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US3178324A - Method of producing ultrafine grained steel - Google Patents

Method of producing ultrafine grained steel Download PDF

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US3178324A
US3178324A US285121A US28512163A US3178324A US 3178324 A US3178324 A US 3178324A US 285121 A US285121 A US 285121A US 28512163 A US28512163 A US 28512163A US 3178324 A US3178324 A US 3178324A
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steel
heating
grain
austenite
grain size
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US285121A
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Raymond A Grange
Edward R Shackelford
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United States Steel Corp
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    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D1/00General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
    • C21D1/78Combined heat-treatments not provided for above
    • C21D1/785Thermocycling

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  • fine grain size in steel has long been recognized because of its effect on the strength, ductility and other mechanical properties of steel.
  • fine grain has only been obtainable by steel production techniques such as by deoxidizing with silicon and aluminum or the addition of grain refining elements such as vanadium or columbium.
  • Steels containing aluminum, vanadium, columbiurn and other grain refining elements in sufficient amounts to refine the grains are fine grained and resist grain coarsening in that they can be heated well above the Ac temperature for considerable time.
  • the use of such elements adds to the expense of the steels and particularly in the case of aluminum results in a killed steel so that hot topping practice is required.
  • Another object is to produce an ultrafine grained condition in steel by heat treatment following forging or rolling the steel to the desired shape or gauge.
  • an ultrafine grain size can be produced in steel by a multicycle heat treatment consisting of rapidly heating the steel in less than 60 seconds to a temperature above the AC1 to convert ferrite to austenite but below the temperature at which austenite grains coarsen rapidly and as soon thereafter as possible cooling it before the austenite grains so formed can grow appreciably.
  • the cooling in all but the last cycle must be sufficiently fast to develop a structure of the class consisting of bainite, martensite or mixtures thereof and thus avoid transformation to a ferrite-pearlite microstructure.
  • air cooling which develops a ferritepearlite microstructure, may be used if desired.
  • the steel is not heated more than 150 F. above its Ac temperature.
  • the steels suitable for grain refinement by this process are all those which are hardenable by heat treatment, are predominantly ferritic rather than austenitic at room temperature, and become completely austenitic on heating to a suitable elevated temperature. This excludes only highalloy steels such as austenitic or ferritic stainless steels.
  • steels responsive to our process consist of martensite or of carbides in a matrix of ferrite. When heated into the critical range, ferrite begins to transform into austenite by a nucleation and growth process.
  • Ferrite grain boundaries are preferred nucleation sites for austenite, and furthermore there is a strong tendency for austenite once nucleated to grow until it has consumed the particular ferrite grain in which it nucleated and then to cease growing for a time.
  • austenite grains assume the shape and size of the prior ferrite grains. However, this is only a temporary situation because growth of the austenite grains is also occurring, by which process more stable grains consume adjacent less stable grains. If the heating rate is relatively fast, the austenite grain growth process is slower than the ferrite to austenite transformation.
  • the heating be done quite rapidly but once the desired rate is obtained on further advantage results from exceeding such rate by extremely fast heating.
  • satisfactory results can be obtained by leadbath heating but other types of liquid baths, such as salts, or electrical induction or resistance heating may be used.
  • the heating time should be less than 60 seconds and preferably less than 20 seconds. In such thicknesses as .03 to .50 inch, the same ultrafine grain size was obtained upon heating in a lead bath from 10 to 20 seconds.
  • the treatment may involve cooling to room temperature after austenitiz-ing, it is only essential to cool sufficiently to insure transformation of the austenite to bainite, martensite or mixtures thereof and avoid the formation of ferrite-pearlite on all cycles except possibly the last.
  • the cooling may be done in any convenient manner but must be sufficiently rapid to minimize austenite grain growth at temperatures above the critical range. Thus for thin sections air quenching will suffice but heavier sections will require water or other liquid quenching.
  • the steel should be cooled at a rate which develops the desired metallographic structure for the intended use of the product. No additional heat treatment other than subcritical term savanna 3 pering or annealing should be used thereafter because the ultrafine grain achieved by the treatment may be wholly or partially lost.
  • the single figure of the drawing illustrates schematically a four-cycle treatment showing the degree of grain refinement obtained by one, two and four cycles in comparison with the hot rolled structure.
  • the steel used in obtaining the data for the figure was SAE 1045 which had been hot rolled to 0.150-inch-thick. strip. Heating was accomplished by immersing in a lead bath maintained at 1500 F. for 20 seconds. The A temperature of this steel is 1420 F. As shown, an ultrafine grain size of #11 ASTM was obtained in two cycles, with slightly finer grain resulting from two additional cycles. No appreciable improvement was obtained by additional cycles beyond the four shown.
  • the specimens were oil quenched after the first cycle of the two-cycle specimen and after the first, second and third cycle of the four-cycle specimen. The final cooling in each case was air cooling.
  • Table I gives data obtained from treating representative hypoeutectoid steels in accordance with the invention. This table compares the grain size obtained by one, two, and four cycles with that obtained by the indicated conventional austenitizing treatment.
  • the medium carbon steels often developed the full improvement in grain size with two cycles but the low carbon steels required more than two cycles to do so.
  • the difficulty in developing full grain refinement in low carbon steels is believed to result from their higher Ac; temperature whereby they must be heated to higher temperatures to austenitize them.
  • the optimum heating temperature and time may vary with steel composition but generally the optimum temperature will be about the same as that conventionally used for austenitizing each steel. While the maximum grain refinement is generally obtained y in two to four cycles, further cycles may in some cases be required particularly with hypereutectoid steels wherein the dispersion of small undissolved carbide particles developed minimizes grain growth.
  • Table III shows that the type of deoxidation has little, if any, effect on the grain size obtained by practicing the invention.
  • steel produced by coarse-grain practice i.e., silicon-killed had the same fine grain size #14 ASTM after four cycles as a steel produced to fine grain practice, i.e., killed with silicon and alumi- 3U num.
  • steels treated in accordance with this invention have better toughness, ductility and yield strength than conventionally heat treated steels.
  • a method of producing ultrafine grain size in steel which is predominately ferritic rather than austenitic at room temperature, becomes completely austenitic on heating to suitable elevated temperature and thereafter becomes ferritic on cooling to room temperature comprising cyclically treating such steel by heating it at least twice to above its A0 temperature but below the temperature at which austenite grains coarsen rapidly for just sufiicient time to transform it to an austenitic structure and then before any appreciable grain growth occurs quickly cooling it to transform the austenite in all but the last cycle to a microstructure of the class consisting of martensite, bainite or mixtures thereof and in the last cycle cooling at a rate which will produce the desired microstructure whereby an austenite grain size finer than ASTM is produced therein.
  • a method of producing ultrafine grain size in steel which is predominately ferritic rather than austenitic at room temperature, becomes completely austenitic on heating to suitable elevated temperature and thereafter becomes ferritic on cooling to room temperature comprising cyclically treating such steel by heating it at least twice in less than seconds to above its Ac temperature but References Cited by the Examiner UNITED STATES PATENTS 1,919,983 7/33 Morrill 148-144 OTHER REFERENCES Principles of Heat Treatment by M. A. Grossmann, published by the A.S.M. (1935), page 203 relied upon.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Description

April 13, 1965 R. A. GRANGE ETAL METHOD OF PRODUCING ULTRAFINE GRAINED STEEL Filed June 5. 1963 4 Th. CYCLE 3 Rd. C YCL E s1. 2 CYCLE CYCLE Sec.
5. 89 .5 av 3 52m ROOM TEMP ma MEE EEQ ASTM No. 12
TIME 2 crcu:
ASTM No. II
ASTM N0. 10
INITIAL srRucTl (HOT IIPOLLED) ASTM No. 5
INVENTORS. RAYMOND A. GRANGE and EDWARD R. .S'HACKELFORD Attorn United States Patent Ofitice Patented Apr. 13, 1965 3,178,324 METHOD OF PRDDUCTNG ULTRAFENE GRAINED TEEL Raymond A. Grange, Washington Township, Westmoreland County, Pa, and Edward R. Shacirelford, Chicago, Ill., assignors to United States Steel Corporation, a corporation of New Jersey Filed June 3, 1963, Ser. No. 285,121 2 Claims. (Cl. 148-143) This invention relates to the production of ultrafine grained steel and more particularly to the production of ultrafine grain size in steel by heat treatment.
The desirability of fine grain size in steel has long been recognized because of its effect on the strength, ductility and other mechanical properties of steel. Heretofore fine grain has only been obtainable by steel production techniques such as by deoxidizing with silicon and aluminum or the addition of grain refining elements such as vanadium or columbium. Steels containing aluminum, vanadium, columbiurn and other grain refining elements in sufficient amounts to refine the grains are fine grained and resist grain coarsening in that they can be heated well above the Ac temperature for considerable time. However, the use of such elements adds to the expense of the steels and particularly in the case of aluminum results in a killed steel so that hot topping practice is required. Moreover the obtaining of fine grain in such manner precludes the obtainin of a relatively pure rim portion such as results from a full rimming action. Applicants have discovered that it is possible to produce even finer grains than is conventionally obtained with deoxidizing or grain refining elements by suitable heat treatment alone. The fine grain so produced is finer than #10 on the ASTM grain size chart and may accordingly be termed ultrafine grained.
Thus it is an object of the present invention to obviate the necessity of using deoxidizing or grain refining elements in the production of fine grained steels.
Another object is to produce an ultrafine grained condition in steel by heat treatment following forging or rolling the steel to the desired shape or gauge.
The foregoing and further objects will be apparent from the following specification when read in conjunction with the attached drawing illustrating the teaching of the invention as applied to SAE 1045 steel.
We have discovered that an ultrafine grain size can be produced in steel by a multicycle heat treatment consisting of rapidly heating the steel in less than 60 seconds to a temperature above the AC1 to convert ferrite to austenite but below the temperature at which austenite grains coarsen rapidly and as soon thereafter as possible cooling it before the austenite grains so formed can grow appreciably. The cooling in all but the last cycle must be sufficiently fast to develop a structure of the class consisting of bainite, martensite or mixtures thereof and thus avoid transformation to a ferrite-pearlite microstructure. In the last cycle, air cooling, which develops a ferritepearlite microstructure, may be used if desired. Preferably the steel is not heated more than 150 F. above its Ac temperature. In some steels two such cycles will produce substantially the finest grains possible although in others continued refinement may result by repeating the cycle three or more times. The optimum number of cycles varies among steels of different compositions depending primarily upon the nature of the initial and intermediate metallographic structures developed by cooling after each cycle.
The steels suitable for grain refinement by this process are all those which are hardenable by heat treatment, are predominantly ferritic rather than austenitic at room temperature, and become completely austenitic on heating to a suitable elevated temperature. This excludes only highalloy steels such as austenitic or ferritic stainless steels. At room temperature, steels responsive to our process consist of martensite or of carbides in a matrix of ferrite. When heated into the critical range, ferrite begins to transform into austenite by a nucleation and growth process. Ferrite grain boundaries are preferred nucleation sites for austenite, and furthermore there is a strong tendency for austenite once nucleated to grow until it has consumed the particular ferrite grain in which it nucleated and then to cease growing for a time. Thus, as steel is heated into its critical range, austenite grains assume the shape and size of the prior ferrite grains. However, this is only a temporary situation because growth of the austenite grains is also occurring, by which process more stable grains consume adjacent less stable grains. If the heating rate is relatively fast, the austenite grain growth process is slower than the ferrite to austenite transformation. This makes it possible to retain in the final product an austenite grain size closely related to the prior ferrite grain size by rapidly heating to a temperature just sufficiently above the critical range to austenitize the steel .and then cooling immediately. The resulting ferrite grain size is smaller than the parent austenite grain size. Thus, heating rapidly so as to expose austenite to temperatures above the critical range for a time barely snfficient to convert all ferrite to austenite and cooling quickly results in refinement of grain size. Furthermore, repeating this short heating cycle produces additional grain refinement because at the start of the second cycle the ferrite grain size is smaller than at the start of the first cycle. Thus, mulicycle rapid heating leads to progressive grain refinement. After a certain number of cycles, depending on the particular steel and specific heating cycle, no additional grain refinement is produced, however, because growth occurs more and more rapidly as austenite grains are made ever finer on successive heating cycles until eventually a stalemate is reached.
It requires at least two cycles to obtain the maximum grain refinement and about four cycles will almost always develop the maximum refinement. The number of cycles to produce such result varies depending primarily upon steel composition and upon the nature of the initial and intermediate metallographic structures developed by cooling after each cycle.
In practicing our invention, it is necessary that the heating be done quite rapidly but once the desired rate is obtained on further advantage results from exceeding such rate by extremely fast heating. In thicknesses up to 0.5 inch, satisfactory results can be obtained by leadbath heating but other types of liquid baths, such as salts, or electrical induction or resistance heating may be used. The heating time should be less than 60 seconds and preferably less than 20 seconds. In such thicknesses as .03 to .50 inch, the same ultrafine grain size was obtained upon heating in a lead bath from 10 to 20 seconds.
While the treatment may involve cooling to room temperature after austenitiz-ing, it is only essential to cool sufficiently to insure transformation of the austenite to bainite, martensite or mixtures thereof and avoid the formation of ferrite-pearlite on all cycles except possibly the last. The cooling may be done in any convenient manner but must be sufficiently rapid to minimize austenite grain growth at temperatures above the critical range. Thus for thin sections air quenching will suffice but heavier sections will require water or other liquid quenching. After the final heating cycle, the steel should be cooled at a rate which develops the desired metallographic structure for the intended use of the product. No additional heat treatment other than subcritical term savanna 3 pering or annealing should be used thereafter because the ultrafine grain achieved by the treatment may be wholly or partially lost.
The single figure of the drawing illustrates schematically a four-cycle treatment showing the degree of grain refinement obtained by one, two and four cycles in comparison with the hot rolled structure. The steel used in obtaining the data for the figure was SAE 1045 which had been hot rolled to 0.150-inch-thick. strip. Heating was accomplished by immersing in a lead bath maintained at 1500 F. for 20 seconds. The A temperature of this steel is 1420 F. As shown, an ultrafine grain size of #11 ASTM was obtained in two cycles, with slightly finer grain resulting from two additional cycles. No appreciable improvement was obtained by additional cycles beyond the four shown. In the cyclic treatment of FIGURE 1, the specimens were oil quenched after the first cycle of the two-cycle specimen and after the first, second and third cycle of the four-cycle specimen. The final cooling in each case was air cooling.
The following Table I gives data obtained from treating representative hypoeutectoid steels in accordance with the invention. This table compares the grain size obtained by one, two, and four cycles with that obtained by the indicated conventional austenitizing treatment. The medium carbon steels often developed the full improvement in grain size with two cycles but the low carbon steels required more than two cycles to do so. The difficulty in developing full grain refinement in low carbon steels is believed to result from their higher Ac; temperature whereby they must be heated to higher temperatures to austenitize them.
1 Heated in air for 20 minutes at 1,550 F. (except 1,600" F. for 1015 and The following Table 11 gives data obtained from treating high carbon steels pursuant to the invention. If such steels are heated sufiiciently high to dissolve all the carultrafine grain size.
TABLE 11 Grain refinement in hypereutectoid steels Austenitc grain size, ASTM N0. Heating Grade tcmp., SAE No. Undis- 1 cycle 2 cycles 4 cycles solved l0 carbides 1085 1, 550 10% 11 None.
1, 500 11 11% 12 Trace. 1, 450 y 16 Many. 4360 1, 550 10% 13% 13% Few.
1, 500 10 14 16 h lany. 10 438i) l, 500 10 14% 17 11111113 1 Heated for 10 seconds in lead. N01E.Spcci1ncns were 0.100-inch-thick strip.
0 As indicated heremabove the optimum heating temperature and time may vary with steel composition but generally the optimum temperature will be about the same as that conventionally used for austenitizing each steel. While the maximum grain refinement is generally obtained y in two to four cycles, further cycles may in some cases be required particularly with hypereutectoid steels wherein the dispersion of small undissolved carbide particles developed minimizes grain growth.
The following Table III shows that the type of deoxidation has little, if any, effect on the grain size obtained by practicing the invention. Thus in the case of 0.1-inchthick specimens of l045 steels tested, steel produced by coarse-grain practice, i.e., silicon-killed had the same fine grain size #14 ASTM after four cycles as a steel produced to fine grain practice, i.e., killed with silicon and alumi- 3U num.
TABLE III E new of mode of deoxidazion in response to short-cycle heatin g Austcnitc grain size Deoxidation practice Heating cycle Number of cycles Mean ASTM grain number do dian1.,
microns Coarse-grained 1,500 F. 8 sec. 2 3. 9 13.1 ASTM #2 to 4 1,500 F. 8 sec. 4 2. 8 14. 0 Fine-grained 1,500 F. 8 scc 2 3.3 13. 5 59 ASTM #5 to 8 1,500 1". 8 sec. 4 2.8 14. 0
1 McQuaid-Ehn Test.
Due to the ultrafine grain size, steels treated in accordance with this invention have better toughness, ductility and yield strength than conventionally heat treated steels.
This is shown by the following Table IV.
TABLE IV Mechanical properties [AISI 1045-0.28-Inch Thick Strip] Austcnitc Tensile Yield Elcng. Reduction Notch 1 Heat treatment grain size strength, strength, in 1", of area, toughness,
p.s.i. p.s.i. percent percent ft./lb.
at 25 F.
Conventional Normalize #8 ASTM. 101, 900 64, 100 28 57 11 (1,550 I air cool). Cyclical Rapid Hcatin #12 ASTM- 99, 200 73, 200 30. 5 61. 5 20 1 V-Notch Charpy Impact Test; Average of Three Half-Width Specimens.
bides, very little grain refinement can be obtained. However, a high degree of grain refinement can be obtained if the heating temperature is too low to dissolve all the carbides. Since for many uses solution of all carbides in high carbon steels is not required or desirable such steels While we have shown and described several specific embodiments of our invention, it will be understood that these embodiments are merely for the purpose of illustration and description and that various other forms .12.
be devised within the scope of our invention, as defined in the appended claims.
We claim:
1. A method of producing ultrafine grain size in steel which is predominately ferritic rather than austenitic at room temperature, becomes completely austenitic on heating to suitable elevated temperature and thereafter becomes ferritic on cooling to room temperature comprising cyclically treating such steel by heating it at least twice to above its A0 temperature but below the temperature at which austenite grains coarsen rapidly for just sufiicient time to transform it to an austenitic structure and then before any appreciable grain growth occurs quickly cooling it to transform the austenite in all but the last cycle to a microstructure of the class consisting of martensite, bainite or mixtures thereof and in the last cycle cooling at a rate which will produce the desired microstructure whereby an austenite grain size finer than ASTM is produced therein.
2. A method of producing ultrafine grain size in steel Which is predominately ferritic rather than austenitic at room temperature, becomes completely austenitic on heating to suitable elevated temperature and thereafter becomes ferritic on cooling to room temperature comprising cyclically treating such steel by heating it at least twice in less than seconds to above its Ac temperature but References Cited by the Examiner UNITED STATES PATENTS 1,919,983 7/33 Morrill 148-144 OTHER REFERENCES Principles of Heat Treatment by M. A. Grossmann, published by the A.S.M. (1935), page 203 relied upon.
DAV ID L. RECK, Primary Examiner.
UNITED STATES PATENT OFFICE CERTIFICATE 0F CORRECTION Patent No. 3, l78,3Z4 April 13, 1965 I Raymond A. 'Gra'nge et al. I It is hereby certified-that error appears in the above numbered pat ent requiring correction and that the said Letters Patent should read as corrected below.
Column 2, line 63, for "mulicycle" read multicycle line 49, for "on" read'" no Signed and sealed this 17th day of August 1965.
(SEAL) Altest:
ERNEST W. SWIDER EDWARD J. BRENNER Attesting Officer Commissioner of Patents

Claims (1)

1. A METHOD OF PRODUCING ULTRFINE GRAIN SIZE IN STEEL WHICH IS PREDOMINATELY FERRITIC RATHER THAN AUSTENITIC AT ROOM TEMPERATURE, BECOMES COMPLETELY AUSTENITIC ON HEATING TO SUITABLE ELEVATED TEMPERATURE AND THEREAFTER BECOMES FERRITIC ON COOLING TO ROOM TEMPERATURE COMPRISING CYCLICALLY TREATING SUCH STEEL BY HEATING IT AT LEAST TWICE TO ABOVE ITS AC1 TEMPERATURE BUT BELOW THE TEMPERATURE AT WHICH AUSTENITE GRAINS COARSEN RAPIDLY FOR JUST SUFFICIENT TIME TO TRANSFORM IT TO AN AUSTENITIC STRUCTURE AND THEN BEFORE ANY APPRECIABLE GRAIN GROWTH OCCURS QUICKLY COOLING IT TO TRANSFORM THE AUSTENITE IN ALL BUT THE LAST CYCLE TO A MICROSTRUCTURE OF THE CLASS CONSISTING OF MARTENSITE, BAINITE OR MIXTURES THEREOF AND IN THE LAST CYCLE COOLING AT A RATE WHICH WILL PRODUCE THE DESIRED MICROSTRUCTURE WHEREBY AN AUSTENITE GRAIN SIZE FINER THAN ASTM #10 IS PRODUCED THEREIN.
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Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3288657A (en) * 1962-08-08 1966-11-29 Yawata Iron & Steel Co Special heat treating method of steels
US3370994A (en) * 1965-11-29 1968-02-27 United States Steel Corp Method of softening steels
US3413166A (en) * 1965-10-15 1968-11-26 Atomic Energy Commission Usa Fine grained steel and process for preparation thereof
US3642595A (en) * 1969-09-23 1972-02-15 Us Air Force Thermal grain refinement of maraging steel
US3660176A (en) * 1970-02-10 1972-05-02 Armco Steel Corp Precipitation-hardenable stainless steel method and product
US3956989A (en) * 1966-12-08 1976-05-18 The United States Of America As Represented By The Secretary Of The Army Fragmentation device
US4032368A (en) * 1972-10-05 1977-06-28 United States Steel Corporation Intercritical-cycle annealing
US4040872A (en) * 1976-04-16 1977-08-09 Lasalle Steel Company Process for strengthening of carbon steels
US4109127A (en) * 1973-07-25 1978-08-22 Frank Frungel Apparatus and method for case hardening steel tools by application of heating pulses
DE2851142A1 (en) * 1978-11-25 1980-06-04 Neturen Co Ltd High tensile spring steel - is subjected to repeated surface induction heating to obtain extremely small grain size and increase fatigue strength
US4222799A (en) * 1978-11-14 1980-09-16 Neturen Company, Ltd. High-strength spring steel and its manufacturing process
US4362578A (en) * 1980-10-16 1982-12-07 Teledyne Industries, Inc. Method of hot working metal with induction reheating
US4486249A (en) * 1982-07-09 1984-12-04 Woodings Robert T Method of making class D sucker rods
WO1998048061A1 (en) * 1997-04-17 1998-10-29 Aspector Oy Heat treatment of steel
US6190472B1 (en) * 1993-03-16 2001-02-20 Ovako Steel Ab Method of soft annealing high carbon steel
CN1107728C (en) * 2000-04-25 2003-05-07 钢铁研究总院 Structural alloy steel crystallite superfining method
US6663730B2 (en) * 2000-11-17 2003-12-16 Imphy Ugine Precision Maraging steel and process for manufacturing a strip or a part cut out of a strip of cold-rolled maraging steel
US20040016530A1 (en) * 2002-05-08 2004-01-29 Schoen Jerry W. Method of continuous casting non-oriented electrical steel strip
US20070023103A1 (en) * 2003-05-14 2007-02-01 Schoen Jerry W Method for production of non-oriented electrical steel strip
CN101831530A (en) * 2010-04-29 2010-09-15 哈尔滨工程大学 Thermal treatment process for improving comprehensive mechanical property of low-alloy high-strength steel
CN104611533A (en) * 2015-02-06 2015-05-13 桂林理工大学 Heating method for refined No.35 steel austenite grains
CN104611531A (en) * 2015-02-06 2015-05-13 桂林理工大学 Heating method for refining austenite grains of 45 steel
CN104611527A (en) * 2015-02-06 2015-05-13 桂林理工大学 Heating method for refined 65# steel austenite grain
CN104611529A (en) * 2015-02-06 2015-05-13 桂林理工大学 Heating method for refined 75# steel austenite grain
US10408268B2 (en) * 2013-01-25 2019-09-10 Trane International Inc. Method of using pressure nitrided stainless steel hybrid bearing with a refrigerant lubricated compressor
US10577684B1 (en) 2017-11-13 2020-03-03 Mainstream Engineering Corporation Method for producing ultrafine-grained crystalline materials via electron beam processing
EP3617333A1 (en) 2018-08-27 2020-03-04 Roselli Oy Method for manufacturing a hypereutectoid steel product by thermomechanical processing

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US1919983A (en) * 1932-03-01 1933-07-25 Gen Electric Method for producing low loss nonaging silicon steel sheets

Patent Citations (1)

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Cited By (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3288657A (en) * 1962-08-08 1966-11-29 Yawata Iron & Steel Co Special heat treating method of steels
US3413166A (en) * 1965-10-15 1968-11-26 Atomic Energy Commission Usa Fine grained steel and process for preparation thereof
US3370994A (en) * 1965-11-29 1968-02-27 United States Steel Corp Method of softening steels
US3956989A (en) * 1966-12-08 1976-05-18 The United States Of America As Represented By The Secretary Of The Army Fragmentation device
US3642595A (en) * 1969-09-23 1972-02-15 Us Air Force Thermal grain refinement of maraging steel
US3660176A (en) * 1970-02-10 1972-05-02 Armco Steel Corp Precipitation-hardenable stainless steel method and product
US4032368A (en) * 1972-10-05 1977-06-28 United States Steel Corporation Intercritical-cycle annealing
US4109127A (en) * 1973-07-25 1978-08-22 Frank Frungel Apparatus and method for case hardening steel tools by application of heating pulses
FR2348274A1 (en) * 1976-04-16 1977-11-10 Lasalle Steel Co PROCESS FOR INCREASING THE RESISTANCE OF STEELS TO CARBON
US4040872A (en) * 1976-04-16 1977-08-09 Lasalle Steel Company Process for strengthening of carbon steels
US4222799A (en) * 1978-11-14 1980-09-16 Neturen Company, Ltd. High-strength spring steel and its manufacturing process
DE2851142A1 (en) * 1978-11-25 1980-06-04 Neturen Co Ltd High tensile spring steel - is subjected to repeated surface induction heating to obtain extremely small grain size and increase fatigue strength
US4362578A (en) * 1980-10-16 1982-12-07 Teledyne Industries, Inc. Method of hot working metal with induction reheating
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