Patent Application
20090127489
This invention relates to saline soluble, non-metallic, amorphous, inorganic oxide, refractory fibrous materials. The invention particularly relates to glassy fibres having silica as their principal constituent.
Inorganic fibrous materials are well known and widely used for many purposes (e.g. as thermal or acoustic insulation in bulk, mat, or blanket form, as vacuum formed shapes, as vacuum formed boards and papers, and as ropes, yarns or textiles; as a reinforcing fibre for building materials; as a constituent of brake blocks for vehicles). In most of these applications the properties for which inorganic fibrous materials are used require resistance to heat, and often resistance to aggressive chemical environments.
Inorganic fibrous materials can be either glassy or crystalline. Asbestos is an inorganic fibrous material one form of which has been strongly implicated in respiratory disease.
It is still not clear what the causative mechanism is that relates some asbestos with disease but some researchers believe that the mechanism is mechanical and size related. Asbestos of a critical size can pierce cells in the body and so, through long and repeated cell injury, have a bad effect on health. Whether this mechanism is true or not regulatory agencies have indicated a desire to categorise any inorganic fibre product that has a respiratory fraction as hazardous, regardless of whether there is any evidence to support such categorisation. Unfortunately for many of the applications for which inorganic fibres are used, there are no realistic substitutes.
Accordingly there is a demand for inorganic fibres that will pose as little risk as possible (if any) and for which there are objective grounds to believe them safe.
A line of study has proposed that if inorganic fibres were made that were sufficiently soluble in physiological fluids that their residence time in the human body was short; then damage would not occur or at least be minimised. As the risk of asbestos linked disease appears to depend very much on the length of exposure this idea appears reasonable. Asbestos is extremely insoluble.
As intercellular fluid is saline in nature the importance of fibre solubility in saline solution has long been recognised. If fibres are soluble in physiological saline solution then, provided the dissolved components are not toxic, the fibres should be safer than fibres which are not so soluble. The shorter the time a fibre is resident in the body the less damage it can do. H. Förster in ‘The behaviour of mineral fibres in physiological solutions’ (Proceedings of 1982 WHO IARC Conference, Copenhagen, Volume 2, pages 27-55 (1988)) discussed the behaviour of commercially produced mineral fibres in physiological saline solutions. Fibres of widely varying solubility were discussed.
International Patent Application No. WO87/05007 disclosed that fibres comprising magnesia, silica, calcia and less than 10 wt % alumina are soluble in saline solution. The solubilities of the fibres disclosed were in terms of parts per million of silicon (extracted from the silica containing material of the fibre) present in a saline solution after 5 hours of exposure. The highest value revealed in the examples had a silicon level of 67 ppm. In contrast, and adjusted to the same regime of measurement, the highest level disclosed in the Förster paper was equivalent to approximately 1 ppm. Conversely if the highest value revealed in the International Patent Application was converted to the same measurement regime as the Förster paper it would have an extraction rate of 901,500 mg Si/kg fibre—i.e. some 69 times higher than any of the fibres Förster tested, and the fibres that had the highest extraction rate in the Förster test were glass fibres which had high alkali contents and so would have a low melting point. This is convincingly better performance even taking into account factors such as differences in test solutions and duration of experiment.
International Patent Application No. WO89/12032 disclosed additional fibres soluble in saline solution and discusses some of the constituents that may be present in such fibres.
European Patent Application No. 0399320 disclosed glass fibres having a high physiological solubility.
Further patent specifications disclosing selection of fibres for their saline solubility include for example European 0412878 and 0459897, French 2662687 and 2662688, PCT WO86/04807, WO90/02713, WO92/09536, WO93/22251, WO94/15883, WO97/16386 and U.S. Pat. No. 5,250,488.
The refractoriness of the fibres disclosed in these various prior art documents varies considerably and for these alkaline earth silicate materials the properties are critically dependent upon composition.
WO94/15883 disclosed a number of fibres that are usable as refractory insulation at temperatures of up to 1260° C. or more. These fibres comprised CaO, MgO, SiO2, and optionally ZrO2 as principal constituents. Such fibres are frequently known as CMS (calcium magnesium silicate) or CMZS ((calcium magnesium zirconium silicate) fibres. WO94/15883 required that any alumina present only be in small quantities.
A drawback found in use of these fibres, is that at temperatures between about 1300° C. and 1350° C. the fibres undergo a considerable increase in shrinkage. Typically, shrinkages increase from about 1-3% at 1200° C.; to, say, 5% or more at 1300° C.; to >20% at 1350° C. This means that, for example, a temperature overrun on a furnace can result in damage to the insulation and hence to the furnace itself.
A further drawback is that calcium magnesium silicate fibres can react with, and stick to, alumina containing materials due to formation of a eutectic composition. Since aluminosilicate materials are widely used this is a major problem.
WO97/16386 disclosed fibres that are usable as refractory insulation at temperatures of up to 1260° C. or more. These fibres comprised MgO, SiO2, and optionally ZrO2 as principal constituents. As with WO94/15883, this patent required that any alumina present only be in small quantities.
While these fibres do not show the dramatic change in shrinkage evident in the fibres of WO94/15883, they do show a significantly higher shrinkage at normal use temperatures typically having a shrinkage of 3-6% over the range 1200° C.-1450° C. These fibres do not appear to have the drawback of reacting with and sticking to alumina containing materials, however they tend to be difficult to make.
The applicants have invented a group of fibres that have a lower shrinkage across a range of temperatures than the fibres of WO97/16386, while having a higher onset of increase in shrinkage, and a more gentle change in shrinkage, than the fibres of WO94/15883 and which also have a reduced tendency to react with and stick to alumina.
Accordingly, the present invention provides thermal insulation for use in applications requiring continuous resistance to temperatures of 1260° C. without reaction with alumino-silicate firebricks, the insulation comprising fibres having a composition in wt %
65%<SiO2<86%
MgO<10%
14%<CaO<28%
Al2O3<2%
ZrO2<3%
B2O3<5%
P2O5<5%
72%<SiO2+ZrO2+B2O3+5*P2O5
95%<SiO2+CaO+MgO+Al2O3+ZrO2+B2O3+P2O5.
A preferred range of compositions is:—
72%<SiO2<80%
18%<CaO<26%
0%<MgO<3%
0%<Al2O3<1%
0%<ZrO2<1.5%
98.5%<SiO2+CaO+MgO+Al2O3+ZrO2+B2O3+P2O5.
A still more preferred range has the composition:—
72%<SiO2<74%
24%<CaO<26%
Additionally, the applicants have found that addition of small amounts of lanthanide elements, particularly lanthanum, improves the quality of the fibres, particularly their length and thickness, such that improved strength results. There is a trade-off in terms of slightly lower solubility, but the improved strength is of help, particularly in making such products as blankets, in which the fibres are needled to form an interlocking web of fibres.
Accordingly, the present invention comprises a silicate fibre comprising:—
65%<SiO2<86%
MgO<10%
14%<CaO<28%
Al2O3<2%
ZrO2<3%
B2O3<5%
P2O5<5%
72%<SiO2+ZrO2+B2O3+5*P2O5
95%<SiO2+CaO+MgO+Al2O3+ZrO2+B2O3+P2O5.
0.1%<R2O3<4%
where R is selected from the group Sc, La, Ce, Pr, Nd, Sm, Eu, Gd, Th, Dy, Ho, Er, Tm, Yb, Lu, Y or mixtures thereof.
The preferred elements are La and Y. Preferably, to achieve significant improvements in fibre quality, the amount of R2O3 is greater than 0.25%, more preferably >0.5%, and still more preferably >1.0%. To minimise the reduction is solubility that occurs, the amount of R2O3 is preferably <2.5%, still more preferably <1.5% by weight. Very good results are obtained for a fibre having the composition in wt %:—
Further features of the invention will become apparent from the claims in the light of the following illustrative description and with reference to the drawing
The inventors produced a range of calcium silicate fibres using an experimental rig in which a melt was formed of appropriate composition, tapped through a 8-16 mm orifice, and blown to produce fibre in a known manner. (The size of the tap hole was varied to cater for the viscosity of the melt—this is an adjustment that must be determined experimentally according to the apparatus and composition used).
The fibres were tested and the results for fibres that are predominantly calcium silicate fibres with some MgO are shown in Table 1, in which:—
The shrinkage was measured by the method of manufacturing vacuum cast preforms, using 75 g of fibre in 500 cm3 of 0.2% starch solution, into a 120×65 mm tool. Platinum pins (approximately 0.1-0.3 mm diameter) were placed 100×45 mm apart in the 4 corners. The longest lengths (L1 & L2) and the diagonals (L3 & L4) were measured to an accuracy of ±5 m using a travelling microscope. The samples were placed in a furnace and ramped to a temperature 50° C. below the test temperature at 300° C./hour and ramped at 120° C./hour for the last 50° C. to test temperature and left for 24 hours. On removal from the furnace the samples were allowed to cool naturally. The shrinkage values are given as an average of the 4 measurements.
The inventors found that those fibres having a silica content less than 72% by weight tended to stick to the aluminosilicate brick. They also found that high MgO content fibres (>12%) did not stick (as predicted from the properties of WO97/16386).
It is known that calcium silicate fibres having an intermediate level of MgO (12-20%) stick to aluminosilicate brick, whereas magnesium silicate fibres do not. Surprisingly, for the fibres of the present invention, such intermediate levels of MgO can be tolerated. Levels of <10% MgO, or <5% MgO give the non-sticking results required, but it appears preferable for refractoriness to have a maximum level of MgO at 2.5% by weight, and more preferably the amount should be below 1.75% by weight.
Table 2 shows the effect of alumina and zirconia on these fibres. Alumina is known to be detrimental to fibre quality and the first three compositions of Table 2 have over 2% Al2O3 and stick to aluminosilicate brick. Additionally, increased alumina leads to lowered solubility. Accordingly, the inventors have determined 2% as the upper limit for alumina in their inventive compositions.
In contrast zirconia is known to improve refractoriness and Table 2 shows that silica levels of below 72% can be tolerated if the amount of ZrO2 is sufficient that the sum of SiO2 and ZrO2 is greater than 72% by weight. However, increasing zirconia lowers the solubility of the fibres in physiological saline solution and so the preferred level of ZrO2 is less than 3%.
The effect of some other common glass additives is indicated by Table 3, which shows the effect of P2O5 and B2O3 as glass forming additives. It can be seen that P2O5 has a disproportionate effect on the sticking properties of these compositions, as fibres with as low as 67.7% SiO2 do not stick to aluminosilicate brick.
B2O3 also has an effect with fibres having as low as 70.9% SiO2 not sticking. The inventors have determined that sticking to aluminosilicate brick tends not to occur for fibres meeting the relationship:—
72%<SiO2+B2O3+ZrO2+5*P2O5.
The inventors have assumed a maximum level for B2O3 and P2O5 of 5% by weight each.
Tables 1 to 3 show that minor amounts of other components may be included and the invention tolerates up to 5% of other ingredients, but preferably these other ingredients amount to less than 2%, more preferably less than 1%, since such other ingredients tend to make the fibres less refractory. (But see below for effect of specific lanthanide additives).
The above results were obtained on an experimental rig, with all of the uncertainties that entails. Production trials of the most favourable appearing fibres were conducted on two separate sites to allow both blowing and spinning of the compositions to be tried. Table 4 shows a selection of the results obtained (duplicates omitted) and shows that a very usable fibre results. The fibres tested in the production trials had compositions falling in the approximate range
72%<SiO2<80%
18%<CaO<26%
0%<MgO<3%
0%<Al2O3<1%
0%<ZrO2<1.5%
with
98.5%<SiO2+CaO+MgO+Al2O3+ZrO2+B2O3+P2O5.
It can be seen that the compositions with an MgO level of greater than 1.75% tended to have a higher shrinkage at 1350° C. than those with a lower MgO level.
It can be seen that Isofrax® and RCF have a shrinkage that is in the range 3-6% over the range 1200 to 1450° C. SW607 Max™, SW607™, and SW612™ have shrinkages in the range 2-5% at 1200° C. but increase rapidly after 1300° C. The fibres of the present invention have a shrinkage of less than 2% up to 1350° C., drift up to 5-8% at 1400° C. and accelerate thereafter.
The fibres of the present invention therefore have the advantage of a lower shrinkage than magnesium silicate, commercial calcium magnesium silicate, or RCF fibres at 1300° C.; commence their increase in shrinkage at a higher temperature than commercial calcium magnesium silicate fibres; have a shallower rise in shrinkage with temperature than commercial calcium magnesium silicate fibres; and do not stick to aluminosilicate brick in the way commercial calcium magnesium silicate fibres may.
The fibres can be used in thermal insulation and may form either a constituent of the insulation (e.g. with other fibres and/or fillers and/or binders) or may form the whole of the insulation. The fibres may be formed into blanket form insulation.
A problem found with the plain calcium silicate fibres described above was that the fibres tend to be short resulting in a poor quality blanket. A means of producing better fibre for blanket was required and the applicants conducted screening tests to investigate the effect on fibre quality of the addition of other elements as additives to the composition. It was found that lanthanide elements, particularly La and Y improved fibre quality. La was determined to be the most commercially interesting element and so after this initial screening test efforts centred on investigating the effect of La.
La2O3 was used as an additive in amounts of 0-4% to a fibre comprising 73.5% SiO2 and balance CaO and minor impurities to determine the optimum amount. It was determined that addition of La2O3 improved fiberisation while not reducing refractoriness. The fibres did not react with alumina bricks. However, at the highest levels of La2O3 the solubility was reduced significantly. Accordingly a compromise level of 1.3-1.5% La2O3 was used for further tests on the fibre composition.
To check and define the optimum formulation in terms of refractoriness and fiberisation for the lanthanum containing material, a study was performed looking to the increase of silica from 67% to 78% SiO2 in a material containing 1.3% La2O3 (kept constant), balance CaO+minor impurities MgO and Al2O3.
Increasing silica increases the refractoriness of the fibre, giving lower shrinkage, higher melting point and decreases reaction with alumina at high temperature.
The best compromise between refractoriness and fiberisation was found for a composition of:
This composition was tried on production scale manufacturing blanket having the composition “With La” shown in Table 4 below.
It was confirmed that this composition produced better fibres than an La free version (“No La” in Table 4). The fibres still not reacting with alumina brick, and having good refractoriness.
Better fiberisation was observed and evaluated by looking to the tensile strength of 25 mm thick blanket having a density 128 kg/m3.
It can be seen that the addition of only 1.3% La2O3 results in a considerable improvement in tensile strength, indicating a much improved fibre.
The applicants surmise that this effect of improving fiberisation is a viscosity or surface tension modifying effect applicable generally to alkaline earth silicate fibres, and so the invention encompasses the use of such additives generally in the amounts indicated above to improve fiberisation of alkaline earth silicate fibres.
| Number | Date | Country | Kind |
|---|---|---|---|
| 0200162.6 | Jan 2002 | GB | national |
This patent application is a continuation application based on and claiming priority on U.S. patent application Ser. No. 10/493,340 filed on Apr. 22, 2004, which is the U.S. national phase of International Application No. PCT/GB03/0003 filed on Jan. 2, 2003 and published in English as International Publication No. WO 2003/059835 A1 on Jul. 24, 2003, which application claims priority to Great Britain Application No. 0200162.6 filed on Jan. 4, 2002, now British Patent 238793, the contents of which are incorporated by reference therein.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10493340 | Apr 2004 | US |
| Child | 12275035 | US |
