US20110089074A1 - Formaldehyde-free mineral fibre insulation product - Google Patents

Formaldehyde-free mineral fibre insulation product Download PDF

Info

Publication number
US20110089074A1
US20110089074A1 US12/940,601 US94060110A US2011089074A1 US 20110089074 A1 US20110089074 A1 US 20110089074A1 US 94060110 A US94060110 A US 94060110A US 2011089074 A1 US2011089074 A1 US 2011089074A1
Authority
US
United States
Prior art keywords
insulating material
mineral fiber
fiber insulating
mineral
organic
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.)
Abandoned
Application number
US12/940,601
Inventor
Roger Jackson
Tony Aindow
George Baybutt
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.)
Individual
Original Assignee
Individual
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=38611893&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20110089074(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Individual filed Critical Individual
Priority to US12/940,601 priority Critical patent/US20110089074A1/en
Publication of US20110089074A1 publication Critical patent/US20110089074A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04BGENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
    • E04B1/00Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
    • E04B1/62Insulation or other protection; Elements or use of specified material therefor
    • E04B1/74Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
    • E04B1/76Heat, 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
    • E04B1/7654Heat, 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 comprising an insulating layer, disposed between two longitudinal supporting elements, e.g. to insulate ceilings
    • E04B1/7658Heat, 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 comprising an insulating layer, disposed between two longitudinal supporting elements, e.g. to insulate ceilings comprising fiber insulation, e.g. as panels or loose filled fibres
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B30/00Compositions for artificial stone, not containing binders
    • C04B30/02Compositions for artificial stone, not containing binders containing fibrous materials
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-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
    • D04H1/42Non-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
    • D04H1/4209Inorganic fibres
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING 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
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-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
    • D04H1/58Non-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
    • D04H1/64Non-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
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/10Compositions or ingredients thereof characterised by the absence or the very low content of a specific material
    • C04B2111/1006Absence of well-defined organic compounds
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/16Two dimensionally sectional layer
    • Y10T428/161Two dimensionally sectional layer with frame, casing, or perimeter structure
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/16Two dimensionally sectional layer
    • Y10T428/163Next to unitary web or sheet of equal or greater extent
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity

Definitions

  • This invention relates to a mineral fibre insulating product having a low formaldehyde or formaldehyde free binder.
  • binders used for fibre insulation for example glass wool and rock wool insulation are based on phenol formaldehyde. Whilst such binders can provide suitable properties to the insulating products there has for some time been a desire to move away from the use of phenol formaldehyde, particularly due to environmental considerations.
  • the present invention provides a packaged mineral fibre insulating material as defined in claim 1 .
  • Other aspects are defined in other independent claims.
  • Preferred and/or alternative features are defined in the dependent claims.
  • formaldehyde free means that the composition is substantially free from formaldehyde, preferably does not liberate substantial formaldehyde as a result of drying or curing and/or preferably comprises less than one part per million by weight of formaldehyde.
  • Desired characteristics to be conferred by the binder on some mineral wool insulation product can be assessed by measuring Recovered Thickness and/or Ordinary Parting Strength and/or Weathered Parting Strength. The procedures for measuring these characteristics are set out below. This is particularly the case for low and medium density insulating products, for example, having a density in the range 5-40 kg/m 3 , for example roll insulation and/or glass wool thermal insulation for lofts and/or cavity walls.
  • Desired characteristics for some mineral wool insulation product can be assessed by measuring Ordinary Compression Strength and/or Weathered Compression Strength. The procedures for measuring these characteristics are set out below. This is particularly for higher density insulating products, for example, insulating 5 boards or materials adapted for use as: a fire barrier; a fire protection; cladding for a building; a ceiling tile; a roof board; thermal insulation for high temperature machinery for example, generators, ovens and industrial plant. Such products may be made of rock wool.
  • the pH of the binder when applied may be substantially neutral or alkaline; this may facilitate handling and avoid significant corrosion and/or environmental problems. Its pH when applied may be: greater than or equal to 7 and/or less than or equal to 10; between 7 and 10; between 8 and 10.
  • An important aspect of the invention is the pH of the binder in liquid form when applied to the fibres as this is the form in which the binder will have significant contact with manufacturing equipment as freshly prepared and in a wash water system.
  • the binder may change its pH as it cures; it may become more acidic as it cures. Nevertheless, once cured, the binder has less direct contact with the manufacturing equipment. Furthermore, where the cured binder is substantially insoluble in water, which is preferably the case, there is little risk of acid contamination from the cured binder.
  • binders of this type at 15% or less by weight can confer the desired characteristics on the insulating product.
  • This amount of binder is comparable with the binder contents commonly used with phenol formaldehyde based binders.
  • the cured binder content may be 12% or less or 10% or less; it may be within the range of 3-8%, particularly 3.5-6% by weight.
  • the binder content may be determined by loss on ignition. Such binder contents are particularly suitable for low and medium density products. Particularly for higher density products, the cured binder content may be in the range 0.5-5% by weight.
  • the binder may:
  • the binder may be based on a combination of a polycarboxylic acid, for example citric acid, a sugar, for example dextrose, and a source of ammonia, for example ammonia solution. It may be based on a combination of ammonium citrate and dextrose.
  • a polycarboxylic acid for example citric acid
  • sugar for example dextrose
  • ammonia solution for example ammonia solution
  • ammonia solution for example ammonia solution. It may be based on a combination of ammonium citrate and dextrose.
  • the binder is based on sugars and/or citric acid and or comprises significant —OH groups, it is particularly surprising that such levels of Weathered Parting Strength can be achieved. It would have been thought that the —OH groups for example in the sugars and/or citric acid would be readily subject to hydrolysis and that the binder would consequently loose significant strength in humid and/or weathering conditions.
  • the binder may comprise a silicon containing compound, particularly a silane; this may be an amino-substituted compound; it may be a silyl ether; it may facilitate adherence of the binder to the mineral fibres.
  • the binder may comprise melanoidins; it may be a thermoset binder; it may be thermally curable.
  • the binder may be one of those disclosed in International patent application No. PCT/US2006/028929, the contents of which is hereby incorporated by reference.
  • the insulating material may be packaged or be provided in the form of a package; the package may comprise one or more mineral wool insulating products arranged and/or bound together, for example to facilitate transport; it may comprise an enveloping film, for example of a plastics material.
  • the package may comprise or consist of a roll of insulating material or an assembly of individual slabs of insulating material.
  • the insulating material particularly when it is a low or medium density product, may have
  • the insulating material particularly when it is an insulating board or a higher density product, may have
  • the mineral fibres may be glass wool or rock wool; the fibres may have an average diameter between 2 and 9 microns or be microfibres of smaller diameter; they may have an average length between 8 and 80 mm.
  • the mineral fibres may be crimped.
  • the present invention provides a mineral fibre insulating material having at least one of the following features:
  • the insulating material may have any combination of these features; these features may be combined with other features and/or aspects described herein.
  • FIG. 1 shows the form of samples used for testing parting strength.
  • An aqueous binder was prepared by mixing together:
  • This binder was used in the manufacture of a fibre glass insulating product on a standard manufacturing line, the binder being sprayed onto glass fibres just after fiberising using internal spinners and the coated fibres being collected, assembled in to a mat and cured in the usual way.
  • the binder had a pH of about 8 when applied to the glass fibres.
  • the cured glass fibre insulating product had:
  • Thickness is tested and measured in accordance with Annex A of British standard BS EN 823: 1995 (incorporated herein by reference) and expressed as a % of the nominal or announced thickness for the product measured.
  • Parting strength is a measure of the tensile strength of mineral fibre mats determined by placing an O shaped sample over cylindrical jaws, separating the jaws and measuring the load to break the fibres. Although it can be measured in Newtons per gram, the parting strength is expressed in grams/gram being the total breaking load of six test specimens divided by their total weight.
  • the test is carried out on mineral fibre mats as received for testing (Ordinary Parting Strength) and after an accelerated weathering test as explained below (Weathered Parting Strength).
  • a first set of six samples of the form and dimensions shown in FIG. 1 are cut from the mineral fibre mat to be tested; the long axis of the samples should be parallel to the conveyor direction and the samples should be taken across the full width of the mineral mat.
  • a second set of six samples is then taken in the same way.
  • the dimensions in FIG. 1 are in mm.
  • the total weight of the first group of six samples W 1 in grams is recorded.
  • the total weight of the second group of six samples W 2 in grams is recorded; these samples are then placed in a preheated autoclave and conditioned on a wire mesh shelf away from the bottom of the chamber under wet steam at 35 kN/m 2 for one hour. They are then removed, dried in an oven at 100° C. for five minutes and tested immediately for parting strength.
  • each sample is mounted in turn on the jaws of the tensile strength machine and the maximum breaking load in grams or Newtons is recorded. If the breaking load is measured in Newtons it is converted to grams by multiplying it by 101.9. Six results in grams are obtained for each set of samples: G 1 G 2 G 3 G 4 G 5 and G 6 for the first set of samples and G 7 G 8 G 9 G 10 G 11 and G 12 for the second set of samples.
  • an aqueous binder was prepared by mixing together:
  • This binder was used in the manufacture of a rock wool roof board on a standard manufacturing line, the binder being sprayed onto the fibres just after fiberising and the coated fibres being collected, assembled in to a mat, compressed and cured in the usual way.
  • the cured roof board had:
  • Weathered Compression Strength is measured according to British Standard BS EN 826: 1996 on samples that have been subjected to the following accelerated weathering procedure: samples are cut to size and then placed in a preheated autoclave and conditioned on a wire mesh shelf away from the bottom of the chamber under wet steam at 35 kN/m 2 for one hour. They are then removed, dried in an oven at 100° C. for five minutes and tested immediately for compression strength.
  • compression strength is determined in the direction of the thickness of the product; the dimensions of face of the samples in contact with the compression test apparatus are preferably 200 mm ⁇ 200 mm.

Abstract

A packaged mineral fibre insulating material has: a) a Recovered Thickness of at least 95% nominal thickness; and b) an Ordinary Parting Strength of at least 95 g/g; and c) a Weathered Parting Strength of at least 75 g/g the material comprising mineral fibres and an organic, formaldehyde free binder in a quantity of less than 15% by weight, preferably less than 10% by weight, said binder having been applied to the fibres of the insulating material in liquid form at pH of greater than 5.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation of U.S. patent application Ser. No. 12/524,491, filed Nov. 12, 2009, which is a U.S. national counterpart application of application serial no. PCT/EP2007/050750 filed Jan. 25, 2007.
  • FIELD OF THE INVENTION
  • This invention relates to a mineral fibre insulating product having a low formaldehyde or formaldehyde free binder.
  • BACKGROUND
  • Industry standard binders used for fibre insulation, for example glass wool and rock wool insulation are based on phenol formaldehyde. Whilst such binders can provide suitable properties to the insulating products there has for some time been a desire to move away from the use of phenol formaldehyde, particularly due to environmental considerations.
  • Traditional polyester based binder systems have previously been proposed but have not gained acceptance in the insulation industry, particularly as their strength in holding the mineral fibres together, especially when exposed to moisture or weathering, has been perceived as insufficient.
  • To date, only one low formaldehyde based mineral insulation binder system has been used on an industrial scale on glass wool insulation; this is based on polyacrylic acid and supplied by Rohm & Haas. Unfortunately, the highly acid nature of these types of binders can cause excessive corrosion of manufacturing plant unless significant investment is made in acid resistant equipment. U.S. Pat. No. 5,977,232 discloses a formaldehyde free binder for glass wool insulation based on a polycarboxylic acid. European patent application EP1698598A discloses use of a corrosion meter to try to mitigate problems associated with polycarboxylic acid-based fibreglass binder resins. In addition, whilst the strength of these binders is acceptable for some applications it is not as good as the commonly used phenol formaldehyde based binders.
  • It has not been thought possible to provide a formaldehyde free binder system useable on an industrial scale that will confer required characteristics, including strength, to mineral wool insulating products without encountering the difficulties associated with highly acidic liquid binder systems.
  • SUMMARY
  • According to one aspect, the present invention provides a packaged mineral fibre insulating material as defined in claim 1. Other aspects are defined in other independent claims. Preferred and/or alternative features are defined in the dependent claims.
  • DETAILED DESCRIPTION
  • As used herein, the term formaldehyde free means that the composition is substantially free from formaldehyde, preferably does not liberate substantial formaldehyde as a result of drying or curing and/or preferably comprises less than one part per million by weight of formaldehyde.
  • Desired characteristics to be conferred by the binder on some mineral wool insulation product can be assessed by measuring Recovered Thickness and/or Ordinary Parting Strength and/or Weathered Parting Strength. The procedures for measuring these characteristics are set out below. This is particularly the case for low and medium density insulating products, for example, having a density in the range 5-40 kg/m3, for example roll insulation and/or glass wool thermal insulation for lofts and/or cavity walls.
  • Desired characteristics for some mineral wool insulation product can be assessed by measuring Ordinary Compression Strength and/or Weathered Compression Strength. The procedures for measuring these characteristics are set out below. This is particularly for higher density insulating products, for example, insulating 5 boards or materials adapted for use as: a fire barrier; a fire protection; cladding for a building; a ceiling tile; a roof board; thermal insulation for high temperature machinery for example, generators, ovens and industrial plant. Such products may be made of rock wool.
  • The pH of the binder when applied may be substantially neutral or alkaline; this may facilitate handling and avoid significant corrosion and/or environmental problems. Its pH when applied may be: greater than or equal to 7 and/or less than or equal to 10; between 7 and 10; between 8 and 10.
  • An important aspect of the invention is the pH of the binder in liquid form when applied to the fibres as this is the form in which the binder will have significant contact with manufacturing equipment as freshly prepared and in a wash water system. The binder may change its pH as it cures; it may become more acidic as it cures. Nevertheless, once cured, the binder has less direct contact with the manufacturing equipment. Furthermore, where the cured binder is substantially insoluble in water, which is preferably the case, there is little risk of acid contamination from the cured binder.
  • It is surprising that binders of this type at 15% or less by weight can confer the desired characteristics on the insulating product. This amount of binder is comparable with the binder contents commonly used with phenol formaldehyde based binders. The cured binder content may be 12% or less or 10% or less; it may be within the range of 3-8%, particularly 3.5-6% by weight. The binder content may be determined by loss on ignition. Such binder contents are particularly suitable for low and medium density products. Particularly for higher density products, the cured binder content may be in the range 0.5-5% by weight.
  • The binder may:
      • be based on a reducing sugar; and/or
      • be based on reductosis; and/or
      • be based on an aldehyde containing sugars/and/or
      • include at least one reaction product of a carbohydrate reactant and an amine reactant; and/or
      • include at least one reaction product of a reducing sugar and an amine reactant; and/or
      • include at least one reaction product of a carbohydrate reactant and a polycarboxylic acid ammonium salt reactant; and/or
      • include at least one reaction product from a Maillard reaction.
  • The binder may be based on a combination of a polycarboxylic acid, for example citric acid, a sugar, for example dextrose, and a source of ammonia, for example ammonia solution. It may be based on a combination of ammonium citrate and dextrose. Where the binder is based on sugars and/or citric acid and or comprises significant —OH groups, it is particularly surprising that such levels of Weathered Parting Strength can be achieved. It would have been thought that the —OH groups for example in the sugars and/or citric acid would be readily subject to hydrolysis and that the binder would consequently loose significant strength in humid and/or weathering conditions.
  • The binder may comprise a silicon containing compound, particularly a silane; this may be an amino-substituted compound; it may be a silyl ether; it may facilitate adherence of the binder to the mineral fibres.
  • The binder may comprise melanoidins; it may be a thermoset binder; it may be thermally curable.
  • The binder may be one of those disclosed in International patent application No. PCT/US2006/028929, the contents of which is hereby incorporated by reference.
  • The insulating material may be packaged or be provided in the form of a package; the package may comprise one or more mineral wool insulating products arranged and/or bound together, for example to facilitate transport; it may comprise an enveloping film, for example of a plastics material. The package may comprise or consist of a roll of insulating material or an assembly of individual slabs of insulating material.
  • The insulating material, particularly when it is a low or medium density product, may have
      • a nominal thickness in the range 60-260 mm; and/or
      • a thermal resistance R of R≧3 m2K/W, preferably R≧4 m2K/W at a thickness or 200 mm; and/or
      • a density in the range 5-40 kg/m3, particularly 5-18 kg/m3 or 7-12 kg/m3, for example for low density roll products.
  • The insulating material, particularly when it is an insulating board or a higher density product, may have
      • a nominal thickness in the range 20 to 200 mm; and/or
      • a thermal resistance R of R≧1.7 m2K/W, preferably R≧2 m2K/W at a thickness of 100 mm; and/or
      • a density in the range 100 to 200 kg/m3, particularly 130 to 190 kg/m3.
  • The mineral fibres may be glass wool or rock wool; the fibres may have an average diameter between 2 and 9 microns or be microfibres of smaller diameter; they may have an average length between 8 and 80 mm.
  • The mineral fibres may be crimped.
  • According to a further aspect, the present invention provides a mineral fibre insulating material having at least one of the following features:
      • the insulating material having cut edges;
      • the insulating material having a facing provided on at least one of its major surface, for example comprising a moisture penetration barrier and/or a Kraft paper and/or an aluminium foil and/or a plastics layer and/or a laminate sheet comprising a plurality of individual layers and/or a woven or non-woven fabric; a facing may be provided on each major surface of the insulating material;
      • the insulating material being a packaged insulating material held under compression for example by one or more packaging components, for example by an enveloping packaging film; the insulating material may be compressed to 80% or less of its non-compressed thickness;
      • the insulating material being in the form of pipe insulation having a length of greater than 30 cm; the cross-section may be substantially annular;
      • the insulating material being in the form of a compressed roll of material;
      • the insulating material being in the form of a compressed slab of material;
      • the insulating material being a roll or slab having a length of greater than or equal to 1 m, preferably greater than or equal to 2 m;
      • the insulating material being a roll or slab having a width of greater than or equal to 0.3 m, preferably greater than or equal to 0.5 m;
      • the insulating material having a nominal thickness of at least 45 mm, preferably at least 50 mm, and a density in the range 5-40 kg/m3.
  • The insulating material may have any combination of these features; these features may be combined with other features and/or aspects described herein.
  • Examples
  • Non-limiting examples of the invention are described below with reference to FIG. 1 which shows the form of samples used for testing parting strength.
  • An aqueous binder was prepared by mixing together:
  • Approximate %
    by weight
    Powdered dextrose monohydrate 12.9%
    Powdered anhydrous citric acid  2.3%
    28% aqueous ammonia  2.6%
    Silane A-1100 0.05%
    water 82.1%
  • This binder was used in the manufacture of a fibre glass insulating product on a standard manufacturing line, the binder being sprayed onto glass fibres just after fiberising using internal spinners and the coated fibres being collected, assembled in to a mat and cured in the usual way.
  • The binder had a pH of about 8 when applied to the glass fibres.
  • The cured glass fibre insulating product had:
      • a binder content of about 5% by weight as determined by loss on ignition
      • a thickness of about 150 mm
      • a density of about 9 kg/m3
  • This is suitable as a low density residential roll insulation product; it was packaged in a roll under compression.
  • Desired characteristics and results achieved are set out in Table 1:
  • TABLE 1
    Accept-
    ance Pre- More Most Result
    Units Limit ferred Preferred Preferred Achieved
    Recovered % of ≧95 ≧100 ≧110 ≧120 103
    Thickness nominal
    Ordinary g/g ≧95 ≧100 ≧150 ≧200 122
    Parting
    Strength
    Weathered g/g ≧75 ≧80 ≧100 ≧150 112
    Parting
    Strength
  • Testing of Recovered Thickness:
  • Recovered Thickness is tested and measured in accordance with Annex A of British standard BS EN 823: 1995 (incorporated herein by reference) and expressed as a % of the nominal or announced thickness for the product measured.
  • Testing of Ordinary Parting Strength and Weathered Parting Strength:
  • Parting strength is a measure of the tensile strength of mineral fibre mats determined by placing an O shaped sample over cylindrical jaws, separating the jaws and measuring the load to break the fibres. Although it can be measured in Newtons per gram, the parting strength is expressed in grams/gram being the total breaking load of six test specimens divided by their total weight.
  • The test is carried out on mineral fibre mats as received for testing (Ordinary Parting Strength) and after an accelerated weathering test as explained below (Weathered Parting Strength).
  • A first set of six samples of the form and dimensions shown in FIG. 1 are cut from the mineral fibre mat to be tested; the long axis of the samples should be parallel to the conveyor direction and the samples should be taken across the full width of the mineral mat. A second set of six samples is then taken in the same way. The dimensions in FIG. 1 are in mm.
  • The total weight of the first group of six samples W1 in grams is recorded.
  • The total weight of the second group of six samples W2 in grams is recorded; these samples are then placed in a preheated autoclave and conditioned on a wire mesh shelf away from the bottom of the chamber under wet steam at 35 kN/m2 for one hour. They are then removed, dried in an oven at 100° C. for five minutes and tested immediately for parting strength.
  • To test the parting strength, each sample is mounted in turn on the jaws of the tensile strength machine and the maximum breaking load in grams or Newtons is recorded. If the breaking load is measured in Newtons it is converted to grams by multiplying it by 101.9. Six results in grams are obtained for each set of samples: G1 G2 G3 G4 G5 and G6 for the first set of samples and G7 G8 G9 G10 G11 and G12 for the second set of samples.
  • The Ordinary Parting Strength is calculated from the first set of samples using the formula Ordinary Parting Strength=(G1+G2+G3+G4+G5+G6)/W1.
  • The Weathered Parting Strength is calculated from the second set of samples using the formula Weathered Parting Strength=(G7+G8+G9+G10+G11+G12)/W2.
  • In another example, an aqueous binder was prepared by mixing together:
  • Approximate %
    by weight
    Powdered dextrose monohydrate 19.1%
    Powdered anhydrous citric acid  3.4%
    28% aqueous ammonia  2.6%
    Silane A-1100 0.07%
    water 73.5%
  • This binder was used in the manufacture of a rock wool roof board on a standard manufacturing line, the binder being sprayed onto the fibres just after fiberising and the coated fibres being collected, assembled in to a mat, compressed and cured in the usual way.
  • The cured roof board had:
      • a binder content of about 3% by weight as determined by loss on ignition
      • a thickness of about 80 mm
      • a density of about 150 kg/m3
  • It was packaged as part of a stack of insulation boards.
  • Desired characteristics and results achieved are set out in Table 2:
  • TABLE 2
    Accept-
    ance Pre- More Most Result
    Units Limit ferred Preferred Preferred Achieved
    Ordinary kPa ≧60 ≧70 ≧80 ≧90 72.3
    Compression
    Strength
    Weathered kPa ≧25 ≧30 ≧40 ≧50 54.6
    Compression
    Strength
  • Testing of Ordinary Compression Strength and Weathered Compression Strength:
  • Ordinary Compression Strength is measured according to British Standard BS EN 826: 1996 (incorporated herein by reference).
  • Weathered Compression Strength is measured according to British Standard BS EN 826: 1996 on samples that have been subjected to the following accelerated weathering procedure: samples are cut to size and then placed in a preheated autoclave and conditioned on a wire mesh shelf away from the bottom of the chamber under wet steam at 35 kN/m2 for one hour. They are then removed, dried in an oven at 100° C. for five minutes and tested immediately for compression strength.
  • In both cases, compression strength is determined in the direction of the thickness of the product; the dimensions of face of the samples in contact with the compression test apparatus are preferably 200 mm×200 mm.

Claims (20)

1. A mineral fiber insulating material comprising mineral fibers and less than about 15% by weight of an organic binder, wherein
a) the organic binder is a formaldehyde free product of curing an aqueous solution having a pH of greater than 5 when applied to the mineral fibers,
b) the mineral fiber insulating material has a recovered thickness of at least about 95% as determined according to Annex A of British standard BS EN 823: 1995,
c) the mineral fiber insulating material having an ordinary parting strength of at least about 95 g/g,
d) the mineral fiber insulating material having a weathered parting strength of at least about 75 g/g, and
e) the mineral fiber insulating material is packaged.
2. The mineral fiber insulating material of claim 1, wherein the recovered thickness is at least about 100%.
3. The mineral fiber insulating material of claim 1, wherein the ordinary parting strength is at least about 100 g/g.
4. The mineral fiber insulating material of claim 1, wherein the weathered parting strength is at least about 80 g/g.
5. The mineral fiber insulating material of claim 1, wherein the mineral fiber insulating material is a rolled product having a density between about 5 and about 40 kg/m3 and the mineral fiber insulating material is packaged under compression.
6. The mineral fiber insulating material of claim 1, wherein the organic, formaldehyde free binder is the product of drying and curing the aqueous solution with the pH being less than about 11 when applied to the mineral fibers.
7. The mineral fiber insulating material of claim 6, wherein the organic, formaldehyde free binder is the product of drying and curing the aqueous solution with the pH being between about 6 and about 10 when applied to the mineral fibers.
8. The mineral fiber insulating material of claim 1, wherein the organic, formaldehyde free binder is between about 2% and about 8% of the mineral fiber insulating material by weight.
9. The mineral fiber insulating material of claim 1, wherein the organic, formaldehyde free binder comprises a product of a reaction including a reducing sugar.
10. The mineral fiber insulating material of claim 1, wherein the organic, formaldehyde free binder comprises at least one Maillard reaction product.
11. A mineral fiber insulating material having a density in a range of 100 to 200 kg/m3 comprising mineral fibers and less than 15% by weight an organic, formaldehyde free binder, wherein
a) the mineral fiber insulating material has an ordinary compression strength of at least about 60 kPa,
b) the mineral fiber insulating material has a weathered compression strength of at least about 25 kPa,
c) the organic, formaldehyde free binder is a product of drying and curing an aqueous solution with a pH of greater than about 5 when applied to the mineral fibers, and
d) the mineral fiber insulating material is packaged.
12. The mineral fiber insulating material of claim 11, wherein the ordinary compression strength is at least about 70 kPa.
13. The mineral fiber insulating material of claim 11, wherein the weathered compression strength is at least about 30 kPa.
14. The mineral fiber insulating material of claim 11, wherein the organic, formaldehyde free binder is the product of drying and curing the aqueous solution with the pH being less than about 11 when applied to the mineral fibers.
15. The mineral fiber insulating material of claim 11, wherein the organic, formaldehyde free binder is the product of drying and curing the aqueous solution with the pH being between about 6 and about 10 when applied to the mineral fibers.
16. The mineral fiber insulating material of claim 11, wherein the organic, formaldehyde free binder is between about 2% and about 8% of the mineral fiber insulating material by weight.
17. The mineral fiber insulating material of claim 11, wherein the organic, formaldehyde free binder comprises a product of a reaction including a reducing sugar.
18. The mineral fiber insulating material of claim 11, wherein the organic, formaldehyde free binder comprises at least one Maillard reaction product.
19. The mineral fiber insulating material of claim 11, wherein the aqueous solution further comprises citric acid, ammonia and dextrose.
20. A method of manufacturing a packaged mineral fibre insulating material selected from the group consisting of:
(i) material having
a) a Recovered Thickness of at least 95%; and
b) an Ordinary Parting Strength of at least 95 g/g; and
c) a Weathered Parting Strength of at least 75 g/g; and
(ii) material having
a) an Ordinary Compression Strength of at least 60 kPa; and
b) a Weathered Compression Strength of at least 25 kPa;
comprising the steps of
i) applying an organic, formaldehyde free binder in aqueous solution to the mineral fibres at a pH of greater than 5 and
ii) curing the product so that it contains a quantity of less than 15% by weight of binder and
iii) packaging the insulating material.
US12/940,601 2007-01-25 2010-11-05 Formaldehyde-free mineral fibre insulation product Abandoned US20110089074A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US12/940,601 US20110089074A1 (en) 2007-01-25 2010-11-05 Formaldehyde-free mineral fibre insulation product

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
PCT/EP2007/050750 WO2008089851A1 (en) 2007-01-25 2007-01-25 Formaldehyde-free mineral fibre insulation product
US52449109A 2009-11-12 2009-11-12
US12/940,601 US20110089074A1 (en) 2007-01-25 2010-11-05 Formaldehyde-free mineral fibre insulation product

Related Parent Applications (2)

Application Number Title Priority Date Filing Date
PCT/EP2007/050750 Continuation WO2008089851A1 (en) 2007-01-25 2007-01-25 Formaldehyde-free mineral fibre insulation product
US52449109A Continuation 2007-01-25 2009-11-12

Publications (1)

Publication Number Publication Date
US20110089074A1 true US20110089074A1 (en) 2011-04-21

Family

ID=38611893

Family Applications (2)

Application Number Title Priority Date Filing Date
US12/524,491 Active US7854980B2 (en) 2007-01-25 2007-01-25 Formaldehyde-free mineral fibre insulation product
US12/940,601 Abandoned US20110089074A1 (en) 2007-01-25 2010-11-05 Formaldehyde-free mineral fibre insulation product

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US12/524,491 Active US7854980B2 (en) 2007-01-25 2007-01-25 Formaldehyde-free mineral fibre insulation product

Country Status (10)

Country Link
US (2) US7854980B2 (en)
EP (2) EP2126179B1 (en)
CN (1) CN101688343B (en)
BR (1) BRPI0721233A2 (en)
DK (2) DK2826903T3 (en)
ES (2) ES2945888T3 (en)
PL (2) PL2126179T3 (en)
PT (1) PT2126179E (en)
SI (2) SI2826903T1 (en)
WO (1) WO2008089851A1 (en)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100092785A1 (en) * 2004-10-13 2010-04-15 Helbing Clarence H Polyester binding compositions
US20110054143A1 (en) * 2004-03-11 2011-03-03 Helbing Clarence H Binder compositions and associated methods
US8900495B2 (en) 2009-08-07 2014-12-02 Knauf Insulation Molasses binder
US8901208B2 (en) 2007-01-25 2014-12-02 Knauf Insulation Sprl Composite wood board
US8940089B2 (en) 2007-08-03 2015-01-27 Knauf Insulation Sprl Binders
US20150053114A1 (en) * 2012-04-05 2015-02-26 Knauf Insulation Binders and associated products
US9040652B2 (en) 2005-07-26 2015-05-26 Knauf Insulation, Llc Binders and materials made therewith
US9309436B2 (en) 2007-04-13 2016-04-12 Knauf Insulation, Inc. Composite maillard-resole binders
US9492943B2 (en) 2012-08-17 2016-11-15 Knauf Insulation Sprl Wood board and process for its production
US9493603B2 (en) 2010-05-07 2016-11-15 Knauf Insulation Sprl Carbohydrate binders and materials made therewith
US9505883B2 (en) 2010-05-07 2016-11-29 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US9828287B2 (en) 2007-01-25 2017-11-28 Knauf Insulation, Inc. Binders and materials made therewith
US10508172B2 (en) 2012-12-05 2019-12-17 Knauf Insulation, Inc. Binder
US10767050B2 (en) 2011-05-07 2020-09-08 Knauf Insulation, Inc. Liquid high solids binder composition
US10864653B2 (en) 2015-10-09 2020-12-15 Knauf Insulation Sprl Wood particle boards
US10968629B2 (en) 2007-01-25 2021-04-06 Knauf Insulation, Inc. Mineral fibre board
US11060276B2 (en) 2016-06-09 2021-07-13 Knauf Insulation Sprl Binders
US11248108B2 (en) 2017-01-31 2022-02-15 Knauf Insulation Sprl Binder compositions and uses thereof
US11332577B2 (en) 2014-05-20 2022-05-17 Knauf Insulation Sprl Binders
US11401204B2 (en) 2014-02-07 2022-08-02 Knauf Insulation, Inc. Uncured articles with improved shelf-life
US11846097B2 (en) 2010-06-07 2023-12-19 Knauf Insulation, Inc. Fiber products having temperature control additives
US11939460B2 (en) 2018-03-27 2024-03-26 Knauf Insulation, Inc. Binder compositions and uses thereof
US11945979B2 (en) 2018-03-27 2024-04-02 Knauf Insulation, Inc. Composite products

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220267635A1 (en) * 2005-07-26 2022-08-25 Knauf Insulation, Inc. Binders and materials made therewith
SI2826903T1 (en) * 2007-01-25 2023-10-30 Knauf Insulation Method of manufacturing mineral fiber insulation product
FR2924719B1 (en) 2007-12-05 2010-09-10 Saint Gobain Isover SIZING COMPOSITION FOR MINERAL WOOL COMPRISING MONOSACCHARIDE AND / OR POLYSACCHARIDE AND POLYCARBOXYLIC ORGANIC ACID, AND INSULATING PRODUCTS OBTAINED
AU2010236595A1 (en) * 2009-04-13 2011-11-03 Owens Corning Intellectual Capital, Llc Soft fiber insulation product
US20110003522A1 (en) * 2009-05-15 2011-01-06 Liang Chen Bio-based aqueous binder for fiberglass insulation materials and non-woven mats
US9718729B2 (en) * 2009-05-15 2017-08-01 Owens Corning Intellectual Capital, Llc Biocides for bio-based binders, fibrous insulation products and wash water systems
FR2946352B1 (en) 2009-06-04 2012-11-09 Saint Gobain Isover MINERAL WOOL SIZING COMPOSITION COMPRISING A SACCHARIDE, A POLYCARBOXYLIC ORGANIC ACID AND A REACTIVE SILICONE, AND INSULATING PRODUCTS OBTAINED
WO2011002730A1 (en) * 2009-06-29 2011-01-06 Owens Corning Intellectual Capital, Llc Modified starch based binders
US20110223364A1 (en) 2009-10-09 2011-09-15 Hawkins Christopher M Insulative products having bio-based binders
WO2011044490A1 (en) 2009-10-09 2011-04-14 Owens Corning Intellectual Capital, Llc Bio-based binders for insulation and non-woven mats
US20140038485A1 (en) 2011-04-07 2014-02-06 Cargill Incorporated Bio-based binders including carbohydrates and a pre-reacted product of an alcohol or polyol and a monomeric or polymeric polycarboxylic acid
US20120309246A1 (en) 2011-06-03 2012-12-06 Alexander Tseitlin Curable biopolymer nanoparticle latex binder for mineral, natural organic, or synthetic fiber products and non-woven mats
US9957409B2 (en) 2011-07-21 2018-05-01 Owens Corning Intellectual Capital, Llc Binder compositions with polyvalent phosphorus crosslinking agents
US20150091209A1 (en) 2012-04-18 2015-04-02 Knauf Insulation Gmbh Molding apparatus and process
US8791198B2 (en) 2012-04-30 2014-07-29 H.B. Fuller Company Curable aqueous composition
US9416294B2 (en) 2012-04-30 2016-08-16 H.B. Fuller Company Curable epoxide containing formaldehyde-free compositions, articles including the same, and methods of using the same
EP2669349B1 (en) 2012-05-29 2014-06-04 Rohm and Haas Company Aqueous amine-carbohydrate thermosets having reduced weight loss upon cure and improved early dry strength
EP2679624A1 (en) 2012-06-29 2014-01-01 URSA Insulation, S.A. Formaldehyde-free binder and use for mineral wool insulation products
CA2894501C (en) * 2012-12-11 2020-01-14 Rockwool International A/S A method of forming a cured mineral fibre product
EP2969448B1 (en) 2013-03-13 2017-08-02 Knauf Insulation GmbH Molding process for insulation product
US11453798B2 (en) 2013-12-05 2022-09-27 Ecosynthetix Ltd. Formaldehyde free binder and multi-component nanoparticle
US9751289B2 (en) * 2014-11-10 2017-09-05 Knauf Insulation, Inc. Insulation articles including corrosion inhibitors and methods of producing the same
FR3033326B1 (en) * 2015-03-02 2018-10-26 Saint-Gobain Isover THERMODURCAL FOAMS AND METHOD OF MANUFACTURE
US9957380B2 (en) 2015-04-17 2018-05-01 Johns Manville Formaldehyde-free smoke reduction agents for binders
KR20210043374A (en) 2019-10-11 2021-04-21 주식회사 케이씨씨 Aqueous thermosetting composition for adhesive
KR102290676B1 (en) 2020-10-23 2021-08-19 주식회사 케이씨씨 Aqueous binder composition and fibrous materials using the same

Citations (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1801052A (en) * 1923-02-06 1931-04-14 Meigsoid Corp Resinous condensation product and process of making same
US1801053A (en) * 1925-01-22 1931-04-14 Meigsoid Corp Carbohydrate product and process of making same
US2393105A (en) * 1943-05-22 1946-01-15 Cook Electric Co Adapter
US3232821A (en) * 1964-12-11 1966-02-01 Ferro Corp Felted fibrous mat and apparatus for manufacturing same
US3802897A (en) * 1973-02-23 1974-04-09 Anheuser Busch Water resistant starch adhesive
US3809664A (en) * 1973-08-16 1974-05-07 Us Agriculture Method of preparing starch graft polymers
US3826767A (en) * 1972-01-26 1974-07-30 Calgon Corp Anionic dextran graft copolymers
US4028290A (en) * 1975-10-23 1977-06-07 Hercules Incorporated Highly absorbent modified polysaccharides
US4097427A (en) * 1977-02-14 1978-06-27 Nalco Chemical Company Cationization of starch utilizing alkali metal hydroxide, cationic water-soluble polymer and oxidant for improved wet end strength
US4107379A (en) * 1974-02-22 1978-08-15 John Stofko Bonding of solid lignocellulosic material
US4148765A (en) * 1977-01-10 1979-04-10 The Dow Chemical Company Polyester resins containing dicyclopentadiene
US4183997A (en) * 1974-02-22 1980-01-15 John Jansky Bonding of solid lignocellulosic material
US4246367A (en) * 1979-09-24 1981-01-20 United States Steel Corporation Dicyclopentadiene polyester resins
US4278573A (en) * 1980-04-07 1981-07-14 National Starch And Chemical Corporation Preparation of cationic starch graft copolymers from starch, N,N-methylenebisacrylamide, and polyamines
US4322523A (en) * 1978-07-28 1982-03-30 Bayer Aktiengesellschaft Methylolated mono- and oligosaccharides
US4330443A (en) * 1980-06-18 1982-05-18 The United States Of America As Represented By The Secretary Of Agriculture Dry chemical process for grafting acrylic and methyl acrylic ester and amide monomers onto starch-containing materials
US4400496A (en) * 1980-09-22 1983-08-23 University Of Florida Water-soluble graft copolymers of starch-acrylamide and uses therefor
US4464523A (en) * 1983-05-16 1984-08-07 National Starch And Chemical Corporation Process for the preparation of graft copolymers of cellulose derivatives and diallyl, dialkyl ammonium halides
US4524164A (en) * 1983-12-02 1985-06-18 Chemical Process Corporation Thermosetting adhesive resins
US4668716A (en) * 1983-09-30 1987-05-26 Union Carbide Corporation Novel fatty ethenoid acylaminoorganosilicon compounds and their use as a coupling agent
US4754056A (en) * 1985-04-05 1988-06-28 Desoto, Inc. Radiation-curable coatings containing reactive pigment dispersants
US4845162A (en) * 1987-06-01 1989-07-04 Allied-Signal Inc. Curable phenolic and polyamide blends
US4906237A (en) * 1985-09-13 1990-03-06 Astra Meditec Ab Method of forming an improved hydrophilic coating on a polymer surface
US4912147A (en) * 1987-10-14 1990-03-27 Basf Aktiengesellschaft Preparation of aqueous (meth)acrylate copolymer dispersions in two stages and their use as impregnating materials, coating materials and binders for sheet-like fibrous structures
US4923980A (en) * 1987-11-10 1990-05-08 Biocarb Ab Process for the manufacture of a gel product
US5037930A (en) * 1989-09-22 1991-08-06 Gaf Chemicals Corporation Heterocyclic quaternized nitrogen-containing cellulosic graft polymers
US5041595A (en) * 1990-09-26 1991-08-20 Union Carbide Chemicals And Plastics Technology Corporation Method for manufacturing vinylalkoxysilanes
US5095054A (en) * 1988-02-03 1992-03-10 Warner-Lambert Company Polymer compositions containing destructurized starch
US5106615A (en) * 1986-10-14 1992-04-21 Shabtay Dikstein Eyedrops having non-newtonian rheological properties
US5114004A (en) * 1990-02-14 1992-05-19 Material Engineering Technology Laboratory Inc. Filled and sealed, self-contained mixing container
US5124369A (en) * 1989-11-08 1992-06-23 Shell Oil Company Process for preparing soft flexible polyurethane foams and a polyol composition useful in said process
US5128407A (en) * 1991-07-25 1992-07-07 Miles Inc. Urea extended polyisocyanates
US5308896A (en) * 1992-08-17 1994-05-03 Weyerhaeuser Company Particle binders for high bulk fibers
US5318990A (en) * 1993-06-21 1994-06-07 Owens-Corning Fiberglas Technology Inc. Fibrous glass binders
US5336753A (en) * 1986-08-29 1994-08-09 Basf Lacke + Farben Ag Polycondensation and/or addition product containing carboxyl groups and tertiary amino groups, coating agents based thereon, and the use thereof
US5336755A (en) * 1992-01-28 1994-08-09 Belland Ag Process for the recovery of polymers dissolved in aqueous alkaline or acid media
US5340868A (en) * 1993-06-21 1994-08-23 Owens-Corning Fiberglass Technology Inc. Fibrous glass binders
US5387665A (en) * 1993-02-26 1995-02-07 Mitsui Toatsu Chemicals, Inc. Resins for electrohotographic toners
US5393849A (en) * 1993-10-19 1995-02-28 Georgia-Pacific Resins, Inc. Curable polyester/polyamino compositions
US5434233A (en) * 1992-08-12 1995-07-18 Kiely; Donald E. Polyaldaramide polymers useful for films and adhesives
US5480973A (en) * 1991-04-22 1996-01-02 Nadreph Limited Gel products and a process for making them
US5498662A (en) * 1993-10-20 1996-03-12 Kureha Kagaku Kogyo K.K. Gas barrier film and production process thereof
US5536766A (en) * 1994-03-15 1996-07-16 Basf Aktiengesellschaft Formaldehyde-free binding, impregnating or coating compositions for fibrous sheet materials
US5545279A (en) * 1992-12-30 1996-08-13 Hall; Herbert L. Method of making an insulation assembly
US5547541A (en) * 1992-08-17 1996-08-20 Weyerhaeuser Company Method for densifying fibers using a densifying agent
US5609727A (en) * 1992-08-17 1997-03-11 Weyerhaeuser Company Fibrous product for binding particles
US5620940A (en) * 1992-12-11 1997-04-15 United Technologies Corporation Process for forming a regenerable supported amine-polyol sorbent
US5633298A (en) * 1993-09-29 1997-05-27 W. R. Grace & Co.-Conn. Cement admixture product having improved rheological properties and process of forming same
US5645756A (en) * 1988-04-29 1997-07-08 Nalco Fuel Tech Hardness suppression in urea solutions
US5661213A (en) * 1992-08-06 1997-08-26 Rohm And Haas Company Curable aqueous composition and use as fiberglass nonwoven binder
US5756580A (en) * 1994-11-21 1998-05-26 Asahi Kasei Kogyo Kabushiki Kaisha Polymeric composite material
US5855987A (en) * 1993-02-15 1999-01-05 Bar Ilan University Bioactive conjugates of cellulose with amino compounds
US5885337A (en) * 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US5895804A (en) * 1997-10-27 1999-04-20 National Starch And Chemical Investment Holding Corporation Thermosetting polysaccharides
US5919831A (en) * 1995-05-01 1999-07-06 Philipp; Warren H. Process for making an ion exchange material
US5925722A (en) * 1995-03-24 1999-07-20 Giulini Chemie Gmbh Amphoteric and anionic polymer dispersions, process for their preparation and use thereof
US5929184A (en) * 1993-06-02 1999-07-27 Geltex Pharmaceuticals, Inc. Hydrophilic nonamine-containing and amine-containing copolymers and their use as bile acid sequestrants
US5932665A (en) * 1997-02-06 1999-08-03 Johns Manville International, Inc. Polycarboxy polymer acid binders having reduced cure temperatures
US5932344A (en) * 1995-02-07 1999-08-03 Daicel-Huels Ltd. Cement retarder and cement retardative sheet
US6072086A (en) * 1996-04-12 2000-06-06 Intergen Company Method and composition for controlling formaldehyde fixation by delayed quenching
US6077883A (en) * 1992-05-19 2000-06-20 Johns Manville International, Inc. Emulsified furan resin based glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US6090925A (en) * 1993-03-09 2000-07-18 Epic Therapeutics, Inc. Macromolecular microparticles and methods of production and use
US6171654B1 (en) * 1997-11-28 2001-01-09 Seydel Research, Inc. Method for bonding glass fibers with cross-linkable polyester resins
US6210472B1 (en) * 1999-04-08 2001-04-03 Marconi Data Systems Inc. Transparent coating for laser marking
US20020032253A1 (en) * 1997-02-05 2002-03-14 Juergen Lorenz Thermoplastic composite material
US6379739B1 (en) * 2000-09-20 2002-04-30 Griffith Laboratories Worldwide, Inc. Acidulant system for marinades
US6395856B1 (en) * 1998-04-17 2002-05-28 Crompton Corporation Silicone oligomers and curable compositions containing same
US20020091185A1 (en) * 1998-10-02 2002-07-11 Johns Manville International, Inc. Polycarboxy/polyol fiberglass binder
US20030005857A1 (en) * 1998-09-14 2003-01-09 Masato Minami Saccharide compound and a method of producing the same
US6525009B2 (en) * 2000-12-07 2003-02-25 International Business Machines Corporation Polycarboxylates-based aqueous compositions for cleaning of screening apparatus
US20040019168A1 (en) * 2002-07-26 2004-01-29 Soerens Dave Allen Absorbent binder composition and method of making it
US20040033747A1 (en) * 2002-08-16 2004-02-19 Miller Wayne P. Aqueous formaldehyde-free composition and fiberglass insulation including the same
US20040038017A1 (en) * 2002-06-18 2004-02-26 Georgia-Pacific Resins Corporation Polyester-type formaldehyde free insulation binder
US20040077055A1 (en) * 2001-02-16 2004-04-22 Cargill, Incorporated Glucosamine and method of making glucosamine from microbial biomass
US6753361B2 (en) * 2001-01-17 2004-06-22 Basf Aktiengesellschaft Compositions for producing moldings from finely divided materials
US20040122166A1 (en) * 2002-12-19 2004-06-24 O'brien-Bernini Frank C. Extended binder compositions
US6852247B2 (en) * 1999-07-26 2005-02-08 Archer-Daniels-Midland Company De-icing composition and method
US6858074B2 (en) * 2001-11-05 2005-02-22 Construction Research & Technology Gmbh High early-strength cementitious composition
US6861495B2 (en) * 2002-02-20 2005-03-01 E. I. Du Pont De Nemours And Company Lacquers containing highly branched copolyester polyol
US6864044B2 (en) * 2001-12-04 2005-03-08 Kanto Kagaku Kabushiki Kaisha Photoresist residue removing liquid composition
US20050059770A1 (en) * 2003-09-15 2005-03-17 Georgia-Pacific Resins Corporation Formaldehyde free insulation binder
US6884849B2 (en) * 2003-02-21 2005-04-26 Owens-Corning Fiberglas Technology, Inc. Poly alcohol-based binder composition
US7029717B1 (en) * 1999-04-16 2006-04-18 San-Ei Gen F.F.I., Inc. Sucralose-containing composition and edible products containing the composition
US20060099870A1 (en) * 2004-11-08 2006-05-11 Garcia Ruben G Fiber mat bound with a formaldehyde free binder, asphalt coated mat and method
US20060111480A1 (en) * 2002-07-15 2006-05-25 Hansen Erling L Formaldehyde-free aqueous binder composition for mineral fibers
US20060135433A1 (en) * 2002-10-08 2006-06-22 Murray Christopher J Phenolic binding peptides
US20070006390A1 (en) * 2005-07-06 2007-01-11 Guy Clamen Water repellant curable aqueous compositions
US20070009582A1 (en) * 2003-10-07 2007-01-11 Madsen Niels J Composition useful as an adhesive and use of such a composition
US7195792B2 (en) * 2002-02-22 2007-03-27 Genencor International, Inc. Browning agent
US7201778B2 (en) * 2003-01-13 2007-04-10 North Carolina State University Ionic cross-linking of ionic cotton with small molecular weight anionic or cationic molecules
US20080108741A1 (en) * 2006-11-03 2008-05-08 Dynea Oy Renewable binder for nonwoven materials
US20100098947A1 (en) * 2005-08-26 2010-04-22 Asahi Fiber Glass Company, Limited Aqueous binder for inorganic fiber and thermal and/or acoustical insulation material using the same
US20100175826A1 (en) * 2005-06-24 2010-07-15 Saint-Gobain Isover Method for producing bonded mineral wool and binder therefor

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1886353A (en) * 1922-04-27 1932-11-01 John Stogdell Stokes Synthetic resin and method of making same
BE471265A (en) * 1942-04-02
US3856606A (en) * 1968-06-17 1974-12-24 Union Carbide Corp Coupling solid substrates using silyl peroxide compounds
SU374400A1 (en) 1970-07-09 1973-03-20 METHOD OF OBTAINING NONWAVE MATERIALS
IT971367B (en) * 1972-11-30 1974-04-30 Sir Soc Italiana Resine Spa PROCEDURE FOR THE CONTINUOUS PREPARATION OF UNSATURATED POLYESTERS
US4054713A (en) 1973-12-28 1977-10-18 Kao Soap Co., Ltd. Process for preparing glass fiber mats
US4048127A (en) 1976-07-22 1977-09-13 Cpc International Inc. Carbohydrate-based condensation resin
DE2721186C2 (en) 1977-05-11 1986-04-24 Bayer Ag, 5090 Leverkusen Process for the preparation of a mixture of low molecular weight polyhydroxyl compounds
US4233432A (en) 1979-05-10 1980-11-11 United States Steel Corporation Dicyclopentadiene polyester resins
US4296173A (en) 1979-09-13 1981-10-20 Ppg Industries, Inc. Glass fibers with reduced tendency to form gumming deposits and sizing composition comprising two starches with different amylose content
GB2078805A (en) 1980-06-27 1982-01-13 Tba Industrial Products Ltd Fire and Weld Splash Resistant for Glass Fabric
US4357194A (en) 1981-04-14 1982-11-02 John Stofko Steam bonding of solid lignocellulosic material
US4692478A (en) 1986-03-14 1987-09-08 Chemical Process Corporation Process for preparation of resin and resin obtained
GB8809486D0 (en) 1987-04-22 1988-05-25 Micropore International Ltd Procedure to manufacture thermal insulating material for use at high temperatures
FR2638448B1 (en) 1988-10-27 1992-08-21 Saint Gobain Isover BINDER AND BONDING THEREOF FOR MINERAL FIBERS
US5582682A (en) 1988-12-28 1996-12-10 Ferretti; Arthur Process and a composition for making cellulosic composites
US5371194A (en) 1988-12-28 1994-12-06 Ferretti; Arthur Biomass derived thermosetting resin
US5151465A (en) 1990-01-04 1992-09-29 Arco Chemical Technology, L.P. Polymer compositions and absorbent fibers produced therefrom
US6495656B1 (en) 1990-11-30 2002-12-17 Eastman Chemical Company Copolyesters and fibrous materials formed therefrom
EP0492016B1 (en) 1990-12-28 2002-09-18 K.C. Shen Technology International Ltd. Thermosetting resin material and composite products from lignocellulose
DE4127733A1 (en) 1991-08-22 1993-02-25 Basf Ag Graft polymers of natural substances containing saccharide structures or derivatives thereof and ethylenically unsaturated compounds and their use.
GB9126828D0 (en) 1991-12-18 1992-02-19 British American Tobacco Co Improvements relating to smoking articles
ES2182830T3 (en) 1992-08-17 2003-03-16 Weyerhaeuser Co METHOD OF UNION OF PARTICLES TO FIBERS.
US5352480A (en) 1992-08-17 1994-10-04 Weyerhaeuser Company Method for binding particles to fibers using reactivatable binders
FR2694894B1 (en) 1992-08-20 1994-11-10 Coletica Use of a transacylation reaction between an esterified polysaccharide and a polyamine or polyhydroxylated substance for the manufacture of microparticles, process and composition.
US5981719A (en) 1993-03-09 1999-11-09 Epic Therapeutics, Inc. Macromolecular microparticles and methods of production and use
US5955448A (en) 1994-08-19 1999-09-21 Quadrant Holdings Cambridge Limited Method for stabilization of biological substances during drying and subsequent storage and compositions thereof
GB9411080D0 (en) 1994-06-02 1994-07-20 Unilever Plc Treatment
CA2161592A1 (en) 1994-11-03 1996-05-04 David P. Aschenbeck Method for manufacturing mineral fibers
US5720796A (en) 1995-08-08 1998-02-24 W. R. Grace & Co.-Conn. Process of using roll press grinding aid for granulated blast furnace slag
US5942123A (en) 1995-09-05 1999-08-24 Mcardle; Blaise Method of using a filter aid protein-polysaccharide complex composition
US6319683B1 (en) 1996-04-12 2001-11-20 Intergen Company Method and composition for controlling formaldehyde fixation by delayed quenching
DE19621573A1 (en) 1996-05-29 1997-12-04 Basf Ag Thermally curable, aqueous compositions
AU742125B2 (en) 1996-08-21 2001-12-20 Rohm And Haas Company A formaldehyde-free, accelerated cure aqueous composition for bonding glass fiber-heat resistant nonwovens
US6067821A (en) * 1996-10-07 2000-05-30 Owens Corning Fiberglas Technology, Inc. Process for making mineral wool fibers from lumps of uncalcined raw bauxite
NL1004379C2 (en) 1996-10-29 1998-05-08 Borculo Cooep Weiprod Use of sugar amines and sugar amides as an adhesive, as well as new sugar amines and sugar amides.
US20020161108A1 (en) 2000-03-09 2002-10-31 Stepan Company, A Corporation Of The State Of Delaware Emulsion polymerization process utilizing ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids
US6310227B1 (en) 1997-01-31 2001-10-30 The Procter & Gamble Co. Reduced calorie cooking and frying oils having improved hydrolytic stability, and process for preparing
CN1089727C (en) 1997-04-11 2002-08-28 广州市环境保护科学研究所 Method for preparing cation/amphoteric graft polyacrylamide flocculating agent
TW408152B (en) 1997-04-25 2000-10-11 Rohm & Haas Formaldehyde-free curable composition and method for bonding heat-resistant fibers of a nonwoven material by using the composition
US5977232A (en) 1997-08-01 1999-11-02 Rohm And Haas Company Formaldehyde-free, accelerated cure, aqueous composition for bonding glass fiber heat-resistant nonwovens
US5983586A (en) * 1997-11-24 1999-11-16 Owens Corning Fiberglas Technology, Inc. Fibrous insulation having integrated mineral fibers and organic fibers, and building structures insulated with such fibrous insulation
JP3907837B2 (en) 1998-06-12 2007-04-18 富士フイルム株式会社 Image recording material
US6331350B1 (en) 1998-10-02 2001-12-18 Johns Manville International, Inc. Polycarboxy/polyol fiberglass binder of low pH
US6231721B1 (en) 1998-10-09 2001-05-15 Weyerhaeuser Company Compressible wood pulp product
DE60039084D1 (en) 1999-03-19 2008-07-17 Saint Gobain Cultilene B V Substrate for ungodly culture
WO2000058085A1 (en) 1999-03-31 2000-10-05 Penford Corporation Packaging and structural materials comprising potato peel waste
EP1170265A1 (en) 2000-07-04 2002-01-09 Rockwool International A/S Binder for mineral wool products
AU782086B2 (en) 2000-09-20 2005-06-30 Akzo Nobel N.V. Mono(hydroxyalkyl) urea and polysaccharide crosslinking systems
US7157524B2 (en) 2001-05-31 2007-01-02 Owens Corning Fiberglas Technology, Inc. Surfactant-containing insulation binder
TWI320039B (en) 2001-09-21 2010-02-01 Lactam-containing compounds and derivatives thereof as factor xa inhibitors
US6955844B2 (en) 2002-05-24 2005-10-18 Innovative Construction And Building Materials Construction materials containing surface modified fibers
FR2842189B1 (en) 2002-07-12 2005-03-04 Saint Gobain Isover THERMALLY INSULATING PRODUCT AND MANUFACTURING METHOD THEREOF
US7090745B2 (en) 2002-09-13 2006-08-15 University Of Pittsburgh Method for increasing the strength of a cellulosic product
US7141626B2 (en) 2002-10-29 2006-11-28 National Starch And Chemical Investment Holding Corporation Fiberglass non-woven catalyst
US7947766B2 (en) 2003-06-06 2011-05-24 The Procter & Gamble Company Crosslinking systems for hydroxyl polymers
US20040254285A1 (en) 2003-06-12 2004-12-16 Rodrigues Klein A. Fiberglass nonwoven binder
BRPI0414847B1 (en) 2003-10-06 2016-04-12 Saint Gobain Isover insulation material element
EP1522642A1 (en) * 2003-10-06 2005-04-13 Saint-Gobain Isover G+H Ag Insulating mat of mineral fibre wound in a roll for press fitting between beams
FR2861721B1 (en) 2003-11-05 2006-01-27 Saint Gobain Isover SIZING COMPOSITION FOR INSULATING PRODUCTS BASED ON MINERAL WOOL AND RESULTING PRODUCTS
US20050208095A1 (en) 2003-11-20 2005-09-22 Angiotech International Ag Polymer compositions and methods for their use
US20050215153A1 (en) 2004-03-23 2005-09-29 Cossement Marc R Dextrin binder composition for heat resistant non-wovens
JP4351109B2 (en) 2004-04-12 2009-10-28 旭ファイバーグラス株式会社 Inorganic fiber mat
US6977116B2 (en) 2004-04-29 2005-12-20 The Procter & Gamble Company Polymeric structures and method for making same
US8603631B2 (en) 2004-10-13 2013-12-10 Knauf Insulation Gmbh Polyester binding compositions
US7514027B2 (en) 2005-02-17 2009-04-07 Saint-Gobain Isover Process for manufacturing products of mineral wool, in particular monolayer and multilayer products
KR100712970B1 (en) 2005-03-03 2007-05-02 롬 앤드 하아스 컴패니 Method for reducing corrosion
SI1885785T1 (en) 2005-05-06 2014-12-31 Dynea Chemicals Oy Poly (vinyl alcohol) - based formaldehyde-free curable aqueous composition
SI2574640T1 (en) * 2005-07-26 2023-05-31 Knauf Insulation Gmbh Binders and materials made therewith
SI2826903T1 (en) 2007-01-25 2023-10-30 Knauf Insulation Method of manufacturing mineral fiber insulation product
US20100084598A1 (en) * 2007-01-25 2010-04-08 Roger Jackson Mineral fibre insulation
DK2108006T3 (en) * 2007-01-25 2020-12-21 Knauf Insulation Gmbh BINDERS AND MATERIALS MADE THEREFORE
GB0715100D0 (en) 2007-08-03 2007-09-12 Knauf Insulation Ltd Binders

Patent Citations (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1801052A (en) * 1923-02-06 1931-04-14 Meigsoid Corp Resinous condensation product and process of making same
US1801053A (en) * 1925-01-22 1931-04-14 Meigsoid Corp Carbohydrate product and process of making same
US2393105A (en) * 1943-05-22 1946-01-15 Cook Electric Co Adapter
US3232821A (en) * 1964-12-11 1966-02-01 Ferro Corp Felted fibrous mat and apparatus for manufacturing same
US3826767A (en) * 1972-01-26 1974-07-30 Calgon Corp Anionic dextran graft copolymers
US3802897A (en) * 1973-02-23 1974-04-09 Anheuser Busch Water resistant starch adhesive
US3809664A (en) * 1973-08-16 1974-05-07 Us Agriculture Method of preparing starch graft polymers
US4107379A (en) * 1974-02-22 1978-08-15 John Stofko Bonding of solid lignocellulosic material
US4183997A (en) * 1974-02-22 1980-01-15 John Jansky Bonding of solid lignocellulosic material
US4028290A (en) * 1975-10-23 1977-06-07 Hercules Incorporated Highly absorbent modified polysaccharides
US4148765A (en) * 1977-01-10 1979-04-10 The Dow Chemical Company Polyester resins containing dicyclopentadiene
US4097427A (en) * 1977-02-14 1978-06-27 Nalco Chemical Company Cationization of starch utilizing alkali metal hydroxide, cationic water-soluble polymer and oxidant for improved wet end strength
US4322523A (en) * 1978-07-28 1982-03-30 Bayer Aktiengesellschaft Methylolated mono- and oligosaccharides
US4246367A (en) * 1979-09-24 1981-01-20 United States Steel Corporation Dicyclopentadiene polyester resins
US4278573A (en) * 1980-04-07 1981-07-14 National Starch And Chemical Corporation Preparation of cationic starch graft copolymers from starch, N,N-methylenebisacrylamide, and polyamines
US4330443A (en) * 1980-06-18 1982-05-18 The United States Of America As Represented By The Secretary Of Agriculture Dry chemical process for grafting acrylic and methyl acrylic ester and amide monomers onto starch-containing materials
US4400496A (en) * 1980-09-22 1983-08-23 University Of Florida Water-soluble graft copolymers of starch-acrylamide and uses therefor
US4464523A (en) * 1983-05-16 1984-08-07 National Starch And Chemical Corporation Process for the preparation of graft copolymers of cellulose derivatives and diallyl, dialkyl ammonium halides
US4668716A (en) * 1983-09-30 1987-05-26 Union Carbide Corporation Novel fatty ethenoid acylaminoorganosilicon compounds and their use as a coupling agent
US4524164A (en) * 1983-12-02 1985-06-18 Chemical Process Corporation Thermosetting adhesive resins
US4754056A (en) * 1985-04-05 1988-06-28 Desoto, Inc. Radiation-curable coatings containing reactive pigment dispersants
US4906237A (en) * 1985-09-13 1990-03-06 Astra Meditec Ab Method of forming an improved hydrophilic coating on a polymer surface
US5336753A (en) * 1986-08-29 1994-08-09 Basf Lacke + Farben Ag Polycondensation and/or addition product containing carboxyl groups and tertiary amino groups, coating agents based thereon, and the use thereof
US5106615A (en) * 1986-10-14 1992-04-21 Shabtay Dikstein Eyedrops having non-newtonian rheological properties
US4845162A (en) * 1987-06-01 1989-07-04 Allied-Signal Inc. Curable phenolic and polyamide blends
US4912147A (en) * 1987-10-14 1990-03-27 Basf Aktiengesellschaft Preparation of aqueous (meth)acrylate copolymer dispersions in two stages and their use as impregnating materials, coating materials and binders for sheet-like fibrous structures
US4923980A (en) * 1987-11-10 1990-05-08 Biocarb Ab Process for the manufacture of a gel product
US5095054A (en) * 1988-02-03 1992-03-10 Warner-Lambert Company Polymer compositions containing destructurized starch
US5645756A (en) * 1988-04-29 1997-07-08 Nalco Fuel Tech Hardness suppression in urea solutions
US5037930A (en) * 1989-09-22 1991-08-06 Gaf Chemicals Corporation Heterocyclic quaternized nitrogen-containing cellulosic graft polymers
US5124369A (en) * 1989-11-08 1992-06-23 Shell Oil Company Process for preparing soft flexible polyurethane foams and a polyol composition useful in said process
US5114004A (en) * 1990-02-14 1992-05-19 Material Engineering Technology Laboratory Inc. Filled and sealed, self-contained mixing container
US5041595A (en) * 1990-09-26 1991-08-20 Union Carbide Chemicals And Plastics Technology Corporation Method for manufacturing vinylalkoxysilanes
US5480973A (en) * 1991-04-22 1996-01-02 Nadreph Limited Gel products and a process for making them
US5128407A (en) * 1991-07-25 1992-07-07 Miles Inc. Urea extended polyisocyanates
US5336755A (en) * 1992-01-28 1994-08-09 Belland Ag Process for the recovery of polymers dissolved in aqueous alkaline or acid media
US6077883A (en) * 1992-05-19 2000-06-20 Johns Manville International, Inc. Emulsified furan resin based glass fiber binding compositions, process of binding glass fibers, and glass fiber compositions
US5661213A (en) * 1992-08-06 1997-08-26 Rohm And Haas Company Curable aqueous composition and use as fiberglass nonwoven binder
US6221973B1 (en) * 1992-08-06 2001-04-24 Rohm And Haas Company Curable aqueous composition and use as fiberglass nonwoven binder
US5763524A (en) * 1992-08-06 1998-06-09 Arkens; Charles Thomas Curable aqueous composition and use as fiberglass non woven binder
US5434233A (en) * 1992-08-12 1995-07-18 Kiely; Donald E. Polyaldaramide polymers useful for films and adhesives
US5609727A (en) * 1992-08-17 1997-03-11 Weyerhaeuser Company Fibrous product for binding particles
US5308896A (en) * 1992-08-17 1994-05-03 Weyerhaeuser Company Particle binders for high bulk fibers
US5614570A (en) * 1992-08-17 1997-03-25 Weyerhaeuser Company Absorbent articles containing binder carrying high bulk fibers
US5547541A (en) * 1992-08-17 1996-08-20 Weyerhaeuser Company Method for densifying fibers using a densifying agent
US5620940A (en) * 1992-12-11 1997-04-15 United Technologies Corporation Process for forming a regenerable supported amine-polyol sorbent
US5545279A (en) * 1992-12-30 1996-08-13 Hall; Herbert L. Method of making an insulation assembly
US5855987A (en) * 1993-02-15 1999-01-05 Bar Ilan University Bioactive conjugates of cellulose with amino compounds
US5387665A (en) * 1993-02-26 1995-02-07 Mitsui Toatsu Chemicals, Inc. Resins for electrohotographic toners
US6090925A (en) * 1993-03-09 2000-07-18 Epic Therapeutics, Inc. Macromolecular microparticles and methods of production and use
US5929184A (en) * 1993-06-02 1999-07-27 Geltex Pharmaceuticals, Inc. Hydrophilic nonamine-containing and amine-containing copolymers and their use as bile acid sequestrants
US5340868A (en) * 1993-06-21 1994-08-23 Owens-Corning Fiberglass Technology Inc. Fibrous glass binders
US5318990A (en) * 1993-06-21 1994-06-07 Owens-Corning Fiberglas Technology Inc. Fibrous glass binders
US5633298A (en) * 1993-09-29 1997-05-27 W. R. Grace & Co.-Conn. Cement admixture product having improved rheological properties and process of forming same
US5643978A (en) * 1993-09-29 1997-07-01 W. R. Grace & Co.-Conn. Cement admixture product having improved rheological properties and process of forming same
US5393849A (en) * 1993-10-19 1995-02-28 Georgia-Pacific Resins, Inc. Curable polyester/polyamino compositions
US5498662A (en) * 1993-10-20 1996-03-12 Kureha Kagaku Kogyo K.K. Gas barrier film and production process thereof
US5621026A (en) * 1993-10-20 1997-04-15 Kureha Kagaku Kogyo K.K. Gas barrier film and production process thereof
US5536766A (en) * 1994-03-15 1996-07-16 Basf Aktiengesellschaft Formaldehyde-free binding, impregnating or coating compositions for fibrous sheet materials
US5756580A (en) * 1994-11-21 1998-05-26 Asahi Kasei Kogyo Kabushiki Kaisha Polymeric composite material
US5932344A (en) * 1995-02-07 1999-08-03 Daicel-Huels Ltd. Cement retarder and cement retardative sheet
US5925722A (en) * 1995-03-24 1999-07-20 Giulini Chemie Gmbh Amphoteric and anionic polymer dispersions, process for their preparation and use thereof
US5919831A (en) * 1995-05-01 1999-07-06 Philipp; Warren H. Process for making an ion exchange material
US5885337A (en) * 1995-11-28 1999-03-23 Nohr; Ronald Sinclair Colorant stabilizers
US6072086A (en) * 1996-04-12 2000-06-06 Intergen Company Method and composition for controlling formaldehyde fixation by delayed quenching
US20020032253A1 (en) * 1997-02-05 2002-03-14 Juergen Lorenz Thermoplastic composite material
US5932665A (en) * 1997-02-06 1999-08-03 Johns Manville International, Inc. Polycarboxy polymer acid binders having reduced cure temperatures
US5895804A (en) * 1997-10-27 1999-04-20 National Starch And Chemical Investment Holding Corporation Thermosetting polysaccharides
US6171654B1 (en) * 1997-11-28 2001-01-09 Seydel Research, Inc. Method for bonding glass fibers with cross-linkable polyester resins
US6395856B1 (en) * 1998-04-17 2002-05-28 Crompton Corporation Silicone oligomers and curable compositions containing same
US20030005857A1 (en) * 1998-09-14 2003-01-09 Masato Minami Saccharide compound and a method of producing the same
US7067579B2 (en) * 1998-10-02 2006-06-27 Johns Manville Polycarboxy/polyol fiberglass binder
US20020091185A1 (en) * 1998-10-02 2002-07-11 Johns Manville International, Inc. Polycarboxy/polyol fiberglass binder
US6210472B1 (en) * 1999-04-08 2001-04-03 Marconi Data Systems Inc. Transparent coating for laser marking
US7029717B1 (en) * 1999-04-16 2006-04-18 San-Ei Gen F.F.I., Inc. Sucralose-containing composition and edible products containing the composition
US6852247B2 (en) * 1999-07-26 2005-02-08 Archer-Daniels-Midland Company De-icing composition and method
US6379739B1 (en) * 2000-09-20 2002-04-30 Griffith Laboratories Worldwide, Inc. Acidulant system for marinades
US6525009B2 (en) * 2000-12-07 2003-02-25 International Business Machines Corporation Polycarboxylates-based aqueous compositions for cleaning of screening apparatus
US6753361B2 (en) * 2001-01-17 2004-06-22 Basf Aktiengesellschaft Compositions for producing moldings from finely divided materials
US20040077055A1 (en) * 2001-02-16 2004-04-22 Cargill, Incorporated Glucosamine and method of making glucosamine from microbial biomass
US6858074B2 (en) * 2001-11-05 2005-02-22 Construction Research & Technology Gmbh High early-strength cementitious composition
US6864044B2 (en) * 2001-12-04 2005-03-08 Kanto Kagaku Kabushiki Kaisha Photoresist residue removing liquid composition
US6861495B2 (en) * 2002-02-20 2005-03-01 E. I. Du Pont De Nemours And Company Lacquers containing highly branched copolyester polyol
US7195792B2 (en) * 2002-02-22 2007-03-27 Genencor International, Inc. Browning agent
US20040038017A1 (en) * 2002-06-18 2004-02-26 Georgia-Pacific Resins Corporation Polyester-type formaldehyde free insulation binder
US20060111480A1 (en) * 2002-07-15 2006-05-25 Hansen Erling L Formaldehyde-free aqueous binder composition for mineral fibers
US20040019168A1 (en) * 2002-07-26 2004-01-29 Soerens Dave Allen Absorbent binder composition and method of making it
US20040033747A1 (en) * 2002-08-16 2004-02-19 Miller Wayne P. Aqueous formaldehyde-free composition and fiberglass insulation including the same
US20060135433A1 (en) * 2002-10-08 2006-06-22 Murray Christopher J Phenolic binding peptides
US20040122166A1 (en) * 2002-12-19 2004-06-24 O'brien-Bernini Frank C. Extended binder compositions
US7201778B2 (en) * 2003-01-13 2007-04-10 North Carolina State University Ionic cross-linking of ionic cotton with small molecular weight anionic or cationic molecules
US6884849B2 (en) * 2003-02-21 2005-04-26 Owens-Corning Fiberglas Technology, Inc. Poly alcohol-based binder composition
US20050059770A1 (en) * 2003-09-15 2005-03-17 Georgia-Pacific Resins Corporation Formaldehyde free insulation binder
US20070009582A1 (en) * 2003-10-07 2007-01-11 Madsen Niels J Composition useful as an adhesive and use of such a composition
US20060099870A1 (en) * 2004-11-08 2006-05-11 Garcia Ruben G Fiber mat bound with a formaldehyde free binder, asphalt coated mat and method
US20100175826A1 (en) * 2005-06-24 2010-07-15 Saint-Gobain Isover Method for producing bonded mineral wool and binder therefor
US20070006390A1 (en) * 2005-07-06 2007-01-11 Guy Clamen Water repellant curable aqueous compositions
US20100098947A1 (en) * 2005-08-26 2010-04-22 Asahi Fiber Glass Company, Limited Aqueous binder for inorganic fiber and thermal and/or acoustical insulation material using the same
US20080108741A1 (en) * 2006-11-03 2008-05-08 Dynea Oy Renewable binder for nonwoven materials

Cited By (53)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110054143A1 (en) * 2004-03-11 2011-03-03 Helbing Clarence H Binder compositions and associated methods
US8691934B2 (en) 2004-03-11 2014-04-08 Knauf Insulation Gmbh Binder compositions and associated methods
US20100092785A1 (en) * 2004-10-13 2010-04-15 Helbing Clarence H Polyester binding compositions
US8603631B2 (en) * 2004-10-13 2013-12-10 Knauf Insulation Gmbh Polyester binding compositions
US9040652B2 (en) 2005-07-26 2015-05-26 Knauf Insulation, Llc Binders and materials made therewith
US9260627B2 (en) 2005-07-26 2016-02-16 Knauf Insulation, Inc. Binders and materials made therewith
US9926464B2 (en) 2005-07-26 2018-03-27 Knauf Insulation, Inc. Binders and materials made therewith
US9745489B2 (en) 2005-07-26 2017-08-29 Knauf Insulation, Inc. Binders and materials made therewith
US9464207B2 (en) 2005-07-26 2016-10-11 Knauf Insulation, Inc. Binders and materials made therewith
US9434854B2 (en) 2005-07-26 2016-09-06 Knauf Insulation, Inc. Binders and materials made therewith
US11905206B2 (en) 2007-01-25 2024-02-20 Knauf Insulation, Inc. Binders and materials made therewith
US8901208B2 (en) 2007-01-25 2014-12-02 Knauf Insulation Sprl Composite wood board
US10759695B2 (en) 2007-01-25 2020-09-01 Knauf Insulation, Inc. Binders and materials made therewith
US11401209B2 (en) 2007-01-25 2022-08-02 Knauf Insulation, Inc. Binders and materials made therewith
US9447281B2 (en) 2007-01-25 2016-09-20 Knauf Insulation Sprl Composite wood board
US11459754B2 (en) 2007-01-25 2022-10-04 Knauf Insulation, Inc. Mineral fibre board
US10000639B2 (en) 2007-01-25 2018-06-19 Knauf Insulation Sprl Composite wood board
US9828287B2 (en) 2007-01-25 2017-11-28 Knauf Insulation, Inc. Binders and materials made therewith
US10968629B2 (en) 2007-01-25 2021-04-06 Knauf Insulation, Inc. Mineral fibre board
US11453780B2 (en) 2007-01-25 2022-09-27 Knauf Insulation, Inc. Composite wood board
US9309436B2 (en) 2007-04-13 2016-04-12 Knauf Insulation, Inc. Composite maillard-resole binders
US11946582B2 (en) 2007-08-03 2024-04-02 Knauf Insulation, Inc. Binders
US9469747B2 (en) 2007-08-03 2016-10-18 Knauf Insulation Sprl Mineral wool insulation
US8940089B2 (en) 2007-08-03 2015-01-27 Knauf Insulation Sprl Binders
US9039827B2 (en) 2007-08-03 2015-05-26 Knauf Insulation, Llc Binders
US10053558B2 (en) 2009-08-07 2018-08-21 Knauf Insulation, Inc. Molasses binder
US9416248B2 (en) 2009-08-07 2016-08-16 Knauf Insulation, Inc. Molasses binder
US8900495B2 (en) 2009-08-07 2014-12-02 Knauf Insulation Molasses binder
US9493603B2 (en) 2010-05-07 2016-11-15 Knauf Insulation Sprl Carbohydrate binders and materials made therewith
US10738160B2 (en) 2010-05-07 2020-08-11 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US11814481B2 (en) 2010-05-07 2023-11-14 Knauf Insulation, Inc. Carbohydrate polyamine binders and materials made therewith
US9505883B2 (en) 2010-05-07 2016-11-29 Knauf Insulation Sprl Carbohydrate polyamine binders and materials made therewith
US10913760B2 (en) 2010-05-07 2021-02-09 Knauf Insulation, Inc. Carbohydrate binders and materials made therewith
US11078332B2 (en) 2010-05-07 2021-08-03 Knauf Insulation, Inc. Carbohydrate polyamine binders and materials made therewith
US11846097B2 (en) 2010-06-07 2023-12-19 Knauf Insulation, Inc. Fiber products having temperature control additives
US10767050B2 (en) 2011-05-07 2020-09-08 Knauf Insulation, Inc. Liquid high solids binder composition
US10287462B2 (en) * 2012-04-05 2019-05-14 Knauf Insulation, Inc. Binders and associated products
US11453807B2 (en) 2012-04-05 2022-09-27 Knauf Insulation, Inc. Binders and associated products
US20150053114A1 (en) * 2012-04-05 2015-02-26 Knauf Insulation Binders and associated products
US20160280971A1 (en) * 2012-04-05 2016-09-29 Knauf Insulation Sprl Binders and associated products
US11725124B2 (en) 2012-04-05 2023-08-15 Knauf Insulation, Inc. Binders and associated products
US9492943B2 (en) 2012-08-17 2016-11-15 Knauf Insulation Sprl Wood board and process for its production
US10183416B2 (en) 2012-08-17 2019-01-22 Knauf Insulation, Inc. Wood board and process for its production
US10508172B2 (en) 2012-12-05 2019-12-17 Knauf Insulation, Inc. Binder
US11384203B2 (en) 2012-12-05 2022-07-12 Knauf Insulation, Inc. Binder
US11401204B2 (en) 2014-02-07 2022-08-02 Knauf Insulation, Inc. Uncured articles with improved shelf-life
US11332577B2 (en) 2014-05-20 2022-05-17 Knauf Insulation Sprl Binders
US10864653B2 (en) 2015-10-09 2020-12-15 Knauf Insulation Sprl Wood particle boards
US11230031B2 (en) 2015-10-09 2022-01-25 Knauf Insulation Sprl Wood particle boards
US11060276B2 (en) 2016-06-09 2021-07-13 Knauf Insulation Sprl Binders
US11248108B2 (en) 2017-01-31 2022-02-15 Knauf Insulation Sprl Binder compositions and uses thereof
US11939460B2 (en) 2018-03-27 2024-03-26 Knauf Insulation, Inc. Binder compositions and uses thereof
US11945979B2 (en) 2018-03-27 2024-04-02 Knauf Insulation, Inc. Composite products

Also Published As

Publication number Publication date
US7854980B2 (en) 2010-12-21
DK2826903T3 (en) 2023-06-06
ES2526345T3 (en) 2015-01-09
CN101688343A (en) 2010-03-31
SI2126179T1 (en) 2014-12-31
PL2126179T3 (en) 2015-02-27
US20100080976A1 (en) 2010-04-01
EP2126179B1 (en) 2014-10-22
SI2826903T1 (en) 2023-10-30
EP2826903A1 (en) 2015-01-21
PL2826903T3 (en) 2023-07-24
ES2945888T3 (en) 2023-07-10
PT2126179E (en) 2014-12-29
EP2126179A1 (en) 2009-12-02
EP2826903B8 (en) 2023-06-07
DK2126179T3 (en) 2014-11-03
BRPI0721233A2 (en) 2013-01-01
WO2008089851A1 (en) 2008-07-31
CN101688343B (en) 2011-12-14
EP2826903B1 (en) 2023-04-26

Similar Documents

Publication Publication Date Title
US7854980B2 (en) Formaldehyde-free mineral fibre insulation product
US11459754B2 (en) Mineral fibre board
EP4012087B1 (en) Binder system
JP2023504432A (en) fiberglass insulation products
KR20190030708A (en) insulator
JP2023504433A (en) fiberglass insulation products
JP2024508589A (en) insulation products
DE202007019653U1 (en) Formaldehyde-free insulating product of mineral fibers

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: EXPRESSLY ABANDONED -- DURING EXAMINATION