GB2337993A - Alkaline earth silicate mastics - Google Patents
Alkaline earth silicate mastics Download PDFInfo
- Publication number
- GB2337993A GB2337993A GB9820123A GB9820123A GB2337993A GB 2337993 A GB2337993 A GB 2337993A GB 9820123 A GB9820123 A GB 9820123A GB 9820123 A GB9820123 A GB 9820123A GB 2337993 A GB2337993 A GB 2337993A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mastic
- fibres
- colloidal silica
- alkaline earth
- fibre
- 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.)
- Granted
Links
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/16—Making or repairing linings increasing the durability of linings or breaking away linings
-
- 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
-
- 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
- C04B30/00—Compositions for artificial stone, not containing binders
- C04B30/02—Compositions for artificial stone, not containing binders containing fibrous materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/34—Filling pastes
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1025—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by non-chemical features of one or more of its constituents
- C09K3/1028—Fibres
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F27—FURNACES; KILNS; OVENS; RETORTS
- F27D—DETAILS OR ACCESSORIES OF FURNACES, KILNS, OVENS, OR RETORTS, IN SO FAR AS THEY ARE OF KINDS OCCURRING IN MORE THAN ONE KIND OF FURNACE
- F27D1/00—Casings; Linings; Walls; Roofs
- F27D1/0003—Linings or walls
- F27D1/0006—Linings or walls formed from bricks or layers with a particular composition or specific characteristics
- F27D1/0009—Comprising ceramic fibre elements
-
- 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
- C04B2111/00663—Uses not provided for elsewhere in C04B2111/00 as filling material for cavities or the like
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Structural Engineering (AREA)
- Inorganic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Nonwoven Fabrics (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Sealing Material Composition (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Ceramic Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Furnace Housings, Linings, Walls, And Ceilings (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
Mastics are provided in which separately or in combination the mastic comprises:- 1) a) alkaline earth metal silicate refractory fibres; and, b) colloidal silica having a pH of below 8. 2) a) alkaline earth metal silicate fibres; and b) a non-ionic polymer viscosity modifier. 3) a) alkaline earth metal silicate fibres; and b) a multi-dentate calcium-complexing ligand.
Description
-2337993 REFRACTORY MASTICS This invention relates to refractory mastics
and is particularly applicable to mastics comprising saline soluble fibres bonded with a binder comprising colloidal silica.
Refractory ceramic fibres (RCF) are well known materials and typically comprise an aluminosilicate inorganic fibre formed from an oxide melt which is spun, blown, drawn, or otherwise formed into fibres. Such RCF fibres are used in the manufacture of various industrial and domestic articles. Typical uses of RCF are for applications in which resistance to temperatures in excess of io 800'C is required.
Much RCF fibre is used in the form of needled blankets of fibre in which structural integrity is provided by the fibres that are tangled together in the needling process. (Such products are known as "blanket"). Sometimes a binder is used to lock the fibres together subsequent to exposure to high temperature. Blanket can be processed further to form cut shapes or folded to form insulating modules.
RCF fibre is also used in the production of so-called "Converted Products". Converted products comprise materials in which the RCF is processed further to provide materials in which the RCF is present as either a minor or major constituent. Typical converted products include the following:"Board" - "Shapes" - "Fire shapes"- substantially rigid flat sheets containing inorganic and/or organic binders produced by a wet process (for example made by dehydrating a suspension of RCF and binders); a flexible fibrous insulating material with a thickness of less than or equal to 6mm, formed on paper making machinery (for example RCF in sheet form with a binder); substantially rigid shapes made of ceramic fibre with the addition of inorganic and/or organic binder, fired or unfired (for example,RCF formed by vacuum forming into a variety of shapes); RCF formed by a vacuum forming route and used for domestic and industrial fires either as radiant bodies or for decorative appearance; "Castables"ceramic fibre with inorganic andlor organic binder which may be cast (for example, RCF in the form of cements, concretes and mortars); 1 "Mastics" A mouldable material containing RC17 with binders and which may be trowelled, hand moulded, or dispensed from a pressure gun and which sets upon drying/heating; "Extrusion" - A mastic-like material that may be used in the manufacture of extruded sections and tubes.
"Textiles" - ceramic fibre which has been woven with or without the addition of other filaments, wires, or yarns (for example, RCF formed into rope, yarn, mats and the like by textile technology).
io In many of the above mentioned applications binders are used. There are two broad classes of binders:- "Organic binders" - which serve to improve the handling characteristics of the product concerned at low temperatures but which bum off at higher temperatures. Organic binders include, for example, such materials as starch.
1norganic binders" - which may be effective to Improve the handling characteristics of the product concerned at low temperatures, but which also give integrity to the product after exposure to high temperatures. Inorganic binders include, for example, such materials as colloidal silicas, aluminas, and clays.
All of the above materials and concepts are well known in the reftactory industry.
Although extremely useful, RC17 is an inorganic fibrous material. 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 ftaction 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.
2 Accordingly there is an industry and regulatory demand for inorganic fibres that Vaill 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 that are not so soluble. Accordingly, in recent years, a number of different types of fibre have been proposed which are refractory and yet soluble in body fluids. Such fibres comprise alkaline earth silicates (e. g. W087/05007, W089/12032, W093/15028, W094/15883, W096/02478, and W097/49643) which are soluble to varying extent in body fluids.
A problem with saline soluble fibres is that by their nature they are more reactive than RC17 and therefore cannot always be used as a direct replacement for RCE Mastics are required to have a reasonable shelf life, which for RC17 containing mastics is generally about 6 months. Mastics made using alkaline earth metal silicates have had such a short shelf life as to be unusable. The applicants have realised that this is due to the reactivity of the fibres with the binders. Calcium ions released from the alkaline earth metal silicate fibres set the organic and inorganic constituents of the mastic.
The present invention provides a mastic comprising:- a) b) inorganic refractory fibres- and, colloidal silica characterised in that the inorganic refractory fibres are alkaline earth metal silicates and the colloidal silica has a pH of below 8. Preferably the pH is below 7 and may usefully lie in the range 4 to 7.
Further features of the invention are made apparent in the attached claims and the following description with reference to the drawings in which-
3 Fig. 1 is a schematic view of a penetrometer used in measuring the characteristics of mastics; Figs. 2 to 5 are graphs showing penetrometer readings for various mastic compositions.
The invention is exemplified in the following with reference to the alkaline earth silicate fibres SUPERWOOL 607m and SUPERWOOL 612'rm (both available from Thermal Ceramics Limited of Bromborough, England).
SUPERWOOL 607m has a nominal composition (by weight) Of Si02 65%, CaO 29. 5%, MgO 5.5%, and A1203 <1% and is usable at temperatures up to 1050T.
SUPERWOOL 612'rm has a nominal composition (by weight) of S102,64%, CaO 17%, MgO 13.5%, Zr02 5%, impurities 0.5% and is usable at temperatures up to 1260T.
Fibre mastics or mouldables are used to repair fibre linings of kilns. SUPERWOOL 612'rm has been used to replace refractory ceramic fibre in many applications but when used in current mastic formulations as a replacement for RCF the shelf life is not satisfactory and certainly will not be useable 6 months after manufacture. The applicants have shown that by using certain types of colloidal silica andlor a different viscosity modifier and/or calcium scavenging multi-dentate I lgands then the shelf life can be much extended over the standard formulation.
The fibres used in experiments of mastic compositions were SUPERWOOL 612'rm and SUPERWOOL 607m. The latter fibre was used in an attempt to predict the long-term effects on the SUPERWOOL 612'rm fibre. Typically a standard mastic mix with SUPERWOOL 612Tm as a one for one replacement of RCF will be useable up to about three weeks compared to only 1-2 days with the SUPERWOOL 607m fibre which is much more reactive. A standard RCF fibre (HY20TM(46%A1203/54%SiO2)obtainable flom Thermal Ceramics Limited, Bromborough, England) was used as a comparison.
4 The standard procedure for producing a mastic in these experiments was to first combine the ingredients of colloidal silica, water, biocide and dye (if appropriate) with a paddle-type stirrer. Then the viscosity modifier was slowly added to this liquid which was allowed to thicken on standing (3 - 5 minutes). A Hobart-type mixer was used to break down the bulk fibre for 10- 15 seconds on low speed before the thickened liquor was added. After about 1 niinute the speed was then increased to its maximum for 4 minutes to obtain a homogenous mixture that had a consistency that was stiff/creamy. The mastic would then be ready for use or for storage in airtl(xht containers.
C Measurement of the stability of the formulations tested was made with the use of a penetrometer (Fig. 1). The penetrometer had two rams 1 (one aluminium and the other steel of respective masses 109 g and 3 3 6g) which gave the ability to measure quite different consistencies due to the different weights involved. The lever 2 on top of the penetrometer was used to release the ram to drop down and penetrate the mastic. Indicator mark 3 was viewed through window 4 and compared with scale 5 (in mm). Higher penetration readings represented mastic of lower viscosity.
The procedure involved stirring the mastic thoroughly in the container before attempting to take any reading. Then the penetrometer (with the aluminium ram) was placed on top of the mixture before pressing the lever 2. This reading was then recorded before repeating in a different area until 5 readings were obtained. The process was then repeated using the steel ram. Usually the mastic (-2.5kg) was split into three containers and each of these measured in the same way. Readings were then averaged and the result plotted against age of the mastic. Tables 1 and 2 below indicate the mastic formulations used (amounts in weight %) and Table 3 indicates the nature of the colloidal silicas and viscosity modifiers used.
RCF 612 612 612 612 612 612 612 612 Standard STD TMA LS SK & M Magnafloc Magnafloc 11 TCL SK EDTA % % % % % % % % % Colloidal Nyacol 1430 47.9 48.0 48.3 48.3 48.0 Silica Ludox TMA 42.3 Ludox LS 48.0 Ludox SK 57.7 57.5 Water Water (pH 6.5) 19.6 19.8 25.4 19.8 10.1 19.5 19,5 10.1 19.8 Biocide Slimicide C 508 E 0.01 0,01 0.01 0,01 0.01 0.01 0.01 0.01 0,01 Dye HD Kenalake 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 drops Orange 2R Anti-freeze Ethylene glycol Viscosity Magnafloc 139 2.0 2.2 2.2 2.2 2.2 2.2 Modifier Magnafloc 351 1.9 1.9 1.7 EDTA 0.4 Fibre HY20 30.5 612 30.1 30.1 30.1 30.2 30.3 30.3 30.1 30.1 % Si02 in mix 14.4 14.4 14.4 14.4 14.4 14.5 14.5 14.4 14.3 Table 1 Formulations using SUPERWOOL 612TMfibre 6 607 607 607 607 607 607 607 607 RCF 607SK 607 Standard Magna T STD& SK& SK EDTA EDTA Detrick Detric Detrick m m m HPMC (2) k Colloidal Nyacol 1430 48.0 48,0 48.0 48.0 48.0 64.2 64.1 Silica Ludox TMA 42.4 Ludox SK 52.1 52.1 71.1 Water Water (pH 6.5) 19.4 19.4 25.5 19.35 10.1 10.1 19.4 19.8 Biocide Slimicide C 0.01 0.01 0.01 0.01 0.01 0 0.01 0 0.05 0.10 508 E Dye HD Kenalake 1-2 drops 1-2 drops 1-2 drops 1-2 drops 1-2 1-2 drops 1-2 1-2 1-2 1-2 drops OranRe 2R drops drops drops drops Anti-freeze Ethylene 6.8 7.6 6.8 gly 01 Viscosity Magnafloc 139 2.2 2.2 2.2 1.7 1.6 Modifier Majznafloc 351 1.9 1.9 1.3 1.9 1.7 I-Ipmc EDTA 0.4 0.4 Fibre HY20 27.2 607 30.1 30.1 30.2 30.1 30.2 30.2 30.1 30.1 30.2 27.2 % Si02 in mix 14.4 14.5 14.4 14.6 14.4 14.4 14.4 14.3 19.3 16.1 19.3 Table 2 - Formulations using 607 fibre Hydroxypropylinethylcellulose (MethocellTm F4M) 7 Colloidal Silicas Ludox TMA Nyacol LS SK 1430 Stabilising Counter ion Sodium Sodium Deionized Deionized Particle Charge Negative Negative Negative Negative Av. particle diameter (rim) 14 12 12 22 Specific surface area, M2/g 220 215 230 140 Silica (as SiO2), wt % 30 30 25 34 pH (25' 10,2 8.2 4-7 4-7 ISupplier -UOt Chemicals Wilmington DE. USA Viscosity Modifiers# Magnafloc (Acrylamide based polymers) 139 351 Active content 90% 90% Particle Charge Anionic Non-ionic pH (25T) 4.5 4.5 Viscosity (1%) 500 900 Molecular wt 7.5 xIO' 13 x 106 previously known as Versicol WN23 #Supplier Allied Colloids Ltd P.O. Box 38 Bradford, West Yorkshire BD12 OJZ, England Table 3. Colloidal Silicas and Viscosity Modifiers 8 The penetrometer tests show that the stability of the SUPERWOOL 612T?4 mastic, as measured using the steel ram, can be extended from approximately 20 days to over 120 days. This was achieved by substituting the standard colloidal silica used in such mastics (NyacoIT"m 1430 - a colloidal silica with a pH of 10.2) by an acidic colloidal silica (LudokTm TMA - a colloidal silica with a pH of 4-7), a different viscosity modifier (Magnafloc 3 5 1), or a combination of both (Ludox SKTm - a colloidal silica with a pH of 4-7 & Magnafloc 3 5 1). The results of the tests are shown in Figures 4 & 5.
Although the values obtained for the alkaline earth metal silicate fibres were not as consistent as those for the RCF fibre the overall trend could easily be seen. Variations may have been due to temperature fluctuations and indeed if curves are plotted on a date basis the variations are in conjunction with each other. The sequence in which the Magnafloc 351 is added also affected the mastic properties. The SUPERWOOL 612Tm Magnafloc H formulation had the viscosity modifier dissolved in water before adding the other ingredients as opposed to the usual method of adding it to the colloidal silica. The Magnafloc, II formulation decreased in viscosity within 1-2 days whereas the Magnafloc mixture took over 20 days before its viscosity also dropped.
An alternative alkaline silica (Ludox LS) produced very similar results to the standard formulation confirming that alkaline solutions are detrimental to the performance of the mastic.
Formulations using SUPERWOOL 607m fibre (Figures 2 & 3) were used as accelerated tests of the SUPERWOOL 612Tm fibre. Values for the standard formulation (using Nyacol colloidal silica) had bottomed out after only 12 days. The Ludox TMA gave about 14 days before it plummeted within a day to its lowest level. This mastic gave very high readings to start with and could not be measured with the steel ram until day 10. The Ludox SKTm with Magnafloc 351 produced fairly linear values at least up to 50 days; if this difference were to be reproduced with the SUPERWOOL 611rm fibre then a shelf life of at least 6 months could be expected.
Magnafloc 3 51 substituted in the standard SUPERWOOL 607m mix alone did not make such a large difference, reaching the same value in 2 days as the standard and then continued to drop below this.
9 An alternative standard formulation for a pumpable mastic containing ethylene glycol (Detrick) was made with SUPERWOOL 607m fibre and this set in less than 1 day. When this formulation was repeated but using LUDOX SICTm colloidal silica the mastic was almost unchanged after 18 days.
As an alternative to the acidic colloidal silicas or the Magnafloc 3 5 1, EDTA has also proven to be reasonably effective extending the normal life of the standard mix by adding only 0.4% EDTA. The mix thickened very quickly over the first few hours but then remained stable. Extra initial water may achieve the required viscosity without altering other properties.
The applicants surmise that provision of an acidic colloidal silica reduces liberation of calcium ions from the fibre; use of the non-Ionic viscosity modifier reduces the risk of setting reactions with the calcium ions released., and provision of multi-dentate ligands such as ethylene glycol and EDTA scavenges and locks up the calcium produced by the fibres. The present invention is not limited to the particular viscosity modifiers and multi-dentate ligands disclosed however.
Claims (10)
- A mastic comprising:a) inorganic refractory fibres. and, b) colloidal silica characterised in that the inorganic refractory fibres are alkaline earth metal silicates and the colloidal silica has a pH of below 8.io
- 2.
- 3.
- 4.
- 5.
- 6.
- 7.A mastic as claimed in claim 1 in which the colloidal silica has a pH of below 7.A mastic as claimed in claim 2 in which the colloidal silica has a pH in the range 4 to 7.A mastic as claimed in any preceding claim in which the colloidal silica is a negatively charged de-ionised sol.A mastic comprising alkaline earth metal silicate fibres and a non-ionic polymer viscosity modifier.A mastic as claimed in claim 5 also comprising colloidal silica as specified in claims 1-4.A mastic comprising alkaline earth metal silicate fibres and a multidentate calciumcomplexing ligand.
- 8.A mastic as claimed in claim 7 in which the multi-dentate calciumcomplexing ligand is, or is derived from, ethylene glycol.
- 9. A mastic as claimed in claim 7 in which the multi-dentate calciumcomplexing ligand is or is derived from ethylenediaminetetraacetic acid (EDTA).
- 10. A mastic as claimed in any of claims 1 to 6 and also comprising a multi-dentate calcium-complexing ligand as claimed in any of claims 7 to 9.11
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9820123A GB2337993B (en) | 1998-09-15 | 1998-09-15 | Refractory mastics |
AU58759/99A AU5875999A (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
EP99946345A EP1115672A1 (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
BR9912238-3A BR9912238A (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
CN99810824A CN1316981A (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
MXPA01002622A MXPA01002622A (en) | 1998-09-15 | 1999-09-14 | Refractory mastics. |
CA002336974A CA2336974A1 (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
KR1020017003334A KR20010079828A (en) | 1998-09-15 | 1999-09-14 | Refractory Mastics |
CZ2001948A CZ2001948A3 (en) | 1998-09-15 | 1999-09-14 | Alkaline earth silicate mastics |
IDW20010606A ID27836A (en) | 1998-09-15 | 1999-09-14 | MASTICS ARE HEAT RESISTANT |
JP2000570118A JP4319355B2 (en) | 1998-09-15 | 1999-09-14 | Fireproof plaster |
PL99346610A PL346610A1 (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
PCT/GB1999/003062 WO2000015573A1 (en) | 1998-09-15 | 1999-09-14 | Refractory mastics |
HK00103049A HK1024226A1 (en) | 1998-09-15 | 2000-05-22 | Refractory mastics |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9820123A GB2337993B (en) | 1998-09-15 | 1998-09-15 | Refractory mastics |
Publications (3)
Publication Number | Publication Date |
---|---|
GB9820123D0 GB9820123D0 (en) | 1998-11-11 |
GB2337993A true GB2337993A (en) | 1999-12-08 |
GB2337993B GB2337993B (en) | 2000-04-12 |
Family
ID=10838919
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9820123A Expired - Fee Related GB2337993B (en) | 1998-09-15 | 1998-09-15 | Refractory mastics |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP1115672A1 (en) |
JP (1) | JP4319355B2 (en) |
KR (1) | KR20010079828A (en) |
CN (1) | CN1316981A (en) |
AU (1) | AU5875999A (en) |
BR (1) | BR9912238A (en) |
CA (1) | CA2336974A1 (en) |
CZ (1) | CZ2001948A3 (en) |
GB (1) | GB2337993B (en) |
HK (1) | HK1024226A1 (en) |
ID (1) | ID27836A (en) |
MX (1) | MXPA01002622A (en) |
PL (1) | PL346610A1 (en) |
WO (1) | WO2000015573A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2786976A4 (en) * | 2011-12-01 | 2014-12-10 | Nichias Corp | Monolithic composition |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BRPI0712442A8 (en) | 2006-05-31 | 2017-10-24 | Unifrax I Llc | SPARE THERMAL INSULATION PLATE |
AU2007327075B8 (en) | 2006-11-28 | 2012-09-06 | Morgan Advanced Materials Plc | Inorganic fibre compositions |
US8627853B1 (en) | 2007-08-17 | 2014-01-14 | Unifrax I Llc | Insulating material for automotive exhaust line tubing and manifolds |
JP4902797B1 (en) | 2011-03-30 | 2012-03-21 | ニチアス株式会社 | Wet blanket |
JP4937414B1 (en) | 2011-03-30 | 2012-05-23 | ニチアス株式会社 | Cured shaped product |
CN105928629A (en) * | 2016-04-29 | 2016-09-07 | 武汉理工大学 | Steel smelting temperature measurement paper clay head and fire-resistant adhesive applied thereto |
KR102393132B1 (en) | 2016-06-06 | 2022-04-29 | 유니프랙스 아이 엘엘씨 | Fire-resistance coating material containing low bio-persistence fibers and method for preparing same |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1204472A (en) * | 1966-08-09 | 1970-09-09 | Foseco Trading Ag | Heat-insulating shaped compositions |
US3835054A (en) * | 1972-07-10 | 1974-09-10 | Nalco Chemical Co | Method for preparation of thermal insulation board |
US4040847A (en) * | 1976-04-14 | 1977-08-09 | Johns-Manville Corporation | Temperature stable fibrous insulation composition and "wet" package formed thereof |
JPS55160081A (en) * | 1980-05-12 | 1980-12-12 | Kyokado Eng Co Ltd | Coagulation of ground |
US4430369A (en) * | 1982-06-01 | 1984-02-07 | Nalco Chemical Company | Silica sol penetration and saturation of thermal insulation fibers |
DE3225161C2 (en) * | 1982-07-06 | 1984-07-12 | Didier-Werke Ag, 6200 Wiesbaden | Process for the production of paste-like fiber masses and their use |
WO1994015883A1 (en) * | 1993-01-15 | 1994-07-21 | The Morgan Crucible Company Plc | Saline soluble inorganic fibres |
EP0710628B1 (en) * | 1993-01-15 | 2003-06-25 | The Morgan Crucible Company Plc | Saline soluble inorganic fibres |
JPH07196350A (en) * | 1993-12-28 | 1995-08-01 | Kyokado Eng Co Ltd | Hardened cement, protecting agent applied thereto and method for protecting hardened cement |
US5658836A (en) * | 1995-12-04 | 1997-08-19 | Owens-Corning Fiberglas Technology, Inc. | Mineral fibers and their compositions |
-
1998
- 1998-09-15 GB GB9820123A patent/GB2337993B/en not_active Expired - Fee Related
-
1999
- 1999-09-14 MX MXPA01002622A patent/MXPA01002622A/en not_active Application Discontinuation
- 1999-09-14 ID IDW20010606A patent/ID27836A/en unknown
- 1999-09-14 EP EP99946345A patent/EP1115672A1/en not_active Withdrawn
- 1999-09-14 CZ CZ2001948A patent/CZ2001948A3/en unknown
- 1999-09-14 AU AU58759/99A patent/AU5875999A/en not_active Abandoned
- 1999-09-14 BR BR9912238-3A patent/BR9912238A/en not_active Application Discontinuation
- 1999-09-14 WO PCT/GB1999/003062 patent/WO2000015573A1/en not_active Application Discontinuation
- 1999-09-14 JP JP2000570118A patent/JP4319355B2/en not_active Expired - Fee Related
- 1999-09-14 CN CN99810824A patent/CN1316981A/en active Pending
- 1999-09-14 PL PL99346610A patent/PL346610A1/en unknown
- 1999-09-14 CA CA002336974A patent/CA2336974A1/en not_active Abandoned
- 1999-09-14 KR KR1020017003334A patent/KR20010079828A/en not_active Application Discontinuation
-
2000
- 2000-05-22 HK HK00103049A patent/HK1024226A1/en not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2786976A4 (en) * | 2011-12-01 | 2014-12-10 | Nichias Corp | Monolithic composition |
Also Published As
Publication number | Publication date |
---|---|
ID27836A (en) | 2001-04-26 |
PL346610A1 (en) | 2002-02-25 |
WO2000015573A1 (en) | 2000-03-23 |
AU5875999A (en) | 2000-04-03 |
GB2337993B (en) | 2000-04-12 |
EP1115672A1 (en) | 2001-07-18 |
CA2336974A1 (en) | 2000-03-23 |
MXPA01002622A (en) | 2002-04-08 |
GB9820123D0 (en) | 1998-11-11 |
CZ2001948A3 (en) | 2001-11-14 |
BR9912238A (en) | 2001-04-10 |
JP4319355B2 (en) | 2009-08-26 |
KR20010079828A (en) | 2001-08-22 |
HK1024226A1 (en) | 2000-10-05 |
JP2002524384A (en) | 2002-08-06 |
CN1316981A (en) | 2001-10-10 |
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Legal Events
Date | Code | Title | Description |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20170915 |