Background of the Invention
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The problem of preventing the biological growth on ships' hulls, so called fouling, is a serious
one with a considerable economic impact. This growth of biological films, shells, algae and other
species constitute a major drawback in as much as it adds significantly to the water resistance,
reducing speed and adds to the overall costs of propagation. Unhindered growth may also lead
to damage of the hull, causing pitting and corrosion.
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Thus, over the years, several methods have been found to counteract this growth and effectively
prevent it. Although effective these methods still prove insufficient with regards to durability and
long time efficiency, environmental safety, health and security for the people carrying out the
work of preparing the operation of protection as well as further aspects of overall economics.
Antifouling paints.
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Today the most common method of antifouling constitutes of painting the hull with paint
containing one or several toxic substances. Such toxic substances are typically based on
copper, tin or more recently also biocides having a low solubility in water thus leaching only
slowly. Substances of high toxicity have been used but their use has been shown to pose
unacceptable environmental hazards and they have consequently been banned from use in
many countries. Thus today practically all antifouling paints are based on copper-containing and
copper-containing derivatives. The above mentioned high toxicity products had the advantage of
being effective over a range of years whereas the copper-containing based paints in realty
rapidly loose so much of its potency that a new layer of paint have to be applied mostly every
year.
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As the toxic pigments, flakes, particles or components are imbedded in a paint matrix, its rate of
leaching is not constant. The layer exposed to the water is first exhausted, later followed by
deeper laying layers. For this reason the antifouling paints becomes less and less effective with
exposure time. This is particularly true for pleasure boats, many of which spend most of their
time at rest at their moorings. Hence the antifouling is subdued to little attrition and the active
antifouling components have to diffuse through the paint layer to reach the water.
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To compensate for the loss of antifouling efficiency with time, the paint matrix is frequently
made of components permitting the release of the toxic substance when in contact with water.
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The matrix thus assumes an open structure actually absorbing the water and some types, so
called self polishing, dissolves slowly I water. This inevitable and necessary property of
constituting an open structure strongly reduces the paints protective qualities in all other
respects than its antifouling properties. It is well known that such paints offer no protection
against so-called "osmosis", the uptake of water by the polyester laminate, frequently being the
preferred material for boat construction. The antifouling paints, equally, offers no or very poor
additional protection of the hull against mechanical chocks.
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Also, antifouling paints, because of its open structure, are mat, giving the underwater surface a
rough finish. This roughness, which is in the order of 250 microns, adds significantly to the water
resistance and the cost of propelling the vessels.
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The work involved in repainting a ship or boat is a cumbersome one. First the boat or ship has to
be docked or lifted out of water by means of a crane or similar device. Secondly, it has to be
cleaned thoroughly. This is frequently done by high-pressure water jets or by brushing. Any
residual shell or algae growth has to be removed separately or manually. After drying, a
refurbishing of the primary layer of protective paint may be necessary followed by the application
of one or several new coats of antifouling paint. The annual cost for this operation is
considerable, with inconvenience and immobilisation of the vessel not be mentioned.
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The use of antifouling paints is highly questionable also from another, environmental, point of
view. As the hulls need to be repainted regularly, they have to be cleaned and rinsed prior to the
application of a new coat of antifouling paint. Such cleaning is frequently performed with the boat
standing on land. Pleasure boats, for instance, are assigned the same area for "winter" storage
every year and its here that the cleaning takes place. It goes without saying that such an area
becomes heavily polluted from the yearly accumulation of antifouling paint residues and that
such a practice poses a potential risk to the surrounding environment and to the health of people
staying there.
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A further inconvenience with antifouling paints is its property to smear on contact. Whilst the
boat in water, any contact with the antifouling paint will cause smearing of the object with the
paint leaving patches that are difficult to remove. Many have had their ropes, fenders and
bathing suits destroyed by contact with antifouling paint.
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It is clear that a whole range of serious drawbacks and disadvantages accompanies the use of
antifouling paint. Its abundant and common use is solely explained by the present lack of
practical alternatives.
Other methods.
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Before the evolution of shipbuilding permitting to use materials like steel, aluminium or various
plastics, hulls were made of wood. The underwater parts were protected by covering the hull
beneath the water line by nailing sheets of copper by the use of copper nails to the wooden hull.
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Experience using steel nails rapidly proved fatale as the steel nails corroded away within short
and the sheets ran the risk of falling off. The copper-containing plates were thick, to be able to
be handled and hence heavy. However, the antifouling effect was quite satisfactory and lasted
many years although its efficiency diminished with time as a result of the formation of copper
oxides on the surface.
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With the arrival of steel hulls the use of copper-containing plates became impracticable, as no
reliable and yet sufficiently uncomplicated way of attaching the plates to the hull had been
developed. As late as in the 1980es, though, full-scale tests were made using a welding
technique, which is reported to have been successful. (Review of Copper-containing-Nickel Alloy
Sheathing of Ship Hulls and Offshore Structures, Dale T. Peters, Copper-containing
Development Association). No fouling could be detected after several years of use and the
plates had only lost about 10 microns of its thickness per year in spite of its exposure to the high
speeds and prolonged harsh conditions accompanied with the activities of commercial vessels.
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Thus, the use of copper-containing plates is known to constitute an efficient way of protecting
underwater surfaces against fouling. Until now, however, its use has been hampered by the lack
of methods of bonding the copper-containing plates to the surfaces.
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Yet, some attempts have been reported to enable the bonding of copper-containing plates to the
underwater parts. These reported methods all include the prior bonding of the copper-containing
plates to some supporting sheet or layer.
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Two Japanese patents ( EP0562441 and EP0562442) describe a way of using copper or copper
beryllium sheets as antifouling primarily for tubes. The patents claim that the use necessitates
the attachment of an "insulating layer" to the copper sheets. The composite nature of this
product hampers its application on complicated shapes like boot hulls. No reference was given
to the thickness of the sheets, nor to the nature of the bonding.
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The US patent US4987036 describes a method trying to overcome the problem of using
copper-containing sheets to surfaces for their protection against fouling. Also this method
necessitates the prior bonding of the copper-containing sheets to a supporting structure, made
of a mesh, grid or an elastic material, for subsequent bonding of this laminate, using exclusively
a curable neoprene rubber, to the surface to be protected. This method overcomes the problem
of covering curved shapes by first bonding, to the above mentioned supporting structure, narrow
copper or copper nickel sheets comprising a plurality of individual strips of copper or a copper-nickel
alloy in the form of substantially parallelogram in shape.
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It appears that the problem, which has not yet been overcome, is the direct bonding of copper-containing
sheets to surfaces exposed to water and fouling conditions, such as ship or boat
hulls. To add to the problem, copper is a rather heavy metal with a density of 8.4 kg/l. A plate of
4 mm thickness, which was often used during the above-mentioned full-scale tests, thus weighs
a full 33.6 kg/m2. This considerable weight adds to the complications of assuring a firm bonding
of the copper-containing sheet to the surface to be sheeted. The use of epoxy or polyurethane
patty also proved unsatisfactory in the above-mentioned study (Review of Copper-containing-Nickel
Alloy Sheathing of Ship Hulls and Offshore Structures, Dale T. Peters, Copper-containing
Development Association).
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Another factor that may have hampered the use of copper sheets is the subsequent loss of
effectiveness after some time of use. Copper gets oxidised and as this copper oxide layer gets
thicker it appears to loose its antifouling effect. Although this loss in effectiveness usually
becomes apparent only after some years of use the old practice was nevertheless to give the
copper plates a treatment of abrasion or slightly grinding it so as to remove this oxidised layer.
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Thus until now, in spite of the colossal economic impact such a practice would have, no method
has been presented permitting the effective or commercial use of copper-containing sheets for
antifouling purposes for complicatedly shaped surfaces like ship or boat hulls.
Environmental considerations
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Great concern has recently been raised regarding the environmental impact of the use of toxic
antifouling paints. High concentrations of ions of the metals, mostly tin and copper, used in those
paints have been measured in harbours and mooring waters. It appears that the antifouling
paints release their content of toxic substances in an uncontrolled way leading to mentioned high
concentrations. These metal ions have been shown to be absorbed by organisms having a
detrimental effect on their ability to proliferate.
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Particularly worrisome is the fact that antifouling paint releases most of its toxic substances
during the first few weeks the boat is launched into water. This is usually in the springtime when
water organisms are in a delicate phase of their lifecycle. Due to the cold water, first there are
very few of them and secondly they form extremely little fouling during these spring weeks.
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Actually no antifouling would indeed be needed at all during this early period. And during this
time the paints release high amounts of toxic substances. This is a most unsatisfactory state of
affair indeed.
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The problem has been recognised by the authorities in many countries and regulations have
been imposed on the release rate of such metals from antifouling paints. Thus, as an example,
many countries in the European Union has introduced a ban on all tin containing paints for
pleasure boats, although commercial craft may continue to use such paints where however the
release rate must not exceed certain levels.
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Also paints containing copper have been regulated in some countries. In Sweden for exempel,
such paints are not allowed to release more than 200 micrograms of copper per cm2 during the
first 14 days in contact with water as measured by a standardised analytical method. Also other
countries have introduced such restrictions.
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It is interesting to note that the existing antifouling methods in fact do not take into account at all
when they are actually needed.
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For instance, all during the winter period or in cold waters no or virtually no antifouling is required
at all. Equally, it is generally established that when a hull is moving trough water at speed over
2m/sec the biological species fail to adhere to the hull because of the high velocity gradients.
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Also, most algae depend on light for their metabolism so that during the night no antifouling is
needed either.
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On top of all this the existing toxic antifouling methods release lethal doses of toxic metal ions in
spite of the simple fact that the micro-organisms need not be killed at all. Of relevance are only
those organisms that actually cause an increased water resistance for the hull as it moves
through water. Such organisms are seaweed, barnacles and various mussels, for example. They
all have in common to attach to underwater surfaces by means of special organelles excreting
specific proteins (rich in the aminoacid DOPA) which are covalently bonded to the surfaces on
the action of an enzyme complex, which for some species have been isolated as a catechol
oxidase system. These enzymes are denatured by heavy metal ions like tin, mercury, cadmium
and also by slightly higher levels of copper although some copper must be present for the
enzyme to function.
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An efficient antifouling thus only needs to act on the actual attachment phase by blocking these
enzyme systems. Indeed the biochemical reactions leading to fouling takes place in the very
vicinity of the surfaces, probably within a few microns. An antifouling thus has to be active only in
this extremely thin layer thus blocking the adherence of the organisms to the hull.
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Moreover, organisms attachment and growth on surfaces is a slow process. It takes several
days or weeks for these species to grow in size to the extent that their shape may cause
additional drag to a hull. It thus seem completely unnecessary to release toxic substances
continuously when intermittent protection depending on circumstances would be more than
appropriate.
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In fact, it has until now been generally agreed that copper antifouling is effective as a result of
the release of copper ions. However, the present invention completely contradicts this general
belief in so far as antifouling was achieved without any measurable loss of copper from the
copper-containing layers or sheets.
Description of the invention.
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The present invention describes a method, a product and its application, permitting an effective
and practical use of copper-containing conductive layers to counteract biological fouling on any
surface including complicatedly shaped surfaces such as boat-or ship hulls in particular.
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The new method completely eliminates the detrimental effect on the environment normally
resulting from antifouling active substances.
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The method offers a breakthrough in the way the antifouling effect can be controlled as the effect
can be "switched" on and off in line with the need for antifouling.
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The copper-containing conductive layer may be constituted of plates, sheets, foils, grid or mesh
or smaller pieces such as flakes of such applied so as to form a conductive layer.
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The method moreover overcomes the difficulties of bonding copper-containing sheets to
surfaces, curved in three dimensions.
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The method also and additionally provides further protection of the underwater surfaces against
damages caused by the surfaces contact with water such as so called osmosis and the method
adds to the strength of the structure and its resistance to mechanical shock.
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The use of the method further reduces the roughness of the hulls thus permitting improved fuel
economy or higher speeds.
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The protected surface, moreover, becomes essentially smear-free thus offering enormous
advantages both when it comes to handling of the protected surface and the almost total
absence of environmental impact when cleaning.
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The method provides protection from fouling over a period of several years.
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In fact the solution to the previously described problems of sheathing is the following:
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By protecting the copper from corrosion the use of very soft and very thin copper-containing
sheets may be used. Yet thick enough to last several years under harsh marine conditions and
to give long-term protection against fouling, these sheets can successfully be shaped and
bonded to any surface without the use of welding, fasteners like nails or prior bonding to
insulating layers, supporting films or structures. Equally, the use of such thin sheets avoids the
otherwise necessary use of narrow strips to cover complicated shapes.
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As thin copper-containing sheets are light-weight its bonding to the surfaces to be protected
becomes much less complicated. Such thin sheets are basically held in place by the action of
the hydraulic pressure exerted on it by the water, provided that no water is allowed to trickle in
between the sheets and the hull. In fact this surprisingly simple idea permit the use of most
commercially available water resistant adhesives suitable for the bonding of copper-containing
onto the surface in question to be protected. These copper-containing sheets are so lightweight
that the pressure exerted by the depth of water helps to keep them in place, easing the strain on
the bonding adhesive.
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The problem of loss of efficiency over the years as a result of the formation of an oxidised layer
is also overcome by the use of anticorrosion measures. By rendering the copper surface
cathodic no oxidation can take place and the surface remains in its copper metal state. Such
methods are in common use to protect principally steel constructions from corrosion and are
known as "cathodic protection". Such cathodic protection can be achieved either by assuring a
metallic contact between the metal to be protected and a so called sacrifice anode, made by a
less noble metal, mostly zinc or aluminium, or by applying a source of electricity in the form of a
direct current thus rendering the surface to be protected passivated or immunised.
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Attempts have been reported to counteract the corrosion of copper in seawater by using such
cathodic protection but they were quickly abandoned as it was noted that the antifouling effect
disappeared.
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In this invention, such cathodic protection is nevertheless employed as it was surprisingly
observed that removing the cathodic protection for short periods of time restored the antifouling
effect without loosing any of the protection regarding corrosion. This particularly interesting
aspect of the invention offers a completely unique and novel method to prevent fouling without
any environmental impact whatsoever.
Detailed description of the invention.
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It was felt that not enough consideration had been taken to ensure a practical use of copper-containing
sheets for boat-or ship coating. Thus a copper-containing sheet must be so soft as to
be able to follow the geometry of the surface to be sheeted regardless of its shape. Hence a
very thin sheet or foil indeed should be used. To ensure a permanent bonding to the surface to
be sheeted, it must in fact be so soft as to form essentially watertight agglomerate with the
surface so that no or very little water may trickle in between the copper-containing sheet and the
surface.
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Copper-containing materials are heavy and thick plates may not become sufficiently bonded to
withstand its tendency to fall down by its own weight. Also this is avoided using very thin sheets
or foils. Such thin sheets may basically be held in place by the hydrostatic pressure exerted on
them by the water pressure, provided that essentially no water is permitted to enter between the
surface to be protected and the copper-containing sheet itself. Such close contact can be
achieved by the use of one or several commercially available adhesives.
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However, copper containing sheets not protected against corrosion must not be too thin. They
should, of course, be sufficiently thick so as not to corrode away too quickly, making the use
impractical. As it has been reported that, under realistic conditions on commercial vessels, the
rate of corrosion is in the order of 10 microns per year, the practical absolute minimum thickness
would thus be some 50 microns.
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The copper-containing sheet must additionally have properties such as to permit its firm bonding
to the surface to be sheeted. Also this is facilitated by the use of very thin and soft sheets.
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Copper-containing materials have a high thermal expansion coefficient, which differs much from
that of the materials normally used for ship-and boat hulls. A thin and soft copper-containing
sheet exerts less global strain on the bonding than a thick one as the temperature changes.
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Likewise, which has been totally neglected in previous attempts, the surface to be coated must
also be prepared so as to enable its sheathing. Also this aspect is covered by the new invention.
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Finally, to be practical, the sheathing must be reversible, i.e. some day, eventually, all hulls must
be refurbished and the removal of the sheathing must not be virtually impossible, risk to destroy
the hull itself or otherwise cause damage to it. One aspect of the new invention takes full
account of this most important aspect.
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In one aspect of the present invention, thin, soft copper-containing sheet or foil is bonded
directly, without the need for supporting films or structures, to the curved surfaces to be
protected by the use of any commercially available adhesive suitable for the water resistant
bonding of copper-containing onto the surface to be protected. Because of the softness and the
low weight of such thin copper-containing foils the strain on the bonding is low and the bonding
itself, with the proper selection of adhesive, becomes stronger than the foil itself. The practical
thickness of the foils was found to be in the range of 10 to 250 microns.
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In a further aspect of the invention, thin copper-containing sheets or foils can be prepared in
advance with a water-resistant adhesive, which can be activated at a later time when the actual
sheathing is to take place. Such adhesives can be any of the types found among the group of
"tapes", known under the commercial names as "Scotch", "Tesa" etc. Such adhesives are
frequently derivatives of acrylics but the invention is in no way limited to the use of such acrylics
as any water-resistant adhesive can be used. The foils may thus be prepared in advance to form
a composite tape where the adhesive side would be covered by a so-called release cover to be
removed just prior to the sheathing. Also other suitable adhesives can be used as those
activated by heat, solvents or other methods.
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In yet another aspect of the invention, thin copper-containing sheets can be used to constitute
an integral part of a ship's or boat's hull. Boats made of glass fibre reinforced resins, like
polyester, epoxy etc. are produced by laminating the fibreglass with the resin in moulds. When
the laminate has hardened and cured, the mould is removed and the hull is then fitted with such
further details as to make it complete. The bottom must then be painted with antifouling.
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However, the present invention facilitates the completion of the hulls. In this aspect of the
invention, the copper-containing sheet is first placed on the part later of the mould later to hold
the underwater part of the hull, then the laminating proceeds as usual, taking into full account to
use a laminating resin having a sufficient adhesion to the copper-containing foil. When the
laminate has hardened and cured and the mould has been removed, the hull already has its
underwater part sheathed with the copper-containing sheet. In this way the finished hull will have
an incorporated antifouling treatment. The same technique can be used for any item, produced
in moulds and which should possess antifouling properties
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In one especially efficient aspect of the invention, the copper-containing sheets are mounted to
the surface in such a way as not to expose any edge of copper-containing sheet to the main
direction of the water flow. This may be achieved by ensuring to overlap the sheets
"downstream" thus effectively reducing the risk of the sheets being peeled off by the action of
the flow of water over the surface when the vessel is making headway.
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A breakthrough in antifouling technique is offered in the aspect of the invention where the
antifouling effect can be controlled as to coincide with the need to prevent fouling. Copper
metals in contact with natural water having slightly basic pH values may exist in three distinct
states: At a low enough redox potential copper shows immunity and no corrosion occurs.
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Secondly, at higher redox potentials, copper can also be in a passive state which is also
corrosion free but an oxidation to Cu2O or CuO occurs on the surface. Thirdly, full corrosion
occurs at high redox potentials, low or high pH values and in the presence of anions like
chloride. Copper is in this state released as Cu 2+ or CuO2 2- ions. Which state copper is in is
thus a function of its redox potential. Copper in its immune state is inert and does not corrode
which is favourable but on the other hand does not offer any antifouling properties either. The
passive phase or state is antifouling active but a layer of copper oxides develops, grow thicker
and the antifouling diminishes with time. This invention relates to alternating between these
states.
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The transition from immune to passive and visa versa can be controlled. Such a controlled
effect can be established by the connection of an sacrifice anode, made of a metal less noble
than copper, to the copper containing sheet in such a way that said connection may be
disconnected at intervals. As an example the anode may be connected to the copper sheets by
means of a circuit via a switch, which can be closed or opened. When the switch is open the
anode is not electrically in contact with the copper-containing conductive layer or sheet and thus
the copper is in an active phase as to what corrosion concerns. However, when the switch is
closed, the anode is again connected to the copper sheet and the cathodic protection is
restored. Said switch may be operated by a timer or other device so as to regulate the time
intervals. The same effect can be achieved by mechanical means, making the anode alternating
between being physically in contact with the copper sheet and not in contact. A third possibility is
to use an applied current from a separate current source.
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This particularly effective method ensures that the copper containing sheathing remains
antifouling-effective as no oxide layer develops and on the same time the copper surface is fully
protected from corrosion.
Example 1.
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A piece of copper foil, 100 micrometers thick, was weighed accurately, connected with a cable
via a timer-controlled switch to an aluminium rod and the copper and the rod were subsequently
immerged in seawater maintained at approximately 20 deg C with a salt content of 3%. The
timer was set to close the circuit for 45 minutes and disconnect the aluminium anode from the
copper sheet for 15 minutes, this cycle repeating every hour. The copper sheet was weighed at
intervals and the biological growth observed.
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The result was very surprising.
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No corrosion at all could be detected as the copper remained oxide free but lost no weight. No
fouling occurred either even after four months exposure, showing that the surface remained
nevertheless active in protecting against fouling.
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A control piece of inert Teflon was covered by a thick layer of algae. Another control piece of
copper foil without any cathodic protection was equally covered by a layer of algae.
The table below shows the test results.
Days | Loss (Calculated as µm/year from start of test) |
4 | 1.8 |
8 | -6.7 |
14 | -6.7 |
27 | 0.1 |
59 | 0.1 |
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As can be seen no weight loss calculated as loss in thickness per year due to corrosion could be
noticed during a 60 days of trial. The irregularity and the negative signs were due to some
accumulation of mineral particles on the copper sheet which was not cleaned until on the 59th
day so as to permit an inspection of possible biological fouling.
Example 2.
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It was surprisingly found that copper-containing foil as thick as typically 100 micron of the soft
quality, supplied by the company Outokompu, Västeras, Sweden could be shaped to follow any
curvature present on boat hulls. This thickness would correspond to about ten years of heavy
use, a considerable advantage compared to antifouling paint practice of repainting mostly every
year. The roughness of the copper-containing foil was in the order of 5 microns.
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It was also surprisingly found that this relatively thin foil, after having been cleaned from grease,
loose oxides and dust, permitted a strong adherence to surfaces using simple "neophrene
contact" glue", commercially available from the companies 3M, Henkel and others.
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Thus a surface (in the form of a centreboard keel) was sheathed using the above-mentioned
method. To ensure an optimal adherence, the surface to be protected was prior to the sheathing
painted using a two component polyurethane paint. Several such paints are commercially
available. It was not considered vital to use polyurethane paints and any water-resistant paint
giving a reasonably even and smooth surface would give the same result.
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Surfaces so prepared were subdued to severe testing including twenty cycles of consecutive
freezing and prolonged, 48 hours, exposure to 40 °C warm salt-water. The surface was equally
subjected to 80 bar water jet cleaning. Neither of these conditions led to any visual separation of
the copper-containing foil from the surface.
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Then the surface was mounted under water on a boat in order to evaluate its properties under
real conditions. After one full year of service no sign of release or separation was to be detected
and the surface remained essentially free of fouling.
Example 3.
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It was even more surprising to find that, using such copper containing foil as in example 1, even
so called "sticking tape" (known commercially as Scotch, Tesa etc.) provided sufficiently strong
bonding.
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The surface to be protected was first prepared in the same way as in example 1 but using a
glossy paint.
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Normally boat and ship hulls are painted on their underwater parts using mat primer paints,
which offers a better base for the subsequent application of antifouling paints. However, it was
found that copper-containing sticking tape adhered just as well to glossy paint.
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As the paint had cured, the surface of the hull to be studied was first clad with the double-sided
tape (so called adhesive transfer tape available from the company 3M) making sure to cover the
entire underwater surface and a band some decimetres above the waterline. The protective film
facing the outside was left in place.
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Then after successive removal of the protective film, the copper-containing-containing foil was
pressed firmly, against the adhesive tape by the aid of a rubber roller. Care was taken not to
enclose any air under the copper-containing-containing foil. Thus the work proceeded until the
entire surface, to be studied, was covered. Although glossy paint was used in this example, the
invention is in no way limited to the use such paint as also mat paint gives satisfactory results.
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The fact of using a sub millimetre sheet, which was not heavy, made the work possible giving a
most satisfactory result essentially without wrinkles. In fact, a ship or boat hull must be very
smooth and even so as to exert the minimum of resistance when the ship makes way.
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The boat was then launched.
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The water exerts a hydrostatic pressure (depending on the depth beneath the water surface) on
the hull. As the copper-containing-containing sheathing was so thin and the fact that its weight
was only 0.84 kg per m2 the hydrostatic pressure actually counteracted the weight of the
copper-containing sheathing so that in theory no further bonding would be required under static
conditions, which explains why such a relatively unqualified adhesive turned out to have
sufficient bonding strength. However, a boat or ship does not stay at rest and the water swirling
by, when the hull makes headway, exerts a force on the sheathing. To avoid "peeling" off of the
sheathing, it was applied in such a way as to ensure that all overlapping of the sheets was done
"downstream" i.e. the surface was clad from stern to bow.
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In one case, a band of such metal tape remained firmly attached to the boat hull after 17 full
years!
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It thus appears to be much less complicated than generally thought to adequately bond copper-containing-containing
sheets to a boat or ship hull.
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The copper-containing-containing sheet could be easily removed by heating the sheet by means
of a hot air gun and a scraper.
Example 4.
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As in example 1, the surface to be sheeted was first prepared by proper cleaning, sanding and
painting with a polyurethane paint.
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Separately, a copper-containing sheet, 100 microns thick and from the same supplier, had been
washed and treated to ensure the removal of grease and loose oxides. After drying, the double-sided
transfer tape was applied to the copper-containing sheet, leaving the protective outer film
intact.
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The protective film was then removed and the copper-containing sheet, with its transfer tape,
was pressed against the surface of the boat hull by means of a rubber roller.
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Also this procedure gave a most satisfactory result.
Example 5.
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The surface to be protected was prepared in the same way as in example 1, 2 and 3. The
surface was then coated with a heat sensitive adhesive tape, available from 3M Company. Such
tapes perform like ordinary tapes but their bonding properties can be much improved on heating
the substrate after the initial bonding. Thus the copper-containing sheet was applied in the same
way as in example 1 and 2 but the surface was later heated using an electrically heated "iron"
device so as to cure the bonding according to 3M's specifications.
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This treatment resulted in an equally solid bonding. Subsequent attempts to remove the
sheathing, with the aim of simulating a major overhaul, proved difficult, as the bonding was very
firm indeed. New sheathing could therefore be made on top of the existing one.
Example 6.
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A mould, normally used for the production of boat structures, was first clad with the thin copper
foil on the part to be under water in the finished hull. Then, on top of the copper foil, this area
was laminated using epoxy resin and a thick glass fibre weave, commercially readily available.
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The lamination then preceded using resin and fibreglass in the usual manner until the part was
finished. After release from the mould, the part of the structure, to be submerged, was thus
sheathed with the copper foil.