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This document discusses the crystalline structure of metals. It begins by introducing the concepts of space lattices, unit cells, and crystalline lattices which describe the ordered arrangement of atoms in solid crystalline materials. It then discusses different crystal systems including body centered cubic (BCC), face centered cubic (FCC), and hexagonal close packed (HCP) which are the principal crystal structures that most elemental metals form. Tables are provided listing properties of various metals that crystallize in BCC and FCC structures.
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- 1. L-01 ENGINEERINGMATERIALSCRYSTALLINE STRUCTURE OF METALS AND ALLOTROPY
- 2. Introduction Metals are frequently the materials being processed and often form both the tool and the machinery performing the processing.More than 50 of the known chemical elements are classified as metals, and about 40have commercial importance.Since atoms tend to assume relatively fixed positions, this gives rise to the formation of crystals in the solid state. The atoms oscillate about fixed locations and are in dynamic equilibrium rather than statically fixed2
- 3. Space latticeThe three dimensional network of imaginary lines connecting the atoms is called the space lattice.Unit cell: The smallest unit having the full symmetry of the crystal is called the unit cell.The specific unit cell for each metal is defined by its parameters which are the edges of the unit cell a, b, c and the angles .3
- 5. Crystalline latticeA crystal is a regular, repeating arrangement of atoms or molecules. In the crystalline arrangement, the particles pack efficiently together to minimize the total intermolecular energy.The regular repeating pattern that the atoms arrange in, is called the crystalline lattice.5
- 6. STMThe scanning tunneling microscope makes it possible to image the electron cloud associated individual atoms at the surface of a material.6
- 7. Polymorphism or AllotropyMany elements and compounds exist in more than one crystalline form under different conditions of temperature and pressure, this phenomenon is termed Polymorphism or Allotropy. Many industrially important metals such as iron, titanium, and cobalt undergo allotropic transformations at elevated temperatures at atmospheric pressure.Iron exists in both BCC and FCC crystal structures over the temperature range from room temperature to its melting point at 1539 deg C. 7
- 8. 8 iron exists from 273 to 912 deg C and has the BCC crystal structure.
- 9. Iron exists from 912 to 1394 deg C and has the FCC crystal structure.
- 10. Delta (δ) iron exists from 1394 to 1539 deg C which is the melting point of iron.
- 11. The crystal structure of iron is also BCC but with the larger lattice constant than iron.Crystal and Amorphous structure in MaterialsSolids may be categorized broadly into crystalline and amorphous solids, due to orderly structure of their atoms, molecules, or ions possess well defined shapes.Crystals or Grains: Metals are crystalline and are composed of well defined crystals or grains. The grains are small and are not clearly observable to the opaque nature of metals.In minerals, mostly translucent to transparent nature, the well defined crystalline shapes are clearly observable.9
- 12. Amorphous Solidshave poor or no long range order and do not solidify with the symmetry and regularity of crystalline solids.The space lattice and unit cells: The physical structure of solid materials of engineering importance depends mainly on the arrangements of the atoms, ions, or molecules that make up the solid and the bonding forces between them.10
- 13. 11If the atoms or ions of a solid are arranged in a pattern that repeat itself in three dimensions, they form a solid that has long range order (LRO) and is referred to as a crystalline material.
- 14. Examples of crystalline materials are metals, alloys, and some ceramic materials.
- 15. In contrast to crystalline materials, there are some materials whose atoms and ions are not arranged in a long range, periodic, and repeatable manner and possess only short range order (SRO).12This means that order exists only in the immediate neighborhood of an atom or molecule.
- 16. As an example, liquid water has short range order in its molecules in which one oxygen atom is covalently bonded to two hydrogen atoms.
- 17. But this order disappears, as each molecule is bonded to other molecules through week secondary bonds in a random manner.
- 18. Materials with only short range order are classified as amorphous (without form) or non crystalline.13 Atomic arrangements in crystalline solids can be described by referring the atoms to the point of intersection of a network of lines in three dimensions.
- 19. Such a network is called a space lattice (see fig a) and it can be described as an infinite three dimensional array of points.
- 20. Each point in the space lattice has identical surroundings.14In an ideal crystal the grouping of lattice points about any given point are identical with the grouping about any other lattice point in the crystal lattice.
- 21. Each space lattice can thus be described by specifying the atom positions in a repeating unit cell, such as the one heavily outlined in the following figure-b a group of atoms organized in a certain arrangement relative to each other and associated with lattice points constitutes the Motif or basis.15
- 22. 16The crystal structure may then be described as the collection of lattice and basis.
- 23. It is important to note that atoms do not necessarily coincide with lattice points.
- 24. The size and shape of the unit cell can be described by three lattice vectors a, b, and c, originating from one corner of the unit cell (fig-b).
- 25. The axial lengths a, b, and c and the inter axial angles, , and are the lattice constants of the unit cell.Crystal systems and Bravais LatticeBy assigning specific values for axial lengths and inter axial angles, unit cells of different types can be constructed.Crystallographers have shown thatonly seven different types of unit cells are necessary to create all space lattices. These crystal systems are listed below.17
- 26. 18Many of the seven crystal systems have variations of the basic unit cell.
- 27. A.J.Bravais showed that 14 standard unit cells could describe all possible lattice net works.
- 28. These Bravais lattices are illustrated in figure below.
- 29. There are four basic types of unit cells (1) simple,(2) BCC, (3) FCC, and (4) base centered.19Table: Classification of space lattices by crystal system
- 30. 20In the cubic system there are three types of unit cells simple cubic, BCC, and FCC. In the orthorhombic system are four types are represented.In the tetragonal system there are only two simple and body centered. The face centered tetragonal unit cell appears to be missing but can be constructed from four body centered tetragonal unit cells.The monoclinic system has simple and base centered unit cells, and the rhombohedral, hexagonal, and triclinic systems have only one simple type of unit cell.
- 31. Fig 3.221
- 32. PRINCIPAL METALLIC CRYSTAL STRUCTURESThere are two major types of the principal crystal structures: The principal crystal structures of elemental metals.The principal ionic and covalent crystal structures that occur in ceramic materials.Most elemental metals (about 90 percent) crystallize upon solidification into three densely packed crystal structures: body- centered cubic (BCC)-Fig-a, Face-centered cubic (FCC)-Fig-b, and hexagonal close-packed (HCP)-Fig-c.22
- 33. 23Fig 3.3a Fig 3.3b Fig 3.3c
- 34. 24The HCP structure is a denser modification of the simple hexagonal crystal structure shown in Fig. 3.2.
- 35. Most metals crystallize in these dense-packed structures because energy is released as the atoms come closer together and bond more tightly with each other.
- 36. Thus, the densely packed structures are in lower and more stable energy arrangements.25The extremely small size of the unit cells of crystalline metals that are shown in Fig. 3.3 should be emphasized.
- 37. The cubic side of the unit cell of body-centered cubic iron, for example, at room temperature is equal to 0.287 x 10-9 m, or 0.287 nanometer (nm).
- 38. Therefore, if unit cells of pure iron are lined up side by side, in 1 mm there will be 1 unit cell1mm x ------------------------------ = 3.48 x106 unit cell! 0.287 nm x 10-6 mm/ nm34,80,000
- 39. 26Let us now examine in detail the arrangement of the atoms in the three principal crystal structure unit cells.
- 40. Although an approximation, we shall consider atoms in these crystal structures to be hard spheres.27The radius of the aluminum atom in the aluminum metal is assumed to be half the inter-atomic distance, or 0.143 nm.
- 41. The atomic radii of selected metals are listed in tables 3.2 to 3.4.
- 42. Table 3.2 selected metals that have the BCC crystal structure at room temperature (20 C ) and their lattice constants and atomic radiiMetal Lattice constant a (nm) Atomic radius R(nm)Chromium 0.289 0.125Iron 0.287 0.124Molybdenum 0.315 0.136Potassium 0.533 0.231Sodium 0.429 0.186Tantalum 0.330 0.143Tungsten 0.316 0.137Vanadium 0.304 0.132Calculated from lattice constants by using Eq. (3.1), R = √3a/428
- 43. Table 3.3 selected metals that have the FCC crystal structure at room temperature (20 C) and their lattice constants and atomic radii. Metal Lattice constant a (nm) Atomic radius R (nm)Aluminum 0.405 0.143Copper 03615 0.128Gold 0.408 0.144Lead 0.495 0.175Nickel 0.352 0.125Platinum 0.393 0.139Silver 0.409 0.144Calculated from lattice constants by using Eq. (3.3), R = √2a/429
- 44. Table 3.4 selected metals that havethe HCP crystal structure at room temperature (20 C) and their lattice constants and atomic radii and c/a rato Lattice constant a (nm) Metal % deviation a c Atomic radius (nm) c/a ratio from idealityCadmium 0.2973 0.5618 0.149 1.890 + 15.7Zinc 0.2665 0.4947 0.133 1.856 +13.6Magnesium 0.3209 0.5209 0.160 1.623 -0.66Cobalt 0.2507 0.4069 0.125 1.623 -0.66Zirconium 0.3231 0.5148 0.160 1.593 -2.45Titanium 0.2950 0.4683 0.147 1.587 -281Beryllium 0.2286 0.3584 0.113 1.568 -3.98 30