CA2332797A1 - Conglomeration of minerals from a granular state with binder including waterglass, acrylic resin and vinyl alcohol - Google Patents
Conglomeration of minerals from a granular state with binder including waterglass, acrylic resin and vinyl alcohol Download PDFInfo
- Publication number
- CA2332797A1 CA2332797A1 CA002332797A CA2332797A CA2332797A1 CA 2332797 A1 CA2332797 A1 CA 2332797A1 CA 002332797 A CA002332797 A CA 002332797A CA 2332797 A CA2332797 A CA 2332797A CA 2332797 A1 CA2332797 A1 CA 2332797A1
- Authority
- CA
- Canada
- Prior art keywords
- binder
- mineral
- conglomeration
- acrylic resin
- vinyl alcohol
- 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.)
- Abandoned
Links
- 239000011230 binding agent Substances 0.000 title claims abstract description 41
- 229910052500 inorganic mineral Inorganic materials 0.000 title claims abstract description 37
- 239000011707 mineral Substances 0.000 title claims abstract description 37
- 229920000178 Acrylic resin Polymers 0.000 title claims abstract description 11
- 239000004925 Acrylic resin Substances 0.000 title claims abstract description 11
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 title claims abstract description 11
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 235000019353 potassium silicate Nutrition 0.000 title description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims abstract description 16
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 9
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 9
- 238000003723 Smelting Methods 0.000 claims abstract description 8
- 229910021538 borax Inorganic materials 0.000 claims abstract description 8
- 229910001629 magnesium chloride Inorganic materials 0.000 claims abstract description 8
- 239000004328 sodium tetraborate Substances 0.000 claims abstract description 8
- 235000010339 sodium tetraborate Nutrition 0.000 claims abstract description 8
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 4
- 230000003078 antioxidant effect Effects 0.000 claims abstract description 4
- 235000006708 antioxidants Nutrition 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 24
- 239000000470 constituent Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 17
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000002245 particle Substances 0.000 claims description 11
- 235000010288 sodium nitrite Nutrition 0.000 claims description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052796 boron Inorganic materials 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 159000000003 magnesium salts Chemical class 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000011347 resin Substances 0.000 claims 1
- 229920005989 resin Polymers 0.000 claims 1
- 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 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 239000004484 Briquette Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 238000005275 alloying Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 229910000616 Ferromanganese Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000001639 boron compounds Chemical class 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/242—Binding; Briquetting ; Granulating with binders
- C22B1/243—Binding; Briquetting ; Granulating with binders inorganic
-
- 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
- C04B18/00—Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B18/02—Agglomerated materials, e.g. artificial aggregates
- C04B18/021—Agglomerated materials, e.g. artificial aggregates agglomerated by a mineral binder, e.g. cement
-
- 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
- C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
- C04B28/24—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing alkyl, ammonium or metal silicates; containing silica sols
- C04B28/26—Silicates of the alkali metals
-
- 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
- C04B32/00—Artificial stone not provided for in other groups of this subclass
- C04B32/005—Artificial stone obtained by melting at least part of the composition, e.g. metal
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
- C22B1/00—Preliminary treatment of ores or scrap
- C22B1/14—Agglomerating; Briquetting; Binding; Granulating
- C22B1/24—Binding; Briquetting ; Granulating
- C22B1/242—Binding; Briquetting ; Granulating with binders
- C22B1/244—Binding; Briquetting ; Granulating with binders organic
-
- 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
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/0087—Uses not provided for elsewhere in C04B2111/00 for metallurgical applications
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Environmental & Geological Engineering (AREA)
- Geology (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Civil Engineering (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Metallurgy (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture And Refinement Of Metals (AREA)
- Fertilizers (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Abstract
The invention concerns agglomerating or briquetting of a mineral in fine granular state of less than 5 mm for smelting which may be mixed with fines by conglomerating the mineral with a binder prepared from at least sodium silicate, acrylic resin, vinyl alcohol, borax, magnesium chloride and if required during smelting an anti-oxidant such as sodium. The bound conglomerates or briquettes have superior strength properties.
Description
c WO 99!60175 PCTlZA99/00034 _j_ CONGLOMERATION OF MINERALS FROM A GRANULAR STATE WITH BINDER INCLUDING
WATERGLASS, ACRYLIC RESIN AND VINYL ALCOHOL
FIELD OF THE INVENTION
This invention relates to the conglomeration of minerals, excluding carbonaceous minerals, from a granular state and more particularly but not exclusively from granules of less than 5.0 mm granule size mixed with fines.
BACKGROUND TO THE INVENTION
Many minerals are recovered from ore in a state which makes them difficult to handle, transport and use in further processing. Of particular interest in this regard may be mentioned chrome ore where many mines have large dumps of this material in fine granular form.
OBJECT OF THE INVENTION
a is the object of the present invention to provide ,~ method of conglomerating minerals in this state and the binder for use in this method.
The term "minerals" in this specification is to b~e understood as excluding carbonaceous material.
SUMMARY OF THE INVENTION
s According to this invention there is provided a method of conglomerating a mineral in a granular state for smelting comprising admixing with the mineral an amount of 0.1% to 5% by mass of a binder including at least sodium silicate, acrylic resin, vinyl alcohol, an effective amount of a boron accelerator, a ~ magnesium salt and an anti-oxidant where nf;cessary for smelting and consolidating the mixture into discreet units suitable for transport and handling.
The boron accelerator may be borax and the magnesium salt may be magnesium chloride.
Further features of this invention provide for appropriate compounds present in the mineral to be conglomerated to be effective constituents in the determination of a binder for a specific mineral for the accelerator t~o be a boron compound and for the pH of the binder to be maintained at a pH of between 8.5 and 8.5.
Still further features of this invention provide for the conglomeration to be effected on a mineral having a particle size of less than 1.5 mm or a mixture of particle ~ 5 sizes in the range of 1.5 mm to 5.0 mm and fines, for the binder to be used at least in part in liquid form, for the accelerator to be used in dry or low viscosity liquid form and for remaining constituents to be used in high viscosity liquid form.
The invention also provides for the mixing to be effected at ambient or elevated temperature using a ribbon or other suitable blender and for the conglomeration to take place at elevated temperature and to be effected through heated moulds.
Still further features of this invention provide for the discreet units to be blocks or briquettes and for the units to have a size suitable for easy handling and transportation preferably having a weight of between 50 g and 1 kg.
The binder will preferably comprise constituents in thf; ratio Sodium silicate 1% to 30%
Acrylic resin 1 % to 30%
Vinyl alcohol 1 % to 20%
Borax 0.1 % to 15%
Magnesium chloride 0.1 % to 10%
Sodium nitrite 0.1%to 10%
by mass and have a pH of 6.5 to 8.5.
a . ' WO 99160175 PCT/ZA99/00034 The invention also provides for the conglomeration to be effected under pressure of approximately 14 000 KPA with a moisture content of less than 6% by weight in a briquetting machine.
Yet further features of this invention provide for the accelerator to be controlled by means of a buffer which is weak acidic or alkali.
Preferred embodiments of the invention are described by way of examples below.
In a first example of this invention chrome granules of an average particle size of 1.55 mm (10 microns - 2 mm) were mixed in a ribbon blender at room temperature for 3 minutes with a binder consisting of 1 o Sodium silicate 10%
Acrylic resin 4%
Vinyl alcohol 10%
Borax 1 Magnesium chloride 3%
Sodium nitrite 1 The constituents were mixed in water and in the percE;ntages given by mass.
Samples were conglomerated using a Komarek briquetting press under a pressure of approximately 14000 KPA.
The briquettes are exceptionally hard and on comprE;ssion testing were found to 2 o have a compression strength of 27.0 KPA.
In a second example manganese granules of a similar size to those of the chrome in the first example given above were sirniiarly mixed with the same binder.
The mixture was conglomerated in the same manner as the chrome and the resulting briquettes were found to have a compressive strength of 48.3 KPA.
In both examples the moisture content of the briquettes was kept below 4% by mass.
' WO 99/60175 PCTIZA99100034 The briquettes maintained their integrity at a temperature in excess of 1500°C.
Trials on a practical scale were conducted in a 100 ton mineral briquetting trial.
The mineral was obtained from the Meyerton area of Gauteng, South Africa and had a particle size range of 10 microns to 2 mm.
The equipment used was that specified above.
The binder consisted of Sodium silicate 10% as a 20% solution Acrylic resin 4% as a 46°~ solution Vinyl alcohol 10°~ as a 10% solution t o Borax 0.8%
Magnesium chloride 2.5°~
and was used as a mixture of 6% by weight with water to give an overall water content of 4.5%. The accelerator was added as dry powder.
The material was briquetted in batches of 1.4 tons of silica manganese mixed with 'l000 grams of dry borax accelerator with the remainder of the binder being a thick slurry. The mixing time in the ribbon blender vuas five minutes and the pressure in the briquetttng machine was 23 Mpa.
Representative results were as follows:-Result Green Cured abrasion indices Cured crushing Weathered strength (°~) strength crushing (Number Spec > 75% Spec < 10°k strength of drops (pellets survived) still wet) Tumbler 1 Tumbter 2 Ml~a kq,lbric~ kgJbriq 2 5 Good briquettes 1.6 60.2 24.3 1.549 62.7 36.4 Good briquettes 2.0 - - 1.373 55.7 -Good 3 0 briquettes 2.8 - - 1.912 77.37 -Good briquettes 3.2 56.5 28.9 1.453 58.8 42.1 Similar results obtained using a ferromanganese ore and the same binder were:-Result Green Cured abrasion indicesCured crushing Weathered strength (~) strength crushing {Number Spec> 75% Spec < 10% strength of drops (pellets survived) still wetL
Tumbler 1 Tumbler M,pa kg,/bri~kq /brig Good briquettes - - - 2.123 85.9 -Good briquettes 3.8 10.3 48.7 1.639 66.3 33.3 Good briquettes 3.2 - - 1.800 71.3 Good ~ 5 briquettes 3.0 - 1.800 71.3 -Good briquettes 2.6 - - 1.137 46 -Good briquettes 1.8 8 40:2 1.197 48.4 20.6 The briquettes were introduced into a furnace process wherein the furnace was not shrouded against ambient atmosphere. No violent reaction took place and the results of the alloying process were satisfactory.
The binder did not affect the properties of the minE;rals and affords some advantage to the smelting process. No anti-oxidant was required in the binder because the smelting furnace contents were shielded against oxidation.
It will be appreciated that the composition of the binder can be varied to obtain the best results with each mineral to be agglomerated. 'The most suitable recipe can be determined with reasonable experimentation and a comprehensive analysis of the minerals.
3 o The constituents of the binder do not only conglomerate the mineral; they are selected also to have only desirable effects on the final alloy. The organic components are chosen for insolubility in the metal and become constituents in the furnace slag.
i i:
The organic constituents will also be chosen from food quality products to avoid contamination in that no toxic reaction products result from the use of the binder.
The inclusion of sodium silicate gives the final briquette the required resistance to temperature. It also, along with the magnesium chloride gives the product insolubility in water and thus good weathering characteristics.
The polyvinyl alcohol and acrylic resin combination gives hardness and insolubility to the final product enabling it to melt inwardly in use and the small quantities of binder required make it easy to prepare and handle. The basic binding appear to be that between mineral and polyvinyl alcohol. It is necessary that the latter be dissolved in the water during rnixing and good stirring is required. Sometimes elevated temperature of the wvater will materially assist in reducing the mixing time required.
The binder lends itself to a wide range of constituent composition for achieving conglomeration in the most economic manner with respect both to time and composition of the binder.
The sodium nitrite constituent acts to prevent oxidation and thus dilution of constituents such as manganese as alloying elements in the final metallurgical product. Where this product is produced in an argon shrouded furnace this constituent may be omitted from the binder.
2o It will further be understood that if particular circumstance relating to the mineral to be conglomerated so dictate the water content of the mixture prior to introduction into the consolidating moulds may bES more or less than the 6 percent referred to. Of course all water of crystalisation in the binder constituents will form part of overall moisture content under consideration.
This will determine to some extent how the binder is mixed. The accelerator may be used dry or as a low viscosity slurry. This enables control over the accelerator to be maintained at a high level.
Always optimum mixing conditions will be determined by the mineral to be conglomerated and the use to which it is to be put. 'The best binder composition 3 o can be determined especially based on a detailecl knowledge of the mineral composition.
_7_ Those skilled in the art will appreciate that the binder constituents are largely determined by the final water content that can be tolerated in the conglomerated unit. This content is also effected by the costs aspects of the briquette composition where the costs of removing moisture from the mineral must be weighed against the difficulty of using binder constituents with minimum water contest.
In particular the degree of saponification of the vinyl alcohol to a large extent affects the difficulty in dissolution and temperature and times needed for this process. Thus the pH control can also becorr~e important to prevent the reaction of binder constituents from taking place too rapidly when the binder is mixed into the mineral. Here the use of a buffer preferably citric acid or potassium hydroxide, chosen for a binder of a specific mineral, will also assist in the control of the binder reaction.
Further the physical characteristic of the mineral is important. Larger sized particles can be accommodated provided there is an adequate quantity of fines between the larger particles. Mixtures of this kincl will require the use of less binder material and the optimum dosage rate will be proportional to the distribution of particle sizes in the mineral.
A very suitable proportionality of particle size is 1.5 mm to 2 mm - 20% by weight;
.8 mm to 1 mm - 30% by weight with the remainder as. powder.
As mentioned above the sodium nitrite may be omitted when the briquettes are used in a shrouded furnace. However this constituent, or an equivalent, may beneficially be included in the binder as a preservative where there is a possibility of the briquettes or blocks being stored for lengthy periods of time.
It will also be understood that the mineral may be bound into blocks rather than briquettes. This will enable mineral having larger size particles than those referred to above and a wider size range to be acconnmodated with the binder of this invention. Equipment suitable for this purpose is commercially available.
WATERGLASS, ACRYLIC RESIN AND VINYL ALCOHOL
FIELD OF THE INVENTION
This invention relates to the conglomeration of minerals, excluding carbonaceous minerals, from a granular state and more particularly but not exclusively from granules of less than 5.0 mm granule size mixed with fines.
BACKGROUND TO THE INVENTION
Many minerals are recovered from ore in a state which makes them difficult to handle, transport and use in further processing. Of particular interest in this regard may be mentioned chrome ore where many mines have large dumps of this material in fine granular form.
OBJECT OF THE INVENTION
a is the object of the present invention to provide ,~ method of conglomerating minerals in this state and the binder for use in this method.
The term "minerals" in this specification is to b~e understood as excluding carbonaceous material.
SUMMARY OF THE INVENTION
s According to this invention there is provided a method of conglomerating a mineral in a granular state for smelting comprising admixing with the mineral an amount of 0.1% to 5% by mass of a binder including at least sodium silicate, acrylic resin, vinyl alcohol, an effective amount of a boron accelerator, a ~ magnesium salt and an anti-oxidant where nf;cessary for smelting and consolidating the mixture into discreet units suitable for transport and handling.
The boron accelerator may be borax and the magnesium salt may be magnesium chloride.
Further features of this invention provide for appropriate compounds present in the mineral to be conglomerated to be effective constituents in the determination of a binder for a specific mineral for the accelerator t~o be a boron compound and for the pH of the binder to be maintained at a pH of between 8.5 and 8.5.
Still further features of this invention provide for the conglomeration to be effected on a mineral having a particle size of less than 1.5 mm or a mixture of particle ~ 5 sizes in the range of 1.5 mm to 5.0 mm and fines, for the binder to be used at least in part in liquid form, for the accelerator to be used in dry or low viscosity liquid form and for remaining constituents to be used in high viscosity liquid form.
The invention also provides for the mixing to be effected at ambient or elevated temperature using a ribbon or other suitable blender and for the conglomeration to take place at elevated temperature and to be effected through heated moulds.
Still further features of this invention provide for the discreet units to be blocks or briquettes and for the units to have a size suitable for easy handling and transportation preferably having a weight of between 50 g and 1 kg.
The binder will preferably comprise constituents in thf; ratio Sodium silicate 1% to 30%
Acrylic resin 1 % to 30%
Vinyl alcohol 1 % to 20%
Borax 0.1 % to 15%
Magnesium chloride 0.1 % to 10%
Sodium nitrite 0.1%to 10%
by mass and have a pH of 6.5 to 8.5.
a . ' WO 99160175 PCT/ZA99/00034 The invention also provides for the conglomeration to be effected under pressure of approximately 14 000 KPA with a moisture content of less than 6% by weight in a briquetting machine.
Yet further features of this invention provide for the accelerator to be controlled by means of a buffer which is weak acidic or alkali.
Preferred embodiments of the invention are described by way of examples below.
In a first example of this invention chrome granules of an average particle size of 1.55 mm (10 microns - 2 mm) were mixed in a ribbon blender at room temperature for 3 minutes with a binder consisting of 1 o Sodium silicate 10%
Acrylic resin 4%
Vinyl alcohol 10%
Borax 1 Magnesium chloride 3%
Sodium nitrite 1 The constituents were mixed in water and in the percE;ntages given by mass.
Samples were conglomerated using a Komarek briquetting press under a pressure of approximately 14000 KPA.
The briquettes are exceptionally hard and on comprE;ssion testing were found to 2 o have a compression strength of 27.0 KPA.
In a second example manganese granules of a similar size to those of the chrome in the first example given above were sirniiarly mixed with the same binder.
The mixture was conglomerated in the same manner as the chrome and the resulting briquettes were found to have a compressive strength of 48.3 KPA.
In both examples the moisture content of the briquettes was kept below 4% by mass.
' WO 99/60175 PCTIZA99100034 The briquettes maintained their integrity at a temperature in excess of 1500°C.
Trials on a practical scale were conducted in a 100 ton mineral briquetting trial.
The mineral was obtained from the Meyerton area of Gauteng, South Africa and had a particle size range of 10 microns to 2 mm.
The equipment used was that specified above.
The binder consisted of Sodium silicate 10% as a 20% solution Acrylic resin 4% as a 46°~ solution Vinyl alcohol 10°~ as a 10% solution t o Borax 0.8%
Magnesium chloride 2.5°~
and was used as a mixture of 6% by weight with water to give an overall water content of 4.5%. The accelerator was added as dry powder.
The material was briquetted in batches of 1.4 tons of silica manganese mixed with 'l000 grams of dry borax accelerator with the remainder of the binder being a thick slurry. The mixing time in the ribbon blender vuas five minutes and the pressure in the briquetttng machine was 23 Mpa.
Representative results were as follows:-Result Green Cured abrasion indices Cured crushing Weathered strength (°~) strength crushing (Number Spec > 75% Spec < 10°k strength of drops (pellets survived) still wet) Tumbler 1 Tumbter 2 Ml~a kq,lbric~ kgJbriq 2 5 Good briquettes 1.6 60.2 24.3 1.549 62.7 36.4 Good briquettes 2.0 - - 1.373 55.7 -Good 3 0 briquettes 2.8 - - 1.912 77.37 -Good briquettes 3.2 56.5 28.9 1.453 58.8 42.1 Similar results obtained using a ferromanganese ore and the same binder were:-Result Green Cured abrasion indicesCured crushing Weathered strength (~) strength crushing {Number Spec> 75% Spec < 10% strength of drops (pellets survived) still wetL
Tumbler 1 Tumbler M,pa kg,/bri~kq /brig Good briquettes - - - 2.123 85.9 -Good briquettes 3.8 10.3 48.7 1.639 66.3 33.3 Good briquettes 3.2 - - 1.800 71.3 Good ~ 5 briquettes 3.0 - 1.800 71.3 -Good briquettes 2.6 - - 1.137 46 -Good briquettes 1.8 8 40:2 1.197 48.4 20.6 The briquettes were introduced into a furnace process wherein the furnace was not shrouded against ambient atmosphere. No violent reaction took place and the results of the alloying process were satisfactory.
The binder did not affect the properties of the minE;rals and affords some advantage to the smelting process. No anti-oxidant was required in the binder because the smelting furnace contents were shielded against oxidation.
It will be appreciated that the composition of the binder can be varied to obtain the best results with each mineral to be agglomerated. 'The most suitable recipe can be determined with reasonable experimentation and a comprehensive analysis of the minerals.
3 o The constituents of the binder do not only conglomerate the mineral; they are selected also to have only desirable effects on the final alloy. The organic components are chosen for insolubility in the metal and become constituents in the furnace slag.
i i:
The organic constituents will also be chosen from food quality products to avoid contamination in that no toxic reaction products result from the use of the binder.
The inclusion of sodium silicate gives the final briquette the required resistance to temperature. It also, along with the magnesium chloride gives the product insolubility in water and thus good weathering characteristics.
The polyvinyl alcohol and acrylic resin combination gives hardness and insolubility to the final product enabling it to melt inwardly in use and the small quantities of binder required make it easy to prepare and handle. The basic binding appear to be that between mineral and polyvinyl alcohol. It is necessary that the latter be dissolved in the water during rnixing and good stirring is required. Sometimes elevated temperature of the wvater will materially assist in reducing the mixing time required.
The binder lends itself to a wide range of constituent composition for achieving conglomeration in the most economic manner with respect both to time and composition of the binder.
The sodium nitrite constituent acts to prevent oxidation and thus dilution of constituents such as manganese as alloying elements in the final metallurgical product. Where this product is produced in an argon shrouded furnace this constituent may be omitted from the binder.
2o It will further be understood that if particular circumstance relating to the mineral to be conglomerated so dictate the water content of the mixture prior to introduction into the consolidating moulds may bES more or less than the 6 percent referred to. Of course all water of crystalisation in the binder constituents will form part of overall moisture content under consideration.
This will determine to some extent how the binder is mixed. The accelerator may be used dry or as a low viscosity slurry. This enables control over the accelerator to be maintained at a high level.
Always optimum mixing conditions will be determined by the mineral to be conglomerated and the use to which it is to be put. 'The best binder composition 3 o can be determined especially based on a detailecl knowledge of the mineral composition.
_7_ Those skilled in the art will appreciate that the binder constituents are largely determined by the final water content that can be tolerated in the conglomerated unit. This content is also effected by the costs aspects of the briquette composition where the costs of removing moisture from the mineral must be weighed against the difficulty of using binder constituents with minimum water contest.
In particular the degree of saponification of the vinyl alcohol to a large extent affects the difficulty in dissolution and temperature and times needed for this process. Thus the pH control can also becorr~e important to prevent the reaction of binder constituents from taking place too rapidly when the binder is mixed into the mineral. Here the use of a buffer preferably citric acid or potassium hydroxide, chosen for a binder of a specific mineral, will also assist in the control of the binder reaction.
Further the physical characteristic of the mineral is important. Larger sized particles can be accommodated provided there is an adequate quantity of fines between the larger particles. Mixtures of this kincl will require the use of less binder material and the optimum dosage rate will be proportional to the distribution of particle sizes in the mineral.
A very suitable proportionality of particle size is 1.5 mm to 2 mm - 20% by weight;
.8 mm to 1 mm - 30% by weight with the remainder as. powder.
As mentioned above the sodium nitrite may be omitted when the briquettes are used in a shrouded furnace. However this constituent, or an equivalent, may beneficially be included in the binder as a preservative where there is a possibility of the briquettes or blocks being stored for lengthy periods of time.
It will also be understood that the mineral may be bound into blocks rather than briquettes. This will enable mineral having larger size particles than those referred to above and a wider size range to be acconnmodated with the binder of this invention. Equipment suitable for this purpose is commercially available.
Claims (17)
1. A method of conglomerating a mineral in a granular state for smelting characterised in that the minerals are admixed with an amount of 0.1 % to 5% by mass of a binder including at least sodium silicate, acrylic resin, vinyl alcohol, an effective amount of boron containing compound as an accelerator, magnesium salt and an anti-oxidant where necessary for smelting, and conglomerating the mixture.
2. A process as claimed in claim 1 characterised in that the mineral has a particle size of less than 5 mm and contains fines.
3. A process as claimed in claim 2 characterised in that the mineral is in the form of a mixture of particle sizes ranging from 1.5mm to 2 mm and contains fines.
4. A process as claimed in any one of the preceding claims characterised in that appropriate compounds present in the mineral are effective constituents in the determination of a mineral specific binder.
5. A process as claimed in any one of the preceding claims characterised in that the pH of the binder is maintained between 6.5 and 8.5.
6. A process as claimed in any one of the preceding claims characterised in that the accelerator is controlled by the addition of a buffer which is weak acid or alkali.
7. A process as claimed in any one of the preceding claims characterised in that at least the resin and alcohol are mixed in water in a quantity dependant on the water content permissable in the finally conglomerated mineral.
8. A process as claimed in claim 7 characterised in that the water is added at an elevated temperature.
9. A process as claimed in any one of the preceding claims characterised in that conglomeration is effected under pressure of at least 12 000 KPA.
10. A process as claimed in any once of the preceding claims characterised in that the moisture content of the mixture fed for conglomeration is less than 6% by weight.
11. A process as claimed in any one of the preceding claims characterised in that the conglomeration is effected at elevated temperature.
12. A process as claimed in claim 11 characterised in that the conglomeration is effected in heated moulds.
13. A process as claimed in any one of the preceding claims characterised in that the binder comprises constituents in the ratio Sodium silicate 1% to 30%
Acrylic resin 1% to 30%
Vinyl alcohol 1% to 20%
Borax 0.1% to 15%
Magnesium chloride 0.1% to 10%
Sodium nitrite 0.1% to 10%
by mass.
Acrylic resin 1% to 30%
Vinyl alcohol 1% to 20%
Borax 0.1% to 15%
Magnesium chloride 0.1% to 10%
Sodium nitrite 0.1% to 10%
by mass.
14. A process as claimed in claim 13 characterised in that the binder consists of constituents in the ratio Sodium silicate 8% - 12%
Acrylic resin 2% - 5%
Vinyl alcohol 8% - 12%
Borax .6% - 1.1%
Magnesium chloride 2.5% - 3.1%
Sodium nitrite .8% - 1.2%
by mass.
Acrylic resin 2% - 5%
Vinyl alcohol 8% - 12%
Borax .6% - 1.1%
Magnesium chloride 2.5% - 3.1%
Sodium nitrite .8% - 1.2%
by mass.
15. A process as claimed in any one of the preceding claims characterised in that this mixture is consolidated into discreet units suitable for handling and transport.
16. A process as claimed in claim 15 characterised in that the mixture is consolidated into briquettes or blocks.
17. A binder for a process as claimed in any one of the preceding claims characterised in that it includes the constituents as defined in claims 1, 3, 13 or 14.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ZA984152 | 1998-05-18 | ||
| ZA98/4152 | 1998-05-18 | ||
| PCT/ZA1999/000034 WO1999060175A1 (en) | 1998-05-18 | 1999-05-17 | Conglomeration of minerals from a granular state with binder including waterglass, acrylic resin and vinyl alcohol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2332797A1 true CA2332797A1 (en) | 1999-11-25 |
Family
ID=25587010
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002332797A Abandoned CA2332797A1 (en) | 1998-05-18 | 1999-05-17 | Conglomeration of minerals from a granular state with binder including waterglass, acrylic resin and vinyl alcohol |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP1080237A1 (en) |
| JP (1) | JP2002515546A (en) |
| AU (1) | AU4103199A (en) |
| BR (1) | BR9910561A (en) |
| CA (1) | CA2332797A1 (en) |
| NO (1) | NO20005789L (en) |
| PL (1) | PL344292A1 (en) |
| TR (1) | TR200003388T2 (en) |
| WO (1) | WO1999060175A1 (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5643600A (en) * | 1999-06-03 | 2000-12-28 | Nu-Rock International Limited | Process of agglomerating particulate waste material |
| RU2198940C1 (en) * | 2001-07-03 | 2003-02-20 | Закрытое акционерное общество "Консультационная компания "КОНВЕСТ" | Method of production of briquettes from finely- dispersed oxides of metals |
| CA2499146A1 (en) * | 2002-09-18 | 2004-04-15 | Akzo Nobel Nv | Binder composition and process for agglomerating particulate material |
| BR0301250A (en) * | 2003-05-05 | 2004-12-21 | Samarco Mineracao Sa | Iron ore pellets with reduced abrasion, bonding, degradation and dust emission, and their manufacturing process |
| AP2012006296A0 (en) * | 2009-11-17 | 2012-06-30 | Vale Sa | Ore fine agglomerate to be used in sintering process and production process of ore fines agglomerate. |
| CN104975171A (en) * | 2015-05-28 | 2015-10-14 | 营口市林合茂科技开发有限公司 | Boric sludge pellet binder/iron smelting auxiliary and preparation method of boric sludge pellet binder/iron smelting auxiliary |
| FI20165401A (en) * | 2016-05-11 | 2017-11-12 | Kemira Oyj | Binder composition and sintering process |
| GB201613915D0 (en) | 2016-08-15 | 2016-09-28 | Binding Solutions Ltd | Briquettes |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA762272B (en) * | 1976-05-23 | 1977-07-27 | Samancor Management Services | Method for forming ore cakes |
| JPS608284B2 (en) * | 1977-03-10 | 1985-03-01 | 電気化学工業株式会社 | Manufacturing method of briquettes for modified carburizers |
| ZA776166B (en) * | 1977-10-17 | 1978-12-27 | Revertex Ltd | The treatment of particulate material to form aggregates |
| US4167398A (en) * | 1978-03-13 | 1979-09-11 | American Colloid Company | Carbonaceous briquette and method for making same |
| JPS5547332A (en) * | 1978-09-29 | 1980-04-03 | Yokohamashi | Solidifying treatment of electrostatic precipitation ash |
| AU546359B2 (en) * | 1980-12-08 | 1985-08-29 | Revertex (South Africa) Pty. Ltd. | Briquetting of particulate materials |
| JPS58204093A (en) * | 1982-05-24 | 1983-11-28 | Kozai Gijutsu Kenkyusho:Kk | Solid fufl |
| DE3445503A1 (en) * | 1984-12-13 | 1986-06-19 | Woellner-Werke GmbH & Co, 6700 Ludwigshafen | Process for producing briquettes |
| SU1622515A1 (en) * | 1987-07-30 | 1991-01-23 | Специализированный проектно-изыскательский институт "Гидроспецпроект" | Method of consolidating ground |
| US4751259A (en) * | 1987-08-05 | 1988-06-14 | Nalco Chemical Company | Compositions for iron ore agglomeration |
| DD299875A7 (en) * | 1989-09-29 | 1992-05-14 | Kali Veb K | METHOD FOR THE PRODUCTION OF BRIKETTABLE MGO STRUCTURES |
| NO170626C (en) * | 1990-05-18 | 1992-11-11 | Norsk Proco As | NON-PROTECTED, WATERPROOF AND ACID RESISTANT PRODUCT |
| US5738694A (en) * | 1994-01-21 | 1998-04-14 | Covol Technologies, Inc. | Process for recovering iron from iron-containing material |
| US5589118A (en) * | 1994-01-21 | 1996-12-31 | Covol Technologies, Inc. | Process for recovering iron from iron-containing material |
| US5453103A (en) * | 1994-01-21 | 1995-09-26 | Environmental Technologies Group International, Inc. | Reclaiming and utilizing discarded and newly formed coke breeze, coal fines, and blast furnace revert materials, and related methods |
-
1999
- 1999-05-17 EP EP99924556A patent/EP1080237A1/en not_active Withdrawn
- 1999-05-17 WO PCT/ZA1999/000034 patent/WO1999060175A1/en not_active Ceased
- 1999-05-17 CA CA002332797A patent/CA2332797A1/en not_active Abandoned
- 1999-05-17 AU AU41031/99A patent/AU4103199A/en not_active Abandoned
- 1999-05-17 PL PL99344292A patent/PL344292A1/en not_active Application Discontinuation
- 1999-05-17 TR TR2000/03388T patent/TR200003388T2/en unknown
- 1999-05-17 BR BR9910561-6A patent/BR9910561A/en not_active Application Discontinuation
- 1999-05-17 JP JP2000549780A patent/JP2002515546A/en active Pending
-
2000
- 2000-11-15 NO NO20005789A patent/NO20005789L/en not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| WO1999060175A1 (en) | 1999-11-25 |
| BR9910561A (en) | 2001-01-30 |
| AU4103199A (en) | 1999-12-06 |
| NO20005789D0 (en) | 2000-11-15 |
| TR200003388T2 (en) | 2001-02-21 |
| NO20005789L (en) | 2001-01-18 |
| EP1080237A1 (en) | 2001-03-07 |
| PL344292A1 (en) | 2001-10-22 |
| JP2002515546A (en) | 2002-05-28 |
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