US3091549A - Resinous coating of siliconized iron - Google Patents
Resinous coating of siliconized iron Download PDFInfo
- Publication number
- US3091549A US3091549A US2977560A US3091549A US 3091549 A US3091549 A US 3091549A US 2977560 A US2977560 A US 2977560A US 3091549 A US3091549 A US 3091549A
- Authority
- US
- United States
- Prior art keywords
- article
- silicon
- siliconizing
- resinous material
- plugs
- 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title description 6
- 239000011248 coating agent Substances 0.000 title description 3
- 238000000576 coating method Methods 0.000 title description 3
- 229910052742 iron Inorganic materials 0.000 title description 3
- 238000005475 siliconizing Methods 0.000 claims description 21
- 229910052710 silicon Inorganic materials 0.000 claims description 17
- 239000010703 silicon Substances 0.000 claims description 17
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000012260 resinous material Substances 0.000 claims description 15
- 238000005260 corrosion Methods 0.000 claims description 11
- 230000007797 corrosion Effects 0.000 claims description 11
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 10
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 claims description 9
- 239000005049 silicon tetrachloride Substances 0.000 claims description 9
- 239000003153 chemical reaction reagent Substances 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 description 18
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 238000005470 impregnation Methods 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- 239000004809 Teflon Substances 0.000 description 5
- 229920006362 Teflon® Polymers 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 150000002739 metals Chemical class 0.000 description 4
- 239000011148 porous material Substances 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- -1 ferrous metals Chemical class 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003518 caustics Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 2
- 229910010271 silicon carbide Inorganic materials 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000025 natural resin Substances 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- RMLSRFAOCMHQKX-UHFFFAOYSA-N propan-2-one;1,1,2-trichloroethene Chemical compound CC(C)=O.ClC=C(Cl)Cl RMLSRFAOCMHQKX-UHFFFAOYSA-N 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 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
- C23C10/00—Solid state diffusion of only metal elements or silicon into metallic material surfaces
- C23C10/60—After-treatment
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C09D127/18—Homopolymers or copolymers of tetrafluoroethene
-
- 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
- Y10T428/12479—Porous [e.g., foamed, spongy, cracked, etc.]
-
- 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.]
- Y10T428/1266—O, S, or organic compound in metal 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.]
- Y10T428/12674—Ge- or Si-base 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
-
- 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
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249994—Composite having a component wherein a constituent is liquid or is contained within preformed walls [e.g., impregnant-filled, previously void containing component, etc.]
Definitions
- Metals have been protected in the past by applying to their surfaces materials having greater resistance to corrosion, chemical attack, weathering, than the metals themselves. For instance, tin, nickel, and chromium have been used to protect the metal surfaces. Well known chemical treatments, such as phosphating and siliconizing, have been employed to protect materials susceptible to corro- SlOIl.
- Typical siliconizing processes are shown in the patents of Nig, 2,109,485; Henderson et 211., 2,501,051, and Eckman, 2,897,093.
- the outer portion of the treated article is enriched in silicon.
- the ability of silicon to increase the resistance of a metal, or alloy, to corrosion, or to scaling at elevated temperatures, is well known. This is especially true of ferrous base articles.
- steel containing silicon is highly resistant to the action of corrosive substances, particularly mineral acids, such as sulfuric acid. This characteristic of high-silicon steels has been employed commercially in apparatus required to resist chemical attack.
- an object of the invention to provide a metal product having increased resistance against corrosion, rusting, or chemical attack. It is a further object of the invention to provide a protective coating which is firmly adherent and highly resistant to sustained action of many corrosive substances. Further objects and advantages of the invention will be apparent from a study of the description and the appended claims.
- the present invention relates to increasing the corrosion resistance of metal articles by contacting with a siliconizing reagent to inoculate the outer portion with silicon and form a porous surface, and then impregnating the porous surface with a synthetic resinous material.
- the invention is also related to a new article of manufacture comprising a metallic body having on the outer portion a high-silicon content and the interstices of the surface filled with a synthetic resinous material.
- FIGURE 1 is a flow sheet illustrating the process of the present invention.
- FIGURE 2 is a diagrammatical illustration in cr-oss section of an article of the present invention.
- Metals of the invention have the fullest protection against corrosion or attack by chemicals. They possess a tough surface. Moreover, the synthetic resinous material forms an anti-friction layer making the article particularly applicable to uses as bushings, valves, sleeves, liners, washers, journals, and the like which are employed in corrosive atmospheres, or surroundings.
- the siliconizing treatment may be carried out in several ways. According to the present understanding of the chemical mechanisms involved, each of the procedures forms silicon tetrachloride that reacts with the surface of the metal to form silicon, which inoculates the outer layer or portion of the article and forms a by-product chlorine gas.
- the articles receiving the siliconizing treatment are placed in a horizontal drum type retort.
- the retort is connected to a source of substantially dry inert gas, such as nitrogen, neon, or argon, which is introduced to displace the air.
- a source of substantially dry inert gas such as nitrogen, neon, or argon
- the flow of nitrogen for instance, is reduced so as to be sufiicient to make up for losses that may occur due to leakage.
- the retort is rotated and heat is applied, for example by electrical heating elements on the sides to raise the temperature to proper siliconizing levels.
- the temperatures are not critical, but generally best results are obtained at approximately 1850 F. for ordinarily low carbon steel with different temperatures for other alloys and non-ferrous metals.
- silicon tetrachloride gas is introduced into the retort. This gas is generated by applying heat to a receptacle containing liquid silicon tetrachloride.
- the silicon tetrachloride may be introduced by a carrier gas which is bubbled through the silicon tetrachloride liquid and then conducted into the retort. After the retort has filled with the siliconizing reagent, with or without the presence of the carrier, the flow of the reagent is reduced to a slow, continuous ingress for the siliconizing process.
- the exposure time of the treated articles to the siliconizing atmosphere is from about 0.5 to about five hours. Usually satisfactory results are obtained within one to three hours.
- the articles After receiving the siliconizing treatment, the articles may be allowed to cool in the retort to room temperature, or may be removed to separate containers to lower temperatures for handling.
- the Henderson Patent 2,501,051 introduces hydrogen into the treatment area.
- the Eck man Patent 2,897,093 the article is tumbled with silicon carbide so that the chlorine reacts with the silicon carbide to reduce the amount of free chlorine present.
- the porosity is increased so that in the subsequent impregnation greater amounts of the resin may be introduced.
- the articles may be reheated to high temperatures for a short period of time and then cooled in order to enlarge the openings at the surface of the articles.
- the articles are heated to 1400 F. for twenty minutes than furnace cooled overnight to open up the pores.
- the porosity may be increased by acid treatment, such as conventional etching procedures.
- the siliconized article which has been treated in the foregoing manner to produce a porous surface is impregnated with a resinous material.
- Satisfactory resinous materials which can be used in this connection are natural and synthetic resins ated from the surface of the article by subatmospheric pressures.
- the resinous material is then applied to the evacuated surface in the form of a suspension in a vaporizable carrier liquid.
- the article is next placed under atmospheric pressures, or above, and the carrier liquid evaporated to leave the resin in the intersticial surface. This cycle may be repeated until the voids are substantially filled with the resin.
- Example Two lubricated plug valve bodies were employed. The bodies were lapped to eliminate small nicks and to take down a small mound at the top of the seat where a grease ring had been located. After machining, the two plugs were siliconized. SiCl was allowed to react with the plugs for one hour and ten minutes at about 1850 F. The control bar in the siliconizing furnace was cut and case depth determined to be .0235 inch. A corner of one plug was ground off and a rough measure of case depth was estimated at .021 inch.
- the plugs were heated at 1400 F. for 20 minutes then furnace cooled overnight. This treatment successfully opened up the pores.
- the siliconized plugs were re-centered and reground to their valve bodies. Dimensions at the top of the plugs Were Diameters Depth Plug Number A of Case Before After Re- Grind- Grindmoved ing ing The grinding operation appeared to cover many of the surface pores.
- the plugs were degreased by rinsing with trichloroethylene acetone, and then immersed in a dilute (5%) HF solution in order to increase the porosity. At first bubble evolution was slow, but when more surface area was exposed, evolution was faster. The plugs were etched in this manner until fast bubble evolution had proceeded for about one minute. They were then washed in a neutralizing rinse of dilute KCN, dried in an air stream, and placed in an oven overnight.
- the plugs were allowed to cool to room temperature and then given an acetone rinse. They were then placed in vacuum for 30 minutes and impregnating emulsion (Teflon emulsion diluted with water to about 40% solids) was allowed to cover plugs as much as possible before completely removing vacuum. Covered with emulsion, the plugs were allowed to stand for 30 minutes under atmospheric pressures. After removal, the plugs were allowed to air dry, then were placed in a drying even overnight.
- emulsion Teflon emulsion diluted with water to about 40% solids
- a control piece from the control bar in the siliconizing operation was made, fired at 1400 F. for 20 minutes, surface ground, rinsed in acetone, dried in an oven and Weighed. This piece was not etched with HF as the ground surface was quite porous.
- the control piece was impregnated three times, except that it was baked at 700 F. for only 5 minutes. It was'weighed after each impregnation to determine the percent of case filled with Teflon. The case volume was measured at 0.1433 cm. (i.e. 2.09
- the method for producing a corrosion resistant ferrous article which comprises contacting a ferrous base article with a siliconizing reagent containing silicon tetrachloride at elevated temperatures and for a time sufficient to inoculate the outer portions of said article with silicon and form a porous surface, and impregnating the silicon inoculated porous surface of the article with a synthetic resinous material.
- a corrosion resistant article comprising, inoculating at least one surface of a ferrous base article with silicon by contacting with a siliconizing reagent of silicon tetrachloride at elevated temperatures and for a time sutficient to form a porous structure in the surface of said silicon inoculated article, and impregnating the porous surface of said article with a synthetic resinous material.
- the method for producing a corrosion resistant ferrous article which comprises contacting a ferrous base article with a siliconizing reagent containing silicon tetrachloride at elevated temperatures and for a time sufficient to form said article with a high silicon case having a porous surface, and impregnating said porous surface of the article with a synthetic resinous material.
- a ferrous base article having a high silicon case and a porous surface, said porous surface impregnated with a synthetic resinous material.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
May 28, 1963 J. J. KANTER 3,091,549
RESINOUS COATING OF SILICONIZED IRON Filed May 18, 1960 jZgf/ FEFROUS BASE ARTICLE THEA TMENT M/ 54' 0a,,
ATMaaPHERE J/L/CO/V/ZED FEHHOU5 5/155 ARTICLE Unite State Patented May 28, 1963 3,091,549 RESINOUS COATING OF SILICONIZED IRON Jerome J. Kanter, Palos Park, 111., assignor to Crane (30., Chicago, 111., a corporation of Illinois Filed May 18, 1960, Ser. No. 29,775 8 Ciaims. (Cl. 117-75) This invention relates as indicated to corrosion resistant metals, and more particularly, to protecting ferrous base articles.
Metals have been protected in the past by applying to their surfaces materials having greater resistance to corrosion, chemical attack, weathering, than the metals themselves. For instance, tin, nickel, and chromium have been used to protect the metal surfaces. Well known chemical treatments, such as phosphating and siliconizing, have been employed to protect materials susceptible to corro- SlOIl.
Typical siliconizing processes are shown in the patents of Ihrig, 2,109,485; Henderson et 211., 2,501,051, and Eckman, 2,897,093. In these processes the outer portion of the treated article is enriched in silicon. The ability of silicon to increase the resistance of a metal, or alloy, to corrosion, or to scaling at elevated temperatures, is well known. This is especially true of ferrous base articles. For example, it has been known for many years that steel containing silicon is highly resistant to the action of corrosive substances, particularly mineral acids, such as sulfuric acid. This characteristic of high-silicon steels has been employed commercially in apparatus required to resist chemical attack.
One disadvantage of the siliconizing processes in which the outer portion of the article is inoculated with silicon is the formation of a porous surface containing pits and voids in the surface of the treated article. The porous surface is susceptible to corrosion, chemical attack, and weathering. For this reason, siliconizing processes were developed in a direction to minimize, or reduce, the voids and pits formed during the siliconizing operation, such as shown in the Eckman patent supra. The results were, however, lessening of the depth and amount of porosity, without fully eliminating the disadvantages afforded.
It is, therefore, an object of the invention to provide a metal product having increased resistance against corrosion, rusting, or chemical attack. It is a further object of the invention to provide a protective coating which is firmly adherent and highly resistant to sustained action of many corrosive substances. Further objects and advantages of the invention will be apparent from a study of the description and the appended claims.
Briefly stated, the present invention relates to increasing the corrosion resistance of metal articles by contacting with a siliconizing reagent to inoculate the outer portion with silicon and form a porous surface, and then impregnating the porous surface with a synthetic resinous material. The invention is also related to a new article of manufacture comprising a metallic body having on the outer portion a high-silicon content and the interstices of the surface filled with a synthetic resinous material.
In the drawings:
FIGURE 1 is a flow sheet illustrating the process of the present invention; and
FIGURE 2 is a diagrammatical illustration in cr-oss section of an article of the present invention.
Metals of the invention have the fullest protection against corrosion or attack by chemicals. They possess a tough surface. Moreover, the synthetic resinous material forms an anti-friction layer making the article particularly applicable to uses as bushings, valves, sleeves, liners, washers, journals, and the like which are employed in corrosive atmospheres, or surroundings.
The siliconizing treatment may be carried out in several ways. According to the present understanding of the chemical mechanisms involved, each of the procedures forms silicon tetrachloride that reacts with the surface of the metal to form silicon, which inoculates the outer layer or portion of the article and forms a by-product chlorine gas.
According to one procedure, the articles receiving the siliconizing treatment are placed in a horizontal drum type retort. The retort is connected to a source of substantially dry inert gas, such as nitrogen, neon, or argon, which is introduced to displace the air. After the preliminary flushing, the flow of nitrogen, for instance, is reduced so as to be sufiicient to make up for losses that may occur due to leakage. Then the retort is rotated and heat is applied, for example by electrical heating elements on the sides to raise the temperature to proper siliconizing levels. The temperatures are not critical, but generally best results are obtained at approximately 1850 F. for ordinarily low carbon steel with different temperatures for other alloys and non-ferrous metals.
After the siliconizing temperature is attained, the flow of the inert gas is shut off and silicon tetrachloride gas is introduced into the retort. This gas is generated by applying heat to a receptacle containing liquid silicon tetrachloride. Alternatively, the silicon tetrachloride may be introduced by a carrier gas which is bubbled through the silicon tetrachloride liquid and then conducted into the retort. After the retort has filled with the siliconizing reagent, with or without the presence of the carrier, the flow of the reagent is reduced to a slow, continuous ingress for the siliconizing process.
Ordinarily, the exposure time of the treated articles to the siliconizing atmosphere is from about 0.5 to about five hours. Usually satisfactory results are obtained within one to three hours.
After receiving the siliconizing treatment, the articles may be allowed to cool in the retort to room temperature, or may be removed to separate containers to lower temperatures for handling.
Heretofore, various processes were developed to reduce the contact of the by-product chlorine with the metal surface. For example, the Henderson Patent 2,501,051 introduces hydrogen into the treatment area. In the Eck man Patent 2,897,093, the article is tumbled with silicon carbide so that the chlorine reacts with the silicon carbide to reduce the amount of free chlorine present. In the present process, however, it may be desirable to keep the atmosphere surrounding the treated articles as corrosive as possible to increase the porosity by producing more, and larger, voids and pits on the surface, while at the same time inoculating the outer portions with the silicon. By increasing the voids and pits, the porosity is increased so that in the subsequent impregnation greater amounts of the resin may be introduced.
Other steps may be employed for increasing the porosity, or opening the pores and voids, preparatory to the impregnation. For example, after the siliconizing operation the articles maybe reheated to high temperatures for a short period of time and then cooled in order to enlarge the openings at the surface of the articles. According to one procedure the articles are heated to 1400 F. for twenty minutes than furnace cooled overnight to open up the pores. In some instances the porosity may be increased by acid treatment, such as conventional etching procedures.
In accordance with the present invention the siliconized article which has been treated in the foregoing manner to produce a porous surface is impregnated with a resinous material. Satisfactory resinous materials which can be used in this connection are natural and synthetic resins ated from the surface of the article by subatmospheric pressures. The resinous material is then applied to the evacuated surface in the form of a suspension in a vaporizable carrier liquid. The article is next placed under atmospheric pressures, or above, and the carrier liquid evaporated to leave the resin in the intersticial surface. This cycle may be repeated until the voids are substantially filled with the resin.
The following example is given by way of illustration of the process of the invention, but it is not to be taken as limiting the methods or techniques that may be employed:
Example Two lubricated plug valve bodies were employed. The bodies were lapped to eliminate small nicks and to take down a small mound at the top of the seat where a grease ring had been located. After machining, the two plugs were siliconized. SiCl was allowed to react with the plugs for one hour and ten minutes at about 1850 F. The control bar in the siliconizing furnace was cut and case depth determined to be .0235 inch. A corner of one plug was ground off and a rough measure of case depth was estimated at .021 inch.
The plugs were heated at 1400 F. for 20 minutes then furnace cooled overnight. This treatment successfully opened up the pores.
The siliconized plugs were re-centered and reground to their valve bodies. Dimensions at the top of the plugs Were Diameters Depth Plug Number A of Case Before After Re- Grind- Grindmoved ing ing The grinding operation appeared to cover many of the surface pores.
The plugs were degreased by rinsing with trichloroethylene acetone, and then immersed in a dilute (5%) HF solution in order to increase the porosity. At first bubble evolution was slow, but when more surface area was exposed, evolution was faster. The plugs were etched in this manner until fast bubble evolution had proceeded for about one minute. They were then washed in a neutralizing rinse of dilute KCN, dried in an air stream, and placed in an oven overnight.
The plugs were allowed to cool to room temperature and then given an acetone rinse. They were then placed in vacuum for 30 minutes and impregnating emulsion (Teflon emulsion diluted with water to about 40% solids) was allowed to cover plugs as much as possible before completely removing vacuum. Covered with emulsion, the plugs were allowed to stand for 30 minutes under atmospheric pressures. After removal, the plugs were allowed to air dry, then were placed in a drying even overnight.
Next they were heated to 700 F. for minutes followed by an air cool. The excess Teflon was scraped from the plug seat surface with a wooden splint.
The impregnation operation was repeated for plug No. 2 for a total of 2 impregnation cycles. Plug No. 1 was given a total of 3 impregnation cycles.
A control piece from the control bar in the siliconizing operation was made, fired at 1400 F. for 20 minutes, surface ground, rinsed in acetone, dried in an oven and Weighed. This piece was not etched with HF as the ground surface was quite porous. The control piece was impregnated three times, except that it was baked at 700 F. for only 5 minutes. It was'weighed after each impregnation to determine the percent of case filled with Teflon. The case volume was measured at 0.1433 cm. (i.e. 2.09
cm. x 1.172 cm. x .0586 cm.).
Weight, Total Volume Percent Impreg'nations grms. increase, Teflon, Teflon gm. gm. in case Other modes of applying the principle of the invention may be employed, change being made as regards the details described, provided the features stated in any of the following claims or the equivalent of such be employed.
I, therefore, particularly point out and distinctly claim as my invention:
1. The method for producing a corrosion resistant ferrous article which comprises contacting a ferrous base article with a siliconizing reagent containing silicon tetrachloride at elevated temperatures and for a time sufficient to inoculate the outer portions of said article with silicon and form a porous surface, and impregnating the silicon inoculated porous surface of the article with a synthetic resinous material.
2. The method of claim 1 in which said synthetic resinous material is polytetnafluoroethylene.
3. In a method for producing a corrosion resistant article the steps which comprise, inoculating at least one surface of a ferrous base article with silicon by contacting with a siliconizing reagent of silicon tetrachloride at elevated temperatures and for a time sutficient to form a porous structure in the surface of said silicon inoculated article, and impregnating the porous surface of said article with a synthetic resinous material.
4. The method of claim 3 in which said synthetic resinous material is polytetrafiuoroethylene.
5. The method for producing a corrosion resistant ferrous article which comprises contacting a ferrous base article with a siliconizing reagent containing silicon tetrachloride at elevated temperatures and for a time sufficient to form said article with a high silicon case having a porous surface, and impregnating said porous surface of the article with a synthetic resinous material.
6. The method of claim 5 in which said synthetic resinous material is polytetrafluoroethylene.
7. As a new article of manufacture, a ferrous base article having a high silicon case and a porous surface, said porous surface impregnated with a synthetic resinous material.
8. The new article of claim 7 in which said synthetic resinous material is polytetrafluoroethylene.
References Cited in the file of this patent UNITED STATES PATENTS 2,897,093 Eckman July 28, 1959 2,944,917 Cahne July 12, 1960 FOREIGN PATENTS 644,167 Great Britain Oct. 4, 1950
Claims (1)
1. THE METHOD FOR PRODUCING A CORROSION RESISTANT FERROUS ARTICLE WHICH COMPRISES CONTACTING A FERROUS BASE ARRTICLE WITH A SILICONIZING REAGENT CONTAINING SILICON TETRACHLORIDE AT ELEVATED TEMPERATURES AND FOR A TIME SUFFICIENT TO INOCULATE THE OUTER PORTIONS OF SAID ARTICLE WITH SILICON AND FORM A POROUS SURFACE, AND IMPREGNATING THE SILICON INOCULATED SURFACE OF THE ARTICLE WITH SYNTHETIC RESINOUS MATERIAL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2977560 US3091549A (en) | 1960-05-18 | 1960-05-18 | Resinous coating of siliconized iron |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2977560 US3091549A (en) | 1960-05-18 | 1960-05-18 | Resinous coating of siliconized iron |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3091549A true US3091549A (en) | 1963-05-28 |
Family
ID=21850811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US2977560 Expired - Lifetime US3091549A (en) | 1960-05-18 | 1960-05-18 | Resinous coating of siliconized iron |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3091549A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257177A (en) * | 1962-05-25 | 1966-06-21 | Crane Co | Ferrous castings with siliconized inserts |
| US3765929A (en) * | 1972-03-31 | 1973-10-16 | Ibm | In situ fluorination of graphite in iron alloy |
| US4034464A (en) * | 1975-08-27 | 1977-07-12 | Ford Motor Company | Method of aluminum cylinder head valve seat coating transplant |
| US4484988A (en) * | 1981-12-09 | 1984-11-27 | Richmond Metal Finishers, Inc. | Process for providing metallic articles and the like with wear-resistant coatings |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB644167A (en) * | 1947-08-09 | 1950-10-04 | Sprague Electric Co | Improvements in electrical conductors |
| US2897093A (en) * | 1955-03-02 | 1959-07-28 | Crane Co | Process of siliconizing |
| US2944917A (en) * | 1954-12-13 | 1960-07-12 | Marc Gregoire | Method of coating a metal base with polytetrafluoroethylene |
-
1960
- 1960-05-18 US US2977560 patent/US3091549A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB644167A (en) * | 1947-08-09 | 1950-10-04 | Sprague Electric Co | Improvements in electrical conductors |
| US2944917A (en) * | 1954-12-13 | 1960-07-12 | Marc Gregoire | Method of coating a metal base with polytetrafluoroethylene |
| US2897093A (en) * | 1955-03-02 | 1959-07-28 | Crane Co | Process of siliconizing |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257177A (en) * | 1962-05-25 | 1966-06-21 | Crane Co | Ferrous castings with siliconized inserts |
| US3765929A (en) * | 1972-03-31 | 1973-10-16 | Ibm | In situ fluorination of graphite in iron alloy |
| US4034464A (en) * | 1975-08-27 | 1977-07-12 | Ford Motor Company | Method of aluminum cylinder head valve seat coating transplant |
| US4484988A (en) * | 1981-12-09 | 1984-11-27 | Richmond Metal Finishers, Inc. | Process for providing metallic articles and the like with wear-resistant coatings |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0408168B1 (en) | Method of pretreating metallic works and method of nitriding steel | |
| EP0077627B1 (en) | Corrosion resistant steel components and method of manufacture | |
| US3458353A (en) | Process of removing coatings from nickel and cobalt base refractory alloys | |
| US3091549A (en) | Resinous coating of siliconized iron | |
| US2811466A (en) | Process of chromizing | |
| CA1098254A (en) | Method for forming a carbide layer of a va group element of the periodic or chromium on the surface of a ferrous alloy article | |
| US3936583A (en) | Prevention of corrosion in metals | |
| Barbosa et al. | The surface composition and corrosion behaviour of AISI 304 stainless steel after immersion in 20% HNO3 solution | |
| US2755210A (en) | Method of treating iron or mild steel to promote the adherence of porcelain enamel, and stock so produced | |
| CA1218585A (en) | Method for surface hardening a ferrous-alloy article and the resulting product | |
| US3058206A (en) | Aluminum coating of ferrous metal and resulting product | |
| US2237314A (en) | Process of making cadmized bearings | |
| US2921877A (en) | Process of chromizing air hardening tool steel | |
| US2313754A (en) | Method of protecting magnesium and its alloys from corrosion | |
| US3455723A (en) | Coating with silicon carbide by immersion reaction | |
| JPS6221865B2 (en) | ||
| US3397092A (en) | Corrosion-resistant coatings | |
| US2857301A (en) | Method of surface-hardening steel, and a quenching medium therefor | |
| Lennon et al. | The experimental determination of potential-pH diagrams for the Ni-H2O and low alloy steel-H2O systems | |
| US1467174A (en) | Protection of iron and steel | |
| US3481769A (en) | Alloy diffusion coating process | |
| US2886463A (en) | Method of enameling mild steel | |
| US911116A (en) | Process of inlaying, ornamenting, and case-hardening metallic surfaces. | |
| US1672180A (en) | Treatment of metal surfaces | |
| US2227469A (en) | Vapor treatment of metals |