GB2065157A - Method of Producing Cement Colouring Composition - Google Patents
Method of Producing Cement Colouring Composition Download PDFInfo
- Publication number
- GB2065157A GB2065157A GB7943385A GB7943385A GB2065157A GB 2065157 A GB2065157 A GB 2065157A GB 7943385 A GB7943385 A GB 7943385A GB 7943385 A GB7943385 A GB 7943385A GB 2065157 A GB2065157 A GB 2065157A
- Authority
- GB
- United Kingdom
- Prior art keywords
- slurry
- pigment
- dispersant
- aqueous carrier
- stabilizer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- 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
- C04B28/02—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 hydraulic cements other than calcium sulfates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09C—TREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
- C09C3/00—Treatment in general of inorganic materials, other than fibrous fillers, to enhance their pigmenting or filling properties
- C09C3/04—Physical treatment, e.g. grinding, treatment with ultrasonic vibrations
- C09C3/041—Grinding
-
- 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
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/001—Pigment pastes, e.g. for mixing in paints in aqueous medium
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2004/00—Particle morphology
- C01P2004/60—Particles characterised by their size
- C01P2004/62—Submicrometer sized, i.e. from 0.1-1 micrometer
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
- C01P2006/00—Physical properties of inorganic compounds
- C01P2006/22—Rheological behaviour as dispersion, e.g. viscosity, sedimentation stability
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Structural Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Curing Cements, Concrete, And Artificial Stone (AREA)
Abstract
A thixotropic slurry is made by first mixing a dispersant (preferably 0.1 to 3%, based on the weight of slurry), a stabilizer (preferably 0.4 to 15%), and an aqueous carrier (preferably 12 to 77%), then mixing in a solid particulate pigment (preferably 20 to 70%) until the resulting mixture is uniform, and finally subjecting the mixture to high energy processing, e.g. milling, to reduce the pigment particles to a micron size range, preferably 0.5 to 40 microns.
Description
SPECIFICATION
Method of Producing Cement Colouring
Composition
This invention relates to a method of producing a colouring material for cementitious mixes used in making products such as cast concrete, extruded concrete, cement fibre glass, and cement asbestos.
Conventional cement or concrete colouring compositions comprise powders which are added
by hand or by a screw conveyor in their dry state to a wet concrete or cement mix in a mixing
apparatus. It is difficult to accurately add desired
amounts of such powders to the wet concrete mix and there is often waste of such colouring
material. Furthermore, with powders it is difficult to obtain a sufficient thorough mixing of the powders into the wet cement mix so as to achieve a homogeneous colour throughout the mixture.
Conventional methods also require the concrete or cement contractor to maintain large inventories of the colouring composition and involve certain health hazards as well.
It is highly desirable to have a system for colouring wet cement and concrete mixes by the addition of the colouring material in a liquid form to the mix, so that the colouring material may be added by liquid pumps to the wet concrete mix. In particular it is desirable to be able to produce a pigment suspension which will not settle out within a relatively short time.
The present invention provides a method of producing a colouring composition for a cementitious mix, comprising making a thixotropic slurry by the following steps: (a) forming a mixture of a dispersant and a stabilizer in an aqueous carrier; (b) mixing a solid particulate pigment into the mixture from step (a) until the resulting mixture is uniform; and (c) subjecting the mixture from step (b) to high energy processing which reduces the pigment particles to a micron size range.
Preferably, the following amounts of the dispersant, the stabilizer, the aqueous carrier, and the pigment are used, based on the weight of the slurry: dispersant, 0.1 to 3%; stabilizer, 0.4 to 15%; aqueous carrier, 12 to 77%; pigment, 20 to 70%.
The invention will be described further with reference to the following Examples and the accompanying drawing, whose sole Figure is a graph illustrating preferred ranges of viscosity plotted against time for three exemplary iron oxide pigments after they have been processed into slurries.
In the following description all percentages are by weight.
Example 1
A mixing tank having a slow speed or low energy agitator revolving at 80 to 200 rev/min is partially filied with 47.17% of water (based on the weight of slurry to be produced). A natural gum such as gum arabic in the amount of 5% is then added as well as 0.66% of a dispersant such as sodium laurate, which is a sodium salt of lauric acid sulphonate. At ambient temperatures, the water, dispersant, and stabilizer are premixed until all are dissolved. Then, while the mixer is still running, 47.17% of a pigment such as black iron oxide is added and the entire mixture is then mixed for about one hour, for example, until it is uniform and homogeneous, whereupon it will have a predetermined specific gravity.
Next, the material is pumped into a high speed or high energy mill such as a stone mill, for example, to reduce the particle size of the pigment component of the slurry down into the micron range. This can be checked by the use of a grinding "wedge" or other gauge. Preferably, the pigment particle size distribution in the resulting thixotropic slurry should include largest particles with a maximum dimension of about 40 microns, large particles whose average size is about 25 microns, smaller particles whose average size is in the 1-2 micron range, and smallest particles down to a minimum size of about 0.5 microns. If the particle distribution is generally higher than these ranges, the colouring strength of the slurry is adversely affected. If the sizes of the particles are generally below these ranges they may be washed out of dried concrete by normal weathering.
The procedure described above may also be applied to many other formulations such as are set forth in the following examples:
Example 2
Black Iron Oxide 47.17%
Water 47.73%
Gum Arabic 5.00%
Sodium Laurate 0.10% Example 3
Carbon Black 20.00%
Water 76.60%
Gum Arabic 0.4%
Ethylene Oxide Condensate 3.0%
Example 4
Carbon Black 25.0% Water 59.0%
Alginate L.V. 15.0% Sodium Laurate 1.0%
Example 5
Spanish Red Oxide 80.0%
Water 12.69% Gum Arabic 7.0%
Ethylene Oxide Condensate 0.4%
Example 6
Red Oxide (Natural) 60.00%
Water 30.00%
Gum Arabic 9.20%
Sodium Laurate 0.80%
Example 7
Red Oxide (Synthetic) 50.00%
Water 47.00%
Gum Arabic 2.80%
Sodium Laurate 0.20%
Example 8
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Gum Arabic 3.2% Sodium Laurate 0.3% Example 9
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Sodium Alginate (Manute RS) 3.2% Sodium Laurate 0.3% Example 10
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Carboxymethyl Cellulose
(CMC) High Viscosity
grade 3.2% Sodium Laurate 0.3%
Example 11
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Gum Arabic 3.4% Triethanolame 0.1% Example 12
Yellow Oxide (Synthetic) 47.00%
Water 49.5% Gum Guar 3.2% Sodium Laurate 0.3% Example 13
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Gum Tragacanth 3.2% Sodium Laurate 0.3% Example 14
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Locust Bean Gum 3.2% Sodium Laurate 0.3% Example 15
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Dextrine 3.2% Sodium Laurate 0.3% Example 16
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Potato Starch 3.2% Sodium Laurate 0.3% Example 17
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Polyvinyl Alcohol 3.2% Sodium Laurate 0.39/0 Example 18
Yellow Oxide (Synthetic) 47.00%
Water 49.5%
Polyvinyl Pyrolidone 3.2%
Sodium Laurate 0.3%
The dispersant helps the slurry to keep its suspended state for long periods of time, and they facilitate the incorporation of large amounts of
pigment into the slurry. They also tend to prevent flocculation of the pigment when the slurry is
added to a cement mix containing free calcium
ions.Less flocculation makes for more intense
colouring of the cement mix.
In each of the above examples the water may
be replaced by an aqueous solution of a freezing
point depressant in such an amount that the
slurry freezes only below a given subzero
temperature.
By way of example, in order to achieve a freezing point of-250C, any one of the following freezing point depressants can be used in the following percentages based on the quantity of
aqueous solution: magnesium sulphate 25%;
sodium sulphate 25%; ethylene glycol 15%: propylene glycol 17%; glycerol 20%; sorbitol 20%; ethyl alcohol 30%; methyl alcohol 33%; isopropyl alcohol 33%. Magnesium and sodium
sulphate have a slight retarding effect on the
curing of the cementitious products. The alcohols appear not to affect curing, even when used at
high concentrations, e.g. 8 to 10% based on the weight of the cementitious mix.
In practice the amount of freezing point depressant may be such that the slurry freezes only below -50C, preferably only below -1 00C.
The amount is preferably 5 to 35% based on the weight of the aqueous solution.
It has been found that without the freezing point depressant the storage life of the slurry is sometimes shorter than expected. It is believed that this is owing to the effect of low temperatures when storage extends into winter.
The inclusion of the freezing point depressant
brings an improvement in storage life which appears to be due not only to the lower freezing point but also to the fact that, if the slurry does freeze, the way in which it freezes (passing through a paste-like state) inhibits settling out.
It is important that the viscosity of the formulation be controlled so as to ensure that the formulation can be fluidized when being dispensed, thereby to optimize the mixing of the formulation with the cement or concrete components. The product is therefore checked as to its viscosity, which should fall substantially within the limits (measured in poise) as shown in the accompanying drawing. While the data shown in the graph just deals with iron oxides, the desirable viscosity ranges for other pigments will also fall within the maximum and minimum
ranges shown in the graph. The data plotted was determined by the use of a "Rotothinner" brand viscometer manufactured by ICI. This viscometer works by detecting mechanical shear, not by the detection of heat generation.
The colour quality of the slurry may be tested by adding to it a predetermined quantity of titanium dioxide (white) in the 3:1 to 5:1 ratio range. This measures the relative value of the colour, since a given sample may require a different amount of the colouring pigment to produce the same tint as another batch of the slurry.
Other usable stabilizers include active clays such as bentonite, kieselgur, or benagel, uncooked corn or wheat starch, water-soluble ceiluloses such as hydroxy ethyl cellulose or methyl cellulose, and polyvinyl pyrolidone.
Other usable dispersants include other fatty amines and alkylamines. Cationic surfactants, such as "Wetfix SE" (trade mark), are particularly suitable for compositions to be used for colouring cement asbestos.
Optionally, other substances may also be added to impart desired characteristics to the composition. For example, a small percentage, say 4 to 7%, of an anti-efflorescence agent such as barium carbonate can be added. Or small percentages (say about 2%) of water-repellent chemicals such as calcium stearate, aluminium stearate, or silicones can be added to the pre-mix of the dispersant and the stabilizer in the aqueous carrier.
The premixing step may be alternatively accomplished by using a hydraulic, variable speed cavitation mixer such as those marketed by
Torrance 8 Sons of Bristol, England, or by Cowles in the United States. Present cavitation mixers are, however, somewhat limited in processing capacity.
The reduction of the particle size of the original slurry by high energy processing may be done by mills other than the stone mill. Alternatively, a
Premier brand colloid mill manufactured by
Premier Colloid Mills or other types of comminuting apparatus may be employed. Stone mills may be those manufactured by Moorhouse in the United States or by Fryma in Switzerland.
Ball mills or rod mills have also been satisfactorily used, but they have the disadvantage of requiring more processing time. Attrition mills such as sand mills or pearl mills also are effective, but also usually take longer than high speed mills or colloid mills.
One of the main advantages of the present invention is that thixotropic slurries of various
main colours produced according to the present invention may be packaged in drums or other containers and the suspensions will not settle out for relatively long periods of time, i.e. of the order of 6 to 12 months. Thus, if the concrete or cement contractor wishes, he can keep perhaps 3 to 5 pigment slurries in individual drums, each slurry being operatively connected to a batching system which controls the amounts of the slurries to be added to the concrete mix. A charging pump
may be inserted into each drum of slurry
connected through a delivery tube to a metering container or tube. The tube may, for example, contain a first (higher) measuring probe connected to a batching control unit whose height is adjustable (or predetermined) depending upon the amount of slurry to be measured out.
Operation of the charging pump delivers the slurry to the metering tube until it touches the lower end of the first measuring probe whereupon a circuit is actuated which cuts off the pump. The charging pump for applying the slurry to the metering tube may be an air-operated positive displacement piston pump such as those marketed by Graco,
Inc. of Minneapolis, Minnesota. Then the contents of the metering tube start to be withdrawn from the metering tube by the action of a dispensing pump (controlled by the batching unit) and to be applied (with water) to a concrete mixer of any conventional type. When the level of the metered slurry falls below the lower end of a second probe coupled to the batching unit, a signal is generated which stops the dispensing pump.
If the contents of the slurry drum have not been used for excessive lengths of time, it may be advisable to insert a recycling valve branching off from the output of the charging pump and being connected to a recycling tube which returns to the drum. The return of the slurry back to the drum will produce a certain amount of agitation of the contents of the drum.
Instead of the batching system described
above, it is also possible to use a positive
displacement pump of the said Graco type or of the "Mono" brand type marketed by Mono Pumps
Ltd. of Great Britain. The latter pump is also
marketed in the United States under the "Moyno"
brand by Robbins and Meyers. The pump is set to
run for a timed period so that, since the rate of flow is known, the amount of pumping time required to produce a given volume can easily be calculated. The timers may be wired to the electric motor starters of the pumps.
Still another method is to pump the slurry around a continuous circuit via a three-way valve which is air or electrically operated. The valve is connected to a timer that can switch it from continuous circuit to injection by-pass, either straight into the mixing apparatus or indirectly, via a weighing scale, into the mixer so as to provide a double check on the quantity required for addition.
Claims (12)
1. A method of producing a colouring composition for a cementitious mix, comprising making a thixotropic slurry by the following steps:
(a) forming a mixture of a dispersant and a stabilizer in an aqueous carrier;
(b) mixing a solid particulate pigment into the mixture from step (a) until the resulting mixture is uniform: and
(c) subjecting the mixture from step (b) to high energy processing which reduces the pigment particles to a micron size range.
2. A method as claimed in claim 1, in which the following amounts of the dispersant, the stabilizer, the aqueous carrier, and the pigment are used, based on the weight of the slurry: dispersant, 0.1 to 3%; stabilizer, 0.4 to 15%; aqueous carrier, 12 to 77%; pigment, 20 to 70%.
3. A method as claimed in claim 1 or 2, in which the stabilizer comprises at least one of the following: active clays, natural products of the alginate group, hydrolysed starches, watersoluble celluloses, natural starches, synthetic polymers of the polyvinyl type, and water-soluble natural gums.
4. A method as claimed in any of claims 1 to 3, in which the pigment comprises at least one of the following: metallic oxides, metallic salts, and carbon black.
5. A method as claimed in any of claims 1 to 4, in which the pigment particle sizes are substantially within the range 0.5 to 40 microns.
6. A method as claimed in any of claims 1 to 5, in which the dispersant comprises at least one of the following: ethylene oxide condensates, fatty amines, alkylamines, and sulfonated soaps in the form of a metal derivative salt.
7. A method as claimed in any of claims 1 to 5, for producing a composition for colouring cement asbestos, in which the dispersant is a cationic surfactant.
8. A method as claimed in any of claims 1 to 7, in which the aqueous carrier is water.
9. A method as claimed in any of claims 1 to 7, in which the aqueous carrier contains a freezing point depressant in such an amount that the slurry freezes only below -50C.
10. A method as claimed in claim 9, in which the amount of freezing point depressant is such that the slurry freezes only below -1 00C.
11. A method as claimed in claim 9 or 10, in which the aqueous carrier contains 5 to 35% by weight of the freezing point depressant.
12. A method as claimed in any of claims 1 to 11, in which the freezing point depressant comprises an alcohol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7943385A GB2065157B (en) | 1979-12-17 | 1979-12-17 | Method of producing cement colouring composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB7943385A GB2065157B (en) | 1979-12-17 | 1979-12-17 | Method of producing cement colouring composition |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2065157A true GB2065157A (en) | 1981-06-24 |
GB2065157B GB2065157B (en) | 1983-08-24 |
Family
ID=10509898
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7943385A Expired GB2065157B (en) | 1979-12-17 | 1979-12-17 | Method of producing cement colouring composition |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2065157B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6204319B1 (en) | 1998-10-30 | 2001-03-20 | E.I. Du Pont De Nemours And Company | Aqueous coating compositions |
WO2003072659A1 (en) * | 2002-02-26 | 2003-09-04 | K.U. Leuven Research & Development | Method for reducing the size of metallic compound particles |
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 |
US7666307B2 (en) | 2003-08-26 | 2010-02-23 | K.U. Leuven Research & Development | Particle size reduction of bioactive compounds |
WO2010105165A1 (en) * | 2009-03-12 | 2010-09-16 | Sun Chemical Corporation | Polymer bound organic pigment and substrate composites and process for making |
-
1979
- 1979-12-17 GB GB7943385A patent/GB2065157B/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6204319B1 (en) | 1998-10-30 | 2001-03-20 | E.I. Du Pont De Nemours And Company | Aqueous coating compositions |
WO2003072659A1 (en) * | 2002-02-26 | 2003-09-04 | K.U. Leuven Research & Development | Method for reducing the size of metallic compound particles |
US7384560B2 (en) | 2002-02-26 | 2008-06-10 | K.U. Leuven Research & Development | Method for reducing the size of metallic compound particles |
US7666307B2 (en) | 2003-08-26 | 2010-02-23 | K.U. Leuven Research & Development | Particle size reduction of bioactive compounds |
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 |
WO2010105165A1 (en) * | 2009-03-12 | 2010-09-16 | Sun Chemical Corporation | Polymer bound organic pigment and substrate composites and process for making |
Also Published As
Publication number | Publication date |
---|---|
GB2065157B (en) | 1983-08-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PE20 | Patent expired after termination of 20 years |
Effective date: 19991216 |