CHEMISTRY GLOSSARY

salinity    →   salinitet

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 (S_P) 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 S_P 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.

salt fog test    →   ispitivanje u slanoj komori

Salt fog test is an accelerated corrosion test in which specimens are exposed to a fine mist of a solution usually containing sodium chloride (typically 5 %). Other contaminants can be added according to desired conditions. It is mainly used to determine the effectiveness of material finishes and protective coatings on materials. Salt-fog testing is also used to determine the effects of salt deposits on the electrical functions of electronic assemblies.

seawater    →   more

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 (SO₄^2-), magnesium (Mg²⁺), calcium (Ca²⁺), and potassium (K⁺).

sodium    →   natrij

Sodium was discovered by Sir Humphry Davy (England) in 1807. The origin of the name comes from the Latin word natrium meaning sodium carbonate. It is soft silvery-white metal. Fresh surfaces oxidize rapidly. Reacts vigorously, even violently with water. Reacts with water to give off flammable gas. Burns in air with a brilliant white flame. Sodium is obtained by electrolysis of melted sodium chloride (salt), borax and cryolite. Metallic sodium is vital in the manufacture of organic compounds. Sodium chloride (NaCl) is table salt. Liquid sodium is used to cool nuclear reactors.

sol    →   sol

Sols are dispersions of small solid particles in a liquid. The particles may be macromolecules or may be clusters of small molecules. Lyophobic sols are those in which there is no affinity between the dispersed phase and the liquid (e.g. silver chloride dispersed in water). Lyophobic sols are inherently unstable, in time the particles aggregate, and form a precipitate. Lyiophilic sols, on the other hand, are more like true solutions in which the solute molecules are large and have an affinity for the solvent (e.g. starch in water). Association colloids are systems in which the dispersed phase consists of clusters of molecules that have lyophobic and lyophilic parts (e.g. soap in water).

supercritical carbon dioxide    →   superkritični ugljikov dioksid

Supercritical carbon dioxide (scCO₂) is a powerful, cheap, non-toxic and environmental friendly solvent. When used at a supercritical state (over 74 bar and 31 °C), it achieves similar solvating power as its organic competitors, such as hydrocarbons and chlorinated solvents. Supercritical carbon dioxide is one of few solvents that can be unrestrictedly used for food processing.

Solvay’s process    →   Solvayev postupak

Solvay ’s process is an industrial process for producing sodium carbonate from sodium chloride and ammonia and carbon dioxide.

Carbon dioixide is produced by the thermal decomposition of limestone, CaCO₃(s).

Quicklime, formed as a by-product of the thermal decomposition of limestone, is treated with water to form calcium hydroxide.

Calcium hydroxide is heated with ammonium chloride to form ammonia and calcium chloride (by product).

Carbon dioxide reacts with ammonia to form ammonium carbonate.

Ammonium carbonate further reacts with carbon dioxide to form ammonium bicarbonate.

Ammonium bicarbonate then react with sodium chloride to form sodium bicarbonate.

Dry sodium bicarbonate is heated in rotary furnace to give anhydrous sodium carbonate or soda ash.

The carbon dioxide produced is recycled back into the process.

technetium    →   tehnecij

Technetium was discovered by Carlo Perrier and Emilio Segre (Italy) in 1937. The origin of the name comes from the Greek word technikos meaning artificial. It is silvery-grey metal. Resists oxidation but tarnishes in moist air and burns in high oxygen environment. First synthetically produced element. Radioactive. Technetium is made first by bombarding molybdenum with deuterons (heavy hydrogen) in a cyclotron. Added to iron in quantities as low as 55 part-per-million transforms the iron into a corrosion-resistant alloy.

tellurium    →   telurij

Tellurium was discovered by Franz Joseph Muller von Reichstein (Romania) in 1782. The origin of the name comes from the Latin word tellus meaning earth. It is silvery-white, brittle semi-metal. Unreactive with water or HCl; dissolves in HNO₃; burns in air or oxygen. Tellurium is obtained as a by-product of copper and lead refining. Used to improve the machining quality of copper and stainless steel products and to colour glass and ceramics. Also in thermoelectric devices. Some is used in the rubber industry and it is a basic ingredient in manufacturing blasting caps.

vanadium    →   vanadij

Vanadium was discovered by A. M. del Rio (Spain) in 1801 and rediscovered by Nils Sefstrom (Sweden) in 1830. Named after Vanadis, the goddess of beauty in Scandinavian mythology. It is soft, ductile, silvery-white metal. Resistant to corrosion by moisture, air and most acids and alkalis at room temperature. Exposed surfaces form oxide coating. Reacts with concentrated acids. Vanadium is found in the minerals patronite (VS₄), vanadinite [Pb₅(VO₄)₃Cl] and carnotite [K₂(UO₂)₂(VO₄)₂·3H₂O]. Pure metal produced by heating with C and Cl to produce VCl₃ which is heated with Mg in Ar atmosphere. It is mixed with other metals to make very strong and durable alloys. Vanadium pentoxide (V₂O₅) is used as a catalyst, dye and fixer-fixer.