AU655514B2 - Process for manufacturing a refractory body - Google Patents
Process for manufacturing a refractory body Download PDFInfo
- Publication number
- AU655514B2 AU655514B2 AU28526/92A AU2852692A AU655514B2 AU 655514 B2 AU655514 B2 AU 655514B2 AU 28526/92 A AU28526/92 A AU 28526/92A AU 2852692 A AU2852692 A AU 2852692A AU 655514 B2 AU655514 B2 AU 655514B2
- Authority
- AU
- Australia
- Prior art keywords
- microns
- process according
- ironsand
- less
- mixture
- 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.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims description 30
- 230000008569 process Effects 0.000 title claims description 28
- 238000004519 manufacturing process Methods 0.000 title description 8
- 239000000463 material Substances 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 26
- 239000011449 brick Substances 0.000 claims description 21
- 239000004927 clay Substances 0.000 claims description 16
- 238000003825 pressing Methods 0.000 claims description 13
- 239000004115 Sodium Silicate Substances 0.000 claims description 11
- 239000012141 concentrate Substances 0.000 claims description 11
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 11
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 11
- 239000000243 solution Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 238000010304 firing Methods 0.000 claims description 9
- 238000005245 sintering Methods 0.000 claims description 9
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 8
- HPTYUNKZVDYXLP-UHFFFAOYSA-N aluminum;trihydroxy(trihydroxysilyloxy)silane;hydrate Chemical compound O.[Al].[Al].O[Si](O)(O)O[Si](O)(O)O HPTYUNKZVDYXLP-UHFFFAOYSA-N 0.000 claims description 7
- 229910052621 halloysite Inorganic materials 0.000 claims description 7
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 6
- 239000001569 carbon dioxide Substances 0.000 claims description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 4
- 238000007493 shaping process Methods 0.000 claims description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
- 239000005642 Oleic acid Substances 0.000 claims description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- 238000011160 research Methods 0.000 claims description 2
- 239000003921 oil Substances 0.000 claims 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 14
- 238000005338 heat storage Methods 0.000 description 10
- 238000005336 cracking Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000008646 thermal stress Effects 0.000 description 4
- 239000000919 ceramic Substances 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- 229910052595 hematite Inorganic materials 0.000 description 2
- LIKBJVNGSGBSGK-UHFFFAOYSA-N iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Fe+3].[Fe+3] LIKBJVNGSGBSGK-UHFFFAOYSA-N 0.000 description 2
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229910052611 pyroxene Inorganic materials 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 206010000060 Abdominal distension Diseases 0.000 description 1
- 229910011255 B2O3 Inorganic materials 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910001583 allophane Inorganic materials 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000010427 ball clay Substances 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 208000024330 bloating Diseases 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- NWXHSRDXUJENGJ-UHFFFAOYSA-N calcium;magnesium;dioxido(oxo)silane Chemical compound [Mg+2].[Ca+2].[O-][Si]([O-])=O.[O-][Si]([O-])=O NWXHSRDXUJENGJ-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910021540 colemanite Inorganic materials 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052637 diopside Inorganic materials 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000011019 hematite Substances 0.000 description 1
- 230000006872 improvement Effects 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
- YDZQQRWRVYGNER-UHFFFAOYSA-N iron;titanium;trihydrate Chemical compound O.O.O.[Ti].[Fe] YDZQQRWRVYGNER-UHFFFAOYSA-N 0.000 description 1
- 229910052914 metal silicate Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 229910052664 nepheline Inorganic materials 0.000 description 1
- 239000010434 nepheline Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- -1 sodium Chemical compound 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000010435 syenite Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Description
I i i II I -P ll~l~ Our Ref: 450823 635514 P/00/011 Regulation 3:2
AUSTRALIA
Patents Act 1990
ORIGINAL
COMPLETE SPECIFICATION STANDARD PATENT Cc C
CCC;
C C I C SC C Cs
CC
S
Applicant(s): Industrial Research Limited Gracefield Road LOWER HUTT NEW ZEALAND DAVIES COLLISON CAVE Patent Trade Mark Attorneys Level 10, 10 Barrack Street SYDNEY NSW 2000 Address for Service: Invention Title: Process for manufacturing a refractory body The following statement is a full description of this invention, including the best method of performing it known to me:- 5020 The invention relates to a process for manufacturing refractory bodies, particularly heat storage bricks made from bonded ironsand or concentrates derived from ironsand.
Introduction Refractory or heat resistant bodies such as ceramtic bricks are characterised by a -high heat storage capacity and so are commonly used as a heat storage medium. The material from which they are made must have a high specific heat, and in order to achieve the maximum possible heat storage capacity within given diesos th rcs utas have the highest possible densty. Thi isbecase he eatstorage capacity per unit *.:Heat storage bricks are typically manufactured from iron oxides but at present all such bricks are imported into New Zealand, often in storage heaters. These imported bricks are S available in two grades having densities of 2.5 and 3.8 g cm- 3 respectively. They commonly contain mixtures of haematite and R magnetite, that is Fe 2 O, and Fe'O 4 but are prone to cracking and edge-chipping.
Oblect of the Invention The object of the przesent invention is to provide a process for manufacturing a refractory body having a high. heat storage capacity per unit volume which represents an improvement upon, or at least an alternative to, known processes.
Statement of the Invention The present invention comprises a process for manufacturing a refractory body comprising blending ironsand material and a pressing aid, shaping the mixture, and firing the shaped mixture to form said refractory body. "Ironsand" is a beach or dune sand containing iron-bearing minerals which are primarily titanomagnetite in this specification.
Preferably the ironsand material is titanomagnetite S. ironsand or reduced primary concentrate as herein defined. New Zealand North Island titanomagnetite ironsand has been found to S be a suitable base material for making refractory bricks with the process of the invention. The ironsand concentrate has a specific heat of greater than 0.20 cal.g- 1
.K
1 Both titanomagnetite ironsand and "reduced primary concentrate", that Sis iron-enriched material derived directly from titanomagnetite ironsand by reduction, are suitable.
C c When a single size fraction of ironsand material is used the refractory body will have a heat storage capacity per unit volume at least substantially equivalent to that of known refractory bodies such as heat storage bricks. Such a refractory body produced by the process of the invention with a single size fraction of from herein be referred to as a "basic brick".
2jY Preferably, the average grain size of the ironsand material is less than 140 microns, especially from substantially 110 microns to substantially 130 microns, and more especially substantially 120 microns.
Superior heat storage capacity per unit volume can be achieved, when two or more size fractions or ironsand material are used and from herein a refractory body made in that way will be referred to as an "optimised brick".
An optimised brick can be made using two size fractions of ironsand material. Preferably the first size fraction of the 0.
ironsand material has an average grain size of less than substantially 140 microns, especially from substantially 110 0 microns to substantially 130 microns, and more especially substantially 120 microns; and preferably the second size fraction of the ironsand material has an average grain size of less than substantially 60 microns, especially from substantially 20 microns to substantially 50 microns, and more especially substantially 34 microns.
*o« 6 ea Preferably the first size fraction of the ironsand material comprises unmilled magnetically separated titanomagnetite ironsand and the second size fraction comprises milled ironsand in a ratio of substantially 1:2 to substantially 2:1, especially substantially 2:3 to substantially 3:2, and more especially substantially 1:1 respectively.
3 An optimised brick can be made using three size fractions of ironsand material also. Preferably the first size fraction of the ironsand material has an average grain size of less than substantially 140 microns, especially from substantially 110 microns to substantially 130 microns, and more especially substantially 120 microns; and preferably the second size fraction of the ironsand material has an average grain size of less than substantially 100 microns, especially from substantially 20 microns to substantially 60 microns, and more especially substantially 34 microns; and preferably the third size fraction of the ironsand material has an average grain size of less than substantially 50 microns, especially less than Ssubstantially 10 microns, and more especially less than
S.:
S" substantially 1 micron.
Preferably the first size fraction of the ironsand S material comprises unmilled magnetically separated titanomagnetite ironsand, the second size fraction comprises coarsely milled ironsand, and the third size fraction comprises finely milled ironsand in a ratio of 15 to 25 15 to 25 1 respectively.
Preferably the pressing aid is a sodium silicate solution or a wet clay, such as a mixture of halloysite clay and water.
4 1' The use of a sintering aid is not essential but it is preferred especially if optimised rather than basic bricks are to be produced.
Sodium silicate solution, or a mixture of halloysite clay and water are preferred sintering aids.
If the blend of ironsand material includes an alkaline metal silicate solution the "green" or unfired strength of the mixture may then be increased prior to firing by exposing the mixture to gaseous carbon dioxide which in turn maximises the strength of the final product. This is disclosed in our New Zealand patent specification 212330 which is incorporated herein by reference.
Preferably the blended fractions are shaped by being pressed into a mould at a pressure greater than substantially MPa, especially greater than substantially 60 MPa, and more especially substantially 70 MPa, and fired at a temperature not exceeding substantially 1300°C.
Detailed Description The invention will now be particularly described with reference to the accompanying drawings: Fig. 1 illustrates the effect of temperature on the density of 25 mm diameter ceramic pellets, 5 i- Fig. 2 illustrates the effect of rod-milled ironsand on the density of 25 mm diameter ceramic pellets fired at different temperatures, and Fig. 3 illustrates the effect of pressure on the density of 25 mm diameter ceramic pellets fired at different temperatures.
We have found ironsand material such as titanomagnetite ironsand and reduced primary concentrate to be suitable material from which to manufacture refractory bodies such as bricks for eq C S storage heaters. Such ironsand material will from herein be described as simply "ironsand".
While, a "basic" brick can be produced using a single S size fraction of ironsand, the density and thus the heat storage S capacity per unit volume of a refractory body can be maximised .tt by manufacturing the body from material of a variety of particle sizes such that the spaces between large grains can be filled by S smaller grains. We describe such an improved brick as an "optimised" brick.
We have found that a combination of a first size fraction of separated ironsand having an average grain size of less than substantially 140 microns, especially from substantially 110 to substantially 130 microns, and more especially substantially 120 microns, and a second size fraction 6 of ironsand having an average grain size of less than substantially 60 microns, especially from substantially microns to substantially 50 microns, and more especially substantially 34 microns, gives optimal densities after firing when the fractions are blended in a proportion of substantially 1:2 to substantially 2:1, especially substantially 2:3 to substantially 3:2, and more especially substantially 1:1 respectively. Preferably the first fraction is unmilled ironsand and the second fraction is milled ironsand.
We have also found that a combination of a first size a.
w. fraction of magnetically separated ironsand having an average grain size of less than substantially 140 microns, especially from substantially 110 microns to substantially 130 microns, and more especially substantially 120 microns; a second size fraction of ironsand having an average grain size of less than substantially 100 microns, especially from substantially microns to substantially 60 microns, and more especially substantially 34 microns; and a third size fraction of ironsand having an average grain size of less than substantially a microns, especially less than substnntially 10 microns, and more especially less than substantially 1 micron, gives further optimised densities after firing when the fractions are blended in a proportion of 15 to 25 15 to 25 1 respectiveLy.
Preferably the first fraction is unmilled ironsand, the second fraction is coarsely milled ironsand, and the third fraction is finely milled ironsand.
i The third size fraction can be particularly useful to optimise the density when the average grain size is less than substantially 10 microns, and especially less than substantially 1 micron. In most instances small quantities, such as less than by weight, will be sufficient.
The effectiveness of the second fraction is shown in Fig. 2.
Using two or three fractions not only provides better packing in the green state but the finely milled ironsand .t fragments sinter more rapidly at temperatures below 1300C. Very S high densities can be achieved by using large proportions of finely milled ironsand but those mixtures often have low green densities and shrink greatly during firing, resulting in warping and cracking. It is therefore important to choose an appropriate *c Sironsand composition and balance the density against the degree of shrinkage.
The material can be milled by conventional processing such as ball milling or rod milling, wet or dry, but the exact ratio of unmilled: coarse milled: fine milled ironsand will depend on the specific particle size distributions achieved during milling which will depend on the facilities used. Optimal brick density can be achieved by carefully choosing the particle i sizes and proportions.
8 11. to than .ally than n in tter sand V.ery ;of rteen Late Iree ;aing :act li 11 ved .mal ,ale 5010
K
1 1.
r
I
The chemical compositions of the magnetically separated New Zealand North Island titanomagnetite ironsand and the reduced primary concentrate used. for the purposes of the present invention are summarized in Table 1. below.
Table 1: Chemical composition of magnetically separated ironsand and reducied primary concentrate. Values represent the percentage of total weight.
9 A .9 9 09 9 *0 .9 9 9 4.9 90 o 9 o9 99 9 09 Reduced JLJ. VAA I Elu 58.0 9 09 9', o 99 99 9 9.90.9 0 *9*099 9 0 9049 9 0 99 0 09 Fe (total) Fe (metallic) Ti G, A1 2 0 3 sio 2 MgO CaD MnO
V
2 05 8.0 4.0 3.4 3.0 0.8 0.6 0.6 0.1 YrAvCor 71.6 63.0 9.9 4.2 3.6 99 99 9 9 99 99 90 1.91 0.7 0.7 0.6 0.1.
*9 9' 9 A C. 0 9gE to'..
to 0 0 A 00 in process this will achieved I: (but no ex and alkali solution, Other shaped gr increase at orement, be advani excesive The mineral composition of the concentrate is sUmmxarised in Table 2.below.
reduced primary -9 i Table 2: Mineral composition of reduced primary concentrate (NT Evans, Iron and Steel Society of the AIME, 37th Conf: Chicago (1978) 122).
63% iron metal (Fe) 12% ilmenite (FeTiO,) 9% pyroxene (Ca(FeMg)Si 2
O
6 8% spinel ((FeMg)Al 2 4 6% magnetite-ulvospinel (Fe 3 0 4 -FesTiO.) 3% armalcolite ((FeMg)Ti0,) S* S When an optimised brick is required the first target i in processing is to achieve a high "green" or unfired density as this will assist in obtaining a high fired density. This is achieved by using an optimum amount of additional pressing aids I (but no excess). Clay powders, for example wet halloysite clay, and alkali metal silicate solutions, for example sodium silicate solution, have been found to be good in this respect.
Optionally, if sodium silicate solution is used, the shaped green body can be exposed to carbon dioxide gas to increase the green strength. This is discussed in our aforementioned New Zealand patent specification No 212330 and may be advantageous if the unfired bodies need to be handled excessively.
10 ^SStW"-' 11 i The term "alkali metal silicate" used herein includes silicates of sodium or potassium, particularly sodium, and chemical equivalents thereof. The alkali metal silicate is preferably added to the raw material mixture as a commercial aqueous solution which generally contains about 40-50% solid sodium silicate. However, if desired, the viscosity can be adjusted by adding a small amount (eg up to substantially of water to obtain the required consistency. Alternatively, but less preferably, the alkali metal silicate may be added in powdered form and water subsequently blended in.
Optionally as pressing agents oleic acid or engine oil may be used. Water can be used either alone or in association with clay or sodium silicate to improve the plasticity of the body and homogeneity of the distribution of the pressing aids.
4* 4 *c 4r *r 4 44 4 *r 4 4.
*4 4 4 A sintering aid can be used to assist the high temperature bonding process. It is not required to produce a basic brick but it is preferred in the production of optimised bricks. Suitable sintering aids include saturated aqueous sodium silicate solution, sodium silicate powder, ground waste glass, lead bisilicate, magnetite powder (FeO4), hematite powder (Fe 2
O
3 colemanite (CaB,0. 5H,O), borax (NaB 4 0 7 boric oxide feldspar, nepheline syenite, halloysitic clay, bentonite clay, allophane-rich clay, kaolinitic ball clay, milled quartz sand, and amorphous silica.
11 Both sodium silicate solution and clay/water have dual roles as sintering aids and pressing aids. Excellent results have been obtained using pyroxene materials such as diopside, which occurs naturally in ironsand.
The ironsand fractions, pressing aids and/or sintering aids are blended by art-known means to ensure homogeneity in their distribution, packed and then pressed into an appropriately shaped mould. The greater the pressure used, the higher the green and fired densities will be. This is shown in Fig 3. The use of higher pressures is also accompanied with less shrinkage and distortion on firing.
0 et The shaped unfired bodies are heated by art-known methods to temperatures in the range of 1100 0 C to 1350 0 C (most S preferably 1200-1300C). Within limits the greater the pressure v used, the higher the fired density will be. Excessive temperature causes the bodies to warp and can cause bloating depending on which pressing/sintering aids are chosen. Instead of using excessive temperature it is better to increase the effect of temperature on density is illustrated in Fig. 1.
The invention will now be described with reference to particular examples but which are not intended to limit the scope of the invention.
-12 Example 1 Unmilled ironsand having an estimated average grain size of 120 microns and New Zealand China Clays halloysite clay were blended in the ratio of 96:4 by weight with 6% water added.
The mixture was transferred to a die, spread uniformly and pressed to a pressure of at least 70 MPa. The shaped body was allowed to stand and dry to develop green strength. The body was then heated gradually by BIC per minute to 1250'C, allowed to soak for 2 hours, and then cooled in a similarly controlled manner to avoid cracking due to thermal stresses.
*,:Example 2 tnmilled ironsand having an estimated average grain size of 120 microns, partially milled ironsand having an estimated average grain size of 34 microns and New Zealand China Clays falloysite clay were blended in the ratio of 48:48t4 by weight with 6% added water. The mixture was transferred to a die, spread uniformly and pressed to a pressure of at least ::MPa. The shaped body was allowed to stand and dry to develop green strength. The body was then heated gradually by 5 0 C per *::*minute to 1250 0 C, allowed to soak for 2 hours, and then cooled in a similarly controlled manner to avoid cracking due to thermal stresses.
Example 3 Unmiled ironsand having an estimated average grain size of 120 microns, partially milled ironsand having an 13 estimated average grain size of 34 microns and New Zealand China Clays Halloysite clay were blended in the ratio of 48:48:4 by weight with 6% added water. The mixture wag transferred to a die, spread uniformly and pressed to a pressure of at least I MPa. The shaped body was prefired at 100-120 9 C for about 1 hour, heated gradually by 5 0 C per minute to 1250'C, allowed to soak for 2 hours, and then cooled in a similarly controlled manner to 'avoid cracking due to thermal stresses.
Example 4 Unmilled ironsand having an estimated average grain Ssize of 120 microns, milled reduced primary concentrate having an estimated grain size of 20 microns and Sodium silicate solution were blended in the ratio 60:34:6 by weight transferred to a die, spread uniformly, and pressed to a pressure of at least Mpa. The shaped body was then exposed to gaseous carbon dioxide for 2 minutes to harden the body, heated gradually by 5 0
C
per minute to 1200'C allowed to soak for 2 hours and then cooled in a similarly controlled manner to avoid cracking due to thermal stresses.
The foregoing describes the invention and preferred formns thereof. Alterations and modifications as will be obvious to those skilled in the art are intended to be incorporated within the scope of the invention as defined in the following claims.
-14-
Claims (17)
- 2. A process according to claim 1, wherein the ironsand material is titanomagnetite ironsand or a reduced primary concentrate thereof as herein defined. *o 3. A process according to claim 1 or 2 wherein the average grain size of the ironsand material is less than substantially 140 microns, optionally from substantially 110 microns to substantially 130 microns, and most preferably substantially 120 microns.
- 4. A process according to claim 1 or 2, wherein there are two size fractions of ironsand material. t
- 5. A process according to claim 4, wherein the average grain size of the first fraction is less than substantially 140 microns, optionally from substantially 110 microns to substantially 130 microns, and most preferably substantially 120 microns. 15 4 I.>L cS rfB
- 6. A process according to claim 5, wherein the average grain size of the second fraction is less than substantially microns, preferably from substantially 20 microns to substantially 50 microns, and most preferably substantially 34 microns.
- 7. A process according to any one of claims 4 to 6, wherein the ratio of the first and second fractions is substantially 1:2 to substantially 2:1 respectively, optionally from substantially 2:3 to substantially 3:2 respectively, and most preferably substantially 1:1. r t
- 8. A process according to claim 1 or 2, wherein there are at least three size fractions of ironsand material. t¢
- 9. A process according to claim 8, wherein the average grain S size of the first fraction is less than substantially 140 S microns, optionally from substantially 110 microns to S substantially 130 microns, and most preferably substantially 120 microns.
- 10. A process according to claim 8, wherein the average grain size of the second fraction is less than substantially 1003 microns, optionally from substantially 20 microns to substantially 60 microns and most preferably substantially 34 microns. -16 i:t
- 11. A process according to claim 8, wherein the average grain size of the third fraction is less than substantially 50 microns, optionally less than substantially 10 microns and most preferably less than substantially 1 micron.
- 12. A process according to any one of claims 8 to 11, wherein the ratio of the first, second and third fractions is substantially 10 to 25:10 to 25:1 respectively.
- 13. A process according to any preceding claim, wherein the pressing aid is selected from one or more of clay including halloysite clay, an alkali metal silicate solution, oleic acid, oil and water. p
- 14. A process according to claim 13, wherein the pressing aid is an alkali metal silicate solution and the mixture is exposed S. to gaseous carbon dioxide prior to firing to increase its green strength.
- 15. A process according to any preceding claim wherein the ironsand material and the pressing aid are blended with a sintering aid prior to the shaping and firing.
- 16. A process according to claim 15, wherein the sintering aid is selected from sodium silicate solution and a mixture of halloysite clay and water. 17 -r.rirr; ~iirmanxl----a---rril;-~
- 17. A process according to any one of claims 1 to 16 wherein the mixture is shaped by pressing the mixture into a mould, and wherein the mixture is exposed to a pressure greater than substantially 50 MPa, optionally greater than substantially MPa, and most preferably substantially 70 MPa.
- 18. A process according to any preceding claim, wherein the mixture is fired at a temperature from substantially 1100°C to substantially 1350 C and most preferably from substantially 1200°C to substantially 1300°C. 44*4
- 19. An optimised brick as herein defined when prepared by the Sprocess of any one of claims 5 to 18. 0 4 o e Dated this 1st day of August, 1994 INDUSTRIAL RESEARCH LIMITED By its Patent Attorneys DAVIES COLLISON CAVE 4*41 o• a* 4 4 *4 o ABSTRACT A process for manufacturinq a refractory body comprising blending ironsand material and a pressing aid, shaping the mixture, and firing the shaped mixture to form the refractory body. t. Ut U U USt U Ut U U .4 S I 4. Ut 54. I
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NZ24067491A NZ240674A (en) | 1991-11-20 | 1991-11-20 | Manufacturing a refractory body from ironsand and a pressing agent. |
| NZ240674 | 1991-11-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2852692A AU2852692A (en) | 1993-05-27 |
| AU655514B2 true AU655514B2 (en) | 1994-12-22 |
Family
ID=19923807
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU28526/92A Ceased AU655514B2 (en) | 1991-11-20 | 1992-11-20 | Process for manufacturing a refractory body |
Country Status (2)
| Country | Link |
|---|---|
| AU (1) | AU655514B2 (en) |
| NZ (1) | NZ240674A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017157835A1 (en) * | 2016-03-18 | 2017-09-21 | Höganäs Ab (Publ) | Powder metal composition for easy machining |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE184818T1 (en) * | 1994-10-13 | 1999-10-15 | Georg Fischer Disa As | CRACKED AND GRADED MAGNETITE ORE MOLDS AND COREES AND METHOD OF CASTING METAL USING SAME |
| AT413211B (en) * | 2002-02-27 | 2005-12-15 | Huemer Gmbh F | Heat storage composition containing magnetite, silica as alkali earth silicate, hematite and mineral fibers useful, especially in powder form, as storage blocks for night storage heaters for domestic houses and other buildings |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5871070A (en) * | 1981-10-21 | 1983-04-27 | Taoka Chem Co Ltd | Manufacture of porous elastic grinding wheel |
-
1991
- 1991-11-20 NZ NZ24067491A patent/NZ240674A/en unknown
-
1992
- 1992-11-20 AU AU28526/92A patent/AU655514B2/en not_active Ceased
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5871070A (en) * | 1981-10-21 | 1983-04-27 | Taoka Chem Co Ltd | Manufacture of porous elastic grinding wheel |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2017157835A1 (en) * | 2016-03-18 | 2017-09-21 | Höganäs Ab (Publ) | Powder metal composition for easy machining |
| CN108778570A (en) * | 2016-03-18 | 2018-11-09 | 霍加纳斯股份有限公司 | The powder metal composition being easily worked |
| JP2019512604A (en) * | 2016-03-18 | 2019-05-16 | ホガナス アクチボラグ (パブル) | Metal powder composition easy to cut |
| CN108778570B (en) * | 2016-03-18 | 2022-02-25 | 霍加纳斯股份有限公司 | Easily processable powder metal compositions |
| US12157935B2 (en) | 2016-03-18 | 2024-12-03 | Hoganas Ab (Publ) | Powder metal composition for easy machining |
Also Published As
| Publication number | Publication date |
|---|---|
| NZ240674A (en) | 1994-01-26 |
| AU2852692A (en) | 1993-05-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101105437B1 (en) | Recycling of Waste Mag Carbon Refractories | |
| KR19990007639A (en) | Ceramic composition using solid waste and its manufacturing method | |
| US9403728B2 (en) | Flame-retardant product and use thereof | |
| CN104496438B (en) | A kind of quartz sand ore mine tailing or silica sand ore deposit mine tailing base high-strength ceramic plate and preparation method thereof | |
| US5420087A (en) | Refractory or fireproof brick as tin bath bottom brick | |
| KR101283756B1 (en) | Chromina-alumina refractory | |
| EP0544913B1 (en) | Process for producing silica brick | |
| US4265845A (en) | Process for the production of a ceramic heat-retaining brick | |
| AU655514B2 (en) | Process for manufacturing a refractory body | |
| CN107207352A (en) | Method for manufacturing ceramic tiles by using coal combustion waste | |
| CN1116423A (en) | Quartz preforms for high temperature applications and methods for their production | |
| JP5608561B2 (en) | Fireproof ceramic mixture, fireproof ceramic molded body formed by the mixture and use thereof | |
| CN108516689B (en) | A kind of method for preparing microcrystalline foam glass from high silicon iron tailings and blast furnace slag | |
| JP2968166B2 (en) | Method of manufacturing silica brick | |
| JP2601129B2 (en) | Alumina-chromia castable refractory and precast block using it | |
| KR100504164B1 (en) | Manufacture of heat reserving materials using Cu-making slag | |
| US4999325A (en) | Rebonded fused brick | |
| JPH04114969A (en) | Nitride-bonded sic refractory material | |
| DD244547A1 (en) | CERAMIC MATERIAL | |
| JPH09227223A (en) | Production of free-cutting combined ceramics | |
| CN117383922B (en) | Low-temperature quick-firing ceramic tile based on industrial solid waste and preparation method thereof | |
| CN113480296A (en) | Modified refractory brick with high thermal shock stability | |
| CN1031936C (en) | Magnesia-chrome sand fettling material | |
| JP3496770B2 (en) | Silicon iron nitride and method for producing the same | |
| JPH11228242A (en) | Ramming material for induction furnace |