US3875777A - Reduction of copper-caused surface cracking of steel during hot-working - Google Patents
Reduction of copper-caused surface cracking of steel during hot-working Download PDFInfo
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- US3875777A US3875777A US378119A US37811973A US3875777A US 3875777 A US3875777 A US 3875777A US 378119 A US378119 A US 378119A US 37811973 A US37811973 A US 37811973A US 3875777 A US3875777 A US 3875777A
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 44
- 239000010959 steel Substances 0.000 title claims abstract description 44
- 238000005336 cracking Methods 0.000 title claims abstract description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229910052802 copper Inorganic materials 0.000 claims abstract description 38
- 239000010949 copper Substances 0.000 claims abstract description 38
- 239000011521 glass Substances 0.000 claims abstract description 32
- 238000000576 coating method Methods 0.000 claims abstract description 18
- 229910021538 borax Inorganic materials 0.000 claims abstract description 17
- 235000010339 sodium tetraborate Nutrition 0.000 claims abstract description 17
- 239000004328 sodium tetraborate Substances 0.000 claims abstract description 15
- 239000007788 liquid Substances 0.000 claims abstract description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 21
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 16
- 239000011248 coating agent Substances 0.000 claims description 13
- 239000010433 feldspar Substances 0.000 claims description 13
- 239000000377 silicon dioxide Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 238000005204 segregation Methods 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000009472 formulation Methods 0.000 claims 1
- ZDVYABSQRRRIOJ-UHFFFAOYSA-N boron;iron Chemical compound [Fe]#B ZDVYABSQRRRIOJ-UHFFFAOYSA-N 0.000 abstract description 2
- 229940108928 copper Drugs 0.000 description 33
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 10
- 229910045601 alloy Inorganic materials 0.000 description 10
- 239000000956 alloy Substances 0.000 description 10
- 238000009938 salting Methods 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 5
- 229910052742 iron Inorganic materials 0.000 description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 238000007598 dipping method Methods 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- 238000003303 reheating Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910000640 Fe alloy Inorganic materials 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000006060 molten glass Substances 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000014987 copper Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- DDSZSJDMRGXEKQ-UHFFFAOYSA-N iron(3+);borate Chemical class [Fe+3].[O-]B([O-])[O-] DDSZSJDMRGXEKQ-UHFFFAOYSA-N 0.000 description 1
- -1 iron-boron-silicon oxide Chemical compound 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D7/00—Modifying the physical properties of iron or steel by deformation
- C21D7/13—Modifying the physical properties of iron or steel by deformation by hot working
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B45/00—Devices for surface or other treatment of work, specially combined with or arranged in, or specially adapted for use in connection with, metal-rolling mills
- B21B45/02—Devices for surface or other treatment of work, specially combined with or arranged in, or specially adapted for use in connection with, metal-rolling mills for lubricating, cooling, or cleaning
- B21B45/0239—Lubricating
- B21B45/0245—Lubricating devices
- B21B45/0263—Lubricating devices using solid lubricants
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M103/00—Lubricating compositions characterised by the base-material being an inorganic material
- C10M103/06—Metal compounds
-
- 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
- C23C24/00—Coating starting from inorganic powder
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B21—MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
- B21B—ROLLING OF METAL
- B21B45/00—Devices for surface or other treatment of work, specially combined with or arranged in, or specially adapted for use in connection with, metal-rolling mills
- B21B45/02—Devices for surface or other treatment of work, specially combined with or arranged in, or specially adapted for use in connection with, metal-rolling mills for lubricating, cooling, or cleaning
- B21B45/0239—Lubricating
- B21B45/0245—Lubricating devices
- B21B45/0248—Lubricating devices using liquid lubricants, e.g. for sections, for tubes
-
- 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
- Y10S72/00—Metal deforming
- Y10S72/70—Deforming specified alloys or uncommon metal or bimetallic work
-
- 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
- Y10T29/00—Metal working
- Y10T29/49—Method of mechanical manufacture
- Y10T29/4981—Utilizing transitory attached element or associated separate material
- Y10T29/49812—Temporary protective coating, impregnation, or cast layer
Definitions
- FIG. 2 Edge of rolled plate, with coating REDUCTION OF COPPER-CAUSED SURFACE CRACKING OF STEEL DURING HOT-WORKING BACKGROUND OF THE INVENTION Steel which contains a small amount of copper is known to be hot short or brittle at temperatures at which hot-working operations such as rolling are performed. Surface cracks or imperfections which develop during hot'working continue to propagate causing failure during subsequent fabrication or use.
- copper concentrates on the surface of the steel and, because iron preferentially oxidizes, the copper remains in elemental form and does not pass into the scale formed on the steel.
- Steel is typically hot-worked at temperatures on the order of 1000 to 1300C; near or above the melting point of copper. As the copper concentrates at the surfaces of the steel and melts, it penetrates the steel surface thus weakening the surface and causing cracks to develop as hotworking is continued.
- the effect of copper on the hot shortness of steel is also dependent upon the concentration of other metals commonly present in steel. For example, if small quantities of tin are also present along with copper, the cracking observed on hot-worked steel increases markedly.
- Viscosity of the glass may be controlled by incorporating silica-containing materials such as feldspar as a component of the glass.
- Application of the glass to the steel may be accomplished by salting the steel with powdered, solid glass or by dipping the steel into molten glass.
- FIGS. 1 and 2 are photographic representations of the edges of rolled steel plates showing the reduction of surface cracking by use of glass coatings during hot-working. The figures will be discussed in more detail later.
- boron-containing glasses applied to the surface of hot steel ingots after they are stripped from the mold but before the ingots are preheated for subsequent hot-working will substantially reduce the surface cracking or hot shortness caused by segregation of copper at the steel surfaces.
- the coating ingredients melt and flow onto the surface of the oxide scale layer of the ingot.
- the glass coating penetrates and reacts with oxide scale.
- the reaction product appears to be a complex iron-boron-silicon oxide phase which prevents the formation of molten copper thus substantially reducing surface cracking during the hot-working operation.
- Boron-containing glasses useful in my invention may comprise borax glass, which is vitreous, anhydrous sodium tetraborate, or may comprise boron oxide-silica glasses.
- the latter grouping of glasses. those containing silica display higher viscosities than does borax glass and this higher viscosity is generally advantageous.
- High viscosities imparted by silica additions to borax glass tends to prevent the coating from running off an ingot before the coating reacts with scale to form less fluid iron borates and silicates during the initial stages of reheating.
- other sources of silica may be used as well.
- feldspar The proportion of feldspar to borate used depends upon the viscosity of the glass desired which in turn depends upon the specific temperature or preheat treatment being utilized. As a general rule, higher preheat temperatures require higher glass viscosities for best results. Borax glasses containing as much as 50% feldspar, corresponding to 30-35% silica, have been used with good results. Feldspar content of the boraxcontaining glasses in the range of 20 to 50% is especially useful when ingots are reheated according to a soaking pit-type reheating schedule prior to hotworking. Borax glass coatings alone without silica generally are satisfactory when using a pusher-type reheating schedule.
- Borax glass or borax-silica glass may be applied to an ingot by either dipping in molten glass or by salting.
- Salting is the application of solid, powdered glass on hot ingot surfaces. It was observed that dipping usually gave somewhat better results than salting but salting is generally a more convenient procedure. It is necessary that the ingot be at a temperature above the melting point of the glass at the time the coating is applied. In practice, temperature of the ingot should be above about 800C, preferably about 1000C, at the time the glass coating is applied.
- My process is generally applicable to those steels containing copper in a concentration whereat surface hot shortness is troublesome during hot working. This in broad terms includes those steels having copper contents ranging from about 0.25 to 1.25% copper. The precise upper and lower limits of copper content depends also upon the presence or absence in the steel of such elements as tin or nickel.
- Example 1 An alloy consisting essentially of iron and 1% copper was prepared by nonconsumable-electrode arc melting found to be present'on the surfaces of those alloy sections coated with either hydrated or anhydrous borax but copper was absent on those alloy sections coated with borax glass.
- Example 2 Alloy sections identical in composition to those of Example 1 were scaled in air at 800C for one-half hour. The sections were then coated at that temperature by salting with borax glass and with borax glass containing 25% feldspar. Coated sections were then subjected to a simulated pusher-type heating schedule which consisted of heating the specimens in burnt natural gas-air mixtures to attain a maximum temperature of 1300C in 2 to 2/2 hours. Examination of the specimens disclosed that the inner scale was very thin and that copper was present on the alloy surfaces.
- Example 3 Alloys sections identical in composition to those of Example I were scaled in air at l000C for one-half
- Example 4 lngots of an iron alloy were prepared which had the following composition: carbon, 0.18%; manganese,
- Sections of the alloy were scaled in air at I000C for one-half hour and were then coated by immersion in molten borax glass containing 25% feldspar. The coated samples were then subjected to a simulated pusher-type heating schedule as described in Example 2.
- Example 5 Alloy sections having a composition identical to those of Example 4 were scaled in air at 1000C for one-half hour and were then coated by salting with a borax glass containing 50% feldspar. The coated samples were then subjected to a simulated soaking pittype heating schedule which consisted of heating the specimens in burnt natural gas-air mixtures to reach a maximum temperature of 1300,C in 8 hours. After cooling, there was no evidence of copper segregation on the alloy surface.
- Example 6 An ingot of an iron alloy was prepared having the following composition: carbon, 0.22%; manganese. 027%; silicon, 0.19%; copper, 0.8% with the balance iron.
- the ingot was hot-stripped from the mold and one side of the ingot was coated with a glass containing sodium borate and 25% potash feldspar while the other side was left uncoated.
- the half-coated ingot was then heated in air to a temperature of 1250C over a 2-hour period and thereafter rolled to one-half thickness in 9 passes.
- FIG. 1 illustrates the appearance of the uncoated edge of the rolled plate while FIG. 2 illustrates the coated edge of the plate.
- the glass coating greatly reduced the extent of edge cracking of the rolled plate.
- a method for preventing surface cracking of steels containing from about 0.25% to 1.25% copper during hot-working, said hot-working being performed at a temperature above the melting point of copper which comprises coating the steel with a borax-containing glass prior to the hot working in an amount sufficient to prevent the formation and segregation of liquid cop-' per at the steel surface.
- boraxcontaining glass is a mixture of vitreous, anhydrous, sodium tetraborate and a silica-containing compound.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Joining Of Glass To Other Materials (AREA)
Abstract
Steels containing small amounts of copper display surface hot shortness or cracking during hot-working caused by molten copper segregating at the steel surfaces. Coatings of borax-containing glass applied to steel prior to hot-working react with scale to form various iron-boron phases which inhibit the occurrence of liquid copper at the steel surface.
Description
United States Patent 1 [111 3,875,777
Kelley 1 Apr. 8, 1975 [5 REDUCTION OF COPPER-CAUSED 3.125519 3/1964 Grave et al. 72/42 SURFACE CRACKING OF STEEL DURING 3.295.346 1/1967 Bomberger et al. t. 72/4] 3.382.700 5/1968 Heitmann et al. 72/700 x HOT-WORKING Inventor: John E. Kelley, Star Rt. 2. Box 38 AC, Philomath. Oreg. 97370 Filed: July 11, 1973 Appl. No.: 378,119
US. Cl. 72/46: 29/424; 72/700 Int. Cl. 8210 23/24 Field of Search 72/41. 42, 46, 47, 700;
References Cited UNITED STATES PATENTS Primary E.\'umim'rC. W. Lanham Assistant E.\'aminerE. M. Combs Attorney. Agent, or FirmRoland H. Shubert: Gersten Sadowsky [57] ABSTRACT Steels containing small amounts of copper display surface hot shortness or cracking during hot-working caused by molten copper segregating at the steel surfaces. Coatings of borax-containing glass applied to steel prior to hot-working react with scale to form various iron-boron phases which inhibit the occurrence of liquid copper at the steel surface.
6 Claims, 2 Drawing Figures See le,
Edge of rolled plate, with coating inches PATENTEDAPR 81975 3,875,777 Q Scale, inches Edge of rolled plate, without coating Sco le, inches FIG. 2 Edge of rolled plate, with coating REDUCTION OF COPPER-CAUSED SURFACE CRACKING OF STEEL DURING HOT-WORKING BACKGROUND OF THE INVENTION Steel which contains a small amount of copper is known to be hot short or brittle at temperatures at which hot-working operations such as rolling are performed. Surface cracks or imperfections which develop during hot'working continue to propagate causing failure during subsequent fabrication or use.
During hot-working, copper concentrates on the surface of the steel and, because iron preferentially oxidizes, the copper remains in elemental form and does not pass into the scale formed on the steel. Steel is typically hot-worked at temperatures on the order of 1000 to 1300C; near or above the melting point of copper. As the copper concentrates at the surfaces of the steel and melts, it penetrates the steel surface thus weakening the surface and causing cracks to develop as hotworking is continued. The effect of copper on the hot shortness of steel is also dependent upon the concentration of other metals commonly present in steel. For example, if small quantities of tin are also present along with copper, the cracking observed on hot-worked steel increases markedly. On the other hand, the presence of nickel in association with copper decreases the sensitivity of steel to surface cracking. A discussion of the influence of residual elements on the surface hot shortness of steel is found in the Journal of the Iron and Steel Institute, Vol. 200, pages 290-299, April 1962.
Much iron and steel scrap, especially that derived from automobiles, contains significant amounts of cop per. This scrap is generally unsatisfactory for use as a blast furnace charge unless provisions are made for either removing the copper from the scrap before melting or adding nickel or like metals to the charge so as to avoid the detrimental effect of copper. Both approaches are generally so expensive as to be economically prohibitive.
SUMMARY OF THE INVENTION Surface cracking of copper-containing steels during hot-working is substantially reduced or prevented by coating the steel prior to hot-working with a boraxcontaining glass. Viscosity of the glass may be controlled by incorporating silica-containing materials such as feldspar as a component of the glass. Application of the glass to the steel may be accomplished by salting the steel with powdered, solid glass or by dipping the steel into molten glass.
Hence, it is an object of my invention to control the surface hot shortness of copper-containing steels.
It is a further object of my invention to provide coatings for steel which prevent the occurrence of liquid copper at the steel surface during hot-working.
It is yet another object of my invention to provide a technique which allows the use of copper-containing scrap in the manufacture of steel.
DETAILED DESCRIPTION OF THE INVENTION Results obtainable by practice of my invention are illustrated by FIGS. 1 and 2 which are photographic representations of the edges of rolled steel plates showing the reduction of surface cracking by use of glass coatings during hot-working. The figures will be discussed in more detail later.
l have found that boron-containing glasses applied to the surface of hot steel ingots after they are stripped from the mold but before the ingots are preheated for subsequent hot-working will substantially reduce the surface cracking or hot shortness caused by segregation of copper at the steel surfaces. The coating ingredients melt and flow onto the surface of the oxide scale layer of the ingot. As the ingot is further heated to the maximum preheat temperature, generally on the order of ll to l300C, the glass coating penetrates and reacts with oxide scale. The reaction product appears to be a complex iron-boron-silicon oxide phase which prevents the formation of molten copper thus substantially reducing surface cracking during the hot-working operation.
Boron-containing glasses useful in my invention may comprise borax glass, which is vitreous, anhydrous sodium tetraborate, or may comprise boron oxide-silica glasses. The latter grouping of glasses. those containing silica, display higher viscosities than does borax glass and this higher viscosity is generally advantageous. High viscosities imparted by silica additions to borax glass tends to prevent the coating from running off an ingot before the coating reacts with scale to form less fluid iron borates and silicates during the initial stages of reheating. I particularly prefer to use feldspar as a silica source in combination with sodium borate. However, other sources of silica may be used as well.
The proportion of feldspar to borate used depends upon the viscosity of the glass desired which in turn depends upon the specific temperature or preheat treatment being utilized. As a general rule, higher preheat temperatures require higher glass viscosities for best results. Borax glasses containing as much as 50% feldspar, corresponding to 30-35% silica, have been used with good results. Feldspar content of the boraxcontaining glasses in the range of 20 to 50% is especially useful when ingots are reheated according to a soaking pit-type reheating schedule prior to hotworking. Borax glass coatings alone without silica generally are satisfactory when using a pusher-type reheating schedule.
Borax glass or borax-silica glass may be applied to an ingot by either dipping in molten glass or by salting. Salting, as the term is used here, is the application of solid, powdered glass on hot ingot surfaces. It was observed that dipping usually gave somewhat better results than salting but salting is generally a more convenient procedure. It is necessary that the ingot be at a temperature above the melting point of the glass at the time the coating is applied. In practice, temperature of the ingot should be above about 800C, preferably about 1000C, at the time the glass coating is applied.
My process is generally applicable to those steels containing copper in a concentration whereat surface hot shortness is troublesome during hot working. This in broad terms includes those steels having copper contents ranging from about 0.25 to 1.25% copper. The precise upper and lower limits of copper content depends also upon the presence or absence in the steel of such elements as tin or nickel.
The following examples serve to more fully illustrate specific embodiments of my process.
Example 1 An alloy consisting essentially of iron and 1% copper was prepared by nonconsumable-electrode arc melting found to be present'on the surfaces of those alloy sections coated with either hydrated or anhydrous borax but copper was absent on those alloy sections coated with borax glass.
Example 2 Alloy sections identical in composition to those of Example 1 were scaled in air at 800C for one-half hour. The sections were then coated at that temperature by salting with borax glass and with borax glass containing 25% feldspar. Coated sections were then subjected to a simulated pusher-type heating schedule which consisted of heating the specimens in burnt natural gas-air mixtures to attain a maximum temperature of 1300C in 2 to 2/2 hours. Examination of the specimens disclosed that the inner scale was very thin and that copper was present on the alloy surfaces.
Example 3 Alloys sections identical in composition to those of Example I were scaled in air at l000C for one-half Example 4 lngots of an iron alloy were prepared which had the following composition: carbon, 0.18%; manganese,
0.45%; silicon, 0.28%; and 'copper 1.0 9%. Sections of the alloy were scaled in air at I000C for one-half hour and were then coated by immersion in molten borax glass containing 25% feldspar. The coated samples were then subjected to a simulated pusher-type heating schedule as described in Example 2.
After cooling, metallographic examination showed no evidence of copper segregation at the alloy surfaces. Retention of borax as complex phases in the inner scale was demonstrated by microprobe analysis as set out in the following table.
Example 5 Alloy sections having a composition identical to those of Example 4 were scaled in air at 1000C for one-half hour and were then coated by salting with a borax glass containing 50% feldspar. The coated samples were then subjected to a simulated soaking pittype heating schedule which consisted of heating the specimens in burnt natural gas-air mixtures to reach a maximum temperature of 1300,C in 8 hours. After cooling, there was no evidence of copper segregation on the alloy surface.
Example 6' An ingot of an iron alloy was prepared having the following composition: carbon, 0.22%; manganese. 027%; silicon, 0.19%; copper, 0.8% with the balance iron. The ingot was hot-stripped from the mold and one side of the ingot was coated with a glass containing sodium borate and 25% potash feldspar while the other side was left uncoated. The half-coated ingot was then heated in air to a temperature of 1250C over a 2-hour period and thereafter rolled to one-half thickness in 9 passes.
FIG. 1 illustrates the appearance of the uncoated edge of the rolled plate while FIG. 2 illustrates the coated edge of the plate. As is evident from a comparison of the figures, the glass coating greatly reduced the extent of edge cracking of the rolled plate.
I claim:
1. A method for preventing surface cracking of steels containing from about 0.25% to 1.25% copper during hot-working, said hot-working being performed at a temperature above the melting point of copper, which comprises coating the steel with a borax-containing glass prior to the hot working in an amount sufficient to prevent the formation and segregation of liquid cop-' per at the steel surface.
2. The method of claim 1 wherein the boraxcontaining glass is applied to the steel ata temperature above about 800C.
3. The process of claim 2 wherein the boraxcontaining glass is vitreous, anhydrous, sodium tetraborate.
4. The process of claim 1 wherein the boraxcontaining glass is a mixture of vitreous, anhydrous, sodium tetraborate and a silica-containing compound.
5. The process of claim 4 wherein the silicacontaining compound is feldspar.
6. The process of claim 5'wherein the feldspar content of the borax-containing glass is in the range of 20 to 50%.
TABLE Content. weight percent Probable phase Phase color Fe Si Na B 0 Mn or complex Light brown 78.0 0.5 L0 2.0 22.0 0.? FeO Steel gray 64.5 0.5 L0 5.0 3L0 0.2 Fe B. ,O I Dark 30.0 19.0 8.0 4.0 36.0 0.9 Nfl O.FCO.2slO- ,.B O
Claims (6)
1. A METHOD FOR PREVENTING SURFACE CRACKING OF STEELS CONTAINING FROM ABOUT 0.25% TO 1.25% COPPER DURING HOTWORKING, SAID HOT-WORKING BEING PERFORMED AT A TEMPERATURE ABOVE THE MELTING POINT OF COPPER, WHICH COMPRISES COATING THE STEEL WITH A BORAX-CONTAINING GLASS PRIOR TO THE HOT WORKING IN AN AMOUNT SUFFICIENT TO PREVENT THE FORMULATION AND SEGREGATION OF LIQUID COPPER AT THE STEEL SURFACE.
2. The method of claim 1 wherein the borax-containing glass is applied to the steel at a temperature above about 800.degree.C.
3. The process of claim 2 wherein the borax-containing glass is vitreous, anhydrous, sodium tetraborate.
4. The process of claim 1 wherein the borax-containing glass is a mixture of vitreous, anhydrous, sodium tetraborate and a silica-containing compound.
5. The process of claim 4 wherein the silica-containing compound is feldspar.
6. The process of claim 5 wherein the feldspar content of the borax-containing glass is in the range of 20 to 50%.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US378119A US3875777A (en) | 1973-07-11 | 1973-07-11 | Reduction of copper-caused surface cracking of steel during hot-working |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US378119A US3875777A (en) | 1973-07-11 | 1973-07-11 | Reduction of copper-caused surface cracking of steel during hot-working |
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US3875777A true US3875777A (en) | 1975-04-08 |
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Application Number | Title | Priority Date | Filing Date |
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US378119A Expired - Lifetime US3875777A (en) | 1973-07-11 | 1973-07-11 | Reduction of copper-caused surface cracking of steel during hot-working |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5041188A (en) * | 1989-03-02 | 1991-08-20 | Santa Barbara Research Center | High temperature superconductor detector fabrication process |
US5333415A (en) * | 1991-03-01 | 1994-08-02 | Aerospace Systems & Technologies Ltd. | Process for sealing a perforated web material |
CN108192390A (en) * | 2018-01-20 | 2018-06-22 | 中北大学 | Steel-copper solid-liquid bimetal composite casting high-temp antioxidizing paint |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2538917A (en) * | 1941-11-22 | 1951-01-23 | Comptoir Ind Etirage | Extrusion of metals |
US2968092A (en) * | 1956-02-13 | 1961-01-17 | Yawata Iron & Steel Co | Process of working steel for preventing surface defects thereof |
US3125519A (en) * | 1956-05-16 | 1964-03-17 | Lubricants | |
US3295346A (en) * | 1964-02-11 | 1967-01-03 | Crucible Steel Co America | Methods for the elevated temperature protection of metallic surface, and coatings therefor |
US3382700A (en) * | 1966-03-31 | 1968-05-14 | Inland Steel Co | Process for reducing surface checking during hot working of steel |
-
1973
- 1973-07-11 US US378119A patent/US3875777A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2538917A (en) * | 1941-11-22 | 1951-01-23 | Comptoir Ind Etirage | Extrusion of metals |
US2968092A (en) * | 1956-02-13 | 1961-01-17 | Yawata Iron & Steel Co | Process of working steel for preventing surface defects thereof |
US3125519A (en) * | 1956-05-16 | 1964-03-17 | Lubricants | |
US3295346A (en) * | 1964-02-11 | 1967-01-03 | Crucible Steel Co America | Methods for the elevated temperature protection of metallic surface, and coatings therefor |
US3382700A (en) * | 1966-03-31 | 1968-05-14 | Inland Steel Co | Process for reducing surface checking during hot working of steel |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5041188A (en) * | 1989-03-02 | 1991-08-20 | Santa Barbara Research Center | High temperature superconductor detector fabrication process |
US5333415A (en) * | 1991-03-01 | 1994-08-02 | Aerospace Systems & Technologies Ltd. | Process for sealing a perforated web material |
CN108192390A (en) * | 2018-01-20 | 2018-06-22 | 中北大学 | Steel-copper solid-liquid bimetal composite casting high-temp antioxidizing paint |
CN108192390B (en) * | 2018-01-20 | 2019-11-29 | 中北大学 | Steel-copper solid-liquid bimetal composite casting high-temp antioxidizing paint |
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