary embodiment of the method of use of an ionic liquid the non-aromatic cation is an aliphatic cation. The term “aliphatic cation” may also include cations having aliphatic side chains.
Aliphatic cations may be suitable non-aromatic cations for an ionic liquid which are less expensive and/or less toxic than typical aromatic cations.
According to an exemplary embodiment of the method of use of an ionic liquid the ionic liquid satisfy the generic formula [Q⁺][A⁻],
wherein the anion can be described by one of the following structures:
In particular, the anion may be describable by the resonant or mesomeric states:
wherein X and Y may indicate, independently from each other, groups which may attract electrons due to the inductive effect or the mesomeric effect and/or which may delocalize and/or stabilize (localize) electrons. Examples for such groups may be:

- —CN, —NO₂, —NO₃, —CO—R^k, —COOR^k, —C═N—R^k, —CO—NR^kR^m, —NR^kR^m, —OH, —OR^k, —SH, —SR^k, —SO—R^k, —SO₂—R^k, —SO₂—OR^k, —PO—OR^kOR^m(phosphonate), —I, —Cl, —Br, —F, —CCl₃, —CCl₂R^k, —CClR^kR^m, —CF₃, —CF₂R^k, —CFR^kR^m, —SO₂CF₃, —COOCF₃, —C₆H₅, —CR^k═CR ^mRⁿ, —C≡CR^m, CR^k═CR^m—CN, —CR^k═CR^m—NO₂, —CR^k═CR^m—CO—R^k, —CR^k═CR^m—COOR^k, —CR^k═CR^m—C═N—Rⁿ, —CR^k═CR^m—CO—NRⁿR^o, —CR^k═CR^m—NRⁿR^o, —CR^k═CR^m—ORⁿ, —CR^k═CR^m—SRⁿ, CR^k═CR^m—SO—Rⁿ, —CR^k═CR^m—SO₂—Rⁿ, —CR^k═CR^m—SO₂—Rⁿ, —CR^k═CR^m—SO₂—ORⁿ, —CR^k═CR^m—CF₃, —CR^k═CR^m—SO₂CF₃,
  wherein R^k, R^m, Rⁿ, R^omay, independently from each other, denote hydrogen, C₁- to C₃₀-alkyl and their aryl-, heteroaryl-, cycloalkyl-, halogen-, hydroxy-, amino-, carboxy-, formyl-, —O—, —CO—, —CO—O— or —CO—N< substituted components, like methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methyl-1-propyl (isobutyl), 2-methyl-2-propyl (tert.-butyl), 1-pentyl, 2-pentyl, 3-pentyl, 2-methyl-1-butyl, 3-methyl-1-butyl, 2-methyl-2-butyl, 3-methyl-2-butyl, 2,2-dimethyl-1-propyl, 1-hexyl, 2-hexyl, 3-hexyl, 2-methyl-1-pentyl, 3-methyl-1-pentyl, 4-methyl-1-pentyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 2-methyl-3-pentyl, 3-methyl-3-pentyl, 2,2-dimethyl-1-butyl, 2,3-dimethyl-1-butyl, 3,3-dimethyl-1-butyl, 2-ethyl-1-butyl, 2,3-dimethyl-2-butyl, 3,3-dimethyl-2-butyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, icosyl, henicosyl, docosyl, tricosyl, tetracosyl, pentacosyl, hexacosyl, heptacosyl, octacosyl, nonacosyl, triacontyl, phenylmethyl (benzyl), diphenylmethyl, triphenylmethyl, 2-phenylethyl, 3-phenylpropyl, cyclopentylmethyl, 2-cyclopentylethyl, 3-cyclopentylpropyl, cyclohexylmethyl, 2-cyclohexylethyl, 3-cyclohexylpropyl, methoxy, ethoxy, formyl, acetyl or C_nF_{2(n−a)+(1−b)}H_2a+bwherein n≦30, 0≦a≦n and b=0 or 1 (e.g. CF₃, C₂F₅, CH₂CH₂—C_(n−2)F_2(n−2)+1, C₆F₁₃, C₈F₁₇, C₁₀F₂₁, C₁₂F₂₅);

C₃- to C₁₂-cycloalkyl and their aryl-, heteroaryl-, cycloalkyl-, halogen-, hydroxy-, amino-, carboxy-, formyl-, —O—, —CO— or —CO—O-substituted components, e.g. cyclopentyl, 2-methyl-1-cyclopentyl, 3-methyl-1-cyclopentyl, cyclohexyl, 2-methyl-1-cyclohexyl, 3-methyl-1-cyclohexyl, 4-methyl-1-cyclohexyl or C_nF_{2(n−a)−(1−b)}H_2a−bwherein n≦0, 0≦a≦n and b=0 or 1;
C₂- to C₃₀-alkenyl and their aryl-, heteroaryl-, cycloalkyl-, halogen-, hydroxy-, amino-, carboxy-, formyl-, —O—, —CO— or —CO—O-substituted components, e.g. 2-propenyl, 3-butenyl, cis-2-butenyl, trans-2-butenyl or C_nF_{2(n−a)−(1−b)}H_2a−bwherein n≦30, 0≦a≦n and b=0 or 1;
C₃- to C₁₂-cycloalkenyl and their aryl-, heteroaryl-, cycloalkyl-, halogen-, hydroxy-, amino-, carboxy-, formyl-, —O—, —CO— or —CO—O-substituted components, e.g. 3-cyclopentenyl, 2-cyclohexenyl, 3-cyclohexenyl, 2,5-cyclohexadienyl or C_nF_{2(n−a)−3(1=b)}H_2a−3bwherein n≦0, 0≦a≦n and b=0 or 1; and
aryl or heteroaryl having 2 to 30 carbon atoms and their alkyl-, aryl-, heteroaryl-, cycloalkyl-, halogen-, hydroxy-, amino-, carboxy-, formyl-, —O—, —CO— or —CO—O-substituted components, e.g. phenyl, 2-methyl-phenyl (2-tolyl), 3-methyl-phenyl (3-tolyl), 4-methyl-phenyl, 2-ethyl-phenyl, 3-ethyl-phenyl, 4-ethyl-phenyl, 2,3-dimethyl-phenyl, 2,4-dimethyl-phenyl, 2,5-dimethyl-phenyl, 2,6-dimethyl-phenyl, 3,4-dimethyl-phenyl, 3,5-dimethyl-phenyl, 4-phenyl-phenyl, 1-naphthyl, 2-naphthyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 2-pyridinyl, 3-pyridinyl, 4-Pyridinyl or C₆F_(5−a)H_awherein 0≦a≦5,
wherein pairs of the R^k, R^m, Rⁿ, R^omay be bonded directly to each other or via C₁-C₄, which may be substituted if necessary, so that a saturated, unsaturated, or conjugated unsaturated ring may be formed.
According to an exemplary embodiment of the method of use of an ionic liquid the ionic liquid satisfy the generic formula [Q⁺]_a[A^a-], wherein [A^a-] with the charge a- is selected out of the group consisting of:
dialkyl ketones, dialkyl-1,3-diketones, alkyl-β-keto esters, terminal alkines, linear or cyclic 1,3-thioethers, dialkyl phosphonates, dialkyl malonic acid esters, β-cyano carbonic acids and their respective alkylesters, β-alkoxy carbonic acids and their respective alkylesters, β-cyano nitriles, cyclopentadiene (substituted if necessary), trialkylimines, dialkylimines, diaryl ketones, alkyl-aryl-ketones, diary)-1,3-diketones, alkyl-aryl-1,3-diketones, β-aryloxy carbonic acids and their respective alkylesters, β-aryloxy carbonic acids and their respective arylesters, aryl-β-ketoesters, diarylphosphonates, alkyl-aryl-phosphonates, diaryl malonic acid esters, alkyl-aryl-malonic acid esters, β-cyano carbonic acids arylesters and arylimines.
According to an exemplary embodiment of the method of use of an ionic liquid the ionic liquid satisfy the generic formula [Q⁺]_a[A^{a-],wherein [A} ^a-] is a carbanion formed by deprotonating a chemical compound out of the group consisting of:
acetoacetic ester, malonic mononitrile, malonic acid dimethylester, malonic acid diethylester, acetylacetone, malonic acid dinitrile, acetone, diethylketone, methlethylketone, dibutylketone, 1,3-dithian, acetaldehyde, benzaldehyde, crotonaldehyde and butyraldehyde.
According to an exemplary embodiment of the method of use of an ionic liquid the ionic liquid satisfy the generic formula [Q⁺]_a[A^a-], wherein [A^a-] is a carbanion and wherein [C]⁺ is one out of the group consisting of quaternary ammonium cation [R^1′R¹R²R³N]⁺, phosphonium [R^1′R¹R²R³P]⁺, sulfonium [R^1′R¹R²S]⁺ and a hetero aromatic cation. In particular, the carbanion may be formed by deprotonating a chemical compound out of the group consisting of: acetoacetic ester, malonic mononitrile, malonic acid dimethylester, malonic acid diethylester, acetylacetone, malonic acid dinitrile, acetone, diethylketone, methlethylketone, dibutylketone, 1,3-dithian, acetaldehyde, benzaldehyde, crotonaldehyde and butyraldehyde.
In particular:
R¹, R^1′, R², R³may be alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl which may be independently substituted, or
two of the moieties R¹, R^1′, R², R³may form a ring together with a hetero-atom to which they are bound. The ring may be saturated, unsaturated, substituted or unsubstitued. The chain may be interrupted by one or more hetero-atoms out of the group consisting of O, S, NH or N—C₁-C₄-alkyl.
The hetero aromatic cation may be a 5 or 6 membered ring comprising at least one N and if necessary one 0 and/or one S. The hetero aromatic cation may be substituted or unsubstituted and/or annelated. Preferably, the hetero aromatic cation is selected from the group consisting of:
wherein the moieties R may be one of the following:
R hydrogen, C₁-C₃₀-alkyl, C₃-C₁₂-cycloalkyl, C₂-C₃₀-alkenyl, C₃-C₁₂-cycloalkenyl, C₂-C₃₀-alkinyl, aryl or heteroaryl, wherein the latter 7 moieties may have one or more halogenic moiety and/or 1 to 3 moieties selected from the group consisting of C₁-C₆-alkyl, aryl, heteroaryl, C₃-C₇-cycloalkyl, halogen, OR^c, SR^c, NR^cR^d, COR^c, COOR^c, CO—NR^cR^d, wherein R^cand R^dmay be hydrogen, C₁-C₆-alkyl, C₁-C₆-halogenalkyl, cyclopentyl, cyclohexyl, phenyl, tolyl or benzyl;
R¹, R^1′, R², R³may be hydrogen, alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl or heteroaryl which may be independently substituted; or
two of the moieties R1, R1′, R2, R3 may form a ring together with a hetero-atom to which they are bound. The ring may be saturated, unsaturated, substituted or unsubstitued. The chain may be interrupted by one or more hetero-atoms out of the group consisting of O, S, NH or N—C₁-C₄-alkyl;
R⁴, R⁵, R⁶, R⁷, R⁸may be, independently of each other, hydrogen, halogen, nitro, cyano, OR^c, SR^c, NR^cR^d, COR^c, COOR^c, CO—NR^cR^d, C₁-C₃₀-alkyl, C₃-C₁₂-cycloalkyl, C₂-C₃₀-alkenyl, C₃-C₁₂-cycloalkenyl, aryl or heteroaryl, wherein the latter 6 moieties may comprise one or more halogenic moiety and/or 1 to 3 moieties selected out of the group consisting of C₁-C₆-alkyl, aryl, heteroaryl, C₃-C₇-cycloalkyl, halogen, OR^c, SR^c, NR^cR^d, COR^c, COOR^c, CO—NR^cR^d, wherein R^cand R^dR^dmay be, independently of each other, hydrogen, C₁-C₆-alkyl, C₁-C₆-halogenalkyl, cyclopentyl, cyclohexyl, phenyl, tolyl or benzyl; or
two neighboring moieties of the moieties R, R⁴, R⁵, R⁶, R⁷, R⁸, may form, together with an atom they are bound, a ring which may be unsaturated or aromatic, unsaturated or saturated, wherein the chain formed by the respective moieties may be interrupted by one or more hetero-atoms out of the group consisting of O, S, NH or N—C₁-C₄-alkyl;
R^e, R^f, R^g, R^hmay be, independently of each other, hydrogen, C₁-C₆-alkyl, aryl-, heteroaryl-, C₃-C₇-cycloalkyl, halogen, OR^c, SR^c, NR^cR^d, COOR^c, CO—NR^cR^dor COR^c, wherein R^c, R^d, may be, independently of each other, hydrogen, C₁-C₆-alkyl, C₁-C₆-halogenalkyl, cyclopentyl, cyclohexyl, phenyl, tolyl or benzyl; preferably for hydrogen, halogen, C₁-C₆-alkyl, in particular, hydrogen or C₁-C₆-alkyl.
According to an exemplary embodiment of the method of use of an ionic liquid the non-aromatic cation is a quaternary material. In particular, the quaternary material may be a quaternary salt. Alternatively, the non aromatic cation may comprise or may consist of protonated bases.
According to an exemplary embodiment of the method of use of an ionic liquid the gas is one out of the group consisting of: H₂O, HCN, H₂S, H₂Se, H₂Te, CO₂, CO, CS₂, COS, CF₂O, CF₂S, O₃, NO, NO₂, N₂O, N₂O₃, NOCl, NF₃, HNO₂, HNO₃, RCOR′, RCOH, RCOOH, CF₃SO₃H, CF₃COOH, RCOOR′, ROH, ROR (including cyclic ethers like tetrahydrofuran), RSH, RSR (including cyclic thioethers like tetrahydrothiophen), ROCl, ROBr, RONH₂, RONHR', RONR′R″, RSO₂Cl, RSO₂Br, ROCN, RCON, RCN, HF, HCl, HBr, HI, SO₂, SO₃, NH₃, NH₂R, NHR′R″, NR′R″R′″, PH₃, PH₂R, PHR′R″, PR′R″R′″, BF₃, BCl₃, BBr₃, B₂H₆, BrF₃, ClF₃, ClF₅, ClCN, IF_S, AsH₃, CH₃F, CH₃Cl, CH₃Br, CH₃I, POCl₂, PSCl₂, PF_S, SF₄, SF₆, SO₂F₂, SO₂Cl₂, SOCl, H₂C═CHBr, H₂C═CHCl and ethylene oxide. In general, every gas or vapor having a multipole moment and which may be classified as an harmful substance, irritant, or toxic substance, e.g. (strong) acids, (strong) bases, may be sorbed by using a method according to an exemplary embodiment of the invention. In particular, the sorption process may be used to remove these gases or vapors from air which is inhaled or exhaled.
According to an exemplary embodiment of the method of use of an ionic liquid at least one of R, R′, R″ and/or R′″ is a moiety out of the group consisting of: C₁-C₈-alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl and heteroaryl. In particular, R, R′, R″ and/or R′″ may denote a moiety or radical which may be partially and/or independently substituted. For clarity reasons it should be mentioned that in this application the term C₁-C₈-alkyl or similar terms is an abbreviatory notation for C1-alkyl, C2-alkyl, . . . , up to C8-alkyl or similar terms.
According to an exemplary embodiment of the method of use of an ionic liquid the anion comprises a carbonate, an alkylcarbonate, an arylcarbonate, alkylcarbonate, carboxylate, a carbanion, and/or an aromatic compound. In particular, the carbonates may be alkaline metal carbonates, alkaline earth metal carbonates, quaternary tetraalkylammonium carbonates, quaternary tetraalkylphosphonium carbonates, hydrogencarbonate, and/or arylcarbonate, for example. In particular, the arylcarbonate may be phenylcarbonate or benzylcarbonate, for example.
According to an exemplary embodiment of the method of use of an ionic liquid the anion comprises at least one polar group.
In particular, the polar group may be formed by an acetate, a sulfonate, a sulfate, a carbonate, and/or a malonate compound. Furthermore, it should be noted that the anion may be polar. In particular, the anion may be formed by a small ion having a high charge density or by an ion, carrying a functional group with a heteroatom with a high charge density e.g. O, N, F.
According to an exemplary embodiment of the method of use of an ionic liquid the cation is a quaternary or protonated cation out of the group consisting of ammonium, phosphonium, sulfonium, piperidinium, pyrrolidinium and morpholinium.
According to an exemplary embodiment of the method of use of an ionic liquid the cation is one out of the group consisting of trialkylmethylammonium, tetramethylammonium, triethylmethylammonium, tributylmethylammonium, and trioctylmethylammonium, trialkylammonium, trimethylammonium, triethylammonium, tributylammonium, and trioctylammonium. In particular, the trialkylmethylammonium may be a C₁-C₁₀-trialkylmethylammonium.
According to an exemplary embodiment of the method of use of an ionic liquid the cation is one out of the group consisting of tetramethylammonium, triethylmethylammonium, tributylmethylammonium, and trioctylmethylammonium.
According to an exemplary embodiment of the method of use of an ionic liquid the anion can be written in the form [RCO₂ ⁻], wherein [RCO₂ ⁻] is one out of the group consisting of carboxylate, formiate, acetate, propionate, butyrate, benzoate, and salicylate.
According to an exemplary embodiment of the method of use of an ionic liquid the anion can be written in the form [RCO₂ ⁻], wherein [RCO₂ ⁻] is a carboxylate and wherein R is a radical out of the group consisting of C₁-C₃₀-alkyl, C₃-C₁₂-cycloalkyl, C₂-C₃₀-alkenyl, C₃-C₁₂-cycloalkenyl, C₂-C₃₀-alkinyl, aryl and heteroaryl. In particular, the moiety or radical R may comprise or include one or more halogen radicals.
According to an exemplary embodiment of the method of use of an ionic liquid the anion can be written in the form [RCO₂ ⁻], wherein [RCO₂] is a carboxylate wherein R represents one to three radicals out of the group consisting of, C₁-C₆-alkyl, aryl, heteroaryl, C₃-C₇-cycloalkyl, halogen, cyanide, ORc, SRc, NRcRd, CORc, COORc, CO—NRcRd, wherein Rc and/or Rd, is one of the group consisting of hydrogen, C₁-C₆-alkyl, C₁-C₆-halogenalkyl, cyclopentyl, cyclohexyl, phenyl, tolyl, and benzyl.
According to an exemplary embodiment of the method of use of an ionic liquid the gas is CO₂.
Summarizing, according to an exemplary aspect of the invention, a method of use is provided which uses an ionic liquid having a non-aromatic cation to sorb gases having an electric multipole moment. The gas may in particular be CO₂while the ionic liquid may be an organic salt having a melting temperature of below 200° C., preferably below 100° C. The organic salts may be quaternary salts having a generic formula of: [K⁺][RCO₂]. The described method of use may be in particular useful for all processes in which CO₂shall be removed as pure substance or from a gas or vapor mixture independent of whether CO₂is a main or secondary component, a process gas, or a working medium. Some exemplary applications may be the use in a heat pump or refrigerator based on ionic liquid/CO₂as working media, or removing of CO₂out of recovery gas, synthesis gas, water gas, inhaled air, and exhaled air. The removing out of inhaled/exhaled air may be in particular useful in the field of aerospace, submarines, or building services engineering wherein the very low vapor pressure if the ionic liquid may be advantageous since the ionic liquid may not evaporate into the air. Furthermore, it may be possible to use ionic liquids which selectively remove CO₂while do not remove water or water vapor, i.e. hydrophobic ionic liquids may be used. Another possible application may be the purification of CO₂and/or non-pressurized storing of CO₂, since the ionic liquid forms a complex bound with the quadrupolaric CO₂which complex bound may be broken by heating, microwave, ultrasonic wave, or by adding bipolar solvents, e.g. water, alcohol, etc. In general, every gas or vapor having a multipole moment and which may be classified as an harmful substance, irritant, or toxic substance, e.g. (strong) acids, (strong) bases, may be sorbed by using a method according to an exemplary embodiment of the invention. In particular, the sorption process may be used to remove these gases or vapor from air which is inhaled or exhaled, e.g. for purifying breathable air.
The aspects defined above and further aspects of the invention are apparent from the examples of embodiment to be described hereinafter and are explained with reference to these examples of embodiment. It should be noted that features described in connection with one exemplary embodiment or exemplary aspect may be combined with other exemplary embodiments and other exemplary aspects.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be described in more detail hereinafter with reference to examples of embodiment but to which the invention is not limited.

FIG. 1 schematically illustrates a heat pump.

FIG. 2 schematically illustrates a test arrangement for measuring a gas sorption.

FIG. 3 schematically illustrates a test arrangement for measuring equilibrium curves.

FIG. 4 illustrates equilibrium curves for monoethanolamine.

FIG. 5 illustrates equilibrium curves for choline carbonate.

DESCRIPTION OF EMBODIMENTS

The illustration in the drawing is schematically.
FIG. 1 schematically shows a heat pump which may use a process according to an exemplary embodiment, i.e. a process which may be based on pair of working media comprising CO₂and an ionic liquid comprising a non-aromatic ionic liquid.
In particular, FIG. 1 shows a heat pump 100 having an absorber 101, including the pair of working media, e.g. CO₂and the ionic liquid, wherein the ionic liquid acts as a sorbent and CO₂is the sorbat. The mixture is transmitted via a pump 102 to a heat exchanger 103 a in which the mixture absorbs heat or releases heat. After the heat exchanger the mixture is transmitted to a settler 104 in which at least a partially seperation of the mixture into a sorbent rich phase and a sorbat rich phase is performed. The sorbant rich phase is transferred to transferred trough a second heat exchanger 103 b and a restrictor 105 a into a evaporizer 106. In the evaporizer 106 the sorbat at least partially evaporates out of the sorbat rich phase which is then introduced back into the absorber 101. Optionally, the sorbat rich phase may be passed through another heat exchanger, e.g. heat exchanger 103 b, before it is introduced into the absorber. The sorbent richt phase is transferred from the settler 104 to the absorber 101 via a second restrictor 105 b in which it is brought back to the pressure level of the absorber 100. Optionally the sorbent rich phase may be passed through another heat exchanger, e.g. heat exchanger 103 a, before it is introduced into the second restrictor 105 b.
The described heat exchanger is only an example for a device using a method of use according to an exemplary embodiment of the invention. A plurality of embodiments may become apparent for a person skilled in the art. For example, a ionic liquid having a non-aromatic cation may be used in a open device, i.e. a device which does not include the ionic liquid in a closed loop, in order to enable the sorption of a gas having an electric multipole moment.
In the following some experimental results are described showing the ability of ionic liquid to absorb CO₂.
FIG. 2 schematically shows a fluid tank 200 used as a heat reservoir in order to provide a constant temperature selectable in the range between 25° C. and 80° C. A vessel or vial 201 having a volume of about 20 ml is placed in the tank, wherein the vial is filled with CO₂at a partial pressure of the enviromental pressure, e.g. atmospheric pressure of about 1000 hPa. Additionally, a CO₂sorbing fluid is injected 202 into the vial. The sorption of the CO₂is determined by measuring the decrease of the pressure in the vial by a digital manometer 203 which is connected to a computer. The speed of the pressure decrease is an indicator of the reaction kenetics and the total decrease of the pressure is an indicator for the total CO₂sorption. The tests were performed at two temperatures 25° C. and 80° C., wherein at the higher temperature a smaller amount of CO₂may be desirable since this may be an indicator for an estimation of the ability of the fluid to release the CO₂. For testing several ionic liquids are injected and compared to a reference sample, wherein an aqueous solution (30%) of monoethanolamine is used. In particular, the resulting parameter was the equilibrium concentration at constant reduced pressure, i.e. the pressure reached in the vial, and at the set temperature, wherein the result was calculated in mol_gasper mol_IL, wherein the index gas denotes CO₂and the index IL denotes ionic liquid. The equilibrium concentration were calculated by the following formular:
$\frac{pressure decrease [hPa] \cdot 0.02145 [l]}{83.145 \cdot temp [K]} / \frac{mass of {CO}_{2} [g]}{molar mass [g / mol]}$
wherein 0.02145 is the volume of the vial and 83.145 is the gas constant in the used units.
The following results were achieved:


				pressure
		conc.	T	decrease	time	charging
name	solvent	[%]	[° C.]	[hPa]	[min]	[mol_CO2/mol_IL]

TBMP-		100	25	332	4000	0.08
acetate
TBMP-		100	80	342	3160	0.08
acetate
TEMA-	H₂O	70	25	495	2400-5000	0.1
acetate
TEMA-	H₂O	70	80	130	2400	0.03
acetate
TOMA-		100	25	448	2500	0.19
acetate
TOMA-		100	80	122	1000	0.05
acetate
MEA	H₂O	30	25	679	250	0.12
MEA	H₂O	30	80	440	130	0.08

wherein:
TBMP denotes tributyl methyl phosphonium,
TEMA denotes triethyl methyl ammonium,
TOMA denotes trioctyl methyl ammonium, and
MEA denotes monoethanolamine.

As can be seen the acetate anion may be responsible for a high CO₂sorption, while similar sorption amounts may be achievable by cations having different structures.
FIG. 3 schematically illustrates a test arrangement 300 for measuring equilibrium curves. In particular, FIG. 3 shows an equilibrium cell comprising three vessels 301, 302 and 303 each closed by a respective frit in order to ensure a good mass transfer between the gas, e.g. CO₂and the sorbing fluid. The vessels are interconnected by flexible plastic tubes 304 and 305 having non-return valves. The vessels are placed in a heat reservoir 306 to ensure a constant temperature which can be controlled by using an electric heating 307. The heat reservoir is covered by a cover or lid 308 in order to ease the temperature control. A container or condenser 309 including silica gel is implemented downstream of the equilibrium cell wherein the silica gel is used to dry the generated gas which is then analyzed. Additionally, an input amount or volume to the equilibrium cell is controlled or regulated by using a rotameter 310.
FIG. 4 illustrates equilibrium curves for monoethanolamine. In particular, FIG. 4 shows the partial pressure p_CO2versus the CO₂loading for 60° C. and 80° C. for an aqueous solution (30%) of monoethanolamine. For each temperature a respective curve is approximated based on measurements, wherein a first curve 401 approximates the equilibrium curve for 80° C. while a second curve 402 approximates the equilibrium curve for 60° C. The values generated for MEA are comparable with the data published in literature, known to the expert.
FIG. 5 illustrates equilibrium curves for choline carbonate. In particular, FIG. 5 shows values for the partial pressure p_CO2versus the CO₂loading for six different temperatures 40° C., 60° C., 80° C., 90° C., 100° C., and 110° C. for an aqueous solution (60%) of choline carbonate. Additionally, to the measured values fits for the different temperatures are shown in FIG. 5 as well. In particular, graph 501 shows the fit for 40° C., graph 502 shows the fit for 60° C., graph 503 shows the fit for 80° C., graph 504 shows the fit for 90° C., graph 505 shows the fit for 100° C., and graph 506 shows the fit for 110° C.
Furthermore, an experiment concerning the influence of water on the CO₂sorption was performed. TEMA acetate having a water amount of 10% was used as an ionic liquid. TEMA acetate was introduced for four days into a CO₂atmosphere having a pressure of 600 hPa at a temperature of 80° C. In one case the TEMA acetate comprised included a surplus of water while in the other case no water was added. The water content of the sample including water increased from 10% to 35% while the sample without water increased only from 10% to 15%. After the four days acid was added to the two samples which lead to a clear generation of foam or gas in the sample without water, while the reaction of the probe with water was less intense. Thus, the water may lead to a reduced CO₂sorption of the ionic liquid.
In the following two examples will be described wherein trioctylmethylammonium (TOMA)-acetylacetonate or -acetate is used to sorp a gas having an electric multipole moment.

Example 1

Sorption of Hydrogen Sulphide

The experiment was performed at room temperature and a vapor pressure equilibrium of 338 hPa. A beaded bottle is flushed with 120 ml of hydrogen sulphide by using two needles. One of the needles is connected to a manometer having a resolution of 1 hPa. Subsequently 1 ml of TOMA-acetate is injected into the bottle by using one of the needles, wherein the TOMA-acetate was preheated by a hairdryer in order to reduce the viscosity. After 30 minutes of stirring by using a magnetic stir bar a constant reduction of the pressure of 622 hPa was observed. This pressure reduction corresponds to a molar ratio of 0.26 moI_H2S/mol_ILat an equilibrium pressure of 338 hPa. For comparison, a 30% aqueous solution of monoethanolamine provides, under the same conditions, a pressure reduction of 651 hPa which corresponds to a molare ratio of 0.11 mol_H2S/mol_Lat an equilibrium pressure of 309 hPa.

Example 2

Sorption of Carbon Dioxide

The experiment was performed at room temperature and a vapor pressure equilibrium of 523 hPa. A beaded bottle is flushed with 120 ml of carbon dioxide by using two needles. One of the needles is connected to a manometer having a resolution of 1 hPa. Subsequently 1 ml of TOMA-acetylacetonate is injected into the bottle by using one of the needles, wherein the TOMA-acetylacetonate was preheated by a hairdryer in order to reduce the viscosity. After 30 minutes of stirring by using a magnetic stir bar a constant reduction of the pressure of 437 hPa was observed. This pressure reduction corresponds to a molar ratio of 0.18 mol_CO2/mol_ILat an equilibrium pressure of 523 hPa. For comparison, a 30% aqueous solution of monoethanolamine provides, under the same conditions, a pressure reduction of 670 hPa which corresponds to a molare ratio of 0.12 mol_CO2/mol_Lat an equilibrium pressure of 290 hPa.
Finally, it should be noted that the above-mentioned embodiments illustrate rather than limit the invention, and that those skilled in the art will be capable of designing many alternative embodiments without departing from the scope of the invention as defined by the appended claims. In the claims, any reference signs placed in parentheses shall not be construed as limiting the claims. The word “comprising” and “comprises”, and the like, does not exclude the presence of elements or steps other than those listed in any claim or the specification as a whole. The singular reference of an element does not exclude the plural reference of such elements and vice-versa. In a device claim enumerating several means, several of these means may be embodied by one and the same item of software or hardware. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage.

Claims

1. A method comprising:

using an ionic liquid for sorption of a gas having an electric multipole moment, wherein the ionic liquid comprises an anion and a non-aromatic cation.

2. The method according to claim 1, wherein the non-aromatic cation is an aliphatic cation.

3. The method according to claim 1, wherein the non-aromatic cation is a quaternary material.

4. The method according to claim 1, wherein the gas is one out of the group consisting of:

H₂O, HCN, H₂S, H₂Se, H₂Te, CO₂, CO, CS₂, COS, CF₂O, CF₂S, O₃, NO, NO₂, N₂O, N₂O₃, NOCl, NF₃, HNO₂, HNO₃, RCOR′, RCOH, RCOOH, CF₃SO₃H, CF₃COOH, RCOOR′, ROH, ROR, RSH, RSR, ROCl, ROBr, RONH₂, RONHR′, RONR′R″, RSO₂Cl, RSO₂Br, ROCN, RCON, RCN, HF, HCl, HBr, HI, SO₂, SO₃, NH₃, NH₂R, NHR′R″, NR′R″R′″, PH₃, PH₂R, PHR′R″, PR′R″R′″, BF₃, BCl₃, BBr₃, B₂H₆, BrF₃, ClF₃, ClF₅, ClCN, IF₅, AsH₃, CH₃F, CH₃Cl, CH₃Br, CH₃I, POCl₂, PSCl₂, PF₅, SF₄, SF₆, SO₂F₂, SO₂Cl₂, SOCl, H₂C═CHBr, H₂C═CHCl and ethylene oxide.

5. The method according to claim 4, wherein at least one of R, R′, R″ and/or R′″ is a moiety out of the group consisting of:

C₁-C₈-alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, aryl and heteroaryl.

6. The method according to claim 1, wherein the anion comprises a carbonate, an alkylcarbonate, an arylcarbonate a carboxylate, a carbanion, and/or an aromatic compound.

7. The method according to claim 1: wherein the ionic liquid satisfies the generic formula [Q⁺][A⁻], wherein the anion is described by one of the following structures:

8. The method according to claim 1, wherein the ionic liquid satisfies the generic formula [Q⁺]_a[A^a-], wherein [A^a-] with the charge a-, is selected out of the group consisting of:

dialkyl ketones, dialkyl-1,3-diketones, alkyl-β-keto esters, terminal alkines, linear or cyclic 1,3-thioethers, dialkyl phosphonates, dialkyl malonic acid esters, β-cyano carbonic acids and their respective alkylesteres, β-alkoxy carbonic acids and their respective alkylesters, β-cyano nitriles, cyclopentadiene (substituted if necessary), trialkylimines, dialkylimines, diaryl ketones, alkyl-aryl-ketones, diaryl-1,3-diketones, alkyl-aryl-1,3-diketones, β-aryloxy carbonic acids and their respective alkylesters, β-aryloxy carbonic acids and their respective arylesters, aryl-β-ketoesters, diarylphosphonates, alkyl-aryl-phosphonates, diaryl malonic acid esters, alkyl-aryl-malonic acid esters, β-cyano carbonic acids arylesters and arylimines.

9. The method according to claim 1, wherein the ionic liquid satisfies the generic formula [Q⁺]_a[A^a-], wherein [A^a-] is a carbanion formed by deprotonating a chemical compound out of the group consisting of:

acetoacetic ester, malonic mononitrile, malonic acid dimethylester, malonic acid diethylester, acetylacetone, malonic acid dinitrile, acetone, diethylketone, methlethylketone, dibutylketone, 1,3-dithian, acetaldehyde, benzaldehyde, crotonaldehyde and butyraldehyde.

10. The method according to claim 1, wherein the anion comprises at least one polar group.

11. The method according to claim 1, wherein the cation is a quaternary or protonated cation out of the group consisting of:

ammonium, phosphonium, sulfonium, piperidinium, pyrrolidinium, and morpholinium.

12. The method according to claim 1, wherein the cation is one out of the group consisting of:

trialkylmethylammonium, tetramethylammonium, triethylmethylammonium, tributylmethylammonium, trio ctylmethylammonium trialkylammonium, trimethylammonium, triethylammonium, tributylammonium, and trioctylammonium.

13. The method according to claim 1, wherein the cation is one out of the group consisting of:

tetramethylammonium, triethylmethylammonium, tributylmethylammonium, and trio ctylmethylammonium.

14. The method according to claim 1, wherein the anion is written in the form [RCO₂ ⁻], wherein [RCO₂ ⁻] is one out of the group consisting of:

carboxylate, formiate, acetate, propionate, butyrate, benzoate, and salicylate.

15. The method according to claim 1, wherein the anion is written in the form [RCO₂ ⁻], wherein [RCO₂ ⁻] is a carboxylate wherein R is a radical out of the group consisting of:

C₁-C₃₀-alkyl, C₃-C₁₂-cycloalkyl, C₂-C₃₀-alkenyl, C₃-C₁₂-cycloalkenyl, C₂-C₃₀-alkinyl, aryl and heteroaryl.

16. The method according to claim 1, wherein the anion is written in the form [RCO₂], wherein [RCO₂ ⁻] is a carboxylate wherein R represents one to three radicals out of the group consisting of:

C₁-C₆-alkyl, aryl, heteroaryl, C₃-C₇-cycloalkyl, halogen, cyanide, ORc, SRc, NRcRd, CORc, COORc, CO—NRcRd,

wherein Rc and/or Rd, is one of the group consisting of:

hydrogen, C₁-C₆-alkyl, C₁-C₆-halogenalkyl, cyclopentyl, cyclohexyl, phenyl, tolyl, and benzyl.

17. The method according to claim 1, wherein the gas is CO₂.

18. The method according to claim 17, wherein CO₂is sorbed from a medium which is selected out of the group consisting of:

recovery gas, synthesis gas, water gas, inhaled air, and exhaled air.

19. A device for sorption of a gas having an electric multipole moment, the device comprising:

a reservoir of an ionic liquid comprising an anion and a non-aromatic cation.

20. The device according to claim 19, wherein the device is a heat pump, and wherein the heat pump comprises a circuit including CO₂and the ionic liquid comprises an anion and a non-aromatic cation as working media.

21. A method comprising:

using an ionic liquid for sorption of a gas having an electric multipole moment, wherein the ionic liquid comprises a carbanion and a cation.

22. The method according to claim 21, wherein the ionic liquid satisfies the generic formula [Q⁺]_a[A^a-],

wherein [Q]⁺ is one out of the group consisting of quaternary ammonium cation [R^1′R¹R²R³N]⁺, phosphonium [R^1′R¹R²R³P]⁺, sulfonium [R^1′R¹R²S]⁺ and a hetero aromatic cation.