US1224339A - Vapor treatment of metals. - Google Patents
Vapor treatment of metals. Download PDFInfo
- Publication number
- US1224339A US1224339A US82966214A US1914829662A US1224339A US 1224339 A US1224339 A US 1224339A US 82966214 A US82966214 A US 82966214A US 1914829662 A US1914829662 A US 1914829662A US 1224339 A US1224339 A US 1224339A
- Authority
- US
- United States
- Prior art keywords
- vapor
- metal
- iron
- temperature
- pressure
- 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
- 229910052751 metal Inorganic materials 0.000 title description 36
- 239000002184 metal Substances 0.000 title description 36
- 150000002739 metals Chemical class 0.000 title description 7
- 238000011282 treatment Methods 0.000 title description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 42
- 239000007789 gas Substances 0.000 description 22
- 229910052742 iron Inorganic materials 0.000 description 21
- 238000000034 method Methods 0.000 description 20
- 239000000463 material Substances 0.000 description 19
- 230000008569 process Effects 0.000 description 18
- 239000000126 substance Substances 0.000 description 9
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- 239000007787 solid Substances 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000011358 absorbing material Substances 0.000 description 2
- 229910052787 antimony Inorganic materials 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 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 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000005246 galvanizing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C23C16/00—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
- C23C16/06—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material
- C23C16/18—Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the deposition of metallic material from metallo-organic compounds
Definitions
- Our invention therefore comprises a method of forming a surface compound or alloy which possesses the desired properties.
- iron so that the outer layer w1ll be rust proof; we may treat copper or iron, etc., so that its outer layer will be extremely hard or extremely tough, or resist certain agents, etc. i
- a further fact which is well established is that the presence of free ions has a marked efiect in producing a condensation of a vapor or suspended matter in a gas.
- the result is a rust proof metal having all of the qualities of a very high grade steel or iron, but much more permanent than galvanizing or similar treatments.
- the process which we have devised is not necessarily dependent upon having the substances supplying the vapor in the form of a powder, as in the example illustrated, although a substance in this form may often be raised to a temperature above the melting point without fusing the articles together.
- the elevated temperature which can thus be secured is of material assistance in securing a rich vapor which naturally hastens the process and therefore is an advantage in many cases.
- a further advantage of using the material supplying the vapor in the powdered form is the enormously increased surface which can thus be Secured, thus giving a richer vapor, since If now, in addition to raisthe amount of material vaporized at a given temperature and pressure increases with increased evaporating surface. ticularly of value when the boiling point of the vapor giving material is above the temperature. at which the deposition occurs.
- the surface combination may be effected without the contact in the solid form of the treating material with the surface to be treated.
- a portion of zinc dust may be placed in, one part of the vacuum chamber, the iron to be treated in another portion of the chamber and the reaction will proceed on sufliciently reducing the pressure and applying the necessary heat, although of course the zinc and iron are in substantial contact.
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Vapour Deposition (AREA)
- Physical Vapour Deposition (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
WILLIAM A. DARRAH AND SAMUEL TROOD, OF WILKINSBTTRG, PENNSYLVANIA, ASSIGNORS TO INDUSTRIAL DEVELOPMENT COMPANY, A CORPORATION OF VAPOR TREATMENT OF METALS.
To all whom it may concern:
Be it known that We, WILLIAM A. DAnnAi-r and SAMUEL Tnooo, citizens of the United to change the qualities of a metal by the addition of other metals or other substances,
' and it may be expedient for reasons of cost, or otherwise to effect this addition after the metal is brought into the final form; in other words, under conditions such that a surface alloy or compound is preferable to a homogeneous metal. Our invention, therefore comprises a method of forming a surface compound or alloy which possesses the desired properties. Thus we may treat iron so that the outer layer w1ll be rust proof; we may treat copper or iron, etc., so that its outer layer will be extremely hard or extremely tough, or resist certain agents, etc. i
The depth to which this process is applicable, is of course dependent upon the surrounding conditions, as will be later explained.
It is a well known fact that all common metals are extremely porous. This is visible with the magnifying glass as well as readily demonstrated by certain physical experiments. Thus, if an iron wire be placed in an exhaust tube, and then heated to incandescence, as for instance, by passing a current through the wire, the pressure within the tube rises materially, and gas is evolved for a very considerable time, indicating that iron (and practically all other metals), contain large volumes of gases. The condition of the metal may be graphically described as resembling a sponge soaked with water.
There also appears to be an electrical c0n-- dition accompanying the evolution of gases from a metal, inasmuch as we have found that the evolved gases usually contain a number of free ions. This is particularly the case if the temperature of the metal is high at the time the gases are given out.
Patented May 1, 1917.
PENNSYLVANIA.
.1,224 ,339 Specification of Letters Patent.
No Drawing.
Application filed April 4, 1914. Serial No. 829,662.
Naturally the exposed surface of a metal, is the only portion which activcly takes part in evolving or absorbing gases, so that the larger the area of the surface exposed, the greater the evolution of gas, other conditions being equal.
Now it is a well known fact that all materials have a definite vapor pressure, depending mainly on the nature of the material, the nature of the surrounding matorials, the temperature and the pressure. It therefore follows, that under all conditions, all substances are surrounded by a certain amount of their own vapor. The vapor can be increased in amount by increasing the temperature and decreasing the pressure. This is well illustrated by the so called triple point condition of a substance at which point the material can exist simultaneously as a solid liquid and gas. On lowering the pressure, it is possible in many cases to cause a solid to pass directly from a solid to a gas.
A further fact which is well established is that the presence of free ions has a marked efiect in producing a condensation of a vapor or suspended matter in a gas.
It follows, therefore, that if a metal be heated in the presence of a vapor under such conditions that the gases or vapors contained within the metal are in part liberated, then as these liberated gases or vapors contain some free ions, they will cause the precipitation within the pores of the metal and on the surface layer of a portion of the external vapor in which the metal is heated.
It must be understood of course, that while the above theory explains the reactions which we are able to produce, yet we are not certain of its accuracy. Furthermore, since this invention comprises a process of treating metals, we do not'desire to be confined to any particular theory, but only to the process which we have devised.
The process as well as the theory described above, may be well illustratedby the specific case of the treatment of iron with aluminum, which is used only as an example. If a piece of iron is placed in a closed air tight vessel, powdered metallic aluminum, and the temperature raised to even 1000 C. no material surrounded by change can be noted in the iron, and the amount of aluminum thus absorbed in a few hours is so small as to be negligible as far as any effect upon the properties of the iron is concerned. ing the temperature, the pressure within the vessel is reduced by removing the air an appreciable amount of aluminum will pass into the surface layer of the iron. Under these conditions, a very appreciable effect can be produced if the temperature does not exceed 7 00 C. and the vacuum is suliicient to support 20 inches of mercury. These conditions are of course to be considered as merely examples, as copper, brass, platinum, and many other metals may be substituted for the iron and sodium, calcium, zinc, etc., may be substituted for the aluminum or even such substances may beused as sulfur, arsenic, antimony, phosphorus, silicon, carbon, boron and some of their compounds.
In the case of the aluminum treated iron, the result is a rust proof metal having all of the qualities of a very high grade steel or iron, but much more permanent than galvanizing or similar treatments.
In view of the above facts, it appears that when a metal is heated in the presence of the vapor of another metal, or the vapor of. other elements or compounds, the metal evolves a portion of the gases or vapor which it contains, and in exchange condenses some of the other vapors within its pores.
Iron heated with powdered antimony to a temperature below the melting point of the latter for several hours at a reduced pressure, gives an excellent rust resisting surface layer. A vacuum of twenty-six inches of mercury gives very good results in this case, although it is not necessary to reduce the pressure as much as this. As will be evident, however, a reduced pressure will hasten the process with a given temperature, or if the same time is allowed, a reduced pressure Will allow a reduction in temperature.
The process which we have devised is not necessarily dependent upon having the substances supplying the vapor in the form of a powder, as in the example illustrated, although a substance in this form may often be raised to a temperature above the melting point without fusing the articles together. The elevated temperature which can thus be secured is of material assistance in securing a rich vapor which naturally hastens the process and therefore is an advantage in many cases. A further advantage of using the material supplying the vapor in the powdered form is the enormously increased surface which can thus be Secured, thus giving a richer vapor, since If now, in addition to raisthe amount of material vaporized at a given temperature and pressure increases with increased evaporating surface. ticularly of value when the boiling point of the vapor giving material is above the temperature. at which the deposition occurs.
The temperatures Which we have found effective in the case of depositingaluminum vapor in iron is a full-red heat. We do not desire to be limited to this temperature, however, as each material used to supply the vapor, as well as each material absorbing the vapor, and each combination of vapor giving material with vapor absorbing material may require a different temperature for securing most satisfactory results.
A further point Which should be noted is that the evolution of gas from the absorbing substance appears to function in the absorption, so that by the medium of evolved gas, it is possible to cause the condensation of one substance within the pores or surface layer of another at a temperature which is actually below the melting point of the material deposited. We have also found that the evolved gas need not beheld in the metal purely by physical combination, as gases which are liberated by a chemical action such as a decomposition reduction of an oxid, or formation of a compound, are also effective. The process which we employ may thus be made more efiective in some cases by putting the vapor absorbing material in a condition such that when raised to the proper temperature and proper pressure, a considerable amount of gas or vapor will be evolved. One method of causing this is to make the material the pole of an elec- This is partrolytic cell at which hydrogen is evolved.
Under these conditions, sufficient gas will be absorbed by the metal to assist in the subsequent vapor treatment.
From the above description, it will be evident that our process comprises essentially the heating of metal to be treated in the presence of the vapor to beabsorbed for a given time and at a reduced pressure. The exact value of temperature, pressure and. time depend of course upon the materials used and other conditions as set forth.
Actual experience with the described has developed the fact that the surface combination may be effected without the contact in the solid form of the treating material with the surface to be treated. Thus a portion of zinc dust may be placed in, one part of the vacuum chamber, the iron to be treated in another portion of the chamber and the reaction will proceed on sufliciently reducing the pressure and applying the necessary heat, although of course the zinc and iron are in substantial contact.
process here Having described our invention what we claim as new and desire to secure by Letters Patent is 1.. The process of forming a compound in a metal by heating the metal under reduced pressure in the presence of the vapor of the compound formlng material.
2. The process of forming an alloy of a metal by heating the metal under reduced pressure in the presence of the vapor of the alloy forming metal.
3. The process of forming an iron alloy by heating the iron under reduced pressure in the presence of the vapor of the alloy forming material.
4. The process of condensing a vapor within a metal by surrounding the metal while heated, by the desired vapor at a pressure below atmospheric pressure.
5. The process of forming a coating of zinc upon iron by heating the said iron in the presence of zinc vapor under reduced pressure in a chamber from which other gases and vapors have been substantially exhausted.
6. The process of depositing zinc on iron by heating the iron and zinc dust together removing all vapors and under reduced pressure in a chamber from which other vapors than zinc have been substantially exhausted.
7. The process of condensing a vapor within a metal by heating the metal in the presence of the desired vapor in a chamber from which other gases and vapors have been substantially exhausted, the pressure within said chamber being maintained lower than atmospheric.
8. The process of condensing a vapor upon a metal which consists in placing said metal in a chamber in the presence of the material to supply the desired vapor, substantially gases but those due to the treating material and heating said chamber while the contents are maintained at a pressure lower than atmospheric.
In testimony whereof, we have hereunto subscribed our names this third day of April 1914.
WILLIAM A. DARRAI-I. SAMUEL TROOD.
Witnesses:
A. QH MYTHoFF, D. A. BARBOR.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82966214A US1224339A (en) | 1914-04-04 | 1914-04-04 | Vapor treatment of metals. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US82966214A US1224339A (en) | 1914-04-04 | 1914-04-04 | Vapor treatment of metals. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1224339A true US1224339A (en) | 1917-05-01 |
Family
ID=3292193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US82966214A Expired - Lifetime US1224339A (en) | 1914-04-04 | 1914-04-04 | Vapor treatment of metals. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1224339A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2877143A (en) * | 1956-11-20 | 1959-03-10 | Rca Corp | Method of treating glass |
| US3127283A (en) * | 1964-03-31 | Microns for | ||
| US4680908A (en) * | 1980-04-14 | 1987-07-21 | Amoco Corporation | Refractory anchor |
-
1914
- 1914-04-04 US US82966214A patent/US1224339A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3127283A (en) * | 1964-03-31 | Microns for | ||
| US2877143A (en) * | 1956-11-20 | 1959-03-10 | Rca Corp | Method of treating glass |
| US4680908A (en) * | 1980-04-14 | 1987-07-21 | Amoco Corporation | Refractory anchor |
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