CHEMISTRY GLOSSARY

spontaneously combustible    →   samozapaljivi materijal

Spontaneously combustible materials are materials that can ignite without an external source of heat. Heat sufficient to reach the ignition temperature may be generated by reaction with oxygen in the air, by the absorption of moisture, from heat generated during processing, or even from radioactive decay.

fugacity    →   fugacitet

Fugacity (f) is a thermodynamic function used in place of partial pressure in reactions involving real gases and mixtures. For a component of a mixture, it is defined by

where μ is the chemical potential.

The fugacity of a gas is equal to the pressure if the gas is ideal. The fugacity of a liquid or solid is the fugacity of the vapour with which it is in equilibrium. The ratio of the fugacity to the fugacity in some standard state is the activity.

Gibbs free energy    →   Gibbsova slobodna energija

Gibbs free energy (G) is an important function in chemical thermodynamics, defined by

where H is the enthalpy, S the entropy, and T the thermodynamic temperature. Gibbs free energy is the energy liberated or absorbed in a reversible process at constant pressure and constant temperature. Sometimes called Gibbs energy and, in older literature, simply free energy.

Changes in Gibbs free energy, ΔG, are useful in indicating the conditions under which a chemical reaction will occur. If ΔG is negative the reaction will proceed spontaneously to equilibrium. In equilibrium position ΔG = 0.

graphite    →   grafit

Graphite is an allotrope of carbon. The atoms are arranged in layers as a series of flat, hexagonal rings. Graphite is a good conductor of heat and electricity. The layers cleave easily, making graphite useful as a solid lubricant. A process to make pure synthetic graphite was invented by the American chemist Edward Goodrich Acheson (1856–1931). The process consists of heating a mixture of clay (aluminum silicate) and powdered coke (carbon) in an iron bowl. The reaction involves the production of silicon carbide, which loses silicon at 4150 °C to leave graphite.

Haber process    →   Haberov proces

Haber process is an industrial process for producing ammonia by reaction of nitrogen with hydrogen:

The reaction is reversible and exothermic, so that a high yield of ammonia is favoured by low temperature. However, the rate of reaction would be too slow for equilibrium to be reached at normal temperatures, so an optimum temperature of about 450 °C is used, with a catalyst of iron containing potassium aluminium oxide promoters. The higher the pressure the greater the yield, although there are technical difficulties in using very high pressures. A pressure of about 250 atmospheres is commonly employed. The removal of ammonia from the batch as soon as it is formed ensures that an equilibrium favouring product formation is maintained. The nitrogen is obtained from air. Formerly, the hydrogen was from water gas and the water-gas shift reaction (the Bosch process) but now the raw material (called synthesis gas) is obtained by steam reforming natural gas.

The process is of immense importance for the fixation of nitrogen for fertilisers and explosives. It was developed in 1908 by German chemist Fritz Haber (1868-1934) and was developed for industrial use by Carl Bosch (1874-1940), hence the alternative name Haber-Bosch process.

substitution    →   supstitucija

Substitution (substitution reaction) is a reaction in which an atom or fragment within a molecule is replaced with another atom or a fragment.

half-life of a reactant    →   poluživot reaktanta

For a given reaction the half-life, t_1/2, of a reactant is the time required for its concentration to reach a value that is the arithmetic mean of its initial and final (equilibrium) value.

Half-life is constant for first-order reactions.

Half-life is not constant for second-order reactions but rather it varies with initial concentration and k.

hemiacetal    →   poluacetal

Hemiacetals are organic compounds having the general formula R₂C(OH)OR’ (R’ ≠ H), derived from aldehydes or ketones by formal addition of an alcohol to the carbonyl group. Hemiacetals are generally unstable compounds. In some cases however, stable cyclic hemiacetals can be readily formed, especially when 5- and 6-membered rings are possible. In this case an intramolecular OH group reacts with the carbonyl group. Glucose and many other aldoses exist as cyclic hemiacetals whereas fructose and similar ketoses exist as cyclic hemiketals. Originally, the term was confined to derivatives of aldehydes (one R = H), but it now applies equally to derivatives of ketones (neither R = H).

hemiketal    →   poluketal

Hemiketals are organic compounds having the structure R₂C(OH)OR (R ≠ H), derived from ketones by formal addition of an alcohol to the carbonyl group. The rings of ketose sugars are hemiketals. This term, once abandoned, has been reinstated as a subclass of hemiacetals.

substrate    →   supstrat

1. Substrate is a surface upon which an organism grows, sometimes by using chemicals of particles in the material as food

2. Substrate is a substance that is acted upon by an enzyme during a biochemical reaction.

3. Substrate is the material or product that is to be coated (for example, paint or laminate.).