Gerasimenko, G.I.; Tishchenko, M.A.; Poluehktov, N.S.
Spectrometry has been used for studying the formation of different-ligand complexes of Nd 3+ , Ho 3+ , and Er 3+ with diantipyrylmethane (DAM) and gallic aicd (GA) at pH 10.0-12.0. It has been found that in the complex being formed one ion of rare earth element interacts with one molecule of DAM and three molecules of GA. The oscillator forces grow when passing from aquaions to compounds with gallic acid and then with DAM and GA. The oscillator forces of Nd 3+ and Er 3+ depend linearly on those of Ho 3+ in the solutions of complexes with DAM and GA
Tishchenko, M A; Gerasimenko, G I; Poluehktov, N S [AN Ukrainskoj SSR, Odessa. Inst. Obshchej i Neorganicheskoj Khimii
To elucidate the possibility of using pyrazolone-5-diantipyril-methane (DAM) derivative for determination of terbium microimpurities, the conditions have been studied of luminescent determination of terbium in complex compounds containing an ion of rare-earth element, diantipyrilmethane, and salicylic acid (Sal.). The ratio between the components in the complex REE-DAM-Sal is 1:1:3. La, Y, Gd do not affect the luminescence intensity of terbium complex. A luminescent method of determining terbium traces in highly pure oxides of lanthanum, gadolinium, lutetium, and yttrium has been developed in which suspensions of complex precipitation are used. The amount of terbium determined in oxide of lanthanum, gadolinium, and lutetium is (1-5)x10/sup -6/% and (2-3)x10/sup -5/% in yttrium oxide.
Ganago, L I; Alinovskaya, L A [AN Belorusskoj SSR, Minsk. Inst. Fiziki Tverdogo Tela i Poluprovodnikov
The reactions of scandium with homologs of diantipyrilmethane (DAM)-propyldiantipyrilmethane (PDAM) and phenyldiantipyrilmethane (PhDAM) - are studied. The relationship of components in the complexes formed is found, and chemism of their formation is established. The complexes Sc-SPADNE (sodium salt 2-(n-sulphophenylazo)-1,8-dioxynaphthalene-3,6-disulphonic acid) are shown to form within a wide pH range. The maximum yield of complexes is observed at 6.0-7.5 pH. By the ion-exchange method the anion character of heteroligand scandium complexes is established. The complex Sc-SPADNE-PDAM is faster as compared with the complexes Sc-SPADNE-DAM and Sc-SPADNE-PhDAM. The decrease in amine excess and increase in the sensitivity of heteroligand formation of the complexes of scandium with SPADNE and PDAM make them better suited for analysis. The technique is developed for the determination of Sc/sub 2/O/sub 3/ in perovskites using the complete differential spectrophotometry method.
Ul' yanova, T M; Gerasimenko, G N; Tishchenko, M A; Vitkun, R A [AN Ukrainskoj SSR, Odessa. Fiziko-Khimicheskij Inst.
Using luminescence method different-ligand complexing of europium ions with diantipyrylalkanes and cyclic ..beta..-diketones: 2-acetyl- and 2-benzoyl-1.3-indandions, has been studied. The optimum conditions of the formation of different-ligand complexes and the ratio of components in it are determined. Effect of alien lanthanides and diantipyrylmethane derivatives on the luminescence intensity of europium complexes is clarified. A correlation between the ratio of the luminescence intensity bands of europium complexes and the values of oscillator strengths of supersensitive transitions of neodymium and erbium absorption bands is established.
An extraction system consisting of one aqueous and two organic phases is described. Diantipyrylmethane (DAM) is used as the extractant for bismuth and tellurium, which are extracted into the smaller of the two organic phases from nitric acid and perchloric acid respectively. The extraction efficiency is in the range of 90 to 95 per cent, compensation for incomplete extraction being made by the technique of standard addition. Copper, lead, and zinc are not extracted in either procedure. When the solutions contain high concentrations of iron, thioglycolic acid is used as a masking agent for iron in the extraction of bismuth. Atomic-absorption spectrophotometry is used for the analysis of the third phase after it has been diluted with methanol. The precision for bismuth and tellurium is in the range of 3 to 4 per cent. The accuracy, as ascertained from comparative analyses of sulphide concentrates, is good
A method for the systematic activation analysis of seven noble metals - ruthenium, silver, rhenium, osmium, iridium, platinum and gold - in rocks were developed and examined with radiotracers and irradiated rock samples. After the fusion of the irradiated rock sample with sodium hydroxide and sodium peroxide, 10% sodium sulfide solution is added and rhenium is extracted with pyridine-benzene mixture from 6N sodium hydroxide solution. From the hydroxide-sulfide precipitate fraction, ruthenium and osmium are distilled as tetroxides, silver is precipitated as chloride, gold is extracted with ethyl acetate, and iridium and platinum are extracted with diantipyrylmethane. Each fraction is purified and subjected to the γ-ray spectrometry. Chemical yields for the elements are more than 60%. Determination limits are given for the seven elements. (author)
Zheng Fengying; Li Shunxing; Lin Luxiu; Cheng Liqing
A novel method for preconcentration of Ti(IV) with nanometer size ZrO 2 and determination by spectrophotometry has been developed. Ti(IV) was selectively adsorbed on 300 mg ZrO 2 from 500 mL solution at pH 6.0, then eluted by 5 mL 11.3 mol L -1 HF. The eluent added was diantipyrylmethane (DAPM, as chromogenic reagent) and ascorbic acid (as masking agent), used for the analysis of Ti(IV) by measuring the absorbance at 390 nm with spectrophotometry, based on the chromogenic reaction between the Ti(IV) and DAPM. This method gave a concentration enhancement of 100 for 500 mL sample, eliminated the sizable interferences on direct determination with spectrophotometry. Detection limit (3σ, n = 11) of 0.1 μg L -1 was obtained. The method was applied to determine the concentration of Ti(IV) in river water and seawater and the analytical recoveries of Ti(IV) added to samples were 97.6-101.3%.