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After World War

The next phase which resulted in the worldwide acceptance of eddy current technology for testing metals was the work of Dr Friedrich Foerster. Dr Foerster, a modem Giant, has rightly been called the father of modern eddy current testing (Ref 5). His early work was driven by the priorities of the Second World War, after which he embarked upon major research and... [Pg.272]

A few last details may be given about Keyes, which should further demonstrate the crucial importance of the evolution of organic industries immediately after the first world war. After studying under G. N. Lewis, Keys focused not only on lacquers, as we have seen, but also on synthetic dyes. Later on, he moved toward petroleum chemistry and specialized in problems of molecular cracking because he also had a good deal of experience in distillation processes while he worked for the U.S. Industrial Alcohol Company of New York in the early 1920s (43). [Pg.65]

Heidi and her grandfather in the Swiss Alps, the provincialism of Swiss cities, and the obsession with order and common sense have hardly been conducive to the development of modernism in Switzerland. In European modernist literature, Switzerland tends to serve as the model for a pre-modern, idyllic vision of life that European writers often invoked as a refuge from the chaos of the modern metropolis. Yet Zurich, the largest Swiss city, was the center of European modernism during the two world wars. After these two invasions of modernist writers, artists, composers, dancers, and theater people, the Swiss launched their own modernism after 1945. [Pg.204]

LDPE attained rapid popularity due to its electrical insulating properties, which were exploited for the development of radar technology during the Second World War. After the discovery of LD PE s excellent film forming properties in the late 1940s, a sudden increase in demand took place, which triggered the worldwide commercialization of the resin and related technologies. [Pg.77]

World War after which he joined the Pasteur Institut in Paris, becoming its head in 1954 and director in 1971. He was professor of molecular biology at the College de France from 1967. The Monod equation describing the kinetics tor molecular growth is named after him. [Pg.244]

Titanium is not a rare element it is the most abundant transition metal after iron, and is widely distributed in the earth s surface, mainly as the dioxide TiOj and ilmenite FeTi03. It has become of commercial importance since World War II mainly because of its high strength-weight ratio (use in aircraft, especially supersonic), its... [Pg.369]

After World War II the International Union of Chemistry became the International Union of Pure and Applied Chemistry (known in the chemical com munity as the lUPAC) Since 1949 the lUPAC has is sued reports on chemical nomenclature on a regular basis The most recent lUPAC rules for organic chem istry were published in 1993 The lUPAC rules often offer several different ways to name a single com pound Thus although it is true that no two com... [Pg.78]

Ma.nufa.cture. AU. manufacturers of butynediol use formaldehyde ethynylation processes. The earliest entrant was BASF, which, as successor to I. G. Farben, continued operations at Ludwigshafen, FRG, after World War II. Later BASF also set up a U.S. plant at Geismar, La. The first company to manufacture in the United States was GAF in 1956 at Calvert City, Ky., and later at Texas City, Tex., and Seadrift, Tex. The most recent U.S. manufacturer is Du Pont, which went on stream at La Porte, Tex., about 1969. Joint ventures of GAF and Hbls in Mad, Germany, and of Du Pont and Idemitsu in Chiba, Japan, are the newest producers. [Pg.106]

Ma.nufa.cture. Butyrolactone is manufactured by dehydrogenation of butanediol. The butyrolactone plant and process in Germany, as described after World War II (179), approximates the processes presendy used. The dehydrogenation was carried out with preheated butanediol vapor in a hydrogen carrier over a supported copper catalyst at 230—250°C. The yield of butyrolactone after purification by distillation was about 90%. [Pg.111]

From 1910 onward waste filament yam had been chopped into short lengths suitable for use on the machinery designed to process cotton and wool staples into spun yams. In the 1930s new plants were built specifically to supply the staple fiber markets. During World War II the production of staple matched that of filament, and by 1950, staple viscose was the most important product. The new spun-yam oudets spawned a series of viscose developments aimed at matching the characteristics of wool and cotton more closely. Viscose rayon was, after all, silk-like. Compared with wool it lacked bulk, residence, and abrasion resistance. Compared to cotton, it was weaker, tended to shrink and crease more easily, and had a rather lean, limp hand. [Pg.345]

AH these early inflation processes (41) were difficult to control, and after World War 11 they were neglected until the 1960s. Companies in Japan, the United States, and Europe then started to develop inflated—collapsed rayons (Eig. 5b) for speciaUty papers (42) and wet-laid nonwovens. [Pg.350]

Fluorine was first produced commercially ca 50 years after its discovery. In the intervening period, fluorine chemistry was restricted to the development of various types of electrolytic cells on a laboratory scale. In World War 11, the demand for uranium hexafluoride [7783-81-5] UF, in the United States and United Kingdom, and chlorine trifluoride [7790-91 -2J, CIF, in Germany, led to the development of commercial fluorine-generating cells. The main use of fluorine in the 1990s is in the production of UF for the nuclear power industry (see Nuclearreactors). However, its use in the preparation of some specialty products and in the surface treatment of polymers is growing. [Pg.122]

Liquid Fuels via Methanol Synthesis and Conversion. Methanol is produced catalyticaHy from synthesis gas. By-products such as ethers, formates, and higher hydrocarbons are formed in side reactions and are found in the cmde methanol product. Whereas for many years methanol was produced from coal, after World War II low cost natural gas and light petroleum fractions replaced coal as the feedstock. [Pg.82]

Although a few simple hydrides were known before the twentieth century, the field of hydride chemistry did not become active until around the time of World War II. Commerce in hydrides began in 1937 when Metal Hydrides Inc. used calcium hydride [7789-78-8J, CaH2, to produce transition-metal powders. After World War II, lithium aluminum hydride [16853-85-3] LiAlH, and sodium borohydride [16940-66-2] NaBH, gained rapid acceptance in organic synthesis. Commercial appHcations of hydrides have continued to grow, such that hydrides have become important industrial chemicals manufactured and used on a large scale. [Pg.297]

In the second quarter of the twentieth century, with the development of poly(vinyl chloride), nylon, polyurethane, and other polymers, many new and improved leather-like materials, so-called coated fabrics (qv), were placed on the market. Shortages of leather after World War 11 led to the expansion of these leather-like materials ("man-made" leathers) to replace leather in shoes, clothing, bags, upholstery, and other items. DurabiUty and waterproof quahties superior to leather made coated fabrics advantageous, in spite of imperfection in breathabihty and flexibiUty. Demands for shoes, clothing, and other items are stiU increasing due to growing world population and urbanization. [Pg.88]

Vinyl-Coated Fabrics. Leather substitutes are designed to imitate the appearance of leather with its grain surface. This requirement has been accomphshed by coating substances that are capable of forming a uniform film, and was first met by plasticized poly(vinyl chloride) (PVC). A leather-like material termed vinyl-coated fabric was developed in the 1930s in the United States and Germany. Shortages of leather after World War 11 spurred the expansion of this material. [Pg.89]

Many kilns that formerly were direct coal-fired or producer-gas verticals were retrofitted to natural gas firing with center-burners and after World War II, dramatically improving lime quaUty, kiln capacity, and fuel efficiency. By the 1960s, this improved vertical kiln had lost favor to rotary and other special kilns because of the supply and cost problems of oil and gas in the United States and the spectacular improvement in rotary kiln performance. Many natural gas-fired center burners were permanently closed and dismanded because they could not be converted to coal. However, the reverse occurred in Europe where the extensive oil and gas discoveries heightened interest in the new, advanced vertical kilns. [Pg.173]

Lime stabilization originated in Texas after World War II, and now it is used throughout the world. Lime is most commonly applied at a 4 wt % application or ca 11 kg/m (20 Ib/yd ) for 15 cm of compacted depth. It can be applied dry as hydrated time or granular quicklime or as a wet slurry. Distribution of the latter form is dusfless. Copious amounts (as much as 5—10%) of water are always needed in excess of the optimum moisture content of the soil. Then, a requisite for success is intimate mixing with a rotary mixer, followed by compaction to a minimum of 95% Proctor density. [Pg.177]


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