DE102005017715A1 - Lösungen von Cellulose in ionischen Flüssigkeiten - Google Patents
Lösungen von Cellulose in ionischen Flüssigkeiten Download PDFInfo
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- DE102005017715A1 DE102005017715A1 DE102005017715A DE102005017715A DE102005017715A1 DE 102005017715 A1 DE102005017715 A1 DE 102005017715A1 DE 102005017715 A DE102005017715 A DE 102005017715A DE 102005017715 A DE102005017715 A DE 102005017715A DE 102005017715 A1 DE102005017715 A1 DE 102005017715A1
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- 150000001768 cations Chemical class 0.000 title claims abstract description 39
- 229920002678 cellulose Polymers 0.000 title claims abstract description 34
- 239000001913 cellulose Substances 0.000 title claims abstract description 34
- 229910052760 oxygen Inorganic materials 0.000 title claims abstract description 27
- 239000002608 ionic liquid Substances 0.000 title claims abstract description 26
- 239000001301 oxygen Substances 0.000 title claims abstract description 26
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title claims abstract description 25
- 150000001450 anions Chemical class 0.000 title claims abstract description 25
- 229910052757 nitrogen Inorganic materials 0.000 title claims abstract description 24
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 239000002904 solvent Substances 0.000 title claims abstract description 14
- 229910052717 sulfur Inorganic materials 0.000 title claims abstract description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title claims abstract description 9
- 239000011593 sulfur Substances 0.000 title claims abstract description 9
- 239000000126 substance Substances 0.000 title claims description 7
- 125000004437 phosphorous atom Chemical group 0.000 title description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000011574 phosphorus Substances 0.000 claims abstract description 5
- 238000002360 preparation method Methods 0.000 claims abstract description 3
- -1 oxonium cation Chemical class 0.000 claims description 464
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 83
- 229910052739 hydrogen Inorganic materials 0.000 claims description 63
- 239000001257 hydrogen Substances 0.000 claims description 63
- 125000003118 aryl group Chemical group 0.000 claims description 36
- 229910052736 halogen Inorganic materials 0.000 claims description 36
- 150000002367 halogens Chemical class 0.000 claims description 36
- 125000005842 heteroatom Chemical group 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 35
- 150000002431 hydrogen Chemical group 0.000 claims description 29
- 125000000524 functional group Chemical group 0.000 claims description 27
- 125000004104 aryloxy group Chemical group 0.000 claims description 26
- 125000003545 alkoxy group Chemical group 0.000 claims description 25
- 125000000623 heterocyclic group Chemical group 0.000 claims description 25
- 125000004434 sulfur atom Chemical group 0.000 claims description 17
- 229910004283 SiO 4 Inorganic materials 0.000 claims description 16
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 15
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 229910052751 metal Inorganic materials 0.000 claims description 12
- 239000002184 metal Substances 0.000 claims description 12
- 239000000460 chlorine Substances 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 10
- 229920006395 saturated elastomer Polymers 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- 150000001721 carbon Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 150000004820 halides Chemical class 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 4
- 125000002015 acyclic group Chemical group 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 235000021317 phosphate Nutrition 0.000 claims description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
- 239000005077 polysulfide Substances 0.000 claims description 4
- 229920001021 polysulfide Polymers 0.000 claims description 4
- 150000008117 polysulfides Polymers 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 3
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 3
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 3
- 150000003871 sulfonates Chemical class 0.000 claims description 3
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 3
- 150000003568 thioethers Chemical class 0.000 claims description 3
- 229910016467 AlCl 4 Inorganic materials 0.000 claims description 2
- 229910017008 AsF 6 Inorganic materials 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 229910021591 Copper(I) chloride Inorganic materials 0.000 claims description 2
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910018286 SbF 6 Inorganic materials 0.000 claims description 2
- 150000004703 alkoxides Chemical class 0.000 claims description 2
- 125000005621 boronate group Chemical class 0.000 claims description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 229910021645 metal ion Inorganic materials 0.000 claims description 2
- 125000005525 methide group Chemical group 0.000 claims description 2
- 125000005538 phosphinite group Chemical group 0.000 claims description 2
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 2
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical class O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 125000005463 sulfonylimide group Chemical group 0.000 claims description 2
- 150000007944 thiolates Chemical class 0.000 claims description 2
- 150000004651 carbonic acid esters Chemical class 0.000 claims 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 99
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 62
- 150000003254 radicals Chemical class 0.000 description 30
- 239000000243 solution Substances 0.000 description 22
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 21
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 14
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 9
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 9
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 8
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 8
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 8
- 150000002500 ions Chemical class 0.000 description 6
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 150000003512 tertiary amines Chemical class 0.000 description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 5
- 125000004093 cyano group Chemical group *C#N 0.000 description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 238000005956 quaternization reaction Methods 0.000 description 5
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000005588 protonation Effects 0.000 description 4
- 125000003944 tolyl group Chemical group 0.000 description 4
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 description 3
- STCBHSHARMAIOM-UHFFFAOYSA-N 1-methyl-1h-imidazol-1-ium;chloride Chemical compound Cl.CN1C=CN=C1 STCBHSHARMAIOM-UHFFFAOYSA-N 0.000 description 3
- KEQTWHPMSVAFDA-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole Chemical compound C1NNC=C1 KEQTWHPMSVAFDA-UHFFFAOYSA-N 0.000 description 3
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
- 125000004398 2-methyl-2-butyl group Chemical group CC(C)(CC)* 0.000 description 3
- 125000004918 2-methyl-2-pentyl group Chemical group CC(C)(CCC)* 0.000 description 3
- 125000004922 2-methyl-3-pentyl group Chemical group CC(C)C(CC)* 0.000 description 3
- 125000004917 3-methyl-2-butyl group Chemical group CC(C(C)*)C 0.000 description 3
- 125000004919 3-methyl-2-pentyl group Chemical group CC(C(C)*)CC 0.000 description 3
- 125000004921 3-methyl-3-pentyl group Chemical group CC(CC)(CC)* 0.000 description 3
- 125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 3
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 3
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 3
- LEHULSCLOPRJSL-UHFFFAOYSA-N n,n-dibutylpentan-1-amine Chemical compound CCCCCN(CCCC)CCCC LEHULSCLOPRJSL-UHFFFAOYSA-N 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 3
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 3
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- GNPSDJOWGWWXSS-UHFFFAOYSA-M 1-benzylpyridin-1-ium;chloride Chemical compound [Cl-].C=1C=CC=C[N+]=1CC1=CC=CC=C1 GNPSDJOWGWWXSS-UHFFFAOYSA-M 0.000 description 2
- MCTWTZJPVLRJOU-UHFFFAOYSA-O 1-methylimidazole Chemical compound CN1C=C[NH+]=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-O 0.000 description 2
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 2
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 description 2
- 125000003456 2,6-dinitrophenyl group Chemical group [H]C1=C([H])C(=C(*)C(=C1[H])[N+]([O-])=O)[N+]([O-])=O 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- 125000003006 2-dimethylaminoethyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 2
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 2
- 125000004042 4-aminobutyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])N([H])[H] 0.000 description 2
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 2
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 2
- SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 2
- UIOAQJNADLELPQ-UHFFFAOYSA-N C[C]1OCCO1 Chemical group C[C]1OCCO1 UIOAQJNADLELPQ-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002841 Lewis acid Substances 0.000 description 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000003857 carboxamides Chemical class 0.000 description 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 2
- 125000000068 chlorophenyl group Chemical group 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004188 dichlorophenyl group Chemical group 0.000 description 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
- 125000004212 difluorophenyl group Chemical group 0.000 description 2
- 125000005805 dimethoxy phenyl group Chemical group 0.000 description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
- ZZVUWRFHKOJYTH-UHFFFAOYSA-N diphenhydramine Chemical group C=1C=CC=CC=1C(OCCN(C)C)C1=CC=CC=C1 ZZVUWRFHKOJYTH-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000001041 indolyl group Chemical group 0.000 description 2
- 150000007517 lewis acids Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- KLVOSHOFGYMCCP-UHFFFAOYSA-N n,n-di(propan-2-yl)butan-1-amine Chemical compound CCCCN(C(C)C)C(C)C KLVOSHOFGYMCCP-UHFFFAOYSA-N 0.000 description 2
- HTDCNKTXDLRMHZ-UHFFFAOYSA-N n,n-dibutylcyclohexanamine Chemical compound CCCCN(CCCC)C1CCCCC1 HTDCNKTXDLRMHZ-UHFFFAOYSA-N 0.000 description 2
- UPNQFYMXRSHQBY-UHFFFAOYSA-N n,n-diethyl-2-methylpropan-2-amine Chemical compound CCN(CC)C(C)(C)C UPNQFYMXRSHQBY-UHFFFAOYSA-N 0.000 description 2
- 125000003518 norbornenyl group Chemical group C12(C=CC(CC1)C2)* 0.000 description 2
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical compound CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000004627 regenerated cellulose Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 2
- 125000005023 xylyl group Chemical group 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- FKTXDTWDCPTPHK-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical group FC(F)(F)[C](F)C(F)(F)F FKTXDTWDCPTPHK-UHFFFAOYSA-N 0.000 description 1
- RDTIFYBSPQERAS-UHFFFAOYSA-N 1,4,5-trimethylimidazole Chemical compound CC=1N=CN(C)C=1C RDTIFYBSPQERAS-UHFFFAOYSA-N 0.000 description 1
- MCMFEZDRQOJKMN-UHFFFAOYSA-N 1-butylimidazole Chemical compound CCCCN1C=CN=C1 MCMFEZDRQOJKMN-UHFFFAOYSA-N 0.000 description 1
- OSSNTDFYBPYIEC-UHFFFAOYSA-O 1-ethenylimidazole;hydron Chemical compound C=CN1C=C[NH+]=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-O 0.000 description 1
- IWDFHWZHHOSSGR-UHFFFAOYSA-N 1-ethylimidazole Chemical compound CCN1C=CN=C1 IWDFHWZHHOSSGR-UHFFFAOYSA-N 0.000 description 1
- KLMZKZJCMDOKFE-UHFFFAOYSA-N 1-octylimidazole Chemical compound CCCCCCCCN1C=CN=C1 KLMZKZJCMDOKFE-UHFFFAOYSA-N 0.000 description 1
- KXIXHISTUVHOCY-UHFFFAOYSA-N 1-propan-2-ylpiperidine Chemical compound CC(C)N1CCCCC1 KXIXHISTUVHOCY-UHFFFAOYSA-N 0.000 description 1
- RSVIUCBJPRWLIZ-UHFFFAOYSA-N 1-tert-butylpiperidine Chemical compound CC(C)(C)N1CCCCC1 RSVIUCBJPRWLIZ-UHFFFAOYSA-N 0.000 description 1
- WNMQSIGDRWCJMO-UHFFFAOYSA-N 1-tert-butylpyrrolidine Chemical compound CC(C)(C)N1CCCC1 WNMQSIGDRWCJMO-UHFFFAOYSA-N 0.000 description 1
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-O 2,3-dimethylimidazolium ion Chemical compound CC1=[NH+]C=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-O 0.000 description 1
- SZQCPPRPWDXLMM-UHFFFAOYSA-O 2,4-dimethyl-1h-pyrazol-2-ium Chemical compound C[NH+]1C=C(C)C=N1 SZQCPPRPWDXLMM-UHFFFAOYSA-O 0.000 description 1
- 125000001917 2,4-dinitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C(=C1*)[N+]([O-])=O)[N+]([O-])=O 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
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- DLMICMXXVVMDNV-UHFFFAOYSA-N n,n-di(propan-2-yl)propan-1-amine Chemical compound CCCN(C(C)C)C(C)C DLMICMXXVVMDNV-UHFFFAOYSA-N 0.000 description 1
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- BVUGARXRRGZONH-UHFFFAOYSA-N n,n-diethyloctan-1-amine Chemical compound CCCCCCCCN(CC)CC BVUGARXRRGZONH-UHFFFAOYSA-N 0.000 description 1
- YZULHOOBWDXEOT-UHFFFAOYSA-N n,n-diethylpentan-1-amine Chemical compound CCCCCN(CC)CC YZULHOOBWDXEOT-UHFFFAOYSA-N 0.000 description 1
- MMFBQHXDINNBMW-UHFFFAOYSA-N n,n-dipropylaniline Chemical compound CCCN(CCC)C1=CC=CC=C1 MMFBQHXDINNBMW-UHFFFAOYSA-N 0.000 description 1
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- MSHKXFDHUIFHMD-UHFFFAOYSA-N n-benzyl-n-butylbutan-1-amine Chemical compound CCCCN(CCCC)CC1=CC=CC=C1 MSHKXFDHUIFHMD-UHFFFAOYSA-N 0.000 description 1
- HSZCJVZRHXPCIA-UHFFFAOYSA-N n-benzyl-n-ethylaniline Chemical compound C=1C=CC=CC=1N(CC)CC1=CC=CC=C1 HSZCJVZRHXPCIA-UHFFFAOYSA-N 0.000 description 1
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- YLFDIUNVGXCCPV-UHFFFAOYSA-N n-benzyl-n-propylpropan-1-amine Chemical compound CCCN(CCC)CC1=CC=CC=C1 YLFDIUNVGXCCPV-UHFFFAOYSA-N 0.000 description 1
- BBDGYADAMYMJNO-UHFFFAOYSA-N n-butyl-n-ethylbutan-1-amine Chemical compound CCCCN(CC)CCCC BBDGYADAMYMJNO-UHFFFAOYSA-N 0.000 description 1
- VEBPYKMCKZTFPJ-UHFFFAOYSA-N n-butyl-n-propylbutan-1-amine Chemical compound CCCCN(CCC)CCCC VEBPYKMCKZTFPJ-UHFFFAOYSA-N 0.000 description 1
- 125000005246 nonafluorobutyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- SOWBFZRMHSNYGE-UHFFFAOYSA-N oxamic acid Chemical compound NC(=O)C(O)=O SOWBFZRMHSNYGE-UHFFFAOYSA-N 0.000 description 1
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- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
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- 238000001556 precipitation Methods 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical group CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
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- 125000001725 pyrenyl group Chemical group 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
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- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003511 tertiary amides Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
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- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 description 1
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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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
-
- 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
-
- 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
-
- 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]
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005017715A DE102005017715A1 (de) | 2005-04-15 | 2005-04-15 | Lösungen von Cellulose in ionischen Flüssigkeiten |
| CN200680012598XA CN101160325B (zh) | 2005-04-15 | 2006-04-07 | 离子液体中的纤维素溶液 |
| CA2604557A CA2604557C (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
| 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 |
| BRPI0609083-4A BRPI0609083A2 (pt) | 2005-04-15 | 2006-04-07 | solução, processo para preparar a mesma, e, uso de uma solução |
| US11/908,969 US7749318B2 (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
| AU2006314736A AU2006314736B2 (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids |
| KR1020077023408A KR101376011B1 (ko) | 2005-04-15 | 2006-04-07 | 이온성 액체 중의 셀룰로오스 용액 |
| EP06847012.9A EP1881994B1 (de) | 2005-04-15 | 2006-04-07 | Lösungen von cellulose in ionischen flüssigkeiten |
| JP2008505869A JP5260276B2 (ja) | 2005-04-15 | 2006-04-07 | イオン性液体中のセルロース溶液 |
| NZ560914A NZ560914A (en) | 2005-04-15 | 2006-04-07 | Cellulose solutions in ionic liquids based upon imidazolium cations |
| PCT/EP2006/061422 WO2007057235A2 (de) | 2005-04-15 | 2006-04-07 | Lösungen von cellulose in ionischen flüssigkeiten |
| 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 |
| ZA200708723A ZA200708723B (en) | 2005-04-15 | 2007-10-12 | Cellulose solutions in Ionic liquids |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005017715A DE102005017715A1 (de) | 2005-04-15 | 2005-04-15 | Lösungen von Cellulose in ionischen Flüssigkeiten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE102005017715A1 true DE102005017715A1 (de) | 2006-10-19 |
Family
ID=37055478
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE102005017715A Withdrawn DE102005017715A1 (de) | 2005-04-15 | 2005-04-15 | Lösungen von Cellulose in ionischen Flüssigkeiten |
Country Status (15)
| Country | Link |
|---|---|
| US (1) | US7749318B2 (enExample) |
| EP (1) | EP1881994B1 (enExample) |
| JP (1) | JP5260276B2 (enExample) |
| KR (1) | KR101376011B1 (enExample) |
| CN (1) | CN101160325B (enExample) |
| AU (1) | AU2006314736B2 (enExample) |
| BR (1) | BRPI0609083A2 (enExample) |
| CA (1) | CA2604557C (enExample) |
| DE (1) | DE102005017715A1 (enExample) |
| EA (1) | EA016748B1 (enExample) |
| IL (1) | IL185441A (enExample) |
| NO (1) | NO20074302L (enExample) |
| NZ (1) | NZ560914A (enExample) |
| WO (1) | WO2007057235A2 (enExample) |
| ZA (1) | ZA200708723B (enExample) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008098036A1 (en) * | 2007-02-06 | 2008-08-14 | North Carolina State University | Product preparation and recovery from thermolysis of lignocellulosics in ionic liquids |
| DE102009023458A1 (de) * | 2009-06-02 | 2010-12-30 | Carl Freudenberg Kg | Lösung, umfassend Cellulose, Verfahren zu deren Herstellung sowie deren Verwendung |
| US8182557B2 (en) | 2007-02-06 | 2012-05-22 | North Carolina State University | Use of lignocellulosics solvated in ionic liquids for production of biofuels |
| DE102011119840A1 (de) | 2010-12-01 | 2012-06-06 | Technische Universität Ilmenau | Polymerlösungen in ionischen Flüssigkeiten mit verbesserter thermischer und rheologischer Stabilität |
| DE102010061485A1 (de) | 2010-12-22 | 2012-06-28 | Chemetall Gmbh | Elektroden für Lithium-Batterien |
| US8435355B2 (en) | 2008-12-29 | 2013-05-07 | Weyerhaeuser Nr Company | Fractionation of lignocellulosic material using ionic liquids |
| DE102008029927B4 (de) * | 2008-06-26 | 2013-06-20 | Projektentwicklung Energie Und Umwelt Leipzig Gmbh | Flash-Pyrolyse von organischen Stoffen mit ionischer Flüssigkeit als Wärmeträger zur Herstellung von öligen bzw. gasförmigen Zwischenprodukten |
| US8486669B2 (en) | 2007-01-23 | 2013-07-16 | Basf Se | Enzymatic hydrolysis of a cellulose material treated with an ionic liquid |
| WO2014106650A2 (de) | 2013-01-03 | 2014-07-10 | EZER, Argun | Verfahren und vorrichtungen zur verölung von kohlenwasserstoffhaltigem eingangsmaterial |
| WO2014162062A1 (en) | 2013-04-04 | 2014-10-09 | Aalto University Foundation | Process for the production of shaped cellulose articles |
| WO2018138416A1 (en) | 2017-01-30 | 2018-08-02 | Aalto University Foundation Sr | A process for making a cellulose fibre or film |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US8044120B2 (en) | 2006-10-13 | 2011-10-25 | Basf Aktiengesellschaft | Ionic liquids for solubilizing polymers |
| EP2126104A1 (de) * | 2007-01-23 | 2009-12-02 | Basf Se | Verfahren zur herstellung von glucose durch enzymatische hydrolyse von cellulose, die unter verwendung einer ionischen flüssigkeit, welche ein polyatomiges anion besitzt, aus lignocellulosehaltigem material gewonnen wurde |
| US20080188636A1 (en) * | 2007-02-06 | 2008-08-07 | North Carolina State University | Polymer derivatives and composites from the dissolution of lignocellulosics in ionic liquids |
| US9834516B2 (en) * | 2007-02-14 | 2017-12-05 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
| US10174129B2 (en) | 2007-02-14 | 2019-01-08 | Eastman Chemical Company | Regioselectively substituted cellulose esters produced in a carboxylated ionic liquid process and products produced therefrom |
| US8153782B2 (en) * | 2007-02-14 | 2012-04-10 | Eastman Chemical Company | Reformation of ionic liquids |
| FR2912748B1 (fr) | 2007-02-16 | 2009-11-13 | Centre Nat Rech Scient | Alkyl h-phosphonates de n,n'-dialkylimidazouliums, d'ammoniums quaternaires et leurs utilisations |
| US7674608B2 (en) | 2007-02-23 | 2010-03-09 | The University Of Toledo | Saccharifying cellulose |
| AU2008226825B2 (en) | 2007-03-14 | 2013-02-21 | Suganit Systems, Inc. | Biomass pretreatment |
| BRPI0810874B1 (pt) | 2007-05-05 | 2017-06-13 | Basf Se | Ionic liquid, process for preparing a ionic liquid, and, using ionic liquids. |
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| CN103183832B (zh) * | 2011-12-28 | 2015-11-18 | 中国科学院青岛生物能源与过程研究所 | 一种磁性纤维素壳聚糖复合微球的制备方法 |
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| CN102838761B (zh) * | 2012-08-27 | 2014-05-07 | 中国热带农业科学院农产品加工研究所 | 一种防止纤维素在离子液体中降解的方法 |
| CN103833620A (zh) * | 2012-11-26 | 2014-06-04 | 海洋王照明科技股份有限公司 | 含硫类离子液体及其制备方法和应用 |
| US11118308B2 (en) | 2013-03-15 | 2021-09-14 | Ip2Ipo Innovations Limited | Treatment of lignocellulosic biomass with ionic liquid |
| JP2016527330A (ja) | 2013-05-24 | 2016-09-08 | メッツァ ファイバー オサケユキチュアＭｅｔｓａ Ｆｉｂｒｅ Ｏｙ | ポリマーを修飾する方法 |
| CN104610557B (zh) | 2013-11-01 | 2018-03-02 | 中国科学院化学研究所 | 一种再生纤维素膜、功能膜及其制备方法 |
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| CN105396561A (zh) * | 2015-12-12 | 2016-03-16 | 常州大学 | 一种综纤维素/壳聚糖微球吸附剂的制备方法 |
| CA3075264A1 (en) | 2017-09-08 | 2019-03-14 | Dte Materials Incorporated | Selectively depolymerizing cellulosic materials for use as thermal and acoustic insulators |
| GB2583719B (en) | 2019-05-02 | 2023-05-31 | Worn Again Tech Ltd | Recycling process |
| CN111945455A (zh) * | 2020-07-29 | 2020-11-17 | 中北大学 | 一种谷糠纤维素的提取方法及谷糠纤维膜的制备方法 |
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| DE102020125921B4 (de) | 2020-10-04 | 2022-05-19 | Elke Münch | Durch eine Temperaturdifferenz betreibbare, mobile Vorrichtung zur Reinigung und Desinfizierung von Raumluft |
| EP3978038A1 (de) | 2020-10-04 | 2022-04-06 | Elke Münch | Durch eine temperaturdifferenz betreibbare, mobile vorrichtung zur reinigung und desinfizierung von raumluft und eine testvorrichtung hierfür |
| EP3981442A1 (de) | 2020-10-04 | 2022-04-13 | Elke Münch | Durch eine temperaturdifferenz betreibbare, mobile vorrichtung zur reinigung und desinfizierung von raumluft |
| 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 |
| DE102024102529B3 (de) | 2024-01-30 | 2025-01-09 | Elke Münch | Vorrichtung und Verfahren für die reversible Adsorption und Desorption des Kohlendioxids in Verbrennungsabgasen |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1943176A (en) | 1930-09-27 | 1934-01-09 | Chem Ind Basel | Cellulose solution |
| 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 |
| FR2617511B1 (fr) | 1987-07-01 | 1989-12-15 | Inst Textile De France | Procede de preparation d'une solution de filage de cellulose en presence d'oxyde d'amine tertiaire et d'additif |
| US6824599B2 (en) * | 2001-10-03 | 2004-11-30 | The University Of Alabama | Dissolution and processing of cellulose using ionic liquids |
| 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 |
| DE102005017733A1 (de) * | 2005-04-15 | 2006-10-19 | Basf Ag | 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 |
-
2005
- 2005-04-15 DE DE102005017715A patent/DE102005017715A1/de not_active Withdrawn
-
2006
- 2006-04-07 BR BRPI0609083-4A patent/BRPI0609083A2/pt not_active IP Right Cessation
- 2006-04-07 AU AU2006314736A patent/AU2006314736B2/en not_active Ceased
- 2006-04-07 WO PCT/EP2006/061422 patent/WO2007057235A2/de not_active Ceased
- 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
- 2006-04-07 KR KR1020077023408A patent/KR101376011B1/ko not_active Expired - Fee Related
- 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 CN CN200680012598XA patent/CN101160325B/zh not_active Expired - Fee Related
- 2006-04-07 EA EA200701783A patent/EA016748B1/ru not_active IP Right Cessation
- 2006-04-07 US US11/908,969 patent/US7749318B2/en not_active Expired - Fee Related
-
2007
- 2007-08-22 NO NO20074302A patent/NO20074302L/no not_active Application Discontinuation
- 2007-08-22 IL IL185441A patent/IL185441A/en not_active IP Right Cessation
- 2007-10-12 ZA ZA200708723A patent/ZA200708723B/xx unknown
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8486669B2 (en) | 2007-01-23 | 2013-07-16 | Basf Se | Enzymatic hydrolysis of a cellulose material treated with an ionic liquid |
| WO2008098036A1 (en) * | 2007-02-06 | 2008-08-14 | North Carolina State University | Product preparation and recovery from thermolysis of lignocellulosics in ionic liquids |
| US7959765B2 (en) | 2007-02-06 | 2011-06-14 | North Carolina State Universtiy | Product preparation and recovery from thermolysis of lignocellulosics in ionic liquids |
| US8182557B2 (en) | 2007-02-06 | 2012-05-22 | North Carolina State University | Use of lignocellulosics solvated in ionic liquids for production of biofuels |
| DE102008029927B4 (de) * | 2008-06-26 | 2013-06-20 | Projektentwicklung Energie Und Umwelt Leipzig Gmbh | Flash-Pyrolyse von organischen Stoffen mit ionischer Flüssigkeit als Wärmeträger zur Herstellung von öligen bzw. gasförmigen Zwischenprodukten |
| US8435355B2 (en) | 2008-12-29 | 2013-05-07 | Weyerhaeuser Nr Company | Fractionation of lignocellulosic material using ionic liquids |
| DE102009023458A1 (de) * | 2009-06-02 | 2010-12-30 | Carl Freudenberg Kg | Lösung, umfassend Cellulose, Verfahren zu deren Herstellung sowie deren Verwendung |
| EP2460843A1 (de) | 2010-12-01 | 2012-06-06 | Thüringisches Institut für Textil- Und Kunststoff- Forschung E.V. | Polymerlösungen in ionischen Flüssigkeiten mit verbesserter thermischer und rheologischer Stabilität |
| DE102011119840A1 (de) | 2010-12-01 | 2012-06-06 | Technische Universität Ilmenau | Polymerlösungen in ionischen Flüssigkeiten mit verbesserter thermischer und rheologischer Stabilität |
| DE102010061485A1 (de) | 2010-12-22 | 2012-06-28 | Chemetall Gmbh | Elektroden für Lithium-Batterien |
| WO2012084878A1 (de) | 2010-12-22 | 2012-06-28 | Chemetall Gmbh | Elektroden für lithium-batterien |
| WO2014106650A2 (de) | 2013-01-03 | 2014-07-10 | EZER, Argun | Verfahren und vorrichtungen zur verölung von kohlenwasserstoffhaltigem eingangsmaterial |
| WO2014162062A1 (en) | 2013-04-04 | 2014-10-09 | Aalto University Foundation | Process for the production of shaped cellulose articles |
| WO2018138416A1 (en) | 2017-01-30 | 2018-08-02 | Aalto University Foundation Sr | A process for making a cellulose fibre or film |
| US11549200B2 (en) | 2017-01-30 | 2023-01-10 | Aalto University Foundation Sr | Process for making cellulose fibre or film |
Also Published As
| Publication number | Publication date |
|---|---|
| IL185441A0 (en) | 2008-08-07 |
| WO2007057235A2 (de) | 2007-05-24 |
| EP1881994B1 (de) | 2016-08-24 |
| CA2604557A1 (en) | 2007-05-24 |
| CN101160325B (zh) | 2012-04-04 |
| AU2006314736A1 (en) | 2007-05-24 |
| CN101160325A (zh) | 2008-04-09 |
| AU2006314736B2 (en) | 2012-02-23 |
| EP1881994A2 (de) | 2008-01-30 |
| IL185441A (en) | 2013-04-30 |
| JP5260276B2 (ja) | 2013-08-14 |
| EA016748B1 (ru) | 2012-07-30 |
| WO2007057235A3 (de) | 2007-12-13 |
| ZA200708723B (en) | 2009-08-26 |
| CA2604557C (en) | 2016-06-21 |
| BRPI0609083A2 (pt) | 2010-11-16 |
| NO20074302L (no) | 2008-01-09 |
| US20080190321A1 (en) | 2008-08-14 |
| NZ560914A (en) | 2011-02-25 |
| KR20080006550A (ko) | 2008-01-16 |
| KR101376011B1 (ko) | 2014-03-19 |
| US7749318B2 (en) | 2010-07-06 |
| JP2008536972A (ja) | 2008-09-11 |
| EA200701783A1 (ru) | 2008-04-28 |
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