(C6H16N2)Zn3(HPO3)4H2O: a new layered zinc phosphite templated by diprotonated trans-1,4-diaminocyclohexane

International Nuclear Information System (INIS)

Wang Yu; Yu Jihong; Li Yi; Du Yu; Xu Ruren; Ye Ling

2003-01-01

Employing trans-1,4-diaminocyclohexane (trans-1,4-DACH) as a template, a new two-dimensional layered zinc phosphite (C 6 H 16 N 2 )Zn 3 (HPO 3 ) 4 H 2 O (1) has been prepared hydrothermally. Single-crystal X-ray diffraction analysis shows that it crystallizes in the monoclinic space group P2 1 /n with a=10.458(2) A, b=14.720(3) A, c=13.079(3) A, β=97.93(3) deg. , V=1994.1(7) A 3 , Z=4, R 1 =0.0349 (I>2σ(I)) and wR 2 =0.0605 (all data). The inorganic layer is built up by alternation of ZnO 4 tetrahedra and HPO 3 pseudo pyramids forming a 4.6.8-net. The sheet is featured by a series of capped six-membered rings. The diprotonated trans-1,4-DACH molecules reside in the interlayer region and interact with the inorganic network through H-bonds

129I Interlaboratory comparison: phase I and phase II

International Nuclear Information System (INIS)

Caffee, M. W.; Roberts, M. L.

1999-01-01

An interlaboratory comparison exercise for 129 I was organized and conducted. Nine laboratories participated in the exercise to either a full or limited extent. In Phase I of the comparison, 11 samples were measured. The suite of samples contained both synthetic ''standard type'' materials (i.e., AgI) and environmental materials. The isotopic 129 I/ 127 I ratios of the samples varied from 10 -8 to 10 -14 . In this phase, each laboratory was responsible for its own chemical preparation of the samples. In Phase I, the 129 I AMS measurements for prepared AgI were in good agreement. However, large discrepancies were seen in 129 I AMS measurements of environmental samples. Because of the large discrepancies seen in the Phase I 129 I intercomparison, a subsequent study was conducted. In Phase II of the 129 I intercomparison, three separate laboratories prepared AgI from two environmental samples (IAEA 375 soil and maples leaves). Each laboratory used its own chemical preparation method with each of the methods being distinctly different. The resulting six samples (two sets of three) were then re-distributed to the participating 129 I AMS facilities and 129 I/ 127 I ratios measured. Results and discussion of both the Phase I and Phase II interlaboratory comparison are presented

Measurement of gap and grain-boundary inventories of 129I in used CANDU fuels

International Nuclear Information System (INIS)

Stroes-Gascoyne, S.; Moir, D.L.; Kolar, M.; Porth, R.J.; McConnell, J.L.; Kerr, A.H.

1995-01-01

Combined gap and grain-boundary inventories of 129 I in 14 used CANDU fuel elements were measured by crushing and simultaneously leaching fuel segments for 4 h in a solution containing KI carrier. From analogy with previous work a near one-to-one correlation was anticipated between the amount of stable Xe and the amount of 128 I in the combined gap and grain-boundary regions of the fuel. However, the results showed that such a correlation was only apparent for low linear power rating (LLPR) fuels with an average linear power rating of 44 kW/m), the 129 I values were considerably smaller than expected. The combined gap and grain-boundary inventories of 129 I in the 14 fuels tested varied from 1.8 to 11.0%, with an average value of 3.6 ± 2.4% which suggests that the average value of 8.1 ± 1% used in safety assessment calculations overestimates the instant release fraction for 129 I. Segments of used CANDU fuels were leached for 92 d (samples taken at 5, 28 and 92 d) to determine the kinetics of 129 I release. Results could be fitted tentatively to half-order reaction kinetics, implying that 129 I release is a diffusion-controlled process for LLPR fuels, and also for HLPR fuels, once the gap inventory has been leached. However, more data are needed over longer leaching periods to gain more understanding of the processes that control grain-boundary release of 129 I from used CANDU fuel

Chemical speciation analysis and environmental behaviour of 127I and 129I

Energy Technology Data Exchange (ETDEWEB)

Hansen, Violeta

2011-10-15

Chemical speciation analysis of 129I and 127I as iodide, iodate and total inorganic iodine in seawater samples from the Baltic Proper, Skagerrak and Kattegat has been carried out. The important findings of this study are that the reduction of iodate and oxidation of iodide in Skagerrak and Kattegat may be a slow process while along the Baltic Sea surface water reduction of iodate is a relatively fast process. Although suboxic or anoxic condition are encountered in some of the Baltic Sea deep basins, the concentration of 129IO{sub 3}- increases with water depth indicating that the reduction of iodate in the oxygen deficient bottom water of the Baltic Sea is a slow process. Iodine chemical speciation analysis (as iodide, iodate and total iodine including inorganic and organic iodine species) in lake water samples collected from Denmark and southern Sweden has been carried out. Destruction of organic iodine was performed by alkaline oxidation using NaOH - NaClO at 100 deg. C and anion exchange chromatography was used for separation of iodide and iodate. Iodine-129 concentrations in the lakes ranged from 1.3 - 12.8 x109 at/L and show elevated concentrations in lakes located in southwest Jutland (Denmark), near the North Sea. Except the Skaersoe Lake, were the organic iodine - 127 accounts for 50% of the total iodine, iodide (both 129I and 127I) is the predominant species form in surface water of the studied lakes. An investigation was conducted in order to quantify the total aquatic iodine (129I and 127I as inorganic and organic iodine) from fresh water and seawater samples by adsorption onto activated charcoal and DEAE 32 cellulose followed by alkaline digestion or combustion. The results show that iodide from freshwater samples can easily be adsorbed onto activated charcoal. The sorption was not affected by the pH. The absorption capacity of iodate is low and reduces quickly when its concentration increases. Compared with activated charcoal, DEAE 32 cellulose showed

14 CFR 129.25 - Airplane security.

Science.gov (United States)

2010-01-01

... 14 Aeronautics and Space 3 2010-01-01 2010-01-01 false Airplane security. 129.25 Section 129.25 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR CARRIERS... AND FOREIGN OPERATORS OF U.S.-REGISTERED AIRCRAFT ENGAGED IN COMMON CARRIAGE General § 129.25 Airplane...

Comprehensive analysis of collagen metabolism in vitro using [4(3H)]/[14C]proline dual-labeling and polyacrylamide gel electrophoresis

International Nuclear Information System (INIS)

Bateman, J.F.; Harley, V.; Chan, D.; Cole, W.G.

1988-01-01

A method to simultaneously quantify the production, secretion, and prolyl hydroxylation of individual types of collagen in cell culture samples has been developed. Collagens were biosynthetically labeled with a mixture of [ 14 C]proline and [4- 3 H]proline. The labeled collagens were isolated and their component alpha-chains were resolved by sodium dodecyl sulfate/polyacrylamide gel electrophoresis. Migration of the collagen alpha-chains was determined by fluorography, and radioactivity in excised bands was quantified by scintillation counting. [ 14 C]Proline labeling of collagen chains was used to determine the production and secretion of the different types of collagen. The ratios of the component alpha 1(I) and alpha 2(I) chains of type I collagen were also determined in this way. Prolyl hydroxylation of collagen alpha-chains was readily determined by measurement of their 3 H: 14 C ratios. Following 4-hydroxylation, 3 H was lost from the [4-3H]proline with alteration of this ratio. This dual-labeling method is suitable for the comprehensive analysis of collagen metabolism in multiple samples

Pyrrolophenanthridines. I. Synthesis of 2!H and 13C NMR spectra of 1H-pyrrolo[2,3-c]- and 1H-pyrrolo[3,2-i]-phenanthridines

International Nuclear Information System (INIS)

Frolova, E.P.; Akhvlediani, R.N.; Krasnokut-skii, S.N.; Kurkovskaya, L.N.; Suvorov, N.N.

1987-01-01

A preparative method is proposed for the synthesis of 3- and 8-aminophenanthridines, from which the new heterocyclic systems 1H-pyrrolo[2,3-c]- and 1H-pyrrolo[3,2-i]phenanthridines were synthesized by means of the Fischer reaction

Synthesis of binuclear rhodacarboranes from dianions 1,4- and 1,3-C6H4(CH2-9-C2H2B9H9-7,8-nido)22- and (Ph3P)3RhCl

International Nuclear Information System (INIS)

Zakharkin, L.I.; Zhigareva, G.G.

1996-01-01

Dianions 1,4 and 1,3-C 6 H 4 (CH 2 -9-C 2 H 2 B 9 H 9 -7,8-nido) 2 2- obtained from nido 7,8-dicarbollide-ion and 1,4-bis(bromomethyl) and 1,3-bis(bromomethyl)benzenes react with (Ph 3 P) 3 RhCl to give binuclear rhodacarboranes, 1,4- and 1,3-[3,3-(Ph 3 P) 2 -3-H-3,1,2-RhC 2 B 9 H 10 -4-CH 2 ] 2 C 6 H 6 with chemical reaction yield 85% and 87% respectively. 7 refs., 1 fig., 1 tab

Environmental 14C and 3H activities: global trends and local contamination

International Nuclear Information System (INIS)

Krajcar Bronic, I.; Obelic, B.; Horvatincic, N.

2000-01-01

The anthropogenic disturbance of natural distributions of radiocarbon ( 14 C) and tritium ( 3 H) due to the release of bomb-produced isotopes occurred after the World War II and at the same time the monitoring of these isotopes started at several stations in the world. Radioactive isotopes 14 C and 3 H, together with the stable isotopes 2 H and 18 O, are very important tracers in environmental, climatological and hydrological studies. Monitoring of environmental levels of 14 C and 3 H in Croatia started more then 20 years ago, while that of the stable isotopes somewhat later. The monitoring was performed at the three types of stations: a) 'clean-air' sites, which are supposed to reflect only the global disturbance of the atmospheric isotope concentrations, b) in a densely populated industrial center, where the effect of intense fossil-fuel combustion is expected, and local contamination from institutions using radioactive-labeled material is also possible, and c) at locations around the Nuclear Power Plant Krsko. The mean yearly 3 H activities in precipitation continuously decrease since the beginning of monitoring approaching slowly the natural equilibrium. The monthly 3 H activities show seasonal variations, with maximum in early summer and minimum in early winter. Both seasonal variations and the decrease of the mean yearly values are typical for continental stations of the Northern Hemisphere. At the sampling site located at the Institute, several periods of higher 3 H activities were observed, due to the local contamination with the tritium-labeled material. The 14 C concentration in the atmosphere shows also the continuous decrease of the mean yearly values and superposed seasonal fluctuations, with higher activity during summer. Seasonal peak-to-peak variations are higher in the area of the city of Zagreb than at the clean-air site on the mountain (about 1000 m a.s.l.). This difference is caused by the introduction of CO 2 (containing no 14 C isotope

¹²⁷I and ¹²⁹I Species and Transformation in the Baltic Proper, Kattegat, and Skagerrak Basins

DEFF Research Database (Denmark)

Yi, P.; Aldahan, A.; Possnert, G.

2012-01-01

, high 127I–/127IO3– and 129I–/129IO3– values suggest effective reduction of iodate with a maximum rate of 8 × 10–7 (127IO3–) and 6 × 10–14 (129IO3–) (g/m3.day). The reduction process of iodate seems to be related to decomposition of organic matter and photochemically induced reactions.......Occurrence of anthropogenic 129I in seawater has provided invaluable information about water circulation and exchange rates, but results on 129I species (iodide and iodate) are limited and only available for surface water. We here present the first extensive results on 129I and 127I species...

I-129 migration and retrospective dosimetry

International Nuclear Information System (INIS)

Daraoui, Abdelouahed

2010-01-01

The naturally occurring of the long-lived radionuclide 129 I (T 1/2 = 15.7 Ma) have been substantially increased by the fallout from atmospheric nuclear explosions, by releases from nuclear accidents and by emissions from reprocessing plants. The aim of this study was to determine the 127 I, 129 I, 40 K and 137 Cs in Soils from Northern Ukraine, Chile, Bavaria and the Retrospective Dosimetry of the 131 I exposure after the Chernobyl Accident. In addition, water samples from North Germany (precipitation, surface and ground waters, Aerosol, soils, Humus and milk), North Sea, North Atlantic, Spitzbergen, Indian Ocean, Mediterranean, Hawaii, Tahiti, Egypt and prenuclear sediment samples of the Baltic Sea and the North Sea were analysed. 129 I/ 127 I was analysed by accelerator mass spectrometry (AMS) and 127 I was determined by inductively coupled plasma mass spectrometry (ICP-MS). The geometric mean deposition density of 129 I in these soils was 109 x 1.5 ±1 mBq m -2 , that the dominant sources of 129 I in the region are the reprocessing plants (La Hague and Sellafield) and not the Chernobyl fallout. The 129 I/ 127 I isotopic ratios of the Bavarian soils are measured between 10 -7 and 10 -10 what is 100- to 1000-time higher than as the ratios obtained for the Chilean samples. The 129 I integral deposition densities in Chile, Easter Island and Antarctica were between 0.3 and 2 mBq m -2 . In these soils the observed 129 I/ 127 I ratios are about 10 -12 low measured Value in the pedosphere. This value is consistent with the results from the marine sediments assumed to represent the pre-nuclear equilibrium ratios. The soils from Chile also allow the determination of the 129 I fallout from the atmospheric nuclear weapons explosions undisturbed from contaminations due to the releases from reprocessing plants. The results from the soil profiles show that more than 90 % of the 129 I-concentration in the soil profiles are still in the top 40 cm of the profiles is located

Dicty_cDB: SSK129 [Dicty_cDB

Lifescience Database Archive (English)

Full Text Available SS (Link to library) SSK129 (Link to dictyBase) - - - Contig-U16021-1 SSK129Z (Link... to Original site) - - SSK129Z 372 - - - - Show SSK129 Library SS (Link to library) Clone ID SSK129 (Link to dict...yBase) Atlas ID - NBRP ID - dictyBase ID - Link to Contig Contig-U16021-1 Original site URL http://dict...Homology vs DNA Score E Sequences producing significant alignments: (bits) Value N AC116957 |AC116957.2 Dict...419632 |CK419632.1 AUF_IpOva_21_i24 Ovary cDNA library Ictalurus punctatus cDNA 5', mRNA sequence. 36 0.54 2

14 CFR 129.28 - Flightdeck security.

Science.gov (United States)

2010-01-01

... 14 Aeronautics and Space 3 2010-01-01 2010-01-01 false Flightdeck security. 129.28 Section 129.28... Flightdeck security. (a) After August 20, 2002, except for a newly manufactured airplane on a non-revenue...; or the operator must implement a security program approved by the Transportation Security...

Investigations on the 129I radioecology

International Nuclear Information System (INIS)

Schuettelkopf, H.

1977-01-01

The measurement of 129 I concentrations in milk and soil samples was continued. In process solutions of the Karlsruhe Reprocessing Plant the 129 I concentrations were determined. 127 I was measured in air. Apparatus for the collection of 127 I in air were installed in Kiel, Stade and Gundremmingen. The concentrations of 129 I in goats milk were between 0.03 and 1.1 pCi/g. The soil sample concentrations were between 0.3 and 5.6 fCi/g. The concentrations of 127 I in air from the environment of the Karlsruhe Nuclear Research Center averages about 10 ng I 2 /m 3 and about 2 ng aerosol bound I/m 3 . (orig./RW) [de

Cluster-enhanced X-O-2 photochemistry (X=CH3I, C3H6, C6H12, and Xe)

NARCIS (Netherlands)

Baklanov, A.V.; Bogdanchikov, G.A.; Vidma, K.V.; Chestakov, D.A.; Parker, D.H.

2007-01-01

The effect of a local environment on the photodissociation of molecular oxygen is investigated in the van der Waals complex X-O-2 (X=CH3I, C3H6, C6H12, and Xe). A single laser operating at wavelengths around 226 nm is used for both photodissociation of the van der Waals complex and simultaneous

Differential blood-brain barrier permeabilities to [14C]sucrose and [3H]inulin after osmotic opening in the rat

International Nuclear Information System (INIS)

Ziylan, Y.Z.; Robinson, P.J.; Rapoport, S.I.

1983-01-01

The blood-brain barrier (B-BB) in 3-month-old rats was opened unilaterally by infusing 1.8 m L(+)arabinose in water into the internal carotid artery through a catheter in the external carotid. Two poorly penetrating uncharged test radiotracers of differing molecular weight and size, [ 14 C]sucrose (340 daltons, radius 5 A) and [ 3 H]inulin (5500 daltons, radius 15 A), were simultaneously injected i.v. in untreated rats, or rats at 1, 30, or 50 min after infusion of hypertonic arabinose solution. Evans-blue solution was injected 5 min prior to osmotic treatment as a visual indicator of barrier integrity. In regions of uninfused control brains, the [ 14 C]sucrose permeability-surface area (PA) product approximated 10(-5) s-1, whereas PA was not measurable for [ 3 H]inulin. In arabinose-infused animals, PA products on the ipsilateral hemisphere for both [ 14 C]sucrose and [ 3 H]inulin were markedly elevated 6 min after infusion, but decreased by 35 and 55 min. In nearly all regions, statistically significant differences were not found between 6-min [ 14 C]sucrose- and [ 3 H]inulin-PA values (P greater than 0.05). However, at 35 and 55 min in most regions, the PA for [ 3 H]inulin was significantly lower (P less than 0.05) than PA for [ 14 C]sucrose. The results indicated that the B-BB closed more rapidly to larger than to smaller molecules after osmotic treatment and were consistent with a pore model for osmotic B-BB opening

Speciation analysis of 129I in seawater by carrier-free AgI-AgCl coprecipitation and accelerator mass spectrometric measurement

DEFF Research Database (Denmark)

Luo, Maoyi; Hou, Xiaolin; He, Chaohui

2013-01-01

A rapid and simple method was developed for speciation analysis of 129I in seawater by selective coprecipitation of carrier-free iodide and accelerator mass spectrometry (AMS) measurement of 129I. Iodide was separated from seawater and other species of iodine by coprecipitation of AgI with Ag2SO3......, AgCl, and AgBr by addition of only 100 mg/L Ag+ and 0.3 mmol/L NaHSO3 at pH 4.2-5.5. The separation efficiency of iodide was more than 95%, and crossover between 129IO3- and 129I- fractions is less than 3%. Iodate and total inorganic iodine were converted to iodide by use of NaHSO3 at pH 1......-2 and then separated by the same method as for iodide. Ag2SO3 in the coprecipitate was removed by washing with 3 mol/L HNO3 and the excess AgCl and AgBr was removed by use of diluted NH3, and finally a 1-3 mg precipitate was obtained for AMS measurement of 129I. The recovery of iodine species in the entire procedure...

Efficient method of enzymatic synthesis of nucleosides labelled with 14C and 3H

International Nuclear Information System (INIS)

Nejedly, Z.; Filip, J.

1988-01-01

The method is presented of enzymatic synthesis of nucleosides labelled with 14 C or 3 H either uniformly or specifically in the base or the deoxyribosyl or ribosyl moiety. The method is based on the ribosylation or deoxyribosylation of the nucleic acid bases (non-labelled or labelled with 14 C or 3 H) by the catalytic effect of enzymes occurring in the supernatant fractions of non-purified homogenates of Escherichia coli B. bacteria. The non-labelled and labelled nucleosides are used as donors of ribosyl or deoxyribosyl groups. The HPLC method is used for separating labelled nucleosides. The radiochemical purity of the labelled nucleosides is higher than 98%, molar activity ranges from 9.2 to 18.5 GBq.mmol -1 ( 14 C-labelled compounds) and from 0.6 to 1.9 TBq.mmol -1 (3H-labelled compounds). (author). 4 figs., 8 refs

The 14-3-3 protein interacts directly with the C-terminal region of the plant plasma membrane H(+)-ATPase

DEFF Research Database (Denmark)

Jahn, T.; Fuglsang, A.T.; Olsson, A.

1997-01-01

Accumulating evidence suggests that 14-3-3 proteins are involved in the regulation of plant plasma membrane H(+)-ATPase activity. However, it is not known whether the 14-3-3 protein interacts directly or indirectly with the H(+)-ATPase. In this study, detergent-solubilized plasma membrane H...... plasma membrane H(+)-ATPase. We propose that the 14-3-3 protein is a natural ligand of the plasma membrane H(+)-ATPase, regulating proton pumping by displacing the C-terminal autoinhibitory domain of the H(+)-ATPase....

C-14/I-29 Preservation and Hold Time Survey

Energy Technology Data Exchange (ETDEWEB)

Kitchen, S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2015-04-08

Preservation and hold time of radionuclides must account for both nuclear half-lives and nonnuclear loss mechanisms, but variations in the latter are often neglected. Metals-based defaults are inappropriate for long-lived non-metals C-14 and I-129, which are vulnerable to chemical and biological volatilization. Non-acidification is already widely practiced for them. Recommended addition measures from radiological and chemical literature include glass containers where possible, water filtration where possible, headspace minimization, light shielding, cold (4°C) storage and unfiltered water hold time of 28 days. Soil hold time may need to be shortened when water-logged, excessively sandy, or still adjusting to significant new contamination.

Double labeling autoradiography. Cell kinetic studies with 3H- and 14C-thymidine

International Nuclear Information System (INIS)

Schultze, B.

1981-01-01

Examples of the multiple applicability of the double labeling method with 3 H- and 14 C-TdR are demonstrated. Double labeling with 3 H- and 14 C-TdR makes it possible to determine the cycle and its phases with high precision by modifying the usual percent labeled mitoses method with a single injection of 3 H-TdR. In addition, data is provided on the variances of the transit times through the cycle phases. For example, in the case of the jejunal crypt cells of the mouse, the transit times through successive cycle phases are uncorrelated. In the case of glial cells the double labeling method provides cell kinetic parameters despite the paucity of proliferating glial cells. In the adult untreated animal, glial cell mitoses are so rare that the percent labeled mitoses method can not be utilized. However, the S-phase duration can be measured by double labeling and the cycle time can be determined by the so-called method of labeled S phases. With the latter method the passage through the S phase of the 3 H-TdR-labeled S phase cells can be registered by injecting 14 C-TdR at different time intervals following 3 H-TdR application. In this way an S-phase duration of about 10 hr and a cycle time of about 20 hr was found for glial cells in the adult untreated mouse. An exchange of glial cells between the growth fraction and the nongrowth fraction has also been shown by double labeling. A quite different application of the double labeling method with 3H- and 14 C-TdR is the in vivo study of the cell cycle phase-specific effect of drugs used in chemotherapy of tumors. The effect of vincristine on these cells has been studied. Vincristine affects cells in S and G2 in such a manner that they are arrested during the next metaphase and subsequently become necrotic. It has no effect on G1 cells

Crystal structure, quantum mechanical investigation, IR and NMR spectroscopy of two new organic perchlorates: (C6H18N3)·(ClO4)3H2O (I) and (C9H11N2)·ClO4(II)

Science.gov (United States)

Bayar, I.; Khedhiri, L.; Soudani, S.; Lefebvre, F.; Ferretti, V.; Ben Nasr, C.

2018-06-01

The reaction of perchloric acid with 1-(2-aminoethyl)piperazine or 5,6-dimethyl-benzimidazole results in the formation of 1-(2-amonioethyl)piperazine-1,4-dium triperchlorate hydrate (C6H18N3)·(ClO4)3·H2O (I) or 5,6-dimethyl-benzylimidazolium perchlorate (C9H11N2)·ClO4(II). Both compounds were fully structurally characterized including single crystal X-ray diffraction analysis. Compound (I) crystallizes in the centrosymmetric triclinic space group P 1 bar with the lattice parameters a = 7.455 (2), b = 10.462 (2), c = 10.824 (2) Å, α = 80.832 (2), β = 88.243 (2), γ = 88.160 (2) °, Z = 2 and V = 832.77 (3) Å3. Compound (II) has been found to belong to the P21/c space group of the monoclinic system, with a = 7.590 (3), b = 9.266 (3), c = 16.503 (6) Å, β = 107.38 (2) °, V = 1107.69 (7) Å3 and Z = 4. The structures of (I) and (II) consist of slightly distorted [ClO4]- tetrahedra anions and 1-(2-amonioethyl)piperazine-1,4-dium trication (I) or 5,6-dimethyl-benzylimidazolium cations (II) and additionally a lattice water in (I). The crystal structures of (I) and (II) exhibit complex three-dimensional networks of H-bonds connecting all their components. In the atomic arrangement of (I), the ClO4- anions form corrugated chains, while in (II) the atomic arrangement exhibits wide pseudo-hexagonal channels of ClO4 tetrahedra including the organic entities. The lattice water serves as a link between pairs of cations and pairs of anions via several Osbnd H⋯O and N-H⋯O interactions in compound (I). The vibrational absorption bands were identified by infrared spectroscopy. These compounds were also investigated by solid-state 13C, 35Cl and 15N NMR spectroscopy. DFT calculations allowed the attribution of the IR and NMR bands. Intermolecular interactions were investigated by Hirshfeld surfaces. Electronic properties such as HOMO and LUMO energies were derived.

The radioactivity estimation of 14C and 3H in graphite waste samples of the KRR-2.

Science.gov (United States)

Reyoung Kim, Hee

2013-09-01

The radioactivity of (14)C and (3)H in graphite samples from the dismantled Korea Research Reactor-2 (the KRR-2) site was analyzed by high-temperature oxidation and liquid scintillation counting, and the graphite waste was suggested to be disposed of as a low-level radioactive waste. The graphite samples were oxidized at a high temperature of 800 °C, and their counting rates were measured by using a liquid scintillation counter (LSC). The combustion ratio of the graphite was about 99% on the sample with a maximum weight of 1g. The recoveries from the combustion furnace were around 100% and 90% in (14)C and (3)H, respectively. The minimum detectable activity was 0.04-0.05 Bq/g for the (14)C and 0.13-0.15 Bq/g for the (3)H at the same background counting time. The activity of (14)C was higher than that of (3)H over all samples with the activity ratios of the (14)C to (3)H, (14)C/(3)H, being between 2.8 and 25. The dose calculation was carried out from its radioactivity analysis results. The dose estimation gave a higher annual dose than the domestic legal limit for a clearance. It was thought that the sampled graphite waste from the dismantled research reactor was not available for reuse or recycling and should be monitored as low-level radioactive waste. Copyright © 2013 Elsevier Ltd. All rights reserved.

Partition of iodine (129I and 127I) isotopes in soils and marine sediments

DEFF Research Database (Denmark)

Hansen, Violeta; Roos, Per; Aldahan, Ala

2011-01-01

Natural organic matter, such as humic and fulvic acids and humin, plays a key role in determining the fate and mobility of radioiodine in soil and sediments. The radioisotope 129I is continuously produced and released from nuclear fuel reprocessing plants, and as a biophilic element, its......–60% of the total 129I are associated with organic matter in soil and sediment samples. At a soil/sediment pH below 5.0–5.5, 127I and 129I in the organic fraction associate primarily with the humic acid while at soil/sediment pH > 6 129I was mostly found to be bound to fulvic acid. Anoxic conditions seem...... environmental mobility is strongly linked to organic matter. Due to its long half-life (15.7 million years), 129I builds up in the environment and can be traced since the beginning of the nuclear era in reservoirs such as soils and marine sediments. Nevertheless, partition of the isotope between the different...

Distribution of 129I: Evidence for world-wide influence of nuclear fuel reprocessing

International Nuclear Information System (INIS)

Fehn, U.; Snyder, G.; Moran, J.E.

1999-01-01

Iodine-129 is one of the radioisotopes which have seen significant increases in the environment since the beginning of the nuclear age. Other prominent representatives of this group include tritium, 14 C and 36 Cl. Most members of this group have gone through a cycle of initial release (associated mainly with atmospheric bomb tests during the late fifties and early sixties) and subsequent decay (e.g. T) or dispersion (e.g. 14 C and 36 Cl) so that their concentrations are again close to pre-anthropogenic levels. 129 I has, however, remained at significantly elevated levels even after the stop of nuclear weapon tests

Evaluation of radiation dose resulting from the ingestion of [3H]-and [14C]thymidine in the rat

International Nuclear Information System (INIS)

Takeda, H.; Iwakura, T.

1987-01-01

Average doses to rat tissues from the ingestion of 2-[ 14 C]thymidine were compared with those from methyl-[ 3 H]thymidine or 6-[ 3 H]thymidine. [ 14 C]thymidine gave the highest dose to spleen and small intestine. Doses to other tissues from [ 14 ]thymidine were almost the same or lower compared with those from [ 3 H]thymidine, irrespective of the 9 times higher β-ray energy of 14 C than that of 3 H. In the case of [ 14 C]thymidine, most of the dose was given by radioactivity incorporated into the organic tissue constituents (non-volatile radioactivity). In the case of [ 3 H]thymidine, the dose contributions by non-volatile radioactivity were very small and major contributions were rather from volatile radioactivity ( 3 HHO), formed by degradation of [ 3 H]thymidine. No significant difference in their total doses was found between the two [ 3 H]precursors, but the dose from non-volatile radioactivity alone was 2-3 times higher with methyl-[ 3 H]thymidine than with 6-[ 3 H]thymidine. Estimates of dose to cell nuclei in various tissues after ingestion of [ 3 H]thymidine were also made in order to predict more precisely possible radiation hazards. (author)

14C2H4: distribution of 14C-labeled tissue metabolites in pea seedlings

International Nuclear Information System (INIS)

Giaquinta, R.; Beyer, E. Jr.

1977-01-01

The 14 C-metabolite distribution pattern following 14 C 2 H 4 metabolism in intact pea seedlings (Pisum sativum L.) was determined under various conditions. After a 24 hr exposure to 14 C 2 H 4 , the majority of 14 C-metabolites were water-soluble (60-70%) with lesser amounts in the protein (10-15%), lipid (1%), and insoluble (1-2%) fractions. Ion exchange chromatography of the water-soluble components into basic, neutral, and acidic fractions revealed a 50:40:10 distribution, respectively. Chromatography of the neutral fraction revealed two regions of radioactivity (Rf=0.38) and 0.63 which did not cochromatograph with twenty-two known sugars or neutral metabolites. Chromatograms of the basic fraction contained 3 regions of radioactivity. Similar distribution patterns were noted when 14 C 2 H 4 exposure was followed by a 6 hr air chase or when 5% CO 2 , an antagonist of ethylene action, was present during the exposure. Marked differences in the 14 C-metabolite distribution patterns were obtained when 14 CO 2 was substituted for 14 C 2 H 4 . These results indicate that the metabolic pathway involved in ethylene metabolism is different from that involved in intermediately carbon metabolism. (auth.)

Labelling by 14C and 3H on 4,4-dimethyl-1-(3,4-methylenedioxyphenyl)-1-pentene-3-ol or stiripentol

International Nuclear Information System (INIS)

Madelmont, J.C.; Rapp, M.; Labarre, P.; Maurizis, J.C.; Dupuy, J.M.; Lepage, F.; Veyre, A.

1992-01-01

4,4-dimethyl-1-(3,4-methylenedioxyphenyl)-1-pentene-3-ol or stiripentol was labelled by 14 C and 3 H. 14 C labelling was performed on the carbon 1 of the pentene group via a four step procedure. The radiochemical yield calculated from the precursor (Ba 14 CO 3 ) is 28%. 3 H labelling was performed on the position 3 of the pentene chain by reduction of the corresponding ketone via NaBT 4 . The radiochemical yield calculated from the precursor (NaBT 4 ) is 40%. (author)

Synthesis of 1-(2,3-dihydroxypropyl)-2-nitro-1H-imidazole-2-14C and N-(2-hydroxyethyl)-2-(2-nitro-1H-imidazol-1-YL-2-14C)acetamide

International Nuclear Information System (INIS)

Fong, M.T.; Leaffer, M.A.

1986-01-01

We have prepared the 14 C-labeled analogs of NSC 261036, 1-(2,3-dihydroxypropyl)-2-nitro-1H-imidazole-2- 14 C, and NSC 301467, N-(2-hydroxyethyl)-2-(2-nitro-1H-imidazol-1-yl-2- 14 C) acetamide, for pharmacological, drug distribution, and mechanisms of action studies. The latter is an analog designed for lower toxicity and improved properties. The former is a metabolite of, and appears to be less toxic than, misonidazole. (author)

Labelling by [sup 14]C and [sup 3]H on 4,4-dimethyl-1-(3,4-methylenedioxyphenyl)-1-pentene-3-ol or stiripentol. Marquage par [sup 14]C et [sup 3]H du 4,4-dimethyl-1-(methylendioxy-3,4 phenyl)-1-petene-3-ol ou stiripentol

Energy Technology Data Exchange (ETDEWEB)

Madelmont, J.C.; Rapp, M.; Labarre, P.; Maurizis, J.C. (Institut National de la Sante et de la Recherche Medicale (INSERM), 63 - Clermont-Ferrand (France)); Dupuy, J.M. (Centre Jean Perrin, Clermont-Ferrand (France)); Lepage, F. (Laboratoires BIOCODEX, Compiegne (France)); Veyre, A. (Clermont-Ferrand-1 Univ., 63 - Aubiere (France))

1992-11-01

4,4-dimethyl-1-(3,4-methylenedioxyphenyl)-1-pentene-3-ol or stiripentol was labelled by [sup 14]C and [sup 3]H. [sup 14]C labelling was performed on the carbon 1 of the pentene group via a four step procedure. The radiochemical yield calculated from the precursor (Ba[sup 14]CO[sub 3]) is 28%. [sup 3]H labelling was performed on the position 3 of the pentene chain by reduction of the corresponding ketone via NaBT[sub 4]. The radiochemical yield calculated from the precursor (NaBT[sub 4]) is 40%. (author).

Method for combined 3H and 14C autoradiography with a single emulsion tested in cultured mammalian cells

International Nuclear Information System (INIS)

Perdue, S.W.; Kimball, R.F.; Hsie, A.W.

1977-01-01

A single-gelatin expanded film method for double-isotope autoradiography is described. A preliminary classification based upon silver-grain distribution is used to assign labeled cells to 3 H only or with 14 C classes. Optical sectioning combined with grain counting is employed to obtain ratios for classifying cells labeled with 14 C into 14 C only and 3 H + 14 C classes. The method has been tested with CHO-K1 cells in plateau-phase cultures using two 24-h labeling periods. The experimental design allowed for independent estimation of the expected frequencies of label classes under conditions that provided a wide range of possible label levels and combinations. Previous methods have used time-consuming applications of two emulsion layers and exposures to distinguish between cells labeled with 3 H only or with 14 C and do not identify the 3 H + 14 C class. A single-gelatin expanded film requires only one exposure and permits all label classes to be determined by an objective grain-counting procedure

Synthesis of 14C- and 3H-labeled fluoxetine, a selective serotonin uptake inhibitor

International Nuclear Information System (INIS)

Robertson, D.W.; Krushinski, J.H.; Wong, D.T.; Kau, D.

1987-01-01

Fluoxetine (N-methyl-γ-(4-(trifluoromethyl)phenoxy) benzenepropanamine) is a potent, highly selective serotonin uptake inhibitor that is useful in treating a variety of major psychiatric derangements. We have synthesized this compound in 14 C- and 3 H-labeled forms. The tritium label was introduced in the final step by catalytic dehalogenation of the brominated fluoxetine precursor. Reaction conditions could be controlled such that catalytic hydrogenolysis of the labile C-O benzylic bond was minimized. Following HPLC purification, [ 3 H]-fluoxetine was obtained in a state of high radiochemical purity (98%) and specific activity (20.4 Ci/mmol). The 14 C-label was introduced in the final step via a nucleophilic aromatic substitution reaction between the sodium salt of α-(2-(methylamino)ethyl)benzenemethanol and uniformly ring-labeled p-chlorobenzotrifluoride. Following purification by flash chromatography, [ 14 C]-fluoxetine was obtained in 98.3% radiochemical purity with a specific activity of 5.52 mCi/mmol. (author)

Effects of hyperglycemia on glucose production and utilization in humans. Measurement with [3H]-2-, [3H]-3-, and [14C]-6-glucose

International Nuclear Information System (INIS)

Bell, P.M.; Firth, R.G.; Rizza, R.A.

1986-01-01

Studies with tritiated isotopes of glucose have demonstrated that hyperglycemia per se stimulates glucose utilization and suppresses glucose production in humans. These conclusions rely on the assumption that tritiated glucose provides an accurate measure of glucose turnover. However, if in the presence of hyperglycemia the isotope either loses its label during futile cycling or retains its label during cycling through glycogen, then this assumption is not valid. To examine this question, glucose utilization and glucose production rates were measured in nine normal subjects with a simultaneous infusion of [ 3 H]-2-glucose, an isotope that may undergo futile cycling but does not cycle through glycogen; [ 14 C]-6-glucose, an isotope that may cycle through glycogen but does not futile cycle; and [ 3 H]-3-glucose, an isotope that can both undergo futile cycling and cycle through glycogen. In the postabsorptive state at plasma glucose concentration of 95 mg X dl-1, glucose turnover determined with [ 14 C]-6-glucose (2.3 +/- 0.1 mg X kg-1 X min-1) was greater than that determined with [3 3 H]glucose (2.1 +/- 0.1 mg X kg-1 X min-1, P = 0.002) and slightly less than that determined with [ 3 H]-2-glucose (2.7 +/- 0.2 mg X kg-1 X min-1, P = 0.08). Plasma glucose was then raised from 95 to 135 to 175 mg X dl-1 while insulin secretion was inhibited, and circulating insulin, glucagon, and growth hormone concentrations were maintained constant by infusion of these hormones and somatostatin. Glucose production and utilization rates determined with [ 14 C]-6-glucose continued to be less than those determined with [ 3 H]-2-glucose and greater than those seen with [ 3 H]-3-glucose

Synthesis of two S-(methyl-3H)-labelled enkephalins and S-(methyl-14C) substance P

International Nuclear Information System (INIS)

Naegren, K.; Laangstroem, B.; Franzen, H.M.; Ragnarsson, U.

1988-01-01

The synthesis of 3 H-labelled Met-enkephalin and Tyr-D-Ala-Gly-Phe-Met-NH 2 (DALA) and 14 C-labelled Substance P (SP) from previously described, fully protected intermediates is reported. The labelled peptides were prepared by methylation with ( 3 H)- or ( 14 C)methyl iodide of the sulphide anions formed on deprotection of the corresponding S-benzyl-homocysteine precursors with sodium in liquid ammonia. After purification by LC, the labelled peptides were obtained in radiochemical yields in the range of 9 to 24% with a radiochemical purity higher than 97%. The specific radioactivities of the 3 H- and 14 C- labelled products, corresponding to the labelled methyl iodides used, were 80 mCi/μmol and 60 μCi/μmol, respectively. (author)

Energy Metabolism and Transfer of {sup 3}H and {sup 14}C in Mammals and Birds - Energy metabolism and transfer of {sup 3}H and {sup 14}C in mammals, birds, and fish

Energy Technology Data Exchange (ETDEWEB)

Melintescu, Anca; Galeriu, Dan [' Horia Hulubei' National Institute for Physics and Nuclear Engineering, Department of Environmental Physics and Life, 30 Reactorului St., POB MG-6, Bucharest-Magurele, RO-077125 (Romania); Beresford, Nicholas A. [NERC Centre for Ecology and Hydrology, Lancaster Environment Centre, Library Av. Bailrigg, Lancaster LA1 4AP (United Kingdom)

2014-07-01

The transfer of {sup 3}H and {sup 14}C in environment needs to be modelled differently than that of other radionuclides released from nuclear facilities because hydrogen and carbon are key components of biological tissues and the carbon and hydrogen life cycles. A detailed understanding of the behaviour of {sup 3}H and {sup 14}C in the food chain is essential because {sup 3}H may be released in large quantities from CANDU (Canadian Deuterium Uranium) reactors and future thermonuclear reactors, and {sup 14}C accumulates in the environment because of its long half-life. In recent years, the authors published both a simple and a complex dynamic metabolic model for {sup 3}H and {sup 14}C transfer to farm and wild animals. The models applications for wild animals were restricted to few examples. There is an increased interest to extend the models for a larger selection of wild animals, birds and fish to support developments such as the International Commission for Radiological Protection (ICRP) environmental protection framework. In this paper we describe activities to expand {sup 3}H and {sup 14}C models to cover a wider range of wildlife. The updated model of the dynamics of tritium transfer in aquatic food chains (AQUATRIT model) developed by the authors was successfully tested for small and large (trout) fish. Wild mammals and birds generally have a lower fat content than domestic species and must adapt to variable environmental conditions. The body mass is an important parameter involved in radionuclide transfer. The environmental temperature, type of animal, and diet must also be considered. The model input parameters for wild mammals are poorly defined because the experimental data are too few and the intraspecific variability is higher than that for farm and laboratory mammals. In the present study, our previously published approach considering the use of energy metabolism and the link between energy and organic matter turnover rate at the whole body and organ

Modelling 3H and 14C transfer to farm animals and their products under steady state conditions

International Nuclear Information System (INIS)

Galeriu, D.; Melintescu, A.; Beresford, N.A.; Crout, N.M.J.; Peterson, R.; Takeda, H.

2007-01-01

The radionuclides 14 C and 3 H may both be released from nuclear facilities. These radionuclides are unusual, in that they are isotopes of macro-elements which form the basis of animal tissues, feed and, in the case of 3 H, water. There are few published values describing the transfer of 3 H and 14 C from feed to animal derived food products under steady state conditions. Approaches are described which enable the prediction of 14 C and 3 H transfer parameter values from readily available information on the stable H or C concentration of animal feeds, tissues and milk, water turnover rates, and feed intakes and digestibilities. We recommend that the concentration ratio between feed and animal product activity concentrations be used as it is less variable than the transfer coefficient (ratio between radionuclide activity concentration in animal milk or tissue to the daily intake of a radionuclide)

Transfer time estimation of 129I, 99Tc and 14C in the geological layers of the Saligny site

International Nuclear Information System (INIS)

Dogaru, Daniela; Niculae, Ortenzia; Terente, M.; Jinescu, Gh.; Duliu, O.G.

2009-01-01

The paper describes the assessment of transfer time of 129 I, 99 Tc and 14 C in the geological layers of Saligny site, selected as Near Surface Final Repository for short-lived low and intermediate level radioactive waste generated by the operation and decommissioning of the four units of Cernavoda NPP equipped with the CANDU-6 Canadian type reactors. The geological aspects of Saligny site are presented for which the transfer time of radio-nuclides is necessary to assess. The conceptual model of the repository as well as the associated mathematical model which describes the transfer of radio-nuclides from radioactive waste disposal system to aquifer is also presented in the paper. The transfer time of these radionuclides is derived from the time difference when a radionuclide reaches the highest peak value of concentration into two adjacent compartments. The transfer time is compared with the half-life of radio-nuclides in order to asses the role of geological layers of the site in delaying the transfer of radio-nuclides. The evaluation was performed using the AMBER computing code. also a comparison with results from HYDRUS computer code is done. (authors)

Crystal structure, quantum mechanical investigation, IR and NMR spectroscopy of two new organic salts: (C8H12NO)·[NO3] (I) and (C8H14N4)·[ClO4]2 (II)

Science.gov (United States)

Bayar, I.; Khedhiri, L.; Soudani, S.; Lefebvre, F.; Pereira da Silva, P. S.; Ben Nasr, C.

2018-06-01

Two new organic-inorganic hybrid materials, 4-methoxybenzylammonium nitrate, (C8H12NO)·[NO3] (I), and 2-(1-piperazinyl)pyrimidinium bis(perchlorate), (C8H14N4)·[ClO4]2(II), have been synthesized by an acid/base reaction at room temperature, their structures were determined by single crystal X-ray diffraction. Compound (I) crystallizes in the orthorhombic system and Pnma space group with a = 15.7908 (7), b = 6.8032 (3), c = 8.7091 (4) Å, V = 935.60 (7) Å3 with Z = 4. Full-matrix least-squares refinement converged at R = 0.038 and wR(F2) = 0.115. Compound (II) belongs to the monoclinic system, space group P21/c with the following parameters: a = 10.798(2), b = 7.330(1), c = 21.186(2) Å, β = 120.641 (4)°, V = 1442.7 (3) Å3and Z = 4. The structure was refined to R = 0.044, wR(F2) = 0.132. In the structures of (I) and (II), the anionic and cationic entities are interconnected by hydrogen bonding contacts forming three-dimensional networks. Intermolecular interactions were investigated by Hirshfeld surfaces and the contacts of the four different chloride atoms in (II) were compared. The Molecular Electrostatic Potential (MEP) maps and the HOMO and LUMO energy gaps of both compounds were computed. The vibrational absorption bands were identified by infrared spectroscopy. These compounds were also investigated by solid-state 13C, 35Cl and 15N NMR spectroscopy. DFT calculations allowed the attribution of the IR and NMR bands.

A convenient method for 14C-labeling of 2-methylthio-1-[4-N-α-ethoxycarbonylbenzyl)-amino-benzyl] -5-hydroxymethyl-2-[14C]-1H-imidazole and 1-[4-N-α-ethoxy-carbonylbenzyl)-aminobenzyl]-5-hydroxymethyl-2-[14C] -1H-imidazole as potential antihypertensives

International Nuclear Information System (INIS)

Nader Saemian; Gholamhossein Shirvani; Mohsen Javaheri; Sayed Sajad Oliyaee

2012-01-01

The key synthetic intermediate, (2-mercapto-1-(4-nitrobenzyl)-1H-imidazol-5-yl)methanol-[2- 14 C], has been synthesized by using one pot procedure from potassium[ 14 C]-thiocyanate. It was converted to two nonpeptide angiotensin II receptor antagonists, 2-methylthio-1-[4-N-α-ethoxycarbonyl benzyl)-aminobenzyl]-5-hydroxymethyl-1H-imidazole-[2- 14 C] and 1-[4-N-α-ethoxy-carbonylbenzyl)-aminobenzyl] -5-hydroxymethyl-1H-imidazole-[2- 14 C] via a 3-step sequence synthetic pathway. (author)

The synthesis of the 2H, 3H, and 14C-isotopomers of 2'-deoxy-2',2'-difluorocytidine hydrochloride, an anti-tumor compound

International Nuclear Information System (INIS)

Wheeler, W.J.; Mabry, T.E.; Jones, C.D.

1991-01-01

The 2 H, 3 H, and 14 C-isotopomers of 2'-deoxy-2', 2'-difluorocytidine hydrochloride (gemcitabine hydrochloride) have been synthesized in two radiochemical steps from the reaction of bis-trimethylsilylcytosine-[2- 14 C] and 3,5-O-bis-benzoyl-1-O-methanesulfonyl-2-deoxy-2,2-difluororibose. A mixture of anomers of 3',5'-dibenzoyl-2'-deoxy-2',2'-difluorocytidine or its 14 C-isotopomer were obtained which were readily separated by crystallization from ethyl acetate. Deprotection using methanolic ammonia yielded the target compound. The 2 H and 3 H-isotopomers were prepared by deuterium (or tritium) gas hydrogenolysis of 5-iodo-2'-deoxy-2',2'-difluorocytidine. (author)

Reduced permeation of 14C-sucrose, 3H-mannitol and 3H-inulin across blood-brain barrier in nephrectomized rats

International Nuclear Information System (INIS)

Preston, E.; Haas, N.; Allen, M.

1984-01-01

Experiments were carried out to determine if changes in the concentration-time profile of a blood-borne radiotracer such as 14 C-sucrose would spuriously alter measurements of its permeation across the blood-brain barrier (permeability-area product, PA) based on a 2-compartment (plasma/brain) simple diffusion model. Anesthetized rats which were bilaterally nephrectomized and given a standard intravenous bolus injection of 14 C-sucrose, 3 H-mannitol or 3 H-inulin exhibited an elevated plasma tracer concentration compared to control animals. However, tracer concentration measured in brain parenchyma after 30 min was not proportionally elevated, and PA calculated from the ratio, parenchymal tracer concentration: plasma concentration-time integral, was significantly reduced below control values. In control rats, distortion and elevation of the plasma 14 C-sucrose profile by continuous intravenous infusion did not result in lowered PA values. This suggested that the lowering of PA by nephrectomy reflected reduced cerebrovascular permeability or area or other cerebral influence rather than a deficiency in the 2-compartment model for PA measurement

Methods of I-129 analysis for environmental monitoring

International Nuclear Information System (INIS)

Nomura, T.; Katagiri, H.; Kitahara, Y.; Fukuda, S.

1980-01-01

Among the radioiodine isotopes discharged from nuclear facilities, I-129 has the longest half-life (1.7 x 10 7 years) and thus environmental monitoring of this nuclide is important. Methods of analysis of low level I-129 in environmental samples such as milk, crops, seaweeds and soils are described. The iodine is separated from the dried or pulverized samples by ignition at 1000 0 C in a quartz combustion apparatus with a stream of oxygen. Stable I-127 is simultaneously determined and the atom ratio of 129 I/ 127 I calculated in order to evaluate the thyroid dose by the specific activity method. Results of an analysis of typical food samples collected near the fuel reprocessing plant of Tokai Works showed no I-129 concentrations higher than the detection limit of the method (10 -2 pCi for 10 g. dry sample). (UK)

Experiences with liquid scintillation counting of 3H, 14C and 35S from plant material

International Nuclear Information System (INIS)

Das, S.K.

1974-01-01

Relative merits of different methods in radioassay of three soft beta emitting isotopes like 3 H, 14 C and 35 S from plant material have been assessed. The methods used are: (1) combustion method (2) use of tissue solubilizing agents and (3) wet digestion method. Results show that determinations of 14 C by combustion method; 3 H by combustion and Mahin and Lofberg's method; and 35 S by wet digestion method are superior for plant material than the other methods tried. (author)

Uptake of [3H]PAH and [14C]urate into isolated proximal tubular segments of the pig kidney

International Nuclear Information System (INIS)

Schali, C.; Roch-Ramel, F.

1981-01-01

Segments of proximal convoluted (PCT) and proximal straight (PST) tubules of minipigs and normal-sized pigs were microdissected (without collagenase treatment) and incubated (30 min, 37 0 C, pH 7.4) in Ringer solution (under O 2 ) containing [ 3 H]PAH (3.10 -5 M) or [ 14 C]urate (9.10 -5 M) and, in inhibitor studies, probenecid, pyrazinoic acid (PZA), urate, or PAH, all at 1 mM. In both strains the uptake of [ 3 H]PAH expressed as mean T/M ratio (cpm per ml tissue water/cpm per ml incubation medium) was significantly higher (P 14 C]urate. In eight minipigs the T/M was 4.9 +/- 0.5 in 24 PCT and 2 +/- 0.2 in 25 PST. In normal-sized pigs the T/M was 3.8 +/- 0.3 in 35 PCT (five pigs) and 1.9 +/- 0.4 in eight PST (two pigs). In inhibitor studies urate significantly depressed the uptake of [ 3 H]PAH, and unlabeled PAH depressed the uptake of [ 14 C]urate. PZA significantly inhibited the uptake of [ 14 C]urate but not that of [ 3 H]PAH, whereas probenecid had a strong inhibitory efect on the uptake of both compounds. These results suggest that [ 14 C]urate and [ 3 H]PAH are transported by a transport system located mainly in the proximal convoluted tubule. These findings are in contrast in the findings are in contrast to the findings obtained in rabbits in which the transport system of PAH and urate is mainly located in the proximal part of the pars recta

Specific activity of 129I in environmental samples

International Nuclear Information System (INIS)

Ravi, P.M.; Iyer, M.R.; Bhat, I.S.; Somasundaram, S.; Subramanian, M.S.

1988-01-01

129 I finds its way into the environment as a result of man-made nuclear operations. It is also formed by the interaction of cosmic rays with xenon isotopes and spontaneous fission of naturally occurring uranium. 129 I and stable 127 I contents of thyroid, milk, seaweed and aplysia cell samples collected from around a fuel reprocessing plant were estimated by neutron activation analysis method. The annual 129 I intake of an individual works out to be about 0.3 Bq as compared to the natural radioactivity content in human body of about 5000 Bq. (author). 3 tabs

Electro-removal of H-3 and C-14 contained in scintillation liquid absorbed in soils type Phaeozem; Electrorremocion de H-3 y C-14 contenidos en liquido de centelleo absorbidos en suelos tipo Phaeozem

Energy Technology Data Exchange (ETDEWEB)

Valdovinos, V.; Bustos, E. [Centro de Investigacion y Desarrollo Tecnologico en Electroquimica, Parque Tecnologico Queretaro s/n, San Fandila, 76703 Pedro Escobedo, Queretaro (Mexico); Monroy G, F., E-mail: vvaldovinos@cideteq.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

2014-10-15

This paper presents the results of electro-removal, an electrochemical treatment in soils contaminated with H-3 and C-14 contained in scintillation liquids absorbed in soils. For this purpose the best electrochemical conditions were used, which are: scintillation liquid Ultima Gold Xr, water (1:1) and 1 m A in the passage of current. The media were characterized before and after of applying the different potentials by various analytical techniques, such as: liquids by gas chromatography with a flame ionization detector, solids and liquids by Fourier transform infrared spectroscopy (Ftir) and electrodes by scanning electron microscopy with elemental analysis by energy-dispersive X-ray spectroscopy. Later standard samples with H-3 and C-14 were prepared and the electrochemical treatment was applied to previously established conditions. After electrochemical treatment the scintillation liquid characterization was performed by gas chromatography and a scintillation counter to see the disintegrations per minute. According to results of Ftir, soils show no deterioration and in the liquid phase the amount of water increases as the applied potential, due to oxidation-reduction reactions where happen modification or mineralization of organic molecules (H{sub 2}O and CO{sub 2} formation). In 4 h of treatment, removal percentages in the liquid phase, were: 53.6% of H-3 and 11.6% of C-14. (Author)

Structural and electrical phase transitions in the [(C2H5)4N]2ZnI3.86Cl0.14 system

Science.gov (United States)

Rhouma, Najla Mahbouli; Rayes, Ali; Mezzadri, Francesco; Delmonte, Davide; Cabassi, Riccardo; Calestani, Gianluca; Loukil, Mohamed

2017-12-01

The organic-inorganic hybrid non-centrosymmetric material [(C2H5)4N]2ZnI3.86Cl0.14 has been studied by X-ray diffraction (XRD), differential scanning calorimetry (DSC), dielectric and transport measurements. In analogy with the corresponding tetraiodo-zincate analogue, the material crystallizes at room temperature in the tetragonal system, space group P 4 ̅ 21m (No. 113), with lattice parameters a = 13.743(6) and c = 14.785(10) Å. DSC and XRD characterizations pointed out the occurrence of two phases transitions, one of second order at about 290 K and the other of the first order at T = 451 K. The former is related to an electrical transition from insulating to thermally activated transport mechanism displaying clear hints of ionic conduction, the latter leads to a phase showing the typical features of plastic crystals in its powder XRD pattern. The pattern was indexed by an orthorhombic cell, a = 15.724(1), b = 17.907(1) and c = 10.585(1) Å, and a reliable model was found and refined in the Pna21 space group. The model consists of ordered tetrahedral ZnCl42- units intercalated by fully disordered tetraethylammonium cations.

Metabolism of high density lipoproteins reconstituted with [3H]cholesteryl ester and [14C]cholesterol in the rat, with special reference to the ovary

International Nuclear Information System (INIS)

Nestler, J.E.; Bamberger, M.; Rothblat, G.H.; Strauss, J.F. III

1985-01-01

In order to study the metabolism of high density lipoprotein (HDL)-carried sterol in the rat, human HDL was reconstituted with [ 14 C]cholesterol and [ 3 H]cholesteryl ester. After iv injection into immature PMSG-human CG primed rats pretreated with 4-aminopyrazolopyrimidine and aminoglutethimide, there was time-dependent accumulation of 3 H and 14 C in various organs which reached a maximum by 15-90 min. On a milligram wet weight basis, uptake of 3 H and 14 C was greatest in the adrenals, next in ovaries, followed by the liver, with little uptake by kidneys and spleen. On an organ basis, accumulation was greatest by the liver. Coadministration of excess unlabeled HDL, but not human low density lipoprotein, reduced accumulation of radioactivity by the ovaries and adrenals by 60%, indicating a specific and saturable uptake process. Granulosa cells cultured in lipoprotein-deficient medium with reconstituted HDL formed 3 H- and 14 C-labeled 20 alpha-hydroxypregn-4-en-3-one. Over a 24-h period, utilization of both [ 14 C]cholesterol and [ 3 H]cholesteryl ester was linear, but rates of utilization of the two sterol moieties were not parallel. Lysosomotropic agents had no effect on utilization of either free or esterified cholesterol for steroidogenesis but reduced degradation of 125 I-labeled low density lipoprotein apoprotein. These findings lend further support to the concept of a distinct HDL pathway in steroidogenic cells of the rat

Measuring techniques for environmental sup 3 H, sup 14 C and sup 222 Rn by liquid scintillation counter

Energy Technology Data Exchange (ETDEWEB)

Takata, Shigeru; Saito, Masaaki (Tokyo Metropolitan Isotope Research Center (Japan))

1991-02-01

Measuring techniques for environmental {sup 3}H, {sup 14}C and {sup 222}Rn with a liquid scintillation counter have been studied. {sup 3}H in environmental water was enriched by electrolysis and measured with a low background liquid scintillation counter. By this technique, {sup 3}H concentration of ground water, river water, sea water and rain water at Tokyo was founded to be 0.1 {approx} 2.5 Bq/1. {sup 14}C in taurine and ethyl-alcohol was measured directly liquid scintillation counter. By this {sup 14}C measuring, natural products, contain low level {sup 14}C, were distinguished from synthesised products contain no {sup 14}C. {sup 222}Rn in toluene extracted from environmental water or air was measured by scintillation pulse interval analysis method. By this technique, {sup 222}Rn was able to be measured under very low background counting rate, 0.03cpm, and high efficiency. (author).

Accurate determination of 129I concentrations and 129I/137Cs ratios in spent nuclear resins by Accelerator Mass Spectrometry

International Nuclear Information System (INIS)

Nottoli, Emmanuelle; Bienvenu, Philippe; Labet, Alexandre; Bourlès, Didier; Arnold, Maurice; Bertaux, Maité

2014-01-01

Determining long-lived radionuclide concentrations in radioactive waste has fundamental implications for the long-term management of storage sites. This paper focuses on the measurement of low 129 I contents in ion exchange resins used for primary fluid purification in Pressurised Water Reactors (PWR). Iodine-129 concentrations were successfully determined using Accelerator Mass Spectrometry (AMS) following a chemical procedure which included (1) acid digestion of resin samples in HNO 3 /HClO 4 , (2) radioactive decontamination by selective iodine extraction using a new chromatographic resin (CL Resin), and (3) AgI precipitation. Measured 129 I concentrations ranged from 4 to 12 ng/g, i.e. from 0.03 to 0.08 Bq/g. The calculation of 129 I/ 137 Cs activity ratios used for routine waste management produced values in agreement with the few available data for PWR resin samples. - Highlights: • In the context of radioactive waste management, this study aimed at measuring 129 I in spent resins using accelerator mass spectrometry. • The treatment procedure included microwave acid digestion of samples, iodine extraction by CL resins and AgI precipitation. • Developed first on synthetic matrices, the chemical treatment procedure was then successfully applied to real resin samples. • 129 I concentrations ranged from 4 to 12 ng/g of dry resin. • Results are in agreement with previous measurements and support reference values currently used for nuclear resin management

Analysis of {sup 14}CO{sub 2} trapped {sup 14}C Sorbent, and {sup 14}C and {sup 3}H Radioactivity Determination in Resins and Oils from Nuclear Power Plants Using a Combustion Method

Energy Technology Data Exchange (ETDEWEB)

Ko, Young Gun; Kim, Chang Jong; Choi, Geun Sik; Chung, Kun Ho; Kang, Mun Ja [KAERI, Daejeon (Korea, Republic of)

2016-05-15

Tritium ({sup 3}H, T) generated in the heavy water and C fourteen ({sup 14}C) originated from the graphite moderator or structural materials of the nuclear power plant can cause acute and/or chronic harmful effects by inhalation and ingestion of these radionuclides owing to their binding affinity toward biomolecules and gas phase. {sup 3}H and {sup 14}C radioactivity in ion exchange resins and oils from nuclear power plants were determined by an oxidation (combustion) method. The 0.1 M HNO{sub 3} solution and the {sup 14}C sorbent trapped the {sub 3}H and {sup 14}C respectively in the gas from the combustion of samples. All samples were burned without ash in the combustion system. The reaction of CO{sub 2} and {sup 14}C sorbent was investigated by FT-IR analysis. The study demonstrated the different reaction mechanism according to the CO{sub 2} concentration. In the FT-IR study, it is clearly confirmed that CO{sub 2} from the burned 1 g of sample can be trapped in the {sup 14}C sorbent completely. During the reaction of CO{sub 2} and {sup 14}C sorbent, the temperature and the viscosity of {sup 14}C sorbent increased due to the decrease of enthalpy change and the bonding between each molecules of the sorbent. We expect that our FT-IR study could motivate the development of {sup 14}C sorbent and confirm the {sup 14}C trapping performance of the {sup 14}C sorbent.

Estimation of 129I inventory in the oceans

International Nuclear Information System (INIS)

Xuegao Chen; Xue Liu; Peng Yi; Zhongbo Yu; Hohai University, Nanjing; Ala Aldahan; Uppsala University, Uppsala; Li Chen; Desert Research Institute, Las Vegas, NV; Goran Possnert

2016-01-01

Spatial distribution of oceanic 129 I inventory presented here is based on collection of data from published literatures coupled with model calculation using ArcGIS software tools. A total of 363 thiessen polygons were created for the oceans in order to cover the tremendous variability in distribution of 129 I data range. The results indicate that total 129 I oceanic inventory is approximately 7310 kg, which is mainly stored in the region of the North Atlantic and the Arctic Oceans. The concentrations of 129 I in the oceans are 3-4 orders of magnitude higher than the pre-anthropogenic level reflecting effects of post 1945 anthropogenic activities. (author)

Optimisation of the measurement protocols of 129I and 129I/127I. Methodology establishment for the measurement in environmental matrices

International Nuclear Information System (INIS)

Frechou, C.

2000-01-01

129 I, is a natural long-lived isotope, with a half-life of 15,7 million years, also artificially produced in nuclear power plant. It is then released in the liquid and gaseous effluents of the nuclear fuel reprocessing plants. 129 I is integrated in all biological compartments at different activity levels, depending on their distance from the emission source and their ability to metabolize iodine. Performances of the different 129 I and 129 I/ 127 I measurement techniques available: Radiochemical Neutron Activation Analysis, Accelerator Mass Spectrometry, direct γ-X spectrometry and liquid scintillation were evaluated. Associated radiochemical preparation steps of the two first techniques were optimized and adapted to the characteristics of the major environmental matrices. In a first step, the radiochemical protocols were developed and validated. In a second step, intercomparison exercises have been lead on various environmental samples presenting different 129 I activity levels. They showed the good agreement between the results given by the three techniques on different environmental matrices with activities between 0,2 and 200 Bq.kg -1 dry weight. As a conclusion, a methodology for the measurement of 129 I and 129 I/ 127 I ratio in environmental samples is proposed. It includes a decisional diagram taking into account the characteristics of the matrices, the detection limits and the answer delay. A study on the losses of 129 I during the calcination of an algae was lead by direct γ-X spectrometry and application studies were made to measure 129 I levels in different biological compartments issued from various locations: 129 I activity interspecific variation in different species of seaweeds from the French channel coast under the relative influence of La Hague, 129 I levels in bovine thyroids from the Cotentin area and 129 I in vegetal samples collected around the nuclear reprocessing plant of Marcoule. (author)

DETERMINATION OF THE 129I IN PRIMARY COOLANT OF PWR

Directory of Open Access Journals (Sweden)

KE CHON CHOI

2013-02-01

In this report, the effect of the boron content in a pressurized-water reactor primary coolant on the separation process of 129I was examined, as was the effect of 3H on the measurement of the activity of iodine. As a result, no influence of the boron content and of the simultaneous 3H presence was found with activity concentrations of 3H lower than 50 Bq/mL, and with a boron concentration of less than 2,000 μg/mL.

{sup 127}I and {sup 129}I/{sup 127}I isotopic ratio in marine alga Fucus virsoides from the North Adriatic Sea

Energy Technology Data Exchange (ETDEWEB)

Osterc, Andrej [Department of Environmental Sciences, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Stibilj, Vekoslava [Department of Environmental Sciences, Jozef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)], E-mail: vekoslava.stibilj@ijs.si

2008-04-15

The only stable iodine isotope is {sup 127}I and the natural {sup 129}I/{sup 127}I ratio in the biosphere has increased from 10{sup -15}-10{sup -14} to 10{sup -10}-10{sup -9}, mainly due to emissions from nuclear fuel reprocessing plants. In Europe they are located at La Hague (France) and Sellafield (England), where the ratio of {sup 129}I/{sup 127}I is up to 10{sup -4}. The marine environment, i.e. the oceans, is the major source of iodine with average concentrations of around 60 {mu}g L{sup -1} iodine in seawater. Brown algae accumulate iodine at high levels of up to 1.0% of dry weight, and therefore they are an ideal bioindicator for studying the levels of {sup 127}I and {sup 129}I in the marine environment. A radiochemical neutron activation analysis (RNAA) method, developed at our laboratory, was used for {sup 129}I determination in the brown alga Fucus virsoides (Donati) J. Agardh, and the same technique of RNAA was used for total {sup 127}I determination. The samples were collected along the coast of the Gulf of Trieste and the West coast of Istria in the North Adriatic Sea in the period from 2005 to 2006. Values of the {sup 129}I/{sup 127}I ratio up to 10{sup -9} were found, which is in agreement with the present average global distribution of {sup 129}I. The levels of stable iodine found were in the range from 235 to 506 {mu}g g{sup -1} and the levels of {sup 129}I from 1.7 to 7.3 x 10{sup -3} Bq kg{sup -1} (2.6-10.9 x 10{sup -7} {mu}g g{sup -1}), on a dry matter basis.

Synthesis of 14C- and 3H-labelled 4-(4-nitrophenyl)aminophenylisothiocyanate (Go 9333/CGP 4540; amoscanate)

International Nuclear Information System (INIS)

Anjaneyulu, B.; Maller, R.K.; Nagarajan, K.

1985-01-01

Amoscanate, a broad spectrum anthelmintic, labelled with carbon-14 on the isothiocyanate carbon atom was prepared in an overall yield of 13% at a specific activity of 4.13 μCi/mg from potassium [ 14 C]thiocyanate. The 4-nitro[U- 14 C]phenyl ring labelled compound was synthesized in 20.4% overall yield from [U- 14 C]aniline at a specific activity of 12.2 μCi/mg. The corresponding tritiated compound was prepared from 4-amino[2- 3 H]acetanilide at 112 μCi/mg. Labelling with tritium in the aromatic ring bearing the isothiocyanate group was achieved by catalysed halogen-tritium replacement. However, for pharmacokinetic and metabolism studies in experimental animals, the 14 C- and 3 H-labels associated with the phenylisothiocyanate moiety subsequently proved disadvantageous because of the instability of the labels in vivo. (author)

Measurement of reaction cross sections of {sup 129}I induced by DT neutrons

Energy Technology Data Exchange (ETDEWEB)

Nakano, Daisuke; Murata, Isao; Takahashi, Akito [Osaka Univ., Suita (Japan). Faculty of Engineering

1997-03-01

The cross sections were measured for the {sup 129}I(n,2n){sup 128}I and {sup 129}I(n,{gamma}){sup 130}I reactions by DT neutrons, at OKTAVIAN facility of Osaka University, Japan. The foil activation method was used in the measurement. The sample was a sealed source of {sup 129}I, which was covered with a Cd foil. The irradiations were performed for 75 minutes to obtain the cross section of reaction producing {sup 128}I (T{sub 1/2}=24.99m) and 22 hours for the {sup 130}I (T{sub 1/2}=12.36h), respectively. The gamma-rays emitted from the irradiated sample were measured with a high purity Ge detector. The measured cross sections of {sup 129}I(n,2n){sup 128}I and {sup 129}I(n,{gamma}){sup 130}I reactions were 0.92{+-}0.11 barn and 0.013{+-}0.002 barn, respectively. For the {sup 129}I(n,2n){sup 128}I reaction, the evaluation of JENDL-3.2 overestimates cross section about 60% to the experimental result. However, especially for the {sup 129}I(n,{gamma}) reaction, the measured cross section may include the contribution from the neutrons in MeV region as well as epithermal ones. Also, the obtained cross section of the {sup 129}I(n,{gamma}){sup 130}I reaction was evaluated as an effective production cross section of {sup 130}I including {sup 129}I(n,{gamma}){sup 130m}I reaction. In order to remove the contribution from the epithermal and MeV region neutrons. A new method was proposed for the measurement of (n,{gamma}) reaction cross section. (author)

14 CFR 129.113 - Fuel tank system maintenance program.

Science.gov (United States)

2010-01-01

... 14 Aeronautics and Space 3 2010-01-01 2010-01-01 false Fuel tank system maintenance program. 129... Continued Airworthiness and Safety Improvements § 129.113 Fuel tank system maintenance program. (a) Except... on which an auxiliary fuel tank is installed under a field approval, before June 16, 2008, the...

14 CFR 129.19 - Air traffic rules and procedures.

Science.gov (United States)

2010-01-01

... 14 Aeronautics and Space 3 2010-01-01 2010-01-01 false Air traffic rules and procedures. 129.19 Section 129.19 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR CARRIERS AND OPERATORS FOR COMPENSATION OR HIRE: CERTIFICATION AND OPERATIONS OPERATIONS: FOREIGN AIR CARRIERS AND FOREIGN OPERATORS OF ...

Synthesis of /sup 14/C- and /sup 3/H-labeled fluoxetine, a selective serotonin uptake inhibitor

Energy Technology Data Exchange (ETDEWEB)

Robertson, D.W.; Krushinski, J.H.; Wong, D.T.; Kau, D.

1987-11-01

Fluoxetine (N-methyl-..gamma..-(4-(trifluoromethyl)phenoxy) benzenepropanamine) is a potent, highly selective serotonin uptake inhibitor that is useful in treating a variety of major psychiatric derangements. We have synthesized this compound in /sup 14/C- and /sup 3/H-labeled forms. The tritium label was introduced in the final step by catalytic dehalogenation of the brominated fluoxetine precursor. Reaction conditions could be controlled such that catalytic hydrogenolysis of the labile C-O benzylic bond was minimized. Following HPLC purification, (/sup 3/H)-fluoxetine was obtained in a state of high radiochemical purity (98%) and specific activity (20.4 Ci/mmol). The /sup 14/C-label was introduced in the final step via a nucleophilic aromatic substitution reaction between the sodium salt of ..cap alpha..-(2-(methylamino)ethyl)benzenemethanol and uniformly ring-labeled p-chlorobenzotrifluoride. Following purification by flash chromatography, (/sup 14/C)-fluoxetine was obtained in 98.3% radiochemical purity with a specific activity of 5.52 mCi/mmol.

Synthesis of 14C- and 2H-labeled 1,3 dihydro-3, 3-dimethyl-5-(1,4,5,6,- tetrahydro-6-oxo-3-pyridazinyl)-2H-indol-2-one (LY195115), an orally effective positive inotrope

International Nuclear Information System (INIS)

Robertson, D.W.; Krushinski, J.H.; Kau, D.

1986-01-01

The synthesis of 14 C- and 2 H-labeled 1,3-dihydro-3,3-dimethyl-5-(1,4,5,6-tetrahydro-6-oxo-3-pyridazinyl)-2H-indol -2-one (LY195115), an extremely potent, orally-effective cardiotonic with inotropic and vasodilator activities is described. The 14 C-label was introduced in the antepenultimate step by reaction of a β-chloroketone precursor with Na 14 CN; acid-catalyzed hydrolysis and cyclization with hydrazine provided the tetrahydropyridazinone bearing the 14 C-label in the oxo-carbon. 1,3-Dihydro-3,3-di(methyl-d 3 ) -2H-indol-2-one was prepared by exhaustive methylation of 1-acetyl-1,3-dihydro-2H-indol-2-one with sodium hydride and iodomethane-d 3 , followed by removal of the nitrogen protecting group. This labeled material was converted in two steps to [ 2 H 6 ]-LY195115. (author)

Environmental concentration and migration of 129I

International Nuclear Information System (INIS)

Brauer, F.P.; Strebin, R.S. Jr.

1982-01-01

Local sources of 129 I suitable for study of migration in the environment are uranium ore bodies for long periods and nuclear fuel reprocessing operations for recent periods. Uranium ores produce 129 I from spontaneous and neutron-induced fission. Nuclear fuel reprocessing has resulted in releases of 129 I to both the atmosphere and the hydrosphere. The long-term fate of surface-deposited and groundwater 129 I was studied. Neutron activation analysis was used to measure the low levels of 129 I and natural 127 I in samples near and remote from nuclear fuel reprocessing facilities. Measurements were made on air samples, vegetation, soil, surface water, groundwater and uranium ore samples. Samples were collected both during reprocessing operations and after reprocessing activities had been discontinued for several years. The 129 I was found to accumulate in the top soil and litter layer. The surface concentrations of 129 I in forest communities were found to be several times higher than for nearby grass communities. The 129 I levels were found to persist in the environment after reprocessing activities had been discontinued. Measurable 129 I was found to be contained in uranium ore samples from a variety of locations and with a range of uranium concentrations. Thus ore bodies constitute a source of 129 I suitable for study of migration over long periods. Iodine-129 has entered surface and groundwater as the result of liquid and atmospheric discharges from nuclear fuel reprocessing facilities. The iodine in water samples was found to be anionic and travel with the water flow. Thus 129 I was found to provide high sensitivity for hydrology tracer studies and radioactivity migration surveillance. Once 129 I enters the hydrosphere it migrates with the water with little or no hold-up by exchange with cationic exchangers such as soil or silt

Isotope effects and their implications for the covalent binding of inhaled [3H]- and [14C]formaldehyde in the rat nasal mucosa

International Nuclear Information System (INIS)

Heck Hd'; Casanova, M.

1987-01-01

DNA-protein crosslinks were formed in the nasal respiratory mucosa of Fischer-344 rats exposed for 3 hr to selected concentrations of [ 3 H]- and [ 14 C]formaldehyde ( 3 HCHO and H 14 CHO). In rats depleted of glutathione (GSH) and exposed to 10 ppm of 3 HCHO and H 14 CHO, the 3 H/ 14 C ratio of the fraction of the DNA that was crosslinked to proteins was significantly (39 +/- 6%) higher than that of the inhaled gas. This suggests an isotope effect, either on the formation of DNA-protein crosslinks by labeled HCHO or on the oxidation of labeled HCHO catalyzed by formaldehyde (FDH) or aldehyde dehydrogenase (AldDH). The possibility of an isotope effect on the formation of crosslinks was investigated using rat hepatic nuclei incubated with [ 3 H]- and [ 14 C]formaldehyde (0.1 mM, 37 degrees C). A small (3.4 +/- 0.9%) isotope effect was detected on this reaction, which slightly favored 3 HCHO over H 14 CHO in binding to DNA. The magnitude of this isotope effect cannot account for the high isotope ratio observed in the crosslinked DNA in vivo. The possibility of an isotope effect on the oxidation of 3 HCHO and H 14 CHO catalyzed by FDH was investigated using homogenates of the rat nasal mucosa incubated with [ 3 H]- and [ 14 C]formaldehyde at total formaldehyde concentrations ranging from 0.1 to 11 microM, NAD+ (1 mM), GSH (15 mM), and pyrazole (1 mM). The experiments showed that 3 HCHO is oxidized significantly more slowly than H 14 CHO under these conditions (Vmax/Km (H 14 CHO) divided by Vmax/Km ( 3 HCHO) = 1.82 +/- 0.11). A similar isotope effect was observed in the absence of GSH, presumably due to the oxidation of 3 HCHO and H 14 CHO catalyzed by AldDH

Neutron activation analysis of 127I and 129I environmental samples

International Nuclear Information System (INIS)

Takeishi, Minoru; Namiki, Atsushi; Ishida, Junichiro; Iwai, Makoto

1987-01-01

The analytical method of 127 I and 129 I in environmental samples has been studied and the background levels of these nuclides in soils, seaweeds and milk were measured. The analytical method consists of the combustion technique and neutron activation analysis (N.A.A.). The iodine was separated from samples by ignition at about 1,000 deg C in a quartz combustion apparatus with an oxygen and a nitrogen stream, and was absorbed by small amounts of active charcoal. The iodine was then purified through the carbontetrachloride extraction method and the PdI 2 decomposition method. Irradiation was conducted by JRR-4 (n th : 8 x 10 13 n/cm 2 · sec) for 40 min. After irradiation, the iodine was purified by the solvent extraction method same as pre-irradiation extraction. Each activity of 126 I and 130 I, which was produced by 127 I(n,2n) 126 I and 129 I(n,γ) 130 I reaction respectively, was measured by γ-spectrometry using a Ge-detector. The lower detection limits of 129 I by this method were 4 x 10 -7 Bq/g for dry soil, 7 x 10 -8 Bq/g for fresh seaweeds and 7 x 10 -6 Bq/l for fresh milk, respectively. The relative standard deviation of 129 I measurements in soil and milk were less than 10 %. (author)

The seasonal fluctuations and accumulation of iodine-129 in relation to the hydrogeochemistry of the Wolf Creek Research Basin, a discontinuous permafrost watershed

Energy Technology Data Exchange (ETDEWEB)

Herod, Matthew N., E-mail: mattherod@gmail.com [André Lalonde AMS Lab, Department of Earth and Environmental Science, University of Ottawa, 25 Templeton St., Ottawa, ON K1N 6N5 (Canada); Li, Tianjiao [André Lalonde AMS Lab, Department of Earth and Environmental Science, University of Ottawa, 25 Templeton St., Ottawa, ON K1N 6N5 (Canada); Pellerin, André [Center for Geomicrobiology, Department of Bioscience, Aarhus University, Ny Munkegade 116, 8000 Aarhus C (Denmark); Kieser, William E.; Clark, Ian D. [André Lalonde AMS Lab, Department of Earth and Environmental Science, University of Ottawa, 25 Templeton St., Ottawa, ON K1N 6N5 (Canada)

2016-11-01

suggesting that {sup 129}I is a promising hydrologic tracer, particularly when used in concert with other stable and radioisotopes. - Highlights: • {sup 129}I behaviour, storage and transport within a watershed are poorly understood. • This is a study of {sup 129}I sources and partitioning in watershed reservoirs over time. • A variety of geochemical and isotope tracers revealed temporal changes in flowpaths. • 88% of the annual {sup 129}I input is stored in organic soils. • {sup 129}I is accumulating and is a useful tracer coupled with {sup 14}C, {sup 3}H and stable isotopes.

1,4-Dimethyl-3-phenyl-3H-pyrazolo[3,4-c]isoquinolin-5(4H-one

Directory of Open Access Journals (Sweden)

Giuseppe Daidone

2008-05-01

Full Text Available The title compound, C18H15N3O, is the product of the thermal decomposition of the diazonium salt derived from 2-amino-N-methyl-N-(3-methyl-1-phenyl-1H-pyrazol-5-ylbenzamide. It is characterized by a trans orientation of the methyl groups with respect to the tricyclic ring system. The molecule has a nearly planar phenylpyrazolo[3,4-c]isoquinolin-5-one system, the largest deviation from the mean plane being 0.066 (2 Å for the O atom. The dihedral angle between the phenyl substituent and the heterotricycle is 67 (1°. The packing is stabilized by C—H...N hydrogen-bond interactions, with the formation of molecular chains along the c axis.

Photodissociation of pyrene cations: structure and energetics from C16H10(+) to C14(+) and almost everything in between.

Science.gov (United States)

West, Brandi; Useli-Bacchitta, Francesca; Sabbah, Hassan; Blanchet, Valérie; Bodi, Andras; Mayer, Paul M; Joblin, Christine

2014-09-11

The unimolecular dissociation of the pyrene radical cation, C16H10(+•), has been explored using a combination of computational techniques and experimental approaches, such as multiple photon absorption in the cold ion trap Piège à Ions pour la Recherche et l'Etude de Nouvelles Espèces Astrochimiques (PIRENEA) and imaging photoelectron photoion coincidence spectrometry (iPEPICO). In total, 22 reactions, involving the fragmentation cascade (H, C2H2, and C4H2 loss) from the pyrene radical cation down to the C14(+•) fragment ion, have been studied using PIRENEA. Branching ratios have been measured for reactions from C16H10(+•), C16H8(+•), and C16H5(+). Density functional theory calculations of the fragmentation pathways observed experimentally and postulated theoretically lead to 17 unique structures. One important prediction is the opening of the pyrene ring system starting from the C16H4(+•) radical. In the iPEPICO experiments, only two reactions could be studied, namely, R1 C16H10(+•) → C16H9(+) + H (m/z = 201) and R2 C16H9(+) → C16H8(+•) + H (m/z = 200). The activation energies for these reactions were determined to be 5.4 ± 1.2 and 3.3 ± 1.1 eV, respectively.

Assessment of insulin action in insulin-dependent diabetes mellitus using [6(14)C]glucose, [3(3)H]glucose, and [2(3)H]glucose. Differences in the apparent pattern of insulin resistance depending on the isotope used

International Nuclear Information System (INIS)

Bell, P.M.; Firth, R.G.; Rizza, R.A.

1986-01-01

To determine whether [2(3)H], [3(3)H], and [6(14)C]glucose provide an equivalent assessment of glucose turnover in insulin-dependent diabetes mellitus (IDDM) and nondiabetic man, glucose utilization rates were measured using a simultaneous infusion of these isotopes before and during hyperinsulinemic euglycemic clamps. In the nondiabetic subjects, glucose turnover rates determined with [6(14)C]glucose during insulin infusion were lower (P less than 0.02) than those determined with [2(3)H]glucose and higher (P less than 0.01) than those determined with [3(3)H]glucose. In IDDM, glucose turnover rates measured with [6(14)C]glucose during insulin infusion were lower (P less than 0.05) than those determined with [2(3)H]glucose, but were not different from those determined with [3(3)H]glucose. All three isotopes indicated the presence of insulin resistance. However, using [3(3)H]glucose led to the erroneous conclusion that glucose utilization was not significantly decreased at high insulin concentrations in the diabetic patients. [6(14)C] and [3(3)H]glucose but not [2(3)H]glucose indicated impairment in insulin-induced suppression of glucose production. These results indicate that tritiated isotopes do not necessarily equally reflect the pattern of glucose metabolism in diabetic and nondiabetic man

Correlation factors for C-14, Cl-36, Ni-59, Ni-63, Mo-93, Tc-99, I-129 and Cs-135. In operational waste for SFR 1

Energy Technology Data Exchange (ETDEWEB)

Lindgren, Maria; Pettersson, Michael; Wiborgh, Marie (Kemakta AB, Stockholm (SE))

2007-01-15

The use of correlation factors is one possibility to estimate a reference radionuclide inventory for the purpose of safety assessment studies, when waste-type specific information is not at hand. The correlation factor approach requires that there is a correlation between the activity content of the difficult-to-measure nuclide and the key nuclide. A safety assessment of a future deep repository for low and intermediate level waste (SFL 3-5) was conducted during the second half of the 1990's. Within that project, correlation factors for estimating the inventory of radionuclides which are difficult to measure experimentally were developed. These factors have also partly been used to estimate a reference inventory for SFR 1. Based on a literature survey and recent reports published by SKB, it is concluded that new information is available making an update of some correlation factors relevant. For these radionuclides, reported data from estimations and measurements of radionuclide content and correlation factors in different types of radioactive wastes are summarised. The data is evaluated and updated correlation factors representative for fresh waste for eight radionuclides (C-14, Cl-36, Ni-59, Ni-63, Mo-93, Tc-99, I-129 and Cs-135) are suggested. New information from measurements in Swedish NPP has made it possible to define factors that are BWR and PWR specific for C-14, Ni-59 and Ni-63. The uncertainties in suggested data and the applicability of the correlation factors for estimates of the radionuclide content in operational waste are commented upon

Relative turnover of [3H]arachidonic acid and [14C]eicosapentaenoic acid in stimulated human platelets

International Nuclear Information System (INIS)

Weaver, B.J.; Holub, B.J.

1986-01-01

The relative release of arachidonic acid (AA) versus eicosapentaenoic acid (EPA) from platelet phospholipids may be important in accounting for the potential of dietary fish oil containing EPA to alter platelet reactivity. Human platelets enriched in EPA and prelabelled with [ 3 H]AA and [ 14 C]EPA were used to examine the relative losses of these fatty acids from platelet phospholipids upon stimulation. Washed dual-labelled platelets were incubated with and without thrombin in the presence of BW755C and in the presence and absence of trifluoperazine. The platelet lipids were extracted and the individual phospholipids as well as diacylglycerol (DG), phosphatidic acid (PA), etc. were separated by thin-layer chromatography and the radioactivity in each fraction determined. The [ 3 H]AA/[ 14 C]EPA dpm ratio for the loss in radioactivity from PC upon thrombin stimulation was similar to that for the PC in resting platelets. This suggests no marked selectivity in the degradation of AA versus EPA species of PC during platelet activation. The [ 3 H]/[ 14 C] ratios for the increased radioactivity in DG and PA upon thrombin stimulation were slightly higher than the ratio in PI from resting platelets suggesting only a minor preference for 1-acyl 2-arachidonoyl PI over 1-acyl 2-eicosapentaenoyl PI in the pathway from PI to DG to PA

catena-Poly[[[aquasilver(I]-μ-1,1′-(butane-1,4-diyldi-1H-imidazole-κ2N3:N3′] hemi(biphenyl-4,4′-dicarboxylate dihydrate

Directory of Open Access Journals (Sweden)

Zheyu Zhang

2009-12-01

Full Text Available In the title compound, {[Ag(C10H14N4(H2O](C14H8O40.5·2H2O}n, the AgI ion is three-coordinated by two N atoms from two independent 1,1′-(butane-1,4-diyldi-1H-imidazole (BBI ligands and one water O atom in a distorted T-shaped coordination geometry. The biphenyl-4,4′-dicarboxylate (BPDC dianions do not coordinate to AgI ions but act as counter-ions. The AgI ions are linked by BBI ligands, forming a zigzag chain. These chains are linked into a two-dimensional supramolecular architecture by O—H...O hydrogen-bonding interactions between water molecules and carboxylate O atoms of the BPDC dianions.

Speciation of 127I and 129I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

Directory of Open Access Journals (Sweden)

L. Zhang

2016-02-01

Full Text Available Speciation analysis of iodine in aerosols is a very useful approach for understanding geochemical cycling of iodine in the atmosphere. In this study, overall iodine species, including water-soluble iodine species (iodide, iodate and water-soluble organic iodine, NaOH-soluble iodine, and insoluble iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, during March and May 2011 (shortly after the Fukushima nuclear accident and in December 2014. The measured concentrations of total iodine are in the range of 1.04–2.48 ng m−3 for 127I and (11.3–97.0  ×  105 atoms m−3 for 129I, corresponding to 129I ∕ 127I atomic ratios of (17.8–86.8  ×  10−8. The contribution of Fukushima-derived 129I (peak value of 6.3  ×  104 atoms m−3 is estimated to be negligible (less than 6 % compared to the total 129I concentration in northern Europe. The concentrations and species of 129I and 127I in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated seas contained higher concentrations of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed to secondary emission of marine discharged 129I in the contaminated seawater in the North Sea, North Atlantic Ocean, English Channel, Kattegat, etc., rather than direct gaseous release from the European nuclear reprocessing plants (NRPs. Water-soluble iodine was found to be a minor fraction to the total iodine for both 127I (7.8–13.7 % and 129I (6.5–14.1 % in ocean-derived aerosols, but accounted for 20.2–30.3 % for 127I and 25.6–29.5 % for 129I in land-derived aerosols. Iodide was the predominant form of water-soluble iodine, accounting for more than 97 % of the water-soluble iodine. NaOH-soluble iodine seems to be independent of the sources of aerosols. The significant

Optimisation of the measurement protocols of {sup 129}I and {sup 129}I/{sup 127}I. Methodology establishment for the measurement in environmental matrices; Optimisation des protocoles de mesurage de {sup 129}I et {sup 129}I/{sup 127}I. Etablissement d'une methodologie adaptee aux echantillons de l'environnement

Energy Technology Data Exchange (ETDEWEB)

Frechou, C

2000-07-01

{sup 129}I, is a natural long-lived isotope, with a half-life of 15,7 million years, also artificially produced in nuclear power plant. It is then released in the liquid and gaseous effluents of the nuclear fuel reprocessing plants. {sup 129}I is integrated in all biological compartments at different activity levels, depending on their distance from the emission source and their ability to metabolize iodine. Performances of the different {sup 129}I and {sup 129}I/{sup 127}I measurement techniques available: Radiochemical Neutron Activation Analysis, Accelerator Mass Spectrometry, direct {gamma}-X spectrometry and liquid scintillation were evaluated. Associated radiochemical preparation steps of the two first techniques were optimized and adapted to the characteristics of the major environmental matrices. In a first step, the radiochemical protocols were developed and validated. In a second step, intercomparison exercises have been lead on various environmental samples presenting different {sup 129}I activity levels. They showed the good agreement between the results given by the three techniques on different environmental matrices with activities between 0,2 and 200 Bq.kg{sup -1} dry weight. As a conclusion, a methodology for the measurement of {sup 129}I and {sup 129}I/{sup 127}I ratio in environmental samples is proposed. It includes a decisional diagram taking into account the characteristics of the matrices, the detection limits and the answer delay. A study on the losses of {sup 129}I during the calcination of an algae was lead by direct {gamma}-X spectrometry and application studies were made to measure {sup 129}I levels in different biological compartments issued from various locations: {sup 129}I activity interspecific variation in different species of seaweeds from the French channel coast under the relative influence of La Hague, {sup 129}I levels in bovine thyroids from the Cotentin area and {sup 129}I in vegetal samples collected around the nuclear

Synthesis of [3-14C]- and [phenyl-U-14C] olaquindox

International Nuclear Information System (INIS)

Maul, W.; Scherling, D.; Seng, F.

1981-01-01

Olaquindox is a new feed additive. [ 14 C]Olaquindox, labelled in different positions, was needed for tracer-studies of pharmacokinetics, biotransformation and residues in several species of animals. 2-[N-(2-hydroxethyl)-carbamoyl]-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide([3- 14 C]Olaquindox) was synthesized from barium[ 14 C]carbonate (22 mmoles; 1.15 Ci) via [1- 14 C]acetic acid, sodium[1- 14 C]acetate, [1- 14 C]acetylchloride, ethyl[3- 14 C]acetoacetate and 2-carbethoxy-3-methyl-[3- 14 C]quinoxaline-1,4-dioxide with an overall yield of 10%, based on barium[ 14 C]carbonate. The radiochemical purity was better than 98% (tlc). The specific activities of three preparations were 10.5, 8.4 and 5.45 μCi/mg respectively. [phenyl-U- 14 C]Olaquindox was synthesized starting from [U- 14 C]aniline (19.8 mmoles; 284.4 mCi). Intermediate products were N-acetyl[U- 14 C]aniline, 2-nitro-N-acetyl[U- 14 C]aniline, 2-nitro[U- 14 C]aniline and [U- 14 C]benzofurazanoxide. The total yield was 50% as calculated for [U- 14 C]aniline. At calibration samples of two preparations showed specific activities of 49.5 and 11.1 μCi/mg respectively. The radiochemical purity was checked by tlc and exceeded 98%. (author)

Some biological consequences of disintegration of 3H and 14C incorporated in an influenza virus

International Nuclear Information System (INIS)

Prokudina, E.N.; Semenova, N.P.; Yamnikova, S.S.; Zhdanov, V.M.

1987-01-01

An influenza virus labeled with 3 H-uridine losses its infectiousness when stored for a long time. It is suggested that disintegration of tritium incorporated into virus RNA causes lethal intramolecular modifications therein. At the same time, the antigenic activity of virus nucleoprotein decreases perhaps due to the direct effect of tritium. The comparison of the degree of inactivation of various antigenic sites of the nucleoprotein within a virus, labeled with 3 H-uridine, suggests that they are located at different distances from RNA. A long-term action of 3 H disintegration on RNA of a maturing virus decreased the yield probably due to the injury of the intracellular virus RNA during the infections process. Upon storage of the influenza virus labelle with 14 C-amino acids the antigenic properties are reduced by the nucleoprotein while the infectiousness remains unaffected. The long-term effect of 14 C disintegration on proteins of the maturing virus does not lead to fatal outcome

A two emulsion autoradiographic technique and the discriminating of the three different types of labelling after double labelling with 3H- and 14C-thymidine

International Nuclear Information System (INIS)

Schultze, B.; Maurer, W.; Hagenbusch, H.

1976-01-01

The first part of the paper deals with a two emulsion autoradiographic technique for double labelling experiments with 3 H- and 14 C-thymidine which permits a clear discrimination of the different types of labelling. In the second part the application of this technique to cell kinetics studies is discussed. Accurate discrimination between the different types of labelling, namely purely 3 H-, purely 14 C- and double ( 3 H + 14 C) labelling, is only possible if the activity ratio of 3 H- to 14 C-thymidine is sufficiently high. This condition is necessary for a reliable distinction between those grains in the first emulsion which are due to true 3 H-labelling and spurious grains which are simultaneously produced in the same emulsion by 14 C-β- particles. Experiments are described to determine the required activity ratio of 3 H- to 14 C-thymidine. (author)

Electro-removal of H-3 and C-14 contained in scintillation liquid absorbed in soils type Phaeozem

International Nuclear Information System (INIS)

Valdovinos, V.; Bustos, E.; Monroy G, F.

2014-10-01

This paper presents the results of electro-removal, an electrochemical treatment in soils contaminated with H-3 and C-14 contained in scintillation liquids absorbed in soils. For this purpose the best electrochemical conditions were used, which are: scintillation liquid Ultima Gold Xr, water (1:1) and 1 m A in the passage of current. The media were characterized before and after of applying the different potentials by various analytical techniques, such as: liquids by gas chromatography with a flame ionization detector, solids and liquids by Fourier transform infrared spectroscopy (Ftir) and electrodes by scanning electron microscopy with elemental analysis by energy-dispersive X-ray spectroscopy. Later standard samples with H-3 and C-14 were prepared and the electrochemical treatment was applied to previously established conditions. After electrochemical treatment the scintillation liquid characterization was performed by gas chromatography and a scintillation counter to see the disintegrations per minute. According to results of Ftir, soils show no deterioration and in the liquid phase the amount of water increases as the applied potential, due to oxidation-reduction reactions where happen modification or mineralization of organic molecules (H 2 O and CO 2 formation). In 4 h of treatment, removal percentages in the liquid phase, were: 53.6% of H-3 and 11.6% of C-14. (Author)

Synthesis and crystal structure of new uranyl selenite(IV)-selenate(VI) [C5H14N][(UO2)3(SeO4)4(HSeO3)(H2O)](H2SeO3)(HSeO4)

International Nuclear Information System (INIS)

Krivovichev, S.V.; Tananaev, I.G.; Myasoedov, B.F.; Kalenberg, V.

2006-01-01

Crystals of new uranyl selenite(IV)-selenate(VI) [C 5 H 14 N][(UO 2 ) 3 (SeO 4 ) 4 (HSeO 3 )(H 2 O)](H 2 SeO 3 )(HSeO 4 ) are obtained by the method of evaporation from aqueous solutions. Compound has triclinic lattice, space group P1-bar, a=11.7068(9), b=14.8165(12), c=16.9766(15), α=73.899(6), β=76.221(7), γ=89.361(6) Deg, V=2743.0(4) A 3 , Z=2. Laminated complexes (UO 2 ) 3 (SeO 4 ) 4 (HSeO 3 )(H 2 O)] 3- are the basis of the structure. [HSe(VI)O 4 ] - , [H 2 Se(IV)O 3 ] complexes and protonated methylbutylamine cations are disposed between layers [ru

Speciation of {sup 127}I and {sup 129}I in atmospheric aerosols at Risoe, Denmark. Insight into sources of iodine isotopes and their species transformations

Energy Technology Data Exchange (ETDEWEB)

Zhang, Luyuan; Hou, Xiaolin [Technical Univ. of Denmark, Roskilde (Denmark). Center for Nuclear Technologies; Chinese Academy of Sciences, Xi' an (China). State Key Laboratory of Loess and Quaternary Geology; Xu, Sheng [Scottish Universities Environmental Research Center, East Kilbride (United Kingdom)

2016-07-01

Speciation analysis of iodine in aerosols is a very useful approach for understanding geochemical cycling of iodine in the atmosphere. In this study, overall iodine species, including water-soluble iodine species (iodide, iodate and water-soluble organic iodine), NaOH-soluble iodine, and insoluble iodine have been determined for {sup 129}I and {sup 127}I in the aerosols collected at Risoe, Denmark, during March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04-2.48 ngm{sup -3} for {sup 127}I and (11.3-97.0) x 10{sup 5} atoms m{sup -3} for {sup 129}I, corresponding to {sup 129}I/{sup 127}I atomic ratios of (17.8-86.8) x 10{sup -8}. The contribution of Fukushima-derived {sup 129}I (peak value of 6.3 x 10{sup 4} atoms m{sup -3}) is estimated to be negligible (less than 6 %) compared to the total {sup 129}I concentration in northern Europe. The concentrations and species of {sup 129}I and {sup 127}I in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated seas contained higher concentrations of {sup 129}I than aerosols transported over the European continent. The high {sup 129}I concentrations of the marine aerosols are attributed to secondary emission of marine discharged {sup 129}I in the contaminated seawater in the North Sea, North Atlantic Ocean, English Channel, Kattegat, etc., rather than direct gaseous release from the European nuclear reprocessing plants (NRPs). Water-soluble iodine was found to be a minor fraction to the total iodine for both {sup 127}I (7.8-13.7 %) and {sup 129}I (6.5-14.1 %) in ocean-derived aerosols, but accounted for 20.2-30.3% for {sup 127}I and 25.6-29.5 % for {sup 129}I in land-derived aerosols. Iodide was the predominant form of water-soluble iodine, accounting for more than 97 % of the water-soluble iodine. NaOH-soluble iodine seems to be

Synthesis of /sup 14/C- and /sup 3/H-labelled 4-(4-nitrophenyl)aminophenylisothiocyanate (Go 9333/CGP 4540; amoscanate)

Energy Technology Data Exchange (ETDEWEB)

Anjaneyulu, B.; Maller, R.K.; Nagarajan, K. (Hindustan Ciba-Geigy Ltd., Bombay (India). Isotope Lab.); Kueng, W.; Wirz, B. (Ciba-Geigy A.G., Basel (Switzerland))

1985-04-01

Amoscanate, a broad spectrum anthelmintic, labelled with carbon-14 on the isothiocyanate carbon atom was prepared in an overall yield of 13% at a specific activity of 4.13 ..mu..Ci/mg from potassium (/sup 14/C)thiocyanate. The 4-nitro(U-/sup 14/C)phenyl ring labelled compound was synthesized in 20.4% overall yield from (U-/sup 14/C)aniline at a specific activity of 12.2 ..mu..Ci/mg. The corresponding tritiated compound was prepared from 4-amino(2-/sup 3/H)acetanilide at 112 ..mu..Ci/mg. Labelling with tritium in the aromatic ring bearing the isothiocyanate group was achieved by catalysed halogen-tritium replacement. However, for pharmacokinetic and metabolism studies in experimental animals, the /sup 14/C- and /sup 3/H-labels associated with the phenylisothiocyanate moiety subsequently proved disadvantageous because of the instability of the labels in vivo.

Bis[μ-3-(1H-benzimidazol-2-ylbenzoato]dicopper(I

Directory of Open Access Journals (Sweden)

Zheng-Yu Su

2010-12-01

Full Text Available The dimeric title complex, [Cu2(C14H9N2O22], resides on a center of symmetry. In the crystal, the molecules are packed via π–π stacking interactions alternating between imidazole and benzene rings [mean interplanar distances = 3.754 (3 and 3.624 (3 Å]. An intermolecular N—H...O hydrogen bond links the dimers together. The two-coordinate CuI atom displays an O—Cu—N bond angle of 176.3 (2°. The Cu...Cu distance within the dimer is 5.100 (2 Å.

TMEM129 is a Derlin-1 associated ERAD E3 ligase essential for virus-induced degradation of MHC-I.

Science.gov (United States)

van den Boomen, Dick J H; Timms, Richard T; Grice, Guinevere L; Stagg, Helen R; Skødt, Karsten; Dougan, Gordon; Nathan, James A; Lehner, Paul J

2014-08-05

The US11 gene product of human cytomegalovirus promotes viral immune evasion by hijacking the endoplasmic reticulum (ER)-associated degradation (ERAD) pathway. US11 initiates dislocation of newly translocated MHC I from the ER to the cytosol for proteasome-mediated degradation. Despite the critical role for ubiquitin in this degradation pathway, the responsible E3 ligase is unknown. In a forward genetic screen for host ERAD components hijacked by US11 in near-haploid KBM7 cells, we identified TMEM129, an uncharacterized polytopic membrane protein. TMEM129 is essential and rate-limiting for US11-mediated MHC-I degradation and acts as a novel ER resident E3 ubiquitin ligase. TMEM129 contains an unusual cysteine-only RING with intrinsic E3 ligase activity and is recruited to US11 via Derlin-1. Together with its E2 conjugase Ube2J2, TMEM129 is responsible for the ubiquitination, dislocation, and subsequent degradation of US11-associated MHC-I. US11 engages two degradation pathways: a Derlin-1/TMEM129-dependent pathway required for MHC-I degradation and a SEL1L/HRD1-dependent pathway required for "free" US11 degradation. Our data show that TMEM129 is a novel ERAD E3 ligase and the central component of a novel mammalian ERAD complex.

Monitoring intervals for measurement of the radionuclides 125 I and 129I in thyroid glands

International Nuclear Information System (INIS)

Simanca, Yoan Yera; Bejerano, Gladys M. Lopez

2013-01-01

This work shows the monitoring interval, which can be implemented in the Laboratorio de Contaminacion Interna del Centro de Proteccion e Higiene de las Radiaciones, for direct measurement in the thyroid gland of radionuclides 125 I and 129 I . Were used two measuring systems, one employing a scintillating detector and the other detector Phoswich. Both detectors were placed inside a depth camera, 2.5 x 2.5 x 2.5m of dimension covered with 15 cm of steel, 3 mm lead, 1.8 mm tin and 1.5 mm of copper. Was calculated for each system, the minimum detectable activity, and based on this, the monitoring interval is determined. Was obtained, for 125 , all tested intervals, 120, 90,60,30 , 14, and 7 days may be implemented with both systems. In the case of the radionuclide 129 I, with the installation of scintillating detector can only be implemented the intervals 120, 90, and 60 days , and for installation with Phoswich, all evaluated

Determination method for 129I in soil samples by MIP-MS

International Nuclear Information System (INIS)

Uezu, Yasuhiro; Nakano, Masanao; Fujita, Hiroki; Watanabe, Hitoshi; Maruo, Yoshihiro

2001-01-01

The radioactive iodine-129 ( 129 I) is an important radionuclide for environmental assessment because it has a long half-life and is accumulated in the thyroid gland in humans. A new analytical technique by Microwave Induced Plasma Mass Spectrometer (MIP-MS) was applied to the determination of 129 I in soil samples. In environmental samples, a large amount of matrix elements are present. Therefore, the matrix elements were eliminated by ashing at 1000degC, and iodine isotopes were trapped by an activated charcoal and finally extracted by 10% tetramethylammonium hydroxide (TMAH). The concentration of 129 I in a soil samples were compared between results of neutron activation analysis and MIP-MS method. The results showed an excellent agreement. (author)

Conversion of pregnenolone 16-3H and progesterone-4-14C to radioactive testosterone by the 18-day embryonic mouse testis

International Nuclear Information System (INIS)

Pointis, Georges; Lombard, M.-N.; Guichard, Arlette; Cedard, Lise

1975-01-01

Fetal mice testes convert pregnenolone-16- 3 H and progesterone-4- 14 C to testosterone in organ culture. The 3 H/ 14 C ratio in progesterone and testosterone fractions isolated from culture media suggests the importance of the Δ 5- 3β hydroxysteroid pathway in the experimental conditions. LH decreases radioactive testosterone production and increases the activity of the Δ 4 -3-ketosteroid pathway [fr

Speciation and migration of 129I in soil profiles

International Nuclear Information System (INIS)

Luo, Maoyi; Hou, Xiaolin; Zhou, Weijian; He, Chaohui; Chen, Ning; Liu, Qi; Zhang, Luoyuan

2013-01-01

A method has been developed for speciation analysis of ultra low level 129 I in soil using sequential extraction combined with coprecipitation for separation of carrier free iodine and AMS measurement of 129 I. Two loess profiles collected from northwest China were analyzed for species of 129 I and 127 I. Similar partitioning of 129 I and 127 I was observed in the loess profiles, the distribution of iodine isotopes followed an order of organic > leachable > reducible > residue. The 129 I concentrations and 129 I/ 127 I ratios decreased exponentially with the depth, and 2 orders of magnitude lower in the deepest layer (60 and 90 cm) compared with the top layer, indicating a significant contribution of anthropogenic input in the upper layer, and high retention of 129 I in soil. The mobility of 129 I in different fractions decreased in an order of leachable > organic > oxides > residue. The results suggest that migration of iodine downwards in the soil profile is a slow process; the oxides and residue are the less mobile fractions of iodine. Highlights: ► 129 I concentration decreases exponentially with the depth of soil profile. ► The mobility of 129 I in fractions decreases: leachable > organic > oxides > residue. ► Iodine shows less mobility in oxides and residue fractions. ► High organic soil content can effectively reduce the migration of 129 I in the environment. ► Carrier free iodine AMS is an effective method for natural 129 I speciation analysis in the environment

Crystallographic characterization of divalent organosamarium compound (C5H5)2Sm(THF)2

International Nuclear Information System (INIS)

Jagannatha Swamy, S.

2002-01-01

The single pot reaction between SmX 2 (X = Cl - , I - ) and BuLi in THF at -40 degC, followed by the addition of C 5 H 5 - Na + results in a dark red solution. Leaving the concentrated reaction mixture at -25 degC for two days in a deep freezer results in the formation of the crystals of the compound, (C 5 H 5 ) 2 ; Sm(THF) 2 . The compound is insoluble in any solvent and it has been characterized by conventional methods. The crystals are monoclinic with space group C2/c, and a = 13.416(1), b = 9.644(1), c = 14.129(2) pm, β109.873(9) 0 and z = 4 for ρcalcd = 1.64 g cm -3 . Least squares refinement on the basis of 1804 observed reflections has led to a final R value of 0.037 and R w = 0.054. (author)

Investigation of ZnI2-KI-C3H7NO system by ultrasonic method

International Nuclear Information System (INIS)

Shevchenko, V.M.; Surovtsev, V.I.; Gorenbejn, E.Ya.

1975-01-01

Applicability of the ultrasonic impulses for the research of complex formation in the solutions was demonstrated using ZnI 2 -KI-C 3 H 7 NO system as an example. Changing the solvent structure during complexing was studied. It was determined that ion solvation numbers reflect electrostriction influence of ions on the surrounding solvent moleculas. The maximum effect on dimethylformamide (C 3 H 7 NO) was made by the complex compound KZnI 3 acting as destrictor and the sound speed decrease was the highest in its solution. Possibility of using adiabatic compressibility of the solutions for complexing studies is analysed

Silver-based getters for 129I removal from low-activity waste

International Nuclear Information System (INIS)

Asmussen, R. Matthew; Neeway, James J.; Lawter, Amanda R.; Wilson, Andrew; Qafoku, Nikolla P.

2016-01-01

A prominent radionuclide of concern in nuclear wastes, 129 I, is present in low-activity wastes (LAW) at the Hanford site. Several Ag-containing materials were tested as immobilization agents, or ''getters'', for I (as iodide, I - ) removal from deionized (DI) water and a liquid LAW simulant: Ag impregnated activate carbon (Ag-C), Ag exchanged zeolite (Ag-Z), and argentite. In anoxic batch experiments with DI water, the Ag-C and argentite were most effective, with maximum K d values of 6.2 x 10 5 mL/g for the Ag-C and 3.7 x 10 5 mL/g for the argentite after 15 days. Surface area and Ag content were found to influence the performance of the getters in DI water. In the anoxic batch experiments with LAW simulant, Ag-Z vastly outperformed the other getters with K d values of 2.2 x 10 4 mL/g at 2 h, which held steady until 15 days, compared with 1.8 x 10 3 mL/g reached at 15 days by the argentite. All getters were stable over long periods of time (i.e. 40 days) in DI water, while the Ag-Z and argentite were also stable in the LAW simulant. Ag-Z was found to have consistent I removal upon crushing to a smaller particle size and in the presence of O 2 , making it a strong candidate for the treatment of LAW containing I.

Underestimation of glucose turnover measured with [6-3H]- and [6,6-2H]- but not [6-14C]glucose during hyperinsulinemia in humans

International Nuclear Information System (INIS)

McMahon, M.M.; Schwenk, W.F.; Haymond, M.W.; Rizza, R.A.

1989-01-01

Recent studies indicate that hydrogen-labeled glucose tracers underestimate glucose turnover in humans under conditions of high flux. The cause of this underestimation is unknown. To determine whether the error is time-, pool-, model-, or insulin-dependent, glucose turnover was measured simultaneously with [6-3H]-, [6,6-2H2]-, and [6-14C]glucose during a 7-h infusion of either insulin (1 mU.kg-1.min-1) or saline. During the insulin infusion, steady-state glucose turnover measured with both [6-3H]glucose (8.0 +/- 0.5 mg.kg-1.min-1) and [6,6-2H2]glucose (7.6 +/- 0.5 mg.kg-1.min-1) was lower (P less than .01) than either the glucose infusion rate required to maintain euglycemia (9.8 +/- 0.7 mg.kg-1.min-1) or glucose turnover determined with [6-14C]glucose and corrected for Cori cycle activity (9.8 +/- 0.7 mg.kg-1.min-1). Consequently negative glucose production rates (P less than .01) were obtained with either [6-3H]- or [6,6-2H2]- but not [6-14C]glucose. The difference between turnover estimated with [6-3H]glucose and actual glucose disposal (or 14C glucose flux) did not decrease with time and was not dependent on duration of isotope infusion. During saline infusion, estimates of glucose turnover were similar regardless of the glucose tracer used. High-performance liquid chromatography of the radioactive glucose tracer and plasma revealed the presence of a tritiated nonglucose contaminant. Although the contaminant represented only 1.5% of the radioactivity in the [6-3H]glucose infusate, its clearance was 10-fold less (P less than .001) than that of [6-3H]glucose. This resulted in accumulation in plasma, with the contaminant accounting for 16.6 +/- 2.09 and 10.8 +/- 0.9% of what customarily is assumed to be plasma glucose radioactivity during the insulin or saline infusion, respectively (P less than .01)

Catalyst-Dependent Chemoselective Formal Insertion of Diazo Compounds into C-C or C-H Bonds of 1,3-Dicarbonyl Compounds.

Science.gov (United States)

Liu, Zhaohong; Sivaguru, Paramasivam; Zanoni, Giuseppe; Anderson, Edward A; Bi, Xihe

2018-05-08

A catalyst-dependent chemoselective one-carbon insertion of diazo compounds into the C-C or C-H bonds of 1,3-dicarbonyl species is reported. In the presence of silver(I) triflate, diazo insertion into the C(=O)-C bond of the 1,3-dicarbonyl substrate leads to a 1,4-dicarbonyl product containing an all-carbon α-quaternary center. This reaction constitutes the first example of an insertion of diazo-derived carbenoids into acyclic C-C bonds. When instead scandium(III) triflate was applied as the catalyst, the reaction pathway switched to formal C-H insertion, affording 2-alkylated 1,3-dicarbonyl products. Different reaction pathways are proposed to account for this powerful catalyst-dependent chemoselectivity. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Field-induced spin splitting and anomalous photoluminescence circular polarization in C H3N H3Pb I3 films at high magnetic field

Science.gov (United States)

Zhang, Chuang; Sun, Dali; Yu, Zhi-Gang; Sheng, Chuan-Xiang; McGill, Stephen; Semenov, Dmitry; Vardeny, Zeev Valy

2018-04-01

The organic-inorganic hybrid perovskites show excellent optical and electrical properties for photovoltaic and a myriad of other optoelectronics applications. Using high-field magneto-optical measurements up to 17.5 T at cryogenic temperatures, we have studied the spin-dependent optical transitions in the prototype C H3N H3Pb I3 , which are manifested in the field-induced circularly polarized photoluminescence emission. The energy splitting between left and right circularly polarized emission bands is measured to be ˜1.5 meV at 17.5 T, from which we obtained an exciton effective g factor of ˜1.32. Also from the photoluminescence diamagnetic shift we estimate the exciton binding energy to be ˜17 meV at low temperature. Surprisingly, the corresponding field-induced circular polarization is "anomalous" in that the photoluminescence emission of the higher split energy band is stronger than that of the lower split band. This "reversed" intensity ratio originates from the combination of long electron spin relaxation time and hole negative g factor in C H3N H3Pb I3 , which are in agreement with a model based on the k.p effective-mass approximation.

Studies on 129I in bovine thyroid glands and investigations on revolatilization of iodine

International Nuclear Information System (INIS)

Glubrecht, H.; Kiselnic, L.; Handl, J.; Kuehn, W.

1979-01-01

In order to study fall out effect, deposition and revolatilization of iodine in the field and 129 I activity in bovine thyroid glands were studied. Deposition velocity of I 2 was 0.15 to 7 cm/sec, which was 100 times higher than that of CH 3 I. Biological half-life of iodine was 7.5 +- 0.5 d. In the contaminated plants, indifferent to the environmental conditions. However, the decrease of iodine concentration was not observed when the plants were cut off immediately after deposition of iodine. A sample of soil with or without plants was contaminated with iodine and re-emitted iodine was trapped by a charcoal filter. Iodine concentration was determined by I-specific electrodes after 1, 2, 4, and 8 hrs. In any case, I 2 was re-emitted immediately after the contamination. Bovine thyroid glands were dried by deep freezing and ground after the addition of KOH. Organic compounds were decomposed by stepwise heating up to 600 0 C. Then iodine was extracted by concentrated H 2 SO 4 and heated at 110 0 C. Evaporating iodine was adsorbed by a pure charcoal filter. By neutron activation analysis of the filter the activity of 129 I was 1.2 pCi/g iodine, which would be about 5 times higher than that measured in animals living far from nuclear installations. The distribution of stable iodine in thyroid gland was inhomogeneous. (Nakanishi, T.)

Synthesis of 11-14C-quetiapine, 11-14C-isoclotiapine and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10-14C

International Nuclear Information System (INIS)

Naghi Saadatjoo; Mohsen Javaheri; Nuclear Science and Technology Research Institute, Tehran; Nader Saemian; Mohsen Amini

2016-01-01

Quetiapine is one of the most widely used antipsychotic drug which acts as an antagonist for multiple neurotransmitter receptor sites. 2-[2-(4-(Dibenzo[b,f][1,4]thiazepin-11-yl)piperazin-1-yl)ethoxy]ethanol (quetiapine) labeled with carbon-14 in 11-position has been synthesized as part of a 5-step sequence from anthranilic acid-[carboxy- 14 C]. We have presented a convenient synthetic pathway for labeling of quetiapine with carbon-14 by using one-pot procedures from a key thiazepin-11(10H)-one-[11- 14 C] by good radiochemical yield. And also isoclotiapine[11- 14 C], and 10-(4-methylpiperazin-1-yl)pyrido[4,3-b][1,4]benzothiazepine[10- 14 C], synthesized according to this route. (author)

Speciation of ¹²⁷I and ¹²⁹I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin; Xu, Sheng

2016-01-01

iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, between March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04–2.48 ng m−3 for 127I and (11.3–97.0) × 105 atoms m...... in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated ocean, contained higher amounts of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed...... to secondary emission from heavily 129I-contaminated seawater rather than primary gaseous release from nuclear reprocessing plants. Water-soluble iodine was found to be a minor fraction to total iodine for both 127I (7.8–13.7 %) and 129I (6.5–14.1 %) in ocean-derived aerosols, but accounted for 20...

Speciation of ¹²⁷I and ¹²⁹I in atmospheric aerosols at Risø, Denmark: insight into sources of iodine isotopes and their species transformations

DEFF Research Database (Denmark)

Zhang, Luyuan; Hou, Xiaolin; Xu, Sheng

2015-01-01

iodine have been determined for 129I and 127I in the aerosols collected at Risø, Denmark, between March and May 2011 (shortly after the Fukushima nuclear accident) and in December 2014. The measured concentrations of total iodine are in the range of 1.04–2.48 ng m−3 for 127I and (11.3–97.0) × 105 atoms m...... in the aerosols are found to be strongly related to their sources and atmospheric pathways. Aerosols that were transported over the contaminated ocean, contained higher amounts of 129I than aerosols transported over the European continent. The high 129I concentrations of the marine aerosols are attributed...... to secondary emission from heavily 129I-contaminated seawater rather than primary gaseous release from nuclear reprocessing plants. Water-soluble iodine was found to be a minor fraction to total iodine for both 127I (7.8–13.7 %) and 129I (6.5–14.1 %) in ocean-derived aerosols, but accounted for 20...

Synthesis of [3,5-14C]trachelanthamidine and [5-3H]isoretronecanol and their incorporation into the retronecine moiety of riddelliine in Senecio riddellii

International Nuclear Information System (INIS)

Leete, E.; Rana, J.

1986-01-01

(+/-)-[3,5- 14 C]Trachelanthamidine and (+/-)-[5- 3 H]isoretronecanol, which are diastereomers, were prepared from potassium [ 14 C]cyanide and [5- 3 H]proline, respectively. These compounds and [1,4- 14 C]putrescine were administered to Senecio riddellii plants resulting in the formation of labeled riddelliine, in which almost all the radioactivity was located in its retronecine moiety. The activity of the beta-alanine obtained by degradation of the retronecine was consistent with specific labeling of this pyrrolizidine base at the expected positions. The extremely high absolute incorporation (15.1, 22.1%) of trachelanthamidine into riddelliine strongly favors this 1-hydroxymethylpyrrolizidine as the one on the main biosynthetic pathway to retronecine. The lower incorporation (0.75%) of isoretronecanol may represent a minor or aberrant pathway to retronecine

Ceramic phases for immobilization of 129I

International Nuclear Information System (INIS)

Vance, E.R.; Agrawal, D.K.; Scheetz, B.E.; Pepin, J.G.; Atkinson, S.D.; White, W.B.

1981-01-01

Materials for ultimate disposal of 129 I have been studied. At present, iodide-sodalite, though not ideal, appears to be the best material for 129 I immobilization from the aspects of ease of preparation, thermal stability, cost of materials, and leach resistance. Good consolidation of the material was achieved by sintering in air at 1000 to 1200 0 C, but the iodine content was significantly below stoichiometric expectations. Hot aqueous media preferentially removed iodine, apparently by OH - substitution in near-neutral solutions, and I reversible reaction Cl - exchange occurred in brine. Alternation of the sodalite also took place. Soxhlet leach rates were about 5 x 10 -4 g/cm 2 -day by total weight loss, but physical weathering contributed significantly to this value. Moderate doses of radiation had no observable deleterious structural effects. Iodoboracites seemingly cannot be prepared by ceramic or nonhydrothermal wet chemical techniques. Fe-iodoboracite has inferior thermal stability to iodide-sodalite and was completely altered to hematite after treatment at 200 0 C in deionized water. Silver zeolites retained some iodine in the form of crystalline α-AgI at temperatures up to 1300 0 C even though heating above approx. 700 0 C altered the alumino-silicate framework. However, some of the iodine appeared to be present as soluble iodine, even in heated materials. Treatment at 200 0 C in deionized water or 2M NaCl significantly decreased the crystallinity of the aluminosilicate framework and the α-AgI reflections in the x-ray patterns were enhanced. Mild γ irradiations (approx. 50 MR) affected the x-ray diffraction patterns of some of the zeolites. Various lead oxyhalides had very poor thermal stability

Inorganic-organic hybrid structure: Synthesis, structure and magnetic properties of a cobalt phosphite-oxalate, [C4N2H12][Co4(HPO3)2(C2O4)3

International Nuclear Information System (INIS)

Mandal, Sukhendu; Natarajan, Srinivasan

2005-01-01

A hydrothermal reaction of a mixture of cobalt (II) oxalate, phosphorous acid, piperazine and water at 150 o C for 96h followed by heating at 180 o C for 24h gave rise to a new inorganic-organic hybrid solid, [C 4 N 2 H 12 ][Co 4 (HPO 3 ) 2 (C 2 O 4 ) 3 ], I. The structure consists of edge-shared CoO 6 octahedra forming a [Co 2 O 10 ] dimers that are connected by HPO 3 and C 2 O 4 units forming a three-dimensional structure with one-dimensional channels. The amine molecules are positioned within these channels. The oxalate units have a dual role of connecting within the plane of the layer as well as out of the plane. Magnetic susceptibility measurement shows the compound orders antiferromagnetically at low temperature (T N =22K). Crystal data: I, monoclinic, space group=P2 1 /c (No. 14). a=7.614(15), b=7.514(14), c=17.750(3)A, β=97.351(3) o , V=1007.30(3)A 3 , Z=2, ρ calc =2.466g/cm 3 , μ (MoKα) =3.496mm -1 , R 1 =0.0310 and wR 2 =0.0807 data [I>2σ(I)

Radioecological reduction of acute and long-term environmental contamination with 129I

International Nuclear Information System (INIS)

Schuettelkopf, H.

1978-01-01

In the course of the research project 'Investigations on the radioecology of 129 I', analytical methods with extremely low detection limits for all important test materials have been developed. The behaviour of 129 I in a reprocessing plant and its emission from a reprocessing plant has been completely investigated and understood. The feared long-term hazard due to a single environmental contamination with 129 I is not to be expected as the biological availability of 129 I in the ground is reduced with a half-life of 0.3a. The 'basis for calculation' recommended by the Federal Minister of the Interior overestimate 129 I doses by at least a factor of 45. (orig.) [de

Using 14C and 3H to understand groundwater flow and recharge in an aquifer window

Science.gov (United States)

Atkinson, A. P.; Cartwright, I.; Gilfedder, B. S.; Cendón, D. I.; Unland, N. P.; Hofmann, H.

2014-12-01

Knowledge of groundwater residence times and recharge locations is vital to the sustainable management of groundwater resources. Here we investigate groundwater residence times and patterns of recharge in the Gellibrand Valley, southeast Australia, where outcropping aquifer sediments of the Eastern View Formation form an "aquifer window" that may receive diffuse recharge from rainfall and recharge from the Gellibrand River. To determine recharge patterns and groundwater flow paths, environmental isotopes (3H, 14C, δ13C, δ18O, δ2H) are used in conjunction with groundwater geochemistry and continuous monitoring of groundwater elevation and electrical conductivity. The water table fluctuates by 0.9 to 3.7 m annually, implying recharge rates of 90 and 372 mm yr-1. However, residence times of shallow (11 to 29 m) groundwater determined by 14C are between 100 and 10 000 years, 3H activities are negligible in most of the groundwater, and groundwater electrical conductivity remains constant over the period of study. Deeper groundwater with older 14C ages has lower δ18O values than younger, shallower groundwater, which is consistent with it being derived from greater altitudes. The combined geochemistry data indicate that local recharge from precipitation within the valley occurs through the aquifer window, however much of the groundwater in the Gellibrand Valley predominantly originates from the regional recharge zone, the Barongarook High. The Gellibrand Valley is a regional discharge zone with upward head gradients that limits local recharge to the upper 10 m of the aquifer. Additionally, the groundwater head gradients adjacent to the Gellibrand River are generally upwards, implying that it does not recharge the surrounding groundwater and has limited bank storage. 14C ages and Cl concentrations are well correlated and Cl concentrations may be used to provide a first-order estimate of groundwater residence times. Progressively lower chloride concentrations from 10

1,4-Iron Migration for Expedient Allene Annulations through Iron-Catalyzed C-H/N-H/C-O/C-H Functionalizations.

Science.gov (United States)

Mo, Jiayu; Müller, Thomas; Oliveira, João C A; Ackermann, Lutz

2018-06-25

C-H activation bears great potential for enabling sustainable molecular syntheses in a step- and atom-economical manner, with major advances having been realized with precious 4d and 5d transition metals. In contrast, we employed earth abundant, nontoxic iron catalysts for versatile allene annulations through a unique C-H/N-H/C-O/C-H functionalization sequence. The powerful iron catalysis occurred under external-oxidant-free conditions even at room temperature, while detailed mechanistic studies revealed an unprecedented 1,4-iron migration regime for facile C-H activations. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Application of the efficiency tracing method to the liquid scintillation metrology of 3H and 14C dual-labelled samples; Aplicacion del metodo de la figura de merito a la metrologia por centelleo liquido de muestras doblemente marcadas con 3H y 14C.

Energy Technology Data Exchange (ETDEWEB)

Martin-Casallo, M. T.; Los Arcos, J. M.; Grau, A.

1989-07-01

Two calculation procedures have been tested for the application of the efficiency tracing method to the activity determination of 3H and 14C dual- -labelled samples in the liquid scintillation metrology. A procedure Ieads to the statement of a linear equations system as a function of the quenching parameter, while the other one uses a least-square algorithm to fit the total count rate against the quenching parameter. The first procedure is strongly sensitive to the statistical uncertainty on the partial efficiencies and produces discrepancies which may reach more than 100% compared to the real values. The second procedure leads to more reliable results, showing discrepancies between 0.1% and 0.6% for the 3H activity and between 0.6% and 5% for the 14C activity, as that the efficiency tracing method can be applied to the metro- logy of dual-labelled samples of 3H and 14C by means of this procedure. (Author) 7 refs.

New homo- and heteroleptic derivatives of trivalent ytterbium containing anion-radical 1,4-diazadiene ligands. Synthesis, properties and crystal structure of (C9H7)2Yb[2-MeC6H4NC(Me)C(Me)NC6H4Me-2] and [PhNC(Ph)C(Ph)NPh]3Yb complexes

International Nuclear Information System (INIS)

Gudilenkov, I.D.; Fukin, G.K.; Cherkasov, A.V.; Shavyrin, A.S.; Trifonov, A.A.; Larionova, Yu.E.

2008-01-01

Reaction of ytterbium bisindenyl complex (C 9 H 7 ) 2 Yb II (THF) 2 (1) with 1,4-diazabutadiene 2-MeC 6 H 4 N=C(Me)-C(Me)=NC 6 H 4 Me-2 ( Me DAD) is accompanied by the oxidation of metal atom until trivalent state and results in the formation of paramagnetic compound of metallocenes type (C 9 H 7 ) 2 Yb III ( Me DAD -. ) (3) containing 1,4-diazabutadiene anion-radical. Structure of complex 3 is ascertained by the X-ray structure analysis. Reactions of bisindenyl (1) and bisfluorenyl (C 13 H 9 ) 2 Yb II (THF) 2 (2) derivatives of bivalent ytterbium with 1,4-diazabutadiene PhN=C(Ph)-C(Ph)=NPh ( Ph DAD) (at 1:2 molar ratio of reagents) proceed with the complete break of Yb-C bonds, oxidation of ytterbium atom until trivalent state, and result in the formation of homoligand complex ( Ph DAD -. ) 3 Yb (6) containing three anion-radical 1,4-diazadiene ligands. Complex 6 was also prepared by the exchange reaction of YbCl 3 with Ph DAD -. K + (1:3) in THF. Complex 6 is characterized by the X-ray structure analysis [ru

Optical spectroscopy of two-dimensional layered (C(6)H(5)C(2)H(4)-NH(3))(2)-PbI(4) perovskite.

Science.gov (United States)

Gauthron, K; Lauret, J-S; Doyennette, L; Lanty, G; Al Choueiry, A; Zhang, S J; Brehier, A; Largeau, L; Mauguin, O; Bloch, J; Deleporte, E

2010-03-15

We report on optical spectroscopy (photoluminescence and photoluminescence excitation) on two-dimensional self-organized layers of (C(6)H(5)C(2)H(4)-NH(3))(2)-PbI(4) perovskite. Temperature and excitation power dependance of the optical spectra gives a new insight into the excitonic and the phononic properties of this hybrid organic/inorganic semiconductor. In particular, exciton-phonon interaction is found to be more than one order of magnitude higher than in GaAs QWs. As a result, photoluminescence emission lines have to be interpreted in the framework of a polaron model.

Condensation time of the solar nebula from extinct I-129 in primitive meteorites

Science.gov (United States)

Lewis, R. S.; Anders, E.

1975-01-01

Mineral separates from five carbonaceous chondrites were dated by extinct 16 million year I-129, in an attempt to establish the condensation time of the solar nebula. Two Fe3O4 or Fe3O4-FeS samples from the Murchison and Orgueil meteorites are older than any other material dated thus far, and apparently formed within 200,000 years of each other. The great age, close isochronism, and primitive nature of the samples suggest that the event recorded was the condensation stage of the solar nebula. It provides a suitable zero point for the chronology of the early solar system. The I-129/I-127 ratio during condensation of the nebula was (1.46 plus or minus 0.04) times 0.0001. The recrystallized C4 chondrite Karoonda began to retain Xe-129 1.8 plus or minus 0.5 million years after the above event. This short cooling time implies rapid accretion (not exceeding 1 million years) and a shallow origin (not exceeding 10 km) below the surface of its parent body.-

Condensation time of the solar nebula from extinct 129I in primitive meteorites

International Nuclear Information System (INIS)

Lewis, R.S.; Anders, E.

1975-01-01

Mineral separates from five carbonaceous chondrites were dated by extinct 16 million year 129 I, in an attempt to establish the condensation time of the solar nebula. Two Fe 3 O 4 or Fe 3 O 4 --FeS samples from the Murchison and Orgueil meteorites are older than any other material dated thus far, and apparently formed within 2 x 10 5 years of each other. The great age, close isochronism, and primitive nature of the samples suggest that the event recorded was the condensation stage of the solar nebula. It provides a suitable zero point for the chronology of the early solar system. The 129 I/ 127 I ratio during condensation of the nebula was (1.46 +- 0.04) x 10 -4 . The recrystallized C4 chondrite Karoonda began to retain 129 Xe 1.8 +- 0.5 million years after the above event. This short cooling time implies rapid accretion (less than or equal to 1 million years) and a shallow origin (less than or equal to 10 km) below the surface of its parent body. (U.S.)

Application of the efficiency tracing method to the liquid scintillation metrology of 3H and 14C dual-labelled samples

International Nuclear Information System (INIS)

Martin-Casallo, M. T.; Los Arcos, J. M.; Grau, A.

1989-01-01

Two calculation procedures have been tested for the application of the efficiency tracing method to the activity determination of 3H and 14C dual- -labelled samples in the liquid scintillation metrology. A procedure Ieads to the statement of a linear equations system as a function of the quenching parameter, while the other one uses a least-square algorithm to fit the total count rate against the quenching parameter. The first procedure is strongly sensitive to the statistical uncertainty on the partial efficiencies and produces discrepancies which may reach more than 100% compared to the real values. The second procedure leads to more reliable results, showing discrepancies between 0.1% and 0.6% for the 3H activity and between 0.6% and 5% for the 14C activity, as that the efficiency tracing method can be applied to the metro- logy of dual-labelled samples of 3H and 14C by means of this procedure. (Author) 7 refs

Molecular and crystal structure of nido-9-C5H5N-11-I-7,8-C2B9H10: supramolecular architecture via hydrogen bonding X-H...I (X = B, C)

International Nuclear Information System (INIS)

Polyanskaya, T.M.

2006-01-01

A monocrystal X-ray diffraction study of a new iodine-containing cluster compound 9-(pyridine)-11-iodo-decahydro-7,8-dicarba-nido-undecaborane [9-C 5 H 5 N-11-I-7,8-C 2 B 9 H 10 ] has been performed. Crystal data: C 7 H 15 B 9 NI, M = 337.39, monoclinic, space group P2 1 /c, unit cell parameters: a=9.348(1) A, b=11.159(1) A, c=13.442(2) A, β=98.13(1) deg, V=1388.1(5) A 3 , Z=4, d calc = 1.614 g/cm 3 , T = 295 K, F(000)=648, μ=2.276 mm -1 . The structure was solved by a direct method and refined in the full-matrix anisotropic approximation (isotropic for hydrogen atoms) to final agreement factors R 1 = 0.0254, wR 2 = 0.0454 for 2437 I hkl >2σ I from 3590 measured I hkl (an Enraf-Nonius CAD-4 diffractometer, λMoK α , graphite monochromator, θ/2θ-scanning). The molecules are joined into a supramolecular assembly by hydrogen bonds X-H...I (X = B, C) [ru

Influence of pH on the /sup 14/C-labelling pattern after photosynthesis of suspended leaf slices and isolated mesophyll cells from chenopodium album in NaH/sup 14/CO/sub 3/

Energy Technology Data Exchange (ETDEWEB)

Baumann, G; Guenther, G [Paedagogische Hochschule Karl Liebknecht, Potsdam (German Democratic Republic). Sektion Chemie/Biologie

1983-01-01

Photosynthetic fixation of /sup 14/C from solutions of NaH/sup 14/CO/sub 3/ (at constant concentrations of free CO/sub 2/) by suspended leaf slices or isolated mesophyll cells from Chenopodium album is increased with increasing pH. Above all, the incorporation of radioactivity into amino acids and malate is stimulated. A direct uptake of HCO/sub 3/ ions and its fixation by PEP carboxylase is suggested. Isolated mesophyll cells showed at pH 7.3 a higher rate of photosynthesis than at pH 5.0.

The 129iodine bomb pulse recorded in Mississippi River Delta sediments: results from isotopes of I, Pu, Cs, Pb, and C

Science.gov (United States)

Oktay, S. D.; Santschi, P. H.; Moran, J. E.; Sharma, P.

2000-03-01

129I ( t1/2 = 1.56 × 10 7 yr) has both natural as well as anthropogenic sources. Anthropogenic sources from nuclear reprocessing discharges and bomb test fallout have completely overwhelmed the natural signal on the surface of the earth in the last 50 years. However, the transfer functions in and out of environmental compartments are not well known due to temporal variations in the sources of 129I and to a lack of knowledge regarding the forms of iodine. From a vertical profile of 129I/ 127I ratios in sediments located in the Mississippi Delta region in approximately 60 meters water depth, the 129I input function to this region was reconstructed. Dates in the core were assigned based on the plutonium peak at 20 cm depth (assumed to have been deposited in 1963) and the excess 210Pb profile in the same depth interval, and below that, based on the steadily decreasing 240Pu/ 239Pu ratios from a ratio of 0.18 at 22 cm to 0.05 at 57 cm depth, the 1953 horizon. These low 240Pu/ 239Pu values are attributed to low yield, close-in, tropospherically transported bomb fallout produced from the Nevada test site in the early 1950s, which had a value of about 0.035, and strongly suggest a terrestrial source for Pu isotopes. 129I/ 127I ratios increased from 2 × 10 -10 at 3 cm to 4 × 10 -10 at 20 cm, and from there decreased monotonously to pre-anthropogenic values at 53 cm and below. 129I concentrations ranged from 8-13 × 10 6 atoms/g in the top 20 cm, and decreased to values of less than 1 × 10 6 atoms/g below 50 cm. Atom ratios of 129I/ 137Cs, decay corrected to 1962, the year of maximum radionuclide production, are about 0.3, very close to the production ratios of about 0.2 during atomic bomb tests. This evidence, combined with other observations, strongly suggests that 129I in Mississippi River Delta sediments originates from atomic bomb fallout eroded from soils of the Mississippi River drainage basin, with little alteration of the isotopic ratios during transport from

Reconstructing surface ocean circulation with 129I time series records from corals.

Science.gov (United States)

Chang, Ching-Chih; Burr, George S; Jull, A J Timothy; Russell, Joellen L; Biddulph, Dana; White, Lara; Prouty, Nancy G; Chen, Yue-Gau; Shen, Chuan-Chou; Zhou, Weijian; Lam, Doan Dinh

2016-12-01

The long-lived radionuclide 129 I (half-life: 15.7 × 10 6  yr) is well-known as a useful environmental tracer. At present, the global 129 I in surface water is about 1-2 orders of magnitude higher than pre-1960 levels. Since the 1990s, anthropogenic 129 I produced from industrial nuclear fuels reprocessing plants has been the primary source of 129 I in marine surface waters of the Atlantic and around the globe. Here we present four coral 129 I time series records from: 1) Con Dao and 2) Xisha Islands, the South China Sea, 3) Rabaul, Papua New Guinea and 4) Guam. The Con Dao coral 129 I record features a sudden increase in 129 I in 1959. The Xisha coral shows similar peak values for 129 I as the Con Dao coral, punctuated by distinct low values, likely due to the upwelling in the central South China Sea. The Rabaul coral features much more gradual 129 I increases in the 1970s, similar to a published record from the Solomon Islands. The Guam coral 129 I record contains the largest measured values for any site, with two large peaks, in 1955 and 1959. Nuclear weapons testing was the primary 129 I source in the Western Pacific in the latter part of the 20th Century, notably from testing in the Marshall Islands. The Guam 1955 peak and Con Dao 1959 increases are likely from the 1954 Castle Bravo test, and the Operation Hardtack I test is the most likely source of the 1959 peak observed at Guam. Radiogenic iodine found in coral was carried primarily through surface ocean currents. The coral 129 I time series data provide a broad picture of the surface distribution and depth penetration of 129 I in the Pacific Ocean over the past 60 years. Copyright © 2016 The Authors. Published by Elsevier Ltd.. All rights reserved.

Studies on 14C-extractable residue, 14C-bound residue and mineralization of 14C-labeled chlorsulfuron in soils

International Nuclear Information System (INIS)

Ye Qingfu; Sun Jinhe; Qi Wenyuan; Wu Jianmin

2003-01-01

The purpose of the present study was to investigate 14 C-extractable residue ( 14 C-ER), 14 C-bound residue ( 14 C-BR) and mineralization of 14 C-labeled chlorsulfuron in soils by using isotope technique. The main factors affecting 14 C-BR formation and the distribution pattern of 14 C-BR in humus were also discussed in details. The results were as follows: (1) The 14 C-ER content of 14 C-chlorsulfuron in seven kinds of soil was positively related to soil pH and negatively related to clay content and organic matter content significantly. Moreover. the decrease rate of 14 C-chlorsulfuron parent compound derived from 14 C-ER in soils followed the first order rate reaction, the half-life in Soil 1-Soil 7 were 13.0, 13.1, 17.7, 133.3, 21.8, 22.1, 33.2 days, respectively. It was concluded that soil pH was the main factor affecting the degradation of 14 C-chlorsulfuron. (2) The 14 C-BR content of 14 C-chlorsulfuron in soils increased sharply with the incubation time during the initial 20 days, then changed slowly with time. However, 14 C-BR content during the whole incubation depended on soil types. The order of 14 C-BR content followed Soil 1 > Soil 2, Soil 5 and Soil 6 > Soil 3 > Soil 7 > Soil 4. The maximum values of 14 C-BR content of 14 C-chlorsulfuron in Soil 1-Soil 7 were 53.3%, 40.9%, 37.8%, 16.4%, 42.5%, 41.0% and 31.3% of applied amount. In addition, the 14 C-BR content of 14 C-chlorsulfuron in soils was negatively related to soil pH significantly, and positively related to the clay content. The soil pH was found to be the main factor affecting BR formation of 14 C-chlorsulfuron among the basic properties of soil. (3) During the whole periods of the incubation, the 14 C-BR of 14 C-chlorsulfuron in soils was mainly distributed in fulvic acid and humin. The relative percent of 14 C-BR in fulvic acid was higher than in humin. While the relative percentage of the 14 C-BR in humic acid only account for 2%. It was suggested that fulvic acid played an important role

Synthesis of methyl 3-O-{alpha}-d-glucopyranosyl-C{sub 6}{sup 14}-{beta}-d-xylopyranoside and methyl 2-O-{alpha}-d-Glucopyranosyl-C{sub 6}{sup 14}-l-noviopyranoside; Synthese de methyl-3-O-alpha-D-glucopyranosyl-C{sup 14}-beta-D-xylophranoside et methyl-2-O-alpha-D-glucopyranosyl-C{sub 6}{sup 14}-L-noviopyranoside; Sintez metil-3-O-{alpha}-D-glyukopiranozila-C{sub 6}{sup 14}-{beta}-D-ksilopiranozid i metil 2-O-{alpha}-D-glyukopiranozil-C{sub 6}{sup 14}-L-noviopiranozid; Sintesis de la metil 3-O-{alpha}-D-glucopiranosil-{sup 14}C{sub 6}-{beta}-D-xilopiranosido y de la metil 2-O-{alpha}-D-glucopiranosil-{sup 14}C{sub 6}-L-noviopiranosido

Energy Technology Data Exchange (ETDEWEB)

Barker, S A; Keith, M C; Stacey, M; Stroud, D B.E. [Chemistry Department, University of Birmingham (United Kingdom)

1962-03-15

Where difficulty is encountered in the chemical synthesis of a disaccharide glycoside labelled with C{sub 6}{sup 14} specifically in only one of its sugar moieties it is often convenient to resort to a synthesis catalysed by microbial transglycosylases. Two examples of the application of this technique are reported; the syntheses: Maltose-C{sub 12}{sup 14} + Methyl {beta}-d-xylopyranoside Penicillium lilacinum/transglucosylase {yields} Methyl 3-0-{alpha}-d-Glucopyranosyl-C{sub 6}{sup 14}-{beta}-d-xylopyranoside (I) + Glucose-C{sub 6}{sup 14} Maltose-C{sub 12}{sup 14} + Methyl l-noviopyranoside Fusarium moniliforme/transglucosylase Methyl-2-0-{alpha}d-Glucopyranosyl-C{sub 6}{sup 14}-l-noviopyranoside (II) + Glucose-C{sub 6}{sup 14}. In such syntheses, it is predictable that the anomeric character of the glycosidic linkage of the donor disaccharide will be retained in the disaccharide synthezised and that the glycosyl residue transferred will be attached, through its reducing group, to the receptor monosaccharide glycoside. By using either a C{sup 14}-labelled donor disaccharide or a C{sup 14}-labelled receptor glycoside, a disaccharide can be synthesized with only one of its sugar moieties labelled. In the synthesis of II the only hydroxyl group free in the receptor methyl novioside is on C{sub 2} and the transferred glucosyl residue can only be attached here. In the synthesis of I the methyl xyloside has free hydroxyls on C{sub 2}, C{sub 3} and C{sub 4} and the microbial enzyme has been found to transfer the glucosyl residue specifically to the hydroxyl on C{sub 3}. The structures of I and I I have been established by the results of elemental analysis, optical rotation, infrared spectra together with an examination of the products of acid hydrolysis and periodate oxidation. (author) [French] Lorsqu'on se heurte a des difficultes dans la synthese chimique d'un glucoside de disaccharide marque au carbone-14 specifiquement dans un seul des deux sucres qui le

129I/127I ratios in Scottish coastal surface sea water: Geographical and temporal responses to changing emissions

International Nuclear Information System (INIS)

Schnabel, Christoph; Olive, Valerie; Atarashi-Andoh, Mariko; Dougans, Andrew; Ellam, Robert M.; Freeman, Stewart; Maden, Colin; Stocker, Martin; Synal, Hans-Arno; Wacker, Lukas; Xu Sheng

2007-01-01

This work constitutes the first survey of I isotope ratios for Scottish sea water including the first data for the west of Scotland. These data are of importance because of the proximity to the world's second largest emission source of 129 I to the sea, the Sellafield nuclear reprocessing plant, because of the increasing importance of the sea to land transfer of 129 I and also as input data for dose estimates based on this pathway of 129 I. 129 I/ 127 I ratios in SW Scotland reached 3 x 10 -6 in 2004. No strong variation of I isotope ratios was found from 2003 to 2005 in Scottish sea waters. Iodine isotope ratios increased by about a factor of 6 from 1992 to 2003 in NE Scotland, in agreement with the increase of liquid 129 I emissions from Sellafield over that time period. It is demonstrated that 129 I/ 127 I ratios agree better than 129 I concentrations for samples from similar locations taken in very close temporal proximity, indicating that this ratio is more appropriate to interpret than the radionuclide concentration

RLE (Research Laboratory of Electronics) Progress Report Number 129.

Science.gov (United States)

1987-01-01

27709 ELEMENT NO. NO. NO. NO. 1. TITLE finciade SeciantV Ciiiiiiificationt Progress Report.No. 129 12. PERSONAL AUTHORI(S) Jonathan Allen, Daniel...TMIS PAGE *~ ~ d 1 ". d4 ’V. ~a PI al . 1 AN *,.i **N %** RLE Progress Report No. 129 January 1987 Submitted by: Prof. Jonathan Allen Prof. Daniel...Clevenger, J. Floro, S.M. Garrison, J. Im, K. Ismail, H. Kahn, H.J. Kim, Y.C. Ku, J.C. Licini, U. Meirav, J.E. Palmer, S.L. Park, H.M. Quek , J. Scott

Iodine (I-129 and I-127) in aerosols from northern Europe

DEFF Research Database (Denmark)

Englund, E.; Aldahan, A.; Hou, Xiaolin

2010-01-01

Huge amount of 129I has been emitted to the environment during the last decades from a variety of anthropogenic nuclear activities. Aerosols represent a carrier of iodine in the atmosphere in addition to gaseous forms for which data are lacking in Sweden. In this study the first time series...... of iodine isotopes (129I and 127I) in aerosols covering the period of 1983 to 2008 from two sites in Sweden are presented. The results show that both 129I and 127I concentrations are considerably higher in southern compared to northern Sweden. Furthermore there is a significant difference in the relative...

Estimating permissible /sup 129/I-emission rates

Energy Technology Data Exchange (ETDEWEB)

Huebschmann, W G

1976-06-01

A mathematical method of iodine release limitation is presented which, in assessing the radiological effectiveness of /sup 129/I, takes advantage of the fact that the chemical behaviour of /sup 129/I resembles that of /sup 131/I and relies on the already extensive knowledge of the chemical and biological behaviour of /sup 131/I. If this method is used for calculating permissible /sup 129/I emission rates it is stated that no unnecessary restrictions need be imposed on a fuel reprocessing plant and that the grazing season for the pasture-cow-milk pathway can be taken into account. The concept is currently in use at the Karlsruhe Nuclear Research Center and seems to be appropriate for licensing of nuclear fuel reprocessing plants.

Is it necessary to transmute 129I?

International Nuclear Information System (INIS)

Nifenecker, H.; Brissot, R.

2001-01-01

129 I is the unstable fission product with the record half life of 15.7 million years. It is produced with a yield of 0.7% in the thermal neutron induced fission of 235 U. Typically, a 1 GWe PWR reactor produces about 4 kg of 129 I annually. Iodine is highly soluble in water, and that property compounded with its very long half life makes 129 I the isotope most likely to leak through the biosphere from a deep underground storage site. In fact it is highly probable that it will be incorporated in the biosphere before it decays. Therefore, at least for the far future, sequestration in deep underground sites is no more justified than direct and immediate dispersion into the environment. It is, thus, important to know at which level of deployment of nuclear power the diffusion of 129 I in the biosphere might be a hazard for living beings at any time in the future. (authors)

The synthesis of [[sup 2]H],[[sup 3]H], and [[sup 14]C]-labeled 8[beta]-[(methylthio)methyl]-6-propylergoline mesylate (pergolide mesylate), a potent, long-acting dopamine agonist

Energy Technology Data Exchange (ETDEWEB)

Wheeler, W.J.; Kau, D.L.K.; Bach, N.J. (Lilly (Eli) and Co., Indianapolis, IN (United States). Lilly Research Labs.)

1990-03-01

The [[sup 3]H]- and two[[sup 14]C]-isopomers of 8[beta]-[(methylthio)methyl]-6-propylergoline mesylate (pergolide mesylate) have been synthesized. The [[sup 3]H]-derivative was synthesized by the palladium catalyzed tritiation of the corresponding 6-allyl derivative. Reaction of 8[beta]-[(methylthio)methyl]-ergoline with 1-[[sup 14]C]-1-propyl bromide yielded pergolide labeled in the 6-propyl group. Alternatively, reaction of 8[beta]-mesyloxy-6-propylergoline with [[sup 14]C]-sodium cyanide, followed by base hydrolysis, yielded 8 [beta]-carboxy-6-propylergoline-[[sup 14]C], which was subsequently converted to pergolide mesylate radiolabeled in the 17-position via a four step sequence. (Author).

Monitoring intervals for the measurement of the radionuclides 125I and 129I in the thyroid gland

International Nuclear Information System (INIS)

Yera Simanca, Yoan; Lopez Bejerano, Gladys M.; Ramos Machado, Dayana; Acosta Rodriguez; Nancy

2014-01-01

This paper shows the monitoring intervals that can be implemented in the Internal Contamination Laboratory of the Center for Radiation Protection and Hygiene for direct measurement of the radionuclides 125 I and 129 I in the Thyroid gland. Two measuring systems were used, one of them uses a scintillation detector and the other one uses a Phoswich detector. Both detectors were situated inside of one shielding chamber of 2.5 x 2.5 x 2.5 m of dimension, cover with 15 cm of steel, 3 mm of lead, 1.8 mm of tin, and 1.5 mm of copper. For each system was calculated the minimum detectable activity and in function of it were determined the monitoring intervals. The results obtained showed that for the radionuclide 125 I all the evaluated intervals (120, 90, 60, 30, 14 and 7 days).can be implemented with both systems. For the case of the radionuclide 129 I it can only be implemented the intervals (120, 90, and 60 days) using the scintillation detector and all of them with the Phoswich detector. (author)

Speciation and migration of 129I in soil profiles

DEFF Research Database (Denmark)

Luo, Maoyi; Hou, Xiaolin; Zhou, Weijian

2013-01-01

A method has been developed for speciation analysis of ultra low level 129I in soil using sequential extraction combined with coprecipitation for separation of carrier free iodine and AMS measurement of 129I. Two loess profiles collected from northwest China were analyzed for species of 129I...

Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography

International Nuclear Information System (INIS)

Laskey, R.A.; Mills, A.D.

1975-01-01

Methods which use the scintillator PPO to record film images of 3 H in chromatograms and polyacrylamide gels (fluorography) have been described elsewhere. This paper demonstrates that pre-exposure of the film to a brief flash of light greatly increases the sensitivity of fluorography. Pre-exposure also permits quantitative interpretation of the film image, because it corrects the non-linear relationship between redioactivity of the sample and absorbance of the film image. Therefore the distribution of radioactivity in the sample is accurately represented by micro-densitometry of the image obtained on pre-exposed film. Using pre-exposed film 300 dis. 3 H/min or 30 dis. 14 C/min can be detected in a band in a gel in a 24-h exposure. The appendix describes revisions and extensions of existing fluorographic procedures, including application to agarose gels and a rapid procedure for recovering PPO for re-use. (orig.) [de

Synthesis of (3,5-/sup 14/C)trachelanthamidine and (5-/sup 3/H)isoretronecanol and their incorporation into the retronecine moiety of riddelliine in Senecio riddellii

Energy Technology Data Exchange (ETDEWEB)

Leete, E.; Rana, J.

1986-09-01

(+/-)-(3,5-/sup 14/C)Trachelanthamidine and (+/-)-(5-/sup 3/H)isoretronecanol, which are diastereomers, were prepared from potassium (/sup 14/C)cyanide and (5-/sup 3/H)proline, respectively. These compounds and (1,4-/sup 14/C)putrescine were administered to Senecio riddellii plants resulting in the formation of labeled riddelliine, in which almost all the radioactivity was located in its retronecine moiety. The activity of the beta-alanine obtained by degradation of the retronecine was consistent with specific labeling of this pyrrolizidine base at the expected positions. The extremely high absolute incorporation (15.1, 22.1%) of trachelanthamidine into riddelliine strongly favors this 1-hydroxymethylpyrrolizidine as the one on the main biosynthetic pathway to retronecine. The lower incorporation (0.75%) of isoretronecanol may represent a minor or aberrant pathway to retronecine.

Specific primary ionization induced by minimum ionizing electrons in CH4, C2H6, C3H8, i-C4H10, Ar, DME,TEA and TMAE

International Nuclear Information System (INIS)

Melamud, G.; Breskin, A.; Chechik, R.; Pansky, A.

1992-10-01

Specific primary ionization induced by minimum ionizing electrons has been measured in several gases and vapors. Charges deposited by β-electrons in a low pressure gas, were collected, amplified by a multistep gaseous electron multiplier and counted. The high counting efficiency of the multiplier provided results of systematically higher values as compared to existing data. The respective values of the specific primary ionization in CH 4 C 2 H 6 , C 3 H 8 ,i-C 4 H 10 , Argon, Dimethylether, Triethylamine and Tetrakis(dimethylamino) ethylene are: 0.034, 0.065, 0.095, 0.12, 0.03, 0.082, 0.0195 and 0.370 clusters/cm*Torr. We present the experimental method and discuss the results and their accuracy. (authors)

Incineration and monitoring of low-level 3H and 14C wastes at a biological research institution

International Nuclear Information System (INIS)

Hamrick, P.E.; Knapp, S.J.; Parker, M.G.; Watson, J.E. Jr.

1986-01-01

Low-level radioactive waste containing liquid scintillation fluid and known amounts of 14 C and 3 H has been incinerated in a modified pathological incinerator with the incinerator effluent, refractory surface and ash being monitored. The study relates the activity monitored to that incinerated and discusses how this relation was affected by a modification of the incinerator and monitoring conditions. No significant activity was found to be associated with the ash, particulates or the refractory surface. These data suggest that most of the activity is released as tritiated water vapor and 14 C-labeled carbon dioxide. However, incomplete oxidation may occur for short periods of time depending on the amount of liquid scintillation fluid incinerated, with the possible release of 14 C-labeled carbon monoxide

129I/127I ratios in surface waters of the English Lake District

International Nuclear Information System (INIS)

Atarashi-Andoh, M.; Schnabel, C.; Cook, G.; MacKenzie, A.B.; Dougans, A.; Ellam, R.M.; Freeman, S.; Maden, C.; Olive, V.; Synal, H.-A.; Xu, S.

2007-01-01

Accelerator Mass Spectrometry (AMS) was used to measure 129 I/ 127 I ratios in surface sea, lake, and river water samples collected in 2004 and 2005 from the English Lake District and from SW Scotland, areas which are in relatively close proximity to the Sellafield nuclear fuel reprocessing plant in NW England. The 129 I/ 127 I ratios in surface water collected from the shore of the Irish Sea were in the range 2.8 x 10 -6 to 8.2 x 10 -6 . These ratios are one order of magnitude higher than that of seawater collected from the Irish Sea in 1992, correlating with the increase in 129 I content of the Sellafield liquid effluent discharge over the last decade. The 129 I/ 127 I ratios in lakes in the Lake District were in the range 0.7 x 10 -6 to 6.4 x 10 -6 and decreased exponentially as a function of distance from Sellafield. Consideration of the relative variation of stable I concentrations and 129 I/ 127 I ratios suggests that Sellafield gaseous discharges may be the dominant source of 129 I to the lakes

Liquid scintillation measurements of aqueous 14C or 3H containing samples in a toluene cocktail

International Nuclear Information System (INIS)

Engelmann, A.; Reinhard, G.

1980-01-01

On the basis of investigations of the ternary system toluene/methanol/water that composition of toluene/methanol scintillation cocktails has been determined, which allows liquid scintillation measurements of 14 C or 3 H containing samples in homogeneous distribution. Because of more pronounced quenching the optimum sample quantity was less for blood solutions extracted with a HClO 4 /H 2 O 2 mixture than for water. The effect of beta radiation energy has to be taken into account. (author)

Ratio of extinction to reddening for interstellar matter using galaxies. I. A limit on the neutral extinction from photometry of the 3C 129 group

International Nuclear Information System (INIS)

Sandage, A.

1975-01-01

The ratio of total extinction to reddening of interstellar matter has been determined by a new method applied to galaxies in the highly obscured 3C 129 and 3C 129.1 group (l = 160 0 , b = 0 0 ). The difference between the observed magnitude of the first-ranked group member and the magnitude calculated from the redshift-apparent magnitude (Hubble) diagram (at the known redshift of the group) is the total extinction A/sub v/ to within the sigma(M/sub v/) that applies to the first-ranked cluster member. Comparison of the observed color with the known intrinsic color of giant E galaxies gives E(B--V), and therefore R. Photometry of the 3C 129 group gives R identical with A/sub v//E(B--V) = 3.72 +- 0.32(sigma). Correction for the finite bandwidth of the BV system gives R (O star base) = 3.35 +- 0.29 (sigma). Comparison with R determined from the color-difference method gives a limit for the fraction of neutral-to-selective extinction of f = A/sub v/ (neutral)/A/sub v/ (selective) = 0.10 +- 0.15(sigma) which is a null result (f = 0) to within the statistics. Hence, no neutral extinction has been detected at the 1 sigma level of the experiment. Use of the method on many additional groups of galaxies is expected to substantially reduce the error of this limit

The measurement of I-129 in the Canadian Arctic basin and other Arctic waters

International Nuclear Information System (INIS)

Kilius, L.R.; Zhao, X.L.

1995-01-01

Since the first demonstration by accelerator mass spectrometry for the measurement of 129 I in oceanic systems, the use of 129 I as a long range tracer has become widespread because the constraint of large sample volumes has been removed. Following extensive measurements of 129 I in both the Barents and Kara Seas, seawater samples were collected within the Canadian Arctic Basin, and at a cruise from the Chuchi Sea, across the pole, to the Norwegian Sea. Only 450 ml samples were required for all AMS measurements of Arctic seawater. Enhanced concentrations of 129 I were observed. Based on 137 Cs measurements for the same samples, the 129 I/ 137 Cs ratios showed the signature of Sellafield reprocessing effluents as the primary source of this 129 I. Based on average estimates, 13% of the total Sellafield/La Hague 129 I emissions now resides within the Atlantic layer of the Arctic Ocean. 7 refs., 3 figs

Synthesis of both sup 14 C- and sup 3 H- labelled trospectomycin and the assessment of their utility in biological studies

Energy Technology Data Exchange (ETDEWEB)

Constable, D A; Dring, L G [Upjohn Ltd., Crawley (UK); Jones, J R [Surrey Univ., Guildford (UK). Dept. of Chemistry

1990-07-01

Three radiolabelled forms of trospectomycin (6'-n-propylspectinomycin sulphate hydrate) have been synthesised, namely (8'-{sup 14}C)-, (6',7'-{sup 3}H)-, and (5',6',7'-{sup 3}H)-trospectomycin. Although all three forms of the drug are metabolically stable and therefore suitable for use in animal studies the {sup 14}C compound is produced in poor yield as is the (6',7'-{sup 3}H)trospectomycin. On the other hand, the (5',6',7'-{sup 3}H)-form is produced in good yield and appears to be the labelled form of choice. Following subcutaneous administration of any of the labelled forms to rats, more than 50% of the dose was excreted in the urine as unchanged drug during the first 6h after dosing. Approximately 80% and 10% of the dose appeared in the urine and faeces respectively after 6 days. (author).

Synthesis of the mevalonic acid labelled with "1"4C, "1"3C and "3H

International Nuclear Information System (INIS)

Rousseau, Bernard

1982-01-01

This thesis describes five new methods of synthesis of the (R,S) mevalonic acid adapted to the labelling with "1"4C and "1"3C in positions 4,5 or 5 or 3', or with tritium in position 3'. Three of them use the tri-oxa-2,4,10 adamantyl group as masked carboxyl function. The two others take benefit from the regioselectivity of the bis-hydro-boration of terminal acetylenics by the 9-borabicyclo [3-3-1]nonane. The acylation of the bis-trimethylsilyl lithiomalonate, and the chemistry of dithiannes are also involved. Acetylene and methyl iodide labelled with isotopes are used as cheap base products [fr

H i Absorption in the Steep-Spectrum Superluminal Quasar 3C 216.

Science.gov (United States)

Pihlström; Vermeulen; Taylor; Conway

1999-11-01

The search for H i absorption in strong compact steep-spectrum sources is a natural way to probe the neutral gas contents in young radio sources. In turn, this may provide information about the evolution of powerful radio sources. The recently improved capabilities of the Westerbork Synthesis Radio Telescope have made it possible to detect a 0.31% (19 mJy) deep neutral atomic hydrogen absorption line associated with the steep-spectrum superluminal quasar 3C 216. The redshift (z=0.67) of the source shifts the frequency of the 21 cm line down to the ultra-high-frequency (UHF) band (850 MHz). The exact location of the H i-absorbing gas remains to be determined by spectral line VLBI observations at 850 MHz. We cannot exclude that the gas might be extended on galactic scales, but we think it is more likely to be located in the central kiloparsec. Constraints from the lack of X-ray absorption probably rule out obscuration of the core region, and we argue that the most plausible site for the H i absorption is in the jet-cloud interaction observed in this source.

Study of the unimolecular decompositions of the (C3H6)+2 and (c-C3H6)+2 complexes

International Nuclear Information System (INIS)

Tzeng, W.; Ono, Y.; Linn, S.H.; Ng, C.Y.

1985-01-01

The major product channels identified in the unimolecular decompositions ofC 3 H + 6 xC 3 H 6 and c-C 3 H + 6 xc-C 3 H 6 in the total energy [neutral (C 3 H 6 ) 2 or (c-C 3 H 6 ) 2 heat of formation plus excitation energy] range of approx.230--450 kcal/mol are C 3 H + 7 +C 3 H 5 , C 4 H + 7 +C 2 H 5 , C 4 H + 8 +C 2 H 4 , and C 5 H + 9 +CH 3 . The measured appearance energy for C 4 H + 7 (9.54 +- 0.04 eV) from (C 3 H 6 ) 2 is equal to the thermochemical threshold for the formation of C 4 H + 7 +C 2 H 5 from (C 3 H 6 ) 2 , indicating that the exit potential energy barrier for the ion--molecule reaction C 3 H + 6 +C 3 H 6 →C 4 H + 7 +C 2 H 5 is negligible. There is evidence that the formations of C 4 H + 7 +C 2 H 4 +H from (C 3 H 6 ) + 2 and (c-C 3 H 6 ) + 2 also proceed with high probabilities when they are energetically allowed. The variations of the relative abundances for C 4 H + 7 ,C 4 H + 8 , and C 5 H + 9 from (C 3 H 6 ) + 2 and (c-C 3 H 6 ) + 2 as a function of ionizing photon energy are in qualitative agreement, suggesting that (C 3 H 6 ) + 2 and (c-C 3 H 6 ) + 2 rearrange to similar C 6 H + 12 isomers prior to fragmentation. The fact that C 6 H + 11 is found to be a primary ion from the unimolecular decomposition of (c-C 3 H 6 ) + 2 but not (C 3 H 6 ) + 2 supports the conclusion that the distribution of C 6 H + 12 collision complexes involved in the C 3 H + 6 +C 3 H 6 reactions is different from that in the cyclopropane ion--molecule reactions

Bis[μ-1,2-bis(1H-imidazol-1-ylmethylbenzene-κ2N3:N3′]disilver(I 3-carboxylato-4-hydroxybenzenesulfonate methanol solvate trihydrate

Directory of Open Access Journals (Sweden)

Hong-Mei Sun

2009-09-01

Full Text Available In the title compound, [Ag2(C14H14N42](C7H4O6S·CH3OH·3H2O, the complex dication has a binuclear structure in which each AgI ion is two-coordinated in a slightly distorted linear coordination geometry. The two AgI atoms are bridged by two 1,2-bis[(1H-imidazol-1-ylmethyl]benzene (IBI ligands, forming a 22-membered ring. In the dication, π–π interactions are observed between the imidazole rings with centroid–centroid distances of 3.472 (3 and 3.636 (3 Å. In the crystal, the uncoordinated water molecules, anions and methanol solvent molecules are linked into chains along the b axis by O—H...O hydrogen bonds. In addition, π–π interactions are observed between the benzene rings of the IBI ligands, with a centroid–centroid distance of 3.776 (2 Å. The sulfonate group is disordered over two orientations with occupancies of 0.676 (12 and 0.324 (12.

Selection of chemical forms of iodine for transmutation of 129I

International Nuclear Information System (INIS)

Shirasu, Yoshiro; Minato, Kazuo

2003-01-01

To select suitable chemical forms of iodine for the target for transmutation of 129 I, the properties of iodine compounds of NaI, MgI 2 , CaI 2 , CuI and Ca(IO 3 ) 2 were compared and the out-of-reactor heating experiments of the pellets of CuI and Ca(IO 3 ) 2 with the cladding materials were carried out. CuI and Ca(IO 3 ) 2 are not deliquescent but stable in the air, which is of great advantage to construction, operation and maintenance of the processing plants. The cladding with Cu metal liner could be compatible with CuI though the compatibility of the stainless steel with CuI is not good. Ca(IO 3 ) 2 should be deleted from the list of the candidate target materials for the transmutation of 129 I due to the severe chemical reaction with the cladding materials

The transport of 3H and 14C in phloem strands of Heracleum lanatum and polyester threads

International Nuclear Information System (INIS)

Hoddinott, J.; Gorham, P.R.

1976-01-01

Experiments are described which show a great similarity in the profiles of rapid movement of tritium after external application of 3 H 2 O to a small segment of a phloem strand of Heracleum lanatum and a water-soaked polyester thread. Efflux of rapidly transported tritium from phloem strands and polyester threads was also similar. No rapid movement of radioisotope from (U- 14 C)sucrose, (6,6'- 3 H)sucrose, or (6- 3 H)glucose along phloem strands was observed. A possible explanation for the rapid movement of tritium in terms of proton transfer is offered. It is concluded that the rapid movement of tritium in a phloem strand which occurs when 3 H 2 O is applied externally to a segment is an artifact and that no normal translocation is occurring. (author)

Three closely related (2E,2′E-3,3′-(1,4-phenylenebis[1-(methoxyphenylprop-2-en-1-ones]: supramolecular assemblies in one dimension mediated by hydrogen bonding and C—H...π interactions

Directory of Open Access Journals (Sweden)

Aijia Sim

2017-06-01

Full Text Available In the title compounds, (2E,2′E-3,3′-(1,4-phenylenebis[1-(2-methoxyphenylprop-2-en-1-one], C26H22O4 (I, (2E,2′E-3,3′-(1,4-phenylenebis[1-(3-methoxyphenylprop-2-en-1-one], C26H22O4 (II and (2E,2′E-3,3′-(1,4-phenylenebis[1-(3,4-dimethoxyphenylprop-2-en-1-one], C28H26O6 (III, the asymmetric unit consists of a half-molecule, completed by crystallographic inversion symmetry. The dihedral angles between the central and terminal benzene rings are 56.98 (8, 7.74 (7 and 7.73 (7° for (I, (II and (III, respectively. In the crystal of (I, molecules are linked by pairs of C—H...π interactions into chains running parallel to [101]. The packing for (II and (III, features inversion dimers linked by pairs of C—H...O hydrogen bonds, forming R22(16 and R22(14 ring motifs, respectively, as parts of [201] and [101] chains, respectively.

NQR and X-ray crystal structure studies of cadmium halide complexes: [C(NH2)3]CdI3 and [4-ClC6H5NH3]3CdBr5

International Nuclear Information System (INIS)

Gesing, Thorsten M.; Lork, Enno; Terao, Hiromitsu; Ishihara, Hideta

2016-01-01

The crystal structures of [C(NH 2 ) 3 ]CdI 3 (1) and [4-ClC 6 H 5 NH 3 ] 3 CdBr 5 (2) have been determined at 100 K: monoclinic, Cc, a = 828.75(3) pm, b = 1615.31(5) pm, c = 810.64(3) pm, and β = 106.5820(10) for 1; monoclinic, P2 1 /c, a = 1486.93(5) pm, b = 794.31(3) pm, c = 2290.59(7) pm, and β = 99.6830(10) for 2. The structure of 1 has an infinite chain of anions consisting of [CdI 4 ] tetrahedra sharing two corners. The structure of 2 has an infinite chain of anions consisting of [CdBr 6 ] octahedra sharing two corners in cis positions. In both structures, isolated cations are connected to the anion chains through weak hydrogen bonds Cd-X..H to result in three-dimensional network structures. In accordance with the crystal structures, three 127 I (m = ±1/2 <-> m = ±3/2), five 81 Br, and three 35 Cl nuclear quadrupole resonance (NQR) lines were observed for 1 and 2. The NQR spectra reflect the anion chain structures and their weak hydrogen bonds. The MO calculations of the models [Cd 5 I 16 ] 6- for 1 and [Cd 3 Br 16 ] 10- for 2 estimate only about half the values for the NQR frequencies but give accurate electric field gradient directions.

Determination of "1"2"9I using volatilization method and liquid scintillation spectrometry

International Nuclear Information System (INIS)

Remenec, Boris; Dulanska, Silvia; Horvathova, Bianka; Matel, Lubomir

2017-01-01

A simple and rapid separation method for "1"2"9I determination in radioactive waste samples was developed. Suitable conditions for iodine volatilization were tested. Iodine was trapped in 1.5 mol L"-"1 NaOH and precipitated as PdI_2·H_2O by addition of PdCl_2 with recoveries higher than 80%. The method was applied for analysis of contaminated soil, radioactive sludge, evaporator concentrate and heterogeneous waste samples from nuclear power plants in Slovak Republic. "1"2"9I was measured on liquid scintillation counter TRI CARB 2900 TR using Ultima Gold AB scintillation cocktail. (author)

Methodology for the determination of environmental 129I and 99Tc

International Nuclear Information System (INIS)

Anderson, T.J.

1978-01-01

The Savannah River Laboratory is using existing techniques and developing new methodology to determine the environmental impact of the Savannah River Plant with regard to 129 I and 99 Tc. 129 I is determined by neutron activation after the method of Brauer. Activation products are quantified by γ-ray spectroscopy [Ge(Li)] following chemical isolation. 125 I is used as a yield tracer. 129 I amounts as low as 3.8 fCi can be determined with 30-minute counting times. An isotope dilution method for 99 Tc based on a three-stage surface ionization mass spectrometer is being developed. Its chemical isolation scheme ends with the Tc loaded on a single ion-exchange bead for enhanced mass-spectrometric sensitivity. 97 Tc will be used as a yield tracer. A lower limit of 0.2 fCi is sought. A modified method using liquid scintillation counting has determined 99 Tc in some aqueous samples. These methods have confirmed that 129 I and 99 Tc can be highly mobile in the aqueous environment, establishing the need for monitoring

Analysis of ¹²⁹I and its Application as Environmental Tracer

DEFF Research Database (Denmark)

Hou, Xiaolin; Hou, Yingkun

2012-01-01

, and highlights the progress of these analytical methods for chemical separation and sensitive measurement of 129I. The naturally occurred 129I has been used for age dating of samples/events in a range of 2-80 Ma. For the purpose of this study, an initial value of 129I has to be measured. Some progress......Iodine-129, the long-lived radioisotope of iodine, occurs naturally, but anthropogenic generated 129I has dominated the environment in the past 60 years. Due to active chemical and environmental properties of iodine and the enhanced analytical capacity for 129I measurement, the application of 129I...

TRACING H2 COLUMN DENSITY WITH ATOMIC CARBON (C I) AND CO ISOTOPOLOGS

International Nuclear Information System (INIS)

Lo, N.; Bronfman, L.; Cunningham, M. R.; Jones, P. A.; Lowe, V.; Cortes, P. C.; Simon, R.; Fissel, L.; Novak, G.

2014-01-01

We present the first results of neutral carbon ([C I] 3 P 1 - 3 P 0 at 492 GHz) and carbon monoxide ( 13 CO, J = 1-0) mapping in the Vela Molecular Ridge cloud C (VMR-C) and the G333 giant molecular cloud complexes with the NANTEN2 and Mopra telescopes. For the four regions mapped in this work, we find that [C I] has very similar spectral emission profiles to 13 CO, with comparable line widths. We find that [C I] has an opacity of 0.1-1.3 across the mapped region while the [C I]/ 13 CO peak brightness temperature ratio is between 0.2 and 0.8. The [C I] column density is an order of magnitude lower than that of 13 CO. The H 2 column density derived from [C I] is comparable to values obtained from 12 CO. Our maps show that C I is preferentially detected in gas with low temperatures (below 20 K), which possibly explains the comparable H 2 column density calculated from both tracers (both C I and 12 CO underestimate column density), as a significant amount of the C I in the warmer gas is likely in the higher energy state transition ([C I] 3 P 2 - 3 P 1 at 810 GHz), and thus it is likely that observations of both the above [C I] transitions are needed in order to recover the total H 2 column density

Ingestion dose pathway parameters of H-3 and C-14 in Korea

Energy Technology Data Exchange (ETDEWEB)

Yang-Geun Chung; Gab-Bock Lee; Sun-Young Bang [Korea Electric Power Research Institute (Korea, Republic of); Seung-Ong Lee [Korea Hydro and Nuclear Power Cooperation (Korea, Republic of)

2006-07-01

Full text of publication follows: H-3 and C-14 are the main nuclides for public ingestion dose around nuclear power plants in Korea. Key parameters of H-3 and C-14 ingestion dose pathways are the fractions of moisture, hydrogen, and carbon in agricultural vegetation. In this study, representative values of the moisture, hydrogen, and carbon contents for categorized food groups were established. The food stuffs are classified into four groups such as grain, leafy vegetable, root vegetable, and fruit. Methods Weighting factors for individual food items were considered to calculate representative values of each food group using the 2001-2002 national dietary survey, published by the Ministry of Health and Welfare (MOHW). The weighting factor for individual food stuff was determined by the ratio of each food item to the total intake of each food group. Representative values of the moisture, hydrogen, and carbon contents for the four food groups were calculated using the annual weighting factor and the fractions of moisture, hydrogen, and carbon of individual food stuff based on the sixth revision of Food Composition Table published by the Rural Living Science Research Institute (RLSI). Results The weighting factor of rice in grain group was 95% on a yearly basis. Those of Chinese cabbage in leafy vegetable group and radish in root vegetable group were 58% and 52%, respectively. The fruit consumption varied with seasons. Annual weighting factors of apple, persimmon, water melon, and pear in fruit were 21%, 18%, 17%, and 15%, respectively. The respective fractions of moisture in grain, leafy vegetable, root vegetable, and fruit were 10.8%, 93.0%, 88.3%, and 88.0%: those of hydrogen were 5.6%, 0.4%, 0.7%, and 0.74%: those of carbon were 39.68%, 2.84%, 4.98%, and 5.23%. The hydrogen fraction of root vegetable was 75% larger than that of leafy vegetable. The values of moisture, hydrogen, and carbon contents in agricultural vegetation calculated from the Food Composition

Ingestion dose pathway parameters of H-3 and C-14 in Korea

International Nuclear Information System (INIS)

Yang-Geun Chung; Gab-Bock Lee; Sun-Young Bang; Seung-Ong Lee

2006-01-01

Full text of publication follows: H-3 and C-14 are the main nuclides for public ingestion dose around nuclear power plants in Korea. Key parameters of H-3 and C-14 ingestion dose pathways are the fractions of moisture, hydrogen, and carbon in agricultural vegetation. In this study, representative values of the moisture, hydrogen, and carbon contents for categorized food groups were established. The food stuffs are classified into four groups such as grain, leafy vegetable, root vegetable, and fruit. Methods Weighting factors for individual food items were considered to calculate representative values of each food group using the 2001-2002 national dietary survey, published by the Ministry of Health and Welfare (MOHW). The weighting factor for individual food stuff was determined by the ratio of each food item to the total intake of each food group. Representative values of the moisture, hydrogen, and carbon contents for the four food groups were calculated using the annual weighting factor and the fractions of moisture, hydrogen, and carbon of individual food stuff based on the sixth revision of Food Composition Table published by the Rural Living Science Research Institute (RLSI). Results The weighting factor of rice in grain group was 95% on a yearly basis. Those of Chinese cabbage in leafy vegetable group and radish in root vegetable group were 58% and 52%, respectively. The fruit consumption varied with seasons. Annual weighting factors of apple, persimmon, water melon, and pear in fruit were 21%, 18%, 17%, and 15%, respectively. The respective fractions of moisture in grain, leafy vegetable, root vegetable, and fruit were 10.8%, 93.0%, 88.3%, and 88.0%: those of hydrogen were 5.6%, 0.4%, 0.7%, and 0.74%: those of carbon were 39.68%, 2.84%, 4.98%, and 5.23%. The hydrogen fraction of root vegetable was 75% larger than that of leafy vegetable. The values of moisture, hydrogen, and carbon contents in agricultural vegetation calculated from the Food Composition

Triosmium cluster compounds containing isocyanide and hydride ligands. Crystal and molecular structures of (μ-H)(H)Os3(CO)10(CN-t-C4H9) and (μ-H)2Os3(CO)9(CN-t-C4H9)

International Nuclear Information System (INIS)

Adams, R.D.; Golembski, N.M.

1979-01-01

The structures of the compounds (μ-H)(H)Os 3 (CO) 10 (CN-t-C 4 H 9 ) and (μ-H) 2 Os 3 (CO) 9 (CN-t-C 4 H 9 ) have been revealed by x-ray crystallographic techniques. For (μ-H)(H)Os 3 (CO) 10 (CN-t-C 4 H 9 ): a = 9.064 (3), b = 12.225 (3), c = 20.364 (4) A; β = 98.73 (3) 0 ; space group P2 1 /c[C/sub 2h/ 5 ], No. 14; Z = 4; d/sub calcd/ = 2.79 g cm -3 . This compound contains a triangular cluster of three osmium atoms; Os(1)--Os(2) = 2.930 (1) A, Os(1)--Os(3) = 2.876 (1) A, and Os(2)--Os(3) = 3.000 (1) A. There are ten linear terminal carbonyl groups and one linear terminal isocyanide ligand which occupies an axial coordination site. The hydrogen atoms were not observed crystallographically, but their positions are strongly inferred from considerations of molecular geometry. For (μ-H) 2 Os 3 (CO) 9 (CN-t-C 4 H 9 ): a = 15.220 (8), b = 12.093 (6), c = 23.454 (5) A; space group Pbcn [D/sub 2h/ 14 ], No. 60; Z = 8; d/sub calcd/ = 2.79 g cm -3 . The compound is analogous to the parent carbonyl (μ-H) 2 Os 3 (CO) 10 and has two normal and one short osmium--osmium bonds: Os(1)--Os(2) = 2.827 (1) A, Os(1)--Os(3) = 2.828 (1) A, Os(2)--Os(3) = 2.691 (1) A. The isocyanide ligand resides in an equatorial coordination site on osmium Os(2). The hydrogen atoms were not observed but are believed to occupy bridging positions as in the parent carbonyl complex. 2 figures, 7 tables

Quantitation of some amino-terminal residues in proteins using 3H-labelled dansyl chloride and 14C labelled amino acids

International Nuclear Information System (INIS)

Flengsrud, R.

1979-01-01

A method for quantitation of amino-terminal residues in proteins is presented. The method is a modification of a double isotope-labelling technique, using 3 H-labelled dansyl chloride and 14 C-labelled amino acids as internal standards. The method is demonstrated on human fibrinogen, horse myoglobin and on mouse myoloma IgA. A linear relationship between the ratio 3 H/ 14 C in the separated amino-terminal amino acid of the protein and the amount of protein added in the labelling mixture was obtained with standard deviations of +- 7.4%, +-3.4% and +-10.3%, respectively. An application of the method is demonstrated by measuring the increase in amino-terminal glycine in fibrinogen following the proteolytic action of thrombin. The method seems to be useful when 0.1 nmol or more of protein is used. (author)

Primary assimilation process of triply (/sup 15/N, /sup 14/C and /sup 3/H) labeled arginine in the roots of arginine-fed barley

Energy Technology Data Exchange (ETDEWEB)

Mori, Satoshi [Tokyo Univ. (Japan). Faculty of Agriculture

1981-03-01

To clarify the mechanism of arginine utilization in barley roots, triply labeled (ureido-/sup 15/N, ureido-/sup 14/C and 5-/sup 3/H) arginine was applied to plants precultured with arginine (Arg-plants). (5-/sup 3/H) Arginine was incorporated mainly into ornithine, suggesting that arginase contributes in the first step of arginine metabolism. The arginase activity in the tissues was greatly enhanced by continuous supply of arginine, whereas urease activity was not by the same treatment. The amount of /sup 14/CO/sub 2/ evolved from (ureido-/sup 14/C) arginine in the Arg-plants was several times higher than that in plants treated with NO/sub 3//sup -/(NO/sub 3/-plants), and most /sup 14/C-urea exogenously supplied to detached roots of Arg-plants was immediately decomposed to /sup 14/CO/sub 2/. The urea released from arginine by arginase was cleaved to /sup 15/NH/sub 4//sup +/ + /sup 14/CO/sub 2/ by urease. Most of the /sup 14/CO/sub 2/ was then lost from the root system. On the other hand, the released /sup 15/NH/sub 4//sup +/ was reassimilated into amino acids probably through the pathway of ammonia assimilation. Released (5-/sup 3/H) ornithine was metabolized dominantly to proline.

Impacts of Stable Element Intake on C and I Dose Estimates - Implications for Proposed Yucca Mountain Repository

Energy Technology Data Exchange (ETDEWEB)

D.W. Moeller; M.T. Ryan; Lin-Shen C. Sun; R.N. Cherry Jr.

2004-12-21

The purpose of this study was to evaluate the influence of the intake of stable isotopes of carbon and iodine on the committed doses due to the ingestion of {sup 14}C and {sup 129}I. This was accomplished through the application of two different computational approaches. The first was based on the assumption that ground (drinking) water was the only source of intake of both {sup 14}C and {sup 129}I and stable carbon and stable iodine. For purposes of the second approach, the intake of {sup 14}C and {sup 129}I was still assumed to be only that in the ground (drinking) water, but the intake of stable carbon and stable iodine was assumed to be that in the drinking water plus other components of the diet. The doses were estimated using either a conversion formula or the applicable dose coefficients in Federal Guidance Reports No. 11 and No. 13. Serving as input for the analyses was the estimated maximum concentration of {sup 14}C or {sup 129}I that would be present in the ground water due to potential releases from the proposed Yucca Mountain high-level radioactive waste repository during the first 10,000 years after closure. The estimated concentrations of stable carbon and iodine were based on analyses of ground water samples collected in the Amargosa Valley, NV. Based on the accompanying analyses, three conclusions were reached. First, no dose estimate, using a conversion formula in which the ratios of the stable to radioactive isotopes of an element serve as input, should ever be made without including the stable element intake contributions from all components of the diet. Second, the study suggests that the dose coefficients for {sup 129}I in Federal Guidance Reports No. 11 and No. 12 which, in turn, are based on publications of the ICRP, may not be appropriate for application in developed nations of the world, especially those in which relatively large amounts of seafood are consumed and the use of iodized salt is common. The estimated average daily intake of

Rhodium(I)-catalyzed cycloisomerization of benzylallene-alkynes through C-H activation.

Science.gov (United States)

Kawaguchi, Yasuaki; Yasuda, Shigeo; Kaneko, Akira; Oura, Yuki; Mukai, Chisato

2014-07-14

The efficient Rh(I)-catalyzed cycloisomerization of benzylallene-alkynes produced the tricyclo[9.4.0.0(3,8)]pentadecapentaene skeleton through a C(sp2)-H bond activation in good yields. A plausible reaction mechanism proceeds via oxidative addition of the acetylenic C-H bond to Rh(I), an ene-type cyclization to the vinylidenecarbene-Rh(I) intermediate, and an electrophilic aromatic substitution with the vinylidenecarbene species. It was proposed based on deuteration and competition experiments. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

An approach for measuring the {sup 129}I/{sup 127}I ratio in fish samples

Energy Technology Data Exchange (ETDEWEB)

Kusuno, Haruka, E-mail: kusuno@um.u-tokyo.ac.jp [The University Museum, The University of Tokyo, 3-7-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Matsuzaki, Hiroyuki [The University Museum, The University of Tokyo, 3-7-1 Hongo, Bunkyo-ku, Tokyo 113-0033 (Japan); Nagata, Toshi; Miyairi, Yosuke; Yokoyama, Yusuke [Atmosphere and Ocean Research Institute, The University of Tokyo, 5-1-5, Kashiwanoha, Kashiwa-shi, Chiba 277-8564 (Japan); Ohkouchi, Naohiko [Japan Agency for Marine-Earth Science and Technology, 2-15, Natsushima-cho, Yokosuka-city, Kanagawa 237-0061 (Japan)

2015-10-15

The {sup 129}I/{sup 127}I ratio in marine fish samples was measured employing accelerator mass spectrometry. The measurement was successful because of the low experimental background of {sup 129}I. Pyrohydrolysis was applied to extract iodine from fish samples. The experimental background of pyrohydrolysis was checked carefully and evaluated as 10{sup 4}–10{sup 5} atoms {sup 129}I/combustion. The methodology employed in the present study thus required only 0.05–0.2 g of dried fish samples. The methodology was then applied to obtain the {sup 129}I/{sup 127}I ratio of marine fish samples collected from the Western Pacific Ocean as (0.63–1.2) × 10{sup −10}. These values were similar to the ratio for the surface seawater collected at the same station, 0.4 × 10{sup −10}. The {sup 129}I/{sup 127}I ratio of IAEA-414, which was a mix of fish from the Irish Sea and the North Sea, was also measured and determined as 1.82 × 10{sup −7}. Consequently, fish from the Western Pacific Ocean and the North Sea were distinguished by their {sup 129}I/{sup 127}I ratios. The {sup 129}I/{sup 127}I ratio is thus a direct indicator of the area of habitat of fish.

The synthesis of 1,2,7,11b-Tetrahydroisoxazolo[2,3-d][1,4]benzodiazepin-6(5H)-ones and 1,3,3a,9b-tetrahydroisoxazolo[4,3-c]quinolin-4(5H)-ones

OpenAIRE

Heaney, Frances; Bourke, Sharon

1995-01-01

The reaction of various ethyl 3-[[2-(1-hydroxyiminoalkyl)phenyl]carbamoyl]acrylates (2) with electron deficient olefins proceeds via a sequential dipole formation, dipolar cycloaddition sequence to furnish the tetrahydroisoxazolo[2,3-d][1,4]benzodiazepin-6(5H)-ones and tetrahydroisoxazolo[4,3-c]quinolin-4(5H)-ones (4) and (6). The product distribution reflects the nature of the reacting olefin and the position and extent of substitution on the acrylate moiety.

Determining criteria for the disposal of iodine-129

International Nuclear Information System (INIS)

Burger, L.L.

1980-10-01

The basic consideration in the disposal of the 129 I produced by the nuclear power industry is that humans must be protected from unacceptable radiation risks. Existing standards prescribe maximum concentrations in air and water and, more recently, a maximum release per unit of electrical power production. The global quantity, distribution, and rate of movement of 127 I (natural iodine), naturally produced 129 I, and anthropogenic 129 I are examined. The 129 I released earlier as a result of nuclear activities over the past few decades is not uniformly dispersed. But the possibility of much greater dispersion exists and, therefore, of much greater dilution than was previously attempted. The potential for dilution with respect to either the 129 I concentration or the 129 I/ 127 I ratio far exceeds the minimum required for acceptable exposure to mankind. For utilizing the dilution principle, it is preferable to package and dispose of 129 I separately from other fission products. The deep ocean is seen to be the logical location for ultimate disposal. A set of 14 basic items is described that can be used to set criteria for storage and disposal of 129 I. It is suggested that preliminary standards be developed on these and perhaps other items to apply to (1) temporary storage and transportation, (2) disposal to a dry environment with a time limitation on calculated behavior, and (3) disposal to the deep ocean with complete release permitted in 10 3 yr. Early quantification of some of these items will permit better decisions on further research and development needed for iodine removal or control, fixation, and disposal

Distribution of {sup 129}I in terrestrial surface water environments

Energy Technology Data Exchange (ETDEWEB)

Chen, Xuegao [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Gong, Meng [College of Hydrology and Water Resources, Hohai University, Nanjing (China); Yi, Peng, E-mail: pengyi1915@163.com [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Aldahan, Ala [Department of Earth Sciences, Uppsala University, Uppsala (Sweden); Department of Geology, United Arab Emirates University, Al Ain (United Arab Emirates); Yu, Zhongbo [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China); Possnert, Göran [Tandem Laboratory, Uppsala University, Uppsala (Sweden); Chen, Li [State Key Laboratory of Hydrology-Water Resources and Hydraulic Engineering, Hohai University, Nanjing 210098 (China); College of Hydrology and Water Resources, Hohai University, Nanjing (China)

2015-10-15

The global distribution of the radioactive isotope iodine-129 in surface waters (lakes and rivers) is presented here and compared with the atmospheric deposition and distribution in surface marine waters. The results indicate relatively high concentrations in surface water systems in close vicinity of the anthropogenic release sources as well as in parts of Western Europe, North America and Central Asia. {sup 129}I level is generally higher in the terrestrial surface water of the Northern hemisphere compared to the southern hemisphere. The highest values of {sup 129}I appear around 50°N and 40°S in the northern and southern hemisphere, separately. Direct gaseous and marine atmospheric emissions are the most likely avenues for the transport of {sup 129}I from the sources to the terrestrial surface waters. To apply iodine-129 as process tracer in terrestrial surface water environment, more data are needed on {sup 129}I distribution patterns both locally and globally.

A summary of global 129I in marine waters

International Nuclear Information System (INIS)

He Peng; Aldahan, A.; Possnert, G.; Hou, X.L.

2013-01-01

Despite the many investigations concerning the occurrence of anthropogenic iodine-129 in the atmosphere, terrestrial and marine environments, there is a lack of a comprehensive collection of data on the distribution of the isotope in marine waters. The temporal and spatial variability of anthropogenic 129 I is strongly linked to the major point sources in the Irish Sea and the English Channel and the global marine spreading pathways are partly outlined from these sources. The temporal evolution is still, however, not well defined when transport and dissipation are considered in the different oceans and ocean compartments. We here summarize available published literature data on 129 I temporal and spatial distribution in the global marine water. The results show presence of numerous data sets for the North Atlantic and Arctic Oceans where strong variability in terms of water depth, time and location also occur. Scarcity of data on 129 I from the Pacific, Indian and South Atlantic Oceans demonstrates gaps in the coverage of the isotope spatial extent. These shortcomings in the spatial coverage may relate to the understanding that the anthropogenic 129 I signal will take a long time to be transported, if at all, from the North Atlantic into other oceans. Data from recent expeditions in the Southern oceans and the Geotraces ocean profiling will reveal additional information about 129 I distribution in the marine waters.

Gold(I) Complexes with N-Donor Ligands. 2.(1) Reactions of Ammonium Salts with [Au(acac-kappaC(2))(PR(3))] To Give [Au(NH(3))L](+), [(AuL)(2)(&mgr;(2)-NH(2))](+), [(AuL)(4)(&mgr;(4)-N)](+), or [(AuL)(3)(&mgr;(3)-O)](+). A New and Facile Synthesis of [Au(NH(3))(2)](+) Salts. Crystal Structure of [{AuP(C(6)H(4)OMe-4)(3)}(3)(&mgr;(3)-O)]CF(3)SO(3).

Science.gov (United States)

Vicente, José; Chicote, María-Teresa; Guerrero, Rita; Jones, Peter G.; Ramírez De Arellano, M. Carmen

1997-09-24

The complexes [Au(acac-kappaC(2))(PR(3))] (acac = acetylacetonate, R = Ph, C(6)H(4)OMe-4) react with (NH(4))ClO(4) to give amminegold(I), [Au(NH(3))(PR(3))]ClO(4), amidogold(I), [(AuPR(3))(2)(&mgr;(2)-NH(2))]ClO(4), or nitridogold(I), [(AuPR(3))(4)(&mgr;(4)-N)]ClO(4), complexes, depending on the reaction conditions. Similarly, [Au(acac-kappaC(2))(PPh(3))] reacts with (NH(3)R')OTf (OTf = CF(3)SO(3)) (1:1) or with [H(3)N(CH(2))(2)NH(2)]OTf (1:1) to give (amine)gold(I) complexes [Au(NH(2)R')(PPh(3))]OTf (R' = Me, C(6)H(4)NO(2)-4) or [(AuPPh(3))(2){&mgr;(2)-H(2)N(CH(2))(2)NH(2)}](OTf)(2), respectively. The ammonium salts (NH(2)R'(2))OTf (R' = Et, Ph) react with [Au(acac-kappaC(2))(PR(3))] (R = Ph, C(6)H(4)OMe-4) (1:2) to give, after hydrolysis, the oxonium salts [(AuPR(3))(3)(&mgr;(3)-O)]OTf (R = Ph, C(6)H(4)OMe-4). When NH(3) is bubbled through a solution of [AuCl(tht)] (tht = tetrahydrothiophene), the complex [Au(NH(3))(2)]Cl precipitates. Addition of [Au(NH(3))(2)]Cl to a solution of AgClO(4) or TlOTf leads to the isolation of [Au(NH(3))(2)]ClO(4) or [Au(NH(3))(2)]OTf, respectively. The crystal structure of [(AuPR(3))(3)(&mgr;(3)-O)]OTf.Me(2)CO (R = C(6)H(4)OMe-4) has been determined: triclinic, space group P&onemacr;, a = 14.884(3) Å, b = 15.828(3) Å, c = 16.061(3) Å, alpha = 83.39(3) degrees, beta = 86.28(3) degrees, gamma = 65.54(3) degrees, R1 (wR2) = 0.0370 (0.0788). The [(AuPR(3))(3)(&mgr;(3)-O)](+) cation shows an essentially trigonal pyramidal array of three gold atoms and one oxygen atom with O-Au-P bond angles of ca. 175 degrees and Au.Au contacts in the range 2.9585(7)-3.0505(14) Å. These cations are linked into centrosymmetric dimers through two short Au.Au [2.9585(7), 3.0919(9) Å] contacts. The gold atoms of the dimer form a six-membered ring with a chair conformation.

A 60-year record of 129I in Taal Lake sediments (Philippines): Influence of human nuclear activities at low latitude regions.

Science.gov (United States)

Zhang, Luyuan; Hou, Xiaolin; Li, Hong-Chun; Xu, Xiaomei

2018-02-01

The influence of human nuclear activities on environmental radioactivity is not well known at low latitude regions that are distant from nuclear test sites and nuclear facilities. A sediment core collected from Taal Lake in the central Philippines was analyzed for 129 I and 127 I to investigate this influence in a low-latitude terrestrial system. A baseline of 129 I/ 127 I atomic ratios was established at (2.04-5.14) × 10 -12 in the pre-nuclear era in this region. Controlled by the northeasterly equatorial trade winds, increased 129 I/ 127 I ratios of (20.1-69.3) × 10 -12 suggest that atmospheric nuclear weapons tests at the Pacific Proving Grounds in the central Pacific Ocean was the major source of 129 I in the sediment during 1956-1962. The 129 I/ 127 I ratios, up to 157.5 × 10 -12 after 1964, indicate a strong influence by European nuclear fuel reprocessing plants. The East Asian Winter Monsoon is found to be the dominant driving force in the atmospheric dispersion of radioactive iodine ( 129 I) from the European nuclear fuel reprocessing plants to Southeast Asia, which is also important for dispersion of other airborne pollutants from the middle-high to low latitude regions. A significant 129 I/ 127 I peak at 42.8 cm in the Taal Lake core appears to be the signal of the Chernobyl accident in 1986. In addition, volcanic activities are reflected in the iodine isotope profiles in the sediment core, suggesting the potential of using iodine isotopes as an indicator of volcanic eruptions. Copyright © 2017 Elsevier Ltd. All rights reserved.

Mononuclear Amido and Binuclear Imido Zirconium Complexes Supported by Dibenzotetraaza[14]annulene Ligands. X-ray Structure of [(Me(4)taa)Zr(&mgr;-NR)(2)Zr(NHR)(2)] (R = Bu(t) or 2,6-C(6)H(3)Me(2)).

Science.gov (United States)

Nikonov, Georgii I.; Blake, Alexander J.; Mountford, Philip

1997-03-12

Reaction of 2 equiv of Li[NH-2,6-C(6)H(3)R(2)] with [(Me(4)taa)ZrCl(2)] (Me(4)taaH(2) = tetramethyldibenzotetraaza[14]annulene) gives the bis(amido) derivatives [(Me(4)taa)Zr(NH-2,6-C(6)H(3)R(2))(2)] [R = Pr(i) (1) and Me (2)]. Addition of Me(4)taaH(2) to [Zr(N-2,6-C(6)H(3)Pr(i)(2))(NH-2,6-C(6)H(3)Pr(i)(2))(2)(py)(2)] also affords 1. The reaction of 2 equiv of aryl or alkyl amines H(2)NR with the bis(alkyl) complex [(Me(4)taa)Zr(CH(2)SiMe(3))(2)] is the most versatile method for preparing [(Me(4)taa)Zr(NHR)(2)] (R = 2,6-C(6)H(3)Pr(i)(2), 2,6-C(6)H(3)Me(2), Ph, or Bu(t)). Reaction of 1 equiv of Me(4)taaH(2) with the binuclear complexes [(Bu(t)NH)(2)Zr(&mgr;-NBu(t))(2)Zr(NHBu(t))(2)] or [(py)(HN-2,6-C(6)H(3)Me(2))(2)Zr(&mgr;-N-2,6-C(6)H(3)Me(2))(2)Zr(NH-2,6-C(6)H(3)Me(2))(2)(py)] gives the asymmetrically substituted derivatives [(Me(4)taa)Zr(&mgr;-NR)(2)Zr(NHR)(2)] [R = Bu(t) (6) or 2,6-C(6)H(3)Me(2) (8)], which have been crystallographically characterized.

Lethal Effect on Bacterium of Decay of Incorporated Radioactive Atoms (3H, 14C, 32P)

International Nuclear Information System (INIS)

Apelgot, Sonia

1968-01-01

The biological effect of decay of 3 H, 14 C and 32 P incorporated into a bacterium depends on the nature of the organic molecule labelled, on the position of the isotope within it and on the isotope itself. In sum, results obtained to date show that: The decay of 3 H atoms incorporated into certain macromolecules of a bacterium causes sterilization through ionization by the ß - particle emitted; transmutation is of negligible importance. This self-irradiation is comparable in effect with X-rays and is affected in a similar manner by the same factors: temperature, presence of a radioprotector, radiosensitivity of the strain. Decay of 14 C or 32 P atoms incorporated into bacterial DNA is lethal because of the transmutation effect; ionizations produced by emitted ß - particles may be disregarded. Survival curves for 32 P transmutations depend on the experimental conditions. Some of the results obtained with 32 P are similar to those obtained with X-rays, e.g. effects of temperature, radical capture and oxygen, while others are similar to those of u.v. light, e.g., effect of growth conditions. Comparative tests made with 32 P indicate that the recoil energy of transmutation is not the phenomenon responsible for the lethal effect observed. Comparison of the results obtained after X-irradiation or decay of 3 H or 32 P incorporated into the DNA of bacteria of the same strain of E. coli shows that the efficiency of a 32 P transmutation is about four times greater than that of an ionization produced at random within the same DNA. (author) [fr

Chemical Speciation Analysis and Environmental Behaviour of ¹²⁷I and ¹²⁹I

DEFF Research Database (Denmark)

Hansen, Violeta

2011-01-01

may be a slow process while along the Baltic Sea surface water reduction of iodate is a relatively fast process. Although suboxic or anoxic condition are encountered in some of the Baltic Sea deep basins, the concentration of 129IO3 - increases with water depth indicating that the reduction of iodate......) in environmental samples are very complex and strongly dependent on several factors, such as water/soil/sediment chemistry, seaweed type, different pH, Eh, quantity and quality of organic matter, microbiological activity as well as differences in contaminant origin. The 129I isotope, where the main inventory has...... in the oxygen deficient bottom water of the Baltic Sea is a slow process. Iodine chemical speciation analysis (as iodide, iodate and total iodine including inorganic and organic iodine species) in lake water samples collected from Denmark and southern Sweden has been carried out. Destruction of organic iodine...

Microdosimetry of 129I in the human thyroid

International Nuclear Information System (INIS)

Feige, Y.

1977-01-01

A microdosimetric evaluation of the dose distribution from I-129 in the human thyroid gland, taking into account the various physical, geometrical and physiological parameters suggested by the ICRP Pub. 23 (1975) will be presented, and compared to the dose distribution of other radioisotopes of iodine. Using Dillman's decay scheme data, (NM/MIRD No. 10, p. 73, 1975), and the methods applied by Feige et al. for the microdosimetry of I-125, it is found that the dose to the cell nucleus is about 60% of the 'average' calculated dose for the whole thyroid gland. This follows from the assumptions that typical thyroid follicles are 150 to 300μm in diameter, and that all the iodine is contained in the colloid fraction of the gland. Thus a significant part of the decay energy of I-129, which is due mainly to the beta particles whose average range in tissue is only about 30 μm, is deposited within the colloid itself, and fails to reach the cell nucleus, 3 μm away from the colloid/cell interface. Uncertainties and variations in the parameters of the thyroid model will also be discussed. When thyroid doses due to I-129 releases are assessed, by either the specific activity or the critical pathway models, the conservative environmental and biological assumptions usually made lead to a large margin of safety. If 'average' doses are used instead of the microdosimetric dose distribution an additional safety factor of about 2 is obtained

Potential antimicrobial agents from triazole-functionalized 2H-benzo[b][1,4]oxazin-3(4H)-ones.

Science.gov (United States)

Bollu, Rajitha; Banu, Saleha; Bantu, Rajashaker; Reddy, A Gopi; Nagarapu, Lingaiah; Sirisha, K; Kumar, C Ganesh; Gunda, Shravan Kumar; Shaik, Kamal

2017-12-01

A series of substituted triazole functionalized 2H-benzo[b][1,4]oxazin-3(4H)-ones were synthesized by employing click chemistry and further characterized based on 1 H NMR, 13 C NMR, IR and mass spectral studies. All the synthesized derivatives were screened for their in vitro antimicrobial activities. Further, molecular docking studies were accomplished to explore the binding interactions between 1,2,3-triazol-4-yl-2H-benzo[b][1,4]oxazin-3(4H)-one and the active site of Staphylococcus aureus (CrtM) dehydrosqualene synthase (PDB ID: 2ZCS). These docking studies revealed that the synthesized derivatives showed high binding energies and strong H-bond interactions with the dehydrosqualene synthase validating the observed antimicrobial activity data. Based on antimicrobial activity and docking studies, the compounds 9c, 9d and 9e were identified as promising antimicrobial leads. Copyright © 2017 Elsevier Ltd. All rights reserved.

Three closely related 4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridines: synthesis, molecular conformations and hydrogen bonding in zero, one and two dimensions.

Science.gov (United States)

Sagar, Belakavadi K; Harsha, Kachigere B; Yathirajan, Hemmige S; Rangappa, Kanchugarakoppal S; Rathore, Ravindranath S; Glidewell, Christopher

2017-03-01

In each of 1-(4-fluorophenyl)-5-methylsulfonyl-3-[4-(trifluoromethyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine, C 21 H 19 F 4 N 3 O 2 S, (I), 1-(4-chlorophenyl)-5-methylsulfonyl-3-[4-(trifluoromethyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine, C 21 H 19 ClF 3 N 3 O 2 S, (II), and 1-(3-methylphenyl)-5-methylsulfonyl-3-[4-(trifluoromethyl)phenyl]-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridine, C 22 H 22 F 3 N 3 O 2 S, (III), the reduced pyridine ring adopts a half-chair conformation with the methylsulfonyl substituent occupying an equatorial site. Although compounds (I) and (II) are not isostructural, having the space groups Pbca and P2 1 2 1 2 1 , respectively, their molecular conformations are very similar, but the conformation of compound (III) differs from those of (I) and (II) in the relative orientation of the N-benzyl and methylsulfonyl substituents. In compounds (II) and (III), but not in (I), the trifluoromethyl groups are disordered over two sets of atomic sites. Molecules of (I) are linked into centrosymmetric dimers by C-H...π(arene) hydrogen bonds, molecules of (II) are linked by two C-H...O hydrogen bonds to form ribbons of R 3 3 (18) rings, which are themselves further linked by a C-Cl...π(arene) interaction, and a combination of C-H...O and C-H...π(arene) hydrogen bonds links the molecules of (III) into sheets. Comparisons are made with the structures of some related compounds.

Measurements and analysis of the 127I and 129I neutron capture and total cross sections

International Nuclear Information System (INIS)

Noguere, G.

2005-01-01

Most of the experimental work on the interaction of neutrons with matter has focused on materials important to reactor physics and reactor structures. By comparison, the corresponding data for minor actinides or long-lived fission products are poor. A significant demand has developed for improved neutron cross-section data of these little-studied nuclides due to the surge of interest in the transmutation of nuclear waste. With 400 kg of 129 I produced yearly in the reactors of the EU countries and a very long β - half-life of 1.57 x 10 7 years, iodine requires disposal strategies that will isolate this isotope from the environment for long periods of time. Therefore, 129 I is potentially a key long-lived fission product for transmutation applications, since 129 I transmutes in 130 I after a single neutron capture and decays to 130 Xe with a 12.36 h half-life. Accurate capture cross sections would help to reduce uncertainties in waste management concepts. For that purpose, Time-Of-Flight measurements covering the [0.5 eV-100 keV] energy range have been carried out at the 150 MeV pulsed neutron source GELINA of the Institute for Reference Materials and Measurements (IRMM). Two types of experiments have been performed at the IRMM, namely capture and transmission experiments. They are respectively related to the neutron capture and total cross sections. Since the PbI 2 samples used in this work contain natural and radioactive iodine, extensive measurements of 129 I have been carried out under the same experimental conditions as for the 129 I. The data reduction process was performed with the AGS system, and the resonance parameters were extracted with the SAMMY and REFIT shape analysis codes. In a last step, the parameters have been converted into ENDF-6 format and processed with the NJOY code to produce point-wise and multigroup cross sections, as well as MCNP and ERANOS libraries. (author)

Low-level liquid scitillation counting for quantification of annual {sup 3}H and {sup 14}C concentrations in tree disks

Energy Technology Data Exchange (ETDEWEB)

Kopka, B [Goettingen Univ. (Germany). Isotopenlaboratorium fuer Biologische und Medizinische Forschung; Schikowski, J [Goettingen Univ. (Germany). Isotopenlaboratorium fuer Biologische und Medizinische Forschung; Porstendoerfer, J [Goettingen Univ. (Germany). Isotopenlaboratorium fuer Biologische und Medizinische Forschung

1997-03-01

The government of Schleswig Holstein funded a study to perform the retrospective determination of airborne {sup 3}H and {sup 14}C concentrations. It is well known, that in tree rings most of the hydrogen and cabron is fixed after insertion in the matrix of wood and that the radionuclide concentration correlates with former airborne activity concentrations. For the retrospective study wood disks of trees located in the region near the nuclear power plant of Kruemmel and control disks of unsuspected areas were selected. The hydrogen of the wood was transformed to water and the carbon to carbondioxide by classical oxidation processes (combustion in a furnace). The contents of {sup 3}H in the water and {sup 14}C of the carbondioxide (solved in scintillation liquid) were determined by liquid scintillation counting, using a low-level counter (type Quantulus 1220, Wallac). (orig.)

Reactions of 11C recoil atoms in the systems H2O-NH3, H2O-CH4 and NH3-CH4

International Nuclear Information System (INIS)

Nebeling, B.

1988-11-01

In this study the chemical reactions of recoil carbon 11 in the binary gas mixtures H 2 O-NH 3 , H 2 O-CH 4 and NH 3 -CH 4 in different mixing ratios as well as in solid H 2 O and in a solid H 2 O-NH 3 mixture were analyzed in dependence of the dose. The analyses were to serve e.g. the simulation of chemical processes caused by solar wind, solar radiation and cosmic radiation in the coma and core of comets. They were to give further information about the role of the most important biogeneous element carbon, i.e. carbon, in the chemical evolution of the solar system. Besides the actual high energy processes resulting in the so-called primary products, also the radiation-chemical changes of the primary products were also observed in a wide range of dosing. The generation of the energetic 11 C atoms took place according to the target composition by the nuclear reactions 14 N(p,α) 11 C, 12 C( 3 He,α) 11 C or the 16 O(p,αpn) 11 C reaction. The identification of the products marked with 11 C was carried out by means of radio gas chromatography or radio liquid chromatography (HPLC). (orig./RB) [de

C-H and H-H Bond Activation via Ligand Dearomatization/Rearomatization of a PN3P-Rhodium(I) Complex

KAUST Repository

Huang, Kuo-Wei

2015-04-13

A neutral complex PN3P-Rh(I)Cl (2) was prepared from a reaction of the PN3P pincer ligand (1) with [Rh(COD)Cl]2 (COD = 1,5-cyclooctadiene). Upon treatment with a suitable base, H–H and Csp2–H activation reactions can be achieved through the deprotonation/reprotonation of one of the N–H arms and dearomatization/rearomatization of the central pyridine ring with the oxidation state of Rh remaining I.

High-resolution 129I bomb peak profile in an ice core from SE-Dome site, Greenland.

Science.gov (United States)

Bautista, Angel T; Miyake, Yasuto; Matsuzaki, Hiroyuki; Iizuka, Yoshinori; Horiuchi, Kazuho

2018-04-01

129 I in natural archives, such as ice cores, can be used as a proxy for human nuclear activities, age marker, and environmental tracer. Currently, there is only one published record of 129 I in ice core (i.e., from Fiescherhorn Glacier, Swiss Alps) and its limited time resolution (1-2 years) prevents the full use of 129 I for the mentioned applications. Here we show 129 I concentrations in an ice core from SE-Dome, Greenland, covering years 1956-1976 at a time resolution of ∼6 months, the most detailed record to date. Results revealed 129 I bomb peaks in years 1959, 1962, and 1963, associated to tests performed by the former Soviet Union, one year prior, in its Novaya Zemlya test site. All 129 I bomb peaks were observed in winter (1958.9, 1962.1, and 1963.0), while tritium bomb peaks, another prominent radionuclide associated with nuclear bomb testing, were observed in spring or summer (1959.3, and 1963.6; Iizuka et al., 2017). These results indicate that 129 I bomb peaks can be used as annual and seasonal age markers for these years. Furthermore, we found that 129 I recorded nuclear fuel reprocessing signals and that these can be potentially used to correct timing of estimated 129 I releases during years 1964-1976. Comparisons with other published records of 129 I in natural archives showed that 129 I can be used as common age marker and tracer for different types of records. Most notably, the 1963 129 I bomb peak can be used as common age marker for ice and coral cores, providing the means to reconcile age models and associated trends from the polar and tropical regions, respectively. Copyright © 2017 Elsevier Ltd. All rights reserved.

The synthesis of 5'-[14C1] and 3a, 4-[13C2] labelled panadiplon (U-78875; 3-(5'-cyclopropyl-1,2,4-oxadiazol-3-yl)-5-(1-methylethyl)-imidazo-[1,5a]-quinoxalin-4(5H)-one)

International Nuclear Information System (INIS)

Ackland, M.J.; Howard, M.R.; Dring, L.G.

1993-01-01

5'-[ 14 C 1 ]Panadiplon was prepared in 3 steps starting from [ 14 C 1 ]cyclopropane carboxylic acid and 3-(5'-cyano-1,2,4-oxadiazol-3-yl)-5-(1-methylethyl)-imidazo-[1,5a] -quinoxalin-4(5H)-one. 3a, 4-[ 13 C 2 ]Panadiplon was prepared in two steps from 13 C 2 -oxalic acid and N-1-(1-methylethyl)-o-phenylenediamine. The position of labelling was confirmed by the appearance of two coupled resonances (J C-C =80.59 Hz) at 121.95 and 154.39 ppm in the assigned 13 C-NMR spectrum. (Author)

Synthesis of [triazole-3(5)-14C]-propiconazole stereoisomers

International Nuclear Information System (INIS)

Hadjidemetriou, D.; Loeffler, R.T.

1992-01-01

A preparation of all four stereoisomers of the fungicide and sterol biosynthesis inhibitor propiconazole (1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole), labelled with [ 14 C] in the triazole ring, is described. (author)

Semiconducting perovskites (2-XC6H4C2H4NH3)2SnI4 (X = F, Cl, Br): steric interaction between the organic and inorganic layers.

Science.gov (United States)

Xu, Zhengtao; Mitzi, David B; Dimitrakopoulos, Christos D; Maxcy, Karen R

2003-03-24

Two new semiconducting hybrid perovskites based on 2-substituted phenethylammonium cations, (2-XC(6)H(4)C(2)H(4)NH(3))(2)SnI(4) (X = Br, Cl), are characterized and compared with the previously reported X = F compound, with a focus on the steric interaction between the organic and inorganic components. The crystal structure of (2-ClC(6)H(4)C(2)H(4)NH(3))(2)SnI(4) is solved in a disordered subcell [C2/m, a = 33.781(7) A, b = 6.178(1) A, c = 6.190(1) A, beta = 90.42(3)(o), and Z = 2]. The structure is similar to the known (2-FC(6)H(4)C(2)H(4)NH(3))(2)SnI(4) structure with regard to both the conformation of the organic cations and the bonding features of the inorganic sheet. The (2-BrC(6)H(4)C(2)H(4)NH(3))(2)SnI(4) system adopts a fully ordered monoclinic cell [P2(1)/c, a = 18.540(2) A, b = 8.3443(7) A, c = 8.7795(7) A, beta = 93.039(1)(o), and Z = 2]. The organic cation adopts the anti conformation, instead of the gauche conformation observed in the X = F and Cl compounds, apparently because of the need to accommodate the additional volume of the bromo group. The steric effect of the bromo group also impacts the perovskite sheet, causing notable distortions, such as a compressed Sn-I-Sn bond angle (148.7(o), as compared with the average values of 153.3 and 154.8(o) for the fluoro and chloro compounds, respectively). The optical absorption features a substantial blue shift (lowest exciton peak: 557 nm, 2.23 eV) relative to the spectra of the fluoro and chloro compounds (588 and 586 nm, respectively). Also presented are transport properties for thin-film field-effect transistors (TFTs) based on spin-coated films of the two hybrid semiconductors.

Measurements and hydrological applications of 3H and 14C

International Nuclear Information System (INIS)

Rauert, W.

1980-08-01

A survey is given on the occurence of T and C 14 in the environment and pertinent low-level measuring techniques. T is used as artificial tracer for flow studies in laboratory and field tests. Examples are presented for the use of environmental T and C 14 to investigate shallow and deep groundwater and brines, and their interrelation with precipitation and surface water. Problems of sampling of deep groundwater are dealt with. (orig.) [de

Proton relays in anomalous carbocations dictate spectroscopy, stability, and mechanisms: case studies on C2H5+ and C3H3.

Science.gov (United States)

Sager, LeeAnn M; Iyengar, Srinivasan S

2017-10-18

We present a detailed analysis of the anomalous carbocations: C 2 H 5 + and C 3 H 3 + . This work involves (a) probing electronic structural properties, (b) ab initio dynamics simulations over a range of internal energies, (c) analysis of reduced dimensional potential surfaces directed along selected conformational transition pathways, (d) dynamically averaged vibrational spectra computed from ab initio dynamics trajectories, and (e) two-dimensional time-frequency analysis to probe conformational dynamics. Key findings are as follows: (i) as noted in our previous study on C 2 H 3 + , it appears that these non-classical carbocations are stabilized by delocalized nuclear frameworks and "proton shuttles". We analyze this nuclear delocalization and find critical parallels between conformational changes in C 2 H 3 + , C 2 H 5 + , and C 3 H 3 + . (ii) The vibrational signatures of C 2 H 5 + are dominated by the "bridge-proton" conformation, but also show critical contributions from the "classical" configuration, which is a transition state at almost all levels of theory. This result is further substantiated through two-dimensional time-frequency analysis and is at odds with earlier explanations of the experimental spectra, where frequencies close to the classical region were thought to arise from an impurity. While this is still possible, our results here indicate an additional (perhaps more likely) explanation that involves the "classical" isomer. (iii) Finally, in the case of C 3 H 3 + our explanation of the experimental result includes the presence of multiple, namely, "cyclic", "straight", and propargyl, configurations. Proton shuttles and nuclear delocalization, reminiscent of those seen in the case of C 2 H 3 + , were seen all through and have a critical role in all our observations.

129I in the environment around a nuclear reprocessing plant

International Nuclear Information System (INIS)

Joshi, S.N.; Doshi, G.R.

1988-01-01

129 I and 131 I activities are measured in leaf samples collected within Trombay region, covering a radius of 4500 m from the reprocessing plant. The concentration of 129 I and 131 I in dried leaf samples ranged from 0.04 to 1.28 pCi/gm and 4 to 5 pCi/gm respectively. A radiochemical procedure involving distillation and solvent extractions of 129 I and then counting in a Liquid Scintillation Spectrometer is used for its final determination. The concentration of 129 I observed in leaf samples collected at the south site gate is used to calculate the dose commitment to an adult via grass-cow-milk pathway. On the basis of conservative assumption that the activity present in the grass would be equal to that in the leaf, the dose commitment to an adult through milk ingestion route will not exceed 5.5 μSv/y. (author). 2 tabs., 13 refs

Iodine-129 in the environment

International Nuclear Information System (INIS)

Tikhomirov, F.A.; Moiseev, I.T.

1987-01-01

The quantitative ratio of aerial and soil entries of 129 I into plants, parameters of its migration in the system of atmosphere-soil-plants-river water, dynamics of transformation and biological availability of 129 I in soil for plants were studied on the basis of field observations and experiments using the radioactive tracers. The doses of human thyroid gland irradiation by 129 I under atmospheric and soil pathways of its transport into diet are estimated. 129 I content in soil due to its systematic, for 50 years, releases into atmosphere is shown to be negligible, agricultural production contamination by 129 I resulting mainly from its fallout onto overground phytomass. The period, needed to achieve 129 I concentration equilibrium in the atmosphere-soil system under constant average 129 I content in the air, varies depending on the soil type from several hundred years (for podzolic soils) up to several thousand years (for chernozem). The 129 I half-accumulation period is equal to 150 years for soddy-podzolic soil and to 700 years for chernozem. In case of 129 I fallout lasting for 100 years the annual increase of its content in overground phytomass due to the transport from soil will account for 0,3% of its atmospheric entry way for soddy-podzolic soil and for 0,1% for chernozem, respectively. For a number of sierozem, yellow soil and calcareous chernozem types this addition is higher (up to 1%). Under constant iodine-129 concentration in air (1 Bq/m3) the absorbed dose for one-year child's thyroid gland in continental area is approximately equal to 2 (Gy/y)/(Bq/m3). The absorbed dose from globally dissipated 129 I under 99% efficiency of gas purification will not exceed 2·10 -7 Gy/y. The input of globally dissipated 129 I, originating from deep underground disposal of nuclear wastes can account for not more than 10 -9 Gy/y. In total, 129 I releases for the coming century is not going to produce limitations for nuclear energetics development. (author)

Lethal Effect on Bacterium of Decay of Incorporated Radioactive Atoms ({sup 3}H, {sup 14}C, {sup 32}P); Effet Letal de la Desintegration d'Atomes Radioactifs ({sup 3}H, {sup 14}C, {sup 32}P) Incorpores dans une Bacterie

Energy Technology Data Exchange (ETDEWEB)

Apelgot, Sonia [Laboratoire Curie, Institut du Radium, Paris (France)

1968-06-15

The biological effect of decay of {sup 3}H, {sup 14}C and {sup 32}P incorporated into a bacterium depends on the nature of the organic molecule labelled, on the position of the isotope within it and on the isotope itself. In sum, results obtained to date show that: The decay of {sup 3}H atoms incorporated into certain macromolecules of a bacterium causes sterilization through ionization by the ss{sup -} particle emitted; transmutation is of negligible importance. This self-irradiation is comparable in effect with X-rays and is affected in a similar manner by the same factors: temperature, presence of a radioprotector, radiosensitivity of the strain. Decay of {sup 14}C or {sup 32}P atoms incorporated into bacterial DNA is lethal because of the transmutation effect; ionizations produced by emitted ss{sup -} particles may be disregarded. Survival curves for {sup 32}P transmutations depend on the experimental conditions. Some of the results obtained with {sup 32}P are similar to those obtained with X-rays, e.g. effects of temperature, radical capture and oxygen, while others are similar to those of u.v. light, e.g., effect of growth conditions. Comparative tests made with {sup 32}P indicate that the recoil energy of transmutation is not the phenomenon responsible for the lethal effect observed. Comparison of the results obtained after X-irradiation or decay of {sup 3}H or {sup 32}P incorporated into the DNA of bacteria of the same strain of E. coli shows that the efficiency of a {sup 32}P transmutation is about four times greater than that of an ionization produced at random within the same DNA. (author) [French] L'effet biologique de la desintegration de {sup 3}H, {sup 14}C et {sup 32}P incorpores dans une bacterie depend de la nature de la molecule organique marquee, de l'emplacement de l'isotope sur celle-ci et de la nature de l'isotope lui-meme. L'ensemble des resultats obtenus a ce jour montre que la desintegration des atomes de {sup 3}H incorpores dans certaines

Synthesis of new 1H-1,2,3-triazole-1,4-naphthoquinones

Directory of Open Access Journals (Sweden)

Wagner O. Valença

2012-06-01

Full Text Available In this work, were synthesized new 1H-1,2,3-triazole-1,4-naphthoquinones via 1,3-dipolar cycloaddition reaction using CuI/acetonitrile without addition of base or ligand. The compounds (3a-i were obtained in moderate-to-good yields 45-92%. To prepare (3d, we obtain a mixture of (3d and (4 in a ratio 3:1, that it was difficult to separate. The low yield for the compound (3f can be also justified based in the formation of aminonaphthoquinone (4. The acetylation of (3h and (3i afforded the compounds (5 and (6 in 77% and 35% of yields, respectively. The low yield of (6 was due to formation of 35 % of the elimination product (7.

Designing of 14C, 3H-labeled liposomal preparations and their distribution in inner organs of experimental animals

International Nuclear Information System (INIS)

Isaev, E.I.; Kamalova, M.E.; Isakova, A.V.; Mirakhmedov, F.K.; Saatov, T.S.

2004-01-01

Full text: Development of methods for introduction of drug liposomal forms into practice is an urgent task for medicine and radiobiology. Per oral way of administration of the medications has been unexplored properly yet. Preservation of their stability in the gastro-intestinal tract is the essential requirement to the liposomes. Literature data and our studies showed that the elevated saturation of fatty acids and viscosity of liposomal membrane bilayer increases their stability to acidic and alkaline media of the digestive system. To prepare the liposome we used 14C,H-labeled lipids isolated from tissues by means of preparative chromatography after administration of D(1-614C)glucose (specific radioactivity 100 mkCu/mM) as well as of D(1-3H)-galactose (specific radioactivity 900 mkCU/mM) to 10 rats. Organ-specific liposomes were prepared in accordance with the special method without ultrasound processing to administered them with milk per orally to rats by means of a gastric probe. Before administration of 14C,3H liposomes the animals were not fed for 16-20 hours for complete emptying of the gastrointestinal tract. Under these conditions 1-1.5 hours after administration of liposomes their maximum amount was absorbed from he intestine. We found tissue specificity of the liposome administered. If the amount of administered liposomes for each tissue to be taken for 100%, in target organs their distribution (in %) would be as follows: 0.30/0.39 in the heart, 0.54/0.06 in the skeletal muscle, 0.4/0.6 in the brain, 4.2/10.2 in the spleen, 2.9/6.1 in the pancreas, 5.1/1.2 in the kidney. In these experiments liposomes had covering of 14 C, 3 H-glycosphingolipids of the spleen. Under these conditions 3H-cAMP in the form of liposomes was administered to mice per orally to measure radioactivity (in cpm 100mg of tissue) in the organs. The values were as follows: 77±6.3 in the liver, 750±47 in the spleen, 250±19 in the kidney, 70±77 in the heart, 267±21 in the lung and 95

Hydration reactions in pastes C3S+C3A+CaSO4.2aq+H20 at 25°C.I

NARCIS (Netherlands)

Corstanje, W.A.; Stein, H.N.; Stevels, J.M.

1973-01-01

A characteristic retardation of the hydration of C3A is found in pastes C3S+C3A+CaSO4.2aq+H2O of weight ratios 1:3:z:4 at certain values of z, when sulphate concentration becomes insufficient for monosulphate formation. This retardation is ascribed to precipitation of amorphous Al(OH)3, when C3A

The role of leucine in isoprenoid metabolism. Incorporation of [3-13C]leucine and of [2-3H,4-14C]-β,β-dimethyl-acrylic acid into phytosterols by tissue cultures of Andrographis paniculata

International Nuclear Information System (INIS)

Anastasis, P.; Freer, I.; Overton, K.; Rycroft, D.; Singh, S.B.

1985-01-01

[3- 13 C]Leucine is incorporated into phytosterols by tissue cultures of Andrographis paniculata by breakdown to acetyl-CoA and its subsequent incorporation via (3S)-3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) and mevalonic acid; [2- 3 H,4- 14 C]-β,β-dimethylacrylic acid also is not incorporated intact. (author)

Phyto remediation of 14C-fenvalerate insecticide contamination by fresh water weed potamogeton sp

International Nuclear Information System (INIS)

Kamel, H.A.; Aly, M.A.S.

2003-01-01

The present experiment was carried out to throw some light on the possibility of the fresh water-weed P otamogeton sp for the phyto remediation of 14 C-fenvalerate residues. In addition, the effect of the insecticide on some physiological parameters was also investigated. At the beginning of the experiment(zero time), 14 C-fenvalerate from a previous experiment carried out earlier in an aquarium in the laboratory. The potamogeton plants (125 g) having newly grown roots were transplanted in the aquarium. The amount of 14 C-activity in water was remarkably decreased from 6.54μg/ml at zero time to 1.84μg/ml at the end of the experiment (384 h). In the soil, a slight decrease in 14 C-activity was recorded from 15.23μg/g at zero time to 13.7μg/g at the end of the experiment. On the other hand, 14 C-activity in the plant was increased during the mentioned period by about 19.1%. Control and treated samples showed an increase in both chlorophyll a and b up to 96 h then their values were decreased thereafter. The carotenoid fractions in the tested plants were increased gradually up to 96 h then decreased relative to the control samples. Soluble sugars in treated plants showed maximum increase at 48 h (129.8%) then decreased to 114.3% at 192 h and to 104.7% at 384 h but still had higher values than those at zero time. A slight and gradual increase in the protein content of the treated Potamogeton plants was occurred at the first 24 h, then started to decrease than the values of corresponding controls starting from 48 h to 384 h

Methods of iodine-129 analysis for environmental monitoring

International Nuclear Information System (INIS)

Yamato, Aiji; Miyagawa, Naoto; Nomura, Tamotsu; Kinoshita, Mutsumi

1976-01-01

Some methods for the analysis of I-129 in the environment are described. Iodide ion in seawater is coprecipitated with chloride ion by silver citrate powder, and that in seaweeds and in sediment is sublimated by heating at about 900 0 C in O 2 atmosphere, and then the iodine is trapped in cooled NaOH and NaHSO 3 mixed solution. The trapped iodine is precipitated with AgNO 3 solution for γ-/X-ray spectrometry (detection limit asymptotically equals 30 pCi), or extracted into toluene scintillater solution for liquid scintillation counting. The decomposition of AgI is necessary for low level I-129 measurement; The AgI was transfered in a flask, added with 2N H 2 SO 4 and Zn sand, and decomposed by stirring for 2 hr. Filtered the solution, added 0.5 g of NaNO 2 and toluene scintillater to extract the iodine then added 1 ml of 2-methyl 1-butene to decolorize, the solution is measured by a liquid scintillation counter (detection limit asymptotically equals 1 pCi). This method can be applied for monitoring of low level radioactive water waste. (auth.)

First experiments on transmutation studies of iodine-129 and neptunium-237 using relativistic protons of 3.7 GeV

International Nuclear Information System (INIS)

Krivopustov, M.I.; Adam, J.; Bradnova, V.

1997-01-01

First experiments on the transmutation of long-lived 129 I and 237 Np using relativistic protons of 3.7 GeV are described. Relativistic protons generate in extended Pb-targets substantial neutron fluences. These neutrons get moderated in paraffin and are used for transmutation as follows: 129 (n, γ) 130 I(β - ) → 130 Xe(stable) and 237 Np(n, γ) 238 Np(β - ) →. The isotopes 130 I (T 1/2 =12.36 h) and 238 Np (T 1/2 =2.117 days) were identified radiochemically. One can estimate the transmutation cross section (n, γ) in the given neutron field as σ( 129 I(n, γ))=(10±2)b and σ( 237 Np(n, γ))=(140±30)b. The experiments were carried out in November 1996 at the Synchrophasotron, Laboratory of High Energies (LHE), Dubna, Russia

Phase equilibrium in the AgI-RbI-H2O system at 25 deg C

International Nuclear Information System (INIS)

Stepin, B.D.; Serebrennikova, G.M.; Sazikova, L.A.; Starikova, Z.A.

1977-01-01

The triple system of AgI-RbI-H 2 O at 25 deg C was studied by the isothermal method. The formation of the Rb 2 AgI 3 complex compound, which dissolves in water with decomposition, was established. A powder pattern of Rb 2 AgI 3 was indexed

Combustion/absorption process for the separation of {sup 14}C and {sup 3}H in radwastes released from nuclear power plants and their analysis

Energy Technology Data Exchange (ETDEWEB)

Ko, Young Gun, E-mail: ygko@kaeri.re.kr; Kim, Chang-Jong; Cho, Young Hyun; Chung, Kun Ho; Kang, Mun Ja

2017-06-05

Highlights: • {sup 14}CO{sub 2} and THO were produced by the combustion of radwaste samples. • The radioactivity of {sup 14}CO{sub 2} and THO absorbed sorbents were measured by LSC. • The CO{sub 2} absorption in the {sup 14}C sorbent was analyzed using by FT-IR and a rheometer. • The temperature and viscosity of the CO{sub 2} absorbed {sup 14}C sorbent was investigated. - Abstract: Radioactivities of {sup 3}H and {sup 14}C in spent radioactive ion exchange resins and spent radioactive lubricant oils released from nuclear power plants, has been determined using a combustion and sorption method (combustion method). The liquid scintillation counting (LSC) spectra showed that the interference of other radionuclides has not significantly affected the determination of radioactivities of {sup 3}H and {sup 14}C in the radwaste samples. The chemical structure of {sup 14}CO{sub 2}, which originated from the combustion of radwastes, trapped {sup 14}C sorbent has been investigated using Fourier transform infrared spectroscopy (FT-IR). FT-IR study showed interesting results that peaks for uncoupled CO{sub 2} and carbonic amide appeared at FT-IR spectra of CO{sub 2} high-absorbed {sup 14}C sorbents, while the peak for carbamate was only observed at the spectra of CO{sub 2} low-absorbed sorbents. During the CO{sub 2} sorption in {sup 14}C sorbent, temperature and viscosity of the sorbent increased owing to decrease of enthalpy and increase of apparent molecular weight of the sorbent caused by the bonding formation between sorbent molecules.

Synthesis of C-9-14C-1,8-dihydroxy-3-carboxyanthraquinone

International Nuclear Information System (INIS)

De Witte, P.; Lemli, J.

1988-01-01

The synthesis of C-9- 14 C-rhein is reported using 14 CO 2 as a 14 C-source. After preparing 14 C-1, 8-dimethoxy-3-methylanthraquinone by a condensation reaction, the product is demethylated and the 3-methyl group converted to the corresponding 3-carboxy group. The radio-active yield of the total synthesis, starting with 1 Ci 14 CO 2 is 6,9% (6, 9 mCi); 352 mg 14 rhein is produced with a specific activity of 55,7 mCi/mmol. (author)

A summary of global {sup 129}I in marine waters

Energy Technology Data Exchange (ETDEWEB)

He Peng, E-mail: peng.he@geo.uu.se [Dept. of Earth Sciences, Uppsala University, Villav. 16, 752 36 Uppsala (Sweden); Aldahan, A. [Dept. of Earth Sciences, Uppsala University, Villav. 16, 752 36 Uppsala (Sweden); Dept. of Geology, United Arab Emirates University, P.O. Box 17551, Al Ain (United Arab Emirates); Possnert, G. [Tandem Laboratory, Uppsala University, P.O. Box 529, 751 20 Uppsala (Sweden); Hou, X.L. [Riso National Laboratory for Sustainable Energy, NUK-202, Technical University of Denmark, DK-4000 Roskilde (Denmark)

2013-01-15

Despite the many investigations concerning the occurrence of anthropogenic iodine-129 in the atmosphere, terrestrial and marine environments, there is a lack of a comprehensive collection of data on the distribution of the isotope in marine waters. The temporal and spatial variability of anthropogenic {sup 129}I is strongly linked to the major point sources in the Irish Sea and the English Channel and the global marine spreading pathways are partly outlined from these sources. The temporal evolution is still, however, not well defined when transport and dissipation are considered in the different oceans and ocean compartments. We here summarize available published literature data on {sup 129}I temporal and spatial distribution in the global marine water. The results show presence of numerous data sets for the North Atlantic and Arctic Oceans where strong variability in terms of water depth, time and location also occur. Scarcity of data on {sup 129}I from the Pacific, Indian and South Atlantic Oceans demonstrates gaps in the coverage of the isotope spatial extent. These shortcomings in the spatial coverage may relate to the understanding that the anthropogenic {sup 129}I signal will take a long time to be transported, if at all, from the North Atlantic into other oceans. Data from recent expeditions in the Southern oceans and the Geotraces ocean profiling will reveal additional information about {sup 129}I distribution in the marine waters.

129I in the oceans. Origins and applications

International Nuclear Information System (INIS)

Raisbeck, G.M.; Yiou, F.

1999-01-01

The quantity of the long lived (half-life 15.7 million years) radioactive isotope 129I in the pre-nuclear age ocean was =100 kg. Various nuclear related activities, including weapons testing, nuclear fuel reprocessing, Chernobyl and other authorized or non-authorized dumping of radioactive waste have increased the ocean inventory of 129I by more than one order of magnitude. The most important of these sources are the direct marine discharges from the commercial reprocessing facilities at La Hague (France) and Sellafield (UK) which have discharged -1640 kg in the English Channel, and =720 kg in the Irish Sea, respectively. We discuss how this 129I can be used as both a 'pathway' and 'transit time' tracer in the North Atlantic and Arctic oceans, as well as a parameter for distinguishing between reprocessed and non-reprocessed nuclear waste in the ocean, and as a proxy for the transport and dilution of other soluble pollutants input to the North Sea

129I in the oceans: origins and applications.

Science.gov (United States)

Raisbeck, G M; Yiou, F

1999-09-30

The quantity of the long lived (half-life 15.7 million years) radioactive isotope 129I in the pre-nuclear age ocean was approximately 100 kg. Various nuclear related activities, including weapons testing, nuclear fuel reprocessing, Chernobyl and other authorized or non-authorized dumping of radioactive waste have increased the ocean inventory of 129I by more than one order of magnitude. The most important of these sources are the direct marine discharges from the commercial reprocessing facilities at La Hague (France) and Sellafield (UK) which have discharged approximately 1640 kg in the English Channel, and approximately 720 kg in the Irish Sea, respectively. We discuss how this 129I can be used as both a 'pathway' and 'transit time' tracer in the North Atlantic and Arctic oceans, as well as a parameter for distinguishing between reprocessed and non-reprocessed nuclear waste in the ocean, and as a proxy for the transport and dilution of other soluble pollutants input to the North Sea.

Labeling of 3H11 With 123I and Its Biodistribution

International Nuclear Information System (INIS)

Qin Hongbin; Yin Wei; Gao Huibo; Chen Daming; Qi Benzhong; Jin Xiaohai; Bai Hongsheng; Zhang Wenhui; Yang Zhi

2010-01-01

3H11 was labeled with 123 I by Iodogen method,and the labeling product were purified with PD-10 column. The labeling yield and the radiochemical purity of the product was determined by paper chromatography. The biodistribution of 123 I-3H11 in normal mice was car ride out as well. The optimal experimental conditions of 123 I-3H11 was as follow: Iodogen 10 μg, 3H11 30 μg, Na 123 I solution 20 μL (13.3 MBq), PBS 100 μL (pH 7.4, 0.2 mol/L), the normal temperature for 8 min. The labeling yield of 123 I-3H11 was 70%-80%. After stored at 4 degree C for 48 h in human serum,the radiochemical purity was more than 92%. The results of biodistribution showed that the clearance of radiolabeled antibody in blood (half time, T 1/2 ) was 12.25±0.25 h, and the radioactivity in the stomach was up taken obviously. The above results indicated that 123 I-3H11 appears to show some potential as gastric cancer imaging diagnostic agent. (authors)

9 CFR 3.129 - Feeding.

Science.gov (United States)

2010-01-01

... Warmblooded Animals Other Than Dogs, Cats, Rabbits, Hamsters, Guinea Pigs, Nonhuman Primates, and Marine... 9 Animals and Animal Products 1 2010-01-01 2010-01-01 false Feeding. 3.129 Section 3.129 Animals and Animal Products ANIMAL AND PLANT HEALTH INSPECTION SERVICE, DEPARTMENT OF AGRICULTURE ANIMAL...

Speciation Analysis and Environmental Tracer Studies of ¹²⁹I

DEFF Research Database (Denmark)

Zhang, Luyuan

, Japan were investigated. Iodate for both 129I and 127I is the predominant form for the seawater in the central Arctic and Greenland coast, whereas iodide is the major specie of 129I and 127I in Danish coast. A distinct distribution pattern of iodine species was observed in Fukushima offshore seawater......, such as the Greenland Sea, and the western Atlantic Ocean, as well as to the atmosphere and the Arctic ecosystem. Aerosol samples collected at two locations (Risø, Denmark, a coastal site, and Tsukuba Japan, about 170 km southwest of the Fukushima Dai-ichi nuclear power plant) during spring 2011 (shortly after...... in real samples demonstrate that the developed method is reliable for accurate determination of 129I and 127I species in aerosol samples. Distributions of chemical species (iodide and iodate) of 129I and 127I in the seawater from the central Arctic, Greenland coast, Danish coast and offshore Fukushima...

Rh(I) -Catalyzed Intramolecular Carbonylative C-H/C-I Coupling of 2-Iodobiphenyls Using Furfural as a Carbonyl Source.

Science.gov (United States)

Furusawa, Takuma; Morimoto, Tsumoru; Nishiyama, Yasuhiro; Tanimoto, Hiroki; Kakiuchi, Kiyomi

2016-08-19

Synthesis of fluoren-9-ones by a Rh-catalyzed intramolecular C-H/C-I carbonylative coupling of 2-iodobiphenyls using furfural as a carbonyl source is presented. The findings indicate that the rate-determining step is not a C-H bond cleavage but, rather, the oxidative addition of the C-I bond to a Rh(I) center. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Anthropogenic {sup 129}I in the North Pacific, Bering and Chukchi Seas, and Arctic Ocean in 2012–2013

Energy Technology Data Exchange (ETDEWEB)

Nagai, H., E-mail: hnagai@chs.nihon-u.ac.jp [Department of Chemistry, College of Humanities and Sciences, Nihon University, Tokyo 156-8550 (Japan); Hasegawa, A. [Graduate School of Integrated Basic Sciences, Nihon University, Tokyo 156-8550 (Japan); Yamagata, T. [Department of Chemistry, College of Humanities and Sciences, Nihon University, Tokyo 156-8550 (Japan); Kumamoto, Y.; Nishino, S. [Japan Agency for Marine-Earth Science and Technology, Kanagawa 237-0061 (Japan); Matsuzaki, H. [Department of Nuclear Engineering and Management, The University of Tokyo, Tokyo 113-0032 (Japan)

2015-10-15

Most of anthropogenic {sup 129}I in marine environment are due to discharge from the nuclear fuel reprocessing facilities at Sellafield (U.K.) and La Hague (France) for past few decades. The discharge raised {sup 129}I concentration in seawaters in the North Atlantic and Arctic Oceans to more than 10{sup 9} atoms L{sup −1}, which is two orders of magnitude higher than that in other region. Recently, in March 2011, a large quantity of {sup 129}I was released into the western North Pacific due to the Fukushima Daiichi Nuclear Power Plant (F1NPP) accident. To evaluate the influence of these events, we have measured {sup 129}I concentration in seawaters in the northern North Pacific Ocean, Bering and Chukchi Seas, and Arctic Ocean in 2012–2013. The {sup 129}I concentrations were 1.0–1.8 × 10{sup 7} atoms L{sup −1} in the surface waters in the vicinity of 47°N 150°E–130°W North Pacific Ocean, Bering Sea, and Chukchi Sea (<74°N), which are equal to or lower than the {sup 129}I concentration level in surface water in the North Pacific Ocean before the F1NPP accident. The vertical profiles in the North Pacific were almost same as that observed in the western North Pacific before the F1NPP accident. The {sup 129}I distribution in seawater in the North Pacific to the Chukchi Sea revealed no significant increase of {sup 129}I concentration caused by the F1NPP accident. The {sup 129}I concentrations were 13–14 × 10{sup 7} atoms L{sup −1} in surface waters and 80 × 10{sup 7} atoms L{sup −1} at depths of 300 and 800 m in the Arctic Ocean.

Origin of I in soil and the 129I problem

International Nuclear Information System (INIS)

Cohen, B.L.

1985-01-01

It is widely believed that the I in soil is derived from the I in oceans by evaporating-atmospheric transport-washout by rain over land, rather than from the I in rock when the latter is weathered into soil. Since human I burdens are derived largely from soil by plant root uptake into food, this implies that the specific activity of 129 I in the I of human thyroids will be the same as that in the oceans, whereas it would be similar to that in rock (much lower) if the I in soil were derived from weathering of rock as is the case for other heavy trace elements. The bases for the oceanic origin theory are analyzed and found not to be in accord with modern data. Recent data shows no correlation between concentration of I in soil and proximity to oceans, which argues strongly against the oceanic origin theory. Some problems with long-distance atmospheric transport are pointed out. It is concluded that only a small fraction of the I in soils is of oceanic origin. Most estimates of very long-term effects of 129 I on human health are therefore several times too high

Relationship between HCO_3"- concentration to weight of C_6H_6 of environmental isotop "1"4C analysis and its relationship with sampling in the field

International Nuclear Information System (INIS)

Satrio; Rasi Prasetio

2016-01-01

It has been done the groundwater sampling process of deep aquifer in Jakarta and surrounding areas for the analysis of environmental isotope "1"4C. Groundwater sampling was preceded by calculating the concentration of HCO_3"- (bicarbonate ion) through titration in the field. The number of repetitions of sampling is determined by the concentration data of HCO_3"- which obtained. The Repetition of this sampling will determine the acquisition of a solution of C_6H_6 (benzene) during the synthesis process benzene. In the field, the sampling is done by extracting of 60 liters of water to precipitate BaCO_3. The sampling process is repeated based on data from the bicarbonate ion concentration. The purpose of this study to determine the relationship between the concentration of HCO_3"- to the weights C_6H_6 which obtained in the analysis of environmental isotope "1"4C and evaluate the number of repetitions of the sampling that should be done. Based on the analysis of titration in the field, shows that concentration HCO_3"- ranged between 180 - 600 ppm with the acquisition of benzene between 1.84 to 4.5 grams. There is a strong relationship between the concentration of HCO_3"- and C_6H_6 weights obtained in the process of synthesis of benzene with a correlation of about 0.900. This correlation can be improved by measuring the concentration of HCO_3"- in advance in the laboratory tend to be more accurate than in the field. (author)

Searches for Lorentz violation in {sup 3}He/{sup 129}Xe clock comparison experiments

Energy Technology Data Exchange (ETDEWEB)

Allmendinger, F. [Universitaet Heidelberg, Physikalisches Institut (Germany); Burghoff, M. [Physikalisch-Technische Bundesanstalt (Germany); Heil, W., E-mail: wheil@uni-mainz.de; Karpuk, S. [Johannes-Gutenberg Universitaet, Institut fuer Physik (Germany); Kilian, W.; Knappe-Grueneberg, S.; Mueller, W. [Physikalisch-Technische Bundesanstalt (Germany); Schmidt, U. [Universitaet Heidelberg, Physikalisches Institut (Germany); Schnabel, A.; Seifert, F. [Physikalisch-Technische Bundesanstalt (Germany); Sobolev, Yu [Johannes-Gutenberg Universitaet, Institut fuer Physik (Germany); Trahms, L. [Physikalisch-Technische Bundesanstalt (Germany); Tullney, K. [Johannes-Gutenberg Universitaet, Institut fuer Physik (Germany)

2013-03-15

We discuss the design and performance of a very sensitive low-field magnetometer based on the detection of free spin precession of gaseous, nuclear polarized {sup 3}He or {sup 129}Xe samples with a SQUID as magnetic flux detector. Characteristic spin precession times T{sub 2}{sup Asterisk-Operator} of up to 115 h were measured in low magnetic fields (about 1 {mu}T) and in the regime of motional narrowing. With the detection of the free precession of co-located {sup 3}He/{sup 129}Xe nuclear spins (clock comparison), the device can be used as ultra-sensitive probe for non-magnetic spin interactions, since the magnetic dipole interaction (Zeeman-term) drops out in the weighted frequency difference, i.e., {Delta}{omega} = {omega}{sub He} - {gamma}{sub He}/{gamma}{sub Xe}{center_dot}{omega}{sub Xe}. We report on searches for Lorentz violating signatures by monitoring the Larmor frequencies of co-located {sup 3}He/{sup 129}Xe spin samples as the laboratory reference frame rotates with respect to distant stars (sidereal modulation).

Speciation analysis of 129I in seawater using coprecipitation and accelerator mass spectrometry and its applications

DEFF Research Database (Denmark)

Xing, Shan; Hou, Xiaolin; Aldahan, Ala

2017-01-01

Speciation analysis of long-lived 129I in seawater can provide useful information on the source of water masses. This paper presents an improved method for speciation analysis of 129I based on coprecipitation of iodide as AgI with Ag2SO3 and AgCl. By adding a small amount of 127I carrier...

High pressure 129I Moessbauer studies of GeI4 molecular crystals

International Nuclear Information System (INIS)

Pasternak, M.P.; Taylor, R.D.

1989-01-01

The Moessbauer effect in 129 I in conjunction with Diamond-Anvil-Cell high pressure techniques was applied to investigate the high pressure phase(s) of the molecular crystal GeI 4 . The 129 I Quadrupole Interaction was the main probe for characterizing the intermolecular structural transformation with pressure. With increasing pressure, at about 15 GPAa, the onset of a partial molecular-association phase (HP1) is first observed. In HP1 two out of the four iodines strongly overlap to form linear chains of GeI 4 . The HP1 phase coexists with the low pressure (LP) molecular phase, but its population increases with increasing pressure. At P ∼20 GPa a second high pressure phase (HP2) is identified where all four iodines strongly overlap to form a three dimensional, fully molecular-associated structure. With increasing pressure and at P > 20 GPa, HP2 is the only phase up to P = 34 GPa, the highest pressure used. A significant hysteresis of the relative abundances with pressure is observed. The isomer shift of the HP2 and HP1 structures is considerably larger than that of the LP one. 11 refs., 3 figs

The role of {sup 129} I in the environment and its measurement at the ANTARES AMS center

Energy Technology Data Exchange (ETDEWEB)

Fink, D.; Hotchkis, M.; Lawson, E.M.; Jacobsen, G.E. [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

1996-12-31

Anthropogenic production of several radionuclides during the nuclear era has resulted in a dramatic enhancement in their ambient concentrations relative to cosmogenic values for geophysical systems which are in exchange with the atmosphere and oceans. These environmental pulses have been archived in sediments and polar ice caps where for example profiles of {sup 90}Sr and {sup 135}Cs have been measured to establish global transport rates and deposition budgets for bomb-test products. {sup 129}I, half-life 16 Ma, is another nuclear fission product that is and has been periodically released into the atmosphere, but unlike the shorter lived {sup 90}Sr and {sup 135}Cs, had not found widespread utilization because previous detection via neutron activation analysis ({sup 129}I (2n,{gamma}){sup 131}I) was cumbersome and lacked the required sensitivity. AMS has resolved this problem for {sup 129}I measurements by reducing the required sample size, measurement time and atom-counting sensitivity to as little as 10{sup 6} atoms that enable {sup 129}I/{sup 127}I isotopic ratios as low as 2x10-{sup 14} to be measured on milligram samples within an hour. As a result of this new detection capability, an ever-growing interest and awareness in the application of {sup 129}I as an environmental tracer, radiometric dating tool and monitor of operations of the nuclear industry has been generated. 7 refs.

The role of {sup 129} I in the environment and its measurement at the ANTARES AMS center

Energy Technology Data Exchange (ETDEWEB)

Fink, D; Hotchkis, M; Lawson, E M; Jacobsen, G E [Australian Nuclear Science and Technology Organisation, Lucas Heights, NSW (Australia)

1997-12-31

Anthropogenic production of several radionuclides during the nuclear era has resulted in a dramatic enhancement in their ambient concentrations relative to cosmogenic values for geophysical systems which are in exchange with the atmosphere and oceans. These environmental pulses have been archived in sediments and polar ice caps where for example profiles of {sup 90}Sr and {sup 135}Cs have been measured to establish global transport rates and deposition budgets for bomb-test products. {sup 129}I, half-life 16 Ma, is another nuclear fission product that is and has been periodically released into the atmosphere, but unlike the shorter lived {sup 90}Sr and {sup 135}Cs, had not found widespread utilization because previous detection via neutron activation analysis ({sup 129}I (2n,{gamma}){sup 131}I) was cumbersome and lacked the required sensitivity. AMS has resolved this problem for {sup 129}I measurements by reducing the required sample size, measurement time and atom-counting sensitivity to as little as 10{sup 6} atoms that enable {sup 129}I/{sup 127}I isotopic ratios as low as 2x10-{sup 14} to be measured on milligram samples within an hour. As a result of this new detection capability, an ever-growing interest and awareness in the application of {sup 129}I as an environmental tracer, radiometric dating tool and monitor of operations of the nuclear industry has been generated. 7 refs.

New Resin for the Selective Extraction of {sup 129}I

Energy Technology Data Exchange (ETDEWEB)

Bombard, A.; Happel, S. [TrisKem International, Bruz (France); Zulauf, A. [NUKEM Technologies GmbH, Alzenau (Germany); Streng, R. [Radiochemistry, Department of Chemistry, Philipps-University Marburg, Marburg (Germany)

2013-07-15

{sup 129}I is an ideal tracer of the marine environment. It has been used for some years particularly in the northeast Atlantic, Nordic seas and Arctic to determine its distribution after its discharges from La Hague and Sellafield reprocessing plants. Various methods for {sup 129}I determination exist. A new resin selective for iodine has been developed, characterized and tested on environmental samples. In order to allow {sup 129}I determination and to obtain accurate and precise results, the samples have to pass a number of sample preparation steps; among these steps are chemical separation and purification. The results of the analysis of seawater samples are presented. (author)

C-H and H-H Bond Activation via Ligand Dearomatization/Rearomatization of a PN3P-Rhodium(I) Complex

KAUST Repository

Huang, Kuo-Wei; Wang, Yuan; Zheng, Bin; Pan, Yupeng; Pan, Chengling; He, Lipeng

2015-01-01

A neutral complex PN3P-Rh(I)Cl (2) was prepared from a reaction of the PN3P pincer ligand (1) with [Rh(COD)Cl]2 (COD = 1,5-cyclooctadiene). Upon treatment with a suitable base, H–H and Csp2–H activation reactions can be achieved through

Carrier phases for iodine in the Allende meteorite and their associated 129Xer/127I ratios: A laser microprobe study

International Nuclear Information System (INIS)

Kirschbaum, C.

1988-01-01

A new mass spectrometer of high sensitivity coupled to a laser microprobe sample extraction system was used to determine the 129 Xe r /I ratios of minerals which carry 129 Xe r in the Allende meteorite. In sodalite-rich fine-grained inclusions Ok correlates with Cl verifying that sodalite carries the majority of I. One sample heated above the decomposition point of sodalite had a small amount of residual I indicating the presence of at least one other carrier. The Cl/I ratio of the matrix was different from that of the fine-grained inclusions and the 129 Xe r correlates with trapped Xe. This implies either a different Cl/I ratio for sodalite in the matrix or a different carrier for I in matrix. In melilite from one coarse-grained inclusion, I is variable and correlates with both Xe and, surprisingly, 131 Xe produced from Ba during the irradiation. In coarse-grained inclusions with Cl-rich alteration products in cracks, most of the 129 Xe r is found in those cracks. A residual amount of 129 Xe r is present in melilite samples which show no Cl-rich alteration products, and is a trace impurity in the melilite. The 129 Xe r / 127 I ratio of sodalite from the fine-grained inclusions, and matrix is similar--between 1.25 and 1.35 x 10 -4 . This implies an age for these samples within 2 million years of a Bjurbole chondrule included in the irradiation as a standard. The 129 Xe r / 127 I ratio of a sample of a fine-grained inclusion heated to 1,100 degree C is 2.4 x 10 -4 or 16 million years before the Bjurbole chondrule. A coarse-grained inclusion on the other hand showed a 129 Xe r / 127 I ratio of 3.15 x 10 -5 or 35 million years after the Bjurbole chondrule

The synthesis of taurine-conjugated bile acids and bile acid sulfates labeled with 14C or 3H in the taurine moiety

International Nuclear Information System (INIS)

Jie Zhang; Griffiths, W.J.; Sjoevall, Jan

1997-01-01

Studies of bile acid transport systems require radio-labeled taurine-conjugated bile acids with high specific activity. An established procedure was optimized to provide mild, fast, and effective conjugation of radio-labeled taurine with different types of bile acids, including those with labile 7α-hydroxy-3-oxo-Δ 4 or 3β, 7α-dihydroxy-Δ 5 structures. Taurine labeled with 14 C or 3 H was reacted with excess bile acid anhydride formed from the tributylamine salt and ethylchloroformate (2/1 M/M) in aqueous dioxane for 15 min at room temperature. The yields were higher than 95% and less than 2% side products were formed. Bile acid sulfates were conjugated with 14 C- or 3 H-labeled taurine by using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline as the coupling reagent. The products were effectively purified by chromatography of the sodium salts on Sephadex LH-20. The yields of taurine-conjugated bile acid sulfates were 65-70%. (author)

Effect of tolbutamide on 14C-sodium bicarbonate and 14C-alanine metabolism in isolated rat hepatocytes

International Nuclear Information System (INIS)

Kunjathoor, V.V.; Ye, Y.; Pillai, U.A.; Ferguson, P.W.; Medon, P.J.

1990-01-01

Tolbutamide (TOLB) is a sulfonylurea commonly used in the treatment of noninsulin-dependent diabetes mellitus. Studies have shown that TOLB affects gluconeogenesis and glycolysis from various substrates in the liver. Specifically, TOLB inhibits gluconeogenesis from lactate in a dose-dependent manner. In order to further clarify tolbutamide's mechanism of action, its effect on the incorporation of 14 C from NaH 14 CO 3 and 14 C-alanine into glucose, lactate or pyruvate in the presence of lactate was measured. Rat hepatocytes were incubated with lactate (2.0 mM) with or without TOLB (1.0 mM) in the presence of NaH 14 CO 3 or 14 C-alanine. TOLB inhibited the incorporation of C 14 from NaHCO 3 and alanine into glucose by 55 and 56%, respectively. TOLB did not alter the incorporation of C 14 from NaHCO 3 into lactate or pyruvate. TOLB did not affect the incorporation of 14 C from alanine into lactate but produced a pooling of 14 C as pyruvate. The authors data support studies demonstrating the TOLB produces its actions, in part, by increasing the concentration of fructose-2,6-bisphosphate and inhibiting pyruvate carboxylase

Photochemically activated antiviral halogenated 1,8-naphthalimides: synthesis of N,N'-bis-{2-[(5-bromo-2-[1-14C]hexyl-1H-benz[de]isoquinolin-1,3(2H)-dion-6-yl)amino]ethyl}hexanediamide

International Nuclear Information System (INIS)

Hayes, B.A.; Gupta, Surendra; Shaochieh Chang; Utecht, R.E.; Lewis, D.E.

1996-01-01

The synthesis of N,N'-bis-{2-[(5-bromo-2-[1- 14 C]hexyl-1H-benz[de]isoquinolin-1, 3(2H)-dion-6-yl)amino]ethyl}hexanediamide from 1-[1- 14 C]-hexylamine and 4-chloro-1,8-naphthalic anhydride is described. The anhydride is first converted to the 4-chloro-n-[1- 14 C]hexyl-1,8-naphthalimide by condensation with 1-[1- 14 C]-hexylamine, and the chlorine is then displaced with ethylenediamine to give the 4-(2-aminoethylamino-N-[1- 14 C]hexyl-1,8-naphthalimide. Coupling of this monomeric naphthalimide with adipoyl chloride affords the dimeric naphthalimide which is brominated regiospecifically with elemental bromine in carbon tetrachloride to afford the title compound. (author)

Use of [2-14C]mevalonate and saponin-bound [14C]-3-hydroxy-3-methylglutaric acid for the biosynthesis of terpenoids in leaves of Dioscorea deltoidea

International Nuclear Information System (INIS)

Gurielidze, K.G.; Paseshnichenko, V.A.; Vasil'eva, I.S.

1986-01-01

After the introduction of [2- 14 C]acetate into leaves of Dioscorea deltoidea, a radioactive furonanalog of deltafolin - protodeltofolin, containing two-thirds of the label in the 3-hydroxy-3-methylglutaryl portion - was isolated from them. Radioactive β-careotene and sterols were isolated from cut young leaves of Dioscorea 24 h after the introduction of [ 14 C] protodeltofolin into them, using chromatography on a column of silica gel and precipitation of sterols in the form of digitonins for this purpose. The incorporation of radioactivity from [ 14 C]-3-hydroxy-3-methyl-glutaric acid, bound in the form of a saponin, and β-carotene came to 0.18-0.80%, while incorporation into sterols came to 0.07-2.86% of the radioactivity of the alcohol extract. Thereby it was shown that 3-hydroxyl-3-methylglutaric acid, bound in the form of the saponin, can be used to form terpenoids in Dioscorea leaves. It was suggested that the binding of hydroxymethylglutaric acid to saponin represents one of the mechanisms of regulation of the rate of terpenoid biosynthesis in Dioscorea leaves

14C tebuconazole degradation in Colombian soils.

Science.gov (United States)

Mosquera, C S; Martínez, M J; Guerrero, J A

2010-01-01

Tebuconazole is a fungicide used on onion crops (Allium Fistulosum L) in Colombia. Persistence of pesticides in soils is characterized by the half-life (DT50), which is influenced by their chemical structure, the physical and chemical properties of the soil and the previous soil history. Based on its structural and chemical properties, tebuconazole should be expected to be relatively persistent in soils. Laboratory incubation studies were conducted to evaluate persistence and bond residues of 14C tebuconazole in three soils, two inceptisol (I) and one histosol (H). Textural classifications were: loam (101), loamy sand (102) and loam (H03), respectively. Data obtained followed a first-order degradation kinetics (R2 > or = 0.899) with DT50 values between 158 and 198 days. The production of 14CO2 from the 14C-ring-labelled test chemicals was very low and increased slightly during 63 days in all cases. The methanol extractable 14C-residues were higher than aqueous ones and both decreased over incubation time for the three soils. The formation of bound 14C-residues increased with time and final values were 11.3; 5.55 and 7.87% for 101, 102 and H03 respectively. Soil 101 showed the lowest mineralization rate and the highest bound residues formation, which might be explained by the clay fraction content. In contrast, an inverse behavior was found for soils 102 and H03, these results might be explained by the higher soil organic carbon content.

Discharges of [sup 14]C from nuclear facilities; Implication in environmental science

Energy Technology Data Exchange (ETDEWEB)

Iwakura, Tetsuo (Japan Chemical Analysis Center, Chiba (Japan))

1993-10-01

At present as C-14 existing in environment, there are that formed by cosmic ray in nature, by nuclear explosion experiment and released from nuclear facilities. As for the former two, the actual situation has been grasped, but the last one lacks the sure information as the range of its influence is local. In this study, the actual situation was explored based on the numerical evaluation of the amount generated in nuclear facilities and the investigative and analytical data by actual measurement. The rate of formation of natural C-14 is closely related to the variation of cosmic ray intensity and energy spectra. The specific radioactivity is 12.9 - 15.3 dpm/g, and it lowers due to the Suess effect, namely the increase of dead carbon. The C-14 due to nuclear explosion experiment reached the highest level of twice as much as the natural level in 1963, but thereafter, it decreased, and at present, it is 15-20% more than the natural level. The nuclear reaction and the reaction cross section of C-14 formation in LWRs, LMFBRs and HTGRs are shown. The formation of C-14 in fuel, core structures and cooling water of LWRs and in other types of reactors, and the examples of C-14 measurement around nuclear facilities are reported. (K.I.).

Kinetics of the reactions H+C2H4->C2H5, H+C2H5->2CH3 and CH3+C2H5->products studies by pulse radiolysis combined with infrared diode laser spectroscopy

DEFF Research Database (Denmark)

Sillesen, A.; Ratajczak, E.; Pagsberg, P.

1993-01-01

Formation of methyl radicals via the consecutive reactions H+C2H4+M-->C2H5+M (1) and H+C2H5-->CH3+CH3 (2a) was initiated by pulse radiolysis of 10-100 mbar H-2 in the presence of ethylene. The kinetics of CH3 Were studied by monitoring the transient infrared absorption at the Q(3, 3) line of the ...

Size of the z = 0.437 H I absorption region toward the QSO 3C 196

International Nuclear Information System (INIS)

Brown, R.L.; Benson, J.M.; Broderick, J.J.; Johnston, K.J.; Mitchell, K.J.

1988-01-01

VLBI spectral line observations made at the frequency of the z = 0.437 H I absorption line toward the extended radio QSO 3C 196 demonstrate that the absorption does not occur against the more compact continuum structure in this object. Apparently the H I absorption line results from absorption of the lower brightness continuum emission by an intervening cloud with an angular diameter which must be greater than 0.63 arcsec. For a standard cosmology, this corresponds to a linear extent greater than 2.25 kpc. For a spherical cloud, the mass of absorbing gas is near 7 x 10 to the 7th solar masses. Thus this particular QSO absorbing cloud is surprisingly large and massive. 22 references

Observation of radioactive iodine ({sup 131}I, {sup 129}I) in cropland soil after the Fukushima nuclear accident

Energy Technology Data Exchange (ETDEWEB)

Fujiwara, Hideshi, E-mail: hfuji@affrc.go.jp

2016-10-01

During the early stages of the Fukushima nuclear accident, the temporal variations of {sup 131}I deposited on the ground and of {sup 131}I accumulated in cropland soil were monitored at a fixed location in Japan. Moreover, concentrations of long-lived radioactive iodine ({sup 129}I) in atmospheric deposits and soil were measured to examine the feasibility of retrospectively reconstructing {sup 131}I levels from the levels of accident-derived {sup 129}I. The exceptionally high levels of {sup 131}I in deposits and soil were attributed to rainfall-related deposition of radionuclides. In the crop field studied, the losses of deposited {sup 131}I and {sup 129}I due to volatilization were small. The atomic ratio {sup 129}I/{sup 131}I in the topsoil corresponded to the same ratio in deposits. The {sup 131}I concentrations measured in the topsoil were very consistent with the {sup 131}I concentrations reconstructed from the {sup 129}I concentrations in the soil. - Highlights: • A high level of {sup 131}I contamination occurs through rainfall-related deposition. • Only a small loss of deposited radioactive iodine occurs via volatilization. • The {sup 129}I/{sup 131}I ratio in soil corresponds to the ratio in atmospheric deposit. • The feasibility of retrospectively reconstructing {sup 131}I is confirmed.

Role of leucine in isoprenoid metabolism. Incorporation of (3-/sup 13/C)leucine and of (2-/sup 3/H,4-/sup 14/C)-. beta. ,. beta. -dimethyl-acrylic acid into phytosterols by tissue cultures of Andrographis paniculata

Energy Technology Data Exchange (ETDEWEB)

Anastasis, P; Freer, I; Overton, K; Rycroft, D; Singh, S B [Glasgow Univ. (UK). Dept. of Chemistry

1985-02-01

(3-/sup 13/C)Leucine is incorporated into phytosterols by tissue cultures of Andrographis paniculata by breakdown to acetyl-CoA and its subsequent incorporation via (3S)-3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) and mevalonic acid; (2-/sup 3/H,4-/sup 14/C)-..beta..,..beta..-dimethylacrylic acid also is not incorporated intact.

Level and origin of {sup 129}I and {sup 137}Cs in lichen samples (Cladonia alpestris) in central Sweden

Energy Technology Data Exchange (ETDEWEB)

Gomez-Guzman, J.M., E-mail: jm_gomez@us.e [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain); Lopez-Gutierrez, J.M. [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain); Department of Applied Physics, University of Seville, C. Virgen de Africa 7, Seville 41011 (Spain); Holm, E. [Norwegian Radiation Protection Authority, Grini Naearingspark 13, P.O. Box 55, 1332 Osteras (Norway); Pinto-Gomez, A.R. [Centro Nacional de Aceleradores (CNA), Accelerator Mass Spectrometry Unit, Avd. Tomas Alva Edison 7, Isla de Cartuja, Seville 41092 (Spain)

2011-02-15

Lichen is a symbiosis between algae and fungi. They have for decades been used as bioindicators for atmospheric deposition of heavy metals, organic compounds and radioactive elements. Especially the species Cladonia alpestris and Cladonia rangiferina are important for the food chain lichen-reindeer-man. The concentration of {sup 129}I was determined in lichen samples (Cladonia alpestris) contaminated by fallout from atmospheric nuclear tests explosions and the Chernobyl accident. The samples were collected at Lake Rogen District (62.3{sup o}N, 12.4{sup o}E) in central Sweden in the periods 1961-1975 and 1987-1998, and analysed with accelerator mass spectrometry (AMS) at CNA (Seville) to study its distribution in different layers. Data on the {sup 137}Cs activity measured previously were also included in this study. The {sup 129}I concentration ranged from (0.95 {+-} 0.13) x 10{sup 8} at g{sup -1} in 1961 in the uppermost layer to (14.2 {+-} 0.5) x 10{sup 8} at g{sup -1} in 1987 in deepest layer. The {sup 129}I/{sup 137}Cs atom ratio ranged between 0.12 and 0.27 for lichen samples collected in the period 1961-1975, indicating weapons tests fallout. For lichen samples collected between 1987 and 1998 the behaviour of {sup 137}Cs concentrations reflected Chernobyl fallout. The concentrations of the two radionuclides followed each other quite well in the profile, reflecting the same origin for both. From the point of view of the spatial distribution in the lichen, it appears that {sup 129}I was predominantly accumulated in the lowest layer, the opposite to {sup 137}Cs for which the highest amounts were detected systematically in the topmost layer of lichen. This vertical distribution is important for radioecology because lichen is the initial link in the food chain lichen-reindeer-man, and reindeer only graze the upper parts of lichen carpets. - Research highlights: {yields} This work shows the results for {sup 129}I in lichens collected in 1961-1975 and 1987

A summary of global ¹²⁹I in marine waters

DEFF Research Database (Denmark)

He, Peng; Aldahan, A.; Possnert, G.

2013-01-01

of anthropogenic 129I is strongly linked to the major point sources in the Irish Sea and the English Channel and the global marine spreading pathways are partly outlined from these sources. The temporal evolution is still, however, not well defined when transport and dissipation are considered in the different...... and location also occur. Scarcity of data on 129I from the Pacific, Indian and South Atlantic Oceans demonstrates gaps in the coverage of the isotope spatial extent. These shortcomings in the spatial coverage may relate to the understanding that the anthropogenic 129I signal will take a long time...

5 alpha-Cholest-8(14)-en-3 beta-ol-15-one. In vivo conversion to cholesterol upon oral administration to a nonhuman primate

International Nuclear Information System (INIS)

Schroepfer, G.J. Jr.; Pajewski, T.N.; Hylarides, M.; Kisic, A.

1987-01-01

The metabolism of 5 alpha-cholest-8(14)-en-3 beta-ol-15-one (I), a potent inhibitor of cholesterol synthesis with marked hypocholesteremic activity, has been studied in a nonhuman primate. A mixture of [2,4- 3 H]-I and [4- 14 C]-cholesterol was administered to a male baboon in the form of a feedball. Blood was samples at 4, 8, 12, 16, and 24 hr. Detailed analyses of the plasma lipids indicated very rapid absorption of I (relative to cholesterol) and metabolism to cholesterol, cholesteryl esters, and esters of I. The labeled cholesterol was characterized by chromatographic techniques and by purification by way of its dibromide derivative. The levels of 3 H in plasma associated with I, esters of I, cholesterol, and cholesteryl esters each showed a different time course. By 24 hr after the administration of [2,4- 3 H]-I, most of the 3 H in plasma was associated with cholesterol and cholesteryl esters. The levels of total 3 H and 14 C in plasma at various times after the administration of the mixture of [2,4- 3 H]-I and [4- 14 C]-cholesterol differed markedly with 3 H showing a maximum value at 4 hr and 14 C showing a maximum value at 24 hr

Autoradiography of [14C]paraquat or [14C]diquat in frogs and mice: accumulation in neuromelanin

International Nuclear Information System (INIS)

Lindquist, N.G.; Larsson, B.S.; Lyden-Sokolowski, A.

1988-01-01

The herbicide paraquat has been suggested as a causative agent for Parkinson's disease because of its structural similarity to a metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP), which may induce a parkinsonism-like condition. MPTP as well as its metabolite 1-methyl-4-phenylpyridine have melanin affinity, and the parkinsonism-inducing potency of MPTP is much stronger in species with melanin in the nerve cells. Autoradiography of [ 3 H]MPTP in experimental animals has shown accumulation in melanin-containing tissues, including pigmented neurons. In the present whole body autoradiographic study accumulation and retention was seen in neuromelanin in frogs after i.p. injection of [ 14 C]paraquat or[ 14 C]diquat. By means of whole body autoradiography of [ 14 C]diquat in mice (a species with no or very limited amounts of neuromelanin) a low, relatively uniformly distributed level of radioactivity was observed in brain tissue. Accumulation of toxic chemical compounds, such as paraquat, in neuromelanin may ultimately cause lesions in the pigmented nerve cells, leading to Parkinson's disease

Glass-bonded iodosodalite waste form for immobilization of 129I

Science.gov (United States)

Chong, Saehwa; Peterson, Jacob A.; Riley, Brian J.; Tabada, Diana; Wall, Donald; Corkhill, Claire L.; McCloy, John S.

2018-06-01

Immobilization of radioiodine is an important requirement for current and future nuclear fuel cycles. Iodosodalite [Na8(AlSiO4)6I2] was synthesized hydrothermally from metakaolin, NaI, and NaOH. Dried unwashed sodalite powders were used to synthesize glass-bonded iodosodalite waste forms (glass composite materials) by heating pressed pellets at 650, 750, or 850 °C with two types of sodium borosilicate glass binders. These heat-treated specimens were characterized with X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, energy dispersive spectroscopy, thermal analysis, porosity and density measurements, neutron activation analysis, and inductively-coupled plasma mass spectrometry. For the best waste form produced (pellets mixed with 10 mass% of glass binder and heat-treated at 750 °C), the maximum possible elemental iodine loading was 19.8 mass%, but only ∼8-9 mass% waste loading of iodine was retained in the waste form after thermal processing. Other pellets with higher iodine retention either contained higher porosity or were incompletely sintered. ASTM C1308 and C1285 (product consistency test, PCT) experiments were performed to understand chemical durability under diffusive and static conditions. The C1308 test resulted in significantly higher normalized loss compared to the C1285 test, most likely because of the strong effect of neutral pH solution renewal and prevention of ion saturation in solution. Both experiments indicated that release rates of Na and Si were higher than for Al and I, probably due to a poorly durable Na-Si-O phase from the glass bonding matrix or from initial sodalite synthesis; however the C1308 test result indicated that congruent dissolution of iodosodalite occurred. The average release rates of iodine obtained from C1308 were 0.17 and 1.29 g m-2 d-1 for 80 or 8 m-1, respectively, and the C1285 analysis gave a value of 2 × 10-5 g m-2 d-1, which is comparable to or better than the durability of

Irradiation and gamma-ray spectrometric parameters for 129I neutron-activation analysis

International Nuclear Information System (INIS)

Brauer, F.P.; Strebin, R.S. Jr.; Mitzlaff, W.A.; Kaye, J.H.

1983-09-01

This paper describes the influence of reactor neutron irradiation facilities on low-level 129 I analysis methodology. Three reactors are compared - the HFIR at ORNL, the N-Reactor at Hanford, and a 1-MW research reactor at Washington State University, Pullman, WA. Parameters compared include sensitivity for 129 I and natural iodine and interference effects due to high levels of 127 I in irradiated samples. Selection of detector systems for off-site use at HFIR is discussed. A comparison of neutron activation analysis with other sensitive detection methods for measurement of 129 I is given

Superacid univalent metal phosphites (MH2PO3)2·H3PO3 (M Rb, Tl+) and MH2PO3·H3PO3 (M = K, Cs): synthesis and structure

International Nuclear Information System (INIS)

Kosterina, E.V.; Troyanov, S.I.; Aslanov, L.A.; Kemnits, Eh.

2001-01-01

Crystal superacid phosphites α-CsH 2 PO 3 ·H 3 PO 3 (1) and β-CsH 2 PO 3 ·H 3 PO 3 (2) were prepared by means of interaction between cesium carbonate and phosphoric acid excess. The structure of the compounds, i.e.: 1-rhombic crystal system, sp.gr. P2 1 2 1 2 1 , a = 6.033 (1), b = 6.444 (1), c = 18.345 (4) A: 2-monoclinic crystal system, sp.gr. C2/c, a = 9.990 (3), b = 12.197 (4), c = 6.866 (2) A, β = 118.14 (3) deg, was determined by the method of X-ray diffraction analysis of monocrystals at 150 K. Comparative analysis of the crystal structure and hydrogen bond systems in acid phosphites of different composition was conducted [ru

Do 14-3-3 proteins and plasma membrane H+-ATPases interact in the barley epidermis in response to the barley powdery mildew fungus?

DEFF Research Database (Denmark)

Finnie, C.; Andersen, C.H.; Borch, J.

2002-01-01

14-3-3 proteins form a family of highly conserved proteins with central roles in many eukaryotic signalling networks. In plants, they bind to and activate the plasma membrane H+-ATPase, creating a binding site for the phytotoxin fusicoccin. Barley 14-3-3 transcripts accumulate in the epidermis upon...... inoculation with the powdery mildew fungus. We have isolated a cDNA encoding a plasma membrane H+-ATPase (HvHA1), which is also induced by powdery mildew attack. The C-terminal domain of this H+-ATPase interacts with 14-3-3 proteins in the yeast two-hybrid system. Inoculation with the powdery mildew fungus......, or treatment with fusicoccin, results in an increase in fusicoccin binding ability of barley leaf membranes. Overlay assays show a fungus-induced increase in binding of digoxygenin-labelled 14-3-3 protein to several proteins including a 100 kDa membrane protein, probably the plasma membrane H...

Detection of radioactively labeled proteins is quenched by silver staining methods: quenching is minimal for 14C and partially reversible for 3H with a photochemical stain

International Nuclear Information System (INIS)

Van Keuren, M.L.; Goldman, D.; Merril, C.R.

1981-01-01

Silver staining methods for protein detection in polyacrylamide gels have a quenching effect on autoradiography and fluorography. This effect was quantitated for proteins in two-dimensional gels by microdensitometry using a computer equipped with an image processor and by scintillation counting of proteins solubilized from the gels. The original histologically derived silver stain had a quenching effect that was severe and irreversible for 3 H detection and moderate for 14 C detection. A silver stain based on photochemical methods had minimal quenching of 14 C detection and less of a quenching effect than the histological stain for 3 H detection. The 3 H quenching effect was partially reversible for the photochemical stain

Problems associated with scintillation counting of NaH14CO3 and gel suspension counting of Ba14CO3

International Nuclear Information System (INIS)

MacRae, J.C.; Wilson, S.

1978-01-01

Liquid NaH 14 CO 3 was assayed in emulsion-type (NE260 and Unisolve) and dioxan-based (NE250) scintillation cocktails contained in glass or polyethylene vials kept at 2 0 or 24-30 0 C. Different particle size ranges of standard Ba 14 CO 3 were assayed by gel suspension counting in Cabosil scintillation cocktail and in NE260 following solubilisation in EDTA-tetrasodium salt. Initial detectable activities of NaH 14 CO 3 in glass and polyethylene vials in NE250, NE260 and Unisolve were 97 and 96, 68 and 83, 71 and 89% of the true value respectively. Subsequent losses of activity over 7 days with the emulsion-type scintillators was greater from the polyethylene vials. Addition of phenylethylamine to the NE260 and Unisolve cocktails gave the true activity levels for all vials with no loss of activity over 6 days. When different particle size ranges of Standard Ba 14 CO 3 were suspended in Cabosil scintillation cocktail there was considerable variation in counting efficiency (77-88%) with little relationship between particle size and counting efficiency. The relationship between counting efficiency and channels ratio was not sufficiently precise for predictive purposes. Solubilisation of Ba 14 CO 3 in EDTA-tetrasodium salt gave similar counting efficiency and channels ratio values for all samples. (U.K.)

Study on Radioecology and Tracer of Iodine-129

International Nuclear Information System (INIS)

Xiaolin, Hou

2004-01-01

Chernobyl contaminated regions. The investigations show a strong dependence of childhood thyroid cancer incidence on thyroid exposure dose from short-lived radioiodine isotopes (i.e. 131 I, 133 I) released from the Chernobyl accident. However, the short half-life of 133 I (20.8 h) and 131 I (8.02 d) makes the evaluation of thyroid dose from these isotopes not easy. Due to the long half-life of 129 I, the 129 I concentration in environmental samples can be used to reconstruct the 131 I and 133 I dose to thyroids. Soil samples from areas in Belarus, Russia and Sweden contaminated by the Chernobyl accident were analysed for 129 I and 137 Cs by gamma-spectrometry. The atomic ratios of 129 I/ 137 Cs ranged from 0.10 to 0.30, with an average of 0.18. It confirmed that the 129 I/ 137 Cs ratios could be to reconstruct the deposition pattern of 131 I in these areas. (3) Application of I-129 as an oceanographic tracer. By analysing the time series seaweed samples collected from the coast of Denmark, Norway, and west Greenland, seawater samples from Baltic Sea, North Sea, Belt Sea, lake water from Denmark and other Baltic Seas for 129 I and 127 I, the transportation, mixing and water mass from North Sea to North Atlantic, Arctic and Baltic Sea and the origination of I-129 in the Baltic Sea were studied. (4) Chemical speciation of I-129. Seawater samples from in the North Sea, Kattegat and Baltic Sea were analyzed for 129 I and 127 I in both iodide and iodate species and total inorganic iodine. The possibility of using this method to study the geochemical cycle of iodine in the ocean was investigated. (author)

Density effects on high-n molecular Rydberg states: CH3I and C6H6 in H2 and Ar

International Nuclear Information System (INIS)

Asaf, U.; Felps, W.S.; Rupnik, K.; McGlynn, S.P.; Ascarelli, G.

1989-01-01

The absorption spectra of high-n Rydberg states of methyl iodide and benzene perturbed by varying number densities of hydrogen or argon, range 0.9x10 20 --10.5x10 20 cm -3 for H 2 and 0.6x10 20 --7.5x10 20 cm -3 for Ar, have been investigated. The high-n molecular states of both absorbers were found to shift linearly with the number density of atomic Ar and molecular H 2 scatterers. The Fermi formula modified by the Alekseev--Sobel'man polarization term provides an excellent fit of the shift data. The electron scattering lengths obtained are: 0.93 a 0 for H 2 and -1.63 a 0 for Ar using the CH 3 I absorber; and 0.99 a 0 for H 2 and -1.57 a 0 for Ar using the C 6 H 6 absorber. The electron scattering lengths for H 2 and Ar agree with the results of an empirical model that correlates scattering lengths and the polarizabilities α(spherical) for inert atoms and α 2 (nonspherical) for H 2 molecule

129I- and 99TcO4-scavengers for low level radioactive waste backfills

International Nuclear Information System (INIS)

Balsley, S.D.; Brady, P.V.; Krumhansl, J.L.; Anderson, H.L.

1997-03-01

Minimization of 129 I - and 99 TcO 4 - transport to the biosphere is critical to the success of low level radioactive waste (LLRW) storage facilities. Here we experimentally identify and classify optimal sorbent materials for inclusion in LLRW backfills. For low pH conditions (pH 4-5), Cu-sulfides and possibly imogolite-rich soils provide K d 's (surface-solution partition coefficients) of roughly 10 3 ml g -1 for iodide, and 10 2 ml g -1 for technetium. At near neutral pH, hydrotalcites, Cu-oxides, Cu-sulfides and lignite coal possess K d 's on the order of 10 2 ml g -1 for both iodine and technetium. At high pH (pH > 10), such as might occur in a cementitious LLRW facility, calcium monosulfate aluminate K d 's are calculated to be roughly 10 2 ml g -1 for both iodine and technetium

Labelling of glycerolipids in the cotyledons of developing oilseeds by [1-14C] acetate and brace2-3H] glycerol

International Nuclear Information System (INIS)

Slack, C.R.; Roughan, P.G.; Balasingham, N.

1978-01-01

3-sn-Phosphatidylcholine was identified as the major lipid in cotyledons from the developing seeds of soya bean, linseed and safflower when tissue was steamed before lipid extraction. Incubation for up to 3h changed the composition of this lipid and of diacylglycerol. Labelling studies, including pulse-chase experiments, were carried out with [1- 14 C] acetate and [2- 3 H] glycerol supplied to detached cotyledons. The results suggest a rapid turnover of 3-sn-phosphatidylcholine during triacylglycerol accumu-lation in developing oilseeds, and are consistent with the operation of a biosynthetic route whereby oleate initially esterified to the phospholipid is first desaturated, then polyunsaturated fatty acids transferred to triacylglycerol, via diacylglycerol. The possible role of oleoyl phosphatidylcholine as a substrate for oleate desaturation is discussed. (author)

He 3 -Xe 129 Comagnetometery using Rb 87 Detection and Decoupling

Science.gov (United States)

Limes, M. E.; Sheng, D.; Romalis, M. V.

2018-01-01

We describe a He 3 -Xe 129 comagnetometer using Rb 87 atoms for noble-gas spin polarization and detection. We use a train of Rb 87 π pulses and σ+/σ- optical pumping to realize a finite-field Rb magnetometer with suppression of spin-exchange relaxation. We suppress frequency shifts from polarized Rb by measuring the He 3 and Xe 129 spin precession frequencies in the dark, while applying π pulses along two directions to depolarize Rb atoms. The plane of the π pulses is rotated to suppress the Bloch-Siegert shifts for the nuclear spins. We measure the ratio of He 3 to Xe 129 spin precession frequencies with sufficient absolute accuracy to resolve Earth's rotation without changing the orientation of the comagnetometer. A frequency resolution of 7 nHz is achieved after integration for 8 h without evidence of significant drift.

1,4-Dihydroxyquinoxaline-2,3(1H,4H-dione

Directory of Open Access Journals (Sweden)

Wolfgang Frey

2008-03-01

Full Text Available The asymmetric unit of the title compound, C8H6N2O4, contains one half-molecule; a twofold rotation axis bisects the molecule. The quinoxaline ring is planar, which can be attributed to electron delocalization. In the crystal structure, intermolecular O—H...O hydrogen bonds link the molecules into R22(10 motifs, leading to layers, which interact via phenyl–phenyl interactions (C...C distances in the range 3.238–3.521 Å.

Secretin enhances [14C]erythritol clearance in unanesthetized dogs

International Nuclear Information System (INIS)

Lewis, M.H.; Baker, A.L.; Dhorajiwala, J.; Moossa, A.R.

1982-01-01

To determine the effect of secretin infusion on clearance of inert markers into bile, unanesthetized dogs fitted with Thomas cannulas received continuous infusions of [ 14 C]erythritol and [ 3 H]inulin throughout study. Taurocholic acid administered sequentially at 9.0, 20.0, and 40.0 mumol/min enhanced [ 14 C]erythritol clearance, and GIH secretin (3 units/min) administered along with TCA (40.0 mumol/min) increased [ 14 C]erythritol clearance from 4.9 +/- 1.2 ml/10 min to 6.8 +/- 1.3 ml/10 min (P less than 0.001), but simultaneously measured [ 3 H]inulin clearance was unaltered. Secretin alone also increased [ 14 C]erythritol clearance but did not alter [ 3 H]inulin clearance. The increase in [ 14 C]erythritol clearance per unit increase in bile flow was less during secretin infusion than TCA. Thus, secretin increases [ 14 C]erythritol transport through restricted channels, probably distal to the canaliculi. [ 14 C]Erythritol may not be an accurate marker for canalicular bile flow in dogs during secretin infusion

High-pressure phases of CuI studied by 129I-Moessbauer spectroscopy

International Nuclear Information System (INIS)

Kaindl, G.; Nowik, I.; Frank, K.H.

1992-01-01

The results of an 129 I-Moessbauer study of the high-pressure phases of CuI at 4.2 K and for external pressures up to 71 kbar are reported. The isomer shift S and the electric quadrupole interaction E q are found to undergo large discontinuities at the crystallographic phase-transition pressures of ≅18 kbar from zinc-blende to rhombohedral structure and at ≅46 kbar from rhombohedral to tetragonal. The pressure coefficients of these hyperfine parameters are significantly different for the three phases (zinc-blende; rhombohedral; tetragonal): dS/dP=-3.3; =+1.5; =+2.5x10 -3 mm/s/kbar. These results cannot be explained in terms of a simple molecular-orbital picture; instead, they reflect pressure-induced variations of the halogen-p/metal-d hybridization in the valence bands of the various phases of CuI. (orig.)

The I{sub c}(H)-T{sub c}(H) phase boundary of superconducting Nb thin films with periodic and quasiperiodic antidot arrays

Energy Technology Data Exchange (ETDEWEB)

Bothner, D.; Kemmler, M.; Cozma, R.; Kleiner, R.; Koelle, D. [Physikalisches Institut and Center for Collective Quantum Phenomena, Universitaet Tuebingen (Germany); Misko, V.; Peeters, F. [Departement Fysica, Universiteit Antwerpen (Belgium); Nori, F. [Advanced Science Institute, RIKEN (Japan)

2011-07-01

The magnetic field dependent critical current I{sub c}(H) of superconducting thin films with artificial defects strongly depends on the symmetry of the defect arrangement. Likewise the critical temperature T{sub c}(H) of superconducting wire networks is heavily influenced by the symmetry of the system. Here we present experimental data on the I{sub c}(H)-T{sub c}(H) phase boundary of Nb thin films with artificial defect lattices of different symmetries. For this purpose we fabricated 60 nm thick Nb films with antidots in periodic (triangular) and five different quasiperiodic arrangements. The parameters of the antidot arrays were varied to investigate the influence of antidot diameter and array density. Experiments were performed with high temperature stability ({delta}T<1 mK) at 0.5{<=}T/T{sub c}{<=}1. From the I-V-characteristics at variable H and T we extract I{sub c}(H) and T{sub c}(H) for different voltage and resistance criteria. The experimental data for the critical current density are compared with results from numerical molecular dynamics simulations.

Iodine Isotopes in Precipitation: Temporal Responses to 129I Emissions from the Fukushima Nuclear Accident

DEFF Research Database (Denmark)

Xu, Sheng; Freeman, Stewart P. H. T.; Hou, Xiaolin

2013-01-01

and the behavior of harmful radioiodine in the atmosphere, long-term precipitation samples have been collected over 2010–2012 at Fukushima, Japan for determination of long-lived 129I. It was observed that 129I concentrations of 1.2 × 108 atom/L in 2010 before the accident dramatically increased by ∼4 orders......The Fukushima Dai-ichi Nuclear Power Plant accident in 2011 has released a large amount of radionuclides to the atmosphere, and the radioactive plume has been dispersed to a large area in Europe and returned to Asia. To explore long-term trend of the Fukushima-derived radioactive plume...... environment. A 129I/131I atomic ratio of 16 ± 1 obtained from rainwater samples is comparable with a value estimated for surface soil samples. 129I results from Denmark suggest an insignificant effect of 129I released from Fukushima to the 129I levels in Europe....

Neutron activation and mass spectrometric measurement of /sup 129/I

International Nuclear Information System (INIS)

Strebin, R.S. Jr.; Brauer, F.P.; Kaye, J.H.; Rapids, M.S.; Stoffels, J.J.

1987-11-01

An integrated procedure has been developed for measurement of /sup 129/I by neutron activation analysis and mass spectrometry. An iodine isolation procedure previously used for neutron activation has been modified to provide separated iodine suitable for mass spectrometric measurement as well. Agreement between both methods has been achieved within error limits. The measurement limit by each method is about 10/sup 7/ atoms (2 fg) of /sup 129/I. 13 refs,. 4 figs., 1 tab

Preparation of arginine (guanide 14C)

International Nuclear Information System (INIS)

Pichat, L.; Baret, C.

1960-01-01

Reaction of anhydrous ammoniac at 800 deg. C on 14 CO 3 Ba gives rise to barium cyanamide 14 C with a yield of about 98 per cent. Addition on H 2 S on cyanamide 14 C leads to thiourea 14 C with a 85 per cent yield, which is quantitatively transformed into S-ethyl-isothiouronium iodide by treatment with methyl iodide. This 14 C-isothiouronium salt is used to introduce 14 C guanide group in α-N-tosyl-ornithine; tosyl group in α-N-tosyl-arginine thus obtained is then removed by hydrolysis with hydrochloric acid. Arginine is separated as flavianic acid salt and is purified on exchange resin Dowex-50. The overall yield based on 14 CO 3 Ba is 25 per cent. (author) [fr

Insect Ryanodine Receptor: Distinct But Coupled Insecticide Binding Sites for [N-C3H3]Chlorantraniliprole, Flubendiamide, and [3H]Ryanodine

OpenAIRE

Isaacs, André K.; Qi, Suzhen; Sarpong, Richmond; Casida, John E.

2012-01-01

Radiolabeled anthranilic diamide insecticide [N-C3H3]chlorantraniliprole was synthesized at high specific activity and compared with phthalic diamide insecticide flubendiamide and [3H]ryanodine in radioligand binding studies with house fly muscle membranes to provide the first direct evidence with a native insect ryanodine receptor that the major anthranilic and phthalic diamide insecticides bind at different allosterically coupled sites, i.e. there are three distinct Ca2+-release channel tar...

The synthesis of taurine-conjugated bile acids and bile acid sulfates labeled with {sup 14}C or {sup 3}H in the taurine moiety

Energy Technology Data Exchange (ETDEWEB)

Jie Zhang; Griffiths, W.J.; Sjoevall, Jan [Karolinska Inst., Medical Biochemistry and Biophysics Dept., Stockholm (Sweden)

1997-02-01

Studies of bile acid transport systems require radio-labeled taurine-conjugated bile acids with high specific activity. An established procedure was optimized to provide mild, fast, and effective conjugation of radio-labeled taurine with different types of bile acids, including those with labile 7{alpha}-hydroxy-3-oxo-{Delta}{sup 4} or 3{beta}, 7{alpha}-dihydroxy-{Delta}{sup 5} structures. Taurine labeled with {sup 14}C or {sup 3}H was reacted with excess bile acid anhydride formed from the tributylamine salt and ethylchloroformate (2/1 M/M) in aqueous dioxane for 15 min at room temperature. The yields were higher than 95% and less than 2% side products were formed. Bile acid sulfates were conjugated with {sup 14}C- or {sup 3}H-labeled taurine by using N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline as the coupling reagent. The products were effectively purified by chromatography of the sodium salts on Sephadex LH-20. The yields of taurine-conjugated bile acid sulfates were 65-70%. (author).

Iodine-129 measurements in soil samples from Dolon village near the Semipalatinsk nuclear test site.

Science.gov (United States)

Endo, Satoru; Tomita, Junpei; Tanaka, Kenichi; Yamamoto, Masayoshi; Fukutani, Satoshi; Imanaka, Tetsuji; Sakaguchi, Aya; Amano, Hikaru; Kawamura, Hidehisa; Kawamura, Hisao; Apsalikov, Kazbek N; Gusev, Boris I; Whitehead, Neil E; Shinkarev, Sergey; Hoshi, Masaharu

2008-07-01

Dolon village, located about 60 km from the border of the Semipalatinsk nuclear test site, is known to be heavily contaminated by the first USSR atomic bomb test in August 1949. Soil samples around Dolon were taken in October 2005 in an attempt to evaluate internal thyroid dose arising from incorporation of radioiodine isotopes (mainly (131)I). Iodine-129 in soil was measured by using the technique of accelerator mass spectrometry. The (129)I/(127)I atom ratios measured were in the range from 3.3 x 10(-9) to 3.3 x 10(-7). These values were within the range of the current background level ( approximately 10(-9) to 10(-7)) in the environment, including contributions from the global fallout of atmospheric nuclear tests and local fallout of nuclear facilities. The (129)I atom accumulated level in soil ranged from 1.28 x 10(13) to 1.59 x 10(14) atoms m(-2), the average (8.0 x 10(13)) of which was higher than the background level of (2-5) x 10(13). From the relationship between (129)I and( 137)Cs (corrected for background and decay from 1949 to 2005) accumulated levels, the background level of (129)I and the (129)I/(137)Cs ratio around Dolon were estimated to be (6.4 +/- 0.4) x 10(13) atoms m(-2) and 0.25 +/- 0.16, respectively. This (129)I/(137)Cs ratio is almost similar to the fission yield ratio for (239)Pu fast fission (0.24).

NQR and X-ray crystal structure studies of cadmium halide complexes: [C(NH{sub 2}){sub 3}]CdI{sub 3} and [4-ClC{sub 6}H{sub 5}NH{sub 3}]{sub 3}CdBr{sub 5}

Energy Technology Data Exchange (ETDEWEB)

Gesing, Thorsten M.; Lork, Enno [Bremen Univ. (Germany). MAPEX Center for Material and Processes; Terao, Hiromitsu [Tokushima Univ. (Japan). Faculty of Integrated Arts and Sciences; Ishihara, Hideta [Saga Univ. (Japan). Faculty of Culture and Education

2016-05-01

The crystal structures of [C(NH{sub 2}){sub 3}]CdI{sub 3} (1) and [4-ClC{sub 6}H{sub 5}NH{sub 3}]{sub 3}CdBr{sub 5} (2) have been determined at 100 K: monoclinic, Cc, a = 828.75(3) pm, b = 1615.31(5) pm, c = 810.64(3) pm, and β = 106.5820(10) for 1; monoclinic, P2{sub 1}/c, a = 1486.93(5) pm, b = 794.31(3) pm, c = 2290.59(7) pm, and β = 99.6830(10) for 2. The structure of 1 has an infinite chain of anions consisting of [CdI{sub 4}] tetrahedra sharing two corners. The structure of 2 has an infinite chain of anions consisting of [CdBr{sub 6}] octahedra sharing two corners in cis positions. In both structures, isolated cations are connected to the anion chains through weak hydrogen bonds Cd-X..H to result in three-dimensional network structures. In accordance with the crystal structures, three {sup 127}I (m = ±1/2 <-> m = ±3/2), five {sup 81}Br, and three {sup 35}Cl nuclear quadrupole resonance (NQR) lines were observed for 1 and 2. The NQR spectra reflect the anion chain structures and their weak hydrogen bonds. The MO calculations of the models [Cd{sub 5}I{sub 16}]{sup 6-} for 1 and [Cd{sub 3}Br{sub 16}]{sup 10-} for 2 estimate only about half the values for the NQR frequencies but give accurate electric field gradient directions.

Repeated Administration of D-Amphetamine Induces Distinct Alterations in Behavior and Metabolite Levels in 129Sv and Bl6 Mouse Strains

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Taavi Vanaveski

2018-06-01

Full Text Available The main goal of the study was to characterize the behavioral and metabolomic profiles of repeated administration (for 11 days of d-amphetamine (AMPH, 3 mg/kg i. p., indirect agonist of dopamine (DA, in widely used 129S6/SvEvTac (129Sv and C57BL/6NTac (Bl6 mouse strains. Acute administration of AMPH (acute AMPH induced significantly stronger motor stimulation in Bl6. However, repeated administration of AMPH (repeated AMPH caused stronger motor sensitization in 129Sv compared acute AMPH. Body weight of 129Sv was reduced after repeated saline and AMPH, whereas no change occurred in Bl6. In the metabolomic study, acute AMPH induced an elevation of isoleucine and leucine, branched chain amino acids (BCAA, whereas the level of hexoses was reduced in Bl6. Both BCAAs and hexoses remained on level of acute AMPH after repeated AMPH in Bl6. Three biogenic amines [asymmetric dimethylarginine (ADMA, alpha-aminoadipic acid (alpha-AAA, kynurenine] were significantly reduced after repeated AMPH. Acute AMPH caused in 129Sv a significant reduction of valine, lysophosphatidylcholines (lysoPC a C16:0, lysoPC a C18:2, lysoPC a C20:4, phosphatidylcholine (PC diacyls (PC aa C34:2, PC aa C36:2, PC aa C36:3, PC aa C36:4 and alkyl-acyls (PC ae C38:4, PC ae C40:4. However, repeated AMPH increased the levels of valine and isoleucine, long-chain acylcarnitines (C14, C14:1-OH, C16, C18:1, PC diacyls (PC aa C38:4, PC aa C38:6, PC aa C42:6, PC acyl-alkyls (PC ae C38:4, PC ae C40:4, PC ae C40:5, PC ae C40:6, PC ae C42:1, PC ae C42:3 and sphingolipids [SM(OHC22:1, SM C24:0] compared to acute AMPH in 129Sv. Hexoses and kynurenine were reduced after repeated AMPH compared to saline in 129Sv. The established changes probably reflect a shift in energy metabolism toward lipid molecules in 129Sv because of reduced level of hexoses. Pooled data from both strains showed that the elevation of isoleucine and leucine was a prominent biomarker of AMPH-induced behavioral sensitization