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Growth II Twinning, defects, and polymorphism Jon Price
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Congratulations…it’s twins! Rational, symmetrical intergrowth of structures This raises the internal energy Growth twins - free growth accidents, where a lattice becomes offset during nucleation Transformation twins - movement of parts of the lattice when internal symmetry changes These may be contact (planar face) or penetration (throughgoing) twins. Gliding twins - offsets in the lattice as a strain (in response to a stress). Polysynthetic Chromite contact twins Staurolite penetration twins
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Common Twin Laws Triclinic Common Twin Laws Triclinic Albite twinning: plagioclase feldspars (CaAl,NaSi)AlSi 2 O 8 commonly show b-axis perpendicular polysynthetic twinning Pericline twinning: microcline, KAlSi 3 O 8, develops twining around the [010] axis when it transforms from a monoclinic structure X-polar photomicrograph by K. Hollocher, Union http://open-adit.com
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Common Twin Laws Monoclinic Common Twin Laws Monoclinic Manebach twinning: orthoclase, KAlSi 3 O 8, contact twin. Very common. Formed from accidental growth. Carlsbad twinning: orthoclase and sanidine, KAlSi 3 O 8, develop penetration twining around the [001]. Formed from accidental growth. Baveno twinning: orthoclase, KAlSi 3 O 8, develops contact twin during accidental growth. http://open-adit.com
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Common Twin Laws Monoclinic Common Twin Laws Monoclinic Swallow tail twinning: gypsum, CaSO 4 2H 2 O, develops contact twin during accidental growth. Most are cyclical contacts on {011}. Rutile (TiO 2 ) and cassiterite (SnO 2 ) are examples. Tetragonal http://open-adit.com
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Common Twin Laws Hexagonal Common Twin Laws Hexagonal Calcite twinning: Common contact twins are {0001} and rhombohedron. The right from can also can be stress Induced. Brazil twinning and daupine twinning: Penetration quartz twins resulting from transformation. http://open-adit.com
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Common Twin Laws Isometric Common Twin Laws Isometric Spinel twinning: contact twin parallel to an octahedron common to spinel (MgAl 2 O 4 ) Iron cross twin: Pyrite (FeS 2 ), 2/m class, may have pentration twinning of the forms with appearant 3A 4 symmetry. http://open-adit.com
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Defects Missing atoms (vacancies) Impurities Edge dislocations Screw dislocations Interlayered structures Twins
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Non-stoichiometric atoms Schottky defect Image from Perkins, 1998
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Frenkle defect Edge defect Image from Perkins, 1998
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Edge defect Screw dislocation AFM image of growth spiral on graphite along [001]. MIT STM image of PtNi alloy edge defects Michael Schmid, IAP/TU Wien
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Importance of defects Incorporation of non-stoichiometric elements (non substitution) Color Incorporation of foreign materials inclusions Can produce diagnostic characteristics Twinning in feldspar
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Energy Minimization Everything explained in the course thus far is the result of energy minimization! Examples? In nature, energy is the only commodity.
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Energy Minimization - a system will assume a state of minimum energy. Parameterizing energy - the Gibb’s Free Energy equation G = E + PV - TS E is a measurement of lattice energy, or the sum of bond energy P is pressure V is molar volume T is temp S is entropynote: E + PV = H
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So Free Energy is dependent on: 1. The nature of the bonding 2. Pressure 3. Temperature 4. Degree of disorder
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The Carbon System Graphite - steep dG/dP Diamond - higher initial G, shallow dG/dP
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Image modified from Zoltai and Stout, 1984 Diamond’s excited state
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Poly morph - many forms These abound in Earth Materials and can be of great use in pinning down the conditions at which the mineral formed.
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Why can we observe graphite and diamond at the same time? There is a place where both phases share the same G, but at room T, this is ~14 kbar!
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At P = 5 kbar
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Image from Pauling, 1970
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Phase Diagram Recall that as you go into the Earth, both P and T increase These two variables control phase stability of compositions in the earth. On the left is a map for phases of carbon
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Reconstruction vs. displacement Displacement requires less transition energy because lattices are just “tweaked” Reconstruction requires substantial excess energy to move things to new configuration
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Polymorphs
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From Blackburn & Dennen, 1998
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Silica Polymorphs
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More ‘morphs CaCO 3 AlSiO 5
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Order-disorder Reorganization of atoms into more ordered arrangements Decrease in T produces higher order G = E + PV - TS Change in structure accompanies change in order.
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Alkali Feldspar Order-disorder M T T
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Polytypism Polymorphs that differ only in the stacking of identical, two-dimensional sheets or layers. Cell dimensions parallel to sheets are identical Spacing between sheets is related by multiples.
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1. Increasing P results in structures with high densities and large CN are favored 2. Increasing T favors low density and CN 3. High-T modifications often has highest symmetry
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In summary - Polymorphism is a reconfiguration of chemical components in response to changing energy. Polymorphs therefore have the same composition but differing structures.
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