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Sample records for mediante 14c iii

  1. Study of the rearrangement of N-alkylanilines to P-aminoalkylbencene. III. N-n-propil-l-14{sup C} aniline; Estudio de la transposicion de N-Alquilanilinas a p-Aminoalquibenceno mediante 14{sup C}. III. N-n Propilanilina

    Energy Technology Data Exchange (ETDEWEB)

    Molera, J M; Gamboa, J M; Val del Cob, M; Ortin, N

    1964-07-01

    The rearrangement of N-n-propyl aniline to p-amino propylbenzene has been studied at 250 degree centigrade using several catalysts: CoCl{sub 2}, ZnCl{sub 2} and HBr. N-propyl-1-14{sup C}-aniline has been synthesized from sodium propionate-1-14{sup C} through conversion to n-propyl-1-14{sup C}-iodide and further reaction with aniline. After the rearrangement and among the reaction products both p-aminopropylbenzene and p-aminoisopropylbencene were found. To determine the 14{sup C} position in both the starting aniline and reaction products two degradation schemes are followed. In the light of experimental evidence a mechanism is set forth based on the assumption of an organic cation as intermediate. (Author) 13 refs.

  2. Myo-inositol-14C, phytic acid-14C and ferric phytate-14C metabolism through microbian action in an andosol soil

    International Nuclear Information System (INIS)

    Gonzalez I, J.

    1977-01-01

    The myo-inositol- 14 C, phytic acid- 14 C and ferric phytate- 14 C compounds were incubated in an andosol soil at 70% of the field capacity and at 36.5 deg C during twelve days. These compounds suffered a microbian oxidation at 14 CO 2 of 61.0, 1.9 and 0% respectively. The fixation of the phytic acid- 14 C was observed through the fast decrease in the metabolism, due to the formation of complexes with the Fe and Al (phytates). The myo-inositol- 14 C metabolism was reduced by a factor of nine at the second incubation day. The following mechanisms were observed in the myo-inositol metabolism: (i) adsorption of the inositol by the soil minerals, (ii) adsorption by humic acids, (iii) myo-inositol phosphorylation and (iv) epimerization of myo-inositol to chiro-inositol. It was found that the (i) and (ii) formation depends on the soil microbian activity. The (i), (ii) and (iii) interactions were considered as possible mechanisms for the inhibition of the myo-inositol microbian oxidation. The inhibition of the myo-inositol oxidation through adsorption or phosphorylation is considered as a chemical blockade for the hydroaxial group, avoiding this way a microbian oxidation stereospecific of this hydroxil group. (author)

  3. AMS-C14 analysis of graphite obtained with an Automated Graphitization Equipment (AGE III) from aerosol collected on quartz filters

    Energy Technology Data Exchange (ETDEWEB)

    Solís, C.; Chávez, E.; Ortiz, M.E.; Andrade, E. [Instituto de Física, Universidad Nacional Autónoma de México, 04510 México D.F. (Mexico); Ortíz, E. [Universidad Autónoma Metropolitana, Unidad Azcapotzalco, México D.F. (Mexico); Szidat, S. [Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern (Switzerland); Paul Scherrer Institut (PSI), CH-5232 Villigen (Switzerland); Wacker, L. [Laboratory of Ion Physics, ETH, Honggerberg, Zurich (Switzerland)

    2015-10-15

    AMS-{sup 14}C applications often require the analysis of small samples. Such is the case of atmospheric aerosols where frequently only a small amount of sample is available. The ion beam physics group at the ETH, Zurich, has designed an Automated Graphitization Equipment (AGE III) for routine graphite production for AMS analysis from organic samples of approximately 1 mg. In this study, we explore the potential use of the AGE III for graphitization of particulate carbon collected in quartz filters. In order to test the methodology, samples of reference materials and blanks with different sizes were prepared in the AGE III and the graphite was analyzed in a MICADAS AMS (ETH) system. The graphite samples prepared in the AGE III showed recovery yields higher than 80% and reproducible {sup 14}C values for masses ranging from 50 to 300 μg. Also, reproducible radiocarbon values were obtained for aerosol filters of small sizes that had been graphitized in the AGE III. As a study case, the tested methodology was applied to PM{sub 10} samples collected in two urban cities in Mexico in order to compare the source apportionment of biomass and fossil fuel combustion. The obtained {sup 14}C data showed that carbonaceous aerosols from Mexico City have much lower biogenic signature than the smaller city of Cuernavaca.

  4. Sex differences in HDL ApoC-III in American Indian youth

    Directory of Open Access Journals (Sweden)

    Blackett Piers R

    2012-08-01

    Full Text Available Abstract Background Since American Indians are predisposed to type 2 diabetes (DM2 and associated cardiovascular risk, Cherokee boys and girls (n = 917 were studied to determine whether BMI Z (body mass index Z score is associated with the apoC-III (apolipoprotein C-III content of HDL (high density lipoprotein, a previously reported predictor of DM2. Methods An ad hoc cross-sectional analysis was conducted on a previously studied cohort. Participants were grouped by gender-specific age groups (5 to 9, 10 to 14 and 15 to 19 years. ApoA-I (apolipoprotein A-I and HDL apoC-III were assayed by electroimmunoassay. ApoC-III was measured in whole plasma, and in HDL to determine the molar proportion to apoA-I. General linear models were used to assess association. Results The HDL apoC-III to apoA-I molar ratio increased by BMI Z quartile in girls aged 10–14 years (p  Conclusions ApoC-III showed an obesity-related increase relative to apoA-I during adolescence beginning in girls aged 10 to 14 years and in boys aged 15 to 19 years. The earlier changes in girls may alter HDL’s protective properties on the β-cell and contribute to their increased risk for DM2.

  5. Adsorption characteristics of 14C-labeled alanine, aspartic acid and adenosine triphosphate by metal-chelating resins

    International Nuclear Information System (INIS)

    Ishiyama, Toshio; Matsunami, Tadao; Shibata, Setsuko; Honda, Yoshihide.

    1987-01-01

    (1) Adsorption properties of 14 C-alanine, 14 C-ATP (adenosine triphosphate) and 14 C-aspartic acid on the metal-chelating resins were determined and found that the Cu(II)-Chelex 100 and Fe(III)-Unicellex UR10, Fe(III)-Chelex 100 chelating resins were highly effective for the adsorption of 14 C-alanine and 14 C-ATP, respectively. (2) Desorption rate of 14 C-ATP from the Fe(III)-Unicellex UR10 and Fe(III)-Chelex 100 resins was somewhat higher than the case of 14 C-alanine, probably because the coordination bonds of Cu-alanine might be stronger than those of Fe-ATP. Thus, 14 C-labeled organic compounds such as 14 C-alanine and 14 C-ATP of a low activity concentration (3.7 mBq/ml) (1 x 10 -7 μCi/ml) in aqueous solution may be measured with liquid scintillation counter after pre-concentration by use of the Fe(III)- and Cu(II)-chelating resin columns. (author)

  6. Comparación del gasto energético en reposo determinado mediante calorimetría indirecta y estimado mediante fórmulas predictivas en mujeres con grados de obesidad I a III

    OpenAIRE

    Alicia Parra-Carriedo; Loren Cherem-Cherem; Daniela Galindo-De Noriega; Mary Carmen Díaz-Gutiérrez; Ana Bertha Pérez-Lizaur; César Hernández-Guerrero

    2013-01-01

    Introducción: La determinación del gasto energético en reposo (GER) se calcula cotidianamente a partir de fórmulas predictivas aunque el resultado varía dependiendo de la población. Objetivo: Comparar la determinación del GER mediante calorimetría indirecta y mediante las ecuaciones Harris-Benedict (HB), Mifflin (MF), Organización Mundial de la Salud (OMS), "Institute of Medicine" (IOM), Fórmula Rápida (FR) y Valencia (VA) en mujeres con grados de obesidad I a III. Métodos: Mujeres adultas me...

  7. Behaviors of 14C-butachlor, 14C-chlorpyrifos and 14C-DDT in Rana japonica japonica Guenther

    International Nuclear Information System (INIS)

    Zhang Yiqiang; Zhong Chuangguang; Zhao Xiaokui; Chen Shunhua

    2002-01-01

    The research on the behaviors of 14 C-butachlor, 14 C-chlorpyrifos and 14 C-DDT in the frog Rana japonica japonica Guenther was carried out. After administrated per os to the frogs in doses of 380, 347, 363 Bq/g, 14 C-butachlor, 14 C-chlorpyrifos and 14 C-DDT, were distributed respectively to various organs within 24 h with specific accumulating organs as gallbladder, intestine and intestine, relevantly to the pesticides described. Compared to that in gallbladder and intestine, the radioactivity of many organs was extremely low, and this might due to the characters of the pesticides. Analysis of the metabolites of 14 C-DDT in frog at 24 th hr demonstrated that DDT was difficult to be degraded. Most 14 C-butachlor, 14 C-chlorpyrifos 14 C-DDT in liver and fat or ovary of frog was extractable with acetone. However, there were some differences between the pesticides, and the organs as well. And 14 C-butachlor, 14 C-chlorpyrifos or 14 C-DDT were better bound in liver than in fat

  8. Rapid radioimmunoassay of human apolipoproteins C-II and C-III

    Energy Technology Data Exchange (ETDEWEB)

    Gustafson, S; Oestlund-Lindqvist, A M; Vessby, B [Uppsala Univ. (Sweden)

    1984-06-01

    Apolipoprotein (apo) C-II is an activator of lipoprotein lipase, while apo C-III has the ability to inhibit apo C-II activated lipolysis. In order to study further the relationship between lipoprotein lipase mediated hydrolysis and the serum concentrations of apo C-II and apo C-III radioimmunoassays for these apolipoproteins have been developed. Formalin-treated Staphylococcus aureus Cowan I was used for immunoprecipitation and were shown to give rapid uptake of immune complexes that could easily be harvested by centrifugation. The assays were shown to be sensitive (10 ..mu..g/1), specific, precise (inter- and intra-assay coefficients of variation below 10%), rapid (completed in less than 6 h) and simple to perform. Delipidation of serum and lipoproteins had no effect on the results, indicating that the immunologically active sites of apo C-II and apo C-III are exposed to the aqueous environment under assay conditions. Serum apo C-II and apo C-III levels of normolipidaemic subjects were approximately 25 mg/1 and 110 mg/1, respectively. Highly significant positive correlations were found between VLDL apo C-II and VLDL apo C-III, respectively, and VLDL triglycerides, VLDL cholesterol and total serum TG. There was also a highly significant correlation between the HDL cholesterol concentration and the HDL apo C-III concentration.

  9. 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)

  10. Plasma apolipoprotein C-III levels, triglycerides, and coronary artery calcification in type 2 diabetics.

    Science.gov (United States)

    Qamar, Arman; Khetarpal, Sumeet A; Khera, Amit V; Qasim, Atif; Rader, Daniel J; Reilly, Muredach P

    2015-08-01

    Triglyceride-rich lipoproteins have emerged as causal risk factors for developing coronary heart disease independent of low-density lipoprotein cholesterol levels. Apolipoprotein C-III (ApoC-III) modulates triglyceride-rich lipoprotein metabolism through inhibition of lipoprotein lipase and hepatic uptake of triglyceride-rich lipoproteins. Mutations causing loss-of-function of ApoC-III lower triglycerides and reduce coronary heart disease risk, suggestive of a causal role for ApoC-III. Little data exist about the relationship of ApoC-III, triglycerides, and atherosclerosis in patients with type 2 diabetes mellitus (T2DM). Here, we examined the relationships between plasma ApoC-III, triglycerides, and coronary artery calcification in patients with T2DM. Plasma ApoC-III levels were measured in a cross-sectional study of 1422 subjects with T2DM but without clinically manifest coronary heart disease. ApoC-III levels were positively associated with total cholesterol (Spearman r=0.36), triglycerides (r=0.59), low-density lipoprotein cholesterol (r=0.16), fasting glucose (r=0.16), and glycosylated hemoglobin (r=0.12; Ptriglycerides (Tobit regression ratio, 1.43; 95% confidence interval, 0.94-2.18; P=0.086) and separately for very low-density lipoprotein cholesterol (Tobit regression ratio, 1.14; 95% confidence interval, 0.75-1.71; P=0.53). In persons with T2DM, increased plasma ApoC-III is associated with higher triglycerides, less favorable cardiometabolic phenotypes, and higher coronary artery calcification, a measure of subclinical atherosclerosis. Therapeutic inhibition of ApoC-III may thus be a novel strategy for reducing plasma triglyceride-rich lipoproteins and cardiovascular risk in T2DM. © 2015 American Heart Association, Inc.

  11. Ordered perovskites with cationic vacancies. 9. Compounds of the type Sr/sub 2/Srsub(1/4)Bsub(1/2)sup(III)vacantsub(1/4)WO/sub 6/ equivalent to Sr/sub 8/SrB/sub 2/sup(III)vacantW/sub 4/O/sub 24/ (Bsup(III) = La, Pr, Nd, Sm - Tm, Y)

    Energy Technology Data Exchange (ETDEWEB)

    Kemmler-Sack, S; Ehmann, A [Tuebingen Univ. (Germany, F.R.). Lehrstuhl fuer Anorganische Chemie 2

    1981-08-01

    The compounds Sr/sub 2/Srsub(1/4)Bsub(1/2)sup(III)vacantsub(1/4)WO/sub 6/ equivalent to Sr/sub 8/SrB/sub 2/sup(III)vacantW/sub 4/O/sub 24/ belong to the group of perovskites with octahedral cationic vacancies (cation/vacancy ratio (CN 6) = 7:1). For the larger Bsup(III) ions (La, Pr, Nd, Sm-Dy) different ordering effects are observed. The perovskites with Bsup(III) = Sm, Eu, Gd are polymorphic too (HT modification: higher ordered cubic perovskite (Bsup(III) = Gd: a = 2 x 8.23/sub 4/ A); LT modification: hexagonal perovskite stacking polytype (Bsup(III) = Gd: a = 9.95/sub 4/ A; c = 19.0/sub 4/ A)). With the smaller Bsup(III) ions (Ho, Er, Tm and Y) a cubic, 1:1 ordered perovskite type is observed.

  12. 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

  13. Bioconversion of α-[14C]Zearalenol and β-[14C]Zearalenol into [14C]Zearalenone by Fusarium roseum Gibbosum

    International Nuclear Information System (INIS)

    Richardson, K.E.; Hagler, W.M. Jr.; Hamilton, P.B.

    1984-01-01

    Cultures of Fusarium roseum Gibbosum on rice were treated with [ 14 C]zearalenone, α-[ 14 C]zearalenol, or β-[ 14 C]zearalenol to determine whether a precursor-product relationship exists among these closely related fungal metabolites. Culture extracts were purified by silica gel column chromatography and fractionated by high-pressure liquid chromatography, and the level of radioactivity was determined. Within 7 days, the β-[ 14 C]zearalenol was converted to zearalenone, and no residual β-[ 14 C]zearalenol was detectable. Most of the α-[ 14 C]zearalenol added was also converted into zearalenone within 14 days. In cultures treated with [ 14 C]zearalenone, no radioactivity was noted in any other components

  14. Formation of 14C-asparagine from 14C-precursor in mulberry leaves

    International Nuclear Information System (INIS)

    Yamashita, Tadaaki

    1981-01-01

    Since a remarkable accumulation of asparagine in the young leaves of mulberry has been observed, the formation of 14 C-asparagine from 14 C-labeled substrates in young leaves was examined in comparison with that in the mature leaves. 14 C-aspartic acid and 14 C-succinic acid expected as active precursors for asparagine biosynthesis, and 14 C-sucrose as respiratory substrates were fed respectively to the disks of young or mature leaves of mulberry. Although 14 C-succinic acid was actively converted to 14 C-asparagine, no significant amount of 14 C-asparagine was formed from 14 C-aspartic acid in two hours of feeding period. The rate of formation of 14 C-asparagine from 14 C-succinic acid in the mature leaves was slightly higher than that in the young leaves. Amino acids other than asparagine acquired 14 C from 14 C-labeled substrates were mainly aspartic acid, glutamic acid, alanine and ν-amino butyric acid in both of the leaves. Intending to accelerate the formation of asparagine in the leaves, ammonium ion was supplied to culturing solution as only source of nitrogen and plants were grown for two weeks in that solution before 14 C-labeled substrates feeding experiments. Supplying of ammonium ion brought about enhanced accumulation of asparagine in the young leaves, and caused remarkable formation of 14 C-asparagine from 14 C-aspartic acid in both of the leaves. However, the rate of 14 C-asparagine formation from 14 C-aspartic acid in the young leaves did not exceed that in the mature leaves. (author)

  15. NMR and TRLFS studies of Ln(iii) and An(iii) C5-BPP complexes.

    Science.gov (United States)

    Adam, Christian; Beele, Björn B; Geist, Andreas; Müllich, Udo; Kaden, Peter; Panak, Petra J

    2015-02-01

    C5-BPP is a highly efficient N-donor ligand for the separation of trivalent actinides, An(iii), from trivalent lanthanides, Ln(iii). The molecular origin of the selectivity of C5-BPP and many other N-donor ligands of the BTP-type is still not entirely understood. We present here the first NMR studies on C5-BPP Ln(iii) and An(iii) complexes. C5-BPP is synthesized with 10% 15 N labeling and characterized by NMR and LIFDI-MS methods. 15 N NMR spectroscopy gives a detailed insight into the bonding of C5-BPP with lanthanides and Am(iii) as a representative for trivalent actinide cations, revealing significant differences in 15 N chemical shift for coordinating nitrogen atoms compared to Ln(iii) complexes. The temperature dependence of NMR chemical shifts observed for the Am(iii) complex indicates a weak paramagnetism. This as well as the observed large chemical shift for coordinating nitrogen atoms show that metal-ligand bonding in Am(C5-BPP) 3 has a larger share of covalence than in lanthanide complexes, confirming earlier studies. The Am(C5-BPP) 3 NMR sample is furthermore spiked with Cm(iii) and characterized by time-resolved laser fluorescence spectroscopy (TRLFS), yielding important information on the speciation of trace amounts of minor complex species.

  16. Study of the reaction 14 C (p,p) 14 C

    International Nuclear Information System (INIS)

    Murillo, G.; Ramirez, J.; Avila, O.; Fernandez, M.; Darden, S.E.; Prior, R.P.; Sen, S.

    1991-04-01

    The study of the elastic scattering of polarized protons in 14 C, it has been very limited. Some angular distributions exists to low energy, as well as measures of excitation functions to several angles for the differential section and the vectorial analyzer power. A detailed study of the elastic scattering of protons by 14 C, it give us experimental information of the excited states in 15 N. The study of these states, is since of considerable interest it is not very easy to obtain a target of 14 C also in a reaction 14 C (p,p) 14 C is possible to obtain information of levels in 15 N to an excitation energy E X >14.95 MeV. (Author)

  17. Convenient synthesis of [2-14C]-methylglyoxal bis(guanylhydrazone), [14C]-mitoguazone

    International Nuclear Information System (INIS)

    Burgos, A.; Ellames, G.J.

    1995-01-01

    [2- 14 C]-Methylglyoxal bis(guanylhydrazone) dihydrochloride, [ 14 C]-mitoguazone has been prepared in three steps from potassium[1- 14 C]-acetate in an overall radiochemical yield of 16%. The key steps in this procedure are the formation of the sodium salt of[acetone-2- 14 C]-methylsulfinylacetone, and Pummerer rearrangement to the [ 14 C] labelled hermithioacetal, which is trapped with two equivalents of aminoguanidine to afford the desired [ 14 C]-mitoguazone. (Author)

  18. (C III lambda 1909/Si III lambda 1892) ratio as a diagnostic for planetary nebulae and symbiotic stars

    International Nuclear Information System (INIS)

    Feibelman, W.A.; Aller, L.H.; California Univ., Los Angeles)

    1987-01-01

    Suitable IUE archival material on planetary nebulae has been examined to determine the log R /F(lambda 1909 C III)/F(lambda 1892 Si III)/ as a discriminant for distinguishing planetary nebulae from symbiotic stars and related objects. The mean value of log R for 73 galactic planetaries is 1.4, while that of extragalactic planetaries appears to be slightly lower, and that for symbiotics is 0.3. The lower value of log R for symbiotics is easily understood as a consequence of their higher densities. A plot of log R versus N-epsilon indicates that 80 percent of the planetaries fall into the range of log R between 1.2 and 1.8, but some of the peculiar and bipolar nebulae fall below log R = 1.2. The corresponding N(C++)/N(Si++) ionic ratio varies over a large range. 53 references

  19. C III] EMISSION IN STAR-FORMING GALAXIES NEAR AND FAR

    Energy Technology Data Exchange (ETDEWEB)

    Rigby, J. R. [Astrophysics Science Division, Goddard Space Flight Center, 8800 Greenbelt Road, Greenbelt, MD 20771 (United States); Bayliss, M. B. [Department of Physics, Harvard University, 17 Oxford Street, Cambridge, MA 02138 (United States); Gladders, M. D. [Department of Astronomy and Astrophysics, University of Chicago, 5640 S. Ellis Avenue, Chicago, IL 60637 (United States); Sharon, K.; Johnson, T. [Department of Astronomy, University of Michigan, 500 Church Street, Ann Arbor, MI 48109 (United States); Wuyts, E. [Max Plank Institute for Extraterrestrial Physics, Giessenbachstrasse 1, D-85748 Garching (Germany); Dahle, H. [Institute of Theoretical Astrophysics, University of Oslo, P.O. Box 1029, Blindern, NO-0315 Oslo (Norway); Peña-Guerrero, M. [Space Telescope Science Institute, 3700 San Martin Drive, Baltimore, MD 21218 (United States)

    2015-11-20

    We measure [C iii] 1907, C iii] 1909 Å emission lines in 11 gravitationally lensed star-forming galaxies at z ∼ 1.6–3, finding much lower equivalent widths than previously reported for fainter lensed galaxies. While it is not yet clear what causes some galaxies to be strong C iii] emitters, C iii] emission is not a universal property of distant star-forming galaxies. We also examine C iii] emission in 46 star-forming galaxies in the local universe, using archival spectra from GHRS, FOS, and STIS on HST and IUE. Twenty percent of these local galaxies show strong C iii] emission, with equivalent widths < −5 Å. Three nearby galaxies show C iii] emission equivalent widths as large as the most extreme emitters yet observed in the distant universe; all three are Wolf–Rayet galaxies. At all redshifts, strong C iii] emission may pick out low-metallicity galaxies experiencing intense bursts of star formation. Such local C iii] emitters may shed light on the conditions of star formation in certain extreme high-redshift galaxies.

  20. Apolipoprotein C-II and C-III metabolism in a kindred of familial hypobetalipoproteinemia

    International Nuclear Information System (INIS)

    Malmendier, C.L.; Delcroix, C.; Lontie, J.F.; Dubois, D.Y.

    1991-01-01

    Three affected members of a kindred with asymptomatic hypobetalipoproteinemia (HBL) showed low levels of triglycerides, low-density lipoprotein (LDL)-cholesterol, and apolipoproteins (apo) B, C-II, and C-III. Turnover of iodine-labeled apo C-II and apo C-III associated in vitro to plasma lipoproteins was studied after intravenous injection. Radioactivity in plasma and lipoproteins (95% recovered in high-density lipoprotein [HDL] density range) and in 24-hour urine samples was observed for 16 days. A parallelism of the slowest slopes of plasma decay curves was observed between apo C-II and apo C-III, indicating a partial common catabolic route. Urine/plasma radioactivity ratio (U/P) varied with time, suggesting heterogeneity of metabolic pathways. A new compartmental model using the SAAM program was built, not only fitting simultaneously plasma and urine data, but also taking into account the partial common metabolism of lipoprotein particles (LP) containing apo C-II and apo C-III. The low apo C-II and C-III plasma concentrations observed in HBL compared with normal resulted from both an increased catabolism and a reduced synthesis, these changes being more marked for apo C-III. The modifications in the rate constants of the different pathways calculated from the new model are in favor of an increased direct removal of particles following the fast pathway, likely in the very-low-density lipoprotein (VLDL) density range

  1. Synthesis of carbon C-14 labelled 2-phenyl-4-alpha-alkylaminomethyl-quinolinemethanol: a potential anti-leishmaniasis agent

    Energy Technology Data Exchange (ETDEWEB)

    Wang, T.S.T.; Fawwaz, R.A.; Heertum, R.L.van [Columbia Univ., New York, NY (United States). Coll. of Physicians and Surgeons

    1995-07-01

    Using sodium acetate, [1-{sup 14}C] as a starting material, a total of seven steps were required to synthesize the title compound. This involved acylation of ortho-dichlorobenzene to form dichloroacetophenone, [2-{sup 14}C] (I). The 2-phenyl-4-quinoline carboxylic acid, [2-{sup 14}C] (II) was prepared by the Pfitzinger reaction from (1) and dichloroisatin. Compound 11 was converted to the acid chloride (III) by reaction with SOCl{sub 2} in benzene. Grignard condensation reaction of (III) yielded 4-quinolylmethylketone, [2-{sup 14}C] (IV) which was then converted to the bromomethylketone (V). Compound V was reacted with NaBH{sub 4} to form the ethylene oxide (VI). Alkylation of the oxide yielded the title compound (VII). The overall radiochemical yield was 10.1% and the specific activity was 3.0 mCi/mmol, with a radiochemical purity of >99.5%. (author).

  2. Study of the rearrangement of N-alkylaniline to p-aminoalkylbencene. I. N-ethyl-l-{sup 1}4C-aniline; Estudio de la transposicion de N-alquilanilinas A p-Aminoalquilbenceno mediante {sup 1}4C

    Energy Technology Data Exchange (ETDEWEB)

    Molera, M J; Gamboa, J M; Val Cob, M del

    1961-07-01

    The rearrangement of N-ethylaniline to p-aminoethylbenzene has been studied over the temperature range 200-300 degree centigrade using different catalysts: Cl{sub 2}Co, Cl{sub 2}Zn, Cl{sub 2}Ni, Cl{sub 3}Al, Cl{sub 2}Cd and Br H.N-ethyl-1-{sup 1}4C-aniline has been synthesized from ethyl-1-{sup 1}4C-iodide and aniline and its rearrangement to p-aminoethyl-benzene proves that the ethyl group does not rearrange itself during the reaction. A scheme for the degradation of both the N-ethyl-1-{sup 1}4C aniline and the p-aminoethylbenzene produces is described. (Author) 14 refs.

  3. Desarrollo de la tecnología de MOVPE para el crecimiento de semiconductores III-V : fabricación de células solares para concentraciones luminosas elevadas

    OpenAIRE

    Galiana Blanco, Beatriz

    2011-01-01

    El trabajo de estas tesis trata sobre el desarrollo en el IES-UPM de la tecnología de crecimiento epitaxial de fase vapor mediante precursores metalorgánicos (MOVPE) para el crecimiento de células solares de semiconductores III-V para concentraciones luminosas elevadas. En la primera parte de la memoria se presentan los principios de la MOVPE y el estudio de los materiales semiconductores utilizados a lo largo de la tesis: GaAs, AlGaAs, GaInP y AlInP. Para ello, se ha analizado cómo influ...

  4. A convenient photosynthesis of uniformly [14C]-labelled D-glucose, D-fructose and sucrose, and chemical synthesis of methyl-α-D-glucopyranoside ([U-14C]-glucose)

    International Nuclear Information System (INIS)

    Srinivas, G.; Unny, V.K.P.; Mukkanti, K.; Choudary, B.M.

    2013-01-01

    This paper describes a convenient procedure for the radiochemical preparation of D-[U- 14 C]-glucose, D-[U- 14 C]-fructose and [U- 14 C]-sucrose with high specific activity by photosynthesis using ‘canna indica’ leaf, [ 14 C]-carbon dioxide and water in presence of light in a closed system. The [ 14 C]-sugars formed were extracted, separated and then purified by paper chromatography. Further, the pure D-[U- 14 C]-glucose obtained was converted to methyl-α-D-glucopyranoside ([U- 14 C]-glucose) by glycosidation with methanol using (i) HCl, the conventional Fischer method (ii) heterogeneous organic cation exchange resin (Amberlite IR-120 (H + )) and (iii) heterogeneous inorganic cation exchanged montmorillonites called metal M +n -monts. The results indicated that the latter in the form of Fe +3 -montmorillonite gave a better yield ( 65%) as compared to others (40–56%). The radiochemical purity of the no-carrier added product was more than 98%. The product retained its specific activity as that of the starting material which is in the range of 250–300 mCi/mmole (9.25–11.1 GBq/mmole), suitable for use as a radiotracer in biochemical investigations. - Graphical abstract: A convenient photosynthesis of uniformly [ 14 C]-labelled D-glucose, D-fructose and sucrose, and chemical synthesis of methyl-α-D-glucopyranoside ([U- 14 C]-glucose)/[ 14 C]–AMG, in short. The photosynthesis of D-[U- 14 C]-glucose, and two other [ 14 C]-sugars (fructose and sucrose) with high specific activity using ‘Canna indica’ leaf, 14 CO 2 and water in presence of light is presented in this paper. Further, the D-[U- 14 C]-glucose obtained was converted to methyl-α-D-glucopyranoside ([U- 14 C]-glucose)/[ 14 C]–AMG having 98% radiochemical purity and specific activity in the range of 250–300 mCi/mmole, using montmorillonites (M +n -monts). Highlights: ► Synthesis of methyl α D-glucopyranoside ([U- 14 C] glucose) has not been reported using M +n -monts. ► M +n -monts are

  5. A convenient synthesis of sup 14 C-cotinine from sup 14 C-nicotine

    Energy Technology Data Exchange (ETDEWEB)

    Desai, D.H.; Djordjevic, M.V.; Amin, S. (American Health Foundation, Valhalla, NY (USA). Naylor Dana Inst. for Disease Prevention)

    1991-03-01

    A convenient synthesis with analytical monitoring of {sup 14}C-cotinine is reported. {sup 14}C-Nicotine was converted into {sup 14}C-dibromocotinine hydrobromide perbromide. Debromination, achieved by using Zn dust/acetic acid, resulted in high yields (71%) of {sup 14}C-cotinine. (author).

  6. Syntheses of [6-14C] and [5-carboxy, 6-14C2]nitrendipine

    International Nuclear Information System (INIS)

    Maul, N.; Scherling, D.

    1989-01-01

    [6- 14 C]Nitrendipine synthesis started from barium[ 14 ]carbonate, which was converted to [1- 14 C]acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl [3- 14 C]acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino[3- 14 C]crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain [6- 14 C]nitrendipine. (author)

  7. 14N NMR of amminecobalt(III) compounds

    DEFF Research Database (Denmark)

    Kofod, Pauli

    2003-01-01

    Directly detected ammine 14N NMR chemical shifts of 20 amminecobalt(III) compounds are reported. The coordination shifts, δCS = δcoord − δfree, are in all cases negative and range from −4.4 ppm for the trans ammine ligand in [Co(NH3)5(CH3)]2+ to −73.6 ppm for the trans ammine ligand in [Co(NH3)5(F...

  8. Convenient synthesis of [2-{sup 14}C]-methylglyoxal bis(guanylhydrazone), [{sup 14}C]-mitoguazone

    Energy Technology Data Exchange (ETDEWEB)

    Burgos, A.; Ellames, G.J. [Sterling Winthrop Research Centre, Alnwick (United Kingdom). Pharmaceuticals Research Div.

    1995-01-01

    [2-{sup 14}C]-Methylglyoxal bis(guanylhydrazone) dihydrochloride, [{sup 14}C]-mitoguazone has been prepared in three steps from potassium[1-{sup 14}C]-acetate in an overall radiochemical yield of 16%. The key steps in this procedure are the formation of the sodium salt of[acetone-2-{sup 14}C]-methylsulfinylacetone, and Pummerer rearrangement to the [{sup 14}C] labelled hermithioacetal, which is trapped with two equivalents of aminoguanidine to afford the desired [{sup 14}C]-mitoguazone. (Author).

  9. Synthesis and in vitro cytotoxicity of novel C-12 substituted-14-deoxy-andrographolide derivatives as potent anti-cancer agents.

    Science.gov (United States)

    Kandanur, Sai Giridhar Sarma; Golakoti, Nageswara Rao; Nanduri, Srinivas

    2015-12-15

    Andrographolide, the major labdane diterpenoid from Andrographis paniculata has been reported to be cytotoxic against various cancer cells in vitro. Our research efforts led to the discovery of novel 12-phenyl thio and 12-aryl amino-14-deoxy-andrographolide derivatives (III q and III r) with potent cytotoxic activity, 12-benzyl amino-14-deoxy-andrographolide analogues showing broad range of cytotoxic activity against most of the cell lines and 12-alkyl amino-14-deoxy-andrographolide derivatives being selective to few cell lines (PC-3 and HOP-92), when the selected analogues were evaluated against 60 human cancer cell line panel at National Cancer Institute (N.C.I.), USA. The SAR (structure activity relationship) studies demonstrated potent activity for the compounds containing the following functionalities at C-12: substituted aryl amino/phenyl thio>benzylamine>alkyl amine. The significant cytotoxic activity observed for compounds III q and III r suggest that these could serve as templates for further optimization. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. 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)

  11. Synthesis of [21-14C]-fusarin C by enzymic demethylation and remethylation with [14C]-diazomethane

    International Nuclear Information System (INIS)

    Lu, S.-J.; Li, M.H.

    1989-01-01

    Fusarin C, a potent mutagen isolated from Fusarium moniliforme culture extracts, has been prepared radiolabeled in two steps by enzymic hydrolysis of the 21-methyl ester group, using phenobarbital induced microsomal preparations, followed by remethylation using [ 14 F]-diazomethane. Yields, based upon fusarin C, were essentially quantitative and approximately 10% of the [ 14 C]-methyl-nitrosourea, converted to diazomethane, reacted to yield [ 14 C]-fusarin C. (author)

  12. Study of the rearrangement of N-alkylanilines to P-aminoalkylbencene. III. N-n-propil-l-14C aniline

    International Nuclear Information System (INIS)

    Molera, J. M.; Gamboa, J. M.; Val del Cob, M.; Ortin, N.

    1964-01-01

    The rearrangement of N-n-propyl aniline to p-amino propylbenzene has been studied at 250 degree centigrade using several catalysts: CoCl 2 , ZnCl 2 and HBr. N-propyl-1-14 C -aniline has been synthesized from sodium propionate-1-14 C through conversion to n-propyl-1-14 C -iodide and further reaction with aniline. After the rearrangement and among the reaction products both p-aminopropylbenzene and p-aminoisopropylbencene were found. To determine the 14 C position in both the starting aniline and reaction products two degradation schemes are followed. In the light of experimental evidence a mechanism is set forth based on the assumption of an organic cation as intermediate. (Author) 13 refs

  13. Reconstrucción funcional de brazo en fractura abierta III C de húmero

    Directory of Open Access Journals (Sweden)

    M. Mendieta-Espinosa

    2014-09-01

    Full Text Available Las fracturas abiertas de alta energía tipo III C de Gustilo requieren un abordaje multidisciplinario en el que intervendrán distintas especialidades médicas, personal paramédico y demás profesionales de la salud, a fin de lograr una adecuada evolución del paciente y la restauración de su extremidad. La selección del procedimiento reconstructivo de cobertura dependerá de la localización y magnitud del defecto; pero se necesita una adecuada coordinación para llevar a cabo de forma oportuna la revascularización, la estabilización ósea y la cobertura de tejidos blandos que son la base de un procedimiento exitoso que prevenga la infección, favorezca la consolidación de la fractura y proteja las estructuras óseas, cartilaginosas, tendinosas y neurovasculares. Presentamos el caso de un paciente varón de 20 años de edad con fractura abierta de húmero III C según la clasificación de Gustilo, tratado con revascularización mediante colocación de injertos de vena safena a vasos braquiales, y secuencialmente, fijación intramedular de húmero y cobertura con colgajo músculo-cutáneo de dorsal ancho. Tras 10 días de estancia hospitalaria, el paciente logró una adecuada cobertura de la zona de la fractura abierta y restablecimiento de la función de flexión del codo.

  14. Uptake and distribution of 14C during and following exposure to [14C]methyl isocyanate

    International Nuclear Information System (INIS)

    Ferguson, J.S.; Kennedy, A.L.; Stock, M.F.; Brown, W.E.; Alarie, Y.

    1988-01-01

    Guinea pigs were exposed to [ 14 C]methyl isocyanate ( 14 CH 3 -NCO, 14 C MIC) for periods of 1 to 6 hr at concentrations of 0.5 to 15 ppm. Arterial blood samples taken during exposure revealed immediate and rapid uptake of 14 C. Clearance of 14 C was then gradual over a period of 3 days. Similarly 14 C was present in urine and bile immediately following exposure, and clearance paralleled that observed in blood. Guinea pigs fitted with a tracheal cannula and exposed while under anesthesia showed a reduced 14 C uptake in blood indicating that most of the 14 C MIC uptake in normal guinea pigs occurred from retention of this agent in the upper respiratory tract passages. In exposed guinea pigs 14 C was distributed to all examined tissues. In pregnant female mice similarly exposed to 14 C MIC, 14 C was observed in all tissues examined following exposure including the uterus, placenta, and fetus. While the form of 14 C distributed in blood and tissues has not yet been identified, these findings may help to explain the toxicity of MIC or MIC reaction products on organs other than the respiratory tract, as noted by several investigators

  15. Triglyceride-rich lipoprotein metabolism in women: roles of apoC-II and apoC-III.

    Science.gov (United States)

    Ooi, Esther M; Chan, Dick C; Hodson, Leanne; Adiels, Martin; Boren, Jan; Karpe, Fredrik; Fielding, Barbara A; Watts, Gerald F; Barrett, P Hugh R

    2016-08-01

    Experimental data suggest that apolipoprotein (apo) C-II and C-III regulate triglyceride-rich lipoprotein (TRL) metabolism, but there are limited studies in humans. We investigated the metabolic associations of TRLs with apoC-II and apoC-III concentrations and kinetics in women. The kinetics of plasma apoC-II, apoC-III and very low-density lipoprotein (VLDL) apoB-100 and triglycerides were measured in the postabsorptive state using stable isotopic techniques and compartmental modelling in 60 women with wide-ranging body mass index (19·5-32·9 kg/m(2) ). Plasma apoC-II and apoC-III concentrations were positively associated with the concentrations of plasma triglycerides, VLDL1 - and VLDL2 -apoB-100 and triglyceride (all P triglyceride concentration and VLDL1 triglyceride PR, while apoC-II fractional catabolic rate (FCR) was positively associated with VLDL1 triglyceride FCR (all P triglyceride kinetics. ApoC-III PR, but not FCR, was positively associated with VLDL1 triglyceride, and VLDL2 -apoB-100 and triglyceride concentrations (all P triglyceride kinetics. In multivariable analysis, including homoeostasis model assessment score, menopausal status and obesity, apoC-II concentration was significantly associated with plasma triglyceride, VLDL1 -apoB-100 and VLDL1 triglyceride concentrations and PR. Using the same multivariable analysis, apoC-III was significantly associated with plasma triglyceride and VLDL1 - and VLDL2 -apoB-100 and triglyceride concentrations and FCR. In women, plasma apoC-II and apoC-III concentrations are regulated by their respective PR and are significant, independent determinants of the kinetics and plasma concentrations of TRLs. © 2016 Stichting European Society for Clinical Investigation Journal Foundation.

  16. Synthesis of [2-13C, 2-14C] 2-aminoethanol, [1-13C, 1-14C] 2-chloroethylamine, N,N'-bis([1-13C, 1-14C] 2-chloroethyl)-N-nitrosourea(BCNU) and N-([1-13C, 1-14C] 2-chloroethyl)-N-nitrosourea(CNU)

    International Nuclear Information System (INIS)

    Narayan, R.; Chang, C-j.

    1982-01-01

    [2- 13 C, 2- 14 C]2-Aminoethanol hydrochloride was prepared in good yield from Na*CN in a two step sequence by first converting the Na*CN to OHCH 2 *CN and then reducing the nitrile directly with a solution of borane-tetrahydrofuran complex. The reaction procedure was simple and the pure product could be obtained readily. Using this specifically labelled precursor, the synthesis of [1- 13 C, 1- 14 C]2-chloroethylamine hydrochloride, N-([1- 13 C, 1- 14 C]2-chloroethyl)-N-nitrosourea(CNU) and N,N'-bis([1- 13 C, 1- 14 C]2-chloroethyl)-N-nitrosourea(BCNU) in good yield without isotope scrambling was also reported. (author)

  17. Crystal structure of fac-[2-(4-methyl-5-phenylpyridin-2-ylphenyl-κ2C1,N]bis[2-(pyridin-2-ylphenyl-κ2C1,N]iridium(III

    Directory of Open Access Journals (Sweden)

    Chi-Heon Lee

    2016-12-01

    Full Text Available In the title compound, [Ir(C11H8N2(C18H14N], the IrIII ion adopts a distorted octahedral coordination environment defined by three C,N-chelating ligands, one stemming from a 2-(4-phenyl-5-methylpyridin-2-ylphenyl ligand and two from 2-(pyridin-2-ylphenyl ligands, arranged in a facial manner. The IrIII ion lies almost in the equatorial plane [deviation = 0.0069 (15 Å]. In the crystal, intermolecular π–π stacking interactions, as well as intermolecular C—H...π interactions, are present, leading to a three-dimensional network.

  18. Rhodium(III)- and iridium(III)-catalyzed C7 alkylation of indolines with diazo compounds.

    Science.gov (United States)

    Ai, Wen; Yang, Xueyan; Wu, Yunxiang; Wang, Xuan; Li, Yuanchao; Yang, Yaxi; Zhou, Bing

    2014-12-22

    A Rh(III)-catalyzed procedure for the C7-selective C-H alkylation of various indolines with α-diazo compounds at room temperature is reported. The advantages of this process are: 1) simple, mild, and pH-neutral reaction conditions, 2) broad substrate scope, 3) complete regioselectivity, 4) no need for an external oxidant, and 5) N2 as the sole byproduct. Furthermore, alkylation and bis-alkylation of carbazoles at the C1 and C8 positions have also been developed. More significantly, for the first time, a successful Ir(III)-catalyzed intermolecular insertion of arene C-H bonds into α-diazo compounds is reported. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. A procedure for batch separation of 14C-hexose from 14C-sucrose

    International Nuclear Information System (INIS)

    Tarpley, L.; Vietor, D.M.

    1991-01-01

    This presentation describes a method for separating 14 C-hexose from 14 C-sucrose in extracts of plant tissue. Portions of ethanol extracts are treated with activated charcoal in microcentrifuge tubes. Aliquots are removed, ethanol evaporated and replaced with reaction mixture that phosphorylates hexose (HEPPS, K 2 HPO 4 , Mg(C 2 H 3 O 2 ) 2 , ovalbumen, Na 2 ATP, yeast hexokinase). After a time course, the hexokinase reaction is stopped (slowed considerably) to minimize effects of contamination enzyme activities. The stopping agent used is lyxose, a nonphosphorylable analogue of glucose. The strong anionic charge of phosphate introduced through the hexokinase action results in binding (> 95%) of hexose-phosphate to anion-exchange resin. Sucrose remains unbound (> 95%) in solution. This batch ion-exchange is performed in microcentrifuge tubes to allow many samples to be processed simultaneously. Recovery of radiolabel in extracts is complete (99%), and determinations are repeatable (cv = 23%). This method for routinely separating and quantifying 14 C-hexose and 14 C-sucrose in plant tissue extracts can contribute to the economy and feasibility of studies of 14 C-photoassimilate partitioning to soluble sugars within and among plant tissues

  20. Syntheses of (6- sup 14 C) and (5-carboxy, 6- sup 14 C sub 2 )nitrendipine

    Energy Technology Data Exchange (ETDEWEB)

    Maul, N.; Scherling, D. (Bayer AG, Wuppertal (Germany, F.R.). Inst. fuer Pharmakologie)

    1989-04-01

    (6-{sup 14}C)Nitrendipine synthesis started from barium({sup 14})carbonate, which was converted to (1-{sup 14}C)acetyl chloride. The acid chloride was condensed with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione). The resulting intermediate was treated with boiling methanol to give methyl (3-{sup 14}C)acetoacetate. The reaction with gaseous ammonia in toluene yielded the corresponding methyl 3-amino(3-{sup 14}C)crotonate which was condensed with ethyl 2-(3-nitro-benzylidene) acetoacetate to obtain (6-{sup 14}C)nitrendipine. (author).

  1. Synthesis and biological evaluation of new C-12(α/β)-(N-) sulfamoyl-phenylamino-14-deoxy-andrographolide derivatives as potent anti-cancer agents.

    Science.gov (United States)

    Kandanur, Sai Giridhar Sarma; Nanduri, Srinivas; Golakoti, Nageswara Rao

    2017-07-01

    Andrographolide, the major diterpenoidal constituent of Andrographis paniculata (Acanthaceae) and its derivatives have been reported to possess plethora of biological properties including potent anti-cancer activity. In this work, synthesis and in-vitro anti-cancer evaluation of new C-12-substituted aryl amino 14-deoxy-andrographolide derivatives (III a-f) are reported. The substitutions include various sulfonamide moieties -SO 2 -NH-R 1 . The new derivatives (III a-e) exhibited improved cytotoxicity (GI 50 , TGI and LC 50 ) compared to andrographolide (I) and the corresponding 3,14,19-O-triacetyl andrographolide (II) when evaluated against 60 NCI cell line panel. Compounds III c and III e are found to be non-toxic to normal human dermal fibroblasts (NHDF) cells compared to reference drug THZ-1. Copyright © 2017 Elsevier Ltd. All rights reserved.

  2. Apolipoproteins C-II and C-III as nutritional markers unaffected by inflammation.

    Science.gov (United States)

    Isshiki, Miwa; Hirayama, Satoshi; Ueno, Tsuyoshi; Ito, Masayuki; Furuta, Ayaka; Yano, Kouji; Yamatani, Kotoko; Sugihara, Masami; Idei, Mayumi; Miida, Takashi

    2018-06-01

    Rapid turnover proteins (RTPs), such as transthyretin (TTR), retinol binding protein (RBP), and transferrin (Tf), provide an accurate assessment of nutritional status but are susceptible to inflammation. Lipid-related markers, which have short half-lives in serum, may be better suited for nutritional assessment. We sought to identify sensitive nutritional markers unaffected by inflammation. Fasting serum samples were collected from 30 malnourished inpatients and 25 healthy volunteers. Malnourished inpatients were divided into 2 groups: a low-C-reactive protein (CRP) group (CRP group (CRP ≥ 20 mg/l, n = 15). Lipid-related markers, traditional nutritional markers, RTPs, micronutrients, and ketone bodies were measured and compared among the groups. Apolipoprotein (Apo)C-II and ApoC-III concentrations were lower in malnourished inpatients than in the control group. There was no significant difference in ApoC-II and ApoC-III between the low- and high-CRP groups. Carnitine transporters and ketone bodies did not show a significant difference among the three groups. Albumin, TTR, RBP, and Tf concentrations were lowest in the high-CRP group, intermediate in the low-CRP group, and highest in the control group. These results indicate that ApoC-II and ApoC-III are appropriate nutritional biomarkers unaffected by inflammation. Copyright © 2018 Elsevier B.V. All rights reserved.

  3. 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.)

  4. Synthesis of 14C analogue of 1,2-diaryl-[2-14C]-pyrroles

    International Nuclear Information System (INIS)

    Saemian, N.; Shirvani, G.; Matloubi, H.

    2007-01-01

    Three 1,2-diaryl pyrroles selective COX-2 inhibitors, 2-(4-fluorophenyl)-5-methyl-1-(4-methylsulfonyl-phenyl)-1H pyrrole, 2-(4-fluorophenyl)-1- [4-(methylsulfonyl) phenyl]-1H-pyrrole and 4-[2-(4-fluorophenyl)-1H-pyrrol-1-yl]benzenesulfon-amide, all three labeled with 14 C in the 2-position were prepared from para-fluoro-benzaldehyde-[carbonyl- 14 C]. (author)

  5. Synthesis of pinacolyl [14C]methylphosphonochloridate

    International Nuclear Information System (INIS)

    Horvat, J.; Keglevic, D.; Klaic, B.; Kveder, S.; Ladesic, B.; Cosic, M.; Zupanc, S.

    1982-01-01

    A three-step synthetic route to pinacolyl [ 14 C]methylphosphonochloridate (3) from [ 14 C]methyl iodide is described. Condensation of sodium di-n-butyl phosphite with [ 14 C]methyl iodide gave di-n-butyl [ 14 C]methylphosphonate (1) which was converted into [ 14 C]methylphosphonic dichloride (2) by prolonged refluxing with thionyl chloride. Reaction of 2 with pinacolyl alcohol in the presence of N,N-di-n--propylaniline as the base afforded the title compound 3. The radiochemical yield of redistilled 3 was 34,2% based on 1, and the overall radiochemical yield was 20,0% from [ 14 C]methyl iodide. (author)

  6. Preparation of D-[U-14C]galactose and α-D-[U-14C]galactose-1-phosphate

    International Nuclear Information System (INIS)

    Kolina, J.; Hromadkova, B.

    1989-01-01

    Optically pure D-[U- 14 C]galactose was prepared on a preparatory scale using the galactokinase enzyme. The suggested procedure allows to also prepare a α-D-[U- 14 C]galactose-1-phosphate and L-[U- 14 ]galactose giving good yield. The experiments proved that the raw fraction isolated from yeast of the Kluyveromyces fragilis strain or the Kluyveromyces lactis strain shows sufficient activity. Phosphorylation of D-[U- 14 C]galactose practically terminates after 30 mins of incubation. DL-[U- 14 C]galactose isolated using preparatory paper chromatography from the acid hydrolyzate of [U- 14 C] polysaccharide is a satisfactory radioactive precursor. The developed preparation procedure theoretically contributed towards the further elucidation of the problem of the proportional representation of galactose stereo-isomers in extracellular polysaccharide isolated from red algae. In this respect data in the literature differ and some sources state a significantly higher propertion of L-galactose. The experiments showed that [U- 14 C] polysaccharide isolated from the red algae Porphyridium cruentum prevalently contains D-[U- 14 C]galactose, which confirms the process of enzyme reaction. (author). 1 tab., 4 refs

  7. Root-uptake of 14C derived from acetic acid and 14C transfer to rice edible parts

    International Nuclear Information System (INIS)

    Ogiyama, Shinichi; Suzuki, Hiroyuki; Inubushi, Kazuyuki; Takeda, Hiroshi; Uchida, Shigeo

    2010-01-01

    Three types of culture experiments using paddy rice (Oryza sativa L.) were performed to examine root-uptake of 14 C in the form of acetic acid: double pot experiment (hydroponics), wet culture experiment (submerged sand medium), and chamber experiment (hydroponics and submerged sand medium). The 14 C radioactivity in the plant, mediums, and atmospheric carbon dioxide ( 14 CO 2 ) in the chamber were determined, and the distribution of 14 C in the plant was visualized using autoradiography. In the double pot experiment, the shoot of the plant and the lower root which was soaked in the culture solution had 14 C radioactivity, but the upper root which did not have contact with the solution had none. There were also 14 C radioactivity in the grains and roots in the wet culture experiment. Results of the chamber experiment showed that 14 CO 2 gas was released from the culture solution in both types of cultures. Results indicated that the 14 C-acetic acid absorbed by rice plant through its root would be very small. Most of the 14 C-acetic acid was transformed into gaseous forms either in the culture solution or rhizosphere. A relatively longer time would be needed to assimilate 14 C derived from acetic acid to grain parts after it was once absorbed by the shoot through the root. Availability of 14 C for the plant in sand culture was considered to be decreased compared with that for the plant in the hydroponics experiment. It was suggested that rice plant absorbed and assimilated 14 C through the plant roots not because of uptake of 14 C-acetic acid but because of uptake of 14 C in gaseous forms such as 14 CO 2 .

  8. 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

  9. Determination of stability constants for thallium(III) cyanide complexes in aqueous solution by means of 13C and 205Ti NMR

    International Nuclear Information System (INIS)

    Blixt, J.; Gyori, B.; Glaser, J.

    1989-01-01

    In contrast to what is usually assumed, we have found and proved that thallium(III) forms very strong cyanide complexes in aqueous solution. The authors have investigated this system using 205 Tl, 13 C, and 14 N NMR and potentiometry and established the existence of four thallium(III)-cyanide complexes of the composition Tl(CN) n 3-n , n = 1-4. We have measured their chemical shifts and spin-spin coupling constants and determined their formation constants at 25 degree C in dilute (0.05 M) aqueous solution in the ionic medium ([Na + ] = 1 M, [Li + ] + [H + ] = 3 M, [ClO 4 - ] = 4 M). We have also determined the stability constant for HCN in the same ionic medium, log K a = 10.11 (5)

  10. Synthesis of disodium [benzene-U-{sup 14}C]-(4-chlorophenylthio)methylenediphosphonate, [benzene-U-{sup 14}C]-tiludronate

    Energy Technology Data Exchange (ETDEWEB)

    Burgos, Alain; Ellames, G.J. [Alnwick Research Centre (United Kingdom). Dept. of Metabolism and Pharmacokinetics

    1995-12-31

    Disodium [benzene-U-{sup 14}C]-(4-chlorophenylithio)methylenediphosphonate, [benzene-{sup 14}C]-Tiludronate, 2, has been prepared in six steps from [benzene-U-{sup 14}C]-acetanilide in an overall radiochemical yield of 41%. A key step in this transformation was the efficient conversion of [U-{sup 14}C]-4-chloroaniline to [benzene-U-{sup 14}C]-4-chlorophenylthiocyanate, 5, in 83% yield by treatment of the corresponding diazonium salt, 9 with iron(111) thiocyanate. It should be noted that formation of the isomeric [benzene-U-{sup 14}C]-4-chlorophenylisothiocyanate, 11, as a byproduct, was observed in only {approx} 1% yield. (author).

  11. Synthesis of cholesterol 26. C{sup 14} (1961); Synthese du cholesterol {sup 14}C-26 (1961)

    Energy Technology Data Exchange (ETDEWEB)

    Herbert, M; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    Cholesterol 26 {sup 14}C is synthesized from methylmagnesium iodide {sup 14}C with a 48 per cent overall yield. Cholesterol is purified by chromatography on alumina. The various intermediates of the synthesis are characterized by thin-layer chromatography according to Stahl. (authors) [French] Le cholesterol {sup 14}C-26 est synthetise a partir d'iodure de methyl magnesium {sup 14}C, avec un rendement de 48 pour cent par rapport a l'iodure de methyl {sup 14}C mis en jeu. Le cholesterol est purifie par chromatographie sur alumine. Les intermediaires de la synthese sont caracterises par chromatographie en couche mince, selon Stahl. (auteurs)

  12. Synthesis of [methyl-14C]crotonobetaine from DL-[methyl-14C]carnitine

    International Nuclear Information System (INIS)

    Loester, H.; Seim, H.

    1996-01-01

    The causes of carnitine deficiency syndromes are not completely understood, but decomposition of L-carnitine in vivo is likely to be involved. Carnitine is metabolized to γ-butyrobetaine, and crotonobetaine is probably an intermediate in this pathway. To validate experimentally the precursor-product relationship between the three physiologically occuring γ-betaines - L-carnitine, crotonobetaine, γ-butyrobetaine - labelling with stable or radioactive isotopes became necessary. Methyl-labelled carnitine isomers (L(-)-, D(+)- or DL-) or γ-butyrobetaine can be easily synthesized by methylation of 4-amino-3-hydroxybutyric acid isomers or 4-aminobutyric acid, respectively. Because of problems with the 4-aminocrotonic acid, we synthesized labelled crotonbetaine from labelled carnitine. Thus, DL-[methyl- 14 C]carnitine was dehydrated by reaction with concentrated sulfuric acid. After removal of the latter the products were separated and purified by ion exchange chromatography on DOWEX 50 WX8 (200 - 400 mesh) and gradient elution with hydrochloric acid. In addition to the labelled main product [methyl- 14 C]crotonobetaine (yield about 50 %), [methyl- 14 C]glycine betaine and [methyl- 14 C]acetonyl-trimethylammonium (ATMA) were formed. The end products were identified by combined thin layer chromatography/autoradiography and quantified by liquid scintillation counting. (Author)

  13. Synthesis of 14C-dehydrocorydaline chloride

    International Nuclear Information System (INIS)

    Zhang Rui; Wang Ding

    1988-01-01

    A method for synthesis of 14 C-dehydrocorydaline chloride is described. In the presence of sodium hydroxide, acetonylpalmatine is reacted with 14 C-methyl iodide in sealed glass ampoule to give 14 C-13-methylpalmatine iodide which is then converted to chloride. The radiochemical purity of 14 C-dehydrocorydaline determined by TLC is over 98% and the labelling efficiency is 54%

  14. PHOTOIONIZATION MODELS FOR THE SEMI-FORBIDDEN C iii] 1909 EMISSION IN STAR-FORMING GALAXIES

    Energy Technology Data Exchange (ETDEWEB)

    Jaskot, A. E. [Department of Astronomy, Smith College, Northampton, MA 01063 (United States); Ravindranath, S. [Space Telescope Science Institute, Baltimore, MD 21218 (United States)

    2016-12-20

    The increasing neutrality of the intergalactic medium at z  > 6 suppresses Ly α emission, and spectroscopic confirmation of galaxy redshifts requires the detection of alternative ultraviolet lines. The strong [C iii]  λ 1907+C iii]  λ 1909 doublet frequently observed in low-metallicity, actively star-forming galaxies is a promising emission feature. We present CLOUDY photoionization model predictions for C iii] equivalent widths (EWs) and line ratios as a function of starburst age, metallicity, and ionization parameter. Our models include a range of C/O abundances, dust content, and gas density. We also examine the effects of varying the nebular geometry and optical depth. Only the stellar models that incorporate binary interaction effects reproduce the highest observed C iii] EWs. The spectral energy distributions from the binary stellar population models also generate observable C iii] over a longer timescale relative to single-star models. We show that diagnostics using C iii] and nebular He ii  λ 1640 can separate star-forming regions from shock-ionized gas. We also find that density-bounded systems should exhibit weaker C iii] EWs at a given ionization parameter, and C iii] EWs could, therefore, select candidate Lyman continuum-leaking systems. In almost all models, C iii] is the next strongest line at <2700 Å after Ly α , and C iii] reaches detectable levels for a wide range of conditions at low metallicity. C iii] may therefore serve as an important diagnostic for characterizing galaxies at z  > 6.

  15. PHOTOIONIZATION MODELS FOR THE SEMI-FORBIDDEN C iii] 1909 EMISSION IN STAR-FORMING GALAXIES

    International Nuclear Information System (INIS)

    Jaskot, A. E.; Ravindranath, S.

    2016-01-01

    The increasing neutrality of the intergalactic medium at z  > 6 suppresses Ly α emission, and spectroscopic confirmation of galaxy redshifts requires the detection of alternative ultraviolet lines. The strong [C iii]  λ 1907+C iii]  λ 1909 doublet frequently observed in low-metallicity, actively star-forming galaxies is a promising emission feature. We present CLOUDY photoionization model predictions for C iii] equivalent widths (EWs) and line ratios as a function of starburst age, metallicity, and ionization parameter. Our models include a range of C/O abundances, dust content, and gas density. We also examine the effects of varying the nebular geometry and optical depth. Only the stellar models that incorporate binary interaction effects reproduce the highest observed C iii] EWs. The spectral energy distributions from the binary stellar population models also generate observable C iii] over a longer timescale relative to single-star models. We show that diagnostics using C iii] and nebular He ii  λ 1640 can separate star-forming regions from shock-ionized gas. We also find that density-bounded systems should exhibit weaker C iii] EWs at a given ionization parameter, and C iii] EWs could, therefore, select candidate Lyman continuum-leaking systems. In almost all models, C iii] is the next strongest line at <2700 Å after Ly α , and C iii] reaches detectable levels for a wide range of conditions at low metallicity. C iii] may therefore serve as an important diagnostic for characterizing galaxies at z  > 6.

  16. Synthesis of [5,6-13C2, 1-14C]olivetolic acid, methyl [1'-13C]olivetolate and [5,6-13C2, 1-14C]cannabigerolic acid

    International Nuclear Information System (INIS)

    Porwoll, J.P.; Leete, E.

    1985-01-01

    Potential advanced intermediates in the biosynthesis of delta 9 -tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous 13 C atoms and 14 C. Methyl [5,6- 13 C 2 , 1- 14 C]olivetolate was prepared from lithium [ 13 C 2 ]acetylide and dimethyl [2- 14 C]malonate. Reaction with geranyl bromide afforded methyl [5,6- 13 C 2 , 1- 14 C]cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The 13 C- 13 C couplings observable in the 13 C NMR spectra of these 13 C-enriched compounds and their synthetic precursors are recorded. Methyl [1'- 14 C]olivetolate was prepared from 13 CO 2 to confirm assignments of the 13 C chemical shifts in the pentyl side chain of these compounds. (author)

  17. Bepaling van 14C in afvalwater

    NARCIS (Netherlands)

    Hiemstra YS; Kwakman PJM; Nissan LN; Aldenkamp FJ; LSO

    1998-01-01

    In opdracht van de Hoofdinspectie Milieuhygiene van het ministerie van VROM heeft LSO een methode ontwikkeld om 14C in afvalwater van nucleaire installaties te bepalen. De methode meet organisch gebonden-14C en anorganisch-14C in de vorm van carbonaat (14CO32-) in afvalwater. Het rapport

  18. Metabolism of [ 14 C]GA 19 and [ 14 C]GA 53 by ecotypes of Betula ...

    African Journals Online (AJOL)

    Continuing with this line of research, we studied the metabolism of 14C-labelled GA19 and GA53. [14C]GA19 and [14C] A53 were applied to the apices of the northern ecotype (67º N) and to the leaves of the southern ecotype (64º N) of Betula pendula Roth. under different photoperiods and at different times in order to ...

  19. Louisiana SIP: LAC 33:III Ch. 14 Subchap B, 1431 to 1434--Conformity to State or Federal Implementation Plans of Transportation Plans, Programs, and Projects Developed, Funded, or Approved Under Title 23 U.S.C. or the Federal Transit Laws

    Science.gov (United States)

    Louisiana SIP: LAC 33:III Ch. 14 Subchap B, 1431 to 1434--Conformity to State or Federal Implementation Plans of Transportation Plans, Programs, and Projects Developed, Funded, or Approved Under Title 23 U.S.C. or the Federal Transit Laws

  20. Stellar C III Emissions as a New Classification Parameter for (WC) Central Stars

    Science.gov (United States)

    Feibelman, W. A.

    1999-01-01

    We report detection of stellar C III lambda 1909 emission in International Ultraviolet Explorer (IUE) echelle spectra of early-type [WC] planetary nebula central stars (CSPNs). Additionally, stellar C III emission at lambda 2297 is observed in early- and late-type [WC) CSPNS. Inclusion of these C III features for abundance determinations may resolve a conflict of underabundance of C/O for early type [WC2] - [WC4] CSPNS. A linear dependence on stellar C III lambda 2297 equivalent widths can be used to indicate a new classification of type [WCUV] central stars.

  1. 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

  2. Sources of C-14 generation and associated doses; Fuentes de generacion de C-14 y dosis asociadas

    Energy Technology Data Exchange (ETDEWEB)

    Amado, Valeria A; Biaggio, Alfredo L; Canoba, Analia C; Curti, Adriana R. [Autoridad Regulatoria Nuclear, Buenos Aires (Argentina)], E-mail: vamado@cae.arn.gov.ar

    2009-07-01

    C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [Spanish] El C-14 es un isotopo radiactivo del C con un periodo de semidesintegracion igual a 5700 anios y que decae a N-14 por emision de radiacion beta. Se produce naturalmente en las altas capas de la atmosfera debido a la reaccion N-14(n,p)C-14 inducida por neutrones lentos de rayos cosmicos. El C-14 antropogenico se genero debido a los ensayos nucleares y actualmente es producido durante la operacion de los reactores nucleares. Una vez liberado se incorpora a la biosfera a traves del ciclo del carbono. A partir de los inicios del periodo industrial la relacion C-14/C-estable, y por ende la dosis debida a C-14 que recibiria la poblacion mundial, ha variado continuamente. El objetivo del presente trabajo es presentar y analizar los distintos factores antropogenicos que modifican la concentracion de C-14, en particular el efecto Suess y la generacion de energia nuclear. Se observa que las

  3. Transfer of 14C to prenatal and neonatal rats from their mothers exposed to 14C compounds by ingestion

    International Nuclear Information System (INIS)

    Takeda, H.; Fuma, S.; Miyamoto, K.; Kuroda, N.; Inaba, J.

    2003-01-01

    The transfer of 14 C through placenta or milk was investigated and the radiation dose to fetal and newborn rats was estimated. Female rats at gestational stages or after delivery were exposed to 14 C in the form of sodium bicarbonate, thymidine and lysine by a single ingestion. Radioactivity in maternal tissues and conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after ingestion. After exposure to these 14 C compounds, there was no significant difference between the 14 C concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of 14 C. The concentration and content of 14 C in the fetus and newborn were, however, dependent on the chemical form of 14 C and on the prenatal or neonatal stage at the time of ingestion. The result of the dose estimation showed that 14 C-lysine gave significantly higher prenatal and neonatal doses than 14 C-sodium bicarbonate or 14 C-thymidine. (author)

  4. Root-uptake of {sup 14}C derived from acetic acid and {sup 14}C transfer to rice edible parts

    Energy Technology Data Exchange (ETDEWEB)

    Ogiyama, Shinichi [Office of Biospheric Assessment for Waste Disposal, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba-shi 263-8555 (Japan)], E-mail: ogiyama@nirs.go.jp; Suzuki, Hiroyuki [Graduate School of Pharmaceutical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba-shi 263-5522 (Japan); Inubushi, Kazuyuki [Graduate School of Horticulture, Chiba University, 648 Matsudo, Matsudo-shi 271-8510 (Japan); Takeda, Hiroshi; Uchida, Shigeo [Office of Biospheric Assessment for Waste Disposal, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba-shi 263-8555 (Japan)

    2010-02-15

    Three types of culture experiments using paddy rice (Oryza sativa L.) were performed to examine root-uptake of {sup 14}C in the form of acetic acid: double pot experiment (hydroponics), wet culture experiment (submerged sand medium), and chamber experiment (hydroponics and submerged sand medium). The {sup 14}C radioactivity in the plant, mediums, and atmospheric carbon dioxide ({sup 14}CO{sub 2}) in the chamber were determined, and the distribution of {sup 14}C in the plant was visualized using autoradiography. In the double pot experiment, the shoot of the plant and the lower root which was soaked in the culture solution had {sup 14}C radioactivity, but the upper root which did not have contact with the solution had none. There were also {sup 14}C radioactivity in the grains and roots in the wet culture experiment. Results of the chamber experiment showed that {sup 14}CO{sub 2} gas was released from the culture solution in both types of cultures. Results indicated that the {sup 14}C-acetic acid absorbed by rice plant through its root would be very small. Most of the {sup 14}C-acetic acid was transformed into gaseous forms either in the culture solution or rhizosphere. A relatively longer time would be needed to assimilate {sup 14}C derived from acetic acid to grain parts after it was once absorbed by the shoot through the root. Availability of {sup 14}C for the plant in sand culture was considered to be decreased compared with that for the plant in the hydroponics experiment. It was suggested that rice plant absorbed and assimilated {sup 14}C through the plant roots not because of uptake of {sup 14}C-acetic acid but because of uptake of {sup 14}C in gaseous forms such as {sup 14}CO{sub 2}.

  5. Method of preparing D-mannose(U-14C) from glucons(U-14C) separated from natural material

    International Nuclear Information System (INIS)

    Kucar, S.; Zemek, J.; Bilik, V.; Kolina, J.

    1981-01-01

    Glucans(U- 14 C) separated from green or blue-green algae are hydrolysed using diluted mineral acids in the presence of small amounts of molybdate ions to D-glucose(U- 14 C) which, at a temperature of 60 to 100 degC epimerizes to D-mannose(U- 14 C). The epimeric aldoses are separated from the reaction mixture by paper chromatography. (H.S.)

  6. 14C Records from Indonesian Sea

    International Nuclear Information System (INIS)

    Baresic, J.; Fallon, S.; Mazerat, J.

    2013-01-01

    To investigate ocean currents and past climate events affecting the Indonesian throughflow (ITF), a radiocarbon record from a Porites coral collected from Alor Island, Indonesia, was constructed. Porites corals are often used in paleoclimate research and water mass circulation studies in the Tropics because of their abundance in the region and growth rate of 8 - 20 mm/y. These characteristics allow reconstructions of past environmental changes on weekly to annual time scales. At this point radiocarbon coral results from Alor cover approximately 30 years. An age model was constructed using the sea surface temperature proxy δ18O. Alor radiocarbon results were compared with previous measurements obtained from Padang and Langkai corals. a14C values obtained from the Alor coral display a strong seasonal cycle, high values during Australian summer and low values during Australian winter. Higher a 14C summer values indicate inflow of waters enriched by 14C through Makassar Strait from the North Pacific Ocean and Java Sea surface water. Summer a14C values are also enhanced by summer stratification. Winter values indicate upwelling of deep Ocean waters within the research area and transport of 14C-depleted waters from the Banda Sea, which has input from the South Pacific Ocean (lower a14C than North Pacific). Therefore, the a14C coral record reflects the movement of enriched water from North Pacific to Indian Ocean through Makassar Strait during summer and upwelling of depleted surface waters from the Banda Sea during the winter. Lower a14C dips could be attributed to strong El Nino events, which would enhance surface water mixing and upwelling of low radiocarbon deep waters. Water transport from North Pacific Ocean decreases during El Nino events also contributing to lowering of a14C signal.(author)

  7. 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)

  8. Synthesis of [14C]-62514, a radiolabelled derivative of erythromycin A, via [2-14C]N,N-dimethylethylenediamine

    International Nuclear Information System (INIS)

    Surber, B.W.; Baker, W.R.; Seif, L.

    1991-01-01

    The synthesis of [ 14 C]A-62514, 11-deoxy-11[carboxy(2-dimethylamino-[1- 14 C]ethyl)amino]-6-0-methyl-e rythromycin A 11,12-(cyclic ester), was performed in five steps. The key intermediate, [2- 14 C]N,N-dimethylethyl-enediamine, was obtained in 80% yield by reacting Eschenmoser's salt with K 14 CN and reducing the resulting [1- 14 C]N,N-dimethylglycinonitrile with H 2 and Raney Ni in methanol and ammonium hydroxide. The final product was obtained 97% radiochemically pure in an overall radiochemical yield of 14%, with a specific activity of 39 mCi/mmol. (author)

  9. Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L; Audinot, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

  10. Synthesis of DL-adrenaline (methyl C{sup 14}) (1961); Synthese de la DL-adrenaline (methyle {sup 14}C) (1961)

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L.; Audinot, M. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    The sodium derivative of 5-3-4 dibenzyl oxyphenyl 2-oxazolidinone reacted with methyl iodide {sup 14}C, in stoichiometric quantity, gives rise to the corresponding N-methyl {sup 14}C derivative. The oxazolidinone ring is opened by concentrated hydrochloric acid and the benzyl groups removed by catalytic hydrogenolysis. Adrenaline methyl {sup 14}C is then purified on Dowex 50 X-12 exchange resin. Overall-yield is 45 per cent based upon methyl iodide {sup 14}C. (author) [French] Le derive sode de la (dibenzyloxy-3-4-phenyl)-5 oxazolidinone-2 traite par l'iodure de methyle {sup 14}C, en proportion stoechiometrique, fournit le derive N-methyle {sup 14}C correspondant. Apres ouverture du cycle oxazolidinone par HCL concentre et debenzylation par hydrogenation catalytique, on purifie l'adrenaline (methyle {sup 14}C) par chromatographie sur resine echangeuse Dowex 50 X-12. Le rendement est de 45 pour cent par rapport a l'iodure de methyle {sup 14}C. (auteurs)

  11. Synthesis of ethanol {sup 14}C-1; Synthese d'ethanol {sup 14}C-1

    Energy Technology Data Exchange (ETDEWEB)

    Wolff, R E; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    The direct reduction by LiAlH{sub 4}, of a suspension of anhydrous sodium acetate in tetra-hydro-furfuryl-oxy-tetra-hydro-pyran is described. This study has shown that the ethanol thus obtained is impure and that the yields are erratic. On the contrary the reduction of acetyl chloride 1-{sup 14}C by LiAlH{sub 4}, in 'diethyl carbitol' leads to ethanol 1-{sup 14}C of satisfactory purity with a yield of about 71 percent. (author) [French] Une etude de la reduction directe par LiAlH{sub 4}, de l'acetate de soude anhydre en suspension dans le tetrahydrofurfuryloxytetrahydropyrane est decrite. Cette etude a montre que l'on obtient de l'ethanol souille d'impuretes, avec un rendement variable. Par contre, la reduction du chlorure d'acetyle {sup 14}C-1 par LiAlH{sub 4}, dans le 'diethyl carbitol' conduit a l'ethanol {sup 14}C-1 de purete convenable avec un rendement de l'ordre de 71 pour cent. (auteur)

  12. Antisense oligonucleotide inhibition of apolipoprotein C-III reduces plasma triglycerides in rodents, nonhuman primates, and humans.

    Science.gov (United States)

    Graham, Mark J; Lee, Richard G; Bell, Thomas A; Fu, Wuxia; Mullick, Adam E; Alexander, Veronica J; Singleton, Walter; Viney, Nick; Geary, Richard; Su, John; Baker, Brenda F; Burkey, Jennifer; Crooke, Stanley T; Crooke, Rosanne M

    2013-05-24

    Elevated plasma triglyceride levels have been recognized as a risk factor for the development of coronary heart disease. Apolipoprotein C-III (apoC-III) represents both an independent risk factor and a key regulatory factor of plasma triglyceride concentrations. Furthermore, elevated apoC-III levels have been associated with metabolic syndrome and type 2 diabetes mellitus. To date, no selective apoC-III therapeutic agent has been evaluated in the clinic. To test the hypothesis that selective inhibition of apoC-III with antisense drugs in preclinical models and in healthy volunteers would reduce plasma apoC-III and triglyceride levels. Rodent- and human-specific second-generation antisense oligonucleotides were identified and evaluated in preclinical models, including rats, mice, human apoC-III transgenic mice, and nonhuman primates. We demonstrated the selective reduction of both apoC-III and triglyceride in all preclinical pharmacological evaluations. We also showed that inhibition of apoC-III was well tolerated and not associated with increased liver triglyceride deposition or hepatotoxicity. A double-blind, placebo-controlled, phase I clinical study was performed in healthy subjects. Administration of the human apoC-III antisense drug resulted in dose-dependent reductions in plasma apoC-III, concomitant lowering of triglyceride levels, and produced no clinically meaningful signals in the safety evaluations. Antisense inhibition of apoC-III in preclinical models and in a phase I clinical trial with healthy subjects produced potent, selective reductions in plasma apoC-III and triglyceride, 2 known risk factors for cardiovascular disease. This compelling pharmacological profile supports further clinical investigations in hypertriglyceridemic subjects.

  13. Metabolic kinetics and biological effects of radiocarbon (14C)

    International Nuclear Information System (INIS)

    Vasilenko, I.Ya.; Osipov, V.A.; Lyaginskaya, A.M.; Bugryshev, P.F.; Istomina, A.G.; Turova, V.I.; Dement'ev, S.I.; Zhorova, E.S.; Mart'yanov, B.M.; Shal'nova, G.A.; Kuz'mina, T.D.; Shebenko, V.A.; Pomerantseva, M.D.; Ramajya, L.K.

    1988-01-01

    Radiocarbon 14 C is one of the most widespread radionuclides. Increased concentration of anthropogenic 14 C in the biosphere is a problem of considerable hygienic and ecological significance. The paper presents the results of comprehensive studies for years on biokinetics of the main 14 C compounds, inorganic (Na H 14 CO 3 , Na 2 14 CO 3 , K 2 14 CO 3 , Ca 14 CO 3 ) as well as organic ( 14 C-glucose, 14 C-succinic acid, 14 C-glucosamine, 14 C-glycine, 14 C-tryptophane, 14 C-valine, 14 C-palmitic acid, 14 C-stearic acid, 14 C-ethyl alcohol, 14 C-methyl alcohol, 14 C-urea), of 14 C as food constituent and of elementary radiocarbon. The 14 C toxicity is investigated for both acute and chronic small doses received by animals. The nuclide's genetic efficiency is assessed. Based on research evidence, the accumulation multiple and equilibrium time are estimated for long-term 14 C intake by humans. The data may be used for setting genetic standards and estimating an anthropogenic increase of 14 C concentration in the environment. The hazard of anthropogenic radiocarbon is assessed with allowance for further development of nuclear power industry. (author)

  14. S-adenosyl-L-(l-14C)-homocysteine

    International Nuclear Information System (INIS)

    Thomas, H.J.; Montgomery, J.A.

    1987-01-01

    S-Adenosyl-L-(1- 14 C)-homocysteine was prepared from commercially available L-(1- 14 C)-methionine by conversion first to S-benzyl-L-(1- 14 C)-homocysteine which upon treatment with sodium in liquid ammonia gave the disodium salt of L-(1- 14 C)-homocysteine. Reaction of this sodium salt with 5'-O-tosyladenosine gave the title compound. (author)

  15. Synthesis of /sup 14/C-labeled felbamate from phenylacetic-(methylene-/sup 14/C) acid

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Y.M.; Kucharczyk, N.; Sofia, R.D.

    1986-05-01

    A synthetic procedure for the preparation of 2-phenyl-1,3-propanediol-2-/sup 14/C dicarbamate, starting with phenylacetic-(methylene-/sup 14/C) acid was developed. The procedure from phenylacetic acid to 2-phenyl-1,3-propanediol dicarbamate has four steps via phenylmalonic acid and 2-phenyl-1,3-propanediol. The overall yield of all four steps was 28%.

  16. Direct preparation of 14C-labelled 5-allyl- and 5-propyl-2'-deoxyuridine from [2-14C]2'-deoxyuridine

    International Nuclear Information System (INIS)

    Ruth, J.L.; White, S.K.; Bergstrom, D.E.

    1982-01-01

    [2- 14 C]5-Allyl-2'-deoxyuridine was synthesized directly from [2- 14 C]2'-deoxyuridine using mercury, palladium, and 3-chloropropene. [2- 14 C]5-Propyl-2'-deoxyuridine was obtained by hydrogenation of the [ 14 C]5-allyl-2'-deoxyuridine. Advantages of the synthetic method and its application to the preparation of other radiolabeled 5-alkyl/alkenyl-2'-deoxyuridines are discussed. (author)

  17. Synthesis of [14C]Zolpidem

    International Nuclear Information System (INIS)

    Allen, J.; Tizot, A.

    1986-01-01

    The synthesis of [ 14 C]Zolpidem, a new hypnotic agent having a non-benzodiazepine structure, is described. This compound was synthesised in a 64% overall radiochemical yield from potassium [ 14 C]cyanide and with a specific radioactivity of 56 mCi/mmol. It was used for pharmacokinetic and drug metabolism studies. (author)

  18. Determination of the solubility of Np(IV), Pu(III) - (VI),Am(III) - (VI), and Te(IV), (V) hydroxo compounds in 0.5 - 14 M NaOH solutions

    Energy Technology Data Exchange (ETDEWEB)

    Delegard, C.H.

    1996-09-24

    The solubilities of Am(III), Np(IV), Pu(IV), Tc(IV), Np(V), Pu(V), Am(V), and Tc(V) hydroxo compounds were studied in 0.5 to 14 M NaOH solutions at 25{+-}2 {degrees}C. The effects of fluoride, phosphate, carbonate, oxalate, and some other organic complexing agents on the solubilities of Np(IV), Pu(IV), and TC(IV) hydroxides were investigated at 1.0 and 4.0 M NAOH. Some predictions were made on the dissolved (I.V) and (V) species present in alkali solutions.

  19. 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)

  20. Anti-thrombin III, Protein C, and Protein S deficiency in acute coronary syndrome

    Directory of Open Access Journals (Sweden)

    Dasnan Ismail

    2002-06-01

    Full Text Available The final most common pathway for the majority of coronary artery disease is occlusion of a coronary vessel. Under normal conditions, antithrombin III (AT III, protein C, and protein S as an active protein C cofactor, are natural anticoagulants (hemostatic control that balances procoagulant activity (thrombin antithrombin complex balance to prevent thrombosis. If the condition becomes unbalanced, natural anticoagulants and the procoagulants can lead to thrombosis. Thirty subjects with acute coronary syndrome (ACS were studied for the incidence of antithrombin III (AT III, protein C, and protein S deficiencies, and the result were compare to the control group. Among patients with ACS, the frequency of distribution of AT-III with activity < 75% were 23,3% (7 of 30, and only 6,7% ( 2 of 30 in control subject. No one of the 30 control subject have protein C activity deficient, in ACS with activity < 70% were 13,3% (4 of 30. Fifteen out of the 30 (50% control subjects had protein S activity deficiency, while protein S deficiency activity < 70% was found 73.3.% (22 out of 30. On linear regression, the deterministic coefficient of AT-III activity deficiency to the development ACS was 13,25 %, and the deterministic coefficient of protein C activity deficient to the development of ACS was 9,06 %. The cut-off point for AT-III without protein S deficiency expected to contribute to the development of vessel disease was 45%. On discriminant analysis, protein C activity deficiency posed a risk for ACS of 4,5 greater than non deficient subjects, and AT-III activity deficiency posed a risk for ACS of 3,5 times greater than non deficient subjects. On binary logistic regression, protein S activity acted only as a reinforcing factor of AT-III activity deficiency in the development of ACS. Protein C and AT III deficiency can trigger ACS, with determinant coefficients of 9,06% and 13,25% respectively. Low levels of protein C posed a greater risk of

  1. A rapid microwave induced synthesis of [carboxyl-14C]-nicotinic acid (vitamin B3) and [carbonyl-14C]-nicotinamide using K14CN

    International Nuclear Information System (INIS)

    Ravi, S.; Mathew, K.M.; Sivaprasad, N.

    2008-01-01

    Microwave assisted direct aromatic substitution of 3-bromopyridine with K 14 CN as the cyanide source and catalytic amount of tetrabutylammonium bromide afforded [3- 14 C]-cyanopyridine 3 in 90% yield. Microwave assisted hydrolysis of 3 with a mixture of concentrated hydrochloric acid and propionic acid afforded [carboxyl- 14 C]-nicotinic acid in 95% yield whereas microwave assisted hydrolysis of 3 with a mixture of concentrated sulfuric acid and propionic acid afforded [carbonyl- 14 C]-nicotinamide in 85% yield. (author)

  2. Appraisal of the 14C-glycocholate acid test with special reference to the measurement of faecal 14C excretion

    International Nuclear Information System (INIS)

    Scarpello, J.H.B.; Sladen, G.E.

    1977-01-01

    The 14 C-glycocholate test, including the measurement of marker corrected faecal 14 C, has been assessed in the following groups of subjects: normal controls (18), patients with diarrhoea not attributable to altered bile acid metabolism (21), patients with diverticula of the small intestine (12), patients with previous resection of ileum and often proximal colon (34), and established ileostomists (10). Patients with diverticular disease had increased breath 14 CO 2 excretion, but normal faecal excretion of 14 C, and this test was more frequently abnormal than the Schilling test. Ileostomists excreted increased amounts of faecal 14 C, even when the ileum was intact and apparently normal. The pattern after resection was complex. Breath 14 C output was normal if the ileal resection was less than 25 cm in length, although some of these patients had increased faecal 14 C excretion if, in addition, at least 15 cm of proximal colon had been resected or by-passed. Longer ileal resections were associated with increased breath and/or faecal 14 C excretion, depending in part on the length of colon resected or by-passed and the 24 hour faecal volume. Fewer than half these patients had both increased breath and faecal excretion of isotope and faecal 14 C alone was occasionally normal with an ileal resection of 50 cm or more. The 14 C-glycocholate test was more frequently abnormal than the Schilling test in this group. The use of faecal marker correction had only a minor impact on the results. These data suggest that, in patients with ileal resection, faecal 14 C, like faecal weight, is determined by the extent of colonic resection as well as by the amount of ileum resected. (author)

  3. Synthesis of 14C-labelled milrinone

    International Nuclear Information System (INIS)

    Duncan, D.R.; Johnston, D.; Andrews, R.S.

    1985-01-01

    A synthetic procedure for producing 14 C-labelled milrinone, a potent new cardiotonic agent, is described. The synthesis was achieved in two steps from 1-(4-pyridyl)propan-2-one utilising [2- 14 C]cyanoacetamide as the source of the radiolabel. The overall chemical yield was 46% and the radiochemical yield 35%. (author)

  4. Behaviour of 14C-sulfadiazine and 14C-difloxacin during manure storage

    International Nuclear Information System (INIS)

    Lamshoeft, Marc; Sukul, Premasis; Zuehlke, Sebastian; Spiteller, Michael

    2010-01-01

    The persistence of sulfadiazine, difloxacin, and their metabolites has been investigated in stored manure. The manure collected from sulfadiazine ( 14 C-SDZ) and difloxacin ( 14 C-DIF) treated pigs contained N-acetylsulfadiazine (Ac-SDZ), 4-hydroxy-SDZ (4-OH-SDZ), and sarafloxacin (SARA) as the main metabolites, respectively along with their parent compounds. Manures were stored separately at 10 o C and 20 o C at various moisture levels. About 96-99% of the radioactivity remained in extractable parent compounds and their metabolites after 150 d of storage. The formation of non-extractable residue and the rate of mineralization were both negligible in manure containing SDZ and DIF. During storage SDZ concentration increased as a result of the deacetylation of Ac-SDZ, whose concentration decreased proportionally. Hence the environmental effects may be underestimated if the parent compound alone is considered for environmental risk assessment. About 11% and 14% of 4-OH-SDZ were lost after 20 and 40 d of storage; thereafter its concentration increased relatively, highlighting hydroxylation of SDZ. DIF degraded very slowly (7% loss after 150 d) during the storage of manure; in contrast the concentration of SARA decreased rapidly (72-90% loss after 150 d). Dilution of manure and storage at higher temperatures for a reasonable period of time enhanced the rate of reactions of SDZ, DIF and their related metabolites.

  5. Synthesis of [methyl-{sup 14}C]crotonobetaine from DL-[methyl-{sup 14}C]carnitine

    Energy Technology Data Exchange (ETDEWEB)

    Loester, H.; Seim, H. [Leipzig Univ. (Germany). Inst. of Clinical Chemistry and Pathobiochemistry

    1996-02-01

    The causes of carnitine deficiency syndromes are not completely understood, but decomposition of L-carnitine in vivo is likely to be involved. Carnitine is metabolized to {gamma}-butyrobetaine, and crotonobetaine is probably an intermediate in this pathway. To validate experimentally the precursor-product relationship between the three physiologically occuring {gamma}-betaines - L-carnitine, crotonobetaine, {gamma}-butyrobetaine - labelling with stable or radioactive isotopes became necessary. Methyl-labelled carnitine isomers (L(-)-, D(+)- or DL-) or {gamma}-butyrobetaine can be easily synthesized by methylation of 4-amino-3-hydroxybutyric acid isomers or 4-aminobutyric acid, respectively. Because of problems with the 4-aminocrotonic acid, we synthesized labelled crotonbetaine from labelled carnitine. Thus, DL-[methyl-{sup 14}C]carnitine was dehydrated by reaction with concentrated sulfuric acid. After removal of the latter the products were separated and purified by ion exchange chromatography on DOWEX 50 WX8 (200 - 400 mesh) and gradient elution with hydrochloric acid. In addition to the labelled main product [methyl-{sup 14}C]crotonobetaine (yield about 50 %), [methyl-{sup 14}C]glycine betaine and [methyl-{sup 14}C]acetonyl-trimethylammonium (ATMA) were formed. The end products were identified by combined thin layer chromatography/autoradiography and quantified by liquid scintillation counting. (Author).

  6. 14C concentrations in tree stems, 1

    International Nuclear Information System (INIS)

    Kikata, Yoji; Yonenobu, Hitoshi; Morishita, Fumio; Hattori, Yoshiaki; Marsoen, S.N.

    1993-01-01

    The 14 C concentrations in trees sampled at various latitudes were measured with a Tandetron Accelerator Mass Spectrometer at Nagoya University. The growing periods of the parts for 14 C measurements were estimated by the relationship between meteorological conditions and the appearance of anatomical features of annual rings such as false rings, latewood formation, and so on. The following results were obtained: 1. The latitude dependence of the 14 C variation is found in tree stems as well as in the atmosphere. 2. The 14 C concentrations in tree stems are almost equal to those in the atmosphere at the latitude where the tree had grown and at the time when the sampled section is formed. Therefore the 14 C concentrations in the atmosphere are estimated by those of the tree stems. 3. The time when the 14 C concentration in the tree showed its maximum value has difference of 1 - 2 years with that of the latitude where the tree had grown. 4. This phenomena seemed to be related closely with the mechanism of global mixing of 14 CO 2 produced by atmospheric nuclear weapon tests. This mechanism causes a time lag of 14 C variation between northern and southern hemisphere. (author)

  7. Estimation of radiation dosage and transmutation effect of 14C involved in measuring rate of albumin synthesis with 14C-carbonate

    International Nuclear Information System (INIS)

    Yap, A.H.; Hafkenscheid, J.C.M.; Goossens, C.M.I.C.; Buys, W.C.A.M.; Binkhorst, R.A.; Van Tongeren, J.H.M.

    1975-01-01

    For direct measurement of the rate of albumin synthesis, Na 2 14 CO 3 was used intravenously. The assessment of the radiation hazard involved in the study was based on the knowledge of the minimum dose of Na 2 14 CO 3 necessary for a sufficient incorporation of 14 C in the guanidine-C of arginine in albumin to obtain measurable radioactivity. By measurement of expired 14 CO 2 and excreted 14 C-urea in the urine during a 5-hr period following intravenous administration of Na 2 14 CO 3 in five subjects, some quantitative data on 14 C retention and radiation dosage were obtained. In comparison with animal studies, the rate of expiration of 14 CO 2 in man is slower. About 50 percent of the total radioactivity injected was lost through the respiratory route in the first hour. The total amount of expired 14 C during the 5 hr of investigation was about 75 percent of the injected dose for the five subjects. The amount of 14 C excreted as urinary 14 C-urea during the 5 hr of investigation is very small in comparison with the expired 14 C; it was only about 0.5 percent of the dose injected. The total absorbed radiation dose after complete elimination of 14 C from the body was calculated with various assumptions. The extra risk of genetic damage due to disintegration of retained 14 C in comparison with that of natural 14 C in the body during 30 living years is about 50 percent. (U.S.)

  8. Human pro. cap alpha. 1(III) collagen: cDNA sequence for the 3' end

    Energy Technology Data Exchange (ETDEWEB)

    Mankoo, B S; Dalgleish, R

    1988-03-25

    The authors have previously isolated two overlapping cDNA clones, pIII-21 and pIII-33, which encode the C-terminal end of human type III procollagen. They now present the sequence of 2520 bases encoded in these cDNAs which overlaps other previously published sequences for the same gene. The sequence presented differs from previously published sequences at five positions.

  9. Rhodium(III)-Catalyzed Amidation of Unactivated C(sp(3) )-H Bonds.

    Science.gov (United States)

    Wang, He; Tang, Guodong; Li, Xingwei

    2015-10-26

    Nitrogenation by direct functionalization of C-H bonds represents an important strategy for constructing C-N bonds. Rhodium(III)-catalyzed direct amidation of unactivated C(sp(3) )-H bonds is rare, especially under mild reaction conditions. Herein, a broad scope of C(sp(3) )-H bonds are amidated under rhodium catalysis in high efficiency using 3-substituted 1,4,2-dioxazol-5-ones as the amide source. The protocol broadens the scope of rhodium(III)-catalyzed C(sp(3) )-H activation chemistry, and is applicable to the late-stage functionalization of natural products. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Apolipoprotein C-III Levels and Incident Coronary Artery Disease Risk: The EPIC-Norfolk Prospective Population Study.

    Science.gov (United States)

    van Capelleveen, Julian C; Bernelot Moens, Sophie J; Yang, Xiaohong; Kastelein, John J P; Wareham, Nicholas J; Zwinderman, Aeilko H; Stroes, Erik S G; Witztum, Joseph L; Hovingh, G Kees; Khaw, Kay-Tee; Boekholdt, S Matthijs; Tsimikas, Sotirios

    2017-06-01

    Apolipoprotein C-III (apoC-III) is a key regulator of triglyceride metabolism. Elevated triglyceride-rich lipoproteins and apoC-III levels are causally linked to coronary artery disease (CAD) risk. The mechanism(s) through which apoC-III increases CAD risk remains largely unknown. The aim was to confirm the association between apoC-III plasma levels and CAD risk and to explore which lipoprotein subfractions contribute to this relationship between apoC-III and CAD risk. Plasma apoC-III levels were measured in baseline samples from a nested case-control study in the European Prospective Investigation of Cancer (EPIC)-Norfolk study. The study comprised 2711 apparently healthy study participants, of whom 832 subsequently developed CAD. We studied the association of baseline apoC-III levels with incident CAD risk, lipoprotein subfractions measured by nuclear magnetic resonance spectroscopy and inflammatory biomarkers. ApoC-III levels were significantly associated with CAD risk (odds ratio, 1.91; 95% confidence interval, 1.48-2.48 for highest compared with lowest quintile), retaining significance after adjustment for traditional CAD risk factors (odds ratio, 1.47; 95% confidence interval, 1.11-1.94). ApoC-III levels were positively correlated with triglyceride levels, ( r =0.39), particle numbers of very-low-density lipoprotein ( r =0.25), intermediate-density lipoprotein ( r =0.23), small dense low-density lipoprotein ( r =0.26), and high-sensitivity C-reactive protein ( r =0.15), whereas an inverse correlation was observed with large low-density lipoprotein particle number ( r =-0.11), P C-reactive protein. ApoC-III levels are significantly associated with incident CAD risk. Elevated levels of remnant lipoproteins, small dense low-density lipoprotein, and low-grade inflammation may explain this association. © 2017 American Heart Association, Inc.

  11. Transfer of {sup 14}C to prenatal and neonatal rats from their mothers exposed to {sup 14}C compounds by ingestion

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, H.; Fuma, S.; Miyamoto, K.; Kuroda, N.; Inaba, J

    2003-07-01

    The transfer of {sup 14}C through placenta or milk was investigated and the radiation dose to fetal and newborn rats was estimated. Female rats at gestational stages or after delivery were exposed to {sup 14}C in the form of sodium bicarbonate, thymidine and lysine by a single ingestion. Radioactivity in maternal tissues and conceptuses (placenta, fetal membrane and fetus) and in the newborn was determined at various times after ingestion. After exposure to these {sup 14}C compounds, there was no significant difference between the {sup 14}C concentration in the fetus and that in the maternal tissues, suggesting that the placenta has no effect in preventing or accelerating the placental transfer of {sup 14}C. The concentration and content of {sup 14}C in the fetus and newborn were, however, dependent on the chemical form of {sup 14}C and on the prenatal or neonatal stage at the time of ingestion. The result of the dose estimation showed that {sup 14}C-lysine gave significantly higher prenatal and neonatal doses than {sup 14}C-sodium bicarbonate or {sup 14}C-thymidine. (author)

  12. Synthesis of [methyl-[sup 14]C]-N-methylputrescine

    Energy Technology Data Exchange (ETDEWEB)

    Secor, H.V.; Izac, R.R.; Hassam, S.B.; Frisch, A.F. (Philip Morris Research Center, Richmond, VA (United States))

    1994-05-01

    [Methyl-[sup 14]C]-N-methylputrescine was prepared from [[sup 14]C]methylamine hydrochloride in five steps. Reaction of benzaldehyde and [[sup 14]C]methylamine (10 mCi) followed by catalytic hydrogenation yielded [methyl-[sup 14]C]-N-methylbenzylamine. The key step in this process is the alkylation of [methyl-[sup 14]C]-N-methylbenzylamine in aqueous medium with 4-bromobutyronitrile. The radiochemical purity of the final product after two successive catalytic hydrogenations was in excess of 97%. The radiochemical yields in two successive runs were 26 and 38%, based on starting [[sup 14]C]methylamine, with specific activities of 22 and 23 mCi/mmol, respectively. This sequence provides a convenient and efficient regioselective radiosynthesis of [methyl-[sup 14]C]-N-methylputrescine. (author).

  13. Effects of Pseudomonas species on the release of bound 14C residues from soil treated with [14C]atrazine

    International Nuclear Information System (INIS)

    Khan, S.U.; Behki, R.M.

    1990-01-01

    The release of bound (nonextractable) 14 C residues from soil previously treated with [ 14 C]atrazine was investigated by incubation of the solvent-extracted soil with two species of Pseudomonas capable of metabolizing atrazine. The two species, 192 and 194, released bound 14 C residues from the soil. Addition of glucose, known to increase microbiological activities, to the incubated soil appeared to enhance the release of soil-bound 14 C residues, in particular in the presence of Pseudomonas species 192. The 14 C bound residues in soil, mainly present as the parent compound and its hydroxy and monodealkylated analogues, were released into the incubation mixture and were subsequently metabolized by the two species involving dechlorination and dealkylation

  14. Spectrophotometric study of the complexation equilibria of lanthanum(III) with 1,4-bis(4'-methylanilino)anthraquinone and the determination of lanthanum(III)

    International Nuclear Information System (INIS)

    Idriss, K.A.-R; El-Shahawy, A.S.; Sedaira, H.; Harfoush, A.A.

    1985-01-01

    The complexation equilibria of lanthanum(III) with 1,4-bis(4'-methylanilino)anthraquinone (Quinizarin Green) were studied spectrophotometrically in 40% V/V dimethylformamide using graphical analysis of the absorbance curves. The reaction mechanism of lanthanum with the bisarylaminoanthraquinone dye within the pH range 6 to 9.25 was demonstrated. The thermodynamic stabilities and the molar absorptivities of the complexes formed were determined. The optimum conditions for the spectrophotometric determination of La(III) with this reagent were found. (author)

  15. Early incorporation and distribution of 14C-photosynthates after 14C-feeding for a brief period in tea plant

    International Nuclear Information System (INIS)

    Hakamata, Katsuhiro

    1981-01-01

    In order to clarify the early incorporation and distribution of 14 C-photosynthetic products in tea plants after 14 C-feeding for a brief period, 14 C-tracer experiments were performed, using the winter leaves, first crop shoots and young tea plants of a cultivar, Yabukita. As the results of the experiment on leaf disks by 14 C-Feeding for one minute, the 14 C-activity in the ethanol soluble fraction distributed in the anionic, cationic and neutral fractions in this order. When the time of feeding was extended to 10 min, the distribution in the cationic fraction decreased, and that in the neutral fraction increased. In the experiment on shoots, after the end of 10 min assimulation, the 14 C-activity in the ethanol soluble fraction distributed in the neutral, cationic and anionic fractions in this order. In course of time, the distribution in the cationic and anionic fractions decreased, and that in the neutral fraction increased. As the results of 14 C-feeding to young tea plants for 2.5 hours, 70 - 95% of the 14 C-activity in the ethanol soluble fraction distributed in the neutral fraction. Sucrose seemed to be the primary and early product of photosynthesis, and might be the principal carbohydrate form of translocation and reserve in tea plants. Raffinose and stachyose played almost the same role as sucrose. (Kako, I.)

  16. Genetic consequences of the 14C-decay

    International Nuclear Information System (INIS)

    Gracheva, L.M.; Korolev, V.G.

    1978-03-01

    There are only few investigations on the biological and genetic consequences of 14 C decay especially due to the long half-life of 14 C. Naturally, the consequences of the decay of 14 C incorperated in DNA is of particular interest. Due to the thus occuring conversion into nitrogen, either opening of the ribose residue ring and base occurs or conversion into base analogue. The present work gives a survey on the investigational results on this topic which were obtained by various authors on phages, bacteria, algae and animal cells, as well as on molecular level. It was shown that the transmutation for the occurence of a lethal effect is many times more effective than β-radiation. Investigations of the mutagenic effects and other genetic effects of the 14 C decay were carried out on micro-organisms, however also on higher forms of life, plants, insects and mice. An analysis of the mutations showed that transitions as well as transversions occur. As example for genetic effects of 14 C decay, the two following are named. In the case of mice which were exposed to 14 CO 2 atmosphere, it was seen that the number of polyptoidal chromosome sets in the first spermotacytes increased considerably, an increase of the chromosome conversion rate was however not observed. When treating gryllus larvae with 14 C, it was interesting to note that the crossing of 14 C-contained females with normal males produced viable eggs, whereas normal females after crossing with 14 C contained males, laid no more eggs. (MG) 891 MG [de

  17. Reviewing the Mid-First Millennium BC {sup 14}C 'warp' using {sup 14}C/bristlecone pine data

    Energy Technology Data Exchange (ETDEWEB)

    Taylor, R.E., E-mail: retaylor@ucr.edu [Department of Anthropology, University of California, Riverside, Riverside, CA (United States); Cotsen Institute of Archaeology, University of California, Los Angeles, CA (United States); Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory, University of California, Irvine, CA (United States); Southon, John [Keck Carbon Cycle Accelerator Mass Spectrometry Laboratory, University of California, Irvine, CA (United States)

    2013-01-15

    AMS-based {sup 14}C measurements have been obtained on 53 dendrochronologically-dated Bristlecone pine (Pinus longaeva) wood samples in decadal increments spanning 2300-2750 cal BP with particular interest focused on the decades centered on 2405 cal BP and 2625 cal BP. In general, there is overall agreement with the current IntCal04/09 consensus calibration curve for this period. For the 2400-2410 cal BP interval, our Bristlecone-based {sup 14}C value is consistent with the {sup 14}C value obtained by Belfast on Irish oak for that decade but not on German oak values obtained by Seattle. Our {sup 14}C value for the 2620-2630 cal BP interval is consistent with the German oak (Heidelberg)-based {sup 14}C decadal value. The {sup 10}Be-based reconstruction of {sup 14}C variations over the 2620-2630 cal BP interval also supports the Heidelberg data although clearly additional clarifications are required before the current tree ring-based {sup 14}C and ice core-based {sup 10}Be data for this interval can be accurately interpreted and valid inferences obtained.

  18. 14C levels in Trombay environment

    International Nuclear Information System (INIS)

    Doshi, G.R.; Sadarangani, S.H.; Krishnamoorthy, T.M.

    1994-01-01

    The passive air sampling method has been used to measure the spatial distribution of the specific activity of 14 C in air samples collected within the Trombay complex. The samples collected within radial distance of about 0.5 km from Cirus showed 3 to 5 times higher specific activity of 14 C over the natural background level of 6.2 pCi/g C. The same decreased with the distance and approached the value of natural level at the site boundary (1.6 km). The specific activity of 14 C in leaf samples collected within the complex showed the similar pattern. (author). 6 refs., 2 tabs

  19. [14C]Virginiamycin residues in eggs

    International Nuclear Information System (INIS)

    Corpet, D.E.; Baradat, M.; Bories, G.F.

    1988-01-01

    Laying hens were fed ab libitum a diet supplemented at 40, 10, and 0 mg/kg with [ 14 C]virginiamycin, to determine whether or not virginamycin or its metabolites were transferred to the eggs. About 0.05% of the ingested 14 C dose was recovered in the eggs. Radiolabeled residues expressed in terms of virginiamycin equivalents were found to be 5.1 ng/g in the albumen and 31.8 ng/g in the yolk from hens fed a 10 mg/kg diet. No antibiotic activity could be detected in the eggs. Tentative identifications showed that in the albumen about 17% of the 14 C behaved chromatographically like virginiamycin and 18% was associated to the ovalbumin. In the yolk 31% of the 14 C was associated to proteins, 58% to fatty acids, and 4% to unsaponifiable matter

  20. 14C emission from Swedish nuclear power plants and its effect on the 14C levels in the environment

    International Nuclear Information System (INIS)

    Stenstroem, K.; Erlandsson, Bengt; Hellborg, R.; Kiisk, M.; Persson, Per; Mattsson, Soeren; Thornberg, C.; Skog, G.

    2000-02-01

    The radionuclide 14 C is produced in all types of nuclear reactors mainly by neutron induced reactions in oxygen ( 17 O), nitrogen ( 14 N) and carbon ( 13 C). Part of the 14 C created is continuously released during normal operation as airborne effluents in various chemical forms (such as CO 2 , CO and hydrocarbons) to the surroundings. Because of the biological importance of carbon and the long physical half-life of 14 C, it is of interest to measure the releases and their incorporation into living material. The 14 C activity concentrations in annual tree rings and air around two Swedish nuclear power plants (Barsebaeck and Forsmark) as well as the background 14 C activity levels from two reference sites in southern Sweden during 1973-1996 are presented in this report. In order to verify the reliability of the method some investigations have been conducted at two foreign nuclear sites, Sellafield fuel reprocessing plant in England, and Pickering nuclear generating station in Canada, where the releases of 14 C are known to be substantial. Furthermore, results from some measurements in the vicinity of Paldiski submarine training centre in Estonia are presented. The results of the 14 C measurements of air, vegetation and annual tree rings around the two Swedish nuclear power plants show very low enhancements of 14 C, if at all above the uncertainty of the measurements. Even if the accuracy of the measurements of the annual tree rings is rather good (1-2%) the contribution of 14 C from the reactors to the environment is so small that it is difficult to separate it from the prevailing background levels of 14 C . This is the case for all sampling procedures: in air and vegetation as well as in annual tree rings. Only on a few occasions an actual increase is observed. However, although the calculations suffer from rather large uncertainties, the calculated release rate from Barsebaeck is in fair agreement with reported release data. The results of this investigation show

  1. Development of a C3-symmetric benzohydroxamate tripod: Trimetallic complexation with Fe(III), Cr(III) and Al(III)

    Science.gov (United States)

    Baral, Minati; Gupta, Amit; Kanungo, B. K.

    2016-06-01

    The design, synthesis and physicochemical characterization of a C3-symmetry Benzene-1,3,5-tricarbonylhydroxamate tripod, noted here as BTHA, are described. The chelator was built from a benzene as an anchor, symmetrically extended by three hydroxamate as ligating moieties, each bearing O, O donor sites. A combination of absorption spectrophotometry, potentiometry and theoretical investigations are used to explore the complexation behavior of the ligand with some trivalent metal ions: Fe(III), Cr(III), and Al(III). Three protonation constants were calculated for the ligand in a pH range of 2-11 in a highly aqueous medium (9:1 H2O: DMSO). A high rigidity in the molecular structure restricts the formation of 1:1 (M/L) metal encapsulation but shows a high binding efficiency for a 3:1 metal ligand stoichiometry giving formation constant (in β unit) 28.73, 26.13 and 19.69 for [M3L]; Mdbnd Fe(III), Al(III) and Cr(III) respectively, and may be considered as an efficient Fe-carrier. The spectrophotometric study reveals of interesting electronic transitions occurred during the complexation. BTHA exhibits a peak at 238 nm in acidic pH and with the increase of pH, a new peak appeared at 270 nm. A substantial shifting in both of the peaks in presence of the metal ions implicates a s coordination between ligand and metal ions. Moreover, complexation of BTHA with iron shows three distinct colors, violet, reddish orange and yellow in different pH, enables the ligand to be considered for the use as colorimetric sensor.

  2. ORIGIN OF PALMITIC ACID CARBON IN PALMITATES FORMED FROM HEXADECANE-1-C14 AND TETRADECANE-1-C14 BY MICROCOCCUS CERIFICANS

    Science.gov (United States)

    Finnerty, W. R.; Kallio, R. E.

    1964-01-01

    Finnerty, W. R. (University of Iowa, Iowa City), and R. E. Kallio. Origin of palmitic acid carbon in palmitates formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans. J. Bacteriol. 87:1261–1265. 1964.—Degradation of the palmitic acid moiety of cetyl palmitate and myristyl palmitate formed from hexadecane-1-C14 and tetradecane-1-C14 by Micrococcus cerificans was carried out. The patterns of C14 labeling in palmitic acid from cetyl palmitate showed that hexadecane is oxidized at the C1 position, and cetyl alcohol and palmitic acid thus formed are directly esterified. Palmitic acid arising from tetradecane and esterified to tetradecanol appeared to have been synthesized by the addition of two carbon atoms to an existing 14-carbon atom skeleton. Considerable mixing of C14 occurred in the C1 and C2 positions of palmitic acid thus synthesized. PMID:14188700

  3. Synthesis of 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole and 1-(4-sulfonamide-phenyl)-5-(4-fluoro-phenyl)-5-[14C]-1,2,3- triazole as novel carbon-14 anticonvulsant

    International Nuclear Information System (INIS)

    Saemian, N.; Shirvani, G.; Matloubi, H.

    2006-01-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole and 1-(4-sulfonamide-phenyl)-5-(4- fluoro-phenyl)-5-[ 14 C]-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-fluoro-benzonitrile-[cyano- 14 C]. (author)

  4. Dicty_cDB: FC-BS14 [Dicty_cDB

    Lifescience Database Archive (English)

    Full Text Available FC (Link to library) FC-BS14 (Link to dictyBase) - - - Contig-U16399-1 FC-BS14E (Li...nk to Original site) - - - - - - FC-BS14E 534 Show FC-BS14 Library FC (Link to library) Clone ID FC-BS14 (Li.../dictycdb.biol.tsukuba.ac.jp/CSM/FC/FC-BS/FC-BS14Q.Seq.d/ Representative seq. ID FC-BS...14E (Link to Original site) Representative DNA sequence >FC-BS14 (FC-BS14Q) /CSM/FC/FC-BS/FC-BS14Q.Seq.... vs CSM-cDNA Score E Sequences producing significant alignments: (bits) Value FC-BS14 (FC-BS

  5. NMR and TRLFS studies of Ln(iii) and An(iii) C5-BPP complexes† †Electronic supplementary information (ESI) available: LIFDI-MS spectra and additional NMR spectra. See DOI: 10.1039/c4sc03103b

    Science.gov (United States)

    Beele, Björn B.; Geist, Andreas; Müllich, Udo; Kaden, Peter; Panak, Petra J.

    2015-01-01

    C5-BPP is a highly efficient N-donor ligand for the separation of trivalent actinides, An(iii), from trivalent lanthanides, Ln(iii). The molecular origin of the selectivity of C5-BPP and many other N-donor ligands of the BTP-type is still not entirely understood. We present here the first NMR studies on C5-BPP Ln(iii) and An(iii) complexes. C5-BPP is synthesized with 10% 15N labeling and characterized by NMR and LIFDI-MS methods. 15N NMR spectroscopy gives a detailed insight into the bonding of C5-BPP with lanthanides and Am(iii) as a representative for trivalent actinide cations, revealing significant differences in 15N chemical shift for coordinating nitrogen atoms compared to Ln(iii) complexes. The temperature dependence of NMR chemical shifts observed for the Am(iii) complex indicates a weak paramagnetism. This as well as the observed large chemical shift for coordinating nitrogen atoms show that metal–ligand bonding in Am(C5-BPP)3 has a larger share of covalence than in lanthanide complexes, confirming earlier studies. The Am(C5-BPP)3 NMR sample is furthermore spiked with Cm(iii) and characterized by time-resolved laser fluorescence spectroscopy (TRLFS), yielding important information on the speciation of trace amounts of minor complex species. PMID:29560242

  6. Excitation functions of the systems 12C+14C and 13C+12C

    International Nuclear Information System (INIS)

    Haindl, E.

    1975-01-01

    The excitation functions of the systems 12 C+ 14 C and 13 C+ 12 C are investigated for different exit channels. The excitation functions measured do not show correlated structures as in the system 12 C+ 12 C. (WL/AK) [de

  7. Determination of 14CO2 in breath and 14C in stool after oral administration of cholyl-1-[14C]glycine: clinical application

    International Nuclear Information System (INIS)

    Roda, A.; Roda, E.; Aldini, R.; Mazzella, G.; Festi, D.; Sama, C.; Barbara, L.

    1977-01-01

    Twenty patients with intestinal bacterial overgrowth and 20 control subjects were investigated for bile acid deconjugation, by measuring 14 CO 2 in the breath after cholyl-1-[ 14 C]glycine administration. 14 CO 2 output/24 h was 11.0 +- 5.2% (mean +- SD) in controls and 54.2 +- 14.0% (mean +- SD) in bacterial-overgrowth patients (P 14 CO 2 excretion rate in 12 h, when normalized to 100% of the dose at the 12th hour, gave an even finer discrimination between the two groups (no false responses). 14 C in stool, analyzed in 20 malabsorption patients and 20 controls by two different techniques, was 6.6 +- 4% and 31.38 +- 20.7% (mean +- SD), respectively. Results by the two different techniques described here correlated well (r = 0.99). Bile acid malabsorption was in reasonable agreement (r = 0.67) with percentage of ''chenoid'' (chenodeoxycholic acid plus ursodeoxycholic acid) in the stool by gas-liquid chromatography; a poorer correlation was observed when ''choloid'' (cholic acid plus its epimers) were plotted vs. 14 C in stool

  8. The production of (14C) oxalate during the metabolism of (14C) carbohydrates in isolated rat hepatocytes.

    Science.gov (United States)

    Rofe, A M; James, H M; Bais, R; Edwards, J B; Conyers, R A

    1980-04-01

    Oxalate (14C) was produced during the metabolism of (U-14C) carbohydrates in hepatocytes isolated from normal rats. At 10 mM, the order of oxalate production was fructose > glycerol > xylitol > sorbitol greater than or equal to glucose in the ratio 10 : 4 : 3 : 1 : 1. This difference between oxalate production from fructose and glucose was reflected in their rates of utilisation, glucose being poorly metabolised in hepatocytes from fasted rats. Fructose was rapidly metabolised, producing glucose, lactate and pyruvate as the major metabolites. Glycerol, xylitol and sorbitol were metabolised at half the rate of fructose, the major metabolites being glucose, lactate and glycerophosphate. The marked similarity in the pattern of intermediary metabolites produced by these polyols was not, however, reflected in the rates of oxalate production. Hepatic polyol metabolism resulted in high levels of cytosolic NADH, as indicated by elevated lactate : pyruvate and glycerophosphate : dihydroxyacetone phosphate ratios. The artificial electron acceptor, phenazine methosulphate (PMS) stimulated oxalate production from the polyols, particularly xylitol. In the presence of PMS, the order of oxalate production was fructose greater than or equal to xylitol > glycerol > sorbitol in the ratio 10 : 10 : 6 : 2. The production of glucose, lactate and pyruvate from the polyols was also stimulated by PMS, whereas the general metabolism of fructose, including oxalate production, was little affected. Oxalate (14C) was produced from (1-14C), (2-14C) and (6-14C) but not (3,4-14C) glucose in hepatocytes isolated from non-fasted, pyridoxine-deficient rats. Whilst this labelling pattern is consistent with oxalate being produced by a number of pathways, it is suggested that metabolism via hydroxypyruvate is a major route for oxalate production from various carbohydrates, with perhaps the exception of xylitol, which appears to have an alternative mechanism for oxalate production. The observation that

  9. Incorporation of 14C-succinate in Synechococcus

    International Nuclear Information System (INIS)

    Doehler, G.

    1983-01-01

    The cyanobacterium Synechococcus (= Anacystis nidulans) was grown under normal air conditions (0.03 vol.% CO 2 ) and in low white light (0.5 x 10 3 μW/cm 2 ) at 37 0 C. Kinetics of 14 C incorporation into several soluble products and pigments were studied after adding 14 C-succinate during photosynthesis and in the dark using the autoradiographic method. Radioactivity was found mainly in glutamate and aspartate during the photosynthetic period independent on 3-(3',4'-dichlorphenyl)-1,1-dimethylurea preincubation. In the dark period 14 C label could also be detected in malate. Short-term kinetics experiments showed a decrease in 14 C label of glutamate and a parallel increase of aspartate. Results were discussed in respect to the interrupted tricarboxylic acid cycle. (author)

  10. Reactions of saccharides catalyzed by molybdate ions. XXXIII. Use of. cap alpha. (U-/sup 14/C)glucan for preparation of /sup 14/C-labelled saccharides

    Energy Technology Data Exchange (ETDEWEB)

    Bilik, V; Biely, P [Institute of Chemistry, Centre for Chemical Research, Slovak Academy of Sciences, Bratislava (Czechoslovakia); Kolina, J [Ustav pro Vyzkum, Vyrobu a Vyuziti Radioisotopu, Prague (Czechoslovakia)

    1984-01-01

    D-(U-/sup 14/C)glucose obtained in acid hydrolysis of ..cap alpha..-(U-/sup 14/C)glucan (2 M-HCl) was epimerized under a catalytic action of molybdate ions to D-(U-/sup 14/C)mannose isolated with a 20% yield. Oxidative degradation of 4-nitrophenylhydrazones of D-(U-/sup 14/C)arabinose and D-(U-/sup 14/C)xylose resulted in D-(U-/sup 14/C)erythrose and D-(U-/sup 14/C)threose, respectively, with a 15% yield relative to the starting aldopentoses. Nitromethane synthesis with D-(U-/sup 14/C)lyxose followed by oxidative decomposition of the corresponding nitrohexitols yielded /sup 14/C-labelled D-galactose. Described is also the preparation of D-(U-/sup 14/C)arabinose from D-(U-/sup 14/C)glucose and the conversion of D-(U-/sup 14/C)arabinose to D-(U-/sup 14/C)xylose and D-(U-/sup 14/C)lyxose.

  11. Pyrroloindolone synthesis via a Cp*Co(III)-catalyzed redox-neutral directed C-H alkenylation/annulation sequence.

    Science.gov (United States)

    Ikemoto, Hideya; Yoshino, Tatsuhiko; Sakata, Ken; Matsunaga, Shigeki; Kanai, Motomu

    2014-04-09

    A unique synthetic utility of a Cp*Co(III) catalyst in comparison with related Cp*Rh(III) catalysts is described. A C2-selective indole alkenylation/annulation sequence proceeded smoothly with catalytic amount of a [Cp*Co(III)(C6H6)](PF6)2 complex and KOAc. Intramolecular addition of an alkenyl-Cp*Co species to a carbamoyl moiety gave pyrroloindolones in 58-89% yield in one pot. Clear difference was observed between the catalytic activity of the Cp*Co(III) complex and those of Cp*Rh(III) complexes, highlighting the unique nucleophilic activity of the organocobalt species. The Cp*Co(III) catalysis was also suitable for simple alkenylation process of N-carbamoyl indoles, and broad range of alkynes, including terminal alkynes, were applicable to give C2-alkenylated indoles in 50-99% yield. Mechanistic studies on C-H activation step under Cp*Co(III) catalysis with the aid of an acetate unit as well as evaluation of the difference between organo-Co(III) species and organo-Rh(III) species are also described.

  12. 14C Behaviour in PWR coolant

    International Nuclear Information System (INIS)

    Sims, Howard; Dickinson Shirley; Garbett, Keith

    2012-09-01

    Although 14 C is produced in relatively small amounts in PWR coolant, it is important to know its fate, for example whether it is released by gaseous discharge, removed by absorption on ion exchange (IX) resins or deposited on the fuel pin surfaces. 14 C can exist in a range of possible chemical forms: inorganic carbon compounds (probably mainly CO 2 ), elemental carbon, and organic compounds such as hydrocarbons. This paper presents results from a preliminary survey of the possible reactions of 14 C in PWR coolant. The main conclusions of the study are: - A combination of thermal and radiolytic reactions controls the chemistry of 14 C in reactor coolant. A simple chemical kinetic model predicts that CH 3 OH would be the initial product from radiolytic reactions of 14 C following its formation from 17 O. CH 3 OH is predicted to arise as a result of reactions of OH . with CH 4 and CH 3 , and it persists because there is no known radiation chemical reduction mechanism. - Thermodynamic considerations show that CH 3 OH can be thermally reduced to CH 4 in PWR conditions, although formation of CO 2 from small organics is the most thermodynamically favourable outcome. Such reactions could be catalysed on active nickel surfaces in the primary circuit. - Limited plant data would suggest that CH 4 is the dominant form in PWR and CO 2 in BWR. This implies that radiation chemistry may be important in determining the speciation. - Addition of acetate does not affect the amount of 14 C formed, but the addition of large amounts of stable carbon would lead to a large range of additional products, some of which would be expected to deposit on fuel pin surfaces as high molecular weight hydrocarbons. However, the subsequent thermal decomposition reactions of these products are not known. - Acetate addition may represent a small input of 12 C compared with organic material released from CVCS resins, although the importance of this may depend on whether that is predominantly soluble

  13. Synthesis of (/sup 14/C)Zolpidem

    Energy Technology Data Exchange (ETDEWEB)

    Allen, J.; Tizot, A.

    1986-04-01

    The synthesis of (/sup 14/C)Zolpidem, a new hypnotic agent having a non-benzodiazepine structure, is described. This compound was synthesised in a 64% overall radiochemical yield from potassium (/sup 14/C)cyanide and with a specific radioactivity of 56 mCi/mmol. It was used for pharmacokinetic and drug metabolism studies.

  14. Transformation of the herbicide [14C]glufosinate in soils

    International Nuclear Information System (INIS)

    Smith, A.E.

    1989-01-01

    The degradation of 2 μg/g [ 14 C]glufosinate (DL-homoalan-4-ylmethylphosphinic acid) was studied in clay, clay loam, and sandy loam soils at 85% field capacity and at 20 degree C. Over a 4-week period the soils were extracted and analyzed for transformation products by radiochemical and gas chromatographic techniques. In all soils there was release of [ 14 C]carbon dioxide and formation of [ 14 C]-3-(hydroxymethylphosphinyl)propionic acid (MPPA) as major degradation products. Within 21 days, about 55% of the applied 14 C herbicide had been transformed to MPPA in the sandy loam and 19% to [ 14 C]carbon dioxide. After 28 days, approximately 45% of the 14 C herbicide had been transformed to MPPA in the clay and clay loam and 10% released as [ 14 C]carbon dioxide. At all samplings, other 14 C transformation products appeared to be insignificant

  15. Accelerator mass spectrometry analysis of 14C-oxaliplatin concentrations in biological samples and 14C contents in biological samples and antineoplastic agents

    Science.gov (United States)

    Toyoguchi, Teiko; Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi; Kato, Kazuhiro; Tokanai, Fuyuki

    2015-10-01

    Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the 14C concentration in 14C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) - AMS system. The calibration curves of 14C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a 14C content of water in three vacuum blood collection tubes and a syringe were measured. 14C was not detected from water in these devices. The mean 14C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of 14C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, 14C contents of the antineoplastic agents were quantitated. 14C contents were different among 10 antineoplastic agents; 14C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

  16. Appraisal of the /sup 14/C-glycocholate acid test with special reference to the measurement of faecal /sup 14/C excretion

    Energy Technology Data Exchange (ETDEWEB)

    Scarpello, J H.B.; Sladen, G E [Royal Hospital, Sheffield (UK). Academic Div. of Medicine

    1977-09-01

    The /sup 14/C-glycocholate test, including the measurement of marker corrected faecal /sup 14/C, has been assessed in the following groups of subjects: normal controls (18), patients with diarrhoea not attributable to altered bile acid metabolism (21), patients with diverticula of the small intestine (12), patients with previous resection of ileum and often proximal colon (34), and established ileostomists (10). Patients with diverticular disease had increased breath /sup 14/CO/sub 2/ excretion, but normal faecal excretion of /sup 14/C, and this test was more frequently abnormal than the Schilling test. Ileostomists excreted increased amounts of faecal /sup 14/C, even when the ileum was intact and apparently normal. The pattern after resection was complex. Breath /sup 14/C output was normal if the ileal resection was less than 25 cm in length, although some of these patients had increased faecal /sup 14/C excretion if, in addition, at least 15 cm of proximal colon had been resected or by-passed. Longer ileal resections were associated with increased breath and/or faecal /sup 14/C excretion, depending in part on the length of colon resected or by-passed and the 24 hour faecal volume. Fewer than half these patients had both increased breath and faecal excretion of isotope and faecal /sup 14/C alone was occasionally normal with an ileal resection of 50 cm or more. The /sup 14/C-glycocholate test was more frequently abnormal than the Schilling test in this group. The use of faecal marker correction had only a minor impact on the results. These data suggest that, in patients with ileal resection, faecal /sup 14/C, like faecal weight, is determined by the extent of colonic resection as well as by the amount of ileum resected.

  17. Synthesis of (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolic acid, methyl (1'-/sup 13/C)olivetolate and (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolic acid

    Energy Technology Data Exchange (ETDEWEB)

    Porwoll, J P; Leete, E [Minnesota Univ., Minneapolis (USA). Dept. of Chemistry

    1985-03-01

    Potential advanced intermediates in the biosynthesis of delta/sup 9/-tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous /sup 13/C atoms and /sup 14/C. Methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolate was prepared from lithium (/sup 13/C/sub 2/)acetylide and dimethyl (2-/sup 14/C)malonate. Reaction with geranyl bromide afforded methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The /sup 13/C-/sup 13/C couplings observable in the /sup 13/C NMR spectra of these /sup 13/C-enriched compounds and their synthetic precursors are recorded. Methyl (1'-/sup 14/C)olivetolate was prepared from /sup 13/CO/sub 2/ to confirm assignments of the /sup 13/C chemical shifts in the pentyl side chain of these compounds.

  18. Thermodynamic and kinetic studies of the equilibration reaction between the sulfur and carbon bonded forms of a cobalt(III) complex with the ligands 1,4,7-triazycyclononane and 1,4-diaza-7-thiacyclodecane

    DEFF Research Database (Denmark)

    Song, Y.S.; Becker, J.; Kofod, Pauli

    1996-01-01

    The new cyclic thioether 1,4-diaza-7-thiacyclodecane, dathicd, has been synthesized and used for the prepn. of the sulfur- and carbon-bonded cobalt(III) complexes: [Co(tacn)(S-dathicd)]Cl3.5H2O and [Co(tacn)(C-dathicd)](ClO4)2 (tacn, 1,4,7-triazacyclononane; C-dathicd, 1,4-diamino-7-thiacyclodecan......-sulfur complex to form the alkyl complex gave 100% loss of deuterium. It is concluded that the labile methylene proton is bound to the carbon atom which in the alkyl complex is bound to cobalt(III). From the kinetic data it is estd. that the carbanion reacts with water 270 times faster than it is captured...

  19. European dendrochronoloy and C-14 dating of timber

    International Nuclear Information System (INIS)

    Fletcher, J.M.

    1975-01-01

    An account is given of the development of dendrochronology and C-14 dating in Europe. Corrections to raw C-14 dates, sampling and the uncertainty of C-14 ages of wood, and correlation of dates obtained by the two methods, are discussed. (U.K.)

  20. Synthesis of 14C-labeled stepholidine

    International Nuclear Information System (INIS)

    Yang Liu; Zhang Xin

    1988-01-01

    L-Tetrahydroprotoberberine (THPB) alkaloids are dopamine-receptor antagonists. Stepholidine has been shown to possess the strongest pharmacological effects among the THPB alkaloids studied. In order to study its metabolism and the mode of action of the drug, a radiolabeled stepholidine was required. We report here the synthesis of 14 C-labeled stepholidine by Mannich condensation of 7-benzyloxy-1-(4-benzyloxy-3-hydroxy-benzyl)-6-methoxy-1,2,3,4-tetrahydroisoquinoline with ( 14 C)formaldehyde followed by methylation and debensylation in 32% radiochemical yield. (author)

  1. Synthesis of /sup 14/C-labelled milrinone

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, D.R.; Johnston, D.; Andrews, R.S. (Stirling-Winthrop, Alnwick (UK). Research and Development Div.)

    1985-02-01

    A synthetic procedure for producing /sup 14/C-labelled milrinone, a potent new cardiotonic agent, is described. The synthesis was achieved in two steps from 1-(4-pyridyl)propan-2-one utilising (2-/sup 14/C)cyanoacetamide as the source of the radiolabel. The overall chemical yield was 46% and the radiochemical yield 35%.

  2. The DSS-14 C-band exciter

    Science.gov (United States)

    Rowan, D. R.

    1989-01-01

    The development and implementation of a C-band exciter for use with the Block IV Receiver-Exciter Subsystem at Deep Space Station 14 (DSS-14) has been completed. The exciter supplements the standard capabilities of the Block IV system by providing a drive signal for the C-band transmitter while generating coherent translation frequencies for C-band (5-GHz) to S-band (2.2- to 2.3-GHz) Doppler extraction, C-band to L-band (1.6-GHz) zero delay measurements, and a level calibrated L-band test signal. Exciter functions are described, and a general explanation and description of the C-band uplink controller is presented.

  3. Effect of level of dietary protein on the distribution of 14C-activity from exogenous 14C-inosine in chicks

    International Nuclear Information System (INIS)

    Masushige, Shoichi; Tadokoro, Tadahiro; Suzuki, Takao; Nakajima, Hisao.

    1983-01-01

    The effect of dietary protein level on the metabolic fate of intraperitoneally administered (exogeneous) 8- 14 C-inosine in chicks was studied. Three different protein level diets (low, standard and high) were prepared. Chicks were fed on these diets for 10 days, respectively and the following results were found: (1) RNA content of liver, small intestine and muscle in chicks fed on a low protein diet was decreased as compared to other diet groups, but no difference was observed in kidney or pancreas. (2) 14 C uptake by organs from exogeneous 8- 14 C-inosine was determined. The uptake of 14 C in kidney, pancreas and small intestine was higher than that in liver and muscle. Moreover, the uptake by tissues in the low protein groups was significantly higher than that in either the standard or high protein groups, but no difference was observed between these latter two groups. (3) The rate of incorporation of 14 C labelled purine by acid soluble materials and RNA was higher in kidney, pancreas and small intestine than in liver and muscle, and also higher in chicks fed on a low protein diet than in either the standard or high protein groups. (4) It was revealed that the 14 C-labelled purine rings from 8- 14 C-inosine were incorporated into AMP and GMP as constituents of RNA. (author)

  4. Carbohydrate distribution and 14C-photosynthates uptake in the curved fruits of cucumber

    Energy Technology Data Exchange (ETDEWEB)

    Kanahama, K. [Yamagata univ., Tsuruoka (Japan); Saito, T.

    1988-12-15

    The major carbohydrates in cucumber fruit were reducing sugars, which increased to the highest concentration of about 2.0% of fresh weight at harvest for fresh fruit, that is, 6-8 days after flowering and 73-116g in fresh weight. Starch was highest in concentration at flowering although it was negligible as compared with sugars. Reducing sugar concentration was higher in the core (septum and placenta) than in the flesh (receptacle and pericarp). Moreover, it was higher outside than inside the curvature at the curvature increasing stage, while the reverse was true at the curvature decreasing stage. Labelled carbon was fed to the single leaf on the same node as the fruit. Twenty hours after feeding, {sup 14}C-activity was higher in carpel II (outside the curvature and opposite to the tendril) than in carpels I (facing the stem) and III (inside the curvature and facing the tendril) when fed at the curvature increasing stage. When fed at the curvature decreasing stage after the curvature maximum stage had been attained, {sup 14}C-activity was higher in carpel III than in carpels I and II. From these results, it was suggested that the curvature of cucumber fruit occurred due to the competition among the carpels, in uptake of carbohydrates under limited photosynthesis. Each carpel is presumed to be different in sink activity according to its congenital developmental order and stages. Differential carbohydrate translocation due to localization of vascular bundle connections between leaves and fruit is improbable.

  5. Structure of 14C and 14B from the C,1514(d ,3He)B,1413 reactions

    Science.gov (United States)

    Bedoor, S.; Wuosmaa, A. H.; Albers, M.; Alcorta, M.; Almaraz-Calderon, Sergio; Back, B. B.; Bertone, P. F.; Deibel, C. M.; Hoffman, C. R.; Lighthall, J. C.; Marley, S. T.; Mcneel, D. G.; Pardo, R. C.; Rehm, K. E.; Schiffer, J. P.; Shetty, D. V.

    2016-04-01

    We have studied the C,1514(d ,3He)B,1413 proton-removing reactions in inverse kinematics. The (d ,3He ) reaction probes the proton occupation of the target ground state, and also provides spectroscopic information about the final states in B,1413. The experiments were performed using C,1514 beams from the ATLAS accelerator at Argonne National Laboratory. The reaction products were analyzed with the HELIOS device. Angular distributions were obtained for transitions from both reactions. The 14C-beam data reveal transitions to excited states in 13B that suggest configurations with protons outside the π (0 p3 /2) orbital, and some possibility of proton cross-shell 0 p -1 s 0 d excitations, in the 14C ground state. The 15C-beam data confirm the existence of a broad 2- excited state in 14B. The experimental data are compared to the results of shell-model calculations.

  6. Synthesis of 1-benzyl-4-[(5,6-dimethoxy[2-14C]-1-indanon)-2-YL]-methylpiperidine hydrochloride (E2020-14C)

    International Nuclear Information System (INIS)

    Iimura, Youichi; Mishima, Mannen; Sugimoto, Hachiro

    1989-01-01

    1-Benzyl-4-[(5,6-dimethoxy[2- 14 C]-1-indanon)-2-yl]-methylpiperidine hydrochloride (E2020- 14 C), and acetylcholinesterase inhibitor for studying the pharmacokinetic profiles of E2020, was synthesized from 5,6-dimethoxy[2- 14 C]-1-indanone as the labelled starting material. (author)

  7. Calibration of 14C Histograms : A Comparison of Methods

    NARCIS (Netherlands)

    Stolk, Ad; Törnqvist, Torbjörn E.; Hekhuis, Kilian P.V.; Berendsen, Henk J.A.; Plicht, Johannes van der

    1994-01-01

    The interpretation of C-14 histograms is complicated by the non-linearity of the C-14 time scale in terms of Calendar years, which may result in clustering of C-14 ages in certain time intervals unrelated to the (geologic or archaeologic) phenomenon of interest. One can calibrate C-14 histograms for

  8. Formation and bio release of bound residues of [14 C]-lindane and [14 C]-parathion in two Brazilian soils

    International Nuclear Information System (INIS)

    Andrea, M.M. de.

    1992-01-01

    This work studied the extractable and bound residues formation of 14 C-lindane and 14 C-parathion immediately after application and after 3 months of interaction of the pesticides with the soils. Metabolism, bio release, and the possible bioavailability of bound residues were studied by employing bio meter flasks which allowed a relative comparison of the behaviour of the two different 14 C-pesticides, by a balance of the applied or present radiocarbon in the soils after the bio tests. (author)

  9. Synthesis of (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolic acid, methyl (1'-/sup 13/C)olivetolate and (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolic acid

    Energy Technology Data Exchange (ETDEWEB)

    Porwoll, J.P.; Leete, E. (Minnesota Univ., Minneapolis (USA). Dept. of Chemistry)

    1985-03-01

    Potential advanced intermediates in the biosynthesis of delta/sup 9/-tetrahydrocannabinol, the major psychoactive principle of marijuana, have been synthesized labeled with two contiguous /sup 13/C atoms and /sup 14/C. Methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)olivetolate was prepared from lithium (/sup 13/C/sub 2/)acetylide and dimethyl (2-/sup 14/C)malonate. Reaction with geranyl bromide afforded methyl (5,6-/sup 13/C/sub 2/, 1-/sup 14/C)cannabigerolate, and hydrolysis of these methyl esters with lithium propyl mercaptide yielded the corresponding labeled acids. The /sup 13/C-/sup 13/C couplings observable in the /sup 13/C NMR spectra of these /sup 13/C-enriched compounds and their synthetic precursors are recorded. Methyl (1'-/sup 14/C)olivetolate was prepared from /sup 13/CO/sub 2/ to confirm assignments of the /sup 13/C chemical shifts in the pentyl side chain of these compounds.

  10. {sup 14}C emission from Swedish nuclear power plants and its effect on the {sup 14}C levels in the environment

    Energy Technology Data Exchange (ETDEWEB)

    Stenstroem, K.; Erlandsson, Bengt; Hellborg, R.; Kiisk, M.; Persson, Per [Lund Univ. (Sweden). Dept. of Nuclear Physics; Mattsson, Soeren; Thornberg, C. [Lund Univ., Malmoe (Sweden). Dept. of Radiation Physics; Skog, G. [Lund Univ. (Sweden). Dept. of Quaternary Geology

    2000-02-15

    The radionuclide {sup 14}C is produced in all types of nuclear reactors mainly by neutron induced reactions in oxygen ({sup 17}O), nitrogen ({sup 14}N) and carbon ({sup 13}C). Part of the {sup 14}C created is continuously released during normal operation as airborne effluents in various chemical forms (such as CO{sub 2}, CO and hydrocarbons) to the surroundings. Because of the biological importance of carbon and the long physical half-life of {sup 14}C, it is of interest to measure the releases and their incorporation into living material. The {sup 14}C activity concentrations in annual tree rings and air around two Swedish nuclear power plants (Barsebaeck and Forsmark) as well as the background {sup 14}C activity levels from two reference sites in southern Sweden during 1973-1996 are presented in this report. In order to verify the reliability of the method some investigations have been conducted at two foreign nuclear sites, Sellafield fuel reprocessing plant in England, and Pickering nuclear generating station in Canada, where the releases of {sup 14}C are known to be substantial. Furthermore, results from some measurements in the vicinity of Paldiski submarine training centre in Estonia are presented. The results of the {sup 14}C measurements of air, vegetation and annual tree rings around the two Swedish nuclear power plants show very low enhancements of {sup 14}C, if at all above the uncertainty of the measurements. Even if the accuracy of the measurements of the annual tree rings is rather good (1-2%) the contribution of {sup 14}C from the reactors to the environment is so small that it is difficult to separate it from the prevailing background levels of {sup 14}C . This is the case for all sampling procedures: in air and vegetation as well as in annual tree rings. Only on a few occasions an actual increase is observed. However, although the calculations suffer from rather large uncertainties, the calculated release rate from Barsebaeck is in fair agreement

  11. How accurate is the 14C method

    International Nuclear Information System (INIS)

    Nydal, R.

    1979-01-01

    Radiocarbon daters have in recent years focussed their interest on accuracy and reliability of 14 C dates. The use of dates for resolving fine chronological structures that are not dateable otherwise has stressed this point. The total uncertainty in dating an event is composed of errors relating to dating of the sample, i.e. uncertainty in measured quantities, deviations from assumed content of 14 C in material when alive; and errors related to quality of sample material, i.e. contamination from carbon of different age, diffuse context between sample and event. Statistical variability in counting of 14 C activity gives the most important contribution to measurement uncertainty - increasing with age and shortage of sample material. Corrections for isotopic fractionation and reservoir effects must be performed, and - most important when dates are compared with historical ages - the dendrochronological calibration will correct for past variations in the atmospheric 14 C content. Future improvement of dating precision can however only be obtained by the combined efforts of both daters and submitters of samples, thus minimizing errors related to selection and handling of sample material as well as those related to the 14 C method and measurements. (Auth.)

  12. Clinical investigation of 14C-urea breath test

    International Nuclear Information System (INIS)

    Yu Yongli; Zhu Ruisen; Ji Hong; Luo Quanyong

    2000-01-01

    To investigate clinical value of 14 C-urea breath test ( 14 C-UBT) for the diagnosis of Helicobacter pylori(Hp), 70 patients were both performed gastroscopy (taking gastric mucosae biopsy for rapid urease test and histology) and 14 C-UBT (some patients by Hp-IgG or DNAHp test also) within two days. The positive cases of both rapid urease test and histology was defined as 'gold standard' of Hp-positive, whereas the negative cases of both rapid urease test and histology as 'gold standard' of Hp-negative. The sensitivity of 14 C-UBT was 93.2%, the specificity 73.1%, and the diagnostic accuracy 85.7%. The difference (comparing with 'gold standard') was not marked (x 2 = 0.9 0.05(1) 2 = 3.84, P>0.05). But the diagnostic accuracy of 14 C-UBT (85.7%) and Hp-IgG (50%) had a marked difference (x 2 13.80>x 0.01(1) 2 = 6.64, P 14 C-UBT was easy to operate, reliable and suitable for clinical application

  13. Medición del flujo de neutrinos cósmicos ultra energéticos mediante detectores de superficie

    OpenAIRE

    Pieroni, Pablo Emanuel

    2016-01-01

    Esta Tesis estudia la medición de neutrinos cósmicos ultra energéticos mediante detectores de superficie. Básicamente existen dos mecanismos a través de los cuales los neutrinos en el rango del EeV pueden inducir señales distinguibles a nivel de superficie. El primero consiste en la interacción de un neutrino en la atmósfera, via corrientes cargadas o neutras, y la subsiguiente producción de una cascada atmosférica extendida descendente. El segundo se basa en la interacción de un neutrino tau...

  14. Application of the subchannel analysis code COBRA III C for liquid sodium

    International Nuclear Information System (INIS)

    Nissen, K.L.

    1981-01-01

    The subchannel-analysis code COBRA III C was developed to gain knowledge of mass flow and temperature distribution in rod bundles of light water reactors. A comparison of experimental results for the temperature distribution in a 19 rod bundle with calculations done by the computer program shows the capability of COBRA III C to handle liquid sodium cooling. The code needs sodium properties as well as changed correlations for turbulent mixing and heat transfer at the rod. (orig.) [de

  15. Fate of 14C-labelled compounds in marine environment

    International Nuclear Information System (INIS)

    Kale, S.P.; Raghu, K.; Sherkhane, P.D.; Murthy, N.B.K.

    1999-01-01

    Model ecosystems have played an important role in predicting environmental behavior of agrochemicals. The microcosms used in these studies generally include soil units containing usual biotic components common for that ecosystem. In present studies, scope of two such ecosystems has been extended to study the fate of 14 C-labelled pesticides in marine environment. 14 C-labelled pesticides used in these studies were chlorpyrifos, DDT and HCH. Two systems were developed in laboratory simulating marine environment to study the fate of these pesticides. The first system was developed in an all glass aquarium tank with marine sediments, seawater, clams and algae and is referred to as marine ecosystem. The second system was developed to permit the total 14 C-mass balance studies. It contained marine sediments under moist (60% water holding capacity) or flooded conditions and it is referred to as continuous flow system. Fate of 14 C-DDT was studied in marine ecosystem while degradation of 14 C-chlorpyrifos and 14 C-HCH was studied in continuous flow system. 14 C-DDT did not bioaccumulate in clams while at the end of 60 days 50% of the applied 14 C-activity was present in sediment fraction of marine ecosystem. 14 C-HCH degradation showed about 22-26% mineralization while 45-55% of the applied activity was recovered as organic volatiles. No significant bound residues were formed. 14 C-chorpyrifos underwent considerable degradation in marine environment. TCP was the major degradation product. (author)

  16. Radioactive waste with 14C in Argentina

    International Nuclear Information System (INIS)

    Di Lello, D.S.

    2009-01-01

    14 C is a long half-life radioisotope, which is present in radioactive waste generated during the operation and decommissioning of nuclear power plants. 14 C can also be found in waste generated by medical diagnostic laboratories or any one generated by fields that deal with research and development (mainly connected with the biochemists area). According to international precedents the disposal of 14 C based on the final amount found in radioactive waste and its chemical form have conditioned the design and operation of the facilities (either because of the amount of it or the chemical form in which 14 C was present). We have to take into account that the design of facilities for radioactive waste disposal is included among the obligations of the National Radioactive Waste Management Program (PNGRR). It is absolutely necessary to count with enough information about the characteristics of any waste containing 14 C that is generated in Argentina, in order to be able to fulfil the requirements previously mentioned. The main characteristics of interest in the frame of the present project are: a) the principal reactions that take place for the formation of 14 C; b) The specific concentration of activity in materials where this radio nuclei is formed or is accumulated; c) To know which is the current step in the process of managing these wastes (in Argentina and all over the world). Either if it refers to bulk or conditioned storage, inside the generating facility; d) Transportation possibilities of 14 C under these conditions; e) The accumulated volume and the generation rate of this kind of waste in Argentina. This paper presents an initial collection and evaluation of the information related to the characteristics already mentioned, having gathered published material from the literature and information in the PNGRR up to this moment. The description of the characteristics of the radioactive waste containing 14 C from nuclear power plants, hospitals and research and

  17. Studies on dissipation and degradation of 14 C-DDT and 14 C-parathion in egyptian soil under field conditions

    International Nuclear Information System (INIS)

    Ezz El-Arab, A.; Mostafa, I.Y.

    1991-01-01

    The rates of dissipation and degradation of the insecticides DDT and parathion were studied under field conditionsm using 14 C-labelled chemicals. Over a period of 12 weeks, extractable, soil-bound and total 14 C-activity were recorded. In case of DDT, dissipation of 14 C-activity from soil showed a continuous and gradual increase reaching about 30% after 8 weeks and remained constant up to 12 weeks. The formation of DDE as a principal metabolite seems to be increasing with time ans accounted for approximately 25% of the extractable residues after 12 weeks. There was also a gradual significant increase in the formation of soil 14 C-bound residues which reached 12% of the total residues after the same period. On the other hand, parathion dissipation from the soil under the same conditions did not exceed 10% up to 12 weeks. The amount of 14 C-bound residues was found to contribute 33% of the applied dose. Analysis of the extractable fraction revealed that parathion was partly degraded by soil microorganisms into p-amino phenol, p-nitrophenol, paraoxon, amino parathion and aminoparaoxon in different percentages depending on the depth of soil. 2 fig.,1 tab

  18. 14C Carbofuran residue in rice-fish ecosystem model

    International Nuclear Information System (INIS)

    Sumatra, M.; Soekarna, D.; Suhanda; Kuswadi, A.N.

    1988-01-01

    14-C-carbofuran in the form of 14-C-Furada 3G was applied with doses of 0, 2, and 4 g/m2 to a rice-fish ecosystem model consisting of water, soil, rice, plant, and fish (Cyprinus carpio) in tanks of the size 1 m length, 1 m width, and 0.5 m depth. 14-C-carbofuran was released from 14-C-Furadan 3G, entered into the water, absorbed by plant root, and then distributed into the whole plant. A part of the 14-C-carbofuran was absorbed and retained by soil. In both doses of 4 and 2 g/m2, the 14-C-Furadan 3G was toxic to Cyprinus carpio under this experiment condition. (author). 5 refs, 5 figs, 6 tabs

  19. 14C-Methylenebisphenylisocyanate (14C-MDI). Study of absorption after single dermal and intradermal administration in rats

    International Nuclear Information System (INIS)

    Leibold, E.; Hoffmann, H.D.; Hildebrand, B.

    1999-01-01

    The absorption, distribution and excretion of radioactivity was studied in groups of four male Wistar rats following a single dermal and intradermal administration of 14 C- Methylenebisphenylisocyanate ( 14 C-MDI) at nominal dose levels of 4.0 and 0.4 mg/cm 2 for dermal administration and 0.4 mg/animal for intradermal administration. These dose levels nominally corresponded to 40 and 4.0 mg/animal for dermal administration. Considering the animal weights, dose levels corresponded to about 140 and 14 mg/kg body weight (dermal administration) and 1.4 mg/kg body weight (intradermal administration). In the experiments with dermal administration, animals were exposed for 8 hours and sacrificed 8, 24 or 120 h after beginning of exposure. In the experiment with intradermal administration, animals were sacrificed 120 h after treatment. After dermal administration of 14 C-MDI, mean recoveries of radioactivity from all dose groups were in the range from 97.86 to 108.07% of the total radioactivity administered. Generally, the largest proportion of radioactivity was found at the application site and dressing. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) increased with increasing sacrifice time. Dermal absorption was very low and quantitatively similar at both dose levels; maximally ca. 0.9 % of the applied radioactivity was absorbed. After intradermal administration of 14 C-MDI, the mean recovery of radioactivity was 100.90 % of the radioactivity administered. The largest proportion of radioactivity was found at the application site. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) amounted to about 26 % of the radioactivity applied. Irrespective of the mode of administration of 1 4C -MDI, concentrations of radioactivity in tissues and organs generally were below 1 μg Eq/g at 120 h after administration. In summary, the results of this study comparing systemic

  20. Application of AMS 14C measurements to criminal investigations

    International Nuclear Information System (INIS)

    Nakamura, T.; Ohta, T.; Nishida, M.; Rakowski, A.; Ikeda, A.; Oda, H.; Kojima, S.

    2007-01-01

    14 C variations of atmospheric CO 2 as well as carbonaceous fraction of living materials, such as collagen from tooth and bone, tissue, skin, hair, nail, etc., of modern humans are influenced by 14 C produced artificially by nuclear bomb tests in the atmosphere from late 1950s to early 1960s. By careful investigation of 14 C concentration of tree rings and human body samples formed in this time intervals, we can establish a relationship of their 14 C concentrations with calendar year. By applying this relation to a sample whose 14 C concentration can be measured, we can estimate the formation age of the sample. In addition, sources of the chemicals that were used in some criminal cases can be possibly identified, by their carbon isotope ratios ( 13 C/ 12 C and 14 C/ 12 C). This method of age determination has been applied to a forensic study, i.e., two criminal cases of murder. For each case, by comparing the measured 14 C abundances of several pieces of hair and one tooth (the third molar) from the body with the annual change on concentrations of bomb-produced 14 C, the time of death of the body and the age of the victim were estimated. The estimated values were consistent with the real ones that were revealed by the confession of the real murderers. (author)

  1. {8-14C}-Adenine and {1-14C}-isopentenyl pyrophosphate - precursors for root-produced cytokinins in the tomato (Lycopersicon esculentum mill.)

    International Nuclear Information System (INIS)

    Dickinson, J.R.

    1985-01-01

    Following the detection of reasonable levels of biologically active cytokinin-like compounds in one-month-old tomato plants, the possible involvement of {8- 14 C}-adenine and {1- 14 C}-isopentenyl pyrophosphate in the biosynthetic pathway leading to an accumulation of free zeatin derivatives, was studied. Intact tomato plants were used for a time-course study involving the uptake of {8- 14 C}-adenine and the tentative identification of compounds into which the 14 C became incorporated. Using high performance liquid chromatography, radioactive trans-zeatin was identified as being present in the Dowex 50 root extract. The 12-hour time interval was used and the roots of the tomato plants were immersed in a more heavily radiolabelled medium. Modified separation techniques were used to achieve enhanced radioactivity recovery rates. This experiment demonstrated the presence of relatively high levels of tentatively identified radioactive zeatin in the Dowex 50 root and stem extracts. Radioactivity in the aqueous extracts was found not to be contributed by cytokinin nucleotides. A final experiment was carried out using decapitated root systems to determine if the root tissue alone could be implicated in the synthesis of cytokinins. Decapitated tomato root systems were supplied with either {8- 14 C}-adenine or {1- 14 C}-isopentenyl pyrophosphate. The ratio of incorporation of {1- 14 C}-isopentenyl pyrophosphate into identified cytokinins was higher than for {8- 14 C}-adenine. It was concluded that both adenine and isopentenyl pyrophosphate are involved in the biosynthetic pathway leading to an accumulation of free zeatin derivatives in tomato roots

  2. Autoradiographic disposition of [1-methyl-14C]- and [2-14C]caffeine in mice

    International Nuclear Information System (INIS)

    Lachance, M.P.; Marlowe, C.; Waddell, W.J.

    1983-01-01

    Male, C57B1/6J mice received either [1-methyl-14C]caffeine or [2-14C]caffeine via the tail vein at a dose of 0.7 or 11 mg/kg, respectively. At 0.1, 0.33, 1, 3, 9, and 24 hr after treatment, the mice were anesthetized with ether and frozen by immersion in dry ice/hexane. The mice were processed for whole-body autoradiography by the Ullberg technique; this procedure does not allow thawing or contact with solvents. All autoradiographs revealed some retention of radioactivity at early time intervals in the lacrimal glands, seminal vesicle fluid, nasal and olfactory epithelium, and retinal melanocytes. The remaining portion of the animal was densitometrically uniform except for the lower levels noted in the CNS and adipose tissues. Excretion of radioactivity by the liver and kidneys seems to be the major routes of elimination. Localization in the liver at late time intervals was confined principally to the centrilobular region. Late sites of retention, observed only after [1-methyl-14C]caffeine administration, included the pancreas, minor and major salivary glands, splenic red pulp, thymal cortex, bone marrow, and gastrointestinal epithelium. Sites of localization present in both studies included the olfactory epithelium, lacrimal glands, hair follicles, and retinal melanocytes. Further studies are needed to determine whether the localization at these various sites is due to metabolic degradation, active transport, or possibly a specific receptor interaction

  3. Magnitude of 14C/12C variations based on archaeological samples

    International Nuclear Information System (INIS)

    Kusumgar, S.; Agrawal, D.P.

    1977-01-01

    The magnitude of 14 C/ 12 C variations in the period A.D. 5O0 to 200 B.C. and 370 B.C. to 2900 B.C. is discussed. The 14 C dates of well-dated archaeological samples from India and Egypt do not show any significant divergence from the historical ages. On the other hand, the corrections based on dendrochronological samples show marked deviations for the same time period. A plea is, therefore, made to study old tree samples from Anatolia and Irish bogs and archaeological samples from west Asia to arrive at a more realistic calibration curve. (author)

  4. Preparation and HPLC isolation of L-[U-14C]tryptophan from enzyme hydrolysate labelled with 14C

    International Nuclear Information System (INIS)

    Novak, J.; Tintera, S.; Hromadkova, B.

    1990-01-01

    Tryptophan was obtained from biomass of the blue-green alga Synechococcus elongatus cultivated under 14 CO 2 . After partial purification, the protein fraction was subjected to enzymatic hydrolysis using pronase. Semipreparative isolation of L-[U- 14 C]tryptophan was accomplished on a HPLC column of Separon S Hema 1000 CM, 2% ethanol were added to the eluent, and a precolumn packed with the basic anion exchanger Spheron 1000 DEAE was used. Always after the passage of L-[U- 14 C]tryptophan, the precolumn was decoupled. The substance was collected in 96% ethanol. After removing the solvent by vacuum evaporation, the sample was analyzed on a column packed with Separon SIX C 18 in the eluent of 0.1M-NaH 2 PO 4 , 2% methanol. When the desired radiochemical purity was not attained, the sample was purified on Separon SIX C 18 using 2% methanol. The final radiochemical purity achieved by using this method is 98%. (P.A.). 5 figs., 2 tabs., 4 refs

  5. Synthesis, Characterization and Thermal Decomposition Studies of Cr(III, Mn(II and Fe(III Complexes of N, N '-Bis[1,3-benzodioxol-5-ylmethylene]butane-1,4-diamine

    Directory of Open Access Journals (Sweden)

    Prasad M. Alex

    2009-01-01

    Full Text Available A bidentate Schiff base ligand namely, N,N'-bis-1,3-benzodioxol-5-ylmethylene]butane-1,4-diamine was synthesised by condensing piperonal (3,4-dioxymethylenebenzaldehyde with butane-1,4-diamine. Cr(III, Mn(II, Fe(III complexes of this chelating ligand were synthesised using acetates, chlorides, bromides, nitrates and perchlorates of these metals. The ligand and the complexes were characterised by elemental analysis, 1H NMR, UV-Vis and IR spectra, conductance and magnetic susceptibility measurements and thermogravimetric analysis. The thermograms of three complexes were analysed and the kinetic parameters for the different stages of decompositions were determined.

  6. The bomb 14C transient in the Pacific Ocean

    Science.gov (United States)

    Rodgers, Keith B.; Schrag, Daniel P.; Cane, Mark A.; Naik, Naomi H.

    2000-04-01

    A modeling study of the bomb 14C transient is presented for the Pacific Ocean. A primitive equation ocean circulation model has been configured for a high-resolution domain that accounts for the Indonesian Throughflow (ITF). Four separate runs were performed: (1) seasonal forcing with 20 Sv of ITF transport, (2) seasonal forcing with 10 Sv of ITF transport, (3) seasonal forcing with no ITF transport, and (4) interannual forcing with 15 Sv of ITF transport. This study has two main objectives. First, it is intended to describe the time evolution of the bomb 14C transient. This serves as a tool with which one can identify the physical processes controlling the evolving bomb 14C distribution in the Pacific thermocline and thus provides an interpretive framework for the database of Δ14C measurements in the Pacific. Second, transient tracers are applied to the physical oceanographic problem of intergyre exchange. This is of importance in furthering our understanding of the potential role of the upper Pacific Ocean in climate variability. We use bomb 14C as a dye tracer of intergyre exchange between the subtropical gyres and the equatorial upwelling regions of the equatorial Pacific. Observations show that while the atmospheric Δ14C signal peaked in the early to mid-1960s, the Δ14C levels in the surface water waters of the subtropical gyres peaked near 1970, and the Δ14C of surface waters in the equatorial Pacific continued to rise through the 1980s. It is shown that the model exhibits skill in representing the large-scale observed features observed for the bomb 14C transient in the Pacific Ocean. The model successfully captures the basin-scale inventories of bomb 14C in the tropics as well as in the extratropics of the North Pacific. For the equatorial Pacific this is attributed to the model's high meridional resolution. The discrepancies in the three-dimensional distribution of bomb 14C between the model and data are discussed within the context of the dynamical

  7. Bioconcentration of 14 C-Carbofuran and 14 C- Lindane in fresh water Tilapia Nilitica and the bioavailability of their residues to rats

    International Nuclear Information System (INIS)

    Aly, M.A.S.; Afifi, L.M.

    1997-01-01

    Tilapia Nilotica were exposed to 14 C- carbofuran (125 MUg/1) and 14 C - lindane (80 MUg/1) for 96 h. Uptake period followed by 8 days depuration period. The bioconcentration factor (BCF) for carbofuran reached 32.4 at 12 h and 82 for lindane at 48 h. The amount of 14 C-activity found in fish treated with 14 C - carbofuran after the uptake period showed the following descending order: viscera > remaining parts > gills > muscles. In case of 14 C - lindane treated fish the recovered amount followed the order; remaining parts> viscera > gills muscles. During the depuration period, carbofuran residues taken up by fish were eliminated in 2 phases, an initial rapid phase followed by a slower gradual one. However, the rate of elimination in case of lindane was much slower especially during the first 2 days. At the end of the depuration period (8 days), the muscles (edible portion) contained 10% and 58% of 14 C -activity in case of carbofuran and lindane treated groups, respectively. Both insecticides proved to be bioavailable when rats were fed treated fish. Of the administered dose, 44.1% and 53.0% were excreted in urine and feces case of 14 C-carbofuran while in case of 14 C - lindane it was 30.9% and 41.7% for urine and feces, respectively. 2 figs., 2 tabs

  8. Biodegradation mechanism of linear alkylbenzenesulfonate-14C

    International Nuclear Information System (INIS)

    Kubodera, Tadayoshi; Muto, Toshio; Yamamoto, Tatsuo

    1978-01-01

    The biodegradation of linear alkylbenzenesulfonate- 14 C (LAS- 14 C) tagged with 14 C at the linear side chain was studied on activated sludge by tracer method in addition to the methylene blue method which is widely employed in the biodegradation of LAS. It was found that there were three periods of rapid adsorption period, acclimation period, and degradation process. The radiolysis of dodecylbenzenesulfonate was studied on irradiating by 5000 Ci 60 Co source. The decomposition products were identified by GLC and GC-MS spectrometry after desulfonation. 1-Tetralone, 1-indanone, 4-methyl-1-tetralone, naphthalene et al. were found in them. (author)

  9. Synthesis of {sup 14}C-labeled levamisole and {sup 13}C-labeled tetramisole

    Energy Technology Data Exchange (ETDEWEB)

    Feil, V.J. [US Department of Agriculture, Agricultural Research Service, Biosciences Research Lab., Fargo, ND (United States)

    1996-12-01

    The syntheses of {sup 14}C-ring labeled levamisole ([-]-2,3,5,6-tetrahydro-6-phenyl [{sup 14}C]-UL imidazo[2,1-b]thiazole) from acetophenone-ring-UL-{sup 14}C in 5 steps plus resolution with a 7.5% overall yield, and {sup 13}C{sub 6}-ring labeled tetramisole ([{+-}]-2,3,5,6-tetrahydro-6-phenyl [{sup 13}C{sub 6}]imidazo[2,1-b]thiazole) from benzene-{sup 13}C{sub 6} in 6 steps with a 9.0% overall yield are described. (author).

  10. Synthesis of [14C]-labelled AY-30,068

    International Nuclear Information System (INIS)

    Hicks, D.R.; Hangeland, J.J.; Mobilio, D.; DeLange, B.

    1988-01-01

    [ 14 C]AY-30,068 (cis-1,8-diethyl-2,3,4,9-tetrahydro-4-(2-propenyl)-1H-carbazole-1-acetic acid), a potent analgesic agent, was prepared by incorporating [ 14 C]methyl iodide via a Wittig reaction. The intermediate aldehyde was synthesized in six steps from cis-1-ethyl-2-oxo-4-(2-propenyl)cyclohexaneacetic acid methyl ester. Three batches of the [ 14 C]labelled AY-30,068 were produced, giving a combined overall yield of 9% from [ 14 C]methyl iodide sp. act. 51.2, 17.7 and 4.4 μCi/mg; 97.5, 98.3, and 98.6% radiochemical purity, respectively. (author)

  11. Cerium dioxide (CeO2) nanoparticles decrease arsenite (As(III)) cytotoxicity to 16HBE14o- human bronchial epithelial cells.

    Science.gov (United States)

    Zeng, Chao; Nguyen, Chi; Boitano, Scott; Field, Jim A; Shadman, Farhang; Sierra-Alvarez, Reyes

    2018-07-01

    The production and application of engineered nanoparticles (NPs) are increasing in demand with the rapid development of nanotechnology. However, there are concerns that some of these novel materials could lead to emerging environmental and health problems. Some NPs are able to facilitate the transport of contaminants into cells/organisms via a "Trojan Horse" effect which enhances the toxicity of the adsorbed materials. In this work, we evaluated the toxicity of arsenite (As(III)) adsorbed onto cerium dioxide (CeO 2 ) NPs to human bronchial epithelial cells (16HBE14o-) using the xCELLigence real time cell analyzing system (RTCA). Application of 0.5 mg/L As(III) resulted in 81.3% reduction of cell index (CI, an RTCA measure of cell toxicity) over 48 h when compared to control cells exposed to medium lacking As(III). However, when the cells were exposed to 0.5 mg/L As(III) in the presence of CeO 2 NPs (250 mg/L), the CI was only reduced by 12.9% compared to the control. The CeO 2 NPs had a high capacity for As(III) adsorption (20.2 mg/g CeO 2 ) in the bioassay medium, effectively reducing dissolved As(III) in the aqueous solution and resulting in reduced toxicity. Transmission electron microscopy was used to study the transport of CeO 2 NPs into 16HBE14o- cells. NP uptake via engulfment was observed and the internalized NPs accumulated in vesicles. The results demonstrate that dissolved As(III) in the aqueous solution was the decisive factor controlling As(III) toxicity of 16HBE14o- cells, and that CeO 2 NPs effectively reduced available As(III) through adsorption. These data emphasize the evaluation of mixtures when assaying toxicity. Copyright © 2018 Elsevier Inc. All rights reserved.

  12. Measurement of C-14 distribution in forest around nuclear facilities

    International Nuclear Information System (INIS)

    Atarashi-Andoh, Mariko; Amano, Hikaru; Arakhatoon, Jahan

    2003-01-01

    A simple analytical method of C-14 measurement using fast bomb combustion and liquid scintillation counting (LSC) has been developed for measuring C-14 distribution in the terrestrial environment. Specific activities of C-14 in cedar leaves and soils collected from an area around nuclear facilities and control areas were measured using this method. Depth distribution of Cs-137 in soils was also measured at the same sampling sites and compared with the depth distribution of C-14. C-14 specific activity in cedar leaves examined around nuclear facilities exceeded that in the control areas by 8 to 30 mBq (g carbon) -1 . The depth distribution of C-14 in forest soil shows that C-14 has peak values in the top 10 cm of the soil profiles ascribed to the highest bomb C-14 level in the 1960's. The data were made available to assess the behavior of fallout C-14 in the surface environment. (author)

  13. Analysis of Δ14C variations in atmosphere

    International Nuclear Information System (INIS)

    Simon, J.; Sivo, A.; Richtarikova, M.; Holy, K.; Polaskova, A.; Bulko, M.; Hola, O.

    2005-01-01

    The Δ 14 C in the atmosphere have been measured and studied in two localities of Slovakia. The accomplished analysis proved the existence of the annual variations of the Δ 14 C with the attenuating amplitude and decreasing mean value. It seems to be logical and physically correct to describe the Δ 14 C time-dependence by the equation: y = Ae -at + Be -bt cos(ω 1 t + (φ)). The coefficients A, a, B, b, (φ) are listed in the table for both the localities. The observed variations of the Δ 14 C have a maximum in summer and minimum in winter .Probably it is caused by the higher requirement of the heat supply in winter season which is connected directly with the fossil CO 2 emissions and more intensive Suess effect. Summer maximum could be explained by the combination of the lower CO 2 emission rate and higher turbulent transport of the stratospheric 14 C to the troposphere. Using the Fourier harmonic analysis the amplitude spectra of the average annual variations were plotted. The obtained result shows that the variations have the high degree of symmetry. Furthermore, the obtained basic frequency ω 1 = 2π/12 [month -1 ] proves that the cyclic processes with the period of T = 12 [month] have a major influence on the 14 C amount in the troposphere. The presence of some higher-order harmonics is significant, but a physical interpretation has not yet been clear. In addition to the main frequency there are presented also 2ω 1 and 3ω 1 in Bratislava and 4ω 1 in Zlkovce data-set. The long-time average of the Δ 14 C in Zlkovce during years 1995-2004 is higher of about 6.6 o / oo than in Bratislava. It represents an unique evidence that the local CO 2 pollution affects the 14 C activity . The correlation on the level R 2 = 0,43 was found between Bratislava and Zlkovce atmospheric Δ 14 C data. (authors)

  14. C14 Assays and Autoradiographic Studies on the Rooster Comb

    Science.gov (United States)

    Balazs, Endre A.; Szirmai, John A.; Bergendahl, Gudrun

    1959-01-01

    The distribution of C14 was studied in various parts of the rooster comb following treatment with testosterone. The value of gas-phase assay of C14 in tissue has been demonstrated and the results compared with those of autoradiographic studies on the same tissue. The results of these experiments showed that androgen treatment significantly increases the rate of incorporation of C14 in various parts of the comb. The specific activity of carbon in the comb, cornea, and liver differed, depending on which precursor, viz. glucose-6-C14, glucose-1-C14, and glucuronolactone-U-C14, was administered. The highest values were obtained after the administration of glucose-6-C14; glucuronolactone-U-C14 gave the lowest specific activity. The specific activity of carbon in different parts of the comb showed considerable variation. Carbon assay of serial sections of the comb cut at various planes showed that the specific activity of carbon was highest in the mucoid layer. Both C14 assays and autoradiograms indicate that C14 is also present in other parts of the comb. As seen in autoradiography, the concentration of C14 was highest in the epithelium, in the blood vessel walls, and in the avascular collagenous tissue. These results, and indications from previous studies, suggest that the high specific activity of carbon in the mucoid layer is due mainly to the presence of C14-labelled hyaluronic acid. Autoradiograms and PAS staining suggest that a significant amount of C14 is also incorporated into the glycoproteins associated with the collagen fibers. PMID:13654453

  15. Organic compounds preparation with 14 C

    International Nuclear Information System (INIS)

    Shirvani, Gholam Hossein.

    1996-09-01

    Active urea is a basic reagent for the synthesis of active uric-8- 14 C acid. In our manner, activated Barium carbonate with specified activity was placed in a special furnace with ability of passing gases. Then, ammonia gas was passed through it at about 850 Degree C to obtain Barium Cyanamide. Reaction of the produced compound with CO 2 , and then acidification of the mixture, gave activated urea. Condensation of the urea with Ethylcyanoacetate, produce 6-Aminouracil which upon nitrosation, reduction and then condensation with urea, the desired Uric-8- 14 C acid was synthesized. (author). 148 refs.,

  16. Mechanical design of the third FnIII domain of tenascin-C.

    Science.gov (United States)

    Peng, Qing; Zhuang, Shulin; Wang, Meijia; Cao, Yi; Khor, Yuanai; Li, Hongbin

    2009-03-13

    By combining single-molecule atomic force microscopy (AFM), proline mutagenesis and steered molecular dynamics (SMD) simulations, we investigated the mechanical unfolding dynamics and mechanical design of the third fibronectin type III domain of tenascin-C (TNfn3) in detail. We found that the mechanical stability of TNfn3 is similar to that of other constituting FnIII domains of tenascin-C, and the unfolding process of TNfn3 is an apparent two-state process. By employing proline mutagenesis to block the formation of backbone hydrogen bonds and introduce structural disruption in beta sheet, we revealed that in addition to the important roles played by hydrophobic core packing, backbone hydrogen bonds in beta hairpins are also responsible for the overall mechanical stability of TNfn3. Furthermore, proline mutagenesis revealed that the mechanical design of TNfn3 is robust and the mechanical stability of TNfn3 is very resistant to structural disruptions caused by proline substitutions in beta sheets. Proline mutant F88P is one exception, as the proline mutation at position 88 reduced the mechanical stability of TNfn3 significantly and led to unfolding forces of < 20 pN. This result suggests that Phe88 is a weak point of the mechanical resistance for TNfn3. We used SMD simulations to understand the molecular details underlying the mechanical unfolding of TNfn3. The comparison between the AFM results and SMD simulations revealed similarities and discrepancies between the two. We compared the mechanical unfolding and design of TNfn3 and its structural homologue, the tenth FnIII domain from fibronectin. These results revealed the complexity underlying the mechanical design of FnIII domains and will serve as a starting point for systematically analyzing the mechanical architecture of other FnIII domains in tenascins-C, and will help to gain a better understanding of some of the complex features observed for the stretching of native tenascin-C.

  17. Review of C-14 inventory for the SFR facility

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Graham; Merino, Joan; Kerrigan, Emma

    2002-08-01

    The Swedish Radiation Protection Authority (SSI) is currently reviewing SKB's continuing assessment for disposal of radioactive waste to the SFR facility at Forsmark. Among the wastes disposed are reactor operating wastes. Among the relevant radionuclides is C-14, which is relatively difficult to measure and to control because of its mobility. This report documents a review of the C-14 inventory material submitted by SKB for the SFR-facility, to determine its validity and comment on the appropriate assumptions for C-14 content of wastes due to be disposed of to the SFR. The review is based on information provided by SSI as well as other relevant international experience. Conclusions are drawn upon: the chemical form of the C-14 in the waste from BWRs and PWRs; the production rate of C-14 in BWRs and PWRs and quantification of the source term in the IEX waste; the distribution of the C-14 in the IEX waste from BWR between the resins used for treatment of the primary cooling water and the resins used for treatment of the condensate water; quantification of the uncertainties. A suggestion is made that the C-14 inventory could be better developed based upon a mass balance assessment of all the C-14 produced in reactors, and its ultimate fate in effluent and solid wastes, taking account of the reactor specific operational factors identified in the review as relevant to C-14 inventory assessment.

  18. Review of C-14 inventory for the SFR facility

    International Nuclear Information System (INIS)

    Smith, Graham; Merino, Joan; Kerrigan, Emma

    2002-08-01

    The Swedish Radiation Protection Authority (SSI) is currently reviewing SKB's continuing assessment for disposal of radioactive waste to the SFR facility at Forsmark. Among the wastes disposed are reactor operating wastes. Among the relevant radionuclides is C-14, which is relatively difficult to measure and to control because of its mobility. This report documents a review of the C-14 inventory material submitted by SKB for the SFR-facility, to determine its validity and comment on the appropriate assumptions for C-14 content of wastes due to be disposed of to the SFR. The review is based on information provided by SSI as well as other relevant international experience. Conclusions are drawn upon: the chemical form of the C-14 in the waste from BWRs and PWRs; the production rate of C-14 in BWRs and PWRs and quantification of the source term in the IEX waste; the distribution of the C-14 in the IEX waste from BWR between the resins used for treatment of the primary cooling water and the resins used for treatment of the condensate water; quantification of the uncertainties. A suggestion is made that the C-14 inventory could be better developed based upon a mass balance assessment of all the C-14 produced in reactors, and its ultimate fate in effluent and solid wastes, taking account of the reactor specific operational factors identified in the review as relevant to C-14 inventory assessment

  19. 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

  20. Metabolism of apolipoproteins C-II, C-III, and B in hypertriglyceridemic men. Changes after heparin-induced lipolysis

    International Nuclear Information System (INIS)

    Huff, M.W.; Breckenridge, W.C.; Strong, W.L.; Wolfe, B.M.

    1988-01-01

    The C apolipoproteins are normally transferred to high density lipoproteins (HDL) after lipolysis of very low density lipoprotein (VLDL) triglyceride. In previous studies, a loss of plasma C apolipoproteins was documented after heparin-induced lipolysis in hypertriglyceridemic subjects. The present studies were designed to determine if this decline in plasma C apolipoproteins was due to their clearance with VLDL remnants. Five Type IV hypertriglyceridemic and two normal subjects were injected with 125I-VLDL and 131I-low density lipoproteins (LDL) to document kinetically an excess of VLDL apolipoprotein (apo) B flux relative to LDL apo B flux in the Type IV subjects. A mean of 46% VLDL apo B was cleared from the circulation, without conversion to intermediate density lipoprotein (IDL) or LDL. Heparin was then infused (9000 IU over 4 hours) to generate an excess of VLDL remnants that were not converted to IDL or LDL. VLDL triglyceride, apo B, and apo C concentrations fell at a similar rate. VLDL apo B declined by 42% (p less than 0.01). However, no increases were observed in IDL or LDL apo B in the Type IV subjects. This resulted in a 14% (p less than 0.01) decline in plasma apo B concentrations, indicating a clearance of VLDL remnants. VLDL apo C-II and C-III concentrations fell by 42% (p less than 0.025) and 52% (p less than 0.01), respectively. During the first 2.5 hours of infusion, they were almost quantitatively recovered in HDL. Thereafter, the C apolipoproteins declined in HDL during which time VLDL apo C concentrations continued to decline

  1. The HCM-linked W792R mutation in cardiac myosin-binding protein C reduces C6 FnIII domain stability.

    Science.gov (United States)

    Smelter, Dan F; de Lange, Willem J; Cai, Wenxuan; Ge, Ying; Ralphe, J Carter

    2018-06-01

    Cardiac myosin-binding protein C (cMyBP-C) is a functional sarcomeric protein that regulates contractility in response to contractile demand, and many mutations in cMyBP-C lead to hypertrophic cardiomyopathy (HCM). To gain insight into the effects of disease-causing cMyBP-C missense mutations on contractile function, we expressed the pathogenic W792R mutation (substitution of a highly conserved tryptophan residue by an arginine residue at position 792) in mouse cardiomyocytes lacking endogenous cMyBP-C and studied the functional effects using three-dimensional engineered cardiac tissue constructs (mECTs). Based on complete conservation of tryptophan at this location in fibronectin type II (FnIII) domains, we hypothesized that the W792R mutation affects folding of the C6 FnIII domain, destabilizing the mutant protein. Adenoviral transduction of wild-type (WT) and W792R cDNA achieved equivalent mRNA transcript abundance, but not equivalent protein levels, with W792R compared with WT controls. mECTs expressing W792R demonstrated abnormal contractile kinetics compared with WT mECTs that were nearly identical to cMyBP-C-deficient mECTs. We studied whether common pathways of protein degradation were responsible for the rapid degradation of W792R cMyBP-C. Inhibition of both ubiquitin-proteasome and lysosomal degradation pathways failed to increase full-length mutant protein abundance to WT equivalence, suggesting rapid cytosolic degradation. Bacterial expression of WT and W792R protein fragments demonstrated decreased mutant stability with altered thermal denaturation and increased susceptibility to trypsin digestion. These data suggest that the W792R mutation destabilizes the C6 FnIII domain of cMyBP-C, resulting in decreased full-length protein expression. This study highlights the vulnerability of FnIII-like domains to mutations that alter domain stability and further indicates that missense mutations in cMyBP-C can cause disease through a mechanism of

  2. Negative emotionality across diagnostic models: RDoC, DSM-5 Section III, and FFM.

    Science.gov (United States)

    Gore, Whitney L; Widiger, Thomas A

    2018-03-01

    The research domain criteria (RDoC) were established in an effort to explore underlying dimensions that cut across many existing disorders and to provide an alternative to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5). One purpose of the present study was to suggest a potential alignment of RDoC negative valence with 2 other dimensional models of negative emotionality: five-factor model (FFM) neuroticism and the DSM-5 Section III negative affectivity. A second purpose of the study, though, was to compare their coverage of negative emotionality, more specifically with respect to affective instability. Participants were adult community residents (N = 90) currently in mental health treatment. Participants received self-report measures of RDoC negative valence, FFM neuroticism, and DSM-5 Section III negative affectivity, along with measures of affective instability, borderline personality disorder, and impairment. Findings suggested that RDoC negative valence is commensurate with FFM neuroticism and DSM-5 Section III negative affectivity, and it would be beneficial if it was expanded to include affective instability. (PsycINFO Database Record (c) 2018 APA, all rights reserved).

  3. Modification by oral contraceptives in rat of 14C acetate incorporation into platelet lipids

    International Nuclear Information System (INIS)

    Ciavatti, M.; Renaud, S.

    1979-01-01

    The in vitro incorporation of acetate 14 C in platelet lipids was compared in control female rats (Gr.I) to rats treated for 4 days either by an oral contraceptive ethinyl oestradiol + lynestrenol (Gr.II), or by ethinyl oestradiol alone (Gr.III) or lynestrenol alone (Gr.IV). An increase of 43-45% in the incorporation of acetate could be ovserved in the two groups (II and III) which received ethinyl oestradiol, while the incorporation in group IV was similar to that of the controls. The lipid fractions of which the synthesis was the most considerably stimulated by the oestrogen treatment, were the neutral lipids as separated from the other lipids by TLC. In groups II and III the incorporation in cholesterol and cholesterol esters was increased by 8 fold and by 10 fold in the free fatty acid fraction. In these two groups, even in the phospholipid fractions PS + PI and PE, the radioactivity was significantly increased. The observed effect of the oral contraceptive studied here on platelet lipid synthesis in female rats, appears to be essentially due to the estrogens, since lynestrenol had only minimal effects in that respect. (orig.) [de

  4. 14C analysis via intracavity optogalvanic spectroscopy

    International Nuclear Information System (INIS)

    Murnick, Daniel; Dogru, Ozgur; Ilkmen, Erhan

    2010-01-01

    A new ultra sensitive laser-based analytical technique, intracavity optogalvanic spectroscopy (ICOGS), allowing extremely high sensitivity for detection of 14 C-labeled carbon dioxide has recently been demonstrated. Capable of replacing accelerator mass spectrometers (AMS) for many applications, the technique quantifies zeptomoles of 14 C in sub micromole CO 2 samples. Based on the specificity of narrow laser resonances coupled with the sensitivity provided by standing waves in an optical cavity, and detection via impedance variations, limits of detection near 10 -1514 C/ 12 C ratios have been obtained with theoretical limits much lower. Using a 15 W 14 CO 2 laser, a linear calibration with samples from 5 x 10 -15 to >1.5 x 10 -12 in 14 C/ 12 C ratios, as determined by AMS, was demonstrated. Calibration becomes non-linear over larger concentration ranges due to interactions between CO 2 and buffer gas, laser saturation effects and changes in equilibration time constants. The instrument is small (table top), low maintenance and can be coupled to GC or LC input. The method can also be applied to detection of other trace entities. Possible applications include microdosing studies in drug development, individualized sub-therapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon.

  5. 15C-15F Charge Symmetry and the 14C(n,γ)15C Reaction Puzzle

    International Nuclear Information System (INIS)

    Timofeyuk, N.K.; Thompson, I.J.; Baye, D.; Descouvemont, P.; Kamouni, R.

    2006-01-01

    The low-energy reaction 14 C(n,γ) 15 C provides a rare opportunity to test indirect methods for the determination of neutron capture cross sections by radioactive isotopes versus direct measurements. It is also important for various astrophysical scenarios. Currently, puzzling disagreements exist between the 14 C(n,γ) 15 C cross sections measured directly, determined indirectly, and calculated theoretically. To solve this puzzle, we offer a strong test based on a novel idea that the amplitudes for the virtual 15 C→ 14 C+n and the real 15 F→ 14 O+p decays are related. Our study of this relation, performed in a microscopic model, shows that existing direct and some indirect measurements strongly contradict charge symmetry in the 15 C and 15 F mirror pair. This brings into question the experimental determinations of the astrophysically important (n,γ) cross sections for short-lived radioactive targets

  6. Behavior of 14C-BHC residues in rice grain

    International Nuclear Information System (INIS)

    Lee, S.R.; Kim, Y.H.

    1981-01-01

    γ-(U- 14 C)-BHC was applied to rice plants grown in a pot and its fate in the growth, polishing and oil-extraction processes of the grain was investigated. The 14 C-activity was absorbed and translocated widely in the plant and the recovery of applied 14 C-activity in the straw and grain was about 2.8%, of which 9.4% was found in the brown rice. The % partitioning of 14 C-residues in bran and polished rice was 12:88 and that in oil and oilcake was 37:63. Characterization of 14 C-residues the presence of γ-BHC, pentachlorocyclohexene, trichlorobenzene and hydrophilic metabolites, whose proportions were different in the straw and grain. (Author)

  7. Appearance of circulating and tissue 14C-lipids after oral 14C-tripalmitate administration in the late pregnant rat

    International Nuclear Information System (INIS)

    Argiles, J.; Herrera, E.

    1989-01-01

    Studies were performed to determine whether and/or how dietary lipids participate in maternal hypertriglyceridemia during late gestation in the rat. After oral administration of glycerol-tri(1-14C)-palmitate, total radioactivity in plasma increased more rapidly in 20-day pregnant rats than in either 19-day pregnant rats or virgin controls. At the peak of plasma radioactivity, four hours after the tracer was administered, most of the plasma label corresponded to 14C-lipids in triglyceride-rich lipoproteins (d less than 1.006), and when expressed per micromol of triglyceride, values were higher in pregnant than in virgin rats. The difference was less after 24 hours, although at this time the level of 14C-lipids in d less than 1.006 lipoproteins was still higher in 20-day pregnant rats than in virgins. Tissue 14C-lipids, as expressed per gram of fresh weight, were similar in pregnant and virgin rats, but the values in mammary glands were much higher in the former group. Estimated recovery of administered radioactivity four hours after tracer in total white adipose tissue, mammary glands, and plasma lipids was higher in pregnant than in virgin rats. No difference was found between 20-day pregnant and virgin rats either in the label retained in the gastrointestinal tract or in that exhaled as 14C-CO2 during the first four hours following oral administration of 14C-tripalmitate. These findings plus the known maternal hyperphagia, indicate that in the rat at late pregnancy triglyceride intestinal absorption is unchanged or even enhanced and that dietary lipids actively contribute to both maternal hypertriglyceridemia and lipid uptake by the mammary gland

  8. Accelerator mass spectrometry analysis of "1"4C-oxaliplatin concentrations in biological samples and "1"4C contents in biological samples and antineoplastic agents

    International Nuclear Information System (INIS)

    Toyoguchi, Teiko; Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi; Kato, Kazuhiro; Tokanai, Fuyuki

    2015-01-01

    Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the "1"4C concentration in "1"4C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) – AMS system. The calibration curves of "1"4C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a "1"4C content of water in three vacuum blood collection tubes and a syringe were measured. "1"4C was not detected from water in these devices. The mean "1"4C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of "1"4C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, "1"4C contents of the antineoplastic agents were quantitated. "1"4C contents were different among 10 antineoplastic agents; "1"4C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

  9. Accelerator mass spectrometry analysis of {sup 14}C-oxaliplatin concentrations in biological samples and {sup 14}C contents in biological samples and antineoplastic agents

    Energy Technology Data Exchange (ETDEWEB)

    Toyoguchi, Teiko, E-mail: tteiko@med.id.yamagata-u.ac.jp [Department of Pharmacy, Yamagata University Hospital, 2-2-2 Iida-Nishi, Yamagata-shi, Yamagata 990-9585 (Japan); Kobayashi, Takeshi; Konno, Noboru; Shiraishi, Tadashi [Department of Pharmacy, Yamagata University Hospital, 2-2-2 Iida-Nishi, Yamagata-shi, Yamagata 990-9585 (Japan); Kato, Kazuhiro; Tokanai, Fuyuki [Department of Physics, Faculty of Science, Yamagata University, 1-4-12 Kojirakawa-machi, Yamagata-shi, Yamagata 990-8560 (Japan)

    2015-10-15

    Accelerator mass spectrometry (AMS) is expected to play an important role in microdose trials. In this study, we measured the {sup 14}C concentration in {sup 14}C-oxaliplatin-spiked serum, urine and supernatant of fecal homogenate samples in our Yamagata University (YU) – AMS system. The calibration curves of {sup 14}C concentration in serum, urine and supernatant of fecal homogenate were linear (the correlation coefficients were ⩾0.9893), and the precision and accuracy was within the acceptance criteria. To examine a {sup 14}C content of water in three vacuum blood collection tubes and a syringe were measured. {sup 14}C was not detected from water in these devices. The mean {sup 14}C content in urine samples of 6 healthy Japanese volunteers was 0.144 dpm/mL, and the intra-day fluctuation of {sup 14}C content in urine from a volunteer was little. The antineoplastic agents are administered to the patients in combination. Then, {sup 14}C contents of the antineoplastic agents were quantitated. {sup 14}C contents were different among 10 antineoplastic agents; {sup 14}C contents of paclitaxel injection and docetaxel hydrate injection were higher than those of the other injections. These results indicate that our quantitation method using YU-AMS system is suited for microdosing studies and that measurement of baseline and co-administered drugs might be necessary for the studies in low concentrations.

  10. The synthesis of Org 3770 labelled with 3H, 13C and 14C

    International Nuclear Information System (INIS)

    Kaspersen, F.M.; Rooij, F.A.M. van; Sperling, E.G.M.; Wieringa, J.H.

    1989-01-01

    The syntheses of 1,2,3,4,10,14b-hexahydro-2-methylpyrazino[2,1-a]pyrido[2,3-c][2]benazepine (Org 3770) labelled with 3 H (and 2 H), 13 C and 14 C are described. Tritiated Org 3770 was prepared either by exchange under alkaline conditions with tritiated water or catalytic reductive dehalogenation of a chloro analogue with 3 H 2 . 13 C-labelled material was obtained in a seven-step synthesis starting from 13 C-labelled benzene whereas 14 C-Org 3770 was prepared in a three-step synthesis starting with 14 CO 2 . All labelled compounds were analyzed by TLC, HPLC, MS and NMR. (author)

  11. Evaluation of [14C] and [13C]Sucrose as Blood-Brain Barrier Permeability Markers.

    Science.gov (United States)

    Miah, Mohammad K; Chowdhury, Ekram A; Bickel, Ulrich; Mehvar, Reza

    2017-06-01

    Nonspecific quantitation of [ 14 C]sucrose in blood and brain has been routinely used as a quantitative measure of the in vivo blood-brain barrier (BBB) integrity. However, the reported apparent brain uptake clearance (K in ) of the marker varies widely (∼100-fold). We investigated the accuracy of the use of the marker in comparison with a stable isotope of sucrose ([ 13 C]sucrose) measured by a specific liquid chromatography-tandem mass spectrometry method. Rats received single doses of each marker, and the K in values were determined. Surprisingly, the K in value of [ 13 C]sucrose was 6- to 7-fold lower than that of [ 14 C]sucrose. Chromatographic fractionation after in vivo administration of [ 14 C]sucrose indicated that the majority of the brain content of radioactivity belonged to compounds other than the intact [ 14 C]sucrose. However, mechanistic studies failed to reveal any substantial metabolism of the marker. The octanol:water partition coefficient of [ 14 C]sucrose was >2-fold higher than that of [ 13 C]sucrose, indicating the presence of lipid-soluble impurities in the [ 14 C]sucrose solution. Our data indicate that [ 14 C]sucrose overestimates the true BBB permeability to sucrose. We suggest that specific quantitation of the stable isotope ( 13 C) of sucrose is a more accurate alternative to the current widespread use of the radioactive sucrose as a BBB marker. Copyright © 2017 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  12. 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

  13. Sources of C-14 generation and associated doses

    International Nuclear Information System (INIS)

    Amado, Valeria A.; Biaggio, Alfredo L.; Canoba, Analia C.; Curti, Adriana R.

    2009-01-01

    C-14 is a radioactive isotope of C with a half-life of 5700 years that decays to N-14 by emission of beta radiation. It is naturally produced in the upper atmosphere by cosmic ray neutrons via the (n;p) reaction over N-14. Anthropogenic C-14 has been generated in the past by atmospheric nuclear weapon tests and it is currently produced during the operation of nuclear reactors. Once released this radionuclide behaves in the biosphere as the standard carbon cycle. Since the beginning of the industrial period the relationship Carbon-14/Stable Carbon has changed continuously, and so the dose incurred by the world population. In this paper the main anthropogenic activities that modified such relationship are presented and analyzed: the Suess effect and the generation of nuclear energy. It is concluded that the current trend of reduction of the total dose due to C-14 will continue during the next decades. Finally it is indicated that in order to prevent an excessive accumulation of this radionuclide in the biosphere, actions should be collectively implemented to be effective. (author) [es

  14. Radiocarbon 14C differentiation of sparkling and carbonated wines

    International Nuclear Information System (INIS)

    Martin, G.E.; Krueger, H.W.; Burggraff, J.M.

    1985-01-01

    Specific 14 C-activities, percent of modern 14 C-activity, and calculated percent of fermentation CO 2 are presented for CO 2 contained in commercial sparkling wines, labeled as champagne or produced by the bulk (charmat) process. These data are given for the production years 1976-1982. The survey encompassed effervescent wines produced in Spain, Italy, West Germany, California, and New York. Addition of synthetic CO 2 to approximately 40 samples represented as sparkling wines was indicated by low 14 C-activities of CO 2 in these wines. Data for 14 C-activity were also presented for the ethanol distilled from sparkling wines for the years 1977-1980. In all cases, the 14 C-activity of ethanol was appropriate to the year of vintage

  15. Changes in the level of [14C]indole-3-acetic acid and [14C]indoleacetylaspartic acid during root formation in mung bean cuttings

    International Nuclear Information System (INIS)

    Norcini, J.G.; Heuser, C.W.

    1988-01-01

    Changes in the levels of [ 14 C]indole-3-acetic acid (IAA) and [ 14 C]indoleacetylaspartic acid (IAAsp) were examined during adventitious root formation in mung bean (Vigna radiata [L.] R. Wilcz. Berken) stem cuttings. IAAsp was identified by GC-MS as the primary conjugate in IAA-treated cuttings. During root formation in IAA-treated cuttings, the level of [ 14 C]IAAsp increased rapidly the first day and then declined; [ 14 C]IAA was rapidly metabolized and not detected after 12 hours

  16. Comparative in vitro metabolism of 1-14C-oleic acid and 1-14C-erucic acid in liver, heart and skeletal muscles of rats

    International Nuclear Information System (INIS)

    Bhatia, I.S.; Sharma, A.K.; Ahuja, S.P.

    1978-01-01

    In vitro oxidation of 14 C-oleic and 1- 14 C-erucic acid and their incorporation into lipids by liver, heart and skeletal muscles from female albino rats were studied. These tissues were obtained from rats maintained for 120 days on low fat diet or diets containing 15% mustard oil or 15% groundnut oil. In all these tissues from rats on different types of diets, the oxidation of 1- 14 C-erucic acid was lower than that 1- 14 C-oleic acid. There was little accumulation of lipids in heart after 120 days of feeding mustard oil. Oxidation of 1- 14 C-erucic acid was enhanced in liver, heart and skeletal muscles of rats conditioned to the mustard oil diet supplying erucic acid. Oxidation of erucic acid was maximum in liver and least in heart, whereas there were no differences in the oxidation of 1- 14 C-oleic acid in these tissues. Incorporation of 1- 14 C-oleic acid into triglycerides and phospholipids was not affected by the type of diet or tissues Incorporation of 1- 14 C-erucic acid was mainly into triglycerides of heart and skeletal muscles of rats not accustomed to mustard oil diet whereas these tissues from rats accustomed to mustard oil diets incorporated 1- 14 C-erucic acid both into the triglycerides and phospholipids. (author)

  17. Correction procedures for C-14 dates

    International Nuclear Information System (INIS)

    McKerrell, H.

    1975-01-01

    There are two quite separate criteria to satisfy before accepting as valid the corrections to C-14 dates which have been indicated for some years now by the bristlecone pine calibration. Firstly the correction figures have to be based upon all the available tree-ring data and derived in a manner that is mathematically sound, and secondly the correction figures have to produce accurate results on C-14 dates from archaeological test samples of known historical date, these covering as wide a period as possible. Neither of these basic prerequisites has yet been fully met. Thus the two-fold purpose of this paper is to bring together, and to compare with an independently based procedure, the various correction curves or tables that have been published up to Spring 1974, as well as to detail the correction results on reliable, historically dated Egyptian, Helladic and Minoan test samples from 3100 B.C. The nomenclature followed is strictly that adopted by the primary dating journal Radiocarbon, all C-14 dates quoted thus relate to the 5568 year half-life and the standard AD/BC system. (author)

  18. Application of AMS 14C measurements to criminal investigations

    International Nuclear Information System (INIS)

    Nakamura, T.; Ohta, T.; Nishida, M.; Ikeda, A.; Oda, H.; Kojima, S.; Niu, E.

    2005-01-01

    14 C variations of atmospheric CO 2 as well as carbonaceous materials of human body, such as collagen fractions from teeth and bone, tissue, hair, nail, etc., of modern humans dead or alive, are influenced by 14 C produced artificially by nuclear bomb tests in the atmosphere from late 1950s to early 1960s. By careful investigation of 14 C concentration of tree rings and human tissue samples formed in this time ranges, we can establish a relation between their 14 C concentrations and calendar year. By applying this relation to a sample whose 14 C concentration can be measured, we can estimate the formation age of the sample. In addition, sources of the drugs that were used in some criminal cases can be possibly identified by the analysis of their carbon isotope ratios ( 13 C/ 12 C and 14 C/ 12 C). This method of age determination was applied to a forensic study; i.e., to two similar cases of murder. One of the two cases is for a dead body of a modern human who was killed in 1978 and buried under the floor of the house owned by the murderer. The body was excavated in 2004 according to the confession by the murderer. 14 C abundances of several pieces of hair and one tooth (the third molar) from the body were measured with accelerator mass spectrometry (AMS), and compared with the annual change on concentrations of bomb-produced 14 C. The time of death of the body was estimated to be at around 1977, and her age was from 30 to 37 years old at that time. These estimations were consistent with the real values that were revealed after the case was solved by the confession of the real murderer who gave himself up to the police. For the other case, 14 C analysis was also consistent with the fact revealed by police investigations as well as by the confession of the real murderer.

  19. Dating human DNA with the 14C bomb peak

    Energy Technology Data Exchange (ETDEWEB)

    Kutschera, Walter; Liebl, Jakob; Steier, Peter [VERA Laboratory, University of Vienna, Vienna (Austria)

    2013-07-01

    In 1963 the limited nuclear test ban treaty stopped nuclear weapons testing in the atmosphere. By then the addition from bomb-produced {sup 14}C had doubled the {sup 14}C content of the atmosphere. Through the CO{sub 2} cycle this excess exchanged with the hydrosphere and biosphere leading to a rapidly decreasing {sup 14}C level in the atmosphere. Today we are almost back to the pre-nuclear level. As a consequence all people on Earth who lived during the second half of the 20th century were exposed to this rapidly changing {sup 14}C signal. A few years ago, a group at the Department of Cell and Molecular Biology of the Karolinska Institute in Stockholm started to use the {sup 14}C bomb peak signal in DNA to determine retrospectively the age of cells from various parts of the human body (brain, heart, fat). In a collaboration with this group, we have studied the age of olfactory bulb neurons in the human brain. For this investigation, {sup 14}C AMS measurements were developed at VERA for very small carbon samples in the range from 2 to 4 micrograms. In the presentation the general concept of {sup 14}C bomb peak dating of human DNA and several applications are discussed.

  20. 14C glucose uptake and turnover, a biomarker in benzo(a)pyrene induced lung carcinogenesis: role of curcumin and resveratrol

    International Nuclear Information System (INIS)

    Malhotra, Anshoo; Nair, P.; Dhawan, D.K.

    2010-01-01

    Full text: The aim of the present study was to explore the synergistic potential of curcumin and resveratrol in modulation of glucose metabolism by studying 14 C glucose uptake, turnover in the lung slices and ultra-histoarchitectural changes during benzo(a)pyrene (BP) induced lung carcinogenesis in mice. The mice were segregated into five treatment groups which included group I (normal control), group II (BP treated), group III (BP+curcumin treated), group IV (BP+resveratrol treated) and group V (BP+curcumin+resveratrol treated). Animals in Group II were given a single intraperitoneal injection of Benzo(a)pyrene in corn oil at a dose level of 100mg/Kg body weight. Group III animals were given curcumin orally in drinking water at a dose level of 60 mg /Kg/ body weight, thrice a week. Animals in Group IV were given resveratrol orally at a dose level of 5.7 microgram/ml drinking water, thrice a week. Animals in group V were given a combined treatment of curcumin and resveratrol in a similar manner as was given to group III and group IV animals, respectively. All the animals had free access to the diet and water and the treatments continued for a total duration of 22 weeks. The morphological and ultra-histoachitectural analyses confirmed lung carcinogenesis, in the BP treated mice. Tumor incidence and tumor multiplicity were observed to be 88% and 1.75 respectively in the BP treated mice. A statistically significant increase in the uptake of 14 C glucose was observed in the lung slices of BP treated mice. Further, radiorespirometric analyses of 14 C turnover also showed a significant increase in the lung slices of BP treated mice. The ultra-histoarchitecture of the BP treated mice revealed disruption in cellular integrity along with nuclear deformation. Mitochondria were swollen and cytoplasm appeared granular along with extensive vacuolization. Further, spaces between the endothelium, epithelium and basement membrane indicative of lung injury and edema were observed

  1. A critical review of atmospheric 14 C activities

    International Nuclear Information System (INIS)

    Krajcar Bronic, I.; Horvatincic, N.; Baresic, J.; Obelic, B.; Vreca, P.

    2006-01-01

    14 C activity of atmospheric CO 2 has been measured at the Rudjer Boskovi Institute as a part of environmental monitoring in order to determine possible differences between clean-air sites, industrialized city and sites in the vicinity of nuclear power plant. Samples of CO 2 from the atmosphere have been collected by absorption of CO 2 on the saturated carbonate-free NaOH solution for a period of 1 month under stationary conditions. The obtained Na 2 CO 3 has been dissolved in HCl and the produced CO 2 used for CH 4 preparation by catalytic reaction with H 2 at 450 degrees Celsius. A gas proportional counter filled with CH 4 has been used for 14 C activity measurement. The method of collection of CO 2 does not require any power source and can be therefore used for sampling at the remote sites, such as mountains or forests. However,due to the lack of mixing of the Na OH solution, the absorption process is limited on the surface of the solution, and there exists the possibility of fractionation of carbon isotopes due to different reaction rate constants of 12 C and 13 C. A continuous record of atmospheric 14 CO 2 activity exists for the city of Zagreb (1986 to 2005), while shorter records (1-2 years) exist for several other sites of various characteristics: two clean-air sites (Mt. Medvednica, altitude about 1000 m a.s.l., for period 1995 to 1996, and the Plitvice National Park for period 2003 to 2005), and a site close to the Nuclear Power Plant Krsko (1984 to 1986).Within the bilateral Croatian-Slovene project we have recently measured also the stable isotope composition (δ13 C) of Na 2 CO 3 collected at two different sampling sites in order to determine seasonal fluctuations in both 14 C and 13 C isotope composition. Unexpectedly low δ13 C values have been obtained about (-25±2)0/00 instead of expected (-7±1)0/00. Such low values have been attributed to the carbon isotope fractionation during the CO 2 absorption on the highly alkaline medium because of

  2. 14CO2-assimilation, translocation of 14C, and 14C-carbonate uptake in different organs of spring barley plants in relation to adult-plant resistance to powdery mildew

    International Nuclear Information System (INIS)

    Hwang, B.K.; Ibenthal, W.-D.; Heitefuss, R.

    1986-01-01

    The cultivar Peruvian of spring barley, which is susceptible at all growth stages, and Asse, which exhibits adult-plant resistance to powdery mildew, were compared in 14 CO 2 assimilation, distribution of 14 C, and 14 C-carbonate uptake in different organs of healthy and infected plants. The reduction of 14 CO 2 assimilation in infected plants at the first and fourth leaf stages was greater in Peruvian than in Asse. In Peruvian, the 14 C which was fixed by the infected third leaf of plants with mildew on the lower 3 leaves remained in the third leaves with very little translocation to other parts of the plant. Infection of the lower three leaves at the fourth leaf stage reduced 14 CO 2 assimilation in noninfected fourth leaves of Asse less than that of Peruvian, but the flow of 14 C from the healthy fourth leaves into other plant parts such as leaf sheaths was markedly stimulated in Peruvian compared to Asse. Infection also reduced the uptake of 14 C-carbonate by seedling roots, the reduction being greater in Peruvian than Asse. A greater proportion of the 14 C absorbed by roots of Asse was translocated to the infected leaves than that of Peruvian. It was concluded that powdery mildew disrupted the normal pattern of photosynthesis and translocation of metabolites in a susceptible cultivar more markedly than in an adult-plant-resistant cultivar of spring barley. (author)

  3. Processing ix spent resin waste for C-14 isotope recovery

    International Nuclear Information System (INIS)

    Chang, F. H.; Woodall, K. B.; Sood, S. K.; Vogt, H. K.; Krochmainek, L. S.

    1991-01-01

    A process developed at Ontario Hydro for recovering carbon-14 (C-14) from spent ion exchange resin wastes is described. Carbon-14 is an undesirable by-product of CANDU 1 nuclear reactor operation. It has an extremely long (5730 years) half-life and can cause dosage to inhabitants by contact, inhalation, or through the food cycle via photosynthesis. Release of carbon-14 to the environment must be minimized. Presently, all the C-14 produced in the Moderator and Primary Heat Transport (PHT) systems of the reactor is effectively removed by the respective ion exchange columns, and the spent ion exchange resins are stored in suitably engineered concrete structures. Because of the large volumes of spent resin waste generated each year this method of disposal by long term storage tends to be uneconomical; and may also be unsatisfactory considering the long half-life of the C-14. However, purified C-14 is a valuable commercial product for medical, pharmaceutical, agricultural, and organic chemistry research. Currently, commercial C-14 is made artificially in research reactors by irradiating aluminum nitride targets for 4.5 years. If the C-14 containing resin waste can be used to reduce this unnecessary production of C-14, the total global build-up of this radioactive chemical can be reduced. There is much incentive in removing the C-14 from the resin waste to reduce the volume of C-14 waste, and also in purifying the recovered C-14 to supply the commercial market. The process developed by Ontario Hydro consists of three main steps: C-14 removal from spent resins, enrichment of recovered C-14, and preparation of final product. Components of the process have been successfully tested at Ontario Hydro's Research Division, but the integration of the process is yet to be demonstrated. A pilot scale plant capable of processing 4 m 3 of spent resins annually is being planned for demonstrating the technology. The measured C-14 activity levels on the spent resins ranged from 47

  4. Synthesis of 1-benzyl-4-((5,6-dimethoxy(2- sup 14 C)-1-indanon)-2-YL)-methylpiperidine hydrochloride (E2020- sup 14 C)

    Energy Technology Data Exchange (ETDEWEB)

    Iimura, Youichi; Mishima, Mannen; Sugimoto, Hachiro (Eisai Co., Ltd., Ibaraki (Japan). Tsukuba Research Labs.)

    1989-07-01

    1-Benzyl-4-((5,6-dimethoxy(2-{sup 14}C)-1-indanon)-2-yl)-methylpiperidine hydrochloride (E2020-{sup 14}C), and acetylcholinesterase inhibitor for studying the pharmacokinetic profiles of E2020, was synthesized from 5,6-dimethoxy(2-{sup 14}C)-1-indanone as the labelled starting material. (author).

  5. Photosynthetic incorporation of 14C by Stevia rebaudiana

    International Nuclear Information System (INIS)

    Ferraresi, M. de L.; Ferraresi Filho, O.; Bracht, A.

    1985-01-01

    The photosynthetic incorporation of 14 by Stevia rebaudiana specimens was investigated. The 14 C incorporation, when the isotope was furnished to the plant in form of 14 CO 2 , was rapid. After 24 hours, the radioactivity has been incorporated into a great number of compounds including pigments, terpenes, glucose, cellulose and also stevioside and its derivatives. (M.A.C.) [pt

  6. Residues of 14C-cyolane in cottonseed products

    International Nuclear Information System (INIS)

    Zayed, S.M.A.D.; Osman, A.Z.; Fakhr, I.M.I.; Bahig, M.E.

    1981-01-01

    The systemic insecticide cyolane [2-(0,0-diethylphosphoryl)-imino-1,3-dithiolane] was prepared from 14 C-ethanol, phosphorus oxychloride and 2-amino-1,3-dithiolane. Cotton plants were treated with two applications of the insecticide under conditions of local agricultural practice. 14 C-residues in the crude oil and cake of the harvested cotton seeds amounted to 1.63 and 0.014 mg/kg respectively. About 50% of the 14 C-activity present in the crude oil was found to be eliminated by simulated commercial processes used for refining of the oil. Alkali treatment and bleaching removed 16% and 25% of the radioactive residues respectively. Winterization of the bleached oil at 5-7 0 C for 3 days effected a further elimination of 13%. 14 C-residues in the cotton seed products and in the samples of the refined oil were characterized and the main constituents identified using chromatographic techniques. (author)

  7. 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

  8. Environmental background 14C levels in Japan in 1990s

    International Nuclear Information System (INIS)

    Fuma, Shoichi; Inoue, Yoshikazu; Miyamoto, Kiriko; Takeda, Hiroshi; Iwakura, Tetsuo; Arai, Kiyohiko; Kashida, Yoshihiko; Ichimasa, Yusuke

    2002-01-01

    For assessment of radiation doses due to 14 C released from nuclear facilities, it is necessary to know the background level of environmental 14 C originated from the natural cosmic-ray production and the past atmospheric nuclear weapons tests. The authors selected grapes as an indicator of 14 C levels in the environment including atmosphere, and determined the specific activities of 14 C in ethanol extracted from wine made from grapes cultivated in several prefectures or unknown places in Japan in each year from 1990 to 2000. The specific activities of 14 C were almost uniform all over Japan in each year, though they showed the weak tendency to slightly decrease with increasing population densities in the prefecture where the wine grapes were cultivated. It is considered that this small regional variation in the specific activities of 14 C arose from Suess effect, because population densities can be regarded as an index of the amount of CO 2 emission from fossil-fuel combustion. The specific activities of 14 C gradually decreased in the 1990s. That is, they were 260 mBq/gC in 1990, and became 244 mBq/gC in 2000. This 14 C level in 2000 was still about 7% higher than the pre-bomb level. The decrease in 14 C originated from the past atmospheric nuclear weapons tests could be described by a single exponential function with a half-time of 10.3 years in 1990s. This half-time was shorter than that in the Europe, Canada and the South Pacific. This difference in the decreasing rate between Japan and other countries may be explained by a fact that the amount of CO 2 emission from fossil-fuel combustion continued to increase in Japan in this period. The specific activities of 14 C in wine ethanol determined in this study showed good agreement with those in atmospheric CO 2 predicted by a mathematical model. They were also in the same levels as the 14 C specific activities in atmospheric CO 2 , tree leaves, grass and plant food in Japan and other countries, which were

  9. Synthesis of phenobarbital {sup 14}C - 5 (1964); Synthese du phenobarbital {sup 14}C - 5 (1964)

    Energy Technology Data Exchange (ETDEWEB)

    Benakis, A [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    Phenobarbital (Luminal), well known as a hypnotic agent, plays also an important role in the medical treatment of epilepsy. With the object of studying the metabolism of this medicament in the living system, the synthesis of phenobarbital marked in position 2 of the pyrimidinic ring has been effected. It has been necessary, in order to carry out to research into the metabolism of this product, to have a phenobarbital marked in position 5 of the pyrimidinic ring. This synthesis, making it possible to introduce C-14 into position 5 of the pyrimidinic ring, consists of seven stages starting from C-14 carboxyl benzoic acid having a specific activity of 25 mc/mM. The melting point of the final product is 172 - 173 deg. C and its specific activity is 11.15 mc/mM. The overall radioactive yield of the pure product, with respect to the original benzoic acid (10 mM) is of the order of 3 per cent. The purity of the product has been controlled by paper chromatography; it is of the order of 99 per cent. (author) [French] Le phenobarbital (Luminal) bien connu comme agent hypnotique, joue egalement un role important dans la medication anti-epileptique. Pour l'etude du metabolisme de ce medicament dans l'organisme vivant, nous avons synthetise le phenobarbital marque en position 2 du cycle pyrimidinique. Afin de poursuivre la recherche du metabolisme de ce produit, il a ete necessaire de disposer du phenobarbital marque en position 5 du cycle. pyrimidinique. Cette synthese, permettant l'introduction du {sup 14}C en position 5 du cycle pyrimidinique, comporte sept etapes, au depart de l'acide benzoique carboxyle {sup 14}C, d'une activite specifique de 25 mc/mM. Point de fusion du produit final: 172 - 173 deg. C Activite specifique: 11,15 mC/mM. Rendement total radioactif du produit pur, par rapport a l'acide benzoique de depart sur 10 mM, de l'ordre de 3 pour cent. La purete du produit a ete controlee par chromatographie sur papier; elle est de l'ordre de 99 pour cent. (auteur)

  10. Distribution of 14C in soil and rice plants following application of 14C - parathion to soil

    International Nuclear Information System (INIS)

    Andrea, M.M. de; Ruegg, E.F.

    1983-01-01

    Amount of residues of 14 C-parathion in soil rice plants after application of the insecticide to soil were determined in four systems studied during five weeks: pots of soil with and without plants and open or enclosed by a transparent cover. Measurements of amounts volatilized and 14 CO 2 evolution from the pesticide were made in closed system without plants. The bound residues in soil and plants were also determined. Results indicated that parathion half life in a Gley Humic soil was about two weeks. Very little radiocarbon was taken up by rice plants; of this, more was found in shoots of plants enclosed, probably by collection of the volatilized material by plants. About 6% and 4% of the 14 C-parathion were found as volatilized material and 14 CO 2 , respectively after five weeks. Bound residues varied very little and reached a maximum of 22% in soil and in plants amounted to less than 2% at the final of the experiment. (Author) [pt

  11. Synthesis of 14C labelled lidocaine (α-diethylamino acet-2,6-dimethylanilide)

    International Nuclear Information System (INIS)

    Zhou Zhentang; Qian Guojun; Lin Fenzhi; Zhuang Daoling; Zhang Yulong; He Zhanjun

    2002-01-01

    14 C-lidocaine was composed by 14 C-diethylamine reaction with ω-chloroacetic-2,6-dimethylaniline. 14 C-diethylamine was prepared from Ba 14 CO 3 via K 14 CN and 14 C-acetonitrile which was hydrogenated. Radiochemical purity of 14 C-diethylamine and 14 C-lidocaine is >99% by HPLC and TLC respectively. 14 C-lidocaine is needed for breath assay of mouse for measuring liver function

  12. Degradation and residues of trifluralin and metalaxyl in soils treated with 14C-trifluralin and 14C-metalaxyl, under laboratory conditions

    International Nuclear Information System (INIS)

    Musumeci, M.R.; Ruegg, E.F.

    1986-01-01

    The behavior of the herbicide 14 C-trifluralin and the fungicide 14 C-metalaxyl was studied under laboratory conditions in Red Latosol and Yellow Red Podzol soils in samples Kept flooded, sterilized and with humidity equivalent to 60% of the water field capacity. The degradation of both pesticides is discussed. (M.A.C.) [pt

  13. Radiolytic decomposition of organic C-14 released from TRU waste

    International Nuclear Information System (INIS)

    Kani, Yuko; Noshita, Kenji; Kawasaki, Toru; Nishimura, Tsutomu; Sakuragi, Tomofumi; Asano, Hidekazu

    2007-01-01

    It has been found that metallic TRU waste releases considerable portions of C-14 in the form of organic molecules such as lower molecular weight organic acids, alcohols and aldehydes. Due to the low sorption ability of organic C-14, it is important to clarify the long-term behavior of organic forms under waste disposal conditions. From investigations on radiolytic decomposition of organic carbon molecules into inorganic carbonic acid, it is expected that radiation from TRU waste will decompose organic C-14 into inorganic carbonic acid that has higher adsorption ability into the engineering barriers. Hence we have studied the decomposition behavior of organic C-14 by gamma irradiation experiments under simulated disposal conditions. The results showed that organic C-14 reacted with OH radicals formed by radiolysis of water, to produce inorganic carbonic acid. We introduced the concept of 'decomposition efficiency' which expresses the percentage of OH radicals consumed for the decomposition reaction of organic molecules in order to analyze the experimental results. We estimated the effect of radiolytic decomposition on the concentration of organic C-14 in the simulated conditions of the TRU disposal system using the decomposition efficiency, and found that the concentration of organic C-14 in the waste package will be lowered when the decomposition of organic C-14 by radiolysis was taken into account, in comparison with the concentration of organic C-14 without radiolysis. Our prediction suggested that some amount of organic C-14 can be expected to be transformed into the inorganic form in the waste package in an actual system. (authors)

  14. Studies on residues of 14C malathion in soils

    International Nuclear Information System (INIS)

    Ghezal, F.; Bennaceur, M.

    1991-04-01

    The extractability, the mobility and formation of bound 14C labelled residues in two soils under normal conditions were investigated with malathion. Comparison is made between irradiated and autoclaved soils. The highest concentration of the product is found in the first section (0-4cm) after experiment. Three compounds were found in the soils. 14C malathion is decomposed to 14C02. The degradation is more important in organic matter rich soil. In rich soil, 50% of 14C product is degradated after 17 days. This percentage is only 10%, for poor soil. The 14CO 2 produced in non-sterile soil is 33,05%. This percentage is respectively 10,92% and 3,57% only for irradiated and autoclaved soils

  15. Syntheses of {gamma}-aminobutyric-1-{sup 14}C and of {alpha}-aminoadipic-6-{sup 14}C acid from methoxy-3 chloropropyl-magnesium and marked carbon dioxide; Syntheses de l'acide {gamma}-aminobutyrique{sup 14}C-1 et de l'acide {alpha}-aminoadipique {sup 14}C-6 a partir de methoxy-3 chloropropylmagnesium et d'anhydride carbonique marque

    Energy Technology Data Exchange (ETDEWEB)

    Liem, Phung Nhu [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires, Departement des radioelements, Service des molecules marquees

    1967-04-01

    Carbonation of {gamma}-methoxypropyl-magnesium chloride by CO{sub 2} gives {gamma}-methoxy-butyric carboxylic-{sup 14}C acid with a yield of about 95 per cent. When the latter is treated successively with anhydrous HBr and with diazomethane, methyl carboxylic {gamma}-bromobutyrate-{sup 14}C is formed. This in turn gives {gamma}-amino-butyric carboxylic-{sup 14}C acid with an overall yield of 66 per cent with respect to Ba{sup 14}CO{sub 3}, when it is condensed with potassium phthalimide and hydrolyzed by acid. By reacting methyl-{gamma}-bromobutyrate-{sup 14}C with the sodium derivative of ethyl cyanacetamido-acetate in ethanol, followed by an acid hydrolysis, {alpha}-aminoadipic-6-{sup 14}C acid is obtained with an overall yield of 46 per cent with respect to Ba{sup 14}CO{sub 3}. (author) [French] La carbonatation du chlorure de {gamma}-methoxypropylmagnesium par {sup 14}CO{sub 2} donne l'acide {gamma}-methoxybutyrique carboxyle {sup 14}C avec un rendement d'environ 95 pour cent. Ce dernier traite successivement par HBr anhydre et par le diazomethane conduit au {gamma}-bromobutyrate de methyle carboxyle {sup 14}C. Celui-ci condense avec le phtalimide de potassium suivi d'une hydrolyse acide fournit l'acide {gamma}-aminobutyrique carboxyle {sup 14}C avec un rendement global de 66 pour cent par rapport a Ba{sup 14}CO{sub 3}. L'action du {gamma}-bromobutyrate de methyle {sup 14}C sur le derive sode du cyanacetamidoacetate d'ethyle dans l'ethanol suivie d'hydrolyse acide donne l'acide {alpha}-aminoadipique {sup 14}C-6 avec un rendement global de 46 pour cent par rapport a Ba{sup 14}CO{sub 3}. (auteur)

  16. A novel stereospecific synthesis of 14C labeled 1-glutamic acid

    International Nuclear Information System (INIS)

    Wurz, R.E.; Kepner, R.E.; Webb, A.D.

    1989-01-01

    A stereospecific synthesis of 4- 14 C-1-glutamic acid was completed in five steps from sodium 2- 14 C-acetate. The morpholine derived enamine of ethyl pyruvate was reacted with ethyl 2- 14 C-bromoacetate to give after hydrolysis diethyl 4- 14 C-2-oxoglutarate. The 2-oxoglutarate was reacted with hydroxylamine hydrochloride to give diethyl 4-14C-2-hydroxyiminoglutarate which was then reduced with a LiAlH4, (-)-N-methylephedrine and 3,5-dimethylphenol mixture to give 4- 14 C-1-glutamic acid. The 4- 14 C-1-glutamic acid was used in investigations into the biosynthesis of gamma-lactones in sherries

  17. METABOLISM OF [14C]GA19 AND [14C]GA53 BY ECOTYPES OF ...

    African Journals Online (AJOL)

    ADMIN

    hand, metabolism of [14C]GA53 was very limited in all day-length treatments and during both, day and night periods. ... compounds which are formed by covalent coupling of GAs to .... For each ecotype day-time and night-time metabolism of ...

  18. Measurements of 14C in ancient ice from Taylor Glacier, Antarctica constrain in situ cosmogenic 14CH4 and 14CO production rates

    Science.gov (United States)

    Petrenko, Vasilii V.; Severinghaus, Jeffrey P.; Schaefer, Hinrich; Smith, Andrew M.; Kuhl, Tanner; Baggenstos, Daniel; Hua, Quan; Brook, Edward J.; Rose, Paul; Kulin, Robb; Bauska, Thomas; Harth, Christina; Buizert, Christo; Orsi, Anais; Emanuele, Guy; Lee, James E.; Brailsford, Gordon; Keeling, Ralph; Weiss, Ray F.

    2016-03-01

    Carbon-14 (14C) is incorporated into glacial ice by trapping of atmospheric gases as well as direct near-surface in situ cosmogenic production. 14C of trapped methane (14CH4) is a powerful tracer for past CH4 emissions from ;old; carbon sources such as permafrost and marine CH4 clathrates. 14C in trapped carbon dioxide (14CO2) can be used for absolute dating of ice cores. In situ produced cosmogenic 14C in carbon monoxide (14CO) can potentially be used to reconstruct the past cosmic ray flux and past solar activity. Unfortunately, the trapped atmospheric and in situ cosmogenic components of 14C in glacial ice are difficult to disentangle and a thorough understanding of the in situ cosmogenic component is needed in order to extract useful information from ice core 14C. We analyzed very large (≈1000 kg) ice samples in the 2.26-19.53 m depth range from the ablation zone of Taylor Glacier, Antarctica, to study in situ cosmogenic production of 14CH4 and 14CO. All sampled ice is >50 ka in age, allowing for the assumption that most of the measured 14C originates from recent in situ cosmogenic production as ancient ice is brought to the surface via ablation. Our results place the first constraints on cosmogenic 14CH4 production rates and improve on prior estimates of 14CO production rates in ice. We find a constant 14CH4/14CO production ratio (0.0076 ± 0.0003) for samples deeper than 3 m, which allows the use of 14CO for correcting the 14CH4 signals for the in situ cosmogenic component. Our results also provide the first unambiguous confirmation of 14C production by fast muons in a natural setting (ice or rock) and suggest that the 14C production rates in ice commonly used in the literature may be too high.

  19. Synthesis of carbon-14 analogue of 1,5 diaryl-5-[14C]-1,2,3-triazoles

    International Nuclear Information System (INIS)

    Matloubi, Hojatollah; Shafiee, Abbas; Saemian, Nader; Shirvani, Gholamhossein; Daha, Fariba Johari

    2004-01-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-methyl-phenyl)-1,2,3-triazole and 1-(4-methylsulfone-phenyl)-5-phenyl-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-tolunitrile-[cyano- 14 C] and benzonitrile-[cyano- 14 C], respectively

  20. Forensic applications of 14C bomb-pulse dating

    International Nuclear Information System (INIS)

    Zoppi, U.; Skopec, Z.; Skopec, J.; Jones, G.; Fink, D.; Hua, Q.; Jacobsen, G.; Tuniz, C.; Williams, A.

    2004-01-01

    After a brief review of the basics of 14 C bomb-pulse dating, this paper presents two unique forensic applications. Particular attention is dedicated to the use of the 14 C bomb-pulse to establish the time of harvest of illicit drugs such as heroin and opium. Preliminary measurements of 14 C concentrations in milligram samples taken from seized drugs are presented. 14 C bomb-pulse dating can determine whether drug distribution originates from stockpiles or recent manufacture, and support the action of law enforcement authorities against criminal organisations involved in drug trafficking. In addition, we describe the dating of wine vintages for a number of authenticated single label vintage red wines from the Barossa Valley - South Australia. Our results show that radiocarbon dating can be used to accurately determine wine vintages and therefore reveal the addition of unrelated materials of natural and synthetic origin

  1. Forensic applications of 14C bomb-pulse dating

    Science.gov (United States)

    Zoppi, U.; Skopec, Z.; Skopec, J.; Jones, G.; Fink, D.; Hua, Q.; Jacobsen, G.; Tuniz, C.; Williams, A.

    2004-08-01

    After a brief review of the basics of 14C bomb-pulse dating, this paper presents two unique forensic applications. Particular attention is dedicated to the use of the 14C bomb-pulse to establish the time of harvest of illicit drugs such as heroin and opium. Preliminary measurements of 14C concentrations in milligram samples taken from seized drugs are presented. 14C bomb-pulse dating can determine whether drug distribution originates from stockpiles or recent manufacture, and support the action of law enforcement authorities against criminal organisations involved in drug trafficking. In addition, we describe the dating of wine vintages for a number of authenticated single label vintage red wines from the Barossa Valley - South Australia. Our results show that radiocarbon dating can be used to accurately determine wine vintages and therefore reveal the addition of unrelated materials of natural and synthetic origin.

  2. A high resolution method for {sup 14}C analysis of a coral from South China Sea: Implication for “AD 775” {sup 14}C event

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Ping [State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 Guangzhou (China); Shen, Chengde, E-mail: cdshen@gig.ac.cn [State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 Guangzhou (China); State Key Laboratory of Nuclear Physics and Technology, Peking University, 100871 Beijing (China); Yi, Weixi; Wang, Ning [State Key Laboratory of Isotope Geochemistry, Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, 510640 Guangzhou (China); Ding, Xingfang; Liu, Kexin; Fu, Dongpo [State Key Laboratory of Nuclear Physics and Technology, Peking University, 100871 Beijing (China); Liu, Weiguo [State Key Laboratory of Loess and Quaternary Geology, Institute of Earth Environment, The Chinese Academy of Sciences, 710075 Xi’an (China); Liu, Yi [CAS Key Laboratory of Crust-Mantle Materials and Environments, School of Earth and Space Sciences, University of Science and Technology of China, 230026 Hefei (China)

    2015-10-15

    A pre-heating method that improves the background and precision of {sup 14}C dating significantly was applied for fossil coral dating with high resolution in our lab in Guangzhou Institute of Geochemistry, Chinese Academy of Sciences (GIGCAS). The reaction tube is heated under 300 °C in a vacuum line before it is used for graphitization. The method can reduce the contamination absorbed in TiH{sub 2}, Zn and Fe power placed in the graphitization tube. With the pre-heating and average drilling method, bi-weekly resolution {sup 14}C dating in a fossil coral is carried out to investigate the “AD 775 {sup 14}C spike event”. Different from the tree ring {sup 14}C archives with the {sup 14}C spike of ∼15‰ (Δ{sup 14}C), the {sup 14}C spike in the coral shows an abrupt peak of 45‰ and two smaller spikes of Δ{sup 14}C > 20‰ in half a year in AD 776. And then, the {sup 14}C content in coral decreases gradually in AD 777. The peak time of the {sup 14}C spike event likely occurs in the summer of AD 776 according to the δ{sup 18}O variation in coral. High-resolution dating of {sup 14}C in coral provides not only a more detail process of the event than that from tree rings, but also the first report of the event from sea ecosystem. Both of them suggest an extraterrestrial origin of the event cause.

  3. Placental transfer of 14C-hexoprenaline

    International Nuclear Information System (INIS)

    Lipshitz, J.; Broyles, K.; Whybrew, W.D.; Ahokas, R.A.; Anderson, G.D.

    1982-01-01

    The placental transfer of a single intravenous injection of 14 C-hexoprenaline was studied in eight pregnant New Zealand white rabbits. Maternal and fetal blood was sampled intermittently for 60 minutes after the injection. An initial rapid decrease in the levels of 14 C-hexoprenaline in maternal blood was followed by a second slower phase, whereas fetal heart rate after the administration of a single maternal intravenous injection of hexoprenaline in the treatment of fetal distress is due to the action on the uterus and/or on maternal cardiovascular function, and not to direct stimulation of the fetus

  4. BIOADSORCIÓN DE ARSÉNICO (III EN SOLUCIÓN ACUOSA POR LA BIOMASA MODIFICADA DE Aspergillus niger

    Directory of Open Access Journals (Sweden)

    Erik E. Santos

    2017-01-01

    Full Text Available Se analizó la capacidad de remoción de As (III en solución acuosa por la biomasa modificada de Aspergillus niger, mediante Espectrometría de Absorción Atómica. La mayor bioadsorción (66% con 1 mg/L del metaloide fue a las 24 horas, a pH de 6.0, 28oC y 1 g de biomasa modificada. Con respecto a la temperatura, la más alta remoción fue a los 28oC, con un 66% de remoción a las 24 horas. A las concentraciones de As (III analizadas, la biomasa mostró una buena capacidad de remoción. Al aumentar la concentración del bioadsorbente, la remoción es más eficiente (91.2% con 5 g de biomasa, además de remover eficientemente el metaloide (67% de remoción en agua natural contaminada con 1 mg/100 mL de As (III a las 24 horas con 5 g de biomasa, por lo que puede ser utilizado para eliminar aguas residuales industriales.

  5. {sup 14}C-Methylenebisphenylisocyanate ({sup 14}C-MDI). Study of absorption after single dermal and intradermal administration in rats

    Energy Technology Data Exchange (ETDEWEB)

    Leibold, E.; Hoffmann, H.D.; Hildebrand, B

    1999-07-01

    The absorption, distribution and excretion of radioactivity was studied in groups of four male Wistar rats following a single dermal and intradermal administration of {sup 14}C- Methylenebisphenylisocyanate ({sup 14}C-MDI) at nominal dose levels of 4.0 and 0.4 mg/cm{sup 2} for dermal administration and 0.4 mg/animal for intradermal administration. These dose levels nominally corresponded to 40 and 4.0 mg/animal for dermal administration. Considering the animal weights, dose levels corresponded to about 140 and 14 mg/kg body weight (dermal administration) and 1.4 mg/kg body weight (intradermal administration). In the experiments with dermal administration, animals were exposed for 8 hours and sacrificed 8, 24 or 120 h after beginning of exposure. In the experiment with intradermal administration, animals were sacrificed 120 h after treatment. After dermal administration of {sup 14}C-MDI, mean recoveries of radioactivity from all dose groups were in the range from 97.86 to 108.07% of the total radioactivity administered. Generally, the largest proportion of radioactivity was found at the application site and dressing. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) increased with increasing sacrifice time. Dermal absorption was very low and quantitatively similar at both dose levels; maximally ca. 0.9 % of the applied radioactivity was absorbed. After intradermal administration of {sup 14}C-MDI, the mean recovery of radioactivity was 100.90 % of the radioactivity administered. The largest proportion of radioactivity was found at the application site. The total amount of radioactivity absorbed (including excreta, cage wash, tissues/organs and carcass) amounted to about 26 % of the radioactivity applied. Irrespective of the mode of administration of 1{sup 4C}-MDI, concentrations of radioactivity in tissues and organs generally were below 1 {mu}g Eq/g at 120 h after administration. In summary, the results of this

  6. Synthesis of two 14C-labeled catechol-o-methyltransferase inhibitors

    International Nuclear Information System (INIS)

    Karlsson, Carita; Honkanen, Erkki

    1991-01-01

    14 C-labelled 3-(3,4-dihydroxy-5-nitrophenylmethylidene)-2,4-pentanedione and 14 C-labelled E-N,N-diethyl-2-cyano-3-(3,4-dihydroxy-5-nitrophenyl)acrylamide have been synthesized from [carbonyl- 14 C]vanillin. (author)

  7. Synthesis of organic substances labelled with 14C and 35S

    International Nuclear Information System (INIS)

    Pichat, L.

    1958-01-01

    After a brief history of the development of the Section des Molecules marquees of the French Atomic Energy Commission, the author gives an outline of the synthesis of the following labelled compounds: benzene 14 C-6; phenyl-p-fluorophenyl, thienyl-2 β alanines β 14 C; noradrenaline β 14 C (arterenol β 14 C), dotriacontane 14 C-16-17, aminoethane sulfinic acid (hypotaurine 35 S). (author) [fr

  8. [14C]Fluciclovine (alias anti-[14C]FACBC) uptake and ASCT2 expression in castration-resistant prostate cancer cells

    International Nuclear Information System (INIS)

    Ono, Masahiro; Oka, Shuntaro; Okudaira, Hiroyuki; Nakanishi, Takeo; Mizokami, Atsushi; Kobayashi, Masato; Schuster, David M.; Goodman, Mark M.; Shirakami, Yoshifumi; Kawai, Keiichi

    2015-01-01

    Introduction: trans-1-Amino-3-[ 18 F]fluorocyclobutanecarboxylic acid ([ 18 F]fluciclovine, also known as anti-[ 18 F]FACBC), is a tracer for positron emission tomography (PET) imaging for detection of tumors such as prostate cancer (PCa). Our previous study showed that ASCT2 (Na + -dependent amino acid transporter (AAT)) mediates fluciclovine uptake in androgen-dependent PCa cells; its expression is influenced by androgen, a key hormone in the progression of primary PCa and castration-resistant prostate cancer (CRPC). In this study, we investigated the uptake mechanisms and feasibility of [ 18 F]fluciclovine for CRPC in the androgen-dependent PCa cell line LNCaP and LNCaP-derivatives LNCaP-SF and LN-REC4. Methods: LNCaP-SF was established after long-term cultivation of LNCaP in steroid-free conditions, and LN-Pre and LN-REC4 were established from LNCaP inoculated in intact and castrated severe combined immunodeficient mice, respectively. Uptake and competitive inhibition experiments were performed with trans-1-amino-3-fluoro[1- 14 C]cyclobutanecarboxylic acid ([ 14 C]fluciclovine) to characterize the involvement of AATs in androgen-dependent PCa (LNCaP and LN-Pre) and CRPC-like (LNCaP-SF and LN-REC4) cell lines. AAT expression was analyzed by Western blotting, and [ 14 C]fluciclovine uptake in androgen-dependent PCa and CRPC-like cell lines were investigated in the presence or absence of dihydrotestosterone (DHT). Results: The contribution of Na + -dependent AATs to [ 14 C]fluciclovine uptake in all cell lines was 88−98%, and [ 14 C]fluciclovine uptake was strongly inhibited by L-glutamine and L-serine, the substrates for Na + -dependent alanine-serine-cysteine (system ASC) AATs, in the presence of Na + . DHT enhanced ASCT2 expression in LNCaP, LN-Pre, and LN-REC4, but not in LNCaP-SF, and the responses of ASCT2 expression to DHT correlated with [ 14 C]fluciclovine uptake. Conclusions: System ASC, especially ASCT2, could play a major role in [ 14 C

  9. 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.

  10. Effect of endomycorrhizae on the bioavailability of bound 14C residues to onion plants from an organic soil treated with [14C]fonofos

    International Nuclear Information System (INIS)

    Nelson, S.D.; Khan, S.U.

    1990-01-01

    Uptake of bound 14 C residues from an organic soil treated with radiolabeled fonofos (O-ethyl S-phenyl ethylphosphonodithioate) by selected Glomus endomycorrhiza and onion roots was studied. The hyphae of endomycorrhizal associations were capable of removing 14 C residues from the soil and transporting them to onion plants. Bioavailability of soil-bound 14 C residues, as measured by 14 C residue content in onion, was increased 32 and 40% over that of nonmycorrhizal plants by hyphae of Glomus intraradices and Glomus vesiculiferium, respectively. The data suggest that under field conditions endomycorrhizal infection may greatly increase the bioavailability of soil-bound pesticide residues to plants

  11. 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.

  12. Metabolism of 14C-L-arginine and 14C-L-proline in excised burst buds and stem sections of citrus trees (Citrus unshiu Marc.)

    International Nuclear Information System (INIS)

    Kato, Tadashi; Yamagata, Makoto; Tsukahara, Sadao

    1985-01-01

    Arginine and proline, which are the major forms of soluble reserve N, were fed singly in uniformly labelled 14 C-form to excised 2-year-old stem sections with a new shoot, to wood sections, and to burst buds from a 21-year-old satsuma mandarin tree. Metabolism was studied by radioassay and autoradiography. In stem sections with a new shoot, both 14 C-compounds were metabolized to acidic and neutral components, insoluble components, and 14 CO 2 . This conversion occurred to a greater extent in sections fed with arginine than with proline. When 14 C-arginine was fed, the highest 14 C-activity in the cationic fraction of stem sections, bark, wood and new shoots was found in γ-guanidinobutyric acid, followed by γ-aminobutyric acid and proline; low levels of 14 C was also found in ornithine and trace amounts in citrulline. These findings demonstrate that arginine is metabolized by at least two routes: via ornithine and via γ-guanidinobutyric acid. In every organ, the major metabolic products of 14 C-proline were pyrrolidone-5-carboxlic acid, glutamic acid, aspartic acid, asparagine, an unidentified compound (U 5 in Fig. 4), γ-aminobutyric acid and arginine. The basic metabolic pathways in the conversion of Both 14 C-compounds were the same in burst buds, new shoot, bark and wood, although there was a slight difference autoradiographically. (author)

  13. The use of 14C ethanolamine as a precursor

    International Nuclear Information System (INIS)

    Madelmont, J.C.; Parry, D.; Godeneche, D.; Duprat, J.

    1985-01-01

    Two new 2 chloroethyl nitrosoureas were labelled on two positions by 14 C starting from Na 14 CN and using 14 C ethanolamine as intermediate, i.e. on the carbon 2 of the 2 chloro ethyl group and on the carbon 2 of the cysteamine part. (author)

  14. Anaerobic C1 metabolism of the O-methyl-14C-labeled substituent of vanillate

    International Nuclear Information System (INIS)

    Frazer, A.C.; Young, L.Y.

    1986-01-01

    The O-methyl substituents of aromatic compounds constitute a C 1 growth substrate for a number of taxonomically diverse anaerobic acetogens. In this study, strain TH-001, an O-demethylating obligate anaerobe, was chosen to represent this physiological group, and the carbon flow when cells were grown on O-methyl substituents as a C 1 substrate was determined by 14 C radiotracer techniques. O-[methyl- 14 C]vanillate (4-hydroxy-3-methoxy-benzoate) was used as the labeled C 1 substrate. The data showed that for every O-methyl carbon converted to [ 14 C]acetate, two were oxidized to 14 CO 2 . Quantitation of the carbon recovered in the two products, acetate and CO 2 , indicated that acetate was formed in part by the fixation of unlabeled CO 2 . The specific activity of 14 C in acetate was 70% of that in the O-methyl substrate, suggesting that only one carbon of acetate was derived from the O-methyl group. Thus, it is postulated that the carboxyl carbon of the product acetate is derived from CO 2 and the methyl carbon is derived from the O-methyl substituent of vanillate

  15. Incorporation of U-/sup 14/C-glucose into the lipids U-/sup 14/C and sugars of Culex pipiens fatigans

    Energy Technology Data Exchange (ETDEWEB)

    Duggal, Rita Nanda; Subrahmanyam, D

    1983-11-01

    The role of U-/sup 14/C-glucose as a lipogenic precursor was examined in larvae and adults of C. pipiens fatigans. The pattern of incorporation of the radiocarbon was also examined in the sugars of these insects. It was found that on feeding of larvae and adults with /sup 14/C-glucose, the phospholipid fraction of the insects was associated with more than 70 per cent of the total lipid radiolabel. However, the percentage distribution of the phospholipid label in the different phospholipid fractions of the larvae and adults was different. Among the neutral lipids, a low but significant label in cholesterol was of considerable interest. The /sup 14/C-glucose was also converted to trehalose in both larvae and adults. However, the two stages differed in the utilization of glucose and trehalose. 5 figures, 16 refs.

  16. Synthesis of specific labelled [methyl-14C]sarin

    International Nuclear Information System (INIS)

    Sin-Ren, A.C.; Riggio, G.; Hopff, W.H.; Waser, P.G.

    1988-01-01

    The synthesis of [methyl- 14 C]sarin ([ 14 C]methylphosphono-fluoridic acid 1-methylethyl ester) was accomplished by another approach as for nonlabelled sarin in a tele-conducted reaction vessel. The purity was estimated by IR, GC, and GC-MS and the stability in different media was examined. (author)

  17. Monitoring of the 14C activity in the atmosphere

    International Nuclear Information System (INIS)

    Svingor, E.; Molnar, M.; Futo, I.; Rinyu, L.

    2006-01-01

    Complete text of publication follows. The distribution of atmospheric radiocarbon has been extensively investigated both in the Northern and Southern Hemisphere as well as in the Tropics for a number of decades. Systematic global observations of 14 CO 2 in the troposphere were made during and after atmospheric nuclear weapon tests in the 1950s and 1960s by several laboratories. Nowadays the monitoring of 14 C in regions adjacent to nuclear power plants (NPP) or sites of land-filled radioactive wastes has growing importance in determining the frequency and activity of anthropogenic 14 C released to the environment. On the other hand, the depletion of 14 C in the atmosphere gives information about the regional fossil fuel CO 2 contributions (Figure 1., Prague-Bulovka). The 14 C activity of the atmosphere has been monitored in the vicinity of Paks NPP by sampling environmental air monthly since 1994. Four differential sampling units collect air samples less than 2 km away from the 100- m-high stacks of Paks NPP (A-type stations), and for reference a sampler is operated at a station (B24) ca. 30 km away from Paks NPP. The highest 14 C values were measured at the site located less than 1km away from Paks NPP. The influence of the 14 C discharge in the environment decreases rapidly with the distance from the source and under normal operating conditions the effect of Paks NPP is negligible at a distance of 2.5km. In Figure 1. we have compared our data for Paks NPP measured during the time span of 2000 - 2005 with data from different European monitoring stations. (The 14 C activities are given in Δ values: Δ 14 C(% (A sample /A standard -1) x 1000.) In 2000-2001 the excess 14 C at Paks NPP compared to the B24 was 5-10 (per mille) but its Δ value didn't exceed the tropospheric background (1). With the growing traffic the inactive CO 2 emission (Suess effect) exceeded the influence of the NPP (2). After a cleaning tank incident at unit 2 of Paks NPP in April 2003 a 5

  18. Anthropogenic 14C in the natural (aquatic) environment

    International Nuclear Information System (INIS)

    Begg, F.H.

    1992-11-01

    Increasing global awareness of the radiological significance of 14 C releases from the nuclear and radiochemical industries has resulted in a number of studies within the last decade investigating the atmospheric releases and their effect on the terrestrial biosphere. The basis of this study was to determine the behaviour and environmental distribution of anthropogenically produced 14 C released to the aquatic environment from the nuclear fuel reprocessing plant at Sellafield. Most sampling was undertaken in the Irish Sea with smaller scale studies being carried out in the Bristol Channel and the Grand Union Canal. Within the study area, from Earnse Point 40 km south of Sellafield, northwards to the Clyde Sea area, preliminary studies on intertidal biota samples ie. mussels, winkles and seaweed indicated enriched 14 C specific activities in all the samples relative to the current ambient level of 115.4 pM. The highest activities were observed in the immediate vicinity of the discharge location; mussels with a measured activity of 787 pM, winkles of 613 pM and seaweed of 415 pM. The 14 C specific activity observed at most sites appeared to be organism dependent with mussels>winkles>seaweed. This is the result of differences in the uptake mechanisms of the organisms and indicates that the dissolved inorganic carbon and the particulate material within the water column are enriched in 14 C . However, on analysis of the biogeochemical fractions of the water column, enriched 14 C activities were observed only in the DIC fraction which could explain those activities found in the seaweed but not those in the mussels and winkles. Enriched 14 C activities were found in the phytoplankton, indicating that there is a source of enriched organic particulate material within the water column as a result of photosynthetic uptake of enriched DIC, however this will be a seasonal effect. Nevertheless, this enrichment is still not high enough to support the activities observed in the

  19. Synthesis of methyl-2 O-tolyl-3 quinazolone-4 {sup 14}C-2; Synthese de la methyl-2 O-tolyl-3 quinazolone-4 {sup 14}C-2

    Energy Technology Data Exchange (ETDEWEB)

    Herbert, M; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    Description of the preparation of methyl-2 O-tolyl-3 quinazolone-4 {sup 14}C-2 (abbreviated to M.T.Q.), using N-acetyl {sup 14}C-1 anthranilic acid. The overall yield reaches 72 per cent with respect to acetyl chloride {sup 14}C-1. By applying the same method to acetyl chloride {sup 14}C-2, M.T.Q. labelled on the methyl group could be obtained. (author) [French] Description de la preparation de la methyl-2 O-tolyl-3 quinazolone-4 {sup 14}C-2 (abregee en M.T.Q.) par l'intermediaire de l'acide N-acetyl {sup 14}C-1 anthranilique. Le rendement global atteint 72 pour cent par rapport au chlorure d'acetyle {sup 14}C-1. La meme methode appliquee au chlorure d'acetyle {sup 14}C-2 permettrait d'obtenir la M.T.Q. marquee sur le groupement methyle. (auteur)

  20. Preparation of 14-C-labelled 1,4-Dideoxy-1,4-imino-D-arabinitol: Cyanosilylation of Cyclic Imines using KCN in a One-Pot Synthesis

    DEFF Research Database (Denmark)

    Lundt, Inge; Malle, Birgitte Mølholm; Foged, Christian

    1999-01-01

    A new method for C-C bond formation was developed based on in situ cyanosilylation of cyclic Schiff bases using KCN, TMSCl, KI and ZnI2. This method was used to prepare the potent -glucosidase inhibitor 1,4-dideoxy-1,4-imino-D-arabinitol 14-C labelled at C-5.Keywords: in situ cyanosilylation; 14-C...

  1. Placental transfer of 14C-hexoprenaline

    International Nuclear Information System (INIS)

    Lipshitz, J.; Broyles, K.; Whybrew, W.D.; Ahokas, R.A.; Anderson, G.D.

    1982-01-01

    The placental transfer of a single intravenous injection of 14C-hexoprenaline was studied in eight pregnant New Zealand white rabbits. Maternal and fetal blood was sampled intermittently for 60 minutes after the injection. An initial rapid decrease in the levels of 14C-hexoprenaline in maternal blood was followed by a second slower phase, whereas fetal levels remained insignificant. The conclusion, therefore, is that the rapid improvement in fetal heart rate after the administration of a single maternal intravenous injection of hexoprenaline in the treatment of fetal distress is due to the action on the uterus and/or on maternal cardiovascular function, and not to direct stimulation of the fetus

  2. TMEM14C is required for erythroid mitochondrial heme metabolism.

    Science.gov (United States)

    Yien, Yvette Y; Robledo, Raymond F; Schultz, Iman J; Takahashi-Makise, Naoko; Gwynn, Babette; Bauer, Daniel E; Dass, Abhishek; Yi, Gloria; Li, Liangtao; Hildick-Smith, Gordon J; Cooney, Jeffrey D; Pierce, Eric L; Mohler, Kyla; Dailey, Tamara A; Miyata, Non; Kingsley, Paul D; Garone, Caterina; Hattangadi, Shilpa M; Huang, Hui; Chen, Wen; Keenan, Ellen M; Shah, Dhvanit I; Schlaeger, Thorsten M; DiMauro, Salvatore; Orkin, Stuart H; Cantor, Alan B; Palis, James; Koehler, Carla M; Lodish, Harvey F; Kaplan, Jerry; Ward, Diane M; Dailey, Harry A; Phillips, John D; Peters, Luanne L; Paw, Barry H

    2014-10-01

    The transport and intracellular trafficking of heme biosynthesis intermediates are crucial for hemoglobin production, which is a critical process in developing red cells. Here, we profiled gene expression in terminally differentiating murine fetal liver-derived erythroid cells to identify regulators of heme metabolism. We determined that TMEM14C, an inner mitochondrial membrane protein that is enriched in vertebrate hematopoietic tissues, is essential for erythropoiesis and heme synthesis in vivo and in cultured erythroid cells. In mice, TMEM14C deficiency resulted in porphyrin accumulation in the fetal liver, erythroid maturation arrest, and embryonic lethality due to profound anemia. Protoporphyrin IX synthesis in TMEM14C-deficient erythroid cells was blocked, leading to an accumulation of porphyrin precursors. The heme synthesis defect in TMEM14C-deficient cells was ameliorated with a protoporphyrin IX analog, indicating that TMEM14C primarily functions in the terminal steps of the heme synthesis pathway. Together, our data demonstrate that TMEM14C facilitates the import of protoporphyrinogen IX into the mitochondrial matrix for heme synthesis and subsequent hemoglobin production. Furthermore, the identification of TMEM14C as a protoporphyrinogen IX importer provides a genetic tool for further exploring erythropoiesis and congenital anemias.

  3. 14C Analysis of protein extracts from Bacillus spores.

    Science.gov (United States)

    Cappuccio, Jenny A; Falso, Miranda J Sarachine; Kashgarian, Michaele; Buchholz, Bruce A

    2014-07-01

    Investigators of bioagent incidents or interdicted materials need validated, independent analytical methods that will allow them to distinguish between recently made bioagent samples versus material drawn from the archives of a historical program. Heterotrophic bacteria convert the carbon in their food sources, growth substrate or culture media, into the biomolecules they need. The F(14)C (fraction modern radiocarbon) of a variety of media, Bacillus spores, and separated proteins from Bacillus spores was measured by accelerator mass spectrometry (AMS). AMS precisely measures F(14)C values of biological materials and has been used to date the synthesis of biomaterials over the bomb pulse era (1955 to present). The F(14)C of Bacillus spores reflects the radiocarbon content of the media in which they were grown. In a survey of commercial media we found that the F(14)C value indicated that carbon sources for the media were alive within about a year of the date of manufacture and generally of terrestrial origin. Hence, bacteria and their products can be dated using their (14)C signature. Bacillus spore samples were generated onsite with defined media and carbon free purification and also obtained from archived material. Using mechanical lysis and a variety of washes with carbon free acids and bases, contaminant carbon was removed from soluble proteins to enable accurate (14)C bomb-pulse dating. Since media is contemporary, (14)C bomb-pulse dating of isolated soluble proteins can be used to distinguish between historical archives of bioagents and those produced from recent media. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

  4. Diagnóstico prenatal citogenético mediante amniocentesis durante los trimestres II y III de gestación en Costa Rica

    Directory of Open Access Journals (Sweden)

    Isabel Castro Volio

    2001-12-01

    Full Text Available El objetivo de este estudio fue identificar cromosomopatía fetal en voluntarias con embarazos de alto riesgo genético, brindar adecuada atención obstétrica y pediátrica y asesoramiento genético. En 842 embarazadas se obtuvo células fetales mediante amniocentesis, realizadas desde 1986 hasta 1999 inclusive. Las punciones se realizaron en hospitales del sistema de seguridad social y en la consulta privada. La indicación del 48 % de las amniocentesis fue el examen ultrasonográfico anormal y el 35 % de las punciones fue por edad materna avanzada. El 66 % de las veces el estudio se realizó en el II trimestre del embarazo y el 34 % en el III trimestre. Se utilizó el sistema cerrado de histocultivo y la cosecha por suspensión. El resultado final se obtuvo en 14 días (mediana. De las 842 muestras de líquido amniótico, en 217 no fue posible obtener resultados. Los 625 cariotipos fetales fueron anormales en 55 casos (9 %: 33 cariotipos trisómicos (incluyendo una trisomía 13 por translocación Robertsoniana de los cromosomas 13 y 14, ocho casos con síndrome de Turner (45,X, tres mosaicos cromosómicos (incluyendo una trisomía 22 en mosaico y 11 cariotipos anormales por otras causas. Al comparar la cantidad de defectos cromosómicos en relación a la indicación para efectuar la amniocentesis, se encontró un 17 % de cromosomopatía en los casos estudiados por ultrasonograma anormal y 2.5 % en los casos investigados por razón de la edad materna. En el seguimiento de 211 casos se encontró concordancia entre el cariotipo y el fenotipo del recién nacido, al igual que entre el diagnóstico ultrasonográfico fetal y la condición del neonato. El diagnóstico prenatal de cromosomopatía permitió el asesoramiento genético y el manejo obstétrico y pediátrico de los casos de manera adecuada. En los embarazos con cariotipo normal, esta información alivió la preocupación de muchos de los padresThe identification of fetal abnormal

  5. Nucleotide sequence of a cDNA coding for the amino-terminal region of human prepro. alpha. 1(III) collagen

    Energy Technology Data Exchange (ETDEWEB)

    Toman, P D; Ricca, G A [Rorer Biotechnology, Inc., Springfield, VA (USA); de Crombrugghe, B [National Institutes of Health, Bethesda, MD (USA)

    1988-07-25

    Type III Collagen is synthesized in a variety of tissues as a precursor macromolecule containing a leader sequence, a N-propeptide, a N-telopeptide, the triple helical region, a C-telopeptide, and C-propeptide. To further characterize the human type III collagen precursor, a human placental cDNA library was constructed in gt11 using an oligonucleotide derived from a partial cDNA sequence corresponding to the carboxy-terminal part of the 1(III) collagen. A cDNA was identified which contains the leader sequence, the N-propeptide and N-telopeptide regions. The DNA sequence of these regions are presented here. The triple helical, C-telopeptide and C-propeptide amino acid sequence for human type III collagen has been determined previously. A comparison of the human amino acid sequence with mouse, chicken, and calf sequence shows 81%, 81%, and 92% similarity, respectively. At the DNA level, the sequence similarity between human and mouse or chicken type III collagen sequences in this area is 82% and 77%, respectively.

  6. The microdose rapid 14C urea breath test compares well with the original rapid 14 breath test

    International Nuclear Information System (INIS)

    Bellon, M.S.; Bartholomeusz, F.D.L.; Chatterton, B.E.

    2000-01-01

    Full text: The 14 C urea breath test (CUBT) is a sensitive test used in the detection of H. pylori infection. The rapid 14 CUBT using 185 KBq of 14 C urea showed a sensitivity of 100% when tested in 36 patients. The aim of this study was to compare the results of the 14 CUBT performed following the ingestion of 37KBq microdose 14 C urea capsule (Bicapsule, Trimed) with the earlier method which uses 185 KBq 14 C urea. 19 patients (nine female age 21-52 yrs) were studied. All subjects first underwent a 14 CUBT with the microdose capsule and a single 15 minute post ingestion sample. An hour later the test was repeated but with a dose of 185 KBq 14 C urea in liquid form. A normal result was taken as 2 = 0.92). This is shown above. The Rapid 14 CUBT performed following the microdose capsule whilst reducing patient radiation exposure is an accurate test for the detection of H. pylori. Copyright (2000) The Australian and New Zealand Society of Nuclear Medicine Inc

  7. Residues of 14C-paclobutrazol in mangoes

    International Nuclear Information System (INIS)

    Costa, Maria A.; Tornisielo, Valdemar L.; Castanho, Giuliane M.

    2009-01-01

    Paclobutrazol (PBZ) is a growth regulator used in agricultural systems whose purpose is the control of vegetative growth, stimulating the reproductive capacity of plants. This growth regulator remains active in soil for a long time and its half-life varies with the type of soil and climatic conditions, can severely affect the development of crops. This work aimed to study the residues / metabolites of 14 C-PBZ in mango pulp Tommy Atkins. The tests were performed with mangoes grown in pots stainless steel and application of 14 C-PBZ was performed by the soil projection of the crown, and the mangoes tested in two periods, one year and two years after application. To evaluate the levels of residues of 14 C-PBZ was realize the burning of 200 mg of pulp on biological oxidized and detached 14 CO 2 was detected by liquid scintillation spectrophotometer. The results were 1.65 % of residue of PBZ on fruit collected after two years of application and 4.30 % of residue of PBZ collected on fruit after a year of application and also can see that the product remained in the soil for more than one year, is translocated to the plant and reach the edible part, the pulp fruit. The identification of residual 14 C- PBZ/metabolites by thin-layer chromatography did not reveal any pattern of PBZ / metabolites due to the low activity detected in the samples. Therefore, another procedure was performed for extraction and then analyzed by high performance liquid chromatography (HPLC) for detection of metabolites in the PBZ of mango pulp. (author)

  8. Synthesis and characterization of 14C polyvinylphosphonic acid

    International Nuclear Information System (INIS)

    Stringer, O.D.; Charig, A.

    1989-01-01

    Ten mCi of 14 C ethylene was converted to 1.16 mCi of 14 C PVPA by oxidative phosphonation with phosphorus trichloride and molecular oxygen, dehydrohalogenation with triethylamine in ether, polymerization, and hydrolysis. The polymer had a specific activity of 12 uCi/mg and a radiochemical purity over 99%. (Author)

  9. Dating of groundwater with tritium and 14C

    International Nuclear Information System (INIS)

    Muennich, K.O.; Roether, W.; Thilo, L.

    1967-01-01

    Shallow groundwater can be dated with some accuracy on the basis of its bomb tritium content if the unsaturated soil cover and the aquifer itself is sufficiently homogeneous. A few examples from the Rhine valley are presented. The decrease in tritium level from the water table to a few metres below is nearly two orders of magnitude. Agreement between the measured or estimated variation of bomb tritium in rain during the past decade and the tritium found in shallow groundwater can be obtained if one takes into account that (a) practically no summer rain reaches the water table, and (b) water is mixed by diffusion. Both effects can also be observed in the soil moisture of the unsaturated soil above the water table. Carbon-14 increase in groundwater due to bombs is delayed compared to tritium, the reasons being delay in the biological system and exchange with the carbonate in the soil. Nevertheless lysimeters show a marked increase of 14 C, which depends on the plant cover, being high in a plant-covered lysimeter and low in a bare one. A simple model is presented, which allows the evaluation of the influence of exchange on the 14 C age obtained. It turns out that the deviation from the true age depends on the ratio of the carbonate content in the aquifer material to the carbonate content of the water, on the specific contact surface or the grain size but not on the groundwater velocity. On the basis of this model the experimental finding that 14 C ages are usually in agreement with other age estimates despite the loss by exchange is plausible owing to the fact that only material of sufficiently coarse grain size can make up a reasonable aquifer. Assuming only exchange with a monomolecular surface layer of the carbonate grains one finds that the 14 C age is likely to differ by not more than a factor of two in the most unfavourable case. Under natural conditions (steady state of cosmic-ray-produced 14 C) the 14 C content of shallow groundwater is hardly influenced at

  10. Synthesis of the muscle relaxant [14C]L-637,510

    International Nuclear Information System (INIS)

    O'Connor, S.P.; Ellsworth, R.L.; Gatto, G.

    1991-01-01

    The synthesis of (E)-3-(9-chloro-5,6-dihydro-11H-pyrolo(2,1-b)(3)-benzazepin-11-ylidene)-N,N-dimethyl-1- [3- 14 C]-propanamine (Z)-2-butenedioate(1:1) ([ 14 C]L-637,510), a potential muscle relaxant product for which 14 C-labeling was required for metabolism studies, is described. Introduction of the label in the 3-position of the propanamine side chain was accomplished in eight steps from sodium [ 14 C]cyanide with an overall radiochemical yield of 4.8%. (author)

  11. The effects of the oral administration of fish oil concentrate on the release and the metabolism of [14C]arachidonic acid and [14C]eicosapentaenoic acid by human platelets

    International Nuclear Information System (INIS)

    Hirai, A.; Terano, T.; Hamazaki, T.

    1982-01-01

    It has been suggested by several investigators that eicosapentaenoic acid (C20:5 omega 3, EPA) might have anti-thrombotic effects. In this experiment, the effect of the oral administration of EPA rich fish oil concentrate on platelet aggregation and the release and the metabolism of [ 1 - 14 C]arachidonic acid and [(U)- 14 C]eicosapentaenoic acid by human platelets was studied. Eight healthy male subjects ingested 18 capsules of fish oil concentrate (EPA 1.4 g) per day for 4 weeks. Plasma and platelet concentrations of EPA markedly increased, while those of arachidonic acid (C20:4 omega 6, AA) and docosahexaenoic acid (C22:6 omega 3, DHA) did not change. Platelet aggregation induced by collagen and ADP was reduced. Collagen induced [ 14 C]thromboxane B2 (TXB2) formation from [ 14 C]AA prelabeled platelets decreased. There was no detectable formation of [ 14 C]TXB3 from [ 14 C]EPA prelabeled platelets, and the conversion of exogenous [ 14 C]EPA to [ 14 C]TXB3 was lower than that of [ 14 C]AA to [ 14 C]TXB2. The release of [ 14 C]AA from [ 14 C]AA prelabeled platelets by collagen was significantly decreased. These observations raise the possibility that the release of arachidonic acid from platelet lipids might be affected by the alteration of EPA content in platelets

  12. Metabolism of L-[guanidinooxy-14C]canavanine in the rat

    International Nuclear Information System (INIS)

    Thomas, D.A.; Rosenthal, G.A.

    1987-01-01

    The metabolism of L-canavanine, a nonprotein amino acid with significant antitumor effects, was investigated. L-Canavanine, provided at 2.0 g/kg, was supplemented with 5 microCi of L-[guanidinooxy- 14 C]canavanine (58 microCi/mumol) and administered iv, sc, or orally to female Sprague-Dawley rats weighing approximately 200 g. 14 C recovery in the urine at 24 hr was 83, 68, or 61%, respectively, of the administered dose. Another 5-8% of the 14 C was expired as 14 CO 2 . The gastrointestinal tract contained 21% of orally administered 14 C. Serum, feces, tissues, and de novo synthesized proteins only accounted for a few percent of the original dose by any administrative route. Analysis of the 14 C-containing urinary metabolites revealed that [ 14 C] urea accounted for 88% of the urinary radioactivity for an iv injection, 75% for sc administration, and 50% following an oral dose. By all routes of administration, [ 14 C]guanidine represented 5% of the radioactivity in the urine and [ 14 C]guanidinoacetic acid accounted for 2%. Serum and urine amino acid analysis showed a markedly elevated ornithine level. Basic amino acids such as histidine, lysine, and arginine were also higher in the urine. Plasma ammonia levels were determined following oral canavanine doses of 1.0, 2.0, and 4.0 g/kg. A rapid but transient elevation in plasma ammonia was observed only at the 4.0 g/kg dose. This indicates that elevated plasma ammonia is not a likely cause of canavanine toxicity at the drug concentrations used in this study

  13. Working out microsyntheses for different chlorinated biphenyls and preparation of 2,2'-dichlorobiphenyl-14C and 2,4'-dichlorobiphenyl-14C

    International Nuclear Information System (INIS)

    Geuenich, H.H.

    1972-01-01

    The microsyntheses for the preparation of chlorated biphenyls starting with benzene were worked out. 2,2'-dichlorobiphenyl- 14 C and 2,4'-dichlorobiphenyl- 14 C were prepared. 42 mCi benzene- 14 C were converted into nitrobenzene with nitrating acid, which was reduced to aniline by tin(II) chloride/hydrochloric acid. Following the acetylation of aniline with acetic anhydride, it was monochlorated in glacial acetic acid with chloride of lime, and the chlorination mixture was chromatographically separated in columns. 5.8 mCi o'-chloroanaline were diazotized and converted in ammoniacal copper(I) salt solution. 2 μCi 2,2'-dichlorobiphenyl were obtained. (orig./LH) [de

  14. Rh(III)-Catalyzed Synthesis of N-Unprotected Indoles from Imidamides and Diazo Ketoesters via C-H Activation and C-C/C-N Bond Cleavage.

    Science.gov (United States)

    Qi, Zisong; Yu, Songjie; Li, Xingwei

    2016-02-19

    The synthesis of N-unprotected indoles has been realized via Rh(III)-catalyzed C-H activation/annulation of imidamides with α-diazo β-ketoesters. The reaction occurs with the release of an amide coproduct, which originates from both the imidamide and the diazo as a result of C═N cleavage of the imidamide and C-C(acyl) cleavage of the diazo. A rhodacyclic intermediate has been isolated and a plausible mechanism has been proposed.

  15. Root uptake of 14C leached from the low-level radioactive waste for sub-surface disposal with engineered barriers by Oryza sativa L. (2). Distribution of 14C in rice plant on the case using acetic acid as 14C-source

    International Nuclear Information System (INIS)

    Suzuki, Hiroyuki; Ishii, Nobuyoshi; Tagami, Keiko; Uchida, Shigeo

    2012-01-01

    The behavior of 14 C from radioactive waste in paddy rice (Oryza sativa L.) at different stages of plant development was studied using the hydroponic and acetic acid as 14 C-source. For 14 C-application, plant root was soaked for 2 hours in a nutrient solution containing 14 C-acetic acid at the vegetative growth stage (Aug. 2, 2007), heading (flowering) stage (Aug. 30, 2007) and milk-ripe stage (Sep. 13, 2007). In final sampling day (Mar. 5, 2008), 0.88 - 1.96% of the applied radioactivity was recovered from whole plant, however, the ratio of recovered radioactivity was not different at the growth stage. The distribution of 14 C absorbed at each stage to each organ was noted to be highest in the submersed root through all the stages. Therefore the mixing of the root residue at the time of plowing would result in enhancement of the soil persistence of 14 C. (author)

  16. IgE and IgG cross-reactivity among Lol p I and Lol p II/III. Identification of the C-termini of Lol p I, II, and III as cross-reactive structures.

    Science.gov (United States)

    van Ree, R; van Leeuwen, W A; van den Berg, M; Weller, H H; Aalberse, R C

    1994-04-01

    In this study, the homologous C-termini of Lol p I, Lol p II, and Lol p III were shown to contain cross-reactive B-cell epitopes. This was demonstrated by inhibition studies with purified Lol p I, II, and III and synthetic peptides of their C-termini. It was ruled out that the observed cross-reactivity was caused by cross-contamination of the purified allergens. Both human IgE and IgG bound to the C-terminus of Lol p I. These antibodies were cross-reactive with Lol p II and, more specifically, with its C-terminus. Within a small panel of allergic patients, no cross-reactivity with Lol p III was found. A hyperimmune polyclonal rabbit antiserum against Lol p I also recognized the Lol p I C-terminus. As for human antibodies, cross-reactivity with Lol p II and its C-terminus was demonstrated. Cross-reactivity with Lol p III was demonstrated with C-terminal peptides, but not with native Lol p III. A polyclonal rabbit antiserum against Lol p II bound to the C-terminal peptides of both Lol p II and III. This binding was inhibited with Lol p I, confirming that cross-reactive structures exist not only on the C-termini of Lol p II and Lol p I, but also of Lol p III and Lol p I. The existence of cross-reactivity between Lol p I and Lol p II and III possibly contributes to the frequently observed cosensitization for these allergens in grass-pollen-allergic patients.

  17. Rectal absorption of homatropine [14C] methylbromide in the rat

    International Nuclear Information System (INIS)

    Cramer, M.B.; Cates, L.A.; Clarke, D.E.

    1978-01-01

    Homatropine [ 14 C]methylbromide (HMB- 14 C) was administered to rats by intramuscular injection, oral gavage and rectal suppository. Plasma concentrations of 14 C were measured over the subsequent 12 h. Peak plasma concentrations were higher and achieved more rapidly after rectal administration than by other routes whether HMB- 14 C was administered in a water-soluble suppository base or in aqueous solution. Twelve h after the suppositories were inserted and retained 28% of the 14 C had been excreted in the urine while 56% remained in the large intestine. Unlabelled HMB, given in rectal suppositories to anaesthetized rats, caused prompt blockade of the effects of vagal stimulation on pulse rate and of intravenous acetylcholine on blood pressure. These results confirm the rapid rectal absorption of the drug. (author)

  18. Autoradiography of ( sup 14 C)paraquat or ( sup 14 C)diquat in frogs and mice: accumulation in neuromelanin

    Energy Technology Data Exchange (ETDEWEB)

    Lindquist, N G; Larsson, B S; Lyden-Sokolowski, A [Uppsala Univ., Biomedical Center, (Sweden). Dept. of Toxicology

    1988-10-31

    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 ({sup 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 ({sup 14}C)paraquat or({sup 14}C)diquat. By means of whole body autoradiography of ({sup 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.

  19. Synthesis of carbon-14 analogue of 1,5 diaryl-5-[{sup 14}C]-1,2,3-triazoles

    Energy Technology Data Exchange (ETDEWEB)

    Matloubi, Hojatollah E-mail: hmatloubi@aeoi.org.ir; Shafiee, Abbas; Saemian, Nader; Shirvani, Gholamhossein; Daha, Fariba Johari

    2004-05-01

    Two 1,2,3-triazole anticonvulsants, 1-(4-methylsulfone-phenyl)-5-(4-methyl-phenyl)-1,2,3-triazole and 1-(4-methylsulfone-phenyl)-5-phenyl-1,2,3-triazole, both labeled with carbon-14 in the 5-position were prepared from para-tolunitrile-[cyano-{sup 14}C] and benzonitrile-[cyano-{sup 14}C], respectively.

  20. Rarotonga Radiocarbon (delta 14C) for 1950 to 1997

    Data.gov (United States)

    National Oceanic and Atmospheric Administration, Department of Commerce — Rarotonga coral radiocarbon (14C) timeseries. Coral radiocarbon (Delta-14C) on untreated, low-speed drilled samples. Precision is +/- 4 per mil as documented by an...

  1. Practical synthesis of 14C S-ribosyl-L-homocysteine uniformly labelled on the sugar moiety. An enzymatic route from (U-14C) adenosine

    International Nuclear Information System (INIS)

    Guillerm, G.; Allart, B.

    1992-01-01

    [(U- 14 C) S-Ribosyl]-L-homocysteine has been prepared enzymatically from (U- 14 C) adenosine in two steps using S-adenosyl homocysteine hydrolase and bacterial S-adenosyl homocysteine nucleosidase as catalysts. (Author)

  2. From 14C/12C measurements towards radiocarbon dating of ice

    NARCIS (Netherlands)

    Oerlemans, J.; Wal, R.S.W. van de; Roijen, J.J. van; Raynaud, D.; Borg, K. van der; Jong, A.F.M. de; Lipenkov, V.; Huybrechts, P.

    1994-01-01

    A dry extraction method of CO2 included in glacier ice adds a contamination equivalent to 1.8 μg modern carbon for a 35 μg C sample. This enables radiocarbon dating by accelerator mass spectrometry of 35 μg C samples to about 25 000 BP. Measured 14C/12C ratios are presented for a part of the Vostok

  3. 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

  4. New applications of 14C measurements at the Lund AMS Facility

    International Nuclear Information System (INIS)

    Stenstroem, K.

    1995-11-01

    Some new applications of accelerator mass spectroscopy (AMS) with 14 C are presented. In the first part the sample preparation used for production of elemental carbon at the Lund AMS facility is described. The second part concerns the release of 14 C from nuclear power plants. In a one-year study, the total airborne discharge of 14 C from two Swedish reactors was measured. In another study, the fraction of 14 CO 2 of the total airborne 14 C release was determined. The third part of the thesis involves the use of 14 C in nuclear medicine. The long-term retention of 14 C-labelled triolein after a fat-malabsorption test has been investigated by means of AMS by analysis of expired CO 2 . The possibilities of using ultra-low amounts of activity for fat-malabsorption tests, employing AMS technique, is demonstrated. In the last part AMS and 14 C-labelled tracers are used in food chemistry studies of interactions between foods and packaging materials. 22 refs, 8 figs, 2 tabs

  5. AMS 14C measurements for tree-ring samples from Japanese woods from 4c AD to 8c AD

    International Nuclear Information System (INIS)

    Ozaki, Hiromasa; Sakamoto, Minoru; Imamura, Mineo; Mitsutani, Takumi

    2010-01-01

    Regional offsets of atmospheric 14 C concentration, as represented by differences from IntCal calibration datasets, are discussed at times in relation to universal use of international radiocarbon calibration curve. In the construction of IntCal, 14 C contents of contemporaneous tree-ring samples from different regions in the northern hemisphere have been used, because the regional differences were indistinguishable from errors of measurements. Nowadays, high-precision 14 C results can be obtained much more easily than before, so more attention should be paid to the possible regional offsets. Most parts of IntCal has been constructed by using 14 C contents of tree-ring samples from woods in high latitude of Europe and North America, which are farthest from Japan in the northern hemisphere. So far, we have measured 14 C contents of tree-ring samples from Japanese wood samples dendrochronologically dated from 11th century BC to 4th century AD in order to investigate regional offset in Japan. Although the obtained results agreed well with IntCal in general, there were some periods when the 14 C contents differ significantly from IntCal. In this paper, we report the new results of AMS 14 C measurement for Japanese tree-ring samples ranging from 4th century AD to 8th century AD. The results show a significant disagreement with IntCal at around 630 AD. Similar difference was indicated by 14 C contents of tree-ring samples from other Japanese woods (Imamura et al., 2007). So it is certain that the regional offset in Japan exists at around 630 AD. (author)

  6. Influence of a few composts on the mineralization of 14C phenmedipham in a fresh meadow soil and the immobilization of the 14C residues

    International Nuclear Information System (INIS)

    Bellinck, C.; Mayaudon, J.

    1983-01-01

    The influence of four composts on the mineralization of 14 C phenmedipham in a fresh soil and the distribution of 14 C phenmedipham and its 14 C residues after one year incubation were studied. Straw compost had an important positive effect on the degradation of the herbicide. After a negative influence during the 15 first days of incubation, composts of mushroombeds, grapes and oak-bark - hen-dung had little influence. The soils treated with these three last composts showed a more important complexation of 14 C than the control-soil or the soil treated with straw-compost. Calculation of the quantity of free 14 C substances in the soil after one year incubation gave for the four composts values comprised between 39 and 84% of that of the control [fr

  7. Effect of a few amendments on the mineralization of 14C phenmedipham in a fresh meadow soil and the immobilization of the 14C residues

    International Nuclear Information System (INIS)

    Bellinck, C.

    1983-01-01

    The influence of a few amendments on the mineralization of 14 C phenmedipham in a fresh soil and the distribution of 14 C phenmedipham and its 14 C residues after one year incubation were studied. The N and NPK fertilizers, glucose, cellulose and amorphous calcic humates had a positive effect on the mineralization of the herbicide. Straw, NAFS extract and amorphous lignin had little influence while colloidal lignin and colloidal calcic humates had a negative effect on the mineralization. All the amendments tested increased the quantity of 14 C substances fixed on the soil constituents and so decreased pollution. Calculation of the quantity of free 14 C in the soil after one year incubation showed for the various amendments values comprised between 56 and 93% of that of the control [fr

  8. 14C measurements in aquifers with methane

    International Nuclear Information System (INIS)

    Barker, J.F.; Fritz, P.; Brown, R.M.

    1978-01-01

    A survey of various groundwater systems indicates that methane is a common trace constituent and occasionally a major carbon species in groundwaters. Thermocatalytic methane had delta 13 CCH 4 > -45% 0 and microbially-produced or biogenic methane had delta 13 CCH 4 0 . Groundwaters containing significant biogenic methane had abnormally heavy delta 13 C values for the inorganic carbon. Thermocatalytic methane had no apparent effect on the inorganic carbon. Because methanogenesis seriously affects the carbon isotope geochemistry of groundwaters, the correction of raw 14 C ages of affected groundwaters must consider these effects. Conceptual models are developed which adjust the 14 C activity of the groundwater for the effects of methanogenesis and for the dilution of carbon present during infiltration by simple dissolution of rock carbonate. These preliminary models are applied to groundwaters from the Alliston sand aquifer where methanogenesis has affected most samples. In this system, methanogenic bacteria using organic matter present in the aquifer matrix as substrate, have added inorganic carbon to the groundwater which has initiated further carbonate rock dissolution. These processes have diluted the inorganic carbon 14 C activity. (orig.) [de

  9. Processing of indium (III solutions via ion exchange with Lewatit K-2621 resin

    Directory of Open Access Journals (Sweden)

    López Díaz-Pavón, Adrián

    2014-06-01

    Full Text Available The processing of indium(III-hydrochloric acid solutions by the cationic ion exchange Lewatit K-2621 resin has been investigated. The influence of several variables such as the hydrochloric acid and metal concentrations in the aqueous solution and the variation of the amount of resin added has been studied. Moreover, a kinetic study performed in the uptake of indium(III by Lewatit K-2621, shows that either the film-diffusion and the particle-diffusion models fit the ion exchange process onto the resin, depending upon the initial metal concentration in the aqueous solution. The loaded resin could be eluted by HCl solutions at 20 °C.Se ha investigado el tratamiento de disoluciones de ácido clorhídrico conteniendo indio(III mediante la resina de cambio catiónico Lewatit K-2621. Las variables ensayadas han sido las concentraciones de ácido y de metal en la disolución acuosa y la cantidad de resina empleada en el tratamiento de dichas disoluciones. Asimismo, se ha llevado a cabo un estudio cinético del proceso de intercambio catiónico entre el indio(III y la resina Lewatit K-2621. Este estudio muestra que el proceso de intercambio responde a un mecanismo de difusión en la disolución o en la partícula de resina dependiendo de la concentración inicial del metal en el medio acuoso. El metal cargado en la resina puede ser eluido con disoluciones de ácido clorhídrico a 20 °C.

  10. Induction of DNA strand breaks in 14C-labelled cells

    International Nuclear Information System (INIS)

    Sundell-Bergman, S.; Johanson, K.J.

    1979-01-01

    Chinese hamster cells grown in vitro were labelled with 14 C-thymidine for 18 hours and after 3 hours in non-radioactive medium they were stored at 0 0 C for various periods ( 1 to 12 hours). During this treatment a number of DNA strand breaks were induced by 14 C decay which were not repaired at 0 0 C. The number of DNA strand breaks was determined using the DNA unwinding technique. At 0.5-1 dpm per cell a detectable number of DNA strand breaks were found. Treatment for six hours (1 dpm per cell) reduced the percentage of double-stranded DNA from 80 to 70%, corresponding to about 750 DNA strand breaks per cell. The rejoining of DNA strand breaks was studied after treatment for 12 hours at 0 0 C followed by incubation of the cells for various periods at 37 0 C. Most of the DNA strand breaks induced by 14 C decay at 0 0 C were repaired after incubation at 37 0 C for 15 minutes. Assuming an absorbed dose of 1.8 mGy per 14 C decay to the cell nucleus an RBE value close to 1 was found for internal irradiation from 14 C decay as compared with 60 Co-gamma irradiation. (author)

  11. 14C-labeling of isomeric perfluoroalkyl carboxanilide mixtures via electrofluorination

    International Nuclear Information System (INIS)

    Gajewski, R.P.; Terando, N.H.; Berard, D.F.

    1988-01-01

    Electrofluorination of benzoyl chloride-ring-UL- 14 C produced an isomer mixture of cyclic C 6 F 11 carbonyl fluorides, principally 1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane-ring-UL- 14 C carbonyl fluoride, which was derivatized with 2-bromo-4-nitroaniline and triethyl amine. The resultant carboxanilide mixture is designated as EL-499 labeled with 14 C in the perfluoro alkyl ring for use in metabolic studies. (author)

  12. Characterization of 14C in Swedish light water reactors.

    Science.gov (United States)

    Magnusson, Asa; Aronsson, Per-Olof; Lundgren, Klas; Stenström, Kristina

    2008-08-01

    This paper presents the results of a 4-y investigation of 14C in different waste streams of both boiling water reactors (BWRs) and pressurized water reactors (PWRs). Due to the potential impact of 14C on human health, minimizing waste and releases from the nuclear power industry is of considerable interest. The experimental data and conclusions may be implemented to select appropriate waste management strategies and practices at reactor units and disposal facilities. Organic and inorganic 14C in spent ion exchange resins, process water systems, ejector off-gas and replaced steam generator tubes were analyzed using a recently developed extraction method. Separate analysis of the chemical species is of importance in order to model and predict the fate of 14C within process systems as well as in dose calculations for disposal facilities. By combining the results of this investigation with newly calculated production rates, mass balance assessments were made of the 14C originating from production in the coolant. Of the 14C formed in the coolant of BWRs, 0.6-0.8% was found to be accumulated in the ion exchange resins (core-specific production rate in the coolant of a 2,500 MWth BWR calculated to be 580 GBq GW(e)(-1) y(-1)). The corresponding value for PWRs was 6-10% (production rate in a 2,775 MWth PWR calculated to be 350 GBq GW(e)(-1) y(-1)). The 14C released with liquid discharges was found to be insignificant, constituting less than 0.5% of the production in the coolant. The stack releases, routinely measured at the power plants, were found to correspond to 60-155% of the calculated coolant production, with large variations between the BWR units.

  13. Sensitive method for continuous air monitoring for /sup 14/C and /sup 3/H. Empfindliches verfahren zur koninuierlichen C-14 und H-3 luftueberwachung

    Energy Technology Data Exchange (ETDEWEB)

    Rudolph, J.; Weiss, W.

    1976-07-01

    In the monitoring of air for /sup 14/C and /sup 3/H the necessary sensitivity cannot be achieved by direct measurement, but only through continuous sampling and scintillation spectroscopy. The two radionuclides are separated from each other at the time of sampling. In addition, by a catalytic reaction over CuO at 600/sup 0/C, a differentiation is achieved between tritiated atmospheric water vapor (HTO), /sup 14/CO/sub 2/ and other isotopically labeled substances contained in the air. Tritium is obtained in the form of water and /sup 14/C as Na/sub 2//sup 14/CO/sub 3/. Radioactivity is measured in a scintillation spectrometer. For tritium this method has a detection limit of 0.8 pCi/m/sup 3/ or air, and for C/sup 14/ 0.6 pCi/m/sup 3/ of air. These values correspond to 15 to 30% of the mean background concentration for HTO and /sup 14/CO/sub 2/ observed up to the present.

  14. Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, A; Singh, M P; Singh, V K

    1982-05-01

    The nitrato-complexes, (Y(PyBzH)/sub 2/(NO/sub 3/)/sub 2/)NO/sub 3/.H/sub 2/O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole) are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm/sup -1/cm/sup 2/mol/sup -1/) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the positive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C/sub 2/v) and uncoordinated (D/sub 3/h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms.

  15. Nitrato-complexes of Y(III), La(III), Ce(III), Pr(III), Nd(III), Sm(III), Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl) benzimidazole

    International Nuclear Information System (INIS)

    Mishra, A.; Singh, M.P.; Singh, V.K.

    1982-01-01

    The nitrato-complexes, [Y(PyBzH) 2 (NO 3 ) 2 ]NO 3 .H 2 O and Nd, Sm, Gd, Tb, Dy, Ho ; n=1-3, m=0-0.5 ; PyBzh=2-(2 -pyridyl)benzimidazole] are formed on interaction of the ligand with metal nitrates in ethanol. The electrical conductance values (116-129 ohm -1 cm 2 mol -1 ) suggest 1:1 electrolyte-nature of the complexes. Magnetic moment values of Ce(2.53 B.M.), Pr(3.62 B.M.), Nd(3.52 B.M.), Sm(1.70 B.M.), Gd(8.06 B.M.), Tb(9.44 B.M.), Dy(10.56 B.M.) and Ho(10.51 B.M.) in the complexes confirm the terpositive state of the metals. Infrared evidences are obtained for the existance of both coordinated (C 2 v) and uncoordinated (D 3 h) nitrate groups. Electronic absorption spectra of Pr(III)-, Nd(III)-, Sm(III)-, Tb(III)-, Dy(III)- and Ho(III)-complexes have been analysed in the light of LSJ terms. (author)

  16. A fresnoite-structure-related mixed valent titanium(III/IV) chlorosilicate, Ba{sub 3}Ti{sub 2}Si{sub 4}O{sub 14}Cl: A flux crystal growth route to Ti(III) containing oxides

    Energy Technology Data Exchange (ETDEWEB)

    Abeysinghe, Dileka; Smith, Mark D.; Loye, Hans-Conrad zur, E-mail: zurloye@mailbox.sc.edu

    2017-06-15

    Single crystals of mixed valent barium titanium(III/IV) chlorosilicate, Ba{sub 3}Ti{sub 2}Si{sub 4}O{sub 14}Cl{sub 0.91}O{sub 0.09}, were grown in a high temperature molten chloride flux involving an in situ reduction step. The fresnoite structure related Ba{sub 3}Ti{sub 2}Si{sub 4}O{sub 14}Cl{sub 0.91}O{sub 0.09} crystallizes in the tetragonal space group P4/mbm with lattice parameters of a=8.6717(2) Å, c=18.6492(5) Å. The title compound exhibits a 3D structure consisting of 2D layers of fused Ti{sub 2}O{sub 9} and Si{sub 4}O{sub 12} groups and 2D layers of fused Ti{sub 2}O{sub 9}Cl{sub 2} and Si{sub 2}O{sub 7} groups that are linked via barium atoms. The in situ reduction of Ti(IV) to Ti(III) is achieved via the addition of metallic Mg to the flux to function as the reducing agent. The temperature dependence of the magnetic susceptibility shows simple paramagnetism above 100 K. There is a discontinuity in the susceptibility data below 100 K, which might be due to a structural change that takes place resulting in charge ordering. - Graphical abstract: The fresnoite structure related novel reduced barium titanium chlorosilicate, Ba{sub 3}Ti{sub 2}Si{sub 4}O{sub 14}Cl{sub 0.91}O{sub 0.09}, were synthesized via flux method. An in situ reduction of Ti(IV) to Ti(III) achieved using Mg metal. The 3D structure consists 2D layers of fused Ti{sub 2}O{sub 9} and Si{sub 4}O{sub 12} and 2D layers of fused Ti{sub 2}O{sub 9}Cl{sub 2} and Si{sub 2}O{sub 7} connected via barium atoms. Compound shows simple paramagnetism above 100 K. - Highlights: • The fresnoite related Ba{sub 3}Ti{sub 2}Si{sub 4}O{sub 14}Cl{sub 0.91}O{sub 0.09} were grown via molten flux method. • The in situ reduction of Ti(IV) to Ti(III) is achieved using metallic Mg. • 2D layers of Ti{sub 2}O{sub 9} and Si{sub 4}O{sub 12} and Ti{sub 2}O{sub 9}Cl{sub 2} and Si{sub 2}O{sub 7} connect via Ba atoms. • The magnetic susceptibility shows simple paramagnetism above 100 K.

  17. Modified synthesis of 11-[14C]-clozapine

    International Nuclear Information System (INIS)

    Matloubi, Hojatollah; Ghandi, Mehdi; Zarrindast, M.-R.; Saemian, Nader

    2001-01-01

    The reported synthetic pathway of 8-chloro-11-(4-methyl-1-piperazinyl)-11-[ 14 C]-5H-dibenzo[b,e][1,4]diazapine (clozapine) was modified in several steps. The synthetic pathway was shortened by 60% and the total yield was increased from 6% to 23%

  18. Absorption, Translocation and Metabolism of {sup 14}C-Labelled Dichlobenil

    Energy Technology Data Exchange (ETDEWEB)

    Pate, D. A.; Funderburk, Jr., H. H. [Auburn University Agricultural Experiment Station, Auburn, AL (United States)

    1966-05-15

    Autoradiographs of bean (Phaseolus vulgaris L.) and alligatorweed (Alternanthera philoxeroides (Mart.) Griseb.) indicated that {sup 14}C-nitrile-labelled dichlobenil (2,6-dichlorobenzonitrile) was slightly absorbed by the leaf and some translocation occurred following foliar application. Plants with roots submersed in radioactive aqueous solution absorbed and translocated the {sup 14}C throughout the plant. An investigation of some of the chemical and physical properties of {sup 14}C-nitrile-labelled dichlobenil was conducted. Loss because of volatilization from counting planchets was considerably reduced by application of acrylic plastic immediately after the solution dried. The plastic coating also eliminated contamination of counting chambers and windows. Two higher plants (bean and alligatorweed ) and four fungi (Fusarium sp., Geotrichum sp., Penicillium sp., Trichoderma sp.) were selected for metabolism studies. Dichlobenil- {sup 14}C was added to Hoagland and Arnon's nutrient solution containing beans or alligatorweed and to liquid cultures containing the other organisms for 12 to 120 h. Extracts from the plants or fungi were chromatographed on silica gel thin-layers. Autoradiographs of the thin-layer chromatographed aqueous extracts revealed a {sup C}-labelled compound of Rf 0.25 that differed from that of dichlobenil, which was 0.6. After esterification of the extracts, a {sup 14}C-labelled compound was observed at Rf 0.95 on thin-layer chromatograms. Chromatography of the unaltered extracts with 2,6- dichlorobenzoic acid revealed identical Rf-values. The esterified aqueous extracts chromatographed precisely with methyl-2,6-dichlorobenzoate. Gas chromatography of the {sup 14}C-labelled compound with an Rf of 0.95 exhibited a retention time identical to that of methyl-2,6-dichlorobenzoate. The quantity of {sup 14}C-labelled compound that chromatographed as 2,6-dichlorobenzoate increased with time of exposure of the various test organisms to dichlobenil {sup

  19. Studies on bound residues of 14C-malathion in soil

    International Nuclear Information System (INIS)

    Hussain, A.; Azam, F.; Malik, K.A.

    1984-01-01

    The extractability and formation of bound 14 C-labelled residues in clay loam soil under laboratory conditions were investigated with malathion. 14 C-malathion rapidly decomposed to 14 CO 2 . Twelve days after treatment 56% of the applied dose was lost as 14 CO 2 . Methanol gave the highest extraction efficiency; 6% of the applied radiocarbon was extractable while bound residues amounted to 38%. The soil containing 14 C-labelled residues was fractionated into humic acid, fulvic acid and humin fractions. These fractions contained 7.83%, 16.81% and 19.36%, respectively of applied radiocarbon. (author)

  20. Percutaneous absorption of [14C]DDT and [14C]benzo[a]pyrene from soil

    International Nuclear Information System (INIS)

    Wester, R.C.; Maibach, H.I.; Bucks, D.A.; Sedik, L.; Melendres, J.; Liao, C.; DiZio, S.

    1990-01-01

    The objective was to determine percutaneous absorption of DDT and benzo[a]pyrene in vitro and in vivo from soil into and through skin. Soil (Yolo County 65-California-57-8; 26% sand, 26% clay, 48% silt) was passed through 10-, 20-, and 48-mesh sieves. Soil then retained by 80-mesh was mixed with [14C]-labeled chemical at 10 ppm. Acetone solutions at 10 ppm were prepared for comparative analysis. Human cadaver skin was dermatomed to 500 microns and used in glass diffusion cells with human plasma as the receptor fluid (3 ml/hr flow rate) for a 24-hr skin application time. With acetone vehicle, DDT (18.1 +/- 13.4%) readily penetrated into human skin. Significantly less DDT (1.0 +/- 0.7%) penetrated into human skin from soil. DDT would not partition from human skin into human plasma in the receptor phase (less than 0.1%). With acetone vehicle, benzo[a]pyrene (23.7 +/- 9.7%) readily penetrated into human skin. Significantly less benzo[a]pyrene (1.4 +/- 0.9%) penetrated into human skin from soil. Benzo[a]pyrene would not partition from human skin into human plasma in the receptor phase (less than 0.1%). Substantivity (skin retention) was investigated by applying 14C-labeled chemical to human skin in vitro for only 25 min. After soap and water wash, 16.7 +/- 13.2% of DDT applied in acetone remained absorbed to skin. With soil only 0.25 +/- 0.11% of DDT remained absorbed to skin. After soap and water wash 5.1 +/- 2.1% of benzo[a]pyrene applied in acetone remained absorbed to skin. With soil only 0.14 +/- 0.13% of benzo[a]pyrene remained absorbed to skin

  1. Evaluation of 14C abundance in soil respiration using accelerator mass spectrometry

    International Nuclear Information System (INIS)

    Koarashi, Jun; Iida, Takao; Moriizumi, Jun; Asano, Tomohiro

    2004-01-01

    To clarify the behavior of 14 C in terrestrial ecosystems, 14 C abundance in soil respiration was evaluated in an urban forest with a new method involving a closed chamber technique and 14 C measurement by accelerator mass spectrometry (AMS). Soil respiration had a higher Δ 14 C than the contemporary atmosphere. This indicates that a significant portion of soil respiration is derived from the decomposition of soil organic matter enriched in 14 C by atmospheric nuclear weapons tests, with a notable time lag between atmospheric 14 C addition and re-emission from soil. On the other hand, δ 14 C in soil respiration demonstrated that 14 C abundance ratio itself in soil-respired CO 2 is not always high compared with that in atmospheric CO 2 because of the isotope fractionation during plant photosynthesis and microbial decomposition of soil organic matter. The Δ 14 C in soil respiration was slightly lower in August than in March, suggesting a relatively high contribution of plant root respiration and decomposition of newly accumulated and/or 14 C-depleted soil organic matter to the total soil respiration in August

  2. Uptake of [2-14C]abscisic acid and distribution of 14C in apple embryos

    International Nuclear Information System (INIS)

    Barthe, P.; Bulard, C.

    1981-01-01

    Pyrus malus L. var. Golden delicious embryos were incubated with (+-)-[2- 14 C] abscisic acid (ABA). After incubations of various durations, the radioactivity was measured in whole embryos, cotyledons, and embryonic axes. With either 48-h or 16-d incubation periods, the uptake of [ 14 C] ABA depended upon the mode of culture used. The lowest values corresponded to the absorption by the embryonic axis, the highest to the absorption by the distal parts of the two cotyledons. The cotyledons accumulated the main part of the radioactivity under all conditions. Dormant and almost completely after-ripened embryos cultivated for 4 d showed no significant differences in the radioactivity uptake for identical modes of culture. There was a linear relationship between exogenous ABA concentrations (0.5 to 3.10 -5 M) and ABA uptake for embryos cultivated for 4 d with the distal parts of the cotyledons immersed in the medium. (orig.) [de

  3. Synthesis of [diene-"1"4C] curcumin at high specific activity

    International Nuclear Information System (INIS)

    Filer, Crist N.; Lacy, James M.; Wright, Christopher

    2016-01-01

    An efficient method is described to label curcumin with "1"4C at high specific activity. - Highlights: • This paper describes the synthesis of ["1"4C] Curcumin at the highest specific activity and total activity amount yet reported. • The "1"4C label was installed in the diene framework of Curcumin. • This paper also describes the characterization of ["1"4C] Curcumin by HPLC and mass spectrometry.

  4. (4-Chloroacetanilido-κ2N,Obis[2-(pyridin-2-ylphenyl-κ2C1,N]iridium(III

    Directory of Open Access Journals (Sweden)

    Lijun Sun

    2013-02-01

    Full Text Available In the neutral mononuclear iridium(III title compound, [Ir(C8H7ClNO(C11H8N2], the IrIII atom adopts an octahedral geometry, and is coordinated by two 2-phenylpyridyl ligands and one anionic 4-chloroacetanilide ligand. The 2-phenylpyridyl ligands are arranged in a cis-C,C′ and cis-N,N′ fashion. Each 2-phenylpyridyl ligand forms a five-membered ring with the IrIII atom. The 2-phenylpyridyl planes are perpendicular to each other [dihedral angle = 89.9 (1°]. The Ir—C and Ir—N bond lengths are comparable to those reported for related iridium(III 2-phenylpyridyl complexes. The remaining two coordination sites are occupied by the amidate N and O atoms, which form a four-membered ring with the iridium atom (Ir—N—C—O. The amidate plane is nearly perpendicular to both 2-phenylpyridyl ligands [dihedral angles = 87.8 (2 and 88.3 (2°].

  5. Effective modern C++ 42 specific ways to improve your use of C++11 and C++14

    CERN Document Server

    Meyers, Scott

    2015-01-01

    At first glance, C++11 and C++14 are defined by the new features they introduce, e.g., auto type declarations, move semantics, lambda expressions, and concurrency support. Information on these features is easy to come by, but learning to apply them effectively (such that the resulting software is correct, efficient, maintainable, and portable) is more challenging. That’s the role of this book. It describes how to write effective software using C++11 and C++14, i.e., using modern C++. Topics include: * The pros and cons of uniform initialization, noexcept specifications, perfect forwarding, and smart pointer make functions. * The relationships among std::move, std::forward, rvalues references, and universal references. * The most effective forms of lambda capture. * How best practices in “old” C++ programming (i.e., C++98) require revision for modern C++. Effective Modern C++ follows the proven format of Scott Meyers’ earlier Effective books (Effective C++, More Effective C++, and Effective STL), but c...

  6. Low-level (submicromole) environmental 14C metrology

    International Nuclear Information System (INIS)

    Currie, L.A.; Kessler, J.D.; Marolf, J.V.; McNichol, A.P.; Stuart, D.R.; Donoghue, J.C.; Donahue, D.J.; Burr, G.S.; Biddulph, D.

    2000-01-01

    Accelerator mass spectrometry (AMS) measurements of environmental 14 C have been employed during the past decade at the several micromole level (tens of μg carbon), but advanced research in the atmospheric and marine sciences demands still higher (μg) sensitivity, an extreme example being the determination of 14 C in elemental or 'black' carbon (BC) at levels of 2-10 μg per kg of Greenland snow and ice (Currie et al., 1998). A fundamental limitation for 14 C AMS is Poisson counting statistics, which sets in at about 1 μg modern-C. Using the small sample (25 μg) AMS target preparation facility at NOSAMS (Pearson et al., 1998), and the microsample combustion-dilution facility at NIST, we have demonstrated an intrinsic modern-C quantification limit (m Q ) of ca. 0.9 μg, based on a 1-parameter fit to the empirical AMS variance function. (For environmental 14 C, the modern carbon quantification limit is defined as that mass (m Q ) corresponding to 10% relative standard deviation (rsd) for the fraction of modern carbon, σ(f M )/f M .) Stringent control, required for quantitative dilution factors (DL), is achieved with the NIST on-line manometric/mass spectrometry facility that compensates also for unsuspected trace impurities from vigorous chemical processing (e.g., acid digestion). Our current combustion blank is trivial (mean: 0.16 ± 0.02 μg C, n=13) but lognormally distributed (dispersion [σ]: 0.07 ± 0.01 μg). An iterative numerical expression is introduced to assess the quantitative impacts of fossil and modern carbon blank components on m Q ; and a new 'clean chemistry' BC processing system is described for the minimization of such blanks. For the assay of soot carbon in Greenland snow/ice, the overall processing blank has been reduced from nearly 7 μg total carbon to less than 1 μg, and is undetectable for BC

  7. Thermodynamic model for solution behavior and solid-liquid equilibrium in Na-Al(III)-Fe(III)-Cr(III)-Cl-H2O system at 25°C

    Science.gov (United States)

    André, Laurent; Christov, Christomir; Lassin, Arnault; Azaroual, Mohamed

    2018-03-01

    The knowledge of the thermodynamic behavior of multicomponent aqueous electrolyte systems is of main interest in geo-, and environmental-sciences. The main objective of this study is the development of a high accuracy thermodynamic model for solution behavior, and highly soluble M(III)Cl3(s) (M= Al, Fe, Cr) minerals solubility in Na-Al(III)-Cr(III)-Fe(III)-Cl-H2O system at 25°C. Comprehensive thermodynamic models that accurately predict aluminium, chromium and iron aqueous chemistry and M(III) mineral solubilities as a function of pH, solution composition and concentration are critical for understanding many important geochemical and environmental processes involving these metals (e.g., mineral dissolution/alteration, rock formation, changes in rock permeability and fluid flow, soil formation, mass transport, toxic M(III) remediation). Such a model would also have many industrial applications (e.g., aluminium, chromium and iron production, and their corrosion, solve scaling problems in geothermal energy and oil production). Comparisons of solubility and activity calculations with the experimental data in binary and ternary systems indicate that model predictions are within the uncertainty of the data. Limitations of the model due to data insufficiencies are discussed. The solubility modeling approach, implemented to the Pitzer specific interaction equations is employed. The resulting parameterization was developed for the geochemical Pitzer formalism based PHREEQC database.

  8. Metabolism of U14C palmitic and 1-14C caproic acids by lettuce seeds during early germination

    International Nuclear Information System (INIS)

    Salon, C.; Raymond, P.; Pradet, A.

    1986-01-01

    Germinating lettuce embryos (before radicule emergence) were fed with either U 14 C palmitic acid or 1 14 C caproic acid until a metabolic steady state was reached. The bulk of labelled caproate was evolved as respiratory CO 2 (52%) and incorporated into organic and amino acids (38%) and only a small part incorporated into lipids whereas most of labelled palmitic acid was found into lipids (92%) and only 8% evolved as CO 2 and incorporated into organic and amino acids. The label distribution at steady state in intermediates linked to the T.C.A. cycle was interpreted using a metabolic model. They found that the two fatty acids were degraded by β-oxidation and incorporated into the T.C.A. cycle as acetylCoA suggesting that β-oxidation is located in the mitochondria. The results also indicate that lipids contribute for at least 90% to the carbon supply to respiration

  9. Forensic applications of {sup 14}C bomb-pulse dating

    Energy Technology Data Exchange (ETDEWEB)

    Zoppi, U. E-mail: ugo@ansto.gov.au; Skopec, Z.; Skopec, J.; Jones, G.; Fink, D.; Hua, Q.; Jacobsen, G.; Tuniz, C.; Williams, A

    2004-08-01

    After a brief review of the basics of {sup 14}C bomb-pulse dating, this paper presents two unique forensic applications. Particular attention is dedicated to the use of the {sup 14}C bomb-pulse to establish the time of harvest of illicit drugs such as heroin and opium. Preliminary measurements of {sup 14}C concentrations in milligram samples taken from seized drugs are presented. {sup 14}C bomb-pulse dating can determine whether drug distribution originates from stockpiles or recent manufacture, and support the action of law enforcement authorities against criminal organisations involved in drug trafficking. In addition, we describe the dating of wine vintages for a number of authenticated single label vintage red wines from the Barossa Valley - South Australia. Our results show that radiocarbon dating can be used to accurately determine wine vintages and therefore reveal the addition of unrelated materials of natural and synthetic origin.

  10. Apolipoproteins A-I, B, and C-III and Obesity in Young Adult Cherokee

    Directory of Open Access Journals (Sweden)

    Wenyu Wang

    2017-01-01

    Full Text Available Since young adult Cherokee are at increased risk for both diabetes and cardiovascular disease, we assessed association of apolipoproteins (A-I, B, and C-III in non-HDL and HDL with obesity and related risk factors. Obese participants (BMI ≥ 30 aged 20–40 years (n=476 were studied. Metabolically healthy obese (MHO individuals were defined as not having any of four components of the ATP-III metabolic syndrome after exclusion of waist circumference, and obese participants not being MHO were defined as metabolically abnormal obese (MAO. Associations were evaluated by correlation and regression modeling. Obesity measures, blood pressure, insulin resistance, lipids, and apolipoproteins were significantly different between groups except for total cholesterol, LDL-C, and HDL-apoC-III. Apolipoproteins were not correlated with obesity measures with the exception of apoA-I with waist and the waist : height ratio. In a logistic regression model apoA-I and the apoB : apoA-I ratio were significantly selected for identifying those being MHO, and the result (C-statistic = 0.902 indicated that apoA-I and the apoB : apoA-I ratio can be used to identify a subgroup of obese individuals with a significantly less atherogenic lipid and apolipoprotein profile, particularly in obese Cherokee men in whom MHO is more likely.

  11. Study of the C-14-contamination potential of C-impurities in CuO and Fe

    NARCIS (Netherlands)

    Vandeputte, K; Moens, L; Dams, R; van der Plicht, Johannes

    1998-01-01

    The carbon concentration in CuO and iron was determined by isolating C. The values were in agreement with results reported in other studies. Contaminating carbon from CuO and Fe was transformed to AMS targets and measured for C-14. C-traces in CuO were shown to be the major contribution to the C-14

  12. 14C and 13C in the atmosphere and soil air at two localities of Slovakia

    International Nuclear Information System (INIS)

    Sivo, A.; Simon, J.; Richtarikova, M.; Holy, K.; Polaskova, A.; Bulko, M.; Hola, O.

    2006-01-01

    In this paper there are presented the long-term measurements of 13 R and 14 R in urban and countryside atmosphere. The different conditions and particularities of both the localities which influence on the mentioned characteristics are pointed out. The existence of δ 13 C and δ 14 C variations and their phase correlation were confirmed as well as their origin were qualitatively explained. By means of the non-linear regression and harmonic analysis the trends of δ 13 C and δ 14 C variations was found. The study of δ 13 C and δ 14 C courses has shown that it can be used as an effective tool to determine the level of the anthropogenic CO 2 pollution of the atmosphere. (authors)

  13. Physical Research Laboratory radiocarbon 14C dates : CS-I

    International Nuclear Information System (INIS)

    Agrawal, D.P.; Krishnamurthy, R.V.; Kusumgar, Sheela; Pant, R.K.

    1978-01-01

    The 14 C dates of archaeological samples measured at the Radiocarbon Laboratory of the Physical Research Laboratory, Ahmedabad are presented. Samples were converted into methane and measured in gas proportional counters. Ninety-five percent activity of NBS oxalic acid was used as modern standard. The dates in years B.P. are given for each sample based on the half-life values of 5568 +- 30 years and 5730 +- 40 years, the latter within parenthesis. The dates are not calibrated for 14 C/ 12 C variations. To convert the dates into AD/BC scale, 1950 AD should be used as reference year. A number of 14 C dates (PRL-81, -83, -67, -68) now confirm that the Painted Grey Ware culture extended upto the 3rd century BC. Some of the dates from Barkhera (PRL-113), Bateshwar (PRL-200), Bhimbetka (PRL-17) and Koldihawa (PRL-100, 101) are older than normally expected, probably indicative of some hitherto unknown basal cultures in these regions. 14 C dates on in situ Megalithic materials do not seem to go beyond 200 BC. (author)

  14. Determination of the NPP Krsko reactor core safety limits using the COBRA-III-C code

    International Nuclear Information System (INIS)

    Lajtman, S.; Feretic, D.; Debrecin, N.

    1989-01-01

    This paper presents the NPP Krsko reactor core safety limits determined by the COBRA-III-C code, along with the methodology used. The reactor core safety limits determination is a part of reactor protection limits procedure. The results obtained were compared to safety limits presented in NPP Krsko FSAR. The COBRA-III-C NPP Krsko design core steady state thermal hydraulics calculation, used as the basis for the safety limits calculation, is presented as well. (author)

  15. Systemic translocation and metabolism of 14C-metalaxyl in citrus

    International Nuclear Information System (INIS)

    Musumeci, M.R.; Ruegg, E.F.

    1984-01-01

    Systemic uptake and translocation of 14 C-metalaxyl to citrus seedlings from soils (Humic Gley and Yellow Red Latosol) with different physical - chemical properties are studied. Seedlings of Citrus limonia are treated with 14 C-metalaxyl. (M.A.C.) [pt

  16. Charged particle reaction studies on /sup 14/C. [Spectroscopic factors

    Energy Technology Data Exchange (ETDEWEB)

    Cecil, F E; Shepard, J R; Anderson, R E; Peterson, R J; Kaczkowski, P [Colorado Univ., Boulder (USA). Nuclear Physics Lab.

    1975-12-22

    The reactions /sup 14/C(p,d), (d,d') and (d,p) have been measured for E/sub p/ = 27 MeV and E/sub d/ = 17 MeV. The (d,d') and (d,p) reactions were studied between theta/sub lab/ = 15/sup 0/ and 85/sup 0/; the (p,d) reactions, between theta/sub lab/ = 5/sup 0/ and 40/sup 0/. The /sup 14/C deformation parameters were deduced from the deuteron inelastic scattering and found to agree with deformations measured in nearby doubly even nuclei. The spectroscopic factors deduced from the (p,d) reaction allowed a /sup 14/C ground-state wave function to be deduced which compares favorably with a theoretically deduced wave function. The (p,d) and (d,p) spectroscopic factors are consistent. The implications of our /sup 14/C ground-state wave function regarding the problem of the /sup 14/C hindered beta decay are discussed.

  17. 14C-labeled diesel exhaust particles: chemical characteristics and bioavailability studies

    International Nuclear Information System (INIS)

    Sun, J.D.; Wolff, R.K.; Dutcher, J.S.; Brooks, A.L.

    1981-01-01

    Little is known about the deposition, retention and biological fate of the organic compounds associated with diesel exhaust particles. In the studies reported here, a one-cylinder diesel engine was operated on diesel fuel spiked with 14 C-benzene, 14 C-hexadecane or 14 C-dotriacontane to generate 14 C-labeled diesel exhaust. Approximately 1% of the exhaust radioactivity was associated with the particulate phase of diesel exhaust. Chemical fractionation of the particle extract showed the 14 C to be present in each of the various chemical class fractions collected. Serum removed approx. 60% of the dichloromethane extractable radioactivity from these diesel particles while saline removed only approx. 6%. This suggested that the organic compounds may be removed from diesel particles in vivo. Future inhalation exposures of rodents to 14 C-labeled diesel exhausts are planned to gain additional information on the health risk of human exposure to diesel exhaust

  18. Isothiocyanato complexes of Gd(III), Tb(III), Dy(III) and Ho(III) with 2-(2'-pyridyl)benzimidazole

    Energy Technology Data Exchange (ETDEWEB)

    Mishra, A; Singh, V K

    1982-01-01

    Six-coordinated complexes of the type (Ln(PyBzH)/sub 2/NCS.H/sub 2/O) (NCS)/sub 2/.nH/sub 2/O/mC/sub 2/H/sub 5/OH (Ln = Gd(III), Tb(III), Dy(III) and Ho(III), n=1-2; m=1) have been prepared from Ln(NCS)/sub 6//sup 3 -/. The room temperature magnetic moment values confirm the terpositive state of the lanthanide ions. Infrared spectra suggest the N-coordination of thiocyanate group. Electronic spectral studies of Tb(III), Dy(III) and Ho(III) complexes have been made in terms of LSJ term energies. 13 refs.

  19. Fate of [14C]arsanilic acid in pigs and chickens

    International Nuclear Information System (INIS)

    Aschbacher, P.W.; Feil, V.J.

    1991-01-01

    Arsanilic acid uniformly labeled with 14 C in the benzene ring was used to determine the metabolic fate of oral arsanilic acid in pigs and chickens. Arsanilic acid was well absorbed in both species, and urine was the predominant route of excretion. The bile was a minor ( 14 C, respectively). Only 25% of the 14 C in pig feces was extractable, and no metabolites could be isolated. Arsanilic acid was the only radioactive compound isolated from urine of colostomized roosters, and there was no suggestion of other metabolites from the isolation scheme employed. No attempt was made to isolate 14 C compounds in feces from colostomized roosters or in excreta from normal roosters

  20. Determination of gluconeogenesis in vivo with 14C-labeled substrates

    International Nuclear Information System (INIS)

    Katz, J.

    1985-01-01

    A mitochondrial model of gluconeogenesis and the tricarboxylic acid cycle, where pyruvate is metabolized via pyruvate carboxylase and pyruvate dehydrogenase, and pyruvate kinase is examined. The effect of the rate of tricarboxylic acid flux and the rates of the three reactions of pyruvate metabolism on the labeling patterns from [ 14 C]pyruvate and [ 14 C]acetate are analyzed. Expressions describing the specific radioactivities and 14 C distribution in glucose as a function of these rates are derived. Specific radioactivities and isotopic patterns depend markedly on the ratio of the rates of pyruvate carboxylation and decarboxylation to the rate of citrate synthesis, but the effect of phosphoenolpyruvate hydrolysis is minor. The effects of these rates on 1) specific radioactivity of phosphoenolpyruvate, 2) labeling pattern in glucose, and 3) contribution of pyruvate, acetyl-coenzyme A, and CO 2 to glucose carbon are illustrated. To determine the contribution of lactate or alanine to gluconeogenesis, experiments with two compounds labeled in different carbons are required. Methods in current use to correct for the dilution of 14 C in gluconeogenesis from [ 14 C]pyruvate are shown to be erroneous. The experimental design and techniques to determine gluconeogenesis from 14 C-labeled precursors are presented and illustrated with numerical examples

  1. A study of the reactions 14C( vector d, dprime)14C and 14C ( vector d, p)15C at 16.0 MeV

    International Nuclear Information System (INIS)

    Murillo, G.; Sen, S.; Darden, S.E.

    1994-01-01

    Cross-section and vector-analyzing-power measurements for 14 C(d, d prime) and 14 C(d, p) reactions have been carried out for E d =16 MeV. The inelastic-scattering data have been analyzed using the DWBA with a collective and a microscopic model form-factor and also by using the coupled-channels formalism with a vibrational model form-factor. It is observed that while the cross-section angular-distribution data for the two 2 + states at E x =7.012 and 8.318 MeV are very similar, the corresponding vector analyzing powers are quite different. The results of the analyses indicate that the distinctive characteristics probably arise from the difference in the relative importance of the proton and neutron components in the transition amplitude. The 3 - state at E x =6.728 MeV is identified as predominantly a 1p-3h state. Although the deformation parameters are relatively large, the single-particle structure aspects play a more dominant role than channel-coupling effects in populating the inelastic states. The transfer reaction data have been analyzed using the DWBA for bound and unbound states. The importance of two-step processes has been investigated via coupled-reaction-channels calculations. The g.s. and the states with excitation energies 0.770, 3.103 and 4.78 MeV in 15 C are populated primarily by a one-step process with a small two-step contribution in the case of the 3.103 MeV state. The 4.22 MeV state is populated predominantly by two-step processes. The 4.78 and the 5.83 MeV states have been identified as 1p-2h and 3p-4h, [3]/[2] + state, respectively, in an earlier report. There is close similarity in the level structures and reaction mechanisms between the states of 15 C and 17 O populated via the (d, p) reaction. ((orig.))

  2. The synthesis of [U-14C phenyl] LS 840606, an agricultural fungicide

    International Nuclear Information System (INIS)

    Madegard, G.; Mestre, P.; Raimond, P.; Noel, J.-P.

    1995-01-01

    2,2',4'-Trichloro-[ring U- 14 C]acetophenone was the key intermediate of this synthesis patterned after the industrial route. An unexpected poor yield was observed during the preparation by the Friedel-Crafts reaction of chloroacetyl chloride with 1,3-dichloro-[U- 14 C]benzene, possibly the result of an isotope effect although this poor yield might be explained by other factors. Two routes were checked for the preparation of 1,3-dichloro-[U- 14 C]benzene. The action of CCl 4 with 1,3-dinitro-[U- 14 C]benzene at 280 o C was entailed with explosions. A safer route started from [U- 14 C]aniline via 2,4-dichloro-[ring U- 14 C]acetanilide. Friedel-Crafts reaction with acetyl chloride gave rise in 52% yield to 2',4'-dichloro-[ring U- 14 C]acetophenone which was brominated to 2-bromo-2',4'-dichloro-[ring U- 14 C]acetophenone; was condensed with 2,2-ethylenedioxy)etylmagnesium bromide to compound, was condensed with 1,2,4-triazole then successively treated with HCl:water:dioxane and 2,2,2-trifluoroethanol/HCl. Separation of the two diastereomers by medium pressure liquid chromatography. 7% overall radioactivity yield from [U- 14 C]aniline. Radiochemical purity 99%. (author)

  3. Dissipation and leaching of 14C-monocrotophos in soil columns

    International Nuclear Information System (INIS)

    Vig, K.; Singh, D.K.; Agarwal, H.C.

    2001-01-01

    Dissipation and leaching of 14 C-monocrotophos was studied in the field. Two sets of PVC cylinders were used - one set received only 14 C monocrotophos and the other received 14 C-monocrotophos along with dimethoate, deltamethrin, endosulfan, cypermethrin and 1.06 mg unlabelled monocrotophos. Both setups showed a similar pattern of dissipation with a half-life of 277.2 days. Leaching of monocrotophos was observed into the 30cm soil layer. (author)

  4. The removal of toxic metals from liquid effluents by ion exchange resins. Part IV: Chromium(III)/H+ /Lewatit SP112; La eliminación de metales tóxicos presentes en efluentes líquidos mediante resinas de cambio iónico. Parte IV: cromo(III)/H+/Lewatit SP112

    Energy Technology Data Exchange (ETDEWEB)

    Alguacil, F.J.

    2017-09-01

    This investigation presented results on the removal of chromium(III), from aqueous solution in the 0-5 pH range, using Lewatit SP112 cationic exchange resin. Several aspects affecting the ion exchange process were evaluated, including: the influence of the stirring speed, temperature, pH of the solution, resin dosage and aqueous ionic strength. The selectivity of the system was tested against the presence of other metals in the aqueous solution, whereas the removal of chromium(III) from solutions was compared with results obtained using multiwalled carbon nanotubes as adsorbents. From the batch experimental data, best fit of the results is obtained with the Langmuir model, whereas the ion exchange process is best explained by the pseudo-second order model, moreover, experimental data responded well to the film-diffusion controlled model. Elution of the chromium(III) loaded into the resin is well accomplished by the use of sodium hydroxide solutions. [Spanish] En este trabajo se presentan los resultados obtenidos en la eliminación de cromo(III) de disoluciones acuosas (pH 0-5) mediante la resina de intercambio catiónico Lewatit SP112. Se han investigado algunas variables que pueden afectar al sistema: influencia de la agitación, temperatura, pH y fuerza iónica del medio acuoso y cantidad de resina; también se ha investigado acerca de la selectividad del sistema cuando otros metales están presentes en el medio acuoso, comparándose los resultados de la eliminación del cromo(III) usando la resina con los resultados obtenidos cuando se emplea otro adsorbente como son los nanotubos de carbono de pared múltiple. Los resultados experimentales indican que la carga del cromo(III) en la resina responde mejor al modelo de Langmuir, mientras que los modelos cinéticos indican que la carga del metal en la resina responde al modelo de pseudo-segundo orden y difusión en la capa límite. La elución del cromo(III) se realiza con disoluciones de hidróxid.

  5. Capture reactions on C-14 in nonstandard big bang nucleosynthesis

    Science.gov (United States)

    Wiescher, Michael; Gorres, Joachim; Thielemann, Friedrich-Karl

    1990-01-01

    Nonstandard big bang nucleosynthesis leads to the production of C-14. The further reaction path depends on the depletion of C-14 by either photon, alpha, or neutron capture reactions. The nucleus C-14 is of particular importance in these scenarios because it forms a bottleneck for the production of heavier nuclei A greater than 14. The reaction rates of all three capture reactions at big bang conditions are discussed, and it is shown that the resulting reaction path, leading to the production of heavier elements, is dominated by the (p, gamma) and (n, gamma) rates, contrary to earlier suggestions.

  6. Connective tissue-activating peptide III (CTAP-III): cloning the synthetic gene and characterization of the protein expressed in E. coli

    International Nuclear Information System (INIS)

    Johnson, P.H.; Castor, C.W.; Walz, D.A.

    1986-01-01

    CTAP-III, an α-granule protein secreted by human platelets, is known to stimulate mitogenesis, extracellular matrix synthesis, and plasminogen activator synthesis in human fibroblast cultures. From its primary sequence, a synthetic gene was constructed to code for a methionine-free derivative (Leu substituted for Met-21), then cloned and expressed in E. coli using a new expression vector containing regulatory elements of the colicin E1 operon. Partially purified recombinant CTAP-III showed a line of identity with CTAP-III by immunodiffusion against rabbit antibody to platelet-derived CTAP-III. Immunodetection of the reduced protein after SDS-PAGE electrophoresis showed a molecular weight (mobility) in agreement with the natural form. Biologic activity of rCTAP-III eluted from an antiCTAP-III immunoaffinity column was measured in human synovial cell bioassay systems. rCTAP-III stimulated synovial cell synthesis of 14 C-hyaluronic acid approximately 13-fold; significant (P < 0.001) mitogenesis was also observed. These studies indicate that a sufficient quantity of bioactive peptide can be obtained for a more comprehensive study of its biologic properties

  7. Heterologous gene expression and functional analysis of a type III polyketide synthase from Aspergillus niger NRRL 328

    Energy Technology Data Exchange (ETDEWEB)

    Kirimura, Kohtaro, E-mail: kkohtaro@waseda.jp; Watanabe, Shotaro; Kobayashi, Keiichi

    2016-05-13

    Type III polyketide synthases (PKSs) catalyze the formation of pyrone- and resorcinol-types aromatic polyketides. The genomic analysis of the filamentous fungus Aspergillus niger NRRL 328 revealed that this strain has a putative gene (chr-8-2: 2978617–2979847) encoding a type III PKS, although its functions are unknown. In this study, for functional analysis of this putative type III PKS designated as An-CsyA, cloning and heterologous expression of the An-CsyA gene (An-csyA) in Escherichia coli were performed. Recombinant His-tagged An-CsyA was successfully expressed in E. coli BL21 (DE3), purified by Ni{sup 2+}-affinity chromatography, and used for in vitro assay. Tests on the substrate specificity of the His-tagged An-CsyA with myriad acyl-CoAs as starter substrates and malonyl-CoA as extender substrate showed that His-tagged An-CsyA accepted fatty acyl-CoAs (C2-C14) and produced triketide pyrones (C2-C14), tetraketide pyrones (C2-C10), and pentaketide resorcinols (C10-C14). Furthermore, acetoacetyl-CoA, malonyl-CoA, isobutyryl-CoA, and benzoyl-CoA were also accepted as starter substrates, and both of triketide pyrones and tetraketide pyrones were produced. It is noteworthy that the His-tagged An-CsyA produced polyketides from malonyl-CoA as starter and extender substrates and produced tetraketide pyrones from short-chain fatty acyl-CoAs as starter substrates. Therefore, this is the first report showing the functional properties of An-CsyA different from those of other fungal type III PKSs. -- Highlights: •Type III PKS from Aspergillus niger NRRL 328, An-CsyA, was cloned and characterized. •An-CsyA produced triketide pyrones, tetraketide pyrones and pentaketide resorcinols. •Functional properties of An-CsyA differs from those of other fungal type III PKSs.

  8. Heterologous gene expression and functional analysis of a type III polyketide synthase from Aspergillus niger NRRL 328

    International Nuclear Information System (INIS)

    Kirimura, Kohtaro; Watanabe, Shotaro; Kobayashi, Keiichi

    2016-01-01

    Type III polyketide synthases (PKSs) catalyze the formation of pyrone- and resorcinol-types aromatic polyketides. The genomic analysis of the filamentous fungus Aspergillus niger NRRL 328 revealed that this strain has a putative gene (chr-8-2: 2978617–2979847) encoding a type III PKS, although its functions are unknown. In this study, for functional analysis of this putative type III PKS designated as An-CsyA, cloning and heterologous expression of the An-CsyA gene (An-csyA) in Escherichia coli were performed. Recombinant His-tagged An-CsyA was successfully expressed in E. coli BL21 (DE3), purified by Ni"2"+-affinity chromatography, and used for in vitro assay. Tests on the substrate specificity of the His-tagged An-CsyA with myriad acyl-CoAs as starter substrates and malonyl-CoA as extender substrate showed that His-tagged An-CsyA accepted fatty acyl-CoAs (C2-C14) and produced triketide pyrones (C2-C14), tetraketide pyrones (C2-C10), and pentaketide resorcinols (C10-C14). Furthermore, acetoacetyl-CoA, malonyl-CoA, isobutyryl-CoA, and benzoyl-CoA were also accepted as starter substrates, and both of triketide pyrones and tetraketide pyrones were produced. It is noteworthy that the His-tagged An-CsyA produced polyketides from malonyl-CoA as starter and extender substrates and produced tetraketide pyrones from short-chain fatty acyl-CoAs as starter substrates. Therefore, this is the first report showing the functional properties of An-CsyA different from those of other fungal type III PKSs. -- Highlights: •Type III PKS from Aspergillus niger NRRL 328, An-CsyA, was cloned and characterized. •An-CsyA produced triketide pyrones, tetraketide pyrones and pentaketide resorcinols. •Functional properties of An-CsyA differs from those of other fungal type III PKSs.

  9. Synthesis of 14C-labelled α-methyl tyrosine

    International Nuclear Information System (INIS)

    Rajagopal, S.; Venkatachalam, T.K.; Conway, T.; Diksic, M.

    1992-01-01

    A new route for the preparation of radioactively labelled α-methyl L-tyrosine is described. The labelling at the α position has been successfully achieved with 14 C-, 11 C- (very preliminary, unpublished), and 3 H-labelled methyl iodide. A detailed report on 14 C-labelling at the α position and the hydrolysis of 4-methoxy α-methyl phenylalanine is presented. The alkylation proceeds via the methylation of the carbanion of N-benzylidene 4-methoxy phenylalanine methyl ester 2. Hydrolysis of 4-O methyl tyrosine to tyrosine by HBr and HI were analysed and used in the optimization of the hydrolysis conditions of 4. Enantiomeric purity of the isolated L-isomer has been found to be 99% as judged by HPLC. Pseudo first-order rate constant for the hydrolysis of 14 C-labelled α-methyl 4-methoxy phenyl alanine methyl ester was determined. Preliminary findings of the 3 H- and 11 C-radiolabelled α-methyl tyrosine (methyl labelled) are also mentioned. For the first time it was shown that α-methyl D,L-tyrosine can be separated into enantiomerically pure α-methyl D- and L-tyrosine using a CHIRALPAK WH column. (author)

  10. Measurements of in situ produced 14C in terrestrial rocks

    International Nuclear Information System (INIS)

    Yokoyama, Yusuke; Caffee, Marc W.; Southon, John R.; Nishiizumi, Kunihiko

    2004-01-01

    We developed and are testing a system for extracting in situ produced 14 C from quartz. 14 C is liberated from quartz matrix using step-wise heating during which time a spiked carrier gas consisting O 2 -CO-CO 2 -He is flowed through the high-temperature chamber continuously. The total 14 C background is reproducible and typically (2.3 ± 0.2) x 10 6 atoms, and the recovery is consistently greater than 90%. To validate the performance of the system and determine the blank level, we are using quartz samples taken from the Homestake mine (1600 m below the surface), South Dakota. To determine the 14 C release pattern and recovery, we used samples taken from the Transantarctic Mountains, Antarctica

  11. 40 CFR 721.10007 - Alcohols, C12-14-secondary, ethoxylated propoxylated.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alcohols, C12-14-secondary... New Uses for Specific Chemical Substances § 721.10007 Alcohols, C12-14-secondary, ethoxylated... identified as alcohols, C12-14- secondary, ethoxylated propoxylated (PMN P-00-11; CAS No. 103331-86-8) is...

  12. Effects of fertilizers, fungicides and herbicides on the fate of 14C-parathion and 14C-fonofos in soils and crops

    International Nuclear Information System (INIS)

    Lichtenstein, E.P.; Ferris, I.; Liang, T.T.; Koeppe, M.

    1983-01-01

    The fate of 14 C-parathion and 14 C-fonofos in soil is significantly affected by the presence of organic and inorganic fertilizers, fungicides and herbicides, possibly via the effect of soil microflora. Soil microorganisms are responsible for the oxidative as well as the reductive degradation of the insecticide. Using 14 carbon, the authors studied the effects of selected fungicides (benlate, captafol and manzate) herbicides (2,4-D parathion) and fertilizers ((NH 4 ) 6 SO 4 , KNO 3 , urea) on pesticides in Cromberry soils. Results of the study stress the importance of investigating the environmental fate of a particular pesticide in relation to the presence of the agricultural chemicals

  13. 14{sup C}-Metampicillin stability in several physiological

    Energy Technology Data Exchange (ETDEWEB)

    Jimeno, F; Casas, F; Carriazo, D

    1981-07-01

    Degradation of 14{sup C}-metampicillin incorporated to several physiological sera for medical uses has been studied. Influence of environmental conditions as well as possible interaction with the solvent have been specially analyzed. Degradation level of the labelled multiplication has been determined and its degradation products have been separated by using chromatographic and radiochemical methods. Likewise, the 14{sup C}-metam picill synthesis has been described. Finally, the results obtained have been discussed and evaluated. (Author) 9 refs.

  14. 14C-Metampicillin stability in several physiological sera

    International Nuclear Information System (INIS)

    Jimeno de Osso, F.; Casas Medica, F.; Carriazo Tovar, D.

    1981-01-01

    Degradation of 14 C -metampicillin incorporated to several physiological sera for medical uses has been studied. Influence of environmental conditions as well as possible interaction with the solvent have been specially analyzed. Degradation level of the labelled multiplication has been determined and its degradation products have been separated by using chromatographic and radiochemical methods. Likewise, the 14 C -metam picill synthesis has been described. Finally, the results obtained have been discussed and evaluated. (Author) 9 refs

  15. Preparative isolation of [U-14C]solanesol from 14CO2-chamber grown tobacco

    International Nuclear Information System (INIS)

    Hassam, S.B.

    1985-01-01

    A method for the preparative isolation of [U- 14 C]solanesol from 14 CO 2 -chamber grown tobacco is described. Freeze-dried tobacco leaves were Soxhlet extracted with methylene chloride. Fractionation of the extract by silica gel chromatography yielded crude solanesol. Subsequent purification by normal phase high pressure liquid chromatography yielded [U- 14 C]solanesol with a total activity of 474 μCi, a specific activity of 0.5 mCi/mmol, and a radiochemical purity of 95% as determined by RP-HPLC. The chemical purity was 97% and the chemical identity of the isolated compound was confirmed by co-chromatography with reference material and by mass spectroscopy. (author)

  16. Synthesis of oxindole from acetanilide via Ir(iii)-catalyzed C-H carbenoid functionalization.

    Science.gov (United States)

    Patel, Pitambar; Borah, Gongutri

    2016-12-22

    Herein we disclose the first report on the synthesis of oxindole derivatives from acetanilide via Ir(iii)-catalyzed intermolecular C-H functionalization with diazotized Meldrum's acid. A broad range of substituted anilides were found to react smoothly under the Ir(iii)-catalytic system to afford the corresponding N-protected oxindoles. The N-protecting groups, such as Ac, Bz or Piv, can be easily removed to furnish the oxindole. Various synthetic applications of the synthesized oxindole were also demonstrated.

  17. Method of preparing pyrimidine derivatives universally labelled with 14C

    International Nuclear Information System (INIS)

    Pritasil, L.; Filip, J.

    1976-01-01

    Sodium salts of beta-keto acid ethyl esters having mole activity higher than 40 mCi/milliatom 14 C are condensed with 14 C-thiourea having mole activity higher than 40 mCi/milliatom 14 C. Condensation proceeds in an anhydrous ethanol medium at a 1:1 molar ratio, with a 40 to 50% yield. Under the above reaction conditions, the radiochemical yield is higher than 20% while in biosynthesis it is 1% and in the chemical synthesis it is 10%. (J.P.)

  18. Distribution of 14C-activity among the organic acids in the Satsuma mandarin fruits fed with 14C-compounds

    International Nuclear Information System (INIS)

    Kubota, Shuji; Akao, Shoichiro; Hayashida, Michito.

    1978-01-01

    1. Twenty four hours after 14 CO 2 feeding to the leaves, malic acid had the highest level of total and specific radioactivity among the organic acids extracted from the juice vesicles, and citric acid had the second highest total activity. An unidentified acid compound had a relatively high activity. 2. Pyruvic acid-2- 14 C was fed as a substrate for acid formation to the one young fruit on a shoot, and NaH 14 CO 3 was fed as a source of carbon-dioxide to the other young fruit through the pedicel. After three hours of pyruvic acid feeding, malic acid, citric acid and aspartic acid were the major labelled compounds in the vesicles. Then, a marked increase and redistribution of activity in acids took place with time, and the levels of total and specific activity in citric acid increased steadily. The sorts of labelled compounds into which activity was incorporated from NaH 14 CO 3 were essentially similar to those in pyruvic acid-2- 14 C feeding. 3. These results seem to support the theory that the dark fixation of carbon-dioxide plays an important role in the synthesis of the organic acids in citrus fruit vesicles. (auth.)

  19. Distribution of 14C after oral administration of [1-14C]linoleic acid in rats fed different levels of essential fatty acids

    International Nuclear Information System (INIS)

    Becker, W.

    1984-01-01

    Rats from an inbred Sprague-Dawley strain were fed semisynthetic diets with a low [0.3 energy percent (en %)], normal (3 en %) or high (10 en %) content of essential fatty acids (EFA) for at least three generations. Twenty-nine- to 33-day-old male rats were given a single intragastric dose of [1-14C]linoleic acid in olive oil, and the respiratory CO2, urine and feces were collected for 46 hours (expt 1) or 20 hours (expt 2). The 14C activity in respiratory CO2, feces, urine and the carcass was determined in both experiments. In experiment 2 it was also measured in samples of the brown fat, liver, adrenals, white fat, skeletal muscles and brain. In both experiments the rats fed the low EFA diet retained significantly more 14C activity than the rats fed the normal or high EFA diets. In all groups the concentration of label was highest in the brown fat and the adrenals, but the above differences among the groups with respect to 14C retention were mainly observed in the liver, skeletal muscles and brain

  20. The distribution of 14C-chitosan by different molecular weight in mice

    International Nuclear Information System (INIS)

    Kim, Kwang Yoon; Kim, Young Ho; Bom, Hee Seung; Kim, Ji Yeul; Kim, Hee Kyung; Roh, Young Bok; Nishimura, Yoshikazu

    1998-01-01

    Chitosan is a nontoxic natural chealtor which was made by chitin, and reduced a contamination of radiostrontium in animals. In this experiment, a different molecular weight of C-14 chitosan was intravenously administered to mice, and then the distribution of C-14 chitosan in the body was observed. Male mice (8 to 10 weeks, body weight of 30 to 35g) of ICR strain were used. C-14 chitosan, mice was sacrificed at the 6th hour, 1st, 3rd, 5th, and 7th day. Beta radioactivities in the blood, liver, kidney, liver, muscle, testis, and urine was measured using a liquid scintillation analyzer. Most of the C-14 chitosan was excreted through urine within 6 hours. Biodistribution of C-14 chitosan was similar despite the difference of molecular weight. Higher distributions of radioactivities were found in the liver, kidney, spleen. The relative concentration in tissue increased for the 6 hours and then decreased. In conclusion, most of C-14 chitosan was excreted through urine despite the difference of molecular weight. and, low molecular weight of C-14 chitosan showed higher distribution than high molecular weight of C-14 chitosan in tissues

  1. Determination of the hydrothermal degradation products of D-(U-14C) glucose and D-(U-14C) fructose by TLC

    International Nuclear Information System (INIS)

    Bonn, G.; Bobleter, O.

    1983-01-01

    Hydrothermal degradation was examined using D-(U- 14 C) glucose and D-(U- 14 C) fructose. By thin layer chromatography with methylene chloride, tetrahydrofuran (THF), acetic acid - 60:20:20 as a mobile phase; it was possible to separate and identify the carbohydrates and their reaction products, glyceraldehyde, dihydroxyacetone, methylglyoxal, glycolaldehyde, 5-hydroxymethylfurfural and furfural. Up to 99% of the initial activity was determined by scintillation counting of the TL-chromatograms. A reaction scheme for the hydrothermal degradation of glucose and fructose was obtained from these results. (author)

  2. Method of preparing (U-14C)-D-galactose

    International Nuclear Information System (INIS)

    Zemek, J.; Kucar, S.; Kolina, J.

    1982-01-01

    Whole Chlorella algae cells cultivated in a 14 CO 2 medium were subjected to a β-galactosidase solution buffered to pH=4.5 to 6.0. The produced (U- 14 C)-D-galactose is separated by paper chromatography. (E.S.)

  3. Elaboración de corredores o canales endémicos mediante planillas de cálculo

    Directory of Open Access Journals (Sweden)

    Marcelo Bortman

    1999-01-01

    Full Text Available Las epidemias o brotes pueden ser definidos como un exceso en el número de casos de un problema de salud dado, en una población, un período y un lugar en particular. Sin embargo, determinar lo que constituye un exceso implica conocer lo que es normal o de esperar. La elaboración de canales o corredores endémicos permite definir los valores de casos esperados y de esta forma evidenciar de forma gráfica la aparición de un nú mero mayor de casos. En el presente trabajo se describe una nueva metodología para la realización de estos canales endémicos, en la que se utilizan las planillas de cálculo Qpro y Excel, mediante la determinación de la media geométrica de lastasas históricas y su in tervalo de confianza. Se presenta también un corredor endémico acumulativo que facilita la vigilancia de sucesos endémicos de baja incidencia.

  4. Model experiments for {sup 14}C water-age determinations

    Energy Technology Data Exchange (ETDEWEB)

    Wendt, I; Stahl, W; Geyh, M; Fauth, F [Bundesanstalt fuer Bodenforschung, Hannover (Germany)

    1967-05-15

    The {sup 14}C age of water samples is calculated by assuming that fossil carbonate is dissolved by biogenic CO{sub 2} according to the equation x{sub 1} {center_dot} CaCO{sub 3} + (x{sub 1}+y{sub 1}) {center_dot} CO{sub 2} + H{sub 2}O = 2x{sub 1} {center_dot} HCO{sub 3} + y{sub 1} {center_dot} CO{sub 2} where x and y are the number of moles of the two carbon components before and after the dissolution process. In a closed system the relation y{sub 1} = K(T) (x{sub 1}){sup 3} must be satisfied additionally. The equilibrium constant K(T), which depends on the temperature, controls the concentrations of free CO{sub 2} and HCO{sub 3}. To investigate the mechanism of the dissolution, laboratory experiments under controlled conditions were carried out. Non-radioactive CaCO{sub 3}, which had a {delta}{sup 13}C-value of +30 per mille, and radioactive CO{sub 2} with {delta}{sup 13}C = -22 per mille were used. The purpose of these investigations was to check the validity of theoretical assumptions regarding the average {sup 14}C-activity and the {delta}{sup 13}C-value of the total carbon which is dissolved as CO{sub 2} and HCO{sub 3}. Furthermore, it was investigated whether, within the duration of the experiment, a possible exchange takes place between the undissolved carbon present in the CaCO{sub 3} and that present in the HCO{sub 3}. The importance of this lies in the fact that the method of {sup 14}C age determination is based on the assumption that such an exchange does not take place. The experiments which have been performed up to now show that in case of the simple CaCO{sub 3} - CO{sub 2} system, which has been considered first, this assumption is not justified even for a constant water temperature. If variations in the water temperature occur during the history of the water sample, precipitation and redissolution processes influence the {sup 14}C- and {delta}{sup 13}C -values differently. This is due to isotopic fractionation processes between the HCO{sub 3} and CO

  5. Thermodynamic model for solution behavior and solid-liquid equilibrium in Na-Al(III-Fe(III-Cr(III-Cl-H2O system at 25°C

    Directory of Open Access Journals (Sweden)

    André Laurent

    2018-03-01

    Full Text Available The knowledge of the thermodynamic behavior of multicomponent aqueous electrolyte systems is of main interest in geo-, and environmental-sciences. The main objective of this study is the development of a high accuracy thermodynamic model for solution behavior, and highly soluble M(IIICl3(s (M= Al, Fe, Cr minerals solubility in Na-Al(III-Cr(III-Fe(III-Cl-H2O system at 25°C. Comprehensive thermodynamic models that accurately predict aluminium, chromium and iron aqueous chemistry and M(III mineral solubilities as a function of pH, solution composition and concentration are critical for understanding many important geochemical and environmental processes involving these metals (e.g., mineral dissolution/alteration, rock formation, changes in rock permeability and fluid flow, soil formation, mass transport, toxic M(III remediation. Such a model would also have many industrial applications (e.g., aluminium, chromium and iron production, and their corrosion, solve scaling problems in geothermal energy and oil production. Comparisons of solubility and activity calculations with the experimental data in binary and ternary systems indicate that model predictions are within the uncertainty of the data. Limitations of the model due to data insufficiencies are discussed. The solubility modeling approach, implemented to the Pitzer specific interaction equations is employed. The resulting parameterization was developed for the geochemical Pitzer formalism based PHREEQC database.

  6. An improved synthesis of 14C labelled glycerol using sodium borohydride

    International Nuclear Information System (INIS)

    Chander, H.; Ramamurthy, T.V.; Viswanathan, K.V.

    1987-01-01

    [1- 14 C]Glyceric acid has been reduced to [1(3)- 14 C]glycerol in high yields via the methyl ester of [1- 14 C]glyceric acid by sodium borohydride in the presence of t-butyl alcohol and methanol. The importance of the procedure is highlighted in relation to other procedures involving lithium aluminium hydride reduction. (author)

  7. Oxidation of propionic acid-3-14C with alkaline permanganate

    International Nuclear Information System (INIS)

    Zielinski, M.

    1981-01-01

    The mechanism of oxidation of propionic acid with permanganate in alkaline medium was reinvestigated using methyl- 14 C labelled propionate. The preferential rupture of the αC-βC bond in propionate in highly concentrated alkaline solutions of NaOH (and KOH) was confirmed and the appearance of 14 C-labelled oxalate explained by the formation of the symmetrical intermediate which decomposes in two different modes. (author)

  8. Indolenine meso-substituted dibenzotetraaza[14]annulene and its coordination chemistry toward the transition metal ions Mn(III), Fe(III), Co(II), Ni(II), Cu(II), and Pd(II).

    Science.gov (United States)

    Khaledi, Hamid; Olmstead, Marilyn M; Ali, Hapipah Mohd; Thomas, Noel F

    2013-02-18

    A new dibenzotetraaza[14]annulene bearing two 3,3-dimethylindolenine fragments at the meso positions (LH(2)), has been synthesized through a nontemplate method. X-ray crystallography shows that the whole molecule is planar. The basicity of the indolenine ring permits the macrocycle to be protonated external to the core and form LH(4)(2+)·2Cl(-). Yet another structural modification having strong C-H···π interactions was found in the chloroform solvate of LH(2). The latter two modifications are accompanied by a degree of nonplanar distortion. The antiaromatic core of the macrocycle can accommodate a number of metal ions, Mn(III), Fe(III), Co(II), Ni(II) and Cu(II), to form complexes of [Mn(L)Br], [Mn(L)Cl], [Fe(LH(2))Cl(2)](+)·Cl(-), [Co(L)], [Ni(L)], and [Cu(L)]. In addition, the reaction of LH(2) with the larger Pd(II) ion leads to the formation of [Pd(2)(LH(2))(2)(OAc)(4)] wherein the macrocycle acts as a semiflexible ditopic ligand to coordinate pairs of metal ions via its indolenine N atoms into dinuclear metallocycles. The compounds LH(2), [Co(L)], and [Ni(L)] are isostructural and feature close π-stacking as well as linear chain arrangements in the case of the metal complexes. Variable temperature magnetic susceptibility measurements showed thermally induced paramagnetism in [Ni(L)].

  9. Extraction of in situ cosmogenic 14C from olivine

    Science.gov (United States)

    Pigati, J.S.; Lifton, N.A.; Timothy, Jull A.J.; Quade, Jay

    2010-01-01

    Chemical pretreatment and extraction techniques have been developed previously to extract in situ cosmogenic radiocarbon (in situ 14C) from quartz and carbonate. These minerals can be found in most environments on Earth, but are usually absent from mafic terrains. To fill this gap, we conducted numerous experiments aimed at extracting in situ 14C from olivine ((Fe,Mg)2SiO4). We were able to extract a stable and reproducible in situ 14C component from olivine using stepped heating and a lithium metaborate (LiBO2) flux, following treatment with dilute HNO3 over a variety of experimental conditions. However, measured concentrations for samples from the Tabernacle Hill basalt flow (17.3 ?? 0.3 ka4) in central Utah and the McCarty's basalt flow (3.0 ?? 0.2 ka) in western New Mexico were significantly lower than expected based on exposure of olivine in our samples to cosmic rays at each site. The source of the discrepancy is not clear. We speculate that in situ 14C atoms may not have been released from Mg-rich crystal lattices (the olivine composition at both sites was ~Fo65Fa35). Alternatively, a portion of the 14C atoms released from the olivine grains may have become trapped in synthetic spinel-like minerals that were created in the olivine-flux mixture during the extraction process, or were simply retained in the mixture itself. Regardless, the magnitude of the discrepancy appears to be inversely proportional to the Fe/(Fe+Mg) ratio of the olivine separates. If we apply a simple correction factor based on the chemical composition of the separates, then corrected in situ 14C concentrations are similar to theoretical values at both sites. At this time, we do not know if this agreement is fortuitous or real. Future research should include measurement of in situ 14C concentrations in olivine from known-age basalt flows with different chemical compositions (i.e. more Fe-rich) to determine if this correction is robust for all olivine-bearing rocks. ?? 2010 by the Arizona

  10. Effect of Cold (14° C) vs. Ice (5° C) Water Immersion on Recovery From Intermittent Running Exercise.

    Science.gov (United States)

    Anderson, Daniel; Nunn, James; Tyler, Christopher J

    2018-03-01

    Anderson, D, Nunn, J, and Tyler, CJ. Effect of cold (14° C) vs. ice (5° C) water immersion on recovery from intermittent running exercise. J Strength Cond Res 32(3): 764-771, 2018-The purpose was to compare 14° C (CWI14° C) and 5° C (CWI5° C) cold water immersion after intermittent running. On 3 occasions, 9 male team-sport players undertook 12 minutes of CWI14° C, CWI5° C, or nonimmersed seated recovery (CON) after 45 minutes of intermittent running exercise. Maximal cycling performance and markers of recovery were measured before and in the 0-72 hours after exercise. Peak power output (PPO) was immediately reduced after all interventions (d = 1.8). CWI5° C was more effective at restoring PPO than CWI14° C (d = 0.38) and CON (d = 0.28) 24 hours after exercise, whereas both CON (d = 0.20) and CWI5 (d = 0.37) were more effective than CWI14° C after 48 hours. Cold water immersion (CWI) was more effective than CON at restoring PPO 72 hours after exercise (d = 0.28-0.30). Mean power output (MPO) was higher in CON compared with CWI5° C (d = 0.30) and CWI14° C (d = 0.21), but there was no difference between CWI5° C and CWI14° C (d = 0.08). CWI5° C was more effective than CWI14° C for restoring MPO to baseline levels 24 hours (d = 0.28) and 72 hours (d = 0.28) after exercise; however, CON was more, or equally, effective as CWI5° C and CWI14° C throughout. Lactate and creatine kinase concentrations were unaffected. Perceived muscle soreness remained elevated in CWI5 and CON throughout but was similar to baseline in CWI14° C after 72 hours. In conclusion, repeated bouts of exercise are initially impaired after 5 and 14° C CWI, but PPO may be improved 72 hours after exercise. Cold water immersion is not recommended for acute recovery based on these data. Athletes and coaches should use the time currently allocated to CWI for more effective and alternative recovery modalities.

  11. Synthesis of 14C and 32P double labelled triethylphosphine

    International Nuclear Information System (INIS)

    Kanska, M.; Drabarek, S.

    1979-01-01

    The synthesis of 14 C and 32 P double labelled triethylphosphine has been carried out using red phosphorus [ 32 P] and barium carbonate [ 14 C] as starting materials. The product of the reaction has been separated by gas chromatography. The 32 P radioactivity assay of the obtained product was performed by the liquid scintillation technique. The 14 C radioactivity was determined by the liquid scintillation technique and internal gas counting method. The radioactivity measurements have served to determine the total yield of double labelled triethylphosphine. (author)

  12. Impacts of C-uptake by plants on the spatial distribution of 14C accumulated in vegetation around a nuclear facility-Application of a sophisticated land surface 14C model to the Rokkasho reprocessing plant, Japan.

    Science.gov (United States)

    Ota, Masakazu; Katata, Genki; Nagai, Haruyasu; Terada, Hiroaki

    2016-10-01

    The impacts of carbon uptake by plants on the spatial distribution of radiocarbon ( 14 C) accumulated in vegetation around a nuclear facility were investigated by numerical simulations using a sophisticated land surface 14 C model (SOLVEG-II). In the simulation, SOLVEG-II was combined with a mesoscale meteorological model and an atmospheric dispersion model. The model combination was applied to simulate the transfer of 14 CO 2 and to assess the radiological impact of 14 C accumulation in rice grains during test operations of the Rokkasho reprocessing plant (RRP), Japan, in 2007. The calculated 14 C-specific activities in rice grains agreed with the observed activities in paddy fields around the RRP within a factor of four. The annual effective dose delivered from 14 C in the rice grain was estimated to be less than 0.7 μSv, only 0.07% of the annual effective dose limit of 1 mSv for the public. Numerical experiments of hypothetical continuous atmospheric 14 CO 2 release from the RRP showed that the 14 C-specific activities of rice plants at harvest differed from the annual mean activities in the air. The difference was attributed to seasonal variations in the atmospheric 14 CO 2 concentration and the growth of the rice plant. Accumulation of 14 C in the rice plant significantly increased when 14 CO 2 releases were limited during daytime hours, compared with the results observed during the nighttime. These results indicated that plant growth stages and diurnal photosynthesis should be considered in predictions of the ingestion dose of 14 C for long-term chronic releases and short-term diurnal releases of 14 CO 2 , respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Heating Changes Bio-Schwertmannite Microstructure and Arsenic(III Removal Efficiency

    Directory of Open Access Journals (Sweden)

    Xingxing Qiao

    2017-01-01

    Full Text Available Schwertmannite (Sch is an efficient adsorbent for arsenic(III removal from arsenic(III-contaminated groundwater. In this study, bio-schertmannite was synthesized in the presence of dissolved ferrous ions and Acidithiobacillus ferrooxidans LX5 in a culture media. Bio-synthesized Sch characteristics, such as total organic carbon (TOC, morphology, chemical functional groups, mineral phase, specific surface area, and pore volume were systematically studied after it was dried at 105 °C and then heated at 250–550 °C. Differences in arsenic(III removal efficiency between 105 °C dried-sch and 250–550 °C heated-sch also were investigated. The results showed that total organic carbon content in Sch and Sch weight gradually decreased when temperature increased from 105 °C to 350 °C. Sch partly transformed to another nanocrystalline or amorphous phase above 350 °C. The specific surface area of 250 °C heated-sch was 110.06 m2/g compared to 5.14 m2/g for the 105 °C dried-sch. Total pore volume of 105 °C dried-sch was 0.025 cm3/g with 32.0% mesopore and 68.0% macropore. However, total pore volume of 250 °C heated-mineral was 0.106 cm3/g with 23.6% micropore, 33.0% mesopore, and 43.4% macropore. The arsenic(III removal efficiency from an initial 1 mg/L arsenic(III solution (pH 7.5 was 25.1% when 0.25 g/L of 105 °C dried-sch was used as adsorbent. However, this efficiency increased to 93.0% when using 250 °C heated-sch as adsorbent. Finally, the highest efficiency for arsenic(III removal was obtained with sch-250 °C due to high amounts of sorption sites in agreement with the high specific surface area (SSA obtained for this sample.

  14. The synthesis of nucleoside bases with 14 C

    International Nuclear Information System (INIS)

    Matloubi, H.; Mehrdad, M.

    1997-01-01

    Labelled organic compounds have been widely and diligently applied to research problems in life science and chemistry. In many laboratories they have lost their novelty and have been become conventional research tools since long time ago. these applications frequently require organic compounds substituted (or labelled) with isotopes, but the isotopes are (with certain exception) extracted in first place in simple inorganic forms. The conversion of these simple form into the more or less complex labelled compounds called for by research workers has become in effect a new branch of practical organic chemistry. The preparation of labelled compounds, carbon-14 is probably more extensively and variously used than any other isotope. It emits only beta-particles. In this project, two kinds of nucleoside bases under the name uracil-2- 14 C and thymine (methyl- 14 C) were prepared.(author). 14 refs., 3 figs., 2 tabs

  15. Development of a C-14 detector and measurement of delta C-14 in dated tree rings grown in 1043 to 1055

    International Nuclear Information System (INIS)

    Oona, H.

    1979-01-01

    A proportional counter was constructed from plastic scintillator for measuring the C-14 contents in dendrochronologically dated tree ringas. The tree rings were individually converted to methane which, at one atmosphere pressure, was used as the counter gas. The wall, being a scintillator, serves as the 4π anti-coincidence shell for rejection of natural radioactivity in the material housing the proportional counter and penetrating cosmic ray muons. The output of the proportional counter, which is in anti-coincidence with the scintillation is recorded with a pulse height analyzer. After background subtraction, it yields the beta-decay spectrum of C-14 in the methane-filled proportional counter. The count rate obtained from the 5.5 liter effective volume counter for each year's sample is then referenced to a standard traceable to the National Bureau of Standards, and after corrections due to isotopic fracionation are applied, the ΔC-14 for each sample is determined. The fluctuations in the ΔC-14 are inspected, and used as an estimate for the energy content in the γ-ray burst of the Crab Nebula in 1054 A.D. Fluctuations due possibly to solar flares, neutron flux, cosmic ray muons, and sample preparation restrict the energy estimate to an upper limit of less than or equal to 10 50 ergs

  16. Biodegradation of {sup 14} C-atrazine under outdoor conditions; Biodegradacao de {sup 14} C-atrazina em condicoes semi controladas

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Brigida Pimentel Villar de

    1997-10-01

    Uniformly {sup 14} C-ring labeled atrazine (5 L/ha) was applied to a Typical Hapludox Brazilian Soil sample which was incubated under outdoor conditions. Sample of 200 g (dry weight base) of fresh soil were distributed in Erlenmeyer flasks and the moisture was adjusted for 2/3 rds of the soil field capacity. The flasks were then buried in the Lysimeter Station when they were incubated. The experiment started jointly with a corn planting. The {sup 14} C O{sub 2} was analyzed every 15 day, during a period of 150 days. The desorbed, extracted and bound residues were analyzed. The extracted soil was fractionated and the residues in the humin, fulvic and humic acids were determined. At the end of the incubation period (150 days), the {sup 14} CO{sub 2} evolved reached up to 36% of the total applied activity, the bound residues were detected in about the same (34%) during the inoculation period, and were distributed in the fractions of fulvic acids (29,91%), humic acids (6,83%) and humin (63,26%). The metabolites formed in the desorbed residues and in the extracted residues were determined using thin layer chromatography with {sup 14} C-detector. After 150 days incubation, desorbed soil residues were identified as atrazine (52,72%), hydroxiatrazine (44%) and desisopropilatrazine (3,28%). The extractable residues contained atrazine (79,29%), hydroxiatrazine (16,22%), desisopropilatrazine (2,25%) and desetylatrazine (2,24%). (author)

  17. An enzymic method for the determination of [1-14C] lactose

    International Nuclear Information System (INIS)

    Davies, E.; Bourke, E.; Costello, J.

    1975-01-01

    A simple, rapid and specific method for the determination of [1- 14 C] lactose in biological fluids is described. It is based on the enzymic removal of the 1- 14 C atom of lactose as [ 14 C] carbon dioxide, using commercially available enzymes. The assay involves only one critical addition and the entire reaction can be carried out in a scintillation vial. (author)

  18. Synthesis and analysis of the opioid analgesic [14C]-fentanyl

    International Nuclear Information System (INIS)

    Bagley, J.R.; Wilhelm, J.A.

    1992-01-01

    The synthesis of [ 14 C]-fentanyl, the radiolabelled congener of the potent opioid analgesic chosen for utilization in drug disposition studies, is described. [ 14 C]-Labelling was achieved in the first of two steps, a room temperature reduction of the in situ generated Schiff base from 1-phenylethyl-4-piperidone and [UL- 14 C]-aniline hydrochloride with sodium triacetoxyborohydride. A nearly instantaneous production of fentanyl was accomplished at room temperature with the addition of propionyl chloride. The overall radiochemical yield was 18%. The method described is efficiently adaptable for submicromolar scale while yielding a product of sufficient specific activity for in vivo studies. Our solvent system for thin layer chromatography was superior to the USP system reported for chromatographic analysis of fentanyl. This is the first reported preparation of [ 14 C]-fentanyl with the radiolabel in the aniline benzene ring. (author)

  19. HDL Subspecies Defined by Presence of Apolipoprotein C-III and Incident Coronary Heart Disease in Four Cohorts

    DEFF Research Database (Denmark)

    Jensen, Majken K; Aroner, Sarah A; Mukamal, Kenneth J

    2018-01-01

    Background -The causal role of high density lipoprotein (HDL) cholesterol in cardioprotection has been questioned by genetic and randomized studies. Novel measures that relate to HDL function may contribute new information to prediction of cardiovascular risk. Apolipoprotein C-III (apoC-III) is a......Background -The causal role of high density lipoprotein (HDL) cholesterol in cardioprotection has been questioned by genetic and randomized studies. Novel measures that relate to HDL function may contribute new information to prediction of cardiovascular risk. Apolipoprotein C-III (apo...... studies of adults free of CHD. In the Multi-Ethnic Study of Atherosclerosis (MESA), 5,657 participants (52% women; age 52-72 y) were followed for risk of CHD from 2000-2002 through 2013. In a case-cohort study nested within the Danish Diet, Cancer and Health (DCH) study, 3,642 participants (47% women; age.......87). Conclusions -Our findings from four prospective studies support the hypothesis that apoC-III may mark a subfraction of HDL that is associated with higher risk of CHD. New measures reflecting HDL structure and function may provide novel insights for cardiovascular risk that extend beyond traditional plasma HDL...

  20. Residues of {sup 14}C-paclobutrazol in mangoes

    Energy Technology Data Exchange (ETDEWEB)

    Costa, Maria A.; Tornisielo, Valdemar L.; Castanho, Giuliane M., E-mail: macosta@cena.usp.b [Centro de Energia Nuclear na Agricultura (CENA/USP), Piracicaba, SP (Brazil). Lab. de Ecotoxicologia

    2009-07-01

    Paclobutrazol (PBZ) is a growth regulator used in agricultural systems whose purpose is the control of vegetative growth, stimulating the reproductive capacity of plants. This growth regulator remains active in soil for a long time and its half-life varies with the type of soil and climatic conditions, can severely affect the development of crops. This work aimed to study the residues / metabolites of {sup 14}C-PBZ in mango pulp Tommy Atkins. The tests were performed with mangoes grown in pots stainless steel and application of {sup 14}C-PBZ was performed by the soil projection of the crown, and the mangoes tested in two periods, one year and two years after application. To evaluate the levels of residues of {sup 14}C-PBZ was realize the burning of 200 mg of pulp on biological oxidized and detached {sup 14}CO{sub 2} was detected by liquid scintillation spectrophotometer. The results were 1.65 % of residue of PBZ on fruit collected after two years of application and 4.30 % of residue of PBZ collected on fruit after a year of application and also can see that the product remained in the soil for more than one year, is translocated to the plant and reach the edible part, the pulp fruit. The identification of residual {sup 14}C- PBZ/metabolites by thin-layer chromatography did not reveal any pattern of PBZ / metabolites due to the low activity detected in the samples. Therefore, another procedure was performed for extraction and then analyzed by high performance liquid chromatography (HPLC) for detection of metabolites in the PBZ of mango pulp. (author)

  1. Techniques of tandem accelerator mass spectrometry and their applications to 14C measurements

    International Nuclear Information System (INIS)

    Nakamura, Toshio; Nakai, Nobuyuki; Furukawa, Michiaki

    1990-01-01

    A tandem accelerator mass spectrometer, named Tandetron was installed at Nagoya University in 1982 for 14 C measurement. The Tandetron spectrometer consists of a Cs sputter ion source to produce negative carbon ions, a Schenkel-type 2.2 MV tandem accelerator, an ion-beam analyzing apparatus with a charge-energy selector and mass spectrometer, and a heavy ion detector to identify and count 14 C 3+ ions from various background ions. The 14 C concentrations in pine needles, sampled at the Higashiyama Campus of Nagoya University, have been measured since 1984. The present article describes some of the measurements of 14 C in pine needles, focusing on the annual changes in the Δ 14 C value of atmospheric CO 2 , and on the effect upon 14 C concentrations for pine needles of a local 14 CO 2 emission from incineration of radioactive organic solvent wastes containing 14 C, at the Radioisotope Center in the Higashiyama Campus. The pine needles at some locations seemed to be influenced by local artificial CO 2 emission. The Δ 14 C values increased noticeably from 1956 to 1964 as a result of artificial 14 C produced in nuclear weapon tests. (N.K.)

  2. Synthesis of a polycyclic aromatic hydrocarbon marked with carbon-14: (b, d e f) dibenzo-chrysene {sup 14}C-7,14; Synthese d'un hydrocarbure aromatique polycyclique marque au carbone 14: le dibenzo (b, d e f) chrysene {sup 14}C-7,14

    Energy Technology Data Exchange (ETDEWEB)

    Chatelain, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    (b, d e f) dibenzo-chrysene C-7,14 has been synthesized from radioactive carbon dioxide and the organic magnesium compound derived from 1,5 dibromo naphthalene. The product has been purified by a very precise series of fractionated chromatographs on alumina having a chromatographic activity. This has necessitated the development of a special technique. (author) [French] Le dibenzo (b, d e f) chrysene 14C-7,14 a ete synthetise au depart de gaz carbonique radioactif et de bis-organomagnesien derive du dibromo-1,5 naphtalene. Le produit a ete purifie par une serie de chromatographies fractionnees sur alumine d'activite chromatographique tres precise. Ceci a fait l'objet d'une mise au point de technique. (auteur)

  3. Degradation of 14C-glyphosate in compost amended soils.

    Science.gov (United States)

    Alexa, E; Bragea, M; Sumalan, R; Negrea, M; Lazureanu, A

    2009-01-01

    Glyphosate (N-phosphonomethyl-glycine), the active ingredient in several herbicide formulations, is a non-selective, post-emergent herbicide used in a variety of crop and non-crop situations. Glyphosate is a non-volatile herbicide that is relatively immobile in soil. Its degradation is due to microbiological processes and most laboratory studies have been conducted with 14C-glyphosate with the rate of 14CO2 evolution being used as an indication of herbicide breakdown. In this paper we have studied the glyphosate degradation in compost amendment soils using Scientilator Liquid TRIATHLER and Glyphosate-phosphonomethyl-14C-labeled with specific activity 2,2mCi/mmol. Four types of soils have been taken under study: Black Chernozem, Vertisol, Gleysol and Phaeozem with different characteristics. For the each type of soil have been realized four experimental variants (glyphosate blind sample with 1,5 ppm, concentration, autoclaved soil, soil with glyphosate and addition of compost in field concentration of 40 t/ha, respectively 60 t/ha. The mineralization curves of 14CO2 accumulated were compared during of 40 days. All the mineralization curves for the soils exhibited same patterns, with only two phases, the initial rapid phase of degradation, for about 20 days, attributed to microbial action on the free glyphosate and the second slow phase, when the curves attained plateaus. Compost applied with different concentrations to Vertisol and Black Chernozem did not appear to stimulate the microbial degradation of glyphosate. In Gleysol and Phaeozem with lower humus content, the mineralization curve of 14C indicate the increase degradation capacity, expressed as accumulated 14CO2 as % total 14C, with the increase of compost concentration.

  4. MIN 14C UBT: A combination of gastric basal transit and 14C-urea breath test for the detection of helicobacter pylori infection in human beings

    International Nuclear Information System (INIS)

    Zubillaga, M.; Oliveri, P.; Calcagno, M.L.; Goldman, C.; Caro, R.; Mitta, A.; Degrossi, O.; Boccio, J.

    1997-01-01

    The purpose of this work is to demonstrate that the 14 C-urea breath test (UBT) performed at different times combined with the study of the gastric basal transit, which evaluates the intragastric displacement of a labeled solution under fasting conditions, has the advantage of being representative of the whole stomach surface and constitutes a non-aggressive test for the detection of H. pylori. This test, which has been called MIN 14 C UBT, is a modification of the conventional 14 C UBT in which low volumes of a solution of 14 C-urea together with 99m Tc-sulfur colloid are administered. The 99m Tc-sulfur colloid is not absorbed in the gastrointestinal tract and has the great advantage of allowing the 'visualization' of the transit of the 14 C-urea within the gastrointestinal tract. This modification allows the simultaneous determination of the production of the 14 CO 2 and the place where this process occurs. The results show that there is a good correlation between the images obtained and the breath samples collected. We found that this test has a sensitivity of 98% and a specificity of 96% for H. pylori detection

  5. 14 CFR 61.68 - Category III pilot authorization requirements.

    Science.gov (United States)

    2010-01-01

    ...) The addition of another type of aircraft to the applicant's Category III pilot authorization. (2) To... height, as applicable, including use of a radar altimeter; (iii) Recognition of and proper reaction to... an aircraft of the same category and class, and type, as applicable, as the aircraft for which the...

  6. Biokinetic studies on 14C-chitosan in rats

    International Nuclear Information System (INIS)

    Jia Minghong; Nishimura, Y.; Watanabe, Y.; Yukawa, M.

    1998-05-01

    The absorption and the basic metabolism of chitosan in rats are investigated. The results indicated that 14 C-chitosan from gastrointestinal tract was absorbed, metabolized and excreted quickly without re-bioavailability. The radioactive compounds perhaps with specifically chemical forms in serum, liver and the contents of small intestines were separated on GPC column and measured by radioactivity counting. A big pile of peaks with the retention volume almost same as that of standard 14 C-chitosan and another sharp one with the retention volume in the range of higher molecular weight same as that of BSA were discovered in analysis respectively for contents of intestine and serum or liver. The sharp peak would disappear if the proteins contained in the serum or liver were removed. In addition, and interesting tail peak, followed with the pile ones and eluted with the retention volume of lower molecular weight range same as that of chitooligosaccharides was also found in each of the 3 samples, ignoring the protein removal or not. These results suggested that most of 14 C-chitosan was not to be digested in intestine. On the other hand, a small amount of 14 C-chitosan was likely to be absorbed directly or after degraded to small molecular compounds into blood, liver and other tissues, and then connected with the proteins. Perhaps it is these trace materials that were playing important roles in reduction of the bioavailability of radiostrontium in rats

  7. Modified synthesis of 11-[{sup 14}C]-clozapine

    Energy Technology Data Exchange (ETDEWEB)

    Matloubi, Hojatollah E-mail: hmatloubi@seai.neda.net.ir; Ghandi, Mehdi; Zarrindast, M.-R.; Saemian, Nader

    2001-11-01

    The reported synthetic pathway of 8-chloro-11-(4-methyl-1-piperazinyl)-11-[{sup 14}C]-5H-dibenzo[b,e][1,4]diazapine (clozapine) was modified in several steps. The synthetic pathway was shortened by 60% and the total yield was increased from 6% to 23%.

  8. Formation constants of Sm(III), Dy(III), Gd(III), Pr(III) and Nd(III) complexes of tridentate schiff base, 2-[(1H-benzimidazol-2-yl-methylene) amino] phenol

    International Nuclear Information System (INIS)

    Omprakash, K.L.; Chandra Pal, A.V.; Reddy, M.L.N.

    1982-01-01

    A new tridentate schiff base, 2- (1H-benzimidazol-2-yl-methylene)amino phenol derived from benzimididazole-2-carbo-xaldehyde and 2-aminophenol has been synthesised and characterised by spectral and analytical data. Proton-ligand formation constants of the schiff base and metal-ligand formation constants of its complexes with Sm(III), Dy(III), Gd(III), Nd(III) and Pr(III) have been determined potentiometrically in 50% (v/v) aqueous dioxane at an ionic strength of 0.1M (NaClO 4 ) and at 25deg C using the Irving-Rossotti titration technique. The order of stability constants (logβ 2 ) is found to be Sm(III)>Dy(III)>Gd(III)>Pr(III)>Nd(III). (author)

  9. Formation constants of Sm(III), Dy(III), Gd(III), Pr(III) and Nd(III) complexes of tridentate schiff base, 2-((1H-benzimidazol-2-yl-methylene) amino) phenol

    Energy Technology Data Exchange (ETDEWEB)

    Omprakash, K L; Chandra Pal, A V; Reddy, M L.N. [Osmania Univ., Hyderabad (India). Dept. of Chemistry

    1982-03-01

    A new tridentate schiff base, 2- (1H-benzimidazol-2-yl-methylene)amino phenol derived from benzimididazole-2-carbo-xaldehyde and 2-aminophenol has been synthesised and characterised by spectral and analytical data. Proton-ligand formation constants of the schiff base and metal-ligand formation constants of its complexes with Sm(III), Dy(III), Gd(III), Nd(III) and Pr(III) have been determined potentiometrically in 50% (v/v) aqueous dioxane at an ionic strength of 0.1M (NaClO/sub 4/) and at 25deg C using the Irving-Rossotti titration technique. The order of stability constants (log..beta../sub 2/) is found to be Sm(III)>Dy(III)>Gd(III)>Pr(III)>Nd(III).

  10. AMS of {sup 14}C at low energies

    Energy Technology Data Exchange (ETDEWEB)

    Suter, M.; Huber, R.; Jacob, S. [ETHZ, Zurich (Switzerland); Synal, H.A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-09-01

    At the ETH/PSI AMS facility {sup 14}C test measurements have been performed at low terminal voltages of 0.5 and 1 MV in order to study the feasibility of AMS with very small accelerators. These experiments have demonstrated that interfering molecules ({sup 13}CH and {sup 12}CH{sub 2}) in charge states 1{sup +} and 2{sup +} can be destroyed in an adequate Ar gas stripper. These new results imply the feasibility of a new generation of very small accelerator systems for {sup 14}C. (author) 1 fig., 3 refs.

  11. Atmospheric 14C variations derived from tree rings during the early Younger Dryas

    Science.gov (United States)

    Hua, Quan; Barbetti, Mike; Fink, David; Kaiser, Klaus Felix; Friedrich, Michael; Kromer, Bernd; Levchenko, Vladimir A.; Zoppi, Ugo; Smith, Andrew M.; Bertuch, Fiona

    2009-12-01

    Atmospheric radiocarbon variations over the Younger Dryas interval, from ˜13,000 to 11,600 cal yr BP, are of immense scientific interest because they reveal crucial information about the linkages between climate, ocean circulation and the carbon cycle. However, no direct and reliable atmospheric 14C records based on tree rings for the entire Younger Dryas have been available. In this paper, we present (1) high-precision 14C measurements on the extension of absolute tree-ring chronology from 12,400 to 12,560 cal yr BP and (2) high-precision, high-resolution atmospheric 14C record derived from a 617-yr-long tree-ring chronology of Huon pine from Tasmania, Australia, spanning the early Younger Dryas. The new tree-ring 14C records bridge the current gap in European tree-ring radiocarbon chronologies during the early Younger Dryas, linking the floating Lateglacial Pine record to the absolute tree-ring timescale. A continuous and reliable atmospheric 14C record for the past 14,000 cal yr BP including the Younger Dryas is now available. The new records indicate that the abrupt rise in atmospheric Δ 14C associated with the Younger Dryas onset occurs at ˜12,760 cal yr BP, ˜240 yrs later than that recorded in Cariaco varves, with a smaller magnitude of ˜40‰ followed by several centennial Δ 14C variations of 20-25‰. Comparing the tree-ring Δ 14C to marine-derived Δ 14C and modelled Δ 14C based on ice-core 10Be fluxes, we conclude that changes in ocean circulation were mainly responsible for the Younger Dryas onset, while a combination of changes in ocean circulation and 14C production rate were responsible for atmospheric Δ 14C variations for the remainder of the Younger Dryas.

  12. Chemical Characteristics of C-14 Released from YGN-4

    Energy Technology Data Exchange (ETDEWEB)

    Kidoo Kang; Kyungrok Park; Kyoungdoek Kim; Jonghyun Ha [Nuclear Environment Technology Institute Korea Hydro and Nuclear Power Co., Ltd. P.O.Box 149, Yusung Daejeon, 305-600 (Korea, Republic of)

    2006-07-01

    Full text of publication follows: C-14 is resulting from the activation reaction of oxygen, nitrogen and carbon in the fuel and coolant of PWR. The amount of Carbon-14 released from PWR is small and not easy to detect, it is not used as a main monitored nuclide released in PWR in general. Korea Hydro and Nuclear Power Company (KHNP) had monitored Carbon-14 at five main ventilation lines of Yonggwang-4 from 2003 for 2 years. In order to monitor C-14, KHNP devised C-14 sampling instrument which can collect CO{sub 2} and hydrocarbons separately. It is composed of three main components, that is, primary CO{sub 2} sampler, a hydrocarbon oxidation assembly and a secondary CO{sub 2} sampler. The primary CO{sub 2} sampler has one water bubbler and two NaOH bubblers. To analyze C-14 in NaOH, CO{sub 3} ion was precipitated as CaCO{sub 3} or BaCO{sub 3} using CaCl{sub 2} and BaCl{sub 2} and performed mass analysis. But it was difficult due to over-precipitation by OH ion. This problem was solved by pH control using buffer solution NH{sub 4}Cl and adding some heat to the solution. The collecting efficiency was calculated to 92% and the test result was verified by C-14 tracer (NaHCO{sub 3}). According to the analysis results, the total activity is estimated to be 0.147 TBq/GWe.Yr. This activity would be about 67% of world's PWR average: 0.22 TBq/Gwe (UNSCEAR 2000) The area of highest concentration is the Fuel Building (RMS 035, which reaches 98% of total activity) followed by the Reactor Building, the Radwaste Building and the Auxiliary Building. The ventilation time of the Reactor Building is 3.3 hours per month, and 720 hours for the others (continuous) In the point of chemical form, the results show CO{sub 2} is dominant chemical form in fuel building, while methane compound is dominant in other areas. (authors)

  13. Development of adsorbent for C-14 Gas trapping and characteristics evaluation

    International Nuclear Information System (INIS)

    Park, Geun Il; Kim, I. T.; Kim, K. W.

    2006-08-01

    Desorption characteristics of C-14 adsorbed on spent resin as H 14 CO 3 ion type by applying various stripping solutions were analyzed, and some experiments for gasification of C-14 to CO 2 gas with were also performed. Based on these results, the process concept for spent resin treatment was suggested. Real spent resin was prepared from sampling in storage tank in site 1 of Wolseung Nuclear Power Plant. Desorption characteristics of C-14 and cations of Cs, Co from spent IRN-150 resin was evaluated. Desorption efficiency of C-14 from spent resin by using H 3 PO 4 desorption solution was over 96% regardless of C-14 amount on initial spent resin when comparing a activity of C-14 on initial spent resin. Also, desorption percent of cation of Cs, Co from anion ion-exchange resin (IRN-77) showed that Co-60 was below 1%, Cs-134, 137 was in a range of 2 ∼ 5%. Fundamental studies include an development of adsorbent manufacturing technology and its performance evaluation for C-14 gas trapping, the adsorption process by adopting gas circulation method was suggested for the design of 14 CO 2 gas treatment system generated from spent resin treatment process. In order to predict adsorbent performance of CO 2 trapping, modelling was carried out to verify the breakthrough curves of CO 2 trapping by using soda lime adsorbent. The effect of humidity on CO 2 trapping by using soda lime adsorbent was modelled via chemical reaction in porous media. Assessment of the state-of-the-arts on the solidification of the used adsorbent showed that the cement matrix would be the best-available binder from the view points of the matrix compatibility, properties of the final waste form, simplicity of the process and relatively low cost

  14. Rapid increase in cosmogenic 14C in AD 775 measured in New Zealand kauri trees indicates short-lived increase in 14C production spanning both hemispheres

    Science.gov (United States)

    Güttler, D.; Adolphi, F.; Beer, J.; Bleicher, N.; Boswijk, G.; Christl, M.; Hogg, A.; Palmer, J.; Vockenhuber, C.; Wacker, L.; Wunder, J.

    2015-02-01

    In 2012, Miyake et al. reported a sudden and strong increase of the atmospheric radiocarbon (14C) content in Japanese cedar trees of 1.2% between AD 774 and 775. While their findings were quickly confirmed by a German oak chronology for the Northern Hemisphere (NH), the question remained if the effect was seen in both hemispheres. Here we present the first annually resolved Southern Hemisphere (SH) 14C record spanning the interval AD 760-787, using New Zealand kauri (Agathis australis) chronology wood. An almost identical distinct increase compared to Northern Hemisphere data was observed, suggesting a cosmic event with globally uniform impact as a potential cause for the increase. Deploying a carbon cycle box model a worldwide averaged net 14C production of 2.2 ×108 14C atoms cm-2 was estimated, which is 3.7 times higher than the average annual 14C production. The immediate appearance of the event in tree rings on both hemispheres suggests a short duration event of significantly less than 1 yr.

  15. In vitro transfer rate of 14C from acetate-1-14C into ovarian steroids in the rat ovary during the estrous cycle and effects of LH and FSH

    International Nuclear Information System (INIS)

    Kimura, F.; Ishida, S.; Seto, K.; Kawakami, M.

    1976-01-01

    Fluctuations of ovarian biosynthetic activity and effects of exogenous LH and FSH on it during the estrous cycle were investigated by measuring in vitro transfer rates of 14 C from 14 C-1-acetate into progesterone (P), 20α-hydroxy-pregn-4-en-3-one (20α-OH-P) and estrogen (estradiol and estrone, E) in the ovarian homogenates from rats autopsied at 2 hour intervals. The transfer rate of 14 C from 14 C-1-acetate into P was lowest in the afternoon of estrus and increased from the morning of diestrus 1, making its peaks during the afternoon of diestrus 2 and in the midnight of proestrus. The transfer of 14 C into 20α-OH-P was high on the days of diestrus 2 and proestrus with its peak in the afternoon of the latter day. The maximum transfer of 14 C into E in the afternoon of proestrus and a high rate in the morning of estrus with relatively low one in the midnight were observed. Exogenously injected LH (150 μg) or FSH (150 μg) was eigther stimulatory or inhibitory to the transfer rates of 14 C from 14 C-1-acetate into ovarian steroids. During day time of diestrus 2 and midnight between proestrus and estrus, the transfer of 14 C into P and 20α-OH-P increased by LH, and during day time of proestrus and from the afternoon of estrus to the morning of diestrus 1 decreased. The transfr of 14 C into E increased by LH from the afternoon of diestrus 2 to the morning of proestrus, and decreased during the ofternoon of proestrus and from the afternoon of estrus to the morning of diestrus 2. Administration of FSH was also stimulatory or inhibitory. The 14 C transfer into P and 20α-OH-P increased by FSH from the afternoon of estrus to the morning of proestrus, but in the afternoon of proestrus they decreased. Transfer of 14 C into E increased by FSH significantly on the days of diestrus 2 and proestrus, and slightly on the day of estrus, while it decreased in the afternoon of diestrus 1. (author)

  16. The synthesis of [U-{sup 14}C phenyl] LS 840606, an agricultural fungicide

    Energy Technology Data Exchange (ETDEWEB)

    Madegard, G.; Mestre, P.; Raimond, P.; Noel, J.-P. [CEA Centre d`Etudes de Saclay, 91 - Gif-sur-Yvette (France)

    1995-12-01

    2,2`,4`-Trichloro-[ring U-{sup 14}C]acetophenone was the key intermediate of this synthesis patterned after the industrial route. An unexpected poor yield was observed during the preparation by the Friedel-Crafts reaction of chloroacetyl chloride with 1,3-dichloro-[U-{sup 14}C]benzene, possibly the result of an isotope effect although this poor yield might be explained by other factors. Two routes were checked for the preparation of 1,3-dichloro-[U-{sup 14} C]benzene. The action of CCl{sub 4} with 1,3-dinitro-[U-{sup 14} C]benzene at 280{sup o}C was entailed with explosions. A safer route started from [U-{sup 14}C]aniline via 2,4-dichloro-[ring U-{sup 14}C]acetanilide. Friedel-Crafts reaction with acetyl chloride gave rise in 52% yield to 2`,4`-dichloro-[ring U-{sup 14}C]acetophenone which was brominated to 2-bromo-2`,4`-dichloro-[ring U-{sup 14}C]acetophenone; was condensed with 2,2-(ethylenedioxy)etylmagnesium bromide to compound, was condensed with 1,2,4-triazole then successively treated with HCl:water:dioxane and 2,2,2-trifluoroethanol/HCl. Separation of the two diastereomers by medium pressure liquid chromatography. 7% overall radioactivity yield from [U-{sup 14}C]aniline. Radiochemical purity 99%. (author).

  17. Tracer experiment administering L-phenylalanine-U-14C and L-tyrosine-U-14C to the tissue slices of bamboo shoots

    International Nuclear Information System (INIS)

    Kozukue, E.; Mizuno, S.

    1987-01-01

    Uniformly 14 C-labeled L-phenylalanine and L-tyrosine were administered to tissue slices of both top and base sections of bamboo shoots. Alcohol soluble substances were extracted and then separated into organic acid, sugar and amino acid fractions by ion exchange chromatography. The homogentisic acid fraction among the organic acids was collected by high-performance liquid chromatography (HPLC) and its radioactivity was measured, while the alcohol insoluble residue was used for the analysis of lignin aldehyde by the method of alkaline nitrobenzene oxidation. 1. The two labeled amino acids were steadily incorporated into the tissues during incubation and rapidly converted to organic acid, sugar and alcohol insoluble residue, especially the latter. 2. On determining the amount of phenylalanine converted to tyrosine, it was found that this was extremely small. 3. The incorporation of phenylalanine-U- 14 C into alcohol insoluble residue was higher than that of tyrosine in both sections. 4. Although the conversion into lignin aldehyde from phenylalanine-U- 14 C was higher than that from tyrosine-U- 14 C, it was found that tyrosine incorporated into the shoots was converted to a remarkable extent for formation of lignin aldehyde. 5. The incorporation of phenylalanine and tyrosine into homogentisic acid was very low. From these results, we assume that the conversion of phenylalanine to tyrosine or of tyrosine to homogentisic acid is very small, and that a part of the high amount of tyrosine in the shoots may be used for formation of lignin

  18. Synthesis of steroids {sup 14}C-4: acetates of 19-nor-testosterone and testosterone; Syntheses de steroides {sup 14}C-4: acetates de 19-nor-testosterone et de testosterone

    Energy Technology Data Exchange (ETDEWEB)

    Floch, H

    1962-07-01

    The acetates of 19-nor-testosterone 4-{sup 14}C and testosterone 4-{sup 11}C have been prepared from ICH{sub 3}H{sub 8} {sup 14}C with respective yields of 32 percents and 56 percents in report of ICH{sub 3}-{sup 14}C. The cyclization in acid medium has given correct yields in opposition with the cyclization in alkaline medium that gives low yields for the testosterone and negative yields for the 19-nor-testosterone. [French] Les acetates de 19-nortestosterone 4-{sup 14}C et de testosterone 4-{sup 11}C ont ete prepares a partir de l'ICH{sub 3}H{sub 8} {sup 14}C avec des rendements respectifs de 32 pour cent et de 56 pour cent par rapport a l'ICH{sub 3}-{sup 14}C. La cyclisation en milieu acide nous a donne de bons rendements contrairement a la cyclisation en milieu alcalin qui donne des rendements faibles pour la testosterone et negatifs pour la 19-nortestosterone. (auteur)

  19. Complexes of lanthanum(III), cerium(III), samarium(III) and dysprosium(III) with substituted piperidines

    Energy Technology Data Exchange (ETDEWEB)

    Manhas, B S; Trikha, A K; Singh, H; Chander, M

    1983-11-01

    Complexes of the general formulae M/sub 2/Cl/sub 6/(L)/sub 3/.C/sub 2/H/sub 5/OH and M/sub 2/(NO/sub 3/)/sub 6/(L)/sub 2/.CH/sub 3/OH have been synthesised by the reactions of chlorides and nitrates of La(III), Ce(III), Sm(III) and Dy(III) with 2-methylpiperidine, 3-methylpiperidine and 4-methylpiperidine. These complexes have been characterised on the basis of their elemental analysis, and IR and electronic reflectance spectra. IR spectral data indicate the presence of coordinated ethanol and methanol molecules and bidentate nitrate groups. Coordination numbers of the metal ions vary from 5 to 8. 19 refs.

  20. Preparation of 2-(. alpha. -(2-ethoxyphenoxy)benzyl)-(5- sup 14 C)morpholine methanesulfonate (( sup 14 C)reboxetine):a new antidepressant agent

    Energy Technology Data Exchange (ETDEWEB)

    Angiuli, P.; Fontana, E.; Vicario, G.P. (Farmitalia Carlo Erba s.r.l., Milan (Italy))

    1991-05-01

    The labelling with radiocarbon of the new antidepressant agent Reboxetine is described. The preparation has been carried out in a two step procedure using 2-chloro-N-(3-(2-ethoxyphenoxy)-2-hydroxy-3-phenyl)propyl-(1-{sup 14}C)acetamide as starting material. The expected compound was prepared by cyclization of the above halogenoacylamido alcohol to the corresponding morpholone ring followed by reduction to the final (5-{sup 14}C)morpholine derivative 4, 98% radiochemically pure and with specific radioactivity of 988 MBq/mmol. An overall radiochemical yield of 57.5% was achieved. (author).

  1. Thermodecomposition of lanthanides (III) and ytrium (III) glucoheptonates

    International Nuclear Information System (INIS)

    Giolito, J.

    1987-01-01

    The lanthanides (III) and yttrium (III) glucoheptonates as well the D-glucoheptono 1-4 lactone were studied using common analytical methods, elemental microanalysis of carbon and hydrogen, thermogravimetry and differential scanning calorimetry. These compounds were prepared from the reaction between the lanthanides (III) and yttrium (III) hydroxides and glucoheptonic acid aqueous solution obtained by means of the delta lactone hydrolysis of this acid. After stoichiometric reaction the compounds were precipitated by the addition of absolute ethanol, washed with the same solvent and dried in desiccator. Thermogravimetric the (TG) curves of the lanthanides glucoheptonates of the ceric group present thermal profiles with enough differences permitting an easy caracterization of each compound and the yttrium (III) glucoheptonate TG curve showed a great similarity with the erbium (III) compound TG curve. The differential scanning calometry (DSC) curves showed endothermic and exothermic peaks by their shape, height and position (temperature) permit an easy and rapid identification of each compound specially if DSC and TG curves were examined simultaneously. (author) [pt

  2. Synthesis of (9Z, 12E-, (9E, 12Z-[1-14C]-linoleic acid, (9Z, 12Z, 15E-, (9E, 12Z, 15Z-[1-14C]-linolenic acid and (5Z, 8Z, 11Z, 14E-[1-14C]-arachidonic acid

    Directory of Open Access Journals (Sweden)

    Enard, Thierry

    1996-04-01

    Full Text Available Trans polyunsaturated fatty acids are produced in vegetable oils during heat treatment (240-250 °C.ln order to study the metabolic pathway of 9c, 12t and 9t, 12c linoleic acid and 9c, 12c, 15t and 9t, 12c, 15c linolenic acid, these products were prepared labelled with carbon 14 in the carboxylic position. 5c, 8c, 11c, 14t-Arachidonic acid was also labelled on the carboxylic position with carbon 14 in order to study its physiological effects. To introduce the labelling (E-bromo precursors with a 17 carbons chain or a 19 carbon chain were needed. The different syntheses were done by elongation steps and creation of cis double bonds via highly stereospecific Wittig reactions. The radioactive carbon atom was introduced from [14C]-potassium cyanide. The final radioactive fatty acids had a specific activity greater than 50 mCi/mmol and a radioactive purity better than 99 % for linoleic and linolenic and better than 98.6 % for arachidonic acid.

  3. Preparation of 14C-labelled poly(l-menthyl isopropenyl carbonates)

    International Nuclear Information System (INIS)

    Comes, R.A.; Grubbs, H.J.

    1981-01-01

    The synthesis of 14 C-labelled poly(l-menthyl isopropenyl carbonate) is described. Experimental conditions are included for incorporation of 14 C into each of the carbon atoms in the molecule. High pressure liquid chromatography conditions are given for separation and purification of the labelled intermediates. (author)

  4. Uptake of (2-/sup 14/C)abscisic acid and distribution of /sup 14/C in apple embryos

    Energy Technology Data Exchange (ETDEWEB)

    Barthe, P.; Bulard, C.

    1981-01-01

    Pyrus malus L. var. Golden delicious embryos were incubated with (+-)-(2-/sup 14/C) abscisic acid (ABA). After incubations of various durations, the radioactivity was measured in whole embryos, cotyledons, and embryonic axes. With either 48-h or 16-d incubation periods, the uptake of (/sup 14/C) ABA depended upon the mode of culture used. The lowest values corresponded to the absorption by the embryonic axis, the highest to the absorption by the distal parts of the two cotyledons. The cotyledons accumulated the main part of the radioactivity under all conditions. Dormant and almost completely after-ripened embryos cultivated for 4 d showed no significant differences in the radioactivity uptake for identical modes of culture. There was a linear relationship between exogenous ABA concentrations (0.5 to 3.10/sup -5/ M) and ABA uptake for embryos cultivated for 4 d with the distal parts of the cotyledons immersed in the medium.

  5. Biokinetics and dosimetry of radioactively labelled organic C-14 compounds

    International Nuclear Information System (INIS)

    Krins, A.; Sahre, P.; Schoenmuth, T.

    2003-12-01

    The report starts with summarising research work and the resulting scientific information in connection with the dosimetry of C-14 labelled organic compounds. Biokinetic models are developed for compounds such as benzene, phenol, aniline, nitrobenzene, and a selection of pharmaceuticals, in order to show the radioactivity distribution after administration of the C-14 labelled substances. Based on the those models, dose coefficients and excretion rates are derived. The following synoptic view of the available data library leads on to a discussion of various aspects, as eg. the question of whether and how monitoring for detection of incorporation of C-14 administered with labelled organic compounds is possible. None of the questions and aspects arising in connection with this subject can be adequately dealt with in the present document, but concepts and methods are presented which permit an interpretation of radioactivity excretion data measured after incorporation of C-14 labelled organic substances. (orig./CB) [de

  6. Effect of x irradiation on the biochemical maturation of rat cerebellum: Metabolism of [14C]glucose and [14C]acetate

    International Nuclear Information System (INIS)

    Patel, A.J.; Balazs, R.

    1975-01-01

    The effect was studied of selective x-irradiation of the cerebellum (100 R daily in the first 10 days after birth) on the maturation of glucose metabolism and the development of metabolic compartmentation, in 10-, 16-, and 23-day-old rats by using, respectively, [2- 14 C]glucose and [1- 14 C] acetate (40 μ Ci/100 g body weight each) as precursors. At day 10 significant changes, in comparison with the unirradiated controls, were observed: aspartate and γ-aminobutyrate, respectively, contained 36 percent and 64 percent more and glutamine 42 percent less glucose-carbon combined in amino acids; the glutamine/glutamate specific radioactivity ratio (RSA) was 25 percent less, and the conversion of both glucose and acetate carbons into acid-insoluble constituents was markedly reduced. However, in the postirradiation period both the conversion of glucose carbon into amino acids, and the RSA of glutamine after the administration of [ 14 C]acetate increased in a more or less normal fashion, although certain quantitative differences were noted. It seems, therefore, that the normal progress of biochemical differentiation was only affected to a small degree by the irradiation of the cerebellum, although the treatment interfered severely with cell proliferation. (U.S.)

  7. Comparing acquired angioedema with hereditary angioedema (types I/II): findings from the Icatibant Outcome Survey.

    Science.gov (United States)

    Longhurst, H J; Zanichelli, A; Caballero, T; Bouillet, L; Aberer, W; Maurer, M; Fain, O; Fabien, V; Andresen, I

    2017-04-01

    Icatibant is used to treat acute hereditary angioedema with C1 inhibitor deficiency types I/II (C1-INH-HAE types I/II) and has shown promise in angioedema due to acquired C1 inhibitor deficiency (C1-INH-AAE). Data from the Icatibant Outcome Survey (IOS) were analysed to evaluate the effectiveness of icatibant in the treatment of patients with C1-INH-AAE and compare disease characteristics with those with C1-INH-HAE types I/II. Key medical history (including prior occurrence of attacks) was recorded upon IOS enrolment. Thereafter, data were recorded retrospectively at approximately 6-month intervals during patient follow-up visits. In the icatibant-treated population, 16 patients with C1-INH-AAE had 287 attacks and 415 patients with C1-INH-HAE types I/II had 2245 attacks. Patients with C1-INH-AAE versus C1-INH-HAE types I/II were more often male (69 versus 42%; P = 0·035) and had a significantly later mean (95% confidence interval) age of symptom onset [57·9 (51·33-64·53) versus 14·0 (12·70-15·26) years]. Time from symptom onset to diagnosis was significantly shorter in patients with C1-INH-AAE versus C1-INH-HAE types I/II (mean 12·3 months versus 118·1 months; P = 0·006). Patients with C1-INH-AAE showed a trend for higher occurrence of attacks involving the face (35 versus 21% of attacks; P = 0·064). Overall, angioedema attacks were more severe in patients with C1-INH-HAE types I/II versus C1-INH-AAE (61 versus 40% of attacks were classified as severe to very severe; P types I/II, respectively. © 2016 British Society for Immunology.

  8. Poly[di-μ4-benzene-1,4-dicarboxylato-μ6-succinato-diholmium(III

    Directory of Open Access Journals (Sweden)

    Qin He

    2008-01-01

    Full Text Available The title compound, [Ho2(C4H4O4(C8H4O42]n, was synthesized hydrothermally. The Ho atom is coordinated by four O atoms from four benzene-1,4-dicarboxylate (BDC anions and four O atoms from three succinate anions, in a distorted square-antiprismatic coordination geometry. The antiprisms are bridged by the benzene-1,4-dicarboxylate and succinate anions, into a three-dimensional coordination network. The succinate anions are located on centres of inversion.

  9. Spectrophotometric determination of La (III) with sulphamethoxazole based hydroxy triazene

    International Nuclear Information System (INIS)

    Manwani, Sapana; Chauhan, R.S.; Goswami, A.K.

    2015-01-01

    In the present study, 3-hydroxy-3-p-chlorophenyll-1-(4-amino-N-(5-methyl-1,2-oxazole-3- yl) benzenesulphonamide-methane) triazene has been synthesized by coupling of hydroxylamine obtained by reduction of nitro compound with diazonium salt obtained from sulphamethoxazole taking hydroxylamine in excess at temperature between 0-5°C. Chemical structure of the synthesized compound was confirmed by IR, 1 H NMR, MASS and by elemental analysis. The complex of the reagent with La (III) has been studied. 3-hydroxy-3-p-chlorophenyll-1-(4-amino-N-(5-methyl-1,2-oxazole-3-yl) benzenesulphonamide-methane) triazene has been used for spectrophotometric determination of lanthanum (III) at 392 nm, keeping the pH between 8.5 to 8.9

  10. Metabolism of 4-/sup 14/C-dehydroepiandrosterone and 4-/sup 14/C-4-Androstene-3, 17-dione by isolated cells of early human placenta

    Energy Technology Data Exchange (ETDEWEB)

    Dziadkowiec, I; Czarnik, Z; Rembiesa, R [Department of Endocrinology, Institute of Pharmacology, Polish Academy of Sciences, Krakow

    1977-03-01

    The preparation of isolated cells was used for the study of the metabolism of 4-/sup 14/C-dehydroepiandrosterone and 4-/sup 14/C-4-androstene-3,17-dione in early human placenta. Free cell suspension converted dehydroepiandrosterone and 4-androstene-3,17-dione into estrone, estradiol-17..beta.., 4-androstene-3,17-dione and testosterone.

  11. {sup 14} C dating by using mass spectrometry with particle accelerator; Datacao por {sup 14} C utilizando espectrometria de massa com acelerador de particulas

    Energy Technology Data Exchange (ETDEWEB)

    Santos, G.M.; Gomes, P.R.S. [Universidade Federal Fluminense, Niteroi, RJ (Brazil). Inst. de Fisica]. E-mail: paulogom@if.uff.br; Yokoyama, Y. [Australian National Univ., Canberra (Australia). Research School of Earth Science; Tada, M.L. di; Cresswell, R.G.; Fifield, L.K. [Australian National Univ., Canberra (Australia). Dept. of Nuclear Physics

    1999-03-01

    The different aspects concerning the {sup 14} C dating are described, including the cosmogenic origin of {sup 14} C, its production and absorption by matter, the procedures to be followed for the age determination and the associated errors, particularly by the Accelerator Mass Spectrometry (AMS) technique, and the different steps of the sample preparation process. (author)

  12. The Determination of Sub-Microgram Quantities, of Amino Acids with H{sup 3}- and C{sup 1}4-Labelled 1-Fluoro-2.4 Dinitrobenzene; Determination d'acides amines en quantites inferieures au microgramme a l'aide de 1-fluoro-2,4-dinitrobenzen e marque au {sup 3}H et au {sup 14}C; Podschet submikrogrammnykh kolichestv aminokislot pri pomoshchi 2 : 4 dinitroftor'enzola, mechennogo H{sup 3} i C{sup 14}; Determinacion de cantidades de aminoacidos inferiores al microgramo por medio de 1-fluoro-2,4-dinitrobenceno marcado con {sup 3}H y {sup 14}C

    Energy Technology Data Exchange (ETDEWEB)

    Beale, D; Whitehead, J K [Middlesex Hospital Medical School, London (United Kingdom)

    1962-01-15

    satisfactoriament con los valores que suministra el analisis por derivacion empleando anhidrido acetico marcado con {sup 3}H y con {sup 14}C, y con los que se obtienen mediante cromatografia de intercambio ionico. (author) [Russian] Opisyvaetsya metod izotopnogo derivatsionnogo analiza dlya opredeleniya aminokislot pri nizkom urovne v 10{sup -5} mikro-mol' v gidrolizatakh proteina. 2:4 djnitroftorbenzola-H{sup 3} (G) byl sintezirovan iz ' brombenzola-H{sup 3}(G) i 2 : 4 dinitroftorbenzola-C{sup 14}(G), kotoryj byl poluchen iz khlorbenzola-C{sup 14}(G). Metod analiza vklyuchaet obrabotku smesi amino-kislot tritirovannym reaktivom (udel'naya aktivnost' 12.8 mikro kyuri/mikro ehkvijalent) v shchelochnoj rastvore, k kotoromu prisoedinyaetsya primes' s izvestnoj aktivnost' (6000 raspadov v minutu) proizvodnykh 2 : 4 dinitrofenila , mechennogo S14. Posle rastvoryayushchej ehkstraktsii smeshannaya reaktsiya vydelyaet iz svoego sostava proizvodnye dinitrofinila dvumya putyami khromatografii na bumage i soderzhanie H''3 i C''1''4 kazhdoj kapli opredelyaetsya szhiganiem i gazovym podschetom. Podschet H''3 daet kolichestvo, ravnoe proizvodnoj DNK iz aminokisloty, otdelennoj ot osnovnoj smesi, a schet C''1''4 ukazyvaet na velichinu poter', poluchivshikhsya vo vremya analiza. Itogi, poluchennye v rezul'tate analiza 1 mikrogramma gidrolizovannogo insulina polnost'yu soglasuyutsya s velichinami, poluchennymi v rezul'tate derivatsionnogo analiza s ispol'zovaniem uksusnogo angidrida, mechennogo H{sup 3} i C{sup 14} i s pomoshch'yu khromotografii ionnogo obmena smol. (author)

  13. Effect of HF leaching on {sup 14}C dates of pottery

    Energy Technology Data Exchange (ETDEWEB)

    Goslar, Tomasz, E-mail: goslar@radiocarbon.pl [Faculty of Physics, Adam Mickiewicz University, ul. Umultowska 85, 61-614 Poznan (Poland); Poznan Radiocarbon Laboratory, ul. Rubiez 46, 61-612 Poznan (Poland); Kozlowski, Janusz [Institute of Archaeology, Jagiellonian University, ul. Golebia 11, 30-007 Krakow (Poland); Szmyt, Marzena [Institute for Eastern Studies, Adam Mickiewicz University, ul. 28 Czerwca 1956 nr 198, 61-486 Poznan (Poland); Czernik, Justyna [Poznan Radiocarbon Laboratory, ul. Rubiez 46, 61-612 Poznan (Poland)

    2013-01-15

    This paper presents the experiments with {sup 14}C dating of two potsherds, which contained carbon dispersed rather homogeneously in their clay fabric. After AAA treatment, the potsherds still appeared to be contaminated with young carbon, presumably connected with humic acids. To make removal of humic acids more effective, we treated the sherds with HF acid of different concentration. The {sup 14}C results obtained demonstrate that HF treatment indeed helps to remove humic contaminants, but it also mobilizes carbon bound to raw clay, which may make {sup 14}C dates too old. We conclude therefore, that using a simple combination of HF and AAA treatment seems insufficient in reliable {sup 14}C dating of carbon homogeneously dispersed in the volume of potsherds.

  14. Estudio mediante tres técnicas del módulo elástico de un material compuesto de Al(6061 con un alto contenido (40%vol de SiC

    Directory of Open Access Journals (Sweden)

    Fernández, R.

    2001-04-01

    Full Text Available The purpose of this investigation is to study the elastic behavior of a discontinuously reinforced composite material, Al(6061-40vol%SiC, by using three different procedures: Extensometry in uniaxial testing, pendulum elasticimeter, and propagation of acoustic signals in the material. The high ceramic content of this material provides it with a high stiffness without a significant increase in density. Because of this, the material is suitable as structural component in the automotive and aerospace industry.

    El objetivo de esta investigación es estudiar el comportamiento elástico de un material compuesto con refuerzo discontinuo, Al(6061-40vol%SiC, mediante tres técnicas diferentes: extensometría para ensayos uniaxiales convencionales, elasticímetro pendular y mediante medidas de la velocidad de propagación de señales acústicas en el material. El alto contenido de la fase cerámica en este material le confiere elevada rigidez sin que su densidad aumente significativamente por lo que lo hacen adecuado como material estructural en diversas aplicaciones en el sector del transporte (automoción, aerospacial.

  15. Disposition of [14C]γ-cyclodextrin in germ-free and conventional rats

    NARCIS (Netherlands)

    Bie, A.T.H.J. de; Ommen, B. van; Bär, A.

    1998-01-01

    The absorption, disposition, metabolism, and excretion of 14C-labeled γ-cyclodextrin ([14C]γ-CD) was examined in four separate experiments with Wistar rats. In experiment 1, [14C]γ-CD (25 μCi, 600 mg/kg body wt) was administered intravenously to four male and four female conventional rats. In

  16. Disposition of 14C-α-cyclodextrin in germ-free and conventional rats

    NARCIS (Netherlands)

    Ommen, B. van; Bie, A.T.H.J. de; Bär, A.

    2004-01-01

    The absorption, disposition, metabolism, and excretion of uniformly 14C-labeled α-cyclodextrin (14C-α-CD) was examined in four separate experiments with Wistar rats. In Experiment 1, 14C-α-CD (25μCi, 50mg/kg bw) was administered intravenously to four male and four female conventional rats. In

  17. Atorvastatin decreases apolipoprotein C-III in apolipoprotein B-containing lipoprotein and HDL in type 2 diabetes: a potential mechanism to lower plasma triglycerides

    NARCIS (Netherlands)

    Dallinga-Thie, Geesje M.; Berk-Planken, Ingrid I. L.; Bootsma, Aart H.; Jansen, Hans

    2004-01-01

    Apolipoprotein (apo)C-III is a constituent of HDL (HDL apoC-III) and of apoB-containing lipoproteins (LpB:C-III). It slows the clearance of triglyceride-rich lipoproteins (TRLs) by inhibition of the activity of the enzyme lipoprotein lipase (LPL) and by interference with lipoprotein binding to

  18. Biodegradation of 14 C-atrazine under outdoor conditions

    International Nuclear Information System (INIS)

    Queiroz, Brigida Pimentel Villar de

    1997-10-01

    Uniformly 14 C-ring labeled atrazine (5 L/ha) was applied to a Typical Hapludox Brazilian Soil sample which was incubated under outdoor conditions. Sample of 200 g (dry weight base) of fresh soil were distributed in Erlenmeyer flasks and the moisture was adjusted for 2/3 rds of the soil field capacity. The flasks were then buried in the Lysimeter Station when they were incubated. The experiment started jointly with a corn planting. The 14 C O 2 was analyzed every 15 day, during a period of 150 days. The desorbed, extracted and bound residues were analyzed. The extracted soil was fractionated and the residues in the humin, fulvic and humic acids were determined. At the end of the incubation period (150 days), the 14 CO 2 evolved reached up to 36% of the total applied activity, the bound residues were detected in about the same (34%) during the inoculation period, and were distributed in the fractions of fulvic acids (29,91%), humic acids (6,83%) and humin (63,26%). The metabolites formed in the desorbed residues and in the extracted residues were determined using thin layer chromatography with 14 C-detector. After 150 days incubation, desorbed soil residues were identified as atrazine (52,72%), hydroxiatrazine (44%) and desisopropilatrazine (3,28%). The extractable residues contained atrazine (79,29%), hydroxiatrazine (16,22%), desisopropilatrazine (2,25%) and desetylatrazine (2,24%). (author)

  19. Studies on the distribution of 14C-labelled PCB in the body, 4

    International Nuclear Information System (INIS)

    Nagao, Soshichi; Hosoya, Hideo

    1976-01-01

    This paper is a report of 14 C-PCB distribution series in animals. We reported the results of the distribution of 14 C-PCB from birds, fish and shell in the previous experiments, and we have obtained some results from present experiment. This time interperito neal injection of 14 C-PCB solution was carried to mice, and the results were as follows; Excretion of 14 C-PCB as radioactivity was at its maximum about 6 hr. after medication. Excretive ratio was 87.20% for 24 hr, but 72.43% of radioactivity was excreted within 12hr. The result of radiopaperchromatography showed that 14 C-PCB was not changeable in the fecus after medication, being Rf = 0.92 in comparison with standard 14 C-PCB. 14 C-PCB distributed throughout the body of mice in 24 hr. and at least remained over till 480 hr. in adipose tissues of mice after single medication. (auth.)

  20. Correlation of [14C]muscimol concentration in rat brain with anticonvulsant activity

    International Nuclear Information System (INIS)

    Matthews, W.D.; Intoccia, A.P.; Osborne, V.L.; McCafferty, G.P.

    1981-01-01

    Muscimol, an in vivo and in vitro GABA agonist, has anticonvulsant activity against bicuculline-induced seizures when given systemically to rats. To determine whether parent compound or a metabolite possessed the anticonvulsant activity, experiments were performed with [ 14 C]muscimol. Anticonvulsant activity was determined by the percent of animals protected against tonic forelimb extension induced by bicuculline. Brain and urine were analyzed for unchanged [ 14 C]muscimol by thin-layer chromatography. The time course of anticonvulsant activity and [ 14 C]muscimol concentration in brain after intravenous injection were similar. Peak brain concentration of [ 14 C]muscimol and maximal protection against bicuculline-induced seizures occurred simultaneously. These data suggest that intravenously administered [ 14 C]muscimol rapidly penetrates brain tissue and parent compound is responsible for antagonism of bicuculline-induced convulsions. (Auth.)

  1. Biosynthesis of 14C-labelled erucic acid by means of rape plants

    International Nuclear Information System (INIS)

    Meisgeier, G.; Eckert, H.; Mueller, H.

    1991-01-01

    For the biosynthetic preparation of 14 C-erucic adid (C 21 H 41 COOH) by means of rape plants cv. sollux the plants were supplied with 14 CO 2 and additionally fed with 14 C-Sodium acetate after anthesis. After saponification of the extracted lipids the erucic acid was isolated and purified. The substance was identified by gas chromatography. The incorporation of the applied radioactive (34 MBq 14 CO 2 ; 37 MBq 14 C-natrium acetate) into the fatty acids amounted to 1,2 per cent. The erucic acid could be isolated from the fatty acids mixture with a specific radioactivity of 1,001 MBq/mmol and a purity of 97,2 per cent. (orig.) [de

  2. Evaluation of surface dose rate on C-14 scrubber and gas bag

    International Nuclear Information System (INIS)

    Gang, D. W.; Lee, H. S.; Lee, D. H.

    2003-01-01

    In CANDU(Canadian Deuterium Uranium) reactors, purge and discharge of moderator cover gas has been performed via vapor recovery system. The methods employed in C-14 removal are mainly based on reactions of CO 2 with absorber of adsorbent. In order to choose an optimum process, we should consider the characteristics of the process, such as, temperature, pressure, humidity etc. and surface dose rate on C-14 scrubber and gas bag to estimate job-related personnel doses. Assuming that the whole C-14 scrubber was completely replaced after one-cycle operation, and that its C-14 activity for one-cycle operation was 40 mCi, we calculated the surface dose rate at the six points of the C-14 scrubber. This calculation showed that the dose rate on the surface of cartridge was only 1.25μSυ/hγ because of low energy of β ray. It is concluded, therefore, that the cartridge change-out is safe because the operation of C-14 removal system causes only a small increase in dose rate

  3. Atmospheric histories and growth trends of C4F10, C5F12, C6F14, C7F16 and C8F18

    Directory of Open Access Journals (Sweden)

    R. F. Weiss

    2012-05-01

    Full Text Available Atmospheric observations and trends are presented for the high molecular weight perfluorocarbons (PFCs: decafluorobutane (C4F10, dodecafluoropentane (C5F12, tetradecafluorohexane (C6F14, hexadecafluoroheptane (C7F16 and octadecafluorooctane (C8F18. Their atmospheric histories are based on measurements of 36 Northern Hemisphere and 46 Southern Hemisphere archived air samples collected between 1973 to 2011 using the Advanced Global Atmospheric Gases Experiment (AGAGE "Medusa" preconcentration gas chromatography-mass spectrometry systems. A new calibration scale was prepared for each PFC, with estimated accuracies of 6.8% for C4F10, 7.8% for C5F12, 4.0% for C6F14, 6.6% for C7F16 and 7.9% for C8F18. Based on our observations the 2011 globally averaged dry air mole fractions of these heavy PFCs are: 0.17 parts-per-trillion (ppt, i.e., parts per 1012 for C4F10, 0.12 ppt for C5F12, 0.27 ppt for C6F14, 0.12 ppt for C7F16 and 0.09 ppt for C8F18. These atmospheric mole fractions combine to contribute to a global average radiative forcing of 0.35 mW m−2, which is 6% of the total anthropogenic PFC radiative forcing (Montzka and Reimann, 2011; Oram et al., 2012. The growth rates of the heavy perfluorocarbons were largest in the late 1990s peaking at 6.2 parts per quadrillion (ppq, i.e., parts per 1015 per year (yr for C4F10, at 5.0 ppq yr−1 for C5F12 and 16.6 ppq yr−1 for C6F14 and in the early 1990s for C7F16 at 4.7 ppq yr−1 and in the mid 1990s for C8F18 at 4.8 ppq yr−1. The 2011 globally averaged mean atmospheric growth rates of these PFCs are subsequently lower at 2.2 ppq yr−1 for C4F10, 1.4 ppq yr−1 for C5F12, 5.0 ppq yr−1 for C6F14, 3.4 ppq yr−1 for C7F16 and 0.9 ppq yr−1 for C8F18. The more recent slowdown in the growth rates suggests that emissions are declining as compared to the 1980s and 1990s.

  4. Dissociation kinetics of Fe(III)- and Al(III)-natural organic matter complexes at pH 6.0 and 8.0 and 25 °C

    Science.gov (United States)

    Jones, Adele M.; Pham, A. Ninh; Collins, Richard N.; Waite, T. David

    2009-05-01

    The rate at which iron- and aluminium-natural organic matter (NOM) complexes dissociate plays a critical role in the transport of these elements given the readiness with which they hydrolyse and precipitate. Despite this, there have only been a few reliable studies on the dissociation kinetics of these complexes suggesting half-times of some hours for the dissociation of Fe(III) and Al(III) from a strongly binding component of NOM. First-order dissociation rate constants are re-evaluated here at pH 6.0 and 8.0 and 25 °C using both cation exchange resin and competing ligand methods for Fe(III) and a cation exchange resin method only for Al(III) complexes. Both methods provide similar results at a particular pH with a two-ligand model accounting satisfactorily for the dissociation kinetics results obtained. For Fe(III), half-times on the order of 6-7 h were obtained for dissociation of the strong component and 4-5 min for dissociation of the weak component. For aluminium, the half-times were on the order of 1.5 h and 1-2 min for the strong and weak components, respectively. Overall, Fe(III) complexes with NOM are more stable than analogous complexes with Al(III), implying Fe(III) may be transported further from its source upon dilution and dispersion.

  5. Use of natural diamonds to monitor 14C AMS instrument backgrounds

    International Nuclear Information System (INIS)

    Taylor, R.E.; Southon, John

    2007-01-01

    To examine one component of the instrument-based background in University of California Keck Carbon Cycle AMS spectrometer, we have obtained measurements on a set of natural diamonds pressed into sample holders. Natural diamond samples (N = 14) from different sources within rock formations with geological ages greatly in excess of 100 Ma yielded a range of currents (∼110-250 μA 12 C - where filamentous graphite typically yields ∼150 μA 12 C - ) and apparent 14 C ages (64.9 ± 0.4 ka BP [0.00031 ± 0.00002 fm] to 80.0 ± 1.1 ka BP [0.00005 ± 0.00001 fm]). Six fragments cut from a single diamond exhibited essentially identical 14 C values - 69.3 ± 0.5 ka-70.6 ± 0.5 ka BP. The oldest 14 C age equivalents were measured on natural diamonds which exhibited the highest current yields

  6. Heating of aluminum by SPR-III burst

    International Nuclear Information System (INIS)

    Judd, S.V.

    1987-01-01

    Real time temperature measurements were made on an aluminum cylinder exposed to radiation bursts at SPR-III at neutron levels from 10 11 cm -2 to 4.5 x 10 14 cm -2 . Precision thermistors and high speed A/D converters were used to measure temperature with .0025 degree C resolution at 20ms intervals following the burst. Temperature data is presented as a function of neutron fluence

  7. Preparation of phenyl, p-fluorophenyl, 2-thienyl {beta} alanines {beta} -{sup 14}C; Preparation de phenyl, p-fluorophenyl, thienyl-2 {beta} alanines {beta} - {sup 14}C

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L; Carbonnier, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1959-07-01

    Description of the synthesis of the amino acids given in the title, labelled with {sup 14}C in the beta position. Benzoic, fluorobenzoic and thenoic acids carboxyl {sup 14}C prepared from {sup 14}CO{sub 2} from converted respectively to benzyl chloride, p-fluorobenzyl chloride and 2-chloromethyl thiophene, which were condensed in dimethyl-formamide solution with sodium ethyl acetamido malonate. After hydrobromic hydrolysis the desired products were obtained with respective overall yields of 64, 49 and 57 per cent. (author) [French] Description de la synthese des acides amines du titre, marques au {sup 14}C en position beta. Les acides benzoique, fluorobenzoique, thenoique carboxyl {sup 19}C prepares a partir de {sup 14}CO{sub 2} ont ete transformes respectivement en chlorure de benzyle, chlorure de p-fluorobenzyle, chloromethyl-2 thiophene lesquels ont ete condenses dans le dimethyl-formamide sur l'acetamidomalonate d'ethyle sode. Apres hydrolyse bromhydrique, on a obtenu les produits cherches avec les rendements globaux respectifs de 64, 39 et 57 pour cent. (auteur)

  8. Synthesis of dexamethasone-4-14C

    International Nuclear Information System (INIS)

    Rao, P.N.; Cessac, J.W.; Hill, K.A.

    1982-01-01

    The bismethylenedioxy (BMD) derivative of dexamethasone 2 was silylated with trimethylchlorosilane and imidazole in dimethylformamide to give the 11β-trimethylsilyloxy BMD derivative 3. The Δ 1 -double bond in 3 was hydrogenated over 5% palladium on carbon to give the Δ 4 -3-oxo steroid 4. Oxidation of 4 with potassium permanganate-sodium metaperiodate gave the seco-acid 5 which on subsequent treatment with acetic anhydride; sodium acetate and triethylamine gave the enol-lactone 6. The enol-lactone 6 was reacted with 14 C-methylmagnesium iodide to give an adduct 7a which on heating at reflux with lithium 2,6-di-t-butylphenoxide in dioxane gave the Δ 4 -3-oxo derivative 8. Compound 8 was heated at reflux with m-iodylbenzoic acid and diphenyl diselenide in toluene to give the Δsup(1,4)-3-oxo steroid 9. The protecting BMD and silyl groups were removed in a single step by reaction with aqueous trifluoroacetic acid containing 2N hydrochloric acid at room temperature to give dexamethasone-4- 14 C 10. (author)

  9. A DFT study of thermodynamic properties of C36 and C14 Fe2Zr Laves phases

    Science.gov (United States)

    Ali, Kawsar; Ghosh, P. S.; Arya, A. K.

    2018-04-01

    Fe-Zr alloys are promising materials for metallic waste immobilization in nuclear industry. C36 and C14 Fe2Zr Laves phases are frequently observed in Fe-Zr alloys that can host radionuclides. The phonon dispersions of C36 and C14 Fe2Zr Laves phases shows that both intermetallics are dynamically stable. The Helmholtz free energy, vibrational entropy, internal energy and specific heat at constant volume has been calculated. The zero point energies of C36 and C14 phases are 9.23 and 9.91 kJ/mole, respectively. The vibrational free energy becomes negative at 250 K and 270 K. The high temperature specific heat at constant volume of both intermetallics is 74 J/K/mole.

  10. Effect of Cooking on 14C-Chloropyrifos Residues in Stored Faba Beans

    International Nuclear Information System (INIS)

    Mahdy, F.

    2006-01-01

    The effect of cooking on the amount and nature of 14 C-chloropyrifos residues in stored vicia faba beans was studied. faba beans treated with (ethyl-1- 14 C) chloropyrifos insecticide at a dose 15 and 45 mg insecticide/kg seeds and stored for 30 weeks had 50-54% of the actual applied doses inside the grains in the form of extractable and bound 14 C- chloropyrifos residues. Extractable residues in cooked beans included, in addition to the parent insecticide O-analogue, desethyl chloropyrifos and 3,5,6-trichloro pyridinol, as main degradation products of 14 C-chloropyrifos

  11. 14 C dating by using mass spectrometry with particle accelerator

    International Nuclear Information System (INIS)

    Santos, G.M.; Gomes, P.R.S.; Yokoyama, Y.; Tada, M.L. di; Cresswell, R.G.; Fifield, L.K.

    1999-01-01

    The different aspects concerning the 14 C dating are described, including the cosmogenic origin of 14 C, its production and absorption by matter, the procedures to be followed for the age determination and the associated errors, particularly by the Accelerator Mass Spectrometry (AMS) technique, and the different steps of the sample preparation process. (author)

  12. Synthesis and analysis of 14C-labelled butyltin compounds

    International Nuclear Information System (INIS)

    Kloetzer, D.

    1976-01-01

    This paper deals with methods for the synthesis of 14 C-labelled analoga of the important biocides tributyltin oxide, tributyltin benzoate, tributyltin salicylate and tributyltin fluoride as well as dibutyltin oxide. The radioactive starting substance butylbromide-1- 14 C is treated with sodium and monobutyltin chloride or tin tetrachloride to form a mixture of radioactive butyltin compounds from which the substance desired is separated. A system satisfactorily meeting the conditions for thin-layer radiochromatography is presented. (author)

  13. Radioactive decay of 223Ra by 14C emission

    International Nuclear Information System (INIS)

    Yashita, S.; Gregorich, K.; Ghiorso, A.

    1985-01-01

    Recently H.J. Rose and G.A. Jones at the University of Oxford reported the very difficult observation of an exotic radioactive decay mode in 233 Ra, its spontaneous disintegration by the emission of 14 C particles. The authors have confirmed their somewhat surprising discovery by an independent method. Within the present experimental accuracy the magnetic rigidity, energy and branching ratio support the assignment of 14 C emission from 223 Ra as proposed by the Oxford experiment

  14. Synthesis of phenobarbital 14C - 5 (1964)

    International Nuclear Information System (INIS)

    Benakis, A.

    1964-01-01

    Phenobarbital (Luminal), well known as a hypnotic agent, plays also an important role in the medical treatment of epilepsy. With the object of studying the metabolism of this medicament in the living system, the synthesis of phenobarbital marked in position 2 of the pyrimidinic ring has been effected. It has been necessary, in order to carry out to research into the metabolism of this product, to have a phenobarbital marked in position 5 of the pyrimidinic ring. This synthesis, making it possible to introduce C-14 into position 5 of the pyrimidinic ring, consists of seven stages starting from C-14 carboxyl benzoic acid having a specific activity of 25 mc/mM. The melting point of the final product is 172 - 173 deg. C and its specific activity is 11.15 mc/mM. The overall radioactive yield of the pure product, with respect to the original benzoic acid (10 mM) is of the order of 3 per cent. The purity of the product has been controlled by paper chromatography; it is of the order of 99 per cent. (author) [fr

  15. Associations among Race/Ethnicity, ApoC-III Genotypes, and Lipids in HIV-1-Infected Individuals on Antiretroviral Therapy.

    Directory of Open Access Journals (Sweden)

    2006-01-01

    Full Text Available BACKGROUND: Protease inhibitors (PIs are associated with hypertriglyceridemia and atherogenic dyslipidemia. Identifying HIV-1-infected individuals who are at increased risk of PI-related dyslipidemia will facilitate therapeutic choices that maintain viral suppression while reducing risk of atherosclerotic diseases. Apolipoprotein C-III (apoC-III gene variants, which vary by race/ethnicity, have been associated with a lipid profile that resembles PI-induced dyslipidemia. However, the association of race/ethnicity, or candidate gene effects across race/ethnicity, with plasma lipid levels in HIV-1-infected individuals, has not been reported. METHODS AND FINDINGS: A cross-sectional analysis of race/ethnicity, apoC-III/apoA-I genotypes, and PI exposure on plasma lipids was performed in AIDS Clinical Trial Group studies (n = 626. Race/ethnicity was a highly significant predictor of plasma lipids in fully adjusted models. Furthermore, in stratified analyses, the effect of PI exposure appeared to differ across race/ethnicity. Black/non-Hispanic, compared with White/non-Hispanics and Hispanics, had lower plasma triglyceride (TG levels overall, but the greatest increase in TG levels when exposed to PIs. In Hispanics, current PI antiretroviral therapy (ART exposure was associated with a significantly smaller increase in TGs among patients with variant alleles at apoC-III-482, -455, and Intron 1, or at a composite apoC-III genotype, compared with patients with the wild-type genotypes. CONCLUSIONS: In the first pharmacogenetic study of its kind in HIV-1 disease, we found race/ethnic-specific differences in plasma lipid levels on ART, as well as differences in the influence of the apoC-III gene on the development of PI-related hypertriglyceridemia. Given the multi-ethnic distribution of HIV-1 infection, our findings underscore the need for future studies of metabolic and cardiovascular complications of ART that specifically account for racial

  16. Uptake and metabolism of 14C-chloropyrifos by marine bivalves

    International Nuclear Information System (INIS)

    Zhong, C.G.; Chen, S.; Zhao, X.; Shi, J.; Carvalho, F.P.

    1999-01-01

    The uptake and metabolism of 14 C-chlorpyrifos by two marine bivalves, Paphia undulata and Sinonovacula constricta, were studied in a simulated ecosystem. The experiments were carried out in two 30 L glass tanks containing each 20 L of filtered sea water, contaminated with 14 C-chlorpyrifos 1.85x10 4 Bq.L -1 (16.7 μg.L -1 ) at the beginning of the exposure period. At different time intervals, three specimens of each species were sampled for analysis of the pesticide in the molluscs tissues. The 14 C-chlorpyrifos residues were extracted from the digestive gland of the molluscs and analyzed by co-chromatography with pesticide standards by TLC methods described before

  17. Temporal distribution of bomb 14C in a forest soil

    International Nuclear Information System (INIS)

    Harkness, D.D.; Harrison, A.F.; Bacon, P.J.

    1986-01-01

    Patterns of 14 C enrichment in the superficial plant debris and mineral soil horizons of an established woodland have been monitored at regular intervals during the past 15 years. These data are compared with a model evaluation of carbon turnover based on the recorded changes in atmospheric 14 C concentration since AD 1900. Leaf litter and decomposing plant debris are characterized by steady-state turnover values of ca 2 and ca 8 years, respectively. A two-component system of fast (≤20 yr) and slow (ca 350 yr) cycling carbon is indicated for the surface (0-5cm) soil humus; below 10cm, the fast component is rare ( 14 C to the soil carbon pool

  18. Absorption, distribution, metabolism and excretion of 14C-chlorphenesin carbamate in rats

    International Nuclear Information System (INIS)

    Nozu, Takashi; Aoyagi, Tadao; Setoyama, Kageyoshi; Suwa, Toshio; Tanaka, Ichiro

    1977-01-01

    Absorption, distribution, metabolism and excretion of chlorphenesin carbamate (CPC), a central acting muscle relaxant, were investigated in rats by use of 14 C-labeled CPC. After oral administration, 14 C-CPC was well absorbed from gastrointestinal tract and about 90% of the given radioactivity was excreted in urine and 5% in feces during 5 days. Approximately 36% was recovered in bile during 8 hr after oral administration. The highest blood level of 14 C was observed at 3-8 hr after oral administration and decreased slowly. The radioactivity was distributed widely in almost all tissues. The highest concentration of 14 C was observed in the liver and the higher was detected in the brain and spinal cord, suggesting a pharmacological effect of CPC. In pregnant rats given 14 C-CPC orally, the radioactivity in the fetuses was below 0.8% of the dose at 1-24 hr. The major metabolites in 48 hr urine was identified as CPC-glucuronide and the acidic metabolites, p-chlorophenoxylactic acid, p-chlorophenoxyacetic acid and p-chlorophenol, were also detected. After intravenous injection of the 14 C-labeled acidic metabolites, the radioactivity was not detected in the central nervous system and excreted rapidly. In the case of repeated administration of CPC and 14 C-CPC for 21 days, the radioactivity did not accumulated in any tissue of rats. (auth.)

  19. Characterization of the lanthanum(III) and europium(III) trichloroacetate complexes extracted with 18-crown-6

    International Nuclear Information System (INIS)

    Imura, H.; Saito, Y.; Ohashi, K.; Meguro, Y.; Yoshida, Z.; Choppin, G.R.

    1996-01-01

    Extraction of lanthanide(III) ions with 18-crown-6 (18C6) and trichloroacetate (tca) has been studied. The composition, hydration, and structure of the La(III) and Eu(III) complexes extracted into 1,2-dichloroethane were investigated by using several methods such as the liquid-liquid distribution technique, conductimetry, Karl Fisher titration, laser luminescence spectroscopy, and 1 H NMR. The La(III) complex was found to be a monohydrate, La(tca) 3 (18C6)(H 2 O), while that of Eu(III) was a mixture of a monohydrate and a dihydrate, i.e., Eu(tca) 3 (18C6)(H 2 O) and Eu(tca) 3 (18C6)(H 2 O) 2 . The origin of the selectivity by 18C6 which gives much higher extractability of La(III) than of Eu(III) is explained by considering the hydration and probable structure of their complexes. 12 refs., 5 figs., 4 tabs

  20. Distribution of (14 C) photosynthates in 3 periods during the plant-cane cycle

    International Nuclear Information System (INIS)

    Pimentel, R.M.M.

    1989-04-01

    Plant-cane stools were labelled with 14 CO 2 in the field, at Goiana-PE, Brazil, when 3,7 and 11 months old. Each stool was enclosed in a chamber with 14 CO 2 for 90 minutes. The 14 C photosynthates were measured in leaves, stalks, roots and soil 1, 7, 15, 30, 60 and 90 days after labelling. Roots were divided into alive and dead and soil into rizosphere and outer soil. The soil was incubated for 10 days to measure C mineralization. At end of the labelling period at 3,7 and 11 months, 2, 19 and 1% of the initial 14 CO 2 were recovered in the plant and the soil. The low recovery of 14 C at 3 months could be attributed to losses by respiration and lack of sampling of the top growing point. The low CO 2 fixation and losses by respiration at first sampling in the 7 months old labelling were attributed to low light intensity during the day of labelling. In the following sampling, total 14 C recoveries varied little and there was little change in the proportion of 14 C in each part, indicating that the 14 C was already incorporated in stable organic fractions. Most of the recovered 14 C C>80%) was founded in the leaves but all plant parts received labelled photosynthates. (author)

  1. Turnover of 14C-glucose in soils and its relationship with soil characters

    International Nuclear Information System (INIS)

    Ni Jinzhi; Xu Jianmin; Xie Zhengmiao; Ye Qingfu

    2001-01-01

    The turnover of 14 C-glucose added in 13 soils was studied. The turnover rate of 14 C-glucose can be divided into three phases: 0 - 3d, 3 - 28d and 28 - 294d. The range of the turnover rate and half -life of 14 C-glucose were 1.3 x 10 -1 - 2.5 x 10 -1 d -1 and 3 - 5d, 0.7x 10 -2 - 1.2 x 10 -2 d -1 and 58 - 97d, 0.5 x 10 -3 - 1.4 x 10 -3 d -1 and 491 - 1504d, respectively. Correlation analysis showed that from 0 to 3 days the turnover rate of 14 C-glucose had significant positive correlation with soil qCO 2 , from 3 to 28 days, the turnover rate of 14 C-glucose had no significant correlation with soil physico-chemical and biological properties. The turnover rate of 14 C-glucose had significant or highly significant negative correlation with soil total organic carbon, total nitrogen, CEC and significant positive correlation with soil sand content during the period from 28 to 294 days. Turnover of 14 C-glucose during the third period has close correlation with soil properties

  2. Disposition of 14C-β-carotene following delivery with autologous triacylglyceride-rich lipoproteins

    International Nuclear Information System (INIS)

    Dueker, Stephen R.; Le Thuy Vuong; Faulkner, Brian; Buchholz, Bruce A.; Vogel, John S.

    2007-01-01

    Following ingestion, a fraction of β-carotene is cleaved into vitamin A in the intestine, while another is absorbed intact and distributed among tissues and organs. The extent to which this absorbed β-carotene serves as a source of vitamin A is unknown in vivo. In the present study we use the attomole sensitivity of accelerator mass spectrometry (AMS) for 14 C to quantify the disposition of 14 C-β-carotene (930 ng; 60.4 nCi of activity) after intravenous injection with an autologous triacylglyceride-rich lipoprotein fraction in a single volunteer. Total 14 C was quantified in serial plasma samples and also in triglyceride-rich, and low density lipoprotein, subfractions. The appearance of 14 C-retinol, the circulating form of vitamin A in plasma, was determined by chromatographic separation of plasma retinol extracts prior to AMS analysis. The data showed that 14 C concentrations rapidly decayed within the triglyceride-rich lipoprotein fractions after injection, whereas low density lipoprotein 14 C began a significant rise in 14 C 5 h post dose. Plasma 14 C-retinol also appeared at 5 h post dose and its concentrations were maintained above baseline for >88 days. Based upon comparisons of 14 C-retinol concentrations following an earlier study with orally dosed 14 C-β-carotene, a molar vitamin A value of the absorbed β-carotene of 0.19 was derived, meaning that 1 mole of absorbed β-carotene provides 0.19 moles of vitamin A. This is the first study to show that infused β-carotene contributes to the vitamin A economy in humans in vivo

  3. Synthesis of glycolic acid-1-14C of high specific activity

    International Nuclear Information System (INIS)

    Ramamurthy, T.V.; Viswanathan, K.V.

    1987-01-01

    A simple procedure is described which efficiently converts traces of 14 C labelled cyanide present as a dilute solution into glycolic acid-1- 14 C with more than 85% radiochemical recovery and of high specific activity. (author)

  4. Plasma kinetics of 14C-uric acid in bulls

    International Nuclear Information System (INIS)

    Cetinkaya, N.

    1999-01-01

    Plasma kinetics of uric acid were followed by 14C labelled uric acid to measure the effects of feed intake upon kinetic parameters. Two bulls (average L W 346±79 kg) were given an intravenous administration of a tracer (8-14C-uric acid, 250μCi/50 ml) by single injection via a jugular catheter. Animals were fed a mixed diet containing 30% wheat straw and 70% compounded feed as 95 and 60 % of the voluntary intake. Voluntary intakes were 8 kg/d as fed for two bulls. Blood samples, were collected at 0, 0.5,1, 2, 3, 4, 6, 8, 12, 16, 24 and 28 h after tracer administration. Fractional rates of clearance from the blood and pool size of compartments in the blood were estimated using plasma 8-14C-counts, following the method proposed by Chen and Franklin. The mean values of fractional rates (K 2,1 , K 1,2 ) and compartments pool size (V 1 , V 2 ) and the total pool size of compartments I and 2 at 60% and 95% feeding level were 1.97 and 1.44, 1.06 and 0.78; 76.9 L and 94.5 L, 137.01 L and 163.51 L; 214.0 L and 250.3 L respectively. Plasma kinetic parameters of 14C-uric acid were not affected at different feed intakes

  5. Identification of the receptors for somatostatin (SST) and cortistatin (CST) in chickens and investigation of the roles of cSST28, cSST14, and cCST14 in inhibiting cGHRH1-27NH2-induced growth hormone secretion in cultured chicken pituitary cells.

    Science.gov (United States)

    Meng, Fengyan; Huang, Guian; Gao, Shunyu; Li, Juan; Yan, Zhenxin; Wang, Yajun

    2014-03-25

    Somatostatin receptors (SSTRs) are proposed to mediate the actions of somatostatin (SST) and its related peptide, cortistatin (CST), in vertebrates. However, the identity, functionality, and tissue expression of these receptors remain largely unknown in most non-mammalian vertebrates including birds. In this study, five SSTRs (named cSSTR1, cSSTR2, cSSTR3, cSSTR4, cSSTR5) were cloned from chicken brain by RT-PCR. Using a pGL3-CRE-luciferase reporter system, we demonstrated that activation of each cSSTR expressed in CHO cells by cSST28, cSST14 and cCST14 treatment could inhibit forskolin-induced luciferase activity of CHO cells, indicating the functional coupling of all cSSTRs to Gi protein(s). Interestingly, cSSTR1-4 expressed in CHO cells could be activated by cSST28, cSST14 and cCST14 with high potencies, suggesting that they may function as the receptors common for these peptides. In contrast, cSSTR5 could be potently activated by cSST28 only, indicating that it is a cSST28-specific receptor. Using RT-PCR, wide expression of cSSTRs was detected in chicken tissues including pituitary. In accordance with their expression in pituitary, cSST28, cSST14, and cCST14 were demonstrated to inhibit basal and novel cGHRH1-27NH2-induced GH secretion in cultured chicken pituitary cells dose-dependently (0-10nM) by Western blot analysis, suggesting the involvement of cSSTR(s) common for these peptides in mediating their inhibitory actions. Collectively, our study establishes a molecular basis to elucidate the roles of SST/CST in birds and provide insights into the roles of SST/CST in vertebrates, such as their conserved actions on pituitary. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

  6. Diurnal productivity and apparent 14C-calcification in the staghorn coral, Acropora acuminata

    International Nuclear Information System (INIS)

    Barnes, D.J.; Crossland, C.J.

    1978-01-01

    The rate of 14 C-fixation by Acropora acuminata tissues showed a marked increase after dawn. However, maximum 14 C-fixation was not achieved until early afternoon. The apparent 14 C-incorporation rate into the skeleton of whole branches reached a peak around noon. However, the major period of 14 C-deposition occurred from noon to mid-afternoon. The broad peak of 14 C-incorporation into skeleton of whole branches reflects two rate maxima; a late-morning maximum of zooxanthellae-free terminal calices, probably related to translocation of fixed carbon from basal tissues; and an early afternoon maximum for the zooxanthellae-containing basal areas of branches. (author)

  7. Apportioning bacterial carbon source utilization in soil using 14 C isotope analysis of FISH-targeted bacterial populations sorted by fluorescence activated cell sorting (FACS): 14 C-FISH-FACS.

    Science.gov (United States)

    Gougoulias, Christos; Meade, Andrew; Shaw, Liz J

    2018-02-19

    An unresolved need in microbial ecology is methodology to enable quantitative analysis of in situ microbial substrate carbon use at the population level. Here, we evaluated if a novel combination of radiocarbon-labelled substrate tracing, fluorescence in situ hybridisation (FISH) and fluorescence-activated cell sorting (FACS) to sort the FISH-targeted population for quantification of incorporated radioactivity ( 14 C-FISH-FACS) can address this need. Our test scenario used FISH probe PSE1284 targeting Pseudomonas spp. (and some Burkholderia spp.) and salicylic acid added to rhizosphere soil. We examined salicylic acid- 14 C fate (mineralized, cell-incorporated, extractable and non-extractable) and mass balance (0-24 h) and show that the PSE1284 population captured ∼ 50% of the Nycodenz extracted biomass 14 C. Analysis of the taxonomic distribution of the salicylic acid biodegradation trait suggested that PSE1284 population success was not due to conservation of this trait but due to competitiveness for the added carbon. Adding 50KBq of 14 C sample -1 enabled detection of 14 C in the sorted population at ∼ 60-600 times background; a sensitivity which demonstrates potential extension to analysis of rarer/less active populations. Given its sensitivity and compatibility with obtaining a C mass balance, 14 C-FISH-FACS allows quantitative dissection of C flow within the microbial biomass that has hitherto not been achieved. © 2018 Society for Applied Microbiology and John Wiley & Sons Ltd.

  8. Defective (U-14 C) palmitic acid oxidation in Duchenne muscular dystrophy

    Energy Technology Data Exchange (ETDEWEB)

    Carroll, J.E.; Norris, B.J.; Brooke, M.H.

    1985-01-01

    Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased (U-14 C) palmitic acid oxidation. (1-14 C) palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation.

  9. Defective [U-14 C] palmitic acid oxidation in Duchenne muscular dystrophy

    International Nuclear Information System (INIS)

    Carroll, J.E.; Norris, B.J.; Brooke, M.H.

    1985-01-01

    Compared with normal skeletal muscle, muscle from patients with Duchenne dystrophy had decreased [U-14 C] palmitic acid oxidation. [1-14 C] palmitic acid oxidation was normal. These results may indicate a defect in intramitochondrial fatty acid oxidation

  10. Probable alpha and 14C cluster emission from hyper Ac nuclei

    International Nuclear Information System (INIS)

    Santhosh, K.P.

    2013-01-01

    A systematic study on the probability for the emission of 4 He and 14 C cluster from hyper Λ 207-234 Ac and non-strange normal 207-234 Ac nuclei are performed for the first time using our fission model, the Coulomb and proximity potential model (CPPM). The predicted half lives show that hyper Λ 207-234 Ac nuclei are unstable against 4 He emission and 14 C emission from hyper Λ 217-228 Ac are favorable for measurement. Our study also show that hyper Λ 207-234 Ac are stable against hyper Λ 4 He and Λ 14 C emission. The role of neutron shell closure (N = 126) in hyper Λ 214 Fr daughter and role of proton/neutron shell closure (Z ∼ 82, N = 126) in hyper Λ 210 Bi daughter are also revealed. As hyper-nuclei decays to normal nuclei by mesonic/non-mesonic decay and since most of the predicted half lives for 4 He and 14 C emission from normal Ac nuclei are favourable for measurement, we presume that alpha and 14 C cluster emission from hyper Ac nuclei can be detected in laboratory in a cascade (two-step) process. (orig.)

  11. Uptake and release of [14C] GABA from rabbit retina synaptosomes

    International Nuclear Information System (INIS)

    Redburn, D.A.

    1977-01-01

    A partial separation of two synaptosomal fractions was achieved using modifications of conventional homogenization and centrifugation techniques. The two fractions contained morphologically distinct synaptosomal populations, receptor cell synaptosomes (large synaptosomes, P 1 ), and synaptosomes from the other cell types (smaller, conventional-sized synaptosomes, P 2 ). [ 14 C]GABA was bound and released from subcellular fractions from retina under conditions which support its role as a neurotransmitter in retina. On the other hand, [ 3 H]leucine, which is very likely a non-transmitter compound, was bound by retinal fractions but not released to the appropriate stimulation. [ 14 C]GABA binding and release sites were more prevalent in P 2 fractions. [ 14 C]GABA was bound by P 1 fractions containing photoreceptor synaptosomes; however, the K + stimulated release of [ 14 C]GABA appeared to be insensitive to external Ca 2+ . Possible mechanisms are discussed. (author)

  12. Absorption, distribution, and metabolism of [14C]chlorpyrifos applied dermally to goats

    International Nuclear Information System (INIS)

    Cheng, T.; Bodden, R.M.; Puhl, R.J.; Bauriedel, W.R.

    1989-01-01

    Radiolabeled chlorpyrifos [O,O-diethyl O-(3,5,6-trichloro-2-pyridyl) phosphorothioate] was applied dermally to two male weanling goats, at a dose of 22 mg/kg of body weight. A blood sample was drawn before dosing and every 4 h thereafter. The animals were sacrificed approximately 18 h after dosing, when blood radioactivity levels at 16 h had declined from maximum values (12 h) in both animals. Radioanalysis of blood and selected tissues (liver, kidney, heart, fat, muscle) indicated that radioactivity levels were, in general, very low, ranging from 0.04 ppm (chlorpyrifos equivalents) in muscle to 0.90 ppm in omental fat. Tissue extracts contained 80-96% of the 14 C residue, most of which was organosoluble. High-performance liquid chromatography analysis of tissue extracts showed that the predominant 14 C residue in liver and kidney was [ 14 C]-3,5,6-trichloro-2-pyridinol (chlorpyridinol) whereas [ 14 C]chlorpyrifos was predominant in fat and heart extracts. In muscle, in addition to approximately equal amounts of [ 14 C]chlorpyridinol and [ 14 C]chlorpyrifos, 18.6% of the radioactivity was unidentified; alkaline hydrolysis quantitatively converted the latter radioactivity to pyridinol

  13. Preparation of saccharides uniformly labelled with 14C radioisotope. Part VI

    International Nuclear Information System (INIS)

    Skala, L.

    1987-01-01

    1,6-anhydro-β-D-[U- 14 C]-glucopyranose was prepared by pyrolysis of U- 14 C-glucane from the Chlorella vulgaris Beijerinck algae at reduced pressure. The compound was separated by preparative paper chromatography with yields of 25 to 30% relative to the radioactivity of the initial[U- 14 C]glucane. The compound whose preparation has not been described in the literature is of a potential value as an initial compound for the preparation of a number of saccharides and their derivatives that are difficult to obtain. (author). 1 fig., 20 refs

  14. Studies on the cytotoxicity and anticancer performance of heterocyclic hypervalent organobismuth(III) compounds.

    Science.gov (United States)

    Liu, Yong-Ping; Lei, Jian; Tang, Li-Wen; Peng, Yao; Au, Chak-Tong; Chen, Yi; Yin, Shuang-Feng

    2017-10-20

    Novel organobismuth(III) complex of 5H-dibenzo[c,f][1,5]oxabismocin-12(7H)-yl nitrate (C2) was synthesized and characterized by spectral and elemental analysis. It was compared with other five C,E,C-chelating (E = N, O, S) organobismuth(III) complexes against human adenocarcinoma alveolar basal epithelial cells (A549), human liver cancer cell line (SMCC7721), human gastric cancer cell line (SGC-7901), human colon adenocarcinoma cell line (SW480) and healthy human bronchial cell line (16HBE14o-) in vitro. It was found that C2 exhibited the best anticancer activity. Further mechanistic investigation indicated that toxicological activity of C2 was ascribable to apoptosis rather than anti-proliferative activity. Apoptosis was induced through up-regulating the level of Bcl-2/Bax as well as the activation of caspase-3. The results demonstrate that heterocyclic organobismuth(III) complexes of this type have great potential in the treatment of cancer. Copyright © 2017 Elsevier Masson SAS. All rights reserved.

  15. Elimination of the 12 C and 16 O in the elastic scattering of 14 C by polarized protons

    International Nuclear Information System (INIS)

    Avila A, O.L.; Ramirez T, J.J.; Murillo O, G.; Fernandez B, M.

    1991-04-01

    The study of the elastic scattering of 14 C for polarized protons it provides information on the nuclear structure of 15 N. In the Tandem accelerator of the Nuclear Center in collaboration with the University of Notre Dame is carrying out this study to energy between 5.0 and 9.0 MeV in steps of 10 keV. The measures of differential section and vectorial analyzer power are subjected to shift analysis of phase being able to determine the parameters of the excited levels of 15 N that are it angular momentum, parity, level width and elastic width. The details of this experiment are presented in the ACEL-9102 technical report while in this work it was discussed the way in that contributions of 12 C and 16 O are eliminated that are present as impurities in our target of 14 C. At small angles the elastic components of these impurities are shoveled with the elastic of 14 C. In the experiment carried out in the Nuclear Center were take measures of differential section for 6 angles; 35, 45, 55, 65, 145 and 165 using surface barrier detectors. It is observed that it exists shovels at 35, 45, 55 and 65 while at 145 and 165 the 12 C, the 14 C and the 16 O are totally separate. With the purpose of being able to subtract of the elastic of 14 C the proportion of 12 C, it was decided to bombard a target of 12 C leaving the same geometry that had been used to bombard 14 C. With this also carried out the reaction 12 C (p,p) 12 C between 5.0 and 9.0 MeV in steps of 50 keV. Starting from these spectra are the integration (yield) of the elastic of 12 C. (Author)

  16. Analysis of 14C and 13C in teeth provides precise birth dating and clues to geographical origin.

    Science.gov (United States)

    Alkass, K; Buchholz, B A; Druid, H; Spalding, K L

    2011-06-15

    The identification of human bodies in situations when there are no clues as to the person's identity from circumstantial data, poses a difficult problem to the investigators. The determination of age and sex of the body can be crucial in order to limit the search to individuals that are a possible match. We analyzed the proportion of bomb pulse derived carbon-14 ((14)C) incorporated in the enamel of teeth from individuals from different geographical locations. The 'bomb pulse' refers to a significant increase in (14)C levels in the atmosphere caused by above ground test detonations of nuclear weapons during the cold war (1955-1963). By comparing (14)C levels in enamel with (14)C atmospheric levels systematically recorded over time, high precision birth dating of modern biological material is possible. Above ground nuclear bomb testing was largely restricted to a couple of locations in the northern hemisphere, producing differences in atmospheric (14)C levels at various geographical regions, particularly in the early phase. Therefore, we examined the precision of (14)C birth dating of enamel as a function of time of formation and geographical location. We also investigated the use of the stable isotope (13)C as an indicator of geographical origin of an individual. Dental enamel was isolated from 95 teeth extracted from 84 individuals to study the precision of the (14)C method along the bomb spike. For teeth formed before 1955 (N=17), all but one tooth showed negative Δ(14)C values. Analysis of enamel from teeth formed during the rising part of the bomb-spike (1955-1963, N=12) and after the peak (>1963, N=66) resulted in an average absolute date of birth estimation error of 1.9±1.4 and 1.3±1.0 years, respectively. Geographical location of an individual had no adverse effect on the precision of year of birth estimation using radiocarbon dating. In 46 teeth, measurement of (13)C was also performed. Scandinavian teeth showed a substantially greater depression in

  17. 13C/14C dual isotope breath test measurement of gastric emptying in normal subjects and patients

    International Nuclear Information System (INIS)

    Chew, G.; Bartholomeusz, F.D.L.; Bellon, M.; Chatterton, B.E.

    2000-01-01

    Full text: A more flexible alternative to dual isotope scintigraphy for gastric emptying involves measuring breath C0 2 after administration of absorbable tracers. Method: six patients were given 100g hamburger labelled with 25 MBq 99 Tc m sulphur colloid and 74 KBq 14 C octanoic acid, and 150 ml 10% glucose drink labelled with 8 MBq 67 Ga citrate and ISO mg 13 C acetate and seven normals with 14 C and 13 C labels only. Breath was collected at baseline and then regularly for four hours. The 14 CO 2 and 13 CO 2 activity was measured with liquid scintillation counting and mass spectroscopy. The times to maximum 14 CO 2 , and 13 CO 2 , T max, were determined. Results: Comparison was made between 14 CO 2 T max with scintigraphic retention of 99 Tc m at 100 minutes (SR100m) and 13 CO 2 T max with the scintigraphic half-clearance time of 67 Ga (scint T1/2). In conclusion 14 CO 2 T max and 13 CO 2 T max correlate significantly with SR100m and scint T1/2 respectively. The normal threshold is between 165 and 180 minutes for 14 Co 2 T max; probably > 40 minutes for 13 CO 2 T max but overlap exists between normal and abnormal results in this small preliminary study. Recruitment is to continue to better define normal ranges. Copyright (2000) The Australian and New Zealand Society of Nuclear Medicine Inc

  18. Radiocarbon (14C) Concentration of Local Pollution in Street Trees Located at Intersections

    OpenAIRE

    Ogawa, Daisuke

    2018-01-01

    At large intersections, vehicles consume and generate a large amount of fossil fuel. Carbon derived from fossil fuels that do not contain radioactive carbon (14C), i.e., dead carbon, is released in large amounts in the roadside air environment. By means of photosynthesis, street trees along the roadside assimilate both dead carbon, not containing radioactive carbon (14C), and contemporary carbon, which includes radioactive carbon (14C). Therefore, the concentration of radioactive carbon (14C)...

  19. Comparison of Accuracy Between 13C- and 14C-Urea Breath Testing: Is an Indeterminate-Results Category Still Needed?

    Science.gov (United States)

    Charest, Mathieu; Bélair, Marc-André

    2017-06-01

    Helicobacter pylori infection is the leading cause of peptic ulcer disease. The purpose of this study was, first, to assess the difference in the distribution of negative versus positive results between the older 14 C-urea breath test and the newer 13 C-urea breath test and, second, to determine whether use of an indeterminate-results category is still meaningful and what type of results should trigger repeated testing. Methods: A retrospective survey was performed of all consecutive patients referred to our service for urea breath testing. We analyzed 562 patients who had undergone testing with 14 C-urea and 454 patients who had undergone testing with 13 C-urea. Results: In comparison with the wide distribution of negative 14 C results, negative 13 C results were distributed farther from the cutoff and were grouped more tightly around the mean negative value. Distribution analysis of the negative results for 13 C testing, compared with those for 14 C testing, revealed a statistically significant difference between the two. Within the 13 C group, only 1 patient could have been classified as having indeterminate results using the same indeterminate zone as was used for the 14 C group. This is significantly less frequent than what was found for the 14 C group. Discussion: Borderline-negative results do occur with 13 C-urea breath testing, although less frequently than with 14 C-urea breath testing, and we will be carefully monitoring differences falling between 3.0 and 3.5 %Δ. 13 C-urea breath testing is safe and simple for the patient and, in most cases, provides clearer positive or negative results for the clinician. © 2017 by the Society of Nuclear Medicine and Molecular Imaging.

  20. Persistence of 14C maneb in lettuce plants an soil

    International Nuclear Information System (INIS)

    Bennaceur, M.; Sennaoui, Z.; Meguenni, H.

    1992-10-01

    Maneb residue is studied on lettuce plant and soil after spraying on greenhouse with 14C maneb. The residues declined with time. After 37 days from the application, 14C maneb residues in water extracts declined to 1,5. 10-2ug/g from 5,8. 10-1ug/g of the zero day sample in lettuce plants and 4,6. 10-3ug/g from 1,73. 10-1ug/g in soil. The 14C internals residues in lettuce and soil increase respectively till 16 days and 24 days, then decrease to 88% and 4,05% after 37 days. ETU was present in lettuce plant after 8 days then decreases with time. Two metabolites were identified by TLC (EU,ETU)

  1. Synthesis of 7-[α-(2-amino-[2-14C]thiazol-4-yl)-α-(Z)-methoxyimin oacetamido]-3-(1-methylpyrrolidinio)methyl-3-cephem-4-carboxylate hydrochloride ([14C]cefepime hydrochloride)

    International Nuclear Information System (INIS)

    Standridge, R.T.; Swigor, J.E.

    1993-01-01

    The title compound ([ 14 C]cefepime hydrochloride) was prepared as follows:- [ 14 C]Thiourea was condensed with ethyl 4-bromo-3-oxo-2-methoxyimino-acetate providing ethyl 2-(2-amino-4-[2- 14 C] thiazolyl)-2-methoxyi-minoacetate as the pure Z-isomer. Saponification gave the amino acid this was reacted with 1-hydroxybenzotriazole to give the activated ester. Condensation in situ with 7-amino-3-(1-methylpyrrolidinio) methyl-3-cephem-4-carboxylate yielded the product as the pure sulfate salt. Treatment of the sulfate salt with base provided the zwitterion isolated as the stable N-methyl-2-pyrrolidinone adduct. An aqueous solution of the adduct was converted to the crystalline title compound, [ 14 C]Cefepime hydrochloride hydrate, with hydrochloric acid/acetone. Radiochemical purity was 99.0% and specific activity, 34.2 μCi/mg. Overall yield from [ 14 C]thiourea was 18%. (Author)

  2. Detection of 14C in natural trace organics recovered from groundwater

    International Nuclear Information System (INIS)

    Murphy, E.; Long, A.; Davis, S.N.; Donahue, D.

    1985-01-01

    Radiocarbon measurements on dissolved inorganic carbon (DIC) in groundwater have given the authors insight into chemical and hydrological processes occurring in aquifers. Carbon-14 analyses on various dissolved organic carbon (DOC) fractions from groundwater are only starting, but, as is true for DIC 14 C measurements, their significance reaches beyond dating of water and into chemical processes in the aquifer and recharge zone. When combined with information on the chemical character of the DOC, 14 C data may clarify the origin and diagenesis of organic carbon in groundwater. In the past, research into the 14 C has been discouraged by the low concentrations of DOC in groundwater, typically in the μg/l range. The tandem accelerator at the University of Arizona can analyze 14 C in as little as 1 mg of carbon, thus requiring isolation of the DOC from 200 l or less of groundwater. This paper describes the techniques bring used for separation of the DOC in groundwater, some of the data collected, and the significance of these data

  3. Synthesis and analysis of the opioid analgesic [[sup 14]C]-fentanyl

    Energy Technology Data Exchange (ETDEWEB)

    Bagley, J.R.; Wilhelm, J.A. (Anaquest Inc., Murray Hill, NJ (United States))

    1992-11-01

    The synthesis of [[sup 14]C]-fentanyl, the radiolabelled congener of the potent opioid analgesic chosen for utilization in drug disposition studies, is described. [[sup 14]C]-Labelling was achieved in the first of two steps, a room temperature reduction of the in situ generated Schiff base from 1-phenylethyl-4-piperidone and [UL-[sup 14]C]-aniline hydrochloride with sodium triacetoxyborohydride. A nearly instantaneous production of fentanyl was accomplished at room temperature with the addition of propionyl chloride. The overall radiochemical yield was 18%. The method described is efficiently adaptable for submicromolar scale while yielding a product of sufficient specific activity for in vivo studies. Our solvent system for thin layer chromatography was superior to the USP system reported for chromatographic analysis of fentanyl. This is the first reported preparation of [[sup 14]C]-fentanyl with the radiolabel in the aniline benzene ring. (author).

  4. Inner-sphere and outer-sphere complexes of yttrium(III), lanthanum (III), neodymium(III), terbium(III) and thulium(III) with halide ions in N,N-dimethylformamide

    International Nuclear Information System (INIS)

    Takahashi, Ryouta; Ishiguro, Shin-ichi

    1991-01-01

    The formation of chloro, bromo and iodo complexes of yttrium(III), and bromo and iodo complexes of lanthanum(III), neodymium(III), terbium(III) and thulium(III) has been studied by precise titration calorimetry in N,N-dimethylformamide (DMF) at 25 o C. The formation of [YCl] 2+ , [YCl 2 ] + , [YCl 3 ] and [YCl 4 ] - , and [MBr] 2+ and [MBr 2 ] + (M = Y, La, Nd, Tb, Tm) was revealed, and their formation constants, enthalpies and entropies were determined. It is found that the formation enthalpies change in the sequence ΔH o (Cl) > ΔH o (l), which is unusual for hard metal (III) ions. This implies that, unlike the chloride ion, the bromide ion forms outer-sphere complexes with the lanthanide(III) and yttrium(III) ions in DMF. Evidence for either an inner- or outer-sphere complex was obtained from 89 Y NMR spectra for Y(ClO 4 ) 3 , YCl 3 and YBr 3 DMF solutions at room temperature. (author)

  5. Preparation of 14C-labelled urea for diagnosis of helicobacter pylori infection

    International Nuclear Information System (INIS)

    Jiang Bingsheng

    2001-01-01

    The preparation of 14 C-urea from [ 14 C]-barium carbonate is reported. The results show that chemical yield can reach 80% (average of 6 runs); melt point is 132 - 136 degree C; purity is 99.65% - 99.85%. After being analyzed by IR, UV, NMR, MS, and elemental analysis, the 14 C-urea has the same molecular structure as that of standard urea. Animal trial indicates that clinical use is safe. Good stability is shown by stability testing under different luminous flux, temperature and relative humidity

  6. Fate and bioavailability of 14C-pyrene and 14C-lindane in sterile natural and artificial soils and the influence of aging

    International Nuclear Information System (INIS)

    Šmídová, Klára; Hofman, Jakub; Ite, Aniefiok E.; Semple, Kirk T.

    2012-01-01

    Soil organic matter is used to extrapolate the toxicity and bioavailability of organic pollutants between different soils. However, it has been shown that other factors such as microbial activity are crucial. The aim of this study was to investigate if sterilization can reduce differences in the fate and bioavailability of organic pollutants between different soils. Three natural soils with increasing total organic carbon (TOC) content were collected and three artificial soils were prepared to obtain similar TOCs. Soils were sterilized and spiked with 14 C-pyrene and 14 C-lindane. Total 14 C radioactivity, HPCD extractability, and bioaccumulation in Eisenia fetida were measured over 56 days. When compared to non-sterile soils, differences between the natural and artificial soils and the influence of soil-contaminant contact time were generally reduced in the sterile soils (especially with middle TOC). The results indicate the possibility of using sterile soils as “the worst case scenario” in soil ecotoxicity studies. - Highlights: ► Sterile artificial and natural soils with the same TOC content were used. ► The fate and behavior of two 14 C-POPs were studied over 56 days after spiking. ► Sterilization reduced differences between artificial and natural soils. ► There was no effect of time (aging) in POPs bioaccumulation. ► Sterile soils may be used as “the worst case scenario” in POPs availability studies. - Sterilization reduced the differences in POPs fate and bioavailability between artificial and natural soils with the same TOC content and eliminated the influence of soil contact time.

  7. Concentration and distribution of 14C in aquatic environment around Qinshan nuclear power plant

    International Nuclear Information System (INIS)

    Wang Zhongtang; Guo Qiuju; Hu Dan; Xu Hong

    2015-01-01

    In order to study the concentration and distribution of 14 C in aquatic environment in the vicinity of Qinshan Nuclear Power Plant (NPP) after twenty years' operation, an apparatus extracting dissolved inorganic carbon from water was set up and applied to pretreat the water samples collected around Qinshan NPP. The 14 C concentration was measured by accelerator mass spectrometer (AMS). The results show that the 14 C specific activities in surface seawater samples range from 196.8 to 206.5 Bq/kg 203.4 ± 5.6) Bq/kg in average), which are close to the background. The 14 C concentrations in cooling water discharged from Qinshan NPP are close to the 14 C values in near shore seawater samples out of liquid radioactive effluent discharge period. It can be further concluded that the 14 C discharged previously is diluted and diffused well, and no 14 C enrichment in seawater is found. Also, no obvious increment in the 14 C specific activities of surface water and underground water samples are found between Qinshan NPP region and the reference region. (authors)

  8. Fate of [14C]-zineb on lettuce plants

    International Nuclear Information System (INIS)

    Vonk, J.W.

    1976-01-01

    [1,2- 14 C]-zinc ethylenebisdithiocarbamate (zineb) was prepared and applied in droplets to leaves of lettuce plants. In aqueous suspension zineb decomposes mainly into ethylenethiourea (ETU) and 5,6-dihydro-3H-imidazo[2,1-C]-1,2,4-dithiazole-3-thione (DIDT). Lettuce plants were harvested 0,1,3,7,14 and 21 days after treatment and analysed. A high proportion of radioactivity remained on the surface of the plant and could be washed off. The following identified products were present: unchanged zineb, ETU, DIDT, 2-imidazoline and ethyleneurea. The ETU residue disappeared within 7 days, while 2-imidazoline and ethyleneurea were formed gradually. Radioactivity inside the plant consisted mostly of ethyleneurea: no ETU was present. (author)

  9. Complete fusion of the 12C+12O, 14N+12C and 15N+12C systems

    International Nuclear Information System (INIS)

    Conjeaud, M.; Gary, S.; Harar, S.; Wieleczko, J.P.

    1978-01-01

    Cross sections for evaporation residues following the complete fusion of the 12 C+ 12 C, 14 N+ 12 C and 15 N+ 12 C systems have been measured with a E-ΔE counter telescope in a wide range of incident energies. They are fairly well reproduced by evaporation calculations based on the statistical theory. The total fusion excitation function of the 12 C+ 12 C system shows strong structure, which is compared to the predictions of the reaction cross sections derived from coupled channel calculations and to the integrated inelastic cross sections. Critical angular momenta have been obtained from the fusion cross-section data and these values are discussed in the framework of compound nucleus and entrance channel effects. A striking difference is observed between the fusion cross sections of the 14 N+ 12 C and 15 N+ 12 C systems and shows the importance of the valence nucleons of colliding ions in the fusion process. A possible interpretation might be the influence of the yrast line of the compound nuclei. (Auth.)

  10. IgE and IgG cross-reactivity among Lol p I and Lol p II/III. Identification of the C-termini of Lol p I, II, and III as cross-reactive structures

    NARCIS (Netherlands)

    van Ree, R.; van Leeuwen, W. A.; van den Berg, M.; Weller, H. H.; Aalberse, R. C.

    1994-01-01

    In this study, the homologous C-termini of Lol p I, Lol p II, and Lol p III were shown to contain cross-reactive B-cell epitopes. This was demonstrated by inhibition studies with purified Lol p I, II, and III and synthetic peptides of their C-termini. It was ruled out that the observed

  11. Synthesis of /sup 14/C-cysteamine and cystamine

    Energy Technology Data Exchange (ETDEWEB)

    Pantev, T

    1975-01-01

    The compound 2-mercapto-ethylamine-1,2 C/sup 14/ (cysteamine) was synthesized by adding 430 mg (10 mM) ethylimine-C/sup 14/ (specific activity of 500 microcuries per mmol) to 100 ml of absolute ethyl alcohol cooled to 0/sup 0/C in a 300 ml Erlenmeyer flask. A rapid flow of dry hydrogen sulfide was passed through this solution for two hours which then was allowed to stand for 20 hours additional under pressure. Dry argon is used to degas and to evaporate the solution. The yield is 480 mg (62 percent) of cysteamine with a specific activity of 400 microcuries per mmol. The salicylate derivative of cysteamine was isolated by crystallizing 460 mg of cysteamine C/sup 14/ dissolved in 20 ml of absolute ethyl alcohol with 840 mg of salicylic acid. The cysteamine hydrochloride compound was obtained by dissolving 100 mg of the cysteamine salicylate in 5 ml of water, acidifying with concentrated hydrochloric acid to a pH of 1 to 2, and extracting with 5 ml of ether five times. Yield is 90 percent. Cystamine was obtained by dissolving 100 mg of cysteamine hydrochloride in 20 ml of 50 percent ethyl alcohol, titrating with a 0.1 N solution of iodine in potassium iodide, adjusting with 0.1 N caustic to a pH of 10, and extracting with 5 ml of ether ten times. The compound purity is 95 percent with a 60 percent yield. 9 refs.

  12. Study on transference of assimilate in filling summer maize using isotope 14C

    International Nuclear Information System (INIS)

    Fan Zhongxue; Wang Pu; Liang Zhenxing

    2001-01-01

    The dynamic of assimilate transference from the ear leaf to grain during effective grain filling stage was studied by 14 C tracer. The results showed that the rates of assimilate transportation out of the ear leaf and transference to grain changed very fast. The rate was very big in 4 - 6 hour just after 14 C feeding and decreased with time. The grain which accumulated 14 C-assimilate in a higher rate and got much more 14 C-assimilate in fixed time could develop into larger size

  13. Carbon-14 isotope effects in the addition of 2,4-dinitrobenzenesulfenyl chloride to styrene-1-14C and styrene-2-14C

    International Nuclear Information System (INIS)

    Kanska, M.; Fry, A.

    1982-01-01

    The carbon-isotope effect reported here represents the first step in a general study of the mechanisms of simple electrophilic addition reactions by isotope effect techniques using the successive labeling approach. The addition of 2,4-dinitrobenzenesulfenyl chloride to styrene was chosen as a ''calibration case'' for the cyclic mechanism. The observed isotope effects at /sup α/C and /sup #betta#/C are fully consistent with the cyclic mechanism and probably inconsistent with the open carbenium ion mechanisms. The values of 12 k/ 14 k indicated in this report are averages (and standard deviations) of values for five different fractions of reaction ranging from 20% to 70% with the calculations being made by all four of the Tong and Yankwich equations for each fraction of reaction. Results indicated that there were no trends in the 12 k/ 14 k values as the fraction of reaction varied, and as can be seen by the low standard deviations, there was good agreement among the values calculated by the four equations. These two facts to indicate that the starting materials were of high chemical and radiochemical purity and that the procedures used in the isotope effect experiments were accurate and properly controlled

  14. The synthesis of [14C] C I pigment violet 19

    International Nuclear Information System (INIS)

    Filer, C.N.; Kelly, T.P.

    1990-01-01

    For the custom synthesis of radiolabeled compounds in the authors laboratory, aside from spectroscopic examination, their identity and radiochemical purity is routinely corroborated by demonstration of cochromatography with an authentic cold standard. In the synthesis of [ 14 C] red pigment 1 for the Cosmetic Toiletry and Fragrance Association, its insolubility precluded this. The preparation as well as characterization of 1 is described

  15. Cobalt Ion Promoted Redox Cascade: A Route to Spiro Oxazine-Oxazepine Derivatives and a Dinuclear Cobalt(III) Complex of an N-(1,4-Naphthoquinone)-o-aminophenol Derivative.

    Science.gov (United States)

    Mondal, Sandip; Bera, Sachinath; Maity, Suvendu; Ghosh, Prasanta

    2017-11-06

    The study discloses that the redox activity of N-(1,4-naphthoquinone)-o-aminophenol derivatives (L R H 2 ) containing a (phenol)-NH-(1,4-naphthoquinone) fragment is notably different from that of a (phenol)-NH-(phenol) precursor. The former is a platform for a redox cascade. L R H 2 is redox noninnocent and exists in Cat-N-(1,4-naphthoquinone)(2-) (L R 2- ) and SQ-N-(1,4-naphthoquinone) (L R •- ) states in the complexes. Reactions of L R H 2 with cobalt(II) salts in MeOH in air promote a cascade affording spiro oxazine-oxazepine derivatives ( OX L R ) in good yields, when R = H, Me, t Bu. Spiro oxazine-oxazepine derivatives are bioactive, and such a molecule has so far not been isolated by a schematic route. In this context this cascade is significant. Dimerization of L R H 2 → OX L R in MeOH is a (6H + + 6e) oxidation reaction and is composed of formations of four covalent bonds and 6-exo-trig and 7-endo-trig cyclization based on C-O coupling reactions, where MeOH is the source of a proton and the ester function. It was established that the active cascade precursor is [(L Me •- )Co III Cl 2 ] (A). Notably, formation of a spiro derivative was not detected in CH 3 CN and the reaction ends up furnishing A. The route of the reaction is tunable by R, when R = NO 2 , it is a (2e + 4H + ) oxidation reaction affording a dinuclear L R 2- complex of cobalt(III) of the type [(L NO2 2- ) 2 Co III 2 (OMe) 2 (H 2 O) 2 ] (1) in good yields. No cascade occurs with zinc(II) ion even in MeOH and produces a L Me •- complex of type [(L Me •- )Zn II Cl 2 ] (2). The intermediate A and 2 exhibit strong EPR signals at g = 2.008 and 1.999, confrming the existence of L Me •- coordinated to low-spin cobalt(III) and zinc(II) ions. The intermediates of L R H 2 → OX L R conversion were analyzed by ESI mass spectrometry. The molecular geometries of OX L R and 1 were confirmed by X-ray crystallography, and the spectral features were elucidated by TD DFT calculations.

  16. Articulación de fones en individuos clase esqueletal I,II y III Speech patterns in skeletal class I, II and III subjects

    Directory of Open Access Journals (Sweden)

    Pía Villanueva

    2009-09-01

    Full Text Available OBJETIVO: determinar los patrones de articulación de fones consonánticos en sujetos de habla española chilena clases I, II y III esqueletal; comparar las diferencias fonéticas que existan entre clases esqueletales. MÉTODOS: se seleccionaron 54 individuos que cumplían con los criterios de inclusión determinados mediante un examen clínico intraoral y a través del análisis de Ricketts, y se conformaron los grupos de estudio de pacientes clases esqueletales I, II y III. Se les realizó un examen fonoarticulatorio estandarizado para determinar los fones modificados y el patrón articulatorio compensatorio realizado. RESULTADOS: se observaron cambios en el punto de articulación de fones consonánticos en las tres clases esqueletales, con diferencias significativas en los grupos de fones anteriores y medios entre pacientes clases I y II, sólo en el grupo de los fones anteriores entre pacientes I y III. Entre pacientes clases II y III no se observaron diferencias significativas. Se reportan modificaciones y compensaciones cualitativamente distintas entre las clases esqueletales. CONCLUSIONES: en relación a pacientes clase I, los pacientes clase II o III, presentan distinto grado de modificación en el punto de articulación de fones consonánticos. Las diferencias observadas se relacionan con los patrones esqueletales propios de cada clase.PURPOSE: to determine the consonant phonemes articulation patterns in Chilean skeletal class I, II and III Spanish speakers and compare their phonetic differences. METHODS: fifty-four skeletal class I, II and III subjects were selected, based on intraoral clinical examination and Ricketts cephalometric analysis, constituting the study groups. A standardized phonoarticulatory test was applied to each patient to determine the modified phonemes and their compensatory patterns. RESULTS: the findings indicate changes in articulation in all three groups. Significant differences were found in anterior and medium

  17. 26 CFR 1.381(c)(14)-1 - Dividend carryover to personal holding company.

    Science.gov (United States)

    2010-04-01

    ... 26 Internal Revenue 4 2010-04-01 2010-04-01 false Dividend carryover to personal holding company. 1.381(c)(14)-1 Section 1.381(c)(14)-1 Internal Revenue INTERNAL REVENUE SERVICE, DEPARTMENT OF THE TREASURY (CONTINUED) INCOME TAX (CONTINUED) INCOME TAXES Insolvency Reorganizations § 1.381(c)(14)-1...

  18. Distribution and utilization of 14C-labelled assimilate in debranched soybeans

    International Nuclear Information System (INIS)

    Kokubun, Makie; Asahi, Yukimitsu

    1985-01-01

    Effects of debranching of soybean plants on the distribution and utilization of 14 C assimilate were studied. Leaves at different positions in the canopy were allowed to assimilate 14 CO 2 either at early flowering, at early pod growth, or at early pod-filling stage. Radioactivity at 24 hours or 7 days after labelling was measured in the component parts. Debranching increased the dry weight of the main stem resulting from greater increase at the lower section of the stem. The debranched plants had the leaves of higher assimilatory efficiency and delayed senescence. The leaves at lower position of the debranched plants exported 14 C less at flowering but more at early pod growth than those of controls. When 14 C was incorporated from upper leaves, the difference in the distribution pattern between the debranched and control plants was little. A greater portion of 14 C assimilate fixed at the lower leaves of the debranched plants was present at pods and stem + petioles of the lower section, in contrast to those of controls which exported some of the assimilate to the branches. Lower leaves of the debranched plants remained active even during pod growth stage, and a part of the fixed 14 C was translocated slowly into the root. The pattern of distribution and utilization of assimilate in debranched soybeans may account for the adaptability of the main stem type to higher planting density. (author)

  19. trans-(2-Benzoylpyridine-κ2N,Odichlorido[2-(2-pyridylcarbonylphenyl-κ2C1,N]iridium(III dichloromethane solvate

    Directory of Open Access Journals (Sweden)

    2009-03-01

    Full Text Available The title compound, [Ir(C12H8NOCl2(C12H9NO]·CH2Cl2, which was obtained from the reaction of iridium(III chloride trihydrate and 2-benzoylpyridine, contains an IrIII atom coordinated by two N, one O, one C and two Cl atoms in trans positions, forming a distorted octahedral environment. The solvent molecule CH2Cl2 is disordered over two positions with an occupancy of 0.8:0.2.

  20. 13C and 14C measurements on lake sediments of the Grosser Ploener See

    International Nuclear Information System (INIS)

    Erlenkeuser, H.; Willkomm, H.

    1979-01-01

    Radiocarbon age and 13 C content of organic and inorganic carbon fractions were measured for two sediment cores from the Grosser Ploener See (N-Germany), comprising the whole post-glacial. As compared to the age of the pollen stages, the 14 C age of the organic fraction is seen to show a hard-water effect of about 1000 years throughout the sediment column, indicating a constant recent activity of the lake bicarbonate of about 92% of the standard recent activity during the history of the lake. From the age of sediment samples corrected for hard water effect and for 14 C variations of the atmosphere the sedimentation rate is found to increase from 0.4 to 0.8 mm/year in the pre-Christian era to as high as 10 mm/year during the last 7 centuries. In the lower layers of the sediment, the 14 C content of the marl fraction corresponds to that of the organic component, indicating the autochthonous origin of these carbonates. During the last 2 1 /2 millenia, however, its 14 C content is too small by 10 to 30%, probably reflecting an allochthonous admixture. Increasing rate of sedimentation along with the growing accumulation of allochthonous minerals probably reflect the agricultural activity of man. It is associated with an increasing supply of nutrients to the lake particularly since a man-made rise of the water level at A.D. 1256, resulting in an enhanced rate of primary production which could be recognized from the stable carbon isotope ratios of both the sedimentary organic carbon and carbonate fraction. According to these results, the contribution of planktogenic organic matter to the sediments as compared to the supply of plant litter from the litoral zones is steadily increasing during the history of the lake and becomes the dominating part since the lake level risc in the Middle Ages. According to the 13 C/ 12 C-ratios, the carbonates of the sediment appear to have been precipitated preferentially in the litoral zones. (orig./MG) [de

  1. (CH4)-C-14 Measurements in Greenland Ice: Investigating Last Glacial Termination CH4 Sources

    DEFF Research Database (Denmark)

    Petrenko, V. V.; Smith, A. M.; Brook, E. J.

    2009-01-01

    by direct cosmogenic C-14 production in ice. C-14 of CO was measured to better understand this process and correct the sample (CH4)-C-14. Corrected results suggest that wetland sources were likely responsible for the majority of the Younger Dryas-Preboreal CH4 rise.......The cause of a large increase of atmospheric methane concentration during the Younger Dryas-Preboreal abrupt climatic transition (similar to 11,600 years ago) has been the subject of much debate. The carbon-14 (C-14) content of methane ((CH4)-C-14) should distinguish between wetland and clathrate...... contributions to this increase. We present measurements of (CH4)-C-14 in glacial ice, targeting this transition, performed by using ice samples obtained from an ablation site in west Greenland. Measured (CH4)-C-14 values were higher than predicted under any scenario. Sample (CH4)-C-14 appears to be elevated...

  2. Translocation of 14C in adventitiously rooting Calluna vulgaris on peat

    International Nuclear Information System (INIS)

    Wallen, B.

    1983-01-01

    Seasonal variation in translocation of 14 C-labelled assimilates showed that 14 C-translocation within woody tissue was mainly limited to the phytomass produced during the last eight years. Independent of overgrowth of basal stem segments or decumbent sections by Sphagnum, or of subsequent adventitious rooting, the allocation followed a negative exponential from the assimilating units down the plant, and reached negligible values in 8-yr-old wood. Translocation to fine roots was however, mainly restricted to the shallow roots. Already at ca. 10 cm depth, the fine roots contained only about 5% of the concentration in the fine roots in the surface. During spring and autumn translocation to below ground parts dominated. During summer the main translocation was within the above ground green shoots and flowers. Here most of the allocated 14 C was irreversibly bound. There were only weak indications of accumulation of moblie 14 C-compounds in the woody parts near the soil surface. (author)

  3. Study on "1"4C content in post-irradiation graphite spheres of HTR-10

    International Nuclear Information System (INIS)

    Wang Shouang; Pi Yue; Xie Feng; Li Hong; Cao Jianzhu

    2014-01-01

    Since the production mechanism of the "1"4C in spherical fuel elements was similar to that of fuel-free graphite spheres, in order to obtain the amount of "1"4C in fuel elements and graphite spheres of HTR-10, the production mechanism of the "1"4C in graphite spheres was studied. The production sources of the "1"4C in graphite spheres and fuel elements were summarized, the amount of "1"4C in the post-irradiation graphite spheres was calculated, the decomposition techniques of graphite spheres were compared, and experimental methods for decomposing the graphite spheres and preparing the "1"4C sample were proposed. The results can lay the foundation for further experimental research and provide theoretical calculations for comparison. (authors)

  4. Dissolved Organic Carbon 14C in Southern Nevada Groundwater and Implications for Groundwater Travel Times

    Energy Technology Data Exchange (ETDEWEB)

    Hershey, Ronald L. [Nevada University, Reno, NV (United States). Desert Research Institute; Fereday, Wyall [Nevada University, Reno, NV (United States). Desert Research Institute; Thomas, James M [Nevada University, Reno, NV (United States). Desert Research Institute

    2016-08-01

    Dissolved inorganic carbon (DIC) carbon-14 (14C) ages must be corrected for complex chemical and physical reactions and processes that change the amount of 14C in groundwater as it flows from recharge to downgradient areas. Because of these reactions, DIC 14C can produce unrealistically old ages and long groundwater travel times that may, or may not, agree with travel times estimated by other methods. Dissolved organic carbon (DOC) 14C ages are often younger than DIC 14C ages because there are few chemical reactions or physical processes that change the amount of DOC 14C in groundwater. However, there are several issues that create uncertainty in DOC 14C groundwater ages including limited knowledge of the initial (A0) DOC 14C in groundwater recharge and potential changes in DOC composition as water moves through an aquifer. This study examines these issues by quantifying A0 DOC 14C in recharge areas of southern Nevada groundwater flow systems and by evaluating changes in DOC composition as water flows from recharge areas to downgradient areas. The effect of these processes on DOC 14C groundwater ages is evaluated and DOC and DIC 14C ages are then compared along several southern Nevada groundwater flow paths. Twenty-seven groundwater samples were collected from springs and wells in southern Nevada in upgradient, midgradient, and downgradient locations. DOC 14C for upgradient samples ranged from 96 to 120 percent modern carbon (pmc) with an average of 106 pmc, verifying modern DOC 14C ages in recharge areas, which decreases uncertainty in DOC 14C A0 values, groundwater ages, and travel times. The HPLC spectra of groundwater along a flow path in the Spring Mountains show the same general pattern indicating that the DOC compound composition does not change along this flow path

  5. Mineralization of 14C-Pirimiphos-Methyl in Soil Under Aerobic and Anaerobic Conditions

    International Nuclear Information System (INIS)

    Zayed, S.M.A.D.; Farghly, M.; El-Maghrby, S.

    2006-01-01

    The mineralization of 14 C-ring labelled pirimiphos-methyl in clay loam soil was determined in a three months laboratory incubation period under anaerobic and aerobic conditions. Evolution of 14 CO2 increased with time and reached 9.2% and 12 %, of the initial 14 C-concentration , within 90 days in case of anaerobic and aerobic conditions, respectively, at that time, soil contained about 61.5% of the applied dose as extractable residues under anaerobic conditions and 59% under aerobic conditions. the unextractable pesticide residues gradually increased with time and the highest binding capacity of about 11%-13% was observed after 90 days of incubation. the total 14 C-activity recovered from soil was generally between 82% and 92% of the applied radiocarbon. the nature of methanolic 14 C-residues was determined by chromatographic analysis and the results revealed the presence of pirimiphos- methyl as a main product together with its phenol. the principle of radio-respirometry has been used for evaluating the effect of different application rates of pirimiphos-methyl on soil microbial activity using U- 14 C-glucose as a substrate. At two concentrations used, pirimiphos-methyl showed an inhibition in the rate of 14 Co2 evolution over 14 days of incubation as a result of oxidation of 14 C-glucose by microorganisms especially in case of high concentration

  6. Cristalización de vidrios ricos en sílice preparados mediante sol-gel en el sistema alúmina-circona-sílice

    Directory of Open Access Journals (Sweden)

    Popa, M.

    2004-02-01

    Full Text Available The crystallization of ZrSiO4 and its evolution with temperature from chemically homogeneous alumina-silica-zirconia powders prepared by sol-gel method from alcoxide mixtures was studied in the silica-rich region. A glass with the same composition was obtained by quenching in water from the melt. The gel-glasses evolution and microstructure were studied by means of XRD, IR and SEM/EDX, in the range of temperatures up to 1650oC. The materials consisted mainly of amorphous phase up to 1200oC, at which partial crystallization of cristobalite was observed. IR spectroscopy analysis showed zircon bands after thermal treatment at 1200oC. The crystallization of zircon and zirconia particles at 1550oC was confirmed by SEM/EDX analysis. At 1650oC the only stable crystalline phase observed after 40 h of thermal treatment was zircon.

    La cristalización de ZrSiO4 y su evolución con la temperatura se ha estudiado en la región rica en sílice, a partir de polvos amorfos y químicamente homogéneos de alumina-sílice-circona, preparados mediante método sol-gel usando mezclas de alcóxidos. Se obtuvo un vidrio con idéntica composición mediante enfriamiento rápido por inmersión en agua del material fundido. La evolución y la microestructura de los vidrios obtenidos se estudió mediante difracción de rayos X, infrarrojos, microscopía electrónica de barrido y análisis químico, en el rango de temperaturas hasta 1650oC. Los materiales están formados principalmente por fase amorfa hasta 1200oC, temperatura a la cual se observa la cristalización parcial de cristobalita. El análisis por espectroscopía de infrarrojos muestra bandas de circón en muestras tratadas térmicamente por encima de 1200oC. Las observaciones mediante microscopía electrónica confirman la cristalización de partículas de circón y circona a 1550oC. A 1650oC la cristobalita ha fundido y la única fase cristalina estable detectada mediante XRD tras 40 h a esta temperatura

  7. Measurement of {sup 14}C/{sup 12}C ratios in plant samples that were affected by the Fukushima nuclear accident

    Energy Technology Data Exchange (ETDEWEB)

    Hashimoto, Risa; Inoue, Aki; Muramatsu, Yasuyuki [Gakushuin University, 1-5-1 Mejiro, Toshima-ku, Tokyo, 171-8588 (Japan); Matsuzaki, Hiroyuki [The University of Tokyo, Micro Analysis Laboratory, Tandem Accelerator, 2-11-16 Yayoi, Bunkyo-ku, Tokyo, 113-0032 (Japan)

    2014-07-01

    In nature, {sup 14}C is produced by cosmic ray reactions in the upper atmosphere, and its production is influenced by the flux of cosmic rays. This nuclide is also released into the atmosphere by anthropogenic sources such as nuclear weapons testing and a nuclear accident. The produced {sup 14}C immediately becomes {sup 14}CO{sub 2} and it is absorbed by plants through photosynthesis. Therefore, plants are reflected by atmospheric {sup 14}C levels at that time. Although there are many papers reporting the release of several nuclides by the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident occurred in March, 2011, it is not clear whether appreciable amounts of {sup 14}C were released into the environment due to the accident. In this study, we focus on {sup 14}C levels in plant samples collected from several locations in Fukushima Prefecture (Okuma, Namie, Iitate, and Fukushima-city) and examine the possible influence on the {sup 14}C revels in plants. Since cedars and pines are evergreen, the leaves should have been contaminated at the time of the accident. We analyzed old leaves, which were grown before the accident, and new leaves, which were grown after the accident. Both old and new leaves were collected in the same branch. In order to compare delta {sup 14}C values in leaves collected from Fukushima Prefecture with background values, we have used plant samples collected from remote areas such as Chiba and Niigata Prefectures. The samples were dried, pulverized in a blender and homogenized. Then samples were placed between copper oxide wires in a quarts tube, burned and oxidized. The produced CO{sub 2} mixed gases were purified in a vacuum line. To prepare a graphite target for AMS, the purified CO{sub 2} was reduced. {sup 14}C/{sup 12}C ratio in the graphite was measured by AMS at the University of Tokyo or Japan Atomic Energy Agency. Analytical results showed that delta {sup 14}C values in plant samples collected from the highly contaminated areas such as

  8. Production and release of {sup 14}C from a swimming pool reactor

    Energy Technology Data Exchange (ETDEWEB)

    Krishnamoorthy, T M [Bhabha Atomic Research Centre, Mumbai (India). Environmental Assessment Div.; Sadarangani, S H [Bhabha Atomic Research Centre, Mumbai (India). Radiation Safety Systems Div.; Doshi, G R [Bhabha Atomic Research Centre, Bombay (India). Health Physics Div.

    1994-04-01

    The annual production rate of {sup 14}C in the Apsara swimming pool reactor works out to be about 2.94 mCi. The concentration distribution of {sup 14}C in different compartments viz. pool water, reactor hall air and ion-exchange resin ranged from 200 to 440 pCi/l, 0.09 to 0.38 pCi/l, an average concentration of 8.16 pCi/g respectively. The mean residence time of {sup 14}C in pool water is evaluated to be about 7 days taking into account various sinks. The study revealed atmospheric exchange at the air-water interface as the dominant process responsible for the loss of {sup 14}C from the pool water. (author). 7 refs., 2 figs., 4 tabs.

  9. Synthesis of dimethyl-1,1 guanylguanidine-{sup 14}C-2,4 (dimethyl-1-1 biguanide) hydrochloride; Synthese du chlorhydrate de dimethyl-1,1 guanylguanidine {sup 14}C-2,4 (dimethyl-1-1 biguanide)

    Energy Technology Data Exchange (ETDEWEB)

    Herbert, M; Pichat, L [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1961-07-01

    A description of the synthesis of dimethyl-1,1 guanylguanidine-{sup 14}C-2,4 hydrochloride passing through the {sup 14}C{sub 2} dicyandiamide. The overall yield with respect to Ba{sup 14}CO{sub 3} is 38 per cent. (author) [French] Description de la synthese du chlorhydrate de dimethyl-1,1 guanylguanidine {sup 14}C-2,4 par l'intermediaire de la dicyandiamide {sup 14}C{sub 2}. Le rendement global par rapport a {sup 14}CO{sub 3}Ba est de 38 pour cent. (auteur)

  10. Simple measurement of 14C in the environment using gel suspension method

    International Nuclear Information System (INIS)

    Wakabayashi, Genichiro; Oura, Hirotaka; Nagao, Kenjiro; Okai, Tomio; Matoba, Masaru; Kakiuchi, Hideki; Momoshima, Noriyuki; Kawamura, Hidehisa

    1999-01-01

    A gel suspension method using N-lauroyl-L-glutamic-α, γ-dibutylamide as gelling agent and calcium carbonate as sample was studied and it was proved a more simple measurement method of 14 C in environment than the ordinary method. 100, 20 and 7 ml of sample could introduce 3.6, 0.72 and 0.252 g of carbon, respectively. When 100 ml and 20 ml of vial introduced the maximum carbon, the lower limit of detection was about 0.3 dpm/g-C and 0.5 dpm/g-C, respectively. These values showed that this method was able to determine 14 C in the environment. The value of sample has been constant for two years or more. This fact indicated the sample prepared by this method was good for repeat measurement and long-term storage. Many samples prepared by the same calcium carbonate showed almost same values. The concentrations of 14 C in the growth rings of a tree and in rice in the environment were determined and the results agreed with the values in the references. From these above results, this method is more simple measurement method of 14 C in the environment than the ordinary method and can apply to determine 14 C in and around the nuclear installation. (S.Y.)

  11. Intracavity optogalvanic spectroscopy. An analytical technique for 14C analysis with subattomole sensitivity.

    Science.gov (United States)

    Murnick, Daniel E; Dogru, Ozgur; Ilkmen, Erhan

    2008-07-01

    We show a new ultrasensitive laser-based analytical technique, intracavity optogalvanic spectroscopy, allowing extremely high sensitivity for detection of (14)C-labeled carbon dioxide. Capable of replacing large accelerator mass spectrometers, the technique quantifies attomoles of (14)C in submicrogram samples. Based on the specificity of narrow laser resonances coupled with the sensitivity provided by standing waves in an optical cavity and detection via impedance variations, limits of detection near 10(-15) (14)C/(12)C ratios are obtained. Using a 15-W (14)CO2 laser, a linear calibration with samples from 10(-15) to >1.5 x 10(-12) in (14)C/(12)C ratios, as determined by accelerator mass spectrometry, is demonstrated. Possible applications include microdosing studies in drug development, individualized subtherapeutic tests of drug metabolism, carbon dating and real time monitoring of atmospheric radiocarbon. The method can also be applied to detection of other trace entities.

  12. {sup 14}C content in aerosols in Mexico City

    Energy Technology Data Exchange (ETDEWEB)

    Gómez, V.; Solís, C.; Chávez, E.; Andrade, E.; Ortiz, M.E.; Huerta, A.; Aragón, J.; Rodríguez-Ceja, M. [Instituto de Física, Universidad Nacional Autónoma de México, Apartado Postal 20-364, México, D.F. 01000 (Mexico); Martínez, M.A. [Facultad de Ciencias, Universidad Nacional Autónoma de México (Mexico); Ortiz, E. [Universidad Autónoma Metropolitana-Azcapotzalco, Av. San Pablo 180, C. P. 02200 México, D.F. (Mexico)

    2016-03-15

    {sup 14}C-AMS of total carbon was determined in aerosols (PM{sub 10} fraction), collected in Mexico City during two weeks from 21 November to 3 December 2012. Other tracers such as total carbon (TC), organic carbon (OC), elemental carbon (EC) and trace element contents were also determined. F{sup 14}C values varied from 0.39 to 0.48 with an average of 0.43. These values are slightly lower than those previously obtained for PM{sub 2.5} in 2003 and 2006 and reflect a high contribution of fossil CO{sub 2} to the carbonaceous matter in aerosols from Mexico City. In contrast, from 2006 to 2012 PM{sub 10} increased; EC, Ca, Ti and Fe concentrations remained constant, while OC, TC and K concentrations decreased. The use of potassium as an indicator of biomass burning showed that this source was negligible during this campaign. Combined analytical approaches allowed us to distinguish temporal variations of anthropogenic and natural inputs to the F{sup 14}C.

  13. Behaviour of 14C-DDT in Sudan Gezira soil

    International Nuclear Information System (INIS)

    Abdalla, A.M.; El-Zorgani, G.A.

    1988-01-01

    Field cylinders as described in the model experiment for determination of 14 C-DDT in Sudan Gezira soil were prepared and samples were collected for determination of 14 C-activity at various intervals. About 83-87% of the applied radioactivity was recovered in the extracts from the top 10 cm layer of soil. The loss rate of the chemical from soil increased with time apparently by volatilization and thermal degradation due to high soil temperature, intensive solar radiation and low soil organic matter. This resulted in a half-life of approx. 5 weeks. The major part of the chemical and possible metabolites were detected in the top 10 cm layer. Approximately 8-10% of the applied 14 C was detected in samples collected after 16-20 weeks. TLC and autoradiography indicated the presence of p,p'-DDT and p,p'-DDE as the major metabolite. Also traces of TDE were detected in some samples. These results showed that under Sudanese tropical conditions, DDT dissipates very rapidly in soils compared to dissipation in temperate regions. (author). 6 refs, 2 tabs

  14. Distribution of Δ14C in western North Pacific and tracing carbons of human origin

    International Nuclear Information System (INIS)

    Aramaki, Takafumi; Mizushima, Toshihiko; Togawa, Orihiko; Kuji, Tomoyuki

    2001-01-01

    Seawater were collected at six points, 0deg to 48degN around 165degE. Dissolved inorganic carbonates was reduced into graphite. The ratio C-11/C-12 was measured by the accelerator mass analyzer. 14 C concentration was calculated from δ 13 C value calculated from the 13 C/ 12 C ratio. 14 C resulting from the nuclear weapon test was calculated by comparing estimated 14 C and real 14 C concentration. It was compared with that in 1970s. 14 Cbomb has dissolved into North Pacific Intermediate Water in Arctic latitude, which has moved to Mid-latitude. (A. Yamamoto)

  15. Special Analysis: Revised 14C Disposal Limits for the Saltstone Disposal Facility

    International Nuclear Information System (INIS)

    Kaplan, D.I.

    2004-01-01

    The Saltstone Special Analysis calculated a limit for 14C based on the atmospheric pathway of 52 pCi/mL using some very conservative assumptions. This was compared to the estimated Low Curie Salt concentration of 0.45 pCi/mL and since the limit was two orders of magnitude greater than the estimated concentration, the decision was made that no further analysis was needed. The 14C concentration in Tank 41 has been found to be much greater than the estimated concentration and to exceed the limit derived in the Special Analysis. A rigorous analysis of the release of 14C via the air pathway that considers the chemical effects of the Saltstone system has shown that the flux of 14C is significantly less than that assumed in the Special Analysis. The net result is an inventory limit for 14C that is significantly higher than that derived in the Special Analysis that will also meet the performance objectives of DOE Order 435.1

  16. [1-14C]Glycolate metabolism and serine biosynthesis in soybean plants

    International Nuclear Information System (INIS)

    Calmes, J.; Viala, G.; Latche, J.C.; Cavalie, G.

    1977-01-01

    [1- 14 C]Glycolate metabolism was examined in leafy shoots of soybean plants (Glycine max (L.) Merr., var. Adepta). Only small amounts of 14 C were incorporated into evolved carbon dioxide and glucidic compounds. Free and protein glycine was labelled but higher levels of radioactivity were found in free serine. Changes in the distribution of 14 C with time showed that metabolic conversion glycollate → glycine → serine occurred very early and serine biosynthesis was more important in the shoot than in the leaves. Carbon dioxide labelling was always slight compared to serine labelling. These data suggest strong relations between glycollate and nitrogen metabolism

  17. 14CO2 fixation and allocation of 14C into major biochemical fractions in different parts of Indian mustard (Brassica juncea)

    International Nuclear Information System (INIS)

    Subrahmanyam, D.; Rathore, V.S.

    1993-01-01

    14CO2 fixation and transport of 14C-photosynthates amongst different parts of Indian mustard (Brassica juncea) and the incorporation of 14C into major chemical fractions in different plant parts was studied at ripening stage. Stem and pod together contributed 70 % of the total 14C fixed by the plant. In all plant parts neutral saccharide fraction contained maximum radioactivity immediately after exposing plants to 14CO2. After 24 h, the radioactivity in this fraction declined considerably due to translocation or conversion into other fractions. Concomitantly radioactivity in lipids and pigments, residue and starch fractions increased after 24 h. The 14C allocation patterns in stem and leaves were similar. However, in pods very high radioactivity was recovered from amino and organic acid fractions indicating the presence of active phosphoenolpyruvate carboxylase in pod walls

  18. 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.).

  19. Translocation of 14-C in ponderosa pine seedlings

    Science.gov (United States)

    Robert R. Ziemer

    1971-01-01

    The movement of 14-C from the old needles to the roots, and later to the new needles, was measured in 2-year-old ponderosa pine seedlings. The seedlings were in one of three growth stages at the time of the feeding of 14-CO-2: 9 days before spring bud break with no root activity; 7 days before spring bud break with high root activity; and 7 days after spring bud break...

  20. Seasonal variations of {sup 14}C and δ{sup 13}C for cave drip waters in Ryugashi Cave, Shizuoka Prefecture, central Japan

    Energy Technology Data Exchange (ETDEWEB)

    Minami, Masayo, E-mail: minami@nendai.nagoya-u.ac.jp [Center for Chronological Research, Nagoya University, Nagoya 464-8602 (Japan); Kato, Tomomi [Graduate School of Environmental Studies, Nagoya University, Nagoya 464-8601 (Japan); Horikawa, Keiji [Department of Environmental Biology and Chemistry, Toyama University, Toyama 930-8555 (Japan); Nakamura, Toshio [Center for Chronological Research, Nagoya University, Nagoya 464-8602 (Japan)

    2015-11-01

    Speleothem {sup 14}C has recently emerged as a potentially powerful proxy for hydrology changes in comparison with atmospheric {sup 14}C calibration curve, rather than as a direct dating tool, apart from a time marker using bomb peak of {sup 14}C. Some possible causes for the relationship between speleothem {sup 14}C content (or dead carbon fraction: DCF) and karst hydrology have been proposed, such as changes in temperature, precipitation, drip water flow dynamics, cave air ventilation, soil air pCO{sub 2}. In this study, we investigated seasonal variation in {sup 14}C and δ{sup 13}C of drip water in Ryugashi Cave, Shizuoka Prefecture, central Japan, to examine the causes of the {sup 14}C and δ{sup 13}C variations in a speleothem. The results show that different {sup 14}C concentrations and δ{sup 13}C values of drip water from the Ryugashi Cave, were exhibited at different sites of the Caves No. 1, No. 3, and No. 4, which have different temperature, air pCO{sub 2}, and flow paths. Further, the {sup 14}C and δ{sup 13}C of drip waters showed seasonal variations at all sites, which were lower in fall and winter, and higher in spring and summer, though the extent of the variations was different among the sites. The {sup 14}C in drip waters tended to be correlated with the drip rates: {sup 14}C tended to be higher in drip waters with higher drip rates, and also correlated with rainfall amount around the Ryugashi Cave, especially for the drip waters in Cave No. 3, which are considered to have simpler flow paths. The increase in rainfall amount could bring the increase in drip rate of drip water, and then the decrease in interaction between solution and karst, resulting in {sup 14}C increase (DCF decrease) in drip water. Accordingly, the reconstruction of precipitation could be performed using {sup 14}C variation in a speleothem formed by drip water with simple flow dynamics.

  1. Radioactivity measurement of barium carbonate [14C] by liquid scintillation counting

    International Nuclear Information System (INIS)

    Kobayashi, Katsutoshi; Hoizumi, Kiyoshi

    1985-03-01

    Two methods of sample preparation for the measurement of specific activity of BaCO 3 [ 14 C] by external standard method in liquid scintillation counting were studied. BaCO 3 [ 14 C] was decomposed by perchloric acid solution and generated CO 2 [ 14 C] was absorbed by ethylene glycol monomethyl ether solution of monoethanolamine as the method 1 or aqueous sodium hydroxide as the method 2. In order to prepare the sample solution of adequate radioactivity concentration, these carbonate solutions by the methods 1 and 2 were diluted with the suitable organic solvent and distilled water respectively. One tenth millilitre of these sample solutions was added into 10 ml of PPO-toluene scintillator containing 0.1 ml of monoethanolamine in a counting vial and homogeneously dissolved with ethyl alcohol. The results of the radioactivity measurement of BaCO 3 [ 14 C] based on the different method agreed within 5 % and the counting rate was found to be stable for as long as 7 deays or more. Both methods of preparation are suitable for the routine measurement because of their simplicity and feasibility. In the case of method 2, the liquid radioactive waste is almost inorganic solution and recovery in the form of BaCO 3 [ 14 C] is easily performed, so that this method is very advantageous from the view point of the radioactive waste treatement. (author)

  2. Incineration of radioactive wastes containing only C-14 and H-3

    International Nuclear Information System (INIS)

    Garcia, Corazon M.

    1992-01-01

    C-14 and H-3 arc popularly used in chemical and biological research institutions in the Philippines. Most of the solid radioactive wastes generated by these institutions consist of combustible materials such as paper and accumulated environmental samples. Liquid wastes usually contain organic substances. The method proposed for managing C-14 and H-3 wastes is incineration which is expected to provide an acceptable means of disposal for C-14 and H-3 and their hazardous organic constituent. In the incineration process) the radioactively contaminated waste will be mixed with non-radioactive combustible wastes to lower the activity concentration and to improve the efficiency of combustion which will be carried out in a locally fabricated drum incinerator. The calculations presented determines the concentration limit for the incinerable wastes and the restriction on specific activity of the particles of the incinerable wastes containing C-14 or H-3 on the basis of the accepted air concentration and on the annual dose limit for an average radiation worker in the country. In the calculations for C-14, considerations were taken on the exposure received from the deposition of radioactive particles in the lungs containing unoxidized carbon. Calculations for H-3, however, is based on the assumption that the concentration of the radionuclide in the body water is the same as that in the environment. (author)

  3. Dermal absorption and distribution of 14 C carbaryl in wistar rats

    International Nuclear Information System (INIS)

    Tos-Luty, S.; Tokarska-Rodak, M.; Latuszynska, J.; Przebirowska, D.

    2001-01-01

    The level of 14 C carbaryl was determined in blood (leukocytes, erythrocytes, all blood cells, plasma) and organs (brain, heart, lungs, liver, spleen, skin at the site of exposure) of male Wistar rats after dermal administration. The application liquid was 14 C carbaryl solution in 96% ethyl alcohol. This preparation, possessing an activity of 670 kBq/ml, containing 1.67 mg of carbaryl, was applied to the skin of the tail according to Massmann's method in own modification. The amount of the preparation per 1 cm 2 of the tail skin was 0.19 mg of carbaryl (74.4 kBq). The tails of experimental rats were exposed to 14 C carbaryl by soaking for 4 h daily: once, twice or three times. Beta radiation from 14 C was measured in homogenized organs (brain, heart, lungs, liver, skin) and in blood by computer controlled Wallac scintillation counter Model 1409, using Multi Calc software. The dermal absorption of carbaryl at the site of exposure and in the surrounding area of about 2 cm was observed already during 4 hour exposure. Carbaryl reached plasma within 4 h of a single dermal exposure and penetrated into leukocytes, erythrocytes, heart, liver, lung, kidney and brain. The largest amount of 14 C carbaryl, about 2% of absorbed dose, was detected in liver. (author)

  4. Synthesis of /sup 14/C- and /sup 35/S-labelled 2-mercaptobenzimidazoles

    Energy Technology Data Exchange (ETDEWEB)

    Doerge, D R

    1988-09-01

    /sup 14/C- and /sup 35/S-labelled 2-mercaptobenzimidazole and 1-methyl-2-mercaptobenzimidazole were synthesized from /sup 14/C-carbon disulfide, /sup 35/S-thiourea, /sup 14/C-methyl iodide and /sup 35/S-thiourea, respectively, for use in studies on the mechanism of action of antithyroid drugs. The products were purified by chromatography on silica and isolated with radiochemical purities of greater than 98%, yields of 45-77% and specific activities of 2.1-5.3 mCi/mmole.

  5. The Moessbauer effect in Fe(III) HEDTA, Fe(III) EDTA, and Fe(III) CDTA compounds

    International Nuclear Information System (INIS)

    Prado, F.R.

    1989-01-01

    The dependence of Moessbauer spectra with pH value of Fe(III)HEDTA and Fe(III)CDTA compounds is studied. Informations on formation processes of LFe-O-FeL (L=ligand) type dimers by the relation of titration curves of Fe(III)EDTA, Fe(III)HEDTA and Fe(III)CDTA compounds with the series of Moessbauer spectra, are obtained. Some informations on Fe-O-Fe bond structure are also obtained. Comparing the titration curves with the series of Moessbauer spectra, it is concluded that the dimerization process begins when a specie of the form FeXOH α (X = EDTA, HEDTA, CDTA; α = -1, -2) arises. (M.C.K.) [pt

  6. 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

  7. Intra cellular distribution of 8-14C-puromycin aminonucleoside in ultraviolet irradiated Escherichia coli

    International Nuclear Information System (INIS)

    Sideropoulos, A.S.

    1976-01-01

    The uptake of 8- 14 C-puromycin aminonucleoside (8- 14 C-PAN) was studied in ultraviolet (UV) irradiated strains of E. coli B/r hcr + and hcr - . The cells took up only 0.1-0.3% of the 8- 14 C-PAN present in the medium when grown in minimal (M9) containing 8- 14 C-PAN. When ethylenedinitrilotetra-acetic acid (EDTA) treated E. coli cells are placed in a medium containing 8- 14 C-PAN, the total concentration of 8- 14 C-PAN in the cell reaches 43-54% of the medium within 30 min of incubation. Almost all 8- 14 C-PAN can be dialyzed from cells exposed in the absence of an energy source, but cells metabolizing in M9 medium during exposure can retain up to 30% of their internal concentration. Bacteria grown in the presence of 8- 14 C-PAN, accumulated the radioactive material intracellulary in three forms, namely, unbound, reversibly bound (dialyzable) and irreversibly bound to the protein (nondialyzable). Approx. 70-77% of the irreversibly bound radioactive material linked with the protein fraction was released by treatment with a protease. Addition of PAN into the post-irradiation medium of EDTA-treated hcr + cells, increased UC induced mutation rates. Antimutagenic purine ribosides decreased the final level of 8- 14 C-PAN accumulated by the cells. Decreases in 8- 14 C-PAN uptake in the presence of antimutagens correspond to reductions in the rate of mutation to streptomycin resistance induced by UV light. Therefore, protein bound PAN appears to be the relevant component in the enhancement of UV induced mutation by this drug

  8. Influence of V/III growth flux ratio on trap states in m-plane GaN grown by ammonia-based molecular beam epitaxy

    International Nuclear Information System (INIS)

    Zhang, Z.; Arehart, A. R.; Hurni, C. A.; Speck, J. S.; Ringel, S. A.

    2012-01-01

    Deep level transient spectroscopy (DLTS) and deep level optical spectroscopy (DLOS) were utilized to investigate the behavior of deep states in m-plane, n-type GaN grown by ammonia-based molecular beam epitaxy (NH 3 -MBE) as a function of systematically varied V/III growth flux ratios. Levels were detected at E C - 0.14 eV, E C - 0.21 eV, E C - 0.26 eV, E C - 0.62 eV, E C - 0.67 eV, E C - 2.65 eV, and E C - 3.31 eV, with the concentrations of several traps exhibiting systematic dependencies on V/III ratio. The DLTS spectra are dominated by traps at E C - 0.14 eV and E C - 0.67 eV, whose concentrations decreased monotonically with increasing V/III ratio and decreasing oxygen impurity concentration, and by a trap at E C - 0.21 eV that revealed no dependence of its concentration on growth conditions, suggestive of different physical origins. Higher concentrations of deeper trap states detected by DLOS with activation energies of E C - 2.65 eV and E C - 3.31 eV in each sample did not display measureable sensitivity to the intentionally varied V/III ratio, necessitating further study on reducing these deep traps through growth optimization for maximizing material quality of NH 3 -MBE grown m-plane GaN.

  9. Effect of gamma radiation on photosynthetic metabolism of Chlorella pyrenoidosa studied by 14{sup C}O{sub 2} assimilation; Estudio del efecto de la radiacion gamma sobre el metabolismo fotosintetico de Chlorella pyrenoidosa mediante asimilacion de 14{sup C}O{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Martin, C; Fernandez, J

    1983-07-01

    The effect of five dose of gamma radiation (10, 100, 500, 1000 and 5000 Gy) on photosynthetic activity and metabolism of the primary products of photosynthesis has been studied, on Chlorella pyrenoidoBa cultures, by 14{sup C}O{sub 2} assimilation. The photosynthetic assimilation rate is remarkably depressed after irradiation at 500, 1000 and 5000 Gy dose, which also produce a significant change in radioactivity distribution pattern of primary compounds from photosynthesis. No significant effects have been observed on photosynthetic metabolism after irradiation at 10 and 100 Gy. (Author) 19 refs.

  10. Synthesis of organic substances labelled with {sup 14}C and {sup 35}S; Syntheses de molecules organiques marquees par le carbone-14 et le soufre-35

    Energy Technology Data Exchange (ETDEWEB)

    Pichat, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    After a brief history of the development of the Section des Molecules marquees of the Frenchmic Energy Commission, the author gives an outline of the synthesis of the following labelled compounds: benzene {sup 14}C-6; phenyl-p-fluorophenyl, thienyl-2 {beta} alanines {beta} {sup 14}C; noradrenaline {beta} {sup 14}C (arterenol {beta} {sup 14}C), dotriacontane {sup 14}C-16-17, aminoethane sulfinic acid (hypotaurine {sup 35}S). (author)Fren. [French] Apres un bref historique du developpement de la Section des Molecules marquees du Commissariat a l'Energie Atomique fran is, l'auteur donne un resume des syntheses des composes marques suivants: benzene {sup 14}C-6; phenyl-p-fluorophenyl, thienyl-2 {beta} alamines {beta} {sup 14}C; noradrenaline {beta} {sup 14}C (arterenol {beta} {sup 14}C), dotriacontane {sup 14}C-16-17, acide aminoethane sulfinique (hypotaurine {sup 35}S). (auteur)

  11. Tracer experiment administering L-phenylalanine-U-{sup 14}C and L-tyrosine-U-{sup 14}C to the tissue slices of bamboo shoots

    Energy Technology Data Exchange (ETDEWEB)

    Kozukue, E. [Kenmei Women' s Junior Coll., Himeji, Hyogo (Japan); Mizuno, S.

    1987-09-15

    Uniformly {sup 14}C-labeled L-phenylalanine and L-tyrosine were administered to tissue slices of both top and base sections of bamboo shoots. Alcohol soluble substances were extracted and then separated into organic acid, sugar and amino acid fractions by ion exchange chromatography. The homogentisic acid fraction among the organic acids was collected by high-performance liquid chromatography (HPLC) and its radioactivity was measured, while the alcohol insoluble residue was used for the analysis of lignin aldehyde by the method of alkaline nitrobenzene oxidation. 1. The two labeled amino acids were steadily incorporated into the tissues during incubation and rapidly converted to organic acid, sugar and alcohol insoluble residue, especially the latter. 2. On determining the amount of phenylalanine converted to tyrosine, it was found that this was extremely small. 3. The incorporation of phenylalanine-U-{sup 14}C into alcohol insoluble residue was higher than that of tyrosine in both sections. 4. Although the conversion into lignin aldehyde from phenylalanine-U-{sup 14}C was higher than that from tyrosine-U-{sup 14}C, it was found that tyrosine incorporated into the shoots was converted to a remarkable extent for formation of lignin aldehyde. 5. The incorporation of phenylalanine and tyrosine into homogentisic acid was very low. From these results, we assume that the conversion of phenylalanine to tyrosine or of tyrosine to homogentisic acid is very small, and that a part of the high amount of tyrosine in the shoots may be used for formation of lignin.

  12. Synthesis of 20-14C 3β-hydroxy-5β-pregnan-20-one

    International Nuclear Information System (INIS)

    Garraffo, H.M.; Gros, E.G.

    1982-01-01

    20 - 14 C 3β-hydroxy-5β-pregnan-20-one was synthesised by condensing 3β-acetoxy-5β-androstan-17-one with potassium 14 C cyanide to produce cyanohydrin. This was dehydrated and the resulting unsaturated nitrile treated with methylmagnesiumiodide to produce hydroxypregnenone. Hydrogenation of this gave 14 C 3β-hydroxy-5β-pregnan-20-one. (U.K.)

  13. 14C-urea breath test for the detection of Helicobacter pylori

    NARCIS (Netherlands)

    Veldhuyzen van Zanten, S. J.; Tytgat, K. M.; Hollingsworth, J.; Jalali, S.; Rshid, F. A.; Bowen, B. M.; Goldie, J.; Goodacre, R. L.; Riddell, R. H.; Hunt, R. H.

    1990-01-01

    The high urease activity of Helicobacter pylori can be used to detect this bacterium by noninvasive breath tests. We have developed a 14C-urea breath test which uses 5 microCi 14C with 50 mg nonradioactive urea. Breath samples are collected at baseline and every 30 min for 2 h. Our study compared

  14. Radiocarbon C-14 dating - MINT experience

    International Nuclear Information System (INIS)

    Kamisah Alias

    2002-01-01

    The measurement of a radiocarbon date is a complex process which involved all the stages from advice given prior to submission of samples right through to reporting of results. The aim of our radiocarbon dating is to determine the residual 14 C content of a sample, the value of which is translated into an age that is an estimate of the time elapsed since the given sample was removed from the environment in which it had formed in equilibrium with respect to 14-C radioactive decay and metabolic assimilation. Carbon is obtained from carbon containing samples in the form of carbon dioxide, which is then reacted with lithium forming lithium carbide. The carbide is then hydrolysed to acetylene before it was polymerised to benzene using a high-efficiency vanadium-alumina-silica catalyst to produce benzene with up to 96% yield. Sample, background and modem standard activities are measured with a coincidence scintillation counter using in glass vials of 21 ml capacity. An improved chemical procedure was used to obtain and purify the benzene from the samples for measurement using a liquid scintillation counter. Radiocarbon dating measurements of samples collected reveal some results. The validity of the data have yet to be confirmed by the results of the measurements on two international control samples. (Author)

  15. Synthesis of 14C-labeled and stable isotope-labeled CGS 16617

    International Nuclear Information System (INIS)

    Chaudhuri, N.K.; Markus, B.; Sung Mingsang

    1988-01-01

    The synthesis of a 14 C-labeled and two stable isotope-labeled analogs of CGS 16617 is described. The synthetic method involved the preparation of tetrahydro-3-bromo-1-benzazepin-2-one, labeled with a 14 C or four deuterium atoms, followed by introduction of two side chains at 1- and 3-positions. The labeled bromobenzazepinones were prepared by Beckmann rearrangement of bromo-oximes of α-tetralones, obtained by cyclization of labeled benzenebutanoic acids. The 14 C-labeled acid was prepared by hydrolysis of the nitrile, prepared by reaction of 3-bromopropylbenzene and K 14 CN. The tetradeutero acid was prepared from ethyl phenylpropynoate by catalytic reduction of the triple bond with deuterium gas, followed by reduction of the deuterated ester with lithium aluminium hydride and conversion of the resulting alcohol into the carboxylic acid. The acetic acid side chain was introduced by N-alkylation with ethyl bromoacetate or ethyl bromoacetate-1, 2- 13 C 2 followed by hydrolysis, and the L-lysine side chain, by reaction with L-(-)-3-amino-ε-caprolactam followed by hydrolysis of the caprolactam ring. (author)

  16. Common fur and mystacial vibrissae parallel sensory pathways: 14C 2-deoxyglucose and WGA-HRP studies in the rat

    International Nuclear Information System (INIS)

    Sharp, F.R.; Gonzalez, M.F.; Morgan, C.W.; Morton, M.T.; Sharp, J.W.

    1988-01-01

    Stimulation of mystacial vibrissae in rows A,B, and C increased (14C) 2-deoxyglucose (2DG) uptake in spinal trigeminal nucleus pars caudalis (Sp5c) mostly in ventral portions of laminae III-IV with less activation of II and V. Stimulation of common fur above the whiskers mainly activated lamina II, with less activation in deeper layers. The patterns of activation were compatible with an inverted head, onion skin Sp5c somatotopy. Wheatgerm Agglutinin-Horseradish Peroxidase (WGA-HRP) injections into common fur between mystacial vibrissae rows A-B and B-C led to anterograde transganglionic labeling only of Sp5c, mainly of lamina II with less label in layer V, and very sparse label in III and IV. WGA-HRP skin injections appear to primarily label small fibers, which along with larger fibers, were metabolically activated during common fur stimulation. Mystacial vibrissae stimulation increased 2DG uptake in ventral ipsilateral spinal trigeminal nuclei pars interpolaris (Sp5i) and oralis (Sp5o) and principal trigeminal sensory nucleus (Pr5). Common fur stimulation above the whiskers slightly increased 2DG uptake in ventral Sp5i, Sp5o, and possibly Pr5. The most dorsal aspect of the ventroposteromedial (VPM) nucleus of thalamus was activated contralateral to whisker stimulation. Stimulation of the common fur dorsal to the whiskers activated a region of dorsal VPM caudal to the VPM region activated during whisker stimulation. This is consistent with previous data showing that ventral whiskers and portions of the face are represented rostrally in VPM, and more dorsal whiskers and dorsal portions of the face are represented progressively more caudally in VPM. Mystacial vibrissae stimulation activated the contralateral primary sensory SI barrelfield cortex and a separate region in the second somatosensory SII cortex

  17. Historical 14C measurements from the Atlantic, Pacific and Indian Oceans. Final report

    International Nuclear Information System (INIS)

    Fairhall, A.W.; Young, A.W.

    Atmospheric nuclear testing produced a dramatic increase in the level of 14 C in atmospheric CO 2 . Since the tropospheric residence time of 14 C is on the order of a few years before being transferred to the sea, it appeared that a study of the distribution of the excess 14 C in the sea and its change with time would give valuable insight into such problems as the rate of CO 2 exchange between the atmosphere and the sea and its dependence on wind speed over the sea surface; the rate of transfer by oceanic mixing processes of contaminants, including fallout radionuclides introduced initially into the mixed surface layer of the sea, into the deep sea; the rate of bottom water formation at high latitudes and subsequent advective transport from these source regions into the deep sea. Therefore a 14 C sampling program was initiated. A method was developed for stripping CO 2 from sea water on board ship. The assay for 14 C was performed by a radiocarbon gas proportional counter. Information on temperature and salinity at the various sampling depths as well as total CO 2 and absolute concentration of 14 C is tabulated

  18. Persistence and fate of soil applied 14C-lindane in a maize ecosystem

    International Nuclear Information System (INIS)

    Yeboah, P.O.; Montford, K.G.; Apoh, W.; Dodoo, S.

    1997-01-01

    14 C-lindane applied to soil surface in a maize ecosystem (one month after planting) was taken up by the plant. Within the first 25 days of treatment, 14 C-lindane or its metabolites were found within the entire plant with the greatest concentration in lower leaves (from the ground level); and a sharp build up of lindane concentration towards the tip of each leaf. Radioactivity and hence pesticide concentration was uniformly distributed in the plant with time; to the extent that measurable levels of 14 C-compounds were detected in the tussel cob and the grain. This indicated that soil applied lindane was available to the maize plant. The persistence of 14 C-lindane in soils of variable organic matter content was also studied. Evidence is presented to show that 14 C-lindane dissipated faster in soils of lower organic matter content. Levels of surface applied pesticides that became bound in the soil increased with time after application and also with increasing organic matter content. 14 C-activity was mainly associated with the top soil layer (0-30 mm). (author). 7 refs, 7 figs

  19. Diseño y prototipaje del álabe para un miniaerogenerador mediante impresión 3D

    OpenAIRE

    Roy Mota, Andrea

    2017-01-01

    El objetivo de este proyecto consiste en el diseño de una maqueta de álabe para un mini aerogenerador y su posterior fabricación con PLA mediante la tecnología de impresión 3D no industrial. Para conseguirlo se creó una hoja de cálculo que torna la superficie del ala; se analizó la impresora 3D y se diseñó la estructura interna del aspa para dotarlo de resistencia según sus límites de impresión de la impresora mediante el programa Siemens Unigraphics NX10; se simularon los esfuerzos y a parti...

  20. Desarrollo de un escáner 3D mediante cámaras estereoscópicas e iluminación láser

    OpenAIRE

    Cristina, Federico; Dapoto, Sebastián H.; Vegas, Javier; Artola, Verónica; Russo, Claudia Cecilia; Abásolo Guerrero, María José

    2007-01-01

    Los dispositivos de escaneo tridimensional permiten obtener modelos de objetos utilizando distintas técnicas de captura. Esta tarea puede ser llevada a cabo por ejemplo mediante estereovisión, el cual es un método de reconstrucción 3D a partir de fotografías. Las técnicas de reconstrucción 3D mediante luz se basan en la proyección de un patrón de luz conocido sobre una escena y a partir del análisis de la proyección puede deducirse la forma de los objetos. De esta manera, basándose en la info...

  1. Emission of {sup 14}C by the Almirante Alvaro Alberto Nuclear Power Plant 1 and 2 and their local effects on the environmental levels; Emissao de {sup 14}C pelas unidades 1 e 2 da Central Nuclear Almirante Alvaro Alberto (CNAAA) e seu efeito local nos niveis ambientais

    Energy Technology Data Exchange (ETDEWEB)

    Dias, Cintia Melazo

    2006-07-01

    {sup 14}C is a is a long-lived beta-emitting nuclide (T{sub 1/2} = 5730 years) produced naturally in the upper atmosphere as a result of reactions between neutrons and stable {sup 14}N({sup 14}N(n,p){sup 14}C). Although in a lesser extent, nuclear power plants produce {sup 14}C as well during their routine operation. Since it is converted in {sup 14}CO{sub 2} and mixed throughout the atmosphere, it is incorporated into plant tissues, via photosynthesis process, and hence in food chain. Because of the biological importance of {sup 14}C and long half-life, it is of interest to quantify the amounts released by nuclear industry. The Brazilian nuclear central named Nuclear Central Admiral Alvaro Alberto (CNAAA) has two nuclear reactors of PWR type in operation, Angra I (657 MWe) and Angra II (1350 MWe), and one under construction, Angra III (1309 MWe PWR). The aim of this study was to determine the strength of the sources and the {sup 14}C content in the environment through analyses of air, vegetation and soils taken within 5 km (the influenced area) of CNAAA. The thesis consists of an extensive review about the subject (part one) and of four papers (part two). The first paper is about the determination of {sup 14}C concentrations released by reactors (source strength). For Angra I, a device was developed in order to sample the gaseous effluents and for Angra II, a commercial monitoring system had already been implemented since its initial operation (2001). The {sup 14}C can be emitted as hydrocarbons, CO or CO{sub 2}, depending on the type of reactor. For PWRs, the main chemical form released is hydrocarbons (80 %). The monitoring system of Angra I was planned to determine both CO{sub 2} and hydrocarbon fractions but in Angra II, all hydrocarbons are converted to CO{sub 2} by using a Pd/Al{sub 2}O{sub 3} catalyst at 450 deg C. The liquid scintillation was the method employed to measure the samples. The second one concerns the atmospheric dispersion of the released

  2. Breath 14CO2 after intravenous administration of [14C]aminopyrine in liver diseases

    International Nuclear Information System (INIS)

    Pauwels, S.; Geubel, A.P.; Dive, C.; Beckers, C.

    1982-01-01

    The determination of of 14 CO2 in breath after oral administration of [ 14 C]aminopyrine has been proposed as a quantitative liver function test. In order to shorten the procedure and avoid misinterpretations related to variable rates of intestinal absorption, the [ 14 C]aminopyrine breath test (ABT) was performed after intravenous administration of [ 14 C]aminopyrine in 21 controls and 89 patients with biopsy-proven liver disease. The specific activity of the first hour sample corrected for body weight (SA1) was the most discriminant expression of breath data. The SA1 value, expressed as the percentage of the administered dose, was 0.86 +/- 0.1% (mean +/- SD) in controls and significantly less in patients (0.46 +/- 0.31%). Low values were observed in patients with untreated chronic active hepatitis (0.16 +/- 0.13%), alcoholic cirrhosis (0.2 +/ 0.15%0, and untreated postnecrotic cirrhosis (0.47 +/- 0.17%). In contrast, normal values were obtained in chronic persistent hepatitis (0.86 +/- 0.13%) and 58% of noncirrhotic alcoholic liver diseases (0.83 +/- 0.27%). The results of duplicate studies were reproducible and SA1 correlated with other conventional liver function tests, including 45-min BSP retention. Among these, ABT was the most sensitive screening test for the presence of cirrhosis, especially in alcoholic patients, where it allowed a sharp distinction between cirrhotic and noncirrhotic cases. The results obtained in chronic hepatitis suggested that ABT may provide a reliable index of the activity of the disease. In our hands, intravenous ABT, performed over a 1-hr period, was a fast, sensitive, and discriminant liver function test

  3. Metabolic patterns of 14C incorporation by selected vascular plants following field incubations with acetate-2-14C in two plant successional stages in Glacier Bay, Alaska

    International Nuclear Information System (INIS)

    Wu, Pei-Hsing Lin

    1975-01-01

    Metabolic patterns of some vascular plants (Dryas sp., Vaccinium sp., Salix sp., Alnus sp., Epilobium sp.), occurring in successional habitats, following acetate-2- 14 C incubations in the field were demonstrated for the first time. Relative radioactivity within the alcoholic soluble fraction of each species reflects its distribution in successional communities. A high level of 14 C-sugars was present in the plants of the pioneer community; on the other hand a high level of 14 C-organic acids was present in the plants of the forest community. Three patterns, based on the relative activities of the sugar- and organic acid-pools were noted which correspond to the range and the frequency of occurrence of each species in the successional stages. Only two types of 14 C-amino acid levels were noted corresponding to the range of distribution. Plants having less than 10% relative radioactivity in amino acid-pools had a limited range of distribution and reside in only one habitat; plants having more than 10% radioactivity showed wider ranges of distribution occurring in at least two habitats. (auth.)

  4. Synthesis of uniformly labelled organic compounds by polymerization of 14C ethylene

    International Nuclear Information System (INIS)

    Dauphin, J.-F.

    1972-01-01

    The synthesis of 14 C uniformly labelled compounds is described. By polymerization of 14 C ethylene, linear olefins with a double bond at α position were obtained. From these olefins, uniformly labelled alkanes, alcohols and acids were prepared [fr

  5. RECUPERACIÓN DE POLI-b-HIDROXIHEXANOATO- CO-OCTANOATO SINTETIZADO POR Pseudomonas putida MEDIANTE EL USO DE DISPERSIONES H I P O C LO R I TO - C LO RO F O R M O

    Directory of Open Access Journals (Sweden)

    A. Espinosa-Hernández

    2006-06-01

    Full Text Available Se estandarizó una técnica de recuperación de poli-3-hidroxihexanoato-co-hidroxioctanoato a partir de P. putida. El método emplea dispersiones de hipoclorito de sodio-cloroformo para la digestión delmaterial celular y solubilización del polímero, respectivamente. Se evaluó el efecto de la concentración de hipoclorito, la temperatura y el tiempo sobre el porcentaje de recuperación, pureza, peso molecular y temperatura de fusión. Las mejores condiciones para recuperar este polímero fueron: hipoclorito al 5.25% (p/v a 60°C durante 1 hora. Empleando estas condiciones fue posible mantener el peso molecularpor encima del 87% con respecto al obtenido mediante extracción con cloroformo. La temperatura de fusión del polímero fue 57.7°C y 56.4°C para dos muestras al azar. La pureza del material recuperado esde 96%.

  6. Bound residues in corn plants treated with 14C-atrazine and bioavailability to rats

    International Nuclear Information System (INIS)

    Khan, S.U.

    1986-01-01

    Corn plants, about 3.5 months old and treated with 14 C-atrazine, were used in an experiment in which the aerial portion of the plants was exhaustively extracted with solvents. The extracted dried material containing bound 14 C-residues was fed to rats. The extracted aerial portion of control corn plants fortified with 14 C-atrazine was also fed to rats. After four days, 88% and 32% of the radioactivity was excreted in the faeces, and 10% and 60% radioactivity was voided in the urine from rats fed plant material containing bound and fortified 14 C-residues, respectively. The data suggest that the bioavailability to rats of bound 14 C-residues in corn material is low. (author)

  7. Radioactive levels and doses of 3H and 14C in white spirits

    International Nuclear Information System (INIS)

    Deng, G.

    1992-01-01

    'Full Text:' White (and yeast) spirits is a general name for strong alcoholic beverages in China. The paper reports levels and doses of 3 H and 14 C in 65 spirits samples between 1986 and 1987. Experiments were made by measuring end analyzing each sample, using a low background liquid scintillation spectrometer. Radioactive levels of 65 spirits samples are as follows: Variant range of 3 H activity is 98.2 - 170.6Bq.dm -3 and its average is 149.2 ± 17.3Bq.dm -3 ; Variant range of 14 C activity is 38.8-80.2Bq.dm -3 and its average is 57.4±8.2Bq.dm -3 . If the man drinks 200cm 3 of spirits daily, the annual dose equivalents will be 0.19uSv of 3 H and 2.5uSv of 14 C . In ordinary strong alcoholic beverages that contain 57-60% alcohol, the mean 3 H and 14 C activities are 153.8Bq.dm -3 and 60.3Bq.dm -3 , respectively, but in spirits of lower alcoholic content (38-40%), the mean 3H activity is 114.6Bq.dm -3 , that is 25.5% less than ordinary spirits, and the mean 14 C activity is 46.1Bq.dm -3 , that is 23.5% less than ordinary spirits. We compared the 3 H and 14 C contents of five kinds of staple grains from both Sichuan and Guangdong provinces. We learned that the level of activity in spirits is ten times higher than in grains and water, and the level of 14 C activity in spirits is equivalent to that in grains. White spirits has fully concentrated 3 H and 14 C from both grain and water, and activities increase with increasing alcoholic content. 3 H in spirits probably is averaged from both water and grain, and 14 C is averaged mostly from grain. (author)

  8. Reassessment of the C-13/C-12 and C-14/C-12 isotopic fractionation ratio and its impact on high-precision radiocarbon dating

    NARCIS (Netherlands)

    Fahrni, Simon M.; Southon, John R.; Santos, Guaciara M.; Palstra, Sanne W. L.; Meijer, Harro A. J.; Xu, Xiaomei

    2017-01-01

    The vast majority of radiocarbon measurement results (C-14/C-12 isotopic ratios or sample activities) are corrected for isotopic fractionation processes (measured as C-13/C-12 isotopic ratios) that occur in nature, in sample preparation and measurement. In 1954 Harmon Craig suggested a value of 2.0

  9. Detergent Isolation Stabilizes and Activates the Shigella Type III Secretion System Translocator Protein IpaC.

    Science.gov (United States)

    Bernard, Abram R; Duarte, Shari M; Kumar, Prashant; Dickenson, Nicholas E

    2016-07-01

    Shigella rely on a type III secretion system as the primary virulence factor for invasion and colonization of human hosts. Although there are an estimated 90 million Shigella infections, annually responsible for more than 100,000 deaths worldwide, challenges isolating and stabilizing many type III secretion system proteins have prevented a full understanding of the Shigella invasion mechanism and additionally slowed progress toward a much needed Shigella vaccine. Here, we show that the non-denaturing zwitterionic detergent N, N-dimethyldodecylamine N-oxide (LDAO) and non-ionic detergent n-octyl-oligo-oxyethylene efficiently isolated the hydrophobic Shigella translocator protein IpaC from the co-purified IpaC/IpgC chaperone-bound complex. Both detergents resulted in monomeric IpaC that exhibits strong membrane binding and lysis characteristics while the chaperone-bound complex does not, suggesting that the stabilizing detergents provide a means of following IpaC "activation" in vitro. Additionally, biophysical characterization found that LDAO provides significant thermal and temporal stability to IpaC, protecting it for several days at room temperature and brief exposure to temperatures reaching 90°C. In summary, this work identified and characterized conditions that provide stable, membrane active IpaC, providing insight into key interactions with membranes and laying a strong foundation for future vaccine formulation studies taking advantage of the native immunogenicity of IpaC and the stability provided by LDAO. Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  10. Rapid analysis method for the determination of 14C specific activity in irradiated graphite.

    Science.gov (United States)

    Remeikis, Vidmantas; Lagzdina, Elena; Garbaras, Andrius; Gudelis, Arūnas; Garankin, Jevgenij; Plukienė, Rita; Juodis, Laurynas; Duškesas, Grigorijus; Lingis, Danielius; Abdulajev, Vladimir; Plukis, Artūras

    2018-01-01

    14C is one of the limiting radionuclides used in the categorization of radioactive graphite waste; this categorization is crucial in selecting the appropriate graphite treatment/disposal method. We propose a rapid analysis method for 14C specific activity determination in small graphite samples in the 1-100 μg range. The method applies an oxidation procedure to the sample, which extracts 14C from the different carbonaceous matrices in a controlled manner. Because this method enables fast online measurement and 14C specific activity evaluation, it can be especially useful for characterizing 14C in irradiated graphite when dismantling graphite moderator and reflector parts, or when sorting radioactive graphite waste from decommissioned nuclear power plants. The proposed rapid method is based on graphite combustion and the subsequent measurement of both CO2 and 14C, using a commercial elemental analyser and the semiconductor detector, respectively. The method was verified using the liquid scintillation counting (LSC) technique. The uncertainty of this rapid method is within the acceptable range for radioactive waste characterization purposes. The 14C specific activity determination procedure proposed in this study takes approximately ten minutes, comparing favorably to the more complicated and time consuming LSC method. This method can be potentially used to radiologically characterize radioactive waste or used in biomedical applications when dealing with the specific activity determination of 14C in the sample.

  11. Translocation and distribution of 14C-assimilation products in soybeans with different growth property

    International Nuclear Information System (INIS)

    Yoshida, Koichi; Gotoh, Kanji

    1975-01-01

    To 3 different kinds of soybeans, Tokachinagaha (Determinate), Koganejiro (Intermediate), and Harosoy (Indeterminate), 14 C was given at 3 stages of growth, namely, initial flowering, young pod development, and seed fattening periods. The 14 C assimilation efficiency, namely, the value of total 14 C assimilated divided by the area of the leaves which assimilated 14 C, was large when the leaf area was small. The value decreased with the increase of the leaf area. The rate of translocation of 14 C assimilation products was 20-50% in the period of initial flowering. The rate was highest in Tokachinagaha, followed by Koganejiro and Harosoy in this order. The difference was small in the period of young pod development. In the period of initial flowering, the distribution of 14 C to lower leaves and branches was high in Harosoy. In the period of young pod development, 30-40% of the assimilated 14 C was found in stems. This distribution is possibly due to temporary storage. In the period of seed fattening, 80-90% of the assimilated 14 C was present in pods and seeds. It was then concluded that the movement of assimilated products is high in the determinate type in the initial growth period. In the seed fattening period, the rate is high in the indeterminate type soy beans. (Fukutomi, T.)

  12. Rapid analysis method for the determination of 14C specific activity in irradiated graphite.

    Directory of Open Access Journals (Sweden)

    Vidmantas Remeikis

    Full Text Available 14C is one of the limiting radionuclides used in the categorization of radioactive graphite waste; this categorization is crucial in selecting the appropriate graphite treatment/disposal method. We propose a rapid analysis method for 14C specific activity determination in small graphite samples in the 1-100 μg range. The method applies an oxidation procedure to the sample, which extracts 14C from the different carbonaceous matrices in a controlled manner. Because this method enables fast online measurement and 14C specific activity evaluation, it can be especially useful for characterizing 14C in irradiated graphite when dismantling graphite moderator and reflector parts, or when sorting radioactive graphite waste from decommissioned nuclear power plants. The proposed rapid method is based on graphite combustion and the subsequent measurement of both CO2 and 14C, using a commercial elemental analyser and the semiconductor detector, respectively. The method was verified using the liquid scintillation counting (LSC technique. The uncertainty of this rapid method is within the acceptable range for radioactive waste characterization purposes. The 14C specific activity determination procedure proposed in this study takes approximately ten minutes, comparing favorably to the more complicated and time consuming LSC method. This method can be potentially used to radiologically characterize radioactive waste or used in biomedical applications when dealing with the specific activity determination of 14C in the sample.

  13. Metabolism of [2-14C]acetate and its use in assessing hepatic Krebs cycle activity and gluconeogenesis

    International Nuclear Information System (INIS)

    Schumann, W.C.; Magnusson, I.; Chandramouli, V.; Kumaran, K.; Wahren, J.; Landau, B.R.

    1991-01-01

    To examine the fate of the carbons of acetate and to evaluate the usefulness of labeled acetate in assessing intrahepatic metabolic processes during gluconeogenesis, [2-14C]acetate, [2-14C]ethanol, and [1-14C]ethanol were infused into normal subjects fasted 60 h and given phenyl acetate. Distributions of 14C in the carbons of blood glucose and glutamate from urinary phenylacetylglutamine were determined. With [2-14C]acetate and [2-14C]ethanol, carbon 1 of glucose had about twice as much 14C as carbon 3. Carbon 2 of glutamate had about twice as much 14C as carbon 1 and one-half to one-third as much as carbon 4. There was only a small amount in carbon 5. These distributions are incompatible with the metabolism of [2-14C]acetate being primarily in liver. Therefore, [2-14C]acetate cannot be used to study Krebs cycle metabolism in liver and in relationship to gluconeogenesis, as has been done. The distributions can be explained by: (a) fixation of 14CO2 from [2-14C]acetate in the formation of the 14C-labeled glucose and glutamate in liver and (b) the formation of 14C-labeled glutamate in a second site, proposed to be muscle. [1,3-14C]Acetone formation from the [2-14C]acetate does not contribute to the distributions, as evidenced by the absence of 14C in carbons 2-4 of glutamate after [1-14C]ethanol administration

  14. The study of variations and environmental applications 14C

    International Nuclear Information System (INIS)

    Simon, J.

    2010-01-01

    The primary aim of the presented thesis is to explain experimentally observed 14 C variations in the outer atmosphere. Physical models have been developed to quantify directly immeasurable phenomena relevant in the field of radiocarbon dynamics. Namely atmospheric stability, 14 C transport from the stratosphere to the lower troposphere and fossil carbon dioxide emissions to the atmosphere. Finally these models have been used as the pillars of the united theory of Δ 14 C dynamics. Besides the presented main theoretical outputs, this thesis also provides couple of potentially implementable by-products. First of them is a method to evaluate so called 'equivalent mixing height' and turbulent diffusion coefficient using temporal changes of 222 Rn concentration in the boundary layer of the atmosphere. The elaborated mathematical apparatus for the evaluation of aerosol scavenging by raindrops can be utilized in the models of pollutant dispersion. Information on turbulent diffusion coefficient at higher atmospheric levels is important for the models of stratospheric and ozonospheric dynamics. Nowadays, when one can measure and even feel the greenhouse effect consequences, the importance of an independent method for carbon dioxide fossil emissions assessment is obvious. Besides theoretical outcome, the thesis also presents experimental results. A network of CO 2 sampling sites has been established in Bratislava and the outskirts in the vicinity of the town. Together with mountain site Chopok the network brought a unique information on 14 C distribution. Atmospheric measurements of 7 Be and 222 Rn activity are also presented here. Finally the PC codes have been developed to bridge a gap between experimental and theoretical results. (author)

  15. Cr(III), Fe(III) and Co(III) complexes of tetradentate (ONNO) Schiff base ligands: Synthesis, characterization, properties and biological activity

    Science.gov (United States)

    Keskioğlu, Eren; Gündüzalp, Ayla Balaban; Çete, Servet; Hamurcu, Fatma; Erk, Birgül

    2008-08-01

    A series of metal complexes were synthesized from equimolar amounts of Schiff bases: 1,4-bis[3-(2-hydroxy-1-naphthaldimine)propyl]piperazine (bappnaf) and 1,8-bis[3-(2-hydroxy-1-naphthaldimine)- p-menthane (damnaf) with metal chlorides. All of synthesized compounds were characterized by elemental analyses, spectral (UV-vis, IR, 1H- 13C NMR, LC-MS) and thermal (TGA-DTA) methods, magnetic and conductance measurements. Schiff base complexes supposed in tetragonal geometry have the general formula [M(bappnaf or damnaf)]Cl· nH 2O, where M = Cr(III), Co(III) and n = 2, 3. But also Fe(III) complexes have octahedral geometry by the coordination of two water molecules and the formula is [Fe(bappnaf or damnaf)(H 2O) 2]Cl. The changes in the selected vibration bands in FT-IR indicate that Schiff bases behave as (ONNO) tetradentate ligands and coordinate to metal ions from two phenolic oxygen atoms and two azomethine nitrogen atoms. Conductance measurements suggest 1:1 electrolytic nature of the metal complexes. The synthesized compounds except bappnaf ligand have the antimicrobial activity against the bacteria: Escherichia coli (ATCC 11230), Yersinia enterocolitica (ATCC 1501), Bacillus magaterium (RSKK 5117), Bacillus subtilis (RSKK 244), Bacillus cereus (RSKK 863) and the fungi: Candida albicans (ATCC 10239). These results have been considerably interest in piperazine derivatives due to their significant applications in antimicrobial studies.

  16. The distribution of Δ{sup 14}C in Korea from 2010 to 2013

    Energy Technology Data Exchange (ETDEWEB)

    Park, J.H., E-mail: junghun@kigam.re.kr [Korea Institute of Geoscience and Mineral Resources (KIGAM), 124 Gwahang-no. Yuseong, Daejeon 305-350 (Korea, Republic of); Hong, W. [Korea Institute of Geoscience and Mineral Resources (KIGAM), 124 Gwahang-no. Yuseong, Daejeon 305-350 (Korea, Republic of); Xu, X. [Keck/CCAMS Lab, 3327 Croul Hall, University of California, Irvine, CA 92697 (United States); Park, G.; Sung, K.S.; Sung, Kilho; Lee, Jong-geol; Nakanishi, T.; Park, Hyo-Seok [Korea Institute of Geoscience and Mineral Resources (KIGAM), 124 Gwahang-no. Yuseong, Daejeon 305-350 (Korea, Republic of)

    2015-10-15

    Δ{sup 14}C values of leaves of a deciduous tree record to those of atmospheric CO{sub 2} within error and were used to map out Δ{sup 14}C distribution in Korea. We collected ginkgo (Ginkgo biloba Linnaeus, a deciduous tree) leaf samples in mid-June to early July from 2009 to 2013 in Korea to obtain the regional distribution of Δ{sup 14}C. Commonly CO{sub 2} emitted from fossil fuel consumption dilutes atmospheric {sup 14}C, while operations and accidents at nuclear power plants can increase it. The distribution maps of Δ{sup 14}C from 2010 to 2013 in Korea shows that Δ{sup 14}C values in the northwestern and southeastern parts of Korea are lower than those of the other parts of Korea, which is consistent with the population and industry patterns. Decrease rates of annually averaged Δ{sup 14}C values in Korea over the study period are larger than those of Pt. Barrow, Alaska, USA (71.3°N, 156.5°W), so the difference between them and those of Pt. Barrow, Alaska, USA became larger annually. This may be due to the increase in fossil fuel consumption in Korea and China. The decrease rate between 2010 and 2011 was smaller than in other years. This could be the effect of the Fukushima power plant accident which occurred in March 11, 2011, but further study is needed to clarify it.

  17. Amo 1618 effects on incorporation of 14C-MVA and 14C-acetate into sterols in Nicotiana and Digitalis seedlings and cell-free preparations from Nicotiana

    International Nuclear Information System (INIS)

    Douglas, T.J.; Paleg, L.G.

    1978-01-01

    Incorporation of radioactivity from acetate-[ 14 C] and MVA-[ 14 C] into sterols and sterol precursors in tobacco was inhibited by Amo 1618; differing patterns of accumulation were obtained with the two precursors, suggesting more than one point of inhibition. This was borne out with cell-free preparations with which it was demonstrated that both HMG-CoA reductase and squalene-2,3-epoxide cyclase were inhibited, the latter more strongly than the former. GLC analysis of gross sterol and hydrocarbon fractions confirmed previous indications that incorporation of radioactivity into individual sterols was inhibited by Amo 1618. Finally, incorporation of MVA-[ 14 C] into sterols and sterol precursors of Digitalis was significantly altered by the retardant, thus expanding the generality of the relationship between sterol (particularly 4-desmethylsterol) biosynthesis inhibition and retardant effect. (author)

  18. Dynamics of 14C-labeled glucose and ammonium in saline arable soils

    International Nuclear Information System (INIS)

    Vuelvas-Solorzano, Alma; Hernandez-Matehuala, Rosalina; Conde-Barajas, Eloy; Cardenas-Manriquez, Marcela; Luna-Guido, Marco L.; Dendooven, Luc

    2009-01-01

    Organic matter dynamics and nutrient availability in saline agricultural soils of the State of Guanajuato might provide information for remediation strategies. 14 C labeled glucose with or without 200 mg kg - 1 of NH 4 + -N soil was added to two clayey agricultural soils with different electrolytic conductivity (EC), i.e. 0.94 dS m - 1 (low EC; LEC) and 6.72 dS m - 1 (high EC; HEC), to investigate the effect of N availability and salt content on organic material decomposition. Inorganic N dynamics and production of CO 2 and 14 CO 2 were monitored. Approximately 60 % of the glucose- 14 C added to LEC soil evolved as 14 CO 2 , but only 20 % in HEC soil after the incubation period of 21 days. After one day, 14 C was extractable from LEC soil, but > 500 mg 14 C from HEC soil. No N mineralization occurred in the LEC and HEC soils and glucose addition reduced the concentrations of inorganic N in unamended soil and soil amended with NH 4 + -N. The NO 2 - and NO 3 - concentrations were on average higher in LEC than in HEC soil, with exception of NO 2 - in HEC amended with NH 4 + -N. It was concluded that increases in soil EC reduced mineralization of the easily decomposable C substrate and resulted in N-depleted soil. (author)

  19. In vitro incorporation of (U-C/sup 14/)-glucose and (1-C/sup