GB2487879A

GB2487879A - Colouring tin

Info

Publication number: GB2487879A
Application number: GB1208941.3A
Authority: GB
Inventors: Trish Woods
Original assignee: Plymouth University
Current assignee: Plymouth University
Priority date: 2008-10-22
Filing date: 2008-10-22
Publication date: 2012-08-08
Anticipated expiration: 2028-10-22
Also published as: GB201208941D0; GB2487879B

Abstract

A method of colouring the surface of a tin-containing article, wherein the method comprises contacting the surface of the article with a solution comprising a thiosulphate, preferably under neutral or acidic conditions. The thiosulphate is typically a sodium or potassium thiosulphate aqueous solution. A weak acid is preferably provided such as acetic acid and the solution may further comprise an aldehyde/ketone, polyol and /or a copper salt. In one embodiment, the solution contains sodium thiosulphate and citric acid and further comprises a copper salt, together with acetone and/or glycerol. The method is preferably conducted at elevated temperatures, in particular by heating the solution to a temperature of 45Â°C to 85Â°C. The tin article may be pewter or another alloy of tin. A method of identifying an elevation in temperature in a tin article, comprises monitoring the colour of the surface of a tin article, wherein at least a portion of the surface has been treated at ambient temperature by the above method.

Description

A METHOD OF COLOURING TIN AND TIN-CONTAINING ARTICLES

The present invention relates to a method for colouring the surface of tin and tin-containing articles, such as articles of pewter and other alloys of tin.

The colouring of metals is well known, with techniques for the colouring of such metals as copper having been well known for many years. However, comparatively little is known regarding the colouring of tin and tin-containing alloys.

In part this is due to the generally high level of inertness exhibited by tin.

Pewter is an alloy of tin, containing from 85 to 99% by weight of tin and from 1 to 15% by weight of copper to provide the alloy with a degree of hardness.

Traditionally, lower grades of pewter have contained lead. However, modern trends are to replace the lead with antimony or bismuth. It is known to colour the surface of pewter articles, in particular to darken the article to replicate the dark grey patina of old lead pewter. Specific techniques for darkening the surface of pewter articles are disclosed in Publication No. 566 Working with pewter', published by the International US patent No. 3,930,898 discloses a process for imparting a dark patina to the surface of an article formed from a low melting metal alloy, including alloys of tin such as pewter. The method comprises exposing the surface of the article to an acid solution of a copper salt, in particular copper sulphate, copper chloride or copper nitrate.

US patent No. 6,013,328 concerns a electroless method of antiquing a pewter component, the method comprising contacting the component with an oxidizing solution containing copper chloride, selenious acid, hydrochloric acid and sodium tetradecyl sulphate.

Other techniques for colouring tin and pewter are referred to in the art.

Harris, C. Colouring Miscellaneous Metals: silver-tin-gold-zinc-cadmium-nickel', Metal Industry, January 1951, pages 71 to 73, describes various electrolytic colouring

I

processes for tin and pewter, similar to those applied to aluminium. Further, various lacquering techniques have been practiced for a number of centuries.

While certain techniques for colouring tin are known, the practice of colouring tin-containing articles is by no means as well developed as with many other metals.

As a result, there is a need for a simple method for colouring tin and tin-containing articles, such as pewter articles. It would be an advantage if the method could be applied with only simple modifications to provide a range of different colourations on the surface of the article.

According to a first aspect of the present invention there is provided a method for colouring the surface of a tin-containing article, the method comprising contacting the surface of the article with a solution of a thiosulphate salt.

It has been found that a solution of a thiosulphate salt causes the surface of the tin article to change colour, in particular to take on a gold colour. The intensity and particular hue of the colour will depend upon the specific conditions under which the surface is treated, as will be described hereinafter. As a result, the method of the present invention allows a tin-containing article to have its surface treated to give it a wide range of colourations. It has further been found that the colouration of the surface is sufficiently stable and resistant to form a permanent colouration of the article.

The method of the present invention may be applied to a wide range of tin-containing materials. The material may consist substantially entirely of tin.

Alternatively, the material may be an alloy of tin. In this case, the material should contain tin as the major component, in particular greater than 50% by weight, preferably more than 60%, more preferably more than 75% by weight, especially more than 80%. The method of the invention is particularly suitable for application to pewter articles. The method may be applied to the entire range of pewters, that is alloys of tin and copper containing from 85 to 99% by weight of tin, optionally with the inclusion of lead, antimony and/or bismuth.

The method employs a solution of a thiosulphate salt. The solution is most preferably an aqueous solution.

The thiosulphate salt may be any suitable thiosulphate salt. It has been found that thiosuiphates of monovalent cations are particularly suitable. Preferred salts are thiosuiphates of alkali metals, in particular potassium and sodium. Ammonium thiosuphate is a further preferred thiosulphate salt for use in the method of the present invention.

The solution may contain the thiosuiphate in any suitable amount. Preferably, the thiosulphate is present in the solution at a concentration in the range of from 5 to 50g per 100 ml, more preferably from 10 to 40g per 100 ml, especially from 20 to 30g per 100 ml of solution. A concentration of about 25g per lOOmI of solution is particularly suitable.

The thiosulphate solution may be contacted with the surface of the tin article under a range of pH conditions. Preferably, the solution is not strongly alkali, that is having a pH substantially higher than 7. Rather, it is preferred that the tin is contacted with the thiosulphate solution under substantially neutral or acidic conditions, that is a pH below 7. In one embodiment, it is preferred that the conditions are mildly acidic, with the preferred pH range being from 5 to 6, more preferably from 5 to 5.5. It has been found that the colouration of the tin article can depend upon the pH of the thiosulphate solution. In particular, to achieve gold colouration, the pH value is preferably in the range of from 5 to 5.5. The addition of components, such as copper sulphate, to achieve blue and green colours generally increases the pH to around 7.

The acidic conditions may be obtained by the presence of any suitable acidic compound or compounds in the solution. It is preferred that the acidic conditions are obtained by the presence of a weak acid. In this respect, a weak acid is an acid having a Ka value of from about 1 O to 1 0b0. Suitable weak acids include organic acids, with acetic acid and citric acid being particularly preferred.

The method of the present invention may be performed with a solution consisting of a thiosulphate salt, a suitable solvent and a component to provide the required acidity. However, it has been found that the addition of one or more components can provide the colouration of the surface with increased stability, in particular when using an aqueous thiosulphate solution. Such stabilizers include organic solvents, in particular aldehydes and ketones, especially ketones. Lower organic solvents are preferred, that is compounds having from 3 to 8 carbon atoms.

A particular preferred stabilizer is acetone or butanone. It has been found that the inclusion of acetone in an aqueous thiosulphate solution imparts a significant stability to the colouration. It has been observed that the acetone acts as a wetting agent for the surface being treated, ensuring that the thiosulphate solution contacts the surface.

Aldehydes and ketones may be present in the thiosulphate solution in any suitable amount. Preferably, the aldehydes and ketones are present in an amount in the range of from 0.5 to 10 ml per 100 ml of solution, more preferably from 1 to 5 ml, especially from 1.5 to 2.5 ml per 100 ml of solution.

Alternatively, or in addition, to the aforementioned stabilizers, the thiosulphate solution may contain one or more alcohols, in particular a polyol. Lower alcohols are preferred, that is compounds having from 3 to 8 carbon atoms. A particularly preferred polyol is glycerol. It has been found that the inclusion of a polyol, such as glycerol the layer of colouration on the surface of the tin article is generally of greater thickness. It has been observed that a thicker layer of colouration can provide the surface with a wider range of effects, in particular arising from light interference patterns.

One or more polyols may be present in the thiosulphate solution in a suitable amount. Preferably, if employed, the polyol is present in an amount in the range of from 0.1 to 2 ml per 100 ml of solution, more preferably from 0.5 to 1.5 ml, especially from 0.75 to 1.25 ml per 100 ml of solution. A particularly suitable concentration for the polyol is about 1 ml per 100 ml of solution.

As noted above, the use of a thiosulphate solution, optionally with an aldehyde or ketone, and/or a polyol, results in the surface of the tin article taking on a colour with a gold hue. Other colours may be obtained by the addition of further components to the thiosuphate solution. In particular, the addition of one or more copper salts results in the surface having one or a mixture of pink, blue and green colouration. Suitable copper salts include copper sulphate and copper acetate.

One or more copper salts may be present in the thiosulphate solution in a suitable amount. If present, the copper salts are present an amount in the range of from ito 15g per 100 ml of solution, more preferably 2 to lOg per 100 ml, especially 3 to 8g per 100 ml. Concentrations of copper salt in the range of from 3 to 6g per ml of solution are particularly preferred.

The thiosulphate solution is preferably contacted with the surface of the tin article at an elevated temperature. It has been found that the method of the present invention provides a colouration of the surface that develops only very slowly, if at all, at temperatures of ambient or below. Elevated temperatures have been found to be necessary to allow the surface to develop a colouration in an acceptable period of time. Elevated temperatures are most suitably applied by heating the thiosulphate solution. Preferred temperatures for conducting the method are at least 30°C, more preferably at least 40 °C. It is preferred that the temperature is below 1 00°C, more preferably below 90°C. In any event, the temperature should not exceed the boiling point of the solvent.

A preferred temperature is in the range of from 45 to 85 °C, more preferably from 55 to 70°C.

The thiosulphate solution is most preferably contacted with the surface of the tin article while being agitated. For example, the agitation may be achieved by the motion of the tin article being immersed in the solution and removed. Other forms of agitation may also be applied, if required. Suitable agitation techniques will be known to the person skilled in the art.

It has been found that the form of the colouration of the surface of the tin article will change over time while the thiosulphate solution is in contact with the surface, depending upon the prevailing conditions, such as acidity, salt content and temperature. In general, the colouration of the surface of the tin develops according to the following schedule: GOLD to PINK to BLUE to GREEN A particular colouration may be obtained by conducting the method until the desired colour or combination of colours has been obtained and then removing the solution from contact with the surface. If further colouration is required, the surface may be further contacted with the thiosulphate solution to move the colouration further along the progression set out above.

The time for contacting the thiosulphate solution with the tin surface will vary according to the colouration to be obtained, the components of the solution and the temperature. In general contact times in the range of from 1 to 20 minutes, more preferably from ito 10 minutes. Very good results have been obtained with contact times of from 2 to 4 minutes. Shorter or longer contact times may be required, depending upon the conditions applied and the result to be achieved. In particular, lower temperatures will require a longer contact time in order to achieve a particular colouration.

Once the desired colouration has been obtained, it is preferred to quench the colouration reactions by washing the surface of the tin article with a cold solvent, most suitably water. In this way, the desired colouration of the surface can be fixed.

The hardness of the surface colouration may be determined using any standard test. One preferred technique uses a range of pencils of different hardness, as described in the examples hereinafter. It has been found that the colouration of the surface can be prepared with a hardness of at least an HB pencil. This is generally recognized as being a stable and resistant surface.

The surface of the tin article may have a suitable coating applied after treatment with the thiosulphate solution, in order to enhance and protect the colouration. Suitable coatings include varnish, in particular acrylic varnishes, and wax.

The surface of the tin article should preferably be cleaned prior to contact with the thiosuphate solution, in particular with a degreasing agent. Suitable cleaning and degreasing agents are well known in the art and commercially available. The surface of the tin article may be smooth, for example a polished surface. Alternatively, the surface may be rough or contoured, for example as may result from sand blasting and the like.

As noted above, it has been found that the colouration of the surface of the tin article is dependent upon the colouring composition being heated. In particular, at low or ambient temperatures no significant colouration arises. It has been found that this effect may be used, by employing a tin-containing article or component treated as hereinbefore described, to detect the presence of an elevated temperature of the article. In particular, once treated, such articles have been found to indicate an increase in temperature by displaying a change of colour.

Accordingly, in a further aspect, the present invention provides a method of identifying an elevation in temperature in a tin article, the method comprising monitoring the colour of the surface of the tin article, at least a portion of the surface being monitored having been treated at ambient temperature according to a method as hereinbefore described.

An indication of the elevated temperature achieved may be obtained from an analysis of the particular colouration of the surface of the article.

Embodiments of the present invention will now be described by way of the following examples, presented here for illustrative purposes only. Images of the treated samples are set out in the accompanying Figures 1 to 6, details of which are described in the examples.

EXAMPLES

Example 1

A treatment solution was prepared as follows: Ammonium thiosulphate (50g) was dissolved in distilled water (200 ml) with stirring. Butanone (5 ml) was added and the resulting mixture further agitated. Citric acid was added, again with stirring, until a pH of 5 was achieved. The resulting solution was heated to between 60 to 802C.

A sample of pewter was coloured using the solution prepared above, as follows: The pewter sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the pewter took up a pale gold colour after immersion in the solution for ito 2 minutes. After immersion in the solution for 5 to 10 minutes, the surface colour of the pewter sample was a bright gold.

The pewter sample was removed from the solution and rinsed in clean, cold water. To prevent the formation of water marks, the sample was rapidly dried using a stream of hot air.

The hardness of the surface colouration was measured as follows: A series of pencils having pencil lead of increasing hardness ranging from 4B to 4H were used to draw lines on the coloured surface. The pencils were used in order of increasing hardness starting with the softest (4B). It was found that the surface colouration started to be removed by the pencil of hardness HB.

The surface of the pewter sample was sealed using a wax.

The treated sample of pewter is shown in Figure 1. The surface of the sample was a bright gold colour.

Example 2

A treatment solution was prepared as follows: Sodium thiosulphate (50g) was dissolved in distilled water (200 ml) with stirring. Copper acetate (12g) was added with stirring. Acetone (5 ml) was added and the resulting mixture further agitated. The resulting solution was heated to 602C.

A sample of pewter was coloured using the solution prepared above, as follows: The pewter sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the pewter took on a progression of colours ranging through pale gold, pink, blue and green. The first phase of colour development occurred rapidly, with the later colours in the progression developing more slowly but brighter. Colour development tended to slow at the gold stage. Some blue colour became evident if the sample was left in contact with the solution a little longer. The final colour of the sample was a green/gold colouration.

The surface of the pewter sample was sealed using a clear acrylic lacquer.

The treated sample of pewter is shown in Figure 2. The surface of the sample was a gold colour with green hues.

Example 3

A treatment solution was prepared as follows: Ammonium thiosulphate (50g) was dissolved in distilled water (200 ml) with stirring. Copper acetate (12g) was added with stirring. Acetone (5m1) was added, again with stirring. The resulting solution was heated to between 50 and 60°C.

A sample of pewter was coloured using the solution prepared above, as follows: The pewter sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the pewter took on a cycle of colour changes from gold to pink to purple to blue then fading to pale green gold. The colour change was rapid with a brighter second colour cycle ocurring. The blue / purple colouration appears the most even. The sample was removed at the desired stage of colour development and rinsed in cold water. The sample was rapidly dried in a stream of air then sealed with a clear acrylic varnish.

The treated sample of pewter is shown in Figure 3. The surface of the sample was a blue/purple colour.

Example 4

A treatment solution was prepared as follows: Ammonium thiosulphate (50g) was dissolved in distilled water (200 ml) with stirring. Copper acetate (12g) was added with stirring. Acetic Acid (3gms) was added with stirring. Acetone (5m1) was added, again with stirring. The resulting solution was heated to between 50 and 60°C.

A sample of pewter was coloured using the solution prepared above, as follows: The pewter sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the pewter took on a cycle of variegated colour changes from gold to pink to purple to blue then fading to pale green gold. The colour change was rapid with a second colour cycle occurring. A variegated pink and blue was obtained. The sample was removed at the desired stage of colour development and rinsed in cold water. The sample was rapidly dried in a stream of air and then sealed with a clear acrylic varnish.

The treated sample of pewter is shown in Figure 4. The surface of the sample was a variegated blue and pink colour.

Example 5

A treatment solution was prepared as follows: Sodium thiosulphate (50g) was dissolved in distilled water (200 ml) with stirring. Copper acetate (log) was added with stirring. Acetone (3m1) was added with stirring. The pH value was measured at 7.2. The resulting solution was heated to between 50 and 60°C.

A sample of tin was coloured using the solution prepared above, as follows: The tin sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the tin took on a cycle of rapid colour changes from gold to pink to green occurred within 2 minutes, then continued to repeat. It was further found that, if the sample was left in the solution the colour changed until reaching a dull gray.

The sample was removed at the desire stage, rinsed in cold water, dried rapidly in a stream of air and then sealed with a clear acrylic varnish.

The treated sample of tin is shown in Figure 5. The surface of the sample in Figure 5 displayed the range of colours from gold to pink to green.

Example 6

A treatment solution was prepared as follows: Ammonium thiosulphate (SOg) was dissolved in distilled water (200 ml) with stirring. Copper acetate (5g) was added with stirring. Butanone (5m1) was added with stirring. The pH value was measured at 7. The resulting solution was heated to between 60 and 80°C.

A sample of tin was coloured using the solution prepared above, as follows: The tin sample was immersed in the solution with gentle agitation. The sample was periodically removed to observe the change in colour. It was found that the surface of the tin underwent a series of rapid colour changes from gold to pink to blue to green, occurring within 30 seconds. If allowed to continue, it was found the colour cycle continues to repeat until reaching a dull gray. The sample was removed at the desired stage in the colour cycle, rinsed in cold water, dried rapidly in a stream of air then sealed with a clear acrylic varnish.

The treated sample of tin is shown in Figure 6. The surface of the sample in Figure 5 displayed the range of colours from gold to pink to blue to green.

Claims

CLAIMS1. A method of colouring the surface of a tin-containing article, the method comprising contacting at least a portion of the surface of the article with a solution comprising a thiosulphate.
2. The method according to claim 1, wherein the tin article comprises at least 50% byweighttin.
3. The method according to claim 2, wherein the tin article comprises at least 75% by weight tin.
4. The method according to any preceding claim, wherein the tin article comprises an alloy of tin.
5. The method according to any preceding claim, wherein the tin article is of pewter.
6. The method according to any preceding claim, wherein the solution is an aqueous solution.
7. The method according to any preceding claim, wherein the thiosulphate is a salt of a monovalent cation.
8. The method according to claim 7, wherein the monovalent cation is an alkali metal or ammonium.
9. The method according to claim 8, wherein the monovalent cation is sodium or potassium.
10. The method according to any preceding claim, wherein the thiosulphate is present in the solution in an amount in the range of from 5 to 50g per 100 ml.
11. The method according to any preceding claim, wherein the solution is substantially neutral or acidic.
12. The method according to claim 11, wherein the solution has a pH of from 5 to 6.
13. The method according to claim 12, wherein the solution has a pH of from 5 to 5.5.
14. The method according to any of claims 11 to 13, wherein the acidic conditions are provided by the presence of a weak acid in the solution.
15. The method according to claim 14, wherein the weak acid is acetic acid or citric acid.
16. The method according to any preceding claim, wherein the solution comprises an aldehyde or a ketone.
17. The method according to claim 16, wherein the solution comprises acetone.
18. The method according to either of claims 16 or 17, wherein the aldehyde or the ketone is present in an amount of from 0.5 to 10 ml per 100 ml of solution.
19. The method according to any preceding claim, wherein the solution comprises apolyol.
20. The method according to claim 18, wherein the solution comprises glycerol.
21. The method according to either of claims 19 or 20, wherein the polyol is present in an amount of from 0.1 to 2 ml per 100 ml of solution.
22. The method according to any preceding claim, wherein the solution comprises a copper salt.
23. The method according to claim 22, wherein the copper salt is copper sulphate or copper acetate.
24. The method according to either of claims 22 or 23, wherein the copper salt is present in an amount of from ito 15g per 100 ml of solution.
25. The method according to any preceding claim, wherein the article is contacted with the solution at an elevated temperature.
26. The method according to claim 25, wherein the solution is heated to a temperature of at least 30°C.
27. The method according to claim 26, wherein the solution is heated to a temperature of from 45 to 85°C.
28. The method according to any preceding claim, wherein the solution is agitated while being contacted with the surface of the article.
29. The method according to any preceding claim, wherein the solution is contacted with the article for a period of from 1 to 20 minutes.
30. The method according to any preceding claim, further comprising quenching the surface of the article once contact with the solution has ceased.
31. The method according to claim 30, wherein the surface is quenched using cold water.
32. The method according to any preceding claim, wherein at least the portion of the surface of the article to be contacted with the solution is cleaned prior to contact with the solution.
33. A coloured tin article prepared by a method according to any preceding claim.
34. A method of identifying an elevation in temperature in a tin article, the method comprising monitoring the colour of the surface of the tin article, at least a portion of the surface being monitored having been treated at ambient temperature according to a method as claimed in any of claims 1 to 25 or claims 28 to 32.
35. A method substantially as hereinbefore described.
36. A coloured tin article substantially as hereinbef ore described.