Patent Grant
6995105
The present invention relates to the use of water-soluble copolymers as claimed in claim 1 as fluidizers and/or setting retarders for refractory compositions comprising alumina cement, e.g. low cement castables (LCCs) or ultra low cement castables (ULCCs).
Fluidizers are generally organic or inorganic additives which reduce the water requirement (demand) of unshaped refractory compositions, in particular castables. Such fluidizers either improve the processibility of the refractory composition at a given water content or they enable the amount of water added to be reduced while maintaining the consistency of the composition.
Refractory compositions comprising alumina cement are ones in which a calcium aluminate cement (synonyms: alumina cement, high-alumina cement) function as hydraulic binder. These cements are based on Al2O3-rich calcium or barium (sometimes also strontium) aluminates and have an Al2O3 content of ≧35%. The classification of the cement content is determined by the content of CaO as hydrating element. The compositions are thus referred to as
[Gerald Routschka, Pocket manual refractory materials, Vulkan-Verlag 1997, Essen, p. 184]
Refractory compositions are classified according to various criteria, e.g. according to the particle size of the raw materials. Thus, a standard refractory castable has the following composition:
Classification according to raw materials is also customary, typical raw materials are: andalusite, kyanite, mullite, bauxite, flint clays, corundum, magnesia, alumina, dolomite, silicon carbide, zirconia, etc.
Refractory compositions further comprise hydraulic binders such as alumina cements, phosphates and alkali metal silicates (Gerald Routschka, Pocket manual refractory materials, Vulkan-Verlag 1997, Essen, pp. 25–37).
It is known that polyacrylates and polyphosphates can be used as fluidizers for refractory compositions comprising alumina cement, with polyacrylates giving good flowability and a good saving of water (N. Bunt, et al., LAFARGE, UNITECR; Vol, 3, p. 1347, 1997, New Orleans). The use of different types of dispersant enables the water content of free-flowing compositions to be reduced to 5.0–6.0% by weight (based on the total weight of ingredients). This also results in low porosity values and in increased strength values, which in turn leads to a longer life.
Owing to the ever increasing demands made on unshaped refractory products in terms of quality of the compositions and subsequently also their life, there has been no lack of attempts to improve the flow properties or the proportion of water necessary by addition of other organic compounds, e.g. citric acid.
However, it has been found that the proportion of water in such combinations could be decreased only insignificantly, and in many cases the life is still not satisfactory.
More recently developed graft polymers based on polyalkylene oxides as fluidizers for binder suspensions comprising alumina cement (cf. DE 198 08 314 and N. Bunt, et al.; LAFARGE, UNITECR; Vol. 3, p. 1347, 1997, New Orleans) make it possible to produce free-flowing refractory compositions, particularly ones based on alumina, using a minimal amount of make-up water. However, they have the disadvantage that the addition of microsilica, a customary and therefore widespread additive for refractory compositions, reduces their effect or sometimes even makes them completely ineffective.
The hitherto unsatisfactory state of the art therefore leads to the objective of developing fluidizers and/or setting retarders for refractory compositions comprising alumina cement which do not suffer from the reduction in activity on addition of microsilica and which allow, for a minimal amount of make-up water, the production of free-flowing refractory compositions which can be deaerated or densified without use of vibrators.
This object is achieved as set forth herein by the use of water-soluble copolymers which have been prepared from at least two monomers selected from among
In the industrial use of the copolymers, it has, quite surprisingly, been found that the copolymers, whose composition can vary widely, not only have the desired fluidizing properties but also significantly delay the curing of the refractory compositions, which additionally allows significantly longer processing times and was not to be expected.
The component a) is a dicarboxylic acid. Although a dispersant action of copolymers of aliphatic, monoethylenically unsaturated dicarboxylic acids and unsaturated monomers has previously been described, they have been used exclusively as additives for drilling fluids or for reducing deposits (EP-A 398 724).
Among the possible components a) encompassed by the formula I, maleic acid, maleic anhydride, fumaric acid, itaconic acid, itaconic anhydride and/or citraconic acid have been found to be particularly useful for giving the copolymers the desired properties.
Among the many percentage compositions which are likewise possible, preference is given to those which comprise 20–80% of the component a) and/or 10–70% of the component b) and/or 10–70% of the component c).
Copolymers which have been found to be most suitable for fluidizing refractory compositions comprising alumina cement are ones which have a mean molecular weight Mw of <50,000 and preferably of from 1,000 to 15,000. In this context, it is advisable to determine the molar masses by means of GPC. A polyacrylate having a mean molecular weight Mw=4,500 should be used as standard.
The copolymers to be used according to the invention can be prepared in a manner known per se by reacting the monomers at temperatures of from −10 to +100° C., preferably at from 20 to 80° C., in the presence of suitable polymerization catalysts (Polymer Handbook, Third Edition, Brandrup, Immergut, John Wiley and Sons, 1989, p. II/1–II/59). The polymerization is advantageously carried out in the aqueous phase, but, if desired, aqueous solutions of water-miscible solvents such as methanol, ethanol or tert-butyl alcohol can also serve as polymerization medium. As polymerization catalysts, it is possible to use known initiator systems based on organic or inorganic compounds. Preference is given to per compounds such as benzoyl peroxide, acetyl peroxide, tert-butyl hydroperoxide or alkali metal peroxodisulfates and ammonium peroxodisulfate, redox systems or azobisisobutyramidine dihydrochloride. The addition of cocatalysts such as traces of copper, iron or cobalt salts or mercaptans may be advantageous.
Subsequent to the actual polymerization, the carboxyl functions can be converted partly or completely into the salt form by reaction with bases. This reaction can be carried out using the customary basic substances such as alkali metal and alkaline earth metal compounds or ammonia, with the pH preferably being set to from 6.5 to 9.5.
The copolymers are obtained as viscous, preferably aqueous solutions. According to the invention, they can readily be used in this form. If use of the copolymers in solid form is intended, the polymer solutions obtained can be processed further by evaporation or drying processes, e.g. spray drying or drum drying.
The copolymers obtained in this way by known methods are thus, according to the invention, most suitable as fluidizers for refractory compositions comprising alumina cement, e.g. low cement castables (LCCs) or ultra low cement castables (ULCCs), to which they are, according to the invention, added in an amount of from 0.01 to 10% by weight, particularly preferably in an amount from 0.05 to 1.0% by weight. Suitable hydraulic binders are especially alumina cements and suitable ceramic binders are silicate compounds, e.g. microsilica, in an amount of from 0 to 20% by weight and preferably aluminum oxide compounds, e.g. andalusite, bauxite, corrundum, clay and spinels, which are present in an amount of from 1 to 100% by weight, in each case based on the solids content of the refractory composition. For use according to the invention, the copolymers can be used in liquid form or as powders, with the liquid form generally being a solution in water, and the concentration can vary depending on the field of application and the method of use.
For use according to the invention, the copolymers can also be admixed with quality-improving additives in the form of finely divided silica, powdered lime, limestone, soda or potash, which are then present in the copolymers in amounts of from 1 to 30% by weight, based on the dry weight of the polymers.
In a preferred embodiment, the invention further provides for the copolymers to be combined with known, customary fluidizers for refractory compositions and/or with other additives in an amount of from 0.1 to 95% by weight, based on the solids content of the polymers, and, if desired, to be processed further as described above. Typical dispersants or additives of this type are, for example, naphthalenesulfonate-formaldehyde condensation products, sulfonated melamine-formaldehyde condensation products, ketone-formaldehyde-sulfite condensation products, polycarboxylates, lignosulfonates, hydroxycarboxylates, polyphosphates, aromatic sulfonate derivatives, phosphonates, citrates or aromatic hydroxycarboxylic acids or their salts.
Examples of other additives which may likewise be added to the copolymers for the application claimed are air pore formers, accelerators, retarders, antifoams, foaming agents and stabilizers.
The present invention thus serves to influence the flow bahavior of a refractory mixture by using an effective amount of the polymers described or a combination thereof with quality-improving additives, customary fluidizers or other additives for refractory compositions in a ready-to-use mixture. The amount employed naturally depends on the refractory composition itself and is generally selected so that the latter acquires the desired consistency or processibility with an appropriate reduction in the amount of water. As already stated, it was completely unexpectedly found when using the water-soluble copolymers according to the invention that the copolymers can additionally exercise significant retarding influences on the curing behavior of refractory compositions, which makes the polymers used according to the invention simultaneously suitable as setting retarders. Setting retarders are additives which lengthen the time for hydraulic setting of a cement.
In every case, the present invention overcomes the greatest previous disadvantage of strongly water-reducing fluidizers for refractory compositions, as in the case of, for example, the known graft polymers, namely the drop in effectiveness when microsilica is present in the refractor compositions comprising alumina cement.
In particular, the use of a three-component water-soluble polymer comprising 5–90% by weight of a component a), preferably of the maleic acid, fumaric acid or itaconic acid type, 5–90% by weight of a component b) consisting essentially from the group consisting of 2-acrylamido-2-methylpropanesulfonic acid, vinylsulfonic acid and vinylphosphonic acid, and 5–90% by weight of the component c) comprising acrylic acid, methacrylic acid, acrylamide or methacrylamide as fluidizer for refractory compositions comprising alumina cement is described. The copolymer, which has a preferred molecular weight Mw of <50,000, can also be combined with further quality-improving additives such as silica, lime or soda and further customary additives for refractory compositions.
The following examples illustrate the advantages of the present invention.
1) Preparative examples
In a 1 l reaction vessel provided with reflux condenser, stirrer, thermometer, dropping funnel and nitrogen inlet, 98 g of maleic anhydride, 103.5 g of 2-acrylamido-2-methylpropanesulfonic acid and 36 g of acrylic acid were dissolved in 480 g of water under a nitrogen atmosphere. While passing nitrogen into the vessel, the reaction solution was heated to 60° C. in a water bath and 4.3 g of ammonium peroxodisulfate and 8.5 g of 2-mercaptoethanol in 20 g of water were added dropwise. The reaction mixture was stirred under nitrogen for 1.5 hours at 70° C. It was then cooled to room temperature and neutralized to pH 7 using sodium hydroxide. The resulting product was a clear polymer solution having a solids content (SC) of 32% by weight and a molecular weight Mw≈2,500.
43.5 g of acrylic acid, 80 g of maleic anhydride, 20 g of itaconic acid and 103.5 g of 2-acrylamido-2-methylpropanesulfonic acid were reacted by a method analogous to Preparative Example 1. The resulting product was a clear polymer solution having a solids content (SC) of 32% by weight and a molecular weight Mw≈2,000.
103.5 g of 2-acrylamido-2-methylpropanesulfonic acid, 21.6 g of acrylic acid and 56.1 g of itaconic anhydride were reacted in the presence of 2.5 g of ammonium peroxidedisulfate and 5.0 g of 2-mercaptoethanol using a method analogous to Preparative Example 1. The resulting product was a clear polymer solution having a solids content (SC) of 26% by weight and a molecular weight Mw≈3,000.
2) Use example according to the invention
The following examples show the fluidizing action of a commercial polyacrylate fluidizer compared to the fluidizing action according to the invention of the copolymers obtained as described in Preparative Examples 1–3:
The flowability was determined on a refractory concrete having the following composition:
1)The amount of fluidizer and make-up water added in each case reported in % by weight based on the refractory mixture.
The free-flowing refractory composition was prepared and tested in accordance with ENV standard 1402-4. Here, the mixture is placed in a cone having a diameter at the bottom of 10 cm, a diameter at the top of 7 cm and a height of 8 cm and the cone is lifted off in an upward direction. The diameter of the spread-out cake in cm as a function of time indicates the flowability of the refractory composition.
The values obtained in the measurements using the copolymers proposed according to the invention are listed in Table 1. For comparison, the flowability of the refractory composition without addition of fluidizers (C1) and using the commercial fluidizer based on polyacrylate (C2) are shown:
| Number | Date | Country | Kind |
|---|---|---|---|
| 198 30 760 | Jul 1998 | DE | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP99/04813 | 7/8/1999 | WO | 00 | 2/13/2001 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO00/02827 | 1/20/2000 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 4015991 | Persinski et al. | Apr 1977 | A |
| 4331773 | Hongo et al. | May 1982 | A |
| 4334029 | Naito et al. | Jun 1982 | A |
| 4608353 | Nagayama | Aug 1986 | A |
| 4674574 | Savoly et al. | Jun 1987 | A |
| 4888059 | Yamaguchi et al. | Dec 1989 | A |
| 5472051 | Brothers | Dec 1995 | A |
| 5911820 | Satoh et al. | Jun 1999 | A |
| 5912284 | Hirata et al. | Jun 1999 | A |
| Number | Date | Country |
|---|---|---|
| 607039 | Jul 1994 | EP |
| 0 632 186 | Jan 1995 | EP |
| 0 633 390 | Jan 1995 | EP |
| 633390 | Jan 1995 | EP |
| 07291691 | Nov 1995 | JP |
| WO 9528362 | Oct 1995 | WO |
