[0001] This invention relates to the corrosion protection of pipes, vessels and other corrodible
substrates.
[0002] It is well known to protect substrates from corrosion by establishing a corrosion-protecting
potential difference between the substrate and a counter-electrode. Preferably a DC
power source is used to establish the desired potential difference between the substrate
as cathode and an anode which is composed of a material which is resistant to corrosion,
eg. platinum, graphite, or a conductive polymer. Reference may be made for example
to U.S. Patents Nos. 3,5l5,654 (Bordalen), 4,502,929 (Stewart et al), 4,473,450 (Nayak
et al), 4,3l9,854 (Marzocchi), 4,255,24l (Kroon), 4,267,029 (Massarsky), 3,868,3l3
(Gay), 3,798,l42 (Evans), 3,39l,072 (Pearson), 3,354,063 (Shutt), 3,022,242 (Anderson),
2,053,3l4 (Brown) and l,842,54l (Cumberland), U.K. Patents No. l,394,292 and 2,046,789A,
Japanese Patents Nos. 35293/l973 and 48948/l978, and European Patent Publication No.
0l479777.
[0003] The known corrosion systems suffer from serious disadvantages, in particular a failure
to obtain sufficiently uniform current distribution on the substrate. This disadvantage
can arise from the use of one or more discrete electrodes; or from the use of a distributed
electrode, eg a platinum wire, whose radial resistance to the substrate is low, so
that at high currents the current density on the anode decreases rapidly as the distance
from the power source increases; and/or because the substrate is shielded (including
those situations in which the substrate has a complex shape which results in one part
of the substrate being shielded by another part of the substrate). The flexible elongate
anodes disclosed in U.S. Patents Nos. 4,502,929 and 4,473,450, which comprise a low
resistance core surrounded by a conductive polymer coating, are very useful in mitigating
this disadvantage, but they cannot be used at the high current densities which are
required in certain situations, for example the protection of structures which have
no protective coating thereon. Another disadvantage is the relatively short life of
anodes (including the electrical connections thereto), especially when exposed to
environments which are highly corrosive or which contain oily contaminants (and in
the case of platinum anodes, when exposed to fresh potable water), and the difficulty
and expense of repairing or replacing the anodes when this becomes necessary.
[0004] We have now discovered that these disadvantages can be mitigated or overcome by means
of a barrier which lies between the substrate and the counter-electrode, which is
spaced part from the substrate and the counter-electrode, and which directs the flow
of ions between the substrate and the counter-electrode, and thus provides an improved
current distribution on the substrate, and/or enables the counter-electrode to be
more easily maintained or replaced, and/or reduces the rate at which the current density
on an elongate electrode changes with the distance from the power source, and/or provides
a controlled environment around the electrode to improve its efficiency, eg. by reducing
contamination or by making it possible to surround the counter-electrode with an electrolyte
which is different from the electrolyte which contacts the substrate.
[0005] In one aspect, the present invention provides an assembly for cathodically protecting
an electrically conductive substrate from corrosion, and a method of corrosion protection
which makes use of such an assembly, the assembly comprising
(l) an electrically conductive substrate which is liable to corrosion;
(2) an elongate distributed anode, ie. an anode which has a shape corresponding generally
to the shape of the substrate and which is relatively close to all points on the substrate;
and
(3) a barrier which (i) lies between the substrate and the anode, (ii) is spaced apart
from the substrate and from the anode, and (iii) is in the form of a tube which surrounds
the anode and has a plurality of ion-permeable sections therein such that, when the
anode and the substrate are electrically connected to opposite poles of a DC power
source and are electrically connected by means of an electrolyte, the barrier restricts
the flow of current between the substrate and the anode so that the resistance between
the substrate and the anode is Q times the resistance between them in the absence
of the barrier, where Q is at least l.5.
[0006] In another aspect, the present invention provides a method of cathodically protecting
an electrically conductive substrate from corrosion by an electrolyte which contacts
it, which method comprises establishing a potential difference between the substrate
and a discrete anode which is located in an anode chamber containing an electrolyte
and having at least one ion-permeable section therein, the electrolyte being fed into
the chamber and being driven by hydrostatic pressure from the chamber through said
at least one ion-permeable section.
[0007] The barrier which is used in the present invention modifies the way in which current
flows between the substrate and the anode so as to produce one or more of the desirable
results noted above. In general, this will result in the resistance between the substrate
and the anode being substantially higher than it would be in the absence of the barrier,
preferably by a factor of at least l0, for example at least l00, or even more, balancing
the resulting advantages against the disadvantage of the higher voltages required
as the resistance increases.
[0008] The barrier preferably comprises a plurality of ion-permeable sections. Preferred
ion-permeable sections include simple apertures, for example a hole in the wall of
a tube, or an opening at the end of a tube. Ion-permeable sections which are composed
of an ion-permeable material, eg. a glass frit, can also be used, especially when
it is desired to have the anode contacted by an electrolyte which is different from
that which contacts the substrate. The size and/or the spacing of the ion-permeable
sections can be uniform or non-uniform, depending upon the desired current distribution
on the substrate. The ion-permeable sections are preferably of fixed dimensions. The
distance between adjacent ion-permeable sections is preferably less than l0 times,
particularly less than 4 times, the distance between the ion-permeable sections and
the substrate. An important factor in determining the size of the apertures can be
the need to ensure that anodic reaction products, eg gaseous chlorine, do not block
the apertures. Unless the conditions of operation are such that anodic reaction products
remain dissolved in the electrolyte or can be easily vented, care must be taken to
prevent harmful build-up of such reaction products between the anode and the barrier.
In some case positive benefit can be derived from such reaction products, eg. to lessen
fouling of marine structures. To assist in the dispersion of such reaction products,
it is preferred to operate the system in such a way that hydrostatic pressure drives
the electrolyte through the ion-permeable section(s) towards the substrate. Such hydrostatic
pressure, which is typically provided by a pump, can have the alternative and/or additional
advantages of (l) reducing the danger that the ion-permeable sections will be blocked
by contaminants present in the electrolyte between the barrier and the substrate,
for example oily contaminants in the water layer at the bottom of an oil storage tank,
and/or (2) making it possible, when it is desired to surround the anode with an electrolyte
which is different from the electrolyte which contacts the substrate (eg. when protecting
a potable water tank with a platinum anode), to prevent substantial contamination
of the anode electrolyte by the substrate electrolyte with minimal contamination of
the substrate electrolyte by the anode electrolyte.
[0009] The barrier must not be electronically connected to the substrate or the anode, and
is preferably composed of (including coated by) an electrically insulating material,
eg. a plastic. Preferred barriers are in the form of a tube (which may be of round
or other cross section) or a plurality of tubes which are joined together to form
a branched structure. In such a branched structure, the branch tubes are preferably
of smaller cross-section than the main tube, for example so that the total cross-sectional
area of the branch tubes is no greater than the cross-sectional area of the main tube.
The tube or tubes can be heated by an internal or external heater to reduce the viscosity
of the electrolyte therein (including to prevent it from freezing) and/or to reduce
its resistivity. The tube or tubes can be arranged as a continuous loop, so that electrolyte
circulates through them, or can simply terminate in an open end (ie. an ion-permeable
section) or a closed end.
[0010] In a particularly preferred embodiment, the tube (or at least one of the tubes where
a plurality of tubes are joined together) surrounds an elongate anode, for example
one whose length is at least l00 times, preferably at least l000 times, its smallest
dimension, typically a metal wire, especially a platinum or platinum-coated wire,
having for example a diameter of at least 0.0l inch (0.025 cm), preferably 0.02 to
0.3 inch (0.05 to 0.075 cm). The internal diameter of the tube containing the wire
anode is preferably P times the diameter of the wire, where P is 2 to l00, eg. 5 to
30, for example a diameter of 0.l25 to 0.6 inch (0.36 to l.5 cm). The tube containing
the wire anode comprises ion-permeable sections, or there are branch tubes comprising
ion-permeable sections attached thereto, or both. The branch tubes can comprise perforations
and/or can have an open end, which may be fitted with a nozzle. In this way, it is
possible to obtain a much more uniform current density on the anode, and hence also
on the substrate, than in the absence of the barrier. This desirable result is achieved
because the resistance between the substrate and the elongate anode is much greater
than it would be in the absence of the tube or tubes, preferably by a factor of at
least l0, for example at least l00 or even higher. This is especially valuable when
it is desirable to provide a high current from a distributed anode. Under these circumstances,
it is not satisfactory to use an anode comprising a metal core and a conductive polymer
jacket, because such anodes cannot support the high current densities required. Nor
is it satisfactory to use a platinum wire anode (or the like); such anodes will support
very high current densities, but at the currents needed in such circumstances, the
current density on the anode decreases rapidly as the distance from the power source
increases, as demonstrated for example in Example 2 below.
[0011] In another preferred embodiment, the anode is a discrete electrode which is placed
in a vessel remote from the substrate, and electrolyte is pumped (or gravity fed)
from the anode vessel to the vicinity of the substrate
via one or more tubes which constitute the barrier and which contain (including terminate
in) ion-permeable sections. In such a system, it is important that the resistance
of the electrolyte in the tube or tubes should not be too high. Therefore, the resistivity
of the electrolyte is preferably less than 50 ohm.cm, particularly less than 20 ohm.cm,
so that the tubes can be of a convenient size. In this embodiment, the main tube or
tubes conveying electrolyte from the anode chamber to the vicinity of the substrate
may for example have an equivalent inner diameter (ie. of cross-section equal to a
circle of that diameter) of l to l2 inches (2.5 to 30.5 cm), and the branch tubes
may for example have an equivalent diameter of 0.5 to 3 inches (l.25 to 7.5 cm).
[0012] Any appropriate DC power source can be used in the present invention. The voltage
of the power source is preferably less than l00 volts, particularly less than 50 volts,
with the system being designed with this preference in mind.
[0013] When there is a net transfer of electrolyte through the ion-permeable section(s)
of the barrier, electrolyte must be supplied to the anode, and this can be done by
recycling electrolyte from the vicinity of the substrate and/or by supplying fresh
electrolyte. When build-up of electrolyte in the vicinity of the substrate must be
avoided, eg. in the bottom of an oil storage tank, means must be provided for removing
excess electrolyte; the excess electrolyte can be recycled to the anode, if desired
or necessary after filtering or otherwise treating it to remove harmful contaminants.
[0014] Preferred uses for the present invention include the protection of city water tanks,
ballast tanks in ships, oil rigs, cooling tanks for power stations, water tanks for
secondary recovery in oil wells, oil storage tanks, heat exchangers, condensers, heater
treaters, and buried pipes, in particular pipes buried below the permafrost line,
for example oil pipes in frozen tundra.
[0015] Referring now to the drawing, each of Figures l and 2 shows a DC power source l which
is connected to an anode 2 and a corrodible substrate 3 which is a cathode. Anode
2 and substrate 3 are separated by a barrier 4 which comprises ion-permeable sections
45, and are connected by electrolyte 5 through sections 45. A positive hydrostatic
pressure is maintained from the interior of the barrier 4 across the ion-permeable
sections 45 by means of pump 6.
Figure l is a diagrammatic side view which shows the corrodible substrate 3 within
a vessel 7 containing the electrolyte 5. The anode 2 is an elongate anode, and the
barrier 4 is a perforated tube containing the anode.
Figure 2 is a diagrammatic side view in which the substrate 3 is an oil storage tank
in which the electrolyte 5 is a highly corrosive aqueous mixture covered by oil 8.
The anode is a discrete anode which lies within an anode chamber 2l. The barrier 4
comprises, in addition to the part of the anode chamber which lies between the anode
and the tank 3, a tube 4l which leads from anode chamber 2l to the center of tank
3 and branch-tubes 42 which communicate with tube 4l, which are of relatively small
diameter, and which contain perforations 45. Means not shown removes excess electrolyte
from the tank 5. Pump 6 maintains a positive pressure across the perforations 45 and
thus reduces the danger that they will become blocked by oily contaminants in the
water layer.
Figure 3 shows in diagrammatic plan view an alternative way of protecting a vessel
3. Tube 44 surrounds the vessel and contains elongate anode 2. Branch tubes 42 communicate
with tube 44, pass through the wall of the vessel, and terminate in open ends or nozzles
45 which can point in one or more desired directions.
Figure 4 shows in diagrammatic side view a system for protecting a pipe 3 which is
buried in the earth or immersed in the sea or other electrolyte. The anode 2 lies
within an anode chamber 2l and is surrounded by electrolyte 3. Barrier 4 comprises
a tube 4l which extends downwards from the anode chamber 2l and branch tubes 42 which
communicate with and extend horizontally from the tube 4l under the pipe 3, and which
comprise nozzles 45 covered by protective caps. Tube 4l contains a heater 9 which
may be used to prevent the electrolyte from freezing or reduce its viscosity, for
example when the tube 4l passes through a layer of earth which is frozen or liable
to freezing, and/or to decrease its resistivity. A positive hydrostatic pressure is
maintained across the nozzles 45, and the electrolyte lost in consequence is replaced
from electrolyte storage tank 23.
Figure 5 shows a tube with perforations therein through which ion-containing electrolyte
can emerge; the perforations shown are uniformly spaced and of uniform size, but they
could be of different sizes and separations in order to provide desired current distribution.
Figure 6 shows a tube composed of an ion-conducting membrane through which ions can
pass, but non-ionic material cannot.
Figure 7 shows a perforated tube which is covered by an ion-conducting membrane.
Figure 8 shows a part of a perforated tube in which each perforation is covered by
an ion-conducting membrane.
Figure 9 shows an open-ended tube through the open end of which ion-containing electrolyte
can emerge.
Figure l0 shows an open-ended tube whose open end is covered by a porous plug.
Figure ll shows a tube having a plurality of branch nozzles mounted thereon.
Figure l2 shows the arrangement of the tube in Example l, as described below.
[0016] The invention is illustrated in the following Examples.
EXAMPLE l
[0017] In this Example, procedures (A) and (B) are comparative Examples, and procedure
(C) is an example of the invention.
(A) An l8 × 24 inch (45.7 × 6l.0 cm) stainless steel mesh screen was placed on the
bottom of a tank. One end of each of six flexible plastic tubes 0.375 inch (0.95 cm)
inner diameter × 6 foot (l82.9 cm) long was positioned about l inch (2.5 cm) from
the screen; the ends of the tubes were placed in a rectangular pattern centered over
the screen as illustrated in Figure l2, with x being 4.5 inch (ll.5 cm) and y being
4 inch (l0.2 cm). The other end of each tube was placed in a second tank adjacent
the first. The tubes and both tanks were filled with 3% NaCl solution having a resistivity
of about 20 ohm.cm. A saturated calomel electrode (SCE) was placed in the first tank
in a number of different positions so that the potential of different parts of the
screen could be measured. The corrosion potential of the screen was measured to be
0.220V, and was uniform across the screen surface.
(B) The apparatus described in (A) was modified by placing a single graphite anode
l inch (2.5 cm) above in the center of the screen. The anode and the screen were connected
to a DC power source of sufficient voltage to maintain a total current of 0.05A. The
absolute potential of the screen (i.e. the potential measured by the SCE minus the
corrosion potential) was found to be at a maximum of 0.560V. The absolute potential
decreased in a radial pattern away from the anode, reaching 0.499V at the edge of
the screen, a total difference of 0.06lV.
(C) The apparatus described in (A) was modified by placing a single graphite anode
in the second tank. The anode and the screen were connected to a DC power source,
and with the tubes acting as salt bridges between the tanks, sufficient voltage (about
45 VDC) was applied to maintain a total current of 0.05VA. The absolute potential
of the screen was found to be at a maximum of 0.550 - 0.563V directly below each of
the tube openings and at a minimum of 0.540V at the edges of the screen, i.e. a difference
of at most 0.023V as compared to a difference of at most 0.06lV in (B) above.
EXAMPLE 2
[0018] In this Example, procedures (A) and (B) are comparative examples and procedure (C)
is an example of the invention.
(A) A plastic trough about l8 feet (5.5m) long and of semi-circular cross-section,
diameter 4 inch (l0.2 cm), was connected by means of a drain to a plastic tank containing
a submersible pump. The trough, the tank and the drain were filled with aqueous potassium
chloride electrolyte of resistivity 20.5 ohm.cm. A mild steel rod about l8 feet (5.5m)
long and 0.5 inch (l.25cm) in diameter was placed in the bottom of the trough. A plastic
tube about l8 feet (5.5m) long, 0.375 inch (0.95 cm) in inner diameter and 0.5 inch
(l.25 cm) in outer diameter was secured to the wall of the trough, parallel to the
mild steel rod and spaced apart from it. The plastic tube comprised holes 0.0l0 inch
(0.025 cm) in diameter every 3.94 inch (l0 cm) along a straight line, and the tube
was secured to the trough so that the holes were 0.75 to l inch (l.9-2.5cm) from the
mild steel rod. One end of the tube was connected to the submersible pump in the tank
and the other end was sealed. The pump was used to pump electrolyte through the tube.
Excess electrolyte returned from the trough to the tank through the drain. A saturated
calomel reference electrode (SCE) was placed in the trough in a number of different
positions so that the potential of different parts of the rod could be measured. The
corrosion potential of the rod was measured to be between 0.626 and 0.699V, an average
of 0.655V.
(B) The apparatus described in (A) was modified by securing a platinum wire anode
0.0l0 inch (0.025 cm) in diameter and about l8 foot (5.49m) long to the surface of
the plastic tube so that the anode was 0.75 to l inch (l.9 to 2.5 cm) from the rod.
The rod and one end of the anode were connected to a DC power source of sufficient
voltage to maintain a current of 0.5 amp. The absolute potential of the rod (i.e.
the potential measured by the SCE minus the corrosion potential) was found to be 0.62V
at the end which is adjacent the end of the anode connected to the power source, and
to decrease to 0.05V at the other end, a total difference of 0.57V.
(C) The apparatus described in (B) was modified by placing the anode inside the plastic
tube. The power source was adjusted to provide a current of 0.5 amp, and the pump
was adjusted to provide a flow rate which ensured that the holes in the tube were
not plugged by the gaseous products evolved at the anode (i.e. chlorine and oxygen).
The absolute potential of the rod was found to be between 0.40 and 0.55V, i.e. a total
difference of 0.l5V.
1. An assembly for cathodically protecting an electrically conductive substrate from
corrosion, the assembly comprising
(l) an electrically conductive substrate which is liable to corrosion;
(2) an elongate distributed anode which has a shape corresponding generally to the
shape of the substrate; and
(3) a barrier which (i) lies between the substrate and the anode, (ii) is spaced apart
from the substrate and from the anode, and (iii) is in the form of a tube which surrounds
the anode and has a plurality of ion-permeable sections therein such that, when the
anode and the substrate are electrically connected to opposite poles of a DC power
source and are electrically connected by means of an electrolyte, the barrier restricts
the flow of current between the substrate and the anode so that the resistance between
the substrate and the anode is Q times the resistance between them in the absence
of barrier, where Q is at least l.5, preferably at least l0, particularly at least
l00.
2. An assembly according to claim l wherein the length of the anode is at least l00
times, preferably at least l000 times, its smallest dimension, and the barrier is
in the form of a tube which is composed of an insulating material, and which has apertures
in the walls thereof.
3. An assembly according to claim l or 2 wherein the barrier further comprises a plurality
of branch tubes, each of the branch tubes communicating with the tube and having at
least one aperture therein.
4. An assembly according to claim l, 2 or 3 wherein the anode is a metal wire having
a diameter of 0.05 to 0.75 cm. and the internal diameter of the tube is P times the
diameter of the wire, where P is 2 to l00, preferably 5 to 30.
5. An assembly according to any of the preceding claims wherein the anode has a platinum
surface.
6. An assembly according to any of the preceding claims wherein the assembly further
comprises a pump for pumping liquid electrolyte down the tube and through the ion-permeable
sections towards the substrate.
7. A method of cathodically protecting an electrically conductive substrate from corrosion
by an electrolyte which contacts it, which method comprises establishing a potential
difference between the substrate as cathode and a discrete anode which is located
in an anode chamber containing an electrolyte and having at least one ion-permeable
section therein, the electrolyte being fed into the chamber and being driven by hydrostatic
pressure from the chamber through said at least one ion-permeable section.
8. A method according to Claim 7 wherein the substrate is buried in soil, the electrolyte
is driven into the soil, and the anode is located in an anode chamber which is accessible
from above ground, so that the electrode can be easily maintained or replaced.
9. A method according to Claim 8 wherein the substrate is buried below a permafrost
line in the soil and the ion-permeable section is below the permafrost line.
l0. A method according to Claim 7 wherein the substrate is contacted by a mass of
liquid electrolyte, for example the sea, and the anode is located in an anode chamber
which is accessible separately from the mass of electrolyte so that the electrode
can be easily maintained or replaced.