WO2006023137A2 - Control of pre-cured product moisture for formaldehyde-free fiberglass products - Google Patents
Control of pre-cured product moisture for formaldehyde-free fiberglass products Download PDFInfo
- Publication number
- WO2006023137A2 WO2006023137A2 PCT/US2005/024025 US2005024025W WO2006023137A2 WO 2006023137 A2 WO2006023137 A2 WO 2006023137A2 US 2005024025 W US2005024025 W US 2005024025W WO 2006023137 A2 WO2006023137 A2 WO 2006023137A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- moisture
- fibers
- binder
- moisture content
- formaldehyde
- Prior art date
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Classifications
-
- 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
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
-
- 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
- C03C25/24—Coatings containing organic materials
- C03C25/26—Macromolecular compounds or prepolymers
- C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
- C03C25/323—Polyesters, e.g. alkyd resins
Definitions
- the present invention relates to a method for controlling the pre-cured moisture in glass fibers coated with novel, formaldehyde-free binders. Controlling the moisture content of the pre-cured products ensures proper curing of the binder composition. Control is achieved.
- Fiberglass binders have a variety of uses ranging from stiffening applications where the binder is applied to woven or non-woven fiberglass sheet goods and cured, producing a stiffer product; thermo-forming applications wherein the binder resin is applied to sheet or lofty fibrous product following which it is dried and optionally B-staged to form an intermediate but yet curable product; and to fully cured systems such as building insulation.
- Fibrous glass insulation products generally comprise matted glass fibers bonded together by a cured thermoset polymeric material. Molten streams of glass are drawn into fibers of random lengths and blown into a forming chamber where they are randomly deposited as a mat onto a traveling conveyor. The fibers, while in transit in the forming chamber and while still hot from the drawing operation, are sprayed with an aqueous binder.
- a phenol-formaldehyde binder is currently used throughout the fibrous glass insulation industry.
- the residual heat from the glass fibers and the flow of air through the fibrous mat during the forming operation are generally sufficient to volatilize the majority to all of the water from the binder, thereby leaving the remaining components of the binder on the fibers as a viscous or semi-viscous high solids liquid.
- the coated fibrous mat is transferred to a curing oven where heated air, for example, is blown through the mat to cure the binder and rigidly bond the glass fibers together.
- Fiberglass binders used in the present sense should not be confused with matrix resins which are an entirely different and non-analogous field of art. While sometimes termed “binders", matrix resins act to fill the entire interstitial space between fibers, resulting in a dense, fiber reinforced product where the matrix must translate the fiber strength properties to the composite, whereas "binder resins" as used herein are not space-filling, but rather coat only the fibers, and particularly the junctions of fibers. Fiberglass binders also cannot be equated with paper or wood product "binders” where the adhesive properties are tailored to the chemical nature of the cellulosic substrates. Many such resins, e.g. resorcinol/formaldehyde resins, are not suitable for use as fiberglass binders. One skilled in the art of fiberglass binders would not look to cellulosic binders to solve any of the known problems associated with fiberglass binders.
- Binders useful in fiberglass insulation products generally require a low viscosity in the uncured state, yet characteristics so as to form a rigid thermoset polymeric mat for the glass fibers when cured.
- a low binder viscosity in the uncured state is required to allow the mat to be sized correctly.
- viscous binders tend to be tacky or sticky and hence they lead to accumulation of fiber on the forming chamber walls. This accumulated fiber may later fall onto the mat causing dense areas and product problems.
- a binder which forms a rigid matrix when cured is required so that a finished fiberglass thermal insulation product, when compressed for packaging and shipping, will recover to its specified vertical dimension when installed in a building.
- thermosetting fiber-glass binder resins From among the many thermosetting polymers, numerous candidates for suitable thermosetting fiber-glass binder resins exist. However, binder-coated fiberglass products are often of the commodity type, and thus cost becomes a driving factor, generally ruling out such resins as thermosetting polyurethanes, epoxies, and others. Due to their excellent cost/performance ratio, the resins of choice in the past have been phenol/formaldehyde resins. Phenol/formaldehyde resins can be economically produced, and can be extended with urea prior to use as a binder in many applications. Such urea- extended phenol/formaldehyde binders have been the mainstay of the fiberglass insulation industry for years.
- VOCs volatile organic compound emissions
- One particularly useful formaldehyde-free binder system employs a binder comprising a polycarboxy polymer and a polyol.
- Formaldehyde-free resins are those which are not made with formaldehyde or formaldehyde-generating compounds. Formaldehyde-free resins do not emit appreciable levels of formaldehyde during the insulation manufacturing process and do not emit formaldehyde under normal service conditions.
- the binder compositions result in final products which have properties equal to or superior to those made with traditional binders, the compositions also present technical challenges.
- One such challenge is controlling the moisture of the product as it enters the curing oven. It has been found that if the residual moisture of the product entering into the curing oven exceeds 20 percent by weight of the product, uneven curing results which can detrimentally affect the performance of the product.
- Control of residual moisture in pre-cured fiberglass products using a formaldehyde-free binder is achieved by monitoring the residual moisture before the product enters the curing oven; comparing the measured residual moisture to a pre ⁇ determined value and, if the measured moisture exceeds the pre-set values, adjusting one or more upstream process conditions to reduce the residual water content in the pre- cured product.
- Moisture content can be measured by a number of known techniques.
- radiofrequency e.g., microwave
- near infrared near infrared
- the moisture values can range from 0 to over 20% weight percent (wt%) with at least about 4 weight percent (wt%) preferred.
- the process conditions which can be adjusted are any condition which affects the residual moisture in the pre-cured product.
- the conditions that can affect residual moisture include the amount of process water added to the binder resin to form the binder composition; heating the binder coated glass fibers in the collection box; and the flow of air through the fibers in the collector box.
- Other process conditions that can be adjusted are well-known to those skilled in the art.
- FIG. 1 is a schematic of the moisture control system of the invention. DETAILED DESCRIPTION OF THE INVENTION
- Fiberglass products having a formaldehyde-free binder system are prepared by first preparing a mixture of binder resin and process water.
- formaldehyde-free refers to a reservoir composition that is substantially free of formaldehyde and/or does not liberate substantial amounts of formaldehyde as a result of curing or drying.
- the binder resin itself contains between 45 and 53% polymer solids with the balance being water.
- resin is then further diluted with water to yield a suitable binder composition.
- Acid is then added to the mixture to reduce the pH to about 3.5 or less.
- Other additives may be added to the mixture. The net result is a composition with significant amounts of water. While the water is helpful in ensuring proper application of the binder to the glass fiber, significant amounts of water can adversely affect curing.
- the invention is directed at a method of ensuring that the product that enters a curing oven has a moisture content less than the maximum amount the curing oven can tolerate and still produce an acceptable product.
- the method involves measuring the product moisture before it enters the curing oven and, depending upon the moisture value of the product, adjusting one or more process variables upstream of the curing oven.
- the formaldehyde-free binders are typically poly-carboxy polymers such as acrylic resins although any formaldehyde-free resin useful as a fiberglass binder may be used. They generally have a molecular weight of less than about 10,000, preferably less than about 5,000, most preferably less than about 3,000 with about 2,000 being advantageous.
- the polycarboxy polymer used in the binder of the present invention comprises an organic polymer or oligomer containing more than one pendant carboxy group.
- the polycarboxy polymer may be a homopolymer or copolymer prepared from unsaturated carboxylic acids including but not necessarily limited to, acrylic acid, methacrylic acid, crotonic acid, isocrotonic acid, maleic acid, cinnamic acid, 2- methylmaleic acid, itaconic acid, 2-methylitaeonic acid, .alpha. ,.beta.-methyleneglutaric acid, and the like.
- the polycarboxy polymer may be prepared from unsaturated anhydrides including, but not necessarily limited to, maleic anhydride, methacrylic anhydride, and the like, as well as mixtures thereof. Methods for polymerizing these acids and anhydrides are well-known in the chemical art.
- the formaldehyde-free curable aqueous binder composition of the present invention also contains a polyol containing at least two hydroxyl groups.
- the polyol must be sufficiently nonvolatile such that it will substantially remain available for reaction with the polyacid in the composition during heating and curing operations.
- the polyol may be a compound with a molecular weight less than about 1000 bearing at least two hydroxyl groups such as, for example, ethylene glycol, glycerol, pentaerythritol, trimethylol propane, sorbitol, sucrose, glucose, resorcinol, catechol, pyrogallol, glycollated ureas, 1 ,4-cyclohexane diol, diethanolamine, triethanolamine, and certain reactive polyols such as, for example, .beta.-hydroxyalkylamides such as, for example, bis[N,N-di( ⁇ - hydroxyethyl)]adipamide, as may be prepared according to the teachings of U.S. Pat.
- hydroxyl groups such as, for example, ethylene glycol, glycerol, pentaerythritol, trimethylol propane, sorbitol, sucrose, glucose, resorcinol, catechol, pyroga
- No. 4,076,917 hereby incorporated herein by reference, or it may be an addition polymer containing at least two hydroxyl groups such as, for example, polyvinyl alcohol, partially hydrolyzed polyvinyl acetate, and homopolymers or copolymers of hydroxyethylmethacrylate, hydroxypropylmethacrylate, and the like.
- the most preferred polyol for the purposes of the present invention is triethanolamine (TEA).
- the ratio of the number of equivalents of carboxy, anhydride, or salts thereof of the polyacid to the number of equivalents of hydroxyl in the polyol is from about 1/0.01 to about 1/3.
- An excess of equivalents of carboxy, anhydride, or salts thereof of the polyacid to the equivalents of hydroxyl in the polyol is preferred.
- the more preferred ratio of the number of equivalents of carboxy, anhydride, or salts thereof in the polyacid to the number of equivalents of hydroxyl in the polyol is from about 1/0.4 to about 1/1.
- the most preferred ratio of the number of equivalents of carboxy, anhydride, or salts thereof in the polyacid to the number of equivalents of hydroxyl in the polyol is from about 1/0.6 to about 1/0.8, and most preferably from 1/0.65 to 1/0.75.
- a low ratio, approaching 0.7:1 has been found to be of particular advantage in the present invention, when combined with a low molecular weight polycarboxy polymer and the low pH binder.
- the formaldehyde-free curable aqueous binder composition of the present invention also contains a catalyst.
- the catalyst is a phosphorous- containing accelerator which may be a compound with a molecular weight less than about 1000 such as, for example, an alkali metal polyphosphate, an alkali metal dihydrogen phosphate, a polyphosphoric acid, and an alkyl phosphinic acid or it may be an oligomer or polymer bearing phosphorous-containing groups such as, for example, addition polymers of acrylic and/or maleic acids formed in the presence of sodium hypophosphite, addition polymers prepared from ethylenically unsaturated monomers in the presence of phosphorous salt chain transfer agents or terminators, and addition polymers containing acid-functional monomer residues such as, for example, copolymerized phosphoethyl methacrylate, and like phosphonic acid esters, and copolymerized vinyl sulfonic acid monomers, and their salts.
- the phosphorous-containing accelerator may be used at a level of from about 1% to about 40%, by weight based on the combined weight of the polyacid and the polyol. Preferred is a level of phosphorous-containing accelerator of from about 2.5% to about 10%, by weight based on the combined weight of the polyacid and the polyol.
- fiberglass products are formed in a multi-step process.
- Molten glass is introduced from a furnace 11 through a spinner 12 that forms a plurality of fiberglass fibers 13 in a method well known in the art.
- the formaldehyde-free binder composition is sprayed onto the fibers by a plurality of spaced nozzles to form an uncured binder coated fiber.
- the coated fibers are then introduced into a collection box 14 that forms the fibers into an uncured pack or mat 15.
- the collection box 14 comprises a continuous moving belt or conveyor 16 that contains the uncured coated fibers 15 and moves them through the collection box to a second conveyor 17.
- the fibers are gathered onto the first conveyor 16 by pulling a large volume of air across a series of perforated plates on the conveyor 16 using one or more forming fans 18.
- the fibers form an uncured pack 15 on the first conveyor 16.
- a drop out box 19 slows down the velocity of air between the conveyor 16 and the fans 18 so that water and other materials which pass through the first conveyor 16 do not reach the fan 18.
- Much of the moisture in the product is removed in the collection box 14. A significant amount of moisture is removed by evaporation due to the heat from the molten fibers. Additional moisture is removed by the flow of air through the glass fibers during the forming process. The amount of heat in the collection box 14 as well as the rate of air flow in the box will affect the moisture present in the product as it leaves the collection box.
- moisture sensors 20 are placed immediately downstream of the collection box 14 and prior to the entrance of the curing oven 21.
- the measured moisture value is then transmitted to a control unit 22 when the measured moisture value to compared with a pre-set moisture value. If the measured value exceeds the pre-set value, the control unit 22 then causes a change in one or more upstream process conditions thereby causing a reduction in the residual moisture.
- the pre-set moisture values will depend on such factors as the nature of the binder system used, the desired properties of the finished product and the capacity of the curing ovens.
- the present moisture values for formaldehyde-free binder based products will be at least about 0 wt% to over 20 wt% with at least about 4 wt% to about 20 wt% preferred.
- the upper moisture value is limited primarily by the capacity of the oven to remove the moisture while still effectively curing the binder and the lower limit is generally determined based on product performance criteria and the nature of the binder.
- the control unit 22 relays a signal to the pump 22 that supplies process water to the system.
- control unit 22 causes the pump 23 to decrease the flow of process water thereby decreasing the water content of the binder composition. This, in turn, results in less residual moisture in the product before it enters the curing oven 20. Care should be taken, however, to ensure that a minimum level of water is added to properly prepare the binder composition.
- the moisture sensor 21 can be any moisture measurement system or device that can determine the percent of moisture present in the product. Preferred are indirect moisture sensors that do not interfere with the processing of the product and can provide continuous monitoring of moisture content.
- One particularly useful type sensor is the spectrographic sensor. These sensors measure moisture by exposing the sample to electromagnetic radiation at specific frequencies corresponding to characteristic absorptions of unbound water and measurement of either the absorbed or reflected reduction of the various spectroscopic techniques, microwave (MW) and Near Infrared (NIR) are preferred with NIR most preferred.
- the control unit 22 can be any system, method or device that can compare the measured moisture value with a pre-set value and then cause or reduce changes in one or more process variable.
- automatic, electronic systems such as Proportional Integral Derivative (PID) devices are preferred.
- PID Proportional Integral Derivative
- the moisture content is controlled by introducing additional heat into the collection box 14 to driving off the residual water.
- the control unit 22 sends a signal to the heating unit 24 which increases the temperature in the control unit thereby driving off any residual moisture.
- this temperature ranges from about 27 0 C to about 205 0 C with from about 65°C to about 150°C preferred that can be applied to the collection box in a number of methods the like.
- the additional heat can come from numerous sources including heating elements added to the collection box, hot air or water captured from other parts of the system and the like.
- Yet another method for controlling the pre-cured product moisture is by controlling the outflow through the product as it is formed in the collection box 14. Increased airflow reduces the residual moisture in the product.
- the forming fan 18 forces a stream of air through the fibers in the collection box 14 creating a mat of fibers 15. This air flow works to gather the fibers into the desired shape as they are formed and also forces residual water out of the product.
- the control unit 22 relays a signal to the forming fans 18 causing them to increase their speed thereby drawing more air through the fibers 15. This, in turn, pulls more moisture out of the product.
- both the heat and air flow can be increased together to reduce product moisture.
- the initial water added can be reduced and the air flow can be increased.
- Other combinations are readily apparent.
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Reinforced Plastic Materials (AREA)
- Surface Treatment Of Glass Fibres Or Filaments (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05770134A EP1784263A2 (en) | 2004-07-23 | 2005-07-07 | Control of pre-cured product moisture for formaldehyde-free fiberglass products |
CA002572339A CA2572339A1 (en) | 2004-07-23 | 2005-07-07 | Control of pre-cured product moisture for formaldehyde-free fiberglass products |
JP2007522531A JP2008507466A (en) | 2004-07-23 | 2005-07-07 | Control of product moisture before curing for formaldehyde-free glass fiber products |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/897,804 | 2004-07-23 | ||
US10/897,804 US7435444B2 (en) | 2004-07-23 | 2004-07-23 | Control of pre-cured product moisture for formaldehyde-free fiberglass products |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2006023137A2 true WO2006023137A2 (en) | 2006-03-02 |
WO2006023137A3 WO2006023137A3 (en) | 2006-08-24 |
Family
ID=35657510
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2005/024025 WO2006023137A2 (en) | 2004-07-23 | 2005-07-07 | Control of pre-cured product moisture for formaldehyde-free fiberglass products |
Country Status (6)
Country | Link |
---|---|
US (2) | US7435444B2 (en) |
EP (1) | EP1784263A2 (en) |
JP (1) | JP2008507466A (en) |
CN (1) | CN101014420A (en) |
CA (1) | CA2572339A1 (en) |
WO (1) | WO2006023137A2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2007128942A1 (en) * | 2006-05-10 | 2007-11-15 | Saint-Gobain Isover | Method for detecting localized defects present in a mineral fiber mat |
WO2019012232A1 (en) | 2017-07-13 | 2019-01-17 | Saint-Gobain Isover | Method for quantifying the moisture in a mat of fibres |
WO2020127784A1 (en) | 2018-12-21 | 2020-06-25 | Saint-Gobain Isover | Method for adjusting the amount of dilution water of a sizing composition, and corresponding calculcating unit |
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---|---|---|---|---|
US7258802B2 (en) * | 2004-07-09 | 2007-08-21 | Johns Manville | Method for controlling bacterial growth in process water |
US7718214B2 (en) * | 2006-11-01 | 2010-05-18 | Johns Manville | Method for producing fiberglass materials and compositions resulting from the same |
US20080175997A1 (en) * | 2007-01-19 | 2008-07-24 | Goldstein Joel E | Emulsion polymer binder with azirdine crosslinking agent for glass fiber webs |
US20100040832A1 (en) * | 2008-08-13 | 2010-02-18 | Saint-Gobain Technical Fabrics America, Inc. | Formaldehyde free woven and non-woven fabrics having improved hot wet tensile strength and binder formulations for same |
US20100197185A1 (en) * | 2009-01-30 | 2010-08-05 | Saint-Gobain Technical Fabrics America, Inc. | Low and ultra-low formaldehyde emission binders for non-woven glass mat |
FI20090319A0 (en) * | 2009-09-03 | 2009-09-03 | Beneq Oy | Process control method |
US8821625B2 (en) | 2010-12-09 | 2014-09-02 | Owens Corning Intellectual Capital, Llc | Apparatus and method for re-circulating wash water used in manufacturing glass fiber products |
US20120144868A1 (en) | 2010-12-09 | 2012-06-14 | Owens Corning Intellectual Capital, Llc | Apparatus and method for controlling moisture in the manufacture of glass fiber insulation |
US9128048B2 (en) | 2010-12-09 | 2015-09-08 | Owens Corning Intellectual Capital, Llc | Method for online determination of cure status of glass fiber products |
JP5876071B2 (en) * | 2010-12-09 | 2016-03-02 | オウェンス コーニング インテレクチュアル キャピタル リミテッド ライアビリティ カンパニー | Apparatus and method for controlling moisture during manufacture of glass fiber insulation |
US8718969B2 (en) | 2011-04-19 | 2014-05-06 | Owens Corning Intellectual Capital, Llc | Apparatus and method for continuous thermal monitoring of cure status of glass fiber products |
CN102809644A (en) * | 2011-06-01 | 2012-12-05 | 江西大华玻纤集团有限公司 | Method for simply detecting drying quality of glass fiber yarn |
US9133374B2 (en) | 2012-05-03 | 2015-09-15 | Georgia-Pacific Chemicals Llc | Resin systems for making composite products |
US20130292863A1 (en) * | 2012-05-03 | 2013-11-07 | Georgia-Pacific Chemicals Llc | Methods and systems for adjusting the composition of a binder system for use in making fiberglass products |
FR2994201B1 (en) | 2012-07-31 | 2014-08-08 | Saint Gobain Isover | PROCESS FOR COOKING A CONTINUOUS MATTRESS OF MINERAL OR VEGETABLE FIBERS |
JP2014208923A (en) * | 2013-03-27 | 2014-11-06 | セイコーエプソン株式会社 | Sheet manufacturing apparatus |
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US10684128B2 (en) | 2015-03-09 | 2020-06-16 | Alliance For Sustainable Energy, Llc | Batch and continuous methods for evaluating the physical and thermal properties of films |
US10889716B2 (en) | 2016-05-26 | 2021-01-12 | Georgia-Pacific Chemicals Llc | Binders containing an aldehyde-based resin and an isocyanate-based resin and methods for making composite lignocellulose products therefrom |
US11780112B2 (en) | 2016-05-26 | 2023-10-10 | Bakelite Chemicals Llc | Binders containing an aldehyde-based resin and an isocyanate-based resin and methods for making composite lignocellulose products therefrom |
US10988643B2 (en) | 2018-06-19 | 2021-04-27 | Johns Manville | Starch and carboxylic acid binder compositions and articles made therewith |
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2004
- 2004-07-23 US US10/897,804 patent/US7435444B2/en active Active
-
2005
- 2005-07-07 CN CNA2005800248294A patent/CN101014420A/en active Pending
- 2005-07-07 JP JP2007522531A patent/JP2008507466A/en not_active Withdrawn
- 2005-07-07 CA CA002572339A patent/CA2572339A1/en not_active Abandoned
- 2005-07-07 EP EP05770134A patent/EP1784263A2/en not_active Withdrawn
- 2005-07-07 WO PCT/US2005/024025 patent/WO2006023137A2/en active Application Filing
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2008
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WO2007128942A1 (en) * | 2006-05-10 | 2007-11-15 | Saint-Gobain Isover | Method for detecting localized defects present in a mineral fiber mat |
FR2901023A1 (en) * | 2006-05-10 | 2007-11-16 | Saint Gobain Isover Sa | METHOD OF DETECTING LOCALIZED DEFECTS IN A MATTRESS OF MINERAL FIBERS |
EA013200B1 (en) * | 2006-05-10 | 2010-04-30 | Сэн-Гобэн Изовер | Method for detecting localized defects present in a mineral fiber mat |
US8003946B2 (en) | 2006-05-10 | 2011-08-23 | Saint-Gobain Isover | Method for detecting localized defects present in a mineral fiber mat |
EP2018544B1 (en) | 2006-05-10 | 2016-08-10 | Saint-Gobain Isover | Method for detecting localized defects present in a mineral fiber mat |
NO340177B1 (en) * | 2006-05-10 | 2017-03-20 | Saint Gobain Isover | Method for detecting localized defects present in a mineral fiber mat. |
WO2019012232A1 (en) | 2017-07-13 | 2019-01-17 | Saint-Gobain Isover | Method for quantifying the moisture in a mat of fibres |
FR3069056A1 (en) * | 2017-07-13 | 2019-01-18 | Saint-Gobain Isover | METHOD OF QUANTIFYING MOISTURE IN A FIBER MATTRESS |
US11353408B2 (en) | 2017-07-13 | 2022-06-07 | Saint-Gobain Isover | Process for quantifying the moisture in a fiber blanket |
WO2020127784A1 (en) | 2018-12-21 | 2020-06-25 | Saint-Gobain Isover | Method for adjusting the amount of dilution water of a sizing composition, and corresponding calculcating unit |
FR3090623A1 (en) | 2018-12-21 | 2020-06-26 | Saint-Gobain Isover | Method for adjusting the amount of dilution water of a sizing composition, and corresponding calculation unit |
Also Published As
Publication number | Publication date |
---|---|
EP1784263A2 (en) | 2007-05-16 |
CA2572339A1 (en) | 2006-03-02 |
US20060019024A1 (en) | 2006-01-26 |
JP2008507466A (en) | 2008-03-13 |
US8003170B2 (en) | 2011-08-23 |
WO2006023137A3 (en) | 2006-08-24 |
US20090007644A1 (en) | 2009-01-08 |
CN101014420A (en) | 2007-08-08 |
US7435444B2 (en) | 2008-10-14 |
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