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The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/(100 mL)), unless shown otherwise. The substances are listed in alphabetical order.
All data as presented in these tables is for materials in their standard state, which is at 25 °C and 100 kPa by definition. If values are given for other conditions, this is explicitly indicated. If values are given for other conditions, this is explicitly indicated.
The values in g/L and g/kg are similar for water, but that may not be the case for other solvents.) Alternatively, the solubility of a solute can be expressed in moles instead of mass. For example, if the quantity of solvent is given in kilograms , the value is the molality of the solution (mol/kg).
The values are sometimes approx. similar to the ones in the table, some other times, off quite a bit. I could do a major revamp of the whole table, and add the values with (as i think is best to remove obscurity) a reference tag at each value excerpt from CRC.
The adjacent table shows the result for [Ca 2+] and [H +] (in the form of pH) as a function of ambient partial pressure of CO 2 (K sp = 4.47 × 10 −9 has been taken for the calculation). At atmospheric levels of ambient CO 2 the table indicates that the solution will be slightly alkaline with a maximum CaCO 3 solubility of 47 mg/L.
A solubility equilibrium exists when a chemical compound in the solid state is in chemical equilibrium with a solution containing the compound. This type of equilibrium is an example of dynamic equilibrium in that some individual molecules migrate between the solid and solution phases such that the rates of dissolution and precipitation are equal to one another.
Iron(III) oxide in a vial. Iron(III) oxide or ferric oxide is the inorganic compound with the formula Fe 2 O 3.It occurs in nature as the mineral hematite, which serves as the primary source of iron for the steel industry.
Lead(II) fluoride can be prepared by treating lead(II) hydroxide or lead(II) carbonate with hydrofluoric acid: [3]. Pb(OH) 2 + 2 HF → PbF 2 + 2 H 2 O Alternatively, it is precipitated by adding hydrofluoric acid to a lead(II) salt solution, or by adding a fluoride salt to a lead salt, such as potassium fluoride to a lead(II) nitrate solution, [4]