Typical Volatile Organic Compounds Research Articles

Self-aspiration sampling design for rapid analyses of volatile organic compounds based on atmospheric pressure chemical ionization/photoionization combined ionization source mass spectrometry.

Development of combined mass spectrometry ionization sources has enabled expansion of the application and scope of mass spectrometry. A novel hybrid ionization system combining vacuum ultraviolet (VUV) and atmospheric pressure chemical ionization (APCI) was constructed. Gaseous samples were self-aspirated into an ionization zone through a capillary by negative pressure, generated by high-speed airflow based on the Venturi effect. Compared with APCI mode alone, the signal-to-noise ratio (S/N) in APCI/VUV mode was increased by about 276-times. To increase the ionization efficiency further, correlated experimental conditions were optimized. Four types of volatile organic compounds (VOCs) were tested to evaluate the performance of the APCI/VUV ion source. Excellent linearity and limit of detection were achieved for compounds in mixed solutions. Quantitative analyses of four VOCs (toluene, cyclohexanone, styrene and ethylbenzene) using APCI/VUV-MS were done, and the relative standard deviations (RSDs) were 1.57%, 6.30%, 4.49% and 8.21%, respectively, indicating that the APCI/VUV ionization source had excellent reproducibility. Our results demonstrated that the developed method was promising for analyzing VOCs as well as being rapid, simple, and easy to operate.

Qualitative and quantitative rapid detection of VOCs differentially released by VAP-associated bacteria using PTR-MS and FGC-PTR-MS.

Ventilator-associated pneumonia (VAP) is a prevalent disease caused by microbial infection, resulting in significant morbidity and mortality within the intensive care unit (ICU). The rapid and accurate identification of pathogenic bacteria causing VAP can assist clinicians in formulating timely treatment plans. In this study, we attempted to differentiate bacterial species in VAP by utilizing the volatile organic compounds (VOCs) released by pathogens. We cultured 6 common bacteria in VAP in vitro, including Acinetobacter baumannii, Enterobacter cloacae, Escherichia coli, Pseudomonas aeruginosa, Stenotrophomonas maltophilia, and Staphylococcus aureus, which covered most cases of VAP infection in clinic. After the VOCs released by bacteria were collected in sampling bags, they were quantitatively detected by a proton transfer reaction-mass spectrometry (PTR-MS), and the characteristic ions were qualitatively analyzed through a fast gas chromatography-proton transfer reaction-mass spectrometry (FGC-PTR-MS). After conducting principal component analysis (PCA) and analysis of similarities (ANOSIM), we discovered that the VOCs released by 6 bacteria exhibited differentiation following 3 h of quantitative cultivation in vitro. Additionally, we further investigated the variations in the types and concentrations of bacterial VOCs. The results showed that by utilizing the differences in types of VOCs, 6 bacteria could be classified into 5 sets, except for A. baumannii and E. cloacae which were indistinguishable. Furthermore, we observed significant variations in the concentration ratio of acetaldehyde and methyl mercaptan released by A. baumannii and E. cloacae. In conclusion, the VOCs released by bacteria could effectively differentiate the 6 pathogens commonly associated with VAP, which was expected to assist doctors in formulating treatment plans in time and improve the survival rate of patients.

Primer Design of Volatile Synthesis Coding Genes in Ralstonia syzygii subsp. celebesensis

Microbes produce various types of volatile organic compounds (VOCs) through metabolism, which can be used for diagnostic purposes. Microbes' types and classes of VOCs are very wide, including fatty acid derivatives (hydrocarbons, alcohols, and ketones), aromatic compounds, nitrogen-containing compounds, and volatile sulfur compounds. Microbial volatile organic compounds (VOCs) can also be divided into several chemical classes: alkenes, alcohols, ketones, benzos, pyrazines, sulfides, acids, esters, and terpenes. This study aimed to design primers for genes encoding volatile synthesis in Ralstonia syzygii subsp. celebesensis, which causes blood disease in the banana plant. Some of the genes involved are adc (acetone synthesis), adhP (ethanol synthesis), ilvA, nirBD (ammonia synthesis), mdcA (propionic acid synthesis), cysI (hydrogen sulfide synthesis), and speBC (putrescine synthesis). Primers were designed and examined for specificity in silico using Primer3Plus, Geneious Prime, and BLAST programs. The numbers of nine pairs designed primers were successfully amplifying the related nine VOC genes of R. syzygii subsp. celebesensis for qPCR.

Preparation of CPVC-based activated carbon spheres and insight into the adsorption-desorption performance for typical volatile organic compounds

Chlorinated polyvinyl chloride (CPVC)-based activated carbon spheres with smooth surfaces, good sphericity, interconnected hierarchical porous structure and high porosity have been synthesized by non-solvent induced phase separation method, followed by successive treatments of stabilization, carbonization at 450 °C in N2 atmosphere, and activation with CO2 as an agent at 900–1000 °C. The effect of activation temperatures on the textural properties of activated carbon spheres and their adsorption potential for volatile organic compounds (VOCs) under dynamic conditions is investigated. CO2 activation improves the hierarchy in the microporous range by stimulating the formation of supermicropores and significantly expands the specific surface area and pore volume of activated carbon spheres. The textural properties of adsorbents play a vital role in the adsorption performance of different VOCs. The adsorption capacity of VOC molecules can be greatly promoted by elevating specific surface area and pore volume. Due to the compatibility difference between the VOC molecules and the pore structure of adsorbents, the adsorption capacity follows the order of toluene > m-xylene > n-hexane. The adsorption isotherm of toluene on CPVC-AC1000 can be generally expressed by the Langmuir model. The adsorbents with larger average pore diameters possess a lower activation energy of desorption, which is beneficial for desorption. The carbon sphere activated at 1000 °C is a high-performance adsorbent with good reusability. Thus, the present study provides a synthesis process to produce the activated carbon spheres with high porosity from low-cost CPVC for its application in VOC adsorption.

Study on the effect of different aldehyde modifiers on the fume suppression effect, mechanism and road performance of SBS modified asphalt

In order to curb asphalt fume emissions during the heating process of styrene-butadiene-styrene (SBS) asphalt, three aldehyde modifiers [vanillin (X), citral (N) and amyl cinnamaldehyde (J)] were blended into SBS-modified asphalt to prepare aldehyde-modified asphalt in this paper. By collecting solid particles and volatile organic compounds (VOCs) in asphalt fumes to conduct relevant experiments, we have analyzed the fume suppression effect and suppression mechanism of aldehyde modified asphalt, and finally examined the road performance of aldehyde modifiers with the best fume suppression effect. It was found that the average VOCs concentration of aldehyde modified asphalt was reduced by about 78 % after 30 min. Aldehyde modifiers significantly reduce the compositional type and content of VOCs in SBS asphalt and reduce the risk of carcinogenicity by curbing the emission of substances such as benzene and phenol. J asphalt reduced solid particle emissions from SBS asphalt fume by 31.4 % and outperformed both X and N asphalt in inhibiting the escape of solid particulate matter and carcinogens from asphalt fume. Polymer networks and the cross-linking of chemical molecules are the main reasons for inhibiting the escape of asphalt fume molecules. In addition, the J modifier enhanced the high-temperature stabilization and water-stability properties of asphalt mixtures, but slightly reduced the low-temperature cracking resistance. The results showed that the three aldehyde modifiers were effective in inhibiting the volatilization of fumes from SBS modified asphalt. Among them, with the best effect of curbing fume emissions and a better road performance, J-modified asphalt is promising for the application in asphalt fume prevention and emissions reduction, and provides a new solution to reduce construction pollution and physical harm caused by asphalt fume in the construction process.

Comprehensive Qualitative and Quantitative Colorimetric Sensing of Volatile Organic Compounds Using Monolayered Metal-Organic Framework Films.

Cross-responsive chemical sensors are in high demand owing to their ability to distinguish a broad range of analytes. In this study, a vapochromic sensor array based on metal-organic frameworks (MOFs), which exhibits distinct patterns when exposed to volatile organic compounds (VOCs) and humidity, is developed. Conventional sensor arrays consist of various receptors that produce different responses. The vapochromic MOF-based sensor comprises dicopper paddlewheel clusters and dimethylamine azobenzene as binary colorimetric sensing moieties. Upon exposure to VOCs, the constructed sensor encompasses a broad spectrum of colors, ranging from green to red. Furthermore, the color of the MOF is influenced by the solvent used during the pretreatment. Consequently, monolayered MOF thin films can be adapted to multicomponent array systems by immersing the MOF in different solvents. This system provides both qualitative and quantitative sensing, generating unique color patterns corresponding to specific VOC types. Notably, the sensor successfully discriminates each of 14 common VOCs and water and accurately categorizes unknown samples. Moreover, the system undergoes reversible color changes in response to humidity, obviating the need for high-temperature regeneration steps. This novel approach offers insights into the versatile applications of MOFs by creating a colorimetric sensor array capable of detecting various analytes.

Differentiation analysis of VOCs in Kunming during rainy and dry seasons based on monitoring high temporal resolution

Volatile Organic Compounds (VOCs) play a pivotal role as precursors for O3 formation. 66 VOCs species in Kunming were observed for two consecutive years using an online monitoring system. Concentration characteristics of VOCs, ozone formation potential (OFP), sources and health risks in rainy and dry seasons were investigated. Our results showed that the concentrations of VOCs exhibited significant seasonal differences, with average concentrations of 31.43 ± 17.62 μg/m3 and 64.78 ± 36.38 μg/m3 in the rainy and dry seasons, respectively. Alkanes (16.83 ± 16.75 μg/m3) dominated the VOCs types throughout the monitoring period, followed by halogenated hydrocarbons (13.38 ± 16.20 μg/m3), olefins (10.77 ± 14.34 μg/m3), aromatics (6.64 ± 6.71 μg/m3), and alkynes (0.36 ± 0.37 μg/m3). The OFP values in rainy and dry seasons were 86.10 μg/m3 and 198.55 μg/m3, respectively. The most substantial contribution to OFP originated from olefins, which could be associated with crude oil refining activities around Kunming. Vehicles and petrochemicals were the main sources in Kunming based on PMF calculations. Biomass burning (10.63%) and biogenic emission (8.68%) were noted in dry and rainy seasons, respectively. HYSPLIT analysis established that Kunming's air quality was significantly affected by the southwestward air mass transmission, particularly through a large industrial park. In the dry season, Kunming is significantly more affected by air mass transport from this direction than in the rainy season. The carcinogenic risk of benzene was high as 10 × 10−6 and 2.4 × 10−6 in the rainy and dry seasons, respectively. In conclusion, Kunming's VOCs control measures should pay more attention to the influence of the upwind industrial park.

Associations between inhalation of typical volatile and semi-volatile organic compounds in e-waste dismantling workers with liver function damage

Studies in cell culture and animal models suggest hepatotoxicity of some volatile organic compounds (VOCs) and semi-volatile organic compounds (SVOCs), however, their effects in human populations under real exposure conditions have never been clarified. In this cross-sectional study, 224 participants, 38 e-waste dismantling workers and 186 subjects residing near to the dismantling sites in southern China, were evaluated for personal inhalational exposure to 72 VOCs and 91 SVOCs according to site-specific atmospheric chemical concentrations and personal exposure time. Additionally, their serum samples were subjected to liver function tests (LFTs), including total protein (TP), albumin (ALB), globulin (GLB), aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma-glutamyl transpeptidase (GGT), and bilirubin. Linear regression analysis of the VOC/SVOC levels against the LFTs results indicated that VOC exposure was negatively associated with the TP, ALB, GLB levels (indicating liver-specific protein synthesis functions), while positively associated with AST, ALT, GGT activities (marking liver damage). Somehow, SVOC exposure appeared to be positively associated with not only AST and ALT but also TP and ALB. These findings were supported by the quantile g-computation analysis and confirmed in the Bayesian kernel machine regression model. This study indicates that simultaneous inhalation of VOCs and SVOCs may impair human liver functions.

Micro-heater embedded Ni-SnO2 ordered nanoporous films: On-chip fabrication for fast, sensitive, and selective gas sensing towards multiple VOCs for air quality monitoring

The ability to simultaneously detect multiple volatile organic compounds (VOCs) is crucial for assessing indoor air quality and addressing significant health hazards. In this study, we present a sacrificial template approach for on-chip fabrication of two-dimensional (2D) Ni-doped SnO2 nanoporous sensing films on micro-heater substrates. The technical analysis shows that the resulting honeycomb-like ultrathin Ni-SnO2 sensing layer on a suspended substrate maintains perfect structural integrity and consistency. The Ni-SnO2 sensors exhibit exceptional characteristics, including a ppb-level detection limit, high sensitivity, fast response/recovery time, and signal repeatability for typical VOCs, while operating at a low power consumption of 25 mW. Additionally, the Ni-doping enhances the sensors' cross-sensitivity to various forms of VOCs, while causing a discernible response inhibition towards flammable or exhaust gases. Furthermore, X-ray photoelectron spectroscopy (XPS) and in-situ Raman spectra reveal a Ni2+-substitution induced surface adsorbed oxygen species enrichment mechanism for sensing enhancement. Thus, the developed Ni-SnO2 sensors hold promise as future candidates for reliable air quality assessment by real-time monitoring of overall concentrations of multiple VOCs.

Effect of temperature on VOC emissions and odor from vehicle carpet

Volatile organic compounds (VOCs) released from carpets deteriorate the air quality in the confined vehicle interior. The wide range of temperatures experienced by vehicle carpets impacts VOC and odor emissions, affecting the physical and mental health of occupants. We investigated the VOC emissions and odor characteristics of vehicle carpets at 25, 40, 50, and 60 °C, respectively. An approach was developed for simultaneous objective sampling and subjective evaluation in a 1 m3 chamber with controlled temperature, humidity, and ventilation. Sensory panelists were screened and trained to evaluate the odor intensity, preference, and type. The emitted VOC types and concentrations increased with temperature; there were 4.5 times more VOC types at 60 °C than at 25 °C. The emission of aromatic compounds, heterocyclic compounds, acids, esters, and ketones significantly increased with temperature. The interaction between odorants affected odor characteristics at the four temperatures; the dominant odors were plastic-like and stinky at 25 °C, rubber- and leather-like at 40 and 50 °C, and aroma at 60 °C. Further quantitative and qualitative exploration of substances, odors, and health effects from carpet emissions at different temperatures could help improve the vehicle environment.

Fly ash-based zeolitic materials of different surface chemistry and texture: Insight into adsorption performance and mechanisms of aqueous BTEX removal

Water contamination caused by anthropogenic, and unforecasted release of BTEX (benzene, toluene, ethylbenzene and xylene) compounds threatens the quality and integrity of aquatic ecosystems. BTEX sorption with novel materials characterized by increased hydrophobicity and stability has been proposed to overcome such contamination. This study aimed to investigate the whole array of hydrothermally synthesized zeolitic materials exhibiting different properties, as well as zeolite/carbon and zeolite/vermiculite composites, to analyse their potential in removing aqueous BTEX. Various parameters and experimental conditions, including the type of volatile organic compounds (VOCs), initial concentration, BTEX coexistence, and increased solution salinity, were studied to verify the applicability of the derived materials. The adsorption capacity of the materials and their governing removal mechanisms were additionally elucidated. The primary removal mechanism involved partitioning on unburned carbon residues, which was observed in zeolite/carbon composites showing the highest BTEX removal efficiency. NaA-zeolite/carbon composite was the most effective in removal of BTEX, with the removal capacity of 15.36 mg/g towards p-xylene. Moreover, the increased salinity of the BTEX solution affects adsorption performance for polar adsorbates, irrespectively of the applied zeolite/carbon composite. Fly-ash (FA) and high-carbon fly-ash (HCFA) were successfully valorised into products with better textural features. These products may effectively tackle organic water pollution caused by VOCs under near-real-life conditions.

Ultrathin MnO2 with strong lattice disorder for catalytic oxidation of volatile organic compounds

Catalytic oxidation proves the most promising technology for volatile organic compounds (VOCs) abatement. Lattice disorder plays a crucial role in the catalytic activity of catalysts due to the exposure of more active sites. Inspired by this, we successfully prepared a series of ε-MnO2 with different lattice disorder defects via several simple methods and applied them to the catalytic oxidation of two typical VOCs (toluene and acetone). Various characterizations and performance tests confirm that the ultrathin (1.4–1.8 nm) structure and strong lattice disorder can enhance the low temperature reduction and reactive oxygen species, so that MnO2-R exhibits excellent toluene and acetone oxidation activities. In-situ DRIFTS tests were carried out to detect reaction intermediates in the toluene and acetone oxidation process on the catalyst surface. Moreover, we propose a possible synergistic mechanism for toluene and acetone mixtures catalytic oxidation. This work reveals the important role of lattice disorder defects in the catalytic oxidation of VOCs on Mn-based catalysts, and deepens the insights of the reaction path in toluene and acetone catalytic oxidation.

Efficient capture of benzene and its homologues volatile organic compounds with protic [MIM][NTF2] and aprotic [EMIM][NTF2] ionic liquids: Experimental and computational thermodynamics

Using new green solvents to effectively capture volatile organic compounds (VOCs) is considered as an attractive green sustainable chemical development route. In this work, benzene, toluene, ethylbenzene and p-xylene (BTEX) were selected as typical aromatic VOCs. The gas absorption performance of proton [MIM][NTF2] and aprotic [EMIM][NTF2] ionic liquids (ILs) for BTEX were studied by computational thermodynamics combined with gas absorption experiments. Absorption experiments of BTEX and regeneration experiments of ILs were carried out at different temperatures, and ILs had good stability. The interaction type and intensity were determined by Interaction Region Indicator (IRI) analysis of IL-BTEX blend systems. The C-H···π and π-π interaction between imidazole ring and BTEX were the direct reason why ILs can efficiently absorb BTEX. Molecular dynamics simulations were performed to explore the diffusion behavior of gas in ILs. The increase of methyl group increases the interaction strength of the system, and the fractional free volume of IL-BTEX blend systems decreases gradually, which limits the diffusion of BTEX. Non-bond interaction analysis shows that van der Waals interaction was the main driving force of BTEX absorption in ILs.

Microbial metabolism and health risk assessment of kitchen waste odor VOCs.

Kitchen waste (KW) generates odors comprising complex volatile organic compounds (VOCs). We used gas chromatography-mass spectrometry to analyze VOCs, and 16S gene sequencing was used to analyze the microbial community composition and microbial metabolic mechanism. The results showed that the major odor-causing VOCs were hydrogen sulfide, methanethiol, methyl sulfide, dimethyl disulfide, and ethyl acetate. As the temperature increased, the VOCs and microbial community composition became more complex, and the microbial community related to VOC production included Leuconostoc, Pediococcus, Acetobacter, and Weissella. Based on PICRUSt2 analysis, the possibility of typical VOC interconversion by microbial metabolism was low. It was more likely that precursor substances were catalyzed by enzymes to generate the corresponding VOCs. Attention should be given to trichloromethane and 1,2-dichloroethane, which may cause adverse health effects through long-term inhalation. The study results provide guidance for controlling VOCs from KW.

Self-assembly of MOFs-like materials by Zn2+ and histidine functionalized graphene quantum dots for the efficient removal of VOCs simulants

Volatile organic compounds (VOCs) in the field of printing and packaging, have caused great harm to the environment. Therefore, the removal of volatile organic compounds (VOCs) is a hot topic, and metal-organic frameworks (MOFs) and graphene quantum dots (GQDs) have been applied in this field. However, improving the removal efficiency of different VOCs by using the two kinds of materials is still a great challenge. Herein, ZIF-8 like materials of Zn-His-GQDs were prepared by assembling Zn2+ and histidine functionalized GQDs (His-GQDs) in this work. The morphologies, structure and adsorption performances of Zn-His-GQDs were investigated. These results showed that mesoporous Zn-His-GQDs with a specific surface area of 63.3 m2·g−1 had similar structure to ZIF-8. When the content of Zn-His-GQDs was 200 mg, the equilibrium adsorption capacity for toluene solution of 500 mg·L−1 and ethyl acetate solution of 1600 mg·L−1 was 350 mg·L−1 and 669.44 mg·L−1, respectively. Due to channel filling, cation-π interaction, π-π interaction, hydrogen bond and high surface energy, Zn-His-GQDs exhibited a relative high removal efficiency for high concentration of toluene and ethyl acetate. The removal rate of Zn-His-GQDs on toluene and ethyl acetate after five cycles remained 59.80 % and 36.75 %, respectively. Moreover, this kind of MOFs like materials maintained stable structure during the adsorption in different pH solutions. Therefore, as-prepared Zn-His-GQDs with excellent adsorption performances for typical VOCs simulants in this work have potential application in the treatment of VOCs in the field of printing and packaging.

The smell of death. State-of-the-art and future research directions.

The decomposition of a body is inseparably associated with the release of several types of odors. This phenomenon has been used in the training of sniffer dogs for decades. The odor profile associated with decomposition consists of a range of volatile organic compounds (VOCs), chemical composition of which varies over time, temperature, environmental conditions, and the type of microorganisms, and insects colonizing the carcass. Mercaptans are responsible for the bad smell associated with corpses; however, there are no unified recommendations for conducting forensic analysis based on the detectable odor of revealed corpses and previous research on VOCs shows differing results. The aim of this review is to systematize the current knowledge on the type of volatile organic compounds related to the decomposition process, depending on a few variables. This knowledge will improve the methods of VOCs detection and analysis to be used in modern forensic diagnostics and improve the methods of training dogs for forensic applications.

Catalytic degradation of benzene at room temperature over FeN4O2 sites embedded in porous carbon

Benzene and its aromatic derivatives are typical volatile organic compounds for indoor and outdoor air pollution, harmful to human health and the environment. It has been considered extremely difficult to break down benzene rings at ambient conditions without external energy input, due to the extraordinary stability of the aromatic structure. Here, we show one such solution that can thoroughly degrade benzene to basically water and carbon dioxide at 25 °C in air using atomically dispersed Fe in N-doped porous carbon, with almost 100% benzene conversion. Further experimental studies combined with molecular simulations reveal the mechanism of this catalytic reaction. Hydroxyl radicals (·OH) evolved on the atomically dispersed FeN4O2 catalytic centers were found responsible for initiating and completing the oxidation of benzene. This work provides a new chemistry to degrade aromatics at ambient conditions and also a pathway to generate active ·OH oxidant for generic remediation of organic pollutants.

Recycling Graphite from Spent Lithium Batteries for Efficient Solar-Driven Interfacial Evaporation to Obtain Clean Water.

Solar-driven interfacial evaporation technology is regarded as an attracting sustainable strategy for obtaining portable water from seawater and wastewater, and the recycle of waste materials to fabricate efficient photothermal materials as evaporator to efficiently utilize solar energy is very critical, but still difficult. To this purpose, graphite recovered from spent lithium-ion batteries (SLIBs) was realized using a simple acid leaching method, and a reconstructed graphite-based porous hydrogel (RG-PH) was subsequently fabricated by crosslinking foaming method. The incorporation of reconstructed graphite (RG) improves the mechanical characteristics of hydrogels and the light absorption performance significantly. The evaporation rate of optimized RG-PH can constantly reach 3.4278 kg m-2 h-1 for desalination under a one solar irradiation, and it also showed the excellent salt resistance in various salty water. Moreover, RG-PH has a strong elimination of a variety of organic contaminants in wastewater, including the typical volatile organic compound of phenol. This research shows the potential application of flexible and durable solar evaporators made from waste materials in purifying seawater and wastewater, not only contributing to carbon neutrality by recycling graphite from SLIBs, but also ensuring the cost-effectiveness harvest of solar energy for constantly obtaining clean water.

A DFT Study of Volatile Organic Compounds Detection on Pristine and Pt-Decorated SnS Monolayers.

Real-time monitoring of volatile organic compounds (VOCs) is crucial for both industrial production and daily life. However, the non-reactive nature of VOCs and their low concentrations pose a significant challenge for developing sensors. In this study, we investigated the adsorption behaviors of typical VOCs (C2H4, C2H6, and C6H6), on pristine and Pt-decorated SnS monolayers using density functional theory (DFT) calculations. Pristine SnS monolayers have limited charge transfer and long adsorption distances to VOC molecules, resulting in VOC insensitivity. The introduction of Pt atoms promotes charge transfer, creates new energy levels, and increases the overlap of the density of states, thereby enhancing electron excitation and improving gas sensitivity. Pt-decorated SnS monolayers exhibited high sensitivities of 241,921.7%, 35.7%, and 74.3% towards C2H4, C2H6, and C6H6, respectively. These values are 142,306.9, 23.8, and 82.6 times higher than those of pristine SnS monolayers, respectively. Moreover, the moderate adsorption energies of adsorbing C2H6 and C6H6 molecules ensure that Pt-decorated SnS monolayers possess good reversibility with a short recovery time at 298 K. When heated to 498 K, C2H4 molecules desorbs from the surface of Pt-decorated SnS monolayer in 162.33 s. Our results indicate that Pt-decorated SnS monolayers could be superior candidates for sensing VOCs with high selectivity, sensitivity, and reversibility.

Species-Selective Detection of Volatile Organic Compounds by Ionic Liquid-Based Electrolyte Using Electrochemical Methods.

The detection of volatile organic compounds (VOCs) is an important topic for environmental safety and public health. However, the current commercial VOC detectors suffer from cross-sensitivity and low reproducibility. In this work, we present species-selective detection for VOCs using an electrochemical cell based on ionic liquid (IL) electrolytes with features of high selectivity and reliability. The voltammograms measured with the IL-based electrolyte absorbing different VOCs exhibited species-selective features that were extracted and classified by linear discriminant analysis (LDA). The detection system could identify as many as four types of VOCs, including methanol, ethanol, acetone, formaldehyde, and additional water. A mixture of methanol and formaldehyde was detected as well. The sample required for the VOCs classification system was 50 μL, or 1.164 mmol, on average. The response time for each VOC measurement is as fast as 24 s. The volume of VOCs such as formaldehyde in solution could also be quantified by LDA and electrochemical impedance spectroscopy techniques, respectively. The system showed a tunable detection range for 1.6 and 16% (w/v) CH2O solution by adjusting the composition of the electrolyte. The limit of detection was as low as 1 μL. For the 1.6% CH2O solution, the linearity calibration range was determined to be from 5.30 to 53.00 μmol with a limit of detection at 0.53 μmol. The mechanisms for VOCs determination and quantification are also thoroughly discussed. It is expected that this work could provide a new insight into the concept of electrochemical detection of VOCs with machine learning analysis and be applied to both VOCs gas monitoring and fluid detection.