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Phosphate

Names
Systematic IUPAC name Phosphate
Identifiers
CAS Number	14265-44-2
3D model (JSmol)	Interactive image Interactive image Interactive image Interactive image
Beilstein Reference	3903772
ChEBI	CHEBI:18367
ChemSpider	1032
Gmelin Reference	1997
MeSH	Phosphates
PubChem CID	1061
UNII	NK08V8K8HR
InChI InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3Key: NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES P()()=O P(=O)() O=P()() ()()
Properties
Chemical formula	PO 4
Molar mass	94.9714 g mol
Conjugate acid	Hydrogen phosphate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is  ?) Infobox references

A Phosphate is a chemical derivative of phosphoric acid. The phosphate ion (PO
₄)
is an inorganic chemical, the conjugate base that can form many different salts. In organic chemistry, a phosphate, or organophosphate, is an ester of phosphoric acid of the various phosphoric acids and phosphates, organic phosphates are important in biochemistry and biogeochemistry (and, consequently, in ecology), and inorganic phosphates are mined to obtain phosphorus for use in agriculture and industry. At elevated temperatures in the solid state, phosphates can condense to form pyrophosphates.

In biology, adding phosphates to—and removing them from—proteins in cells are both pivotal in the regulation of metabolic processes. Referred to as phosphorylation and dephosphorylation, respectively, they are important ways that energy is stored and released in living systems.

Chemical properties

The phosphate ion is a polyatomic ion with the empirical formula (PO
₄)
and a molar mass of 94.97 g/mol. It consists of one central phosphorus atom surrounded by four oxygen atoms in a tetrahedral arrangement. The phosphate ion carries a −3 formal charge and is the conjugate base of the hydrogen phosphate ion, H(PO
₄)
, which is the conjugate base of H
₂(PO
₄)
, the dihydrogen phosphate ion, which in turn is the conjugate base of phosphoric acid, H
₃PO
₄. A phosphate salt forms when a positively charged ion attaches to the negatively charged oxygen atoms of the ion, forming an ionic compound.

Many phosphates are not soluble in water at standard temperature and pressure. The sodium, potassium, rubidium, caesium, and ammonium phosphates are all water-soluble. Most other phosphates are only slightly soluble or are insoluble in water. As a rule, the hydrogen and dihydrogen phosphates are slightly more soluble than the corresponding phosphates. The pyrophosphates are mostly water-soluble. Aqueous phosphate exists in four forms:

• In strongly basic conditions, the phosphate ion, (PO
  ₄)
  , predominates.
• In weakly basic conditions, the hydrogen phosphate ion, H(PO
  ₄)
  , is prevalent.
• In weakly acidic conditions, the dihydrogen phosphate ion, H
  ₂(PO
  ₄)
  , is most common.
• In strongly acidic conditions, trihydrogen phosphate, H
  ₃PO
  ₄, phosphoric acid, is the main form.

• H
  ₃PO
  ₄
  Phosphoric acid
• H
  ₂(PO
  ₄)
  
  Dihydrogen phosphate
• H(PO
  ₄)
  
  Hydrogen phosphate
• (PO
  ₄)
  
  Phosphate ion

More precisely, considering these three equilibrium reactions:

H
₃PO
₄ ⇌ H + H
₂(PO
₄)

H
₂(PO
₄)
⇌ H + H(PO
₄)

H(PO
₄)
⇌ H + (PO
₄)

the corresponding constants at 25 °C (in mol/L) are (see phosphoric acid):

${\displaystyle K_{\mathrm {a1} }={\frac {}{}}\simeq 7.5\times 10^{-3}}$      (pK_a1 ≈ 2.12)

${\displaystyle K_{\mathrm {a2} }={\frac {}{}}\simeq 6.2\times 10^{-8}}$      (pK_a2 ≈ 7.21)

${\displaystyle K_{\mathrm {a3} }={\frac {}{}}\simeq 2.14\times 10^{-13}}$      (pK_a3 ≈ 12.67)

Speciation

The speciation diagram obtained using these pK values shows three distinct regions. In effect, H
₃PO
₄, H
₂(PO
₄)
and H(PO
₄)
behave as separate weak acids because the successive pK values differ by more than 4. For each acid, the pH at half-neutralization is equal to the pK value of the acid. The region in which the acid is in equilibrium with its conjugate base is defined by pH ≈ pK ± 2. Thus, the three pH regions are approximately 0–4, 5–9 and 10–14. This is a simplified model, assuming a constant ionic strength. It will not hold in reality at very low and very high pH values.

For a neutral pH, as in the cytosol, pH = 7.0

${\displaystyle {\frac {}{}}\simeq 7.5\times 10^{4}{\mbox{ , }}{\frac {}{}}\simeq 0.62{\mbox{ , }}{\frac {}{}}\simeq 2.14\times 10^{-6}}$

so that only H
₂(PO
₄)
and H(PO
₄)
ions are present in significant amounts (62% H
₂(PO
₄)
, 38% H(PO
₄)
. Note that in the extracellular fluid (pH = 7.4), this proportion is inverted (61% H(PO
₄)
, 39% H
₂(PO
₄)
).

Phosphate can form many polymeric ions such as pyrophosphate), (P
₂O
₇)
, and triphosphate, (P
₃O
₁₀)
. The various metaphosphate ions (which are usually long linear polymers) have an empirical formula of (PO
₃)
and are found in many compounds.

Biochemistry of phosphates

In biological systems, phosphorus is found as a free phosphate ion in solution and is called inorganic phosphate, to distinguish it from phosphates bound in various phosphate esters. Inorganic phosphate is generally denoted P_i and at physiological (homeostatic) pH primarily consists of a mixture of H(PO
₄)
and H
₂(PO
₄)
ions.

Inorganic phosphate can be created by the hydrolysis of pyrophosphate, denoted PP_i:

(P
₂O
₇)
+ H₂O ⇌ 2 H(PO
₄)

However, phosphates are most commonly found in the form of adenosine phosphates (AMP, ADP, and ATP) and in DNA and RNA. It can be released by the hydrolysis of ATP or ADP. Similar reactions exist for the other nucleoside diphosphates and triphosphates. Phosphoanhydride bonds in ADP and ATP, or other nucleoside diphosphates and triphosphates, can release high amounts of energy when hydrolyzed which give them their vital role in all living organisms. They are generally referred to as high-energy phosphate, as are the phosphagens in muscle tissue. Compounds such as substituted phosphines have uses in organic chemistry, but do not seem to have any natural counterparts.

The addition and removal of phosphate from proteins in all cells is a pivotal strategy in the regulation of metabolic processes. Phosphorylation and dephosphorylation are important ways that energy is stored and released in living systems. Cells use ATP for this.

Phosphate is useful in animal cells as a buffering agent. Phosphate salts that are commonly used for preparing buffer solutions at cell pHs include Na₂HPO₄, NaH₂PO₄, and the corresponding potassium salts.

An important occurrence of phosphates in biological systems is as the structural material of bone and teeth. These structures are made of crystalline calcium phosphate in the form of hydroxyapatite. The hard dense enamel of mammalian teeth consists of fluoroapatite, a hydroxy calcium phosphate where some of the hydroxyl groups have been replaced by fluoride ions.

Plants take up phosphorus through several pathways: the arbuscular mycorrhizal pathway and the direct uptake pathway.

Occurrence and mining

Phosphates are the naturally occurring form of the element phosphorus, found in many phosphate minerals. In mineralogy and geology, phosphate refers to a rock or ore containing phosphate ions. Inorganic phosphates are mined to obtain phosphorus for use in agriculture and industry.

The largest global producer and exporter of phosphates is Morocco. Within North America, the largest deposits lie in the Bone Valley region of central Florida, the Soda Springs region of southeastern Idaho, and the coast of North Carolina. Smaller deposits are located in Montana, Tennessee, Georgia, and South Carolina. The small island nation of Nauru and its neighbor Banaba Island, which used to have massive phosphate deposits of the best quality, have been mined excessively. Rock phosphate can also be found in Egypt, Israel, Western Sahara, Navassa Island, Tunisia, Togo, and Jordan, countries that have large phosphate-mining industries.

Phosphorite mines are primarily found in:

• North America: Main article: Phosphate mining in the United States United States, especially Florida, with lesser deposits in North Carolina, Idaho, and Tennessee
• Africa: Morocco, Algeria, Egypt, Western Sahara, Niger, Senegal, Togo, Tunisia.
• Middle East: Israel, Saudi Arabia, Jordan, Syria, Iran and Iraq, at the town of Akashat, near the Jordanian border.
• Central Asia: Kazakhstan
• Oceania: Australia, Makatea, Nauru, and Banaba Island

In 2007, at the current rate of consumption, the supply of phosphorus was estimated to run out in 345 years. However, some scientists thought that a "peak phosphorus" will occur in 30 years and Dana Cordell from Institute for Sustainable Futures said that at "current rates, reserves will be depleted in the next 50 to 100 years". Reserves refer to the amount assumed recoverable at current market prices, and, in 2012, the USGS estimated 71 billion tons of world reserves, while 0.19 billion tons were mined globally in 2011. Phosphorus comprises 0.1% by mass of the average rock (while, for perspective, its typical concentration in vegetation is 0.03% to 0.2%), and consequently there are quadrillions of tons of phosphorus in Earth's 3 * 10 ton crust, albeit at predominantly lower concentration than the deposits counted as reserves from being inventoried and cheaper to extract; if it is assumed that the phosphate minerals in phosphate rock are hydroxyapatite and fluoroapatite, phosphate minerals contain roughly 18.5% phosphorus by weight and if phosphate rock contains around 20% of these minerals, the average phosphate rock has roughly 3.7% phosphorus by weight.

Some phosphate rock deposits, such as Mulberry in Florida, are notable for their inclusion of significant quantities of radioactive uranium isotopes. This syndrome is noteworthy because radioactivity can be released into surface waters in the process of application of the resultant phosphate fertilizer (e.g. in many tobacco farming operations in the southeast US).

In December 2012, Cominco Resources announced an updated JORC compliant resource of their Hinda project in Congo-Brazzaville of 531 Mt, making it the largest measured and indicated phosphate deposit in the world.

Production

The three principal phosphate producer countries (China, Morocco and the United States) account for about 70% of world production.

Production and global reserves of natural phosphate by country in 2015
(USGS, 2016)

Country	Production (millions kg)	Share of global production (%)	Reserves (millions kg)
Algeria	1,200	0.54	2,200,000
Australia	2,600	1.17	1,030,000
Brazil	6,700	3.00	315,000
China	100,000	44.83	3,700,000
Egypt	5,500	2.47	1,250,000
India	1,100	0.49	65,000
Iraq	200	0.09	430,000
Israel	3,300	1.48	130,000
Jordan	7,500	3.36	1,300,000
Kazakhstan	1,600	0.72	260,000
Mexico	1,700	0.76	30,000
Morocco	30,000	13.45	50,000,000
Peru	4,000	1.79	820,000
Russia	12,500	5.60	1,300,000
Saudi Arabia	3,300	1.48	956,000
Senegal	1,000	0.45	50,000
South Africa	2,200	0.99	1,500,000
Syria	750	0.34	1,800,000
Togo	1,000	0.45	30,000
Tunisia	4,000	1.79	100,000
United States	27,600	12.37	1,100,000
Vietnam	2,700	1.21	30,000
Other countries	2,600	1.17	380,000
Total	223,000	100	69,000,000

Ecology

In ecological terms, because of its important role in biological systems, phosphate is a highly sought after resource. Once used, it is often a limiting nutrient in environments, and its availability may govern the rate of growth of organisms. This is generally true of freshwater environments, whereas nitrogen is more often the limiting nutrient in marine (seawater) environments. Addition of high levels of phosphate to environments and to micro-environments in which it is typically rare can have significant ecological consequences. For example, blooms in the populations of some organisms at the expense of others, and the collapse of populations deprived of resources such as oxygen (see eutrophication) can occur. In the context of pollution, phosphates are one component of total dissolved solids, a major indicator of water quality, but not all phosphorus is in a molecular form that algae can break down and consume.

Calcium hydroxyapatite and calcite precipitates can be found around bacteria in alluvial topsoil. As clay minerals promote biomineralization, the presence of bacteria and clay minerals resulted in calcium hydroxyapatite and calcite precipitates.

Phosphate deposits can contain significant amounts of naturally occurring heavy metals. Mining operations processing phosphate rock can leave tailings piles containing elevated levels of cadmium, lead, nickel, copper, chromium, and uranium. Unless carefully managed, these waste products can leach heavy metals into groundwater or nearby estuaries. Uptake of these substances by plants and marine life can lead to concentration of toxic heavy metals in food products.

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See also

• Pyrophosphate – (P
  ₂O
  ₇)
  
• Polyphosphate – FORMULA NEEDS EDITING/FORMATTING: (HP
  _nO
  ₃)
  _(n+1)
• Metaphosphate – FORMULA NEEDS EDITING/FORMATTING: (P
  _nO
  _3n)
  _(n)
• Fertilizer
• Hypophosphite – H
  ₂(PO
  ₂)
  
• Organophosphorus compounds
• Phosphate – OP(OR)₃, such as triphenyl phosphate
• Phosphate conversion coating
• Phosphate soda, a soda fountain beverage
• Phosphinate – OP(OR)R₂
• Phosphine – PR₃
• Phosphine oxide – OPR₃
• Phosphinite – P(OR)R₂
• Phosphite – P(OR)₃
• Phosphogypsum
• Phosphonate – OP(OR)₂R
• Phosphonite – P(OR)₂R
• Phosphorylation
• Diammonium phosphate - (NH₄)₂HPO₄
• Disodium phosphate – Na₂HPO₄
• Monosodium phosphate – NaH₂PO₄
• Sodium tripolyphosphate – Na₅P₃O₁₀
• Ouled Abdoun Basin

References

1. "Phosphates – PubChem Public Chemical Database". The PubChem Project. USA: National Center of Biotechnology Information.
2. ^ "Phosphate Primer". Florida Industrial and Phosphate Research Institute. Florida Polytechnic University. Archived from the original on 29 August 2017. {{cite web}}: Unknown parameter |deadurl= ignored (|url-status= suggested) (help)
3. Campbell, Neil A.; Reece, Jane B. (2005). Biology (Seventh ed.). San Francisco, California: Benjamin Cummings. p. 65. ISBN 0-8053-7171-0.
4. Reilly, Michael (May 26, 2007). "How Long Will it Last?". New Scientist. 194 (2605): 38–9. Bibcode:2007NewSc.194...38R. doi:10.1016/S0262-4079(07)61508-5.
5. Leo Lewis (2008-06-23). "Scientists warn of lack of vital phosphorus as biofuels raise demand". The Times.
6. U.S. Geological Survey Phosphate Rock
7. U.S. Geological Survey Phosphorus Soil Samples
8. Floor Anthoni. "Abundance of Elements". Seafriends.org.nz. Retrieved 2013-01-10.
9. American Geophysical Union, Fall Meeting 2007, abstract #V33A-1161. Mass and Composition of the Continental Crust
10. Central Florida Phosphate Industry: Environmental Impact Statement. Vol. 2. United States. Environmental Protection Agency. 1979.
11. C. Michael Hogan (2010). Mark McGinley and C. Cleveland (Washington, DC.: National Council for Science and the Environment) (ed.). "Water pollution". Encyclopedia of Earth. Archived from the original on 2010-09-16.
12. "Updated Hinda Resource Announcement: Now world's largest phosphate deposit (04/12/2012)". Cominco Resources.
13. USGS Minerals Year Book - Phosphate Rock
14. Hochanadel, Dave (December 10, 2010). "Limited amount of total phosphorus actually feeds algae, study finds". Lake Scientist. Retrieved June 10, 2012. ioavailable phosphorus – phosphorus that can be utilized by plants and bacteria – is only a fraction of the total, according to Michael Brett, a UW engineering professor ...
15. ^ Schmittner KE, Giresse P (1999). "Micro-environmental controls on biomineralization: superficial processes of apatite and calcite precipitation in Quaternary soils, Roussillon, France". Sedimentology. 46 (3): 463–76. Bibcode:1999Sedim..46..463S. doi:10.1046/j.1365-3091.1999.00224.x.
16. Gnandi, K.; Tchangbedjil, G.; Killil, K.; Babal, G.; Abbel, E. (March 2006). "The Impact of Phosphate Mine Tailings on the Bioaccumulation of Heavy Metals in Marine Fish and Crustaceans from the Coastal Zone of Togo". Mine Water and the Environment. 25 (1): 56–62. doi:10.1007/s10230-006-0108-4.

External links

• US Minerals Databrowser provides data graphics covering consumption, production, imports, exports and price for phosphate and 86 other minerals
• Phosphate: analyte monograph – The Association for Clinical Biochemistry and Laboratory Medicine

v t e Phosphate minerals
Crystalline	Allanpringite Beraunite Brazilianite Eosphorite Fluorapatite Hydroxyapatite Lithiophilite Metatorbernite Monazite Struvite Taranakite Variscite Wavellite Xenotime Wycheproofite
Cryptocrystalline	Turquoise Whitlockite
Amorphous	Santabarbaraite Scorodite
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