Simultaneous production of96Tc and111In by α-particle irradiation of stacked Nb and Ag foils,and their carrier-free separations

In order to produce routinely carrier-free⁹⁶Tc and¹¹¹In, their simultaneous production was examined by means of the stacked foil method. Both niobium and silver foils were arranged on the target holder so as the desired nuclear reactions took place effectively. Simultaneous irradiation of the target with 35 MeV -particles produced effectively¹¹¹In and⁹⁶Tc by the¹⁰⁹Ag(, 2n)¹¹¹In and⁹³Nb(, n)⁹⁶Tc reactions, respectively. Sufficient amounts of radioactivities for tracer uses are obtained by the irradiation at 5 A current for 2 hrs. In addition, carrier-free⁹⁶TcO₄ ^– in a perchloric acid solution could be prepared by the combined use of precipitation and anion-exchange methods. Separation of carrier-free¹¹¹In from the silver matrix was done by means of solvent extraction using acetylacetone as a chelating agent.     

Determination of carbon in copper by photon activation analysis

Determination of carbon in copper has been studied by photon activation analysis using 30 MeV bremsstrahlung. Chemical separation of carbon as CO₂ was performed by the combustion method in a high flow rate of oxygen stream. It has been demonstrated that the trace amount of carbon in copper can be determined accurately and precisely, and that the detection limit is 0.02 g.     

Kinetics of the phosphorescent triplet states of tetracyanobenzene complexes as studied by microwave induced delayed phosphorescence

Using microwave induced delayed phosphorescence techniques we determined the populating and depopulating rate constants for the individual spin-sublevels of the phosphorescent states of tetracyanobenzene (TCNB) and its charge-transfer complexes with benzene and hexamethylbenzene (HMB) in n-hexane at 1.25 K. It was shown that the non-radiative decay process from the shortest lifetime sublevel is most responsible for the previously observed shortening in the phosphorescence lifetime of the TCNBHMB complex.     

Delayed charge-transfer fluorescence of the tetracyanobenzene-biphenyl complex in the crystalline state

Intermolecular charge-transfer phosphorescence and fluorescence were observed for the biphenyl single crystal containing 1, 2, 4, 5-tetracyanobenzene as a guest. In addition, the delayed charge-transfer fluorescence due to triplet-triplet annihilation was observed for the first time.     

Angle-resolved photoemission of the c(2 × 2) and c(3 × 1) oxygen overlayers on Fe(110)

Angle-resolved photoemission spectroscopy utilizing synchrotron radiation has been used to study the band structure of the c(2×2) and (3×1) oxygen overlayers on Fe(110). The symmetries of the O-2p-derived states at the center of the surface Brillouin zone $\text{(}\text{Γ}\text{)}$ were identified using polarized light. At $\text{Γ}$ the p_xp_y- and p_z-derived levels are at about 5.5 and 7.0 eV below the Fermi level, respectively, for both ordered overlayers. The p-states of the c(2×2)-O structure show very little dispersion (?0.1 eV) with $\text{k}{}_{\mathrm{}}$. On the other hand, the c(3×1)-O overlayer exhibits considerable dispersion of ～1.6 eV. The essential features of the measured dispersion are reproduced well by the dispersion predicted in a qualitative way for an isolated c(3×1) oxygen monolayer.     

Electron spin resonance of phosphorescent triplet molecules observation of the proton hyperfine structure of Δm = ±2 transitions in stretched poly (vinyl alcohol) films

By applying a microwave magnetic field parallel to an external magnetic field, ESR of naphthalene, quinoxaline, quinoline and isoquinoline in their phosphorescent triplet states has been studied at 77 K. The proton hyperfine structures in the Δm = ± 2 transitions were distinctly resolved, especially when the stretched film was used as a host, compared with observations in ethanol glasses. The assignment of these ESR signals was carried out with the aid of the stretched-film method.     

Splittings of the octupole strength in Te isotopes

In the (p,p′) reaction on ¹³⁰Te, strong excitation of the second 3^? state was found at 3.36±0.01 MeV excitation energy. No strong second 3^? state was observed in the (p,p′) reaction on ¹²⁶Te.     

Determination of nitrate in natural waters by flow-injection analysis

Summary Nitrate was determined in natural water samples by flow-injection spectrophotometry. It was reduced to nitrite with copperized cadmium and the nitrite thus produced reacted with p-aminoacetophenone and m-phenylenediamine. The limit of detection was about 1.5 g l^–1 for sample injections of 650 l. The sampling rate was about 40 samples h^–1 and the relative standard deviation was above 1% for 0.1–0.3 mg l^–1 nitratenitrogen. Nitrite present in the sample was determined separately and subtracted.

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Nitratbestimmung in natürlichen Wässern mit Hilfe der Fließinjektions-Analyse

Zusammenfassung Nitrat wird bei dieser Methode mit Hilfe einer Cu/Cd-Reduktionssäule zu Nitrit reduziert, das mit p-Aminoacetophenon und m-Phenylendiamin zur Reaktion gebracht wird. Die gebildete Verbindung wird spektral-photometrisch gemessen. Die Nachweisgrenze beträgt etwa 1,5 g/l bei injizierten Probevolumina von 650 l. Der Probendurchsatz beträgt 40/h. Die relative Standardabweichung liegt über 1% bei 0,1–0,3 mg/l Nitrat-Stickstoff. Vorhandenes Nitrit wird gesondert bestimmt und abgezogen.