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AU598398B2 - Mold additive for continuous casting of steel - Google Patents
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AU598398B2 - Mold additive for continuous casting of steel - Google Patents

Mold additive for continuous casting of steel Download PDF

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Publication number
AU598398B2
AU598398B2 AU23687/88A AU2368788A AU598398B2 AU 598398 B2 AU598398 B2 AU 598398B2 AU 23687/88 A AU23687/88 A AU 23687/88A AU 2368788 A AU2368788 A AU 2368788A AU 598398 B2 AU598398 B2 AU 598398B2
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AU
Australia
Prior art keywords
weight
sio
mold
cao
amount
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Ceased
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AU23687/88A
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AU2368788A (en
Inventor
Hideaki Fujiwara
Kenji Ichikawa
Yoichiro Kawabe
Akihiro Morita
Osamu Nomura
Koyo Yanagawa
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Shinagawa Refractories Co Ltd
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Shinagawa Refractories Co Ltd
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Publication of AU2368788A publication Critical patent/AU2368788A/en
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/10Supplying or treating molten metal
    • B22D11/11Treating the molten metal
    • B22D11/111Treating the molten metal by using protecting powders

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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Continuous Casting (AREA)
  • Treatment Of Steel In Its Molten State (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Description

COMMONWEALTH OF AUSTRALIA 1102A:rk th-f00) 2 9 121/ 1 E3
I
598398 tALIA Form COMMONWEALTH OF AUSTI PATENTS ACT 1952 COMPLETE SPECIFICATION FOR OFFICE USE Short Title: Int. Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: Priority: amendments made under Section 49 anld is correct for printing.
Related Art: I'I- TO BE COMPLETED BY APPLICANT Name of Applicant: Address of Applicant: Actual Inventor: Address for Service: SHINAGAWA REFRACTORIES CO., LTD.
2-1, Ohtemachi 2-chome, Chiyoda-ku, TOKYO, JAPAN Kenji Ichikawa; Osamu Nomura; Akihiro Morita; Yoichiro Kawabe; Hideaki Fujiwara and Koyo Yanagawa GRIFFITH HACK CO.
71 YORK STREET SYDNEY NSW 2000
AUSTRALIA
Complete Specification for the invention entitled: MOLD ADDITIVE FOR CONTINUOUS CASTING OF
STEEL
The following statement is a full description of this invention, including the best method of performing it known to me/us:- 1102A:rk apsicUnt(s) sisubject of the application.
basic applicant(s).
inatureo Declared at Tokyo, Japan this 3rd day of October 19 88 declarant(). SHINAGAWA REFRACTORIES CO., LTD.
(N.B.-No seal or stamp im prcsion to be apoId). By: To TheCommissioner of Patents, aiAO Commonwealth of Australia Pr .ft GRIFFITH, HASSEL FRAZER Box 2133, G.P.O. SYDNEY 2001 AUSTRALIA 8 -64 6 i 8646 00 o 0 0 0a 00 00l 01 0 00 es a 0 1 0 00 0 0 0 04000 TITLE OF THE INVENTION: MOLD ADDITIVE FOR CONTINUOUS CASTING OF STEEL BACKGROUND OF THE INVENTION: The present invention relates to a mold additive suitable for use in a mold for continuous casting of steel and, more particularly, to a mold additive that contains synthetic calcium silicate as a base material and is suitable for use in a mold for continuous casting of steel.
Such a mold additive for use in a mold for continuous casting of steel is composed of a primary material such as portland cement, yellow phosphorus slag, or wollastonite and, as required, an SiO2-containing material. The mold additive further includes a flux material such as soda ash, borax, cryolite, sodium fluoride or fluorite, and a carbonaceous material which serves as a melting-rate adjusting agent.
The mold additive is applied to the surface of a molten steel which has been poured into a mold, in which the mold additive is consumed while performing various functions. The important functions of the mold additive are lubrication between the mold and a solidifying shell, melting and absorption of any inclusion which rises to the surface of the molten steel, and heat insulation with respect to the molten steel.
The progressive development of continuous casting processes in Japan is outstanding, and active efforts are
-A
1062A:JM being directed to increasing the proportion of HCR (hot charge rolling) or HDR (hot direct rolling) in a complete continuous casting process, the speeding up of casting, and so forth. In this situation, it is strongly desired to employ even stricter criterion for the mold additives which influence the quality of cast pieces and the stability of a casting process and, in addition, there is a demand for the supply of mold additives of various kinds which have characteristics that greatly differ from those of conventional mold additives. For these reasons, it has been proposed to provide a wide variety of chemical compositions which govern various characteristics of these mold additives, o C o such as softening point, melting point, viscosity, surface tension and crystallization temperature. In particular, it o. is of great importance to adjust the weight ratio of CaO to SSiO 2 (hereinafter referred to as the "CaO/Sio ratio") as 2 2 this ratio has a critical influence on these characteristics.
Ii To achieve the functions and among the above noted functions of such a powder, it is most important to adjust the characteristics such as a softening point and viscosity of the mold additive which invites the importance of selection of chemical composition mentioned above. To achieve the function regarding the heat insulation with respect to a molten steel, it is important to suitably select such powder characteristics as bulk density and -2- .111 _11: spreadability, as well as the powder's melting rate which can be adjusted by a carbonaceous material.
The base material of the conventional mold addtive is selected from among portland cement, yellow phosphorus slag, synthetic slag, wollastonite and the like. Each of these materials, however, has its merits and demerits, and there is no material having the characteristics to meet all the requirements of a base material.
For example, portland cement is characterized by its oa relatively stable chemical composition. Further, since its 9 S9, CaO/SiO 2 ratio is higher than those of the other base o materials, by combining the portland cement and a pearlite powder such as a light SiO 2 -containing material, it is possible to achieve low bulk density and good heat insulation a and to adjust the CaO/SiO 2 ratio over a wide range. However, o 0 portland cement contains 4CaO At3 Fe0 in a range of 9 to 15% by weight and hence the resulting mold additive S usually contains Fe 2 0 3 in an amount of about 2% by weight.
The Fe 2 0 3 in the powder may react with a component (for example, At) of a molten steel to cause contamination of the molten steel and this will at the same time result in a change in the characteristics of the mold additive.
Accordingly, it is impossible to achieve stable lubrication.
In addition, since a powder which includes portland cement as its base material is susceptible to hydration, it is difficult to subject such a powder to granulation using a generally adopted granulation process which comprises the steps of watering, k-,eading and extruding.
In contrast, yellow phosphorus slag, as well as synthetic slag having a composition analogous to that of the same, is a molten-quenched in water and crushed substance.
Accordingly, such slag can be used as an amorphous material which excels in homogeneity of component distribution, and granulation thereof is easy. However, since the CaO/SiO 2 ratio is relatively low if a mold additive having a relatively high CaO/SiO 2 ratio is to be manufactured, the amount of light SiO 2 -containing material added needs to be reduced, thus resulting in the problem that the bulk density of the obtained powder is high. Another disadvantage of this material is that a powder composition having a CaO/SiO 2 ratio of 1.15 or more cannot be obtained.
Wollastonite has an even lower CaO/SiO 2 ratio and its use is therefore limited to an extremely narrow range of applications. In addition, wollastonite is inferior in terms of the stability of its components.
Various other methods have been proposed, for example, a method of producing a powder having a high CaO/SiO 2 ratio by adding limestone or fluorite to a base material such as yellow phosphorus slag or wollastonite having a relatively low CaO/SiO 2 ratio. However, all of the conventional methods -4involve problems with respect to the stability of the product quality. Accordingly, it has been impossible to provide a powder of desired quality.
SUMMARY OF THE INVENTION: The present inventors investigated various kinds of material in order to solve the above-described problems experienced in the conventional types of powder base material and discovered that as for a base material for a mold additive of the present invention, a synthetic calcium silicate having CaO and SiO 2 in a total amount not less than 70% by weight, A203 in an amount not more than 8% by weight, S Fe203 in an amount not more than 1% by weight, and F in an i 2 3 S amount of 1 to 10% by weight, and whose CaO/SiO 2 ratio is not i2 lower than 1.20 is suitable for achievement of the object of the present invention.
SIt is, therefore, an object of the present invention to provide a mold additive suitable for use in a mold for continuous casting of steel, which mold additive includes, as its base material, at least 50% by weight of synthetic calcium silicate which contains CaO and SiO 2 in a total Samount not less than 70% by weight, AZ 2 0 3 in an amount not more than 8% by weight, Fe20 3 in an amount not more than 1% by weight, and F in an amount of 1 to 10% by weight, and whose CaO/SiO 2 ratio is not lower than 1.20.
~I I I DESCRIPTION OF THE INVENTION: Synthetic calcium silicate which is used as the base material of a mold additive according to the present invention has a relatively high CaO/SiO 2 ratio. Accordingly, if the mold additive is to be manufactured, a large amount of light SiO 2 -containing material can be employed. Therefore, it is possible to provide a mold additive having low bulk density and good heat insulation properties and also to select the CaO/SiO 2 ratio over a wide range by changing the amount of Si0 2 -containing material to be added. In addition, 42 since the Fe 2 3 content of synthetic calcium silicate is 2 3o small, the amount of AZ 2 0 3 generated due to the reaction of o Fe20 Fe 3 with AZ in a molten steel is small, so that it is possible to prevent contamination of the steel. Furthermore, the extent of change in powder characteristics due to the S generation of AZ 203 is small and thus stable lubrication is P enabled. Accordingly, the synthetic calcium silicate of the present invention possesses characteristics suitable for use as the base material of the mold additive for which an especially strict criterion must be employed.
Synthetic calcium silicate used in the present invention is easily obtained in the following manner. Materials such as CaCO 3 Ca(OH) 2 dolomite, siliceous sand, quartzite, bauxite, clay, chamotte, cullet, soda ash, lithium carbonate, cryolite, sodium fluoride, fluorite and coke powder are mixed so as to form a predetermined chemical composition, melted at a high temperature not lower than 1,4001C in a heating furnace such as an electric furnace, quenched in water and granulated, dried at 10 0 1C or higher, and ground to under 100 mesh by a conventional pulverizing mill such as a ball mill.
The coke powder is added to reduce and eliminate Fe 203 in a melt, while the glass powder is added to shorten a melting time period.
Since the synthetic calcium silicate thus obtained is an ao amorphous molten-quenched in water and crushed material, its components are distributed homogeneously and neither free CaO o S O o nor hydratable minerals such as 3CaO SiO are contained.
02 S Accordingly, the present synthetic calcium silicate can be granulated by a granulation process which comprises the steps 0 00 of watering, knealing and extruding or by spray-drying the o 00 •a same in a slurry-like form.
*sit Next, the composition of the synthetic calcium silicate base material will be described. Its CaO/SiO 2 ratio is selected to be not lower than 1.20. This is because, if the CaO/SiO 2 ratio is not lower than 1.20, the range of selection of the CaO/SiO 2 composition of a mold additive can be widened and because, if a large amount of light SiO 2 is used, a powder having low bulk specific gravity and good heat :i insulation properties can be obtained. From these viewpoints, it is preferable that the CaO/SiO 2 ratio of -7synthetic calcium silicate is as high as possible. However, as the CaO/SiO 2 ratio is increased, the solidifying point and crystallization temperature of a melt become higher and thus the manufacture of melts becomes remarkably difficult, with the result that the desired amorphous material is difficult to obtain in a stable state. Accordingly, the CaO/SiO 2 ratio of synthetic calcium silicate used in the present invention is preferably 1.2 to 2.3, more preferably 1.2 to 1.9.
The powder occasionally absorbs a large amount of At 2 0 3 which rises to the surface of a molten steel in the mold.
I If powder slag contains At 2 0 3 in an amount not less than S, by weight, a high-melting-point mineral such as gehlenite t I (2CaO At 2 0 3 2 Si is precipitated and the effect of lubrication deteriorates. Accordingly, the AZ 2 0 3 content of the synthetic calcium silicate used in the present invention is preferably not more than 8% by weight, more preferably not more Sthan 5% by weight.
Fe 2 0 3 reacts with components contained in a molten steel to cause contamination of the steel and also to cause changes is necessary to limit the Fe 2 0 3 content of the synthetic calcium silicate to not more than 1% by weight, more preferably not more than 0.3% by weight.
F is added for the purpose of adjusting the viscosity of a melt in the manufacture thereof and improving the -8efficiency of working operation. If an excessive amount of F is added, a melting furnace is damaged severly and also changes in composition due to evaporation is found. If the amount of F added is excessively small, the effect of viscosity drop will be small. Accordingly, the F content of the present synthetic calcium silicate is preferably 1 to by weight, more preferably 2 to 7% by weight.
Further, flux components such as Na20 Li 2 O and B23 are Na 2 23 added for purposes similar to those of F, so that it is possible to adjust the melting point and viscosity of a melt during manufacture of synthetic calcium silicate. However, in view of damage to a melt container or the amount of evaporation during manufacture, it is preferable that the total amount of the flux components added is not more than by weight.
The powder of the present invention is composed of a base material, a Si02-containing material, a flux material and a carbonaceous material all of which will be listed below: base material: synthetic calcium silicate SiO2-containing material: pearlite, fly ash, siliceous sand, glass powder, diatomaceous earth or the like, flux material: soda ash, Li 2 C03, NaF, Na 3 AkF 6 fluorite, BaCO 3 MgCO 3 MgF 2 t borax or the like, and carbonaceous material: coke powder, carbon black, natural graphite or the like.
It is necessary to adjust the melting characteristics of the mold additive, such as softening point, melting point, viscosity, surface tension, crystallization temperature, and melting rate in accordance with casting conditions such as casting temperature, mold size, the grade of steel and casting speed. Such melting characteristics are governed by the chemical composition of the mold additive, and the above-described materials need to be mixed so that each of a the materials may assume a predetermined chemical 0 composition.
OoO In accordance with the present invention, the chemical 1 composition of the mold additive (or powder) for use in a a 09 continuous casting of steel is as follows: o4 0 CaO 20 to 45% by weight, SiO 25 to 50% by weight, 2 the weight ratio of CaO/SiO 2 0.7 to A203 0 to 10% by weight, Fe203 0.1 to 2.0% by weight, MgO 0 to 10% by weight, Na 2 O K 2 0 Li2O 1 to 25% by weight, F 2 to 15% by weight,
B
2 0 3 0 to 10% by weight, Mn to by eight, MnO 0 to 5% by weight, and BaO 0 to 15% by weight, and C 0.5 to 10% by weight.
The mold additive having the above chemical composition according to the present invention is obtained by mixing at least 50% by weight of synthetic calcium silicate base material, 2 to 30% by weight of SiO 2 material, 3 to 30% by weight of flux material and 0.5 to 8% by weight of carbonaceous material.
It is undesirable for the amount of synthetic calcium silicate added to be less than 50% by weight, since the homogeneous distribution and stability of components which fa are characteristic of synthetic calcium silicate is lowered.
br S. The SiO2-containing material is used for the purpose of Sadjusting the bulk density and CaO/SiO ratio of the powder.
2 It is undesirable for the amount of Si0 2 -containing material Sadded to be less than 2% by weight, since the bulk density 4 cannot be sufficiently lowered even with th use of a light KSiO 2 -containing material such as pearlite and, in addition, heat insulation properties would deteriorate. Also, it is undesirable for the amount of Si 02-containing material added 2 to exceed 30% by weight, since the bulk density becomes too small and the amount of powder dust generation increases.
To adjust the melting characteristics, it is necessary to add the flux material in an amount not less than 3% by weight. However, if an excessive amount of flux material is added, its composition may change due to evaporation duringf -11- CaO 20 to 45% by weight, SiO 2 25 to 50% by weight, the weight ratio of CaO/SiO 2 0.7 to A203 0 to 10% by weight, 2 3 /2 melting and, in addition, the immersion nozzle used in pouring a molten steel into a mold may be seriously damaged.
Accordingly, it is preferable that the maximum amount of flux material added is 30% by weight.
The carbonaceous material is added in order to adjust the melting rate of the powder. If the amount of addition is less than 0.5% by weight, no substantial effect can be obtained. On the other hand, it is undesirable that the amount of addition exceeding 8% by weight, since the melting rate decreases to an excessive degree.
The mold additive according to the present inverion is obtained by preparing each of the materials in accordance with the above-described chemical composition and mixing the prepared materials in a V-type mixer or a nauter mixer. In addition, it is possible to obtain granules of columnar shape by kneading tire material mixture with water and granulating it by an extrusion granulator. It is also possible to obtain a mold additive whose grains have a spherical shape by I converting the material mixture into a slurry-like form and effecting spray-drying thereof.
1| EXAMPLE Preparation of Synthetic Calcium Silicate Base Material 1 A mixture of the materials which had the composition j shown in the following Table 1 was melted by heating at a temperature of 1,650 to 1,700°C in an electric furnace, and -12- I- i' -r 1 1 1: i the obtained melt was quenched in water and crushed. The granules were dried at 190 0 C and finally ground to under 100 mesh by a ball mill, thus preparing base materials composed of synthetic calcium silicate 1, 2 and 3.
TABLE 1 Synthetic calcium silicate by weight) 1 2 3 limestone 50.5 52.0 56.5 cullet 7.5 6.0 4 chamotte 10.5 5.0 quartzite 16.0 18.0 17.0 o dolomite 7.5 9.5 14.0 fluorite 6.5 8.0 soda ash 1.5 1.5 Scoke powder (external percentage) 3.0 3.0 Table 2 shows the compositions of the obtained synthetic calcium silicate 1, 2 and 3. Table 2 further shows the compositions of yellow phosphorus slag, synthetic slag and portland cement used in preparing comparative powder samples.
I::
-i -13- The following statement is a full description of this invention, including the best method of performing it known to me/us:- 1 102AAr TABLE 2 by weight) Si02 A 2 03 Fe 2 0 3 CaO MgO N a 2 0 F Weight ratio of CaO/Si10 2 Synthetic calcium 38.7 0 .3 48 .7 2 .2 1.5 3.5 1.26 silicate 1 Synthetic calIc iurn 36.0 2.7 0 .3 52.2 3.4 1.7 4.8 1.45 silicate 2 Synthetic calcium 31.1 1.4 0.2 56.6 4.5 2.5 2.6 1.82 silicate 3 Portland cement 22.0 6 .7 4 .1 64 .2 1.4 2 .92 Yellow phosphorus 44.0 3.0 0.2 48.5 0.3 0.4 2.5 1.10 slag Synthetic slag 43.5 3.0 0.3 48 .5 0.8 1.0 2.6 1.11
GA
o GG2 A GO C AG A 0 4 0*00 GA GA AG A C C G AG A PG A A A AG A GA AG A
A
GAGAGA
A P 00000* A A p.
AG A 0 0*
A
GA.0'~G C G Base materials composed of synthetic calcium silicate 1, 2 and 3 were each mixed with the mixtures of the materials which had the composition shown in the following Table 3 by means of a V-type mixer, thus preparing mold additive samples of the present invention and comparative mold additive samples.
The results when applied for actual casting processes as well as the compositions and typical characteristics of the respective powder samples are shown in Table 3.
-14ia .~i a a.~ a a t a4 a a.
a i aqai a, a a t a a a i a ti TABLE 3 Samples according I Comparative I to this invention ____samples 1 2 3 -4 5 6 7 8 Synthetic calcium 841 silicate 1 Synthetic calcium 57 58 silicate 2 Synthetic calcium 66 Ssilicate 3 HYellow phos- 8~phorus slag .Synthetic Sslag 0 Portland -Hcement 44 SSio Cconi~aining 25 17 13 5 25 39 -4 material X SFluorite 8 Flux material 14 13 13 10 10 13 16 18 Carboneceous material 4 4 4 1 7 4 4 4 .A.s 2 39.2 33.5 31.9 36.3 39.7 38.3 34.8 31.0 At03.4 2.7 2.7 5.6 4.9 6.1 2.4 2.1 .8Fe 2 0 3 0.2 0.2 0.2 2.0 0.2 0.2 .~Ca0 31.0 37.9 39.8 40.9 30.5 30.1 38.8 39.1 go 2.3 3.1 3 .2 1. 20 11 06 02 a
I
a ti t I i I I I
I
(continued) 12.5 11.9 11.5 8.9 9.6 12.6 12.0 11.7 S7.7 7.6 7.7 7.5 7.3 5.9 7.6 7.8 Free carbon 3.8 3.8 3.8 0.94 6.6 3.8 3.8 3.8 Weight ratio of CaO/SiO 0.79 1.13 1.25 1.13 0.77 0.79 1.11 1.26 Softening 1060 1110 1135 1130 1070 1030 1110 1140 Spoint Viscosity r (poise, 3.6 2.4 1.2 2.9 4.0 3.5 2.3 1.1 o 1300 0
C)
a SBulk density 0.75 0.78 0.77 0.79 0.73 0.72 0.97 1.01 Heat insulation Good Good Good Good Good Good Bad Bad property n Surface Rarely Frequently defect observed observed 0 SLubrication stability o o o o o x o Quality Sstability o o o o o A o x NOTE) In Table 3, SiO2-containing material: total of the weight percents of pearlite powder and glass powder, flux material: total of the weight percents of soda ash and sodium fluoride, softening point: measured by a Seger-cone method at a temperature rise of viscosity: measured by a platinum-ball lifting method, -16-
I
bulk density: a 1-k container, charging naturally, heat insulation property: by the observation of the condition in a mold, surface defect: slag spot, pinhole, longitudinal crack, etc.,
I
lubrication stability: results of mold copper temperature measurements, and quality stability: frequency of the occurrence of break-outs and surface defects.
i
I
-17- ;I a The synthetic calcium silicate base material which is used for the mold additive for a continuous casting of the present inventive powder possesses the merits of both portland cement and yellow phosphorus slag. Accordingly, the mold additive of the present invention which contains at least 50% by weight of synthetic calcium silicate provides the following features.
1) Since the light SiO 2-containing material is added, low bulk density and good heat insulation properties can be achieved.
2) If the amount of SiO 2 material to be added is adjusted, it is possible to manufacture various powders whose compositions range from a low CaO/SiO 2 ratio to a high CaO/SiO 2 ratio.
3) Since the Fe 2 0 3 content is small, stable lubrication is achieved.
4) Since neither free CaO nor 3CaO- SiO 2 is contained, granulation with water can be adopted.
All the components can be homogeneously distributed.
-18-

Claims (4)

1. A mold additive suitable for use in a mold for continuous casting of steel characterized by that said mold additive comprises, as its base material, at least by weight of synthetic calcium silicate which contains CaO and SiO 2 in a total amount not less than 70% by weight, Al203 in an amount not more than 8% by weight, Fe 2 0 3 in an amount not more than 1% by weight, and F in an amount of 1 to 10% by weight and whose CaO/SiO 2 ratio is not lower than 1.20.
2. A mold additive according to Claim 1, wherein the CaO/SiO 2 ratio of said synthetic calcium silicate is 1.2 to 2.3.
3. A mold additive according to Claim 1, wherein the CaO/SiO 2 ratio of said synthetic calcium silicate is 1.2 to 1.9.
4. A mold additive according to Claim 1, wherein the CaO/SiO 2 ratio of said synthetic calcium silicate is 1.2 to 1.9 and said synthetic calcium silicate contains Al203 in an amount not more than 5% by weight, and Fe 2 0 3 in an amount not more than 0.3% by weight. A mold additive suitable for use in a mold for continuous casting of steel, substantially as hereinbefore described with reference to any one example disclosed. Dated this 7th day of March, 1990 SHINAGAWA REFRACTORIES CO., LTD By their Patent Attorney GRIFFITH HACK CO. S -19- 7728S/CB
AU23687/88A 1987-10-19 1988-10-12 Mold additive for continuous casting of steel Ceased AU598398B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP26187987A JPH01104452A (en) 1987-10-19 1987-10-19 Additive for casting mold for continuously casting steel
JP62-261879 1987-10-19

Publications (2)

Publication Number Publication Date
AU2368788A AU2368788A (en) 1989-05-25
AU598398B2 true AU598398B2 (en) 1990-06-21

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JP (1) JPH01104452A (en)
AU (1) AU598398B2 (en)
CA (1) CA1324239C (en)
DE (1) DE3835492A1 (en)
FR (1) FR2621840B1 (en)
GB (1) GB2211178B (en)

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* Cited by examiner, † Cited by third party
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JPH0673730B2 (en) * 1990-11-30 1994-09-21 品川白煉瓦株式会社 Exothermic mold powder for continuous casting
AT404098B (en) * 1991-03-28 1998-08-25 Tisza Bela & Co METHOD FOR PRODUCING GRANULATED CONTINUOUS POWDER
CA2303825C (en) * 1998-07-21 2007-01-09 Shinagawa Refractories Co., Ltd. Molding powder for continuous casting of thin-slab
WO2011006649A1 (en) * 2009-07-14 2011-01-20 Corus Staal Bv Casting mould powder
SG11202109435YA (en) 2019-02-06 2021-09-29 Air Liquide Compound and method for producing lithium-containing film
CN119794293B (en) * 2025-01-22 2025-09-19 佛山市华儒铜业有限公司 Borax adding method and device in TP2 copper alloy continuous casting process

Citations (1)

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Publication number Priority date Publication date Assignee Title
AU592250B2 (en) * 1987-02-12 1990-01-04 Shinagawa Refractories Co., Ltd. Mould additive for continuous casting of steel

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Publication number Priority date Publication date Assignee Title
GB792023A (en) * 1955-02-21 1958-03-19 Harry Marsh Sinclair Jr Improvements in process for producing sodium fluoride from an alkaline earth fluoride
GB1230094A (en) * 1967-05-04 1971-04-28
GB1243837A (en) * 1968-11-08 1971-08-25 Inst Zuschlagstoffe Und Naturs Method of production for synthetic wollastonite
DE1912354B2 (en) * 1969-03-12 1972-04-13 Reimbold & Strick, 5000 Köln-Kalk SYNTHETIC CRYSTALLINE CALCIUM SILICATE AND THE PROCESS FOR ITS MANUFACTURING
AT320184B (en) * 1971-12-14 1975-01-27 Concast Ag Casting powder for use in the continuous casting of steel
FR2234244B1 (en) * 1973-06-20 1978-02-17 Rech Geolog Miniere
CA1147528A (en) * 1979-06-09 1983-06-07 Seikichi Tabei Additives for continuous casting of steel
DE3236391C2 (en) * 1982-10-01 1992-05-27 Hans Joachim Dipl.-Ing. Eitel Casting powder for steel casting
JPS61115653A (en) * 1984-11-09 1986-06-03 Nippon Steel Corp Continuous casting method of medium-carbon steel
US4738719A (en) * 1986-05-09 1988-04-19 Tenneco Canada Inc. (Erco Division) Steel making flux

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU592250B2 (en) * 1987-02-12 1990-01-04 Shinagawa Refractories Co., Ltd. Mould additive for continuous casting of steel

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GB2211178A (en) 1989-06-28
DE3835492A1 (en) 1989-04-27
GB2211178B (en) 1991-09-18
GB8823909D0 (en) 1988-11-16
JPH01104452A (en) 1989-04-21
AU2368788A (en) 1989-05-25
DE3835492C2 (en) 1991-06-27
FR2621840B1 (en) 1995-02-10
FR2621840A1 (en) 1989-04-21
JPH0227063B2 (en) 1990-06-14
CA1324239C (en) 1993-11-16

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