The document discusses theoretical density calculations for crystalline materials. It defines theoretical density as the mass of a material divided by its volume. The mass is calculated as the number of atoms in the unit cell multiplied by the atomic weight. The volume is the volume of the unit cell. It provides an example calculation for the theoretical density of copper using its atomic radius, face-centered cubic crystal structure, atomic weight, and number of atoms in the unit cell. It then compares the calculated theoretical density to copper's measured density.
The document discusses theoretical density calculations for crystalline materials. It defines theoretical density as the mass of a material divided by its volume. The mass is calculated as the number of atoms in the unit cell multiplied by the atomic weight. The volume is the volume of the unit cell. It provides an example calculation for the theoretical density of copper using its atomic radius, face-centered cubic crystal structure, atomic weight, and number of atoms in the unit cell. It then compares the calculated theoretical density to copper's measured density.
The document discusses theoretical density calculations for crystalline materials. It defines theoretical density as the mass of a material divided by its volume. The mass is calculated as the number of atoms in the unit cell multiplied by the atomic weight. The volume is the volume of the unit cell. It provides an example calculation for the theoretical density of copper using its atomic radius, face-centered cubic crystal structure, atomic weight, and number of atoms in the unit cell. It then compares the calculated theoretical density to copper's measured density.
The document discusses theoretical density calculations for crystalline materials. It defines theoretical density as the mass of a material divided by its volume. The mass is calculated as the number of atoms in the unit cell multiplied by the atomic weight. The volume is the volume of the unit cell. It provides an example calculation for the theoretical density of copper using its atomic radius, face-centered cubic crystal structure, atomic weight, and number of atoms in the unit cell. It then compares the calculated theoretical density to copper's measured density.
mass = (number of atoms per unit cell) x (mass of each atom)
mass of each atom = atomic weight/Avogadro’s number
n = number of atoms associated with each unit cell
A = atomic weight (g/mol) VC = volume of the unit cell (cm3 per unit cell) NA = Avogadro’s number (6.022 x 1023 atoms/mol)
School of Mechanical and Building Sciences, VIT University, Vellore
Theoretical Density Computation for Copper Question: Copper has an atomic radius of 0.128 nm, an FCC crystal structure, and an atomic weight of 63.5 g/mol. Compute its theoretical density and compare the answer with its measured density.
Solution : the crystal structure is FCC, n, the number of atoms per unit cell, is 4. Furthermore, the atomic weight ACu is given as 63.5 g/mol. • The unit cell volume VC for FCC is 16R3√2, where R, the atomic radius, is 0.128 nm.
School of Mechanical and Building Sciences, VIT University, Vellore
Polymorphism and Allotropy
• Polymorphism – Same compound occurring in more than one crystal structure
– depends on both the temperature and the external pressure
– Eg. calcite, aragonite and vaterite minerals , different forms of CaCO3
– TiO2: Rutile, Anatase and Brookite
• Allotropy – Polymorphism in elemental solids
– Eg: Allotrops of carbon are diamond and graphite
– Allotrops of sulphur: Rhombic sulphur and cyclic sulphur (S8)
– Phosperous: White P, Red P, Violet P
– Iron: α-Fe, γ-Fe and δ-Fe
School of Mechanical and Building Sciences, VIT University, Vellore Crystallographic Points, Directions, and Planes • When dealing with crystalline materials, it often becomes necessary to specify a particular point within a unit cell, a crystallographic direction, or some crystallographic plane of atoms.
• Labeling conventions have been established in which three
numbers or indices are used to designate point locations, directions, and planes.
• The basis for determining index values is the unit cell, with a right-handed coordinate system consisting of three (x, y, and z) axes situated at one of the corners and coinciding with the unit cell edges, as shown in Figure.
• For some crystal systems—namely, hexagonal, rhombohedral,
monoclinic, and triclinic-
-the three axes are not mutually perpendicular.
School of Mechanical and Building Sciences, VIT University, Vellore
Point Coordinates • The position of any point located within a unit cell may be specified in terms of its coordinates as fractional multiples of the unit cell edge lengths (i.e., in terms of a, b, and c
• The position of any point located within a unit cell may be specified in terms of its coordinates as fractional multiples of the unit cell edge lengths (i.e., in terms of a, b, and c). • To illustrate, consider the unit cell and the point P situated therein as shown in Figure.
• We specify the position of P in terms of the generalized
coordinates q, r, and s where q is some fractional length of a along the x axis, r is some fractional length of b along the y axis, and s is some fractional length of c along the z axis.
• Thus, the position of P is designated using coordinates q r s with values that are less than or equal to unity. Furthermore, we have chosen not to separate these coordinates by commas or any other punctuation marks (which is the normal convention).
School of Mechanical and Building Sciences, VIT University, Vellore
Point Coordinates
School of Mechanical and Building Sciences, VIT University, Vellore
Point Coordinates Specification of Point Coordinates • Specify point coordinates for all atom positions for a BCC unit cell
School of Mechanical and Building Sciences, VIT University, Vellore
Crystallographic Directions • A crystallographic direction is defined as a line between two points, or a vector.
Steps used to determine the three directional indices:
1. A vector of convenient length is positioned such that it passes through the origin of the coordinate system. Any vector may be translated throughout the crystal lattice without alteration, if parallelism is maintained.
2. The length of the vector projection on each of the three axes is determined; these are measured in terms of the unit cell dimensions a, b, and c. 3. These three numbers are multiplied or divided by a common factor to reduce them to the smallest integer values.
4. The three indices, not separated by commas, are enclosed in
square brackets, thus: [uvw]. The u, v, and w integers correspond to the reduced projections along the x, y, and z axes, respectively. For each of the three axes, there will exist both positive and negative coordinates. Thus The [100], [110], and [111] negative indices_are also possible, which are represented by a bar over the appropriate directions within a unit cell. index. Eg. the [111 ]
School of Mechanical and Building Sciences, VIT University, Vellore
Crystallographic Directions
School of Mechanical and Building Sciences, VIT University, Vellore
Crystallographic Directions
School of Mechanical and Building Sciences, VIT University, Vellore
Crystallographic Directions - Family • For some crystal structures, several nonparallel directions with different indices are crystallographically equivalent; this means that the spacing of atoms along each direction is the same.
• The directions in a crystal are given by specifying the coordinates (u, v, w) of a point on a vector passing through the origin. It is indicated as [uvw]. For example, the direction [110] lies on a vector whose projection lengths on x and y axes are one unit.
• Directions of a form or family like [110], [101], [011] are written as <110>
<100> and <110> family <111> family
School of Mechanical and Building Sciences, VIT University, Vellore
Hexagonal Crystals • Problem – In crystals having hexagonal symmetry, some crystallographic equivalent directions will not have the same set of indices.
• This is circumvented by utilizing a four-axis, or Miller–Bravais, coordinate system as
shown in Figure.
• The three a1, a2, and a3 axes are all contained within a single plane (called the basal plane) and are at 120° angles to one another.
• The z axis is perpendicular to this basal plane.
• Directional indices, will be denoted by four indices, as [uvtw]; by
convention, the first three indices pertain to projections along the respective a1, a2, and a3 axes in the basal plane
Coordinate axis system for a
hexagonal unit cell (Miller–Bravais scheme).
School of Mechanical and Building Sciences, VIT University, Vellore
Hexagonal Crystals Conversion from the three-index system to the four-index system,
uvw uvtw Several different directions are indicated is accomplished by the following formulas: in the hexagonal unit cell 1 u 2u v 3 1 v 2v u 3 t u v w w _ _ Eg. the [010] direction becomes [1210].
School of Mechanical and Building Sciences, VIT University, Vellore
Conversion of Directional Indices for a Hexagonal Unit Cell Convert the [111] direction into the four-index system for hexagonal crystals
Solution u 1; v 1; w 1
Multiplication of the preceding indices by 3 reduces them to the lowest set, which yields values for u, v, t, and w of 1, 1, 2 and 3,_respectively. Hence, the [111] direction becomes [1123].
School of Mechanical and Building Sciences, VIT University, Vellore
