WO2001040133A2 - Organic pigment dispersion for coloring building materials - Google Patents

Organic pigment dispersion for coloring building materials Download PDF

Info

Publication number
WO2001040133A2
WO2001040133A2 PCT/US2000/042510 US0042510W WO0140133A2 WO 2001040133 A2 WO2001040133 A2 WO 2001040133A2 US 0042510 W US0042510 W US 0042510W WO 0140133 A2 WO0140133 A2 WO 0140133A2
Authority
WO
WIPO (PCT)
Prior art keywords
dispersion
organic
organic pigment
dispersing agent
pigment
Prior art date
Application number
PCT/US2000/042510
Other languages
French (fr)
Other versions
WO2001040133A3 (en
Inventor
Charles W. Perry
Donald C. Dulaney
James E. Moore
Original Assignee
Sun Chemical Corporation
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sun Chemical Corporation filed Critical Sun Chemical Corporation
Priority to CA2393425A priority Critical patent/CA2393425C/en
Priority to US10/148,037 priority patent/US6786965B2/en
Priority to DE60027460T priority patent/DE60027460T2/en
Priority to EP00992176A priority patent/EP1237825B1/en
Publication of WO2001040133A2 publication Critical patent/WO2001040133A2/en
Publication of WO2001040133A3 publication Critical patent/WO2001040133A3/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B40/00Processes, in general, for influencing or modifying the properties of mortars, concrete or artificial stone compositions, e.g. their setting or hardening ability
    • C04B40/0028Aspects relating to the mixing step of the mortar preparation
    • C04B40/0039Premixtures of ingredients
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B16/00Use of organic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of organic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone

Definitions

  • This invention relates to an aqueous dispersion of organic pigment suitable for coloring building materials such as concrete, asphalt, plaster, mortar and cement mortar. More particularly, this invention relates to aqueous dispersions which contain silica binder, an organic pigment and dispersing agent.
  • Colored concrete buildings do not present an environment as sterile and cold as white concrete.
  • light colors can be used in sunny climates to help reduce glare while darker colors may be used to increase a building's heat storage capacity in cooler climates.
  • any color additive must be uniformly dispersed throughout the building material. This can be difficult given the low intensity mixing and short mixing times customary in the building materials industry. Moreover, the additive must not adversely affect the desirable properties of the building material such as the strength or setting behavior of concrete or reduce the compressive strength or abrasion resistance of asphalt. See ASTM C 979-82 "Standard Specification for Pigments for Integrally Colored Concrete, " which contains some of the industry association standards for coloring concrete.
  • Inorganic pigments are typically used as color additives for building materials and typically include iron oxides (natural and synthetic) , chromium oxide, cobalt blue, titanium dioxide and carbon black. However, these inorganic pigments offer a limited ranges of colors and brightness.
  • Organic pigments have not been used to color building materials as it is believed they lack sufficient alkali resistance and lightfastness .
  • ASTM American Society for Testing and Materials
  • dry pigment powders have been used to color concrete compositions because they are highly dispersible. However, these powders have poor processing properties, and typically cake together and form lumps upon storage. They also tend to form dust .
  • U.S. Patent No. 5,401,313 discloses a pigment particle whose surface is coated with an electric charge modifying agent and a dispersion promoting agent.
  • the dispersion promoting agent is selected from stearates, acetates, alkylphenols, cellulosics, waxes, lignins, acrylics, epoxies, urethanes, ethylenes, styrenes, propylenes and polymers having functions groups of alcohols, glycols, aldehydes, amides and carboxylic acids, and is preferably sodium lignosulfonate for cementitious application systems.
  • the surface-modified particle may be produced in powder, dispersion or granular form, with bead granules having a particle size of 25 to 250 microns being preferred.
  • An object of the invention is to provide aqueous organic pigment dispersions for coloring concrete and which exhibit acceptable alkali resistance and lightfastness.
  • the inventive dispersion is a combination of organic pigment, silica and water.
  • An advantage of the present invention is the ability to color building materials such as concrete with bright organic pigments that do not suffer from poor alkali resistance and/or poor lightfastness.
  • Another advantage of the present invention is that it permits the ready removal of graffiti or other surface defacement from a concrete surface without impairing its surface appearance.
  • the present invention relates to an aqueous based organic pigment dispersion, comprising (i) silica binder;
  • the present invention relates to a method for preparing organic pigment dispersions which includes
  • Any silica may be used in the organic dispersion of the present invention if it is effective to cause the pigment to adhere to the building material.
  • Suitable silicas include silicate, metasilicate pentahydrate, sesquisilicate and orthosilicate. Alkali metal silicates are preferred, with sodium and potassium silicates being especially preferred. Such silicates are commercially available as aqueous dispersions.
  • Any organic pigment can be used in the organic dispersion of the present invention if it exhibits good alkali resistance and light resistance, as determined according to ASTM C 979-82, herein incorporated in its entirety by reference. Thus, those organic pigments which cannot withstand a pH of 10 or greater will not be useful in the aqueous pigment dispersion of the present invention.
  • Suitable organic pigments may be chosen from azo pigments, such as azo lake, azo chelate and condensed azo pigments, and polycyclic pigments such as phthalocyanine pigments, perylene pigments, perinone pigments, anthraquinone pigments, quinacridone pigments, dioxazine pigments, thioindigo pigments, isoindolinone pigments and quinophethalone pigments.
  • Preferred organic pigments are selected from phthalocyanine green, phthalocyanine blue, carbazole violet, toluidine red, perylene red, qumacridone red, qumacridone yellow, Dalamar yellow and Watchung red.
  • Any dispersing agent can be used in the organic dispersion of the present invention provided that it effectively disperses the binder and organic pigment in water.
  • a given dispersing agent's effectiveness can be optimized by varying the amount of dissolved silica present and by adjusting the dispersion's pH to between 10 and 14, preferably between 11 and 12.
  • Suitable dispersing agents include alkylbenzene sulfomc acid salts, alkylnaphthalene sulfomc acid salts, naphthalene sulfomc acid salts, melamine-formaldehyde condensates, polysaccha ⁇ de resins, sytrenated acrylic resins, octylphenol polyethoxylated surfactants, non-ionic acetylenic diol surfactants, ethoxylated oleyl alcohol surfactants and phosphate ester surfactants.
  • a sodium salt of naphthalenesufonic acid commercially available from Rohm & Haas Co. under the trademark TAMOL SN, is preferred along with diethylene glycol monomethyl ether acetate.
  • the organic pigment dispersions of the present invention typically contain at least 10% by weight silica, at least 30% by weight of organic pigment, at least 1% by weight dispersing agent, with the remainder water.
  • the dispersing agent is typically present in an amount of from 1-10%, preferably 1-5%, by weight.
  • Silica is preferably present in an amount of at least 30% by weight.
  • Other compounds may be present in any amount which does not detract from the organic dispersion's effectiveness in integrally coloring building materials such as concrete.
  • Hydroxyalkyl celluloses such as hydroxyethylcellulose, are preferably added to the aqueous dispersion to increase its viscosity to a range of from 800 to 10,000 centipoise, preferably 1,000 to 2,000 centipoise, at 25 * C.
  • the amount of viscosity additive will depend on the relative amounts of dispersing agent, binder, organic pigment and water forming the dispersion, and may range from 0.1% to 2% by weight of the dispersion.
  • the organic pigment dispersions of the present invention may be prepared by a three-stage process.
  • the silica binder, organic pigment and dispersing agent are mixed together in the desired amounts to form a dispersion premix which contains the dispersing agent and organic pigment uniformly distributed throughout the silica binder.
  • Conventional high speed mixing equipment may be used without modification under the trade name Dispersmat.
  • a mixing speed of from 3,000 to 10,000 rpm for a time period of from 1 minute to 2 hours, preferably 10- 25 minutes, may be used depending on the size of the batch.
  • the dispersion premix is media milled, typically using glass milling beads, to reduce the size of the organic pigment particles to an average particle size range of from about 100 to about 300 nanometers, thereby forming a non- standardized dispersion.
  • Media milling can be performed using conventional milling equipment without modification.
  • water is added to the non- standardized dispersion until the color of the dispersion matches a color standard. Generally from 5 to 10%, by weight, water is required to standardize the dispersion.
  • the inventors currently believe that the alkali metal silica particles chemically reacts with the building material, thereby "locking" the pigment into the building material and preventing washout of the color, with no reduction in strength of the building material. This chemical reaction prevents streaking and staining of the integrally colored concrete over time, and eliminates any need for an overcoat.
  • the organic dispersion of the present invention may be used to integrally color building materials such as cement, asphalts, plaster, mortar and cement mortar at the construction site. More particularly, the organic dispersion may be added to the building material as it is being formulated. Thus, for example, from 0.5% to 10% by weight, preferably 2-3% by weight, of the organic dispersion may be added to a concrete mixer containing Portland cement, sand/gravel aggregate and water, and homogenized for approximately 15 - 30 minutes. The resulting mixture may be poured into a prepared mold and allowed to harden to form integrally colored concrete.
  • Example 1 Formulation of an Organic Dispersion
  • a high speed mixer was used to mix potassium silicate, hydroxyethylcellulose, phthalocyanine green (C.I. Pigment Green 7), the sodium salt of naphthalenesulfonic acid (TAMOL SN, commercially available from Rohm & Haas Co.) and water to form a dispersion precursor, which was then media milled (Eiger mixer) to disperse and incorporate the pigment into the binder system.
  • the resulting organic dispersion had a resin solids (potassium silicate binder) percentage of 13.60% and a total solids percentage of 56.60%.
  • the weight percentage composition of the organic dispersion is set forth below in Table 1:
  • the organic dispersions of Examples 1 and 2 were each individually used to integrally color concrete by mixing an appropriate amount (1 %) of the dispersion with concrete in a laboratory mixer for approximately 15 minutes. Each of the organic dispersions readily became part of the concrete matrix.

Abstract

An aqueous organic pigment dispersion used to integrally color concrete and other building materials which includes: alkali metal silica particles as a binder, organic pigment, water and dispersing agent. A method for preparing the aqueous organic pigment dispersion includes (i) mixing alkali metal silica particles, organi c pigment, and dispersing agent; (ii) milling the dispersion precursor in a mixer filled with glass beads for a period of time sufficient to reduce the particle size of the organic pigment to about 100 to about 300 nanometers, thereby forming a non-standardized dispersion; and (iii) standardizing the dispersion against a color standard by adding water.

Description

TITLE: ORGANIC PIGMENT DISPERSION FOR COLORING BUILDING MATERIALS
BACKGROUND OF THE INVENTION:
1. Field of the Invention
This invention relates to an aqueous dispersion of organic pigment suitable for coloring building materials such as concrete, asphalt, plaster, mortar and cement mortar. More particularly, this invention relates to aqueous dispersions which contain silica binder, an organic pigment and dispersing agent.
2. Description of the prior art
It is desirable to color exposed concrete surfaces for both aesthetic and functional reasons. Colored concrete buildings do not present an environment as sterile and cold as white concrete. In addition, light colors can be used in sunny climates to help reduce glare while darker colors may be used to increase a building's heat storage capacity in cooler climates.
Coloring the exposed surface by painting or by coating the surface with some other decorative layer is known. U.S. Patent Nos. 2,549,516; 3,929,692 and 4,134,956 disclose compositions for covering exposed concrete surfaces. However, painting or application of a coating layer is an additional step in construction which adds cost and complexity to a construction project. Moreover, an exterior painted surface may require repainting in a relatively short period of time.
Another approach is to add a color additive to the building material, thereby eliminating the extra step associated with painting the building surface. However, any color additive must be uniformly dispersed throughout the building material. This can be difficult given the low intensity mixing and short mixing times customary in the building materials industry. Moreover, the additive must not adversely affect the desirable properties of the building material such as the strength or setting behavior of concrete or reduce the compressive strength or abrasion resistance of asphalt. See ASTM C 979-82 "Standard Specification for Pigments for Integrally Colored Concrete, " which contains some of the industry association standards for coloring concrete.
Inorganic pigments are typically used as color additives for building materials and typically include iron oxides (natural and synthetic) , chromium oxide, cobalt blue, titanium dioxide and carbon black. However, these inorganic pigments offer a limited ranges of colors and brightness.
Organic pigments have not been used to color building materials as it is believed they lack sufficient alkali resistance and lightfastness . In 1981 the American Society for Testing and Materials (ASTM) in a report entitled "Pigments for Integrally Colored Concrete, " discussed the test results of various inorganic and organic pigments for lightfastness, alkali resistance, water wettability and curing stability. All of the organic pigments tested, including phthalocyanine green, failed to meet the lightfastness testing standards. Dry pigment powders have been used to color concrete compositions because they are highly dispersible. However, these powders have poor processing properties, and typically cake together and form lumps upon storage. They also tend to form dust .
The use of free flowing granules or beads to overcome the processing problems and dust associated with dry pigment powders has been suggested. These granules may be produced by spray drying aqueous dispersions, as proposed by U.S. Patent Nos . 4,946,505; 5,484,481; 5,853,476; and 5,882,395. However, the evaporation of the aqueous dispersion requires expensive equipment and significant energy expenditures which can make the use of such granules economically unattractive.
Another approach is to modify the particle's surface to improve its dispersibility in aqueous solution. U.S. Patent No. 5,401,313 discloses a pigment particle whose surface is coated with an electric charge modifying agent and a dispersion promoting agent. The dispersion promoting agent is selected from stearates, acetates, alkylphenols, cellulosics, waxes, lignins, acrylics, epoxies, urethanes, ethylenes, styrenes, propylenes and polymers having functions groups of alcohols, glycols, aldehydes, amides and carboxylic acids, and is preferably sodium lignosulfonate for cementitious application systems. The surface-modified particle may be produced in powder, dispersion or granular form, with bead granules having a particle size of 25 to 250 microns being preferred. An object of the invention is to provide aqueous organic pigment dispersions for coloring concrete and which exhibit acceptable alkali resistance and lightfastness.
The inventive dispersion is a combination of organic pigment, silica and water.
An advantage of the present invention is the ability to color building materials such as concrete with bright organic pigments that do not suffer from poor alkali resistance and/or poor lightfastness.
Another advantage of the present invention is that it permits the ready removal of graffiti or other surface defacement from a concrete surface without impairing its surface appearance.
SUMMARY OF THE INVENTION:
In one aspect, the present invention relates to an aqueous based organic pigment dispersion, comprising (i) silica binder;
(ii) organic pigment;
(iii) dispersing agent; and
(iv) water.
In another aspect, the present invention relates to a method for preparing organic pigment dispersions which includes
(i) mixing, at 3,000 to 10,000 rpm, a silica binder, organic pigment and dispersing agent, to form a dispersion premix;
(ii) milling the dispersion premix in a mixer filled with glass beads for a period of time sufficient to reduce the particle size of the organic pigment to from about 100 to about 300 nanometers, thereby forming a non-standardized dispersion; (iii) adding water to the non-standardized dispersion until it matches a color standard and forms an organic dispersion.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS:
Any silica may be used in the organic dispersion of the present invention if it is effective to cause the pigment to adhere to the building material. Suitable silicas include silicate, metasilicate pentahydrate, sesquisilicate and orthosilicate. Alkali metal silicates are preferred, with sodium and potassium silicates being especially preferred. Such silicates are commercially available as aqueous dispersions.
Any organic pigment can be used in the organic dispersion of the present invention if it exhibits good alkali resistance and light resistance, as determined according to ASTM C 979-82, herein incorporated in its entirety by reference. Thus, those organic pigments which cannot withstand a pH of 10 or greater will not be useful in the aqueous pigment dispersion of the present invention. Suitable organic pigments may be chosen from azo pigments, such as azo lake, azo chelate and condensed azo pigments, and polycyclic pigments such as phthalocyanine pigments, perylene pigments, perinone pigments, anthraquinone pigments, quinacridone pigments, dioxazine pigments, thioindigo pigments, isoindolinone pigments and quinophethalone pigments. Preferred organic pigments are selected from phthalocyanine green, phthalocyanine blue, carbazole violet, toluidine red, perylene red, qumacridone red, qumacridone yellow, Dalamar yellow and Watchung red.
Any dispersing agent can be used in the organic dispersion of the present invention provided that it effectively disperses the binder and organic pigment in water. A given dispersing agent's effectiveness can be optimized by varying the amount of dissolved silica present and by adjusting the dispersion's pH to between 10 and 14, preferably between 11 and 12. Suitable dispersing agents include alkylbenzene sulfomc acid salts, alkylnaphthalene sulfomc acid salts, naphthalene sulfomc acid salts, melamine-formaldehyde condensates, polysacchaπde resins, sytrenated acrylic resins, octylphenol polyethoxylated surfactants, non-ionic acetylenic diol surfactants, ethoxylated oleyl alcohol surfactants and phosphate ester surfactants. A sodium salt of naphthalenesufonic acid, commercially available from Rohm & Haas Co. under the trademark TAMOL SN, is preferred along with diethylene glycol monomethyl ether acetate.
The organic pigment dispersions of the present invention typically contain at least 10% by weight silica, at least 30% by weight of organic pigment, at least 1% by weight dispersing agent, with the remainder water. The dispersing agent is typically present in an amount of from 1-10%, preferably 1-5%, by weight. Silica is preferably present in an amount of at least 30% by weight. Other compounds may be present in any amount which does not detract from the organic dispersion's effectiveness in integrally coloring building materials such as concrete. Hydroxyalkyl celluloses, such as hydroxyethylcellulose, are preferably added to the aqueous dispersion to increase its viscosity to a range of from 800 to 10,000 centipoise, preferably 1,000 to 2,000 centipoise, at 25 *C. The amount of viscosity additive will depend on the relative amounts of dispersing agent, binder, organic pigment and water forming the dispersion, and may range from 0.1% to 2% by weight of the dispersion.
The organic pigment dispersions of the present invention may be prepared by a three-stage process. In the first stage, the silica binder, organic pigment and dispersing agent are mixed together in the desired amounts to form a dispersion premix which contains the dispersing agent and organic pigment uniformly distributed throughout the silica binder. Conventional high speed mixing equipment may be used without modification under the trade name Dispersmat. A mixing speed of from 3,000 to 10,000 rpm for a time period of from 1 minute to 2 hours, preferably 10- 25 minutes, may be used depending on the size of the batch.
In the second stage, the dispersion premix is media milled, typically using glass milling beads, to reduce the size of the organic pigment particles to an average particle size range of from about 100 to about 300 nanometers, thereby forming a non- standardized dispersion. Media milling can be performed using conventional milling equipment without modification. In the third and final stage, water is added to the non- standardized dispersion until the color of the dispersion matches a color standard. Generally from 5 to 10%, by weight, water is required to standardize the dispersion.
Without intending to be bound by theory, the inventors currently believe that the alkali metal silica particles chemically reacts with the building material, thereby "locking" the pigment into the building material and preventing washout of the color, with no reduction in strength of the building material. This chemical reaction prevents streaking and staining of the integrally colored concrete over time, and eliminates any need for an overcoat.
The organic dispersion of the present invention may be used to integrally color building materials such as cement, asphalts, plaster, mortar and cement mortar at the construction site. More particularly, the organic dispersion may be added to the building material as it is being formulated. Thus, for example, from 0.5% to 10% by weight, preferably 2-3% by weight, of the organic dispersion may be added to a concrete mixer containing Portland cement, sand/gravel aggregate and water, and homogenized for approximately 15 - 30 minutes. The resulting mixture may be poured into a prepared mold and allowed to harden to form integrally colored concrete.
The following examples illustrate preferred embodiments of the invention, and are not intended to limit the scope of the invention in any manner whatsoever. Example 1 Formulation of an Organic Dispersion A high speed mixer was used to mix potassium silicate, hydroxyethylcellulose, phthalocyanine green (C.I. Pigment Green 7), the sodium salt of naphthalenesulfonic acid (TAMOL SN, commercially available from Rohm & Haas Co.) and water to form a dispersion precursor, which was then media milled (Eiger mixer) to disperse and incorporate the pigment into the binder system. The resulting organic dispersion had a resin solids (potassium silicate binder) percentage of 13.60% and a total solids percentage of 56.60%. The weight percentage composition of the organic dispersion is set forth below in Table 1:
TABLE 1
Figure imgf000010_0001
Example 2
Formulation of an Organic Dispersion
Several other organic dispersions were formulated using the general procedures of Example 1. The composition weight percentages of the various materials of these organic dispersions are set forth below in Table 2. TABLE 2
Figure imgf000011_0001
Example 3 Integrally Coloring Concrete
The organic dispersions of Examples 1 and 2 were each individually used to integrally color concrete by mixing an appropriate amount (1 %) of the dispersion with concrete in a laboratory mixer for approximately 15 minutes. Each of the organic dispersions readily became part of the concrete matrix.

Claims

CLAIMS :
1. An organic pigment dispersion comprising:
(i) silica binder; (ii) organic pigment; (iii) dispersing agent; and (iv) water.
2. The organic dispersion of claim 1, wherein the silica binder is selected from the group consisting of silicate, metasilicate pentahydrate, sesquisilicate and orthosilicate.
3. The organic dispersion of claim 2, wherein the silica is a sodium silicate.
4. The organic dispersion of claim 1, wherein said organic pigment is selected from the group consisting of phthalocyanine green, phthalocyanine blue, carbazole violet, toluidine red, Dalamar yellow and Watchung red.
5. The organic dispersion of claim 1, wherein said organic pigment is a phthalocyanine.
6. The organic dispersion of claim 1, wherein said dispersing agent is selected from the group consisting of an alkylbenzene sulfonic acid salt, an alkylnaphthalene sulfonic acid salt, a naphthalene sulfonic acid salt, a melamine-formaldehyde condensates, a polysaccharide resin, a styrenated acrylic resin, an octylphenol polyethoxylated surfactant, a non-ionic acetylenic diol surfactant, an ethoxylated oleyl alcohol surfactant and phosphate ester surfactant.
7. The organic dispersion of claim 6, wherein said dispersing agent is a sodium salt of naphthalene sulfonic acid.
8. The organic dispersion of claim 5, wherein said dispersing agent is diethylene glycol monomethyl ether acetate.
9. The organic dispersion of claim 1, further comprising a hydroxyalkylcellulose.
10. The organic dispersion of claim 9, wherein said hydroxyalkylcellulose is a hydroxyethylcellulose.
11. The organic dispersion of claim 1, wherein said organic pigment has an average particle size of from 100 to 300 nanometers .
12. A process for preparing an organic pigment dispersion, comprising: (i) mixing at 3,000 to 10,000 rpm, a silica binder, organic pigment and dispersing agent to form a dispersion premix;
(ii) milling the dispersion premix in a mixer filled with glass beads for a period of time sufficient to reduce the particle size of the organic pigment to about 100 to about 300 nanometers, thereby forming a non-standardized dispersion; and
(iii) adding water to the non-standardized dispersion until it matches a color standard and forms an organic dispersion .
13. A colored building material, comprising the organic pigment dispersion of claim 1 dispersed in a building material.
PCT/US2000/042510 1999-12-03 2000-12-04 Organic pigment dispersion for coloring building materials WO2001040133A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CA2393425A CA2393425C (en) 1999-12-03 2000-12-04 Organic pigment dispersion for coloring building materials
US10/148,037 US6786965B2 (en) 1999-12-03 2000-12-04 Organic pigment dispersion for coloring building materials
DE60027460T DE60027460T2 (en) 1999-12-03 2000-12-04 ORGANIC PIGMENT DISPERSION FOR STAINING BUILDING MATERIALS
EP00992176A EP1237825B1 (en) 1999-12-03 2000-12-04 Organic pigment dispersion for coloring building materials

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16889799P 1999-12-03 1999-12-03
US60/168,897 1999-12-03

Publications (2)

Publication Number Publication Date
WO2001040133A2 true WO2001040133A2 (en) 2001-06-07
WO2001040133A3 WO2001040133A3 (en) 2001-12-13

Family

ID=22613406

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2000/042510 WO2001040133A2 (en) 1999-12-03 2000-12-04 Organic pigment dispersion for coloring building materials

Country Status (6)

Country Link
US (1) US6786965B2 (en)
EP (1) EP1237825B1 (en)
CA (1) CA2393425C (en)
DE (1) DE60027460T2 (en)
DK (1) DK1237825T3 (en)
WO (1) WO2001040133A2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004085548A3 (en) * 2003-03-27 2004-11-18 Constr Res & Tech Gmbh Liquid coloring suspension
FR2865730A1 (en) * 2004-02-03 2005-08-05 Norbert Vial Colorant for coatings and mortars in the form of an aqueous dispersion that can be readily mixed on site for building industry applications
CH713400A1 (en) * 2017-01-31 2018-07-31 Peter Buetzer Process for the preparation of hydraulically setting building materials with hydrophobic blue and / or black pigments by means of liquefiers or flow agents.

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6902613B2 (en) * 2002-11-27 2005-06-07 Ciba Specialty Chemicals Corporation Preparation and use of nanosize pigment compositions
GB0308487D0 (en) * 2003-04-14 2003-05-21 Ciba Spec Chem Water Treat Ltd Paper coating compositions
CA2530734A1 (en) * 2003-06-24 2005-01-06 Semyon A. Shimanovich Pigment paste for concrete and method for making the same
AU2004253945B2 (en) * 2003-06-26 2009-02-19 Playtex Products, Inc. A coating composition and articles coated therewith
US7241500B2 (en) 2003-10-06 2007-07-10 Certainteed Corporation Colored roofing granules with increased solar heat reflectance, solar heat-reflective shingles, and process for producing same
EP2447327B1 (en) * 2003-11-28 2013-07-31 Daicel Chemical Industries, Ltd. Dispersion and process for producing colored organic solid particle
EP1557448B1 (en) * 2004-01-26 2011-06-08 Dainichiseika Color & Chemicals Mfg. Co., Ltd. Wet grinding process using microbeads
US20070107632A1 (en) * 2005-10-28 2007-05-17 Ball Richard L Pigmented wall and ceiling spackle
US7815728B2 (en) * 2008-05-02 2010-10-19 L. M. Scofield Company High SRI cementitious systems for colored concrete
DE102010003999A1 (en) * 2009-05-12 2011-01-05 Harold Scholz & Co. Gmbh New pigment systems for coloring cementitious systems, in particular concrete
KR100938557B1 (en) * 2009-06-10 2010-01-22 (주)나노스톤 Coloring method for nature stone
WO2011022011A1 (en) 2009-08-20 2011-02-24 Certainteed Corporation Roofing granules, roofing products including such granules, and process for preparing same
US8637116B2 (en) 2009-08-20 2014-01-28 Certainteed Corporation Process for preparing roofing granules comprising organic colorant, with improved luster, and roofing products including such granules
US9850166B2 (en) 2015-02-03 2017-12-26 Construction Research & Technology, Gmbh Liquid coloring suspension and colored cementitious composition
RU2716130C9 (en) * 2016-10-03 2020-05-21 Дзе Проктер Энд Гэмбл Компани Detergent composition for washing
MX2019003839A (en) * 2016-10-03 2019-06-24 Procter & Gamble Laundry detergent composition.
MX2019003884A (en) * 2016-10-03 2019-06-10 Procter & Gamble Low ph laundry detergent composition.

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB217633A (en) * 1923-03-13 1924-06-13 Master Builders Co Process and composition of matter for colouring mortars and concretes
US1900216A (en) * 1929-01-28 1933-03-07 Witt Joshua Chitwood Coloring material
US4134956A (en) * 1972-11-14 1979-01-16 Kowa Chemical Industry Ltd. Method of forming a decorative layer on a precast concrete board
EP0467165A1 (en) * 1990-07-06 1992-01-22 Walhalla-Kalk Entwicklungs- und Vertriebsgesellschaft mbH Solids suspensions stable against sedimentation and process for their preparation
EP0482450A1 (en) * 1990-10-24 1992-04-29 Bayer Ag Process for colouring building materials
US5558708A (en) * 1995-05-11 1996-09-24 C-Cure Corporation System and method for dispersing pigment in cement based compositions
EP0742186A1 (en) * 1995-05-11 1996-11-13 C-Cure Corporation A composition and method for dispersing pigment in cement based compositions
DE19533081A1 (en) * 1995-09-07 1997-03-13 Braas Gmbh Process for the production of colored concrete bodies
US5853476A (en) * 1997-08-11 1998-12-29 Elementis Pigments, Inc. Process for coloring concrete using compacted inorganic granules

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549516A (en) 1946-04-06 1951-04-17 Johns Manville Structural unit and method of manufacture
US3929692A (en) 1973-03-06 1975-12-30 Grow Chemical Corp Sprayable decorative coating composition for covering unfinished surfaces
DE2604569A1 (en) * 1976-02-06 1977-08-18 Baerle & Co Kg Van Stable aq. dispersions of pigments - mixed with aq. alkali silicates to form paints
JPS5367729A (en) * 1976-11-30 1978-06-16 Dainichi Seika Kogyo Kk Aqueous pigment dispersion
JPS5667371A (en) * 1979-11-06 1981-06-06 Mitsubishi Paper Mills Ltd Preparation of composition for coated paper
JPS6081012A (en) * 1983-10-06 1985-05-09 Miyoshi Kasei:Kk Fine globular colored silica gel and its manufacture
DE3619363A1 (en) 1986-06-09 1987-12-10 Brockhues Chem Werke Ag METHOD FOR COLORING CONCRETE
US5401313A (en) 1993-02-10 1995-03-28 Harcros Pigments, Inc. Surface modified particles and method of making the same
DE4336613C1 (en) 1993-10-27 1995-02-09 Bayer Ag Process for colouring building materials
JPH09100148A (en) * 1995-10-05 1997-04-15 Toyo Ink Mfg Co Ltd Colored cement-cured composition
DE19632928A1 (en) 1996-08-16 1998-02-19 Bayer Ag Process for the preparation of inorganic granules and their use
US5897698A (en) * 1996-10-18 1999-04-27 Huls America Inc. Non-settling , universal machine dispensable pearlescent pigment dispersions
AR011260A1 (en) * 1996-10-18 2000-08-16 Huls America Inc A DIVERSION COMPOSITION OF UNIVERSAL PEARL PIGMENT SUPPLIED THROUGH DISPERSING MACHINES, TO BE USED IN A SURFACE COATING AND A METHOD FOR PREPARING IT
DE19811791A1 (en) * 1998-03-18 1999-09-23 Borchers Gmbh Aqueous dispersions with a special combination of dispersants
JP2002373608A (en) * 2001-06-14 2002-12-26 Hitachi Chem Co Ltd Solution for forming surface treated film

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB217633A (en) * 1923-03-13 1924-06-13 Master Builders Co Process and composition of matter for colouring mortars and concretes
US1900216A (en) * 1929-01-28 1933-03-07 Witt Joshua Chitwood Coloring material
US4134956A (en) * 1972-11-14 1979-01-16 Kowa Chemical Industry Ltd. Method of forming a decorative layer on a precast concrete board
EP0467165A1 (en) * 1990-07-06 1992-01-22 Walhalla-Kalk Entwicklungs- und Vertriebsgesellschaft mbH Solids suspensions stable against sedimentation and process for their preparation
EP0482450A1 (en) * 1990-10-24 1992-04-29 Bayer Ag Process for colouring building materials
US5558708A (en) * 1995-05-11 1996-09-24 C-Cure Corporation System and method for dispersing pigment in cement based compositions
EP0742186A1 (en) * 1995-05-11 1996-11-13 C-Cure Corporation A composition and method for dispersing pigment in cement based compositions
DE19533081A1 (en) * 1995-09-07 1997-03-13 Braas Gmbh Process for the production of colored concrete bodies
US5853476A (en) * 1997-08-11 1998-12-29 Elementis Pigments, Inc. Process for coloring concrete using compacted inorganic granules

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 197015 Derwent Publications Ltd., London, GB; AN 1970-24242r XP002176468 & SU 247 831 A (KRAMATOR TILE FACTORY) *
DATABASE WPI Week 197830 Derwent Publications Ltd., London, GB; AN 1978-54043a XP002176466 & JP 53 067729 A (DAINI SEIKOSHA KK) *
DATABASE WPI Week 198319 Derwent Publications Ltd., London, GB; AN 1983-45343K XP002176467 & JP 05 855356 A (NIPPON KOKAN KK) *
PATENT ABSTRACTS OF JAPAN vol. 1997, no. 08, 29 August 1997 (1997-08-29) & JP 09 100148 A (TOYO INK MFG) *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004085548A3 (en) * 2003-03-27 2004-11-18 Constr Res & Tech Gmbh Liquid coloring suspension
US7497904B2 (en) 2003-03-27 2009-03-03 Construction Research & Technology Gmbh Liquid coloring suspension and colored cementitious composition
FR2865730A1 (en) * 2004-02-03 2005-08-05 Norbert Vial Colorant for coatings and mortars in the form of an aqueous dispersion that can be readily mixed on site for building industry applications
CH713400A1 (en) * 2017-01-31 2018-07-31 Peter Buetzer Process for the preparation of hydraulically setting building materials with hydrophobic blue and / or black pigments by means of liquefiers or flow agents.

Also Published As

Publication number Publication date
DE60027460D1 (en) 2006-05-24
US20030047118A1 (en) 2003-03-13
EP1237825A2 (en) 2002-09-11
EP1237825B1 (en) 2006-04-19
DK1237825T3 (en) 2006-08-21
CA2393425C (en) 2011-02-08
US6786965B2 (en) 2004-09-07
WO2001040133A3 (en) 2001-12-13
DE60027460T2 (en) 2006-10-12
CA2393425A1 (en) 2001-06-07

Similar Documents

Publication Publication Date Title
CA2393425C (en) Organic pigment dispersion for coloring building materials
US7999017B2 (en) Method for coloring building materials using a cationic pigment dispersion
AU2004234531B2 (en) Quickly disintegrating pigment concentrate
CN108456475A (en) A kind of high adhesion force Waterproof priming paint and its preparation method and application
JPH09124970A (en) Composition and method for dispersing pigment in cement-basecompound
CN101421361B (en) Black pigment/auxiliary combination having improved color strength
US6090329A (en) Method of producing colored concrete bodies such as colored concrete roofing tiles
US3117882A (en) Process for coloring inorganic cementitious materials
CN113604123B (en) Water-in-water coating capable of adjusting color externally and application thereof
US6515062B2 (en) Decorative synthetic stucco compositions
WO2008112946A1 (en) Water-based polyurethane pigmented coating
US6201050B1 (en) Breakable gel additive carrier for ionic compositions
US9382158B2 (en) Method of preparing a coloured self-levelling cementitious floor covering
JP6585203B2 (en) Cool feeling paint composition
US6696162B2 (en) Paint and coating compositions containing tantalum and/or niobium powders
JPH07247443A (en) Wet powdery pigment composition and its production
CN1854102A (en) Method of using pigment in concrete products
EP1401783B1 (en) Breakable gel additive carrier for ionic compositions
CN116000236A (en) Coating for powder casting and preparation and use methods thereof
KR20210082490A (en) Masonry Composition Comprising Chemically Treated Carbon Pigment
JP2002273716A (en) Method for manufacturing colored inorganic board
WO2001051553A1 (en) Colored building materials
JPH04362048A (en) Water-permeable cement pavement composition

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): CA US

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
AK Designated states

Kind code of ref document: A3

Designated state(s): CA US

AL Designated countries for regional patents

Kind code of ref document: A3

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE TR

WWE Wipo information: entry into national phase

Ref document number: 2393425

Country of ref document: CA

WWE Wipo information: entry into national phase

Ref document number: 2000992176

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 10148037

Country of ref document: US

WWP Wipo information: published in national office

Ref document number: 2000992176

Country of ref document: EP

WWG Wipo information: grant in national office

Ref document number: 2000992176

Country of ref document: EP