Classifications

• • C—CHEMISTRY; METALLURGY
  • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
  • C10C—WORKING-UP PITCH, ASPHALT, BITUMEN, TAR; PYROLIGNEOUS ACID
  • C10C3/00—Working-up pitch, asphalt, bitumen
• • D—TEXTILES; PAPER
  • D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
  • D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
  • D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
  • D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
  • D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
  • D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
  • D01F9/145—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from pitch or distillation residues

Definitions

• the invention relates to a mesophase pitch and particularly relates to a mesophase pitch containing at least about 70% by weight mesophase and a process for producing the mesophase pitch and carbon fibers from the mesophase pitch.
• Mesophase pitch has been known to be suitable for producing carbon fibers having excellent properties suitable for commercial exploitation. It is known that mrso- phase derived carbon fibers are lightweight, strong, stiff, electrically conductive and both chemically and thermally inert. The mesophase derived carbon fibers perform well ss reinforcements in composites and have found use in aerospace applications and quality sporting equipment.
• carbon fibers have been primarily made from three types of precursor materials: rayon, polyacrylonitrile (PAN), and pitch.
• PAN polyacrylonitrile
• pitch The use of pitch as a precursor is attractive economically.
• carbon fibers produced from mesophase pitch exhibit high preferred molecular orientation and relatively excellent mechanical properties.
• pitch is to be understood as used in the instant art and generally refers to a carbonaceous residue consisting of a complex mixture of primarily aromatic organic compounds which are solid at room temperature and exhibit a relatively broad melting or softening temperature range. When cooled from the melt, the pitches behave as glasses.
• mesophase is to be understood as used in the instant art and generally is synonymous with liquid crystal. That is, a state of matter which is intermediate between crystalline solid and a normal liquid. Ordinarily, a material in the mesophase state exhibits both anisotropic and liquid properties.
• mesophase-containing pitch is a pitch containing less than about 40% by weight mesophase and the non-mesophase portion or isotropic phase is the.continuous phase.
• mesophase pitch is a pitch containing more than about 40% by weight mesophase and is capable of forming a continuous anisotropic phase when dispersed by agitation or the like in accordance with the prior art.
• the conventional method for preparing mesophase pitch from a precursor pitch includes heat treating at a temperature greater than 350°C.to effect thermal polymerization. This process produces large molecular weight molecules capable of forming mesophase.
• a typical conventional method is carried out using reactors maintained at about 400°C for about 20 hours.
• the properties of the final material can be controlled by the reaction temperature, heat- treatment time, and volatilization rate.
• the presence of the high molecular weight fraction results in a melting point of the mesophase pitch of at least 330 . C.
• An even higher temperature is needed to transform the mesophase pitch into fibers. This is termed "spinning" in the art.
• the amount of mesophase in pitch can be evaluated by known methods using polarized light microscopy.
• the presence of homogeneous bulk mesophase regions can be visually observed by polarized light microscopy and quantitatively determined by the method disclosed in the aforementioned Chwastiak patent.
• the criteria of insolubility in certain organic solvents such as quinoline and pyridine was used to estimate mesophase content.
• certain non-mesophase insolubles could, however, be present in the precursor pitch certain non-mesophase insolubles and it is a common practice to remove these insolubles before treating the precursor pitch.
• % Q. I.” refers to quinoline insolubles of a pitch quinoline extracted at 75°C.
• % P. I.” refers to pyridine insolubles of a pitch by Soxhlet extraction in boiling pyridine at about 115°C.
• Softening point or softening temperature of a pitch is related to its molecular weight constitution, the presence of a large amount of high molecular weight components generally tends to raise the softening temperature. It is a common practice in the art to characterize in part a precursor pitch by its softening point. For mesophase pitches, the softening point is used to determine, suitable spinning temperature. Generally, the spinning temperature is about 40°C or more higher than the softening temperature.
• Mettler softening point procedure is widely accepted as the standard for evaluating precursor pitches. This procedure can be adapted for use on mesophase pitches.
• the softening temperature of a-mesophase pitch can also be determined by hot stage microscopy.
• the mesophase pitch is heated on a microscope hot stage in an inert atmosphere under polarized light.
• the temperature of the mesophase pitch is raised under a controlled rate and the temperature at which the mesophase pitch commences to deform is noted as the softening temperature.
• softening point or softening temperature will refer to the temperature determined by the Mettler procedure for both precursor and mesophase pitches.
• a mesophase pitch containing at least about 70% by weight mesophase produced from physical operations without chemical operations on a carbonaceous precursor pitch so that the mesophase pitch possesses a molecular weight distribution wherein at least about 75% of the molecules have a molecular weight in the range of from about 600 to about 1300, less than about 10% of the molecules have a molecular weight less than about 600; and less than about 15% of the molecules have a molecular weight more than about 1300.
• the mesophase pitch of the invention possesses x-ray properites of interlayer spacing Co/2 of less than about 3.60 Angstroms and an apparent stack height Lc of greater than about 20 Angstroms.
• the mesophase.pitch of the invention contains at least about 90% by weight mesophase and more preferably about 100% by weight mesophase.
• the physical operations which can be used on the carbonaceous precursor pitch include devolatilizing, solvent extraction, a sequence of solvent extraction; chromatographic separation such as gel permeation chromatography, vacuum sublimation, blending of different pitches any one of which might have been subjected to the same operation, and combinations of the foregoing.
• a pitch fiber formed from the mesophase pitch may be formed without any chemical operations e.g. by spinning.
• the spinning is at a temperature less than about 370°C.
• Conventional spinning does not subject the pitch to a chemical change for a temperature below about 370°C. for the period of time the mesophase pitch is at that elevated temperature.
• the instant invention allows the formation of a pitch fiber from a carbonaceous pitch without any chemical operations.
• the solvents suitable for treating the carbonaceous pitch include toluene, benzene, N, N-dimethyl formamide, a mixture of toluene and petroleum ether, and carbon disulfide, of course, numerous other solvents are suitable, particulary among conventional pitch solvents.
• the suitability of a solvent can be determined easily in accordance with the instant disclosure.
• Some solvents which were found unacceptable for obtaining at least about 70% by weight mesophase for certain pitches include nitromethane, acetonitrile, ethylacetate, and methyl ethyl ketone. It appears that the solubility parameter of the solvents is not indicative of the suitability of the solvent.
• the carbonaceous precursor pitch is heated to effect polymerization.
• the resultant mesophase pitch is characterized by a molecular weight distribution which contains two major peaks.
• the low molecular weight peak corresponds to components of the precursor pitch and the high molecular weight peak corresponds to the molecules produced by the thermal polymerization.
• the instant mesophase pitch possesses. a molecular weight distribution having a single major peak generally positioned between the two peaks which would have arisen if the thermal polymerization had been carried out.
• the carbonaceous precursor pitch suitable for carrying out the invention should be a precursor pitch capable of forming a large-domained mesophase pitch by conventional thermal porcesses as set forth in the aforementioned Singer patent no. 4,005,183.
• the suitability of any carbonaceous pitch can be determined in a straight forward manner in accordance with the teachings herein.
• a commercially available petroleum pitch was used in a solvent extraction operation.
• the petroleum pitch had a softening temperature of about 130°C and had 0% P.I. and contained no mesophase.
• Example 1 was repeated except that boiling toluene was used.
• the yield was 6% by weight and the mesophase content was about 100% by weight.
• a commercially available petroleum pitch different from the Example 1 was selected.
• the petroleum pitch had a softening temperature of about 123°C and had about 0% P.I. and contained no mesophase.
• Example 1 The operations of the:Example 1 were repeated except that the solvent was a 1:2 mixture of petroleum ether and toluene. About 14% by weight yield was obtained and the yield had a.softening temperature of about 239°C and had about 3% P.I. and contained about 100% by weight mesophase.
• Example 3 was repeated.except that the solvent was a 1:1 mixture of petroleum ether and toluene. The yield was about 32% and contained about' 50% by weight mesophase.
• the mesophase pitch of the.Example 3 was spun into fibers on a monofilament spinning machine at about 290°C.
• the fibers had a diameter of about 20 microns and were thermoset by heating them in air at 2°C per minute to about 375°C.
• the thermoset fibers were examined by polarized light microscopy and were determined to contain about 100% anisotropic state.
• the thermoset fibers were carbonized to 1700°C in an inert atmosphere in accordance with conventional methods and tests on the carbonized fibers exhibited a modulus of about 25 x 10 6 psi (172 GPa) and 250,000 psi (1.72 GPa) tensile strength.
• a third type of commercially available petroleum pitch was selected.
• the petroleum pitch had a softening temperature of about 130°C.
• the pitch. was first distilled and the new softening temperature was about 201°C with about 3% P.I. and 3% by weight mesophase.
• the pitch was solvent extracted as in the Example 1 to give a yield of about 36% by weight, 41% P.I., and about 90% by weight mesophase.
• the softening temperature of the mesophase pitch was about 343°C.
• Example 6 was repeated except that the solvent extraction was carried out with boiling toluene. About 30% by weight yield was obtained with a softening temperature of about 360°C. The yield had about 69% P.I. and contained about 100% by weight mesophase.
• Example 7 was repeated except that the solvent extraction was carried out with benzene at a temperature of about 80°C.
• the yield was about 30% by weight and had about 35% P.I. and contained about 100% by weight mesophase.
• the softening temperature was about 360°C.
• the petroleum pitch of the Example 6 was heated at a temperature of about 390°C under an inert gas purge for about one hour to remove the lowest molecular weight components. About 21% by weight was distilled off and the remaining pitch had a softening temperature of about 162°C, exhibited 0% P.I., and contained no mesophase.
• Solvent extraction was carried out at room temperature by stirring 2400 ml of toluene with 120 grams of . ground up pitch. After filtering through a sintered glass filter using vacuum suction, the yield was about 19% by weight. The yield had a softening temperature of about 320°C, exhibited about 39% P.I., and contained about 80% by weight mesophase.
• Example 10 was repeated except that the solvent extraction was carried out at about 110°C.
• the yield was about 7% by weight.
• the yield had a softening temperature of about 370°C, exhibited about 64% P.I., and contained about 100% by weight mesophase.
• the distilled pitch of the Example 6 was solvent extracted with boiling benzene by refluxing 50 grams of the powdered pitch with 1000 ml for about two hours.
• the hot solution was filtered on a sintered glass funnel and the yield was about 30% by weight.
• the yield had a softening temperature of about 360°C, exhibited about 55% P.I., and contained about 100% by weight mesophase.
• Example 6 was repeated except that there was no prior distillation. No insolubles were obtained.
• the petroleum pitch of the Example 3 was solvent extracted with petroleum ether.
• the yield was about 77% by weight and contained no mesophase.
• Further solvent extraction with toluene in accordance with the Example 3 produced about 1% by weight yield which contained about 100% by weight mesophase.
• Solvent extraction was carried out on a coal tar pitch having a softening temperature of about 125°C, and about 0% mesophase. At room temperature, 60 grams of pitch was stirred with 1200 ml of toluene for about two hours. The yield was about 47% by weight. The yield had a softening temperature of about 318°C, exhibited about 53% P.I., and contained about 60% by weight mesophase.
• the coal tar pitch of the Example 15 was solvent extracted by refluxing 29.5:grams of the pitch with 500 ml of toluene at a temperature of about 110°C for about two hours.
• a 40% by weight yield contained about 85% by weight mesophase.
• Tests were carried out to determine mesophase content as a function of blending soluble and insoluble portions of the solvent extracted pitch.
• Tests were carried out on the various yields from the examples to determine the characteristics of both the molecular weight distributions and x-ray diffraction.
• Table 1 shows the results of these tests for - mesophase pitches of various examples.
• the molecular weight distribution data was obtained in accordance with the aforementioned Lewis et al. patent no. 3,976,729 and Chwastiak British patent 2,005,293.
• the solvent employed in the gel permeation chromatographic procedure was quinoline.
• Table 2 shows mesophase pitches produced by conventional thermal processes for pitches used in various examples.
• Table 3 shows x-ray data for precursor pitches prior to any operations.
• the mesophase pitch of the Example 3 was melted at a temperature of about 300°C and stirred for about 30 minutes in an inert atmosphere in order to remove the solvent.
• the product was spun-into monofilaments at a temperature of about 300°C.
• the as-spun fibers had a diameter of 15 microns and 25 microns.
• the 25 micron fibers were crushed to a powder and examined by x-ray.
• the Co/2 was measured as 3.54 Angstrom and Lc was measured as 34 Angstrom.
• the preferred orientation of the as-spun fibers was measured as being about 30.
• the as-spun fibers made by conventional processes as disclosed in the aforementioned Singer patent no. 4,032,430 had a Co/2 of from 3.45 to 3.55 Angstroms, Lc of from 30 to 50 Angstroms, and a preferred orientation of from 25° to 30°.
• the 15 micron fibers were thermoset by heating in air at 2° per minute to about 375°C.
• the thermoset fibers were examined and contained about 100% anisotropic state.
• the thermoset fibers were carbonized to 1700°C in an inert atmosphere in accordance with conventional methods and the carbonized fibers exhibited a modulus of about 28 x 10 6 psi (193 GPa) and a tensile strength of 273,000 psi (1.88 GPa).

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• Chemical Kinetics & Catalysis (AREA)
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• Textile Engineering (AREA)
• Civil Engineering (AREA)
• Structural Engineering (AREA)
• Materials Engineering (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Organic Chemistry (AREA)
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• Inorganic Fibers (AREA)

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• 1980
  • 1980-09-25 JP JP13363480A patent/JPS5657881A/ja active Granted
  • 1980-09-26 DE DE8080303384T patent/DE3070671D1/de not_active Expired
  • 1980-09-26 EP EP19800303384 patent/EP0026647B1/fr not_active Expired

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