Prompt-gamma neutron activation analysis system design: Effects of D-T versus D-D neutron generator source selection

Prompt-gamma neutron activation (PGNA) analysis is used for the non-invasive measurement of human body composition. Advancements in portable, compact neutron generator design have made those devices attractive as neutron sources. Two distinct generators are available: D-D with 2.5 MeV and D-T with 14.2 MeV neutrons. To compare the performance of these two units in our present PGNA system, we performed Monte Carlo simulations (MCNP-5; Los Alamos National Laboratory) evaluating the nitrogen reactions produced in tissue-equivalent phantoms and the effects of background interference on the gamma-detectors. Monte Carlo response curves showed increased gamma production per unit dose when using the D-D generator, suggesting that it is the more suitable choice for smaller sized subjects. The increased penetration by higher energy neutrons produced by the D-T generator supports its utility when examining larger, especially obese, subjects. A clinical PGNA analysis design incorporating both neutron generator options may be the best choice for a system required to measure a wide range of subject phenotypes.     

Estimation of background interference in prompt-gamma neutron activation using MCNP

Prompt-gamma neutron activation (PGNA) is used to measure total-bodynitrogen and hydrogen in humans. Background interference in the gamma spectraarises from both subject and shielding. A Monte Carlo simulation program (MCNP4B2)was used to examine the neutron and gamma signals in the PGNA system ( ²⁴¹AmBe source). N and H peak regions were assessed in the presenceand absence of calibration phantoms. The simulations suggested extracorporealH peak contributions of up to 30%, depending on subject body habitus. MostN background could be attributed to detector pileup events. The MCNP resultsallowed us to improve shielding design and develop background correction algorithmsto improve measurement precision.     

Assessment of the associated particle prompt gamma neutron activation technique for total body nitrogen measurement in vivo

Total body nitrogen (TBN) can be used to estimate total body protein, an important body composition component at the molecular level. A system using the associated particle technique in conjunction with prompt gamma neutron activation analysis has been developed for the measurement of TBN in vivo. The system uses a compact D, T neutron generator (~10⁷ n/s) coupled to an internal alpha-particle detector, and a counting system with six bismuth germinate detectors. 14 Subjects were scanned from shoulders to hips (20 min scan time, <0.4 mSv dose) generating complex spectra dominated by signals from C, O, H, and N, with significant peak overlap. Fractional contributions from these elements to regions of interests (ROI) spanning a 4–8 MeV range were determined by algorithms comparing ratios of interrelated ROIs. In addition, multi-component least squares fitting was done to further resolve individual peak activities (MATLAB R2011b). Total body potassium (TBK) was also measured using a whole body gamma counter. Predicted TBN values, based on fat-free mass estimated from TBK, were compared to measured TBN results. Measured versus predicted results for all subjects were not statistically different. Separating subjects by gender also showed no difference between measured and predicted values. The associated particle system showed good agreement with predicted TBN values, but measurement precision was not better than that commonly seen in traditional prompt gamma thermal neutron activation analysis systems.     

Experimental Evaluation of a Portable Neutron-Based Gamma-Spectroscopy System for Chloride Measurements in Reinforced Concrete

A portable prompt gamma neutron activation (PGNA) spectroscopy system has been developed to analyze the elemental composition (Ca, Si, Al, etc.) of reinforced concrete and to measure chloride contamination. The portable PGNA system consists of a high purity germanium (HPGe) gamma detector with a 70% relative efficiency, a ²⁵²Cf neutron source and moderator subsystem, and a portable multichannel analyzer system integrated with a laptop computer. Two types of activation experiments were performed to evaluate the device: first, a detector calibration using a Cl gamma standard provided by a PGNA facility; second, an evaluation of the actual performance of the complete system with the ²⁵²Cf source using full scale test slabs containing known amounts of chloride. Both methods indicate that it is feasible to use this device to measure the chloride content of reinforced concrete in the field. The chloride level for the corrosion threshold can be measured with a precision of 10% for a counting time of roughly 6 minutes. This makes the PGNA method competitive with the conventional destructive method.     

Total body sodium and chlorine in normal adults as determined by neutron activation analysis

Total body neutron activation analysis (TBNAA) has used to determine the absolute levels of total body sodium (TBNa) and total body chlorine (TBCl) in 81 normal adults. For the age span studied (30–90 years), the mean values of TBNa and TBCl remained relatively constant for males, but decreased slightly for females beyond sixty years of age. In order to reduce the variability in this cross-sectional study, the TBNa and TBCl values were normalized for body dimensions (weight, height, body surface area) as well as age and sex. In addition, TBNa was related to skeletal mass (total body calcium) and lean body mass (total body potassium). The quantity of body sodium in excess of the chlorine space was determined. This value, defined as sodium excess, was significantly correlated with total body calcium. The values for total body sodium, total body chlorine, and sodium excess obtained in the present study were compared with values previously reported in the literature.     

Evaluation of New Pharmaceuticals Using In Vivo Neutron Inelastic Scattering and Neutron Activation Analysis

Nutritional status of patients can be evaluated by monitoring changes in body composition, including depletion of protein and muscle, adipose tissue distribution and changes in hydration status, bone or cell mass. Fast neutron activation (for N and P) and neutron inelastic scattering (for C and O) are used to assess in vivo elements characteristic of specific body compartments. The fast neutrons are produced with a sealed deuterium-tritium (D-T) neutron generator. This method provides the most direct assessment of body composition. Non-bone phosphorus for muscle is measured by the ³¹P(n,)²⁸Al reaction, and nitrogen for protein via the (n,2n) fast neutron reaction. Inelastic neutron scattering is used for the measurement of total body carbon and oxygen. Carbon is used to derive body fat, after subtracting carbon contributions due to protein, bone and glycogen. Carbon-to-oxygen (C/O) ratio is used to measure distribution of fat and lean tissue in the body and to monitor small changes of lean mass and its quality. In addition to evaluating the efficacy of new treatments, the system is used to study the mechanisms of lean tissue depletion with aging and to investigate methods for preserving function and quality of life in the elderly.     

Large sample neutron activation analysis of a reference inhomogeneous sample

A benchmark experiment was performed for Neutron Activation Analysis (NAA) of a large inhomogeneous sample. The reference sample was developed in-house and consisted of SiO₂ matrix and an Al–Zn alloy “inhomogeneity” body. Monte Carlo simulations were employed to derive appropriate correction factors for neutron self-shielding during irradiation as well as self-attenuation of gamma rays and sample geometry during counting. The large sample neutron activation analysis (LSNAA) results were compared against reference values and the trueness of the technique was evaluated. An agreement within ±10% was observed between LSNAA and reference elemental mass values, for all matrix and inhomogeneity elements except Samarium, provided that the inhomogeneity body was fully simulated. However, in cases that the inhomogeneity was treated as not known, the results showed a reasonable agreement for most matrix elements, while large discrepancies were observed for the inhomogeneity elements. This study provided a quantification of the uncertainties associated with inhomogeneity in large sample analysis and contributed to the identification of the needs for future development of LSNAA facilities for analysis of inhomogeneous samples.     

Extension of the measuring range of balances

The basic principle of comparing the sample mass with the mass of a reference body in equilibrium gives the equal-armed beam balance a unique accuracy. Main parameters characterising the suitability of the instrument are measuring range, resolution and relative sensitivity (resolution/maximum load). The historical development of the values of these parameters achieved depended strongly on the practical need in those times. Technically unfavourable scales of the oldest Egyptian dynasties (~3000 BC) could resolve mass differences of 1 g and had a relative sensitivity of at least 10^–3. More sophisticated instruments from the 18^th Dynasty (~1567–1320 BC) achieved a relative sensitivity of 10^–4 independent of the size of the instrument. In 350 BC Aristotle clarified the theory of the lever and at about 250 BC Archimedes used the balance for density determinations of solids. The masterpiece of a hydrological balance was Al Chazini’s 'Balance of Wisdom’ built about 1120. Its relative sensitivity was 2⋅10^–5. Real progress took place when scientists like Lavoisier (1743–1794) founded modern chemistry. At the end of the 19^th century metrological balances reached a relative sensitivity of 10^–9 with a maximum load of several kilogrammes. That seems to be the high end of sensitivity of the classical mechanical beam balance with knife edges. Improvements took place by electrodynamic compensation (Emich, Gast). In 1909 Ehrenhaft and Millikan could weigh particles of 10^–15 g by means of electrostatic suspension. In 1957 Sauerbrey invented the oscillating quartz crystal balance. By observing the frequency shift of oscillating carbon nanotubes or of silica nanorods, masses or mass changes in the attogram or zeptogram have been observed recently.     

The determination of uranium in biological materials by neutron activation analysis using the fission product134I

A method for the determination of uranium based on²³⁵U thermal neutron fission, has been developed and employed on samples of ashed fish tissue and seaweed. The method involves a post-irradiation ion exchange separation of iodine isotopes. The 884 keV photopeak of¹³⁴I is used for measurement. Uranium detection limits in the samples concerned have been estimated to be 1·10⁻⁸g in terms of natural uranium. The precision achieved in analysing several series of 3–5 samples was 4–10 per cent. The accuracy of the method was tested by employing an independent neutron activation procedure based on²³⁹U measurement. The accuracy of both methods was checked by analysing NBS SRM 1571 ‘Orchard Leaves’.     

Use of D–T-produced fast neutrons for in vivo body composition analysis: a reference method for nutritional assessment in the elderly

Body composition has become the main outcome of many nutritional intervention studies including osteoporosis, malnutrition, obesity, AIDS, and aging. Traditional indirect body composition methods developed with healthy young adults do not apply to the elderly or diseased. Fast neutron activation (for N and P) and neutron inelastic scattering (for C and O) are used to assess in vivo elements characteristic of specific body compartments. Non-bone phosphorus for muscle is measured by the ³¹P(n,)²⁸Al reaction, and nitrogen for protein via the ¹⁴N(n,2n)¹³N fast neutron reaction. Inelastic neutron scattering is used to measure total body carbon and oxygen. Body fat is derived from carbon after correcting for contributions from protein, bone, and glycogen. Carbon-to-oxygen ratio (C/O) is used to measure the distribution of fat and lean tissue in the body and to monitor small changes of lean mass. A sealed, D–T neutron generator is used for the production of fast neutrons. Carbon and oxygen mass and their ratio are measured in vivo at a radiation exposure of less than 0.06 mSv. Gamma-ray spectra are collected using large BGO detectors and analyzed for the 4.43 MeV state of carbon and 6.13 MeV state of oxygen, simultaneously with the irradiation. P and N analysis by delayed fast neutron activation is performed by transferring the patient to a shielded room equipped with an array of NaI(Tl) detectors. A combination of measurements makes possible the assessment of the quality of fat-free mass. The neutron generator system is used to evaluate the efficacy of new treatments, to study mechanisms of lean tissue depletion with aging, and to investigate methods for preserving function and quality of life in the elderly. It is also used as a reference method for the validation of portable instruments of nutritional assessment.     

Development of an LC-MS/MS method for the analysis of serotonin and related compounds in urine and the identification of a potential biomarker for attention deficit hyperactivity/hyperkinetic disorder

Serotonin is a major neurotransmitter and affects various functions both in the brain and in the rest of the body. It has been demonstrated that altered serotinergic function is implicated in various psychiatric disorders including depression and schizophrenia. Serotonin has also been implicated along with dopamine in attention deficit–hyperkinetic disorder (AD-HKD). This study provides a versatile validated method for the analysis of serotonin, hydroxyindole acetic acid and dopamine in urine using LC-MS/MS. This method was then used to quantify these analytes in a test group of 17 children diagnosed with severe AD-HKD. This group was compared to a matched control group to investigate the possibility that one of these compounds may be a potential biomarker for this condition. The developed method provided good linear calibration curves for the multiplex assay of analytes in urine (0.05–3.27 nmol/L; R ² ≥ 0.9977). Acceptable inter-day repeatability was achieved for all analytes with RSD values (n = 9) ranging from 1.1% to 9.3% over a concentration range of 0.11–3.27 μmol/L in urine. Excellent limits of detection (LOD) and limits of quantitation (LOQ) were achieved with LODs of 8.8–18.2 nmol/L and the LOQs of 29.4–55.7 nmol/L for analytes in urine. Recoveries were in the ranges of 98–104%, 100–106% and 91–107% for serotonin, 5-HIAA and dopamine, respectively. An appropriate sample clean-up procedure for urine was developed to ensure efficient recovery and reproducibility on analysis. Evaluation of matrix effects was also carried out and the influence of ion suppression on analytical results reported. Confirmatory analysis was carried out on a linear trap quadrupole-Orbitrap mass spectrometer to obtain high mass accuracy data of the target analytes in the clinical samples.     

Enhancement of intensities in glow discharge mass spectrometry by using mixtures of argon and helium as plasma gases

Glow discharge mass spectrometry (GD-MS) is an excellent technique for fast multi-element analysis of pure metals. In addition to metallic impurities, non-metals also can be determined. However, the sensitivity for these elements can be limited due to their high first ionization potentials. Elements with a first ionization potential close to or higher than that of argon, which is commonly used as discharge gas in GD-MS analysis, are ionized with small efficiency only. To improve the sensitivity of GD-MS for such elements, the influence of different glow-discharge parameters on the peak intensity of carbon, chlorine, fluorine, nitrogen, phosphorus, oxygen, and sulfur in pure copper samples was investigated with an Element GD (Thermo Fisher Scientific) GD-MS. Discharge current, discharge gas flow, and discharge gas composition, the last of which turned out to have the greatest effect on the measured intensities, were varied. Argon–helium mixtures were used because of the very high potential of He to ionize other elements, especially in terms of the high energy level of its metastable states. The effect of different Ar–He compositions on the peak intensity of various impurities in pure copper was studied. With Ar–He mixtures, excellent signal enhancements were achieved in comparison with use of pure Ar as discharge gas. In this way, traceable linear calibration curves for phosphorus and sulfur down to the μg kg⁻¹ range could be established with high sensitivity and very good linearity using pressed powder samples for calibration. This was not possible when pure argon alone was used as discharge gas. This contribution is based on a presentation given at the Colloquium for Analytical Atomic Spectroscopy (CANAS ’07) held March 18–21, 2007 in Constance, Germany.     

Determination of trace elements in zeolites by laser ablation ICP-MS

Laser ablation inductively coupled plasma mass spectrometry using a quadrupole-based mass spectrometer (LA-ICP-QMS) was applied for the analysis of powdered zeolites (microporous aluminosilicates) used for clean-up procedures. For the quantitative determination of trace element concentrations three geological reference materials, granite NIM-G, lujavrite NIM-L and syenite NIM-S, from the National Institute for Metallurgy (South Africa) with a matrix composition corresponding to the zeolites were employed. Both the zeolites and reference materials were fused with a lithium borate mixture to increase the homogeneity and to eliminate mineralogical effects. In order to compare two different approaches for the quantification of analytical results in LA-ICP-MS relative sensitivity coefficients (RSCs) of chemical elements and calibration curves were measured using the geostandards. The experimentally obtained RSCs are in the range of 0.2-6 for all elements of interest. Calibration curves for trace elements were measured without and with Li or Ti as internal standard element. With a few exceptions the regression coefficients of the calibration curves are better than 0.993 with internal standardization. NIM-G granite reference material was employed to evaluate the accuracy of the technique. Therefore, the measured concentrations were corrected with RSCs which were determined using lujavrite reference material NIM-L. This quantification method provided analytical results with deviations of 1–11% from the recommended and proposed values in granite reference material NIM-G, except for Co, Cs, La and Tb. The relative standard deviation (RSD) of the determination of the trace element concentration (n = 5) is about 1% to 6% using Ti as internal standard element. Detection limits of LA-ICP-QMS in the lower μg/g range (from 0.03 μg/g for Lu, Ta and Th to 7.3 μg/g for Cu, with the exception of La) have been achieved for all elements of interest. Under the laser ablation conditions employed (λ: 266 nm, repetition frequency: 10 Hz, pulse energy: 10 mJ, laser power density: 6 × 10⁹ W/cm²) fractionation effects of the determined elements relative to the internal standard element Ti were not observed. Received: 7 April 2000 / Revised: 25 May 2000 / Accepted: 31 May 2000     

Capillary electrophoresis–electrospray mass spectrometry and HR–ICP–MS for the detection and quantification of 10B-boronophenylalanine (10B–BPA) used in boron neutron capture therapy

Boron neutron capture therapy (BNCT) is a bimodal radiotherapeutic treatment based on the irradiation of neoplastic tissues with neutrons after the tissues have selectively accumulated molecules loaded with nuclides with large neutron capture cross-sections (such boron-10). Boron-10 carriers have been tested to a limited extent, and clinical trials have been conducted on sulfhydryl borane (¹⁰B-BSH) and boronophenylalanine (¹⁰B-BPA). However, precise and accurate measurements of boron-10 concentrations (0.1–100 μg/g) in specimens and samples of limited size (μg scale) are needed in order to be able to biologically characterise new compounds in predictive tissue dosimetry, toxicology and pharmacology studies as well as in clinical investigations. A new approach based on fast separation and detection of ¹⁰B-BPA performed by coupling capillary electrophoresis to electrospray mass spectrometry is reported. This method allows the quantitative analysis and characterisation of ¹⁰B-BPA in a short time with a high separation efficiency. Detection limits of 3 μM for ¹⁰B-BPA and 30 ng/mL for ¹⁰B were obtained with CE–ESI–MS. A quantification limit of 10 μM for ¹⁰B-BPA (100 ng/mL for ¹⁰B) was attained. The total boron-10 concentration was determined by high-resolution inductively coupled mass spectrometry in order to validate the method. Boron-10 isotope measurements were carried out by HR–ICP–MS at medium resolution (R=4000) due to the presence of an isobaric interference at mass 10. Good agreement was obtained between the values from CE–ESI–MS and those from HR–ICP–MS. The method has been successfully used to determine the ¹⁰B-BPA in two lines of cultured cells.     

Simultaneous analysis of vitamins and caffeine in energy drinks by surfactant-mediated matrix-assisted laser desorption/ionization

As a new approach to rapid small-molecule analysis, surfactant-mediated matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI–TOF-MS) was successfully used in the analysis of caffeine and the vitamins riboflavin, nicotinamide, and pyridoxine in various energy drinks. Of five common MALDI matrices tested (α-cyano-4-hydroxycinnamic acid, sinapinic acid, 2,5-dihydroxybenzoic acid, dithranol, and 2′,4′,6′-trihydroxyacetophenone), α-cyano-4-hydroxycinnamic acid was found to be most suitable for analysis of high-sugar-containing energy drinks. Cetyltrimethylammonium bromide (CTAB) surfactant was used as a matrix-ion suppressor, at a matrix:surfactant mole ratio of approximately 500:1. The resulting mass spectra show very few matrix-related ions, while analyte signals were clearly observed. For comparative purposes the same analytes were identified and quantified in energy drinks by LC–ESI–MS with UV detection. Quantitatively the calibration curves of all four analytes showed a marked improvement when the surfactant-mediated method was used compared with traditional MALDI–TOF-MS; correlation coefficients of 0.989 (nicotinamide), 0.991 (pyridoxine), 0.983(caffeine) and 0.987 (riboflavin) were obtained. It was found that in quantitation of the energy drink analytes the surfactant-mediated MALDI–TOF-MS results were comparable with those from LC analysis. In reproducibility experiments RSD values ranged from 9.7 to 18.1%. The work has demonstrated that this mass spectrometric approach can be used as a rapid screening technique for fortified drinks.     

Use of some organic dyes in gamma irradiation dose determination

In the present work, the radiation-induced color bleaching of Remazol brilliant blue (RBB), Wegocet orange (WO), Methyl green (Me G) and Thioflavine S (Th S) dyes solutions was studied. Solutions of these dyes in different solvents were found to obey Beer’s law within certain concentration levels. The % color bleaching occurring in different dye solutions on using different gamma irradiation doses was determined and the data obtained showed the existence of good linear relationships among them in the four dye systems used. The linear sections lines were used as calibration curves for evaluating unknown gamma irradiation doses. From the obtained results, it was concluded that RBB in water, WO in ethanol, Me G in butanol and Th S in 60% ethanol–water mixture could be used for dose evaluation within the dose ranges 5–25 kGy for RBB, 20–90 kGy for WO, 10–70 kGy for Me G and 5–160 kGy for Th S. The sensitivity of the systems towards gamma radiations has been also reported.     

Recent trends in trace element determination and speciation using inductively coupled plasma mass spectrometry

During the past decade, inductively coupled plasma mass spectrometry (ICPMS) has evolved from a delicate research tool, intended for the well-trained scientist only, into a more robust and well-established analytical technique for trace and ultra-trace element determination, with a few thousand of instruments used worldwide. Despite this immense success, it should be realized that in its ’standard configuration’– i.e. equipped with a pneumatic nebulizer for sample introduction and with a quadrupole filter – ICPMS also shows a number of important limitations and disadvantages: (i) the occurrence of spectral interferences may hamper accurate trace element determination, (ii) solid samples have to be taken into solution prior to analysis and (iii) no information on the ‘chemical form’ in which an element appears can be obtained. Self-evidently, efforts have been and still are made to overcome the aforementioned limitations to the largest possible extent. The application of a double focusing sector field mass spectrometer in ICPMS instrumentation offers a higher mass resolution, such that spectral overlap can be avoided to an important extent. Additionally, in a sector field instrument, photons are efficiently eliminated from the ion beam, resulting in very low background intensities, making it also very well-suited for extreme trace analysis. Also the combination of the ICP as an ion source and a quadrupole filter operated in a so-called ‘alternate’ stability region, an ion trap or a Fourier transform ion cyclotron resonance mass spectrometer allows high(er) mass resolution to be obtained. With modern quadrupole-based instruments, important types of spectral interferences can be avoided by working under ‘cool plasma’ conditions or by applying a collision cell. The use of electrothermal vaporization (ETV) or especially laser ablation (LA) for sample introduction permits direct analysis of solid samples with sufficient accuracy for many purposes. The application range of LA-ICPMS has become very wide and the introduction of UV lasers has led to an improved spatial resolution. Solid sampling ETV-ICPMS on the other hand can be used for some specific applications only, but accurate calibration is more straightforward than with LA-ICPMS. Limited multi-element capabilities, resulting from the transient signals observed with ETV or single shot LA, can be avoided by the use of a time-of-flight (TOF) ICPMS instrument. Finally, when combined with a powerful chromatographic separation technique, an ICP-mass spectrometer can be used as a highly sensitive, element-specific multi-element detector in elemental speciation studies. Especially liquid (HPLC-ICPMS) and – to a lesser extent – gas (GC-ICPMS) chromatography have already been widely used in combination with ICPMS. In speciation work, sample preparation is often observed to be troublesome and this aspect is presently receiving considerable attention. For GC-ICPMS, new sample pretreatment approaches, such as headspace solid phase microextraction (headspace SPME) and the purge-and-trap technique have been introduced. Also supercritical fluid chromatography (SFC) and capillary electrophoresis (CE) show potential to be of use in combination with ICPMS, but so far the application ranges of SFC-ICPMS and CE-ICPMS are rather limited. It is the aim of the present paper to concisely discuss the aforementioned recent ’trends’ in ICPMS, using selected real-life applications reported in the literature. Received: 30 November 1998 / Revised: 22 March 1999 / Accepted: 24 March 1999     

Application of ICP-MS for Multielement Analysis in Small Sample Amoun ts of Pathological Thyroid Tissue

 As a result of the Chernobyl nuclear power plant accident in 1986, thyroid pathologies occurred among children in some regions of Belarus. Besides the irradiation of children’s thyroids by radioactive iodine and caesium nuclides, toxic elements from fallout are a direct risk to health. Inductively coupled plasma quadrupole-based mass spectrometry was used for multielement determination in small amounts (1–10 mg) of thyroid tissue samples obtained during thyroid operations in Minsk hospitals. The accuracy of the applied analytical technique for small biological sample amounts was checked using NIST Standard Reference Material oyster tissue (SRM 1566b) and by comparison with independent analytical methods, such as neutron activation analysis. Almost all essential elements as well as a number of toxic elements such as Cd, Pb, Hg, U etc. were determined in a multitude of human and animal thyroid tissues (up to 1 mg sample material) by quadrupole-based ICP-MS using micronebulization. In general, the thyroid tissue affected by pathology is characterized by higher calcium content. Some other elements, among them Fe, Mn, V, As, Cr, Ni, Pb, U, Ba, Sb, were also accumulated in such tissue. The results obtained will be used as initial material for further specific studies of the role of particular elements in thyroid pathology development. Received November 15, 1999. Revision March 15, 2000.     

Effect of the functionalizing of carbon nanotubes on the electrodeposited catalysts’ structure and catalytic properties

The structure and hydrophilic-hydrophobic properties of functionalized single-wall carbon nanotubes are studied by the standard porosimetry method. It is shown that the functionalized nanotubes have highly hydrophilic surface; at that the summary surface area measured “by octane” decreased, as a result of the functionalizing, due to the blocking of the nanotubes’ inner channels by the functional groups located at the nanotubes’ ends. The nanotubes’ capacitive properties are studied; their charging-discharging curves appeared being highly reversible, unlike those of other carbonaceous materials. Catalytic properties of the functionalized nanotubes are studied, with particular tendency toward their using as a carrier of platinum catalysts for the methanol oxidation and oxygen electroreduction reactions. When minor amounts (5–10 μg cm⁻²) of platinum or platinum-ruthenium alloy are deposited onto the nanotubes’ hydrophilic surface, uniform layer of the catalyst is formed, with specific surface area up to 150–300 m² g⁻¹; high current of the methanol oxidation or oxygen electroreduction is observed at these catalysts. When the catalyst deposit mass increased, its specific surface area decreased, as well as the specific current of the reactions occurring thereon. When the current is related to the electrochemically active unit surface, the catalytic activity is nearly the same both for different catalyst mass deposited onto the nanotubes and the same catalyst mass at different carbonaceous carriers.     

TRIS (perfluoroalkylethyl)silyl alkyl amines as calibration standards for electron ionization mass spectrometry in the mass range of 100–3000 Da

A new fluorinated compound mixture has been developed for the calibration of the double focusing mass spectrometer in the mass range of 100–3000 Da in the positive electron ionization (EI) mode. Current calibration standards for EI have either limited mass range [perfluorotributylamine (PFTBA), perfluorokerosene (PFK), s-triazines (TRIS)] or poor peak intensities with significant chemical background in the instrument for several days (perfluoroalkyl phosphazine). The newly synthesized fluorinated silyl alkyl amines mixture is proposed as a reference/calibration standard for EI-MS. This standard produced abundant parent and fragment ions across the entire mass range without any memory effect.