US2648643A - Engine corrosion preventive - Google Patents

Engine corrosion preventive Download PDF

Info

Publication number
US2648643A
US2648643A US169516A US16951650A US2648643A US 2648643 A US2648643 A US 2648643A US 169516 A US169516 A US 169516A US 16951650 A US16951650 A US 16951650A US 2648643 A US2648643 A US 2648643A
Authority
US
United States
Prior art keywords
parts
wax
corrosion
oil
weight
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
Application number
US169516A
Inventor
Adams William Henry
Ervine William Denis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Application granted granted Critical
Publication of US2648643A publication Critical patent/US2648643A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • 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
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2201/08Inorganic acids or salts thereof
    • C10M2201/082Inorganic acids or salts thereof containing nitrogen
    • C10M2201/083Inorganic acids or salts thereof containing nitrogen nitrites
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/026Butene
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/06Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing conjugated dienes
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/14Synthetic waxes, e.g. polythene waxes
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/16Paraffin waxes; Petrolatum, e.g. slack wax
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/17Fisher Tropsch reaction products
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2205/00Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/22Alkylation reaction products with aromatic type compounds, e.g. Friedel-crafts
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/08Amides
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/08Amides
    • C10M2215/082Amides containing hydroxyl groups; Alkoxylated derivatives
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2215/28Amides; Imides
    • CCHEMISTRY; METALLURGY
    • 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
    • C10M2219/04Organic 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • 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
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015Dispersions of solid lubricants
    • C10N2050/02Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Semi-solids; greasy

Definitions

  • the present invention relates to improved corrosion preventive compositions which may be applied to metal surfaces, especially ferrous metal surfaces, to form protective coatings.
  • the invention is particularly concerned with the production of wax-containing compositions which have good adhesion properties when applied to metal surfaces.
  • the waxy film After evaporation of the volatile solvent, the waxy film should form a protective coating over the Whole of the exposed metal surface, but it has been found that the film frequently cracks and even, in some cases, slips bodily over the surface exposing part of it to corrosion.
  • the structure of the wax coating may be modified by the addition to the wax of minor proportions of well known types of pour point depressor which are conventionally used with lubricating oils, together with a high molecular Weight polyiso-olefin.
  • the effects of these wax modifiers are such that the adherence of the coating to the metal is greatly'
  • the pour point depressor is preferably a Friedel- Crafts condensation product of the halogenated long-chain hydrocarbon and aromatic type, e. g. a chlorinated parafiin Wax and naphthalene but other known and generally equivalent pour point depressors such as chlorinated wax-phenol compounds may be used.
  • the polyiso-olefin to be used may be any C3 to C14 iso-olefin polymer having a molecular weight between 20,000 and 200,000 but is preferably a polyisobutylene and preferably has a molecular weight between 40,000 and 100,000.
  • the copolymers of similar properties such as Butyl rubber, which is a copolymer predominantly of isobutylene with small proportions of a multiolefin such as isoprene, may be used for the same purposes.
  • the wax-containing corrosion preventive may comprise essentially a de-oiled petrolatum wax, i. e., a microcrystalline petroleum wax, a volatile solvent in which the wax is sparingly soluble at room temperature and readily soluble when hot, a lubricating oi1 and, usually but not always necessarily, minor proportions of conventional corrosion inhibitors.
  • the composition may be prepared by melting the wax together with the pour point depressor, the polyiso-olefin, the lubricating oil and corrosion inhibitors, dissolving this mixture in the moderately heated volatile solvent and chilling the solution rapidly and with agitation. This allows the formation of a suspension of microcrystalline wax of very fine particle size having a good degree of stability.
  • the wax used should preferably be a hard deoiled petroleum wax such as a mi-crocrystalline petroleum wax having a melting point in the range to 210 F. and one having a melting point between 180 and 200 F; is preferred.
  • the solvent may be any volatile solvent boiling, for example, in the range 40 to C. and in which the wax is sparingly soluble at room temperature and readily soluble at higher temperatures but it is preferred that a hydrocarbon solvent be used and it is most convenient that the solvent chosen should have a boiling range between 70 and 120 C.
  • Examples of conventional corrosion inhibitors are the alkali-metal and alkaline earth metal oilsoluble petroleum sulphonates, particularly sodium petroleum sulphon'ates, and animal fatty materials such as lanoline or wool-grease, and mix- 55 parts by weight of lubricating oil, preferably 5 to (3) At a temperature of 50 C. using cylinders the inside surfaces of which had been coated with oil.
  • the protective coating formed was 5 found to be uniform and firm. After standing spraying and lesser quantities such as 20 to 50 parts for other methods of application.
  • compositionzmade'inaccordance with this invention is as follows, the percentages being by weight in each case:
  • solvent a petroleum spirit or naphtha having a boiling range of from 90 to 103 C. and density of .722 at 60 F. containing about 11.5% by weight of aromatic hydrocarbonsl.
  • chlorinated-paraffin wax/naphthalene condensation product (conventional pour depressant for waxy oils). (This is a 17.5% solution in mineral oil-actual condensation product'is 0.175%
  • the sprayed cylinder sleeves were then stored together with some unsprayed sleeves in a partially open shed where they were exposed to a dusty atmosphere although being shielded from direct sunlight. After five months the sleeves were examined. The unsprayed sleeves were heavily rusted but the sprayed areas were wholly free from rust except in one case where slight spotting had occurred due to water dripping onto the sleeve from the roof of the shed.
  • composition prepared in accordance with this invention gave complete protection during accelerated corrosion tests under -conditions shown to cause extensive corrosion-of the unprotected metal.
  • O-bviouslyztheproportions of the various ingredients may be varied within the limits set forth above, and conventional modifiers, such as sodium nitrite, antioxidants such as the phenyl amines, etc., may be included if desired. Also, while 'itis suggested above that the compositions of this invention are particularly suitable for spraying into internal combustion engines, it will be obvious that they may be applied in various ways to various types of metal surfaces to protect them from rusting or other forms of oxidation-or corrosion.
  • a coating composition for protecting metal surfaces against corrosion comprising about 1 to 10 parts by weight of microcrystalline wax, 3 to 15 parts of lubricating oil, 0.01 to 0.05 part :of a polyiso-olefin, and 0.05 to 5 parts of a pour depressor for waxy'oils, said pour depressor being a condensation product of a chlorinated long chain hydrocarbon with an aromatic compound selected from the group consisting of naphthalene and phenol.
  • composition according to claim 1 to which is added a corrosion inhibitor comprising an oil soluble sulfonate.
  • a rust preventing composition for ferrous metals comprising 1 to 10 parts by weight of microcrystalline wax, 3 to l5'parts of lubricating oil, 0.01 to 0.05 part of a C3 to C14 polyiso-olefin of molecular weight between 20,000 and 200,000, 0.05 to 5 parts of a pour depressor for waxy oils, said pour depressor being a condensation product'of a chlorinated wax with an aromatic compound selected from the group consisting of naphthalene and phenol and a volatile solvent in sufficient proportions to thin the composition to convenient thickness for application to the surface to be protected.
  • a composition consisting essentially of 1 to 10 parts by weight of microcrystalline wax of melting point between and 210 F., 3 to 15 parts of mineral base lubricating oil, 0.01 to 0.05 part of .a predominantly isobutylene polymer of molecular weight between 20,000 and 200,000, 0.05 to 5 parts of the Friedel-Crafts condensation product of chlorinated wax and naphthalene, 0.5 to 2 parts of a corrosion inhibitor comprising oil soluble .metal petroleum sulfonate and lanoline, .and .20 to 100 parts of a hydrocarbon 33182620 having a boiling point between 40 and 5.
  • a composition consisting essentially of 3 to 8 parts by weight of microcrystalline wax having a melting point .between 180 and 200 F 5 to 10 parts of mineral base lubricating oil, 0.01 to 0.05 part of polyisobutylene, 0.2 to 1.0 part of the Friedel-Cra'fts condensation product of chlorinated wax and naphthalene, 0.5 to 2.0 parts of a combination of oil soluble sodium sulfonate and degras, and 50 to 100 parts of a hydrocarbon s01- chaving a boiling point between 70 and 6.
  • a composition consisting essentially of about 84% by weight of petroleum hydrocarbon boiling between 90 and 103 C., 5% microcrystalline Wax melting between 180 and 200 F., 8.5% mineral lubricating oil, 1% soluble sodium sulfon'ate, 0.5% degrasj .175% chlorinated wax 5 naphthalene condensation product pour point depressor, and 0.02% polyisobutylene of 40,000 to 100,000 molecular weight.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)

Description

Patented Aug. 11, 1953 ENGINE CORROSION PREVENTIVE William Henry Adams and William Denis Ervine, Kingston, England, assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application June 21, 1950, Serial I No. 169,516. In Great Britain August 15, 1949 6 Claims.
The present invention relates to improved corrosion preventive compositions which may be applied to metal surfaces, especially ferrous metal surfaces, to form protective coatings.
The invention is particularly concerned with the production of wax-containing compositions which have good adhesion properties when applied to metal surfaces.
It is well known that internal combustion engines, when left idle for extended periods after use, suffer corrosion particularly of the cylinder walls, piston and cylinder head. In consequence the use of corrosion inhibiting oils containing 011- soluble corrosion inhibitors has been widely practised, but difficulty has been experienced due to draining of the protective film'and it has been proposed to add waxes to the corrosion preventive composition to give the film greater mechanical strength. Such wax-thickened oils have in practice been blended with a volatile solvent or solvents to enable the composition to be sprayed into the engine cylinders.
After evaporation of the volatile solvent, the waxy film should form a protective coating over the Whole of the exposed metal surface, but it has been found that the film frequently cracks and even, in some cases, slips bodily over the surface exposing part of it to corrosion.
It has now been discovered that the structure of the wax coating may be modified by the addition to the wax of minor proportions of well known types of pour point depressor which are conventionally used with lubricating oils, together with a high molecular Weight polyiso-olefin. The effects of these wax modifiers are such that the adherence of the coating to the metal is greatly' The pour point depressor is preferably a Friedel- Crafts condensation product of the halogenated long-chain hydrocarbon and aromatic type, e. g. a chlorinated parafiin Wax and naphthalene but other known and generally equivalent pour point depressors such as chlorinated wax-phenol compounds may be used.
The polyiso-olefin to be used may be any C3 to C14 iso-olefin polymer having a molecular weight between 20,000 and 200,000 but is preferably a polyisobutylene and preferably has a molecular weight between 40,000 and 100,000. The copolymers of similar properties, such as Butyl rubber, which is a copolymer predominantly of isobutylene with small proportions of a multiolefin such as isoprene, may be used for the same purposes.
The wax-containing corrosion preventive may comprise essentially a de-oiled petrolatum wax, i. e., a microcrystalline petroleum wax, a volatile solvent in which the wax is sparingly soluble at room temperature and readily soluble when hot, a lubricating oi1 and, usually but not always necessarily, minor proportions of conventional corrosion inhibitors.
The composition may be prepared by melting the wax together with the pour point depressor, the polyiso-olefin, the lubricating oil and corrosion inhibitors, dissolving this mixture in the moderately heated volatile solvent and chilling the solution rapidly and with agitation. This allows the formation of a suspension of microcrystalline wax of very fine particle size having a good degree of stability.
The wax used should preferably be a hard deoiled petroleum wax such as a mi-crocrystalline petroleum wax having a melting point in the range to 210 F. and one having a melting point between 180 and 200 F; is preferred.
The solvent may be any volatile solvent boiling, for example, in the range 40 to C. and in which the wax is sparingly soluble at room temperature and readily soluble at higher temperatures but it is preferred that a hydrocarbon solvent be used and it is most convenient that the solvent chosen should have a boiling range between 70 and 120 C.
prove the texture of the coating and enhance cor-' rosion prevention.
Examples of conventional corrosion inhibitors are the alkali-metal and alkaline earth metal oilsoluble petroleum sulphonates, particularly sodium petroleum sulphon'ates, and animal fatty materials such as lanoline or wool-grease, and mix- 55 parts by weight of lubricating oil, preferably 5 to (3) At a temperature of 50 C. using cylinders the inside surfaces of which had been coated with oil.
In each case the protective coating formed was 5 found to be uniform and firm. After standing spraying and lesser quantities such as 20 to 50 parts for other methods of application.
An example of a compositionzmade'inaccordance with this invention is as follows, the percentages being by weight in each case:
83.8% solvent (a petroleum spirit or naphtha having a boiling range of from 90 to 103 C. and density of .722 at 60 F. containing about 11.5% by weight of aromatic hydrocarbonsl.
5.0% amber microcrystalline wax (melting point 8.5% aircraft engine oil.
'1-.0% sodium petroleum sulphonates of about 400:1:0 450 molecular weight.
0;5%' lanoline (degras).
1.0% chlorinated-paraffin wax/naphthalene condensation product (conventional pour depressant for waxy oils). (This is a 17.5% solution in mineral oil-actual condensation product'is 0.175%
0.2% :polyisobutyl-ene (M. W. 40,000-100,000) in oil solution.
In one series of tests the inside surfaces of a number of aircraft engine cylinder sleeves were sprayed. at room temperature with the above composition. Each sleeve was dry and free from oilzand the piston was fitted into the sleeve, the spraying being done through the orifices.
In order that the conditions should simulate as much as possible those encountered in workshops, some of the sleeves were sprayed with the piston at top dead-centre and some were sprayed with the piston at the bottom deadcentre and some of each were allowed to remain as they were while others had the pistons .moved from top to bottom or from bottom to top after the spraying.
'In-some cases a single charge of 5 cos. of the composition was sprayed onto the surface of each cylinder sleeve while in other cases two charges each of 5 cos. were sprayed.
The sprayed cylinder sleeves were then stored together with some unsprayed sleeves in a partially open shed where they were exposed to a dusty atmosphere although being shielded from direct sunlight. After five months the sleeves were examined. The unsprayed sleeves were heavily rusted but the sprayed areas were wholly free from rust except in one case where slight spotting had occurred due to water dripping onto the sleeve from the roof of the shed.
Where some sleeves had some areas sprayed and other areas left unsprayed, the demarcation line between the sprayed and unsprayed areas was very marked.
It was found that equal protection was given by the single spraying and by the double spraying and there was no deterioration in the sleeves where the piston had been moved after spraying.
Other tests were carried out under different conditions, that is:
(1) At room temperatures using cylinders the inside surfaces of which had been coated with oil.
(2) At a temperature of 50 C. using cylinders the inside surfaces of which were dry and free from oil.
for several months there was no sign .of cracking or crazing of the wax surface and no sign of any slippage. The composition prepared in accordance with this invention gave complete protection during accelerated corrosion tests under -conditions shown to cause extensive corrosion-of the unprotected metal.
O-bviouslyztheproportions of the various ingredients may be varied within the limits set forth above, and conventional modifiers, such as sodium nitrite, antioxidants such as the phenyl amines, etc., may be included if desired. Also, while 'itis suggested above that the compositions of this invention are particularly suitable for spraying into internal combustion engines, it will be obvious that they may be applied in various ways to various types of metal surfaces to protect them from rusting or other forms of oxidation-or corrosion.
What is claimed is:
1. A coating composition for protecting metal surfaces against corrosion, comprising about 1 to 10 parts by weight of microcrystalline wax, 3 to 15 parts of lubricating oil, 0.01 to 0.05 part :of a polyiso-olefin, and 0.05 to 5 parts of a pour depressor for waxy'oils, said pour depressor being a condensation product of a chlorinated long chain hydrocarbon with an aromatic compound selected from the group consisting of naphthalene and phenol.
2. Composition according to claim 1 to which is added a corrosion inhibitor comprising an oil soluble sulfonate.
3. A rust preventing composition for ferrous metals, comprising 1 to 10 parts by weight of microcrystalline wax, 3 to l5'parts of lubricating oil, 0.01 to 0.05 part of a C3 to C14 polyiso-olefin of molecular weight between 20,000 and 200,000, 0.05 to 5 parts of a pour depressor for waxy oils, said pour depressor being a condensation product'of a chlorinated wax with an aromatic compound selected from the group consisting of naphthalene and phenol and a volatile solvent in sufficient proportions to thin the composition to convenient thickness for application to the surface to be protected.
4. A composition consisting essentially of 1 to 10 parts by weight of microcrystalline wax of melting point between and 210 F., 3 to 15 parts of mineral base lubricating oil, 0.01 to 0.05 part of .a predominantly isobutylene polymer of molecular weight between 20,000 and 200,000, 0.05 to 5 parts of the Friedel-Crafts condensation product of chlorinated wax and naphthalene, 0.5 to 2 parts of a corrosion inhibitor comprising oil soluble .metal petroleum sulfonate and lanoline, .and .20 to 100 parts of a hydrocarbon 33182620 having a boiling point between 40 and 5. A composition consisting essentially of 3 to 8 parts by weight of microcrystalline wax having a melting point .between 180 and 200 F 5 to 10 parts of mineral base lubricating oil, 0.01 to 0.05 part of polyisobutylene, 0.2 to 1.0 part of the Friedel-Cra'fts condensation product of chlorinated wax and naphthalene, 0.5 to 2.0 parts of a combination of oil soluble sodium sulfonate and degras, and 50 to 100 parts of a hydrocarbon s01- chaving a boiling point between 70 and 6. A composition consisting essentially of about 84% by weight of petroleum hydrocarbon boiling between 90 and 103 C., 5% microcrystalline Wax melting between 180 and 200 F., 8.5% mineral lubricating oil, 1% soluble sodium sulfon'ate, 0.5% degrasj .175% chlorinated wax 5 naphthalene condensation product pour point depressor, and 0.02% polyisobutylene of 40,000 to 100,000 molecular weight.
WILLIAM HENRY ADAMS. WILLIAM DENIS ERVINE.
References Cited in the file of this patent UNITED STATES PATENTS Number Name Date MacLaren June 19, 1934 Lebo Dec. 12, 1939 Adams et a1. May 16, 1944 Wright Aug. 22, 1944 Sudholz et a1. Oct. 10, 1944 Davis et a1 Nov. 16, 1948 Morgan Aug. 28, 1951

Claims (1)

  1. 4. A COMPOSITION CONSISTING ESSENTIALLY OF 1 TO 10 PARTS BY WEIGHT OF MICROCRYSTALLINE WAX OF MELTING POINT BETWEEN 135* AND 210* F., 3 TO 15 PARTS OF MINERAL BASE LUBRICATING OIL, 0.01 TO 0.05 PART OF A PREDOMINANTLY ISOBUTYLENE POLYMER OF MOLECULAR WEIGHT BETWEEN 20,000 AND 200,000, 0.05 TO 5 PARTS OF THE FRIEDEL-CRAFTS CONDENSATION PRODUCT OF CHLORINATED WAX AND NAPHTHALENE, 0.5 TO 2 PARTS OF A CORROSION INHIBITOR COMPRISING OIL SOLUBLE METAL PETROLEUM SULFONATE AND LANOLINE, AND 20 TO 100 PARTS OF A HYDROCARBON SOLVENT HAVING A BOILING POINT BETWEEN 40* AND 190* C.
US169516A 1949-08-15 1950-06-21 Engine corrosion preventive Expired - Lifetime US2648643A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB21156/49A GB667042A (en) 1949-08-15 1949-08-15 Improved engine corrosion preventive

Publications (1)

Publication Number Publication Date
US2648643A true US2648643A (en) 1953-08-11

Family

ID=10158121

Family Applications (1)

Application Number Title Priority Date Filing Date
US169516A Expired - Lifetime US2648643A (en) 1949-08-15 1950-06-21 Engine corrosion preventive

Country Status (2)

Country Link
US (1) US2648643A (en)
GB (1) GB667042A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2746910A (en) * 1953-03-10 1956-05-22 Sun Oil Co Adhesive wax composition
US2766157A (en) * 1953-01-15 1956-10-09 Preformed Line Products Co Method of protecting and connecting mating electrical conductor members
US2843548A (en) * 1954-10-01 1958-07-15 Exxon Research Engineering Co Rust preventive aviation oil
US3004917A (en) * 1959-05-14 1961-10-17 Exxon Research Engineering Co Oil compositions containing rust inhibitors
US3080330A (en) * 1959-05-29 1963-03-05 Exxon Research Engineering Co Rust preventive compositions of paraffinic mineral oil thickened with polyethylene and microcrystalline wax
US3258319A (en) * 1962-11-23 1966-06-28 Du Pont Lubricant coated formable metal article
US4675215A (en) * 1985-09-27 1987-06-23 Economics Laboratory, Inc. Method and composition for the inhibition of corrosion
US4749412A (en) * 1985-09-27 1988-06-07 Drew Chemical Corporation Method and composition for the inhibition of corrosion

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3455716A (en) * 1962-10-08 1969-07-15 Sinclair Research Inc Coating composition
US20170267869A1 (en) 2014-08-22 2017-09-21 Frans Nooren Afdichtingssystemen B.V. Composition for the protection of an article against corrosion
CN116376439A (en) * 2023-04-07 2023-07-04 沈阳帕卡濑精有限总公司 Protective wax for industrial electronic circuit board and preparation method and application thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1963917A (en) * 1933-01-18 1934-06-19 Standard Oil Co Pour test depressor
US2182992A (en) * 1937-09-24 1939-12-12 Stanco Inc Corrosion preventive
US2348715A (en) * 1941-06-25 1944-05-16 Standard Oil Co Slushing composition
US2356367A (en) * 1940-11-22 1944-08-22 Jasco Inc High temperature lubricant
US2359946A (en) * 1941-06-11 1944-10-10 Socony Vacuum Oil Co Inc Slushing compositions
US2453833A (en) * 1944-08-05 1948-11-16 Standard Oil Dev Co Corrosion preventive
US2566068A (en) * 1948-01-06 1951-08-28 Cities Service Res & Dev Co Corrosion inhibiting compounds

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1963917A (en) * 1933-01-18 1934-06-19 Standard Oil Co Pour test depressor
US2182992A (en) * 1937-09-24 1939-12-12 Stanco Inc Corrosion preventive
US2356367A (en) * 1940-11-22 1944-08-22 Jasco Inc High temperature lubricant
US2359946A (en) * 1941-06-11 1944-10-10 Socony Vacuum Oil Co Inc Slushing compositions
US2348715A (en) * 1941-06-25 1944-05-16 Standard Oil Co Slushing composition
US2453833A (en) * 1944-08-05 1948-11-16 Standard Oil Dev Co Corrosion preventive
US2566068A (en) * 1948-01-06 1951-08-28 Cities Service Res & Dev Co Corrosion inhibiting compounds

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2766157A (en) * 1953-01-15 1956-10-09 Preformed Line Products Co Method of protecting and connecting mating electrical conductor members
US2746910A (en) * 1953-03-10 1956-05-22 Sun Oil Co Adhesive wax composition
US2843548A (en) * 1954-10-01 1958-07-15 Exxon Research Engineering Co Rust preventive aviation oil
US3004917A (en) * 1959-05-14 1961-10-17 Exxon Research Engineering Co Oil compositions containing rust inhibitors
US3080330A (en) * 1959-05-29 1963-03-05 Exxon Research Engineering Co Rust preventive compositions of paraffinic mineral oil thickened with polyethylene and microcrystalline wax
US3258319A (en) * 1962-11-23 1966-06-28 Du Pont Lubricant coated formable metal article
US4675215A (en) * 1985-09-27 1987-06-23 Economics Laboratory, Inc. Method and composition for the inhibition of corrosion
US4749412A (en) * 1985-09-27 1988-06-07 Drew Chemical Corporation Method and composition for the inhibition of corrosion

Also Published As

Publication number Publication date
GB667042A (en) 1952-02-20

Similar Documents

Publication Publication Date Title
US2631979A (en) Rust inhibiting composition
US2648643A (en) Engine corrosion preventive
US2564423A (en) Corrosion preventive composition
US2497521A (en) Oil compositions containing amine salts of boro-diol complexes
US2348715A (en) Slushing composition
US2956020A (en) Anti-corrosion compositions
US2862800A (en) Gasoline fuels
US2417876A (en) Inhibited oil
US2564422A (en) Corrosion preventive composition
US2833717A (en) Corrosion inhibiting lubricating oil
US3169116A (en) Corrosion inhibiting compsoitions
US2383033A (en) Lubricants
US2602049A (en) Antioxidants for mineral oil lubricants and compositions containing the same
US2484010A (en) Corrosion inhibitor
US2378442A (en) Mineral oil composition
US3086871A (en) Coating composition
US2362332A (en) Corrosion preventive compositions
US2533300A (en) Morpholine mahogany sulfonate as a rust inhibitor for petroleum oils
US2843548A (en) Rust preventive aviation oil
US2442581A (en) Rust-preventive composition
US2471638A (en) Rust preventive compositions
US2450321A (en) Rust-inhibiting greases
US2480754A (en) Chromium-containing phenolic amine reaction product
US3086870A (en) Coating composition and method
US2283931A (en) Rust preventive compound