US20050255323A1 - Fire resistant glazing - Google Patents
Fire resistant glazing Download PDFInfo
- Publication number
- US20050255323A1 US20050255323A1 US10/523,540 US52354005A US2005255323A1 US 20050255323 A1 US20050255323 A1 US 20050255323A1 US 52354005 A US52354005 A US 52354005A US 2005255323 A1 US2005255323 A1 US 2005255323A1
- Authority
- US
- United States
- Prior art keywords
- solution
- aluminate
- acid
- solution according
- interlayer
- 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
Links
- 230000009970 fire resistant effect Effects 0.000 title abstract description 13
- 235000019353 potassium silicate Nutrition 0.000 claims abstract description 51
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000011229 interlayer Substances 0.000 claims abstract description 42
- 150000004645 aluminates Chemical class 0.000 claims abstract description 31
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 24
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims abstract description 15
- -1 aluminium ions Chemical class 0.000 claims abstract description 9
- 239000004411 aluminium Substances 0.000 claims abstract description 8
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000000243 solution Substances 0.000 claims description 89
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 30
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 29
- 239000011521 glass Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 239000004115 Sodium Silicate Substances 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 11
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 11
- 239000004111 Potassium silicate Substances 0.000 claims description 10
- 229910052681 coesite Inorganic materials 0.000 claims description 10
- 229910052906 cristobalite Inorganic materials 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 claims description 10
- 229910052913 potassium silicate Inorganic materials 0.000 claims description 10
- 229910052682 stishovite Inorganic materials 0.000 claims description 10
- 229910052905 tridymite Inorganic materials 0.000 claims description 10
- ANBBXQWFNXMHLD-UHFFFAOYSA-N aluminum;sodium;oxygen(2-) Chemical compound [O-2].[O-2].[Na+].[Al+3] ANBBXQWFNXMHLD-UHFFFAOYSA-N 0.000 claims description 8
- 229910001388 sodium aluminate Inorganic materials 0.000 claims description 8
- 238000001035 drying Methods 0.000 claims description 7
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 5
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 5
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 claims description 4
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 230000003472 neutralizing effect Effects 0.000 claims description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 2
- NAOLWIGVYRIGTP-UHFFFAOYSA-N 1,3,5-trihydroxyanthracene-9,10-dione Chemical compound C1=CC(O)=C2C(=O)C3=CC(O)=CC(O)=C3C(=O)C2=C1 NAOLWIGVYRIGTP-UHFFFAOYSA-N 0.000 claims description 2
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 2
- 239000000174 gluconic acid Substances 0.000 claims description 2
- 235000012208 gluconic acid Nutrition 0.000 claims description 2
- 239000004310 lactic acid Substances 0.000 claims description 2
- 235000014655 lactic acid Nutrition 0.000 claims description 2
- 239000001630 malic acid Substances 0.000 claims description 2
- 235000011090 malic acid Nutrition 0.000 claims description 2
- 229910001414 potassium ion Inorganic materials 0.000 claims description 2
- 229910001415 sodium ion Inorganic materials 0.000 claims description 2
- 239000011975 tartaric acid Substances 0.000 claims description 2
- 235000002906 tartaric acid Nutrition 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 abstract description 3
- 238000010348 incorporation Methods 0.000 abstract 2
- 239000010410 layer Substances 0.000 description 10
- 235000011187 glycerol Nutrition 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 230000004888 barrier function Effects 0.000 description 5
- 239000005340 laminated glass Substances 0.000 description 5
- 239000013078 crystal Substances 0.000 description 4
- 239000005329 float glass Substances 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 238000006386 neutralization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000012445 acidic reagent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004320 controlled atmosphere Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- YQNQTEBHHUSESQ-UHFFFAOYSA-N lithium aluminate Chemical compound [Li+].[O-][Al]=O YQNQTEBHHUSESQ-UHFFFAOYSA-N 0.000 description 1
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 description 1
- 229910052912 lithium silicate Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- KVOIJEARBNBHHP-UHFFFAOYSA-N potassium;oxido(oxo)alumane Chemical compound [K+].[O-][Al]=O KVOIJEARBNBHHP-UHFFFAOYSA-N 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
- C03C17/28—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material
- C03C17/30—Surface treatment of glass, not in the form of fibres or filaments, by coating with organic material with silicon-containing compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10165—Functional features of the laminated safety glass or glazing
- B32B17/10311—Intumescent layers for fire protection
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/069—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of intumescent material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10009—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
- B32B17/10036—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising two outer glass sheets
-
- 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
- C03C17/00—Surface treatment of glass, not in the form of fibres or filaments, by coating
Definitions
- This invention relates to novel solutions useful in the production of fire resistant glazings comprising an alkali metal aluminate and a silicate waterglass, to methods for the preparation of those solutions and to the production of intumescent interlayers from those solutions which may be incorporated into fire resistant glazings.
- Glass laminates incorporating an intumescent inorganic silicate layer sandwiched between two opposed panes of glass are sold under the trade marks PYROSTOP and PYRODUR by the Pilkington group of companies. When such laminates are exposed to a fire the inorganic layer intumesces and expands to form a foam.
- the foam provides a thermally insulating layer which protects the pane of glass remote from the fire so that the structural integrity of the glass unit and thereby a barrier to the propagation of the fire is maintained for a longer period.
- Glass laminates incorporating such intumescent layers have been used successfully as fire resistant glass structures. These laminates may comprise more than two panes of glass sandwiching more than one intumescent interlayer.
- Laminates comprising up to eight intumescent layers have been employed. These multi layered laminates are relatively thick and correspondingly expensive.
- the intumescent inorganic layer is normally formed from a sodium silicate waterglass or a mixture thereof with a potassium silicate waterglass. The layer is commonly formed by preparing a solution of the waterglass (or waterglasses), spreading that solution on the surface of the glass and drying excess water from the solution so as to form the intumescent inorganic layer.
- U.S. Pat. No. 4,190,698 discloses fire resistant glazings comprising an intumescent inorganic layer obtained by drying a waterglass solution.
- the authors suggest the addition of various additives to the waterglass solution including urea, polyhydric alcohols, monosaccharides, polysaccharides, sodium phosphate, sodium aluminate, borax, boric acid and colloidal silica.
- urea polyhydric alcohols
- monosaccharides polysaccharides
- polysaccharides sodium phosphate
- sodium aluminate borax
- boric acid boric acid
- colloidal silica There is no specific disclosure of the addition of an aluminate to a waterglass solution.
- this invention provides a clear stable solution useful in the production of fire resistant glazings comprising an alkali metal silicate waterglass, a water soluble aluminate and a hydroxy caboxylic acid.
- the water soluble aluminate is preferably an alkali metal aluminate such as lithium aluminate, potassium aluminate, caesium aluminate and most preferably sodium aluminate.
- alkali metal aluminate such as lithium aluminate, potassium aluminate, caesium aluminate and most preferably sodium aluminate.
- Other water soluble aluminates notably ammonium aluminate and alkyl ammonium aluminates may also be employed.
- the carboxylic acid is preferably a hydroxy carboxylic acid and more preferably an ⁇ -hydroxy carboxylic acid.
- preferred carboxylic acids include tartaric acid, malic acid, gluconic acid, lactic acid, saccharic acid and most preferably citric acid.
- the waterglasses useful in the compositions of this invention are preferably sodium silicate waterglasses.
- the preferred sodium silicate waterglasses are those wherein the weight ratio of SiO 2 :Na 2 O is at least 2.0:1 more preferably at least 2.5:1 and most preferably at least 2.85:1.
- Sodium silicate waterglass solutions wherein the weight ratio of SiO 2 : Na 2 O varies between 2.0:1 and 4.0:1 are available as articles of commerce. Specifically solutions wherein this ratio is 2.0:1, 2.5:1 and 2.85:1 3.0:1 and 3.3:1 are available as articles of commerce.
- Waterglasses having any particular weight ratio of SiO 2 :Na 2 O may be produced by blending these commercially available waterglass solutions.
- Sodium silicate waterglasses having a weight ratio of SiO 2 :Na 2 O of 2.0:1, 2.5:1 and 2.85:1 are preferred for use in the present invention.
- Potassium silicate and lithium silicate waterglasses may also be used in the compositions of this invention.
- these waterglasses will be used as a partial replacement for the sodium silicate waterglasses.
- the molar ratio of sodium to potassium and/or lithium in the waterglass solution will be at least 2:1.
- the waterglass solution used in the present invention comprise a mixture of sodium silicate waterglass and a potassium silicate waterglass.
- the molar ratio of sodium ions to potassium ions in these mixtures in preferably at least 4:1.
- a potassium silicate waterglass is employed it is preferably one where the weight ratio SiO 2 : K 2 O is in the range 1.43:1 to 2.05:1.
- the solutions of this invention may further comprise one or more polyhydric compounds which are known to be useful in existing intumescent interlayers.
- Polyhydric compounds which have been proposed for this use include glycerol, glycerine or a derivative of glycerine or a sugar.
- the most commonly used polyhydric compound and the preferred polyhydric compound for present use is glycerol.
- the solution of this invention should preferably be clear, stable and capable of being dried to form a useful intumescent interlayer.
- the properties of the solution are affected by the composition of the solution and the methods used in their preparation. The utility of any particular solution may be determined by experiment.
- the stability of the solutions decreases as the amount of aluminate present increases.
- the fire resistance of the interlayer increases in proportion to the amount of aluminate present.
- the amount of aluminate which is incorporated into the solution will preferably represent a compromise between these two properties and will typically be such that the molar ratio of silicon to aluminium is in the range 20:1 to 35:1 more preferably in the rage 25:1 to 32:1.
- a second significant factor which affects the utility of the solutions of this invention is the weight ratio of silica to alkali metal oxide. Increasing the proportion of silica reduces the stability of the solution and is undesirable. The lower ratios of silicon to alkali metal are preferred since this increases the flow point of the dried interlayer which is an important factor influencing the performance of a glazing incorporating such an interlayer in fire testing. Generally we prefer that the weight ratio of silica to alkali metal oxide is in the range 2:1 to 4:1.
- the solutions of the present invention must be clear. They are prepared by mixing the various components in a manner which produces a clear stable solution which may then be dried to form a clear stable intumescent layer.
- the solutions are prepared using a process which comprises as a first step partially neutralising the aluminate with the hydroxy carboxylic acid.
- This neutralisation may be carried out by adding a hydroxycarboxylic acid solution to an aqueous solution of the aluminate.
- a hydroxycarboxylic acid solution may be added to an aqueous solution of the aluminate.
- the aluminate solution will preferably contain as high a solids content as is compatible with the production of a clear stable solution.
- the aluminate solution may typically comprise from 20 to 45% by weight of solids.
- the hydroxy carboxylic acid solution may be added to the aluminate either as a solid or as a solution.
- the solution may be an aqueous solution.
- the solutions of this invention comprise a polyhydroxy compound which is preferably glycerol the hydroxy carboxylic acid may be dissolved in the polyhydroxy compound and the resulting solution is used to neutralise the aluminate.
- the addition of the acid solution to the aluminate solution is preferably continued until the solution has a pH in the range 9.0 to 11.0 and more preferably in the range 9.5 to 10.0.
- the neutralisation should be carried out with thorough mixing and in a manner such that the temperature of the reaction mixture is not allowed to rise excessively and is preferably maintained below 50° C.
- Solutions which comprise a water soluble aluminate, a hydroxy carboxylic acid and a polyhydric compound which is preferably glycerol are believed to be novel and comprise a further aspect of the invention.
- the partially neutralised aluminate solution may be added to a solution comprising an alkali metal silicate waterglass to form a solution according to the present invention.
- the mixing of the aluminate with the waterglass must be carried out in a controlled manner so as to avoid the formation of any precipitate. We prefer to add the aluminate to the waterglass at a controlled rate with thorough mixing.
- the resulting solutions may be used in the production of five resistant glazings using known techniques.
- the solutions may be spread upon the surface of a glass sheet which is provided with an edge barrier which retains the solution on the surface of the glass.
- the quantity of solution employed will vary with the desired thickness of the dried interlayer. The quantity needed to produce an interlayer of any particular thickness may be determined by routine experiment.
- the solution is then dried under carefully controlled conditions of temperature and humidity so as to ensure the production of a clear transparent interlayer which is free from bubbles and other optical imperfections.
- the dried interlayers generally comprise form 10 to 35% by weight of water.
- the aluminium content of the dried interlayer is generally in the range 0.1% to 5.0% by weight preferably from 0.1% to 1.0% by weight. We have discovered that the presence of the aluminium improves the performance of glazings into which the interlayer is incorporated in terms of their fire resistance and their mechanical impact resistance properties.
- the thickness of the dried interlayer will generally be in the range 0.1 to 2.0 mm preferably from 0.5 to 2.0 mm.
- the formations of thicker interlayers requires a longer drying time and is thereby disadvantageous. Thinner interlayers can be produced using shorter drying times.
- a glass laminate having a thicker interlayer may be produced by bringing two sheets of glass each having a relatively thin interlayer having say a thickness of from 0.5 mm to 1.0 mm into face to face contact so as to form a laminate having an intumescent interlayer which is from 0.2 to 2.0 mm thick.
- Flat glass sheets of various thickness may be used in the laminates of the present invention.
- sheets of soda lime float glass having a thickness of from 2.0 mm to 4.0 mm are employed.
- a laminate may be formed by placing a second glass sheet on top of the interlayer.
- the second glass sheet may itself be one having an intumescent interlayer on one surface thereof. Mounting this second sheet on top of the first sheet so that the two fire resistant interlayers are in contact with each other produces a laminate having a relatively thick interlayer. Mounting the second sheet so that the interlayer is on its upper surface and subsequently providing a third glass sheet on top of that second interlayer produces a laminate having two interlayers mounted between three panes of glass. Laminates having as many as eight interlayers may be produced.
- the solutions of this invention may be poured onto the surface of the substrate and dried to form an intumescent fire resistant interlayer which is sufficiently strong to be removed from the substrate in the form of a transparent film.
- the film may then be placed between two sheets of glass to form a fire resistant glass laminate.
- substrates may be employed in processes of this type examples being glass sheets, metal sheets and polymeric materials such as PTFE and polyolefins such as polypropylene.
- a solution comprising a sodium aluminate, a sodium silicate waterglass, a potassium silicate waterglass and citric acid was made up using the following components:—
- a waterglass solution comprising a sodium silicate, a potassium silicate and glycerol was made up by mixing 151.7 parts by weight of Crystal 96 with 44.3 parts by weight of Crystal K120 and 20.5 parts by weight of glycerol.
- the mixed solution comprising the aluminate was then added to the waterglass solution.
- the addition was carried out by slowly adding the aluminate solution with thorough mixing using a Silverson high shear mixer.
- the resulting solution was clear and was stable on storage at room temperature.
- This solution was then applied to the surface of a sheet of float glass having an edge barrier around its perimeter in a quantity of 4 kilograms of solution per square metre of glass.
- the glass sheet was placed in an oven and dried over a prolonged period in a controlled atmosphere until the water content of the solution had reduced to 26% by weight.
- a clear interlayer having a depth of approximately 1.3 mm had formed on the surface of the glass.
- edge barrier was cut away and a second sheet of float glass having a thickness of 3 mm was placed on top of the interlayer to produce a glass laminate.
- Pieces of this laminate were tested for Fire Resistance according to B.S. 476 Part 20/2 and mechanical impact performance according to B.S 6206 Class C. Two pieces were subject to the fire test and both passed with times of 33 minutes and 30 minutes. Four pieces were tested for impact performance and all were rated at least a safe pass.
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- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Joining Of Glass To Other Materials (AREA)
- Laminated Bodies (AREA)
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Abstract
Fire resistant glazings comprise a fire resistant interlayer based upon a silicate waterglass are characterised by the incorporation of aluminium ions. The aluminate is incorporated as a solution which has been partially neutralised using hydroxycarboxylic acid which is preferably citric acid. The incorporation of aluminium provides glazings have improved fire resistance and impact properties.
Description
- This invention relates to novel solutions useful in the production of fire resistant glazings comprising an alkali metal aluminate and a silicate waterglass, to methods for the preparation of those solutions and to the production of intumescent interlayers from those solutions which may be incorporated into fire resistant glazings.
- Glass laminates incorporating an intumescent inorganic silicate layer sandwiched between two opposed panes of glass are sold under the trade marks PYROSTOP and PYRODUR by the Pilkington group of companies. When such laminates are exposed to a fire the inorganic layer intumesces and expands to form a foam. The foam provides a thermally insulating layer which protects the pane of glass remote from the fire so that the structural integrity of the glass unit and thereby a barrier to the propagation of the fire is maintained for a longer period. Glass laminates incorporating such intumescent layers have been used successfully as fire resistant glass structures. These laminates may comprise more than two panes of glass sandwiching more than one intumescent interlayer. Laminates comprising up to eight intumescent layers have been employed. These multi layered laminates are relatively thick and correspondingly expensive. The intumescent inorganic layer is normally formed from a sodium silicate waterglass or a mixture thereof with a potassium silicate waterglass. The layer is commonly formed by preparing a solution of the waterglass (or waterglasses), spreading that solution on the surface of the glass and drying excess water from the solution so as to form the intumescent inorganic layer.
- U.S. Pat. No. 4,190,698 discloses fire resistant glazings comprising an intumescent inorganic layer obtained by drying a waterglass solution. The authors suggest the addition of various additives to the waterglass solution including urea, polyhydric alcohols, monosaccharides, polysaccharides, sodium phosphate, sodium aluminate, borax, boric acid and colloidal silica. There is no specific disclosure of the addition of an aluminate to a waterglass solution.
- We have discovered that the addition of sodium aluminate to a waterglass solution as proposed in U.S. Pat. No. 4,190,698 does not produce a solution which is useful in the production of fire resistant glazings. The solutions are unstable and form a precipitate immediately or on standing. Since the dried interlayer must be optically clear the presence of particulate material such as this precipitate is not acceptable.
- Applicants have discovered that it is possible to produce a clear stable solution comprising an aluminate and a waterglass which can be used in the production of fire resistant glazings by partially neutralising the aluminate with a hydroxy carboxylic acid prior to mixing it with the waterglass. Thus from one aspect this invention provides a clear stable solution useful in the production of fire resistant glazings comprising an alkali metal silicate waterglass, a water soluble aluminate and a hydroxy caboxylic acid.
- The water soluble aluminate is preferably an alkali metal aluminate such as lithium aluminate, potassium aluminate, caesium aluminate and most preferably sodium aluminate. Other water soluble aluminates notably ammonium aluminate and alkyl ammonium aluminates may also be employed.
- The carboxylic acid is preferably a hydroxy carboxylic acid and more preferably an α-hydroxy carboxylic acid. Examples of preferred carboxylic acids include tartaric acid, malic acid, gluconic acid, lactic acid, saccharic acid and most preferably citric acid.
- The waterglasses useful in the compositions of this invention are preferably sodium silicate waterglasses. The preferred sodium silicate waterglasses are those wherein the weight ratio of SiO2:Na2O is at least 2.0:1 more preferably at least 2.5:1 and most preferably at least 2.85:1. Sodium silicate waterglass solutions wherein the weight ratio of SiO2: Na2O varies between 2.0:1 and 4.0:1 are available as articles of commerce. Specifically solutions wherein this ratio is 2.0:1, 2.5:1 and 2.85:1 3.0:1 and 3.3:1 are available as articles of commerce. Waterglasses having any particular weight ratio of SiO2:Na2O may be produced by blending these commercially available waterglass solutions. Sodium silicate waterglasses having a weight ratio of SiO2:Na2O of 2.0:1, 2.5:1 and 2.85:1 are preferred for use in the present invention.
- Potassium silicate and lithium silicate waterglasses may also be used in the compositions of this invention. In a preferred embodiment these waterglasses will be used as a partial replacement for the sodium silicate waterglasses. In general the molar ratio of sodium to potassium and/or lithium in the waterglass solution will be at least 2:1.
- In particular preferred embodiment the waterglass solution used in the present invention comprise a mixture of sodium silicate waterglass and a potassium silicate waterglass. The molar ratio of sodium ions to potassium ions in these mixtures in preferably at least 4:1. Where a potassium silicate waterglass is employed it is preferably one where the weight ratio SiO2: K2O is in the range 1.43:1 to 2.05:1.
- The solutions of this invention may further comprise one or more polyhydric compounds which are known to be useful in existing intumescent interlayers. Polyhydric compounds which have been proposed for this use include glycerol, glycerine or a derivative of glycerine or a sugar. The most commonly used polyhydric compound and the preferred polyhydric compound for present use is glycerol.
- In order to be useful in the production of intumescent interlayers the solution of this invention should preferably be clear, stable and capable of being dried to form a useful intumescent interlayer. The properties of the solution are affected by the composition of the solution and the methods used in their preparation. The utility of any particular solution may be determined by experiment. The stability of the solutions decreases as the amount of aluminate present increases. However the fire resistance of the interlayer increases in proportion to the amount of aluminate present. The amount of aluminate which is incorporated into the solution will preferably represent a compromise between these two properties and will typically be such that the molar ratio of silicon to aluminium is in the range 20:1 to 35:1 more preferably in the rage 25:1 to 32:1.
- A second significant factor which affects the utility of the solutions of this invention is the weight ratio of silica to alkali metal oxide. Increasing the proportion of silica reduces the stability of the solution and is undesirable. The lower ratios of silicon to alkali metal are preferred since this increases the flow point of the dried interlayer which is an important factor influencing the performance of a glazing incorporating such an interlayer in fire testing. Generally we prefer that the weight ratio of silica to alkali metal oxide is in the range 2:1 to 4:1.
- The solutions of the present invention must be clear. They are prepared by mixing the various components in a manner which produces a clear stable solution which may then be dried to form a clear stable intumescent layer.
- We prefer that the solutions are prepared using a process which comprises as a first step partially neutralising the aluminate with the hydroxy carboxylic acid. This neutralisation may be carried out by adding a hydroxycarboxylic acid solution to an aqueous solution of the aluminate. As the presence of excessive quantities of water may destabilise the silicate solutions of the invention and because in any event excess water is an additional load on the drying process used to form the intumescent interlayer the aluminate solution will preferably contain as high a solids content as is compatible with the production of a clear stable solution. The aluminate solution may typically comprise from 20 to 45% by weight of solids.
- The hydroxy carboxylic acid solution may be added to the aluminate either as a solid or as a solution. The solution may be an aqueous solution. In the preferred embodiments where the solutions of this invention comprise a polyhydroxy compound which is preferably glycerol the hydroxy carboxylic acid may be dissolved in the polyhydroxy compound and the resulting solution is used to neutralise the aluminate.
- The addition of the acid solution to the aluminate solution is preferably continued until the solution has a pH in the range 9.0 to 11.0 and more preferably in the range 9.5 to 10.0. The neutralisation should be carried out with thorough mixing and in a manner such that the temperature of the reaction mixture is not allowed to rise excessively and is preferably maintained below 50° C.
- Solutions which comprise a water soluble aluminate, a hydroxy carboxylic acid and a polyhydric compound which is preferably glycerol are believed to be novel and comprise a further aspect of the invention.
- The partially neutralised aluminate solution may be added to a solution comprising an alkali metal silicate waterglass to form a solution according to the present invention. The mixing of the aluminate with the waterglass must be carried out in a controlled manner so as to avoid the formation of any precipitate. We prefer to add the aluminate to the waterglass at a controlled rate with thorough mixing.
- The resulting solutions may be used in the production of five resistant glazings using known techniques. In one existing process the solutions may be spread upon the surface of a glass sheet which is provided with an edge barrier which retains the solution on the surface of the glass. The quantity of solution employed will vary with the desired thickness of the dried interlayer. The quantity needed to produce an interlayer of any particular thickness may be determined by routine experiment.
- The solution is then dried under carefully controlled conditions of temperature and humidity so as to ensure the production of a clear transparent interlayer which is free from bubbles and other optical imperfections. The dried interlayers generally comprise form 10 to 35% by weight of water. The aluminium content of the dried interlayer is generally in the range 0.1% to 5.0% by weight preferably from 0.1% to 1.0% by weight. We have discovered that the presence of the aluminium improves the performance of glazings into which the interlayer is incorporated in terms of their fire resistance and their mechanical impact resistance properties.
- The thickness of the dried interlayer will generally be in the range 0.1 to 2.0 mm preferably from 0.5 to 2.0 mm. The formations of thicker interlayers requires a longer drying time and is thereby disadvantageous. Thinner interlayers can be produced using shorter drying times. A glass laminate having a thicker interlayer may be produced by bringing two sheets of glass each having a relatively thin interlayer having say a thickness of from 0.5 mm to 1.0 mm into face to face contact so as to form a laminate having an intumescent interlayer which is from 0.2 to 2.0 mm thick.
- Flat glass sheets of various thickness may be used in the laminates of the present invention. Typically sheets of soda lime float glass having a thickness of from 2.0 mm to 4.0 mm are employed.
- The edge barrier is normally cut away at the completion of the drying process to leave a glass sheet having a dried interlayer on one surface. A laminate may be formed by placing a second glass sheet on top of the interlayer. In another embodiment the second glass sheet may itself be one having an intumescent interlayer on one surface thereof. Mounting this second sheet on top of the first sheet so that the two fire resistant interlayers are in contact with each other produces a laminate having a relatively thick interlayer. Mounting the second sheet so that the interlayer is on its upper surface and subsequently providing a third glass sheet on top of that second interlayer produces a laminate having two interlayers mounted between three panes of glass. Laminates having as many as eight interlayers may be produced.
- In an alternative process the solutions of this invention may be poured onto the surface of the substrate and dried to form an intumescent fire resistant interlayer which is sufficiently strong to be removed from the substrate in the form of a transparent film. The film may then be placed between two sheets of glass to form a fire resistant glass laminate. A variety of substrates may be employed in processes of this type examples being glass sheets, metal sheets and polymeric materials such as PTFE and polyolefins such as polypropylene.
- The invention is illustrated by the following example
- A solution comprising a sodium aluminate, a sodium silicate waterglass, a potassium silicate waterglass and citric acid was made up using the following components:—
- 1 A solution of a sodium silicate waterglass having a weight ration SiO2:Na2O of 2.85:1 and comprising 40% by weight of solids, sold by INEOS as Crystal 96.
- 2 A solution of a potassium silicate waterglass having a weight ration of SiO2:K2O of 1.43:1 comprising 52.4% by weight of solids; sold by INEOS as Crystal K120 potassium silicate
- 3 An aqueous solution of sodium aluminate comprising 38.0% by weight solids sold by Nordisk Aluminate
- 4 Glycerol—an 87% by weight solution in water
- 5 Citric acid—reagent grade
- The solutions were made up as follows:—
- First 5 parts by weight of citric acid were added to 10 parts by weight of glycerol with stirring so that the citric acid dissolved. The resulting solution is added slowly with vigorous stirring to 89.86 parts by weight of the sodium aluminate solution. The temperature of the solution was maintained below 50° C. throughout the addition. The resulting solution had a pH of 9.5.
- A waterglass solution comprising a sodium silicate, a potassium silicate and glycerol was made up by mixing 151.7 parts by weight of Crystal 96 with 44.3 parts by weight of Crystal K120 and 20.5 parts by weight of glycerol.
- The mixed solution comprising the aluminate was then added to the waterglass solution. The addition was carried out by slowly adding the aluminate solution with thorough mixing using a Silverson high shear mixer. The resulting solution was clear and was stable on storage at room temperature.
- This solution was then applied to the surface of a sheet of float glass having an edge barrier around its perimeter in a quantity of 4 kilograms of solution per square metre of glass. The glass sheet was placed in an oven and dried over a prolonged period in a controlled atmosphere until the water content of the solution had reduced to 26% by weight. A clear interlayer having a depth of approximately 1.3 mm had formed on the surface of the glass.
- The edge barrier was cut away and a second sheet of float glass having a thickness of 3 mm was placed on top of the interlayer to produce a glass laminate. Pieces of this laminate were tested for Fire Resistance according to B.S. 476 Part 20/2 and mechanical impact performance according to B.S 6206 Class C. Two pieces were subject to the fire test and both passed with times of 33 minutes and 30 minutes. Four pieces were tested for impact performance and all were rated at least a safe pass.
Claims (27)
1. A clear stable aqueous solution comprising an alkali metal silicate waterglass, a water soluble aluminate and a hydroxy carboxylic acid.
2. A solution according to claim 1 wherein the water soluble aluminate is an alkali metal aluminate.
3. A solution according to claim 1 wherein the water soluble aluminate is a sodium aluminate.
4. A solution according to claim 1 wherein the hydroxycarboxylic acid is an α-hydroxy carboxylic acid.
5. A solution according to claim 4 wherein the hydroxycarboxylic acid is selected from the group comprising tartaric acid, malic acid, gluconic acid, lactic acid, saccharic acid and citric acid.
6. A solution according to claim 5 wherein the hydroxycarboxylic acid is citric acid.
7. A solution according to claim 1 wherein the alkali metal silicate waterglass having a weight ratio SiO2:M2O of from 2.0:1 to 4.0:1 where M represents an alkali metal cation.
8. A solution according to claim 7 wherein the sodium silicate waterglass has a weight ratio SiO2:Na2O of from 2.5:1 to 3.0:1.
9. A solution according to claim 7 further comprising a potassium silicate waterglass
10. A solution according to claim 9 wherein the potassium silicate has a weight ratio SiO2:K2O of from 1.43:1 to 2.05:1.
11. A solution according to claim 9 wherein the molar ratio of sodium ions to potassium ions is at least 2:1.
12. A solution according to claim 1 wherein the molar ratio of silicon to aluminium is in the range 20:1 to 35:1.
13. A solution-according to claim 12 wherein the molar ratio of silicon to aluminium is in the range 25:1 to 32:1.
14. A solution according to claim 1 wherein the weight ratio of silica to alkali metal oxide is in the range 2:1 to 4:1.
15. A solution according to claim 1 further comprising a polyhydric compound.
16. A solution according to claim 15 wherein the polyhydric compound is glycerol.
17. A clear intumescent interlayer produced by drying a solution according to claim 1 under controlled conditions.
18. An interlayer according to claim 17 comprising from 10 to 35% by weight of water.
19. An interlayer according to claim 17 comprising from 0.1 to 5.0% by weight of aluminium.
20. An interlayer according to claim 17 wherein the interlayer has a thickness of form 0.5 to 2.0 mm.
21. A glass sheet having an interlayer according to claim 17 on one surface thereof.
22. A laminated glazing which comprises one or more interlayers according claim 17 and two or more sheets of glass.
23. A method for producing a solution according to claim 1 wherein a solution comprising a water soluble aluminate, a hydroxycarboxylic acid and a polyhydroxy compound is added to an alkali metal silicate solution.
24. A method according to claim 23 wherein the aluminate is sodium aluminate.
25. A method according to claim 23 wherein the hydroxycarboxylic acid is citric acid.
26. A method according to claim 23 wherein the polyhydroxy compound is glycerol.
27. A method according to claim 23 wherein the solution comprising the aluminate is formed by partially neutralizing the aluminate with the hydroxy carboxylic acid.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/552,097 US9789667B2 (en) | 2002-08-10 | 2009-09-01 | Fire resistant glazing |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0218672.4 | 2002-08-10 | ||
| GBGB0218672.4A GB0218672D0 (en) | 2002-08-10 | 2002-08-10 | Fire resistant glazings |
| PCT/GB2003/003434 WO2004014813A2 (en) | 2002-08-10 | 2003-08-06 | Clear stable aqueous solution based upon waterglass for the production of fire resistant glazing |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US12/552,097 Division US9789667B2 (en) | 2002-08-10 | 2009-09-01 | Fire resistant glazing |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20050255323A1 true US20050255323A1 (en) | 2005-11-17 |
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ID=9942120
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
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| US10/523,540 Abandoned US20050255323A1 (en) | 2002-08-10 | 2003-08-06 | Fire resistant glazing |
| US12/552,097 Expired - Lifetime US9789667B2 (en) | 2002-08-10 | 2009-09-01 | Fire resistant glazing |
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| Application Number | Title | Priority Date | Filing Date |
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| US12/552,097 Expired - Lifetime US9789667B2 (en) | 2002-08-10 | 2009-09-01 | Fire resistant glazing |
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| Country | Link |
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| US (2) | US20050255323A1 (en) |
| EP (1) | EP1558536B1 (en) |
| JP (1) | JP4445857B2 (en) |
| KR (1) | KR101076211B1 (en) |
| CN (1) | CN100455531C (en) |
| AU (1) | AU2003249079A1 (en) |
| CA (1) | CA2494194A1 (en) |
| GB (1) | GB0218672D0 (en) |
| RU (1) | RU2292375C2 (en) |
| WO (1) | WO2004014813A2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7334435B2 (en) * | 2000-09-20 | 2008-02-26 | Pilkington Plc | Production of fire resistant laminates |
| US20100129669A1 (en) * | 2006-10-31 | 2010-05-27 | Pilkington Group Limited | Fire resistant glazing |
| US20110183145A1 (en) * | 2006-10-31 | 2011-07-28 | Pilkington Group Limited | Method for the production of fire resistant glazings |
| US9080063B2 (en) | 2009-12-23 | 2015-07-14 | Pilkington Group Limited | Fire resistant glazings |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0614160A2 (en) * | 2005-07-26 | 2016-11-22 | Ineos Silicas Ltd | gel forming aqueous composition, application system for forming a coating composition and applying the coating composition thus formed on a substrate, substrate, aluminosilicate film, and methods of preparing a coating composition and coating, impregnating or otherwise applying on a substrate |
| PL1960317T3 (en) * | 2005-11-25 | 2018-07-31 | Agc Glass Europe | Fire-resistant glazing |
| DE102007002867B8 (en) * | 2007-01-15 | 2008-06-26 | Pilkington Deutschland Ag | Fire-resistant glazing |
| CH704939B1 (en) * | 2008-03-10 | 2012-11-15 | Akzo Nobel Chemicals Int Bv | Translucent heat protection element with aluminate or boratmodifiziertem silica. |
| EP2111977A1 (en) * | 2008-04-25 | 2009-10-28 | AGC Flat Glass Europe SA | Fireproof glazing |
| GB0915349D0 (en) | 2009-09-03 | 2009-10-07 | Pilkington Group Ltd | Fire resistant glazings |
| EP2305603B1 (en) * | 2009-10-05 | 2014-04-23 | Cognis IP Management GmbH | Soluble glass solutions containing aluminium |
| GB201115511D0 (en) | 2011-09-08 | 2011-10-26 | Pilkington Group Ltd | Fire resistant glazings |
| KR102207608B1 (en) * | 2019-04-24 | 2021-01-26 | 윤종오 | Process for producing silicon ion complexes and complexes organicized with carboxylic acid and products using the same |
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| US5519088A (en) * | 1991-07-18 | 1996-05-21 | Mitsui Toatsu Chemicals, Incorporated | Hardenable composition, aqueous gel and applications thereof |
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| GB226024A (en) * | 1923-12-01 | 1924-12-18 | William George Hay | Improvements relating to doll heads for drying cylinders |
| FR2549036B1 (en) * | 1983-07-11 | 1985-10-18 | Saint Gobain Vitrage | SAFETY SHEET GLAZING |
| GB2226024B (en) * | 1988-12-16 | 1992-06-10 | Tioxide Group Plc | Organo-metallic compounds |
| JP2987885B2 (en) | 1990-06-19 | 1999-12-06 | 三菱化学株式会社 | Method for producing flaky graphite fine particles |
| GB9918251D0 (en) * | 1999-08-04 | 1999-10-06 | Pilkington Plc | Fire resistant glazings |
| GB0006443D0 (en) * | 2000-03-18 | 2000-05-10 | Pilkington Plc | Fire resistant glazings |
| GB0023020D0 (en) * | 2000-09-20 | 2000-11-01 | Pilkington Plc | Production of fire resistant laminates |
-
2002
- 2002-08-10 GB GBGB0218672.4A patent/GB0218672D0/en not_active Ceased
-
2003
- 2003-08-06 CA CA002494194A patent/CA2494194A1/en not_active Abandoned
- 2003-08-06 KR KR1020057002161A patent/KR101076211B1/en not_active Expired - Lifetime
- 2003-08-06 JP JP2004527028A patent/JP4445857B2/en not_active Expired - Fee Related
- 2003-08-06 US US10/523,540 patent/US20050255323A1/en not_active Abandoned
- 2003-08-06 AU AU2003249079A patent/AU2003249079A1/en not_active Abandoned
- 2003-08-06 CN CNB03819063XA patent/CN100455531C/en not_active Expired - Lifetime
- 2003-08-06 EP EP03784262.2A patent/EP1558536B1/en not_active Expired - Lifetime
- 2003-08-06 RU RU2005106365/03A patent/RU2292375C2/en active
- 2003-08-06 WO PCT/GB2003/003434 patent/WO2004014813A2/en not_active Ceased
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- 2009-09-01 US US12/552,097 patent/US9789667B2/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4190698A (en) * | 1977-08-03 | 1980-02-26 | Bfg Glassgroup | Light-transmitting fire screening panel |
| US5216100A (en) * | 1989-12-18 | 1993-06-01 | Coatex S.A. | Non-toxic stabilizing agent for aqueous suspensions of sodium silico-aluminates |
| US5519088A (en) * | 1991-07-18 | 1996-05-21 | Mitsui Toatsu Chemicals, Incorporated | Hardenable composition, aqueous gel and applications thereof |
| US5624998A (en) * | 1991-07-18 | 1997-04-29 | Mitsui Toatsu Chemicals, Incorporated | Hardenable composition, aqueous gel and applications |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7334435B2 (en) * | 2000-09-20 | 2008-02-26 | Pilkington Plc | Production of fire resistant laminates |
| US20100129669A1 (en) * | 2006-10-31 | 2010-05-27 | Pilkington Group Limited | Fire resistant glazing |
| US20110183145A1 (en) * | 2006-10-31 | 2011-07-28 | Pilkington Group Limited | Method for the production of fire resistant glazings |
| US8932508B2 (en) | 2006-10-31 | 2015-01-13 | Pilkington Group Limited | Fire resistant glazing |
| US9080063B2 (en) | 2009-12-23 | 2015-07-14 | Pilkington Group Limited | Fire resistant glazings |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004014813A2 (en) | 2004-02-19 |
| RU2292375C2 (en) | 2007-01-27 |
| US20090317618A1 (en) | 2009-12-24 |
| CA2494194A1 (en) | 2004-02-19 |
| JP2005538015A (en) | 2005-12-15 |
| KR101076211B1 (en) | 2011-10-25 |
| CN1675138A (en) | 2005-09-28 |
| AU2003249079A1 (en) | 2004-02-25 |
| US9789667B2 (en) | 2017-10-17 |
| EP1558536A2 (en) | 2005-08-03 |
| JP4445857B2 (en) | 2010-04-07 |
| CN100455531C (en) | 2009-01-28 |
| GB0218672D0 (en) | 2002-09-18 |
| WO2004014813A3 (en) | 2004-03-25 |
| KR20050084801A (en) | 2005-08-29 |
| RU2005106365A (en) | 2005-09-10 |
| EP1558536B1 (en) | 2015-03-18 |
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| AS | Assignment |
Owner name: PILKINGTON PLC, UNITED KINGDOM Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:VARMA, KARIKATH SUKUMAR;HOLLAND, JOHN RICHARD;HOLDEN, DAVID WILLIAM;AND OTHERS;REEL/FRAME:016856/0146;SIGNING DATES FROM 20050124 TO 20050126 |
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