EP1115674A1 - Production de produits d'isolation thermique en matiere de fibres vitreuses - Google Patents

Production de produits d'isolation thermique en matiere de fibres vitreuses

Info

Publication number
EP1115674A1
EP1115674A1 EP99948857A EP99948857A EP1115674A1 EP 1115674 A1 EP1115674 A1 EP 1115674A1 EP 99948857 A EP99948857 A EP 99948857A EP 99948857 A EP99948857 A EP 99948857A EP 1115674 A1 EP1115674 A1 EP 1115674A1
Authority
EP
European Patent Office
Prior art keywords
additive
product
binder
batt
dispersion
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.)
Withdrawn
Application number
EP99948857A
Other languages
German (de)
English (en)
Inventor
Susanne Dyrboel
Erling Lennart Hansen
Trine Frickman
Ian Cridland
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rockwool AS
Original Assignee
Rockwool International AS
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=27443732&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP1115674(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from EP98307761A external-priority patent/EP0989103A1/fr
Priority claimed from GBGB9916175.4A external-priority patent/GB9916175D0/en
Priority claimed from GBGB9916174.7A external-priority patent/GB9916174D0/en
Priority claimed from GBGB9916176.2A external-priority patent/GB9916176D0/en
Application filed by Rockwool International AS filed Critical Rockwool International AS
Priority to EP99948857A priority Critical patent/EP1115674A1/fr
Publication of EP1115674A1 publication Critical patent/EP1115674A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/732—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by fluid current, e.g. air-lay
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/42—Coatings containing inorganic materials
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/42—Coatings containing inorganic materials
    • C03C25/44—Carbon, e.g. graphite
    • C—CHEMISTRY; METALLURGY
    • C03—GLASS; MINERAL OR SLAG WOOL
    • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
    • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
    • C03C25/10—Coating
    • C03C25/465—Coatings containing composite materials
    • C03C25/47—Coatings containing composite materials containing particles, fibres or flakes, e.g. in a continuous phase
    • 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
    • C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02—Granular materials, e.g. microballoons
    • 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
    • C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02—Granular materials, e.g. microballoons
    • C04B14/022—Carbon
    • C04B14/024—Graphite
    • 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
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/413—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties containing granules other than absorbent substances
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4209—Inorganic fibres
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4209—Inorganic fibres
    • D04H1/4218—Glass fibres
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/587—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/60—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in dry state, e.g. thermo-activatable agents in solid or molten state, and heat being applied subsequently
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/736—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged characterised by the apparatus for arranging fibres
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0063—Inorganic compounding ingredients, e.g. metals, carbon fibres, Na2CO3, metal layers; Post-treatment with inorganic compounds
    • E—FIXED CONSTRUCTIONS
    • E04—BUILDING
    • E04B—GENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
    • E04B1/00—Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
    • E04B1/62—Insulation or other protection; Elements or use of specified material therefor
    • E04B1/74—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
    • E04B1/76—Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls specifically with respect to heat only
    • E04B1/78—Heat insulating elements

Definitions

  • This invention relates to thermal insulation products based on man-made vitreous fibres (MMVF) and which are modified in a simple manner so as to give improved thermal insulation as indicated by a reduced ⁇ value.
  • MMVF man-made vitreous fibres
  • MMVF products are known for use in various environments for thermal insulation purposes. It is desirable to try to obtain the best thermal insulation properties available. Various methods for doing this have been suggested in the past.
  • US 3,014,872 describes one method of improving fibre glass or mineral wool. This is done by blowing into the loosely matted product a powdered substance such as silicon, germanium, carbon black or fibrous potassium titanate. It is said to be essential that the powdered material is present in an amount of from 20 to 50% by weight of the fibrous material and 25 wt.% silicon is exemplified. It is stated to be important that the particles have poor thermal contact with the fibres, since good thermal contact would increase thermal losses due to conduction, and that the silicon should adhere lightly to the fibres by electrostatic attraction. The product is used for insulation surrounding an oven in an improved electric range.
  • a powdered substance such as silicon, germanium, carbon black or fibrous potassium titanate. It is said to be essential that the powdered material is present in an amount of from 20 to 50% by weight of the fibrous material and 25 wt.% silicon is exemplified. It is stated to be important that the particles have poor thermal contact with the fibres, since good thermal contact would increase thermal losses due to
  • WO92/09538 refers to US 4,101,335, which it states discloses a "fire resistant asbestos-free building board" comprising mica or a mixture of mica and standard vermiculite distributed in a calcium silicate binder.
  • US 4,919,995 describes the use of gold-coated mica flakes having thickness approximately 1 micron and area a few hundredths of a square millimeter which are distributed throughout a heat insulating device formed from quartz wool or mineral wool. It appears that the flakes must be arranged in a defined pattern (juxtaposed and overlapping) and are oriented so that they are perpendicular to the expected direction of travel of heat. Proportions of these flakes in the product are not specified.
  • EP-B- 500,900 A different type of product is described in EP-B- 500,900. This is produced by producing glass wool panels and subjecting them to vacuum whilst encapsulating them. A particulate material in included which must have a surface area at least 50 m 2 /g (by BET) . Fumed and precipitated silica are exemplified and preferred, although other silicas and graphite are mentioned in the description. The very fine particles are important in the context of this type of vacuum produced product. The product must be free of binder, especially organic binder. US 3,793,204 is also in a different area and does not concern low density, air-laid products. Instead it concerns the production of a molded composite of high density, also for insulation purposes.
  • a thermal insulation product comprising air-laid MMVF material throughout which a particulate additive is distributed substantially homogeneously, characterised in that the additive is selected from the group consisting of silicon, aluminium, mica, silica, titania and mixtures thereof and the particulate additive is held in the MMVF material by being bonded to the surfaces of the MMV fibres by a binder.
  • the construction of the invention allows excellent reduction in ⁇ value at very low levels of particulate additive, in particular lower levels than those described in the prior art.
  • silicon, aluminium and mica, especially silicon and aluminium, and in particular aluminium are especially beneficial.
  • aluminium when aluminium is used it can be used as powder or flakes, preferably flakes.
  • the particulate additive is bonded into the MMVF product with a binder.
  • the MMVF product may be a bonded product, in which case part or all of the binder for the product can conveniently also serve as binder for the additive.
  • a separate binder for the additive may be provided.
  • the product may be a granulate, but a preferred thermal insulation product according to the invention comprises a layer which is an air-laid MMVF batt or batt stratum through which the particulate additive is distributed substantially homogeneously.
  • the product may comprise only MMVF which contains the additive or may have MMVF regions without it (eg in the case of a batt having an additive-containing layer) .
  • the MMVF part of the product consists essentially of MMVF having homogeneously distributed additive.
  • This product may comprise a batt having the additive distributed substantially homogeneously throughout most or all of the batt, in which event the defined layer substantially has the thickness of the batt.
  • the products of the invention include those in which the layer is a stratum of the batt, that is to say that it is a layer within a batt.
  • the batt stratum that is to say the layer which contains the particulate additive, may be from 10 to 80%, often 10 to 20% or 50%, of the thickness of the entire batt.
  • Batts of the invention may comprise more than one layer in which the particulate additive is homogeneously distributed.
  • the layers are disposed perpendicular to the expected direction of heat transfer.
  • the particulate additive can be distributed uniformly throughout the layer or there may be a concentration gradient.
  • the additive is distributed substantially homogeneously in the sense that it should be sufficiently uniformly distributed throughout the volume of the product to minimise the risk of significant amounts of radiation being able to pass through the level without encountering the additive. Accordingly the areas of the layer which are substantially free of additive should be as low as possible.
  • ⁇ value of a batt by at least 0.5 units (e.g. from 35.5 mW/mK down to 35.0) and generally by at least 0.8 or 1 unit (e.g. 1 to 3 units or more) .
  • air-laid MMVF insulation products generally show a decrease in ⁇ as density increases (to an eventual minimum at very high density) .
  • a lower thickness can be used to give equivalent insulation value.
  • the ability to provide lower density also gives transportation and storage advantages.
  • Lower density products have greater compressibility. However, they also retain good recovery. Therefore a lower density product can be compressed to reduce its volume for transportation and then recover substantially all its original thickness for use (in particular to the thickness of an equivalent product without additives) .
  • the invention allows the achievement of lower density (and hence higher compressibility) at equivalent or even better ⁇ value.
  • a product according to the invention and containing aluminium can be provided at a density of 29 kg/m 3 with ⁇ 10 of 35 mW/mK, in contrast to a product not containing any aluminium which has density of 34 kg/m 3 but the same ⁇ value.
  • the compressibility of the 34 kg/m 3 product is 22% whereas the compressibility of the 29 kg/m 3 product is 30%. Thus the 29 kg/m 3 product may be transported more efficiently and does not have impaired recovery.
  • preferred products of the invention are products which have been compressed by at least 25%, preferably at least 30%.
  • the density before compression is preferably not more than 30 kg/m 3 .
  • the product is preferably releasably compressed, ie when the compression force is removed it recovers substantially all of its pre-compression thickness (for instance at least 70% of its pre-compression thickness) .
  • Such compressed products are often usefully produced for transportation and storage purposes.
  • the invention also includes the production of a product of the invention, especially a batt product, having density of not more than 30 kg/m 1 and compression of that product by at least 25%, preferably at least 30%.
  • the ⁇ 10 of the pre-compressed product is preferably not more than 45 mW/mK, more preferably not more than 40 mW/mK, or even more preferably not more than 37 mW/mK.
  • the amount of particulate additive in the product or layer is usually at least 0.2% by weight of the product in order to give a useful increase in performance, and is generally at least about 0.4 or 0.5% by weight. Preferably it is at least 1% by weight.
  • the amount is generally not more than 15%, preferably not more than 10%. It can be not more than 6%. For rock, stone or slag wool fibres in particular the amount is preferably lower. In this case the amount is preferably not more than 10%, more preferably not more than 7% or 6%.
  • Preferred amounts are from 0.5 to 10%, preferably 1 to 6% by weight of the product.
  • the MMV fibres can be any man-made vitreous fibres which are suitable for the production of low density thermal insulation. Accordingly the fibres can be glass, rock, stone or slag fibres. The fibres can have any suitable dimensions, for instance those which are conventional in the production of low density and thermal insulation products. Generally the average fibre diameter is below 10 ⁇ m, eg below 5 ⁇ m, and can be the same as conventional fibre diameter or less.
  • Particle size can be measured by a laser scattering technique. Suitable equipment for such techniques include those available from, e.g., Malvern Instruments and Sympatec Helos.
  • the laser scattering technique provides various size and size distribution properties.
  • the average particle size is the volume median diameter, often described as d 50 . This is the median value in the volume distribution calculated by the laser scattering method. This value is commonly used by suppliers of particulate materials to denote average particle size.
  • this average particle size is not more than 100 ⁇ m, more preferably not more than 20 ⁇ m and in particular not more than 10 ⁇ m, especially not more than 5 ⁇ m. Particularly good results can be achieved with particles of average size not more than 4 ⁇ m, and in particular not more than 3 ⁇ m.
  • the average particle size is usually at least 0.01 ⁇ m and generally at least 0.1 or 0.5 ⁇ m. Best results are generally obtained when the average particle size is between about 0.5 and 10 ⁇ m, preferably about 1 to 3 or 4 ⁇ m.
  • the d 90 value (ie 90% of the particles in the volume distribution are below this value) is not more than 20 ⁇ m, in particular not more than 10 ⁇ m, preferably not more than 8 ⁇ m. Particularly good results can be achieved when d 90 is not more than 6 ⁇ m.
  • d 10 (ie 10% of particles in the volume distribution are below this value) is at least O.l ⁇ , more preferably at least 0.5 ⁇ m, in particular at least 0.8 or l ⁇ m.
  • surface area can be calculated from the laser scattering measurements obtained by the above methods. In this case, surface area is generally above 0.1 m 2 /g, preferably above 0.5 m 2 /g. Preferably it is at least 0.8 2 /q . It may range up to 10 irr/g or higher.
  • An alternative and preferred method for measuring surface area is the well known BET method. This provides a specific surface area value.
  • the surface area is generally above 0.5 m 2 /g, preferably above 1 m 2 /g. More preferably it is at least 5 m 2 /g, most preferably at least 10 m 2 /g. It may range up to 20 m 2 /g or higher, and is preferably not more than 30 irr/g, more preferably not more than 20 m 2 /g.
  • the particulate additive comprises aluminium, or mica, these may be in the form of powder or, preferably, flakes. These generally have surface area of from 2 to 10 m 2 /g (BET) .
  • the other additives are preferably in the form of powder.
  • the additives, especially silicon may be coated, for instance with acrylic polymer.
  • the batt or granulate generally consists substantially only of MMV fibres, the particulate additives, binder and minor additives such as oil. It is usually free of combustible or organic fibres.
  • the granulate or batt, and (in a batt product) the or each layer which consists of part or all of the thickness of the batt, must be low density, and in practice usually has a density of below 300 kg/m 3 and preferably below 150, and most preferably below 120 kg/m 3 . Density is usually at least 5, preferably at least 7 kg/m 3 . Preferably it is from 10 to 150 kg/m 3 .
  • the density is 60 kg/m 3 or less, for instance not more than 40 kg/m 3 , in particular not more than 30 kg/m 3 .
  • Suitable applications for materials having density in this range are general building insulation.
  • the invention can thus be beneficial in applications in which the product is required to have very low density, such as flight insulation (eg from 10 to 20 kg/m 3 ) .
  • the density may be below 10 kg/m 3 , for instance from 5 to 8 kg/m 3 .
  • the invention also gives benefits in products having density greater than about 40 kg/m 3 and these include building insulation products where high strength is required, lamellar products and technical insulation.
  • An advantage of the invention is that it may be applied at a wide range of temperatures.
  • the products may be used for high temperature insulation above 300°C, for instance up to 500 or 800°C.
  • the products are also useful for improving insulation properties at low temperatures, for instance down to -80°C, for instance down to -20°C. It is particularly beneficial and surprising that the additives give improved insulation across this entire range.
  • One preferred range for use in the invention is from -80°C to 30°C. Products of the invention can be used at such temperatures in applications such as flight insulation and cold storage.
  • the invention is also useful for applications such as building insulation, and technical insulation (e.g. insulation of pipes for hot water or ventilation) at temperatures of from -30 to 100°C.
  • a further range of high temperatures at which the invention is useful is from 80 to 300°C.
  • Suitable applications include technical insulation (.e.g. for boilers and steam pipes) .
  • the invention may especially be used to give effective insulation at temperatures above 300°C, for instance up to 500°C and even up to 800°C.
  • Suitable amounts of binder are 0.1 to 20 or 10%, generally 0.5 to 7%, preferably 1 to 5%, by weight binder solids based on the dry weight of the product.
  • the binder is applied as an aqueous solution and the additive can be included as a suspension in this solution.
  • the binder for the additive can be inorganic such as sodium or potassium or lithium silicate, silicophosphate, monoaluminium phosphate or silica sol.
  • the binder for the additive is organic and can be any of the conventional curable binders which are known for MMVF batts.
  • Suitable binders include curable and non- curable binders and examples are those based on phenol, urea, resorcinol, furanic binders or melamine, and in particular resins formed by reacting the above with formaldehyde.
  • Curable and non-curable acrylic binders, polyvinyl acetate, polyamides, polyimides, polyamides/- imides, polyesters, modified starches, chitosan, dopa, tannin, xanthan and other gums, cellulose derivatives, alginates, thermoplastics and mixtures thereof may be used.
  • the amount of organic binder is usually not more than 20%, preferably not more than 10%, and generally not more than 7%, with preferred amounts being below 5%. These percentages are by weight binder solids based on the dry weight of the product. Inorganic and organic binders may also be used in combination.
  • the additive can be included as a suspension in the aqueous binder.
  • the dry weight of total binder in the final batt is preferably below 10%, usually below 7%, and more preferably below 4 or 5% by weight.
  • the amounts of binder which are used are slightly greater than those which would be required for equivalent products without the selected additive.
  • additional binder in an amount of around 0.1 to 1, preferably 0.1 to 0.5, more preferably 0.2 to 0.3 (eg about 0.25) parts binder per part additive is required in addition to the standard amount which would be used in the absence of additive.
  • Total amounts of binder are often at least 0.5 or 1% by weight of the total product.
  • they may be and preferably are randomly oriented within the product and, if the product is a batt, within the or each layer or the batt.
  • the thermal insulation product may consist solely of the batt or granulate. Thus it can consist of either the batt containing the particulate additive distributed throughout its thickness or a batt stratum which contains particulate additive and which is integral with the remainder of a batt which is otherwise free of particulate additive.
  • a batt product can comprise other materials, for instance one or more other air-laid MMVF batts and/or decorative or structural materials such as foil.
  • bath includes very flexible roll products such as those used for insulation for pipes or boiler insulation, as well as less flexible (or even inflexible) products, for instance those in the form of slabs.
  • the batt product can be shaped in conventional shapes, for instance pipe sections for use as insulation for pipes or for boiler installations or for general building insulation. Accordingly, the product can have shapes such as cylindrical, part cylindrical or substantially rectangular slabs and rolls.
  • the invention is also useful when the product is not in the form of a batt but is in the form of granulated material such as is used for general building insulation. These materials are generally formed by granulating preformed batts and are thus produced by a process comprising formation of a batt.
  • the products of the invention are particularly beneficial in thermal insulation applications, they may also be used in other applications for which MMVF products are known, for instance fire protection and prevention and acoustic insulation.
  • the batt can be made in conventional manner, for instance by forming a cloud of man-made vitreous fibres entrained in air by fiberising mineral melt into an air stream and air-laying the fibres on to a collector as a web, and converting the web to a batt in conventional manner. This conversion can involve, for instance, cross- lamination of the web and drying, melting or curing of any binder that is present.
  • particulate additive can be distributed through some or all of the thickness of the eventual batt by including it in part or all of the cloud of fibres as they are formed and collected. Depending on how the particulate additive is distributed within the cloud, it will then be distributed uniformly throughout the web or will be distributed through part only of the web. It is then possible, in conventional manner, to form a batt which either has particulate additive distributed throughout its thickness or through part only of its thickness. Suitable systems include those described in our International Patent Application number PCT/EP99/02149.
  • the additive can be included in the cloud of fibres either by injecting it into the cloud, either from around or from within the cloud, or by injecting the additive into the cloud during the formation of the fibres.
  • the mineral melt is generally fiberised using either a centrifugal fiberising apparatus such as a disk or cup which rotates about a substantially vertical axis or a cylinder or disk which rotates about a substantially horizontal axis. In the latter case it is usually a cascade of cylinders which is used. This initially forms an annular cloud of fibres, and the additive can be injected into this annular cloud from the centrifugal fiberising apparatus.
  • a centrifugal fiberising apparatus such as a disk or cup which rotates about a substantially vertical axis or a cylinder or disk which rotates about a substantially horizontal axis.
  • a centrifugal fiberising apparatus such as a disk or cup which rotates about a substantially vertical axis or a cylinder or disk which rotates about a substantially horizontal axis.
  • a cascade of cylinders which is used.
  • Finer particles may be distributed using a conventional centrifugal distribution means which is attached to and rotates coaxially with one or more of the cylinders, or via spray nozzles placed inside or outside the annular cloud (such as are used as conventional binder supply nozzles) .
  • This process of the invention is especially beneficial because the particulate additive is added in simple and convenient manner. There is no need to devise additional processing steps, for instance for arranging the particles in the product (as is necessary in US 4,919,995). Furthermore, uniform and homogeneous distribution of the additive is promoted by its inclusion during formation of the fibres, rather than after collection (as in US 3,014,872) .
  • the additive may be added as a powder or as a slurry in water or as a slurry in aqueous binder.
  • the aqueous binder may be the binder for the batt or a separate aqueous binder solution. Part of the additive may be added with the binder for the batt and part added with a separate binder solution.
  • the additive is added as a slurry in a liquid in which is included a dispersing agent.
  • the amount of dispersing agent in the slurry is 0.1 to 2%, preferably 0.1 to 1.0%, dry weight dispersing agent based on weight of slurry.
  • the slurry can also include defoamer (antifoaming agent) in an amount of from 0.01 to 2 wt %, preferably 0.1 to 1.0 wt %, by weight of slurry, and/or 0.05 to 1 wt %, preferably 0.1 to 0.5 wt %, by weight of slurry, of anti- settling agent.
  • defoamer anti-settling agent
  • the amount of additive in the slurry is from 10 to 60%, preferably 20 to 50% by weight additive based on weight of slurry.
  • the additive is added with the binder for the product a slurry of this concentration is generally first produced and then mixed with the binder for the product. In that case, the eventual amount of additive in the slurry applied to the fibres may be as low as 0.5% but is often at least 0.8% and preferably at least 2%.
  • Another (less preferred) way of making the products of the invention is by collecting the web of fibres (without prior addition of additive) and then impregnating the additive into the web, for instance on the collector, and then converting the web to a batt.
  • Another way of making the products is by forming a batt in conventional manner, for instance as described above, and then impregnating part or all of the thickness of the batt with the additive. This method is less preferred, as uniform distribution can be difficult to obtain, except for thin layers.
  • the additive may be added as powder or as a slurry in water or as a slurry in aqueous binder (either the binder for the batt or a separate aqueous binder solution) . It is essential that the additive is bonded to the surfaces of the fibres.
  • the proportion of additive in the final product is usually slightly lower than the proportion included in the process (wt.% based on fibres forming) .
  • the proportion included in the process is approximately 1.3 times the final proportion required in the product, ie about 75% of the amount added appears in the product.
  • the additives may be included by the process described in our co-pending Application No. PCT/EP99/... (reference PRL04286GB) , the disclosure of which is incorporated herewith by reference.
  • the additive is included using apparatus comprising a set of at least three rotors mounted on a housing each for rotation about a different substantially horizontal axis and arranged such that when the rotors are rotating melt poured onto the periphery of the top rotor in the set is thrown onto the periphery of each subsequent rotor in turn and fibres are thrown off the rotors, air supply means for blowing the fibres axially along the chamber and which comprise a primary air supply slot associated with each subsequent rotor wherein each slot has an internal diameter substantially the same as the external diameter of the periphery of its associated rotor and is constructed for discharging a primary air blast substantially parallel to that periphery as a wall jet, and additive supply means on or adjacent the spinner, preferably at least one additive discharge orifice on each (or any) of the subsequent rotors positioned within the periphery of the rotor and rotating with the rotor, for spraying additive outwardly onto the fibres as they are thrown
  • the additive and the product may have any of the preferred features discussed above. We find that this process provides even greater improvements in ⁇ value.
  • Typical products of the invention made from rock, stone or slag wool by centrifugal fiberising apparatus
  • the products of the invention may also contain (bonded to the MMVF product) graphite particles in addition to the additives defined above.
  • graphite is described in our co-pending Application No. PCT/EP99/... (reference PRL04151GB) and its disclosure is incorporate herein.
  • Preferred ratios of graphite: other additives are 1:99 to 50:50, more preferably 5:95 to 40:60.
  • Example 1 The following are examples. Example 1
  • 73 kg of a 20% aqueous, phenolic curable binder is mixed with 77 1 tap water followed by 1.4 kg dispersing agent which is a sodium salt of maleic acid-olefin copolymer (available from BASF under the tradename Pigmentverteiler MD 20) and 0.4 kg defoamer which is an aromatic mineral oil with added silica and acrylic polymer (available from Henkel-Nopco under the tradename NOPCO 8034-M) .
  • the liquid is slowly mixed for 5 min. 51 kg particulate additive is slowly added while stirring. The rate of stirring is increased and the batch is dispersed for 15 min. This dispersion is stable for several days.
  • a mineral melt is fiberised using a cascade spinner of conventional type having at least three substantially cylindrical rotors mounted for rotation about a horizontal axis, whereby melt poured onto the top rotor is thrown from one rotor to the next in series and is fiberised.
  • An airstream flows from the rotors in conventional manner to carry the fibres as a cloud towards a permeable inclined collector, where the fibres are collected as a web in conventional manner.
  • the aqueous binder and additive slurry is injected into the cloud as it is formed using the conventional binder supply tubes on the fibre forming apparatus.
  • Example 2 Various tests are carried out using different particulate additives, added using a process essentially as in Example 1. In the reference test no additive was included. In Test 1 , 6 wt.% (added based on amount of wool produced) Si0 2 (average size 0.15 ⁇ m, surface area 20 m 2 /g by BET) is added to the product. In Test 2 , 4 wt.% (added based on total wool produced) Ti0 2 (average size 3 ⁇ m) is added.
  • Test 3 4.5 wt.% (added based on total wool produced) silicon (average size 3.5 ⁇ m, surface area 1.1 m 2 /g by laser scattering) is added.
  • Test 4 4 wt.% (based on total wool produced) mica (average size 5 ⁇ m, surface area 8.4 m ⁇ /g by laser scattering) is added.
  • Test 5 4 wt.% (based on total wool produced) aluminium powder (average size 6 ⁇ m, surface area 1.2 m 2 /g by laser scattering) is added. In each case, the proportion of additive in the final product is lower by a factor of about 0.75.
  • the thermal conductivity of each of the products was measured at 10°C in accordance with the ISO 8301 norm. Results are shown in Table 1. Table 1
  • the aqueous binder and silicon slurry is injected into the cloud of fibres as it is formed using the conventional binder supply tubes on the fibre forming apparatus.

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  • Compositions Of Macromolecular Compounds (AREA)
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Abstract

L'invention concerne des produits d'isolation thermique constitués d'une matière de fibres vitreuses air-laid comprenant un adjuvant particulaire distribué de façon homogène. Cet adjuvant particulaire est choisi dans le groupe constitué de silicium, d'aluminium, de mica, de silice et de dioxyde de titane. Les particules d'addition sont liées par un liant aux surfaces des fibres vitreuses. Ces produits peuvent se présenter sous forme granulée. De préférence, ces produits comprennent une couche qui se présente sous la forme d'un matelas isolant air-laid à base de fibres vitreuses comprenant du graphite distribué de façon homogène. L'ajout de graphite améliore les propriétés d'isolation thermique (valeur μ).
EP99948857A 1998-09-24 1999-09-24 Production de produits d'isolation thermique en matiere de fibres vitreuses Withdrawn EP1115674A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP99948857A EP1115674A1 (fr) 1998-09-24 1999-09-24 Production de produits d'isolation thermique en matiere de fibres vitreuses

Applications Claiming Priority (10)

Application Number Priority Date Filing Date Title
EP98307761A EP0989103A1 (fr) 1998-09-24 1998-09-24 Produits de fibres vitreuses artificielles pour isolation thermique et leur production
EP98307761 1998-09-24
GB9916176 1999-07-09
GBGB9916175.4A GB9916175D0 (en) 1999-07-09 1999-07-09 Man-made vitreous fibre products for use in thermal insulation, and their production
GBGB9916174.7A GB9916174D0 (en) 1999-07-09 1999-07-09 Man-made vitreous fibre products for use in thermal insulation, and their production
GB9916175 1999-07-09
GB9916174 1999-07-09
GBGB9916176.2A GB9916176D0 (en) 1999-07-09 1999-07-09 Man-made vitreous fibre products for use in thermal insulation, and their production
PCT/EP1999/007121 WO2000017121A1 (fr) 1998-09-24 1999-09-24 Production de produits d'isolation thermique en matiere de fibres vitreuses
EP99948857A EP1115674A1 (fr) 1998-09-24 1999-09-24 Production de produits d'isolation thermique en matiere de fibres vitreuses

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EP99947421A Expired - Lifetime EP1127032B1 (fr) 1998-09-24 1999-09-24 Production de produits d'isolation thermique en matiere de fibres vitreuses

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AT (1) ATE258537T1 (fr)
AU (2) AU6087499A (fr)
DE (1) DE69914501T2 (fr)
DK (1) DK1127032T3 (fr)
ES (1) ES2215403T3 (fr)
HU (2) HU224120B1 (fr)
WO (2) WO2000017121A1 (fr)

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DK1680561T3 (da) * 2003-10-06 2013-01-14 Saint Gobain Isover Isolationselement af mineralfibre til skibsbygning
US8178177B2 (en) 2005-02-11 2012-05-15 3M Innovative Properties Company Duct wrap and method for fire protecting a duct
PL1928796T3 (pl) * 2005-08-19 2017-10-31 Rockwool Int Sposób i urządzenie do wytwarzania wyrobów ze sztucznych włókien szklistych
EP2121533A1 (fr) * 2007-01-12 2009-11-25 Knauf Insulation GmbH Lutte contre l'électricité statique présente sur des fibres de verre par application de graphite
FR2929937B1 (fr) * 2008-04-11 2011-09-30 Electricite De France Produit d'isolation thermique a base de laine minerale et de poudre metallique a faible emissivite.
US9994482B2 (en) 2009-08-11 2018-06-12 Johns Manville Curable fiberglass binder
US9604878B2 (en) 2009-08-11 2017-03-28 Johns Manville Curable fiberglass binder comprising salt of inorganic acid
US9676954B2 (en) 2009-08-11 2017-06-13 Johns Manville Formaldehyde-free binder compositions and methods of making the binders under controlled acidic conditions
US9034970B2 (en) 2009-08-11 2015-05-19 Johns Manville Curable fiberglass binder comprising salt of inorganic acid
US8708162B2 (en) 2009-08-19 2014-04-29 Johns Manville Polymeric fiber webs with binder comprising salt of inorganic acid
US9365963B2 (en) 2009-08-11 2016-06-14 Johns Manville Curable fiberglass binder
DE102010036535A1 (de) 2010-07-21 2012-01-26 Saint-Gobain Isover G+H Ag Verfahren zum Metallisieren von Mineralfasern sowie Verwendung derselben
DE102010064103A1 (de) 2010-12-23 2012-06-28 SCHWENK DÄMMTECHNIK GMBH & Co KG Dämmmaterial
US8961675B2 (en) 2010-12-28 2015-02-24 Usg Interiors, Llc Acoustic building material employing chitosan
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DE102011121090A1 (de) 2011-12-14 2013-06-20 Saint-Gobain Isover G+H Ag Wärmedämmelement aus Mineralwolle, insbesondere Stein-oder Glaswolle
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AU6196399A (en) 2000-04-10
DE69914501T2 (de) 2004-11-04
AU6087499A (en) 2000-04-10
DE69914501D1 (de) 2004-03-04
WO2000017120A1 (fr) 2000-03-30
EP1127032B1 (fr) 2004-01-28
ATE258537T1 (de) 2004-02-15
HU224120B1 (hu) 2005-05-30
EP1127032A1 (fr) 2001-08-29
HUP0103850A3 (en) 2002-08-28
WO2000017121A1 (fr) 2000-03-30
DK1127032T3 (da) 2004-06-07
HUP0104152A2 (en) 2002-11-28
HUP0103850A2 (hu) 2002-02-28
ES2215403T3 (es) 2004-10-01

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