Testing of the spectroscopic method for location of water microleakages in ITER at the L-2M stellarator

Results of testing of a possible method for location of water microleakages in the cooling system of the first wall and vacuum chamber of ITER are presented. The method consists in spectroscopic detection of the emission lines of atoms and ions of the Xe additive dissolved in water. These lines are excited when the water with dissolved Xe contacts the plasma. The high electron cyclotron resonance heating (ECRH) power deposited in a relatively small plasma volume in the L-2M stellarator (P = 0.5 MW, V = 0.24 m³, and the specific heating power ??2 MW/m³) makes it possible to achieve plasma parameters close to those in the edge plasma of ITER for different operating modes, including the H-mode with an edge transport barrier. In test experiments, several lines of Xe ions were revealed suitable for detection of xenon in plasma with parameters close to those in the edge plasma of ITER at leakage rates at a level of ??10^?6 Pa m³ s^?1 and spatial resolution of ??0.5 cm.     

Measurements and monitoring of the hydrogen and deuterium contents in the plasma of the L-2M stellarator

The program of experiments on ITER includes a sequential change of the plasma isotopic composition from pure hydrogen plasma in the initial stage of research to deuterium and, then, deuterium-tritium plasma with a gradual increase in the tritium content. In this context, the influence of the plasma isotopic composition on the processes of plasma heating and confinement are being actively studied on the existing tokamaks and stellarators. The plasma isotopic composition also depends on the composition of the gas desorbed from the vacuum chamber wall in the course of recycling. Therefore, the rate of change of the plasma isotopic composition after altering the injected gas also depends on the rate of change of the isotopic composition of the gas absorbed in the wall. These effects were studied in the experiments carried out on the L-2M stellarator in which the working gas was changed from hydrogen to deuterium. Spectral measurements of the intensity ratio between the H _α and D _α lines made it possible to monitor the isotopic composition of the plasma in the course of cleaning of the chamber wall from earlier absorbed hydrogen and its replacement with deuterium. After returning to hydrogen, the rate of cleaning of the wall from deuterium was also determined. The results of these experiments show that the plasma isotopic composition varies exponentially with the number N of shots after transition to another isotope, ∼exp(−N/47). Hence, the isotopic composition can be changed almost completely over 2 to 3 working days. This allows one to study the influence of the plasma isotopic composition on plasma confinement during the same experimental session.     

Modeling of the feedback stabilization of the resistive wall modes in a tokamak

The problem of feedback stabilization of the resistive wall modes (RWMs) in a tokamak is discussed. An equilibrium configuration with the parameters accepted for the stationary ITER scenario 4A is considered as the main scenario. The effect of the vacuum chamber's shape on the plasma stability is studied. Ideal MHD stability is analyzed numerically by using the KINX code. It is shown that, in a tokamak with the parameters of the designed T-15M tokamak, RWMs can be stabilized by a conventional stabilizing system made of framelike coils. However, the maximum possible gain in β in such a tokamak is found to be smaller than that in ITER. It is shown that, in this case, a reduction in the plasma—wall gap width by 10 cm allows one to substantially increase the β limit, provided that RWMs are stabilized by active feedback.     

Analysis of biological samples using prompt gamma radions induced by 14.7-MeV neutrons

We investigate a method for determining the elemental composition of biological samples that uses prompt gamma rays induced by 14.7-MeV neutrons. Alpha particles are produced simultaneously with the neutrons, which exit opposite the alpha detector through the vacuum chamber wall. The sample under investigation is irradiated and emits gamma radiations in a spectral energy distribution characteristic of the material. Barium-fluoride (BaF₂) and high-purity germanium (HPGe) gamma detectors view the sample and record the spectrum of gamma radiation.

     

Experimental verification of the method for detection of water microleakages in plasma vacuum chambers by using the hydroxyl spectrum

Experimental determination of the sensitivity of the method for detection of water microleakages in the cooling systems of the plasma vacuum chambers of complex electrophysical devices (such as tokamaks, fuel elements of nuclear reactors, and plasmachemical reactors) is considered. It was shown that the spectroscopic method for detection of water microleakages by using the hydroxyl radiation spectrum makes it possible to detect leakages at a level of 10⁻⁵ Pa m³ s⁻¹. The spatial resolution of the method allows one to localize defects with an accuracy of several centimeters.     

Hydrogen lines in the infrared region and spectral background for the thomson scattering diagnostics of the iter divertor plasma

Calculations are made of the plasma spectral background, which is important for the Thomson scattering diagnostics in the ITER divertor. Theoretical grounds have been elaborated for computing the hydrogen spectral line shapes in the infrared spectral region for a divertor plasma in ITER. The shape of the P-7 Paschen line (transition n = 7 → n = 3) located near the laser scattering signal has been calculated for various lines of sight in the ITER divertor. Contributions from different mechanisms of broadening the P-7 line have been examined. The spectral intensities of bremsstrahlung and photorecombination continuum have been calculated. All calculations use data on the spatial distribution of temperatures and densities of all species of plasma particles computed with the SOLPS4.3 code for basic operation regimes of the ITER divertor.     

Changes in micropore system of roots of wheat and triticale seedlings under aluminum stress as determined using water vapor adsorption—desorption

Plant root structure including the pore system is severely injured in Al-toxic environments. Experimental water vapor desorption isotherms estimated using vacuum chamber method were used to characterize micropore build-up of roots of wheat (Lanca) and triticale (Debo) 4-day seedlings and its changes after 24 h (8 mg dm⁻³) aluminum stress. The micropore volumes and average pore radii increased after the stress whereas pore fractal dimensions decreased. The above changes were more pronounced for these roots which were not able to grow further after the stress when compared to the control roots, the total micropore volume was almost twice higher and the fractal dimension reached a value of 2 which is characteristic for flat, two-dimensional surface. The observed alterations of pore system indicate damage of root tissue and possible strong binding of aluminum on cell wall surfaces.     

A direct immunoassay for detecting diatoms in groundwater as an indicator of the direct influence of surface water

Groundwater under the direct influence of surface water (GWUDISW) is of concern in communities where growing public demand on groundwater resources has resulted in increased withdrawals and hydraulic stress near surface water bodies. Under these conditions, contaminants such as methyl-tert butyl ether (MTBE) and biological materials have been detected in domestic wells. Other contaminants and pathogens associated with surface water are not routinely tested for in groundwater-supplied systems. To address the need for methods to easily identify potentially vulnerable supplies, a direct immunoassay for the quantitative detection of diatoms in raw water samples was developed as a measure of surface water influence on groundwater. Cell wall preparations from Nitzschia palea Kützing, a freshwater diatom found throughout North America, were used to produce a polyclonal antibody that was applied in a direct enzyme-linked immunosorbent assay (ELISA) developed to detect the presence of N. palea cell wall components. The direct immunoassay allows detection at 500 cells L⁻¹, a level similar to diatom concentrations observed in samples of groundwater collected near the test site. This investigation was the first attempt to utilize an ELISA as an indicator of surface water influence on groundwater. Further research is needed to develop more specific diatom-based monoclonal antibodies, determine cross-reactivity, and optimize sample processing and ELISA procedures for development of a standardized method.     

A portable chamber for measuring algal primary production in streams

This paper describes a portable chamber that measures net primary production of stream periphyton using a ¹⁴C uptake method. The unique feature is that substrates are moved through water at a velocity of 20 cm s ⁻¹ rather than moving water over substrates. The chamber consists of a plexiglass cylinder that is 9 cm in height and 15 cm in diameter. On the top of the cylinder is a DC gearmotor powered by a 12 volt, deep cycle, marine battery. The motor turns a shaft that rotates a 13.3 cm plexiglass plate at a velocity of 20 cm s ⁻¹ . Small tiles (3.2 cm × 3.2 cm × 0.5 cm) that have natural algal assemblages are mounted on the rotating plate. After adding 500 ml of filtered stream water and 185 kBq (5 μCi) NaH¹⁴CO₃ to the chamber, the chambers are placed along a stream margin for 5 h. Measurements of ¹⁴C uptake by algae on the tiles provide estimates of net primary production (NPP). To assess the sensitivity and practicality of the chamber, algal primary production was measured in open and closed canopy sections of Kingsley Creek, Randallsville, New York. In autumn, primary production was higher in the open than closed canopy section and NPP was lower in spring in both sections probably because of scouring of algae due to snowmelt.     

Method for the analysis of the methylphosphonic acid metabolites of sarin and its ethanol-substituted analogue in urine as applied to the victims of the Tokyo sarin disaster

An analysis method for the methylphosphonic acid metabolites of sarin in urine using trimethylsilyl derivatization and flame photometric detection is described in this report. Authentic reference standards of isopropyl methylphosphonic acid (IMPA) and ethyl methylphosphonic acid (EMPA) as well as methylphosphonic acid were employed to estimate the concentration in human urine. A sample pretreatment procedure was developed for urine using a column of cation-loaded ion-exchange resins (Ag⁺-, Ba²⁺- or H⁺-Dowex) and adjusting the pH of the eluate from the column to 3.75–3.85 improved recovery of the target compounds. The eluate was evaporated to dryness under vacuum prior to trimethylsilylation, to remove water and any hydroxy- or amino-carrying volatile substances. The sarin metabolites, because of their low volatility, were concentrated and could be derivatized for analysis. The use of synthesized authentic sarin and ethylsarin metabolites, i.e., IMPA and EMPA, made it possible to establish the necessary sample pretreatment procedures for derivatization and gas chromatography–flame photometric detection (GC–FPD) analysis. The detection limits were 0.025 ppm both for EMPA and IMPA, and 0.625 μM for MPA, respectively. This method can be useful for estimating the exposure level to sarin by assaying the metabolites in urine and it is applicable to a large numbers of samples.     

Precise detection of pH inside large unilamellar vesicles using membrane-impermeable dendritic porphyrin-based nanoprobes

Accurate real-time measurements of proton concentration gradients are pivotal to mechanistic studies of proton translocation by membrane-bound enzymes. Here we report a detailed characterization of the pH-sensitive fluorescent nanoprobe Glu³, which is well suited for pH measurements in microcompartmentalized biological systems. The probe is a polyglutamic porphyrin dendrimer in which multiple carboxylate termini ensure its high water solubility and prevent its diffusion across phospholipid membranes. The probe’s pK is in the physiological pH range, and its protonation can be followed ratiometrically by absorbance or fluorescence in the ultraviolet-visible spectral region. The usefulness of the probe was enhanced by using a semiautomatic titration system coupled to a charge-coupled device (CCD) spectrometer, enabling fast and accurate titrations and full spectral coverage of the system at millisecond time resolution. The probe’s pK was measured in bulk solutions as well as inside large unilamellar vesicles in the presence of physiologically relevant ions. Glu³ was found to be completely membrane impermeable, and its distinct spectroscopic features permit pH measurements inside closed membrane vesicles, enabling quantitative mechanistic studies of membrane-spanning proteins. Performance of the probe was demonstrated by monitoring the rate of proton leakage through the phospholipid bilayer in large vesicles with and without the uncoupler gramicidin present. Overall, as a probe for biological proton translocation measurements, Glu³ was found to be superior to the commercially available pH indicators.     

Single-Molecule TPM Studies on the Conversion of Human Telomeric DNA

Human telomere contains guanine-rich (G-rich) tandem repeats of single-stranded DNA sequences at its 3′ tail. The G-rich sequences can be folded into various secondary structures, termed G-quadruplexes (G4s), by Hoogsteen basepairing in the presence of monovalent cations (such as Na⁺ and K⁺). We developed a single-molecule tethered particle motion (TPM) method to investigate the unfolding process of G4s in the human telomeric sequence AGGG(TTAGGG)₃ in real time. The TPM method monitors the DNA tether length change caused by formation of the G4, thus allowing the unfolding process and structural conversion to be monitored at the single-molecule level. In the presence of its antisense sequence, the folded G4 structure can be disrupted and converted to the unfolded conformation, with apparent unfolding time constants of 82 s and 3152 s. We also observed that the stability of the G4 is greatly affected by different monovalent cations. The folding equilibrium constant of G4 is strongly dependent on the salt concentration, ranging from 1.75 at 5 mM Na⁺ to 3.40 at 15 mM Na⁺. Earlier spectral studies of Na⁺- and K⁺-folded states suggested that the spectral conversion between these two different folded structures may go through a structurally unfolded intermediate state. However, our single-molecule TPM experiments did not detect any totally unfolded intermediate within our experimental resolution when sodium-folded G4 DNA molecules were titrated with high-concentration, excess potassium ions. This observation suggests that a totally unfolding pathway is likely not the major pathway for spectral conversion on the timescale of minutes, and that interconversion among folded states can be achieved by the loop rearrangement. This study also demonstrates that TPM experiments can be used to study conformational changes in single-stranded DNA molecules.     

A spectrophotometric method for the determination of zinc, copper, and cobalt ions in metalloproteins using Zincon

Zincon (2-carboxy-2′-hydroxy-5′-sulfoformazylbenzene) has long been known as an excellent colorimetric reagent for the detection of zinc and copper ions in aqueous solution. To extend the chelator’s versatility to the quantification of metal ions in metalloproteins, the spectral properties of Zincon and its complexes with Zn²⁺, Cu²⁺, and Co²⁺ were investigated in the presence of guanidine hydrochloride and urea, two common denaturants used to labilize metal ions in proteins. These studies revealed the detection of metals to be generally more sensitive with urea. In addition, pH profiles recorded for these metals indicated the optimal pH for complex formation and stability to be 9.0. As a consequence, an optimized method that allows the facile determination of Zn²⁺, Cu²⁺, and Co²⁺ with detection limits in the high nanomolar range is presented. Furthermore, a simple two-step procedure for the quantification of both Zn²⁺ and Cu²⁺ within the same sample is described. Using the prototypical Cu²⁺/Zn²⁺-protein superoxide dismutase as an example, the effectiveness of this method of dual metal quantification in metalloproteins is demonstrated. Thus, the spectrophotometric determination of metal ions with Zincon can be exploited as a rapid and inexpensive means of assessing the metal contents of zinc-, copper-, cobalt-, and zinc/copper-containing proteins.     

Radiometric Method for the Detection of Coliform Organisms in Water

A new radiometric method for the detection of coliform bacteria in water has been described. The method is based on the release of ¹⁴CO₂ from [¹⁴C]lactose by bacteria suspended in growth medium and incubated at 37 C. The evolved ¹⁴CO₂ is trapped by hyamine hydroxide and counted in a liquid scintillation spectrometer. The method permits the detection of 1 to 10 organisms within 6 h of incubation. Coliform bacteria suspended in water for several days recover from starvation and may be quantitated by the proposed method. Bacteria from water samples may also be concentrated by filtration through membrane filters and detected by the radiometric assay.     

A vacuum benthos sampler suitable for diverse habitats

The vacuum benthos sampler consists of a vacuum chamber equipped with a collecting net connected to the intake of a 12 volt pump, a battery, and a standpipe. Contents of the standpipe are vacuumed while substrate is removed and washed with the exhaust hose. The vacuum chamber is designed for rapid changing of nets during replicate sampling. This sampler is equally efficient in flowing and standing water. It was more effective than a modified Hess sampler for collecting a large variety of benthos from flowing (ca 0.25–0.75 m/s) riffles. Required operation time is variable, but 93% of invertebrates caught in 10 min were captured in the first 5 min during our tests, and there was a 94% mean recovery of released organisms during 10 min of subsequent operation. Advantages over previous suction samplers include interception of organisms before they pass through a pump, return of outlet water to the standpipe, capability of sampling in shallow (20–30 mm) water, and that it can be carried and operated by one person.     

Cleaning of inner vacuum surfaces in the Uragan-3M facility by radio-frequency discharges

A method for cleaning vacuum surfaces by a low-temperature (T _e ～ 10 eV) relatively dense (n _e ≈ 10¹² cm^?3) plasma of an RF discharge was developed and successfully applied at the Uragan-3M torsatron. The convenience of the method is that it can be implemented with the same antenna system and RF generators that are used to produce and heat the plasma in the operating mode and does not require retuning the frequencies of the antennas and RF generators. The RF discharge has a high efficiency from the standpoint of cleaning vacuum surfaces. After performing a series of cleanings by the low-temperature RF discharge plasma (about 20000 pulses), (i) the intensity of the CIII impurity line was substantially reduced, (ii) a quasi-steady operating mode with a duration of up to 50 ms, a plasma density of n _e ≈ 10¹² cm^?3, and an electron temperature of up to T _e ～ 1 keV was achieved, and (iii) mass spectrometric analysis of the residual gas in the chamber indicated a significant reduction in the impurity content.     

Growth and photosynthesis of soybean (Glycine max (L.) Merr.) in simulated vegetation shade: influence of the ratio of red to far-red radiation*

Abstract. Glycine max (L.) Merr. was grown under several light conditions to determine the role of red and far-red radiation in plant adaptation to vegetation shade. Neutral density,‘neutral’ density with elevated far-red radiation, and green shade treatments were used in a greenhouse, producing calculated phytochrome photostationary state (P_fr/P_r+P_fr) values of 0.68, 0.63 and 0.51, respectively. Cool-white fluorescent lamps either alone or in conjunction with far-red fluorescent lamps were used in a growth chamber, providing P_fr/P_r+P_fr of 0.79 and 0.61, respectively. Daily photo-synthetically active radiation was about 25% of daylight and was approximately equal for both greenhouse (2.15MJ m^?2) and growth chamber (2.57MJ m^?2). Developmental stage 4 weeks after sowing was similar for all treatments, but axillary growth and rates of leaf area and dry matter accretion differed between plants from greenhouse and growth chamber. Light conditions simulating vegetation shade (i.e. a low ratio of red to far-red radiation) significantly promoted petiole elongation and retarded the rate of stem elongation in both greenhouse and growth chamber experiments. Other aspects of growth either were not significantly altered by spectral quality or were not modified consistently in both greenhouse and growth chamber environments. Net photosynthetic rates measured under growth conditions for unifoliate and first trifoliolate (TF₁) leaves of growth chamber plants between 9 and 21 d after sowing were generally unaffected by spectral quality, but supplemental FR enhanced TF₁ leaf area expansion. The latter effect was not correlated with increased dry matter accumulation. The significance of spectral quality for adaptation of soybeans to canopy closure and intercropping is discussed.     

Effects of gel processing on the properties of humic acid isolated from the alga Pilayella littoralis: A humic acid aerogel

Humic acid in the live alga Pilayellalittoralis was isolated as an aqueous gel by a standard sequential extraction method augmented with removal of alginic acid. Portions of the aqueous gel were (1) vacuum oven dried at 40 °C, (2) freeze freeze dried after cooling in liquid N₂, and (3) dried with supercritical fluid CO₂ after substitution of water in the gel with acetone. This paper compares the analytical and spectral properties of the products with compost derived HA and reports significant differences in their surface areas, packing densities, water retention, solute sorption and metal binding properties. The results are discussed in terms of different product morphologies determined by scanning electron microscopy. The aerogel obtained by supercritical fluid CO2 drying of an HA gel from Pilayella has the highest surface area (188 m² g^-1) reported for a humic acid. This revised version was published online in August 2006 with corrections to the Cover Date.     

Rapid culture-based detection of Legionella pneumophila using isothermal microcalorimetry with an improved evaluation method

The detection and quantification of Legionella pneumophila (responsible for legionnaire's disease) in water samples can be achieved by various methods. However, the culture-based ISO 11731:2017, which is based on counts of colony-forming units per ml (CFU·ml^-1) is still the gold standard for quantification of Legionella species (spp.). As a powerful alternative, we propose real-time monitoring of the growth of L. pneumophila using an isothermal microcalorimeter (IMC). Our results demonstrate that, depending on the initial concentration of L. pneumophila, detection times of 24–48 h can be reliably achieved. IMC may, therefore, be used as an early warning system for L. pneumophila contamination. By replacing only visual detection of growth by a thermal sensor, but otherwise maintaining the standardized protocol of the ISO 11731:2017, the new procedure could easily be incorporated into existing standards. The exact determination of the beginning of metabolic heat is often very difficult because at the beginning of the calorimetric signal the thermal stabilization and the metabolic heat development overlap. Here, we propose a new data evaluation based on the first derivation of the heat flow signal. The improved evaluation method can further reduce detection times and significantly increase the reliability of the IMC approach.     

First-principles study of water desorption from montmorillonite surface

Knowledge about water desorption is important to give a full picture of water diffusion in montmorillonites (MMT), which is a driving factor in MMT swelling. The desorption paths and energetics of water molecules from the surface of MMT with trapped Li⁺, Na⁺ or K⁺ counterions were studied using periodic density functional theory calculations. Two paths—surface and vacuum desorption—were designed for water desorption starting from a stationary structure in which water bonds with both the counterion and the MMT surface. Surface desorption is energetically more favorable than vacuum desorption due to water–surface hydrogen bonds that help stabilize the intermediate structure of water released from the counterion. The energy barriers of water desorption are in the order of Li⁺?>?Na⁺?>?K⁺, which can be attributed to the short ionic radius of Li⁺, which favors strong binding with the water molecule. The temperature dependence of water adsorption and desorption rates were compared based on the computed activation energies. Our calculations reveal that the water desorption on the MMT surface has a different mechanism from water adsorption, which results from surface effects favoring stabilization of water conformers during the desorption process.