WO2007057235A2 - Lösungen von cellulose in ionischen flüssigkeiten - Google Patents
Lösungen von cellulose in ionischen flüssigkeiten Download PDFInfo
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- WO2007057235A2 WO2007057235A2 PCT/EP2006/061422 EP2006061422W WO2007057235A2 WO 2007057235 A2 WO2007057235 A2 WO 2007057235A2 EP 2006061422 W EP2006061422 W EP 2006061422W WO 2007057235 A2 WO2007057235 A2 WO 2007057235A2
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- 0 CCCC1(*)N(C)NN(*)C1* Chemical compound CCCC1(*)N(C)NN(*)C1* 0.000 description 7
- XDTMQSROBMDMFD-UHFFFAOYSA-N C1CCCCC1 Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B1/00—Preparatory treatment of cellulose for making derivatives thereof, e.g. pre-treatment, pre-soaking, activation
- C08B1/003—Preparation of cellulose solutions, i.e. dopes, with different possible solvents, e.g. ionic liquids
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- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
- D21C3/04—Pulping cellulose-containing materials with acids, acid salts or acid anhydrides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21C—PRODUCTION OF CELLULOSE BY REMOVING NON-CELLULOSE SUBSTANCES FROM CELLULOSE-CONTAINING MATERIALS; REGENERATION OF PULPING LIQUORS; APPARATUS THEREFOR
- D21C3/00—Pulping cellulose-containing materials
- D21C3/02—Pulping cellulose-containing materials with inorganic bases or alkaline reacting compounds, e.g. sulfate processes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2301/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2301/02—Cellulose; Modified cellulose
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/54—Improvements relating to the production of bulk chemicals using solvents, e.g. supercritical solvents or ionic liquids
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2989—Microcapsule with solid core [includes liposome]
Definitions
- the present invention relates to a solution of cellulose and an ionic liquid as solvent, process for their preparation and their use.
- Cellulose is a very versatile raw material.
- cellulose is the most important constituent of the fiber raw materials, in particular cotton.
- Cellulose can be used unchanged or after physical or chemical treatment. For the two latter cases, it is advantageous if cellulose is present in a solvent in as completely dissolved form as possible. However, cellulose is insoluble in most solvents.
- cellulose is soluble as a copper-chelate complex. By precipitation of the cellulose, the so-called regenerated cellulose can be obtained.
- copper solutions are poorly suited to serve as a solvent for cellulose in their physical or chemical treatment.
- US-A 1,943,176 describes the dissolution of cellulose in benzylpyridinium chloride.
- Benzylpyridinium chloride which is an example of an ionic liquid, is a salt which, even at comparatively low temperatures, is present in molten form and thus as a liquid.
- Ionic liquids gain as a solvent, e.g. in carrying out chemical reactions, increasingly important.
- Ionic liquids already in liquid state at room temperature are described, for example, by KN Marsh et al., Fluid Phase Equilibria 219 (2004), 93-98 and JG Huddieston et al., Green Chemistry 2001, 3, 156-164.
- DE-A 102 02 838 describes the use of ionic liquids for the separation of acids from chemical mixtures.
- ionic liquids should consist of cations having a quaternary ammonium ion, which should be quaternized by alkyl groups, especially methyl.
- the object is achieved by a solution comprising cellulose and an ionic liquid containing anions and cations as solvent, wherein the cations have at least one atom selected from the group consisting of nitrogen, oxygen, sulfur and phosphorus, which is present in protonated form.
- the protonation can take place on one or more identical or different heteroatoms (N, O, S, P).
- heteroatoms N, O, S, P
- other positive charges in the cations may be present, for example by alkylation of a nitrogen.
- the cations have at least one nitrogen atom present in protonated form as an ammonium cation.
- the cellulose to be dissolved may be derived, for example, from regenerated cellulose, fibrous cellulose, wood fibers, linter, cotton or paper.
- cellulose is completely dissolved at more than 1% by weight based on the total weight of the solution become. More preferably, more than 3% by weight, more preferably more than 5% by weight, and most preferably at least 7% by weight, based on the total weight of the solution, will be completely dissolved.
- cellulose based on the total weight of the solution can be completely dissolved.
- up to 25% by weight of cellulose based on the total weight of the solution can be completely dissolved.
- Particularly suitable for certain applications are solutions in which cellulose with up to 15 wt .-% are completely dissolved.
- Ionic liquids in the context of the present invention are preferably salts of the general formula
- n 1, 2, 3 or 4
- [A] + is a quaternary ammonium cation, an oxonium cation, a sulfonium cation or a phosphonium cation
- [Y] n ⁇ is a one- or two-membered cation -, tri- or tetravalent anion stands;
- [A 1 J + , [A 2 J + and [A 3 J + are independently selected from the groups mentioned for [A] + , [Y] n ⁇ has the meaning given under (A) and [M 1 J + , [M 2 J + , [M 3 J + monovalent metal cations, [M 4 J 2+ divalent metal cations and [M 5 J 3+ trivalent metal cations.
- the ionic liquids have a melting point of less than 180 ° C. Further preferably, the melting point is in a range of -50 ° C to 150 ° C, more preferably in the range of -20 ° C to 120 ° C and further more preferably less than 100 0 C.
- Such compounds may contain oxygen, phosphorus, sulfur or in particular nitrogen atoms, for example at least one nitrogen atom, preferably 1-10 nitrogen atoms, more preferably 1-5, most preferably 1-3 and especially 1-2
- Nitrogen atoms optionally, other heteroatoms such as oxygen,
- Sulfur or phosphorus atoms may be included.
- the nitrogen atom is a suitable carrier of the positive charge in the cation of the ionic liquid, of which in the
- a cation can first be generated by quaternization on the nitrogen atom of, for example, an amine or nitrogen heterocycle.
- the quaternization can be carried out by protonation of the nitrogen atom.
- salts with different anions are obtained.
- this can be done in a further synthesis step.
- the halide can be reacted with a Lewis acid to form a complex anion from halide and Lewis acid.
- replacement of a halide ion with the desired anion is possible. This can be done by adding a metal salt to precipitate the metal halide formed, via an ion exchanger, or by displacing the halide ion with a strong acid (to release the hydrohalic acid). Suitable methods are, for example, in Angew. Chem. 2000, 112, p. 3926-3945 and the literature cited therein.
- those compounds which contain at least one five- to six-membered heterocycle in particular a five-membered heterocycle, which has at least one nitrogen atom and optionally an oxygen or sulfur atom
- aromatic heterocycles are particularly preferred.
- Particularly preferred compounds are those which have a molecular weight below 1000 g / mol, very particularly preferably below 500 g / mol and in particular below 250 g / mol.
- radical R is hydrogen
- radicals R 1 to R 9 independently of one another are hydrogen, a sulfo group or a carbon-containing organic, saturated or unsaturated, acyclic or cyclic, aliphatic, aromatic or araliphatic, unsubstituted or interrupted by 1 to 5 heteroatoms or functional groups having 1 to 20 carbon atoms, wherein the radicals R 1 to R 9 , which in the abovementioned formulas (IV) are bonded to a carbon atom (and not to a heteroatom), additionally may also stand for halogen or a functional group; or
- two adjacent radicals from the series R 1 to R 9 together also for a divalent, carbon-containing organic, saturated or unsaturated, acyclic or cyclic, aliphatic, aromatic or araliphatic, unsubstituted or interrupted by 1 to 5 heteroatoms or functional groups radical or substituted 1 to 30 carbon atoms.
- the carbon-containing group contains heteroatoms, oxygen, nitrogen, sulfur, phosphorus and silicon are preferable.
- the radicals R 1 to R 9 are, in the cases in which these are attached in the abovementioned formulas (IV) to a carbon atom (and not to a heteroatom), also be bound directly via the heteroatom.
- Suitable functional groups are in principle all functional groups which may be bonded to a carbon atom or a heteroatom.
- -OH (hydroxy), 0 (especially as carbonyl group)
- - NH 2 (amino), NH (imino), -COOH (carboxy), -CONH 2 (carboxamide), -SO 3 H (sulfo) and -CN (cyano).
- Functional groups and heteroatoms can also be directly adjacent, so that combinations of several adjacent atoms, such as -O- (ether), -S- (thioether), -COO- (ester), -CONH- (secondary amide) or are (tertiary amide), with includes, for example, di- (CrC 4 alkyl) amino, d- C kyloxy 4 alkyloxycarbonyl or Ci -C 4 -alkyl - CONR. 1
- Halogens are fluorine, chlorine, bromine and iodine.
- radicals R 1 to R 9 are preferably each independently
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles substituted and / or interrupted by one or more oxygen and / or sulfur atoms and / or one or more substituted or unsubstituted imino C r Ci 8 alkyl;
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles substituted and / or interrupted by one or more oxygen and / or sulfur atoms and / or one or more substituted or unsubstituted imino C 2 -Ci 8- alkenyl;
- aryl optionally substituted by functional groups, aryl, alkyl, aryloxy, alkoxy, halogen, heteroatoms and / or heterocycles substituted C 6 -C 2 -aryl;
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles C r to Ci 8 alkyl is preferably 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, 3-methyl-3
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles is preferably phenyl, ToIyI, XyIyI, ⁇ -naphthyl, ß-naphthyl, 4- Diphenylyl, chlorophenyl, dichlorophenyl, trichlorophenyl, difluorophenyl, methylphenyl, dimethylphenyl, trimethylphenyl, ethylphenyl, dimethylphenyl, / so-propylphenyl, tert-butylphenyl, dodecylphenyl, methoxyphenyl, dimethoxyphenyl, ethoxyphenyl, hexyloxyphenyl, methylnaphthyl, isopropylnaphthyl , Chlorona
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles C 5 - to C 2 -cycloalkyl is preferably cyclopentyl, cyclohexyl, cyclooctyl, cyclododecyl,
- An optionally substituted by functional groups, aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles substituted five- to six-membered, oxygen, nitrogen and / or sulfur atoms containing heterocycle is preferably furyl, thiophenyl, pyrryl, Pyridyl, indolyl, benzoxazolyl, dioxolyl, dioxo, benzimidazolyl, benzthiazolyl, dimethylpyridyl, methylquinolyl, dimethylpyrryl, methoxyfuryl, dimethoxypyridyl or difluoropyridyl.
- Two adjacent radicals together form an unsaturated, saturated or aromatic, optionally substituted by functional groups, aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles and optionally substituted by one or more oxygen and / or sulfur atoms and / or one or more several substituted or unsubstituted imino groups interrupted ring, it is preferably 1, 3-propylene, 1,4-butylene, 1,5-pentylene, 2-oxa-1,3-propylene, 1-oxa-1,3- propylene, 2-oxa-1,3-propylene, 1-oxa-1,3-propenylene, 3-oxa-1, 5-pentylene, 1-aza-1,3-propenylene, 1-Ci-C 4 alkyl 1-aza-1, 3-propenylene, 1,4-buta-1,3-dienylene, 1-aza-1,4-buta-1,3-dienylene or 2-aza-1, 4-buta-1 ,
- radicals contain oxygen and / or sulfur atoms and / or substituted or unsubstituted imino groups
- the number of oxygen and / or sulfur atoms and / or imino groups is not restricted. As a rule, it is not more than 5 in the radical, preferably not more than 4, and very particularly preferably not more than 3.
- radicals contain heteroatoms, then between two heteroatoms there are generally at least one carbon atom, preferably at least two carbon atoms.
- radicals R 1 to R 9 are each independently
- Glycols, butylene glycols and their oligomers having 1 to 100 units and a hydrogen or a C 1 to C 8 alkyl end group such as, for example, R A O- (CHR B -CH 2 -O) n -CHR B -CH 2 - or R A O- (CH 2 CH 2 CH 2 CH 2 O) n -CH 2 CH 2 CH 2 CH 2 O- with R A and R B preferably hydrogen, methyl or ethyl and n preferably 0 to 3, in particular 3
- N 1 N-di-Cr to C6 alkyl-amino such as N, N-dimethylamino and N 1 N-diethylamino.
- the radicals R 1 to R 9 are independently hydrogen or C r to C 8 alkyl such as methyl, ethyl, 1-butyl, 1-pentyl, 1-hexyl, 1-heptyl, 1-octyl, for phenyl, for 2-hydroxyethyl, for 2-cyanoethyl, for 2- (methoxycarbonyl) ethyl, for 2- (ethoxycarbonyl) ethyl, for 2- (n-butoxycarbonyl) ethyl, for N, N-dimethylamino, for N, N -Diethylamino, for chlorine and for CH 3 O- (CH 2 CH 2 O) n - CH 2 CH 2 - and CH 3 CH 2 O- (CH 2 CH 2 O) n -CH 2 CH 2 - where n is 0 to 3.
- C r to C 8 alkyl such as methyl, ethyl, 1-butyl, 1-pentyl, 1-hexyl
- radicals R 1 to R 5 are methyl, ethyl or chlorine and the remaining radicals R 1 to R 5 are hydrogen; • R 3 is dimethylamino and the remaining radicals R 1 , R 2 , R 4 and R 5
- R 2 is carboxy or carboxamide and the remaining radicals R 1 , R 2 , R 4 and R 5 are hydrogen; or R 1 and R 2 or R 2 and R 3 is 1,4-buta-1,3-dienylene and the remaining radicals R 1 , R 2 , R 4 and R 5 are hydrogen; or R 1 and R 2 or R 2 and R 3 is 1,4-buta-1,3-dienylene and the remaining radicals R 1 , R 2 , R 4 and R 5 are hydrogen; or R 1 and R 2 or R 2 and R 3 is 1,4-buta-1,3-dienylene and the remaining
- R 1 , R 2 , R 4 and R 5 are hydrogen; and in particular those in which
- R 1 to R 5 are hydrogen; or • one of R 1 to R 5 is methyl or ethyl and the remaining radicals
- R 1 to R 5 are hydrogen.
- pyridinium ions (IVa) its called pyridinium, 2-methylpyridinium, 2-ethylpyridinium, 5-ethyl-2-methylpyridinium and 2-methyl-3-ethyl-pyridinium.
- R 1 to R 4 are hydrogen
- radicals R 1 to R 4 are methyl or ethyl and the remaining radicals R 1 to R 4 are hydrogen.
- R 1 is hydrogen, methyl or ethyl and R 2 to R 4 are independently hydrogen or methyl; or
- R 1 is hydrogen, methyl or ethyl
- R 2 and R 4 are methyl and R 3
- R 1 is hydrogen, methyl or ethyl and R 2 to R 4 are independent of one another
- R 1 is hydrogen, methyl or ethyl, R 2 and R 4 are methyl and R 3 is hydrogen;
- R 1 to R 4 are methyl
- R 1 to R 4 are methyl hydrogen.
- imidazolimions (IVe) which may be mentioned are 1-methylimidazolium, 1-ethylimidazolium, 1-n-butylimidazolium, 1-n-octylimidazolium, 1-n-dodecylimidazolium, 1-n-tetradecylimidazolium, 1-n- Hexadecylimidazolium, 1,2-dimethylimidazolium, 1,4-dimethylimidazolium, 2-methylimidazolium, 3-methylimidazolium, 3-ethylimidazolium, 3-n-butylimidazolium, 3-octylimidazolium, 4-methylimidazolium, 2-ethylimidazolium, 1-vinylimidazolium, in-octyl-4-methylimidazolium and 1, 4,5-trimethylimidazolium.
- R 1 is hydrogen, methyl or ethyl and R 2 to R 4 are independent of one another
- R 1 to R 4 are independently hydrogen or methyl.
- pyrazolium ions are pyrazolium and 1,4-dimethylpyrazolium.
- R 1 to R 6 are hydrogen or methyl.
- R 1 is hydrogen, methyl, ethyl or phenyl and R 2 to R 6 are independently hydrogen or methyl.
- R 1 and R 2 are independently hydrogen, methyl, ethyl or phenyl and R 3 to R 6 are independently hydrogen or methyl.
- Very particularly preferred as Imidazoliniumionen (IVI) are those in which
- R 1 and R 2 are independently hydrogen, methyl, ethyl, 1-butyl or
- R 3 and R 4 are independently hydrogen, methyl or ethyl, and R 5 and R 6 are independently hydrogen or methyl.
- R 1 and R 2 are independently hydrogen, methyl or ethyl and R 3 to R 6 are independently hydrogen or methyl.
- R 1 to R 3 are independently hydrogen, methyl or ethyl and R 4 to R 6 are independently hydrogen or methyl.
- Very particular preference is given to using thiazolium ions (IVo) or (IVo ') and oxazolium ions (IVp) as those in which
- R 1 is hydrogen, methyl, ethyl or phenyl and R 2 and R 3 are independently hydrogen or methyl.
- R 1 and R 2 are independently hydrogen, methyl, ethyl or phenyl and R 3 is hydrogen, methyl or phenyl.
- R 1 is hydrogen, methyl or ethyl and R 2 and R 3 are independent of each other
- R 2 and R 3 together are 1, 4-buta-1,3-dienylene.
- Very particularly preferred pyrrolidinium ions are those in which • R 1 is hydrogen, methyl, ethyl or phenyl and R 2 to R 9 are independently hydrogen or methyl.
- R 1 and R 4 are independently hydrogen, methyl, ethyl or phenyl and R 2 and R 3 and R 5 to R 8 are independently hydrogen or methyl.
- R 1 to R 3 are independently C r to Ci 8 alkyl
- R 1 and R 2 together are 1,5-pentylene or 3-oxa-1, 5-pentylene and R 3 is d-Cis-alkyl, 2-hydroxyethyl or 2-cyanoethyl.
- Examples of the tertiary amines from which the quaternary ammonium ions of the general formula (IVu) are derived by quaternization with the radical R mentioned are diethyl-n-butylamine, diethyl-tert-butylamine, diethyl-n-pentylamine, diethylhexylamine, Diethyloctylamine, diethyl (2-ethylhexyl) amine, di-n-propylbutylamine, di-n-propyl-n-pentylamine, di-n-propylhexylamine, di-n-propyloctylamine, di-n-propyl (2-ethyl - hexyl) amine, di-isopropylethylamine, di-iso-propyl-n-propylamine, di-isopropyl-butylamine, di-isopropylpentylamine, di-is
- Preferred tertiary amines are di-iso-propylethylamine, diethyl-tert-butylamine, diisopropyl-propylamine, di-n-butyl-n-pentylamine, N, N-di-n-butylcyclohexylamine and tertiary amines of pentyl isomers.
- Particularly preferred tertiary amines are di-n-butyl-n-pentylamine and tertiary amines of pentyl isomers.
- Another preferred tertiary amine having three identical residues is triallylamine.
- R 1 to R 5 are methyl.
- R 1 and R 2 are independently methyl, ethyl, 1-butyl or 1-octyl and R 3 is hydrogen, methyl, ethyl, acetyl, -SO 2 OH or -PO (OH) 2 ;
- R 1 is methyl, ethyl, 1-butyl or 1-octyl
- R 2 is a -CH 2 -CH 2 -OR 4 group and R 3 and R 4 independently of one another are hydrogen, methyl, ethyl, acetyl,
- R 1 is a -CH 2 -CH 2 -OR 4 group
- R 2 is a -CH 2 -CH 2 -OR 5 group
- R 3 to R 5 are independently hydrogen, methyl, ethyl, acetyl, -SO 2 are OH or -PO (OH) 2 .
- Particularly preferred cholinium ions are those in which R 3 is selected from hydrogen, methyl, ethyl, acetyl, 5-methoxy-3-oxa-pentyl, 8-methoxy-3,6-dioxo-octyl, 11-methoxy 3,6,9-trioxa undecyl, 7-methoxy-4-oxa-heptyl, 11-methoxy-4,8-dioxa undecyl, 15-methoxy-4,8,12-trioxa-pentadecyl, 9-methoxy 5-oxa-nonyl, 14-methoxy-5,10-oxa-tetradecyl, 5-ethoxy-3-oxa-pentyl, 8-ethoxy-3,6-dioxo-octyl, 11-ethoxy-3,6,9- trioxa-undecyl, 7-ethoxy-4-oxa-hept
- R 1 to R 3 are independently of one another C 1 -C 8 -alkyl, in particular butyl, isobutyl, 1-hexyl or 1-octyl.
- the pyridinium ions, pyrazolinium, pyrazolium ions and imidazolinium and imidazolium ions are preferable. Also preferred are ammonium ions.
- the metal cations [M 1 J + , [M 2 J + , [M 3 J + , [M 4 J 2+ and [M 5 J 3+ ) mentioned in formulas (IIIa) to (MIj) are generally to metal cations of the 1st, 2nd, 6th, 7th, 8th, 9th, 10th, 11th, 12th and 13th group of the periodic table.
- Suitable metal cations are, for example, Li + , Na + , K + , Cs + , Mg 2+ , Ca 2+ , Ba 2+ , Cr 3+ , Fe 2+ , Fe 3+ , Co 2+ , Ni 2+ , Cu 2 + , Ag + , Zn 2+ and Al 3+ .
- the anion [Y] n of the ionic liquid is for example selected from
- R b is -O 2 S SO 2 -R 0
- M is a metal and Hal is fluorine, chlorine, bromine or iodine, q and r are all positive numbers and indicate the stoichiometry of the complex and s is an integer positive number indicating the charge of the complex;
- R a , R b , R c and R d are each independently hydrogen, C 1 -C 30 -alkyl, optionally interrupted by one or more non-adjacent oxygen and / or sulfur atoms and / or one or more substituted or unsubstituted imino groups C 2 -C 8 alkyl, C 6 -C 4 aryl, C 5 -C 2 cycloalkyl or a five- to six-membered, oxygen-, nitrogen- and / or sulfur-comprising heterocycle, where two of them together form an unsaturated, form saturated or aromatic, optionally interrupted by one or more oxygen and / or sulfur atoms and / or one or more unsubstituted or substituted imino groups ring, said radicals each additionally by functional groups, aryl, alkyl, aryloxy, alkoxy, halogen, Heteroatoms and / or heterocycles may be substituted.
- aryl, alkyl, aryloxy, alkyloxy, halogen, heteroatoms and / or heterocycles C r Ci 8 alkyl for example methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, tert-butyl , Pentyl, hexyl, heptyl, octyl, 2-ethylhexyl, 2,4,4-trimethylpentyl, decyl, dodecyl, tetradecyl, he-decyl, octadecyl, 1,1-dimethylpropyl, 1,1-dimethylbutyl, 1,1,3,3 Tetramethylbutyl, benzyl, 1-phenylethyl, ⁇ , ⁇ -dimethylbenzyl, benzhydryl, p-tolylmethyl, 1- (p-butyl)
- radicals can be taken together, for example, as fused building blocks, 1,3-propylene, 1,4-butylene, 2-oxa-1,3-propylene, 1-oxa-1,3-propylene, 2 oxa-1,3-propenylene, 1-aza-1,3-propenylene, 1-C r C 4 alkyl-1-aza-1, 3-propenylene, 1,4-buta-1,3- dienylene, 1-aza-1,4-buta-1,3-dienylene or 2-aza-1, 4-buta-1,3-dienylene mean.
- the number of non-adjacent oxygen and / or sulfur atoms and / or imino groups is basically not limited, or is automatically limited by the size of the remainder or of the ring building block. As a rule, it is not more than 5 in the respective radical, preferably not more than 4 or very particularly preferably not more than 3. Furthermore, at least one, preferably at least two, carbon atoms (e) are generally present between two heteroatoms.
- Substituted and unsubstituted imino groups may be, for example, imino, methylimino, iso-propylimino, n-butylimino or tert-butylimino.
- the term "functional groups” are understood to be for example the following: carboxy, carboxamide, hydroxy, di (CrC 4 alkyl) amino, -C 4 - alkyloxycarbonyl, cyano or C r C 4 alkoxy
- Ci to C. 4- alkyl methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl or tert-butyl.
- C 6 -C 4 -aryl substituted by functional groups are, for example, phenyl, ToIyI, XyIyI, ⁇ -naphthyl, ⁇ -naphthyl, 4-diphenylyl, chlorophenyl, Dichlorophenyl, trichlorophenyl, difluorophenyl, methylphenyl, dimethylphenyl, trimethylphenyl, ethylphenyl, dimethylphenyl, isopropylphenyl, tert-butylphenyl, dodecylphenyl, methoxyphenyl, D-imethoxyphenyl, ethoxyphenyl, hexyloxyphenyl, methylnaphthyl, isopropylnaphthyl, chloronaph
- cyclopentyl cyclohexyl, cyclooctyl, cyclododecyl
- methylcyclopentyl dimethylcyclopentyl
- methylcyclohexyl dimethylcyclohexyl
- diethylcyclohexyl diethylcyclohexyl
- butylcyclohexyl methoxycyclohexyl
- Dimethoxycyclohexyl diethoxycyclohexyl
- butylthiocyclohexyl chlorocyclohexyl, dichlorocyclohexyl, dichlorocyclopentyl and a saturated or unsaturated bicyclic system such as norbornyl or norbornyl.
- a five- to six-membered oxygen, nitrogen and / or sulfur heterocycle is, for example, furyl, thiophenyl, pyryl, pyridyl, indolyl, benzoxazolyl, dioxolyl, dioxy, benzimidazolyl, benzthiazolyl, dimethylpyridyl, methylquinolyl, dimethylpyryl, methoxifuryl, dimethoxypyridyl, diflouropyridyl , Methylthiophenyl, isopropylthiophenyl or tert-butylthiophenyl.
- Preferred anions are selected from the group of halides and halogen-containing compounds, the group of carboxylic acids, the group of sulfates, sulfites and sulfonates and the group of phosphates.
- Preferred anions are chloride, bromide, iodide, SCN “ , OCN “ , CN “ , acetate, dC 4 alkyl sulfates, R a -COO " , R 3 SO 3 " , R a R b PO 4 " , methanesulfonates, tosylate, C r C 4 dialkyl phosphates, hydrogen sulfate or tetrachloroaluminate.
- Particularly preferred anions are Cl “ , CH 3 COO “ or CH 3 SO 3 " .
- Cations and anions are present in the ionic liquid.
- a proton or an alkyl radical is transferred from the cation to the anion. This creates two neutral molecules.
- the solution has a temperature of at most 180 0 C. More preferably, the solution of the present invention has a temperature of at most 160 ° C, more preferably at most 120 ° C, and most preferably at most 100 ° C.
- Another object of the present invention is a process for preparing a solution according to the invention comprising the steps
- the mixing is preferably carried out by stirring, shaking and / or with the aid of microwaves.
- the dissolution occurs within 3 days, more preferably within one day, and most preferably within 12 hours.
- Another object of the present invention is the use of a solution according to the present invention for the physical or chemical treatment of cellulose.
- the chemical treatment may include oxidation, reduction, pyrolysis, hydrolysis, isomerization, esterification, alkoxylation or copolymerization.
- filter paper (Blauband filter) are cut into pieces of about 1 cm 2 , mixed with 100 g of 1-methylimidazole hydrochloride and stirred at 95 ° C. After 72 hours, the paper has completely dissolved.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
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Abstract
Description
Claims
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN200680012598XA CN101160325B (zh) | 2005-04-15 | 2006-04-07 | 离子液体中的纤维素溶液 |
AU2006314736A AU2006314736B2 (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
NZ560914A NZ560914A (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids based upon imidazolium cations |
BRPI0609083-4A BRPI0609083A2 (pt) | 2005-04-15 | 2006-04-07 | solução, processo para preparar a mesma, e, uso de uma solução |
EA200701783A EA016748B1 (ru) | 2005-04-15 | 2006-04-07 | Раствор, содержащий целлюлозу и ионную жидкость, способ его получения и его применение для физической или химической обработки целлюлозы |
JP2008505869A JP5260276B2 (ja) | 2005-04-15 | 2006-04-07 | イオン性液体中のセルロース溶液 |
KR1020077023408A KR101376011B1 (ko) | 2005-04-15 | 2006-04-07 | 이온성 액체 중의 셀룰로오스 용액 |
US11/908,969 US7749318B2 (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
EP06847012.9A EP1881994B1 (de) | 2005-04-15 | 2006-04-07 | Lösungen von cellulose in ionischen flüssigkeiten |
CA2604557A CA2604557C (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
IL185441A IL185441A (en) | 2005-04-15 | 2007-08-22 | Cellulose solutions in ionic liquids |
NO20074302A NO20074302L (no) | 2005-04-15 | 2007-08-22 | Celluloselosninger i ioniske vaesker |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102005017715.8 | 2005-04-15 | ||
DE102005017715A DE102005017715A1 (de) | 2005-04-15 | 2005-04-15 | Lösungen von Cellulose in ionischen Flüssigkeiten |
Publications (2)
Publication Number | Publication Date |
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WO2007057235A2 true WO2007057235A2 (de) | 2007-05-24 |
WO2007057235A3 WO2007057235A3 (de) | 2007-12-13 |
Family
ID=37055478
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/061422 WO2007057235A2 (de) | 2005-04-15 | 2006-04-07 | Lösungen von cellulose in ionischen flüssigkeiten |
Country Status (15)
Country | Link |
---|---|
US (1) | US7749318B2 (de) |
EP (1) | EP1881994B1 (de) |
JP (1) | JP5260276B2 (de) |
KR (1) | KR101376011B1 (de) |
CN (1) | CN101160325B (de) |
AU (1) | AU2006314736B2 (de) |
BR (1) | BRPI0609083A2 (de) |
CA (1) | CA2604557C (de) |
DE (1) | DE102005017715A1 (de) |
EA (1) | EA016748B1 (de) |
IL (1) | IL185441A (de) |
NO (1) | NO20074302L (de) |
NZ (1) | NZ560914A (de) |
WO (1) | WO2007057235A2 (de) |
ZA (1) | ZA200708723B (de) |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4367191A (en) * | 1981-03-25 | 1983-01-04 | Research Corporation | Preparation of cellulose films or fibers from cellulose solutions |
US4750939A (en) * | 1986-12-02 | 1988-06-14 | North Carolina State University | Anisotropic cellulose solutions, fibers, and films formed therefrom |
EP0299824A1 (de) * | 1987-07-01 | 1989-01-18 | Institut Textile De France | Verfahren zur Herstellung einer Spinnlösung von Cellulose mit tertiärem Aminoxid und einem Zusatz |
WO2003029329A2 (en) * | 2001-10-03 | 2003-04-10 | The University Of Alabama | Dissolution and processing of cellulose using ionic liquids |
WO2006108861A2 (de) * | 2005-04-15 | 2006-10-19 | Basf Aktiengesellschaft | Löslichkeit von cellulose in ionischen flüssigkeiten unter zugabe von aminbase |
DE102005062608A1 (de) * | 2005-12-23 | 2007-07-05 | Basf Ag | Lösungssystem auf der Basis geschmolzener ionischer Flüssigkeiten ein Verfahren zu dessen Herstellung sowie zur Herstellung regenerierter Kohlenydrate |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1943176A (en) * | 1930-09-27 | 1934-01-09 | Chem Ind Basel | Cellulose solution |
US6808557B2 (en) * | 2001-10-03 | 2004-10-26 | The University Of Alabama | Cellulose matrix encapsulation and method |
MY138064A (en) * | 2002-01-24 | 2009-04-30 | Basf Ag | Method for the separation of acids from chemical reaction mixtures by means of ionic fluids |
DE10202838A1 (de) | 2002-01-24 | 2003-08-07 | Basf Ag | Verfahren zur Abtrennung von Säuren aus chemischen Reaktionsgemischen mit Hilfe von ionischen Flüssigkeiten |
JP4186063B2 (ja) * | 2003-09-19 | 2008-11-26 | 富士フイルム株式会社 | セルロース組成物、セルロースフィルム、およびセルロースフィルム用の改質剤 |
-
2005
- 2005-04-15 DE DE102005017715A patent/DE102005017715A1/de not_active Withdrawn
-
2006
- 2006-04-07 AU AU2006314736A patent/AU2006314736B2/en not_active Ceased
- 2006-04-07 BR BRPI0609083-4A patent/BRPI0609083A2/pt not_active IP Right Cessation
- 2006-04-07 EA EA200701783A patent/EA016748B1/ru not_active IP Right Cessation
- 2006-04-07 WO PCT/EP2006/061422 patent/WO2007057235A2/de active Application Filing
- 2006-04-07 EP EP06847012.9A patent/EP1881994B1/de not_active Not-in-force
- 2006-04-07 CA CA2604557A patent/CA2604557C/en not_active Expired - Fee Related
- 2006-04-07 KR KR1020077023408A patent/KR101376011B1/ko active IP Right Grant
- 2006-04-07 CN CN200680012598XA patent/CN101160325B/zh not_active Expired - Fee Related
- 2006-04-07 US US11/908,969 patent/US7749318B2/en not_active Expired - Fee Related
- 2006-04-07 NZ NZ560914A patent/NZ560914A/en not_active IP Right Cessation
- 2006-04-07 JP JP2008505869A patent/JP5260276B2/ja not_active Expired - Fee Related
-
2007
- 2007-08-22 IL IL185441A patent/IL185441A/en not_active IP Right Cessation
- 2007-08-22 NO NO20074302A patent/NO20074302L/no not_active Application Discontinuation
- 2007-10-12 ZA ZA200708723A patent/ZA200708723B/xx unknown
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4367191A (en) * | 1981-03-25 | 1983-01-04 | Research Corporation | Preparation of cellulose films or fibers from cellulose solutions |
US4750939A (en) * | 1986-12-02 | 1988-06-14 | North Carolina State University | Anisotropic cellulose solutions, fibers, and films formed therefrom |
EP0299824A1 (de) * | 1987-07-01 | 1989-01-18 | Institut Textile De France | Verfahren zur Herstellung einer Spinnlösung von Cellulose mit tertiärem Aminoxid und einem Zusatz |
WO2003029329A2 (en) * | 2001-10-03 | 2003-04-10 | The University Of Alabama | Dissolution and processing of cellulose using ionic liquids |
WO2006108861A2 (de) * | 2005-04-15 | 2006-10-19 | Basf Aktiengesellschaft | Löslichkeit von cellulose in ionischen flüssigkeiten unter zugabe von aminbase |
DE102005062608A1 (de) * | 2005-12-23 | 2007-07-05 | Basf Ag | Lösungssystem auf der Basis geschmolzener ionischer Flüssigkeiten ein Verfahren zu dessen Herstellung sowie zur Herstellung regenerierter Kohlenydrate |
Non-Patent Citations (1)
Title |
---|
DATABASE CA CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; XP002452139 gefunden im STN Database accession no. 142:338021 & DATABASE WPI Derwent Publications Ltd., London, GB; AN 2005-299127 & JP 2005 089689 A (FUJI PHOTO FILM CO LTD) 7. April 2005 (2005-04-07) & JP 2005 089689 A (FUJI PHOTO FILM CO LTD) 7. April 2005 (2005-04-07) * |
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DE102020125922B4 (de) | 2020-10-04 | 2022-06-02 | Elke Münch | Mobile Vorrichtung zur Reinigung und Desinfizierung von Raumluft |
DE102020125919B4 (de) | 2020-10-04 | 2022-06-23 | Elke Münch | Durch eine Temperaturdifferenz betreibbare, mobile Vorrichtung zur Reinigung und Desinfizierung von Raumluft und eine Testvorrichtung hierfür |
DE102020006226A1 (de) | 2020-10-10 | 2022-04-14 | LUCRAT GmbH | Mobile Vorichtung für die Reinigung und Desinfektion von Raumluft, Bausätze für ihren Zusammenbau und ihre Verwendung |
DE102020006226B4 (de) | 2020-10-10 | 2023-05-25 | LUCRAT GmbH | Mobile Vorichtung für die Reinigung und Desinfektion von Raumluft, Bausätze für ihren Zusammenbau und ihre Verwendung |
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EP1881994A2 (de) | 2008-01-30 |
CA2604557C (en) | 2016-06-21 |
NO20074302L (no) | 2008-01-09 |
US7749318B2 (en) | 2010-07-06 |
CN101160325A (zh) | 2008-04-09 |
AU2006314736B2 (en) | 2012-02-23 |
IL185441A (en) | 2013-04-30 |
AU2006314736A1 (en) | 2007-05-24 |
EA016748B1 (ru) | 2012-07-30 |
EA200701783A1 (ru) | 2008-04-28 |
US20080190321A1 (en) | 2008-08-14 |
NZ560914A (en) | 2011-02-25 |
DE102005017715A1 (de) | 2006-10-19 |
EP1881994B1 (de) | 2016-08-24 |
BRPI0609083A2 (pt) | 2010-11-16 |
WO2007057235A3 (de) | 2007-12-13 |
JP2008536972A (ja) | 2008-09-11 |
KR101376011B1 (ko) | 2014-03-19 |
CA2604557A1 (en) | 2007-05-24 |
ZA200708723B (en) | 2009-08-26 |
JP5260276B2 (ja) | 2013-08-14 |
IL185441A0 (en) | 2008-08-07 |
CN101160325B (zh) | 2012-04-04 |
KR20080006550A (ko) | 2008-01-16 |
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