enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Lime sulfur - Wikipedia

    en.wikipedia.org/wiki/Lime_sulfur

    Lime sulfur reacts with strong acids (including stomach acid) to produce highly toxic hydrogen sulfide (rotten egg gas) and indeed usually has a distinct "rotten egg" odor to it. Lime sulfur is not flammable but can release highly irritating sulfur dioxide gas when in a fire. Safety goggles and impervious gloves must be worn while handling lime ...

  3. Sulfide - Wikipedia

    en.wikipedia.org/wiki/Sulfide

    Sulfide (also sulphide in British English) [2] is an inorganic anion of sulfur with the chemical formula S 2− or a compound containing one or more S 2− ions. Solutions of sulfide salts are corrosive. Sulfide also refers to large families of inorganic and organic compounds, e.g. lead sulfide and dimethyl sulfide.

  4. Catalyst poisoning - Wikipedia

    en.wikipedia.org/wiki/Catalyst_poisoning

    Poisoning often involves compounds that chemically bond to a catalyst's active sites. Poisoning decreases the number of active sites, and the average distance that a reactant molecule must diffuse through the pore structure before undergoing reaction increases as a result. [4] As a result, poisoned sites can no longer alter the rate of reaction ...

  5. Phosphorus sulfides - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_sulfides

    Phosphorus sulfides comprise a family of inorganic compounds containing only phosphorus and sulfur.These compounds have the formula P 4 S n with n ≤ 10. Two are of commercial significance, phosphorus pentasulfide (P 4 S 10), which is made on a kiloton scale for the production of other organosulfur compounds, and phosphorus sesquisulfide (P 4 S 3), used in the production of "strike anywhere ...

  6. Organosulfur chemistry - Wikipedia

    en.wikipedia.org/wiki/Organosulfur_chemistry

    Organosulfur chemistry is the study of the properties and synthesis of organosulfur compounds, which are organic compounds that contain sulfur. [1] They are often associated with foul odors, but many of the sweetest compounds known are organosulfur derivatives, e.g., saccharin.

  7. Organic sulfide - Wikipedia

    en.wikipedia.org/wiki/Organic_sulfide

    The nonbonding electrons on sulfur are delocalized into the π-system. As a consequence, thiophene exhibits few properties expected for a sulfide – thiophene is non-nucleophilic at sulfur and, in fact, is sweet-smelling. Upon hydrogenation, thiophene gives tetrahydrothiophene, C 4 H 8 S, which indeed does behave as a typical sulfide.

  8. Liver of sulfur - Wikipedia

    en.wikipedia.org/wiki/Liver_of_sulfur

    Oxidizing silver with liver of sulfur solution. Liver of sulfur is a loosely defined mixture of potassium sulfide, potassium polysulfide, potassium thiosulfate, and likely potassium bisulfide. Synonyms include hepar sulfuris, sulfur, sulfurated potash and sulfurated potassa. There are two distinct varieties: "potassic liver of sulfur" and ...

  9. Sodium polysulfide - Wikipedia

    en.wikipedia.org/wiki/Sodium_polysulfide

    Sodium polysulfide can be produced by dissolving sulfur in a solution of sodium sulfide. [4] Alternatively they are produced by the redox reaction of aqueous sodium hydroxide with sulfur at elevated temperatures. [5] Finally they arise by the reduction of elemental sulfur with sodium, a reaction often conducted in anhydrous ammonia.