US2920030A - Method of preventing corrosion - Google Patents
Method of preventing corrosion Download PDFInfo
- Publication number
- US2920030A US2920030A US534627A US53462755A US2920030A US 2920030 A US2920030 A US 2920030A US 534627 A US534627 A US 534627A US 53462755 A US53462755 A US 53462755A US 2920030 A US2920030 A US 2920030A
- Authority
- US
- United States
- Prior art keywords
- oil
- corrosion
- distillation
- distillate product
- corrosion inhibitor
- 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 - Lifetime
Links
- 238000005260 corrosion Methods 0.000 title claims description 94
- 230000007797 corrosion Effects 0.000 title claims description 94
- 238000000034 method Methods 0.000 title claims description 22
- 239000003112 inhibitor Substances 0.000 claims description 58
- 238000004821 distillation Methods 0.000 claims description 39
- 150000003839 salts Chemical class 0.000 claims description 27
- 230000000717 retained effect Effects 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 claims description 9
- 229920000768 polyamine Polymers 0.000 claims description 7
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- 150000003973 alkyl amines Chemical class 0.000 claims description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 239000011369 resultant mixture Substances 0.000 claims description 6
- 238000007670 refining Methods 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 239000000047 product Substances 0.000 description 47
- 239000002253 acid Substances 0.000 description 23
- 239000003921 oil Substances 0.000 description 22
- 235000019198 oils Nutrition 0.000 description 22
- 239000003502 gasoline Substances 0.000 description 15
- 238000001816 cooling Methods 0.000 description 11
- 150000007524 organic acids Chemical class 0.000 description 10
- 230000002378 acidificating effect Effects 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000979 retarding effect Effects 0.000 description 6
- SPBJUTVLDJRGSY-UHFFFAOYSA-N 1-heptadecyl-4,5-dihydroimidazole Chemical compound CCCCCCCCCCCCCCCCCN1CCN=C1 SPBJUTVLDJRGSY-UHFFFAOYSA-N 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 5
- 125000002947 alkylene group Chemical group 0.000 description 5
- 239000003518 caustics Substances 0.000 description 5
- 150000002462 imidazolines Chemical class 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 239000000295 fuel oil Substances 0.000 description 4
- 239000010687 lubricating oil Substances 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000005336 cracking Methods 0.000 description 3
- 239000010779 crude oil Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 239000002283 diesel fuel Substances 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- -1 etc. Chemical compound 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
- JPZYXGPCHFZBHO-UHFFFAOYSA-N 1-aminopentadecane Chemical compound CCCCCCCCCCCCCCCN JPZYXGPCHFZBHO-UHFFFAOYSA-N 0.000 description 1
- SHDHSEXMMNYEQW-UHFFFAOYSA-N 2-dodecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCCC1=NCCN1 SHDHSEXMMNYEQW-UHFFFAOYSA-N 0.000 description 1
- BJSBMAVDTBVDRO-UHFFFAOYSA-N 2-nonyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCC1=NCCN1 BJSBMAVDTBVDRO-UHFFFAOYSA-N 0.000 description 1
- VRIBUWOAMIKHGX-UHFFFAOYSA-N 2-octadecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCCCCCCCCC1=NCCN1 VRIBUWOAMIKHGX-UHFFFAOYSA-N 0.000 description 1
- RPEKHMWFNMGIHP-UHFFFAOYSA-N 2-octyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCC1=NCCN1 RPEKHMWFNMGIHP-UHFFFAOYSA-N 0.000 description 1
- UKJKJYIQYXYUSG-UHFFFAOYSA-N 2-tridecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCCCC1=NCCN1 UKJKJYIQYXYUSG-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 150000001896 cresols Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- KAJZYANLDWUIES-UHFFFAOYSA-N heptadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCN KAJZYANLDWUIES-UHFFFAOYSA-N 0.000 description 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- BUHXFUSLEBPCEB-UHFFFAOYSA-N icosan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCN BUHXFUSLEBPCEB-UHFFFAOYSA-N 0.000 description 1
- 125000002636 imidazolinyl group Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- INAMEDPXUAWNKL-UHFFFAOYSA-N nonadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCN INAMEDPXUAWNKL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- LBOHISOWGKIIKX-UHFFFAOYSA-M potassium;2-methylpropanoate Chemical compound [K+].CC(C)C([O-])=O LBOHISOWGKIIKX-UHFFFAOYSA-M 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000010736 steam turbine oil Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002311 subsequent effect Effects 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- ABVVEAHYODGCLZ-UHFFFAOYSA-N tridecan-1-amine Chemical compound CCCCCCCCCCCCCN ABVVEAHYODGCLZ-UHFFFAOYSA-N 0.000 description 1
- QFKMMXYLAPZKIB-UHFFFAOYSA-N undecan-1-amine Chemical compound CCCCCCCCCCCN QFKMMXYLAPZKIB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G7/00—Distillation of hydrocarbon oils
- C10G7/10—Inhibiting corrosion during distillation
Definitions
- This invention relates to a novel method of preventing United States PatentiO corrosion of, plant equipment used in the refining of an organic liquid. More particularly it is directed to a process 1n which an organic liquid is subjected to distillation and a distilate product is collected and then 'subjected to treatment with an alkaline agent, after which 1t1s sent to storage.
- a serious problem encountered during the refining of .oils is corrosion of the plant equipment.
- crude, reduced crude, gas oil, etc. are subjected to cracking, either in the presence or absence of a catalyst, in
- the gasoline generally is recovered as an overhead fraction from the distillation zone, while the fuel .oil, lube oil and other fractions may be recovered as side cuts from the distillation zone. These fractions then are cooled, condensed and sent to collecting equipment.
- the cracked products contain sulfur or sulfur compounds and other acidic components which subsequently are removed in an alkaline treating step, after which the product is sent to storage;
- the corrosion inhibitor employed in this step of the process is an oil soluble basic corrosion inhibitor and therefore is not removed during subsequent treatment of the distillate product with an alkaline agent.
- an organic acid is commingled with the distillate product in a concentration sufiicient to .form a salt of the basic corrosion inhibitor, and the resulting salt serves as an inhibitor to retard corrosion of the storage equipment into which the treated oil is passed.
- the basic corrosion inhibitor is effective in retarding corrosion of the distillation, connecting cooling and collecting equipment butvit is not effective in retarding corrosion of the storage equipment.
- the reason why the basic corrosion inhibitor is not effective in retarding corrosion of the storage tanks is not completely understood.
- One possible explanation is that the distillation, cooling and collecting is effected in the absence of air, whereas the storage of the oil is effected in the presence of air. Air is introduced into the storage tanks during gaging of the tanks or in other ways.
- some alkaline treating processes employ air or oxygen during the treating step, and the air or oxygen may be retained in the treated product. Applicant does not intend to be limited to this specific explanation. Regardless of the reason, this phenomenon has been demonstrated in actual refinery runs.
- a basic corrosion inhibitor is employed in the first stepof the process and is not removed during method of preventing corrosion of distillation and con- 55 necting collecting equipment and of subsequent storage equipment used in'the refining of an organic liquid, wherein said organic liquid is subjected to treatment with an alkaline agent between the collecting and storage thereof, which comprises effecting said distillation in the presence of a basic corrosion inhibitor which is in part retained in a.
- distillate product of said distillation whereby the corrosion of said distillation and of said collecting equipment is retarded, thereafter subjecting said distillate product to treatment with an alkaline agent and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling an organic acid with the treated distillate product containing the basic corrosion inhibitor in a concentration sufiicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
- the present invention is used in preventing corrosion of .distillation and condensing, cooling and collecting equipment, as well as of sub-sequent storage equipment used in the handling of oil containing corrosive components regardless of the source of said oil.
- the basic corrosion inhibitor may be added directly to the distillation zone or it maybe commingled with the oil being supplied thereto.
- a preferred method is to inject the basic corrosion inhibitor into the upper portion of the distillation zone. It is believed that the corrosion inhibitor forms a film on the inner surface. of the metal and thereby prevents attack by Water, water vapor, hydrogen sulfide or other acidic components.
- the basic corrosion inhibitor is retained in part in the product and this, in turn, serves to retard corrosion of the piping, cooler, condenser, heat exchanger and receiving tanks through and-into which the distillate product is passed.
- Any suitable basic corrosion inhibitor may be employed in accordance with the present invention.
- One class of basic corrosion inhibitor comprises substituted imidazolines including particularly Z-heptadecyl imidazoline.
- Other substituted imidazolines include Z-hexyl imidazoline, Z-heptyl imidazoline, 2-octyl imidazoline, 2-nonyl imidazoline, Z-decyl imidazoline, Z-undecyl imidazoline, 2-dodecyl imidazoline, 2-tridecyl imidazoline, Z-tetradecyl imidazoline, Z-pentadecyl imidazoline, Z-hexadecyl imidazoline, 2-octadecyl imidazoline, Z-nonadecyl imidazoline, etc.
- the imidazoline may contain other substituents attached thereto, the other substituents being selected from alkyl, cycloalkyl or aryl groups as well as such groups containing oxygen, nitrogen or sulfur.
- Another class of basic corrosion inhibitor comprises oil soluble alkyl amines including decyl amine, undecyl amine, dodecyl amine, tridecyl amine, tetradecyl amine, pentadecyl amine, hexadecyl amine, heptadecyl amine, octadecyl amine, nonadecyl amine, eicosyl amine, etc.
- Still another class comprises oil soluble alkylene polyamines and particularly N-alkyl alkylene polyamines including N- alkyl propylene diamines in which the alkyl group contains at least 6 and preferably at least 10 carbon atoms.
- N-alkyl propylene diamines in which the alkyl group is derived from tallow, lauric acid, coconut oil, soya oil, etc. are available commercially at relatively inexpensive prices because they are produced as by-product.
- Duomeen T is an N-alkyl propylene diamine in which the alkyl group contains from about 12 to about 20 carbon atoms per group and mostly containing 16 to 18 carbon atoms per group. It is understood that a mixture of basic corrosion inhibitors may be employed.
- the basic corrosion inhibitor retards corrosion of the distillation and connecting cooling, condensing and collecting equipment.
- the distillate product may comprise t-he overhead fraction withdrawn from the upper portion of the distillation zone as would be the case, for example, when distilling to separate an overhead gasoline fraction from higher boiling material.
- a fuel oil or lubricating oil fraction may be separated as one or more side cuts.
- the distillate product, whether an overhead or side out fraction, is subjected to treatment with an alkaline reagent in order to remove acidic components.
- mercaptans and other acidic components are removed from gasoline by treatment 'with caustic (sodium hydroxide), potassium 'hydroxide, etc., or preferably these in admixture with a solutizing agent including, for example, alcohols, and particularly methanol or ethanol, cresols, tannin, etc., potassium isobutyrate, and others. It is understood that any suitable alkaline treating process may be employed.
- the treated distillate product is separated from the alkaline agent and the distillate product then sent to storage.
- an organic acid is comrningled with the treated distillate product on its way to storage or is introduced directly into the storage tank.
- Any suitable organic acid may be employed and preferably comprises an inexpensive organic acid.
- a number of relatively inexpensive organic acids are available commercially, these being produced as by-products.
- One such acid is marketed commercially under the trade name of VR-l Acid. This acid is a liquid at 77 F., has an acid number of about 150, an iodine number of about 36 and is a mixture of polybasic acids, having a titration equivalent weight of about 350.
- Dimer acid Another inexpensive acid is available commercially under the name of Dimer acid. It is understood that any suitable organic acid may be employed and may be either monobasic or polybasic. It generally is preferred that the acid comprises a long chain carboxylic acid and may be selected from oleic acid, linoleic acid, pa'lmitic acid, stearic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, phthalic acid, etc. As hereinbefore set forth, any suitable organic acid may be used and, when desired, a mixture of organic acids may be employed.
- the basic corrosion inhibitor is introduced in the distillation zone in a sufiicient concentration to retard corrosion thereof.
- concentration of basic corrosion inhibitor will be within the range of from about '1 to about 15 pounds per 1000 barrels of distillate product, although smaller or larger concentrations may be used.
- the corrosion inhibitor will be retained to a considerable extent in the distillate product and thereby will serve to retard corrosion of the connecting cooling, condensing and collecting equipment.
- the organic acid will be used in a concentration sufiicient to form a salt and preferably an acid salt of the basic inhibitor. This will, in turn, depend upon the basic nitrogen content of the basic corrosion inhibitor.
- the substituted imidazoline there is one basic nitrogen per molecule.
- Duomeen-T there are two basic nitrogens.
- a monocarboxylic acid it will be used in equal mol proportions with the substituted imidazoline to form the neutral salt and will be used in a larger concentration and preferably two mols to form the acid salt.
- a dicarboxylic acid with the substituted imidazoline one mol of acid per two mols of imidazoline will be used to form the neutral salt or equal mols of acid and imidazoline will be used to form the acid salt.
- the salt When using Duomeen-T, two mols of a monocarboxylic acid salt or one mol of a dicarboxylic acid will be used to form the neutral salt and a larger concentration will be used to form the acid salt. As hereinbefore set forth, the salt will effectively retard corrosion of the storage tank, as well as being retained in part in the distillate product and thereby will provide protection against subsequent metallic equipment through or into which the distillate product is passed.
- Example I It has been established that the ASTM steam turbine oil corrosion test (ASTM Designation D665-52T) correlates with the results obtained in the storage of oil in storage tanks.
- ASTM steam turbine oil corrosion test (ASTM Designation D665-52T) correlates with the results obtained in the storage of oil in storage tanks.
- a highly polished mild carbon steel rod is placed in 300 cc. of Nujol, to which 30 cc. of synthetic sea water was added, and then heated to and maintained at F. with stirring for 48 hours in a beaker open to the atmosphere;
- the basic corrosion inhibitor used in this example ws heptadecylimidazoline and was utilized in a concentration of 0.01% by weight of the Nujol. After heating for 48 hours, corrosion of the steel rod was very heavy; that; is, the rod was completely covered with corrosion.
- the neutral salt of heptadecyl imidtlZQl nc and VR-l acid using one mol of acid per two mols of imidazollne, when utilized in a concentration of 0.01% by weight of Nujol and tested in the same manner, resulted in only light corrosion (that is, onetenth or less of the steel rod was covered with rust).
- Example 11 In another series of runs similar to those described in Example I, the basic corrosion inhibitor is Duomeen- T. While this compound is eifective in retarding corrosion during distillation of the efiiuent products of thermal cracking, it is not effective in retarding corrosion in the final storage tanks.
- the Duomeen-T is introduced into the upper portion of the fractionator in a concentration of 7 pounds per 1000 barrels of the overhead fraction withdrawn from the upper portion of the fractionator.
- the overhead fraction is sent through heat exchangers into a receiver.
- the Duomeen-T serves to retard corrosion of this equipment.
- the cracked gasoline then is subjected to treatment with caustic methanol, and the treated gasoline is sent to storage.
- VR-l acid is commingled with the treated gasoline on its Way to storage in a concentration suflicient to form the acid salt of the Duomeen-T.
- a method of preventing corrosion of distillation and connecting collecting equipment and of subsequent storage equipment used in the refining of hydrocarbon oil wherein said oil is subjected to treatment with an alkaline agent between the collecting and storage thereof, which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said collecting equipment is retarded, thereafter subjecting said distillate product to treatment with an alkaline agent selected from the group consisting of sodium hydroxide and potassium hydroxide and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
- a method of preventing corrosion of distillation and connecting cooling and collecting equipment of a hydrocarbon oil cracking unit and of subsequent storage equipment which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic cor-
- both the neurosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt sewing as an inhibitor to retard corrosion of said storage equipment.
- distillate product is removed as an overhead fraction and comprises gasoline components.
- distillate product is removed as a side out and comprises components heavier than gasoline.
- a method of preventing corrosion of distillation and connecting cooling and collecting equipment of a gasoline reforming unit and of subsequent storage equip ment which comprises distilling the gasoline in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, there after commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration sufiicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
- a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil
- a method of preventing corrosion of distillation and connecting cooling and collecting equipment of a crude oil distillation unit and of subsequent storage equipment which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
- a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble al
- the method of claim 1 further characterized in that the said basic corrosion inhibitor is an N-alkyl propylene diamine in which the alkyl group contains at least 6 carbon atoms.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
was.
performed on' oil from various sources. heavy petroleum distillates, including crude oil, topped Application September 15, 1955 Serial No. 534,627
'11 Claims. (Cl. 20s47)",
No Drawing.
This invention relates to a novel method of preventing United States PatentiO corrosion of, plant equipment used in the refining of an organic liquid. More particularly it is directed to a process 1n which an organic liquid is subjected to distillation and a distilate product is collected and then 'subjected to treatment with an alkaline agent, after which 1t1s sent to storage.
A serious problem encountered during the refining of .oils is corrosion of the plant equipment.
During distillation of 0118 containlng acidic components, corrosion .occurs inthe internal surfaces of'the' distillation column and in the internal fractionating equipment including, for example, baflle plates, bubble decks, side-to-side pans, etc. Acidic components are removed from the distillation zone along with the distillateproduct and cause corrosion of the heat exchangers, coolers, condensers, etc. and of the receiving tanks, as well as of the connecting piping, through or into which the distillate product passes. The distillate product is treated with an alkaline reagent in order to remove the acidic components and then it is passed to storage. Corrosion of the storage tanks also is encountered due to the presence of water and air therein. The corrosion is further increased because all of the acidic components are'not completely removed during the alkaline treatment.
Distillation, alkaline treatment and storage of oil are For example,
crude, reduced crude, gas oil, etc., are subjected to cracking, either in the presence or absence of a catalyst, in
.order to form lower boiling materials and particularly gasoline. The product from the cracking is subjected to distillation to separate a gasoline fraction, as well as otherfractions including a fuel oil or dieselfuel fraction,
lubricating oil fraction, etc. The gasoline generally is recovered as an overhead fraction from the distillation zone, while the fuel .oil, lube oil and other fractions may be recovered as side cuts from the distillation zone. These fractions then are cooled, condensed and sent to collecting equipment. The cracked products contain sulfur or sulfur compounds and other acidic components which subsequently are removed in an alkaline treating step, after which the product is sent to storage; An-
. other illustration of a system employing distillation, alkaline treating and storage equipment includes the reform- Still another illustration includes the distillation of crude -oil or other heavy oil to separate'a gasoline fraction and/or a fuel oil or diesel fuel fraction, aswell as a lubricating oil or other fraction, and one or more of these fractions is subjected to alkaline treatment for 2,920,030 Patented Jan. 5, 1960 least a portion of the corrosion inhibitor is retained in the distillate product and thereby serves to prevent corrosion of the heat exchangers, coolers, condensers, receiving tanks 'and piping through or into which the distillate product is passed. The corrosion inhibitor employed in this step of the process is an oil soluble basic corrosion inhibitor and therefore is not removed during subsequent treatment of the distillate product with an alkaline agent. Following the alkaline treatment, an organic acid is commingled with the distillate product in a concentration sufiicient to .form a salt of the basic corrosion inhibitor, and the resulting salt serves as an inhibitor to retard corrosion of the storage equipment into which the treated oil is passed.
It has been found that the basic corrosion inhibitor is effective in retarding corrosion of the distillation, connecting cooling and collecting equipment butvit is not effective in retarding corrosion of the storage equipment. The reason why the basic corrosion inhibitor is not effective in retarding corrosion of the storage tanks is not completely understood. One possible explanation is that the distillation, cooling and collecting is effected in the absence of air, whereas the storage of the oil is effected in the presence of air. Air is introduced into the storage tanks during gaging of the tanks or in other ways. Furthermore, some alkaline treating processes employ air or oxygen during the treating step, and the air or oxygen may be retained in the treated product. Applicant does not intend to be limited to this specific explanation. Regardless of the reason, this phenomenon has been demonstrated in actual refinery runs.
The present invention ofiers numerous advantages. In the first place, a basic corrosion inhibitor is employed in the first stepof the process and is not removed during method of preventing corrosion of distillation and con- 55 necting collecting equipment and of subsequent storage equipment used in'the refining of an organic liquid, wherein said organic liquid is subjected to treatment with an alkaline agent between the collecting and storage thereof, which comprises effecting said distillation in the presence of a basic corrosion inhibitor which is in part retained in a. distillate product of said distillation, whereby the corrosion of said distillation and of said collecting equipment is retarded, thereafter subjecting said distillate product to treatment with an alkaline agent and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling an organic acid with the treated distillate product containing the basic corrosion inhibitor in a concentration sufiicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
As hereinbefore set forth, the present invention is used in preventing corrosion of .distillation and condensing, cooling and collecting equipment, as well as of sub-sequent storage equipment used in the handling of oil containing corrosive components regardless of the source of said oil. The basic corrosion inhibitor may be added directly to the distillation zone or it maybe commingled with the oil being supplied thereto. A preferred method is to inject the basic corrosion inhibitor into the upper portion of the distillation zone. It is believed that the corrosion inhibitor forms a film on the inner surface. of the metal and thereby prevents attack by Water, water vapor, hydrogen sulfide or other acidic components. The basic corrosion inhibitor is retained in part in the product and this, in turn, serves to retard corrosion of the piping, cooler, condenser, heat exchanger and receiving tanks through and-into which the distillate product is passed.
Any suitable basic corrosion inhibitor may be employed in accordance with the present invention. One class of basic corrosion inhibitor comprises substituted imidazolines including particularly Z-heptadecyl imidazoline. Other substituted imidazolines include Z-hexyl imidazoline, Z-heptyl imidazoline, 2-octyl imidazoline, 2-nonyl imidazoline, Z-decyl imidazoline, Z-undecyl imidazoline, 2-dodecyl imidazoline, 2-tridecyl imidazoline, Z-tetradecyl imidazoline, Z-pentadecyl imidazoline, Z-hexadecyl imidazoline, 2-octadecyl imidazoline, Z-nonadecyl imidazoline, etc. The imidazoline may contain other substituents attached thereto, the other substituents being selected from alkyl, cycloalkyl or aryl groups as well as such groups containing oxygen, nitrogen or sulfur. Another class of basic corrosion inhibitor comprises oil soluble alkyl amines including decyl amine, undecyl amine, dodecyl amine, tridecyl amine, tetradecyl amine, pentadecyl amine, hexadecyl amine, heptadecyl amine, octadecyl amine, nonadecyl amine, eicosyl amine, etc. Still another class comprises oil soluble alkylene polyamines and particularly N-alkyl alkylene polyamines including N- alkyl propylene diamines in which the alkyl group contains at least 6 and preferably at least 10 carbon atoms. N-alkyl propylene diamines in which the alkyl group is derived from tallow, lauric acid, coconut oil, soya oil, etc., are available commercially at relatively inexpensive prices because they are produced as by-product. For example, Duomeen T is an N-alkyl propylene diamine in which the alkyl group contains from about 12 to about 20 carbon atoms per group and mostly containing 16 to 18 carbon atoms per group. It is understood that a mixture of basic corrosion inhibitors may be employed.
As hereinbefore set forth, the basic corrosion inhibitor retards corrosion of the distillation and connecting cooling, condensing and collecting equipment. The distillate product may comprise t-he overhead fraction withdrawn from the upper portion of the distillation zone as would be the case, for example, when distilling to separate an overhead gasoline fraction from higher boiling material. At the same time or in a separate operation, a fuel oil or lubricating oil fraction may be separated as one or more side cuts. The distillate product, whether an overhead or side out fraction, is subjected to treatment with an alkaline reagent in order to remove acidic components. For example, mercaptans and other acidic components are removed from gasoline by treatment 'with caustic (sodium hydroxide), potassium 'hydroxide, etc., or preferably these in admixture with a solutizing agent including, for example, alcohols, and particularly methanol or ethanol, cresols, tannin, etc., potassium isobutyrate, and others. It is understood that any suitable alkaline treating process may be employed.
As a final step in the treating process, the treated distillate product is separated from the alkaline agent and the distillate product then sent to storage. In accordance with the present invention, an organic acid is comrningled with the treated distillate product on its way to storage or is introduced directly into the storage tank. Any suitable organic acid may be employed and preferably comprises an inexpensive organic acid. A number of relatively inexpensive organic acids are available commercially, these being produced as by-products. One such acid is marketed commercially under the trade name of VR-l Acid. This acid is a liquid at 77 F., has an acid number of about 150, an iodine number of about 36 and is a mixture of polybasic acids, having a titration equivalent weight of about 350. Another inexpensive acid is available commercially under the name of Dimer acid. It is understood that any suitable organic acid may be employed and may be either monobasic or polybasic. It generally is preferred that the acid comprises a long chain carboxylic acid and may be selected from oleic acid, linoleic acid, pa'lmitic acid, stearic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, phthalic acid, etc. As hereinbefore set forth, any suitable organic acid may be used and, when desired, a mixture of organic acids may be employed.
The basic corrosion inhibitor is introduced in the distillation zone in a sufiicient concentration to retard corrosion thereof. The exact amount of inhibitor to be employed will depend upon the corrosive nature of the oil being distilled. In general, the concentration of basic corrosion inhibitor will be within the range of from about '1 to about 15 pounds per 1000 barrels of distillate product, although smaller or larger concentrations may be used. The corrosion inhibitor will be retained to a considerable extent in the distillate product and thereby will serve to retard corrosion of the connecting cooling, condensing and collecting equipment. The organic acid will be used in a concentration sufiicient to form a salt and preferably an acid salt of the basic inhibitor. This will, in turn, depend upon the basic nitrogen content of the basic corrosion inhibitor. For example, in the substituted imidazoline there is one basic nitrogen per molecule. In Duomeen-T there are two basic nitrogens. When a monocarboxylic acid is used, it will be used in equal mol proportions with the substituted imidazoline to form the neutral salt and will be used in a larger concentration and preferably two mols to form the acid salt. On the other hand, when using a dicarboxylic acid with the substituted imidazoline, one mol of acid per two mols of imidazoline will be used to form the neutral salt or equal mols of acid and imidazoline will be used to form the acid salt. When using Duomeen-T, two mols of a monocarboxylic acid salt or one mol of a dicarboxylic acid will be used to form the neutral salt and a larger concentration will be used to form the acid salt. As hereinbefore set forth, the salt will effectively retard corrosion of the storage tank, as well as being retained in part in the distillate product and thereby will provide protection against subsequent metallic equipment through or into which the distillate product is passed.
The following examples are introduced to illustrate further the novelty and utility of the present invention but not with the intention of unduly limiting the same.
Example I It has been established that the ASTM steam turbine oil corrosion test (ASTM Designation D665-52T) correlates with the results obtained in the storage of oil in storage tanks. In this test, a highly polished mild carbon steel rod is placed in 300 cc. of Nujol, to which 30 cc. of synthetic sea water was added, and then heated to and maintained at F. with stirring for 48 hours in a beaker open to the atmosphere;
The basic corrosion inhibitor used in this example ws heptadecylimidazoline and was utilized in a concentration of 0.01% by weight of the Nujol. After heating for 48 hours, corrosion of the steel rod was very heavy; that; is, the rod was completely covered with corrosion. On the other hand, the neutral salt of heptadecyl imidtlZQl nc and VR-l acid (using one mol of acid per two mols of imidazollne), when utilized in a concentration of 0.01% by weight of Nujol and tested in the same manner, resulted in only light corrosion (that is, onetenth or less of the steel rod was covered with rust).
In still another run, the acid salt of heptadecyl imidazoline and VR-l acid (using equal mols of acid and imidazoline), when tested in the same manner as heretofore described, resulted in only slight corrosion of the steel rod. (That is, one-tenth or less of the rod was covered with rust.)
From the above data, it will be noted that the heptadecyl imidazoline is ineffective to retard corrosion of oil in storage tanks. tral salt and the acid salt of heptadecyl imidazoline with VR-l acid were effective in retarding corrosion.
Example 11 In another series of runs similar to those described in Example I, the basic corrosion inhibitor is Duomeen- T. While this compound is eifective in retarding corrosion during distillation of the efiiuent products of thermal cracking, it is not effective in retarding corrosion in the final storage tanks. The Duomeen-T is introduced into the upper portion of the fractionator in a concentration of 7 pounds per 1000 barrels of the overhead fraction withdrawn from the upper portion of the fractionator. The overhead fraction is sent through heat exchangers into a receiver. The Duomeen-T serves to retard corrosion of this equipment. The cracked gasoline then is subjected to treatment with caustic methanol, and the treated gasoline is sent to storage. VR-l acid is commingled with the treated gasoline on its Way to storage in a concentration suflicient to form the acid salt of the Duomeen-T.
I claim as my invention:
1. A method of preventing corrosion of distillation and connecting collecting equipment and of subsequent storage equipment used in the refining of hydrocarbon oil, wherein said oil is subjected to treatment with an alkaline agent between the collecting and storage thereof, which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said collecting equipment is retarded, thereafter subjecting said distillate product to treatment with an alkaline agent selected from the group consisting of sodium hydroxide and potassium hydroxide and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
2. A method of preventing corrosion of distillation and connecting cooling and collecting equipment of a hydrocarbon oil cracking unit and of subsequent storage equipment, which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic cor- On the other hand, both the neurosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt sewing as an inhibitor to retard corrosion of said storage equipment.
3. The process of claim 2 further characterized in that said distillate product is removed as an overhead fraction and comprises gasoline components.
4. The process of claim 2 further characterized in that said distillate product is removed as a side out and comprises components heavier than gasoline.
5. A method of preventing corrosion of distillation and connecting cooling and collecting equipment of a gasoline reforming unit and of subsequent storage equip ment, which comprises distilling the gasoline in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, there after commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration sufiicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
6. A method of preventing corrosion of distillation and connecting cooling and collecting equipment of a crude oil distillation unit and of subsequent storage equipment, which comprises distilling the oil in the presence of a basic corrosion inhibitor which is in part retained in a distillate product of said distillation and selected from the group consisting of an imidazoline, an oil-soluble alkyl amine and an oil-soluble alkylene polyamine, whereby the corrosion of said distillation and of said cooling and collecting equipment is retarded, thereafter subjecting said distillate product to treatment with caustic solution and retaining at least a portion of said basic corrosion inhibitor in said distillate product, thereafter commingling a long chain carboxylic acid with the treated distillate product containing basic corrosion inhibitor in a concentration suflicient to form a salt of the basic corrosion inhibitor, and passing the resultant mixture into storage equipment, said salt serving as an inhibitor to retard corrosion of said storage equipment.
7. The process of claim 6 further characterized in that said distillate product is removed as an overhead fraction and comprises gasoline components.
8. The process of claim 6 further characterized in that said distillate product is removed as a side out and comprises components heavier than gasoline.
9. The method of claim 1 further characterized in that the said basic corrosion inhibitor is an imidazoline.
10. The method of claim 1 further characterized in that the said basic corrosion inhibitor is an N-alkyl propylene diamine in which the alkyl group contains at least 6 carbon atoms.
11. The method of claim 1 further characterized in that the said basic corrosion inhibitor is heptadecyl imidazoline.
References Cited in the file of this patent UNITED STATES PATENTS 2,300,158 Jones Oct. 27, 1942. 2,333,206 Sloan Nov. 2, 1943 2,393,154 Franklin Jan. 15, 1946 2,466,517 Blair et a1. Apr. 5, 1949 2,840,525 Jones June 24, 1958
Claims (1)
1. A METHOD OF PREVENTING CORROSION OF DISTILLATION AND CONNECTING COLLECTING EQUIPMENT AND OF SUBSEQUENT STORAGE EQUIPMENT USED IN THE REFINING OF HYDROCARBON OIL, WHEREIN SAID OIL IS SUBJECTED TO TREATMENT WITH AN ALKALINE AGENT BETWEEN THE COLLECTING AND STORAGE THEREOF, WHICH COMPRISES DISTILLING THE OIL IN THE PRESENCE OF A BASIC CORROSION INHIBITOR WHICH IS IN PART RETAINED IN A DISTILLATE PRODUCT OF SAID DISTILLATION AND SELECTED FROM THE GROUP CONSISTING OF AN IMIDAZOLINE, AN OIL-SOLUBLE ALKYL AMINE AND AN OIL-SOLUBLE ALKYLENE POLYAMINE, WHEREBY THE CORROSION OF SAID DISTILLATION AND OF SAID COLLECTING EQUIPMENT IS RETARDED, THEREAFTER SUBJECTING SAID DISTILLATE PRODUCT TO TREATMENT WITH AN ALKALINE AGENT SELECTED FROM THE GROUP CONSISTING OF SODIUM HYDROXIDE AND POTASSIUM HYDROXIDE AND RETAINING AT LEAST A PORTION OF SAID BASIC CORROSION INHIBITOR IN SAID DISTILLATE PRODUCT, THEREAFTER COMMINGLING A LONG CHAIN CARBOXYLIC ACID WITH THE TREATED DISTILLATE PRODUCT CONTAINING BASIC CORROSION INHIBITOR IN A CONCENTRATION SUFFICIENT TO FORM A SALT OF THE BASIC CORROSION INHIBITOR, AND PASSING THE RESULTANT MIXTURE INTO STORAGE EQUIPMENT, SAID SALT SERVING AS AN INHIBITOR TO RETARD CORROSION OF SAID STORAGE EQUIPMENT.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US534627A US2920030A (en) | 1955-09-15 | 1955-09-15 | Method of preventing corrosion |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US534627A US2920030A (en) | 1955-09-15 | 1955-09-15 | Method of preventing corrosion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2920030A true US2920030A (en) | 1960-01-05 |
Family
ID=24130877
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US534627A Expired - Lifetime US2920030A (en) | 1955-09-15 | 1955-09-15 | Method of preventing corrosion |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2920030A (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3080312A (en) * | 1960-04-13 | 1963-03-05 | Sun Oil Co | Production of lubricating oils from naphthenic crudes |
| US3114702A (en) * | 1960-01-18 | 1963-12-17 | Universal Oil Prod Co | Corrosion inhibition |
| US3247094A (en) * | 1962-11-23 | 1966-04-19 | Nalco Chemical Co | Inhibiting corrosion of metal conductors |
| US3676327A (en) * | 1970-02-19 | 1972-07-11 | Exxon Research Engineering Co | Inhibition of corrosion by hydrotreater effluent |
| US3819328A (en) * | 1970-06-24 | 1974-06-25 | Petrolite Corp | Use of alkylene polyamines in distillation columns to control corrosion |
| US4486299A (en) * | 1982-09-10 | 1984-12-04 | Phillips Petroleum Company | Removing NH3 and H2 S from aqueous streams |
| US4855035A (en) * | 1988-09-14 | 1989-08-08 | Shell Oil Company | Method of abating corrosion in crude oil distillation units |
| US11015135B2 (en) | 2016-08-25 | 2021-05-25 | Bl Technologies, Inc. | Reduced fouling of hydrocarbon oil |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2300158A (en) * | 1940-10-18 | 1942-10-27 | Standard Oil Dev Co | Refining mineral oil |
| US2333206A (en) * | 1939-05-13 | 1943-11-02 | Du Pont | Protection of ferrous metals against corrosion |
| US2393154A (en) * | 1942-07-28 | 1946-01-15 | Standard Oil Dev Co | Petroleum products |
| US2466517A (en) * | 1948-01-10 | 1949-04-05 | Petrolite Corp | Processes for preventing corrosion and corrosion inhibitors |
| US2840525A (en) * | 1953-10-01 | 1958-06-24 | Pan American Petroleum Corp | Method of inhibiting corrosion of metal surfaces |
-
1955
- 1955-09-15 US US534627A patent/US2920030A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2333206A (en) * | 1939-05-13 | 1943-11-02 | Du Pont | Protection of ferrous metals against corrosion |
| US2300158A (en) * | 1940-10-18 | 1942-10-27 | Standard Oil Dev Co | Refining mineral oil |
| US2393154A (en) * | 1942-07-28 | 1946-01-15 | Standard Oil Dev Co | Petroleum products |
| US2466517A (en) * | 1948-01-10 | 1949-04-05 | Petrolite Corp | Processes for preventing corrosion and corrosion inhibitors |
| US2840525A (en) * | 1953-10-01 | 1958-06-24 | Pan American Petroleum Corp | Method of inhibiting corrosion of metal surfaces |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3114702A (en) * | 1960-01-18 | 1963-12-17 | Universal Oil Prod Co | Corrosion inhibition |
| US3080312A (en) * | 1960-04-13 | 1963-03-05 | Sun Oil Co | Production of lubricating oils from naphthenic crudes |
| US3247094A (en) * | 1962-11-23 | 1966-04-19 | Nalco Chemical Co | Inhibiting corrosion of metal conductors |
| US3676327A (en) * | 1970-02-19 | 1972-07-11 | Exxon Research Engineering Co | Inhibition of corrosion by hydrotreater effluent |
| US3819328A (en) * | 1970-06-24 | 1974-06-25 | Petrolite Corp | Use of alkylene polyamines in distillation columns to control corrosion |
| US4486299A (en) * | 1982-09-10 | 1984-12-04 | Phillips Petroleum Company | Removing NH3 and H2 S from aqueous streams |
| US4855035A (en) * | 1988-09-14 | 1989-08-08 | Shell Oil Company | Method of abating corrosion in crude oil distillation units |
| US11015135B2 (en) | 2016-08-25 | 2021-05-25 | Bl Technologies, Inc. | Reduced fouling of hydrocarbon oil |
| US12031096B2 (en) | 2016-08-25 | 2024-07-09 | Bl Technologies, Inc. | Reduced fouling of hydrocarbon oil |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4062764A (en) | Method for neutralizing acidic components in petroleum refining units using an alkoxyalkylamine | |
| US2638450A (en) | Reaction products of nu-alkylated polyalkylenepolyamines and alkenyl succinic acid anhydrides | |
| US2668100A (en) | Corrosion inhibitor for liquid hydrocarbons | |
| US2830019A (en) | Additive for mineral oil | |
| US4344861A (en) | Bis-amides as corrosion inhibitors | |
| US3447891A (en) | Corrosion inhibiting process | |
| US3705109A (en) | Corrosion inhibiting composition and use thereof | |
| US2920030A (en) | Method of preventing corrosion | |
| US3458453A (en) | Corrosion inhibiting composition containing a neutral amide and c3-c8 volatile amine | |
| US3123634A (en) | Chzchsocchzchzcoh | |
| US3997469A (en) | Corrosion inhibition with oil soluble diamides | |
| US3696048A (en) | Corrosion inhibiting composition and use thereof | |
| US2907646A (en) | Rust inhibitor for fuel fractions of mineral oil | |
| US2944969A (en) | Prevention of rust and corrosion | |
| US3790496A (en) | Alkylene polyamine polymeric reaction product corrosion inhibitor | |
| US3060007A (en) | Hydrocarbon oils containing reaction products of imidazolines and alkylene iminodiacetic acids | |
| US4752381A (en) | Upgrading petroleum and petroleum fractions | |
| US3247110A (en) | Fuel oil and lubricating oil compositions containing metal salts of the mono-amidesof tetrapropenyl succinic acid | |
| US2948598A (en) | Anti-rust compositions | |
| US3061553A (en) | Corrosion inhibitors | |
| US2863746A (en) | Aviation grade gasolines containing n-alkyl amine salts of dialkyl acid orthophosphates | |
| US3017357A (en) | Hydrocarbon oil composition | |
| US2941943A (en) | Method of inhibiting corrosion | |
| US3114702A (en) | Corrosion inhibition | |
| US2935389A (en) | Rust inhibited mineral oil compositions |