[0001] This invention relates to the heat treatment of metals. In particular, it relates
to the heat treatment of metals which are less readily oxidisable than iron. Such
metals include cobalt, nickel, lead, copper, palladium, silver and gold, alloys of
such metals, and alloys of mercury.
[0002] In manufacturing articles made of metals less oxidisable than iron, it is typically
desirable to subject such articles to the step of annealing. Although the articles
are relatively difficult to oxidise, it is still nonetheless necessary to maintain
a reducing or non-oxidising atmosphere in the furnace used to perform the annealing
operation. It is known that in theory nitrogen may be used to form an atmosphere that
is inert for the purposes of annealing. Typically, the nitrogen may be supplied from
a source of nitrogen which has been separated from air by distillation at cryogenic
temperatures and need only contain parts per million of reactive impurities such as
oxygen. Such nitrogen can be used in a heat treatment shop as the atmosphere for a
range of different heat treatments. In recent years, it has been found that there
are certain economic advantages in producing the nitrogen on the site of its use by
non-cryogenic means rather than off-site by a cryogenic distillation process and then
transporting the nitrogen product to its site of use. There are two main ambient temperature
methods which may be used to separate nitrogen from air. The first is by pressure
swing adsorption which entails adsorbing oxygen from the air on an adsorbent to produce
a nitrogen product and then periodically regenerating the adsorbent by subjecting
it to a pressure lower than that at which adsorption takes place. The alternative
method is to separate air by means of semi-permeable membranes. Known semi-permeable
membranes suitable for the separation of air permit oxygen to diffuse through them
at a much more rapid rate than nitrogen with the result that the non-permeate gas
becomes enriched in nitrogen.
[0003] Such non-cryogenic methods are able to be used to produce a nitrogen product containing
in the order of 1% by volume of oxygen more cheaply than cryogenic methods may be
used to separate nitrogen from air, provided the cost of transporting the cryogenically
produced nitrogen to its site of use is taken into consideration. For many industrial
processes the fact that the non-cryogenically produced nitrogen contains in the order
of 1% of oxygen as an impurity is not a drawback. However, we have found that in the
annealing of metals less readily oxidisable than iron, such an oxygen concentration
is indeed a drawback. Although at first sight it may be thought that a suitable annealing
atmosphere may be produced by mixing hydrogen with the non-cryogenically produced
nitrogen, in for example the annealing of copper, which takes place at temperatures
of 400 to 800 C, the reaction between hydrogen and oxygen proceeds sufficiently slowly
at temperatures in at least the lower part of this temperature range for there to
be a substantial risk that oxidation of the copper will still take place notwithstanding
the addition of a stoichiometric excess of hydrogen to the atmosphere.
[0004] It is known to purify nitrogen containing about 1 % by volume of oxygen by subjecting
it to a process in which the oxygen is first catalytically reacted with hydrogen and
then the resulting water vapour is adsorbed by means of an adsorbent or getter. The
reliance on an adsorption step to purify the nitrogen requires the use of a kind of
apparatus in which there are two parallel adsorption stages, one of which is used
while the other is regenerated, so as to make possible continuous production of the
purified gas. The need for the adsorption stage adds considerably to the capital and
running cost of the apparatus and tends to eliminate the economic advantage that would
otherwise result from the production of nitrogen on-site by non-cryogenic means.
[0005] There is thus a need for a method and apparatus of annealing articles of metal less
oxidisable than iron which renders the use of non-cryogenically produced nitrogen
containing an appreciable quantity of oxygen impurity attractive from the economic
point of view.
[0006] According to the present invention there is provided a method of annealing an article
of a metal less oxidisable than iron, comprising the steps of subjecting the article
to an annealing temperature in a heat treatment furnace, separating nitrogen from
air at the site of the annealing furnace to produce a gas mixture containing at least
95% by volume of nitrogen and a minor proportion of oxygen impurity, catalytically
reacting the oxygen impurity with a stoichiometric excess of hydrogen to form water
vapour, and passing the resulting gas mixture comprising nitrogen, water vapour and
unreacted hydrogen into the furnace to create an annealing atmosphere.
[0007] Instead of using a stoichiometric excess of hydrogen the precise stoichiometric amount
of hydrogen as required by the reactions:
2H2 + 02 --> 2H20
may be employed. Accordingly the resulting gas mixture then contains no oxygen and
no hydrogen.
[0008] The invention also provides apparatus for annealing an article of a metal less oxidisable
than iron comprising an annealing furnace, means for separating a gas mixture comprising
at least 95% by volume of nitrogen and oxygen impurity from air, and a catalytic reactor
for catalytically reacting the oxygen impurity with a stoichiometric excess of hydrogen
to form a gas mixture comprising nitrogen, water vapour and unreacted hydrogen, wherein
said reactor has an outlet in communication with the annealing furnace so as to enable
a suitable annealing atmosphere to be created in the furnace.
[0009] The method and apparatus according to the invention are particularly suited for the
bright annealing of the metals less oxidisable than iron.
[0010] Preferably, the nitrogen product contains 0.5-3% by volume of oxygen upstream of
its catalytic reaction with hydrogen. In general only a small if any stoichiometric
excess of hydrogen is required. For example, in the bright annealing of copper at
a temperature in the order of 600 C, suitable annealing conditions can be maintained
provided that the ratio of the partial pressures of hydrogen to water vapour in the
annealing atmosphere does not fall below 1 x 10-
6.
[0011] The catalytic reaction preferably takes place over a platinum or palladium catalyst.
Alternatively, copper or nickel catalysts may be used. The catalyst is typically heated
by the reaction between hydrogen and oxygen to a temperature of up to 200 C.
[0012] The method and apparatus according to invention will now be described by way of example
with reference to the accompanying drawings, in which
Figure 1 is a schematic diagram of apparatus for the bright annealing of copper, and
Figure 2 is a schematic drawing illustrating apparatus according to the invention
including a continuous mesh belt furnace.
[0013] In Figure 1 of the drawings, there is shown a plant 2 for separating nitrogen from
air by pressure-swing adsorption. Suitable plants and apparatus for this purpose are
for example disclosed in Patent Specifications 2073043A and UK 2195097A. The resulting
nitrogen typically contains from 0.5 to 3% by volume of oxygen impurity. The nitrogen
stream is passed through a catalytic reactor 4 in which its oxygen impurity is reacted
with a small stoichiometric excess of hydrogen over a palladium or platinum catalyst
at a reaction temperature. The resulting gas mixture comprises nitrogen, hydrogen
and water vapour. It is admitted to the heat treatment furnace 6 which may be of a
batch or continuous kind in which an article made of copper or an alloy of copper
such as bronze, copper-nickel, or brass containing up to 15% by weight of zinc, is
annealed by immersion in an annealing atmosphere at a temperature of 400 ` -800` C
for a period of time typically in the order of 10 minutes to 2 hours. By maintaining
the ratio of the partial pressure of hydrogen to the partial pressure of water vapour
in the atmosphere and hence in the nitrogen supplied from the catalytic reactor 4
at a value not less than 1 x 10-
6 it is possible to maintain conditions in the atmosphere in which the copper is not
deoxidised. Therefore its bright surface is maintained during the annealing.
[0014] Referring to Figure 2 of the drawings, there is shown a conventional continuous mesh
belt furnace 10 having an inlet zone 12, 1 metre in length, a hot or heated zone 14,
5.67 metres in length, and a cooling zone 16, 6.86 metres in length. The furnace 10
is provided at its respective ends with baffles 18 or the like to impede the ingress
of air from outside the furnace into its interior. The hot zone 14 and the cooling
zone 16 have respectively inlets 20 and 22 for gas.
[0015] The inlets 20 and 22 are each alternatively able to be placed in communication for
source 24 of gas mixture comprising hydrogen, water vapour and nitrogen. The source
24 comprises a plant 26 for separating nitrogen from air by pressure swing adsorption,
and a catalytic reactor 28 for reacting oxygen impurity in the nitrogen with hydrogen.
A commercially available catalyst comprising palladium supported on alumina is used.
Typically, the catalyst is heated by the reaction between hydrogen and oxygen and
the gas mixture leaves the reactor 28 at a temperature in the range of 50 to 150 C.
[0016] In operation, a gas mixture comprising nitrogen, water vapour and hydrogen from the
catalytic reactor 28 is passed into the furnace 10 through either or both the inlets
20 and 22. The hot zone 14 is heated to a chosen temperature typically in the range
500 to 800° C. Copper work to be bright annealed is loaded onto the belt (not shown)
of the furnace and the belt is then advanced slowly through the furnace at a speed
such that the work typically has a residence time in the furnace of from 30 minutes
to 1 hour. As the work passes through the hot zone 14 so it is raised approximately
to the temperature of the hot zone 14. On leaving the hot zone 14 the work passes
into the cooling zone 16 in which it is cooled by contact with the relatively cold
atmosphere therein. Typically, the work is at a temperature between ambient and 50°
C when it leaves the furnace 10. By employing an atmosphere in accordance with the
invention, it can be ensured that bright annealed work leaves the furnace 10.
[0017] A number of experimental tests of the apparatus shown in Figure 2 were performed.
The results of the tests are set out in Tables 1 to 4 below.
[0018] Table 1 shows the results of comparative experiments in which various different proportions
of hydrogen were mixed with nitrogen from a PSA plant (0.5% oxygen impurity) and the
resulting mixture passed into the furnace without a catalytic reaction between hydrogen
and oxygen being performed. It was a feature of the furnace used that entry to the
hot zone was by way of a muffle made of an alloy with high nickel and chrome content
which had the property of acting as a getter for free oxygen. Accordingly, it was
found that substantially all the oxygen entering the furnace with the gas mixture
was removed therefrom. It was therefore possible to obtain bright work (at 750. C)
even when the oxygen level was nominally in excess of the stoichiometric requirement
for reaction with hydrogen. Results are given in Table 1 for the oxygen concentration,
hydrogen concentration and dew point in both the hot zone 14 and the cooling zone
16 of the furnace 10 at the different hydrogen levels.
[0019] The results set out in Table 2 relate to a set of experiments similar to those of
Table 1 save that the mixture of nitrogen, oxygen and hydrogen was reacted in the
catalytic reactor 28 upstream of being admitted to the hot zone of the furnace through
the inlet 20.
[0020] The Experiments illustrated in Table 3 and 4 are respectively comparable to those
set out in Tables 1 and 2 with the exception that the gas mixture is not introduced
directly into the hot zone 14 through the inlet 20. Rather, it is introduced directly
into the cooling zone 16 through the inlet 22. Table 3 shows experiments in which
the gas mixture by-passed the catalytic reactor 28, whereas Table 4 relates to experiments
in which the catalytic reactor was used. The low dew points obtained in the experiments
illustrated by Table 3 indicate that when the gas mixture is supplied directly to
the cooling zone, a failure to react the oxygen with at least a stoichiometric quantity
of hydrogen in the catalytic reactor 28 will tend to result in work that is not bright
even if the hot zone is ooerated at a temperature as high as 750 C.
NOTE
[0022] Oxygen concentrations were measured using an oxygen probe. The temperature of the
gas from the hot zone at the sampling point was 750° C: the temperature of the gas
from the cooling zone at the sampling point was 200°C. Most results are shown in Millivolts
(mV). The actual oxygen concentration can be calculated using the formula
E = 0.0215.T. loge (20.95/% 02)
where
E is the oxygen probe reading in mV
T is the temperature in Kelvin at the oxygen probe location.
%O2 is the concentration of oxygen expressed as a percentage by volume.
1. A method of annealing an article of a metal less oxidisable than iron, comprising
the steps of subjecting the article to an annealing temperature in a heat treatment
furnace, separating nitrogen from air at the site of the annealing furnace to produce
a gas mixture containing at least 95% by volume of nitrogen and a minor proportion
of oxygen impurity, catalytically reacting the oxygen impurity with a stoichiometric
excess of hydrogen to form water vapour, and passing the resulting gas mixture comprising
nitrogen, water vapour and unreacted hydrogen into the furnace to create an annealing
atmosphere.
2. A method of annealing an article of a metal less oxidisable than iron, comprising
the steps of subjecting the article to an annealing temperature in a heat treatment
furnace, separating nitrogen from air at the site of the annealing furnace to produce
a gas mixture containing at least 95% by volume of nitrogen and a minor proportion
of oxygen impurity, catalytically reacting the oxygen impurity with a stoichiometric
quantity of hydrogen to form water vapour, and passing the resulting gas mixture comprising
nitrogen and water vapour into the furnace to create an annealing atmosphere.
3. A method according to Claim 1 or Claim 2, in which the nitrogen product contains
0.5-3% by volume of oxygen upstream of its catalytic reaction with hydrogen.
4. A method according to any one of the preceding claims, in which the catalytic reaction
takes place over a platinum or palladium catalyst.
5. A method according to any one of the preceding claims, in which the metal is cobalt,
nickel, lead, copper, palladium, silver or gold, or an alloy of at least one of such
metals, or as alloy of mercury.
6. A method according to any one of the preceding claims, in which the metal is bright
annealed.
7. A method according to any one of the preceding claims, in which the resulting gas
mixture is introduced directly into the cooling zone of a continuous furnace.
8. Apparatus for annealing an article of a metal less oxidisable than iron comprising
an annealing furnace, means for separating a gas mixture comprising at least 95% by
volume of nitrogen and a minor proportion of oxygen impurity from air, and a catalytic
reactor for catalytically reacting the oxygen impurity with a stoichiometric excess
of hydrogen to form a gas mixture comprising nitrogen, water vapour and unreacted
hydrogen, wherein said reactor has an outlet in communication with the annealing furnace
so as to enable a suitable annealing atmosphere to be created in the furnace.
9. Apparatus according to claim 8, in which the catalytic reactor includes a platinum
or palladium catalyst.