Arsenic pentoxide

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Arsenic pentoxide
Arsenic pentoxide
Names
Other names
Arsenic(V) oxide
Arsenic oxide
Arsenic anhydride
Identifiers
1303-28-2 YesY
ChemSpider 14088 YesY
EC Number 215-116-9
Jmol 3D model Interactive image
PubChem 14771
RTECS number CG2275000
  • InChI=1S/As2O5/c3-1(4)7-2(5)6 YesY
    Key: COHDHYZHOPQOFD-UHFFFAOYSA-N YesY
  • InChI=1/As2O5/c3-1(4)7-2(5)6
    Key: COHDHYZHOPQOFD-UHFFFAOYAN
  • O=[As](=O)O[As](=O)=O
Properties
As2O5
Molar mass 229.8402 g/mol
Appearance white hygroscopic powder
Density 4.32 g/cm3
Melting point 315 °C (599 °F; 588 K) (decomposes)
59.5 g/100 mL (0 °C)
65.8 g/100 mL (20 °C)
8.20 g/100 mL (100 °C)
Solubility soluble in alcohol
Acidity (pKa) 7
Vapor pressure {{{value}}}
Related compounds
Other cations
Phosphorus pentoxide
Antimony pentoxide
Related compounds
Arsenic trioxide
Arsenic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Arsenic pentoxide is the inorganic compound with the formula As2O5.[1] This glassy, white, deliquescent solid is relatively unstable, consistent with the rarity of the As(V) oxidation state. More common, and far more important commercially, is arsenic(III) oxide (As2O3). All arsenic compounds are highly toxic and thus find only limited commercial applications.

Structure

The structure consists of tetrahedral {AsO4} and octahedral {AsO6} centres linked by sharing corners.[2] The structure differs from that of the corresponding phosphorus(V) oxide; as a result, although there is still a solid solution with that oxide, it only progresses to the equimolar point, at which point phosphorus has substituted for arsenic in all of its tetrahedral sites. Likewise, arsenic pentoxide can also dissolve up to an equimolar amount of antimony pentoxide, as antimony substitutes for arsenic only in its octahedral sites.[3]

Synthesis

Historical

Paracelsus Macquer found a crystallizable salt which he called ‘sel neutre arsenical’. This salt was the obtaining residue after distilling nitric acid from a mixture of potassium nitrate and arsenic trioxide. Previously Paracelsus heated a mixture of arsenic trioxide and potassium nitrate. He applied the term ‘arsenicum fixum’ to the product. A. Libavius called the same product ‘butyrum arsenici’ (butter of arsenic), although this term was actually used for arsenic tricholoride. The products that Paracelsus and Libavius found were all impure alkali arsenates.[4] Scheele prepared a number of arsenates by the action of arsenic acid on the alkalies. One of the arsenates that he prepared, was arsenic pentoxide.[5] The water in the alkalies evaporated at 180˚C, and the arsenic pentoxide was stable below 400˚C .[4]

Modern methods

Arsenic pentoxide can be crystallized by heating As2O3 under oxygen. This reaction is reversible:[2]

As2O5 \overrightarrow{\leftarrow} As2O3 + O2

Strong oxidizing agents such as ozone, hydrogen peroxide, and nitric acid convert arsenic trioxide to the pentoxide.

Arsenic acid can be generated via routine processing of arsenic compounds including the oxidation of arsenic and arsenic-containing minerals in air. Illustrative is the roasting of orpiment, a typical arsenic sulfide ore:[6] 2 As2S3 + 11 O2 → 2 As2O5 + 6 SO2

Safety

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Like all arsenic compounds, the pentoxide is highly toxic. Its reduced derivative arsenite, which is an As(III) compound, is even more toxic since it has a high affinity for thiol groups of cysteine residues in proteins.

References

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External links