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Mineral assembly
• Most minerals will deal with ionic bonds
between cations and anions (or anionic
subunits which are themselves mostly
covalent but do not dissociate)
• Assembly of minerals can be viewed as
the assembly of individual ions/subunits
into a repeatable framework
• This repeatable framework is a crystal or
crystalline material
Mineral Assembly
• Isotropic – same properties in every
direction
• Anisotropic- different properties in different
directions  most minerals are this type
• Assembly of ions from melts, water, or
replacement reactions which form bonds
• The matrices the ions are in always contain
many different ions – different conditions of
formation for the same mineral creates
differences…
Polymorphs
• Two minerals with the same chemical formula but
different chemical structures
• What can cause these transitions??
•sphalerite-wurtzite
•pyrite-marcasite
•calcite-aragonite
•Quartz forms (10)
•diamond-graphite
Complexes  Minerals
• Metals in solution are coordinated with ligands
(Such as H2O, Cl-, etc.)
• Formation of a sulfide mineral requires direct
bonding between metals and sulfide
– requires displacement of these ligands and
deprotonation of the sulfide
• Cluster development is the result of these
requirements
Mineral growth
• Ions come together in a crystal – charge is
balanced across the whole
• How do we get large crystals??
– Different mechanisms for the growth of
particular minerals
– All a balance of kinetics (how fast) and
thermodynamics (most stable)
Nucleation
• Aggregation of molecules builds larger and
larger molecules – becomes a nucleus at
some point
• Nucleus – size of this is either big enough
to continue growth or will re-dissolve
(Critical Size)
• Overall rate of nucleus formation vs.
crystal growth determines crystal
size/distribution
Crystal Shapes
• Shape is determined by atomic
arrangements
• Some directions grow faster than others
• 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
– 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 ‘feeding’ the
larger ones through a series of dissolution and
precipitation reactions
Figure 3-17. “Ostwald ripening” 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). © John Winter and Prentice Hall
Small crystals…
• In the absence of ripening, get a lot of very
small crystals forming and no larger
crystals.
• This results in a more massive
arrangement
• Microcrystalline examples (Chert)
• Massive deposits (common in ore
deposits)
Topotactic Alignment
•Alignment of smaller grains in space – due to magnetic
attraction, alignment due to biological activity (some microbes
make a compass with certain minerals), or chemical/
structural alignment – 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 • Most minerals will deal with ionic bonds between cations and anions (or anionic subunits which are themselves mostly covalent but do not dissociate) • Assembly of minerals can be viewed as the assembly of individual ions/subunits into a repeatable framework • This repeatable framework is a crystal or crystalline material
  • 2. Mineral Assembly • Isotropic – same properties in every direction • Anisotropic- different properties in different directions  most minerals are this type • Assembly of ions from melts, water, or replacement reactions which form bonds • The matrices the ions are in always contain many different ions – different conditions of formation for the same mineral creates differences…
  • 3. Polymorphs • Two minerals with the same chemical formula but different chemical structures • What can cause these transitions?? •sphalerite-wurtzite •pyrite-marcasite •calcite-aragonite •Quartz forms (10) •diamond-graphite
  • 4. Complexes  Minerals • Metals in solution are coordinated with ligands (Such as H2O, Cl-, etc.) • Formation of a sulfide mineral requires direct bonding between metals and sulfide – requires displacement of these ligands and deprotonation of the sulfide • Cluster development is the result of these requirements
  • 5.
  • 6.
  • 7.
  • 8. Mineral growth • Ions come together in a crystal – charge is balanced across the whole • How do we get large crystals?? – Different mechanisms for the growth of particular minerals – All a balance of kinetics (how fast) and thermodynamics (most stable)
  • 9. Nucleation • Aggregation of molecules builds larger and larger molecules – becomes a nucleus at some point • Nucleus – size of this is either big enough to continue growth or will re-dissolve (Critical Size) • Overall rate of nucleus formation vs. crystal growth determines crystal size/distribution
  • 10. Crystal Shapes • Shape is determined by atomic arrangements • Some directions grow faster than others • 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 – 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 ‘feeding’ the larger ones through a series of dissolution and precipitation reactions
  • 12. Figure 3-17. “Ostwald ripening” 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). © John Winter and Prentice Hall
  • 13. Small crystals… • In the absence of ripening, get a lot of very small crystals forming and no larger crystals. • This results in a more massive arrangement • Microcrystalline examples (Chert) • Massive deposits (common in ore deposits)
  • 14. Topotactic Alignment •Alignment of smaller grains in space – due to magnetic attraction, alignment due to biological activity (some microbes make a compass with certain minerals), or chemical/ structural alignment – 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.