US2250488A - Cast iron and a method of producing chilled surfaces thereon - Google Patents
Cast iron and a method of producing chilled surfaces thereon Download PDFInfo
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- US2250488A US2250488A US223322A US22332238A US2250488A US 2250488 A US2250488 A US 2250488A US 223322 A US223322 A US 223322A US 22332238 A US22332238 A US 22332238A US 2250488 A US2250488 A US 2250488A
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- tellurium
- iron
- chilled
- chill
- casting
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- 238000000034 method Methods 0.000 title description 18
- 229910001018 Cast iron Inorganic materials 0.000 title description 16
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 68
- 229910052714 tellurium Inorganic materials 0.000 description 68
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 67
- 238000005266 casting Methods 0.000 description 51
- 229910052742 iron Inorganic materials 0.000 description 34
- 229910001060 Gray iron Inorganic materials 0.000 description 23
- 229910052751 metal Inorganic materials 0.000 description 18
- 239000002184 metal Substances 0.000 description 18
- 239000000203 mixture Substances 0.000 description 12
- 238000004519 manufacturing process Methods 0.000 description 9
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000000576 coating method Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 229910001037 White iron Inorganic materials 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910001215 Te alloy Inorganic materials 0.000 description 2
- 229910001567 cementite Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 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 2
- 239000000155 melt Substances 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 230000000087 stabilizing effect Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 235000002568 Capsicum frutescens Nutrition 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003467 diminishing effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 238000007528 sand casting Methods 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 150000004772 tellurides Chemical class 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22C—FOUNDRY MOULDING
- B22C3/00—Selection of compositions for coating the surfaces of moulds, cores, or patterns
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D27/00—Treating the metal in the mould while it is molten or ductile ; Pressure or vacuum casting
- B22D27/18—Measures for using chemical processes for influencing the surface composition of castings, e.g. for increasing resistance to acid attack
Definitions
- Race-1895' Our invention relates to cast iron and a method of producing chilled surfaces thereon. It has to do, more particularly, with a method of producing a hard chilled surface on gray iron castings.
- Still another method for producing chilled surfaces on gray iron castings has been to adjust the composition of the iron very closely with regard to silicon, carbon and sulfur contents and to use certain carbide stabilizing elements such as chromium and vanadium.
- carbide stabilizing elements such as chromium and vanadium.
- chilled, wear-resistant surfaces have been formed on castings without the aid of metal chills.
- This practice has had limited application because of difliculty in regulating iron compositions and has thus been suitable for a. few types of castings only. Even when production conditions are favorable to the use of this practice, the resultant chilled surfaces are frequently mottled, that is, they consist of gray and white areas and are, therefore, not fully hardened.
- metal chills for producing chilled surfaces on gray iron castings. It is difficult, for example, to use suchchills when the section of the casting is light. Furthermore, metal chills can be used only where it is possible to remove them from the solidified castings; otherwise they are lost. The making of metal chills is expensive, and unless they can be used over and over again a large number of times, it is not economical and feasible to use them. The high cost of metal chills is particularly evident in the making of a single casting or only a few castings from a. pattern. The full cost of the metal chill or chills must be borne in the casting price, and in this case it becomes an item of considerable expense. Metal chills also require frequent attention in order to keep them in good condition and to keep their surfaces from oxidizing -and rusting. Finally, the depth of chill obtained in this manof metal chills.
- Another object of our invention is to provide a method of producing chilled surfaces on cast iron wherein'the depth of chill can be controlled :vithout altering the basic composition of the run.
- Another object of our invention is to provide an improved chilled gray iron which is particularly suitable for use in the manufacture of wearresistant objects.
- Chilled surfaces produced by adding tellurium to the molten iron are uniform in depth and are usually distinguished from chills obtained by other practices by the fact that they rarely show a mottled zone between the chill and the gray interior.
- the transition from white to gray structure is usually quite sharp. In spite of this sharpness of contact between the chill and gray interior, the chills so formed resist spelling against thermal and mechanical shock to a marked degree.
- the depth of chill formed in accordance with our invention is determined largely by the size of the casting, by the composition of the iron, by the duration of time between the introduction of the tellurium in the iron and the pouring of the casting, and by the amount of tellurium used.
- the size of the casting affects the rate of the cooling and consequently a decrease in the size of sections of the casting decreases the amount of tellurium required for a given depth of chill. If the cast iron has other elements therein which iron to produce the desired chill adjacent the surface of the casting.
- Tellurium-containln coatings have been applied as mold washes which can be sprayed or painted on the mold, as dry powder which can be dusted on the maid, and as a material applied to the pattern which subsequently can be transferred to the mold when it is being made.
- Another method of application not as effective as these above mentioned, but
- tellurium helps to stabilize the cementite, less tellurium' will be required for a given depth of chill, while with more strongly graphitizing cast iron, more tellurium will be required.
- tellurium diminishes as the time, from the moment it is added to the melt to the time of pouring the casting, increases. Thus, the time factor must be given consideration. Vaporization of the tellurium from the melt is probably responsible for its diminishing effect with time. Proper chill depths are obtainable by control of these various factors. Even though the castings are large, the
- Chilled cast iron is usually more resisttellurium and retarding its penetration into the iron, permitting the metal to flow and fill the mold beforethe tellurium became thoroughly active.
- a measure of the quantity of tellurium, deposited on the mold surface, that has been employed successfully for the production of local chilled areas on castings can be gained from sometests conducted on automotive cam shafts.
- the tips and surfaces of cams were chilled by spraying the surface of the cam cavities in the mold with a light coating of tellurium-bearing wash.
- the amount of tellurium used per square inch of manner have hardness similar to those of chilled surfaces produced with metal chills.
- the production of localized chilled areas on gray iron castings can also be efiected by using tellurium-coated-inserts in the mold made up from .wire, nails, or other ferrous materials, and casting the iron about the inserts.
- These coated inserts may be prepared by hot-dipping in molten tellurium or tellurium alloys. Light inserts of this kind in the molds melt and disappear in the hot iron and permit the tellurium: to act upon the iron, forming chilled areas in the vicinity. Very satisfactory localized chilled areas are obtained in this manner with small quantities of tellurium. For chilling the tip and surface of a cam on a cast iron cam shaft, it was found that 0.02 to 0.06 gram per square inch of tellurium on an insert was sufficient.
- resultant chilled layer immediately adjacent the surface of the casting will be characterized by the presence of tellurium in an amount rangingfrom 0.001 per cent to 0.5 per cent.
- Our invention provides a practical way to improve the resistance of gray iron castings to atmospheric corrosion and to corrosion in some ant to atmospheric andacid corrosion than gray iron, so that improved resistance is obtained by surfacing gray iron castings with a chill.
- the effect of the chilled surface was determined as follows: Specimens 1 inch x '3 inches x 1; inch of gray iron whose surfaces were and were not chilled by tellurium were totally immersed in 2 per cent sulfuric acid and 2 per cent hydrochloric acid for-26 hours, the acids being renewed every 1 hours. Weight losses in grams in these two acids after immersion were:
- Our invention of utilizing tellurium and tellurium-bearing materials to provide chilled surfaces and localized chilled areas on gray iron castings is suitable for a wide range-of applications.
- Articles such as cams on cast iron camshafts, teeth on cast iron gears, various castings on agricultural equipment, cast iron paving blocks, sections of cast iron roofing, and other cast iron articles requiring resistance to wear, abrasion, or corrosion are examples where our invention is applicable.
- tellurium is used in the following claims, alloys of tellurium and compounds and other materials containing tellurium are also included.
- a method of forming chilled surfaces on a gray iron casting which comprises applying tellurium to the surface of a mold cavity and then pouring the iron into such mold cavity, the tellurium being applied to the surface of the mold cavity, in an amount suflicient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent.
- a method of forming chilled surfaces on a gray iron casting comprising the application of a mold wash containing tellurium to-the surface of a mold cavity and then pouring the iron therein, the mold wash containing tellurium in an amount sufficient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent.
- a method of forming chilled surfaces on a gray iron casting which comprises the application of from 0.005 gram to 0.3 gram of tellurium to each square inch of surface of a mold cavity and then pouring the iron therein.
- a method of forming localized chilled surface areas on a gray iron casting comprising the coating of the surface of the mold cavity with tellurium at such locations corresponding to the areas of localized chill on the casting, then pouring the iron therein, the tellurium being applied to the surface of the mold cavity in an amount sufiicient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent.
- a wear-resistant cast iron article comprising a layer oi! chilled iron on a gray iron casting, said chilledironlayer being characterized by the presence 01' tellurium in an amount ranging irom 0.001 per cent to 0.5 per cent.
- a cast iron the basic composition or which without a-tellurium content would normally be from gray to mottled if cast without chilling, said cast iron having a hard wear-resistant surface and containing tellurium in eflective amount in said surtacecaullngit tobehardandwhiteand greater in percentage as compared with the interior of the same.
- a method of forming chilled surfaces on a gray iron casting which comprises applying tellurium to the surface of a mold cavity and then pouring the iron into such mold cavity. the tcllurium being applied to the surface of the mold cavity in an amount aumcient to produce a chilled iron layer adjacent the surface oi the casting. 4
Description
Patented July 2 9, 1941 UNITED STATES PATENT OFFICE CAST IRON AND A METHOD OF PRODUCING GHILLED SURFACES THEREON Clarence n. Lorigm Daniel E. Kraule, Columbus, Ohio, assignors to-Battclle Memorial Institute, Columbus, Ohio, a corporation! Ohio N marina: Application mime '5, 193:,
Serial no. 223,322
realms. (race-1895' Our invention relates to cast iron and a method of producing chilled surfaces thereon. It has to do, more particularly, with a method of producing a hard chilled surface on gray iron castings.
In the art of providing chilled surfaces on grayiron castings. it is general knowledge that one of the oldest and still widely used methods is-to embed a metal chill in the mold corresponding in location to the area or surface desired to be hardened. A hard surface is thus produced by casting the metal against the chill, in which case, the metal chill extracts heat from the contacting metal at a rate which causes it to solidify at the surface and to some depth beneath the surface as white iron. The carbon in the iron which normally is present as soft graphite in gray iron Another object of our invention is toprovide a method of producing localized hard chilled surface areas on gray iron castings without the use castings exists as inter-dendritic masses of car- 1 bide in the area adjacent to the metal chill.
Still another method for producing chilled surfaces on gray iron castings has been to adjust the composition of the iron very closely with regard to silicon, carbon and sulfur contents and to use certain carbide stabilizing elements such as chromium and vanadium. With precise control of composition, chilled, wear-resistant surfaces have been formed on castings without the aid of metal chills. This practice, however, has had limited application because of difliculty in regulating iron compositions and has thus been suitable for a. few types of castings only. Even when production conditions are favorable to the use of this practice, the resultant chilled surfaces are frequently mottled, that is, they consist of gray and white areas and are, therefore, not fully hardened.
There are also certain limitations in the use of metal chills for producing chilled surfaces on gray iron castings. It is difficult, for example, to use suchchills when the section of the casting is light. Furthermore, metal chills can be used only where it is possible to remove them from the solidified castings; otherwise they are lost. The making of metal chills is expensive, and unless they can be used over and over again a large number of times, it is not economical and feasible to use them. The high cost of metal chills is particularly evident in the making of a single casting or only a few castings from a. pattern. The full cost of the metal chill or chills must be borne in the casting price, and in this case it becomes an item of considerable expense. Metal chills also require frequent attention in order to keep them in good condition and to keep their surfaces from oxidizing -and rusting. Finally, the depth of chill obtained in this manof metal chills.
Another object of our invention is to provide a method of producing chilled surfaces on cast iron wherein'the depth of chill can be controlled :vithout altering the basic composition of the run.
Another object of our invention is to provide an improved chilled gray iron which is particularly suitable for use in the manufacture of wearresistant objects.
Other objects and advantages of our invention will become apparent from the following description and claims. fi/
We have found a novel and inexpensive method for producing a hard, chilled surface on gray iron castings that overcomes the limitations of the prior art. By using small quantities of tellurium either in the iron composition or on the mold surface, or by introducing minute amounts of tellurium into the iron at the point where chill is desired, we have found it possible to effect strong general and local chilling tendencies in iron castings. In its effect, tellurium is extremely potent, and in such instances where it is not introduced directly to the iron but is placed in the mold for localized chilling, its sphere of influence extends a substantial though limited distance beyond the point where it contacts the iron. Chilled surfaces not only can be localized if desired, but the depth of chili can be varied merely by varying the amount of tellurium used. While the amount of tellurium required to effect various chill depths depends upon the composition of the iron and the size of the casting, our invention makes possible the control of chill depth for any gray iron composition or for any size of casting by the use of varying amounts of tellurium.
The effectiveness of tellurium in forming white iron was demonstrated by adding small quantities to a gray iron melt containing 2.65 per cent carbon, 2.00 per cent silicon, 0.40 per cent manganese, 0.15 per cent phosphorus, and 0.036 per cent sulfur. The iron cast into sections of different thicknesses gave chill results as follows:
In these tests, with an iron of low carbon contentfthe potency of 0.025 per cent tellurium was indicated by the stabilizing of cementite in sections as large as 1 inch. If insuflicienttellurium is added to iron to produce an entirely white iron, we have found that a casting is obtained having a white shell or chill of uniform thickness with a gray iron interior. This was illustrated with wedges cast in sand from heats whose base composition was 3.30 per cent carbon, 1.70 per cent silicon, 0.50 per cent chromium, 0.60 per cent manganese, and 0.07 per cent sulfur. The crosssection of the wedges was triangular with two sides 1% inches long and the third side inch long. A wedge from metal containing no tellurium showed no chill. On adding 0.02 per cent tellurium, a chill approximately inch in depth surrounded the wedge, while with 0.028 per cent tellurium the chill depth was increased to approximately inch. With 0.045 per cent tellurium the entire section was white.
Chilled surfaces produced by adding tellurium to the molten iron are uniform in depth and are usually distinguished from chills obtained by other practices by the fact that they rarely show a mottled zone between the chill and the gray interior. The transition from white to gray structure is usually quite sharp. In spite of this sharpness of contact between the chill and gray interior, the chills so formed resist spelling against thermal and mechanical shock to a marked degree.
The depth of chill formed in accordance with our invention is determined largely by the size of the casting, by the composition of the iron, by the duration of time between the introduction of the tellurium in the iron and the pouring of the casting, and by the amount of tellurium used. The size of the casting affects the rate of the cooling and consequently a decrease in the size of sections of the casting decreases the amount of tellurium required for a given depth of chill. If the cast iron has other elements therein which iron to produce the desired chill adjacent the surface of the casting.
Another effective method for producing chill either over the entire surface or at localised .areasonagrayironcastingistocoatthemold tion of the tellurium. Tellurium-containln coatings have been applied as mold washes which can be sprayed or painted on the mold, as dry powder which can be dusted on the maid, and as a material applied to the pattern which subsequently can be transferred to the mold when it is being made. Another method of application not as effective as these above mentioned, but
help to stabilize the cementite, less tellurium' will be required for a given depth of chill, while with more strongly graphitizing cast iron, more tellurium will be required. The effect of tellurium diminishes as the time, from the moment it is added to the melt to the time of pouring the casting, increases. Thus, the time factor must be given consideration. Vaporization of the tellurium from the melt is probably responsible for its diminishing effect with time. Proper chill depths are obtainable by control of these various factors. Even though the castings are large, the
' iron strongly graphitizing, and the time before pouring after the introduction of tellurium long, we have found that it requires substantially less than 1 per cent tellurium to produce chilled surfaces on sand castings. We prefer to add from 0.001 per cent to 0.5 per cent tellurium to the nevertheless practical, ,is to add the tellurium or tellurium-containing substance to facing sand used to cover such portions of the pattern where chilled surfaces are to be formed on thecastinss.
In producing chilled areas by application to the mold surface, the most satisfactory method found for controlling the depth of chill was to vary the tellurium concentration on the mold surface.
Our preferred method of coating mold surfaces with tellurium-bearing material is to incorporate the tellurium in a sprayable mold wash. Various washes have been prepared and used successfully. Typical compositions of such mold washes as were used are:
We employed kerosene in many wash mixtures to decrease the water content and to provide a kerosene water emulsion for suspending the tellurium, tellurides, tellurates or other tellurium I compounds which normally settle rapidly in watellurium by the iron and to restrict the sphere.
of influence of the tellurium, an important'factor when the chill is to be localized. Such material proved effective in momentarily protecting the -2,25o,4aa
acids. Chilled cast iron is usually more resisttellurium and retarding its penetration into the iron, permitting the metal to flow and fill the mold beforethe tellurium became thoroughly active.
A measure of the quantity of tellurium, deposited on the mold surface, that has been employed successfully for the production of local chilled areas on castings can be gained from sometests conducted on automotive cam shafts. The tips and surfaces of cams were chilled by spraying the surface of the cam cavities in the mold with a light coating of tellurium-bearing wash.
, The amount of tellurium used per square inch of manner have hardness similar to those of chilled surfaces produced with metal chills.
The production of localized chilled areas on gray iron castings can also be efiected by using tellurium-coated-inserts in the mold made up from .wire, nails, or other ferrous materials, and casting the iron about the inserts. These coated inserts may be prepared by hot-dipping in molten tellurium or tellurium alloys. Light inserts of this kind in the molds melt and disappear in the hot iron and permit the tellurium: to act upon the iron, forming chilled areas in the vicinity. Very satisfactory localized chilled areas are obtained in this manner with small quantities of tellurium. For chilling the tip and surface of a cam on a cast iron cam shaft, it was found that 0.02 to 0.06 gram per square inch of tellurium on an insert was sufficient.
When the chill is produced by applying tellurium to the mold surface or to the insert, the
, resultant chilled layer immediately adjacent the surface of the casting will be characterized by the presence of tellurium in an amount rangingfrom 0.001 per cent to 0.5 per cent. V
An inexpensive method for producing hard, chilled surfaces on gray'iron castings is thus provided by our invention. Chills can be localized with ease, if necessary. Because the quantity of tellurium used is small, the cost of the tellurium itself is negligible. The various methods used in applying tellurium or its compounds in accordance with our invention are also inexpensive. Besides being very simple and inexpensive, our process is flexible and is readily adapted to castings having surface contours that prohibit obtaining desired results with metal chills.
Further economies over present practices prevail in surface chilling castings where only one or a few are made from a pattern. The preparation of metal chills is dispensed with so that the cost of making the castings, whether the iron is alloyed with tellurium or whether tellurium is applied to the mold, is relatively no more than if the castings were made without the chill. Considerable savings in time are also involved.
Our invention provides a practical way to improve the resistance of gray iron castings to atmospheric corrosion and to corrosion in some ant to atmospheric andacid corrosion than gray iron, so that improved resistance is obtained by surfacing gray iron castings with a chill. The effect of the chilled surface was determined as follows: Specimens 1 inch x '3 inches x 1; inch of gray iron whose surfaces were and were not chilled by tellurium were totally immersed in 2 per cent sulfuric acid and 2 per cent hydrochloric acid for-26 hours, the acids being renewed every 1 hours. Weight losses in grams in these two acids after immersion were:
' Surface treatment H 80 2% RC1 None 4. 16 5. 51 With tellurium 3. 08 2. 29
Similar irons, with and without chilled surfaces, when exposed to the weather for a year lost 0.37 gram and 0.61 gram per square inch of surface, respectively, showing that a marked decrease in corrosion loss obtains as a result of providing the castings with chilled surfaces.
Our invention of utilizing tellurium and tellurium-bearing materials to provide chilled surfaces and localized chilled areas on gray iron castings is suitable for a wide range-of applications. Articles such as cams on cast iron camshafts, teeth on cast iron gears, various castings on agricultural equipment, cast iron paving blocks, sections of cast iron roofing, and other cast iron articles requiring resistance to wear, abrasion, or corrosion are examples where our invention is applicable.
It is to be understood that when the term tellurium is used in the following claims, alloys of tellurium and compounds and other materials containing tellurium are also included.
Having thus described our invention, what we claim is:
1. A method of forming chilled surfaces on a gray iron casting which comprises applying tellurium to the surface of a mold cavity and then pouring the iron into such mold cavity, the tellurium being applied to the surface of the mold cavity, in an amount suflicient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent.
2. A method of forming chilled surfaces on a gray iron casting comprising the application of a mold wash containing tellurium to-the surface of a mold cavity and then pouring the iron therein, the mold wash containing tellurium in an amount sufficient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent. V
3. A method of forming chilled surfaces on a gray iron casting which comprises the application of from 0.005 gram to 0.3 gram of tellurium to each square inch of surface of a mold cavity and then pouring the iron therein.
4. A method of forming localized chilled surface areas on a gray iron casting, said method comprising the coating of the surface of the mold cavity with tellurium at such locations corresponding to the areas of localized chill on the casting, then pouring the iron therein, the tellurium being applied to the surface of the mold cavity in an amount sufiicient to produce a chilled iron layer adjacent the surface of the casting characterized by the presence of tellurium in an amount ranging from 0.001 to 0.5 per cent.
5. A wear-resistant cast iron article comprising a layer oi! chilled iron on a gray iron casting, said chilledironlayer being characterized by the presence 01' tellurium in an amount ranging irom 0.001 per cent to 0.5 per cent.
6. As a new article of manufacture, a cast iron the basic composition or which without a-tellurium content would normally be from gray to mottled if cast without chilling, said cast iron having a hard wear-resistant surface and containing tellurium in eflective amount in said surtacecaullngit tobehardandwhiteand greater in percentage as compared with the interior of the same.
'l. A method of forming chilled surfaces on a gray iron casting which comprises applying tellurium to the surface of a mold cavity and then pouring the iron into such mold cavity. the tcllurium being applied to the surface of the mold cavity in an amount aumcient to produce a chilled iron layer adjacent the surface oi the casting. 4
CLARENCE H. LORIG. DANIEL E. KRAUBE.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US223322A US2250488A (en) | 1938-08-05 | 1938-08-05 | Cast iron and a method of producing chilled surfaces thereon |
US367264A US2250489A (en) | 1938-08-05 | 1940-11-26 | Method of producing chilled surfaces on cast iron |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US223322A US2250488A (en) | 1938-08-05 | 1938-08-05 | Cast iron and a method of producing chilled surfaces thereon |
Publications (1)
Publication Number | Publication Date |
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US2250488A true US2250488A (en) | 1941-07-29 |
Family
ID=22836012
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US223322A Expired - Lifetime US2250488A (en) | 1938-08-05 | 1938-08-05 | Cast iron and a method of producing chilled surfaces thereon |
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US (1) | US2250488A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2450395A (en) * | 1944-08-02 | 1948-09-28 | Crane Co | Malleable cast iron |
US2979793A (en) * | 1958-05-08 | 1961-04-18 | American Brake Shoe Co | Cast iron |
US3228766A (en) * | 1965-02-01 | 1966-01-11 | Inland Steel Co | Method for adding tellurium to steel |
US3235394A (en) * | 1961-10-03 | 1966-02-15 | Foseco Int | Mold dressing composition |
US3411957A (en) * | 1965-06-01 | 1968-11-19 | Nisso Seiko Kabushiki Kaisha | Method of manufacturing a cast iron roll |
US4003425A (en) * | 1975-02-11 | 1977-01-18 | The British Cast Iron Research Assoc. | Method of and means for obtaining white cast iron |
US4029140A (en) * | 1975-04-01 | 1977-06-14 | The British Cast Iron Research Association | Method of and means for obtaining white cast iron |
US4059996A (en) * | 1975-11-20 | 1977-11-29 | Electro-Nite Co. | Molten metal sample cup containing blob for promoting carbide formation |
EP0010513A1 (en) * | 1978-10-09 | 1980-04-30 | Mitsubishi Jukogyo Kabushiki Kaisha | Process for producing spherical graphite castings |
US5316068A (en) * | 1989-01-20 | 1994-05-31 | Aisin Seiki Kabushiki Kaisha | Method for producing casting with functional gradient |
US5337800A (en) * | 1992-09-09 | 1994-08-16 | Cook Arnold J | Reactive coating |
US5615730A (en) * | 1993-10-15 | 1997-04-01 | Nippon Sublance Probe Engineering Ltd. | Methods for inspecting the content of structure modifying additives in molten cast iron and chilling tendency of flaky graphite cast iron |
-
1938
- 1938-08-05 US US223322A patent/US2250488A/en not_active Expired - Lifetime
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2450395A (en) * | 1944-08-02 | 1948-09-28 | Crane Co | Malleable cast iron |
US2979793A (en) * | 1958-05-08 | 1961-04-18 | American Brake Shoe Co | Cast iron |
US3235394A (en) * | 1961-10-03 | 1966-02-15 | Foseco Int | Mold dressing composition |
US3228766A (en) * | 1965-02-01 | 1966-01-11 | Inland Steel Co | Method for adding tellurium to steel |
US3411957A (en) * | 1965-06-01 | 1968-11-19 | Nisso Seiko Kabushiki Kaisha | Method of manufacturing a cast iron roll |
US4003425A (en) * | 1975-02-11 | 1977-01-18 | The British Cast Iron Research Assoc. | Method of and means for obtaining white cast iron |
US4029140A (en) * | 1975-04-01 | 1977-06-14 | The British Cast Iron Research Association | Method of and means for obtaining white cast iron |
US4059996A (en) * | 1975-11-20 | 1977-11-29 | Electro-Nite Co. | Molten metal sample cup containing blob for promoting carbide formation |
EP0010513A1 (en) * | 1978-10-09 | 1980-04-30 | Mitsubishi Jukogyo Kabushiki Kaisha | Process for producing spherical graphite castings |
US5316068A (en) * | 1989-01-20 | 1994-05-31 | Aisin Seiki Kabushiki Kaisha | Method for producing casting with functional gradient |
US5337800A (en) * | 1992-09-09 | 1994-08-16 | Cook Arnold J | Reactive coating |
US5615730A (en) * | 1993-10-15 | 1997-04-01 | Nippon Sublance Probe Engineering Ltd. | Methods for inspecting the content of structure modifying additives in molten cast iron and chilling tendency of flaky graphite cast iron |
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