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Hafnium Compounds
Hafnium compounds are compounds containing the element hafnium (Hf). Due to the lanthanide contraction, the ionic radius of hafnium(IV) (0.78 ångström) is almost the same as that of zirconium(IV) (0.79 angstroms). Consequently, compounds of hafnium(IV) and zirconium(IV) have very similar chemical and physical properties. Hafnium and zirconium tend to occur together in nature and the similarity of their ionic radii makes their chemical separation rather difficult. Hafnium tends to form inorganic compounds in the oxidation state of +4. Halogens react with it to form hafnium tetrahalides. At higher temperatures, hafnium reacts with oxygen, nitrogen, carbon, boron, sulfur, and silicon. Some compounds of hafnium in lower oxidation states are known. Halides Hafnium(IV) fluoride (HfF4) is a white crystalline powder. It has a monoclinic crystal structure, with space group C2/c (No.15), and lattice constants ''a'' = 1.17 nm, ''b'' = 0.986 nm and ''c'' = 0.764 nm. Hafnium(IV) c ...
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Hafnium
Hafnium is a chemical element with the symbol Hf and atomic number 72. A lustrous, silvery gray, tetravalent transition metal, hafnium chemically resembles zirconium and is found in many zirconium minerals. Its existence was predicted by Dmitri Mendeleev in 1869, though it was not identified until 1923, by Dirk Coster and George de Hevesy, making it the penultimate stable element to be discovered (the last being rhenium in 1925). Hafnium is named after , the Latin name for Copenhagen, where it was discovered. Hafnium is used in filaments and electrodes. Some semiconductor fabrication processes use its oxide for integrated circuits at 45 nanometers and smaller feature lengths. Some superalloys used for special applications contain hafnium in combination with niobium, titanium, or tungsten. Hafnium's large neutron capture cross section makes it a good material for neutron absorption in control rods in nuclear power plants, but at the same time requires that it be removed from th ...
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Hafnium(IV) Chloride
Hafnium(IV) chloride is the inorganic compound with the formula HfCl4. This colourless solid is the precursor to most hafnium organometallic compounds. It has a variety of highly specialized applications, mainly in materials science and as a catalyst. Preparation HfCl4 can be produced by several related procedures: *The reaction of carbon tetrachloride and hafnium oxide at above 450 °C; :HfO2 + 2 CCl4 → HfCl4 + 2 COCl2 *Chlorination of a mixture of HfO2 and carbon above 600 °C using chlorine gas or sulfur monochloride: :HfO2 + 2 Cl2 + C → HfCl4 + CO2 *Chlorination of hafnium carbide above 250 °C. Separation of Zr and Hf Hafnium and zirconium occur together in minerals such as zircon, cyrtolite and baddeleyite. Zircon contains 0.05% to 2.0% hafnium dioxide HfO2, cyrtolite with 5.5% to 17% HfO2 and baddeleyite contains 1.0 to 1.8 percent HfO2.Newnham, Ivan Edgar "Purification of Hafnium Tetrachloride". November 22, 1960. Hafnium and zircon ...
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Walter De Gruyter
Walter de Gruyter GmbH, known as De Gruyter (), is a German scholarly publishing house specializing in academic literature. History The roots of the company go back to 1749 when Frederick the Great granted the Königliche Realschule in Berlin the royal privilege to open a bookstore and "to publish good and useful books". In 1800, the store was taken over by Georg Reimer (1776–1842), operating as the ''Reimer'sche Buchhandlung'' from 1817, while the school’s press eventually became the ''Georg Reimer Verlag''. From 1816, Reimer used the representative Sacken'sche Palace on Berlin's Wilhelmstraße for his family and the publishing house, whereby the wings contained his print shop and press. The building became a meeting point for Berlin salon life and later served as the official residence of the president of Germany. Born in Ruhrort in 1862, Walter de Gruyter took a position with Reimer Verlag in 1894. By 1897, at the age of 35, he had become sole proprietor of the h ...
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Crystal Bar Process
A crystal or crystalline solid is a solid material whose constituents (such as atoms, molecules, or ions) are arranged in a highly ordered microscopic structure, forming a crystal lattice that extends in all directions. In addition, macroscopic single crystals are usually identifiable by their geometrical shape, consisting of flat faces with specific, characteristic orientations. The scientific study of crystals and crystal formation is known as crystallography. The process of crystal formation via mechanisms of crystal growth is called crystallization or solidification. The word ''crystal'' derives from the Ancient Greek word (), meaning both "ice" and "rock crystal", from (), "icy cold, frost". Examples of large crystals include snowflakes, diamonds, and table salt. Most inorganic solids are not crystals but polycrystals, i.e. many microscopic crystals fused together into a single solid. Polycrystals include most metals, rocks, ceramics, and ice. A third category of sol ...
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Iodine
Iodine is a chemical element with the symbol I and atomic number 53. The heaviest of the stable halogens, it exists as a semi-lustrous, non-metallic solid at standard conditions that melts to form a deep violet liquid at , and boils to a violet gas at . The element was discovered by the French chemist Bernard Courtois in 1811 and was named two years later by Joseph Louis Gay-Lussac, after the Ancient Greek 'violet-coloured'. Iodine occurs in many oxidation states, including iodide (I−), iodate (), and the various periodate anions. It is the least abundant of the stable halogens, being the sixty-first most abundant element. As the heaviest essential mineral nutrient, iodine is required for the synthesis of thyroid hormones. Iodine deficiency affects about two billion people and is the leading preventable cause of intellectual disabilities. The dominant producers of iodine today are Chile and Japan. Due to its high atomic number and ease of attachment to organic compound ...
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Hafnium(IV) Iodide
Hafnium(IV) iodide is the inorganic compound with the formula HfI4. It is a red-orange, moisture sensitive, sublimable solid that is produced by heating a mixture of hafnium with excess iodine. It is an intermediate in the crystal bar process for producing hafnium metal. In this compound, the hafnium centers adopt octahedral coordination geometry. Like most binary metal halides, the compound is a polymeric. It is one-dimensional polymer consisting of chains of edge-shared bioctahedral Hf2I8 subunits, similar to the motif adopted by HfCl4. The nonbridging iodide ligands have shorter bonds to Hf than the bridging iodide ligands. References {{Iodides Iodides Hafnium compounds Metal halides ...
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Hafnium Tetrachloride
Hafnium(IV) chloride is the inorganic compound with the chemical formula, formula HfCl4. This colourless solid is the Precursor (chemistry), precursor to most hafnium organometallic compounds. It has a variety of highly specialized applications, mainly in materials science and as a catalyst. Preparation HfCl4 can be produced by several related procedures: *The reaction of carbon tetrachloride and hafnium oxide at above 450 °C; :HfO2 + 2 CCl4 → HfCl4 + 2 COCl2 *Chlorination of a mixture of HfO2 and charcoal, carbon above 600 °C using chlorine gas or sulfur monochloride: :HfO2 + 2 Cl2 + C → HfCl4 + CO2 *halogenation, Chlorination of hafnium carbide above 250 °C. Separation of Zr and Hf Hafnium and zirconium occur together in minerals such as zircon, cyrtolite and baddeleyite. Zircon contains 0.05% to 2.0% hafnium dioxide HfO2, cyrtolite with 5.5% to 17% HfO2 and baddeleyite contains 1.0 to 1.8 percent HfO2.Newnham, Ivan Edgar "Purification of H ...
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Zirconium Tetrabromide
Zirconium(IV) bromide is the inorganic compound with the formula ZrBr4. This colourless solid is the principal precursor to other Zr–Br compounds. Preparation and properties ZrBr4 is prepared by the action of bromine on zirconium oxide via a carbothermic reaction: : ZrO2 + 2C + 2Br2 → ZrBr4 + 2CO Like many related tetrahalides, it is purified by sublimation. It can also be prepared by treatment of the borohydride complex with hydrogen bromide: : Zr(BH4)4 + 4HBr → ZrBr4 + 4H2 + 2B2H6 Like related tetrabromides of Ti and Hf, ZrBr4 hydrolyzes readily to give oxy-bromide, with release of hydrogen bromide Hydrogen bromide is the inorganic compound with the formula . It is a hydrogen halide consisting of hydrogen and bromine. A colorless gas, it dissolves in water, forming hydrobromic acid, which is saturated at 68.85% HBr by weight at room temper .... Structure No single crystal X-ray study of ZrBr4 has been described. Some reports suggest that it is is ...
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Hafnium(IV) Bromide
Hafnium tetrabromide is the inorganic compound with the formula HfBr4. It is the most common bromide of hafnium. It is a colorless, diamagnetic moisture sensitive solid that sublimes in vacuum. It adopts a structure very similar to that of zirconium tetrabromide, featuring tetrahedral Hf centers, in contrast to the polymeric nature of hafnium tetrachloride Hafnium(IV) chloride is the inorganic compound with the chemical formula, formula HfCl4. This colourless solid is the Precursor (chemistry), precursor to most hafnium organometallic compounds. It has a variety of highly specialized applications, m ....Berdonosov, S. S.; Berdonosova, D. G.; Lapitskii, A. V.; Vlasov, L. G. "X-ray study of hafnium tetrabromide" Zhurnal Neorganicheskoi Khimii, 1963, vol. 8, 531-2. References {{Bromides Bromides Hafnium compounds Metal halides ...
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Halogenation
In chemistry, halogenation is a chemical reaction that entails the introduction of one or more halogens into a compound. Halide-containing compounds are pervasive, making this type of transformation important, e.g. in the production of polymers, drugs. This kind of conversion is in fact so common that a comprehensive overview is challenging. This article mainly deals with halogenation using elemental halogens (F2, Cl2, Br2, I2). Halides are also commonly introduced using salts of the halides and halogen acids. Many specialized reagents exist for and introducing halogens into diverse substrates, e.g. thionyl chloride. Organic chemistry Several pathways exist for the halogenation of organic compounds, including free radical halogenation, ketone halogenation, electrophilic halogenation, and halogen addition reaction. The nature of the substrate determines the pathway. The facility of halogenation is influenced by the halogen. Fluorine and chlorine are more electrophilic and are m ...
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Sulfur Monochloride
Disulfur dichloride is the inorganic compound of sulfur and chlorine with the formula S2Cl2. Some alternative names for this compound are ''sulfur monochloride'' (the name implied by its empirical formula, SCl), ''disulphur dichloride'' (British English Spelling) and ''sulphur monochloride'' (British English Spelling). S2Cl2 has the structure implied by the formula Cl−S−S−Cl, wherein the angle between the Cla−S−S and S−S−Clb planes is 90°. This structure is referred to as ''gauche'', and is akin to that for H2O2. A rare isomer of S2Cl2 is S=SCl2; this isomer forms transiently when S2Cl2 is exposed to UV-radiation (see thiosulfoxides). Synthesis, basic properties, reactions Pure disulfur dichloride is a yellow liquid that "smokes" in moist air due to reaction with water. An idealized (but complicated) equation is: :16 S2Cl2 + 16 H2O → 8 SO2 + 32 HCl + 3 S8 It is produced by partial chlorination of elemental sulfur. The reaction proceeds at usable rates at room ...
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Chlorine Gas
Chlorine is a chemical element with the symbol Cl and atomic number 17. The second-lightest of the halogens, it appears between fluorine and bromine in the periodic table and its properties are mostly intermediate between them. Chlorine is a yellow-green gas at room temperature. It is an extremely reactive element and a strong oxidising agent: among the elements, it has the highest electron affinity and the third-highest electronegativity on the revised Pauling scale, behind only oxygen and fluorine. Chlorine played an important role in the experiments conducted by medieval alchemists, which commonly involved the heating of chloride salts like ammonium chloride (sal ammoniac) and sodium chloride ( common salt), producing various chemical substances containing chlorine such as hydrogen chloride, mercury(II) chloride (corrosive sublimate), and hydrochloric acid (in the form of ). However, the nature of free chlorine gas as a separate substance was only recognised around 1630 ...
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