This invention relates to the casting of steel strip. It has particular application for continuous casting of thin steel strip less than 5 mm in thickness in a roll caster.
In a roll caster, molten metal is cooled on casting surfaces of at least one casting roll and formed into thin cast strip. In roll casting with a twin roll caster, molten metal is introduced between a pair of counter rotated casting rolls that are cooled. Solidified metal shells are formed on the moving casting surfaces and are brought together at a nip between the casting rolls to produce thin cast strip delivered downwardly from the nip. The term “nip” is used herein to refer to the general region in which the casting rolls are closest together. In any case, the molten metal is usually poured from a ladle into a smaller vessel, and from there, flows through a metal delivery system to distributive nozzles located generally above the nip between the casting rolls. During casting, the molten metal is delivered between the casting rolls to form a casting pool of molten metal supported on the casting surfaces of the rolls adjacent the nip and along the length of the casting rolls. Such casting pool is usually confined between side plates or dams, which are held in sliding engagement adjacent the ends of the casting rolls, so as to confine the two ends of the casting pool.
When casting thin steel strip with a twin roll caster, the molten metal in the casting pool will generally be at a temperature of the order of 1500° C. and above. It is therefore necessary to achieve very high cooling rates over the casting surfaces of the casting rolls. A high heat flux and extensive nucleation on initial solidification of the metal shells on the casting surfaces is needed to form the steel strip. U.S. Pat. No. 5,760,336, incorporated herein by reference, describes how the heat flux on initial solidification can be increased by adjusting the steel melt chemistry such that a substantial portion of the metal oxides formed are liquid at the initial solidification temperature, and in turn, a substantially liquid layer is formed at the interface between the molten metal and casting surfaces. As disclosed in U.S. Pat. Nos. 5,934,359 and 6,059,014 and International Application AU 99/00641, the disclosures of which are incorporated herein by reference, nucleation of the steel on initial solidification can be influenced by the texture of the casting surface. In particular, International Application AU 99/00641 discloses that a random texture of discrete protrusions formed in the casting surfaces can enhance initial solidification by providing substantial nucleation sites distributed over the casting surfaces.
Attention has been given in the past to the steel chemistry of the melt, particularly in the ladle metallurgy furnace before thin strip casting. We have given attention in the past to the oxide inclusions and the oxygen levels in the steel metal, and their impact on the quality of the steel strip produced. We have also found that the quality of the steel strip and the production of the thin steel strip is also enhanced by control of the hydrogen levels and nitrogen levels in the molten steel. Controlling hydrogen and nitrogen levels has in the past been the subject of investigation in slab casting, but to our knowledge has not been a focus of attention in thin strip casting until our work. For example, see Control of Heat Removal in the Continuous Casting Mould, by P. Zasowski and D. Sosinsky, 1990 Steelmaking Conference Proceedings, 253-259; and Determination and Prediction of Water Vapor Solubilities in CaO—MgO—SiO2 Slags, by D. Sosinsky, M. Maeda and A. Mclean, Metallurgical Transactions, vol. 16b, 61-66 (March 1985).
We have also described in parent U.S. patent application Ser. No. 10/961,300, filed Oct. 8, 2004, and U.S. provisional patent application 60/510,479, filed Oct. 10, 2003, that controlling the hydrogen level to below about 6.9 ppm and the nitrogen level to below about 120 ppm, while maintaining the sum of the partial pressures of hydrogen and nitrogen to not more than 1.15 atmospheres is a substantial advance in thin strip casting. We described that by controlling the hydrogen and nitrogen levels in plain carbon steel strip unique composition and production qualities can be produced by roll casting.
Now, we have found that the amount of heat flux from the metal shells is sensitive to the nitrogen levels in the molten steel in the casting pool, and therefore, by controlling the nitrogen levels in the casting pool the heat flux between the molten metal and the casting rolls can be controlled. Disclosed is a method of casting steel strip comprising the steps of:
determining a desired heat flux set point in casting thin cast strip from molten metal from a casting pool between casting rolls in a twin roll caster;
calculating the heat flux during casting of thin steel strip from molten metal in the casting pool in the twin roll caster; and
changing the nitrogen concentration in the casting pool to adjust the heat flux to the desired heat flux set point.
The nitrogen concentration in the casting pool may be controlled during the casting campaign to adjust for changes roughness of the casting rolls and other operating conditions to maintain the calculated heat flux to the desired heat flux set point or some adjustment therefrom as desired. The controlling step may be done manually by an operator or done automatically by a proportional controller.
Also disclosed is a method of casting thin steel strip comprising the steps of:
introducing molten plain carbon steel on casting surfaces of at least one casting roll with the molten steel having a nitrogen content below about 120 ppm and a hydrogen content below about 6.9 ppm and such that the sum of partial pressure of nitrogen and partial pressure of hydrogen is no more than 1.15 atmospheres;
forming a casting pool of molten metal on the casting surfaces of the casting roll;
causing the nitrogen level in the molten metal in the casting pool to vary depending on casting speed and strip thickness to control heat flux between the casting pool and the surfaces of the casting roll to a desired value; and
solidifying the molten steel to form metal shells on the casting rolls having nitrogen and hydrogen levels reflected by the content thereof in the molten steel to form thin steel strip.
The method of casting steel strip nay be carried out by the steps comprising the following:
assembling a pair of cooled casting rolls having a nip between them and confining end closures adjacent to ends of the casting rolls;
introducing molten plain carbon steel between the pair of casting rolls to form a casting pool on the casting rolls with the end closures confining the pool, with the molten steel having a nitrogen content below about 120 ppm and a hydrogen content below about 6.9 ppm and such that the sum of partial pressure of nitrogen and partial pressure of hydrogen is no more than 1.15 atmospheres;
causing the nitrogen level in the molten metal in the casting pool to be varied depending on casting speed and strip thickness to control heat flux between the casting pool and the surfaces of the casting roll to a desired value;
counter-rotating the casting rolls and solidifying the molten steel to form metal shells on casting surfaces of the casting rolls having nitrogen and hydrogen levels reflected by the content of the molten steel to provide for the formation of thin steel strip; and
forming solidified thin steel strip through the nip between the casting rolls to produce a solidified steel strip delivered downwardly from the nip.
In any of these methods, nitrogen level in the molten melt in the casting pool may be controlled by introducing the nitrogen in the metal delivery system, e.g. in the tundish, above the casting pool. In any of these methods, the nitrogen levels in the casting pool may be maintained below 100 ppm or 85 ppm. In any of these methods, the hydrogen content may be between 1.0 and 6.5 ppm.
In any of these methods, the heat flux can be indirectly correlated with the sum of the calculated partial pressures of nitrogen and hydrogen in the casting pool. The sum of the partial pressures of nitrogen and hydrogen calculated from the concentrations of nitrogen and hydrogen in the molten metal of the casting pool may be no more than 1.15 atmospheres, or may be between 0.1 and 0.8 atmospheres. Note that the partial pressures of nitrogen and of hydrogen are calculated from the levels, or concentrations, of nitrogen and hydrogen in the casting pool. See Richard J. Fruehan, ed., The Making, Shaping and Treating of Steel § 2.4.2.1 Table 2.9 (11th ed. 1998). As a practical matter, the nitrogen and hydrogen concentrations are typically measured in the tundish adjacent the casting pool, and it is the measured levels of nitrogen and hydrogen in the tundish that are reported herein. There is typically a slight nitrogen pick up of the molten metal between the tundish and the casting pool; however, the concentrations of the nitrogen and hydrogen in the casting pool are believed to be the concentrations related to control of the heat flux.
The method of casting steel strip may include the steps of correlating the heat flux with the sum of the calculated partial pressures of hydrogen and nitrogen associated the nitrogen and hydrogen concentrations in the casting pool, measuring the hydrogen and nitrogen concentrations in the molten metal going into the casting pool during casting, calculating the sum of the partial pressures associated with the measured hydrogen and nitrogen concentrations, and changing the concentration of nitrogen in the casting pool to provide the sum of the calculated partial pressures associated with the hydrogen and nitrogen concentrations correlated with the desired heat flux.
Plain carbon steel for purpose of the present invention is defined as less than 0.65% carbon, less than 2.5% silicon, less than 0.5% chromium, less than 2.0% manganese, less than 0.5% nickel, less than 0.25% molybdenum and less than 0.05% aluminum, together with of other elements such as sulfur, oxygen and phosphorus which normally occur in making carbon steel by electric arc furnace. Low carbon steel may be used in these methods having a carbon content in the range 0.001% to 0.1% by weight, a manganese content in the range 0.01% to 2.0% by weight, and a silicon content in the range 0.01% to 2.5% by weight. The steel may have an aluminum content of the order of 0.05% or less by weight. The aluminum may, for example, be as little as 0.008% or less by weight. The molten steel may be a silicon/manganese killed steel.
In these methods, the sulfur content of the steel maybe 0.01% or less. For example, the sulfur content of the steel may be 0.007% by weight.
The nitrogen and hydrogen levels are the dissolved nitrogen and hydrogen in the molten metal, and not nitrogen and hydrogen combined with other elements in compounds in the molten metal. In these methods, the nitrogen may be measured by optical emission spectrometry, calibrated against the thermal conductivity method as described below. The hydrogen levels may be determined by a Hydrogen Direct Reading Immersed System (“Hydris”) unit, made by Hereaus Electronite.
The maximum allowable nitrogen and hydrogen levels in the casting pool may be associated with the sum of the calculated partial pressures of hydrogen and nitrogen and may be such as to not exceed 1.15 or 1.0 atmospheres. Higher pressures may be utilized in certain conditions, and the associated levels of nitrogen and hydrogen can be corresponding higher. For example, as explained below, a ferrostatic head may be 1.15, causing the nitrogen levels and hydrogen levels to be higher in the casting pool. But for purposes of the parameters of the present methods, the partial pressures of nitrogen and hydrogen are calculated from the measured levels of nitrogen and hydrogen in the molten metal using the equation described below. The calculated partial pressure would be the gas pressure that the nitrogen or hydrogen exerts in equilibrium with the liquid steel; the partial pressures of nitrogen and hydrogen in the casting pool are during a casting campaign usually determined by the gases injected into the chamber in which the casting pool is formed.
The present invention provides cast steel strip with unique properties that are described by the methods by which it is made. This steel strip may be described as plain carbon steel.
In order that the invention may be more fully explained, illustrative results of experimental work carried out to date will be described with reference to the accompanying drawings in which:
As shown in
Casting pool 31 is confined at the ends of the casting rolls 22 by a pair of side closure plates (not shown), which are adjacent to and held against stepped ends of the casting rolls when the roll carriage is at the casting station. Side closure plates are illustratively made of a strong refractory material, for example boron nitride composite, and have scalloped side edges to match the curvature of the stepped ends of the rolls. The side plates can be mounted in plate holders which are movable at the casting station by actuation of a pair of hydraulic cylinder units (or other suitable means) to bring the side plates into engagement with the stepped ends of the casting rolls to form end closures for the molten pool of metal formed on the casting rolls during a casting operation.
Frame 21 supports a casting roll carriage (not shown) which is horizontally movable between a mounting station and a casting station. The casting roll carriage supports the casting rolls 22, and is able to move the casting rolls 22 as an assembly from a mounting station to the casting station in the caster.
Casting rolls 22 are internally water cooled so that metal shells solidify on the moving casting surfaces 22A and 22B of the casting rolls 22 in the casting pool 31. The shells are then brought together at the nip 29 between the casting rolls to produce the solidified strip 12, which is delivered downwardly from the nip.
Casting rolls 22 are counter-rotated through drive shafts (not shown) driven by an electric, hydraulic or pneumatic motor and transmission. Each casting roll 22 may have copper peripheral walls adjacent the casting surfaces 22A and 22B. coated with chromium, or nickel or some other suitable hard coating. Formed in each casting roll 22 is a series of longitudinally extending and circumferentially spaced water cooling passages to supply cooling water. The casting rolls 22 may typically be about 500 mm in diameter, and may be up to 1200 mm or more in diameter. The casting rolls 22 may be up to about 2000 mm, or longer, in order to produce strip product of about 2000 mm wide, or wider.
Tundish 23 is of conventional construction. It is formed as a wide dish made of a refractory material such as for example magnesium oxide (MgO). One side of the tundish receives molten metal from the ladle, and an overflow spout and an emergency plug (not shown) may be provided at the other side if desired.
Delivery nozzle 30 is formed as an elongated body made of a refractory material such as for example alumina graphite or zirconia graphite. Its lower part is tapered so as to converge inwardly and downwardly above the nip between casting rolls 22, and to be submerged in the casting pool 31. Delivery nozzle 30 may have a series of horizontally spaced, generally vertically extending flow passages to produce a suitably low horizontal discharge of molten metal along the width of the casting rolls and to deliver the molten metal in the casting pool 31 onto the roll surfaces 22A and 22B where solidification occurs. The delivery nozzle may be a described in more detail in U.S. Pat. No. 6,012,508, which is incorporated here in by reference.
The twin roll caster may be of the kind illustrated and described in some detail in, for example, U.S. Pat. Nos. 5,184,668; 5,277,243; 5,488,988; and/or 5,934,359; U.S. patent application Ser. No. 10/436,336; and International Patent Application PCT/AU93/00593, the disclosures of which are incorporated herein by reference. Reference may be made to those patents for appropriate construction details but forms no part of the present invention.
Results of the control of the nitrogen and hydrogen levels, or concentrations, in the casting pool 31 in making thin cast sheets of plain carbon steel are set forth in
Specifically, referring to
The heat flux data reported in
Moreover, we have found as disclosed herein that there is a correlation between the concentration of nitrogen in the steel melt and the amount of heat flux from the molten metal in the casting pool to the casting rolls. As illustrated in
As demonstrated in
Specifically, in the casting process measured in
Cast steel strip is produced using the casting method by introducing molten plain carbon steel on casting surfaces 22A and 22B of casting rolls 22, with the molten steel having a nitrogen concentration below about 120 ppm and a hydrogen concentration below about 6.9 ppm, and such that the sum of partial pressure of nitrogen and partial pressure of hydrogen is no more than 1.15 atmospheres, forming a casting pool of molten metal on the casting surfaces of the casting rolls, causing the nitrogen concentration in the molten metal in the casting pool to be varied depending on casting speed and strip thickness to control heat flux between the casting pool and the casting roll to a desired value, and solidifying the molten steel to form metal shells on the casting rolls having nitrogen and hydrogen concentrations reflected by the content thereof in the molten steel to form thin steel strip.
It is contemplated that a desired heat flux and nitrogen concentration in the casting pool can be maintained and controlled by monitoring and controlling the concentration of nitrogen entering the casting pool, e.g., in tundish 23. Prior to casting, the molten steel may be treated by a vacuum degassing that reduces the amounts of nitrogen and hydrogen in the steel melt. However, thereafter, a desired nitrogen concentration in the molten metal in the casting pool may be maintained by monitoring and changing a controlled amount of nitrogen. One method of changing nitrogen concentration in the molten metal of the casting pool is by introducing nitrogen gas into the tundish 23 through a lance 39, as shown on
The graph of
Where H and N are hydrogen and nitrogen concentrations in ppm, pH and pN are partial pressures of hydrogen and nitrogen in atmospheres, and T is temperature in ° K. See, Richard J. Fruehan, ed., The Making, Shaping and Treating of Steel § 2.4.2.1 Table 2.9 (11th ed. 1998). Also shown in
This
This
Accordingly, one method for controlling the concentration of nitrogen in the molten steel includes the steps of measuring the concentrations of nitrogen and hydrogen in the molten steel, calculating the sum of the partial pressure of nitrogen and the partial pressure of hydrogen from the measured concentrations of nitrogen and hydrogen in the molten steel, calculating the amount of nitrogen that needs to be changed to make the sum of nitrogen and hydrogen partial pressures equal a predetermined value for achieving a desired heat flux, and changing the concentration of nitrogen in the casting pool to achieve the nitrogen concentration related to a targeted sum of the calculated partial pressure of nitrogen and hydrogen. The sums of the calculated pressures of nitrogen and hydrogen is no more than 1.15 atmospheres, and if desired to reach a correlated set point heat flux, between 0.1 and 0.8 atmospheres as shown in
Cast steel strip is produced in one casting method by introducing molten plain carbon steel on casting surfaces of at least one casting roll, with the molten steel having a nitrogen concentration below about 120 ppm and a hydrogen concentration below about 6.9 ppm, and such that the sum of partial pressure of nitrogen and partial pressure of hydrogen is no more than 1.15 atmospheres, forming a casting pool of molten metal on the casting surfaces of the casting roll, varying the nitrogen concentration in the molten metal in the casting pool depending on casting speed and strip thickness to control heat flux between the casting pool and the surfaces of the casting roll to a desired value, and solidifying the molten steel to form metal shells on the casting rolls having nitrogen and hydrogen concentrations reflected by the content thereof in the molten steel to form this steel strip.
A desired heat flux may be maintained when the sum of the partial pressure of nitrogen and the partial pressure of hydrogen in the melt is no more than 1.15 atmosphere, indicated by the graph line 41 in
In casting method, the concentration of hydrogen in the steel melt is less than about 6.9 ppm. The concentration of hydrogen may be between 1.0 and 6.5 ppm. It is contemplated that the concentration of nitrogen will be below about 120 ppm. The concentration of nitrogen may be below about 100 ppm or below about 85 ppm.
The nitrogen was determined by analysis with optical emission spectrometry (“OES”) calibrated against the thermal conductivity (“TC”) method on a scheduled basis. Optical emission spectrometry (OES) using arc and spark excitation is the preferred method to determine the chemical composition of metallic samples. This process is widely used in the metal making industries, including primary producers, foundries, die casters and manufacturing. Due to its rapid analysis time and inherent accuracy, Arc/Spark OES systems are most effective in controlling the processing of alloys. These spectrometers may be used for many aspects of the production cycle including in-coming inspection of materials, metal processing, quality control of semi-finished and finished goods, and many other applications where a chemical composition of the metallic material is required.
The Thermal Conductivity (TC) method, used to calibrate the OES, typically employs a microprocessor-based, software controlled instrument that can measure nitrogen, as well as oxygen, in a wide variety of metals, refractories and other inorganic materials. The TC method employs the inert gas fusion principle. A weighed sample, placed in a high purity graphite crucible, is fused under a flowing helium gas stream at temperatures sufficient to release oxygen, nitrogen and hydrogen. The oxygen in the sample, in all forms present, combines with the carbon from the crucible to form carbon monoxide. The nitrogen present in the sample releases as molecular nitrogen and any hydrogen is released as hydrogen gas.
In the TC method, oxygen is measured by infrared absorption (IR). Sample gases first enter the IR module and pass through CO and CO2 detectors. Oxygen present as either CO or CO2 is detected. Following this, sample gas is passed through heated rare-earth copper oxide to convert CO to CO2 and any hydrogen to water. Gases then re-enter the IR module and pass through a separate CO2 detector for total oxygen measurement. This configuration maximizes performance and accuracy for both low and high range.
In the TC method, nitrogen is measured by passing sample gases to be measured through heated rare-earth copper oxide which converts CO to CO2 and hydrogen to water. CO2 and water are then removed to prevent detection by the TC cell. Gas flow then passes through the TC cell for nitrogen detection.
As stated above, the hydrogen is measured by a Hydrogen Direct Reading Immersed System (“Hydris”) unit, made by Hereaus Electronite. This unit is believed to be described in the following referenced US patents: U.S. Pat. Nos. 4,998,432; 5,518,931 and 5,820,745.
While the invention has been illustrated and described in detail in the foregoing drawings and description, the same is to be considered as illustrative and not restrictive in character, it being understood that only illustrative embodiments thereof have been shown and described and that all changes and modifications that come within the spirit of the invention are desired to be protected. Additional features of the invention will become apparent to those skilled in the art upon consideration of the description. Modifications may be made without departing from the spirit and scope of the invention.
This application is a continuation in part that claims priority to and the benefit of U.S. patent application Ser. No. 10/961,300 filed Oct. 8, 2004, and U.S. provisional patent application 60/510,479 filed Oct. 10, 2003, both of which are incorporated herein by reference.
Number | Date | Country | |
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60510479 | Oct 2003 | US |
Number | Date | Country | |
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Parent | 10961300 | Oct 2004 | US |
Child | 11548493 | Oct 2006 | US |