PHOSPHORESCENT TIMEPIECE COMPONENT

Abstract

A timepiece component including a phosphorescent multilayer structure (3) comprising a front layer (1) with a transparent or translucent polymer matrix and comprising phosphorescent pigments and a reflective underlying layer (2).

Claims

1. A timepiece component comprising a phosphorescent multilayer structure (3) comprising a front layer (1) with a transparent or translucent polymer matrix and comprising phosphorescent pigments and a reflective underlying layer (2).

2. The timepiece component according to claim 1 wherein the front layer (1) comprises an elastomer matrix.

3. The timepiece component according to claim 1, wherein the underlying layer (2) comprises a polymer matrix charged with a reflective pigment.

4. The timepiece component according to claim 3 wherein the reflective pigment comprises titanium oxide.

5. The timepiece component according to claim 3, wherein the polymer matrix of the underlying layer (2) is compatible with the polymer matrix of the front layer (1).

6. The timepiece component according to claim 5, wherein the front layer (1) and the underlying layer (2) comprise a fluoroelastomer.

7. The timepiece component according to claim 1, wherein the front layer (1) has a thickness comprised between 0.03 mm and 1 mm.

8. The timepiece component according claim 1 forming a watch bracelet (4), a watch dial, hands, a bezel or a watch case.

Description

BRIEF DESCRIPTION OF THE FIGURES

[0016] FIG. 1 is a schematic sectional view illustrating the phosphorescent multilayer structure of a timepiece component according to the invention.

[0017] FIG. 2 shows a schematic view of a watch comprising a bracelet forming a horological component according to the invention.

REFERENCES OF THE FIGURES

[0018] 1. Phosphorescent layer [0019] 2. Reflective layer [0020] 3. Watch bracelet [0021] 4. Watch

DETAILED DESCRIPTION

[0022] The present invention relates to a timepiece component comprising a phosphorescent multilayer structure allowing to maximise the luminous performances of the structure while minimising the amount of phosphorescent pigments in the complete structure. This structure is particularly adapted for the manufacture of a timepiece component intended to produce watch bracelets. It goes without saying that the horological component can also form other constituent elements of a wristwatch such as a watch dial, hands or else a bezel or a watch case.

[0023] According to the invention, the multilayer structure comprises a front face, intended to be seen in normal use, and a rear face intended, for example, to be in contact with the skin in the case of a watch bracelet.

[0024] According to the invention, the front face comprises a transparent or translucent polymeric front layer 1 comprising a phosphorescent pigment. The thickness of this layer is optimised so that the light emitted by the deepest pigments is not excessively absorbed by the material comprised between said deep pigment and the surface. Depending on the optical features of the polymer matrix of the layer, this layer has a thickness comprised between 30 μm and 1 mm.

[0025] A thin transparent layer can optionally be added on top of the phosphorescent layer, as long as it does not significantly absorb the emitted light. Such an additional layer can for example be added to improve the surface finish of the final product or to protect the area comprising the pigment.

[0026] A reflective layer 2 is disposed under the front layer. This layer can either be a thin reflective layer such as a thin metal layer deposited for example by evaporation or plasma deposition on a substrate, or, preferably, a layer of polymer charged with a reflective pigment such as, for example, titanium oxide. This layer can also be deposited on a substrate or even be a self-supporting layer. This layer 2 can for example form the rear layer 2 of the bracelet in contact with the skin as shown in FIGS. 1 and 2. However, the structure could comprise a third layer (not shown) which is for example coloured, for example disposed the on top of the front layer 1, the important thing to solve the aforementioned problem being that the layer immediately under the phosphorescent layer is reflective.

[0027] The small size of the TiO.sub.2 particles (typically comprised between 200 nm and 400 nm) maximises the reflection of visible light. The base mixture advantageously comprises an elastomer, a vulcanisation system, silica, titanium oxide and an optical brightener.

[0028] In order to have sufficient reflection, the reflecting layer, when it is polymeric in nature as described above, has a thickness of at least 20 μm, preferably at least 40 μm.

[0029] The front layer 1 and the reflective layer, when it is of polymeric nature, are preferably selected from the group comprising a fluorinated elastomer of the FKM family or a thermoplastic elastomeric polymer of the TPU (Polyurethanes), EVA (Ethylene vinyl acetate copolymer), silicone, EPR (ethylene propylene rubber) family and their thermoplastic derivatives (TPO) or else from the family of acrylic elastomers, or a mixture of the latter.

[0030] In the case of a watch bracelet, the total thickness of the rear layer, under the phosphorescent layer, therefore comprising the reflective layer 2 and an optional additional layer, has a thickness comprised between 20 μm and 1.5 mm.

[0031] Three shaping techniques are preferred for making bracelets: [0032] The lower layer can be moulded onto the upper phosphorescent elastomer layer (or vice versa) [0033] The phosphorescent layer can be produced by moulding and the reflective layer can be coated by spraying. [0034] The two layers (produced separately by injection or compression) can be assembled using the “saddle bracelet” type shaping technique: the two layers are glued and sewn together to form a bracelet.

Exemplary Embodiment

[0035] A. Preparation of the Substrate.

[0036] A fluoroelastomer is prepared by mixing a pure FKM Tecnoflon® P-457 grade from Slovay by working on an open mixer with 5% titanium oxide.

[0037] At the end of the mixing, a vulcanisation system is added (2.5% by weight of Luperox® 101XL-45+3% by weight of Drimix® TAIC 75%, the percentages being expressed relative to the polymer).

[0038] Preferably, Nafol 1822B™ oil marketed by Sasol (up to 1.8%) is also added. The whole constitutes the ready-to-shape reflective FKM mixture.

[0039] This mixture is shaped by compression and partially crosslinked.

[0040] B. Preparation of the phosphorescent layer

[0041] The following masterbatch is produced:

[0042] Pure FKM Tecnoflon® P-457 grade by Solvay which is produced on a clean line and which is transparent is used as the masterbatch matrix.

[0043] Tecnoflon® P-457 is diluted in a 1:1 ratio in methyl ethyl ketone (Methyl Ether Ketone or MEK).

[0044] A photoluminescent pigment previously sieved at 30 μm is incorporated into the mixture obtained in the previous step, the amount of pigment being in a ratio 1:1 with respect to Tecnoflon® P-457 and the whole is mixed in a high speed mixer at 3000 rpm.

[0045] A fluorochrome is introduced in an amount of 0.5% relative to the total (that is to say 1.5% relative to the FKM polymer) and the whole is again mixed in a high speed mixer at 3000 rpm.

[0046] The solvent is evaporated in an oven at 80° C. until the solvent is removed.

[0047] The masterbatch produced beforehand is incorporated up to a minimum of 60% in a pure FKM P-457 by working on an open mixer.

[0048] At the end of the mixing, a vulcanisation system is added (2.5% by weight of Luperox® 101XL-45+3% by weight of Drimix® TAIC 75%, the percentages being expressed relative to the polymer).

[0049] Preferably, Nafol 1822B™ oil marketed by Sasol (up to 1.8%) is also added. The whole constitutes the optimised photoluminescent FKM mixture, ready to be shaped and crosslinked.

[0050] The mixture B obtained is then overmoulded by compression and crosslinked on the substrate A prepared beforehand.

[0051] The component thus obtained comprises a front layer of 100 μm having a pigment concentration of 30% adherent to a reflective elastomer layer comprising 10% of titanium oxide.