- Solvay process
The Solvay process, also referred to as the ammonia-soda process, is the major industrial process for the production of "
soda ash" ( sodium carbonate). The ammonia-soda process was developed into its modern form by Ernest Solvayduring the 1860s. The ingredients for this process are readily available and inexpensive: salt brine (from inland sources or from the sea) and limestone(from mines). The worldwide production of soda ash in 2005 has been estimated at 42 billion kilograms (92 billion pounds),Kostick, Dennis (2006). [http://minerals.usgs.gov/minerals/pubs/commodity/soda_ash/soda_myb05.pdf "Soda Ash"] , chapter in "2005 Minerals Yearbook," United States Geological Survey. See Table I.] which is more than six kilograms per year for each person on earth. Solvay-based chemical plants now produce roughly three-fourths of this supply, with the remainder being mined from natural deposits.
The Solvay process produces soda ash (predominantly
sodium carbonate(Na2CO3)) from brine(as a source of sodium chloride(NaCl)) and from limestone(as a source of calcium carbonate(CaCO3)).cite journal | author = Kiefer, David M. | url= http://www.webcitation.org/5WGM2f75m | title = Soda Ash, Solvay Style | journal = Today's Chemist at Work | volume = 11 | issue = 2 | month = February | year = 2002 | pages = 87–88, 90 Online version archived at WebCite from [http://pubs.acs.org/subscribe/journals/tcaw/11/i02/html/02chemchron.html this original URL] on 2008-03-12.] The overall process is:
:2 NaCl + CaCO3 → Na2CO3 + CaCl2
The actual implementation of this global, overall reaction is intricate. [cite book |last=Speight |first=James |title= Chemical Process and Design Handbook |year=2001 |publisher=McGraw Hill | isbn = 0071374337 | doi = 10.1036/0071374337] [http://www.webcitation.org/5W0IxdohY "Process Best Practices Reference Document (BREF) for Soda Ash,"] report produced by the [http://www.cefic.be/templates/shwAssocDetails.asp?NID=473&HID=27&ID=60 European Soda Ash Producer's Association] , March 2004. Archived at WebCite from [http://www.cefic.be/files/Publications/ESAPA_Soda_Ash_Process_BREF3.pdf this original URL] on 2008-03-01.] [cite book |last=Moore |first=John T. Edd |title=Chemistry Made Simple |year=2005 |publisher=Broadway Books |location= |isbn = 0767917022 | pages=190] A simplified description can be given using the four different, interacting chemical reactions illustrated in the figure. In the first step in the process,
carbon dioxide(CO2) passes through a concentrated aqueous solution of sodium chloride (NaCl) and ammonia(NH3).
In industrial practice, the reaction is carried out by passing concentrated brine through two towers. In the first, ammonia bubbles up through the brine and is absorbed by it. In the second, carbon dioxide bubbles up through the ammoniated brine, and
sodium bicarbonate(NaHCO3) precipitates out of the solution. Note that, in a basic solution, NaHCO3 is less water-soluble than sodium chloride. The ammonia (NH3) buffers the solution at a basic pH; without the ammonia, a hydrochloric acidbyproduct would render the solution acidic, and arrest the precipitation.
The necessary ammonia "catalyst" for reaction (I) is reclaimed in a later step, and relatively little ammonia is consumed. The carbon dioxide required for reaction (I) is produced by heating ("
calcination") of the limestone at 950 - 1100 °C. The calcium carbonate (CaCO3) in the limestone is partially converted to quicklime(calcium oxide (CaO)) and carbon dioxide:
The sodium bicarbonate (NaHCO3) that precipitates out in reaction (I) is filtered out from the hot ammonium chloride (NH4Cl) solution, and the solution is then reacted with the
quicklime(calcium oxide (CaO)) left over from heating the limestone in step (II).
CaO makes a strong basic solution. The ammonia from reaction (III) is recycled back to the initial brine solution of reaction (I).
The sodium bicarbonate (NaHCO3) precipitate from reaction (I) is then converted to the final product, sodium carbonate (Na2CO3), by calcination (160 - 230 C), producing water and carbon dioxide as byproducts:
The carbon dioxide from step (IV) is recovered for re-use in step (I). When properly designed and operated, a Solvay plant can reclaim almost all its ammonia, and consumes only small amounts of additional ammonia to make up for losses. The only major inputs to the Solvay process are salt, limestone and thermal energy, and its only major byproduct is
calcium chloride, which is sold as road salt.
Uses of Soda Ash
Soda ash is used in many industrial processes, and its production is sometimes used as an indicator of economic health. The principal current uses include:
*Glass making: More than half the worldwide production of soda ash is used to make glass. Bottle and window glass (
Soda-lime glass) is made by melting a mixture of sodium carbonate, calcium carbonate and silica sand ( silicon dioxide(SiO2)).
*Water treatment: Sodium carbonate is used to soften water (precipitates out Mg2+ and Ca2+ carbonates). This is used both industrially and domestically (in some washing powders).
*Making soaps and detergents: Often sodium carbonate is used as a cheaper alternative to lye (
*Paper making: Sodium carbonate is used to make
sodium bisulfite(NaHSO3) for the "sulfite" method of separating ligninfrom cellulose.
*As a common base in many chemical factories because it is cheaper than NaOH and far safer to handle.
sodium bicarbonate: NaHCO3 is used in baking soda and fire extinguishers. Although NaHCO3 is produced in the Solvay process, heating it to remove the ammonia it is contaminated with decomposes some NaHCO3, so it is actually cheaper to react the finished Na2CO3 product with CO2.
sulfur dioxide(SO2) from flue gases in power stations. This is becoming more common, especially where stations have to meet stringent emission controls.
The name "soda ash" is based on the principal historical method of obtaining alkali, which was by using water to extract it from ashes. Wood fires yielded potash and the active ingredient
potassium carbonate. The word "soda" (from the Middle Latin) originally referred to certain plants that grow in salt marshes; it was discovered that the ashes of these plants yielded the useful alkali "soda ash." The cultivation of such plants for production of soda ash reached a particularly high state of development in the 18th Century in Spain, where the plants are named "barrilla"; the English word is " barilla." [The barilla used for soda ash production refers to any of several bushy plants that are well adapted to grow in salt marshes, and that are common in Spain and Italy. The ashes of these plants can contain as much as 30% sodium carbonate. The principal species for soda ash production were the " saltworts" " Salsola soda" or " Salsola kali", but several other species could also be used.] [Pérez, Joaquín Fernández (1998). [http://www.webcitation.org/5W0IroD9s "From the barrilla to the Solvay factory in Torrelavega: The Manufacture of Saltwort in Spain,"] "Antilia: The Spanish Journal of History of Natural Sciences and Technology," Vol. IV, Art. 1. ISSN 1136-2049. Archived by WebCite from [http://www.ucm.es/info/antilia/revista/vol4-en/ant4-1-en.htm this original URL] on 2008-03-01.] [Grieve, M. (1931). "A Modern Herbal," ISBN 0-486-22798-7 & 0486227995. See section on [http://www.botanical.com/botanical/mgmh/g/glassw18.html glasswort] . Retrieved October 21, 2005.] The ashes of kelpalso yield soda ash, and were the basis of an enormous 18th Century industry in Scotland. Alkali was also mined from dry lakebeds in Egypt.
By the late 1700s, however, these sources were insufficient to meet Europe's burgeoning demand for alkali for soap, textile, and glass industries.cite journal | author = Kiefer, David M. | url = http://www.webcitation.org/5WGKqjQ7q | title = It was all about alkali | journal = Today's Chemist at Work | volume = 11 | issue = 1 | pages = 45–6 Online version archived at WebCite from [http://pubs.acs.org/subscribe/journals/tcaw/11/i01/html/01chemchron.html this original URL] on 2008-03-12.] In 1791, the French physician
Nicolas Leblancdeveloped a method to manufacture soda ash using salt, limestone, sulfuric acid, and coal. Although the Leblanc processcame to dominate alkali production in the early 1800s, the expense of its inputs and its polluting byproducts (including hydrochloric acidgas) made it apparent that it was far from an ideal solution.
It has been reported that, in 1811, the renowned French physicist
Augustin Jean Fresneldiscovered that sodium bicarbonate precipitates when carbon dioxide is bubbled through ammonia-containing brine— which is the chemical reaction central to the Solvay process. The discovery wasn't published. As has been noted by Desmond Reilly, "The story of the evolution of the ammonium-soda process is an interesting example of the way in which a discovery can be made and then laid aside and not applied for a considerable time afterwards." [cite journal | author = Reilly, Desmond | month = December | year = 1951 | title = Salts, Acids & Alkalis in the 19th Century. A Comparison between Advances in France, England & Germany | journal = Isis | volume = 42 | issue = 4 | pages = 287–296 | url = http://links.jstor.org/sici?sici=0021-1753%28195112%2942%3A4%3C287%3ASA%26AIT%3E2.0.CO%3B2-6 | doi = 10.1086/349348] Serious consideration of this reaction as the basis of an industrial process dates from the British patent issued in 1834 to H. G. Dyan and J. Henning. There were several attempts to reduce this reaction to industrial practice, with varying success.
In 1861, the Belgian industrial chemist
Ernest Solvayturned his attention to the problem; he was apparently largely unaware of the extensive earlier work. His solution, an 80-foot-tall gas absorption tower in which carbon dioxide bubbled up through a descending flow of brine, together with efficient recovery and recycling of the ammonia, proved effective, and by 1864, Solvay and his brother Alfred had acquired good financial backing and constructed a plant in the Belgian town of Charleroi. The new process proved more economical and less polluting than the Leblanc method, and its use spread. In 1874, the Solvays expanded their facilities with a new, larger plant at Nancy, France.
In the same year,
Ludwig Mondvisited Solvay in Belgium and acquired rights to use the new technology. He and John Brunner formed the firm of Brunner, Mond & Co., and built a Solvay plant at Winnington, near Northwich, Cheshire, England. The facility started up in 1874. Mond was instrumental in making the Solvay process a commercial success; he made several refinements between 1873 and 1880 that removed byproducts that could slow or halt the mass production of sodium carbonate through use of the process.
In 1884, the Solvay brothers licensed Americans William B. Cogswell and Rowland Hazard to produce soda ash in the United States, and formed a joint venture (
Solvay Process Company) to build and operate a plant in Solvay, New York.
By the 1890s, Solvay process plants produced the majority of the world's soda ash.
In 1938, large natural deposits of the mineral
Tronawere discovered near the Green River in Wyoming. Sodium carbonate can be mined from this source less expensively than it can be produced by the Solvay process, and with the closing of the original Solvay, New York plant in 1986, there have been no Solvay-based plants operating in North America. Throughout the rest of the world, however, the Solvay process remains the major source of soda ash.
Byproducts and Wastes
The principal byproduct of the Solvay process is
calcium chloride(CaCl2) in aqueous solution. The process has other waste and byproducts as well. Not all of the limestone that is calcined is converted to quicklime and carbon dioxide (in reaction II); the residual calcium carbonate and other components of the limestone becomes wastes. In addition, the salt brine used by the process is usually purified to remove magnesium and calcium ions, typically to form carbonates; otherwise, these impurities would lead to scale in the various reaction vessels and towers. These carbonates are additional waste products.
In inland plants, such as that in
Solvay, New York, the byproducts have been deposited in "waste beds;" the weight of material deposited in these waste beds exceeded that of the soda ash produced by about 50%. These waste beds have led to water pollution, principally by calcium and chlorine ions. The waste beds in Solvay, New York substantially increased the salinity in nearby Onondaga Lake, which is among the most polluted lakes in the U.S. [ [http://www.onlakepartners.org/p12036.html Onondaga Lake Partnership] . Retrieved 2006-10-14.] and is a superfundpollution site. [U.S. Environmental Protection Agency, superfund [http://cfpub.epa.gov/supercpad/cursites/csitinfo.cfm?id=0203382 ID NYD986913580] . Retrieved 2006-10-14.] As such waste beds age, they do begin to support plant communities which have been the subject of several scientific studies. [Cohn, E.V.J., Rostanski, A., Tokarska-Guzik, B., Trueman, I.C., and Wozniak, G. (2001). "The flora and vegetation of an old Solvay process tip in Jaworzno (Upper Silesia, Poland)." "ActaSoc. Bot. Pol." 70(1):47-60.] [Michalenko, Edward M. (1991). "Pedogenesis and invertebrate microcommunity succession in immature soils originating from chlor-alkali wastes," doctoral dissertation, College of Environmental Science and Forestry, State University of New York.]
At seaside locations, such as those at Saurashtra, Gujarat, India, [ [http://www.webcitation.org/5W0KjAKfk "Technology in the Indian Soda Ash Industry"] , Technology Status Report #148 (October, 1995), [http://dsir.nic.in Department of Scientific and Industrial Research] , Ministry of Science & Technology, India. Archived by WebCite from [http://dsir.nic.in/reports/techreps/tsr148.pdf this original URL] on 2008-03-01.] and at
Osborne, South Australia, [ [http://www.penrice.com.au/company.htm "Penrice Soda Holdings Limited"] . Retrieved 2006-10-14.] the CaCl2 solution may be discharged directly into the sea, apparently without substantial environmental harm. In the "modified" Solvay process, the CaCl2 is supplanted by ammonium chloride(NH4Cl). NH4Cl, which can be used in fertilizer, may have greater commercial value than CaCl2, thus reducing the extent of waste beds.
Carbon Sequestration and the Solvay Process
Variations in the Solvay process have been proposed for carbon sequestration. One idea is to react carbon dioxide, produced perhaps by the combustion of coal, to form solid carbonates (such as sodium bicarbonate) that could be permanently stored, thus avoiding carbon dioxide emission into the atmosphere. [Huijgen, W.J.J. and Comans, R.N.J. (February, 2003). [http://www.ecn.nl/docs/library/report/2003/c03016.pdf "Carbon dioxide sequestration by mineral carbonation: Literature Review,"] Report ECN C-03-016, [http://www.edn.nl/en/ Energy Research Centre of the Netherlands] . Retrieved 2006-10-14.] [Cite journal | volume = 27 | issue = 1 | pages = 193–232 | last = Lackner | first = Klaus S | title = Carbonate Chemistry for Sequestering Fossil Carbon | journal = Annual Review of Energy and the Environment | year = 2002 | doi = 10.1146/annurev.energy.27.122001.083433] Variations in the Solvay process have been proposed to convert carbon dioxide emissions into sodium carbonates, but carbon sequestration by calcium or magnesium carbonates appears more promising.
* [http://www.cefic.be/Templates/shwAssocDetails.asp?NID=473&HID=27&ID=60 European Soda Ash Producer's Association (ESAPA)]
* [http://www.clrc.org/solvay/splsproom.htm Solvay Process Collection, Solvay (New York) Public Library.]
* [http://www.onondaganation.org/etimeline.pdf Timeline of US plant at Solvay, New York]
* [http://www.saltsense.co.uk/hist-chem11.htm Salt and the Chemical Revolution]
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