[0001] Graphite fibres are generally different from carbon fibres in respect of carbon content
(purity), structure and physical characteristics. Graphite fibres are preferable to
carbon fibres for use in sports equipment such as fishing rods and golf club shafts
which require high modulus, for use in electric components such as heaters which require
high purity and low resistivity, and for use in the aerospace industry, where parts
for aircraft, rockets etc., may have to have high oxidation resistivity and be made
to high precision. However, graphite fibres cost much more than carbon fibres and
this high cost is largely a result of difficulties in manufacturing processability
and productivity. An inert atmosphere is required for production of graphite fibres,
and a higher temperature is used than for carbon fibres.
[0002] Efforts have been made to increase productivity in manufacturing graphite fibres.
For example, it has been proposed to increase the temperature gradient and to shorten
the time in graphitizing furnace. However, this produces increased amounts of fuzz
on the surface of the graphite fibres and occasional breakage of the fibre strands.
[0003] Also, these modifications tend to reduce the tensile strength of the fibres. Further,
since the temperature of the inert atmosphere must be higher than that used for manufacturing
carbon fibres the wear on the graphitizing furnace, particularly on its heating pipes,
is considerably greater. As a result of such wear due to exceedingly high temperatures,
deviations from the desired temperature profile tend to increase and the furnace tube
must be changed frequently. This seriously interferes with production and processability,
and also consumes large amounts of energy, labour and materials.
[0004] According to the present invention there is provided a process for the manufacture
of graphite fibre by graphitizing precursor fibre characterised in that the precursor
fibre or fibres pass successively through separately controllable first and second
heating zones, both containing an inert atmosphere, the temperature at the hottest
point in the said first heating zone being in the range of about 1500°C to about 2l00
oC, and the temperature at the hottest part in the said second heating zone being at
least about 2100°C.
[0005] By use of the present invention it is possible to obtain a stable method of manufacturing
high grade and high quality graphite fibres, particularly graphite fibres which have
a minimum of surface fuzz. The process may use a shorter heating zone than is usual
in conventional processes. Additionally, it is possible to provide a manufacturing
process in which the life of parts is lengthened, and their replacement is easier,
thereby saving energy, materials and labour.
[0006] The term "graphite fibre" as used herein is intended to mean a fibre which is obtained
by heating a graphitizable precursor fibre in an inert atmosphere at a temperatue
of about 2100°C, or more and which fibre contains about 95% or more by weight of carbon.
The term "graphitizable precursor fibre" or "precursor fibre" is intended to mean
a fibre which has sufficient structural integrity to maintain its fibrous character
and which can be converted to a graphite fibre when heated in an inert atmosphere
at a temperature of about 2100
oC or more. A typical example of a precursor fibre is an oxidized fibre obtained by
heating an acrylic fibre, a cellulosic fibre (rayon), a polyvinylalcohol fibre or
a pitch fibre in an oxidizing atmosphere at a temperature of about 200°C to 400°C.
Another typical example is a carbon fibre obtained by heating the said oxidized fibre
in an inert atmosphere at a temperature above about 400°C. When using the process
of the present invention it is preferable to use a precursor fibre obtained from an
acrylic fibre comprising about 95 mol % minimum of acrylonitrile (AN) and up to about
5 mol % of one or more ethylene-type vinyl compounds which are copolymerizable with
acrylonitrile.
[0007] The maximum temperature in the first heating zone is preferably in the range of 1700°Cto
1900°C. The second heating zone preferably has a maximum temperature in the range
of 2100°C to 3500°C, more preferably in the range of 2300°C to 2700°C.
[0008] It has been discovered that if the front and rear heating zones are operated at heating
temperatures outside the ranges from 1500°C to 2100°C and 2100°C to 3500°C, respectively,
it is difficult to obtain high quality graphite fibre. The quality of the fibre produced
is influenced by such things as the type of precursor fibre, whether it was pretreated
or not, and the temperature profile of the heating zone; in some instances it is especially
sensitive to the maximum temperature of the first heating zone and is reduced if this
exceeds about 2100°C. In particular, the fibres tend to develop excessive surface
fuzz and tend to break easily.
[0009] The rate of heating of the precursor fibre as it passes through the heating zones
is preferably within the range of 300°C/min to 2000°C/min in the first heating zone,
more preferably within the range of 500°C/min to 1500°C/min, and preferably within
the range of 2000°C/min to 10,000°C/min in the second heating zone.
[0010] The treatment time of the precursor fibres in the first heating zone, which is defined
as the time during which the fibres are in the zone at a temperature above 1000°C.
is preferably within the range of 10 seconds to 10 minutes, more preferably 30 seconds
to 3 minutes.
[0011] An embodiment of the present invention will now be described by way of example with
reference to the drawings, in which:
Fig. 1 is a view in longitudinal section of graphitizing apparatus for carrying out
the process of this invention;
Figs. 2 and 3 respectively show typical examples of temperature profiles in the furnace
tubes used in the respective heating zones.
[0012] Referring to Fig. 1, the separate first and second heating zones (furnaces) have
respectively furnace tubes (2,3) to which heat is applied in a conventional way. The
furnace tubes (2,3) are surrounded with insulation (4,5). An inert gas such as nitrogen
is supplied to the furnaces (I,II) through pipes (6), and the gas is removed from
the furnaces by pipes (7). At each end of each furnace there are furnace seals (8),
supplied with inert gas through supply pipes (9).
[0013] As shown in Fig. 1, the precursor fibre (1) is first conducted through the seal (-8)
into the furnace tube (2) of the furnace (1) which provides the first heating zone.
The temperature profile inside this furnace tube (2) is controlled, to produce a profile
as shown in Fig. 2. This is done by locally controlling the heat input at selected
spots along the tube (2), in a conventional way. When the precursor fibre is a carbon
fibre, it is treated in this furnace until its weight is reduced to about 93% to 95%
of its previous weight, and then it is conducted into the furnace tube (3) of the
furnace (II) which provides the second heating zone. There the fibre is heated again,
and is converted into a graphite fibre. Fig. 3 shows a typical temperature profile
of the furnace tube (3) of the second heating zone, the maximum temperature of which
is set at about 2500°C in this case.
[0014] By use of the present invention, a more efficient and therefore more profitable process
for the manufacture of graphite fibres is possible. These advantages can be realised
for the following reasons:
(a) The heating zone is divided into two independently controlled zones, giving increased
flexibility with the rate of heating the fibre. There is also better control of the
temperature profile within the furnace;
(b) The weight loss of the precursor fibre during initial heating up to 1500°C is
usually large. It has been found that the use of a high rate of heating in the stage
up to 1500°C tends to damage the precursor fibre. In the conventional, single heating
zone system, the overall rate of heating must be so low that it restricts overall
productivity. By use of the present, double heating zone system, it is possible to
select optimum rates of heating for the first and second heating zones independently
of each other. This allows manufacture of high quality graphite fibres with increased
productivity;
(c) With the process of the present invention, it is possible to reduce the overall
length of the heating zone by dividing it, and the maintenance and custody of the
furnace can thereby be made easier. The life of a furnace tube in the second furnace
is much shorter than that of one in the first furnace, because of the higher temperature
at which it operates. However, clearly the tube in the first furnace need not be replaced
merely because the tube in the second furnace has to be, and also the tube in the
second furnace, being relatively short compared with the tube in a single-heating
zone furnace, is easier to handle. Thus, costs of time, labour, and materials can
be reduced. Surprisingly the energy consumption can also be reduced. This is because
it has been found possible to string up the fibres without lowering the temperatue
of the furnace.
EXAMPLES.
[0015] Carbon fibres were produced from acrylic fibres and carbonized in an inert atmosphere,
the maximum temperature of which was 1100°C. They were taken from creels and heated
to produce graphite fibres using separate furnaces as shown in Fig. 1. The conditions
were varied, there being 3 conditions within the scope of the invention (Examples
1-3) and four conditions outside the scope of the invention (Comparative Examples
1-4). The conditions are shown in Table 1.

The resulting data are shown in Table 2. Moreover, the usual temperatures, the periods
of time between changes of furnace tubes and the number of days required to change
them, with respect to both first and second furnaces, are shown in Table 3. Some of
the properties of the fibres made in these examples are shown in Table 2.
[0016] Table 3 gives an indication of the lifetime of the furnace tubes, at different operating
temperatures, and the time taken to change them.

1. A process for the manufacture of graphite fibre by graphitizing precursor fibre
characterised in that the' precursor fibre or fibres pass successively through separately
controllable first and second heating zones, both containing an inert atmosphere,
the temperature at the hottest point in the said first heating zone being in the range
of about 1500°C to about 2100°C, and the temperature at the hottest part in the said
second heating zone being at least about 2100°C.
2. A process according to claim 1 in which the two heating zones are constituted by
separate furnace tubes separately heated and furnished with inert atmosphere.
3. A process according to claim 1 or claim 2 in which the said temperature at the
hottest point in the first heating zone is in the range of from 1700°C to 1900°C.
4. A process according to any one of claims 1 to 3 in which the said temperature at
the hottest point in the second heating zone is in the range of 2100°C to 3500°C.
5. A process according to claim 4 in which the said temperature at the hottest point
in the second heating zone is in the range of from 2300°C to 2700°C.
6. A process according to any one of the preceding claims in which the average rate
of heating of fibre in the first heating zone is in the range of from 300°C/min to
2000°C/min.
7. A process according to any one of the preceding claims in which the average rate
of heating of fibre in the second heating zone is in the range of from 2000°C/min
to 10,000°C/min.
8. A process according to any one of the preceding claims in which the precursor fibre
is a converted polyacrylonitrile fibre.
9. A process according to claim 8 in which the precursor fibre is a carbon fibre obtained
from an acrylic fibre comprising at least 95 mol % of acrylonitrile and up to 5 mol
% of one or more ethylene-type vinyl compounds copolymerizable with acrylonitrile
by heating and oxidizing the said acrylic fibre in an oxidizing atmosphere at a temperature
in the range of about 200°C to about 400°C, and then heating the oxidized fibre so
formed in an inert atmosphere at a temperature of from 400°C to 1500°C.
10. A process according to claim 8 in which the precursor fibre is an oxidized fibre
obtained from an acrylic fibre comprising at least 95 mol % of acrylonitrile and up
to 5 mol % of one or more ethylene-type vinyl compounds copolymerizable with acrylonitrile,
by heating and oxidizing the said acrylic fibre in an oxidizing atmosphere at a temperature
of from about 200°C to about 400°C.