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  2. 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.

  3. 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 ...

  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. 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.

  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. 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 ...

  8. Doctor sweetening process - Wikipedia

    en.wikipedia.org/wiki/Doctor_sweetening_process

    The described chemistry is also the basis of the doctor test for the sweetness or sourness of gasoline (i.e., the extent of sulfur contamination). A gasoline is described as doctor sweet if, after shaking with sodium plumbite solutions, the addition of powdered sulfur fails to produce a dark precipitate of lead sulfide.

  9. Iron (II,III) sulfide - Wikipedia

    en.wikipedia.org/wiki/Iron(II,III)_sulfide

    Iron(II,III) sulfide is a blue-black (sometimes pinkish [citation needed]) chemical compound of iron and sulfur with formula Fe 3 S 4 or FeS·Fe 2 S 3, which is much similar to iron(II,III) oxide. It occurs naturally as the sulfide mineral greigite and is magnetic. It is a bio-mineral produced by and found in magnetotactic bacteria.

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