Patent Application
20170067248
The invention relates to panels and panel arrangements with fire barriers; methods of forming such panels and panel arrangements; fire barrier compositions; and reactants for forming fire barrier compositions.
Rigid polymer foams provide good thermal insulation and are thus used in building components such as “sandwich” pre-insulated panels. Such panels typically include a rigid polyurethane/polyisocyanurate (PU/PIR) foam core bonded to metal facing layers, for example of steel or aluminium, or stressed skins of metal foil. Panels of this type are available for example from SAB-Profiel™.
Such panels may be manufactured by a continuous process. A continuous lamination process typically uses a double belt/band arrangement wherein a liquid reaction mixture for forming a foamed polymer is deposited (poured or sprayed) onto a lower facing sheet, which may be flexible or rigid. An upper facing sheet is contacted with the polymer-forming mixture before it becomes cured and rigid. As an alternative (“inverse laminator”), the reaction mixture may be deposited onto the upper facing sheet. This process is discussed in “Polyurethane Handbook” (ed. Dr Guenter Oertel, Hanser Publishers 1985)1 US2005/02478993, US2007/0246160, WO2009/077490 and U.S. Pat. No. 4,019,938.
A thin layer of non-expanded or slightly expanded PU/PIR polymer formed from isocyanate and polyol is in some cases used to promote adhesion between the metal facing and the foam core. This thin layer is referred to as the “additional polyurethane/polyisocyanurate layer” (APL).
Lateral joints between panels are conventionally sealed with flexible foam gaskets.
Polymer foam core materials are typically combustible and leave little carbonaceous residue on burning. Thus, they provide only limited structural integrity under fire conditions. Structural integrity is important to prolong building stability and to maintain barriers to the passage of heat, smoke and fire.
The current fire resistance performance of metal faced sandwich panels, where the insulating layer is a PIR foam, is at best EI 60 on a 200 mm thick panel (where “EI” refers to integrity and insulation, and is followed by the number of minutes for which the component is effective). Reference standards are EN 1363-1/2 and EN 1364-1.
Attempts have been made to improve this performance, for example by incorporating flame retardant additives in the foam and by using incombustible thick facing materials (e.g. gypsum).
EP0891860 discloses a fire-resistant composite panel with a layer of intumescent mat (e.g. graphite based mineral fibre stabilized material) interposed between a core of rigid foamed plastics material and a metal outer layer. The mat is perforated with holes to permit bonding between the core and the metal layer.
The inventors have observed that when a typical sandwich panel is treated under furnace conditions, the steel facing quickly delaminates from the foam core and cracks appear in the foam.
In addition, it has been found that during a fire resistance test, damage typically occurs first at joints between panels, where insulation is lower. As a result, joints are weak areas which affect the fire resistance performance of the entire panel.
In a first aspect, the invention provides a panel comprising:
Preferably, the fire barrier layer comprises a dispersion in a polyurethane polymer matrix, polyurethane/polyisocyanurate polymer matrix or polyurethane/polyurea polymer matrix of at least one of porous silica; hollow glass microspheres; glass fibres and an inorganic ceramifying composition.
Preferably, the panel is self-supporting.
Fire Barrier Layer
The fire barrier layer(s) should provide good endurance of structural integrity and/or thermal barrier properties under fire conditions.
One, two, three or more fire barrier layer may be present. The structural integrity barrier and thermal barrier properties may be provided by separate layers (referred to as “structural integrity barrier layer” and “thermal barrier layer”) or by the same layer. Where these properties are provided by the same layer, they may be provided by different materials or by the same material.
Suitable fire barrier materials (i.e. materials for use in the fire barrier layer) are discussed below under the headings “Structural integrity barrier material”, “Thermal barrier material” and “Hybrid structural integrity barrier material and thermal barrier material” according to their properties.
Preferably, the fire barrier layer has a thermal conductivity (k) of less than 0.1 W/mK.
Preferably, the fire barrier is 2 to 20 mm (more preferably 2 to 15 mm, e.g. 3 to 10 mm) in thickness.
The fire barrier layer(s) is positioned between the foam core and the metal facing, and may conveniently be considered as a modified APL layer.
It is preferred for the fire barrier layer(s) to have good adhesive properties to the foam core and/or the metal facing. PU, PU/PIR and PU/polyurea polymers provide good adhesive properties, and are preferably used in the fire barrier layer(s) as discussed below. Where a fire barrier layer does not have good adhesive properties, a separate adhesive may be used.
Preferably, the fire barrier layer is continuous and is continuously bonded to the metal facing and to the insulating foam layer.
Structural Integrity Barrier Material
As explained above, one or more structural integrity barrier materials may be included in the fire barrier layer(s).
A structural integrity barrier material is intended to contribute to endurance of structural integrity in fire conditions. The suitability of a material to perform as structural integrity barrier material can be evaluated, for example, by placing a sample of the said material applied on a metal skin into a muffle heated with a temperature curve comparable to a fire resistance test and then verifying the absence of cracks and voids and checking for residual mechanical properties. The structural integrity barrier material preferably forms a coherent, strong char layer which will reduce the tendency of the underlying foam core to crack.
The structural integrity barrier material may include a particulate expandable under fire conditions.
Preferred structural integrity barrier materials for use in the fire barrier layer(s) are discussed below.
Ceramifying Mixture of Inorganic Compounds in Polymer Matrix
A dispersion of a ceramifying mixture of inorganic compounds in a polymer matrix can be used as a structure integrity barrier material in the fire barrier layer(s). Ceram Polymerik discloses such mixtures in WO2008134803, WO2005095545, WO2004088676 and WO2004035711.
The term “ceramifying composition” includes compositions which decompose and undergo chemical reaction under fire conditions to form a porous, self-supporting ceramic product. By contrast, conventional inorganic fillers remain as non-coherent particles under fire conditions.
Preferred mixtures include silicate minerals and inorganic phosphates. An additional inorganic filler and/or heat expandable material may be present. The ceramifying mixture may for example comprise some or all of aluminium trihydroxide, talc and ammonium polyphosphate. Examples of preferred mixtures include aluminium trihydroxide (ATH)/talc/ammonium polyphosphate (APP); talc/APP/zinc borate/expandable graphite. These materials react under fire conditions to form a coherent self-supporting ceramic once the activation temperature (typically within a range of 350 to 800° C.) reached.
Preferably, the polymer matrix is a PU/PIR polymer. Such polymers may be formed from a polyol (e.g. a polyester polyol) and an isocyanate (e.g. an organic polyisocyanate such as a polymeric methylene diphenyl diisocyanate, PMDI, e.g. 2.7 functionality). A catalyst is used. An appropriate index is 1.8 or more. The term “index” refers to the isocyanate index, a measure of the number of equivalents of isocyanate-containing compound added compared to the theoretical number of equivalents of isocyanate-containing compound needed. A higher index indicates a higher amount of isocyanate-containing reactant. Preferred polyols include Voramer® polyols (from The Dow Chemical Company).
Alternatively, the polymer matrix may be a polyurethane (PU) polymer, but this is less preferred. Such polymers may be formed from a polyol (e.g. a polyether polyol) and an isocyanate (e.g. an organic polyisocyanate such as a low functional PMDI, e.g. 2.7 functionality). A catalyst is used. An appropriate index is 0.8 to 1.8. Preferred polyols include Voranol® polyols (from The Dow Chemical Company).
Preferably, the ceramifying composition is present in an amount of 30 to 70 wt % based on the total weight of the layer.
Adhesive Polyurethane/Polyurea
An adhesive polyurethane/polyurea coating formed by reaction of sodium silicate aqueous solution (common name: water glass) with a hydrophilic prepolymer can be used as a structure integrity barrier material in the fire barrier layer(s). The coating has been found to form a cohesive char under exposure to fire. WO2006010697 (Huntsman) relates to such waterglass based PU/polyurea coatings. Other fire barrier materials may be dispersed in the coating.
A preferred hydrophilic polyurethane pre-polymer is a Dow Hypol® class isocyanate.
Glass Fibres
Glass fibres can be used as a structure integrity barrier material in the fire barrier layer(s). Chopped glass fibres of length 5 mm to 75 mm and/or diameter 10 to 13 μm are preferred. Alternatives to glass fibres include rock fibres, basalt fibres and carbon fibres. The fibres are preferably dispersed in a polymer matrix, for example a polymer matrix of the type discussed under “Ceramifying mixture of inorganic compounds in polymer matrix” above.
Thermal Barrier Material
As explained above, one or more thermal barrier materials may be included in the fire barrier layer(s).
A thermal barrier material provides a temperature gradient in fire conditions. This is intended to improve the insulation performance during the fire resistance test. The suitability of a material to perform as thermal barrier material can be evaluated in a laboratory scale using the testing procedure described below and shown in
Porous Silica
Porous silica can be used as a thermal barrier material in the fire barrier layer(s).
A preferred form of porous silica is nanoporous silica and particularly silica aerogel. Silica aerogel is a very low density nanoporous solid derived from silica gel by replacing liquid with gas, e.g by supercritical drying. It strongly absorbs infrared radiation and has outstanding thermal insulation characteristics. Synthesis of silica aerogel particles is discussed in WO2008115812 and WO9850144 of Cabot.
Porous silica is preferably used dispersed in a polymer matrix. The polymer matrix may be pre-formed or may be formed in situ.
Pre-formed dispersions of nanoporous silica in polymer matrix are commercially available as “aerogel blankets” e.g. Cabot Thermal Wrap™. These can comprise granules of silica aerogel dispersed in non-woven polymer fibres e.g. of polyethylene and/or polyester. Thermal Wrap™ is a flexible, compressible, low-lambda material that can be easily cut with scissors to tailored dimensions.
Dispersions of nanoporous silica in a polymer matrix may be formed in situ using commercial silica aerogel powder. A commercial silica aerogel nanoporous powder is Cabot Nanogel™.
Preferably, the porous silica is dispersed in a hydrophilic polymer matrix. Pure silica aerogel has outstanding thermal insulation characteristics (low lamda values) because of its nanoporous structure. Silica aerogel is expected to lose its outstanding thermal insulation characteristics when used in a polymer matrix, because the polymer will fill the nanoporous structure. However, the present inventors have appreciated that hydrophilic polymers and aqueous solutions will not fill the pores because of the hydrophobicity of the nanoporous silica. Thus, hydrophilic polymers and aqueous compositions used to provide such polymers can be used to avoid filling the pores of the nanoporous silica contained in the thermal barrier layer.
An adhesive polyurethane/polyurea coating with structural integrity barrier properties of the type discussed above is particularly suitable.
Alternatively, a PU/PIR or PU coating of the type discussed under “Ceramifying mixture of inorganic compounds in polymer matrix” above may be used.
WO2007047970 and WO9615998 relate to silica aerogel composites with an aqueous binding agent, and WO03097227, US2004077738, US2003215640 and EP1787716 relate to silica aerogel composites with hydrophilic binders. WO2007146945 (Aspen) relates to a PU/silica aerogel co-foam. WO2007086819 (Aspen) relates to a composite of poly(methyl methacrylate) (PMMA) and silica aerogel.
Preferably, the porous silica is present in an amount of 1 to 10 wt % based on the total weight of the layer.
Expandable Graphite
Expandable graphite (also referred to as “exfoliating graphite”) can be used as a thermal barrier material in the fire barrier layer(s).
Expandable graphite is a particulate expandable under fire conditions. Preferably, the expandable graphite particles are of mean particle size 200 to 300 μm. The expandable graphite is preferably dispersed in a polymer matrix, for example a polymer matrix of the type discussed under “Ceramifying mixture of inorganic compounds in polymer matrix” above.
Hybrid Structural Integrity Barrier Material and Thermal Barrier Material
As mentioned above, the structural integrity barrier and thermal barrier properties may be provided by a single material. Preferred such materials are discussed below.
Hollow Glass Microspheres
Hollow glass microspheres can be used as a hybrid structural integrity barrier material and thermal barrier material in the fire barrier layer(s). Suitable materials are discussed in WO2010065724, and are commercially available e.g. S35 Glass Bubbles™ from 3M. The inventors have found that the particles form a cohesive, cellular char of amorphous silica under flaming conditions. The particles are preferably used in a polymer matrix, e.g. using one of the polymer materials discussed above.
Preferably, the hollow glass microspheres have an average diameter in the range of 10 to 120 μm.
Preferably, the hollow glass microspheres are present in an amount of 5 to 50 wt % based on the total weight of the layer. In a preferred embodiment, a PU/PIR adhesive layer is filled with 20 wt % S35 microspheres.
Preferred Fire Barrier Structures
Preferred fire barrier structures (i.e. preferred fire barrier layers or combinations of fire barrier layers) include:
Facing
As explained above, the panel includes a first metal facing. Typically, a second metal facing is included in the panel on the opposite face from the first metal facing. Each metal facing is preferably of steel or aluminium. Preferably, each metal facing is 0.2 to 1.2 mm in thickness.
Foam Core
As explained above, the panel includes an insulating foam layer (also referred to as a foam core). Suitably, the foam core is rigid. Preferably, the foam core is 20 to 250 mm in thickness.
The foam core is preferably of PU/PIR. Preferred foams are formed from polyol (added with a blowing agent and a catalyst) and an isocyanate (e.g. an organic polyisocyanate such as high functional PMDI). A preferred index is 1.8 or more. Preferred polyols include Voratherm® polyols (from The Dow Chemical Company) which provide foams with good fire performance properties.
Manufacturing Process
In a second aspect, the invention provides a method of forming a panel as described above, comprising the steps of:
The fire barrier layer(s) may be provided in liquid form, and preferably at least one fire barrier layer is applied in the form of a liquid reaction mixture (optionally containing dispersed material) which will form a polymer matrix. Preferably, the liquid reaction mixture is an isocyanate-based reaction mixture, more preferably a dispersion in an isocyanate-based reaction mixture of at least one of porous silica; hollow glass microspheres; glass fibres; an inorganic ceramifying composition; expandable graphite.
Additionally or alternatively, at least one fire barrier layer (e.g. a dispersion of porous silica in a pre-formed polymer matrix) is applied in solid form. The fire barrier layer in solid form may be secured with an adhesive composition. However, if a previous fire barrier layer has been applied in liquid form an adhesive composition may not be necessary.
In a third aspect, the invention provides a method of forming a panel comprising: first and second metal facings; an insulating foam layer; and at least one fire barrier layer between the metal facing and the foam layer, the fire barrier layer(s) comprising at least one of porous silica; hollow glass microspheres; glass fibres, rock fibres, basalt fibres or carbon fibres; an inorganic ceramifying composition; a dispersion in a polyurethane polymer matrix or polyurethane/polyisocyanurate polymer matrix or polyurethane/polyurea polymer matrix of expandable graphite, the method comprising the steps of:
Panels in accordance with the invention may be manufactured in a continuous or discontinuous process.
Suitably, a PU/PIR adhesive is used and is applied in liquid form.
A discontinuous process using moulds may be used. In such a method, the metal facings are suitably positioned in a mould (preferably a heated mould) and the reaction mixture for forming the insulating form layer injected (e.g. using a foaming machine) so as to fill the mould and adhere to the metal facings. The fire barrier layer(s) may be added before the metal facings are positioned in the mould or while the metal facings are in the mould. Where there is more than one fire barrier layer, the layers may be formed in any order on the metal facing. However, it is preferably to have a thermal barrier material adjacent to the foam core.
Joint Fire Barrier
In a fourth aspect, the invention relates to a panel arrangement comprising:
wherein the fire barrier material comprises at least one of porous silica; hollow glass microspheres; glass fibres; an inorganic ceramifying composition; a dispersion in a polyurethane polymer matrix or polyurethane/polyisocyanurate polymer matrix or polyurethane/polyurea polymer matrix of expandable graphite.
Suitable joint fire barrier materials are the fire barrier materials discussed above.
In a fifth aspect, the invention relates to a method of forming a panel arrangement as described above, comprising the steps of:
Suitably, panels are mounted with overlapping portions e.g. a panel having a male portion along its edge may be mounted to a panel having a complementary female portion along its edge. The panels may be mounted to one another and/or to the building structure. The panels are preferably joined by friction fit and/or using screws.
Optionally, a gasket is also positioned in the joint region. The gasket may be formed of foam, and is preferably formed of flexible foam. The gasket is typically fed from rolls during panel production.
The fire barrier material is preferably applied in the form of a liquid reaction mixture to the joint region, for example by pouring or spraying. This may be done after panel production or on site before panel installation. Two or more fire barrier materials may be included, for example by including two or more fire barrier layers.
In a sixth aspect, the invention relates to a fire barrier composition comprising:
Preferred amounts of the various fire barrier materials in the fire barrier composition are as follows:
2-9 wt % porous silica;
20-60 wt % ceramifying composition;
5-15 wt % hollow silica microspheres.
In a seventh aspect, the invention relates to a reactant for forming a fire barrier composition comprising:
Preferred amounts of the various fire barrier materials in the reactant are as follows:
3-10 wt % porous silica;
40-80 wt % ceramifying composition;
10-20 wt % hollow silica microspheres.
Features described in connection with any aspect of the invention can be used in combination with any other aspect of the invention.
The invention will be further described with reference to the following non-limiting examples.
Materials
Polyurethane/Polyisocyanurate Foam Core
A bi-component system comprising (A) a polyol including a blowing agent and a catalyst and (B) a polymeric isocyanate PMDI is used for the foam core. Voratherm® CN 604 polyol (A) is reacted with a high functional PMDI (B) at index 2.85. Voratherm® CN 604 is a commercial product of The Dow Chemical Company.
Polyurethane/Polyisocyanurate Adhesive Layer
A bi-component system comprising (A) a polyol added with a catalyst and (B) a polymeric isocyanate PMDI is used for fire barrier layer(s). Voramer® MB 3171 polyol (A) is reacted with a 2.7 functionality PMDI (B) at index 2.00. Voramer® MB 3171 is a commercial product of The Dow Chemical Company.
Polyurethane Adhesive Layer
A bi-component system comprising (A) a polyol (B) a polymeric isocyanate PMDI is used for fire barrier layer(s). Voranol® CP 450 polyol (A) is reacted with a 2.7 functionality PMDI (B) at index 1.00. Voranol® CP 450 is a commercial product of The Dow Chemical Company.
Polyurethane/Polyurea Adhesive Layer
A polyurethane/polyurea adhesive coating is obtained by reacting (A) a sodium silicate solution in water (common name: water glass) and (B) an isocyanate-capped polyurethane (prepolymer). As the (A) part a 37 wt. % sodium silicate solution in water from Sigma-Aldrich Inc. is used; as the (B) part Hypol® JM 5002 prepolymer is used. Hypol® JM 5002 is a commercial product by The Dow Chemical Company.
Filler: Ceramifying Composition
A blend of inorganic minerals known to undergo sintering at high temperature (commercial name: Ceram Polymerik FM3H®) is purchased from Ceram Polymerik Ltd. The material, a white, fine powder, is used as received and without any further purification. It is believed to contain ATH/talc/APP.
Filler: Kaolin Powder
Kaolin (anhydrous aluminum silicate, Al2Si2O5(OH)4) powder (average particle size 3.8 μm) is purchased from READE® Advanced Materials. The material is used without any further purification.
Filler: Portland Cement
Portland Cement (commercial name: Laterlite® Leca CS 1600) is purchased from Laterlite S.p.A. (Milan) and used without any further purification.
Filler: Silica Aerogel Powder
A powdered silica aerogel (commercial name: Cabot Nanogel® TLD102) is purchased from Cabot Corporation and used without any further purification. The used grade shows relatively broad-size granules (up to 1.2 mm in diameter) having an average density of 80-90 kg/m3.
Filler: Glass Bubbles
Hollow glass microspheres are purchased from 3M company. The spheres are commercially available under the trade name of 3M Glass Bubbles S35™; their density is 350 kg/m3.
Filler: Expandable Graphite
Expandable graphite is obtained from Nordmann Rassmann. The product is commercially available under the trade name of Nord-Min® KP 251. It has a mean particle size of 250 μm.
Filler: Glass Fibres
Chopped glass fibres (25 mm long and 12 μm in diameter) are obtained from Hainan Fuwang Industrial Co. Ltd of China.
Blanket: Silica Aerogel Blanket
A commercial silica aerogel blanket (commercial name: Cabot Thermal Wrap®; thickness: 6 mm) is purchased from Cabot Corporation and used without any treatment. The blanket consists of Nanogel® granules within non-woven fibres of polyethylene and polyester.
Blanket: Mineral Wool Blanket
A commercial mineral wool blanket (commercial name: Rockwool® 234; thickness: 20 mm) is purchased from Rockwool Italia S.p.A. and used without any treatment.
Procedures
Mould Setup
The mould arrangement is shown in
In an aluminium mould 10 (30×30×10 cm) having walls thermostatically maintained at 50° C., a 20×20 cm steel plate 12 (thickness 0.4 mm; lower steel facing) is centered at ˜5 cm from the mould walls. Four 20×10×10 cm aluminium spacers 14 are placed on the top of the steel plate 12 and all along the mould borders; a central 10×10×10 cm hole 16 remains in the mould 10.
Four strips of commercially available adhesive tape 18 are attached parallel to the steel plate 12 at 45° to the edges of the aluminium mould 10 at the upper corners of the central hole 16. Another 10×10 cm steel plate 20 (thickness 0.4 mm; upper steel facing) is placed on the taped corners to close the mould 10.
After 1 hour the temperature of the spacers 14 is checked with a thermocouple; the mould 10 is then closed again until the temperature reaches 50° C. When this temperature is reached, the mould 10 is opened and the upper steel facing 20 is temporarily removed for foam pouring.
Production of Small-Scale Panels
The fire barrier layer(s) and the foam core are prepared in the mould. To form the first fire barrier layer B (structural integrity barrier layer or combined structural integrity barrier and thermal barrier layer), the polyol or water glass composition is obtained by hand mixing the components; after the addition of the isocyanate, 40 g of the reaction mixture is quickly poured into the central hole 16 in the mould 10 on top of the lower steel facing 12/A.
Where a second fire barrier layer C (thermal barrier layer) is to be formed from a liquid reaction mixture, it is prepared in the same way. 40 g of the reaction mixture is poured on top of the first fire barrier layer B in the central hole 16 in the mould 10 no more than 20 s after the pouring of the first fire barrier layer. Alternatively, where a blanket (silica aerogel blanket or mineral wool blanket) is used as the second fire barrier layer, it is gently placed on the top of the first fire barrier layer no more than 20 s after pouring.
The PU/PIR foam layer D is prepared by hand mixing the components, and pouring the reaction mixture on the top of the fire barrier layer(s). Where the upper fire barrier layer is poured, this should be done within 20 s of pouring.
After pouring of the foam composition, the upper steel facing 20/A is quickly positioned, and the mould 10 is closed before the PU/PIR foam reaches the upper steel facing 20/A.
After 10 minutes of reaction, the mould 10 is open and the small-scale panel 22 is removed from the mould (
Production of small-scale panel arrangements Small-scale panel arrangements with joint regions (Example 4,
The fire barrier material B is formed by hand mixing the components in a cup and pouring the liquid reaction mixture onto the female edge portion 44 of one panel strip. The second panel strip is then immediately placed in position to take advantage of the adhesive properties of the fire barrier material B.
Thus, a panel arrangement 46 of area 20×20 cm is produced (
Characterisation of Fire Resistance Properties of the Small-Scale Panels and Small-Scale Panel Arrangements
This process is summarised in
A small-scale panel 22 is supported on a steel frame 24 (
Damage is measured at the end of the trial as damaged height. The small-scale test is used to provide indicative results.
A similar small-scale fire test is used to test fire barrier materials in the joint regions between panels (Example 4).
Creation of Panels for Medium-Scale Fire Resistance Test
60×60×8 cm sized metal faced sandwich elements are produced. The fire barrier layer(s) are distributed on metal facings using a low pressure foaming machine combined with an air spray mixing head device. The metal facings are then placed in a mould. The PIR reaction mixture is injected into the heated mould using a high pressure foaming machine.
Characterization of Fire Resistance Properties in the Medium-Scale Test
The 60×60 cm sandwich panels are tested using a furnace capable of following the temperature/time curve of the EN 1363-1 standard. The temperature on the “cold” side of the sandwich is recorded vs. time in the central position of the surface. The results from the medium-scale test are more reliable than those from the small-scale test.
a multilayer sandwich panel as in
a sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
a multilayer sandwich panel as in
The composition of the panels tested is reported in Table 1 (Example 1) and Table 2 (Examples 2 and 3).
The internal temperatures of the samples after 15 and 30 minutes of flaming in the small-scale fire test, along with the height of the internal damage after cutting the foam, are reported in Table 3 (Example 1) and Table 4 (Examples 2 and 3).
The internal temperatures provide an indication of thermal barrier properties. The damage height provides an indication of structural integrity barrier properties. In the case of each of these variables, low values are desirable.
The small-scale fire test involves severe conditions because the testing thermocouple is only 5 cm from the flame source. Therefore, the fire barrier effect does not apply for as long as 30 minutes.
The temperature on the “cold” side of the sandwich exposed to the medium-scale fire resistance test after 15, 30 and 40 minutes is reported in Table 5 (Example 1-1, Comparative Example 1-2, Examples 2-1 and 2-2).
From Tables 3 and 4 it can be seen that where both structural integrity barrier and thermal barrier materials (hybrid or separate) are present (Examples 2-1, 2-5 and 3), very good results are achieved in the small-scale fire test. Temperatures after 15 minutes are in the range of 46 to 69° C. Damage height (where measured) is in the range of 55 to 61 mm. This is compared with a temperature after 15 minutes of 108° C. and a damage height of 63 mm for the control with an unmodified APL (Comparative Example 1-3).
From Table 3 it can also be seen that a fire barrier including a dispersion of ceramifying composition in PU/PIR as the structural integrity barrier material gave the lowest damage height (62 mm) and gave a lower temperature after 15 minutes (73° C.) than fire barriers using kaolin or Portland cement (Example 1-1 and Comparative Examples 1-4 and 1-5). A low temperature after 15 minutes (69° C.) was also achieved using a fire barrier including a dispersion of chopped glass fibres in PU/PIR as the structural integrity barrier material. Kaolin and Portland cement are used as fillers in WO2006010697.
From Table 4 it can also be seen that the use of a silica aerogel blanket gave a lower damage height (64 mm) and gave a lower temperature after 15 minutes (69° C.) compared with the use of a mineral wool blanket (Example 2-4 and Comparative Example 2-7).
From Table 5 it can be seen that hollow silica microspheres (Example 2-1), aerogel (Example 2-2) and a dispersion of expandable graphite in PU/PIR (Example 2-6) provided good performance in the medium-scale fire test. Results at 15 minutes in the medium-scale fire test are less significant than those at 30 and 40 minutes. The Example 2-1 fire barrier was found to delay the insulation failure by about 20 minutes, leading to 1=55 performance (EN test referred to above). Observations of the burnt panels showed a dense, coherent char on the exposed side, with cracks of reduced depth in the PIR foam beneath.
panels with joint region as in
panels with joint region as in
panels with joint region as in
The panels are submitted to the modified version of the small scale fire test described above.
The results of Example 4 are shown in Table 6.
From Table 6 it can be seen that where a fire barrier layer is included in the joint region (Examples 4-2 and 4-3), good results are achieved in the fire test compared with the results where a fire barrier is not included in the joint region (Comparative Example 4-1).
Proposed further examples:
panels with joint region as in
panels with joint region as in
panels with joint region as in
The panels of the preferred embodiments of the invention make use of a multilayer-multifunction concept to combine structural integrity barrier and thermal barrier properties. Very good fire resistance properties are achieved. The findings can also be applied to joint protection.
Moreover, the panels of the preferred embodiments of the invention are easy to manufacture. This is an improvement compared with WO2006010697, where the waterglass chemistry is difficult to use in a continuous production process because of lack of adhesion between the waterglass-based and metal layers. The use of PU/PIR in the fire barriers of preferred embodiments of the invention allows good adhesion to the metal facing and to the PIR foam core.
Whilst the invention has been described with reference to the illustrated preferred embodiments and the Examples, the skilled person will appreciate that various modifications are possible within the scope of the claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 11425251.3 | Oct 2011 | EP | regional |
| PCT/EP2012/068069 | Sep 2012 | EP | regional |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 14346877 | Mar 2014 | US |
| Child | 15265491 | US |
