GB650118A - Corrosion preventative compositions - Google Patents
Corrosion preventative compositionsInfo
- Publication number
- GB650118A GB650118A GB10391/48A GB1039148A GB650118A GB 650118 A GB650118 A GB 650118A GB 10391/48 A GB10391/48 A GB 10391/48A GB 1039148 A GB1039148 A GB 1039148A GB 650118 A GB650118 A GB 650118A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- oleate
- specified
- nitrile
- alkyl
- 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 abstract 4
- 230000007797 corrosion Effects 0.000 title 1
- 238000005260 corrosion Methods 0.000 title 1
- -1 amino hydroxy Chemical class 0.000 abstract 19
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 150000002148 esters Chemical class 0.000 abstract 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 abstract 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 150000007513 acids Chemical class 0.000 abstract 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 abstract 3
- 150000002825 nitriles Chemical class 0.000 abstract 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 abstract 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 abstract 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 abstract 2
- GWESVXSMPKAFAS-UHFFFAOYSA-N Isopropylcyclohexane Chemical compound CC(C)C1CCCCC1 GWESVXSMPKAFAS-UHFFFAOYSA-N 0.000 abstract 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 abstract 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001299 aldehydes Chemical class 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 abstract 2
- 235000015165 citric acid Nutrition 0.000 abstract 2
- 239000011248 coating agent Substances 0.000 abstract 2
- 238000000576 coating method Methods 0.000 abstract 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 abstract 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 abstract 2
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 2
- 238000001035 drying Methods 0.000 abstract 2
- 229930195729 fatty acid Natural products 0.000 abstract 2
- 239000000194 fatty acid Substances 0.000 abstract 2
- 150000004665 fatty acids Chemical class 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 abstract 2
- 239000003350 kerosene Substances 0.000 abstract 2
- 230000001050 lubricating effect Effects 0.000 abstract 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 abstract 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 abstract 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 229940049964 oleate Drugs 0.000 abstract 2
- 150000002917 oxazolidines Chemical class 0.000 abstract 2
- 150000002918 oxazolines Chemical class 0.000 abstract 2
- 239000003208 petroleum Substances 0.000 abstract 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 abstract 2
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 abstract 2
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- VBFBQEURBQANIX-UHFFFAOYSA-N (4-ethyl-2-undecyl-5h-1,3-oxazol-4-yl)methanol Chemical compound CCCCCCCCCCCC1=NC(CC)(CO)CO1 VBFBQEURBQANIX-UHFFFAOYSA-N 0.000 abstract 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 abstract 1
- FXCMLMVIAOZXRA-UHFFFAOYSA-N 1,2,3-tri(propan-2-yl)naphthalene Chemical compound C1=CC=C2C(C(C)C)=C(C(C)C)C(C(C)C)=CC2=C1 FXCMLMVIAOZXRA-UHFFFAOYSA-N 0.000 abstract 1
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 abstract 1
- KHYHYMMNYYTHRW-UHFFFAOYSA-N 2,4-diheptyl-1,3-oxazole Chemical compound C(CCCCCC)C=1N=C(OC1)CCCCCCC KHYHYMMNYYTHRW-UHFFFAOYSA-N 0.000 abstract 1
- LLONSWVFGFTIFG-UHFFFAOYSA-N 2-(2-ethoxyethoxy)octanenitrile Chemical compound C(C)OCCOC(C#N)CCCCCC LLONSWVFGFTIFG-UHFFFAOYSA-N 0.000 abstract 1
- IJIZXKDONYUMSH-UHFFFAOYSA-N 2-(ethoxymethoxy)acetonitrile Chemical compound C(C)OCOCC#N IJIZXKDONYUMSH-UHFFFAOYSA-N 0.000 abstract 1
- MCDDMVNPBJHHHJ-UHFFFAOYSA-N 2-(methoxymethoxy)acetonitrile Chemical compound COCOCC#N MCDDMVNPBJHHHJ-UHFFFAOYSA-N 0.000 abstract 1
- QHKGDMNPQAZMKD-UHFFFAOYSA-N 2-amino-2-methylbutan-1-ol Chemical compound CCC(C)(N)CO QHKGDMNPQAZMKD-UHFFFAOYSA-N 0.000 abstract 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 abstract 1
- MMMLPDNJYOPBDC-UHFFFAOYSA-N 2-aminoheptan-3-ol Chemical compound CCCCC(O)C(C)N MMMLPDNJYOPBDC-UHFFFAOYSA-N 0.000 abstract 1
- ULAXUFGARZZKTK-UHFFFAOYSA-N 2-aminopentan-1-ol Chemical compound CCCC(N)CO ULAXUFGARZZKTK-UHFFFAOYSA-N 0.000 abstract 1
- LGYNIFWIKSEESD-UHFFFAOYSA-N 2-ethylhexanal Chemical compound CCCCC(CC)C=O LGYNIFWIKSEESD-UHFFFAOYSA-N 0.000 abstract 1
- NVSOSXIRJQBCAP-UHFFFAOYSA-N 2-heptadecyl-4,4-dimethyl-5h-1,3-oxazole Chemical compound CCCCCCCCCCCCCCCCCC1=NC(C)(C)CO1 NVSOSXIRJQBCAP-UHFFFAOYSA-N 0.000 abstract 1
- GXDHCNNESPLIKD-UHFFFAOYSA-N 2-methylhexane Natural products CCCCC(C)C GXDHCNNESPLIKD-UHFFFAOYSA-N 0.000 abstract 1
- ZUVDXBHOPUQDGV-UHFFFAOYSA-N 2-octyl-2-propyl-1,3-oxazolidine Chemical compound C(CC)C1(OCCN1)CCCCCCCC ZUVDXBHOPUQDGV-UHFFFAOYSA-N 0.000 abstract 1
- OCSXKMIYKAIBCF-UHFFFAOYSA-N 2-undecyl-4,5-dihydro-1,3-oxazole Chemical compound CCCCCCCCCCCC1=NCCO1 OCSXKMIYKAIBCF-UHFFFAOYSA-N 0.000 abstract 1
- AEXMKKGTQYQZCS-UHFFFAOYSA-N 3,3-dimethylpentane Chemical compound CCC(C)(C)CC AEXMKKGTQYQZCS-UHFFFAOYSA-N 0.000 abstract 1
- FERWBXLFSBWTDE-UHFFFAOYSA-N 3-aminobutan-2-ol Chemical compound CC(N)C(C)O FERWBXLFSBWTDE-UHFFFAOYSA-N 0.000 abstract 1
- BKFGLDUWYUYHRF-UHFFFAOYSA-N 3-aminopentan-2-ol Chemical compound CCC(N)C(C)O BKFGLDUWYUYHRF-UHFFFAOYSA-N 0.000 abstract 1
- AJGJIVXWNHSXTC-UHFFFAOYSA-N 3-butyl-4-propyl-1,2-oxazole Chemical compound C(CC)C=1C(=NOC1)CCCC AJGJIVXWNHSXTC-UHFFFAOYSA-N 0.000 abstract 1
- DYCMSEKHDGYYBF-UHFFFAOYSA-N 4,4-dimethyl-5-phenyl-2-undecyl-5H-1,3-oxazole Chemical compound C(CCCCCCCCCC)C=1OC(C(N1)(C)C)C1=CC=CC=C1 DYCMSEKHDGYYBF-UHFFFAOYSA-N 0.000 abstract 1
- PNCLISPTGOFJAK-UHFFFAOYSA-N 4,5-diethyl-2-octyl-1,3-oxazole Chemical compound C(C)C1=C(N=C(O1)CCCCCCCC)CC PNCLISPTGOFJAK-UHFFFAOYSA-N 0.000 abstract 1
- BGBPWYDGOVTWPG-UHFFFAOYSA-N 4-(dodecoxymethyl)-4-methyl-2-undecyl-5H-1,3-oxazole Chemical compound C(CCCCCCCCCC)C=1OCC(N1)(COCCCCCCCCCCCC)C BGBPWYDGOVTWPG-UHFFFAOYSA-N 0.000 abstract 1
- IOYVGJNAPMXLLT-UHFFFAOYSA-N 4-aminohexan-3-ol Chemical compound CCC(N)C(O)CC IOYVGJNAPMXLLT-UHFFFAOYSA-N 0.000 abstract 1
- WZVBMYHBWXOBIO-WKKCZKGXSA-N C(CCCCCCCC=C/CCCCCCCC)(=O)O.C(CCCCCCCC=C/CCCCCCCC)(=O)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O Chemical compound C(CCCCCCCC=C/CCCCCCCC)(=O)O.C(CCCCCCCC=C/CCCCCCCC)(=O)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O.C([C@H](O)[C@H](O)CO)O WZVBMYHBWXOBIO-WKKCZKGXSA-N 0.000 abstract 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004386 Erythritol Substances 0.000 abstract 1
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 229930195725 Mannitol Natural products 0.000 abstract 1
- 241000158728 Meliaceae Species 0.000 abstract 1
- 239000004264 Petrolatum Substances 0.000 abstract 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910000831 Steel Inorganic materials 0.000 abstract 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 abstract 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001983 dialkylethers Chemical class 0.000 abstract 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 abstract 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 abstract 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 abstract 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 abstract 1
- 235000019414 erythritol Nutrition 0.000 abstract 1
- 229940009714 erythritol Drugs 0.000 abstract 1
- AZXVZUBIFYQWJK-KWRJMZDGSA-N ethyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OCC AZXVZUBIFYQWJK-KWRJMZDGSA-N 0.000 abstract 1
- 239000007789 gas Substances 0.000 abstract 1
- 235000011187 glycerol Nutrition 0.000 abstract 1
- RZRNAYUHWVFMIP-HXUWFJFHSA-N glycerol monolinoleate Natural products CCCCCCCCC=CCCCCCCCC(=O)OC[C@H](O)CO RZRNAYUHWVFMIP-HXUWFJFHSA-N 0.000 abstract 1
- 239000004519 grease Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000594 mannitol Substances 0.000 abstract 1
- 235000010355 mannitol Nutrition 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 150000002739 metals Chemical class 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 abstract 1
- 239000002480 mineral oil Substances 0.000 abstract 1
- 235000010446 mineral oil Nutrition 0.000 abstract 1
- AYTIAPQIRMHXML-KVVVOXFISA-N n-cyclohexylcyclohexanamine;(z)-octadec-9-enoic acid Chemical compound C1CCCCC1NC1CCCCC1.CCCCCCCC\C=C/CCCCCCCC(O)=O AYTIAPQIRMHXML-KVVVOXFISA-N 0.000 abstract 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 abstract 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 abstract 1
- 229940038384 octadecane Drugs 0.000 abstract 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 125000001477 organic nitrogen group Chemical group 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 239000012188 paraffin wax Substances 0.000 abstract 1
- 229940059574 pentaerithrityl Drugs 0.000 abstract 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 abstract 1
- 229940066842 petrolatum Drugs 0.000 abstract 1
- 235000019271 petrolatum Nutrition 0.000 abstract 1
- 229920000098 polyolefin Polymers 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 239000001593 sorbitan monooleate Substances 0.000 abstract 1
- 235000011069 sorbitan monooleate Nutrition 0.000 abstract 1
- 229940035049 sorbitan monooleate Drugs 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 239000010959 steel Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004291 sulphur dioxide Substances 0.000 abstract 1
- 235000010269 sulphur dioxide Nutrition 0.000 abstract 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid group Chemical group C(\C(\C)=C\C)(=O)O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 abstract 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
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- C—CHEMISTRY; METALLURGY
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- General Chemical & Material Sciences (AREA)
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- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Lubricants (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Oxazolines are made by (1) heating amino hydroxy compounds with fatty acids at 150 DEG to 170 DEG C. and then heating the so-formed amide at around 250 DEG C.; (2) reacting an amino hydroxy compound with a nitrile. Oxazolidines are made by reacting one mol. of an amino monohydric alcohol with one mol. of an aldehyde. Specified aminohydroxy compounds are mono-ethanol amine, propanol amine, 2-methyl - 2 - amino - 1 - propanol, 2 - ethyl - 2 - amino - 1 - propanol, 2 - amino - 1 - butanol, 2 - amino - 1 - pentanol, 2 - amino - 1 - ethanol, 2 - amino - 3 - butanol, 3 - amino - 4 - pentanol, 3-amino-4-hexanol and 2-amino-3-heptanol. Specified fatty acids are acetic, propionic, butyric, caproic, heptoic, caprylic, pelargonic, capric, undecylic, lauric, tridecylic, myristic, pentadecylic, palmitic, stearic, nonadecylic, arachidic, acrylic, butenic, crotonic, pentenic, tiglic, hexenic, teracrylic, hypogeic, oleic and erucic. The nitriles may be alkyl, aryl, alkoxyalkane, aralkoxy, alkoxyalkane nitrile, e.g. (ethoxy methoxy) ethane nitrile, (ethoxy ethoxy) octane nitrile, (methoxy methoxy) ethane nitrile and nitriles of hexane, octane, decane, dodecane, tetradecane, hexadecane and octadecane. Specified aldehydes are formaldehyde, acetaldehyde, butyraldehyde, isobutyraldehyde, benzaldehyde, ethyl hexaldehyde, and propionaldehyde. Salts of the above oxazolines and oxazolidines are used in non-drying coating and lubricating compositions. Specification 607,013, [Group III], is referred to.ALSO:A non-drying metal coating and lubricating composition comprises a non-aqueous organic medium containing in an amount of not more than 10 per cent by weight of the total composition a polyhydric alcohol partial ester having at least 12 carbon atoms in the molecule, a melting point below 200 DEG F. and at least two free hydroxyl radicals separated by not more than three intervening atoms, and a salt of an organic nitrogen-containing base and an organic acid to solubilize the ester in the medium, the salt being present in the smallest amount necessary to hold the partial ester in solution at any chosen temperature. The esters may be derived from alcohols such as glycerine, erythritol, penta-erythritol, mannitol, sorbitol, sorbitan, or citric acid, and acids such as capric, citronellic, undecylic, undecylenic, lauric, tridecylic, myristic, myristolenic, pentadecylic, palmitic, palmitolenic, therapinic, oleic, elaidic, erucic, stearic, abietic, naphthenic, sulphonic, alkyl sulphuric, alkyl phosphoric, or phosphoric. Specified esters are glycerol mono-oleate, sorbitan mono-oleate, and penta-erythritol di-oleate. The medium may be mineral oil or spirit, seal oil, paraffin, petrolatum, soap thickened grease, petroleum naphtha cuts, gas oils, waxes, kerosene sulphur dioxide extract, benzene, o-, p-, m-xylene, cumene, butyl benzene, n-hexane, dimethyl pentane, octane, nonane, undecane, dodecane, cyclohexane, methylcyclohexane, isopropylcyclohexane, chlorinated kerosene, carbon tetrachloride, chloroform, olefin polymers, polymerized alkylene oxides, 2-ethylhexyl sebacate, ethyl ricinoleate or dioctyl phthalate. The salts may be those formed by combining any of the following acids, capric, lauric, myristic, palmitic, stearic, hydroxy stearic, ricinoleic, oleic, lactic, alkyl malonic, alkyl succinic, citric, amyl sulphonic, tri-isopropyl naphthalene sulphonic or petroleum sulphonic acid (mahogany acids) with any of the following bases, monocyclohexyl-, dicyclohexyl-, tricyclohexyl-, cyclohexylolelyl - diamyl cyclohexylamine; ethyloctyl-, dioctyl-, dibutyl-, propyl butyl-isoxazole; 2-heptyl-, tridecyl-, 2-octyl-, 2 - hendecyl - (4 - hydroxylmethyl - 4 - ethyloxazoline); 2-octyl-, 2-hendecyl-oxazoline; 2-hendecyl -, 2 - heptadecyl - (4,4 - dimethyloxazoline); 2 - pentyl - 4,5 - dimethyl - 4 - hexanooxyethyl - 2 - oxazoline; 2 - undecyl - 4-methyl - 4 - lauroxymethyl - 2 - oxazoline; 2 - undecyl - 4,4 - dimethyl - 5 - phenyl - 2-oxazoline; methyl-, ethyl-, diethyl-octyloxazole; diheptyloxazole; or butyl-, diethyl-, diheptyl-, ethyloctyl-, propyloctyl-oxazolidine. Specified salts are dicyclohexyl ammonium oleate, dicyclohexylamine oleate, diisopropylammonium oleate. Metals specified are steel and aluminium. Specification 607,013 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US744536A US2564422A (en) | 1947-04-28 | 1947-04-28 | Corrosion preventive composition |
Publications (1)
Publication Number | Publication Date |
---|---|
GB650118A true GB650118A (en) | 1951-02-14 |
Family
ID=24993068
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB10391/48A Expired GB650118A (en) | 1947-04-28 | 1948-04-14 | Corrosion preventative compositions |
Country Status (2)
Country | Link |
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US (1) | US2564422A (en) |
GB (1) | GB650118A (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2597117A1 (en) * | 1986-04-09 | 1987-10-16 | Shell Int Research | ANTI-CORROSION COMPOSITION |
EP0277711A1 (en) * | 1987-01-27 | 1988-08-10 | Imperial Chemical Industries Plc | Corrosion inhibition |
WO1995004800A1 (en) * | 1993-08-07 | 1995-02-16 | Ina Wälzlager Schaeffler Kg | Preservative oil for ferrous material components |
US5833722A (en) * | 1994-12-13 | 1998-11-10 | Exxon Chemical Patents, Inc. | Fuel oil compositions with improved lubricity properties |
CN104277654A (en) * | 2014-09-28 | 2015-01-14 | 太阳化学(海安)有限公司 | Novel metal paint and preparation method thereof |
US20180340080A1 (en) * | 2014-07-02 | 2018-11-29 | Vci Coatings, Llc | Corrosion resistant coatings for metal surfaces |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2759894A (en) * | 1951-07-27 | 1956-08-21 | Exxon Research Engineering Co | Rust inhibitor |
US2711374A (en) * | 1951-08-31 | 1955-06-21 | Exxon Research Engineering Co | Corrosion inhibiting composition |
US2716611A (en) * | 1951-10-30 | 1955-08-30 | Exxon Research Engineering Co | Rust preventive composition |
DE974140C (en) * | 1952-05-03 | 1960-09-29 | Rhein Chemie G M B H | Process for improving the solubility and miscibility of naphthenic acid salts which contain monovalent or polyvalent cations in or with hydrocarbons |
DE974483C (en) * | 1952-05-03 | 1961-01-12 | Rhein Chemie G M B H | Process for improving the solubility and miscibility of naphthenic acid salts which contain monovalent or polyvalent cations in or with hydrocarbons |
US2736658A (en) * | 1952-07-23 | 1956-02-28 | Armour & Co | Method of protecting metal surfaces from corrosion and corrosion inhibitor compositions |
US2830021A (en) * | 1953-12-28 | 1958-04-08 | Gulf Oil Corp | Lubricant containing an aliphatic amine salt of monoalkyl ester of a dimeric acid |
US2980613A (en) * | 1956-10-11 | 1961-04-18 | Sun Oil Co | Sulfur-containing lubricant inhibited against staining |
US4113635A (en) * | 1971-12-13 | 1978-09-12 | Nippon Steel Corporation | Rust-proof lubricant compositions |
DE3540246A1 (en) * | 1985-11-13 | 1987-05-14 | Henkel Kgaa | USE OF ALKOXYHYDROXY FATTY ACIDS AS CORROSION INHIBITORS IN OILS AND OIL-BASED EMULSIONS |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2167867A (en) * | 1936-05-07 | 1939-08-01 | Du Pont | Lubricant |
US2308282A (en) * | 1937-12-28 | 1943-01-12 | Us Rubber Co | Corrosion inhibitor |
US2215038A (en) * | 1939-04-29 | 1940-09-17 | Reichhold Chemicals Inc | Aminohydroxy compounds and derivatives and process of making the same |
US2382699A (en) * | 1941-01-02 | 1945-08-14 | Standard Oil Dev Co | Slushing oil compositions |
US2312414A (en) * | 1941-09-04 | 1943-03-02 | American Cyanamid Co | Process for concentrating ore materials |
US2398193A (en) * | 1943-11-30 | 1946-04-09 | Standard Oil Co | Lubricant |
US2402791A (en) * | 1944-05-11 | 1946-06-25 | Commercial Solvents Corp | Reaction product of oxazolines |
US2434490A (en) * | 1944-12-30 | 1948-01-13 | Standard Oil Dev Co | Rust preventive lubricating oil compositions |
US2442581A (en) * | 1945-07-28 | 1948-06-01 | Tide Water Associated Oil Comp | Rust-preventive composition |
US2412634A (en) * | 1945-12-11 | 1946-12-17 | Standard Oil Co | Lubricant |
US2442582A (en) * | 1946-08-10 | 1948-06-01 | Tide Water Associated Oil Comp | Oxazoline reaction products |
-
1947
- 1947-04-28 US US744536A patent/US2564422A/en not_active Expired - Lifetime
-
1948
- 1948-04-14 GB GB10391/48A patent/GB650118A/en not_active Expired
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2597117A1 (en) * | 1986-04-09 | 1987-10-16 | Shell Int Research | ANTI-CORROSION COMPOSITION |
EP0277711A1 (en) * | 1987-01-27 | 1988-08-10 | Imperial Chemical Industries Plc | Corrosion inhibition |
US4814010A (en) * | 1987-01-27 | 1989-03-21 | Imperial Chemical Industries Plc | Corrosion inhibition |
WO1995004800A1 (en) * | 1993-08-07 | 1995-02-16 | Ina Wälzlager Schaeffler Kg | Preservative oil for ferrous material components |
US5833722A (en) * | 1994-12-13 | 1998-11-10 | Exxon Chemical Patents, Inc. | Fuel oil compositions with improved lubricity properties |
US5858028A (en) * | 1994-12-13 | 1999-01-12 | Exxon Chemical Patents Inc. | Fuel oil compositions |
US6010545A (en) * | 1994-12-13 | 2000-01-04 | Exxon Chemical Patents, Inc. | Fuel oil compositions |
US20180340080A1 (en) * | 2014-07-02 | 2018-11-29 | Vci Coatings, Llc | Corrosion resistant coatings for metal surfaces |
US10669434B2 (en) * | 2014-07-02 | 2020-06-02 | Vci Coatings, Llc | Corrosion resistant coatings for metal surfaces |
CN104277654A (en) * | 2014-09-28 | 2015-01-14 | 太阳化学(海安)有限公司 | Novel metal paint and preparation method thereof |
Also Published As
Publication number | Publication date |
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US2564422A (en) | 1951-08-14 |
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