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Low-temperature developers

Ifpexol A process for removing water and acid gases from hydrocarbon gas streams by washing with a proprietary solvent at a very low temperature. Developed by the Institut Frangais du Petrole. [Pg.144]

At temperatures below 50F/10C hydroquinone developers are inactive. It is extremely susceptible to the action of bromide. When compounded with alkali carbonates it gives a slow-working but high contrast developer. With caustic alkali (e.g., sodium hydroxide) its action is very rapid, with the highest possible contrast. For this reason, it is the most widely used developer for technical applications, especially in process work where the highest attainable contrast is essential. In the presence of caustic alkali (i.e., high pH) it is not temperature-sensitive and can be used for low-temperature developing. Hydroquinone developers keep well and are slowly exhausted. [Pg.182]

Time-temperature development chart for low-temperature developers. This chart shows time-temperature for low-temperature developers labeled as follows (l) Kodak SD-22 Amidol-Pyrocatechin, no glycol (2) Kodak SD-22, 25% glycol (3) Kodak SD-22, 50% glycol (4) Kodak D-8, no glycol ... [Pg.226]

Griffith, M., Huner, N. P. A., Espelie, K. E., Kolattukudy, P. E.. 1985. Lipid polymers accumulate in the epidermis and mestome sheath cell walls during low temperature development of winter rye leaves. Protoplasma 125 53-64. [Pg.974]

Trans-A -Hexadecenoic Acid, LHC II and Low Temperature Development in Herbaceous... [Pg.3841]

Improved bond strength in ceramic bodies is attained with mixtures of monoaluminum phosphate and colloidal silica when used with finely divided refractory powders of zircon, zirconia, or alumina (480). The reaction of P,0, with silica at relatively low temperature develops high bond strength in refractory compositions thus silica sol may be mixed with ammonium phosphate or other P,Os precursors at relatively low pH and used in minimal quantities as a binder in refractories (481,482). According to Lee, the binding properties of colloidal silica are improved by adding a soluble quaternary ammonium silicate such as tetramethylammonium silicate which is sufficiently alkaline to interact with the colloidal silica and cdhlesce it in a cement structure (483). [Pg.421]

Huner NPA, Krol M, Williams JP, Maissan E, Low PS, Roberts D. Thompson JE. Low Temperature Development Induces a Specific Decrease in trans-A -Hexadecenoic Acid Content which Influences LHCII Organization. Plant Physiol. 1987 84 12-18. [Pg.184]

An fuel-air mixture explosion can be initiated by a sudden discharge of static electricity. Yet, while flowing in systems, a fluid develops an electrical charge which will take as long to dissipate as the fluid is a poor conductor. The natural electrical conductivity of jet fuel is very low, on the order of a few picosiemens per meter, and it decreases further at low temperature. [Pg.251]

Several instniments have been developed for measuring kinetics at temperatures below that of liquid nitrogen [81]. Liquid helium cooled drift tubes and ion traps have been employed, but this apparatus is of limited use since most gases freeze at temperatures below about 80 K. Molecules can be maintained in the gas phase at low temperatures in a free jet expansion. The CRESU apparatus (acronym for the French translation of reaction kinetics at supersonic conditions) uses a Laval nozzle expansion to obtain temperatures of 8-160 K. The merged ion beam and molecular beam apparatus are described above. These teclmiques have provided important infonnation on reactions pertinent to interstellar-cloud chemistry as well as the temperature dependence of reactions in a regime not otherwise accessible. In particular, infonnation on ion-molecule collision rates as a ftmction of temperature has proven valuable m refining theoretical calculations. [Pg.813]

When considering how the evolution of life could have come about, the seeding of terrestrial life by extraterrestrial bacterial spores traveling through space (panspermia) deserves mention. Much is said about the possibility of some form of life on other planets, including Mars or more distant celestial bodies. Is it possible for some remnants of bacterial life, enclosed in a protective coat of rock dust, to have traveled enormous distances, staying dormant at the extremely low temperature of space and even surviving deadly radiation The spore may be neither alive nor completely dead, and even after billions of years it could have an infinitesimal chance to reach a planet where liquid water could restart its life. Is this science fiction or a real possibility We don t know. Around the turn of the twentieth century Svante Arrhenius (Nobel Prize in chemistry 1903) developed this theory in more detail. There was much recent excitement about claimed fossil bacterial remains in a Martian meteorite recovered from Antarctica (not since... [Pg.16]

E. Vedejs (1978) developed a general method for the sterically controlled electrophilic or-hydroxylation of enolates. This uses a bulky molybdenum(VI) peroxide complex, MoO(02)2(HMPTA)(Py), which is rather stable and can be stored below 0 °C. If this peroxide is added to the enolate in THF solution (base e.g. LDA) at low temperatures, oneO—O bond is broken, and a molybdyl ester is formed. Excess peroxide is quenched with sodium sulfite after the reaction has occurred, and the molybdyl ester is cleaved to give the a-hydroxy car-... [Pg.121]

The reaction is carried out at low temperature in aqueous medium and then allowed to stand overnight (221). Ammonium thiocarbamate is prepared from a cold saturated solution of ammonium thiocyanate, which is gradually added to dilute sulfuric acid at 25°C. The liberated carbonyl sulfide is passed into a saturated solution of alcoholic ammonia at about 10°C (221). The fairly low yield indicates that the reaction has not been greatly developed. [Pg.258]

Mobil has developed several 1L)P processes. In the 1970s, Mobil developed their LTD (Low Temperature Disproportionation) process (60,61). [Pg.416]

Nitrile mbber finds broad application in industry because of its excellent resistance to oil and chemicals, its good flexibility at low temperatures, high abrasion and heat resistance (up to 120°C), and good mechanical properties. Nitrile mbber consists of butadiene—acrylonitrile copolymers with an acrylonitrile content ranging from 15 to 45% (see Elastomers, SYNTHETIC, NITRILE RUBBER). In addition to the traditional applications of nitrile mbber for hoses, gaskets, seals, and oil well equipment, new applications have emerged with the development of nitrile mbber blends with poly(vinyl chloride) (PVC). These blends combine the chemical resistance and low temperature flexibility characteristics of nitrile mbber with the stability and ozone resistance of PVC. This has greatly expanded the use of nitrile mbber in outdoor applications for hoses, belts, and cable jackets, where ozone resistance is necessary. [Pg.186]

Sasol produces synthetic fuels and chemicals from coal-derived synthesis gas. Two significant variations of this technology have been commercialized, and new process variations are continually under development. Sasol One used both the fixed-bed (Arge) process, operated at about 240°C, as weU as a circulating fluidized-bed (Synthol) system operating at 340°C. Each ET reactor type has a characteristic product distribution that includes coproducts isolated for use in the chemical industry. Paraffin wax is one of the principal coproducts of the low temperature Arge process. Alcohols, ketones, and lower paraffins are among the valuable coproducts obtained from the Synthol process. [Pg.164]

However, BASF developed a two-step process (25). After methyl formate [107-31-3] became available in satisfactory yields at high pressure and low temperatures, its conversion to formamide by reaction with ammonia gave a product of improved quaUty and yield in comparison with the earlier direct synthesis. [Pg.508]


See other pages where Low-temperature developers is mentioned: [Pg.167]    [Pg.46]    [Pg.225]    [Pg.386]    [Pg.18]    [Pg.1569]    [Pg.3089]    [Pg.110]    [Pg.167]    [Pg.46]    [Pg.225]    [Pg.386]    [Pg.18]    [Pg.1569]    [Pg.3089]    [Pg.110]    [Pg.634]    [Pg.373]    [Pg.1437]    [Pg.215]    [Pg.76]    [Pg.142]    [Pg.60]    [Pg.219]    [Pg.312]    [Pg.239]    [Pg.250]    [Pg.252]    [Pg.392]    [Pg.255]    [Pg.406]    [Pg.38]    [Pg.134]    [Pg.478]    [Pg.304]    [Pg.556]   


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