Red phosphorus

Chemical compound From Wikipedia, the free encyclopedia

Red phosphorus is the common name of several forms of elemental phosphorus, often considered one of its allotropes. Its most common shape is an amorphous polymeric red solid that is stable in air.

Quick facts Identifiers, Properties ...
Red phosphorus
A sample of red phosphorus
Identifiers
3D model (JSmol)
DrugBank
EC Number
  • 231-768-7
UNII
UN number 1338
  • InChI=1S/P
  • Key: OAICVXFJPJFONN-UHFFFAOYSA-N
  • [P]
Properties
P
Molar mass 30.974 g·mol−1
Density 2.34 g/cm3
Melting point 590 °C (1,094 °F; 863 K)
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calciumSpecial hazards (white): no code
1
1
1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Amorphous red phosphorus is easily obtained when exposing white phosphorus to sunlight or heating, which was discovered in 1847 by Anton von Schrötter.[1] When sublimed in a vacuum, amorphous red phosphorus can transform into a crystalline form, known either as violet or Hittorf's phosphorus, after the name of its discoverer.[2] When this process is carried out in the presence of iodine, another crystalline is obtained alongside it, called fibrous red phosphorus.

Applications of amorphous red phosphorus include matches and fire retardants.

Amorphous red phosphorus

Amorphous red phosphorus chain fragments, with (top) or without (bottom) interchain connection[3][4]

Amorphous red phosphorus is polymeric in structure and therefore insoluble in most solvents. It is easily obtained by irradiation or heating of white phosphorus.[5]

The standard enthalpy of formation of amorphous red phosphorus is −17.6 kJ/mol.[4] it is the most kinetically stable form of phosphorus. Because of this, it does not exhibit the intense and comprehensive reactivity of white phosphorus.[2] and is much more stable under standard conditions. However, it is less stable than black phosphorus, the most thermodynamically stable allotrope of phosphorus.

Because of its polymeric structure, amorphous red phosphorus is insoluble in most solvents. It also shows semiconductor properties.[2]

Crystalline red phosphorus

Violet or Hittorf's phosphorus

Violet/Hitorff's phosphorus crystal structure

Hittorf's phosphorus, or violet phosphorus, is one of the crystalline forms of red phosphorus.[6][2]

Violet phosphorus can be prepared by sublimation of red phosphorus in a vacuum, in the presence of an iodine catalyst.[2]

It is chemically similar to red phosphorus. There are, however, subtle differences. Violet phosphorus ignites upon contact with air, while red phosphorus is impact stable. Violet phosphorus doesn't ignite in the presence of air upon room temperature contact with bromine, unlike red phosphorus.[citation needed] The reaction of red phosphorus and bromine alone does not generate a flame.[citation needed]

Fibrous red phosphorus

Fibrous red phosphorus crystal structure

Fibrous red phosphorus is another crystalline form of red phosphorus.[2] It is obtained along with violet phosphorus when red phosphorus is sublimed in a vacuum in the presence of iodine.[7]

It is structurally similar to violet phosphorus. However, in fibrous red phosphorus, phosphorus chains lie parallel instead of orthogonal, unlike violet phosphorus.[8][2]

Fibrous red phosphorus, similar to red phosphorus, displays activity as a photocatalyst.[7][9]

Applications

Flame retardants

Amorphous red phosphorus can be used as a very effective flame retardant, especially in thermoplastics (e.g. polyamide) and thermosets (e.g. epoxy resins or polyurethanes). The flame retarding effect is based on the formation of polyphosphoric acid. Together with the organic polymer material, these acids create a char which prevents flame propagation. The safety risks associated with phosphine generation and friction sensitivity of red phosphorus can be effectively minimized by stabilization and micro-encapsulation. For easier handling, red phosphorus is often used in form of dispersions or masterbatches in various carrier systems.[10]

However, for electronic/electrical systems, red phosphorus flame retardant has been effectively banned by major OEMs due to its tendency to induce premature failures.[11] One persistent problem is that red phosphorus in epoxy molding compounds induces elevated leakage current in semiconductor devices.[12] Another problem was acceleration of hydrolysis reactions in PBT insulating material.[13]

Safety matches

Red phosphorus is used, along with abrasives, on the strike pads of modern matches. Its discovery allowed for the development of safer matches (historically called safety matches), as well as much less hazardous manufacturing. The match head, containing potassium chlorate, will ignite upon friction with the strike pad.[14] However, the red color of the matchhead is due to addition of red iron oxide, and has nothing to do with phosphorus.[15]

Chemical synthesis

Amorphous Red phosphorus reacts with bromine and iodine to form phosphorus tribromide[16][17] and phosphorus triiodide. Both are useful as halogenating agents, for example in replacing the hydroxyl group of alcohols. Phosphorus triiodide can also be used to produce hydroiodic acid after hydrolysis. This reaction is notable in the illicit production of methamphetamine and Krokodil, where hydrogen iodide acts as a reducing agent.[18]

Red phosphorus is often used to prepare chemicals where the P-P bond is retained. Upon room temperature reaction with sodium chlorite, Na2H2P2O6 is formed.[19]

Red phosphorus can be used as an elemental photocatalyst for hydrogen formation from water.[20][2] It displays a steady hydrogen evolution rates of 633 μmol/(h⋅g) by the formation of small-sized fibrous phosphorus.[21] It has also been researched as a sodium ion battery anode.[22][3]

References

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