Toxic Volatile Organic Compounds Research Articles

Long-term analysis of BTEX concentrations and health risks in semi-arid urban regions

Rajasthan, experiencing rapid industrialization and urbanization, faces critical air quality challenges, particularly concerning toxic volatile organic compounds (VOCs) such as BTEX (Benzene, Toluene, Ethylbenzene, Xylene). This study presents a long-term analysis of BTEX concentrations across various cities in Rajasthan, India, using data from the Central Pollution Control Board (CPCB) from 2017 to 2022. The findings revealed that the average ∑BTEX concentrations increased from 4.15 µg/m3 in 2017 to 12.29 µg/m3 in 2022, with a temporary decline in 2020. The Hazard Quotient (HQ) values for BTEX exposure ranged from 0.052 to 0.15 for males, 0.056 to 0.17 for females, and 0.09 to 0.29 for children over the study period, indicating higher health risks for children. Similarly, the Lifetime Cancer Risk (LCR) values varied from 6.04 × 10⁻⁶ to 1.92 × 10⁻5 for males, 1.09 × 10⁻⁶ to 2.24 × 10⁻5 for females, and 1.17 × 10⁻5 to 3.73 × 10⁻5 for children. The results demonstrate that children are at a greater cancer risk from BTEX exposure compared to adults. This study emphasizes the urgent need for effective air pollution control measures and continuous monitoring to protect public health, particularly vulnerable populations like children.

Fuel fumes and foliage: the fate of speciated gasoline VOCs during phytoremediation and their impact on the bacterial phenotype

The capacity of indoor plants including green walls to capture, deposit and remediate individual volatile organic compounds (VOCs) has been well documented. However, in realistic settings, plant systems are exposed to a complex mixture of VOCs from highly varied various emission sources. Gasoline vapour is one of the major sources of these emissions, containing high concentrations of the carcinogens benzene, toluene, ethylbenzene and xylene (BTEX). Using both solid phase micro extraction (SPME) and quick, easy, cheap, effective, rugged and safe (QuEChERS) sampling techniques, we assessed the dynamics of individual speciated gasoline VOC phytoremediation from the air and uptake within green wall plant species and growth substrates within a small passive green wall system, along with quantifying the phenotypic changes within the plant-associated bacterial communities resulting from gasoline exposure. Over 8 hours the green wall system achieved 100% removal of atmospheric benzene, 1,2,3-trimethyl, eicosane and hexadecane, benzene 1,3-diethyl-; 1,3,5 cycloheptatriene,7- ethyl and carbonic acid eicosyl vinyl ester. All plant species tested demonstrated the accumulation 45 petrochemical VOCs (pVOCs) with Spathiphyllum wallisii successfully accumulating the majority of pVOC functional groups after 24 h of gasoline exposure. Within the plants phyllospheric bacterial communities, changes in both cellular complexity and granularity appeared to increase as a result of gasoline exposure, while cell size diminished. This work provides novel findings on the VOC removal processes of botanical systems for realistic and highly toxic VOC profiles.

A New Look at Diffusion in Vapor Intrusion Assessments; Passive Adsorptive Diffusion Samplers

AbstractVapor intrusion of toxic volatile organic compounds (VOCs) from subsurface soil vapor, through a building slab/floor, and into the indoor air is an important environmental contaminant transport mechanism. It is widely believed that advective flow, driven by the pressure differential between the subslab and indoor air, is the primary mechanism of subslab soil vapor entry into buildings. This paper explores the hypothesis that molecular diffusion through the slab may potentially play a larger role in vapor intrusion than previously believed and may even be the predominant vapor intrusion mechanism when the subslab vapor source strength is sufficiently high or the pressure differential is relatively low. A novel sampling device, referred to as a Passive Adsorptive Diffusion Sampler (PADS), is presented for the purpose of directly measuring the diffusion of VOCs through a building slab. A vacant warehouse was identified as a case study site where historical sampling had determined that vapor intrusion of trichloroethene (TCE) was adversely impacting the indoor air. Calculations using Fick's First Law of Diffusion are presented which demonstrate that diffusion alone can theoretically account for all the TCE observed in the indoor air at this building based on an effective diffusion coefficient for concrete that was calculated from the Johnson and Ettinger Model. Two groups of nine replicate PADS were deployed at two areas on the slab and used to measure the flux and effective diffusion coefficient at each of the 18 total points, which showed an order of magnitude variability within each area and over two orders of magnitude variability overall. These results indicate that diffusion through concrete is inherently variable when measured at a sub‐meter scale. However, when combined over both areas, the overall average approached that calculated from the Johnson and Ettinger Model. An additional 12 PADS were deployed across the building slab (for a total of 30) to quantify the overall building‐wide diffusive flux. This area‐weighted average diffusive flux was consistent with the predicted diffusive flux as calculated from Fick's First Law and the vapor intrusion mass input required to achieve the observed indoor air TCE concentration. The results of this study show that PADS provides a simple way to measure diffusive flux directly without having to drill through the slab. However, significant variability in the measured flux should be expected and will need to be accounted for by the inclusion of a relatively large number of samples including replicates. When using PADs at a new site, the collection of traditional subslab vapors at a select number of locations is recommended for the verification of a building‐specific effective diffusion coefficient, which may not necessarily be the same as for this building.

Assessing and mitigating health risks of workers exposed to volatile organic compounds in contaminated soils during active pit excavation: Accounting for exposure variability and uncertainty

Health risks to workers involved in the active pit excavation of volatile organic compound (VOC)-contaminated soils have been overlooked, despite the prevalence of ex-situ remediation practices in China. This study developed a new VOC exposure in pit excavation (VEPE) model that comprehensively accounts for the release of gas-phase VOCs in soil pores, surface volatilization of newly exposed agglomerates, and volatilization of newly exposed excavation pit bottom surfaces. Additionally, the model incorporates the concentration variation of soil contaminants, spatial heterogeneity of soil properties, and the variability and uncertainty of worker exposure using two-dimensional Monte Carlo simulation (2D MCS), highlighting the importance of controlling area of new exposure surfaces, soil saturation, and air exchange during the pit excavation to mitigate risks. The study evaluated worker-health-based risks during the excavation of a VOC-contaminated site in Beijing and revealed that the inhalation cancer risk for trichloroethylene (2.35 × 10−6) and its hazard quotient (143.92) exceed the acceptable levels (10−6 and 1.0, respectively). The comparison of models demonstrated the theoretical advancements of the VEPE model over existing pit excavation models, while the field test comparison showed a significant improvement in the predication accuracy. This study addresses the under-researched area of worker safety in contaminated excavation sites. The findings have the potential to promote cleaner and more sustainable practices in ex-situ contaminated site remediation by providing valuable insights for implementing effective control measures to mitigate the emission of toxic VOCs, thereby reducing adverse social and environmental impacts.

Rapidly photocatalytic degradation of toluene boosted by plasmonic effect and Schottky junction on Pt nanoparticles engineered self-supporting Cu2O nanowires

Photocatalytic degradation indoor toluene is one of the most environment-compatible strategies for manufacturing advanced air purifiers. A novel self-supporting photocatalysts, Pt/Cu2O nanowires growing from Cu mesh were constructed using energy-saving methods. The 5 nm Pt nanoparticles are well dispersed on Cu2O, establishing intimate Pt/Cu2O Schottky junction that curtails electron-hole recombination. Additionally, Pt nanoparticles contribute a plasmonic heating effect and an oscillating electric field for accelerating the photocatalytic rates and enhancing overall catalytic activity. By virtue of the Pt/Cu2O Schottky junction and plasmonic effect of the Pt nanoparticles, toluene is efficiently mineralized into CO2 and H2O. The optimal Pt/Cu2O catalyst achieve a toluene elimination rate of 93.65%, with the mineralization degree high up to 92.23%. This study confirms the practicability of the self-supporting Pt/Cu2O catalyst, which figures out new ideas for designing high-performance photocatalyst for removing typical and toxic volatile organic compounds.

Diethylbenzene and ethyltoluene adsorption studies on novel beta antimonide phosphorus nanosheets-a first-principle study.

In the present work, we examined the sensing behavior of monolayer beta antimonide phosphorus (β-SbP) sheets towards toxic volatile organic compounds (VOCs) namely, 1,2-diethylbenzene and 2-ethyltoluene using density functional theory (DFT) method. At first, using cohesive energy structural stability of the monolayer β-SbP is confirmed. The calculated energy band gap value of monolayer β-SbP is 2.168eV, which is a semiconductor. Furthermore, the adsorption properties of 1,2-diethylbenzene and 2-ethyltoluene on β-SbP are studied through key factors, such as adsorption energy, Mulliken charge transfer, and relative band gap variation. The adsorption energy clearly shows (- 0.335 to - 0.903eV) that both 1,2-diethylbenzene and 2-ethyltoluene are physisorbed on β-SbP monolayer. Besides, Mulliken charge transfer falls in the range of - 0.465 to 0.933 e; this information clearly shows that the β-SbP monolayer is a potential candidate for sensing 1,2-diethylbenzene and 2-ethyltoluene molecules. The structural firmness including electronic and adsorption properties of 1,2-diethylbenzene and 2-ethyltoluene on β-SbP monolayer are investigated with the support of the DFT method. Particularly, the hybrid generalized gradient approximation (hybrid GGA) along with Beck's three-parameter + Lee-Yang-Parr (B3LYP) exchange-correlation functional is utilized for relaxing the β-SbP monolayer. In the present work, all calculations are performed using the Quantum Atomistic Tool Kit (ATK) simulation package. In the present work, we utilized β-SbP monolayer as a chief sensing element to detect 1,2-diethylbenzene and 2-ethyltoluene to safeguard humans from toxic environments.

Evaluation of the novel endophytic fungus Chaetomium ascotrichoides 1-24-2 from Pinus massoniana as a biocontrol agent against pine wilt disease caused by Bursaphelenchus xylophilus.

Bursaphelenchus xylophilus, the causative agent of pine wilt disease (PWD), is an ever-increasing threat to Pinus forests worldwide. This study aimed to develop biological control of PWD by the application of endophytic fungi isolated from healthy pine trees. We successfully isolated a novel endophytic fungal strain 1-24-2 from branches of healthy Pinus massoniana. The culture filtrates (CFs) of strain 1-24-2 exhibited strong nematicidal activity against Bursaphelenchus xylophilus, with a corrected mortality rate of 99.00%. Based on the morphological and molecular characteristics, the isolated strain 1-24-2 was identified as Chaetomium ascotrichoides. In the in-planta assay, pine seedlings (2-years-old) treated with 1-24-2 CFs + pine wood nematode (T2) showed a significant control effect of 80%. A total of 24 toxic compounds were first identified from 1-24-2 CFs through gas chromatography-mass spectrometry (GC-MS) analysis, from which O-methylisourea, 2-chlorobenzothiazole, and 4,5,6-trihydroxy-7-methylphthalide showed robust binding sites at Tyr119 against phosphoethanolamine methyltransferase (PMT) protein of Bursaphelenchus xylophilus by molecular docking approach and could be used as potential compounds for developing effective nematicides. Interestingly, strain 1-24-2 produces toxic volatile organic compounds (VOCs), which disturb the natural development process of B. xylophilus, whose total number decreased by up to 83.32% in the treatment group as compared to control and also reduced Botrytis cinerea growth by up to 71.01%. Our results highlight the potential of C. ascotrichoides 1-24-2 as a promising biocontrol agent with solid nematicidal activity against B. xylophilus. This is the first report of C. ascotrichoides isolated from P. massoniana exhibiting strong biocontrol potential against B. xylophilus in the world. © 2024 Society of Chemical Industry.

Current Concepts towards the Health Hazards of BBQ Smoke and Newer Possibilities for Risk Mitigation: A Pilot Study

The toxic and unhealthy effects of Barbecue (BBQ) smoke is well known. Incomplete combustion of energy sources such as charcoal and wood chips give rise to Volatile Organic Compounds (VOCs) such as toluene and formaldehyde. They also give rise to particulate matter of small caliber e.g. PM25 that readily enter the pulmonary system. The net effect is a substantial risk of pulmonary diseases and possible carcinogenic effects. However, little progress has been made in terms of finding a way to cleanse the smoke of these potential hazards while at the same time preserving the ingredients of BBQ that prompt its use in the first place. Syringol and Guaiacol are two VOCs that provide the desirable smell and taste for the BBQ user. Here we review the progress to date of the steps that have been taken to solve this health concern and then propose a novel plan to execute differential scrubbing of BBQ smoke. It is suggested that activated carbon will preferentially adsorb more of the main body of VOCs than Syringol and Guaiacol simply because the latter two compounds are phenols which happen to be polar molecules. Activated carbon used for scrubbers is non-polar and tends to adsorb non-polar VOCs rather than polar VOCs. A pilot experiment was performed to exhibit the predicted differential adsorption. Smoke generated from an ordinary BBQ grill was allowed to be scrubbed by a high concentration that removed all VOCs including Syringol. The Syringol was monitored indirectly by an olfaction test. A 50% reduction in carbon concentration resulted in a dramatic differential reduction of the VOCs with a much greater adsorption of overall VOCs in comparison to Syringol. The results are encouraging in that this differential adsorption process does provide a potential to rid much of the toxic VOCs from common BBQ practice. Future studies are suggested including the design of a carbon scrubber system for the common BBQ grill.

Emission of volatile organic compounds during open fire cooking with wood biomass: Traditional three-stone open fire vs. gasifier cooking stove in rural Kenya

Cooking with wood biomass fuels releases hazardous air pollutants, including volatile organic compounds (VOCs), that often disproportionally affect women and children. This study, conducted in Kwale and Siaya counties in Kenya, employed thermal desorption gas chromatography – mass spectrometry to analyse VOC emissions from cooking with a wood biomass three-stone open fire vs. top-lit updraft gasifier stove. In kitchens with adequate ventilation, total VOC levels increased from 35–252 μg∙m−3 before cooking to 2235–5371 μg∙m−3 during open fire cooking, whereas use of a gasifier stove resulted in reduced emissions from cooking by 48–77 % (506–2778 μg∙m−3). However, in kitchens with poor ventilation, there was only a moderate difference in total VOC levels between the two methods of cooking (9034–9378 μg∙m−3 vs. 6727–8201 μg∙m−3 for the three-stone open fire vs. gasifier stove, respectively). Using a non-target screening approach revealed significantly increased levels of VOCs, particularly benzenoids, oxygenated and heterocyclic compounds, when cooking with the traditional open fire, especially in closed kitchens, highlighting the effects of poor ventilation. Key hazardous VOCs included benzene, naphthalene, phenols and furans, suggesting potential health risks from cooking. In kitchens with good ventilation, use of the gasifier stove markedly reduced emissions of these priority toxic VOCs compared to cooking with an open fire. Thus, substituting open fires with gasifier stoves could help to improve household air quality and alleviate health risks. The study revealed that VOCs were present prior to cooking, possibly originating from previously cooked food (buildup) or the outside environment. VOC emissions were also exacerbated by reduced air flow in high humidity during rainfall, suggesting an area for further research. The findings underscore the importance of adopting cleaner cooking technologies and enhancing kitchen ventilation to mitigate the impacts of VOCs in developing countries.

Efficient Catalytic Elimination of Toxic Volatile Organic Compounds via Advanced Oxidation Process Wet Scrubbing with Bifunctional Cobalt Sulfide/Activated Carbon Catalysts.

Advanced oxidation process (AOP) wet scrubber is a powerful and clean technology for organic pollutant treatment but still presents great challenges in removing the highly toxic and hydrophobic volatile organic compounds (VOCs). Herein, we elaborately designed a bifunctional cobalt sulfide (CoS2)/activated carbon (AC) catalyst to activate peroxymonosulfate (PMS) for efficient toxic VOC removal in an AOP wet scrubber. By combining the excellent VOC adsorption capacity of AC with the highly efficient PMS activation activity of CoS2, CoS2/AC can rapidly capture VOCs from the gas phase to proceed with the SO4•- and HO• radical-induced oxidation reaction. More than 90% of aromatic VOCs were removed over a wide pH range (3-11) with low Co ion leaching (0.19 mg/L). The electron-rich sulfur vacancies and low-valence Co species were the main active sites for PMS activation. SO4•- was mainly responsible for the initial oxidation of VOCs, while HO• and O2 acted in the subsequent ring-opening and mineralization processes of intermediates. No gaseous intermediates from VOC oxidation were detected, and the highly toxic liquid intermediates like benzene were also greatly decreased, thus effectively reducing the health toxicity associated with byproduct emissions. This work provided a comprehensive understanding of the deep oxidation of VOCs via AOP wet scrubber, significantly accelerating its application in environmental remediation.

Recent advances in electrostatic precipitation of particles from flue gases generated by domestic heating appliances. A brief outlook

Winter season is the time of increased emission of exhaust gases from household heating appliances containing particulate matter (PM) and other noxious contaminants. Many old buildings and single houses, particularly at rural and small town regions, still use stoves, fireplaces or ovens to flat heating. Besides qualified fuels like coal or biomass pellets, all kinds of wastes are also burned in many cases, producing not only mineral particles but also toxic volatile organic compounds or other carcinogenic species. To solve the problem of high level of emission of solid particles and organic-compound molecules different constructions of electrostatic precipitators, which can remove such particles, have been developed in last two decades, which were designed to operate downstream of small domestic boilers. Such electrostatic precipitator must comply with the ECODESIGN emission limits, which set the emission level at 20 mg/m3, for biomass. The mass collection efficiency should be higher than 95 % to obtain this emission level. This brief review presents different constructions of electrostatic precipitators designed to be used for the removal of fly ash particles from domestic heating appliances.

Recent Advancements in the Utilization of s-Block Organometallic Reagents in Organic Synthesis with Sustainable Solvents.

This mini-review offers a comprehensive overview of the advancements made over the last three years in utilizing highly polar s-block organometallic reagents (specifically, RLi, RNa and RMgX compounds) in organic synthesis run under bench-type reaction conditions. These conditions involve exposure to air/moisture and are carried out at room temperature, with the use of sustainable solvents as reaction media. In the examples provided, the adoption of Deep Eutectic Solvents (DESs) or even water as non-conventional and protic reaction media has not only replicated the traditional chemistry of these organometallic reagents in conventional and toxic volatile organic compounds under Schlenk-type reaction conditions (typically involving low temperatures of -78 °C to 0 °C and a protective atmosphere of N2 or Ar), but has also resulted in higher conversions and selectivities within remarkably short reaction times (measured in s/min). Furthermore, the application of the aforementioned polar organometallics under bench-type reaction conditions (at room temperature/under air) has been extended to other environmentally responsible reaction media, such as more sustainable ethereal solvents (e.g., CPME or 2-MeTHF). Notably, this innovative approach contributes to enhancing the overall sustainability of s-block-metal-mediated organic processes, thereby aligning with several key principles of Green Chemistry.

Highly Stable Self-Cleaning Paints Based on Waste-Valorized PNC-Doped TiO2 Nanoparticles.

Adding photocatalytically active TiO2 nanoparticles (NPs) to polymeric paints is a feasible route toward self-cleaning coatings. While paint modification by TiO2-NPs may improve photoactivity, it may also cause polymer degradation and release of toxic volatile organic compounds. To counterbalance adverse effects, a synthesis method for nonmetal (P, N, and C)-doped TiO2-NPs is introduced, based purely on waste valorization. PNC-doped TiO2-NP characterization by vibrational and photoelectron spectroscopy, electron microscopy, diffraction, and thermal analysis suggests that TiO2-NPs were modified with phosphate (P=O), imine species (R=N-R), and carbon, which also hindered the anatase/rutile phase transformation, even upon 700 °C calcination. When added to water-based paints, PNC-doped TiO2-NPs achieved 96% removal of surface-adsorbed pollutants under natural sunlight or UV, paralleled by stability of the paint formulation, as confirmed by micro-Fourier transform infrared (FTIR) surface analysis. The origin of the photoinduced self-cleaning properties was rationalized by three-dimensional (3D) and synchronous photoluminescence spectroscopy, indicating that the dopants led to 7.3 times stronger inhibition of photoinduced e-/h+ recombination when compared to a benchmark P25 photocatalyst.

Near-Room-Temperature Detection of Aromatic Compounds with Inkjet-Printed Plasticized Polymer Composites.

Chemiresistive gas sensors composed of a thermoplastic polymer matrix and conductive fillers offer various advantages for detecting volatile organic compounds (VOCs), including low power consumption due to near-room-temperature operation, high sensitivity, and inherent selectivity toward VOCs. However, such sensors have a slow response time as the polymer matrix often has a glass transition temperature (Tg) higher than the sensor operating temperature slowing the analyte diffusion to/from the polymer. A plasticizer lowers polymer Tg to match the sensor operation temperature, reducing its response time. In this study, the effect of a plasticizer diethylene glycol dibenzoate (DEGDB) on the sensing properties of polystyrene (PS)-carbon black (CB) composite is investigated to obtain sensors with a fast response time and high sensitivity to VOCs. The sensors are fabricated via drop-on-demand inkjet printing, providing a high degree of control over the sensory film morphology and reproducibility. A design-of-experiment (DoE) approach is adopted to find the optimum ink and print parameters with a minimum number of experiments. As a result, sensors with 30 times faster response time and 25 times higher effective sensitivity are obtained while operating near room temperature (27 °C). Furthermore, the sensors show high sensitivity toward aromatic hydrocarbons (toluene, benzene, and ethylbenzene), with a sub-10 ppm limit of detection (LoD) and a negligible sensitivity toward humidity. Our results show the potential of PS-DEGDB-CB composite as a selective and cost-effective sensory material compatible with large-scale manufacturing techniques for selective near-room-temperature detection of toxic VOCs.

Vertical variation of source-apportioned PM2.5 and selected volatile organic compounds near an elevated expressway in an urban area.

Fine particulate matter (PM2.5) and volatile organic compounds (VOCs) are associated with adverse health effects and show spatial variation in three dimensions. The present study attempted to evaluate source contributions of PM2.5 and toxic VOCs in a metropolitan area focusing on the associated vertical variations. A special emphasis is put on the effects of the elevated expressway on the vertical variability of contribution estimates of the identified sources. Nine source factors, i.e., soil dust, sea salt/oil combustion, secondary nitrate, industrial emission, aged VOCs/secondary aerosol, traffic-related I, solvent use/industrial process, secondary sulfate, and traffic-related II, were identified using positive matrix factorization (PMF). The main contributors to PM2.5 were secondary sulfate (19.1%) and traffic-related emissions (traffic-related I and II, 16.1%), whereas the largest contributors to VOCs were traffic-related emissions (37.6%). The influence of the elevated expressway is suggested to be particularly critical on vertical variations of traffic-related emissions, including aging and secondary formation of locally accumulated air pollutants near roads. Increasing the building porosity under the viaduct could reduce the accumulation of air pollutants caused by the shelter effect. Additionally, in-street barriers would be beneficial in reducing population exposure to traffic-related emissions by altering the airflows near roads.

Interior and Exterior Surface Modification of Zr-Based Metal-Organic Frameworks for Trace Benzene Removal.

The emission of volatile organic compounds (VOCs) significantly contributes to air pollution and poses a serious threat to human health. Benzene, one of the most toxic VOCs, is difficult for the human body to metabolize and is classified as a Group 1 carcinogen. The development of efficient adsorbents for removing trace amounts of benzene from ambient air is thus of great importance. In this work, we studied the benzene adsorption properties of four Zr-based metal-organic frameworks (Zr-MOFs) through static volumetric and dynamic breakthrough experiments. Two previously reported Zr-MOFs, BUT-12 and STA-26, were prepared with a tritopic carboxylic acid ligand (H3L1) functionalized with three methyl groups, and STA-26 is a 2-fold interpenetrated network of BUT-12. Two new isoreticular Zr-MOFs, BUT-12-Et and STA-26-Et, were synthesized using a similar ligand, H3L2, where the methyl groups are replaced with ethyl groups. There are mesopores in BUT-12 and BUT-12-Et and micropores in STA-26 and STA-26-Et. The four Zr-MOFs all showed high stability in liquid water and acidic aqueous solutions. The microporous STA-26 and STA-26-Et showed much higher benzene uptakes than mesoporous BUT-12 and BUT-12-Et at room temperature under low pressures. Particularly, the benzene adsorption capacity of STA-26-Et was high up to 2.21 mmol/g at P/P0 = 0.001 (P0 = 12.78 kPa), higher than those of the other three Zr-MOFs and most reported solid adsorbents. Breakthrough experiments confirmed that STA-26-Et could effectively capture trace benzene (10 ppm) from dry air; however, its benzene capture capacity was reduced by 90% under humid conditions (RH = 50%). Coating of the crystals of STA-26-Et with polydimethylsiloxane (PDMS) increased the hydrophobicity of the exterior MOF surfaces, leading to a more than 2-fold improvement in its benzene capture capacity in the breakthrough experiment under humid condition. PDMS coating of STA-26-Et likely slowed down the water adsorption process, and thus, the adsorbent afforded more efficient capture of benzene. This work demonstrates that modifying both the interior and exterior surfaces of MOFs can effectively enhance their performance in capturing trace benzene from ambient air, even under humid conditions. This finding is meaningful for the development of new adsorbents for effective air purification applications.

Facile preparation of Au-loaded mesoporous In2O3 nanoparticles with improved ethanol sensing performance.

The in situ monitoring of toxic volatile organic compound gases using metal oxide-based gas sensors is still challenging. Herein, mesoporous In2O3 nanoparticles, assembled using smaller nanoparticles, were synthesized via a facile solvothermal method and used to load Au nanoparticles to prepare mesoporous Au/In2O3 for ethanol detection. The obtained In2O3 and Au/In2O3 were meticulously analysed by XRD, SEM, BET, TEM and XPS techniques. It was revealed that Au nanoparticles were uniformly distributed on mesoporous In2O3 nanoparticles. Notably, the obtained mesoporous 1% Au/In2O3 is highly sensitive to ethanol gas at an optimal working temperature of 180 °C, showing a response of 55 to 50 ppm of ethanol, which is considerably higher compared to that of In2O3 nanoparticles. The significantly enhanced sensitivity results from the electronic and chemical sensitization effects of Au nanoparticles. Moreover, the mesoporous Au/In2O3 nanoparticles also showed eminent selectivity, short response/recovery time, low detection limit, good linear relationship, superb repeatability, and wonderful long-term stability, suggesting that Au/In2O3 nanoparticles have great potential application for in situ monitoring of ethanol gas.

Preparation and characterization of cellulose nanofibril/chitosan aerogels with high-adsorbability and sensitive indication for indoor free formaldehyde

The toxic volatile organic compounds (VOCs), especially formaldehyde (FA), released from decoration materials pose a great threat to human health. In this study, formaldehyde adsorption performance of the specially formulated nanocellulose/chitosan aerogel (CNFCA) was investigated in simulated atmosphere. The physicochemical property of the composite aerogel was characterized, which had a large specific surface area (153.67 m2/g), a rough surface and an ultra-thin and porous structure. The composite aerogel showed excellent adsorption capacity for the formaldehyde, its theoretical maximum adsorption capacity was as high as 83.89 mg/g, and the adsorption process was more in accordance with the pseudo-second-order kinetics. The chromogenic reaction between the 4-amino-3-benzo-5-mercapto-1,2,4-triazolium (AHMT) and CNFCA was found that the color of the composite aerogel was depended on the free formaldehyde concentration. Based on this phenomenon, a colorimetric card was proposed and built to detection the formaldehyde in the atmosphere. Moreover, the adsorption mechanism research was found that the CNFCA with a multilayer structure belonged to physicochemical complex adsorption.

Cataluminescence sensor based on LaCO3OH microspheres for volatile organic compounds detection and pattern recognition

The cataluminescence (CTL) reaction detects the presence and concentration of toxic volatile organic compounds by detecting the luminescence intensity of the different components of the gas mixture. In our study, a cataluminescence online sensor system based on LaCO3OH microspheres was developed for the low concentration detection of volatile organic compounds. Multi-dimensional CTL test was carried out to analyse the correlation characteristics of heterogeneous analytes among the catalytic activity, selectivity, sensitivity, response/recover time, stability, and photoelectric signals by changing the parameters of wavelength, flow rate, temperature, and response time under the optimal conditions (280 mL/min, 180ºC, and 480 nm). Due to noise interference received by the CTL signal, the weak CTL signal was filtered based on the time-frequency characteristics of the CTL pattern signal power frequency interference and background noise. Next, this study also studied the mechanism action of the cataluminescence sensor based on LaCO3OH microspheres for gas detection, including ethyl ether, acetone, chloroform, and formaldehyde. The principal component analysis (PCA) algorithm was adopted to analyse the CTL patterns, after threshold filtering, the total variance was improved from 89.23% to 98.78% and each vapour gave its unique CTL patterns. Moreover, clustering and identification are discussed to analyse the results, including Hierarchical Cluster Analysis (HCA) and Radial Basis Function Neural Networks (RBFNN), was also discussed. The excellent cluster and recognition ability indicate the feasibility of this CTL sensor for volatile compound determination.

Oxygen vacancies rich in indium oxide hollow prism-like nanoflowers derived from NH2-MIL-68 (In) for promoted triethylamine sensing

Triethylamine (TEA) is widely viewed as the toxic volatile organic compounds and causes a severe risk to environmental protection and human health. However, the current sensors are still unable to meet the growing demand for effective and reliable detection of TEA gas. Herein, a newly designed TEA sensor based on In2O3 prism-like nanoflowers with hollow mesoporous structure is designed by directly calcining NH2-MIL-68 (In) in air atmosphere. A series of analytical techniques are performed such as BET, XPS, UV–vis, PL, EPR and Hall effect measurements. All the characterization results prove that the In2O3-400 prepared by annealing NH2-MIL-68 at 400 ℃ exhibits the maximum concentration of oxygen vacancies, the highest specific surface area, and excellent electron mobility, resulting in the best performance toward TEA. The prepared In2O3-400-based sensors possess ultrahigh response of 684.32 when exposed to 7 ppm TEA at 100 ℃ and exhibit a minimum detection limit of 0.046 ppb. The remarkable performance makes the sensors based on In2O3-400 prism-like nanoflowers become a very competitive sensing material for the detection of trace TEA vapor. The excellent selectivity, repeatability and long-term stability ensure the actual application of the prepared sensors.