Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D1/00—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
  • C09D1/02—Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances alkali metal silicates
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B28/00—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
  • C04B28/34—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders
  • C04B28/342—Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing cold phosphate binders the phosphate binder being present in the starting composition as a mixture of free acid and one or more reactive oxides
• • C—CHEMISTRY; METALLURGY
  • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
  • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
  • C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
  • C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
  • C04B2111/00482—Coating or impregnation materials
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
  • Y02W—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
  • Y02W30/00—Technologies for solid waste management
  • Y02W30/50—Reuse, recycling or recovery technologies
  • Y02W30/91—Use of waste materials as fillers for mortars or concrete

Definitions

• the present invention relates to a product coated with at least a coating layer comprising at least one inorganic binder comprising calcium silicate sites connected the one with the other by alumina-silica phosphate bounds with a weight ratio Al 2 O 3 ZSiO 2 comprised between 0.6:1 and 6:1.
• Inorganic phosphate binder of this type is disclosed in WO03/031366 and WO2005/003056, the content of which is incorporated herein by reference.
• a polymeric matrix comprising a binder formed by mixing an alkali metal silicate aqueous solution with a powder comprising silico-aluminous reactive raw materials.
• a polymerization time of more than one hour is however necessary for reaching a sufficient hardening of the matrix.
• an acid solution is prepared by mixing A1 2 O 3 .3H 2 O with phosphoric acid, said acid solution being then mixed with calcium silicate.
• the so obtained binder has after hardening poor mechanical strength.
• the binder used is advantageously the binder as disclosed in WO 03/031366 of Applicant , the content of which is incorporated in the present specification by reference.
• the binder of WO 03/031366 can be sufficiently hardened within a term of less than 10 minutes and which has excellent mechanical properties.
• the binder can be mixed with various fillers.
• WO2005/003056 proposes to use specific filler, especially a combination of specific filler, in order to increase mechanical properties of the mixture binder/filler(s) and/or the final appearance of the composition after its hardening and/or the fire resistance of the composition. For example, it was observed that swelling of the product could be prevented after a water absorption.
• the present invention relates to an improvement of the use of inorganic binder of Applicant previous applications WO 03/031366 and WO 2005/003056, which is characterized by calcium silicate sites which are connected the one with the other by alumina-silica phosphate bonds.
• a problem of the use of inorganic binder as disclosed in WO 03/031366 and WO 2005/003056 is that when making a thin coating layer on a surface of a product, it was difficult to make easily with industrial means coating layer having a quite uniform thickness, especially quite uniform properties.
• the thin coating layer achieved by said spraying of said specific liquid reacting composition had a to face with a reduced number of cavities with a depth of more than 0.1 the average thickness and with a volume of more than 2mm 3 , preferably a reduced number of cavities with a depth of more than 0.1 the average thickness and with a volume of more than lmm 3 .
• the process of the invention was thus suitable for preventing large unevenness' on the top face of the coating, whereby improving the appearance of the product, as well as the mechanical and fire resistance properties of the product.
• the invention relates to a product having at least one face provided on at least a surface of 100cm 2 with at least a coating layer comprising at least one inorganic binder comprising calcium silicate sites connected the one with the other by alumina-silica phosphate bounds with a weight ratio Al 2 O 3 ZSiO 2 comprised between 0.6:1 and 6:1, in which the coating layer has a first face directed towards the product and a second face opposite to said first face, whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the coating layer has a controlled average thickness of less than 3mm, while the second face of said portion has less than 20 cavities, advantageously less than 10 cavities, preferably less than 5 cavities having a depth of more than 0.2 times, advantageously more than 0.1 times the controlled average thickness and with a cavity volume of more than 2mm 3 , advantageously with a cavity volume of more than lmm 3 .
• the coating layer When applied on a surfaces with cavities or pores, the coating layer can act as means for filling the cavities or closing the pores, whereby flattening the top surface of the product.
• the alumina-silica phosphate bounds connecting the calcium silicate sites are advantageously characterized with a SiO 2 /P 2 O 5 molar ratio comprised between 0.1 and 2, preferably 0.2 and 1.5, most preferably between 0.3 and 1.2.
• the coating layer has a substantially uniform thickness, whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 , of the coating layer has a maximum variation of thickness with respect to the average thickness of less than 10% of the average thickness, preferably of less than 5% of the average thickness, most preferably of less than 3% of the average thickness of said portion, and/or whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 , of the coating layer has a substantially flat top face, whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 , of said top face has unevenness 1 of less than 10%, advantageously less than 5%, preferably less than 3% of the average thickness of said portion.
• the calcium silicate containing coating layer has a thickness of less than 2mm, preferably less than lmm, most preferably comprised between 50 ⁇ m and 500 ⁇ m.
• the calcium silicate containing coating layer coats a phosphoric acid resistant layer, advantageously a silicon containing layer, preferably a hydrophobic silicon containing layer.
• the phosphoric acid resistant layer forms a substantially uniform layer with a weight of less than 100g/m 2 , preferably less than 50g/m 2 .
• the calcium silicate containing layer comprises inert fibres with an average (in weight) length of less than 200 ⁇ m, preferably less than lOO ⁇ m, most preferably comprised between 20 and 50 ⁇ m.
• the calcium silicate containing layer comprises less than 50% by weight inert fibres, preferably less than 30% by weight, most preferably comprised between 1 and 25% by weight.
• the fibres are homogeneously dispersed in the calcium silicate containing coating layer.
• the fibre dispersion in the calcium silicate containing coating layer is characterized by an average fibre weight content of the layer per square cm, said average fibre weight content being determined on a surface of 50cm 2 , advantageously of 100cm 2 , preferably of 250cm 2 , most preferably of 500cm 2 or even more, and by a fibre weight content variation per square centimetre for said surface (for which the average weight content has been determined) of less than 10% of the average fibre content, preferably less than 5% of the average fibre weight content.
• the calcium silicate containing coating layer has a weight of less than 2000g/m 2 , advantageously less than 1000g/m 2 , preferably comprised between 100g/m 2 and 750g/m 2 .
• the product provided with the coating is a flexible support with a thickness of less than 5mm, preferably less than 4mm, most preferably less than 3mm, especially less than about 2mm, such as a total thickness comprised between 750 ⁇ m and 1750 ⁇ m.
• the flexible support comprises a flexible mat of fibres and/or a flexible fibres containing fabric, said mat or fabric having a weight of less than 3000g/m 2 , advantageously less than 2000g/m 2 , preferably less than 1000g/m 2 .
• the weight of said mat or fabric is for example comprised between 10g/m 2 and 750g/m 2 , such as 20g/m 2 , 40g/m 2 , 50g/m 2 , lOOg/m 2 , 200g/m 2 , 300g/m 2 and 500g/m 2 .
• the flexible support can also comprises several flexible mat(s) and/or fabric(s), the several mat(s) and/or fabric(s) being advantageously attached the one to the other by the phosphate binder containing layer.
• the flexible mat or fabric comprises glass fibres.
• Other fibres can also be used, provided they are resistant to phosphoric acid and/or provided they are provided with a primer which gives sufficient resistance against phosphoric acid.
• both faces of the flexible support are provided with a calcium silicate containing coating layer.
• the product comprises a first flexible support, a second flexible support, and an intermediate calcium silicate containing layer situated between the first and second flexible layer.
• the first flexible layer is a mat of fibres
• the second flexible layer is a fabric, preferably a woven fabric.
• the mat of fibres has a weight of less than 100g/m 2 , advantageously of less than 50g/m 2 , preferably comprised between lOg/m 2 and 40g/m 2 . The use of such a mat gives to the product a soft touch.
• the product of the invention can also be combined with one or more different elements.
• the product of the invention can be used as support for a foaming element or composition, such as a foaming PUR element or composition. After foaming, the foamed element is rigid.
• the invention relates also to a combined structure comprising a product of the invention and an element attached to or adhered to said product.
• the element comprises advantageously a foamed layer in contact with the product of the invention.
• the foamed layer is preferably a foamed PUR layer with a thickness of at least lcm, advantageously of at least 2cm, such as a thickness comprised between 2.5cm and 10cm.
• the invention relates also to a process for the preparation of a product according to the invention, in which a liquid reacting composition is spayed on at least one surface of the product so as to form a coating layer comprising at least one inorganic binder comprising calcium silicate sites connected the one with the other by alumina-silica phosphate bounds with a weight ratio Al 2 (VSiO 2 comprised between 0.6:1 and 6:1, in which the coating layer has a first face directed towards the product and a second face opposite to said first face, whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the coating layer has a controlled average thickness of less than 3mm, said portion having a second face with less than 20 cavities having a depth of more than 0.2 times the controlled average thickness and with a cavity volume of more than 2mm 3 , whereby said composition comprises :
• the pH of the composition is less than 1, while the solid content of the composition is less than 30% by weight, with the proviso that the weight ratio water/calcium silicate particles is comprised between 0.9 and 2.
• the calcium silicate solid powder of the liquid reacting composition has a weight average particle size lower than 50 ⁇ m, preferably lower than 25 ⁇ m.
• the pH of the composition is preferably less than about 0.5.
• the pH is measured at 2O 0 C.
• the weight ratio water/alumino silica from the alumino silica phosphate is greater than 2.
• the liquid reacting composition comprises inert fibres with an average (in weight) length of less than 200 ⁇ m, preferably less than lOO ⁇ m, most preferably comprised between 20 and 50 ⁇ m.
• the inert fibres of the liquid reacting composition have an average length greater than 1.5 times the weight average particle size of the calcium silicate solid powder.
• the liquid reacting composition comprises less than 20% by weight inert fibres, preferably from 5% to 15%.
• the fibres are homogeneously dispersed in the liquid reacting composition before spraying.
• the spraying of the liquid reacting composition is controlled so as to form a coating with a fibre dispersion characterized by an average fibre weight content of the layer per square cm, said average fibre weight content being determined on a surface of 50cm 2 , and by a fibre weight content variation per square centimeter for said surface of less than 10% of the average fibre content, and/or
• the spraying of the liquid reacting composition is controlled so as to form a coating with a fibre dispersion characterized by an average fibre weight content of the layer per square cm, said average fibre weight content being determined on a surface of 100cm 2 , and by a fibre weight content variation per square centimeter for said surface of less than 10% of the average fibre content, and/or
• the spraying of the liquid reacting composition is controlled so as to form a coating with a fibre dispersion characterized by an average fibre weight content of the layer per square cm, said average fibre weight content being determined on a surface of 250cm 2 , and by a fibre weight content variation per square centimeter for said surface of less than 10% of the average fibre content, and/or
• the spraying of the liquid reacting composition is controlled so as to form a coating with a fibre dispersion characterized by an average fibre weight content of the layer per square cm, said average fibre weight content being determined on a surface of 500cm 2 , and by a fibre weight content variation per square centimeter for said surface of less than 5% of the average fibre content, and/or
• the spraying of the composition is controlled so that at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the second face of the coating layer with a controlled average thickness of less than 3mm, has less than 20 cavities having a depth of more than 0.2 times the controlled average thickness and with a cavity volume of more than lmm 3 , and/or
• the spraying of the composition is controlled so that at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the second face of the coating layer with a controlled average thickness of less than 3mm, has less than 10 cavities having a depth of more than 0.2 times the controlled average thickness and with a cavity volume of more than 2mm 3 , and/or
• the spraying of the composition is controlled so that at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the second face of the coating layer with a controlled average thickness of less than 3mm, has less than 10 cavities having a depth of more than 0.2 times the controlled average thickness and with a cavity volume of more than lmm 3 , and/or
• the spraying of the composition is controlled so that the coating layer has a substantially uniform thickness, whereby at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 , of the coating layer has a maximum variation of thickness with respect to the average thickness of less than 10% of the average thickness, and/or
• the spraying of the composition is controlled so that at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 of the coating layer has a controlled average thickness of less than 3mm,said portion having a maximum variation of thickness with respect to the average thickness of less than 5% of the average thickness, preferably of less than 3% of the average 1 thickness of said portion, and/or
• the spraying of the composition is controlled so that at least a portion of 100cm 2 , advantageously of at least 500cm 2 , preferably of at least 1000cm 2 , of the coating layer has a substantially flat top face having unevenness' of less than 10%, advantageously less than 5%, preferably less than 3% of the average thickness of said portion.
• the surface to be sprayed is treated so as to render it substantially not reactive to phosphoric acid, so as to avoid any excessive foaming due to a reaction between the support and the phosphoric acid of the composition.
• the surface to be coated is precoated with a phosphoric acid resistant layer, such as a hydrophobic phosphoric acid resistant silicon containing layer, preferably a silicon layer, a chloro and/or fluoro silicone layer.
• a phosphoric acid resistant layer such as a hydrophobic phosphoric acid resistant silicon containing layer, preferably a silicon layer, a chloro and/or fluoro silicone layer.
• a layer can be very thin, such as a layer of less than lO ⁇ m.
• the presence of silicon atom in the layer is also advantageous for making chemical bounds between the calcium silicate containing layer and the protection layer against phosphoric acid.
• the coating composition is cured and/or dried at a temperature comprised between 10°C and 75 0 C for at least 30seconds, preferably for a time period comprised between 1 and 5minutes, and/or - at least before spraying the composition, the composition to be sprayed or the portion thereof to be sprayed is heated at a temperature comprised between 30°C and 70°C, and/or
• the liquid composition is sprayed on a face of the product having a temperature comprised between 10°C and 100 0 C, advantageously comprised between 20 0 C and 85 0 C, preferably comprised between 30 0 C and 75°C.
• the drying or curing of the composition is rapid. It has also been observed that the successive spraying of the liquid coating composition was advantageous, so as to apply liquid reactive composition on an already applied coating layer. The successive spraying of the composition is advantageously carried out when the curing or drying of the prior applied composition is not yet finished. On this manner, the newly applied composition is contacting very reactive coating or a coating still in curing reaction, whereby the further curing or hardening of the newly sprayed composition is favorized.
• the calcium silicate containing coating composition is sprayed on a first flexible support resistant to phosphoric acid and/or provided with a phosphoric acid resistant layer, and in which a second flexible support resistant to phosphoric acid and/or provided with a phosphoric acid resistant layer is deposited on the calcium silicate containing coating composition while not being completely cured.
• the coating is applied in at least two successive spraying steps.
• the number of spraying steps will depend of various factors, such as thickness, fibre content, solid content of the liquid composition, etc.
• the number of spraying steps is advantageously at least three, but can be 4, 5, 6, or even more.
• the first and the latest spraying steps are carried out with a composition with a low inert fibre content, advantageously without or substantially without fibres, while the intermediate spraying step(s) is/are carried out with coating composition(s) having a higher inert fibre content.
• the invention further relates to a liquid reacting composition suitable to be sprayed, said composition comprising : - an aqueous alumina-silica phosphate solution with an Al 2 O 3 /SiO 2 weight ratio comprised between 0.6 and 6 and a SiO 2 /P 2 O 5 molar comprised between 0.1 and 2, preferably 0.2 and 1.5, most preferably between 0.3 and 1.2,
• the pH of the composition is less than 1, preferably less tan 0.5, while the solid content of the composition is less than 30% by weight, with the proviso that the weight ratio water/calcium silicate particles is comprised between 0.9 and 2.
• the weight average particle size of the calcium silicate solid powder is lower than 50 ⁇ m, preferably lower than 25 ⁇ m.
• the weight ratio water/alumino silica from the alumino silica phosphate is greater than 2.
• the composition comprises inert fibres (i.e. inert fibres means fibres not soluble in the acid composition, namely in the phosphoric acid composition during the hardening or curing of the coating composition) with an average (in weight) length of less than 200 ⁇ m, preferably less than lOO ⁇ m, most preferably comprised between 20 and 50 ⁇ m.
• inert fibres means fibres not soluble in the acid composition, namely in the phosphoric acid composition during the hardening or curing of the coating composition
• average (in weight) length of less than 200 ⁇ m, preferably less than lOO ⁇ m, most preferably comprised between 20 and 50 ⁇ m.
• the inert fibres have an average length greater than 1.5 times the weight average particle size of the calcium silicate solid powder.
• the liquid reacting composition comprises less than 20% by weight inert fibres, most preferably from 1% to 15%, especially from 5 to 15% by weight.
• the invention still further- relates to a product comprising :
• the intermediate layer comprises at least one inorganic binder comprising calcium silicate sites connected the one with the other by alumina-silica phosphate bounds with a weight ratio Al 2 (VSiO 2 comprised between 0.6:1 and 6:1.
• the alumina-silica phosphate bounds connecting the calcium silicate sites are advantageously characterized with a SiO 2 /P 2 O 5 molar ratio comprised between 0.1 and 2, preferably 0.2 and 1.5, most preferably between 0.3 and 1.2.
• the support is a flexible support.
• the intermediate layer forms bounds between support and the mat of fibres.
• the support is resistant to phosphoric acid or provided with a phosphoric acid resistant layer, and in which the mat of fibres is resistant to phosphoric acid or provided with a phosphoric acid resistant layer.
• the support is a flexible fabric, preferably a woven flexible fabric, said fabric having advantageously a weight of less than lOOOg/m 2 , preferably less than 500g/m 2 .
• the mat of fibres has a weight of less than lOOg/m 2 , advantageously of less than 50g/m 2 , preferably comprised between 10g/m 2 and 40g/m 2 .
• the intermediate layer has a thickness of less than 3mm, advantageously less than 2mm, especially less than lmm, most specifically between 50 ⁇ m and 750 ⁇ m.
• the intermediate layer is advantageously made by using a composition of the invention, especially by spaying the composition on the support, and then by covering the sprayed coating layer with the mat of fibres.
• the invention further relates to a metal support or sheet (such as a steel support or sheet) covered at least partly with a resin foam layer, especially with a PUR foam layer, whereby said metal support is provided with a coating layer intermediate at least partly between the metal support or sheet and the resin foam layer, said intermediate layer, said intermediate layer comprising at least one inorganic binder comprising calcium silicate sites connected the one with the other by alumina- silica phosphate bounds with a weight ratio Al 2 O 3 ZSiO 2 comprised between 0.6:1 and 6:1, whereby said layer has an average thickness of less than 3mm, advantageously of less than 2mm, preferably less than lmm.
• the intermediate layer is a coating layer having one or more characteristics of the coating layer of a product of the invention as disclosed here above.
• the alumina-silica phosphate bounds connecting the calcium silicate sites are advantageously characterized with a SiO 2 /P 2 O 5 molar ratio comprised between 0.1 and 2, preferably 0.2 and 1.5, most preferably between 0.3 and 1.2.
• the intermediate layer is a product of the invention as disclosed here above, said product being provided on its both faces with a coating layer.
• a product comprises advantageously a flexible support, such as a flexible fabric and/or mat.
• Figure 1 is a perspective view of foamed support provided with a calcium silicate containing coating of the invention
• Figure 2 is a partial enlarged view, in cross section, of the coating of the support of
• Figure 1 while figure 2bis is an enlarged view of a product not of the invention
• Figure 3 is a perspective view of a flexible product of the invention.
• Figure 4 is an enlarged cross section view of the flexible product of Figure 3;
• Figure 5 is a perspective view of a further flexible product of the invention
• Figure 6 is an enlarged cross section view of the flexible product of Figure 5;
• Figure 7 is a perspective view of another product of the invention.
• Figure 8 is a partial enlarged cross section view of the product of Figure 7;
• Figure 9 is a partial enlarged cross section view of a product similar to the product of figure 4;
• Figures 10,11,12, 13 and 14 is a partial enlarged cross section view of product respectively similar to the product shown in Figures 2, 4,6 and 8;
• Figure 15 is a schematic view of a plant for the production of a product of the invention.
• Figure 1 is a schematic view of a product of the invention.
• the product comprise a foamed support 1, for example a PUR foam with closed cells, and a top coating layer 2.
• the top coating layer 2 comprises :
• an inorganic binder comprising calcium silicate sites connected the one to the other by alumina-silica phosphate bounds having a weight ratio Al 2 O 3 /SiO 2 comprised between 0.6:1 and 6:1, and
• the coating layer was prepared by spraying in one or preferably successive steps a liquid reactive composition comprising :
• the average length of the fibres being at least 2 times the average maximum length of the calcium silicate solid powder, whereby the pH of the composition is less than about 0.5, while the solid content of the composition is less than 30% by weight, with the proviso that the weight ratio water/calcium silicate particles is comprised between 0.9 and 2.
• the sprayed composition comprises less than 20% by weight inert fibres, preferably from 5% to 15%.
• the liquid reactive composition was sprayed so as to achieve after hardening and drying of the composition a coating layer 2 having a thickness E of less than 2mm, such as 1.5mm, lmm, 750 ⁇ m, 500 ⁇ m and 250 ⁇ m.
• the upper face 20 of the coating layer 2 i.e. the face opposite to the face 21 facing the support 1 , has substantially no cavities, while the fibres are quite homogeneously distributed with respect to the surface of the coating.
• top coating face 20 having less than 5 cavities with a depth greater than 0.1 times the thickness of the coating 2 and with a cavity volume of more than 2mm 3 , for a top coating surface of 2000 cm 2 .
• the liquid reactive composition was prepared by using the following products : WATER W : demineralized water with a very low calcium/magnesium content (less than 20 ⁇ pm)
• SiO 2 precipitated SiO 2 particles with an average particle size of about lO ⁇ m, said particles having a purity of 99% by weight
• Al 2 O 3 powder with an average particle size of about lO ⁇ m and a purity of 99% by weight
• Phosphoric acid PA concentrated phosphoric acid, as an aqueous solution containing 75% by weight phosphoric acid
• Calcium silicate CSl calcium meta silicate powder, water insoluble, acicular nature with a length/breadth or aspect ratio of about 3 to 5, advantageously about 3 , with an average weight particle of about 15 ⁇ m.
• the calcium silicate comprises more than about 46% (weight) CaO and more than about 51.5% (weight) (calculated after burning).
• Calcium silicate CS2 calcium meta silicate powder, water insoluble, acicular nature with a length/breadth or aspect ratio of about 3 to 5, advantageously about 3, with an average weight particle of about lO ⁇ m.
• the calcium silicate comprises more than about 46% (weight) CaO and more than about 51.5% (weight) (calculated afterburning).
• Calcium silicate CS3 calcium meta silicate powder, water insoluble, acicular nature with a length/breadth or aspect ratio of about 3 to 5, advantageously about 3, with an average weight particle of about 5 ⁇ m.
• the calcium silicate comprises more than about 46% (weight) CaO and more than about 51.5% (weight) (calculated after burning).
• Calcium silicate CS4 calcium meta silicate powder, water insoluble, acicular nature with a length/breadth or aspect ratio of about 3 to 5, advantageously about 3, with an average weight particle of about 2.5 ⁇ m.
• the calcium silicate comprises more than about 46% (weight) CaO and more than about 51.5% (weight) (calculated after burning).
• Glass fibre (GFl) glass fibre with a length of about 50 ⁇ m, said fibre being treated with a water repellent silane layer (fluoro silane layer)
• Glass fibre (GF2) glass fibre with a length of about 25 ⁇ m, said fibre being treated with a water repellent silane layer (fluoro silane layer)
• Silica fume (Sf) average particle size (in weight) below 1 ⁇ m.
• the binder composition have been prepared by adding SiO2 particles to phosphoric acid. After dissolution of the SiO2 particles, A12O3 particles were added. An acid alumina silica phosphate aqueous solution was so achieved. The pH of said acid solution, measured at 20°C was less than about 0.5.
• some "inert” fillers were added, namely glass fibres and/or silica fume.
• Water can be further be added, but the pH is preferably maintained below 1. It has been observed that when keeping the pH below 1, the fluidity of the composition can be ensured even if the composition has a solid content of about 30% by weight, whereby ensuring an efficient spraying of the composition with normal industrial spraying system. It was also observed that the mixing of the suspension was more easy at such a low pH, and that the composition could be easily kept sufficiently homogeneous, even without mixing or shaking for a time sufficient for the spraying.
• compositions 1 to 16 were sprayed on a foamed support (PUR) in several spraying steps for achieving different coating layers, namely coating layers having different thickness, namely 2mm, lmm, 750 ⁇ m, 500 ⁇ m and 250 ⁇ m.
• the variation of thickness was very low, namely a variation of less than 2% with respect to the average thickness.
• the fibres were well distributed, due to the easiness to keep the suspension homogeneous and due to the possibility to apply the suspension by spraying.
• the variation of fibre content per cm 2 is less than 3% of the average (weight) fibre content determined for a coating surface of 1000cm 2 . It was even observed that it was possible to have fibres directed in substantially all the planar directions, whereby ensuring good mechanical properties for the coating as such in any planar direction.
• the support provided with a wet coating was placed in a oven at 50 0 C for 1 minute. After said drying, the coating 2 was hardened and well attached to the support.
• the coating composition 2 of the invention has properties which are quite constant.
• the liquid suspension binder compositions 1, 2, 6 and 7 of WO 2005/003056 were used for coating a support.
• the coating of the support could not be achieved by spraying.
• the top face (see figure 2 bis) had cavities 201 and/or asperities or projections. Some cracks were apparent.
• the coating had thus many cavities (more than 20 cavities with a depth "d" greater than 0.2 times the thickness of the coating 200).
• WO 2005/003056 suggests the addition of silicon containing fibres with a length advantageously comprised between 25 ⁇ m and 300 ⁇ m Such a composition can still no be sprayed with efficient spraying industrial system. Very thin layer without asperities and/or cavities and/or grooves can not be achieved.
• Figure 2 bis shows schematically a coating layer 200 prepared from a liquid binder composition with fibres. The coating layer had some variation of properties due to variation of thickness, as well as variation in the fibre density. Moreover, still some cavities were present along the top surface of the coating 200.
• Figure 3 shows a fabric which was coated with compositions of Tables 1 and 2. The fabric 30 is for example a glass fabric with a weight comprised between 200g/m 2 and 500g/m 2 .
• the woven glass fabric was coated by several successive spraying steps, so that the top face was substantially flat.
• compositions 1 to 16 as disclosed for the embodiment of figure 1 are used for the coating.
• the coating was carried out only on one face of the fabric.
• the thickness of the coating 2 was advantageously less than 750 ⁇ m, such as 500 ⁇ m, 300 ⁇ m, 200 ⁇ m, lOO ⁇ m, or even lower, so as to keep the coated woven glass fabric still sufficiently flexible.
• the coated fabric passes advantageously at least 15 seconds (for example between 20 and 50 seconds) in an oven at a temperature comprised between 40 and 80°C. Possibly, a flash drying can be operated at a higher temperature.
• the coating can be carried out substantially continuously.
• the fabric from a roll is unrolled, before passing in front of one or more spraying stations or ramps.
• the fabric passes through an oven so as to ensure a sufficient hardening of the coating.
• the dried coated fabric is then rolled back into a roll.
• the so coated fabric is still sufficient flexible for being rolled back.
• a mandrel having a minimum diameter of 20cm (preferably at least 25cm, such as 30cm) for the rolling up of the coated fabric.
• the so rolled coated fabric can then be protected by a plastic or paper film or sheet.
• the fabric is advantageously a glass woven fabric, having a weight comprised between lOOg/m 2 and 1500g/m 2 , preferably between 100g/m 2 and 750g/m 2 .
• Figure 5 is a schematic view of a coated fabric similar to the coated fabric of figure 3, except that both faces of the fabric have been coated with a coating layer 2A and 2B.
• the thickness of the coating layers 2A, 2B can be identical or different, but advantageously lower than 2mm, preferably lower than 1.5mm.
• Preferably the total thickness of the coated fabric is less than about 2mm, such as less than about 1.5mm.
• the outer coating layer or the layer intended to be directed outwardly is thicker than the inner layer.
• the inner layer can possibly be very thin, such as less than lOO ⁇ m.
• the method for manufacturing such a coated fabric is for example as follows :
• the fabric 30 from a roll is unrolled, before passing in front of one or more spraying stations or ramps, so as to coat one face of the fabric. After said face being coated, the fabric passes through an oven so as to ensure a sufficient hardening of the coating layer.
• compositions 1 to 16 as disclosed for the embodiment of figure 1 are used for the coating.
• the fabric is advantageously a glass woven fabric, having a weight comprised between lOOg/m 2 and 1500g/m 2 , preferably between 100g/m 2 and 750g/m 2 .
• the downwards face is now the upwards face of the fabric.
• the now upwards face passes in front of one or more spraying station or ramps, so as to coat said face.
• Said coated face passes then in an oven for ensuring a sufficient hardening of the coating.
• the dried coated fabric is then rolled back into a roll.
• the so coated fabric is still sufficient flexible for being rolled back.
• a mandrel having a minimum diameter of 20cm (preferably at least 25cm, such as 30cm) for the rolling up of the coated fabric.
• the so rolled coated fabric can then be protected by a plastic or paper film or sheet.
• Figure 7 is a schematic view of a further product of the invention.
• Said product comprises a fabric 30 which is coated with a coating layer 2, which is covered by a mat of fibres 32.
• the coating forms here at least an intermediate layer extending between the fabric and the mat. A portion of the coating extend within the fabric and within the mat.
• compositions 1 to 16 as disclosed for the embodiment of figure 1 are used for the coating.
• the mat 32 is deposited on the coating layer before it hardening, and is advantageously pressed in the coating. Thereafter, the product passes in an oven (for example having a temperature of 6O 0 C) for less than 1 minute, so as to harden very quickly the coating composition.
• an oven for example having a temperature of 6O 0 C
• the fabric is advantageously a glass woven fabric, having a weight comprised between lOOg/m 2 and 1500g/m 2 , preferably between lOOg/m 2 and 750g/m 2 .
• the mat 32 is advantageously a mat with a weight of less than 200g/m 2 , preferably between lOg/m 2 and 150g/m 2 , especially between 20g/m 2 and 50g/m 2 .
• Such a product can be manufactured as follows.
• the fabric 30 is unrolled from a roll and is moved towards a spray station or spray ramp(s).
• a mat is unrolled from a roll and is moved towards the coated fabric.
• the mat is then pressed towards the coated fabric, whereby coating enters at least partly in the openings of the mat.
• the coated fabric provided with the mat is then heat dried so as to ensure a quick hardening of the coating.
• the product, after its hardening is rolled back on a mandrel.
• the coating and the mat can pass between one or more heated rollers, said rollers being adapted for ensuring a hardening of the coating, as well as a compression of the structure. This enables a better adhesion of the mat with the fabric.
• Figure 9 is a view of a product similar to that of figure 4, except that the top face 20 of the coating is provided with a protection film or layer 33, such as a very thin water repellent layer.
• a water repellent layer can be a fluoro silane layer (such as the product Cascada ® ), Such a water repellent layer can be very thin.
• compositions 1 to 16 as disclosed for the embodiment of figure 1 are used for the coating.
• Figures 10, 11, 12, 13 and 14 are view of embodiments respectively similar to the embodiments of figure 2, 4, 6, 8 and still 8.
• the support 1 to be coated is protected by an intermediate layer 40 resisting to phosphoric acid, said layer containing advantageously one or more silicon atoms.
• the woven fabric 30 is first coated with a protection layer 40, said layer covering only one face of the fabric.
• a protection layer 40 can be very thin, such as a layer with a thickness of less than lOO ⁇ m.
• a protection layer is advantageously a silane layer.
• a liquid aqueous acid alumina-silica phosphate composition containing solid calcium silicate is deposited on the protection layer 40.
• the flexible coated fabric can be rolled up on a mandrel.
• the inorganic binder containing layer had for example a thickness of 100 ⁇ m to 2000 ⁇ m.
• the fabric is provided on its both faces with a protection layer
• the fabric 30 is provided on its both faces with an acid protection layer 40A,40B.
• An inorganic binder containing layer 2 is deposited on one of the protected face of the fabric. While still not completely hardened, a mat of fibres 32 is placed on the coating layer and pressed thereon. The mat is prepared from fibres resistant to phosphoric acid.
• the woven fabric 30 and the mat 32 are prepared from fibres resistant to phosphoric acid.
• Figure 15 is a schematic of an installation for preparing continuously or substantially continuously product provided with an inorganic binder containing layer.
• the installation of figure 15 comprises :
• - means for placing the product to be coated in line 100 such means being for example a means for unrolling a roll 101 of a product, such as a roll of a fabric or mat or combination thereof;
• a means 102 for providing at least one face, or both faces of the product with a phosphoric acid resistant layer is for example a system with one or more spraying means 103 for providing one or both faces with a protection layer, and a dryer unit 104;
• a coating unit 105 for providing at least one face of the product with a liquid reactive coating composition comprising an aqueous alumina-silica phosphate solution, calcium silicate and possibly one or more inert fillers, said coating unit 105 comprising advantageously one or more spraying system 106;
• a dryer 109 for hardening the composition for example said dryer being an oven 110 (with heating system for reaching a temperature comprised between 40°C and 90°C) and/or heating roller(s), especially in the case a further product has to be pressed against the product ;
• a rolling system 111 for rolling up the coated product on a mandrel possibly a rolling system 111 for rolling up the coated product on a mandrel, or a foaming unit 112 in which a foaming composition is deposited on the face of the support not provided with the coating layer or provided with a coating layer, so as to form a foamed layer attached to the coated product.
• Metal supports not galvanized, such as steel supports, iron supports, etc. have been spray coated with compositions disclosed for the product of Figure 1.
• the metal supports were beams, I-beams, plates with thickness of lmm, 2mm, 5 mm, and 10mm.
• the coated supports were air dried with heated air wit a temperature of 45 0 C to 80 0 C.
• the coating layer had a thickness of less than lmm, such as a thickness of lOO ⁇ m, 200 ⁇ m, 300 ⁇ m, 500 ⁇ m and 750 ⁇ m.
• the coated face of the products was resistant to corrosion, by the alumino-silicate layer as such, but also by the formation of some phosphate layer forming a kind of intermediate layer between the face of the product and the alumino silicate layer.
• the so coated metal sheets or supports have then been provided with a resin foam layer, such as a PUR foam layer. It has been observed that the adhesion of the foam PUR layer on the coating layer was excellent and much better than the simple direct coating of the metal sheet with the foam PUR layer.

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