carbon fiber
| Dictionary: carbon fiber |
n.
An extremely strong thin fiber made by pyrolyzing synthetic fibers, such as rayon, until charred. It is used to make high-strength composites.
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carbon fiber |
Chemistry Dictionary:
carbon fibres |
Fibres of carbon in which the carbon has an oriented crystal structure. Carbon fibres are made by heating textile fibres and are used in strong composite materials for use at high temperatures.
How Products are Made:
How is a carbon fiber made? |
Background
A carbon fiber is a long, thin strand of material about 0.0002-0.0004 in (0.005-0.010 mm) in diameter and composed mostly of carbon atoms. The carbon atoms are bonded together in microscopic crystals that are more or less aligned parallel to the long axis of the fiber. The crystal alignment makes the fiber incredibly strong for its size. Several thousand carbon fibers are twisted together to form a yarn, which may be used by itself or woven into a fabric. The yarn or fabric is combined with epoxy and wound or molded into shape to form various composite materials. Carbon fiber-reinforced composite materials are used to make aircraft and spacecraft parts, racing car bodies, golf club shafts, bicycle frames, fishing rods, automobile springs, sailboat masts, and many other components where light weight and high strength are needed.
Carbon fibers were developed in the 1950s as a reinforcement for high-temperature molded plastic components on missiles. The first fibers were manufactured by heating strands of rayon until they carbonized. This process proved to be inefficient, as the resulting fibers contained only about 20% carbon and had low strength and stiffness properties. In the early 1960s, a process was developed using polyacrylonitrile as a raw material. This produced a carbon fiber that contained about 55% carbon and had much better properties. The polyacrylonitrile conversion process quickly became the primary method for producing carbon fibers.
During the 1970s, experimental work to find alternative raw materials led to the introduction of carbon fibers made from a petroleum pitch derived from oil processing. These fibers contained about 85% carbon and had excellent flexural strength. Unfortunately, they had only limited compression strength and were not widely accepted.
Today, carbon fibers are an important part of many products, and new applications are being developed every year. The United States, Japan, and Western Europe are the leading producers of carbon fibers.
Classification of Carbon Fibers
Carbon fibers are classified by the tensile modulus of the fiber. Tensile modulus is a measure of how much pulling force a certain diameter fiber can exert without breaking. The English unit of measurement is pounds of force per square inch of cross-sectional area, or psi. Carbon fibers classified as "low modulus" have a tensile modulus below 34.8 million psi (240 million kPa). Other classifications, in ascending order of tensile modulus, include "standard modulus," "intermediate modulus," "high modulus," and "ultrahigh modulus." Ultrahigh modulus carbon fibers have a tensile modulus of 72.5-145.0 million psi (500 million-1.0 billion kPa). As a comparison, steel has a tensile modulus of about 29 million psi (200 million kPa). Thus, the strongest carbon fiber is about five times stronger than steel.
The term graphite fiber refers to certain ultrahigh modulus fibers made from petroleum pitch. These fibers have an internal structure that closely approximates the three-dimensional crystal alignment that is characteristic of a pure form of carbon known as graphite.
Raw Materials
The raw material used to make carbon fiber is called the precursor. About 90% of the carbon fibers produced are made from polyacrylonitrile. The remaining 10% are made from rayon or petroleum pitch. All of these materials are organic polymers, characterized by long strings of molecules bound together by carbon atoms. The exact composition of each precursor varies from one company to another and is generally considered a trade secret.
During the manufacturing process, a variety of gases and liquids are used. Some of these materials are designed to react with the fiber to achieve a specific effect. Other materials are designed not to react or to prevent certain reactions with the fiber. As with the precursors, the exact compositions of many of these process materials are considered trade secrets.
The Manufacturing
Process
The process for making carbon fibers is part chemical and part mechanical. The precursor is drawn into long strands or fibers and then heated to a very high temperature with-out allowing it to come in contact with oxygen. Without oxygen, the fiber cannot burn. Instead, the high temperature causes the atoms in the fiber to vibrate violently until most of the non-carbon atoms are expelled. This process is called carbonization and leaves a fiber composed of long, tightly inter-locked chains of carbon atoms with only a few non-carbon atoms remaining.
Here is a typical sequence of operations used to form carbon fibers from polyacrylonitrile.
Spinning
- Acrylonitrile plastic powder is mixed with another plastic, like methyl acrylate or methyl methacrylate, and is reacted with a catalyst in a conventional suspension or solution polymerization process to form a polyacrylonitrile plastic.
- The plastic is then spun into fibers using one of several different methods. In some methods, the plastic is mixed with certain chemicals and pumped through tiny jets into a chemical bath or quench chamber where the plastic coagulates and solidifies into fibers. This is similar to the process used to form polyacrylic textile fibers. In other methods, the plastic mixture is heated and pumped through tiny jets into a chamber where the solvents evaporate, leaving a solid fiber. The spinning step is important because the internal atomic structure of the fiber is formed during this process.
- The fibers are then washed and stretched to the desired fiber diameter. The stretching helps align the molecules within the fiber and provides the basis for the formation of the tightly bonded carbon crystals after carbonization.
Stabilizing
- Before the fibers are carbonized, they need to be chemically altered to convert their linear atomic bonding to a more thermally stable ladder bonding. This is accomplished by heating the fibers in air to about 390-590° F (200-300° C) for 30-120 minutes. This causes the fibers to pick up oxygen molecules from the air and rearrange their atomic bonding pattern. The stabilizing chemical reactions are complex and involve several steps, some of which occur simultaneously. They also generate their own heat, which must be controlled to avoid overheating the fibers. Commercially, the stabilization process uses a variety of equipment and techniques. In some processes, the fibers are drawn through a series of heated chambers. In others, the fibers pass over hot rollers and through beds of loose materials held in suspension by a flow of hot air. Some processes use heated air mixed with certain gases that chemically accelerate the stabilization.
Carbonizing
- Once the fibers are stabilized, they are heated to a temperature of about 1,830-5,500° F (1,000-3,000° C) for several minutes in a furnace filled with a gas mixture that does not contain oxygen. The lack of oxygen prevents the fibers from burning in the very high temperatures. The gas pressure inside the furnace is kept higher than the outside air pressure and the points where the fibers enter and exit the furnace are sealed to keep oxygen from entering. As the fibers are heated, they begin to lose their non-carbon atoms, plus a few carbon atoms, in the form of various gases including water vapor, ammonia, carbon monoxide, carbon dioxide, hydrogen, nitrogen, and others. As the non-carbon atoms are expelled, the remaining carbon atoms form tightly bonded carbon crystals that are aligned more or less parallel to the long axis of the fiber. In some processes, two furnaces operating at two different temperatures are used to better control the rate de heating during carbonization.
Treating the surface
- After carbonizing, the fibers have a surface that does not bond well with the epoxies and other materials used in composite materials. To give the fibers better bonding properties, their surface is slightly oxidized. The addition of oxygen atoms to the surface provides better chemical bonding properties and also etches and roughens the surface for better mechanical bonding properties. Oxidation can be achieved by immersing the fibers in various gases such as air, carbon dioxide, or ozone; or in various liquids such as sodium hypochlorite or nitric acid. The fibers can also be coated electrolytically by making the fibers the positive terminal in a bath filled with various electrically conductive materials. The surface treatment process must be carefully controlled to avoid forming tiny surface defects, such as pits, which could cause fiber failure.
Sizing
- After the surface treatment, the fibers are coated to protect them from damage during winding or weaving. This process is called sizing. Coating materials are chosen to be compatible with the adhesive used to form composite materials. Typical coating materials include epoxy, polyester, nylon, urethane, and others.
- The coated fibers are wound onto cylinders called bobbins. The bobbins are loaded into a spinning machine and the fibers are twisted into yarns of various sizes.
Quality Control
The very small size of carbon fibers does not allow visual inspection as a quality control method. Instead, producing consistent precursor fibers and closely controlling the manufacturing process used to turn them into carbon fibers controls the quality. Process variables such as time, temperature, gas flow, and chemical composition are closely monitored during each stage of the production.
The carbon fibers, as well as the finished composite materials, are also subject to rigorous testing. Common fiber tests include density, strength, amount of sizing, and others. In 1990, the Suppliers of Advanced Composite Materials Association established standards for carbon fiber testing methods, which are now used throughout the industry.
Health and Safety Concerns
There are three areas of concern in the production and handling of carbon fibers: dust inhalation, skin irritation, and the effect of fibers on electrical equipment.
During processing, pieces of carbon fibers can break off and circulate in the air in the form of a fine dust. Industrial health studies have shown that, unlike some asbestos fibers, carbon fibers are too large to be a health hazard when inhaled. They can be an irritant, however, and people working in the area should wear protective masks.
The carbon fibers can also cause skin irritation, especially on the back of hands and wrists. Protective clothing or the use of barrier skin creams is recommended for people in an area where carbon fiber dust is present. The sizing materials used to coat the fibers often contain chemicals that can cause severe skin reactions, which also requires protection.
In addition to being strong, carbon fibers are also good conductors of electricity. As a result, carbon fiber dust can cause arcing and shorts in electrical equipment. If electrical equipment cannot be relocated from the area where carbon dust is present, the equipment is sealed in a cabinet or other enclosure.
The Future
The latest development in carbon fiber technology is tiny carbon tubes called nanotubes.
These hollow tubes, some as small as 0.00004 in (0.001 mm) in diameter, have unique mechanical and electrical properties that may be useful in making new high-strength fibers, submicroscopic test tubes, or possibly new semiconductor materials for integrated circuits.
Where to Learn More
Books
Brady, George S., Henry R. Clauser, and John A. Vaccari. Materials Handbook. McGraw-Hill, 1997.
Kroschwitz, Jacqueline I. and Mary Howe-Grant, ed. Encyclopedia of Chemical Technology. John Wiley and Sons, Inc., 1993.
Periodicals
Ebbesen, T.W. "Carbon Nanotubes." Physics Today (June 1996): 26-32.
Other
American Carbon Society website. www.americancarbonsociety.org
Carbon Composites website. http://www.carb.com.
[Article by: Chris Cavette]
Wikipedia:
Carbon fiber |
This article is about loose or woven carbon filament. For the rigid composite material made from carbon fiber, see Carbon fiber reinforced plastic.
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This article needs references that appear in reliable third-party publications. Primary sources or sources affiliated with the subject are generally not sufficient for a Wikipedia article. Please add more appropriate citations from reliable sources. (March 2009) |
Carbon fiber (carbon fibre), alternatively graphite fiber, carbon graphite or CF, is a material consisting of extremely thin fibers about 0.005–0.010 mm in diameter and composed mostly of carbon atoms. The carbon atoms are bonded together in microscopic crystals that are more or less aligned parallel to the long axis of the fiber. The crystal alignment makes the fiber very strong for its size. Several thousand carbon fibers are twisted together to form a yarn, which may be used by itself or woven into a fabric.[1] Carbon fiber has many different weave patterns and can be combined with a plastic resin and wound or molded to form composite materials such as carbon fiber reinforced plastic (also referenced as carbon fiber) to provide a high strength-to-weight ratio material. The density of carbon fiber is also considerably lower than the density of steel, making it ideal for applications requiring low weight.[2] The properties of carbon fiber such as high tensile strength, low weight, and low thermal expansion make it very popular in aerospace, civil engineering, military, and motorsports, along with other competition sports. However, it is relatively expensive when compared to similar materials such as fiberglass or plastic. Carbon fiber is very strong when stretched or bent, but weak when compressed or exposed to high shock (eg. a carbon fiber bar is extremely difficult to bend, but will crack easily if hit with a hammer).
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Contents
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History of carbon fiber
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This section needs additional citations for verification. Please help improve this article by adding reliable references. Unsourced material may be challenged and removed. (November 2009) |
In 1958, Dr. Roger Bacon created high-performance carbon fibers at the Union Carbide Parma Technical Center, located outside of Cleveland, Ohio.[3] Those fibers were manufactured by heating strands of rayon until they carbonized. This process proved to be inefficient, as the resulting fibers contained only about 20% carbon and had low strength and stiffness properties. In the early 1960s, a process was developed using polyacrylonitrile (PAN) as a raw material. This had produced a carbon fiber that contained about 55% carbon and had much better properties. The polyacrylonitrile (PAN) conversion process quickly became the primary method for producing carbon fibers.[1]
The high potential strength of carbon fiber was realized in 1963 in a process developed at the Royal Aircraft Establishment at Farnborough, Hampshire. The process was patented by the Ministry of Defence and then licensed by the NRDC to three British companies: Rolls-Royce, already making carbon fiber, Morganite and Courtaulds. They were able to establish industrial carbon fiber production facilities within a few years, and Rolls-Royce took advantage of the new material's properties to break into the American market with its RB-211 aero-engine.
Even then, though, there was public concern over the ability of British industry to make the best of this breakthrough. In 1969 a House of Commons select committee inquiry into carbon fiber prophetically asked: "How then is the nation to reap the maximum benefit without it becoming yet another British invention to be exploited more successfully overseas?" Ultimately, this concern was justified. One by one the licensees pulled out of carbon-fiber manufacture. Rolls-Royce's interest was in state-of-the-art aero-engine applications. Its own production process was to enable it to be leader in the use of carbon-fiber reinforced plastics. In-house production would typically cease once reliable commercial sources became available.
Unfortunately, Rolls-Royce pushed the state-of-the-art too far, too quickly, in using carbon fiber in the engine's compressor blades, which proved vulnerable to damage from bird impact. What seemed a great British technological triumph in 1968 quickly became a disaster as Rolls-Royce's ambitious schedule for the RB-211 was endangered. Indeed, Rolls-Royce's problems became so great that the company was eventually nationalized by Edward Heath's Conservative government in 1971 and the carbon-fiber production plant sold off to form Bristol Composites.
Given the limited market for a very expensive product of variable quality, Morganite also decided that carbon-fiber production was peripheral to its core business, leaving Courtaulds as the only big UK manufacturer.
The company continued making carbon fiber, developing two main markets: aerospace and sports equipment. The speed of production and the quality of the product were improved.
Continuing collaboration with the staff at Farnborough proved helpful in the quest for higher quality, but, ironically, Courtaulds's big advantage as manufacturer of the "Courtelle" precursor now became a weakness. Low cost and ready availability were potential advantages, but the water-based inorganic process used to produce Courtelle made it susceptible to impurities that did not affect the organic process used by other carbon-fiber manufacturers.
Nevertheless, during the 1980s Courtaulds continued to be a major supplier of carbon fiber for the sports-goodsmarket, with Mitsubishi its main customer. But a move to expand, including building a production plant in California, turned out badly. The investment did not generate the anticipated returns, leading to a decision to pull out of the area. Courtaulds ceased carbon-fiber production in 1991, though ironically the one surviving UK carbon-fiber manufacturer continued to thrive making fiber based on Courtaulds's precursor. Inverness-based RK Carbon Fibres Ltd has concentrated on producing carbon fiber for industrial applications, and thus does not need to compete at the quality levels reached by overseas manufacturers.
During the 1970s, experimental work to find alternative raw materials led to the introduction of carbon fibers made from a petroleum pitch derived from oil processing. These fibers contained about 85% carbon and had excellent flexural strength.[1]
Structure and properties
Carbon fibers are the closest to asbestos in a number of properties.[4] Each carbon filament thread is a bundle of many thousand carbon filaments. A single such filament is a thin tube with a diameter of 5–8 micrometers and consists almost exclusively of carbon. The earliest generation of carbon fibers (i.e., T300, and AS4) had diameters of 7-8 micrometers[5]. Later fibers (i.e., IM6) have diameters that are approximately 5 micrometers[5].
The atomic structure of carbon fiber is similar to that of graphite, consisting of sheets of carbon atoms (graphene sheets) arranged in a regular hexagonal pattern. The difference lies in the way these sheets interlock. Graphite is a crystalline material in which the sheets are stacked parallel to one another in regular fashion. The intermolecular forces between the sheets are relatively weak Van der Waals forces, giving graphite its soft and brittle characteristics. Depending upon the precursor to make the fiber, carbon fiber may be turbostratic or graphitic, or have a hybrid structure with both graphitic and turbostratic parts present. In turbostratic carbon fiber the sheets of carbon atoms are haphazardly folded, or crumpled, together. Carbon fibers derived from Polyacrylonitrile (PAN) are turbostratic, whereas carbon fibers derived from mesophase pitch are graphitic after heat treatment at temperatures exceeding 2200 C. Turbostratic carbon fibers tend to have high tensile strength, whereas heat-treated mesophase-pitch-derived carbon fibers have high Young's modulus and high thermal conductivity.
Applications
For common applications, see Carbon fiber reinforced polymer.
Carbon fiber is most notably used to reinforce composite materials, particularly the class of materials known as Carbon fiber or graphite reinforced polymers. Non-polymer materials can also be used as the matrix for carbon fibers. Due to the formation of metal carbides and corrosion considerations, carbon has seen limited success in metal matrix composite applications. Reinforced carbon-carbon (RCC) consists of carbon fiber-reinforced graphite, and is used structurally in high-temperature applications. The fiber also finds use in filtration of high-temperature gasses, as an electrode with high surface area and impeccable corrosion resistance, and as an anti-static component. Molding a thin layer of carbon fibers significantly improves fire resistance of polymers or thermoset composites because a dense, compact layer of carbon fibers efficiently reflects heat.[6].
It has also been used in experimental medical procedures to treat severe burns. Brian Eno underwent extensive surgery in early 2009 which complemented a regular skin graft on his arm with carbon fiber threads. Being carbon based, doctors were able to fuse together his skin cells with the carbon fiber.[7]
Most recently, it has been used in Helios braces, braces for Charcot Marie Tooth and other Peripheral neuropathy patients
Synthesis
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This section does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (November 2009) |
Each carbon filament is made out of long, thin filaments of carbon sometimes transformed to graphite. A common method of making carbon filaments is the oxidation and thermal pyrolysis of polyacrylonitrile (PAN), a polymer based on acrylonitrile used in the creation of synthetic materials. Like all polymers, polyacrylonitrile molecules are long chains, which are aligned in the process of drawing continuous filaments. A common method of manufacture involves heating the PAN to approximately 300 °C in air, which breaks many of the hydrogen bonds and oxidizes the material. The oxidized PAN is then placed into a furnace having an inert atmosphere of a gas such as argon, and heated to approximately 2000 °C, which induces graphitization of the material, changing the molecular bond structure. When heated in the correct conditions, these chains bond side-to-side (ladder polymers), forming narrow graphene sheets which eventually merge to form a single, columnar filament. The result is usually 93–95% carbon. Lower-quality fiber can be manufactured using pitch or rayon as the precursor instead of PAN. The carbon can become further enhanced, as high modulus, or high strength carbon, by heat treatment processes. Carbon heated in the range of 1500-2000 °C (carbonization) exhibits the highest tensile strength (820,000 psi or 5,650 MPa or 5,650 N/mm²), while carbon fiber heated from 2500 to 3000 °C (graphitizing) exhibits a higher modulus of elasticity (77,000,000 psi or 531 GPa or 531 kN/mm²).
Textile
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This section does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (November 2009) |
Precursors for carbon fibers are polyacrylonitrile (PAN), rayon and pitch. Carbon fiber filament yarns are used in several processing techniques: the direct uses are for prepregging, filament winding, pultrusion, weaving, braiding, etc. Carbon fiber yarn is rated by the linear density (weight per unit length, i.e. 1 g/1000 m = 1 tex) or by number of filaments per yarn count, in thousands. For example, 200 tex for 3,000 filaments of carbon fiber is three times as strong as 1,000 carbon fibers, but is also three times as heavy. This thread can then be used to weave a carbon fiber filament fabric or cloth. The appearance of this fabric generally depends on the linear density of the yarn and the weave chosen. Some commonly used types of weave are twill, satin and plain.
Manufacturers
- PAN aerospace/high end carbon fiber
- Toray Industries (largest worldwide manufacturer)[citation needed]
- Toho Tenax
- Mitsubishi Rayon
- Hexcel
- Cytec Industries
- Schunk Gruppe
- PAN commercial grade carbon fiber
- Zoltek[2]
- SGL Carbon
- Fortafil
- Pitch carbon fiber
- Sumitomo
- Kureha Corporation
See also
References
- ^ a b c carbon fiber: Definition and Much More from Answers.com
- ^ Mr. Jeremy Hierholzer, Assistant Professor of Aviation Technology, Purdue University, 2007.
- ^ Bacon's breakthrough
- ^ Properties And Fiber Types
- ^ a b W.J. Cantwell, J Morton (1991). "The impact resistance of composite materials -- a review". Composites 22 (5): 347–62. doi:.
- ^ Z. Zhao and J. Gou "Improved fire retardancy of thermoset composites modified with carbon nanofibers" Sci. Technol. Adv. Mater. 10 (2009) 015005 free download
- ^ [1]Interview with Sydney University Radio Group, 18th of May 2009
External links
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Wikimedia Commons has media related to: Carbon fibres |
- Bacon's breakthrough at ACS.org
- Carbon Fiber at ps
- The Chemistry of Carbon Fiber
- Making Carbon Fiber
- Process instrumentation
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