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  2. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    Esterifications of phosphoric acid with alcohols proceed less readily than the more common carboxylic acid esterifications, with the reactions rarely proceeding much further than the phosphate mono-ester. The reaction requires high temperatures, under which the phosphoric acid can dehydrate to form poly-phosphoric acids.

  3. Sodium hexametaphosphate - Wikipedia

    en.wikipedia.org/wiki/Sodium_hexametaphosphate

    Sodium hexametaphosphate is the alkali salt of one of the series of polymetaphosphoric acids (acids formed by the polymerization of phosphate groups). [14] Hexametaphosphoric acid was first made in 1825 by the German chemist Johann Frederich Philipp Engelhart (1797-1853). [ 15 ]

  4. Trixylyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trixylyl_phosphate

    Trixylyl phosphate (TXP) is an aromatic phosphate ester. It was historically used as a flame retardant for acetate plastics (cellulose nitrate and cellulose acetate) and PVC. It also saw significant use as a fire-resistant hydraulic fluid. Trixylyl phosphate is now banned or restricted in several jurisdictions, due to its poor safety profile.

  5. Skydrol - Wikipedia

    en.wikipedia.org/wiki/Skydrol

    Skydrol is a brand name of fire-resistant hydraulic fluid [1] used in aviation and aerospace applications. It is a phosphate ester-based fluid that is known for its excellent fire resistance and ability to withstand extreme temperature and pressure conditions.

  6. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/.../Phosphoric_acids_and_phosphates

    Likewise, tripolyphosphoric acid H 5 P 3 O 10 yields at least five anions [H 5−k P 3 O 10] k−, where k ranges from 1 to 5, including tripolyphosphate [P 3 O 10] 5−. Tetrapolyphosphoric acid H 6 P 4 O 13 yields at least six anions, including tetrapolyphosphate [P 4 O 13] 6−, and so on. Note that each extra phosphoric unit adds one extra ...

  7. Diethyl phosphorochloridate - Wikipedia

    en.wikipedia.org/wiki/Diethyl_phosphorochloridate

    As a reagent in organic synthesis, it is used to convert alcohols to the corresponding diethylphosphate esters. It is a colorless liquid with a fruity odor. It is a corrosive, and as a cholinesterase inhibitor, highly toxic through dermal absorption. [1] The molecule is tetrahedral.

  8. Di(2-ethylhexyl)phosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Di(2-ethylhexyl)phosphoric...

    Compared to phosphate extractants, amines are more selective for uranium, extract the uranium faster, and are easily stripped with a wider variety of reagents. However, the phosphates are more tolerant of solids in the feed solution and show faster phase separation.

  9. Phosphate ester - Wikipedia

    en.wikipedia.org/?title=Phosphate_ester&redirect=no

    This page was last edited on 12 April 2006, at 22:24 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...