scholarly journals UiO-66 Selective Enrichment Integrated with Thermal Desorption GC-MS for Detection of Benzene Homologues in Ambient Air

2021 ◽  
Vol 2021 ◽  
pp. 1-9
Author(s):  
Xing-Tao Lin ◽  
Ge Sun ◽  
Jing-Qiang Zhao ◽  
Ling-Li Tang ◽  
Sheng-Hua Li ◽  
...  
Keyword(s):  
Thermal Desorption ◽  
Indoor Air ◽  
Detection Limits ◽  
Ambient Air ◽  
Selective Enrichment ◽  
Relative Standard ◽  
Sampling Volume ◽  
Benzene Homologues ◽  
Benzene Toluene ◽  
Series Of Experiments

In this study, UiO-66 was selected as sorbent media packed in the tube to selectively enrich trace levels of benzene homologues such as benzene, toluene, and xylene (BTX) in ambient air prior to thermal desorption (TD)-GC-MS determination. A series of experiments were conducted to obtain the optimal TD conditions. The results indicated that the optimal TD parameters were as follows: desorption temperature of 180°C, desorption flow rate of 50 mL min−1, and desorption time of 30 min. Furthermore, the method based on UiO-66 enrichment integrated with TD-GC-MS for trace levels of BTX was successfully developed. It exhibited a good linearity (R2 > 0.99) in the range of 50–1000 ng, except for p, m-xylene in the range of 100–2000 ng, and achieved the recovery of 69.4–101.3%, and the relative standard deviation of 3.8–6.4%. The detection limits of BTX were 1.6–4.0 ng; according to 10 L of sampling volume, the method detection limits would be in the range of 0.16–0.40 µg m−3. Additionally, the method was successfully applied to determine BTX in indoor air and showed good selectivity and sensitivity. In summary, the findings in this work revealed that UiO-66 was an attractive adsorbent for selective enrichment trace levels of BTX compounds in ambient air, which was favorable for the subsequent detection by TD-GC-MS.

Thermal Desorption Solid-Phase Microextraction Inlet for Differential Mobility Spectrometry

2005 ◽  
Vol 59 (6) ◽  
pp. 754-762 ◽  
Author(s):  
Matthew R. Rainsberg ◽  
Peter de B. Harrington
Keyword(s):  
Environmental Monitoring ◽  
Thermal Desorption ◽  
Ion Mobility ◽  
Solid Phase Microextraction ◽  
Solid Phase ◽  
Detection Limits ◽  
Differential Mobility Spectrometry ◽  
Differential Mobility ◽  
Benzene Toluene ◽  
Detection Capabilities

A splitless thermal desorber unit that interfaces a differential mobility spectrometry (DMS) sensor has been devised. This device was characterized by the detection of benzene, toluene, and xylene (BTX) in water. The detection of BTX in water is important for environmental monitoring, and ion mobility measurements are traditionally difficult for hydrocarbons in water because water competes for charge and quenches the hydrocarbon signals. This paper reports the use of a DMS with a photoionization source that is directly coupled to a solid-phase microextraction (SPME) desorber. The separation and detection capabilities of the DMS were demonstrated using BTX components. Detection limits for benzene, toluene, and m-xylene were 75, 50, and 5 μg mL−1, respectively.

scholarly journals Field Study of Metal Oxide Semiconductor Gas Sensors in Temperature Cycled Operation for Selective VOC Monitoring in Indoor Air

Atmosphere ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 647
Author(s):  
Tobias Baur ◽  
Johannes Amann ◽  
Caroline Schultealbert ◽  
Andreas Schütze
Keyword(s):  
Air Quality ◽  
Metal Oxide ◽  
Gas Sensor ◽  
Gas Sensors ◽  
Indoor Air ◽  
Ambient Air ◽  
Quantitative Agreement ◽  
Metal Oxide Semiconductor ◽  
Oxide Semiconductor ◽  
High Temporal Resolution

More and more metal oxide semiconductor (MOS) gas sensors with digital interfaces are entering the market for indoor air quality (IAQ) monitoring. These sensors are intended to measure volatile organic compounds (VOCs) in indoor air, an important air quality factor. However, their standard operating mode often does not make full use of their true capabilities. More sophisticated operation modes, extensive calibration and advanced data evaluation can significantly improve VOC measurements and, furthermore, achieve selective measurements of single gases or at least types of VOCs. This study provides an overview of the potential and limits of MOS gas sensors for IAQ monitoring using temperature cycled operation (TCO), calibration with randomized exposure and data-based models trained with advanced machine learning. After lab calibration, a commercial digital gas sensor with four different gas-sensitive layers was tested in the field over several weeks. In addition to monitoring normal ambient air, release tests were performed with compounds that were included in the lab calibration, but also with additional VOCs. The tests were accompanied by different analytical systems (GC-MS with Tenax sampling, mobile GC-PID and GC-RCP). The results show quantitative agreement between analytical systems and the MOS gas sensor system. The study shows that MOS sensors are highly suitable for determining the overall VOC concentrations with high temporal resolution and, with some restrictions, also for selective measurements of individual components.

scholarly journals Rapid Determination of Ethylene Oxide and 75 VOCs in Ambient Air with Canister Sampling and Associated Growth Issues

Separations ◽  
2021 ◽  
Vol 8 (3) ◽  
pp. 35
Author(s):  
Jason Hoisington ◽  
Jason S. Herrington
Keyword(s):  
Ethylene Oxide ◽  
Rapid Determination ◽  
Complex Mixture ◽  
Ambient Air ◽  
Gas Chromatography Mass Spectrometry ◽  
Average Accuracy ◽  
Relative Standard ◽  
Wide Range ◽  
Us Epa

A canister-based sampling method along with preconcentrator-Gas chromatography-Mass Spectrometry (GC-MS) analysis was applied to ethylene oxide (EtO or EO) and 75 other volatile organic compounds (VOCs) in ambient air. Ambient air can contain a large variety of VOCs, and thorough analysis requires non-discriminatory sampling and a chromatographic method capable of resolving a complex mixture. Canister collection of whole air samples allows for the collection of a wide range of volatile compounds, while the simultaneous analysis of ethylene oxide and other VOCs allows for faster throughput than separate methods. The method presented is based on US EPA Method TO-15A and allows for the detection of EtO from 18 to 2500 pptv. The method has an average accuracy of 104% and precision of 13% relative standard deviation (RSD), with an instrument run time of 32 min. In addition, a link between canister cleanliness and ethylene oxide growth is observed, and potential mechanisms and cleaning strategies are addressed.

scholarly journals Determination of Glycol Ethers in Ambient Air by Adsorption Sampling and Thermal Desorption with GC/MS Analysis: Performance Evaluation and Field Application

2012 ◽  
Vol 9 (2) ◽  
pp. 970-979
Author(s):  
Young-Kyo Seo ◽  
Sung-Ok Baek
Keyword(s):  
Thermal Desorption ◽  
Analytical Method ◽  
Ambient Air ◽  
Industrial Area ◽  
Field Application ◽  
Ambient Atmosphere ◽  
Glycol Ethers ◽  
Ms Analysis ◽  
Sampling Campaign

Some of glycol ethers, such as 2-methoxyethanol (2-ME) and 2-ethoxyethanol (2-EE) are known to be toxic and classified as hazardous air pollutants in USA, Japan and Germany. In Korea, however, there has been no study conducted so far for these compounds in ambient air. In addition, no clear methodologies for the measurement of glycol ethers have been yet established. We carried out this study to evaluate a sampling and analytical method for the determination of glycol ethers, in ambient air samples collected in specific industrial areas of South Korea. To measure glycol ethers, adsorption sampling and thermal desorption with GC/MS analysis were used in this study. The analytical method showed good repeatability, linearity and sensitivity. The lower detection limits were estimated to be approximately 0.3∼0.5 ppb. Based on storage tests, it was suggested that samples should be analyzed within two weeks. It was also demonstrated that this method can be used for the simultaneous measurement of glycol ethers and other aromatic VOCs such as benzene, toluene, and xylenes. Field sampling campaign was carried out at 2 sites, located in a large industrial area, from October 2006 to June 2007, and a total of 480 samples were collected seasonally. Among them, 2-ME was not detected from any samples, while 2-EE and 2-Ethyloxyethylacetate (2-EEA) were found in 7 and 70 samples, respectively. The measured concentrations of 2-EE and 2-EEA for samples were ranged from 0.7-2.5 ppb and from 0.5-10.5 ppb, respectively. To our knowledge, this is the first measurement report for glycol ethers in the ambient atmosphere not only in Korea but also the rest of the world.

Measurements of metabolic rate in rats: a comparison of techniques

1988 ◽  
Vol 65 (2) ◽  
pp. 964-970 ◽  
Author(s):  
T. I. Musch ◽  
A. Bruno ◽  
G. E. Bradford ◽  
A. Vayonis ◽  
R. L. Moore
Keyword(s):  
Metabolic Rate ◽  
Maximal Exercise ◽  
Ambient Air ◽  
Open Circuit ◽  
Submaximal Exercise ◽  
Co2 Production ◽  
Arterial Blood ◽  
In Series ◽  
Series Of Experiments ◽  
Four Levels

Two different open-circuit techniques of measuring metabolic rate were examined in rats at rest and during exercise. With one technique ambient air was drawn through a tightly fitting mask that was secured to the rat's head, whereas with the other technique the rat was placed into and ambient air was drawn through a Plexiglas box. Two series of experiments were performed. In series I, two groups were studied that consisted of rats that had received myocardial infarctions produced by coronary arterial ligations and rats that had received sham operations. In this series of experiments O2 uptake (VO2) and CO2 production (VCO2) were measured at rest, during four levels of submaximal exercise, and during maximal treadmill exercise in the same group of rats by use of both techniques in random order. VO2, VCO2, and the calculated respiratory exchange ratio (R) were similar at rest, during the highest level of submaximal exercise (20% grade, 37 m/min), and during maximal exercise; however, VO2 and VCO2 were significantly lower with the metabolic box technique compared with the mask technique during the three lowest work loads (5% grade, 19 m/min; 10% grade, 24 m/min; and 15% grade, 31 m/min). These differences appeared to be associated with a change in gait produced when the mask was worn. In series II, the arterial blood gas and acid-base responses to both submaximal and maximal exercise were measured using both techniques in a group of instrumented rats that had a catheter placed into the right carotid artery.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals Amines in boreal forest air at SMEAR II station in Finland

2018 ◽  
Vol 18 (9) ◽  
pp. 6367-6380 ◽  
Author(s):  
Marja Hemmilä ◽  
Heidi Hellén ◽  
Aki Virkkula ◽  
Ulla Makkonen ◽  
Arnaud P. Praplan ◽  
...  
Keyword(s):  
Boreal Forest ◽  
Gas Phase ◽  
Particle Number ◽  
Detection Limits ◽  
Ambient Air ◽  
Monthly Means ◽  
Ammonium Ions ◽  
Quadrupole Mass ◽  
Concentration Data ◽  
Diurnal Variability

Abstract. We measured amines in boreal forest air in Finland both in gas and particle phases with 1 h time resolution using an online ion chromatograph (instrument for Measuring AeRosols and Gases in Ambient Air – MARGA) connected to an electrospray ionization quadrupole mass spectrometer (MS). The developed MARGA-MS method was able to separate and detect seven different amines: monomethylamine (MMA), dimethylamine (DMA), trimethylamine (TMA), ethylamine (EA), diethylamine (DEA), propylamine (PA), and butylamine (BA). The detection limits of the method for amines were low (0.2–3.1 ng m−3), the accuracy of IC-MS analysis was 11–37 %, and the precision 10–15 %. The proper measurements in the boreal forest covered about 8 weeks between March and December 2015. The amines were found to be an inhomogeneous group of compounds, showing different seasonal and diurnal variability. Total MMA (MMA(tot)) peaked together with the sum of ammonia and ammonium ions already in March. In March, monthly means for MMA were < 2.4 and 6.8 ± 9.1 ng m−3 in gas and aerosol phases, respectively, and for NH3 and NH4+ these were 52 ± 16 and 425 ± 371 ng m−3, respectively. Monthly medians in March for MMA(tot), NH3, and NH4+ were < 2.4, 19 and 90 ng m−3, respectively. DMA(tot) and TMA(tot) had summer maxima indicating biogenic sources. We observed diurnal variation for DMA(tot) but not for TMA(tot). The highest concentrations of these compounds were measured in July. Then, monthly means for DMA were < 3.1 and 8.4 ± 3.1 ng m−3 in gas and aerosol phases, respectively, and for TMA these were 0.4 ± 0.1 and 1.8 ± 0.5 ng m−3. Monthly medians in July for DMA were below the detection limit (DL) and 4.9 ng m−3 in gas and aerosol phases, respectively, and for TMA these were 0.4 and 1.4 ng m−3. When relative humidity of air was > 90 %, gas-phase DMA correlated well with 1.1–2 nm particle number concentration (R2=0.63) suggesting that it participates in atmospheric clustering. EA concentrations were low all the time. Its July means were < 0.36 and 0.4 ± 0.4 ng m−3 in gas and aerosol phases, respectively, but individual concentration data correlated well with monoterpene concentrations in July. Monthly means of PA and BA were below detection limits at all times.

scholarly journals Identification and quantification of organic pollutants in the air of the city of Astana using solid phase microextraction

2017 ◽  
pp. 14-17
Author(s):  
Dina Orazbayeva ◽  
Ulzhalgas Karatayeva ◽  
Kulzhan Beysembayeva ◽  
Kulyash Meyramkulova
Keyword(s):  
Polycyclic Aromatic Hydrocarbons ◽  
Aromatic Hydrocarbons ◽  
Solid Phase Microextraction ◽  
Solid Phase ◽  
Ambient Air ◽  
Average Concentration ◽  
Polycyclic Aromatic ◽  
Benzene Toluene ◽  
The City

Solid-phase microextraction in combination with gas chromatography and mass-spectrometry (GC-MS) was used for determination of benzene, toluene, ethylbenzene and o-xylene (BTEX), polycyclic aromatic hydrocarbons (PAH), and for identification of volatile organic compounds (VOCs) in ambient air of the city of Astana, Kazakhstan. The screening of the samples showed the presence of mono- and polycyclic aromatic hydrocarbons, alkanes, alkenes, phenols, and benzaldehydes. The concentrations of naphthalene were 5-7 times higher than the permissible value, it was detected in all studied air samples. Average concentration of naphthalene was 18.4 μg/m3, acenaphthylene – 0.54 μg/m3, acenaphthene – 1.63 μg/m3, fluorene – 0.79 μg/m3, anthracene – 3.27 μg/m3, phenanthrene – 0.22 μg/m3, fluorantene – 0.74 μg/m3, pyrene – 0.73 μg/m3. Average concentrations of BTEX in the studied samples were 31.1, 84.9, 10.8 and 11.6 μg/m3, respectively. Based on the statistical analysis of the concentrations of BTEX and PAH, the main source of city air pollution with them was assumed to be vehicle emissions.

scholarly journals Removal of contaminants in indoor air by using green plant treated with titanium dioxide nanoparticles

2019 ◽  
Author(s):  
Khaled Fikry salama ◽  
Mubashir Zafar Zafar
Keyword(s):  
Air Pollution ◽  
Titanium Dioxide ◽  
Indoor Air ◽  
Indoor Air Pollution ◽  
Titanium Dioxide Nanoparticles ◽  
Plant Root ◽  
Ambient Air ◽  
Green Plant ◽  
Growth Media ◽  
Novel Approach

Abstract Background: Indoor air pollution is important environmental health problem. Nanotechnology is one of the most important methods to reduce the air pollution. The aim of this study to determine the effectiveness of nanotechnology for removal of toxic air indoor pollution by using Saudi myrtle plants treated with titanium dioxide. Methods: Experiments were conducted in the two academic departments of labs at public sector universities. Aplying titanium dioxide-containing growth media to at least one of a Myrtus communis plant root, stem, and leaf. Growing the plant in the growth media, a gel growth media, or both; exposing the plant to contaminant-containing air Results: It is found that the levels of formaldehyde, Volatile organic compounds and other pollutants were significantly reduced the concentration from 10% to 98% in air. The duration of the intervention from 4 hours to 8 hours, Air containing the concentration of NO2 SO2, formaldehyde, TVOCs and CO reduced from range of 0.3 ppm- 0.4ppm to range of 0.1ppm -0.3 ppm after exposure of Myrtus plant to ambient air and duration of the exposure is 4 hours to 8 hours. Conclusion: Application of Tio2 in green plant specially Mytrus Communis is a novel approach for reduction of concentrations of harmful gaseous toxic and carcinogenic air pollutants in indoor environment.

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