Diamond Flashcards
Etymology of diamond
Greek adamao, I tame/I subdue, 1st c. BC
- also root for adamantine (lustre like a diamond)
- used to denote great hardness
Earliest use of diamond
- first mining occured in India (alluvial deposits)
- Sanskrit vajra, 4th c. BC
Significance of kimberlite
Diamond-bearing kimberlite discovered at Kimberley, South Africa in 1867 resulted in upper and middle classes having access to diamonds
Main diamond producing countries
India (alluvial deposits, prior to 20th c)
Brazil (18th c)
South Africa (1867)
Soviet Union (1950s)
Australia (1980s)
Canada (1990s)
Basic qualities of diamond
- pure carbon
- dense crystalline structure (3.51 g/cm3)
- cubic symmetry
- perfect octahedral cleavage
- Mohs value of 10
- high durability
- high refractive index (2.42)
- great dispersion
- colourless (can show colour due to structural defects, elemental substitution, and lab procedures)
- can fluoresce under UV
- hydrophobic; sticks slightly to grease
- very high thermal conductivity
- low electrical conductance
4Cs of diamonds
Colour
Cut
Clarity
Carat
Thermal conductivity of diamond
Very high due to covalent bonding of the carbon atoms
- 3x higher than gold and silver
Electrical conductivity of diamond
Low
- unusual when paired with high thermal conductance
Crystal structure of diamond
Cubic/isometric crystal system
- each of the crystallographic axes is the same length at 90 degrees to one another (unit cell building blocks are simple cubes)
- very strong covalently bonded carbon atoms & highly symmetrical 3D network
–> hard, durable, dense
Tetrahedron - each carbon atom is bonded to four other carbons in perfec triangular pyramid shape
What is diamond’s weakness?
Cleavage planes intersect to form octahedron
Facets
flat parts on a polished stone
Polymorph
A material of the same composition but with a different crystal structure
Eg.
graphite and diamond both have composition “C”
- in diamond, covalent bonds and cubic crystal system
- in graphite, 2D bonds are strong, but weak Van der Waals bonds between planes (sheets)
How diamonds are grouped
Gemologists and jewellers: 4Cs
Scientists: crystal chemistry variations
Crystal Chemistry Classification
Nitrogen substitution
- Type I –> N > 10 ppm
- Type II –> N < 10 ppm (N-free)
Dispersion of the nitrogen
- Type Ia –> N atoms occur in aggregates within the diamond (~98% of diamonds)
- Type Ib –> N is dispersed iwthin diamond structure
Clustering of the nitrogen
- Type IaA –> N atoms are paired
- Type IaB –> N atoms occur in quads (clusters of 4, often with vacancy at centre)
Boron content
- Type IIa –> B-free (2nd most common type @ <2%)
- Type IIb –> minute (<10 ppm) amounts of B (very rare)
Colouring of each type (crystal chemistry classification)
Yellow hue (absorption of blue light)
- Type Ia (appreciable N, clustered)
White (lack of impurities; no absorption of light across visible spectrum)
- Type IIa (no appreciable N or B substitutions)
Blue to grey hue (most light except blue is absorbed)
- Type IIb (minute B, no appreciable N)
Cause of colour - colourless
No impurities
Cause of colour - Blue to grey
Boron impurities
Cause of colour - yellow to orange, subdued to intense, or almost colourless
Nitrogen impurities