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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 about −0.8 and 1.6. [4] The dichromate ion is a somewhat weaker base than the chromate ion: [5]
Potassium chromate is the inorganic compound with the formula K 2 CrO 4. This yellow solid is the potassium salt of the chromate anion. It is a common laboratory chemical, whereas sodium chromate is important industrially.
The mineral chromite is an iron chromium oxide with empirical formula FeCr 2 O 4. Structurally, it belongs to the spinel group. Magnesium can substitute for iron in variable amounts as it forms a solid solution with magnesiochromite (MgCr 2 O 4);. [1] Zincochromite is another example.
The structure of nickel chromate is the same as for chromium vanadate, CrVO 4. Crystals have an orthorhombic structure with unit cell sizes a = 5.482 Å, b = 8.237 Å, c = 6.147 Å. The cell volume is 277.6 Å 3 with four formula per unit cell. [5] [7] Nickel chromate is dark in colour, unlike most other chromates which are yellow. [3]
Sodium chromate is the inorganic compound with the formula Na 2 CrO 4. It exists as a yellow hygroscopic solid, which can form tetra-, hexa-, and deca hydrates . It is an intermediate in the extraction of chromium from its ores.
Partial predominance diagram for chromate. Molecular chromic acid, H 2 CrO 4, in principle, resembles sulfuric acid, H 2 SO 4. It would ionize accordingly: H 2 CrO 4 ⇌ [HCrO 4] − + H + The pK a for the equilibrium is not well characterized. Reported values vary between about −0.8 to 1.6. [4]
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Lead(II) chromate can be produced by treating sodium chromate with lead salts such as lead(II) nitrate or by combining lead(II) oxide with chromic acid.. Related lead sulfochromate pigments are produced by the replacement of some chromate by sulfate, resulting in a mixed lead-chromate-sulfate compositions Pb(CrO 4) 1−x (SO 4) x.