WO1998050168A1 - Corrosion resistant composites useful in chemical reactors - Google Patents
Corrosion resistant composites useful in chemical reactors Download PDFInfo
- Publication number
- WO1998050168A1 WO1998050168A1 PCT/US1998/008620 US9808620W WO9850168A1 WO 1998050168 A1 WO1998050168 A1 WO 1998050168A1 US 9808620 W US9808620 W US 9808620W WO 9850168 A1 WO9850168 A1 WO 9850168A1
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- carbon
- component
- high purity
- chemical
- composite
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/71—Ceramic products containing macroscopic reinforcing agents
- C04B35/78—Ceramic products containing macroscopic reinforcing agents containing non-metallic materials
- C04B35/80—Fibres, filaments, whiskers, platelets, or the like
- C04B35/83—Carbon fibres in a carbon matrix
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- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
- C30B15/10—Crucibles or containers for supporting the melt
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B15/00—Single-crystal growth by pulling from a melt, e.g. Czochralski method
- C30B15/14—Heating of the melt or the crystallised materials
-
- C—CHEMISTRY; METALLURGY
- C30—CRYSTAL GROWTH
- C30B—SINGLE-CRYSTAL GROWTH; UNIDIRECTIONAL SOLIDIFICATION OF EUTECTIC MATERIAL OR UNIDIRECTIONAL DEMIXING OF EUTECTOID MATERIAL; REFINING BY ZONE-MELTING OF MATERIAL; PRODUCTION OF A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; SINGLE CRYSTALS OR HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; AFTER-TREATMENT OF SINGLE CRYSTALS OR A HOMOGENEOUS POLYCRYSTALLINE MATERIAL WITH DEFINED STRUCTURE; APPARATUS THEREFOR
- C30B35/00—Apparatus not otherwise provided for, specially adapted for the growth, production or after-treatment of single crystals or of a homogeneous polycrystalline material with defined structure
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- 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
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/10—Chemical after-treatment of artificial filaments or the like during manufacture of carbon
- D01F11/12—Chemical after-treatment of artificial filaments or the like during manufacture of carbon with inorganic substances ; Intercalation
- D01F11/125—Carbon
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E20/00—Combustion technologies with mitigation potential
- Y02E20/16—Combined cycle power plant [CCPP], or combined cycle gas turbine [CCGT]
- Y02E20/18—Integrated gasification combined cycle [IGCC], e.g. combined with carbon capture and storage [CCS]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/30—Self-sustaining carbon mass or layer with impregnant or other layer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2926—Coated or impregnated inorganic fiber fabric
- Y10T442/2984—Coated or impregnated carbon or carbonaceous fiber fabric
Definitions
- the present invention is directed to high purity composites of carbon fiber within a carbon matrix and their preparation. More particularly, the present invention is directed to high purity composites useful as corrosion resistant components for use in, or as part of, chemical process reactors.
- the precious metal group includes silver, gold and platinum. These metals are used in a variety of high performance applications where their outstanding corrosion resistance and catalytic behavior prove useful Despite the history of the use of aqua regia and the effort expended in reclaiming the precious metals, severe problems are still encountered due to the difficulty in manipulating and containing this highly corrosive acid, which comprises a 3: 1 or 4: 1 mixture of hydrochloric and nitric acids, and which will dissolve most metals rapidly. Conventional equipment capable of handling this acid is usually made from ceramics or glass. Problems associated with poor durability and poor shock resistance frequently occur, posing severe safety hazards, and in some cases leading to significant financial losses.
- Chemical reactors usually contain various plates, baffles, stirrers, trays, tubes and the like, which are usually made from steel or other metals. In certain chemical reactions, these parts have to be replaced on a frequent basis due to the high level of corrosion that takes place. Replacement of these parts means lengthy reactor downtime with serious economic consequences.
- High temperature composite materials in which a ceramic or carbon matrix is reinforced with a continuous fiber, find use in a variety of applications.
- One common application for composite materials is in aircraft brakes.
- the friction, or braking, material is made from a carbon matrix reinforced with carbon fibers (carbon carbon or C/C).
- Such materials have high mechanical strength and are capable of operating at extreme temperatures, up to 3000 °C (in a non-oxidizing atmosphere).
- Composites in which both the reinforcing fiber and the matrix are ceramic find use in specialty applications such as aircraft engine parts where both strength at high temperature and low weight are needed.
- Carbon/carbon based composites offer outstanding chemical resistance. This coupled with their lightweight and structural performance makes them ideal candidates for chemical processing equipment. An added advantage is that, according to the present invention, such materials can be produced at extremely high levels of purity, thus minimizing the risks of product contamination.
- the present invention provides a corrosion resistant, high purity carbon/carbon composite structural material consisting of carbon fiber reinforcements within a carbon matrix. This material has outstanding thermal properties, especially in non-oxidizing atmospheres.
- use of carbon/carbon composite materials in the chemical process industry was not known. This was due to the inability to produce materials that not only exhibit good structural and mechanical properties, but that are extremely pure and will not contaminate sensitive chemical species such as food additives, catalysts, pharmaceutical compounds and the like.
- the present invention therefore, provides a corrosion resistant, high purity composite comprising a continuous carbon fiber reinforced carbon matrix, having a total level of metal impurity below about 10 ppm, preferably below about 5 ppm, having an ultimate tensile strength of greater than about 25 ksi and a fracture toughness as measured by Izod impact of about 5 ft-lb/in.
- the present invention further provides chemical processing components comprising the above corrosion resistant, high purity carbon/carbon composite, the composite including a continuous carbon fiber reinforced carbon matrix having a total level of metal impurity below about 10 ppm, preferably below about 5 ppm, having an ultimate tensile strength of greater than about 25 ksi and a fracture toughness as measured by Izod impact of about 5 ft-lb/in.
- Such components can be used in processes for catalyst production of fine chemicals such as catalysts, food additives, pharmaceuticals, and the like, as well as industrial chemicals.
- the present invention provides a chemical process reactor floor or tray comprising the corrosion resistant, high purity carbon/carbon composite material.
- the present invention provides a reactor baffle comprising the corrosion resistant, high purity carbon/carbon material.
- the present invention provides a tray of the type widely used in distillation columns, comprising the corrosion resistant, high purity carbon/carbon material.
- the present invention also provides a chemical process apparatus comprising at least one corrosion resistant, high purity, carbon/carbon composite component, said high purity composite including a continuous carbon fiber reinforced carbon matrix having a total level of metal impurity below about 10 ppm, preferably below about 5 ppm, and most preferably the metal impurity being below the detection limit of inductively coupled plasma spectroscopy for the metals Ag, Al, Ba, Be, Ca, Cd, Co, Cr, Cu, K, Mg, Mn, Mo, Na, Ni, P, Pb, Sr and Zn.
- the chemical process reactor vessel comprises the corrosion resistant, high purity carbon/carbon composite.
- the present invention also provides a process for the production of a corrosion resistant, high purity, carbon/carbon composite comprising: heating a carbon fiber reinforcement to at least about 2400° C, impregnating the carbon fiber with a matrix precursor of high purity carbon having less than about 10 ppm metals, carbonizing the impregnated fabric to form a carbonized part, densifying the carbonized part with high purity carbon having less than about 10 ppm metals to form a component, and heating the component at a temperature of at least about 2400 °C to form the high purity composite.
- densifying the carbonized part includes purging a chemical vapor deposition (CVD) processing furnace with an inert gas at a temperature of at least about 2400°C, and densifying the carbonized part with chemically vapor deposited carbon in the purged CVD furnace to form the component.
- CVD chemical vapor deposition
- the present invention therefore includes a process utilizing at least one chemical processing component, wherein said component is in contact with at least one of i) a high purity material, such as for processing, and ii) a corrosive process media, wherein said component comprises a component according to the present invention, as described herein.
- the present invention therefore includes a process for treating precious metals including treating a material comprising at least one precious metal, wherein the at least one component of the present invention described herein is in contact with a process media comprising aqua regia.
- Carbon fiber reinforced carbon matrix materials, or carbon/carbon composites have thermal stability, high resistance to thermal shock due to high thermal conductivity and low thermal expansion behavior (that is, thermal expansion coefficient or TEC), chemical resistance, and have high toughness, strength and stiffness in high-temperature applications.
- thermal expansion coefficient or TEC thermal expansion coefficient
- Carbon/carbon composites comprise carbon reinforcements mixed or contacted with matrix precursors to form a "green” composite, which is then carbonized to form the carbon/carbon composite. They may also comprise carbon or graphite reinforcements in which the matrix is introduced fully or in part by chemical vapor infiltration (CVI).
- CVI chemical vapor infiltration
- the carbon reinforcements are commercially available from Amoco,
- DuPont, Hercules, and others can take the form of continuous fiber, cloth or fabric, yarn, and tape (unidirectional arrays of fibers).
- Yarns may be woven into desired shapes by braiding, knitting, or by multidirectional weaving.
- the yarn, cloth and/or tape may be wrapped or wound around a mandrel to form a variety of shapes and reinforcement orientations.
- the fibers may be wrapped in the dry state or they may be impregnated with the desired matrix precursor prior to wrapping, winding, or stacking.
- Such prepreg and woven structures reinforcements are commercially available from various sources, including Fiberite, Hexcel and Cytek.
- the reinforcements are prepared from precursors such as polyacrylonitrile (PAN), rayon or pitch. According to the preferred embodiment of the present invention, the reinforcement is in the form of continuous fibers, more preferably in the form of a woven cloth.
- Matrix precursors which may be used to form carbon/carbon composites according to the present invention include liquid sources of carbon, such as phenolic resins and pitch, and gaseous sources, including hydrocarbons such as methane, ethane, propane and the like.
- Representative phenolics include, but are not limited to, phenolics sold under the trade designations USP 39 and 91LD, such as supplied by Ashland Chemical, and SC1008 such as supplied by Borden Chemical.
- the carbon/carbon composites useful in the present invention may be fabricated by a variety of techniques.
- resin impregnated carbon fibers are autoclave- or press-molded into the desired shape on a tool or in a die.
- lay-ups of two dimensional (2D) continuous fiber or woven fabrics may be formed on a lay-up tool in the desired shape.
- the molded parts are heat-treated in an inert environment to temperatures from about 700 °C to about 2900°C in order to convert the organic phases to carbon.
- the carbonized parts are then densified by carbon chemical vapor infiltration (CVI) or by multiple cycle reimpregnations and carbonizations with the resins described above.
- CVI carbon chemical vapor infiltration
- the piece can be readily machined to precise tolerances, on the order of about 0.1 mm or less. Further, because of the strength and machinability of carbon carbon composites, in addition to the shaping possible in the initial fabrication process, carbon/carbon composites can be formed into shapes for components that are not possible with graphite, for example.
- the high purity carbon/carbon composite according to the present invention has the physical properties of conventionally produced carbon/carbon composites, yet has improved corrosion resistance and purity resulting from the process for the production of the corrosion resistant, high purity carbon/carbon composite of the present invention.
- the component After the component has been formed by the densification of the carbonized part, the component is further heat treated at 2400 °C to about 3000°C in a non-oxidizing or inert atmosphere to ensure graphitization of the structure and to remove any impurities that may have been introduced.
- the period of time for this procedure is calculated based upon graphitization time/temperature kinetics, taking into account furnace thermal load and mass.
- the component may be machined, if desired, to precise specifications and tolerances, as discussed above.
- Component purity is established by the use of high purity matrix precursors and carbon black fillers.
- the phenolic resins used should contain less than 50 ppm metals, should utilize non-metallic accelerators for cure, and preferably should be made in a stainless steel reactor. Processing conditions in the manufacture of the carbonized parts are maintained at high standards so as not to introduce any extraneous impurities.
- corrosion resistance means that the material experiences negligible attack, or exhibits negligible weight loss in commonly used chemical reaction media.
- strong oxidizing agents such as nitric acid
- mild oxidizing agents and all reducing agents have no effect on the material.
- High purity carbon/carbon composites prepared according to the present invention were analyzed by inductively coupled plasma spectroscopy (ICP) in comparison with conventional graphite components, also analyzed by atomic absorption spectroscopy (AAS), and with conventional carbon/carbon composites, analyzed by high temperature halonization.
- ICP inductively coupled plasma spectroscopy
- AS atomic absorption spectroscopy
- Table II Table 2 - Purity Levels in Graphite, Conventional C/C and C/C of the Present Invention
- the high purity carbon/carbon composites of the present invention are below the detection limit for inductively coupled plasma spectroscopy analysis for the metals Al, Ca, Cr, Cu, K, Mg, Mn, Mo, Na, Ni, and P, while these metal impurities are shown to be present in graphite, and in conventional carbon carbon composite materials (except in the latter, for nickel and potassium). Values reported herein that are lower than the ICP detection limit were obtained by glow discharge mass spectrometry. Carbon/carbon composites produced according to the invention were ashed and the diluted residue further analyzed by inductively coupled plasma spectroscopy for metals content in addition to those metals tested above. As demonstrated in Table 3 below, the concentration of these metals, Ag, Ba, Be, Cd, Co, Pb, Sr, and Zn, was also below the detection limit for the analytical technique.
- Carbon/carbon composites can be used in chemical processing apparatus without first coating the component, although it is preferable to precoat the carbon/carbon composite prior to use, in order to lock down any particles which may have formed as a result of the composite fabrication or machining process.
- Carbon/carbon composites can readily be coated with a protective coating, such as refractory carbides, refractory nitrides, and refractory borides.
- Preferred refractory coatings are silicon carbide, silicon nitride, boron carbide, boron nitride, pyrolytic boron nitride and silicon boride.
- Graded or layered coatings of the carbides, nitrides and borides may also be used.
- Other protective coatings which can be used to seal the carbon/carbon composite material, such as to avoid particulation, include glasses, vitreous or glassy carbon, and pyrolitic carbon.
- polymers such as fluorocarbon polymers, which are resistant to the reaction medium employed in the apparatus may also be used to coat the carbon/carbon composite components of the present invention, to prevent particulation.
- fluorocarbon polymers which are resistant to the reaction medium employed in the apparatus may also be used to coat the carbon/carbon composite components of the present invention, to prevent particulation. Examples include but are not limited to polytetrafluoroethylene, polyvinylidene fluoride, polymers of fluorinated ethylene-propylene, chlorotrifluoroethylene, hexafluoropropylene, and the like.
- the high purity, corrosion resistant carbon/carbon composites of the present invention can be produced to exhibit a density of about 1.6 to about 2 g/cc, and a porosity of about 2 to about 25% .
- These high purity composites generally range in tensile strength from about 25 to about 100 ksi, in tensile modulus up to about 30 msi, in flexural strength up to about 60 ksi, in compressive strength up to about 50 ksi, and in fractural toughness, as measured by Izod impact, from about 5 to about 25 ft- lb/in.
- Such inventive high purity composites exhibit a thermal conductivity of about 20 to about 500 W/mK in plane and about 5 to about 200 W/mK cross-ply, thermal expansion coefficients of zero to about 2 xlO "6 in in/°C in plane and about 6 xlO "6 in/in/°C to about 10 xlO "6 in/in/°F cross ply.
- Thermal emissivity of the high purity composites is about 0.4 to about 0.8.
- the electrical resistivity of the high purity composites is about 1 xlO "4 to about 1 x 10 "2 ohm-cm.
- the high purity, corrosion resistant carbon/carbon composites are formed into components for use in chemical process reactors, such as containers, plates, baffles, spargers, stirrers, screens, trays, tubes, pipes, lines, beds, tanks, liners, shields, diffuser plates, reactor floors, and the like, as well as the reactor vessel itself.
- a chemical processing "component” includes parts of a chemical processing apparatus, furniture or parts used within a chemical processing apparatus or its associated apparatus such as transport lines, distillation columns, valves, heaters, pump components, and the like, as well as all, or portions of the reactor vessel itself.
- chemical process reactor components such as diffuser plates have been fabricated, comprising a high purity, corrosion resistant composite including a carbon fiber reinforced carbon matrix having a level of total metal impurity below about 10 ppm.
- These diffuser plates act as supports for reactant particles within the reactor, and contain holes through which the reaction medium passes to contact the reactant particles.
- These and other components are preferably fabricated from composites having a total metal impurity level below about 5ppm, and most preferably below the detection limit of inductively coupled spectroscopy for the metals Ag, Al, Ba, Be, Ca, Cd, Co, Cr, Cu, K, Mg, Mn, Mo, Na, Ni, P, Pb, Sr and Zn.
- a high purity carbon fiber fabric is partly densified with high purity CVD carbon in order to rigidize the fabric and to give it structural integrity, having a fabric tensile strength on the order of about 90 to about
- the partly densified component is utilized as a mesh or screen to support catalyst particles in the reaction medium.
- Precious metal catalysts such as those disclosed in US Patent 4,600,571 are usually prepared by the deposition of a precious metal halide, e.g. ruthenium, onto a suitable substrate, e.g. carbon particles, followed by reduction of the metal halide to the metal.
- a precious metal halide e.g. ruthenium
- Such catalysts may be used in the production of ammonia.
- Such processes used to manufacture such catalysts may include depositing the metal halide onto the catalyst substrate from a solution of the halide in hydrochloric acid. Such reaction usually occurs between 100 and 200°C.
- Stainless steel components in the catalyst reactor are known to have a limited lifetime due to severe corrosion of the steel by the metal halide/hydrochloric acid medium. Such parts have to be replaced on a regular basis, which results in undesirable reactor downtime.
- the use of the carbon/carbon parts according to the present invention not only provides reduced reactor downtime but installation of large parts, e.g. reactor floors, is simplified due to the much reduced weight of the component made with the inventive composite as compared to that of stainless steel.
- the high level of purity of the inventive carbon/carbon parts reduces the chances of contamination of the catalyst.
- Acetic acid or acetic anhydride, for example, is used as the starting point for many industrial chemicals.
- Other acids such as adipic acid, is used in the manufacture of man-made plastics such as nylon.
- coal gasification turns high sulfur coal into low sulfur coal gas, which is subsequently burned.
- coal is turned into electricity.
- a gasifier produces fuel gases which are cleaned, and then burned in a gas turbine to produce electricity.
- the fuel gas produced is extremely corrosive and comprises ammonia, carbon monoxide, hydrochloric acid and other corrosive substances, present in the process at temperatures up to 900° C. This fuel gas attacks most known metals, making the handling of the fuel gas and subsequent burning extremely difficult.
- the following advantages have been realized using the high purity, corrosion resistant composite components of the present invention in chemical processing apparatus.
- the improved corrosion resistance as compared to metals, as well as the durability of the high purity carbon/carbon composite components results in a reduction in reactor downtime and in some instances, reactor rebuild.
- the durability of the high purity carbon carbon composite components is due to their superior thermal and mechanical properties.
- the high purity composites are also resistant to thermal shock and heat/cool cycles, offering an improvement over conventional graphite components. Other advantageous thermal characteristics are listed in Table 4, above.
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- Organic Chemistry (AREA)
- Materials Engineering (AREA)
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- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
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Abstract
Description
Claims
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA 2287892 CA2287892A1 (en) | 1997-05-02 | 1998-04-29 | Corrosion resistant composites useful in chemical reactors |
| EP98918848A EP0977637A4 (en) | 1997-05-02 | 1998-04-29 | Corrosion resistant composites useful in chemical reactors |
| JP54818898A JP2000516904A (en) | 1997-05-02 | 1998-04-29 | Corrosion resistant composites useful in chemical reactors |
| AU71693/98A AU7169398A (en) | 1997-05-02 | 1998-04-29 | Corrosion resistant composites useful in chemical reactors |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/850,205 US6068925A (en) | 1995-02-27 | 1997-05-02 | Corrosion resistant composites useful in chemical reactors |
| US08/879,982 US5989504A (en) | 1995-02-27 | 1997-06-20 | Chemical process employing corrosion resistant composites |
| US08/850,205 | 1997-06-20 | ||
| US08/879,982 | 1997-06-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1998050168A1 true WO1998050168A1 (en) | 1998-11-12 |
Family
ID=27126912
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/US1998/008620 Ceased WO1998050168A1 (en) | 1997-05-02 | 1998-04-29 | Corrosion resistant composites useful in chemical reactors |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5989504A (en) |
| EP (1) | EP0977637A4 (en) |
| JP (1) | JP2000516904A (en) |
| AU (1) | AU7169398A (en) |
| CA (1) | CA2287892A1 (en) |
| TW (1) | TW565585B (en) |
| WO (1) | WO1998050168A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2550375A1 (en) * | 2014-05-05 | 2015-11-06 | Mespack, Sl | Portapinzas cart for horizontal machine automatic forming and filler of flexible packaging (Machine-translation by Google Translate, not legally binding) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6699427B2 (en) | 2002-07-26 | 2004-03-02 | Ucar Carbon Company Inc. | Manufacture of carbon/carbon composites by hot pressing |
| US20040155382A1 (en) * | 2002-12-03 | 2004-08-12 | Dai Huang | Manufacture of carbon/carbon composites by hot pressing |
| US7207424B2 (en) * | 2002-12-03 | 2007-04-24 | Ucar Carbon Company Inc. | Manufacture of carbon/carbon composites by hot pressing |
| US6878331B2 (en) * | 2002-12-03 | 2005-04-12 | Ucar Carbon Company Inc. | Manufacture of carbon composites by hot pressing |
| JP4387159B2 (en) * | 2003-10-28 | 2009-12-16 | 東洋炭素株式会社 | Graphite material, carbon fiber reinforced carbon composite material, and expanded graphite sheet |
| FR2864465B1 (en) * | 2003-12-31 | 2007-10-19 | Arkema | REINFORCED FLUORINATED POLYMER PLATES, PROCESSES OF MAKING, REACTORS CONTAINING THESE CORROSION-RESISTANT PLATES, METHODS OF MAKING THE SAME, AND FLUORINATION METHODS THEREOF IN THESE REACTORS |
| JP4342466B2 (en) * | 2005-03-31 | 2009-10-14 | 株式会社東芝 | Quantitative analysis of trace metal elements |
| FR2925531B1 (en) * | 2007-12-20 | 2010-01-15 | Snecma Propulsion Solide | SUPPORT DEVICE FOR ELECTRODES IN AN ELECTROLYSIS INSTALLATION |
| US10899671B2 (en) * | 2016-08-24 | 2021-01-26 | Westinghouse Electric Company Llc | Process for manufacturing SiC composite ceramics |
| US20200062654A1 (en) * | 2018-08-13 | 2020-02-27 | Skc Solmics Co., Ltd. | Boron carbide sintered body and etcher including the same |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4894286A (en) * | 1988-11-07 | 1990-01-16 | Rohr Industries, Inc. | Oxidation resistant refractory coated carbon-carbon composites |
| US5132145A (en) * | 1987-04-27 | 1992-07-21 | Societe Anonyme | Method of making composite material crucible for use in a device for making single crystals |
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| Publication number | Priority date | Publication date | Assignee | Title |
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1997
- 1997-06-20 US US08/879,982 patent/US5989504A/en not_active Expired - Fee Related
-
1998
- 1998-04-29 WO PCT/US1998/008620 patent/WO1998050168A1/en not_active Ceased
- 1998-04-29 EP EP98918848A patent/EP0977637A4/en not_active Withdrawn
- 1998-04-29 JP JP54818898A patent/JP2000516904A/en active Pending
- 1998-04-29 AU AU71693/98A patent/AU7169398A/en not_active Abandoned
- 1998-04-29 CA CA 2287892 patent/CA2287892A1/en not_active Abandoned
- 1998-05-11 TW TW87107226A patent/TW565585B/en not_active IP Right Cessation
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| US5132145A (en) * | 1987-04-27 | 1992-07-21 | Societe Anonyme | Method of making composite material crucible for use in a device for making single crystals |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2550375A1 (en) * | 2014-05-05 | 2015-11-06 | Mespack, Sl | Portapinzas cart for horizontal machine automatic forming and filler of flexible packaging (Machine-translation by Google Translate, not legally binding) |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2287892A1 (en) | 1998-11-12 |
| EP0977637A1 (en) | 2000-02-09 |
| AU7169398A (en) | 1998-11-27 |
| JP2000516904A (en) | 2000-12-19 |
| US5989504A (en) | 1999-11-23 |
| TW565585B (en) | 2003-12-11 |
| EP0977637A4 (en) | 2001-02-21 |
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