NO743987L - - Google Patents

Info

Publication number: NO743987L
Authority: NO; Norway
Prior art keywords: mixture according; mixture; group; carbon atoms; solvent
Prior art date: 1973-11-05

Application number

NO743987A

Other languages

English (en)

Norwegian (no)

Inventor

J T Mccullins

J J Monaghan

Original Assignee

Nat Res Dev

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1973-11-05

Filing date

1974-11-05

Publication date

1975-06-02

1974-11-05 Application filed by Nat Res Dev filed Critical Nat Res Dev

1975-06-02 Publication of NO743987L publication Critical patent/NO743987L/no

Links

239000000203 mixture Substances 0.000 claims description 132
125000004432 carbon atom Chemical group C* 0.000 claims description 58
239000002904 solvent Substances 0.000 claims description 57
239000004094 surface-active agent Substances 0.000 claims description 51
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 48
239000003973 paint Substances 0.000 claims description 47
150000002148 esters Chemical class 0.000 claims description 37
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 28
150000001875 compounds Chemical class 0.000 claims description 27
239000003349 gelling agent Substances 0.000 claims description 27
-1 hydroxypropoxy groups Chemical group 0.000 claims description 27
125000000217 alkyl group Chemical group 0.000 claims description 16
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 14
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 12
239000002253 acid Substances 0.000 claims description 12
125000003158 alcohol group Chemical group 0.000 claims description 12
125000002947 alkylene group Chemical group 0.000 claims description 11
230000015572 biosynthetic process Effects 0.000 claims description 11
229920002678 cellulose Polymers 0.000 claims description 11
235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 11
229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 10
239000001913 cellulose Substances 0.000 claims description 10
125000001033 ether group Chemical group 0.000 claims description 10
150000002576 ketones Chemical class 0.000 claims description 10
239000001863 hydroxypropyl cellulose Substances 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical group FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 9
238000004090 dissolution Methods 0.000 claims description 8
239000003960 organic solvent Substances 0.000 claims description 8
125000001931 aliphatic group Chemical group 0.000 claims description 7
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical group FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
230000002745 absorbent Effects 0.000 claims description 6
239000002250 absorbent Substances 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 6
239000000839 emulsion Substances 0.000 claims description 6
125000000524 functional group Chemical group 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 claims description 4
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 claims description 3
125000003342 alkenyl group Chemical group 0.000 claims description 3
238000010790 dilution Methods 0.000 claims description 3
239000012895 dilution Substances 0.000 claims description 3
150000002170 ethers Chemical class 0.000 claims description 3
239000001023 inorganic pigment Substances 0.000 claims description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 claims description 3
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 3
238000005406 washing Methods 0.000 claims description 3
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 2
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 claims description 2
NQBXSWAWVZHKBZ-UHFFFAOYSA-N 2-butoxyethyl acetate Chemical group CCCCOCCOC(C)=O NQBXSWAWVZHKBZ-UHFFFAOYSA-N 0.000 claims description 2
229940093475 2-ethoxyethanol Drugs 0.000 claims description 2
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 claims description 2
YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 claims description 2
QMAQLCVJIYANPZ-UHFFFAOYSA-N 2-propoxyethyl acetate Chemical compound CCCOCCOC(C)=O QMAQLCVJIYANPZ-UHFFFAOYSA-N 0.000 claims description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical group O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
229910052814 silicon oxide Inorganic materials 0.000 claims description 2
125000005113 hydroxyalkoxy group Chemical group 0.000 claims 4
101100440696 Caenorhabditis elegans cor-1 gene Proteins 0.000 claims 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 1
125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
125000006551 perfluoro alkylene group Chemical group 0.000 claims 1
ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 claims 1
CIBMHJPPKCXONB-UHFFFAOYSA-N propane-2,2-diol Chemical compound CC(C)(O)O CIBMHJPPKCXONB-UHFFFAOYSA-N 0.000 claims 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 1
239000000499 gel Substances 0.000 description 27
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
230000008901 benefit Effects 0.000 description 13
239000003795 chemical substances by application Substances 0.000 description 13
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
125000001153 fluoro group Chemical group F* 0.000 description 10
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 8
125000001183 hydrocarbyl group Chemical group 0.000 description 8
239000000463 material Substances 0.000 description 8
239000011877 solvent mixture Substances 0.000 description 8
235000010980 cellulose Nutrition 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
229920000180 alkyd Polymers 0.000 description 5
235000014113 dietary fatty acids Nutrition 0.000 description 5
125000004185 ester group Chemical group 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
150000004665 fatty acids Chemical class 0.000 description 5
239000000443 aerosol Substances 0.000 description 4
238000009472 formulation Methods 0.000 description 4
229910021485 fumed silica Inorganic materials 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
125000002768 hydroxyalkyl group Chemical group 0.000 description 4
239000000377 silicon dioxide Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
125000002091 cationic group Chemical group 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000002245 particle Substances 0.000 description 3
229920002635 polyurethane Polymers 0.000 description 3
239000004814 polyurethane Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 2
SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 2
SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
230000001588 bifunctional effect Effects 0.000 description 2
DKPFZGUDAPQIHT-UHFFFAOYSA-N butyl acetate Chemical compound CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 2
239000004568 cement Substances 0.000 description 2
239000004567 concrete Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
239000000975 dye Substances 0.000 description 2
239000004210 ether based solvent Substances 0.000 description 2
NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
239000000693 micelle Substances 0.000 description 2
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
230000008569 process Effects 0.000 description 2
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
YKYONYBAUNKHLG-UHFFFAOYSA-N propyl acetate Chemical compound CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 2
150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
238000005201 scrubbing Methods 0.000 description 2
230000003381 solubilizing effect Effects 0.000 description 2
230000008719 thickening Effects 0.000 description 2
239000002562 thickening agent Substances 0.000 description 2
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
OZXIZRZFGJZWBF-UHFFFAOYSA-N 1,3,5-trimethyl-2-(2,4,6-trimethylphenoxy)benzene Chemical compound CC1=CC(C)=CC(C)=C1OC1=C(C)C=C(C)C=C1C OZXIZRZFGJZWBF-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
VXQBJTKSVGFQOL-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl acetate Chemical compound CCCCOCCOCCOC(C)=O VXQBJTKSVGFQOL-UHFFFAOYSA-N 0.000 description 1
BJINVQNEBGOMCR-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl acetate Chemical compound COCCOCCOC(C)=O BJINVQNEBGOMCR-UHFFFAOYSA-N 0.000 description 1
DJCYDDALXPHSHR-UHFFFAOYSA-N 2-(2-propoxyethoxy)ethanol Chemical compound CCCOCCOCCO DJCYDDALXPHSHR-UHFFFAOYSA-N 0.000 description 1
GWQAFGZJIHVLGX-UHFFFAOYSA-N 2-(2-propoxyethoxy)ethyl acetate Chemical compound CCCOCCOCCOC(C)=O GWQAFGZJIHVLGX-UHFFFAOYSA-N 0.000 description 1
PTTPXKJBFFKCEK-UHFFFAOYSA-N 2-Methyl-4-heptanone Chemical compound CC(C)CC(=O)CC(C)C PTTPXKJBFFKCEK-UHFFFAOYSA-N 0.000 description 1
CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical compound CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
OMSLSFZIEVFEIH-UHFFFAOYSA-N 4-methoxy-4-methylpentan-2-ol Chemical compound COC(C)(C)CC(C)O OMSLSFZIEVFEIH-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
229920000896 Ethulose Polymers 0.000 description 1
239000001859 Ethyl hydroxyethyl cellulose Substances 0.000 description 1
101000687448 Homo sapiens REST corepressor 1 Proteins 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
235000019482 Palm oil Nutrition 0.000 description 1
102100024864 REST corepressor 1 Human genes 0.000 description 1
244000007853 Sarothamnus scoparius Species 0.000 description 1
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
230000009471 action Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
229940072049 amyl acetate Drugs 0.000 description 1
PGMYKACGEOXYJE-UHFFFAOYSA-N anhydrous amyl acetate Natural products CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
239000010425 asbestos Substances 0.000 description 1
239000010426 asphalt Substances 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
239000011449 brick Substances 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
229960000541 cetyl alcohol Drugs 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000003240 coconut oil Substances 0.000 description 1
235000019864 coconut oil Nutrition 0.000 description 1
239000006103 coloring component Substances 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
235000019326 ethyl hydroxyethyl cellulose Nutrition 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
125000005313 fatty acid group Chemical group 0.000 description 1
125000004991 fluoroalkenyl group Chemical group 0.000 description 1
125000003709 fluoroalkyl group Chemical group 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
MNWFXJYAOYHMED-UHFFFAOYSA-M heptanoate Chemical compound CCCCCCC([O-])=O MNWFXJYAOYHMED-UHFFFAOYSA-M 0.000 description 1
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
229920013821 hydroxy alkyl cellulose Polymers 0.000 description 1
229910010272 inorganic material Inorganic materials 0.000 description 1
239000011147 inorganic material Substances 0.000 description 1
229910052809 inorganic oxide Inorganic materials 0.000 description 1
GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 1
FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropanol acetate Natural products CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 1
239000004922 lacquer Substances 0.000 description 1
239000004571 lime Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
SHOJXDKTYKFBRD-UHFFFAOYSA-N mesityl oxide Natural products CC(C)=CC(C)=O SHOJXDKTYKFBRD-UHFFFAOYSA-N 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
230000004048 modification Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
125000005702 oxyalkylene group Chemical group 0.000 description 1
125000006353 oxyethylene group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000000049 pigment Substances 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229910052895 riebeckite Inorganic materials 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
229910052710 silicon Inorganic materials 0.000 description 1
239000010703 silicon Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000010959 steel Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
239000003760 tallow Substances 0.000 description 1
239000011269 tar Substances 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
239000002966 varnish Substances 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/222—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
- C11D3/225—Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin etherified, e.g. CMC
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D9/00—Chemical paint or ink removers
- C09D9/005—Chemical paint or ink removers containing organic solvents
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—Solvents

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Wood Science & Technology (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Emergency Medicine (AREA)
General Chemical & Material Sciences (AREA)
Materials Engineering (AREA)
Paints Or Removers (AREA)

NO743987A 1973-11-05 1974-11-05 NO743987L (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB51282/73A GB1487737A (en)	1973-11-05	1973-11-05	Paint removers
GB3209674		1974-07-19
GB3209774		1974-07-19

Publications (1)

Publication Number	Publication Date
NO743987L true NO743987L (fr)	1975-06-02

Family

ID=27259026

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO743987A NO743987L (fr)	1973-11-05	1974-11-05

Country Status (11)

Country	Link
JP (1)	JPS5079529A (fr)
BE (1)	BE821886A (fr)
DE (1)	DE2452443A1 (fr)
DK (1)	DK576574A (fr)
FI (1)	FI323074A7 (fr)
FR (1)	FR2249933B1 (fr)
GB (1)	GB1487737A (fr)
IE (1)	IE40851B1 (fr)
NL (1)	NL7414418A (fr)
NO (1)	NO743987L (fr)
SE (1)	SE7413876L (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5636555A (en) *	1979-08-31	1981-04-09	Tonbo Enpitsu:Kk	Composition for eraser
DE3170704D1 (en) *	1980-07-19	1985-07-04	Hubdean Ltd	Anti-graffiti facing of walls or similar surfaces
EP0065381A3 (fr) *	1981-05-08	1983-02-02	Norman Hodgson Shuttleworth	Agents décapants
JPS59470A (ja) *	1982-05-24	1984-01-05	日星産業株式会社	建造物における老化塗層の剥離除去方法
JPS5918856A (ja) *	1982-07-23	1984-01-31	日星産業株式会社	建造物における老化塗層の剥離除去方法
DE4003700A1 (de) *	1989-07-11	1991-01-24	Scheidel Georg Gmbh	Zubereitung zum loesen von beschichtungen und klebern
US6368421B1 (en) *	1998-07-10	2002-04-09	Clariant Finance (Bvi) Limited	Composition for stripping photoresist and organic materials from substrate surfaces
KR101207501B1 (ko)	2012-05-23	2012-12-03	(주)삼일폴리머	페인트 박리제 조성물 및 페인트 박리제
FR3027310B1 (fr)	2014-10-15	2017-12-15	Commissariat Energie Atomique	Gel pour eliminer les graffitis et procede pour eliminer les graffitis utilisant ce gel.
CN105542550B (zh) *	2015-12-31	2018-06-29	长沙艾森设备维护技术有限公司	一种环保型金属表面浮漆清洗剂
FR3057879B1 (fr)	2016-10-20	2020-03-27	Cecile Franc	Gel aqueux neutre et procede de traitement de surface le mettant en œuvre

1973
- 1973-11-05 GB GB51282/73A patent/GB1487737A/en not_active Expired
1974
- 1974-11-05 NL NL7414418A patent/NL7414418A/xx not_active Application Discontinuation
- 1974-11-05 NO NO743987A patent/NO743987L/no unknown
- 1974-11-05 BE BE150240A patent/BE821886A/fr unknown
- 1974-11-05 FI FI3230/74A patent/FI323074A7/fi unknown
- 1974-11-05 SE SE7413876A patent/SE7413876L/xx unknown
- 1974-11-05 DE DE19742452443 patent/DE2452443A1/de active Pending
- 1974-11-05 FR FR7436752A patent/FR2249933B1/fr not_active Expired
- 1974-11-05 IE IE2270/74A patent/IE40851B1/xx unknown
- 1974-11-05 JP JP49127926A patent/JPS5079529A/ja active Pending
- 1974-11-05 DK DK576574A patent/DK576574A/da not_active Application Discontinuation

Also Published As

Publication number	Publication date
DE2452443A1 (de)	1975-05-15
FI323074A7 (fr)	1975-05-06
FR2249933A1 (fr)	1975-05-30
IE40851B1 (en)	1979-08-29
JPS5079529A (fr)	1975-06-28
BE821886A (fr)	1975-03-03
NL7414418A (nl)	1975-05-07
GB1487737A (en)	1977-10-05
IE40851L (en)	1975-05-05
FR2249933B1 (fr)	1978-09-15
SE7413876L (fr)	1975-05-06
DK576574A (fr)	1975-07-07

Publication	Publication Date	Title
CA1321534C (fr)	1993-08-24	Composes decapants hydrosolubles
US6489272B2 (en)	2002-12-03	Lubricant, solvent and emulsifier composition and method of manufacture
US5049300A (en)	1991-09-17	Method of activating acidified NMP to provide an effective paint remover composition
CA2172148C (fr)	1999-04-20	Compositions d'emulsions biodegradables non toxiques destinees aux installations de lavage automatique de voitures
US5035829A (en)	1991-07-30	Paint removing compositions
EP0435943A1 (fr)	1991-07-10	UTILISATION D'ESTERS D'ALKYLE (C-1 à C-5) D'ACIDES MONOCARBOXYLIQUES (C-8 à C-22) ALIPHATIQUES POUR L'ENLEVEMENT DES ENCRES ET AUTRES SUBSTANCES SIMILAIRES DE MACHINES A IMPRIMER.
EP0551378A1 (fr)	1993-07-21	Procede d'activation de solvants n-methyl-2-pyrrolidone (nmp) et/ou gamma-butyrolactone (blo) utilise pour oter le vernis et la peinture
US2335882A (en)	1943-12-07	Printing ink
IL181704A (en)	2012-01-31	Aqueous fixer fluid for printing before or after an aqueous inkjet ink and method for using same
DE2452443A1 (de)	1975-05-15	Farbentfernmasse auf der basis organischer loesungsmittel
GB2191501A (en)	1987-12-16	Graffiti removal composition
EP0065381A2 (fr)	1982-11-24	Agents décapants
US5154848A (en)	1992-10-13	Method of activating N-methyl-2-pyrrolidone (NMP) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US11220609B2 (en)	2022-01-11	Natural oil based cleaners
CN106947635B (zh)	2018-07-06	洗车液及其制备方法、以及洗车方法
JP2002327397A (ja)	2002-11-15	紙用透明化剤
JPH08218027A (ja)	1996-08-27	油性インキ組成物
CN114805467B (zh)	2023-06-23	一种在酸性和高脂肪性油污下具有强起泡能力的茶皂素双子表面活性剂
SU1117313A1 (ru)	1984-10-07	Моющее средство дл очистки прецизионных деталей от минеральных масел и жиров
US2047889A (en)	1936-07-14	Baking enamel
SU1730113A1 (ru)	1992-04-30	Водно-эмульсионный крем дл обуви
US2090630A (en)	1937-08-24	Casein solution
US2302286A (en)	1942-11-17	Filler composition
CN104685046B (zh)	2018-05-22	二乙酰丙酸二醇酯作为清洗制剂中的偶联剂
JPS644550B2 (fr)	1989-01-26