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At least 127 records · Page 7Linked to original sources
PubMed1995

Porous graphitic carbon shows promise for the rapid chromatographic analysis of polar drug metabolites.

A rapid and simple HPLC method has been developed and used to separate the polar metabolic conjugates of AZT, chloramphenicol, and beta-estradiol based upon the use of porous graphitic carbon. The HPLC system is sufficiently selective to resolve the polar drug conjugates from their parent compounds and from endogenous material present in urine. The compounds are separated, without the need for sample pretreatment or gradient elution, on a porous graphitic carbon (Hypercarb) column using aqueous trifluoroacetic acid modified with tetrahydrofuran as the mobile phase. Porous graphitic carbon exhibits a novel mechanism of retention towards these very polar substances, which are unretained under reversed-phase conditions on alkyl-bonded silica phases.

Animals↗
PubMed2005

Oxidative coupling and the irreversible adsorption of phenol by graphite.

Uptake of phenol by graphite, and regeneration by methanol extraction, was measured to evaluate irreversible adsorption of phenols to carbon surfaces. The emphasis of this work was to identify the role of oxidative coupling, which has been invoked to explain irreversible phenol sorption by activated carbons. Graphite was chosen as a model carbon surface to eliminate potentially confounding effects of microporosity present in other types of carbonaceous sorbents. The isotherm data were well described by the Langmuir-Freundlich isotherm from pH 3 to 9. At pH 12, measured uptakes were higher than expected based on model predictions, suggesting the occurrence of an adsorption mechanism besides physisorption. One oxidative coupling product, 2,2'-dihydroxybiphenyl, was obtained exclusively after adsorption at pH values above 7, and appeared both in aqueous solution and in the methanol regenerant solution. The fraction of total uptake that was not recoverable by methanol extraction decreased with increasing phenol concentration in solution, suggesting preferential sorption by high-energy sites. However, absolute irreversible adsorption increased with phenol concentration in solution. Both fractional irreversible adsorption and 2,2'-dihydroxybiphenyl oxidative coupling product recovery as a function of pH and contact time demonstrated that irreversible sorption of phenol by graphite could not be explained by an oxidative coupling mechanism alone.

Adsorption↗
PubMed2006

Removal of disperse blue 2BLN from aqueous solution by combination of ultrasound and exfoliated graphite.

This paper reports an efficient and convenient removal of disperse blue 2BLN from aqueous solution by the combination of ultrasound and exfoliated graphite. The various affecting factors were studied. The removal ratio of disperse blue 2BLN is 96.9% for the initial concentration of 200 mg/L using 600 mg/L exfoliated graphite (exfoliation volume of 300 mL/g) at 45 degrees C within 120 min under ultrasound. The combination method was more effective than sonolysis or exfoliated graphite treatment individually.

Absorption↗
PubMed2006

Decolorization of azo dye direct scarlet 4BS solution using exfoliated graphite under ultrasonic irradiation.

A combination of ultrasound and exfoliated graphite has been used to treat wastewater containing direct scarlet 4BS for colour removal and for the reduction of absorption at a wavelength of 242 nm. The results show that the ultrasound/exfoliated graphite process is effective in removing direct scarlet 4BS from aqueous solution. Furthermore, it can achieve better results than either exfoliated graphite or ultrasound alone.

Azo Compounds↗
PubMed2001

TL response study of the CaSO4:Dy pellets with graphite for dosimetry in beta radiation and low-energy photons fields.

The CaSO4:Dy is a good thermoluminescent dosimeter because of its high sensitivity and low cost. With graphite in the pellets it is possible to reduce the energy dependence. The sensitivity and energy dependence of the different thicknesses of CaSO4:Dy pellets was studied with different amounts of graphite. The results have shown the optimal quantity of the graphite and the appropriate thickness of the pellets that can be used in dosimetry of beta field, photons or both simultaneously.

Beta Particles↗
PubMed2004

Sub-parts-per-quadrillion-level graphite furnace atomic absorption spectrophotometry based on laser wave mixing.

Nonlinear laser wave mixing in a common graphite furnace atomizer is presented as a zeptomole-level, sub-Doppler, high-resolution atomic absorption spectrophotometric method. A nonplanar three-dimensional wave-mixing optical setup is used to generate the signal beam in its own space. Signal collection is efficient and convenient using a template-based optical alignment. The graphite furnace atomizer offers advantages including fast and convenient introduction of solid, liquid, or gas analytes, clean atomization environment, and minimum background noise. Taking advantage of the unique features of the wave-mixing optical method and those of the graphite furnace atomizer, one can obtain both excellent spectral resolution and detection sensitivity. A preliminary concentration detection limit of 0.07 parts-per-quadrillion and a preliminary mass detection limit of 0.7 ag or 8 zmol are determined for rubidium using a compact laser diode as the excitation source.

Graphite↗
PubMed2005

Diazonium-protein adducts for graphite electrode microarrays modification: direct and addressed electrochemical immobilization.

Diazonium cation electrodeposition was investigated for the direct and electro-addressed immobilization of proteins. For the first time, this reaction was triggered directly onto diazonium-modified proteins. Screen-printed (SP) graphite electrode microarrays were studied as active support for this immobilization. A 10-microelectrode (eight working electrodes, 0.2 mm2 each; one reference; and one auxiliary) setup was used to study the addressing possibilities of the method. These electrode microarrays were shown to be able to covalently graft diazonium cations through electrochemical reduction. Cyclic voltammetry and X-ray photoelectron spectroscopy were used to characterize the electrochemical grafting onto our SP graphite surface and suggested that a diazonium monolayer was deposited. Rabbit and human immunoglobulins (IgGs) were then chemically coupled to an aniline derivative (4-carboxymethylaniline), followed by diazotation to form an aryl diazonium function available for the electrodeposition. These modified proteins were both successfully electro-addressed at the surface of the graphite electrodes without cross-talk or interference. The immuno-biochip obtained using this novel approach enabled the specific detection of anti-rabbit IgG antibodies with a detection limit of 50 fmol of protein. A promising strategy to immobilize markedly different biological entities was then presented, providing an excellent spatial specificity of the electro-addressing.

Animals↗
PubMed2005

Chirality in supramolecular self-assembled monolayers of achiral molecules on graphite: formation of enantiomorphous domains from arachidic anhydride.

The molecular arrangement and chirality of the self-assembled arachidic anhydride monolayer on graphite were investigated using scanning tunneling microscopy (STM). This molecule has two identical alkyl chains, linked by an anhydride group in the middle. In its extended form, one alkyl chain is shifted, with respect to the other, along the molecular backbone. Upon adsorption on graphite, this achiral anhydride spontaneously forms two types of homogeneous domains (denoted as m and m') with mirror symmetry. The angle from the molecular chain to the row-packing direction is 98.0 degrees +/- 0.5 degrees and 82.0 degrees +/- 0.5 degrees for domains m and m', respectively. Domain m is the mirror image of m'. The molecular arrangement of this self-assembled monolayer shows that domains m and m' are two-dimensional enantiomers with opposite chiralities. This new molecular packing motif is confirmed by line-profile analyses along the molecule-chain and the row-packing directions. This finding demonstrates the spontaneous formation of highly ordered homogeneous enantiomorphous domains on graphite resulting only from weak van der Waals forces between the achiral arachidic anhydride molecules.

Adsorption↗
PubMed2005

Coulomb oscillations and Hall effect in quasi-2D graphite quantum dots.

We perform low-temperature electrical transport measurements on gated, quasi-2D graphite quantum dots. In devices with low contact resistances, we use longitudinal and Hall resistances to extract carrier densities of 9.2-13 x 10(12) cm(-2) and mobilities of 200-1900 cm(2)/V.s. In devices with high resistance contacts, we observe Coulomb blockade phenomena and infer the charging energies and capacitive couplings. These experiments demonstrate that electrons in mesoscopic graphite pieces are delocalized over nearly the whole graphite piece down to low temperatures.

Electric Conductivity↗
PubMed2005

Exploration of gas sensing possibilities with edge plane pyrolytic graphite electrodes: nitrogen dioxide detection.

The voltammetric response of nitrogen dioxide in aqueous sulfuric acid using an edge plane pyrolytic graphite electrode has been explored and contrasted with that from basal plane pyrolytic graphite, glassy carbon or boron-doped diamond electrodes. Edge plane graphite electrode is found to produce an excellent voltammetric signal in comparison with other carbon-based electrodes exhibiting a well-defined analytically useful voltammetric redox couple in 2.5 M sulfuric acid which is absent on the alternative electrodes.

Electrochemistry↗
PubMed1999

Analysing organophosphorus pesticides in wines using graphitized carbon black extraction cartridges.

A quick and simple method was developed to determine the residues of 15 organophosphorus pesticides of different polarity in grape wine, based on liquid-solid extraction with graphitized carbon black cartridges and capillary gas chromatography. Aliquots of diluted wine (10 ml wine + 40 ml deionized water) and 250 mg graphitized carbon black cartridges were used to extract the analytes. The pesticides were eluted with 2 x 0.5 ml acetone and 3 x 2.5 ml ethyl acetate/acetone (80:20). The eluates were then dried with anhydrous sodium sulphate and concentrated to 1 ml under a nitrogen current. After adding triphenylphosphate internal standard (i.s.), this extract was analysed by capillary gas chromatography using a nitrogen-phosphorus detector (GC-NPD). Pesticide recovery percentages at levels of 0.01 and 0.02 microgram/ml were between 74% and 111%, with a 2-13% relative standard deviation interval. The chromatograms of extracts had few co-extracted species peaks, with no analytical interference. Dilution of the grape wine samples removed most of the pigments, thus producing clear extracts. The results indicate that liquid-solid extraction from wine samples using graphitized carbon is fast (25 min per sample), efficient and reproducible for analysing organophosphorus pesticides of different polarity.

Chromatography, Gas↗
PubMed1977

Graphite-mixed CaSo4: Dy teflon TLD discs for beta dosimetry.

The thickness of commonly employed thermoluminescent dosemeters (TLDS) is responsible for the problem of energy dependence in beta dose estimation in situations where this thickness is comparable to the range of beta particles in the TLD material. The effective thickness of solid TLD discs can, however, be reduced by use of some additives which would reduce their transparency to the TL light. The incorporation of various amounts of graphite powder into 0-8 mm thick CaSO4: Dy Teflon TLD discs has been investigated. This has considerably reduced their energy dependence for beta rays with Emax values ranging from 0-4 MeV to 2-27 MeV. Addition of graphite also results in sharp glow curves thereby minimizing the heating time during TL measurements. Significantly, graphite was also found to reduce the non-radiation-induced TL signal and this helps in low dose measurements.

Calcium↗
PubMed1990

The thermal defect of A-150 plastic and graphite for low-energy protons.

The thermal defects of A-150 plastic and graphite referenced to aluminium were determined for 800 keV protons scattered by a 2 micron nickel foil (mean transmitted energy = 550 keV). Composite cores of Al/A-150, graphite/A-150 and Al/graphite which could be irradiated from one side or the other were employed. The temperature increase of a core caused by 30-100 s of irradiation (3-6 nA of proton beam current) was detected by two thermistors mounted in opposite legs of a Wheatstone bridge. The thermal defect of A-150 plastic was determined to be 0.0421 +/- 0.0036 (SE) referenced to aluminium and 0.0402 +/- 0.0034 referenced to graphite. The thermal defect of graphite referenced to aluminium is 0.0043 +/- 0.0034. No change in the thermal defect of A-150 plastic was detected for accumulated doses up to 8 x 10(5) Gy.

Aluminum↗
PubMed2002

Evaluation of factors to convert absorbed dose calibrations from graphite to water for the NPL high-energy photon calibration service.

The National Physical Laboratory (NPL) provides a high-energy photon calibration service using 4-19 MV x-rays and 60Co gamma-radiation for secondary standard dosemeters in terms of absorbed dose to water. The primary standard used for this service is a graphite calorimeter and so absorbed dose calibrations must be converted from graphite to water. The conversion factors currently in use were determined prior to the launch of this service in 1988. Since then, it has been found that the differences in inherent filtration between the NPL LINAC and typical clinical machines are large enough to affect absorbed dose calibrations and, since 1992, calibrations have been performed in heavily filtered qualities. The conversion factors for heavily filtered qualities were determined by interpolation and extrapolation of lightly filtered results as a function of tissue phantom ratio 20,10 (TPR20,10). This paper aims to evaluate these factors for all mega-voltage photon energies provided by the NPL LINAC for both lightly and heavily filtered qualities and for 60Co y-radiation in two ways. The first method involves the use of the photon fluence-scaling theorem. This states that if two blocks of different material are irradiated by the same photon beam, and if all dimensions are scaled in the inverse ratio of the electron densities of the two media, then, assuming that all photon interactions occur by Compton scatter the photon attenuation and scatter factors at corresponding scaled points of measurement in the phantom will be identical. The second method involves making in-phantom measurements of chamber response at a constant target-chamber distance. Monte Carlo techniques are then used to determine the corresponding dose to the medium in order to determine the chamber calibration factor directly. Values of the ratio of absorbed dose calibration factors in water and in graphite determined in these two ways agree with each other to within 0.2% (1sigma uncertainty). The best fit to both sets of results agrees with values determined in previous work to within 0.3% (1sigma uncertainty). It is found that the conversion factor is not sensitive to beam filtration.

Calibration↗
PubMed2004

A small-body portable graphite calorimeter for dosimetry in low-energy clinical proton beams.

Calorimetry has been recommended and performed in proton beams for some time, but never has graphite calorimetry been used as a reference dosimeter in clinical proton beams. Furthermore, only a few calorimetry measurements have been reported in ocular proton beams. In this paper we describe the construction and performance of a small-body portable graphite calorimeter for clinical low-energy proton beams. Perturbation correction factors for the gap effect, volume averaging effect, heat transfer phenomena and impurity effect are calculated and applied in a comparison with ionization chamber dosimetry following IAEA TRS-398. The ratio of absorbed dose to water obtained from the calorimeter measurements and from the ionization measurements varied between 0.983 and 1.019, depending on the beam type and the ionization chamber calibration modality. Standard uncertainties on these values varied between 1.9% and 2.5% including a substantial contribution from the kQ values in IAEA TRS-398. The (Wair/e)p values inferred from these measurements varied between 33.6 J C(-1) and 34.9 J C(-1) with similar standard uncertainties. A number of improvements for the small-body portable graphite calorimeter and the experimental set-up are suggested for potential reduction of the uncertainties.

Calibration↗
PubMed1997

A cohort study of graphite workers in Sri Lanka.

A cohort of workers from a graphite mine in Sri Lanka was studied in 1987, 1990 and 1993. Radiographic lesions were found in 8.5%, 8.9% and 4.1% of the workers in these respective rounds. When workers with radiographic lesions were clinically examined, a total of 18 cases of graphite pneumoconiosis and seven cases of active pulmonary tuberculosis were detected in the three rounds. The prevalence of both these diseases showed a decline in 1993 when compared to 1987. This favourable situation was probably the result of dust control measures introduced in the mine after 1972. Five workers developed graphite pneumoconiosis in the course of the study. They had worked in the mine for an average of 22.6 years. The right lung appeared to be more vulnerable than the left.

Adult↗
PubMed2004

Raman spectroscopy of graphite.

We present a review of the Raman spectra of graphite from an experimental and theoretical point of view. The disorder-induced Raman bands in this material have been a puzzling Raman problem for almost 30 years. Double-resonant Raman scattering explains their origin as well as the excitation-energy dependence, the overtone spectrum and the difference between Stokes and anti-Stokes scattering. We develop the symmetry-imposed selection rules for double-resonant Raman scattering in graphite and point out misassignments in previously published works. An excellent agreement is found between the graphite phonon dispersion from double-resonant Raman scattering and other experimental methods.

Biophysics↗
PubMedDate not supplied

Comparisons of calorimetric and ionometric measurements in graphite irradiated with electrons from 15 to 50 MeV.

Extensive experimental comparisons of calorimetric and ionometric measurements have been made that cover a broader range of electron energies and depths in graphite than previously reported. Electron beams of 15, 20, 25, 30, 40, and 50 MeV were used. Calorimetric absorbed-dose measurements and ionometric specific-charge measurements in air were compared in graphite at depths from 1 to 51 g/cm2. The medium was irradiated with uncollimated electron beams produced by scattering after passing through a 0.1-g/cm2 aluminum vacuum window, various thicknesses of lead foils, and air. The variation in the quotient of the two measurements was studied as a function of lead-foil thickness, depth in the medium, beam energy, foil-to-detector distance, and off-axis distance. These studies permitted the measurements to be corrected and compared with theoretical calculations that assume a broad medium irradiated with broad, parallel, monoenergetic electron beams. The overall experimental uncertainty is estimated to be 1%. The results are generally in good agreement with theoretical and experimental results of other investigators. The calorimeter received close to 1 Mrad during preliminary measurements and from 1 to 2 Mrad during the measurements reported. The results showed no detectable heat defect in graphite after prolonged periods of exposing the calorimeter to air at atmospheric pressure.

Calorimetry↗