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497-19-8 solvay soda

Ammoniak-rest, m. ammonia residue (amidogen, NH2). -rohr, n. ammonia tube or pipe, -salpeter, m. ammonia saltpeter (ammonium nitrate), -salz, n. ammonium salt, -selfe,/. ammonia soap, -soda, /. ammonia soda, Solvay soda, -stickstoff, m. ammonia nitrogen. -verbindung, /, ammonia compound ammonium compound, -verfahren, n. ammonia process, -wasche, /. ammonia scrubbing ammonia recovery plant, -wascher,... [Pg.21]

After earning a lackluster Ph.D. from the University of Berlin in 1891, Haber wrote a friend, The thesis is miserable. One and a half years of new substances prepared like a baker s bread rolls.. . . One learns to be modest. In preparation for entering his father s business, he studied chemical technology in an alcohol distillery in Hungary, a Solvay soda factory in Austria, and a salt mine in Poland. His obligatory year in the Prussian army left him with a smart, military manner and a love of rank and discipline. His attempts to become a reserve officer failed, however, for this was a prestigious honor reserved for Christians, and Haber was Jewish. [Pg.59]

Synonyms The anhydrous salt Na2C03 also is called Solvay soda and soda ash (technical grade is about 99% purity). The decahydrate Na2C03 IOH2O also is known as washing soda or sal soda. These two names usually refer to the technical product. Other synonyms for the decahydrate are soda and Nevite. ... [Pg.861]

Alkaline milling The treatment is as in (a) but at 400 C. and in a bath containing 20 grams of Marseilles soap and 5 grams of Solvay soda per litre of distilled water. [Pg.517]

Anhydrous, Solvay soda. The technical grade (about 99% pure) is known as soda ash. Odorless, hygroscopic powder alkaline taste d 2.53. mp 851 but begins to lose C02 even at 400. On exposure to air it will gradually absorb one mo] water—about 15%. Sol in glycerol in 3.5 parts water at room temp, 2.2 parts water at 35°. Insol in alcohol. Dec by acids with effervescence. Combines with water with evolution of heat. Its aq soln is strongly alkaline. pH 11.6. Keep well closed. LDm (30 day) i.p. in mice 116.6 tng/kg (Norde). [Pg.1359]

OTHER names Anhydrous salt soda ash Solvay soda decahydrate sal soda washing soda (see Overview)... [Pg.729]

Early demand for chlorine centered on textile bleaching, and chlorine generated through the electrolytic decomposition of salt (NaCl) sufficed. Sodium hydroxide was produced by the lime—soda reaction, using sodium carbonate readily available from the Solvay process. Increased demand for chlorine for PVC manufacture led to the production of chlorine and sodium hydroxide as coproducts. Solution mining of salt and the avadabiHty of asbestos resulted in the dominance of the diaphragm process in North America, whereas soHd salt and mercury avadabiHty led to the dominance of the mercury process in Europe. Japan imported its salt in soHd form and, until the development of the membrane process, also favored the mercury ceU for production. [Pg.486]

These disadvantages prompted Ernest Solvay (1838—1922) to develop and commercialize a procedure using ammonia to produce soda ash from salt and limestone. The first plant using the Solvay process was built in 1863 this process or variations are in use in much of the world in the 1990s. [Pg.522]

The basic Solvay process remains the dominant production route for soda ash. Its continued success is based on the raw matedals, salt and limestone, being more readily available than natural alkaU. AH soda ash processes are based on the manipulation of saline phase chemistry (6,7) an understanding of which is important both to improving current processes and to the economic development of new alkaU resources. [Pg.522]

Akzo Process. Akzo Zout Chemie has developed a route to vinyl chloride and soda ash from salt usiag an amine—solvent system catalyzed by a copper—iodide mixture (13). This procedure theoretically requires half the energy of the conventional Solvay processes. [Pg.524]

The amount of soda ash, Na2C02, produced by the Solvay process has decreased, and most soda ash now comes from the Trona, Wyoming deposits (trona, Na2C02 NaHCO 2H20). Caustic soda, NaOH, solutions may be used ia wet batchiag processes as a source of soda (see Alkali and... [Pg.303]

Alkalies. In the 1960s, 3.2-34 x 10 t /yr of lime was captively produced by the U.S. alkaH industry for manufacturing soda ash and sodium bicarbonate via the Solvay process. Electrolytic process caustic soda and natural soda ash (trona) from Wyoming have largely replaced the Solvay process. Three of the trona producers in Wyoming now purchase quicklime for producing caustic soda. [Pg.178]

A.mmonia-Soda Process. Ammonium chloride is made as a by-product of the classic Solvay process, used to manufacture sodium carbonate (12,13) (see Alkali and chlorine products, sodium carbonate). The method iuvolves reaction of ammonia, carbon dioxide, and sodium chloride ia water... [Pg.364]

Vinylidene chloride monomer is produced commercially in the United States by The Dow Chemical Company and PPG Industries. The monomer is produced in Europe by Imperial Chemical Industries, Ltd., in the United Kingdom Badische Anilin und Soda Eabnk and Chemische Werk Hbls in Germany Solvay S.A. and Amaco et Compagnie in Erance and The Dow Chemical Company in the Netherlands. The monomer is produced in Japan by the Asahi Chemical Company, Kureha Chemical Industries, and Kanto Denka Kogyo Company. [Pg.440]

A former commercially important source of calcium chloride was as a by-product of the Solvay process used to produce soda ash (28). Because of environmental concerns and high energy costs, the Solvay process has been discontinued ia the United States though it is stiU used extensively elsewhere ia the world (see Calcium compounds). [Pg.410]

In 1976, over 3,000,000 tons of soda ash were produced in the United States using the Solvay process. This process has been discontinued in the United States because of pollution problems and high processing costs. It is stUl an important process in other countries. [Pg.413]

Sodium carbonate (soda ash) Solvay (ammonia-soda) Particulate matter Wet scrubbers... [Pg.498]

The Leblanc process was replaced by the ammonia soda (Solvay - 1860 ) process, in which sodium chloride brine is treated with ammonia and carbon dioxide to produce sodium bicarbonate and ammonium chloride. Sodium carbonate is obtained from the bicarbonate by heating. Ammonium chloride treated with lime gives calcium chloride and ammonia. The chlorine in the original salt becomes calcium chloride that is used for melting snow and ice. The ammonia is reused in the process (99.9% recovery). [Pg.263]

About 95% of the sodium carbonate used in the U.S. is mined, primarily in Wyoming. The ore is known as trona and needs only to be heated to produce commercial soda ash. Elsewhere in the world it is made by the Solvay process, which uses limestone and salt as raw materials. Calcium chloride is a byproduct of the Solvay process. [Pg.30]

EMC Corp., Solvay Minerals, General Chemical, OCI Wyoming, IMC, TG Soda Ash. [Pg.30]

This method of making soda ash is called the Solvay process. Discovered in 1861 by Belgian businessman Ernest Solvay (1838-1922), the Solvay process was used in the commercial production of soda ash in the 1870s, and it is still in use today. Soda ash is used in the manufacture of glass and soap. It is also used in the bleaching process for paper and cloth. [Pg.72]

Kiefer, David. Soda ash, Solvay style, American Chemical Society Web site. Available online. URL http //pubs.acs.org/ subscribe/journals/tcaw/1 l/i02/html/02chemchron.html. Accessed on March 17, 2008. [Pg.110]

Another indispensable carbonate is sodium carbonate, which is also known as soda ash. Centuries ago, impure sodium carbonate was obtained from the places where brine solutions had evaporated and from dry lake beds. The major source of soda ash today is once again from a natural source, but prior to 1985, it was synthesized in large quantities. The synthetic process most often used was the Solvay process, represented by the equations... [Pg.454]

Ammonia-soda Also called the Solvay process. A process for making sodium carbonate. The basic process was invented and partially developed in the first half of the 19th century by several workers, but the key invention was made by E. Solvay in Belgium in 1861. The first plant was built at Couillet, Belgium, in 1864 and thereafter the process became accepted worldwide, displacing the Leblanc process. The raw materials are limestone and salt calcium chloride is a waste product. The overall reaction is ... [Pg.21]

Schloesing-Rolland An early variant of the ammonia-soda process for making sodium carbonate. Operated near Paris in 1857 and then in Middlesbrough, England, for approximately 20 years until supplanted by the Solvay process. [Pg.236]

Solvay (1) An important process for making sodium carbonate, invented by E. Solvay in Belgium in 1861 and still used worldwide. See Ammonia-soda. [Pg.249]

Ammonia or its salts are employed in a variety of ways in many trades. From it nitric acid, the vital necessity for the manufacture of all high explosives, can be made it is an essential for the Brunner Mond or Solvay ammonia soda process for the production of alkali in the liquid form it is employed all over the world in refrigerating machinery, but its enormous and increasing use is in agfriculture, where, in the form of sulphate of ammonia, it constitutes one of, if not the most important chemical manures known to man. During the year 1916 350,000 tons of ammonium sulphate were produced in this country, the larger proportion of which was consumed in agriculture—a proportion likely to increase and not diminish if the demand for home production of food continues. [Pg.27]

Sodium carbonate (Na CO ) is the eleventh most used industrial chemical in the United States. It is commonly used as a bleaching agent and is manufactured in a two-step process. First, ammonia is combined with carbon dioxide to form sodium chloride and water, which reacts to form sodium bicarbonate and ammonium chloride (NH + CO + NaCl + H O —> NaHCOj + NH Cl). Sodium bicarbonate, commonly known as baking soda, is used as a leavening agent in baking, as an antacid to relieve stomach acid, and as a component for fire extinguishers. The second step is known as the Solvay process, wherein the sodium bicarbonate is heated and converted into sodium carbonate (NaHCO A— Na CO + H O + CO ). [Pg.52]


See other pages where 497-19-8 solvay soda is mentioned: [Pg.242]    [Pg.225]    [Pg.752]    [Pg.752]    [Pg.225]    [Pg.34]    [Pg.558]    [Pg.1090]    [Pg.36]    [Pg.95]    [Pg.208]    [Pg.242]    [Pg.225]    [Pg.752]    [Pg.752]    [Pg.225]    [Pg.34]    [Pg.558]    [Pg.1090]    [Pg.36]    [Pg.95]    [Pg.208]    [Pg.363]    [Pg.522]    [Pg.71]    [Pg.89]    [Pg.21]    [Pg.14]    [Pg.202]    [Pg.309]   
See also in sourсe #XX -- [ Pg.8 , Pg.861 ]




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