Oxalic copper oxalate

Caswell No. 248A Copper oxalate Copper oxalate (CUC2O4) Copper(ll) oxalate Crow Chex Cupric oxalate EINECS 212-411-4 EPA PesWde Chemical Code 023305 Ethanedioic acid copper salt Ethanedioic acid, copper(2+) salt (1 1) HSDB 265 NSC 112246... 

Oxalic acid produced from syngas can be esteiified (eq. 20) and reduced with hydrogen to form ethylene glycol with recovery of the esterification alcohol (eq. 21). Hydrogenation requires a copper catalyst giving 100% conversion with selectivities to ethylene glycol of 95% (15). 

Resorcinol or hydroquinone production from m- or -diisopropylben2ene [100-18-5] is realized in two steps, air oxidation and cleavage, as shown above. Air oxidation to obtain the dihydroperoxide (DHP) coproduces the corresponding hydroxyhydroperoxide (HHP) and dicarbinol (DC). This formation of alcohols is inherent to the autooxidation process itself and the amounts increase as DIPB conversion increases. Generally, this oxidation is carried out at 90—100°C in aqueous sodium hydroxide with eventually, in addition, organic bases (pyridine, imidazole, citrate, or oxalate) (8) as well as cobalt or copper salts (9). 

In acidic solution, the degradation results in the formation of furfural, furfuryl alcohol, 2-furoic acid, 3-hydroxyfurfural, furoin, 2-methyl-3,8-dihydroxychroman, ethylglyoxal, and several condensation products (36). Many metals, especially copper, cataly2e the oxidation of L-ascorbic acid. Oxalic acid and copper form a chelate complex which prevents the ascorbic acid-copper-complex formation and therefore oxalic acid inhibits effectively the oxidation of L-ascorbic acid. L-Ascorbic acid can also be stabilized with metaphosphoric acid, amino acids, 8-hydroxyquinoline, glycols, sugars, and trichloracetic acid (38). Another catalytic reaction which accounts for loss of L-ascorbic acid occurs with enzymes, eg, L-ascorbic acid oxidase, a copper protein-containing enzyme. 

Dimethyl carbonate [616-38-6] and dimethyl oxalate [553-90-2] are both obtained from carbon monoxide, oxygen, and methanol at 363 K and 10 MPa (100 atm) or less. The choice of catalyst is critical cuprous chloride (66) gives the carbonate (eq. 20) a palladium chloride—copper chloride mixture (67,68) gives the oxalate, (eq. 21). Anhydrous conditions should be maintained by removing product water to minimize the formation of by-product carbon dioxide. 

Many reactions catalyzed by the addition of simple metal ions involve chelation of the metal. The familiar autocatalysis of the oxidation of oxalate by permanganate results from the chelation of the oxalate and Mn (III) from the permanganate. Oxidation of ascorbic acid [50-81-7] C HgO, is catalyzed by copper (12). The stabilization of preparations containing ascorbic acid by the addition of a chelant appears to be negative catalysis of the oxidation but results from the sequestration of the copper. Many such inhibitions are the result of sequestration. Catalysis by chelation of metal ions with a reactant is usually accomphshed by polarization of the molecule, faciUtation of electron transfer by the metal, or orientation of reactants. 

The pH effect in chelation is utilized to Hberate metals from thein chelates that have participated in another stage of a process, so that the metal or chelant or both can be separately recovered. Hydrogen ion at low pH displaces copper, eg, which is recovered from the acid bath by electrolysis while the hydrogen form of the chelant is recycled (43). Precipitation of the displaced metal by anions such as oxalate as the pH is lowered (Fig. 4) is utilized in separations of rare earths. Metals can also be displaced as insoluble salts or hydroxides in high pH domains where the pM that can be maintained by the chelate is less than that allowed by the insoluble species (Fig. 3). 

The reactor has been successfully used in the case of forced precipitation of copper and calcium oxalates (Jongen etal., 1996 Vacassy etal., 1998 Donnet etal., 1999), calcium carbonate (Vacassy etal., 1998) and mixed yttrium-barium oxalates (Jongen etal., 1999). This process is also well adapted for studying the effects of the mixing conditions on the chemical selectivity in precipitation (Donnet etal., 2000). When using forced precipitation, the mixing step is of key importance (Schenk etal., 2001), since it affects the initial supersaturation level and hence the nucleation kinetics. A typical micromixer is shown in Figure 8.35. 

Cupri-. cupric, copper(II). -azetst, n. cupric acetate, copper(II) acetate, -carbonat, n. cupric carbonate, copper(II) carbonate, -chlorid, n. cupric chloride, copper(II) chloride. -hydroxyd, n. cupric hydroxide, cop-per(II) hydroxide. -ion, n. cupric ion, copper(II) ion. -ozalat, n. cupric oxalate, copper(II) oxalate, -oxyd, n. cupric oxide, copper(II) oxide. -salz, n. cupric salt, copper(II) salt, -suifat, n. cupric sulfate. copper(II) sulfate, -sulfid, n. cupric sulfide, copper(II) sulfide, -verbihdung, /. cupric compound, copper(II) compound, -wein-saure, /. cupritartaric acid. 

Molybdenum tends to be protected by vanadium in aerated 7 1 % hydrochloric acid and it receives a high degree of protection when coupled with copper in this medium. Molybdenum corrodes somewhat faster than normal in 3 1 % nitric acid when coupled with tungsten. It is not affected by contact with titanium in 3-1% nitric acid. It is protected by aluminium and copper in aerated 10% formic acid and by aluminium in air-aerated 9% oxalic acid. In the latter solution, copper had only a slight protective effect when coupled with molybdenum. 

Appreciable errors may also be introduced by post-precipitation. This is the precipitation which occurs on the surface of the first precipitate after its formation. It occurs with sparingly soluble substances which form supersaturated solutions they usually have an ion in common with the primary precipitate. Thus in the precipitation of calcium as oxalate in the presence of magnesium, magnesium oxalate separates out gradually upon the calcium oxalate the longer the precipitate is allowed to stand in contact with the solution, the greater is the error due to this cause. A similar effect is observed in the precipitation of copper or mercury(II) sulphide in 0.3M hydrochloric acid in the presence of zinc ions zinc sulphide is slowly post-precipitated. 

Before use, electrodes must be carefully cleaned to remove any previous deposits. Deposits of copper, silver, cadmium, mercury, and many other metals can be removed by immersion in dilute nitric acid (1 1), rinsing with water, then boiling with fresh 1 1 nitric acid for 5-10 minutes, followed by a final washing with water. Deposits of lead dioxide are best removed by means of 1 1 nitric acid containing a little hydrogen peroxide to reduce the lead to the Pb(II) condition ethanol or oxalic acid may replace the hydrogen peroxide. 

Sulphuric acid is not recommended, because sulphate ions have a certain tendency to form complexes with iron(III) ions. Silver, copper, nickel, cobalt, titanium, uranium, molybdenum, mercury (>lgL-1), zinc, cadmium, and bismuth interfere. Mercury(I) and tin(II) salts, if present, should be converted into the mercury(II) and tin(IV) salts, otherwise the colour is destroyed. Phosphates, arsenates, fluorides, oxalates, and tartrates interfere, since they form fairly stable complexes with iron(III) ions the influence of phosphates and arsenates is reduced by the presence of a comparatively high concentration of acid. 

A. niger normally produces many useful secondary metabolites citric and oxalic acids are stated as the dominant products. Limitation of phosphate and certain metals such as copper, iron and manganese results in a predominant yield of citric acid. The additional iron may act as a cofactor for an enzyme that uses citric acid as a substrate in the TCA cycle as a result, intermediates of the TCA cycle are formed. 

Lassaletta et al. designed new hgands for the copper-catalyzed Diels-Alder reaction by introduction of C2-symmetric dialkylamino substructures in gly-oxal bis-hydrazones [104] (73 in Scheme 40). This hgand can advantageously be prepared in its both enantiomeric forms on a multigram scale from 1,4-diphenylbutanedione. 

Copper is a component of the oxalate decarboxylase in Bacillus subtilis that converts oxalate into formate and CO2 (Tanner et al. 2001). 

Urea was treated with oxalic acid and carbon. The operation was carried out in the presence of anhydrous copper sulphate in order to detect the water formed, and gases were expected to bubble through a barium hydroxide solution to be able to see carbon dioxide. Unfortunately, the apparatus was closed by mistake. It detonated due to the large quantity of gases formed in the reaction ... 

A PRP -1 (Hamilton Reno, NV) reversed phase column was coated with cetylpyridinium and eluted with tetramethylammonium salicylate acetoni-trile water.89 The separation was comparable to that observed on conventional ion exchange. Coated phases were also used to separate oxalate complexes of manganese, cobalt, copper, and zinc.90 Reversed phase silica supports were coated with poly(N-ethyl-4-vinylpyridinium bromide), poly(dimethydiallylammonium chloride), poly(hexamethyleneguanidinium... 

In the presence of soluble cations (e.g. Fe, Cu), additions of small quantities of organic acid (e.g. oxalic, tartaric) improve gold recovery in the copper concentrate. 

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