US3251680A - Method and apparatus for treating steels - Google Patents
Method and apparatus for treating steels Download PDFInfo
- Publication number
- US3251680A US3251680A US280906A US28090663A US3251680A US 3251680 A US3251680 A US 3251680A US 280906 A US280906 A US 280906A US 28090663 A US28090663 A US 28090663A US 3251680 A US3251680 A US 3251680A
- Authority
- US
- United States
- Prior art keywords
- molten metal
- ladle
- metal
- particles
- molten
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 229910000831 Steel Inorganic materials 0.000 title claims description 42
- 239000010959 steel Substances 0.000 title claims description 42
- 238000000034 method Methods 0.000 title claims description 28
- 229910052751 metal Inorganic materials 0.000 claims description 96
- 239000002184 metal Substances 0.000 claims description 96
- 239000002245 particle Substances 0.000 claims description 34
- 239000011261 inert gas Substances 0.000 claims description 2
- 238000005201 scrubbing Methods 0.000 claims description 2
- 239000011734 sodium Substances 0.000 description 27
- 229910052708 sodium Inorganic materials 0.000 description 25
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 24
- 239000002893 slag Substances 0.000 description 24
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 22
- 239000003795 chemical substances by application Substances 0.000 description 20
- 239000007789 gas Substances 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 229910052786 argon Inorganic materials 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 238000002347 injection Methods 0.000 description 10
- 239000007924 injection Substances 0.000 description 10
- 239000003638 chemical reducing agent Substances 0.000 description 8
- 229940124024 weight reducing agent Drugs 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 230000001603 reducing effect Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 238000013019 agitation Methods 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000012535 impurity Substances 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 238000007872 degassing Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 3
- 229910052684 Cerium Inorganic materials 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 2
- 229910001634 calcium fluoride Inorganic materials 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052681 coesite Inorganic materials 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229910052906 cristobalite Inorganic materials 0.000 description 2
- 230000001627 detrimental effect Effects 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910052682 stishovite Inorganic materials 0.000 description 2
- 229910052905 tridymite Inorganic materials 0.000 description 2
- KPZGRMZPZLOPBS-UHFFFAOYSA-N 1,3-dichloro-2,2-bis(chloromethyl)propane Chemical compound ClCC(CCl)(CCl)CCl KPZGRMZPZLOPBS-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000519 Ferrosilicon Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 241000272534 Struthio camelus Species 0.000 description 1
- PWKWDCOTNGQLID-UHFFFAOYSA-N [N].[Ar] Chemical compound [N].[Ar] PWKWDCOTNGQLID-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 230000005674 electromagnetic induction Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 150000004673 fluoride salts Chemical class 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Inorganic materials [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 1
- -1 magnesiumQsilic'on Chemical compound 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000012629 purifying agent Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- MNWBNISUBARLIT-UHFFFAOYSA-N sodium cyanide Chemical compound [Na+].N#[C-] MNWBNISUBARLIT-UHFFFAOYSA-N 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000004763 sulfides Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21C—PROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
- C21C7/00—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00
- C21C7/0037—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00 by injecting powdered material
- C21C7/0043—Treating molten ferrous alloys, e.g. steel, not covered by groups C21C1/00 - C21C5/00 by injecting powdered material into the falling stream of molten metal
Definitions
- a method of removing unmelted foreign matters ineluded in .the Imolten metal generally considered adoptable for industrial use is iiltering. Those with diierent speciic gravities :from the metal may be removed by use of the centrifugal ⁇ or centripetal force. There have been diicullties, however, preventing these methods from being satisfactorily adopted in removing foreign matters, such as non-metallic inclusions, etc., from the molten metal, and, therefore, they are not generally in use.
- the main feature of this invention is to disintegrate the stream or molten metal into numerous minute particles by means of a gaseous body or la body of gas containing addition agents, and to let these particles of molten metal pass through the layer of lthe slag.
- the method of this invention may be applied profitably to -all kinds or molten alloy with iron kas their main ingredient.
- This invention may be applied to every kind of molten metal stream, whatever be the case, as, for example, to that poured from the nozzle in-to casting molds or to similar molten metal stream or to metal stream being tapped fro-m the molten metal in the furnace.
- the pressure to be applied to the lmolten metal stream may be either increased or decreased in compliance with the particular needs .ot it, and thus t-o obtain advantageous conditions for improving yield, etc., by maximum stream disintegration.
- the Imolten metal may be held in va ladle of an approprivate shape equipped with one or more nozzles, through which it may be re-poured.
- These gaseous bodies have the function of deoxi- 1 dation prevention of oxidation, degassing', and gaseous ingredient addition, besides functioning as carrier media for other agents.
- the gaseous body used in connection with the molten metal -stream is regulated at proper speed, angle .and quantity. As occasion may require, it mayl be -used in confluence with the molte-n metal stream. In either case,
- the speed of the current and the volume of lgaseous body may be increased.
- the angle of injection of the gaseous body into the molten metal stream is to .be so arranged that the current of the gas may have the maximum relative speed aga-inst the movement of the molten metal stream.
- the disintegrated molten steel is further filtered through the layer of the slag, which is described below.
- Injection is made, in accordance with the requirement, with pure gaseous body alone or gas mixed with deoxidizing, desulphurizing, purifying, heat generating, heat absorbing, degassing agents and ingredients addition, either separately or some or all of them together either in the form of solid or liquid.
- the injection of the aforesaid agents and ingredients addition may also be4 made separately. All such injections, moreover, are made into a closed or open box equipped with an exhaust for gas.
- Effective results may be achieved by adding in advance the above-mentioned deoxidizing, desulphurizing, purifying,l ingredients addition, and heat generating agents in the aforementioned ladle or re-poured vessel.
- Slag which is used to filter the molten metal under the method claimed by this invention, is made to form in the ladle or in the repoured vessel by adding the molten slag, or by transferring the slag melted in advance in another container, or may be formed on top of the molten metal by adding the slag-forming agent separately.
- Disintegrated particles of the molten metal are filtere through this layer of the slag.
- deoxidizing agents such as hydrogen gas or metals such as Na, Mg, ⁇
- Desulphurization agents used in this invention are fluorides such as NaF or CaF2, chlorides, oxides such as CaO, and metals such as Mg, Ca, Na and Ce, either independently or in the form of a mixture, and may be added in the same manner as in the case of deoxidizing agents in order to attain effective desulphurization. Desulphurization may be made particularly effective when done within the reducing atmosphere as in the case of deoxidation.
- the purifying agents to be used in connection with this invention are the aforementioned slag-forming agents, which are selected for better fluidity at operating temperature.
- Slag-forming agents added by the aforementioned method (and the slag which is formed by adding the other addition agents) float up on top ofthe molten metal in the melted state and form the slag layer of predetermined required viscosity.
- Another point of this invention is that although steels generally contain such harmful gases as hydrogen, nitrogen etc., these gases may easily be reduced by making the molten steel into the form of minute particles and at the same time reducing the partial pressure of the elements in the atmosphere.
- this invention makes it possible to effectively purify the steel by deoxidation, ⁇ desulphurization, degassing, removal of non-metallic inclusions, achieved either independently or simultaneously, by means of ltering the finely disintegrated particles of molten steel through the slag, and selecting and controlling the gaseous body used in order to disintegrate the molten steel into fine particles.
- addition gaseous body to be used as addition agents for the purposes of deoxidation, desulphurization, degassing and filtering may be easily con- -trolled and also addition agents can easily combine with gaseous body to give effective performances.
- addition ingredients can easily be mixed which makes it possible to easily attain uniform distribution of ingredients even with steels containing many addition ingredients.
- any of the following methods may be used: electromagnetic induction agitation, placing the ladle on an eccentric turn-table, mechanical agitation, etc., depending upon the respective circumstances.
- the molten metal thus processed by the methods covered in this invention is to be poured into the casting molds, etc., by operating the stopper.
- FIG. 1 is a cross section of an apparatus equipped with a tundish-type molten metal container above the ladle provided with an induction agitation device.
- FIG. 2 is a cross section of an ordinary ladle, equipped with a device to introduce the jet stream to be used for re-ladling in accordance with this invention.
- FIG. 3 is a diagram illustrating the effect of dispersing a molten stream of metal into droplets.
- FIG. 1 shows a ladle 1 covered with a shallow tundish-type molten metal container 3 and 3 substantially the same diameter as the ladle 1 and with a single or a plurality of nozzles 4 at the bottom,
- the invention is not limited to a particular location for these nozzles 4.
- the molten metal stream 5 inthe tundish 3 streams through the nozzle 4 of the molten metal container 3 and 3 and ⁇ then down to the ladle 1. At this point, molten metal stream 5 is disintegrated into ⁇ a cloud of fine particles by a gaseous body 7 jetted lout from nozzles of pipes 6 equipped at the side of the molten metal container 3.
- the flux is melted and floats up above the molten metal 8 in the ladle 1 and forms a slag layer 9.
- the disintegrated particles of the molten metal are filtered when passing through the layer of the slag 9 kand non-metallic inclusions are removed.
- neutral or reducible gas may be used as the gaseous body 7 so that the ⁇ atmosphere within the ladle 1 may be easily controlled.
- the injected gaseous body 7 is exhausted through a hole 12 cut through a portion of the lower part 3 of the molten metal container 3'. This hole is positioned at the arm 14 used to attach the stopper 13 when the molten metal container 3 is placed on top of the laddle 1.
- the molten metal may be introduced in a stream directly from a furnace (not shown) or from a ladle 15.
- Apparatus 16 is provided for adding addition agents not introduced through the pipes 6.
- the molten metal is tapped from a 20D-ton basic openhearth furnace and pre-deoxidized.
- One hundred tons of the molten metal with the following chemical composition is poured into the laddle 15:
- Percent Ferro-silicon is added to the molten metal within the molten metal container 3' by means of the adding apparatus 16 raising its Si content to 1.2%.
- the molten metal then is allowed to flow downward by natural gravity through 50 mm. nozzles 4 and argon gas is injected at the pressure of 5 kg./cm.2 through a 25 mm. inside diameter pipe to disintegrate the molten metal into fine particles.
- the slag is thus made to fioat up' on top of the molten metal, while the finely disintegrated particles of molten metal react and are purified by being filtered by the abovementioned slag.
- the final composition of the molten metal is found to be as follows:
- the ratio of desulphurization has been found to be 45% and the non-metallic inclusions have been found to show the following reduction in comparison to the steel not treated by the method of this invention:
- This invention may also be practiced by using the apparatus shown in FIG. 2, using a ladle with a nozzle 11 discharging into the ladle 1.
- the same effect as performing re-ladling twice may be attained by performing the re-ladling only once, thus contributing to the simplification of the operations.
- the molten metal 8 inthe casing ladle 1 can easily be made of uniform -composition by Vadding the addition alloys to its surface in the container 3 by means of the adding apparatus 16.
- the induction coil 2 may be used also for heating the ladle 1 and maintaining the metal 8 molten in case any reaction tends to be endothermic.
- each droplet of molten metal as it issues from the nozzle 4 of FIG. 1 tends to be an elongated form.
- the molten metal has agents introduced through the pipes 6 and issuing as the finely dispersed particles in the gaseous spray 7.
- FIG. 3b If sodium vapor is used as the reducing agent, the effect is illustrated in FIG. 3b.
- the silicon dioxide is reduced by the sodium vapor to NaSiO3
- F28 is reduced to Na2S
- nitrides and carbides are reduced to NaCN
- excess nitride are reduced to Na3N so that as is shown in FIG. 3c a droplet of pure iron emerges and falls into the ladle 1.
- the reducing agent is introduced in very finely divided form. Even when materials other than sodium are used as the reducing agent the reducing -agents are very quickly molten :by their contact with the lmolten steel because they are in such finely divided form and action takes place quickly.
- the sodium may lbe introduced by self-generated pressure from sodium tanks which are heated to vaporize the sodium and injected through the nozzles 6.
- Sodium vapor may also be injected together with nitrogen or argon or carbon monoxide, hydrogen or other reducing or inert g-as.
- Magnesium, calcium or ceriu-m may be used in the same manner as sodium. Since nitrogen is cheaper than argon nitrogen may be'employed instead of argon, the excess nitrogen merely being removed as sodiumnitride. It is significant that all the reaction products of sodium remain vaporous so that they do not -introduce impurities into the molten steel in the ladle 1.
- deoxidizers To be effective deoxidizers must have a strong 4afiinity for. oxygen, and the reaction products formed should be completely insoluble in the molten steel.
- the ideal deoxidizer would not only be insoluble, but be in the gaseous state, in the molten steel. In other words, it would form a vapor; when the deoxidizer combines with the various oxides in the molten bath.
- Aluminum while being an effective deoxidizer, forms Ian oxide, A1203 which fails to be entirely removed, since it forms a solid at the temperature of liquid steel. Some of the A1203 remains in the bath as finely dispersed particles of Al2O3, which are detrimental, in the solid steel, reducing its impact strength, ductility etc. and adversly effecting many other ⁇ physical properties.
- sodium is even more potent as a deoxidizer of steel.
- lIt I also forms an oxide Na20 which remains in vapor form at the temperature of liquid steel. In other words it will not contaminate the steel ybath with finely disperse-d particles, as in the case of aluminum, but Will pass from the bath as a gaseous oxide. This is also a rapid reaction.
- oxides in the bath as Si02, A1203, Cr203, MnO, FeO, etc. which contact fthe Na20 ⁇ as it passes through bath will for-m highly fiuid particles, which will coalesce, and rise from -the bath, Vand if they remain in the steel are of a type which are far less detrimental than the A1203.
- the method yof removing inclusions from molten steel which comprises the steps of forming a plurality of streams of molten metal ⁇ and projecting inert gas thereagainst to disintegrate the streams of metal into particles and allowing the particles to descend through a lter composed of approximately 52% CaO, 14% SiOZ, 5% MgO, 7% A1203 and 22% CaF for scrubbing out undesirable inclusions.
- a method of purifying molten steel which comprises the ⁇ steps of forming a plurality of streams of molten metal and projecting gas thereagainst to disintegrate the streams of metal into minute particles, said gas including a metallic reducing agent which is in the form of a vapor at the Itemperature of molten steel.
- the method of purifying ya metal which comprises the steps lof forming a stream of molten metal, confining sodium, raising the ltemperature of the sodium to the temperature of gasification, releasing gasied sodium in a confined path transverse to the molten metal stream and thereby projecting a stream of gaseous sodium reducinV agent against the stream of molten metal to disintegrate the stream ⁇ of metal into particles and expose the surfaces of the particles to reducing action.
- the method of purifying molten steel which comprises the steps of forming the molten steel into a plurality of fine descending streams of molten metal, melting sodium fin argon, atomizing the sodium in said argon and projecting a jet of argon and atomized sodium against each stream of molten metal to disintegrate the streams of metal into minute particles.
- a ladle a shallow tundish type cover therefor forming a shallow molten metal bath container having a plurality of metal outletnozzles therein of approximately mm. diameter for directing a plurality of fine streams of molten metal into the ladle.
- a steel treating apparatus comprising a ladle with -a closed chamber above the ladle and equipped with ya gas exhaust at the lower portion of the chamber, With a plurality of metal outlet nozzles for the molten metal to flow down through the bottom portion of the upper chamber, and a plurality of spaced gas injection nozzles at a level lbelow the nozzles for molten metal, said gas injection nozzles serving for injection of a gaseous body directed to the molten metal from a plurality of sides Within the closed chamber.
- the method of purifying molten steel which comprises the steps of forming the molten steel into a plurality of fine descending streams of ⁇ molten metal, projecting a jet of argon against each stream of molten metal to distintegrate the streams of metal into minute particles, and carrying fluid sodium in lsaid argon jets against each stream of molten metal to make intimate contact and promote reaction with the minute particles of metal.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Description
May 17, 1966 N. P. Goss ETAL METHOD AND APPARATUS FOR TREATING STEELS 2 Sheets-Sheet 1 Filed May 16, 1965 ro /W/// //./////w//// fd v gw/ l /lwM/L 5 Hf ,Hw 7 f INVENTOI25 .C 5. 5MB ,.0 SAA N 0% i @AA O @www T WW 4 TH m @www EOD 0H! NSHM/ May 17, 1966 N. P. GOSS ETAL METHOD AND APPARATUS FOR TREATING STEELS Filed May 16, 1963 v LEJ.
2 Sheets-Sheet 2 /NVEMTOQS NOQMAN D. Goss SHozo Www/Afa@ H/Deo WANNA/s ATTORNEYS.
United States Patent C) METHOD AND APPARATUS FOR TREATING STEELS Norman P. Goss, South Euclid, Ohio, and Shozo Watal This invention relates to a train of steel-treating arrangements for removing non-metallic inclusions and for economically 'achieving -desulphurization, deoxidatron, de-
gassing and composition control in order to purify steels. v
A method of removing unmelted foreign matters ineluded in .the Imolten metal generally considered adoptable for industrial use is iiltering. Those with diierent speciic gravities :from the metal may be removed by use of the centrifugal `or centripetal force. There have been diicullties, however, preventing these methods from being satisfactorily adopted in removing foreign matters, such as non-metallic inclusions, etc., from the molten metal, and, therefore, they are not generally in use. The most usual method adopted for removing these impurities is to hold still after ,tapping the relined molten metal in the ladle sufficiently long to permit the inclu-sions to float up, provided thtat the pouring temperature of the molten metal and the operation of the stopper are not adversely affected. However, as is proved by Stokes law, when the particles of these foreign matters are smaller than a certain size, they would remain in suspension and would not llo'at up even if held still in the ladle for a considerable length of time, and'would adversely affect ,the degree ot purity ot the steel. Steeldrnaking engineers have recently come to `fully recognize the fact that these minute inclusions atleet 'adverse-ly the quality of the steels particularly in relation to their kinds Iand usage, and hence the steel users also have lcorne to demand purer and cleaner steels.
Although at the contact surface of the molten metal and the slag quick reaction takes place and the metal and the slag approach equilibrium instantaneously, it takes much longer time for the reaction to progress throug out the entire 'charge and corne to equilibrium, for the reason that it must be accompanied by dilusion. The major portion of the non-metallic inclusions contained in the tap ladle is deoxidized products, which, if left undisturbed, Wou-ld ilo'at to the'surface and lform slag. Some of them, however, are distributed in extremely small particles and are in -a colloidal state.
This invention has been made to develop advantageous and unique method `avoiding the aforementioned detects. In .other words, the main feature of this invention is to disintegrate the stream or molten metal into numerous minute particles by means of a gaseous body or la body of gas containing addition agents, and to let these particles of molten metal pass through the layer of lthe slag.
The method of this invention may be applied profitably to -all kinds or molten alloy with iron kas their main ingredient. Application to steels with many element addiltions, su-ch as to k-illed steels and .semi-killed ste-els i-s especially advantageous.
This invention may be applied to every kind of molten metal stream, whatever be the case, as, for example, to that poured from the nozzle in-to casting molds or to similar molten metal stream or to metal stream being tapped fro-m the molten metal in the furnace.
The pressure to be applied to the lmolten metal stream may be either increased or decreased in compliance with the particular needs .ot it, and thus t-o obtain advantageous conditions for improving yield, etc., by maximum stream disintegration.
3,Z5l,680 Patented May 17, 1966 The Imolten metal may be held in va ladle of an approprivate shape equipped with one or more nozzles, through which it may be re-poured.
The gaseous body, used to disintegrate such molten meta'l stream into numerous minute, highly dispersed particles comprises argon, hydrogen, nitrogen, sodium vapor, carbon monoxide, coke gas, canbon tetrachloride, and other compounds which are gasied lat t-he tempera-ture ot usage, used either independently or in combination in accordance with the requirements of the specic operation. These gaseous bodies have the function of deoxi- 1 dation prevention of oxidation, degassing', and gaseous ingredient addition, besides functioning as carrier media for other agents.
The gaseous body used in connection with the molten metal -stream is regulated at proper speed, angle .and quantity. As occasion may require, it mayl be -used in confluence with the molte-n metal stream. In either case,
it is used tocreate conditions conducive the disintegration `ot rthe molten metal stream into a system of highly dispersed minute particles.
The rfaster the speed of .the current of gaseous body applied to the molten .metal stream, the faster 'will be theA disintegration process of the latter and the more highly will they be dispersed. For langer volume of the molten metal stream, the speed of the current and the volume of lgaseous body may be increased. The angle of injection of the gaseous body into the molten metal stream is to .be so arranged that the current of the gas may have the maximum relative speed aga-inst the movement of the molten metal stream. It Iis also desirable to arrange the ladle creating a 'high speed rotation of air stream 'within it, and thus improve the eifect of dispersion, while, at the same time, causing the rotation movement of the slag and molten metal to improve the effect of purification with the 'action of agitation. It is desirable to'halve the surface areas ot disintegrated molten steel particles as lange as possible. For this purpose, gaseous body is blown against the molten metal stream in order to disintegrate it into minute particles.
The disintegrated molten steel is further filtered through the layer of the slag, which is described below.
Injection is made, in accordance with the requirement, with pure gaseous body alone or gas mixed with deoxidizing, desulphurizing, purifying, heat generating, heat absorbing, degassing agents and ingredients addition, either separately or some or all of them together either in the form of solid or liquid. The injection of the aforesaid agents and ingredients addition may also be4 made separately. All such injections, moreover, are made into a closed or open box equipped with an exhaust for gas.
Effective results may be achieved by adding in advance the above-mentioned deoxidizing, desulphurizing, purifying,l ingredients addition, and heat generating agents in the aforementioned ladle or re-poured vessel.
Slag, which is used to filter the molten metal under the method claimed by this invention, is made to form in the ladle or in the repoured vessel by adding the molten slag, or by transferring the slag melted in advance in another container, or may be formed on top of the molten metal by adding the slag-forming agent separately. 4
3 Disintegrated particles of the molten metal are filtere through this layer of the slag.
In carrying out the invention deoxidizing agents are added, such as hydrogen gas or metals such as Na, Mg,`
Si, Al, Ca, etc., or some or all of their compounds, as described before, to the re-poured vessel, molten metal stream, gaseous body for disintegration of the molten metal, or the ladle.
Especially if reducing gaseous body is used in order to disintegrate the molten metal, since the reducing agents may be added in the -reducing at-mosphere, good yield of reducing agents and effective deoxidation may be achieved.
Desulphurization agents used in this invention are fluorides such as NaF or CaF2, chlorides, oxides such as CaO, and metals such as Mg, Ca, Na and Ce, either independently or in the form of a mixture, and may be added in the same manner as in the case of deoxidizing agents in order to attain effective desulphurization. Desulphurization may be made particularly effective when done within the reducing atmosphere as in the case of deoxidation.
The purifying agents to be used in connection with this invention are the aforementioned slag-forming agents, which are selected for better fluidity at operating temperature.
Slag-forming agents added by the aforementioned method (and the slag which is formed by adding the other addition agents) float up on top ofthe molten metal in the melted state and form the slag layer of predetermined required viscosity.
When the finely disintegrated particles of the molten steel pass through this slag layer, desulphurization is easily achieved; and, furthermore, because the chances of contact between non-metallic inclusions and the slag are increased, and since non-metallic inclusions combine with the slag, it functions at filtering mechanism, and non-metallic inclusions are removed effectively.
Another point of this invention is that although steels generally contain such harmful gases as hydrogen, nitrogen etc., these gases may easily be reduced by making the molten steel into the form of minute particles and at the same time reducing the partial pressure of the elements in the atmosphere.
The method covered by this invention, for the reason that it makes it possible to select and control the gas injection in turn makes the operation easy and effective.
As described hereinafter, this invention makes it possible to effectively purify the steel by deoxidation,` desulphurization, degassing, removal of non-metallic inclusions, achieved either independently or simultaneously, by means of ltering the finely disintegrated particles of molten steel through the slag, and selecting and controlling the gaseous body used in order to disintegrate the molten steel into fine particles.
In other words, the addition gaseous body to be used as addition agents for the purposes of deoxidation, desulphurization, degassing and filtering, may be easily con- -trolled and also addition agents can easily combine with gaseous body to give effective performances.
Furthermore, in this invention, for the reasons that the molten metal moves in the form of finely disintegrated form, addition ingredients can easily be mixed which makes it possible to easily attain uniform distribution of ingredients even with steels containing many addition ingredients.
In this invention, it may sometimes be desirable to agitate the molten metal contained in the ladle, and for this purpose any of the following methods may be used: electromagnetic induction agitation, placing the ladle on an eccentric turn-table, mechanical agitation, etc., depending upon the respective circumstances.
The molten metal thus processed by the methods covered in this invention is to be poured into the casting molds, etc., by operating the stopper.
This invention will be explained by citing an actual operational example.
The accompanying drawings show some of the apparatus that is used in connection with this invention. FIG. 1 is a cross section of an apparatus equipped with a tundish-type molten metal container above the ladle provided with an induction agitation device. FIG. 2 is a cross section of an ordinary ladle, equipped with a device to introduce the jet stream to be used for re-ladling in accordance with this invention. FIG. 3 is a diagram illustrating the effect of dispersing a molten stream of metal into droplets.
As shown in FIGS. 1 and 2, either a ladle 1 equipped with the coil 2 for inducting agitation, or the usual ladle without the coil 2 is used. FIG. 1 shows a ladle 1 covered with a shallow tundish-type molten metal container 3 and 3 substantially the same diameter as the ladle 1 and with a single or a plurality of nozzles 4 at the bottom,
The invention is not limited to a particular location for these nozzles 4.
The molten metal stream 5 inthe tundish 3 streams through the nozzle 4 of the molten metal container 3 and 3 and `then down to the ladle 1. At this point, molten metal stream 5 is disintegrated into `a cloud of fine particles by a gaseous body 7 jetted lout from nozzles of pipes 6 equipped at the side of the molten metal container 3.
On the other hand, either slag is placed in the ladle 1 in advance, or flux is mixed in the gaseous body projected through the pipes 6.
The flux is melted and floats up above the molten metal 8 in the ladle 1 and forms a slag layer 9. The disintegrated particles of the molten metal are filtered when passing through the layer of the slag 9 kand non-metallic inclusions are removed.
The enclosure of the space Within which the distintegration takes place by the cover 3, such as explained in above, prevents oxidation of the finely disintegrated particles of molten metal.
To achieve such effect, neutral or reducible gas may be used as the gaseous body 7 so that the `atmosphere within the ladle 1 may be easily controlled.
The injected gaseous body 7 is exhausted through a hole 12 cut through a portion of the lower part 3 of the molten metal container 3'. This hole is positioned at the arm 14 used to attach the stopper 13 when the molten metal container 3 is placed on top of the laddle 1.
The molten metal may be introduced in a stream directly from a furnace (not shown) or from a ladle 15. Apparatus 16 is provided for adding addition agents not introduced through the pipes 6.
The molten metal is tapped from a 20D-ton basic openhearth furnace and pre-deoxidized. One hundred tons of the molten metal with the following chemical composition is poured into the laddle 15:
Percent Ferro-silicon is added to the molten metal within the molten metal container 3' by means of the adding apparatus 16 raising its Si content to 1.2%.
The molten metal then is allowed to flow downward by natural gravity through 50 mm. nozzles 4 and argon gas is injected at the pressure of 5 kg./cm.2 through a 25 mm. inside diameter pipe to disintegrate the molten metal into fine particles.
1.850 tons of slag forming agents in powder form with the following' composition is placed in the ladle 1 in ad- Vance:
The slag is thus made to fioat up' on top of the molten metal, while the finely disintegrated particles of molten metal react and are purified by being filtered by the abovementioned slag. The final composition of the molten metal is found to be as follows:
. y Percent C 0.033
Si 1.32 Mn 0.30
The ratio of desulphurization has been found to be 45% and the non-metallic inclusions have been found to show the following reduction in comparison to the steel not treated by the method of this invention:
Percent SiO2 Approximately 65 A1203 Approximately 45 Since the gas is injected under pressure and contains in said gaseous streams other agents Such as sodium, magnesiumQsilic'on, calcium, cerium, lithium, sodium or calcium fluoride, and so forth intimate mixing is achieved between these agents and the highly dispersed stream of metal. Reaction will therefore occur very rapidly due to the high increase of internal surface. These conditions favor high rate of reaction and will be completed even before the dispersed particles reach the filter slag. It is well known that due to surface tensions inclusion within the liquid particle will tend to be squeezed to the surface so will the lotherimpurities. The purification of the particles occur in the atmosphere filled with sodium vapor for example or the like and it will pass through the highly reactive filter slag thereby rubbing off the inclusion and so forth.
This invention may also be practiced by using the apparatus shown in FIG. 2, using a ladle with a nozzle 11 discharging into the ladle 1.
Also, in case re-ladling is to be performed, by using the molten metal container of the tundish-type 3 and 3' as shown'in FIG. 1, the same effect as performing re-ladling twice may be attained by performing the re-ladling only once, thus contributing to the simplification of the operations. The molten metal 8 inthe casing ladle 1 can easily be made of uniform -composition by Vadding the addition alloys to its surface in the container 3 by means of the adding apparatus 16.
The induction coil 2 may be used also for heating the ladle 1 and maintaining the metal 8 molten in case any reaction tends to be endothermic.
It will be understood that in the usual metal smelting process air or oxygen is introduced for the purpose of removing impurities such as carbon, silicon or phosphorus; but after a point the effectiveness of the process diminishes because of the small portion of impurities left and oxides remaining in the metal become objectionable. The efficiency of the present invention in removing such oxide inclusions and also sulphides is illustrated in FIG. 3. As shown in FIG. 3a, each droplet of molten metal as it issues from the nozzle 4 of FIG. 1 tends to be an elongated form. However, since the molten metal has agents introduced through the pipes 6 and issuing as the finely dispersed particles in the gaseous spray 7.
If sodium vapor is used as the reducing agent, the effect is illustrated in FIG. 3b. The silicon dioxide is reduced by the sodium vapor to NaSiO3, F28 is reduced to Na2S, nitrides and carbides are reduced to NaCN and excess nitride are reduced to Na3N so that as is shown in FIG. 3c a droplet of pure iron emerges and falls into the ladle 1. These reactions take place very rapidly because the droplets are very minute. The reducing agent is introduced in very finely divided form. Even when materials other than sodium are used as the reducing agent the reducing -agents are very quickly molten :by their contact with the lmolten steel because they are in such finely divided form and action takes place quickly.
The sodium may lbe introduced by self-generated pressure from sodium tanks which are heated to vaporize the sodium and injected through the nozzles 6. Sodium vapor may also be injected together with nitrogen or argon or carbon monoxide, hydrogen or other reducing or inert g-as. Magnesium, calcium or ceriu-m may be used in the same manner as sodium. Since nitrogen is cheaper than argon nitrogen may be'employed instead of argon, the excess nitrogen merely being removed as sodiumnitride. It is significant that all the reaction products of sodium remain vaporous so that they do not -introduce impurities into the molten steel in the ladle 1.
The Imethod describedproduces the -highest possible dispersion of the molten steel. This tremendously increases the effective internal surface of the molten metal by breaking it up into countless particles and lby bringing the impurities to the surface of each of these particles so that the area over which the chemical-reaction of -purification and reduction may take place is tremendously increased, thus making the reaction substantially instantaneous and taking place while the droplets are drifting downward and before they have coalesced into the molten mass 8.
To be effective deoxidizers must have a strong 4afiinity for. oxygen, and the reaction products formed should be completely insoluble in the molten steel. The ideal deoxidizer would not only be insoluble, but be in the gaseous state, in the molten steel. In other words, it would form a vapor; when the deoxidizer combines with the various oxides in the molten bath. Aluminum while being an effective deoxidizer, forms Ian oxide, A1203 which fails to be entirely removed, since it forms a solid at the temperature of liquid steel. Some of the A1203 remains in the bath as finely dispersed particles of Al2O3, which are detrimental, in the solid steel, reducing its impact strength, ductility etc. and adversly effecting many other` physical properties.
0n the other hand, sodium is even more potent as a deoxidizer of steel. lIt Ialso forms an oxide Na20 which remains in vapor form at the temperature of liquid steel. In other words it will not contaminate the steel ybath with finely disperse-d particles, as in the case of aluminum, but Will pass from the bath as a gaseous oxide. This is also a rapid reaction. Such oxides in the bath as Si02, A1203, Cr203, MnO, FeO, etc. which contact fthe Na20` as it passes through bath will for-m highly fiuid particles, which will coalesce, and rise from -the bath, Vand if they remain in the steel are of a type which are far less detrimental than the A1203. No one has 'heretofore worked out a satisfactory way to inject sodium into the -bath safely and effectively and by a low cost practical method. This has now been achieved, by injection with argon, CO, nitrogen, H2 or even the self-injection of Na vapor.
While the invention has been described as embodied in concrete form and as operating in a specific manner in accordance with the lprovisions of the patent statutes, it should lbe understood that the invention is not limited thereto, since various modifications will suggest themselves to those skilled in the art without departing from the spirit of the invention.
What is claimed is:
1. The method yof removing inclusions from molten steel which comprises the steps of forming a plurality of streams of molten metal `and projecting inert gas thereagainst to disintegrate the streams of metal into particles and allowing the particles to descend through a lter composed of approximately 52% CaO, 14% SiOZ, 5% MgO, 7% A1203 and 22% CaF for scrubbing out undesirable inclusions. v
2. The method of claim 1 wherein the dispersion and filtering are carried out in an enclosed chamber for forming a highly dispersed cloud of metal and preventing air from contacting the cloud of metal.
3. A method of purifying molten steel which comprises the `steps of forming a plurality of streams of molten metal and projecting gas thereagainst to disintegrate the streams of metal into minute particles, said gas including a metallic reducing agent which is in the form of a vapor at the Itemperature of molten steel.
4. The method of claim 3 wherein the metallic reducing -agent is selected from the group consisting of sodium, and cerium.
5. The method of claim 3 wherein the reducing gaseous metal is mixed with a gas selected from the group consisting of argon, nitrogen, carbon monoxide .and hydrogen.
6. The method of purifying ya metal which comprises the steps lof forming a stream of molten metal, confining sodium, raising the ltemperature of the sodium to the temperature of gasification, releasing gasied sodium in a confined path transverse to the molten metal stream and thereby projecting a stream of gaseous sodium reducinV agent against the stream of molten metal to disintegrate the stream `of metal into particles and expose the surfaces of the particles to reducing action.
7. The method of purifying molten steel which comprises the steps of forming the molten steel into a plurality of fine descending streams of molten metal, melting sodium fin argon, atomizing the sodium in said argon and projecting a jet of argon and atomized sodium against each stream of molten metal to disintegrate the streams of metal into minute particles.
8. In combination, a ladle, a shallow tundish type cover therefor forming a shallow molten metal bath container having a plurality of metal outletnozzles therein of approximately mm. diameter for directing a plurality of fine streams of molten metal into the ladle.
9. A steel treating apparatus comprising a ladle with -a closed chamber above the ladle and equipped with ya gas exhaust at the lower portion of the chamber, With a plurality of metal outlet nozzles for the molten metal to flow down through the bottom portion of the upper chamber, and a plurality of spaced gas injection nozzles at a level lbelow the nozzles for molten metal, said gas injection nozzles serving for injection of a gaseous body directed to the molten metal from a plurality of sides Within the closed chamber.
10. The method of purifying molten steel which comprises the steps of forming the molten steel into a plurality of fine descending streams of`molten metal, projecting a jet of argon against each stream of molten metal to distintegrate the streams of metal into minute particles, and carrying fluid sodium in lsaid argon jets against each stream of molten metal to make intimate contact and promote reaction with the minute particles of metal.
References Cited by the Examiner UNITED STATES PATENTS 336,439 2/1886 Samuel 75-51 645,205 3/ 1900 Hawkins 75-55 949,474 2/ 1910 Hawkins et al. 75-61 2,068,785 1/1937 Bain et al. 75-12 2,097,344 10/1937 Rohn 75-12 2,243,514 5/ 1941 Tige-rschiold 75-12 2,253,421 8/1941 De Mare 75-13 2,915,386 12/1959 Strauss 75-57 2,979,393 4/1961 Heuer 75-51 2,997,384 8/1961 Feichtinger 75-59 BENJAMIN HENKIN, Primary Examiner.
Claims (2)
1. THE METHOD OF REMOVING INCLUSIONS FROM MOLTEN STEEL WHICH COMPRISES THE STEPS OF FORMING A PLURALITY OF STREAMS OF MOLTEN METAL AND PROJECTING INERT GAS THEREAGAINST TO DISINTEGRATE THE STREAMS OF METAL INTO PARTICLES AND ALLOWING THE PARTICLES TO DESCEND THROUGH A FILTER COMPOSED OF APPROXIMATELY 52% CAO, 14% SIO2, 5% MGO, 7% AL2O3 AND 22% CAF FOR SCRUBBING OUT UNDESIRABLE INCLUSIONS.
8. IN COMBINATION, A LADLE, A SHALLOW TUNDISH TYPE COVER THEREFOR FORMING A SHALLOW MOLTEN METAL BATH CONTAINER HAVING A PLURALITY OF METAL OUTLET NOZZLES THEREIN OF APPROXIMATELY 50 MM. DIAMETER FOR DIRECTING A PLURALITY OF FINE STREAMS OF MOLTEN METAL INTO THE LADLE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3641462 | 1962-08-23 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3251680A true US3251680A (en) | 1966-05-17 |
Family
ID=12469153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US280906A Expired - Lifetime US3251680A (en) | 1962-08-23 | 1963-05-16 | Method and apparatus for treating steels |
Country Status (1)
Country | Link |
---|---|
US (1) | US3251680A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3511641A (en) * | 1965-08-14 | 1970-05-12 | Standard Messo Duisburg | Method of heating up and initiating metallurgical reactions in the pouring jet when degasifying the latter in a vacuum |
US3554521A (en) * | 1966-05-23 | 1971-01-12 | British Iron Steel Research | The treating or refining of metal |
US3639117A (en) * | 1970-05-14 | 1972-02-01 | Bethlehem Steel Corp | Method for producing bearing grade alloy steels |
US3771999A (en) * | 1970-12-03 | 1973-11-13 | Republic Steel Corp | Slag-making methods and materials |
US3778250A (en) * | 1969-02-26 | 1973-12-11 | Jones & Laughlin Steel Corp | Method for treating metallic melts |
US3837842A (en) * | 1971-08-02 | 1974-09-24 | Sumitomo Metal Ind | A method for projecting pieces of a deoxidizing agent into molten steel |
US3928022A (en) * | 1972-06-15 | 1975-12-23 | Bonvarite | Method of producing ferrous metal of constant properties from heterogeneous mixtures |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US336439A (en) * | 1886-02-16 | Edward samuel | ||
US645205A (en) * | 1899-05-06 | 1900-03-13 | Thomas A E Weadock | Process of refining iron. |
US949474A (en) * | 1906-05-21 | 1910-02-15 | Globe Steel Filtration Process Company | Process of refining iron. |
US2068785A (en) * | 1933-11-20 | 1937-01-26 | United States Steel Corp | Method of manufacturing low carbon steel |
US2097344A (en) * | 1932-12-06 | 1937-10-26 | Heraeus Vacuumschmelze Ag | Metallurgical slag reaction |
US2243514A (en) * | 1938-01-24 | 1941-05-27 | Tigerschiold Kjell Magnus | Desulphurization of cast iron |
US2253421A (en) * | 1938-09-20 | 1941-08-19 | Mare Baltzar E L De | Method and apparatus for deoxidizing and degasifying liquid steel |
US2915386A (en) * | 1955-01-24 | 1959-12-01 | Vanadium Corp Of America | Device for supplying treating agents sequentially to molten metal |
US2979393A (en) * | 1958-10-02 | 1961-04-11 | Jr Russell Pearce Heuer | Process of desulfurizing pig iron |
US2997384A (en) * | 1958-03-28 | 1961-08-22 | Fischer Ag Georg | Method of treating molten metal |
-
1963
- 1963-05-16 US US280906A patent/US3251680A/en not_active Expired - Lifetime
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US336439A (en) * | 1886-02-16 | Edward samuel | ||
US645205A (en) * | 1899-05-06 | 1900-03-13 | Thomas A E Weadock | Process of refining iron. |
US949474A (en) * | 1906-05-21 | 1910-02-15 | Globe Steel Filtration Process Company | Process of refining iron. |
US2097344A (en) * | 1932-12-06 | 1937-10-26 | Heraeus Vacuumschmelze Ag | Metallurgical slag reaction |
US2068785A (en) * | 1933-11-20 | 1937-01-26 | United States Steel Corp | Method of manufacturing low carbon steel |
US2243514A (en) * | 1938-01-24 | 1941-05-27 | Tigerschiold Kjell Magnus | Desulphurization of cast iron |
US2253421A (en) * | 1938-09-20 | 1941-08-19 | Mare Baltzar E L De | Method and apparatus for deoxidizing and degasifying liquid steel |
US2915386A (en) * | 1955-01-24 | 1959-12-01 | Vanadium Corp Of America | Device for supplying treating agents sequentially to molten metal |
US2997384A (en) * | 1958-03-28 | 1961-08-22 | Fischer Ag Georg | Method of treating molten metal |
US2979393A (en) * | 1958-10-02 | 1961-04-11 | Jr Russell Pearce Heuer | Process of desulfurizing pig iron |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3511641A (en) * | 1965-08-14 | 1970-05-12 | Standard Messo Duisburg | Method of heating up and initiating metallurgical reactions in the pouring jet when degasifying the latter in a vacuum |
US3554521A (en) * | 1966-05-23 | 1971-01-12 | British Iron Steel Research | The treating or refining of metal |
US3778250A (en) * | 1969-02-26 | 1973-12-11 | Jones & Laughlin Steel Corp | Method for treating metallic melts |
US3639117A (en) * | 1970-05-14 | 1972-02-01 | Bethlehem Steel Corp | Method for producing bearing grade alloy steels |
US3771999A (en) * | 1970-12-03 | 1973-11-13 | Republic Steel Corp | Slag-making methods and materials |
US3837842A (en) * | 1971-08-02 | 1974-09-24 | Sumitomo Metal Ind | A method for projecting pieces of a deoxidizing agent into molten steel |
US3928022A (en) * | 1972-06-15 | 1975-12-23 | Bonvarite | Method of producing ferrous metal of constant properties from heterogeneous mixtures |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Lange | Thermodynamic and kinetic aspects of secondary steelmaking processes | |
Holappa et al. | Secondary steelmaking | |
US4036635A (en) | Process for making a steel melt for continuous casting | |
KR101018535B1 (en) | Refining ferroalloys | |
KR100227252B1 (en) | Method of refining molten metal | |
Cramb | High purity, low residual, and clean steels | |
US3251680A (en) | Method and apparatus for treating steels | |
JPS59133314A (en) | Steel refinement and device in metallurgical vessel | |
US4009024A (en) | Process for regeneration and reuse of steelmaking slag | |
US2950186A (en) | Method for top blowing pulverulent burnt lime and oxygen into cast iron for refining same | |
US3897244A (en) | Method for refining iron-base metal | |
RU2231559C1 (en) | Direct method for alloying steel with complex of elements | |
Lachmund et al. | Thermodynamic and kinetic aspects of the desulphurisation reaction in secondary metallurgy | |
KR20140053195A (en) | Method and apparatus for dephosphorising liquid hot metal such as liquid blast furnace iron | |
Chakrabarti | Steel making | |
RU2201458C1 (en) | Method of modification of steel | |
US2958597A (en) | Manufacture of steel | |
RU2095429C1 (en) | Method of producing roller-bearing steel | |
US4681625A (en) | Methods for simultaneously desulfurizing and degassing steels | |
Holappa et al. | Slag Formation—Thermodynamic and kinetic aspects and mechanisms | |
RU2192482C2 (en) | Method of steelmaking | |
SU829679A1 (en) | Device for cast iron desulfurizing | |
RU2044063C1 (en) | Method for making low-alloyed steel with niobium | |
JP3465801B2 (en) | Method for refining molten Fe-Ni alloy | |
JPH0254715A (en) | Method for treating degassing in molten steel |