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Osmotic concentration, formerly known as osmolarity, [1] is the measure of solute concentration, defined as the number of osmoles (Osm) of solute per litre (L) of solution (osmol/L or Osm/L). The osmolarity of a solution is usually expressed as Osm/L (pronounced "osmolar"), in the same way that the molarity of a solution is expressed as "M ...
The formula used to solve for the increase in pressure at the point being considered is 〖∆σ〗_z = (IV)qM, where IV = influence value, q = pressure on the loaded area, and M = number of elements enclosed by loaded area.
Thereby soil bulk density is always less than soil particle density and is a good indicator of soil compaction. [47] The soil bulk density of cultivated loam is about 1.1 to 1.4 g/cm 3 (for comparison water is 1.0 g/cm 3). [48] Contrary to particle density, soil bulk density is highly variable for a given soil, with a strong causal relationship ...
The laboratory value measures the freezing point depression, properly called osmolality while the calculated value is given in units of osmolarity. Even though these values are presented in different units, when there is a small amount of solute compared to total volume of solution, the absolute values of osmolality vs. osmolarity are very close.
This formula applies when the solute concentration is sufficiently low that the solution can be treated as an ideal solution. The proportionality to concentration means that osmotic pressure is a colligative property .
The Richards equation represents the movement of water in unsaturated soils, and is attributed to Lorenzo A. Richards who published the equation in 1931. [1] It is a quasilinear partial differential equation; its analytical solution is often limited to specific initial and boundary conditions. [2]
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The first modern theoretical models for soil consolidation were proposed in the 1920s by Terzaghi and Fillunger, according to two substantially different approaches. [1] The former was based on diffusion equations in eulerian notation, whereas the latter considered the local Newton’s law for both liquid and solid phases, in which main variables, such as partial pressure, porosity, local ...