Schrödinger equation is the basic equation of wave mechanics which, for systems not dependent on time, takes the form:
where Ψ is the wavefunction, V is the potential energy expressed as a function of the spatial coordinates, E its total energy, 2 is the Laplacian operator, h is Planck’s constant, and m is the mass.
Seawater is a complex mixture of 96.5 % water, 3.5 % salts, and smaller amounts of other substances, including dissolved inorganic and organic materials, particulates, and a few atmospheric gases. The world's oceans cover nearly 71 % (361 840 000 km2) of the Earth's surface (510 100 000 km2), with an average depth of 3 682.2 m.
The density of seawater is higher than that of fresh water because of its higher salinity. Seawater's freezing point is lower than that of pure water and its boiling point is higher. The average salinity of the ocean is 35 ‰, which means that for every kilograms of water, there are 35 g of salt. The relative abundance of the major salts in seawater are constant regardless of the ocean. Only six elements and compounds comprise about 99 % of sea salts: chlorine (Cl-), sodium (Na+), sulfur (SO42-), magnesium (Mg2+), calcium (Ca2+), and potassium (K+).
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.
When a light ray comes on a boundary between two transparent media, it will be partly reflected and partly refracted. Both rays, reflected and refracted ray, lay in the plane of incidence. The angle of reflection is equal to the angle of incidence. The angle of refraction (Θ2) is related to the angle of incidence (Θ1) via Snell’s law:
where n1 and n2 are dimensionless constants - indexes of refraction of the two media.
Supercritical fluid chromatography (SFC) is a hybrid of gas and liquid chromatography. SFC is of importance because it permits the separation and determination of a group of compounds that are not conveniently handled by either gas or liquid chromatography. These compounds are either nonvolatile or thermally labile so that gas chromatography cannot be used and they do not contain functional groups that make possible detection by liquid chromatography. SFC has been applied to a wide variety of materials including natural prodcuts, drugs, foods, pesticides and herbicides, fossil fuels, explosives and propellants.
Tafel plot is the graph of the logarithm of the current density j against the overpotential η in electrochemistry in the high overpotential limit. An electrode when polarised frequently yields a current potential relationship over a region which can be approximated by:
where η is change in open circuit potential, i is the current density, B and i0 is constants. B is known as the Tafel Slope. If this behaviour is observed a plot of the semilogarithmic components is known as the Tafel line and the diagram is called the Tafel diagram.
Thermodynamic laws are the foundation of the science of thermodynamics:
First law: The internal energy of an isolated system is constant; if energy is supplied to the system in the form of heat dq and work dw, then the change in energy dU = dq + dw.
Second law: No process is possible in which the only result is the transfer of heat from a reservoir and its complete conversion to work.
Third law: The entropy of a perfect crystal approaches zero as the thermodynamic temperature approaches zero.
Triple point is the point in p,T space where the solid, liquid, and gas phases of a substance are in thermodynamic equilibrium.
Water ion product (Kw) is a concentration product of hydrogen and hydroxide ions. For the reaction:
the equilibrium expression would be:
Note that all pure liquid terms are omitted, hence H2O does not appear in the denominator. At 25 °C, Kw = 1.0×10-14 mol2dm-6 = (Ka)(Kb)
Work is the energy required to move an object against an opposing force. Work is usually expressed as a force times a displacement.
When a constant force F acts on a point-like object while the object moves through a displacement s, the force does work W on the object. If force and displacement are at a constant angle Θ to each other, the work is expressed by the scalar product of these two vectors:
When the force F on a point-like object is not constant that is, it depends on the position of the object, the work done by force while object moves from initial position with coordinates (xi, yi, zi) to final position with coordinates (xf, yf, zf)is given by expression:
Where Fx, Fy and Fz are scalar components of the force.
SI unit for work is joule (J); 1 J = 1 Nm = 1 kg m2 s-2. The electron-volt (eV) is commonly used in atomic and nuclear physics.
Generalic, Eni. "Univerzalna plinska konstanta." Croatian-English Chemistry Dictionary & Glossary. 29 June 2022. KTF-Split. {Date of access}. <https://glossary.periodni.com>.
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