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
  • C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
  • C21D9/36—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for balls; for rollers

Definitions

• the present invention relates to a heat-resisting steel, and more particularly to a heat-resisting steel with outstanding performance as a member for power plant, such as a high-temperature steam turbine rotor material and steam turbine, a heat treatment method for the heat-resisting steel and a high-temperature steam turbine rotor.
• a low alloy heat-resisting steel represented by 1Cr-1Mo-0.25V steel and a high Cr heat-resisting steel represented by 12Cr-1Mo—VNbN steel are used heavily.
• thermal power plants in these years are being made quickly to have a steam temperature raised higher, and the use of the high Cr heat-resisting steel having outstanding high-temperature properties is increasing.
• Parts configuring the center portion of the thermal power plant are formed of large-size materials, which are essentially required to be excellent in productivity and formability into desired shapes. And, they are required to have material properties which are not deteriorated but homogeneous even if formed into large parts.
• a conventional heat-resisting steel having chemical compositions disclosed in Japanese Patent No. 3,334,217 is poor in quenching property when used as large member and can hardly exert desired properties at the center portion of a steel ingot having a large drum diameter.
• the heat-resisting steel having the chemical compositions disclosed in Japanese Patent No. 3,439,197 has considerable segregation of components when a large steel ingot is cast and can hardly exert uniform material properties in the overall steel ingot.
• special dissolution is used to enhance the homogeneity of the steel ingot, the heat-resisting steel has drawbacks including advantages and disadvantages such as poor economical efficiency.
• the conventional heat-resisting steel contains a relatively large amount of ferrite former, such as Cr, Mo and W as reinforcing elements, so that the trend to generate a ferrite phase becomes high.
• ferrite former such as Cr, Mo and W
• the ferrite phase generated in a bainite phase is produced by chemical combination of the above-described ferrite former with Fe. Therefore, these elements which are added as the reinforcing elements are locally concentrated in the generated ferrite and have drawbacks that the contents of the elements in the bainitic structure decrease, and especially high-temperature strength is decreased.
• impact properties or toughness of the material may be degraded heavily.
• a heat-resisting steel having a bainite single phase structurer which can be used stably in a high temperature steam environment and has outstanding economical efficiency, a heat treatment method for the heat-resisting steel and a high-temperature steam turbine rotor.
• a heat-resisting steel of the present invention consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• a heat-resisting steel of the present invention consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• a heat-resisting steel of the present invention consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• the heat-resisting steels consisting of the bainite single phase structure can be formed by configuring in the ranges of the contents of the individual component elements.
• the heat-resisting steels excelling in high-temperature properties, toughness, embrittlement properties and the like and do not have a ferrite phase or the like which considerably decreases the material mechanical properties when the generated amount is increased can be provided.
• the above-described component elements Ti and/or N may be replaced by Fe and C.
• a heat treatment method for a heat-resisting steel of the present invention comprises heating to 980 to 1030° C. a steel ingot which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, cooling such that a cooling speed at the center portion of the steel ingot becomes at least 20° C./h or more, and conducting a tempering treatment.
• a heat treatment method for a heat-resisting steel of the present invention comprises heating to 980 to 1030° C. a steel ingot which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, cooling such that a cooling speed at the center portion of the steel ingot becomes at least 20° C./h or more, and conducting a tempering treatment.
• a heat treatment method for a heat-resisting steel of the present invention comprises heating to 980 to 1030° C. a steel ingot which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, cooling such that a cooling speed at the center portion of the steel ingot becomes at least 20° C./h or more, and conducting a tempering treatment.
• the heat-resisting steel comprising a bainite single phase structure that a ferrite phase is not formed, can be formed even if quenching is effected at a very slow cooling velocity of at least 20° C./h or more at the center portion of the steel ingot without forcedly cooling by, for example, a cooling medium such as water, oil or the like or an air blast.
• a high-temperature steam turbine rotor of the present invention comprises a heat-resisting steel which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• a high-temperature steam turbine rotor of the present invention comprises a heat-resisting steel which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, less than 0.01 of Ti, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• a high-temperature steam turbine rotor of the present invention comprises a heat-resisting steel which consists of, in percentage by weight, 0.25 to 0.35 of C, 0.15 or less of Si, 0.2 to 0.8 of Mn, 0.3 to 0.6 of Ni, 1.6 to 1.9 of Cr, 0.26 to 0.35 of V, 0.6 to 0.9 of Mo, 0.9 to 1.4 of W, 0.001 to 0.007 of N, 1.3 to 1.4 of a total of Mo and W/2 and the balance of Fe and inevitable impurities, wherein the heat-resisting steel consists of a bainite single phase structure securing 3.5 or more of a total amount of precipitates as 1.0 or more of Fe, 0.8 to 0.9 of Cr, 0.4 to 0.5 of Mo, 0.3 to 0.5 of W and 0.2 or more of V in percentage by weight are moved into the precipitates after a tempering heat treatment.
• a high-temperature steam turbine rotor comprising the bainite single phase structure can be formed by configuring in a range of the contents of the individual component elements described above.
• the high-temperature steam turbine rotor excelling in high-temperature properties, toughness, embrittlement properties and the like which does not have a ferrite phase or the like which considerably degrades the mechanical properties of the materials if the generated amount is increased.
• the above-described component element Ti and/or N may be replaced by Fe and C.
• the high-temperature steam turbine rotor is a high-pressure rotor, an intermediate pressure rotor or a high and intermediate pressure rotor. It is a rotor of a steam turbine which is operated with an exhaust temperature of 300° C. or more at the final stage outlet of the high-pressure portion of the high pressure rotor or the high and intermediate pressure rotor and an exhaust temperature of 200° C. or more at the final stage outlet of the intermediate pressure portion of the intermediate pressure rotor or the high and intermediate pressure rotor.
• the exhaust steam is introduced into a boiler or a low pressure turbine which is disposed separately.
• C is an element inevitable as a component element of a variety of carbides contributing to precipitation strengthening and secure quenching property. If its content is less than 0.25%, the above effects are small. If it exceeds 0.35 %, carbide coarsening is accelerated, and the trend of segregation is enhanced at the time of solidification of a steel ingot. Therefore, it is determined that the C content is in a range of 0.25 to 0.35%, and more desirably in a range of 0.27 to 0.33%.
• Si is useful as a deoxidizing element and improves the resistance to steam oxidation. But, if its content is high, the toughness is decreased and embrittlement is accelerated. Therefore, its content is desired to be as low as possible. If the Si content exceeds 0.15%, the above favorable properties are degraded considerably. Thus, the Si content is determined to be not more than 0.15% (excluding 0). And, the Si content is preferably not more than 0.1%.
• Mn is an element useful as a desulfurizing element but, if its content is less than 0.2%, its desulfurizing effect is not recognized, and if its added amount exceeds 0.8%, the creep strength is decreased. Therefore, the Mn content is determined to be in a range of 0.2 to 0.8%, and more preferably in a range of 0.4 to 0.8%.
• Cr is an element effective for oxidation resistance and corrosion resistance and also inevitable as a component element of carbonitride contributing to enhancement of precipitation.
• Cr is also useful as an element effective in improving the toughness. If the Cr content is less than 1.6%, the amount of Cr moved into carbonitride after the tempering heat treatment is little, and high-temperature stability of carbonitride cannot be secured. If the Cr content exceeds 1.9%, resistance to temper softening is decreased, desired normal-temperature strength cannot be secured, and the creep strength is decreased. Therefore, the Cr content is determined to be in a range of 1.6 to 1.9%.
• V contributes to the solid-solution strengthening and the formation of fine carbonitride. If the V content is 0.26% or more, fine precipitates are deposited sufficiently and to inhibit the recovering of the bainitic structure but, if its content exceeds 0.35%, the toughness is decreased, and coarsening of carbonitride is accelerated. Accordingly, the V content is determined to be in a range of 0.26 to 0.35%.
• W contributes to the solid-solution strengthening of the bainitic structure and the precipitation strengthening by becoming a component element of carbonitride. Especially, when W and Mo are added together, high-temperature stability of precipitates can be enhanced remarkably. W moves from the bainitic structure into precipitates with time while heating at a high temperature for a long period of time. Therefore, it is necessary to set the W content to 0.9% or more in order to keep the W content contributing to the solid-solution strengthening high for a long time of period. But, if the W content exceeds 1.4%, toughness is degraded, ferrite is prone to be generated, and the tendency of segregation of components of a large steel ingot is increased. Therefore, the W content is determined to be in a range of 0.9 to 1.4%, and more preferably in a range of 0.9 to 1.2%.
• Mo contributes to the solid-solution strengthening and the precipitation strengthening by becoming a component element of carbonitride. Especially, when Mo and W are added together, high-temperature stability of precipitates can be enhanced remarkably. Mo moves from the bainitic structure into precipitates with time while heating at a high temperature for a long period of time. Therefore, it is necessary to set the Mo content to 0.6% or more in order to keep the Mo content contributing to the solid-solution strengthening high for a long time of period. But, if the Mo content exceeds 0.9%, toughness is degraded, ferrite is prone to be generated, and the tendency of segregation of components of a large steel ingot is increased. Therefore, the Mo content is determined to be in a range of 0.6 to 0.9%, and more preferably in a range of 0.7 to 0.9%.
• N forms nitride or carbonitride and contributes to precipitation strengthening. Besides, N remaining in the bainitic structure also contributes to the solid-solution strengthening but, if the N content is less than 0.001%, the above effects are not recognized. Meanwhile, if the N content exceeds 0.007%, coarsening of nitride or carbonitride is accelerated, and the creep strength is decreased. Therefore, the N content is determined to be in a range of 0.001 to 0.007%.
• N can be substituted by increasing the C content within the range of the C content. Fe may be used instead of N.
• Ti is useful as adeoxidizing element. If the Ti content is less than 0.01%, it exerts a deoxidizing effect, and the remaining Ti is formed into solid solution. But, if the Ti content exceeds 0.01%, a generated amount of non-solid solution coarse Ti carbonitride increases, causing a decrease in toughness or weakening of the notch. Therefore, the Ti content is determined to be less than 0.01% (excluding 0). Inclusion of Ti in the above content allows decreasing the amount of O (oxygen) in the steel ingot by the deoxidizing effect, and oxide can also be prevented from being produced at the time of producing the steel ingot. Ti can be substituted by increasing the C content within the range of the C content. And, Fe may be used instead of Ti.
• Ni improves quenching property and toughness and has an effect to suppress ferrite from being generated. This effect is observed when the Ni content is 0.35 or more. But, if the Ni content exceeds 0.6%, the creep strength is decreased. Therefore, the Ni content is determined to be in a range of 0.3 to 0.6%.
• Inevitable impurities in the heat-resisting steel of the present invention include P (phosphorus), S (sulfur), Cu (copper), Al (aluminum), As (arsenic), Sn (tin), Sb (antimony) and O (oxygen). These impurities induce embrittlement when the heat-resisting steel is heated at a high temperature for a long time of period.
• W and Mo each have the effects as described in (6) and (7) above.
• the creep strength is improved better than when added separately, while the tendency of segregation of components of light elements increases considerably at the time of producing a large steel ingot.
• Mo equivalent an index called Mo equivalent (a total content of Mo and W/2 (% by weight)).
• the Mo equivalent a total content of Mo and W/2 (% by weight) is determined to be 1.3 to 1.4.
• the heat-resisting steel of the present invention is reinforced by the solid-solution strengthening of the bainitic structure and the precipitation of carbonitride.
• Carbonitride is precipitated intentionally by the tempering heat treatment, and the precipitates in the heat-resisting steel of the present invention are four kinds of M, VC, R type, M, RC type, M, QC type and MC type.
• M indicates a metal element.
• M in the M, VC, R type and M, RC type is mainly Fe and Cr, and Mo, W and the like might be contained additionally.
• M in the M, QC type is mainly Mo and W, and V might be contained additionally.
• M in the MC type is mainly V, and Mo and W might be contained additionally.
• the amount of precipitates was measured and identified as follows. A test sample was placed in a mixed liquid of methanol, acetylacetone and tetramethyl ammonium chloride and a bainitic structure was dissolved by electrolysis. After filtering, the resultant residue was washed and measured for its weight. And the value determined by dividing by the weights before and after the dissolving was used. Besides, the recovered residue was determined for the kinds of precipitates by X-ray analysis or the like.
• Fe in the precipitate is mainly a component element of M, VC, R type and M, RC type precipitates and contributes to precipitation strengthening. If the amount of Fe moved into the precipitate after the tempering heat treatment is less than 1.0%, the precipitated amount is small and the precipitation strengthening action does not work sufficiently. To exert the creep strength, it is effective to use the transformation with time after depositing as M,RC type precipitates after the tempering heat treatment but, if the moved amount of Fe is less than 1.0%, the precipitated amount of the M,RC type precipitate is small, so that the increase in creep strength cannot be expected by this method. Therefore, the Fe content in the precipitate after the tempering heat treatment was determined to be 1.0% or more.
• Cr in the precipitates is mainly a component element of M,VC,R type and M,RC type precipitates and contributes to precipitation strengthening. Cr substitutes for part of Fe in the precipitates, so that it also has an action to enhance the stability of the precipitates. If the amount of Cr moved into the precipitates after the tempering heat treatment is less than 0.8%, the precipitated amount is small, and the precipitation strengthening action does not work sufficiently. Meanwhile, if the amount of Cr moved into the precipitates after the tempering heat treatment exceeds 0.9%, disappearance of Fe,RC type precipitates is induced during the tempering heat treatment, and the time lapse effect described in (11) above cannot be exerted. Therefore, the Cr content in the precipitates after the tempering heat treatment was determined to be in a range of 0.8 to 0.9%.
• W in the precipitates is mainly a component element of the M, QC type precipitate and contributes to precipitation strengthening.
• W substitutes for part of the M, VC, R type, M, RC type and MC type precipitates, so that it enhances the high-temperature stability of the precipitates considerably. If the amount of W moved into the precipitates after the tempering heat treatment is less than 0.3%, the stability of the precipitates is low and a desired creep strength cannot be exerted. Meanwhile, if the amount of W moved into the precipitates after the tempering heat treatment exceeds 0.5%, the solid solution amount of W in the bainitic structure decreases, and the solid-solution strengthening amount at a high temperature decreases. Therefore, the W content in the precipitates after the tempering heat treatment was determined to be in a range of 0.3 to 0.5%.
• Mo in the precipitates is mainly a component element of M, QC type precipitate and contributes to precipitation strengthening. Mo substitutes for part of the M, VC, R type, M, RC type and MC type precipitates and enhances the high-temperature stability of the precipitates considerably. If the amount of Mo moved into the precipitates after the tempering heat treatment is less than 0.4%, the stability of the precipitates is low, and a desired creep strength cannot be exerted. Meanwhile, if the amount of Mo moved into the precipitates after the tempering heat treatment exceeds 0.5%, the solid solution amount of Mo in the bainitic structure decreases, and the solid-solution strengthening amount at a high temperature decreases. Therefore, the Mo content in the precipitates after the tempering heat treatment was determined to be in a range of 0.4 to 0.5%.
• V in the precipitates is mainly a component element of fine MC type precipitate and contributes to precipitation strengthening.
• V substitutes for part of the M, VC,R type, M, RC type and M, QC type precipitates and enhances the high-temperature stability of the precipitates considerably. If the amount of V moved into the precipitates after the tempering heat treatment is less than 0.2%, the precipitated amount of the MC type precipitate decreases, and the stability of the other precipitates becomes low. Therefore, the V content in the precipitates after the tempering heat treatment was determined to be 0.2% or more.
• the total amount of the precipitates is required to be 3.5% or more. If the total amount is less than 3.5%, strength characteristics and high-temperature stability of the precipitates are decreased as described in the above (11) through (15). Therefore, the total content of the precipitates after the tempering heat treatment was determined to be 3.5% or more.
• the heat-resisting steel configuring the high-temperature steam turbine rotor of the present invention is different from the ordinary heat-resisting steel, and the solid solution amount and the precipitated amount of the carbonitride change with time during the operation, causing exertion of outstanding high-temperature properties.
• Mo and W which are in the supersaturated solid solution state in the heat-resisting steel mainly move into the M, QC type precipitate and the MC type precipitate with time, to enhance the their high-temperature stability, the M, RC type precipitate having Fe as a main component element transforms into M, VC, R type precipitate which is more stable than when having Cr as the main component element with time to keep the creep strength.
• the latter involves dissolution of Fe in the M, RC type precipitate deposited in a large amount by the tempering heat treatment, so that the total amount of precipitates decreases in comparison with that after the tempering heat treatment.
• the remaining M, RC type precipitate has an effect of keeping the creep strength but, if the total amount of precipitates is less than 2.8%, the M, RC type precipitate is eliminated completely, and the precipitation strengthening action is decreased rapidly. Therefore, the total amount of precipitates after the operation for 100,000 hour equivalent was determined to be 2.8% or more.
• Precipitates deposited in the heat-resisting steel configuring the high-temperature steam turbine rotor are different in precipitated amount depending on their types, and their precipitated amount are variable with time depending on the operation of the high-temperature steam turbine rotor, but no new type of precipitate is deposited when operating. And the maximum temperature of steam during a steady operation is in a range of approximately 540 to 580° C.
• the grain diameter of prior austenite is preferably 100 ⁇ m or less in average.
• the prior austenite grain diameter has no small effect on the individual mechanical properties. If it exceeds 100 ⁇ m, ductility is lowered, crack at grain boundary is caused easily, notch creep strength and toughness are decreased. Therefore, the prior austenite grain diameter was determined to be 100 ⁇ m or less in average.
• the grain diameter is finally determined depending on the heating temperature at the time of quenching.
• a heating temperature 980 to 1030° C. is desirable. If the heating temperature is less than 980° C., a sufficient quenching effect cannot be obtained, and desired mechanical properties cannot be exerted. Meanwhile, if the heating temperature exceeds 1030° C., the grains become coarse considerably. The property is decreased considerably with the above-described coarsening of the grains.
• the heat-resisting steel and high-temperature steam turbine rotor of the present invention contain the elements of the above-described (1) through (10) in a prescribed range, the Mo equivalent is in a prescribed range, and the prior austenite grain diameter is 100 ⁇ m or less in average. And, the elements described in the above (11) and (12) are contained in a prescribed range within the precipitates. After the operation for 100,000 hour equivalent in the vicinity of the portion of the high-temperature steam turbine rotor exposed to steam at the maximum temperature at the time of a steady operation, the total amount of precipitates can be secured at a prescribed value or more, and desired mechanical properties can be exerted accordingly.
• the heat-resisting steel of the present invention is determined to have the added range of the individual added elements ((1) through (10)) so as to have a bainite single phase structure.
• the ferrite phase may be generated depending on the heating temperature at the time of production or the cooling conditions after the heating. Especially, where heating and cooling are repeated in the production process and the steam turbine rotor material has a large material size, a ferrite phase is generated depending on, for example, a cooling speed at the time of quenching.
• the ferrite phase has a feature that it is generated when exposed to a prescribed temperature range for a prescribed time of period. For example, if the cooling speed at the time of quenching is low, it passes through the generation region in the cooling step. As a result, the structure with the ferrite phase generated in the bainite structure is obtained, and the properties are degraded.
• the heat-resisting steel and high-temperature steam turbine rotor having the component range according to the present invention can be provided with a bainite single phase structure having good mechanical properties at a high temperature without limiting the cooling speed.
• a stable operation can be conducted in a high-temperature steam environment, and it is good in economical efficiency.
• the sample steels in the first embodiment were produced by dissolving about 30 kg of material having the chemical composition range of the present invention, casting it, hot forging the cast ingot, performing annealing, normalizing and quenching, and tempering.
• the quenching was performed at 980 to 1030° C. on the cast ingot after the normalizing such that the cooling speed approximately in the center of the cast ingot became 20 to 80° C./h.
• Table 1 shows chemical compositions of the produced sample steels.
• steel type P1 through steel type P 14 are heat-resisting steels having compositions in the range according to the present invention.
• steel type C1 through steel type C6 are heat-resisting steels having compositions which are not in the chemical compositions in the range according to the present invention and are comparative examples.
• Table 1 also shows the remaining amounts of oxygen of the individual steel types.
• the numeric values in Table 1 are in % by weight.
• the remaining amount of oxygen in the sample steels containing Ti is at most 10 ppm. This value is lower than the remaining amount of oxygen in the sample steels not containing Ti, indicating that the deoxidization by addition of Ti is effectively working.
• the steel type C2 has a deoxidizing effect but generates Ti carbonitride in a state of non-solid solution.
• the steel types shown in Table 1 are adjusted to have the 0.02% proof stress of approximately 660 to 690 MPa at normal temperature suitable for the turbine rotor as shown in Table 2.
• notched test pieces for Charpy impact test according to JIS Z 2202 having a thickness of 2 mm and V notch were prepared, and a Charpy impact test with these test pieces was conducted.
• the test results are shown in Table 2.
• Table 2 also shows the measured results of rupture time of a creep rupture test under conditions of 600° C. and 196 MPa.
• the steel types P1 through P14 of the embodiment in the chemical composition range of the present invention had 50 to 55J impact absorption energy at 20° C. Meanwhile, the steel types C1 to C6 of the comparative example had impact absorption energy of at most 40J at 20° C., and the impact absorption energy was generally lower than in the embodiment.
• Rupture time in the creep rupture test conducted on the individual steels under conditions of 600° C. and 196 MPa was about 1850 hours at shortest for the steel types P1 through P14 of the embodiment.
• creep rupture time of the steel types C1 through C6 of the comparative example was 800 to 1530 hours.
• the steel type C1, steel type C3 and steel type C5 which had a relatively long rupture time had impact absorption energy at 20° C. considerably lower than those of the individual steel types of the embodiment.
• Mo equivalent the total content of Mo and W/2 (% by weight)
• Mo equivalent exceeds 1.4 as the steel type C5 has
• the creep rupture time is short clearly.
• the Mo equivalent is in a range of 1.3 to 1.4, the creep rupture time was short and the impact absorption energy was low if the added amounts of the other elements are not within the chemical composition range of the present invention.
• the heat-resisting steels having the chemical composition range of the present invention are desirably adjusted to a state of securing a prescribed precipitated amount when they are subjected to the tempering heat treatment.
• the steel type P1, the steel type P6, the steel type P11 and the steel type P14 shown in Table 1 were quenched from 990° C., such that the cooling speed approximately at the center of the sample steels becomes 20 to 80° C./h, and subjected to the tempering heat treatment at 630 to 730° C.
• Table 3 shows the contents (% by weight) of Fe, Cr, Mo, W and V among the elements contained in the precipitates after the tempering heat treatment of the sample steels and the total amount (% by weight) of the precipitates. Table 3 also shows the measures results of rupture time of the creep rupture test conducted on the sample steels under conditions of 600° C. and 196 MPa.
• the heat-resisting steels which satisfy the contents of the elements contained in the precipitates of the present invention and have the total amount not smaller than the total amount (3.5% by weight or more) of the precipitates of the present invention exert excellent creep rupture property.
• the heat-resisting steels shown in the embodiment can secure not only the creep rupture property but also sufficient impact absorption energy as it is presumable from the results of the steel type P1, the steel type P6, the steel type P11 and the steel type P14 in Table 2.
• the heat-resisting steels in the chemical composition range of the present invention are subjected to the tempering heat treatment, they are adjusted to a state securing a prescribed precipitated amount, and the total amount of the precipitates is desirably secured at 2.8% by weight or more in the vicinity of the portion exposed to a high-temperature steam at a prescribed temperature for 100,000 hour equivalent.
• heat-resisting steels of the steel type P2, steel type P7, steel type P10 and steel type P13 shown in Table 1 that the total amount of the precipitates after the tempering heat treatment satisfies the content range of the elements contained in the precipitates of the present invention, and the total amount of the precipitates is not less than the total amount (3.5% by weight or more) or more of the precipitates of the present invention were determined as sample steels. And, the sample steels were heated at a temperature in a range of 550 to 600° C. for 100,000 hour equivalent.
• Table 4 shows the measured results of the total amount of the precipitates after the tempering heat treatment, the total amount of the precipitates after heating for 100,000 hour equivalent and the measured results of the rupture time by the creep rupture test under conditions of 600° C. and 196 MPa.
• the heat-resisting steel in the chemical composition range of the present invention is suitable for the production of a steel ingot which has small segregation of component concentration and is homogeneous.
• the cast ingot produced by using a mold having a value about 1.5 obtained by dividing the height of the mold at the time of casting by the diameter of the mold was analyzed for component concentration in a height direction at the center portion of the cast ingot after solidification.
• Table 5 shows the analyzed results of the component concentration of C which is the lightest element and W which is the heaviest element among those configuring the above-described steel type.
• the values in Table 5 are values obtained by dividing the component concentration of the individual portions of the steel ingot by the component concentration of a molten metal. And, the distance 100% from the bottom of the steel ingot indicates the top end of the steel ingot.
• the steel type P3, the steel type P7, the steel type P12 and the steel type P13 shown in Table 1 were used as sample steels.
• the grain diameters of the sample steels were adjusted by hot working, then they were adjusted to the 0.02% proof stress of about 660 to 690 MPa at normal temperature suitable for the turbine rotor.
• sample steels were measured for the grain diameter by the test method described in JIS G 0551. And, reduction of area at 300° C. was measured according to the method of tensile test described in JIS Z 2241. In addition, it was measured whether the notch creep rupture strength by the creep rupture test at 300° C. was enhanced or reduced in comparison with a lubricating material.
• Table 6 shows the results of the above-described measurements.

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