US2318606A - Corrosion inhibition - Google Patents
Corrosion inhibition Download PDFInfo
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- US2318606A US2318606A US404832A US40483241A US2318606A US 2318606 A US2318606 A US 2318606A US 404832 A US404832 A US 404832A US 40483241 A US40483241 A US 40483241A US 2318606 A US2318606 A US 2318606A
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- metal
- long chain
- phosphates
- phosphate
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/167—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/07—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing phosphates
- C23C22/08—Orthophosphates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
Definitions
- This invention relates to corrosion inhibitors for metals and particularly to corrosion inhibitors which inhibit rust formation in ferrous metals occurring as the result of exposure to the effeet of moisture and oxygen.
- tion containing a phosphoric acid salt of a long chain aliphatic amine having at least one long chain aliphatic group of at least 8 carbon atoms attached directly to the amino nitrogen.
- a phosphoric acid salt of a long chain aliphatic amine having at least one long chain aliphatic group of at least 8 carbon atoms attached directly to the amino nitrogen.
- Another object is to provide a new and improved process for the treatment of ferrous metal surfaces so as to prevent the rusting of same. Another object is to provide new articles of commerce. A still further object is to develop corrosion inhibitors for ferrous metals which can be applied from simple aqueous systems. Another object is the treatment of ferrous metal surfaces to prevent their corrosion and further to prepare same for subsequent painting. Another object is to provide an improved process for painting. A further object'is to provide metals and particularly ferrous/metals, the surfaces of which will have a lesser tendency to be corroded and rusted. and which atthe same time will have a high receptivity for lithographic inks, paints, lacquers ,and the like.
- Another object is to provide certain new and useful compositions of matter and new articles of manufacture.
- Other objects will be apparent from the following description of the. invention- 1 These objects are accomplished by coating the surfaces of metals and particularly the surfaces offerrousmetalswlthathinfilmofacomposiphoric acid or a mono or dihydrogen phosphate, and a primary, secondary or tertiary amine having at least one long chain group of at least 8 carbon atoms attached directly to the aminonitrogen.
- the amine phosphates-. may also be obtained by reacting in the presence of water the salt of an aliphatic amine having at least one long chain group attached directly to the-amino nitrogen with a water soluble metallic salt of orthophosphoric acid.
- the phosphates formed may be either acid or neutral salts.
- phosphates when separated have been found to be exceptionally useful compounds. When applied to metal surfaces and particularly ferrous metal surfaces they have been found to have a marked rust-proofing effect. Furthermore, the surface becomes more receptive to paint film and paint films applied directly thereon adhere very well to the metal.
- the prosphates form colloidal solutions in water at elevated temperatures and may be used-in this form for treating the metal surfaces.
- Example I Two hundred parts of the mixture of alkyl amines obtainable by catalytically hydrogenating the nitriles derived from coconut oil fatty acids are added with stirring over a period of to minutes to 375 parts of 28.4% aqueous solution of HaPO4. The temperature is maintained at between and 0. during-the addition of the amine to the phosphoric acid solution. The reaction goes to completion in a short time, after which the mixture is chilled and filtered with pressure. The acid salt obtained in this way is washed with cold water and dried in an oven at 'ouite soft (grease-like) a 100! c. It
- Example II mm? v I deceny'l, hexadecenyl and octadecenylamine are also suitable.- Technicalmixtures are sometimes -.-used, as for example amines which" correspond Two hundred parts of n dodecylamine m added with stirring to 312 parts Ma 17% aqueous solution of H3904. The reaction goes to completion in a short time after which the phosphate is separated by filtration and is then dried.
- Example HI Twenty-gauge steel sheet, free from rust and grease, was dipped in a hot. 1:1 ethyl alcoholwater solution containing 4% hexadecylammonium dihydrogen phosphate and then chewed to dry in the open air. Steel panels so treated were exposed outdoors along with similar steel panels similarly treated with other commonly used protective materials. are collected in the following table:
- Example IV Steel sheet which was first phosphatized by the usual process known as Bonderiting, whereby a definite layer of iron phosphate is produced on the surface, and then sprayed with 4% octadecylamine in toluene solution was exposed out-ofdoors for three months. At the end of this period this treated 'steel was entirely rust-free, while steel sheet which had been similarly phosphatized but treated with light mineral oil was rusted heavily. Sheet which received no treatment subsequent to phosphatlzing was covered with rust over its entire surface.
- Example V A brass sheet which had been freed of dirt and grease was treated by dipping the sheet in a 4% aqueous solution of dodecyl ammonium dihydrogen phosphate maintained at 90 C. The sheet after treatment had a pleasing satin finish. The treated sheet and similar untreated sheets were exposed to an industrial atmosphere indoors for a month. At the end of this period, the untreated sheets were badly tarnished while the treated sheets possessed their original pleasing appearance.
- the amines which are useful in making the products of this invention may be classed as the long-chain aliphatic amines having said aliphatic group attached directly to the amino nitrogen atom, particularly those amines having at least tetradecyl, hexadecyl and octadecyl respectively to the alkylalcohols obtained by the catalytic hydrogenation of coconut oil acids and sperm oil; Monoamines having atleast one long chainvof less than twenty-five c'arbonatoms attached directly to the amino nitrogen atom are preferred because of availability and cost considerations, and monoamines containing at least one chain of from eight to eighteen carbon atoms attached directly to the amino nitrogen atom are particularly well suited to most of the applications where these products find use.
- Phosphoric acid salts of alkylamines having a hydrocarbon chain of from 8 to 18 carbon atoms attached directly to the amino nitrogen have been found to be particularly useful in the following The results of this exposure instances: (1) The treatment of steel subjected to high humidity and the corrosive action of perspiration, for example, during the'handling of steel during fabrication, inspection, and packing; (2) the treatment of steel requiring temporary protection during exposure to weathering: (3) the treatment of plated iron or steel articles which may be subject to corrosion due to plating defects.
- Monoalkylammonium dihydrogen phosphates Monoalkylammonlum monohydrogen phosphates Y 12 methoxyoctadecylammonium that can be used, and amines containing an unsaturated chain such as octenyl, decenyl, do-
- Di-octadecylammonium monohydrogen phosphate Tri-octadecylammonium phosphate IZ-chIgo-octadecylammonium dihydrogen phospha 12 hydroxy octadecylammonium dihydrogen f phosphate Y dihydrogen phosphate 9,10-octadecenylammohi'um dihydrogen phosphate
- Ethyldecylammonium dihydrogen phosphate Di(dimethyldodecylammonium) phosphate Trl(ethylmethyloctylammonium) phosphate monohydrogen
- R, R", and R' are hydrocarbon R, R", and R'". are hydr gen or aliphatic radicals of 8 to 24 carbon atoms connected directly to the amino nitrogen through single bonded carbon and preferably are hydrocarbon.
- Example IV illustrates the formation of the substituted ammonium phosphate on the surface metal by first forming a surface layer of metal phosphate and then applying the amine. Acidic gases of the atmosphere may take part in this reaction.
- the long-chain alkylammonlum dihydrogen phosphates are particularly useful as anticorrodents for ferrous metal surfaces. They are useful in protecting such surfaces as steel sheet, wire, tubing, and various manufactured articles.
- monohydrogen phosphates can likewise be used for these purposes, and as acid-accepting constituents of coating composition films.
- the preferred concentration lies between 2 and 10%, respectively; however, solutions containing as low as 1% or up 'to of these compounds may sometimes be used.
- the lower alcohols such as ethanol and methanol may be used as solvents, but water heated to 60 C. or more is equally suitable in most cases.
- the choice of solvent must be made, however, with regard to physical properties of the particular alkylammonium phosphate which is to be used, since in general these compounds become more soluble in organic solvents and less soluble in water as the hydrocarbon content of the molecule increases.
- a material which melts at reasonably low temperatures and which undergoes no decomposition in the region of its melting point may be applied in the liquid form without a diluent of any kind, provided that the application of the material is so regulated that the final protective film conforms to the desired thickness limits.
- These compounds may also be applied to the metal surface as a finely divided solid and the protective layer be formed by fusing the solid particles to a continuous coating at a suitable temperature.
- the protective agent may also be emulsified or dispersed in a liquid which is not a true solvent and applied to metal surfaces in this form, with the evaporation of the carrier. occurring subsequently. In some instances it has; been found that oils of various types may serve as carriers for the protective agent, and in such cases it is not intended that the carrier be removed by evaporation as is the practice when solvents or dispersions are used.
- thefilm or layer of anti-corrosive deposited on the metal surface be .of such thickness that one pound will coat approximately 20,000 square feet. of metal.
- a film of about this thickness may. readily be obtained by dipping the metal into a 4% solution of the protective agent. Films of a thickness such that one pound will coat approximately 10,000 square feet or of a thickness such that one pound will coat approximately 80,000, square feet may also, but less preferably, be used. These thicknesses may be obtained by dipping a sheet of steel into 8% and 1% solutions of the agents, respectively.
- metallic cases, etc. and to the treatment of fer rous metal articles which havebeen provided with a surface coating of some other metal or alloy, such as chromium, copper, nickel, cadmium, zinc, brass, aluminum, tin, lead, etc.
- these compounds may be applied to the surfaces of other metals andalloys, particularly those used for structural shapes and articles of commerce such as rods,'tubes and sheets.
- metals are zinc, brass, bronze, aluminum, tin, copper, pewter, lead, magnesium, cadmium,
- a process for the prevention of iron oxidation which comprises treating the area susceptible oxidation with a long chain amine salt of orthophosphoric acid, said long chain being a hydrocarbon chain.
- a process for the prevention of iron oxidation which comprises treating the area susceptible to oxidation with a long chain alkylammonium dihydrogen phosphate.
- Asian. article of manufacture a body having a metal surfaeesusceptible to atmospheric corrosion, at leasta part'cf which surface is coated with a" long chain amine salt of ortho-phoaphoric acid, said long chain-beings hydrocarbon elm.
- I I I I I I I i I 7 As an article of manufacture a body having a surface susceptibleto iron oxidation, at leasta part of whichsurface is-coated with a long chain amine salt of ortho-phosphoric acid, said long chain being a hydrocarbon chain.
- a body having a surface susceptible to iron oxidation at least a part of which surface is coated with a long chain amine salt of ortho-phosphoric acid, said long chain being a hydrocarbon chain and having superlmposedon at least a part of said coated surface a paint film.
- a body having a surface susceptible to iron oxidation at least a part of which surface is coated with a long chain alkylammonium dihydrogen phosphate and having superimposed on at least a part of said coated surface a paint film.
- a dodecylamine salt of ortho-phosphoric-acid i 12.
- the article of claim 11 characterized in that the said surface is coated with the salts deamine salt of ortho-phosphoric acid, said long 7 chain being a hydrocarbon chain.
- the article in accordance with claim l4 characterized in that the surface is coated with the mixture of alkyl amine salts obtained from ortho-phosphoric acid and the alkyl amines obtained by the catalytic hydrogenation of the nitriles derived from coconut oil fatty acids.
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Chemical Treatment Of Metals (AREA)
Description
Patented Mayll, 1943 coaaosron mnnn'rron Max T. Goebel, Lakewood. Ohio. and Isaac F.
Wilmingto Walker,
du Pont de Nemours a Company, DeL, a corporation of Delaware No Drawing. Application-Jnly 31,
Serial No. 404,832
15 Claims.
- This invention relates to corrosion inhibitors for metals and particularly to corrosion inhibitors which inhibit rust formation in ferrous metals occurring as the result of exposure to the effeet of moisture and oxygen.
It is well known that the surfaces of metals, particularly the surfaces of ferrous metals, normally tend to corrode with the formation of rust when subjected to the efi'ect of moisture and oxygen. Many methods have been proposed for preventing or inhibiting such corrosion and rust formation. One of the commonest methods proposed has comprised coating the metallic surfaces with a thin film of an oily material such as lanolin, vaseline, and similar materials. While such oily materials are to some extent effective, they have not proved to be entirely satisfactory in practice.
It is frequently desirable to app y to metal surfaces and particularly to ferrous metal surfaces lithographic inks, paints, lacquers, and the like. When the metal surfaces are preserved with oily materials, it is generally necessary to remove such oily materials from the metallic surfaces prior to application of lithographic inks, paints, lacquers and the like as such oily materials greatly decrease the receptivity of the metal surface for inks, paints, lacquers and the like.
It is an object of this invention to provide a new and improved method for the protection of metal surfaces from corrosion. Another object 'is to provide a new and improved method for the treatment of metallic surfaces so as to efiect the inhibiting of corrosion on the surface, and at the same time not decrease the receptivity of the surn,Del.,orstoE.I.
tion containing a phosphoric acid salt of a long chain aliphatic amine having at least one long chain aliphatic group of at least 8 carbon atoms attached directly to the amino nitrogen. These otherwise designated as those derived from a hydrogen orthophos'phate, for example or liophosface for lithographic inks, paints, and the like.
Another object is to provide a new and improved process for the treatment of ferrous metal surfaces so as to prevent the rusting of same. Another object is to provide new articles of commerce. A still further object is to develop corrosion inhibitors for ferrous metals which can be applied from simple aqueous systems. Another object is the treatment of ferrous metal surfaces to prevent their corrosion and further to prepare same for subsequent painting. Another object is to provide an improved process for painting. A further obiect'is to provide metals and particularly ferrous/metals, the surfaces of which will have a lesser tendency to be corroded and rusted. and which atthe same time will have a high receptivity for lithographic inks, paints, lacquers ,and the like. Another object is to provide certain new and useful compositions of matter and new articles of manufacture. Other objects will be apparent from the following description of the. invention- 1 These objects are accomplished by coating the surfaces of metals and particularly the surfaces offerrousmetalswlthathinfilmofacomposiphoric acid or a mono or dihydrogen phosphate, and a primary, secondary or tertiary amine having at least one long chain group of at least 8 carbon atoms attached directly to the aminonitrogen. The amine phosphates-. may also be obtained by reacting in the presence of water the salt of an aliphatic amine having at least one long chain group attached directly to the-amino nitrogen with a water soluble metallic salt of orthophosphoric acid. The phosphates formed may be either acid or neutral salts.
These phosphates when separated have been found to be exceptionally useful compounds. When applied to metal surfaces and particularly ferrous metal surfaces they have been found to have a marked rust-proofing effect. Furthermore, the surface becomes more receptive to paint film and paint films applied directly thereon adhere very well to the metal. The prosphates form colloidal solutions in water at elevated temperatures and may be used-in this form for treating the metal surfaces.
The following examples set forth certain well defined instances of the application of this invention. They are not, however, to be considered as limitations thereof since many modifications may I be made without departing from the spirit and scope of this invention. Examples I and II illustrate the method of preparing the compounds used in this invention. In these examples .the parts given are parts by weight. The remaining examples illustrate the treatment of metallic surfaces so as to provide the improvements obtained by the use of this invention.
Example I Two hundred parts of the mixture of alkyl amines obtainable by catalytically hydrogenating the nitriles derived from coconut oil fatty acids are added with stirring over a period of to minutes to 375 parts of 28.4% aqueous solution of HaPO4. The temperature is maintained at between and 0. during-the addition of the amine to the phosphoric acid solution. The reaction goes to completion in a short time, after which the mixture is chilled and filtered with pressure. The acid salt obtained in this way is washed with cold water and dried in an oven at 'ouite soft (grease-like) a 100! c. It
tially insoluble in coldvwater but at 100 0. water dissolves three-tenthsiits weight of the product readily. The product is insoluble, hot or cold,
in carbon tetrachloride, ethyl acetate, toluene or dioxan, butis soluble, hot or cold, in methanol.
Example II mm? v I deceny'l, hexadecenyl and octadecenylamine are also suitable.- Technicalmixtures are sometimes -.-used, as for example amines which" correspond Two hundred parts of n dodecylamine m added with stirring to 312 parts Ma 17% aqueous solution of H3904. The reaction goes to completion in a short time after which the phosphate is separated by filtration and is then dried.
Example HI Twenty-gauge steel sheet, free from rust and grease, was dipped in a hot. 1:1 ethyl alcoholwater solution containing 4% hexadecylammonium dihydrogen phosphate and then chewed to dry in the open air. Steel panels so treated were exposed outdoors along with similar steel panels similarly treated with other commonly used protective materials. are collected in the following table:
Rating lO-no visible rust; O-suriace' covered completely with ust.
Example IV Steel sheet which was first phosphatized by the usual process known as Bonderiting, whereby a definite layer of iron phosphate is produced on the surface, and then sprayed with 4% octadecylamine in toluene solution was exposed out-ofdoors for three months. At the end of this period this treated 'steel was entirely rust-free, while steel sheet which had been similarly phosphatized but treated with light mineral oil was rusted heavily. Sheet which received no treatment subsequent to phosphatlzing was covered with rust over its entire surface.
Example V A brass sheet which had been freed of dirt and grease was treated by dipping the sheet in a 4% aqueous solution of dodecyl ammonium dihydrogen phosphate maintained at 90 C. The sheet after treatment had a pleasing satin finish. The treated sheet and similar untreated sheets were exposed to an industrial atmosphere indoors for a month. At the end of this period, the untreated sheets were badly tarnished while the treated sheets possessed their original pleasing appearance.
The amines which are useful in making the products of this invention may be classed as the long-chain aliphatic amines having said aliphatic group attached directly to the amino nitrogen atom, particularly those amines having at least tetradecyl, hexadecyl and octadecyl respectively to the alkylalcohols obtained by the catalytic hydrogenation of coconut oil acids and sperm oil; Monoamines having atleast one long chainvof less than twenty-five c'arbonatoms attached directly to the amino nitrogen atom are preferred because of availability and cost considerations, and monoamines containing at least one chain of from eight to eighteen carbon atoms attached directly to the amino nitrogen atom are particularly well suited to most of the applications where these products find use.
Phosphoric acid salts of alkylamines having a hydrocarbon chain of from 8 to 18 carbon atoms attached directly to the amino nitrogen have been found to be particularly useful in the following The results of this exposure instances: (1) The treatment of steel subjected to high humidity and the corrosive action of perspiration, for example, during the'handling of steel during fabrication, inspection, and packing; (2) the treatment of steel requiring temporary protection during exposure to weathering: (3) the treatment of plated iron or steel articles which may be subject to corrosion due to plating defects.
The following types of long-chain aliphatic ammonium phosphates having said aliphatic group attached directly to the amino nitrogen come within the scope of this invention:
Monoalkylammonium dihydrogen phosphates Monoalkylammonlum monohydrogen phosphates Y 12 methoxyoctadecylammonium that can be used, and amines containing an unsaturated chain such as octenyl, decenyl, do-
Neutral monoalkylammonium phosp s Dialkylammomum dihydrogen phosp ates Dialkylammonium monohydrogen phosphates Neutral dialkylammonium phosphates Trialkylammonium dihydrogen phosphates Trialkylammonium monohydrogen phosphates Neutral trialkylammonium phosphates While it is preferred to employ the long chain amine phosphates in which the long chain group is an alkyl group of at least 8 carbon atoms this long chain group may be substituted with such substituents as halogen, hydroxy, nitro, alkoxy, carboxyl or ester groups. However, from the standpoint of cost and availability the compounds ,where the long chain aliphatic group is hydro-' carbon are preferred.
Compounds of these types are illustrated by the following:
Di-octadecylammonium monohydrogen phosphate Tri-octadecylammonium phosphate IZ-chIgo-octadecylammonium dihydrogen phospha 12 hydroxy octadecylammonium dihydrogen f phosphate Y dihydrogen phosphate 9,10-octadecenylammohi'um dihydrogen phosphate Ethyldecylammonium dihydrogen phosphate Di(dimethyldodecylammonium) phosphate Trl(ethylmethyloctylammonium) phosphate monohydrogen The' majority of the compounds enumerated above all fall under the general formula:
B! [n-n n" 1.11,?0.
RIH
wherev .1: may be 1, 2 or 3 -"+i!.= R=an aliphatic radical having 8 to 24. carbon atoms and connected directly'to the amino nitrogen through single bonded carbon, and
preferably is hydrocarbon R, R", and R'". are hydr gen or aliphatic radicals of 8 to 24 carbon atoms connected directly to the amino nitrogen through single bonded carbon and preferably are hydrocarbon.
The first two examples cited above describe the preparation of these substituted ammonium acid phosphates from phosphoric acid and free amine, but the phosphoric acid may be replaced by inorganic acid phosphates such as the mono or disodium compounds, the corresponding potassium or ammonium salts and even compounds of those heavymetals which form soluble salts with phos-' phoric acid and the halogen or other mineral acids. Inorganic acid phosphates do not react directly with the free amines to give the desired compounds, but must be used with salts of the amines, and the metal salts formed in this double decomposition should be soluble to facilitate separation from the precipitated phosphate. When prepared in this way the substituted ammonium phosphate is usually washed free of inorganic salts before drying, although this is not always essential.
Example IV illustrates the formation of the substituted ammonium phosphate on the surface metal by first forming a surface layer of metal phosphate and then applying the amine. Acidic gases of the atmosphere may take part in this reaction.
It has been indicated that fairly concentrated solutions and low temperatures are preferred to increase the yield of material obtained. In many cases, however, it is not necessary to isolate the product at all since it can be used in the original reaction medium, and under these circumstances temperature control offers no advantages.
The long-chain alkylammonlum dihydrogen phosphates are particularly useful as anticorrodents for ferrous metal surfaces. They are useful in protecting such surfaces as steel sheet, wire, tubing, and various manufactured articles. The
monohydrogen phosphates can likewise be used for these purposes, and as acid-accepting constituents of coating composition films. When the long-chain alkylammonium phosphates are applied in solution, the preferred concentration lies between 2 and 10%, respectively; however, solutions containing as low as 1% or up 'to of these compounds may sometimes be used. The lower alcohols such as ethanol and methanol may be used as solvents, but water heated to 60 C. or more is equally suitable in most cases. The choice of solvent must be made, however, with regard to physical properties of the particular alkylammonium phosphate which is to be used, since in general these compounds become more soluble in organic solvents and less soluble in water as the hydrocarbon content of the molecule increases.
Although these compounds willusually be applied to metal surfaces by means of a'solution using such well known processes as dipping,
sprayin wiping, and brushing, it will be desirable at times to use other methods of application. A material which melts at reasonably low temperatures and which undergoes no decomposition in the region of its melting point may be applied in the liquid form without a diluent of any kind, provided that the application of the material is so regulated that the final protective film conforms to the desired thickness limits. These compounds may also be applied to the metal surface as a finely divided solid and the protective layer be formed by fusing the solid particles to a continuous coating at a suitable temperature. The protective agent may also be emulsified or dispersed in a liquid which is not a true solvent and applied to metal surfaces in this form, with the evaporation of the carrier. occurring subsequently. In some instances it has; been found that oils of various types may serve as carriers for the protective agent, and in such cases it is not intended that the carrier be removed by evaporation as is the practice when solvents or dispersions are used.
Long-chain aliphatic amines are effective anticorrodents in themselves, as has been disclosed in the copending application of Clifford K. Sloan, filed May 13, 1939, Serial No. 273,578, and it is well known from the prior art that phosphoric acid is a rust-proofing agent. However, the products disclosed in this invention do more than merely combine the properties of these two compounds for these products contain certain new and valuable properties which are not found in either the long-chain amines or in phosphoric acid.. For example, the amines alone have an adverse effect on adhesion of subsequently applied paint films, and phosphoric acid also tends to weaken the bond between paint and metal. Paints adhere very well to metal coated with the acid salts of thi invention, however, and such metal is not only protected effectively against corrosion during long periods of storage but can be painted over directly without any preliminary cleaning treatment. This property of the acid salts distinguishes them from ordinary protective films of oil and grease which must be removed completely before paint can be applied.
When a. paint film is subsequently to be applied to the metal surface, it is preferred that thefilm or layer of anti-corrosive deposited on the metal surface be .of such thickness that one pound will coat approximately 20,000 square feet. of metal. A film of about this thickness may. readily be obtained by dipping the metal into a 4% solution of the protective agent. Films of a thickness such that one pound will coat approximately 10,000 square feet or of a thickness such that one pound will coat approximately 80,000, square feet may also, but less preferably, be used. These thicknesses may be obtained by dipping a sheet of steel into 8% and 1% solutions of the agents, respectively.
Another-advantage of the compounds described herein is the absence of excessive reactivity. Phosphoric acid alone is too reactive to be used in the protection of zinc and cadmium plated metals, and it will also attack copper plate and produce objectionable discoloration. A longadded'em nd nmsny w s requires special I precautions because of theilrehazard.
' These compounds are particularly well adapted to the protection of ferrous metal articles, ,such
coating said metal surface-with a long cannuas bolts, nuts, nails, wire, sheets, tools, fine machine'ry parts, bearings, cutlery. sears, fire arms,
metallic cases, etc., and to the treatment of fer rous metal articles which havebeen provided with a surface coating of some other metal or alloy, such as chromium, copper, nickel, cadmium, zinc, brass, aluminum, tin, lead, etc. In addition to such uses, these compounds may be applied to the surfaces of other metals andalloys, particularly those used for structural shapes and articles of commerce such as rods,'tubes and sheets. Among such metals are zinc, brass, bronze, aluminum, tin, copper, pewter, lead, magnesium, cadmium,
"duralumin, nickel, etc.
This application is a continuation-in-part of our copending application Serial No. 273,580, filed May 13, 1939. 1
It is apparent that many widely different embodiments of this invention may be made with out departing from the spirit and scope'thereof and therefore it is not intended to be limited except as indicated in the appended claims.
We claim:
1. The process for the prevention of atmospheric corrosion of metal surfaces capable of. corrosion, which comprises treating, the said surfaces with a long chain amine salt of ortho-phos phoric acid, said long chain being a hydrocarbon chain.
2. A process for the prevention of iron oxidation which comprises treating the area susceptible oxidation with a long chain amine salt of orthophosphoric acid, said long chain being a hydrocarbon chain.
3. A process for the prevention of iron oxidation which comprises treating the area susceptible to oxidation with a long chain alkylammonium dihydrogen phosphate.
4. In a process of painting metal surfaces comprising the steps of treating said metal surfaces to clean and prepare same for the reception of the paint film, the improvement which comprises coating said metal surface with a long chain kylammcnium dihydrogen phosphate. e
6. Asian. article of manufacture a body having a metal surfaeesusceptible to atmospheric corrosion, at leasta part'cf which surface is coated with a" long chain amine salt of ortho-phoaphoric acid, said long chain-beings hydrocarbon elm. I I I I I I i I 7. As an article of manufacture a body having a surface susceptibleto iron oxidation, at leasta part of whichsurface is-coated with a long chain amine salt of ortho-phosphoric acid, said long chain being a hydrocarbon chain.
8. A; anarticle of manufacture a body having a surfacev susceptible to iron oxidation, at least a part of which surface is coated with a long chain alkylammonium dihydrosen phosphate.
9. As an article of manufacture a body having a surface susceptible to iron oxidation, at least a part of which surface is coated with a long chain amine salt of ortho-phosphoric acid, said long chain being a hydrocarbon chain and having superlmposedon at least a part of said coated surface a paint film.
10. As an article of manufacture a body having a surface susceptible to iron oxidation, at least a part of which surface is coated with a long chain alkylammonium dihydrogen phosphate and having superimposed on at least a part of said coated surface a paint film.-
11. As an article of manufacture, a body having -a metal surface susceptible to atmospheric corrosion and containing copper, at least a part of I which surface is coated with a dodecylamine salt of ortho-phosphoric-acid. i 12. The article of claim 11 characterized in that the said surface is coated with the salts deamine salt of ortho-phosphoric acid, said long 7 chain being a hydrocarbon chain.
5. In a process of'painting metal surfaces comprising the-st'eps of treating said metal surfaces to clean and prepare same for the reception of the paint film, the improvement which comprises 15. The article in accordance with claim l4 characterized in that the surface is coated with the mixture of alkyl amine salts obtained from ortho-phosphoric acid and the alkyl amines obtained by the catalytic hydrogenation of the nitriles derived from coconut oil fatty acids.
MAX T. GOEBEL. ISAAC F. WALKER.
Priority Applications (1)
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US404832A US2318606A (en) | 1941-07-31 | 1941-07-31 | Corrosion inhibition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US404832A US2318606A (en) | 1941-07-31 | 1941-07-31 | Corrosion inhibition |
Publications (1)
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US2318606A true US2318606A (en) | 1943-05-11 |
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ID=23601241
Family Applications (1)
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US404832A Expired - Lifetime US2318606A (en) | 1941-07-31 | 1941-07-31 | Corrosion inhibition |
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Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419327A (en) * | 1943-06-28 | 1947-04-22 | Shell Dev | Corrosion inhibitors-nitrite salts of secondary amines |
US2562549A (en) * | 1945-10-17 | 1951-07-31 | Hall Lab Inc | Treatment of steam systems |
US2692840A (en) * | 1951-11-19 | 1954-10-26 | Parker Rust Proof Co | Single package primary chemical treatment composition |
US2737498A (en) * | 1946-07-12 | 1956-03-06 | Produits Chim Terres Rares Soc | Product for and process of treating metallic articles before coating |
US2758949A (en) * | 1951-06-28 | 1956-08-14 | Parker Rust Proof Co | Alkali metal phosphate coating solutions and the method of forming coatings therewith |
US2766154A (en) * | 1952-03-26 | 1956-10-09 | Parker Rust Proof Co | Method of coating metals with amine phosphate coating and composition therefor |
US2769737A (en) * | 1952-03-26 | 1956-11-06 | Parker Rust Proof Co | Amine phosphate coating solutions and method of coating |
US2811456A (en) * | 1955-02-28 | 1957-10-29 | Victor Chemical Works | Protective film for ferrous metals |
US2828233A (en) * | 1953-10-07 | 1958-03-25 | William P Langworthy | Coating and annealing process for magnetic materials and coated article produced thereby |
US2837449A (en) * | 1952-08-14 | 1958-06-03 | Henkel & Cie Gmbh | Composition of matter for and process of producing phosphate layers on iron surfaces |
US2838417A (en) * | 1954-09-28 | 1958-06-10 | Dow Chemical Co | Acidizing industrial equipment |
US2917481A (en) * | 1953-08-27 | 1959-12-15 | American Can Co | Coating composition containing phenol aldehyde condensation product, vinyl polymer, catalyst, amine phosphate and heavy metal salt |
US2936289A (en) * | 1955-05-05 | 1960-05-10 | Olin Mathieson | Water treating composition |
US2992145A (en) * | 1960-01-20 | 1961-07-11 | Quaker Chemical Products Corp | Compositions for simultaneously phosphating and lubricating ferrous metals |
US3129121A (en) * | 1962-04-04 | 1964-04-14 | Amchem Prod | Phosphate coating solution and method of coating ferriferous metal |
US3197344A (en) * | 1962-04-23 | 1965-07-27 | Hooker Chemical Corp | Compositions and methods for forming coatings on metal surfaces |
US4253886A (en) * | 1974-11-21 | 1981-03-03 | Fuji Photo Film Co., Ltd. | Corrosion resistant ferromagnetic metal powders and method of preparing the same |
-
1941
- 1941-07-31 US US404832A patent/US2318606A/en not_active Expired - Lifetime
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2419327A (en) * | 1943-06-28 | 1947-04-22 | Shell Dev | Corrosion inhibitors-nitrite salts of secondary amines |
US2562549A (en) * | 1945-10-17 | 1951-07-31 | Hall Lab Inc | Treatment of steam systems |
US2737498A (en) * | 1946-07-12 | 1956-03-06 | Produits Chim Terres Rares Soc | Product for and process of treating metallic articles before coating |
US2758949A (en) * | 1951-06-28 | 1956-08-14 | Parker Rust Proof Co | Alkali metal phosphate coating solutions and the method of forming coatings therewith |
US2692840A (en) * | 1951-11-19 | 1954-10-26 | Parker Rust Proof Co | Single package primary chemical treatment composition |
US2766154A (en) * | 1952-03-26 | 1956-10-09 | Parker Rust Proof Co | Method of coating metals with amine phosphate coating and composition therefor |
US2769737A (en) * | 1952-03-26 | 1956-11-06 | Parker Rust Proof Co | Amine phosphate coating solutions and method of coating |
US2837449A (en) * | 1952-08-14 | 1958-06-03 | Henkel & Cie Gmbh | Composition of matter for and process of producing phosphate layers on iron surfaces |
US2917481A (en) * | 1953-08-27 | 1959-12-15 | American Can Co | Coating composition containing phenol aldehyde condensation product, vinyl polymer, catalyst, amine phosphate and heavy metal salt |
US2828233A (en) * | 1953-10-07 | 1958-03-25 | William P Langworthy | Coating and annealing process for magnetic materials and coated article produced thereby |
US2838417A (en) * | 1954-09-28 | 1958-06-10 | Dow Chemical Co | Acidizing industrial equipment |
US2811456A (en) * | 1955-02-28 | 1957-10-29 | Victor Chemical Works | Protective film for ferrous metals |
US2936289A (en) * | 1955-05-05 | 1960-05-10 | Olin Mathieson | Water treating composition |
US2992145A (en) * | 1960-01-20 | 1961-07-11 | Quaker Chemical Products Corp | Compositions for simultaneously phosphating and lubricating ferrous metals |
US3129121A (en) * | 1962-04-04 | 1964-04-14 | Amchem Prod | Phosphate coating solution and method of coating ferriferous metal |
US3197344A (en) * | 1962-04-23 | 1965-07-27 | Hooker Chemical Corp | Compositions and methods for forming coatings on metal surfaces |
US4253886A (en) * | 1974-11-21 | 1981-03-03 | Fuji Photo Film Co., Ltd. | Corrosion resistant ferromagnetic metal powders and method of preparing the same |
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