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  2. Chromium trioxide - Wikipedia

    en.wikipedia.org/wiki/Chromium_trioxide

    It is the acidic anhydride of chromic acid, and is sometimes marketed under the same name. [6] This compound is a dark-purple solid under anhydrous conditions and bright orange when wet. The substance dissolves in water accompanied by hydrolysis. [clarification needed] Millions of kilograms are produced annually, mainly for electroplating. [7]

  3. Chromium(III) oxide - Wikipedia

    en.wikipedia.org/wiki/Chromium(III)_oxide

    Because of its considerable stability, chromia is a commonly used pigment. It was originally called viridian. It is used in paints, inks, and glasses. It is the colorant in "chrome green" and "institutional green." Chromium(III) oxide is a precursor to the magnetic pigment chromium dioxide, by the following reaction: [7] Cr 2 O 3 + 3 CrO 3 → ...

  4. Chromic acid - Wikipedia

    en.wikipedia.org/wiki/Chromic_acid

    This kind of chromic acid may be used as a cleaning mixture for glass. Chromic acid may also refer to the molecular species, H 2 CrO 4 of which the trioxide is the anhydride. Chromic acid features chromium in an oxidation state of +6 (and a valence of VI or 6). It is a strong and corrosive oxidizing agent and a moderate carcinogen.

  5. Chromium compounds - Wikipedia

    en.wikipedia.org/wiki/Chromium_compounds

    At yet lower pH values, further condensation to more complex oxyanions of chromium is possible. Both the chromate and dichromate anions are strong oxidizing reagents at low pH: [6] Cr 2 O 2− 7 + 14 H 3 O + + 6 e − → 2 Cr 3+ + 21 H 2 O (ε 0 = 1.33 V) They are, however, only moderately oxidizing at high pH: [6] CrO 2− 4 + 4 H 2 O + 3 e ...

  6. Chromate and dichromate - Wikipedia

    en.wikipedia.org/wiki/Chromate_and_dichromate

    Further condensation reactions can occur in strongly acidic solution with the formation of trichromates, Cr 3 O 2− 10, and tetrachromates, Cr 4 O 2− 13. [2] All polyoxyanions of chromium(VI) have structures made up of tetrahedral CrO 4 units sharing corners. [3] The hydrogen chromate ion, HCrO 4 −, is a weak acid: HCrO − 4 ⇌ CrO 2−

  7. Talk:Chromic acid - Wikipedia

    en.wikipedia.org/wiki/Talk:Chromic_acid

    CrO3 dissolves in water to make a solution containing H+ and CrO4-- ions, which is a dilute solution of chromic acid. Interestingly, CrO3 shows acid properties without water being present e.g. CaO + CrO3 --> CaCrO4. It is an example of a "Lewis acid" which meets the (broader) definition of an acid suggested by the chemist G.N.Lewis in the 1920s.

  8. Chromium(VI) oxide peroxide - Wikipedia

    en.wikipedia.org/wiki/Chromium(VI)_oxide_peroxide

    Structure of CrO(O 2) 2 (pyridine).Hydrogen atoms bonded to carbon atoms are omitted. Color code: Cr = gray, C= black, H = white, O= red, N = blue. Chromium(VI) oxide peroxide is formed by the addition of acidified hydrogen peroxide solutions to solutions of metal chromates or dichromates, such as sodium chromate or potassium dichromate.

  9. Chromium(II) oxide - Wikipedia

    en.wikipedia.org/wiki/Chromium(II)_oxide

    It is readily oxidized by the atmosphere. CrO is basic, while CrO 3 is acidic, and Cr 2 O 3 is amphoteric. [3] CrO occurs in the spectra of luminous red novae, which occur when two stars collide. It is not known why red novae are the only objects that feature this molecule; one possible explanation is an as-yet-unknown nucleosynthesis process. [4]