Plutonium borides

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Structure of PuB2: boron atoms shown red in hexagonally bonded network; metal atoms shown green in interleaving layers Magnesium-diboride-3D-balls.png
Structure of PuB2: boron atoms shown red in hexagonally bonded network; metal atoms shown green in interleaving layers
Structure of PuB6 (boron atoms in octahedral groups shown red with plutonium atoms shown blue at cubical vertices; bonding depiction is naive) CaHexaboride.jpg
Structure of PuB6 (boron atoms in octahedral groups shown red with plutonium atoms shown blue at cubical vertices; bonding depiction is naïve)

Several plutonium borides can be formed by direct combination of plutonium and boron powders in an inert atmosphere at reduced pressure.

PuB was reported to form at 1200 °C with a range of 40–70% boron. It supposedly has a Pu-B bond length of 2.46 Å and the NaCl structure, as do TiB, ZrB and HfB. [1] The existence of PuB was contested later based on several arguments. [2]

PuB2 is formed at 800 °C and has a similar structure to most other metal diborides.

At 1200 °C with 70–85% boron, mixtures of PuB4 and PuB6 are formed, with more of the latter as the temperature increases; PuB4 has the tetragonal structure (same as UB4), and PuB6 has cubic structure, same as all hexaborides (CaB6, LaB6 etc.). [1]

The most remarkable plutonium boride is arguably PuB100. Its existence [2] demonstrates the importance of contamination in boride research because as little as 1% of an impurity is capable of changing its crystal structure.

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<span class="mw-page-title-main">Boron nitride</span> Refractory compound of boron and nitrogen with formula BN

Boron nitride is a thermally and chemically resistant refractory compound of boron and nitrogen with the chemical formula BN. It exists in various crystalline forms that are isoelectronic to a similarly structured carbon lattice. The hexagonal form corresponding to graphite is the most stable and soft among BN polymorphs, and is therefore used as a lubricant and an additive to cosmetic products. The cubic variety analogous to diamond is called c-BN; it is softer than diamond, but its thermal and chemical stability is superior. The rare wurtzite BN modification is similar to lonsdaleite but slightly softer than the cubic form.

<span class="mw-page-title-main">Boron</span> Chemical element, symbol B and atomic number 5

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<span class="mw-page-title-main">Crystal structure of boron-rich metal borides</span> Boron chemical complexes

Metals, and specifically rare-earth elements, form numerous chemical complexes with boron. Their crystal structure and chemical bonding depend strongly on the metal element M and on its atomic ratio to boron. When B/M ratio exceeds 12, boron atoms form B12 icosahedra which are linked into a three-dimensional boron framework, and the metal atoms reside in the voids of this framework. Those icosahedra are basic structural units of most allotropes of boron and boron-rich rare-earth borides. In such borides, metal atoms donate electrons to the boron polyhedra, and thus these compounds are regarded as electron-deficient solids.

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<span class="mw-page-title-main">Chromium(III) boride</span> Chemical compound

Chromium(III) boride, also known as chromium monoboride (CrB), is an inorganic compound with the chemical formula CrB. It is one of the six stable binary borides of chromium, which also include Cr2B, Cr5B3, Cr3B4, CrB2, and CrB4. Like many other transition metal borides, it is extremely hard (21-23 GPa), has high strength (690 MPa bending strength), conducts heat and electricity as well as many metallic alloys, and has a high melting point (~2100 °C). Unlike pure chromium, CrB is known to be a paramagnetic, with a magnetic susceptibility that is only weakly dependent on temperature. Due to these properties, among others, CrB has been considered as a candidate material for wear resistant coatings and high-temperature diffusion barriers.

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Iron boride refers to various inorganic compounds with the formula FexBy. Two main iron borides are FeB and Fe2B. Some iron borides possess useful properties such as magnetism, electrical conductivity, corrosion resistance and extreme hardness. Some iron borides have found use as hardening coatings for iron. Iron borides have properties of ceramics such as high hardness, and properties of metal properties, such as thermal conductivity and electrical conductivity. Boride coatings on iron are superior mechanical, frictional, and anti-corrosive. Iron monoboride (FeB) is a grey powder that is insoluble in water. FeB is harder than Fe2B, but is more brittle and more easily fractured upon impact.

<span class="mw-page-title-main">Thorium compounds</span> Chemical compounds

Many compounds of thorium are known: this is because thorium and uranium are the most stable and accessible actinides and are the only actinides that can be studied safely and legally in bulk in a normal laboratory. As such, they have the best-known chemistry of the actinides, along with that of plutonium, as the self-heating and radiation from them is not enough to cause radiolysis of chemical bonds as it is for the other actinides. While the later actinides from americium onwards are predominantly trivalent and behave more similarly to the corresponding lanthanides, as one would expect from periodic trends, the early actinides up to plutonium have relativistically destabilised and hence delocalised 5f and 6d electrons that participate in chemistry in a similar way to the early transition metals of group 3 through 8: thus, all their valence electrons can participate in chemical reactions, although this is not common for neptunium and plutonium.

Samarium compounds are compounds formed by the lanthanide metal samarium (Sm). In these compounds, samarium generally exhibits the +3 oxidation state, such as SmCl3, Sm(NO3)3 and Sm(C2O4)3. Compounds with samarium in the +2 oxidation state are also known, for example SmI2.

Americium compounds are compounds containing the element americium (Am). These compounds can form in the +2, +3, and +4, although the +3 oxidation state is the most common. The +5, +6 and +7 oxidation states have also been reported.

References

  1. 1 2 B. J. McDonald; W. I. Stuart (1960). "The crystal structures of some plutonium borides". Acta Crystallogr. 13 (5): 447–448. Bibcode:1960AcCry..13..447M. doi: 10.1107/S0365110X60001059 .
  2. 1 2 H. A. Eick (1965). "Plutonium Borides". Inorganic Chemistry. 4 (8): 1237–1239. doi:10.1021/ic50030a037.