CA2030150A1 - Process for making mesophase pitch - Google Patents
Process for making mesophase pitchInfo
- Publication number
- CA2030150A1 CA2030150A1 CA 2030150 CA2030150A CA2030150A1 CA 2030150 A1 CA2030150 A1 CA 2030150A1 CA 2030150 CA2030150 CA 2030150 CA 2030150 A CA2030150 A CA 2030150A CA 2030150 A1 CA2030150 A1 CA 2030150A1
- Authority
- CA
- Canada
- Prior art keywords
- mesophase
- gas
- sparging gas
- feedstock
- pitch
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 33
- 230000008569 process Effects 0.000 title claims abstract description 31
- 239000011302 mesophase pitch Substances 0.000 title claims abstract description 16
- 239000007789 gas Substances 0.000 claims abstract description 55
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000001301 oxygen Substances 0.000 claims abstract description 20
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 19
- 239000004917 carbon fiber Substances 0.000 claims abstract description 19
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 19
- 239000011261 inert gas Substances 0.000 claims abstract description 13
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000011337 anisotropic pitch Substances 0.000 claims abstract 5
- 239000011295 pitch Substances 0.000 claims description 43
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 15
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 238000010438 heat treatment Methods 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- -1 steam Substances 0.000 claims description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- 230000006872 improvement Effects 0.000 claims description 3
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 2
- 239000003546 flue gas Substances 0.000 claims description 2
- 235000019253 formic acid Nutrition 0.000 claims description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims description 2
- 229910052724 xenon Inorganic materials 0.000 claims description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001307 helium Substances 0.000 claims 1
- 229910052734 helium Inorganic materials 0.000 claims 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 abstract description 12
- 239000008246 gaseous mixture Substances 0.000 abstract 1
- 239000000306 component Substances 0.000 description 15
- 239000000047 product Substances 0.000 description 14
- 239000000835 fiber Substances 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 8
- 238000002791 soaking Methods 0.000 description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 239000000295 fuel oil Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011301 petroleum pitch Substances 0.000 description 3
- 239000010426 asphalt Substances 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000003763 carbonization Methods 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011269 tar Substances 0.000 description 2
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 description 1
- 206010001497 Agitation Diseases 0.000 description 1
- 239000001741 Ammonium adipate Substances 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 208000036366 Sensation of pressure Diseases 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000004523 catalytic cracking Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000007380 fibre production Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000004227 thermal cracking Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
Landscapes
- Inorganic Fibers (AREA)
- Working-Up Tar And Pitch (AREA)
Abstract
Case No. 7698 IMPROVED PROCESS FOR MAKING MESOPHASE PITCH
Abstract of the Disclosure An improved process for producing an anisotropic pitch product suitable for carbon fiber manufacture. A carbonaceous feedstock is heated at elevated temperature while passing a reac-tive sparging gas through the feedstock. The sparging gas is an oxidative gas such as a gaseous mixture containing a major proportion of inert gas and from about 0.1 to 2% by volume of oxygen. The process produces an anisotropic pitch having from 50 to 100% by volume mesophase which is suitable for producing good quality carbon fibers.
Abstract of the Disclosure An improved process for producing an anisotropic pitch product suitable for carbon fiber manufacture. A carbonaceous feedstock is heated at elevated temperature while passing a reac-tive sparging gas through the feedstock. The sparging gas is an oxidative gas such as a gaseous mixture containing a major proportion of inert gas and from about 0.1 to 2% by volume of oxygen. The process produces an anisotropic pitch having from 50 to 100% by volume mesophase which is suitable for producing good quality carbon fibers.
Description
~ ~ 3 ~
- 1 - Case No. 7698 IMPROVED PROCESS FOR MAKING MESOPHASE PITCH
Background oE the Invention 1. Field of the Invention The present invention pertains to an improved process for producing a carbonaceous pitch product having a mesophase content ranging from about 50 to 100%, which is suitable for carbon fiber manufacture. ~ore particularly, the invention relates to a process for making mesophase containing pitch capable of producing carbon fibers having enhanced properties, by use of an oxidatively reactive sparge gas during heat treatment of mesophase precursor.
- 1 - Case No. 7698 IMPROVED PROCESS FOR MAKING MESOPHASE PITCH
Background oE the Invention 1. Field of the Invention The present invention pertains to an improved process for producing a carbonaceous pitch product having a mesophase content ranging from about 50 to 100%, which is suitable for carbon fiber manufacture. ~ore particularly, the invention relates to a process for making mesophase containing pitch capable of producing carbon fibers having enhanced properties, by use of an oxidatively reactive sparge gas during heat treatment of mesophase precursor.
2. The Prior Art In recent years extensive patent literature has evolved concerning the conversion of carbonaceous pitch feed material into a mesophase-containing pitch which is suitable Eor the manu-facture of carbon fibers having desirable modulus of eLasci.city, tensile strength, and elongation characteristics.
U. S. Patent No. 4,209,500 which issued to Chwastialc on June 2~, 1980 is directed to the production of R high mesophase pitch that can be employed in the manufacture o~ carbon Eibers.
This patent is one of a series of patents pertaining to a process for producing mesophase pitches suitable for carbon fiber produc-: tion. Each of these patents broadly involves heat treating or heat soaking the carbonaceous feed while agitating and/or passing an inert gas therèthrough so as to produce a more suitable pitch product for the manufacture of carbon fibers.
As set forth in the Chwastiak patent, earlier U.S. patents 3,976,729 and 4,017,327 issued to Lewis et al involve agitating the carbonaceous starting material during the heat treatment.
The use of an inert sparge gas during heat treatment is found in U.S. Patents 3,974,264 and 4,026,788 issued to McHenry. Stirring or agitating the starting material while sparging with an inert gas is also disclosed in the McHenry patents.
The Chwastiak patent additionally discloses the prior state of the art, as well as the Lewis et al and McHenry patents discussed above, and these disclosures by Chwastiak in Column 1, 2~3~
line 13 to Column 2, line 50, are incorporated herein by reference.
Boeh the Lewis et al and McHenry proposals to promote mesophase formation had serious limitations, according to Chwastiak, in that their pitch products tended to segregate into two phase systems which hampered subsequent spinning operations.
Chwastiak proposed a mesophase-producing process wherein a single phase product resulted. The process requires both agita-tion and an inert gas sparge, the improvement resulting, according to Chwastiak, by passing the inert gas through the pitch at a rate of at least 4 standard cubic feet per hour (SCFH) per pound of pitch. In the illustration the heat treatment required 44 hours.
It would be advantageous therefore to provide a process which did not require such a high rate of inert gas flow and which also could be accomplished in less time without deleteriously affecting the pitch product.
In published German Patent ~pplication No, 3305-055-~
(Nippon Oil KK) there is disclosed a process wherein a pLtch feed is initially heat treated at 370 to 420C in a stream of inert gas for 5 to 20 hours under atmospheric or reduced pressure.
Subsequently, an oxidant gas such as air or oxygen is passed through the pitch at 200-350C., one atmosphere pressure, at a flow rate of 1.0 to 3.5 SCFH for 10 minutes to 2 hours. No increase in mesophase content was reported as a result of the separate treatment with the oxidant gas.
Koppers Co. Inc. has published DT 2221707-Q and ~T 2357477 patent applications, which disclose manufacture of isotropic carbon fibers wherein the starting material is first reacted with oxygen and then vacuum distilled, to remove non-oxidized lower-boiling components.
Summary of the Invention In accordance with the present invention, it has now been found that if a gas or gas mixture containing an effective, but not excessive, amount of an oxidatively reactive gas is sparged through a carbonaceous feedstock during heat soaking thereof, a pitch product containing 50 to 100% by volume mesophase, as determined by its optical anisotropy, results, and in a shorter -3- 2~3~J~
time than would be required without the reactive gas component~
This product, often substantially 100% mesophase, has a melting point suitable for fiber spinning and results in fibers having improved strength and elongation properties.
Thus, lt is essential in the invention to use an oxidative component in the sparging gas stream, and furthermore to control the reactivity oE the sparging gas such that iCs reactive component can promote the transformation to mesophase, without producLng an unacceptably high melting point pitch product. At the same time, the sparging gas removes from the feed material volatile components that are known to be undesirable in a mesophase pitch product used for the manufacture of carbon fibers. In addition the use of the sparging gas containing controlled amounts of an oxidative component further appears to affect the chemical and physical nature of the mesophase pitch product in such a manner that carbon Eibers spun thereErom are characterized by outstanding modulus of elasticity and high tensile strength as well as an improved elongation ratio.
Brief Description of the Drawing Figure 1 is a graph of heat soak time versus the amount of oxygen in the sparging as utilizing a fluid catalytic cracker (FCC) heavy oil feedstock under a fixed set of conditions.
Detailed Description of the Invention The term "pitch" as used herein means petroleum pitches, natural asphalt and heavy oil obtained as a by-product in the naphtha cracking industry, pitches of high carbon conteDt obtained from petroleum asphalt and other substances having properties of pitches produced as by-products in various industrial production processes.
The term "petroleum pitch" refers to the residuum carbona-ceous material obtained from the thermal and catalytic cracking of petroleum distillates.
Generally, pitches having a high degree of aromaticity are suitable for carrying out the present invention.
Carbonaceous pitches having an aromatic carbon content of from about 75% to about 90% as determined by nuclear magnetic ~3~
resonance spectroscopy are particularly useful in the process of this invention. So, too, are high boiling, highly aromatic streams containing such pitches or that are capable of being con-verted into such pitches.
On a weight basis, the useEul pitches will have from about 88% to about 93% carbon and from about 7/O to about 5% hydro-gen. I~hile elements other than carbon and hydrogen, such as sulfur and nitrogen, to mention a few, are normaLly present Ln such pitches, i~ is important that these other elements do not exceed about 4% by weight of the pitch. Also, these useful pitches typi-cally will have an average molecular weight of the order of about 200 to l,OOO.
Those petroleum pitches meeting the foregoing requirements are preferred starting materials for the practice of the present invention. Thus, it should be apparent that carbonaceous residues of petroleum origin, and particularly isotropic carbonaceous petro-leum pitches which are known to form mesophase in substantial amounts, for example in the order of about 90% by volume and higher, during heat treatment at elevated temperatures, for example in the range of 350C. to 450C., are especially preferred starting materials for the practice of the present invention.
In general, any petroleum or coal-derived heavy hydro-carbon fraction may be used as the carbonaceous feedstock in the process of this invention. Suitable feedstocks in addition to petroleum pitch include heavy aromatic petroleuM streams, ethylene cracker tars, coal derivatives, petroleum thermal tars, fluid catalytic cracker residues, and aromatic distillates having a boiling range of from 650-g50F. The use of petroleum pitch~type feed is preferred.
The preferred sparging gas comprises an inert component which is a gas or a mixture of gases which do not react with the feedstock at the heat soaking temperature and an oxidatively reac-tive gas or mixture of gases present in an amount effective to promote formation of mesophase but less than that amount which produces mesophase pitch having a melting point above about 400C, and preferably less than that amount which produces mesophase ~5~
pitch having a melting point above about 360C. Mesophase pitch having a melting point above about 360C is difficult to spin due to coke formation, and mesophase pitch melting above about 400C is virtually impossible to spin. An especially preferred sparging gas is nitrogen containing from 0.1 to 2.0 percent by volume oxygen.
Gases other than oxygen, such as ozone, hydrogen peroxide, nitrogen dioxide, formic acid vapor and hydrogen chloride vapor, may be used as the oxidative component. The amounts thereof would need to be selected to have an oxidative reactivity for the meso-phase forming feed equivalent to that provided by using from O.l to 2.0 percent by volume oxygen in inert gas.
The inert gaseous component of the sparging gas is a gas or mixture of gases which do not react with the feedstock at heat soaking conditions. Illustrative inert gases are nitrogen, argon, xenon, helLum, methane, hydrocarbon-based flue gas, steam, and mixtures thereof. In general, there can be employed any gas stream or a mixture of various gas streams with an appropriate oxidative component so that reaction with the feedstock or promotion oE the reaction between molecules in feedstock occurs. It is essential, however, that the reactive gas used for sparging reacts directly or indirectly, i.e. catalytically, with the feedstock to produce a mesophase pitch which has an increased mesophase content and which can be spun into high quality carbon fibers.
The sparging gas rate will be at least 0.1 SCFH per pound of feed, preferably from about 0.1 to 20 SCFH. Sparging is generally carried out at atmospheric or slightly elevated pres-sures, e.g. about 1 to 3 atmospheres. The sparging time period may vary widely depending on the feedstock, gas feed rates, and the like. For most purposes it will be carried out throughout the heat treatment or heat-soaking step, which often ranges from about 2 to 100 hours, but in some cases the oxidative component may be added for less than the full reaction period. As discussed above, the essential feature of the present invention is the use of a sparging gas containing a controlled amount of an oxidative component during the heat-soaking of the carbonaceous feedstock to form a pitch containing 50 to 100% by volume mesophase, as determined by its optical anisotropy. Thus, the sparge gas of the present invention promotes formation of mesophase from isotropic feedstock, i.e. ~he amount of mesophase increases to the desired range in a shorter period of time, while at the same time the sparging gas carries away volatile materials which are undesirable.
Further, the resulting mesophase is readily converted into carbon fibers with improved properties when compared with mesophase pro-duced at similar conditions but without use of an oxidatively reactive sparge gas component.
The mesophase pitch product of this invention may be spun into continuous anisotropic carbon fibers by conventional procedures such as melt spinning, followed by the separate steps of thermosetting and carbonization. As indicated, these are known techniques and consequently they do not constitute critical features of the present invention.
The present invention will be more fully understood by reference to the following illustrative embodiments.
A series of mesophase pitches was made from the heavy residual fraction (900F+ fraction) of a heavy oil from an FCC
unit by heat soaking at 385C and atmospheric pressure using a mixture of oxygen and nitrogen gas for sparging. Approximately 200 grams of the heavy residual oil was charged in a glass reactor with capacity around 340 ml for the heat soak step. Gas sparging through the reactor charge was controlled at 1.75 SCFH throughout the heat-soak step. The oxygen concentration in the sparging gas varied between 0.01 to 2.0 percent by volume. The melting ; 30 temperatures and the mesophase contents of the product pitches were determined by hot-stage microscopy. Table 1 shows the yields and properties of the mesophase pitches.
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~ U~ ~
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~ ~ o t~
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o ~ ~
~ ~E~
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~ r~ ) I
rd ~ I t~ tY
h ~rl P~ ~1 r I
~3~ O ~rl ~ 1~ l U) ~ ~ ~ O r~l a) ~, t)~ ` O O 5:~ ~t N
U~
~ O ~ ~
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H
Z ~
~~ `I ~ ~ ~ ~
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r~
. L~
0~ 00 00 CQ C~
cr-` 3 It is seen in Table 1 that the time required to produce 100% mesophase pitch is reduced and the product mesophase pitch yield is increased, as the amo~nt of oxygen in the sparging gas is increased. The mesophase pitches A, B, C, D and E were then spun into fiber filaments through a single hole spinneret. The as-spun fiber fLlaments were placed in an oven and heated in air from room temperature to 350C. at a rate of 4C/minute and then heated at 350C for 32 minutes, followed by carbonization in argon at a temperature of 1950C. The carbonized fibers were then tested as single filaments at a 2.54 cm gauge length and 10% elongation per minute. Table 2 shows the properties of the produced carbonized fibers.
Table 2 Properties of Produced Carbon Fibers Mesophase Tensile Pitch Stre~gth, Modu~us, Elongation x 10 psi x 10 psi Ratio, %
A 329 45 0.68 B 300 46 0.67 C 405 37 0.93 D 357 39 0.84 E 359 36 0.83 The results in Table 2 show that the fibers made from mesophase pitch prepared by adding a controlled amount of oxygen to the nitrogen sparging gas have higher elongation ratios than those made using high purity nitrogen ( < 0.01 Vol.% oxygen~ for sparging.
A series of mesophase pitches were made from heavy resi-dual fractions of heavy oils from an FCC unit. The reactor system and the operating conditions for heat soak are essentially the same as those described in the previous Example 1. In addition to the gas sparging through the reactor charge, a flow of high f~s~ ~J ~ . ~
purity nitrogen containing less than 0.001 Vol % oxygen was contin-uously purged through the open space underneath the reactor roof into the reactor overhead line at a rate of 1.75 SCFH. This purging step blanlceted the top portion o~ the reactor with inert gas.
The properties of the produced mesophase pitches are shown in Table 3.
2 ~
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~ a~
E~ u~
a) o c~ o O o~ o o o a~ ~ ~ ~
~C~
~ ~ U
O .,1 ~ C~
p:; ~ ~ ~1 ~ o a~
aJ a ~E~
t) ` ~ CO
~a ~1 ~ ~~O I I
o a~
. ~ ~ ~
t) ,l ~ o ~ ~0 c~
U~ o ~ O
æ o ~, O e o v o tv~ H O U~
t~7 Q
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.~ ~In u~ u~
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~ H ~ H ~I H ~C H
a) U rI U r-l U ~
a~ U-r1 U-~ U rl ~-rt S4 ~ O ¢1 0 ~1 0 ~4 0 The above produced mesophase pitches were then spun into fibers followed by stabilization in the same way as described in Example 1.
The fibers were then carbonized to 1800C. Table 4 shows the properties of the produced carbon fibers.
Table 4 Properties of Produced Carbon Fibers Mesophase Tensile Pitch Stre~gth, Modu6usElongation Sample x 10 psig x 10 ~ atio, /~
A' 316 34 0.92 B' 329 24 1.17 C' 401 50 0.73 D' 397 32 1.16 The results in Table 4 again demonstrate the enhancement of the elongation ratio of product fibers by adding a controlled amount of oxygen in the sparging gas.
Referring to Figure 1, the data show that when a sparge gas containing controlled amounts of oxygen as the oxidative compon-ent is employed, there is a significant reduction in the time necessary to convert the feedstock to a mesophase pitch suitable for carbon fiber production. Although the precise reason for this is not known for certain, it is believed that the reactive } or oxidative component in the sparging gas reacts witb aromatic molecules in the feed to form some type of free radicals which then lead to a higher degree of polymerization via free radical chain reaction.
Various changes and modifications can be made in the process of this invention without departing from the spirit and scope thereof. The various embodiments which have been described herein are for the purpose of illustrating the invention, and are not intended to limit it.
U. S. Patent No. 4,209,500 which issued to Chwastialc on June 2~, 1980 is directed to the production of R high mesophase pitch that can be employed in the manufacture o~ carbon Eibers.
This patent is one of a series of patents pertaining to a process for producing mesophase pitches suitable for carbon fiber produc-: tion. Each of these patents broadly involves heat treating or heat soaking the carbonaceous feed while agitating and/or passing an inert gas therèthrough so as to produce a more suitable pitch product for the manufacture of carbon fibers.
As set forth in the Chwastiak patent, earlier U.S. patents 3,976,729 and 4,017,327 issued to Lewis et al involve agitating the carbonaceous starting material during the heat treatment.
The use of an inert sparge gas during heat treatment is found in U.S. Patents 3,974,264 and 4,026,788 issued to McHenry. Stirring or agitating the starting material while sparging with an inert gas is also disclosed in the McHenry patents.
The Chwastiak patent additionally discloses the prior state of the art, as well as the Lewis et al and McHenry patents discussed above, and these disclosures by Chwastiak in Column 1, 2~3~
line 13 to Column 2, line 50, are incorporated herein by reference.
Boeh the Lewis et al and McHenry proposals to promote mesophase formation had serious limitations, according to Chwastiak, in that their pitch products tended to segregate into two phase systems which hampered subsequent spinning operations.
Chwastiak proposed a mesophase-producing process wherein a single phase product resulted. The process requires both agita-tion and an inert gas sparge, the improvement resulting, according to Chwastiak, by passing the inert gas through the pitch at a rate of at least 4 standard cubic feet per hour (SCFH) per pound of pitch. In the illustration the heat treatment required 44 hours.
It would be advantageous therefore to provide a process which did not require such a high rate of inert gas flow and which also could be accomplished in less time without deleteriously affecting the pitch product.
In published German Patent ~pplication No, 3305-055-~
(Nippon Oil KK) there is disclosed a process wherein a pLtch feed is initially heat treated at 370 to 420C in a stream of inert gas for 5 to 20 hours under atmospheric or reduced pressure.
Subsequently, an oxidant gas such as air or oxygen is passed through the pitch at 200-350C., one atmosphere pressure, at a flow rate of 1.0 to 3.5 SCFH for 10 minutes to 2 hours. No increase in mesophase content was reported as a result of the separate treatment with the oxidant gas.
Koppers Co. Inc. has published DT 2221707-Q and ~T 2357477 patent applications, which disclose manufacture of isotropic carbon fibers wherein the starting material is first reacted with oxygen and then vacuum distilled, to remove non-oxidized lower-boiling components.
Summary of the Invention In accordance with the present invention, it has now been found that if a gas or gas mixture containing an effective, but not excessive, amount of an oxidatively reactive gas is sparged through a carbonaceous feedstock during heat soaking thereof, a pitch product containing 50 to 100% by volume mesophase, as determined by its optical anisotropy, results, and in a shorter -3- 2~3~J~
time than would be required without the reactive gas component~
This product, often substantially 100% mesophase, has a melting point suitable for fiber spinning and results in fibers having improved strength and elongation properties.
Thus, lt is essential in the invention to use an oxidative component in the sparging gas stream, and furthermore to control the reactivity oE the sparging gas such that iCs reactive component can promote the transformation to mesophase, without producLng an unacceptably high melting point pitch product. At the same time, the sparging gas removes from the feed material volatile components that are known to be undesirable in a mesophase pitch product used for the manufacture of carbon fibers. In addition the use of the sparging gas containing controlled amounts of an oxidative component further appears to affect the chemical and physical nature of the mesophase pitch product in such a manner that carbon Eibers spun thereErom are characterized by outstanding modulus of elasticity and high tensile strength as well as an improved elongation ratio.
Brief Description of the Drawing Figure 1 is a graph of heat soak time versus the amount of oxygen in the sparging as utilizing a fluid catalytic cracker (FCC) heavy oil feedstock under a fixed set of conditions.
Detailed Description of the Invention The term "pitch" as used herein means petroleum pitches, natural asphalt and heavy oil obtained as a by-product in the naphtha cracking industry, pitches of high carbon conteDt obtained from petroleum asphalt and other substances having properties of pitches produced as by-products in various industrial production processes.
The term "petroleum pitch" refers to the residuum carbona-ceous material obtained from the thermal and catalytic cracking of petroleum distillates.
Generally, pitches having a high degree of aromaticity are suitable for carrying out the present invention.
Carbonaceous pitches having an aromatic carbon content of from about 75% to about 90% as determined by nuclear magnetic ~3~
resonance spectroscopy are particularly useful in the process of this invention. So, too, are high boiling, highly aromatic streams containing such pitches or that are capable of being con-verted into such pitches.
On a weight basis, the useEul pitches will have from about 88% to about 93% carbon and from about 7/O to about 5% hydro-gen. I~hile elements other than carbon and hydrogen, such as sulfur and nitrogen, to mention a few, are normaLly present Ln such pitches, i~ is important that these other elements do not exceed about 4% by weight of the pitch. Also, these useful pitches typi-cally will have an average molecular weight of the order of about 200 to l,OOO.
Those petroleum pitches meeting the foregoing requirements are preferred starting materials for the practice of the present invention. Thus, it should be apparent that carbonaceous residues of petroleum origin, and particularly isotropic carbonaceous petro-leum pitches which are known to form mesophase in substantial amounts, for example in the order of about 90% by volume and higher, during heat treatment at elevated temperatures, for example in the range of 350C. to 450C., are especially preferred starting materials for the practice of the present invention.
In general, any petroleum or coal-derived heavy hydro-carbon fraction may be used as the carbonaceous feedstock in the process of this invention. Suitable feedstocks in addition to petroleum pitch include heavy aromatic petroleuM streams, ethylene cracker tars, coal derivatives, petroleum thermal tars, fluid catalytic cracker residues, and aromatic distillates having a boiling range of from 650-g50F. The use of petroleum pitch~type feed is preferred.
The preferred sparging gas comprises an inert component which is a gas or a mixture of gases which do not react with the feedstock at the heat soaking temperature and an oxidatively reac-tive gas or mixture of gases present in an amount effective to promote formation of mesophase but less than that amount which produces mesophase pitch having a melting point above about 400C, and preferably less than that amount which produces mesophase ~5~
pitch having a melting point above about 360C. Mesophase pitch having a melting point above about 360C is difficult to spin due to coke formation, and mesophase pitch melting above about 400C is virtually impossible to spin. An especially preferred sparging gas is nitrogen containing from 0.1 to 2.0 percent by volume oxygen.
Gases other than oxygen, such as ozone, hydrogen peroxide, nitrogen dioxide, formic acid vapor and hydrogen chloride vapor, may be used as the oxidative component. The amounts thereof would need to be selected to have an oxidative reactivity for the meso-phase forming feed equivalent to that provided by using from O.l to 2.0 percent by volume oxygen in inert gas.
The inert gaseous component of the sparging gas is a gas or mixture of gases which do not react with the feedstock at heat soaking conditions. Illustrative inert gases are nitrogen, argon, xenon, helLum, methane, hydrocarbon-based flue gas, steam, and mixtures thereof. In general, there can be employed any gas stream or a mixture of various gas streams with an appropriate oxidative component so that reaction with the feedstock or promotion oE the reaction between molecules in feedstock occurs. It is essential, however, that the reactive gas used for sparging reacts directly or indirectly, i.e. catalytically, with the feedstock to produce a mesophase pitch which has an increased mesophase content and which can be spun into high quality carbon fibers.
The sparging gas rate will be at least 0.1 SCFH per pound of feed, preferably from about 0.1 to 20 SCFH. Sparging is generally carried out at atmospheric or slightly elevated pres-sures, e.g. about 1 to 3 atmospheres. The sparging time period may vary widely depending on the feedstock, gas feed rates, and the like. For most purposes it will be carried out throughout the heat treatment or heat-soaking step, which often ranges from about 2 to 100 hours, but in some cases the oxidative component may be added for less than the full reaction period. As discussed above, the essential feature of the present invention is the use of a sparging gas containing a controlled amount of an oxidative component during the heat-soaking of the carbonaceous feedstock to form a pitch containing 50 to 100% by volume mesophase, as determined by its optical anisotropy. Thus, the sparge gas of the present invention promotes formation of mesophase from isotropic feedstock, i.e. ~he amount of mesophase increases to the desired range in a shorter period of time, while at the same time the sparging gas carries away volatile materials which are undesirable.
Further, the resulting mesophase is readily converted into carbon fibers with improved properties when compared with mesophase pro-duced at similar conditions but without use of an oxidatively reactive sparge gas component.
The mesophase pitch product of this invention may be spun into continuous anisotropic carbon fibers by conventional procedures such as melt spinning, followed by the separate steps of thermosetting and carbonization. As indicated, these are known techniques and consequently they do not constitute critical features of the present invention.
The present invention will be more fully understood by reference to the following illustrative embodiments.
A series of mesophase pitches was made from the heavy residual fraction (900F+ fraction) of a heavy oil from an FCC
unit by heat soaking at 385C and atmospheric pressure using a mixture of oxygen and nitrogen gas for sparging. Approximately 200 grams of the heavy residual oil was charged in a glass reactor with capacity around 340 ml for the heat soak step. Gas sparging through the reactor charge was controlled at 1.75 SCFH throughout the heat-soak step. The oxygen concentration in the sparging gas varied between 0.01 to 2.0 percent by volume. The melting ; 30 temperatures and the mesophase contents of the product pitches were determined by hot-stage microscopy. Table 1 shows the yields and properties of the mesophase pitches.
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cr-` 3 It is seen in Table 1 that the time required to produce 100% mesophase pitch is reduced and the product mesophase pitch yield is increased, as the amo~nt of oxygen in the sparging gas is increased. The mesophase pitches A, B, C, D and E were then spun into fiber filaments through a single hole spinneret. The as-spun fiber fLlaments were placed in an oven and heated in air from room temperature to 350C. at a rate of 4C/minute and then heated at 350C for 32 minutes, followed by carbonization in argon at a temperature of 1950C. The carbonized fibers were then tested as single filaments at a 2.54 cm gauge length and 10% elongation per minute. Table 2 shows the properties of the produced carbonized fibers.
Table 2 Properties of Produced Carbon Fibers Mesophase Tensile Pitch Stre~gth, Modu~us, Elongation x 10 psi x 10 psi Ratio, %
A 329 45 0.68 B 300 46 0.67 C 405 37 0.93 D 357 39 0.84 E 359 36 0.83 The results in Table 2 show that the fibers made from mesophase pitch prepared by adding a controlled amount of oxygen to the nitrogen sparging gas have higher elongation ratios than those made using high purity nitrogen ( < 0.01 Vol.% oxygen~ for sparging.
A series of mesophase pitches were made from heavy resi-dual fractions of heavy oils from an FCC unit. The reactor system and the operating conditions for heat soak are essentially the same as those described in the previous Example 1. In addition to the gas sparging through the reactor charge, a flow of high f~s~ ~J ~ . ~
purity nitrogen containing less than 0.001 Vol % oxygen was contin-uously purged through the open space underneath the reactor roof into the reactor overhead line at a rate of 1.75 SCFH. This purging step blanlceted the top portion o~ the reactor with inert gas.
The properties of the produced mesophase pitches are shown in Table 3.
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a~ U-r1 U-~ U rl ~-rt S4 ~ O ¢1 0 ~1 0 ~4 0 The above produced mesophase pitches were then spun into fibers followed by stabilization in the same way as described in Example 1.
The fibers were then carbonized to 1800C. Table 4 shows the properties of the produced carbon fibers.
Table 4 Properties of Produced Carbon Fibers Mesophase Tensile Pitch Stre~gth, Modu6usElongation Sample x 10 psig x 10 ~ atio, /~
A' 316 34 0.92 B' 329 24 1.17 C' 401 50 0.73 D' 397 32 1.16 The results in Table 4 again demonstrate the enhancement of the elongation ratio of product fibers by adding a controlled amount of oxygen in the sparging gas.
Referring to Figure 1, the data show that when a sparge gas containing controlled amounts of oxygen as the oxidative compon-ent is employed, there is a significant reduction in the time necessary to convert the feedstock to a mesophase pitch suitable for carbon fiber production. Although the precise reason for this is not known for certain, it is believed that the reactive } or oxidative component in the sparging gas reacts witb aromatic molecules in the feed to form some type of free radicals which then lead to a higher degree of polymerization via free radical chain reaction.
Various changes and modifications can be made in the process of this invention without departing from the spirit and scope thereof. The various embodiments which have been described herein are for the purpose of illustrating the invention, and are not intended to limit it.
Claims (15)
1. In a process for producing a pitch product having a mesophase content of from 50 to 100% by volume and suitable for carbon fiber manufacture, which process comprises heating a carbonaceous feedstock at mesophase-forming temperature while passing a sparging gas therethrough for a time sufficient to produce said pitch product having said mesophase content, the improvement wherein said sparging gas includes an oxidatively reactive gaseous component in an amount (a) sufficient to produce said amount of mesophase content in a shorter time than would be required without said oxidatively reactive gaseous component, and (b) less than that amount which produces a pitch product having a melting point above 400°C.
2. The process of Claim 1 wherein said oxidatively reactive gaseous component is selected from the group consisting of oxygen, ozone, hydrogen peroxide, formic acid vapor, hydrogen chloride vapor, and mixtures thereof.
3. The process of Claim 1 wherein said sparging gas consists essentially of from 0.1 to 2.0 volume percent oxygen and the balance inert gas.
4. The process of Claim 1 wherein said pitch product is substantially 100 percent mesophase with a melting point not greater than 360°C.
5. The process of Claim 1 wherein said feedstock is heated at a temperature ranging from about 350°C to 450°C for a time of from 2 to 100 hours and said sparging gas consists essentially of from 0.1 to 2.0 volume percent oxygen with the balance being inert, said sparging gas being introduced at a rate of from 0.1 to 20 SCFH per pound of feedstock.
6. A process for producing an anisotropic pitch having a mesophase content of from 50 to 100% and suitable for carbon fiber manufacture, which process comprises heating a carbonaceous feedstock at a temperature ranging from about 350° to 450°C to produce mesophase while passing a sparging gas through said feed-stock at a rate of at least 0.1 SCFH per pound of feedstock, said sparging gas comprising an oxidatively reactive gaseous component in an amount effective to promote formation of said mesophase.
7. The process of Claim 6 wherein said feedstock is a pitch.
8. The process of Claim 6 wherein said anisotropic pitch product contains from about 90 to 100% mesophase.
9. The process of Claim 6 wherein said sparging gas contains oxygen in an amount of from 0.1 to 2.0 percent by volume.
10. The process of Claim 6 wherein said sparging gas consists essentially of said reactive gaseous component and an inert gas selected from the group consisting of nitrogen, argon, xenon, helium, methane, hydrocarbon-based flue gas, steam, and mixtures thereof.
11. The process of Claim 10 wherein said inert gas is nitrogen.
12. The process of Claim 10 wherein the sparging gas rate ranges from about 0.1 to 20 SCFH per pound of feedstock.
13. In a process for preparing a mesophase pitch product comprising passing a sparging gas through a carbonaceous feedstock that is being heated at elevated temperatures to produce mesophase, the improvement which comprises utilizing a sparging gas comprising an oxidatively reactive component in an amount effective to produce an anisotropic pitch product having from 50 to 100% mesophase and suitable for the manufacture of carbon fibers of improved properties.
14. The process of Claim 13 wherein said oxidatively reactive component is oxygen.
15. The process of Claim 14 wherein the remainder of said sparging gas is nitrogen.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA 2030150 CA2030150A1 (en) | 1990-11-16 | 1990-11-16 | Process for making mesophase pitch |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CA 2030150 CA2030150A1 (en) | 1990-11-16 | 1990-11-16 | Process for making mesophase pitch |
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CA2030150A1 true CA2030150A1 (en) | 1992-05-17 |
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CA 2030150 Abandoned CA2030150A1 (en) | 1990-11-16 | 1990-11-16 | Process for making mesophase pitch |
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CA (1) | CA2030150A1 (en) |
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1990
- 1990-11-16 CA CA 2030150 patent/CA2030150A1/en not_active Abandoned
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