Diamond
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Diamond one of the forms of carbon
Diamond is one of the two best known forms (or allotropes) of
carbon, whose hardness and high dispersion of light make it useful
for industrial applications and jewelry (the other equally well
known allotrope is graphite). Diamonds are specifically renowned as
a mineral with superlative physical qualities - they make excellent
abrasives because they can only be scratched by other diamonds,
which also means they hold a polish extremely well and retain
luster. About 130 million carats (26,000 kg) are mined annually,
with a total value of nearly USD $9 billion.
The name "diamond" derives from the ancient Greek adamas (αδάμας;
"invincible"). They have been treasured as gems since their use as
religious icons in India at least 2,500 years ago—and usage in drill
bits and engraving tools also dates to early human history.
Popularity of diamonds has risen since the 19th century because of
increased supply, improved cutting and polishing techniques, and
growth in the world economy.
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They are commonly judged by the "four Cs": carat, clarity, color,
and cut. Although nearly four times the mass of natural diamonds are
produced as synthetic diamond each year, the vast majority of
synthetic diamond production remains small, imperfect diamonds
suitable only for industrial-grade use.
Most natural diamonds originate from central and southern Africa,
although significant sources of the mineral have been discovered in
Canada, India, Russia, Brazil, and Australia. They are generally
mined from volcanic pipes, which are deep in the Earth where the
high pressure and temperature enables the formation of the crystals.
The mining and distribution of natural diamonds are subjects of
frequent controversy—such as with concerns over the sale of conflict
diamonds by African paramilitary groups. There are also allegations
that the De Beers Group misuses its dominance in the industry to
control supply and manipulate price via monopolistic practices,
although in recent years the company's market share has dropped to
below 50%.
Diamond is a transparent crystal of pure carbon consisting of
tetrahedrally bonded carbon atoms. Humans have been able to adapt
diamonds for many uses because of the material's exceptional
physical characteristics. Most notable among these properties are
the extreme hardness of diamond, its high dispersion index, and high
thermal conductivity. These properties form the basis for most
modern applications of diamond.
Diamonds typically crystallize in the face-centered cubic crystal
system and consist of tetrahedrally bonded carbon atoms. The unit
cell of diamond has a two atom basis at (0,0,0) and (1/4,1/4,1/4),
which means half of the atoms are at lattice points and the other
half are offset by (1/4,1/4,1/4), where 1 is the length of a side of
the unit cell.
The tetrahedral arrangement of atoms in a diamond crystal is the
source of many of diamond's properties. Graphite, another allotrope
of carbon, has a rhombohedra crystal structure and as a result shows
dramatically different physical characteristics — contrary to
diamond, graphite is a very soft, dark gray, opaque mineral. Other
elements of the carbon group such as silicon have forms analogous to
diamond.
Lonsdaleite is a polymorph of diamond (and a distinct mineral
species) that crystallizes with hexagonal symmetry; it is rarely
found in nature, but is characteristic of synthetic diamonds. A
cryptocrystalline variety of diamond is called carbonado. A
colorless, grey or black diamond with a tiny radial structure is a
spherulite.
Diamond is the hardest known naturally occurring material, scoring
10 on the relative Mohs scale of mineral hardness and having an
absolute hardness value of between 167 and 231 gigapascals in
various tests. Diamond's hardness has been known since antiquity,
and is the source of its name. However, aggregated diamond nanorods,
an allotrope of carbon first synthesized in 2005, are now believed
to be even harder than diamond.
The hardest diamonds in the world are diamonds from the New England
area in New South Wales, Australia. These diamonds are generally
small, perfect to semi perfect octahedral, and are used to polish
other diamonds. Their hardness is considered to be a product of the
crystal growth form, which is single stage growth crystal. Most
other diamonds show more evidence of multiple growth stages, which
produce inclusions, flaws and defect planes in the crystal lattice
all of which affect their hardness (Taylor et al. 1990).
Industrial use of diamonds has historically been associated with
their hardness; this property makes diamond the ideal material for
cutting and grinding tools. It is one of the most known and most
useful of more than 3,000 known minerals. As the hardest known
naturally occurring material, diamond can be used to polish, cut, or
wear away any material, including other diamonds. Common industrial
adaptations of this ability include diamond-tipped drill bits and
saws, or use of diamond powder as an abrasive. Other specialized
applications also exist or are being developed, including use as
semiconductors: some blue diamonds are natural semiconductors, in
contrast to most other diamonds, which are excellent electrical
insulators. Industrial-grade diamonds are either unsuitable for use
as gems or synthetically produced, which lowers their price and
makes their use economically feasible. Industrial applications,
especially as drill bits and engraving tools, also date to ancient
times.
The hardness of diamonds also contributes to its suitability as a
gemstone. Because it can only be scratched by other diamonds, it
maintains its polish extremely well, keeping its luster over long
periods of time. Unlike many other gems, it is well-suited to daily
wear because of its resistance to scratching—perhaps contributing to
its popularity as the preferred gem in an engagement ring or wedding
ring, which are often worn every day.
Unlike hardness, which only denotes resistance to scratching,
diamond's toughness is only fair to good. Toughness relates to a
material's ability to resist breakage from forceful impact. As with
any material, the macroscopic geometry of a diamond contributes to
its resistance to breakage. Diamond is therefore more fragile in
some orientations than others.
Diamonds occur in a variety of transparent hues — colorless, white,
steel, blue, yellow, orange, red, green, pink, brown—or colored
black. Diamonds with a detectable hue to them are known as colored
diamonds. If the color is strong enough, a stone may be referred to
as a fancy colored diamond by the trade. Colored diamonds contain
impurities or structural defects that cause the coloration, while
pure or nearly pure diamonds are transparent and colorless. Most
diamond impurities replace a carbon atom in the crystal lattice. The
most common impurity, nitrogen, causes a slight to strong yellow
coloration depending upon the type and concentration of nitrogen
present.
At surface air pressure (one atmosphere), diamonds are not as stable
as graphite, and so the decay of diamond is thermodynamically
favorable (ΔG = −2.99 kJ / mol). Diamonds will burn at approximately
800 degrees Celsius, providing that enough oxygen is available. This
was shown in the late 18th century, and previously described during
Roman times. However, owing to a very large kinetic energy barrier,
diamonds are metastable; under normal conditions, it would take an
extremely long time (possibly more than the age of the Universe) for
diamond to decay into graphite.
Diamonds exhibit a high dispersion of visible light. This strong
ability to split white light into its component colors is an
important aspect of diamond's attraction as a gemstone, giving it
impressive prismatic action that results in so-called fire in a
well-cut stone. The luster of a diamond, a characterization of how
light interacts with the surface of a crystal, is brilliant and is
described as adamantine, which simply means diamond-like. This is
owed to their high refractive index of 2.417 (at 589.3 nm), which
causes total internal reflection to occur. Some diamonds exhibit
fluorescence of various colors (predominately blue) under long wave
ultraviolet light. Nearly all diamonds fluoresce bluish-white,
yellow or green under X-rays and this property is used extensively
in mining to separate the fluorescing diamond from the
non-fluorescing rock. Most diamonds show no fluorescence although
colored diamonds show a wider range of fluorescence than the blue
fluorescence normally observed in clear diamonds.
Except for most blue diamonds, which are semiconductors, diamonds
are good electrical insulators. Blue diamonds owe their semi
conductive property to boron impurities, which act as a doping agent
and cause p-type semiconductor behavior. Blue diamonds which are not
boron-doped, such as those recently recovered from the Argyle
diamond mine in Australia that owe their color to an overabundance
of hydrogen atoms, are not semiconductors.
Unlike most electrical insulators, diamond is a good conductor of
heat because of the strong covalent bonding within the crystal. Most
natural blue diamonds contain boron atoms which replace carbon atoms
in the crystal matrix, and also have high thermal conductivity.
Specially purified synthetic diamond has the highest thermal
conductivity (2000–2500 W/(m·K), five times more than copper) of any
known solid at room temperature. Because diamond has such high
thermal conductance it is already used in semiconductor manufacture
to prevent silicon and other semi conducting materials from
overheating.
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