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From Wikipedia, the free encyclopedia
This article is about the mineral. For the gemstone, see Diamond (gemstone). For other uses, including the shape , see Diamond (disambiguation).
A clear octahedral stone protrudes from a black rock.
The slightly misshapen octahedral shape of this rough diamond crystal in matrix is typical of the mineral. Its lustrous faces also indicate that this crystal is from a primary deposit.
Category Native Minerals
(repeating unit)
Strunz classification 01.CB.10a
Formula mass 12.01 g⋅mol−1
Color Typically yellow, brown or gray to colorless. Less often blue, green, black, translucent white, pink, violet, orange, purple and red.
Crystal habit Octahedral
Crystal system Isometric-Hexoctahedral (Cubic)
Cleavage 111 (perfect in four directions)
Fracture Conchoidal (shell-like)
Mohs scalehardness 10
Luster Adamantine
Streak Colorless
Diaphaneity Transparent to subtransparent to translucent
Specific gravity 3.52±0.01
Density 3.5–3.53 g/cm3
Polish luster Adamantine
Optical properties Isotropic
Refractive index 2.418 (at 500 nm)
Birefringence None
Pleochroism None
Dispersion 0.044
Melting point Pressure dependent
References [1][2]

In mineralogydiamond (from the ancient Greek αδ?μας – adámas "unbreakable") is a metastable allotrope of carbon, where the carbon atoms are arranged in a variation of the face-centered cubic crystal structure called a diamond lattice. Diamond is less stable than graphite, but the conversion rate from diamond to graphite is negligible at standard conditions. Diamond is renowned as a material with superlative physical qualities, most of which originate from the strong covalent bonding between its atoms. In particular, diamond has the highest hardness and thermal conductivity of any bulk material. Those properties determine the major industrialapplication of diamond in cutting and polishing tools and the scientific applications in diamond knives and diamond anvil cells.

Because of its extremely rigid lattice, it can be contaminated by very few types of impurities, such as boron and nitrogen. Small amounts of defects or impurities (about one per million of lattice atoms) color diamond blue (boron), yellow (nitrogen), brown (lattice defects), green (radiation exposure), purple, pink, orange or red. Diamond also has relatively high optical dispersion (ability to disperse light of different colors).

Most natural diamonds are formed at high temperature and pressure at depths of 140 to 190 kilometers (87 to 118 mi) in the Earth's mantle. Carbon-containing minerals provide the carbon source, and the growth occurs over periods from 1 billion to 3.3 billion years (25% to 75% of the age of the Earth). Diamonds are brought close to the Earth′s surface through deep volcanic eruptions by a magma, which cools into igneous rocks known as kimberlites and lamproites. Diamonds can also be produced synthetically in a high-pressure high-temperature process which approximately simulates the conditions in the Earth's mantle. An alternative, and completely different growth technique is chemical vapor deposition (CVD). Several non-diamond materials, which include cubic zirconia and silicon carbide and are often called diamond simulants, resemble diamond in appearance and many properties. Special gemological techniques have been developed to distinguish natural and synthetic diamonds and diamond simulants.




The name diamond is derived from the ancient Greek αδ?μας (adámas), "proper", "unalterable", "unbreakable", "untamed", from ?- (a-), "un-" + δαμ?ω (damá?), "I overpower", "I tame".[3] Diamonds are thought to have been first recognized and mined in India, where significant alluvial deposits of the stone could be found many centuries ago along the rivers PennerKrishna and Godavari. Diamonds have been known in India for at least 3,000 years but most likely 6,000 years.[4]

Diamonds have been treasured as gemstones since their use as religious icons in ancient India. Their usage in engraving tools also dates to early human history.[5][6] The popularity of diamonds has risen since the 19th century because of increased supply, improved cutting and polishing techniques, growth in the world economy, and innovative and successful advertising campaigns.[7]

In 1772, Antoine Lavoisier used a lens to concentrate the rays of the sun on a diamond in an atmosphere of oxygen, and showed that the only product of the combustion was carbon dioxide, proving that diamond is composed of carbon.[8] Later in 1797, Smithson Tennant repeated and expanded that experiment.[9] By demonstrating that burning diamond and graphite releases the same amount of gas he established the chemical equivalence of these substances.[10]

The most familiar use of diamonds today is as gemstones used for adornment, a use which dates back into antiquity. The dispersion of white light into spectral colors is the primary gemological characteristic of gem diamonds. In the 20th century, experts in gemology have developed methods of grading diamonds and other gemstones based on the characteristics most important to their value as a gem. Four characteristics, known informally as the four Cs, are now commonly used as the basic descriptors of diamonds: these are caratcutcolor, and clarity.[11] A large, flawless diamond is known as a paragon.

Natural history

The formation of natural diamond requires very specific conditions—exposure of carbon-bearing materials to high pressure, ranging approximately between 45 and 60 kilobars (4.5 and 6 GPa), but at a comparatively low temperature range between approximately 900 and 1,300 °C (1,650 and 2,370 °F). These conditions are met in two places on Earth; in the lithospheric mantle below relatively stable continental plates, and at the site of a meteorite strike.[12]

Formation in cratons

A triangular facet of a crystal having triangular etch pits with the largest having a base length of about 0.2 millimetres (0.0079 in)
One face of an uncut octahedral diamond, showing trigons (of positive and negative relief) formed by natural chemical etching

The conditions for diamond formation to happen in the lithospheric mantle occur at considerable depth corresponding to the requirements of temperature and pressure. These depths are estimated between 140 and 190 kilometers (87 and 118 mi) though occasionally diamonds have crystallized at depths about 300 kilometers (190 mi).[13] The rate at which temperature changes with increasing depth into the Earth varies greatly in different parts of the Earth. In particular, under oceanic plates the temperature rises more quickly with depth, beyond the range required for diamond formation at the depth required. The correct combination of temperature and pressure is only found in the thick, ancient, and stable parts of continental plates where regions of lithosphere known as cratons exist. Long residence in the cratonic lithosphere allows diamond crystals to grow larger.[13]

Through studies of carbon isotope ratios (similar to the methodology used in carbon dating, except with the stable isotopes C-12 and C-13), it has been shown that the carbon found in diamonds comes from both inorganic and organic sources. Some diamonds, known as harzburgitic, are formed from inorganic carbon originally found deep in the Earth's mantle. In contrast, eclogitic diamonds contain organic carbon from organic detritus that has been pushed down from the surface of the Earth's crust through subduction (see plate tectonics) before transforming into diamond. These two different source of carbon have measurably different 13C:12C ratios. Diamonds that have come to the Earth's surface are generally quite old, ranging from under 1 billion to 3.3 billion years old. This is 22% to 73% of the age of the Earth.[13]

Diamonds occur most often as euhedral or rounded octahedra and twinned octahedra known as macles. As diamond's crystal structure has a cubic arrangement of the atoms, they have many facets that belong to a cube, octahedron, rhombicosidodecahedrontetrakis hexahedron or disdyakis dodecahedron. The crystals can have rounded off and unexpressive edges and can be elongated. Sometimes they are found grown together or form double "twinned" crystals at the surfaces of the octahedron. These different shapes and habits of some diamonds result from differing external circumstances. Diamonds (especially those with rounded crystal faces) are commonly found coated in nyf, an opaque gum-like skin.[14]


Transport from mantle

Schematic cross section of an underground region 3 km deep and 2 km wide. A red dike stretches across the bottom, and a pipe containing some xenoliths runs from the dike to the surface, varying from red at the bottom to orange-yellow at the top. The pipe's root, at its bottom, is about 1 km long, and its diatreme, above the root, is about 1.5 km long. The pipe's top is a crater, rimmed by a tuff ring and containing washed-back ejecta. The erosion level is almost zero for Orapa, about 1 km for Jagersfontein, and about 1.4 km for Kimberley.
Schematic diagram of a volcanic pipe

Diamond-bearing rock is carried from the mantle to the Earth's surface by deep-origin volcanic eruptions. The magma for such a volcano must originate at a depth where diamonds can be formed[13]—150 km (93 mi) or more (three times or more the depth of source magma for most volcanoes). This is a relatively rare occurrence. These typically small surface volcanic craters extend downward in formations known as volcanic pipes.[13] The pipes contain material that was transported toward the surface by volcanic action, but was not ejected before the volcanic activity ceased. During eruption these pipes are open to the surface, resulting in open circulation; manyxenoliths of surface rock and even wood and fossils are found in volcanic pipes. Diamond-bearing volcanic pipes are closely related to the oldest, coolest regions of continental crust (cratons). This is because cratons are very thick, and their lithospheric mantle extends to great enough depth that diamonds are stable. Not all pipes contain diamonds, and even fewer contain enough diamonds to make mining economically viable.[13] Diamonds are very rare[22] because most of the crust is too thin to permit diamond crystallization, whereas most of the mantle has relatively little carbon.

The magma in volcanic pipes is usually one of two characteristic types, which cool into igneous rock known as either kimberlite or lamproite.[13] The magma itself does not contain diamond; instead, it acts as an elevator that carries deep-formed rocks (xenoliths), minerals (xenocrysts), and fluids upward. These rocks are characteristically rich in magnesium-bearing olivinepyroxene, and amphibole minerals[13] which are often altered to serpentineby heat and fluids during and after eruption. Certain indicator minerals typically occur within diamantiferous kimberlites and are used as mineralogical tracers by prospectors, who follow the indicator trail back to the volcanic pipe which may contain diamonds. These minerals are rich in chromium (Cr) or titanium (Ti), elements which impart bright colors to the minerals. The most common indicator minerals are chromium garnets (usually bright red chromium-pyrope, and occasionally green ugrandite-series garnets), eclogitic garnets, orange titanium-pyrope, red high-chromium spinels, dark chromite, bright green chromium-diopside, glassy green olivine, blackpicroilmenite, and magnetite. Kimberlite deposits are known as blue ground for the deeper serpentinized part of the deposits, or as yellow ground for the near surface smectite clay and carbonate weathered and oxidizedportion.[13]

Once diamonds have been transported to the surface by magma in a volcanic pipe, they may erode out and be distributed over a large area. A volcanic pipe containing diamonds is known as a primary source of diamonds. Secondary sources of diamonds include all areas where a significant number of diamonds have been eroded out of their kimberlite or lamproite matrix, and accumulated because of water or wind action. These include alluvial deposits and deposits along existing and ancient shorelines, where loose diamonds tend to accumulate because of their size and density. Diamonds have also rarely been found in deposits left behind by glaciers (notably in Wisconsin and Indiana); in contrast to alluvial deposits, glacial deposits are minor and are therefore not viable commercial sources of diamond.[13]



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