US3836613A - Method of making liner in an induction melting furnace - Google Patents
Method of making liner in an induction melting furnace Download PDFInfo
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- US3836613A US3836613A US00194949A US19494971A US3836613A US 3836613 A US3836613 A US 3836613A US 00194949 A US00194949 A US 00194949A US 19494971 A US19494971 A US 19494971A US 3836613 A US3836613 A US 3836613A
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- liner
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- 230000006698 induction Effects 0.000 title abstract description 16
- 238000002844 melting Methods 0.000 title abstract description 11
- 230000008018 melting Effects 0.000 title abstract description 11
- 238000004519 manufacturing process Methods 0.000 title 1
- 239000000203 mixture Substances 0.000 abstract description 56
- 238000000034 method Methods 0.000 abstract description 15
- 239000011044 quartzite Substances 0.000 abstract description 13
- 239000011230 binding agent Substances 0.000 description 27
- 238000005245 sintering Methods 0.000 description 14
- 239000002694 phosphate binding agent Substances 0.000 description 11
- 239000003795 chemical substances by application Substances 0.000 description 10
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 239000011819 refractory material Substances 0.000 description 5
- 239000002344 surface layer Substances 0.000 description 5
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 4
- 239000004327 boric acid Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 238000005728 strengthening Methods 0.000 description 4
- 238000005056 compaction Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920001353 Dextrin Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000004568 cement Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 238000012856 packing Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- -1 polyoxychloride Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical class O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000019351 sodium silicates Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000008646 thermal stress Effects 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 241001605719 Appias drusilla Species 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 229910001141 Ductile iron Inorganic materials 0.000 description 1
- 229910001060 Gray iron Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000007767 bonding agent Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000003870 refractory metal Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052566 spinel group Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/16—Making or repairing linings ; Increasing the durability of linings; Breaking away linings
- F27D1/1626—Making linings by compacting a refractory mass in the space defined by a backing mould or pattern and the furnace wall
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/14—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silica
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27B—FURNACES, KILNS, OVENS OR RETORTS IN GENERAL; OPEN SINTERING OR LIKE APPARATUS
- F27B14/00—Crucible or pot furnaces
- F27B14/06—Crucible or pot furnaces heated electrically, e.g. induction crucible furnaces with or without any other source of heat
- F27B14/061—Induction furnaces
Definitions
- a dry refractory tertiary quartzite granular composition is filled between the furnace wall and a form defining the inner shape of the liner and densified as by vibration applied to the form.
- the form is removed to leave a selfsupporting liner.
- the exposed inner surface of the liner is impregnated with a binder to a depth less than the total thickness of the liner to form an inner strengthened shell having a thickness of from 1-8 mm.
- the inner shell is then sintered leaving the outer zone of said linear unsintered.
- Induction melting furnace of the crucible and trough type are generally lined with plastic, semi-plastic and/or dry compositions having a base of a refractory metal oxide such as MgO, A1 0 SiO spinels, and the like.
- the refractory lining is rammed up with the refractory composition, also called fritting composition, with the aid of a precisely centered sheet-metal form which creates a cavity, or the composition is poured in and vibrated.
- the sintering agent which is usually in the form of boric acid, must be mixed in dry form with the composition.
- Such dry compositions are rammed up or vibrated in place with the aid of a form which in this case 3,836,613 Patented Sept. 17, 1974 serves both for the transfer of the energy, e.g., by vibration to densify the loose granular mixture, and, mainly, for the purpose of giving stability to the granular mixture.
- the object of the invention is to create a self-supporting liner which eliminates the losses involved in forms expended during construction of the liner, but provides the greatest possible protection against mechanical and thermal stresses.
- this invention contemplates a self-supporting liner for an induction melting furnace constructed of an unsintered densified mass of a refractroy oxide or mixture of oxides having on its inside surface intergral therewith a shell consisting of the same mass but containing a binding agent which becomes stronger at elevated temperatures.
- This invention further contemplates a method for preparing a self-supporting liner for an induction melting furnace which method comprises the steps of:
- a self-supoprting liner for an induction furnace is made, pursuant to the present invention, by filling a form within the furnace which form defines the space to be filled. Such space when filled constitutes the liner.
- the liner is filled with a dry refractory material, especially a refractory material of the tertiary quartzite type having a grain configuration of round to cubic.
- the refractory material is in admixture with a sintering agent, desirably dry boric acid.
- Vibrational energy is applied to the so-filled form. This energy effects compacting the loose granular mixture to a dense mass and provides stability to the granular mixture.
- binding agent which becomes stronger at elevated temperatures.
- binding agents include phosphate binding agents especially monoaluminum phosphate and derivatives thereof containing phosphorus.
- the binding agents effect is to impart durability and mechanical strength to the liner before and when being sintered. While the amount of binding agent can vary over a wide range, a quantity between 0.05 and 0.07 cubic centimeters of binding agent per square centimeter of surface area treated is enough. Generally spoken, the quantity of binder suffices which is sucked in by the dry liner material on the inside surface.
- the inside wall is subjected to a temperature between 400 and 700 C. to effect strengthening the inner shell of the wall and to provide the same with good mechanical properties.
- a self-supporting liner comprising, on the coil side exclusively, a highly compacted, dry granular structure of refractory oxide or oxide mixture to which a dry sintering agent, preferably boric acid, has been added is provided.
- the inner surface layer of said liner has an integral shell comprising a binding agent which becomes stronger at elevated temperatures which has been subjected to elevated temperatures.
- the thickness of the strengthened shell is preferably provided by applying to the inner surface layer a binding agent especially a phosphate binding agent, particularly a monoaluminum phosphate binder with variable phosphate members.
- a binding agent especially a phosphate binding agent, particularly a monoaluminum phosphate binder with variable phosphate members.
- suitable binders include, for example, sodium silicates of varying soda to silica ratio (such as water glass), silicic acid esters, tar, dextrine solutions, and sulfite waste liquor.
- the preferred starting material for these refractory compositions are quartzites having a tertiary quartzite base, since they have a round to cubic grain which is particularly well suited for dense packing. These quartzites are fine to coarsely crystalline in their mineralogical nature, and they may or may not contain a binding agent, for example, the so-called basal cement.
- FIG. 1 is a graph summarizing the eifect of temperature of expansion for three different compositions.
- FIG. 2 shows the grain size and configuration of re fractory metals used in the liner of the present invention.
- FIG. 3 is a cross-sectional diagram showing a liner, form and furnace during construction.
- FIG. 1 shows the expansion characteristics of the compositions as a percentage, in relation to the temperature in C.
- the three compositions show a like expansion up to about C., but above this temperature they differ, in that Composition B tends to shrink while Composition A and Composition C have an expansion of just under 9% at about 1600 C.
- the invention utilizes these expansion characteristics, and it is pointed out that in crucible furnaces the refractory liner is an annular body which in the case of expansion, due to the effect of temperature, for example, can only increase in diameter.
- the thermal expansion characteristics be adjusted on the basis of the mineralogy of the refractory liner, preferably tertiary quartzite, and on the basis of the amount of sintering agent used, in such a manner that in the 1600 C. temperature range, and with a sintering agent content of 1%, an expansion of the refrac tory composition of 7 to 9% will be achieved.
- Example A is best performed by a liner having a tertiary quartzite base material with round to cubic grain form.
- the grain form can be produced by appropriate precessing of the very hard rock.
- the tertiary quartzite with a basal cement structure, which is used here, is substantially harder than a rock quartzite.
- the least suitable grain form is also shown in FIG. 2, and is marked B. It is a grain form existing preferably in crushed rock quartzites, see curves B and C in FIG. 1.
- Another feature of the invention is the adjustment of the grain analysis in such a manner that, on the one hand, an optimum compaction is possible, and on the other hand, there is still room for further compaction in grain interstices when the annular furnace liner undergoes thermal expansion.
- Examples of the grain composition of the invention are given in Table 1 at the end of this description, by way of example. Accordingly, 60 to 40% of the grain composition consists of grains of 5.0 to 0.6 mm., 30% of grains smaller than 0.06 mm., and the balance of 0.6 and 0.06 mm. grains.
- energy is delivered through the inserted form which establishes the cavity in the refractory grain mixture, to a suflicient extent to produce an optimum density.
- This furnace lining is not, of course, sufiiciently stable to withstand mechanical stresses, such as, for example, those produced by the vibrations of the electrical energy of the induction coil-
- a phosphate binder is added to the self-supporting furnace liner after removal of the form.
- FIG. 3 is a cross section of the crucible of an induction furnace which consists of an outer wall 1, an intermediate form 2 and the refractory liner 3. The latter is adjoined on the inside by'the form 4, which is removed after the compaction or densification in order then to permit the application of the phosphate binder to the surface of the refractory liner 3, which is preferably performed by spraying.
- a special mineral-chemical binder is added to the portion of the liner adjacent the melt.
- This is a phosphate binder, preferably a monoaluminum phosphate binder with variable phosphate members.
- binders which may also contain chromium oxide additives, develop strengths between and 20 kg./ crn. even at room temperature when added in quantities of 6 to 8% to the dry granular mixture.
- a liner in accordance with the invention it is desirable to prepare a liner in accordance with the invention in such a manner that the dry, refractory granular composition, mixed with the dry sintering agent, is compacted in the furnace to a total pore volume of 16 to 24%, using a removable, re-usable form. The form is then removed and the inner layer of the liner is impregnated with the binding agent.
- the furnace can be started up in the customary manner using a burner system, a starting ingot and/or a batch of molten metal, because the liner creates conditions no difierent from those known in the past.
- the cavity between furnace wall and form was filled up with dry tertiary quartzite having a grain size composition as described in Example 1 of Table 1 in mixture with dry boric acid (1% of the mass).
- a vibrator driven by compressed air was attached to the form and put into operation for 6 minutes. Thereafter the form was re moved from the furnace.
- On the interior surface of the liner monoaluminum phosphate was sprayed in a quantity of 1 litre per square meter of the surface. Thereafter, the lining was heated to 400 C. by induction heating. Finally the furnace was charged with material to be melted and heated to melting temperatures above 1500 C. During this heating the inner shell of the liner was sintered, whereas the outer zones of the liner remained unsintered.
- Example 1 Example 2
- Example 3 Grain size composition (mm.) (percent) (p ereent) (percent) Total 43. 45 54. 60 57. 15
- heating step (e) is carried out at a temperature between 400 and 700 C.
- binding agent is selected from the group consisting of sodium silicates, silicic acid esters, tar, dextrine solutions and sulphite waste liquor.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Furnace Housings, Linings, Walls, And Ceilings (AREA)
- Compositions Of Oxide Ceramics (AREA)
Abstract
A METHOD OF PREPARING A SELF SUPPORTING LINER FOR AN INDUCTION MELTING FURANCE IS DISCLOSED. A DRY REFRACTORY TERTIARY QUARTZITE GRANULAR COMPOSITION IS FILLED BETWEEN THE FURNACE WALL AND A FORM DEFINING THE INNER SHAPE OF THE LINER AND DENSIFIED AS BY VIBRATION APPLIED TI THE FORM. THE FORM IS REMOVED TO LEAVE A SELFSUPPORTING LINER. THE EXPOSED INNER SURFACE OF THE LINER IS IMPREGNATED WITH A BINDER TO A DEPTH LESS THAN THE TOTAL THICKNESS OF THE LINER TO FORM AN INNER STRENGTHENED SHELL HAVING A THICKNESS OF FROM 1-8 MM. THE INNER SHELL IS THEN SINTERED LEAVING THE OUTER ZONE OF SAID LINEAR UNSINTERED.
Description
Sept. 17, 1974 K GRANITZKI ETAL 3,836,613
MASS A I Q MASS B------ g I MASS c-'--- O- I l l I I I I I I 500 I000 \I70O TEMPERATURE IN c I\ I\ I 4 I I I I I 'I I\ a I I l I I l l I I I I I I \I I I I l I l l I\ I l S apt. 11, 1014 K. E. GRAN iTZKl ETAL 3,836,613
A dry refractory tertiary quartzite granular composition is filled between the furnace wall and a form defining the inner shape of the liner and densified as by vibration applied to the form. The form is removed to leave a selfsupporting liner. The exposed inner surface of the liner is impregnated with a binder to a depth less than the total thickness of the liner to form an inner strengthened shell having a thickness of from 1-8 mm. The inner shell is then sintered leaving the outer zone of said linear unsintered.
BACKGROUND OF THE INVENTION Field of the invention Induction melting furnace of the crucible and trough type are generally lined with plastic, semi-plastic and/or dry compositions having a base of a refractory metal oxide such as MgO, A1 0 SiO spinels, and the like. The refractory lining is rammed up with the refractory composition, also called fritting composition, with the aid of a precisely centered sheet-metal form which creates a cavity, or the composition is poured in and vibrated. It is then necessary to frit the refractory composition, i.e., a heating and drying process must be performed on the furnace lining, which is a tedious procedure depending on the nature of the refractory material, so that the present time from 12 to 24 hours of preparation are required when a dry composition is used, and up to a week or more when plastic compositions are used. There is a genuine need to reduce the amount of time required for the lining of the furnace to make the melting unit ready for operation.
An improvement can be achieved by using absolutely dry granular mixtures as the refractory composition. In this case the sintering agent, which is usually in the form of boric acid, must be mixed in dry form with the composition. Such dry compositions are rammed up or vibrated in place with the aid of a form which in this case 3,836,613 Patented Sept. 17, 1974 serves both for the transfer of the energy, e.g., by vibration to densify the loose granular mixture, and, mainly, for the purpose of giving stability to the granular mixture.
In the known state of the art it is not possible to make a self-supporting refractory liner in an induction melting furnace from a loose composition without using a form until the sintering of the granular mixture is completed. This means that the form, which generally costs several times as much as the refractory composition, remains in the furnace, is heated up with a gas or oil flame or by electrical power to the point where the granular mixture containing the sintering agents solidifies ceramically. In this process the form is melted; otherwise, it eventually melts when the furnace is charged with molten material or a solid charge is melted down in it.
According to Giesserei 57 (1970), pp. 450-451, tests were recently started on a plastic quartzite composition with a binder consisting of several components (monoaluminum phosphate, inorganic polymeric binders having a polyoxychloride base and other components), with a re-usable form. A number of advantages are expected from this. However, the fact that the liner solidifies into an integral pot from the inside surface all the way to the outside surface does not prevent the danger of cracks running all the way through enabling the melt to penetrate through to the water-cooled coil.
The object of the invention is to create a self-supporting liner which eliminates the losses involved in forms expended during construction of the liner, but provides the greatest possible protection against mechanical and thermal stresses.
SUMMARY OF THE INVENTION Broadly, this invention contemplates a self-supporting liner for an induction melting furnace constructed of an unsintered densified mass of a refractroy oxide or mixture of oxides having on its inside surface intergral therewith a shell consisting of the same mass but containing a binding agent which becomes stronger at elevated temperatures.
This invention further contemplates a method for preparing a self-supporting liner for an induction melting furnace which method comprises the steps of:
A. Filling the space between a form defining the shape of the liner to be constructed and the furnace wall with a dry refractory granular composition and a dry sintering agent and densifying the liner mass B. Removing said form- C. Applying to the inside wall of the liner a binding agent which becomes stronger at elevated temperature D. Heating the so-treated liner to effect formation of an integral shell on the inside surface of said self-supporting liner before or during sintering said internal shell.
Generally speaking, a self-supoprting liner for an induction furnace is made, pursuant to the present invention, by filling a form within the furnace which form defines the space to be filled. Such space when filled constitutes the liner. The liner is filled with a dry refractory material, especially a refractory material of the tertiary quartzite type having a grain configuration of round to cubic. The refractory material is in admixture with a sintering agent, desirably dry boric acid.
3 Vibrational energy is applied to the so-filled form. This energy effects compacting the loose granular mixture to a dense mass and provides stability to the granular mixture.
After the vibrational energy is applied, the form is Withdrawn to expose the inside wall of the liner. To the inner surface of the liner is applied a binding agent which becomes stronger at elevated temperatures. Particularly suitable binding agents include phosphate binding agents especially monoaluminum phosphate and derivatives thereof containing phosphorus. The binding agents effect is to impart durability and mechanical strength to the liner before and when being sintered. While the amount of binding agent can vary over a wide range, a quantity between 0.05 and 0.07 cubic centimeters of binding agent per square centimeter of surface area treated is enough. Generally spoken, the quantity of binder suffices which is sucked in by the dry liner material on the inside surface.
After the binding agent is applied to the inside wall of the liner, the inside wall is subjected to a temperature between 400 and 700 C. to effect strengthening the inner shell of the wall and to provide the same with good mechanical properties.
DESCRIPTION OF PREFERRED EMBODIMENTS In accordance with the invention, a self-supporting liner comprising, on the coil side exclusively, a highly compacted, dry granular structure of refractory oxide or oxide mixture to which a dry sintering agent, preferably boric acid, has been added is provided. The inner surface layer of said liner has an integral shell comprising a binding agent which becomes stronger at elevated temperatures which has been subjected to elevated temperatures.
It is desirable for the thickness of the strengthened shell to amount to between 1 and 8 mm. This strengthening shell is preferably provided by applying to the inner surface layer a binding agent especially a phosphate binding agent, particularly a monoaluminum phosphate binder with variable phosphate members. Other suitable binders include, for example, sodium silicates of varying soda to silica ratio (such as water glass), silicic acid esters, tar, dextrine solutions, and sulfite waste liquor.
Preference is given to an acidic lining, since induction furnaces for the melting of non-ferrous metals and gray iron, ductile iron and cast steel are today mostly (more than 90%) lined with refractory compositions of an acidic substance. In accordance with the invention, the preferred starting material for these refractory compositions are quartzites having a tertiary quartzite base, since they have a round to cubic grain which is particularly well suited for dense packing. These quartzites are fine to coarsely crystalline in their mineralogical nature, and they may or may not contain a binding agent, for example, the so-called basal cement. Depending on the temperature and the transformation tendency, thermal stresses are present for the formation of the individual modifications which exists, ranging from more than down to shrinking tendencies in the temperature range up to 1600 C. Shrinkage is determined also by the sintering agent in the case of certain types of quartzites. Conventional fritting compositions can be employed.
BRIEF DESCRIPTION OF DRAWINGS FIG. 1 is a graph summarizing the eifect of temperature of expansion for three different compositions. I
FIG. 2 shows the grain size and configuration of re fractory metals used in the liner of the present invention.
FIG. 3 is a cross-sectional diagram showing a liner, form and furnace during construction.
In FIG. 1 this situation is summarized by the example of three compositions, A, B and C. FIG. 1 shows the expansion characteristics of the compositions as a percentage, in relation to the temperature in C. The three compositions show a like expansion up to about C., but above this temperature they differ, in that Composition B tends to shrink while Composition A and Composition C have an expansion of just under 9% at about 1600 C. The invention utilizes these expansion characteristics, and it is pointed out that in crucible furnaces the refractory liner is an annular body which in the case of expansion, due to the effect of temperature, for example, can only increase in diameter. This is advantageous for the liner, because if the grain size analysis is correct, the loose granular mixture will thus be further compressed to such an extent that its porosity can be reduced to values in the neighborhood of 10% If, however, a composition behaves like the one in Example B, the result will be cracks in the refractory lining, due to the fact that the composition shrinks owing, for example, to the influence of the sintering agent. These cracks impair the life of the liner and lead to an early failure of the furnace. According to the invention, therefore, it is proposed that the thermal expansion characteristics be adjusted on the basis of the mineralogy of the refractory liner, preferably tertiary quartzite, and on the basis of the amount of sintering agent used, in such a manner that in the 1600 C. temperature range, and with a sintering agent content of 1%, an expansion of the refrac tory composition of 7 to 9% will be achieved.
In addition to the mineralogy of the raw material, which greatly affects the transformation and expansion characteristics of the refractory composition, the shape of the grains and the grain analysis are of great importance for the achievement of an optimum packing density towards the solution of the problem to which the invention is addressed. Example A is best performed by a liner having a tertiary quartzite base material with round to cubic grain form. The grain form can be produced by appropriate precessing of the very hard rock. The tertiary quartzite with a basal cement structure, which is used here, is substantially harder than a rock quartzite. The least suitable grain form is also shown in FIG. 2, and is marked B. It is a grain form existing preferably in crushed rock quartzites, see curves B and C in FIG. 1.
Another feature of the invention is the adjustment of the grain analysis in such a manner that, on the one hand, an optimum compaction is possible, and on the other hand, there is still room for further compaction in grain interstices when the annular furnace liner undergoes thermal expansion. Examples of the grain composition of the invention are given in Table 1 at the end of this description, by way of example. Accordingly, 60 to 40% of the grain composition consists of grains of 5.0 to 0.6 mm., 30% of grains smaller than 0.06 mm., and the balance of 0.6 and 0.06 mm. grains. By means of a suitable vibrator system, energy is delivered through the inserted form which establishes the cavity in the refractory grain mixture, to a suflicient extent to produce an optimum density.
In Table 2 below the crude densities are given which were determined in a three-ton furnace and which were found on the basis of test body sleeves vibrated into' the furnace liner. At the net density peculiar to thistype of quartzite, of 2.63 g./cm. total porosities of 16 to 20% were achieved. Texture data are thus available which represent optimums even in the case of formed and fired refractory bricks. In a number of series of experiments it was determined that a granular mixture compacted in this manner is sufficiently stable even without additional strengthening means to be self-supporting after removal of the form. This furnace lining is not, of course, sufiiciently stable to withstand mechanical stresses, such as, for example, those produced by the vibrations of the electrical energy of the induction coil- In a subsequent step in accordance with the invention, therefore, a phosphate binder is added to the self-supporting furnace liner after removal of the form.
The laminated liner prepared in this manner can be seen in FIG. 3. FIG. 3 is a cross section of the crucible of an induction furnace which consists of an outer wall 1, an intermediate form 2 and the refractory liner 3. The latter is adjoined on the inside by'the form 4, which is removed after the compaction or densification in order then to permit the application of the phosphate binder to the surface of the refractory liner 3, which is preferably performed by spraying. In the laminated liner of the invention, a special mineral-chemical binder is added to the portion of the liner adjacent the melt. This is a phosphate binder, preferably a monoaluminum phosphate binder with variable phosphate members. The following compositions, for example, are thus possible:
1. Monaluminum phosphate P 33.20%, free P 0 2.06%, A1 0 7.50%, free Al 0%, Al (H PO 46.50% 2. Acid phosphate binder with 40-45% by weight solid content, residue after firing consisting of P 0 A1 0 CI'2O3 3. Phosphate binder having condensed alkaline phosphates with a linear chain.
These binders, which may also contain chromium oxide additives, develop strengths between and 20 kg./ crn. even at room temperature when added in quantities of 6 to 8% to the dry granular mixture.
It is desirable to prepare a liner in accordance with the invention in such a manner that the dry, refractory granular composition, mixed with the dry sintering agent, is compacted in the furnace to a total pore volume of 16 to 24%, using a removable, re-usable form. The form is then removed and the inner layer of the liner is impregnated with the binding agent.
It is advantageous to spray the phosphate binder onto the inside surface of the liner, a sufiicient quantity being 0.05 to 0.07 cm. of binding agent absorbed by each square centimeter of surface area in the predetermined depth. This small amount of binding agent makes possible a very rapid and elfective drying, an advantage being that the slight amount of moisture can easily escape into the open furnace area.
It is also desirable to heat up the furnace chamber by means of a fuel burner such that the refractory composition in the shell attains a temperature of 400 to 700 C. When the liner has this temperature the crystallization water is driven out of the binding agent and its crystal structure is destroyed, so that if it is necessary to let the liner stand exposed to the air so that it cools, hygroscopicity is no longer present.
The furnace can be started up in the customary manner using a burner system, a starting ingot and/or a batch of molten metal, because the liner creates conditions no difierent from those known in the past.
EXAMPLE A middle frequency induction crucible furnace having a capacity of 1.5 tons was given a liner of 80mm. thickness. A divided reusable form having an outer diameter of 70 cm. was put into the furnace.
The cavity between furnace wall and form Was filled up with dry tertiary quartzite having a grain size composition as described in Example 1 of Table 1 in mixture with dry boric acid (1% of the mass). A vibrator driven by compressed air was attached to the form and put into operation for 6 minutes. Thereafter the form was re moved from the furnace. On the interior surface of the liner monoaluminum phosphate was sprayed in a quantity of 1 litre per square meter of the surface. Thereafter, the lining was heated to 400 C. by induction heating. Finally the furnace was charged with material to be melted and heated to melting temperatures above 1500 C. During this heating the inner shell of the liner was sintered, whereas the outer zones of the liner remained unsintered.
TABLE 1 Example 1 Example 2 Example 3 Grain size composition (mm.) (percent) (p ereent) (percent) Total 43. 45 54. 60 57. 15
0. .6 7. 95 5. 95 4. 65 0.23.3 3. 70 2. 20 1. 40 0.1-0.2 10. 60 4. 75 6. 00 0.060.1 5. 35 2. 3. 50 Below 0.06 28. 95 29. 70 27. 30
Total 56. 55 45. 40 42.
TABLE 2 Density in grams Test Number: per cubic centimeter 1 2.10
We claim: 1. Method for preparing a self-supporting hner for an induction melting furnace which comprises:
(a) preparing a mixture of a dry refractory granular quartzite composition having a tertiary quartzite base, said composition consisting of 40% to 60% of grains having a size between 0.6 and 5.0 mm., up to 30% of grains having a size of less than 0.06 mm. and balance grains having a size between 0.6 and 0.06 mm., said grains being round to cubic in configuration;
(b) filling the space between the furnace wall and a form defining the inner shape of the liner to be formed with the mixture prepared in (a);
(c) applying vibrational energy to densify the mixture in said space to a dense mass having a total pore volume of 16 to 24%;
(d) removing said form leaving a self-supporting liner;
(e) impregnating the exposed inner surface layer of said self-supporting liner with a binding agent to a predetermined depth less than the total thickness of the self-supporting liner thereby imparting durability and mechanical strength to said liner prior 0t and during sintering of said impregnated surface layer;
(f) heating said liner to form an inner strengthening shell having a thickness between 1 and 8 mm.; and thereafter (g) sintering the inner shell of said liner, the zone of said liner between said inner shell and said furnace wall remaining unsintered.
2. Method of claim 1 wherein the inner surface layer of said liner is sprayed with said binding agent in an amount such that between about 0.05 and 0.07 cubic centimeters of said binding agent are absorbed by each square centimeter of surface area in said predetermined depth.
3. Method of claim 1 wherein heating step (e) is carried out at a temperature between 400 and 700 C.
4. Method of claim 1 wherein said binding agent is a phosphate binding agent.
5. Method of claim 4 wherein said phosphate bonding agent is a monoaluminum phosphate.
6. Method of claim 1 wherein said binding agent is selected from the group consisting of sodium silicates, silicic acid esters, tar, dextrine solutions and sulphite waste liquor.
7. Method of claim 1 wherein the space between the furnace Wall and said form is annular.
References Cited UNITED STATES PATENTS Veale 264-62 Knapp 264-62 10 Rydinger et a1 1330 Renkey et a1. 266-43 Nordlie' .l 26430 Ash 264-30 Heimgartner 264-30 Felice et a1 2-64-30 Owen et a1 26430 ROBERT F. WHITE, Primary Examiner T. P. PAVELKO, Assistant Examiner U.S. c1. X.R.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2054136A DE2054136C2 (en) | 1970-11-04 | 1970-11-04 | Self-standing chuck in an induction melting furnace and method for its manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3836613A true US3836613A (en) | 1974-09-17 |
Family
ID=5787090
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00194949A Expired - Lifetime US3836613A (en) | 1970-11-04 | 1971-11-02 | Method of making liner in an induction melting furnace |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3836613A (en) |
| DE (1) | DE2054136C2 (en) |
| FR (1) | FR2112459B1 (en) |
| GB (1) | GB1372534A (en) |
| IT (1) | IT943640B (en) |
| SE (1) | SE376651B (en) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4218418A (en) * | 1978-06-22 | 1980-08-19 | Crystal Systems, Inc. | Processes of casting an ingot and making a silica container |
| WO1982003451A1 (en) * | 1981-03-31 | 1982-10-14 | Zhukov Leonid Fedorovich | Method of lining a metallurgical plant |
| US4818224A (en) * | 1987-12-11 | 1989-04-04 | Shell Oil Company | Process |
| US5495495A (en) * | 1995-05-25 | 1996-02-27 | Saint-Gobain/Norton Industrial Ceramics Corporation | Dense lining for coreless induction furnace |
| US10295260B2 (en) | 2016-10-18 | 2019-05-21 | Saint-Gobain Ceramics & Plastics, Inc. | Ceramic liner and method of forming |
| CN114383390A (en) * | 2021-12-30 | 2022-04-22 | 潍坊信合节能科技有限公司 | Medium-frequency induction diathermy furnace and medium-frequency induction diathermy furnace lining drying process |
| US20230349638A1 (en) * | 2022-04-05 | 2023-11-02 | Doggone Investment Co. LLC | Apparatus and method for production of high purity copper-based alloys |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2612912C2 (en) * | 1976-03-26 | 1984-09-06 | Dörentruper Sand- und Thonwerke GmbH, 4926 Dörentrup | Method and device for completing a melting furnace |
| BE837268A (en) * | 1975-12-31 | 1976-06-30 | IMPROVED REFRACTORY MATERIALS INTENDED TO CONSTITUTE THE INTERIOR COATING OF OVENS FOR METALLURGIC USE AND MORE SPECIFICALLY OF ELECTRIC INDUCTION OVENS | |
| DE3725173A1 (en) * | 1987-07-29 | 1989-02-16 | Fleischmann Adolf A Fa | Hot-repair method on channel induction furnaces for molten metals |
| GB2393500B (en) * | 2003-01-29 | 2004-09-08 | Morgan Crucible Co | Induction furnaces and components |
| CN102584187B (en) * | 2012-01-16 | 2013-10-16 | 芜湖市天地电子科技有限公司 | High-boron tube and preparation method thereof |
-
1970
- 1970-11-04 DE DE2054136A patent/DE2054136C2/en not_active Expired
-
1971
- 1971-10-26 SE SE7113564A patent/SE376651B/xx unknown
- 1971-10-29 IT IT30532/71A patent/IT943640B/en active
- 1971-11-02 US US00194949A patent/US3836613A/en not_active Expired - Lifetime
- 1971-11-03 GB GB5106571A patent/GB1372534A/en not_active Expired
- 1971-11-04 FR FR7139586A patent/FR2112459B1/fr not_active Expired
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4218418A (en) * | 1978-06-22 | 1980-08-19 | Crystal Systems, Inc. | Processes of casting an ingot and making a silica container |
| WO1982003451A1 (en) * | 1981-03-31 | 1982-10-14 | Zhukov Leonid Fedorovich | Method of lining a metallurgical plant |
| US4480820A (en) * | 1981-03-31 | 1984-11-06 | Institut Problem Litia Akademii Nauk Ukrainskoi Ssr | Method of lining metallurgical assembly |
| US4818224A (en) * | 1987-12-11 | 1989-04-04 | Shell Oil Company | Process |
| US5495495A (en) * | 1995-05-25 | 1996-02-27 | Saint-Gobain/Norton Industrial Ceramics Corporation | Dense lining for coreless induction furnace |
| DE19621423A1 (en) * | 1995-05-25 | 1996-12-12 | Saint Gobain Norton Ind Cerami | Coreless induction furnace and process for its manufacture |
| US10295260B2 (en) | 2016-10-18 | 2019-05-21 | Saint-Gobain Ceramics & Plastics, Inc. | Ceramic liner and method of forming |
| US11181321B2 (en) | 2016-10-18 | 2021-11-23 | Saint-Gobain Ceramics & Plastics, Inc. | Ceramic liner and method of forming |
| CN114383390A (en) * | 2021-12-30 | 2022-04-22 | 潍坊信合节能科技有限公司 | Medium-frequency induction diathermy furnace and medium-frequency induction diathermy furnace lining drying process |
| US20230349638A1 (en) * | 2022-04-05 | 2023-11-02 | Doggone Investment Co. LLC | Apparatus and method for production of high purity copper-based alloys |
| US11993828B2 (en) * | 2022-04-05 | 2024-05-28 | Doggone Investment Co. LLC | Apparatus and method for production of high purity copper-based alloys |
| US12234531B2 (en) | 2022-04-05 | 2025-02-25 | Doggone Investment Co. LLC | Apparatus and method for production of high purity copper-based alloys |
| US12371760B2 (en) | 2022-04-05 | 2025-07-29 | Doggone Investment Co. LLC | Apparatus and method for production of high purity copper-based alloys |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2054136A1 (en) | 1972-05-25 |
| GB1372534A (en) | 1974-10-30 |
| FR2112459A1 (en) | 1972-06-16 |
| IT943640B (en) | 1973-04-10 |
| FR2112459B1 (en) | 1977-01-28 |
| DE2054136C2 (en) | 1975-04-10 |
| SE376651B (en) | 1975-06-02 |
| DE2054136B2 (en) | 1972-05-25 |
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