- •Contents
- •Foreword to the English translation
- •Preface
- •1 Introduction
- •1.1 Historical review
- •1.2 The birth of the concept of crystal growth
- •1.3 Morphology, perfection, and homogeneity
- •1.4 Complicated and complex systems
- •References
- •Suggested reading
- •2 Crystal forms
- •2.1 Morphology of crystals – the problems
- •References
- •Suggested reading
- •3 Crystal growth
- •3.1 Equilibrium thermodynamics versus kinetic thermodynamics
- •3.2 Driving force
- •3.3 Heat and mass transfer
- •3.4 Examples of mass transfer
- •3.6 Nucleation
- •3.7 Lattice defects
- •3.8 Interfaces
- •3.9 Spiral growth
- •3.10 Growth mechanism and morphology of crystals
- •3.11 Morphological instability
- •3.12 Driving force and morphology of crystals
- •3.13 Morphodroms
- •3.14 Element partitioning
- •3.15 Inclusions
- •References
- •Suggested reading
- •4 Factors determining the morphology of polyhedral crystals
- •4.1 Forms of polyhedral crystals
- •4.2 Structural form
- •4.3 Equilibrium form
- •4.4 Growth forms
- •4.4.1 Logical route for analysis
- •4.4.2 Anisotropy involved in the ambient phase
- •4.4.3 Whiskers
- •MAJOR FACTORS
- •METHODOLOGY
- •IMPURITIES
- •AMBIENT PHASES AND SOLVENT COMPONENTS
- •4.4.7 Factors controlling growth forms
- •References
- •Suggested reading
- •5 Surface microtopography of crystal faces
- •5.1 The three types of crystal faces
- •5.2 Methods of observation
- •5.3 Spiral steps
- •5.4 Circular and polygonal spirals
- •5.5 Interlaced patterns
- •5.6 Step separation
- •5.7 Formation of hollow cores
- •5.8 Composite spirals
- •5.9 Bunching
- •5.10 Etching
- •References
- •Suggested reading
- •6 Perfection and homogeneity of single crystals
- •6.1 Imperfections and inhomogeneities seen in single crystals
- •6.2 Formation of growth banding and growth sectors
- •6.3 Origin and spatial distribution of dislocations
- •References
- •7 Regular intergrowth of crystals
- •7.1 Regular intergrowth relations
- •7.2 Twinning
- •7.2.1 Types of twinning
- •7.2.2 Energetic considerations
- •7.2.4 Penetration twins and contact twins
- •7.2.5 Transformation twin
- •7.2.6 Secondary twins
- •7.3 Parallel growth and other intergrowth
- •7.4 Epitaxy
- •7.5 Exsolution, precipitation, and spinodal decomposition
- •References
- •Suggested reading
- •8 Forms and textures of polycrystalline aggregates
- •8.1 Geometrical selection
- •8.2 Formation of banding
- •8.3 Spherulites
- •8.4 Framboidal polycrystalline aggregation
- •References
- •Suggested reading
- •9 Diamond
- •9.1 Structure, properties, and use
- •9.2 Growth versus dissolution
- •9.3 Single crystals and polycrystals
- •9.4 Morphology of single crystals
- •9.4.1 Structural form
- •9.4.2 Characteristics of {111}, {110}, and {100} faces
- •9.4.3 Textures seen inside a single crystal
- •9.4.4 Different solvents (synthetic diamond)
- •9.4.5 Twins
- •9.4.6 Coated diamond and cuboid form
- •9.4.7 Origin of seed crystals
- •9.4.8 Type II crystals showing irregular forms
- •References
- •Suggested reading
- •10 Rock-crystal (quartz)
- •10.1 Silica minerals
- •10.2 Structural form
- •10.3 Growth forms
- •10.4 Striated faces
- •10.5 Growth forms of single crystals
- •10.5.1 Seed crystals and forms
- •10.5.2 Effect of impurities
- •10.5.3 Tapered crystals
- •10.6 Twins
- •10.6.1 Types of twins
- •10.6.2 Japanese twins
- •10.6.3 Brazil twins
- •10.7 Scepter quartz
- •10.8 Thin platy crystals and curved crystals
- •10.9 Agate
- •References
- •11 Pyrite and calcite
- •11.1 Pyrite
- •11.1.2 Characteristics of surface microtopographs
- •11.1.4 Polycrystalline aggregates
- •11.2 Calcite
- •11.2.1 Habitus
- •11.2.2 Surface microtopography
- •References
- •12 Minerals formed by vapor growth
- •12.1 Crystal growth in pegmatite
- •12.3 Hematite and phlogopite in druses of volcanic rocks
- •References
- •13 Crystals formed by metasomatism and metamorphism
- •13.1 Kaolin group minerals formed by hydrothermal replacement (metasomatism)
- •13.2 Trapiche emerald and trapiche ruby
- •13.3 Muscovite formed by regional metamorphism
- •References
- •14 Crystals formed through biological activity
- •14.1 Crystal growth in living bodies
- •14.2 Inorganic crystals formed as indispensable components in biological activity
- •14.2.1 Hydroxyapatite
- •14.2.2 Polymorphic minerals of CaCO3
- •14.2.3 Magnetite
- •14.3 Crystals formed through excretion processes
- •14.4 Crystals acting as possible reservoirs for necessary components
- •14.5 Crystals whose functions are still unknown
- •References
- •Appendixes
- •A.1 Setting of crystallographic axes
- •A.2 The fourteen Bravais lattices and seven crystal systems
- •A.3 Indexing of crystal faces and zones
- •A.4 Symmetry elements and their symbols
- •Materials index
- •Subject index
194 Diamond
Table 9.4 Morphology of diamond
Sunagawa’s classification
Single crystalline |
octahedral, tetrahedral, dodecahedral with curved faces, twins |
Polycrystalline |
ballas, bort, short bort, hailstone bort, framesite, stuwartite, carbonado |
Two-stage growth |
(a) coated stone, cuboid |
(b)octahedral growth on cuboid seed
9.4.8Type II crystals showing irregular forms
Natural diamonds grew in the mantle deep under the Earth and were
brought up to the surface by the rapidly ascending movement of kimberlite or lamproite magma. During this process, crystals were partially dissolved and also experienced plastic deformation due to stress associated with the rapid ascending movement. The evidence supporting this is recorded in the form of tangled dislocations observed in single crystals, the occurrence of slip lines, and bent crystals.
Type I diamond has a high content of nitrogen, which occurs in the form of precipitated nitrogen platelets or aggregates. In contrast to the fact that Type I crystals may be regarded as a C–N alloy, Type II diamond contains nitrogen at less than part per million order, and can be regarded as a purer carbon crystal. As can be seen from the large differences in critical shear stress that causes plastic deformation between pure aluminum and duralumin, an Al alloy containing less than 2% Cu, Type II (corresponding to pure metal) is plastically weaker than Type I (corresponding to an alloy), and thus it is expected that Type II diamond will be plastically more deformed and will eventually fracture before Type I crystals under the same applied shear stress.
External forms of diamond crystals are used as a criterion in sorting rough stones of diamond. Rounded crystals, octahedrons, and cuboids are all grouped as Type I crystals, and are further subdivided by color and forms on a fashioning basis. In contrast, crystals showing irregular or platy forms without distinct crystal faces are all classified as Type II. This empirical classification has been found to be essentially correct on checking using the transmittance of ultra-violet rays. Namely, Type I crystals exhibit rounded, polyhedral forms, and Type II crystals are characterized by irregular and platy forms, not bounded by crystallographic faces. The following reasons have been suggested as explanations [19].
(1)Irregular forms of Type II crystals may represent broken forms of what were originally polyhedral forms in the Earth and became irregular either (i) by the uplifting process or (ii) due to shock received during or after mining operations.
(2)The remarkable anisotropy in the dissolution in the magma may have contributed to the irregularity.
9.4 Morphology of single crystals 195
Figure 9.20. Type II diamond showing irregular forms.
(3)The growth of diamond in interstices of solid particles may be an explanation.
(4)Polyhedral (principally octahedral) crystals of Type I may have appeared due to selective adsorption of impurities to suppress the growth rate of {111}, and therefore pure Type II grew without such an effect, thus resulting in irregular forms.
The last explanation, i.e. the development of {111} due to impurity adsorption, can be easily refuted on the basis of the anisotropy involved in diamond structure (PBC analysis). The likelihood of (2) and (3) being true is also remote.
As seen from Fig. 9.20, Type II crystals show irregular forms and their surfaces show minute undulation, indicating that the surface was etched after the irregular forms appeared. Under a polarization microscope, Type II crystals show a characteristic tatami-mat pattern [20] formed by crossing slip lines parallel to {111} or they universally show strain birefringence. X-ray topographs of Type II crystals consist of irregular areas showing contrast images, and those are entirely out of contrast, which indicates that the crystal is bent. The X-ray topographic characteristics are very different from those seen in Type I crystals. All this indicates that Type II crystals are plastically more heavily deformed than Type I crystals. It is anticipated that the probability of Type II crystals taking irregular forms is much higher than for Type I crystals, if deformation proceeds further and crystals are broken. Judging from the observation that Type II crystals show surface etching, we may conclude that the morphological characteristics of irregular or platy forms