EP0113917B1 - Method and compositions for removal of undesirable organic matter - Google Patents
Method and compositions for removal of undesirable organic matter Download PDFInfo
- Publication number
- EP0113917B1 EP0113917B1 EP83113169A EP83113169A EP0113917B1 EP 0113917 B1 EP0113917 B1 EP 0113917B1 EP 83113169 A EP83113169 A EP 83113169A EP 83113169 A EP83113169 A EP 83113169A EP 0113917 B1 EP0113917 B1 EP 0113917B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- imidazole
- organic matter
- pyrazole
- alkyl
- aryl substituted
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 81
- 239000005416 organic matter Substances 0.000 title claims abstract description 23
- 238000000034 method Methods 0.000 title claims abstract description 14
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims abstract description 113
- 239000002689 soil Substances 0.000 claims abstract description 32
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 150000002460 imidazoles Chemical class 0.000 claims abstract description 18
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 125000003118 aryl group Chemical group 0.000 claims abstract description 10
- 235000013305 food Nutrition 0.000 claims abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- -1 aryl substituted pyrazole Chemical compound 0.000 claims description 12
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 10
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 8
- 235000002639 sodium chloride Nutrition 0.000 claims description 7
- 239000002562 thickening agent Substances 0.000 claims description 7
- 239000002585 base Substances 0.000 claims description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 5
- 239000003518 caustics Substances 0.000 claims description 5
- 239000007788 liquid Substances 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- XLSZMDLNRCVEIJ-UHFFFAOYSA-N 4-methylimidazole Chemical compound CC1=CNC=N1 XLSZMDLNRCVEIJ-UHFFFAOYSA-N 0.000 claims description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229920002125 Sokalan® Polymers 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 239000006185 dispersion Substances 0.000 claims description 3
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 claims description 3
- 229910052939 potassium sulfate Inorganic materials 0.000 claims description 3
- 235000011151 potassium sulphates Nutrition 0.000 claims description 3
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 claims description 2
- PQAMFDRRWURCFQ-UHFFFAOYSA-N 2-ethyl-1h-imidazole Chemical compound CCC1=NC=CN1 PQAMFDRRWURCFQ-UHFFFAOYSA-N 0.000 claims description 2
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 claims description 2
- ULKLGIFJWFIQFF-UHFFFAOYSA-N 5K8XI641G3 Chemical compound CCC1=NC=C(C)N1 ULKLGIFJWFIQFF-UHFFFAOYSA-N 0.000 claims description 2
- 229920003091 Methocel™ Polymers 0.000 claims description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 claims description 2
- 239000001768 carboxy methyl cellulose Substances 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 239000010433 feldspar Substances 0.000 claims description 2
- 229910010272 inorganic material Inorganic materials 0.000 claims description 2
- 239000011147 inorganic material Substances 0.000 claims description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 2
- 239000001095 magnesium carbonate Substances 0.000 claims description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 2
- 239000000347 magnesium hydroxide Substances 0.000 claims description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 2
- 239000001103 potassium chloride Substances 0.000 claims description 2
- 235000011164 potassium chloride Nutrition 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 claims description 2
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 claims description 2
- 239000011780 sodium chloride Substances 0.000 claims description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 claims description 2
- 235000011152 sodium sulphate Nutrition 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- 229920001285 xanthan gum Polymers 0.000 claims description 2
- IPIORGCOGQZEHO-UHFFFAOYSA-N 1-propan-2-ylimidazole Chemical compound CC(C)N1C=CN=C1 IPIORGCOGQZEHO-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- 229910000323 aluminium silicate Inorganic materials 0.000 claims 1
- 235000012211 aluminium silicate Nutrition 0.000 claims 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 claims 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 239000000230 xanthan gum Substances 0.000 claims 1
- 229940082509 xanthan gum Drugs 0.000 claims 1
- 235000010493 xanthan gum Nutrition 0.000 claims 1
- 239000003973 paint Substances 0.000 abstract description 6
- 239000004480 active ingredient Substances 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 description 22
- 238000004140 cleaning Methods 0.000 description 16
- 238000000576 coating method Methods 0.000 description 11
- 239000000463 material Substances 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000001680 brushing effect Effects 0.000 description 5
- 239000003925 fat Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- NOIXNOMHHWGUTG-UHFFFAOYSA-N 2-[[4-[4-pyridin-4-yl-1-(2,2,2-trifluoroethyl)pyrazol-3-yl]phenoxy]methyl]quinoline Chemical class C=1C=C(OCC=2N=C3C=CC=CC3=CC=2)C=CC=1C1=NN(CC(F)(F)F)C=C1C1=CC=NC=C1 NOIXNOMHHWGUTG-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 229910052573 porcelain Inorganic materials 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
- 239000010935 stainless steel Substances 0.000 description 4
- XKVUYEYANWFIJX-UHFFFAOYSA-N 5-methyl-1h-pyrazole Chemical compound CC1=CC=NN1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 description 3
- 241000287828 Gallus gallus Species 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- 239000000344 soap Substances 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 2-phenyl-1h-imidazole Chemical compound C1=CNC(C=2C=CC=CC=2)=N1 ZCUJYXPAKHMBAZ-UHFFFAOYSA-N 0.000 description 2
- XHLKOHSAWQPOFO-UHFFFAOYSA-N 5-phenyl-1h-imidazole Chemical compound N1C=NC=C1C1=CC=CC=C1 XHLKOHSAWQPOFO-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 150000001339 alkali metal compounds Chemical class 0.000 description 2
- 239000008365 aqueous carrier Substances 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- MCTWTZJPVLRJOU-UHFFFAOYSA-N 1-methyl-1H-imidazole Chemical compound CN1C=CN=C1 MCTWTZJPVLRJOU-UHFFFAOYSA-N 0.000 description 1
- FUOZJYASZOSONT-UHFFFAOYSA-N 2-propan-2-yl-1h-imidazole Chemical compound CC(C)C1=NC=CN1 FUOZJYASZOSONT-UHFFFAOYSA-N 0.000 description 1
- SDXAWLJRERMRKF-UHFFFAOYSA-N 3,5-dimethyl-1h-pyrazole Chemical compound CC=1C=C(C)NN=1 SDXAWLJRERMRKF-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 240000003183 Manihot esculenta Species 0.000 description 1
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000021168 barbecue Nutrition 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- UREZNYTWGJKWBI-UHFFFAOYSA-M benzethonium chloride Chemical compound [Cl-].C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 UREZNYTWGJKWBI-UHFFFAOYSA-M 0.000 description 1
- OYVWCXTZVTZQFZ-UHFFFAOYSA-M benzyl-(2-ethoxyethyl)-dimethylazanium;chloride;hydrate Chemical compound O.[Cl-].CCOCC[N+](C)(C)CC1=CC=CC=C1 OYVWCXTZVTZQFZ-UHFFFAOYSA-M 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 235000013351 cheese Nutrition 0.000 description 1
- 235000015120 cherry juice Nutrition 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000012041 food component Nutrition 0.000 description 1
- 239000005417 food ingredient Substances 0.000 description 1
- 150000004820 halides Chemical group 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003791 organic solvent mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- DUXXGJTXFHUORE-UHFFFAOYSA-M sodium;4-tridecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 DUXXGJTXFHUORE-UHFFFAOYSA-M 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 235000015193 tomato juice Nutrition 0.000 description 1
- 239000002966 varnish Substances 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
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 230000037303 wrinkles Effects 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
- C11D3/26—Organic compounds containing nitrogen
- C11D3/28—Heterocyclic compounds containing nitrogen in the ring
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0057—Oven-cleaning compositions
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/32—Organic compounds containing nitrogen
- C11D7/3281—Heterocyclic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- General Preparation And Processing Of Foods (AREA)
- Processing Of Solid Wastes (AREA)
- Soil Conditioners And Soil-Stabilizing Materials (AREA)
Abstract
Description
- The removal of undesirable organic matter from various hard surfaces such as metal, ceramics, baked enamel has received a great deal of study. The organic matter referred to herein occurs for example, as soil in ovens, on baking pans and barbecue racks, as finishes, coatings, paints and the like.
- Oven soil which contains baked-on fat and other food ingredients is usually cleaned by applying to the soil thickened solutions of one of the caustic metal alkalis, either sodium or potassium hydroxide. These materials react with and hydrolyze the fats, converting them at least partially into their sodium or potassium salts, which are water soluble. These water soluble soaps are then washed out of the oven with a wet rag or sponge. Commercial products of this type usually contain up to 5% of the metal hydroxide together with other components such as solvents, wetting agents, etc., which contribute to the efficacy of the product.
- Products of the type described, although efficient in their cleaning ability, suffer a number of major disadvantages. They are corrosive and, hence, are severely hazardous to the eyes and skin. Also, the residue after cleaning is slimy due to the saponification reaction and unreacted cleaner, making the task of removing the residue both messy and burdensome.
- Non-caustic compositions for removal of oven soil are described in U.S. Patent Nos. 4,236,935; 4,193,886; 4,116,848; and 3,808,051. However, all appear to describe a saponification reaction with the formation of water soluble or dispersible soaps. The residue from the reaction would be washed out with a wet or damp sponge. Heating the composition on the soil to a temperature of at least 250°F. is also necessary for cleaning to occur.
- U.S. Patent 3,881,948 also describes a non-caustic composition, based on a polyhydric alcohol and an alkaline acting catalyst. Here the reaction also forms water soluble or water dispersible compounds which must be washed out of the oven. Heating the composition on the soil to a temperature of at least 250°F. is necessary for cleaning to occur.
- For the removal of finishes, coatings, paints, and the like, aqueous solutions of alkali metal hydroxides have been used to saponify the fatty acid constituents of the bonding component of the composition, thereby loosening and facilitating the removal thereof. Such products have similar disadvantages to the oven cleaner compositions based on alkali metal hydroxides in that they are corrosive to the eye and skin. These "stripping" compositions generally contain other additives such as water miscible solvents, accelerators, surfactants and thickeners, to aid product performance. For example, U.S. Patent No. 3,819,529 discloses a paint stripping composition consisting.essentially of an inorganic alkaline material selected from the group consisting of alkali metal hydroxides, carbonates, silicates, and phosphates and an alkyl or aryl (having not more than six (6) carbon atoms) substituted imidazole. The substituted imidazole is described as an accelerator. Although the disclosure of this patent is confusing as to necessary components which comprise the stripping composition, it is clear that the substituted imidazole is not the stripping agent, but only acts to increase the rate of attack. It is the strong alkali metal compounds which operate to loosen the paint from the surface.
- It is, accordingly, an object of the invention to provide a novel method and novel compositions for the removal of organic matter from surfaces.
- It is a further object of the invention to provide novel compositions which are non-caustic, non-corrosive, and essentially non-irritating to the eyes and skin.
- It is another object of the invention to provide a novel method and novel compositions which give a relatively dry residue which may be physically removed from the surface by wiping or brushing.
- It is yet another object of the invention to provide such novel compositions which are useful in a variety of forms, such as paste, aerosol, and pump spray.
- These and other objects and advantages of the instant invention will become apparent from the following detailed description.
- The novel method of the invention comprises contacting the undesirable organic matter with a substantially loosening effective amount of a compound selected from imidazole, pyrazole, an alkyl or aryl substituted imidazole, an alkyl or aryl substituted pyrazole, or a mixture of two or more thereof in liquid form in the substantial absence of an alkali metal hydroxide for a time sufficient to effect a substantial loosening of said organic matter.
- Compositions containing the imidazole, pyrazole, substituted imidazole or substituted pyrazole as the active ingredient together with a carrier and a thickening agent and in the substantial absence of an alkali metal hydroxide are also within the scope of the invention.
- Obviously, two or more of these compounds may be used in combination in the method or compositions of the present invention. Compounds falling within the scope of an alkyl or aryl substituted imidazole include, inter alia, 1-methylimidazole, 2-methylimidazole, 4-methylimidazole, 1,2-dimethylimidazole, 2-ethylimidazole, 2-isopropylimidazole, 2-ethyl-4-methylimidazole, 2-phenylimidazole, 4-phenylimidazole, benzimidazole and the like. Compounds falling within the scope of an alkyl or aryl substituted pyrazole include 3-methylpyrazole, 3,5-dimethylpyrazole and the like.
- The imidazole, pyrazole, alkyl or aryl substituted imidazole, or alkyl or aryl substituted pyrazole is effective by itself, without the need for a carrier, or additional ingredients, such as the alkali metal compounds required in U.S. Patent No. 3,819,529, supra, provided only that the compound be in liquid form at use temperature.
- Obviously, it is also desirable that the imidazole, pyrazole, substituted imidazole or substituted pyrazole be maintained in contact with the soiled substrate to effectuate maximum cleaning. Accordingly, thickened solutions or suspensions of the compound which may be applied as a paste or via pump spray or aerosol systems would be preferred for many applications, such as in oven cleaning, where the compound must be maintained on an overhead and/or vertical surface. Preparation of these aerosol, pump spray and paste compositions are within the ordinary skill in the art.
- When used with a carrier (or carrier plus additional ingredients), the concentration of the imidazole, pyrazole, substituted imidazole or substituted pyrazole may vary over a wide range-from as little as about 1%, by weight, to as much as about 99%, by weight. Preferably, the imidazole, pyrazole, substituted imidazole or substituted pyrazole will comprise about 5 to 25% by weight, of the total composition. Aqueous carriers, or water and water miscible organic solvent mixtures are preferred. It.has been found that the aryl substituted and higher alkyl (chain length greater than two (2) carbons) substituted imidazoles and pyrazoles are not very soluble in water and, accordingly, the use of a co-solvent in a composition containing any of these compounds and water may be desirable. Alternatively, a non-aqueous carrier may be used. When the particular compound used is not liquid at a desired use temperature (such as room temperature), these carriers may be used to solubilize the compound, and accordingly the carrier system may be routinely chosen by one skilled in the art taking into consideration the solubility of the particular compound being used in various solvent mixtures, and the intended use. Alternatively, of course, the compound may be applied as a dispersion thereof in a carrier, or in a dry state at, for example, room temperature and the system heated to a temperature sufficient to cause the compound to be solubilized in the carrier or melt, thereby rendering the same "active".
- When a thickening agent is desirably used with the compound, for example when the organic matter to be removed is on a non-horizontal surface, any such agent, or mixture of two or more thereof, which is compatible with the imidazole, pyrazole or substituted imidazole or pyrazole (and with other ingredients in a formulation, if a formulation is used) may be used. Useful organic thickening agents include starch, sodium carboxymethylcellulose, hydroxyethyl cellulose, methocel, and water-soluble polymers such as carboxy vinyl polymer (Carbopols from B. F. Goodrich Chemical Company) and most preferred are Xanthan gums such as Keltrol@, made by Kelco Company. Inorganic colloidal materials, such as Veegum (magnesium aluminum silicates manufactured by R. T. Vanderbilt), are also effective. When used, the thickening agent will typically comprise about 0.1 to 10%, by weight, of the composition, although more or less may be used.
- It may also be preferable in certain instances to have present as a component of the composition of the present invention a minor amount of surface active agent which will cause the composition to spread evenly over the surface from which the undesirable organic matter is to be removed, or to form a foam. The surface active agents can be any of those commonly known and used as such. An extensive list of such agents appears in the publication McCutcheon's Detergents & Emulsifiers, 1982 Annual. The agents can be anionic, cationic, nonionic, or amphoteric and should be compatible with the other ingredients and impart the desired surface active properties. When used, the surface active agent will typically comprise about 0.01 to 0.8%, by weight, of the composition, although more or less may be used.
- Examples of anionic surfactants include (a) carboxylic acids such as soaps of straight chain naturally occurring fatty acids, chain-substituted derivatives of fatty acids, branched-chain and odd-carbon fatty acids, acids from paraffin oxidation, and carboxylic acids with intermediate linkages; (b) sulfuric esters such as sodium lauryl sulfate, tallow alcohol sulfates and coconut alcohol sulfates; and (c) alkylaryl sulfonates such as sodium dodecylbenzene sulfonate, sodium tridecyl benzene sulfonate, and sodium dodecyl diphenyloxide disulphonate.
- Examples of cationic surfactants include (a) non-quaternary nitrogen bases such as amines without intermediate linkages; and (b) quaternary nitrogen bases of the formula:
- Examples of nonionic surfactants include polyethylenoxy ethers of alkylphenols, alkanols, esters and polyethylenoxy compounds with amide links.
- In one embodiment of the composition of the invention, a water insoluble, finely divided material is suspended therein to aid in removing the organic matter and residual composition after the organic matter has been loosened from the surface. Although the addition of these materials assist in the removal of varnish, finishes, coatings, paints, and the like, it has been found to be particularly beneficial for the removal of oven soil. In oven cleaning applications, the addition of these materials has been found to contribute to the ease of removal of the organic matter (and residual composition) from the oven surface after the cleaning cycle by wiping with a dry paper towel, a brush or the like. When used, the amount of such finely divided material present in the composition of the present invention typically ranges from about 1 to 25%, by weight, of the composition, preferably about 2 to 10%, although more or less may be used. Examples of such finely divided inorganic material include calcium carbonate, magnesium carbonate, magnesium hydroxide, silica, feldspar, clay and talc.
- In another embodiment of the composition of the present invention, a water soluble salt of a strong base and a strong acid is added to the composition containing the imidazole, pyrazole, or substituted imidazole or pyrazole, the carrier and the thickening agent. The addition of the salt has been found to improve the soil loosening activity of the composition and also contributes to the ease of removal of the organic matter and residual composition. Here again, the benefit has been found to be particularly pronounced in oven cleaning applications. When used, the amount of the salt typically ranges from about 1% to 25% by weight, of the composition depending, of course, upon the solubility of the compound being used, and is preferably about 1% to 10%, by weight, of the composition, although more or less may be used. Examples of such water soluble salts include sodium chloride, potassium chloride, sodium sulfate, and potassium sulfate.
- Other additives which are typically used in compositions for removal of organic matter may also be used in the compositions of the present invention, provided, of course, that they are compatible therewith. Exemplary of such other additives are humectants, anti-foaming agents, dispersants and the like.
- It is an advantage of the method and compositions of the present invention that the same may be employed at room temperature, or at elevated temperatures when speedier cleaning is desired or necessary, such as in oven cleaning applications.
-
-
- The present invention is further illustrated by the following examples. However, it is to be understood that the invention is not to be deemed in any way limited by these examples. All parts and percentages are by weight unless indicated to the contrary.
- A fifty percent chicken fat, fifty percent lard soil composition was baked on a stainless steel plate at 260°C (500°F). for 30 minutes. The baking converted the chicken fat and lard into a hard, brown, varnish-like coating, similar in composition and appearance to the fatty soil found in ovens. After cooling, imidazole was applied to the soil, and the plate heated to 148.9°C (300°F). for 60 minutes. The imidazole melted on the soil. During the heating cycle, it was observed that the soil wrinkled and broke away from the metal surface. Upon cooling, the imidazole resolidified with the wrinkled soil, and the residue was readily brushed from the metal surface.
- A forty percent solution of imidazole in water was applied to a stainless steel plate having the baked-on soil composition of Example 1 thereon, and heated to 148.9°C (300°F). for one hour. Results were similar to those achieved in Example 1.
- Twenty-five and ten percent solutions of imidazole in water were each separately applied to stainless steel plates having the baked-on soil of Example 1 thereon, and heated to 107.2°C (225°F), 190.6°C (375°F), and 273.9°C (525°F). for 60 minutes. Best loosening of the soil occurred at 107.2°C (225°F). for both solutions, it being theorized that at the higher temperatures some of the imidazole was lost due to evaporation, thereby reducing the cleaning efficacy thereof.
-
- The formulations were applied to soiled stainless steel plates having the baked-on soil composition of Example 1 thereon, and heated for one hour at 107.2°C (225°F)., 130.6°C (375°F)., and 273.9°C (525°F). As in Examples 3 and 4, best loosening of the soil occurred at 107.2°C (225°F). At this temperature, both formulations gave excellent removal of the soil. The ease of removal of the residue by physical means such as wiping with sponge, paper towel, scrubbing pad, etc., or by brushing was improved as compared to formulations not containing calcium carbonate.
- A fifty percent chicken fat, fifty percent lard soil composition was baked onto six (6) porcelain enameled test trays at 260°C (500°F). for 30 minutes.
-
- Each of the formulations was applied (30 g/1000 cm2) to three (3) of the soiled trays as follows:
- Condition A: Applied at ambient temperature (about 20 to 25°C (68 to 77°F)). and left for sixteen (16) hours without heat, in a household oven;
- Condition B: Applied at ambient temperature, then heated in oven at 107.2°C (225°F). for fifteen (15) minutes, then allowed to cool;
- Condition C: Applied to warm 93.3°C (200°F) soiled tray, then allowed to cool gradually in oven.
- Very good (at least 90%) soil removal was obtained with the formulation containing ten (10) percent imidazole at all three cleaning conditions. The formulation residue could also be easily removed from the surface by brushing. Good (60 to 90%) removal was obtained with the formulation containing five (5) percent imidazole. Ease of removal of the residue was also good.
-
- The formulations were applied to soiled porcelain enameled test trays, prepared as described in Examples 7 and 8, and evaluated using the three (3) test condition described in Examples 7 and 8 for both soil removal and ease of removing the residue by brushing.
- Very good soil removal and ease of residue removal was obtained with the formulation containing the calcium carbonate. However, even better soil removal was obtained with the formulation containing the potassium sulfate and calcium carbonate. The ease of brushing the residue off the tray was also improved. These test results were obtained at all three test conditions.
-
- There was then added to this base formulation varying amounts of imidazole and substituted imidazoles as shown in Table 1, and water to total one hundred (100) percent.
- The various formulations were applied (30 g/1000 cm2) to soiled porcelain enameled test trays, prepared as described in Examples 7 and 8, and evaluated using the three test conditions described in Examples 7 and 8.
- At the end of each treatment, the soil plus the residual formulation was brushed from each treated plate followed by wiping with a damp sponge. The overall degree of cleaning was evaluated according to the following scale:
- VG-Very good-at least 90% of treated area cleaned.
- GGood6090% of treated area cleaned.
- F-Fair-25-60% of treated area cleaned.
- P-Poor-some cleaning occurred, but less than 25% of treated area cleaned.
- A soil composition containing 120 g. ground beef, 58 g. cheddar cheese, 120 ml. milk, 110 g. sugar, 120 ml. cherry juice, 19 g. tapioca, 1 egg, 15 g. flour and 120 ml. tomato juice was prepared by mixing with a hand mixer (low speed) for 3 minutes. The soil was baked onto a porcelain enameled test tray at 232°C (450°F). for 60 minutes. After cooling, imidazole was applied to the soil, and the plate heated to 149°C (300°F). for 60 minutes. The results obtained were similar to those achieved in Example 1.
- The procedure of Example 1 is repeated, except that 2-phenylimidazole, 4-phenylimidazole, benzimidazole, pyrazole and 3-methylpyrazole are each separately substituted for imidazole. At least fair (25-60%) soil removal is accomplished in each instance.
-
- Both formulations were tested for their ability to remove a variety of organic coatings from surfaces as follows:
- The following twelve (12) coatings were each brushed or sprayed on one (1) wood and one (1) metal surface test panel according to label directions. The twenty-four (24) test panels were then dried overnight, and aged for eight (8) hours at 100°C. in an air circulation oven.
- To 25 cm2 of each of the so prepared test panels was then uniformly applied about 5 grams of each formulation, above, at room temperature (about 21°C.).
- For coatings 1 through 10, wrinkles began appearing in the tested areas after about 1 hour. The entire treated area wrinkled within about 4 hours, and the treated area was easily wiped clean.
- For coating 11, bubbles developed in the treated area, and about 25% of the treated area was brushed clean.
- For coating 12, after two (2) hours, all polish on the treated area was easily removed by washing with water.
- The procedure of Examples 18 and 19 is repeated, except that 3-methylpyrazole and pyrazole are separately substituted for the imidazole. Substantial removal of the twelve (12) coatings from both wood and metal surface test panels is accomplished.
Claims (8)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT83113169T ATE26310T1 (en) | 1983-01-17 | 1983-12-28 | METHODS AND COMPOSITIONS FOR REMOVAL OF UNWANTED ORGANIC MATERIAL. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US45822983A | 1983-01-17 | 1983-01-17 | |
US458229 | 1983-01-17 |
Publications (2)
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EP0113917A1 EP0113917A1 (en) | 1984-07-25 |
EP0113917B1 true EP0113917B1 (en) | 1987-04-01 |
Family
ID=23819899
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP83113169A Expired EP0113917B1 (en) | 1983-01-17 | 1983-12-28 | Method and compositions for removal of undesirable organic matter |
Country Status (9)
Country | Link |
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EP (1) | EP0113917B1 (en) |
AT (1) | ATE26310T1 (en) |
AU (1) | AU563973B2 (en) |
BR (1) | BR8400175A (en) |
CA (1) | CA1227393A (en) |
DE (1) | DE3370656D1 (en) |
MX (1) | MX161332A (en) |
NZ (1) | NZ206796A (en) |
ZA (1) | ZA84330B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US5137793A (en) * | 1990-08-01 | 1992-08-11 | Kay Chemical Company | Cooking equipment pretreatment composition and method of use |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3819529A (en) * | 1973-01-17 | 1974-06-25 | Oxy Metal Finishing Corp | Imidazole stripping composition and method |
US4214915A (en) * | 1978-08-07 | 1980-07-29 | Colgate-Palmolive Company | Method and composition for cleaning ovens |
-
1983
- 1983-12-28 EP EP83113169A patent/EP0113917B1/en not_active Expired
- 1983-12-28 DE DE8383113169T patent/DE3370656D1/en not_active Expired
- 1983-12-28 AT AT83113169T patent/ATE26310T1/en not_active IP Right Cessation
-
1984
- 1984-01-10 NZ NZ206796A patent/NZ206796A/en unknown
- 1984-01-13 CA CA000445293A patent/CA1227393A/en not_active Expired
- 1984-01-16 ZA ZA84330A patent/ZA84330B/en unknown
- 1984-01-16 AU AU23289/84A patent/AU563973B2/en not_active Expired
- 1984-01-16 BR BR8400175A patent/BR8400175A/en not_active IP Right Cessation
- 1984-01-17 MX MX200063A patent/MX161332A/en unknown
Non-Patent Citations (1)
Title |
---|
PATENTS ABSTRACTS OF JAPAN, unexamined applications, C Section, Vol. 1, No. 28, March 28, 1977 THE PATENT OFFICE JAPANESE GOVERNMENT page 1403 C 76 * |
Also Published As
Publication number | Publication date |
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CA1227393A (en) | 1987-09-29 |
BR8400175A (en) | 1984-08-21 |
AU2328984A (en) | 1984-07-19 |
ZA84330B (en) | 1984-08-29 |
DE3370656D1 (en) | 1987-05-07 |
ATE26310T1 (en) | 1987-04-15 |
AU563973B2 (en) | 1987-07-30 |
EP0113917A1 (en) | 1984-07-25 |
NZ206796A (en) | 1987-02-20 |
MX161332A (en) | 1990-09-10 |
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