US1787672A - Method of treating thorium - Google Patents
Method of treating thorium Download PDFInfo
- Publication number
- US1787672A US1787672A US282895A US28289528A US1787672A US 1787672 A US1787672 A US 1787672A US 282895 A US282895 A US 282895A US 28289528 A US28289528 A US 28289528A US 1787672 A US1787672 A US 1787672A
- Authority
- US
- United States
- Prior art keywords
- thorium
- metal
- treating
- metals
- atmospheric
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- ZSLUVFAKFWKJRC-IGMARMGPSA-N 232Th Chemical compound [232Th] ZSLUVFAKFWKJRC-IGMARMGPSA-N 0.000 title description 15
- 229910052776 Thorium Inorganic materials 0.000 title description 15
- 238000000034 method Methods 0.000 title description 14
- 229910052751 metal Inorganic materials 0.000 description 34
- 239000002184 metal Substances 0.000 description 34
- 150000002739 metals Chemical class 0.000 description 15
- 239000007789 gas Substances 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 9
- 238000005260 corrosion Methods 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 229910052684 Cerium Inorganic materials 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 229910052770 Uranium Inorganic materials 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- 229960000583 acetic acid Drugs 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 3
- 239000012362 glacial acetic acid Substances 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000009877 rendering Methods 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- DNYWZCXLKNTFFI-UHFFFAOYSA-N uranium Chemical compound [U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U][U] DNYWZCXLKNTFFI-UHFFFAOYSA-N 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000010301 surface-oxidation reaction Methods 0.000 description 2
- 238000005494 tarnishing Methods 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- GPFIZJURHXINSQ-UHFFFAOYSA-N acetic acid;nitric acid Chemical compound CC(O)=O.O[N+]([O-])=O GPFIZJURHXINSQ-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- -1 enamels Substances 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000006557 surface reaction Methods 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
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/28—Anodisation of actinides or alloys based thereon
Definitions
- This invention relatesto the art of metallurgy and more particularly relates .to the art of rendering metals resistant to atmospheric corrosion, and comprises essentially in an electrolytic method of treating the surfaces of highly'reactive and easily oxidizable metals such as thorium, cerium, zirconium, titanium, uranium, etc., whereby the metal body is rendered substantially. resistant to surface corrosion when exposed to atmospheric conditions.
- the formed and fabricated metal bodies are found to. be highlyreactive towards atmospheric gases, progressively combining with oxygen, nitrogenand hydrogen at the exposed surface to: form amorphous films of oxide, nitride and hydride. .This re action continues indefinitely-"and will cause eventually'entir'e destruction'of the' metal body.
- the surface oxidation only proceeds to the extent necessary to form-anadherentprotective film thereon which is impenetrable to atmospheric gases.
- Other metals such as iron form surface oxides which are penetrable to atmospheric gases and corrosion proceeds indefinitelyv.
- the present invention is directed to a method whereby the highly reactive metals mentioned above may be rendered substantially passive or non-reactive towards atmospheric gases.
- Another object is to produce the highly reactive metals thorium, uranium, cerium, zirconium, titanium, etc., in a form substantially resistant to atmospheric corrosion.
- my invention contemplates imparting to the surface of these highly reactive metals a closely adherent, gasimpervious film of what I consider to be an oxide compound of the particular metal.
- the means I employ in forming this film is electrolytic, thatis, I make the metal the anode in an electrolytic bath and subject it to such a current density as to cause the-formation upon the surface of what I believe to be an oxide compound of the metal.
- This film in addition to being impervious to gas penetration at room temperatures is, moreover, sufiiciently transparent so that the clean metallic surface underneath is fully visible.
- the electrolytic bath'I prefer to employ is comprised mainly of glacial acetic acid containing as an ionizable constituent concentrated nitric acid, in varyingproportions depending upon the metal being treated, current density used, etc.
- Formed articles such as stamped or rolled sheets, wire rods, etc., which are highly compacted, resist the disintegrating eflect of atmospheric gases longer than unworked articles, such as heat treated or semi-sintered ingots having approximately 70 to 80 er cent the denslty o the worked articles. he rate of penetration also depends upon the kind of atmospheric gases present.
- the thorium article to be treated is made the anode in an electrolytic article being bath of the type described, and suflicient D. C. voltage impressed across the terminals to free the current therethrough.
- a variable resistance should be included within the circuit so that the current (amperes) may be controlled Within the rather wide limits required in treating articles of variable size and surface areas.
- the current density which I have found to be most efficient in treating thorium rods is approximately 0.25-0.50 amperes per square inch. This, however, may vary within rather wide limits, depending upon the particular treated i. e., rod, wire, bar, or relatively small piece, such as an X-ray target prior to mounting on a backing or small electrodes utilized in the construction of gas rectifiers.
- the time interval is a variable factor depending upon the size and'length of the particular thorium article being treated.
- the rogress of the treatment inay be followe by the development of dark grey or black deposit upon the surface of the msae'ra thorium.
- This black or dark grey deposit may be rinsed ofi in pure ethyl alcohol or other solvent inert with respect to the thorium or other reactive metal used, after which the deposit may be easil rubbed off exposing beneath a clean, metal ic surface.
- the process of rendering thorium reto render the metal resistant to atmospheric corrosion which comprises anodically treating the metal in an electrolytic bath comprised of the latter up to approximately 30 percent b volume of the former.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Description
36o Drawing.
[TED SITES ATENT OFFICE EDMUND S. DAVENPORT, OF BLOOMFIELD, NEW JERSEY, ASSIGNOB. 'I'O WESTINGHOUSE LP COMPANY, A CORPORATION OF PENNSYLVANIA mnrnon or TREATING momma This invention relatesto the art of metallurgy and more particularly relates .to the art of rendering metals resistant to atmospheric corrosion, and comprises essentially in an electrolytic method of treating the surfaces of highly'reactive and easily oxidizable metals such as thorium, cerium, zirconium, titanium, uranium, etc., whereby the metal body is rendered substantially. resistant to surface corrosion when exposed to atmospheric conditions.
Heretofore many methods have been devised wherein. the processes of atmospheric corrosion or oxidation on exposed metal surfaces have either been arrested or prevented. The surfaces have been coated with various paints, enamels, lacquers, non-corrosive metal s, etc. With some metals one process is applicable and withother metals another process is applicable.
In the manufacture of coherent metal bodies of highly reactive metals, such as thorium, uranium, zirconium, cerium, titanium, etc., the formed and fabricated metal bodies are found to. be highlyreactive towards atmospheric gases, progressively combining with oxygen, nitrogenand hydrogen at the exposed surface to: form amorphous films of oxide, nitride and hydride. .This re action continues indefinitely-"and will cause eventually'entir'e destruction'of the' metal body.
' In some metals, such as aluminum, magnesium, chromium, nickel, etc., the surface oxidation only proceeds to the extent necessary to form-anadherentprotective film thereon which is impenetrable to atmospheric gases. Other metals such as iron form surface oxides which are penetrable to atmospheric gases and corrosion proceeds indefinitelyv.
In the latter class of metals some or these may be so treated chemically as to form on the surface an imparted oxide structure which is of a higher or lower state of chemical oxidation not normal .to the metal, but which is impenetrable to atmospheric gases. Such a Application filed June 4, 1828. Serial No. 282,885.
ways and many other metals may be chemically treated so as to arrest or inhibit surface reaction with atmospheric gases.
The present invention is directed to a method whereby the highly reactive metals mentioned above may be rendered substantially passive or non-reactive towards atmospheric gases.
Another object is to produce the highly reactive metals thorium, uranium, cerium, zirconium, titanium, etc., in a form substantially resistant to atmospheric corrosion.
Other objects and advantages will beapparent as the invention is more fully disclosed.
Broadly considered, my invention contemplates imparting to the surface of these highly reactive metals a closely adherent, gasimpervious film of what I consider to be an oxide compound of the particular metal.
' The means I employ in forming this film is electrolytic, thatis, I make the metal the anode in an electrolytic bath and subject it to such a current density as to cause the-formation upon the surface of what I believe to be an oxide compound of the metal. This film in addition to being impervious to gas penetration at room temperatures is, moreover, sufiiciently transparent so that the clean metallic surface underneath is fully visible.
The electrolytic bath'I prefer to employ is comprised mainly of glacial acetic acid containing as an ionizable constituent concentrated nitric acid, in varyingproportions depending upon the metal being treated, current density used, etc.
Other solutions and combinations of electrolytic baths may beemployed in the practice of my invention which will produce essentially the same result as the one described,
that is the release at the anode of oxygen in such a manner as to form this closely adherent oxidized film upon the surface of the metal body.
The main reason why I prefer to use the acetic acid-nitric acid combination is that this solution may be prepared initially substantially. anhydrous, which appears to be a desirable feature in handling such highly reactive metals as contemplated in this disclosure.
The highly reactive metals mentioned, moreover, will require in some instances'some alteration in the chemical components of the bath as mentioned or in the particular current densities applied to produce the result desired, but as a specific embodiment of the nature of my invention I will describe the process I employ in treating thorium so as. to render it substantially impervious to atmospheric corrosion.
It is a well known fact that a freshly olished or exposed surface of thorium Will become rapidly tarnished and darkened on exposure to the atmosphere for a few hours or days. The tarnishing or darkening proceeds from day to day, and depending upon the particular metal under observation will proceed indefinitely.
Formed articles, such as stamped or rolled sheets, wire rods, etc., which are highly compacted, resist the disintegrating eflect of atmospheric gases longer than unworked articles, such as heat treated or semi-sintered ingots having approximately 70 to 80 er cent the denslty o the worked articles. he rate of penetration also depends upon the kind of atmospheric gases present.
In my process the thorium article to be treated is made the anode in an electrolytic article being bath of the type described, and suflicient D. C. voltage impressed across the terminals to free the current therethrough. A variable resistance should be included within the circuit so that the current (amperes) may be controlled Within the rather wide limits required in treating articles of variable size and surface areas.
The current density which I have found to be most efficient in treating thorium rods is approximately 0.25-0.50 amperes per square inch. This, however, may vary within rather wide limits, depending upon the particular treated i. e., rod, wire, bar, or relatively small piece, such as an X-ray target prior to mounting on a backing or small electrodes utilized in the construction of gas rectifiers.
The time interval is a variable factor depending upon the size and'length of the particular thorium article being treated. I
ave determined that with rods of approximately mils. diameter (.080 inches) and approximately 2 inches immersed length, the approximate minimum time interval at the current density mentioned is 2 to 3 minutes. It shouldbe appreciated that the problem is not so much a question of minimum or maximum time interval employed except in so far as the operation of-the invention on a production basis is concerned.
The rogress of the treatment inay be followe by the development of dark grey or black deposit upon the surface of the msae'ra thorium. This black or dark grey deposit may be rinsed ofi in pure ethyl alcohol or other solvent inert with respect to the thorium or other reactive metal used, after which the deposit may be easil rubbed off exposing beneath a clean, metal ic surface.
When properly treated this surface will remain bright and untarnished for prolonged periods of time, and such articles have been found to be increasingly useful in the arts, especially in radio and X-ray appliances where heretofore it has been diflicult to apply the same, due to the surface oxidation and combination with deleterious impurities. q
I have found it advisable in the practice of my invention to properly space the electrodes in the electrolytic bath or to so insulate the anode from the cathode that the full oxidizing effect at the anode may be employed without being deleteriously effected by the hydrogen liberated at the cathode and in treating drawn or swaged thorium wire by my process I may do so in a continuous manner if desired. In treating rods, bars, or small isolated pieces, such as X-ray tar-' gets, etc., provision should be made to continuously rotate the bar or rod during the treating process so as to distribute the anode oxidizing effect.
By the practice of my invention I am able to producea substantially non-oxidizing, non-tarnishing body of the highly-reactive metal thorium which may be utilized in ,the arts. By the practice of my invention I also am able to so treat the surface of other I metals so that they substantially withstand 1 atmospheric corrosion.
There may be many other methods of obtaining the same result and other solution combinations than the one specifically mentioned may be employed in the electrolytic bath, but all such variations and combinations are anticipated as may fall within the following claims.
What is claimed is:
1. The process of rendering thorium msistent to atmospheric corrosion which comprises anodically treating the metal in an electrolytic bath comprised of glacial acetic acid containing a proportion of an ionizable the anode.
2. The process of rendering thorium reto render the metal resistant to atmospheric corrosion which comprises anodically treating the metal in an electrolytic bath comprised of the latter up to approximately 30 percent b volume of the former.
glacial acetic acid and nitric acid, a component bemg present in amounts 1 1'15 constituent capable of yielding oxygen at
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US282895A US1787672A (en) | 1928-06-04 | 1928-06-04 | Method of treating thorium |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US282895A US1787672A (en) | 1928-06-04 | 1928-06-04 | Method of treating thorium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1787672A true US1787672A (en) | 1931-01-06 |
Family
ID=23083582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US282895A Expired - Lifetime US1787672A (en) | 1928-06-04 | 1928-06-04 | Method of treating thorium |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1787672A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2442591A (en) * | 1942-09-30 | 1948-06-01 | American Rolling Mill Co | Electrolytic polishing of stainless steel |
| US2516105A (en) * | 1945-06-20 | 1950-07-25 | Mateosian Edward Der | Electrolytic polishing of metals |
| US2794932A (en) * | 1951-01-12 | 1957-06-04 | Ets Claude Paz & Silva | Gas absorbent material |
| US2836548A (en) * | 1944-10-25 | 1958-05-27 | Allen G Gray | Surface treatment of metallic uranium |
| US2872387A (en) * | 1948-05-12 | 1959-02-03 | Kolodney Morris | Anodic treatment of uranium |
| US2884364A (en) * | 1946-05-14 | 1959-04-28 | Elmer W Rebol | Method of electroplating on uranium |
| US2894883A (en) * | 1949-07-18 | 1959-07-14 | David E Walker | Method of electropolishing uranium |
| US2987454A (en) * | 1957-11-27 | 1961-06-06 | Kopelman Bernard | Electrolytic process for producing metals |
| US3002899A (en) * | 1959-07-31 | 1961-10-03 | Jr Walter E Reid | Adhesion of nickel to chromium |
| US3102086A (en) * | 1957-07-26 | 1963-08-27 | Ici Ltd | Method of improving the corrosion resistance of titanium metals |
| US5264109A (en) * | 1991-09-16 | 1993-11-23 | Siemens Power Corporation | Zirconium and zirconium alloy passivation process |
-
1928
- 1928-06-04 US US282895A patent/US1787672A/en not_active Expired - Lifetime
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2442591A (en) * | 1942-09-30 | 1948-06-01 | American Rolling Mill Co | Electrolytic polishing of stainless steel |
| US2836548A (en) * | 1944-10-25 | 1958-05-27 | Allen G Gray | Surface treatment of metallic uranium |
| US2516105A (en) * | 1945-06-20 | 1950-07-25 | Mateosian Edward Der | Electrolytic polishing of metals |
| US2884364A (en) * | 1946-05-14 | 1959-04-28 | Elmer W Rebol | Method of electroplating on uranium |
| US2872387A (en) * | 1948-05-12 | 1959-02-03 | Kolodney Morris | Anodic treatment of uranium |
| US2894883A (en) * | 1949-07-18 | 1959-07-14 | David E Walker | Method of electropolishing uranium |
| US2794932A (en) * | 1951-01-12 | 1957-06-04 | Ets Claude Paz & Silva | Gas absorbent material |
| US3102086A (en) * | 1957-07-26 | 1963-08-27 | Ici Ltd | Method of improving the corrosion resistance of titanium metals |
| US2987454A (en) * | 1957-11-27 | 1961-06-06 | Kopelman Bernard | Electrolytic process for producing metals |
| US3002899A (en) * | 1959-07-31 | 1961-10-03 | Jr Walter E Reid | Adhesion of nickel to chromium |
| US5264109A (en) * | 1991-09-16 | 1993-11-23 | Siemens Power Corporation | Zirconium and zirconium alloy passivation process |
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