Monday, February 16, 2009

soap


soap a cleansing agent. It cleanses by lowering the surface tension of water, by emulsifying grease, and by absorbing dirt into the foam. Ancient peoples are believed to have employed wood ashes and water for washing and to have relieved the resulting irritation with grease or oil. In the 1st cent. AD, Pliny described a soap of tallow and wood ashes used by Germanic tribes to brighten their hair. A soap factory and bars of scented soap were excavated at Pompeii. Soap fell into disuse after the fall of Rome but was revived in Italy probably in the 8th cent. and reached France c.1200; Marseilles became noted as a soapmaking center. Although soap was known in England in the 14th cent., the first English patent to a soapmaker was issued in the 17th cent. The industry was handicapped in England from 1712 to 1853 by a heavy tax on soap. In the American colonies soap factories appeared at an early date, and many housewives made soap from waste fats and lye (obtained by leaching wood ashes). The manufacture of soap was stimulated by Chevreul's discovery of oleic and stearic acids in the early 19th cent. and by Leblanc's method (1791) of preparing soda from salt. Chemically, soaps are metallic salts of fatty acids . The manufacture of soap is based on a chemical reaction (saponification) in which an alkali acts upon a fat to form a metal salt (soap) and an alcohol (glycerol). A number of methods may be employed to make soap, but all are based on the same principle of operation. Fats and oils (often blended) are heated in a large vessel, then enough alkali to react with all the fat is stirred in. Salt is added, and the soap then forms a light curd that floats to the surface. Glycerol, a valuable byproduct, can be distilled from the liquid residue. To produce a purer soap, the curds are washed with salt solution, water is later added, and the solution is allowed to settle; the upper of the two layers thus formed is the pure soap, called settled soap. It is thoroughly churned, poured into huge frames, cut with wires, shaped, and stamped. Hard-milled soap is run over chilled rollers and is scraped off as chips which are rolled into ribbons, cut, and shaped. Soap is marketed also as chips, flakes, and beads and in powdered form. Soap powders, as distinguished from powdered soap, contain builders that assist in rough cleaning. Soaps differ according to the lathering properties of the fat or oils and according to the alkali employed. When sodium hydroxide is used as the alkali, hard soaps are formed; potassium hydroxide yields soft soaps. Aluminum, calcium, magnesium, lead, or other metals are used in place of sodium or potassium for soaps used in industry as paint driers, ointments, and lubricating greases and in waterproofing. Fillers are added to many soaps to increase lathering, cleansing, and water-softening properties; the sodium salt of rosin is commonly used in yellow laundry soap to increase lathering. Soap substitutes include saponin-containing plants such as soapwort and shagbark and the modern soapless detergents (usually sulfonated alcohols), which may be used in hard water and even in saltwater without forming curds

aspartic acid


aspartic acid , organic compound, one of the 20 amino acids commonly found in animal proteins. Only the l -stereoisomer participates in the biosynthesis of proteins. Its acidic side chain adds a negative charge and hence a greater degree of water-solubility to proteins in neutral solution and has been shown to be near the active sites of some enzymes (see pepsin ). Aspartic acid is not essential to the human diet. It was discovered in protein in 1868.

benzoic acid


benzoic acid , C 6 H 5 CO 2 H, crystalline solid organic acid that melts at 122°C and boils at 249°C. It is the simplest aromatic carboxylic acid (see aryl group and carboxyl group ). In addition to being synthesized from a variety of organic compounds (e.g., benzyl alcohol, benzaldehyde, toluene, and phthalic acid), it may be obtained from resins, notably gum benzoin . It is used largely for making its salts and esters, most notably sodium benzoate, which is widely used as a preservative in foods and beverages and as a mild antiseptic in mouthwashes and toothpastes.

acid-base indicators


acid-base indicators organic compounds that, in aqueous solution, exhibit color changes indicative of the acidity or basicity of the solution. Common indicators include p -nitrophenol, which is colorless from p H 1 to 5 and yellow from p H 5 to 9; methyl orange, yellow in basic and neutral solutions and reddish below p H 3.7; phenolphthalein, colorless in acid and neutral solutions, pink at about p H 8.5, and purplish at p H 10; and litmus . Most indicators are also used in large amounts for dyeing; small quantities are nonetheless invaluable for use as indicators in chemical laboratories

acids and bases


acids and bases two related classes of chemicals; the members of each class have a number of common properties when dissolved in a solvent, usually water. Properties Acids in water solutions exhibit the following common properties: they taste sour; turn litmus paper red; and react with certain metals, such as zinc, to yield hydrogen gas. Bases in water solutions exhibit these common properties: they taste bitter; turn litmus paper blue; and feel slippery. When a water solution of acid is mixed with a water solution of base, water and a salt are formed; this process, called neutralization , is complete only if the resulting solution has neither acidic nor basic properties. Classification Acids and bases can be classified as organic or inorganic. Some of the more common organic acids are: citric acid , carbonic acid , hydrogen cyanide , salicylic acid, lactic acid , and tartaric acid . Some examples of organic bases are: pyridine and ethylamine. Some of the common inorganic acids are: hydrogen sulfide , phosphoric acid , hydrogen chloride , and sulfuric acid . Some common inorganic bases are: sodium hydroxide , sodium carbonate , sodium bicarbonate , calcium hydroxide , and calcium carbonate . Acids, such as hydrochloric acid, and bases, such as potassium hydroxide, that have a great tendency to dissociate in water are completely ionized in solution; they are called strong acids or strong bases. Acids, such as acetic acid, and bases, such as ammonia, that are reluctant to dissociate in water are only partially ionized in solution; they are called weak acids or weak bases. Strong acids in solution produce a high concentration of hydrogen ions, and strong bases in solution produce a high concentration of hydroxide ions and a correspondingly low concentration of hydrogen ions. The hydrogen ion concentration is often expressed in terms of its negative logarithm, or p H (see separate article). Strong acids and strong bases make very good electrolytes (see electrolysis ), i.e., their solutions readily conduct electricity. Weak acids and weak bases make poor electrolytes. See buffer ; catalyst ; indicators, acid-base ; titration . Acid-Base Theories There are three theories that identify a singular characteristic which defines an acid and a base: the Arrhenius theory, for which the Swedish chemist Svante Arrhenius was awarded the 1903 Nobel Prize in chemistry; the Brönsted-Lowry, or proton donor, theory, advanced in 1923; and the Lewis, or electron-pair, theory, which was also presented in 1923. Each of the three theories has its own advantages and disadvantages; each is useful under certain conditions. The Arrhenius Theory When an acid or base dissolves in water, a certain percentage of the acid or base particles will break up, or dissociate (see dissociation ), into oppositely charged ions. The Arrhenius theory defines an acid as a compound that can dissociate in water to yield hydrogen ions, H + , and a base as a compound that can dissociate in water to yield hydroxide ions, OH - . For example, hydrochloric acid, HCl, dissociates in water to yield the required hydrogen ions, H + , and also chloride ions, Cl - . The base sodium hydroxide, NaOH, dissociates in water to yield the required hydroxide ions, OH - , and also sodium ions, Na + . The Brönsted-Lowry Theory Some substances act as acids or bases when they are dissolved in solvents other than water, such as liquid ammonia. The Brönsted-Lowry theory, named for the Danish chemist Johannes Brönsted and the British chemist Thomas Lowry, provides a more general definition of acids and bases that can be used to deal both with solutions that contain no water and solutions that contain water. It defines an acid as a proton donor and a base as a proton acceptor. In the Brönsted-Lowry theory, water, H 2 O, can be considered an acid or a base since it can lose a proton to form a hydroxide ion, OH - , or accept a proton to form a hydronium ion, H 3 O + (see amphoterism ). When an acid loses a proton, the remaining species can be a proton acceptor and is called the conjugate base of the acid. Similarly when a base accepts a proton, the resulting species can be a proton donor and is called the conjugate acid of that base. For example, when a water molecule loses a proton to form a hydroxide ion, the hydroxide ion can be considered the conjugate base of the acid, water. When a water molecule accepts a proton to form a hydronium ion, the hydronium ion can be considered the conjugate acid of the base, water. The Lewis Theory Another theory that provides a very broad definition of acids and bases has been put forth by the American chemist Gilbert Lewis. The Lewis theory defines an acid as a compound that can accept a pair of electrons and a base as a compound that can donate a pair of electrons. Boron trifluoride, BF 3 , can be considered a Lewis acid and ethyl alcohol can be considered a Lewis base.

amino acid


amino acid , any one of a class of simple organic compounds containing carbon, hydrogen, oxygen, nitrogen, and in certain cases sulfur. These compounds are the building blocks of proteins. They are characterized by the presence of a carboxyl group (COOH) and an amino group (NH 2 ) attached to the same carbon at the end of the compound. The 20 amino acids commonly found in animals are alanine , arginine , asparagine , aspartic acid , cysteine , glutamic acid , glutamine , glycine , histidine , isoleucine , leucine , lysine , methionine , phenylalanine , proline , serine , threonine , tryptophan , tyrosine , and valine . More than 100 less common amino acids also occur in biological systems, particularly in plants. Every amino acid except glycine can occur as either of two optically active stereoisomers, d or l ; the more common isomer in nature is the l -form. When the carboxyl carbon atom of one amino acid covalently binds to the amino nitrogen atom of another amino acid with the release of a water molecule, a peptide bond is formed. Amino acids are released in the intestinal tract by the digestion of food proteins and are then carried in the bloodstream to the body cells, where they are used for growth, maintenance, and repair. Cellular catabolism breaks amino acids down into smaller fragments. Many of the amino acids necessary in metabolism can be synthesized in the human or animal body when needed; these are called nonessential. Others cannot be synthesized in sufficient quantities; these are termed essential and must be provided in the diet.

butyric acid


butyric acid or butanoic acid , CH 3 CH 2 CH 2 CO 2 H, viscous, foul-smelling, liquid carboxylic acid; m.p. about -5°C; b.p. 163.5°C. It is miscible with water, ethanol, and ether. It is a low molecular weight fatty acid that is present in butter as an ester of glycerol; the odor of rancid butter is due largely to the presence of free butyric acid. Butyric acid is used in the manufacture of plastics. Isobutyric acid, or 2-methylpropanoic acid, (CH 3 ) 2 CHCO 2 H, is a geometric isomer of the butyric acid described above; it has different physical properties but similar chemical properties