WO2009073641A1 - A method of forming alkoxylated flouroalcohols - Google Patents
A method of forming alkoxylated flouroalcohols Download PDFInfo
- Publication number
- WO2009073641A1 WO2009073641A1 PCT/US2008/085217 US2008085217W WO2009073641A1 WO 2009073641 A1 WO2009073641 A1 WO 2009073641A1 US 2008085217 W US2008085217 W US 2008085217W WO 2009073641 A1 WO2009073641 A1 WO 2009073641A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fluoroalcohol
- boron
- boric acid
- borate
- boron compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 33
- AQYSYJUIMQTRMV-UHFFFAOYSA-N hypofluorous acid Chemical compound FO AQYSYJUIMQTRMV-UHFFFAOYSA-N 0.000 claims description 73
- 150000001639 boron compounds Chemical class 0.000 claims description 35
- 229910052740 iodine Inorganic materials 0.000 claims description 32
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 31
- 239000011630 iodine Substances 0.000 claims description 31
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 claims description 25
- 125000002947 alkylene group Chemical group 0.000 claims description 19
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 14
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims description 12
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 claims description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 11
- -1 alkyl borate Chemical compound 0.000 claims description 11
- 229910052796 boron Inorganic materials 0.000 claims description 11
- 239000004327 boric acid Substances 0.000 claims description 9
- 239000000376 reactant Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- HSZCZNFXUDYRKD-UHFFFAOYSA-M lithium iodide Chemical compound [Li+].[I-] HSZCZNFXUDYRKD-UHFFFAOYSA-M 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 235000009518 sodium iodide Nutrition 0.000 claims description 8
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 150000001350 alkyl halides Chemical class 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- NHDIQVFFNDKAQU-UHFFFAOYSA-N tripropan-2-yl borate Chemical compound CC(C)OB(OC(C)C)OC(C)C NHDIQVFFNDKAQU-UHFFFAOYSA-N 0.000 claims description 6
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000005233 alkylalcohol group Chemical group 0.000 claims description 5
- 229910021538 borax Inorganic materials 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 5
- 239000004328 sodium tetraborate Substances 0.000 claims description 5
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 5
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 claims description 5
- XZXYQEHISUMZAT-UHFFFAOYSA-N 2-[(2-hydroxy-5-methylphenyl)methyl]-4-methylphenol Chemical compound CC1=CC=C(O)C(CC=2C(=CC=C(C)C=2)O)=C1 XZXYQEHISUMZAT-UHFFFAOYSA-N 0.000 claims description 4
- XDVOLDOITVSJGL-UHFFFAOYSA-N 3,7-dihydroxy-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound O1B(O)OB2OB(O)OB1O2 XDVOLDOITVSJGL-UHFFFAOYSA-N 0.000 claims description 4
- UNMYWSMUMWPJLR-UHFFFAOYSA-L Calcium iodide Chemical compound [Ca+2].[I-].[I-] UNMYWSMUMWPJLR-UHFFFAOYSA-L 0.000 claims description 4
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- 229940107816 ammonium iodide Drugs 0.000 claims description 4
- UYANAUSDHIFLFQ-UHFFFAOYSA-N borinic acid Chemical compound OB UYANAUSDHIFLFQ-UHFFFAOYSA-N 0.000 claims description 4
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims description 4
- 229910001640 calcium iodide Inorganic materials 0.000 claims description 4
- 229940046413 calcium iodide Drugs 0.000 claims description 4
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 4
- VGTPKLINSHNZRD-UHFFFAOYSA-N oxoborinic acid Chemical compound OB=O VGTPKLINSHNZRD-UHFFFAOYSA-N 0.000 claims description 4
- 229960004839 potassium iodide Drugs 0.000 claims description 4
- 229940083599 sodium iodide Drugs 0.000 claims description 4
- LGQXXHMEBUOXRP-UHFFFAOYSA-N tributyl borate Chemical compound CCCCOB(OCCCC)OCCCC LGQXXHMEBUOXRP-UHFFFAOYSA-N 0.000 claims description 4
- AJSTXXYNEIHPMD-UHFFFAOYSA-N triethyl borate Chemical compound CCOB(OCC)OCC AJSTXXYNEIHPMD-UHFFFAOYSA-N 0.000 claims description 4
- LTEHWCSSIHAVOQ-UHFFFAOYSA-N tripropyl borate Chemical compound CCCOB(OCCC)OCCC LTEHWCSSIHAVOQ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052810 boron oxide Inorganic materials 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- 238000006243 chemical reaction Methods 0.000 description 24
- 239000003054 catalyst Substances 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000002585 base Substances 0.000 description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
- 239000004094 surface-active agent Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 229910015900 BF3 Inorganic materials 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- 150000001298 alcohols Chemical class 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 5
- 125000001153 fluoro group Chemical group F* 0.000 description 5
- 238000011065 in-situ storage Methods 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000005647 linker group Chemical group 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000006227 byproduct Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N Vilsmeier-Haack reagent Natural products CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- GDTSJMKGXGJFGQ-UHFFFAOYSA-N 3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical class O1B([O-])OB2OB([O-])OB1O2 GDTSJMKGXGJFGQ-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- AWMVMTVKBNGEAK-UHFFFAOYSA-N Styrene oxide Chemical compound C1OC1C1=CC=CC=C1 AWMVMTVKBNGEAK-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001516 alkali metal iodide Inorganic materials 0.000 description 1
- 229910001619 alkaline earth metal iodide Inorganic materials 0.000 description 1
- 239000006265 aqueous foam Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 150000002496 iodine Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/02—Preparation of ethers from oxiranes
- C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/12—Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/13—Saturated ethers containing hydroxy or O-metal groups
Definitions
- Hydrocarbon surfactants are very common and are the workhorse materials for making aqueous foams and wetting surfaces, among other things. Surfactants, in general, produce these effects by lowering the surface tension of the liquid in which they are dissolved. Hydrocarbon surfactants, however, lower the surface tension of water to only about 30 dynes/cm (0.03 N/m). To provide lower surface tensions, fluoro surfactants are often used.
- Fluoro surfactants including amphiphilic fluoropolymers, can give surface tensions of less than 20 dynes/cm (0.02 N/m), which are necessary to better wet low energy surfaces, for example.
- fluoro surfactants can be classified as anionic (containing negative charge), cationic (containing positive charge), amphoteric (having both positive and negative charges) and nonionic (having no charge).
- Nonionic fluoro surfactants are particularly desirable due, not only to the very low surface tension obtainable, but also to their efficacy in extreme conditions such as high acidity or alkalinity, high salt levels (ionic strength), elevated temperatures, etc. They are also very resilient and not easily degraded.
- Nonionic fluoro surfactant is an alkoxylated fluoroalcohol.
- the fluoroalcohol molecule itself is hydrophobic so that it is insoluble in water or other aqueous fluids. Alkoxylation of the fluoroalcohol adds a hydrophilic portion to the molecule so that it is water soluble and surface active.
- Alkylene oxides such as ethylene oxide and propylene oxide, are reactive toward most hydroxyl functional groups such as the terminal -OH of the fluoroalcohol or alkoxylated fluoroalcohol.
- catalysts are employed to aid in the alkoxylation reaction.
- Existing catalysts for alkoxylating fluoroalcohols include boron trifluoride (BF 3 or BF 3 -etherate), borohydrides, etc. These materials have certain shortcomings, however. Boron trifluoride is both toxic and corrosive and presents a safety and handling concern. Furthermore, it has a fairly low reactivity, broad alkoxylate distributions and requires excessive residual starting materials.
- Boron trifluoride also produces undesirable by-products, namely, HF and 1,4-dioxane.
- Borohydride catalysts for alkoxylation of fluoroalcohols are effective, but only with the addition of other additives, and are sensitive to impurities. Without the proper balance of additives and low impurities, borohydride catalysis for alkoxylating fluoroalcohols can be slow or fail outright. Borohydrides also present a handling and safety concern, because the borohydride powders are highly flammable and produce highly flammable hydrogen gas as a reaction byproduct.
- a method of forming an alkoxylated fluoroalcohol is accomplished by combining a boron compound having or providing at least one boron-oxygen bond and an iodine source. These are provided with reactants of a fluoroalcohol and an alkylene oxide in the presence of a base. The reactants are allowed to react to form an alkoxylated fluoroalcohol reaction product.
- the boron compound which may provide three (3) boron- oxygen bonds, is an oxide of boron, an alkyl borate, a boric acid, a boric acid anhydride, a boronic acid, a borinic acid or salts or esters of said acids or combinations of these.
- boric acid H3BO3
- a boric acid anhydride meta boric acid (HBO 2 )
- tetra boric acid H 2 B 4 O 7
- boron oxide B 2 O 3
- trimethyl borate triethyl borate, triisopropyl borate, tripropyl borate, tributyl borate, sodium tetraborate, potassium tetraborate or combinations of these.
- the boron compound may be used in an amount of from about 0.01 mole% to about 20 mole% by total moles of fluoroalcohol.
- the iodine source may be selected from at least one of lithium iodide, sodium iodide, potassium iodide, calcium iodide, ammonium iodide, elemental iodine or combinations of these. In certain embodiments, the iodine source may be used in an amount of from about 0.05% to about 10%% by weight of the fluoroalcohol.
- the fluoroalcohol may have the structure of F(CF 2 ) m -OH or F(CF 2 ) m -A-OH, wherein m is from 2 to 20 and A is a
- R 1 and R 4 are each independently selected from one of hydrogen, a halogen or an alkyl group containing from 1-30 carbon atoms, and R 2 and R 3 are each independently selected from an alkylene group containing from 2 to 30 carbon atoms.
- the alkylene oxide may have the structure:
- R 9 , R 10 , R 11 and R 12 are each independently one of hydrogen, an alkyl group, an alkyl alcohol, an alkyl halide or an allyl ether.
- the alkylene oxide is used in an amount of from about 1 mole% to about 100 mole% by total moles of the fluoroalcohol and boron compound.
- the boron compound is initially combined with a non- fluoroalcohol that is subsequently substituted with the fluoroalcohol.
- the fluoroalcohol may be a fluoroalcohol having the generalized structure according to Equations (1) or (2) below:
- F(CF 2 ) m denotes a perfluorinated alkyl group, where m is usually, but not necessarily, 2-20, and more typically 4-14. In certain embodiments m may be from 2 to
- m may be from 2 to 6.
- the alkyl group F(CF 2 ) m is typically linear but may be branched, as well.
- the linking group A may be a connecting group of a -(CH 2 ) n -, which may be branched or linear,
- the fluoroalcohol may include one or more hydrogens substituted for fluorine, such as the group H(CF 2 ) m for example.
- the fluoroalcohols may have molecular weights of from about 200 to about 2000 g/mol, more typically from about 300 to about 500 g/mol.
- suitable fluoroalcohols are those described in U.S. Patent Nos. 4,490,561; 5,590,561 and 5,608,116, which are each incorporated herein by reference in their entireties for all purposes.
- the alkoxylating reaction is carried out using a catalyst system that includes a boron compound.
- Most alkoxylating agents are not appreciably soluble in the fluoroalcohols.
- the boron compound may complex with the alkoxylating agent facilitating incorporation and reaction of the alkoxylating with the fluoroalcohol.
- the catalyst or catalytic properties of the boron compound may be formed or provided in- situ, with the same or similar functionality as borohydride or boron trifluoride catalysts. As used herein, "in-situ" refers to the formation of the catalyst in the presence of the fluoroalcohol or at least one of the reactants.
- the boron compound is one that has or provides at least one boron-oxygen bond.
- the boron compound may have or provide one (1) to four (4) boron-oxygen bonds per boron atom.
- the boron compound may be added to the fluoroalcohol or a stand-in alcohol to provide or create a catalyst species capable of carrying out the alkoxylating reactions.
- the boron compound may have, but is not limited to, the general structure shown in Equation (3) below:
- R 5 and R 6 are each independently H, an alkyl group (e.g. CH 3 , CH 3 CH 2 , etc.), an aryl, an alkylaryl, an alkyl halide, a halogen (e.g. F, Cl, Br, I), or -OR 8 , and wherein R 7 and R 8 are each independently H, an alkyl group, a carbonyl, a carboxyl, an aryl or an alkylaryl.
- R 7 and R 8 are each independently H, an alkyl group, a carbonyl, a carboxyl, an aryl or an alkylaryl.
- the boron compound of Equation 3 is shown as having three substituents, the boron compound also has an empty orbital that can complex with a fourth molecule, which is typically neutral or uncharged.
- This fourth molecule may include an alcohol, such as methanol, ethanol, etc., or an ether, such as diethyl ether, tetrahydrofur
- the boron compound may an oxide of boron, an alkyl borate, a boric acid, a boric acid anhydride, a boronic acid, a borinic acid or salts or esters of said acids or combinations of these.
- Examples of the boron compound may include boric acid
- boron compound may provide the boron-oxygen bond in-situ.
- the boron compound may be used in an amount of from about 0.01 mole% to about 20 mole% by total moles of fluoroalcohol, more particularly from about 0.05 mole% to about 5 mole% by total moles of fluoroalcohol.
- An iodine co-catalyst is also used in the catalyst system.
- the iodine co-catalyst is provided from an iodine source, which may be an alkali metal iodide, alkaline earth metal iodide or elemental iodine and combinations of these.
- iodine source may be an alkali metal iodide, alkaline earth metal iodide or elemental iodine and combinations of these.
- iodine salts may be useful as the iodine source.
- suitable iodine sources include lithium iodide, sodium iodide, potassium iodide, calcium iodide, ammonium iodide, elemental iodine or combinations of these.
- the iodine source is used in an amount of from about 0.05% to about 10% by weight of the fluoroalcohol, more particularly from about 0.1% to about 2% by weight of the fluoroalcohol. If the iodine source is other than sodium iodide (NaI) or elemental iodine (I 2 ), higher amounts of the iodine source may be used. In certain instances, approximately twice as much of the other iodine sources may be used.
- an alkoxylating agent of an alkylene oxide used for the fluoroalcohol alkoxylation may have the general structure of Equation (4) below:
- R 9 , R 10 , R 11 and R 12 are each independently one of hydrogen, an alkyl group, an alkyl alcohol, an alkyl halide, an aryl, an alkylaryl or an allyl ether.
- Particularly useful are those alkylene oxides of ethylene oxide, propylene oxide, butylene oxide, glycidol, epichlorohydrin, styrene oxide, oxetane, tetrahydrofuran, 1,4-dioxane, allyl glycidyl ether, fluorinated cyclic ethers (e.g., fluorinated ethylene oxide, fluorinated propylene oxide, etc.) or mixtures of these.
- Ethylene oxide and propylene oxide are particularly useful in carrying out the alkoxylation reactions.
- suitable alkylene oxides for use in the alkoxylation reactions are described in U.S. Patent Application Publication No. 2006/0069220A1 and U.S. Patent No. 5,608,116, which are each incorporated herein by reference.
- the alkoxylating agent may be used in an amount of from about 1 mole% to about
- the alkoxylating agent may be used in stoichiometric amounts to provide the desired degree of alkoxylation.
- an alkali or base is also used in the reaction. While not wanting to be bound by any particular theory, it is believed that the base deprotonates the fluoroalcohol to allow it to react with the boron compound to form a borate ester in situ.
- suitable bases include metal hydroxides, such sodium hydroxide (NaOH), sodium hydride (NaH), and those having the general structure R-O-Na, where R is an alkyl, such as sodium methylate, sodium ethoxide, etc.
- Other bases may include KOH, Ca(OH) 2 , Mg(OH) 2 , etc., however, NaOH has been shown to work particularly well in testing.
- the base may be used in an amount of 0.05% to about 5% by weight of the fluoroalcohol, more particularly from about 1% to about 5% by weight of the fluoroalcohol.
- reaction can be carried out under an inert atmosphere (nitrogen, argon, etc.) or in air.
- the reaction can also be carried out under a reduced pressure or under vacuum or under reactant pressure (e.g., ethylene oxide vapor pressure).
- reactant pressure e.g., ethylene oxide vapor pressure
- solvents may be combined with the fluoroalcohol in certain instances, such as for temperature control and to facilitate solubility of the catalyst system, reactants or reaction products.
- suitable solvents include, polar and non-polar aprotic solvents such as dimethyl sulfoxide, N-methyl pyrrolidone, N 5 N- dimethyl formamide, glyme, diglyme, etc., acetone, acetonitrile, hydrocarbons, glycol ether esters, esters, fluorocarbon solvents, etc. Water is generally excluded from alkoxylation reactions by a drying process due to its initiation of unwanted, homo- polymerization.
- polar and non-polar aprotic solvents such as dimethyl sulfoxide, N-methyl pyrrolidone, N 5 N- dimethyl formamide, glyme, diglyme, etc., acetone, acetonitrile, hydrocarbons, glycol ether esters, esters, fluorocarbon solvents, etc. Water is generally excluded from alkoxylation reactions by a drying process due to its initiation of unwanted, homo- polymerization.
- the iodine source and any base may be initially added to the fluoroalcohol.
- NaOH and other bases may form water. It may be desirable to remove such water from the fluoroalcohol prior to adding the boron compound. Water may compete against the fluoroalcohol and react with the boron compound to produce unwanted side products or sub-optimal catalytic species, or hamper the desired in situ catalyst formation. It may be desirable to therefore add the NaOH or other base prior to the salts and other components for this reason as well.
- the solution may then be heated to remove any water to dry the fluoroalcohol.
- the iodine source may then be added followed by addition of the boron compound.
- water may also be formed from the reaction of boric acid and base. This water may also be removed through heating of the solution. After any drying, the alkoxylating agent may be added. This may be added gradually as the reaction is carried out.
- the reaction temperatures may be kept at from about ambient to 200 0 C, with typical reaction temperatures being from about 90 0 C to about 150 0 C. Mixing and heating, if any, may be continued during the reaction.
- the use of an alcohol that is a non-fluoroalcohol may be used.
- this "stand-in" alcohol is used during catalyst synthesis using the same procedures or steps as with the fluoroalcohol described previously.
- the fluoroalcohol is then added to the mixture, with the fluoroalcohol displacing the non- fluoroalcohol, such as through evaporation or transesterification.
- the alcohols are typically low molecular weight alcohols, that have low boiling points so that they can be readily removed, such as through heating and evaporation. When removed in this manner, the volatile alcohols carry away residual water, further drying the reaction mixture.
- suitable high volatility alcohols are methanol, ethanol, n-propanol, isopropyl alcohol, butanol, etc.
- the stand-in alcohol may be used in an amount of from greater than 0 to about 5 mole% or more based on boron. Typically, the stand-in alcohol may be used in an amount of from about 3 mole% to about 4 mole%.
- the alkoxylating reaction can be illustrated by the reaction shown in Equations (5) to (8) below:
- Rf is a perfluoralkyl, such as F(CF 2 ) m
- M is the boron catalyst species, which may or may not carry a formal charge
- A is the linking group described from Equation 2
- X may be H or an alkyl group (e.g., -CH 3 ), an alkyl alcohol, an alkyl halide, an aryl, an alkylaryl or an allyl ether, depending on the alkylene oxide used for alkoxylation
- n is an integer, which may range from about 1 to 100 or more.
- Equations (5)-(9) certain exchange reactions, for example of a proton or catalyst species, are omitted, but are recognized to occur between various alcohol or alcohol ethoxylate molecules.
- the linking group A may also be absent from the above equations such as when fluoroalcohols having the structure of Equation 1 are used.
- the alkoxylated fluoroalcohol may then have the general formula of Equation (9) below:
- alkoxylated fluoroalcohols formed from the above reactions are non-ionic alkoxylated fluoroalcohol products.
- the alkoxylated fluoroalcohols may also be subsequently derivatized to make anionic fluoroalcohols, such as through the use of, for example, chloro sulfonic acid and phosphorous pentoxide to make ether sulfates and phosphates, respectively, or other products, which may be anionic.
- Further processing may be also conducted on the alkoxylated fluoroalcohols, such as catalyst removal, such as by filtration, distillation and other separation techniques. Dilution of the reaction product with solvents, such as water, alcohols, glycols, glycol ethers, etc., and mixtures of the same, may also be used if desired for final products.
- alkoxylated fluoroalcohols prepared in accordance with the invention are useful in formulating paints and coatings, inks, waxes, polishes, anti-corrosion coatings, leveling agents, wetting agents, oil field chemicals, etc.
- the method of invention avoids the use of borohydride and boron trifluoride catalysts, while providing the generally the same degree or better reactivity.
- the boron compounds and other components used in the method of the invention are readily available and generally easily handled and safe to transport and store.
- resulting alcohols from borate ester transesterification that are formed during the method of the invention may be readily driven off. This is beneficial in that the evaporating alcohols entrain water, which can react with the alkoxylating agent (e.g. ethylene oxide) to produce polyalkylene oxide homopolymers
- the alkoxylating agent e.g. ethylene oxide
- a 141.3 g quantity of a fluoroalcohol having no solubility in water with the same general formula as that of Example 1 and having an average molecular weight of about 364 g/mol was charged to a reactor as described in Example 1.
- To the reactor was added 0.7 g NaOH, which was then heated to 125 0 C under a nitrogen purge to dissolve the NaOH and dry the fluoroalcohol.
- 0.7 g iodine and 0.8 g sodium iodide were added as the reactor cooled.
- 3.9 ml of triisopropyl borate was added, and the reactor was again heated to 100 0 C for 25 min, and then further heated to the reaction temperature of about 14O 0 C.
- Example 2 The procedures of Example 2 were repeated except that boric acid was used in place of triisopropyl borate. After charging 141.4 g of fluoroalcohol to the reactor, 0.8 g
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CN200880117439.5A CN101874010B (en) | 2007-12-03 | 2008-12-02 | A method of forming alkoxylated flouroalcohols |
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AU2008333995A AU2008333995B2 (en) | 2007-12-03 | 2008-12-02 | A method of forming alkoxylated fluoroalcohols |
DK08856599.9T DK2215042T3 (en) | 2007-12-03 | 2008-12-02 | PROCEDURE FOR PREPARING ALCOXYLERED FLUORAL ALCOHOLS |
JP2010537008A JP5571564B2 (en) | 2007-12-03 | 2008-12-02 | Process for producing alkoxylated fluoroalcohol |
CA2702519A CA2702519C (en) | 2007-12-03 | 2008-12-02 | A method of forming alkoxylated fluoroalcohols |
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AU2010242869B2 (en) * | 2009-04-30 | 2016-06-16 | The Chemours Company Fc, Llc. | Process for the alkoxylation of alcohols |
WO2018015417A1 (en) | 2016-07-20 | 2018-01-25 | Solvay Specialty Polymers Italy S.P.A. | Method for manufacturing polyalkoxylated polymers |
US11492318B2 (en) | 2017-05-19 | 2022-11-08 | Etna-Tec, Ltd. | Methods for making functionalized fluorinated monomers, fluorinated monomers, and compositions for making the same |
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---|---|---|---|---|
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5002678A (en) * | 1990-06-29 | 1991-03-26 | Olin Corporation | Lubricants for heat transfer fluids |
US5608116A (en) * | 1994-06-21 | 1997-03-04 | E. I. Du Pont De Nemours And Company | Process for the alkoxylation of fluorinated alcohols |
JP2005046749A (en) * | 2003-07-29 | 2005-02-24 | Dai Ichi Kogyo Seiyaku Co Ltd | Catalyst for alkoxylation and method for manufacturing alkylene oxide addition product using it |
US20060069220A1 (en) * | 2004-09-28 | 2006-03-30 | Meurs Jan Hermen H | Process for preparing an alkoxylated alcohol or phenol |
Family Cites Families (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2600378A (en) * | 1950-04-14 | 1952-06-17 | Eastman Kodak Co | Preparation of tetraethyl pyrophosphate |
US2723999A (en) | 1954-01-15 | 1955-11-15 | American Cyanamid Co | Fluorinated alcohol-ethylene oxide condensates |
US3359331A (en) | 1965-11-10 | 1967-12-19 | Exxon Research Engineering Co | Secondary alcohol ethoxylation |
DD111522A3 (en) * | 1970-10-23 | 1975-02-20 | ||
US3676477A (en) | 1970-11-30 | 1972-07-11 | Du Pont | Esters of pentavalent and trivalent antimony with a polyhydroxy compound and the process for making the same |
US3944586A (en) | 1971-12-03 | 1976-03-16 | Richard Norris Knowles | Preparation of salts of antimony (V) esters |
GB1410328A (en) * | 1971-12-21 | 1975-10-15 | Unilever Ltd | Alkoxylation process |
US3944653A (en) | 1972-08-30 | 1976-03-16 | Occidental Petroleum Corporation | Process for preparing high purity antimony trichloride and antimony oxide from stibnite ores |
US3948668A (en) | 1974-03-15 | 1976-04-06 | E. I. Du Pont De Nemours And Company | Fluorocarbon-containing printing ink and process for image printing |
SU570590A1 (en) * | 1974-08-05 | 1977-08-30 | Предприятие П/Я А-7850 | Method of preparing oxyalkylated fluorated alcohols |
US3980715A (en) | 1975-03-21 | 1976-09-14 | Diamond Shamrock Corporation | Nonionic fluorochemical surfactants |
US4169104A (en) | 1977-03-18 | 1979-09-25 | The Harshaw Chemical Company | Method of preparing salts of esters of pentavalent antimony |
US4287118A (en) | 1978-08-23 | 1981-09-01 | Associated Lead Inc. | Antimony (V) mercaptides as processing stabilizers for vinyl halide resins and method of manufacturing same |
US4240956A (en) | 1979-06-20 | 1980-12-23 | Stauffer Chemical Company | Tri(dibromoneopentyl) antimonite flame retardants |
US4408043A (en) | 1982-03-08 | 1983-10-04 | Nalco Chemical Company | Fluorocarbon surfactants |
US4483941A (en) | 1982-09-02 | 1984-11-20 | Conoco Inc. | Catalysts for alkoxylation reactions |
US4456697A (en) | 1982-09-23 | 1984-06-26 | Conoco Inc. | Catalysts for alkoxylation reactions |
US4490561A (en) | 1983-10-13 | 1984-12-25 | Conoco Inc. | Method for alkoxylating fluorinated alcohols |
US4594200A (en) | 1984-11-15 | 1986-06-10 | Halliburton Company | Compositions for increasing hydrocarbon production from subterranean formations |
US5057628A (en) | 1987-12-17 | 1991-10-15 | Shell Oil Company | Alkoxylation process catalyzed by compounds of the rare earth elements |
DE3814849A1 (en) | 1988-05-02 | 1989-11-16 | Henkel Kgaa | USE OF ESTERS OF TITANIC AND / OR ZIRCONIC ACIDS AS CATALYSTS FOR ETHOXYLATION OR. PROPOXYLATION |
US4992211A (en) | 1988-11-30 | 1991-02-12 | Sandoz Ltd. | Alkylene oxide-containing amphoteric surfactants |
US5026923A (en) | 1989-08-31 | 1991-06-25 | Shell Oil Company | Alkoxylation process catalyzed by borate salts of the rare earth elements |
US5041576A (en) | 1989-12-07 | 1991-08-20 | Wasfi Sadio H | Antimony oxo-metalate complexes |
WO1991018038A1 (en) | 1990-05-11 | 1991-11-28 | Asahi Glass Company Ltd. | Process for producing polyoxyalkylene compound |
DE4117935A1 (en) | 1991-05-31 | 1992-12-03 | Hoechst Ag | METHOD FOR PRODUCING ALKOXYLATES WITH A NARROW HOMOLOGICAL DISTRIBUTION USING ANTIMONE PENTAHALOGENIDE COMPLEXES AS A CATALYST |
US5852148A (en) | 1991-07-10 | 1998-12-22 | Minnesota Mining & Manufacturing Company | Perfluoroalkyl halides and derivatives |
US6048952A (en) | 1991-07-10 | 2000-04-11 | 3M Innovative Properties Company | Perfluoroalkyl halides and derivatives |
US5567857A (en) | 1994-06-21 | 1996-10-22 | E. I. Du Pont De Nemours And Company | Fluoroalkylethoxylate compositions having enhanced water solubility |
US5882541A (en) | 1996-11-04 | 1999-03-16 | Hans Achtmann | Biodegradable foam compositions for extinguishing fires |
US6340779B1 (en) | 1996-11-28 | 2002-01-22 | Asahi Glass Company Ltd. | Cement admixture, concrete, and process for producing fluorooxyalylene compounds |
JPH10287689A (en) | 1997-04-11 | 1998-10-27 | Tanaka Eng Kk | Production of antimony ethylene glyoxide |
DE19807991A1 (en) | 1998-02-26 | 1999-09-02 | Clariant Gmbh | Alkoxylation catalyst |
US6028230A (en) | 1998-06-05 | 2000-02-22 | Arco Chemical Technology, L.P. | Epoxide polymerization process |
IT1303769B1 (en) | 1998-11-19 | 2001-02-23 | Enichem Spa | CATALYST AND ITS USE FOR THE SYNTHESIS OF POLYETERS POLYETERS. |
US6455459B1 (en) | 1999-11-18 | 2002-09-24 | Union Carbide Chemicals & Plastics Technology Corporation | Antimony catalyst compositions |
US6998465B2 (en) | 2001-09-28 | 2006-02-14 | Nof Corporation | Process for producing boric ester compound, electrolyte for electrochemical device, and secondary battery |
ES2327722T3 (en) * | 2001-11-19 | 2009-11-03 | Shell Internationale Research Maatschappij B.V. | PROCEDURE FOR THE ALCOXILATION OF ORGANIC COMPOUNDS. |
US8946486B2 (en) * | 2007-12-03 | 2015-02-03 | Tyco Fire & Security Gmbh | Method of forming alkoxylated fluoroalcohols |
US8058480B2 (en) | 2009-04-30 | 2011-11-15 | E. I. Du Pont De Nemours And Company | Process for the alkoxylation of alcohols |
US8067329B2 (en) * | 2009-04-30 | 2011-11-29 | E. I. Du Pont De Nemours And Company | Boron-based catalysts |
US8058481B2 (en) * | 2009-04-30 | 2011-11-15 | E.I. Du Pont De Nemours And Company | Alkyl alkoxylates containing unique end groups |
-
2008
- 2008-12-01 US US12/325,329 patent/US8946486B2/en active Active
- 2008-12-02 EP EP08856599.9A patent/EP2215042B1/en active Active
- 2008-12-02 ES ES08856599.9T patent/ES2477540T3/en active Active
- 2008-12-02 JP JP2010537008A patent/JP5571564B2/en not_active Expired - Fee Related
- 2008-12-02 CA CA2702519A patent/CA2702519C/en active Active
- 2008-12-02 KR KR1020107008073A patent/KR101597297B1/en active IP Right Grant
- 2008-12-02 AU AU2008333995A patent/AU2008333995B2/en active Active
- 2008-12-02 DK DK08856599.9T patent/DK2215042T3/en active
- 2008-12-02 WO PCT/US2008/085217 patent/WO2009073641A1/en active Application Filing
- 2008-12-02 CN CN200880117439.5A patent/CN101874010B/en active Active
-
2015
- 2015-02-03 US US14/613,222 patent/US9950978B2/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5002678A (en) * | 1990-06-29 | 1991-03-26 | Olin Corporation | Lubricants for heat transfer fluids |
US5608116A (en) * | 1994-06-21 | 1997-03-04 | E. I. Du Pont De Nemours And Company | Process for the alkoxylation of fluorinated alcohols |
JP2005046749A (en) * | 2003-07-29 | 2005-02-24 | Dai Ichi Kogyo Seiyaku Co Ltd | Catalyst for alkoxylation and method for manufacturing alkylene oxide addition product using it |
US20060069220A1 (en) * | 2004-09-28 | 2006-03-30 | Meurs Jan Hermen H | Process for preparing an alkoxylated alcohol or phenol |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2010242869B2 (en) * | 2009-04-30 | 2016-06-16 | The Chemours Company Fc, Llc. | Process for the alkoxylation of alcohols |
WO2014090649A1 (en) | 2012-12-11 | 2014-06-19 | Solvay Specialty Polymers Italy S.P.A. | Process for the alkoxylation of (per)fluoropolyether alcohols |
CN104884502A (en) * | 2012-12-11 | 2015-09-02 | 索尔维特殊聚合物意大利有限公司 | Process for the alkoxylation of (per)fluoropolyether alcohols |
US9334213B2 (en) | 2012-12-11 | 2016-05-10 | Solvay Specialty Polymers Italy S.P.A. | Process for the alkoxylation of (per) fluoropolyether alcohols |
WO2018015417A1 (en) | 2016-07-20 | 2018-01-25 | Solvay Specialty Polymers Italy S.P.A. | Method for manufacturing polyalkoxylated polymers |
US10968312B2 (en) | 2016-07-20 | 2021-04-06 | Solvay Specialty Polymers Italy S.P.A. | Method for manufacturing polyalkoxylated polymers |
US11492318B2 (en) | 2017-05-19 | 2022-11-08 | Etna-Tec, Ltd. | Methods for making functionalized fluorinated monomers, fluorinated monomers, and compositions for making the same |
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EP2215042A1 (en) | 2010-08-11 |
ES2477540T3 (en) | 2014-07-17 |
AU2008333995A1 (en) | 2009-06-11 |
JP5571564B2 (en) | 2014-08-13 |
CA2702519C (en) | 2016-04-26 |
DK2215042T3 (en) | 2014-07-07 |
KR101597297B1 (en) | 2016-02-24 |
CA2702519A1 (en) | 2009-06-11 |
AU2008333995B2 (en) | 2014-09-25 |
CN101874010B (en) | 2014-11-12 |
US8946486B2 (en) | 2015-02-03 |
JP2011505423A (en) | 2011-02-24 |
EP2215042A4 (en) | 2011-11-16 |
KR20100098366A (en) | 2010-09-06 |
CN101874010A (en) | 2010-10-27 |
US20090143621A1 (en) | 2009-06-04 |
US20150148565A1 (en) | 2015-05-28 |
US9950978B2 (en) | 2018-04-24 |
EP2215042B1 (en) | 2014-04-02 |
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