US3847685A - Oxide coated metal discs and method of making the same - Google Patents
Oxide coated metal discs and method of making the same Download PDFInfo
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- US3847685A US3847685A US00010533A US1053370A US3847685A US 3847685 A US3847685 A US 3847685A US 00010533 A US00010533 A US 00010533A US 1053370 A US1053370 A US 1053370A US 3847685 A US3847685 A US 3847685A
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- 229910052751 metal Inorganic materials 0.000 title claims description 27
- 239000002184 metal Substances 0.000 title claims description 21
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000007769 metal material Substances 0.000 claims abstract description 36
- 238000000576 coating method Methods 0.000 claims abstract description 23
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 13
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 13
- 230000001590 oxidative effect Effects 0.000 claims abstract description 12
- 230000001464 adherent effect Effects 0.000 claims abstract description 8
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 8
- 239000000463 material Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 29
- 229910045601 alloy Inorganic materials 0.000 claims description 19
- 239000000956 alloy Substances 0.000 claims description 19
- 239000011248 coating agent Substances 0.000 claims description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 14
- 239000002344 surface layer Substances 0.000 claims description 12
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 10
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 10
- 150000002739 metals Chemical class 0.000 claims description 7
- 229910001963 alkali metal nitrate Inorganic materials 0.000 claims description 5
- 238000007654 immersion Methods 0.000 claims description 5
- 239000011780 sodium chloride Substances 0.000 claims description 5
- 235000010344 sodium nitrate Nutrition 0.000 claims description 5
- 239000004317 sodium nitrate Substances 0.000 claims description 5
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 4
- 239000010410 layer Substances 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 abstract description 8
- 239000010935 stainless steel Substances 0.000 abstract description 7
- 238000005299 abrasion Methods 0.000 abstract description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000010276 construction Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- WMFOQBRAJBCJND-UHFFFAOYSA-M lithium hydroxide Inorganic materials [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-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
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
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
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/70—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using melts
- C23C22/72—Treatment of iron or alloys based thereon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/923—Physical dimension
- Y10S428/924—Composite
- Y10S428/926—Thickness of individual layer specified
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/922—Static electricity metal bleed-off metallic stock
- Y10S428/9265—Special properties
- Y10S428/929—Electrical contact feature
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/1241—Nonplanar uniform thickness or nonlinear uniform diameter [e.g., L-shape]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/125—Deflectable by temperature change [e.g., thermostat element]
- Y10T428/12521—Both components Fe-based with more than 10% Ni
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12535—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.] with additional, spatially distinct nonmetal component
- Y10T428/12611—Oxide-containing component
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12493—Composite; i.e., plural, adjacent, spatially distinct metal components [e.g., layers, joint, etc.]
- Y10T428/12771—Transition metal-base component
- Y10T428/12861—Group VIII or IB metal-base component
- Y10T428/12951—Fe-base component
- Y10T428/12958—Next to Fe-base component
- Y10T428/12965—Both containing 0.01-1.7% carbon [i.e., steel]
Definitions
- pressure sensitive metal diaphragms incorporated in pressure switches are deformed to provide the diaphragms with a dished configuration such that the diaphragms are adapted to retain their original dished configuration under the force of selected applied fluid pressures but are adapted to move with snap-action to inverted dished configurations in response to selected greater applied fluid pressures.
- bimetallic thermostatic metal discs are frequently provided with deformed portions such that the discs have selected dished configurations under one set of temperature conditions but are adapted to move with snap-action to inverted dished configurations under other temperature conditions.
- FIG. 3 is a section view along a transverse axis of a diaphragm made in accordance with this invention.
- the first process bath 16 comprises an oxidizing bath of fused alkali metal hydroxide materials which can include fused lithium, sodium or potassium hydroxide and the like alone or in combination with each other and which can also include additions of fused alkali metal nitrate and chloride salts.
- the bath 16 has a composition, by weight, from about 7 to 32 percent sodium nitrate, from about 1 to 20 percent sodium chloride, and the balance sodium hydroxide, the preferred bath embodying approximately percent hydroxide, 20 percent sodium nitrate and 10 percent sodium chloride by weight.
- the strip material 10 comprises any of the various commercially available stainless steels, including 300 Series and 400 Series Stainless Steel such-as Type 302 Stainless Steel having a nominal composition, by weight, of 18 percent chromium, 8 percent nickel and the balance iron, and where the bath l6 embodies 70 percent sodium hydroxide, 20 percent sodium nitrate, and 10 percent sodium chloride
- the bath temperature and speed of movement of the strip 10 is preferably maintained at values falling on or between curves A and B in FIG. 4, the bath temperature and strip speed preferably being controlled in the manner indicated by curve C. That is,
- the metal strip material 10 should be free of any oxide scale or the like but need not be processed in any particular manner prior to immersion in the bath 16. However, it is desirable for achieving product uniformity to clean gross contaminants such as oils and greases from the strip prior to bath immersion. Such gross contaminants will be removed from the strip by immersion of the strip in the bath but for product uniformity it is desirable that all portions of the strip surface be exposed to the bath for the same period of time.
- said oxidizing bath comprises fused materials selected from the group consisting of alkali metal hydroxides, alkali metal nitrates and alkali metal chlorides.
- said oxidizing bath comprises, by weight, from 7 to 32 percent alkali metal nitrate, from 1 to 20 percent alkali metal chloride and the balance alkali metal hydroxide.
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- 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)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Metal materials and elements such as stainless steel diaphragms and the like are immersed in oxidizing, fused, alkali metal hydroxide baths to provide the metal materials with adherent metal oxide coatings to protect the metal materials from abrasion.
Description
United States Patent [1 1 Baboian et al.
[ OXIDE COATED METAL DISCS AND METHOD OF MAKING THE SAME [75] lnventors: Robert Baboian, North Attleboro,
Mass.; Peter O. Fiore, Cumberland,
[73] Assignee: Texas Instruments Incorporated,
Dallas, Tex.
[22] Filed: Feb. 11, 1970 21 Appl. No.: 10,533
[52] US. Cl. 148/315, 29/l9l.6, 29/195 M, 29/195.5, 143/611, 337/53, 337/89, 337/379 [51] Int. Cl. C231 7/02 [58] Field of Search 148/611, 31.5; 117/128, 117/130 R, 223; 29/l95.5, 196, 195, 191.6;
[56] References Cited UNITED STATES PATENTS 2,585,704 2/1952 Vaughan et al 337/379 X 1 Nov. 12, 1974 2,750,301 6/1956 Wenderott 148/611 X 1,879,701 9/1932 Marino 148/6.11 1,895,590 l/l933 Spencer 29/195.5 1,247,086 12/1917 Crowe 148/611 2,479,979 8/1949 Spence et a1. 148/6.11 X
Primary ExaminerCharles E. Van Horn Assistant ExaminerCaleb Weston Attorney, Agent, or Firm-Harold Levine; John A. Haug; James P. McAndrews [5 7 ABSTRACT Metal materials and elements such as stainless steel diaphragms and the like are immersed in oxidizing, fused, alkali metal hydroxide baths to provide the metal materials with adherent metal oxide coatings to protect the metal materials from abrasion.
9 Claims, 4 Drawing Figures iii??? In ventons will II'IIIIIIIIIIIII PATENTEDNDV 12 mm wl 3% BF t m fir P W PATENTEDHUY 12 m4 31847385 sum 2 or 2 TEMPERATURE Inventors: Robert .Bhboian Peter 0.1 1102%, J yaw/w OflZQW.
Aug
OXIDE COATED METAL DISCS AND METHOD OF MAKING THE SAME In many commercially available pressure switches, thermostats and the like, metal diaphragms, thermostatic metal elements and the like are used to sense environmental conditions such as pressures and temperatures. In such devices, these metal elements are frequently formed in such a way that precisely controlled stress conditions are established in the metal materials of the elements, whereby the metal elements are adapted to respond with movement to changing environmental conditions. For example, pressure sensitive metal diaphragms incorporated in pressure switches are deformed to provide the diaphragms with a dished configuration such that the diaphragms are adapted to retain their original dished configuration under the force of selected applied fluid pressures but are adapted to move with snap-action to inverted dished configurations in response to selected greater applied fluid pressures. Similarly, bimetallic thermostatic metal discs are frequently provided with deformed portions such that the discs have selected dished configurations under one set of temperature conditions but are adapted to move with snap-action to inverted dished configurations under other temperature conditions. In such devices, these metal elements are frequently engaged with adjusting screws, stops, motion-transfer pins, other metal diaphragm elements and the like and it is found that, when the metal elements move with snap action in response to changing environmental conditions, the surfaces of the elements are sometimes abraded by such screws and the like. It is also found that even very limited abrasion of these elements significantly alters the pressure, temperature or other response characteristics of the metal elements.
It is an object of this invention to provide metal materials such as metal diaphragms and the like which are of novel and improved construction; to provide such metal materials which have adherent metal oxide coatings protecting the surfaces of the materials against abrasion; to provide novel and improved methods for making such metal materials having such metal oxide coatings; and to provide such methods which are economical to perform.
Other objects, advantages and details of the materials, elements and methods of this invention appear in the following detailed description of preferred embodiments of the invention, the detailed description referring to the drawings in which:
FIG. 1 is a diagrammatic view illustrating a preferred embodiment of the method of this invention;
FIG. 2 is a partial section view along the longitudinal axis of a strip of metal material processed according to the method of FIG. 1;
FIG. 3 is a section view along a transverse axis of a diaphragm made in accordance with this invention; and
FIG. 4 is a graph illustrating preferred parameters in the process of FIG. 1.
Referring to the drawings, FIG. 1 illustrates a preferred embodiment of the method of this invention. In this method, as shown, a metal strip is continuously fed from a pay-off reel 12 and is advanced over guide rolls 14 through a first liquid bath 16 in a vessel 18, the bath 16 being heated by any conventional means diagrammatically illustrated in FIG. 1 by the electric heater coil 20. The strip material 10 is then preferably guide rolls 14 through a secand is coiled upon a take-up advanced over additional ond bath 22 in a vessel 24 7 reel 26.
In accordance with this invention, the first process bath 16 comprises an oxidizing bath of fused alkali metal hydroxide materials which can include fused lithium, sodium or potassium hydroxide and the like alone or in combination with each other and which can also include additions of fused alkali metal nitrate and chloride salts. In a preferred embodiment of this invention, for example, the bath 16 has a composition, by weight, from about 7 to 32 percent sodium nitrate, from about 1 to 20 percent sodium chloride, and the balance sodium hydroxide, the preferred bath embodying approximately percent hydroxide, 20 percent sodium nitrate and 10 percent sodium chloride by weight.
In accordance with this invention, the bath 16 is heated to a temperature sufficient to fuse the bath ingredients and to achieve a desirable bath viscosity without heating the bath to a temperature at which the bath materials are volatilized to an excessive extent. The bath temperature is preferably kept low enough so that, at the selected speed at which the strip material 10 is advanced through the bath, the strip material is not significantly altered by such heating of the strip as will occur. Generally, advantageous strip movement speeds are such that the stress characteristics of the metal strip materials do not tend to become significantly altered in passing through the bath 16. For example, where the strip material 10 comprises any of the various commercially available stainless steels, including 300 Series and 400 Series Stainless Steel such-as Type 302 Stainless Steel having a nominal composition, by weight, of 18 percent chromium, 8 percent nickel and the balance iron, and where the bath l6 embodies 70 percent sodium hydroxide, 20 percent sodium nitrate, and 10 percent sodium chloride, the bath temperature and speed of movement of the strip 10 is preferably maintained at values falling on or between curves A and B in FIG. 4, the bath temperature and strip speed preferably being controlled in the manner indicated by curve C. That is,
the bath temperature is preferably maintained above about 650F. and at this bath temperature the strip speed is preferably regulated to provide a strip dwell time in the bath from about 30 seconds to 10 minutes and, most desirably, to provide a strip dwell time in the bath of about 4 minutes. On the other hand, where the bath temperature is maintained at about 825F., the strip speed is controlled to provide a strip dwell time in the bath of from about 8 seconds to seconds and most desirably, a dwell time of about 30 seconds.
In accordance with this invention, the metal strip material 10 should be free of any oxide scale or the like but need not be processed in any particular manner prior to immersion in the bath 16. However, it is desirable for achieving product uniformity to clean gross contaminants such as oils and greases from the strip prior to bath immersion. Such gross contaminants will be removed from the strip by immersion of the strip in the bath but for product uniformity it is desirable that all portions of the strip surface be exposed to the bath for the same period of time.
In a preferred embodiment of the process of this in vention, the strip material 10 is moved from the bath 16 through a water bath 22 for the purpose of removing any of the bath 16 which may be clinging to the strip material. The bath need not be heated but is preferably maintained at a sufficient temperature, as by the heating resulting from passage of the strip material 10 through the bath, to avoid any significant quenching or chilling of the strip material. That is, the bath 22 can be omitted if desired or can be replaced by other cleaning techniques such as by a steam bath or the like. After passing through the bath 22, if used, the strip 10 is coiled upon a take -up reel 26 in conventional manner.
In the process of this invention, the strip material 10 is altered so that the material coiled upon the take-up reel 26 comprises a metal core 10.1 of the original strip material and further embodies an adherent surface coating 10.2 of an adherent metal oxide. The coating 10.2 has a significant thickness greater than about 100 Angstrom units thickness sufficient to provide the strip material 10 with excellent abrasion-resistance properties. The coating comprises asomewhat vuniform mixture of oxides of the metals embodiedin the strip materials 10, these oxides being in relatively high oxidation states.- Where stainless steel strip materials are used, for example, the metal oxide coating 10.2 is readily visible and has a bluish green color, the coating being very hard and resistant to abrasion. The metal oxide coating is strongly adherent to the core element 10.1 such that the strip material is adapted to be subjected to temperatures over a substantial range, similar to the temperatures to which the core element material itself can withstand without tending to loosen the adherence of the metal oxide coating. The coating 10.2 is also such that the strip material 10 coated therewith is readily adapted to be deformed quite severely into a variety of configurations without tending to cause separation of the'coating from the core element 10.1. The strip materials are particularly adapted to be deformed to provide 5 In accordance with conventional procedure, the alloys set forth in this table may also include small quantities of additional constituents present as impurities in the alloys.
After providing these bimetallic strip materials with the noted metal oxide coatings, the bimetallic materials are readily cut and deformed in conventional manner to form snap-acting thermostatic elements and the like.
It will also be understood that the method of this invention can be employed for providing abrasionresistant metal'oxide coatings on diaphragm and thermostatic elements and the like which have already been formed. That is, as is illustrated in FIG. 3, a novel and improved, snap-acting stainless steel diaphragm 28 can embody a core element 28.1 formed of stainless steel, this core element being centrally deformed to provide the element with a dished configuration as shown and to permit the element to move with snap-action to an inverted dished configuration in response to application of sufficient fluid pressure force or the like to the convex side of :the element. This core element is then provided with the desired abrasion-resistant metal oxide coating 28.2 by immersing the core element in the bath 16 described with reference to FIG. 1, the temperature of the bath and dwell time of the element 28.1 in the bath being substantially the same as is employed in coating strip materials. As will be understood, thermostatic snap-acting bimetallic elements of similar construction can be coated in the same manner.
It should be understood that although particular embodiments of this invention have been described by elements of dished configuration Serve as p 35 way of illustration, this invention includes all modificaactmg Pletanlc dlaphl'agms and the llketlons and equivalents of the illustrated embodiments It will belt q the Process de scnbed which fall within the scope of the appended claims. above is useful in coating varlous metal materials and is particularly adapted for coating ferrous metal materiwe clalmf d als. It will also be understood that the process is useful 40 A f"! orrllnakmg gY snap'alctmg F] in coating bimetallic strip materials such as are convenfi comFnsmgt e S f P P "i 3 meta mater tionally used in manufacture of thermostatic elements. avmg, at east one ace t FQ formed of a For example" two or more f the metals and alloys materlal selected from the group consisting of the metvsvhqwpwjpilpablg gag pgnmgtglmrygiigqllyr P5151953? W als and alloys set forth in Table I, sald surface layer TABLE I NICKEL CHRO- IRON MANGA- ALUMI- MOLYBDE- COBALT CAR- MIUM NESE NUM NUM BON Allo B 22.0 3.0 Bal. 0.5
Alloy c 19.4 2.25 Bal.
Alloy D l4.65 Bal. 9.5 5 1 Alloy E 25.0 8.5 Bal.
Allo G 18.0 11.5 Bal.
Allo GA 18.0 10.0 Bal. 3.0
Allo 08 19.0 7.0 Ba].
Allo H 14.0 Hal. 5 0 0.5
Alloy K Bal.
Allo L 25.0 Bal. 4.0
Allo M 8.0 18.0 Bal.
Allo 32.0 Bal. 1.0 1 0 Allo 71 16.5 Bal. 4.5
Alloy ll 38.65 Bal.
Alloy 13 32.0 1 Ba]. 1.0 15.0
Allo 15 32.0 Bal. 1.0 10
Alloy 40.0 Bal.
Alloy 42.0 Bal.
Alloy 45.0 Bal.
Alloy 50.0 Bal.
Alloy 17.0 Bal.
metal material to provide said metal material with a portion of dished configuration for forming a snapacting element.
2. A method as set forth in claim 1 wherein said metal material is deformed to provide said portion of dished configuration prior to said immersion of said metal material in said fused oxidizing bath.
3. A method as set forth in claim 1 wherein said oxidizing bath comprises fused materials selected from the group consisting of alkali metal hydroxides, alkali metal nitrates and alkali metal chlorides.
4. A method as set forth in claim 3 wherein said oxidizing bath comprises, by weight, from 7 to 32 percent alkali metal nitrate, from 1 to 20 percent alkali metal chloride and the balance alkali metal hydroxide.
5. A method as set forth in claim 4 wherein said oxidizing bath comprises, by weight, approximately 70 percent sodium hydroxide, approximately 20 percent sodium nitrate, and approximately 10 percent sodium chloride. Y H V 6. A method as set forth in claim 5 wherein said fused bath is maintained at a selected temperature in the 6 range from 650 to 850 F. and said metal material is immersed in said bath for a period of time selected in accordance with FIG. 4, said time being in the range indicated by curves A and B in FIG. 4 for said selected temperature.
7. A method as set forth in claim 6 wherein said metal material comprises a multi-layer metallic material having at least one surface layer thereof formed of a metal material selected from the group of metals and alloys set forth in Table l.
8. An improved snap-acting element comprising a core formed of a metal material having at least one surface layer thereof of a material selected from the group consisting of the metals and alloys set forth in Table I, said core having at least a portion thereof of dished configuration providing said element with snap-acting properties and having an adherent metal oxide coating of at least about 100 Angstrom units thickness on said surface layer of said core providing said surface layer with improved abrasion-resistance.
9. A snap-acting element as set forth in claim 8 wherein said metal material comprises a multilayer metal material
Claims (9)
1. A METHOD FOR MAKING AN IMPROVED SNAP-ACTING ELEMENT COMPRISING THE STEPS OF PROVIDING A METAL MATERIAL HAVING AT LEAST ONE SURFACE LAYER THEREOF FORMED OF A MATERIAL SELECTED FROM THE GROUP CONSISTING OF THE METALS AND ALLOYS SET FORTH IN TABLE I, SAID SURFACE LAYER BEING FREE OF OXIDE SCALE, AND IMMERSING SAID METAL MATERIAL IN AN OXIDIZING BATH COMPRISING FUSED ALKALI METAL HYDROXIDE FOR FORMING AN ABRASION-RESISTANT METAL OXIDE COATING ON SAID SURFACE LAYER, AND DEFORMING SAID METAL MATERIAL TO PROVIDE SAID METAL MATERIAL WITH A PORTION OF DISHED CONFIGURATION FOR FORMING A SNAP-ACTING ELEMENT.
2. A method as set forth in claim 1 wherein said metal material is deformed to provide said portion of dished configuration prior to said immersion of said metal material in said fused oxidizing bath.
3. A method as set forth in claim 1 wherein said oxidizing bath comprises fused materials selected from the group consisting of alkali metal hydroxides, alkali metal nitrates and alkali metal chlorides.
4. A method as set forth in claim 3 wherein said oxidizing bath comprises, by weight, from 7 to 32 percent alkali metal nitrate, from 1 to 20 percent alkali metal chloride and the balance alkali metal hydroxide.
5. A method as set forth in claim 4 wherein said oxidizing bath comprises, by weight, approximately 70 percent sodium hydroxide, approximately 20 percent sodium nitrate, and approximately 10 percent sodium chloride.
6. A method as set forth in claim 5 wherein said fused bath is maintained at a selected temperature in the range from 650* to 850* F. and said metal material is immersed in said bath for a period of time selected in accordance with FIG. 4, said time being in the range indicated by curves A and B in FIG. 4 for said selected temperature.
7. A method as set forth in claim 6 wherein said metal material comprises a multi-layer metallic material having at least one surface layer thereof formed of a metal material selected from the group of metals and alloys set forth in Table I.
8. An improved snap-acting element comprising a core formed of a metal material having at least one surface layer thereof of a material selected from the group consisting of the metals and alloys set forth in Table I, said core having at least a portion thereof of dished configuration providing said element with snap-acting properties and having an adherent metal oxide coating of at least about 100 Angstrom units thickness on said surface layer of said core providing said surface layer with improved abrasion-resistance.
9. A snap-acting element as set forth in claim 8 wherein said metal material comprises a multilayer metal material.
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US00010533A US3847685A (en) | 1970-02-11 | 1970-02-11 | Oxide coated metal discs and method of making the same |
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US00010533A US3847685A (en) | 1970-02-11 | 1970-02-11 | Oxide coated metal discs and method of making the same |
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US3847685A true US3847685A (en) | 1974-11-12 |
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US00010533A Expired - Lifetime US3847685A (en) | 1970-02-11 | 1970-02-11 | Oxide coated metal discs and method of making the same |
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Cited By (5)
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US4131720A (en) * | 1976-04-01 | 1978-12-26 | G. Rau | Heavy-duty heat-responsive bimetallic material |
US4448611A (en) * | 1982-04-23 | 1984-05-15 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Process for improving the corrosion resistance of ferrous metal parts |
US4694558A (en) * | 1986-01-06 | 1987-09-22 | Gte Products Corporation | Bimetal thermostats and method of manufacture |
EP0667401A1 (en) * | 1994-02-09 | 1995-08-16 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Composition of salt baths based on alkali metal nitrates for oxidizing ferrous metals to improve their corrosion resistance |
WO1996034127A1 (en) * | 1995-04-28 | 1996-10-31 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Alkaline nitrate salt bath composition for oxidising a ferrous metal and improving the corrosion resistance thereof |
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US1247086A (en) * | 1915-04-03 | 1917-11-20 | Myron L Crowe | Method of coating metallic articles to prevent oxidation. |
US1879701A (en) * | 1931-11-20 | 1932-09-27 | Anthony J Marino | Protective coating and method of applying same to nickel, nickel alloys, and chromium-iron alloys |
US1895590A (en) * | 1930-06-26 | 1933-01-31 | Spencer Thermostat Co | Snap acting device |
US2479979A (en) * | 1945-07-25 | 1949-08-23 | Hooker Electrochemical Co | Processes for treating ferrous metals before drawing through dies |
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US1247086A (en) * | 1915-04-03 | 1917-11-20 | Myron L Crowe | Method of coating metallic articles to prevent oxidation. |
US1895590A (en) * | 1930-06-26 | 1933-01-31 | Spencer Thermostat Co | Snap acting device |
US1879701A (en) * | 1931-11-20 | 1932-09-27 | Anthony J Marino | Protective coating and method of applying same to nickel, nickel alloys, and chromium-iron alloys |
US2479979A (en) * | 1945-07-25 | 1949-08-23 | Hooker Electrochemical Co | Processes for treating ferrous metals before drawing through dies |
US2585704A (en) * | 1948-08-18 | 1952-02-12 | Metals & Controls Corp | Thermostat with microscopic mat finish |
US2750301A (en) * | 1952-02-04 | 1956-06-12 | Ver Deutsche Metallwerke Ag | Method of treating metallic materials |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US4131720A (en) * | 1976-04-01 | 1978-12-26 | G. Rau | Heavy-duty heat-responsive bimetallic material |
US4448611A (en) * | 1982-04-23 | 1984-05-15 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Process for improving the corrosion resistance of ferrous metal parts |
US4694558A (en) * | 1986-01-06 | 1987-09-22 | Gte Products Corporation | Bimetal thermostats and method of manufacture |
EP0667401A1 (en) * | 1994-02-09 | 1995-08-16 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Composition of salt baths based on alkali metal nitrates for oxidizing ferrous metals to improve their corrosion resistance |
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WO1996034127A1 (en) * | 1995-04-28 | 1996-10-31 | Centre Stephanois De Recherches Mecaniques Hydromecanique Et Frottement | Alkaline nitrate salt bath composition for oxidising a ferrous metal and improving the corrosion resistance thereof |
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