Cupric applications

The composition of this alloy (54% nickel, 15% molybdenum, 15% chromium, 5% tungsten and 5% iron) is less susceptible to intergranular corrosion at welds. The presence of chromium in this alloy gives it better resistance to oxidizing conditions than the nickel/molybdenum alloy, particularly for durability in wet chlorine and concentrated hypochlorite solutions, and has many applications in chlorination processes. In cases in which hydrochloric and sulfuric acid solutions contain oxidizing agents such as ferric and cupric ions, it is better to use the nickel/molybdenum/ chromium alloy than the nickel/molybdenum alloy. 

Except for sensor applications, the intercalation of alkali metal ions in metal hexacyanoferrates was used for adsorption and separation of cesium ions from different aqueous solutions with Prussian blue [43,44] and cupric hexacyanoferrate [45,46],... 

Nitric oxide (NO) and nitrite were found to be oxidized by Prussian blue and indium hexacyanoferrate-modified electrodes [75-77], For pharmaceutical application oxidation of isoprenaline [78] and vitamin B-6 [79] at cupric hexacyanoferrate-modified electrodes was shown. 

J. Wang and A.S. Arribas, Biocatalytically induced formation of cupric ferrocyanide nanoparticles and their application for electrochemical and optical biosensing of glucose. Small 2, 129 (2006). 

The oxidation of ethylene to acetaldehyde by dioxygen catalyzed by palladium and cupric salts found important technological application. The systematic study of this process was started by Smidt [245] and Moiseev [246]. The process includes the following stoichiometric stages [247,248] ... 

Aliphatic and aromatic sulfides undergo desulfurization with Raney nickel [673], with nickel boride [673], with lithium aluminum hydride in the presence of cupric chloride [675], with titanium dichloride [676], and with triethyl phosphite [677]. In saccharides benzylthioethers were not desulfurized but reduced to toluene and mercaptodeoxysugars using sodium in liquid ammonia [678]. This reduction has general application and replaces catalytic hydrogenolysis, which cannot be used [637]. 

An alternate procedure used in a few specialty applications is the cuprammonium process. This involves stabilization of cellulose in an ammonia solution of cupric oxide. Solubilization occurs by complex formation of cupric ion with ammonia and the hydroxyl groups of cellulose. Regeneration of cellulose, after formation of the desired products, is accomplished by treatment with acid. The main application of the cuprammonium process is for the synthesis of films and hollow fibers for use in artificial kidney dialysis machines. The cuprammonium process yields products with superior permeability and biocompatibility properties compared to the xanthation process. Less than 1% of all regenerated cellulose is produced by the cuprammonium process. 

The applications of cupric ferrocyanide are very limited. It is used as a chemical membrane for osmosis. 

Colorimetric Methods. Numerous colorimetric methods exist for the quantitative determination of carbohydrates as a group (8). Among the most popular of these is the phenol—sulfuric acid method of Dubois (9), which relies on the color formed when a carbohydrate reacts with phenol in the presence of hot sulfuric acid. The test is sensitive for virtually all classes of carbohydrates. Colorimetric methods are usually employed when a very small concentration of carbohydrate is present, and are often used in clinical situations. The Somogyi method, of which there are many variations, relies on the reduction of cupric sulfate to cuprous oxide and is applicable to reducing sugars. 

Application 2.—The second plan of procedure is well illustrated in the preparation of cupric chloride, which is very soluble in water. The cheapest salt of copper is the sulfate, and this may be brought into double... 

Fig. 4.26 Discharge curve of a lithium-cupric sulphide pacemaker cell al 37°C under a load of 12.3 kfi. (By permission of the Electrochemical Society A.J, Cuesta and D.D. Bump, Proceedings of the symposia on power sources for biomedical implantable applications and ambient temperature lithium batteries, eds B.B. Owens and N. Margalil, 1980. p. 95.)...

Di(3-benzo[6]thienyl)methane is obtained by treatment of 3-benzo-[6]thienylmagnesium bromide with 3-chloromethylbenzo [ thiophene.486 Two molecules of 3-benzo[6]thienylmagnesium iodide may be coupled by treatment with cupric chloride,305 but not with cupric bromide or nickel bromide,349 to yield 3,3 -di(benzo[6]thienyl). A claim349 to have prepared the same compound by the Ullmann reaction is probably not justified.305 The Ullmann reaction otherwise seems to be of general application in the benzo [6]thiophene series.87-483 Halobenzo[6]thiophenes76 105 511 can be selectively metallated in the 2-position by the use of w-butyllithium (Section VII). 

The cyclopropanation of alkenes, alkynes, and aromatic compounds by carbenoids generated in the metal-catalyzed decomposition of diazo ketones has found widespread use as a method for carbon-carbon bond construction for many years, and intramolecular applications of these reactions have provided a useful cyclization strategy. Historically, copper metal, cuprous chloride, cupric sulfate, and other copper salts were used most commonly as catalysts for such reactions however, the superior catalytic activity of rhodium(ll) acetate dimer has recently become well-established.3 This commercially available rhodium salt exhibits high catalytic activity for the decomposition of diazo ketones even at very low catalyst substrate ratios (< 1%) and is less capricious than the old copper catalysts. We recommend the use of rhodium(ll) acetate dimer in preference to copper catalysts in all diazo ketone decomposition reactions. The present synthesis describes a typical cyclization procedure. 

HPhe Fricke dosimeter (ferrous sulfate solutions) has been used to measure A the radiation intensity of various types of ionizing radiation sources since its development by Fricke and Morse in 1927 (2). It is widely accepted because it yields accurate and reproducible results with a minimum of care. This system meets many of the requirements specified for an ideal dosimeter (5, 9) however, it has a limited dose range, and for our applications it has been necessary to develop a dosimeter covering larger doses. Of the systems reviewed (6, 7), two (ferrous sulfate-cupric sulfate and ceric sulfate) showed the most promise for use with the radiation sources at the U. S. Army Natick Laboratories (8). Of these, the ferrous-cupric system has received the most use, and this paper describes our experience in using this system and suggests procedures by which it may be used by others with equal success. 

The cycle approach for oxidation has been adopted at an industrial level for the Wacker-Chemie process for acetaldehyde production, in which ethylene is first put in contact with the oxidized catalyst solution, containing palladium chloride, and in the second step the solution containing the reduced catalyst is sent to a regeneration reactor containing cupric chloride and inside which also air is fed. The regenerated catalyst solution is returned to the first oxidation stage. Another industrial application is the Lummus process for the anaerobic ammoxidation of o-xylene to o-phthaloni-trile [68]. Du Pont has developed the oxidation of n-butane to maleic anhydride catalyzed by V/P/O, in a CFBR reactor, and built a demonstration unit in Spain [69] however, a few years ago the plant was shut down, due to the bad economics. 

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