NO333717B1 - Anti-fryskonsentrat inneholdende fargestoffet C.I. Reactive Violet 5, fremstilling og anvendelse derav, og vandig klar-til-bruk-kjolemiddelpreparat omfattende slikt konsentrat - Google Patents
Anti-fryskonsentrat inneholdende fargestoffet C.I. Reactive Violet 5, fremstilling og anvendelse derav, og vandig klar-til-bruk-kjolemiddelpreparat omfattende slikt konsentrat Download PDFInfo
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- NO333717B1 NO333717B1 NO20034959A NO20034959A NO333717B1 NO 333717 B1 NO333717 B1 NO 333717B1 NO 20034959 A NO20034959 A NO 20034959A NO 20034959 A NO20034959 A NO 20034959A NO 333717 B1 NO333717 B1 NO 333717B1
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- concentrate
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- freeze
- acid
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- 239000012141 concentrate Substances 0.000 title claims abstract description 66
- 230000002528 anti-freeze Effects 0.000 title claims abstract description 38
- 108010053481 Antifreeze Proteins Proteins 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims description 18
- 239000000203 mixture Substances 0.000 title claims description 13
- 239000003507 refrigerant Substances 0.000 title description 6
- DLPITEUCXDBWSF-UHFFFAOYSA-K trisodium N-[8-oxido-7-[[2-oxido-4-(2-sulfooxyethylsulfonyl)phenyl]diazenyl]-3,6-disulfonaphthalen-1-yl]ethanimidate Chemical compound CC(=NC1=C2C(=CC(=C1)S(=O)(=O)O)C=C(C(=C2[O-])N=NC3=C(C=C(C=C3)S(=O)(=O)CCOS(=O)(=O)O)[O-])S(=O)(=O)O)[O-].[Na+].[Na+].[Na+] DLPITEUCXDBWSF-UHFFFAOYSA-K 0.000 title 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 39
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 27
- 239000000975 dye Substances 0.000 claims description 24
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- 125000001931 aliphatic group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
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- 150000002391 heterocyclic compounds Chemical class 0.000 claims description 9
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- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
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- 125000003118 aryl group Chemical group 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
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- 125000002619 bicyclic group Chemical group 0.000 claims description 3
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- 229910001515 alkali metal fluoride Inorganic materials 0.000 claims description 2
- 229910001963 alkali metal nitrate Inorganic materials 0.000 claims description 2
- 229910000318 alkali metal phosphate Inorganic materials 0.000 claims description 2
- 229910001618 alkaline earth metal fluoride Inorganic materials 0.000 claims description 2
- 229910001964 alkaline earth metal nitrate Inorganic materials 0.000 claims description 2
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- 238000000034 method Methods 0.000 claims description 2
- 229910052605 nesosilicate Inorganic materials 0.000 claims description 2
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 claims description 2
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- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
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- 150000007513 acids Chemical class 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 4
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- 238000012360 testing method Methods 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- DZDVMKLYUKZMKK-UHFFFAOYSA-N 7-methyloctan-1-amine Chemical compound CC(C)CCCCCCN DZDVMKLYUKZMKK-UHFFFAOYSA-N 0.000 description 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 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 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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- FPAYXBWMYIMERV-UHFFFAOYSA-L disodium;5-methyl-2-[[4-(4-methyl-2-sulfonatoanilino)-9,10-dioxoanthracen-1-yl]amino]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1S([O-])(=O)=O FPAYXBWMYIMERV-UHFFFAOYSA-L 0.000 description 2
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- 125000001424 substituent group Chemical group 0.000 description 2
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- XUDJOVURIXHNRW-UHFFFAOYSA-N 1-amino-4-anilinoanthracene-9,10-dione Chemical group C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=CC=C1NC1=CC=CC=C1 XUDJOVURIXHNRW-UHFFFAOYSA-N 0.000 description 1
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- 239000004115 Sodium Silicate Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 229960000643 adenine Drugs 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- OYTKINVCDFNREN-UHFFFAOYSA-N amifampridine Chemical compound NC1=CC=NC=C1N OYTKINVCDFNREN-UHFFFAOYSA-N 0.000 description 1
- 229960004012 amifampridine Drugs 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 150000004699 copper complex Chemical class 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- LJOODBDWMQKMFB-UHFFFAOYSA-N cyclohexylacetic acid Chemical compound OC(=O)CC1CCCCC1 LJOODBDWMQKMFB-UHFFFAOYSA-N 0.000 description 1
- VWTINHYPRWEBQY-UHFFFAOYSA-N denatonium Chemical compound [O-]C(=O)C1=CC=CC=C1.C=1C=CC=CC=1C[N+](CC)(CC)CC(=O)NC1=C(C)C=CC=C1C VWTINHYPRWEBQY-UHFFFAOYSA-N 0.000 description 1
- 229960001610 denatonium benzoate Drugs 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 1
- 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 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019233 fast yellow AB Nutrition 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- GPSDUZXPYCFOSQ-UHFFFAOYSA-N m-toluic acid Chemical compound CC1=CC=CC(C(O)=O)=C1 GPSDUZXPYCFOSQ-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 1
- 239000011654 magnesium acetate Substances 0.000 description 1
- 235000011285 magnesium acetate Nutrition 0.000 description 1
- 229940069446 magnesium acetate Drugs 0.000 description 1
- CQQJGTPWCKCEOQ-UHFFFAOYSA-L magnesium dipropionate Chemical compound [Mg+2].CCC([O-])=O.CCC([O-])=O CQQJGTPWCKCEOQ-UHFFFAOYSA-L 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- KYWBVOVSUISYPN-UHFFFAOYSA-L magnesium;benzenesulfonate Chemical compound [Mg+2].[O-]S(=O)(=O)C1=CC=CC=C1.[O-]S(=O)(=O)C1=CC=CC=C1 KYWBVOVSUISYPN-UHFFFAOYSA-L 0.000 description 1
- YJWSPTRABMNCGQ-UHFFFAOYSA-L magnesium;methanesulfonate Chemical compound [Mg+2].CS([O-])(=O)=O.CS([O-])(=O)=O YJWSPTRABMNCGQ-UHFFFAOYSA-L 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- IJFXRHURBJZNAO-UHFFFAOYSA-N meta--hydroxybenzoic acid Natural products OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- LJXQPZWIHJMPQQ-UHFFFAOYSA-N pyrimidin-2-amine Chemical compound NC1=NC=CC=N1 LJXQPZWIHJMPQQ-UHFFFAOYSA-N 0.000 description 1
- HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical compound SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 235000019795 sodium metasilicate Nutrition 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- UQMOLLPKNHFRAC-UHFFFAOYSA-N tetrabutyl silicate Chemical compound CCCCO[Si](OCCCC)(OCCCC)OCCCC UQMOLLPKNHFRAC-UHFFFAOYSA-N 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- ZQZCOBSUOFHDEE-UHFFFAOYSA-N tetrapropyl silicate Chemical compound CCCO[Si](OCCC)(OCCC)OCCC ZQZCOBSUOFHDEE-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/20—Antifreeze additives therefor, e.g. for radiator liquids
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Combustion & Propulsion (AREA)
- Thermal Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thermotherapy And Cooling Therapy Devices (AREA)
- Medicinal Preparation (AREA)
- Detergent Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10122769A DE10122769A1 (de) | 2001-05-10 | 2001-05-10 | Gefrierschutzmittelkonzentrate enthaltend den Farbstoff C.I. Reactive Violet 5 |
| PCT/EP2002/004784 WO2002090462A1 (de) | 2001-05-10 | 2002-05-02 | Gefrierschutzmittelkonzentrate enthaltend den farbstoff c.i. reactive violet 5 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20034959D0 NO20034959D0 (no) | 2003-11-07 |
| NO20034959L NO20034959L (no) | 2003-11-07 |
| NO333717B1 true NO333717B1 (no) | 2013-09-02 |
Family
ID=7684318
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20034959A NO333717B1 (no) | 2001-05-10 | 2003-11-07 | Anti-fryskonsentrat inneholdende fargestoffet C.I. Reactive Violet 5, fremstilling og anvendelse derav, og vandig klar-til-bruk-kjolemiddelpreparat omfattende slikt konsentrat |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6818147B2 (cs) |
| EP (1) | EP1390438B1 (cs) |
| JP (1) | JP2004530017A (cs) |
| KR (1) | KR20040002940A (cs) |
| CN (1) | CN1219845C (cs) |
| AR (1) | AR033472A1 (cs) |
| AT (1) | ATE283328T1 (cs) |
| BR (1) | BR0209293B1 (cs) |
| CA (1) | CA2445792C (cs) |
| CZ (1) | CZ299952B6 (cs) |
| DE (2) | DE10122769A1 (cs) |
| ES (1) | ES2233830T3 (cs) |
| HU (1) | HU229647B1 (cs) |
| MX (1) | MXPA03009001A (cs) |
| NO (1) | NO333717B1 (cs) |
| PL (1) | PL200841B1 (cs) |
| PT (1) | PT1390438E (cs) |
| SK (1) | SK286675B6 (cs) |
| WO (1) | WO2002090462A1 (cs) |
| ZA (1) | ZA200309538B (cs) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004281106A (ja) * | 2003-03-13 | 2004-10-07 | Nissan Motor Co Ltd | 燃料電池スタック用冷却液組成物 |
| AU2003248060A1 (en) | 2003-07-11 | 2005-01-28 | Shishiai-Kabushikigaisha | Cooling fluid composition for fuel battery |
| KR100422066B1 (ko) * | 2003-07-16 | 2004-03-10 | 김영남 | 보일러용 난방수 조성물 |
| JP2007511646A (ja) * | 2003-11-13 | 2007-05-10 | ブラディサブ ミロバノビック | 凍結および腐食に対する無毒性水性溶液および利用された凍結防止剤の再生剤 |
| JP4737585B2 (ja) * | 2003-12-04 | 2011-08-03 | 本田技研工業株式会社 | 不凍液 |
| JP2005325300A (ja) * | 2004-05-17 | 2005-11-24 | Toyota Motor Corp | 冷却液組成物 |
| CN1297623C (zh) * | 2004-07-23 | 2007-01-31 | 中国石油化工股份有限公司 | 一种提高发动机冷却液稳定性的方法 |
| ATE477600T1 (de) | 2004-09-08 | 2010-08-15 | Honeywell Int Inc | Farbbehandelte ionenaustauscherharze, herstellungsverfahren, damit versehene wärmeübertragungssysteme und -anordnungen und verwendungsverfahren |
| KR101247537B1 (ko) | 2004-09-08 | 2013-03-26 | 프레스톤 프로닥츠 코포레이션 | 처리된 이온 교환 수지, 그것의 제조방법, 그것을 함유한어셈블리 및 열 전달 시스템 및 그것의 사용방법 |
| US8658326B2 (en) | 2004-09-08 | 2014-02-25 | Prestone Products Corporation | Heat transfer system, fluid, and method |
| US7985349B2 (en) | 2004-09-08 | 2011-07-26 | Honeywell International Inc. | Non-conductive colored heat transfer fluids |
| NZ553674A (en) | 2004-09-08 | 2010-12-24 | Honeywell Int Inc | Corrosion inhibitors, corrosion inhibiting heat transfer fluids, and the use thereof |
| EP1816177A4 (en) * | 2004-10-25 | 2010-10-06 | Shishiai Kk | FREEZER AND COOLANT |
| US20060186371A1 (en) * | 2005-02-22 | 2006-08-24 | Roy Perlove | Heat exchange fluid with coloring agent |
| DE502006009393D1 (de) | 2005-02-28 | 2011-06-09 | Basf Se | Glyzerinhaltige gefrierschutzmittelkonzentrate mit korrisionsschutz |
| WO2006103757A1 (ja) * | 2005-03-30 | 2006-10-05 | Shishiai-Kabushikigaisha | 燃料電池用冷却液組成物 |
| ES2378245T3 (es) | 2005-08-12 | 2012-04-10 | Prestone Products Corporation | Método para estabilizar un concentrado de refrigerante de motor y evitar la formación de sal de agua dura con la dilución |
| EP1941076B1 (en) * | 2005-10-25 | 2013-03-27 | Prestone Products Corporation | Heat transfer fluid compositions for cooling systems containing magnesium or magnesium alloys |
| CN101395241A (zh) * | 2006-03-31 | 2009-03-25 | Cci株式会社 | 冷却剂组合物 |
| US20090250654A1 (en) * | 2007-06-28 | 2009-10-08 | Chevron U.S.A. Inc. | Antifreeze concentrate and coolant compositions and preparation thereof |
| JP5535512B2 (ja) * | 2009-03-31 | 2014-07-02 | シーシーアイ株式会社 | 冷却液組成物 |
| US20100270494A1 (en) * | 2009-04-22 | 2010-10-28 | Chevron U.S.A. Inc. | Hot test fluid containing vapor phase inhibition |
| US20100270493A1 (en) * | 2009-04-22 | 2010-10-28 | Chevron U.S.A. Inc. | Hot test fluid containing vapor phase inhibition protection for ferrous as well as aluminum alloys |
| CN101899287B (zh) * | 2010-07-16 | 2015-08-26 | 中国石油化工股份有限公司 | 太阳能集热管导热液 |
| DE102012022246B4 (de) * | 2012-11-14 | 2014-07-10 | Sew-Eurodrive Gmbh & Co Kg | Vorrichtung, aufweisend ein Gehäuseteil und ein weiteres Teil |
| KR102241565B1 (ko) * | 2013-02-13 | 2021-04-16 | 바스프 에스이 | 내식성 부동 농축물 및 이로부터 제조된 수성 냉각제 조성물 |
| US9540558B2 (en) | 2013-06-12 | 2017-01-10 | Ashland Licensing And Intellectual Property, Llc | Extended operation engine coolant composition |
| JP6339442B2 (ja) * | 2014-08-01 | 2018-06-06 | シーシーアイ株式会社 | 着色冷却液組成物 |
| CN104250545B (zh) * | 2014-10-16 | 2017-06-06 | 诺泰生物科技(合肥)有限公司 | 一种甘油基防冻液 |
| DE102014116634B4 (de) * | 2014-11-13 | 2018-04-26 | Stockmeier Chemie GmbH & Co.KG | Verwendung eines Gemisches als Frostschutzkonzentrat oder Frostschutzmittel |
| CN104327805A (zh) * | 2014-11-19 | 2015-02-04 | 柳州市潮林机械有限公司 | 机车防冻液 |
| CN106398655A (zh) * | 2016-08-30 | 2017-02-15 | 天津箭牌石油化工有限公司 | 无水型防冻液及其制备方法 |
| EP3865552A1 (en) * | 2020-02-11 | 2021-08-18 | Arteco NV | Heat-transfer fluid with low conductivity comprising an amide inhibitor, methods for its preparation and uses thereof |
| US20240207028A1 (en) * | 2021-04-26 | 2024-06-27 | King's College London | Tip for a vibrating scaler and a vibrating scaler |
| EP4464757A1 (en) | 2023-05-17 | 2024-11-20 | Basf Se | Novel coolant with low electrical conductivity |
| EP4484519A1 (de) | 2023-06-28 | 2025-01-01 | Basf Se | Neue anwendungen für kühlmittel |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5725794A (en) * | 1997-03-13 | 1998-03-10 | Milliken Research Corporation | Antifreeze composition containing poly (oxyalkylene) -substituted colorant |
| US5789515A (en) * | 1997-03-13 | 1998-08-04 | Milliken Research Corporation | Polysiloxane-poly(oxyalkylene) copolymer-substituted colorant |
| US5723060A (en) | 1997-03-13 | 1998-03-03 | Milliken Research Corporation | Antifreeze composition |
| EP1087004A1 (en) * | 1999-07-16 | 2001-03-28 | Texaco Development Corporation | Synergistic combinations of carboxylates for use as freezing point depressants and corrosion inhibitors in heat transfer fluids |
-
2001
- 2001-05-10 DE DE10122769A patent/DE10122769A1/de not_active Withdrawn
-
2002
- 2002-04-25 AR ARP020101497A patent/AR033472A1/es not_active Application Discontinuation
- 2002-05-02 DE DE50201627T patent/DE50201627D1/de not_active Expired - Lifetime
- 2002-05-02 ES ES02740549T patent/ES2233830T3/es not_active Expired - Lifetime
- 2002-05-02 CN CNB028095197A patent/CN1219845C/zh not_active Expired - Fee Related
- 2002-05-02 SK SK1370-2003A patent/SK286675B6/sk not_active IP Right Cessation
- 2002-05-02 US US10/473,807 patent/US6818147B2/en not_active Expired - Lifetime
- 2002-05-02 PL PL366454A patent/PL200841B1/pl unknown
- 2002-05-02 PT PT02740549T patent/PT1390438E/pt unknown
- 2002-05-02 AT AT02740549T patent/ATE283328T1/de active
- 2002-05-02 JP JP2002587530A patent/JP2004530017A/ja not_active Withdrawn
- 2002-05-02 KR KR10-2003-7014480A patent/KR20040002940A/ko not_active Withdrawn
- 2002-05-02 MX MXPA03009001A patent/MXPA03009001A/es active IP Right Grant
- 2002-05-02 WO PCT/EP2002/004784 patent/WO2002090462A1/de active IP Right Grant
- 2002-05-02 CZ CZ20032949A patent/CZ299952B6/cs not_active IP Right Cessation
- 2002-05-02 HU HU0400093A patent/HU229647B1/hu not_active IP Right Cessation
- 2002-05-02 CA CA2445792A patent/CA2445792C/en not_active Expired - Fee Related
- 2002-05-02 BR BRPI0209293-0A patent/BR0209293B1/pt not_active IP Right Cessation
- 2002-05-02 EP EP02740549A patent/EP1390438B1/de not_active Expired - Lifetime
-
2003
- 2003-11-07 NO NO20034959A patent/NO333717B1/no not_active IP Right Cessation
- 2003-12-09 ZA ZA2003/09538A patent/ZA200309538B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NO20034959D0 (no) | 2003-11-07 |
| US20040119044A1 (en) | 2004-06-24 |
| DE10122769A1 (de) | 2002-11-14 |
| ZA200309538B (en) | 2005-02-23 |
| ATE283328T1 (de) | 2004-12-15 |
| NO20034959L (no) | 2003-11-07 |
| SK286675B6 (sk) | 2009-03-05 |
| US6818147B2 (en) | 2004-11-16 |
| HUP0400093A3 (en) | 2012-05-29 |
| BR0209293B1 (pt) | 2012-06-26 |
| AR033472A1 (es) | 2003-12-17 |
| MXPA03009001A (es) | 2004-02-12 |
| CN1507486A (zh) | 2004-06-23 |
| EP1390438A1 (de) | 2004-02-25 |
| PL200841B1 (pl) | 2009-02-27 |
| PT1390438E (pt) | 2005-04-29 |
| CZ299952B6 (cs) | 2009-01-07 |
| HUP0400093A2 (hu) | 2004-04-28 |
| EP1390438B1 (de) | 2004-11-24 |
| BR0209293A (pt) | 2004-07-13 |
| CA2445792C (en) | 2010-04-27 |
| JP2004530017A (ja) | 2004-09-30 |
| ES2233830T3 (es) | 2005-06-16 |
| HU229647B1 (en) | 2014-03-28 |
| DE50201627D1 (de) | 2004-12-30 |
| CA2445792A1 (en) | 2002-11-14 |
| SK13702003A3 (sk) | 2004-04-06 |
| PL366454A1 (en) | 2005-02-07 |
| KR20040002940A (ko) | 2004-01-07 |
| CN1219845C (zh) | 2005-09-21 |
| CZ20032949A3 (cs) | 2004-02-18 |
| WO2002090462A1 (de) | 2002-11-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |