US2836564A - Corrosion inhibitors and compositions containing the same - Google Patents

Corrosion inhibitors and compositions containing the same Download PDF

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US2836564A
US2836564A US465438A US46543854A US2836564A US 2836564 A US2836564 A US 2836564A US 465438 A US465438 A US 465438A US 46543854 A US46543854 A US 46543854A US 2836564 A US2836564 A US 2836564A
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oils
oil
rusting
corrosion
acid
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US465438A
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Edward N Roberts
Ellis K Fields
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Standard Oil Co
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Standard Oil Co
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D285/00Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
    • C07D285/01Five-membered rings
    • C07D285/02Thiadiazoles; Hydrogenated thiadiazoles
    • C07D285/04Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
    • C07D285/121,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
    • C07D285/1251,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/24Organic compounds containing sulfur, selenium and/or tellurium
    • C10L1/2443Organic compounds containing sulfur, selenium and/or tellurium heterocyclic compounds
    • C10L1/2456Organic compounds containing sulfur, selenium and/or tellurium heterocyclic compounds sulfur with oxygen and/or nitrogen in the ring, e.g. thiazoles
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M1/00Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
    • C10M1/08Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
    • CCHEMISTRY; METALLURGY
    • C23COATING 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
    • C23FNON-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
    • C23F11/00Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
    • C23F11/08Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
    • C23F11/10Inhibiting 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
    • C23F11/16Sulfur-containing compounds
    • C23F11/165Heterocyclic compounds containing sulfur as hetero atom
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2201/00Inorganic compounds or elements as ingredients in lubricant compositions
    • C10M2201/02Water
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/023Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/025Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with condensed rings
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2215/00Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
    • C10M2215/02Amines, e.g. polyalkylene polyamines; Quaternary amines
    • C10M2215/06Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
    • C10M2215/064Di- and triaryl amines
    • C10M2215/065Phenyl-Naphthyl amines
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    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/04Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
    • C10M2219/044Sulfonic acids, Derivatives thereof, e.g. neutral salts
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/102Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/10Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
    • C10M2219/104Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
    • C10M2219/106Thiadiazoles
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/12Inhibition of corrosion, e.g. anti-rust agents or anti-corrosives
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/044Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for manual transmissions
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    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/04Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/046Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for traction drives
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/08Hydraulic fluids, e.g. brake-fluids
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/135Steam engines or turbines
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/16Dielectric; Insulating oil or insulators
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/14Electric or magnetic purposes
    • C10N2040/17Electric or magnetic purposes for electric contacts
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    • C10N2040/00Specified use or application for which the lubricating composition is intended
    • C10N2040/20Metal working
    • C10N2040/22Metal working with essential removal of material, e.g. cutting, grinding or drilling
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    • C10N2040/46Textile oils
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    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • This invention is directed to condensation products of alpha-halogenated aliphatic mono-carboxylic acids and 2,5-dimercapto-1,3,4-thiadiazole as new compositions of matter, and to-compositions containing the same, which compositions possess corrosion and/or rust inhibiting properties.
  • The'pr esent invention is also applicable to anti-rust or slushing compositions for the protection'of metals against atmospheric corrosion and/or rusting.
  • anti-rust or slushing compositions are applied to metallic articles to be stored or for shipment to prevent rusting and/or corrosion thereof.
  • fabricated metallic articles and finished or semi-finished metal stocks destined for shipment-by rail or by water are protected against attack by moisture by coating such materials with anti-rust or slushing compositions.
  • Another object of the invention is to provide a composition which will effectively inhibit or prevent the rusting and/or corrosion of metallic surfaces which come in contact with water and/or steam.
  • Still another object of the invention is to provide a .slushing composition whichwill' prevent or inhibit the rusting and/or corrosion of metal surfaces.
  • Such compounds can be named as 1,3,4-thiadiazole-Z,S-bis-(thia-alpha-aliphatic acids) or 1,3,4-thiadiazo1e-2,5-bis-(alpha-mercapto-aliphatic acids).
  • condensation products can be readily prepared by refluxing for a period of 3 to 4 hours a mixture of one mole of an alkali metal salt of 2,5-dimercapto-1,3,4-
  • the product acid set free as an oil, was extracted with hexane and the hexane extract washed once with water and then Thehexane solution was then dried with 20% ehtanol. over sodium sulfate, filtered and freed of hexane by evaporation. tion yielded a light buff colored solid having a melting point of 81 C.
  • condensation products find particular utility in oleaginous compositions to impart corrosion and/or rust inhibiting properties thereto.
  • condensation product described herein can be suitably employed in oleaginous compositions in general, particularly to inhibit or prevent rusting and/ or corrosion, for the purpose of exemplifying the present invention the same will be described as applied to steam turbine lubricants for which highly refined oils having Saybolt Universal viscosities at 100 F. of from about 100 seconds to about 250 seconds are usually employed.
  • condensation products are especially well adapted for use in turbine oil compositions they can be used in small proportions, namely from about 0.001% to about 1% in a wide variety of oleaginous bases such as by Way of illustration, hydrocarbon oils, i. e. petroleum oils and synthetic hydrocarbon oils, aliphatic dicarboxylic acid esters, silicone polymers, 1,2 polyoxypropylene aliphatic ethers such as described in U. S. 2,488,644, esters'of dihydroxy thioethers such as described in U. S. 2,451,895, and other oleaginous compounds.
  • hydrocarbon oils i. e. petroleum oils and synthetic hydrocarbon oils
  • aliphatic dicarboxylic acid esters aliphatic dicarboxylic acid esters
  • silicone polymers 1,2 polyoxypropylene aliphatic ethers
  • 1,2 polyoxypropylene aliphatic ethers such as described in U. S. 2,488,644, esters'of dihydroxy thioethers such as described
  • Motor fuels for example, automobile or aviation gasolines, tractor fuels, diesel engine fuels, alcohol-containing motor fuels;
  • Solvent naphthas such as Stoddard solvent, V. M. and P. naphthas, hydroformed naphthas;
  • Lubricating and dielectric oils motor oils, diesel oils,
  • oil field machinery lubricants ice-machine oils, ste'arn cylinder lubricants, transmission oils, soluble oils, textile oils, cutting oils, turbine oils, insulating oils;
  • Lubricating greases stable gel-like or solid dispersions of metal soaps in hydrocarbon oils
  • compositions can in addition contain V. I. improvers, viscosity-increasing agents, bloom producing agents, extreme pressure agents, anti-oxidants, dyes, and anti-knock agents, as well as other rust or corrosion inhibiting agents such as, oil-soluble alkali metal sulfonates, for example sodium mahogany soap, etc., provided only that these additional agents do not enter into appreciable chemical reaction with the described condensation products or precipitate them from the oils to which they have been added.
  • V. I. improvers, viscosity-increasing agents, bloom producing agents, extreme pressure agents, anti-oxidants, dyes, and anti-knock agents as well as other rust or corrosion inhibiting agents such as, oil-soluble alkali metal sulfonates, for example sodium mahogany soap, etc.
  • an antioxidant such as the polyhydric phenols and their alkyl derivatives, for example, catechol, tertiary butyl catechol, octyl catechol, etc.
  • the antioxidant may suitably be used in a pro- While the present invention has been described by reference to specific embodiments thereof, these are given by way of illustration only and the invention is not to be limited thereto, but includes within its scope such modifications and variations as come within the spirit of the appended claims.
  • a lubricant composition comprising a major propor- 6.
  • a lubricant composition comprising a major proportion of a hydrocarbon oirl and from about 0.001% to about 1% 1,3,4-thiadiazole-2,5-bis-(thia-alpha-lauric acid).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Lubricants (AREA)

Description

" Uni d Edward N. Roberts, Los Altos, Calm, and Ellis K. Fields,
, Chicago, Ill., assignors to Standard Oil Company, Chicago, 111., a corporation of Indiana No Drawing. Application October 28, 1954 Serial No. 465,438
6 claims. (or. 25247.5
This invention is directed to condensation products of alpha-halogenated aliphatic mono-carboxylic acids and 2,5-dimercapto-1,3,4-thiadiazole as new compositions of matter, and to-compositions containing the same, which compositions possess corrosion and/or rust inhibiting properties.
In various equipment in which water and/or steam is used, or which may become contaminated with water or steam during service or storage, corrosion and/or rusting of the metal parts, particularly the ferrous metal parts, is encountered causing material damage to such equipment. For example, in the operation of steam turbines, rusting or corrosion of the metal parts of such systems is a serious problem, and hence, prevention or inhibition of such corrosion or rusting is highly important. Similar problems exist in the lubrication of certain types of marine engines.
The'pr esent invention is also applicable to anti-rust or slushing compositions for the protection'of metals against atmospheric corrosion and/or rusting. Such anti-rust or slushing compositions are applied to metallic articles to be stored or for shipment to prevent rusting and/or corrosion thereof. Similarly, fabricated metallic articles and finished or semi-finished metal stocks destined for shipment-by rail or by water are protected against attack by moisture by coating such materials with anti-rust or slushing compositions.
Accordingly, it is an object of the present invention to provide a composition which will effectively inhibit orprevent the rusting and/ or corrosion of metallic surfaces.
Another object of the invention is to provide a composition which will effectively inhibit or prevent the rusting and/or corrosion of metallic surfaces which come in contact with water and/or steam.
A further object of the invention is to provide a turbine oil which will effectively inhibit the rusting and corrosion of the metal surfaces of the system which come in contactwith water or steam. Still another object of the invention is to provide alubricant composition whichwill effectively inhibit or prevent the corrosion and/or rusting of metal surfaces" of equipment employing such lubricant, particularly in equipment in which steam or water may be present. a
4 Still another object of the invention is to provide a .slushing composition whichwill' prevent or inhibit the rusting and/or corrosion of metal surfaces.
The new compositions of matter, o f the present invenf tion are the condensation products ofan ;a1pha halo ice 25 carbon atoms, with 2,5-dimercapto-1,3,4-thiadiazole, which condensation product has the general formula B and a d... (i=3; s =0 on n in which R is an alkyl radical of at least about 10 carbon atoms and preferably from about:l2 to about 25 carbon atoms. Such compounds can be named as 1,3,4-thiadiazole-Z,S-bis-(thia-alpha-aliphatic acids) or 1,3,4-thiadiazo1e-2,5-bis-(alpha-mercapto-aliphatic acids).
These condensation products can be readily prepared by refluxing for a period of 3 to 4 hours a mixture of one mole of an alkali metal salt of 2,5-dimercapto-1,3,4-
thiadiazole and two moles of an alkali metal salt of the alpha-halogenated-aliphatic mono-carboxylic acid, decomposing the resultant salt of the condensation product with an excess of a mineral acid, for example, HCl, and extracting the free acid with a suitable organic solvent such as hexane, naphtha, and washing .the hexane solution free of the mineral acid with water or a dilute aqueous alcohol solution. The organic solvent solution is then dried and the organic acid recovered by removal 'of the organic solvent by suitable means such as by Example I Fifteen grams (0.1 mole) of 2,5-dimercapto-l,3,4-
thiadiazole in cc. ethanol was treated with 12.8 grams (0.2 mole) of KOH (87.9%) dissolved in 90 cc. ethanol. To the cooled suspension-solution were added 72.7 grams (0.2 mole) of alpha-brom-stearic acid and 11.2 grams KOH dissolved in cc. ethanol with an additional 90 .cc. ehtanol. on a steam bath and refluxed for '4 hours. The mixture was then diluted with about an equal volume of Water and treated with an excess of concentrated HCl. The product acid, set free as an oil, was extracted with hexane and the hexane extract washed once with water and then Thehexane solution was then dried with 20% ehtanol. over sodium sulfate, filtered and freed of hexane by evaporation. tion yielded a light buff colored solid having a melting point of 81 C.
The mixture was stirred and warmed Recrystallization from a benzene-hexane solu- Forty-five grams (03 mole) of '2,5-dimercapto-l,3,4- thiadiazole in 300 cc. ethanol were treated with 33.6 grams (0.6 mole) of KOH in 150 cc. ethanol. To the cooled mixture were added 155.4 grams (0.6 mole) of alphabrom-lauric acid and 33.6 grams KOH in 200 cc. ethanol and the mixture refiuxed on a steam bath for 3 hours. The mixture was then acidified with 65 cc. concentrated I-lCl and the acid separated from the salt by filtration. The filtrate Was evaporated under vacuum, and taken up in 250 cc. hexane, dried over Drierite, filtered and the hexane evaporated off. The recovered waxy solid was purified by crystallization from heptane. A solid having "a melting point of 86-87 C., and the following analysis was obtained:
The herein described condensation products find particular utility in oleaginous compositions to impart corrosion and/or rust inhibiting properties thereto. Although the condensation product described herein can be suitably employed in oleaginous compositions in general, particularly to inhibit or prevent rusting and/ or corrosion, for the purpose of exemplifying the present invention the same will be described as applied to steam turbine lubricants for which highly refined oils having Saybolt Universal viscosities at 100 F. of from about 100 seconds to about 250 seconds are usually employed.
With the advent of drastic refining treatments to produce more highly refined turbine oils having improved non-sludging and emulsification properties, certain components of such oils, responsible for the wetting and therefore rust inhibiting properties of the oil are, however, removed. As a result, such oxidation-stable oils, produced by the drastic refining treatments, are inferior with respect to rust inhibiting qualities. Rusting in steam turbine systems is usually encountered in the upper portions of the oil reservoirs and other parts of the systems by virtue of droplets of water coming in contact with the metallic surfaces and displacing any oil which may be present thereon. Oil will provide adequate protection against such rusting only if it wets the metal surfaces preferentially as compared with water. As the rusting in steam turbine systems progresses the iron oxides formed may scale olT and be carried in suspension in the oil; often scoring bearings, plugging oil lines and frequently causing faulty operation of delicate governor parts. The need for non-rusting turbine oils is therefore great.
In accordance with one embodiment of the present invention the addition of small amounts of a condensation product of the type herein described to turbine oils effectively inhibits rusting of the type above described. The rust inhibiting characteristic of turbine oils containing such additives is demonstrated by the following test:
Three hundred cubic centimeters of the oil to be tested are placed in a 400 cc. lipless glass beaker and heated 'to 140 F. in an oil bathand the oil stirred with a stirrer maintained at about 1000 R. P. M. When the temperature of the oil sample reaches 140 F. a cleaned strip of cold rolled steel is suspended in the oil and the stirring continued for 30 minutes to insure complete wetting of the steel specimen. Thirty cubic centimeters of distilled water are then carefully added by pouring it down the side of the beaker, and stirring continued for 24 hours. At
the presence of rust. The method of carrying out this Additive Weight Degree of percent Rusting None (control) Severe rust. Product of Example I 0.1 No rust.
Do. 0. 05 0. Do 0. O3 Slfghtrust. Do 0.01 No rust. Product of Example II 0. 1 Do. Do. O. 03 Do. Do 0.01 Do. Do. 0.001 Do.
While the herein described condensation products are especially well adapted for use in turbine oil compositions they can be used in small proportions, namely from about 0.001% to about 1% in a wide variety of oleaginous bases such as by Way of illustration, hydrocarbon oils, i. e. petroleum oils and synthetic hydrocarbon oils, aliphatic dicarboxylic acid esters, silicone polymers, 1,2 polyoxypropylene aliphatic ethers such as described in U. S. 2,488,644, esters'of dihydroxy thioethers such as described in U. S. 2,451,895, and other oleaginous compounds. Illustrative of the media in which these additives can be employed are the following:
Motor fuels; for example, automobile or aviation gasolines, tractor fuels, diesel engine fuels, alcohol-containing motor fuels;
Lighting and heating fuels; kerosene stove oils, stove and lighting naphthas, furnace oils, fuels;
Solvent naphthas, cleaner naphthas, such as Stoddard solvent, V. M. and P. naphthas, hydroformed naphthas;
Lubricating and dielectric oils; motor oils, diesel oils,
aviation engine oils, marine engine lubricants, gear oils,
oil field machinery lubricants, ice-machine oils, ste'arn cylinder lubricants, transmission oils, soluble oils, textile oils, cutting oils, turbine oils, insulating oils;
Lubricating greases; stable gel-like or solid dispersions of metal soaps in hydrocarbon oils;
Protective coatings; 'slushing oils and greases in which part or all of the hydrocarbon oil may be replaced by metal soaps, pitches, tars, asphalt, rosin, parafiin wax,
etc.
The herein described compositions can in addition contain V. I. improvers, viscosity-increasing agents, bloom producing agents, extreme pressure agents, anti-oxidants, dyes, and anti-knock agents, as well as other rust or corrosion inhibiting agents such as, oil-soluble alkali metal sulfonates, for example sodium mahogany soap, etc., provided only that these additional agents do not enter into appreciable chemical reaction with the described condensation products or precipitate them from the oils to which they have been added.
Thus, in turbine oils, we can in addition to the described condensation products, add an antioxidant such as the polyhydric phenols and their alkyl derivatives, for example, catechol, tertiary butyl catechol, octyl catechol, etc. Other eflfective antioxidants include beta-naphthol, amyl beta-naphthol, =octyl beta-naphthol, lauryl betanaphthol, alpha-naphthol, amyl alpha-naphth'ol, N-phenyl alph'a-naphthyl-amine, di-alpha-naphthyl-amin'e and the like. portion in the range'of about 0.001% to about 0.25% (by weight) based on the oil.
Percentages given herein and in 'the appended --'claims are weight percentages unless otherwise stated.
The antioxidant may suitably be used in a pro- While the present invention has been described by reference to specific embodiments thereof, these are given by way of illustration only and the invention is not to be limited thereto, but includes within its scope such modifications and variations as come within the spirit of the appended claims.
We claim:
1. As a new compound a 1,3,4-thiadiazole-2,5-bis-(thiaalpha-aliphatic acid) having the general formula in which R is an alkyl radical of from about 10 to about 25 carbon atoms.
2. The compound, 1,3,4-thiadiazole-2,5-bis-(thia-alphalauric acid).
3. The compound 1,3,4-thiadiazole-2,5-bis-(thia-alphastearic acid).
4. A lubricant composition comprising a major propor- 6. A lubricant composition comprising a major proportion of a hydrocarbon oirl and from about 0.001% to about 1% 1,3,4-thiadiazole-2,5-bis-(thia-alpha-lauric acid).
References Cited in the file of this patent UNITED STATES PATENTS 2,690,999 Lowe et a1. Oct. 5, 1954 2,736,729 Krzikalla Feb. 28, 1956

Claims (1)

  1. 4. A LUBRICANT COMPOSITION COMPRISING A MAJOR PROPORTION OF A HYDROCARBON OIL AND FROM ABOUT 0.001% TO ABOUT 1% OF A COMPOUND HAVING THE GENERAL FORMULA
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Cited By (42)

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US3040054A (en) * 1960-08-03 1962-06-19 Olin Mathieson 2, 2'-(1, 4-diaminotetramethylene) bis(4-thiazolecarboxylic acid), salts and process
US3376224A (en) * 1963-05-24 1968-04-02 Castrol Ltd Lubricating compositions and antioxidants therefor
US3519564A (en) * 1967-08-25 1970-07-07 Lubrizol Corp Heterocyclic nitrogen-sulfur compositions and lubricants containing them
US3609079A (en) * 1968-12-13 1971-09-28 Martin J Devine Silicone lubricants
US4193882A (en) * 1973-07-06 1980-03-18 Mobil Oil Corporation Corrosion inhibited lubricant composition
US4210544A (en) * 1976-08-18 1980-07-01 Texaco Inc. Dual purpose cutting oil composition
US4301019A (en) * 1980-10-29 1981-11-17 Mobil Oil Corporation Mercaptothiadiazole adducts of unsaturated esters and lubricants containing same
US4382869A (en) * 1981-06-18 1983-05-10 Mobil Oil Corporation Friction reducing and corrosion inhibiting lubricant additives and their compositions
US4584114A (en) * 1980-12-19 1986-04-22 Mobil Oil Corporation Multifunctional lubricant additives and compositions thereof
WO1986004601A1 (en) 1985-01-31 1986-08-14 The Lubrizol Corporation Sulfur-containing compositions, and additive concentrates and lubricating oils containing same
EP0218816A1 (en) * 1985-10-15 1987-04-22 Pennwalt Corporation Thiadiazole compounds and lubricant additives thereof
EP0223916A1 (en) * 1985-10-03 1987-06-03 ATOCHEM NORTH AMERICA, INC. (a Pennsylvania corp.) Multifunctional thiadiazole lubricant additives
EP0320450A1 (en) * 1987-12-08 1989-06-14 Ciba-Geigy Ag Lubricant composition containing multifunctional lubricant additives
EP0398843A1 (en) * 1989-05-17 1990-11-22 Ciba-Geigy Ag Lubricant compositions
US4990652A (en) * 1985-10-03 1991-02-05 Atochem North America, Inc. Intermediates for preparing multifunctional thiadiazole lubricant additives
US5102568A (en) * 1985-10-15 1992-04-07 Atochem North America, Inc. Thiadiazole compounds and lubricant additives thereof
WO1992007841A1 (en) * 1990-11-01 1992-05-14 Mobil Oil Corporation Antiwear/antioxidant additives based on dimercapto derivatives of acrylates and methacrylates polymers and amine reaction products thereof
US5177213A (en) * 1989-07-20 1993-01-05 R. T. Vanderbilt Company, Inc. Succinate derivatives of 2,5-dimercapto-1,3,4-thiadiazoles
EP0289964B1 (en) * 1987-05-04 1993-07-28 R.T. Vanderbilt Company, Inc. Maleic acid derivatives of 2,5-dimercapto-1,3,4-thiadiazoles and lubricating compositions containing same
US5318712A (en) * 1992-10-13 1994-06-07 The Lubrizol Corporation Lubricants, greases, aqueous fluids and concentrates containing additives derived from dimercaptothiadiazoles
US5320764A (en) * 1991-07-17 1994-06-14 Ciba-Geigy Corporation Multifunctional lubricant additives
US5368758A (en) * 1992-10-13 1994-11-29 The Lubrizol Corporation Lubricants, greases and aqueous fluids containing additives derived from dimercaptothiadiazoles
US5585029A (en) * 1995-12-22 1996-12-17 Exxon Research And Engineering Company High load-carrying turbo oils containing amine phosphate and 2-alkylthio-1,3,4-thiadiazole-5-alkanoic acid
US5801130A (en) * 1995-12-22 1998-09-01 Exxon Research And Engineering Company High load-carrying turbo oils containing amine phosphate and dimercaptothiadiazole derivatives
US6573223B1 (en) 2002-03-04 2003-06-03 The Lubrizol Corporation Lubricating compositions with good thermal stability and demulsibility properties
WO2015142633A1 (en) 2014-03-18 2015-09-24 Baker Hughes Incorporated Dimercaptothiadiazoles to prevent corrosion of mild steel by acid gases in oil and gas products
DE102015118989A1 (en) 2014-11-05 2016-05-12 Infineum International Ltd. Power transmission fluids with improved material compatibility
WO2016164345A1 (en) 2015-04-09 2016-10-13 The Lubrizol Corporation Lubricants containing quaternary ammonium compounds
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US2736729A (en) * 1953-08-20 1956-02-28 Basf Ag Substitution products of 1,3,4-thiadiazole and process

Cited By (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3040054A (en) * 1960-08-03 1962-06-19 Olin Mathieson 2, 2'-(1, 4-diaminotetramethylene) bis(4-thiazolecarboxylic acid), salts and process
US3376224A (en) * 1963-05-24 1968-04-02 Castrol Ltd Lubricating compositions and antioxidants therefor
US3519564A (en) * 1967-08-25 1970-07-07 Lubrizol Corp Heterocyclic nitrogen-sulfur compositions and lubricants containing them
US3609079A (en) * 1968-12-13 1971-09-28 Martin J Devine Silicone lubricants
US4193882A (en) * 1973-07-06 1980-03-18 Mobil Oil Corporation Corrosion inhibited lubricant composition
US4210544A (en) * 1976-08-18 1980-07-01 Texaco Inc. Dual purpose cutting oil composition
US4301019A (en) * 1980-10-29 1981-11-17 Mobil Oil Corporation Mercaptothiadiazole adducts of unsaturated esters and lubricants containing same
US4584114A (en) * 1980-12-19 1986-04-22 Mobil Oil Corporation Multifunctional lubricant additives and compositions thereof
US4382869A (en) * 1981-06-18 1983-05-10 Mobil Oil Corporation Friction reducing and corrosion inhibiting lubricant additives and their compositions
WO1986004601A1 (en) 1985-01-31 1986-08-14 The Lubrizol Corporation Sulfur-containing compositions, and additive concentrates and lubricating oils containing same
EP0223916A1 (en) * 1985-10-03 1987-06-03 ATOCHEM NORTH AMERICA, INC. (a Pennsylvania corp.) Multifunctional thiadiazole lubricant additives
US4990652A (en) * 1985-10-03 1991-02-05 Atochem North America, Inc. Intermediates for preparing multifunctional thiadiazole lubricant additives
US4902804A (en) * 1985-10-03 1990-02-20 Pennwalt Corporation Multifunctional thiadiazole lubricant additives
EP0218816A1 (en) * 1985-10-15 1987-04-22 Pennwalt Corporation Thiadiazole compounds and lubricant additives thereof
WO1987002358A1 (en) * 1985-10-15 1987-04-23 Pennwalt Corporation Thiadiazole compounds and lubricant additives thereof
US5102568A (en) * 1985-10-15 1992-04-07 Atochem North America, Inc. Thiadiazole compounds and lubricant additives thereof
EP0289964B1 (en) * 1987-05-04 1993-07-28 R.T. Vanderbilt Company, Inc. Maleic acid derivatives of 2,5-dimercapto-1,3,4-thiadiazoles and lubricating compositions containing same
US4931196A (en) * 1987-12-08 1990-06-05 Ciba-Geigy Corporation Lubricant composition containing multifunctional lubricant additives
EP0320450A1 (en) * 1987-12-08 1989-06-14 Ciba-Geigy Ag Lubricant composition containing multifunctional lubricant additives
EP0398843A1 (en) * 1989-05-17 1990-11-22 Ciba-Geigy Ag Lubricant compositions
US5037568A (en) * 1989-05-17 1991-08-06 Ciba-Geigy Corporation Lubricant compositions
US5177213A (en) * 1989-07-20 1993-01-05 R. T. Vanderbilt Company, Inc. Succinate derivatives of 2,5-dimercapto-1,3,4-thiadiazoles
WO1992007841A1 (en) * 1990-11-01 1992-05-14 Mobil Oil Corporation Antiwear/antioxidant additives based on dimercapto derivatives of acrylates and methacrylates polymers and amine reaction products thereof
US5188746A (en) * 1990-11-01 1993-02-23 Mobil Oil Corporation Antiwear/antioxidant additives based on dimercapto derivatives of acrylates and methacrylates polymers and amine reaction products thereof
US5320764A (en) * 1991-07-17 1994-06-14 Ciba-Geigy Corporation Multifunctional lubricant additives
US5318712A (en) * 1992-10-13 1994-06-07 The Lubrizol Corporation Lubricants, greases, aqueous fluids and concentrates containing additives derived from dimercaptothiadiazoles
US5368758A (en) * 1992-10-13 1994-11-29 The Lubrizol Corporation Lubricants, greases and aqueous fluids containing additives derived from dimercaptothiadiazoles
EP0780461A1 (en) 1995-12-22 1997-06-25 Exxon Research And Engineering Company High load-carrying turbo oils containing amine phoshate and 2-alkylthio-1,3,4-thiadiazole-5-alkanoic acid
US5801130A (en) * 1995-12-22 1998-09-01 Exxon Research And Engineering Company High load-carrying turbo oils containing amine phosphate and dimercaptothiadiazole derivatives
US5585029A (en) * 1995-12-22 1996-12-17 Exxon Research And Engineering Company High load-carrying turbo oils containing amine phosphate and 2-alkylthio-1,3,4-thiadiazole-5-alkanoic acid
US6573223B1 (en) 2002-03-04 2003-06-03 The Lubrizol Corporation Lubricating compositions with good thermal stability and demulsibility properties
EP3119925A4 (en) * 2014-03-18 2017-11-22 Baker Hughes Incorporated Dimercaptothiadiazoles to prevent corrosion of mild steel by acid gases in oil and gas products
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