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Trioxide
A trioxide is a compound with three oxygen atoms. For metals with the M2O3 formula there are several common structures. Al2O3, Cr2O3, Fe2O3, and V2O3 adopt the corundum structure. Many rare earth oxides adopt the "A-type rare earth structure" which is hexagonal. Several others plus indium oxide adopt the " C-type rare earth structure", also called "bixbyite", which is cubic and related to the fluorite structure. List of trioxides MO3 *Carbon trioxide, CO3 *Chromium trioxide, CrO3 *Molybdenum trioxide, MoO3 *Rhenium trioxide, ReO3 * Selenium trioxide, SeO3 * Sulfur trioxide, SO3 *Tellurium trioxide, TeO3 *Tungsten trioxide, WO3 *Uranium trioxide, UO3 *Xenon trioxide, XeO3 M2O3 * Antimony trioxide, Sb2O3 *Arsenic trioxide, As2O3 *Bismuth(III) oxide, Bi2O3 *Boron trioxide, B2O3 *Cobalt(III) oxide, Co2O3 * Dichlorine trioxide, Cl2O3 *Dinitrogen trioxide, N2O3 * Gadolinium oxide, Gd2O3 *Gallium(III) oxide, Ga2O3 * Gold trioxide, Au2O3 *Indium(III) oxide, In2O3 * Iron(III) oxid ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Arsenic Trioxide
Arsenic trioxide, sold under the brand name Trisenox among others, is an inorganic compound and medication. As an industrial chemical, whose major uses include in the manufacture of wood preservatives, pesticides, and glass. As a medication, it is used to treat a type of cancer known as acute promyelocytic leukemia. For this use it is given by injection into a vein. Common side effects include vomiting, diarrhea, swelling, shortness of breath, and headaches. Severe side effects may include APL differentiation syndrome and heart problems. Use during pregnancy or breastfeeding may harm the baby. Arsenic trioxide has the formula . Its mechanism in treating cancer is not entirely clear. Arsenic trioxide was approved for medical use in the United States in 2000. It is on the World Health Organization's List of Essential Medicines. Approximately 50,000 tonnes are produced a year. Due to its toxicity, a number of countries have regulations around its manufacture and sale. Uses M ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Sulfur Trioxide
Sulfur trioxide (alternative spelling sulphur trioxide, also known as ''nisso sulfan'') is the chemical compound with the formula SO3. It has been described as "unquestionably the most important economically" sulfur oxide. It is prepared on an industrial scale as a precursor to sulfuric acid. Sulfur trioxide exists in several forms - gaseous monomer, crystalline trimer, and solid polymer. Sulfur trioxide is a solid at just below room temperature with a relatively narrow liquid range. Gaseous SO3 is the primary precursor to acid rain. Molecular structure and bonding Monomer The molecule SO3 is trigonal planar. As predicted by VSEPR theory, its structure belongs to the D3h point group. The sulfur atom has an oxidation state of +6 and may be assigned a formal charge value as low as 0 (if all three sulfur-oxygen bonds are assumed to be double bonds) or as high as +2 (if the Octet Rule is assumed). When the formal charge is non-zero, the S-O bonding is assumed to be delocalized. In a ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Uranium Trioxide
Uranium trioxide (UO3), also called uranyl oxide, uranium(VI) oxide, and uranic oxide, is the hexavalent oxide of uranium. The solid may be obtained by heating uranyl nitrate to 400 °C. Its most commonly encountered polymorph, γ-UO3, is a yellow-orange powder. Production and use There are three methods to generate uranium trioxide. As noted below, two are used industrially in the reprocessing of nuclear fuel and uranium enrichment. # U3O8 can be oxidized at 500 °C with oxygen. Note that above 750 °C even in 5 atm O2 UO3 decomposes into U3O8. # Uranyl nitrate, UO2(NO3)2·6H2O can be heated to yield UO3. This occurs during the reprocessing of nuclear fuel. Fuel rods are dissolved in HNO3 to separate uranyl nitrate from plutonium and the fission products (the PUREX method). The pure uranyl nitrate is converted to solid UO3 by heating at 400 °C. After reduction with hydrogen (with other inert gas present) to uranium dioxide, the uranium can be used in n ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dinitrogen Trioxide
Dinitrogen trioxide is the chemical compound with the formula N2O3. It is one of the simple nitrogen oxides. It forms upon mixing equal parts of nitric oxide and nitrogen dioxide and cooling the mixture below −21 °C (−6 °F): :NO + NO2 N2O3 Dinitrogen trioxide is only isolable at low temperatures, i.e. in the liquid and solid phases. In liquid and solid states, it has a deep blue color. At higher temperatures the equilibrium favors the constituent gases, with ''K''diss = 193 kPa (25 °C). This compound is sometimes called "nitrogen trioxide", but this name properly refers to another compound, the (uncharged) nitrate radical . Structure and bonding Typically, N–N bonds are similar in length to that in hydrazine (145 pm). Dinitrogen trioxide, however, has an unusually long N–N bond at 186 pm. Some other nitrogen oxides also possess long N–N bonds, including dinitrogen tetroxide (175 pm). The N2O3 molecule is planar and exhibits Cs symmet ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Chromium Trioxide
Chromium trioxide (also known as chromium(VI) oxide or chromic anhydride) is an inorganic compound with the formula CrO3. It is the acidic anhydride of chromic acid, and is sometimes marketed under the same name. This compound is a dark-purple solid under anhydrous conditions, bright orange when wet and which dissolves in water concomitant with hydrolysis. Millions of kilograms are produced annually, mainly for electroplating. Chromium trioxide is a powerful oxidiser and a carcinogen. Production, structure, and basic reactions Chromium trioxide is generated by treating sodium dichromate with sulfuric acid: :H2SO4 + Na2Cr2O7 → 2 CrO3 + Na2SO4 + H2O Approximately 100,000 tonnes are produced annually by this or similar routes. The solid consists of chains of tetrahedrally coordinated chromium atoms that share vertices. Each chromium center therefore shares two oxygen centers with neighbors. Two oxygen atoms are not shared, giving an overall stoichiometry of 1:3. : The s ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Tungsten Trioxide
Tungsten(VI) oxide, also known as tungsten trioxide is a chemical compound of oxygen and the transition metal tungsten, with formula WO3. The compound is also called tungstic anhydride, reflecting its relation to tungstic acid . It is a light yellow crystalline solid. Tungsten(VI) oxide occurs naturally in the form of hydrates, which include minerals: tungstite WO3·H2O, meymacite WO3·2H2O and hydrotungstite (of the same composition as meymacite, however sometimes written as H2WO4). These minerals are rare to very rare secondary tungsten minerals. History In 1841, a chemist named Robert Oxland gave the first procedures for preparing tungsten trioxide and sodium tungstate. He was granted patents for his work soon after, and is considered to be the founder of systematic tungsten chemistry. Structure and properties The crystal structure of tungsten trioxide is temperature dependent. It is tetragonal at temperatures above 740 °C, orthorhombic from 330 to 740 °C, monoclini ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Carbon Trioxide
Carbon trioxide (CO3) is an unstable oxide of carbon (an oxocarbon). The possible isomers of carbon trioxide include ones with molecular symmetry point groups ''Cs'', ''D3h'', and ''C2v.'' The ''C2v'' state, consisting of a dioxirane, has been shown to be the ground state of the molecule. Carbon trioxide should not be confused with the stable carbonate ion (). Carbon trioxide can be produced, for example, in the drift zone of a negative corona discharge by reactions between carbon dioxide (CO2) and the atomic oxygen (O) created from molecular oxygen by free electrons in the plasma. Another reported method is photolysis of ozone O3 dissolved in liquid CO2, or in CO2/ SF6 mixtures at −45 °C, irradiated with light of 253.7 nm. The formation of CO3 is inferred but it appears to decay spontaneously by the route :2 CO3 → 2 CO2 + O2 with a lifetime much shorter than 1 minute. Carbon trioxide can be made by blowing ozone at dry ice (solid CO2), and it has also been det ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Xenon Trioxide
Xenon trioxide is an unstable compound of xenon in its +6 oxidation state. It is a very powerful oxidizing agent, and liberates oxygen from water slowly, accelerated by exposure to sunlight. It is dangerously explosive upon contact with organic materials. When it detonates, it releases xenon and oxygen gas. Chemistry Xenon trioxide is a strong oxidising agent and can oxidise most substances that are at all oxidisable. However, it is slow-acting and this reduces its usefulness. Above 25 °C, xenon trioxide is very prone to violent explosion: :2 XeO3 → 2 Xe + 3 O2 (Δ''H''f = −403 kJ/ mol) When it dissolves in water, an acidic solution of xenic acid is formed: :XeO3(aq) + H2O → H2XeO4 H+ + This solution is stable at room temperature and lacks the explosive properties of xenon trioxide. It oxidises carboxylic acids quantitatively to carbon dioxide and water. Alternatively, it dissolves in alkaline solutions to form ''xenates''. The anion is the predominant specie ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Molybdenum Trioxide
Molybdenum trioxide describes a family of inorganic compounds with the formula MoO3(H2O)n where n = 0, 1, 2. These compounds are produced on the largest scale of any molybdenum compound. The anhydrous oxide is a precursor to molybdenum metal, an important alloying agent. It is also an important industrial catalyst. It is a yellow solid, although impure samples can appear blue or green. Molybdenum trioxide occurs as the rare mineral molybdite. Structure In the gas phase, three oxygen atoms are bonded to the central molybdenum atom. In the solid state, anhydrous MoO3 is composed of layers of distorted MoO6 octahedra in an orthorhombic crystal. The octahedra share edges and form chains which are cross-linked by oxygen atoms to form layers. The octahedra have one short molybdenum-oxygen bond to a non-bridging oxygen. Also known is a metastable (β) form of MoO3 with a WO3-like structure. Preparation and principal reactions MoO3 is produced industrially by roasting molybdenum ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Bismuth(III) Oxide
Bismuth(III) oxide is perhaps the most industrially important compound of bismuth. It is also a common starting point for bismuth chemistry. It is found naturally as the mineral bismite (monoclinic) and sphaerobismoite (tetragonal, much more rare), but it is usually obtained as a by-product of the smelting of copper and lead ores. Dibismuth trioxide is commonly used to produce the " Dragon's eggs" effect in fireworks, as a replacement of red lead. Structure The structures adopted by differ substantially from those of arsenic(III) oxide, , and antimony(III) oxide, .Wells, A.F. (1984) ''Structural Inorganic Chemistry''. 5th. London, England: Oxford University Press. p.890 Bismuth oxide, has five crystallographic polymorphs. The room temperature phase, α- has a monoclinic crystal structure. There are three high temperature phases, a tetragonal β-phase, a body-centred cubic γ-phase, a cubic δ- phase and an ε-phase. The room temperature α-phase has a complex structure with ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phosphorus Trioxide
Phosphorus trioxide is the chemical compound with the molecular formula P4O6. Although the molecular formula suggests the name tetraphosphorus hexaoxide, the name phosphorus trioxide preceded the knowledge of the compound's molecular structure, and its usage continues today. This colorless solid is structurally related to adamantane. It is formally the anhydride of phosphorous acid, H3PO3, but cannot be obtained by the dehydration of the acid. A white solid that melts at room temperature, it is waxy, crystalline and highly toxic, with garlic odour. Preparation It is obtained by the combustion of phosphorus in a limited supply of air at low temperatures. :P4 + 3 O2 → P4O6 By-products include red phosphorus suboxide. Chemical properties Phosphorus trioxide reacts with water to form phosphorous acid, reflecting the fact that it is the anhydride of that acid. : P4O6 + 6 H2O → 4 H3PO3 It reacts with hydrogen chloride to form H3PO3 and phosphorus trichloride. : P4O6 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Rhenium Trioxide
Rhenium trioxide or rhenium(VI) oxide is an inorganic compound with the formula ReO3. It is a red solid with a metallic lustre that resembles copper in appearance. It is the only stable trioxide of the Group 7 elements ( Mn, Tc, Re). Preparation and structure Rhenium trioxide can be formed by reducing rhenium(VII) oxide with carbon monoxide at 200 °C or elemental rhenium at 400 °C. :Re2O7 + CO → 2 ReO3 + CO2 :3 Re2O7 + Re → 7 ReO3 Re2O7 can also be reduced with dioxane. Rhenium trioxide crystallizes with a primitive cubic unit cell, with a lattice parameter of 3.742 Å (374.2 pm). The structure of ReO3 is similar to that of perovskite (ABO3), without the large A cation at the centre of the unit cell. Each rhenium center is surrounded by an octahedron defined by six oxygen centers. These octahedra share corners to form the 3-dimensional structure. The coordination number of O is 2, because each oxygen atom has 2 neighbouring Re atoms., p. 1 ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
