Compositions: coating or plastic – Materials or ingredients – Pigment – filler – or aggregate compositions – e.g. – stone,...
Reexamination Certificate
1997-11-28
2003-10-14
Koslow, C. Melissa (Department: 1755)
Compositions: coating or plastic
Materials or ingredients
Pigment, filler, or aggregate compositions, e.g., stone,...
C106S415000, C106S403000, C106S404000, C252S520100
Reexamination Certificate
active
06632276
ABSTRACT:
BACKGROUND OF THE INVENTION
The invention relates to electrically conductive pigments which have, as a conductive layer on a substrate, a tin oxide layer doped with phosphorus.
In many areas of industry there is a need for conductive pigments with which, for example, electrically conductive plastics, paints, coatings, fibers or the like which provide shielding from antistatic or electromagnetic waves can be prepared. Conductive carbon black is employed in large amounts for this purpose, but because of its high absorption of light, it cannot be employed for pale or colored coatings.
Another disadvantage is the high absorption of carbon black in the IR range, which, for example, leads to an often undesirable warming of the coated objects under solar irradiation.
EP 373,575 discloses conductive platelet-shaped pigments which have, as a conductive layer, a tin oxide doped with antimony, a thin layer of silicon dioxide being located between the conductive layer and the substrate. The application of an additional layer to the substrate means a considerable increased outlay during preparation and leads to the pigment becoming more expensive.
DE 42 13 747 A1 (corresponding to U.S. Pat. No. 5,350,448) describes conductive pigments which have, as the conductive layer on a substrate, a tin and/or titanium oxide layer doped with halogen.
However, the conductive pigments from the prior art are not sufficiently opaque and are therefore not suitable for the production of decorative coatings.
Furthermore, the pigments have conductivity values which do not meet the high requirements in this area.
There was therefore a need for stable electrically conductive pigments which are opaquely pale or even colored and, in addition to conductivity, impart to the coatings or plastics a decorative appearance.
SUMMARY OF THE INVENTION
Surprisingly, it has now been found that coating substrates with a tin oxide layer doped with phosphorus leads to decorative conductive pigments which have none of the above-mentioned disadvantages.
The fact that tin oxide powder doped with phosphorus is electrically conductive, is already known from EP-A1 582,371. However, coating of substrates with a tin oxide layer doped with phosphorus is not described in the prior art.
The invention thus relates to conductive pigments which are distinguished by the fact that a substrate is coated with a conductive layer, the conductive layer being a tin oxide layer doped with phosphorus.
The invention furthermore relates to a process for the preparation of the conductive pigments according to the invention, which is characterized in that an aqueous substrate suspension is prepared and a hydrolyzable tin salt solution and an aqueous phosphorus compound are added, the pH of the substrate suspension being kept in a range which effects hydrolysis of the tin salt by simultaneous addition of a base or an acid, and the substrate coated in this manner is separated off, washed, dried and calcined at temperatures of 400-1100° C. with exclusion of oxygen.
Substrates which can be employed are either platelet-shaped or spherical particles. All known platelet-shaped carrier materials, such as, for example, metals, metal oxides, mica pigments and synthetic platelets, can be coated by the process according to the invention. Examples of these are naturally occurring or synthetic mica, other laminar silicates, such as talc, kaolin or sericite, or other comparable materials, platelet-shaped iron oxide, aluminum platelets, bismuth oxychloride, SiO
2
flakes, glass flakes or synthetic ceramic flakes.
Since no high gravity forces are required in the process, the process is also outstandingly suitable for coating pearl luster pigments, for example mica coatings with colored or colorless metal oxides, such as TiO
2
, Fe
2
O
3
, SnO
2
, Cr
2
O
3
, ZnO and other metal oxides, by themselves or as a mixture in a uniform layer or in successive layers. These pigments are known, for example, from German Patents and Patent Applications 14 67 468, 19 59 998, 20 09 566, 2 14 545, 22 15 191, 2 44 298, 23 13 331, 25 22 572, 32 11 602 and 32 35 017 and are commercially obtainable, for example under the trade name Iriodin® from E. Merck, Darmstadt.
The spherical particles can consist be for example, SiO
2
or metal oxides, such as, for example, Fe
2
O
3
, TiO
2
, MgTiO
3
, CaTiO
3
, BaTiO
3
, SrTiO
3
, Al
2
O
3
or BaSO
4
, CaSO
4
, or CaCO
3
. Preferred spherical particles are Al
2
O
3
, BaSO
4
or SiO
2
.
The particles have an average diameter of less than 200 &mgr;m, and in particular not more than 50 &mgr;m. Platelet-shaped substrates extend less than 500 &mgr;m in the main dimension, in particular less than 250 &mgr;m, and their thickness is less than 10 &mgr;m, preferably not more than 5 &mgr;m, and in particular in the range from 0.1 to 1 &mgr;m. The ratio of the extension in the main dimension to the thickness (aspect ratio) of the platelet-shaped substrates is more than 3, and in particular more than 5.
The substrates to be coated can also be a mixture of platelet-shaped and spherical particles, the platelet-shaped:spherical ratio preferably being in the range from 80:20 to 20:80, and in particular 50:50.
According to the invention, the substrates are suspended in water, and the solution of a water-soluble tin salt and a water-soluble phosphorus compound is added, preferably at elevated temperature and at a suitable pH, the pH being kept in the suitable range, if appropriate, by simultaneous addition of an acid or base.
The industrially readily accessible bases, such as, for example, NaOH, KOH or ammonia, and, as acids, dilute mineral acids are expediently used. Since the bases and acids serve only to change the pH, their nature is not critical, so that other acids and bases can also be employed.
Suitable tin salts are preferably the 2- and 4-valent halides, sulfates or nitrates, preferably the halides, and in particular the chlorides. A tin salt solution comprising SnCl, and SnCl
2
, the ratio of Sn
IV
to Sn
II
being in the range from 90:10 to 10:90, in particular 80:20 to 60:40, is particularly preferred, and solutions which comprise only tin(IV) salts are furthermore preferred. The tin salts can also be added in solid form to the aqueous substrate suspension.
Suitable phosphorus compounds are the phosphorus trihalides, phosphoryl halides and the oxygen acids of phosphorus, as well as sodium phosphates. The readily accessible and inexpensive phosphoric acid or sodium phosphate is preferably employed.
A conductive layer of tin oxide doped with phosphorus, the layer being applied in an amount of about 25-100% by weight, based on the substrate, in particular in an amount of 50-75% by weight, is preferred. Although larger amounts are also possible per se, no further increase in conductivity is thereby achieved, and the pigments become increasingly darker. The content of tin oxide is typically 20-70% by weight based on the total pigment. The content of phosphorus in the conductive layer, based on the tin, is 0.1-20 atom %, preferably 1-10 atom %, and in particular 2-8 atom %. If the phosphorus content is too low, high conductivities cannot be achieved, while if the phosphorus content is too high, the pigments become increasingly paler and the conductivity decreases drastically.
The desired homogeneous distribution of tin and phosphorus in the conductive layer can be achieved without problems by metering the tin compounds and phosphorus compounds in water, either together in one solution or in two separate solutions, continuously and in the predetermined mixing ratio into the substrate suspension at a suitable pH of about 1 to 5 and a suitable temperature of about 50 to 90° C. such that in each case hydrolysis and deposition on the substrate take place immediately.
Any acid or base can be employed to precipitate the metal salts. The optimum concentrations and pH values can be determined by routine experiments. The pH once established for the precipitation is usually retained throughout the entire precipitation in order to achieve uniform pigments.
When the coating op
Koslow C. Melissa
Merck Patent Gesellschaft mit beschrankter Haftung
Millen White Zelano & Branigan P.C.
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