Powdered promethium oxide in a metal tray | |
Cubic form | |
Hexagonal form | |
Names | |
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IUPAC name Promethium(III) oxide | |
Other names Promethium sesquioxide | |
Identifiers | |
3D model (JSmol) | |
PubChem CID | |
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Properties | |
Pm2O3 | |
Molar mass | 337.824 g/mol |
Melting point | ~2320 °C [1] |
Structure | |
Cubic | |
Related compounds | |
Other anions | Promethium(III) chloride |
Other cations | Neodymium(III) oxide, Samarium(III) oxide, Neptunium(III) oxide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Promethium(III) oxide is a compound with the formula Pm2O3. It is the most common form of promethium.
Promethium oxide exists in three major crystalline forms: [1]
Form | Pearson symbol | Space group | No. | a,b,c (nm) | β(deg) | Z | Density (g/cm3) |
---|---|---|---|---|---|---|---|
Cubic | cI80 | Ia3 | 206 | 1.099 | 16 | 6.85 | |
Monoclinic | mS30 | C2/m | 12 | 1.422; 0.365; 0.891 | 100.1 | 6 | 7.48 |
Hexagonal | hP5 | P3m1 | 164 | 0.3802; 0.3802; 0.5954 | 1 | 7.62 |
*a, b and c are lattice parameters, Z is the number of formula units per unit cell, density is calculated from X-ray data.
The low-temperature cubic form converts to the monoclinic structure upon heating to 750–800 °C, and this transition can only be reversed by melting the oxide. The transition from the monoclinic to hexagonal form occurs at 1740 °C.
Promethium is a chemical element with symbol Pm and atomic number 61. All of its isotopes are radioactive; it is extremely rare, with only about 500–600 grams naturally occurring in the Earth's crust at any given time. Promethium is one of the only two radioactive elements that are both preceded and followed in the periodic table by elements with stable forms, the other being technetium. Chemically, promethium is a lanthanide. Promethium shows only one stable oxidation state of +3.
Bismuth(III) oxide is a compound of bismuth, and a common starting point for bismuth chemistry. It is found naturally as the mineral bismite (monoclinic) and sphaerobismoite, 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.
Non-stoichiometric compounds are chemical compounds, almost always solid inorganic compounds, having elemental composition whose proportions cannot be represented by a ratio of small natural numbers ; most often, in such materials, some small percentage of atoms are missing or too many atoms are packed into an otherwise perfect lattice work.
Vanadium(IV) oxide or vanadium dioxide is an inorganic compound with the formula VO2. It is a dark blue solid. Vanadium(IV) dioxide is amphoteric, dissolving in non-oxidising acids to give the blue vanadyl ion, [VO]2+ and in alkali to give the brown [V4O9]2− ion, or at high pH [VO4]4−. VO2 has a phase transition very close to room temperature (~68 °C (341 K)). Electrical resistivity, opacity, etc, can change by several orders of magnitude. Owing to these properties, it has been used in surface coating, sensors, and imaging. Potential applications include use in memory devices, phase-change switches, passive radiative cooling applications, such as smart windows and roofs, that cool or warm depending on temperature, aerospace communication systems and neuromorphic computing. It occurs in nature as the mineral paramontroseite.
Indium(III) sulfate (In2(SO4)3) is a sulfate salt of the metal indium. It is a sesquisulfate, meaning that the sulfate group occurs 11/2 times as much as the metal. It may be formed by the reaction of indium, its oxide, or its carbonate with sulfuric acid. An excess of strong acid is required, otherwise insoluble basic salts are formed. As a solid indium sulfate can be anhydrous, or take the form of a pentahydrate with five water molecules or a nonahydrate with nine molecules of water. Indium sulfate is used in the production of indium or indium containing substances. Indium sulfate also can be found in basic salts, acidic salts or double salts including indium alum.
Tungsten(IV) oxide is the chemical compound with the formula WO2. The bronze-colored solid crystallizes in a monoclinic cell. The rutile-like structure features distorted octahedral WO6 centers with alternate short W–W bonds (248 pm). Each tungsten center has the d2 configuration, which gives the material a high electrical conductivity.
Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C6H5)3, also written as Ph3PO or PPh3O (Ph = C6H5). It is one of the more common phosphine oxides. This colourless crystalline compound is a common but potentially useful waste product in reactions involving triphenylphosphine. It is a popular reagent to induce the crystallizing of chemical compounds.
ZSM-5, Zeolite Socony Mobil–5 (framework type MFI from ZSM-5 (five)), is an aluminosilicate zeolite belonging to the pentasil family of zeolites. Its chemical formula is NanAlnSi96–nO192·16H2O (0<n<27). Patented by Mobil Oil Company in 1975, it is widely used in the petroleum industry as a heterogeneous catalyst for hydrocarbon isomerization reactions.
Copper(I) sulfide is a copper sulfide, a chemical compound of copper and sulfur. It has the chemical compound Cu2S. It is found in nature as the mineral chalcocite. It has a narrow range of stoichiometry ranging from Cu1.997S to Cu2.000S. Samples are typically black.
Huttonite is a thorium nesosilicate mineral with the chemical formula ThSiO4 and which crystallizes in the monoclinic system. It is dimorphous with tetragonal thorite, and isostructual with monazite. An uncommon mineral, huttonite forms transparent or translucent cream–colored crystals. It was first identified in samples of beach sands from the West Coast region of New Zealand by the mineralogist Colin Osborne Hutton (1910–1971). Owing to its rarity, huttonite is not an industrially useful mineral.
Cerium nitrate refers to a family of nitrates of cerium in the +3 or +4 oxidation state. Often these compounds contain water, hydroxide, or hydronium ions in addition to cerium and nitrate. Double nitrates of cerium also exist.
Promethium(III) chloride is a chemical compound of promethium and chlorine with the formula PmCl3. It is an ionic, water soluble, crystalline salt that glows in the dark with a pale blue or green light due to promethium's intense radioactivity.
Titanium perchlorate is a molecular compound of titanium and perchlorate groups with formula Ti(ClO4)4. Anhydrous titanium perchlorate decomposes explosively at 130 °C and melts at 85 °C with a slight decomposition. It sublimes in a vacuum as low as 70 °C. Being a molecular with four perchlorate ligands, it is an unusual example of a transition metal perchlorate complex.
Promethium(III) nitrate is an inorganic compound, a salt of promethium and nitric acid with the chemical formula Pm(NO3)3. The compound is radioactive, soluble in water and forms crystalline hydrates.
Caesium enneabromodibismuthate is an inorganic compound with the formula Cs3Bi2Br9. It is one of the coordination complexes formed by caesium, bismuth and bromine. At room temperature, it is trigonal (P3m1) and it undergoes phase transformation to monoclinic phase (C12/c1) when the temperature is below 96 K.
Promethium(III) iodide is an inorganic compound, with the chemical formula of PmI3. It is a red radioactive solid with a melting point of 695 °C.
Promethium(III) bromide is an inorganic compound, with the chemical formula of PmBr3. It is radioactive salt. It is a crystal of the hexagonal crystal system, with the space group of P63/mc (No. 176).
Promethium compounds are compounds containing the element promethium, which normally take the +3 oxidation state. Promethium belongs to the cerium group of lanthanides and is chemically very similar to the neighboring elements. Because of its instability, chemical studies of promethium are incomplete. Even though a few compounds have been synthesized, they are not fully studied; in general, they tend to be pink or red in color. Treatment of acidic solutions containing Pm3+ ions with ammonia results in a gelatinous light-brown sediment of hydroxide, Pm(OH)3, which is insoluble in water. When dissolved in hydrochloric acid, a water-soluble yellow salt, PmCl3, is produced; similarly, when dissolved in nitric acid, a nitrate results, Pm(NO3)3. The latter is also well-soluble; when dried, it forms pink crystals, similar to Nd(NO3)3. The electron configuration for Pm3+ is [Xe] 4f4, and the color of the ion is pink. The ground state term symbol is 5I4. The sulfate is slightly soluble, like the other cerium group sulfates. Cell parameters have been calculated for its octahydrate; they lead to conclusion that the density of Pm2(SO4)3·8 H2O is 2.86 g/cm3. The oxalate, Pm2(C2O4)3·10 H2O, has the lowest solubility of all lanthanide oxalates.
Protactinium compounds are compounds containing the element protactinium. These compounds usually have protactinium in the +5 oxidation state, although these compounds can also exist in the +2, +3 and +4 oxidation states.
Promethium(III) oxalate is an oxalate of promethium, with the chemical formula Pm2(C2O4)3. Its decahydrate crystallizes in the monoclinic crystal system with space group P21/m. Promethium(III) oxalate trihydrate can decompose into stable basic carbonate Pm2O2CO3, and generate promethium(III) oxide at higher temperatures.