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{{chembox
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| verifiedrevid = 435546139
|  Name = Arsenic pentoxide
|  ImageFile = Arsenic-pentoxide-3D-polyhedra.png
|  ImageName = Arsenic pentoxide
|  OtherNames = Arsenic(V) oxide<br />Arsenic oxide<br />Arsenic anhydride
| Section1 = {{Chembox Identifiers
|  InChI = 1/As2O5/c3-1(4)7-2(5)6
| SMILES = O=[As](=O)O[As](=O)=O
| InChIKey = COHDHYZHOPQOFD-UHFFFAOYAN
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/As2O5/c3-1(4)7-2(5)6
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = COHDHYZHOPQOFD-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 1303-28-2
|  PubChem = 14771
|  EINECS = 215-116-9
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 14088
|  RTECS = CG2275000
  }}
| Section2 = {{Chembox Properties
|  Formula = As<sub>2</sub>O<sub>5</sub>
|  MolarMass = 229.8402 g/mol
|  Appearance = white [[hygroscopic]] powder
|  Density = 4.32 g/cm<sup>3</sup>
|  MeltingPt = 315 °C (decomposes)
|  BoilingPt =
|  Solubility = 59.5 g/100 mL (0 °C) <br> 65.8 g/100 mL (20 °C) <br> 8.20 g/100 mL (100 °C)
|  SolubleOther = soluble in [[alcohol]]
|  pKa = 7
  }}
| Section7 = {{Chembox Hazards
|  ExternalMSDS =
|  EUClass = Very toxic ('''T+''')<br />Carc. Cat. 1<br />Dangerous for the environment ('''N''')
|  NFPA-H = 4
|  NFPA-F = 0
|  NFPA-R = 0
|  RPhrases = {{R45}}, {{R23/25}}, {{R50/53}}
|  SPhrases = {{S53}}, {{S45}}, {{S60}}, {{S61}}
|  LD50 = 8 mg/kg (rat, oral)
  }}
| Section8 = {{Chembox Other
|  OtherAnions =
|  OtherCations = [[Phosphorus pentoxide]]<br />[[Antimony pentoxide]]
|  OtherCpds = [[Arsenic trioxide]]<br />[[Arsenic acid]]}}
}}
 
'''Arsenic pentoxide''' is the [[inorganic compound]] with the formula As<sub>2</sub>O<sub>5</sub>.<ref>{{Greenwood&Earnshaw2nd}}</ref>  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]] (As<sub>2</sub>O<sub>3</sub>). All arsenic compounds are highly toxic and thus find only limited commercial applications.
 
==Structure==
The structure consists of tetrahedral {AsO<sub>4</sub>} and octahedral {AsO<sub>6</sub>} centres linked by sharing corners.<ref name = "Jansen">{{cite journal | author = Martin Jansen | title = Crystal Structure of As<sub>2</sub>O<sub>5</sub> | year = 1977 | journal = Angewandte Chemie International Edition in English | volume = 16 | issue = 5 | pages = 314–315 | doi = 10.1002/anie.197703142}}</ref>    The structure differs from that of the corresponding phosphorus(V) oxide.
 
==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.<ref name = "Mellor">{{cite journal | author = J. W. Mellor | title = Comprehensive Treatise on Inorganic & Theoretical Chemistry | journal = http://www.rexresearch.com/alchemy10/melloras.htm English | volume = IX - Arsenic }}</ref>  [[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.<ref name = "Zenger">{{cite journal | author = C.W. Zenger et al | title = Arsenic 149 | journal = http://tera-3.ul.cs.cmu.edu/NASD/4dcb85c3-9fee-4c83-9e6d-fe6ce5522b59/China/disk4/75/75-2/31005153/HTML/00000166.htm}}</ref>  The water in the alkalies evaporated at 180˚C, and the arsenic pentoxide was stable below 400˚C .<ref name = "Mellor"/>
 
===Modern methods===
Arsenic pentoxide can be crystallized by heating As<sub>2</sub>O<sub>3</sub> under oxygen. This reaction is reversible:<ref name = "Jansen"/>
 
As<sub>2</sub>O<sub>5</sub> <math>\overrightarrow{\leftarrow}</math>  As<sub>2</sub>O<sub>3</sub> + O<sub>2</sub>
 
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:<ref name=Ullmann>{{Ullmann | author = Grund, S. C.; Hanusch, K.; Wolf, H. U. | title = Arsenic and Arsenic Compounds | doi = 10.1002/14356007.a03_113.pub2 }}</ref>
2 As<sub>2</sub>S<sub>3</sub>  +  11 O<sub>2</sub>  →  2 As<sub>2</sub>O<sub>5</sub> + 6 SO<sub>2</sub>
 
==Safety==
{{main|arsenic toxicity}}
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==
<references/>
 
==External links==
*[http://www.cdc.gov/niosh/npg/npgd0038.html NIOSH Pocket Guide to Chemical Hazards]
*[http://www-cie.iarc.fr/htdocs/monographs/suppl7/arsenic.html IARC Monograph &ndash; Arsenic and Arsenic Compounds]
*[http://ntp.niehs.nih.gov/ntp/roc/eleventh/profiles/s015arse.pdf NTP Report on Carcinogens &ndash; Inorganic Arsenic Compounds]
*[http://esis.jrc.ec.europa.eu/ ESIS: European chemical Substances Information System]
*{{nist}}
 
{{Arsenic compounds}}
 
{{DEFAULTSORT:Arsenic Pentoxide}}
[[Category:Arsenic compounds]]
[[Category:Chalcoarsenics]]
[[Category:Oxides]]
[[Category:IARC Group 1 carcinogens]]

Latest revision as of 10:12, 15 May 2014

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