Water-soluble Volatile Organic Compounds Research Articles

Construction of PTFE/PI-PI/PANI-PA composite nanofibrous membrane for efficient photothermal membrane distillation and VOCs interception

Water-soluble volatile organic compounds (VOCs) are one of the difficult substances in seawater and industrial wastewater treatment. Photothermal membrane distillation (PMD) technology has great advantages in solving the problems of low energy conversion efficiency and serious pollution of traditional membrane distillation (MD) technology, but it still faces the challenge that VOCs cannot be effectively removed.To solve this problem, we prepared photothermal Polytetrafluoroethylene/Polyimide-Polyimide/Polyaniline-Polyamide (PTFE/PI-PI/PANI-PA) composite membranes with VOCs interception. The composite membrane was fabricated by applying the previously studied PTFE/PI-PI/PANI/PANI membrane by interfacially polymerising an ultrathin PA layer with controllable pore sizes. Among them, the PTFE/PI-PI/PANI base membrane in the composite membrane not only provides strong support and durability as a backbone structure, but the PANI photothermal layer also provides photothermal conversion for effective PMD operation. In addition, the ultra-thin PA layer acts as a molecular sieve separator to effectively intercept VOCs in the feed solution. When the feed solution was 35 g⋅L−1 NaCl, the average permeate flux of the #M-PA-0.1 membrane was 1.44 ± 0.02 L⋅m−2⋅h−1 with a salt interception rate of 99.99 % or more after 80 h of PMD testing. Meanwhile, when 50 mg⋅L−1 of VOCs was added to the feed solution, the VOCs retention rate >99.35 %, and the concentration of VOCs on the permeate side was much lower than the corresponding concentration in the drinking water standards recommended by the World Health Organisation (WHO) and the US Environmental Protection Agency (EPA). This study effectively combines the molecular sieve effect with the solar-powered evaporation process, which provides a research basis for the preparation of high-performance PMD membranes that can effectively remove volatile organic compounds.

Development of a Moisture Pretreatment Device for the Accurate Quantitation of Water-Soluble Volatile Organic Compounds in Air

In air pollutant monitoring using sensors, moisture can adversely affect the analytical accuracy of volatile organic compounds (VOCs). Therefore, a new moisture pretreatment device (KPASS–Odor) for analyzing VOCs in the air was developed, based on frost and created by a desublimation process inside a cold tube. The performance of KPASS–Odor was compared with conventional devices (i.e., a NafionTM dryer and a cooler) through the measurements of low water-soluble VOCs (i.e., benzene, toluene, ethyl benzene, p-xylene, and styrene) and relatively high ones (i.e., methyl-ethyl ketone, methyl isobutyl ketone, butyl acetate, and isobutyl alcohol) using gas chromatography (GC) and sensor methods. Regarding the GC method, the recovery rates for KPASS–Odor and the cooler were >95% and >80%, respectively, at a flow rate of 500 mL/min for all compounds. For the NafionTM dryer, the recovery rates differed between low and high water-soluble compounds, which exhibited the rates ≥88% and ≤86%, respectively. In terms of the sensor method, the VOC recovery rates of KPASS–Odor and the NafionTM dryer were found to be >90% and <50%, respectively. Therefore, KPASS–Odor was determined to be the most suitable moisture pretreatment device for highly soluble VOCs of concern in this study.

Ultra-trace detection and efficient adsorption removal of multiple water-soluble volatile organic compounds by fluorescent sensor array.

Due to the extremely low concentration, complex composition and easy to be converted into each other in water and air of water-soluble volatile organic compounds (VOCs), it is a great challenge to the traditional detection technology, pollution control and traceability, etc. Therefore, developing a convenient, swift and on-site detection method for simultaneous quantification of multiple VOCs is highly anticipated. In this paper, a multifunctional sensor array with adsorption and sensing of VOCs has been constructed by four fluorescence channels of small-sized Eu@Uio-66 and Tb@Uio-66. Due to the obvious cross-reactive characteristics between 4 fluorescence channels and VOCs, the sensor array could detect 8 VOCs simultaneously with all detection limits as low as ppb level. In addition, the detection results of sensor array for actual water samples coexisting with multiple VOCs confirmed that it has strong anti-interference performance and could be used for simultaneous detection of multiple VOCs in real water. The construction of sensor array with VOC adsorption function not only helps to reduce the detection limit of VOCs benefiting from the pre-concentration of materials, but also has significant value to reduce the harmfulness of pollutants. Predictably, this work is of great significance for VOC traceability, analysis of ecotoxicological effects and monitoring of pollution distribution characteristics.

Metal-Organic Framework Composite Photothermal Membrane for Removal of High-Concentration Volatile Organic Compounds from Water via Molecular Sieving.

Water-soluble volatile organic compounds (VOCs) are among the most difficult-to-treat species during wastewater treatment. The current purification and removal of high-concentration VOCs still rely on the energy-consuming distillation and high-pressure driven reverse osmosis technology. There is an urgent need for an advanced technology that can effectively remove high-concentration VOCs from water. Here, we report a metal-organic framework (MOF)/polyaniline (PANI) nanofiber array composite photothermal membrane for removal of high-concentration VOCs from water via molecular sieving during a solar-driven evaporation process. The modified zeolitic imidazole framework-8 (ZIF-8) layer grown on a PANI nanofiber array acts as a molecular sieving layer to evaporate water but intercept VOCs. The composite membrane exhibits high VOCs rejection and a high-water evaporation rate for water containing different concentrations of VOCs. When treating water containing VOCs with a concentration of up to 400 mg L-1, the VOCs rejection rate is up to 99% and the water evaporation rate is 1.0 kg m-2 h-1 under 1 sun irradiation (1 kW m-2). Our work effectively combines the molecular sieve effect with a solar-driven evaporation process, which provides an effective strategy for the treatment of water containing VOCs.

Super Water‐Extracting Gels for Solar‐Powered Volatile Organic Compounds Management in the Hydrological Cycle

Water-soluble volatile organic compounds (VOCs) are widely spread in the natural hydrological cycle, contaminating potential water sources, and leading to unexpected ecological hazards. However, water-purification technologies toward VOCs are energy-intensive and present unsatisfactory purity of the obtained water. The fundamental challenge is to differentiate the motion of water and VOC molecules by separators. Here, the concept of a super water-extracting gel (SWEG) for VOC-management and water purification via direct solar distillation is proposed. The strong hydrogen bonding effect in the hypercrosslinked hydrophilic polymeric networks enables the SWEG to extract water from VOC-containing water, which rejects the VOC solutes while allowing water through for interfacial evaporation. The obtained SWEG achieves a VOCs removal ratio up to 99.99% by solar distillation under 1 sun. A solar water-purification system is also demonstrated to produce clean water, which surpasses other competitive technologies based on electricity.

Decomposition of 2-Propanol in the Liquid Phase Using a Photocatalyst Immobilized on Nonwoven Fabric and Ozone Microbubbles

2-Propanol (IPA) is a highly water-soluble volatile organic compound that is used in the cleaning and drying processes during semiconductor fabrication. IPA is also used as a disinfectant in the pharmacy field. Water scrubber processing is one of the methods used for IPA collection. However, water scrubbing requires wastewater treatment. In this study, we propose a decomposition system for IPA in the liquid phase based on a TiO2 photocatalyst immobilized on nonwoven fabric (TiO2 nonwoven fabric) and ozone microbubbles (MBs). The thick nonwoven fabric with immobilized TiO2 exhibits a higher IPA removal rate than that exhibited by the pleated fabric. IPA decomposes to produce acetone, which can be further decomposed and possibly undergo mineralization. The entire water tank can be supplied with ozone by introducing the MB-forming ozone, which considerably affects the decomposition of IPA. The efficient decomposition of IPA was achieved by combining ozone MBs, TiO2 nonwoven fabric, and ultraviolet irradiation, presumably because the photocatalyst promotes the mineralization of the decomposition product. Thus, the OH radicals from the O3 MBs competitively captured in the decomposition product strongly promote the decomposition of IPA, enhancing the IPA decomposition rate.

Uptake of nitric acid, ammonia, and organics in orographic clouds: mass spectrometric analyses of droplet residual and interstitial aerosol particles

Abstract. Concurrent in situ analyses of interstitial aerosol and cloud droplet residues have been conducted at the Schmücke mountain site during the Hill Cap Cloud Thuringia campaign in central Germany in September and October 2010. Cloud droplets were sampled from warm clouds (temperatures between −3 and +16 °C) by a counterflow virtual impactor and the submicron-sized residues were analyzed by a compact time-of-flight aerosol mass spectrometer (C-ToF-AMS), while the interstitial aerosol composition was measured by an high-resolution time-of-flight aerosol mass spectrometer (HR-ToF-AMS). During cloud-free periods, the submicron out-of-cloud aerosol was analyzed using both instruments, allowing for intercomparison between the two instruments. Further instrumentation included black carbon measurements and optical particle counters for the aerosol particles as well as optical sizing instrumentation for the cloud droplets. The results show that, under cloud conditions, on average 85 % of the submicron aerosol mass partitioned into the cloud liquid phase. Scavenging efficiencies of nitrate, ammonium, sulfate, and organics ranged between 60 and 100 %, with nitrate having, in general, the highest values. For black carbon, the scavenging efficiency was markedly lower (about 24 %). The nitrate and ammonium mass fractions were found to be markedly enhanced in cloud residues, indicating uptake of gaseous nitric acid and ammonia into the aqueous phase. This effect was found to be temperature dependent: at lower temperatures, the nitrate and ammonium mass fractions in the residues were higher. Also, the oxidation state of the organic matter in cloud residues was found to be temperature dependent: the O : C ratio was lower at higher temperatures. A possible explanation for this observation is a more effective uptake and/or higher concentrations of low-oxidized water-soluble volatile organic compounds, possibly of biogenic origin, at higher temperatures. Organic nitrates were observed in cloud residuals as well as in the out-of-cloud aerosol, but no indication of a preferred partitioning of organic nitrates into the aqueous phase or into the gas phase was detected. Assuming the uptake of nitric acid and ammonia in cloud droplets will be reversible, it will lead to a redistribution of nitrate and ammonium among the aerosol particles, leading to more uniform, internally mixed particles after several cloud passages.

Secondary organic aerosol formation from isoprene photooxidation during cloud condensation–evaporation cycles

Abstract. The impact of cloud events on isoprene secondary organic aerosol (SOA) formation has been studied from an isoprene ∕ NOx ∕ light system in an atmospheric simulation chamber. It was shown that the presence of a liquid water cloud leads to a faster and higher SOA formation than under dry conditions. When a cloud is generated early in the photooxidation reaction, before any SOA formation has occurred, a fast SOA formation is observed with mass yields ranging from 0.002 to 0.004. These yields are 2 and 4 times higher than those observed under dry conditions. When the cloud is generated at a later photooxidation stage, after isoprene SOA is stabilized at its maximum mass concentration, a rapid increase (by a factor of 2 or higher) of the SOA mass concentration is observed. The SOA chemical composition is influenced by cloud generation: the additional SOA formed during cloud events is composed of both organics and nitrate containing species. This SOA formation can be linked to the dissolution of water soluble volatile organic compounds (VOCs) in the aqueous phase and to further aqueous phase reactions. Cloud-induced SOA formation is experimentally demonstrated in this study, thus highlighting the importance of aqueous multiphase systems in atmospheric SOA formation estimations.

SimpleGAMMA v1.0 – a reduced model of secondary organic aerosol formation in the aqueous aerosol phase (aaSOA)

Abstract. There is increasing evidence that the uptake and aqueous processing of water-soluble volatile organic compounds (VOCs) by wet aerosols or cloud droplets is an important source of secondary organic aerosol (SOA). We recently developed GAMMA (Gas–Aerosol Model for Mechanism Analysis), a zero-dimensional kinetic model that couples gas-phase and detailed aqueous-phase atmospheric chemistry for speciated prediction of SOA and organosulfate formation in cloud water or aqueous aerosols. Results from GAMMA simulations of SOA formation in aerosol water (aaSOA) (McNeill et al., 2012) indicate that it is dominated by two pathways: isoprene epoxydiol (IEPOX) uptake followed by ring-opening chemistry (under low-NOx conditions) and glyoxal uptake. This suggested that it is possible to model the majority of aaSOA mass using a highly simplified reaction scheme. We have therefore developed a reduced version of GAMMA, simpleGAMMA. Close agreement in predicted aaSOA mass is observed between simpleGAMMA and GAMMA under all conditions tested (between pH 1–4 and RH 40–80 %) after 12 h of simulation. simpleGAMMA is computationally efficient and suitable for coupling with larger-scale atmospheric chemistry models or analyzing ambient measurement data.

The Atmosphere can be a Source of Certain Water Soluble Volatile Organic Compounds in Urban Streams

AbstractSurface water and air volatile organic compound (VOC) data from 10 U.S. Geological Survey monitoring sites were used to evaluate the potential for direct transport of VOCs from the atmosphere to urban streams. Analytical results of 87 VOC compounds were screened by evaluating the occurrence and detection levels in both water and air, and equilibrium concentrations in water (Cws) based on the measured air concentrations. Four compounds (acetone, methyl tertiary butyl ether, toluene, and m‐ & p‐xylene) were detected in more than 20% of water samples, in more than 10% of air samples, and more than 10% of detections in air were greater than long‐term method detection levels (LTMDL) in water. Benzene was detected in more than 20% of water samples and in more than 10% of air samples. Two percent of benzene detections in air were greater than one‐half the LTMDL in water. Six compounds (chloroform, p‐isopropyltoluene, methylene chloride, perchloroethene, 1,1,1‐trichloroethane, and trichloroethene) were detected in more than 20% of water samples and in more than 10% of air samples. Five VOCs, toluene, m‐ & p‐xylene, methyl tert‐butyl ether (MTBE), acetone, and benzene were identified as having sufficiently high concentrations in the atmosphere to be a source to urban streams. MTBE, acetone, and benzene exhibited behavior that was consistent with equilibrium concentrations in the atmosphere.

Characterization of the University of Toronto Concentrated Aerosol Particle Exposure Facility (CAPEF)—Effects on Fine and Ultrafine Nonrefractory Aerosol Composition

Virtual impactor-based particle concentrators have been developed to enable the study of biological mechanisms and dose-response relationships of particulate matter (PM) inhalation. The Concentrated Aerosol Particle Exposure Facility (CAPEF) at the University of Toronto houses the Harvard School of Public Health designed coarse, fine, and quasi-ultrafine particle concentrators for such studies. Characterization of the concentration of the nonrefractory components of ambient particles was carried out in the winter of 2010. The fine concentrator shows higher mass concentration factors for ambient sulfate than for semi-volatile components, as measured using an Aerodyne aerosol mass spectrometer (AMS). The change in composition is based on the relative size distributions of particulate sulfate, which, compared to particulate organic and nitrate, is more dominant in larger particles more efficiently concentrated due to the physical characteristics of the virtual impactors. The ultrafine concentrator, which requires aqueous condensational growth of particles prior to concentration, shows a large enhancement in organic mass both for ambient particles and for laboratory-generated ammonium sulfate and ammonium nitrate particles added to filtered outdoor air. As suggested previously, changes in the organic mass spectrum and size distributions are consistent with addition of organic mass through reactions of water-soluble volatile organic compounds. Coagulation of particles or droplet coalescence may also account for some of the observed increase in organic mass and nitrate may be lost due to volatilization. While such effects are unlikely to affect refractory species, increased attention should be given to the effect of condensational growth on the composition of concentrated ultrafine particles. Copyright 2012 American Association for Aerosol Research

Water content of pyrolysis oil: Comparison between Karl Fischer titration, GC/MS-corrected azeotropic distillation and 1H NMR spectroscopy

Pyrolysis converts biomass waste mainly into pyrolysis oil, which is a possible source of renewable energy and/or value-added chemicals. A very important characteristic of pyrolysis oil is its water content. Karl Fischer titration and azeotropic distillation by the Dean-Stark method are two common techniques for water determination. In this study, the water content is determined for several pyrolysis oil samples with a wide range in water content and/or originating from different types of biomass. The results of the conventional techniques are compared with these of a new proposed technique based on 1H NMR spectroscopy.Azeotropic distillation turns out to be very sensitive for overestimation of the water content in case of pyrolysis oils with high amount of water soluble volatile organic compounds. Therefore, a GC/MS-correction is applied to these results. After correction, the results of the azeotropic distillation are in good agreement with these of the Karl Fischer titration. This strongly indicates that Karl Fischer titration and GC/MS corrected azeotropic distillation are free of interferences for the investigated pyrolysis oil samples, since similar results are obtained by two independent methods. The results of the 1H NMR spectroscopy are very comparable with these of the conventional techniques for the oil samples with low and intermediate water content (<50wt%). Only for samples with very high water content, 1H NMR gives an underestimation in comparison with the conventional techniques. Hence, 1H NMR spectroscopy is a possible alternative water determination technique for most pyrolysis oils.

Biofiltration of hydrophobic VOCs pretreated with UV photolysis and photocatalysis

The effects of pretreatments on the biofiltration of gas phase α-pinene, a poorly water soluble Volatile Organic Compound (VOC), was evaluated in a controlled and long-term experimental investigation. Ultraviolet (UV) photolysis and photocatalysis were used and compared as pretreatment techniques. A control experiment involving biofiltration alone allowed for the direct evaluation of the coupled UV-biofiltration. α-Pinene contaminated streams with flow rates of 5?6.5 l/min and concentrations of up to 130 ppmv were passed through the systems. UV pretreatment on average converted between 20 and 50% of α-pinene into water soluble intermediates. When comparing the effectiveness of each pretreatment process, UV photocatalysis provided greater α-pinene conversion, especially at low retention times and high contaminant loading. The untreated α-pinene along with the by-products of UV photooxidation was then removed effectively in the biofiltration stage. The UV-biofiltration process offered 50?80% more α-pinene removal compared to the control biofilter. Regardless of their effectiveness at removing the contaminant, photolysis and photocatalysis pretreatments had similar synergistic impact on the performance of the downstream biofilter.

Analysis of VOCs in Ambient Air Using Multisorbent Packings for VOC Accumulation and Sample Drying

Abstract Solid multisorbent packings have been characterized for trapping and release efficiency of trace (10-20 ppbv in humidified zero air) volatile organic compounds (VOCs). The use of a two-stage trapping system reduces sample water content typically by more than 95.5% while maintaining a trapping and release efficiency of 100% for 49 VOCs, including eight water-soluble VOCs. Three combinations of primary tube and focusing tube are examined in detail by using an atomic emission detector to monitor hydrogen as an indication of residual water vapor, and to monitor either chlorine, bromine, or carbon for target VOCs. Linearity of response to individual VOCs, the presence of artifacts, and a laboratory monitoring application are also discussed.

Concentration of water-soluble volatile organic compounds from aqueous samples by azeotropic microdistillation

Methanol and other similar water-soluble volatile organic compounds in zero headspace extracts and other aqueous matrices can be analyzed by azeotropic microdistillation, followed by gas chromatographic separation and detection. The method detection limits for methanol, 1-butanol (n-butyl alcohol), and 2-methyl-1-propanol (isobutyl alcohol) are at least 1 order of magnitude below the current land disposal treatment standards using the toxicity characteristic leaching procedure (TCLP)