|
Intermetallics
An intermetallic (also called an intermetallic compound, intermetallic alloy, ordered intermetallic alloy, and a long-range-ordered alloy) is a type of metallic alloy that forms an ordered solid-state compound between two or more metallic elements. Intermetallics are generally hard and brittle, with good high-temperature mechanical properties. They can be classified as stoichiometric or nonstoichiometic intermetallic compounds. Although the term "intermetallic compounds", as it applies to solid phases, has been in use for many years, its introduction was regretted, for example by Hume-Rothery in 1955. Definitions Research definition Schulze in 1967 defined intermetallic compounds as ''solid phases containing two or more metallic elements, with optionally one or more non-metallic elements, whose crystal structure differs from that of the other constituents''. Under this definition, the following are included: #Electron (or Hume-Rothery) compounds #Size packing phases. e.g. ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chemical Compound
A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) containing atoms from more than one chemical element held together by chemical bonds. A molecule consisting of atoms of only one element is therefore not a compound. A compound can be transformed into a different substance by a chemical reaction, which may involve interactions with other substances. In this process, bonds between atoms may be broken and/or new bonds formed. There are four major types of compounds, distinguished by how the constituent atoms are bonded together. Molecular compounds are held together by covalent bonds; ionic compounds are held together by ionic bonds; intermetallic compounds are held together by metallic bonds; coordination complexes are held together by coordinate covalent bonds. Non-stoichiometric compounds form a disputed marginal case. A chemical formula specifies the number of atoms of each element in a compound molecule, using ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Hume-Rothery Rules
Hume-Rothery rules, named after William Hume-Rothery, are a set of basic rules that describe the conditions under which an element could dissolve in a metal, forming a solid solution. There are two sets of rules; one refers to substitutional solid solutions, and the other refers to interstitial solid solutions. Substitutional solid solution rules For substitutional solid solutions, the Hume-Rothery rules are as follows: # The atomic radius of the solute and solvent atoms must differ by no more than 15%: #: \% \text = \left ( \frac \right ) \times 100\% \le 15\%. # The crystal structures of solute and solvent must be similar. # Complete solubility occurs when the solvent and solute have the same valency. A metal is more likely to dissolve a metal of higher valency, than vice versa. # The solute and solvent should have similar electronegativity. If the electronegativity difference is too great, the metals tend to form intermetallic compounds instead of solid solutions. Inters ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Zintl Phase
In chemistry, a Zintl phase is a product of a reaction between a group 1 (alkali metal) or group 2 ( alkaline earth metal) and main group metal or metalloid (from groups 13, 14, 15, or 16). It is characterized by intermediate metallic/ ionic bonding. Zintl phases are a subgroup of brittle, high-melting intermetallic compounds that are diamagnetic or exhibit temperature-independent paramagnetism and are poor conductors or semiconductors.Sevov, S.C., Zintl Phases in Intermetallic Compounds, Principles and Practice: Progress, Westbrook, J.H.; *Freisher, R.L.: Eds.; John Wiley & Sons. Ltd., Chichester, England, 2002, pp. 113-13Slavi Chapter/ref> This type of solid is named after German chemist Eduard Zintl who investigated them in the 1930s. The term "Zintl Phases" was first used by Laves in 1941. In his early studies, Zintl noted that there was an atomic volume contraction upon the formation of these products and realized that this could indicate cation formation. He suggest ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Metalloid
A metalloid is a type of chemical element which has a preponderance of properties in between, or that are a mixture of, those of metals and nonmetals. There is no standard definition of a metalloid and no complete agreement on which elements are metalloids. Despite the lack of specificity, the term remains in use in the literature of chemistry. The six commonly recognised metalloids are boron, silicon, germanium, arsenic, antimony, and tellurium. Five elements are less frequently so classified: carbon, aluminium, selenium, polonium, and astatine. On a standard periodic table, all eleven elements are in a diagonal region of the p-block extending from boron at the upper left to astatine at lower right. Some periodic tables include a dividing line between metals and nonmetals, and the metalloids may be found close to this line. Typical metalloids have a metallic appearance, but they are brittle and only fair conductors of electricity. Chemically, they behave mostly as nonmetals ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Metallic Bonding
Metallic bonding is a type of chemical bonding that arises from the electrostatic attractive force between conduction electrons (in the form of an electron cloud of delocalized electrons) and positively charged metal ions. It may be described as the sharing of ''free'' electrons among a structure of positively charged ions (cations). Metallic bonding accounts for many physical properties of metals, such as strength, ductility, thermal and electrical resistivity and conductivity, opacity, and luster. Metallic bonding is not the only type of chemical bonding a metal can exhibit, even as a pure substance. For example, elemental gallium consists of covalently-bound pairs of atoms in both liquid and solid-state—these pairs form a crystal structure with metallic bonding between them. Another example of a metal–metal covalent bond is the mercurous ion (). History As chemistry developed into a science, it became clear that metals formed the majority of the periodic ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Laves Phase
Laves phases are intermetallic phases that have composition AB2 and are named for Fritz Laves who first described them. The phases are classified on the basis of geometry alone. While the problem of packing spheres of equal size has been well-studied since Gauss, Laves phases are the result of his investigations into packing spheres of two sizes. Laves phases fall into three Strukturbericht types: cubic MgCu2 (C15), hexagonal MgZn2 (C14), and hexagonal MgNi2 (C36). The latter two classes are unique forms of the hexagonal arrangement, but share the same basic structure. In general, the A atoms are ordered as in diamond, hexagonal diamond, or a related structure, and the B atoms form tetrahedra In geometry, a tetrahedron (plural: tetrahedra or tetrahedrons), also known as a triangular pyramid, is a polyhedron composed of four triangular faces, six straight edges, and four vertex corners. The tetrahedron is the simplest of all th ... around the A atoms for the AB2 str ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Frank–Kasper Phases
Topologically close pack (TCP) phases, also known as Frank-Kasper (FK) phases, are one of the largest groups of intermetallic compounds, known for their complex crystallographic structure and physical properties. Owing to their combination of periodic and aperiodic structure, some TCP phases belong to the class of quasicrystals. Applications of TCP phases as high-temperature structural and superconducting materials have been highlighted; however, they have not yet been sufficiently investigated for details of their physical properties. Also, their complex and often non-stoichiometric structure makes them good subjects for theoretical calculations. History In 1958, Frederick C. Frank and John S. Kasper, in their original work investigating many complex alloy structures, showed that non-icosahedral environments form an open-end network which they called the major skeleton, and is now identified as the declination locus. They came up with the methodology to pack asymmetric icosa ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Nowotny Phase
In inorganic chemistry, a Nowotny chimney ladder phase (NCL phase) is a particular intermetallic crystal structure found with certain binary compounds. NLC phases are generally tetragonal and are composed of two separate sublattices. The first is a tetragonal array of transition metal atoms, generally from group 4 through group 9 of the periodic table. Contained within this array of transition metal atoms is a second network of main group atoms, typically from group 13 (boron group) or group 14 (carbon group). The transition metal atoms form a chimney with helical zigzag chain. The main-group elements form a ladder spiraling inside the transition metal helix. The phase is named after one of the early investigators H. Nowotny. Examples are RuGa2, Mn4Si7, Ru2Ge3, Ir3Ga5, Ir4Ge5 V17Ge31, Cr11Ge19, Mn11Si19, Mn15Si26, Mo9Ge16, Mo13Ge23, Rh10Ga17, and Rh17Ge22. In RuGa2 the ruthenium atoms in the chimney are separated by 329 pm. The gallium atoms spiral around the Ru chimney with a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carbide
In chemistry, a carbide usually describes a compound composed of carbon and a metal. In metallurgy, carbiding or carburizing is the process for producing carbide coatings on a metal piece. Interstitial / Metallic carbides The carbides of the group 4, 5 and 6 transition metals (with the exception of chromium) are often described as interstitial compounds. These carbides have metallic properties and are refractory. Some exhibit a range of stoichiometries, being a non-stoichiometric mixture of various carbides arising due to crystal defects. Some of them, including titanium carbide and tungsten carbide, are important industrially and are used to coat metals in cutting tools. The long-held view is that the carbon atoms fit into octahedral interstices in a close-packed metal lattice when the metal atom radius is greater than approximately 135 pm: *When the metal atoms are cubic close-packed, (ccp), then filling all of the octahedral interstices with carbon achieves 1:1 s ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Solid Solution
A solid solution, a term popularly used for metals, is a homogenous mixture of two different kinds of atoms in solid state and have a single crystal structure. Many examples can be found in metallurgy, geology, and solid-state chemistry. The word "solution" is used to describe the intimate mixing of components at the atomic level and distinguishes these homogeneous materials from physical mixtures of components. Two terms are mainly associated with solid solutions - ''solvents'' and ''solutes,'' depending on the relative abundance of the atomic species. In general if two compounds are isostructural then a solid solution will exist between the end members (also known as parents). For example sodium chloride and potassium chloride have the same cubic crystal structure so it is possible to make a pure compound with any ratio of sodium to potassium (Na1-xKx)Cl by dissolving that ratio of NaCl and KCl in water and then evaporating the solution. A member of this family is sold under t ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Interstitial Compound
In materials science, an interstitial defect is a type of point crystallographic defect where an atom of the same or of a different type, occupies an interstitial site in the crystal structure. When the atom is of the same type as those already present they are known as a self-interstitial defect. Alternatively, small atoms in some crystals may occupy interstitial sites, such as hydrogen in palladium. Interstitials can be produced by bombarding a crystal with elementary particles having energy above the displacement threshold for that crystal, but they may also exist in small concentrations in thermodynamic equilibrium. The presence of interstitial defects can modify the physical and chemical properties of a material. History The idea of interstitial compounds was started in the late 1930s and they are often called Hagg phases after Hägg. Transition metals generally crystallise in either the hexagonal close packed or face centered cubic structures, both of which can be consider ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
