Nernst’s division law states that a substance is divided between two solvents in a way that proportion of concentrations of that substance is at certain temperatures constant, under the condition that both solvents are in the same molecular state. Division coefficient is a proportion of substance concentration in solvents A i B at a defined temperature.
Appearance of division is used for substance extraction.
Vapour pressure is a colligative property of solutions. The vapour pressure of a solution is always lower than the vapour pressure of the pure solvent. Ratio of solution to pure solvent vapour pressures is approximately equal to the mole fraction of solvent in the solution.
Relative density (d) is the ratio of the density of a substance to the density of some reference substance. For liquids or solids it is the ratio of the density (usually at 20 °C) to the density of water at 4 °C. Since one must specify the temperature of both the sample and the water to have a precisely defined quantity, the use of this term is now discouraged. This quantity was formerly called specific gravity.
Relative molecular mass (Mr) is the ratio of the average mass per molecule or specified entity of a substance to 1/12 of the mass of nuclide 12C. Also called molecular weight. It is equal to the sum of the relative atomic masses of all the atoms that comprise a molecule. For example
Mr(H2SO4) = 2·Ar(H) + Ar(S) + 4·Ar(O)
= 2·1.0079 + 32.066 + 4·15.999
= 2.0158 + 32.066 + 63.996
= 98.078
Retardation factor, RF, (in planar chromatography) is a ratio of the distance travelled by the centre of the spot to the distance simultaneously travelled by the mobile phase:
The RF value is characteristic for any given compound on the same stationary phase using the same mobile phase for development of the plates. Hence, known RF values can be compared to those of unknown substances to aid in their identifications.
Salinity (S) is a measure of the quantity of dissolved salts in seawater. It is formally defined as the total amount of dissolved solids in seawater in parts per thousand (‰) by weight when all the carbonate has been converted to oxide, the bromide and iodide to chloride, and all organic matter is completely oxidized.
Chlorinity is the oldest of the salinity measures considered and is still a corner-stone in the study of dissolved material in seawater. Based on the principle of constant relative proportions it provides a measure of the total amount of dissolved material in seawater in terms of the concentration of halides. The relationship between chlorinity (Cl) and salinity as set forth in Knudsen’s tables is
In 1962, however, a better expression for the relationship between total dissolved salts and chlorinity was found to be
Practical Salinity (SP) was introduced as a replacement for Chlorinity. Practical Salinity is is relatively easy to measure using standard conductometers, measurements are more precise and less time consuming than measurements of Chlorinity and accurate measurements can even be made in situ. Practical salinity SP is defined on the Practical Salinity Scale of 1978 (PSS-78) in terms of the conductivity ratio K15 which is the electrical conductivity of the sample at temperature t68 = 15 °C and pressure equal to one standard atmosphere, divided by the conductivity of a standard potassium chloride (KCl) solution at the same temperature and pressure. The mass fraction of KCl in the standard solution is 0.0324356 (32.4356 g of KCl in 1 kg of solution).
Note that Practical Salinity is a unit-less quantity. Though sometimes convenient, it is technically incorrect to quote Practical Salinity in "psu". For most purposes one can assume that the psu and the ‰, are synonymous.
The global average salinity of ocean waters is about 35 ‰, that is, about 35 g of solid substances are dissolved in 1 kg of seawater.
Specific weight (γ) is defined as the ratio between the weight of a mass element, Δm, and the volume, ΔV, occupied by that element. As density (average) is defined as the ratio of a mass element and its volume, specific weight is equal to:
where g is gravitational acceleration.
Thermometers are devices for measuring temperature. Linear and volume thermal expansion are macroscopic properties of matter, which can be easily measured, relative to measurements of microscopic properties, on the basis of which, temperature is defined. Thermometers based on thermal expansion are secondary instruments that is, they have to be calibrated in comparison to a standard thermometer. In a thermometer with liquid, mercury or alcohol is placed in a small glass container. If temperature increases, the liquid undergoes volume expansion and rises in a capillary. The level of the raised liquid is the measure of temperature. Mercury thermometers measure temperatures in the temperature range between -39 °C and 300 °C. Alcohol thermometers measure lower temperatures. Bimetal thermometers have a spiral spring, which consists of two metals with different coefficients of linear expansion. When temperature changes, metals undergo different change in length and the consequence twisting of the spring is transferred to a pointer, the deflection of which is the measure of temperature.
Generalic, Eni. "Volumenski omjer." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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