The present invention relates to a method of producing coloured portions on a tyre.
In recent years, demand has arisen in the tyre industry for producing coloured portions on tyres for various purposes, not least of all for aesthetic reasons.
Techniques adopted so far are based on producing rubber mixes dyed with appropriate pigments.
The most commonly used techniques substantially comprise using three layers: a buffer layer on the inner layers of the tyre; a coloured layer made from the dyed mix referred to above; and an outer cover layer, which is removed prior to marketing.
The drawback of this method lies in deterioration of the coloured portion, mainly due to chemical agents migrating from the inner layers of the tyre to the dyed mix. To slow down deterioration, the common practice is to increase the thickness of the coloured layer, which invariably poses problems in terms of heat generation and, therefore, rolling resistance.
It is an object of the present invention to provide a method of producing coloured portions on a tyre, designed to eliminate the drawbacks of the known art.
According to the present invention, there is provided a method of producing coloured portions on a tyre; said method being characterized by comprising the steps of:
The water-based emulsion preferably comprises at least a cross-linkable polymer base, and a surface-active agent of molecular formula (I)
The aliphatic group R1 preferably comprises a double bond.
The surface-active agent preferably has a molecular formula in the group comprising:
The fillers are preferably in the group comprising kaolin, clay, mica, feldspar, silica, graphite, bentonite, and alumina.
The cross-linkable polymer base preferably comprises polymers with a Tg>0° C.
The method according to the present invention preferably comprises a preliminary step of laser carving said part of the tyre to be coloured.
Said water-based paint preferably comprises UV curing photoactivators.
Said coloured portion is preferably heat treated further to improve its mechanical properties.
The following are purely non-limiting examples to give a clearer understanding of the invention.
The following is a description of mixes from which to make the protective layers of the present invention.
These mixes are all characterized by being highly impermeable, as a result of using high-Tg polymers or large amounts of clay.
Use of high-Tg polymers and mineral fillers is made possible by the mixes being made from water-based emulsions comprising at least a surface-active agent of molecular formula (I). Producing mixes using the traditional Banbury mixer method, mixing components such as high-Tg polymers or mineral fillers would take too much power, and so be unviable both ecologically and economically. Being mixed in emulsion, the mixes according to the present invention, on the other hand, all require the same amount of energy, regardless of the components used.
The protective layers are therefore made from the resulting mixes, by depositing a water-based emulsion on a tyre part for colouring, e.g. the sidewall, and then evaporating the water.
The water-based emulsions are each produced by dispersing and mixing the various mix components in water, and more specifically by dispersing all the components in Table I simultaneously in 1 L of water. The resulting aqueous dispersion is stirred mechanically for 30 minutes and then sonicated for 15 minutes to obtain a water-based emulsion.
The above method of producing the water-based emulsions in no way constitutes a limitation of the method according to the present invention.
The emulsion is sprayed or brushed onto the sidewall of the tyre, and, once applied, the water in the emulsion is evaporated to typically form a roughly 0.3 mm thick protective layer, to which a water-based paint is applied. More specifically, a water-based paint in the group known as “VERNICI IMC IDRO” or “IMC IDROFLEX”, produced and marketed by SIVAM VERNICI SPA, is used.
The protective layer and the water-based paint layer may be cross-linked simultaneously with or after curing the tyre. In other words, the painting method may be applied to a cured or green tyre.
Colourfastness was tested to assess the advantages of the invention with respect to the known art.
A fade index AE was used, as established at the 1976 International Commission on Illumination, and defined by the formula:
The difference in colour was determined by comparing the colour on the day the coloured portion was produced, with the colour thirty days later. The 100 ΔE value corresponds to a complete absence of fading.
Adhesion of the protective layer to the sidewall of the tyre was determined as per ASTM Standard D624.
In the following examples, two different surface-active agents (a, b) in the molecular formula (I) class were used:
Table I shows the compositions in phr of five mixes A-E made from respective emulsions in accordance with the present invention, and, for each composition, the relative fade value ΔE and relative adhesion to the tyre sidewall. In mixes A-E, the composition of the polymer base was varied by inserting increasingly high Tg polymers.
As shown clearly in Table I, the method according to the present invention provides for highly effective colouring in terms of fastness, as well as satisfactory adhesion of the protective layer to the coloured tyre portion.
Table II shows the compositions in phr of three mixes F-H made from respective emulsions in accordance with the present invention, and, for each composition, the relative fade value AE and relative adhesion to the tyre sidewall. In mixes F-H, clay was inserted in gradually increasing amounts.
Table II also shows clearly how the method according to the present invention provides for highly effective colouring in terms of fastness and also adhesion to the tyre.
The fillers used in the protective layer according to the present invention preferably comprise mineral particles of 0.2 to 2 μm diameter, and an aspect ratio of 5 to 30 and preferably 8 to 20, and are preferably in the group comprising kaolin, clay, mica, feldspar, silica, graphite, bentonite and alumina.
An important point to note is the much lower cost of the method according to the present invention, as compared with known methods. In fact, producing a mix from a water-based emulsion, as opposed to mixing in a Banbury mixer, enables considerable energy saving, as well as optimum dispersion of the emulsion components, regardless of type.
The method according to the present invention also provides for colouring a tyre, adding only very thin layers of material, with practically no effect on rolling resistance. In fact, the protective layer, being made from a water-based emulsion and a highly impermeable mix, may be made very thin, of a thickness ranging from 0.001 to 0.5 mm.
As stated, the method according to the present invention applies to both cured and green tyres.
When colouring a cured tyre, in a preferred embodiment of the present invention, the tyre part for colouring is first carved with a laser, e.g. a CO2 laser, to form a groove pattern, over which the protective layer and paint layer are applied to grip them mechanically to the tyre and so ensure firmer grip of the paint layer to the tyre. In fact, in addition to chemical adhesion of the protective layer to the tyre surface, mechanical grip by the groove pattern also assists in securing the paint layer to the tyre. The groove pattern also reduces mechanical stress, to prolong the working life of the paint layer.
In another preferred embodiment of the present invention, when colouring a cured tyre, the water-based paint comprises UV curing photoinitiators for fast- curing the paint locally by appropriate UV illumination, without subjecting the cured tyre to additional thermal stress.
Finally, the method according to the present invention preferably comprises a finishing step, in which the coloured part is laser processed to produce an attractive geometric effect on the paint layer, and so reduce the visual effects of in-service fading of the rubber.
Number | Date | Country | Kind |
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TO2009A000964 | Dec 2009 | IT | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IB2010/003166 | 12/9/2010 | WO | 00 | 8/13/2012 |