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Mineral assembly
โ€ข Most minerals will deal with ionic bonds
between cations and anions (or anionic
subunits which are themselves mostly
covalent but do not dissociate)
โ€ข Assembly of minerals can be viewed as
the assembly of individual ions/subunits
into a repeatable framework
โ€ข This repeatable framework is a crystal or
crystalline material
Mineral Assembly
โ€ข Isotropic โ€“ same properties in every
direction
โ€ข Anisotropic- different properties in different
directions ๏ƒ  most minerals are this type
โ€ข Assembly of ions from melts, water, or
replacement reactions which form bonds
โ€ข The matrices the ions are in always contain
many different ions โ€“ different conditions of
formation for the same mineral creates
differencesโ€ฆ
Polymorphs
โ€ข Two minerals with the same chemical formula but
different chemical structures
โ€ข What can cause these transitions??
โ€ขsphalerite-wurtzite
โ€ขpyrite-marcasite
โ€ขcalcite-aragonite
โ€ขQuartz forms (10)
โ€ขdiamond-graphite
Complexes ๏ƒ  Minerals
โ€ข Metals in solution are coordinated with ligands
(Such as H2O, Cl-, etc.)
โ€ข Formation of a sulfide mineral requires direct
bonding between metals and sulfide
โ€“ requires displacement of these ligands and
deprotonation of the sulfide
โ€ข Cluster development is the result of these
requirements
Mineral growth
โ€ข Ions come together in a crystal โ€“ charge is
balanced across the whole
โ€ข How do we get large crystals??
โ€“ Different mechanisms for the growth of
particular minerals
โ€“ All a balance of kinetics (how fast) and
thermodynamics (most stable)
Nucleation
โ€ข Aggregation of molecules builds larger and
larger molecules โ€“ becomes a nucleus at
some point
โ€ข Nucleus โ€“ size of this is either big enough
to continue growth or will re-dissolve
(Critical Size)
โ€ข Overall rate of nucleus formation vs.
crystal growth determines crystal
size/distribution
Crystal Shapes
โ€ข Shape is determined by atomic
arrangements
โ€ข Some directions grow faster than others
โ€ข Morphology can be distinct for the
conditions and speed of mineral
nucleation/growth (and growth along specific
axes)
Ostwald Ripening
Larger crystals are more stable than smaller crystals
โ€“ the energy of a system will naturally trend towards
the formation of larger crystals at the expense of
smaller ones
In a sense, the smaller crystals are โ€˜feedingโ€™ the
larger ones through a series of dissolution and
precipitation reactions
Figure 3-17. โ€œOstwald ripeningโ€ in a monomineralic material. Grain boundaries with significant
negative curvature (concave inward) migrate toward their center of curvature, thus eliminating
smaller grains and establishing a uniformly coarse-grained equilibrium texture with 120o grain
intersections (polygonal mosaic). ยฉ John Winter and Prentice Hall
Small crystalsโ€ฆ
โ€ข In the absence of ripening, get a lot of very
small crystals forming and no larger
crystals.
โ€ข This results in a more massive
arrangement
โ€ข Microcrystalline examples (Chert)
โ€ข Massive deposits (common in ore
deposits)
Topotactic Alignment
โ€ขAlignment of smaller grains in space โ€“ due to magnetic
attraction, alignment due to biological activity (some microbes
make a compass with certain minerals), or chemical/
structural alignment โ€“ aka oriented attachment
Igneous Textures
Figure 3-1. Idealized rates of
crystal nucleation and growth as
a function of temperature below
the melting point. Slow cooling
results in only minor
undercooling (Ta), so that rapid
growth and slow nucleation
produce fewer coarse-grained
crystals. Rapid cooling permits
more undercooling (Tb), so that
slower growth and rapid
nucleation produce many fine-
grained crystals. Very rapid
cooling involves little if any
nucleation or growth (Tc)
producing a glass.

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Lecture 5 - Crystallization.ppt

  • 1. Mineral assembly โ€ข Most minerals will deal with ionic bonds between cations and anions (or anionic subunits which are themselves mostly covalent but do not dissociate) โ€ข Assembly of minerals can be viewed as the assembly of individual ions/subunits into a repeatable framework โ€ข This repeatable framework is a crystal or crystalline material
  • 2. Mineral Assembly โ€ข Isotropic โ€“ same properties in every direction โ€ข Anisotropic- different properties in different directions ๏ƒ  most minerals are this type โ€ข Assembly of ions from melts, water, or replacement reactions which form bonds โ€ข The matrices the ions are in always contain many different ions โ€“ different conditions of formation for the same mineral creates differencesโ€ฆ
  • 3. Polymorphs โ€ข Two minerals with the same chemical formula but different chemical structures โ€ข What can cause these transitions?? โ€ขsphalerite-wurtzite โ€ขpyrite-marcasite โ€ขcalcite-aragonite โ€ขQuartz forms (10) โ€ขdiamond-graphite
  • 4. Complexes ๏ƒ  Minerals โ€ข Metals in solution are coordinated with ligands (Such as H2O, Cl-, etc.) โ€ข Formation of a sulfide mineral requires direct bonding between metals and sulfide โ€“ requires displacement of these ligands and deprotonation of the sulfide โ€ข Cluster development is the result of these requirements
  • 5.
  • 6.
  • 7.
  • 8. Mineral growth โ€ข Ions come together in a crystal โ€“ charge is balanced across the whole โ€ข How do we get large crystals?? โ€“ Different mechanisms for the growth of particular minerals โ€“ All a balance of kinetics (how fast) and thermodynamics (most stable)
  • 9. Nucleation โ€ข Aggregation of molecules builds larger and larger molecules โ€“ becomes a nucleus at some point โ€ข Nucleus โ€“ size of this is either big enough to continue growth or will re-dissolve (Critical Size) โ€ข Overall rate of nucleus formation vs. crystal growth determines crystal size/distribution
  • 10. Crystal Shapes โ€ข Shape is determined by atomic arrangements โ€ข Some directions grow faster than others โ€ข Morphology can be distinct for the conditions and speed of mineral nucleation/growth (and growth along specific axes)
  • 11. Ostwald Ripening Larger crystals are more stable than smaller crystals โ€“ the energy of a system will naturally trend towards the formation of larger crystals at the expense of smaller ones In a sense, the smaller crystals are โ€˜feedingโ€™ the larger ones through a series of dissolution and precipitation reactions
  • 12. Figure 3-17. โ€œOstwald ripeningโ€ in a monomineralic material. Grain boundaries with significant negative curvature (concave inward) migrate toward their center of curvature, thus eliminating smaller grains and establishing a uniformly coarse-grained equilibrium texture with 120o grain intersections (polygonal mosaic). ยฉ John Winter and Prentice Hall
  • 13. Small crystalsโ€ฆ โ€ข In the absence of ripening, get a lot of very small crystals forming and no larger crystals. โ€ข This results in a more massive arrangement โ€ข Microcrystalline examples (Chert) โ€ข Massive deposits (common in ore deposits)
  • 14. Topotactic Alignment โ€ขAlignment of smaller grains in space โ€“ due to magnetic attraction, alignment due to biological activity (some microbes make a compass with certain minerals), or chemical/ structural alignment โ€“ aka oriented attachment
  • 15. Igneous Textures Figure 3-1. Idealized rates of crystal nucleation and growth as a function of temperature below the melting point. Slow cooling results in only minor undercooling (Ta), so that rapid growth and slow nucleation produce fewer coarse-grained crystals. Rapid cooling permits more undercooling (Tb), so that slower growth and rapid nucleation produce many fine- grained crystals. Very rapid cooling involves little if any nucleation or growth (Tc) producing a glass.