Cobalt detection

Water content No decanted water Non-detectable by cobalt bromide test (NF M 41-004) Pass valve freezing test (ASTM D 2713, ISO 13758)... 

Hydantoin itself can be detected ia small concentrations ia the presence of other NH-containing compounds by paper chromatography followed by detection with a mercury acetate—diphenylcarba2one spray reagent. A variety of analytical reactions has been developed for 5,5-disubstituted hydantoias, due to their medicinal iaterest. These reactions are best exemplified by reference to the assays used for 5,5-diphenylhydantoiQ (73—78), most of which are based on their cycHc ureide stmcture. Identity tests iaclude the foUowiag (/) the Zwikker reaction, consisting of the formation of a colored complex on treatment with cobalt(II) salts ia the presence of an amine (2) formation of colored copper complexes and (3) precipitation on addition of silver(I) species, due to formation of iasoluble salts at N. ... 

Analysis of zinc solutions at the purification stage before electrolysis is critical and several metals present in low concentrations are monitored carefully. Methods vary from plant to plant but are highly specific and usually capable of detecting 0.1 ppm or less. Colorimetric process-control methods are used for cobalt, antimony, and germanium, turbidimetric methods for cadmium and copper. Alternatively, cadmium, cobalt, and copper are determined polarographicaHy, arsenic and antimony by a modified Gutzeit test, and nickel with a dimethylglyoxime spot test. 

The detection and determination of traces of cobalt is of concern in such diverse areas as soflds, plants, fertilizers (qv), stainless and other steels for nuclear energy equipment (see Steel), high purity fissile materials (U, Th), refractory metals (Ta, Nb, Mo, and W), and semiconductors (qv). Useful techniques are spectrophotometry, polarography, emission spectrography, flame photometry, x-ray fluorescence, activation analysis, tracers, and mass spectrography, chromatography, and ion exchange (19) (see Analytical TffiTHODS Spectroscopy, optical Trace and residue analysis). 

In this work ion-exchange and gel-permeation chromatography coupled with membrane filtration, photochemical oxidation of organic metal complexes and CL detection were applied to the study of the speciation of cobalt, copper, iron and vanadium in water from the Dnieper reservoirs and some rivers of Ukraine. The role of various groups of organic matters in the complexation of metals is established. 

In addition to the Raney nickel catalysts, Raney catalysts derived from iron, cobalt, and copper have been examined for their action on pyridine. At the boiling point of pyridine, degassed Raney iron gave only a very small yield of 2,2 -bipyridine but the activity of iron in this reaction is doubtful as the catalyst was subsequently found to contain 1.44% of nickel. Traces of 2,2 -bipyridine (detected spectroscopically) were formed from pyridine and a degassed, Raney cobalt catalyst but several Raney copper catalysts failed to produce detectable quantities of 2,2 -bipyridine following heating with pyridine. 

Chiral salen chromium and cobalt complexes have been shown by Jacobsen et al. to catalyze an enantioselective cycloaddition reaction of carbonyl compounds with dienes [22]. The cycloaddition reaction of different aldehydes 1 containing aromatic, aliphatic, and conjugated substituents with Danishefsky s diene 2a catalyzed by the chiral salen-chromium(III) complexes 14a,b proceeds in up to 98% yield and with moderate to high ee (Scheme 4.14). It was found that the presence of oven-dried powdered 4 A molecular sieves led to increased yield and enantioselectivity. The lowest ee (62% ee, catalyst 14b) was obtained for hexanal and the highest (93% ee, catalyst 14a) was obtained for cyclohexyl aldehyde. The mechanism of the cycloaddition reaction was investigated in terms of a traditional cycloaddition, or formation of the cycloaddition product via a Mukaiyama aldol-reaction path. In the presence of the chiral salen-chromium(III) catalyst system NMR spectroscopy of the crude reaction mixture of the reaction of benzaldehyde with Danishefsky s diene revealed the exclusive presence of the cycloaddition-pathway product. The Mukaiyama aldol condensation product was prepared independently and subjected to the conditions of the chiral salen-chromium(III)-catalyzed reactions. No detectable cycloaddition product could be observed. These results point towards a [2-i-4]-cydoaddition mechanism. 

Repeat the experiment in the presence of 500 jug of iron(III) and 500 jug of aluminium ions no interference will be detected, but cobalt may interfere (Note 2). 

The chiral cyclic cobalt enolate 2 reacts with acetone to produce the aldol adduct 3 which arises from attack of the electrophile from the least hindered side of the enolate, i.e., away from the phosphane13. None of the other possible diastereomers was detected. 

A particle size effect has been detected by Chou and Olson [486] in the isothermal decomposition of isothiocyanatopentammine cobalt(III) perchlorate. Below a = 0.09, the larger crystals decompose relatively more rapidly than the smaller, whereas for a > 0.09, the reverse is true. This behaviour was attributed to enhanced nucleation in the larger particles due to strain, but this favourable factor was later offset by the inhibiting influence of the product ammonia which accumulated in the larger crystals. 

Formazan, l-(2-hydroxy-5-suIfophenyl)-3-phenyl-5-(2-carboxyphenyl)-zinc detection, 6, 83 Formazans cobalt complexes dyes, 6, 81 metal complexes bidentate, 6, 78 color photography, 6,111 dyes, 6, 77 tetradentate, 6, 81 tridentate, 6, 79... 

Patil, V.a, Sevalkar, M.T.. Fidalikar, SV. "rhiii-layer Chiomatognphic Detection of Eo-doml n and Photphamidon by Use of Cobalt Acetate and o-lblidine , 1 C/mMnafdgr. 1990, 519. 268-270. 

The detection limits for iron and cobalt cations on cellulose layers are 2 and 20 ng substance per chromatogram zone [1]. 

Cobalt(II) ions (h/Jj 65-70) yielded pale blue and iron(III) ions (h/ f 85-90) red-brown chromatogram zones on a colorless background. The detection Umits per chromatogram zone were 2 ng for iron and 20 ng for cobalt. 

Further work on nickelocene and cobaltocene was done by Ross , who synthesized the respective compounds using Ni, Ni and " Co, which decay be E.C., jS and a fully converted isomeric transition, respectively, all producing radioactive cobalt isotopes. The results showed retentions, after sublimation, of 84%, 83% and 80%, respectively. The composition of the unsublimable residue was largely CoCp2, except for the highly converted "Co, where only 30% CoCpj could be detected. This was interpreted as showing that by internal conversion the molecules are totally destroyed, by the same sort of argument as was used by Riedel and Merz . 

This Study has shown that reasonably uniform platinum crystallites can be made on y-alumlna, and that platinum and palladium can be segregated and maintained In that form for the most part even after exposure to high temperature oxidation-reduction conditions. Highly dispersed clusters of palladium, nickel, cobalt, and Iron can be observed. Cluster size determination could not be accurately made because of the lack of contrast between the cluster and the support. The marginal detectability by EDS for these clusters enabled elemental Identification to be made, however, mass uniformity determinations could not be made. 

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