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The strength of the bonds between the metal ion and water molecules in the primary solvation shell increases with the electrical charge, z, on the metal ion and decreases as its ionic radius, r, increases. Aqua ions are subject to hydrolysis. The logarithm of the first hydrolysis constant is proportional to z 2 /r for most aqua ions.
Copper(II) sulfate is an inorganic compound with the chemical formula Cu SO 4.It forms hydrates CuSO 4 ·nH 2 O, where n can range from 1 to 7. The pentahydrate (n = 5), a bright blue crystal, is the most commonly encountered hydrate of copper(II) sulfate, [10] while its anhydrous form is white. [11]
To ensure consistency and repeatability, the methods use in the chemical analysis of water samples are often agreed and published at a national or state level. By convention these are often referred to as "Blue book". [4] [5] Certain analyses are performed in-field (e.g. pH, specific conductance) while others involve sampling and laboratory ...
Electrical conductivity of water samples is used as an indicator of how salt-free, ion-free, or impurity-free the sample is; the purer the water, the lower the conductivity (the higher the resistivity). Conductivity measurements in water are often reported as specific conductance, relative to the conductivity of pure water at 25 °C.
As the titration progresses, the protons are neutralized to form water by the addition of NaOH. For each amount of NaOH added equivalent amount of hydrogen ions is removed. Effectively, the mobile H + cation is replaced by the less-mobile Na + ion, and the conductivity of the titrated solution as well as the measured conductance of the cell ...
This occurs because of the effect of solvation of water molecules: the smaller Li + binds most strongly to about four water molecules so that the moving cation species is effectively Li(H 2 O) + 4. The solvation is weaker for Na + and still weaker for K +. [4] The increase in halogen ion mobility from F − to Cl − to Br − is also due to ...