JPH0148313B2 - - Google Patents

Description

[Detailed description of the invention]

The present invention relates to a method for producing pitch, which has excellent performance as a raw material for producing carbon fibers. Currently, carbon fiber is mainly manufactured using polyacrylonitrile as a raw material. However, when polyacrylonitrile is used as a raw material, there are disadvantages in that the raw material is expensive, the original fibrous shape is easily destroyed during heating and carbonization, and the carbonization yield is also poor. In recent years, focusing on this point, many methods have been reported for producing carbon fibers using pitch as a raw material.
When pitch is used as a raw material, it is expected that carbon fibers can be produced at low cost because the raw material is inexpensive and the carbonization yield is usually as high as 85 to 95%. However, compared to polyacrylonitrile-based carbon fiber, carbon fiber obtained from pitch is
Although it has a high elastic modulus, it has a problem of poor strength. Therefore, if this problem could be solved and the modulus of elasticity could be further improved, it would be possible to produce carbon fibers with high strength and high modulus at low cost from pitch. Recently, commercially available petroleum pits have been heat-treated to obtain pitches containing optically anisotropic liquid crystals called mesophases, and pitches containing this mesophases have been converted into precursor pits (hereinafter referred to as molten). Carbon fibers with improved elastic modulus and strength can be obtained by melt-spinning this precursor pitch, making it infusible, and then carbonizing or graphitizing it. It was reported (Japanese Unexamined Patent Publication No. 19127-1983). However, whether or not a pitch can form a liquid crystal is determined by various factors, and the physical properties such as the structure, softening point, and viscosity of the liquid crystal greatly depend on the raw material pitch. Said Japanese Unexamined Patent Application Publication No. 1973-
No. 19127 relates to a method for preparing pitch containing mesophase (hereinafter abbreviated as mesophase pitch), but does not mention anything about the raw material pitch for forming high quality mesophase pitch. As mentioned above, a high-quality mesophase pitch largely depends on the raw material pitch, and if an optimal raw material pitch can be found, it will be possible to produce carbon fibers with even better elastic modulus and strength. Therefore, finding this optimal raw material pitch is an important challenge in this technical field. For example, coal tar pitch contains substances that are insoluble and infusible in carbon black quinoline, and these not only cause non-uniformity of the precursor pitch and deteriorate spinnability, but also reduce the strength and strength of carbon fibers. Adversely affects elastic modulus. On the other hand, many commercially available petroleum pitches and other synthetic pitches contain almost no substances that are insoluble and infusible in quinoline. Insoluble high molecular weight components are produced. In other words, when these pitches are heat-treated, thermal decomposition and polycondensation reactions occur simultaneously, and the low molecular weight components gradually become high molecular weight.
It becomes a high molecular weight component that is insoluble in quinoline, and at the same time, the high molecular weight component further increases in molecular weight. Along with this, the softening point of pitch also increases. If this quinoline insoluble matter is similar to the carbon black-like substance in coal tar, it will have an adverse effect on the steps after spinning as described above. Furthermore, even if the substance is different from the carbon black-like substance mentioned above,
The presence of a large amount of quinoline insolubles and a high softening point have an adverse effect on the melt spinning stage. In other words, in order to melt-spun a precursor pitch, it is necessary to raise the spinning temperature until the precursor pitch has a viscosity that allows spinning, and if the softening point of the precursor pitch is too high, the spinning temperature may As a result, the molecular weight of the insoluble portion of quinoline becomes even higher, and the pitch is thermally decomposed and light gas is generated, making it impossible to form a uniform precursor pitch and making it difficult to spin. It becomes virtually impossible. Thus, the precursor pitch must have a relatively low softening point and a suitable viscosity for spinning. Furthermore, it must not substantially contain volatile components during spinning or carbonization. For this reason, precursor pitch for carbon fiber production is prepared by removing the generated quinoline insoluble matter by means such as pressurization and solvent separation (Japanese Patent Application Laid-Open No. 47-9804, 50 −142820,
55-1342, 55-5954). however,
When these means are used, the processing equipment becomes complicated and the processing cost increases, which is not preferable from an economic point of view. It would be most preferable if a pitch having excellent performance could be used as the raw material pitch to prevent the formation of high molecular weight components that would become quinoline-insoluble components during the heating step of mesophase formation. The present inventors have completed the present invention as a result of intensive research into these problems. That is, the present inventors suppressed the formation of high molecular weight components at the stage of preparing the precursor pitch, had an optimal viscosity, and created a composition in which the aromatic planes were easily arranged in an orderly manner at the early stage of carbonization. We have discovered a raw material pitch that has excellent performance. In other words, the present invention maintains a relatively low softening point;
The present invention also provides a method for producing a raw material pitch that easily forms a mesophase. The present invention will be explained in detail below. In the present invention, a precursor pitch obtained by heating a raw material pitch is melt-spun, and then infusible and carbonized or graphitized to produce carbon fiber. 100 heavy oils with a boiling point of 200℃ or higher obtained through steam cracking
(2) A fraction with a boiling point within the range of 160 to 400°C generated when the raw material pitch is heat-treated is brought into contact with hydrogen in the presence of a hydrogenation catalyst, and the content is added to the fraction by volume. The aromatic nuclei of aromatic hydrocarbons that are
Add 10 to 200 parts by volume of hydrogenated oil obtained by 70% nuclear hydrogenation, and heat at a temperature of 370 to 480℃ and a pressure of 2 to 50 kg/
The present invention relates to a method for producing a raw material pitch for carbon fiber, characterized in that it is obtained by heat treatment at cm ² ·G. When the mesophase reaction is carried out using the raw material pitch obtained according to the present invention, not only the production of quinoline-insoluble components is suppressed, but also the pitch is modified,
It was completely unexpected that the final product, carbon fiber, could have a high modulus of elasticity and high strength. On the other hand, when coal tar pitch, commercially available petroleum pitch, or synthetic pitch was heat-treated to form a mesophase according to the method of JP-A-49-19127, the resulting pitch had a softening point of 340°C or higher. thing,
In many cases, melt spinning was practically impossible, such as in cases where solids were deposited, or even if solids were not deposited, the quinoline insoluble content reached 70% or more. Even if melt spinning is possible, the strength of the carbon fiber obtained by further infusibility, carbonization, and graphitization is 120 to 200 Kg/mm2, and the elastic modulus is 12 to 200 kg/ ^mm2.
It was ^around 20ton/mm2. Furthermore, when a material with a high softening point was spun, pores were present in the spun material due to the generation of thermal decomposition gas. Boiling point obtained when the petroleum used as component (1) of the raw material pitch in the present invention is subjected to steam decomposition
Heavy oil with a temperature of 200℃ or higher refers to oil with a boiling point range that is a by-product when producing olefins such as ethylene and propylene by steam cracking petroleum such as naphtha, kerosene, or light oil at 700 to 1200℃. Practically 200 ~
It is a heavy oil within the range of 450℃. The hydrogenated oil used as component (2) of the raw material pitch in the present invention refers to the hydrogenated oil that is produced when the raw material pitch is heat-treated and has a boiling point range of substantially 160 to 400°C, preferably 170 to 350°C. The fraction is brought into contact with hydrogen in the presence of a hydrogenation catalyst to partially hydrogenate the aromatic nuclei of aromatic hydrocarbons contained in the fraction. The hydrogenation catalyst used at this time may be a catalyst used in a normal hydrogenation reaction, for example, an inorganic solid such as bauxite, activated carbon, diatomaceous earth, zeolite, silica, titania, zirconia, alumina or silica gel is used as a carrier, copper etc. metals of group IB of the periodic table, metals of group B of the periodic table such as chromium, molybdenum, metals of group B of the periodic table such as cobalt, nickel, palladium or platinum in the form of metals or in the form of oxides or sulfides. Those supported on a carrier are used. Hydrogenation conditions vary depending on the type of catalyst used, but usually the temperature is 120 to 450°C, preferably 150 to 350°C, and the pressure is 20 to 100 Kg/cm ² G, preferably 30 to 70 Kg/cm. ²・G takes place. Further, when the hydrogenation treatment is carried out in a batch manner, the appropriate time for the hydrogenation treatment is 0.5 to 3 hours. When carried out in a continuous manner, a space velocity (LHSV) of 0.5 to 3.0 is selected. To give an example of hydrogenation conditions, 2wt% Raney
When the process is carried out batchwise using nickel as a catalyst, the pressure is preferably 40 to 50 kg/cm ² G, the temperature is 160 to 170°C, and the treatment time is 1 to 1.5 hours. When using the formula, the pressure is 30 to 50 kg/cm ² G, the temperature is about 330°C,
A space velocity (LHSV) of about 1.5 is preferably adopted. The aromatic nuclei of aromatic hydrocarbons contained in the fraction are partially hydrogenated by the hydrogenation reaction, but the nuclear hydrogen percentage at this time is 10 to 70%, preferably 15%.
~50%, most preferably 15-35%. Incidentally, the nuclear hydrogenation rate is defined by the following formula, and the number of aromatic ring carbon atoms in the following formula is as indicated by ASTM D-2140-66. Nuclear hydrogenation rate = (number of aromatic ring carbons before hydrogenation treatment) - (
Number of aromatic ring carbon atoms after hydrogenation treatment / number of aromatic ring carbon atoms before hydrogenation process The method for producing raw material pitch of the present invention specifies the heavy oil as component (1) and the hydrogenated oil as component (2). It can be obtained by mixing at a ratio of 1 and heating under specific conditions. The mixing ratio of component (1) heavy oil and component (2) hydrogenated oil is component (1):component (2) in a volume ratio of 1:0.1 to 2, preferably 1:0.2 to 1.5. It is necessary.
The heat treatment temperature is 370-480℃, preferably
Perform at a temperature within the range of 390-460°C. If the heat treatment temperature is lower than 370°C, the reaction progresses slowly and takes a long time, which is uneconomical. Further, heat treatment at a temperature higher than 480° C. causes problems such as caulking, which is not preferable. The heat treatment time is determined in consideration of the heat treatment temperature, and is performed for a long time when the temperature is low, and for a short time when the temperature is high. Generally, treatment times within the range of 15 minutes to 20 hours, preferably 30 minutes to 10 hours can be employed. Regarding the pressure, it can be carried out under any pressure, but it is preferably a pressure that does not substantially distill out the active ingredients in the raw materials unreacted to the outside of the system, specifically ² to 50 Kg/cm2.
G, preferably 5 to 30 kg/cm ² ·G. After the heat treatment, it is also preferable to remove light components by distillation or the like, if necessary. To explain the present invention with reference to FIG. 1, heavy oil, which is the component (1) of the raw material pitch of the present invention, is introduced from line 1, and hydrogenated oil, which is component (2), is introduced from line 3. After (1) and component (2) are mixed in a predetermined ratio, heat treatment is performed under predetermined conditions to prepare a raw material pitch. The prepared raw material pitch is then heat treated under specific conditions. The fraction produced at this time with a boiling point within the range of 160 to 400°C is extracted from line 2, subjected to partial nuclear hydrogenation treatment, and then returned through line 3 as a component of the raw material pitch. When carrying out the present invention, component (2) of the raw material pitch of the present invention is not present at the initial stage, but other oils may be substituted for component (2) of the present invention, or heat treatment may be performed without using component (2) of the present invention. At this time, the hydrogenated oil produced by partially hydrogenating the fraction with a boiling point range of substantially 160 to 400°C is substituted as component (2) of the raw material pitch of the present invention from the next step. The present invention can be achieved by following these steps. When other oils are substituted for component (2) of the present invention in the first step, the oils to be substituted include, for example:
The boiling point range obtained when petroleum is steam cracked is
Hydrogenated oil obtained by partial nuclear hydrogenation of a fraction within the range of 160 to 400℃, partial nuclear hydrogenation of a fraction with a boiling point range of 160 to 400℃ obtained when fluid catalytic cracking of petroleum is performed. Hydrogenated oil, component of the raw material pitch of the present invention (1)
Hydrogenated oil produced by partial nuclear hydrogenation of the fraction with a boiling point range of 160 to 400 degrees Celsius produced when heavy oil used as oil is heat-treated at 380 to 480 degrees Celsius, and when petroleum is subjected to fluid catalytic cracking. Naphthalene is a hydrogenated oil produced by partial nuclear hydrogenation of the fraction with a boiling point of 160 to 400 degrees Celsius that is produced when heavy oil with a boiling point of 200 degrees Celsius or higher is heat-treated at 380 degrees Celsius to 480 degrees Celsius. , indene, anthracene, phenanthrene, etc. 2- or 3-ring
Nuclear hydrides of cyclic aromatic hydrocarbons or oils similar to these can be exemplified as preferred oils. By using the raw material pitch of the present invention thus obtained, when heat-treated to form a mesophase, the production of high molecular weight components that are insoluble in quinoline is suppressed, and at the same time, the softening point of the pitch is prevented from increasing. Furthermore, it becomes a good precursor pitch having a composition in which the aromatic planes are easily arranged in an orderly manner. As a result, carbon fibers with extremely excellent elastic modulus and strength can be obtained. A known method can be used to produce carbon fiber using the raw material pitch obtained according to the present invention. That is, a raw material pitch is heat-treated to form a mesophase, the resulting precursor pitch is melt-spun, and then subjected to infusibility treatment and carbonization or further graphitization treatment to produce carbon fibers. The reaction at the stage of heat-treating the raw material pitch to convert it into a mesophase to obtain the precursor pitch is usually carried out at a temperature
It is carried out at 340 to 450°C, preferably 370 to 420°C, under normal pressure or reduced pressure and by bubbling inert gas such as nitrogen. The heat treatment time at this time can be arbitrarily determined depending on conditions such as temperature and amount of inert gas aeration, but it is usually carried out for 1 to 50 hours, preferably 3 to 20 hours. The amount of inert gas ventilation is
A pitch of 0.7 to 5.0 scfh/1b is preferred. As a method for melt-spinning the precursor pitch, known methods such as an extrusion method, a centrifugation method, and an atomization method can be used. The pitch fiber obtained by melt spinning is then subjected to an infusible treatment in an oxidizing gas atmosphere. As the oxidizing gas, one or more of oxidizing gases such as oxygen, ozone, air, nitrogen oxide, halogen, and sulfur dioxide gas are usually used. This infusibility treatment is carried out under temperature conditions that do not soften or deform the melt-spun pitch fibers to be treated. for example
Temperatures of 20-360°C, preferably 20-300°C are employed. Further, the treatment time is usually 5 minutes to 10 hours. The infusible pitch fibers are then carbonized or further graphitized in an inert gas atmosphere to obtain carbon fibers. Carbonization is usually carried out at a temperature of 800-2500°C. Generally, the processing time required for carbonization is 0.5 minutes ~
It is 10 hours. Further, when graphitizing is carried out, it is carried out at a temperature of 2500 to 3500°C, usually for 1 second to 1 hour. In addition, during infusibility, carbonization or graphitization treatment,
If necessary, a slight load or tension may be applied to the object to be processed in order to prevent shrinkage, deformation, etc. The present invention will be specifically explained below with reference to Examples, but the present invention is not limited thereto. Example 1 Heavy oil (A) with a boiling point of 200°C or higher, which was produced as a by-product when naphtha was steam cracked at 830°C, was collected. The properties of this heavy oil (A) are shown in Table 1. Next, the heavy oil (A) was heat treated at a pressure of 15 kg/cm ² ·G and a temperature of 400° C. for 3 hours. This heat-treated oil (B) was distilled at 250°C/1.0mmHg to remove light components to obtain pitch () with a softening point of 82°C. On the other hand, the heat-treated oil (B) was distilled at 250°C/1.0 mmHg to collect a fraction (C) with a boiling point of 160 to 400°C. Its properties are shown in Table 2. This fraction (C) was converted to a pressure of 35 kg using a nickel-molybdenum catalyst (NM-502).
Partial nuclear hydrogenation was carried out by contacting with hydrogen at cm ² ·G, temperature of 330°C, and space velocity (LHSV) of 1.5 to obtain hydrogenated oil (D). The nuclear hydrogenation rate was 31%. 50 parts by volume of the above-mentioned heavy oil (A) were mixed with 50 parts by volume of hydrogenated oil (D), and heat treated at a pressure of 20 kg/cm ² ·G and a temperature of 430° C. for 3 hours. This heat treated oil is heated to 250℃/1.0mm.
Distilled with Hg to remove light components, softening point 54℃,
Pitch () containing 0.9% by weight of benzene insoluble matter was prepared. Next, add nitrogen to 30g of this pitch ().
Stir with aeration at 550 ml/min, 10 min at 400°C.
Heat treatment was performed for a period of time, and a fraction (E) with a boiling point range of 160 to 400°C was collected during this heat treatment process. Its properties are shown in Table 3. 2wt% of Raney Nickel was suspended in this fraction (E) at a temperature of 166℃ and a hydrogen pressure of 40 to 50Kg/cm ² G.
Partial nuclear hydrogenation was performed for 1.5 hours to obtain hydrogenated oil (F). The nuclear hydrogenation rate at this time was 34%.

【table】

【table】

【table】

[Table] 80 parts by volume of heavy oil (A) and 20 parts by volume of hydrogenated oil (F) were mixed and heat treated at a pressure of 15 kg/cm ² ·G and a temperature of 430°C for 2 hours. This heat-treated oil was distilled under reduced pressure to remove light components, yielding raw material pitch with a softening point of 63°C. Next, for 30g of this raw material pitch, 550ml of nitrogen/
Stir with ventilation for 10 minutes and heat treat at 400℃ for 10 hours. Softening point: 289℃, quinoline insoluble content: 26.1
Pitch with a mesophase content of 59% by weight was obtained. This pitch was melt-spun at 345°C using a spinner with a nozzle diameter of 0.3 mmφ and L/D = 2 to produce pitch fibers of 10 to 18μ, and further infusible under the conditions shown below.
Carbonization and graphitization treatments were performed to obtain carbon fibers. The processing conditions for infusibility, carbonization and graphitization are as follows. Γ Infusibility conditions: Heat in an air atmosphere at a rate of 3°C/min up to 200°C, 1°C/min up to 300°C, and hold at 300°C for 10 minutes. Γ Carbonization conditions: Temperature raised at 10℃/min in nitrogen atmosphere.
Hold at 1000℃ for 30 minutes. Γ Graphitization conditions: Heat treatment up to 2500℃ at a heating rate of 50℃/min in an argon stream. The tensile strength of the obtained carbon fiber was 275Kg/mm ² and Young's modulus was 38Ton/mm ² . Comparative Example 1 Pitch () obtained in Example 1 was used as a raw material pitch and heat treated in the same manner as in Example 1, resulting in a softening point of 321°C, quinoline insoluble content of 57% by weight,
Pitch with a mesophase content of 98% was obtained. This pitch was melt-spun at 367°C using the spinning machine used in Example 1 to produce pitch fibers of 17 to 25μ, and treated with infusible, carbonized, and graphitized in the same manner as in Example 1 to produce carbon fibers. Obtained. The tensile strength of this carbon fiber is 120Kg/
mm ² , and the elastic modulus was 15Ton/mm ² .

[Brief explanation of drawings]

FIG. 1 is a process sheet showing the carbon fiber manufacturing process of the present invention.

Claims (1)

[Claims] 1 After melt-spinning a precursor pitch obtained by heating a raw material pitch, infusibility treatment and carbonization or further graphitization treatment is performed to produce carbon fiber. For 100 parts by volume of heavy oil with a boiling point of 200℃ or higher obtained when 10 to 200 parts by volume of hydrogenated oil obtained by hydrogenating 10 to 70% of the aromatic nuclei of aromatic hydrocarbons contained in the fraction by contacting with hydrogen in the presence of hydrogen, and at a temperature of 370 A method for producing a raw material pitch for carbon fiber, characterized in that it is obtained by heat treatment at ~480°C and a pressure of 2~50 kg/cm ² ·G.