US3271139A - Process for the production of low sulfur ferrochromium - Google Patents
Process for the production of low sulfur ferrochromium Download PDFInfo
- Publication number
- US3271139A US3271139A US186310A US18631062A US3271139A US 3271139 A US3271139 A US 3271139A US 186310 A US186310 A US 186310A US 18631062 A US18631062 A US 18631062A US 3271139 A US3271139 A US 3271139A
- Authority
- US
- United States
- Prior art keywords
- percent
- alloy
- ferrochromium
- slag
- carbon
- 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
- 238000000034 method Methods 0.000 title claims description 24
- 229910000604 Ferrochrome Inorganic materials 0.000 title claims description 22
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title claims description 21
- 229910052717 sulfur Inorganic materials 0.000 title claims description 21
- 239000011593 sulfur Substances 0.000 title claims description 21
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000000203 mixture Substances 0.000 claims description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 12
- 238000003723 Smelting Methods 0.000 claims description 10
- 229910000676 Si alloy Inorganic materials 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 description 29
- 239000000956 alloy Substances 0.000 description 29
- 239000011651 chromium Substances 0.000 description 20
- 229910052710 silicon Inorganic materials 0.000 description 20
- 239000010703 silicon Substances 0.000 description 20
- 239000002893 slag Substances 0.000 description 20
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 19
- 229910052751 metal Inorganic materials 0.000 description 17
- 239000002184 metal Substances 0.000 description 17
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 14
- 229910052804 chromium Inorganic materials 0.000 description 12
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 6
- 235000011941 Tilia x europaea Nutrition 0.000 description 6
- 239000012535 impurity Substances 0.000 description 6
- 239000004571 lime Substances 0.000 description 6
- 238000011084 recovery Methods 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000000470 constituent Substances 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000003245 coal Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229910001021 Ferroalloy Inorganic materials 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229910001339 C alloy Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/003—Making ferrous alloys making amorphous alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21B—MANUFACTURE OF IRON OR STEEL
- C21B11/00—Making pig-iron other than in blast furnaces
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/02—Making non-ferrous alloys by melting
Definitions
- the present invention relates to a process for producing ferrochromium alloys. More particularly, the present invention relates to a process for producing ferrochromium alloys having very low sulfur contents.
- Certain elements are known to cause highly undesirable effects when present as constituents in structural metals.
- sulfur is one of the most detrimental due to its adverse effects on the high-temperature properties of the metal.
- a process in accordance with the present invention for producing low sulfur ferrochromium comprises preparing ferrochromium metal substantially in the form of together with a fluid slag by smelting a mixture of chrome ore, carbon and slag-forming material in which mixture the molar base to acid ratio of the slag-forming material is between about 2.5 :1 and about 8.5 :1, preferably between 35 :1 and 6: 1, and in which the molar ratio of lime to silica is greater than about 0.75.
- Ferrochromium alloy which is produced from the usual source materials in accordance with the present invention has a sulfur content of less than about 0.015 percent, a silicon content of less than about 2 percent, and a phosphorous content of less than about 0.02 percent. As a consequence, this material is of high industrial utility.
- compositional ranges in weight percent of [ferrochromium alloys which can be readily produced in accordance with the present invention from the usual commercial starting materials are set forth in Table I.
- the oxygen-containing calcium and magnesium materials in the smelting mixture are considered to be in the form of CaO and MgO, respectively, and the aforementioned molar base to acid ratio of the slag forming material is calculated as follows:
- Alumina and other oxides present in the smelting mixture are not included in the computation of the base to acid ratio.
- a mixture of chrome ore, carbon, and slag-forming material is smelted in an electric furnace to provide molten ferro-chromium metal substantially in the form of (Fe,Cr)-;C together with a fluid, highly basic slag from which the metal is ultimately separated and solidified.
- chrome ores can be used in the present process and the carbon material in the furnace charge can be in any convenient form such as coal, coke, and the like.
- the charge can contain the usual amount of sulfur impurities which is generally between about 0.1 and 0.3 percent by weight. Substantially greater amounts of sulfur can be present in the charge and the alloy produced by the present invention will nevertheless have a surprisingly low sulfur content.
- the chrome ore can be in the form of lumps or fines and the tfines can be briquetted or not as desired. If fines are used and formed into briquets together with reductant and slag-forming material, a considerable saving in power consumption is realized.
- base to acid ratio of the slag-forming material be in the range of 2.5 :1 and 8.5 :1, preferably between 3.5 :1 and 6: 1, in order to ultimately provide a ferrochromium alloy with less than 0.015 percent sulfur. It is also necessary that the molar ratio of lime to silica in the charge be greater than about 0.75 to ensure a silicon content of less than 2 percent and to avoid an increase in sulfur content to above 0.015 percent. If the lime to silica ratio is less than about 0.75, silica becomes available for reduction which results in an increase in the silicon level of the alloy. At the same time, under these circumstances, the carbon content of the alloy decreases and the sulfur content increases.
- a further requirement of the present invention is that the slag produced in the smelting of the furnace charge be high melting and highly fluid in the molten state in order to be effective in the process and to permit convenient separation of the metal product.
- slags having a 25 poise temperature of at least 1575 C. are required in the present process.
- alumina can be added to the furnace charge in the amount required. This alumina addition, of course, does not affect the base to acid ratio of the charge.
- compositional ranges set forth in Table II are specific proportions of slag-forming materials which satisfy the present invention.
- Table III sets forth ranges for slag-forming material which can be used in the present invention providing the aforedescribed molar ratios are satisfied. In the tables and elsewhere in this description, only 0110, MgO,
- A1 and SiO; are considered as constituents of slagforming material; chrome and iron oxides and contaminants derived from the ore and reduetant are disregarded.
- the carbon stoichiometry is of importance and must be adjusted so that the final ferrochromium alloy is substantially, i.e. 95 percent or more, in the form of (Fe,Cr) C Accordingly, the preferred carbon content of the molten alloy prepared by smelting the furnace charge is 8 to 9 percent, although carbon contents up to 10 percent provide highly satisfactory ferrochromium alloys having sulfur contents below 0.015 percent and silicon contents below 2.0 percent.
- Carbon contents in the molten alloy which are higher than 10 percent are undesirable since they tend to cause the formation of substantial amounts of the Cr C type of carbide which is highly refractory and interferes with recovery of the alloy. Moreover, the amount of carbon required in the furnace charge to produce the higher carbon levels tends to cause an increase of silicon in the alloy.
- the silicon content of the ferroehromium alloy product of this invention is limited to less than about 2 percent by adjusting the lime to silica ratio in the furnace charge to 0.75 or more. Additionally, the silicon content of the alloy can be adjusted to particular values less than about 2.0 percent by controlling the carbon stoiehiometry and/or the sizing of the furnace charge constituents. For example, carbon in the charge, in excess of the stoiehiometric amount required to form (Fe,Cr)-;C by reduction of the ore, tends to cause an increase in the silicon content of the alloy. Also, decreasing the particle size of the furnace charge tends to increase the silicon content.
- the silicon content of the alloy can be controlled in the range from about 0.1 to about 2.0 percent.
- Control of the silicon content of the ferrochromium alloy is important in that silicon affects the solidity and the friability of the metal.
- Very low-silicon metal can be made by the present process, however if the silicon content is less than about 0.15 percent, the metal is gassy and full of small voids. A silicon content in the range of 0.5 to 2.0 percent will result in a dense, solid but still friable alloy. If the metal is to be used as an addition agent to a steel bath, it will be generally preferable to maintain the silicon content in the 0.5 to 2.0 percent range.
- the metal is to be further processed as by a solid state decarburizing process, the solidity and denseness of the metal are unimportant, and the silicon may be less than 0.5 percent if desired.
- a low-silicon content is advantageous when the molten metal is to be decarburized by oxygen blowing since this reduces slag formation resulting from oxidation of silicon and therefore refractory attack.
- the mix had a molar base to acid ratio of 5.93 and was calculated to produce the following products:
- the calculated slag composition is not adjusted for subsequently dissolved Cr O or volatilization and dusting losses.
- the mix was fed to an electric furnace having an oval hearth in which power was supplied by two 17-inch diameter electrodes.
- the furnace lining was rammed carbon paste with chrome ore refractory backup.
- the furnace was operated at about 1000 kilowatts at 60 to volts.
- the average composition of metal tapped from the furnace was as follows:
- the metal was gassy, i.e. contained numerous voids but was free of gross slag inclusions.
- Example 11 The following ⁇ mix was prepared as a furnace charge.
- This mix had a molar base to acid ratio of 6.92 and was calculated to produce the following products:
- the mix constituents were thoroughly mixed at a temperature sufficient to fluidize the binder and pressed into pillow-shaped briquets approximately 2% by 2 inches.
- the average composition of the metal produced was:
- the metal was solid and free of voids.
- Example III The following mix was prepared as a furnace charge.
- the mix was fed to the furnace described in Example I using an average power input of about 1000 kilowatts at 50 to 60 volts.
- the average composition of the metal and slag produced is as follows:
- the slags derived from the practice of the present invention generally contain less than 4 percent Cr O and frequently contain less than 1 percent Cr O Since the slags of conventional smelting processes usually contain from 5 to 8 percent Cr O it can be seen that the present invention provides a substantial increase in chromium recovery.
- the slag to alloy ratios obtained in the practice of the present invention range from 0.8 to 1.0 (fine ore practice) to 1.5 (lump ore practice) with the average being about 1.1 to 1.25. These ratios indicate a considerably higher metal recovery in the practice of the present invention than that obtained in previously known processes.
- the improvement for producing a low sulfur, low silicon alloy which comprises adjusting the composition of the mixture so that (1) the base to acid molar ratio of the mixture is between about 2.5:1 and 8.5: 1, (2) the CaO to SiO ratio of the mixture is greater than about 0.75, (3) the result- 8 ing slag has a 25 poise temperature of at least about 1575 C., and (4) the alloy produced is at least 95 percent in the form of (Fe,Cr)-;C
- a process in accordance with claim 1 wherein the slag forming material in the mixture is within the compositional range of 13 to percent CaO, 22 to 35 percent MgO, 25 to 42 percent A1 0 9 to 28 percent SiO 3.
- a process in accordance with claim 1 wherein the molar base to acid ratio is between 3.5 :1 and 6:1.
- a process for producing ferrochromium alloy by smelting a charge consisting essentially of chrome ore, carbon and at least one slag-forming material selected from the group consisting of CaO, SiO MgO and A1 0 to cause reduction of the ore and the production of ferrochromium and a basic slag the improvement for producing a low sulfur, low silicon high carbon alloy which comprises adjusting said charge to provide a base to acid molar ratio therein of between about 2.5:1 and 8.521 and a CaO to SiO ratio therein of greater than about 0.75 and to provide upon reduction of the chrome ore in said charge 1) a slag having a 25 poise temperature of at least 1575 C. and (2) a ferrochromium alloy which is at least 95% in the form of (Fe,Cr) C said alloy being characterized by having a sulfur content of less than 0.015 percent and a silicon content of less than 2. percent.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US186310A US3271139A (en) | 1962-04-10 | 1962-04-10 | Process for the production of low sulfur ferrochromium |
| GB11663/63A GB996221A (en) | 1962-04-10 | 1963-03-25 | Improvements in and relating to alloys |
| JP38017539A JPS5019486B1 (show.php) | 1962-04-10 | 1963-04-09 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US186310A US3271139A (en) | 1962-04-10 | 1962-04-10 | Process for the production of low sulfur ferrochromium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3271139A true US3271139A (en) | 1966-09-06 |
Family
ID=22684436
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US186310A Expired - Lifetime US3271139A (en) | 1962-04-10 | 1962-04-10 | Process for the production of low sulfur ferrochromium |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US3271139A (show.php) |
| JP (1) | JPS5019486B1 (show.php) |
| GB (1) | GB996221A (show.php) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5259866A (en) * | 1990-10-23 | 1993-11-09 | Japan Metals & Chemicals Co., Ltd. | Method for producing high-purity metallic chromium |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2206139A (en) * | 1938-07-23 | 1940-07-02 | Marvin J Udy | Chromium reduction |
| US2227287A (en) * | 1937-09-24 | 1940-12-31 | Marvin J Udy | Chromium metallurgy |
| US2238078A (en) * | 1939-01-23 | 1941-04-15 | Percy H Royster | Production of ferrochromium |
| US2280452A (en) * | 1941-04-10 | 1942-04-21 | Percy H Royster | Preparation of ferro-chromium in blast furnaces |
| US2286577A (en) * | 1939-03-09 | 1942-06-16 | Percy H Royster | Pyrometallurgical process for the production of pig-iron and ferrochromium |
| US2292495A (en) * | 1940-08-15 | 1942-08-11 | Marvin J Udy | Chromium recovery |
| US2332415A (en) * | 1940-08-15 | 1943-10-19 | Marvin J Udy | Chromium recovery |
-
1962
- 1962-04-10 US US186310A patent/US3271139A/en not_active Expired - Lifetime
-
1963
- 1963-03-25 GB GB11663/63A patent/GB996221A/en not_active Expired
- 1963-04-09 JP JP38017539A patent/JPS5019486B1/ja active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2227287A (en) * | 1937-09-24 | 1940-12-31 | Marvin J Udy | Chromium metallurgy |
| US2206139A (en) * | 1938-07-23 | 1940-07-02 | Marvin J Udy | Chromium reduction |
| US2238078A (en) * | 1939-01-23 | 1941-04-15 | Percy H Royster | Production of ferrochromium |
| US2286577A (en) * | 1939-03-09 | 1942-06-16 | Percy H Royster | Pyrometallurgical process for the production of pig-iron and ferrochromium |
| US2292495A (en) * | 1940-08-15 | 1942-08-11 | Marvin J Udy | Chromium recovery |
| US2332415A (en) * | 1940-08-15 | 1943-10-19 | Marvin J Udy | Chromium recovery |
| US2280452A (en) * | 1941-04-10 | 1942-04-21 | Percy H Royster | Preparation of ferro-chromium in blast furnaces |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5259866A (en) * | 1990-10-23 | 1993-11-09 | Japan Metals & Chemicals Co., Ltd. | Method for producing high-purity metallic chromium |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5019486B1 (show.php) | 1975-07-08 |
| GB996221A (en) | 1965-06-23 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: ELKEM METALS COMPANY, 270 PARK AVE., NEW YORK, NY Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:UNION CARBIDE CORPORATION;REEL/FRAME:003882/0752 Effective date: 19810626 Owner name: ELKEM METALS COMPANY, 270 PARK AVENUE, NEW YORK, N Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:UNION CARBIDE CORPORATION, A NY CORP.;REEL/FRAME:003882/0761 Effective date: 19810626 Owner name: ELKEM METALS COMPANY, A GENERAL PARTNERSHIP OF NY, Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:UNION CARBIDE CORPORATION;REEL/FRAME:003882/0752 Effective date: 19810626 Owner name: ELKEM METALS COMPANY, A NEW YORK GENERAL PARTNERSH Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:UNION CARBIDE CORPORATION, A NY CORP.;REEL/FRAME:003882/0761 Effective date: 19810626 |