US1358810A - Process of treating magnetizable material - Google Patents
Process of treating magnetizable material Download PDFInfo
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- US1358810A US1358810A US287593A US28759319A US1358810A US 1358810 A US1358810 A US 1358810A US 287593 A US287593 A US 287593A US 28759319 A US28759319 A US 28759319A US 1358810 A US1358810 A US 1358810A
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- 239000000463 material Substances 0.000 title description 30
- 238000000034 method Methods 0.000 title description 27
- 230000008569 process Effects 0.000 title description 16
- 229910052799 carbon Inorganic materials 0.000 description 41
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 40
- 229910045601 alloy Inorganic materials 0.000 description 30
- 239000000956 alloy Substances 0.000 description 30
- 230000001590 oxidative effect Effects 0.000 description 24
- 238000000137 annealing Methods 0.000 description 22
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 21
- 239000012535 impurity Substances 0.000 description 15
- 238000001816 cooling Methods 0.000 description 14
- 230000035699 permeability Effects 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 13
- 229910000976 Electrical steel Inorganic materials 0.000 description 10
- 229910000640 Fe alloy Inorganic materials 0.000 description 10
- 229910052742 iron Inorganic materials 0.000 description 10
- 239000007789 gas Substances 0.000 description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 230000004927 fusion Effects 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 5
- 229910052753 mercury Inorganic materials 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000007769 metal material Substances 0.000 description 3
- 238000005096 rolling process Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 229910000676 Si alloy Inorganic materials 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000005764 Theobroma cacao ssp. cacao Nutrition 0.000 description 2
- 235000005767 Theobroma cacao ssp. sphaerocarpum Nutrition 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 235000001046 cacaotero Nutrition 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- XWHPIFXRKKHEKR-UHFFFAOYSA-N iron silicon Chemical compound [Si].[Fe] XWHPIFXRKKHEKR-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 238000010583 slow cooling Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 241001446467 Mama Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- ANTSCNMPPGJYLG-UHFFFAOYSA-N chlordiazepoxide Chemical compound O=N=1CC(NC)=NC2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 ANTSCNMPPGJYLG-UHFFFAOYSA-N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical compound [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/12—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
- C21D8/1244—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
- C21D8/1255—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest with diffusion of elements, e.g. decarburising, nitriding
-
- 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
- C21D3/00—Diffusion processes for extraction of non-metals; Furnaces therefor
- C21D3/02—Extraction of non-metals
- C21D3/04—Decarburising
Definitions
- My invention relates to magnetizable materials in general and more particularly to iron and to magnetizable alloys of iron with silicon or aluminum, and of iron with silicon and aluminum, and it has, for its object, a method of improving 'the magnetic qualities, character. ,7
- alloys containing only small amounts of impurlties, at 950 C. for one hour, in a current'of air, with the pressure in the furnace reduced to about 2 millimeters ofv mercury and have then cooled them, to room temperature, at the rate of about 30 0. per hour, resulting in a doubling or tripling of the maximum permeability.
- the reduced pressure is not essential, as similar results have been obtained by annealing at atmospheric pressure.
- test pieces from the same steel annealed at the same temperature under other conditions such as in a vacuum, ina current of hydrogen, or a current of nitrogen, under a pressure of 2 millimeters of mercury, gave a maximum permeability of less than 10,000 and a hysteresis loss of more than It is therefore, evident that the improvement is due to removal of some oxidizable impurity or impurities, the oxids of which are removable as a gas.
- the carbon removed from the steel by practising my invention in the above instance corresponded to about 0.10% of the weight of the test pieces calculated from the amount ofCO and CO gases given on during the treatment. As this amount corresponded very closely to the original carbon content of the alloy, as determined by chemical analysis, it is believed that the improvements noted are chiefly occasioned by the removal of carbon.
- the carbon content of iron can be reduced to 0.01%, or lower, by subjecting the molten iron to the action of a vacuum in the presence of a small amount been formed on orin the librium is established.
- reaction (1) evidently takes place until the carbon content is very low, perhaps less than 0.01%, while the reaction (2) does not commence until the carbon is eliminated, or very nearly so. If the oxidization is carried beyond the point at which the carbon. is eliminated, a decrease in permeability and an increase in hysteresis loss takes place.
- l/Vhile iron and iron alloys may be materially improved, as regards their magnetic qualities, by annealing them under oxidizpointed out, to carry the oxidization to such extent'as to, in part, counteract the advantages obtained.
- the temperatime to which the metal is annealed and the rate of flow of the oxidizing gas, if an oxidizing gas is used, so accurately as to obtain the best results I prefer, in many cases, to carry the annealing, under oxidizing conditions, slightly to excess and to then subject the metal to reducing conditions to restore it to its desired state.
- I may first treat the alloy of iron and silicon, or an equivalent alloy, under oxidizing conditions, in the manner previouslydescribed, to such extent that the impurities, especially carbon, the oxids of which are carried off as gases, are definitely known to have been decreased to the desired amount. This may be done even at the risk of oxidizing the material itself to some extent.
- the material may be subjected to a reducmg condition in order to reduce the oxid or oxids that may have material.
- a reducmg condition in order to reduce the oxid or oxids that may have material.
- any suitable reducing agent may be employed that will not r'e-introduce impurities into the material.
- a current of hydrogen has been used to good effect.
- a sample of 4% ironsilicon alloy was annealed at 1100 (1., under slightly oxidizing conditions, with the result that its maximum permeability was raised to 37,500.
- the sample was then reannealed at 1100 C. under a more intense oxidizing condition that resulted, after slow ing conditions, it is possible, as previously cooling, in adecrease of the maximum permeability to 27,000. 1
- the same sample was then annealed at 1100 G., in a current of hydrogen, with the result that the permeability .Was increased to 32,000.
- a second treatment of hydrogen not only did not increase the permeability but actually decreased it to 23,300 showing that the hydro gen treatment should not be carried on in-
- the process embodied in my present invention is applicable to the material in all forms, such as rods, bars, sheets and the like, by regulating the elements of time, temperature and rate of flow of the oxidizing gas. This regulation is, however, very diflicult if the material comprises large stacks of very thin sheets of the iron, or iron alloy, and, consequently, non-uniformity of the product is apt to result.
- I may take material in the form of sheet-bars, say six inches by twentyfour inches by one-half inch thickness, and treat it under oxidizing conditions to such extent that the impurities are reduced to a sufiiciently low amount to give the material the improved magnetic qualities desired. If the time, temperature and the like required for the treatment have been determined by test runs, the usual slow cooling of the treated material may be omitted, at this point, and the sheet-bars may be removed from the furnace, freed from scale in any convenient manner, and rolled. down to sheets of the desired thickness.
- the refined silicon steel, or other material is much more ductile than before the treatment and may tures than would otherwise be required.
- the sheets After the material has been rolled into sheets, the sheets must be annealed at a sufficiently high temperature800 to l100 C.to eliminate the effect of the mechanical treatment, after which they are slowly cooled to ordinary temperature. This reannealing must be carried on under such conditions that the material shall not be contaminated by either carbon or oxygen. This maybe done by any suitable means, as the be moreeasily rolled at lower temperaprovision of a neutral or slightly reducing atmosphere, or the initial annealing under ox dlzing conditions may be discontinued shortly before all of the removable. impurities have been eliminated, under which condit1on,the remaining impurities will be removed during the re-annealing and will thus keep the material from absorbing oxygen or carbon.
- the material may initially anneal or heat the material, under oxidizing conditions, until it is slightly silicon steel in the form of a three-eighths.
- inch sheet-bar was annealed at 900 (3., in cacao, and slowlycooled. It then had a maximum permeability of about 5,000 and Y a hysteresis loss of about 1,950 ergs per cubic centimeter, per cycle. After annealing the sample in accordance with my present .invention under oxidizing conditions, at 900 C. and at reduced pressure, until the carbon was substantially eliminated, and slowly cooling it, itsmaximum permeability was over 30,000 and its hysteresis loss was less than 600 ergs.
- the sheet-bar was then forged and rolled into thin sheets, varying from 14 to 125 .mils, which were annealed Mama, at 900 to 1100 (l, to counteract the effect of the rolling.
- the maximum per% meability of these sheets was then found to be between 17,000 and 30,000 and the hy steresis loss was from 450 to 650 ergs.
- the same sheet-bar, if rolled directly down to sheets of the above thicknesses would, after annealing in vacuo, have a maximum permeability of only 5000 to 6000 and ahysteresis 7 loss as great as 1,400 to 1,600 ergs.
- the dizing conditions has been carried so far as to slightly oxidize the alloy, the latter may be re-annealed, under'reducing conditions, and then slowly cooled. Also, after the annealing under oxidizing conditions, or after the annealing under reducing conditions, if
- annealing after the mechanical -treatment, to keep the material from absorbing oxygen or carbon during such'final annealing or the final annealing may be done in a neutral or slightly reducing atmosphere.
- each weighing 1600 grams and formed of 4% silicon steel containing 0.1% carbon were employed.
- the several samples were annealed at 900, 950, 1000 and 1050 (3., respectively, in a current of air of 120 cubic centimeters per minute and at a pressure of 2 millimeters of mercury. Under these conditions, to bring the maximum permeability of the samples above 30,000, it was necessary to anneal the sample at 1050 for thirteen-hours, the sample at 100Q for twenty hours, that at 950 for one hundred hours and that at 900 for two hundred hours. It is, therefore, distinctly advantageous to employ the higher temperatures, even if doing so involves more furnace difficulties than arise with the lower temperatures.
- the amounts of carbon eliminated from the several samples were substantially the same.
- the relationship between the maximum permeability-or hysteresis loss-and the carbon remaining is so constant that the amount of carbon removed may be utilized as an indicator of the progress made in the treatment of the material.
- the total carbon co tent of the steel to e treated from'prev'ous chemical analysisgthe curve betwe en the time required and the carbon to be eliminated may be determined and the treatment may be continued accordingly until the carbon content has been reduced to the desired amount. For the best results this should be less than 0.01%.
- I of carbon during the annealin process is the chieffactor in improving t e' magnetic. qualities of the alloys, it is very probable that other impurities are also eliminated to a greater or'less degree.
- silicon steel has been annealed' at temperatures between 1100 and 1325 (1., preferably the latter, under a requisite low pressure, not to exceed/2.5 millim'eters of mercury, or in a' reducing atmosphere, to remove some of its impurities, particularly the oxygen, and to thus reduce its hysteresis loss as much as A patent to William E. Ruder, No. 1,110,010, dated.
- the method of improving the magnetic qualities of a magnetizable metallic material which comprises heating the material at relatively high temperature, but short of fusion, to remove certain impurities, particularly carbon and then cooling it.
- the method of improving the magnetic qualities of magnetizable alloys such as alloys of iron with silicon, or taluminum, or both which comprises heating the allo at relatively high temperature, but short 0 fusion, under oxidizing conditions until substantially all carbon present has been eliminated and then slowl cooling it.
- the method 0 improving magnetic qualities of a magnetizable iron alloy which comprises heating the alloy at a relatively high temperature, but short of fusion, under oxidizing conditions, further heating the alloy at a relatively high temperature, but short of fusion, under slightly reducing conditions and then slowly cooling it.
- the method of improving the magnetic qualities of a magnetizable alloy which comprises heating the alloy at a temperature between 800 and 1100 C. and under slightly oxidizing conditions until all or substantiall all of the carbon has been eliminated, furt er heating'the alloy under slightly reducin conditions and then slowly cooling forging the alloy to the desired form -ana. nealing the alloy and then slowlycooling the alloy.
- the method of treatin a nag netiz able iron alloy which comprises eating the alloy under oxidizing conditions to remove substantially all of its contained carbon, heating the alloy under slightly reducing conditions, to remove any oxids formed by the previous heating, mechanically treating the alloy to suitably form it, annealing the formed alloy to counteract the efiects of the mechanical treatment and slowly cooling the annealed alloy.
- the method of treating a magnetic alloy which comprises heating the alloy under oxidizing conditions to remove substantially all of its carbon content, forging and rolling the alloy to sheet form, annealing the alloy to eliminate the efiect of the mechanical treatment, the annealing being done under conditions preventing absorption of carbon and oxygen and slowly cooling the an nealed alloy.
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- Thermal Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Electromagnetism (AREA)
- Mechanical Engineering (AREA)
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Description
UNITED STA'lilflS ATENT OFFICE.
' TRYGVE n. YENSEN, oF'swIssvALn, PENNSYLVANIA, ASSIG-NOR 'ro WESTIlN'GHOUSE ELECTRIC & MA UFACTURING COMPANY, A CORPORATION OF PENNSYLVANIA.
PBOCESS OF TREATING MAGNETIZABLE MATERIAL.
No Drawing.
To all whom it may concern -Be it known that I, TRYGVE D YnNsnN,
a citizen of the United States, and a resident of Swissvale, in the county of Alle- Processes of Treatin 'Magnetizable Material, of which the f lowingis a specification.
My invention relates to magnetizable materials in general and more particularly to iron and to magnetizable alloys of iron with silicon or aluminum, and of iron with silicon and aluminum, and it has, for its object, a method of improving 'the magnetic qualities, character. ,7
As disclosed in my Patent No. 1,277,523, dated'Sept. 3, 1918, I have found that the magnetic properties of iron and iron alloys are very much improved by reducing their contained impurities, especiallycarbon, below the amounts ordinarily found in the best grades of present commercial products. The process there set forth consists essentially in melting and treating the iron, or
or properties, of alloys of such iron alloys, in 'vacuo, to substantially remove or eliminate, the impurities, originally present, particularly carbon. By practising the above-referred-to invention, I have obtained magnetizable materials that have magnetic permeabilities even five times higher and hysteresis losses only one fifth as high as those of the best materials previously known. I
On account of the expense involved in practising, the process just referred to, it became very desirable to find some, other and cheaper method whereby the same results could be obtained.
I have now found that it is possible to purify alloys,.such as I have referred to, in their solid state and to thus improve their magnetic qualities very materially. My present invention comprehends the treatment of magnetizable alloys, in solidstate, in the form of sheets, rods, bars and the like,
and essentially comprises subjecting the alloys to oxidizing conditions, at relatively high temperatures, followed by slow cooling, the process being performed at atmos- Specification of Letters Patent. I
1,000 ergs.
Patented Nov. 16, 1920.
Application filed April 4, 1919. Serial No. 287,593.-
alloys, containing only small amounts of impurlties, at 950 C. for one hour, in a current'of air, with the pressure in the furnace reduced to about 2 millimeters ofv mercury and have then cooled them, to room temperature, at the rate of about 30 0. per hour, resulting in a doubling or tripling of the maximum permeability. The reduced pressure is not essential, as similar results have been obtained by annealing at atmospheric pressure.
Of ccurse the higher the percentage'of impuritles present and the greater the crosssection of the pieces being treated, the longer the heat treatment must be continued. On the other hand, the higher the temperature employed, the more rapidly the diffusion of the impurities to the surface will take place and the shorter will be the'time necessary for the treatment.
By practising my present invention on commercial 4% silicon steel, containing up to 0.1% carbon I have, for example, been able to obtain a product having a maximum permeability of over 40,000 and a hysteresis loss of less than 250 ergs per cubic centimeter per cycle for B:10,000. In comparison, test pieces from the same steel annealed at the same temperature under other conditions, such as in a vacuum, ina current of hydrogen, or a current of nitrogen, under a pressure of 2 millimeters of mercury, gave a maximum permeability of less than 10,000 and a hysteresis loss of more than It is therefore, evident that the improvement is due to removal of some oxidizable impurity or impurities, the oxids of which are removable as a gas.
The carbon removed from the steel by practising my invention in the above instance corresponded to about 0.10% of the weight of the test pieces calculated from the amount ofCO and CO gases given on during the treatment. As this amount corresponded very closely to the original carbon content of the alloy, as determined by chemical analysis, it is believed that the improvements noted are chiefly occasioned by the removal of carbon.
As has been pointed out in my previouslyreferred-to patent, the carbon content of iron can be reduced to 0.01%, or lower, by subjecting the molten iron to the action of a vacuum in the presence of a small amount been formed on orin the librium is established. The resultsobtained in iron-silicon alloys show that this reaction also takes place in the presence of silicon, in preference to the reaction (2) Si+2FeO=SiO +Fe In the case of solid materials, at temperature above 900 (1., both the carbon and silicon are in solid solution in the iron and, in the presence of oxide or oxygen, reaction (1) evidently takes place until the carbon content is very low, perhaps less than 0.01%, while the reaction (2) does not commence until the carbon is eliminated, or very nearly so. If the oxidization is carried beyond the point at which the carbon. is eliminated, a decrease in permeability and an increase in hysteresis loss takes place.
l/Vhile iron and iron alloys may be materially improved, as regards their magnetic qualities, by annealing them under oxidizpointed out, to carry the oxidization to such extent'as to, in part, counteract the advantages obtained. As it is difficult to regulate the duration of the treatment, the temperatime to which the metal is annealed and the rate of flow of the oxidizing gas, if an oxidizing gas is used, so accurately as to obtain the best results, I prefer, in many cases, to carry the annealing, under oxidizing conditions, slightly to excess and to then subject the metal to reducing conditions to restore it to its desired state.
For example, in practising my invention, I may first treat the alloy of iron and silicon, or an equivalent alloy, under oxidizing conditions, in the manner previouslydescribed, to such extent that the impurities, especially carbon, the oxids of which are carried off as gases, are definitely known to have been decreased to the desired amount. This may be done even at the risk of oxidizing the material itself to some extent.
ollowing this step,-the material may be subjected to a reducmg condition in order to reduce the oxid or oxids that may have material. For this purpose, any suitable reducing agent may be employed that will not r'e-introduce impurities into the material. For example, in practice, a current of hydrogen has been used to good effect.
In one instance, a sample of 4% ironsilicon alloy was annealed at 1100 (1., under slightly oxidizing conditions, with the result that its maximum permeability was raised to 37,500. The sample was then reannealed at 1100 C. under a more intense oxidizing condition that resulted, after slow ing conditions, it is possible, as previously cooling, in adecrease of the maximum permeability to 27,000. 1 The same sample was then annealed at 1100 G., in a current of hydrogen, with the result that the permeability .Was increased to 32,000. A second treatment of hydrogen not only did not increase the permeability but actually decreased it to 23,300 showing that the hydro gen treatment should not be carried on in- The process embodied in my present invention is applicable to the material in all forms, such as rods, bars, sheets and the like, by regulating the elements of time, temperature and rate of flow of the oxidizing gas. This regulation is, however, very diflicult if the material comprises large stacks of very thin sheets of the iron, or iron alloy, and, consequently, non-uniformity of the product is apt to result.
I have found that this difficulty may be overcome :by treating the material, in the form of bars, to remove the impurities, particularly carbon, rolling the treated bars down into sheets .of the desired thickness and then annealing the sheets to eliminate the effects of the mechanical treatment. 7
F or example, I may take material in the form of sheet-bars, say six inches by twentyfour inches by one-half inch thickness, and treat it under oxidizing conditions to such extent that the impurities are reduced to a sufiiciently low amount to give the material the improved magnetic qualities desired. If the time, temperature and the like required for the treatment have been determined by test runs, the usual slow cooling of the treated material may be omitted, at this point, and the sheet-bars may be removed from the furnace, freed from scale in any convenient manner, and rolled. down to sheets of the desired thickness. The refined silicon steel, or other material, is much more ductile than before the treatment and may tures than would otherwise be required.
After the material has been rolled into sheets, the sheets must be annealed at a sufficiently high temperature800 to l100 C.to eliminate the effect of the mechanical treatment, after which they are slowly cooled to ordinary temperature. This reannealing must be carried on under such conditions that the material shall not be contaminated by either carbon or oxygen. This maybe done by any suitable means, as the be moreeasily rolled at lower temperaprovision of a neutral or slightly reducing atmosphere, or the initial annealing under ox dlzing conditions may be discontinued shortly before all of the removable. impurities have been eliminated, under which condit1on,the remaining impurities will be removed during the re-annealing and will thus keep the material from absorbing oxygen or carbon.
In place of the foregoing operations, I
may initially anneal or heat the material, under oxidizing conditions, until it is slightly silicon steel in the form of a three-eighths.
inch sheet-bar was annealed at 900 (3., in cacao, and slowlycooled. It then had a maximum permeability of about 5,000 and Y a hysteresis loss of about 1,950 ergs per cubic centimeter, per cycle. After annealing the sample in accordance with my present .invention under oxidizing conditions, at 900 C. and at reduced pressure, until the carbon was substantially eliminated, and slowly cooling it, itsmaximum permeability was over 30,000 and its hysteresis loss was less than 600 ergs. The sheet-bar was then forged and rolled into thin sheets, varying from 14 to 125 .mils, which were annealed Mama, at 900 to 1100 (l, to counteract the effect of the rolling. The maximum per% meability of these sheets was then found to be between 17,000 and 30,000 and the hy steresis loss was from 450 to 650 ergs. The same sheet-bar, if rolled directly down to sheets of the above thicknesses would, after annealing in vacuo, have a maximum permeability of only 5000 to 6000 and ahysteresis 7 loss as great as 1,400 to 1,600 ergs.
' dizing conditions, either with or without reducing the pressure, and then slowly cooling it".
While the two steps of annealing and cooling are the essential features of my process, certain other operations may be performed before the final step of cooling, if desired.
For example, if the annealing under oxi.-
dizing conditions has been carried so far as to slightly oxidize the alloy, the latter may be re-annealed, under'reducing conditions, and then slowly cooled. Also, after the annealing under oxidizing conditions, or after the annealing under reducing conditions, if
such annealing is employed, the material the annealing, under oxidizing conditions,
may be shortened slightly so that slight impurities will remain to be removed by the final. annealing, after the mechanical -treatment, to keep the material from absorbing oxygen or carbon during such'final annealing or the final annealing may be done in a neutral or slightly reducing atmosphere.
While I have described my process as comprising subjecting'the material to oxidizing conditions, I wish'it understood that the term includes the treatment of the material with some oxid, as iron oxid, such as annealing it surrounded by, and in contact with, the oxid, as well as in a current ofsome oxidizing gas.
The time required, at the various temperatures which may be employed in practising my invention, may be illustrated by the following examples. Samples, in the form of bars three-eighths' of an inch thick,
each weighing 1600 grams and formed of 4% silicon steel containing 0.1% carbon were employed. The several samples were annealed at 900, 950, 1000 and 1050 (3., respectively, in a current of air of 120 cubic centimeters per minute and at a pressure of 2 millimeters of mercury. Under these conditions, to bring the maximum permeability of the samples above 30,000, it was necessary to anneal the sample at 1050 for thirteen-hours, the sample at 100Q for twenty hours, that at 950 for one hundred hours and that at 900 for two hundred hours. It is, therefore, distinctly advantageous to employ the higher temperatures, even if doing so involves more furnace difficulties than arise with the lower temperatures. The amounts of carbon eliminated from the several samples were substantially the same.
As a matter of fact, the relationship between the maximum permeability-or hysteresis loss-and the carbon remaining is so constant that the amount of carbon removed may be utilized as an indicator of the progress made in the treatment of the material. Knowin the total carbon co tent of the steel to e treated, from'prev'ous chemical analysisgthe curve betwe en the time required and the carbon to be eliminated may be determined and the treatment may be continued accordingly until the carbon content has been reduced to the desired amount. For the best results this should be less than 0.01%. Although I of carbon during the annealin process is the chieffactor in improving t e' magnetic. qualities of the alloys, it is very probable that other impurities are also eliminated to a greater or'less degree. However, as yet, I have no definite evidence to this effect but I do know that annealing iron, or iron alloys,under oxidizing conditions,,for certain lengths of time and at thetemperatures believe that the elimination specified, reduces the carboncontent to perhaps less than 0.01% and remarkably improves the magnetic permeability and hysteresis loss.
The presence of even a few hundredths of a per cent. of carbon in silicon steel may produce 100% increase in the hysteresis loss over that of carbon-free alloy and I have found that even up to 0.05% carbon will remain even if the alloy is melted and kept under a pressure of 2 millimeters of mercury unless there is enough oxid present to oxidize the carbon, which is rarely the case with silicon steel.
I am aware that silicon steel has been annealed' at temperatures between 1100 and 1325 (1., preferably the latter, under a requisite low pressure, not to exceed/2.5 millim'eters of mercury, or in a' reducing atmosphere, to remove some of its impurities, particularly the oxygen, and to thus reduce its hysteresis loss as much as A patent to William E. Ruder, No. 1,110,010, dated.
Sept. 8, 1914, covers such a method and attributes its effectiveness to the reduction of.
oxids and to the fact that by it the normal grains of silicon steel are coalesced into a lesser number of larger grains.
I have taken the product resulting from the Ruder process with its 30% decreased hysteresis loss, treated it in accordance with my present invention, and thereby reduced its previously reduced hysteresis loss by 50% and even'75%.
This clearly indicates the distinction between the Ruder process, which is essen- .t1ally one of reductlon, and my process ducedto as low as 0.001%.
nearly all, of this carbon.
' which is primarily one of oxidization. As
even melting a silicon steel in cacao will leave in it a residue of as much as 0.05% carbon, it appears that the Ruder process would leave at least that much carbon present and I ascribe the marked decrease in hysteresis loss, achieved by my process, as occasioned by the elimination of all, or
In other words, by my process, which is essentially one of oxidization, I remove a remarkable proportion of the carbon. Because of the difficulty of accurate analysis, the ultimate limit of carbon removal by my process is not definitely known but I believe that, by prolonged treatment, it may be re- However, analysis of the CO gas given off from the furnace during the treatment would indicate that the marked improvement in the magnetic qualities of 4% silicon steel takes place over the decrease from 0.03% to 0.01% of carbon.
As I have not only described the essential features of my invention but have also set "fortha number of added operations, which may be performed at the will of any one practising my invention, or to suit various conditions and requirements, no restrictions which comprises heating the material at a relatively high temperature, but short of fusion, under oxidizing conditions and then slowly cooling it.
2. The method of improving the magnetic qualities of a magnetizable metallic material which comprises heating the material at relatively high temperature, but short of fusion, to remove certain impurities, particularly carbon and then cooling it.
3. The method of improving the magnetic qualities of a magnetizable metallic material which comprises heating the material at a temperature between 800 and 1100 C. to remove substantially all of the carbon and then cooling it. I j
4. The method of improving the magnetic qualities of a magnetizable metallic material which comprises heating the material under slightly oxidizing conditions until substantially-all the carbon has been removed and then cooling it at. the rate of substantially 30 C. per hour.
5. The method of improving the magnetic qualities of magnetizable alloys such as alloys of iron with silicon, or taluminum, or both which comprises heating the allo at relatively high temperature, but short 0 fusion, under oxidizing conditions until substantially all carbon present has been eliminated and then slowl cooling it.
6. The method 0 improving magnetic qualities of a magnetizable iron alloy which comprises heating the alloy at a relatively high temperature, but short of fusion, under oxidizing conditions, further heating the alloy at a relatively high temperature, but short of fusion, under slightly reducing conditions and then slowly cooling it.
7. The method of improving the magnetic qualities of a magnetizable alloy which comprises heating the alloy at a temperature between 800 and 1100 C. and under slightly oxidizing conditions until all or substantiall all of the carbon has been eliminated, furt er heating'the alloy under slightly reducin conditions and then slowly cooling forging the alloy to the desired form -ana. nealing the alloy and then slowlycooling the alloy.
9. The method of treatin a nag netiz able iron alloy which comprises eating the alloy under oxidizing conditions to remove substantially all of its contained carbon, heating the alloy under slightly reducing conditions, to remove any oxids formed by the previous heating, mechanically treating the alloy to suitably form it, annealing the formed alloy to counteract the efiects of the mechanical treatment and slowly cooling the annealed alloy.
10. The method of treating a magnetic alloy which comprises heating the alloy under oxidizing conditions to remove substantially all of its carbon content, forging and rolling the alloy to sheet form, annealing the alloy to eliminate the efiect of the mechanical treatment, the annealing being done under conditions preventing absorption of carbon and oxygen and slowly cooling the an nealed alloy.
In testimony whereof, I have hereunto subscribed my name this 25th day of March, 1919.
TRYGVE n. YENSEN.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US287593A US1358810A (en) | 1919-04-04 | 1919-04-04 | Process of treating magnetizable material |
FR512966A FR512966A (en) | 1919-04-04 | 1920-04-03 | Magnetizable materials treatment process |
GB9651/20A GB141348A (en) | 1919-04-04 | 1920-04-06 | Process of improving the magnetic qualities of magnetizable material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US287593A US1358810A (en) | 1919-04-04 | 1919-04-04 | Process of treating magnetizable material |
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US1358810A true US1358810A (en) | 1920-11-16 |
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US287593A Expired - Lifetime US1358810A (en) | 1919-04-04 | 1919-04-04 | Process of treating magnetizable material |
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US (1) | US1358810A (en) |
FR (1) | FR512966A (en) |
GB (1) | GB141348A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2442762A (en) * | 1943-09-09 | 1948-06-08 | Bell Telephone Labor Inc | Methods of improving the magnetic quality of anisotropic permanent magnets containing iron, nickel, cobalt, and aluminum |
US2875113A (en) * | 1957-11-15 | 1959-02-24 | Gen Electric | Method of decarburizing silicon steel in a wet inert gas atmosphere |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2270762A (en) * | 1939-01-31 | 1942-01-20 | Gen Electric | Cold rolled silicon steel strip |
-
1919
- 1919-04-04 US US287593A patent/US1358810A/en not_active Expired - Lifetime
-
1920
- 1920-04-03 FR FR512966A patent/FR512966A/en not_active Expired
- 1920-04-06 GB GB9651/20A patent/GB141348A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2442762A (en) * | 1943-09-09 | 1948-06-08 | Bell Telephone Labor Inc | Methods of improving the magnetic quality of anisotropic permanent magnets containing iron, nickel, cobalt, and aluminum |
US2875113A (en) * | 1957-11-15 | 1959-02-24 | Gen Electric | Method of decarburizing silicon steel in a wet inert gas atmosphere |
Also Published As
Publication number | Publication date |
---|---|
FR512966A (en) | 1921-02-04 |
GB141348A (en) | 1921-01-20 |
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