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Copper moderator

Copper status effects on resistance to endotoxin-induced injuries because burn and trauma patients show moderate copper deficiency and high risk to sepsis, and copper deficient rats are sensitive to endotoxins causing sepsis (DiSilvestro et al. 1995)... [Pg.209]

DiSilvestro RA, Carlson GP. 1990. Effects of moderate copper deficiency on carbon tetrachloride-induced hepatotoxicity in rats. Society for Experimental Biology and Medicine 32-35. [Pg.158]

Figure 8. Radiographs of humeri from rats raised on either a control-normal (Mnjj CUjj), or a moderate-manganese, moderate-copper (Mnj Cu ), or a manganese-free (Mnj n diet for 12 months. Figure 8. Radiographs of humeri from rats raised on either a control-normal (Mnjj CUjj), or a moderate-manganese, moderate-copper (Mnj Cu ), or a manganese-free (Mnj n diet for 12 months.
Many variations of copper catalysts have been tested. Since bulk copper and copper shavings show the same reactions obtained with copper on low-area supports, it appears that the support usually contributes little. A number of references on various forms of copper that have been described are collected in Table IX. Included are some on moderated copper catalysts. As has been discussed by Margolis (i), a number of electronegative elements act as moderators for copper... [Pg.183]

Beryllium is added to copper to produce an alloy with greatly increased wear resistance it is used for current-carrying springs and non-sparking safety tools. It is also used as a neutron moderator and reflector in nuclear reactors. Much magnesium is used to prepare light nieial allo>s. other uses include the extraction of titanium (p. 370) and in the removal of oxygen and sulphur from steels calcium finds a similar use. [Pg.124]

In the first method a secondary acetylenic bromide is warmed in THF with an equivalent amount of copper(I) cyanide. We found that a small amount of anhydrous lithium bromide is necessary to effect solubilization of the copper cyanide. Primary acetylenic bromides, RCECCH Br, under these conditions afford mainly the acetylenic nitriles, RCsCCHjCsN (see Chapter VIII). The aqueous procedure for the allenic nitriles is more attractive, in our opinion, because only a catalytic amount of copper cyanide is required the reaction of the acetylenic bromide with the KClV.CuCN complex is faster than the reaction with KCN. Excellent yields of allenic nitriles can be obtained if the potassium cyanide is added at a moderate rate during the reaction. Excess of KCN has to be avoided, as it causes resinifi-cation of the allenic nitrile. In the case of propargyl bromide 1,1-substitution may also occur, but the propargyl cyanide immediately isomerizes under the influence of the potassium cyanide. [Pg.155]

High purity acetaldehyde is desirable for oxidation. The aldehyde is diluted with solvent to moderate oxidation and to permit safer operation. In the hquid take-off process, acetaldehyde is maintained at 30—40 wt % and when a vapor product is taken, no more than 6 wt % aldehyde is in the reactor solvent. A considerable recycle stream is returned to the oxidation reactor to increase selectivity. Recycle air, chiefly nitrogen, is added to the air introducted to the reactor at 4000—4500 times the reactor volume per hour. The customary catalyst is a mixture of three parts copper acetate to one part cobalt acetate by weight. Either salt alone is less effective than the mixture. Copper acetate may be as high as 2 wt % in the reaction solvent, but cobalt acetate ought not rise above 0.5 wt %. The reaction is carried out at 45—60°C under 100—300 kPa (15—44 psi). The reaction solvent is far above the boiling point of acetaldehyde, but the reaction is so fast that Httle escapes unoxidized. This temperature helps oxygen absorption, reduces acetaldehyde losses, and inhibits anhydride hydrolysis. [Pg.76]

Nickel and Cobalt. Often present with copper in sulfuric acid leach Hquors are nickel [7440-02-0] and cobalt [7440-48-4]. Extraction using an organophosphoric acid such as D2EHPA at a moderate (3 to 4) pH can readily take out the nickel and cobalt together, leaving the copper in the aqueous phase, but the cobalt—nickel separation is more difficult (274). In the case of chloride leach Hquors, separation of cobalt from nickel is inherently simpler because cobalt, unlike nickel, has a strong tendency to form anionic chloro-complexes. Thus cobalt can be separated by amine extractants, provided the chloride content of the aqueous phase is carefully controUed. A successhil example of this approach is the Falcon-bridge process developed in Norway (274). [Pg.81]

In addition, molybdenum has high resistance to a number of alloys of these metals and also to copper, gold, and silver. Among the molten metals that severely attack molybdenum are tin (at 1000°C), aluminum, nickel, iron, and cobalt. Molybdenum has moderately good resistance to molten zinc, but a molybdenum—30% tungsten alloy is practically completely resistant to molten zinc at temperatures up to 800°C. Molybdenum metal is substantially resistant to many types of molten glass and to most nonferrous slags. It is also resistant to hquid sulfur up to 440°C. [Pg.465]

Another set of nickel aHoys, which have a high chromium content, a moderate molybdenum content, and some copper, are the ILLIUM aHoys. These cast aHoys are wear and erosion resistant and highly resistant to corrosion by acids and alkaHes under both oxidizing and reducing conditions. [Pg.6]

Toluhydroquinone and methyl / fX butyUiydroquinone provide improved resin color retention 2,5-di-/-butyIhydroquinone also moderates the cure rate of the resin. Quaternary ammonium compounds, such as benzyl trimethyl ammonium hydroxide, are effective stabilizers in combination with hydroquinones and also produce beneficial improvements in color when promoted with cobalt octoate. Copper naphthenate is an active stabilizer at levels of 10 ppm at higher levels (150 ppm) it infiuences the cure rate. Tertiary butylcatechol (TBC) is a popular stabilizer used by fabricators to adjust room temperature gelation characteristics. [Pg.317]

Atomic- Vapor Laser Isotope-Separation. Although the technology has been around since the 1970s, laser isotope separation has only recently matured to the point of industrialization. In particular, laser isotope separation for the production of fuel and moderators for nuclear power generation is on the threshold of pilot-plant demonstrations in several countries. In the atomic vapor laser isotope-separation (AVLIS) process, vibrationaHy cooled U metal atoms are selectively ionized by means of a high power (1—2 kW) tunable copper vapor or dye laser operated at high (kHz) repetition rates (51,59,60). [Pg.322]

When catalysts are used in a highly exothermic reaction, an active phase may be diluted with an inert material to help dissipate heat and moderate the reaction. This technique is practiced in the commercial oxychlorination of ethylene to dichloroethane, where an alumina-supported copper haUde catalyst is mixed with a low surface area inert diluent. [Pg.195]

This reaction is favored by moderate temperatures (100—150°C), low pressures, and acidic solvents. High activity catalysts such as 5—10 wt % palladium on activated carbon or barium sulfate, high activity Raney nickel, or copper chromite (nonpromoted or promoted with barium) can be used. Palladium catalysts are recommended for the reduction of aromatic aldehydes, such as that of benzaldehyde to toluene. [Pg.200]

Ethyl chloride is handled and transported in pressure containers under conditions similar to those appHed to methyl chloride. In the presence of moisture, ethyl chloride can be moderately corrosive. Carbon steel is used predominantly for storage vessels and prolonged contact with copper should be avoided. [Pg.3]

To a good approximation, thermal conductivity at room temperature is linearly related to electrical conductivity through the Wiedemann-Eran2 rule. This relationship is dependent on temperature, however, because the temperature variations of the thermal and the electrical conductivities are not the same. At temperatures above room temperature, thermal conductivity of pure copper decreases more slowly than does electrical conductivity. Eor many copper alloys the thermal conductivity increases, whereas electrical conductivity decreases with temperature above ambient. The relationship at room temperature between thermal and electrical conductivity for moderate to high conductivity alloys is illustrated in Eigure 5. [Pg.222]

Eig. 5. The Wiedemann-Eran2 relationship at 20°C between electrical and thermal conductivities of copper alloys having moderate to high conductivities. [Pg.222]

Stress Relaxation. Copper alloys are used extensively in appHcations where they are subjected to moderately elevated temperatures while under load. An important example is the spring member for contacts in electrical and electronic coimectors. Critical to rehable performance is the maintenance of adequate contact force, or stabiUty, while in service. Excessive decrease in this force to below a minimum threshold value because of losses in spring property can lead to premature open-circuit failure (see Electrical connectors). [Pg.225]

Fatigue properties in bending are most appropriate for copper aHoys as these are often used as spring contact components in beUows and electrical switches and coimectors. These articles are usuaHy designed for acceptable service Hves at a moderate to high number of stress cycles. [Pg.226]

Phosphor—bron2e alloys contain Cu, Sn or Cu, Sn, Pb, and have a residual phosphoms concentration of a few hundredths to 1%. Nickel can be added to refine the grain stmcture and is claimed to disperse the lead phase. Copper—tin bearings have high water resistance, high hardness, and moderately high strength. [Pg.243]


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See also in sourсe #XX -- [ Pg.54 ]




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