Effect pigments

Abstract

Temperature-stable effect pigments based on multicoated flake-form substrates, and the use thereof in paints, coatings, printing inks, plastics and in particular in glazes, enamels, ceramic or glass-like materials.

Claims

1. An effect pigment based on a multicoated flake-form substrate, wherein a surface of the substrate has at least one layer sequence comprising: (A) a base layer comprising a high-refractive-index coating having a refractive index of n1.8; (B) a pseudobrookite layer, which may optionally be doped with one or more oxides in amounts of 10% by weight, based on the weight of layer (B); (C) a low-refractive-index layer having a refractive index of n<1.8; (D) a high-refractive-index layer having a refractive index of n>1.8 and consisting of at least 2 different colorless metal-oxide layers; (E) a pseudobrookite layer, which may optionally be doped with one or more oxides in amounts of 10% by weight, based on the weight of layer (E); and optionally (F) an outer protective layer; wherein layers (C) and (D) have a total combined layer thickness of 50-115 nm, separating layer (B) from layer (E), and wherein no phase reactions occur between the individual layers (A) to (F), even at a temperature that is above 900 C .

2. The effect pigment of claim 1, wherein the flake-form substrate is selected from the group consisting of phyllosilicate, BiOCl, SiC, TiC, WC, B.sub.4C, BN, graphite, TiO.sub.2, Fe.sub.2O.sub.3 flakes, doped or undoped Al.sub.2O.sub.3 flakes, doped or undoped glass flakes, doped or undoped SiO.sub.2 flakes, and mixtures thereof.

3. The effect pigment of claim 1, wherein the phyllosilicate comprises natural mica, synthetic mica, kaolin or talc.

4. The effect pigment of claim 1, wherein layer (A) comprises one or more metal oxides.

5. The effect pigment of claim 4, wherein the metal oxide of layer (A) is selected from the group consisting of TiO.sub.2, Fe.sub.2O.sub.3, Fe.sub.3O.sub.4, Fe(O)OH, BiOCI, Cr2O3, ZnO, Ce.sub.2O.sub.3, ZrO.sub.2, SnO.sub.2, Co.sub.2O.sub.3, Ti suboxides, titanium oxynitrides, titanium nitride, CoO, Co.sub.2O.sub.3, Co.sub.3O.sub.4, VO.sub.2, V.sub.2O.sub.3, NiO, WO.sub.3, MnO, Mn.sub.2O.sub.3, and mixtures of the said oxides.

6. The effect pigment of claim 1, wherein layer (B) and/or layer (E) is doped with one or more oxides or oxide mixtures selected from the group consisting of Al.sub.2O.sub.3, Ce.sub.2O.sub.3, B.sub.2O.sub.3, ZrO.sub.2, SnO.sub.2, Cr.sub.2O.sub.3, CoO, Co.sub.2O.sub.3, Co.sub.3O.sub.4, and Mn2O.sub.3.

7. The effect pigment of claim 1, wherein layer (C) comprises SiO.sub.2, MgO*SiO.sub.2, CaO*SiO.sub.2, Al.sub.2O.sub.3*SiO.sub.2, B.sub.2O.sub.3*SiO.sub.2, or of a mixture of the said compounds.

8. The effect pigment of claim 1, wherein layer (D) comprises at least two metal-oxide layers, where the metal oxides are selected from the group consisting of SnO.sub.2, TiO.sub.2, Al.sub.2O.sub.3, Cr.sub.2O.sub.3, Fe.sub.2O.sub.3, and mixtures thereof.

9. The effect pigment of claim 1, wherein layer (D) comprises metal-oxide layers (D1) and (D2): (D1) SnO.sub.2 layer: (D2) TiO.sub.2 layer.

10. The effect pigment of claim 1, wherein layer (D) comprises metal-oxide layers (D1), (D2) and (D3): (D1) Al.sub.2O.sub.3 layer; (D2) TiO.sub.2 layer; and (D3) Al.sub.2O.sub.3 layer.

11. The effect pigment of claim 1, wherein layer (D) comprises metal-oxide layers (D1), (D2) and (D3): (D1) SnO.sub.2 layer (D2) TiO.sub.2 layer; and (D3) SnO.sub.2 layer.

12. The effect pigment of claim 1, wherein layers (B) and (E) have an equal layer thicknesses.

13. The effect pigment of claim 1, wherein the outer protective layer (F) comprises SnO.sub.2.

14. The effect pigment of claim 1, having at least one of the following structures: substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite; substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite; or substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite.

15. A paint, coating, printing ink, security printing ink, plastic, ceramic material, ceramic colour, glaze, engobe, enamel, glass, absorber for laser marking of plastics and papers, cosmetic formulation, pigment preparation, ordry preparation comprising the effect pigment of claim 1.

16. A formulation comprising the effect pigment of claim 1.

17. The formulation of claim 16, comprising the effect pigment and at least one constituent selected from the group consisting of absorbents, astringents, antimicrobial substances, antioxidants, antiperspirants, antifoaming agents, antidandruff active compounds, antistatics, binders, biological additives, bleaches, chelating agents, deodorisers, emollients, emulsifiers, emulsion stabilisers, dyes, humectants, film formers, fillers, fragrances, flavours, insect repellents, preservatives, corrosion-protection agents, cosmetic oils, solvents, oxidants, plant constituents, buffer substances, reducing agents, surfactants, propellant gases, opacifiers, UV filters, UV absorbers, denaturing agents, aloe vera, avocado oil, coenzyme Q10, green tea extract, viscosity regulators, perfume, inorganic pigments, metal pigments, ceramic pigments, functional pigments, ceramic colour bodies, functional pigments, and vitamins.

Description

DETAILED DESCRIPTION

(1) Suitable base substrates for the effect pigments according to the invention are semitransparent and transparent flake-form substrates. Preferred substrates are phyllosilicate flakes, SiC, TiC, WC, B.sub.4C, BN, graphite, TiO.sub.2 and Fe.sub.2O.sub.3 flakes, doped or undoped Al.sub.2O.sub.3 flakes, doped or undoped glass flakes, doped or undoped SiO.sub.2 flakes, TiO.sub.2 flakes, BiOCl and mixtures thereof. From the group of the phyllosilicates, particular preference is given to natural and synthetic mica flakes, muscovite, talc and kaolin. The synthetic mica used as substrate is preferably fluorophlogopite or Zn phlogopite.

(2) The glass flakes can consist of all types of glass known to the person skilled in the art, so long as they are temperature-stable in the firing range used. Suitable glasses are, for example, quartz, A glass, E glass, C glass, ECR glass, recycled glass, alkali metal borate glass, alkali metal silicate glass, borosilicate glass, Duran glass, laboratory equipment glass or optical glass.

(3) The refractive index of the glass flakes is preferably 1.45-1.80, in particular 1.50-1.70. The glass substrates particularly preferably consist of C glass, ECR glass or borosilicate glass.

(4) Synthetic substrate flakes, such as, for example, glass flakes, SiO.sub.2 flakes, Al.sub.2O.sub.3 flakes, may be doped or undoped. If they are doped, the doping is preferably Al, N, B, Ti, Zr, Si, In, Sn or Zn or mixtures thereof. Furthermore, further ions from the group of the transition metals (V, Cr, Mn, Fe, Co, Ni, Cu, Y, Nb, Mo, Hf, Sb, Ta, W) and ions from the group of the lanthanides can serve as dopants.

(5) In the case of Al.sub.2O.sub.3, the substrate is preferably undoped or doped with TiO.sub.2, ZrO.sub.2 or ZnO. The Al.sub.2O.sub.3 flakes are preferably corundum. Suitable Al.sub.2O.sub.3 flakes are preferably doped or undoped -Al.sub.2O.sub.3 flakes, in particular -Al.sub.2O.sub.3 flakes doped with TiO.sub.2 or ZrO.sub.2.

(6) If the substrate is doped, the proportion of the doping is preferably 0.01-5% by weight, in particular 0.10-3% by weight, based on the substrate.

(7) The size of the base substrates is not crucial per se and can be matched to the particular application. In general, the flake-form substrates have a thickness between 0.05 and 5 m, in particular between 0.1 and 4.5 m.

(8) It is also possible to employ substrates having different particle sizes. Particular preference is given to a mixture of mica fractions of mica N (10-60 m), mica F (5-20 m) and/or mica M (<15 m). Preference is furthermore given to N and S fractions (10-130 m) and F and S fractions (5-130 m).

(9) Typical examples of particle-size distributions (measured using a Malvern Mastersizer 2000):

(10) D.sub.10: 1-50 m, in particular 2-45 m, very particularly preferably 5-40 m

(11) D.sub.50: 7-275 m, in particular 10-200 m, very particularly preferably 15-150 m

(12) D.sub.90: 15-500 m, in particular 25-400 m, very particularly preferably 50-200 m.

(13) In this patent application, high-refractive-index means a refractive index of 1.8, while low-refractive-index means a refractive index of <1.8.

(14) The layer sequence (A)-(E) or (A)-(F) of the effect pigment according to the invention is essential for the stability of the pigment and the optical properties.

(15) Layer (A) is a high-refractive-index layer having a refractive index of n1.8, preferably n2.0. Layer (A) may be colourless or absorbent in the visible wave light. Layer (A) preferably consists of metal oxides or metal-oxide mixtures. The metal oxide is preferably selected from the group TiO.sub.2, ZrO.sub.2, ZnO, SnO.sub.2, Cr.sub.2O.sub.3, Ce.sub.2O.sub.3, BiOCl; Fe.sub.2O.sub.3, Fe.sub.3O.sub.4, FeO(OH), Ti sub-oxides (partly reduced TiO.sub.2 having oxidation states from <4 to 2 and lower oxides, such as, for example, Ti.sub.3O.sub.5, Ti.sub.2O.sub.3 up to TiO), titanium oxynitrides and titanium nitride, CoO, Co.sub.2O.sub.3, Co.sub.3O.sub.4, VO.sub.2, V.sub.2O.sub.3, NiO, WO.sub.3, MnO, Mn.sub.2O.sub.3 or mixtures of the said oxides. Layer (A) preferably consists of TiO.sub.2, Fe.sub.2O.sub.3, Cr.sub.2O.sub.3 or SnO.sub.2.

(16) Layer (A) preferably has layer thicknesses of 1-15 nm, in particular of 1-10 nm and very particularly preferably of 1-5 nm.

(17) The pseudobrookite layers (B) and (E) may be identical or different. The layers are preferably identical in terms of composition. The pseudobrookite layers preferably consist entirely of Fe.sub.2TiO.sub.5. However, the Fe.sub.2TiO.sub.5 may be slightly super- or substoichiometric due to slight variations of the Fe/Ti ratio and resultant lattice vacancies.

(18) The layers can be produced by simultaneous addition and precipitation of an Fe-containing salt solution and a Ti-containing salt solution or by co-precipitation from a single solution containing Fe and Ti salts.

(19) The pseudobrookite layers should preferably consist of 100% of crystalline pseudobrookite.

(20) Layers (B) and (E) and may optionally additionally be doped with one or more oxides or oxide mixtures, preferably metal oxides, in order to increase the stability and/or tinting strength. The oxides are preferably selected from the group Al.sub.2O.sub.3, Ce.sub.2O.sub.3, B.sub.2O.sub.3, ZrO.sub.2, SnO.sub.2, Cr.sub.2O.sub.3, CoO, Co.sub.2O.sub.3, Co.sub.3O.sub.4, Mn.sub.2O.sub.3. The proportion by weight of the oxide or oxide mixture in the pseudobrookite layer is preferably not more than 5% by weight and is in particular in the range 1-5% by weight, very particularly preferably 1-3% by weight, based on layer (B) or layer (E).

(21) Layers (B) and (E) preferably each, independently of one another, have layer thicknesses in the range 60-120 nm, in particular 70-110 nm, and very particularly preferably 80-100 nm.

(22) It is particularly important for the stability of the effect pigments according to the invention that layers (B) and (E) are separated from one another by a separation layer (C) and a separation layer (D). The distance between layers (B) and (E) should preferably be 40-100 nm, in particular 45-90 nm and very particularly preferably 50-80 nm.

(23) The low-refractive-index layer (C) having a refractive index of n<1.8, preferably n<1.7, preferably consists of SiO.sub.2, MgO*SiO.sub.2, CaO*SiO.sub.2, Al.sub.2O.sub.3*SiO.sub.2, B.sub.2O.sub.3*SiO.sub.2 or of a mixture of the said compounds. Furthermore, the silicate layer may be doped with further alkaline-earth metal or alkali-metal ions. Layer (C) is preferably a silicate layer. Layer (C) very particularly preferably consists of doped or undoped SiO.sub.2.

(24) Layer (C) preferably has layer thicknesses of 40-90 nm, in particular of 40-70 nm and very particularly preferably of 50-60 nm.

(25) The high-refractive-index coating of layer (D) having a refractive index of n1.8, preferably n2.0, consists of at least two colourless metal-oxide layers. Layer (D) preferably consists of 2 or 3 colourless metal-oxide layers. The metal oxides are preferably selected from the group SnO.sub.2, TiO.sub.2, Al.sub.2O.sub.3, Fe.sub.2O.sub.3, Cr.sub.2O.sub.3 or mixtures thereof.

(26) The coating of layer (D) preferably consists of metal-oxide layers (D1) and (D2)

(27) (D1) SnO.sub.2 layer

(28) (D2) TiO.sub.2 layer

(29) or

(30) of metal-oxide layers (D1), (D2) and (D3)

(31) (D1) Al.sub.2O.sub.3 layer

(32) (D2) TiO.sub.2 layer

(33) (D3) Al.sub.2O.sub.3 layer

(34) or

(35) (D1) SnO.sub.2 layer

(36) (D2) TiO.sub.2 layer

(37) (D3) SnO.sub.2 layer.

(38) The coating of layer (D) preferably has layer thicknesses of 10-25 nm, in particular of 11-21 nm and very particularly preferably of 12-17 nm. The sum of all layer thicknesses of the individual metal-oxide layers (D1), (D2), (D3) and any further layers of the coating of layer (D) should not exceed 25 nm.

(39) In order that layers (C) and (D) are able to act as separation layers and thus contribute to the reduced phase reaction between the individual pseudobrookite layers (B) and (E), the total layer thickness of layers (C) and (D) should not exceed the thickness range of 120 nm and should preferably be in the range 50-115 nm, in particular 51-91 nm and very particularly preferably 62-77 nm.

(40) If layer (A) or (D) consists of TiO.sub.2, the TiO.sub.2 can be in the rutile or anatase modification.

(41) Particularly preferred effect pigments have the following structure: substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2 substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2 substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite substrate+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite

(42) Very particularly preferred effect pigments have the following layer structure: natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2 natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2 natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite natural mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2 synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2 synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite synthetic mica flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2 Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2 Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite Al.sub.2O.sub.3 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Fe.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Cr.sub.2O.sub.3+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Fe.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Cr.sub.2O.sub.3+pseudobrookite+MgO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Fe.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Cr.sub.2O.sub.3+pseudobrookite+CaO*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Fe.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+Cr.sub.2O.sub.3+pseudobrookite+Al.sub.2O.sub.3*SiO.sub.2+SnO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+TiO.sub.2+SnO.sub.2+pseudobrookite+SnO.sub.2 SiO.sub.2 flakes+TiO.sub.2+pseudobrookiteSiO.sub.2+SnO.sub.2+TiO.sub.2+pseudobrookite+SnO.sub.2 SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Fe.sub.2O.sub.3+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+SnO.sub.2+Cr.sub.2O.sub.3+SnO.sub.2+pseudobrookite SiO.sub.2 flakes+TiO.sub.2+pseudobrookite+SiO.sub.2+Al.sub.2O.sub.3+TiO.sub.2+Al.sub.2O.sub.3+pseudobrookite,

(43) where the SiO.sub.2 and Al.sub.2O.sub.3 flakes may be either doped or undoped. The Al.sub.2O.sub.3 flakes are preferably doped. The SiO.sub.2 flakes are preferably undoped.

(44) The metal-oxide layer(s) are preferably applied by wet-chemical methods, it being possible to use the wet-chemical coating methods developed for the preparation of pearlescent pigments; methods of this type are described, for example, in U.S. Pat Nos. 3,087,828, 3,087,829, 3,553,001, DE 14 67 468, DE 19 59 988, DE 20 09 566, DE 22 14 545, DE 22 15 191, DE 22 44 298, DE 23 13 331, DE 25 22 572, DE 31 37 808, DE 31 37 809, DE 31 51 343, DE 31 51 354, DE 31 51 355, DE 32 11 602, DE 32 35 017, DE 196 18 568, EP 0 659 843, or also in further patent documents and other publications known to the person skilled in the art.

(45) In the case of wet coating, the substrate flakes are suspended in water, and one or more hydrolysable metal salts are added at a pH which is suitable for hydrolysis, which is selected so that the metal oxides or metal oxide hydrates are precipitated directly onto the flakes without secondary precipitations occurring. The pH is usually kept constant by simultaneous metered addition of a base and/or acid. The effect pigments are subsequently separated off, washed and dried and optionally calcined, where the calcination temperature can be optimised with respect to the coating present in each case. In general, the calcination temperatures are between 250 and 1000 C., preferably between 350 and 900 C. If desired, the pigment can be separated off, dried and optionally calcined after the application of individual coatings and then re-suspended again for the precipitation of the further layers.

(46) For the application of an SiO.sub.2 layer, the process described in DE 196 18 569 is preferably used. For the production of the SiO.sub.2 layer, sodium water-glass solution or potassium water-glass solution is preferably employed.

(47) Furthermore, the coating can also be carried out by gas-phase coating in a fluidised-bed reactor, where, for example, the processes proposed for the preparation of pearlescent pigments in EP 0 045 851 and EP 0 106 235 can be used correspondingly.

(48) The hue of the pigments can be varied in broad limits by different choice of the coating amounts or of the resultant layer thicknesses. Fine tuning for a certain hue can be achieved beyond the pure choice of amounts by approaching the desired colour with visual or measurement technology control.

(49) In order to increase the light, water and weather stability, it is frequently advisable to subject the effect pigment according to the invention, depending on the area of application, to inorganic or organic post-coating or post-treatment (layer (F)). Suitable post-coatings or post-treatments are, for example, the methods described in German patent 22 15 191, DE-A 31 51 354, DE-A 32 35 017 or DE-A 33 34 598. This post-coating further increases the chemical and photochemical stability or simplifies handling of the effect pigment, in particular incorporation into various media. In order to improve the wettability, dispersibility and/or compatibility with the user media, functional coatings of SnO.sub.2, Al.sub.2O.sub.3 or ZrO.sub.2 or mixtures thereof can be applied to the pigment surface. Furthermore, organic post-coatings are possible, for example with silanes, as described, for example, in EP 0090259, EP 0 634 459, WO 99/57204, WO 96/32446, WO 99/57204, U.S. Pat. Nos. 5,759,255, 5,571,851, WO 01/92425 or in J. J. Ponje, Philips Technical Review, Vol. 44, No. 3, 81 ff. and P. H. Harding J. C. Berg, J. Adhesion Sci. Technol. Vol. 11 No. 4, pp. 471-493. Layer (F) is preferably a layer of SnO.sub.2.

(50) Coating(s) in this patent application are taken to mean the complete covering/sheathing of the flake-form substrates.

(51) The effect pigments according to the invention have increased temperature and heat stability compared with the unstabilised effect pigments. The stabilised effect pigments can be incorporated without problems into engobes and glazes. The glazes can be matt to glossy, or transparent to opaque, depending on the desired effect.

(52) The effect pigments according to the invention are furthermore suitable for the preparation of flowable pigment preparations and dry preparations, in particular for printing inks and paints, preferably automotive paints, consisting of the pigments according to the invention, binders and optionally one or more additives.

(53) The effect pigment according to the invention is compatible with a multiplicity of colour systems, Pref from the area of paints, coatings and printing inks. For the preparation of printing inks for, for example, gravure printing, flexographic printing, offset printing, offset overprint varnishing, a multiplicity of binders, in particular water-soluble types, is suitable, as marketed, for example, by BASF, Marabu, Prll, Sericol, Hartmann, Gebr. Schmidt, Sicpa, Aarberg, Siegwerk, GSB-Wahl, Follmann, Ruco or Coates Screen INKS GmbH. The printing inks can be built up on a water basis or solvent basis.

(54) The effect pigment according to the invention is suitable for decorative cosmetics and personal care applications, such as, for example, nail varnishes, lipsticks, compact powders, gels, lotions, soaps, toothpastes, body lotions, emotions, soaps, shampoos, BB creams, CC creams, make-up, foundations, mascara, hair, eyelash and eyebrow products, etc., but also in paints, in industrial coatings and powder coatings, and in plastics and in ceramics.

(55) In decorative cosmetics, the effect pigment according to the invention is preferably employed in concentrations of 0.5-25% by weight, in particular 1-20% by weight, and very particularly preferably 1-10% by weight, based on the formulation. In the case of cosmetic formulations for personal care applications, the effect pigment according to the invention is preferably employed in concentrations of 0.1-5% by weight, and very particularly preferably 0.5-4% by weight, based on the formulation.

(56) It goes without saying that, for the various applications, the effect pigment according to the invention can also advantageously be employed in a mixture with, for example, metal-effect pigments, for example based on iron flakes or aluminium flakes; pearlescent pigments based on metal-oxide-coated synthetic mica flakes, natural mica flakes, glass flakes, Al.sub.2O.sub.3 flakes, Fe.sub.2O.sub.3 flakes or SiO.sub.2 flakes; absorption pigments; goniochromatic pigments; multilayered pigments (preferably containing 2, 3, 4, 5 or 7 layers) based on metal-oxide-coated synthetic mica flakes, natural mica flakes, glass flakes, Al.sub.2O.sub.3 flakes, Fe.sub.2O.sub.3 flakes or SiO.sub.2 flakes; organic dyes; organic pigments; inorganic pigments, such as, for example, transparent and opaque white, coloured and black pigments; in particular temperature-stable ceramic pigments; flake-form iron oxides; carbon black; ceramic colour bodies; functional pigments, for example IR-reflective or electroconductive pigments.

(57) The effect pigment according to the invention can be mixed in any ratio with commercially available pigments and/or further commercially available fillers.

(58) Commercially available fillers which may be mentioned are, for example, natural and synthetic mica, nylon powder, pure or filled melamine resins, talc, glasses, kaolin, oxides or hydroxides of aluminium, magnesium, calcium, zinc, BiOCl, barium sulfate, calcium sulfate, calcium carbonate, magnesium carbonate, carbon, boron nitride and physical or chemical combinations of these substances. There are no restrictions regarding the particle shape of the filler. In accordance with requirements, it can be, for example, flake-form, spherical or needle-shaped.

(59) The effect pigment according to the invention can of course also be combined in the formulations with cosmetic raw materials and assistants of any type. These include, inter alia, oils, fats, waxes, film formers, preservatives and assistants which generally determine the applicational properties, such as, for example, thickeners and rheological additives, such as, for example, bentonites, hectorites, silicon dioxides, Ca silicates, gelatins, high-molecular-weight carbohydrates and/or surface-active assistants, etc.

(60) The formulation comprising the effect pigment according to the invention can belong to the lipophilic, hydrophilic or hydrophobic type. In the case of heterogeneous formulations having discrete aqueous and non-aqueous phases, the effect pigment according to the invention may be present in only one of the two phases in each case or also distributed over both phases.

(61) The pH values of the formulations can be between 1 and 14, preferably between 2 and 11 and particularly preferably between 4 and 10.

(62) No limits are set for the concentrations of the effect pigment according to the invention in the formulation. They can bedepending on the applicationbetween 0.001 (rinse-off products, for example shower gels)and 60%. The effect pigment according to the invention can furthermore also be combined with cosmetic active compounds. Suitable active compounds are, for example, insect repellents, inorganic UV filters, such as, for example, TiO.sub.2, UV NBC protection filters (for example OMC, B3, MBC), also in encapsulated form, anti-ageing active compounds, vitamins and derivatives thereof (for example vitamin A, C, E, etc.), self tanners (for example DHA, erytrolose, inter alia) and further cosmetic active compounds, such as, for example, bisabolol, LPO, ectoin, emblica, allantoin, bioflavanoids and derivatives thereof.

(63) Organic UV filters are generally employed in an amount of 0.5-10% by weight, preferably 1-8% by weight, inorganic UV filters in an amount of 0.1-30% by weight, based on the formulation.

(64) The formulations may, in addition, comprise further conventional skin-protecting or skin-care active compounds, such as, for example, aloe vera, avocado oil, coenzyme Q10, green tea extract and also active compound complexes.

(65) The present invention likewise relates to formulations, in particular formulations which, besides the effect pigment according to invention, comprise at least one constituent selected from the group of the absorbents, astringents, antimicrobial substances, antioxidants, antiperspirants, antifoaming agents, antidandruff active compounds, antistatics, binders, biological additives, bleaches, chelating agents, deodorisers, emollients, emulsifiers, emulsion stabilisers, dyes, humectants, film formers, fillers, fragrances, flayours, insect repellents, preservatives, corrosion-protection agents, cosmetic oils, solvents, oxidants, plant constituents, buffer substances, reducing agents, surfactants, propellant gases, opacifiers, UV filters and UV absorbers, denaturing agents, aloe vera, avocado oil, coenzyme Q10, green tea extract, viscosity regulators, perfume, inorganic pigments, such as, for example, transparent or opaque white, coloured and black pigments, metal pigments, temperature-stable ceramic pigments, ceramic colour bodies, functional pigments, such as, for example, IR-reflective pigments or electroconductive pigments, and vitamins.

(66) The invention furthermore relates to the use of the effect pigments according to the invention in paints, coatings, printing inks, security printing inks, plastics, ceramic materials, glasses, glazes, as tracers, as absorbers for the laser marking of plastics and papers and in cosmetic formulations. The pigments according to the invention are furthermore also suitable for the preparation of pigment preparations and for the preparation of dry preparations, such as, for example, granules, chips, pellets, briquettes, etc. The dry preparations are suitable, in particular, for paints and printing inks.

(67) The invention furthermore also relates to formulations, such as, for example, ceramic colours, coatings, tiles, cast ceramics, sanitary ceramics, enamels, glazes, clay, glass and ceramic products, which comprise the effect pigment according to the invention.

(68) The following examples are intended to explain the invention, but without limiting it. Unless indicated otherwise, per cent numbers relate to per cent by weight.

EXAMPLES

Example 1

(69) 100 g of natural mica having a particle size of 10-60 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained is calcined at 850 C. for 0.5 h and sieved.

(70) A temperature-stable golden multilayered pigment having high brightness is obtained.

Example 2

(71) 100 g of natural mica having a particle size of 10-25 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(72) A temperature-stable golden multilayered pigment having high brightness and good hiding power is obtained.

Example 3

(73) 100 g of natural mica having a particle size of 20-180 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 38 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 508 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 431 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. A further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is subsequently carried out. The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment is calcined at 850 C. for 0.5 h and sieved.

(74) A temperature-stable golden multilayered pigment having a strong glitter effect is obtained.

Example 4

(75) 100 g of natural mica having a particle size <15 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 53 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 640 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 501 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and then sieved.

(76) A temperature-stable golden multilayered pigment having high hiding power is obtained.

Example 5

(77) 100 g of Al.sub.2O.sub.3 flakes having a particle size of 5-30 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. A further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is subsequently carried out. The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the Al.sub.2O.sub.3 flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained is calcined at 850 C. for 0.5 h and sieved.

(78) A temperature-stable golden multilayered pigment having a strong glitter effect is obtained.

Example 6

(79) 100 g of borosilcate glass flakes having a particle size of 20-200 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 38 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 508 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 431 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the glass flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment is calcined at 850 C. for 0.5 h and sieved.

(80) A temperature-stable golden multilayered pigment having a very strong glitter effect is obtained.

Example 7

(81) 100 g of SiO.sub.2 flakes having a particle size of 10-40 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. A further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is subsequently carried out. The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the SiO.sub.2 flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment is calcined at 850 C. for 0.5 h and sieved.

(82) A temperature-stable golden multilayered pigment having high brightness and good hiding power is obtained.

Example 8

(83) 100 g of synthetic mica having a particle size of 10-40 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(84) A temperature-stable golden multilayered pigment having high brightness and moderate hiding power is obtained.

Example 9

(85) 100 g of mica having a particle size of 10-60 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 1040 ml of an aqueous solution containing FeCl.sub.3 (w(Fe)=4%) and TiCl.sub.4 (95 g of TiCl.sub.4/l) is added at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 1150 ml of a solution containing FeCl.sub.3 (w(Fe)=4%) and TiCl.sub.4 (95 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the mica substrate coated in this way is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(86) A temperature-stable golden multilayered pigment having high brightness is obtained.

Example 10

(87) 100 g of natural mica having a particle size of 5-40 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(88) A temperature-stable golden multilayered pigment having high brightness and a fine texture is obtained.

Example 11

(89) 100 g of talc having a particle size <10 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the talc flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(90) A temperature-stable golden multilayered pigment having high hiding power is obtained.

Example 12

(91) 100 g of natural mica having a particle size of 10-60 m are heated to 85 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 30 g of FeCl.sub.3 solution (w(Fe)=14%) is metered in at pH 3.1, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(92) A temperature-stable reddish, golden multilayered pigment having high brightness is obtained.

Example 13

(93) 100 g of natural mica flakes having a particle size of 10-60 m are heated to 75 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 50 g of CrCl.sub.3 solution (w(CrCl.sub.3)=19% is metered in at pH 5.9, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. This is then followed by a further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%). The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the coated mica substrate is filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained in this way is calcined at 850 C. for 0.5 h and sieved.

(94) A temperature-stable greenish, golden multilayered pigment having high brightness is obtained.

Example 14

(95) 100 g of Al.sub.2O.sub.3 flakes (doped with TiO.sub.2) having a particle size of 5-30 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. A further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is subsequently carried out. The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the Al.sub.2O.sub.3 flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained is calcined at 850 C. for 0.5 h and sieved.

(96) A temperature-stable golden multilayered pigment having a strong glitter effect is obtained.

Example 15

(97) 100 g of Al.sub.2O.sub.3 flakes (doped with ZrO.sub.2) having a particle size of 5-30 m are heated to 80 C. in 2 l of demineralised water with stirring. When this temperature has been reached, 44 g of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) is metered in at pH 1.8, during which the pH is kept constant using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 by means of sodium hydroxide solution, and 600 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 462 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) are added simultaneously at this pH and 75 C. Throughout the addition time, the pH is kept constant by simultaneous dropwise addition of a 32% sodium hydroxide solution. After stirring for a further 0.5 h, the pH is raised to 7.5, and 650 ml of sodium water-glass solution (13% by weight of SiO.sub.2) are slowly metered in at this pH, during which the pH is kept constant using 10% hydrochloric acid. After stirring for a further 0.5 h, the pH is lowered to pH 1.8 using 10% hydrochloric acid, and a solution of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is metered in. 105 ml of TiCl.sub.4 solution (400 g/l of TiCl.sub.4) are then slowly metered in at the same pH. A further addition of a solution consisting of 5 g of SnCl.sub.45 H.sub.2O and 41 ml of hydrochloric acid (20%) is subsequently carried out. The pH is in each case kept constant at 1.8 using 32% sodium hydroxide solution. The pH is subsequently adjusted to pH 2.8 again by means of sodium hydroxide solution. Finally, the outermost layer is applied by parallel addition of 650 ml of an aqueous FeCl.sub.3 solution (w(Fe)=7%) and 499 ml of an aqueous TiCl.sub.4 solution (200 g of TiCl.sub.4/l) and simultaneous titration with sodium hydroxide solution (w=10%). After stirring for a further 0.5 h at pH 3.0, the Al.sub.2O.sub.3 flakes coated in this way are filtered off, washed and dried at 110 C. for 16 h. Finally, the effect pigment obtained is calcined at 850 C. for 0.5 h and sieved.

(98) A temperature-stable golden multilayered pigment having a strong glitter effect is obtained.

(99) The golden multilayered pigments of Examples 1 to 15 are all stable at temperatures of 1000 C. and exhibit no impairment with respect to the optical properties at these temperatures.