Gas Phase Standards Research Articles

Demonstrating the Applicability of Proton Transfer Reaction Mass Spectrometry to Quantify Volatiles Emitted by the Mycoparasitic Fungus Trichoderma atroviride in Real Time: Monitoring of Trichoderma-Based Biopesticides.

The present study aims to explore the potential application of proton transfer reaction time-of-flight mass spectrometry (PTR-ToF-MS) for real-time monitoring of microbial volatile organic compounds (MVOCs). This investigation can be broadly divided into two parts. First, a selection of 14 MVOCs was made based on previous research that characterized the MVOC emissions of Trichoderma atroviride, which is a filamentous fungus widely used as a biocontrol agent. The analysis of gas-phase standards using PTR-ToF-MS allowed for the categorization of these 14 MVOCs into two groups: the first group primarily undergoes nondissociative proton transfer, resulting in the formation of protonated parent ions, while the second group mainly undergoes dissociative proton transfer, leading to the formation of fragment ions. In the second part of this investigation, the emission of MVOCs from samples of T. atroviride was continuously monitored over a period of five days using PTR-ToF-MS. This also included the first quantitative online analysis of 6-amyl-α-pyrone (6-PP), a key MVOC emitted by T. atroviride. The 6-PP emissions of T. atroviride cultures were characterized by a gradual increase over the first two days of cultivation, reaching a plateau-like maximum with volume mixing ratios exceeding 600 ppbv on days three and four. This was followed by a marked decrease, where the 6-PP volume mixing ratios plummeted to below 50 ppbv on day five. This observed sudden decrease in 6-PP emissions coincided with the start of sporulation of the T. atroviride cultures as well as increasing intensities of product ions associated with 1-octen-3-ol and 3-octanone, whereas both these MVOCs were previously associated with sporulation in T. atroviride. The study also presents the observations and discussion of further MVOC emissions from the T. atroviride samples and concludes with a critical assessment of the possible applications and limitations of PTR-ToF-MS for the online monitoring of MVOCs from biological samples in real time.

Metrological generation of SI-traceable gas-phase standards and reference materials for (semi-) volatile organic compounds

EN 16516 sets specifications for the determination of emissions into indoor air from construction products. Reliable, accurate and International System of Unit (SI)-traceable measurement results of the emissions are the key to consumer protection. Such measurement results can be obtained by using metrologically traceable reference materials. Gas-phase standards of volatile organic compounds (VOCs) in air can be prepared by a variety of dynamic methods according to the ISO 6145 series. However, these methods are not always applicable for semi-VOCs (SVOCs) due to their high boiling point and low vapour pressure. Therefore, a novel dynamic gas mixture generation system has been developed. With this system gas-phase standards with trace level VOCs and SVOCs in air can be prepared between 10 nmol mol−1 and 1000 nmol mol−1. The VOCs and SVOCs in this study have normal boiling points ranging from 146 °C to 343 °C. Metrologically traceable reference materials of the gas-phase standard were obtained by sampling of the VOC gas-phase standard into Tenax TA® sorbent material in SilcoNert® coated stainless steel tubes. Accurately known masses between 10 ng and 1000 ng per VOC were sampled. These reference materials were used to validate the dynamic system. Furthermore, the storage and stability periods of the VOCs in the reference materials were determined as these are crucial characteristics to obtain accurate and SI-traceable reference materials. In a round robin test (RRT), the reference materials were used with the aim of demonstrating the feasibility of providing SI-traceable standard reference values for SVOCs for interlaboratory comparison purposes. Based on the results from the validation, the storage and stability studies and the RRT, gas-phase standards and reference materials of VOCs and SVOCs with relative expanded uncertainties between 5% and 12% (k = 2) have been developed. These reference standards can be used as calibrants, reference materials or quality control materials for the analysis of VOC emissions.

Quantification of gas phase hydrogen peroxide and methyl peroxide in ambient air: Using atmospheric pressure chemical ionization mass spectrometry with O2−, and O2−(CO2) reagent ions

Instrumentation and ion chemistry are described for the measurement of hydrogen peroxide (H2O2) and methyl peroxide (CH3OOH) in ambient air by chemical ionization mass spectrometry (CIMS). A CIMS, designed and certified for aircraft deployment, was used in this work. The reagent gas was ultrapure air containing 400ppm CO2. The resultant reagent ions, O2− and O2−(CO2), form cluster ions with CH3OOH and H2O2, respectively, and are monitored at 80m/z [O2−(CH3OOH)] and 110m/z [O2− (CO2)(H2O2)]. The CIMS instrument was periodically calibrated using gas-phase standards generated from aqueous solutions. A Carulite-200® catalyst was used to remove peroxides from ambient air to blank the system to account for variations in the ambient air matrix. H2O2 also forms a stable cluster ion with O2− though its calibration behavior was more complex than that for O2−(CO2) in ambient air. The instrument was deployed on the National Center for Atmospheric Research Gulfstream-V aircraft. Representative measurements from the May-June 2012 Deep Convective Clouds and Chemistry experiment spanning altitudes between 0 and 13km over the south-central midwest and southeastern United States are shown. Laboratory experiments, airborne experiments and theoretical molecular modeling approaches were utilized to identify and select reagent ions and to understand the ion-molecule reactions for the formation of peroxide-ion clusters in the ambient air matrix under tropospheric conditions. The analytical viability of a particular ion-molecule adduct was supported by ab-initio molecular orbital calculations.

Development of methodologies for identification and quantification of hazardous air pollutants from turbine engine emissions

Aircraft turbine engines are a significant source of particulate matter (PM) and gaseous emissions in the vicinity of airports and military installations. Hazardous air pollutants (HAPs) (e.g., formaldehyde, benzene, naphthalene and other compounds) associated with aircraft emissions are an environmental concern both in flight and at ground level. Therefore, effective sampling, identification, and accurate measurement of these trace species are important to assess their environmental impact. This effort evaluates two established ambient air sampling and analysis methods, U.S. Environmental Protection Agency (EPA) Method TO-11A and National Institute for Occupational Safety and Health (NIOSH) Method 1501, for potential use to quantify HAPs from aircraft turbine engines. The techniques were used to perform analysis of the exhaust from a T63 turboshaft engine, and were examined using certified gas standards transferred through the heated sampling systems used for engine exhaust gaseous emissions measurements. Test results show that the EPA Method TO-11A (for aldehydes) and NIOSH Method 1501 (for semivolatile hydrocarbons) were effective techniques for the sampling and analysis of most HAPs of interest. Both methods showed reasonable extraction efficiencies of HAP species from the sorbent tubes, with the exception of acrolein, styrene, and phenol, which were not well quantified. Formaldehyde measurements using dinitrophenylhydrazine (DNPH) tubes (EPA method TO-11A) were accurate for gas-phase standards, and compared favorably to measurements using gas-phase Fourier-transform infrared (FTIR) spectroscopy. In general, these two standard methodologies proved to be suitable techniques for field measurement of turbine engine HAPs within a reasonable (5–10 minutes) sampling period. Details of the tests, the analysis methods, calibration procedures, and results from the gas standards and T63 engine tested using a conventional JP-8 jet fuel are provided.Implications: HAPs from aviation-related sources are important because of their adverse health and environmental impacts in and around airports and flight lines. Simpler, more convenient techniques to measure the important HAPs, especially aldehydes and volatile organic HAPs, are needed to provide information about their occurrence and assist in the development of engines that emit fewer harmful emissions.

Intercomparison of an Aerosol Chemical Speciation Monitor (ACSM) with ambient fine aerosol measurements in downtown Atlanta, Georgia

Abstract. Currently, there are a limited number of field studies that evaluate the long-term performance of the Aerodyne Aerosol Chemical Speciation Monitor (ACSM) against established monitoring networks. In this study, we present seasonal intercomparisons of the ACSM with collocated fine aerosol (PM2.5) measurements at the Southeastern Aerosol Research and Characterization (SEARCH) Jefferson Street (JST) site near downtown Atlanta, GA, during 2011–2012. Intercomparison of two collocated ACSMs resulted in strong correlations (r2 > 0.8) for all chemical species, except chloride (r2 = 0.21) indicating that ACSM instruments are capable of stable and reproducible operation. In general, speciated ACSM mass concentrations correlate well (r2 > 0.7) with the filter-adjusted continuous measurements from JST, although the correlation for nitrate is weaker (r2 = 0.55) in summer. Correlations of the ACSM NR-PM1 (non-refractory particulate matter with aerodynamic diameter less than or equal to 1 μm) plus elemental carbon (EC) with tapered element oscillating microbalance (TEOM) PM2.5 and Federal Reference Method (FRM) PM1 mass are strong with r2 > 0.7 and r2 > 0.8, respectively. Discrepancies might be attributed to evaporative losses of semi-volatile species from the filter measurements used to adjust the collocated continuous measurements. This suggests that adjusting the ambient aerosol continuous measurements with results from filter analysis introduced additional bias to the measurements. We also recommend to calibrate the ambient aerosol monitoring instruments using aerosol standards rather than gas-phase standards. The fitting approach for ACSM relative ionization for sulfate was shown to improve the comparisons between ACSM and collocated measurements in the absence of calibrated values, suggesting the importance of adding sulfate calibration into the ACSM calibration routine.

Effect of standard phase differences between gas and liquid and the resulting experimental bias in the analysis of gaseous volatile organic compounds

Liquid- or gas-phase standards can be used for the analysis of VOCs in air. Once the accuracy is secured in the standard preparation stage, the use of gas-phase standard should be more reliable with the least matrix effect. However, it is not difficult to find that the liquid-phase standard is used more preferably in many laboratories for several reasons (e.g., low expense, easy handling, etc.). As such, one needs to accurately evaluate any possible bias stemming from the use of different standard phases. To this end, standards for 8 VOCs consisting of 4 aromatic compounds (benzene (B), toluene (T), styrene (S) and p-xylene (p-X)) and 4 others (methyl ethyl ketone (MEK), methyl isobutyl ketone (MIBK), butyl acetate (BuAc), and isobutyl alcohol (i-BuAl)) were prepared in both liquid and gas phases. Each standard was analyzed by the initial collection on the adsorption tube and by the combined application of thermal-desorption–gas chromatography–mass spectrometry (TD/GC/MS). The results indicated that experimental bias between the two phases, if expressed in terms of percent difference (PD), was very low in many target VOCs (B (1.09%), T (2.41%), p-X (3.64%), MEK (6.76%), and MIBK (0.17%)), while it was not in some targets (e.g., >10%: e.g., S, i-BuAl, and BuAc). In an ancillary experiment, biases were evaluated further by (1) calibrating gaseous samples against liquid phase standard and via (2) comparison between two different types of gas phase standards. In conclusion, treatment of different standards (e.g., between the same or different phases) will inevitably induce biases in most VOCs, although certain volatiles (e.g., benzene, MIBK, etc.) are virtually unaffected by such variables in a practical sense.

Field inter-comparison of eleven atmospheric ammonia measurement techniques

Abstract. Eleven instruments for the measurement of ambient concentrations of atmospheric ammonia gas (NH3), based on eight different measurement methods were inter-compared above an intensively managed agricultural field in late summer 2008 in Southern Scotland. To test the instruments over a wide range of concentrations, the field was fertilised with urea midway through the experiment, leading to an increase in the average concentration from 10 to 100 ppbv. The instruments deployed included three wet-chemistry systems, one with offline analysis (annular rotating batch denuder, RBD) and two with online-analysis (Annular Denuder sampling with online Analysis, AMANDA; AiRRmonia), two Quantum Cascade Laser Absorption Spectrometers (a large-cell dual system; DUAL-QCLAS, and a compact system; c-QCLAS), two photo-acoustic spectrometers (WaSul-Flux; Nitrolux-100), a Cavity Ring Down Spectrosmeter (CRDS), a Chemical Ionisation Mass Spectrometer (CIMS), an ion mobility spectrometer (IMS) and an Open-Path Fourier Transform Infra-Red (OP-FTIR) Spectrometer. The instruments were compared with each other and with the average concentration of all instruments. An overall good agreement of hourly average concentrations between the instruments (R2>0.84), was observed for NH3 concentrations at the field of up to 120 ppbv with the slopes against the average ranging from 0.67 (DUAL-QCLAS) to 1.13 (AiRRmonia) with intercepts of −0.74 ppbv (RBD) to +2.69 ppbv (CIMS). More variability was found for performance for lower concentrations (<10 ppbv). Here the main factors affecting measurement precision are (a) the inlet design, (b) the state of inlet filters (where applicable), and (c) the quality of gas-phase standards (where applicable). By reference to the fast (1 Hz) instruments deployed during the study, it was possible to characterize the response times of the slower instruments.

Effects of injection volume change on gas chromatographic sensitivity determined with two contrasting calibration approaches for volatile organic compounds

In this study, the effects of injection volume change on gas chromatographic detection properties have been evaluated using gas-phase standards containing three aromatic volatile organic compounds (VOC): benzene, toluene, and xylene (commonly called BTX). To examine such effects on GC sensitivity, a series of calibration data sets were obtained using standards of three concentration values (3, 6, and 10 ppm) at each of five selected injection volumes (20 to 1000 microL). The results were initially examined in terms of the fixed standard volume (FSV) approach to allow the direct comparison of calibration patterns between different injection volumes. Identical data sets were then re-organized so that the calibration data could also be compared across variable injection volumes for a given standard concentration (at all three concentrations), i.e. by the fixed standard concentration (FSC) approach. The results of our comparative analysis between the FSV and the FSC approaches indicate that the calibration patterns of VOC are highly sensitive to changes in injection volume or injection-related conditions. It is thus suggested that the former approach is more reasonable for reducing uncertainties associated with the GC-based quantification of atmospheric pollutants.