[0001] This invention relates to carbon fibers sized with a sizing agent.
[0002] Because of their excellent strength, modulus and heat resistance, carbon fibers are
now utilized in a variety of applications. Carbon fibers, however, pose a problem
because they are apt to be damaged during processing which includes repeated bending
and repeated frictional contact with, for example, guide rollers, thereby causing
cleavage of filaments and fluff of the fibers. In the preparation of fiber-reinforced
composite material, the fluff of carbon fibers impede the compatibility thereof with
a matrix resin so that the composite material fails to exhibit satisfactory mechanical
properties. To cope with this problem, a method is proposed for treating carbon fibers
with a sizing agent.
[0003] Known sizing agents include organic solutions or aqueous emulsions containing binder
resins such as vinyl acetate polymers, acrylic polymers, polyurethanes, epoxy resins
and polystyrenes. These conventional sizing agents, however, are not entirely satisfactory
with respect to anti-spreading or fluff-preventing property, especially when they
are used for the treatment of petroleum pitch-derived carbon fibers.
[0004] It is an object of the present invention to provide petroleum pitch-derived, sized
carbon fibers which are excellent in anti-spreading property, lubricity and flexibility
and, therefore, are free of occurrence of fluff and filament cleavage during processing
such as weaving.
[0005] In accordance with the present invention there is provided petroleum pitch-derived
carbon fibers coated with a sizing agent comprising the following ingredients (a)-(c):
(a) an epoxy resin having a number average molecular weight of 550-1600 wherein the
content of epoxy resin components which are equivalent to polystyrenes having a molecular
weight of 10000 or more with respect to retention time in gel permeation chromatography
is less than 5 mol %,
(b) at least one ether compound of the general formula:
X - O - y
wherein X represents a polyoxyalkylene group and Y represents an aromatic group; and
(c) an ester compound selected from the group consisting of unsaturated fatty acid
esters of an aliphatic monohydric alcohol and aliphatic monocarboxylic acid esters
of an unsaturated aliphatic monohydric alcohol, wherein the amounts of ingrdients
(a)-(c) are 55-84 %, 15-35 % and 1-25 %, respectively, based on the total weight of
ingredients (a)-(c).
[0006] In another aspect, the present invention provides a product obtained by a method
comprising the steps of:
providing carbon fibers derived from petroleum pitch;
contacting said carbon fibers with an aqueous emulsion containing the following ingredients
(a)-(c):
(a) an epoxy resin having a number average molecular weight of 550-1600 wherein the
content of epoxy resin components which are equivalent to polystyrenes having a molecular
weight of 10000 or more with respect to retention time in gel permeation chromatography
is less than 5 mol %,
(b) at least one ether compound of the general formula:
X - O - Y
wherein X represents a polyoxyalkylene group and Y represents an aromatic group; and
(c) an ester compound selected from the group consisting of unsaturated fatty acid
esters of an aliphatic monohydric alcohol and aliphatic monocarboxylic acid esters
of an unsaturated aliphatic monohydric alcohol, wherein the amounts of ingrdients
(a)-(c) are 55-84 %, 15-35 % and 1-25 %, respectively, based on the total weight of
ingredients (a)-(c), thereby coating said carbon fibers with said aqueous emulsion;
and
drying said aqueous emulsion coating.
The present invention will now be described in detail below.
[0007] The present invention is characterized in that petroleum pitch-derived carbon fibers
are treated and coated with a specific sizing agent in the form of an aqueous emulsion
including ingredients (a)-(c). These ingredients will be described below.
Ingredient (a):
[0008] is an epoxy resin having a number average molecular weight of 550-1600, preferably
600-900. When the number average molecular weight of the epoxy resin is below 550,
the resulting sized fibers are sticky and high in frictional resistance. Further,
the anti-spreading property becomes insufficient. As a result, the fibers tend to
fluff upon running contact with guide rollers. This is particularly outstanding when
the fibers are pitch-derived carbon fibers having a high elastic modulus of more than
40 ton/mm². When the number average molecular weight exceeds 1600, on the other hand,
the emulsion becomes so unstable that sizing treatment cannot be efficiently performed.
[0009] It is important that the content of epoxy resin components of ingredient (a) which
are equivalent to polystyrenes having a molecular weight of 10000 or more with respect
to ellution characteristics (retention time), namely with respect to molecular weight,
in gel permeation chromatography is less than 5 mol %, since otherwise the emulsion
is unstable and becomes heterogeneous so that it is impossible to effect the sizing
treatment.
[0010] Any epoxy resin may be used as long as the above requirements are satisified. Thus,
bisphenol type epoxy resins, phenol novolak epoxy resins, cresol novolak epoxy resins
and diaminodiphenylmethane epoxy reins may be used as the epoxy resin of ingredient
(a). Suitable epoxy resins may be obtained by blending the following epoxy resins
and their homologues:

For example, a blend of EPIKOTE 828 and EPIKOTE 1001 (weight ratio of EPIKOTE 828/EPIKOTE
1001 of 46:54 to 0:100), a blend of EPIKOTE 828 and EPIKOTE 1002 (weight ratio of
EPIKOTE 828/EPIKOTE 1002 of 47:53 to 0:100) and a blend of EPIKOTE 828 and EPIKOTE
1004 (weight ratio of EPIKOTE 828/EPIKOTE 1004 of 59:41 to 25:75) are suitably used
as ingredient (a).
Ingredient (b):
[0011] is at least one ether compound of the general formula:
X - O - Y
wherein X represents a polyoxyalkylene group and Y represents an aromatic group. Examples
of the polyoxyalkylene group X include a polyoxyethylene, a polyoxypropylene or a
copolymer of ethylene oxide and propylene oxide. Examples of the aromatic group Y
include:

where Z is an alkylene
group such as methylene, ethylene, propylene or isopropylene, an alkenylene group
such as vinylene, R¹ is hydrogen a hydroxyl group or an alkyl group and m is an integer
of 1-5;

where R² is an alkyl group and n is an integer of 1-5; and
a polycondensed ring aromatic group such as naphthyl or alkylnaphthyl.
[0012] Thus, the ingredient (b) is preferably one or more of the following ether compounds:
(b-1): an ether of the formula:

where X, 2, R¹ and m are as defined above;
(b-2): an ether of the formula:

where X, R² and n are as defined above; or
(b-3): an ether of a polyoxyalkylene and a polycondensed ring aromatic alcohol.
[0013] Examples of ethers (b-1) include polyoxyalkylene ethers of styrenated phenols such
as polyoxyalkylene monostyrylphenyl ether, polyoxyalkylene distyrylphenyl ether, polyoxyalkylene
tristyrylphenyl ether and polyoxyalkylene polystyrylphenyl ether; polyoxyalkylene
ethers of benzylated phenols such as polyoxyalkylene monobenzylphenyl ether, polyoxyalkylene
dibenzylphenyl ether, polyoxyalkylene tribenzylphenyl ether, polyoxyalkylene tetrabenzylphenyl
ether and polyoxyalkylene pentabenzylphenyl ether; and polyoxyalkylene ethers of bisphenols
such as bispenol A polyoxyalkyl ether and bisphenol F polyoxyalkyl ether.
[0014] Examples of ethers (b-2) include polyoxyalkylene ethylphenyl ether, polyoxyalkylene
propylphenyl ether, polyoxyalkylene butylphenyl ether, polyoxyalkylene pentylphenyl
ether, polyoxyalkylene hexylphenyl ether, polyoxyalkylene heptylphenyl ether, polyoxyalkylene
octylphenyl ether, polyoxyalkylene nonylphenyl ether, polyoxyalkylene decylphenyl
ether and polyoxyalkylene dodecylphenyl ether.
[0015] It is preferred that a mixture of an ether (b-I) with an ether (b-2) or a mixture
of an ether (b-2) with an ether (b-3) be used as ingredient (b).
Ingredient (c):
[0016] is an ester compound selected from the group consisting of unsaturated fatty acid
esters of an aliphatic monohydric alcohol and aliphatic monocarboxylic acid esters
of an unsaturated aliphatic monohydric alcohol.
[0017] Examples of ingredient (c) include octyl oleate, lauryl oleate, stearyl oleate, isotridecyl
oleate, oleyl oleate, oleyl stearate, oleyl laurate, oleyl isostearate, oleyl palmitate
and oleyl octalate.
[0018] It is necessary that the amounts of ingrdients (a)-(c) should be 55-84 %, 15-35 %
and 1-25 %, respectively, based on the total weight of ingredients (a)-(c). Preferred
amounts of ingrdients (a)-(c) are 60-75 %, 20-30 % and 5-10 %, respectively, based
on the total weight of ingredients (a)-(c).
[0019] An amount of ingredient (a) below 55 % by weight causes deterioration of anti-spreading
property of the carbon fibers so that the fibers tend to fluff when subjected to repeated
frictional forces. When the amount of ingredient (a) exceeds 84 % by weight, the emulsion
of the sizing agent becomes unstable and homogeneous elulsion cannot be obtained.
This also applies to the case where the amount of ingredient (b) is below 15 % by
weight. Too large an amount of ingredient (b) in excess of 35 % by weight, on the
other hand, is disadvantageous because the anti-spreading property of the carbon fibers
is deteriorated so that the fibers tend to fluff when subjected to repeated frictional
forces. When the amount of ingredient (c) is below 1 % by weight, the sized fibers
become poor in lubricity and tend to fluff when subjected to repeated frinctional
forces. Too large an amount of ingredient (c) in excess of 25 % by weight adversely
affects the adhesion of the fibers to a matrix resin of a composite material.
[0020] The above ingredients (a)-(c) are emulsified in water to obtain a sizing agent in
the form of an emulsion. The total concentration of ingredients (a)-(c) in the emulsion
is generally 0.2-10 % by weight. The emulsion is used for the sizing treatment of
petroleum pitch-derived carbon fibers.
[0021] Petroleum pitch is a carbonaceous pitch obtained from heavy hydrocarbon oils such
as atmospheric pressure distillation residues, vacuum residues, vacuum distillation
heavy distillates, catalytic cracking heavy distillates (e.g. recycle oils), catalytic
cracking residual oils (including tar), steam cracking heavy distillates, steam cracking
residual oils (including tar), and other heavy oils obtained in petroleum refining
processes. If desired, these heavy hydrocarbon oils may be subjected to filtration,
solvent extraction or other pretreatment before conversion into pitch. The petroleum-derived
pitch may be used in conjunction with a coal tar pitch obtained from coal-derived
heavy oils (including liquified coal oils) or coal tar, or with a synthetic pitch
obtained from aromatic compounds or polynuclear condensed compounds. Carbon fibers
may be obtained from the above pitch by any known manner.
[0022] The petroleum pitch-derived carbon fibers, which may be in the form of a tow, are
sized with the above-described emulsified sizing agent by any known method such as
a roller sizing method, a roller immersion method or a spray coating method so that
the sizing agent is coated over the fibers in an amount of 0.1-5.0 % by weight, preferably
0.5-3.0 % by weight (on dry basis) based on the weight of the fibers.
[0023] The following examples will further illustrate the present invention.
Example 1
[0024] A first glycidyl ether of bisphenol A (EPIKOTE 828 manufactured by Yuka-Shell Epoxy
Inc.) was mixed with a second glycidyl ether of bisphenol A (EPIKOTE 1001 manufactured
by Yuka-Shell Epoxy Inc.) to obtain Ingredient (a) having a number average molecular
weight of 670. GPC analysis revealed that Ingredient (a) had a content of components
having a molecular weight (PS equivalent molecular weight) of 10,000 of less than
0.5 mole %. The GPC analysis was conducted by Gel Permeation Chromatogram GPC LC-6A
(manufactured by Shimadzu Ltd.) equipped with three 30 cm columns (HGS-40H, 20H and
15H) using tetrahydrofuran as an elution solvent.
[0025] Into pure water were emulsified 75 parts by weight of Ingredient (a), 14 parts of
Ingredient (b-1 )which was polyoxyalkylene(3 mol, PO/EO molar ratio: 1/3)polyoxyethylene(20
mol) tristyryl phenyl ether (PO represents polyoxypropylene and EO represents polyoxyethylene),
6 parts of Ingredient (b-2) which was polyoxyethylene(8 mol) nonylphenyl ether and
5 parts of Ingredient (c) which was lauryl oleate to obtain an aqueous emulsion having
a total concentration of Ingredients (a)-(c) of 2 % by weight. This emulsion was found
to be stable and to remain homogeneous after being allowed to stand for 5 hours.
[0026] Carbon fibers (derived from petroleum pitch, modulus: 50 ton/mm², filament number:
3000) in the form of a thread were subjected to a sizing treatment using the thus
obtained aqueous emulsion as a sizing agent. Thus, the fibers were immersed in the
aqueous emulsion and squeezed so that the amount of the emulsion contained in the
fibers was adjusted to 1 g per 1 g of the fibers. The thus treated fibers were then
dried with a hot wind blow at 110 °C.
[0027] The treated carbon fibers were then tested for running friction force to give the
following results:
Fiber-Fiber (F/F) frictional force: 105 g
Fiber-Metal (F/M) frictional force: 220 g
The frictional force was measured as follows:
F/F Frictional Force:
[0028] A running friction force tester composed of two tension meters, guide rollers and
a thread feeder is used. An increase in tension due to the friction between the threads
is measured with the tension meters. The twist angle is 540°, the crossing angle is
30° and the running speed is 2.0 m/minute. The difference in frictional force between
the two tension meters represents the F/F frinctional force. The initial load applied
is 20 g.
F/M Frictional Force:
[0029] A running friction force tester composed of two tension meters, guide rollers, a
metal friction bar and a thread feeder is used. An increase in tension due to the
friction between the running thread and the bar is measured with the tension meters.
The difference in frictional force between the two tension meters represents the F/M
frictional force.
[0030] The carbon fibers treated with the sizing agent were found to exhibit good anti-spreading
tendency. As expected from the low F/F and F/M frictional forces, the fibers scarecely
fluffed even when they are rubbed with each other or with a metal bar.
[0031] The sized fibers were also tested for their adhesion to epoxy resin. Thus, a carbon
fiber-reinforced plate (Vf: 60%) in which the carbon fibers were uniaxially oriented
within a matrix of a hardened epoxy resin was prepared. The matrix resin was formed
by hardening a composition containing 100 parts by weight of an epoxy resin (EPIKOTE
828 manufactured by Yuka-Shell Epoxy Inc.), 85 parts by weight of an acid anhydride
curing agent (HN-5500 manufactured by Hitachi Chemical Co., Ltd.) and 1 part by weight
of a curing promoter (ethylmethylimidazole) at 120 °C for 1 hour followed by post
curing at 180 °C for 1 hour. The thus prepared plate was subjected to a short beam
three-point bending (length/height: 4) test to measure the interlaminar shear strength
(ILSS). The interlaminar shear strength was 7.8 kg/mm².
Examples 2-6
[0032] Example 1 was repeated in the same manner as described except that the kinds and/or
amounts of Ingredients (a)-(c) were varied as indicated in Table 1 below. The results
are summarized in Table 2 together with those of Example 1.
Comparative Examples 1-5
[0033] Example 1 was repeated in the same manner as described except that the kinds and/or
amounts of Ingredients (a)-(c) were varied as indicated in Table 1 below. The results
are summarized in Table 2 together with those of Example 1.
Comparative Examples 6-9
[0035] Emulsions were prepared in the same manner as described in Example 1 using Ingredients
(a)-(c) indicated in Table 3. After 5 hours from the preparation, the emulsions were
found to form precipitates and become non-uniform. Stable emulsions were not obtained.

1. Petroleum pitch-derived carbon fibers coated with a sizing agent comprising the following
ingredients (a)-(c):
(a) an epoxy resin having a number average molecular weight of 550-1600 wherein the
content of epoxy resin components which are equivalent to polystyrenes having a molecular
weight of 10000 or more with respect to retention time in gel permeation chromatography
is less than 5 mol %,
(b) at least one ether compound of the general formula:
X - O - Y
wherein X represents a polyoxyalkylene group and Y represents an aromatic group; and
(c) an ester compound selected from the group consisting of unsaturated fatty acid
esters of an aliphatic monohydric alcohol and aliphatic monocarboxylic acid esters
of an unsaturated aliphatic monohydric alcohol, wherein the amounts of ingrdients
(a)-(c) are 55-84 %, 15-35 % and 1-25 %, respectively, based on the total weight of
ingredients (a)-(c).
2. Carbon fibers according to claim 1, wherein ingredient (b) is at least one ether compound
selected from the group consisting of (b-1), (b-2) and (b-3),
(b-1) being an ether of the formula:

where X is as defined above, Z is an alkylene group or an alkenylene group, R¹ is
hydrogen, a hydroxyl group or an alkyl group and m is an integer of 1-5,
(b-2) being an ether of the formula:

where X is as defined above, R² is an alkyl group and n is an integer of 1-5, and
(b-3) being an ether of a polyoxyalkylene and a polycondensed ring aromatic alcohol.
3. Carbon fibers according to claim 2, wherein ingredient (b) is a mixture of an ether
compound (b-1) with an ether compound (b-2) or a mixture of an ether compound (b-2)
with an ether compound (b-3).
4. A product obtained by a method comprising the steps of:
providing carbon fibers derived from petroleum pitch;
contacting said carbon fibers with an aqueous emulsion
containing the following ingredients (a)-(c):
(a) an epoxy resin having a number average molecular weight of 550-1600 wherein the
content of epoxy resin components which are equivalent to polystyrenes having a molecular
weight of 10000 or more with respect to retention time in gel permeation chromatography
is less than 5 mol %,
(b) at least one ether compound of the general formula:
X - O - Y
wherein X represents a polyoxyalkylene group and Y represents an aromatic group; and
(c) an ester compound selected from the group consisting of unsaturated fatty acid
esters of an aliphatic monohydric alcohol and aliphatic monocarboxylic acid esters
of an unsaturated aliphatic monohydric alcohol, wherein the amounts of ingrdients
(a)-(c) are 55-84 %, 15-35 % and 1-25 %, respectively, based on the total weight of
ingredients (a)-(c), thereby coating said carbon fibers with said aqueous emulsion;
and
drying said aqueous emulsion coating.
5. A product according to claim 4, wherein ingredient (b) is at least one ether compound
selected from the group consisting of (b-1), (b-2) and (b-3),
(b-I) being an ether of the formula:

where X is as defined above, Z is an alkylene group or an alkenylene group, R¹ is
hydrogen, a hydroxyl group or an alkyl group and m is an integer of 1-5,
(b-2) being an ether of the formula:

where X is as defined above, R² is an alkyl group and n is an integer of 1-5, and
(b-3) being an ether of a polyoxyalkylene and a polycondensed ring aromatic alcohol.
6. A product according to claim 5, wherein ingredient (b) is a mixture of an ether compound
(b-1) with an ether compound (b-2) or a mixture of an ether compound (b-2) with an
ether compound (b-3).