Volatile Organic Compounds Emissions Research Articles

Reconfiguring closed-loop desorption for industrial solvent recycling by retaining post-condensation volatile organic compounds

Massive emissions of volatile organic compounds (VOCs) from industrial solvent evaporation have exacerbated atmospheric pollution. As high-value pollutants, VOCs can be concentrated and condensed into liquid solvents for reuse instead of destructive elimination, minimizing environmental threats and treatment costs. However, classical thermal swing adsorption (TSA) using nitrogen as the purge gas are inclined to be in closed form to economize on nitrogen, which results in desorption residues at the outlet of the adsorber and leads to environmental risks. In this study, one-step closed-loop desorption (OCD) and two-step closed-loop desorption (TCD) were proposed for industrial solvent recovery by reconfiguring TSA and condensation to improve desorption efficiency and recovery performance. A detailed mathematical model was developed and validated experimentally to describe dynamic behaviors of closed-loop desorption. The results showed that the standby adsorber connected to the thermal desorption process effectively retained the post-condensation VOCs and reduced the desorption residual for the re-absorption efficiency. By using the orthogonal experimental design, desorption temperature, condensation temperature, and feed concentration were proved to be more significant on recovery capacity than packing height and purge velocity. A broader feasible recovery domain was achieved by the TCD cycle, with an increase of 48.15 % compared to the OCD cycle at low feed concentrations. The OCD cycle was more energy-efficient, except in scenarios of low adsorption loading and low-grade energy sources. The findings provide new insights and promising approaches for achieving synergies between industrial exhaust treatment and organic solvent recovery.

Fabrication of Highly Dispersed Ru Catalysts on CeO2 for Efficient C3H6 Oxidation.

Emissions of volatile organic compounds (VOCs) threaten both the environment and human health. To realize the elimination of VOCs, Ru/CeO2 catalysts have been intensively investigated and applied. Although it has been widely acknowledged that the catalytic performance of platinum group metal catalysts was highly determined by their dispersion and coordination environment, the most reactive structures on Ru/CeO2 catalysts for VOCs oxidation are still ambiguous. In this work, starting from Ce-BTC (BTC = 1,3,5-benzenetricarboxylic acid) materials, atomically dispersed Ru catalysts and agglomerated Ru catalysts were successfully created via one-step hydrothermal method (Ru-CeO2-BTC) and conventional incipient wetness impregnation method (Ru/CeO2-BTC), respectively. In a typical model reaction of C3H6 oxidation, atomically dispersed Ruδ+ species with the formation of abundant Ru-O-Ce linkages on Ru-CeO2-BTC were found to perform much better than agglomerated RuOx species on Ru/CeO2-BTC. Further characterizations and mechanism study disclosed that Ru-CeO2-BTC catalyst with atomically dispersed Ru ions and more superior low temperature redox performance compared to Ru/CeO2-BTC could better facilitate the adsorption/activation of C3H6 and the decomposition/desorption of intermediates, thus exhibiting superior C3H6 oxidation activity. This work elucidated the reactive sites on Ru/CeO2 catalysts in the C3H6 oxidation reaction and provided insightful guidance for designing efficient Ru/CeO2 catalysts to eliminate VOCs.

Exploring exhaled breath volatile organic compounds in occupational asthma: a pilot cross-sectional study

Occupational asthma (OA) is divided into allergic asthma (AA) and irritant-induced asthma (IIA). IIA can be divided further into three different phenotypic subtypes. Volatile organic compounds (VOCs) in exhaled breath can reflect metabolic changes in the body, and a wide range of them have been associated with various diseases in the last two decades. This is the first known study to explore breath VOCs in subjects with OA, aimed to identify potential biomarkers to distinguish OA from healthy controls, as well as between different OA subgroups. In a cross-sectional investigation, exhaled breath from 40 patients with OA and 45 respiratory healthy healthcare workers were collected with ReCIVA® Breath Sampler. Samples were analyzed through an untargeted approach using thermal desorption-gas chromatography mass spectrometry (TD-GC-MS), and VOCs were identified according to tier classification. The data underwent analysis using both non-parametric and parametric statistical methods. 536 VOCs were identified. Significance (p<0.05) was observed in several emitted VOCs. Among these, compounds such as 1-hexadecanol, 2,3-butanediol, xylene, phenol, acetone, 3-methylhexane, methylcyclohexane, and isoprene have biological implications or are associated with exposures linked to OA. These VOCs may reflect metabolic changes in the body and the microbiome, as well as external exposures due to occupation.&#xD;In particular, 1-hexadecanol, 2,3-butanediol, xylene and phenol are associated with reduced nicotinamide adenine dinucleotide (NADH) and production of reactive oxygen species (ROS), mechanisms that can be linked to asthmatic diseases and therefore suggests its potential as biomarkers. This study demonstrates that VOCs detected in exhaled breath could serve as indicators of occupational exposure and enhance diagnostic accuracy for asthma.&#xD.

A comprehensive evaluation of the atmospheric impacts and health risks of cooking fumes from different cuisines

Pollutants emitted by catering enterprises pose a significant threat to the environment and public health. In this study, based on a systematic analysis of volatile organic compound (VOC) emission characteristics of different cuisines, the contribution of cooking emissions from catering enterprises to the PM2.5 and O3 concentrations in the atmosphere was evaluated using generation potential calculations and WRF-CAMx simulations. The health exposure risks of VOCs in kitchen breathing areas and those of PM2.5 and O3 contributed by the catering enterprises were evaluated. The generation potential calculation results showed that the catering enterprises exhibit 2.21–5.00 gO3/gVOCs of ozone formation potential (OFP) and 0.07–0.21 gSOA/gVOCs of secondary organic aerosol production potential (SOAP). The WRF-CAMx simulation results indicated that cooking emissions from catering enterprises contribute 0.36–1.91 μg/m3 and 0.05–0.21 μg/m3 to PM2.5 and maximum daily 8-h average (MDA8) concentrations of O3. The health exposure risks of PM2.5 and O3 were higher in catering enterprises in southern cities than in northern cities and were higher in urban areas than in suburban areas. The average hazardous VOCs (HVOCs) concentrations ranged from 53 ± 16 to 357 ± 31 μg/m3 in kitchen breathing areas. Acrolein was the primary contributor to the hazard index (HI) of all VOC species, accounting for 50.9%–99.5%. The total incremental lifetime carcinogenic risk (ILCR) of all cuisines exceeded the acceptable thresholds of 1.00 × 10−6. These findings provide insights that can aid in the formation and implementation of pollutant mitigation strategies in the catering industry.

Impact of meteorological conditions on the biogenic volatile organic compound (BVOC) emission rate from eastern Mediterranean vegetation under drought

Abstract. A comprehensive characterization of drought's impact on biogenic volatile organic compound (BVOC) emissions is essential for understanding atmospheric chemistry under global climate change, with implications for both air quality and climate model simulation. Currently, the effects of drought on BVOC emissions are not well characterized. Our study aims to test (i) whether instantaneous changes in meteorological conditions can serve as a better proxy for drought-related changes in BVOC emissions compared to the absolute values of the meteorological parameters, as indicated by previous BVOC mixing-ratio measurements and (ii) the impact of a plant under drought stress receiving a small amount of precipitation on BVOC emission rate, and on the manner in which the emission rate is influenced by meteorological parameters. To address these objectives, we conducted our study during the warm and dry summer conditions of the eastern Mediterranean region, focusing on the impact of drought on BVOC emissions from natural vegetation. Specifically, we conducted branch-enclosure sampling measurements in Ramat Hanadiv Nature Park, under natural drought and after irrigation (equivalent to 5.5–7 mm precipitation) for six selected branches of Phillyrea latifolia, the highest BVOC emitter in this park, in September–October 2020. The samplings were followed by gas chromatography–mass spectrometry analysis for BVOC identification and flux quantification. The results corroborate the finding that instantaneous changes in meteorological parameters, particularly relative humidity (RH), offer the most accurate proxy for BVOC emission rates under drought compared to the absolute values of either temperature (T) or RH. However, after irrigation, the correlation of the detected BVOC emission rate with the instantaneous changes in RH became significantly more moderate or even reversed. Our findings highlight that under drought, the instantaneous changes in RH and to a lesser extent in T are the best proxy for the emission rate of monoterpenes (MTs) and sesquiterpenes (SQTs), whereas under moderate drought conditions, T or RH serves as the best proxy for MT and SQT emission rate, respectively. In addition, the detected emission rates of MTs and SQTs increased by 150 % and 545 %, respectively, after a small amount of irrigation.

Pinewood VOC emissions protect from oxazolone-induced inflammation and dysbiosis in a mouse model of atopic dermatitis

Pinewood, increasingly used in construction and interior fittings, emits high amounts of volatile organic compounds (VOCs), which tend to accumulate in indoor air. Whether indoor VOCs affect the development of atopic dermatitis (AD) is a matter of debate. We aimed to evaluate the effects of pinewood VOCs on the development of AD-like inflammatory phenotype and linked microbiome alterations, both hallmarks of AD. An oxazolone-induced mouse model of AD was exposed to three different VOC concentrations emitted by pinewood plates throughout the experiment. The disease course and associated immunological and microbiological changes were evaluated. To validate and translate our results to humans, human keratinocytes were exposed to a synthetic pinewood VOCs mixture in an AD environment. Pinewood emitted mainly terpenes, which at a total concentration of 5 mg/m3 significantly improved oxazolone-induced key AD parameters, such as serum total IgE, transepidermal water loss, barrier gene alteration, inflammation, and dysbiosis. Notably, exposure to pinewood VOCs restored the loss of microbial richness and inhibit Staphylococci expansion characteristic of the oxazolone-induced mouse AD model. Most beneficial effects of pinewood VOCs were dose-dependent. In fact, lower (<3 mg/m3) or higher (>10 mg/m3) pinewood VOC levels maintained only limited beneficial effects, such as preserving the microbiome richness or impeding Staphylococci expansion, respectively. In the human in-vitro model, exposure of keratinocytes grown in an AD environment to a pinewood VOCs mixture reduced the release of inflammatory markers. In conclusion, our results indicate that airborne phytochemicals emitted from pinewood have beneficial effects on an AD-like phenotype and associated dysbiosis. These investigations highlight the effects of terpenes as environmental compounds in the prevention and/or control of atopic skin disease.

Identification of atmospheric emerging contaminants from industrial emissions: A case study of halogenated hydrocarbons emitted by the pharmaceutical industry

With the development of the pharmaceutical industry, halogenated hydrocarbons, which are the main raw materials and emissions of the pharmaceutical industry, may be defined as atmospheric emerging contaminants due to toxicity and low oxidation of the atmosphere. This study analyzed the volatile organic compounds (VOCs) emissions from four pharmaceutical companies located in the Yangtze River Delta. Samples were taken three times at each of the selected fixed and fugitive sampling sites in each company. Through testing, 141 VOCs were identified. The mean concentration and proportion of halogenated hydrocarbons from the four pharmaceutical companies were the highest of all the industries in the industrial park. They reached 18.9 ppm and 28.8 %, respectively. Fixed emissions of the companies exhibited the mean maximum concentration of dichloromethane and chlorobenzene, which are 11.4 ppm and 250.67 ppb. The mean concentration of fugitive emission of dichloromethane from the four companies in this study is lower than that of pharmaceutical companies in other studies. Newly detected halogenated hydrocarbons, such as 1,1-dichloropropanone and dichloronitromethane, present potential non-cancer and cancer risks to workers. Chlorobenzene was identified as a key potential cancer risk halogenated hydrocarbon the value of which reaches 0.00965. 2,6-dichloropyridine could be a potential emerging contaminant due to its lower MIR value and higher potential cancer risk. The study suggests that relevant pharmaceutical companies focus on the emissions of chlorobenzene and dichloromethane, which may be the atmospheric emerging contaminants for the pharmaceutical industry and focus on improve the treatment of waste gases in workshops and sewage stations.

Emission and odour reduction in bitumen at high temperature: A comprehensive assessment of 18 functional additives using HS-GC-MS

Bitumen additives that can reduce emissions in bitumen and asphalt are desirable for managing or mitigating harmful or odorous emissions during infrastructure projects. Assessing and comparing the relative performance of different additive classes is crucial for determining their significance in emission reduction. In this study, a range of additive classes were investigated, including commercial additives, natural products, synthetic chemicals, biomolecules, and solid adsorbents. Headspace gas chromatography-mass spectrometry (HS-GC-MS) was used to measure the release of volatile organic compounds (VOCs) from bitumen after the incorporation of these additives. Among the additives investigated, solid adsorbents such as biochar materials were the most effective in mitigating the emissions of the monitored VOCs by up to 50%. These results suggest that biochar, may be prioritized for managing VOC emissions in asphalt-related projects.

High sensitivity of nitrobenzene on the ZnO monolayer and the role of strain engineering

Volatile organic compounds (VOCs) emissions have been a recurring problem that has challenged research centers to find new ways to monitor them. From this perspective, this work investigates nitrobenzene sensing through computational simulations, a well-known toxic compound, using the strained and strain-free two-dimensional (2D) ZnO monolayer, a traditional metal oxide semiconductor (MOS). The results indicate that nitrobenzene is adsorbed via strong physisorption on the 2D ZnO and maintains interaction with the sensor under thermal stimulus (500 K), as demonstrated via ab initio molecular dynamics (AIMD) simulations. The nitrobenzene also changes the ZnO band gap energy from 4.59 to 1.85 eV and shifts 0.35 eV the work function value. Under biaxial strain, the nitrobenzene becomes chemisorbed on the ZnO monolayer. Also, remarkable conductivity changes are observed with the nitrobenzene adsorption on the strained ZnO. Excellent values of sensitivity are found, 2.29 × 1023, 8.11 × 1022 and 2.80 × 1016 for strain-free ZnO and the maximum compressed and stretched ZnO monolayer, respectively. Short recovery times of 1.16 × 10−4 s (T = 300 K) and 6.89 × 10−8 s (T = 500 K) are also found for strain-free ZnO monolayer, indicating a great reusability for nitrobenzene. Consequently, the ZnO monolayer can be used to detect nitrobenzene.

Photoinduced Evolutions of Permafrost-Derived Carbon in Subarctic Thermokarst Pond Surface Waters.

In subarctic regions, rising temperature and permafrost thaw lead to the formation of thermokarst ponds, where organics from eroding permafrost accumulate. Despite its environmental significance, limited knowledge exists regarding the photosensitivity of permafrost-derived carbon in these ponds. In this study, laboratory experiments were conducted to explore the photochemical transformations of organic matter in surface water samples from thermokarst ponds from different environments in northern Quebec, Canada. One pond near Kuujjuarapik is characterized by the presence of a collapsing palsa and is therefore organically rich, while the other pond near Umiujaq is adjacent to a collapsing lithalsa and thus contains fewer organic matters. Photobleaching occurred in the Umiujaq sample upon irradiation, whereas the Kuujjuarapik sample exhibited an increase in light absorbance at wavelength related to aromatic functionalities, indicating different photochemical aging processes. Ultrahigh-resolution mass spectrometry analysis reveals that the Kuujjuarapik sample preferentially photoproduced highly unsaturated CHO compounds with great aromaticity, while the irradiated Umiujaq sample produced a higher proportion of CHON aromatics with reduced nitrogen functionalities. Overall, this study illustrates that the photochemical reactivity of thermokarst pond water varies with the source of organic matter. The observed differences in reactivity contribute to an improved understanding of the photochemical emission of volatile organic compounds discovered earlier. Further insights into the photoinduced evolutions in thermokarst ponds may require the classification of permafrost-derived carbon therein.

Biomass-burning sources control ambient particulate matter, but traffic and industrial sources control volatile organic compound (VOC) emissions and secondary-pollutant formation during extreme pollution events in Delhi

Abstract. Volatile organic compounds (VOCs) and particulate matter (PM) are major constituents of smog. Delhi experiences severe smog during the post-monsoon season, but a quantitative understanding of VOCs and PM sources is still lacking. Here, we conduct a source apportionment study for VOCs and PM using a recent (2022), high-quality dataset of 111 VOCs, PM2.5, and PM10 in a positive matrix factorization (PMF) model. Contrasts between clean monsoon air and polluted post-monsoon air, VOC source fingerprints, and molecular tracers enabled us to differentiate paddy residue burning from other biomass-burning sources, which had previously been impossible. Burning of fresh paddy residue, as well as residential heating and waste burning, contributed the most to observed PM10 levels (25 % and 23 %, respectively) and PM2.5 levels (23 % and 24 %, respectively), followed by heavy-duty vehicles fuelled by compressed natural gas (CNG), with a PM10 contribution of 15 % and a PM2.5 contribution of 11 %. For ambient VOCs, ozone formation potential, and secondary-organic-aerosol (SOA) formation potential, the top sources were petrol four-wheelers (20 %, 25 %, and 30 %, respectively), petrol two-wheelers (14 %, 12 %, and 20 %, respectively), industrial emissions (12 %, 14 %, and 15 %, respectively), solid-fuel-based cooking (10 %, 10 %, and 8 %, respectively), and road construction (8 %, 6 %, and 9 %, respectively). Emission inventories tended to overestimate residential biofuel emissions at least by a factor of 2 relative to the PMF output. The major source of PM pollution was regional biomass burning, while traffic and industries governed VOC emissions and secondary-pollutant formation. Our novel source apportionment method even quantitatively resolved similar biomass and fossil fuel sources, offering insights into both VOC and PM sources affecting extreme pollution events. This approach represents a notable advancement compared to current source apportionment approaches, and it could be of great relevance for future studies in other polluted cities and regions of the world with complex source mixtures.

Volatile organic compound (VOC) emissions from no-added-formaldehyde lignosulphonate/pMDI particleboards and their effect on indoor air quality

ABSTRACT Wood-based panels, for example particleboards, are responsible for releasing formaldehyde and volatile organic compounds (VOCs), consequently polluting indoor air. Thus, the demand for eco-friendly wood adhesives, such as lignosulphonates (LS), has increased in detriment of the traditionally used urea-formaldehyde resins. However, combination with polymeric 4,4′-diphenylmethane diisocyanate (pMDI) is commonly proposed to minimize pressing times. In this study, particleboards were manufactured using a low lab-scale press factor of 7.5 s/mm. The adhesive contents were: 1.3% pMDI with 2.2% propylene carbonate (PC) solvent in the core layer and 15% LS in the surface layers. The VOC emissions of these boards were evaluated against those of commercial urea-formaldehyde boards. Headspace gas chromatography-mass spectrometry analysis indicated that the total VOC emissions were 66% higher for the LS/pMDI boards, comprising mainly of PC and furfural. After 14-days in a 25 L chamber, VOC emissions were examined according to ISO 16000-9:2006. LS/pMDI particleboards emitted four times more VOCs than standard boards, with 80% corresponding to PC and furfural, a suspected carcinogen. Consequently, the need for VOC quantification, even for bio-based boards is highlighted. An extension of EN 16516:2017 + A1:2020 to furniture products is also advised.

Rational design of a room‐temperature curing method, based on the epoxy–thiol click reaction, for UV‐curable hard coatings with ultrahigh strength and adhesion

AbstractIn recent years, there has been a growing demand for UV‐curable hard coatings because they offer several advantages, for example, lower energy consumption and the absence of volatile organic compound emissions. Anionic UV curing with photobase generators (PBGs), such as epoxy–thiol cross‐linking, enables curing under ambient conditions. However, designing a room‐temperature photoanionic curing system for epoxy–thiols remains challenging due to the complex effects of resin combinations on the cured products, thus making it difficult to prepare films with high hardness. Herein, we present a controlled reaction design for an anionic UV‐curing system by combining the chemical structures of epoxy resins and multifunctional thiols. The anionic UV‐curing system using PBGs that generate organic superbases demonstrated UV‐delayed curability, as evidenced by FT‐IR and photorheological analyses. To achieve high hardness, it was necessary to create the thiols with ultrarigid structures; epoxy resins with a bisphenol F structure were optimal for reacting with thiols for ultrarigid structures. This combination afforded an indentation hardness of 262 MPa with an epoxy conversion rate of 77% even at room temperature.

Biogenic Volatile Organic Compound Emission and Its Response to Land Cover Changes in China During 2001–2020 Using an Improved High‐Precision Vegetation Data Set

AbstractBiogenic volatile organic compounds (BVOCs) are regarded as important precursors for ozone and secondary organic aerosol, mainly from vegetation emissions. In the context of the expanding trend of vegetation greening, the development of high‐precision vegetation data and accurate BVOC emission estimates are essential to develop effective air pollution control measures. In this study, by integrating the multi‐source vegetation cover data, we established a high‐resolution vegetation distribution (HRVD) data set to develop a high spatio‐temporal resolution emission inventory and investigated the impact of different land cover data sets on emission simulation and impact of land cover change on BVOC emissions during 2001–2020. The annual total BVOC emissions in China for 2020 was 15.66 Tg, which were mainly from trees. The emissions simulated by CNLUCC and MODIS data sets were 1.53% and 1.72% higher than those simulated by HRVD data sets, respectively. The spatial distribution of emission differences was consistent with that of land cover differences. The simulated BVOC emissions by the HRVD data set had the best accuracy as they improved the bias between modeling and observation from 69.06% to 65.35% and decreased the underprediction of observations by a factor of 2.13 compared with simulation by MEGAN default vegetation data. The annual BVOC emissions caused by changing vegetation distribution and LAIv (LAI of vegetation covered surfaces) enhanced at a rate of 72.06 Gg yr−1 during 2001–2020. LAIv was the main driver of emission variations. The total OH reactivity of the resulted BVOC emissions increased at a rate of 1.59 s−1 yr−1, with isoprene contributed the most.

The impact of surfaces on indoor air chemistry following cooking and cleaning.

Cooking and cleaning are common sources of indoor air pollutants, including volatile organic compounds (VOCs). The chemical fate of VOCs indoors is determined by both gas-phase and multi-phase chemistry, and can result in the formation of potentially hazardous secondary pollutants. Chemical interactions at the gas-surface boundary play an important role in indoor environments due to the characteristically high surface area to volume ratios (SAVs). This study first characterises the VOC emissions from a typical cooking and cleaning activity in a semi-realistic domestic kitchen, using real-time measurements. While cooking emitted a larger amount of VOCs overall, both cooking and cleaning were sources of chemically reactive monoterpenes (peak mixing ratios 7 ppb and 2 ppb, respectively). Chemical processing of the VOC emissions from sequential cooking and cleaning activities was then simulated in a kitchen using a detailed chemical model. Results showed that ozone (O3) deposition was most effective onto plastic and soft furnishings, while wooden surfaces were the most effective at producing formaldehyde following multi-phase chemistry. Subsequent modelling of cooking and cleaning emissions using a range of measured kitchen SAVs revealed that indoor oxidant levels and the subsequent chemistry, are strongly influenced by the total and material-specific SAV of the room. O3 mixing ratios ranged from 1.3-7.8 ppb across 9 simulated kitchens, with higher concentrations of secondary pollutants observed at higher O3 concentration. Increased room volume, decreased total SAV, decreased SAVs of plastic and soft furnishings, and increased wood SAV contributed to elevated formaldehyde and total peroxyacetyl nitrates (PANs) mixing ratios, of up to 1548 ppt and 643 ppt, respectively, following cooking and cleaning. Therefore, the size and material composition of indoor environments has the potential to impact the chemical processing of VOC emissions from common occupant activities.

Greenhouse gas and volatile organic compound emissions of additive-treated whole-plant maize silage: part A—anaerobic fermentation period

BackgroundSilage emits climate- and environment-relevant gases during fermentation and feed-out periods. This trial aimed to determine the unknown carbon dioxide (CO2), methane, nitrous oxide, ethanol, and ethyl acetate emissions of constant maize silage material over both periods. The results will be published in two consecutive articles (Part A: anaerobic fermentation period, Part B: aerobic storage period).MethodsThe untreated control (CON) was compared with the chemical additive treatment (CHE; 0.5 g sodium benzoate and 0.3 g potassium sorbate per kg fresh matter) and the biological additive treatment (BIO; 108 colony-forming units (CFU) Lentilactobacillus buchneri and 107 CFU Lactiplantibacillus plantarum per kg fresh matter). Barrel silos (n = 4) were connected to gas bags to quantify gas formation during anaerobic fermentation (30 or 135 ensiling days). Glass jar silos (n = 12) were used for laboratory silage analysis.ResultsCHE produced significantly (p < 0.05) less gas (6.7 ± 0.3 L per kg dry matter ensiled material (kgDM) until ensiling day 14.0 ± 0.0) and ethanol (8.6 ± 1.5 mg kgDM–1) than CON did (8.5 ± 0.2 L kgDM–1 until ensiling day 19.5 ± 6.4; 12.2 ± 1.5 (mg ethanol) kgDM–1). BIO indicates prolonged gas formation (9.1 ± 0.9 L kgDM–1 until ensiling day 61.3 ± 51.9; 12.0 ± 2.1 mg kgDM–1). CO2 is the main component of the gas formed. All treatments formed methane and nitrous oxide in small quantities. CON emitted significantly more CO2eq emissions than BIO and less than CHE (p < 0.05). Additives had no effect on ethyl acetate gas emissions. For BIO, ethanol concentrations in the material (rS = 0.609, p < 0.05) and gas quantities (rS = 0.691, p < 0.05) correlate with ethyl acetate gas quantities. All the treatments exhibited decreasing gas and CO2 quantities, and the dry matter mass increased between ensiling days 14 and 30 (− 0.810 ≤ rS ≤ 0.442; p < 0.05 to p = 0.20).ConclusionSilage generates climate- and environmental-relevant gases during fermentation and silage additives affect this pattern. Gas formation exceeds the fixation potential, and the carbon footprint of silage fermentation is negative.Graphical

VOC emission rates from an indoor surface using a flux chamber and PTR-MS

Arising from the Chemical Assessment of Surfaces and Air (CASA) 2022 study at the National Institute of Standards and Technology (NIST) Net-Zero Energy Residential Test Facility (NZERTF), this paper presents the first evaluation of indoor surface emissions to a house measured with a surface flux chamber coupled to an online, non-targeted volatile organic compound (VOC) mass spectrometric detection. These surface emissions are compared to those assessed using ambient, whole house indoor VOC measurements and the outdoor air change rate. Chamber emission rates varied by almost four orders of magnitude across 35 quantified VOCs. The whole house emissions measured by campaign-long ambient measurements and the flux chamber emissions (when scaled to the painted surface area of the house) are similar, with an average ratio between the two of 1.3 ± 1.0. The general agreement between these two approaches indicates that the flux chamber was not solely measuring primary emissions from building materials located below the chamber. Rather, the results suggest that over the 12-year house lifetime, VOCs have been widely distributed around the house, migrating from their primary sources to secondary surface reservoirs. With the house in a quasi-steady state, the thermodynamic activities (i.e., the vapor pressures) of the VOCs within the different reservoirs become similar. Emissions of aromatics and monoterpenes have declined since the house was built, whereas aldehyde emissions have remained relatively constant.

Dynamics of indoor volatile organic compounds and seasonal ventilation strategies for residential buildings in Northeast China

This study utilized a questionnaire survey to collect data from 265 residents in Changchun, encompassing building characteristics, ventilation frequency and overall satisfaction with the indoor environment. Statistical analysis revealed significant disparities in ventilation frequency and satisfaction with indoor temperature. The survey results indicate that the primary mode of indoor air exchange amongst Changchun residents is window ventilation, accounting for 93%. Field tracking was conducted to measure indoor air concentrations of volatile organic compounds (VOCs) in residential buildings during winter and summer seasons. The study revealed a significant increase in the average indoor/outdoor (I/O) ratio of the targeted 25 VOC concentrations in winter, rising from 10.8 to 17.7. The findings underscore indoor sources as predominant contributors to the measured VOCs. Temperature, humidity and room functions are the main factors affecting VOC concentration. Higher temperatures and increased relative humidity both contributed to elevated indoor VOC levels. This study recommended the opening of more windows during high temperature and high humidity in summer, to maintain good indoor air quality and effectively age the emission of VOCs from furniture. This study contributes to the enhancement of the database on indoor air quality and effective ventilation strategies in cold regions for safeguarding public health.

Suprathreshold Water Spray Stimulus Enhances Plant Defenses against Biotic Stresses in Tomato.

Mechanical stimuli can affect plant growth, development, and defenses. The role of water spray stimulation, as a prevalent mechanical stimulus in the environment, in crop growth and defense cannot be overlooked. In this study, the effects of water spray on tomato plant growth and defense against the chewing herbivore Helicoverpa armigera and necrotrophic fungus Botrytis cinerea were investigated. Suprathreshold water spray stimulus (LS) was found to enhance tomato plant defenses against pests and pathogens while concurrently modifying plant architecture. The results of the phytohormone and chemical metabolite analysis revealed that LS improved the plant defense response via jasmonic acid (JA) signaling. LS significantly elevated the level of a pivotal defensive metabolite, chlorogenic acid, and reduced the emissions of volatile organic compounds (VOCs) from tomato plants, thereby defending against pest and pathogen attacks. The most obvious finding to emerge from this study is that LS enhances tomato plant defenses against biotic stresses, which will pave the way for further work on the application of mechanical stimuli for pest management.

Intercropping Alters Phytochemical Defenses Against Insect Herbivory.

Given the multiple possible mechanisms for interspecific chemical interaction between adjacent heterospecific plants, phytochemical defenses of pest-susceptible crop species could potentially be enhanced or altered by intercropping with phytochemically diverse neighbors. We assessed the influence of intercropping between phytochemically diverse plants on aerial volatile organic compound (VOC) emission profiles by intercropping Melilotus alba and Triticum aestivum with Silphium integrifolium in AMF-inoculated soil. We also assessed the impact of intercropping on induced plant defenses by conducting an in-situ, no-choice bioassay with Spodoptera frugiperda. Of eight compound classes we identified across the three plant species, prenol lipids (terpenoids) were upregulated in silflower plants when monocropped with wheat and when herbivory was induced. Carboxylic acids and organooxygen compounds were reduced in sweetclover when intercropped with silflower, but increased under herbivory. Uninfested wheat plants emitted more organooxygen compounds and fatty acyls than infested plants when intercropped with silflower, but not when monocropped. This study showed that VOC emissions of plants from three diverse taxa are altered by both intercropping and herbivory in ways that may impact their resistance to insect herbivory. Further research into the role of intercropping on pest resistance in agroecological systems could help farmers to design intercropping systems that optimize natural plant herbivory defenses, thus improving agricultural sustainability.