EP0083571A1

EP0083571A1 - Method of reducing corrosion of aluminium components

Info

Publication number: EP0083571A1
Application number: EP83300018A
Authority: EP
Inventors: Ronald William Elkington; David Francis Fletcher; Albert Harold Carter
Original assignee: Alcan International Ltd Canada
Current assignee: Rio Tinto Alcan International Ltd
Priority date: 1982-01-06
Filing date: 1983-01-05
Publication date: 1983-07-13
Also published as: EP0083571B1; GB8300120D0; GB2114113B; DE3362966D1; GB2114113A

Abstract

The corrosion of aluminium components in contact with circulating water, e.g. in radiators of heating systems, is reduced by providing a surface film of finely divided magnetite (Fe₃0₄). This may be achieved by introducing colloidal magnetite into the circulating water, preferably in conjunction with a surface active agent and a supplementary inhibitor to reduce galvanic corrosion in the presence of copper or brass.

Description

The present invention relates to the inhibition of corrosion in circulating water systems which include aluminium or aluminium alloy components; it is particularly advantageous when used in the operation of heating systems employing hot water radiators made of aluminium alloys.
Aluminium and its alloys have a number of attractions as materials for the construction of hot water radiators, for example their light weight and good heat emissivity characteristics. Such radiators may be manufactured in various ways, for example by casting methods, by fabrication from sheet or plate, or by assembly of suitable extruded sections. When the radiators are produced by casting, the alloy used is generally an aluminium-silicon alloy, for example Al-11% Si. For other methods, commercially pure aluminium (99.5%) can be used but its mechanical strengths and other properties are generally inadequate and alloys of aluminium are preferred. In the case of radiators fabricated from extruded sections, alloys of the aluminium-magnesium silicide group such as AA 6063 are much preferred.
It has, however, been found that aluminium and its alloys may undergo pitting corrosion when in contact with potable water drawn from domestic supplies and subjected to the temperature cycles normally encountered in radiators; in particular such pitting corrosion is liable to occur when the system includes copper-containing components so as to provide a source of copper ions in the water.
It is an cbject of the invention to provide a means of decreasing or avoiding the onset of such pitting attack, which seems to be dependent upon combinations of conditions of electrolyte content and aeration of the water and possibly upon other factors, which are not at present fully understood.
British Patent Specification 2013168A describes a method of inhibiting corrosion of a body of e.g. aluminium in the presence of water by adding to the water ferrous sulphate and an organic polymer, preferably in the presence of a reducing or chelating agent, so as to dep-osit an even layer of ferric hydroxide on the body.
All aluminium surfaces, which are maintained in contact with hot water under conditions of aeration, develop a Bayerite-type hydrated oxide coating. It was observed that when pieces of an aluminium-11% silicon alloy from a cast radiator were subjected to water circulating in a central heating system under experimental conditions, slight pitting corrosion occurred initially; however on prolonged contact with the water, a dark coloured film developed on the surface of the metal and the pitting corrosion did not progress any further as would have been expected in the normal course of such corrosion. Indeed it became clear that the surface of the aluminium alloy had become protected against further pitting attack and that this protection was associated with the dark-coloured film.
It was at first assumed that the stifling of pitting corrosion and the dark colours of the film were caused by the incorporation into the film of silicon or a silicon compound derived from the Al-Si alloy. However,, further study of the film revealed surprisingly that the dark colour and the protective properties were not caused by silicon but were in fact due to the presence of very finely divided magnetite, Fe₃O₄, integral with the Bayerite layer. It has also been found that such protective films could be formed on aluminium surfaces in general and were not confined to high silicon alloys of the type involved in the initial experiment. Such films can, for example, be developed on the internal surfaces of radiators assembled from extruded sections made in alloy AA 6063 and other common extrusion alloys.
The magentite particles were of a size less than 0.1 µm, i.e.of colloidal dimensions and presumably originated from some colloidal solution and originated with some chance source of iron in contact with the water.
Some domestic hot water radiator systems to-day are free of iron components. In other such systems chance sources of iron, such as the water heating jacket of the boiler, exist, but may not give rise to colloidal particles of magnetite incorporated into the Bayerite film under the operating conditions.
According to the present invention, there is provided a method of reducing corrosion of the surface of an aluminium or aluminium alloy component in contact with circulating water, which method comprises providing on the surface a protective oxide layer containing finely divided particles of magnetite.
Preferably, a source of colloidal magnetite is introduced into the circulating water so as to form on the surface of the component the protective film of magnetite. Thus colloidal magnetite may be introduced into the circulating water, preferably at a concentration of from 500 ppm to 10000 ppm. Below 500 ppm, the protective film may be developed only slowly or to an insufficient extent. Amounts above 10000 ppm contaminate the circulating water without providing sufficient compensating advantages.
The method of the invention may be used to pretreat the component before it comes in contact with the circulating water. Preferably, however, the source of colloidal magnetite is introduced into the circulating water at substantially the same time as the component, whereby there is formed on the surface thereof a protective layer of hydrated alumina containing the finely divided particles of magnetite.
The most convenient route for applying the treatment to an aluminium radiator in situ in a heating system is to dose the water in the radiator system with a magnetite-bearing material in colloidal form or in at least such a fine state of suspension that it can only remain in a settled out condition when entrapped in the growing layer of Bayerite on the surface of aluminium in contact with the water.
In one test magnetite of an average particle size of about 0.2 µm was dispersed in water at a temperature of 70 to 75⁰C and circulated through an aluminium alloy pipe in the presence of a copper gauze. It was found that such magnetite was quickly absorbed into the Bayerite layer on the internal surface of the pipe. It was found that the dark-coloured Bayerite layer was highly protective and after a test under these conditions over a three month period the aluminium surface was found to be essentially free from pitting.
Preferably, a surface active agent is also introduced into the circulating water in order to assist dispersion of the colloidal magnetite in the water. We have successfully used sodium lauryl sulphate at a concentration of 0.1% by weight of the magnetite, but other agents and other concentrations might be used.
When aluminium components are present alcng with copper or copper alley (e.g. brass) components in a circulating water system, galvanic corrosion of the aluminium may occur. The method of this invention is effective to reduce or prevent such galvanic corrosion, but only after a period of, perhaps, a few days when a protective layer comprising finely divided particles of magnetite has been formed. Prior to formation of this protective layer, galvanic corrosion may still occur. To prevent this, a supplementary corrosion inhibitor may be included in the circulating water. Copper passivators are well known, and can be used in conventional amounts as supplementary corrosion inhibitors. Examples are sodium mercaptobenzthiazole (smbt) and benztriazole.
It may be convenient to mix the colloidal magnetite with the surface active agent and/or the supplementary corrosion inhibitor before adding the mixture to the circulating water. The colloidal magnetite, optionally in admixture with other ingredients, may be added to the circulating water as a paste, or as capsules or tablets. Preferably the mixture is in the form of capsules coated with water-soluble gelatin.
The following Examples illustrate the invention.

EXAMPLE 1

An aluminium coupon was directly connected to a copper coupon of equal area and immersed in Banbury tapwater at 70°c. The galvanic .current generated by the A1/Cu cell was recorded, and represents a measure of the galvanic corrosion taking place.

i) when no inhibitor was present, a continuing (though fluctuating) current was recorded which did not diminish appreciably with time.
ii) in this test, various amounts of smbt were added, up to the maximum solubility of about 3g/litre. It was found that with 0.5 g/litre or more, the current recorded rapidly fell away with time and after about 90 minutes became negligible, indicating the virtual cessation of galvanic corrosion.
iii) in this test only magnetite was added (1 g/litre) to the water, in this case it was found that the current also fell away, but more slowly than in case ii). The current had come down to negligible values after 2 days. This result is interesting because it provides some confirmation of the observation made above that galvanic corrosion only occurs during the initial stages in a system to which magnetite has been added.
iv) finally, a test was carried out in which both magentite and smbt were added. The current behaviour was similar to case ii) but it was found that inhibition occurred with lower amounts of smbt; in fact 0.2 g/litre was sufficient to give the same result as was achieved with 0.5 g/litre in experiment ii) and a concentration of between 0.2 and 0.5 g/litre was entirely adequate to cause rapid stifling of the galvanic activity. This result is interesting because it indicates that smbt and magnetite have seme kind of "additive" effect in suppressing the galvanic corrosion.

EXAMPLE 2

The comparative experiments of Example 1 were repeated using a test-rig system which simulates the actual use of an aluminium radiator in a circulating water system containing also ccpper pipes and brass fittings. The test-rig experiments confirmed the results of the beaker tests. The radiators were examined after one month's exposure in the simulated central heating system; previous experience had been that, after .one month, some galvanic corrosion would have been observable in the absence of a copper passi- vator.
In the present case, the radiator which had been exposed to water containing 1 g/litre magnetite and 0.5 g/litre smbt showed no signs of corrosion whatsoever. Furthermore the test sample was covered with a very good black film which was determined to comprise hydrated alumina containing embedded therein the colloidal particles of magnetite.

Claims

1. A method of reducing corrosion of the surface of an aluminium or aluminium alloy component in contact with circulating water, which method comprises providing on the surface a protective oxide layer containing finely divided particles of magenetite.

2. A method as claimed in claim 1, wherein the component is of an aluminium-silicon alloy or an alloy of the aluminium-magnesium-silicide group.

3. A method as claimed in claim 1 or claim 2, wherein the component is a hot water radiator in_a heating system.

4. A method as claimed in any one of claims 1 to 3, wherein a source of colloidal magnetite is introduced into the circulating water so as to form on the surface the protective film of magnetite.

5. A method as claimed in claim 4, wherein the source of colloidal magnetite is introduced.intc the circulating water at substantially the same time as the component, whereby there is formed on the surface thereof a protective layer of hydrated alumina containing the finely divided particles of magnetite.

6. A method as claimed in any-one of claims 1 to 5, wherein colloidal magnetite is introduced into the circulating water at.a concentration of from 500 ppm to 10000 ppm.

7. A method as claimed in claim 6, wherein a surface -- active agent is also introduced into the circulating water, in order to assist dispersion of the magnetite in the water.

8. A method as claimed in any one of claims 1 to 7, wherein a supplementary corrosion inhibitor is incorporated to suppress galvanic corrosion of the component in the presence of copper or a copper alloy.

9. A method as claimed in any one of claims 6 to 8, wherein there is introduced into the circulating water at least one capsule or tablet comprising colloidal magnetite and optionally also the surface active agent and/or the supplementary inhibitor.

10. A method as claimed in claim 9, wherein the capsules are coated with water-soluble gelatin.