quarta-feira, 13 de janeiro de 2016

Chrysoberyl

Chrysoberyl

From Wikipedia, the free encyclopedia
Chrysoberyl
Chrysoberyl-282796.jpg
General
CategoryOxide minerals
Formula
(repeating unit)
BeAl2O4
Strunz classification04.BA.05
Crystal symmetryOrthorhombic 2/m2/m2/m dipyramidal
Unit cella = 5.481 Å, b = 9.415 Å, c = 4.428 Å; Z = 8
Identification
ColorVarious shades of green, yellow, brownish to greenish black, may be raspberry-red under incandescent light when chromian; colorless, pale shades of yellow, green, or red in transmitted light
Crystal habitCrystals tabular or short prismatic, prominently striated
Crystal systemOrthorhombic
TwinningContact and penetration twins common, often repeated forming rosette structures
CleavageDistinct on {110}, imperfect on {010}, poor on {001}
FractureConchoidal to uneven
TenacityBrittle
Mohs scalehardness8.5
LusterVitreous
StreakWhite
Specific gravity3.5–3.84
Optical propertiesBiaxial (+)
Refractive indexnα=1.745 nβ=1.748 nγ=1.754
PleochroismX = red; Y = yellow-orange; Z = emerald-green
2V angleMeasured: 70°
References[1][2][3]
Major varieties
AlexandriteColor change; green to red
CymophaneChatoyant
The mineral or gemstone chrysoberyl is an aluminate of beryllium with the formula BeAl2O4.[3] The name chrysoberyl is derived from the Greek words χρυσός chrysos and βήρυλλος beryllos, meaning "a gold-white spar". Despite the similarity of their names, chrysoberyl and beryl are two completely different gemstones, although they both contain beryllium. Chrysoberyl is the third-hardest frequently encountered natural gemstone and lies at 8.5 on the hardness scale, between corundum (9) and topaz (8).[4]
An interesting feature of its crystals are the cyclic twins called trillings. These twinned crystals have a hexagonal appearance, but are the result of a triplet of twins with each "twin" oriented at 120° to its neighbors and taking up 120° of the cyclic trilling. If only two of the three possible twin orientations are present, a "V"-shaped twin results.
Ordinary chrysoberyl is yellowish-green and transparent to translucent. When the mineral exhibits good pale green to yellow color and is transparent, then it is used as a gemstone. The three main varieties of chrysoberyl are: ordinary yellow-to-green chrysoberyl, cat's eye or cymophane, and alexandrite. Yellow-green chrysoberyl was referred to as "chrysolite" during the Victorian and Edwardian eras, which caused confusion since that name has also been used for the mineral olivine ("peridot" as a gemstone); that name is no longer used in the gemological nomenclature.
Alexandrite, a strongly pleochroic (trichroic) gem, will exhibit emerald green, red and orange-yellow colors depending on viewing direction in partially polarised light. However, its most distinctive property is that it also changes color in artificial (tungsten/halogen) light compared to daylight. The color change from red to green is due to strong absorption of light in a narrow yellow portion of the spectrum, while allowing large bands of more blue-green and red wavelengths to be transmitted. Which of these prevails to give the perceived hue depends on the spectral balance of the illumination. Fine-quality alexandrite has a green to bluish-green color in daylight (relatively blue illumination of high color temperature), changing to a red to purplish-red color in incandescent light (relatively yellow illumination).[5] However, fine-color material is extremely rare. Less-desirable stones may have daylight colors of yellowish-green and incandescent colors of brownish red.[5]
Cymophane is popularly known as "cat's eye". This variety exhibits pleasing chatoyancy or opalescence that reminds one of the eye of a cat. When cut to produce a cabochon, the mineral forms a light-green specimen with a silky band of light extending across the surface of the stone.

Occurrence[edit]

Chrysoberyl forms as a result of pegmatitic processes. Melting in the Earth's crust produces relatively low-density molten magmawhich can rise upwards towards the surface. As the main magma body cools, water originally present in low concentrations became more concentrated in the molten rock because it could not be incorporated into the crystallization of solid minerals. The remnant magma thus becomes richer in water, and also in rare elements that similarly do not fit in the crystal structures of major rock-forming minerals. The water extends the temperature range downwards before the magma becomes completely solid, allowing concentration of rare elements to proceed so far that they produce their own distinctive minerals. The resulting rock is igneous in appearance but formed at a low temperature from a water-rich melt, with large crystals of the common minerals such as quartz and feldspar, but also with elevated concentrations of rare elements such as beryllium, lithium, or niobium, often forming their own minerals; this is called apegmatite. The high water content of the magma made it possible for the crystals to grow quickly, so pegmatite crystals are often quite large, which increases the likelihood of gem specimens forming.
Chrysoberyl can also grow in the country rocks near to pegmatites, when Be- and Al-rich fluids from the pegmatite react with surrounding minerals. Hence, it can be found in mica schists and in contact with metamorphic deposits of dolomitic marble. Because it is a hard, dense mineral that is resistant to chemical alteration, it can be weathered out of rocks and deposited in river sands and gravels in alluvial deposits with other gem minerals such as diamond, corundum, topaz, spinel, garnet, and tourmaline. When found in such placers, it will have rounded edges instead of sharp, wedge-shape forms. Much of the chrysoberyl mined in Brazil and Sri Lanka is recovered from placers, as the host rocks have been intensely weathered and eroded.
If the pegmatite fluid is rich in beryllium, crystals of beryl or chrysoberyl could form. Beryl has a high ratio of beryllium to aluminium, while the opposite is true for chrysoberyl. Both are stable with the common mineral quartz. For alexandrite to form, some chromiumwould also have had to be present. However, beryllium and chromium do not tend to occur in the same types of rock. Chromium is commonest in mafic and ultramafic rocks in which beryllium is extremely rare. Beryllium becomes concentrated in felsic pegmatites in which chromium is almost absent. Therefore, the only situation where an alexandrite can grow is when Be-rich pegmatitic fluids react with Cr-rich country rock. This unusual requirement explains the rarity of this chrysoberyl variety.

Alexandrite[edit]

The alexandrite variety displays a color change (alexandrite effect) dependent upon the nature of ambient lighting. Alexandrite effect is the phenomenon of an observed color change from greenish to reddish with a change in source illumination.[6] Alexandrite results from small scale replacement of aluminium by chromium ions in the crystal structure, which causes intense absorption of light over a narrow range of wavelengths in the yellow region (580 nm) of the visible light spectrum.[6] Because human vision is more sensitive to light in the green spectrum and the red spectrum, alexandrite appears greenish in daylight where a full spectrum of visible light is present and reddish in incandescent light which emits less green and blue spectrum.[6] This color change is independent of any change of hue with viewing direction through the crystal that would arise frompleochroism.[6]
Alexandrite from the Ural Mountains in Russia can be green by daylight and red by incandescent light. Other varieties of alexandrite may be yellowish or pink in daylight and acolumbine or raspberry red by incandescent light.
Alexandrite step cut cushion, 26.75 cts.
Stones that show a dramatic color change and strong colors (e.g. red-to-green) are rare and sought-after,[5] but stones that show less distinct colors (e.g. yellowish green changing to brownish yellow) may also be considered alexandrite by gem labs such as the Gemological Institute of America.[7][8]
According to a popular but controversial story, alexandrite was discovered by the Finnish mineralogist Nils Gustaf Nordenskiöld (1792–1866), and named alexandrite in honor of the future Tsar Alexander II of Russia. Nordenskiöld's initial discovery occurred as a result of an examination of a newly found mineral sample he had received from Perovskii, which he identified as emerald at first.[9][10] The first emerald mine had been opened in 1831.
Alexandrite 5 carats (1,000 mg) and larger were traditionally thought to be found only in the Ural Mountains, but have since been found in larger sizes in Brazil. Other deposits are located in India (Andhra Pradesh), Madagascar, Tanzania and Sri Lanka. Alexandrite in sizes over three carats are very rare.
Today, several labs can produce synthetic lab-grown stones with the same chemical and physical properties as natural alexandrite. Several methods can produce flux-grown alexandrite, Czocchralski (or pulled) alexandrite, and hydrothermally-produced alexandrite. Flux-grown gems that are fairly difficult to distinguish from natural alexandrite as they contain inclusions that can look natural. Czochralski or pulled alexandrite is easier to identify because it is very clean and contains curved striations visible under magnification. Although the color change in pulled stones can be from blue to red, the color change does not truly resemble that of natural alexandrite from any deposit. Hydrothermal lab-grown alexandrite has identical physical and chemical properties to real alexandrite.[11]
Some gemstones falsely described as lab-grown synthetic alexandrite are actually corundum laced with trace elements (e.g., vanadium) or color-change spinel and are not actually chrysoberyl. As a result, they would be more accurately described as simulated alexandrite rather than synthetic. This alexandrite-like sapphire material has been around for almost 100 years and shows a characteristic purple-mauve colour change, which does not really look like alexandrite because there is never any green.[12]

Cymophane[edit]

Fine-color cymophane with a sharp and centered eye
Translucent yellowish chatoyant chrysoberyl is called cymophane or cat's eye. Cymophane has its derivation also from the Greek words meaning 'wave' and 'appearance', in reference to the haziness that visually distorts what would normally be viewed as a well defined surface of a cabochon. This effect may be combined with a cat eye effect. In this variety, microscopic tubelike cavities or needle-like inclusions [13] of rutile occur in an orientation parallel to the c-axis, producing a chatoyant effect visible as a single ray of light passing across the crystal. This effect is best seen in gemstones cut in cabochon form perpendicular to the c-axis. The color in yellow chrysoberyl is due to Fe3+ impurities.
Although other minerals such as tourmaline, scapolite, corundum, spinel and quartz can form "cat's eye" stones similar in appearance to cymophane, the jewelry industry designates these stones as "quartz cat's eyes", or "ruby cat's eyes" and only chrysoberyl can be referred to as "cat's eye" with no other designation.
Gems lacking the silky inclusions required to produce the cat's eye effect are usually faceted. An alexandrite cat's eye is a chrysoberyl cat's eye that changes color. "Milk and honey" is a term commonly used to describe the color of the best cat's eyes. The effect refers to the sharp milky ray of white light normally crossing the cabochon as a center line along its length and overlying the honey-colored background. The honey color is considered to be top-grade by many gemologists but the lemon yellow colors are also popular and attractive. Cat's eye material is found as a small percentage of the overall chrysoberyl production wherever chrysoberyl is found.
Cat's eye really became popular by the end of the 19th century when the Duke of Connaught gave a ring with a cat's eye as an engagement token; this was sufficient to make the stone more popular and increase its value greatly. Until that time, cat's eye had predominantly been present in gem and mineral collections. The increased demand in turn created an intensified search for it in Sri Lanka.[14]

Tanzanite

Tanzanite


Tanzanite
Zoïsite (Tanzanite).jpg
Tanzanite rough stone and cut stone
General
CategorySorosilicate
Formula
(repeating unit)
(Ca2Al3(SiO4)(Si2O7)O(OH)) + (Cr,Sr)
Strunz classification09.BG.10
Identification
ColorViolet, blue
Crystal habitPrismatic crystals with striations; massive to columnar[1][2]
Crystal systemOrthorhombic[1]
Twinningpenetration twins
CleavagePerfect {010}, imperfect {100}[1]
FractureUneven to conchoidal[1]
Mohs scalehardness6.5
LusterVitreous, pearly on cleavage surfaces
StreakWhite or colorless
Specific gravity3.10–3.38
Optical propertiesbiaxial positive
Refractive index1.69–1.70
Birefringence0.006–0.018
PleochroismPresent, dichroism or trichroismdepending on heat treatment.
Tanzanite is the blue/violet variety of the mineral zoisite (a calcium aluminium hydroxyl Sorosilicate) belonging to the epidote group. It was discovered in the Mererani Hills of Manyara Region in Northern Tanzania in 1967, near the city of Arusha and Mount Kilimanjaro. Tanzanite is used as a gemstone. Naturally formed tanzanite is extremely rare[3] and is endemic only to the Mererani Hills.[4]
Tanzanite is noted for its remarkably strong trichroism, appearing alternately sapphire blue, violet and burgundy depending oncrystal orientation.[5] Tanzanite can also appear differently when viewed under alternate lighting conditions. The blues appear more evident when subjected to fluorescent light and the violet hues can be seen readily when viewed under incandescent illumination. Tanzanite is usually a reddish brown in its rough state, requiring artificial heat treatment to bring out the blue violet of the stone.[6]
The mineral was named by Tiffany & Co. after Tanzania, the country in which it was discovered. In 2002, the American Gem Trade Association chose Tanzanite as a December birthstone, the first change to their birthstone list since 1912.[7]

Commercial history[edit]

The craft work on tanzanite.
Manuel de Souza, a tailor and part-time gold prospector living in Arusha (Tanzania), found transparent fragments of vivid blue and blue-purple gem crystals on a ridge near Mererani, some 40 km southeast of Arusha. He assumed that the mineral was olivine (peridot) but after soon realizing it wasn't, he concluded it was "dumortierite", a blue non-gem mineral. Shortly thereafter, the stones were shown to John Saul, aNairobi-based consulting geologist and gemstone wholesaler who was then mining aquamarine in the region around Mount Kenya. Saul, with a Ph.D. from M.I.T., who later discovered the famous ruby deposits in the Tsavo area of Kenya, eliminated dumortierite and cordierite as possibilities, and sent samples to his father, Hyman Saul, vice president at Saks Fifth Avenue in New York. Hyman Saul brought the samples across the street to the Gemological Institute of America who correctly identified the new gem as a variety of the mineral zoisite. Correct identification was also made by mineralogists at Harvard University, theBritish Museum, and Heidelberg University, but the very first person to get the identification right was Ian McCloud, a Tanzanian government geologist based in Dodoma.[8][9]
Scientifically called "blue zoisite", the gemstone was renamed as tanzanite by Tiffany & Co., who wanted to capitalize on the rarity and single location of the gem, and thought that "blue zoisite" (which might be pronounced like "blue suicide") wouldn't sell well.[10] Tiffany's original campaign advertised that tanzanite could now be found in two places: "in Tanzania and at Tiffany's".
From 1967, an estimated two million carats of tanzanite were mined in Tanzania before the mines were nationalized by the Tanzanian government in 1971.
Multicoloured Tanzanite Crystal
Untreated Tanzanite Gemstone
Hologram of a Trichroic Tanzanite Specimen
A rough sample of tanzanite.

Recent Tanzanite Mining Developments[edit]

In 1990, the Tanzanian government split the Tanzanite mines into four sections: Blocks A, B, C and D. Blocks A and C were awarded to large operators, while Blocks B and D were reserved for the local miners. In 2005 the government renewed the lease of Block C mine toTanzanite One, who paid 40 million dollars for their lease and mining license.[citation needed]
In June 2003, the Tanzanian government introduced legislation banning the export of unprocessed tanzanite to India (like many gemstones, most tanzanite is cut in Jaipur). The ban has been rationalized as an attempt to spur development of local processing facilities, thereby boosting the economy and recouping profits. This ban was phased in over a two-year period, until which time only stones over 0.5 grams were affected.[citation needed] In 2010, the government of Tanzania banned the export of rough stones weighing more than one gram.[11]
TanzaniteOne Mining Ltd is owned by Richland Resources, but a 2010 law in Tanzania required them to cede 50% ownership of their mining license to the Tanzanian State Mining Company (Stamico). Production in 2011 amounted to 2.4 million carats, earning them $24 million.[12]
The world's largest rough tanzanite was a 16,839 carat (3.38 kg, or 7.46 lb) stone mined by TanzaniteOne in 2005.[13]

Factors affecting value: grading[edit]

There is no universally accepted method of grading colored gemstones. TanzaniteOne, a major commercial player in the tanzanite market, through its non-profit subsidiary, The Tanzanite Foundation,[14] has introduced its own color-grading system.[15] The new system's color-grading scales divide tanzanite colors into a range of hues, between bluish-violet and violetish-blue.
The normal primary and secondary hues in tanzanite are blue and violet. Untreated tanzanite is a trichroic gemstone, meaning that light that enters this anisotropic crystal gets refracted on different paths, with different color absorption on each of the three optical axes. As a result of this phenomenon, a multitude of colors have been observed in various specimens: shades of purple, violet, blue, cyan, green, yellow, brown and red. After heating, tanzanite becomes dichroic. The dichroic colors range from bluish-violet to violetish-blue.[16]
Clarity grading in colored gemstones is based on the eye-clean standard, that is, a gem is considered flawless if no inclusions are visible with the unaided eye (assuming 20/20 vision).[16] The Gemological Institute of America classifies tanzanite as a Type I gemstone, meaning it is normally eye-clean. Gems with eye-visible inclusions will be traded at deep discounts.

Heat treatment[edit]

Tanzanite forms as a brownish crystal and is trichroic - which means it shows three colors - brown, blue and violet concurrently. Heating - either occurring underground naturally by metamorphic occurrences or above ground by man in a furnace removes the brown or burgundy color component to produce a stronger purplish-blue color and makes the stone "dichroic" which means it only reflects blue and violet.[17] Rarely, gem-quality tanzanite will heat to a green primary hue, most always accompanied by a blue or violet secondary hue. These green tanzanite have some meaningful value in the collector market, but are seldom of interest to commercial buyers.[18]
When heat treated in a furnace, the temperature is usually between 370-390 degrees Celsius for 30 minutes. The stones should not have any cracks or bubbles, as they could shatter or the cracks/ bubble could increase in size during furnace heating.[19]
Some stones found close to the surface in the early days of the discovery (in an area now called D block) were gem-quality blue without the need for heat treatment - probably the result of a wild fire in the area which heated the stones underground. This gave rise to the idea that "D block" stone were more desirable than tanzanite found in other areas of the small tanzanite mining area.
Since heat treatment is universal, it has no effect on price, and finished gems are assumed to be heat-treated. Gemological Institute of America states that the source of heating is gemologically undetectable, but is assumed because of its prevalence.[20]
Tanzanite may be subjected to other forms of treatment as well. Recently, coated Tanzanites were discovered and tested by the AGTA and AGL laboratories.[21] A thin layer containing cobalt, determined by X-ray fluorescence, had been applied to improve the color. It was noted that "coatings in particular are not considered permanent", and in the United States are required to be disclosed at the point of sale.