Chromium efficiency

Electrophilic activation of coordinated peroxides can be achieved by protonation, which typically yields end-on coordinated hydroperoxides.16 For example, the well-defined hydroperoxo complexes of rhodium and chromium efficiently oxidize inorganic substrates such as halide anions these reactions are acid catalyzed.16 Hydroperoxo intermediates were implicated in some enzymatic oxidations, such as hydroxylation catalyzed by cytochrome P450 (Figure 4.32). Although significant... 

The low current efficiency of this process results from the evolution of hydrogen at the cathode. This occurs because the hydrogen deposition overvoltage on chromium is significantly more positive than that at which chromous ion deposition would be expected to commence. Hydrogen evolution at the cathode surface also increases the pH of the catholyte beyond 4, which may result in the precipitation of Cr(OH)2 and Cr(OH)2, causing a partial passivation of the cathode and a reduction in current efficiency. The latter is also inherently low, as six electrons are required to reduce hexavalent ions to chromium metal. 

The suitability of gas absorption as a pollution control method is generally dependent on the following factors 1) availability of suitable solvent 2) required removal efficiency 3) pollutant concentration in the inlet vapor 4) capacity required for handling waste gas and, 5) recovery value of the pollutant(s) or the disposal cost of the unrecoverable solvent. Packed-bed scrubbers are typically used in the chemical, aluminum, coke and ferro-alloy, food and agriculture, and chromium electroplating industries. 

For metal compounds, the calculation of the reportable concentration and treatment efficiency is based on the weight ot the parent metal, not on the weight of the metal compounds Metals are not destroyed, only physically removed or chemically converted from one form into another. The treatment efficiency reported represents only physical removal of the parent metal from the wastestream, not the percent chemical conversion of the metal compound. If a listed treatment method converts but does not remove a metal (e.g., chromium reduction), the method must be reported, but the treatment efficiency must be reported as zero. 

Precipitation is often applied to the removal of most metals from wastewater including zinc, cadmium, chromium, copper, fluoride, lead, manganese, and mercury. Also, certain anionic species can be removed by precipitation, such as phosphate, sulfate, and fluoride. Note that in some cases, organic compounds may form organometallic complexes with metals, which could inhibit precipitation. Cyanide and other ions in the wastewater may also complex with metals, making treatment by precipitation less efficient. A cutaway view of a rapid sand filter that is most often used in a municipal treatment plant is illustrated in Figure 4. The design features of this filter have been relied upon for more than 60 years in municipal applications. 

If homolytic reaction conditions (heat and nonpolar solvents) can be avoided and if the reaction is conducted in the presence of a weak base, lead tetraacetate is an efficient oxidant for the conversion of primary and secondary alcohols to aldehydes and ketones. The yield of product is in many cases better than that obtained by oxidation with chromium trioxide. The reaction in pyridine is moderately slow the intial red pyridine complex turns to a yellow solution as the reaction progresses, the color change thus serving as an indicator. The method is surprisingly mild and free of side reactions. Thus 17a-ethinyl-17jS-hydroxy steroids are not attacked and 5a-hydroxy-3-ket-ones are not dehydrated. 

The immediate outcome of the Hantzsch synthesis is the dihydropyridine which requires a subsequent oxidation step to generate the pyridine core. Classically, this has been accomplished with nitric acid. Alternative reagents include oxygen, sodium nitrite, ferric nitrate/cupric nitrate, bromine/sodium acetate, chromium trioxide, sulfur, potassium permanganate, chloranil, DDQ, Pd/C and DBU. More recently, ceric ammonium nitrate (CAN) has been found to be an efficient reagent to carry out this transformation. When 100 was treated with 2 equivalents of CAN in aqueous acetone, the reaction to 101 was complete in 10 minutes at room temperature and in excellent yield. 

There are obviously situations which demand considerable over-design of a cathodic protection system, in particular where regular and efficient maintenance of anodes is not practical, or where temporary failure of the system could cause costly damage to plant or product. Furthermore, contamination of potable waters by chromium-containing or lead-based alloy anodes must lead to the choice of the more expensive, but more inert, precious metal-coated anodes. The choice of material is then not unusual in being one of economics coupled with practicability. 

Several high-efficiency hard chromium plating baths are now available commercially. A solution which does not contain fluoride, and does not therefore attack steel or aluminium, has been described by Schwartz . At 50 A/dm and 53°C the cathode efficiency is about 25%, enabling deposition to be carried out at the rate of I m/min, with a consequent substantial saving in power and time. The deposit is bright, and has a hardness of about 1 050 Hy. 

In 1983, Nozaki, Takai, Hiyama, and their coworkers disclosed that vinyl and aryl iodides or bromides are reduced with chromium(n) chloride, and that the resulting organochromium(in) species react smoothly with a host of aldehydes to give allylic or benzylic alcohols in excellent yields.6 As shown in Scheme 1, the chromium(n) chloride-mediated carbonyl addition can be conducted efficiently at... 

This reaction is subject to a number of errors (1) the hydriodic acid (from excess of iodide and acid) is readily oxidised by air, especially in the presence of chromium(III) salts, and (2) it is not instantaneous. It is accordingly best to pass a current of carbon dioxide through the reaction flask before and during the titration (a more convenient but less efficient method is to add some solid sodium hydrogencarbonate to the acid solution, and to keep the flask covered as much as possible), and to allow 5 minutes for its completion. 

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