US2711979A - Process of cutting stainless steel and the like - Google Patents
Process of cutting stainless steel and the like Download PDFInfo
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- US2711979A US2711979A US294083A US29408352A US2711979A US 2711979 A US2711979 A US 2711979A US 294083 A US294083 A US 294083A US 29408352 A US29408352 A US 29408352A US 2711979 A US2711979 A US 2711979A
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- 238000005520 cutting process Methods 0.000 title claims description 34
- 238000000034 method Methods 0.000 title claims description 18
- 229910001220 stainless steel Inorganic materials 0.000 title claims description 12
- 239000010935 stainless steel Substances 0.000 title description 6
- 230000008569 process Effects 0.000 title description 4
- 229910052751 metal Inorganic materials 0.000 claims description 48
- 239000002184 metal Substances 0.000 claims description 48
- 239000000203 mixture Substances 0.000 claims description 41
- 239000001257 hydrogen Substances 0.000 claims description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims description 33
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 22
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 16
- 239000001301 oxygen Substances 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 150000002739 metals Chemical class 0.000 claims description 15
- 230000009471 action Effects 0.000 claims description 10
- 230000015572 biosynthetic process Effects 0.000 claims description 7
- 230000006872 improvement Effects 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 28
- 239000007789 gas Substances 0.000 description 27
- 239000012159 carrier gas Substances 0.000 description 22
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- 239000001569 carbon dioxide Substances 0.000 description 10
- 229910002092 carbon dioxide Inorganic materials 0.000 description 10
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229910052786 argon Inorganic materials 0.000 description 6
- 239000001307 helium Substances 0.000 description 6
- 229910052734 helium Inorganic materials 0.000 description 6
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 6
- 230000001590 oxidative effect Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 4
- 239000000956 alloy Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000001464 adherent effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000012254 powdered material Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910000616 Ferromanganese Inorganic materials 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XTCJSAMDLIVJCP-UHFFFAOYSA-N aluminum;manganese Chemical compound [Al+3].[Mn].[Mn].[Mn] XTCJSAMDLIVJCP-UHFFFAOYSA-N 0.000 description 1
- 239000001996 bearing alloy Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000003292 diminished effect Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 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
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K7/00—Cutting, scarfing, or desurfacing by applying flames
- B23K7/08—Cutting, scarfing, or desurfacing by applying flames by applying additional compounds or means favouring the cutting, scarfing, or desurfacing procedure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/228—Selection of materials for cutting
Definitions
- This invention relates to improvementsin cutting of metal bodies, such as stainless steel and the like, which can not be effectively cut by conventional flame cutting procedures. Specifically, the invention provides an improvement in the metal surface resulting from the cut by eliminating or reducing scale that is otherwise formed and which adheres tightly to such surfaces.
- Typical of the metals normally immune or resistant to ordinary flame cutting are the austenitic stainless steels, such as those containing approximately 18% chromium and 8% nickel or manganese, as well as other chromium-bearing alloy steels, and
- the flux-forming materials that may be thus employed I are, in general, those whichvare themselves oxidized or burned in oxygen with the generation of intense-heat, and the action of the flux-forming material to make possible flame cutting of the metals named may be due to the fact that the material burns to produce much higher 1 temperatures than would be attained in its absence, or may be due to the combination of the oxidation products of the flux-forming material with those of the metal body being cut to produce an easily removable slag, or the action may be due, in part, to both of these effects.
- the flux-forming materials useful for the purpose just described preferably are metals or alloys in powdered form.
- One of the most effective flux-forming "materials is finely divided, substantially pure, iron powder having a particle size such that all of it will pass through 100 mesh screen and most of it will pass thrOughlSO-ZOO mesh screen.
- Other metal powders useful for this purpose include powdered aluminum; manganese; ferromanganese alloys, such as those containing about 80% manganese; and mixtures of iron with any of these in various-proportions.
- 'n'on'metallic materials such as sodium carbonate
- these are most effective if they are modified by admixture with iron powder or" with onc"'of-'the other metallic powder-s mentioned above.
- l j I Various ways have been proposed fol-delivering the flux-forming powder to the part to be cut. This has been done both with and without a carrier gas for the powdered material, Where a carrier gas for the powdered material has been used, it has been proposed to employ the stream of cutting oxygen (or a portion of it), the combustible gas mixture that is burned to preheat the It is known that these metals can be cut by the ice metal to be cut, or a separate stream of another gas, such as compressed air or nitrogen.
- This scale has been found to be formed onthe cut metal surface under virtually all conditions, regardless of the particular flux-forming powder employed and regardless of the method by which the powder was delivered to the cut.
- the principal object is to affect the total metal treated, or at least, large areas, for refining grain structure or the like, whereas in flame cutting, the desideratum sought is not to affect, or to affect as little as possible, the metal other than the exact location of the cut. Therefore, it is apparent that both the degree and the extent of heating and their purposes are radically different in the heat treating art as compared to flame-cutting of metals.
- the principal object of the present invention is to improve the metal surface resulting from the cutting action of a stream of oxygen and a flux-forming material applied concurrently to the preheated metal, and particularly to reduce or to prevent the formation of tightly adhering scale on the cut metal surface. Additionally, the present invention makes possible a method in which such scale as may be formed upon the cut metal surface is of a dilferent character from that heretofore encountered, and may be easily removed. Other objects will hereinafter appear.
- the resultant cu't metal-surfaces thus obtained arefound to be substantially free of tightly adherent scale, and such scale as may be present on these surfaces is loose and may be easily removed. This is an important advantage in precision shape cutting of stainless steel and the like, especially where the cut surface of the metal must be cleaned in advance of subsequent operations employing the out part.
- the non infiammablemixtures in air of' thenon-oxidizing gas and hydrogen used in the practice of. this invention must contain at least by volume of hydrogen; I prefer to use between about and about by volume of hydrogen in the carrier gas with optimum results being attained at about 20% byvolume of hydrogen.
- the maximum amount of hydrogen that can be safely used has been determined to be about 38% by volume.
- the remainder of the carrier gas may be any gas of the group named above.
- Nitrogen alone when used as a carrier gas. for the flux-forming materials does not enable the desired effect of scale prevention or the formation of a loose scale to be attained, and no other single gas of the group named is practically effective for this purpose.
- Mixtures of hydrogen with any one of the gases named in the specified proportions are, however, extremely effective.
- the upper limit of hydrogen in admixture with the non-oxidizing gases for the purpose of this invention is around 38% by volume. This represents the dilution limit of infiammability in air of the preferred mixtures of hydrogen with nitrogen, and is, in effect, a border-line composition for this mixture of gases. Any increase, even as little as 1% or 2% by volume, in the hydrogen content, renders the mixture inflammable in air. Furthermore, a higher hydrogen content necessarily increases the cost of the mixture, in addition to increasing the hazards involved in its use.
- the upper limit of hydrogen in admixture with carbon dioxide representing the dilution limit of inflammability in air was about 37% by volume.
- nitrogen-hydrogen mixtures it was found that at least 5% by volume of hydrogen must be used with carbon dioxide.
- the preferred range for use with carbon dioxide is between about 10% and about 20% by volume of hydrogen in the carrier gas, and optimum resultswere obtained with mixtures of about 23% by volume of hydrogen and 77% by volume of carbon dioxide.
- the improvements in the condition of the metal surfaces using this latter gas mixture compare favorably with those obtained through the use of a mixture of 20% hydrogen with 80% nitrogen by volume as the carrier gas.
- Argon and helium in admixture with hydrogen in the proportions previously set forth are also effective for the purposes of this invention, but the relatively higher cost of such gases as argon and helium probably would preclude Loss in H2;-
- the gas mixtures containing hydrogen employed in I accordance with this invention may. be and preferably are premixed in advance of their use. However, it is possible to-produce at least certain of the desired gases in situ, for example, by the decomposition of ammonia which will occur in the flame.
- a gasv consisting principally of nitrogen (or other suitablev nonoxidizing gas) and containing sufiicient ammonia to result, on decomposition of the latter, in a mixture; as, described above may be used, and it will be understood that reference to mixtures of, hydrogen, with non-oxidizing gases in the appended claims includes chemically producedmixtures as well as those made by combining the gases as such.
- the improvement comprising the step of delivering the fluxforming material to the site of the cut in a stream of a carrier gas comprising a mixture of a gas which is non oxidizing under said specific flame cutting conditions, with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air, thereby improving the metal surface by reducing or preventing the formation of tightly adhering scale.
- the improvement comprising the step of delivering the fluxforming material to the site of the cut in a stream of a carrier gas comprising a mixture of a gas of the group consisting of nitrogen, carbon dioxide, argon and helium with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air, thereby improving the metal surface by reducing or preventing the formation of tightly adhering scale.
- the carrier gas consists of a mixture of nitrogen with about 5% to 37% by volume of hydrogen.
- the carrier gas consists of a mixture of carbon dioxide with about 5% to about 37% by volume of hydrogen.
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- Arc Welding In General (AREA)
Description
United States Patent PROCESS OF CUTTING STAINLESS STEEL AND THE LIKE John B. La Pota, Chicago, 111., assignor to National Cylinder Gas Company, Chicago, 111., a corporation of Delaware No Drawing. Application June 17, 1952, Serial No, 294,083
8 Claims. (Cl. 148-9) This invention relates to improvementsin cutting of metal bodies, such as stainless steel and the like, which can not be effectively cut by conventional flame cutting procedures. Specifically, the invention provides an improvement in the metal surface resulting from the cut by eliminating or reducing scale that is otherwise formed and which adheres tightly to such surfaces.
Many metal bodies are difficult or almost impossible to cut by the ordinaryflame cutting procedures in which a stream or jet of oxygen is directed against a preheated portion of the metal. .Typical of the metals normally immune or resistant to ordinary flame cutting are the austenitic stainless steels, such as those containing approximately 18% chromium and 8% nickel or manganese, as well as other chromium-bearing alloy steels, and
the nickel base alloys, such as those containing princi- The flux-forming materials that may be thus employed I are, in general, those whichvare themselves oxidized or burned in oxygen with the generation of intense-heat, and the action of the flux-forming material to make possible flame cutting of the metals named may be due to the fact that the material burns to produce much higher 1 temperatures than would be attained in its absence, or may be due to the combination of the oxidation products of the flux-forming material with those of the metal body being cut to produce an easily removable slag, or the action may be due, in part, to both of these effects.
. The flux-forming materials useful for the purpose just described preferably are metals or alloys in powdered form. One of the most effective flux-forming "materials is finely divided, substantially pure, iron powder having a particle size such that all of it will pass through 100 mesh screen and most of it will pass thrOughlSO-ZOO mesh screen. Other metal powders useful for this purpose include powdered aluminum; manganese; ferromanganese alloys, such as those containing about 80% manganese; and mixtures of iron with any of these in various-proportions. In some cases, 'n'on'metallic materials, such as sodium carbonate, may be used; and these are most effective if they are modified by admixture with iron powder or" with onc"'of-'the other metallic powder-s mentioned above. l j I Various ways have been proposed fol-delivering the flux-forming powder to the part to be cut. This has been done both with and without a carrier gas for the powdered material, Where a carrier gas for the powdered material has been used, it has been proposed to employ the stream of cutting oxygen (or a portion of it), the combustible gas mixture that is burned to preheat the It is known that these metals can be cut by the ice metal to be cut, or a separate stream of another gas, such as compressed air or nitrogen.
Suitable apparatus for carrying out cutting operations employing a flux-forming powdered material as described above, and in which this material is supplied to the site of the cut by means of a separate carrier gas, is shown in Chouinard & LaPota co-pending application, Serial No. 749,412, filed May 21, 1947, now Patent No. 2,657,650,
granted November 3, 1953, and in LaPota co-pending.
application, Serial No. 758,736, filed July 3, 1947, now Patent No. 2,608,446, granted August 26, 1952.
The surface of a metal body, such as stainless steel, that has been formed by flame cutting employing the methods outlined above, ordinarily is found to be covered with a tightly adhering scale that is very difficult to remove. This scale has been found to be formed onthe cut metal surface under virtually all conditions, regardless of the particular flux-forming powder employed and regardless of the method by which the powder was delivered to the cut.
Protective atmospheres consisting of hydrogen alone, nitrogen alone and mixtures of these gases are known in the related but non-analogous art of heat treating metals, where they are employed to prevent scale formation due, primarily, to oxidation. These gases serve their purpose chiefly by replacing air in contact with the metals being treated, and this normally requires a suitable enclosure for the entire work. In the art of flame-cutting metals however, high pressure oxygen is directed upon the work and the maintenance of an artificial atmosphere is impractical, and one that is oxygen free is impossible. Also, in heat treating of metals, the principal object is to affect the total metal treated, or at least, large areas, for refining grain structure or the like, whereas in flame cutting, the desideratum sought is not to affect, or to affect as little as possible, the metal other than the exact location of the cut. Therefore, it is apparent that both the degree and the extent of heating and their purposes are radically different in the heat treating art as compared to flame-cutting of metals. I
Accordingly, the principal object of the present invention is to improve the metal surface resulting from the cutting action of a stream of oxygen and a flux-forming material applied concurrently to the preheated metal, and particularly to reduce or to prevent the formation of tightly adhering scale on the cut metal surface. Additionally, the present invention makes possible a method in which such scale as may be formed upon the cut metal surface is of a dilferent character from that heretofore encountered, and may be easily removed. Other objects will hereinafter appear.
I have discovered that these objects may be attained, and that improved flame cutting of metal bodies ordinarily resistant or immune to conventional flame cutting may be carried out by the aid of a flux-forming powder delivered to the site of the cut in a carrier gas which is composed of a mixture of a gas which is non-oxidizing under the above referred to'flame cutting conditions with an effective amountofhydrogen, and in which mixture the proportions'of the gases are such as to result in a composition that is non-inflammable in air. -The gases defined and contemplated as being non-oxidizing under the particular flame cutting conditions here involved include nitrogen, carbon dioxide, argon and helium. The resultant cu't metal-surfaces thus obtained arefound to be substantially free of tightly adherent scale, and such scale as may be present on these surfaces is loose and may be easily removed. This is an important advantage in precision shape cutting of stainless steel and the like, especially where the cut surface of the metal must be cleaned in advance of subsequent operations employing the out part.
'l'ests have demonstrated that to be effective for practicalpurposes, the non infiammablemixtures in air of' thenon-oxidizing gas and hydrogen used in the practice of. this invention must contain at least by volume of hydrogen; I prefer to use between about and about by volume of hydrogen in the carrier gas with optimum results being attained at about 20% byvolume of hydrogen. The maximum amount of hydrogen that can be safely used has been determined to be about 38% by volume. The remainder of the carrier gas may be any gas of the group named above.
Mixtures of nitrogen with hydrogen are preferred as a matter of convenience and economy, although as statedabove; helium, argon or carbon dioxide may be substituted for the nitrogen. Nitrogen alone when used as a carrier gas. for the flux-forming materials does not enable the desired effect of scale prevention or the formation of a loose scale to be attained, and no other single gas of the group named is practically effective for this purpose. Mixtures of hydrogen with any one of the gases named in the specified proportions are, however, extremely effective.
Metallurgical studies of the heat-affected zone and of the metal surfaces resulting from cuts made in austenitic stainless steels using the carrier gas mixtures of this invention have shown distinct ancillary advantages. Specifically, the heat-affected zone is less than is the case when carrier gases proposed prior to this invention are used, and within this reduced heat-affected zone there is a further reduction in the proportion of it within which undesirable grain growth occurs. These improvements most probably are achieved because the less dense and non-adherent scale formed in the practice of this invention admit of a more rapid cooling of the cut surfaces and contiguous areas through the critical range. Moreover, the physical properties of the metal cut are not materially impaired nor are its corrosion-resistant properties diminished. While these metallurgical benefits are obtained through the use of any of the carrier gas mixtures within the scope of my invention as described above, they are most pronounced and the maximum advantages in all of the respects set forth are obtained through the employment of the preferred carrier gas composed of mixtures of nitrogen with from 5% to 38% by volume of hydrogen.
The upper limit of hydrogen in admixture with the non-oxidizing gases for the purpose of this invention, as stated above, is around 38% by volume. This represents the dilution limit of infiammability in air of the preferred mixtures of hydrogen with nitrogen, and is, in effect, a border-line composition for this mixture of gases. Any increase, even as little as 1% or 2% by volume, in the hydrogen content, renders the mixture inflammable in air. Furthermore, a higher hydrogen content necessarily increases the cost of the mixture, in addition to increasing the hazards involved in its use.
In tests conducted with hydrogen-carbon dioxide mixtures, the upper limit of hydrogen in admixture with carbon dioxide representing the dilution limit of inflammability in air was about 37% by volume. As was the case with nitrogen-hydrogen mixtures, it was found that at least 5% by volume of hydrogen must be used with carbon dioxide. Also, the preferred range for use with carbon dioxide is between about 10% and about 20% by volume of hydrogen in the carrier gas, and optimum resultswere obtained with mixtures of about 23% by volume of hydrogen and 77% by volume of carbon dioxide. The improvements in the condition of the metal surfaces using this latter gas mixture compare favorably with those obtained through the use of a mixture of 20% hydrogen with 80% nitrogen by volume as the carrier gas.
Argon and helium in admixture with hydrogen in the proportions previously set forth are also effective for the purposes of this invention, but the relatively higher cost of such gases as argon and helium probably would preclude Loss in H2;-
\ Mesh size:
them from all but special uses, and for this reason, dct-ailed discussion of such mixtures is omitted here.
The action by which this invention prevents or reduces the formation of tightly adhering scale on cut metal surfaces cannot be stated exactly. It seems probable that the gases, particularly the hydrogen, are absorbed on or dissolved in the molten metal as the cut is made and thereafter areexpelled beneath; the scale-forming surface when the molten metal solidifies and cools, with the result that the action. inI eliminating, scale or preventing it reaches the point at which its ignition isd'esiredinthecutting operation. In any event, the use of the mixtures of gases specified above as a carrier gas to conveythe flux-forming materials supplied to facilitate cutting of metal bodies normally immune or highly resistant to convcntional flame cutting makes possible a distinct improvement in the quality of the cut metal surface.
The highest quality of cuts made in austenitic stainless steels of the so-call'ed 18 and 8' types have been found to result from the use of a flux-forming material composed essentially of pure iron powder delivered to the site of the cut in a carrier gas composed of a dry, oxygen-free mixture of 80% nitrogen with 20% hydrogen. The specific composition and particle size of a preferred iron powder for obtaining cuts of the best quality is asfollows:
Chemical analysisv Element; Percent by weight 99188 0.008 0.019 0.006 0.006 0.002 0.004 0.09 Apparent density 2.60-2.70
Screen analysis Percent by weight On 80; None On Trace On 200 15-20 On 325 15-25 Through 325 60-70 By the use of this combination of flux-forming materials and carrier gas in accordance with my invention, shape cutting of stainless steel can be conducted with high efficiency and a minimum of metal is consumed since the kerf produced by the cut is very clean and narrow. The cut metal surfaces are substantially free from tightly adherent scale and may be easily prepared for further use or fabrication.
The gas mixtures containing hydrogen employed in I accordance with this invention may. be and preferably are premixed in advance of their use. However, it is possible to-produce at least certain of the desired gases in situ, for example, by the decomposition of ammonia which will occur in the flame. In this case,. a gasv consisting principally of nitrogen (or other suitablev nonoxidizing gas) and containing sufiicient ammonia to result, on decomposition of the latter, in a mixture; as, described above may be used, and it will be understood that reference to mixtures of, hydrogen, with non-oxidizing gases in the appended claims includes chemically producedmixtures as well as those made by combining the gases as such.
Other modifications and variations of details of the invention will be apparent to those skilled in this art, and these are also included in its scope as defined by th: appended claims.
This application is a continuation-in-part of and is substituted for my co-pending application Serial No. 154,894, filed April 8, 1950, now abandoned, which, in turn, was a continuation-in-part of my application Serial No. 752,289, filed June 3, 1947, and now abandoned.
I claim:
1. In the method. of cutting metals normally immune or resistant to conventional flame cutting with preheat and oxygen alone, such as stainless steels and the like, by the action of a flux-forming material applied concurrently with a stream of oxygen to the preheated metal, the improvement comprising the step of delivering the fluxforming material to the site of the cut in a stream of a carrier gas comprising a mixture of a gas which is non oxidizing under said specific flame cutting conditions, with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air, thereby improving the metal surface by reducing or preventing the formation of tightly adhering scale.
2. In the method of cutting metals normally immune or resistant to conventional flame cutting with preheat and oxygen alone, such as stainless steels and the like, by the action of a flux-forming material applied concurrently with a stream of oxygen to the preheated metal, the improvement comprising the step of delivering the fluxforming material to the site of the cut in a stream of a carrier gas comprising a mixture of a gas of the group consisting of nitrogen, carbon dioxide, argon and helium with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air, thereby improving the metal surface by reducing or preventing the formation of tightly adhering scale.
3. The method of claim 2, in which the mixture contains from about 5% to about 37% by volume of hydro gen.
4. The method of claim 2, in which the mixture contains from about to about 20% by volume of hydrogen.
5. The method of claim 2, in which the carrier gas consists of a mixture of nitrogen with about 5% to 37% by volume of hydrogen.
6. The method of claim 2, in which the carrier gas consists of a mixture of carbon dioxide with about 5% to about 37% by volume of hydrogen.
7. Method of improving the metallurgical properties of the cut surfaces and adajcent areas, of metals normally immune or resistant to conventional flame cutting with preheat and oxygen alone, in the process of cutting them by the action of a flux-forming material applied concurrently with a stream of oxygen to the preheated metal, by reducing the heat affected zone and further reducing the portion within said heat affected zone Within which undesirable grain growth occurs, comprising the step of delivering the flux-forming material to the site of the cut in a stream of carrier gas consisting of a mixture of a gas which is non-oxidizing under said specific flame cutting conditions, admixed with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air.
8. Method of improving the metallurgical properties of the cut surfaces and adjacent areas, of metals normally immune or resistant to conventional flame cutting with preheat and oxygen alone, in the process of cutting them by the action of a flux-forming material applied concurrently with a stream of oxygen to the preheated metal, by reducing the heat affected zone and further reducing the portion within said heat affected zone with which undesirable grain growth occurs, comprising the step of delivering the flux-forming material to the site of the cut in a stream of carrier gas comprising a gas from the group consisting of nitrogen, carbon dioxide, argon and helium admixed with at least 5% by volume of hydrogen and not more than will render the mixture inflammable in air.
References Cited in the file of this patent UNITED STATES PATENTS 1,924,136 Stern Aug. 29, 1933 2,286,192 Aitchison et a1 June 16, 1942 2,491,440 Boedecker et a1 Dec. 13, 1949 OTHER REFERENCES Slowter et al., Treatise in Metals and Alloys, Feb. 1938, page 34 (complete article pages 33-39 inclusive).
Claims (1)
1. IN THE METHOD OF CUTTING METALS NORMALLY IMMUNE OR RESISTANT TO CONVENTIONAL FLAME CUTTING WITH PREHEAT AND OXYGEN ALONE, SUCH AS STAINLESS STEELS AND THE LIKE, BY THE ACTION OF A FLUX-FORMING MATERIAL APPLIED CONCURENTLY WITH A STREAM OF OXYGEN TO THE PREHEATED METAL, THE IMPROVEMENT COMPRISING THE STEPS OF DELIVERING THE FLUXFORMING MATERIAL TO THE SITE OF THE CUT IN A STREAM OF A CARRIER GAS COMPRISING A MIXTURE OF A GAS WHICH IS NOOXIDIZING UNDER SAID SPECIFIC FLAME CUTTING CONDITIONS, WITH AT LEAST 5% BY VOLUME OF HYDROGEN AND NOT MORE THAN WILL RENDER THE MIXTURE INFLAMMABLE IN AIR, THEREBY IMPROVING THE METAL SURFACE BY REDUCING OR PREVENTING THE FORMATION OF TIGHTLY ADHERING SCALE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US294083A US2711979A (en) | 1952-06-17 | 1952-06-17 | Process of cutting stainless steel and the like |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US294083A US2711979A (en) | 1952-06-17 | 1952-06-17 | Process of cutting stainless steel and the like |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2711979A true US2711979A (en) | 1955-06-28 |
Family
ID=23131809
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US294083A Expired - Lifetime US2711979A (en) | 1952-06-17 | 1952-06-17 | Process of cutting stainless steel and the like |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2711979A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034874A (en) * | 1955-03-07 | 1962-05-15 | Reynolds Metals Co | Blow torch fuel and method of burning same |
| US3447879A (en) * | 1967-11-06 | 1969-06-03 | Aeroprojects Inc | Cutting torch and method for achieving high temperature cutting |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1924136A (en) * | 1931-04-02 | 1933-08-29 | Barrett Co | Process for heating materials |
| US2286192A (en) * | 1939-04-18 | 1942-06-16 | Linde Air Prod Co | Mineral piercing and cutting |
| US2491440A (en) * | 1947-02-05 | 1949-12-13 | Bastian Blessing Co | Apparatus for flame-cutting metal |
-
1952
- 1952-06-17 US US294083A patent/US2711979A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1924136A (en) * | 1931-04-02 | 1933-08-29 | Barrett Co | Process for heating materials |
| US2286192A (en) * | 1939-04-18 | 1942-06-16 | Linde Air Prod Co | Mineral piercing and cutting |
| US2491440A (en) * | 1947-02-05 | 1949-12-13 | Bastian Blessing Co | Apparatus for flame-cutting metal |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3034874A (en) * | 1955-03-07 | 1962-05-15 | Reynolds Metals Co | Blow torch fuel and method of burning same |
| US3447879A (en) * | 1967-11-06 | 1969-06-03 | Aeroprojects Inc | Cutting torch and method for achieving high temperature cutting |
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