US2275223A - Rustproof material and process - Google Patents
Rustproof material and process Download PDFInfo
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- US2275223A US2275223A US106615A US10661536A US2275223A US 2275223 A US2275223 A US 2275223A US 106615 A US106615 A US 106615A US 10661536 A US10661536 A US 10661536A US 2275223 A US2275223 A US 2275223A
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- magnetite
- iron
- oxide
- copper
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- 238000000034 method Methods 0.000 title description 26
- 239000000463 material Substances 0.000 title description 7
- 230000008569 process Effects 0.000 title description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 80
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 45
- 229910052742 iron Inorganic materials 0.000 description 40
- 229910052751 metal Inorganic materials 0.000 description 32
- 239000002184 metal Substances 0.000 description 32
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 26
- 229910052802 copper Inorganic materials 0.000 description 26
- 239000010949 copper Substances 0.000 description 26
- 239000011248 coating agent Substances 0.000 description 25
- 238000000576 coating method Methods 0.000 description 25
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 20
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 17
- 229910052804 chromium Inorganic materials 0.000 description 17
- 239000011651 chromium Substances 0.000 description 17
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical group [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 15
- 238000005260 corrosion Methods 0.000 description 14
- 230000007797 corrosion Effects 0.000 description 14
- 150000002739 metals Chemical class 0.000 description 13
- 229910000831 Steel Inorganic materials 0.000 description 12
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 12
- 239000011133 lead Substances 0.000 description 12
- 239000010959 steel Substances 0.000 description 12
- 239000011135 tin Substances 0.000 description 12
- 229910052718 tin Inorganic materials 0.000 description 12
- 239000011701 zinc Substances 0.000 description 12
- 229910052725 zinc Inorganic materials 0.000 description 12
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 11
- 239000003513 alkali Substances 0.000 description 11
- 229910052759 nickel Inorganic materials 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 9
- 239000002131 composite material Substances 0.000 description 8
- 238000004519 manufacturing process Methods 0.000 description 7
- 230000009471 action Effects 0.000 description 5
- 230000001464 adherent effect Effects 0.000 description 5
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000003518 caustics Substances 0.000 description 3
- 238000000151 deposition Methods 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 230000001681 protective effect Effects 0.000 description 3
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- -1 chormium Chemical compound 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 229960004887 ferric hydroxide Drugs 0.000 description 2
- IEECXTSVVFWGSE-UHFFFAOYSA-M iron(3+);oxygen(2-);hydroxide Chemical compound [OH-].[O-2].[Fe+3] IEECXTSVVFWGSE-UHFFFAOYSA-M 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 229910016516 CuFe2O4 Inorganic materials 0.000 description 1
- 229910000604 Ferrochrome Inorganic materials 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 241000006770 Xenia Species 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HODFCFXCOMKRCG-UHFFFAOYSA-N bitolterol mesylate Chemical compound CS([O-])(=O)=O.C1=CC(C)=CC=C1C(=O)OC1=CC=C(C(O)C[NH2+]C(C)(C)C)C=C1OC(=O)C1=CC=C(C)C=C1 HODFCFXCOMKRCG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- DXKGMXNZSJMWAF-UHFFFAOYSA-N copper;oxido(oxo)iron Chemical compound [Cu+2].[O-][Fe]=O.[O-][Fe]=O DXKGMXNZSJMWAF-UHFFFAOYSA-N 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000002848 electrochemical method Methods 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 229940037395 electrolytes Drugs 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011872 intimate mixture Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- ZAUUZASCMSWKGX-UHFFFAOYSA-N manganese nickel Chemical compound [Mn].[Ni] ZAUUZASCMSWKGX-UHFFFAOYSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003112 potassium compounds Chemical class 0.000 description 1
- UMPKMCDVBZFQOK-UHFFFAOYSA-N potassium;iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[K+].[Fe+3] UMPKMCDVBZFQOK-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- GMMAPXRGRVJYJY-UHFFFAOYSA-J tetrasodium 4-acetamido-5-hydroxy-6-[[7-sulfonato-4-[(4-sulfonatophenyl)diazenyl]naphthalen-1-yl]diazenyl]naphthalene-1,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].OC1=C2C(NC(=O)C)=CC=C(S([O-])(=O)=O)C2=CC(S([O-])(=O)=O)=C1N=NC(C1=CC(=CC=C11)S([O-])(=O)=O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 GMMAPXRGRVJYJY-UHFFFAOYSA-J 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D9/00—Electrolytic coating other than with metals
- C25D9/04—Electrolytic coating other than with metals with inorganic materials
- C25D9/08—Electrolytic coating other than with metals with inorganic materials by cathodic processes
- C25D9/10—Electrolytic coating other than with metals with inorganic materials by cathodic processes on iron or steel
Definitions
- This invention comprises as a rustproofing material for iron and steel articles an artificial mineralogical analogue of magnetite which affords a corrosion protective surface of pleasing color and attractive appearance and the herein described electrochemical process of producing various artificial magnetite V analogues.
- the object of the invention is to produce upon iron and steel articles a protective surface finish which is impervious and strongly resistant to corrosion or rust, and which affords a pleasing color and attractive appearance.
- a further and highly important object of the invention is the production of mineralogical analogues of magnetite by electrochemical process.
- a further object of the invention isthe control of production and deposit of mineralogical analogues of magnetite.
- a further object of the invention is the homogeneous combination of a magnetite analogue with an iron or steel article as a surface finish thereon.
- a further object of the invention is to provide an impervious protective surface finish of great durability.
- a further object 'of the invention is the use of mineralogical analogues of magnetite as a rustproofing and corrosion resistant material.
- a further but none the less important object of the invention is to provide a practical commercially operable method of artificial productionof various magnetite analogues.
- the invention consists in the use of various mineralogical analogues of magnetite as rustproofing and corrosion resistant materials, 'and in the herein described processof artificial production of various magnetite analogues and their surface deposit upon iron and steel articles.
- the present rustproofing material and its production includes the formation by electrochemical action on iron and steel surfaces of a double oxide of iron and some other metal, for example copper, lead, tin, chromium, zinc, manganese, or nickel, thereby effecting an artificial analogue of magnetite (F6304) wherein monoxides of either of the aforementioned metals are substituted for FeO.
- FeO copper magnetite
- the process may be carried out in different ways, preferably however as the simultaneous deposit of the :two metals in a single solution.
- the steps of the preferred method comprise use solution then comprises a mixture of sodium ferrite, ferric hydroxide, and sodium hydroxide.
- the mixture will contain correspondingly potassium compounds.
- An anode of the desired nonferrous material (copper, chromium, lead, tin, zinc, manganese nickel) is suspended inthe solution and the iron or steel article to be treated is suspended therein as the cathode.
- a tightly adherent impervious coating of high corrosive resistance and pleasing appearance forms upon the article (cathode) which chemical analysis shows to be an oxide film of both iron and the particular metal employed as the proportionate to the surface area being coated in square decimeters, and second, the concentration of the solution.
- the deposit becomes coarse, granular and but loosely adherent. If the current density is materially reduced, the rate of deposit becomes too slow'for practical commercial operation.
- the cathodic deposit of an oxide is believed to result from production of colloid hydroxides which are electro-positive colloids by the electrolytic corrosion of the anodes, and which migrate under suitable potential gradient to the cathode where they are reduced by nascent hydrogen to the oxide state.
- these oxides show such marked ailinity for the surface molecules of an iron bodypossessing negative polarity as to tenaciously attach themselves to the surface of even a smooth polished article so as to produce not a mere smudge, but a continuous tightly adherent corrosion resistant coating of appreciable depth, is yet not definitely known.
- the steps as described do produce such result which is amply suflicient for the present disclosure.
- the artificial chrome-magnetite in addition to the advantage of insolubility of chromite possesses a beautiful blue black color which enhances the appearance and increases the saleabllity of tools and other articles to which the finish may be applied.
- Such magnetite analogue appears to be formed in the surfacematerial of the article of which it becomes a homogeneous component and does not add appreciably to the weight thereof and is inseparable therefrom.
- a metallic article including a double oxide coating of rustproof material comprising a cathodic composite coating of an oxide of iron combined in intimate mixture with an oxide of a a metal selected from a group of at least two of the metals specified.
- An electrochemically deposited artificial mineralogical analogue) of magnetite comprising an oxide of iron chemically combined with an oxide of copper.
- a metallic article and a surface covering therefor of electrochemically deposited artificial mineralogical analogue of magnetite comprising an oxide of iron chemically combined with an oxide of chromium.
- a metallic article and a surface covering therefor of electrochemically deposited artificial mineralogical analogue of magnetite comprising an oxide of iron chemically combined with an oxide of a metal selected from agroup of at least two of the metals specified.
- ing iron or steel articles including the steps of providing an alkali bath of approximately twenty to twenty-five per cent concentration adding iron in solution to the bath, suspending therein as a cathode an iron or steel article to be treated, and
- an anode of a metal selected from a group of metals consisting of copper, chromium, tin, zinc, manganesanickel and lead and circulating electric current tlierebetween of approximately three and a half amperes per square decimeter of surface to be coated whereby there is deposited upon the cathode article a magnetite analogue of the anode metal.
- the herein described method of effectin electrochemical deposit of a magnetite analogue including preparing a ferric hydroxide alkali electrolytic' solution of approximately twenty to twenty-five per cent concentration, and subjecting thereto a ferrous cathode and an anode element selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel and lead, and circulating an electric current therethrough having a density of approximately three and a half amperes per square decimeter whereby there is effected upon the cathode element a deposit of a magnetite analogue of the anode metal.
- the herein described method consisting of providing a caustic alkali solution, electrolytically introducing iron in solution therein, suspending therein a ferrous cathode and a copper anode, circulating electric current of approximately cathodic surface through the solution between the anode and cathode whereby a copper magnetite deposit will be produced upon the cathode.
- the herein described method consisting of providing a caustic alkali solution inducing electrolysis between iron electrodes suspended in the solution, suspending therein a ferrous cathode and a chromium anode, circulating electric current of approximately three and a half amperes per square decimeter of cathode surface through the solution between the anode and cathode whereby a chromium magnetite deposit will be manganese, nickel and lead, and circulating therethrough an electric current of ample density to effect simultaneous electrochemical deposits of an oxide of iron and an oxide of the selected metal, the steps and procedure being such as to unify the deposits into a composite magnetite analogue.
- the herein described method of providing a corrosion resistant coating including electrochemically depositing upon a cathodic article simultaneously deposits of an oxide of iron and an oxide of copper and thereby forming a composite coating of copper magnetite.
- the herein described method of providing a corrosion resistant coating including simultaneously electrochemically depositing upon a cathodic article containing iron deposits of an oxide of iron and an oxide of chromium in the form of a composite coating of chromium magnetite.
- a metallic article and a rustprooflng coating therefor comprising an artificial analogue of magnetite.
- a metallic article and a rustproofing coating therefor comprising a unified combination of oxides of iron and of a metal select'ed from a group consisting of copper, chromium, tin,'zinc, manganese, nickel and lead.
- a metallic article and a rust proof coating therefor comprising an electrochemical cathodic deposit of analogue of magnetite.
- a metallic article and a rustproofing coating cent concentration wherein the anode is of a metal selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel and lead and maintaining therein a current density of substantially three and a half amperes per square decimeter of cathodic surface whereby there is deposited upon the cathodic surface a magnetite analogue of the anodic metal.
- the herein described method offorming a double oxide coating upon a ferrous article including the steps of utilizing the ferrous article to be coated as the cathode in a caustic soda solution having a concentration of approximately twenty to twenty-five per cent by weight and three anda half amperes per square decimeter of employing therein a copper anode, and circulating electric current between said elements through the bath at a' current density of approximately three and a half amperes persquare decimeter to effect on the ferrous article simultaneous cathodic deposits of oxide of iron and' oxide of copper.
- the herein described method of forming a double oxide coating upon a ferrous article including temporarily utilizing the ferrous article to be coated as a cathode element in an alkali electrolytic bath, simultaneously employing thereinan anode element containing copper and passing electric current between the elements through the electrolytic bath at a current density of approximately three and a half amperes per square decimeter of surface to be coated, thereby ef-' fecting upon the surface of the article a cathodic deposit of cupro-magnetite.
- the herein described method of forming a double oxide coating upon a ferrous article including temporarily utilizing the ferrous article to be coated as a cathode element in an alkali electrolytic bath, simultaneously employing therein an anode element containing chromium and passing electric current between the elements through the electrolytic bath at a current density of approximately three and. a half amperes'per square decimeter of surface to be coated, thereby efiecting upon the surface of the article a cathodic deposit of chromite.
- the herein described method of producing an analogueof magnetite including charging an alkali electrolytic bath of approximately twenty to twenty-five per cent concentration with iron.
- anodic element selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel, and lead, and a cathodic element of iron .or steel, and circulating through such bath an electric current having a density of approximately three and a' half amperes per square decimeter of cathodic surface whereby there will be deposited upon the cathodic element double oxide of iron and the selected anodic metal.
- the herein described method of producing an analogue of magnetite including the step of utilizing an alkali electrolytic bath of approximately twenty to twenty-five per cent concentration, circulating an electric current through said bath between iron electrodes until the specific gravity of the solution is increased from two and a half to seven per cent, employing in said-bath an anodic element selected from a group of metals consisting of copper, chormium, tin, zinc, manganese, nickel, and lead, and a cathodic element of iron or steel, and circulating through such bath an electric current having a density of approximately three and a half amperes per square decimeter of cathodic surface whereby there will be deposited upon the cathodic element double oxideof iron and the selected anodic metal.
- the herein described method of producing copper magnetite including charging an alkali electrolytic bath 'of approximately twenty to twenty-five per cent concentration with iron by v electrolysis between iron electrodes until the speciiic gravity of the bath has been increased two circulating therebetween an electric current having a density of approximately three and a half amperes per square decimeter of cathodic. surface whereby there is deposited upon thecathodic element a double oxide of iron and copper.
- the method of providing a corrosion resistant coating upon an article which consists in providing a caustic alkali solution, electrolytically introducing iron in solution therein, suspending a ferrous cathode and a non-ferrous anode of a metal selected from a group comprising copper, chromium, tin, zinc, manganese, nickel and lead. and passing an electrical current through the solution between the anode and cathode whereby there is obtained a composite coating upon the cathode of an oxide of iron chemically combined with an oxide of one of the non-ferrous metals used as the anode.
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Electroplating Methods And Accessories (AREA)
Description
Patented Mar. 3, 1942 Robert H. Hardoen, Xenia, Ohio No Drawing. Application October 20, 1936, Serial No. 106,615
26 Claims.
This invention comprises as a rustproofing material for iron and steel articles an artificial mineralogical analogue of magnetite which affords a corrosion protective surface of pleasing color and attractive appearance and the herein described electrochemical process of producing various artificial magnetite V analogues.
It has long been common practice to apply magnetite (F6304) by electrodeposit wherein the articles are used as anodes in an electrolytic bath of relatively high temperature thereby producing a black adherent coating which affords a considerable degree of protection against atmospheric corrosion. Such methods are not only expensive, but may alter the physical characteristics of the metal being treated, and the developed coating of magnetite contains impurities in exposed pores which afford points of corrosion attack and have necessitated the addition of an oil or lacquer treatment to render such coating alogical formula CuQFezOa and chrome-magnetite having chemical formula CrzFeOr and mineralogical formula CI'2O3.FeO. It is said that a French scientist, Henri Moisson, succeeded by thermal methods in laboratory experimental production of a number of analogues of magnetite by substituting monoxides of several different metals for FeO in the mineralogical'formula, but
, such magnetite analogues heretofore never have been artificially produced by electrochemical methods as herein described, and never have been commercially produced by any means nor the production thereof usably controlled.
The object of the invention is to produce upon iron and steel articles a protective surface finish which is impervious and strongly resistant to corrosion or rust, and which affords a pleasing color and attractive appearance.
A further and highly important object of the invention is the production of mineralogical analogues of magnetite by electrochemical process.
A further object of the invention isthe control of production and deposit of mineralogical analogues of magnetite.
A further object of the invention is the homogeneous combination of a magnetite analogue with an iron or steel article as a surface finish thereon.
A further object of the invention is to provide an impervious protective surface finish of great durability.
A further object 'of the invention is the use of mineralogical analogues of magnetite as a rustproofing and corrosion resistant material.
A further but none the less important object of the invention is to provide a practical commercially operable method of artificial productionof various magnetite analogues.
with the above primary and other incidental ob ects in view as will more fully appear in the specification, the invention consists in the use of various mineralogical analogues of magnetite as rustproofing and corrosion resistant materials, 'and in the herein described processof artificial production of various magnetite analogues and their surface deposit upon iron and steel articles.
The present rustproofing material and its production includes the formation by electrochemical action on iron and steel surfaces of a double oxide of iron and some other metal, for example copper, lead, tin, chromium, zinc, manganese, or nickel, thereby effecting an artificial analogue of magnetite (F6304) wherein monoxides of either of the aforementioned metals are substituted for FeO. Thus in producing copper magnetite (CuFe2O4) CuO replaces FeO.
The process may be carried out in different ways, preferably however as the simultaneous deposit of the :two metals in a single solution.
The steps of the preferred method comprise use solution then comprises a mixture of sodium ferrite, ferric hydroxide, and sodium hydroxide.
If potassium is used, the mixture will contain correspondingly potassium compounds.
An anode of the desired nonferrous material (copper, chromium, lead, tin, zinc, manganese nickel) is suspended inthe solution and the iron or steel article to be treated is suspended therein as the cathode. Upon circulation of current as in electroplating methods, at room temperature of approximately twenty to twenty-five degrees centigrade and with a current of approximately three and a half amperes per square decimeter, a tightly adherent impervious coating of high corrosive resistance and pleasing appearance forms upon the article (cathode) which chemical analysis shows to be an oxide film of both iron and the particular metal employed as the proportionate to the surface area being coated in square decimeters, and second, the concentration of the solution. If the current density is materially increased, as for example fifty percent above that of 3.5 amps./dm. mentioned, the deposit becomes coarse, granular and but loosely adherent. If the current density is materially reduced, the rate of deposit becomes too slow'for practical commercial operation.
It is also found that above and below the range R of solution concentration of 20-25% sodium hydroxide, the results rapidly become unsatisfactory.
It is not necessary that the scientific principle be explained nor even that it shall be known so long asthe process or mode of operation which produces the result is disclosed, hence any statements of theory or principle contained herein are explanation only and not with intent to limit the character, scope or application of the invention. The exact reactions induced in the present instance are not positively known. There apparently occurs at the cathode a reduction of sodium or potassium ferrate from the solution and a simultaneous deposit of cupric oxide or black oxide of copper, chromium oxide or analogous oxides of such other metals which may be used as the anode material which apparently combine-into a composite film oi cupro-magnetite, chromite,
, or other analog of magnetite, tightly adherent ing action and is of a grayish black color which becomes a brilliant black when lightly wiped with an oiled cloth.
The cathodic deposit of an oxide is believed to result from production of colloid hydroxides which are electro-positive colloids by the electrolytic corrosion of the anodes, and which migrate under suitable potential gradient to the cathode where they are reduced by nascent hydrogen to the oxide state. Just why these oxides show such marked ailinity for the surface molecules of an iron bodypossessing negative polarity as to tenaciously attach themselves to the surface of even a smooth polished article so as to produce not a mere smudge, but a continuous tightly adherent corrosion resistant coating of appreciable depth, is yet not definitely known. The steps as described do produce such result which is amply suflicient for the present disclosure. When a copper anode is employed the copper ions travelling through the bath become a part of the molecular structure of the surface coating of the iron or steel cathode article. Likewise when chromium or ferro-chromium is empoyed, analysis shows the presence of chromium in such coating.
In lieu of such composite deposition of ferrous upon the bare iron in accordance with the well known electromotive series and will thereby seal against corrosion at such exposed spot.
The artificial chrome-magnetite in addition to the advantage of insolubility of chromite possesses a beautiful blue black color which enhances the appearance and increases the saleabllity of tools and other articles to which the finish may be applied.
Extensive corrosion tests show that the complex oxide finish herein described is much more resistant to corrosion than ordinary magnetite.
Tests as to solubility, hardness, specific gravity,
and refractive indices, particularly upon those specimens which have been heat treated show that the artificial magnetite analogues forming the subject matter hereof approach quite closely to the natural minerals which they simulate.
Since it is not necessary nor essential that an inventor shall state or even know the theory or principle upon which his invention is dependent, and in view of the generally unsettled state of scientific opinion regarding the mechanism of electrochemical reactions in such complex elec-- trolytes, no explanation of such action is here attempted. working within the limits above mentioned and in the manner described, which have been stated for illustrative purposes only, and with no intent to unduly limit thescope or application of the invention, and employing an anode of nonferrous metal, there is eflected by electrochemical action upon a cathodic article of iron or steel an oxide coating containing iron in combination 'with the particular. metal used as the anode.
Such magnetite analogue appears to be formed in the surfacematerial of the article of which it becomes a homogeneous component and does not add appreciably to the weight thereof and is inseparable therefrom.
At present copper magnetite, tin magnetite and chromium magnetite have been found most eflicient and desirable for commercial purposes, but it is to be understood that the invention is not limited thereto, but includes other mineralogical analogues of magnetite of whichv lead, zinc, manganese and nickel have been mentioned as examples. Likewise while the simultaneous deposit of the dissimilar metals in a single solution is preferred, their separate deposit and subsequent unification by heat treatment into a composite coating of a magnetite analogue of such metals is also within the contemplated scope of this invention.
The deposit resulting for the described process occurs very rapidly in its initial stages and is gradually retarded as the surfaces are covered until after a short period of time, ordinarily ten It has been found, however, that to fifteen minutes under the temperature conditions, concentration of solution and amperage mentioned the action substantially ceases, af-
fordin'g, however, a very dense surface stratum copper, chromium, tin, zinc, manganese, nickel and lead.
3. A metallic article including a double oxide coating of rustproof material comprising a cathodic composite coating of an oxide of iron combined in intimate mixture with an oxide of a a metal selected from a group of at least two of the metals specified.
4. An electrochemically deposited artificial mineralogical analogue) of magnetite comprising an oxide of iron chemically combined with an oxide of copper.
5. A metallic article and a surface covering therefor of electrochemically deposited artificial mineralogical analogue of magnetite comprising an oxide of iron chemically combined with an oxide of chromium. f
6. A metallic article and a surface covering therefor of electrochemically deposited artificial mineralogical analogue of magnetite comprising an oxide of iron chemically combined with an oxide of a metal selected from agroup of at least two of the metals specified.
7. The herein described method of rustproofmetals consisting of copper, chromium, zinc, tin, v
ing iron or steel articles including the steps of providing an alkali bath of approximately twenty to twenty-five per cent concentration adding iron in solution to the bath, suspending therein as a cathode an iron or steel article to be treated, and
an anode of a metal selected from a group of metals consisting of copper, chromium, tin, zinc, manganesanickel and lead and circulating electric current tlierebetween of approximately three and a half amperes per square decimeter of surface to be coated whereby there is deposited upon the cathode article a magnetite analogue of the anode metal. I
8. The herein described method of effectin electrochemical deposit of a magnetite analogue including preparing a ferric hydroxide alkali electrolytic' solution of approximately twenty to twenty-five per cent concentration, and subjecting thereto a ferrous cathode and an anode element selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel and lead, and circulating an electric current therethrough having a density of approximately three and a half amperes per square decimeter whereby there is effected upon the cathode element a deposit of a magnetite analogue of the anode metal.
9.'The herein described method consisting of providing a caustic alkali solution, electrolytically introducing iron in solution therein, suspending therein a ferrous cathode and a copper anode, circulating electric current of approximately cathodic surface through the solution between the anode and cathode whereby a copper magnetite deposit will be produced upon the cathode.
10. The herein described method consisting of providing a caustic alkali solution inducing electrolysis between iron electrodes suspended in the solution, suspending therein a ferrous cathode and a chromium anode, circulating electric current of approximately three and a half amperes per square decimeter of cathode surface through the solution between the anode and cathode whereby a chromium magnetite deposit will be manganese, nickel and lead, and circulating therethrough an electric current of ample density to effect simultaneous electrochemical deposits of an oxide of iron and an oxide of the selected metal, the steps and procedure being such as to unify the deposits into a composite magnetite analogue.
12. The herein described method of providing a corrosion resistant coating including electrochemically depositing upon a cathodic article simultaneously deposits of an oxide of iron and an oxide of copper and thereby forming a composite coating of copper magnetite.
13. The herein described method of providing a corrosion resistant coating including simultaneously electrochemically depositing upon a cathodic article containing iron deposits of an oxide of iron and an oxide of chromium in the form of a composite coating of chromium magnetite.
14. A metallic article and a rustprooflng coating therefor comprising an artificial analogue of magnetite.
15. A metallic article and a rustproofing coating therefor comprising a unified combination of oxides of iron and of a metal select'ed from a group consisting of copper, chromium, tin,'zinc, manganese, nickel and lead.
16. A metallic article and a rust proof coating therefor comprising an electrochemical cathodic deposit of analogue of magnetite.
17. A metallic article and a rustproofing coating cent concentration wherein the anode is of a metal selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel and lead and maintaining therein a current density of substantially three and a half amperes per square decimeter of cathodic surface whereby there is deposited upon the cathodic surface a magnetite analogue of the anodic metal.
19. The herein described method offorming a double oxide coating upon a ferrous article including the steps of utilizing the ferrous article to be coated as the cathode in a caustic soda solution having a concentration of approximately twenty to twenty-five per cent by weight and three anda half amperes per square decimeter of employing therein a copper anode, and circulating electric current between said elements through the bath at a' current density of approximately three and a half amperes persquare decimeter to effect on the ferrous article simultaneous cathodic deposits of oxide of iron and' oxide of copper.
20. The herein described method of forming a double oxide coating upon a ferrous article including temporarily utilizing the ferrous article to be coated as a cathode element in an alkali electrolytic bath, simultaneously employing thereinan anode element containing copper and passing electric current between the elements through the electrolytic bath at a current density of approximately three and a half amperes per square decimeter of surface to be coated, thereby ef-' fecting upon the surface of the article a cathodic deposit of cupro-magnetite.
21. The herein described method of forming a double oxide coating upon a ferrous article including temporarily utilizing the ferrous article to be coated as a cathode element in an alkali electrolytic bath, simultaneously employing therein an anode element containing chromium and passing electric current between the elements through the electrolytic bath at a current density of approximately three and. a half amperes'per square decimeter of surface to be coated, thereby efiecting upon the surface of the article a cathodic deposit of chromite.
22. The herein described method. 'of surface coating ferrous articles including the steps of submitting the surface to be coated to cathodic and a-half to seven per cent, employing in said bath a copper anode and a ferrous cathode, and
oxidation in the presence of an alkali electrolyte articles a cathodic deposit of a double oxide of iron and the anodic metal.
23. The herein described method of producing an analogueof magnetite including charging an alkali electrolytic bath of approximately twenty to twenty-five per cent concentration with iron.
entering into the solution, employing therein an anodic element selected from a group of metals consisting of copper, chromium, tin, zinc, manganese, nickel, and lead, and a cathodic element of iron .or steel, and circulating through such bath an electric current having a density of approximately three and a' half amperes per square decimeter of cathodic surface whereby there will be deposited upon the cathodic element double oxide of iron and the selected anodic metal.
24. The herein described method of producing an analogue of magnetite including the step of utilizing an alkali electrolytic bath of approximately twenty to twenty-five per cent concentration, circulating an electric current through said bath between iron electrodes until the specific gravity of the solution is increased from two and a half to seven per cent, employing in said-bath an anodic element selected from a group of metals consisting of copper, chormium, tin, zinc, manganese, nickel, and lead, and a cathodic element of iron or steel, and circulating through such bath an electric current having a density of approximately three and a half amperes per square decimeter of cathodic surface whereby there will be deposited upon the cathodic element double oxideof iron and the selected anodic metal.
25. The herein described method of producing copper magnetite including charging an alkali electrolytic bath 'of approximately twenty to twenty-five per cent concentration with iron by v electrolysis between iron electrodes until the speciiic gravity of the bath has been increased two circulating therebetween an electric current having a density of approximately three and a half amperes per square decimeter of cathodic. surface whereby there is deposited upon thecathodic element a double oxide of iron and copper.
26. The method of providing a corrosion resistant coating upon an article which consists in providing a caustic alkali solution, electrolytically introducing iron in solution therein, suspending a ferrous cathode and a non-ferrous anode of a metal selected from a group comprising copper, chromium, tin, zinc, manganese, nickel and lead. and passing an electrical current through the solution between the anode and cathode whereby there is obtained a composite coating upon the cathode of an oxide of iron chemically combined with an oxide of one of the non-ferrous metals used as the anode.
ROBERT H. HARDOEN.
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Application Number | Priority Date | Filing Date | Title |
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US106615A US2275223A (en) | 1936-10-20 | 1936-10-20 | Rustproof material and process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US106615A US2275223A (en) | 1936-10-20 | 1936-10-20 | Rustproof material and process |
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US2275223A true US2275223A (en) | 1942-03-03 |
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US106615A Expired - Lifetime US2275223A (en) | 1936-10-20 | 1936-10-20 | Rustproof material and process |
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Cited By (12)
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US2746915A (en) * | 1951-10-15 | 1956-05-22 | Autoyre Co Inc | Electrolytic metal treatment and article |
US3073763A (en) * | 1958-04-17 | 1963-01-15 | Magneto Chemie N V | Electrolytic production of mixed metal oxides |
US4094750A (en) * | 1977-10-05 | 1978-06-13 | Northrop Corporation | Cathodic deposition of oxide coatings |
US4405573A (en) * | 1981-12-17 | 1983-09-20 | Olin Corporation | Process for preparing potassium ferrate (K2 FeO4) |
US4435256A (en) | 1981-03-23 | 1984-03-06 | Olin Corporation | Process for making potassium ferrate [Fe(VI)] by the electrochemical formation of sodium ferrate |
US4451338A (en) * | 1981-03-23 | 1984-05-29 | Olin Corporation | Process for making a calcium/sodium ferrate adduct by the electrochemical formation of sodium ferrate |
WO2001086029A1 (en) * | 2000-05-06 | 2001-11-15 | Henkel Kommanditgesellschaft Auf Aktien | Electrochemically produced layers for providing corrosion protection or wash primers |
US20060013986A1 (en) * | 2001-10-02 | 2006-01-19 | Dolan Shawn E | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to organic or inorganic coating |
US20090098373A1 (en) * | 2001-10-02 | 2009-04-16 | Henkelstrasse 67 | Anodized coating over aluminum and aluminum alloy coated substrates and coated articles |
US20090258242A1 (en) * | 2001-10-02 | 2009-10-15 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to polytetrafluoroethylene or silicone coating |
US20100000870A1 (en) * | 2001-10-02 | 2010-01-07 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating aluminum and/or titanium with ceramic oxides |
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- 1936-10-20 US US106615A patent/US2275223A/en not_active Expired - Lifetime
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2746915A (en) * | 1951-10-15 | 1956-05-22 | Autoyre Co Inc | Electrolytic metal treatment and article |
US3073763A (en) * | 1958-04-17 | 1963-01-15 | Magneto Chemie N V | Electrolytic production of mixed metal oxides |
US4094750A (en) * | 1977-10-05 | 1978-06-13 | Northrop Corporation | Cathodic deposition of oxide coatings |
US4435256A (en) | 1981-03-23 | 1984-03-06 | Olin Corporation | Process for making potassium ferrate [Fe(VI)] by the electrochemical formation of sodium ferrate |
US4451338A (en) * | 1981-03-23 | 1984-05-29 | Olin Corporation | Process for making a calcium/sodium ferrate adduct by the electrochemical formation of sodium ferrate |
US4405573A (en) * | 1981-12-17 | 1983-09-20 | Olin Corporation | Process for preparing potassium ferrate (K2 FeO4) |
US20070144914A1 (en) * | 2000-05-06 | 2007-06-28 | Mattias Schweinsberg | Electrochemically Produced Layers for Corrosion Protection or as a Primer |
WO2001086029A1 (en) * | 2000-05-06 | 2001-11-15 | Henkel Kommanditgesellschaft Auf Aktien | Electrochemically produced layers for providing corrosion protection or wash primers |
US20040099535A1 (en) * | 2000-05-06 | 2004-05-27 | Mattias Schweinsberg | Electrochemically produced layers for providing corrosion protection or wash primers |
US20060013986A1 (en) * | 2001-10-02 | 2006-01-19 | Dolan Shawn E | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to organic or inorganic coating |
US20090098373A1 (en) * | 2001-10-02 | 2009-04-16 | Henkelstrasse 67 | Anodized coating over aluminum and aluminum alloy coated substrates and coated articles |
US20090258242A1 (en) * | 2001-10-02 | 2009-10-15 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to polytetrafluoroethylene or silicone coating |
US20100000870A1 (en) * | 2001-10-02 | 2010-01-07 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating aluminum and/or titanium with ceramic oxides |
US7820300B2 (en) | 2001-10-02 | 2010-10-26 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to organic or inorganic coating |
US8361630B2 (en) | 2001-10-02 | 2013-01-29 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating an aluminum substrate with ceramic oxides prior to polytetrafluoroethylene or silicone coating |
US8663807B2 (en) | 2001-10-02 | 2014-03-04 | Henkel Ag & Co. Kgaa | Article of manufacture and process for anodically coating aluminum and/or titanium with ceramic oxides |
US9023481B2 (en) | 2001-10-02 | 2015-05-05 | Henkel Ag & Co. Kgaa | Anodized coating over aluminum and aluminum alloy coated substrates and coated articles |
US9701177B2 (en) | 2009-04-02 | 2017-07-11 | Henkel Ag & Co. Kgaa | Ceramic coated automotive heat exchanger components |
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