Sample records for benzoylphenylhydroxylamine

  1. Extractive-photometric determination of niobium with N-benzoylphenylhydroxylamine and lumogallion in alloyed steels

    International Nuclear Information System (INIS)

    Patratij, Yu.V.; Pilipenko, A.T.


    An extractive-photometric method has been developed to determine niobium (5) present as a heteroligand complex with N-benzoylphenylhydroxylamine (BPH) and lumogallion in alloyed steels. The method is based on preliminary extraction of niobium in a complex with BPH from concentrated HCl and subsequent determination of niobium in a 5-n (with respect to HCl) solution with lumogallion added. Sensitivity of the method is 2.0 μg of niobium in 10 ml of extract. The method has been tested on standard steels specimens

  2. Behavior of the extraction of metallic ions in carbonate medium, using N-benzoylphenylhydroxylamine (BPHA) - benzene

    International Nuclear Information System (INIS)

    Cipriani, M.


    The possibility of separating quantitatively trace impurities like Cu, Fe, In and Pb, present in uranium base materials of nuclear grade, is demonstrated. A solvent extraction is employed which makes use of -benzoylphenylhydroxylamine(BPHA)-benzene solution and separation is effected in a medium containing 252 moles per liter of sodium-uranyl tricarbonate at pH of 9,0. Carbonate ions under such conditions inhibit uranium extraction by masking uranyl ion-BPHA reaction. The uranyl ions show a demasking action, releasing, thereby, Pb(II) ions which are being extracted from carbonate medium. The Atomic Absorption Spectrophometry technique is used to obtain the experimental data [pt

  3. Solid-phase extraction of plutonium in various oxidation states from simulated groundwater using N-benzoylphenylhydroxylamine

    International Nuclear Information System (INIS)

    Perevalov, S.A.; Malofeeva, G.I.; Kuzovkina, E.V.; Spivakov, B.Ya.


    Solid-phase extraction of plutonium in different individual and mixed oxidation states from simulated groundwater (pH 8.5) was studied. The extraction of plutonium species was carried out in a dynamic mode using DIAPAK C16 cartridges modified by N-benzoylphenylhydroxylamine (BPHA). It was shown that the extent of recovery depends on the oxidation state of plutonium. The extraction of Pu(IV) was at the level of 98-99% regardless of the volume and flow-rate of the sample solution. Pu(V) was extracted by 90-95% and 75-80% from 10- and 100-mL aliquots of the samples, respectively, whereas the extraction of Pu(VI) did not exceed 45-50%. An equimolar mixture of Pu(IV), Pu(V), and Pu(VI) was extracted by 74%. The distribution coefficients (K d ) and kinetic exchange capacities (S) of plutonium in various oxidation states were measured. It was found that during the sorption process, Pu(V) was reduced to Pu(IV) by 80-90% after an hour-long contact with the solid phase. Pu(VI) is reduced to Pu(V) by 34% and to Pu(IV) by 55%. In the case of mixed-valent solution of plutonium, only Pu(V) and Pu(IV) were found in the effluents. (author)

  4. Uranium fluorides analysis. Titanium spectrophotometric determination

    International Nuclear Information System (INIS)


    Titanium determination in uranium hexafluoride in the range 0.7 to 100 microgrammes after transformation of uranium fluoride in sulfate. Titanium is separated by extraction with N-benzoylphenylhydroxylamine, reextracted by hydrochloric-hydrofluoric acid. The complex titanium-N-benzoylphenylhydroxylamine is extracted by chloroform. Spectrophotometric determination at 400 nm [fr

  5. Air pollution test methods

    Energy Technology Data Exchange (ETDEWEB)

    Yoneyama, E; Sugano, S; Fukui, S


    Vanadium exists in heavy oil as a chelate with mesoporphiline methyl ester, and the combustion ash of the oil may contain up to 80 percent of its oxides. Air is sampled in a standard way and to each 50 ml of the sample and blank solutions, add 5 ml of phosphoric acid and 2 ml of 10 percent ammonium sulfamate solution. After 10 min, the solution is titrated with potassium permanganate until it becomes purple. Two ml of hydrochloric acid and 10 ml of N-benzoylphenylhydroxylamine benzene solution are added and shaken for 30 sec. The benzene layer is washed with several portions of 2 ml HCl until no coloration of the HCl solution is visible. The benzene layer is transferred to a colorimetric tube and dried with granular calcium chloride. The absorbance is measured near 530 nm and the concentration is determined from a calibration curve previously prepared.