Nonpolar Volatile Organic Compounds Research Articles

Synthesis of 4-vinylpyridine–divinylbenzene copolymer adsorbents for microwave-assisted desorption of benzene

Reports on the development of polymer adsorbents for microwave-assisted desorption of nonpolar volatile organic compounds (VOCs) are rare. In this study, we synthesized macroporous polymeric adsorbents with hydrophilic methyl pyridinium units for microwave-assisted desorption of nonpolar VOCs. The benzene adsorption and desorption properties of the adsorbents were investigated under both dry and humid conditions. Under humid conditions, as the content of the hydrophilic methyl pyridinium units in the adsorbents increased from 0 to 20%, the adsorption capacity of benzene decreased from about 21 to 7mg/g, while the desorption efficiency of benzene increased significantly from 48 to 87%. The maximum concentration of desorbate also increased significantly as the content of the hydrophilic units was increased under humid conditions. We attributed the enhanced desorption efficiency mainly to more adsorbed moisture, which indirectly allowed heating of the polymer adsorbents to higher temperatures upon irradiation with 600W microwaves.

Single-walled carbon nanotube-based biosensors for the detection of volatile organic compounds of lung cancer

Detection of volatile organic compounds (VOCs) in human breath to diagnose lung cancer is becoming an important method for widespread screening due to its convenient, rapid and low cost advantages. In this paper, experimental evidence for the detection of both polar and nonpolar VOCs molecules by organic materials functionalized single-walled carbon nanotubes (SWNTs) was investigated. To develop a high-selectivity SWNTs biosensor, nonpolymeric organic materials, tricosane (C 23H 48) and pentadecane (C 15H 32) were coated on the single-walled carbon nanotubes (SWNTs) and the prepared device was exposed to representative VOCs polar molecule 1,2,4-trimethybenzene (TMB) and nonpolar molecule decane separately. The results show that the resistance changes of SWNTs biosensor increased to 2.3% for decane and 7.2% for TMB after being functionalized by C 23H 48; meanwhile, the variation of 3.3% for decane and 5.1% for TMB was observed by C 15H 32-functionalized SWNTs. The results present that C 23H 48-functionalized SWNTs show pronounced sensitivity toward polar VOCs molecules, which can donate electrons to the SWNTs after being absorbed. This research is a further step toward the development of a simple and noninvasive diagnostic tool for the widespread screening of lung cancer via breath analysis.

Nanoarray of Polycyclic Aromatic Hydrocarbons and Carbon Nanotubes for Accurate and Predictive Detection in Real-World Environmental Humidity

In the present work, we introduce a cross-reactive array of synthetically designed polycyclic aromatic hydrocarbons (PAH) and single-walled carbon nanotube (SWCNT) bilayers and demonstrate the huge potential of the array in discriminating between polar and nonpolar volatile organic compounds (VOCs), as well as between the different VOCs from each subgroup. Using appropriate combinations of PAH/SWCNT sensors, we demonstrate that high sensitivity and accuracy values can be obtained for discriminating polar and nonpolar VOCs in samples with variable humidity levels (5-80% RH). The same array of sensors exhibited self-learning capabilities that facilitated exchanging information about environmental properties under observation. The results presented here could lead to the development of a cost-effective, lightweight, low-power, and non-invasive tool for a widespread detection of VOCs in real-world environmental, security, food, health, and other applications.

VOC amounts in ambient areas of a high-technology science park in Taiwan: their reciprocal correlations and impact on inhabitants

This study presents bihourly, seasonal, and yearly concentration changes in volatile organic compounds (VOCs) in the inlet and effluent water of the wastewater treatment plant (WWTP) of a high-technology science park (HTIP) in Taiwan, with the VOC amounts at different sites correlated geologically. This research adopted a combination of two systems, solid-phase microextraction with a gas chromatography/flame ionization detector and an assembly of purge and trap coupled with gas chromatography/mass spectrometry, to monitor polar and nonpolar VOCs in wastewater. This paper investigated the total VOCs, acetone, isopropyl alcohol (IPA), and dimethylsulfide (DMS) concentrations in real water samples collected in the ambient area of the HTIP. The major contents of VOCs measured in the effluent of the WWTP in the HTIP and the surrounding river region were DMS (14-176 ppb), acetone (5-95 ppb), and IPA (15-316 ppb). In comparison with the total VOCs in the inlet wastewater of the WWTP, no corresponding relationship for total VOC concentration in the wastewater was observed between the inlet water and effluent water of the WWTP. The peak VOC concentrations appeared in the third season, and the correlation of different VOC amounts reflects the production situation of the factories. In addition, VOC concentrations at different sites indicate that the Ke-Ya River is seemingly an effective channel for transporting wastewater to its final destination. The data are good indications for the management of environmental pollution near the HTIP.

Enhanced Sensing of Nonpolar Volatile Organic Compounds by Silicon Nanowire Field Effect Transistors

Silicon nanowire field effect transistors (Si NW FETs) are emerging as powerful sensors for direct detection of biological and chemical species. However, the low sensitivity of the Si NW FET sensors toward nonpolar volatile organic compounds (VOCs) is problematic for many applications. In this study, we show that modifying Si NW FETs with a silane monolayer having a low fraction of Si-O-Si bonds between the adjacent molecules greatly enhances the sensitivity toward nonpolar VOCs. This can be explained in terms of an indirect sensor-VOC interaction, whereby the nonpolar VOC molecules induce conformational changes in the organic monolayer, affecting (i) the dielectric constant and/or effective dipole moment of the organic monolayer and/or (ii) the density of charged surface states at the SiO(2)/monolayer interface. In contrast, polar VOCs are sensed directly via VOC-induced changes in the Si NW charge carriers, most probably due to electrostatic interaction between the Si NW and polar VOCs. A semiempirical model for the VOC-induced conductivity changes in the Si NW FETs is presented and discussed.

Synthesis of Hydroxylated Macroporous Polymer Beads for Microwave-Assisted Desorption of Nonpolar Volatile Organic Compounds

Opperman and Brown reported a microwave-assisted volatile organic compounds (VOCs) recovery system with polymer bead adsorbents, with emphasis on significant advantages over the conventional granulated activated carbon-based systems in terms of cost and energy efficiency, but details on their experimental results were not included.

Carbon Nanotube/Hexa‐peri‐hexabenzocoronene Bilayers for Discrimination Between Nonpolar Volatile Organic Compounds of Cancer and Humid Atmospheres

Cancer detection: The development of a cost-effective, portable and non-invasive diagnostic tool for detecting cancer from exhaled breath requires sensors that discriminate well between polar and nonpolar volatile organic compounds in highly humid atmospheres. Here we show that a chemiresistive bilayer comprised of a dense cap layer of discotic hexa-dodecyl-hexa-peri-hexabenzocoronene derivatives (hereby, HBC-C12) and a random network of carbon nanotubes (RN-CNT) as underlayer layer could fulfill these requirements.

Spongelike Structures of Hexa-peri-hexabenzocoronene Derivatives Enhance the Sensitivity of Chemiresistive Carbon Nanotubes to Nonpolar Volatile Organic Compounds of Cancer

Cancer is a leading health hazard, and lung cancer is its most common form. Breath testing is a fast, noninvasive diagnostic method which links specific volatile organic compounds (VOCs) in exhaled breath to medical conditions. Arrays of sensors based on carbon nanotubes (CNTs) could in principle detect cancer by differentiating between the VOCs found in the breath of healthy and sick persons, but the notoriously low sensitivity of CNT sensors to nonpolar VOCs limits their accuracy. In this study, we have achieved a marked improvement of the sensitivity and selectivity of random networks (RNs) of CNT chemiresistors to nonpolar VOCs by functionalizing them with self-assembled, spongelike structures of discotic hexa-peri-hexabenzocoronene (HBC) derivatives. We observed swelling of the organic film by monitoring the changes of organic film thickness during exposure and propose that the expansion of the spongelike organic overlayer creates scattering centers in the underlying RN-CNTs by physically distancing the CNTs at their intersections. The results presented here could lead to the development of robust sensors for nonpolar VOCs of cancer breath, which have hitherto been difficult to trace.

Simultaneous quantification of polar and non-polar volatile organic compounds in water samples by direct aqueous injection-gas chromatography/mass spectrometry

A direct aqueous injection-gas chromatography/mass spectrometry (DAI-GC/MS) method for trace analysis of 24 volatile organic compounds (VOCs) in water samples is presented. The method allows for the simultaneous quantification of benzene, toluene, ethyl benzene, and xylenes (BTEX), methyl tert-butyl ether (MTBE), tert-butyl alcohol (TBA), as well as a variety of chlorinated methanes, ethanes, propane, enthenes and benzenes. Applying a liquid film polyethylene glycol or a porous layer open tubular (PLOT) divinylbenzene GC capillary column to separate the water from the VOCs, volumes of 1–10 μL aqueous sample are directly injected into the GC. No enrichment or pretreatment steps are required and sample volumes as low as 100 μL are sufficient for accurate quantification. Method detection limits determined in natural groundwater samples were between 0.07 and 2.8 μg/L and instrument detection limits of <5 pg were achieved for 21 out of the 24 evaluated VOCs. DAI-GC/MS offers both good accuracy and precision (relative standard deviations ≤10%). The versatility of our method is demonstrated for contaminant quantification in drinking water disinfection (advanced oxidation of MTBE) and for VOC concentration measurements in a polluted aquifer. The wide range of detectable compounds and the lack of labor-intensive sample preparation illustrate that the DAI method is robust and easily applicable for the quantification of important organic groundwater contaminants.

DBR-structured smart particles for sensing applications

The micro-particles containing a periodic nanostructure have been generated from the distributed Bragg reflector (DBR) porous silicon (PSi) by ultrasono-method and exhibit a sharp photonic band in the optical reflectivity spectrum. These particles are optically encoded with Bragg-structured photonic band and their sizes are about 500nm to few micron. Reflection spectrum of smart particles indicates that the full-width at half-maximum (FWHM) is of 18nm and much narrower than that of fluorescent organic molecules or quantum dot. The detection of volatile organic compounds (VOCs) using these particles has been achieved. The surface of these particles has been chemically modified to have different physical surface properties. When the vapor of VOCs condenses in the nanopores, the refractive indices of entire particle increase. This results in a red shift in the photonic peak depending on the surface property. Particles modified with dodecyl functionality exhibit the most red-shifted photonic feature for nonpolar VOCs (ca. hexane, 25nm; methanol, 12nm), however particles modified with hydroxyl group display vice versa (ca. hexane, 15nm; methanol, 24nm).

Determining Chemical Activity of (Semi)volatile Compounds by Headspace Solid-Phase Microextraction

This research introduces a new analytical methodology for measuring chemical activity of nonpolar (semi)volatile organic compounds in different sample matrices using automated solid-phase microextraction (SPME). The chemical activity of an analyte is known to determine its equilibrium concentration in the SPME fiber coating. On this basis, SPME was utilized for the analytical determination of chemical activity, fugacity, and freely dissolved concentration using these steps: (1) a sample is brought into a vial, (2) the SPME fiber is introduced into the headspace and equilibrated with the sample, (3) the SPME fiber is injected into the GC for thermal desorption and analysis, and (4) the method is calibrated by SPME above partitioning standards in methanol. Model substances were BTEX, naphthalene, and alkanes, which were measured in a variety of sample types: liquid polydimethylsiloxane (PDMS), wood, soil, and nonaqueous phase liquid (NAPL). Variable sample types (i.e., matrices) had no influence on sampling kinetics because diffusion through the headspace was rate limiting for the overall sampling process. Sampling time was 30 min, and relative standard deviations were generally below 5% for homogeneous solutions and somewhat higher for soil and NAPL. This type of activity measurement is fast, reliable, almost solvent free, and applicable for mixed-media sampling.

Comparison of in-tube sorptive extraction techniques for non-polar volatile organic compounds by gas chromatography with mass spectrometric detection

A commercial in-tube sorptive extraction device, known as solid-phase dynamic extraction (SPDE), has been evaluated for the extraction of non-polar volatile aromatic analytes from aqueous solutions in both headspace and liquid injection modes. An automated sampler is used with a gas-tight 2.5 ml syringe equipped with a special needle that is coated on the inside with a non-polar extraction phase. After absorption onto the phase, the analytes were thermally desorbed directly into a GC–MS system. The technique was evaluated for the determination of furan, benzene and toluene. The sensitivity for toluene was greatly improved on using SPDE compared to static headspace. A slight increase in sensitivity was observed for benzene but none for determination of furan. Estimated limits of detection ranged from 0.2 to 2 μg/l.

Determination of complex mixtures of volatile organic compounds in ambient air: canister methodology

Canister methodology is applicable to 150 polar and nonpolar VOCs found in ambient air from parts-per-billion by volume (ppbv) to parts-per-million (ppmv) levels, and has been validated at parts-per-trillion (pptv) levels for a subset of these analytes. This article is a detailed review of techniques related to the collection of volatile organic compounds (VOCs) in evacuated Summa and fused-silica-lined canisters, and their analysis by gas chromatography/mass spectrometry (GC/MS). Emphasis is placed on canister cleaning, VOC stability in canisters, sample dilution, water management, and VOC cryogenic and sorbent preconcentration methods. A wide range of VOC preconcentration and water management methods are identified from the literature, and their relative merits and disadvantages are discussed. Examples of difficulties that commonly arise when processing canister samples are illustrated, and solutions to these problems are provided.

Detection of volatile organic compounds by temperature-programmed desorption combined with mass spectrometry and Fourier transform infrared spectroscopy

A temperature-programmed desorption (TPD) device connected to a mass spectrometer was used to detect volatile organic compounds from air samples. The main aim was to develop an analytical method, by which both non-polar and polar organic components can be detected in the same run. In TPD, the adsorbed compounds are desorbed from the resin more slowly than in the conventional trapping techniques, such as purge-and-trap technique, in which the resin is flash-heated and the compounds are desorbed at the same time to a cryogenic trap or an analytical column. In TPD, the adsorbent resin acts also as an analytical column. In this way it is possible to obtain more rapid analysis, and also a more simple instrumentation, which can be used on-line and on-site. In this work, a new version of TPD device, which uses a resistor for heating and a Peltier element for rapid cooling, was designed and constructed. Various adsorbent resins were tested for their adsorption and desorption properties of both polar and non-polar compounds. When using a mixture of adsorbent resins, Tenax TA and HayeSep D, it was possible to analyze both polar, low-molecular weight compounds, such as methanol and ethanol, and non-polar volatile organic compounds, such as benzene and toluene, in the same run within 15 min including sampling. The same TPD principle was also tested using a Fourier transform infrared spectrometer as an analytical instrument, and the results showed that it was possible to obtain a separation of similar compounds, such as hexane and heptane, and still retaining the same sensitivity as the original on-line FTIR instrument.

Method for Analysis of Polar Volatile Trace Components in Aqueous Samples by Gas Chromatography

A new method has been developed for direct analysis of volatile polar trace compounds in aqueous samples by gas chromatography. Water samples are injected onto a short packed precolumn containing anhydrous lithium chloride. A capillary column is coupled in series with the prefractionation column for final separation of the analytes. The enrichment principle of the salt precolumn is reverse to the principles employed in conventional methods such as SPE or SPME in which a sorbent or adsorbent is utilized to trap or concentrate the analytes. Such methods are not efficient for highly polar compounds. In the LiCl precolumn concept, the water matrix is strongly retained on the hygroscopic salt, whereas polar as well as nonpolar volatile organic compounds show very low retention and are eluted ahead of the water. After transfer of the analytes to the capillary column, the retained bulk water is removed by backflushing the precolumn at elevated temperature. For direct injections of 120 microL of aqueous samples, the combined time for injection and preseparation is only 3.5 min. With this procedure, direct repetitive automated analyses of highly volatile polar compounds such as methanol or tetrahydrofuran can be performed, and a limit of quantification in the low parts-per-billion region utilizing a flame ionization detector is demonstrated.

Adsorption–Desorption Rate of Nonpolar Volatile Organic Compounds onto Activated Carbon Exemplified by C6H6 and CCl4

This investigation was to evaluate the performance of a thermodynamic model using nonlinear driving force in conjunction with the Langmuir model exemplified by the adsorption of benzene and carbon tetrachloride onto activated carbon in mono- and binary-adsorbate systems. Results show that model-fitted adsorption and desorption rate constants could well predict the adsorption isotherms and breakthrough curves under various conditions. This numerical model can provide adsorption and desorption rate constants. The kinetic parameters are of the same order of magnitude as reported in several studies. Under high reaction temperatures, both the adsorption and desorption rate constants increased while equilibrium constants decreased. A dimensionless valuable C0/K can be used to describe the relationship between adsorbate and adsorbent, and predict the service cycle during the adsorption process. For adsorption in binary mixtures, a high inlet concentration or a low temperature, the weak adsorbate, C6H6, will have...

The synthesis of 3-octadecyl- and 3-docosylpyrrole, their polymerisation and incorporation into novel composite gas sensitive resistors

3-Octadecylpyrrole and the novel 3-docosylpyrrole were synthesised in high yields. These monomers were polymerised with various oxidising agents to produce a range of 3-octadecylpolypyrroles and 3-docosylpolypyrroles with different counter-ions. These polymers were soluble in chloroform and were readily coated onto microporous poly(vinylidene fluoride) membranes. Novel 3-alkylpolypyrrole–tin(IV) oxide composites were also produced by adding finely ground tin(IV) oxide to a solution of the 3-alkylpolypyrrole in chloroform and drop-coating the resulting mixture onto alumina substrates or poly(vinylidene fluoride) membranes. The resulting 3-alkylpolypyrrole based materials were tested for their gas sensitivity towards a number of classes of volatile organic compounds (VOCs). The 3-alkylpolypyrrole–tin(IV) oxide composites were found to exhibit enhanced sensitivity and differing selectivities to VOCs when compared to tin(IV) oxide or the 3-alkylpolypyrrole alone. Previously, conducting polymers exhibited little response to non-polar VOCs, in contrast 3-octadecylpolypyrrole-nitrate–tin(IV) oxide composite sensors were particularly sensitive to hydrocarbons and could detect butane and propane at concentrations well below their lower limit of explosion (LLE).

Sorptive interactions between VOCs and indoor materials.

This study was carried out using various materials (carpet, gypsum board, upholstery, vinyl and wood flooring, acoustic tiles, and fruit) that were exposed to eight gaseous volatile organic compounds (VOCs) (isopropanol, MTBE, cyclohexane, toluene, ethylbenzene, tetrachloroethene, 1,2-dichlorobenzene, and 1,2,4-trichlorobenzene) in electro-polished stainless-steel chambers. Dynamic responses in VOC concentrations were used to determine linear adsorption and desorption rate coefficients and equilibrium partition coefficients. A linear adsorption/desorption model was used to effectively describe the interactions between VOCs and indoor surface materials for short-term source events (10 h). Relationships between sorption parameters and chemical vapor pressure and the octanol-air partition coefficient were observed. Carpet was identified as the most significant sorptive sink for non-polar VOCs. Virgin gypsum board was observed to be a significant sink for highly polar VOCs. Sorptive interactions between non-polar VOCs and indoor materials were not affected by variations in relative humidity. However, increases in relative humidity were observed to increase the degree of sorption of isopropanol to carpet.

Survey of volatile organic compounds associated with automotive emissions in the urban airshed of São Paulo, Brazil

The Metropolitan Region of São Paulo (MRSP), Brazil, is one of the largest metropolitan areas in the world (population 17 million, approx.) and relies heavily on alcohol-based fuels for automobiles. It is estimated that about 40% of the total volume of fuel is ethanol with some vehicles using pure ethanol and others a gasoline/ethanol blend. As such, São Paulo is an excellent example of an oxygenates-dominated airshed of mobile sources and is most likely indicative of the future in heavily populated areas in the US such as Los Angeles where “oxy-fuels” are becoming an important replacement for the conventional pure petroleum-based fuels. In this work, we surveyed the ambient air to identify and quantify the organic compounds associated with the evaporative and exhaust emissions of these fuels and to begin to understand the potential for human exposure. Because this was an initial test without detailed prior knowledge of the airshed of the area, we applied two different air sampling methods for various time periods to assess the ambient concentrations of a variety of polar and nonpolar volatile organic compounds (VOCs). For quality assurance (QA), we collected all the samples in duplicate (whole-air samples in Summa canisters and adsorbent-based samples on Perkin-Elmer Air Toxics tubes) at various flow rates to test performance. All samples were collected over identical time frames, typically for 1-, 2-, and 4-h periods per day at six different locations over a period of 1 week. Overall São Paulo results demonstrate that mean concentrations of single-ring aromatics are 2–3 times higher, volatile aldehydes are 5–10 times higher, and simple alcohols 10–100 times higher as compared to results of a recent study performed by EPA in the Los Angeles basin. C 4–C 11 n-alkanes were only slightly elevated in São Paulo.

CHARACTERIZATION OF VOLATILE ORGANIC COMPOUNDS IN SMOKE AT EXPERIMENTAL FIRES

Significant associations between firefighting and cancer have been reported; however, studies finding toxic products of combustion at municipal fires have been limited by (1) technical difficulties encountered at the scene of working fires, (2) the lack of a coherent sampling strategy, and (3) the absence of verified sampling methods. The objective of the present study was to characterize the presence of volatile organic compound (VOC) combustion products in fire smoke. Air samples from experimental fires burning various materials commonly found at structural fires were collected into evacuated Summa canisters and analyzed for 144 target VOCs using cryogenic preconcentration and gas chromatography/mass spectroscopy (GC/MSD) methodology. The resulting chromatograms were characterized by a small number of predominant peaks, with 14 substances (propene, benzene, xylenes, 1-butene/2-methylpropene, toluene, propane, 1,2-butadiene, 2-methylbutane, ethylbenzene, naphthalene, styrene, cyclopentene, 1-methylcyclopentene, isopropylbenzene) being found in proportionately higher concentrations in all experimental fires and accounting for 65% (SD = +/-12%) by mass of total measured VOCs. Benzene, toluene, 1,3-butadiene, naphthalene, and styrene were found at higher concentrations than most other VOCs and increased with the time of combustion together with increasing levels of carbon monoxide. Benzene was found in the highest concentrations, with peak levels ranging from 0.6 ppm to 65 ppm, while the levels of 1,3-butadiene, styrene, and naphthalene peaked at 0.1, 0.4, and 3 ppm, respectively. This study revealed that there were no new or novel, toxic nonpolar VOCs resulting from the burning of common building materials. This is important in view of the studies that have found associations between firefighting and various forms of cancer.