Diamond is one of the best known allotropes of carbon, whose hardness and high dispersion of light make it useful for industrial applications and jewelry. Diamond is the hardest known natural mineral, which makes it an excellent abrasive and makes it hold polish and luster extremely well. No known naturally occurring substance can scratch, let alone cut, a diamond.
The market for industrial-grade diamonds operates much differently from its gem-grade counterpart. Industrial diamonds are valued mostly for their hardness and heat conductivity, making many of the gemological characteristics of diamond, including clarity and color, mostly irrelevant. This helps explain why 80% of mined diamonds (equal to about 100 million carats or 20,000 kg annually), unsuitable for use as gemstones and known as bort, are destined for industrial use. In addition to mined diamonds, synthetic diamonds found industrial applications almost immediately after their invention in the 1950s; another 400 million carats (80,000 kg) of synthetic diamonds are produced annually for industrial use—nearly four times the mass of natural diamonds mined over the same period.
The dominant industrial use of diamond is in cutting, drilling (drill bits), grinding (diamond edged cutters), and polishing. Most uses of diamonds in these technologies do not require large diamonds; in fact, most diamonds that are gem-quality can find an industrial use. Diamonds are embedded in drill tips or saw blades, or ground into a powder for use in grinding and polishing applications. Specialized applications include use in laboratories as containment for high pressure experiments (see diamond anvil), high-performance bearings, and limited use in specialized windows.
With the continuing advances being made in the production of synthetic diamond, future applications are beginning to become feasible. Garnering much excitement is the possible use of diamond as a semiconductor suitable to build microchips from, or the use of diamond as a heat sink in electronics. Significant research efforts in Japan, Europe, and the United States are under way to capitalize on the potential offered by diamond's unique material properties, combined with increased quality and quantity of supply starting to become available from synthetic diamond manufacturers.
Each carbon atom in a diamond is covalently bonded to four other carbons in a tetrahedron. These tetrahedrons together form a 3-dimensional network of puckered six-membered rings of atoms. This stable network of covalent bonds and the three dimensional arrangement of bonds is the reason that diamond is so strong.
Graphite is able to conduct electricity, due to delocalization of the pi bond electrons above and below the planes of the carbon atoms. These electrons are free to move, so are able to conduct electricity. However, the electricity is only conducted along the plane of the layers. In diamond all four outer electrons of each carbon atom are 'localised' between the atoms in covalent bonding. The movement of electrons is restricted and diamond does not conduct an electric current. In graphite, each carbon atom uses only 3 of its 4 outer energy level electrons in covalently bonding to three other carbon atoms in a plane. Each carbon atom contributes one electron to a delocalised system of electrons that is also a part of the chemical bonding. The delocalised electrons are free to move throughout the plane. For this reason, graphite conducts electricity along the planes of carbon atoms, but does not conduct in a direction at right angles to the plane.
Graphite powder is used as a dry lubricant. Although it might be thought that this industrially important property is due entirely to the loose interlamellar coupling between sheets in the structure, in fact in a vacuum environment (such as in technologies for use in space), graphite was found to be a very poor lubricant. This fact led to the discovery that graphite's lubricity is due to adsorbed air and water between the layers, unlike other layered dry lubricants such as molybdenum disulfide. Recent studies suggest that an effect called superlubricity can also account for this effect.
When a large number of crystallographic defects bind these planes together, graphite loses its lubrication properties and becomes what is known as pyrolytic carbon, a useful material in blood-contacting implants such as prosthetic heart valves.
Natural and crystalline graphites are not often used in pure form as structural materials due to their shear-planes, brittleness and inconsistent mechanical properties.
In its pure glassy (isotropic) synthetic forms, pyrolytic graphite and carbon fiber graphite is an extremely strong, heat-resistant (to 3000 °C) material, used in reentry shields for missile nosecones, solid rocket engines, high temperature reactors, brake shoes and electric motor brushes.
Intumescent or expandable graphites are used in fire seals, fitted around the perimeter of a fire door. During a fire the graphite intumesces (expands and chars) to resist fire penetration and prevent the spread of fumes. A typical start expansion temperature (SET) is between 150 and 300 degrees Celsius.
Density: its specific gravity is 2.3 which makes it lighter than diamond.
Effect of heat: it is the most stable allotrope of carbon. At a temperature of 2500 degree Celsius, it can be transformed into diamond. At about 700 degree Celsius it burns in pure oxygen forming carbon dioxide.
Chemical activity: it is slightly more reactive than diamond. This is because the reactants are able to penetrate between the hexagonal layers of carbon atoms in graphite. It is unaffected by ordinary solvents, dilute acids, or fused alkalis. However, chromic acid oxidises it to carbon dioxide.
While entirely amorphous carbon can be made, natural amorphous carbon (such as soot) actually contains microscopic crystals of graphite, sometimes diamond On the macroscopic scale, amorphous carbon has no definite structure as it conisists of small irregular cystals, but on the nanomicroscopic scale, we can see it is made of regularly arranged carbon atoms.
Coal and soot are both informally called amorphous carbon. However, both are products of pyrolysis (the process of decomposing a substance by the action of heat), which does not produce true amorphous carbon under normal conditions. The coal industry divides coal up into various grades depending on the amount of carbon present in the sample compared to the amount of impurities. The highest grade, anthracite, is about 90 percent carbon and 10% other elements. Bituminous coal is about 75-90 percent carbon, and lignite is the name for coal that is around 55 percent carbon.
As of the early twenty-first century, the chemical and physical properties of fullerenes are still under heavy study, in both pure and applied research labs. In April 2003, fullerenes were under study for potential medicinal use — binding specific antibiotics to the structure to target resistant bacteria and even target certain cancer cells such as melanoma.
Carbon nanotubes, also called buckytubes, are cylindrical carbon molecules with novel properties that make them potentially useful in a wide variety of applications (e.g., nano-electronics, optics, materials applications, etc.). They exhibit extraordinary strength, unique electrical properties, and are efficient conductors of heat. Inorganic nanotubes have also been synthesized. A nanotube (also known as a buckytube) is a member of the fullerene structural family, which also includes buckyballs. Whereas buckyballs are spherical in shape, a nanotube is cylindrical, with at least one end typically capped with a hemisphere of the buckyball structure. Their name is derived from their size, since the diameter of a nanotube is on the order of a few nanometers (approximately 50,000 times smaller than the width of a human hair), while they can be up to several centimeters in length. There are two main types of nanotubes: single-walled nanotubes (SWNTs) and multi-walled nanotubes (MWNTs).
Carbon NanoBuds are a newly discovered allotrope of carbon in which fullerene like "buds" are covalently attached to the outer sidewalls of the carbon nanotubes. This hybrid material has useful properties of both fullerenes and carbon nanotubes. In particular, they have been found to be exceptionally good field emitters.
It was first produced by Bernard Redfern in the mid 1950's at the laboratories of The Carborundum Company, Trafford Park, Manchester, UK. He set out to develop a polymer matrix to mirror a diamond structure and discovered a resole (phenolic) resin that would, with special preparation, set without a catalyst. Using this resin the first glassy carbon was produced. Patents were filed some of which were withdrawn in the interests of national security. Original research samples of resin and product exist.
The preparation of glassy carbon involves subjecting the organic precursors to a series of heat treatments at temperatures up to 3000oC. Unlike many non-graphitizing carbons, they are impermeable to gases and are chemically extremely inert, especially those which have been prepared at very high temperatures. It has been demonstrated that the rates of oxidation of certain glassy carbons in oxygen, carbon dioxide or water vapour are lower than those of any other carbon. They are also highly resistant to attack by acids. Thus, while normal graphite is reduced to a powder by a mixture of concentrated sulfuric and nitric acids at room temperature, glassy carbon is unaffected by such treatment, even after several months.
Each cluster is about 6 nanometers wide and consists of about 4000 carbon atoms linked in graphite-like sheets that are given negative curvature by the inclusion of heptagons among the regular hexagonal pattern. This is the opposite of what happens in the case of buckminsterfullerenes, in which carbon sheets are given positive curvature by the inclusion of pentagons.
The large-scale structure of carbon nanofoam is similar to that of an aerogel, but with 1% of the density of previously produced carbon aerogels - only a few times the density of air at sea level. Unlike carbon aerogels, carbon nanofoam is a poor electrical conductor.
Lonsdaleite was first identified from the Canyon Diablo meteorite at Barringer Crater (also known as Meteor Crater) in Arizona. It was first discovered in 1967. Lonsdaleite occurs as microscopic crystals associated with diamond in the Canyon Diablo meteorite; Kenna meteorite, New Mexico; and Allan Hills (ALH) 77283, Victoria Land, Antarctica meteorite. It has also been reported from the Tunguska impact site, Russia.
The same polymer was synthesized in early 1960s by group of Soviet chemists and was called carbyne (Russian: карбин). It appeared to be a semiconductor that is very sensitive to light, thus it was suggested to use it in photodiodes and similar devices.
Carbyne, or polyyne, is also another name for Linear Acetylenic Carbon (LAC) the carbon allotrope that has the chemical structure -(C:::C)n- .Carbon in this modification is linear with sp orbital hybridisation, and is a polymer with alternating single and triple bonds. This type of carbyne is of considerable interest to nanotechnology as its Young's modulus is forty times that of diamond .
The system of carbon allotropes spans an astounding range of extremes, considering that they are all merely structural formations of the same element.
Between diamond and graphite: