Selective actinide solvent extraction used in conjunction with liquid scintillation

New commercial liquid scintillation counters allow rapid / measurements. Associated with liquid-liquid extraction techniques, rapid and selective actinide analyses are possible. Uranium, thorium and americium extractions with tri-n-octylphosphine oxide (TOPO) in toluene have been investigated. Detection limits of 40 mBq·l^–1 for -emitters are currently obtained with a Packard 2550 TR/AB^TM liquid scintillation analyzer.     

Energy resolution of liquid scintillator for α-particles and internal conversion electrons at lower temperatures

The energy resolution of -particles from²⁴¹Am,²²²Rn,²¹⁸Po and²¹⁴Po and internal conversion electrons from^131mXe with a liquid scintillation system has been studied at temperatures from 13 °C to –65 °C. At lower temperatures the liquid scintillation system has shown to give better energy resolutions both for -particles and internal conversion electrons compared with the values obtained at ordinary temperature. The phenomena were explained by the increase in light output of liquid scintillator at lower temperatures.     

Gelation with N-lauroyl-L-glutamic-α,γ-dibutylamide for liquid scintillation counting of low specific activities of35S and32P

A gelling agent, N-lauroyl-L-glutamic-,-dibutylamide, was applied for liquid scintillation counting of inorganic³²P and³⁵S. The gel with toluene cocktail is transparent and rigid for a long time. Several grams of ammonium magnesium phosphate or barium sulfate can easily be measured without complicating procedures.     

Improvement for α-energy resolution in determination of low level plutonium by liquid scintillation counting

An improvement of -energy resolution for determining low level plutonium has been investigated using combined solvent extraction-low level liquid scintillation counter. In the present work, -energy resolution of 270–290 keV for liquid scintillation spectra of²³⁶Pu and²³⁹Pu is attained. Thus the simultaneous determination of low level plutonium with -liquid scintillation spectrometry may be practized.     

Recent progress and application of low level liquid scintillation counting

The use of an ultra low level liquid scintillation counter with extremely low background, MCA technique, storage and software evaluation of pulse height spectra has given very low LLD's, the possibility of - and -spectrometry to some extent and time saving optimization of counting conditions. Quick and very simple but yet accurate analytical methods could be worked out worked out for environmental measurements: Environmental levels of tritium,¹⁴C in several assimilation products,²²²Rn and²²⁶Ra in water without any sample pretreatment. Suggestions for possible further applications in environmenial monitoring and low level counting are given.     

Energy shift of vanadium Kα X-rays accompanying EC decay in51Cr-labeled compounds

The VK X-rays induced by the electron capture decay of⁵¹Cr-labeled compounds and the fluorescent X-rays of the vanadium compounds have been measured with a Bragg spectrometer. The evident chemical shifts of the K₁ and K₂ lines were observed for the oxidation state both by electron capture and photoionization. The differences of the K peak energy (K₁ and K₂ peaks) with the modes of the excitation were also obtained. The K peaks of⁵¹Cr shift to lower energy by ca. 0.5 eV than those of vanadium at the same oxidation state. This is because the probability of the electron shake up (and shake off) during the electron capture decay is extremely small, as compared to photoionization.     

Determination of 222Rn in Iranian mineral waters using liquid scintillation alpha-spectrometry

Liquid scintillation counting (LSC) method has been used for the measurement of ²²²Rn in mineral water samples under a pilot project for the first surveillance in Iran. Low level background LSC counter Quantulus and pulse-shape analysis method have been employed. The concentration of ²²²Rn found in mineral waters of the studied areas ranges from about 1 to 75 Bq/l. The best lower limit of detection obtained with the applied technique was 0.069 Bq/l for a counting time in the range of 236–296 minutes.     

Studies on the feasibility of production of57Co by alpha bombardment of Mn and Ni targets

We have studied the feasibility of producing⁵⁷Co (271.3 d) via the⁵⁵Mn(, 2n)⁵⁷Co reaction (⁵⁵Mn–100%). The thick target yield of⁵⁷Co in the 28 to 18 MeV energy region was measured as 3.87 Ci/Ah. However, the proximity and overlap of the excitation functions for (, n), (, 2n) and (, 3n) reactions on⁵⁵Mn are such that the production of pure⁵⁷Co in high yields free of⁵⁸Co (70.8 d) and⁵⁶Co (78.8 d) has not been feasible. We have also studied a new method for ancillary production of⁵⁷Co via the reactions⁵⁸Ni(, p)⁵⁷Co and during the course of producing⁶²Zn by⁶⁰Ni(, 2n)⁶²Zn reaction. In this case the yield of⁵⁷Co of reasonable purity has been up to 1 Ci/Ah.     

Regioselective synthesis of α- and α'-sulfur-containing ethyl esters of dehydrodesthiobiotin

Conclusions The ethyl esters of- and'-oxodehydrodesthiobiotin when reacted with thioacetic acid in the presence of BF₃ etherate respectively give the ethyl esters of-thiooxo- and, -diacetytmercaptodehydrodesthiobiotin.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 954–956, April, 1978.     

Complex polarizability as used to analyze dielectric relaxation measurements

The effect of representing dielectric properties in terms of the complex polarizability ^c = – i is examined. Loss curves ( and tan ) are shifted towards higher frequencies, revealing the existence of new relaxations and allowing the clarifications of ones already known. We have calculated the shift ratios (at maximum or tan )/ (at maximum or tan ) from the more conventional empirical equations representing the dielectric behavior. Some examples are given.     

First chemical on-line separation and detection of a subsecond α-decaying nuclide, 224Pa

Subsecond ²²⁴ Pa (T _1/2 = 0.85 s) was produced via the ²⁰⁹ Bi(¹⁸ O,3n)²²⁴ Pa reaction at the 88 inch cyclotron at the Lawrence Berkeley National Laboratory. After production it was transported via a gas-jet system to the centrifuge system SISAK 3. Following on-line extraction with trioctylamine/scintillation solutions from 1M lactic acid, ²²⁴ Pa was detected applying on-line -liquid scintillation counting. Unambiguous identification was achieved using time-correlated --decay chain analysis. This constitutes the first chemical on-line separation and detection of a subsecond -decaying nuclide, 0.85-s ²²⁴ Pa with the fast extraction system SISAK 3.     

A further study of the substrate specificity in the reduction of 20-oxosteroids with a culture ofActinomyces roseochromogenus

Conclusions A culture ofActinomyces roseochromogenus ATCC 3347 reduces 17-hydroxy- and 16, 17-epoxy-20-oxopregnenes to the corresponding 20-alcohols, but is incapable of reducing 17-acetoxy-, 17-methyl-, and 16-methylprogesterones or 17-unsubstituted 20-oxopregnenes. The results obtained show that the presence of the side chain in a conformation favorable for the formation of 20-alcohols in the reduction of 20-oxosteroids with complex metal hydrides is in itself insufficient for the reduction of the 20-oxosteroids by a culture ofActinomyces roseochromogenus, which also reduces the 20-oxo group of 17-pregnenes.Khimiya Prirodnykh Soedinenii, Vol. 6, No. 1, pp. 38–47, 1970     

Alpha-counting with a solid scintillator

Alpha-counting with a commercial solid scintillator, LumaCap, in a liquid scintillation analyzer, has been studied. It has been found that LumaCap produces much more fluorescence than normal cocktail does, upon the reaction of -particles. Pulse height and pulse shape analysis have been applied for - and -discrimination successfully. This solid scintillator provides a useful means for -counting in normal liquid scintillation instruments.     

Transformed steroids

A preparative method for 9a-hydroxylation of ⁵-3-hydroxysteroids using the fungi ofCircinella sp. 10Kh-1220 not capable of modifying theA ring has been developed. It is established that the yields of the main and the side products greatly depend on the transformation conditions, mycelium age, and the structure of the steroid substrate. Under the optimal transformation conditions novel 9-hydroxysubstituted derivatives of androstenolone, pregnenolone, 16-dehydro-16,17-epoxy-, and-16-methoxypregnenolone have been obtained in 36–80 % yields.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 4, pp. 737–743, April, 1994.     

Transformed steroids. 189. Synthesis and transformations of 21-hydroxy-5α-H-pregnane 2′,2′-dimethyl-[16α,17α-d]-thioxalanes

In a continuation of the research on use of 20-keto-16,17-epoxysteroid 20-hydrazones for synthesis of 17-thio analogs of 20-ketosteroid 16,17-acetonides [2, 3], we synthesized 5-H-pregnane-3,16,21-trihydroxy-17-thiol-20-one 16,17-acetonide and found methods for its microbiological dehydrogenation and hydroxylation into ⁴-3-keto-and 9-hydroxy-⁴-3-keto derivatives.See [1] for Communication 188.N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 5, pp. 1182–1186, May, 1992.     

Karakanine — A new alkaloid from the epigeal part of Aconitum karakolicum

A new alkaloid, which has been called karakanine, has been isolated from the total alkaloids of the epigeal part ofAconitum karakolicum. The structure of karakanine as 8,14-dihydroxy-16-methoxy-4-methyl-N-ethyl-1,19-epoxyaconitane has been proposed on the basis of a study of its IR, PMR, mass, and¹³C NMR spectra, and has been confirmed by its conversion into karakoline.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedeninii, No. 1, pp. 62–64, January–February, 1993.     

Cardiac glycosides ofAcokanthera venenata

Six cardenolides have been isolated from the leaves ofAcokanthera venenata G. Don: AV-1, mp 252–255°C, [] _D ²⁰ +39.4° (MeOH); AV-2, mp 199–208°C, [] _D ²⁰ -59.3° (MeOH); AV-3, mp 269–275°C/300–304°C, [] _D ²¹ –69.8° (MeOH); AV-4, mp 279–289°C; AV-5, mp 222–225°, [] _D ²⁰ -64.3° (MeOH); and AV-6, mp 193–196°C [] _D ²⁰ –23.8° (MeOH — CHCl₃). AV-5 has been identified as acovenoside A. AV-3 is a new cardiac glycoside: it is 1-acetoxy-3-(4-O--D-glucosyl-3-O-methyl--L-talomethylosyloxy)-14-hydroxy-5, 14-card-20(22)-enolide (glucoacovenoside B).Khar'kov State Pharmaceutical Institute. All-Union Scientific Research Institute of Drug, Chemistry and Technology, Khar'kov. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 372–376, May–June, 1987.     

Pulchellin C and inuchinenolide C from Inula caspica

The pseudoguaianolide inuchinenolide C and the eudesmanolide pulchellin C have been isolated for the first time from the flower heads and leaves ofInula caspica Blume, and their spatial structures have been established by an x-ray structural experiment as 2,6-diacetoxy-6-hydroxy-1,7(H),8,10(H)-pseudoguai-11(13)-en-8,12-olide and 2,3-dihydroxy-5,7,8(H)-eudesma-4(15),11(13)-dien-8,12-olide, respectively.Institute of Organic Synthesis and Coal Chemistry, Academy of Sciences of the Kazakh SSR, Karaganda. A. N. Nesmeyanov Institute of Organometallic Compounds, Academy of Sciences of the USSR, Moscow. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 748–757, November–December, 1990.     

Triterpene glycosides ofCauliphyllum robustum. The structures of caulosides B and C

Summary Two triterpene glycosides — caulosides b and c — have been isolated from a methanolic extract of the leaves ofCaulophyllum robustum maxim. Cauloside b has been identified as hederagenin 3--L-rhamnopyranosyl-(12)--L-arabinopyranoside, while cauloside c has the structure of hederagenin 3-0--L-arabinopyranosyl(13)--L-pyranosyl-(12)--L-arabinopyranoside.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Scientific Center of the Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 174–176, March–April, 1979.