WO2015086125A1 - Reinigungsvorrichtung - Google Patents
Reinigungsvorrichtung Download PDFInfo
- Publication number
- WO2015086125A1 WO2015086125A1 PCT/EP2014/003207 EP2014003207W WO2015086125A1 WO 2015086125 A1 WO2015086125 A1 WO 2015086125A1 EP 2014003207 W EP2014003207 W EP 2014003207W WO 2015086125 A1 WO2015086125 A1 WO 2015086125A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cleaning device
- flow chamber
- flow
- liquid crystal
- mixture
- Prior art date
Links
- 238000004140 cleaning Methods 0.000 title claims abstract description 76
- 239000000203 mixture Substances 0.000 claims abstract description 136
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 79
- 239000002594 sorbent Substances 0.000 claims abstract description 34
- 239000004033 plastic Substances 0.000 claims abstract description 14
- 229920003023 plastic Polymers 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 9
- 239000002184 metal Substances 0.000 claims abstract description 9
- 239000011248 coating agent Substances 0.000 claims abstract description 7
- 238000000576 coating method Methods 0.000 claims abstract description 7
- 238000001816 cooling Methods 0.000 claims abstract description 4
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 239000002131 composite material Substances 0.000 claims abstract description 3
- 238000009826 distribution Methods 0.000 claims description 34
- 238000000746 purification Methods 0.000 claims description 25
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical class O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000000741 silica gel Substances 0.000 claims description 18
- 229910002027 silica gel Inorganic materials 0.000 claims description 18
- 239000010457 zeolite Substances 0.000 claims description 16
- 239000012459 cleaning agent Substances 0.000 claims description 5
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000391 magnesium silicate Substances 0.000 claims description 5
- 229910052919 magnesium silicate Inorganic materials 0.000 claims description 5
- 235000019792 magnesium silicate Nutrition 0.000 claims description 5
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 4
- 229910021536 Zeolite Inorganic materials 0.000 claims 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
- 238000013461 design Methods 0.000 abstract description 4
- 239000002245 particle Substances 0.000 description 36
- 150000001875 compounds Chemical class 0.000 description 30
- 238000000034 method Methods 0.000 description 24
- 239000000126 substance Substances 0.000 description 20
- 230000008569 process Effects 0.000 description 17
- 239000011148 porous material Substances 0.000 description 16
- 238000002156 mixing Methods 0.000 description 15
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 14
- 238000001179 sorption measurement Methods 0.000 description 12
- 239000012071 phase Substances 0.000 description 11
- -1 polytetrafluoroethylene Polymers 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 229910052731 fluorine Inorganic materials 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- 239000002019 doping agent Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 125000006850 spacer group Chemical group 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 239000003999 initiator Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 238000011049 filling Methods 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 0 C*c(c(F)cc(-c(c(F)c1)ccc1C(C=C1)=CCC1=C1CCC(C)CC1)c1)c1F Chemical compound C*c(c(F)cc(-c(c(F)c1)ccc1C(C=C1)=CCC1=C1CCC(C)CC1)c1)c1F 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 125000001072 heteroaryl group Chemical group 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000005485 electric heating Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 230000002452 interceptive effect Effects 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229910052714 tellurium Inorganic materials 0.000 description 2
- 238000009827 uniform distribution Methods 0.000 description 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 1
- HNEGJTWNOOWEMH-UHFFFAOYSA-N 1-fluoropropane Chemical group [CH2]CCF HNEGJTWNOOWEMH-UHFFFAOYSA-N 0.000 description 1
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000006043 5-hexenyl group Chemical group 0.000 description 1
- HVTJQICZTQZLSK-UHFFFAOYSA-N CC(C(Oc(cc1)ccc1-c(cc1)ccc1OC(C(C)=C)=O)=O)=C Chemical compound CC(C(Oc(cc1)ccc1-c(cc1)ccc1OC(C(C)=C)=O)=O)=C HVTJQICZTQZLSK-UHFFFAOYSA-N 0.000 description 1
- KBZQJAMUYAMVEK-UHFFFAOYSA-N CC(CC1)CCC1C1CCCCC1 Chemical compound CC(CC1)CCC1C1CCCCC1 KBZQJAMUYAMVEK-UHFFFAOYSA-N 0.000 description 1
- KSMVBYPXNKCPAJ-UHFFFAOYSA-N CC(CC1)CCC1N Chemical compound CC(CC1)CCC1N KSMVBYPXNKCPAJ-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 229940123457 Free radical scavenger Drugs 0.000 description 1
- 101000610640 Homo sapiens U4/U6 small nuclear ribonucleoprotein Prp3 Proteins 0.000 description 1
- 101001110823 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L6-A Proteins 0.000 description 1
- 101000712176 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L6-B Proteins 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 102100040374 U4/U6 small nuclear ribonucleoprotein Prp3 Human genes 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- RBBNOVKRLWDEGC-UHFFFAOYSA-M dodecyl-ethyl-dimethylazanium;4-hexoxybenzoate Chemical compound CCCCCCOC1=CC=C(C([O-])=O)C=C1.CCCCCCCCCCCC[N+](C)(C)CC RBBNOVKRLWDEGC-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000013536 elastomeric material Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 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 1
- 125000005549 heteroarylene group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
- B01D15/22—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the construction of the column
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- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
- B01D15/14—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the introduction of the feed to the apparatus
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
- B01D15/20—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to the conditioning of the sorbent material
- B01D15/206—Packing or coating
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3066—Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3402—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/542—Macromolecular compounds
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2201/00—Details relating to filtering apparatus
- B01D2201/30—Filter housing constructions
- B01D2201/301—Details of removable closures, lids, caps, filter heads
- B01D2201/302—Details of removable closures, lids, caps, filter heads having inlet or outlet ports
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2201/00—Details relating to filtering apparatus
- B01D2201/30—Filter housing constructions
- B01D2201/301—Details of removable closures, lids, caps, filter heads
- B01D2201/304—Seals or gaskets
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2201/00—Details relating to filtering apparatus
- B01D2201/34—Seals or gaskets for filtering elements
- B01D2201/347—Radial sealings
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
- C09K2019/0448—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
- C09K2019/0466—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the linking chain being a -CF2O- chain
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3004—Cy-Cy
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
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- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3009—Cy-Ph
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/301—Cy-Cy-Ph
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3016—Cy-Ph-Ph
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
- C09K19/3001—Cyclohexane rings
- C09K19/3003—Compounds containing at least two rings in which the different rings are directly linked (covalent bond)
- C09K2019/3027—Compounds comprising 1,4-cyclohexylene and 2,3-difluoro-1,4-phenylene
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3402—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom
- C09K2019/3422—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom the heterocyclic ring being a six-membered ring
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09K19/00—Liquid crystal materials
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their chemical composition
- C09K19/542—Macromolecular compounds
- C09K2019/548—Macromolecular compounds stabilizing the alignment; Polymer stabilized alignment
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- C09K2219/00—Aspects relating to the form of the liquid crystal [LC] material, or by the technical area in which LC material are used
Definitions
- the invention describes a cleaning device, in particular for the purification of a liquid-crystal mixture, and the use thereof.
- Liquid crystal mixtures are usually produced in mixing devices in which
- Sorbent is added, with the help of the cleaning process is performed.
- the amount of sorbent is dependent, among other things, on the liquid crystal mixture amount and the type of mixture.
- the sorbent is introduced into the mixing device and by means of a
- Heat is mixed with the liquid-crystal mixture to be purified. Subsequently, the suspension thus provided is filtered using a filter unit, e.g. a plate filter is filtered so that the sorbent is separated with the adhering or absorbed therein components of the liquid crystal mixture.
- a filter unit e.g. a plate filter is filtered so that the sorbent is separated with the adhering or absorbed therein components of the liquid crystal mixture.
- the object of the invention is to provide a cleaning device for the purification of liquid-crystal mixtures, which achieves an efficient purification of the liquid-crystal mixture in a structurally simple manner.
- the cleaning of the liquid-crystal mixture should be able to be carried out as quickly and effectively as possible.
- the cleaning process should, if possible with little design effort in mixing or
- CONFIRMATION COPY Filling processes can be integrated, which are necessary for the production of the
- a cleaning device for the purification of a liquid-crystal mixture having a flow-through chamber, which has an inlet opening and an outlet opening arranged opposite the inlet opening, around which
- Inlet opening is arranged, and with at least one filter element, which is arranged in the region of the outlet opening, wherein a measured in the flow direction length of the flow chamber is at least a factor of 1 greater than a maximum Lichtes measure of the flow chamber transverse to the flow direction.
- the length is at least a factor of 2 and more advantageously at least a factor of 3 to 34 greater than the largest light measure.
- the cleaning device according to the invention is used for the purification of liquid-crystal mixtures.
- the liquid-crystal mixture is introduced through the inlet opening into the flow chamber and with the aid of the flow distribution element arranged in the region of the inlet opening as uniformly as possible over the entire length
- Flow distribution element is preferably designed pore-shaped, wherein by means of the pores, a uniform distribution of the incoming liquid crystal mixture in the flow through the
- the flow distribution element can also be designed as a fabric.
- a detergent, or a sorbent is suitably arranged, which is flowed through or flowed around by the liquid crystal mixture.
- Liquid crystal mixture with the detergent, or the sorbent can during the flow through the flow chamber a very effective cleaning or separation of the components to be removed from the liquid-crystal mixture take place.
- the filter element which covers the outlet opening and the liquid crystal mixture in the
- the cleaning agent or the sorbent as well as components adhering to or absorbed therein as well as larger particles are retained, so that only the purified liquid-crystal mixture can leave the flow chamber.
- a liquid crystal mixture for example, immediately before filling a storage or
- Transport container can be cleaned with sufficient quality.
- a sorbent is preferably arranged in the flow chamber.
- the sorbent may also be referred to as sorbent within the meaning of the invention. Sorption is a collective term for various
- Enrichment processes and includes adsorption and absorption. During adsorption, a substance is deposited on an interface between two phases, whereas an absorption results in a
- the sorbent fills an interior in the flow chamber at least 50%.
- the amount of sorbent may vary depending on the amount of the Liquid crystal mixture and of any product requirements (for example, purity) are given.
- sorbents known to those skilled in the art are suitable for purification.
- alumina silica gel
- modified silica gel e.g. RP2, RP4, RP8 and RP18
- Magnesium silicate or zeolites with different modules are preferred. It is also possible to use mixtures of different sorbents. This can also be a sorbent with two
- pore and / or grain sizes Preferably, only one sorbent or a mixture of two sorbents is used.
- the mixture of two sorbents can be mixed with each other in any ratio. It is often advisable to carry out the purification first with a silica gel or aluminum oxide, followed by a further purification with zeolites.
- the grain size of the sorbents and the pore sizes may vary depending on the liquid-crystal mixture to be purified, with a broad spectrum
- Grain sizes in the column according to the invention is usable. Suitable particle sizes are, for example, 60-500 ⁇ m, but also 30-63 ⁇ m.
- Preferred sorbents have pore sizes of 4-30 nm, in particular 4-15 nm.
- the specific surface areas for the sorbents are generally from 30 to 1000 m 2 / g.
- sorbents are mentioned below: aluminum oxides and zeolites, for example from Merck KGaA, molecular sieve, silica gel, for example from Grace,
- the preferred sorbents can also be modified in their surface condition or, for example, be provided with specific chemical or biological capture molecules.
- Liquid crystal mixture is significantly improved, as a higher
- Cleaning device according to the invention can be significantly reduced.
- Water content of the mixture can be significantly further reduced, which also leads to a significant improvement of fina) s product.
- the flow chamber is preferably at least sectionally column-shaped and the light dimension of the flow chamber corresponds to a diameter in this section.
- a columnar design of the cleaning device facilitates the arrangement of the cleaning device on a further container, which is needed for the production or filling of the liquid crystal mixture, or is used. So the cleaning device can directly to the
- Components (polar compounds, solvents, etc.) can be achieved at the highest possible flow rate. As a result, the process times for the purification can be reduced, which in turn allows low production costs.
- At least one flow distribution element and at least one filter element are arranged in the flow chamber in the region of the inlet opening and in the region of the outlet opening.
- the flow chamber can be flowed through without modifications from both sides, or the inlet opening can optionally also be used as an outlet opening and the outlet opening as an inlet opening. This will increase the scope of the
- the cleaning device has a low weight and is portable.
- the cleaning device can be easily and quickly attached to a container, such as a mixing device or to a storage container, be connected to the reception of the cleaned
- Liquid crystal mixture is provided.
- connection means which, in particular, can be used as quick connection means (for example as a quick connection means)
- Allow connection with a container such as a subsequent mixing device or a reservoir.
- the flow chamber, or column and their components are preferably made of stainless steel.
- Stainless steel is resistant to water, water vapor, humidity and weak
- alloyed or unalloyed steels zirconium, titanium, glass, enamel or plastics.
- an adhesion-reducing inner coating is applied on inner surfaces of the flow chamber.
- the inner surfaces that is, the product facing surfaces within the flow chamber, an adhesion-reducing inner coating.
- plastics preferably polymers, particularly preferably polytetrafluoroethylene can be used as a coating.
- a continuous flow of the liquid crystal mixture is supported.
- test series have shown that, when using a suitable coating material, neither the inner surfaces of the flow Chamber even by the coating itself, the product quality of the purified liquid crystal mixture can be affected.
- the flow chamber preferably has giattwandige inside surfaces, which have a roughness of significantly less than 0.3 pm. This can be a sticking of the sorbent material, but also the liquid crystal mixture can be avoided on the inner surfaces, whereby the flow of liquid through the chamber,
- Giattwandige inside surfaces can be achieved in particular by grinding, passivation and pickling, as well as electropolishing of stainless steels.
- the cleaning device and in particular the flow chamber can be used with conventional temperature control devices, for example with a thermostatisable jacket, in particular with an outer double jacket, with outside on the flow chamber adjacent pipes or with welded
- Electric heating sleeves can also be used for heat input.
- Cooling media can be liquid or gaseous. Also possible is any execution of an electric heating on an outer wall of the
- Liquid crystal mixture can be significantly improved after a single cleaning step.
- the at least one flow distribution element is advantageously releasably secured to the flow chamber by means of a connection means.
- the connecting means may in particular be a clamping connection or a flange connection.
- Cleaning device at least one seal, which seals the at least one flow distribution element to the flow chamber out.
- seals which are preferably arranged both in the region of the inlet opening and in the region of the outlet opening can
- materials such as polytetrafluoroethylene proved to be suitable, which are designed for example as O-ring, C-ring or cone shape. Plate seals or jacketed O-ring seals can also be used as seals. Further, extruded seals with radially projecting sealing lips or gaskets of a perfluorinated elastomeric material may be advantageous. Also to be mentioned is the so-called “piston principle", wherein the volume of the column can be adjusted according to the batch volume with the aid of a movable piston.
- the flow distribution element is advantageously provided with a
- the fitting is preferably centered on the flow distribution element and in the case of a columnar
- the flow distribution element and the connection piece are made of one part.
- the flow distribution element and the connecting piece are preferably made of metal, in particular stainless steel or plastic.
- connection piece is connected with a quick connection means, in particular with a clamp connection, directly to a container which is used immediately preceding or following in the process chain of the production process.
- Connecting means is advantageously universally applicable and can be connected to differently designed containers, so that it can be connected, for example, to differently configured mixing devices or reservoirs if necessary.
- the liquid crystal mixture can be introduced via the connection piece directly into the flow chamber, so that a high
- Process speed that is, a short production time is achieved because no separate purification and filtering step is necessary.
- the connector can be preceded by an additional filter element.
- foreign bodies or clumps can be filtered by an additional filter unit in the region of the inlet opening of the flow chamber.
- Preferred filter elements are made of plastic or metal, wherein embodiments of sintered metal, plastic fabric and metal fabric are advantageous.
- Cross section of the flow chamber takes place. Furthermore, it can be ensured by the use of a filter element in the region of the outlet opening of the flow chamber that no sorbent remains in the purified liquid crystal mixture and thus to later
- a plurality of differently configured filter elements can be used and arranged with different pore sizes in the cleaning device.
- the cleaning device can advantageously be covered with a covering means, in particular a detachably connectable lid, wherein the lid is connected to the flow chamber with a clamping connection or flange connection.
- a covering means in particular a detachably connectable lid, wherein the lid is connected to the flow chamber with a clamping connection or flange connection.
- the cover also has a preferably centrally disposed opening for the
- the covering may be made of metal or plastic, for example.
- the covering means has a connection means, in particular a quick connection means, with which it can be connected to the flow chamber or to the cleaning device.
- a connection means in particular a quick connection means, with which it can be connected to the flow chamber or to the cleaning device.
- the quick connection means and the cleaning device can be connected to a container.
- a preferred fast connection means is, for example, a standardized clamp connection, which can also be referred to as a clamp connection.
- Figure 1 shows a cleaning device 1, which has a flow chamber 2 with a columnar interior.
- Flow chamber 2 is a sorbent (not shown)
- the liquid crystal mixture which performs the sorption of the substances to be removed from the liquid crystal mixture, such as polar compounds, particles, water, solvents, etc.
- the liquid crystal mixture can have one in the picture above
- inlet opening 3 are introduced into the flow chamber 2 and via an inlet opening arranged opposite the outlet opening 4 again flow out of the flow chamber 2, or flow out.
- Flow distribution element 5 is arranged, which at a
- Flow chamber 2 distributed so that a maximum effective contact time of the flowing liquid crystal mixture is achieved with the sorbent, or with the surface-active sorbent.
- annular seal 9 is provided in the region of the inlet opening 3.
- the seal 9 is located on the Flow distribution element 5 at.
- the connection between the seal 9 and the flow distribution element 5 is by a
- Connecting means 8 ensures that in the present
- Embodiment is a clamp connection.
- the flow distribution element 5 is designed such that it covers at least 50%, or more than 75% of the surface of the filter element 6 in the illustrated embodiment. This ensures that the liquid crystal mixture before entering the
- Flow chamber 2 distributed and pre-filtered at the same time. As a result, the sorption process can be significantly improved and the reaction time can be shortened.
- the flow direction extends from the top of the inlet opening 3 to the downwardly disposed outlet opening 4.
- the flow chamber 2 has a length in the flow direction, which is about a factor of 2 larger than the diameter and thus as a maximum light measure the
- Flow chamber 2 is transverse to the flow direction. It has surprisingly been found that for certain liquid-crystal mixtures by such a ratio of length to diameter, a short reaction time and a sufficiently good purification quality are achieved, which is reflected in an improved efficiency.
- Filter element 6 is arranged. Another flow distribution element 5 ensures in front of the outlet opening 4 that the through the first
- Liquid crystal mixture are introduced into a container, not shown, which can be connected by means of a suitable connection means 11 (for example, a clamping connection) with the cleaning device 1.
- the connector 10 has a releasably secured to the connector 10 cover 12 (in the present embodiment, a cover cap).
- the cover 12 is by means of another
- the cleaning device 1 is configured symmetrically, that is to say that the inlet opening 3 and the outlet opening 4 are also interchanged and the throughflow direction provided for a cleaning process
- Filter element 6 is arranged. At both openings 3 and 4, a connecting piece 0 is in each case arranged, which with a cover 12th
- This embodiment of the cleaning device 1 is particularly advantageous because a simple and reliable installation of the cleaning device 1 within a
- Production plant for liquid crystal mixtures allows and can be done with the cleaning device 1 a quick purification and subsequent filling of the liquid crystal mixture.
- liquid-crystal mixtures containing at least two organic substances, preferably mesogenic, in particular liquid-crystalline substances, are purified with the device according to the invention, the organic substances preferably being selected from the compounds of general formula I,
- -CH CH-, -CF 2 O-, -OCF 2 -, -OC-O- or -O-CO- may be replaced so that O atoms are not directly linked to one another, and one of the radicals R 1 , R 2 also is F, Cl, CN, SF 5, NCS, SCN, OCN
- Rings A, B, C, D, E are each independently
- r, s and t are each independently 0, 1, 2 or 3, where r + s + t
- Z "4 are each independently of one another -CO-O-, -O-CO-, -CF 2 O-,
- L 1 and L 2 are each independently H or F, mean.
- Z and Z 4 are preferably selected such that, if they do not represent a single bond, they are not linked together by two O atoms.
- the liquid-crystal mixtures to be purified from the mesogenic individual substances of the formula I may additionally also contain one or more polymerisable compounds, so-called reactive mesogens (RMs), for example, as disclosed in US Pat. No. 6,861,007, in concentrations of preferably 0.12-5% by weight, particularly preferably 0.2-2%, based on the mixture.
- RMs reactive mesogens
- Such mixtures can be used for so-called polymer-stabilized VA (PS-VA) modes, negative IPS (PS-IPS) or negative FFS (PS-FFS) modes in which a polymerization of the reactive mesogens in the liquid-crystalline mixture is to take place become.
- liquid-crystal mixture itself contains no polymerizable individual substances which also polymerize under the conditions where the reactive mesogens react.
- the polymerisable mesogenic or liquid-crystalline compounds also referred to as “reactive mesogens” (RM) are preferably selected from the compounds of the formula II,
- a 1 and A 2 are each independently an aromatic
- heteroaromatic, alicyclic or heterocyclic group preferably having 4 to 25 C atoms, which may also contain annelated rings, and which is optionally monosubstituted or polysubstituted by L,
- Z 1 is the same or different at each occurrence -O-, -S-, -CO-,
- L, R a and R are each independently H, halogen, SF 5 , NO 2 , a
- Carbon group or hydrocarbon group the compounds containing at least one radical L, R a and R b , which contains or contains a group P-Sp-,
- R ° and R 00 are each, independently of one another, H or alkyl having 1 to 12 C atoms, P is a polymerizable group,
- Sp is a spacer group or a single bond
- n 0, 1, 2, 3 or 4.
- the polymerizable compounds may have one polymerizable group (monoreactive) or two or more (di- or multi-reactive), preferably two polymerizable groups.
- meogenic group is known to those skilled in the art and described in the literature, and means a group that contributes significantly by the anisotropy of their attractive and repulsive interactions, in low molecular weight or polymeric substances
- mesogenic compounds may not necessarily have an FK phase themselves. It is also possible that mesogenic compounds show FK phase behavior only after mixing with other compounds and / or after polymerization.
- Typical mesogenic groups are, for example, rigid rod-shaped or disc-shaped units.
- spacer group (Engl. "Spacer” or “spacer group”), also referred to below as “Sp”, is known to the person skilled in the art and described in the literature, see, for example, Pure Appl. Chem. 73 (5), 888 (2001) and C. Tschierske, G. Pelzl, S. Diele, Angew. Chem. 2004, 116, 6340-6368. Unless otherwise indicated, the term indicates
- a group comprising, in a polymerizable mesogenic compound ("RM"), the mesogenic group and the polymerizable group (s) together combines.
- RM polymerizable mesogenic compound
- Sp is a single bond or a C 1-6 alkylene, wherein one or more CH 2 groups can be replaced by -O-, -CO-, -COO- or -OCO- so that not two O atoms directly connected to each other.
- organic group means a carbon or
- Hydrocarbon group means a carbon group which additionally has one or more H atoms and optionally one or more
- Heteroatoms such as N, O, S, P, Si, Se, As, Te or Ge contains.
- Halogen means F, Cl, Br or I.
- alkyl also include polyvalent groups, for example alkylene, arylene, heteroarylene, etc.
- alkyl in this application encompasses straight-chain and branched alkyl groups having 1-7 carbon atoms, in particular the straight-chain groups methyl, ethyl, propyl, butyl, pentyl, hexyl and heptyl. Groups of 1-6 carbon atoms are generally preferred.
- alkenyl in this application encompasses straight-chain and branched alkenyl groups having 2-7 carbon atoms, in particular the straight-chain groups.
- Preferred alkenyl groups are C 2 -C 7 -11 -alkenyl, C 4 -C 7 -E-alkenyl, C 5 -C 7 -alkenyl, C 6 -C 7 -5-alkenyl and C 7 -6-alkenyl, in particular C 2 -C 7 -1E-alkenyl, C 4 -C 7 -EE-alkenyl and C 5 -C 7 -alkenyl.
- alkenyl groups are vinyl, E-propenyl, E-butenyl, 1E-pentenyl, 1E-hexenyl, 1E-heptenyl, 3-butenyl, 3E-pentenyl, 3E-hexenyl, 3E-heptenyl, 4-pentenyl, 4Z-hexenyl, 4E-hexenyl, 4Z-heptenyl, 5-hexenyl, 6-heptenyl and the like. Groups of up to 5 carbon atoms are generally preferred.
- fluoroalkyl in this application includes straight-chain groups having at least one fluorine atom, preferably one
- fluorine i. Fluoromethyl, 2-fluoroethyl, 3-fluoropropyl, 4-fluorobutyl, 5-fluoropentyl, 6-fluorohexyl and 7-fluoroheptyl. Other positions of the fluorine are not excluded.
- oxaalkyl or "alkoxy” in this application comprises straight-chain radicals of the formula CnH 2 n + i-O- (CH 2 ) m, in which n and m are each independently 1 to 6, m can also denote 0.
- aryl means an aromatic carbon group or a group derived therefrom.
- heteroaryl means "aryl” as defined above containing one or more heteroatoms.
- the polymerizable group P is a group suitable for a
- Polymerization reaction such as radical or ionic chain polymerization, polyaddition or polycondensation, or for a polymer-analogous reaction, for example, the addition or
- Condensation to a polymer backbone is suitable.
- Typical and preferred reactive mesogens are described, for example, in WO 93/22397, EP 0 261 712, DE 195 04 224, WO 95/22586, WO
- the process is used to prepare a mixture consisting of organic compounds, one or more of which are preferably mesogenic, preferably liquid crystalline.
- the mesogenic compounds preferably comprise one or more liquid crystalline compounds.
- the process product is a homogeneous, liquid-crystalline mixture.
- the process also comprises the preparation of mixtures which consist of organic substances in the homogeneous liquid phase and contain therein insoluble additives (eg small particles). The method can thus also for the
- Liquid crystal phases are modified so that they are in every known type of LCD displays, eg.
- ECB, VAN, IPS-FFS, TN, TN-TFT, STN, OCB, GH, PS-IPS, PS-FFS, PS-VA or ASM-VA displays can be used are.
- liquid-crystal mixtures may also contain further additives known to the person skilled in the art and described in the literature, such as, for example, US Pat. B. UV stabilizers such as Tinuvin ® Fa. Ciba, antioxidants,
- Free radical scavengers nanoparticles, microparticles, one or more dopants, etc. included.
- 0-15% of pleochroic dyes may be added, furthermore conductive salts, preferably ethyldimethyldodecylammonium 4-hexoxybenzoate, tetrabutylammonium tetraphenylboranate or complex salts of crown ethers (cf., for example, Haller et al., Mol.
- Suitable stabilizers and dopants which in the preparation of the liquid-crystal mixtures with the compounds of the formula I together in can be given to the mixing container are hereinafter referred to in Tables C and D.
- (0) C m H 2m + i means OC m H 2m + i or C m H 2m + i.
- nV-Vm HH Preferred mesogenic or liquid-crystalline substances which are suitable for the preparation of liquid-crystal mixtures and can be used in the purification process according to the invention are listed in particular in Tables A and B:
- CAIY-n-Om CAIY-nm
- liquid-crystalline mixtures which, in addition to one or more compounds of the formula I, contain at least one, two, three, four or more compounds from Table B.
- the mixtures contain 0-10 wt.%, In particular 0.01-5 wt.% And particularly preferably 0.01-3 wt.% Of dopants.
- Stabilizers which can be added, for example, to the liquid-crystalline mixtures in amounts of 0-10% by weight are mentioned below.
- Suitable polymerizable compounds (reactive esogens) for use in the mixtures according to the invention preferably in PSA and PS-VA applications or PS-IPS / FFS applications, are
- liquid-crystalline mixtures contain one or more reactive compounds, they are preferably used in amounts of 0.01-5% by weight.
- an initiator or a mixture of two or more initiators must be added for the polymerization. The initiator or the
- Initiator mixture is preferably added in amounts of 0.001-2 wt.% Based on the mixture.
- a suitable initiator is z. B.
- Irgacure BASF
- Irganox BASF
- liquid-crystalline mixtures contain one or more compounds selected from the group of the compounds of Table E.
- ⁇ is the optical anisotropy measured at 20 ° C and 589 nm
- the mixture with a batch size of 350 kg is 0 kg
- Alumina Merck KGaA, pore size 6-15, particle size 60-200 pm
- zeolites Merck KGaA, particle size 150-350.
- a batch size of 200 g 4 g of alumina and 1, 5 g of zeolites are used.
- the agglomerated LC mixture according to Example 1 is preferably suitable for PS-VA applications.
- Example 2 The LC mixture according to Example 2 is reacted analogously to Example 1 with 4.5 kg of aluminum oxide (from Merck KGaA, pore size 6-15, particle size 60-200 ⁇ m) and with 2.5 kg of silica gel (Merck KGaA, particle size 40-200 ⁇ m). 00 pm) with a batch size of 100 kg.
- aluminum oxide from Merck KGaA, pore size 6-15, particle size 60-200 ⁇ m
- silica gel Merck KGaA, particle size 40-200 ⁇ m. 00 pm
- Example 3 The purified mixture according to Example 2 is preferably suitable for PS-VA applications.
- Example 2 This mixture is analogous to Example 1 with 2.8 kg of alumina (Merck KGaA, pore size 6-15, particle size 60-200 ⁇ ) and with 1, 7 kg of zeolites (Merck KGaA, particle size 150-350 ⁇ ) with a
- the LC mixture according to Example 3 is preferably suitable for PS-VA applications.
- This mixture is analogously to Example 1 with 1, 7 kg of magnesium silicate (Merck KGaA, particle size 150-250 pm) and with 1, 1 kg of silica gel (Merck KGaA, particle size 63-100 ⁇ ⁇ ) with a batch size of 85 kg treated. At a batch size of 500 g, 10 g of alumina and 4.6 g of silica gel are used.
- the LC mixture according to Example 4 is preferably suitable for PS-VA applications.
- This mixture is treated analogously to Example 1 with 2.1 kg of silica gel (Merck KGaA, particle size 60-200 pm) and with 0.9 kg of zeolites (Merck KGaA, particle size 150-350 pm) with a batch size of 56 kg , At a batch size of 400 g, 20 g of silica gel and 9 g of zeolites are used.
- Example 6 The LC mixture according to Example 5 is preferably suitable for TN-TFT applications.
- Example 6 The LC mixture according to Example 5 is preferably suitable for TN-TFT applications.
- This mixture is treated analogously to Example 1 with 890 g of zeolites (Merck KGaA, particle size 150-350 pm) with a batch size of 29 kg. At a batch size of 300 g, 5.7 g of zeolites are used.
- the LC mixture according to Example 6 is preferably suitable for IPS or FFS applications.
- a batch size of 265 kg of this mixture is treated analogously to Example 1 with 10.6 kg of aluminum oxide (from Merck KGaA, pore size 6-10, particle size 40-200 ⁇ m).
- the LC mixture according to Example 7 is preferably suitable for IPS or FFS applications.
- a batch size of 530 kg of this mixture is first purified analogously to Example 1 with 10.6 kg of silica gel RP8 (Merck KGaA, pore size 6-30, particle size 10-40 ⁇ ). In addition, 4.3 kg of zeolites (Merck) are required for aftertreatment.
- Example 9 The LC mixture according to Example 8 is preferably suitable for IPS or FFS applications.
- Example 2 This mixture is analogously to Example 1 with 15 g of alumina (Merck KGaA, particle size 40-63 pm) with a batch size of 3 kg
- Alumina and 1.7 kg zeolites (Grace, particle size 100-500 pm) used.
- the LC mixture according to Example 9 is preferably suitable for TN-TFT applications.
- a batch size of 530 kg of this mixture is purified analogously to Example 1 with 10.6 kg of silica gel RP8 (Merck KGaA, pore size 6-30, particle size 0-40 pm). In addition, 4.3 kg of zeolites (from Merck KGaA, particle size 150-350 ⁇ m) are required for aftertreatment.
- the LC mixture according to Example 10 is preferably suitable for TN-TFT applications.
- a batch size of 3 kg of this mixture is purified analogously to Example 1 with 147 g of silica gel RP4 (from Merck KGaA, pore size 6-30, particle size 10-40 prn)
- Example 12 The LC mixture according to Example 11 is preferably suitable for TN-TFT applications.
- Example 12 The LC mixture according to Example 11 is preferably suitable for TN-TFT applications.
- a batch size of 143 kg of this mixture is purified analogously to Example 1 with 715 g of magnesium silicate (Merck KGaA, particle size 150-250 pm).
- the LC mixture according to Example 12 is preferably suitable for TN-TFT applications.
- Example 2 This mixture is analogously to Example 1 with 212 g of alumina (Merck KGaA, particle size 63-200 pm) with a batch size of 3 kg
- the LC mixture according to Example 13 is preferably suitable for IPS or F FS applications.
- This mixture is treated with 106 g of alumina (Merck, pore size 6-15, particle size 40-63 pm) and with 40 g of silica gel (Merck KGaA, particle size 63-100 pm) with a batch size of 1.5 kg. With a batch size of 24 kg, 1.6 kg of alumina and 0.8 kg of silica gel are used.
- the LC mixture according to Example 14 is preferably suitable for TN-TFT applications.
- a batch size of 16 kg of this mixture is purified analogously to Example 1 with 460 g of silica gel RP8 (Merck KGaA, pore size 6-30, particle size 10-40 pm)
- the LC mixture according to Example 15 is preferably suitable for VA applications.
- Example 2 This mixture is analogously to Example 1 with 2.6 kg of alumina (Merck KGaA, pore size 6-15, particle size 63-200 pm) and with 1 kg of silica gel (Merck KGaA, particle size 63-100 pm) with a
- Batch size of 132 kg treated For a batch size of 500 kg, 16 kg of alumina and 8 kg of silica gel are used.
- the LC blend of Example 16 is preferably suitable for PS-VA and PS-FFS applications.
- This mixture is treated analogously to Example 1 with 53 g of magnesium silicate (Merck KGaA, particle size 150-250 pm) at a batch size of 1 kg.
- a batch size of 16 kg of this mixture is purified analogously to Example 1 with 460 g of silica gel RP8 (from Merck KGaA, pore size 6-30, particle size 10-40 ⁇ )
- the LC mixture according to Example 18 is preferably suitable for VA applications.
- the mixing examples 1 to 18 may additionally contain one or more stabilizers, preferably one or two, and one
Abstract
Description
Claims
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EP14814761.4A EP3080599A1 (de) | 2013-12-10 | 2014-12-02 | Reinigungsvorrichtung |
CN201480067042.5A CN105980848B (zh) | 2013-12-10 | 2014-12-02 | 纯化装置 |
KR1020167018441A KR102262692B1 (ko) | 2013-12-10 | 2014-12-02 | 정제 장치 |
JP2016538096A JP2017507770A (ja) | 2013-12-10 | 2014-12-02 | 洗浄装置 |
US14/759,029 US10052566B2 (en) | 2013-12-10 | 2014-12-02 | Purification device for a liquid-crystal mixture |
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DE102013020400.3A DE102013020400A1 (de) | 2013-12-10 | 2013-12-10 | Reinigungsvorrichtung |
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EP (1) | EP3080599A1 (de) |
JP (2) | JP2017507770A (de) |
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EP3372655B1 (de) * | 2014-08-25 | 2019-12-18 | Merck Patent GmbH | Flüssigkristallmedium |
WO2020044825A1 (ja) * | 2018-08-31 | 2020-03-05 | 日本ゼオン株式会社 | 溶剤の精製方法 |
CN110922980A (zh) * | 2018-09-20 | 2020-03-27 | 江苏和成新材料有限公司 | 一种端基为氟代烷氧基的液晶材料的提纯方法 |
JP7228090B2 (ja) * | 2018-12-04 | 2023-02-24 | Dic株式会社 | 液晶組成物の製造方法、膜付基材の製造方法、液晶表示素子の製造方法及び供給装置 |
CN109852399A (zh) * | 2018-12-29 | 2019-06-07 | 阜阳欣奕华材料科技有限公司 | 一种生产混合液晶的方法 |
CN110038350A (zh) * | 2019-04-18 | 2019-07-23 | 苏州星烁纳米科技有限公司 | 纯化纳米晶溶液的装置及纯化方法 |
CN116585752B (zh) * | 2023-07-18 | 2023-10-20 | 成都百泉生物医药科技有限公司 | 一种层析柱及层析柱用振荡装置 |
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TW201545797A (zh) | 2015-12-16 |
DE102013020400A1 (de) | 2015-06-11 |
JP3226774U (ja) | 2020-07-16 |
JP2017507770A (ja) | 2017-03-23 |
EP3080599A1 (de) | 2016-10-19 |
CN105980848A (zh) | 2016-09-28 |
US20160317948A1 (en) | 2016-11-03 |
US10052566B2 (en) | 2018-08-21 |
KR102262692B1 (ko) | 2021-06-10 |
CN105980848B (zh) | 2019-06-07 |
KR20160095146A (ko) | 2016-08-10 |
TWI633916B (zh) | 2018-09-01 |
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