Absorption Of Volatile Organic Compounds Research Articles

Volatile organic compounds absorption in a structured packing fed with waste oils: Experimental and modeling assessments

Volatile Organic Compounds (VOCs) having different polarities were absorbed in two viscous waste oils (a transformer oil and a lubricant, whose viscosities are equal to 19 mPa s and 79 mPa s, respectively) in a structured packing (1 m height) operated at counter-current. A synthetic hydrophobic solvent (PDMS 20, a silicone oil) and water were also used as reference solvents. Removal efficiencies of hydrophobic VOCs in silicone and transformer oils up to 80–90% were measured. Nonetheless, owing to a higher viscosity, the removal efficiencies in the lubricant were significantly lower. A deconvolution procedure, based on the Higbie penetration theory, was developed to deduce the local mass transfer coefficients (kL and kG) from KLa° values. These local coefficients were compared to the predictions of the models of Billet-Schultes (BS) and Song-Seibert-Rochelle (SSR), allowing to conclude that the SSR model better addresses the influence of the viscosity on KLa° than the BS model.

Reversible Absorption of Volatile Organic Compounds by Switchable-Hydrophilicity Solvents: A Case Study of Toluene with N,N-Dimethylcyclohexylamine.

Absorption is one of the most important treatment technologies for the removal of volatile organic compounds (VOCs) from tail gases, yet the separation of the absorbents and VOCs remains challenging because of concerns related to environmental impact and large energy requirements. Herein, we explored an absorption and desorption process using N,N-dimethylcyclohexylamine (CyNMe2) as a representative switchable-hydrophilicity solvent (SHS) and toluene as a representative VOC. The results showed that in comparison to common absorbents, CyNMe2 exhibits excellent toluene absorption performance. Desorption efficiencies of toluene from CyNMe2 of up to 94% were achieved by bubbling CO2 at 25 °C, and separation efficiencies of CyNMe2 from water up to 90% were achieved by bubbling N2 at 60 °C. Even after five absorption–desorption cycles, the toluene absorption capacity of CyNMe2 was comparable with that of the fresh absorbent, suggesting that CyNMe2 retains its absorption capacity. We demonstrate an innovative and reversible remediation strategy of VOCs based on SHSs, and the results indicate that SHSs can be used as an alternative to common absorbents for the removal of VOCs to reduce environmental pollution and energy consumption.

Self-assembly Cu2O nanowire arrays on Cu mesh: A solid-state, highly-efficient, and stable photocatalyst for toluene degradation under sunlight

Sunlight driven photocatalysis offers an effective and eco-friendly technology for volatile organic compounds (VOCs) removal. Three dimensional (3D) and oriented structure can facilitate efficient photon absorption and rapid diffusion of VOCs, which prevails over the powder-formed catalysts. Herein, free-standing and uniform p-type Cu2O nanowire (NW) arrays were obtained through heat treatment of Cu(OH)2 NWs, which were spontaneously grown from Cu mesh in air under room temperature for the first time. The as-prepared Cu2O NWs show excellent degradation performance in decomposing 30 ppm toluene (99.9 % within 120 min) and high stability (no decline after ten recycles). The toluene degradation was also conducted under the natural sunlight, demonstrating complete removal from 12:00 am to 15:00 pm. During photocatalysis, toluene is attacked by the photogenerated holes (h+) and hydroxyl radicals (·OH), and finally oxidized to nontoxic small molecules. The photocatalytic removing toluene with Cu2O NWs/Cu mesh has a promising application prospect owing to its low cost, high efficiency, stability, and convenient operation.

Study of the toluene absorption capacity and mechanism of ionic liquids using COSMO-RS prediction and experimental verification

As green solvents, ionic liquids (ILs) are quite suitable for the absorption of volatile organic compounds (VOCs) such as benzene and its homologues. However, solvent selection is the key to the VOC absorption process. In the present study, a rapid solvent screening tool, Conductor-like Screening Model for Real Solvents (COSMO-RS), was used to predict the solubility of toluene in 816 ILs. The effects of four structure characters, namely, the type and alkyl chain length of the cations and anions on the solubility of toluene were discussed. The following conclusions were drawn from the results: (1) ILs with pyrrolidinium-based cations showed better solubility than pyridinium- and imidazolium-based ones. (2) The solubility of toluene in PF6-based ILs increased with the increasing alkyl chain length, while its solubility in Ac-based ILs exhibited the opposite trend. (3) Toluene showed greater solubility in Cl-based ILs than those based on other anions. (4) The solubility of toluene increased with the anion alkyl chain length. Ac-based ILs were chosen as the most promising potential solvents, and further studied to determine the relationship between various interaction energy parameters and toluene solubility. The results showed that the misfit energy played a dominant role during the absorption process. Furthermore, several ILs were selected for experimental verification of the predicted solubility behavior using liquid and gaseous toluene. The results demonstrated that COSMO-RS could be used to semi-quantitatively and qualitatively predict the solubility of toluene, and this model had promising prospects in screening ILs for VOCs absorption. In summary, this study provided a fundamental basis and practical data for the control and treatment of VOCs.

Development of a simulation chamber for the evaluation of dermal absorption of volatile organic compounds

An exposition chamber has been designed and developed for the production of contaminated atmospheres with fixed and known concentration of volatile organic compounds. The proposed chamber has been evaluated for the determination of in-vitro diffusion parameters, such as flux and lag time for benzene, toluene, ethylbenzene, and xylenes (BTEX). Polydimethylsiloxane (PDMS) and Strat-M® membranes were evaluated, including the effect of membrane thickness, from 0.5 to 3.0 mm, on the diffusion parameters. The obtained flux values and lag times, ranged from 0.2 to 1.5 μg cm−2 h−1 and from 10 to 130 min, respectively, for studies performed at a BTEX concentration of 51 μg L−1 in air. Different air concentration of BTEX were evaluated in the calibration chamber, indicating that flux increased proportionally to the BTEX concentration in air and the lag time decreased as the air concentration of BTEX increased.

Molasses Grass Induces Direct and Indirect Defense Responses in Neighbouring Maize Plants.

Plants have evolved intricate defence strategies against herbivore attack which can include activation of defence in response to stress-related volatile organic compounds (VOCs) emitted by neighbouring plants. VOCs released by intact molasses grass (Melinis minutiflora), have been shown to repel stemborer, Chilo partellus (Swinhoe), from maize and enhance parasitism by Cotesia sesamiae (Cameron). In this study, we tested whether the molasses grass VOCs have a role in plant-plant communication by exposing different maize cultivars to molasses grass for a 3-week induction period and then observing insect responses to the exposed plants. In bioassays, C. partellus preferred non-exposed maize landrace plants for egg deposition to those exposed to molasses grass. Conversely, C. sesamiae parasitoid wasps preferred volatiles from molasses grass exposed maize landraces compared to volatiles from unexposed control plants. Interestingly, the molasses grass induced defence responses were not observed on hybrid maize varieties tested, suggesting that the effect was not simply due to absorption and re-emission of VOCs. Chemical and electrophysiological analyses revealed strong induction of bioactive compounds such as (R)-linalool, (E)-4,8-dimethyl-1,3,7-nonatriene and (E,E)-4,8,12-trimethyl-1,3,7,11-tridecatetraene from maize landraces exposed to molasses grass volatiles. Our results suggest that constitutively emitted molasses grass VOCs can induce direct and indirect defence responses in neighbouring maize landraces. Plants activating defences by VOC exposure alone could realize enhanced levels of resistance and fitness compared to those that launch defence responses upon herbivore attack. Opportunities for exploiting plant-plant signalling to develop ecologically sustainable crop protection strategies against devastating insect pests such as stemborer C. partellus are discussed.

Adsorption of volatile organic compounds on modified spherical activated carbon in a new cyclonic fluidized bed

Volatile organic compounds (VOCs) are severe environmental pollutants that pose a serious threat to human health. In this study, a new type of cyclonic fluidized bed was designed to carry out absorption of VOCs by activated carbon, in which the collision and adsorption between activated carbon particles and VOC moleculars were enhanced by three-dimensional rotating turbulent shear. We studied the VOC adsorption efficiency of three kinds of modified spherical activated carbon (SAC-1, SAC-2, and SAC-3) and five kinds of cyclonic fluidized bed (S11-44, S11-33, S11-22, S13-22, and S16-22). The pressure drop of the cyclonic fluidized bed under different inlet flow rates, activated carbon dosages, and inlet VOC concentrations were also investigated. The results indicate that smaller inlet flow rate, larger activated carbon dosage, larger diameter and smaller inserted depth of the cyclone fluidized bed overflow pipe will lead to lower pressure drop and higher VOCs adsorption efficiency. The pitch-based SAC-1 and the S16-22 cyclonic fluidized bed had the highest adsorption efficiency (100%) and the lowest pressure drop (120 Pa). This study not only benefits VOC absorption but also serves as a useful guide for the development of cyclone separation technology in industrial processes.

Firefighters’ absorption of PAHs and VOCs during controlled residential fires by job assignment and fire attack tactic

To better understand the absorption of combustion byproducts during firefighting, we performed biological monitoring (breath and urine) on firefighters who responded to controlled residential fires and examined the results by job assignment and fire attack tactic. Urine was analyzed for metabolites of polycyclic aromatic hydrocarbons (PAHs) and breath was analyzed for volatile organic compounds (VOCs) including benzene. Median concentrations of PAH metabolites in urine increased from pre-firefighting to 3-h post firefighting for all job assignments. This change was greatest for firefighters assigned to attack and search with 2.3, 5.6, 3.9, and 1.4-fold median increases in pyrene, phenanthrene, naphthalene, and fluorene metabolites. Median exhaled breath concentrations of benzene increased 2-fold for attack and search firefighters (p < 0.01) and 1.4-fold for outside vent firefighters (p = 0.02). Compared to interior attack, transitional attack resulted in 50% less uptake of pyrene (p = 0.09), 36% less uptake phenanthrene (p = 0.052), and 20% less uptake of fluorene (p < 0.01). Dermal absorption likely contributed to firefighters’ exposures in this study. Firefighters’ exposures will vary by job assignment and can be reduced by employing a transitional fire attack when feasible.

KLa Determination Using the Effectiveness-NTU Method: Application to Countercurrent Absorbers in Operation Using Viscous Solvents for VOCs Mass Transfer

In this study, the Effectiveness-NTU method, which is usually applied to heat exchanger design, was adapted to gas–liquid countercurrent absorbers to determine the overall mass transfer coefficient, KLa, of the apparatus in operation. It was demonstrated that the ε-NTU method could be used to determine the KLa using the Henry coefficient of the solute to be transferred (HVOC), the gas flow-rate (QG), the liquid flow-rate (QL), the scrubber volume (V), and the effectiveness of the absorber (ε). These measures are calculated from the gaseous concentrations of the solute measured at the absorber inlet (CGin) and outlet (CGout), respectively. The ε-NTU method was validated from literature dedicated to the absorption of volatile organic compounds (VOCs) by heavy solvents. Therefore, this method could be a simple, robust, and reliable tool for the KLa determination of gas–liquid contactors in operation, despite the type of liquid used, i.e., water or viscous solvents.

Assessment of VOC absorption in hydrophobic ionic liquids: Measurement of partition and diffusion coefficients and simulation of a packed column

Partition coefficients of toluene and dichloromethane (DCM) in 23 hydrophobic ionic liquids (ILs), which can be used potentially for the physical absorption of volatile organic compounds (VOCs), were measured at 298 K. The partition coefficients, expressed as Henry’s law constants, were 400–1300 times for toluene and 10–47 times for DCM lower in the selected ILs than in water. Thus, the toluene and DCM diffusion coefficients were measured in three high potential hydrophobic ILs and in [Bmim][NTf2] using a thermogravimetric microbalance. Diffusivity measurements were performed at 298 K for toluene and between 278 and 308 K for DCM. Diffusion coefficients in ILs, ranging between 1 and 4 × 10−11 m2 s−1, were from 18 to 90 times lower than in water at 298 K. The diffusion coefficients were correlated to the temperature, the solute molar volume, the IL viscosity and molar volume with an average error of 4.2%. Finally, a 3 m industrial packed column was simulated for the removal of DCM and toluene in [AllylEt2S][NTf2] and [bmim][NTf2], which both present moderate viscosities of nearly 50 mPa s at 293 K. The overall mass-transfer coefficient, the removal efficiency and the pressure drop were calculated and compared to those obtained using other heavy solvents (a silicon oil and di-(2-ethylhexyl) adipate). This prospective simulation has demonstrated a good potential of ionic liquids for the toluene removal. Nonetheless, the DCM removal efficiencies simulated were lower than 44%. It suggests that even more efficient ionic liquids can be tuned and synthesized in the future for this specific application.

Recent Advancements in Method Development and Exposure Assessment for 45 Blood VOCs Analyzed by Headspace SPME GC-MS

For over three decades our laboratory has been developing and improving methods for quantifying toxic volatile organic compounds (VOCs) in blood in support of numerous national and regional studies, including nine National Health and Nutrition Examination Survey (NHANES) cycles. Absorption of VOCs most commonly occurs through inhalation, as 100% of blood circulates to the lungs for exchange with alveolar gas. The high blood:gas partition ratios of most VOCs favor preconcentration in the blood, but blood VOC equilibration with tissues and organs is what influences VOC elimination half-life. As such, VOC analysis in blood is best-suited for compounds that are stable in the body by offering a direct measure of VOC burden experienced by tissues and organs.The current analysis method uses headspace solid-phase microextraction (HS-SPME) and gas chromatography-mass spectrometry (GC-MS). Important to the success of this method is the use of isotopically labeled analogs specific to every compound to compensate for competition effects in the headspace and SPME fiber, as well as adsorption and volatilization losses. The combination of these techniques has enabled us to simultaneously quantify a broad array of VOCs (boiling points from 32 to 204 &amp;#176;C) in the low parts-per-trillion (ng/L) range from a 3-mL blood sample.This presentation will include an overview of the blood VOC method and describe recent improvements to achieve accuracy and precision of &amp;lt; 15% for nonpolar compounds (e.g., alkanes) and within 5% for most of the other VOCs. We will also describe noteworthy blood VOC trends in the United States and reveal new analytes that are to be included in future studies and NHANES cycles. In addition to individual VOC trends, we will describe recent work comparing relative VOC levels among participants using artificial neural networks as a means to objectively distinguish exposure between different VOC sources within a large population.

Using aligned poly(3-hexylthiophene)/poly(methyl methacrylate) blend fibers to detect volatile organic compounds

In this study, we developed a novel sensing material fabricated using a poly(3-hexylthiophene) (P3HT)/poly(methyl methacrylate) (PMMA) blend fiber on a glass substrate. The sensing materials can easily be used for sensing toluene vapor detected from extinction spectral changes. The extinction spectra variation is noted from the absorption of volatile organic compounds in a highly specific surface area of fibrous coating. An electrospinning technique is applied to generate a nonwoven structure and uniaxial orientation by fibrous coating. The response of the uniaxially orientated fibrous film is even improved at several toluene vapor concentrations. The best detection limit of this well-aligned fibrous film is up to 200 ppm for toluene vapor.

Two distinct mechanisms upon absorption of volatile organic compounds into siloxane polymers.

The response of polysiloxane materials to volatile organic compounds (VOCs) including benzene, toluene, ethylbenzene, and toluene (BTEX), as well as cyclohexane, acetone, methanol and isopropanol is studied using thin film large-angle refractometry. Refractive index and thickness changes are measured to quantify the diffusion rate and partition coefficients associated with the absorption and desorption of VOC vapours into polydimethylsiloxane (PDMS) and polydiphenylsiloxane (PDPS) - PDMS copolymer films. Absorption of volatile solvent vapours into siloxane polymers is found to follow two distinct mechanisms with different absorption rates. These mechanisms are also associated with different excess volumes of mixing and may be accompanied by a polymer restructuring step.

VOCs Air Pollutant Cleaning with Polyacrylonitrile/Fly Ash Nanocomposite Electrospun Nanofibrous Membranes

Volatile organic compounds (VOCs) as an environmental pollution, which have many kinds of chemical structures, and many of them are very toxic. Therefore, controlling and reducing the presence of VOCs has become a hot topic among researchers for many years. In this study, the VOCs adsorption capacity of polyacrylonitrile/fly ash (PAN/FA) nanocomposite electrospun nanofibrous membranes were investigated. The results indicated that the PAN with different contents of FA powder (20%, 40%, 60%, 80%, and 100% compared with PAN by weight) could be spun well by electrospinning. The diameter of the fiber was very fine and its arrangement was irregular. The PAN nanofibrous membrane containing 60 wt% FA powder had the highest VOCs absorption capacity compared with other nanofibrous membranes due to its large specific surface area.

Volatile organic compounds absorption in packed column: theoretical assessment of water, DEHA and PDMS 50 as absorbents

A fixed volume packed column was simulated for the absorption at counter-current of four more or less hydrophobic volatile organic compounds (VOCs) in water and in two heavy organic solvents (PDMS 50, a silicone oil) and DEHA (Bis(2-ethylhexyl) adipate). Reliable values of the mass-transfer coefficients were deduced allowing to calculate the VOCs removal efficiency. Disappointing performances in heavy solvents, lower than 60% for isopropanol and acetone, were computed in a 3m height column and using mild conditions (atmospheric pressure and a liquid-to-gas mass flow rate ratio around 2). However, toluene removal efficiencies higher than 90% were simulated.

Deep eutectic solvents as green absorbents of volatile organic pollutants

Volatile organic compounds are a major source of air pollutants. Absorption is an effective solution to treat polluted air loaded with volatile organic compounds, but most actual absorbents are often toxic and non-biodegradable. Here, we tested eutectic solvent mixtures for the absorption of volatile organic compounds for the first time. The affinity of solvent mixtures for toluene, acetaldehyde and dichloromethane was determined by measuring vapour–liquid partition coefficients and liquid phase absorption capacities. Results show that the vapour–liquid partition coefficients vary, at 30 °C, from close to zero for acetaldehyde in the mixtures choline chloride:urea, choline chloride:glycerol and tetrabutylphosphonium bromide:glycerol to 0.124 for dichloromethane in the choline chloride:urea eutectic mixture. These values are similar or even superior to those published for ionic liquids and organic solvents. Solvents based on choline chloride, a food additive, and urea, can solubilize up to 500 times more volatile organic compounds compare to water. Moreover, deep eutectic solvents are easier to prepare and more biodegradable than ionic liquids, which are also toxic. Deep eutectic solvents are more biodegradable than silicone oils, which are also expensive. Furthermore, in terms of recycling, the absorption capacities of the tested solvents remained unchanged during five absorption–desorption cycles. These findings are patented.

Fabrication of Polyurethane/Rare Earth Nanofiber Composite by Electrospinning and Its VOCs Reduction Characteristics

Volatile organic compounds (VOCs) are a source of air pollution and are harmful to both human health and the environment. In this study, we fabricated polyurethane/rare earth (PU/RE) composite nanofibrous membranes via electrospinning with the aim of removing VOCs from air. The morphological structure of PU/RE nanofibrous mats were investigated using FE-SEM, EDX, and XRD experimental analyses. A certain amount of RE (up to 50 wt% compared to PU pellets) particles could be loaded on/into PU fibers. The PU nanofiber containing 50 wt% RE powder had the smallest fiber diameter of 356 nm; it also showed the highest VOCs absorption capacity compared with other composite membranes, having an absorption capacity about 3 times greater than pure PU nanofibers. In addition, all of the PU/RE nanofibrous membranes readily absorbed styrene the most, followed by xylene, toluene, benzene and chloroform. Therefore, the PU/RE nanofibrous membrane can play an important role in removing VOCs from the air, and its development prospects are impressive because they are emerging materials.

Fabrication of Functional Polyurethane/Rare Earth Nanocomposite Membranes by Electrospinning and Its VOCs Absorption Capacity from Air.

Volatile organic compounds (VOCs) are a source of air pollution and are harmful to both human health and the environment. In this study, we fabricated polyurethane/rare earth (PU/RE) composite nanofibrous membranes via electrospinning with the aim of removing VOCs from air. The morphological structure of PU/RE nanofibrous mats was investigated using field emission scanning electron microscopy (FE-SEM), fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) experimental analyses. A certain amount of RE (up to 50 wt. % compared to PU pellets) nanoparticles (NPs) could be loaded on/into PU fibers. The tensile strength of PU/RE nanofibrous membranes decreased slightly with the increasing RE powder content. The PU nanofiber containing 50 wt. % RE powder had the smallest fiber diameter of 356 nm; it also showed the highest VOC absorption capacity compared with other composite membranes, having an absorption capacity about three times greater than pure PU nanofibers. In addition, all of the PU/RE nanofibrous membranes readily absorbed styrene the most, followed by xylene, toluene, benzene and chloroform. Therefore, the PU/RE nanofibrous membrane can play an important role in removing VOCs from the air, and its development prospects are impressive because they are emerging materials.

Effects of PU/LP Nanofiber Thin Films Composite Produced from Electrospun for Absorption VOCs

This study describes the effects of polyurethane/loess powder (PU/LP) nanofiber thin films composite produced from electrospun for absorption volatile organic compounds (VOCs) from air. Environmental issue has become a focus with improving people's living quality. The VOCs are one of the factors that affect the environmental safety. So, in order to improve the environment and safety for people, many air cleaning techniques have been investigated. One of the methods is nanofiber filtration technology. In this study, the PU nanofiber thin film has been studied that it has the adsorption of VOCs capacity, and LP nanoparticles (NPs) can be used as an additive to load into PU nanofiber thin film by electrospinning. For studying PU/LP nanofiber thin films's absorption of VOCs capacity, 4 samples (0, 10, 30, and 50 wt% LP with respect to PU) were manufactured, respectively. The results show that PU composite mats containing 30 wt% LP NPs has the highest VOCs absorption capacity, and the adsorption capacity for toluene was the highest compared to benzene and chloroform.

Colorimetric gas detection by the varying thickness of a thin film of ultrasmall PTSA-coated TiO2 nanoparticles on a Si substrate.

Colorimetric gas sensing is demonstrated by thin films based on ultrasmall TiO2 nanoparticles (NPs) on Si substrates. The NPs are bound into the film by p-toluenesulfonic acid (PTSA) and the film is made to absorb volatile organic compounds (VOCs). Since the color of the sensing element depends on the interference of reflected light from the surface of the film and from the film/silicon substrate interface, colorimetric detection is possible by the varying thickness of the NP-based film. Indeed, VOC absorption causes significant swelling of the film. Thus, the optical path length is increased, interference wavelengths are shifted and the refractive index of the film is decreased. This causes a change of color of the sensor element visible by the naked eye. The color response is rapid and changes reversibly within seconds of exposure. The sensing element is extremely simple and cheap, and can be fabricated by common coating processes.