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Sample records for carbon 11

  1. The 11 Micron Emissions of Carbon Stars

    NASA Technical Reports Server (NTRS)

    Goebel, J. H.; Cheeseman, P.; Gerbault, F.

    1995-01-01

    A new classification scheme of the IRAS LRS carbon stars is presented. It comprises the separation of 718 probable carbon stars into 12 distinct self-similar spectral groupings. Continuum temperatures are assigned and range from 470 to 5000 K. Three distinct dust species are identifiable: SiC, alpha:C-H, and MgS. In addition to the narrow 11 + micron emission feature that is commonly attributed to SiC, a broad 11 + micron emission feature, that is correlated with the 8.5 and 7.7 micron features, is found and attributed to alpha:C-H. SiC and alpha:C-H band strengths are found to correlate with the temperature progression among the Classes. We find a spectral sequence of Classes that reflects the carbon star evolutionary sequence of spectral types, or alternatively developmental sequences of grain condensation in carbon-rich circumstellar shells. If decreasing temperature corresponds to increasing evolution, then decreasing temperature corresponds to increasing C/O resulting in increasing amounts of carbon rich dust, namely alpha:C-H. If decreasing the temperature corresponds to a grain condensation sequence, then heterogeneous, or induced nucleation scenarios are supported. SiC grains precede alpha:C-H and form the nuclei for the condensation of the latter material. At still lower temperatures, MgS appears to be quite prevalent. No 11.3 micron PAH features are identified in any of the 718 carbon stars. However, one of the coldest objects, IRAS 15048-5702, and a few others, displays an 11.9 micron emission feature characteristic of laboratory samples of coronene. That feature corresponds to the C-H out of plane deformation mode of aromatic hydrocarbon. This band indicates the presence of unsaturated, sp(sup 3), hydrocarbon bonds that may subsequently evolve into saturated bonds, sp(sup 2), if, and when, the star enters the planetary nebulae phase of stellar evolution. The effusion of hydrogen from the hydrocarbon grain results in the evolution in wavelength of this

  2. 46 CFR 97.37-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 4 2014-10-01 2014-10-01 false Carbon dioxide warning signs. 97.37-11 Section 97.37-11... OPERATIONS Markings for Fire and Emergency Equipment, Etc. § 97.37-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or...

  3. 46 CFR 97.37-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 4 2012-10-01 2012-10-01 false Carbon dioxide warning signs. 97.37-11 Section 97.37-11... OPERATIONS Markings for Fire and Emergency Equipment, Etc. § 97.37-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or...

  4. 46 CFR 78.47-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 3 2012-10-01 2012-10-01 false Carbon dioxide warning signs. 78.47-11 Section 78.47-11... Fire and Emergency Equipment, Etc. § 78.47-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or any space into...

  5. 46 CFR 78.47-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 3 2014-10-01 2014-10-01 false Carbon dioxide warning signs. 78.47-11 Section 78.47-11... Fire and Emergency Equipment, Etc. § 78.47-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or any space into...

  6. 46 CFR 78.47-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 3 2013-10-01 2013-10-01 false Carbon dioxide warning signs. 78.47-11 Section 78.47-11... Fire and Emergency Equipment, Etc. § 78.47-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or any space into...

  7. 46 CFR 97.37-11 - Carbon dioxide warning signs.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 4 2013-10-01 2013-10-01 false Carbon dioxide warning signs. 97.37-11 Section 97.37-11... OPERATIONS Markings for Fire and Emergency Equipment, Etc. § 97.37-11 Carbon dioxide warning signs. Each entrance to a space storing carbon dioxide cylinders, a space protected by carbon dioxide systems, or...

  8. Carbon-11: Where Familiar Chemistry Still Holds New Challenges.

    ERIC Educational Resources Information Center

    Feliu, Anthony L.

    1990-01-01

    Discussed are the properties, chemistry, generation of precursors, and use in organic synthesis of this isotope of carbon. The use of carbon-11 in research is emphasized. Pitfalls and possibilities are described. (CW)

  9. One carbon metabolism in SAR11 pelagic marine bacteria.

    PubMed

    Sun, Jing; Steindler, Laura; Thrash, J Cameron; Halsey, Kimberly H; Smith, Daniel P; Carter, Amy E; Landry, Zachary C; Giovannoni, Stephen J

    2011-01-01

    The SAR11 Alphaproteobacteria are the most abundant heterotrophs in the oceans and are believed to play a major role in mineralizing marine dissolved organic carbon. Their genomes are among the smallest known for free-living heterotrophic cells, raising questions about how they successfully utilize complex organic matter with a limited metabolic repertoire. Here we show that conserved genes in SAR11 subgroup Ia (Candidatus Pelagibacter ubique) genomes encode pathways for the oxidation of a variety of one-carbon compounds and methyl functional groups from methylated compounds. These pathways were predicted to produce energy by tetrahydrofolate (THF)-mediated oxidation, but not to support the net assimilation of biomass from C1 compounds. Measurements of cellular ATP content and the oxidation of (14)C-labeled compounds to (14)CO(2) indicated that methanol, formaldehyde, methylamine, and methyl groups from glycine betaine (GBT), trimethylamine (TMA), trimethylamine N-oxide (TMAO), and dimethylsulfoniopropionate (DMSP) were oxidized by axenic cultures of the SAR11 strain Ca. P. ubique HTCC1062. Analyses of metagenomic data showed that genes for C1 metabolism occur at a high frequency in natural SAR11 populations. In short term incubations, natural communities of Sargasso Sea microbial plankton expressed a potential for the oxidation of (14)C-labeled formate, formaldehyde, methanol and TMAO that was similar to cultured SAR11 cells and, like cultured SAR11 cells, incorporated a much larger percentage of pyruvate and glucose (27-35%) than of C1 compounds (2-6%) into biomass. Collectively, these genomic, cellular and environmental data show a surprising capacity for demethylation and C1 oxidation in SAR11 cultures and in natural microbial communities dominated by SAR11, and support the conclusion that C1 oxidation might be a significant conduit by which dissolved organic carbon is recycled to CO(2) in the upper ocean. PMID:21886845

  10. Ethanolic carbon-11 chemistry: the introduction of green radiochemistry.

    PubMed

    Shao, Xia; Fawaz, Maria V; Jang, Keunsam; Scott, Peter J H

    2014-07-01

    The principles of green chemistry have been applied to a radiochemistry setting. Eleven carbon-11 labeled radiopharmaceuticals have been prepared using ethanol as the only organic solvent throughout the entire manufacturing process. The removal of all other organic solvents from the process simplifies production and quality control (QC) testing, moving our PET Center towards the first example of a green radiochemistry laboratory. All radiopharmaceutical doses prepared are suitable for clinical use. PMID:24631743

  11. Ethanolic Carbon-11 Chemistry: the Introduction of Green Radiochemistry

    PubMed Central

    Shao, Xia; Fawaz, Maria V.; Jang, Keunsam; Scott, Peter J. H.

    2014-01-01

    The principles of green chemistry have been applied to a radiochemistry setting. Eleven carbon-11 labeled radiopharmaceuticals have been prepared using ethanol as the only organic solvent throughout the entire manufacturing process. The removal of all other organic solvents from the process simplifies production and quality control (QC) testing, moving our PET Center towards the first example of a green radiochemistry laboratory. All radiopharmaceutical doses prepared are suitable for clinical use. PMID:24631743

  12. Ethanolic carbon-11 chemistry: the introduction of green radiochemistry.

    PubMed

    Shao, Xia; Fawaz, Maria V; Jang, Keunsam; Scott, Peter J H

    2014-07-01

    The principles of green chemistry have been applied to a radiochemistry setting. Eleven carbon-11 labeled radiopharmaceuticals have been prepared using ethanol as the only organic solvent throughout the entire manufacturing process. The removal of all other organic solvents from the process simplifies production and quality control (QC) testing, moving our PET Center towards the first example of a green radiochemistry laboratory. All radiopharmaceutical doses prepared are suitable for clinical use.

  13. The 11 micron Silicon Carbide Feature in Carbon Star Shells

    NASA Technical Reports Server (NTRS)

    Speck, A. K.; Barlow, M. J.; Skinner, C. J.

    1996-01-01

    Silicon carbide (SiC) is known to form in circumstellar shells around carbon stars. SiC can come in two basic types - hexagonal alpha-SiC or cubic beta-SiC. Laboratory studies have shown that both types of SiC exhibit an emission feature in the 11-11.5 micron region, the size and shape of the feature varying with type, size and shape of the SiC grains. Such a feature can be seen in the spectra of carbon stars. Silicon carbide grains have also been found in meteorites. The aim of the current work is to identity the type(s) of SiC found in circumstellar shells and how they might relate to meteoritic SiC samples. We have used the CGS3 spectrometer at the 3.8 m UKIRT to obtain 7.5-13.5 micron spectra of 31 definite or proposed carbon stars. After flux-calibration, each spectrum was fitted using a chi(exp 2)-minimisation routine equipped with the published laboratory optical constants of six different samples of small SiC particles, together with the ability to fit the underlying continuum using a range of grain emissivity laws. It was found that the majority of observed SiC emission features could only be fitted by alpha-SiC grains. The lack of beta-SiC is surprising, as this is the form most commonly found in meteorites. Included in the sample were four sources, all of which have been proposed to be carbon stars, that appear to show the SiC feature in absorption.

  14. Delineation of myocardial oxygen utilization with carbon-11-labeled acetate

    SciTech Connect

    Brown, M.; Marshall, D.R.; Sobel, B.E.; Bergmann, S.R.

    1987-09-01

    Although positron-emission tomography (PET) with labeled fatty acid delineates infarct size and permits qualitative assessment of fatty acid utilization, quantification of oxidative metabolism is limited by complex alterations in the pattern of utilization of fatty acid during ischemia and reperfusion. Because metabolism of acetate by myocardium is less complex than that of glucose or palmitate, we characterized kinetics of utilization of radiolabeled acetate in 37 isolated rabbit hearts perfused with modified Krebs-Henseleit buffer and performed a pilot tomographic study in man. Results of initial experiments with carbon-14-labeled acetate (/sup 14/C-acetate) indicated that the steady-state extraction fraction of acetate averaged 61.5 +/- 4.0% in control hearts (n = 4), 93.6 +/- 0.9% in hearts rendered ischemic (n = 4), and 54.8 +/- 4.0% in hearts reperfused after 60 min of ischemia (n = 3). Oxidation of /sup 14/C-acetate, assessed from the rate of efflux of /sup 14/CO/sub 2/ in the venous effluent, correlated closely with the rate of oxygen consumption under diverse metabolic conditions (r = .97, p less than .001). In addition, no significant differences were observed between rates of efflux of total /sup 14/C in all chemical species (reflecting total clearance of tracer from myocardium) and efflux of /sup 14/CO/sub 2/. Clearance of /sup 11/C-acetate, measured externally with gamma probes in normal and ischemic myocardium, correlated closely with clearance of /sup 14/C-acetate measured directly in the effluent (r = .99, p less than .001) and with overall myocardial oxygen consumption (r = .95, p less than .001). Accumulation and clearance of /sup 11/C-acetate from human myocardium with PET demonstrated kinetics comparable to those seen with radiolabeled acetate in vitro.

  15. Noninvasive measurement of lung carbon-11-serotonin extraction in man

    SciTech Connect

    Coates, G.; Firnau, G.; Meyer, G.J.; Gratz, K.F. )

    1991-04-01

    The fraction of serotonin extracted on a single passage through the lungs is being used as an early indicator of lung endothelial damage but the existing techniques require multiple arterial blood samples. We have developed a noninvasive technique to measure lung serotonin uptake in man. We utilized the double indicator diffusion principle, a positron camera, {sup 11}C-serotonin as the substrate, and {sup 11}CO-erythrocytes as the vascular marker. From regions of interest around each lung, we recorded time-activity curves in 0.5-sec frames for 30 sec after a bolus injection of first the vascular marker {sup 11}CO-erythrocytes and 10 min later {sup 11}C-serotonin. A second uptake measurement was made after imipramine 25-35 mg was infused intravenously. In three normal volunteers, the single-pass uptake of {sup 11}C-serotonin was 63.9% +/- 3.6%. This decreased in all subjects to a mean of 53.6% +/- 1.4% after imipramine. The rate of lung washout of {sup 11}C was also significantly prolonged after imipramine. This noninvasive technique can be used to measure lung serotonin uptake to detect early changes in a variety of conditions that alter the integrity of the pulmonary endothelium.

  16. Synthesis and electrochemical capacitive properties of nitrogen-doped porous carbon micropolyhedra by direct carbonization of zeolitic imidazolate framework-11

    SciTech Connect

    Hao, Fei; Li, Li; Zhang, Xiaohua Chen, Jinhua

    2015-06-15

    Highlights: • Nitrogen-doped porous carbon micropolyhedra (N-PCMPs) were prepared from ZIF-11. • The activated N-PCMPs with fused KOH (N-PCMPs-A) have high specific surface area. • N-PCMPs-A exhibits high specific capacitance. • N-PCMPs-A reveals good cycling performance even at a high current density. - Abstract: Nitrogen-doped porous carbon micropolyhedra (N-PCMPs) were successfully prepared by direct carbonization of ZIF-11 polyhedra and further activated with fused KOH to obtain N-PCMPs-A. The morphology and microstructure of samples were examined by scanning electron microscopy, X-ray diffraction, and micropore and chemisorption analyzer. Electrochemical properties were characterized by cyclic voltammetry and galvanostatic charge/discharge method in 1.0 M H{sub 2}SO{sub 4} aqueous solution on a standard three-electrode system. Results show that, compared with N-PCMPs, N-PCMPs-A has higher specific surface area (2188 m{sup 2} g{sup −1}) and exhibits improved electrochemical capacitive properties (307 F g{sup −1} at 1.0 A g{sup −1}). The mass specific capacitance of N-PCMPs-A is also higher than that of most MOF-derived carbons, some carbide-derived carbons and carbon aerogel-derived carbons. In addition, the capacitance of the N-PCMPs-A retains 90% after 4000 cycles even at a high current density of 10 A g{sup −1}. These imply that N-PCMPs-A is the promising materials for the construction of a high-performance supercapacitor.

  17. Diffusion of 1,1-dimethylethyl-benzene (1); carbon dioxide (2)

    NASA Astrophysics Data System (ADS)

    Winkelmann, J.

    This document is part of Subvolume A `Gases in Gases, Liquids and their Mixtures' of Volume 15 `Diffusion in Gases, Liquids and Electrolytes' of Landolt-Börnstein Group IV `Physical Chemistry'. It is part of the chapter of the chapter `Diffusion in Pure Gases' and contains data on diffusion of (1) 1,1-dimethylethyl-benzene; (2) carbon dioxide

  18. Diffusion of cis-5,8,11,14,17-eicosapentaenoic acid (1); carbon dioxide (2)

    NASA Astrophysics Data System (ADS)

    Winkelmann, J.

    This document is part of Subvolume A `Gases in Gases, Liquids and their Mixtures' of Volume 15 `Diffusion in Gases, Liquids and Electrolytes' of Landolt-Börnstein Group IV `Physical Chemistry'. It is part of the chapter of the chapter `Diffusion in Pure Gases' and contains data on diffusion of (1) cis-5,8,11,14,17-eicosapentaenoic acid; (2) carbon dioxide

  19. Carbon 11-MPTP: a potential tracer for Parkinson's disease research in laboratory animals

    SciTech Connect

    Livni, E.; Spellman, J.P.; Correia, J.A.; Alpert, N.M.; Brownell, G.L.; Strauss, H.W.; Elmaleh, D.R.

    1986-10-01

    (11C)-1-Methyl-4-phenyl-1,2,5,6-tetrahydropyridine ((11C)MPTP), a compound producing parkinson-like symptoms in several species, has been synthesized and purified in sufficient activity to obtain tomographic images in the monkey. Biodistribution data has also been obtained in rats. Carbon-11-labeled MPTP could be used as a probe to study the pharmacokinetics of the compound under various research conditions in animals. Because of its neurotoxicity, the compound is not intended for use in humans.

  20. Synthesis of carbon-11, fluorine-18, and nitrogen-13 labeled radiotracers for biomedical applications

    SciTech Connect

    Fowler, J.S.; Wolf, A.P.

    1981-01-01

    A number of reviews, many of them recent, have appeared on various aspects of /sup 11/C, /sup 18/F and /sup 13/N-labeled radiotracers. This monograph treats the topic principally from the standpoint of synthetic organic chemistry while keeping in perspective the necessity of integrating the organic chemistry with the design and ultimate application of the radiotracer. Where possible, recent examples from the literature of organic synthesis are introduced to suggest potentially new routes which may be applied to problems in labeling organic molecules with the short-lived positron emitters, carbon-11, fluorine-18, and nitrogen-13. The literature survey of carbon-11, fluorine-18 and nitrogen-13 labeled compounds presented are of particular value to scientists working in this field. Two appendices are also included to provide supplementary general references. A subject index concludes this volume.

  1. Myocardial kinetics of carbon-11-epinephrine in the isolated working rat heart

    SciTech Connect

    Nguyen, N.T.B.; DeGrado, T.R.; Chakraborty, P.

    1997-05-01

    The kinetics of EPI were studied in the isolated rat heart model to evaluate {sup 11}C-epinephrine (EPI) as a radiotracer for the assessment of sympathetic neuronal function in the heart. Isolated rat hearts were perfused in a working mode. Carbon-11-EPI was added to the perfusate during wash-in period of 20 min, followed by a washout period of 40 min. Radioactivity in the heart was externally monitored and time-activity curves were recorded as a function of time. Effluent samples were collected throughout each study to determine the fraction of {sup 11}C radioactivity as intact tracer. Time-activity curves of control hearts showed that {sup 11}C-EPI is taken up and retained by the myocardium. Desipramine inhibition (DMI) of uptake-1 resulted in a significant decrease in myocardial uptake and retention of {sup 11}C-EPI by 91% compared to controls. Addition of DMI to the perfusion medium during washout did not affect kinetics of {sup 11}C-EPI compared to control hearts. Reserpine pretreated rat hearts also showed significant decrease in tracer retention of 95% compared to controls. The metabolic data showed that, in control conditions, about 61% of {sup 11}C-EPI taken up by the rat heart is rapidly metabolized and released. Carbon-11-EPI traces sympathetic nerve terminals in the isolated rat heart. Uptake blockade by DMI and reserpine suggest that uptake and storage of {sup 11}C-EPI appear to be similar to that of norepinephrine. However, the prominent metabolic pathway warrants further consideration. These results suggest that {sup 11}C-EPI may be a suitable radiolabeled tracer for the evaluation of sympathetic vesicular function of the heart by PET. 23 refs., 3 figs., 3 tabs.

  2. Development of a series of novel carbon-11 labeled PDE10A inhibitors.

    PubMed

    Stepanov, Vladimir; Miura, Shotaro; Takano, Akihiro; Amini, Nahid; Nakao, Ryuji; Hasui, Tomoaki; Nakashima, Kosuke; Taniguchi, Takahiko; Kimura, Haruhide; Kuroita, Takanobu; Halldin, Christer

    2015-05-15

    Phosphodiesterase 10A (PDE10A) is a member of the PDE family of enzymes that degrades cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP). Our aim was to label a series of structurally related PDE10A inhibitors with carbon-11 and evaluate them as potential positron emission tomography (PET) radioligands for PDE10A using nonhuman primates. The series consisted of seven compounds based on the 3-(1H-pyrazol-5-yl)pyridazin-4(1H)-one backbone. These compounds were selected from the initial larger library based on a number of parameters such as affinity, selectivity for hPDE10A in in vitro tests, lipophilicity, and on the results of multidrug resistance protein 1 (MDR1)-LLCPK1 and the parallel artificial membrane permeability assays. Seven radioligands (KIT-1, 3, 5, 6, 7, 9, and 12) were radiolabeled with carbon-11 employing O-methylation on the hydroxyl moiety using [(11)C]methyl triflate. In vivo examination of each radioligand was performed using PET in rhesus monkeys; analysis of radiometabolites in plasma also was conducted using HPLC. All seven radioligands were labeled with high (>90%) incorporation of [(11)C]methyl triflate into their appropriate precursors and with high specific radioactivity. Carbon-11 labeled KIT-5 and KIT-6 showed high accumulation in the striatum, consistent with the known anatomical distribution of PDE10A in brain, accompanied by fast washout and high specific binding ratio. In particular [(11)C]KIT-6, named [(11)C]T-773, is a promising PET tool for further examination of PDE10A in human brain. PMID:25891816

  3. Carbon-carbon bond activation by 1,1-carboboration of internal alkynes.

    PubMed

    Chen, Chao; Kehr, Gerald; Fröhlich, Roland; Erker, Gerhard

    2010-10-01

    Internal alkynes undergo 1,1-carboboration reactions upon treatment with boranes RB(C(6)F(5))(2) (R = C(6)F(5), CH(3)) to yield trisubstituted alkenylboranes. These products can be used as substrates in Pd-catalyzed cross-coupling reactions. PMID:20831196

  4. Carbon-11 radiolabeling of iron-oxide nanoparticles for dual-modality PET/MR imaging

    NASA Astrophysics Data System (ADS)

    Sharma, Ramesh; Xu, Youwen; Kim, Sung Won; Schueller, Michael J.; Alexoff, David; Smith, S. David; Wang, Wei; Schlyer, David

    2013-07-01

    Dual-modality imaging, using Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET) simultaneously, is a powerful tool to gain valuable information correlating structure with function in biomedicine. The advantage of this dual approach is that the strengths of one modality can balance the weaknesses of the other. However, success of this technique requires developing imaging probes suitable for both. Here, we report on the development of a nanoparticle labeling procedure via covalent bonding with carbon-11 PET isotope. Carbon-11 in the form of [11C]methyl iodide was used as a methylation agent to react with carboxylic acid (-COOH) and amine (-NH2) functional groups of ligands bound to the nanoparticles (NPs). The surface coating ligands present on superparamagnetic iron-oxide nanoparticles (SPIO NPs) were radiolabeled to achieve dual-modality PET/MR imaging capabilities. The proof-of-concept dual-modality PET/MR imaging using the radiolabeled SPIO NPs was demonstrated in an in vivo experiment.Dual-modality imaging, using Magnetic Resonance Imaging (MRI) and Positron Emission Tomography (PET) simultaneously, is a powerful tool to gain valuable information correlating structure with function in biomedicine. The advantage of this dual approach is that the strengths of one modality can balance the weaknesses of the other. However, success of this technique requires developing imaging probes suitable for both. Here, we report on the development of a nanoparticle labeling procedure via covalent bonding with carbon-11 PET isotope. Carbon-11 in the form of [11C]methyl iodide was used as a methylation agent to react with carboxylic acid (-COOH) and amine (-NH2) functional groups of ligands bound to the nanoparticles (NPs). The surface coating ligands present on superparamagnetic iron-oxide nanoparticles (SPIO NPs) were radiolabeled to achieve dual-modality PET/MR imaging capabilities. The proof-of-concept dual-modality PET/MR imaging using the radiolabeled

  5. Assessment of dopamine receptor densities in the human brain with carbon-11-labeled N-methylspiperone

    SciTech Connect

    Wagner, H.N. Jr.; Burns, H.D.; Dannals, R.F.; Wong, D.F.; Langstroem, B.; Duelfer, T.; Frost, J.J.; Ravert, H.T.; Links, J.M.; Rosenbloom, S.B.

    1984-01-01

    We describe the use of carbon-11-labeled 3-N-methylspiperone, a ligand that preferentially binds to dopamine receptors in vivo, to image the receptors by positron emission tomography scanning in baboons and, for the first time, in a human. The method has now been used in 58 humans for noninvasive assessment of the state of brain dopamine receptors under normal and pathological conditions.

  6. Effects of active chronic cocaine use on cardiac sympathetic neuronal function assessed by carbon-11-hydroxyephedrine

    SciTech Connect

    Melon, P.G.; Boyd, C.J.; McVey, S. |

    1997-03-01

    Cardiac toxicity of cocaine has been linked to its inhibitory effect on norepinephrine reuptake by sympathetic nerve terminals of the heart. Carbon-11-hydroxyephedrine is a positron-emitting tracer that has been validated as a highly specific marker for norepinephrine transporter activity of the sympathetic nerve terminals and thus makes possible in vivo assessment of the effect of cocaine on norepinephrine reuptake and storage in the cardiac sympathetic nerve terminals. The aim of the study was to use the catecholamine analog {sup 11}C-hydroxyephedrine with PET to determine whether active chronic use of cocaine in women modifies the function of sympathetic nerve terminals of the heart. Six normal female volunteers and nine female active chronic cocaine users were studied. Cardiac regional {sup 11}C-hydroxyephedrine uptake and blood flow, as assessed with {sup 13}N-ammonia, were determined using semi-quantitative polar map analysis of myocardial tracer distribution. Carbon-11-hydroxyephedrine cardiac retention was quantified using dynamic data acquisition and kinetic analysis of blood and tissue activity. 27 refs., 4 figs., 3 tabs.

  7. Survey of lunar carbon compounds. I - The presence of indigenous gases and hydrolysable carbon compounds in Apollo 11 and Apollo 12 samples

    NASA Technical Reports Server (NTRS)

    Abell, P. I.; Cadogan, P. H.; Eglinton, G.; Maxwell, J. R.; Pillinger, C. T.

    1971-01-01

    Indigenous gases and hydrolyzable carbon compounds in Apollo 11 and 12 samples through gas chromatographic and mass spectrometric examination, noting meteoritic impact and solar wind implantation as probable origins

  8. [(11) C]Carbon monoxide in labeling chemistry and positron emission tomography tracer development: scope and limitations.

    PubMed

    Rahman, Obaidur

    2015-03-01

    [(11) C]Carbon monoxide is an attractive precursor for labeling carbonyl position in a wide range of organic compounds. The use of [(11) C]carbon monoxide in transition metal-mediated coupling reactions has been explored by several groups during the last 15 years, and an impressive number of the synthesis of [carbonyl-(11) C]compounds have been published to date. The application of radical-mediated [(11) C]carbonylation has also been explored in some extent. However, the main limitations to apply this potential precursor in (11) C-labeling chemistry are low concentration, poor solubility in commonly used organic solvents, and low reactivity. A couple of technical solutions such as high-pressure reactor system, microfluidic system, and different approaches to confine [(11) C]CO to the reaction media at ambient pressure have been developed over the years. Although considerable advances in [(11) C]carbon monoxide chemistry have been reported in recent years, its application in positron emission tomography tracer development is still an area of work in progress. This review summarizes all contributions to the area of radiolabeling using [(11) C]carbon monoxide published between 1995 and 2014 and discusses the scope and limitations of this method in clinical positron emission tomography tracer development.

  9. Development of carbon-11 labelled PET tracers-radiochemical and technological challenges in a historic perspective.

    PubMed

    Antoni, Gunnar

    2015-03-01

    The development of positron emission tomography (PET) from being an exclusive and expensive research tool at major research institutes to a clinically useful modality found at most major hospitals around the world is largely dependent on radiochemistry and synthesis technology achievements by a few pioneer researchers starting their PET careers 40 to 50 years ago. Especially, the introduction of [(11) C]methyl iodide resulted in a quantum jump in the history of PET tracer development enabling the smooth labelling of a multitude of useful tracers. A more recent and still challenging methodological improvement is transition metal mediated (11) C-carbonylations, having a large synthetic potential that has, however, not yet been realized in the clinical setting. This mini-review focuses on the history of carbon-11 radiochemistry and related technology developments and the role this played in PET tracer developments, especially emphasizing radiolabelling of endogenous compounds. A few examples will be presented of how the use of radiolabelled endogenous substances have provided fundamental information of in vivo biochemistry using the concept of position-specific labelling in different positions in the same molecule. PMID:25684179

  10. Relations between Light Level, Sucrose Concentration, and Translocation of Carbon 11 in Zea mays Leaves

    PubMed Central

    Troughton, John H.; Currie, B. G.; Chang, F. H.

    1977-01-01

    The mechanism of carbon transport in Zea mays leaves was investigated using carbon 11 which is a short lived (half-life 20.4 min) positronemitting isotope. The gamma radiation produced on annihilation allows in vivo or nondestructive measurement of the isotope and the short half-life allows many measurements of translocation to be made on the same leaf within the same day. Carbon 11 produced by the 10B (d,n)11C nuclear reaction was converted to 11CO2, fed to a leaf as a short pulse, and assimilated during photosynthesis. The progress of the radioactive pulse along the leaf in the phloem was monitored in several positions simultaneously with counters. The counters were NaI crystals with photomultipliers and the output was amplified, passed to single channel analyzers, and the counts accumulated for 20 seconds every 30 seconds. Corrections were made for the half-life and background radiation by computer, and the results were displayed on a high speed plotter. Information derived from the corrected data included the speed of translocation, the shape of the radioactive carbon pulse, and the influence of light and distance along the leaf on these parameters. The plants were kept under controlled environment conditions during all measurements. A speed was derived from the time displacement of the midpoint of the front of the pulse, measured at two positions along the leaf. This was an apparent mean speed of translocation because it averaged a variation in speed with distance, variation in speed between or within sieve tubes, and it averaged the mean speed of all of the particles in the pulse. A wide range of speeds of translocation from 0.25 to 11 cm min−1 was observed but most of the variability was due to the variation in light available to the leaf. For example, the speed of translocation was proportional to the light level on either the whole plant or individual leaf. Shading of the leaf established that the light effect was not localized in either the feeding area

  11. Carbon-11 labeled cathepsin K inhibitors: syntheses and preliminary in vivo evaluation.

    PubMed

    Rodnick, Melissa E; Shao, Xia; Kozloff, Kenneth M; Scott, Peter J H; Kilbourn, Michael R

    2014-01-01

    Cathepsin K is a cysteine peptidase primarily located in osteoclasts, cells involved in normal growth and remodeling of bone but that are also responsible for bone loss in osteolytic diseases such as osteoporosis. In vivo imaging of cathepsin K may provide a method to assess changes in osteoclast numbers in such disease states. To that end, two high-affinity and selective cathepsin K inhibitors were radiolabeled with carbon-11. In vivo microPET imaging studies demonstrated uptake and prolonged retention of radioactivity in actively growing or remodeling bone regions (e.g., distal ulnar, carpal, distal and proximal humeral, distal femur, proximal tibia, tail vertebrae). Uptake into bone could be blocked by pre- or co-injection of unlabeled ligand, supporting a specific and saturable binding mechanism for radiotracer localization. These proof-of-concept studies indicate that radiolabeled cathepsin K inhibitors may have potential as in vivo imaging radiotracers for assessing changes of osteoclast numbers in osteolytic diseases.

  12. SU-E-J-144: Low Activity Studies of Carbon 11 Activation Via GATE Monte Carlo

    SciTech Connect

    Elmekawy, A; Ewell, L; Butuceanu, C; Qu, L

    2015-06-15

    Purpose: To investigate the behavior of a Monte Carlo simulation code with low levels of activity (∼1,000Bq). Such activity levels are expected from phantoms and patients activated via a proton therapy beam. Methods: Three different ranges for a therapeutic proton radiation beam were examined in a Monte Carlo simulation code: 13.5, 17.0 and 21.0cm. For each range, the decay of an equivalent length{sup 11}C source and additional sources of length plus or minus one cm was studied in a benchmark PET simulation for activities of 1000, 2000 and 3000Bq. The ranges were chosen to coincide with a previous activation study, and the activities were chosen to coincide with the approximate level of isotope creation expected in a phantom or patient irradiated by a therapeutic proton beam. The GATE 7.0 simulation was completed on a cluster node, running Scientific Linux Carbon 6 (Red Hat©). The resulting Monte Carlo data were investigated with the ROOT (CERN) analysis tool. The half-life of{sup 11}C was extracted via a histogram fit to the number of simulated PET events vs. time. Results: The average slope of the deviation of the extracted carbon half life from the expected/nominal value vs. activity showed a generally positive value. This was unexpected, as the deviation should, in principal, decrease with increased activity and lower statistical uncertainty. Conclusion: For activity levels on the order of 1,000Bq, the behavior of a benchmark PET test was somewhat unexpected. It is important to be aware of the limitations of low activity PET images, and low activity Monte Carlo simulations. This work was funded in part by the Philips corporation.

  13. Studies of cryocooler based cryosorption pump with activated carbon panels operating at 11K

    NASA Astrophysics Data System (ADS)

    Kasthurirengan, S.; Behera, Upendra; Gangradey, Ranjana; Udgata, Swarup; Krishnamoorthy, V.

    2012-11-01

    Cryosorption pump is the only solution for pumping helium and hydrogen in fusion reactors. It is chosen because it offers highest pumping speed as well as the only suitable pump for the harsh environments in a tokamak. Towards the development of such cryosorption pumps, the optimal choice of the right activated carbon panels is essential. In order to characterize the performance of the panels with indigenously developed activated carbon, a cryocooler based cryosorption pump with scaled down sizes of panels is experimented. The results are compared with the commercial cryopanel used in a CTI cryosorption (model: Cryotorr 7) pump. The cryopanel is mounted on the cold head of the second stage GM cryocooler which cools the cryopanel down to 11K with first stage reaching about ~50K. With no heat load, cryopump gives the ultimate vacuum of 2.1E-7 mbar. The pumping speed of different gases such as nitrogen, argon, hydrogen, helium are tested both on indigenous and commercial cryopanel. These studies serve as a bench mark towards the development of better cryopanels to be cooled by liquid helium for use with tokamak.

  14. Studies and proposed changes to the RHIC p-Carbon polarimeters for the upcoming RUN-11

    SciTech Connect

    Makdisi, Y.; Alekseev, I.; Aschenauer, E.; Atoian, G.; Bazilevsky, A.; Gill, R.; Huang, H.; Morozov, B.; Svirida, D.; Yip, K.; Zelenski, A.

    2010-09-27

    The RHIC polarized proton complex utilizes polarimeters in each of the Blue and Yellow beams that measure the beam polarization through the p-Carbon elastic scattering process in the Coulomb Nuclear Interference kinematic region. This along with a Polarized Hydrogen Jet Target that utilizes the proton-proton elastic scattering process to first measure the analyzing power of the reaction and using the reverse process to measure the beam polarization. The latter is used to calibrate the p-Carbon polarimeters at the desired beam energy. In Run 9 RHIC ran with beams at center-of-mass energies of 200 and 500 GeV respectively. The higher beam intensities as well as the fact that the 250 GeV beam size is much smaller than that at 100 GeV resulted in significantly higher rates seen by the polarimeters and led to observed instability. In this paper, we will discuss the problems encountered and the tests that were carried out using the AGS as a proxy in an attempt to solve the problems and the path forward we took towards the upcoming polarized proton Run11.

  15. Carbon Counter-Electrode-Based Quantum-Dot-Sensitized Solar Cells with Certified Efficiency Exceeding 11.

    PubMed

    Du, Zhonglin; Pan, Zhenxiao; Fabregat-Santiago, Francisco; Zhao, Ke; Long, Donghui; Zhang, Hua; Zhao, Yixin; Zhong, Xinhua; Yu, Jong-Sung; Bisquert, Juan

    2016-08-18

    The mean power conversion efficiency (PCE) of quantum-dot-sensitized solar cells (QDSCs) is mainly limited by the low photovoltage and fill factor (FF), which are derived from the high redox potential of polysulfide electrolyte and the poor catalytic activity of the counter electrode (CE), respectively. Herein, we report that this problem is overcome by adopting Ti mesh supported mesoporous carbon (MC/Ti) CE. The confined area in Ti mesh substrate not only offers robust carbon film with submillimeter thickness to ensure high catalytic capacity, but also provides an efficient three-dimension electrical tunnel with better conductivity than state-of-art Cu2S/FTO CE. More importantly, the MC/Ti CE can down shift the redox potential of polysulfide electrolyte to promote high photovoltage. In all, MC/Ti CEs boost PCE of CdSe0.65Te0.35 QDSCs to a certified record of 11.16% (Jsc = 20.68 mA/cm(2), Voc = 0.798 V, FF = 0.677), an improvement of 24% related to previous record. This work thus paves a way for further improvement of performance of QDSCs. PMID:27455143

  16. Adrenal-derived 11-Oxygenated 19-Carbon Steroids are the Dominant Androgens in Classic 21-Hydroxylase Deficiency

    PubMed Central

    Turcu, Adina F.; Nanba, Aya T.; Chomic, Robert; Upadhyay, Sunil K.; Giordano, Thomas J.; Shields, James J.; Merke, Deborah P.; Rainey, William E.; Auchus, Richard J.

    2016-01-01

    Objective To comprehensively characterize androgens and androgen precursors in classic 21-hydroxylase deficiency (21OHD) and to gain insight to the mechanisms of their formation. Design Serum samples were obtained from 38 patients (19 men) with classic 21OHD, age 3-59, and 38 sex- and age-matched controls; 3 patients with 11β-hydroxylase deficiency; 4 patients with adrenal insufficiency; and 16 patients (8 men) undergoing adrenal vein sampling. Paraffin-embedded normal (n=5) and 21OHD adrenal tissue (n=3) was used for immunohistochemical studies. Methods We measured 11 steroids in all sera using liquid chromatography-tandem mass spectrometry. Immunofluroescence localized 3β-hydroxysteroid dehydrogenase type 2 (HSD3B2) and cytochrome b5 (CYB5A) within the normal and 21OHD adrenals. Results Four 11-oxygenated 19-carbon (11oxC19) steroids were significantly higher in male and female 21OHD patients than in controls: 11β-hydroxyandrostenedione, 11-ketoandrostenedione 11β-hydroxytestosterone, and 11-ketotestosterone (3-4-fold, p< 0.0001). For 21OHD patients, testosterone and 11-ketotestosterone were positively correlated in females, but inversely correlated in males. All 11oxC19 steroids were higher in adrenal vein than in inferior vena cava samples from men and women and rose with cosyntropin stimulation. Only trace amounts of 11oxC19 steroids were found in sera from patients with 11β-hydroxylase deficiency and adrenal insufficiency, confirming their adrenal origin. HSD3B2 and CYB5A immunoreactivities were sharply segregated in the normal adrenal glands, whereas areas of overlapping expression were identified in the 21OHD adrenals. Conclusions All four 11oxC19 steroids are elevated in both men and women with classic 21OHD. Our data suggest that 11oxC19 steroids are specific biomarkers of adrenal-derived androgen excess. PMID:26865584

  17. Simple synthesis of carbon-11 labeled styryl dyes as new potential PET RNA-specific, living cell imaging probes.

    PubMed

    Wang, Min; Gao, Mingzhang; Miller, Kathy D; Sledge, George W; Hutchins, Gary D; Zheng, Qi-Huang

    2009-05-01

    A new type of styryl dyes have been developed as RNA-specific, live cell imaging probes for fluorescent microscopy technology to study nuclear structure and function. This study was designed to develop carbon-11 labeled styryl dyes as new probes for biomedical imaging technique positron emission tomography (PET) imaging of RNA in living cells. Precursors (E)-2-(2-(1-(triisopropylsilyl)-1H-indol-3-yl)vinyl)quinoline (2), (E)-2-(2,4,6-trimethoxystyryl)quinoline (3) and (E)-4-(2-(6-methoxyquinolin-2-yl)vinyl)-N,N-diemthylaniline (4), and standards styryl dyes E36 (6), E144 (7) and F22 (9) were synthesized in multiple steps with moderate to high chemical yields. Precursor 2 was labeled by [(11)C]CH(3)OTf, trapped on a cation-exchange CM Sep-Pak cartridge following a quick deprotecting reaction by addition of (n-Bu)(4)NF in THF, and isolated by solid-phase extraction (SPE) purification to provide target tracer [(11)C]E36 ([(11)C]6) in 40-50% radiochemical yields, decay corrected to end of bombardment (EOB), based on [(11)C]CO(2). The target tracers [(11)C]E144 ([(11)C]7) and [(11)C]F22 ([(11)C]9) were prepared by N-[(11)C]methylation of the precursors 3 and 4, respectively, using [(11)C]CH(3)OTf and isolated by SPE method in 50-70% radiochemical yields at EOB. The specific activity of the target tracers [(11)C]6, [(11)C]7 and [(11)C]9 was in a range of 74-111GBq/mumol at the end of synthesis (EOS).

  18. Radiosynthesis of Carbon-11 Labeled Puromycin as a Potential PET Candidate for Imaging Protein Synthesis in Vivo.

    PubMed

    Milicevic Sephton, Selena; Aigbirhio, Franklin I

    2016-06-01

    In order to address the limitations associated with the present range of PET radiotracers used for imaging protein synthesis in vivo we have synthesized a candidate PET radiotracer based on Puromycin (3, PURO), a protein synthesis inhibitor. The desmethylPURO 9 precursor for radiolabeling with carbon-11 radioisotope was synthesized in two steps employing EDC/HOBt amide coupling in overall 76% yield. Optimal conditions for radiolabeling were then established via methylation/deprotection sequence. Under these conditions as determined by NMR analysis 9 showed partial stability (ca. 80%) under acidic conditions. Limited evidence of stereochemical stability of 3 was also found. The radiolabeling of intermediate [(11)C]12 was accomplished with up to 57% conversion from [(11)C]iodomethane. An automated method was then developed for high radioactivity radiosynthesis to produce [(11)C]3 ([(11)C]PURO) in 16 ± 6% (n = 3) decay corrected radiochemical yields. PMID:27326342

  19. Concentration and isotopic composition of carbon and sulfur in apollo 11 lunar samples.

    PubMed

    Kaplan, I R; Smith, J W

    1970-01-30

    The concentration of carbon and sulfur in six samples ranged between 20 to 200 and 650 to 2300 parts per million, respectively. Carbon was present in gaseous, volatilizable, and nonvolatile forms, and terrestrial contaminants were recognized. Sulfur appeared to exist only as acid-volatile sulfide. The bulk fines contain a high concentration of carbon and a low concentration of sulfur. They are always enriched in the heavier isotope carbon-13 or sulfur-34. The fine-grained basaltic rocks show the reverse relation; lowest carbon, highest sulfide concentrations, and no apparent enrichment in heavy isotopes. The breccias are of intermediate composition.

  20. Preclinical evaluation of carbon-11 and fluorine-18 sulfonamide derivatives for in vivo radiolabeling of erythrocytes

    PubMed Central

    2013-01-01

    Background To date, few PET tracers for in vivo labeling of red blood cells (RBCs) are available. In this study, we report the radiosynthesis and in vitro and in vivo evaluation of 11C and 18F sulfonamide derivatives targeting carbonic anhydrase II (CA II), a metallo-enzyme expressed in RBCs, as potential blood pool tracers. A proof-of-concept in vivo imaging study was performed to demonstrate the feasibility to assess cardiac function and volumes using electrocardiogram (ECG)-gated positron emission tomography (PET) acquisition in comparison with cine magnetic resonance imaging (cMRI) in rats and a pig model of myocardial infarction. Methods The inhibition constants (Ki) of CA II were determined in vitro for the different compounds by assaying CA-catalyzed CO2 hydration activity. Binding to human RBCs was estimated after in vitro incubation of the compounds with whole blood. Biodistribution studies were performed to evaluate tracer kinetics in NMRI mice. ECG-gated PET acquisition was performed in Wistar rats at rest and during pharmacological stress by infusing dobutamine at 10 μg/kg/min and in a pig model of myocardial infarction. Left ventricular ejection fraction (LVEF) and volumes were compared with values from cMRI. Results The Ki of the investigated compounds for human CA II was found to be in the range of 8 to 422 nM. The fraction of radioactivity associated with RBCs was found to be ≥90% at 10- and 60-min incubation of tracers with heparinized human blood at room temperature for all tracers studied. Biodistribution studies in mice indicated that 30% to 67% of the injected dose was retained in the blood pool at 60 min post injection. A rapid and sustained tracer uptake in the heart region with an average standardized uptake value of 2.5 was observed from micro-PET images. The LVEF values obtained after pharmacological stress in rats closely matched between the cMRI and micro-PET values, whereas at rest, a larger variation between LVEF values obtained by

  1. 11 things a geologist thinks an engineer should know about carbonate beaches

    USGS Publications Warehouse

    Halley, R.B.; ,

    2000-01-01

    A review is given on the geological aspects of carbonate beaches that a geologist thinks may be useful for an engineer. Though, Geologists not involved in engineering problems may find it difficult to know what an engineer should understand about carbonate beaches. Nevertheless, there are at least eleven topics that are potentially very useful for engineers to keep in mind. This paper emits the discussions of certain kinds of carbonate shorelines that are beyond the scope of engineering issues, and focuses on sand-sized coastal carbonate deposits.

  2. Non-Detection of HC11N toward TMC-1: Constraining the Chemistry of Large Carbon-Chain Molecules

    NASA Astrophysics Data System (ADS)

    Loomis, Ryan A.; Shingledecker, Christopher N.; Langston, Glen; McGuire, Brett A.; Dollhopf, Niklaus M.; Burkhardt, Andrew M.; Corby, Joanna; Booth, Shawn T.; Carroll, P. Brandon; Turner, Barry; Remijan, Anthony J.

    2016-09-01

    Bell et al. (1997) reported the first detection of the cyanopolyyne HC11N toward the cold dark cloud TMC-1; no subsequent detections have been reported toward any source. Additional observations of cyanopolyynes and other carbon-chain molecules toward TMC-1 have shown a log-linear trend between molecule size and column density, and in an effort to further explore the underlying chemical processes driving this trend, we have analyzed GBT observations of HC9N and HC11N toward TMC-1. Although we find an HC9N column density consistent with previous values, HC11N is not detected and we derive an upper limit column density significantly below that reported in Bell et al. (1997). Using a state-of-the-art chemical model, we have investigated possible explanations of non-linearity in the column density trend. Despite updating the chemical model to better account for ion-dipole interactions, we are not able to explain the non-detection of HC11N, and we interpret this as evidence of previously unknown carbon-chain chemistry. We propose that cyclization reactions may be responsible for the depleted HC11N abundance, and that products of these cyclization reactions should be investigated as candidate interstellar molecules.

  3. 11 things a geologist thinks an engineer should know about carbonate beaches

    USGS Publications Warehouse

    Halley, Robert B.; Magoon, Orville T.; Robbins, Lisa L.; Ewing, Lesley

    2002-01-01

    This is a review of the geological aspects of carbonate beaches that a geologist thinks may be useful for an engineer. Classical geologic problems of carbonate beaches, for example how ancient examples are recognized in rock sequences, are of little interest to engineers. Geologists not involved in engineering problems may find it difficult to know what an engineer should understand about carbonate beaches. Nevertheless, there are at least eleven topics that are potentially very useful for engineers to keep in mind. These eleven are chosen with as much thought going into what has been omitted as has been given to the eleven included topics. Some qualifications are in order: First, this paper does not discuss certain kinds of carbonate shorelines that are beyond the scope of engineering issues. For example, this review does not discuss very high-energy carbonate boulder beaches. These beaches are comprised of pieces of carbonate material ganging in size from ten centimeters to meters. Typically, these are high-energy storm deposits formed from pieces of either eroded carbonate rock or other large carbonate pieces such as pieces of large corals. This paper focuses on sand-sized (0.0625–2.0 mm) coastal carbonate deposits. Second, offshore beaches will not be discussed. There are many carbonate beaches that form on banks or shoals exposed at low tide, but our discussion is confined to what most people think of when they go to some tropical island and/or resort and walk out to lay on the beach. Third, this paper does not consider mixed carbonate/quartz sand beaches. While mixed beaches are common, only the end member of purely carbonate sand beaches is considered. Fourth, there will be no order of preference of the eleven topics. And lastly, these eleven topics are not consensus items. These are simply one geologist s thoughts about the aspects of carbonate beaches that would be useful for engineering colleagues to keep in mind. Where possible, general reference is

  4. Rotational Spectrum and Structure of the 1,1-Difluoroethylene···Carbon Dioxide Complex.

    PubMed

    Anderton, Ashley M; Peebles, Rebecca A; Peebles, Sean A

    2016-01-21

    Rotational spectra for five isotopologues of the 1:1 weak complex between 1,1-difluoroethylene (H2C═CF2) and carbon dioxide (CO2) have been measured using 480 MHz bandwidth chirped-pulse and resonant cavity Fourier-transform microwave spectroscopy between 5.5 and 18.5 GHz. The observed structure of the complex is planar, with the CO2 aligned roughly parallel to the C═C bond, and experimental structural parameters derived from rotational constants are consistent with the most stable geometry predicted by basis set superposition error and zero point energy corrected ab initio geometry optimizations at the MP2/6-311++G(2d,2p) level. Comparisons with the recently characterized vinyl fluoride···carbon dioxide complex reveal slightly longer intermolecular distances in the present complex, but very similar binding energies.

  5. Biodistribution of a positron-emitting suicide inactivator of monoamine oxidase, carbon-11 pargyline, in mice and a rabbit

    SciTech Connect

    Ishiwata, K.; Ido, T.; Yanai, K.; Kawashima, K.; Miura, Y.; Monma, M.; Watanuki, S.; Takahashi, T.; Iwata, R.

    1985-06-01

    Carbon-11 (/sup 11/C) pargyline, which is a suicide inactivator of Type B monoamine oxidase (MAO), was synthesized by the reaction of N-demethylpargyline with /sup 11/CH/sub 3/l. Biodistribution was investigated in mice, and positron tomographic images of the heart and lung in a rabbit were obtained. The distribution of /sup 11/C after administration of (/sup 11/C)pargyline was measured in several organs and blood at various time intervals. After 30 min its concentrations in the organs were constant. Subcellular distribution studies in the brain, lung, liver, and kidney showed that 59-70% of the /sup 11/C became acid-insoluble and 9-33% was present in the crude mitochondrial fraction at 60 min after injection. The uptakes of the /sup 11/C in each organ except for the kidney and spleen seemed to correlate with the in vitro enzymatic activity of Type B MAO. At high loading dose a nonspecific uptake was observed.

  6. Stable isotopic compositions of elemental carbon in PM1.1 in north suburb of Nanjing Region, China

    NASA Astrophysics Data System (ADS)

    Guo, Zhaobing; Jiang, Wenjuan; Chen, Shanli; Sun, Deling; Shi, Lei; Zeng, Gang; Rui, Maoling

    2016-02-01

    Stable isotopic compositions (δ13C) of elemental carbon (EC) in PM1.1 in north suburb of Nanjing region were determined in order to quantitatively evaluate the carbon sources of atmospheric fine particles during different seasons. Besides, δ13C values from potential sources such as coal combustion, vehicle exhaust, biomass burning, and dust were synchronously measured. The results showed that the average δ13C values of EC in PM1.1 in winter and summer were - 23.89 ± 1.6‰ and - 24.76 ± 0.9‰, respectively. Comparing with δ13C values from potential sources, we concluded that the main sources of EC in PM1.1 were from the emission of coal combustion and vehicle exhaust. The higher δ13C values in winter than those in summer were chiefly attributed to the more coal consumption. Combining with the concentrations of SO42 - and K+ in PM1.1, the high δ13C values of EC on 24 December and 27 December 2013 were ascribed to extra input of corn straw burning in addition to coal combustion and vehicle exhaust.

  7. Carbon Isotope Fractionation of 11 Acetogenic Strains Grown on H2 and CO2

    PubMed Central

    Dreisbach, Lisa K.; Conrad, Ralf

    2013-01-01

    Acetogenic bacteria are able to grow autotrophically on hydrogen and carbon dioxide by using the acetyl coenzyme A (acetyl-CoA) pathway. Acetate is the end product of this reaction. In contrast to the fermentative route of acetate production, which shows almost no fractionation of carbon isotopes, the acetyl-CoA pathway has been reported to exhibit a preference for light carbon. In Acetobacterium woodii the isotope fractionation factor (ε) for 13C and 12C has previously been reported to be ε = −58.6‰. To investigate whether such a strong fractionation is a general feature of acetogenic bacteria, we measured the stable carbon isotope fractionation factor of 10 acetogenic strains grown on H2 and CO2. The average fractionation factor was εTIC = −57.2‰ for utilization of total inorganic carbon and εacetate = −54.6‰ for the production of acetate. The strongest fractionation was found for Sporomusa sphaeroides (εTIC = −68.3‰), the lowest fractionation for Morella thermoacetica (εTIC = −38.2‰). To investigate the reproducibility of our measurements, we determined the fractionation factor of 21 biological replicates of Thermoanaerobacter kivui. In general, our study confirmed the strong fractionation of stable carbon during chemolithotrophic acetate formation in acetogenic bacteria. However, the specific characteristics of the bacterial strain, as well as the cultural conditions, may have a moderate influence on the overall fractionation. PMID:23275504

  8. Total cyanide mass measurement with micro-ion selective electrode for determination of specific activity of carbon-11 cyanide.

    PubMed

    Shea, Colleen; Alexoff, David L; Kim, Dohyun; Hoque, Ruma; Schueller, Michael J; Fowler, Joanna S; Qu, Wenchao

    2015-08-01

    In this research, we aim to directly measure the specific activity (SA) of the carbon-11 cyanide ([(11)C]CN¯) produced by our in-house built automated [(11)C]HCN production system and to identify the major sources of (12)C-cyanide ((12)CN¯). The [(11)C]CN¯ is produced from [(11)C]CO2, which is generated by the (14)N(p,α)(11)C nuclear reaction using a cyclotron. Direct measurement of cyanide concentrations was accomplished using a relatively inexpensive, and easy to use ion selective electrode (ISE) which offered an appropriate range of sensitivity for detecting mass. Multiple components of the [(11)C]HCN production system were isolated in order to determine their relative contributions to (12)CN¯ mass. It was determined that the system gases were responsible for approximately 30% of the mass, and that the molecular sieve/nickel furnace unit contributed approximately 70% of the mass. Beam on target (33µA for 1 and 10min) did not contribute significantly to the mass. Additionally, we compared the SA of our [(11)C]HCN precursor determined using the ISE to the SA of our current [(11)C]CN¯ derived radiotracers determined by HPLC to assure there was no significant difference between the two methods. These results are the first reported use of an ion selective electrode to determine the SA of no-carrier-added cyanide ion, and clearly show that it is a valuable, inexpensive and readily available tool suitable for this purpose.

  9. Total cyanide mass measurement with micro-ion selective electrode for determination of specific activity of carbon-11 cyanide

    DOE PAGES

    Shea, Colleen; Alexoff, David L.; Kim, Dohyun; Hoque, Ruma; Schueller, Michael J.; Fowler, Joanna S.; Qu, Wenchao

    2015-04-25

    In this study, we aim to directly measure the specific activity (SA) of the carbon-11 cyanide ([11C]CN¯) produced by our in-house built automated [11C]HCN production system and to identify the major sources of 12C-cyanide (12CN¯). The [11C]CN¯ is produced from [11C]CO2, which is generated by the 14N(p,α)11C nuclear reaction using a cyclotron. Direct measurement of cyanide concentrations was accomplished using a relatively inexpensive, and easy to use ion selective electrode (ISE) which offered an appropriate range of sensitivity for detecting mass. Multiple components of the [11C]HCN production system were isolated in order to determine their relative contributions to 12CN¯ mass.more » It was determined that the system gases were responsible for approximately 30% of the mass, and that the molecular sieve/nickel furnace unit contributed approximately 70% of the mass. Beam on target (33 µA for 1 and 10 min) did not contribute significantly to the mass. Additionally, we compared the SA of our [11C]HCN precursor determined using the ISE to the SA of our current [11C]CN¯ derived radiotracers determined by HPLC to assure there was no significant difference between the two methods. These results are the first reported use of an ion selective electrode to determine the SA of no-carrier-added cyanide ion, and clearly show that it is a valuable, inexpensive and readily available tool suitable for this purpose.« less

  10. Total cyanide mass measurement with micro-ion selective electrode for determination of specific activity of carbon-11 cyanide

    SciTech Connect

    Shea, Colleen; Alexoff, David L.; Kim, Dohyun; Hoque, Ruma; Schueller, Michael J.; Fowler, Joanna S.; Qu, Wenchao

    2015-04-25

    In this study, we aim to directly measure the specific activity (SA) of the carbon-11 cyanide ([11C]CN¯) produced by our in-house built automated [11C]HCN production system and to identify the major sources of 12C-cyanide (12CN¯). The [11C]CN¯ is produced from [11C]CO2, which is generated by the 14N(p,α)11C nuclear reaction using a cyclotron. Direct measurement of cyanide concentrations was accomplished using a relatively inexpensive, and easy to use ion selective electrode (ISE) which offered an appropriate range of sensitivity for detecting mass. Multiple components of the [11C]HCN production system were isolated in order to determine their relative contributions to 12CN¯ mass. It was determined that the system gases were responsible for approximately 30% of the mass, and that the molecular sieve/nickel furnace unit contributed approximately 70% of the mass. Beam on target (33 µA for 1 and 10 min) did not contribute significantly to the mass. Additionally, we compared the SA of our [11C]HCN precursor determined using the ISE to the SA of our current [11C]CN¯ derived radiotracers determined by HPLC to assure there was no significant difference between the two methods. These results are the first reported use of an ion selective electrode to determine the SA of no-carrier-added cyanide ion, and clearly show that it is a valuable, inexpensive and readily available tool suitable for this purpose.

  11. Carbon-11 and radioiodinated derivatives of lysergic acid diethylamide: Ligands for the study of serotonin S2 receptors in vivo

    SciTech Connect

    Lever, J.R.; Hartig, P.R.; Wong, D.F.; Scheffel, U.; Dannals, R.F.; Wilson, A.A.; Ravert, H.T.; Hoffman, B.J.; Frost, J.J.; Burns, H.D.

    1985-05-01

    2-(/sup 125/1)-LSD binds selectively and with high affinity to serotonin S2 receptors in vitro. In the present study, the authors prepared 2-(/sup 123/1)-LSD as well as a carbon-11 labeled analog. They also characterized the in vivo binding of these tracers to receptor sites in mouse brain to assess their potential for tomographic imaging of S2 receptors in man. The temporal distribution of 2-(/sup 125/1)-LSD paralleled the density of S2 receptors. Regional selectivity was maximal after 15 minutes when tissue to cerebellum ratios were: frontal cortex (2.6), olfactory tubercles (2.4), striatum (2.3), and cortex (2.0). Preinjection of ketanserin, a potent S2 antagonist, inhibited binding. 2-(/sup 123/1)-LSD, prepared in 20% yield from LSD and electrophilic I-123, gave similar results in vivo and may be useful for SPECT studies. The authors then synthesized N1-((/sup 11/C)-Me)-2-Br-LSD (/sup 11/C-MBL) from (/sup 11/C)-methyl iodide and 2-Br-LSD for PET imaging trials. /sup 11/C-MBL was isolated by HPLC in high chemical and radiochemical purity within 30 minutes from E.O.B. The average radiochemical yield was 20% and the specific activity was determined by U.V. spectroscopy to be up to 1300Ci/mMol (E.O.S.). 11C-MBL showed greater regional selectivity in vivo in mouse brain than 2-(/sup 125/1)-LSD. After 30 minutes, peak tissue to cerebellum ratios were: frontal cortex (5.4), olfactory tubercles (4.2), striatum (3.0), and cortex (2.8). Preinjection of ketanserin markedly inhibited /sup 11/C-MBL binding. /sup 11/C-MBL is a promising candidate for PET studies of S2 receptors.

  12. Carbon-11-cocaine binding compared at subpharmacological and pharmacological doses: A PET study

    SciTech Connect

    Volkow, N.D.; Fowler, J.S.; Logan, J. |

    1995-07-01

    The authors have characterized cocaine binding in the brain to a high-affinity site on the dopamine transporter using PET and tracer doses of [{sup 11}C]cocaine in the baboon in vivo. The binding pattern, however, of cocaine at tracer (subpharmacological) doses may differ from that observed when the drug is taken in behaviorally active doses, particularly since in vitro studies have shown that cocaine also binds to low affinity binding sites. PET was used to compare and characterize [{sup 11}C]cocaine binding in the baboon brain at low subpharmacological (18 {mu}g average dose) and at pharmacological (8000 {mu}g) doses. Serial studies on the same day in the same baboon were used to assess the reproducibility of repeated measures and to assess the effects of drugs which inhibit the dopamine, norepinephrine and serotonin transporters. Time-activity curves from brain and the arterial plasma input function were used to calculate the steady-state distribution volume (DV). At subpharmacological doses, [{sup 11}C]cocaine had a more homogeneous distribution. Bmax/Kd for sub-pharmacological [{sup 11}C]cocaine corresponded to 0.5-0.6 and for pharmacological [{sup 11}C]cocaine it corresponded to 0.1-0.2. Two-point Scatchard analysis gave Bmax = 2300 pmole/g and Kd = 3600 nM. Bmax/Kd for sub-pharmacological doses of [{sup 11}C]cocaine was decreased by cocaine and drugs that inhibit the dopamine transporter, to 0.1-0.2, but not by drugs that inhibit the serotonin or the norepinephrine transporter. None of these drugs changed Bmax/Kd for a pharmacological dose of [{sup 11}C]cocaine. At subpharmacological doses, [{sup 11}C]cocaine binds predominantly to a high-affinity site on the dopamine transporter. 36 refs., 4 figs., 5 tabs.

  13. Noninvasive estimation of regional myocardial oxygen consumption by positron emission tomography with carbon-11 acetate in patients with myocardial infarction

    SciTech Connect

    Walsh, M.N.; Geltman, E.M.; Brown, M.A.; Henes, C.G.; Weinheimer, C.J.; Sobel, B.E.; Bergmann, S.R. )

    1989-11-01

    We previously demonstrated in experimental studies that myocardial oxygen consumption (MVO2) can be estimated noninvasively with positron emission tomography (PET) from analysis of the myocardial turnover rate constant (k) after administration of carbon-11 (11C) acetate. To determine regional k in healthy human subjects and to estimate alterations in MVO2 accompanying myocardial ischemia, we administered (11C)acetate to five healthy human volunteers and to six patients with myocardial infarction. Extraction of (11C)acetate by the myocardium was avid and clearance from the blood-pool rapid yielding myocardial images of excellent quality. Regional k was homogeneous in myocardium of healthy volunteers (coefficient variation = 11%). In patients, k in regions remote from the area of infarction was not different from values in myocardium of healthy human volunteers (0.061 +/- 0.025 compared with 0.057 +/- 0.008 min-1). In contrast, MVO2 in the center of the infarct region was only 6% of that in remote regions (p less than 0.01). In four patients studied within 48 hr of infarction and again more than seven days after the acute event, regional k and MVO2 did not change. The approach developed should facilitate evaluation of the efficacy of interventions designed to enhance recovery of jeopardized myocardium and permit estimation of regional MVO2 and metabolic reserve underlying cardiac disease of diverse etiologies.

  14. In vivo measurement of carbon-11 thymidine uptake in non-Hodgkin's lymphoma using positron emission tomography

    SciTech Connect

    Martiat, P.; Ferrant, A.; Labar, D.; Cogneau, M.; Bol, A.; Michel, C.; Michaux, J.L.; Sokal, G.

    1988-10-01

    Carbon-11 thymidine (TdR) uptake using positron emission tomography (PET) has been measured in ten patients with non-Hodgkin's lymphoma (NHL). The rate of TdR uptake (mean +/- s.d.) was of 0.009 +/- 0.006 mumol.100 cc-1.min-1 in low-grade NHL. This rate was 0.063 +/- 0.049 mumol.100 cc-1.min-1 in intermediate-grade NHL and 0.159 mumol.100 cc-1.min-1 in a patient with high-grade NHL. Lymphoma radioactivity reached a plateau at 0.42 +/- 0.22%. 100 cc-1 of the injected dose from 10 min after injection. The highest /sup 11/C uptakes were observed in the kidneys and in the liver (3.30 +/- 1.30 and 2.10 +/- 0.05%. 100 cc-1 of the injected dose, respectively). The lymphoma-to-muscle ratio was of 11.8 +/- 1.7, whereas the lymphoma-to-intestine ratio was of 1.5 +/- 0.7. Accordingly, the measurement of (/sup 11/C)TdR uptake in the abdomen may need other imaging methods for adequate interpretation. The results suggest that (/sup 11/C)TdR uptake using PET might be a method for noninvasively measuring cell proliferation in vivo.

  15. Carbon-11-methionine and PET in evaluation of treatment response of breast cancer.

    PubMed Central

    Huovinen, R.; Leskinen-Kallio, S.; Någren, K.; Lehikoinen, P.; Ruotsalainen, U.; Teräs, M.

    1993-01-01

    Uptake of L-methyl-11C-methionine (11C-methionine) in breast cancer metastases was studied with positron emission tomography (PET). Eight patients with soft tissue metastases were studied twice: before the onset of chemotherapy (4), hormonal therapy (3) or radiotherapy (1) and 3-14 weeks later. The radioactivity concentration of the low molecular weight fraction of venous plasma samples separated by fast gel filtration was used as input function. The input corrected uptake rate of 11C-methionine (Ki) in breast cancer metastases before the treatment ranged between 0.035 and 0.186 1 min-1 and the standardised uptake value (SUV) between 2.0 and 11.4. The uptake of 11C-methionine into the metastases decreased when clinical objective stability or regression of the metastases was later obtained and increased in cases where progressive disease was seen during treatment. We conclude that metabolic changes in the amino acid metabolism detected by PET precede the clinical response, and may be of clinical value in predicting the treatment response. Images Figure 1 PMID:8471437

  16. Evaluation of DNA synthesis with carbon-11-labeled 4′-thiothymidine

    PubMed Central

    Toyohara, Jun

    2016-01-01

    In the cancer research field, the preferred method for evaluating the proliferative activity of cancer cells in vivo is to measure DNA synthesis rates. The cellular proliferation rate is one of the most important cancer characteristics, and represents the gold standard of pathological diagnosis. Positron emission tomography (PET) has been used to evaluate in vivo DNA synthetic activity through visualization of enhanced nucleoside metabolism. However, methods for the quantitative measurement of DNA synthesis rates have not been fully clarified. Several groups have been engaged in research on 4′-[methyl-11C]-thiothymidine (11C-4DST) in an effort to develop a PET tracer that allows quantitative measurement of in vivo DNA synthesis rates. This mini-review summarizes the results of recent studies of the in vivo measurement of cancer DNA synthesis rates using 11C-4DST. PMID:27721942

  17. Carbon-11 labeling of CP-126,998*: A radiotracer for in vivo studies of acetylcholinesterase

    SciTech Connect

    Musachio, J.L.; Flesher, J.E.; Scheffel, U.

    1996-05-01

    The study of acetylcholinesterase (AChE) via PET is of interest as reduced activity of this enzyme has been observed in Alzheimer`s disease. Our efforts to develop a radiotracer for mapping of AChE have focused on the N-benzylpiperidine benzisoxazole, CP-126,998, a highly potent (IC{sub 50}=0.48 nm) and selective inhibitor of AChE. High specific activity [C-11] CP-126,998 was synthesized (14 - 24% radiochemical yield, non-decay corrected) by treatment of the desmethyl precursor, CP-118,954, with [C-11] methyl iodide and tetrabutylammonium hydroxide in DMF. In vivo studies with [C-11] CP-126,998 in mice show that this radiotracer displays highest uptake in striatum (6.2 %ID/g), a brain region known to be rich in AChE. The (striatum-cerebellum)/cerebellar radioactivity ratio reached a maximum of 4.3 at 30 min postinjection, and this ratio decreased to 2.4 at 120 min. .Radiotracer binding was saturable in vivo by pretreatment with CP-118,954. Pretreatment of mice with diisopropylfluorophosphate (4 mg/kg i.p.), a known AChE inhibitor, significantly inhibited binding in striatum in a dose-dependent manner. Initial results suggest that [C-11] CP-126,998 may prove useful as a marker for the study of AChE in humans via PET.

  18. Radiation absorbed dose estimates for [1-carbon-11]-glucose in adults: The effects of hyperinsulinemia

    SciTech Connect

    Powers, W.J. |

    1996-10-01

    As preparation for studies of blood-brain glucose transport in diabetes mellitus, radiation absorbed dose estimates from intravenous administration of [1-{sup 11}C]-glucose for 24 internal organs, lens, blood and total body were calculated for three physiologic conditions: euinsulinemic euglycemia, hyperinsulinemic euglycemia and hyperinsulinemic hyperglycemia. Cumulated activities in blood, insulin-independent and insulin-dependent compartments were calculated from blood time-activity curves in normal human volunteers and macaques. Apportionment of cumulated activity to individual organs in insulin-dependent and insulin-independent compartments was based on previously published data. Absorbed doses were calculated with the computer program MIRDOSE 3 for the 70-kg adult phantom. S for blood was calculated separately. The heart wall, lungs and spleen were the organs receiving the highest dose. The effect of hyperinsulinemia was demonstrated by the increase in adsorbed dose to the muscle, heart and blood with a decrease to other internal organs. This effect was more pronounced during hyperinsulinemic hyperglycemia. Hyperinsulinemia produced a decrease in effective dose due to the decrease in cumulated activity in organs with specified weighting factors greater than 0.05. The effective dose per study for [1-{sup 11}C]-glucose is comparable to that reported for 2-deoxy-[2-{sup 18}F]-glucose. 43 refs., 1 fig., 4 tabs.

  19. BML-11, a lipoxin receptor agonist, protected carbon tetrachloride-induced hepatic fibrosis in rats.

    PubMed

    Zhou, Xiao-Yan; Yu, Zhong-Jian; Yan, Dan; Wang, Hong-Mei; Huang, Yong-Hong; Sha, Juan; Xu, Fang-Yun; Cai, Zhen-Yu; Min, Wei-Ping

    2013-10-01

    Inflammation plays an important role in the occurrence and development of fibrosis. Lipoxins (LXs) and BML-111 (lipoxin A4 agonist) have been approved for potent anti-inflammatory properties. Previously, we and others had showed LXs and BML-111 could protect acute hepatic injury, inhibit the growth and invasion of hepatic tumor. However, there are few reports dealing with their effects on hepatic fibrosis. To explore whether LXs and the analog could interrupt the process of hepatic fibrosis, the effects of BML-111 on tetrachloride-induced hepatic fibrosis were observed and the possible mechanism were discussed. Sprague-Dawley rats were induced liver fibrosis by carbon tetrachloride (CCl4) for 10 weeks with or without BML-111, and the histopathology and collagen content were employed to quantify hepatic necro-inflammation and fibrosis. Moreover, the expression levels of α-smooth muscle actin (α-SMA), transforming growth factor-β1 (TGF-β1), and platelet-derived growth factor (PDGF) were examined via Western blot or ELISA. Rats treated with BML-111 improved hepatic necro-inflammation and inhibited hepatic fibrosis in association with reduction of α-SMA expression and decreased collagen deposition. Furthermore, BML-111 could downregulate the expressions of TGF-β1 and PDGF significantly. BML-111 played a critical protective role in CCl4-induced hepatic fibrosis through inhibiting the levels of TGF-β1 and PDGF in rats.

  20. Isotope-Labeling Studies Support the Electrophilic Compound I Iron Active Species, FeO(3+), for the Carbon-Carbon Bond Cleavage Reaction of the Cholesterol Side-Chain Cleavage Enzyme, Cytochrome P450 11A1.

    PubMed

    Yoshimoto, Francis K; Jung, I-Ji; Goyal, Sandeep; Gonzalez, Eric; Guengerich, F Peter

    2016-09-21

    The enzyme cytochrome P450 11A1 cleaves the C20-C22 carbon-carbon bond of cholesterol to form pregnenolone, the first 21-carbon precursor of all steroid hormones. Various reaction mechanisms are possible for the carbon-carbon bond cleavage step of P450 11A1, and most current proposals involve the oxoferryl active species, Compound I (FeO(3+)). Compound I can either (i) abstract an O-H hydrogen atom or (ii) be attacked by a nucleophilic hydroxy group of its substrate, 20R,22R-dihydroxycholesterol. The mechanism of this carbon-carbon bond cleavage step was tested using (18)O-labeled molecular oxygen and purified P450 11A1. P450 11A1 was incubated with 20R,22R-dihydroxycholesterol in the presence of molecular oxygen ((18)O2), and coupled assays were used to trap the labile (18)O atoms in the enzymatic products (i.e., isocaproaldehyde and pregnenolone). The resulting products were derivatized and the (18)O content was analyzed by high-resolution mass spectrometry. P450 11A1 showed no incorporation of an (18)O atom into either of its carbon-carbon bond cleavage products, pregnenolone and isocaproaldehyde . The positive control experiments established retention of the carbonyl oxygens in the enzymatic products during the trapping and derivatization processes. These results reveal a mechanism involving an electrophilic Compound I species that reacts with nucleophilic hydroxy groups in the 20R,22R-dihydroxycholesterol intermediate of the P450 11A1 reaction to produce the key steroid pregnenolone.

  1. Taking out one billion tones of carbon: the magic of China's 11thFive-Year Plan

    SciTech Connect

    Lin, Jiang; Zhou, Nan; Levine, Mark D.; Fridley, David

    2007-05-01

    China's 11th Five-Year Plan (FYP) sets an ambitious targetfor energy-efficiency improvement: energy intensity of the country sgross domestic product (GDP) should be reduced by 20 percent from 2005 to2010 (NDRC, 2006). This is the first time that a quantitative and bindingtarget has been set for energy efficiency, and signals a major shift inChina's strategic thinking about its long-term economic and energydevelopment. The 20 percent energy intensity target also translates intoan annual reduction of over one billion tons of CO2 by 2010, making theChinese effort one of most significant carbon mitigation effort in theworld today. While it is still too early to tell whether China willachieve this target, this paper attempts to understand the trend inenergy intensity in China and to explore a variety of options towardmeeting the 20 percent target using a detailed endues energymodel.

  2. Mathematical modeling of enzyme production using Trichoderma harzianum P49P11 and sugarcane bagasse as carbon source.

    PubMed

    Gelain, Lucas; da Cruz Pradella, José Geraldo; da Costa, Aline Carvalho

    2015-12-01

    A mathematical model to describe the kinetics of enzyme production by the filamentous fungus Trichoderma harzianum P49P11 was developed using a low cost substrate as main carbon source (pretreated sugarcane bagasse). The model describes the cell growth, variation of substrate concentration and production of three kinds of enzymes (cellulases, beta-glucosidase and xylanase) in different sugarcane bagasse concentrations (5; 10; 20; 30; 40 gL(-1)). The 10 gL(-1) concentration was used to validate the model and the other to parameter estimation. The model for enzyme production has terms implicitly representing induction and repression. Substrate variation was represented by a simple degradation rate. The models seem to represent well the kinetics with a good fit for the majority of the assays. Validation results indicate that the models are adequate to represent the kinetics for a biotechnological process. PMID:26378961

  3. Unsymmetrical 1,1-diborated multisubstituted sp(3)-carbons formed via a metal-free concerted-asynchronous mechanism.

    PubMed

    Cuenca, Ana B; Cid, Jessica; García-López, Diego; Carbó, Jorge J; Fernández, Elena

    2015-10-01

    We have experimentally proved the unsymmetrical 1,1-diboration of diazo compounds, formed in situ from aldehydes and cyclic and non-cyclic ketones, in the absence of any transition metal complex. The heterolytic cleavage of the mixed diboron reagent, Bpin-Bdan, and the formation of two geminal C-Bpin and C-Bdan bonds has been rationalised based on DFT calculations to occur via a concerted-asynchronous mechanism. Diastereoselection is attained on substituted cyclohexanones and DFT studies provide understanding on the origin of the selectivity. The alkoxide-assisted selective deborylation of Bpin from multisubstituted sp(3)-carbon and generation of a Bdan stabilized carbanion, easily conducts a selective protodeboronation sequence.

  4. No-carrier-added carbon-11-labeled sn-1,2- and sn-1,3-diacylglycerols by (11C)propyl ketene method

    SciTech Connect

    Imahori, Y.; Fujii, R.; Ueda, S.; Ido, T.; Nishino, H.; Moriyama, Y.; Yamamoto, Y.L.; Nakahashi, H. )

    1991-08-01

    This article describes the preparation of sn-1,2-(11C)diacylglycerols and sn-1,3-(11C)diacylglycerols by a no-carrier-added reaction based on a labeling method using (1-11C)propyl ketene, which is one of the most potent acylating agents. (1-11C)Propyl ketene was produced by pyrolytic decomposition of (1-11C)butyric acid and was trapped in pyridine containing L-alpha-palmitoyl-lysophosphatidylcholine, producing L-alpha-palmitoyl-2-(1-11C)butyryl-sn-glycero-3-phosphorylcholine. The authors adopted an enzymatic reaction to remove the phosphorylcholine, in which L-alpha-palmitoyl-2-(1-11C)butyryl-sn-glycero-3-phosphorylcholine was incubated with phospholipase C, hydrolyzing to produce 1-palmitoyl-sn-2-(1-11C)butyrylglycerol. Total synthesis time was about 50 minutes and the specific activity was estimated at 93 GBq/mumol (2.5 Ci/mumol) at end of synthesis. Radiochemical yield was 3.8% based on the trapped 11CO2. sn-1,3-(11C)Diacylglycerol was also synthesized by (1-11C)propyl ketene reaction with 1-palmitoyl-sn-glycerol in a single procedure. The regional brain tissue radioactivities obtained in sn-1,2-(11C)diacylglycerol were higher than those of sn-1,3-(11C)diacylglycerol, and the regional values varied widely. In autoradiography of brain slices from conscious rats, sn-1,2-(11C)diacylglycerol incorporation sites were discretely localized, especially in the amygdala, cerebral cortex, and hippocampus, suggesting that intensive neuronal processing occurred in these areas on the basis of phosphatidylinositol turnover.

  5. In-place electrically heated regeneration of vapor-phase activated carbon. Final report, 11 July 1989-11 April 1990

    SciTech Connect

    Levy, R.; Hicks, R.E.; Gold, H.

    1990-09-01

    The Air Force is using the air stripping process to remove a variety of volatile organic contaminants from groundwater. Vapor-phase granular activated carbon (GAC) has proven successful in treating the contaminated air stream emanating from air stripping columns. but conventional regeneration methods are expensive, require transfer of the carbon. and degrade the carbon. The objective of this experimental program was to determine the feasibility of using electrically-heated processes for the in-place regeneration of vapor-phase GAC. Two processes were considered, namely microwave heating and electric resistance heating using the carbon itself as the resistance. The microwave heating equipment used gave nonuniform heating over the length of the carbon column and was not pursued further. Electric resistance, or Rintoul, heating is a commercially proven process that has been applied to the high-temperature regeneration of liquid-phase GAC in special purpose furnaces. The experimental program demonstrated that the Rintoul process can be efficiently applied to low-temperature, low energy, in-place regeneration of vapor-phase GAO. Repeated loading and regeneration of the carbon column showed no loss of adsorption capacity. Two methods of collecting TCE in a concentrated form were also successfully tested. Both processes involved recovery of the TCE in a condensate.

  6. Whole-body pharmacokinetics of HDAC inhibitor drugs, butyric acid, valproic acid and 4-phenylbutyric acid measured with carbon-11 labeled analogs by PET

    PubMed Central

    Kim, Sung Won; Hooker, Jacob M.; Otto, Nicola; Win, Khaing; Muench, Lisa; Shea, Colleen; Carter, Pauline; King, Payton; Reid, Alicia E.; Volkow, Nora D.; Fowler, Joanna S.

    2013-01-01

    The fatty acids, n-butyric acid (BA), 4-phenylbutyric acid (PBA) and valproic acid (VPA, 2-propylpentanoic acid) have been used for many years in the treatment of a variety of CNS and peripheral organ diseases including cancer. New information that these drugs alter epigenetic processes through their inhibition of histone deacetylases (HDACs) has renewed interest in their biodistribution and pharmacokinetics and the relationship of these properties to their therapeutic and side effect profile. In order to determine the pharmacokinetics and biodistribution of these drugs in primates, we synthesized their carbon-11 labeled analogues and performed dynamic positron emission tomography (PET) in six female baboons over 90 min. The carbon-11 labeled carboxylic acids were prepared by using 11CO2 and the appropriate Grignard reagents. [11C]BA was metabolized rapidly (only 20% of the total carbon-11 in plasma was parent compound at 5 min post injection) whereas for VPA and PBA 98% and 85% of the radioactivity was the unmetabolized compound at 30 min after their administration respectively. The brain uptake of all three carboxylic acids was very low (<0.006%ID/cc, BA>VPA>PBA), which is consistent with the need for very high doses for therapeutic efficacy. Most of the radioactivity was excreted through the kidneys and accumulated in the bladder. However, the organ biodistribution between the drugs differed. [11C]BA showed relatively high uptake in spleen and pancreas whereas [11C]PBA showed high uptake in liver and heart. Notably, [11C]VPA showed exceptionally high heart uptake possibly due to its involvement in lipid metabolism. The unique biodistribution of each of these drugs may be of relevance in understanding their therapeutic and side effect profile including their teratogenic effects. PMID:23906667

  7. Synthesis of a sugar-organometallic compound 1,1‧-difurfurylferrocene and its microwave preparation of carbon/iron oxide nanocomposite

    NASA Astrophysics Data System (ADS)

    Zhao, Shanyu; Cooper, Daniel C.; Xu, Haixun; Zhu, Pinghua; Suggs, J. William

    2013-01-01

    In order to synthesize a carbon-metal or metal oxide combination sphere, carbonaceous resource furfural 1 was introduced, which was nucleophilic treated with 1,1‧-dilithioferrocene 2 to form a sugar-organometallic compound: ferrocenyl monosaccharide derivative 1,1‧-difurfurylferrocene 3. 1,1‧-Difurfurylferrocene 3 can be hydrothermally treated in a microwave reactor to give 300-500 nm microspheres with the α-Fe2O3 or Fe3O4 nanocrystals formed on the surface, which may be favorable for new magnetic materials preparation or instead of iron with other metal ions, versatile carbon/metal composites will be possibly synthesized for catalysis, drug delivery and magnetic uses.

  8. Effects of heat treatment on the corrosion resistance of carbon steel coated with LaMgAl11O19 thermal barrier coatings

    NASA Astrophysics Data System (ADS)

    Huang, Liang-liang; Meng, Hui-min; Liang, Li-kang; Li, Sen; Shi, Jin-hui

    2015-10-01

    LaMgAl11O19 thermal barrier coatings (TBCs) were applied to carbon steels with a NiCoCrAlY bond coat by plasma spraying. The effects of heat treatment on the corrosion resistance of carbon steel coated with LaMgAl11O19 TBCs were investigated in 3.5wt% NaCl solution using polarization curves, electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The results show that a large number of cracks are found in the LaMgAl11O19 TBCs after the samples are heat-treated, including some through-thickness cracks. The corrosion forms of the as-sprayed and heat-treated TBCs are uniform corrosion and pitting corrosion, respectively. The as-sprayed TBCs exhibit three EIS time constants after being immersed for less than 7 d, and then a new time constant appears because of steel substrate corrosion. When the immersion time is increased to 56 d, a Warburg impedance ( W) component appears in the EIS data. The EIS data for the heat-treated TBCs exhibit only two time constants after the samples are immersed for less than 14 d, and a new time constant appears when the immersion time is increased further. The heat treatment reduces the corrosion resistance of carbon steel coated with LaMgAl11O19 TBCs. The corrosion products are primarily γ-FeOOH and Fe3O4.

  9. Air-tolerant Fabrication and Enhanced Thermoelectric Performance of n-Type Single-walled Carbon Nanotubes Encapsulating 1,1'-Bis(diphenylphosphino)ferrocene.

    PubMed

    Nonoguchi, Yoshiyuki; Iihara, Yu; Ohashi, Kenji; Murayama, Tomoko; Kawai, Tsuyoshi

    2016-09-01

    The thermally-triggered n-type doping of single-walled carbon nanotubes is demonstrated using 1,1'-bis(diphenylphosphino)ferrocene, a novel n-type dopant. Through a simple thermal vacuum process, the phosphine compounds are moderately encapsulated inside single-walled carbon nanotubes. The encapsulation into SWNTs is carefully characterized using Raman/X-ray spectroscopy and transmission electron microscopy. This easy-to-handle doping with air-stable precursors for n-type SWNTs enables the large-scale fabrication of thermoelectric materials showing an excellent power factor exceeding approximately 240 μW mK(-2) .

  10. Air-tolerant Fabrication and Enhanced Thermoelectric Performance of n-Type Single-walled Carbon Nanotubes Encapsulating 1,1'-Bis(diphenylphosphino)ferrocene.

    PubMed

    Nonoguchi, Yoshiyuki; Iihara, Yu; Ohashi, Kenji; Murayama, Tomoko; Kawai, Tsuyoshi

    2016-09-01

    The thermally-triggered n-type doping of single-walled carbon nanotubes is demonstrated using 1,1'-bis(diphenylphosphino)ferrocene, a novel n-type dopant. Through a simple thermal vacuum process, the phosphine compounds are moderately encapsulated inside single-walled carbon nanotubes. The encapsulation into SWNTs is carefully characterized using Raman/X-ray spectroscopy and transmission electron microscopy. This easy-to-handle doping with air-stable precursors for n-type SWNTs enables the large-scale fabrication of thermoelectric materials showing an excellent power factor exceeding approximately 240 μW mK(-2) . PMID:27439731

  11. Tandem carbon-carbon bond insertion and intramolecular aldol reaction of benzyne with aroylacetones: novel formation of 4,4'-disubstituted 1,1'-binaphthols.

    PubMed

    Okuma, Kentaro; Itoyama, Ryoichi; Sou, Ayumi; Nagahora, Noriyoshi; Shioj, Kosei

    2012-11-21

    An efficient route to 4-aryl-2-naphthols from arynes and aroylacetones was developed by carbon-carbon bond insertion followed by an intramolecular aldol reaction and dehydration. Benzyne derived from 2-(trimethylsilyl)phenyl triflate reacted with benzoylacetones in refluxing acetonitrile to give 4-aryl-2-naphthols and 3-aryl-1-naphthols.

  12. USGS Arctic Ocean carbon cruise 2011: field activity H-01-11-AR to collect carbon data in the Arctic Ocean, August - September 2011

    USGS Publications Warehouse

    Robbins, Lisa L.; Yates, Kimberly K.; Knorr, Paul O.; Wynn, Jonathan; Lisle, John; Buczkowski, Brian J.; Moore, Barbara; Mayer, Larry; Armstrong, Andrew; Byrne, Robert H.; Liu, Xuewu

    2013-01-01

    Carbon dioxide (CO2) in the atmosphere is absorbed at the surface of the ocean by reacting with seawater to form a weak, naturally occurring acid called carbonic acid. As atmospheric carbon dioxide increases, the concentration of carbonic acid in seawater also increases, causing a decrease in ocean pH and carbonate mineral saturation states, a process known as ocean acidification. The oceans have absorbed approximately 525 billion tons of carbon dioxide from the atmosphere, or about one-quarter to one-third of the anthropogenic carbon emissions released since the beginning of the Industrial Revolution (Sabine and others, 2004). Global surveys of ocean chemistry have revealed that seawater pH has decreased by about 0.1 units (from a pH of 8.2 to 8.1) since the 1700s due to absorption of carbon dioxide (Caldeira and Wickett, 2003; Orr and others, 2005; Raven and others, 2005). Modeling studies, based on Intergovernmental Panel on Climate Change (IPCC) CO2 emission scenarios, predict that atmospheric carbon dioxide levels could reach more than 500 parts per million (ppm) by the middle of this century and 800 ppm by the year 2100, causing an additional decrease in surface water pH of 0.3 pH units. Ocean acidification is a global threat and is already having profound and deleterious effects on the geology, biology, chemistry, and socioeconomic resources of coastal and marine habitats (Raven and others, 2005; Ruttiman, 2006). The polar and sub-polar seas have been identified as the bellwethers for global ocean acidification.

  13. Determination of δ11B by HR-ICP-MS from mass limited samples: Application to natural carbonates and water samples

    NASA Astrophysics Data System (ADS)

    Misra, Sambuddha; Owen, Robert; Kerr, Joanna; Greaves, Mervyn; Elderfield, Henry

    2014-09-01

    We present an improved method for accurate and precise determination of the boron isotopic composition (11B/10B) of carbonate and water samples using a mineral acid matrix and HR-ICP-MS. Our method for δ11B determination utilizes a micro-distillation based boron purification technique for both carbonate and seawater matrices. The micro-distillation method is characterized by low blank (⩽0.01 ng-B) and 99.8 ± 5.7% boron recovery. We also report a new ICP-MS method, performed in a hydrofluoric acid matrix, using a jet interface fitted Thermo® Element XR that consumes <3.0 ng-B per quintuplicate analyses (±0.5‰, 2σ, n = 5). A comparatively high matrix tolerance limit of ⩽50 ppb Na/K/Mg/Ca characterizes our ICP-MS method. With an extremely low procedural blank (⩽0.05 ± 0.01 ng-B) the present isotope method is optimized for rapid (∼25 samples per session) analysis of small masses of carbonates (foraminifera, corals) with low boron abundance and small volume water samples (seawater, porewater, river water). Our δ11B estimates of seawater (39.8 ± 0.5‰, 2σ, n = 30); SRM AE-120 (-20.2 ± 0.5‰, 2s, n = 33); SRM AE-121 (19.8 ± 0.4‰, 2s, n = 16); SRM AE-122 (39.6 ± 0.5‰, 2s, n = 16) are within analytical uncertainty of published values. We apply this new method to assess the impacts of laboratory handling induced sample contamination and seawater physio-chemical parameters (temperature, pH, and salinity) on marine carbonate bound δ11B by analyzing core-top planktonic foraminifera samples.

  14. Syntheses and Radiosyntheses of Two Carbon-11 Labeled Potent and Selective Radioligands for Imaging Vesicular Acetylcholine Transporter

    PubMed Central

    Padakanti, Prashanth K.; Zhang, Xiang; Li, Junfeng; Parsons, Stanley M.; Perlmutter, Joel S.; Tu, Zhude

    2015-01-01

    Purpose The vesicular acetylcholine transporter (VAChT) is a specific biomarker for imaging presynaptic cholinergic neurons. The syntheses and C-11 labeling of two potent enantiopure VAChT inhibitors are reported here. Procedures Two VAChT inhibitors, (±)-2 and (±)-6, were successfully synthesized. A chiral HPLC column was used to resolve the enantiomers from each corresponding racemic mixture for in vitro characterization. The radiosyntheses of (−)-[11C]2 and (−)-[11C]6 from the corresponding desmethyl phenol precursor was accomplished using [11C]methyl iodide or [11C]methyl triflate, respectively. Results The synthesis of (−)-[11C]2 was accomplished with 40–50 % radiochemical yield (decay-corrected), SA>480 GBq/μmol (EOB), and radiochemical purity >99 %. Synthesis of (−)-[11C]6 was accomplished with 5–10 % yield, SA>140 GBq/μmol (EOB), and radiochemical purity >97 %. The radiosynthesis and dose formulation of each tracer was completed in 55–60 min. Conclusions Two potent enantiopure VAChT ligands were synthesized and 11C-labeled with good radiochemical yield and specific activity. PMID:24875230

  15. Understanding Climate Policy Data Needs. NASA Carbon Monitoring System Briefing: Characterizing Flux Uncertainty, Washington D.C., 11 January 2012

    NASA Technical Reports Server (NTRS)

    Brown, Molly E.; Macauley, Molly

    2012-01-01

    Climate policy in the United States is currently guided by public-private partnerships and actions at the local and state levels. This mitigation strategy is made up of programs that focus on energy efficiency, renewable energy, agricultural practices and implementation of technologies to reduce greenhouse gases. How will policy makers know if these strategies are working, particularly at the scales at which they are being implemented? The NASA Carbon Monitoring System (CMS) will provide information on carbon dioxide fluxes derived from observations of earth's land, ocean and atmosphere used in state of the art models describing their interactions. This new modeling system could be used to assess the impact of specific policy interventions on CO2 reductions, enabling an iterative, results-oriented policy process. In January of 2012, the CMS team held a meeting with carbon policy and decision makers in Washington DC to describe the developing modeling system to policy makers. The NASA CMS will develop pilot studies to provide information across a range of spatial scales, consider carbon storage in biomass, and improve measures of the atmospheric distribution of carbon dioxide. The pilot involves multiple institutions (four NASA centers as well as several universities) and over 20 scientists in its work. This pilot study will generate CO2 flux maps for two years using observational constraints in NASA's state-of -the-art models. Bottom-up surface flux estimates will be computed using data-constrained land and ocean models; comparison of the different techniques will provide some knowledge of uncertainty in these estimates. Ensembles of atmospheric carbon distributions will be computed using an atmospheric general circulation model (GEOS-5), with perturbations to the surface fluxes and to transport. Top-down flux estimates will be computed from observed atmospheric CO2 distributions (ACOS/GOSAT retrievals) alongside the forward-model fields, in conjunction with an

  16. Effects of carbon and hafnium concentrations in wrought powder-metallurgy superalloys based on NASA 2B-11 alloy

    NASA Technical Reports Server (NTRS)

    Miner, R. V., Jr.

    1976-01-01

    A candidate alloy for advanced-temperature turbine engine disks, and four modifications of that alloy with various C and Hf concentrations were produced as cross-rolled disks from prealloyed powder that was hot isostatically compacted. The mechanical properties, microstructures, and phase relations of the alloys are discussed in terms of their C and Hf concentrations. A low-C and high-Hf modification of IIB-11 had the best balance of mechanical properties for service below about 750 C. Because of their finer grain sizes, none of the powder-metallurgy alloys produced had the high-temperature rupture strength of conventionally cast and wrought IIB-11.

  17. PET study of carbon-11-PK 11195 binding to peripheral type benzodiazepine sites in glioblastoma: A case report

    SciTech Connect

    Pappata, S.; Cornu, P.; Samson, Y.; Prenant, C.; Benavides, J.; Scatton, B.; Crouzel, C.; Hauw, J.J.; Syrota, A. )

    1991-08-01

    The utility of the peripheral type benzodiazepine site ligand 11C-PK 11195, for imaging human glioma in conjunction with Positron Emission Tomography, relies on a high specific binding of the tracer to tumoral peripheral type benzodiazepines sites. In a patient with glioblastoma, the authors found that 11C-PK 11195 binding was two-fold higher in the tumor than in normal gray matter and that 30% of tumoral binding could be displaced by a large excess of unlabeled drug. These findings suggest that tumoral retention of the ligand is due, in part, to specific binding.

  18. Oxidation of aromatic lithium thiolates into sulfinate salts: an attractive entry to aryl sulfones labeled with carbon-11.

    PubMed

    Martin, Claudie; Sandrinelli, Franck; Perrio, Cécile; Perrio, Stéphane; Lasne, Marie-Claire

    2006-01-01

    [reaction: see text] Aromatic 11C-sulfones were synthesized by S alkylation of lithium arenesulfinates, which are readily available from the corresponding thiols by an oxaziridine-mediated oxidation reaction with [11C]alkyl iodides in THF/H2O (4:1) at 150 degrees C. The radiosyntheses, including purification by HPLC, were completed in an average of 35 min from the end of the bombardment with 55-76% overall radiochemical yields (decay corrected). The described procedure extends the range of accessible labeling methods.

  19. The mutation DGT1-1 decreases glucose transport and alleviates carbon catabolite repression in Saccharomyces cerevisiae.

    PubMed

    Gamo, F J; Lafuente, M J; Gancedo, C

    1994-12-01

    Glucose in ethanol-glycerol mixtures inhibits growth of Saccharomyces cerevisiae mutants lacking phosphoglycerate mutase. A suppressor mutation that relieved glucose inhibition was isolated. This mutation, DGT1-1 (decreasing glucose transport), was dominant and produced pleiotropic effects even in an otherwise wild-type background. Growth of the DGT1-1 mutant in glucose was dependent on respiration, and no ethanol was detected in the medium within 7 h of glucose addition. When grown on glucose, the mutant had a reduced glucose uptake and both the low- and high-affinity transport systems were affected. In galactose-grown cells, only the high-affinity glucose transport system was detected. This system had similar kinetic characteristics in the wild type and in the mutant. Catabolite repression of several enzymes was absent in the mutant during growth in glucose but not during growth in galactose. In contrast with the wild type, the mutant grown in glucose had high transcription of the glucose transporter gene SNF3 and no transcription of HXT1 and HXT3. Expression of multicopy plasmids carrying the HXT1, HXT2, or HXT3 gene allowed partial recovery of both fermentative capacity and catabolite repression in the mutant. The results suggest that DGT1 codes for a regulator of the expression of glucose transport genes. They also suggest that glucose flux might determine the levels of molecules implicated as signals in catbolite repression.

  20. Anthropogenic carbon estimates in the North Atlantic in CMIP5 GCMs using reconstructed transient tracers (CFC-11, CFC-12, SF6).

    NASA Astrophysics Data System (ADS)

    Tudino, Tobia; Messias, Marie-Jose; Schuster, Ute; Watson, Andrew J.

    2015-04-01

    Since the beginning of the industrial revolution, atmospheric concentration of carbon dioxide has raised from 280 ppm to nearly 400 ppm. The Global Ocean has limited the consequent greenhouse effect on the climate system by taking up around 26% (2.3 ± 0.7 PgC/yr) of the carbon produced by human activities (anthropogenic carbon, Cant), mostly in key areas, such as the North Atlantic. Estimating anthropogenic carbon in the ocean is challenging because Cant cannot be measured directly, it is difficult to separate from the biggest unknown natural fraction (DIC), it is influenced by the biogeochemical cycles and the circulation in the ocean. Therefore, Cant is estimated with different methods (ΔC*, φCTO, TTD) based on carbon parameters (DIC, alkalinity, silicate, phosphate) or transient tracers observations. Here, we used CFC-11, CFC-12 and sulphur hexafluoride (SF6) measured along the subtropical North Atlantic (26° N) in 2010 as proxies for the Cantestimates. However, these transient tracer observations are sparse and few GCMs (e.g.: OCMIP project) have reported them in the outputs. Therefore, oxygen and potential temperature observations registered on 1992, 1998, 2004 and 2010 along the 26° N transect have been used, with a combined CFC-12/SF6 water masses ages trend and the CMIP5 GCM (MPI-ESM, IPSL-CM5) outputs to reconstruct transient tracers concentrations using regression models. Overall, the 2010 residual analyses confirm the validity of the statistical approach and derived values show a consistency with the tracer observations (averaged R2 > 0.9). These regression models have been used to derive Cant from 1992 to 2014, in CMIP5 GCMs (MPI-ESM, IPSL-CM5), using the reconstructed transient tracers fields with the transit-time distribution (TTD) method. Results are, finally, compared to the Cant distributions and budgets calculated, in the same area, with other methods (ΔC*, φCTO) and the Cant directly estimated from the GCMs as the difference between the

  1. L-[METHYL-{sup 11}C] Methionine Positron Emission Tomography for Target Delineation in Malignant Gliomas: Impact on Results of Carbon Ion Radiotherapy

    SciTech Connect

    Mahasittiwat, Pawinee; Mizoe, Jun-etsu Hasegawa, Azusa; Ishikawa, Hiroyuki; Yoshikawa, Kyosan; Mizuno, Hideyuki; Yanagi, Takeshi; Takagi, Ryou D.D.S.; Pattaranutaporn, Pittayapoom; Tsujii, Hirohiko

    2008-02-01

    Purpose: To assess the importance of {sup 11}C-methionine (MET)-positron emission tomography (PET) for clinical target volume (CTV) delineation. Methods and Materials: This retrospective study analyzed 16 patients with malignant glioma (4 patients, anaplastic astrocytoma; 12 patients, glioblastoma multiforme) treated with surgery and carbon ion radiotherapy from April 2002 to Nov 2005. The MET-PET target volume was compared with gross tumor volume and CTV, defined by using computed tomography/magnetic resonance imaging (MRI). Correlations with treatment results were evaluated between positive and negative extended volumes (EVs) of the MET-PET target for CTV. Results: Mean volumes of the MET-PET targets, CTV1 (defined by means of high-intensity volume on T2-weighted MRI), and CTV2 (defined by means of contrast-enhancement volume on T1-weighted MRI) were 6.35, 264.7, and 117.7 cm{sup 3}, respectively. Mean EVs of MET-PET targets for CTV1 and CTV2 were 0.6 and 2.2 cm{sup 3}, respectively. The MET-PET target volumes were included in CTV1 and CTV2 in 13 (81.3%) and 11 patients (68.8%), respectively. Patients with a negative EV for CTV1 had significantly greater survival rate (p = 0.0069), regional control (p = 0.0047), and distant control time (p = 0.0267) than those with a positive EV. Distant control time also was better in patients with a negative EV for CTV2 than those with a positive EV (p = 0.0401). Conclusions: For patients with malignant gliomas, MET-PET has a possibility to be a predictor of outcome in carbon ion radiotherapy. Direct use of MET-PET fused to planning computed tomography will be useful and yield favorable results for the therapy.

  2. Waste Biogas residue from cassava dregs as carbon source to produce Galactomyces sp. Cczu11-1 cellulase and its enzymatic saccharification.

    PubMed

    He, Yu-Cai; Gong, Lei; Liu, Feng; Lu, Ting; Qing, Qing; Wang, Li-Qun; Zhang, Yue; Gao, Feng-Ting; Wang, Xi

    2014-06-01

    In the conversion of cassava starch dregs to biogas by anaerobic fermentation, the biogas residue (BR) containing lignocellulosic materials still remained in the environment. In order to effectively utilize BR, the complexed 1-methyl-3-methylimidazolium dimethyl phosphate ([Mmim]DMP) media were used for pretreating cellulosic materials. After the optimization of pretreatment, the IL [Mmim]DMP-HCl-water (78.5:1.5:20, w/w/w) pretreament media were used for pretreating BR at 130 °C for 30 min. Furthermore, BR pretreated could be effectively saccharified by cellulase of Galactomyces sp. CCZU11-1. Moreover, BR could be used as a cheap carbon source for the production of Galactomyces sp. CCZU11-1 cellulase. After the culture optimization, the optimal culture conditions were obtained as follows: BR 5 g/L, (NH4)2SO4 5 g/L, K2HPO4 2 g/L, MgSO4 0.2 g/L, NaCl 1 g/L, PEG6000 4 g/L, pH 5.5, and culture temperature 30 °C. After the fermentation for 6 days, the FPA and CMCase were 26.2 and 52.8 U/mL, respectively. In conclusion, waste BR could be chosen as a promising feedstock for biofuels.

  3. Accumulated expression level of cytosolic glutamine synthetase 1 gene (OsGS1;1 or OsGS1;2) alter plant development and the carbon-nitrogen metabolic status in rice.

    PubMed

    Bao, Aili; Zhao, Zhuqing; Ding, Guangda; Shi, Lei; Xu, Fangsen; Cai, Hongmei

    2014-01-01

    Maintaining an appropriate balance of carbon to nitrogen metabolism is essential for rice growth and yield. Glutamine synthetase is a key enzyme for ammonium assimilation. In this study, we systematically analyzed the growth phenotype, carbon-nitrogen metabolic status and gene expression profiles in GS1;1-, GS1;2-overexpressing rice and wildtype plants. Our results revealed that the GS1;1-, GS1;2-overexpressing plants exhibited a poor plant growth phenotype and yield and decreased carbon/nitrogen ratio in the stem caused by the accumulation of nitrogen in the stem. In addition, the leaf SPAD value and photosynthetic parameters, soluble proteins and carbohydrates varied greatly in the GS1;1-, GS1;2-overexpressing plants. Furthermore, metabolite profile and gene expression analysis demonstrated significant changes in individual sugars, organic acids and free amino acids, and gene expression patterns in GS1;1-, GS1;2-overexpressing plants, which also indicated the distinct roles that these two GS1 genes played in rice nitrogen metabolism, particularly when sufficient nitrogen was applied in the environment. Thus, the unbalanced carbon-nitrogen metabolic status and poor ability of nitrogen transportation from stem to leaf in GS1;1-, GS1;2-overexpressing plants may explain the poor growth and yield.

  4. Accumulated Expression Level of Cytosolic Glutamine Synthetase 1 Gene (OsGS1;1 or OsGS1;2) Alter Plant Development and the Carbon-Nitrogen Metabolic Status in Rice

    PubMed Central

    Bao, Aili; Zhao, Zhuqing; Ding, Guangda; Shi, Lei; Xu, Fangsen; Cai, Hongmei

    2014-01-01

    Maintaining an appropriate balance of carbon to nitrogen metabolism is essential for rice growth and yield. Glutamine synthetase is a key enzyme for ammonium assimilation. In this study, we systematically analyzed the growth phenotype, carbon-nitrogen metabolic status and gene expression profiles in GS1;1-, GS1;2-overexpressing rice and wildtype plants. Our results revealed that the GS1;1-, GS1;2-overexpressing plants exhibited a poor plant growth phenotype and yield and decreased carbon/nitrogen ratio in the stem caused by the accumulation of nitrogen in the stem. In addition, the leaf SPAD value and photosynthetic parameters, soluble proteins and carbohydrates varied greatly in the GS1;1-, GS1;2-overexpressing plants. Furthermore, metabolite profile and gene expression analysis demonstrated significant changes in individual sugars, organic acids and free amino acids, and gene expression patterns in GS1;1-, GS1;2-overexpressing plants, which also indicated the distinct roles that these two GS1 genes played in rice nitrogen metabolism, particularly when sufficient nitrogen was applied in the environment. Thus, the unbalanced carbon-nitrogen metabolic status and poor ability of nitrogen transportation from stem to leaf in GS1;1-, GS1;2-overexpressing plants may explain the poor growth and yield. PMID:24743556

  5. Absolute quantitation of iodine-123 epidepride kinetics using single-photon emission tomography: comparison with carbon-11 epidepride and positron emission tomography.

    PubMed

    Almeida, P; Ribeiro, M J; Bottlaender, M; Loc'h, C; Langer, O; Strul, D; Hugonnard, P; Grangeat, P; Mazière, B; Bendriem, B

    1999-12-01

    Epidepride labelled with iodine-123 is a suitable probe for the in vivo imaging of striatal and extrastriatal dopamine D2 receptors using single-photon emission tomography (SPET). Recently, this molecule has also been labelled with carbon-11. The goal of this work was to develop a method allowing the in vivo quantification of radioactivity uptake in baboon brain using SPET and to validate it using positron emission tomography (PET). SPET studies were performed in Papio anubis baboons using 123I-epidepride. Emission and transmission measurements were acquired on a dual-headed system with variable head angulation and low-energy ultra-high resolution (LEUHR) collimation. The imaging protocol consisted of one transmission measurement (24 min, heads at 90 degrees), obtained with two sliding line sources of gadolinium-153 prior to injection of 0.21-0.46 GBq of 123I-epidepride, and 12 emission measurements starting 5 min post injection. For scatter correction (SC) we used a dual-window method adapted to 123I. Collimator blurring correction (CBC) was done by deconvolution in Fourier space and attenuation correction (AT) was applied on a preliminary (CBC) filtered back-projection reconstruction using 12 iterations of a preconditioned, regularized minimal residual algorithm. For each reconstruction, a calibration factor was derived from a uniform cylinder filled with a 123I solution of a known radioactivity concentration. Calibration and baboon images were systematically built with the same reconstruction parameters. Uncorrected (UNC) and (AT), (SC + AT) and (SC + CBC + AT) corrected images were compared. PET acquisitions using 0.11-0.44 GBq of 11C-epidepride were performed on the same baboons and used as a reference. The radioactive concentrations expressed in percent of the injected dose per 100 ml (% ID/100 ml) obtained after (SC + CBC + AT) in SPET are in good agreement with those obtained with PET and 11C-epidepride. A method for the in vivo absolute quantitation of 123

  6. Comparative study of the pharmacokinetics of carbon tetrachloride in the rat following repeated inhalation exposures of 8 and 11. 5 hr/day

    SciTech Connect

    Paustenbach, D.J.; Carlson, G.P.; Christian, J.E.; Born, G.S.

    1986-04-01

    To evaluate whether exposure to inhaled vapors for periods longer than 8 hr/day could affect the rates and routes of elimination, male Sprague-Dawley rats were repeatedly exposed to 100 ppm of radiolabeled carbon tetrachloride (/sup 14/CCl/sub 4/) in a closed-loop chamber. One group was exposed for 8 hr/day for 5 days and another group for 11.5 hr/day for 4 days. Two other groups were exposed for either 8 hr/day for 10 of 12 consecutive days or 11.5 hr/day for 7 of 10 days. The elimination of /sup 14/C activity was measured in the expired air, urine, and feces for up to 100 hr following exposure and the pharmacokinetic parameters were determined. Following 2 weeks of exposure to the 8-hr/day schedule, /sup 14/CCl/sub 4/ in the breath and /sup 14/C activity in the feces comprised 45 and 48% of the total /sup 14/C excreted, respectively. Following 2 weeks of exposure to the 11.5-hr/day schedule, the values were 32 and 62%, respectively, indicating that repeated exposure to the longer schedule altered the route of elimination of CCl/sub 4/. Regardless of the period of exposure, less than 8% of the inhaled /sup 14/CCl/sub 4/ was excreted in the urine and less than 2% was exhaled in the breath as the /sup 14/CO/sub 2/ metabolite. Approximately 97-98% of the /sup 14/C activity in the expired air was /sup 14/CCl/sub 4/. The quantities of /sup 14/C noted in the feces and urine suggest that more than 60% of the inhaled CCl/sub 4/ was metabolized. Elimination of /sup 14/CCl/sub 4/ and /sup 14/CO/sub 2/ in the breath followed a two-compartment, first-order pharmacokinetic model (r2 = 0.98). For rats exposed 8 hr/day and 11.5 hr/day for 2 weeks, the average half-lives for elimination of /sup 14/CCl/sub 4/ in the breath for the fast (alpha) and slow (beta) phases averaged 96 and 455 min, and 89 and 568 min, respectively. The average alpha and beta half-lives for elimination of /sup 14/CO/sub 2/ in the breath

  7. Evaluation of 11 terrestrial carbon-nitrogen cycle models against observations from two temperate Free-Air CO2 Enrichment studies.

    PubMed

    Zaehle, Sönke; Medlyn, Belinda E; De Kauwe, Martin G; Walker, Anthony P; Dietze, Michael C; Hickler, Thomas; Luo, Yiqi; Wang, Ying-Ping; El-Masri, Bassil; Thornton, Peter; Jain, Atul; Wang, Shusen; Warlind, David; Weng, Ensheng; Parton, William; Iversen, Colleen M; Gallet-Budynek, Anne; McCarthy, Heather; Finzi, Adrien; Hanson, Paul J; Prentice, I Colin; Oren, Ram; Norby, Richard J

    2014-05-01

    We analysed the responses of 11 ecosystem models to elevated atmospheric [CO2 ] (eCO2 ) at two temperate forest ecosystems (Duke and Oak Ridge National Laboratory (ORNL) Free-Air CO2 Enrichment (FACE) experiments) to test alternative representations of carbon (C)-nitrogen (N) cycle processes. We decomposed the model responses into component processes affecting the response to eCO2 and confronted these with observations from the FACE experiments. Most of the models reproduced the observed initial enhancement of net primary production (NPP) at both sites, but none was able to simulate both the sustained 10-yr enhancement at Duke and the declining response at ORNL: models generally showed signs of progressive N limitation as a result of lower than observed plant N uptake. Nonetheless, many models showed qualitative agreement with observed component processes. The results suggest that improved representation of above-ground-below-ground interactions and better constraints on plant stoichiometry are important for a predictive understanding of eCO2 effects. Improved accuracy of soil organic matter inventories is pivotal to reduce uncertainty in the observed C-N budgets. The two FACE experiments are insufficient to fully constrain terrestrial responses to eCO2 , given the complexity of factors leading to the observed diverging trends, and the consequential inability of the models to explain these trends. Nevertheless, the ecosystem models were able to capture important features of the experiments, lending some support to their projections.

  8. Encapsulated gadolinium and dysprosium ions within ultra-short carbon nanotubes for MR microscopy at 11.75 and 21.1 T.

    PubMed

    Rosenberg, Jens T; Cisneros, Brandon T; Matson, Michael; Sokoll, Michelle; Sachi-Kocher, Afi; Bejarano, Fabian Calixto; Wilson, Lon J; Grant, Samuel C

    2014-01-01

    Single-walled carbon nanotubes (SWNTs) have gained interest for their biocompatibility and multifunctional properties. Ultra-short SWNTs (US-tubes) have demonstrated high proton relaxivity when encapsulating gadolinium ions (Gd(3+)) at clinical field strengths. At higher field strengths, however, Gd(3+) ions demonstrate decreased proton relaxation properties while chemically similar dysprosium ions (Dy(3+)) improve relaxation properties. This report investigates the first use of Gd(3+) and Dy(3+) ions within US-tubes (GNTs and DNTs, respectively) at ultra-high magnetic field (21.1 T). Both agents are compared in solution and as an intracellular contrast agent labeling a murine microglia cell line (Bv2) immobilized in a tissue-mimicking agarose phantom using two high magnetic fields: 21.1 and 11.75 T. In solution at 21.1 T, results show excellent transverse relaxation; DNTs outperformed GNTs as a T(2) agent with measured r(2)/r(1) ratios of 247 and 47, respectively. Additionally, intracellular DNTs were shown to be a better T(2) agent than GNTs with higher contrast percentages and contrast-to-noise ratios. As such, this study demonstrates the potential of DNTs at high magnetic fields for cellular labeling and future in vivo, MRI-based cell tracking.

  9. Combined δ11B, δ13C, and δ18O analyses of coccolithophore calcite constrains the response of coccolith vesicle carbonate chemistry to CO2-induced ocean acidification

    NASA Astrophysics Data System (ADS)

    Liu, Yi-Wei; Tripati, Robert; Aciego, Sarah; Gilmore, Rosaleen; Ries, Justin

    2016-04-01

    Coccolithophorid algae play a central role in the biological carbon pump, oceanic carbon sequestration, and in marine food webs. It is therefore important to understand the potential impacts of CO2-induced ocean acidification on these organisms. Differences in the regulation of carbonate chemistry, pH, and carbon sources of the intracellular compartments where coccolith formation occurs may underlie the diverse calcification and growth responses to acidified seawater observed in prior experiments. Here we measured stable isotopes of boron (δ11B), carbon (δ13C) and oxygen (δ18O) within coccolith calcite, and δ13C of algal tissue to constrain carbonate system parameters in two strains of Pleurochrysis carterae (P. carterae). The two strains were cultured under variable pCO2, with water temperature, salinity, dissolved inorganic carbon (DIC), and alkalinity monitored. Notably, PIC, POC, and PIC/POC ratio did not vary across treatments, indicating that P. carterae is able to calcify and photosynthesize at relatively constant rates irrespective of pCO2 treatment. The δ11B data indicate that mean pH at the site of coccolith formation did not vary significantly in response to elevated CO2. These results suggest that P. carterae regulates calcifying vesicle pH, even amidst changes in external seawater pH. Furthermore, δ13C and δ18O data suggest that P. carterae may utilize carbon from a single internal DIC pool for both calcification and photosynthesis, and that a greater proportion of dissolved CO2 relative to HCO3- enters the internal DIC pool under acidified conditions. These results suggest that P. carterae is able to calcifyand photosynthesize at relatively constant rates across pCO2 treatments by maintaining pH homeostasis at their site of calcification and utilizing a greater proportion of aqueous CO2.

  10. Combined δ11B, δ13C, and δ18O analyses of coccolithophore calcite constrains the response of coccolith vesicle carbonate chemistry to CO2-induced ocean acidification

    NASA Astrophysics Data System (ADS)

    Liu, Yi-Wei; Tripati, Robert; Aciego, Sarah; Gilmore, Rosaleen; Ries, Justin

    2016-04-01

    Coccolithophorid algae play a central role in the biological carbon pump, oceanic carbon sequestration, and in marine food webs. It is therefore important to understand the potential impacts of CO2-induced ocean acidification on these organisms. Differences in the regulation of carbonate chemistry, pH, and carbon sources of the intracellular compartments where coccolith formation occurs may underlie the diverse calcification and growth responses to acidified seawater observed in prior experiments. Here we measured stable isotopes of boron (δ11B), carbon (δ13C) and oxygen (δ18O) within coccolith calcite, and δ13C of algal tissue to constrain carbonate system parameters in two strains of Pleurochrysis carterae (P. carterae). The two strains were cultured under variable pCO2, with water temperature, salinity, dissolved inorganic carbon (DIC), and alkalinity monitored. Notably, PIC, POC, and PIC/POC ratio did not vary across treatments, indicating that P. carterae is able to calcify and photosynthesize at relatively constant rates irrespective of pCO2 treatment. The δ11B data indicate that mean pH at the site of coccolith formation did not vary significantly in response to elevated CO2. These results suggest that P. carterae regulates calcifying vesicle pH, even amidst changes in external seawater pH. Furthermore, δ13C and δ18O data suggest that P. carterae may utilize carbon from a single internal DIC pool for both calcification and photosynthesis, and that a greater proportion of dissolved CO2 relative to HCO3‑ enters the internal DIC pool under acidified conditions. These results suggest that P. carterae is able to calcifyand photosynthesize at relatively constant rates across pCO2 treatments by maintaining pH homeostasis at their site of calcification and utilizing a greater proportion of aqueous CO2.

  11. Evidence for human thromboxane receptor heterogeneity using a novel series of 9,11-cyclic carbonate derivatives of prostaglandin F2 alpha.

    PubMed Central

    Krauss, A. H.; Woodward, D. F.; Gibson, L. L.; Protzman, C. E.; Williams, L. S.; Burk, R. M.; Gac, T. S.; Roof, M. B.; Abbas, F.; Marshall, K.; Senior, J.

    1996-01-01

    1. The pharmacological activity of a novel series of 9,11-cyclic carbonate derivatives of prostaglandin F2 alpha (PGF2 alpha) was investigated in various isolated smooth muscle preparations possessing different prostanoid receptor subtypes as well as in human platelets. Since subdivision of thromboxane (TP-) receptors into vascular/smooth muscle and platelet subtypes is a controversial subject, our studies included a human smooth muscle preparation (myometrium) in addition to the widely used rat aorta and human platelets as TP-receptor preparations. 2. Two members of that series, AGN191976 and AGN192093 were found to be highly potent and selective thromboxane-mimetics. AGN191976 and AGN192093 contracted isolated tissues of the rat thoracic aorta with EC50 values of 0.32 +/- 0.08 and 1.30 +/- 0.53 nM, respectively. Both agonists were at least 10 times more potent than the benchmark TP-agonist, U-46619, in this preparation, whilst being at least 500 times less potent at other prostanoid receptors (DP, EP1, EP3, FP, IP) in vitro. 3. In human myometrial strips from pregnant and non-pregnant donors, both AGN191976 and AGN192093 were potent contractile agonists. The rank order of potency in myometrium of AGN191976 > AGN192093 > U-46619 correlated well with that in the rat aorta. In human platelet-rich plasma (PRP), however, AGN191976 had potent proaggregatory activity (EC50 = 16.3 +/- 1.4 nM), which is a TP-receptor-mediated event, whereas AGN192093 was a much weaker agonist (EC50 = 37.9 +/- 2.0 microM). AGN192093 did not behave as an antagonist in the platelets, since it did not antagonize platelet aggregation induced by ADP, arachidonic acid, U-46619 or AGN191976. In human washed platelets, the activity profile of AGN191976 (EC50 = 4.15 +/- 0.52 nM) and AGN192093 (no aggregation up to 10 microM) was similar to that obtained in PRP. 4. The involvement of TP-receptors was verified with the potent TP-antagonist, SQ29548. SQ29548 (0.1 microM in myometrium; 1 microM in

  12. Soil carbon and nitrogen cycling and storage throughout the soil profile in a sweetgum plantation after 11 years of CO2-enrichment

    SciTech Connect

    Iversen, Colleen M; Keller, Dr. Jason K.; Garten Jr, Charles T; Norby, Richard J

    2012-01-01

    Increased partitioning of carbon (C) to fine roots under elevated [CO2], especially deep in the soil profile, could alter soil C and nitrogen (N) cycling in forests. After more than 11 years of free-Air CO2 enrichment in a Liquidambar styraciflua L. (sweetgum) plantation in Oak Ridge, TN, USA, greater inputs of fine roots resulted in the incorporation of new C (i.e., C with a depleted 13C) into root-derived particulate organic matter (POM) pools to 90-cm depth. Even though production in the sweetgum stand was limited by soil N availability, soil C and N content increased over time, and were greater throughout the soil profile under elevated [CO2] at the conclusion of the experiment. However, greater C inputs under elevated [CO2] did not result in increased net N immobilization or C mineralization rates in long-term laboratory incubations, and did not appear to prime the decomposition of older SOM. The 13CO2 of the C mineralized from the incubated soil closely tracked the 13C of the labile POM pool in the elevated [CO2] treatment, especially in shallower soil, and did not indicate the decomposition of older (i.e., pre-experiment) SOM. While potential C mineralization rates were positively and linearly related to total soil organic matter (SOM) C content in the top 30 cm of soil, this relationship did not hold in deeper soil. Taken together with an increased mean residence time of C in deeper soil pools, these findings indicate that C inputs from relatively deep roots under elevated [CO2] may have increased potential for long-term storage. Expanded representation of biogeochemical cycling throughout the soil profile may improve model projections of future forest responses to rising atmospheric [CO2].

  13. Carbon Dioxide, Hydrographic, and Chemical Data Obtained During the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16S_2005 (11 January - 24 February, 2005)

    SciTech Connect

    Kozyr, Alex

    2006-08-30

    This report presents methods, and analytical and quality control procedures for salinity, oxygen, nutrient, inorganic carbon, organic carbon, chlorofluorocarbon (CFC), and bomb 14C system parameters performed during the A16S_2005 cruise, which took place from January 11 to February 24, 2005, aboard research vessel (R/V) Ronald H. Brown under the auspices of the National Oceanic and Atmospheric Administration (NOAA). The R/V Ronald H. Brown departed Punta Arenas, Chile, on January 11, 2005, and ended its cruise in Fortaleza, Brazil, on February 24, 2005. The research conducted was one of a series of repeat hydrography sections jointly funded by NOAA and the National Science Foundation as part of the CLIVAR/CO2/repeat hydrography/tracer program. Samples were taken from 36 depths at 121 stations. The data presented in this report include the analyses of water samples for total inorganic carbon (TCO2), fugacity of CO2 (fCO2), total alkalinity (TALK), pH, dissolved organic carbon (DOC), CFC, 14C, hydrographic, and other chemical measurements. The R/V Ronald H. Brown A16S_2005 data set is available free of charge as a numeric data package (NDP) from the Carbon Dioxide Information Analysis Center (CDIAC). The NDP consists of the oceanographic data files and this printed documentation, which describes the procedures and methods used to obtain the data.

  14. The effect of interstitial carbon on the mechanical properties and dislocation substructure evolution in Fe40.4Ni11.3Mn34.8Al7.5Cr6 high entropy alloys

    DOE PAGES

    Wang, Zhangwei; Baker, Ian; Cai, Zhonghou; Chen, Si; Poplawsky, Jonathan D.; Guo, Wei

    2016-09-01

    A systematic study of the effects of up to 1.1 at. % carbon on the mechanical properties and evolution of the dislocation substructure in a series of a high entropy alloys (HEA) based on Fe40.4Ni11.3Mn34.8Al7.5Cr6 is presented. Transmission electron microscopy (TEM), synchrotron X-ray diffraction (XRD) and atom probe tomography (APT) were used to show that all the alloys are single-phase f.c.c. random solid solutions. The lattice constant, determined from synchrotron XRD measurements, increases linearly with increasing carbon concentration, which leads to a linear relationship between the yield strength and the carbon concentration. The dislocation substructures, as determined by a TEM,more » show a transition from wavy slip to planar slip and, at higher strains, and from cell-forming structure (dislocations cells, cell blocks and dense dislocation walls) to non-cell forming structure (Taylor lattice, microbands and domain boundaries) with the addition of carbon, features related to the increase in lattice friction stress. The stacking fault energy (measured via weak-beam imaging of the separation of dislocation partials) decreases with increasing carbon content, which also contributes to the transition from wavy slip to planar slip. The formation of non-cell forming structure induced by carbon leads to a high degree of strain hardening and a substantial increase in the ultimate tensile strength. In conclusion, the consequent postponement of necking due to the high strain hardening, along with the plasticity accommodation arising from the formation of microbands and domain boundaries, result in an increase of ductility due to the carbon addition.« less

  15. 1,1-Carboboration.

    PubMed

    Kehr, Gerald; Erker, Gerhard

    2012-02-11

    The use of very electrophilic boranes RB(C(6)F(5))(2) widens the scope of the 1,1-carboboration reaction substantially. Simple terminal alkynes HC≡CR undergo this reaction with the RB(C(6)F(5))(2) reagents rapidly under mild conditions to give high yields of very useful new alkenylborane products. Even internal alkynes RC≡CR undergo 1,1-carboboration with the RB(C(6)F(5))(2) reagents to provide a novel way of carbon-carbon σ-bond activation. Variants of these reactions involving phosphorus substituted alkynes and more complex bisalkynyl main group and transition metal substrates give rise to the formation of very interesting functionalized metallacyclic products upon treatment with RB(C(6)F(5))(2) reagents by means of reaction sequences involving selective 1,1-carboboration steps. PMID:22116402

  16. Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C10H22O5 2,5,8,11,14-Pentaoxapentadecane (VMSD1211, LB4862_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C10H22O5 2,5,8,11,14-Pentaoxapentadecane (VMSD1211, LB4862_V)' providing data from direct low-pressure dilatometric measurement of molar excess volume at variable mole fraction and constant temperature.

  17. Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C10H22O5 2,5,8,11,14-Pentaoxapentadecane (VMSD1112, LB4865_V)

    NASA Astrophysics Data System (ADS)

    Cibulka, I.; Fontaine, J.-C.; Sosnkowska-Kehiaian, K.; Kehiaian, H. V.

    This document is part of Subvolume C 'Binary Liquid Systems of Nonelectrolytes III' of Volume 26 'Heats of Mixing, Vapor-Liquid Equilibrium, and Volumetric Properties of Mixtures and Solutions' of Landolt-Börnstein Group IV 'Physical Chemistry'. It contains the Chapter 'Volumetric Properties of the Mixture Dimethyl carbonate C3H6O3 + C10H22O5 2,5,8,11,14-Pentaoxapentadecane (VMSD1112, LB4865_V)' providing data by calculation of mass density in the single-phase region(s) from low-pressure dilatometric measurements of the molar excess volume at variable mole fraction and constant temperature.

  18. Cross sections for neutron-producing reactions induced by 14. 1 MeV neutrons incident on /sup 6/Li, /sup 7/Li, /sup 10/B, /sup 11/B, and carbon

    SciTech Connect

    Drosg, M.; Lisowski, P.W.; Drake, D.M.; Hardekopf, R.A.; Muellner, M.

    1988-10-01

    Using the time-of-flight technique, we have measured neutron emission spectra for /sup 6/Li, /sup 7/Li, /sup 10/B, /sup 11/B and carbon at an incident neutron energy of 14.1 MeV and at 10 angles between 30/degree/ and 143/degree/. Double differential cross sections and their integrated values have been extracted and are presented in tables and graphs. The nonelastic portion of the neutron emission spectra is noticeably higher than expected which may be due to uncertainties in the input library (ENDF/B-IV) used in the Monte Carlo correction for multiple scattering. In particular, the library for /sup 11/B appears to be very unrealistic with an integrated elastic cross section which should be higher by 50%. 20 refs., 1 fig., 12 tabs.

  19. Effect of an 11. 5-hr/day exposure schedule on the distribution and toxicity of inhaled carbon tetrachloride in the rat

    SciTech Connect

    Paustenbach, D.J.; Christian, J.E.; Carlson, G.P.; Born, G.S.

    1986-04-01

    This study evaluated the differences in toxicity and tissue distribution for 16 groups of male rats repeatedly exposed to 100 ppm of /sup 14/CCl/sub 4/ vapors for 8 or 11.5 hr/day for periods of 1 to 10 days. Serum sorbitol dehydrogenase (SDH) was also evaluated for its sensitivity at detecting CCl/sub 4/-induced hepatotoxicity. Following 1, 2, 3, 4, 5, 7, 11, and 14 days, one group of rats from each exposure schedule was sacrificed and /sup 14/C activity in seven tissues and serum SDH levels were measured. To compare the effects of CCl/sub 4/ on the liver and kidney following repeated exposure to the two schedules, one group of rats was exposed for 8 hr/day for 10 of 12 consecutive days and another for 11.5 hr/day for 7 of 12 consecutive days so that each group received essentially the same dose (8000 ppm-hr) of CCl/sub 4/. The 11.5-hr/day exposure schedule, compared to rats exposed 8-hr/day, produced minor changes in the distribution and concentration of /sup 14/C (CCl/sub 4/ equivalents) in various tissues. Following 1 and 2 weeks of exposure to either schedule, the fat, liver, lungs, and adrenals had the highest concentration of CCl/sub 4/ equivalents. There were no significant differences in CCl/sub 4/-induced hepatotoxicity or nephrotoxicity between rats exposed to the two schedules following either 1 or 2 weeks of exposure as measured by histopathology. In contrast, rats exposed 11.5 hr/day had significantly higher SDH levels than those exposed to the 8-hr/day schedule; thus suggesting that the 11.5-hr schedule did produce a measurably greater degree of hepatotoxicity, although it was too subtle to detect pathologically. Rats exposed for a fourth and fifth day during the second week of the 11.5-hr schedule had a significantly greater concentration of /sup 14/C activity in the fat than rats exposed to the 8-hr/day schedule.

  20. Fabrication of very-low-density, high-stiffness carbon fiber/aluminum hybridized composite with ultra-low density and high stiffness (M-11)

    NASA Technical Reports Server (NTRS)

    Suzuki, Tomoo

    1993-01-01

    Fabrication of a composite material with ultra-low density and high stiffness in microgravity is the objective of the investigation. The composite structure to be obtained is a random three-dimensional array of high modulus, short carbon fibers bonded at contact points by an aluminum alloy coated on the fibers. The material is highly porous and thus has a very low density. The motivation toward the investigation, simulation experiments, choice of the component materials, and on-flight experiment during ballistic trajectory of a NASDA rocket, are described.

  1. In vivo visualization of alpha-synuclein deposition by carbon-11-labelled 2-[2-(2-dimethylaminothiazol-5-yl)ethenyl]-6-[2-(fluoro)ethoxy]benzoxazole positron emission tomography in multiple system atrophy.

    PubMed

    Kikuchi, Akio; Takeda, Atsushi; Okamura, Nobuyuki; Tashiro, Manabu; Hasegawa, Takafumi; Furumoto, Shozo; Kobayashi, Michiko; Sugeno, Naoto; Baba, Toru; Miki, Yasuo; Mori, Fumiaki; Wakabayashi, Koichi; Funaki, Yoshihito; Iwata, Ren; Takahashi, Shoki; Fukuda, Hiroshi; Arai, Hiroyuki; Kudo, Yukitsuka; Yanai, Kazuhiko; Itoyama, Yasuto

    2010-06-01

    The histopathological hallmark of multiple system atrophy is the appearance of intracellular inclusion bodies, named glial cytoplasmic inclusions, which are mainly composed of alpha-synuclein fibrils. In vivo visualization of alpha-synuclein deposition should be used for the diagnosis and assessment of therapy and severity of pathological progression in multiple system atrophy. Because 2-[2-(2-dimethylaminothiazol-5-yl)ethenyl]-6-[2-(fluoro)ethoxy] benzoxazole could stain alpha-synuclein-containing glial cytoplasmic inclusions in post-mortem brains, we compared the carbon-11-labelled 2-[2-(2-dimethylaminothiazol-5-yl)ethenyl]-6-[2-(fluoro)ethoxy] benzoxazole positron emission tomography findings of eight multiple system atrophy cases to those of age-matched normal controls. The positron emission tomography data demonstrated high distribution volumes in the subcortical white matter (uncorrected P < 0.001), putamen and posterior cingulate cortex (uncorrected P < 0.005), globus pallidus, primary motor cortex and anterior cingulate cortex (uncorrected P < 0.01), and substantia nigra (uncorrected P < 0.05) in multiple system atrophy cases compared to the normal controls. They were coincident with glial cytoplasmic inclusion-rich brain areas in multiple system atrophy and thus, carbon-11-labelled 2-[2-(2-dimethylaminothiazol-5-yl)ethenyl]-6-[2-(fluoro)ethoxy] benzoxazole positron emission tomography is a promising surrogate marker for monitoring intracellular alpha-synuclein deposition in living brains.

  2. Spectroelectrochemical Study of Carbon Monoxide and Ethanol Oxidation on Pt/C, PtSn(3:1)/C and PtSn(1:1)/C Catalysts.

    PubMed

    Rizo, Rubén; Lázaro, María Jesús; Pastor, Elena; García, Gonzalo

    2016-09-12

    PtSn-based catalysts are one of the most active materials toward that contribute ethanol oxidation reaction (EOR). In order to gain a better understanding of the Sn influence on the carbon monoxide (principal catalyst poison) and ethanol oxidation reactions in acidic media, a systematic spectroelectrochemical study was carried out. With this end, carbon-supported PtSnx (x = 0, 1/3 and 1) materials were synthesized and employed as anodic catalysts for both reactions. In situ Fourier transform infrared spectroscopy (FTIRS) and differential electrochemical mass spectrometry (DEMS) indicate that Sn diminishes the amount of bridge bonded CO (COB) and greatly improves the CO tolerance of Pt-based catalysts. Regarding the effect of Sn loading on the EOR, it enhances the catalytic activity and decreases the onset potential. FTIRS and DEMS analysis indicate that the C-C bond scission occurs at low overpotentials and at the same potential values regardless of the Sn loading, although the amount of C-C bond breaking decreases with the rise of Sn in the catalytic material. Therefore, the elevated catalytic activity toward the EOR at PtSn-based electrodes is mainly associated with the improved CO tolerance and the incomplete oxidation of ethanol to form acetic acid and acetaldehyde species, causing the formation of a higher amount of both C2 products with the rise of Sn loading.

  3. Spectroelectrochemical Study of Carbon Monoxide and Ethanol Oxidation on Pt/C, PtSn(3:1)/C and PtSn(1:1)/C Catalysts.

    PubMed

    Rizo, Rubén; Lázaro, María Jesús; Pastor, Elena; García, Gonzalo

    2016-01-01

    PtSn-based catalysts are one of the most active materials toward that contribute ethanol oxidation reaction (EOR). In order to gain a better understanding of the Sn influence on the carbon monoxide (principal catalyst poison) and ethanol oxidation reactions in acidic media, a systematic spectroelectrochemical study was carried out. With this end, carbon-supported PtSnx (x = 0, 1/3 and 1) materials were synthesized and employed as anodic catalysts for both reactions. In situ Fourier transform infrared spectroscopy (FTIRS) and differential electrochemical mass spectrometry (DEMS) indicate that Sn diminishes the amount of bridge bonded CO (COB) and greatly improves the CO tolerance of Pt-based catalysts. Regarding the effect of Sn loading on the EOR, it enhances the catalytic activity and decreases the onset potential. FTIRS and DEMS analysis indicate that the C-C bond scission occurs at low overpotentials and at the same potential values regardless of the Sn loading, although the amount of C-C bond breaking decreases with the rise of Sn in the catalytic material. Therefore, the elevated catalytic activity toward the EOR at PtSn-based electrodes is mainly associated with the improved CO tolerance and the incomplete oxidation of ethanol to form acetic acid and acetaldehyde species, causing the formation of a higher amount of both C2 products with the rise of Sn loading. PMID:27626404

  4. Inorganic and Organic Carbon, Nutrient, and Oxygen Data from the R/V Ronald H. Brown Repeat Hydrography Cruise in the Atlantic Ocean: CLIVAR CO2 Section A16N_2003a (4 June-11 August, 2003)

    SciTech Connect

    Kozyr, Alex

    2005-08-30

    This report presents methods and analytical and quality control procedures for nutrient, oxygen, and inorganic carbon system parameters performed during the A16N_2003a cruise, which took place from June 4 to August 11, 2003 aboard NOAA Ship R/V Ronald H. Brown under auspices of the National Oceanic and Atmospheric Administration (NOAA). The first hydrographic leg (June 19–July 10) was from Reykjavik, Iceland, to Funchal, Madeira, Portugal along the 20°W meridian, and the second leg (July 15–August 11) continued operations from Funchal, Portugal to Natal, Brazil, on a track southward and ending at 6°S, 25°W. The research was the first in a decadal series of repeat hydrography sections jointly funded by NOAA and the National Science Foundation (NSF) as part of the CLIVAR/CO2/hydrography/tracer program. Samples were taken from up to 34 depths at 150 stations. The data presented in this report includes the analyses of water samples for total inorganic carbon (TCO2), fugacity of CO2 (fCO2), total alkalinity (TALK), pH, nitrate (NO3), nitrite (NO2), phosphate (PO4), silicate (SiO4), and dissolved oxygen (O2). The R/V Ronald H. Brown A16N_2003a data set is available free of charge as a numeric data package (NDP) from the Carbon Dioxide Information Analysis Center (CDIAC). The NDP consists of the oceanographic data files and this printed documentation, which describes the procedures and methods used to obtain the data.

  5. Demonstration of the carbon-sulfur bond targeted desulfurization of benzothiophene by thermophilic Paenibacillus sp. strain A11-2 capable of desulfurizing dibenzothiophene.

    PubMed

    Konishi, J; Onaka, T; Ishii, Y; Suzuki, M

    2000-06-15

    Paenibacillus sp. strain A11-2, which had been primarily isolated as a bacterial strain capable of desulfurizing dibenzothiophene to produce 2-hydroxybiphenyl at high temperatures, was found to desulfurize benzothiophene more efficiently than dibenzothiophene. The desulfurized product was identified as o-hydroxystyrene by GC-MS and 1H-NMR analysis. Benzothiophene was assumed to be degraded in a way analogous to the 4S pathway, which has been well-known as a mode of dibenzothiophene degradation. These results suggest that benzothiophene desulfurization may share at least partially the reaction mechanism with dibenzothiophene desulfurization.

  6. Evaluation of surface energy and carbon fluxes within a large wind farm during the CWEX-10/11 Crop Wind-energy EXperiments

    NASA Astrophysics Data System (ADS)

    Rajewski, D. A.; Takle, E. S.; Prueger, J. H.; Oncley, S.; Horst, T. W.; Pfeiffer, R.; Hatfield, J.; Spoth, K. K.; Doorenbos, R.

    2012-12-01

    The Crop Wind-energy EXperiment conducted in summer 2010 (very moist conditions) and summer 2011 (abnormally dry) included measurements of wind speed, temperature, relative humidity, turbulence kinetic energy, H2O, and CO2 at stations north and south of a line of turbines at the southwest edge of a large-scale 200-turbine wind farm (prevailing wind from the south). In contrast to previous studies that have reported turbine influences on surface wind speed and temperature, this report focuses on scalar fluxes of heat, H2O, and CO2. From previous measurements in agricultural fields we recognize the importance of non-turbine factors in analysis of the flux differences: variability of soil characteristics, moisture content, crop cultivar, management practices, planting dates, etc., which can create differences in what looks like a uniform field of maize (corn). We conceptualize the influences of turbines at canopy height at a given location in the field to arise from (1) wakes of reduced wind speed and turbulence conditions different from ambient that intersect the surface, (2) wakes that are passing overhead and interrupt the ambient turbulence that scales with height, or (3) changes in static pressure upwind and downwind of lines of turbines that create small-scale pressure gradients, localized flows, and changes to the vertical exchange of scalar variables. The turbine SCADA wind speed and wind direction provided by the wind farm operator facilitated our comparison of surface fluxes upwind and downwind as wakes moved laterally throughout the day and night. We report multiple levels of evidence that wind turbines increase vertical exchange of carbon dioxide and water vapor over the canopy. Latent heat and carbon fluxes are responsive to slight changes in the turbine wake position, and the flux differences are maximized when the periphery of the wake edge is above the station. The flux stations north of the turbine line report a larger net ecosystem exchange

  7. Properties of carbon-based structures synthesized in nuclear reactions induced by bremsstrahlung γ quanta with threshold energy of 10 MeV at helium pressure of 1.1 kbar

    NASA Astrophysics Data System (ADS)

    Didyk, A. Yu.; Wiśniewski, R.

    2016-07-01

    Helium gas with an initial pressure of about 1.1 kbar inside a high-pressure chamber (HeHPC) has been irradiated by bremsstrahlung γ quanta with a threshold energy of 10 MeV for 1.0 × 105 s produced by an electron-beam current of 22-24 μA. After opening the HeHPC, the residual pressure of helium is equal to 430 bar. Synthesized black foils with a variety of other objects are found inside the HeHPC. They are located on the inner surfaces of the reaction chamber made of high-purity copper (99.99%), the entrance the window of γ quanta made of beryllium bronze and a copper container of nuclear and chemical reaction products. Elemental analysis with the use of scanning electron microscopy and X-ray microprobe analysis has revealed that the foils contain predominantly carbon and small quantities of other elements from carbon to iron. The results are in good agreement with the cycle of investigations of the authors devoted to the γ-quanta irradiation of dense hydrogen and helium gases in the presence (absence) of metals in a reaction chamber.

  8. The carbon-based structures synthesized through nuclear reactions in helium at 1.1 kbar pressure under irradiation with braking γ-rays of 10 MeV threshold energy

    NASA Astrophysics Data System (ADS)

    Didyk, A. Yu.; Wisniewski, R.; Wilczynska-Kitowska, T.

    2015-01-01

    A helium high-pressure chamber (HeHPC), made from beryllium bronze, filled with gaseous helium at an initial pressure of about 1.1 kbar was irradiated by braking γ-rays of 10 MeV threshold energy during 1.0×105 \\text{s} at an electron beam current 22\\text-24 μ \\text{A} . Before opening of the chamber, the residual pressure inside was equal to 430 bar. Synthesized foils of black colour and other multiple objects were found inside the HeHPC at the inner surfaces of the reaction chamber made of high-purity copper, at the entrance window for γ-rays of beryllium bronze, and at the copper collector of nuclear and chemical reaction products. The element analysis using scanning electron microscopy (SEM) and microprobe roentgen analysis (MPRA) allowed us to establish that the foils were predominantly made of carbon and smaller quantities of other elements from carbon to iron. The developed approach agrees well with a series of studies carried out by the authors where dense hydrogen and deuterium gases are acted on by γ-rays in the presence or absence of metals in the reaction chamber.

  9. Carbon dioxide, hydrographic, and chemical data obtained during the R/V Meteor Cruise 11/5 in the South Atlantic and Northern Weddell Sea areas (WOCE sections A-12 and A-21)

    SciTech Connect

    Chipman, D.W.; Takahashi, T.; Breger, D.; Sutherland, S.C.; Kozyr, A. |; Gaslightwala, A.F. |

    1994-07-01

    This document presents the procedures and methods used to obtain carbon dioxide (CO{sub 2}), hydrographic, and chemical data during R/V Meteor Expedition 11/5 in the South Atlantic Ocean, including the Drake Passage; the Northern Weddell Sea; and the Eastern South Atlantic Ocean. This cruise was conducted as part of the World Ocean Circulation Experiment (WOCE). The cruise started from Ushuaia, Argentina, on January 23, 1990, and ended at Capetown, South Africa on March 8, 1990. Samples were collected at 78 stations that covered the Drake Passage; the Northern Weddell Sea; a section along the 58 W parallel; and two segmented S-N sections between the Northern Weddell Sea and Capetown, South Africa. Measurements taken at WOCE sections A-12 and A-21 included pressure, temperature, salinity measured by the Conductivity, Temperature and Depth sensor (CTD); bottle salinity; oxygen; phosphate; nitrate; nitrate; silicate; total carbon concentration (TCO{sub 2}); and partial pressure of CO{sub 2} (pCO{sub 2}) measured at 20 C. In addition, potential density at 0 decibar (dbar) and potential temperature were calculated from the measured variables. The TCO{sub 2} concentration in seawater samples was measured using a coulometer with an estimated precision of approximately {+-} {mu}mol/kg.

  10. The effect of carbon doping on the upper critical field (Hc2) and resistivity of MgB2 by using sucrose (C12H22O11) as the carbon source

    NASA Astrophysics Data System (ADS)

    Zhang, Y.; Zhou, S. H.; Lu, C.; Konstantinov, K.; Dou, S. X.

    2009-01-01

    In this work, sucrose was doped into MgB2 samples to act as a carbon source. The sintering temperature varied from 850 to 1050 °C. The effects of sucrose doping and sintering temperature on the lattice parameters, microstrain, critical temperature (Tc), resistivity, and upper critical field (Hc2) have been investigated in detail. It has been found that sucrose doping results in a small depression in Tc and high resistivity, while the Hc2 performance is improved. The best performance was shown in the sucrose-doped sample sintered at 850 °C. The reason for the enhancement of Hc2 is likely to be disorder caused by C substitution for B and/or diffusion of C atoms in the MgB2 lattice as interstitial atoms.

  11. E11 in 11D

    NASA Astrophysics Data System (ADS)

    Tumanov, Alexander G.; West, Peter

    2016-07-01

    We construct the non-linear realisation of the semi-direct product of E11 and its vector representation in eleven dimensions and find the dynamical equations it predicts at low levels. These equations are completely determined by the non-linear realisation and when restricted to contain only the usual fields of supergravity and the usual spacetime we find precisely the equations of motion of eleven dimensional supergravity. This paper extends the results announced in arxiv:hep-th/1512.01644 and in particular it contains the contributions to the equations of motion that involve derivatives with respect to the level one generalised coordinates.

  12. 43 CFR 11.11 - Purpose.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false Purpose. 11.11 Section 11.11 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.11... natural resource damages. The results of an assessment performed by a Federal or State natural...

  13. 43 CFR 11.11 - Purpose.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false Purpose. 11.11 Section 11.11 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.11... natural resource damages. The results of an assessment performed by a Federal or State natural...

  14. 6 CFR 11.11 - Compromise.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 6 Domestic Security 1 2012-01-01 2012-01-01 false Compromise. 11.11 Section 11.11 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY CLAIMS § 11.11 Compromise. DHS may compromise a debt in accordance with the provisions of 31 CFR part 902. The Chief Financial Officer...

  15. 6 CFR 11.11 - Compromise.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 6 Domestic Security 1 2011-01-01 2011-01-01 false Compromise. 11.11 Section 11.11 Domestic Security DEPARTMENT OF HOMELAND SECURITY, OFFICE OF THE SECRETARY CLAIMS § 11.11 Compromise. DHS may compromise a debt in accordance with the provisions of 31 CFR part 902. The Chief Financial Officer...

  16. 11 CFR 9032.11 - State.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 11 Federal Elections 1 2011-01-01 2011-01-01 false State. 9032.11 Section 9032.11 Federal Elections FEDERAL ELECTION COMMISSION PRESIDENTIAL ELECTION CAMPAIGN FUND: PRESIDENTIAL PRIMARY MATCHING FUND DEFINITIONS § 9032.11 State. State means each State of the United States, Puerto Rico,...

  17. 11 CFR 9032.11 - State.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 11 Federal Elections 1 2010-01-01 2010-01-01 false State. 9032.11 Section 9032.11 Federal Elections FEDERAL ELECTION COMMISSION PRESIDENTIAL ELECTION CAMPAIGN FUND: PRESIDENTIAL PRIMARY MATCHING FUND DEFINITIONS § 9032.11 State. State means each State of the United States, Puerto Rico,...

  18. Understanding the function and performance of carbon-enhanced lead-acid batteries : milestone report for the DOE Energy Storage Systems program (FY11 Quarter 2: January through March 2011).

    SciTech Connect

    Shane, R.; Enos, David George; Hund, Thomas D.

    2011-05-01

    This report describes the status of research being performed under CRADA No. SC10/01771.00 (Lead/Carbon Functionality in VRLA Batteries) between Sandia National Laboratories and East Penn Manufacturing, conducted for the U.S. Department of Energy's Energy Storage Systems Program. The Quarter 2 Milestone was completed on time. The milestone entails an ex situ analysis of the four carbons that have been added to the negative active material of valve-regulated lead-acid (VRLA) batteries for the purposes of this study. The four carbons selected for this study were a graphitic carbon, a carbon black, an activated carbon, and acetylene black. The morphology, crystallinity, and impurity contents of each of the four carbons were analyzed; results were consistent with previous data. Cycling on a subset of the received East Penn cells containing different carbons (and a control) has been initiated. Carbon has been explored as an addition to lead-acid battery electrodes in a number of ways. Perhaps the most notable to date has been the hybrid 'Ultrabattery' developed by CSIRO where an asymmetric carbon-based electrochemical capacitor is combined with a lead-acid battery into a single cell, dramatically improving high-rate partial-state-of-charge (HRPSoC) operation. As illustrated below, the 'Ultrabattery' is a hybrid device constructed using a traditional lead-acid battery positive plate (i.e., PbO{sub 2}) and a negative electrode consisting of a carbon electrode in parallel with a lead-acid negative plate. This device exhibits a dramatically improved cycle life over traditional VRLA batteries, as well as increased charge power and charge acceptance. The 'Ultrabattery' has been produced successfully by both The Furukawa Battery Co. and East Penn Manufacturing. An example illustrating the dramatic improvement in cycle life of the Ultrabattery over a conventional VRLA battery is shown.

  19. 11CO2 fixation: a renaissance in PET radiochemistry.

    PubMed

    Rotstein, Benjamin H; Liang, Steven H; Holland, Jason P; Collier, Thomas Lee; Hooker, Jacob M; Wilson, Alan A; Vasdev, Neil

    2013-06-25

    Carbon-11 labelled carbon dioxide is the cyclotron-generated feedstock reagent for most positron emission tomography (PET) tracers using this radionuclide. Most carbon-11 labels, however, are installed using derivative reagents generated from [(11)C]CO2. In recent years, [(11)C]CO2 has seen a revival in applications for the direct incorporation of carbon-11 into functional groups such as ureas, carbamates, oxazolidinones, carboxylic acids, esters, and amides. This review summarizes classical [(11)C]CO2 fixation strategies using organometallic reagents and then focuses on newly developed methods that employ strong organic bases to reversibly capture [(11)C]CO2 into solution, thereby enabling highly functionalized labelled compounds to be prepared. Labelled compounds and radiopharmaceuticals that have been translated to the clinic are highlighted.

  20. Understanding the function and performance of carbon-enhanced lead-acid batteries : milestone report for the DOE Energy Storage Systems program (FY11 Quarter 1: October through December 2010).

    SciTech Connect

    Shane, R.; Enos, David George; Hund, Thomas D.

    2011-05-01

    This report describes the status of research being performed under CRADA No. SC10/01771.00 (Lead/Carbon Functionality in VRLA Batteries) between Sandia National Laboratories and East Penn Manufacturing, conducted for the U.S. Department of Energy's Energy Storage Systems Program. The Quarter 1 Milestone was completed on time. The milestone entails conducting a thorough literature review to establish the current level of understanding of the mechanisms through which carbon additions to the negative active material improve valve-regulated lead-acid (VRLA) batteries. Most studies have entailed phenomenological research observing that the carbon additions prevent/reduce sulfation of the negative electrode; however, no understanding is available to provide insight into why certain carbons are successful while others are not. Impurities were implicated in one recent review of the electrochemical behavior of carbon additions. Four carbon samples have been received from East Penn Manufacturing and impurity contents have been analyzed. Carbon has been explored as an addition to lead-acid battery electrodes in a number of ways. Perhaps the most notable to date has been the hybrid 'Ultrabattery' developed by CSIRO where an asymmetric carbon-based electrochemical capacitor is combined with a lead-acid battery into a single cell, dramatically improving high-rate partial-state-of-charge (HRPSoC) operation. As illustrated below, the 'Ultrabattery' is a hybrid device constructed using a traditional lead-acid battery positive plate (i.e., PbO{sub 2}) and a negative electrode consisting of a carbon electrode in parallel with a lead-acid negative plate. This device exhibits a dramatically improved cycle life over traditional VRLA batteries, as well as increased charge power and charge acceptance. The 'Ultrabattery' has been produced successfully by both The Furukawa Battery Co. and East Penn Manufacturing. An example illustrating the dramatic improvement in cycle life of the

  1. Carbon Pneumoconiosis

    PubMed Central

    Miller, A. A.; Ramsden, F.

    1961-01-01

    The occurrence of carbon pneumoconiosis in rubber-factory workers is unusual: the case reported here was discovered in a routine post-mortem examination. The report includes the clinical, radiological, morbid anatomical, and histological findings on a man who had worked in the carbon black store of a rubber works for a continuous period of 21 years, followed by 11 years in the calender department of the same factory. At the age of 65 years the man was retired on the grounds of age and indifferent health: he collapsed and died soon afterwards. The medical history of severe cough with expectoration suggested that he may have had pulmonary tuberculosis in earlier life and some supporting evidence of this infection was found in that his wife contracted this disease after marriage and subsequently died from tuberculosis. The appearances of massive fibrosis in the upper lobes of the lungs suggested that the combined action of carbon black and tuberculosis had produced an “infective” type of pneumoconiosis: in the lower lobes there was far less fibrosis and the appearances were those of simple pneumoconiosis. In addition to the fibrosis the lungs showed nodules of black dust with severe perifocal emphysema. Electron microscopy of the lung dust showed two distinct components and they were similar to samples of channel and thermal blacks which were the main types of carbon used in the factory. This case is an example of pneumoconiosis due to virtually non-siliceous carbon and illustrates that prolonged exposure to heavy dust concentration produces such lesions as described in this paper. Images PMID:13770721

  2. Understanding the function and performance of carbon-enhanced lead-acid batteries : milestone report for the DOE energy storage systems program (FY11 Quarter 3: April through June 2011).

    SciTech Connect

    Ferreira, Summer Rhodes; Shane, Rodney; Enos, David George

    2011-09-01

    This report describes the status of research being performed under CRADA No. SC10/01771.00 (Lead/Carbon Functionality in VRLA Batteries) between Sandia National Laboratories and East Penn Manufacturing, conducted for the U.S. Department of Energy's Energy Storage Systems Program. The Quarter 3 Milestone was completed on time. The milestone entails an ex situ analysis of a control as well as three carbon-containing negative plates in the raw, as cast form as well as after formation. The morphology, porosity, and porosity distribution within each plate was evaluated. In addition, baseline electrochemical measurements were performed on each battery to establish their initial performance. These measurements included capacity, internal resistance, and float current. The results obtained for the electrochemical testing were in agreement with previous evaluations performed at East Penn manufacturing. Cycling on a subset of the received East Penn cells containing different carbons (and a control) has been initiated.

  3. Synthesis, crystal structure, and explosive decomposition of 1,2:5,6: 11,12:15,16-tetrabenzo-3,7,9,13,17,19-hexadehydro[20] annulene: formation of onion- and tube-like closed-shell carbon particles

    SciTech Connect

    Boese, R.; Matzger, A.J.; Vollhardt, K.P.C. |

    1997-02-26

    We have reported that tribenzotetradehydro[14]annulene 1 undergoes topochemical polymerization that results in a novel polyannulenoenyne. In this connection, the `expanded` title compound 2a suggested itself as a promising candidate on route to unprecedented annulene-crosslinked polyenynes. We report the very different physical and chemical behavior of 2a, most importantly its explosive transformation to methane, hydrogen, and extensively ordered pure carbon. Present results give a clear validation of the notion that dehydroannulenes might be potential precursors to carbon allotropes. 28 refs., 1 fig.

  4. Understanding the function and performance of carbon-enhanced lead-acid batteries : milestone report for the DOE Energy Storage Systems Program (FY11 Quarter 4: July through September 2011).

    SciTech Connect

    Ferreira, Summer Rhodes; Shane, Rodney; Enos, David George

    2011-10-01

    This report describes the status of research being performed under CRADA No. SC10/01771.00 (Lead/Carbon Functionality in VRLA Batteries) between Sandia National Laboratories and East Penn Manufacturing, conducted for the U.S. Department of Energy's Energy Storage Systems Program. The Quarter 4 Milestone was completed on time. The milestone entails the initiation of high rate, partial state of charge (HRPSoC) cycling of the carbon enhanced batteries. The morphology, porosity, and porosity distribution within the plates after 1k and 10k cycles were documented, illustrating the changes which take place in the early life of the carbon containing batteries, and as the battery approaches failure due to hard sulfation for the control battery. Longer term cycling on a subset of the received East Penn cells containing different carbons (and a control) continues, and will progress into FY12. Carbon has been explored as an addition to lead-acid battery electrodes in a number of ways. Perhaps the most notable to date has been the hybrid 'Ultrabattery' developed by CSIRO where an asymmetric carbon-based electrochemical capacitor is combined with a lead-acid battery into a single cell, dramatically improving high-rate partial-state-of-charge (HRPSoC) operation. As illustrated below, the 'Ultrabattery' is a hybrid device constructed using a traditional lead-acid battery positive plate (i.e., PbO2) and a negative electrode consisting of a carbon electrode in parallel with a lead-acid negative plate. This device exhibits a dramatically improved cycle life over traditional VRLA batteries, as well as increased charge power and charge acceptance. The 'Ultrabattery' has been produced successfully by both The Furukawa Battery Co. and East Penn Manufacturing. An example illustrating the dramatic improvement in cycle life of the Ultrabattery over a conventional VRLA battery is shown in a graph. In addition to the aforementioned hybrid device, carbon has also been added directly to

  5. The series of carbon-chain complexes {Ru(dppe)Cp*}₂{μ-(C≡C)x} (x = 4–8, 11): Synthesis, structures, properties and some reactions

    SciTech Connect

    Bruce, Michael I.; Cole, Marcus L.; Ellis, Benjamin G.; Gaudio, Maryka; Nicholson, Brian K.; Parker, Christian R.; Skelton, Brian W.; White, Allan H.

    2015-01-28

    The construction of a series of compounds {Ru(dppe)Cp*}2(μ-C2x) (Ru*-C2x-Ru*, x = 4–8, 11)) is described. A direct reaction between RuCl(dppe)Cp* and Me3Si(Ctriple bond; length of mdashC)4SiMe3 afforded Ru*-C8-Ru* in 89% yield. The Pd(0)/Cu(I)-catalysed coupling of Ru{Ctriple bond; length of mdashCCtriple bond; length of mdashCAu(PPh3)}(dppe)Cp*Ru*-C4-Au (2 equiv.) with diiodoethyne gave Ru*-C10-Ru* (64%), or of 1 equiv. with I(Ctriple bond; length of mdashC)3I gave Ru*-C14-Ru* (36%); similarly, Ru{(Ctriple bond; length of mdashC)4Au(PPh3)}(dppe)Cp*Ru*-C8-Au and I(Ctriple bond; length of mdashC)3I gave Ru*-C22-Ru* (12%). Desilylation (TBAF) of Ru{(Ctriple bond; length of mdashC)xSiMe3}(dppe)Cp*Ru*-C2x-Si (x = 3, 4) followed by oxidative coupling [Cu(OAc)2/py] gave Ru*-C12-Ru* (82%) and Ru*-C16-Ru* (58%), respectively. Similar oxidative coupling of Ru(Ctriple bond; length of mdashCCtriple bond; length of mdashCH)(dppe)Cp* was a second route to Ru*-C8-Ru* (82%). Appropriate precursors are already known, or obtained by coupling of Ru*-C2x-Si (x = 2, 4) with AuCl(PPh3)/NaOMe [Ru*-C4-Au, 95%; Ru*-C8-Au, 74%] or from Pd(0)/Cu(I) catalysed coupling of Ru*-C2x-Au (x = 2, 3) with I(Ctriple bond; length of mdashC)2SiMe3 (Ru*-C8-Si, 64%; Ru*-C10-Si, 2%). Reactions between Ru*-C2x-Ru* (x = 3, 4) and Fe2(CO)9 gave {Fe3(CO)9}{μ3-CCtriple bond; length of mdashC[Ru(dppe)Cp*]}2Fe(C3-Ru*)2 and {Fe3(CO)9}{μ3-CCtriple bond; length of mdashC[Ru(dppe)Cp*]}{μ3-C(Ctriple bond; length of mdashC)2[Ru(dppe)Cp*]} Fe(C3-Ru*)(C5-Ru*), respectively. The redox properties of the series of complexes with 2x = 2–16 were measured and showed a diminution of the

  6. Evaluation of carbon-11-labeled 2beta-carbomethoxy-3beta-[4'-((Z)-2-iodoethenyl)phenyl]nortropane as a potential radioligand for imaging the serotonin transporter by PET.

    PubMed

    Plisson, Christophe; Jarkas, Nachwa; McConathy, Jon; Voll, Ronald J; Votaw, John; Williams, Larry; Howell, Leonard L; Kilts, Clinton D; Goodman, Mark M

    2006-02-01

    The nortropane cocaine analogue, 2beta-carbomethoxy-3beta-[4'-((Z)-2-iodoethenyl)phenyl]nortropane (ZIENT), is a high affinity, selective serotonin transporter (SERT) ligand that has shown promise as a SERT imaging agent for single photon computed tomography (SPECT) when labeled with I-123. Synthesis of the labeling precursor, radiosynthesis of [(11)C]ZIENT, and in vivo evaluation in anesthetized and awake monkeys have been performed to determine the suitability of [(11)C]ZIENT as a PET agent for SERT imaging. PMID:16451060

  7. Carbon isotope techniques

    SciTech Connect

    Coleman, D.C. ); Fry, B. )

    1991-01-01

    This book is a hands-on introduction to using carbon isotope tracers in experimental biology and ecology. It is a bench-top reference with protocols for the study of plants, animals, and soils. The {sup 11}C, {sup 12}C, {sup 13}C, and {sup 14}C carbon isotopes are considered and standard techniques are described by established authors. The compilation includes the following features: specific, well-established, user-oriented techniques; carbon cycles in plants, animals, soils, air, and water; isotopes in ecological research; examples and sample calculations.

  8. Supplies tight for CFC-11 and -12

    SciTech Connect

    Rotman, D.; Kirschner, E.

    1992-09-30

    With US 1992 production of chlorofluorocarbon (CFC)-11 and -12 cut back to less than 50% of 1986 levels, supplies are tight and prices are rising. While CFC customers can find the product, the first half of the year was particularly bumpy, marked by shortages of key feedstock carbon tetrachloride. US carbon tet production dropped from 400 million lbs in 1991 to 250 million lbs because of a series of plant closings in 1991. The lack of carbon tet, says a spokesman for one CFC producer, was [open quotes]a real disruption.[close quotes] And, says Jerry Dziedzic, general manager, fluorochemicals at Elf Atochem (Philadelphia), in a such a tight market [open quotes]even a little hiccup can throw the system out of whack.[close quotes] Dow senior project manager Jeff Sullivan says CFC producers were expecting a drop in 1992 sales when the company's Sarnia, ON carbon tet plant closing was announced. By the time CFC producers recognized that demand would remain at 1991 levels, the shutdown was under way. [open quotes]We were caught short because they were caught short.[close quotes] While the carbon tet shortage has lessened recently, supplies of CFC-11 and 12 are expected to remain tight through the rest of the year. But that could ease toward year-end as hydrofluorocarbon-141b increasingly replaces CFC-11.

  9. Complexes with biologically active ligands. Part 11. Synthesis and carbonic anhydrase inhibitory activity of metal complexes of 4,5-disubstituted-3-mercapto-1,2,4-triazole derivatives.

    PubMed

    Scozzafava, A; Cavazza, C; Supuran, C T; Saramet, I; Briganti, F; Banciu, M D

    1998-01-01

    Complexes containing five 4,5-disubstituted-3-mercapto-1,2,4-triazoles and Zn(II), Hg(II) and Cu(I) were synthesized and characterized by standard procedures (elemental analysis; IR, electronic and NMR spectroscopy, conductimetry and TG analysis). Both the thione as well as the thiolate forms of the ligands were evidenced to interact with the metal ions in the prepared complexes. The original mercaptans and their metal complexes behave as inhibitors of three carbonic anhydrase (CA) isozymes, CA I, II and IV, but did not lower intraocular pressure in rabbits in animal models of glaucoma.

  10. Infrared laser absorption spectroscopy of the nu4 (sigma u) fundamental and associated nu11(pi u) hot band of C7 - Evidence for alternating rigidity in linear carbon clusters

    NASA Technical Reports Server (NTRS)

    Heath, J. R.; Saykally, R. J.

    1991-01-01

    The first characterization of the bending potential of the C7 cluster is reported via the observation of the v = 1(1) and v = 2 deg levels of the nu11 (pi u) bend as hot bands associated with the nu4 (sigma u) antisymmetric stretch fundamental. The lower state hot band rotational constants are measured to be 1004.4(1.3) and 1123.6(9.0) MHz, constituting a 9.3 and 22 percent increase over the ground state rotational constant, 918.89 (41) MHz. These large increases are strong quartic and sextic centrifugal distortion constants determined for the ground and nu 4 = 1 states are found to be anomalously large and negative, evidencing strong perturbations between stretching and bending modes.

  11. 11. POWERHOUSE INTERIOR, DETAIL OF EXCITER No. 2 GENERAL ELECTRIC ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    11. POWERHOUSE INTERIOR, DETAIL OF EXCITER No. 2 GENERAL ELECTRIC GENERATOR SHOWING COPPER COMMUTATOR AND CARBON BRUSHES. VIEW TO NORTHEAST. - Rush Creek Hydroelectric System, Powerhouse Exciters, Rush Creek, June Lake, Mono County, CA

  12. 40 CFR 86.201-11 - General applicability.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...-Duty Passenger Vehicles; Cold Temperature Test Procedures § 86.201-11 General applicability. (a) This subpart describes procedures for determining the cold temperature carbon monoxide (CO) emissions from...

  13. 40 CFR 86.201-11 - General applicability.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...-Duty Passenger Vehicles; Cold Temperature Test Procedures § 86.201-11 General applicability. (a) This subpart describes procedures for determining the cold temperature carbon monoxide (CO) emissions from...

  14. Carbon-carbon cylinder block

    NASA Technical Reports Server (NTRS)

    Ransone, Philip O. (Inventor)

    1998-01-01

    A lightweight cylinder block composed of carbon-carbon is disclosed. The use of carbon-carbon over conventional materials, such as cast iron or aluminum, reduces the weight of the cylinder block and improves thermal efficiency of the internal combustion reciprocating engine. Due to the negligible coefficient of thermal expansion and unique strength at elevated temperatures of carbon-carbon, the piston-to-cylinder wall clearance can be small, especially when the carbon-carbon cylinder block is used in conjunction with a carbon-carbon piston. Use of the carbon-carbon cylinder block has the effect of reducing the weight of other reciprocating engine components allowing the piston to run at higher speeds and improving specific engine performance.

  15. Carbon Smackdown: Carbon Capture

    ScienceCinema

    Jeffrey Long

    2016-07-12

    In this July 9, 2010 Berkeley Lab summer lecture, Lab scientists Jeff Long of the Materials Sciences and Nancy Brown of the Environmental Energy Technologies Division discuss their efforts to fight climate change by capturing carbon from the flue gas of power plants, as well as directly from the air

  16. Carbon Smackdown: Carbon Capture

    SciTech Connect

    Jeffrey Long

    2010-07-12

    In this July 9, 2010 Berkeley Lab summer lecture, Lab scientists Jeff Long of the Materials Sciences and Nancy Brown of the Environmental Energy Technologies Division discuss their efforts to fight climate change by capturing carbon from the flue gas of power plants, as well as directly from the air

  17. The 11 Micron Emissions of Cabon Stars

    NASA Technical Reports Server (NTRS)

    Goebel, J. H.; Cheeseman, P.; Gerbault, F.

    1995-01-01

    A new classification scheme of the IRAS LRS carbon stars is presented. It comprises the separation of 718 probable carbon stars into 12 distinct self-similar spectral groupings. Continuum temperatures are assigned and range from 470 to 5000 K. Three distinct dust species are identifiable: SiC, alpha:C-H, and MgS. In addition to the narrow 11 + micron emission feature that is commonly attributed to SiC, a broad 11 + micron emission feature, that is correlated with the 8.5 and 7.7 micron features, is found and attributed to alpha:C-H. SiC and alpha:C-H band strengths are found to correlate with the temperature progression among the Classes. We find a spectral sequence of Classes that reflects the carbon star evolutionary sequence of spectral types, or alternatively developmental sequences of grain condensation in carbon-rich circumstellar shells. If decreasing temperature corresponds to increasing evolution, then decreasing temperature corresponds to increasing CIO resulting in increasing amounts of carbon rich dust, namely alpha:C-H. If decreasing the temperature corresponds to a grain condensation sequence, then heterogeneous, or induced nucleation scenarios are supported. SiC grains precede alpha:C-H and form the nuclei for the condensation of the latter material. At still lower temperatures, MgS appears to be quite prevalent. No 11.3 micron PAH features are identified in any of the 718 carbon stars. However, one of the coldest objects, IRAS 15048-5702, and a few others, displays an 11.9 micron emission feature characteristic of laboratory samples of coronene. That feature corresponds to the C-H out of plane deformation mode of aromatic hydrocarbon. This band indicates the presence of unsaturated, sp(sup 3), hydrocarbon bonds that may subsequently evolve into saturated bonds, sp(sup 2), if, and when, the star enters the planetary nebulae phase of stellar evolution. The effusion of hydrogen from the hydrocarbon grain results in the evolution in wavelength of this

  18. Carbon-carbon piston development

    NASA Technical Reports Server (NTRS)

    Gorton, Mark P.

    1994-01-01

    A new piston concept, made of carbon-carbon refractory-composite material, has been developed that overcomes a number of the shortcomings of aluminum pistons. Carbon-carbon material, developed in the early 1960's, is lighter in weight than aluminum, has higher strength and stiffness than aluminum and maintains these properties at temperatures over 2500 F. In addition, carbon-carbon material has a low coefficient of thermal expansion and excellent resistance to thermal shock. An effort, called the Advanced Carbon-Carbon Piston Program was started in 1986 to develop and test carbon-carbon pistons for use in spark ignition engines. The carbon-carbon pistons were designed to be replacements for existing aluminum pistons, using standard piston pin assemblies and using standard rings. Carbon-carbon pistons can potentially enable engines to be more reliable, more efficient and have greater power output. By utilizing the unique characteristics of carbon-carbon material a piston can: (1) have greater resistance to structural damage caused by overheating, lean air-fuel mixture conditions and detonation; (2) be designed to be lighter than an aluminum piston thus, reducing the reciprocating mass of an engine, and (3) be operated in a higher combustion temperature environment without failure.

  19. Apollo 11 Launch

    NASA Technical Reports Server (NTRS)

    1994-01-01

    On 16 July 1969, American astronauts Neil Armstrong, Edwin 'Buzz' Aldrin, and Michael Collins lifted off from Cape Canaveral, Fla., in the mammoth-sized Saturn V rocket on their way to the moon during the Apollo 11 mission. Cmdr. Armstrong and pilot Aldrin landed the spacecraft, Eagle, on the moon's Sea of Tranquillity. Apollo 11 booster stages were tested at Stennis Space Center.

  20. Carbon and its isotopes in mid-oceanic basaltic glasses

    NASA Technical Reports Server (NTRS)

    Des Marais, D. J.; Moore, J. G.

    1984-01-01

    Sample surface carbon, mantle carbon dioxide in vesicles, and mantle carbon dissolved in glasses, are the three carbon components evident in the 11 mid-oceanic basalts presently analyzed. The total carbon content may be controlled by the depth of the shallowest ridge magma chamber, and carbon isotopic fractionation accompanies magma degassing. Using He-3 and carbon data for submarine hydrothermal fluids, the present day midoceanic ridge carbon flux is approximately estimated to be 1.0 x 10 to the 13th g C/yr, requiring 8 Gyr to accumulate the earth's present crustal carbon inventory.

  1. High pressure study of low compressibility tetracalcium aluminum carbonate hydrates 3CaO{center_dot}Al{sub 2}O{sub 3}{center_dot}CaCO{sub 3}{center_dot}11H{sub 2}O

    SciTech Connect

    Moon, Juhyuk; Oh, Jae Eun; Balonis, Magdalena; Glasser, Fredrik P.; Clark, Simon M.; Monteiro, Paulo J.M.

    2012-01-15

    Synchrotron X-ray diffraction data was collected from a sample of monocarboaluminate 3CaO{center_dot}Al{sub 2}O{sub 3}{center_dot}CaCO{sub 3}{center_dot}11H{sub 2}O from ambient pressure to 4.3 GPa. The refined crystal structure at ambient pressure is triclinic with parameters a = 5.77(2) A, b = 8.47(5) A, c = 9.93(4) A, {alpha} = 64.6(2) Degree-Sign , {beta} = 82.8(3) Degree-Sign , {gamma} = 81.4(4) Degree-Sign , and space group of P1 or P1{sup Macron }. It showed some degree of perfectly reversible pressure-induced dehydration with a non-hygroscopic pressure-transmitting medium. However the dehydration effect does not critically affect a bulk modulus due to its strong framework. The isothermal bulk modulus of monocarboaluminate was found to be 53(5) GPa and 54(4) GPa with 3rd order and 2nd order Birch-Murnaghan Equation of state, respectively. That value is higher than for any other reported AFm or AFt phase. The pressure-volume behavior of the monocarboaluminate was compared with that of previous studied hemicarboaluminate.

  2. Apollo 11 lunar photography

    NASA Technical Reports Server (NTRS)

    Anderson, A. T.; Michlovitz, C. K.; Hug, K.

    1970-01-01

    A data user's note is presented which announces the availability of the complete set of Apollo 11 pictorial data and aids investigators in the selection of Apollo 11 photographs for study. In addition, this note provides guidance in the interpretation of the photographs. As background information, brief descriptions of the Apollo 11 mission objectives, photographic equipment, and photographic coverage and quality are included. The National Space Science Data Center (NSSDC) can provide all forms of photographs described in the section on format of available data.

  3. Calcium Carbonate

    MedlinePlus

    Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not ... for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve ...

  4. Carbon photonics

    NASA Astrophysics Data System (ADS)

    Konov, V. I.

    2015-11-01

    The properties of new carbon materials (single-crystal and polycrystalline CVD diamond films and wafers, single-wall carbon nanotubes and graphene) and the prospects of their use as optical elements and devices are discussed.

  5. 46 CFR 11.103-11.105 - [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 1 2010-10-01 2010-10-01 false 11.103-11.105 Section 11.103-11.105 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY MERCHANT MARINE OFFICERS AND SEAMEN REQUIREMENTS FOR OFFICER ENDORSEMENTS General §§ 11.103-11.105...

  6. 46 CFR 11.109-11.113 - [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 1 2010-10-01 2010-10-01 false 11.109-11.113 Section 11.109-11.113 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY MERCHANT MARINE OFFICERS AND SEAMEN REQUIREMENTS FOR OFFICER ENDORSEMENTS General §§ 11.109-11.113...

  7. Morpheus Tether Test #11

    NASA Video Gallery

    Morpheus conducts another tethered test, April 11, 2012. Morpheus is a full spacecraft and rocket-powered lander, which demonstrates new green technology, as well as an autonomous landing and hazar...

  8. September 11, 2001.

    ERIC Educational Resources Information Center

    Wilkinson, Christine K.

    2002-01-01

    The September 11 terrorist attacks in the United States had an impact on everyone across the nation, and certainly included college campuses. This article addresses campus responses targeted at students and identifies future implications. (Contains 20 references.) (Author)

  9. The Toxicology of Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Donaldson, Ken; Poland, Craig; Duffin, Rodger; Bonner, James

    2012-06-01

    1. Carbon nanotube structure, synthesis and applications C. Singh and W. Song; 2. The aerodynamic behaviour and pulmonary deposition of carbon nanotubes A. Buckley, R. Smith and R Maynard; 3. Utilising the concept of the biologically effective dose to define the particle and fibre hazards of carbon nanotubes K. Donaldson, R. Duffin, F. Murphy and C. Poland; 4. CNT, biopersistence and the fibre paradigm D. Warheit and M. DeLorme; 5. Length-dependent retention of fibres in the pleural space C. Poland, F. Murphy and K. Donaldson; 6. Experimental carcinogenicity of carbon nanotubes in the context of other fibres K. Unfried; 7. Fate and effects of carbon nanotubes following inhalation J. Ryman-Rasmussen, M. Andersen and J. Bonner; 8. Responses to pulmonary exposure to carbon nanotubes V. Castranova and R. Mercer; 9. Genotoxicity of carbon nanotubes R. Schins, C. Albrecht, K. Gerloff and D. van Berlo; 10. Carbon nanotube-cellular interactions; macrophages, epithelial and mesothelial cells V. Stone, M. Boyles, A. Kermanizadeh, J. Varet and H. Johnston; 11. Systemic health effects of carbon nanotubes following inhalation J. McDonald; 12. Dosimetry and metrology of carbon nanotubes L. Tran, L. MacCalman and R. Aitken; Index.

  10. Palaeoclimatology: the record for marine isotopic stage 11.

    PubMed

    Raynaud, Dominique; Barnola, Jean-Marc; Souchez, Roland; Lorrain, Reginald; Petit, Jean-Robert; Duval, Paul; Lipenkov, Vladimir Y

    2005-07-01

    The marine isotopic stage 11 (MIS 11) is an extraordinarily long interglacial period in the Earth's history that occurred some 400,000 years ago and lasted for about 30,000 years. During this period there were weak, astronomically induced changes in the distribution of solar energy reaching the Earth. The conditions of this orbital climate forcing are similar to those of today's interglacial period, and they rendered the climate susceptible to other forcing--for example, to changes in the level of atmospheric carbon dioxide. Here we use ice-core data from the Antarctic Vostok core to reconstruct a complete atmospheric carbon dioxide record for MIS 11. The record indicates that values for carbon dioxide throughout the interglacial period were close to the Earth's pre-industrial levels and that both solar energy and carbon dioxide may have helped to make MIS 11 exceptionally long. Anomalies in the oceanic carbonate system recorded in marine sediments at the time, for example while coral reefs were forming, apparently left no signature on atmospheric carbon dioxide concentrations.

  11. 11 CFR 9034.11 - Winding down costs.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... shall not exceed the lesser of: (1) 10% of the overall expenditure limitation pursuant to 11 CFR 9035.1... 11 Federal Elections 1 2010-01-01 2010-01-01 false Winding down costs. 9034.11 Section 9034.11... MATCHING FUND ENTITLEMENTS § 9034.11 Winding down costs. (a) Winding down costs. Winding down costs...

  12. 11 CFR 9004.11 - Winding down costs.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... expenditure limitation pursuant to 11 CFR 110.8(a)(2); or (2) 2.5% of the total of: (i) The candidate's... 11 Federal Elections 1 2010-01-01 2010-01-01 false Winding down costs. 9004.11 Section 9004.11... FINANCING ENTITLEMENT OF ELIGIBLE CANDIDATES TO PAYMENTS; USE OF PAYMENTS § 9004.11 Winding down costs....

  13. 11 CFR 9034.11 - Winding down costs.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... shall not exceed the lesser of: (1) 10% of the overall expenditure limitation pursuant to 11 CFR 9035.1... 11 Federal Elections 1 2013-01-01 2012-01-01 true Winding down costs. 9034.11 Section 9034.11... MATCHING FUND ENTITLEMENTS § 9034.11 Winding down costs. (a) Winding down costs. Winding down costs...

  14. 11 CFR 9004.11 - Winding down costs.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... expenditure limitation pursuant to 11 CFR 110.8(a)(2); or (2) 2.5% of the total of: (i) The candidate's... 11 Federal Elections 1 2012-01-01 2012-01-01 false Winding down costs. 9004.11 Section 9004.11... FINANCING ENTITLEMENT OF ELIGIBLE CANDIDATES TO PAYMENTS; USE OF PAYMENTS § 9004.11 Winding down costs....

  15. 11 CFR 9034.11 - Winding down costs.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... shall not exceed the lesser of: (1) 10% of the overall expenditure limitation pursuant to 11 CFR 9035.1... 11 Federal Elections 1 2011-01-01 2011-01-01 false Winding down costs. 9034.11 Section 9034.11... MATCHING FUND ENTITLEMENTS § 9034.11 Winding down costs. (a) Winding down costs. Winding down costs...

  16. 11 CFR 9004.11 - Winding down costs.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... expenditure limitation pursuant to 11 CFR 110.8(a)(2); or (2) 2.5% of the total of: (i) The candidate's... 11 Federal Elections 1 2011-01-01 2011-01-01 false Winding down costs. 9004.11 Section 9004.11... FINANCING ENTITLEMENT OF ELIGIBLE CANDIDATES TO PAYMENTS; USE OF PAYMENTS § 9004.11 Winding down costs....

  17. 11 CFR 9034.11 - Winding down costs.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... shall not exceed the lesser of: (1) 10% of the overall expenditure limitation pursuant to 11 CFR 9035.1... 11 Federal Elections 1 2014-01-01 2014-01-01 false Winding down costs. 9034.11 Section 9034.11... MATCHING FUND ENTITLEMENTS § 9034.11 Winding down costs. (a) Winding down costs. Winding down costs...

  18. 11 CFR 9004.11 - Winding down costs.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... expenditure limitation pursuant to 11 CFR 110.8(a)(2); or (2) 2.5% of the total of: (i) The candidate's... 11 Federal Elections 1 2013-01-01 2012-01-01 true Winding down costs. 9004.11 Section 9004.11... FINANCING ENTITLEMENT OF ELIGIBLE CANDIDATES TO PAYMENTS; USE OF PAYMENTS § 9004.11 Winding down costs....

  19. 11 CFR 9034.11 - Winding down costs.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... shall not exceed the lesser of: (1) 10% of the overall expenditure limitation pursuant to 11 CFR 9035.1... 11 Federal Elections 1 2012-01-01 2012-01-01 false Winding down costs. 9034.11 Section 9034.11... MATCHING FUND ENTITLEMENTS § 9034.11 Winding down costs. (a) Winding down costs. Winding down costs...

  20. 11 CFR 9004.11 - Winding down costs.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... expenditure limitation pursuant to 11 CFR 110.8(a)(2); or (2) 2.5% of the total of: (i) The candidate's... 11 Federal Elections 1 2014-01-01 2014-01-01 false Winding down costs. 9004.11 Section 9004.11... FINANCING ENTITLEMENT OF ELIGIBLE CANDIDATES TO PAYMENTS; USE OF PAYMENTS § 9004.11 Winding down costs....

  1. Carbon-Carbon Piston Architectures

    NASA Technical Reports Server (NTRS)

    Rivers, H. Kevin (Inventor); Ransone, Philip O. (Inventor); Northam, G. Burton (Inventor); Schwind, Francis A. (Inventor)

    1999-01-01

    An improved structure for carbon-carbon composite piston architectures consists of replacing the knitted fiber, three-dimensional piston preform architecture described in U.S. Pat. No. 4.909,133 (Taylor et al.) with a two-dimensional lay-up or molding of carbon fiber fabric or tape. Initially. the carbon fabric or tape layers are prepregged with carbonaceous organic resins and/or pitches and are laid up or molded about a mandrel. to form a carbon-fiber reinforced organic-matrix composite part shaped like a "U" channel, a "T"-bar. or a combination of the two. The molded carbon-fiber reinforced organic-matrix composite part is then pyrolized in an inert atmosphere, to convert the organic matrix materials to carbon. At this point, cylindrical piston blanks are cored from the "U" channel, "T"-bar, or combination part. These blanks are then densified by reimpregnation with resins or pitches which are subsequently carbonized. Densification is also be accomplished by direct infiltration with carbon by vapor deposition processes. Once the desired density has been achieved, the piston billets are machined to final piston dimensions; coated with oxidation sealants; and/or coated with a catalyst. When compared to conventional steel or aluminum-alloy pistons, the use of carbon-carbon composite pistons reduces the overall weight of the engine; allows for operation at higher temperatures without a loss of strength; allows for quieter operation; reduces the heat loss; and reduces the level of hydrocarbon emissions.

  2. 1,1-Difluoroethane

    Integrated Risk Information System (IRIS)

    1,1 - Difluoroethane ; CASRN 75 - 37 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogen

  3. 1,1-Dichloroethane

    Integrated Risk Information System (IRIS)

    1,1 - Dichloroethane ; CASRN 75 - 34 - 3 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogen

  4. Log of Apollo 11.

    ERIC Educational Resources Information Center

    National Aeronautics and Space Administration, Washington, DC.

    The major events of the first manned moon landing mission, Apollo 11, are presented in chronological order from launch time until arrival of the astronauts aboard the U.S.S. Hornet. The log is descriptive, non-technical, and includes numerous color photographs of the astronauts on the moon. (PR)

  5. Development of carbon-carbon nozzle extension for liquid fuel rocket motors

    NASA Astrophysics Data System (ADS)

    Sokolovsky, M. I.; Petukhov, S. N.; Semyonov, Yu. P.; Sokolov, B. A.

    2008-12-01

    Successful experience of RSC “Energy” and SPA “Iskra” in the development of carbon-carbon extension for oxygen-kerosene liquid fuel rocket motor has been summarized. Methodological approach that served to completion of carbon-carbon extension development in full and at comparatively small expenses has been described. Results of practical application of carbon-carbon extension for liquid fuel rocket motor 11D58M have been presented within the framework of International Space Program “Sea Launch”.

  6. Carbonate aquifers

    USGS Publications Warehouse

    Cunningham, Kevin J.; Sukop, Michael; Curran, H. Allen

    2012-01-01

    Only limited hydrogeological research has been conducted using ichnology in carbonate aquifer characterization. Regardless, important applications of ichnology to carbonate aquifer characterization include its use to distinguish and delineate depositional cycles, correlate mappable biogenically altered surfaces, identify zones of preferential groundwater flow and paleogroundwater flow, and better understand the origin of ichnofabric-related karst features. Three case studies, which include Pleistocene carbonate rocks of the Biscayne aquifer in southern Florida and Cretaceous carbonate strata of the Edwards–Trinity aquifer system in central Texas, demonstrate that (1) there can be a strong relation between ichnofabrics and groundwater flow in carbonate aquifers and (2) ichnology can offer a useful methodology for carbonate aquifer characterization. In these examples, zones of extremely permeable, ichnofabric-related macroporosity are mappable stratiform geobodies and as such can be represented in groundwater flow and transport simulations.

  7. Microstructural Characterization and Mechanical Properties of PA11 Nanocomposite Fibers

    NASA Astrophysics Data System (ADS)

    Latko, Paulina; Kolbuk, Dorota; Kozera, Rafal; Boczkowska, Anna

    2016-01-01

    Polyamide 11/multi-walled carbon nanotubes nanocomposite fibers with weight fraction 2, 4, and 6 wt.% and diameter 80 μm were prepared with a twin screw mini-extruder. The morphology and degree of dispersion of the multi-walled carbon nanotubes in the fibers was investigated by using scanning and transmission electron microscopy. In turn, the molecular structure was indicated by using wide-angle x-ray scattering and correlated with thermal analysis. It was found that carbon nanotubes lead to the formation of α phase in the fibers and they show medial level of alignment within the length of the fiber. Mechanical analysis of the fibers shows that apart from the crystallinity content, the tensile strength is strongly dependent on the macroscopic defects of the surface of the fibers. Nanocomposite fibers based on polyamide 11 with carbon nanotubes can be used as a precursor for non-woven or woven fabrics manufacturing process.

  8. Apollo 11 Crew Portrait

    NASA Technical Reports Server (NTRS)

    1969-01-01

    This is the official crew portrait of the Apollo 11 astronauts. Pictured from left to right are: Neil A. Armstrong, Commander; Michael Collins, Module Pilot; Edwin E. 'Buzz' Aldrin, Lunar Module Pilot. Apollo 11 was the first marned lunar landing mission that placed the first humans on the surface of the moon and returned them back to Earth. Astronaut Armstrong became the first man on the lunar surface, and astronaut Aldrin became the second. Astronaut Collins piloted the Command Module in a parking orbit around the Moon. Launched aboard the Saturn V launch vehicle (SA-506), the three astronauts began their journey to the moon with liftoff from launch complex 39A at the Kennedy Space Center at 8:32 am CDT, July 16, 1969.

  9. Bion 11 mission hardware.

    PubMed

    Golov, V K; Magedov, V S; Skidmore, M G; Hines, J W; Kozlovskaya, I B; Korolkov, V I

    2000-01-01

    The mission hardware provided for Bion 11 shared primate experiments included the launch vehicle, biosatellite, spaceflight operational systems, spacecraft recovery systems, life support systems, bioinstrumentation, and data collection systems. Under the unique Russia/US bilateral contract, the sides worked together to ensure the reliability and quality of hardware supporting the primate experiments. Parameters recorded inflight covered biophysical, biochemical, biopotential, environmental, and system operational status.

  10. Apollo 11 Mission Commemorated

    NASA Astrophysics Data System (ADS)

    Showstack, Randy

    2009-07-01

    On 24 July 1969, 4 days after Apollo 11 Mission Commander Neil Armstrong and Lunar Module Eagle Pilot Eugene “Buzz” Aldrin had become the first people to walk on the Moon, they and Apollo 11 Command Module Pilot Michael Collins peered through a window of the Mobile Quarantine Facility on board the U.S.S. Hornet following splashdown of the command module in the central Pacific as U.S. President Richard Nixon told them, “This is the greatest week in the history of the world since the creation.” Forty years later, the Apollo 11 crew and other Apollo-era astronauts gathered at several events in Washington, D. C., to commemorate and reflect on the Apollo program, that mission, and the future of manned spaceflight. “I don’t know what the greatest week in history is,” Aldrin told Eos. “But it was certainly a pioneering opening the door. With the door open when we touched down on the Moon, that was what enabled humans to put many more footprints on the surface of the Moon.”

  11. 11 CFR 1.1 - Purpose and scope.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 11 Federal Elections 1 2014-01-01 2014-01-01 false Purpose and scope. 1.1 Section 1.1 Federal Elections FEDERAL ELECTION COMMISSION PRIVACY ACT § 1.1 Purpose and scope. (a) The purpose of this part is to set forth rules informing the public as to what information is maintained by the Federal...

  12. 11 CFR 1.1 - Purpose and scope.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 11 Federal Elections 1 2012-01-01 2012-01-01 false Purpose and scope. 1.1 Section 1.1 Federal Elections FEDERAL ELECTION COMMISSION PRIVACY ACT § 1.1 Purpose and scope. (a) The purpose of this part is to set forth rules informing the public as to what information is maintained by the Federal...

  13. 11 CFR 1.1 - Purpose and scope.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 11 Federal Elections 1 2013-01-01 2012-01-01 true Purpose and scope. 1.1 Section 1.1 Federal Elections FEDERAL ELECTION COMMISSION PRIVACY ACT § 1.1 Purpose and scope. (a) The purpose of this part is to set forth rules informing the public as to what information is maintained by the Federal...

  14. 27 CFR 11.11 - Meaning of terms.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2013-04-01 2013-04-01 false Meaning of terms. 11.11... OF THE TREASURY ALCOHOL CONSIGNMENT SALES Definitions § 11.11 Meaning of terms. As used in this part, unless the context otherwise requires, terms have the meanings given in this section. Any other...

  15. 27 CFR 11.11 - Meaning of terms.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2012-04-01 2012-04-01 false Meaning of terms. 11.11... OF THE TREASURY LIQUORS CONSIGNMENT SALES Definitions § 11.11 Meaning of terms. As used in this part, unless the context otherwise requires, terms have the meanings given in this section. Any other...

  16. 27 CFR 11.11 - Meaning of terms.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2014-04-01 2014-04-01 false Meaning of terms. 11.11... OF THE TREASURY ALCOHOL CONSIGNMENT SALES Definitions § 11.11 Meaning of terms. As used in this part, unless the context otherwise requires, terms have the meanings given in this section. Any other...

  17. 11 CFR 9002.11 - Qualified campaign expense.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... committee in accordance with 11 CFR 104.3(h). (c) Except as provided in 11 CFR 9034.4(e), expenditures...'s eligibility will be considered qualified campaign expenses if they meet the provisions of 11 CFR 9004.4(a). Expenditures described under 11 CFR 9004.4(b) will not be considered qualified...

  18. 11 CFR 1.1 - Purpose and scope.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 11 Federal Elections 1 2011-01-01 2011-01-01 false Purpose and scope. 1.1 Section 1.1 Federal Elections FEDERAL ELECTION COMMISSION PRIVACY ACT § 1.1 Purpose and scope. (a) The purpose of this part is to set forth rules informing the public as to what information is maintained by the Federal...

  19. 11 CFR 1.1 - Purpose and scope.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 11 Federal Elections 1 2010-01-01 2010-01-01 false Purpose and scope. 1.1 Section 1.1 Federal Elections FEDERAL ELECTION COMMISSION PRIVACY ACT § 1.1 Purpose and scope. (a) The purpose of this part is to set forth rules informing the public as to what information is maintained by the Federal...

  20. 7 CFR 11.11 - Reconsideration of Director determinations.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 7 Agriculture 1 2012-01-01 2012-01-01 false Reconsideration of Director determinations. 11.11... Appeals Divison Rules of Procedures § 11.11 Reconsideration of Director determinations. (a) Reconsideration of a determination of the Director may be requested by the appellant or the agency within 10...

  1. 7 CFR 11.11 - Reconsideration of Director determinations.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 1 2010-01-01 2010-01-01 false Reconsideration of Director determinations. 11.11... Appeals Divison Rules of Procedures § 11.11 Reconsideration of Director determinations. (a) Reconsideration of a determination of the Director may be requested by the appellant or the agency within 10...

  2. 7 CFR 11.11 - Reconsideration of Director determinations.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 1 2011-01-01 2011-01-01 false Reconsideration of Director determinations. 11.11... Appeals Divison Rules of Procedures § 11.11 Reconsideration of Director determinations. (a) Reconsideration of a determination of the Director may be requested by the appellant or the agency within 10...

  3. 7 CFR 11.11 - Reconsideration of Director determinations.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 7 Agriculture 1 2013-01-01 2013-01-01 false Reconsideration of Director determinations. 11.11... Appeals Divison Rules of Procedures § 11.11 Reconsideration of Director determinations. (a) Reconsideration of a determination of the Director may be requested by the appellant or the agency within 10...

  4. (11)C[double bond, length as m-dash]O bonds made easily for positron emission tomography radiopharmaceuticals.

    PubMed

    Rotstein, Benjamin H; Liang, Steven H; Placzek, Michael S; Hooker, Jacob M; Gee, Antony D; Dollé, Frédéric; Wilson, Alan A; Vasdev, Neil

    2016-08-22

    The positron-emitting radionuclide carbon-11 ((11)C, t1/2 = 20.3 min) possesses the unique potential for radiolabeling of any biological, naturally occurring, or synthetic organic molecule for in vivo positron emission tomography (PET) imaging. Carbon-11 is most often incorporated into small molecules by methylation of alcohol, thiol, amine or carboxylic acid precursors using [(11)C]methyl iodide or [(11)C]methyl triflate (generated from [(11)C]carbon dioxide or [(11)C]methane). Consequently, small molecules that lack an easily substituted (11)C-methyl group are often considered to have non-obvious strategies for radiolabeling and require a more customized approach. [(11)C]Carbon dioxide itself, [(11)C]carbon monoxide, [(11)C]cyanide, and [(11)C]phosgene represent alternative reactants to enable (11)C-carbonylation. Methodologies developed for preparation of (11)C-carbonyl groups have had a tremendous impact on the development of novel PET tracers and provided key tools for clinical research. (11)C-Carbonyl radiopharmaceuticals based on labeled carboxylic acids, amides, carbamates and ureas now account for a substantial number of important imaging agents that have seen translation to higher species and clinical research of previously inaccessible targets, which is a testament to the creativity, utility and practicality of the underlying radiochemistry. PMID:27276357

  5. Carbon-Carbon Piston Architectures

    NASA Technical Reports Server (NTRS)

    Rivers, H. Kevin (Inventor); Ransone, Philip O. (Inventor); Northam, G. Burton (Inventor); Schwind, Francis A. (Inventor)

    2000-01-01

    An improved structure for carbon-carbon composite piston architectures is disclosed. The improvement consists of replacing the knitted fiber, three-dimensional piston preform architecture described in U.S. Pat.No. 4,909,133 (Taylor et al.) with a two-dimensional lay-up or molding of carbon fiber fabric or tape. Initially, the carbon fabric of tape layers are prepregged with carbonaceous organic resins and/or pitches and are laid up or molded about a mandrel, to form a carbon-fiber reinforced organic-matrix composite part shaped like a "U" channel, a "T"-bar, or a combination of the two. The molded carbon-fiber reinforced organic-matrix composite part is then pyrolized in an inert atmosphere, to convert the organic matrix materials to carbon. At this point, cylindrical piston blanks are cored from the "U"-channel, "T"-bar, or combination part. These blanks are then densified by reimpregnation with resins or pitches which are subsequently carbonized. Densification is also accomplished by direct infiltration with carbon by vapor deposition processes. Once the desired density has been achieved, the piston billets are machined to final piston dimensions; coated with oxidation sealants; and/or coated with a catalyst. When compared to conventional steel or aluminum alloy pistons, the use of carbon-carbon composite pistons reduces the overall weight of the engine; allows for operation at higher temperatures without a loss of strength; allows for quieter operation; reduces the heat loss; and reduces the level of hydrocarbon emissions.

  6. 29 CFR 1917.24 - Carbon monoxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... using gas detector tube units certified by NIOSH under 30 CFR part 11 or other measuring instruments... 29 Labor 7 2014-07-01 2014-07-01 false Carbon monoxide. 1917.24 Section 1917.24 Labor Regulations...) MARINE TERMINALS Marine Terminal Operations § 1917.24 Carbon monoxide. (a) Exposure limits. The...

  7. 29 CFR 1917.24 - Carbon monoxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... using gas detector tube units certified by NIOSH under 30 CFR part 11 or other measuring instruments... 29 Labor 7 2012-07-01 2012-07-01 false Carbon monoxide. 1917.24 Section 1917.24 Labor Regulations...) MARINE TERMINALS Marine Terminal Operations § 1917.24 Carbon monoxide. (a) Exposure limits. The...

  8. 29 CFR 1917.24 - Carbon monoxide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... using gas detector tube units certified by NIOSH under 30 CFR part 11 or other measuring instruments... 29 Labor 7 2010-07-01 2010-07-01 false Carbon monoxide. 1917.24 Section 1917.24 Labor Regulations...) MARINE TERMINALS Marine Terminal Operations § 1917.24 Carbon monoxide. (a) Exposure limits. The...

  9. 29 CFR 1917.24 - Carbon monoxide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... using gas detector tube units certified by NIOSH under 30 CFR part 11 or other measuring instruments... 29 Labor 7 2011-07-01 2011-07-01 false Carbon monoxide. 1917.24 Section 1917.24 Labor Regulations...) MARINE TERMINALS Marine Terminal Operations § 1917.24 Carbon monoxide. (a) Exposure limits. The...

  10. 29 CFR 1917.24 - Carbon monoxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... using gas detector tube units certified by NIOSH under 30 CFR part 11 or other measuring instruments... 29 Labor 7 2013-07-01 2013-07-01 false Carbon monoxide. 1917.24 Section 1917.24 Labor Regulations...) MARINE TERMINALS Marine Terminal Operations § 1917.24 Carbon monoxide. (a) Exposure limits. The...

  11. 40 CFR 600.115-11 - Criteria for determining the fuel economy label calculation method.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... economy label calculation method. 600.115-11 Section 600.115-11 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) ENERGY POLICY FUEL ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.115-11 Criteria...

  12. 40 CFR 600.115-11 - Criteria for determining the fuel economy label calculation method.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... economy label calculation method. 600.115-11 Section 600.115-11 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) ENERGY POLICY FUEL ECONOMY AND GREENHOUSE GAS EXHAUST EMISSIONS OF MOTOR VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.115-11 Criteria...

  13. Pioneer 10 and 11

    NASA Technical Reports Server (NTRS)

    Lozier, D.; Fimmel, R.

    1991-01-01

    The DSN (Deep Space Network) mission support requirements for Pioneer 10 and 11 are summarized. The primary objective of these Pioneer missions is to investigate the interplanetary medium beyond the orbit of Saturn and, in particular, to gather data which may locate the heliopause as these spacecraft cruise out of the solar system to the extreme of their communication capabilities. The mission objectives are outlined and the DSN support requirements are defined through the presentation of tables and narratives describing the spacecraft flight profile; DSN support coverage; frequency assignments; support parameters for telemetry, command and support systems; and tracking support responsibility.

  14. Carbon cyclist

    NASA Astrophysics Data System (ADS)

    Showstack, Randy

    A satellite launched in early August as part of NASA's Mission to Planet Earth could dramatically increase understanding of how carbon cycles through the Earth's biosphere and living organisms and how this process influences global climate. The Sea-viewing Wide Field-of-View Sensor (SeaWiFS) will measure the color of the oceans with a radiometer to determine the concentration of chlorophyll found in oceanic phytoplankton. The single-celled plants, at the base of food chains around the world, remove carbon dioxide from seawater through photosynthesis, which allows oceans to absorb more carbon dioxide from the atmosphere.

  15. Apollo 10 - 11

    NASA Technical Reports Server (NTRS)

    2001-01-01

    This video gives overviews of the Apollo 10 and Apollo 11 missions to the moon, including footage from the launches and landings of the Command Module Columbia, which is used for both flights. The Apollo 10 crewmembers, Commander Thomas Stafford, Command Module Pilot John Young, and Lunar Module Pilot Eugene Cernan, are seen as they suit-up in preparation for launch and then as they experiment with the microgravity environment on their way to the moon. The moon's surface is seen in detail as the Command Module orbits at an altitude of 69 miles. The Apollo 11 crewmembers, Commander Neil Armstrong, Command Module Pilot Michael Collins, and Lunar Module Pilot Buzz Aldrin, are seen during various training activities, including simulated lunar gravity training, practicing collecting lunar material, and using the moonquake detector. Footage shows the approach and landing of the Lunar Module Eagle on the moon. Armstrong and Aldrin descend to the moon's surface, collect a sample of lunar dust, and erect the American flag. Eagle's liftoff from the moon is seen.

  16. Synthesis of C-11-{beta}-aminoisobutyric acid (C-11-{beta}-AlB): A major in vivo catabolite of [methyl-C-11]thymidine

    SciTech Connect

    Alauddin, M.M.; Conti, P.S.; Fissekis, J.D.

    1995-05-01

    Carbon-11 labeled thymidine (TdR) is being used for brain tumor imaging in patients with PET. Following clearance of 5-methyl C-11 TdR from plasma in humans, there is a progressive increase of C-11 activity in normal brain and tumor presumably secondary to accumulation of C-11 beta-AIB, a major by-product of thymidine catabolism in vivo. Canine studies have demonstrated that the major radiolabeled species in acid soluble extracts of brain and tumor tissues during C-14 TdR studies is beta-AIB. The previously reported synthesis of beta-AIB is not suitable for incorporation of carbon-11. A convenient method of synthesis of C-11 beta-AIB was developed where commercially available beta-alanine ethyl ester was converted to the cold precursor reagent, benzaldimine-beta-alanine ethyl ester, in 87% yield. Treatment of the imine derivative with LDA (1.1 eq) in THF at -78{degrees} C, followed by addition of iodomethane (1.1 eq) produced the alpha-methylated benzaldimine-beta-alanine ethyl ester in 73% chemical yield. Deprotection of the amino group by acidic hydrolysis followed by basic hydrolysis of the ester group produced the desired product in 50% chemical yield. Chemical structures of unlabeled intermediates and product were confirmed by H-1 NMR and CI mass spectrometry. Labeling was accomplished using C-11-methyl iodide prepared from C-11-CO{sub 2} according to literature methods. After removal of protecting groups and neutralization, the enatiomeric mixture was purified by HPLC using a semipreparative reverse phase C-18 column and PBS as eluent. The desired compound was eluted at 8.26 minutes. In preliminary runs, the synthesis time was 39 minutes including HPLC purification, with radiochemical yields of 5-6% (EOB). Radiochemical purity was >99%

  17. Calcium Carbonate.

    PubMed

    Al Omari, M M H; Rashid, I S; Qinna, N A; Jaber, A M; Badwan, A A

    2016-01-01

    Calcium carbonate is a chemical compound with the formula CaCO3 formed by three main elements: carbon, oxygen, and calcium. It is a common substance found in rocks in all parts of the world (most notably as limestone), and is the main component of shells of marine organisms, snails, coal balls, pearls, and eggshells. CaCO3 exists in different polymorphs, each with specific stability that depends on a diversity of variables.

  18. Calcium Carbonate.

    PubMed

    Al Omari, M M H; Rashid, I S; Qinna, N A; Jaber, A M; Badwan, A A

    2016-01-01

    Calcium carbonate is a chemical compound with the formula CaCO3 formed by three main elements: carbon, oxygen, and calcium. It is a common substance found in rocks in all parts of the world (most notably as limestone), and is the main component of shells of marine organisms, snails, coal balls, pearls, and eggshells. CaCO3 exists in different polymorphs, each with specific stability that depends on a diversity of variables. PMID:26940168

  19. Developments in carbon materials

    NASA Technical Reports Server (NTRS)

    Burchell, Timothy D.

    1994-01-01

    The following carbon-based materials are reviewed and their applications discussed: fullerenes; graphite (synthetic and manufactured); activated carbon fibers; and carbon-carbon composites. Carbon R&D activities at ORNL are emphasized.

  20. Single carbon nanotube photovoltaic device

    NASA Astrophysics Data System (ADS)

    Barkelid, M.; Zwiller, V.

    2013-10-01

    Here we present photocurrent measurements on a single suspended carbon nanotube p-n junction. The p-n junction was induced by electrostatic doping by local gates, and the E11 and E22 resonances in the nanotube could be probed using photocurrent spectroscopy. Current-voltage characteristics were recorded, revealing an enhanced optoelectronic response on resonance. The internal power conversion efficiency for the nanotube diode was extracted on and off resonance with the E11 and E22, and a large internal power conversion efficiency was observed. An internal efficiency of up to 23% is reported for the E11, showing the potential of carbon nanotubes to be used as the active element in photovoltaic devices. Finally, a photovoltaic device is proposed which exploits this enhanced efficiency.

  1. 40 CFR 721.10287 - Infused carbon nanostructures (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Infused carbon nanostructures (generic... Specific Chemical Substances § 721.10287 Infused carbon nanostructures (generic). (a) Chemical substance... infused carbon nanostructures (PMN P-11-188) is subject to reporting under this section for...

  2. 40 CFR 721.10287 - Infused carbon nanostructures (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Infused carbon nanostructures (generic... Specific Chemical Substances § 721.10287 Infused carbon nanostructures (generic). (a) Chemical substance... infused carbon nanostructures (PMN P-11-188) is subject to reporting under this section for...

  3. 40 CFR 721.10287 - Infused carbon nanostructures (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Infused carbon nanostructures (generic... Specific Chemical Substances § 721.10287 Infused carbon nanostructures (generic). (a) Chemical substance... infused carbon nanostructures (PMN P-11-188) is subject to reporting under this section for...

  4. 40 CFR 721.10099 - Dialkyl dimethyl ammonium carbonate (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Dialkyl dimethyl ammonium carbonate... Specific Chemical Substances § 721.10099 Dialkyl dimethyl ammonium carbonate (generic). (a) Chemical... as dialkyl dimethyl ammonium carbonate (1:1) (PMN P-03-715) is subject to reporting under...

  5. 40 CFR 721.10099 - Dialkyl dimethyl ammonium carbonate (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Dialkyl dimethyl ammonium carbonate... Specific Chemical Substances § 721.10099 Dialkyl dimethyl ammonium carbonate (generic). (a) Chemical... as dialkyl dimethyl ammonium carbonate (1:1) (PMN P-03-715) is subject to reporting under...

  6. Infiltrated carbon foam composites

    NASA Technical Reports Server (NTRS)

    Lucas, Rick D. (Inventor); Danford, Harry E. (Inventor); Plucinski, Janusz W. (Inventor); Merriman, Douglas J. (Inventor); Blacker, Jesse M. (Inventor)

    2012-01-01

    An infiltrated carbon foam composite and method for making the composite is described. The infiltrated carbon foam composite may include a carbonized carbon aerogel in cells of a carbon foam body and a resin is infiltrated into the carbon foam body filling the cells of the carbon foam body and spaces around the carbonized carbon aerogel. The infiltrated carbon foam composites may be useful for mid-density ablative thermal protection systems.

  7. 40 CFR 86.201-11 - General applicability.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ...-Duty Passenger Vehicles; Cold Temperature Test Procedures § 86.201-11 General applicability. (a) This subpart describes procedures for determining the cold temperature carbon monoxide (CO) emissions from 1994... provisions of this subpart are applicable to testing conducted at a nominal temperature of 20 °F (−7 °C)....

  8. 11 CFR 9033.11 - Documentation of disbursements.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... or authorized committee(s) are qualified campaign expenses as defined in 11 CFR 9032.9. The candidate... of acceptable and unacceptable descriptions of goods and services purchased are listed at 11 CFR 104.3(b)(3)(i)(B). (4) The documentation requirements of 11 CFR 102.9(b) shall also apply...

  9. 11. Historic view, Pier 11. View to north, showing concrete ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    11. Historic view, Pier 11. View to north, showing concrete pier under construction, 1956. Photographic copy of photo. Boston National Historical Park Archives, Charlestown Navy Yard. - Charlestown Navy Yard, Pier 11, Charlestown Waterfront at confluence of Little Mystic Channel & Mystic River at northernmost ent of Navy Yard, Boston, Suffolk County, MA

  10. 11 CFR 9033.11 - Documentation of disbursements.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... of acceptable and unacceptable descriptions of goods and services purchased are listed at 11 CFR 104.3(b)(3)(i)(B). (4) The documentation requirements of 11 CFR 102.9(b) shall also apply to... or authorized committee(s) are qualified campaign expenses as defined in 11 CFR 9032.9. The...

  11. Aquaporin-11 (AQP11) Expression in the Mouse Brain

    PubMed Central

    Koike, Shin; Tanaka, Yasuko; Matsuzaki, Toshiyuki; Morishita, Yoshiyuki; Ishibashi, Kenichi

    2016-01-01

    Aquaporin-11 (AQP11) is an intracellular aquaporin expressed in various tissues, including brain tissues in mammals. While AQP11-deficient mice have developed fatal polycystic kidneys at one month old, the role of AQP11 in the brain was not well appreciated. In this study, we examined the AQP11 expression in the mouse brain and the brain phenotype of AQP11-deficient mice. AQP11 messenger ribonucleic acid (mRNA) and protein were expressed in the brain, but much less than in the thymus and kidney. Immunostaining showed that AQP11 was localized at the epithelium of the choroid plexus and at the endothelium of the brain capillary, suggesting that AQP11 may be involved in water transport at the choroid plexus and blood-brain barrier (BBB) in the brain. The expression of AQP4, another brain AQP expressed at the BBB, was decreased by half in AQP11-deficient mice, thereby suggesting the presence of the interaction between AQP11 and AQP4. The brain of AQP11-deficient mice, however, did not show any morphological abnormalities and the function of the BBB was intact. Our findings provide a novel insight into a water transport mechanism mediated by AQPs in the brain, which may lead to a new therapy for brain edema. PMID:27258268

  12. 11 CFR 9033.11 - Documentation of disbursements.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... or authorized committee(s) are qualified campaign expenses as defined in 11 CFR 9032.9. The candidate... of acceptable and unacceptable descriptions of goods and services purchased are listed at 11 CFR 104.3(b)(3)(i)(B). (4) The documentation requirements of 11 CFR 102.9(b) shall also apply...

  13. 11 CFR 114.11 - Employee participation plans.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 11 Federal Elections 1 2010-01-01 2010-01-01 false Employee participation plans. 114.11 Section 114.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL CORPORATE AND LABOR ORGANIZATION ACTIVITY... including members of a labor organization who are employees of the corporation. Communications...

  14. Biological activation of carbon filters.

    PubMed

    Seredyńska-Sobecka, Bozena; Tomaszewska, Maria; Janus, Magdalena; Morawski, Antoni W

    2006-01-01

    To prepare biological activated carbon (BAC), raw surface water was circulated through granular activated carbon (GAC) beds. Biological activity of carbon filters was initiated after about 6 months of filter operation and was confirmed by two methods: measurement of the amount of biomass attached to the carbon and by the fluorescein diacetate (FDA) test. The effect of carbon pre-washing on WG-12 carbon properties was also studied. For this purpose, the nitrogen adsorption isotherms at 77K and Fourier transform-infrared (FT-IR) spectra analyses were performed. Moreover, iodine number, decolorizing power and adsorption properties of carbon in relation to phenol were studied. Analysis of the results revealed that after WG-12 carbon pre-washing its BET surface increased a little, the pH value of the carbon water extract decreased from 11.0 to 9.4, decolorizing power remained at the same level, and the iodine number and phenol adsorption rate increased. In preliminary studies of the ozonation-biofiltration process, a model phenol solution with concentration of approximately 10mg/l was applied. During the ozonation process a dose of 1.64 mg O(3)/mg TOC (total organic carbon) was employed and the contact time was 5 min. Four empty bed contact times (EBCTs) in the range of 2.4-24.0 min were used in the biofiltration experiment. The effectiveness of purification was measured by the following parameters: chemical oxygen demand (COD(Mn)), TOC, phenol concentration and UV(254)-absorbance. The parameters were found to decrease with EBCT. PMID:16376966

  15. Carbon sequestration.

    PubMed

    Lal, Rattan

    2008-02-27

    Developing technologies to reduce the rate of increase of atmospheric concentration of carbon dioxide (CO2) from annual emissions of 8.6PgCyr-1 from energy, process industry, land-use conversion and soil cultivation is an important issue of the twenty-first century. Of the three options of reducing the global energy use, developing low or no-carbon fuel and sequestering emissions, this manuscript describes processes for carbon (CO2) sequestration and discusses abiotic and biotic technologies. Carbon sequestration implies transfer of atmospheric CO2 into other long-lived global pools including oceanic, pedologic, biotic and geological strata to reduce the net rate of increase in atmospheric CO2. Engineering techniques of CO2 injection in deep ocean, geological strata, old coal mines and oil wells, and saline aquifers along with mineral carbonation of CO2 constitute abiotic techniques. These techniques have a large potential of thousands of Pg, are expensive, have leakage risks and may be available for routine use by 2025 and beyond. In comparison, biotic techniques are natural and cost-effective processes, have numerous ancillary benefits, are immediately applicable but have finite sink capacity. Biotic and abiotic C sequestration options have specific nitches, are complementary, and have potential to mitigate the climate change risks. PMID:17761468

  16. 46 CFR 11.107 - Paperwork approval.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... GUARD, DEPARTMENT OF HOMELAND SECURITY MERCHANT MARINE OFFICERS AND SEAMEN REQUIREMENTS FOR OFFICER... to the sections indicated: (1) OMB 1625-0040-46 CFR 11.201, 11.202, 11.205, 11.470, 11.472, 11.474, 11.542, and 11.544. (2) OMB 1625-028-46 CFR 11.302, 11.303, 11.304, 11.480. (3) OMB 1625-0079-46...

  17. Carbon particles

    DOEpatents

    Hunt, Arlon J.

    1984-01-01

    A method and apparatus whereby small carbon particles are made by pyrolysis of a mixture of acetylene carried in argon. The mixture is injected through a nozzle into a heated tube. A small amount of air is added to the mixture. In order to prevent carbon build-up at the nozzle, the nozzle tip is externally cooled. The tube is also elongated sufficiently to assure efficient pyrolysis at the desired flow rates. A key feature of the method is that the acetylene and argon, for example, are premixed in a dilute ratio, and such mixture is injected while cool to minimize the agglomeration of the particles, which produces carbon particles with desired optical properties for use as a solar radiant heat absorber.

  18. Commissioned Review. Carbon: freshwater plants

    USGS Publications Warehouse

    Keeley, J.E.; Sandquist, D.R.

    1992-01-01

    δ13C values for freshwater aquatic plant matter varies from −11 to −50‰ and is not a clear indicator of photosynthetic pathway as in terrestrial plants. Several factors affect δ13C of aquatic plant matter. These include: (1) The δ13C signature of the source carbon has been observed to range from +1‰ for HCO3− derived from limestone to −30‰ for CO2 derived from respiration. (2) Some plants assimilate HCO3−, which is –7 to –11‰ less negative than CO2. (3) C3, C4, and CAM photosynthetic pathways are present in aquatic plants. (4) Diffusional resistances are orders of magnitude greater in the aquatic environment than in the aerial environment. The greater viscosity of water acts to reduce mixing of the carbon pool in the boundary layer with that of the bulk solution. In effect, many aquatic plants draw from a finite carbon pool, and as in terrestrial plants growing in a closed system, biochemical discrimination is reduced. In standing water, this factor results in most aquatic plants having a δ13C value similar to the source carbon. Using Farquhar's equation and other physiological data, it is possible to use δ13C values to evaluate various parameters affecting photosynthesis, such as limitations imposed by CO2 diffusion and carbon source.

  19. Manual of carbonate sedimentology

    SciTech Connect

    Reijers, T.J.; Hsu, K.S.

    1986-01-01

    This manual, organised along encycolopaedic/lexicographic lines, summarizes information on the properties and characteristics of carbonates and their environments. Part 1 deals with the elements of carbonates; Part 2 with environments, settings, and carbonate bodies; Part 3 with carbonate diagenesis, and Part 4 with carbonate reservoirs. Contents include: Elements of carbonates; Carbonate Environments, Settings and Bodies; Carbonate diagenesis; Carbonate reservoirs; Alphabetical Indices; English, Dutch, German, Spanish, French Computer Compatible Codes; Commonly Used (Informal) abbreviations.

  20. From Kelvin problem to Kelvin carbons.

    PubMed

    Zhao, Hui-Yan; Wang, Jing; Ma, Qing-Min; Liu, Ying

    2013-04-28

    As children's toys, soap bubbles also underpin many important scientific questions. What is the most efficient structure for foam? - the "Kelvin problem," has been one of the most intriguing science and widely discussed over the past hundred years. Soap bubbles' frameworks have similar topology with sp(3)-bonded carbon or silicon allotropes, e.g., Weaire-Phelan foam and superconducting clathrate Na8Si46. By looking at the most efficient structure for foams, we construct a series of new carbon allotropes, named "Kelvin carbons." Unexpectedly, all 11 Kelvin carbons are structurally stable wide-bandgap semiconductors, and their densities and their intrinsic hardnesses are both about 81%-87% that of diamond. The seventh state of Kelvin carbons, K(VII), is a very low energy carbon structure after graphite, diamond, lonsdaleite, and type-II carbon clathrate. Kelvin carbons, which constitute a "bridge" between macro-foams and micro-carbons, together with recently proposed novel carbon phases can enrich the study of carbon allotropes. PMID:23635161

  1. From Kelvin problem to Kelvin carbons

    NASA Astrophysics Data System (ADS)

    Zhao, Hui-Yan; Wang, Jing; Ma, Qing-Min; Liu, Ying

    2013-04-01

    As children's toys, soap bubbles also underpin many important scientific questions. What is the most efficient structure for foam? - the "Kelvin problem," has been one of the most intriguing science and widely discussed over the past hundred years. Soap bubbles' frameworks have similar topology with sp3-bonded carbon or silicon allotropes, e.g., Weaire-Phelan foam and superconducting clathrate Na8Si46. By looking at the most efficient structure for foams, we construct a series of new carbon allotropes, named "Kelvin carbons." Unexpectedly, all 11 Kelvin carbons are structurally stable wide-bandgap semiconductors, and their densities and their intrinsic hardnesses are both about 81%-87% that of diamond. The seventh state of Kelvin carbons, KVII, is a very low energy carbon structure after graphite, diamond, lonsdaleite, and type-II carbon clathrate. Kelvin carbons, which constitute a "bridge" between macro-foams and micro-carbons, together with recently proposed novel carbon phases can enrich the study of carbon allotropes.

  2. Carbon disulfide

    Integrated Risk Information System (IRIS)

    Carbon disulfide ; CASRN 75 - 15 - 0 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic E

  3. Carbon tetrachloride

    Integrated Risk Information System (IRIS)

    Carbon tetrachloride ; CASRN 56 - 23 - 5 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogen

  4. (/sup 11/C)clorgyline and (/sup 11/C)-L-deprenyl and their use in measuring functional monoamine oxidase activity in the brain using positron emission tomography

    DOEpatents

    Fowler, J.S.; MacGregor, R.R.; Wolf, A.P.

    1986-04-17

    This invention involves a new strategy for imaging the activity of the enzyme monoamine oxidase in the living body by using /sup 11/C-labeled enzyme inhibitors which bind irreversibly to an enzyme as a result of catalysis. By using positron emission tomography to image the distribution of radioactivity produced by the body penetrating radiation emitted by carbon-11, a map of functionally active monoamine oxidase activity is obtained. Clorgyline and L-deprenyl are suicide enzyme inhibitors and irreversibly inhibit monoamine oxidase. When these inhibitors are labeled with carbon-11 they provide selective probes for monoamine oxidase localization and reactivity in vivo using positron emission tomography. 2 figs.

  5. Oxidation protected carbon-carbon

    NASA Technical Reports Server (NTRS)

    Pavlosky, J. E.; St. Leger, L. G.

    1972-01-01

    Pyrolized carbon-carbon has one unique advantage over other materials that makes its application to the space shuttle thermal protection system very attractive. This unique characteristic is the increase in material strength and modulus with increase in temperature up to about 2500 K (4040 F). Offsetting this unique advantage are disadvantages which include brittleness, high cost, and the tendency of the material to react with oxygen, particularly at high temperatures. The development of an oxidation inhibitor for the material and the definition of fabrication processes for selected full-scale components are considered.

  6. Development of additive [11C]CO2 target system in the KOTRON-13 cyclotron and its application for [11C]radiopharmaceutical production

    NASA Astrophysics Data System (ADS)

    Moon, Byung Seok; Lee, Hong Jin; Lee, Won Kyung; Hur, Min Goo; Yang, Seung Dae; Lee, Byung Chul; Kim, Sang Eun

    2015-08-01

    The KOTRON-13 cyclotron, which was developed in South Korea for the production of medical radioisotopes, has the structural limitation of only one beam-output port, restricting the production of the carbon-11 isotope. In the present study, we investigate the design of a switchable target system and develop an effective carbon-11 target in the KOTRON-13 cyclotron, for combination with the fluorine-18 target. The target system was designed by introducing a sliding-type element between the fluorine-18 and carbon-11 targets, a tailor-made C-11 target and its cooling system. For the efficient production of [11C]CO2, the desirable target shape and internal volume were determined by a Stopping and Range of Ions in Matter (SRIM) simulation program, and the target grid was modified to resist the cavity pressure during beam irradiation. We evaluated the [11C]CO2 production while varying the material and thickness of the target foil, oxygen content of the nitrogen gas, and target loading pressure. Using sliding-type equipment including an additional gate valve and a high vacuum in a beam line, the bi-directional conversion between the fluorine-18 and carbon-11 targets was efficient regarding the accurate beam irradiation on both targets. The optimal [11C]CO2 production for 30 min irradiation at 60 μA (86.6 ± 1.7 GBq in the target at EOB) was observed at a thickness of 19 μm with HAVAR® material as a target foil and a target loading pressure of 24 bar with nitrogen plus 300 ppb of oxygen gas. Additionally, the coolant cavity system in the target grid and target chamber is useful to remove the heat transferred to the target body by the internal convection of water and thereby ensure the stability of the [11C]CO2 production under a high beam current. In the application of C-11 labeled radiopharmaceuticals such as [11C]PIB, [11C]DASB, [11C]PBR28, [11C]Methionine and [11C]Clozapine, the radiochemical yields were shown to be 25-38% (decay corrected) with over 166 GBq/μmol of

  7. Carbon/Carbon Grids For Ion Sources

    NASA Technical Reports Server (NTRS)

    Garner, Charles E.

    1995-01-01

    Ion-extraction grids made of carbon/carbon composites used in spacecraft ion engines and industrial ion sources in place of molybdenum grids. In principle, carbon/carbon grids offer greater extraction efficiency and longer life. Grid fabricated by mechanical drilling, laser drilling, or electrical-discharge machining of array of holes in sheet of carbon/carbon. Advantages; better alignment and slower erosion.

  8. Carbon recycling in ophiolite-hosted carbonates, Oman-UAE

    NASA Astrophysics Data System (ADS)

    Stephen, A.; Jenkin, G. R.; Smith, D. J.; Styles, M. T.; Naden, J.; Boyce, A. J.; Bryant, C. L.

    2013-12-01

    Large-scale surface and subsurface freshwater carbonate deposits of probable Quaternary age have formed on the Oman-UAE ophiolite. Here, serpentinisation reactions in ultramafic rocks have produced calcite and magnesite. These carbonates are frequently cited as examples of natural atmospheric CO2 sequestration, but the possibility of carbon recycling has not been addressed. The aim of this study is to assess the degree of atmospheric CO2 being incorporated into carbonates versus that which has been recycled from alternative sources such as soil CO2, or limestones that underlie the ophiolite. This has been determined through δ13C/δ18O, 87Sr/86Sr and 14C analysis of all major carbonate lithofacies identified. Our analyses of modern carbonate crusts forming on the surface of stagnant hyperalkaline (pH >11) waters show highly depleted δ13C and δ18O values (-25.5‰ ×0.5 PDB and -16.8‰ ×0.5 PDB respectively). This depletion has been attributed to a kinetic isotope effect occurring during atmospheric CO2 exchange with Ca(OH)2 hyperalkaline waters [1]. By comparison, inactive travertine deposits show a large range in δ13C (-10.5 to -21.8‰ PDB) which lies on a trajectory from the composition of modern crusts towards bicarbonate fluids in equilibrium with soil CO2. We interpret this trend as being produced by the mixing of different carbon sources, either at the time of formation or during later alteration. Modern carbonates and inactive travertines also have 87Sr/86Sr ratios and Sr concentrations similar to Cretaceous and Tertiary limestones which surround the ophiolite, whilst subsurface veins also display 87Sr/86Sr ratios similar to these Cretaceous limestones. Carbon recycling can also be determined with 14C. Modern atmospheric CO2 has a global average of 105-106% modern 14C (pMC), therefore freshwater carbonates forming solely from atmospheric CO2 would be expected to contain >100 pMC. However, modern carbonates display varied results from 94.5-101.4 p

  9. Biosynthesis of glycerol carbonate from glycerol by lipase in dimethyl carbonate as the solvent.

    PubMed

    Lee, Kyung Hwa; Park, Chang-Ho; Lee, Eun Yeol

    2010-11-01

    Glycerol carbonate was synthesized from renewable glycerol and dimethyl carbonate using lipase in solvent-free reaction system in which excess dimethyl carbonate played as the reaction medium. A variety of lipases have been tested for their abilities to catalyze transesterification reaction, and Candida antartica lipase B and Novozyme 435 exhibited higher catalytic activities. The silica-coated glycerol with a 1:1 ratio was supplied to prevent two-phase formation between hydrophobic dimethyl carbonate and hydrophilic glycerol. Glycerol carbonate was successfully synthesized with more than 90% conversion from dimethyl carbonate and glycerol with a molar ratio of 10 using Novozyme 435-catalyzed transesterification at 70 °C. The Novozyme 435 [5% (w/w) and 20% (w/w)] and silica gel were more than four times recycled with good stability in a repeated batch operation for the solvent-free synthesis of glycerol carbonate. PMID:20502921

  10. Biosynthesis of glycerol carbonate from glycerol by lipase in dimethyl carbonate as the solvent.

    PubMed

    Lee, Kyung Hwa; Park, Chang-Ho; Lee, Eun Yeol

    2010-11-01

    Glycerol carbonate was synthesized from renewable glycerol and dimethyl carbonate using lipase in solvent-free reaction system in which excess dimethyl carbonate played as the reaction medium. A variety of lipases have been tested for their abilities to catalyze transesterification reaction, and Candida antartica lipase B and Novozyme 435 exhibited higher catalytic activities. The silica-coated glycerol with a 1:1 ratio was supplied to prevent two-phase formation between hydrophobic dimethyl carbonate and hydrophilic glycerol. Glycerol carbonate was successfully synthesized with more than 90% conversion from dimethyl carbonate and glycerol with a molar ratio of 10 using Novozyme 435-catalyzed transesterification at 70 °C. The Novozyme 435 [5% (w/w) and 20% (w/w)] and silica gel were more than four times recycled with good stability in a repeated batch operation for the solvent-free synthesis of glycerol carbonate.

  11. Equation of State of Carbonated Hydroxylapatite at Ambient Temperature up to 10 GPa: Significance of Carbonate

    SciTech Connect

    X Liu; S Shieh; M Fleet; L Zhang; Q He

    2011-12-31

    The incorporation of the carbonate ion into the crystal structure of hydroxylapatite results in the creation of vacancies, oxygen-loss, and disorder, with consequent changes in physical and chemical properties. High-pressure experimental investigation up to 10 GPa of two synthetic carbonated hydroxylapatite samples with up to 11 wt% CO3, using a diamond-anvil cell and synchrotron powder X-ray diffraction, provides the first rigorous assessment of the mechanical behavior of the carbonated hydroxylapatite. The pressure-volume data suggest that the isothermal bulk modulus of these carbonated hydroxylapatites has been significantly decreased by the presence of the carbonate (up to about 15%), which in turn will affect all the carbonated apatite-related reactions in the geosystem. Since hydroxylapatite is one of the major components of the bones and teeth, the incorporation of the carbonate in the hydroxylapatite weakens teeth and bones not only chemically, but also physically.

  12. 1,1-Dichloroethylene (1,1-DCE)

    Integrated Risk Information System (IRIS)

    1,1 - Dichloroethylene ( 1,1 - DCE ) ; CASRN 75 - 35 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments f

  13. 11. Photograph of a line drawing. SHEET 11, LONGITUDINAL SECTION ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    11. Photograph of a line drawing. SHEET 11, LONGITUDINAL SECTION ON LINE FF; 9-16-1940. Assembly Building for Tank Plant for the Chrysler Corporation, Macomb County, Michigan. Delineator: E.B. - Detroit Arsenal, 6501 East Eleven Mile Road, Warren, Macomb County, MI

  14. 19. MANHOLE ON 9 ' 0' X 11' 0' 11 ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    19. MANHOLE ON 9 ' 0' X 11' 0' 11 ' 0' SEWER, SECTIONS. SHEET 3 OF 3. CASE A, DRAWING 784. - Mile Rock Tunnel, Under Forty-eighth Avenue from Cabrillo Street to San Francisco Bay at Point Lobos, San Francisco, San Francisco County, CA

  15. Enzymatic synthesis of C-11 formaldehyde: concise communication

    SciTech Connect

    Slegers, G.; Lambrecht, R.H.D.; Vandewalle, T.; Meulewaeter, L.; Vandecasteele, C.

    1984-03-01

    An enzymatic synthesis of C-11 formaldehyde from C-11 methanol is presented, with immobilized alcohol oxidase and catalase: a rapid, simple procedure, with a high and reproducible yield. Carbon-11 methanol is oxidized to C-11 formaldehyde by passage over a column on which the enzymes alcohol oxidase and catalase are immobilized. The catalase increases reaction velocity by recycling the oxygen, and prevents destruction of the alcohol oxidase by eliminating the excess of hydrogen peroxide. The yield of the enzyme-catalyzed oxidation was 80-95%. A specific activity of 400-450 mCi/..mu..mole was obtained at EOB + 20 min. Various immobilization techniques and the optimal reaction conditions of the immobilized enzymes are investigated.

  16. Maintenance Downtime March 11, 2015

    Atmospheric Science Data Center

    2015-03-09

    Date(s):  Wednesday, March 11, 2015 Time:  06:00 - 01:00 pm EDT Event ... Connectivity to the Eosweb site will be unavailable from 9 - 11 am. • The Data Pool, MISR order and browse tools, TES and MOPITT ...

  17. Maintenance Downtime February 11, 2015

    Atmospheric Science Data Center

    2015-02-13

    Date(s):  Wednesday, February 11, 2015 Time:  07:00 am - TBD EST Event Impact:  ... Connectivity to the Eosweb site will be unavailable from 9 - 11 am.  * ( returned to service by 9:30 am )   ...

  18. C-11 cyanide production system

    DOEpatents

    Kim, Dohyun; Alexoff, David; Kim, Sung Won; Hooker, Jacob; Ferrieri, Richard A

    2015-01-13

    A method for providing .sup.11C-labeled cyanides from .sup.11C labeled oxides in a target gas stream retrieved from an irradiated high pressure gaseous target containing O.sub.2 is provided, wherein .sup.11C labeled oxides are reduced with H.sub.2 in the presence of a nickel catalyst under a pressure and a temperature sufficient to form a product stream comprising at least about 95% .sup.11CH.sup.4 , the .sup.11CH.sub.4 is then combined with an excess of NH.sub.3 in a carrier/reaction stream flowing at an accelerated velocity and the combined .sup.11CH4 carrier/reaction stream is then contacted with a platinum (Pt) catalyst particulate supported on a substantially-chemically-nonreactive heat-stable support at a temperature of at least about 900 .degree. C., whereby a product stream comprising at least about 60%H.sup.11CN is provided in less than 10 minutes from retrieval of the .sup.11C labeled oxide.

  19. Engine makers tap carbon-carbon pistons

    SciTech Connect

    Ashley, S.

    1994-05-01

    This article describes the use of a carbon-carbon composite, developed for nose cones and rocket nozzles, for pistons in modern internal combustion engines. The topics of the article include the carbon-carbon composite mechanical and physical characteristics, initial research, manufacturing methods, fabrication techniques, initial testing in 2 stroke and 4 stroke engines, and current research.

  20. (Inorganic carbon surveys of oceanic basins)

    SciTech Connect

    Wilke, R.J.

    1991-04-25

    Measurements were made aboard the F. S. Meteor, along the 19 degree South cruise track of the following chemical parameters: total dissolved inorganic carbon, pH, pCO2, CFC-12, CFC-11, CFC-113, CC14. This was the first cruise of OASD's newly formed CO2 group. The purpose was to survey World Ocean Circulation Experiment (WOCE) line A9 for inorganic carbon for the Department of Energy's Office of CO2 Research. 1 fig.

  1. Carbon investment funds

    SciTech Connect

    2007-01-15

    The report is a study of the development of funds to invest in the purchase of carbon credits. It takes a look at the growing market for carbon credits, the rise of carbon investment funds, and the current state of carbon investing. Topics covered in the report include: Overview of climate change, greenhouse gases, and the Kyoto Protocols. Analysis of the alternatives for reducing carbon emissions including nitrous oxide reduction, coal mine methane capture and carbon capture and storage; Discussion of the different types of carbon credits; Discussion of the basics of carbon trading; Evaluation of the current status of carbon investing; and Profiles of 37 major carbon investment funds worldwide.

  2. Double elimination protocol for synthesis of 5,6,11,12-tetradehydrodibenzo[a,e]cyclooctene.

    PubMed

    Orita, Akihiro; Hasegawa, Daiki; Nakano, Takehiko; Otera, Junzo

    2002-05-01

    A new method for constructing 5,6,11,12-tetradehydrodibenzo[a,e]cyclooctene is described on the basis of one-pot double elimination protocol. The target molecule, which is the smallest cyclophane with alternate arylene-ethynylene linkage, is synthesized in 61 % yield through oxidative dimerization of ortho-(phenylsulfonylmethyl)benzaldehyde. The initial carbon-carbon bond formation between sp(3) carbons followed by stepwise conversion to sp(2) and finally sp carbons bypasses the difficulty encountered in direct coupling of the sp carbon in the terminal acetylene. The mechanism of this process is discussed. The Wittig-Horner-type coupling is a key reaction employed for the carbon-carbon bond formation. Generation of (E)-vinylsulfone moiety in the first coupling between alpha-sulfonyl anion and aldehyde functions is crucial for the effective second coupling to complete the cyclization. The syn-elimination of the (E)-vinylsulfone moieties in the cyclized intermediate furnishes the acetylenic bonds.

  3. 37 CFR 11.61 - Savings clause.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... been subject to disciplinary action before September 15, 2008. (c) Sections 11.24, 11.25, 11.28 and 11... September 15, 2008. (d) Sections 11.58 through 11.60 shall apply to all cases in which an order of... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Savings clause. 11.61...

  4. BOREAS TF-11 Biomass Data over the SSA-Fen

    NASA Technical Reports Server (NTRS)

    Valentine, David W.; Hall, Forrest G. (Editor); Conrad, Sara (Editor)

    2000-01-01

    The BOREAS TF-11 team collected several data sets in its efforts to fully describe the flux and site characteristics at the SSA-Fen site. This data set contains plant cover, standing crop of plant biomass, and estimated net primary productivity at each chamber site at the end of the 1994 field season. The measurements were conducted as part of a 2 x 2 factorial experiment in which we added carbon (300 g/sq m as wheat straw) and nitrogen (6 g/sq m as urea) to four replicate locations in the vicinity of the TF-11 tower. The data are stored in tabular ASCII files.

  5. BOREAS TF-11 Decomposition Data over the SSA-Fen

    NASA Technical Reports Server (NTRS)

    Valentine, David W.; Hall, Forrest G. (Editor); Conrad, Sara (Editor)

    2000-01-01

    The BOREAS TF-11 team collected several data sets in its efforts to fully describe the flux and site characteristics at the SSA-Fen site. This data set contains decomposition rates of a standard substrate (wheat straw) across treatments. The measurements were conducted in 1994 as part of a 2 x 2 factorial experiment in which we added carbon (300 g/sq m as wheat straw) and nitrogen (6 g/sq m as urea) to four replicate locations in the vicinity of the TF-11 tower. The data are stored in tabular ASCII files.

  6. 27 CFR 11.11 - Meaning of terms.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ..., Delegation of the Administrator's Authorities in 27 CFR Part 11, Consignment Sales. Exchange. The transfer of..., rectifier, blender, or other producer, or as an importer or wholesaler of distilled spirits, wine or...

  7. 27 CFR 11.11 - Meaning of terms.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ..., Delegation of the Administrator's Authorities in 27 CFR Part 11, Consignment Sales. Exchange. The transfer of..., rectifier, blender, or other producer, or as an importer or wholesaler of distilled spirits, wine or...

  8. Target design considerations for high specific activity [{sup 11}C]O{sub 2}

    SciTech Connect

    Ferrieri, R.A.; Alexoff, D.L.; Schlyer, D.J.; McDonald, K.; Wolf, A.P.

    1993-12-31

    In the routine preparation of {sup 11}C-labeled compounds through N-[{sup 11}C]-methylation using [{sup 11}C]H{sub 3}I, total masses are always higher than synthesis mass contribution, suggesting that the target system contributes carrier carbon to the final product mass. This conclusion prompted this evaluation of target materials and target design for [{sup 11}C]O{sub 2} production. Ultimately, one is faced with the sprospect of compromising between [{sup 11}C]O{sub 2} specific activity and the amount that can be extracted from the target after a reasonable irradiation time.

  9. 40 CFR 458.11 - Specialized definitions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Furnace Process... shall apply to this subpart. (b) The term “product” shall mean carbon black manufactured by the...

  10. 40 CFR 458.11 - Specialized definitions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Furnace Process... shall apply to this subpart. (b) The term “product” shall mean carbon black manufactured by the...

  11. APOLLO 11: The heroes Return

    NASA Technical Reports Server (NTRS)

    1974-01-01

    The crew of APOLLO 11 return as heroes after their succesfull landing on the lunar surface. From the film documentary 'APOLLO 11:'The Eagle Has Landed'', part of a documentary series on the APOLLO missions made in the early '70's and narrated by Burgess Meredith. APOLLO 11: First manned lunar landing and return to Earth with Neil A. Armstrong, Michael Collins, and Edwin E. Aldrin. Landed in the Sea of Tranquilityon July 20, 1969; deployed TV camera and EASEP experiments, performed lunar surface EVA, returned lunar soil samples. Mission Duration 195 hrs 18 min 35sec

  12. Synthesis, isolation and purification of [11C]-choline

    PubMed Central

    Jadwiński, Michał; Chmura, Agnieszka; Gorczewski, Kamil; Sokół, Maria

    2016-01-01

    [11C]-choline is an effective PET tracer used for imaging of neoplastic lesions and metastases of the prostate cancer. However, its production can be a challenge for manufacturers, as it has not yet been described in Polish or European pharmacopoeia. In this study the technical aspects of [11C]-choline production are described and detailed process parameters are provided. The quality control procedures for releasing [11C]-choline as solutio iniectabilis are also presented. The purity and quality of the radiopharmaceutical obtained according to the proposed method were find to be high enough to safely administrate the radiopharmaceutical to patients. Application of an automated synthesizer makes it possible to carry out the entire process of [11C]-choline production, isolation and purification within 20 minutes. It is crucial to maintain all aspects of the process as short as possible, since the decay half-time of carbon-11 is 20.4 minutes. The resulting radiopharmaceutical is sterile and pyrogen-free and of a high chemical, radiochemical, and radionuclide purity proved by chromatographic techniques. The yield of the process is up to 20%. [11C]-choline PET scanning can be used as accurate and effective diagnostic tool in all centers equipped with [11C]-target containing cyclotron.

  13. Synthesis, isolation and purification of [(11)C]-choline.

    PubMed

    Szydło, Marcin; Jadwiński, Michał; Chmura, Agnieszka; Gorczewski, Kamil; Sokół, Maria

    2016-01-01

    [(11)C]-choline is an effective PET tracer used for imaging of neoplastic lesions and metastases of the prostate cancer. However, its production can be a challenge for manufacturers, as it has not yet been described in Polish or European pharmacopoeia. In this study the technical aspects of [(11)C]-choline production are described and detailed process parameters are provided. The quality control procedures for releasing [(11)C]-choline as solutio iniectabilis are also presented. The purity and quality of the radiopharmaceutical obtained according to the proposed method were find to be high enough to safely administrate the radiopharmaceutical to patients. Application of an automated synthesizer makes it possible to carry out the entire process of [(11)C]-choline production, isolation and purification within 20 minutes. It is crucial to maintain all aspects of the process as short as possible, since the decay half-time of carbon-11 is 20.4 minutes. The resulting radiopharmaceutical is sterile and pyrogen-free and of a high chemical, radiochemical, and radionuclide purity proved by chromatographic techniques. The yield of the process is up to 20%. [(11)C]-choline PET scanning can be used as accurate and effective diagnostic tool in all centers equipped with [(11)C]-target containing cyclotron. PMID:27660552

  14. Synthesis, isolation and purification of [(11)C]-choline.

    PubMed

    Szydło, Marcin; Jadwiński, Michał; Chmura, Agnieszka; Gorczewski, Kamil; Sokół, Maria

    2016-01-01

    [(11)C]-choline is an effective PET tracer used for imaging of neoplastic lesions and metastases of the prostate cancer. However, its production can be a challenge for manufacturers, as it has not yet been described in Polish or European pharmacopoeia. In this study the technical aspects of [(11)C]-choline production are described and detailed process parameters are provided. The quality control procedures for releasing [(11)C]-choline as solutio iniectabilis are also presented. The purity and quality of the radiopharmaceutical obtained according to the proposed method were find to be high enough to safely administrate the radiopharmaceutical to patients. Application of an automated synthesizer makes it possible to carry out the entire process of [(11)C]-choline production, isolation and purification within 20 minutes. It is crucial to maintain all aspects of the process as short as possible, since the decay half-time of carbon-11 is 20.4 minutes. The resulting radiopharmaceutical is sterile and pyrogen-free and of a high chemical, radiochemical, and radionuclide purity proved by chromatographic techniques. The yield of the process is up to 20%. [(11)C]-choline PET scanning can be used as accurate and effective diagnostic tool in all centers equipped with [(11)C]-target containing cyclotron.

  15. Synthesis, isolation and purification of [11C]-choline

    PubMed Central

    Jadwiński, Michał; Chmura, Agnieszka; Gorczewski, Kamil; Sokół, Maria

    2016-01-01

    [11C]-choline is an effective PET tracer used for imaging of neoplastic lesions and metastases of the prostate cancer. However, its production can be a challenge for manufacturers, as it has not yet been described in Polish or European pharmacopoeia. In this study the technical aspects of [11C]-choline production are described and detailed process parameters are provided. The quality control procedures for releasing [11C]-choline as solutio iniectabilis are also presented. The purity and quality of the radiopharmaceutical obtained according to the proposed method were find to be high enough to safely administrate the radiopharmaceutical to patients. Application of an automated synthesizer makes it possible to carry out the entire process of [11C]-choline production, isolation and purification within 20 minutes. It is crucial to maintain all aspects of the process as short as possible, since the decay half-time of carbon-11 is 20.4 minutes. The resulting radiopharmaceutical is sterile and pyrogen-free and of a high chemical, radiochemical, and radionuclide purity proved by chromatographic techniques. The yield of the process is up to 20%. [11C]-choline PET scanning can be used as accurate and effective diagnostic tool in all centers equipped with [11C]-target containing cyclotron. PMID:27660552

  16. Carbon Cycling and Storage in Mangrove Forests

    NASA Astrophysics Data System (ADS)

    Alongi, Daniel M.

    2014-01-01

    Mangroves are ecologically and economically important forests of the tropics. They are highly productive ecosystems with rates of primary production equal to those of tropical humid evergreen forests and coral reefs. Although mangroves occupy only 0.5% of the global coastal area, they contribute 10-15% (24 Tg C y-1) to coastal sediment carbon storage and export 10-11% of the particulate terrestrial carbon to the ocean. Their disproportionate contribution to carbon sequestration is now perceived as a means for conservation and restoration and a way to help ameliorate greenhouse gas emissions. Of immediate concern are potential carbon losses to deforestation (90-970 Tg C y-1) that are greater than these ecosystems' rates of carbon storage. Large reservoirs of dissolved inorganic carbon in deep soils, pumped via subsurface pathways to adjacent waterways, are a large loss of carbon, at a potential rate up to 40% of annual primary production. Patterns of carbon allocation and rates of carbon flux in mangrove forests are nearly identical to those of other tropical forests.

  17. Carbon cycling and storage in mangrove forests.

    PubMed

    Alongi, Daniel M

    2014-01-01

    Mangroves are ecologically and economically important forests of the tropics. They are highly productive ecosystems with rates of primary production equal to those of tropical humid evergreen forests and coral reefs. Although mangroves occupy only 0.5% of the global coastal area, they contribute 10-15% (24 Tg C y(-1)) to coastal sediment carbon storage and export 10-11% of the particulate terrestrial carbon to the ocean. Their disproportionate contribution to carbon sequestration is now perceived as a means for conservation and restoration and a way to help ameliorate greenhouse gas emissions. Of immediate concern are potential carbon losses to deforestation (90-970 Tg C y(-1)) that are greater than these ecosystems' rates of carbon storage. Large reservoirs of dissolved inorganic carbon in deep soils, pumped via subsurface pathways to adjacent waterways, are a large loss of carbon, at a potential rate up to 40% of annual primary production. Patterns of carbon allocation and rates of carbon flux in mangrove forests are nearly identical to those of other tropical forests. PMID:24405426

  18. Carbon Nanomembranes.

    PubMed

    Turchanin, Andrey; Gölzhäuser, Armin

    2016-08-01

    Carbon nanomembranes (CNMs) are synthetic 2D carbon sheets with tailored physical or chemical properties. These depend on the structure, molecular composition, and surroundings on either side. Due to their molecular thickness, they can be regarded as "interfaces without bulk" separating regions of different gaseous, liquid, or solid components and controlling the materials exchange between them. Here, a universal scheme for the fabrication of 1 nm-thick, mechanically stable, functional CNMs is presented. CNMs can be further modified, for example perforated by ion bombardment or chemically functionalized by the binding of other molecules onto the surfaces. The underlying physical and chemical mechanisms are described, and examples are presented for the engineering of complex surface architectures, e.g., nanopatterns of proteins, fluorescent dyes, or polymer brushes. A simple transfer procedure allows CNMs to be placed on various support structures, which makes them available for diverse applications: supports for electron and X-ray microscopy, nanolithography, nanosieves, Janus nanomembranes, polymer carpets, complex layered structures, functionalization of graphene, novel nanoelectronic and nanomechanical devices. To close, the potential of CNMs in filtration and sensorics is discussed. Based on tests for the separation of gas molecules, it is argued that ballistic membranes may play a prominent role in future efforts of materials separation. PMID:27281234

  19. Pioneer 11's New Saturn.

    ERIC Educational Resources Information Center

    Science News, 1979

    1979-01-01

    New findings about the planet, Saturn and its environs, as collected by Pioneer 11 are detailed. Topics discussed include: the composition of the planet's interior, the search for new satellites, and the planet's magnetic field. (BT)

  20. Official Apollo 11 Crew Photo

    NASA Technical Reports Server (NTRS)

    1971-01-01

    The Official Crew Photo of the Apollo 11 Prime Crew. From left to right are Astronauts Neil A. Armstrong, Commander; Michael Collins, Command Module Pilot; and Edwin E. Aldrin Jr., Lunar Module Pilot.

  1. Trading forest carbon

    EPA Science Inventory

    The nature of carbon in forests is discussed from the perspective of carbon trading. Carbon inventories, specifically in the area of land use and forestry are reviewed for the Pacific Northwest. Carbon turnover in forests is discussed as it relates to carbon sequestration. Scient...

  2. Carbon Farming as a Carbon Negative Technology

    NASA Astrophysics Data System (ADS)

    Anderson, C.; Laird, D.; Hayes, D. J.

    2015-12-01

    Carbon farms have a pivotal role in national and international efforts to mitigate and adapt to climate change. A carbon farm in its broadest sense is one that reduces greenhouse gas (GHG) emissions or captures and holds carbon in vegetation and soils. Their capacity to remove carbon from the air and store it safely and permanently, while providing additional human and ecosystem benefits, means they could contribute significantly to national efforts to stabilize or reduce GHGs. We examine carbon farms in the context of corn and soybean production agriculture. We illustrate, using Iowa data but with relevance across United States corn and soybean production, the potential for carbon farms to reduce human GHG emissions and sequester carbon permanently at a rate that has meaningful impact on global greenhouse gas concentration. Carbon has been viewed as a next generation cash crop in Iowa for over a decade. The carbon farm perspective, however, goes beyond carbon as cash crop to make carbon the center of an entire farm enterprise. The transformation is possible through slight adjustment crop practices mixed with advances in technology to sequester carbon through biochar. We examine carbon balance of Iowa agriculture given only the combination of slight reduction in fertilizer and sequestration by biochar. We find the following. Iowa carbon farms could turn Iowa agriculture into a carbon sink. The estimated range of GHG reduction by statewide implementation of carbon farms is 19.46 to 90.27 MMt CO2-equivalent (CO2-e), while the current agricultural CO2-e emission estimate is 35.38 MMt CO2-e. Iowa carbon farm GHG reduction would exceed Iowa GHG reduction by wind energy (8.7 MMt CO2-e) and could exceed combined reductions from wind energy and corn grain ethanol (10.7 MMt CO2-e; 19.4 MMt CO2-e combined). In fact, Iowa carbon farms alone could exceed GHG reduction from national corn grain ethanol production (39.6 MMt CO2-e). A carbon price accessible to agricultural

  3. Carbon-Carbon Bond Cleavage in Activation of the Prodrug Nabumetone

    PubMed Central

    Varfaj, Fatbardha; Zulkifli, Siti N. A.; Park, Hyoung-Goo; Challinor, Victoria L.; De Voss, James J.

    2014-01-01

    Carbon-carbon bond cleavage reactions are catalyzed by, among others, lanosterol 14-demethylase (CYP51), cholesterol side-chain cleavage enzyme (CYP11), sterol 17β-lyase (CYP17), and aromatase (CYP19). Because of the high substrate specificities of these enzymes and the complex nature of their substrates, these reactions have been difficult to characterize. A CYP1A2-catalyzed carbon-carbon bond cleavage reaction is required for conversion of the prodrug nabumetone to its active form, 6-methoxy-2-naphthylacetic acid (6-MNA). Despite worldwide use of nabumetone as an anti-inflammatory agent, the mechanism of its carbon-carbon bond cleavage reaction remains obscure. With the help of authentic synthetic standards, we report here that the reaction involves 3-hydroxylation, carbon-carbon cleavage to the aldehyde, and oxidation of the aldehyde to the acid, all catalyzed by CYP1A2 or, less effectively, by other P450 enzymes. The data indicate that the carbon-carbon bond cleavage is mediated by the ferric peroxo anion rather than the ferryl species in the P450 catalytic cycle. CYP1A2 also catalyzes O-demethylation and alcohol to ketone transformations of nabumetone and its analogs. PMID:24584631

  4. Carbon dioxide concentrator

    NASA Technical Reports Server (NTRS)

    Williams, C. F.; Huebscher, R. G.

    1972-01-01

    Passed exhaled air through electrochemical cell containing alkali metal carbonate aqueous solution, and utilizes platinized electrodes causing reaction of oxygen at cathode with water in electrolyte, producing hydroxyl ions which react with carbon dioxide to form carbonate ions.

  5. 11. "TEST STANDS NOS. 11, 13, & 15; CONCRETE STRUCTURAL ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    11. "TEST STANDS NOS. 1-1, 1-3, & 1-5; CONCRETE STRUCTURAL SECTIONS AND DETAILS." Specifications No. OC12-50-10; Drawing No. 60-09-04; no sheet number within title block. D.O. SERIES 1109/15, Rev. E. Stamped: RECORD DRAWING - AS CONSTRUCTED. Below stamp: Contract DA-04353 Eng. 177, Rev. E; Date: 21 Dec. 1951. - Edwards Air Force Base, Air Force Rocket Propulsion Laboratory, Test Stand 1-5, Test Area 1-115, northwest end of Saturn Boulevard, Boron, Kern County, CA

  6. Salts of the 1-cyanocarba-closo-dodecaborate anions [1-NC-closo-1-CB11X11]- (X = H, F, Cl, Br, I).

    PubMed

    Finze, Maik; Sprenger, Jan A P; Schaack, Bernd Bastian

    2010-03-14

    The caesium and tetraethylammonium salts of the 1-cyanocarba-closo-dodecaborate anions [1-NC-closo-1-CB(11)X(11)](-) (X = H, F, Cl, Br, I) were synthesized from CsLi[closo-1-CB(11)X(11)] and phenylcyanate. All anions are stable against aqueous acids and bases, except for the fluorinated anion [1-NC-closo-1-CB(11)F(11)](-) that immediately reacts with water. The Cs(+) and [Et(4)N](+) salts of the anions were characterized by IR, Raman and multinuclear NMR spectroscopy as well as by MALDI and ESI mass spectrometry. The thermal properties of the Cs[1-NC-closo-1-CB(11)X(11)] (X = H, Cl, Br, I) and of some of their tetraethylammonium salts were studied by differential scanning calorimetry. The crystal structures of [Et(4)N][1-NC-closo-1-CB(11)H(11)] and Cs[1-NC-closo-1-CB(11)Cl(11)] were determined and the discussion of the structural and spectroscopic properties is supported by density functional and (RI)-MP2 calculations. A first insight into the hydrolysis of the [1-NC-closo-1-CB(11)F(11)](-) anion is presented and its reactions with water are compared to those of other undecafluorinated carba-closo-dodecaborate anions. The reduced hydrolytic stability of the [1-NC-closo-1-CB(11)F(11)](-) anion in comparison to its homologues is related to differences in the carbon-boron and boron-boron bond lengths of the {closo-1-CB(11)} cage and to different partial charges of the cluster atoms.

  7. Method of making carbon-carbon composites

    DOEpatents

    Engle, Glen B.

    1993-01-01

    A process for making 2D and 3D carbon-carbon composites having a combined high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizible woven cloth are infiltrated with carbon material to form green composites. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnant step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500.degree. to 3100.degree. C. to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000.degree. C. to 1300.degree. C. at a reduced. pressure.

  8. Exposure to fluorotrichloromethane (R-11).

    PubMed

    Angerer, J; Schröder, B; Heinrich, R

    1985-01-01

    Three volunteers were exposed to fluorotrichloromethane (R-11) under experimental conditions. Solvent levels in ambient and alveolar air, in blood and urine were measured. The mean concentration of R-11 in ambient air was 657 ml/m3. The average values of pulmonary retention and solvent levels in alveolar air and blood were 18.2%; 537 ml/m3 and 2.8 mg/l. Inter-individual variations of these parameters are negligible. R-11 concentrations in urine--in contrast to blood or alveolar air--depend on the dose taken up. After termination of exposure, R-11 concentrations in alveolar air and in blood are excreted with biological half-lives of seven and eleven minutes respectively during the first phase of elimination and with 1.8 and 1.0 h respectively during the second phase of elimination. Though ambient monitoring should, in most cases, be sufficient for the prevention of occupational diseases, the R-11 concentration in alveolar air seems to be the best parameter if biological monitoring seems to be necessary. PMID:4030118

  9. 40 CFR Table 11 to Subpart Uuu of... - Requirements for Performance Tests for Organic HAP Emissions From Catalytic Cracking Units Not...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ...) for Carbon Monoxide (CO) 11 Table 11 to Subpart UUU of Part 63 Protection of Environment ENVIRONMENTAL... Carbon Monoxide (CO) As stated in § 63.1565(b)(2) and (3), you shall meet each requirement in the... from all the readings. f. If you use a flare, conduct visible emission observations. Method 22 (40...

  10. 40 CFR Table 11 to Subpart Uuu of... - Requirements for Performance Tests for Organic HAP Emissions From Catalytic Cracking Units Not...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ...) for Carbon Monoxide (CO) 11 Table 11 to Subpart UUU of Part 63 Protection of Environment ENVIRONMENTAL... Carbon Monoxide (CO) As stated in § 63.1565(b)(2) and (3), you shall meet each requirement in the... from all the readings. f. If you use a flare, conduct visible emission observations. Method 22 (40...

  11. Carbon Capture (Carbon Cycle 2.0)

    ScienceCinema

    Smit, Berend

    2016-07-12

    Berend Smit speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 3, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/

  12. Integral Ring Carbon-Carbon Piston

    NASA Technical Reports Server (NTRS)

    Northam, G. Burton (Inventor)

    1999-01-01

    An improved structure for a reciprocating internal combustion engine or compressor piston fabricate from carbon-carbon composite materials is disclosed. An integral ring carbon-carbon composite piston, disclosed herein, reduces the need for piston rings and for small clearances by providing a small flexible, integral component around the piston that allows for variation in clearance due to manufacturing tolerances, distortion due to pressure and thermal loads, and variations in thermal expansion differences between the piston and cylinder liner.

  13. PWC-11 fuel pin development for SP-100

    NASA Astrophysics Data System (ADS)

    Sayre, Edwin D.; Butler, Robert E.; Kangilaski, Mike

    1992-01-01

    GE has developed a high temperature fuel pin for the SP-100 Space Reactor. The Nb-1% Zr alloy PWC-11 was selected over the conventional Nb-1% Ar alloy for the fuel pin cladding because the higher creep strength enables a significant reduction in system mass. PWC-11 has 0.1% carbon to provide the higher creep and tensile strength at the operating temperature. PWC-11 was developed by Pratt and Whitney in the 1960's and it has also been investigated by the Russians. Six small 35 pound ingots were purchased from Teledyne Wah Chang, five by Nasa Lewis Research Center, and one by GE for the SP-100. Since no work had been done during the last two decades, processes had to be developed based on the work done earlier. The tube making process experience at GE is discussed.

  14. 48 CFR 6101.11 - Conferences; conference memorandum [Rule 11].

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... agreements disposing of matters in dispute; or (6) Ways to expedite disposition of the case or to facilitate settlement of the dispute, including, if the parties and the Board agree, the use of alternative dispute... APPEALS, GENERAL SERVICES ADMINISTRATION CONTRACT DISPUTE CASES 6101.11 Conferences; conference...

  15. 48 CFR 6101.11 - Conferences; conference memorandum [Rule 11].

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... agreements disposing of matters in dispute; or (6) Ways to expedite disposition of the case or to facilitate settlement of the dispute, including, if the parties and the Board agree, the use of alternative dispute... APPEALS, GENERAL SERVICES ADMINISTRATION CONTRACT DISPUTE CASES 6101.11 Conferences; conference...

  16. Carbon Residence Times in Pedogenic Carbonate Pools

    NASA Astrophysics Data System (ADS)

    Monger, H.; Feng, Y.; Karnjanapiboonwang, A.

    2013-12-01

    Soil carbonate is a huge pool of terrestrial carbon that contains at least 930 to 940 Pg C and has influx rates on the order of 1 to 12 g CaCO3/m2/yr. Such large mass to flux ratios yield long mean residence times for carbon (e.g., 85,000 years)--assuming steady state. Like other global carbon pools, the soil carbonate pool has smaller sub-pools with higher influx rates and shorter mean residence times. For example, pedogenic carbonate in coppice dunes known to have formed since 1858 and carbonate formed on lithic artifacts in soils at archaeology sites suggests mean residence times can be as short as 120 years--again assuming steady state. Harder to assess are efflux rates as CO2 emissions or bicarbonate leaching. Some Bowen-ratio studies have nevertheless found evidence for CO2 emissions resulting from carbonate dissolution, and other studies have found evidence for bicarbonate leaching based on dissolution pipes through calcic horizons using soil morphology studies. Since an understanding of mean residence times are prerequisite for a better understanding of soil carbonate in the global carbon cycle, especially in a scenario of an expanding Aridosphere, more influx and efflux measurements are needed to evaluate the possibility of carbon sequestration by soil carbonate in hyperarid, arid, semiarid, or subhumid soils.

  17. Composite carbon foam electrode

    DOEpatents

    Mayer, S.T.; Pekala, R.W.; Kaschmitter, J.L.

    1997-05-06

    Carbon aerogels used as a binder for granulated materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivity and power to system energy. 1 fig.

  18. Composite carbon foam electrode

    DOEpatents

    Mayer, Steven T.; Pekala, Richard W.; Kaschmitter, James L.

    1997-01-01

    Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivty and power to system energy.

  19. Variable Carbon Isotopes in ALH84001 Carbonates

    NASA Astrophysics Data System (ADS)

    Niles, P. B.; Leshin, L. A.; Guan, Y.

    2002-12-01

    The Martian meteorite ALH84001 contains a small amount of carbonate that was deposited from aqueous fluids on the Martian surface approximately 3.9 Ga.. McKay et al. (1996) proposed evidence for the existence of life preserved within the carbonate grains. In order to determine the nature of the ancient Martian aqueous system we have combined previously collected oxygen isotopic data with new carbon isotopic measurements performed on the Cameca 6f ion microprobe at Arizona State University. Isotopic measurements were made at high mass resolution with a spot size of 10 microns. The measured carbon isotopic values range from 29.2‰ to 64.5‰ (PDB) with an average uncertainty of +/-1.6‰ (1σ ). These data agree very well with previous acid dissolution and stepped combustion experiments which range from a δ13C of +32‰ to +41‰ . As observed with the oxygen isotopic data, the carbon isotopic composition is correlated with the chemical composition of the carbonates. This allows us to establish that the earliest (Ca-rich) carbonates had the lightest carbon isotopic composition while the latest forming (Mg-rich) carbonates had the heaviest carbon isotopic composition. The large range of carbon isotopic compositions measured in this study cannot be explained by previously proposed models. Temperature change or a Rayleigh distillation process caused by progressive carbonate precipitation are insufficient to create the observed carbon isotopic compositions. Furthermore, processes such as evaporation or photosynthesis will not produce large carbon isotopic variations due to rapid isotopic equilibration with the atmosphere. We propose two possible models for the formation of the ALH84001 carbonates consistent with the isotopic data collected thus far. Carbonates could have formed from an evolving system where the carbon and oxygen isotopic composition of the carbonates reflects a mixing between magmatic hydrothermal fluids and fluids in equilibrium with an isotopically

  20. Deep Soil Carbon: The Insight into Global Carbon Estimation and Deforestation Impacts

    NASA Astrophysics Data System (ADS)

    Sangmanee, Podjanee; Dell, Bernard; Harper, Richard; Henry, David

    2015-04-01

    World carbon stocks have been dramatically changed by deforestation. The current estimation of carbon loss is based on allometric techniques assisted with satellite imagery and the assumption that, 20% of the total biomass carbon stock is below ground. However, the monitoring of soil carbon is limited to 0.3 m despite many soils being much deeper than this. For example, direct measurement of soil carbon demonstrated the occurrence of two to five times more carbon stored in deep soils of south Western Australia (SWA) compared to what would normally be reported, although the land had been deforested for 80 years. This raises important questions about the dynamics of this deeper carbon and whether it will contribute to global climate change. This paper reports the form and variation of carbon in soil at three adjacent areas at three different depths (0-1, 11-12 and 18-19 m). Techniques were developed to quantitatively and qualitatively determine small concentrations of carbon in deep soils. There were marked differences in carbon compounds with depth. Near the surface these were macromolecular organic compounds derived from lignin, polysaccharides, proteins, terpenes, whereas at depth they were low molecular weight compounds, 13-docosenamide, 13-docosenoate, xanthone, benzophenone. The deeper compounds are likely derived from the roots of the previous forest whereas the surface soils are affected by current land use. The in situ decomposition of deep roots was revealed by the pyridine compound. The variation of compounds and location of carbon in clay could imply the state of decomposition. The result demonstrated that carbon is contained in deep soils and should be considered in global carbon accounting, particularly given ongoing deforestation on deep soils.

  1. From carbon nanotubes to carbon atomic chains

    NASA Astrophysics Data System (ADS)

    Casillas García, Gilberto; Zhang, Weijia; José-Yacamán, Miguel

    2010-10-01

    Carbyne is a linear allotrope of carbon. It is formed by a linear arrangement of carbon atoms with sp-hybridization. We present a reliable and reproducible experiment to obtain these carbon atomic chains using few-layer-graphene (FLG) sheets and a HRTEM. First the FLG sheets were synthesized from worm-like exfoliated graphite and then drop-casted on a lacey-carbon copper grid. Once in the TEM, two holes are opened near each other in a FLG sheet by focusing the electron beam into a small spot. Due to the radiation, the carbon atoms rearrange themselves between the two holes and form carbon fibers. The beam is concentrated on the carbon fibers in order excite the atoms and induce a tension until multi wall carbon nanotube (MWCNT) is formed. As the radiation continues the MWCNT breaks down until there is only a single wall carbon nanotube (SWCNT). Then, when the SWCNT breaks, an atomic carbon chain is formed, lasts for several seconds under the radiation and finally breaks. This demonstrates the stability of this carbon structure.

  2. Pioneer 11 Encounter. [with Jupiter

    NASA Technical Reports Server (NTRS)

    1975-01-01

    Pioneer 11's encounter with Jupiter is discussed in detail. The scientific experiments carried out on the probe are described along with the instruments used. Tables are included which provide data on the times of experiments, encounters, and the distances from Jupiter. Educational study projects are also given.

  3. Earth Science 11. Curriculum Guide.

    ERIC Educational Resources Information Center

    British Columbia Dept. of Education, Victoria.

    This publication, developed by the Ministry of Education, Province of British Columbia, Canada, is a teaching guide for the Earth Science 11 course. The course is intended to provide secondary school students with the background and desire to investigate their earth, its materials and its processes. The guide consists of four sections. Section A…

  4. Apollo 11 Lunar Science Conference

    ERIC Educational Resources Information Center

    Cochran, Wendell

    1970-01-01

    Report of a conference called to discuss the findings of 142 scientists from their investigations of samples of lunar rock and soil brought back by the Apollo 11 mission. Significant findings reported include the age and composition of the lunar samples, and the absence of water and organic matter. Much discussed was the origin and structure of…

  5. Activity Book. Celebrate Apollo 11.

    ERIC Educational Resources Information Center

    Barchert, Linda; And Others

    1994-01-01

    An activity book helps students learn about the 1969 Apollo 11 mission to the moon as they get a sense of the mission's impact on their lives. The activities enhance understanding of science, math, social studies, and language arts. A teacher's page offers information on books, magazines, computer materials, and special resources. (SM)

  6. Sociology. Grades 11 & 12. Revised.

    ERIC Educational Resources Information Center

    Hamilton Township Schools, NJ.

    This curriculum guide presents both general information on K-12 social studies curriculum development and information specific to designing an 11th and 12th grade sociology curriculum. A foreword and preface describe Hamilton Township's (New Jersey) K-12 social studies program sequence, curriculum and instruction design criteria, and support…

  7. Carbon in, Carbon out: Reevaluating Carbon Fluxes in Subduction Zones

    NASA Astrophysics Data System (ADS)

    Manning, C. E.; Kelemen, P. B.

    2015-12-01

    Subduction zones exert a fundamental control on the deep carbon cycle. We reevaluated carbon inputs and outputs in convergent margins considering new estimates of C concentration in subducting mantle peridotites, carbonate solubility in aqueous fluids along subduction geotherms, melting and diapirism of carbon-bearing metasediments, and diffuse degassing from arcs. Our updated estimate of carbon inputs to the global subduction system, which includes estimates for C in altered peridotite, is 40-66 megatons carbon/year (MtC/y). We find that estimates of C lost from slabs (14-66 MtC/y) must take into account the high CaCO3 solubility in aqueous fluids, which contributes significant C that must be added to that derived from mineral decarbonation reactions. When taken together with hydrous silicate and carbonatite melts and metasediment diapirs, nearly all C can be scavenged from subducting lithosphere. The return of C to the atmosphere via arc-volcano degassing is only 18-43 MtC/y, but consideration deep volatile saturation of arc magmas, magma ponding in the middle and deep arc crust, and CO2 venting in forearcs can account for the remaining C lost from the slab. Thus, whereas previous studies concluded that about half the subducting carbon is returned to the convecting mantle, we find that relatively little carbon may be recycled. If so, substantial quantities of carbon are stored in the mantle lithosphere and crust and the carbon content of the mantle lithosphere + crust + ocean + atmosphere must be increasing, at least over the last 5-10 My. This is consistent with inferences from noble gas data. Recycled carbon in diamonds is a small fraction of the global carbon inventory.

  8. Analysis of Carbon Nanotube Field-Effect-Transistors (FETs)

    NASA Technical Reports Server (NTRS)

    Yamada, Toshishige

    1999-01-01

    This five page presentation is grouped into 11 numbered viewgraphs, most of which contain one or more diagrams. Some of the diagrams are accompanied by captions, including: 2) Nanotube FET by Delft, IBM; 3) Nanotube FET/Standard MOSFET; 5) Saturation with carrier-carrier; 7) Electronic properties of carbon nanotube; 8) Theoretical nanotube FET characteristics; 11) Summary: Delft and IBM nanotube FET analysis.

  9. 40 CFR 63.990 - Absorbers, condensers, and carbon adsorbers used as control devices.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... regeneration cycle; and a carbon bed temperature monitoring device, capable of recording the carbon bed... 40 Protection of Environment 11 2013-07-01 2013-07-01 false Absorbers, condensers, and carbon..., Recovery Devices and Routing to a Fuel Gas System or a Process § 63.990 Absorbers, condensers, and...

  10. 40 CFR 63.990 - Absorbers, condensers, and carbon adsorbers used as control devices.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... regeneration cycle; and a carbon bed temperature monitoring device, capable of recording the carbon bed... 40 Protection of Environment 11 2012-07-01 2012-07-01 false Absorbers, condensers, and carbon..., Recovery Devices and Routing to a Fuel Gas System or a Process § 63.990 Absorbers, condensers, and...

  11. 10 CFR 11.7 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... COMMISSION CRITERIA AND PROCEDURES FOR DETERMINING ELIGIBILITY FOR ACCESS TO OR CONTROL OVER SPECIAL NUCLEAR... job falling within the criterion of § 11.11(a)(2). NRC-“U” special nuclear material access... to work at a job falling within the criterion of 11.11(a)(1) or 11.13. Special nuclear...

  12. 7 CFR 1735.11 - Area coverage.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... effect this requirement. See 7 CFR 1737.11(a), Preapplication Determinations: Area to be Served. ... 7 Agriculture 11 2014-01-01 2014-01-01 false Area coverage. 1735.11 Section 1735.11 Agriculture... Policies § 1735.11 Area coverage. Borrowers must make adequate telephone service available to the...

  13. 7 CFR 1735.11 - Area coverage.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... effect this requirement. See 7 CFR 1737.11(a), Preapplication Determinations: Area to be Served. ... 7 Agriculture 11 2010-01-01 2010-01-01 false Area coverage. 1735.11 Section 1735.11 Agriculture... Policies § 1735.11 Area coverage. Borrowers must make adequate telephone service available to the...

  14. 7 CFR 1735.11 - Area coverage.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... effect this requirement. See 7 CFR 1737.11(a), Preapplication Determinations: Area to be Served. ... 7 Agriculture 11 2013-01-01 2013-01-01 false Area coverage. 1735.11 Section 1735.11 Agriculture... Policies § 1735.11 Area coverage. Borrowers must make adequate telephone service available to the...

  15. 7 CFR 1735.11 - Area coverage.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... effect this requirement. See 7 CFR 1737.11(a), Preapplication Determinations: Area to be Served. ... 7 Agriculture 11 2011-01-01 2011-01-01 false Area coverage. 1735.11 Section 1735.11 Agriculture... Policies § 1735.11 Area coverage. Borrowers must make adequate telephone service available to the...

  16. 7 CFR 1735.11 - Area coverage.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... effect this requirement. See 7 CFR 1737.11(a), Preapplication Determinations: Area to be Served. ... 7 Agriculture 11 2012-01-01 2012-01-01 false Area coverage. 1735.11 Section 1735.11 Agriculture... Policies § 1735.11 Area coverage. Borrowers must make adequate telephone service available to the...

  17. 11 CFR 300.30 - Accounts.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... demonstrate through a reasonable accounting method approved by the Commission (including any method embedded... party, whether or not the committee is a political committee under 11 CFR 100.5, that have receipts or..., 11 CFR 102.5(a)(4), 11 CFR 106.7(d)(1)(i), 11 CFR 300.33 and 11 CFR 300.34. (2) Levin account....

  18. Carbon nanotube composite materials

    DOEpatents

    O'Bryan, Gregory; Skinner, Jack L; Vance, Andrew; Yang, Elaine Lai; Zifer, Thomas

    2015-03-24

    A material consisting essentially of a vinyl thermoplastic polymer, un-functionalized carbon nanotubes and hydroxylated carbon nanotubes dissolved in a solvent. Un-functionalized carbon nanotube concentrations up to 30 wt % and hydroxylated carbon nanotube concentrations up to 40 wt % can be used with even small concentrations of each (less than 2 wt %) useful in producing enhanced conductivity properties of formed thin films.

  19. Acetylenic carbon allotrope

    DOEpatents

    Lagow, Richard J.

    1998-01-01

    A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein.

  20. Acetylenic carbon allotrope

    DOEpatents

    Lagow, Richard J.

    1999-01-01

    A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein.

  1. Acetylenic carbon allotrope

    DOEpatents

    Lagow, R.J.

    1998-02-10

    A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein. 17 figs.

  2. Pyrolyzed thin film carbon

    NASA Technical Reports Server (NTRS)

    Tai, Yu-Chong (Inventor); Liger, Matthieu (Inventor); Harder, Theodore (Inventor); Konishi, Satoshi (Inventor); Miserendino, Scott (Inventor)

    2010-01-01

    A method of making carbon thin films comprises depositing a catalyst on a substrate, depositing a hydrocarbon in contact with the catalyst and pyrolyzing the hydrocarbon. A method of controlling a carbon thin film density comprises etching a cavity into a substrate, depositing a hydrocarbon into the cavity, and pyrolyzing the hydrocarbon while in the cavity to form a carbon thin film. Controlling a carbon thin film density is achieved by changing the volume of the cavity. Methods of making carbon containing patterned structures are also provided. Carbon thin films and carbon containing patterned structures can be used in NEMS, MEMS, liquid chromatography, and sensor devices.

  3. Mesoporous carbon materials

    DOEpatents

    Dai, Sheng; Fulvio, Pasquale Fernando; Mayes, Richard T.; Wang, Xiqing; Sun, Xiao-Guang; Guo, Bingkun

    2014-09-09

    A conductive mesoporous carbon composite comprising conductive carbon nanoparticles contained within a mesoporous carbon matrix, wherein the conductive mesoporous carbon composite possesses at least a portion of mesopores having a pore size of at least 10 nm and up to 50 nm, and wherein the mesopores are either within the mesoporous carbon matrix, or are spacings delineated by surfaces of said conductive carbon nanoparticles when said conductive carbon nanoparticles are fused with each other, or both. Methods for producing the above-described composite, devices incorporating them (e.g., lithium batteries), and methods of using them, are also described.

  4. Carbon distribution profiles in lunar fines

    NASA Technical Reports Server (NTRS)

    Hart, R. K.

    1977-01-01

    Radial distribution profiles of elemental carbon in lunar soils consisting of particles in the size range of 50 to 150 microns were investigated. Initial experiments on specimen preparation and the analysis of prepared specimens by Auger electron spectrometry (AES) and scanning electron microscopy (SEM) are described. Results from splits of samples 61501,84 and 64421,11, which were mounted various ways in several specimen holders, are presented. A low carbon content was observed in AES spectra from soil particles that were subjected to sputter-ion cleaning with 960eV argon ions for periods of time up to a total exposure for one hour. This ion charge was sufficient to remove approximately 70 nm of material from the surface. All of the physically adsorbed carbon (as well as water vapor, etc.) would normally be removed in the first few minutes, leaving only carbon in the specimen, and metal support structure, to be detected thereafter.

  5. Carbon isotopic fractionation in heterotrophic microbial metabolism

    NASA Technical Reports Server (NTRS)

    Blair, N.; Leu, A.; Munoz, E.; Olsen, J.; Kwong, E.; Des Marais, D.

    1985-01-01

    Differences in the natural-abundance carbon stable isotopic compositions between products from aerobic cultures of Escherichia coli K-12 were measured. Respired CO2 was 3.4 percent depleted in C-13 relative to the glucose used as the carbon source, whereas the acetate was 12.3 percent enriched in C-13. The acetate C-13 enrichment was solely in the carboxyl group. Even though the total cellular carbon was only 0.6 percent depleted in C-13, intracellular components exhibited a significant isotopic heterogeneity. The protein and lipid fractions were -1.1 and -2.7 percent, respectively. Aspartic and glutamic acids were -1.6 and +2.7 percent, respectively, yet citrate was isotopically identical to the glucose. Probable sites of carbon isotopic fractionation include the enzyme, phosphotransacetylase, and the Krebs cycle.

  6. Carbon isotopic fractionation in heterotrophic microbial metabolism

    SciTech Connect

    Blair, N.; Leu, A.; Munoz, E.; Olsen, J.; Kwong, E.; Des Marais, D.

    1985-10-01

    Differences in the natural-abundance carbon stable isotopic compositions between products from aerobic cultures of Escherichia coli K-12 were measured. Respired CO2 was 3.4 percent depleted in C-13 relative to the glucose used as the carbon source, whereas the acetate was 12.3 percent enriched in C-13. The acetate C-13 enrichment was solely in the carboxyl group. Even though the total cellular carbon was only 0.6 percent depleted in C-13, intracellular components exhibited a significant isotopic heterogeneity. The protein and lipid fractions were -1.1 and -2.7 percent, respectively. Aspartic and glutamic acids were -1.6 and +2.7 percent, respectively, yet citrate was isotopically identical to the glucose. Probable sites of carbon isotopic fractionation include the enzyme, phosphotransacetylase, and the Krebs cycle. 38 references.

  7. 17 CFR 240.11a1-1(T) - Transactions yielding priority, parity, and precedence.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... section 11(a)(1) of the Act or specified in 17 CFR 240.11a1-4(T) shall be deemed to be revenue derived..., parity, and precedence. 240.11a1-1(T) Section 240.11a1-1(T) Commodity and Securities Exchanges SECURITIES... (rule 11a-1) § 240.11a1-1(T) Transactions yielding priority, parity, and precedence. (a) A...

  8. 17 CFR 240.11a1-1(T) - Transactions yielding priority, parity, and precedence.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... section 11(a)(1) of the Act or specified in 17 CFR 240.11a1-4(T) shall be deemed to be revenue derived..., parity, and precedence. 240.11a1-1(T) Section 240.11a1-1(T) Commodity and Securities Exchanges SECURITIES... (rule 11a-1) § 240.11a1-1(T) Transactions yielding priority, parity, and precedence. (a) A...

  9. 17 CFR 240.11a1-1(T) - Transactions yielding priority, parity, and precedence.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... section 11(a)(1) of the Act or specified in 17 CFR 240.11a1-4(T) shall be deemed to be revenue derived..., parity, and precedence. 240.11a1-1(T) Section 240.11a1-1(T) Commodity and Securities Exchanges SECURITIES... (rule 11a-1) § 240.11a1-1(T) Transactions yielding priority, parity, and precedence. (a) A...

  10. 17 CFR 240.11a1-1(T) - Transactions yielding priority, parity, and precedence.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... section 11(a)(1) of the Act or specified in 17 CFR 240.11a1-4(T) shall be deemed to be revenue derived..., parity, and precedence. 240.11a1-1(T) Section 240.11a1-1(T) Commodity and Securities Exchanges SECURITIES... (rule 11a-1) § 240.11a1-1(T) Transactions yielding priority, parity, and precedence. (a) A...

  11. 17 CFR 240.11a1-1(T) - Transactions yielding priority, parity, and precedence.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... section 11(a)(1) of the Act or specified in 17 CFR 240.11a1-4(T) shall be deemed to be revenue derived..., parity, and precedence. 240.11a1-1(T) Section 240.11a1-1(T) Commodity and Securities Exchanges SECURITIES... (rule 11a-1) § 240.11a1-1(T) Transactions yielding priority, parity, and precedence. (a) A...

  12. 43 CFR 11.19 - [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false 11.19 Section 11.19 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.19...

  13. 43 CFR 11.19 - [Reserved

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false 11.19 Section 11.19 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.19...

  14. 43 CFR 11.16 - [Reserved

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 43 Public Lands: Interior 1 2010-10-01 2010-10-01 false 11.16 Section 11.16 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.16...

  15. 43 CFR 11.16 - [Reserved

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 43 Public Lands: Interior 1 2011-10-01 2011-10-01 false 11.16 Section 11.16 Public Lands: Interior Office of the Secretary of the Interior NATURAL RESOURCE DAMAGE ASSESSMENTS Introduction § 11.16...

  16. Reduced Martian Carbon: Evidence from Martian Meteorites

    NASA Technical Reports Server (NTRS)

    Gibson, Everett K.; McKay, David S.; Thomas-Keprta, Kathie L.; Clemett, SImon J.; Pillinger, COlin T.; Wright, Ian P.; Verchovsky, A. P.

    2010-01-01

    Identification of indigenous reduced carbon species on Mars has been a challenge since the first hypotheses about life on Mars were proposed. Ranging from the early astronomical measurements to analyses of samples from the Martian surface in the form of Martian meteorites. The first direct attempt to analyze the carbon species on the surface was in 1976 with the Viking GC-MS in-situ experiment which gave inconclusive results at two sites on Mars [1]. With the recognition in 1983 that samples of the Martian surface were already present on Earth in the form of Martian meteorites by Bogard and Johnson [2] new opportunities became available for direct study of Mars's samples in te rlraesbtrioalratories. Carbon isotopic compositional information suggested a reduced carbon component was present in the Martian meteorites [3-5]. Polycyclic aromatic hydrocarbons associated with carbonate globules in ALH84001 were later identified [6,7]. Jull et al [8] noted that an insoluble component was present within Nakhla and more than 75% of its C lacked any 14C, which is modern-day carbon contaminant. This carbon fraction was believed to be either indigenous (i..e. Martian) or ancient meteoritic carbon phase. Within the fractures of Nakhla and ALH84001, Fisk et al [9,10] identified reduced carbon-enriched areas. Gibson et al. [11] using a combination of NanoSIMS, Focused Electron microscopy, Laser Raman Spectroscopy and Stepped-Combustion Static Mass Spectrometry analyses the presence of possible indigenous reduced carbon components within the 1.3 Ga old Nakhla.

  17. Rotational Bands in 11B

    NASA Astrophysics Data System (ADS)

    Demyanova, A. S.; Danilov, A. N.; Dmitriev, S. V.; Ogloblin, A. A.; Belyaeva, T. L.; Goncharov, S. A.; Gurov, Yu. B.; Maslov, V. A.; Sobolev, Yu. G.; Trzaska, W.; Heikkinen, P.; Julin, R.; Khlebnikov, S. V.; Tyurin, G. P.; Burtebaev, N.; Zholdybayev, T.

    2015-06-01

    Differential cross-sections of the 11B + α inelastic scattering at E(α) = 65 leading to the most of the known 11B states at the excitation energies up to 14 MeV were measured. The data analysis was done by DWBA and in some cases by the modified diffraction model allowing determining the radii of the excited states. The radii of the states with excitation energies less than ~ 7 MeV with the accuracy not less than 0.1-0.15 fm coincide with the radius of the ground state. This result is consistent with the traditional view of the shell structure of the low-lying states in 11B. Most of the observed high-energy excited states are distributed among four rotational bands. The moments of inertia of band states are close to the moment of inertia of the Hoyle state of 12C. The calculated radii, related to these bands, are 0.7 - 1.0 fm larger than the radius of the ground state, and are close to the radius of the Hoyle state. These results are in agreement with existing predictions about various cluster structure of 11B at high excitation energies. The state with the excitation energy 12.56 MeV, Iπ = 1/2+, T = 1/2 and the root mean square radius R ~ 6 fm predicted in the frame of the alpha condensate hypothesis was not found. The observed level at 12.6 MeV really has T = 1/2, probably, Iπ = 3/2+ and the radius close to that of the ground state.

  18. Apollo 11 preflight press conference

    NASA Technical Reports Server (NTRS)

    1969-01-01

    The three prime crewmen of the Apollo 11 lunar landing mission participate in a pre-flight press conference in the bldg 1 auditorium on July 5, 1969. Left to right, are Astronauts Neil A. Armstrong, commander; Edwin E. Aldrin Jr., lunar module pilot; and Michael Collins, command module pilot. The box-like enclosure surrounding the three astronauts was part of elaborate precautions in effect to reduce the possibility of exposing the crewmen to infectious disease in the preflight period.

  19. 11 CFR 300.30 - Accounts.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ..., 11 CFR 102.5(a)(4), 11 CFR 106.7(d)(1)(i), 11 CFR 300.33 and 11 CFR 300.34. (2) Levin account. The funds deposited into this account must comply with 11 CFR 300.31. Such funds may be used for the categories of activities described at 11 CFR 300.32(b). (3) Federal account. Federal accounts may be used...

  20. 11 CFR 300.30 - Accounts.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ..., 11 CFR 102.5(a)(4), 11 CFR 106.7(d)(1)(i), 11 CFR 300.33 and 11 CFR 300.34. (2) Levin account. The funds deposited into this account must comply with 11 CFR 300.31. Such funds may be used for the categories of activities described at 11 CFR 300.32(b). (3) Federal account. Federal accounts may be used...

  1. 11 CFR 300.30 - Accounts.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ..., 11 CFR 102.5(a)(4), 11 CFR 106.7(d)(1)(i), 11 CFR 300.33 and 11 CFR 300.34. (2) Levin account. The funds deposited into this account must comply with 11 CFR 300.31. Such funds may be used for the categories of activities described at 11 CFR 300.32(b). (3) Federal account. Federal accounts may be used...

  2. 11 CFR 300.30 - Accounts.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ..., 11 CFR 102.5(a)(4), 11 CFR 106.7(d)(1)(i), 11 CFR 300.33 and 11 CFR 300.34. (2) Levin account. The funds deposited into this account must comply with 11 CFR 300.31. Such funds may be used for the categories of activities described at 11 CFR 300.32(b). (3) Federal account. Federal accounts may be used...

  3. New Carbonate Standard Reference Materials for Boron Isotope Geochemistry

    NASA Astrophysics Data System (ADS)

    Stewart, J.; Christopher, S. J.; Day, R. D.

    2015-12-01

    The isotopic composition of boron (δ11B) in marine carbonates is well established as a proxy for past ocean pH. Yet, before palaeoceanographic interpretation can be made, rigorous assessment of analytical uncertainty of δ11B data is required; particularly in light of recent interlaboratory comparison studies that reported significant measurement disagreement between laboratories [1]. Well characterised boron standard reference materials (SRMs) in a carbonate matrix are needed to assess the accuracy and precision of carbonate δ11B measurements throughout the entire procedural chemistry; from sample cleaning, to ionic separation of boron from the carbonate matrix, and final δ11B measurement by multi-collector inductively coupled plasma mass spectrometry. To date only two carbonate reference materials exist that have been value-assigned by the boron isotope measurement community [2]; JCp-1 (porites coral) and JCt-1 (Giant Clam) [3]. The National Institute of Standards and Technology (NIST) will supplement these existing standards with new solution based inorganic carbonate boron SRMs that replicate typical foraminiferal and coral B/Ca ratios and δ11B values. These new SRMs will not only ensure quality control of full procedural chemistry between laboratories, but have the added benefits of being both in abundant supply and free from any restrictions associated with shipment of biogenic samples derived from protected species. Here we present in-house δ11B measurements of these new boron carbonate SRM solutions. These preliminary data will feed into an interlaboratory comparison study to establish certified values for these new NIST SRMs. 1. Foster, G.L., et al., Chemical Geology, 2013. 358(0): p. 1-14. 2. Gutjahr, M., et al., Boron Isotope Intercomparison Project (BIIP): Development of a new carbonate standard for stable isotopic analyses. Geophysical Research Abstracts, EGU General Assembly 2014, 2014. 16(EGU2014-5028-1). 3. Inoue, M., et al., Geostandards and

  4. CO2 capture in different carbon materials.

    PubMed

    Jiménez, Vicente; Ramírez-Lucas, Ana; Díaz, José Antonio; Sánchez, Paula; Romero, Amaya

    2012-07-01

    In this work, the CO(2) capture capacity of different types of carbon nanofibers (platelet, fishbone, and ribbon) and amorphous carbon have been measured at 26 °C as at different pressures. The results showed that the more graphitic carbon materials adsorbed less CO(2) than more amorphous materials. Then, the aim was to improve the CO(2) adsorption capacity of the carbon materials by increasing the porosity during the chemical activation process. After chemical activation process, the amorphous carbon and platelet CNFs increased the CO(2) adsorption capacity 1.6 times, whereas fishbone and ribbon CNFs increased their CO(2) adsorption capacity 1.1 and 8.2 times, respectively. This increase of CO(2) adsorption capacity after chemical activation was due to an increase of BET surface area and pore volume in all carbon materials. Finally, the CO(2) adsorption isotherms showed that activated amorphous carbon exhibited the best CO(2) capture capacity with 72.0 wt % of CO(2) at 26 °C and 8 bar.

  5. Global Carbon Budget 2015

    DOE PAGES

    Le Quéré, C.; Moriarty, R.; Andrew, R. M.; Canadell, J. G.; Sitch, S.; Korsbakken, J. I.; Friedlingstein, P.; Peters, G. P.; Andres, R. J.; Boden, T. A.; et al

    2015-12-07

    component of the global carbon budget. For the last decade available (2005–2014), EFF was 9.0 ± 0.5 GtC yr-1, ELUC was 0.9 ± 0.5 GtC yr-1, GATM was 4.4 ± 0.1 GtC yr-1, SOCEAN was 2.6 ± 0.5 GtC yr-1, and SLAND was 3.0 ± 0.8 GtC yr-1. For the year 2014 alone, EFF grew to 9.8 ± 0.5 GtC yr-1, 0.6 % above 2013, continuing the growth trend in these emissions, albeit at a slower rate compared to the average growth of 2.2 % yr-1 that took place during 2005–2014. Also, for 2014, ELUC was 1.1 ± 0.5 GtC yr-1, GATM was 3.9 ± 0.2 GtC yr-1, SOCEAN was 2.9 ± 0.5 GtC yr-1, and SLAND was 4.1 ± 0.9 GtC yr-1. GATM was lower in 2014 compared to the past decade (2005–2014), reflecting a larger SLAND for that year. The global atmospheric CO2 concentration reached 397.15 ± 0.10 ppm averaged over 2014. For 2015, preliminary data indicate that the growth in EFF will be near or slightly below zero, with a projection of -0.6 [range of -1.6 to +0.5] %, based on national emissions projections for China and the USA, and projections of gross domestic product corrected for recent changes in the carbon intensity of the global economy for the rest of the world. From this projection of EFF and assumed constant ELUC for 2015, cumulative emissions of CO2 will reach about 555 ± 55 GtC (2035 ± 205 GtCO2) for 1870–2015, about 75 % from EFF and 25 % from ELUC. Finally, this living data update documents changes in the methods and data sets used in this new carbon budget compared with previous publications of this data set (Le Quéré et al., 2015, 2014, 2013). All observations presented here can be downloaded from the Carbon Dioxide Information Analysis Center (doi:10.3334/CDIAC/GCP_2015).« less

  6. Global Carbon Budget 2015

    NASA Astrophysics Data System (ADS)

    Le Quéré, C.; Moriarty, R.; Andrew, R. M.; Canadell, J. G.; Sitch, S.; Korsbakken, J. I.; Friedlingstein, P.; Peters, G. P.; Andres, R. J.; Boden, T. A.; Houghton, R. A.; House, J. I.; Keeling, R. F.; Tans, P.; Arneth, A.; Bakker, D. C. E.; Barbero, L.; Bopp, L.; Chang, J.; Chevallier, F.; Chini, L. P.; Ciais, P.; Fader, M.; Feely, R. A.; Gkritzalis, T.; Harris, I.; Hauck, J.; Ilyina, T.; Jain, A. K.; Kato, E.; Kitidis, V.; Klein Goldewijk, K.; Koven, C.; Landschützer, P.; Lauvset, S. K.; Lefèvre, N.; Lenton, A.; Lima, I. D.; Metzl, N.; Millero, F.; Munro, D. R.; Murata, A.; Nabel, J. E. M. S.; Nakaoka, S.; Nojiri, Y.; O'Brien, K.; Olsen, A.; Ono, T.; Pérez, F. F.; Pfeil, B.; Pierrot, D.; Poulter, B.; Rehder, G.; Rödenbeck, C.; Saito, S.; Schuster, U.; Schwinger, J.; Séférian, R.; Steinhoff, T.; Stocker, B. D.; Sutton, A. J.; Takahashi, T.; Tilbrook, B.; van der Laan-Luijkx, I. T.; van der Werf, G. R.; van Heuven, S.; Vandemark, D.; Viovy, N.; Wiltshire, A.; Zaehle, S.; Zeng, N.

    2015-12-01

    carbon budget. For the last decade available (2005-2014), EFF was 9.0 ± 0.5 GtC yr-1, ELUC was 0.9 ± 0.5 GtC yr-1, GATM was 4.4 ± 0.1 GtC yr-1, SOCEAN was 2.6 ± 0.5 GtC yr-1, and SLAND was 3.0 ± 0.8 GtC yr-1. For the year 2014 alone, EFF grew to 9.8 ± 0.5 GtC yr-1, 0.6 % above 2013, continuing the growth trend in these emissions, albeit at a slower rate compared to the average growth of 2.2 % yr-1 that took place during 2005-2014. Also, for 2014, ELUC was 1.1 ± 0.5 GtC yr-1, GATM was 3.9 ± 0.2 GtC yr-1, SOCEAN was 2.9 ± 0.5 GtC yr-1, and SLAND was 4.1 ± 0.9 GtC yr-1. GATM was lower in 2014 compared to the past decade (2005-2014), reflecting a larger SLAND for that year. The global atmospheric CO2 concentration reached 397.15 ± 0.10 ppm averaged over 2014. For 2015, preliminary data indicate that the growth in EFF will be near or slightly below zero, with a projection of -0.6 [range of -1.6 to +0.5] %, based on national emissions projections for China and the USA, and projections of gross domestic product corrected for recent changes in the carbon intensity of the global economy for the rest of the world. From this projection of EFF and assumed constant ELUC for 2015, cumulative emissions of CO2 will reach about 555 ± 55 GtC (2035 ± 205 GtCO2) for 1870-2015, about 75 % from EFF and 25 % from ELUC. This living data update documents changes in the methods and data sets used in this new carbon budget compared with previous publications of this data set (Le Quéré et al., 2015, 2014, 2013). All observations presented here can be downloaded from the Carbon Dioxide Information Analysis Center (doi:10.3334/CDIAC/GCP_2015).

  7. Global Carbon Budget 2015

    SciTech Connect

    Le Quéré, C.; Moriarty, R.; Andrew, R. M.; Canadell, J. G.; Sitch, S.; Korsbakken, J. I.; Friedlingstein, P.; Peters, G. P.; Andres, R. J.; Boden, T. A.; Houghton, R. A.; House, J. I.; Keeling, R. F.; Tans, P.; Arneth, A.; Bakker, D. C. E.; Barbero, L.; Bopp, L.; Chang, J.; Chevallier, F.; Chini, L. P.; Ciais, P.; Fader, M.; Gkritzalis, T.; Harris, I.; Hauck, J.; Ilyina, T.; Jain, A. K.; Kato, E.; Kitidis, V.; Klein Goldewijk, K.; Landschützer, P.; Lauvset, S. K.; Lefèvre, N.; Lenton, A.; Lima, I. D.; Metzl, N.; Millero, F.; Munro, D. R.; Murata, A.; Nabel, J. E. M. S.; Nakaoka, S.; Nojiri, Y.; O'Brien, K.; Olsen, A.; Ono, T.; Pérez, F. F.; Pfeil, B.; Pierrot, D.; Poulter, B.; Rehder, G.; Rödenbeck, C.; Saito, S.; Schuster, U.; Schwinger, J.; Séférian, R.; Steinhoff, T.; Stocker, B. D.; Sutton, A. J.; Takahashi, T.; Tilbrook, B.; van der Laan-Luijkx, I. T.; van der Werf, G. R.; van Heuven, S.; Vandemark, D.; Viovy, N.; Wiltshire, A.; Zaehle, S.; Zeng, N.

    2015-12-07

    atmospheric inverse methods for three broad latitude bands. All uncertainties are reported as ±1σ, reflecting the current capacity to characterise the annual estimates of each component of the global carbon budget. For the last decade available (2005–2014), EFF was 9.0 ± 0.5 GtC yr-1, ELUC was 0.9 ± 0.5 GtC yr-1, GATM was 4.4 ± 0.1 GtC yr-1, SOCEAN was 2.6 ± 0.5 GtC yr-1, and SLAND was 3.0 ± 0.8 GtC yr-1. For the year 2014 alone, EFF grew to 9.8 ± 0.5 GtC yr-1, 0.6 % above 2013, continuing the growth trend in these emissions, albeit at a slower rate compared to the average growth of 2.2 % yr-1 that took place during 2005–2014. Also, for 2014, ELUC was 1.1 ± 0.5 GtC yr-1, GATM was 3.9 ± 0.2 GtC yr-1, SOCEAN was 2.9 ± 0.5 GtC yr-1, and SLAND was 4.1 ± 0.9 GtC yr-1. GATM was lower in 2014 compared to the past decade (2005–2014), reflecting a larger SLAND for that year. The global atmospheric CO2 concentration reached 397.15 ± 0.10 ppm averaged over 2014. For 2015, preliminary data indicate that the growth in EFF will be near or slightly below zero, with a projection of -0.6 [range of -1.6 to +0.5] %, based on national emissions projections for China and the USA, and projections of gross domestic product corrected for recent changes in the carbon intensity of the global economy for the rest of the world. From this projection of EFF and assumed constant ELUC for 2015, cumulative emissions of CO2 will reach about 555 ± 55 GtC (2035 ± 205 GtCO2) for 1870–2015, about 75 % from EFF and 25 % from ELUC. Finally

  8. Application of carbon nanomaterial as a microwave absorber.

    PubMed

    Sharon, Maheshwar; Pradhan, Debabrata; Zacharia, Renju; Puri, Vijaya

    2005-12-01

    Microwave absorption (8 GHz to 12 GHz) studies have been made with carbon nanomaterials for the first time. Carbon nanomaterials are synthesized by the pyrolysis of camphor. It is observed that film of carbon prepared under certain synthetic condition, can absorb microwave of either some specific wavelengths e.g., 9.5 GHz and 11.5 GHz or full range from 8-12 GHz to the extent of 20 dB depending upon their preparation condition. Carbon nanobeads seems to absorb the microwave in the range of 8-12 GHz.

  9. Organic carbon inventories in natural and restored Ecuadorian mangrove forests.

    PubMed

    DelVecchia, Amanda G; Bruno, John F; Benninger, Larry; Alperin, Marc; Banerjee, Ovik; de Dios Morales, Juan

    2014-01-01

    Mangroves can capture and store organic carbon and their protection and therefore their restoration is a component of climate change mitigation. However, there are few empirical measurements of long-term carbon storage in mangroves or of how storage varies across environmental gradients. The context dependency of this process combined with geographically limited field sampling has made it difficult to generalize regional and global rates of mangrove carbon sequestration. This has in turn hampered the inclusion of sequestration by mangroves in carbon cycle models and in carbon offset markets. The purpose of this study was to estimate the relative carbon capture and storage potential in natural and restored mangrove forests. We measured depth profiles of soil organic carbon content in 72 cores collected from six sites (three natural, two restored, and one afforested) surrounding Muisne, Ecuador. Samples up to 1 m deep were analyzed for organic matter content using loss-on-ignition and values were converted to organic carbon content using an accepted ratio of 1.72 (g/g). Results suggest that average soil carbon storage is 0.055 ± 0.002 g cm(-3) (11.3 ± 0.8% carbon content by dry mass, mean ± 1 SE) up to 1 m deep in natural sites, and 0.058 ± 0.002 g cm(-3) (8.0 ± 0.3%) in restored sites. These estimates are concordant with published global averages. Evidence of equivalent carbon stocks in restored and afforested mangrove patches emphasizes the carbon sink potential for reestablished mangrove systems. We found no relationship between sediment carbon storage and aboveground biomass, forest structure, or within-patch location. Our results demonstrate the long-term carbon storage potential of natural mangroves, high effectiveness of mangrove restoration and afforestation, a lack of predictability in carbon storage strictly based on aboveground parameters, and the need to establish standardized protocol for quantifying mangrove sediment carbon stocks. PMID:24883249

  10. Organic carbon inventories in natural and restored Ecuadorian mangrove forests

    PubMed Central

    Bruno, John F.; Benninger, Larry; Alperin, Marc; de Dios Morales, Juan

    2014-01-01

    Mangroves can capture and store organic carbon and their protection and therefore their restoration is a component of climate change mitigation. However, there are few empirical measurements of long-term carbon storage in mangroves or of how storage varies across environmental gradients. The context dependency of this process combined with geographically limited field sampling has made it difficult to generalize regional and global rates of mangrove carbon sequestration. This has in turn hampered the inclusion of sequestration by mangroves in carbon cycle models and in carbon offset markets. The purpose of this study was to estimate the relative carbon capture and storage potential in natural and restored mangrove forests. We measured depth profiles of soil organic carbon content in 72 cores collected from six sites (three natural, two restored, and one afforested) surrounding Muisne, Ecuador. Samples up to 1 m deep were analyzed for organic matter content using loss-on-ignition and values were converted to organic carbon content using an accepted ratio of 1.72 (g/g). Results suggest that average soil carbon storage is 0.055 ± 0.002 g cm−3 (11.3 ± 0.8% carbon content by dry mass, mean ± 1 SE) up to 1 m deep in natural sites, and 0.058 ± 0.002 g cm−3 (8.0 ± 0.3%) in restored sites. These estimates are concordant with published global averages. Evidence of equivalent carbon stocks in restored and afforested mangrove patches emphasizes the carbon sink potential for reestablished mangrove systems. We found no relationship between sediment carbon storage and aboveground biomass, forest structure, or within-patch location. Our results demonstrate the long-term carbon storage potential of natural mangroves, high effectiveness of mangrove restoration and afforestation, a lack of predictability in carbon storage strictly based on aboveground parameters, and the need to establish standardized protocol for quantifying mangrove sediment carbon stocks. PMID:24883249

  11. Carbon fuel cells with carbon corrosion suppression

    DOEpatents

    Cooper, John F.

    2012-04-10

    An electrochemical cell apparatus that can operate as either a fuel cell or a battery includes a cathode compartment, an anode compartment operatively connected to the cathode compartment, and a carbon fuel cell section connected to the anode compartment and the cathode compartment. An effusion plate is operatively positioned adjacent the anode compartment or the cathode compartment. The effusion plate allows passage of carbon dioxide. Carbon dioxide exhaust channels are operatively positioned in the electrochemical cell to direct the carbon dioxide from the electrochemical cell.

  12. Accelerating Mineral Carbonation Using Carbonic Anhydrase.

    PubMed

    Power, Ian M; Harrison, Anna L; Dipple, Gregory M

    2016-03-01

    Carbonic anhydrase (CA) enzymes have gained considerable attention for their potential use in carbon dioxide (CO2) capture technologies because they are able to catalyze rapidly the interconversion of aqueous CO2 and bicarbonate. However, there are challenges for widespread implementation including the need to develop mineralization process routes for permanent carbon storage. Mineral carbonation of highly reactive feedstocks may be limited by the supply rate of CO2. This rate limitation can be directly addressed by incorporating enzyme-catalyzed CO2 hydration. This study examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams on the carbonation rate of brucite [Mg(OH)2], a highly reactive mineral. Alkaline brucite slurries were amended with BCA and supplied with 10% CO2 gas while aqueous chemistry and solids were monitored throughout the experiments (hours to days). In comparison to controls, brucite carbonation using BCA was accelerated by up to 240%. Nesquehonite [MgCO3·3H2O] precipitation limited the accumulation of hydrated CO2 species, apparently preventing BCA from catalyzing the dehydration reaction. Geochemical models reproduce observed reaction progress in all experiments, revealing a linear correlation between CO2 uptake and carbonation rate. Data demonstrates that carbonation in BCA-amended reactors remained limited by CO2 supply, implying further acceleration is possible.

  13. Accelerating Mineral Carbonation Using Carbonic Anhydrase.

    PubMed

    Power, Ian M; Harrison, Anna L; Dipple, Gregory M

    2016-03-01

    Carbonic anhydrase (CA) enzymes have gained considerable attention for their potential use in carbon dioxide (CO2) capture technologies because they are able to catalyze rapidly the interconversion of aqueous CO2 and bicarbonate. However, there are challenges for widespread implementation including the need to develop mineralization process routes for permanent carbon storage. Mineral carbonation of highly reactive feedstocks may be limited by the supply rate of CO2. This rate limitation can be directly addressed by incorporating enzyme-catalyzed CO2 hydration. This study examined the effects of bovine carbonic anhydrase (BCA) and CO2-rich gas streams on the carbonation rate of brucite [Mg(OH)2], a highly reactive mineral. Alkaline brucite slurries were amended with BCA and supplied with 10% CO2 gas while aqueous chemistry and solids were monitored throughout the experiments (hours to days). In comparison to controls, brucite carbonation using BCA was accelerated by up to 240%. Nesquehonite [MgCO3·3H2O] precipitation limited the accumulation of hydrated CO2 species, apparently preventing BCA from catalyzing the dehydration reaction. Geochemical models reproduce observed reaction progress in all experiments, revealing a linear correlation between CO2 uptake and carbonation rate. Data demonstrates that carbonation in BCA-amended reactors remained limited by CO2 supply, implying further acceleration is possible. PMID:26829491

  14. 40 CFR 721.10420 - Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569). 721.10420 Section 721.10420 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10420 Fluoropolymers (generic) (P-11-567,...

  15. 40 CFR 721.10420 - Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569). 721.10420 Section 721.10420 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10420 Fluoropolymers (generic) (P-11-567,...

  16. 40 CFR 721.10420 - Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Fluoropolymers (generic) (P-11-567, P-11-568, and P-11-569). 721.10420 Section 721.10420 Protection of Environment ENVIRONMENTAL PROTECTION... New Uses for Specific Chemical Substances § 721.10420 Fluoropolymers (generic) (P-11-567,...

  17. Neoplastic Transformation Induced by Carbon Ions

    SciTech Connect

    Bettega, Daniela Calzolari, Paola; Hessel, Petra; Stucchi, Claudio G.; Weyrather, Wilma K.

    2009-03-01

    Purpose: The objective of this experiment was to compare the oncogenic potential of carbon ion beams and conventional photon beams for use in radiotherapy. Methods and Materials: The HeLa X human skin fibroblast cell line CGL1 was irradiated with carbon ions of three different energies (270, 100, and 11.4 MeV/u). Inactivation and transformation data were compared with those for 15 MeV photons. Results: Inactivation and transformation frequencies for the 270 MeV/u carbon ions were similar to those for 15-MeV photons. The maximal relative biologic effectiveness (RBE{sub {alpha}}) values for 100MeV/u and 11.4 MeV/u carbon ions, respectively, were as follows: inactivation, 1.6 {+-} 0.2 and 6.7 {+-} 0.7; and transformation per surviving cell, 2.5 {+-} 0.6 and 12 {+-} 3. The curve for dose-transformation per cell at risk exhibited a maximum that was shifted toward lower doses at lower energies. Conclusions: Transformation induction per cell at risk for carbon ions in the entrance channel was comparable to that for photons, whereas for the lower energies, 100 MeV/u and 11 MeV/u, which are representative of the energies delivered to the tumor margins and volume, respectively, the probability of transformation in a single cell was greater than it was for photons. In addition, at isoeffective doses with respect to cell killing, the 11.4-MeV/u beam was more oncogenic than were photons.

  18. [11C]PR04.MZ, a promising DAT ligand for low concentration imaging: synthesis, efficient 11C-0-methylation and initial small animal PET studies

    SciTech Connect

    Riss, P.J.; Hooker, J.; Alexoff, D.; Kim, Sung-Won; Fowler, J.S.; Roesch, F.

    2009-05-01

    PR04.MZ was designed as a highly selective dopamine transporter inhibitor, derived from natural cocaine. Its binding profile indicates that [{sup 11}C]PR04.MZ may be suited as a PET radioligand for the non-invasive exploration of striatal and extrastriatal DAT populations. As a key feature, its structural design facilitates both, labelling with fluorine-18 at its terminally fluorinated butynyl moiety and carbon-11 at its methyl ester function. The present report concerns the efficient [{sup 11}C]MeI mediated synthesis of [{sup 11}C]PR04.MZ from an O-desmethyl precursor trifluoroacetic acid salt with Rb{sub 2}CO{sub 3} in DMF in up to 95 {+-} 5% labelling yield. A preliminary {mu}PET-experiment demonstrates the reversible, highly specific binding of [{sup 11}C]PR04.MZ in the brain of a male Sprague-Dawley rat.

  19. Understanding Geochemical Impacts of Carbon Dioxide Leakage from Carbon Capture and Sequestration

    EPA Science Inventory

    US EPA held a technical Geochemical Impact Workshop in Washington, DC on July 10 and 11, 2007 to discuss geological considerations and Area of Review (AoR) issues related to geologic sequestration (GS) of Carbon Dioxide (CO2). Seventy=one (71) representatives of the electric uti...

  20. Metallic carbon materials

    DOEpatents

    Cohen, Marvin Lou; Crespi, Vincent Henry; Louie, Steven Gwon Sheng; Zettl, Alexander Karlwalter

    1999-01-01

    Novel metallic forms of planar carbon are described, as well as methods of designing and making them. Nonhexagonal arrangements of carbon are introduced into a graphite carbon network essentially without destroying the planar structure. Specifically a form of carbon comprising primarily pentagons and heptagons, and having a large density of states at the Fermi level is described. Other arrangements of pentagons and heptagons that include some hexagons, and structures incorporating squares and octagons are additionally disclosed. Reducing the bond angle symmetry associated with a hexagonal arrangement of carbons increases the likelihood that the carbon material will have a metallic electron structure.

  1. Bion 11 mission: primate experiments

    NASA Technical Reports Server (NTRS)

    Ilyin, E. A.; Korolkov, V. I.; Skidmore, M. G.; Viso, M.; Kozlovskaya, I. B.; Grindeland, R. E.; Lapin, B. A.; Gordeev, Y. V.; Krotov, V. P.; Fanton, J. W.; Bielitzki, J. T.; Golov, V. K.; Magedov, V. S.; Hines, J. W.

    2000-01-01

    A summary is provided of the major operations required to conduct the wide range of primate experiments on the Bion 11 mission, which flew for 14 days beginning December 24, 1996. Information is given on preflight preparations, including flight candidate selection and training; attachment and implantation of bioinstrumentation; flight and ground experiment designs; onboard life support and test systems; ground and flight health monitoring; flight monkey selection and transport to the launch site; inflight procedures and data collection; postflight examinations and experiments; and assessment of results.

  2. Apollo 11 soil mechanics investigation.

    PubMed

    Costes, N C; Carrier, W D; Mitchell, J K; Scott, R F

    1970-01-30

    The fine-grained surface material at the Apollo 11 landing site is a brownish, medium-gray, slightly cohesive granular soil, with bulky grains in the silt-to-fine-sand range, having a specific gravity of 3.1 and exhibiting adhesive characteristics. Within the upper few centimeters, the lunar soil has an average density of about 1.6 grams per cubic centimeter and is similar in appearance and behavior to the soils studied at the Surveyor equatorial landing sites. Althouglh considerably different in composition and in range of particle shapes, it is similar in its mechanical behavior to terrestrial soils of the same grain size distribution.

  3. Bion 11 mission: primate experiments.

    PubMed

    Ilyin, E A; Korolkov, V I; Skidmore, M G; Viso, M; Kozlovskaya, I B; Grindeland, R E; Lapin, B A; Gordeev, Y V; Krotov, V P; Fanton, J W; Bielitzki, J T; Golov, V K; Magedov, V S; Hines, J W

    2000-01-01

    A summary is provided of the major operations required to conduct the wide range of primate experiments on the Bion 11 mission, which flew for 14 days beginning December 24, 1996. Information is given on preflight preparations, including flight candidate selection and training; attachment and implantation of bioinstrumentation; flight and ground experiment designs; onboard life support and test systems; ground and flight health monitoring; flight monkey selection and transport to the launch site; inflight procedures and data collection; postflight examinations and experiments; and assessment of results.

  4. Carbon sequestration rate and aboveground biomass carbon potential of three young species in lower Gangetic plain.

    PubMed

    Jana, Bipal K; Biswas, Soumyajit; Majumder, Mrinmoy; Roy, Pankaj K; Mazumdar, Asis

    2011-07-01

    Carbon is sequestered by the plant photosynthesis and stored as biomass in different parts of the tree. Carbon sequestration rate has been measured for young species (6 years age) of Shorea robusta at Chadra forest in Paschim Medinipur district, Albizzia lebbek in Indian Botanic Garden in Howrah district and Artocarpus integrifolia at Banobitan within Kolkata in the lower Gangetic plain of West Bengal in India by Automated Vaisala Made Instrument GMP343 and aboveground biomass carbon has been analyzed by CHN analyzer. The specific objective of this paper is to measure carbon sequestration rate and aboveground biomass carbon potential of three young species of Shorea robusta, Albizzia lebbek and Artocarpus integrifolia. The carbon sequestration rate (mean) from the ambient air during winter season as obtained by Shorea robusta, Albizzia lebbek and Artocarpus integrifolia were 11.13 g/h, 14.86 g/h and 4.22g/h, respectively. The annual carbon sequestration rate from ambient air were estimated at 8.97 t C ha(-1) by Shorea robusta, 11.97 t C ha(-1) by Albizzia lebbek and 3.33 t C ha(-1) by Artocarpus integrifolia. The percentage of carbon content (except root) in the aboveground biomass of Shorea robusta, Albizzia lebbek and Artocarpus integrifolia were 47.45, 47.12 and 43.33, respectively. The total aboveground biomass carbon stock per hectare as estimated for Shorea robusta, Albizzia lebbek and Artocarpus integrifolia were 5.22 t C ha(-1) , 6.26 t C ha(-1) and 7.28 t C ha(-1), respectively in these forest stands.

  5. 37 CFR 11.11 - Administrative suspension, inactivation, resignation, and readmission.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Administrative suspension, inactivation, resignation, and readmission. 11.11 Section 11.11 Patents, Trademarks, and Copyrights UNITED... Other Non-Patent Law § 11.11 Administrative suspension, inactivation, resignation, and readmission....

  6. 37 CFR 11.11 - Administrative suspension, inactivation, resignation, and readmission.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2013-07-01 2013-07-01 false Administrative suspension, inactivation, resignation, and readmission. 11.11 Section 11.11 Patents, Trademarks, and Copyrights UNITED... Other Non-Patent Law § 11.11 Administrative suspension, inactivation, resignation, and readmission....

  7. 37 CFR 11.11 - Administrative suspension, inactivation, resignation, and readmission.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2012-07-01 2012-07-01 false Administrative suspension, inactivation, resignation, and readmission. 11.11 Section 11.11 Patents, Trademarks, and Copyrights UNITED... Other Non-Patent Law § 11.11 Administrative suspension, inactivation, resignation, and readmission....

  8. 37 CFR 11.11 - Administrative suspension, inactivation, resignation, and readmission.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2011-07-01 2011-07-01 false Administrative suspension, inactivation, resignation, and readmission. 11.11 Section 11.11 Patents, Trademarks, and Copyrights UNITED... Other Non-Patent Law § 11.11 Administrative suspension, inactivation, resignation, and readmission....

  9. 37 CFR 11.11 - Administrative suspension, inactivation, resignation, and readmission.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2014-07-01 2014-07-01 false Administrative suspension, inactivation, resignation, and readmission. 11.11 Section 11.11 Patents, Trademarks, and Copyrights UNITED... Other Non-Patent Law § 11.11 Administrative suspension, inactivation, resignation, and readmission....

  10. High rates of organic carbon burial in fjord sediments globally

    NASA Astrophysics Data System (ADS)

    Smith, Richard W.; Bianchi, Thomas S.; Allison, Mead; Savage, Candida; Galy, Valier

    2015-06-01

    The deposition and long-term burial of organic carbon in marine sediments has played a key role in controlling atmospheric O2 and CO2 concentrations over the past 500 million years. Marine carbon burial represents the dominant natural mechanism of long-term organic carbon sequestration. Fjords--deep, glacially carved estuaries at high latitudes--have been hypothesized to be hotspots of organic carbon burial, because they receive high rates of organic material fluxes from the watershed. Here we compile organic carbon concentrations from 573 fjord surface sediment samples and 124 sediment cores from nearly all fjord systems globally. We use sediment organic carbon content and sediment delivery rates to calculate rates of organic carbon burial in fjord systems across the globe. We estimate that about 18 Mt of organic carbon are buried in fjord sediments each year, equivalent to 11% of annual marine carbon burial globally. Per unit area, fjord organic carbon burial rates are one hundred times as large as the global ocean average, and fjord sediments contain twice as much organic carbon as biogenous sediments underlying the upwelling regions of the ocean. We conclude that fjords may play an important role in climate regulation on glacial-interglacial timescales.

  11. 7 CFR 1739.11 - Eligible project.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 7 Agriculture 11 2013-01-01 2013-01-01 false Eligible project. 1739.11 Section 1739.11 Agriculture... BROADBAND GRANT PROGRAM Community Connect Grant Program § 1739.11 Eligible project. To be eligible for a grant, the Project must: (a) Serve a Rural Area where Broadband Transmission Service does not...

  12. 7 CFR 1739.11 - Eligible project.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 11 2011-01-01 2011-01-01 false Eligible project. 1739.11 Section 1739.11 Agriculture... BROADBAND GRANT PROGRAM Community Connect Grant Program § 1739.11 Eligible project. To be eligible for a grant, the Project must: (a) Serve a Rural Area where Broadband Transmission Service does not...

  13. 7 CFR 1739.11 - Eligible project.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 7 Agriculture 11 2012-01-01 2012-01-01 false Eligible project. 1739.11 Section 1739.11 Agriculture... BROADBAND GRANT PROGRAM Community Connect Grant Program § 1739.11 Eligible project. To be eligible for a grant, the Project must: (a) Serve a Rural Area where Broadband Transmission Service does not...

  14. 50 CFR 296.11 - Final determination.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 50 Wildlife and Fisheries 11 2013-10-01 2013-10-01 false Final determination. 296.11 Section 296.11 Wildlife and Fisheries NATIONAL MARINE FISHERIES SERVICE, NATIONAL OCEANIC AND ATMOSPHERIC ADMINISTRATION, DEPARTMENT OF COMMERCE CONTINENTAL SHELF FISHERMEN'S CONTINGENCY FUND § 296.11...

  15. 11 CFR 300.2 - Definitions.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... connection with a Federal election as that term is used in 11 CFR 300.11, 300.37, 300.50, and 300.51 includes... a public communication (see 11 CFR 100.26). (c) Directly or indirectly establish, finance, maintain... its allocated share of proceeds jointly raised pursuant to 11 CFR 102.17, and otherwise...

  16. 11 CFR 300.2 - Definitions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... connection with a Federal election as that term is used in 11 CFR 300.11, 300.37, 300.50, and 300.51 includes... a public communication (see 11 CFR 100.26). (c) Directly or indirectly establish, finance, maintain... its allocated share of proceeds jointly raised pursuant to 11 CFR 102.17, and otherwise...

  17. 11 CFR 300.2 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... connection with a Federal election as that term is used in 11 CFR 300.11, 300.37, 300.50, and 300.51 includes... a public communication (see 11 CFR 100.26). (c) Directly or indirectly establish, finance, maintain... its allocated share of proceeds jointly raised pursuant to 11 CFR 102.17, and otherwise...

  18. 11 CFR 300.2 - Definitions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... connection with a Federal election as that term is used in 11 CFR 300.11, 300.37, 300.50, and 300.51 includes... a public communication (see 11 CFR 100.26). (c) Directly or indirectly establish, finance, maintain... its allocated share of proceeds jointly raised pursuant to 11 CFR 102.17, and otherwise...

  19. 11 CFR 300.2 - Definitions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... connection with a Federal election as that term is used in 11 CFR 300.11, 300.37, 300.50, and 300.51 includes... a public communication (see 11 CFR 100.26). (c) Directly or indirectly establish, finance, maintain... its allocated share of proceeds jointly raised pursuant to 11 CFR 102.17, and otherwise...

  20. 47 CFR 11.33 - EAS Decoder.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 47 Telecommunication 1 2013-10-01 2013-10-01 false EAS Decoder. 11.33 Section 11.33 Telecommunication FEDERAL COMMUNICATIONS COMMISSION GENERAL EMERGENCY ALERT SYSTEM (EAS) Equipment Requirements § 11.33 EAS Decoder. (a) An EAS Decoder must at a minimum be capable of providing the EAS monitoring functions described in § 11.52, decoding...

  1. 47 CFR 11.33 - EAS Decoder.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 47 Telecommunication 1 2014-10-01 2014-10-01 false EAS Decoder. 11.33 Section 11.33 Telecommunication FEDERAL COMMUNICATIONS COMMISSION GENERAL EMERGENCY ALERT SYSTEM (EAS) Equipment Requirements § 11.33 EAS Decoder. (a) An EAS Decoder must at a minimum be capable of providing the EAS monitoring functions described in § 11.52, decoding...

  2. 47 CFR 11.33 - EAS Decoder.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 47 Telecommunication 1 2011-10-01 2011-10-01 false EAS Decoder. 11.33 Section 11.33 Telecommunication FEDERAL COMMUNICATIONS COMMISSION GENERAL EMERGENCY ALERT SYSTEM (EAS) Equipment Requirements § 11.33 EAS Decoder. (a) An EAS Decoder must at a minimum be capable of decoding the EAS protocol described in § 11.31, provide the EAS...

  3. 7 CFR 1739.11 - Eligible project.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 11 2010-01-01 2010-01-01 false Eligible project. 1739.11 Section 1739.11 Agriculture... BROADBAND GRANT PROGRAM Community Connect Grant Program § 1739.11 Eligible project. To be eligible for a grant, the Project must: (a) Serve a Rural Area where Broadband Transmission Service does not...

  4. 11 CFR 116.10 - Disputed debts.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... political committee may have against the creditor. (See also 11 CFR 9035.1(a)(2) regarding the effect of disputed debts on a candidate's expenditure limitations under 11 CFR part 9035.) (b) Disputed debts owed by... accordance with 11 CFR 104.3(d) and 104.11 if the creditor has provided something of value to the...

  5. 11 CFR 116.10 - Disputed debts.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... accordance with 11 CFR 104.3(d) and 104.11 if the creditor has provided something of value to the political... political committee may have against the creditor. (See also 11 CFR 9035.1(a)(2) regarding the effect of disputed debts on a candidate's expenditure limitations under 11 CFR part 9035.) (b) Disputed debts owed...

  6. 11 CFR 9036.5 - Resubmissions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... the submission review pursuant to 11 CFR 9036.4(b), or of an inquiry pursuant to 11 CFR 9039.3 that... presentation of resubmissions. If the candidate chooses to resubmit any contributions under 11 CFR 9036.5(a... specified in 11 CFR 9036.2(b)(1), except that: (1) The candidate need not provide photocopies of...

  7. Method of making carbon-carbon composites

    DOEpatents

    Engle, Glen B.

    1991-01-01

    A process for making a carbon-carbon composite having a combination of high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizable woven cloth are covered with petroleum or coal tar pitch and pressed at a temperature a few degrees above the softening point of the pitch to form a green laminated composite. The green composite is restrained in a suitable fixture and heated slowly to carbonize the pitch binder. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnation step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500.degree. to 3000.degree. C. to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000.degree. to 1300.degree. C. at a reduced pressure for approximately one hundred and fifty (150) hours.

  8. A Symbiosis: Carbon Monitoring and Carbon Management

    NASA Astrophysics Data System (ADS)

    Macauley, M.

    2015-12-01

    "We measure what we value and value what we measure." This old dictum characterizes the usefulness of carbon monitoring in serving society, both in advancing research on carbon cycles and in applying new scientific knowledge to help carbon management. Many attempts to design policy for carbon management have been limited, ineffective, or otherwise unsuccessful in part due to inadequate capacity to observe carbon sources and sinks with sufficient measurement certainty and at appropriate spatial scale. Too often, policy designers fail to understand the complexities of carbon science and carbon researchers fail to align at least a portion of their science goals with policy requirements. The carbon monitoring systems research and applications activities under the auspices of the US National Aeronautics and Space Administration have significantly advanced both science and applications. To further this necessary symbiosis, this paper will synthesize current and prospective spatial and temporal requirements for emerging policy needs, discuss likely requirements for measurement certainty, and draw lessons from experiences in policies designed to monitor and manage other natural resources for which scientific research necessarily influenced policy design and effectiveness.

  9. Method of making carbon-carbon composites

    SciTech Connect

    Engle, G.B.

    1991-10-29

    A process is described for making a carbon-carbon composite having a combination of high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizable woven cloth are covered with petroleum or coal tar pitch and pressed at a temperature a few degrees above the softening point of the pitch to form a green laminated composite. The green composite is restrained in a suitable fixture and heated slowly to carbonize the pitch binder. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnation step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500 to 3000 C to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000 to 1300 C at a reduced pressure for approximately one hundred and fifty (150) hours.

  10. Quarantined Apollo 11 Crew Debriefing

    NASA Technical Reports Server (NTRS)

    1969-01-01

    The Apollo 11 mission, the first manned lunar mission, launched from the Kennedy Space Center, Florida via the Marshall Space Flight Center (MSFC) developed Saturn V launch vehicle on July 16, 1969 and safely returned to Earth on July 24, 1969. Aboard the space craft were astronauts Neil A. Armstrong, commander; Michael Collins, Command Module (CM) pilot; and Edwin E. Aldrin Jr., Lunar Module (LM) pilot. The CM, piloted by Michael Collins remained in a parking orbit around the Moon while the LM, named 'Eagle'', carrying astronauts Neil Armstrong and Edwin Aldrin, landed on the Moon. During 2½ hours of surface exploration, the crew collected 47 pounds of lunar surface material for analysis back on Earth. The recovery operation took place in the Pacific Ocean where Navy para-rescue men recovered the capsule housing the 3-man Apollo 11 crew. The crew was airlifted to safety aboard the U.S.S. Hornet, where they were quartered in a Mobile Quarantine Facility (MQF) which served as their home until they reached the NASA Manned Spacecraft Center (MSC) Lunar Receiving Laboratory in Houston, Texas. The three are seen here at the MSC, still inside the MQF, undergoing their first debriefing on Sunday, August 3, 1969. Behind the glass are (L-R): Edwin Aldrin, Michael Collins, and Neil Armstrong.

  11. Carbon Nanotubes for Polymer Photovoltaics

    NASA Astrophysics Data System (ADS)

    Anctil, Annick; Dileo, Roberta; Schauerman, Chris; Landi, Brian; Raffaelle, Ryne

    2007-03-01

    Carbon nanotubes are being investigated for optical absorption, exciton dissociation, and carrier transport in polymer photovoltaic devices. In the present work, single wall carbon nanotubes (SWNTs) were synthesized by an Alexandrite pulsed laser vaporization reactor at standard conditions and purified based upon our previously reported TOP procedure. The SWNTs were dispersed in polymer composites for pure MEH-PPV, pure P3HT, and [C60]-PCBM-P3HT (1:1 by weight) as a function of nanotube weight loading (0.1 -- 5% w/w). The AM0 current-voltage measurements for structures sandwiched between PEDOT/PSS coated ITO substrates and an evaporated aluminum contact demonstrate the dramatic effect of SWNT content on the short circuit current density, with conversions efficiencies consistently greater than 1%. The temperature coefficient for nanotube-containing polymer photovoltaics has been compared to conventional PCBM-P3HT devices, and the general relationship of increasing efficiency with increasing temperature is observed. However, the necessity to control nanotube percolation to prevent device shunting has led to recent developments which focus on controlling nanotube length through oxidative cutting, the deposition of intrinsic polymer layers, and the use of aligned carbon nanotube arrays for preferential charge transport.

  12. Development of a NiO target for the production of 11C at ISAC/TRIUMF

    NASA Astrophysics Data System (ADS)

    Bricault, Pierre G.; Ames, Friedhelm; Dombsky, Marik; Kunz, Peter; Lassen, Jens; Mjøs, Anders; Wong, John

    2016-01-01

    High intensity 11C beams are necessary for the investigation of the formation of 12C via the nuclear reaction 11C(p, γ)12N → 12C + e+ + ν. The production of intense carbon beams on-line is quite challenging due to the thermodynamic properties and chemical reactivity of carbon at high temperatures. A previous attempt, using a medical isotope cyclotron production method in batch mode, was not conclusive. The intensity obtained was at least one order of magnitude too low for a direct proton capture experiment using the DRAGON facility at ISAC/TRIUMF. Producing a 11C beams using the ISOL method requires a target capable of efficiently releasing the carbon isotopes. NiO has been selected as a target material because most of the nickel carbides are not stable at high temperature. The development of carbon beams using a composite NiO/Ni target on-line is described.

  13. T-carbon: a novel carbon allotrope.

    PubMed

    Sheng, Xian-Lei; Yan, Qing-Bo; Ye, Fei; Zheng, Qing-Rong; Su, Gang

    2011-04-15

    A structurally stable crystalline carbon allotrope is predicted by means of the first-principles calculations. This allotrope can be derived by substituting each atom in diamond with a carbon tetrahedron, and possesses the same space group Fd3m as diamond, which is thus coined as T-carbon. The calculations on geometrical, vibrational, and electronic properties reveal that T-carbon, with a considerable structural stability and a much lower density 1.50  g/cm3, is a semiconductor with a direct band gap about 3.0 eV, and has a Vickers hardness 61.1 GPa lower than diamond but comparable with cubic boron nitride. Such a form of carbon, once obtained, would have wide applications in photocatalysis, adsorption, hydrogen storage, and aerospace materials. PMID:21568576

  14. Boron isotope fractionation in magma via crustal carbonate dissolution.

    PubMed

    Deegan, Frances M; Troll, Valentin R; Whitehouse, Martin J; Jolis, Ester M; Freda, Carmela

    2016-08-04

    Carbon dioxide released by arc volcanoes is widely considered to originate from the mantle and from subducted sediments. Fluids released from upper arc carbonates, however, have recently been proposed to help modulate arc CO2 fluxes. Here we use boron as a tracer, which substitutes for carbon in limestone, to further investigate crustal carbonate degassing in volcanic arcs. We performed laboratory experiments replicating limestone assimilation into magma at crustal pressure-temperature conditions and analysed boron isotope ratios in the resulting experimental glasses. Limestone dissolution and assimilation generates CaO-enriched glass near the reaction site and a CO2-dominated vapour phase. The CaO-rich glasses have extremely low δ(11)B values down to -41.5‰, reflecting preferential partitioning of (10)B into the assimilating melt. Loss of (11)B from the reaction site occurs via the CO2 vapour phase generated during carbonate dissolution, which transports (11)B away from the reaction site as a boron-rich fluid phase. Our results demonstrate the efficacy of boron isotope fractionation during crustal carbonate assimilation and suggest that low δ(11)B melt values in arc magmas could flag shallow-level additions to the subduction cycle.

  15. Boron isotope fractionation in magma via crustal carbonate dissolution

    PubMed Central

    Deegan, Frances M.; Troll, Valentin R.; Whitehouse, Martin J.; Jolis, Ester M.; Freda, Carmela

    2016-01-01

    Carbon dioxide released by arc volcanoes is widely considered to originate from the mantle and from subducted sediments. Fluids released from upper arc carbonates, however, have recently been proposed to help modulate arc CO2 fluxes. Here we use boron as a tracer, which substitutes for carbon in limestone, to further investigate crustal carbonate degassing in volcanic arcs. We performed laboratory experiments replicating limestone assimilation into magma at crustal pressure-temperature conditions and analysed boron isotope ratios in the resulting experimental glasses. Limestone dissolution and assimilation generates CaO-enriched glass near the reaction site and a CO2-dominated vapour phase. The CaO-rich glasses have extremely low δ11B values down to −41.5‰, reflecting preferential partitioning of 10B into the assimilating melt. Loss of 11B from the reaction site occurs via the CO2 vapour phase generated during carbonate dissolution, which transports 11B away from the reaction site as a boron-rich fluid phase. Our results demonstrate the efficacy of boron isotope fractionation during crustal carbonate assimilation and suggest that low δ11B melt values in arc magmas could flag shallow-level additions to the subduction cycle. PMID:27488228

  16. Boron isotope fractionation in magma via crustal carbonate dissolution.

    PubMed

    Deegan, Frances M; Troll, Valentin R; Whitehouse, Martin J; Jolis, Ester M; Freda, Carmela

    2016-01-01

    Carbon dioxide released by arc volcanoes is widely considered to originate from the mantle and from subducted sediments. Fluids released from upper arc carbonates, however, have recently been proposed to help modulate arc CO2 fluxes. Here we use boron as a tracer, which substitutes for carbon in limestone, to further investigate crustal carbonate degassing in volcanic arcs. We performed laboratory experiments replicating limestone assimilation into magma at crustal pressure-temperature conditions and analysed boron isotope ratios in the resulting experimental glasses. Limestone dissolution and assimilation generates CaO-enriched glass near the reaction site and a CO2-dominated vapour phase. The CaO-rich glasses have extremely low δ(11)B values down to -41.5‰, reflecting preferential partitioning of (10)B into the assimilating melt. Loss of (11)B from the reaction site occurs via the CO2 vapour phase generated during carbonate dissolution, which transports (11)B away from the reaction site as a boron-rich fluid phase. Our results demonstrate the efficacy of boron isotope fractionation during crustal carbonate assimilation and suggest that low δ(11)B melt values in arc magmas could flag shallow-level additions to the subduction cycle. PMID:27488228

  17. Boron isotope fractionation in magma via crustal carbonate dissolution

    NASA Astrophysics Data System (ADS)

    Deegan, Frances M.; Troll, Valentin R.; Whitehouse, Martin J.; Jolis, Ester M.; Freda, Carmela

    2016-08-01

    Carbon dioxide released by arc volcanoes is widely considered to originate from the mantle and from subducted sediments. Fluids released from upper arc carbonates, however, have recently been proposed to help modulate arc CO2 fluxes. Here we use boron as a tracer, which substitutes for carbon in limestone, to further investigate crustal carbonate degassing in volcanic arcs. We performed laboratory experiments replicating limestone assimilation into magma at crustal pressure-temperature conditions and analysed boron isotope ratios in the resulting experimental glasses. Limestone dissolution and assimilation generates CaO-enriched glass near the reaction site and a CO2-dominated vapour phase. The CaO-rich glasses have extremely low δ11B values down to ‑41.5‰, reflecting preferential partitioning of 10B into the assimilating melt. Loss of 11B from the reaction site occurs via the CO2 vapour phase generated during carbonate dissolution, which transports 11B away from the reaction site as a boron-rich fluid phase. Our results demonstrate the efficacy of boron isotope fractionation during crustal carbonate assimilation and suggest that low δ11B melt values in arc magmas could flag shallow-level additions to the subduction cycle.

  18. 25 CFR 11.908 - Court records.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 25 Indians 1 2014-04-01 2014-04-01 false Court records. 11.908 Section 11.908 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Children's Court § 11.908 Court records. (a) A record of all hearings under §§ 11.900-11.1114 of this...

  19. Carbon Based Nanotechnology: Review

    NASA Technical Reports Server (NTRS)

    Srivastava, Deepak; Saini, Subhash (Technical Monitor)

    1999-01-01

    This presentation reviews publicly available information related to carbon based nanotechnology. Topics covered include nanomechanics, carbon based electronics, nanodevice/materials applications, nanotube motors, nano-lithography and H2O storage in nanotubes.

  20. Interstellar carbon in meteorites

    NASA Technical Reports Server (NTRS)

    Swart, P. K.; Grady, M. M.; Pillinger, C. T.; Lewis, R. S.; Anders, E.

    1983-01-01

    The Murchison and Allende chondrites contain up to 5 parts per million carbon that is enriched in carbon-13 by up to +1100 per mil (the ratio of carbon-12 to carbon-13 is approximately 42, compared to 88 to 93 for terrestrial carbon). This 'heavy' carbon is associated with neon-22 and with anomalous krypton and xenon showing the signature of the s-process (neutron capture on a slow time scale). It apparently represents interstellar grains ejected from late-type stars. A second anomalous xenon component ('CCFXe') is associated with a distinctive, light carbon (depleted in carbon-13 by 38 per mil), which, however, falls within the terrestrial range and hence may be of either local or exotic origin.

  1. Trading forest carbon - OSU

    EPA Science Inventory

    Issues associate with trading carbon sequestered in forests are discussed. Scientific uncertainties associated with carbon measurement are discussed with respect to proposed accounting procedures. Major issues include: (1) Establishing baselines. (2) Determining additivity from f...

  2. Carbon nanotube nanoelectrode arrays

    DOEpatents

    Ren, Zhifeng; Lin, Yuehe; Yantasee, Wassana; Liu, Guodong; Lu, Fang; Tu, Yi

    2008-11-18

    The present invention relates to microelectode arrays (MEAs), and more particularly to carbon nanotube nanoelectrode arrays (CNT-NEAs) for chemical and biological sensing, and methods of use. A nanoelectrode array includes a carbon nanotube material comprising an array of substantially linear carbon nanotubes each having a proximal end and a distal end, the proximal end of the carbon nanotubes are attached to a catalyst substrate material so as to form the array with a pre-determined site density, wherein the carbon nanotubes are aligned with respect to one another within the array; an electrically insulating layer on the surface of the carbon nanotube material, whereby the distal end of the carbon nanotubes extend beyond the electrically insulating layer; a second adhesive electrically insulating layer on the surface of the electrically insulating layer, whereby the distal end of the carbon nanotubes extend beyond the second adhesive electrically insulating layer; and a metal wire attached to the catalyst substrate material.

  3. Calcium carbonate overdose

    MedlinePlus

    Tums overdose; Calcium overdose ... Calcium carbonate can be dangerous in large amounts. ... Some products that contain calcium carbonate are certain: ... and mineral supplements Other products may also contain calcium ...

  4. Potassium carbonate poisoning

    MedlinePlus

    Potassium carbonate is a white powder used to make soap, glass, and other items. This article discusses poisoning from swallowing or breathing in potassium carbonate. This article is for information only. Do ...

  5. Not just carbon widgets

    NASA Astrophysics Data System (ADS)

    2016-08-01

    Forests are important for the global carbon cycle, and for mitigating greenhouse gas emissions. However, the role forests play in carbon sequestration should not eclipse everything else we value them for.

  6. Carbon Monoxide Information Center

    MedlinePlus

    ... Monoxide Carbon Monoxide Information Center En Español The Invisible Killer Carbon monoxide, also known as CO, is called the "Invisible Killer" because it's a colorless, odorless, poisonous gas. ...

  7. A reduced organic carbon component in martian basalts.

    PubMed

    Steele, A; McCubbin, F M; Fries, M; Kater, L; Boctor, N Z; Fogel, M L; Conrad, P G; Glamoclija, M; Spencer, M; Morrow, A L; Hammond, M R; Zare, R N; Vicenzi, E P; Siljeström, S; Bowden, R; Herd, C D K; Mysen, B O; Shirey, S B; Amundsen, H E F; Treiman, A H; Bullock, E S; Jull, A J T

    2012-07-13

    The source and nature of carbon on Mars have been a subject of intense speculation. We report the results of confocal Raman imaging spectroscopy on 11 martian meteorites, spanning about 4.2 billion years of martian history. Ten of the meteorites contain abiotic macromolecular carbon (MMC) phases detected in association with small oxide grains included within high-temperature minerals. Polycyclic aromatic hydrocarbons were detected along with MMC phases in Dar al Gani 476. The association of organic carbon within magmatic minerals indicates that martian magmas favored precipitation of reduced carbon species during crystallization. The ubiquitous distribution of abiotic organic carbon in martian igneous rocks is important for understanding the martian carbon cycle and has implications for future missions to detect possible past martian life. PMID:22628557

  8. A reduced organic carbon component in martian basalts.

    PubMed

    Steele, A; McCubbin, F M; Fries, M; Kater, L; Boctor, N Z; Fogel, M L; Conrad, P G; Glamoclija, M; Spencer, M; Morrow, A L; Hammond, M R; Zare, R N; Vicenzi, E P; Siljeström, S; Bowden, R; Herd, C D K; Mysen, B O; Shirey, S B; Amundsen, H E F; Treiman, A H; Bullock, E S; Jull, A J T

    2012-07-13

    The source and nature of carbon on Mars have been a subject of intense speculation. We report the results of confocal Raman imaging spectroscopy on 11 martian meteorites, spanning about 4.2 billion years of martian history. Ten of the meteorites contain abiotic macromolecular carbon (MMC) phases detected in association with small oxide grains included within high-temperature minerals. Polycyclic aromatic hydrocarbons were detected along with MMC phases in Dar al Gani 476. The association of organic carbon within magmatic minerals indicates that martian magmas favored precipitation of reduced carbon species during crystallization. The ubiquitous distribution of abiotic organic carbon in martian igneous rocks is important for understanding the martian carbon cycle and has implications for future missions to detect possible past martian life.

  9. Metal filled porous carbon

    DOEpatents

    Gross, Adam F.; Vajo, John J.; Cumberland, Robert W.; Liu, Ping; Salguero, Tina T.

    2011-03-22

    A porous carbon scaffold with a surface and pores, the porous carbon scaffold containing a primary metal and a secondary metal, where the primary metal is a metal that does not wet the surface of the pores of the carbon scaffold but wets the surface of the secondary metal, and the secondary metal is interspersed between the surface of the pores of the carbon scaffold and the primary metal.

  10. Final report on SNAC 11

    SciTech Connect

    Huber, Patrick

    2013-06-26

    This report details how the $5,000 DOE grant to support the workshop titled “Sterile Neutrinos at the Crossroads” (or SNAC11) was allocated and spent. The SNAC11 workshop covered three days during which there were 28 talks, multiple discussion sessions, a poster session with 9 posters delivered, and an impromptu public lecture on the OPERA superluminal neutrino result by the former project manager of OPERA (this was the first official OPERA talk on the subject in North America). The workshop scientific agenda can be viewed at http://www.cpe.vt.edu/snac/program.html. Emerging out of the workshop discussions, was the idea to write a comprehensive white paper describing the current state of the light sterile neutrino. This effort soon became an international collaboration. The final document, titled “Light Sterile Neutrinos: A White Paper” has nearly 200 authors, is 267 pages long, and cites 730 unique references. It has been posted the preprint archive as arXiv:1204.5379 [hep-ph]. Workshop local organizing committee co-chairs, Patrick Huber and Jonathan Link, are the white paper’s head editors. The white paper’s sections and section editors are as follows: 1. Theory and Motivation (Gabriela Barenboim, Valencia and Werner Rodejohann, MPI Heidelberg) 2. Astrophysical Evidence (Kev Abazajian, UC Irvine and Yvonne Wong, Aachen) 3. Evidence from Oscillation Experiments (Joachim Kopp, FNAL and Bill Louis, LANL) 4. Global Picture (Thierry Lasserre, CEA Saclay and Thomas Schwetz, MPI Heidelberg) 5. Requirements for Future Measurements (Bonnie Fleming, Yale and Joe Formaggio, MIT) 6. Appendix: Possible Future Experiments (Patrick Huber, Virginia Tech and Jon Link, Virginia Tech) In all 56 people participated in the workshop, of these 11 were young scientists. The workshop was covered in a feature article in Science (Science, 334, (2011), 304-306.). The DOE award was spent, as budgeted, as contractual services to VT CPE, which is the unit within the University

  11. (11)C-Methionine uptake in secondary brain epilepsy.

    PubMed

    Lopci, E; Bello, L; Chiti, A

    2014-01-01

    Carbon-11 methionine ((11)C-Methionine) is a radio-labeled amino acid currently utilized in Positron Emission Tomography (PET) for imaging primary and metastatic brain tumors. Its clinical use relies mostly on oncologic applications, but the tracer has the potential to investigate other non-malignant conditions. So far, very limited evidence concerns the use of (11)C-Methionine in patients suffering from seizure; however, the tracer can find a proper utilization in this setting especially as a diagnostic complement to (18)F-Fluorodeoxyglucose ((18)F-FDG). Herein we report the case of a 57-year-old patient presenting with epileptic crises secondary to a brain metastasis from bladder carcinoma, who was investigated in our institution with (11)C-Methionine PET. The scan documented the disease recurrence in the left parietal lobe associated with a diffused tracer uptake in the surrounding cerebral circumvolutions, derived from the comitial status. After surgical removal of the metastatic lesion, the patient experienced a complete recovery of symptoms and no further onset of secondary seizure.

  12. Melting Behaviour of Carbonated MORB: the transition zone carbon filter

    NASA Astrophysics Data System (ADS)

    Thomson, A. R.; Walter, M. J.; Kohn, S. C.

    2014-12-01

    ledge may act as a carbon filter for downgoing slabs, and might be responsible for some low velocity anomalies seen above the 410 km seismic discontinuity. [1] Maruyama & Okamoto (2007) Gond Res 11, 148-165. [2] Martin and Hammouda (2011) Eur J Min 23, 5-16. [3] Syracuse et al. (2010) Phys Earth Plan Int 183, 73-90.

  13. Slc4a11 Gene Disruption in Mice

    PubMed Central

    Lopez, Ivan A.; Rosenblatt, Mark I.; Kim, Charles; Galbraith, Gary C.; Jones, Sherri M.; Kao, Liyo; Newman, Debra; Liu, Weixin; Yeh, Stacey; Pushkin, Alexander; Abuladze, Natalia; Kurtz, Ira

    2009-01-01

    NaBC1 (the SLC4A11 gene) belongs to the SLC4 family of sodium-coupled bicarbonate (carbonate) transporter proteins and functions as an electrogenic sodium borate cotransporter. Mutations in SLC4A11 cause either corneal abnormalities (corneal hereditary dystrophy type 2) or a combined auditory and visual impairment (Harboyan syndrome). The role of NaBC1 in sensory systems is poorly understood, given the difficulty of studying patients with NaBC1 mutations. We report our findings in Slc4a11−/− mice generated to investigate the role of NaBC1 in sensorineural systems. In wild-type mice, specific NaBC1 immunoreactivity was detected in fibrocytes of the spiral ligament, from the basal to the apical portion of the cochlea. NaBC1 immunoreactivity was present in the vestibular labyrinth, in stromal cells underneath the non-immunoreactive sensory epithelia of the macula utricle, sacule, and crista ampullaris, and the membranous vestibular labyrinth was collapsed. Both auditory brain response and vestibular evoked potential waveforms were significantly abnormal in Slc4a11−/− mice. In the cornea, NaBC1 was highly expressed in the endothelial cell layer with less staining in epithelial cells. However, unlike humans, the corneal phenotype was mild with a normal slit lamp evaluation. Corneal endothelial cells were morphologically normal; however, both the absolute height of the corneal basal epithelial cells and the relative basal epithelial cell/total corneal thickness were significantly increased in Slc4a11−/− mice. Our results demonstrate for the first time the importance of NaBC1 in the audio-vestibular system and provide support for the hypothesis that SLC4A11 should be considered a potential candidate gene in patients with isolated sensorineural vestibular hearing abnormalities. PMID:19586905

  14. Protolytic carbon film technology

    SciTech Connect

    Renschler, C.L.; White, C.A.

    1996-04-01

    This paper presents a technique for the deposition of polyacrylonitrile (PAN) on virtually any surface allowing carbon film formation with only the caveat that the substrate must withstand carbonization temperatures of at least 600 degrees centigrade. The influence of processing conditions upon the structure and properties of the carbonized film is discussed. Electrical conductivity, microstructure, and morphology control are also described.

  15. Intro to Carbon Sequestration

    ScienceCinema

    None

    2016-07-12

    NETL's Carbon Sequestration Program is helping to develop technologies to capture, purify, and store carbon dioxide (CO2) in order to reduce greenhouse gas emissions without adversely influencing energy use or hindering economic growth. Carbon sequestration technologies capture and store CO2 that would otherwise reside in the atmosphere for long periods of time.

  16. Carbon Goes To…

    ERIC Educational Resources Information Center

    Savasci, Funda

    2014-01-01

    The purposes of this activity are to help middle school students understand the carbon cycle and realize how human activities affect the carbon cycle. This activity consists of two parts. The first part of the activity focuses on the carbon cycle, especially before the Industrial Revolution, while the second part of the activity focuses on how…

  17. Intro to Carbon Sequestration

    SciTech Connect

    2008-03-06

    NETL's Carbon Sequestration Program is helping to develop technologies to capture, purify, and store carbon dioxide (CO2) in order to reduce greenhouse gas emissions without adversely influencing energy use or hindering economic growth. Carbon sequestration technologies capture and store CO2 that would otherwise reside in the atmosphere for long periods of time.

  18. Carbon/Carbon Pistons for Internal Combustion Engines

    NASA Technical Reports Server (NTRS)

    Taylor, A. H.

    1986-01-01

    Carbon/carbon piston performs same function as aluminum pistons in reciprocating internal combustion engines while reducing weight and increasing mechanical and thermal efficiencies of engine. Carbon/carbon piston concept features low piston-to-cylinder wall clearance - so low piston rings and skirts unnecessary. Advantages possible by negligible coefficient of thermal expansion of carbon/carbon.

  19. Ocean sciences after September 11

    NASA Astrophysics Data System (ADS)

    McPhaden, Michael J.

    The terrorist attacks in New York City and Washington D.C. on September 11, 2001 shocked the world with their audacity and destruction. Shortly thereafter, bioterrorists struck through the U.S. postal system. Virtually overnight, major policy shifts took place in the United States that catapulted national security and homeland defense to the top of the political agenda. The consequences were unimaginable just a few months before: an international coalition at war against the Taliban in Afghanistan, major increases in U.S. defense spending, tightened security measures at airports, government facilities, and research laboratories, and a new sense of vulnerability in the post-cold war era. AGU itself was directly affected: three of its members perished in the hijacked planes, or on the ground in New York City.

  20. The Apollo 11 Prime Crew

    NASA Technical Reports Server (NTRS)

    1969-01-01

    Portrait of the prime crew of the Apollo 11 lunar landing mission. From left to right they are: Commander, Neil A. Armstrong, Command Module Pilot, Michael Collins, and Lunar Module Pilot, Edwin E. Aldrin Jr. On July 20th 1969 at 4:18 PM, EDT the Lunar Module 'Eagle' landed in a region of the Moon called the Mare Tranquillitatis, also known as the Sea of Tranquillity. After securing his spacecraft, Armstrong radioed back to earth: 'Houston, Tranquility Base here, the Eagle has landed'. At 10:56 p.m. that same evening and witnessed by a worldwide television audience, Neil Armstrong stepped off the 'Eagle's landing pad onto the lunar surface and said: 'That's one small step for a man, one giant leap for mankind.' He became the first human to set foot upon the Moon.

  1. High-pressure vapor-liquid equilibria of two binary systems: Carbon dioxide + cyclohexanol and carbon dioxide + cyclohexanone

    SciTech Connect

    Laugier, S.; Richon, D.

    1997-01-01

    Vapor-liquid equilibria for carbon dioxide + cyclohexanol and carbon dioxide + cyclohexanone were measured using an apparatus based on a static-analytic method with in situ samplings. P, T, x, y measurements were made at pressures up to 22 MPa. The carbon dioxide + cyclohexanol system was studied at 433 and 473 K, and carbon dioxide + cyclohexanone, at 433 and 473 K. The results are correlated by the Redlich-Kwong-Soave and Peng and Robinson equations and several mixing rules. The best fittings are obtained with the Peng-Robinson equation of state and a two-parameter mixing rule, i.e., within 1.1% for both pressures and vapor mole fractions on the carbon dioxide + cyclohexanone system and within 1.9% for pressures and 2.9% for vapor mole fractions on the carbon dioxide + cyclohexanol system. More recent equations by Patel and Teja and Salim and Trebble show no significant advantages.

  2. Carbon monoxide in rainwater.

    PubMed

    Swinnerton, J W; Lamontagne, R A; Linnenbom, V J

    1971-05-28

    Concentrations of carbon monoxide in rainwater collected at widely diverse locations show up to a 200-fold supersaturation relative to the partial pressure of the gas in the atmosphere. These results indicate the existence of an additional natural source of carbon monoxide not heretofore considered. Production of carbon monoxide in clouds is tentatively attributed to the photochemical oxidation of organic matter or the slight dissociation of carbon dioxide induced by electrical discharges, or both. Methane concentrations measured in the same rainwater show that the partitioning of this gas, unlike that of carbon monoxide, is very close to a state of equilibrium.

  3. Nonmagnetic carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Lipert, Kamil; Kretzschmar, Florian; Ritschel, Manfred; Leonhardt, Albrecht; Klingeler, Rüdiger; Büchner, Bernd

    2009-03-01

    We have synthesized by chemical vapor deposition (CVD) single-, double-, and multiwalled carbon nanotubes without magnetic impurities. In particular, we have applied a rhenium-based CVD technique yielding nonmagnetic carbon nanotubes with diamagnetic Re particles. In addition, carbon nanotubes prepared with iron as catalyst particles are annealed at very high temperatures in which the catalyst material is completely vaporized, while the carbon nanotubes are structurally preserved. Detailed magnetic studies show for both approaches a clear diamagnetic behavior typical for pure carbon nanotubes but no indication of ferromagnetic or paramagnetic material.

  4. 40 CFR 600.115-11 - Criteria for determining the fuel economy label calculation method.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... VEHICLES Fuel Economy and Carbon-Related Exhaust Emission Test Procedures § 600.115-11 Criteria for... derived 5-cycle method for determining fuel economy label values, as specified in § 600.210-08(a)(2) or (b... economy label values must be determined according to the vehicle-specific 5-cycle method specified...

  5. Evaluation of [11C]metergoline as a PET radiotracer for 5HTR in nonhuman primates

    SciTech Connect

    Hooker, J.M.; Hooker, J.M.; Kim, S.W.; Reibel, A.T.; Alexoff, D.; Xu, Y.; Shea, C.

    2010-04-20

    Metergoline, a serotonin receptor antagonist, was labeled with carbon-11 in order to evaluate its pharmacokinetics and distribution in non-human primates using positron emission tomography. [{sup 11}C]Metergoline had moderate brain uptake and exhibited heterogeneous specific binding, which was blocked by pretreatment with metergoline and altanserin throughout the cortex. Non-specific binding and insensitivity to changes in synaptic serotonin limit its potential as a PET radiotracer. However, the characterization of [{sup 11}C]metergoline pharmacokinetics and binding in the brain and peripheral organs using PET improves our understanding of metergoline drug pharmacology.

  6. Inorganic carbon speciation and fluxes in the Congo River

    NASA Astrophysics Data System (ADS)

    Wang, Zhaohui Aleck; Bienvenu, Dinga Jean; Mann, Paul J.; Hoering, Katherine A.; Poulsen, John R.; Spencer, Robert G. M.; Holmes, Robert M.

    2013-02-01

    Seasonal variations in inorganic carbon chemistry and associated fluxes from the Congo River were investigated at Brazzaville-Kinshasa. Small seasonal variation in dissolved inorganic carbon (DIC) was found in contrast with discharge-correlated changes in pH, total alkalinity (TA), carbonate species, and dissolved organic carbon (DOC). DIC was almost always greater than TA due to the importance of CO2*, the sum of dissolved CO2 and carbonic acid, as a result of low pH. Organic acids in DOC contributed 11-61% of TA and had a strong titration effect on water pH and carbonate speciation. The CO2* and bicarbonate fluxes accounted for ~57% and 43% of the DIC flux, respectively. Congo River surface water released CO2 at a rate of ~109 mol m-2 yr-1. The basin-wide DIC yield was ~8.84 × 104 mol km-2 yr-1. The discharge normalized DIC flux to the ocean amounted to 3.11 × 1011 mol yr-1. The DOC titration effect on the inorganic carbon system may also be important on a global scale for regulating carbon fluxes in rivers.

  7. A comparison of black carbon measurement methods for combustion sources

    NASA Astrophysics Data System (ADS)

    Holder, A. L.; Pavlovic, J.; Yelverton, T.; Hagler, G.; Aurell, J.; Ebersviller, S.; Seay, B.; Jetter, J.; Gullett, B.; Hays, M. D.

    2015-12-01

    Black carbon is an important short-term climate forcer that has been linked with adverse health effects. Multiple black carbon measurement methodologies exist, but no standard measurement method or calibration material has been agreed upon. Moreover, the U.S. Environmental Protection Agency uses elemental carbon in its ambient monitoring networks and in its emissions inventory, assuming that elemental carbon is equivalent to black carbon. Instrument comparisons with ambient aerosols have demonstrated considerable differences between black carbon and elemental carbon, as well as among different black carbon measurements. However, there have been few published comparable studies for source emissions. We used multiple measurement methods to quantify black carbon and elemental carbon emissions from a range of combustion sources (diesel gensets, coal fired boilers, prescribed fires and cookstoves) emitting particles of varying composition and physical characteristics. The ratio of black carbon to elemental carbon (BC/EC) ranged from 0.50 to 2.8 and depended upon the combustion source. The greatest agreement was observed for emissions from cookstoves (BC/EC = 1.1 ± 0.3). The largest differences were seen for emissions from large stationary diesel genset (BC/EC = 2.3 ± 0.5) and were most pronounced when a diesel particulate filter was used (BC/EC 2.5 ± 0.6). This suggests that this source category may be underrepresented in emissions inventories based on elemental carbon. Black carbon concentrations derived from filter-based attenuation were highly correlated with photo-acoustic absorption measurements, but were generally 50% greater. This is likely due to the choice of calibration factor, which is currently ambiguously defined. These results highlight the importance of developing a standard calibration material to improve comparability among measurements.

  8. On Carbon Burning in Super Asymptotic Giant Branch Stars

    NASA Astrophysics Data System (ADS)

    Farmer, R.; Fields, C. E.; Timmes, F. X.

    2015-07-01

    We explore the detailed and broad properties of carbon burning in Super Asymptotic Giant Branch (SAGB) stars with 2755 MESA stellar evolution models. The location of first carbon ignition, quenching location of the carbon-burning flames and flashes, angular frequency of the carbon core, and carbon core mass are studied as a function of the zero-age main sequence (ZAMS) mass, initial rotation rate, and mixing parameters such as convective overshoot, semiconvection, thermohaline, and angular momentum transport. In general terms, we find that these properties of carbon burning in SAGB models are not a strong function of the initial rotation profile, but are a sensitive function of the overshoot parameter. We quasi-analytically derive an approximate ignition density, ρign ≈ 2.1 × 106 g cm-3, to predict the location of first carbon ignition in models that ignite carbon off-center. We also find that overshoot moves the ZAMS mass boundaries where off-center carbon ignition occurs at a nearly uniform rate of ΔMZAMS/Δfov ≈ 1.6 {M}⊙ . For zero overshoot, fov = 0.0, our models in the ZAMS mass range ≈8.9-11 {M}⊙ show off-center carbon ignition. For canonical amounts of overshooting, fov = 0.016, the off-center carbon ignition range shifts to ≈7.2-8.8 {M}⊙ . Only systems with fov ≥ 0.01 and ZAMS mass ≈7.2-8.0 {M}⊙ show carbon burning is quenched a significant distance from the center. These results suggest a careful assessment of overshoot modeling approximations on claims that carbon burning quenches an appreciable distance from the center of the carbon core.

  9. Mechanisms of soil carbon storage in experimental grasslands

    NASA Astrophysics Data System (ADS)

    Steinbeiss, S.; Temperton, V. M.; Gleixner, G.

    2007-10-01

    We investigated the fate of root and litter derived carbon into soil organic matter and dissolved organic matter in soil profiles, in order to explain unexpected positive effects of plant diversity on carbon storage. A time series of soil and soil solution samples was investigated at the field site of The Jena Experiment. In addition to the main biodiversity experiment with C3 plants, a C4 species (Amaranthus retroflexus L.) naturally labeled with 13C was grown on an extra plot. Changes in organic carbon concentration in soil and soil solution were combined with stable isotope measurements to follow the fate of plant carbon into the soil and soil solution. A split plot design with plant litter removal versus double litter input simulated differences in biomass input. After 2 years, the no litter and double litter treatment, respectively, showed an increase of 381 g C m-2 and 263 g C m-2 to 20 cm depth, while 71 g C m-2 and 393 g C m-2 were lost between 20 and 30 cm depth. The isotopic label in the top 5 cm indicated that 11 and 15% of soil organic carbon were derived from plant material on the no litter and the double litter treatment, respectively. Without litter, this equals the total amount of carbon newly stored in soil, whereas with double litter this corresponds to twice the amount of stored carbon. Our results indicate that litter input resulted in lower carbon storage and larger carbon losses and consequently accelerated turnover of soil organic carbon. Isotopic evidence showed that inherited soil organic carbon was replaced by fresh plant carbon near the soil surface. Our results suggest that primarily carbon released from soil organic matter, not newly introduced plant organic matter, was transported in the soil solution and contributed to the observed carbon storage in deeper horizons.

  10. Characteristics of permeability in carbonate areas of Korea

    NASA Astrophysics Data System (ADS)

    Park, Y.; Lee, J.; Lim, H.; Keehm, Y.

    2010-12-01

    Permeability (hydraulic conductivity) in carbonate areas is affected by various factors such as fracture, pore and degree of weathering and diagenesis. Also, caves developed in carbonate area are main factors. This study was performed to understand factors controlling the permeability in carbonate areas in Korea. In order to conduct this study, the permeability and well logging data (n=30) were collected from many literatures and rock samples were collected around wells. Vertical profile of the carbonate areas can be classified into soil, weathered carbonate and fresh carbonate zone. They show a different range at each region. Most of the rock samples were hardly weathered. The permeability showed wide ranges (0.009 to 1.1 m/day). The average value of the permeability was 0.159 m/day. However, 80% (n=24) of total data had the permeability valves lower than 0.1 m/day. The permeability values were distinguished according to degree of development of fractures. The permeability showed low values (approximately <0.04 m/day) in hardly fractured carbonate area, intermediate values (approximately 0.04 to 0.5 m/day) in fractured carbonate area and high values (approximately >0.5 m/day) in highly fractured carbonate. These results mean that fractures are dominant factors controlling the permeability in carbonate areas of Korea than others. This work was supported by Energy Resource R&D program (2009T100200058) under the Ministry of Knowledge Economy, Republic of Korea.

  11. Perturbations in the carbon budget of the tropics

    PubMed Central

    Grace, John; Mitchard, Edward; Gloor, Emanuel

    2014-01-01

    The carbon budget of the tropics has been perturbed as a result of human influences. Here, we attempt to construct a ‘bottom-up’ analysis of the biological components of the budget as they are affected by human activities. There are major uncertainties in the extent and carbon content of different vegetation types, the rates of land-use change and forest degradation, but recent developments in satellite remote sensing have gone far towards reducing these uncertainties. Stocks of carbon as biomass in tropical forests and woodlands add up to 271 ± 16 Pg with an even greater quantity of carbon as soil organic matter. Carbon loss from deforestation, degradation, harvesting and peat fires is estimated as 2.01 ± 1.1 Pg annum−1; while carbon gain from forest and woodland growth is 1.85 ± 0.09 Pg annum−1. We conclude that tropical lands are on average a small carbon source to the atmosphere, a result that is consistent with the ‘top-down’ result from measurements in the atmosphere. If they were to be conserved, they would be a substantial carbon sink. Release of carbon as carbon dioxide from fossil fuel burning in the tropics is 0.74 Pg annum−1 or 0.57 MgC person−1 annum−1, much lower than the corresponding figures from developed regions of the world. PMID:24902948

  12. Perturbations in the carbon budget of the tropics.

    PubMed

    Grace, John; Mitchard, Edward; Gloor, Emanuel

    2014-10-01

    The carbon budget of the tropics has been perturbed as a result of human influences. Here, we attempt to construct a 'bottom-up' analysis of the biological components of the budget as they are affected by human activities. There are major uncertainties in the extent and carbon content of different vegetation types, the rates of land-use change and forest degradation, but recent developments in satellite remote sensing have gone far towards reducing these uncertainties. Stocks of carbon as biomass in tropical forests and woodlands add up to 271 ± 16 Pg with an even greater quantity of carbon as soil organic matter. Carbon loss from deforestation, degradation, harvesting and peat fires is estimated as 2.01 ± 1.1 Pg annum(-1); while carbon gain from forest and woodland growth is 1.85 ± 0.09 Pg annum(-1). We conclude that tropical lands are on average a small carbon source to the atmosphere, a result that is consistent with the 'top-down' result from measurements in the atmosphere. If they were to be conserved, they would be a substantial carbon sink. Release of carbon as carbon dioxide from fossil fuel burning in the tropics is 0.74 Pg annum(-1) or 0.57 MgC person(-1) annum(-1) , much lower than the corresponding figures from developed regions of the world.

  13. Double layer capacitance of carbon foam electrodes

    SciTech Connect

    Delnick, F.M.; Ingersoll, D.; Firsich, D.

    1993-11-01

    We have evaluated a wide variety of microcellular carbon foams prepared by the controlled pyrolysis and carbonization of several polymers including: polyacrylonitrile (PAN), polymethacrylonitrile (PMAN), resorcinol/formaldehyde (RF), divinylbenzene/methacrylonitrile (DVB), phenolics (furfuryl/alcohol), and cellulose polymers such as Rayon. The porosity may be established by several processes including: Gelation (1-5), phase separation (1-3,5-8), emulsion (1,9,10), aerogel/xerogel formation (1,11,12,13), replication (14) and activation. In this report we present the complex impedance analysis and double layer charging characteristics of electrodes prepared from one of these materials for double layer capacitor applications, namely activated cellulose derived microcellular carbon foam.

  14. CARBON STARS WITH INFRARED SPECTRA IN GROUP P OF THE IRAS/LRS DATABASE

    SciTech Connect

    Chen, P. S.

    2012-10-01

    Sources with infrared spectra in Group P of the IRAS/LRS database all show polycyclic aromatic hydrocarbon features. They are often planetary nebulae, H II regions, reflection/dark nebulae, Wolf-Rayet stars, or external galaxies. However, we noted that some carbon stars are also included in this group. We searched for and investigated all infrared spectra in Group P of the IRAS/LRS database. Finally, we found 11 previously known carbon stars and identified 8 new candidate carbon stars in Group P. Infrared spectra of these stars may present the 11.2 {mu}m SiC emission features indicative of their carbon-rich properties.

  15. Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

    SciTech Connect

    O'Connor, W.K.; Dahlin, D.C.; Nilsen, D.N.; Walters, R.P.; Turner, P.C.

    2000-07-01

    The Albany Research Center (ARC) of the US Department of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite and member (mg{sub 2}SiO{sub 4})], or serpentine [Mg{sub 3}Si{sub 2}O{sub 5}(OH){sub 4}]. This slurry is reacted with supercritical carbon dioxide (CO{sub 2}) to produce magnesite (MgCO{sub 3}). The CO{sub 2} is dissolved in water to form carbonic acid (H{sub 2}CO{sub 3}), which dissociates to H{sup +} and HCO{sub 3}{sup {minus}}. The H{sup +} reacts with the mineral, liberating Mg{sup 2+} cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO{sub 2} pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185 C and a partial pressure of CO{sub 2} (P{sub CO{sub 2}}) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction conditions, have achieved roughly 83% conversion of heat treated serpentine

  16. Carbon dioxide sequestration by direct mineral carbonation with carbonic acid

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Nilsen, David N.; Walters, Richard P.; Turner, Paul C.

    2000-01-01

    The Albany Research Center (ARC) of the U.S. Dept. of Energy (DOE) has been conducting a series of mineral carbonation tests at its Albany, Oregon, facility over the past 2 years as part of a Mineral Carbonation Study Program within the DOE. Other participants in this Program include the Los Alamos National Laboratory, Arizona State University, Science Applications International Corporation, and the DOE National Energy Technology Laboratory. The ARC tests have focused on ex-situ mineral carbonation in an aqueous system. The process developed at ARC utilizes a slurry of water mixed with a magnesium silicate mineral, olivine [forsterite end member (Mg2SiO4)], or serpentine [Mg3Si2O5(OH)4]. This slurry is reacted with supercritical carbon dioxide (CO2) to produce magnesite (MgCO3). The CO2 is dissolved in water to form carbonic acid (H2CO3), which dissociates to H+ and HCO3 -. The H+ reacts with the mineral, liberating Mg2+ cations which react with the bicarbonate to form the solid carbonate. The process is designed to simulate the natural serpentinization reaction of ultramafic minerals, and for this reason, these results may also be applicable to in-situ geological sequestration regimes. Results of the baseline tests, conducted on ground products of the natural minerals, have been encouraging. Tests conducted at ambient temperature (22 C) and subcritical CO2 pressures (below 73 atm) resulted in very slow conversion to the carbonate. However, when elevated temperatures and pressures are utilized, coupled with continuous stirring of the slurry and gas dispersion within the water column, significant reaction occurs within much shorter reaction times. Extent of reaction, as measured by the stoichiometric conversion of the silicate mineral (olivine) to the carbonate, is roughly 90% within 24 hours, using distilled water, and a reaction temperature of 185?C and a partial pressure of CO2 (PCO2) of 115 atm. Recent tests using a bicarbonate solution, under identical reaction

  17. 11 CFR 109.11 - When is a “non-authorization notice” (disclaimer) required?

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... requirements of 11 CFR 110.11. ... 11 Federal Elections 1 2010-01-01 2010-01-01 false When is a ânon-authorization noticeâ (disclaimer) required? 109.11 Section 109.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL...

  18. 11 CFR 109.11 - When is a “non-authorization notice” (disclaimer) required?

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... requirements of 11 CFR 110.11. ... 11 Federal Elections 1 2012-01-01 2012-01-01 false When is a ânon-authorization noticeâ (disclaimer) required? 109.11 Section 109.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL...

  19. 11 CFR 109.11 - When is a “non-authorization notice” (disclaimer) required?

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... requirements of 11 CFR 110.11. ... 11 Federal Elections 1 2011-01-01 2011-01-01 false When is a ânon-authorization noticeâ (disclaimer) required? 109.11 Section 109.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL...

  20. 11 CFR 109.11 - When is a “non-authorization notice” (disclaimer) required?

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... requirements of 11 CFR 110.11. ... 11 Federal Elections 1 2014-01-01 2014-01-01 false When is a ânon-authorization noticeâ (disclaimer) required? 109.11 Section 109.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL...

  1. 11 CFR 109.11 - When is a “non-authorization notice” (disclaimer) required?

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... defeat of a clearly identified candidate, such person shall comply with the requirements of 11 CFR 110.11. ... 11 Federal Elections 1 2013-01-01 2012-01-01 true When is a ânon-authorization noticeâ (disclaimer) required? 109.11 Section 109.11 Federal Elections FEDERAL ELECTION COMMISSION GENERAL COORDINATED...

  2. Assessing variability in belowground carbon for CMIP-5 models

    NASA Astrophysics Data System (ADS)

    Todd-Brown, K. E.; Hoffman, F. M.; Randerson, J. T.; Post, W. M.; Allison, S. D.

    2011-12-01

    Soil carbon stocks and heterotrophic respiration are critical components of the global carbon cycle. This study compared soil carbon survey data with modeled stocks and assessed the magnitude of change in modeled soil carbon between 1850 and 2005. Model means (1995-2005) from the CMIP-5 historical experiment were compared to soil carbon estimates from the Harmonized World Soil Database (HWSD) across biomes derived from the MODIS/Terra+Aqua land cover type. Changes in soil carbon stocks were calculated as the difference between the 1850-1860 and 1995-2005 model means. In general, the models overestimated modern soil carbon stocks in areas of relatively low soil carbon (<100 kg m^-2) by 310 Pg (28%) and underestimated modern soil carbon stocks in areas of relatively high soil carbon (>100 kg m^-2) by 1012 Pg (85%) (n=7). Total modern soil carbon ranged from 1120-2523 Pg among the models versus 2280 Pg from the HWSD. These results imply that the models do not represent the high soil carbon of peatlands well. Models underestimated soil carbon in the boreal forest by 417 Pg (61%) (sd=47, cv=0.11, n=7). Soil carbon predictions for temperate forests were closest to HWSD with an overestimate of 13 Pg (21%) (sd=13, cv=0.96, n=7). Over the course of the simulations, average model soil carbon stocks increased 6% gobally (sd=4, cv=0.65, n=7) from 1563 Pg to 1664 Pg. This change was accompanied by a 22% (sd=5, cv=0.26, n=4) increase in modeled NPP from 73 Pg-C/yr to 89 Pg-C/yr for models that report NPP. In summary, the CMIP5 models tend to underestimate total soil carbon stocks, particularly in areas with high soil carbon concentration. Despite rising temperatures over the past 150 years, these models also predicted a substantial increase in soil carbon stocks that is likely due to increased NPP. Whether this rate of increase can be verified with empirical data or sustained over the 21st century is unclear. Given the discrepancies between modeled and observed distributions of

  3. Process of making carbon-carbon composites

    NASA Technical Reports Server (NTRS)

    Withers, James C. (Inventor); Loutfy, Raouf O. (Inventor); Kowbel, Witold (Inventor); Bruce, Calvin (Inventor); Vaidyanathan, Ranji (Inventor)

    2000-01-01

    A carbon composite structure, for example, an automotive engine piston, is made by preparing a matrix including of a mixture of non crystalline carbon particulate soluble in an organic solvent and a binder that has a liquid phase. The non crystalline particulate also contains residual carbon hydrogen bonding. An uncured structure is formed by combining the matrix mixture, for example, carbon fibers such as graphite dispersed in the mixture and/or graphite cloth imbedded in the mixture. The uncured structure is cured by pyrolyzing it in an inert atmosphere such as argon. Advantageously, the graphite reinforcement material is whiskered prior to combining it with the matrix mixture by a novel method involving passing a gaseous metal suboxide over the graphite surface.

  4. 40 CFR 63.993 - Absorbers, condensers, carbon adsorbers and other recovery devices used as final recovery devices.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... flow for each regeneration cycle; and a carbon-bed temperature monitoring device, capable of recording... 40 Protection of Environment 11 2013-07-01 2013-07-01 false Absorbers, condensers, carbon... Absorbers, condensers, carbon adsorbers and other recovery devices used as final recovery devices. (a)...

  5. 11 CFR 9031.1 - Scope.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... FEDERAL ELECTION COMMISSION PRESIDENTIAL ELECTION CAMPAIGN FUND: PRESIDENTIAL PRIMARY MATCHING FUND SCOPE... title 2, United States Code, and regulations prescribed thereunder (11 CFR part 100 through 300). Unless... prescribed thereunder (11 CFR parts 100 through 300)....

  6. 11 CFR 9031.1 - Scope.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... FEDERAL ELECTION COMMISSION PRESIDENTIAL ELECTION CAMPAIGN FUND: PRESIDENTIAL PRIMARY MATCHING FUND SCOPE... title 2, United States Code, and regulations prescribed thereunder (11 CFR part 100 through 300). Unless... prescribed thereunder (11 CFR parts 100 through 300)....

  7. 18 CFR 801.11 - Public values.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... Section 801.11 Conservation of Power and Water Resources SUSQUEHANNA RIVER BASIN COMMISSION GENERAL POLICIES § 801.11 Public values. (a) The basin has many points of archeological and historic interest, and... affecting these attributes of the basin....

  8. 18 CFR 801.11 - Public values.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... Section 801.11 Conservation of Power and Water Resources SUSQUEHANNA RIVER BASIN COMMISSION GENERAL POLICIES § 801.11 Public values. (a) The basin has many points of archeological and historic interest, and... affecting these attributes of the basin....

  9. Genetics Home Reference: spastic paraplegia type 11

    MedlinePlus

    ... with mental impairment and thin corpus callosum HSP-TCC SPG11-related hereditary spastic paraplegia with thin corpus ... A, Stevanin G, Santorelli FM. Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and ...

  10. Mechanical behavior of carbon-carbon composites

    NASA Technical Reports Server (NTRS)

    Rozak, G. A.

    1984-01-01

    A general background, test plan, and some results of preliminary examinations of a carbon-carbon composite material are presented with emphasis on mechanical testing and inspection techniques. Experience with testing and evaluation was gained through tests of a low modulus carbon-carbon material, K-Karb C. The properties examined are the density - 1.55 g/cc; four point flexure strength in the warp - 137 MPa (19,800 psi) and the fill - 95.1 MPa (13,800 psi,) directions; and the warp interlaminar shear strength - 14.5 MPa (2100 psi). Radiographic evaluation revealed thickness variations and the thinner areas of the composite were scrapped. The ultrasonic C-scan showed attenuation variations, but these did not correspond to any of the physical and mechanical properties measured. Based on these initial tests and a survey of the literature, a plan has been devised to examine the effect of stress on the oxidation behavior, and the strength degradation of coated carbon-carbon composites. This plan will focus on static fatigue tests in the four point flexure mode in an elevated temperature, oxidizing environment.

  11. Cadherin-11 endocytosis through binding to clathrin promotes cadherin-11-mediated migration in prostate cancer cells.

    PubMed

    Satcher, Robert L; Pan, Tianhong; Bilen, Mehmet A; Li, Xiaoxia; Lee, Yu-Chen; Ortiz, Angelica; Kowalczyk, Andrew P; Yu-Lee, Li-Yuan; Lin, Sue-Hwa

    2015-12-15

    Cadherin-11 (Cad11) cell adhesion molecule plays a role in prostate cancer cell migration. Because disassembly of adhesion complexes through endocytosis of adhesion proteins has been shown to play a role in cell migration, we examined whether Cad11 endocytosis plays a role in Cad11-mediated migration. The mechanism by which Cad11 is internalized is unknown. Using a GST pulldown assay, we found that clathrin binds to the Cad11 cytoplasmic domain but not to that of E-cadherin. Using deletion analysis, we identified a unique sequence motif, VFEEE, in the Cad11 membrane proximal region (amino acid residues 11-15) that binds to clathrin. Endocytosis assays using K(+)-depletion buffer showed that Cad11 internalization is clathrin dependent. Proximity ligation assays showed that Cad11 colocalizes with clathrin, and immunofluorescence assays showed that Cad11 localizes in vesicles that stain for the early endosomal marker Rab5. Deletion of the VFEEE sequence from the Cad11 cytoplasmic domain (Cad11-cla-Δ5) leads to inhibition of Cad11 internalization and reduces Cad11-mediated cell migration in C4-2B and PC3-mm2 prostate cancer cells. These observations suggest that clathrin-mediated internalization of Cad11 regulates surface trafficking of Cad11 and that dynamic turnover of Cad11 regulates the migratory function of Cad11 in prostate cancer cells.

  12. 25 CFR 11.407 - Sexual assault.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... gratifying sexual desire, or for the purpose of abusing, humiliating, harassing, or degrading the victim. ... 25 Indians 1 2010-04-01 2010-04-01 false Sexual assault. 11.407 Section 11.407 Indians BUREAU OF... Criminal Offenses § 11.407 Sexual assault. (a) A person who has sexual contact with another person not...

  13. 25 CFR 11.407 - Sexual assault.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... gratifying sexual desire, or for the purpose of abusing, humiliating, harassing, or degrading the victim. ... 25 Indians 1 2011-04-01 2011-04-01 false Sexual assault. 11.407 Section 11.407 Indians BUREAU OF... Criminal Offenses § 11.407 Sexual assault. (a) A person who has sexual contact with another person not...

  14. 11 CFR 9036.5 - Resubmissions.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... (including the data base for those candidates maintaining their contributor list on computer). (d... the submission review pursuant to 11 CFR 9036.4(b), or of an inquiry pursuant to 11 CFR 9039.3 that... presentation of resubmissions. If the candidate chooses to resubmit any contributions under 11 CFR...

  15. 12 CFR 23.11 - Lease term.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 1 2010-01-01 2010-01-01 false Lease term. 23.11 Section 23.11 Banks and Banking COMPTROLLER OF THE CURRENCY, DEPARTMENT OF THE TREASURY LEASING CEBA Leases § 23.11 Lease term. A CEBA Lease must have an initial term of not less than 90 days. A national bank may acquire...

  16. 25 CFR 11.601 - Marriage licenses.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Marriage licenses. 11.601 Section 11.601 Indians BUREAU... ORDER CODE Domestic Relations § 11.601 Marriage licenses. A marriage license shall be issued by the clerk of the court in the absence of any showing that the proposed marriage would be invalid under...

  17. 25 CFR 11.600 - Marriages.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Marriages. 11.600 Section 11.600 Indians BUREAU OF INDIAN... Domestic Relations § 11.600 Marriages. (a) A magistrate of the Court of Indian Offenses shall have the authority to perform marriages. (b) A valid marriage shall be constituted by: (1) The issuance of a...

  18. 8 CFR 103.11 - Business information.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... accordance with 28 CFR 16.7. ... 8 Aliens and Nationality 1 2010-01-01 2010-01-01 false Business information. 103.11 Section 103.11...; AVAILABILITY OF RECORDS § 103.11 Business information. Business information provided to the Service by...

  19. 37 CFR 11.50 - Evidence.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2012-07-01 2012-07-01 false Evidence. 11.50 Section 11.50... Proceedings; Jurisdiction, Sanctions, Investigations, and Proceedings § 11.50 Evidence. (a) Rules of evidence. The rules of evidence prevailing in courts of law and equity are not controlling in hearings...

  20. 37 CFR 11.50 - Evidence.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2010-07-01 2010-07-01 false Evidence. 11.50 Section 11.50... Proceedings; Jurisdiction, Sanctions, Investigations, and Proceedings § 11.50 Evidence. (a) Rules of evidence. The rules of evidence prevailing in courts of law and equity are not controlling in hearings...

  1. 37 CFR 11.50 - Evidence.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2011-07-01 2011-07-01 false Evidence. 11.50 Section 11.50... Proceedings; Jurisdiction, Sanctions, Investigations, and Proceedings § 11.50 Evidence. (a) Rules of evidence. The rules of evidence prevailing in courts of law and equity are not controlling in hearings...

  2. 37 CFR 11.50 - Evidence.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 37 Patents, Trademarks, and Copyrights 1 2014-07-01 2014-07-01 false Evidence. 11.50 Section 11.50... Proceedings; Jurisdiction, Sanctions, Investigations, and Proceedings § 11.50 Evidence. (a) Rules of evidence. The rules of evidence prevailing in courts of law and equity are not controlling in hearings...

  3. 7 CFR 984.11 - Merchantable walnuts.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 8 2010-01-01 2010-01-01 false Merchantable walnuts. 984.11 Section 984.11... Agreements and Orders; Fruits, Vegetables, Nuts), DEPARTMENT OF AGRICULTURE WALNUTS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 984.11 Merchantable walnuts. (a) Inshell. Merchantable inshell...

  4. 7 CFR 984.11 - Merchantable walnuts.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 7 Agriculture 8 2013-01-01 2013-01-01 false Merchantable walnuts. 984.11 Section 984.11... AGREEMENTS AND ORDERS; FRUITS, VEGETABLES, NUTS), DEPARTMENT OF AGRICULTURE WALNUTS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 984.11 Merchantable walnuts. (a) Inshell. Merchantable inshell...

  5. 7 CFR 984.11 - Merchantable walnuts.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 7 Agriculture 8 2014-01-01 2014-01-01 false Merchantable walnuts. 984.11 Section 984.11... AGREEMENTS AND ORDERS; FRUITS, VEGETABLES, NUTS), DEPARTMENT OF AGRICULTURE WALNUTS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 984.11 Merchantable walnuts. (a) Inshell. Merchantable inshell...

  6. 7 CFR 984.11 - Merchantable walnuts.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 7 Agriculture 8 2012-01-01 2012-01-01 false Merchantable walnuts. 984.11 Section 984.11... Agreements and Orders; Fruits, Vegetables, Nuts), DEPARTMENT OF AGRICULTURE WALNUTS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 984.11 Merchantable walnuts. (a) Inshell. Merchantable inshell...

  7. 7 CFR 984.11 - Merchantable walnuts.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 7 Agriculture 8 2011-01-01 2011-01-01 false Merchantable walnuts. 984.11 Section 984.11... Agreements and Orders; Fruits, Vegetables, Nuts), DEPARTMENT OF AGRICULTURE WALNUTS GROWN IN CALIFORNIA Order Regulating Handling Definitions § 984.11 Merchantable walnuts. (a) Inshell. Merchantable inshell...

  8. 25 CFR 11.454 - Domestic violence.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Domestic violence. 11.454 Section 11.454 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Criminal Offenses § 11.454 Domestic violence. (a) A person who commits domestic violence...

  9. 25 CFR 11.454 - Domestic violence.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 25 Indians 1 2012-04-01 2011-04-01 true Domestic violence. 11.454 Section 11.454 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Criminal Offenses § 11.454 Domestic violence. (a) A person who commits domestic violence by...

  10. 25 CFR 11.454 - Domestic violence.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 25 Indians 1 2014-04-01 2014-04-01 false Domestic violence. 11.454 Section 11.454 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Criminal Offenses § 11.454 Domestic violence. (a) A person who commits domestic violence...

  11. 25 CFR 11.454 - Domestic violence.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 25 Indians 1 2013-04-01 2013-04-01 false Domestic violence. 11.454 Section 11.454 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Criminal Offenses § 11.454 Domestic violence. (a) A person who commits domestic violence...

  12. 25 CFR 11.454 - Domestic violence.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 25 Indians 1 2011-04-01 2011-04-01 false Domestic violence. 11.454 Section 11.454 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Criminal Offenses § 11.454 Domestic violence. (a) A person who commits domestic violence...

  13. 11 CFR 9036.5 - Resubmissions.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... based on that contribution due to the sampling techniques used in reviewing the original submission. (e... the submission review pursuant to 11 CFR 9036.4(b), or of an inquiry pursuant to 11 CFR 9039.3 that... presentation of resubmissions. If the candidate chooses to resubmit any contributions under 11 CFR...

  14. 11 CFR 9036.5 - Resubmissions.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... based on that contribution due to the sampling techniques used in reviewing the original submission. (e... the submission review pursuant to 11 CFR 9036.4(b), or of an inquiry pursuant to 11 CFR 9039.3 that... presentation of resubmissions. If the candidate chooses to resubmit any contributions under 11 CFR...

  15. 11 CFR 9036.5 - Resubmissions.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... based on that contribution due to the sampling techniques used in reviewing the original submission. (e... the submission review pursuant to 11 CFR 9036.4(b), or of an inquiry pursuant to 11 CFR 9039.3 that... presentation of resubmissions. If the candidate chooses to resubmit any contributions under 11 CFR...

  16. 40 CFR 258.11 - Floodplains.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 25 2014-07-01 2014-07-01 false Floodplains. 258.11 Section 258.11... SOLID WASTE LANDFILLS Location Restrictions § 258.11 Floodplains. (a) Owners or operators of new MSWLF units, existing MSWLF units, and lateral expansions located in 100-year floodplains must...

  17. 40 CFR 258.11 - Floodplains.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 26 2013-07-01 2013-07-01 false Floodplains. 258.11 Section 258.11... SOLID WASTE LANDFILLS Location Restrictions § 258.11 Floodplains. (a) Owners or operators of new MSWLF units, existing MSWLF units, and lateral expansions located in 100-year floodplains must...

  18. 40 CFR 258.11 - Floodplains.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 25 2011-07-01 2011-07-01 false Floodplains. 258.11 Section 258.11... SOLID WASTE LANDFILLS Location Restrictions § 258.11 Floodplains. (a) Owners or operators of new MSWLF units, existing MSWLF units, and lateral expansions located in 100-year floodplains must...

  19. 40 CFR 258.11 - Floodplains.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 26 2012-07-01 2011-07-01 true Floodplains. 258.11 Section 258.11... SOLID WASTE LANDFILLS Location Restrictions § 258.11 Floodplains. (a) Owners or operators of new MSWLF units, existing MSWLF units, and lateral expansions located in 100-year floodplains must...

  20. 42 CFR 9.11 - Animal transport.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 42 Public Health 1 2013-10-01 2013-10-01 false Animal transport. 9.11 Section 9.11 Public Health... CHIMPANZEES HELD IN THE FEDERALLY SUPPORTED SANCTUARY SYSTEM § 9.11 Animal transport. The transportation of chimpanzees by surface or air must be in accordance with the requirements set forth in the Animal Welfare...

  1. 42 CFR 9.11 - Animal transport.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 42 Public Health 1 2014-10-01 2014-10-01 false Animal transport. 9.11 Section 9.11 Public Health... CHIMPANZEES HELD IN THE FEDERALLY SUPPORTED SANCTUARY SYSTEM § 9.11 Animal transport. The transportation of chimpanzees by surface or air must be in accordance with the requirements set forth in the Animal Welfare...

  2. 42 CFR 9.11 - Animal transport.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 42 Public Health 1 2012-10-01 2012-10-01 false Animal transport. 9.11 Section 9.11 Public Health... CHIMPANZEES HELD IN THE FEDERALLY SUPPORTED SANCTUARY SYSTEM § 9.11 Animal transport. The transportation of chimpanzees by surface or air must be in accordance with the requirements set forth in the Animal Welfare...

  3. 42 CFR 9.11 - Animal transport.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 42 Public Health 1 2011-10-01 2011-10-01 false Animal transport. 9.11 Section 9.11 Public Health... CHIMPANZEES HELD IN THE FEDERALLY SUPPORTED SANCTUARY SYSTEM § 9.11 Animal transport. The transportation of chimpanzees by surface or air must be in accordance with the requirements set forth in the Animal Welfare...

  4. 30 CFR 48.11 - Hazard training.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 1 2010-07-01 2010-07-01 false Hazard training. 48.11 Section 48.11 Mineral Resources MINE SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR EDUCATION AND TRAINING TRAINING AND RETRAINING OF MINERS Training and Retraining of Underground Miners § 48.11 Hazard training. (a)...

  5. 29 CFR 1604.11 - Sexual harassment.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 4 2011-07-01 2011-07-01 false Sexual harassment. 1604.11 Section 1604.11 Labor... BECAUSE OF SEX § 1604.11 Sexual harassment. (a) Harassment on the basis of sex is a violation of section... physical conduct of a sexual nature constitute sexual harassment when (1) submission to such conduct...

  6. 45 CFR 650.11 - Utilization reports.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 45 Public Welfare 3 2012-10-01 2012-10-01 false Utilization reports. 650.11 Section 650.11 Public Welfare Regulations Relating to Public Welfare (Continued) NATIONAL SCIENCE FOUNDATION PATENTS § 650.11 Utilization reports. Paragraph (h) of the standard Patent Rights clause set forth in § 650.4 obliges...

  7. 45 CFR 650.11 - Utilization reports.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 45 Public Welfare 3 2014-10-01 2014-10-01 false Utilization reports. 650.11 Section 650.11 Public Welfare Regulations Relating to Public Welfare (Continued) NATIONAL SCIENCE FOUNDATION PATENTS § 650.11 Utilization reports. Paragraph (h) of the standard Patent Rights clause set forth in § 650.4 obliges...

  8. 47 CFR 27.11 - Initial authorization.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 47 Telecommunication 2 2012-10-01 2012-10-01 false Initial authorization. 27.11 Section 27.11 Telecommunication FEDERAL COMMUNICATIONS COMMISSION (CONTINUED) COMMON CARRIER SERVICES MISCELLANEOUS WIRELESS COMMUNICATIONS SERVICES Applications and Licenses § 27.11 Initial authorization. (a) An applicant must file...

  9. 47 CFR 27.11 - Initial authorization.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 47 Telecommunication 2 2014-10-01 2014-10-01 false Initial authorization. 27.11 Section 27.11 Telecommunication FEDERAL COMMUNICATIONS COMMISSION (CONTINUED) COMMON CARRIER SERVICES MISCELLANEOUS WIRELESS COMMUNICATIONS SERVICES Applications and Licenses § 27.11 Initial authorization. Link to an amendment...

  10. 47 CFR 27.11 - Initial authorization.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 47 Telecommunication 2 2013-10-01 2013-10-01 false Initial authorization. 27.11 Section 27.11 Telecommunication FEDERAL COMMUNICATIONS COMMISSION (CONTINUED) COMMON CARRIER SERVICES MISCELLANEOUS WIRELESS COMMUNICATIONS SERVICES Applications and Licenses § 27.11 Initial authorization. (a) An applicant must file...

  11. 47 CFR 27.11 - Initial authorization.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 47 Telecommunication 2 2011-10-01 2011-10-01 false Initial authorization. 27.11 Section 27.11 Telecommunication FEDERAL COMMUNICATIONS COMMISSION (CONTINUED) COMMON CARRIER SERVICES MISCELLANEOUS WIRELESS COMMUNICATIONS SERVICES Applications and Licenses § 27.11 Initial authorization. (a) An applicant must file...

  12. 47 CFR 27.11 - Initial authorization.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 47 Telecommunication 2 2010-10-01 2010-10-01 false Initial authorization. 27.11 Section 27.11 Telecommunication FEDERAL COMMUNICATIONS COMMISSION (CONTINUED) COMMON CARRIER SERVICES MISCELLANEOUS WIRELESS COMMUNICATIONS SERVICES Applications and Licenses § 27.11 Initial authorization. (a) An applicant must file...

  13. 16 CFR 1633.11 - Records.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 16 Commercial Practices 2 2010-01-01 2010-01-01 false Records. 1633.11 Section 1633.11 Commercial... (OPEN FLAME) OF MATTRESS SETS Rules and Regulations § 1633.11 Records. (a) Test and manufacturing records C general. Every manufacturer and any other person initially introducing into commerce...

  14. 29 CFR 1912a.11 - Minutes; transcript.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Minutes; transcript. 1912a.11 Section 1912a.11 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED) NATIONAL ADVISORY COMMITTEE ON OCCUPATIONAL SAFETY AND HEALTH § 1912a.11 Minutes; transcript....

  15. 12 CFR 336.11 - Definitions.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 12 Banks and Banking 4 2010-01-01 2010-01-01 false Definitions. 336.11 Section 336.11 Banks and... One-Year Restriction on Post-Employment Activities of Senior Examiners § 336.11 Definitions. For purposes of this subpart: (a) Bank holding company has the meaning given to such term in section 2 of...

  16. 28 CFR 511.11 - Prohibited activities.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Prohibited activities. 511.11 Section 511.11 Judicial Administration BUREAU OF PRISONS, DEPARTMENT OF JUSTICE GENERAL MANAGEMENT AND ADMINISTRATION GENERAL MANAGEMENT POLICY Searching and Detaining or Arresting Non-Inmates § 511.11...

  17. 14 CFR 77.11 - Scope.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 2 2010-01-01 2010-01-01 false Scope. 77.11 Section 77.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIRSPACE OBJECTS AFFECTING NAVIGABLE AIRSPACE Notice of Construction or Alteration § 77.11 Scope. (a) This subpart...

  18. 7 CFR 4284.11 - Award requirements.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 7 Agriculture 15 2010-01-01 2010-01-01 false Award requirements. 4284.11 Section 4284.11 Agriculture Regulations of the Department of Agriculture (Continued) RURAL BUSINESS-COOPERATIVE SERVICE AND... Grant Programs § 4284.11 Award requirements. In addition to specific grant requirements, all...

  19. 25 CFR 11.1010 - Adjudicatory hearing.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 25 Indians 1 2010-04-01 2010-04-01 false Adjudicatory hearing. 11.1010 Section 11.1010 Indians BUREAU OF INDIAN AFFAIRS, DEPARTMENT OF THE INTERIOR LAW AND ORDER COURTS OF INDIAN OFFENSES AND LAW AND ORDER CODE Juvenile Offender Procedure § 11.1010 Adjudicatory hearing. (a) The children's court...

  20. 30 CFR 556.11 - Helium.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false Helium. 556.11 Section 556.11 Mineral Resources... § 556.11 Helium. (a) Each lease issued or continued under these regulations shall be subject to a... helium from all gas produced from the leased area. (b) In case the United States elects to take...

  1. 30 CFR 556.11 - Helium.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false Helium. 556.11 Section 556.11 Mineral Resources... § 556.11 Helium. (a) Each lease issued or continued under these regulations shall be subject to a... helium from all gas produced from the leased area. (b) In case the United States elects to take...

  2. 30 CFR 556.11 - Helium.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false Helium. 556.11 Section 556.11 Mineral Resources... § 556.11 Helium. (a) Each lease issued or continued under these regulations shall be subject to a... helium from all gas produced from the leased area. (b) In case the United States elects to take...

  3. 14 CFR 95.11 - General.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... 14 Aeronautics and Space 2 2011-01-01 2011-01-01 false General. 95.11 Section 95.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR TRAFFIC AND GENERAL OPERATING RULES IFR ALTITUDES Designated Mountainous Areas § 95.11 General. The areas described...

  4. 14 CFR 95.11 - General.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 14 Aeronautics and Space 2 2012-01-01 2012-01-01 false General. 95.11 Section 95.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR TRAFFIC AND GENERAL OPERATING RULES IFR ALTITUDES Designated Mountainous Areas § 95.11 General. The areas described...

  5. 14 CFR 95.11 - General.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 14 Aeronautics and Space 2 2014-01-01 2014-01-01 false General. 95.11 Section 95.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR TRAFFIC AND GENERAL OPERATING RULES IFR ALTITUDES Designated Mountainous Areas § 95.11 General. The areas described...

  6. 14 CFR 95.11 - General.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 14 Aeronautics and Space 2 2013-01-01 2013-01-01 false General. 95.11 Section 95.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) AIR TRAFFIC AND GENERAL OPERATING RULES IFR ALTITUDES Designated Mountainous Areas § 95.11 General. The areas described...

  7. 45 CFR 1801.11 - Annual nomination.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 45 Public Welfare 4 2013-10-01 2013-10-01 false Annual nomination. 1801.11 Section 1801.11 Public Welfare Regulations Relating to Public Welfare (Continued) HARRY S. TRUMAN SCHOLARSHIP FOUNDATION HARRY S. TRUMAN SCHOLARSHIP PROGRAM Nominations § 1801.11 Annual nomination. (a) Except as provided in §§...

  8. 45 CFR 1801.11 - Annual nomination.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 45 Public Welfare 4 2012-10-01 2012-10-01 false Annual nomination. 1801.11 Section 1801.11 Public Welfare Regulations Relating to Public Welfare (Continued) HARRY S. TRUMAN SCHOLARSHIP FOUNDATION HARRY S. TRUMAN SCHOLARSHIP PROGRAM Nominations § 1801.11 Annual nomination. (a) Except as provided in §§...

  9. 45 CFR 1801.11 - Annual nomination.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 45 Public Welfare 4 2010-10-01 2010-10-01 false Annual nomination. 1801.11 Section 1801.11 Public Welfare Regulations Relating to Public Welfare (Continued) HARRY S. TRUMAN SCHOLARSHIP FOUNDATION HARRY S. TRUMAN SCHOLARSHIP PROGRAM Nominations § 1801.11 Annual nomination. (a) Except as provided in §§...

  10. 45 CFR 1801.11 - Annual nomination.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 45 Public Welfare 4 2011-10-01 2011-10-01 false Annual nomination. 1801.11 Section 1801.11 Public Welfare Regulations Relating to Public Welfare (Continued) HARRY S. TRUMAN SCHOLARSHIP FOUNDATION HARRY S. TRUMAN SCHOLARSHIP PROGRAM Nominations § 1801.11 Annual nomination. (a) Except as provided in §§...

  11. 45 CFR 1801.11 - Annual nomination.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 45 Public Welfare 4 2014-10-01 2014-10-01 false Annual nomination. 1801.11 Section 1801.11 Public Welfare Regulations Relating to Public Welfare (Continued) HARRY S. TRUMAN SCHOLARSHIP FOUNDATION HARRY S. TRUMAN SCHOLARSHIP PROGRAM Nominations § 1801.11 Annual nomination. (a) Except as provided in §§...

  12. 16 CFR 1507.11 - Party poppers.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... 16 Commercial Practices 2 2012-01-01 2012-01-01 false Party poppers. 1507.11 Section 1507.11 Commercial Practices CONSUMER PRODUCT SAFETY COMMISSION FEDERAL HAZARDOUS SUBSTANCES ACT REGULATIONS FIREWORKS DEVICES § 1507.11 Party poppers. Party poppers (also known by other names such as “Champagne...

  13. 16 CFR 1507.11 - Party poppers.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... 16 Commercial Practices 2 2013-01-01 2013-01-01 false Party poppers. 1507.11 Section 1507.11 Commercial Practices CONSUMER PRODUCT SAFETY COMMISSION FEDERAL HAZARDOUS SUBSTANCES ACT REGULATIONS FIREWORKS DEVICES § 1507.11 Party poppers. Party poppers (also known by other names such as “Champagne...

  14. 16 CFR 1507.11 - Party poppers.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... 16 Commercial Practices 2 2014-01-01 2014-01-01 false Party poppers. 1507.11 Section 1507.11 Commercial Practices CONSUMER PRODUCT SAFETY COMMISSION FEDERAL HAZARDOUS SUBSTANCES ACT REGULATIONS FIREWORKS DEVICES § 1507.11 Party poppers. Party poppers (also known by other names such as “Champagne...

  15. 14 CFR 147.11 - Ratings.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 14 Aeronautics and Space 3 2010-01-01 2010-01-01 false Ratings. 147.11 Section 147.11 Aeronautics and Space FEDERAL AVIATION ADMINISTRATION, DEPARTMENT OF TRANSPORTATION (CONTINUED) SCHOOLS AND OTHER CERTIFICATED AGENCIES AVIATION MAINTENANCE TECHNICIAN SCHOOLS Certification Requirements § 147.11 Ratings....

  16. 46 CFR 11.480 - Radar observer.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 1 2014-10-01 2014-10-01 false Radar observer. 11.480 Section 11.480 Shipping COAST... ENDORSEMENTS Professional Requirements for National Deck Officer Endorsements § 11.480 Radar observer. (a) This section contains the requirements that an applicant must meet to qualify as a radar observer. (b) If...

  17. 46 CFR 11.480 - Radar observer.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 1 2011-10-01 2011-10-01 false Radar observer. 11.480 Section 11.480 Shipping COAST... ENDORSEMENTS Professional Requirements for Deck Officers § 11.480 Radar observer. (a) This section contains the requirements that an applicant must meet to qualify as a radar observer. (Part 15 of this chapter specifies...

  18. 46 CFR 11.480 - Radar observer.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 46 Shipping 1 2012-10-01 2012-10-01 false Radar observer. 11.480 Section 11.480 Shipping COAST... ENDORSEMENTS Professional Requirements for Deck Officers § 11.480 Radar observer. (a) This section contains the requirements that an applicant must meet to qualify as a radar observer. (Part 15 of this chapter specifies...

  19. 46 CFR 11.480 - Radar observer.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 1 2013-10-01 2013-10-01 false Radar observer. 11.480 Section 11.480 Shipping COAST... ENDORSEMENTS Professional Requirements for Deck Officers § 11.480 Radar observer. (a) This section contains the requirements that an applicant must meet to qualify as a radar observer. (Part 15 of this chapter specifies...

  20. 46 CFR 11.480 - Radar observer.

    Code of Federal Regulations, 2010 CFR

    2010-10-01

    ... 46 Shipping 1 2010-10-01 2010-10-01 false Radar observer. 11.480 Section 11.480 Shipping COAST... ENDORSEMENTS Professional Requirements for Deck Officers § 11.480 Radar observer. (a) This section contains the requirements that an applicant must meet to qualify as a radar observer. (Part 15 of this chapter specifies...