User:Mac239/Arsenate

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Article Draft arsenate[edit]

Lead[edit]

The arsenate ion has the formula .[1] Bonding in arsenate consists of a central arsenic atom, with oxidation state +5, double bonded to one oxygen atom and single bonded to a further three oxygen atoms.[2] The four oxygen atoms orient around the arsenic atom in a tetrahedral geometry.[2] The ion's 3- charge is dispersed across all four oxygen atoms through resonance.

Arsenate readily reacts with metals to form arsenate metal compounds.[2] Arsenate is a moderate oxidizer and an electron acceptor, with an electrode potential of +0.56 V for its reduction to arsenite.[3] Due to arsenic having the same valency and similar atomic radius to phosphorus, arsenate shares similar geometry and reactivity with phosphate.[4] Arsenate can replace phosphate in biochemical reactions and is toxic to most organisms.[4][5]

Article body[edit]

Speciation[edit]

Depending on the pH, arsenate can be found as arsenic acid () dihydrogen arsenate (), hydrogen arsenate (), or arsenate ().[4] Trihydrogen arsenate is also known as arsenic acid. At a given pH, the distribution of these arsenate species can be determined from their respective acid dissociation constants.

Pourbaix diagram showing the distribution of arsenate and arsenite species in water. Oxygenated waters have a high pe value and arsenate species dominate while in deoxygenated water, with low pe, arsenite species dominate.
H3AsO4 + H2O ⇌ H
2
AsO
4
+ H3O+ (log K1 = −2.19)
H
2
AsO
4
+ H2O ⇌ HAsO2−
4
+ H3O+ (log K2 = −6.94)
HAsO2−
4
+ H2O ⇌ AsO3−
4
+ H3O+H (log K3 = −11.5)

These values are similar to those of phosphoric acid. Hydrogen arsenate and dihydrogen arsenate predominate in aqueous solution near neutral pH.

Uses[edit]

Arsenate based pesticides such as lead hydrogen arsenate were commonly used until their replacement by newer pesticides such as DDT and subsequent ban by multiple regulatory bodies due to health concerns.[6][7]

Cobalt violet pigment[8][9][10]

Egyptian blue pigment[11]

Chromated copper arsenate wood[12]

Contamination[edit]

Water; rivers[13]

Food; honey[14]

Occurrence[edit][edit]

Adamite, one of the many arsenate minerals that occur naturally.

Arsenates occur naturally, in hydrated and anhydrous form, in a variety of minerals. Examples of arsenate-containing minerals include adamite, alarsite, annabergite, erythrite and legrandite.[15] Where two arsenate ions are required to balance the charge in a formula, it is called diarsenate for example zinc diarsenate, Zn3(AsO4)2.

Arsenate poisoning[edit][edit]

Arsenate is harmful to humans and animals as it interferes with the normal functioning of glycolysis and the Krebs cycle. Arsenate replaces inorganic phosphate in the step of glycolysis that produces 1,3-bisphosphoglycerate from glyceraldehyde 3-phosphate. This yields 1-arseno-3-phosphoglycerate instead, which is unstable and quickly hydrolyzes, forming the next intermediate in the pathway, 3-phosphoglycerate. Therefore, glycolysis proceeds, but the ATP molecule that would be generated from 1,3-bisphosphoglycerate is lost – arsenate is an uncoupler of glycolysis, explaining its toxicity.[16][17]

As with other arsenic compounds, arsenate binds to lipoic acid, inhibiting the conversion of pyruvate into acetyl-CoA, blocking the Krebs cycle and therefore resulting in further loss of ATP.[17]

References[edit]

  1. ^ PubChem. "Arsenate ion". pubchem.ncbi.nlm.nih.gov. Retrieved 2023-04-02.
  2. ^ a b c "Arsenate mineral | Britannica". www.britannica.com. Retrieved 2023-04-02.
  3. ^ "P1: Standard Reduction Potentials by Element". Chemistry LibreTexts. 2013-12-02. Retrieved 2023-03-29.
  4. ^ a b c Pollutants, National Research Council (US) Committee on Medical and Biological Effects of Environmental (1977). Chemistry of Arsenic. National Academies Press (US).
  5. ^ Elias, Mikael; Wellner, Alon; Goldin-Azulay, Korina; Chabriere, Eric; Vorholt, Julia A.; Erb, Tobias J.; Tawfik, Dan S. (2012-11). "The molecular basis of phosphate discrimination in arsenate-rich environments". Nature. 491 (7422): 134–137. doi:10.1038/nature11517. ISSN 1476-4687. {{cite journal}}: Check date values in: |date= (help)
  6. ^ "The Evolution of Chemical Pesticides". www.fishersci.ca. Retrieved 2023-04-02.
  7. ^ "The Global Problem of Lead Arsenate Pesticide". lead.org.au. Retrieved 2023-04-02.
  8. ^ Corbeil, Marie-Claude; Charland, Jean-Pierre; Moffatt, Elizabeth A. (2002). "The Characterization of Cobalt Violet Pigments". Studies in Conservation. 47 (4): 237–249. doi:10.2307/1506784. ISSN 0039-3630.
  9. ^ "Cobalt violet". ColourLex. Retrieved 2023-04-10.
  10. ^ "Cobaltous arsenate - CAMEO". cameo.mfa.org. Retrieved 2023-04-10.
  11. ^ Dariz, Petra; Schmid, Thomas (2021-05-28). "Trace compounds in Early Medieval Egyptian blue carry information on provenance, manufacture, application, and ageing". Scientific Reports. 11 (1): 11296. doi:10.1038/s41598-021-90759-6. ISSN 2045-2322.
  12. ^ Barton, C. (2014-01-01), Wexler, Philip (ed.), "CCA-Treated Wood", Encyclopedia of Toxicology (Third Edition), Oxford: Academic Press, pp. 751–752, ISBN 978-0-12-386455-0, retrieved 2023-04-10
  13. ^ Sánchez-Rodas, Daniel; Luis Gómez-Ariza, José; Giráldez, Inmaculada; Velasco, Alfredo; Morales, Emilio (2005-06-01). "Arsenic speciation in river and estuarine waters from southwest Spain". The Science of the Total Environment. 345 (1–3): 207–217. doi:10.1016/j.scitotenv.2004.10.029. ISSN 0048-9697. PMID 15919540.
  14. ^ Zarić, Nenad M.; Braeuer, Simone; Goessler, Walter (2022-06-15). "Arsenic speciation analysis in honey bees for environmental monitoring". Journal of Hazardous Materials. 432: 128614. doi:10.1016/j.jhazmat.2022.128614. ISSN 0304-3894.
  15. ^ "The mineralogy of Arsenic". Mindat.org.{{cite web}}: CS1 maint: url-status (link)
  16. ^ "How does arsenic kill?". livescience.com. Retrieved 2023-03-31.
  17. ^ a b Hughes, Michael F. (2002-07-07). "Arsenic toxicity and potential mechanisms of action". Toxicology Letters. 133 (1): 1–16. doi:10.1016/s0378-4274(02)00084-x. ISSN 0378-4274. PMID 12076506.