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The red line on the predominance diagram is not quite horizontal due to the simultaneous equilibrium with the chromate ion. The hydrogen chromate ion may be protonated, with the formation of molecular chromic acid, H 2 CrO 4, but the pK a for the equilibrium H 2 CrO 4 ⇌ HCrO − 4 + H + is not well characterized. Reported values vary between ...
The Pourbaix diagram for chromium in pure water, perchloric acid, or sodium hydroxide [1] [2]. Chromium compounds are compounds containing the element chromium (Cr). Chromium is a member of group 6 of the transition metals.
Loss of the second proton occurs in the pH range 4–8, making the ion [HCrO 4] − a weak acid. [citation needed] Molecular chromic acid could in principle be made by adding chromium trioxide to water (cf. manufacture of sulfuric acid). CrO 3 + H 2 O ⇌ H 2 CrO 4. In practice, the reverse reaction occurs: molecular chromic acid dehydrates ...
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3 has the corundum structure, consisting of a hexagonal close packed array of oxide anions with 2 ⁄ 3 of the octahedral holes occupied by chromium. Similar to corundum, Cr 2 O 3 is a hard, brittle material (Mohs hardness 8 to 8.5). [3] It is antiferromagnetic up to 307 K, the Néel temperature.
Chromate and dichromate have equal concentrations. Setting [CrO 2− 4] equal to [Cr 2 O 2− 7] in Eq. 3 gives [CrO 2− 4] = 1 / β 2 [H +] 2 . The predominance diagram is interpreted as follows. The chromate ion is the predominant species in the region to the right of the green and blue lines. Above pH ~6.75 it is always the ...
Chromium(VI) oxide peroxide is the name given to a collection of chromium coordination complexes. They have the formula CrO(O 2) 2 L where L is a ligand. These species are dark blue and often labile. They all feature oxo ligand and two peroxo ligands, with the remaining coordination sites occupied by water, hydroxide, ether, or other Lewis ...
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