EP2010383A1 - Brandschutzverglasung - Google Patents
BrandschutzverglasungInfo
- Publication number
- EP2010383A1 EP2010383A1 EP07728236A EP07728236A EP2010383A1 EP 2010383 A1 EP2010383 A1 EP 2010383A1 EP 07728236 A EP07728236 A EP 07728236A EP 07728236 A EP07728236 A EP 07728236A EP 2010383 A1 EP2010383 A1 EP 2010383A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- layer
- intumescent
- glazing
- glazing according
- layers
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000011521 glass Substances 0.000 claims abstract description 18
- 239000004115 Sodium Silicate Substances 0.000 claims abstract description 10
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910052911 sodium silicate Inorganic materials 0.000 claims abstract description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 12
- 238000012360 testing method Methods 0.000 claims description 8
- 235000011187 glycerol Nutrition 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 229920005862 polyol Polymers 0.000 claims description 5
- 150000003077 polyols Chemical class 0.000 claims description 5
- 230000009970 fire resistant effect Effects 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims 2
- 229910052681 coesite Inorganic materials 0.000 claims 2
- 229910052906 cristobalite Inorganic materials 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- 235000012239 silicon dioxide Nutrition 0.000 claims 2
- 229910052682 stishovite Inorganic materials 0.000 claims 2
- 229910052905 tridymite Inorganic materials 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 20
- 239000011734 sodium Substances 0.000 description 20
- 239000000203 mixture Substances 0.000 description 19
- 239000000523 sample Substances 0.000 description 12
- 238000001035 drying Methods 0.000 description 10
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 150000004760 silicates Chemical class 0.000 description 5
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 4
- 238000010981 drying operation Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 235000019351 sodium silicates Nutrition 0.000 description 3
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- -1 amine compounds Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000010339 dilation Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004079 fireproofing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical class CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/02—Inorganic materials
-
- 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
Definitions
- the present invention relates to anti-fire glazing comprising glass sheets associated with one or more layers of hydrated alkali silicate.
- the exposure to fire of these glazings causes the formation of an opaque foam which opposes the transmission of radiation and maintains the glass sheets to which the alkali silicate layer (s) are associated.
- the invention relates more particularly to the glazings in question, the intumescent layer of which is prepared by drying an alkaline silicate solution.
- the invention is more particularly directed to glazings in which the intumescent layer consists of mainly sodium silicates.
- Fireproof glazing is qualified according to its resistance to standardized tests. Three qualities are analyzed, the flame-tightness (E), the radiation shield (W) and the insulation (I) formed by the foam developed by the silicate layer exposed to a high temperature rise. The classification is made according to the time during which the glazings tested offer the properties in question, as described in the standards EN1363, EN1364-1, EN13501-2 and EN357. Traditionally glazings are classified by 30 minutes of resistance: 30, 60, 90 minutes etc. These products carry the E, EW or EI mark according to whether they offer watertightness alone, watertightness and radiation shielding, or sealing and insulation. This symbol is followed by the number indicating the protection time in minutes.
- E 30 or EW 30 type the products for which the insulating nature is not particularly sought after, by far the vast majority of the products marketed are of the E 30 or EW 30 type.
- the E 60 or EW 60 products represent a much narrower market share, and superior resistance products do not are currently manufactured at the moment of demand and for very exceptional applications, and in the latter case most often in unusual small dimensions which make the required performance less difficult to achieve.
- glazings E (W) 30 and E (W) 60 are prepared under conditions that must be as economical as possible. For this reason the elements that constitute them must be standardized. For this reason in particular the layers of intumescent material are usually always prepared from the most common raw materials on the market and for this reason the least expensive.
- the basic raw material consists of solutions of alkali silicates which find applications in the most varied industries, cleaning products, paints ...
- solutions of alkaline silicates are characterized by a solids content of the order of 35% and a molar ratio SiO 2 / Na 2 O close to 3.3.
- the fluidity of these solutions and their stability over time contribute significantly to the choice of these solutions.
- intumescent layers from alkaline silicate solutions has developed logically from these most common products. This way of proceeding conditions the process of preparation of the layers and in particular the drying cycle to which the solution is subjected. In the experiment, the inventors have also found that this choice involves constraints and limitations with regard to the structures and qualities of the glazings comprising these intumescent layers. Nevertheless the benefit of the convenience of industrial implementation of a single product or at least a limited number of products (the silicate solutions indicated above) prevails. Reserving only a single or a small number of components, also producing only one type of layer or a limited number of intumescent layers in facilities operating in a given mode, have imposed themselves to practice.
- the inventors have shown that it is possible to meet the new requirements without modifying the structure of the previous glazings, conferring on the intumescent layers used a creep temperature "Td" increased. The measurement of this temperature is explained below.
- the intumescent layers based on sodium silicates used in the glazings according to the invention have a Td of not less than 440 ° C. and preferably not less than 450 ° C.
- the intumescent layers of the glazings the invention have a Td at least equal to 460 ° C.
- the Td increase of the intumescent layers according to the invention is advantageously obtained by the use of alkali silicates whose SiO 2 / Na 2 O molar ratio is at least 3.5, and preferably at least 3, 8.
- the increase of the SiO 2 / Na 2 O ratio is preferably obtained starting from solutions of commercially available silicates having the same ratio. If the most usual solutions have a ratio of the order of 3.3 as indicated above, it is possible to obtain solutions having a slightly higher ratio. The solicited producers thus propose solutions whose ratio is 3.85, and 4.1 and if necessary still a little higher. But starting from solutions of stable silicates prepared industrially, the ratio does not exceed 5. Beyond these values to remain stable, as indicated later, the solutions should be too diluted. Their use would then be discarded for reasons of cost of drying.
- the SiO 2 / Na 2 O molar ratio in the intumescent layers of the glazings according to the invention is in the range from 3.5 to 5 and preferably from 3.8 to 4.5.
- a typical glazing E 30 consists of two sheets of glass of 3mm each bound by an intumescent layer of 1.5mm.
- the characteristic "soft impact resistance" of this type of glazing can be sensitive to the modification of the ratio SiO 2 / Na 2 O.
- a typical glazing E 60 consisting for example of three sheets of glass respectively 3, 8 and 3mm thick, and two intumescent layers each 1.5mm thick, without difficulty retains the soft impact resistance required when you increase a little the SiO 2 / Na 2 O ratio.
- the compositions of the intumescent layers are characterized by a water content of 20 to 35% by weight of the layer, and preferably of 22 to 31%.
- the choice of these contents results from a compromise between the cost of the drying operations, the fireproofing properties and also the conditions which guarantee the transparency of the glazings at their production as well as over time.
- compositions used for the formation of the intumescent layers may contain sugars which complement the action of the polyols.
- Other traditional additives consist of TEOS (tetraethyl orthosilicate) or MTEOS (trimethoxy-methyl-silane) type compounds. These compounds are introduced into the layers in particular to improve the mechanical properties. Their introduction is at levels that do not exceed 3% by weight of the layer.
- the amine compounds preferably do not exceed 2% by weight of the layer.
- Other amino compounds such as TMAH (tetramethyl amine hydroxide) or a salt thereof, can improve aging behavior (haze).
- surfactants are frequently introduced into the initial compositions.
- the drying operation is carried out on a solution placed under a thin layer.
- the liquid composition is cast in the form of a film of uniform thickness on a support which can be conventionally constituted by a glass sheet intended to form part of the final glazing.
- the sheet covered by the solution is introduced into a chamber regulated temperature and humidity.
- the heated air circulating in the chamber gradually entrains part of the water contained in the solution.
- the drying can also be carried out in a known manner, the composition being deposited in a thin layer on a flexible support constituting a temporary support or not. In the first case the layer is separated after drying, in the second the flexible support can be incorporated in the final glazing with the intumescent layer that it supports during the drying operation.
- the drying of the solution is carried out until the water content is brought back to the values indicated above. It continues normally even after the solution has formed a gel.
- compositions and glazings comprising the intumescent layers prepared from these compositions.
- the temperature values "Td” are determined as follows.
- a glazing is formed of two sheets of glass between which is included the fireproof layer to be characterized.
- a 50mm square sample is cut from the side and pierced with a central hole 15mm in diameter.
- the sample is pre-expanded at 230 ° C. for 30 minutes and then cooled to room temperature.
- the Td measurement is carried out in a furnace (brand TONININDUSTRIE, model 5705) with temperature control, charging device, measuring thermocouples and differential measuring device.
- alumina shims the sample is positioned against the lower probe, which thus characterizes the lower face of the sample.
- the second probe passes through the sample through the central hole and thus characterizes the upper face of the sample.
- a load of 2.5kg is applied to the sample.
- differential measurement of the two probes one follows the dilation / compression of the sample when the temperature increases by 5 ° C / minute.
- the temperature Td is that at which the sample begins to flow, which results
- Example 1 The base composition consists of a sodium silicate solution having an SiO 2 / Na 2 O ratio of 3.9 and an initial water content of 70% by weight.
- the composition is applied to a glass sheet 3 mm thick.
- the creep temperature Td of the layer obtained is measured at 462 ° C.
- a "traditional" layer prepared under the same conditions but with a SiO 2 / Na 2 O ratio of 3.35 has a Td of 428 ° C.
- the laminated glazing thus constituted is arranged in a frame consisting of a simple steel profile, not insulated (model "Presto" marketed under the name
- the glazing according to the invention thus reaches 62 minutes.
- a composition analogous to that of Example 1 is prepared from a sodium silicate solution with a SiO 2 / Na 2 O 4 O ratio and a water content of 82% by weight.
- the solutions are dried as before.
- the intumescent layer prepared with a thickness of 1.8 mm has the following composition:
- the creep temperature of the layer thus produced is measured at 517 ° C.
- Glazing made as before with a central sheet of glass 8mm thick, subjected to the fire test has a resistance of 66 minutes.
- a composition analogous to that of Example 1 is prepared from a sodium silicate solution with an SiO 2 / Na 2 O 4 .15 ratio and a water content of 75% by weight.
- the solutions are dried as before.
- the prepared intumescent layer 1.1 mm thick, has the following composition: - 30% water
- the creep temperature of the thus produced layer is measured at 494 ° C.
- a glazing consisting as before of two sheets with the intumescent layer associated with a central sheet, subjected to the fire test has a resistance of 64 minutes.
- Example 1 Three sheets prepared in Example 1 are assembled with a fourth glass sheet 3 mm thick in a structure thus comprising 4 sheets of glass and 3 intumescent layers.
- the glazing thus formed subjected to the standard test withstands 72 minutes fire.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Joining Of Glass To Other Materials (AREA)
- Fireproofing Substances (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07728236A EP2010383A1 (de) | 2006-04-19 | 2007-04-18 | Brandschutzverglasung |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06112749 | 2006-04-19 | ||
| PCT/EP2007/053774 WO2007118886A1 (fr) | 2006-04-19 | 2007-04-18 | Vitrage anti-feu |
| EP07728236A EP2010383A1 (de) | 2006-04-19 | 2007-04-18 | Brandschutzverglasung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2010383A1 true EP2010383A1 (de) | 2009-01-07 |
Family
ID=36997913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07728236A Withdrawn EP2010383A1 (de) | 2006-04-19 | 2007-04-18 | Brandschutzverglasung |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP2010383A1 (de) |
| WO (1) | WO2007118886A1 (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE1019901A3 (fr) * | 2011-04-06 | 2013-02-05 | Agc Glass Europe | Vitrage resistant au feu. |
| WO2019158865A1 (fr) | 2018-02-16 | 2019-08-22 | Saint-Gobain Glass France | Vitrage anti-feu |
| WO2019158866A1 (fr) | 2018-02-16 | 2019-08-22 | Saint-Gobain Glass France | Procede de depot d'un revetement intumescent organique sur feuille de verre |
| FR3119844A1 (fr) | 2021-02-16 | 2022-08-19 | Saint-Gobain Glass France | Vitrage anti-feu comprenant une feuille de verre revêtue d’un revêtement intumescent |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58120548A (ja) * | 1982-01-08 | 1983-07-18 | Asahi Glass Co Ltd | 防火性ガラス板 |
| LU86691A1 (fr) * | 1986-12-01 | 1988-07-14 | Glaverbel | Panneau coupe-feu transparent |
| GB9116057D0 (en) * | 1991-07-24 | 1991-09-11 | Glaverbel | Light-transmitting fire-resistant panels |
| JPH0680461A (ja) * | 1991-08-03 | 1994-03-22 | Yasuo Yokoi | 耐熱性断熱組成物と耐熱性断熱材 |
| GB9721812D0 (en) * | 1997-10-15 | 1997-12-17 | Glaverbel | Transparent heat-swellable material |
| GB9721813D0 (en) * | 1997-10-15 | 1997-12-17 | Glaverbel | Heat-swellable material |
| CZ20013088A3 (cs) * | 1999-02-25 | 2002-10-16 | Vetrotech Saint-Gobain (International) Ag | Ohnivzdorná zasklívací sestava |
| DE19916506C1 (de) * | 1999-04-13 | 2000-07-13 | Flachglas Ag | Brandschutzglas |
| EP1577276A1 (de) * | 2004-03-05 | 2005-09-21 | Glaverbel | Verglasungsscheibe |
-
2007
- 2007-04-18 WO PCT/EP2007/053774 patent/WO2007118886A1/fr not_active Ceased
- 2007-04-18 EP EP07728236A patent/EP2010383A1/de not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2007118886A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007118886A1 (fr) | 2007-10-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20081029 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: AL BA HR MK RS |
|
| 17Q | First examination report despatched |
Effective date: 20090302 |
|
| RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: AGC GLASS EUROPE |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN |
|
| 18W | Application withdrawn |
Effective date: 20111102 |