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  2. Polystyrene sulfonate - Wikipedia

    en.wikipedia.org/wiki/Polystyrene_sulfonate

    Water softening is achieved by percolating hard water through a bed of the sodium form of cross-linked polystyrene sulfonate. The hard ions such as calcium (Ca 2+) and magnesium (Mg 2+) adhere to the sulfonate groups, displacing sodium ions. The resulting solution of sodium ions is softened.

  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. Water softening - Wikipedia

    en.wikipedia.org/wiki/Water_softening

    Brine draw: Water is directed through a jet pump, which pulls salt water from the brine tank, before the water and brine pass through the resin bed in the normal direction, if co-current, or in the reverse direction, if counter-current. [11] The output of this typically thirty-minute process is discarded through the drain hose.

  5. Sulfonate - Wikipedia

    en.wikipedia.org/wiki/Sulfonate

    The sulfonate ion. In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.

  6. α-Olefin sulfonate - Wikipedia

    en.wikipedia.org/wiki/Α-Olefin_Sulfonate

    α-Olefin sulfonates with linear alkenyl radicals from C 12 to C 18 are used as anionic surfactants in various areas of application due to their pronounced foam formation [clarification needed] and foam stability (even with high water hardness), excellent fat-dissolving power and oil dissolving power as well as a favorable ecological profile and low aquatic toxicity and human toxicity.

  7. Sodium benzenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_benzenesulfonate

    The compound typically crystallizes from water as the monohydrate. [ 1 ] Heating this salt in strong base results in desulfonation , giving, after acid workup , phenol [ 2 ] This reaction was at one time, the principal route to phenol.

  8. TPPTS - Wikipedia

    en.wikipedia.org/wiki/Tppts

    3,3′,3′′-Phosphanetriyltris(benzenesulfonic acid) trisodium salt (abbreviated TPPTS), is an organic compound that is also known as sodium triphenylphosphine trisulfonate. The compound has the formula P(C 6 H 4 SO 3 Na) 3. This white solid is an unusual example of a water-soluble phosphine. Its complexes are also water-soluble. [2]

  9. Sodium p-toluenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_p-toluenesulfonate

    It is white, water-soluble solid. It is produced by the neutralization toluenesulfonic acid with sodium hydroxide. It is also a common product from the reactions of sodium-based reagents with toluenesulfonates. [1] Heating this salt in strong base results in desulfonation, giving, after acid workup, p-cresol. [2]

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