Vapor Samples Research Articles

Triple Water Vapour–Isotopologues Record from Chhota Shigri, Western Himalaya, India: A Unified Interpretation based on δ17O, δ18O, δD and Comparison to Meteorological Parameters

The objective of this study is to investigate and understand the source and transportation of water vapour in the western Himalayan region—that is still missing—using water vapour stable isotopologues and air mass trajectory diagnostics. We report the first-time triple oxygen isotopic compositions of water vapour from high altitude western Himalaya (Chhota Shigri, India) and compare them with meteorological conditions at the site of investigation as well as tracked backwards through the Lagrangian air mass trajectory diagnostics. A total of 21 water vapour samples were collected using a quantitative cryogenic method. δ17O and δ18O values show a significant correlation coefficient of 0.999 (p <0.01). The temporal variations of δ17O, δ18O, δD, D-excess and 17O-excess are 1.2, 2.3, 17.3, 11.6 and 39‰ permeg, respectively. δ17O and δ18O exhibit significant (p < 0.05) diurnal variations along with meteorological parameters. Chhota Shigri vapour isotopic results show a clear difference in the 17O-excess value compared to near the south Indian Ocean and the Southern Ocean regions, reflecting the influence of local moisture recycling at the continental site. NCEP/NCAR reanalyses show lower Specific Humidity during the sampling period (September, ending month of the Indian summer monsoon) favouring evaporative conditions which are further corroborated through the Lagrangian moisture diagnostics suggesting frequent moisture uptake and moisture loss in specific regions.

Determination of the time-dependent change in the vapor concentration of 2,4,6-trinitrotoluene during the sublimation of its traces from the glass surface

The results of the measurements of 2,4,6-trinitrotoluene (TNT) vapor concentration over its trace amounts, called thin films, on the glass surface with a concentration of 100 ng/cm2 in a square area with a side of 1 cm over time are presented. The trace amounts of TNT on the glass were formed by applying a solution of TNT in the acetonitrile diluted with the chemically pure acetone, followed by the evaporation of the solvents. In order to measure the TNT vapor concentration, an EKHO-V-IDTS portable multibacillary gas-chromatograph with preliminary TNT vapor concentration was used. A sampling of the TNT vapor above the object was carried out with a remote vortex sampler. The vapor sample was taken from a distance of 2 cm from the glass surface. The concentration in the mode of the complete capture of TNT vapors was carried out to the stainless-steel wire mesh. The vapor concentration was determined from the chromatographic peak amplitude. It was found that the concentration of vapor over the examined surface with an area of 1 cm2 decreases from 10-13 to 10-14 g/cm3 within 2.6 ± 0.3 hours. TNT vapor concentration value of 10-14 g/cm3 corresponds to the threshold concentration of TNT vapor for the modern detectors. Based on the assumption that the vapor concentration is proportional to the amount of the TNT mass on the surface for the considered trace amounts of TNT, it was estimated that the initial surface concentration of trinitrotoluene of 100 ng/cm2 on the glass surface decreases to 12 ng/cm2 within 2.6 ± 0.3 hours due to sublimation into an open half-space. It was shown that the use of vortex sampling of vapor intensifies the sublimation of TNT from the glass surface.

Isothermal Evaporation Rate of Deposited Liquid Aerosols and the SARS-CoV-2 Coronavirus Survival

It is shown that the evaporation rate of a liquid sample containing the culture of coronavirus affects its survival on a substrate. Possible mechanisms of such influence can be due to the appearance of large, about 140 bar, non comprehensive capillary pressures and the associated dynamic forces during the movement of the evaporation front in a sample with the virus. A simulation of isothermal evaporation of a thin liquid sample based on the Stefan problem was performed. The comparison of simulation data and recent experiments on the coronavirus survival on various surfaces showed that the rate of isothermal evaporation of aqueous samples, which is higher for heat-conducting materials, correlates well with the lifetime of the coronavirus on these surfaces.

Аналіз неізотермічних процесів в дегазаторах ресорбційних холодильних машин

The aim of the article is to develop a method of calculations and analysis of the non-isothermal process of boiling the solution in countercurrent degassers of resorption refrigeration machines (RCM) at different variants of solution concentrations and vapor sampling temperatures. The concentration and properties of the solution change in the degasser in contrast to the flow of liquid or gas being cooled. Therefore, the results of the analysis predict the ability to choose the parameters of the solution and steam to equalize the temperature pressure between the cooling solution and the cooled stream, which will increase the thermodynamic efficiency of the RHM. According to the presented method, the analysis of the temperature dependence on the received heat for the solution of ammonia in water at boiling in the set temperature range is carried out. According to the constructed graphs, it is proved that this dependence is not proportional. The deviation from proportionality depends on the initial concentration of the solution. The largest deviation from proportionality corresponds to a high concentration of the solution. As the concentration of the solution decreases to the average value, the deviation from proportionality decreases. This is due to the fact that due to the unlimited solubility of ammonia in water and the different heat of vaporization of water and ammonia, the thermal properties of the solution change from a more ammonia-saturated solution to a less saturated one. Thus, to approximate the equidistance of the boiling solution to the stream being cooled, it is necessary to choose the initial concentration of the solution based on the analysis of this method. In addition, whenever possible, the components of the solution for RHM with similar thermal properties should be selected. The equidistance of the temperatures of the boiling solution to the cooled stream will increase the thermodynamic efficiency of the RHM. Thus, the developed technique allows analyzing the relationship between temperature and heat of the solution, the properties of which change during boiling. It is proved by the example of boiling a solution of ammonia in water that this dependence is disproportionate due to the change in the concentration of the solution. The deviation from proportionality is affected by the initial concentration of the solution, which must be chosen so as to approach the equidistance of changes in temperature of the cooling stream of the solution and the cooled stream of liquid or gas. This will increase the efficiency of RСM for their use in energy-saving technologies.

Non-contact detection of thiodiglycol vapors and associated degradation products using atmospheric flow tube mass spectrometry.

Thiodiglycol (TDG) is a synthetic precursor and an environmental degradation product of sulfur mustard (HD). Consequently, its presence can be indicative of illicit preparation or historical presence of chemical weapons, but its lower toxicity lends itself to use as an HD simulant for testing and method development. Detection of TDG vapor often proves elusive with existing techniques exhibiting undesirably high detection limits in the gas phase (>ppm). Moreover, traditional approaches to detecting TDG vapor rely upon non-specific approaches that do not provide the certainty afforded by mass spectrometry. Using atmospheric flow tube mass spectrometry (AFT-MS), which has previously demonstrated the capacity to detect parts-per-quadrillion levels of vapor, we evaluate the capacity of this approach for non-contact residue analysis based upon TDG vapor sampling and nitrate clustering chemistry. Furthermore, we discuss challenges with ambient vapor detection using the AFT-MS system and associated observations related to TDG degradation into 2,2'-sulfonyldiglycol from exposure to ambient conditions with vapor detection being possible even after 7-weeks of sample aging.

Combination of imine bond and samarium emitter enables turn-off fluorescence detection of hydrazine in vapor and water samples

The development of convenient and efficient fluorescence techniques is of great significance for selective detection and precise determination of biotoxic N2H4 in human health and environmental sciences. By the pre-organization-assisted template synthesis, disclosed here is a luminescent Sm(III) macrocycle-based probe Sm-2m bearing dynamic imine bonds as recognition moieties which provides the selective and ratiometric turn-off fluorescence sensing for N2H4 over various amine species based on the N2H4-induced structure transformation. This fluorescent sensing process finished within 20 min shows the low limit of detection (0.18 μM, 7.2 ppb) and wide linear sensing range (0–60.0 μM). Furthermore, probe Sm-2m is also be used to quantitatively determine N2H4 in vapor gas and water samples through fluorescence color changes, which are evaluated by the Sm-2m-impregnated test paper strips and RGB value outputs. Finally, our proposed smartphone-based analytical method gives satisfactory N2H4 detection results. It is thus believed that this work can shed some lights on development of optical probes and detection techniques for N2H4, even other hazardous chemicals.

Reusable Surface-Enhanced Raman Spectroscopy Membranes and Textiles via Template-Assisted Self-Assembly and Micro/Nanoimprinting.

Surface-enhanced Raman spectroscopy (SERS) has emerged as a powerful tool for ultrasensitive fingerprint recognition of molecules with considerable potential in wearable biochemical sensing. However, previous efforts to fabricate wearable SERS devices by directly treating fabrics with plasmonic nanoparticles have generated a nonuniform assembly of nanoparticles, weakly adsorbed on fabrics via van der Waals forces. Here, we report the creation of washing reusable SERS membranes and textiles via template-assisted self-assembly and micro/nanoimprinting approaches. Uniquely, we employ the capillary force driven self-assembly process to generate micropatch arrays of Au nanoparticle (NP) aggregates within hydrophobic microstructured templates, which are then robustly bonded onto semipermeable transparent membranes and stretchable textiles using the UV-resist based micro/nanoimprinting technique. A mild reactive ion etching (RIE) treatment of SERS membranes and textiles can physically expose the SERS hotspots of Au NP-aggregates embedded within the polymer UV resist for further improvement of their SERS performance. Also, we demonstrate that the semipermeable transparent SERS membranes can keep the moisture content of meat from evaporating to enable stable in situ SERS monitoring of biochemical environments at the fresh meat surface. By contrast, stretchable SERS textiles can allow the spreading, soaking, and evaporation of solution analyte samples on the fabric matrix for continuous enrichment of analyte molecules at the hotspots in biochemical SERS detection. Due to the mechanical robustness of the UV-resist immobilized Au NP aggregates, simple detergent-water washing with ultrasound sonication or mechanical stirring can noninvasively clean contaminated hot spots to reuse SERS textiles. Therefore, we envision that washing reusable SERS membranes and textiles by template-assisted self-assembly and micro/nanoimprinting fabrication are promising for wearable biochemical sensing applications, such as wound monitoring and body fluid monitoring.

Application of portable gas chromatography–mass spectrometer for rapid field based determination of TCE in soil vapour and groundwater

The application of portable chromatography–mass spectrometer (GC–MS) is restrained by its detection limits without the development of proper sample pre-concentration methods. The primary focus of this paper is to introduce a practical field measurement methodology for the analysis of volatile organic compounds (VOCs) in soil vapour and groundwater using a portable gas (GC–MS)system for application to in situ assessment of vapour intrusion from VOC contamination. A solid-phase micro-extraction (SPME) technique was applied for sample pre-concentration before the GC–MS​ measurement. Practical in-field soil gas SPME sampling methods have been developed to optimise the SPME extraction efficiency to then ultimately improve the detection limits of portable GC–MS. An Australian site impacted by a chlorinated VOC, trichloroethylene (TCE), was the subject of the case study. To rapidly assess soil vapour samples in subsurface soil, in-house-developed retractable soil vapour sampling probes (SVSPs) were installed at the site in clusters at depths of 1 m, 2 m and 3 m below ground level at each sampling location. Use of the SVSPs for sampling enabled the generation of a three-dimensional map and distribution contours for TCE concentrations using the in situ measurement results of a portable GC–MS analysis for vapour intrusion investigation. The results of the portable GC–MS​ analysis were compared with the results from conventional USEPA methods, such as TO-15 and Method 8265 for soil vapour and groundwater samples, respectively. This work demonstrates that the developed methodology of using a portable GC–MS system has the capability for in-field quantitative analysis of VOCs for rapid contaminated site vapour intrusion assessment.

Rapid Vapor-Collection Method for Vapor Pressure Measurements of Low-Volatility Compounds.

Dynamic vapor microextraction (DVME) is a new method that enables rapid vapor pressure measurements on large molecules with state-of-the-art measurement uncertainty for vapor pressures near 1 Pa. Four key features of DVME that allow for the rapid collection of vapor samples under thermodynamic conditions are (1) the use of a miniature vapor-equilibration vessel (the "saturator") to minimize the temperature gradients and internal volume, (2) the use of a capillary vapor trap to minimize the internal volume, (3) the use of helium carrier gas to minimize nonideal mixture behavior, and (4) the direct measurement of pressure inside the saturator to accurately account for overpressure caused by viscous flow. The performance of DVME was validated with vapor pressure measurements of n-eicosane (C20H42) at temperatures from 344 to 374 K. A thorough uncertainty analysis indicated a relative standard uncertainty of 2.03-2.82% for measurements in this temperature range. The measurements were compared to a reference correlation for the vapor pressures of n-alkanes; the deviation of the measurements from the correlation was ≤2.85%. The enthalpy of vaporization of n-eicosane at 359.0 K was calculated to be ΔvapH = 91.27 ± 0.28 kJ/mol compared to ΔvapH(corr) = 91.44 kJ/mol for the reference correlation. Total measurement periods as short as 15 min (3 min of thermal equilibration plus 12 min of carrier gas flow) were shown to be sufficient for high-quality vapor pressure measurements at 364 K.

English

Indole-3-acetic acid (IAA) is an important plant growth regulator. As the very first endeavor, the study is aimed at extracting and quantifying IAA from seedlings of Bambusa tulda and evaluating its bioactivity. The extraction of IAA was performed in organic solvent followed by sample evaporation and TLC with a mobile phase composed of chloroform, methanol and formic acid (77:22:1 v/v) in isocratic mode. The extract obtained from preparatory TLC was subjected to HPLC with acetic acid and methanol (75:25 v/v) as the mobile phase in isocratic mode at a flow rate of 0.8 ml/min and operation pressure of 54 MPa at 30°C, and detection was monitored at 280 nm. Bioassay of the extracted IAA was carried out in Abelmoschus esculentus seedlings. The similar Rf value (0.412) of the extract during TLC analysis and similar peak of HPLC chromatogram with retention time 28.71 min to that of standard IAA indicated the presence of IAA in B. tulda seedling extract. The extracted IAA was quantified to be 10.28 µg/ml. In bioassay experiment, the extracted IAA significantly enhanced root length, root fresh weight, root dry weight, shoot length, shoot fresh weight, shoot dry weight and significant increase of total chlorophyll and protein in A. esculentus leaves. Therefore, B. tulda seedlings could be a potential source of IAA, and it can be utilized for production of bio-fertilizer at a commercial scale. Key words: Abelmoschus esculentus, Bamboo, High performance liquid chromatography, indole-3 acetic acid.

A paper-based colorimetric sensor array for discrimination of monofloral European honeys based on gold nanoparticles and chemometrics data analysis.

A sensitive and simple nanomaterial based colorimetric sensor array (NBCSA) was developed for discrimination of monofloral honey from various European countries based on three botanical origins as Acacia, Canola and Honeydew. The NBCSA was designed by spotting gold (AuNPs) and silver (AgNPs) nanoparticles synthesized using six different reducing and/or capping agents. The colour intensity of AuNPs represented differential changes when interacting with volatile organic compounds appeared in the headspace of the honey samples. The color difference maps, which are calculated as the difference between color intensity of the sensor before and after exposing to the sample vapors, were used as a fingerprint to discriminate the honey samples based on botanical origin. Classification was achieved utilizing data pre-processing and chemometrics data analysis. Fitting accuracies of 88% and 86% were obtained by partial least squares discriminant analysis and linear discriminant analysis whereas 100% was achieved using support vector machine.

Craig–Gordon model validation using stable isotope ratios in water vapor over the Southern Ocean

Abstract. The stable oxygen and hydrogen isotopic composition of water vapor over a water body is governed by the isotopic composition of surface water and ambient vapor, exchange and mixing processes at the water–air interface, and the local meteorological conditions. These parameters form inputs to the Craig–Gordon models, used for predicting the isotopic composition of vapor produced from the surface water due to the evaporation process. In this study we present water vapor, surface water isotope ratios and meteorological parameters across latitudinal transects in the Southern Ocean (27.38–69.34 and 21.98–66.8∘ S) during two austral summers. The performance of Traditional Craig–Gordon (TCG) (Craig and Gordon, 1965) and the Unified Craig–Gordon (UCG) (Gonfiantini et al., 2018) models is evaluated to predict the isotopic composition of evaporated water vapor flux in the diverse oceanic settings. The models are run for the molecular diffusivity ratios suggested by Merlivat (1978), Cappa et al. (2003) and Pfahl and Wernli (2009), referred to as MJ, CD and PW, respectively, and different turbulent indices (x), i.e., fractional contribution of molecular vs. turbulent diffusion. It is found that the UCGx=0.8MJ, UCGx=0.6CD, TCGx=0.6MJ and TCGx=0.7CD models predicted the isotopic composition that best matches with the observations. The relative contribution from locally generated and advected moisture is calculated at the water vapor sampling points, along the latitudinal transects, assigning the representative end-member isotopic compositions, and by solving the two-component mixing model. The results suggest a varying contribution of the advected westerly component, with an increasing trend up to 65∘ S. Beyond 65∘ S, the proportion of Antarctic moisture was found to be prominent and increasing linearly towards the coast.

Full “Ab-Initio” Simulation of Field Evaporation of Samples with Grain Boundaries

Full “Ab-Initio” Simulation of Field Evaporation of Samples with Grain Boundaries

Experiments for observation of self-similar effects in water vapor near saturation pressure at room temperature

The simple setup was realized to analyze samples of water vapor collected from the solid surface adsorbent in the form of corundum ceramic balls. The adsorbent was previously saturated with water vapor from a source of distilled liquid water without dissolved gases. Testing of samples is carried out in a glass vessel isolated from the adsorbent by means of a forced change of pressure of vapor in the vessel. The necessary pressure rise occurs at the moment when steam is let into the vessel and the pressure drops during the vacuum pumping of water vapor. It was found that the samples respond differently to the rate of pressure change. This characteristic of gaseous mediums is associated with a significant quantity of discharged water molecules. It was found that the tested samples are clearly divided into two types according to the rate of pressure change. The first few samples behave in a similar way, but the behavior of the remaining samples is very different. It depends on the serial number of the sample. Samples demonstrate the self-similarity effect at the final stage of the experiment. In this case the rate of change of pressure smoothly decreases to a value of 3/4. This study found that the properties of water vapor can change during desorption from the adsorbent, in contrast to the current view that all desorbed water molecules are identical in their properties.

(Mono-) Exposure to Naphthalene in the Abrasives Industry: Air Monitoring and Biological Monitoring.

Exposure to the bicyclic aromatic hydrocarbon naphthalene occurs in most cases along with other polycyclic aromatic hydrocarbons. Here we report from an investigation of 63 healthy, non-smoking male employees in the abrasives industry where naphthalene is the only relevant chemical exposure. Exposure assessment was performed using a combination of Air and Biological Monitoring over nearly a whole working week (Mo.-Th.). Air measurements were carried out during the shift on Thursday with the GGP mini-sampling system, combining particle and vapour sampling at low flow rates. In urine spot samples, the metabolites 1- and 2-naphthol were measured Mo.-Th. pre- and post-shift (for the reference group only Mo. pre- and Th. post-shift). With regard to naphthalene concentrations measured in air and concentrations of its metabolites (1- and 2-naphthol) in urine, study participants could be divided into a high and a low exposure group, and a reference group. The naphthalene concentration in air was in the range of 0.1-11.6 mg m-3, and naphthol concentrations (sum of 1- and 2-naphthol) in post-shift urine were in the range of <1 to 10 127 µg l-1. Naphthalene concentrations in air and naphthol concentrations in urine were closely correlated, indicating mainly airborne exposure at the investigated workplaces. As expected from toxicokinetic data, internal body burden increased slightly during a working week and did not completely decline over a work-free weekend to background concentrations observed in occupationally not exposed persons. Taking into account the observed increase in pre- and post-shift values during the working week, urine sampling for Biological Monitoring at workplaces should be carried out after several preceding shifts. Our data allow the derivation of biological limit values for the sum of 1- and 2-naphthol in urine corresponding to occupational exposure limits for naphthalene in air.

Fabrication, Characterization and Optical Investigation of Semi-organic Nonlinear Alanine Hippurate Single Crystals

In the present work, a single crystal of alanine and hippuric acid was prepared through the slow growth dynamics of sample evaporation. The crystallinity, structure, and cell parameters of the produced single crystals were determined by X-ray diffraction (XRD) analysis. While, frequency shifting and the various functional groups of alanine with hippuric acid were investigated by FTIR and FT-Raman studies. In addition, grain size and the morphological shape of alanine hippurate (AH) single crystals were examined by FE-SEM analysis. Transmission of light through the grown material was defined by UV-VIR-NIR study. Moreover, mechanical stability of the grown single crystals was analyzed with Vicker’s microhardness tester. Melting point and thermal stability were tested through TGA, DGA, and DSC investigations. Our results explored that, the prepared single crystals exhibited high-grade transparency and lower cut-off wavelength of about 300 nm. UV–VIS–NIR absorption spectrum revealed that there was less absorption in the visible region, and an emission peak at 574 nm was observed confirming the green emission of the prepared crystals. Interestingly, microhardness investigation showed that our single crystals belonged to the category of soft materials. While, thermal studies investigated the prepared crystals were stable up to 290 °C. Finally, the recorded SHG performance was 1.26 times that of KDP.

Rapid Capture and Extraction of Sweat for Regional Rate and Cytokine Composition Analysis Using a Wearable Soft Microfluidic System

Rapid Capture and Extraction of Sweat for Regional Rate and Cytokine Composition Analysis Using a Wearable Soft Microfluidic System

Cryo-EM structures from sub-nl volumes using pin-printing and jet vitrification

The increasing demand for cryo-electron microscopy (cryo-EM) reveals drawbacks in current sample preparation protocols, such as sample waste and lack of reproducibility. Here, we present several technical developments that provide efficient sample preparation for cryo-EM studies. Pin printing substantially reduces sample waste by depositing only a sub-nanoliter volume of sample on the carrier surface. Sample evaporation is mitigated by dewpoint control feedback loops. The deposited sample is vitrified by jets of cryogen followed by submersion into a cryogen bath. Because the cryogen jets cool the sample from the center, premounted autogrids can be used and loaded directly into automated cryo-EMs. We integrated these steps into a single device, named VitroJet. The device’s performance was validated by resolving four standard proteins (apoferritin, GroEL, worm hemoglobin, beta-galactosidase) to ~3 Å resolution using a 200-kV electron microscope. The VitroJet offers a promising solution for improved automated sample preparation in cryo-EM studies.

Fabrication of high-strength Mg-Gd-Zn-Zr alloy via selective laser melting

A Mg-11.00Gd-1.77Zn-0.43Zr (wt.%) alloy named GZ112K was prepared by selective laser melting (SLM) with different processing parameters. The formability, element vaporization, microstructure and tensile properties of the SLMed samples at different scanning speed and hatch spacing were characterized. The process map at a constant laser power of 80 W for the alloy has been established. It shows that the optimum scanning speed and hatch spacing are 300–700 mm/s and 100 μm respectively. The SLMed samples have fine grains of about 2 μm and dispersed eutectic phase of β-(Mg,Zn)3Gd due to the very high cooling rate, high solid solubility of Gd and Zn elements in ɑ-Mg matrix owing to the effect of solute trapping. The SLMed GZ112K alloy with scanning speed of 300 mm/s and hatch spacing of 100 μm has yield strength (YS) of 325 MPa, ultimate tensile strength (UTS) of 332 MPa and elongation of 4.0% at room temperature. Compared with as-cast alloy, the SLMed GZ112K alloy has much higher YS (+162 MPa), UTS (+122 MPa) and comparable elongation (+0.4%).

Olfactory Atlases with an Array of Porphyrinoids Coated ZnO Nanoparticle

Olfactory Atlases with an Array of Porphyrinoids Coated ZnO Nanoparticle