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A pancake-type transmission chamber made of high-purity graphite and open to the atmosphere has been designed and constructed at the Secondary Standard Dosimetry Laboratory (SSDL-Rio de Janeiro). Tests performed on the chamber following the International Electrotechnical Commission recommendations indicate that its performance characteristics are comparable to those expected from a secondary standard ionization chamber.
High-resolution transmission electron microscopy, shows that carbon in the Allende carbonaceous chondrite meteorite is predominantly a poorly crystalline graphite. Such material is of interest as an important carrier of the isotopically anomalous noble gases found in carbonaceous chondrites.
Highly ordered pyrolytic graphite (HOPG) is the substrate often used in scanning tunneling microscope (STM) studies of biomolecules such as DNA. All of the images presented in this article are of freshly cleaved HOPG surfaces upon which no deposition has occurred. These images illustrate features previously thought to be due to biological molecules, such as periodicity and meandering of "molecules" over steps. These features can no longer be used to distinguish real molecules from features of the native substrate. The feasibility of the continued use of HOPG as a substrate for biological STM studies is discussed.
Matrix olivines in the Allende carbonaceous chondrite are believed to have formed by condensation processes in the primitive solar nebula. However, transmission electron microscope observations of numerous matrix olivines show that they contain abundant, previously unrecognized, nanometer-sized inclusions of pentlandite and poorly graphitized carbon. Neither of these phases would have been stable at the high-temperature conditions required to condense iron-rich olivine in the solar nebula. The presence of these inclusions is consistent with formation of the olivines by parent body processes that involved overgrowth of fine-grained organic materials and sulfides in the precursor matrix materials.
The transfer of electrons from one material to another is usually described in terms of energy conservation, with no attention being paid to momentum conservation. Here we present results on the junction resistance between a carbon nanotube and a graphite substrate and show that details of momentum conservation also can change the contact resistance. By changing the angular alignment of the atomic lattices, we found that contact resistance varied by more than an order of magnitude in a controlled and reproducible fashion, indicating that momentum conservation, in addition to energy conservation, can dictate the junction resistance in graphene systems such as carbon nanotube junctions and devices.
Desulfobulbus propionicus was able to grow with Fe(III), the humic acids analog anthraquinone-2,6-disulfonate (AQDS), or a graphite electrode as an electron acceptor. These results provide an explanation for the enrichment of Desulfobulbaceae species on the surface of electrodes harvesting electricity from anaerobic marine sediments and further expand the diversity of microorganisms known to have the ability to use both sulfate and Fe(III) as an electron acceptor.
BACKGROUND AND AIMS: To examine the risk for cancer mortality among workers exposed to coal tar and coal tar pitch volatiles in a man-made graphite electrode factory. The risk for cancer mortality in this type of factory is still inconclusive, although coal tar and coal tar pitch are recognised as human carcinogens. METHODS: The study cohort consisted of 332 male employees who served more than five years in the period 1951-74. The cohort was traced until 1988. Analyses used standardised mortality ratios (SMRs) to compare cause specific mortality with that in the general and local population. Effect of smoking was estimated based on the information collected from the subgroup of the cohort. SMRs for leading causes of death were compared among different job titles, duration of employment, time since first employment, and observation subperiods. Exposure level for tar and benzo[a]pyrene (BaP) in the factory was also discussed, based on measurements done by other researchers in the past. RESULTS: During the study period, 52 deaths were identified (SMR 0.68), including 22 cancer deaths (SMR 1.01). The SMR for lung cancer was significantly increased in comparison with the general population (SMR 2.62). It was slightly decreased in comparison with the local population, but remained significant (SMR 2.35). Excess deaths were also observed for lymphatic and haematopoietic cancers (SMR 3.46). Smoking habits in the subgroup were similar to those in the general population; thus the increased SMR for lung cancer was unlikely to be explained by smoking. CONCLUSION: Previous environmental measurements suggested that considerable exposure to tar and BaP had existed in the factory. The results suggest a possible risk for lung cancer among the cohort, but the limitations of the study, such as the small study population and insufficient information on exposure, indicate that further study is required.
Graphitic carbon nanofibers (GCNFs) are prepared from CO/H2 with a nickel-rich Fe-Ni (2:8) growth catalyst supported on three different water-soluble supports (Na4SiO4, Na2SiO3, and Na2CO3). GCNF products are formed with yield and crystallinity comparable to those of GCNF product produced with the same growth catalyst supported on fumed silica. Separation of GCNF product from the solid support is accomplished by aqueous dissolution of the support. This synthetic method extends the convenient isolation of GCNFs formed with supported growth catalysts to a wide variety of potential solid supports.
Processing methods have been optimized for the formation of graphitic carbon nanofiber (GCNF)/epoxy nanocomposites containing GCNFs highly dispersed throughout a thermoset epoxy matrix. GCNFs having a herringbone atomic structure are surface-derivatized with bifunctional hexanediamine linker molecules (GCNF-HDA) capable of covalent binding to an epoxy matrix during thermal curing and are cut to smaller dimension using high-power ultrasonication. GCNF-HDA nanofibers are dispersed in epoxy resin at 0.3 wt.% loading using variable levels of ultrasonication processing prior to thermal curing. Effects of sonication power on the quality of the GCNF-HDA/epoxy material obtained after curing have been determined from flexural property measurements, thermomechanical analysis and SEM/TEM imaging. GCNF-HDA/epoxy material of the highest quality is obtained using low-power sonication, although high-power sonication for short periods gives improved flexural properties without lowering the glass transition temperature. Good dispersion and polymer wetting of the GCNF component is evident on the nanoscale.
Carbon nanofiber/silica aerogel composites are prepared by sol-gel processing of surface-enhanced herringbone graphitic carbon nanofibers (GCNF) and Si(OMe)4, followed by supercritical CO2 drying. Heating the resulting GCNF/silica aerogel composites to 1650 degrees C under a partial pressure of Ar gas initiates carbothermal reaction between the silica aerogel matrix and the carbon nanofiber component to form SiC/silica nanocomposites. The SiC phase is present as nearly spherical nanoparticles, having an average diameter of ca. 8 nm. Formation of SiC is confirmed by powder XRD and by Raman spectroscopy.
We have completed a preliminary series of experiments that compare the silicate shells of the marine organism diatoms to Single-Wall NanoTubes (SWNT), Multi-Wall NanoTubes (MWNT), Exfoliated Graphite (EG), and silica as templates for producing nanostructures of the manganese acetate cluster Mn12 (Mn12[CH3(COO)16(H2O)4O12].(2)CH3COOH.4H2O). Mn12 exhibits magnetic properties because of the molecular arrangement within the cluster and exhibits no exchange couplings between the individual clusters. Data from scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), and laser diffraction are discussed in terms of research that can expand the use of diatoms and other materials as templates for nanostructures.
The chromatographic behavior of manno-oligosaccharides derived from Saccharomyces cerevisiae mannan on two kinds of HPLC columns, an aminopropyl-silica column or a graphitized carbon column (GCC), was investigated. The order of elution of manno-oligosaccharides on both columns with acetonitrile-water was almost the same, that is, the retention increased with increasing molecular size. However, the GCC made it possible to isolate completely two isomers of mannotrioses (M(3)-1 and M(3)-2) with different linkage positions. We reinvestigated the structures of mannobiose (M(2)), M(3)s, and mannotetraose (M(4)) that were completely isolated by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) and NMR spectroscopy.
Xanthine oxidase (E. C. 1.2.3.2) was immobilized by adsorption on electrochemically modified graphite plate to obtain an enzyme electrode. The current of the enzyme electrode in substrate (xanthine) solutions was found to be a result of the electrooxidation of H2O2 generated in the enzyme layer. The linearity of the amperometric signal was up to a substrate concentration of 65 microM at 0.6 V (vs. Ag/AgCl). The response time was 2 minutes. The enzyme electrode preserves 80% of its initial activity after a three-week storage in air at room temperature.
Glucose oxidase (E. C. 1.1.3.4) was immobilized on electrochemically modified graphite to obtain an enzyme electrode. The working surface of the electrode was coated with gelatine to prevent desorption of the enzyme. In substrate (glucose) solutions the amperometric signal of the enzyme electrode was due to the electroreduction of H202 generated in the enzyme layer. The linearity of the electrode response was found up to a substrate concentration of 300 microM at a working potential of 0 mV (vs. Ag/AgCl). It was shown that the electrode did not respond to L-ascorbic and uric acid at that working potential. The response time was about 2 min. The enzyme electrode keeps about 50% of its initial activity after a one-week storage at 4 degrees C.
Scalp hair samples were decomposed by the semimicro wet digestion method and transferred into test tubes (15 ml) equipped with face abraded exchangeable stoppers. To the test solution (5 ml), citric buffer was added and the pH was adjusted to 3.0, and water was added to make the solution 10 ml. Iron and other few ions are extracted with 1% oxine-MIBK solution (1 ml) and removed. Then, lead was extracted with APDC-MIBK solution (1 ml), and the upper layer (20 microliters) was injected immediately into graphite-tube. Atomic absorption was measured at 2,170 A corrected background by D2 lamp. Recovery tests of lead added to hair samples were satisfactory and interference by coexisting metals was not observed. With this method, the amount of lead in hair samples from healthy persons were determined, and the mean values of 4.90 ppm in male and 8.13 ppm in female were indicated.
The chlorosomal light-harvesting antennae of green phototrophic bacteria consist of large supramolecular aggregates of bacteriochlorophyll c (BChl c). The supramolecular structure of (3(1)-R/S)-BChl c on highly oriented pyrolytic graphite (HOPG) and molybdenum disulfide (MoS2) has been investigated by scanning tunneling microscopy (STM). On MoS2, we observed single BChl c molecules, dimers or tetramers, depending on the polarity of the solvent. On HOPG, we observed extensive self-assembly of the dimers and tetramers. We propose C=O...H-O...Mg bonding networks for the observed dimer chains, in agreement with former ultraviolet-visible and infrared spectroscopic work. The BChl c moieties in the tetramers are probably linked by four C=O...H-O hydrogen bonds to form a circle and further stabilized by Mg...O-H bondings to underlying BChl c layers. The tetramers form highly ordered, distinct chains and extended two-dimensional networks. We investigated semisynthetic chlorins for comparison by STM but observed that only BChl c self-assembles to well-structured large aggregates on HOPG. The results on the synthetic chlorins support our structure proposition.
A spectral mapping technique (SPM) was employed for separating the strength and selectivity of the retention of 41 barbituric acid derivatives and 5 organic modifiers on a porous graphitized carbon column (PGC). The potency values calculated by SPM were considered to be indicators of the capacity of drugs to bind to the surface of PGC and the capacity of organic modifiers to remove the drugs from the surface. The dimensionality of the multidimensional selectivity maps was reduced to two by a nonlinear mapping technique. Calculations indicated that molecular lipophilicity plays a negligible role in the strength and selectivity of retention, proving that the retention mechanism of PGC deviates from those of traditional reversed-phase stationary phases. Sterical and electronic parameters exerted the highest influence on the retention, emphasizing the importance of the polar interaction and the sterical correspondence between the surface of PGC and the solute molecules.
A method has been described for the determination of total mercury by graphite-furnace atomic absorption spectrometry (GFAAS) using an in-situ concentration technique with a Pd-Zr coating and a chemical modifier. The characteristic mass, which gives an integrated absorbance of 0.0044 s, was found to be 42 pg and an absolute detection limit (3sigma) of 33 pg was obtained with the proposed modifier. The total mercury values in standard reference materials, including Mussel (GBW08571), Bovine liver (GBW08306), Peach leaf (GBW08501) and Tea leaf (GBW080001), were determined using the proposed method, and the results were consistent with reference values. The method had been successfully applied to the determination of mercury in biological tissue samples with a recovery range of 94-105%.