US2235944A - Rust prevention and removal - Google Patents

Rust prevention and removal Download PDF

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US2235944A
US2235944A US96522A US9652236A US2235944A US 2235944 A US2235944 A US 2235944A US 96522 A US96522 A US 96522A US 9652236 A US9652236 A US 9652236A US 2235944 A US2235944 A US 2235944A
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Nicholas G Penniman
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/08Anti-corrosive paints
    • 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
    • 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
    • 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
    • C10M2201/086Chromium oxides, acids or salts
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02Hydroxy compounds
    • C10M2207/021Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
    • 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
    • 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
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/08Aldehydes; Ketones
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/16Naphthenic acids
    • 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
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/20Rosin acids
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/02Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • 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
    • C10M2209/00Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/101Condensation polymers of aldehydes or ketones and phenols, e.g. Also polyoxyalkylene ether derivatives thereof
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/02Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only
    • C10M2211/022Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen and halogen only aliphatic
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/04Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
    • C10M2211/042Alcohols; Ethers; Aldehydes; Ketones
    • 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
    • C10M2211/00Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
    • C10M2211/06Perfluorinated compounds
    • 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
    • C10M2223/00Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
    • C10M2223/02Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
    • C10M2223/04Phosphate esters
    • C10M2223/041Triaryl phosphates
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/08Groups 4 or 14
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/14Group 7
    • 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
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/16Groups 8, 9, or 10
    • 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

Definitions

  • This invention relates to 'composltions for preventing the oxidation of metals, particularly iron, and for the removal of rust or similar oxidized material from such metal surfaces, as well as 5 compositions possessing both'of the attributes referred-to, and also to methods of producing and utilizing such compositions, and to articles carry 'lng' surface protecting coatings produced with such compositions.
  • i 1 While a number of' compositions have been suggested in the prior art for use as rust preventing materials, these compositions have not generally proved satisfactory inpractice.
  • the various types of proposed prior art compositions have failed to produce protective coatings sufficient to prevent the oxidation or rusting of metal surfaces on which they were applied, such failures being particularly noticeable after long periods ofexposure.
  • rust or other oxidized materials surfaces against the formation of rust or other oxidized materials, and also desirably enable ready removalof any oxidized materials or rust that may form on such metal surfaces, even ture which isto be or has been exposed to the atmosphere or other corrosive media.
  • Other objects of the present invention include the methods of utilizing such compositions in 55 the protection of the indicatedmetal surfaces,
  • compositions which protect after or during storage over long periods of time:
  • compositions are desirably employed which pro tect metal surfaces against rusting or undesired oxidative change, or enable ready removal of any oxidized or rusted spots on such metal.
  • mineral these'mineral and petroleum oils and theirfractions and distillates, however, do not exhibit properties in and of themselves sufficient for the indicated purposes, and accordingly components are included therewith, preferably soluble in the petroleum or mineral oil fraction or distillate,
  • a particularly important typeof component to be utilized, in such compositions includes materials which increase the lnterfacial tension of such compositions with respect to metal surfaces.
  • Polar bodies generally exhibit such properties, and among such polar bodies there may particularly be mentioned the higher'fatty acids, particularly of unsaturated character, such as oleic acids.
  • the higher'fatty acids particularly of unsaturated character, such as oleic acids.
  • polar bodies that may be utilized are exemplified'by aw'ide variety of materials among which the following may be noted: ketones, aldehydes, alcohols orinixed derivatives of the allphatic, unsaturated, or benzeneseries, as well as In some instances it is found 3 the naphthenes.
  • ketones aldehydes, alcohols orinixed derivatives of the allphatic, unsaturated, or benzeneseries, as well as In some instances it is found 3 the naphthenes.
  • various compounds of the hydrocarhon type contahiingWsulphur bound in the molecule, or 'thexderivatives of such product are exemplified'by aw'ide variety of materials among which the following may be noted: ketones, aldehydes, alcohols orinixed derivatives of the allphatic, unsaturated, or benzeneseries, as well as In some instances it is found 3 the naphthenes.
  • Sillpllllili-IIOE only increases .the penetrative' properties at the composition, but also adds to the protective qualities of the coating by combinin chemically with any rust that may be present, and thus forming protective layers. Both the protective and penetrative efiects of the sulphur compound are sometimes assisted by incorporating into the same compound or composition some of the halogens, and in some instances oxygen,
  • hydrocarbon derivatives which contain the sulphur and the halogen or the sulphur and the oxygen, or all three of such components, bound into the molecule.
  • compositions for the purposes herein set forth.
  • various drying oils either separately or in combination, including both the vegetable and animal oils, may be employed.
  • oils should be given a special treatment, difierent in many cases from that of an ordinary paint oil, though the usual operations of blowing, boiling, etc. are naturally and desirably included. It.has been found that perilla and linseed oils are more generally useful than other oils, but for many special purposes wood oil, soya bean oil and flsh oil may be used either separately or in combination.
  • the protective action of the drying oil may be accelerated by the inclusion of driers in the composition.
  • driers including the common lead, cobalt and manganese driers may pared oils on the market alre but it has been found in general that by the use be employed for this purpose. Many of the precontain driers of special driers the protective properties of the resulting compound can be noticeably increased. It has also been found desirable at times in choosing the driers. to exercise care that the agent included for the purpose of accelerating oil-oxidation shall not also be capable of promating the oxidation'and corrosion of the iron or other metal surface.
  • the film materials need not, however, be limited to the siccatiye oils, but other types of materials, such as the resins, both natural and synthetic may be employed.
  • the resins both natural and synthetic may be employed.
  • nat-- ural resins there may be mentioned cumar, damar, kauri, manila, pontianak, sandarac, and rosin, as well as the esters of the acid resins'such as rosin ester. etc.
  • resins may be chosen from the synthetic resins, including, for example, resins of the phenolformaldehyde type. of the phthalic-glyceride type, etc. Such resins. Particularly of the oilsoluble type, that is, soluble in mineral. oils or fractions or distillates thereof are the most desirable types to be employed.
  • waxes either of the mineral or vegetable types
  • the former include paraflln, ceresin, and ozokerite.
  • rancid oils may be employed as a source I of .the polar bodies, such rancid oils containing oleic and other acids. And when such rancid oils assasss are employed, they offer a source of both the film-forming or sponge-forming materials, as well as the polar bodies.
  • the various glyceride oils employed may be given a partial hydrolysis or .saponification if desired, to produce acids therein for such purposes.
  • compositions are desirably chosen that will produce solutions, since clear solutions of the components or compositions which are apparently in homogeneous condition are more desirably employed.
  • emulsions, suspensions, and dispersions of various types may be employed for satisfactory use in this connection.
  • pine oil 2% pine oil 2%, oleic acid 2%, drier 0.5%, and the balance petroleum oil. 4
  • composition illustrating a spe- .ciflc formulation is the following: bodied perilla oil, 5%; oleic acid, 1%; drler,.1%.; pine oil, 2%;
  • the proportions indicated are not limiting since various proportions of the stated ingredients can be utilized.
  • the bulk of the composition should desirably be a' mineral oil fraction or petroleum oil fraction, or distillate, and desirably will constitute the major proportion of the composition
  • a lesser proportion of the film-forming materia such as the siccative oil, may be employed, whereas the other components need be present only in. minor proporrtions.
  • the polar body should be present in a sufflcien-t amount to give the composition the desired interfacial tension.
  • Trlcresylphosphate or other chemical inhibitor may be used in proportions of from -1 to 10%.
  • anyof the sulphurized oils may be employed, the particular product used depending to some degree on the material available to the. manufacturer, at least cost.
  • Various ways of producing sulphurized oils, minerals, vegetable or animal may be employed and the following is merely illustrative of one such procedure.
  • a desired quantity of lard oil is heated to about 400 F. (200 C.) and small quantities of sulphur added to the heated -oil from time to time until the total amount of sulphur used is equal to about 26% based on the lard oil.
  • Considerable sulphur is lost by volatilization as sulphur derivatives; but the heating is continueduntil the-sulphur which remains in the composition is in'such com-,
  • the resulting product is such that the sulphur present in combined state still exists in a condition where it has an attraction for the metal surface so that the sulphur compounds attach themselves to the a J Y terial.
  • the compositions of the character set forthherein particularly when containu metallic surface to act as a polar body and to form a protective component of the composition.
  • the siccative oil is given a preliminary oxidation to an extent suificientto enable that oxidation to continuein the presence of the drier, in connection with compositions employed in accordance with the present invention, the oxidative change in the siccative is desirably carried further so that it' will also enhance oreffect a change in the petroleum oil or distillate.
  • driers may be. utilized in the presentcompositions to the extent of 4 or 5 times as much as those employedin ordinary paint and varnish compositions.
  • compositions illustrated by the examples given above exhibit not alone desirable properties of protecting the surfaces against rust, but
  • compositions also exhibit'many other desirable properties. Any rust or oxidized spots that may appear on the metal surfaces are readily removed example, remain-in contact with water.
  • the surface which has carried a protective composition of the-character set forth herein is in a much better condition for the reception of paint than such a surface would be had it carried merely a petroleum ma ing the polar bodies, such as oleic acid, are of exceptionally desirable character, since these com-:- positions penetrate into any minor cracks or irregularities at the surface of. the metal, and a give protection which is carried into those 'defective portions of the metal.
  • the penetration power of the composition may be increased by including therein a more or less volatile solvent particularly of organic character.
  • the degree of penetration is 'effected by the viscosity of the composition as well as the interfacial tension. While the petroleum derived ingredients are inexpensive and reduce the viscosity, the interfacial tension of these materials is not marked.
  • chlorinated compounds ranging from car-.- bontetrachloride on the one handto the more complex chlorinated derivatives, such as trichlor-. ethylene, etc. may be utilized since they act to produce the requisite reduction in viscosity and also at the same time toincrease the interfacial tension of such compositions containing such in+ gradients.
  • a wide "variety of the liquid chlorinated hydrocarbon of the aliphatic series may thus be employed'but desirably such-components are utilized. in the compositions when the latterare applied to surfaces not confined in-enclosed' spaces.
  • the amounts of the chlorinated derivatives employed may vary within rather wide? limits but in general need not exceed about 10% of the mixture, although in sbme instances larger amounts can be employed advantageously for special uses.
  • Other volatile materials particularly aliphatic hydrocarbon derivatives including 'ethers, ketones, aldehydes, etc..rnay be employed or mixtures of chlorinated and non-chlorinated volatile substances can be utilized.
  • v 1 A rust preventing and removing. composition comprising about 10% of boiled linseed oil; in: cluding drier,'2% of pine oil, 2% of oleic acid an the remainder petroleum oil distillate. J a
  • a rust preventing and removing composition which forms a tacky coating, said compositioncomprising from 5 to 20% of boiled linseed oil, 0.1 to 5% drier, 1 to 5% pine oil, 0.5 to 5% of oleic acid, and the remainder petroleum oil distillate .50 WILLIAM B. p. PENNIMAN.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

. Patented Mar. 25, 1 941 amass aus'r maven-non Am), Remover.
William B. n. Penniman, Baltimore, mi; Nicholas G. Penniman, III, executor oi said William n.
Penniman, deco No Drawing. Application Riugusi i'l, was,
i Serial No. 98,522
This invention relates to 'composltions for preventing the oxidation of metals, particularly iron, and for the removal of rust or similar oxidized material from such metal surfaces, as well as 5 compositions possessing both'of the attributes referred-to, and also to methods of producing and utilizing such compositions, and to articles carry 'lng' surface protecting coatings produced with such compositions. i 1 While a number of' compositions have been suggested in the prior art for use as rust preventing materials, these compositions have not generally proved satisfactory inpractice. The various types of proposed prior art compositions have failed to produce protective coatings sufficient to prevent the oxidation or rusting of metal surfaces on which they were applied, such failures being particularly noticeable after long periods ofexposure. For example, in connectionwith metal 0 ships and boats, protection of the metal surfaces against oxidative changes and rusting is particularly necessary as when such vessels may be tied up for storage and other purposes, and particularly-when such non-use extends over relatively long periods of time. Furthermore, when such ships or boats are, returned to service, repainting of the metal surfaces is generally required, and unless the composition has properties of enabling ready removal of any oxidized matter or rust, etc. from the surfaces, elaborate cleaning methods are required before adequate paint coatings can be applied. It is also "essential that any residual jfilmof material left on the surface after the removal of the protective, coating must be such as not to affect adversely the adherence. or
other properties of the paint which is to be applied.. Prior art compositions have not proved satisfactory for any of these purposes.
Among the objects of the present invention is surfaces against the formation of rust or other oxidized materials, and also desirably enable ready removalof any oxidized materials or rust that may form on such metal surfaces, even ture which isto be or has been exposed to the atmosphere or other corrosive media. Other objects of the present invention include the methods of utilizing such compositions in 55 the protection of the indicatedmetal surfaces,
the production of compositions which protect after or during storage over long periods of time:
(Cl. lM-U and also the articles themselves when carrying such protective coating.
Still further objects and advantages will appear from the more detailed description set forth xbelow, it being understood, however, that this more detailed description is given by way of iilustration and explanation only, and not by way of limitation, since various changes therein may be made by those skilled, in the art without departing from the scope and spirit of the present invention. I,
In accordance with the present invention, compositions are desirably employed which pro tect metal surfaces against rusting or undesired oxidative change, or enable ready removal of any oxidized or rusted spots on such metal. As the main body or vehicle of such composition, mineral These'mineral and petroleum oils and theirfractions and distillates, however, do not exhibit properties in and of themselves sufficient for the indicated purposes, and accordingly components are included therewith, preferably soluble in the petroleum or mineral oil fraction or distillate,
which give such compositions valuable properties for use for these purposes. A particularly important typeof component to be utilized, in such compositions includes materials which increase the lnterfacial tension of such compositions with respect to metal surfaces.. Polar bodies generally exhibit such properties, and amongsuch polar bodies there may particularly be mentioned the higher'fatty acids, particularly of unsaturated character, such as oleic acids. However, the
' types of polar bodies that may be utilized are exemplified'by aw'ide variety of materials among which the following may be noted: ketones, aldehydes, alcohols orinixed derivatives of the allphatic, unsaturated, or benzeneseries, as well as In some instances it is found 3 the naphthenes. desirable to employ as the-polar sulfostance, or substances, various compounds of the hydrocarhon type contahiingWsulphur bound in the molecule, or 'thexderivatives of such product.
illlhen suitably blended with the organic mate rial, Sillpllllili-IIOE only increases .the penetrative' properties at the composition, but also adds to the protective qualities of the coating by combinin chemically with any rust that may be present, and thus forming protective layers. Both the protective and penetrative efiects of the sulphur compound are sometimes assisted by incorporating into the same compound or composition some of the halogens, and in some instances oxygen,
thus producing hydrocarbon derivatives which contain the sulphur and the halogen or the sulphur and the oxygen, or all three of such components, bound into the molecule.
In addition to the layer of coating immediately in contact with the metal, which is formed by the polar bodies, it is also desirable to build up other layers above the initial or polar layer. In particular it is important to includein the composition, components which will produce a layer or membrane at the surface of contact between the coating and the air, as such surface layers add considerably to the abrasionand weatherresistant properties of the coating, Desirably, however, formation of a hard final coating which would be difllcult of removal, is avoided in compositions for the purposes herein set forth. For producing the additional layer just referred to, the various drying oils either separately or in combination, including both the vegetable and animal oils, may be employed. In general such oils should be given a special treatment, difierent in many cases from that of an ordinary paint oil, though the usual operations of blowing, boiling, etc. are naturally and desirably included. It.has been found that perilla and linseed oils are more generally useful than other oils, but for many special purposes wood oil, soya bean oil and flsh oil may be used either separately or in combination.
The protective action of the drying oil may be accelerated by the inclusion of driers in the composition. Various types of driers including the common lead, cobalt and manganese driers may pared oils on the market alre but it has been found in general that by the use be employed for this purpose. Many of the precontain driers of special driers the protective properties of the resulting compound can be noticeably increased. It has also been found desirable at times in choosing the driers. to exercise care that the agent included for the purpose of accelerating oil-oxidation shall not also be capable of promating the oxidation'and corrosion of the iron or other metal surface.
The film materials need not, however, be limited to the siccatiye oils, but other types of materials, such as the resins, both natural and synthetic may be employed. As exemplary of nat-- ural resins there may be mentioned cumar, damar, kauri, manila, pontianak, sandarac, and rosin, as well as the esters of the acid resins'such as rosin ester. etc.
However, where resins are employed they de-- sirably may be chosen from the synthetic resins, including, for example, resins of the phenolformaldehyde type. of the phthalic-glyceride type, etc. Such resins. Particularly of the oilsoluble type, that is, soluble in mineral. oils or fractions or distillates thereof are the most desirable types to be employed.
. In addition to resins it has been found very useful at times to .use one or more waxes either of the mineral or vegetable types, The former include paraflln, ceresin, and ozokerite. Among the more useful vegetable waxes there may be particularlymentioned Japan wax, candellila, carnauba, beeswax, bayberry wax, etc.
Where glyceride oils are employed in the composition, rancid oils may be employed as a source I of .the polar bodies, such rancid oils containing oleic and other acids. And when such rancid oils assasss are employed, they offer a source of both the film-forming or sponge-forming materials, as well as the polar bodies. The various glyceride oils employed may be given a partial hydrolysis or .saponification if desired, to produce acids therein for such purposes.
Other components may be included for their special function, such as pine oil, and rosin 011.
Other special ingredients are those used as chemical inhibitors of corrosion such as ammonium chromate or tricresylphosphate.
In compounding the compositions, materials are desirably chosen that will produce solutions, since clear solutions of the components or compositions which are apparently in homogeneous condition are more desirably employed. However, emulsions, suspensions, and dispersions of various types may be employed for satisfactory use in this connection.
A specific example of a particular type of material that may be and has been desirably employed in this connection is illustrated by the following: 10% boiled linseed oil, including drier,
pine oil 2%, oleic acid 2%, drier 0.5%, and the balance petroleum oil. 4
' Another type of composition illustrating a spe- .ciflc formulation is the following: bodied perilla oil, 5%; oleic acid, 1%; drler,.1%.; pine oil, 2%;
tricresylphosphate, 5%; and the remainder, pe- I troleum oil.
The proportions indicated are not limiting since various proportions of the stated ingredients can be utilized. However, the bulk of the composition should desirably be a' mineral oil fraction or petroleum oil fraction, or distillate, and desirably will constitute the major proportion of the composition A lesser proportion of the film-forming materia such as the siccative oil, may be employed, whereas the other components need be present only in. minor proporrtions. The polar body should be present in a sufflcien-t amount to give the composition the desired interfacial tension.
For particular purposes the following will illustrate variations in the proportions of ingredients that may be employed: 5 to 20% of the siccative oil, 1 to 5% of pine oil, 0.5 to 5% of the polar material, suchas oleic acid, and 0.1 to 5% of drier. Trlcresylphosphate or other chemical inhibitor may be used in proportions of from -1 to 10%.
Sulphur compounds or sulphurized products have been indicated above as particularly desirable for use as polar bodies as exemplary thereof anyof the sulphurized oils may be employed, the particular product used depending to some degree on the material available to the. manufacturer, at least cost. Various ways of producing sulphurized oils, minerals, vegetable or animal may be employed and the following is merely illustrative of one such procedure. A desired quantity of lard oil is heated to about 400 F. (200 C.) and small quantities of sulphur added to the heated -oil from time to time until the total amount of sulphur used is equal to about 26% based on the lard oil. Considerable sulphur is lost by volatilization as sulphur derivatives; but the heating is continueduntil the-sulphur which remains in the composition is in'such com-,
bination that a bright copper strip immersed for five minutes in the heated mixture or compound is not more than slightly tarnished, the resulting product is such that the sulphur present in combined state still exists in a condition where it has an attraction for the metal surface so that the sulphur compounds attach themselves to the a J Y terial. lnaddition, the compositions of the character set forthherein, particularly when containu metallic surface to act as a polar body and to form a protective component of the composition.
It has been pointed out above that the vegetable oils or other siccative oils employed in the composition in amounts less than the hydrocarbon oil or distillate maybe given special treatments to particularly adapt them to the purposes in hand, thus an oxidized siccative oil may be .car-
ried to a point of oxidation greater than that which wouldnormally, be employed for an oxidized oil'used in a coating composition of the varnish type. The reason for thisis that such treated oils not only form in time a protective or semi-protective coating or part thereof, but they also act as catalysts in inducing certain changes in the petroleum oil or fraction present in the composition. In, other words while for oidinary coating compositions like paints and v rnishes the siccative oil is given a preliminary oxidation to an extent suificientto enable that oxidation to continuein the presence of the drier, in connection with compositions employed in accordance with the present invention, the oxidative change in the siccative is desirably carried further so that it' will also enhance oreffect a change in the petroleum oil or distillate.
These considerations are further exemplified by the fact that driers may be. utilized in the presentcompositions to the extent of 4 or 5 times as much as those employedin ordinary paint and varnish compositions.
The compositions illustrated by the examples given above exhibit not alone desirable properties of protecting the surfaces against rust, but
they maintain those properties over long periods of time; since the presence of film-forming or sponge-producing layers give coatings which tend to retain themselves on the indicated surfaces.
even when boat surfaces coated therewith, for
These compositions also exhibit'many other desirable properties. Any rust or oxidized spots that may appear on the metal surfaces are readily removed example, remain-in contact with water.
'at the time that these compositions are tobe removed from the metal surfaces in preparation for a,painting operation. And in this connection,
it should be pointed out that the surface which has carried a protective composition of the-character set forth herein, is in a much better condition for the reception of paint than such a surface would be had it carried merely a petroleum ma ing the polar bodies, such as oleic acid, are of exceptionally desirable character, since these com-:- positions penetrate into any minor cracks or irregularities at the surface of. the metal, and a give protection which is carried into those 'defective portions of the metal.
If desired, the penetration power of the composition may be increased by including therein a more or less volatile solvent particularly of organic character. The degree of penetration is 'effected by the viscosity of the composition as well as the interfacial tension. While the petroleum derived ingredients are inexpensive and reduce the viscosity, the interfacial tension of these materials is not marked. On the otherhand chlorinated compounds ranging from car-.- bontetrachloride on the one handto the more complex chlorinated derivatives, such as trichlor-. ethylene, etc. may be utilized since they act to produce the requisite reduction in viscosity and also at the same time toincrease the interfacial tension of such compositions containing such in+ gradients. A wide "variety of the liquid chlorinated hydrocarbon of the aliphatic series may thus be employed'but desirably such-components are utilized. in the compositions when the latterare applied to surfaces not confined in-enclosed' spaces. The amounts of the chlorinated derivatives employed may vary within rather wide? limits but in general need not exceed about 10% of the mixture, although in sbme instances larger amounts can be employed advantageously for special uses. Other volatile materials particularly aliphatic hydrocarbon derivatives including 'ethers, ketones, aldehydes, etc..rnay be employed or mixtures of chlorinated and non-chlorinated volatile substances can be utilized.
Having thus set forth my invention, 1 claim: v 1. A rust preventing and removing. composition comprising about 10% of boiled linseed oil; in: cluding drier,'2% of pine oil, 2% of oleic acid an the remainder petroleum oil distillate. J a
2. A rust preventing and removing composition which forms a tacky coating, said compositioncomprising from 5 to 20% of boiled linseed oil, 0.1 to 5% drier, 1 to 5% pine oil, 0.5 to 5% of oleic acid, and the remainder petroleum oil distillate .50 WILLIAM B. p. PENNIMAN.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2471638A (en) * 1945-07-14 1949-05-31 Gulf Research Development Co Rust preventive compositions
US2545137A (en) * 1946-03-20 1951-03-13 Shell Dev Corrosion inhibitors
US2611711A (en) * 1948-06-18 1952-09-23 Bernard L Costello Oleaginous corrosion preventive composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2471638A (en) * 1945-07-14 1949-05-31 Gulf Research Development Co Rust preventive compositions
US2545137A (en) * 1946-03-20 1951-03-13 Shell Dev Corrosion inhibitors
US2611711A (en) * 1948-06-18 1952-09-23 Bernard L Costello Oleaginous corrosion preventive composition

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