- •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
10.6 Twins 213
Figure 10.12. Change in form and surface microtopographs observed in regrowth experiments on a Japanese twinned sample used as a seed [15]. When the Japanese twin grows freely, the form changes from a V-shape to a Y-shape.
sists of idiomorphic crystals of quartz less than 1 m. On quartz crystals of this size, {1010} faces do not appear, and the crystals take on a ditrigonal dipyramidal form bounded by r and z faces. A Japanese twin is considered to have been formed if two individuals conjugate on well developed r and z faces. The introduction of {1122} as the composition plane is simply due to the geometrical relation between the two individuals.
Figure 10.12 shows a series of sketches showing the variation in morphology and surface microtopography as growth proceeds, starting from a natural Japanese twin as seed grown in an industrial autoclave for quartz synthesis [15]. It is clearly seen that, starting from a partly broken Japanese twin with a V-shape, the form changes to a Y-shape when growth occurs in an open space. This experiment proves that the V-shape does not represent the upper half of an X-shape but that of a Y-shape, and therefore that the Japanese twin is not a penetration twin but a contact twin. It was later observed that natural Japanese twins occasionally exhibit a Y-shape when they grow in open spaces. Figure 10.12 also vividly demonstrates the sorts of changes that occur in the process of transformation from a rough to a smooth interface, and it may also be seen that two individuals are Dauphiné twinned.
10.6.3Brazil twins
The Brazil law is used to describe an intergrowth of rightand left-handed structures with the c-axis as the twin axis. Since this is a relation between different structures, strictly speaking this does not belong to the twin category, but it has always been treated as an important twinning phenomenon. In Brazil twins, two
214 Rock-crystal (quartz)
Figure 10.13. Brewster fringes frequently seen in amethyst crystals. L and R indicate
left-handed and right-handed structures, respectively.
individuals are in a reflection relation on {1120}, and occur as twin sectors in lamellar form bounded by {1010}, {1011}, and {0111}. Brazil twins occur universally in quartz crystals formed at lower temperatures, as in amethyst occurring in geode, and are only exceptionally found in quartz crystals formed at higher temperatures, such as quartz crystals occurring in pegmatites. One report [16] claims that Brazil twin lamellae are found in quartz particles constituting agate in geode exceeding 10 nm, and the widths of the lamellae range from nanometer to micrometer order. The so-called Brewster fringes often observed in amethyst (Fig. 10.13) are the boundaries of Brazil twin lamellae formed by the coagulation of numerous Brazil twin lamellae.
Considering the fact that the lamellae widths are of nanometer to micrometer order and that a Brazil twin is formed by combining right-handed and left-handed structures, we have to assume the presence of clusters with right-handed and lefthanded structures in the ambient phase, with the Brazil twin being formed by the joining together of these clusters. A Brazil twin is not formed by transformation from left-handed to right-handed structures while a crystal is growing by incorporation of ionic entities or SiO4 tetrahedra as the growth unit. This is in agreement with the observation that Brazil twins are universally observed in quartz crystals formed at lower temperature rather than at higher temperature, since the probability of cluster formation is higher at lower temperatures.
In amethyst crystals showing Brewster fringes, a pattern such as that shown in Fig. 10.14 is observed in the growth sectors of or on the surface of r faces, and not in
10.6 Twins 215
(a)
(b)
(c)
Figure 10.14. (a), (b) Reflection photomicrographs of weakly etched surface, and (c) the
structure of Brewster fringes on an r face (model by Lu and Sunagawa [17]). Zigzag (A in
(a) and (c)) and closed lamellae (B in (a) and (c)) appear alternately. L left-handed
quartz; R right-handed quartz.