Difference between revisions of "Silver chlorate"

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===Relevant Sciencemadness threads===
 
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*[http://www.sciencemadness.org/talk/viewthread.php?tid=83524 Silver chlorate-properties]
 
*[http://www.sciencemadness.org/talk/viewthread.php?tid=83524 Silver chlorate-properties]
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*[http://www.sciencemadness.org/talk/viewthread.php?tid=155770 Chlorate using silver oxide?]
  
 
[[Category:Chemical compounds]]
 
[[Category:Chemical compounds]]

Latest revision as of 16:07, 12 August 2023

Silver chlorate
Names
IUPAC name
Silver(I) chlorate
Other names
Argentous chlorate
Silver(I) chlorate(V)
Properties
AgClO3
Molar mass 191.319 g/mol
Appearance White colorless solid
Odor Odorless
Density 4.443 g/cm3 (20 °C)
Melting point 230–231 °C (446–448 °F; 503–504 K) (decomposes)
Boiling point 270 °C (518 °F; 543 K) (decomposes)
8.52 g/100 ml (5 °C)
10 g/100 ml (15 °C)
18.03 g/100 ml (25 °C)
23.74 g/100 ml (35 °C)
50 g/100 ml (80 °C)[1][2]
Solubility Reacts with acids and bases
Sparingly soluble in alcohols
Vapor pressure ~0 mmHg
Thermochemistry
141,838 J·mol-1·K-1
-30,292 kJ/mol
Hazards
Safety data sheet Sigma-Aldrich
Flash point Non-flammable
Related compounds
Related compounds
Silver perchlorate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Silver chlorate is an inorganic compound with the formula AgClO3.

Properties

Chemical

Silver chlorate decomposes upon gentle heating to release oxygen.

AgClO3 → AgCl + 3/2 O2

It is a powerful oxidizer, and mixtures with organic compounds, like sugars, will burn vigorously.[4]

Silver chlorate can be used to prepare other chlorate salts, via double displacement with a metal chloride.

MCl + AgClO3 → MClO3 + AgCl ↓

Silver chlorate has been proven to be an effective oxidizing agent for some organic compounds, like crotonic acid and isocrotonic acid, which are oxidized to dZ-threo-a,P-dihydroxybutyric acid and to dl-erythro-a,P-dihydroxybutyric acid, respectively.[5]

Physical

Silver chlorate is a colorless crystalline solid, soluble in water.

Explosive

Pure silver chlorate is stable in dry and moist air. After being stored for a few days the compound becomes very sensitive and explodes on touch. On exposure to daylight, AgClO3 slowly decomposes and becomes dark and turns into an extremely explosive compound. This can also happen on the stoppers of bottles and may lead to detonation when the stopper is removed. AgClO3 decomposes to AgCl with low heat or on melting, but when quickly heated it explodes or deflagrates.[6]

Availability

Silver chlorate is difficult to find, but many chemical suppliers will often have it in their stock, at high price.

Preparation

The most common route for preparing silver chlorate, involves the double displacement reaction of silver nitrate with sodium chlorate, which yields both silver chlorate and sodium nitrate. Fractional recrystallization is used to separate the two compounds from the solution.[7][8]

AgNO3 + NaClO3 → AgClO3 + NaNO3

The most convenient synthesis route involves the double displacement reaction between barium chlorate and silver(I) fluoride. Since barium fluoride is almost insoluble in water, the resulting silver chlorate obtained this way is very pure. Main disadvantage is that silver fluoride is expensive to make.

Ba(ClO3)2 + 2 AgF → 2 AgClO3 + BaF2

Another direct route involves the careful addition of chloric acid to silver oxide or silver carbonate.[9][10]

2 HClO3 + Ag2O → 2 AgClO3 + H2O
2 HClO3 + Ag2CO3 → 2 AgClO3 + H2O + CO2

Reaction with silver metal will also produce silver chlorate, but silver chloride is also produced as side product.[11][12]

6 HClO3 + 6 Ag → 5 AgClO3 + AgCl + 3 H2O

While simpler than the first route, one major issue in using HClO3 is that it is unstable at high concentrations, meaning the resulting product will be dilute, and possibly contaminated with silver perchlorate, from perchloric acid, which results from the rapid decomposition of conc. chloric acid.

There are other more accessible routes:

Bubbling chlorine gas through an aqueous suspension of silver oxide, similar to the preparation of alkali chlorates has been described as another synthesis route.[13][14]

Ag2O + Cl2 + H2O → AgClO3 + AgCl ↓

This works because it produces hypochlorous acid/silver hypochlorite, which rapidly breaks down into chlorate and chloride. However, the resulting AgCl will lower the yield of this route, and filtration is required to remove it from the solution.[15]

Projects

  • Make other chlorates
  • Primary explosive

Handling

Safety

Silver chlorate is harmful, due to its chlorate anion. It is also a sensitive explosive and must not be kept for long periods of time, as if it builds up on the bottle cap, it may detonate when one opens the bottle.

Storage

Silver chlorate should not be kept for long periods of time and must be used quickly. Ampouling may be used, but the compound must not be exposed to light.

Disposal

Addition of an aq. solution of NaOH will cause the silver to precipitate as silver oxide, while the chlorate remains in the solution. The silver should be recycled, while the chlorate can be reduced to chloride using a reducing agent.

References

  1. Справочник химика. - Т. 3. - М.-Л.: Химия, 1965 (Handbook of a chemist. - T. 3. - M.-L.: Chemistry, 1965)
  2. Ефимов А.И. и др. Свойства неорганических соединений. Справочник. - Л.: Химия, 1983 (Efimov A.I. etc. Properties of inorganic compounds. Directory. - L .: Chemistry, 1983)
  3. Barin I. Thermochemical Data of Pure Substances. - VCH, 1995 pp. 7
  4. Silver Chlorate(AgClO3) Test
  5. Inorganic Syntheses, Silver Chlorate, D. G. Nicholson, Cearles E. Holley Jr., George W. Watt, Joe C. Evans
  6. Gmelins Handbuch der Anorganischen Chemie, Silber Teil B1, Verlag Chemie GmbH, Weinheim/Bergstraße, 8th edition 1971, p. 503
  7. Inorganic Syntheses, Silver Chlorate, D. G. Nicholson, Cearles E. Holley Jr., George W. Watt, Joe C. Evans
  8. How to Make Silver Chlorate (Good Prep for Beginners)
  9. Hendrixson; Journal of the American Chemical Society; vol. 25; (1903); p. 639
  10. Foote, H. W.; Saxton, B.; Journal of the American Chemical Society; vol. 36; (1914); p. 1704 - 1708
  11. https://scholarworks.uni.edu/cgi/viewcontent.cgi?article=7036&context=pias
  12. Hendrixson; Journal of the American Chemical Society; vol. 25; (1903); p. 639
  13. Pierron, P.; Bulletin de la Societe Chimique de France; vol. 8; (1941); p. 664 - 670
  14. Gmelin Handbuch der Anorganischen Chemie; vol. Cl: SVol.B2; 3, page 320 - 322
  15. Balard; Annales de Chimie et de Physique; vol. 57; (1834); p. 241 - 241

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