Compositions: coating or plastic – Materials or ingredients – Pigment – filler – or aggregate compositions – e.g. – stone,...
Reexamination Certificate
2000-03-03
2002-01-29
Marcheschi, Michael (Department: 1755)
Compositions: coating or plastic
Materials or ingredients
Pigment, filler, or aggregate compositions, e.g., stone,...
C106S465000, C423S430000, C524S425000, C523S210000, C162S181100, C428S403000
Reexamination Certificate
active
06342100
ABSTRACT:
BACKGROUND OF THE INVENTION
The invention relates to a bimolecularly coated calcium carbonate, as well as to a method for the controlled surface treatment of calcium carbonate.
The use of finely ground limestone or precipitated calcium carbonate as a filler, for example, for rubber, plastics, paper or paints, is known. Likewise, it is known that the dispersibility of the calcium carbonate particles in or the affinity of the particles towards the substance or the mixture, to which the calcium carbonate is to be added as a filler, can be improved or increased by a surface treatment with, for example, fatty acids or their salts.
The German patent 958 830 describes a method for improving the properties of calcium carbonate, in which the calcium carbonate is ground in the presence of surface-active materials. In order to achieve complete coverage of the calcium carbonate particles, the amount of surface-active materials added can fluctuate appreciably. According to the German patent 958 830, the limits lie between 0.1 and 40% by weight, based on the amount of calcium carbonate.
From the German patent 38 01 649 or the German patent 39 00 054, it is known that compositions, which protect the subsoil and have improved flowability, can be produced if the fillers, especially calcium carbonate, are coated completely or partially with surface-active materials. These publications do not provide details concerning the degree of the partial surface coverage.
Coated calcium carbonate is required and used for different applications as a functional filler. The different applications also place different requirements on the coated calcium carbonate. These requirements are described, for example, by the liquid limit in the plasticizer mixture (Bingham method). Certain liquid limits have proven to be particularly suitable for the individual applications.
Based on the previously known methods for treating the surface calcium carbonate particles, it could be assumed that there is a relationship between the degree of coating and the liquid limit. A method for controlling the application properties, which utilizes this relationship, has not previously become known.
SUMMARY OF THE INVENTION
It is an object of the invention to provide a method for the preparation of coated calcium carbonate with a defined degree of coating and with defined properties.
Pursuant to the invention, this objective is accomplished owing to the fact that the required amount of coating agent is determined on the basis of the average particle diameter (dp) of the calcium carbonate. Accordingly, the application properties of the fillers can be controlled by the selective variation of particular diameters and/or of the degree of coating.
In particular, properties such as the liquid limit, viscosity, thixotropy, dispersibility or adhesion capability of mixtures can be controlled and affected by coated calcium carbonate as functional filler.
The calcium carbonate, which is treated pursuant to the invention, can be natural calcium carbonate or chalk or synthetic calcium carbonate, such as precipitated calcium carbonate, which has been ground dry or wet.
Usually, calcium carbonate is used as filler, which has an average particle diameter of not more than 50 &mgr;m and preferably of less than 20 &mgr;m and particularly of less than 5 &mgr;m. Particles with an average particle size of 0.005 to 5 &mgr;m and particularly of 0.01 to 1 &mgr;m are preferred.
Within the scope of the invention, coating agents are materials, which can be held by surface activity on the calcium carbonate particles.
DESCRIPTION OF PREFERRED EMBODIMENTS
In one embodiment of the invention, saturated and/or unsaturated carboxylic acids, such as fatty acids, substituted fatty acids, their salts or fatty alcohols, to name but a few suitable materials, are used as coating agents. In a preferred embodiment, C
2
to C
32
fatty acids and preferably C
14
to C
22
fatty acids, such as stearic acid, or the alkali or ammonium salts of the corresponding fatty acids are used as coating agents.
The calcium carbonate is brought into contact with the coating agent in a known manner. The coating agent is dispersed or emulsified in liquid or solid form, preferably as an emulsion with the dispersed calcium carbonate, for example, during the grinding process or during and/or after the precipitation, the coating agent adhering to the surface of the calcium carbonate.
In one embodiment, the treatment of the calcium carbonate with the surface-active material takes place in emulsified form in an aqueous system. At the same time, it surprisingly was found that the calcium carbonate has a bimolecular coating, that is, a double layer. The space required by stearic acid as coating agent, that is, how much calcium carbonate particle surface area must be present, was calculated by known methods. The degree of coverage was determined by ESCA measurements and compared with the space required. By these means, it was determined that a double layer must be present. It was furthermore possible to determine that 20 to 60% of the crystalline surface of the calcium carbonate particles are coated in the form of a double layer.
The mechanism of forming the double layer can be explained in the following manner:
In a mixture of water, sodium hydroxide and stearic acid, spherical micelles of the sodium stearate are formed. This emulsion is brought into contact with the calcium carbonate, for example, by mixing a suspension of calcium carbonate with the emulsion.
The micelles approach the calcium carbonate surface and contact this surface at a point, a salt-exchange reaction taking place.
By deformation of the micelles, a constantly increasing number of sodium stearate ions contact the calcium carbonate surface. Since the micelles do not open up and, instead, are only deformed, the described double layer is formed.
The space required by a stearate head group is about 20 Å. For example, calcium carbonate, with a BET surface area of 21 m
2
, is coated with 4.8% of stearate. This corresponds to 100% coverage in the case of a monolayer. ESCA measurements show that 49% of the carbonate surface, based on the total surface area, is covered and, moreover, in the form of a double layer.
The liquid limit according to Bingham in a plasticizer mixture is usually given as a typical characteristic of the suitability of calcium carbonates as a filler.
It was found that the ratio of coated to uncoated surface affects the liquid limit.
The degree of coating of the calcium carbonate also varies depending on the nature and amount of the coating agent. The liquid limit in the plasticizer mixture is therefore determined in a known manner and, after that, related to the degree of coating.
By using the method of the invention, it is possible to control the degree of coating so precisely, that the coated calcium carbonate can be made available in the quality required with a high degree of reproducibility and in an efficient manner.
In order to be able to determine the amount of coating agent, which must be used in order to obtain the desired properties, the average particular diameter of the calcium carbonate crystals is first of all determined. Different methods are known for determining the particle size.
Based on the method of Blaine, the average particle diameter (dp) is determined by measuring the air permeability of a compressed calcium carbonate tablet.
The particle surface area, required for determining the necessary amount of coating agent, is obtained from the following equation:
average specific surface area of the particles, assuming that they are spheres=
4
π
(
dp
/
2
)
2
(
4
/
3
)
π
(
dp
/
2
)
3
×
d
The density (d) of calcitic calcium carbonate is 2.71×10
6
g/m
3
and of aragonitic calcium carbonate 2.93×10
6
g/m
3
.
Accordingly, the average specific surface area of the particles, assuming that they are spheres, is 2.21/dp (m
2
/g) for calcitic calcium carbonate and 2.05/dp (m
2
/g) for aragonitic calcium carbonate. The amount of coating agent, required for t
Dillenburg Helmut
Nover Christoph
Crowell & Moring LLP
Marcheschi Michael
Solvay Soda Deutschland GmbH
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