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
  • C03C17/22—Surface treatment of glass, not in the form of fibres or filaments, by coating with other inorganic material
  • C03C17/23—Oxides
• • 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
• • 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
• • E—FIXED CONSTRUCTIONS
  • E06—DOORS, WINDOWS, SHUTTERS, OR ROLLER BLINDS IN GENERAL; LADDERS
  • E06B—FIXED OR MOVABLE CLOSURES FOR OPENINGS IN BUILDINGS, VEHICLES, FENCES OR LIKE ENCLOSURES IN GENERAL, e.g. DOORS, WINDOWS, BLINDS, GATES
  • E06B5/00—Doors, windows, or like closures for special purposes; Border constructions therefor
  • E06B5/10—Doors, windows, or like closures for special purposes; Border constructions therefor for protection against air-raid or other war-like action; for other protective purposes
  • E06B5/16—Fireproof doors or similar closures; Adaptations of fixed constructions therefor
  • E06B5/165—Fireproof windows

Definitions

• the present invention relates to fireproof glazing and comprising one or more layers of alkali silicates hydrated between glass sheets. These layers of silicates are as exposed to fire, they form a foam that shields the radiation and keeps the glass sheets even after they are broken under the effect of thermal shock.
• Fire resistant glazings of this type are well known, as well as the performance that is expected. Of these, the most important are of course the ability to withstand the test of fire as long as possible.
• the quality "fireproof” includes the flameproofness, but also the ability to shield the radiation may cause the extension of fire.
• the performances in this field are sensitive to the laminated structure used but also to the composition of the silicate layers used.
• the multiplicity of glass sheets as that of layers is a well-known factor that increases performance.
• the "refractory" nature of the glazing, and its quality of fire resistance, are also a function of the increase in the SiO 2 / M 2 O molar ratio, in which M is one or a mixture of alkali metals.
• the water content, within certain limits, is also a factor that increases the fire resistance.
• Fire resistant glazing must also have optical qualities. Their most frequent use requires that they be transparent. For this property, not only the glazing must offer a good light transmission, but in addition they must have no defects. The latter, considering the manufacturing techniques are for example the presence of bubbles in the silicate, or the formation of a more or less pronounced veil which leads to a more or less important diffusion of the transmitted light. These defects appear either from the constitution of the glazing, or even more to the test of time, and their formation can be accelerated by exposure of the glazing under certain conditions (high temperature, UV irradiation).
• these glazings still include mechanical characteristics. According to their use, for example, these glazings can be used to withstand standardized shocks simulating the impact of a person. These features are again related to the laminated structures chosen, the possible use of interlayer sheets known to improve the mechanical strength of the glazing, such as the presence of PVB sheets, but also the compositions of the alkali silicates used. The fire-resistant glazings are still likely to see their structure itself affected by lack of sufficient stability of the assemblies formed.
• compositions are prepared from solutions of industrial silicates.
• the stability of these solutions limits the dry matter content they contain and this especially as the molar ratio SiO 2 / M 2 O is higher.
• economy of production leads, as far as possible, to limit the drying operations.
• the composition of the final layer results in particular from compromises.
• the starting solution must contain little dry matter. But solutions with a high molar ratio impose a greater drying to reach the final contents which are those of the intumescent layer.
• the refractory nature of the composition is favorable to fire resistance, this character has for counterpart to make the compositions less plastic, and resistance to impact are lessened.
• the plasticity that improves the impact resistance must, however, be well controlled.
• the increase in the water content and hydroxyl compounds which increases this plasticity can lead to a certain structural instability if this content is too important.
• Intumescent products especially if they are in relatively thick layers and in large glazings, may tend to flow under their own weight, leading to deformation of the glazing and improper distribution of the intumescent product.
• the inventors have sought a way to reconcile the different properties of these products, namely simultaneously that they are as effective as possible with respect to their fire resistance, that they offer good mechanical resistance to impact, that they age without disturbing alteration, and whose preparation is organized from abundant products and inexpensive, without requiring too delicate operation.
• the choice of the nature of the silicates was left to the technician.
• the different sources and the very nature of the silicate (s) have apparently been dictated mainly by practical or economic aspects.
• the inventors have shown that the characteristics of the silicates concerned were far from being equivalent in the determination of the properties of the layers.
• the inventors were intended to proceed to the determination of multiple conditions and their interactions for obtaining intumescent products.
• the invention relates to fireproof glazing which, in particular when they contain relatively thick intumescent layers do not lead to deformation due to creep under the effect of their own weight.
• intumescent layers do not lead to deformation due to creep under the effect of their own weight.
• products which otherwise meet the above-mentioned requirements may be unacceptable simply because, being stored vertically for long periods of time, deformation consisting of an increase in thickness in the lower part of the glazing, and a correlative thinning at the top thereof.
• These deformations appear mainly in relatively thick intumescent layers.
• the intumescent layers have a thickness of about one millimeter. At this thickness the evoked creep phenomena are practically not perceptible. It is different when these layers exceed 2mm, especially when the heights are higher.
• the viscosity of the products must be sufficient to ensure the maintenance of the layer without annoying deformation even in glazing large (several meters).
• the viscosity of the intumescent layers according to the invention is at least 0.8. 10 9 Pa ⁇ s, and most preferably at least 1.10 9 Pa.s.
• the viscosity measurement is that made according to ASTM C 1351M-96 under the following conditions of application: a load of 20N
• the intumescent material is caught between two sheets of glass each 3mm thick.
• the layers according to the invention also have a thickness of at least 2.5 mm and preferably at least 3 mm, an SiO 2 / M 2 O molar ratio of 2.5 to 6, and have a water content and hydroxyl compounds of glycerin or ethylene glycol type representing 25 to 45% of the weight of the layer.
• compositions having these viscosities can be arranged in relatively thick layers without leading to a deformation of the glazing by creep.
• potassium is preferred. It gives the layers a particularly favorable refractory character. Lithium can also be present. But its characteristics lead preferably to limit its content. It preferably does not represent more than 10 atomic% of all the alkalis.
• the inventors propose for glazing according to the invention that they comprise intumescent layers with a thickness of at least 2.5 mm and preferably at least 3 mm, always with a water content and hydroxyl compounds of glycerin or ethylene glycol type representing from 25 to 45% of the weight of the layer that they respond to one of the following 11 combinations of conditions between the molar ratio Na 2 O / M 2 O, the weight content of water and compounds hydroxyl (W + H), and the molar ratio R M SiO 2 / M 2 O (M being the sum of Na and K):
• the thicknesses of the layers that can be used can reach or exceed 8mm. Most frequently however the layers in question do not exceed 6mm, and most often not 4mm. In any case, in order for the viscosity to be of significant interest, the intumescent layers must have a thickness of at least 2.5 mm.
• the layers are all the more sensitive to creep as they are thicker. As a result, the viscosity is advantageously higher as the thickness is greater. This is also reflected in the choice of the most appropriate compositions. For very thick layers, it is for example preferred to use a composition in which the sodium content is very high, or a composition containing less water and hydroxyl compounds.
• the silicon / alkali molar ratio is between 2.5 and 6 and preferably from 3 to 6 and particularly preferably from 3.5 to 5.
• the water content in the intumescent layer is between 25 and 45% by weight of the layer, and preferably between 30 and 40% by weight.
• low molecular weight products having hydroxyl functional groups may substitute at least in part for water.
• Advantageously is introduced from 2 to 15% by weight of glycerol or ethylene glycol, and preferably from 4 to 10% by weight.
• the preparation of the compositions used to form these intumescent layers it is advantageous to proceed at least partly by forming the alkali silicate by reaction of alkaline hydroxide and colloidal silica. This preparation as it appears from the prior art allows to combine a high molar ratio and a relatively short drying step.
• silicate solutions with a high molar ratio require a high water content to avoid spontaneous mass increase, the faster the ratio is higher, the composition in question does not need to be preserved. over long periods, and its stability is sufficient and can be further improved if the composition is refrigerated.
• the preparation can combine the use of commercially available alkali silicate solutions and reaction products described above. These properly dosed combinations make it possible, where appropriate, to combine the indicated advantages of a preparation from colloidal silica and alkaline hydroxide, and those related to the low cost of commercially available silicates solutions.
• At least 20% of the silica present is derived from colloidal silica. This proportion is preferably greater than 30% and particularly preferably more than 40%.
• the composition of the layers can still contain various additives in limited proportions. These additives are intended in particular to improve the stability over time of the layers or their mechanical properties, or the interface with the glass sheets.
• the additives when present do not advantageously constitute more than 6% of the weight of the layer.
• the additives used include amino products such as tetramethyl ammonium hydroxide (TMAH), which when present does not represent more than 2% by weight of the layer.
• TMAH tetramethyl ammonium hydroxide
• organosilica compounds especially tetraethyl orthosilicate (TEOS) or methyl-triethoxysilane (MTEOS). These products promote the plasticity of the layers.
• TEOS tetraethyl orthosilicate
• MTEOS methyl-triethoxysilane
• the fireproof glazings comprising the intumescent layers described above are constituted either by casting the composition in a space delimited between two sheets of glass, a seal ensuring the sealing at the periphery of the glazings, or by applying the composition to a horizontal sheet and by partially drying this layer.
• the initial composition is prepared so that it spontaneously leads to a setting more or less rapid mass.
• This setting in mass is possibly accelerated by a moderate heating of the composition.
• An advantage of this method of preparation is not to be dependent on a drying operation more or less long.
• the thickness of the intumescent layers is not limited by the drying time which increases all the more as the layers are thicker. It is about these very thick layers that the absence of creep is particularly important.
• the composition prior to its application to the glass sheet, is brought to a content as low in water as the stability of this composition allows.
• the at least partial use of colloidal silica is particularly recommended.
• the stability of these compositions which must be dried is a function of the content of water and hydroxyl compounds. This stability is ensured when this content is substantially at least equal to 50% by weight of the composition.
• the initial water content is advantageously adjusted by a dehydration operation carried out immediately before the use of the solution.
• Such dehydration is carried out on a solution carried out on a thin layer under vacuum, optionally at a moderate temperature.
• the methods of drying are described in detail in the published application WO 2010/055166.
• the nature of the silicate composition is given by the atomic percentage of sodium in mixed sodium and potassium silicates, the table also compotes the molar ratio R M , the weight content of water in the layer, that of glycerine. (G) and that of TMAH. Finally the table shows the thickness in mm of the layer formed. No. Na% H 2 OG TMAH thickness
• Example 4 The layers formed successfully pass the creep test, with the exception of Example 4 not meeting the characteristics of the invention.
• the creep tendency results from a combination that is too rich in the water and glycerin component that the sodium silicate content does not sufficiently compensate.
• This example is to be compared with Examples 8 or 9 which for a close water content and glycerin, but with an exclusively sodium silicate provide good creep stability.
• the viscosities measured under the conditions indicated above are between 1. 10 9 and 1. 10 10 Pa.s, except for Example 4 for which the viscosity is about 0.6 10 9 Pa.s.

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• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Organic Chemistry (AREA)
• Materials Engineering (AREA)
• Structural Engineering (AREA)
• Inorganic Chemistry (AREA)
• Civil Engineering (AREA)
• Life Sciences & Earth Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Geochemistry & Mineralogy (AREA)
• Joining Of Glass To Other Materials (AREA)
• Laminated Bodies (AREA)
• Paints Or Removers (AREA)
• Fireproofing Substances (AREA)

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• 2010
  • 2010-09-03 BE BE2010/0528A patent/BE1019472A3/fr not_active IP Right Cessation
• 2011
  • 2011-08-31 EP EP11752520.4A patent/EP2611606A2/fr not_active Withdrawn
  • 2011-08-31 US US13/820,013 patent/US20130157036A1/en not_active Abandoned
  • 2011-08-31 CN CN2011800490679A patent/CN103153606A/zh active Pending
  • 2011-08-31 BR BR112013005205A patent/BR112013005205A2/pt not_active Application Discontinuation
  • 2011-08-31 WO PCT/EP2011/064946 patent/WO2012028631A2/fr active Application Filing
  • 2011-08-31 EA EA201390300A patent/EA024543B1/ru not_active IP Right Cessation

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