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Most Ia diamonds are a mixture of IaA and IaB material; these diamonds belong to the Cape series, named after the diamond-rich region formerly known as Cape Province in South Africa, whose deposits are largely Type Ia. Type Ia diamonds often show sharp absorption bands with the main band at 415.5 nm (N3) and weaker lines at 478 nm (N2), 465 nm ...
Additionally, diamond is unusually lipophilic, meaning grease and oil readily collect and spread on a diamond's surface, whereas in other minerals oil would form coherent drops. This property is exploited in the use of grease pencils , which apply a line of grease to the surface of a suspect diamond simulant .
Fluorescence in the life sciences is used generally as a non-destructive way of tracking or analysis of biological molecules by means of the fluorescent emission at a specific frequency where there is no background from the excitation light, as relatively few cellular components are naturally fluorescent (called intrinsic or autofluorescence).
Twinning causes natural lines, planes or cross-grains in a diamond. Graining can't be removed during the polishing process of a diamond as it is a natural plane within the diamond. Cross-graining also makes the polishing process extremely difficult for diamond cutters as a diamond only cuts against its natural grain lines and never with the grain.
A diamond with facets cut only a few degrees out of alignment can result in a poorly performing stone. For a round brilliant cut, there is a balance between "brilliance" and "fire". When a diamond is cut for too much "fire", it looks like a cubic zirconia, which gives off much more "fire" than real diamond. A well-executed round brilliant cut ...
Fluorescent nanodiamond is photostable, chemically inert, and has extended fluorescent lifetime, making it a great candidate for many biological applications. [23] Studies have shown that small photoluminescent diamond nanoparticles that remain free in the cytosol are excellent contenders for the transport of biomolecules.
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These techniques can be combined with microscopy, to map the intensity (confocal microscopy) or the lifetime (fluorescence-lifetime imaging microscopy) of the photoluminescence across a sample (e.g. a semiconducting wafer, or a biological sample that has been marked with fluorescent molecules). Modulated photoluminescence is a specific method ...