WO2004014815A1 - Lösemittelfreies verfahren zur hydrophoben farbbeschichtung von glasgranulat, das produkt hieraus und seine verwendung - Google Patents
Lösemittelfreies verfahren zur hydrophoben farbbeschichtung von glasgranulat, das produkt hieraus und seine verwendung Download PDFInfo
- Publication number
- WO2004014815A1 WO2004014815A1 PCT/DE2003/002319 DE0302319W WO2004014815A1 WO 2004014815 A1 WO2004014815 A1 WO 2004014815A1 DE 0302319 W DE0302319 W DE 0302319W WO 2004014815 A1 WO2004014815 A1 WO 2004014815A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- color
- glass
- coated
- glass granules
- solvent
- Prior art date
Links
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
- C03C17/006—Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
- C03C17/008—Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character comprising a mixture of materials covered by two or more of the groups C03C17/02, C03C17/06, C03C17/22 and C03C17/28
- C03C17/009—Mixtures of organic and inorganic materials, e.g. ormosils and ormocers
-
- 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
- C03C1/00—Ingredients generally applicable to manufacture of glasses, glazes, or vitreous enamels
- C03C1/002—Use of waste materials, e.g. slags
-
- 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
- C03C12/00—Powdered glass; Bead compositions
-
- 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
- C03C17/006—Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character
- C03C17/007—Surface treatment of glass, not in the form of fibres or filaments, by coating with materials of composite character containing a dispersed phase, e.g. particles, fibres or flakes, in a continuous phase
-
- 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
- C04B14/00—Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
- C04B14/02—Granular materials, e.g. microballoons
- C04B14/04—Silica-rich materials; Silicates
- C04B14/22—Glass ; Devitrified glass
-
- 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
- C04B26/00—Compositions of mortars, concrete or artificial stone, containing only organic binders, e.g. polymer or resin concrete
- C04B26/02—Macromolecular compounds
-
- 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
- C03C2217/00—Coatings on glass
- C03C2217/40—Coatings comprising at least one inhomogeneous layer
- C03C2217/43—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
- C03C2217/44—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the composition of the continuous phase
- C03C2217/445—Organic continuous phases
-
- 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
- C03C2217/00—Coatings on glass
- C03C2217/40—Coatings comprising at least one inhomogeneous layer
- C03C2217/43—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
- C03C2217/46—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
- C03C2217/47—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase consisting of a specific material
- C03C2217/475—Inorganic materials
-
- 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
- C03C2217/00—Coatings on glass
- C03C2217/40—Coatings comprising at least one inhomogeneous layer
- C03C2217/43—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase
- C03C2217/46—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase
- C03C2217/48—Coatings comprising at least one inhomogeneous layer consisting of a dispersed phase in a continuous phase characterized by the dispersed phase having a specific function
- C03C2217/485—Pigments
-
- 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
- C03C2217/00—Coatings on glass
- C03C2217/70—Properties of coatings
- C03C2217/72—Decorative coatings
Definitions
- the invention relates to a solvent-free process for producing hydrophobic color-coated glass (preferably recycled glass) granules, the hydrophobic or superhydrophobic color-coated glass granules produced by this process as products thereof and the use of these products.
- An essential motive for the present invention was the recognition that for the coloring of an opaque, ie non-transparent mineral grain significantly more color pigment - and thus color pigment-binding binder - is needed than for the coloring of a transparent grain of glass:
- a superficially dyed Non-transparent quartz grain is only visually appealing to the surface of the viewer, but not to the back surface, since the color pigments adhering to the back are removed from the visual perception by the opacity of the grain.
- the color pigments applied all over add up to the overall color impression, since, especially with a very thin and thus slightly translucent color coating, the color pigments applied to the back are optically perceived.
- the process should be single-layered, i. do not require adhesion-promoting priming of the glass granules.
- the method should be feasible with the least possible expenditure of energy, in particular thermal energy. This is especially true for the required to dry the paint coat hot air effect.
- the complete dehumidification should take place at the lowest possible hot air temperature and the shortest possible exposure to warm air.
- the colored coating should not only be non-hygroscopic, ie absorb moisture from the ambient air. It should not only be waterproof, ie in an aqueous environment do not dissolve or swell or absorb water in appreciable amount. But it should also repel water, ie its surface is a clearly hydrophobic
- the colored coating should permanently adhere firmly to the glass grain, even with high fluctuations in the ambient temperature - z. In the range between -25 ° C and + 85 ° C. 3.
- the colored coating should have a high abrasion resistance, so that it does not dust or bleed even under possibly high mechanical stress by compulsory mixing processes in the course of further processing of the color-coated glass granules. 4.
- the colored coating should have a good chemical resistance, d. H. the colored coated glass granules should be diluted with diluted alkalis and
- Acids, salts and aggressive organic substances (such as monostyrene or methyl methacrylate), which could act on the granules during further processing to final products or in the application of the final products, be sufficiently resistant.
- solvent-based synthetic resins include solvent-based epoxy or polyurethane systems as well as reaction resin systems such as unsaturated polyester resins or Polymethylmethacrylatharze containing in the unpolymerized state evaporative, usually foul-smelling and hazardous to health substances such as monomeric styrene or methyl methacrylate or release them in the course of the polymerization.
- water glass is hygroscopic and water-soluble
- mixtures of water glass and aqueous acrylate dispersions are likewise hygroscopic or water-absorptive.
- pigment-filled aqueous acrylate dispersions are less susceptible to moisture after they have cured. Coated surfaces tend to swell only after prolonged exposure to moisture. As a glass coating, however, they have no optimal adhesion to the glass and thus also no high abrasion resistance.
- WO 01/14277 describes surface-finished concrete blocks which are provided with a polymer artificial stone layer. This finishing layer contains, as appearance-determining main filler, waste glass granules which are produced by means of an aqueous dispersion of polyvinyl acetate and
- Aqueous polyvinyl acetate dispersions - whether dyed or undyed - are slightly hygroscopic after drying. They swell when exposed to water, the surface of the coating is not hydrophobic. In addition, they react saponifying to alkaline influences and are sensitive to many aggressive organic substances such. For example, methyl methacrylate.
- aqueous two-part epoxy resin systems reaction-curing epoxy resin systems in which at least one of the two solvent-free components-the parent component or the hardener component-is dispersed or emulsified in water so that the solvent-free epoxy resin system can be diluted with water and / or solvent-free aqueous additives. It has been found that all the requirements described above, which are imposed on the product to be produced according to the invention, are fulfilled by producing the product - color-coated (recycled) glass granules having a hydrophobic surface - by the same process.
- Resin systems were additionally diluted with up to 30% by weight of water prior to use and filled with up to 100% by weight of colored pigment (preferably inorganic mineral pigment). It has been found that glass granules coated with such a water-diluted and pigment-filled resin system dehumidify completely with little use of thermal energy (eg at a hot air temperature of 60-80 ° C.) in a very short time (eg up to 90 seconds) to let.
- the color-coated glass granules are dust-dry and non-sticky after cooling, so that the time-dependent reactive curing of the resin system in a storage vessel at ambient air temperatures> 10 ° C can take place without supply of thermal energy.
- the color coating of the granules after reaching the final strength not only has a strong adhesion and abrasion resistance but also a high chemical resistance and especially a clearly hydrophobic property of the surface. It has been found that the hydrophobic surface property of the color-coated glass grains according to the invention can be increased to a "superhydrophobic" property by enriching the described color coating with siloxane molecules:
- the solvent-free, aqueous, two-component and pigment-filled epoxy resin system is not diluted with water but with a very low-viscosity, siloxane-containing aqueous emulsion, for example, an aqueous methylalkylsiloxane / acrylic acid ester copolymer
- siloxane molecules bind to those contained in the coating mixture
- Mineral pigments For dyeing, no mineral pigments but e.g. organic pigments used, it is necessary that the mixture feinst- granular, as colorless as possible, powder of mineral origin, for. As glass and / or aluminum hydroxide and / or natural or synthetic mica is added so that the siloxane molecules find a binding partner. When using aluminum hydroxide, there are advantages in terms of the fire behavior of the coating: the flammability is reduced, self-extinguishing is favored.
- the binder is mixed not only mineral color pigment and / or mineral fine filler of glass and / or aluminum hydroxide and / or mica but also metallic pigment -.
- Aluminum powder - or fine platelets made of - uncoated or epoxy-coated - aluminum foil.
- metallic pigment gives the coated granules a metallic luster comparable to that of electrically oxidised aluminum.
- the color-coated glass granules according to the invention are primarily suitable for use as appearance-determining main additives for plaster or screeds bound in organic or inorganic form, as well as for moldings and facing layers made of polymer concrete or granite-like structured polymer artificial stone.
- such end products should also be suitable for outdoor use exposed to the weather.
- the color-coated glass granules are processed into granite-structured end products whose microstructure is interspersed with fine capillary pores. This can be done, for example, if a very "lean", ie low-binder polymer mortar was not compacted with sufficient pressure or if the grading curve of the aggregates has too small a proportion of fine filler.
- the granules were mixed with the liquid colorant.
- the mixing time was 60 seconds.
- the coated granules were dehydrated.
- the temperature of the air stream was 60 ° C.
- a complete dehumidification was achieved after 80 seconds.
- the color-coated glass granules were dust-dry.
- the coated granules were dehydrated.
- Temperature of the air flow was 60 ° C. A complete dehumidification was achieved after 80 seconds.
- the color-coated glass granules were dust-dry.
- aqueous polyamine-epoxy resin adduct were stirred with 45 ml of a very low-viscosity aqueous methylalkylsiloxane / acrylic acid ester copolymer emulsion and 140 g of mineral ultramarine color pigment. Then, 66 g of the second resin component - a mixture of bisphenol A-epichlorohydrin resin, p-tert-butylphenyl glycidyl ether and benzyl alcohol - was homogeneously stirred.
- the recycled glass granules were coated with the colorant.
- the mixing time was 60 seconds.
- the coated granules were dehydrated.
- the hot air temperature was 80 ° C, the warm air exposure time was 120 seconds.
- Each 20 kg of colorless transparent recycled glass granules in grain sizes of 0.8 to 1.2 mm should be hydrophobically color-coated in a slightly translucent ultramarine-blue shade with a partial reflective effect.
- 2 different aqueous hardener components of the epoxy resin system should be used.
- the hardener-pigment mixtures were then each mixed with 90 g of a viscosity-reduced, reactive-dilute bisphenol A resin with simultaneous stirring of 150 g of fine platelets of epoxy-coated aluminum foil in the format 600 ⁇ m ⁇ 600 ⁇ m ⁇ 5-10 ⁇ m. After about 40 minutes, the Glasgranulatchargen were each coated with one of these mixtures in the plowshare mixer. The mixing time was 60 seconds.
- the coated granule batches were dehydrated.
- the temperature of the air stream was 85 ° C.
- a complete dehumidification was achieved after about 120 seconds.
- the aluminum flakes adhered to the glass grain surfaces with sufficient strength.
- both color-coated glass granules were dust-dry. They were filled into sacks and stored at about 20 ° C. In both cases, the hydrophobic and partially mirrored color coat had reached its final strength after about 3 days by reactive curing
- test was carried out according to the test method described on page 9, lines 16-31, ie in each case 60 g of test material were mixed with 20 g of siloxanized glass powder each time.
- the addition of the siloxanized (and thus hydrophobic) glass powder was made with the aim of delaying the sinking of the water into the agglomerate to allow a more precise observation.
- the experiments were carried out several times. The results given here represent average values.
- EXAMPLE 2 a In order to obtain comparative values, granules were first tested which do not correspond to the present invention and do not expect a hydrophobic surface property.
- the mean sinking time (t) was more than 48 hours. The experiments were stopped after 48 hours, as it became clear that the water evaporates faster than seepage.
- the color-coated recycling glass granules produced by the process according to the invention can be used in many ways as an additive for organically or inorganically bound mortars, plaster mortars and screeds as well as for molded articles and coatings of polymer concrete or granite-like structured polymer artificial stone. Due to their hydrophobic property, they are particularly suitable for weather-stressed building materials or components such as e.g.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003254624A AU2003254624A1 (en) | 2002-07-12 | 2003-07-10 | Solvent-free method for hydrophobic color coating of glass granulates, product therefrom and use thereof |
DE10393341T DE10393341D2 (de) | 2002-07-12 | 2003-07-10 | Lösemittelfreies Verfahren zur hydrophoben Farbbeschichtung von Glasgranulat, das Produkt hieraus und seine Verwendung |
EP03783916A EP1523457A1 (de) | 2002-07-12 | 2003-07-10 | Lösemittelfreies verfahren zur hydrophoben farbbeschichtung von glasgranulat, das hieraus resultierende produkt und seine verwendung |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10231858A DE10231858A1 (de) | 2002-07-12 | 2002-07-12 | Lösemittelfreies Verfahren zur hydrophoben Farbbeschichtung von Glasgranulat |
DE10231858.1 | 2002-07-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004014815A1 true WO2004014815A1 (de) | 2004-02-19 |
Family
ID=29761956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DE2003/002319 WO2004014815A1 (de) | 2002-07-12 | 2003-07-10 | Lösemittelfreies verfahren zur hydrophoben farbbeschichtung von glasgranulat, das produkt hieraus und seine verwendung |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1523457A1 (de) |
AU (1) | AU2003254624A1 (de) |
DE (2) | DE10231858A1 (de) |
WO (1) | WO2004014815A1 (de) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE202009013082U1 (de) | 2009-10-01 | 2010-02-25 | Schultze-Kraft, Andreas | Trivalent beschichtetes Glasgranulat als Betonzuschlag |
JP2014501344A (ja) * | 2010-12-29 | 2014-01-20 | ビーエーエスエフ ソシエタス・ヨーロピア | 着色複合舗装構造 |
RU2565671C1 (ru) * | 2014-05-30 | 2015-10-20 | Федеральное государственное бюджетное учреждение науки Институт синтетических полимерных материалов им. Н.С. Ениколопова Российской академии наук (ИСПМ РАН) | Разветвленные фторсодержащие кремнийорганические сополимеры, способ их получения и гидрофобное полимерное покрытие на их основе |
US9464003B2 (en) | 2009-06-24 | 2016-10-11 | Basf Se | Method of producing a composite material using a mixing system |
US9505931B2 (en) | 2009-12-21 | 2016-11-29 | Basf Se | Composite pavement structure |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2142487A1 (de) * | 2007-05-04 | 2010-01-13 | E. I. Du Pont de Nemours and Company | Beschichtete und schimmernde partikel sowie industriestein damit |
DE102009043662B4 (de) * | 2009-09-29 | 2013-07-04 | Andreas Schultze-Kraft | Partiell lichtdurchlässige zementös oder polymer gebundene Werksteinplatten |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1604405A (en) * | 1978-05-31 | 1981-12-09 | Univ Cardiff | Articles made from resin compositions containing aggregate materials eg glass |
WO1989011457A1 (en) * | 1988-05-27 | 1989-11-30 | Schultze Kraft Andreas | Process for producing artificial stones, and their use |
DE4334623A1 (de) * | 1993-10-06 | 1995-04-13 | Grundstuecks Verwaltung Frenze | Behandlung von Glasbruch als Zuschlagstoff in Mineralstoffgemischen |
DE4402432A1 (de) * | 1994-01-27 | 1995-08-03 | Schultze Kraft Andreas | Oberflächenbeschichtete Granulate und Formteile für die Herstellung von Formteilen aus Polymerkunststein und Polymerbeton |
WO2001007528A1 (en) * | 1999-07-22 | 2001-02-01 | Ppg Industries Ohio, Inc. | Pigmented coatings for ceramic substrates |
WO2002076904A2 (de) * | 2001-03-27 | 2002-10-03 | Pur-Bauchemie Gmbh | Glashaltiger baustoffkörper oder -belag |
-
2002
- 2002-07-12 DE DE10231858A patent/DE10231858A1/de not_active Withdrawn
-
2003
- 2003-07-10 EP EP03783916A patent/EP1523457A1/de not_active Withdrawn
- 2003-07-10 WO PCT/DE2003/002319 patent/WO2004014815A1/de not_active Application Discontinuation
- 2003-07-10 AU AU2003254624A patent/AU2003254624A1/en not_active Abandoned
- 2003-07-10 DE DE10393341T patent/DE10393341D2/de not_active Expired - Fee Related
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1604405A (en) * | 1978-05-31 | 1981-12-09 | Univ Cardiff | Articles made from resin compositions containing aggregate materials eg glass |
WO1989011457A1 (en) * | 1988-05-27 | 1989-11-30 | Schultze Kraft Andreas | Process for producing artificial stones, and their use |
DE4334623A1 (de) * | 1993-10-06 | 1995-04-13 | Grundstuecks Verwaltung Frenze | Behandlung von Glasbruch als Zuschlagstoff in Mineralstoffgemischen |
DE4402432A1 (de) * | 1994-01-27 | 1995-08-03 | Schultze Kraft Andreas | Oberflächenbeschichtete Granulate und Formteile für die Herstellung von Formteilen aus Polymerkunststein und Polymerbeton |
WO2001007528A1 (en) * | 1999-07-22 | 2001-02-01 | Ppg Industries Ohio, Inc. | Pigmented coatings for ceramic substrates |
WO2002076904A2 (de) * | 2001-03-27 | 2002-10-03 | Pur-Bauchemie Gmbh | Glashaltiger baustoffkörper oder -belag |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9464003B2 (en) | 2009-06-24 | 2016-10-11 | Basf Se | Method of producing a composite material using a mixing system |
US9896381B2 (en) | 2009-06-24 | 2018-02-20 | Basf Se | Method of producing a composite material using a mixing system |
US10040721B2 (en) | 2009-06-24 | 2018-08-07 | Basf Se | Method of producing a composite material using a mixing system |
DE202009013082U1 (de) | 2009-10-01 | 2010-02-25 | Schultze-Kraft, Andreas | Trivalent beschichtetes Glasgranulat als Betonzuschlag |
WO2011038722A2 (de) | 2009-10-01 | 2011-04-07 | Andreas Schultze-Kraft | Trivalent beschichtetes glasgranulat als betonzuschlag |
WO2011038722A3 (de) * | 2009-10-01 | 2011-05-26 | Andreas Schultze-Kraft | Beschichtetes glasgranulat als betonzuschlag |
US9505931B2 (en) | 2009-12-21 | 2016-11-29 | Basf Se | Composite pavement structure |
US10253460B2 (en) | 2009-12-21 | 2019-04-09 | Basf Se | Composite pavement structure |
JP2014501344A (ja) * | 2010-12-29 | 2014-01-20 | ビーエーエスエフ ソシエタス・ヨーロピア | 着色複合舗装構造 |
US9856363B2 (en) | 2010-12-29 | 2018-01-02 | Basf Se | Colored composite pavement structure |
RU2565671C1 (ru) * | 2014-05-30 | 2015-10-20 | Федеральное государственное бюджетное учреждение науки Институт синтетических полимерных материалов им. Н.С. Ениколопова Российской академии наук (ИСПМ РАН) | Разветвленные фторсодержащие кремнийорганические сополимеры, способ их получения и гидрофобное полимерное покрытие на их основе |
Also Published As
Publication number | Publication date |
---|---|
AU2003254624A1 (en) | 2004-02-25 |
EP1523457A1 (de) | 2005-04-20 |
DE10393341D2 (de) | 2005-06-16 |
DE10231858A1 (de) | 2004-01-22 |
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