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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]
Chromate conversion coating or alodine coating is a type of conversion coating used to passivate steel, aluminium, zinc, cadmium, copper, silver, titanium, magnesium, and tin alloys. [ 1 ] : p.1265 [ 2 ] The coating serves as a corrosion inhibitor , as a primer to improve the adherence of paints and adhesives , [ 2 ] as a decorative finish, or ...
pyridinium dichromate (PDC) is the pyridium salt of dichromate, [Cr 2 O 7] 2-. pyridinium chlorochromate (PCC) is the pyridinium salt of [CrO 3 Cl] −. These salts are less reactive, more easily handled, and more selective than Collins reagent in oxidations of alcohols.
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 ...
For lab and small scale preparations a mixture of chromite ore, sodium hydroxide and sodium nitrate reacting at lower temperatures may be used (even 350 C in the corresponding potassium chromate system). [2] Subsequent to its formation, the chromate salt is converted to sodium dichromate, the precursor to most chromium compounds and materials. [3]
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