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Two crystalline forms are known, both being very similar to the corresponding potassium sulfate. Orthorhombic β-K 2 CrO 4 is the common form, but it converts to an α-form above 66 °C. [1] These structures are complex, although the chromate ion adopts the typical tetrahedral geometry. [2]
When heated strongly, it decomposes with the evolution of oxygen. 4 K 2 Cr 2 O 7 → 4 K 2 CrO 4 + 2 Cr 2 O 3 + 3 O 2 When an alkali is added to an orange-red solution containing dichromate ions, a yellow solution is obtained due to the formation of chromate ions ( CrO 2− 4 ).
Predominance diagram for chromate. In aqueous solution, chromate and dichromate anions exist in a chemical equilibrium.. 2 CrO 2− 4 + 2 H + ⇌ Cr 2 O 2− 7 + H 2 O. The predominance diagram shows that the position of the equilibrium depends on both pH and the analytical concentration of chromium.
Table of specific heat capacities at 25 °C (298 K) unless otherwise noted. [citation needed] Notable minima and maxima are shown in maroon. Substance Phase Isobaric mass heat capacity c P J⋅g −1 ⋅K −1 Molar heat capacity, C P,m and C V,m J⋅mol −1 ⋅K −1 Isobaric volumetric heat capacity C P,v J⋅cm −3 ⋅K −1 Isochoric ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
It is obtained on a vast scale by roasting chromium ores in air in the presence of sodium carbonate: 2Cr 2 O 3 + 4 Na 2 CO 3 + 3 O 2 → 4 Na 2 CrO 4 + 4 CO 2. This process converts the chromium into a water-extractable form, leaving behind iron oxides.
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