Loss Of Volatile Organic Compounds Research Articles

Short-term storability of volatile organic compounds in bag sampling systems under ambient conditions

Although bag sampling is a common quantification tool for volatile organic compounds (VOCs), it can serve as a major source of experimental bias, when storing even over a short duration (< 24 hours). To learn more about the reliability of the bag sampling method, the temporal stability of 27 VOCs (classified into five groups (i.e., aldehydes, nonpolar aromatic hydrocarbons, aliphatic carboxylic acids, phenol and methylphenols, and miscellaneous odorants) is assessed using poly-ester aluminum (PEA) bags at five intervals over a day (0.17, 1, 2, 6, and 24 hours). In terms of reproducibility (e.g., relative standard error [RSEt, %]), nonpolar aromatic hydrocarbons (BTXS) exhibit the highest consistency (e.g., average RSE < 1.55%). Considerable loss of VOCs is observed in the preparation of gaseous standards from a liquid phase standard when assessed by gas/liquid (G/L) ratio. Further, VOCs with lower molecular weights (e.g., propionaldehyde: 77% - 94.4%) and branched molecular structures (e.g., isovaleraldehyde: 67.2% - 78.9%) tend to have high G/L ratio (e.g., relative to valeraldehyde with 55.1% - 66%). The overall relative recovery (RR; %) values of VOCs indicatean exponential decrease over 24 hours. BTXS maintain fairly good RR values (above 94.3% at all intervals), possibly due to the nonpolar structure with uniform distribution of π electrons. In contrast, indole and skatole show the least preservation after 24 hr (e.g., RR4 values of 10.9% and 24.6%, respectively) due to their highly reactive characteristics. The storability of VOCs appears to be affected by a number of variables (e.g., molecular weight, presence of ethyl branch, and time: e.g., R2 > 0.9). The results of this study offer valuable guidelines for the accurate quantification of VOC levels in air.

Changes in factor profiles deriving from photochemical losses of volatile organic compounds: Insight from daytime and nighttime positive matrix factorization analyses

Substantial effects of photochemical reaction losses of volatile organic compounds (VOCs) on factor profiles can be investigated by comparing the differences between daytime and nighttime dispersion-normalized VOC data resolved profiles. Hourly speciated VOC data measured in Shijiazhuang, China from May to September 2021 were used to conduct study. The mean VOC concentration in the daytime and at nighttime were 32.8 and 36.0 ppbv, respectively. Alkanes and aromatics concentrations in the daytime (12.9 and 3.08 ppbv) were lower than nighttime (15.5 and 3.63 ppbv), whereas that of alkenes showed the opposite tendency. The concentration differences between daytime and nighttime for alkynes and halogenated hydrocarbons were uniformly small. The reactivities of the dominant species in factor profiles for gasoline emissions, natural gas and diesel vehicles, and liquefied petroleum gas were relatively low and their profiles were less affected by photochemical losses. Photochemical losses produced a substantial impact on the profiles of solvent use, petrochemical industry emissions, combustion sources, and biogenic emissions where the dominant species in these factor profiles had high reactivities. Although the profile of biogenic emissions was substantially affected by photochemical loss of isoprene, the low emissions at nighttime also had an important impact on its profile. Chemical losses of highly active VOC species substantially reduced their concentrations in apportioned factor profiles. This study results were consistent with the analytical results obtained through initial concentration estimation, suggesting that the initial concentration estimation could be the most effective currently available method for the source analyses of active VOCs although with uncertainty.

Characteristic, source apportionment and effect of photochemical loss of ambient VOCs in an emerging megacity of Central China

During the transportation from emission sources to sampling site, volatile organic compounds (VOCs) undergo photochemical losses which have significant effects for tropospheric ozone (O3) formation and VOCs source apportionment. In this study, based on hourly speciated VOC data from May 23, to July 8, 2019 with high O3 concentrations, the concentration level, chemical composition, and diurnal variation of observed VOCs were studied, and the initial concentration of VOCs was obtained by combining the local emission inventory in Zhengzhou, Central China. The impact of photochemical loss on source apportionment was evaluated using the Positive Matrix Factorization/Multilinear Engine 2-Species Ratio (PMF/ME2-SR) model based on observed and initial VOCs concentration (OC-PMF and IC-PMF). Results suggest that during the observed period, the average concentration of total VOCs (TVOCs) was 23.74 ± 9.20 ppbv, and alkanes (3.92 ± 2.40 ppbv) were the predominant component. The photochemical losses of TVOCs were approximately 10.15 ± 7.13 ppbv, with an average loss rate of 29.9%. The ozone formation potential (OFP) based on the initial VOCs concentration was 2.2 times higher than that observed VOCs concentration. Alkenes contributed the most to OFP and were also the largest contributors to photochemical losses. TVOC concentrations increased by 5.0% during O3 pollution compared to non-O3 pollution. Seven sources of VOCs were determined, including biomass burning, liquefied petroleum gas (LPG), vehicle emission, industrial emission, solvent usage, gasoline evaporation, and biogenic emission. Compared to the results of IC-PMF, the contributions of these sources in OC-PMF were underestimated by 15.4%, 14.4%, 13.0%, 11.7%, 31.5%, 7.6%, and 4.7%, respectively. This study still exhibits certain limitations in calculation method, and further exploration can be conducted in the future.

Roles of photochemical consumption of VOCs on regional background O3 concentration and atmospheric reactivity over the pearl river estuary, Southern China

Understanding of the photochemical ozone (O3) pollution over the Pearl River Estuary (PRE) of southern China remains limited. We performed an in-depth analysis of volatile organic compounds (VOCs) data collected on an island (i.e., the Da Wan Shan Island, DWS) located at the downwind of Pearl River Delta (PRD) from 26 November to 15 December 2021. Abundances of O3 and its precursors were measured when the air masses originated from the inland PRD. We observed that the VOCs levels at the DWS site were lower, while the mixing ratio of O3 was higher, compared to those reported at inland PRD, indicating the occurrence of photochemical consumption of VOCs during the air masses transport, which was further confirmed by the composition and diurnal variations of VOCs, as well as ratios of specific VOCs. The simulation results from a photochemical box model showed that the O3 level in the outflow air masses of inland PRD (O3(out-flow)) was the dominant factor leading to the intensification of O3 pollution and the enhancement of atmospheric radical concentrations (ARC) over PRE, which was mainly contributed by the O3 production via photochemical consumption of VOCs during air masses transport. Overall, our findings provided direct quantitative evidence for the roles of outflow O3 and its precursors from inland PRD on O3 abundance and ARC over the PRE area, highlighting that alleviation of O3 pollution over PRE should focus on the impact of photochemical loss of VOCs in the outflow air masses from inland PRD.

Highly efficient diluent-free solvent extraction of uranium using mixtures of protonated trioctylamine and quaternary ammonium salts. Comparative Life Cycle Assessment with the conventional extractant

A more environmentally friendly solvent extraction process was formulated for uranium extraction using diluent-free extractants based on trialkylammonium compounds. The effect of ammonium cations and anions toward extraction efficiency, viscosity and phase separation was also evaluated. These systems were shown to be highly efficient and simple to implement as they rely on the same chemical components as those applied in the actual industrial process. It has also been demonstrated that using such alternatives allows not only to prevent third phase formation and subsequent extractant degradation, but also reduces the evaporation loss of solvent by a factor of 20. Among the systems investigated, the pure [TOAH]2[SO4] was selected as the simplest and most efficient. A comparative Life Cycle Assessment (LCA) was also conducted between this system and the conventional solvent to compare more objectively their sustainability. Results based on four environmental indicators show that the new system is 18 times less impactful. Contrary to expectations, this study also showed that the pure (diluent-free) extractant system needs to be at least 2 times more efficient in terms of metal extraction to become significantly more sustainable. Other main effects contributing to the LCA are derived from: (i) the production of chemicals, which is much more harmful for extractants than for aliphatic diluents, (ii) the loss of Volatile Organic Compounds (VOC) to the environment, and (iii) to a lesser extent, the additional centrifugation step that may be required to separate more viscous systems.

The importance of photochemical loss to source analysis and ozone formation potential: Implications from in-situ observations of volatile organic compounds (VOCs) in Guangzhou, China

The chemical loss of volatile organic compounds (VOCs) is influenced by atmospheric and is closely related to the photochemical formation of ozone (O3). Therefore, research on the atmospheric chemical transformation of VOCs is essential to understand their contribution to O3 formation. This study collected data on photochemical-related atmospheric components and meteorological factors in spring at a typical comprehensive observation platform in Guangzhou, China. The photochemical age method was used to evaluate the loss of VOCs due to atmospheric photochemical transformation and to analyze the contribution of such transformation to the source apportionment of VOCs and to the ozone formation potential (OFP). The results show that the mean photochemical loss of total volatile organic compounds (TVOCs) during the observation period was 4.1 ppbv, accounting for approximately 15% of the initial TVOC content. Alkenes had the highest consumed concentration/initial concentration (C/I ratio) of 37.3%. A comparison of the source apportionment results obtained using observational positive matrix factorization (Ob-PMF) and in situ positive matrix factorization (In-PMF) revealed that photochemical losses significantly affected VOCs emitted from industrial and biological sources. Furthermore, neglecting the photochemical loss of VOCs in PMF source apportionment could lead to an underestimation of the contribution of VOCs from industrial and biological sources. The calculated values of OFP under VOC loss (OFPC–VOCs) showed that OFPC-VOCs constituted approximately 30% of the OFP of the initial VOCs. 93.2% of the OFP was attributed to the photochemical loss of alkenes and aromatic hydrocarbons, indicating their significant influence on O3 formation. This study emphasizes the importance of fully considering the photochemical loss of VOCs for accurately assessing their sources and contributions to ozone pollution. It also provides theoretical support for formulating VOC emission reduction strategies in the Pearl River Delta region.

Characterization of photochemical losses of volatile organic compounds and their implications for ozone formation potential and source apportionment during summer in suburban Jinan, China

Volatile organic compounds (VOCs) undergo substantial photochemical losses during their transport from emission sources to receptor sites, resulting in serious implications for their source apportionment and ozone (O3) formation. Based on the continuous measurements of VOCs in suburban Jinan in August 2022, the effects of photochemical losses on VOC source contributions and O3 formation were evaluated in this study. The observed and initial concentrations of total VOCs (TVOC) were 12.0 ± 5.1 and 16.0 ± 7.4 ppbv, respectively. Throughout the observation period, alkenes had the most prominent photochemical losses (58.2%), followed by aromatic hydrocarbons (23.1%), accounting for 80.6% and 6.9% of the total losses, respectively. During high O3 episodes, the photochemical loss of VOCs was 6.9 times higher than that during the cleaning period. Alkene losses (exceeding 67.3%), specifically losses of isoprene, propylene, ethylene, and n-butene, dominated the total losses of VOCs during the O3 increase period. Eight sources of VOCs were identified by positive matrix factorization (PMF) based on the observed and initial concentration data (OC-PMF and IC-PMF, respectively). Concentrations of all emission sources in the OC-PMF were underestimated by 2.4%–57.1%. Moreover, the contribution of each emission source was over- or underestimated compared with that in case of the IC-PMF. The contributions of biogenic and motor vehicle exhaust emissions were underestimated by 5.3 and 2.8 percentage points, respectively, which was associated with substantial oxidation of the emitted high-reactive species. The contributions of coal/biomass burning and natural gas were overestimated by 2.4 and 3.9 percentage points, respectively, which were related to the emission of low-reactive species (acetylene, ethane, and propane). Based on our results, the photochemical losses of VOCs grossly affect their source apportionment and O3 formation. Thus, photochemical losses of VOCs must be thoroughly accounted to establish a precise scientific foundation for air-pollution control strategies.

Atmospheric oxidation capacity and secondary pollutant formation potentials based on photochemical loss of VOCs in a megacity of the Sichuan Basin, China

Volatile organic compounds (VOCs) are significant precursors to photochemical pollution. However, reactive VOC species are easily oxidized during transportation, resulting in a systematic underestimate of the measured concentrations. To address this, we applied an improved calculation method to correct the measured VOC concentrations into photochemical initial concentrations (PICs) in Chengdu, a megacity in the Sichuan Basin, China, which is highly vulnerable to complex pollution. In this study, 56 VOC species on the Photochemical Assessment Monitor Station (PAMS) target list were quantitatively monitored throughout all four seasons. Comparing to directly measured values, photochemically initialized total mixing ratios of VOCs increased by 18.6 % in general. The photochemical loss percentages of alkenes and aromatics were prominent in summer (68.6 %, 28.7 %) and spring (65.9 %, 24.7 %), respectively. Furthermore, we examined contributions of VOCs to atmospheric oxidation capacity (AOC) depending on PICs and found that maximum daily total AOC showed a surge in spring and summer. Besides hydroxyl radicals, daytime O3 in spring and late-afternoon nitrate radicals in summer were essential for AOC with PICs. As expected, alkenes and aromatics dominated PIC-based ozone formation potentials (OFPs). Furthermore, contribution of alkenes to secondary organic aerosol formation potentials reached 15.5 % and 7.6 % in spring and summer, respectively. Using positive matrix factorization model, we identified five VOC sources including vehicular exhaust, industrial emissions, solvent usage, biogenic sources, and liquefied petroleum gas/natural gas use. Based on PICs, biogenic sources were significantly underestimated in spring and summer. Meanwhile, m,p-xylene from solvent usage and isoprene from biogenic sources were the primary contributors to OFPs. Consequently, these results emphasize the significance of photochemically oxidized VOC concentrations, especially for reactive species in typical seasons.

Source apportionment and ozone formation mechanism of VOCs considering photochemical loss in Guangzhou, China

Understanding the sources and impact of volatile organic compounds (VOCs) on ozone formation is challenging when the traditional method does not account for their photochemical loss. In this study, online monitoring of 56 VOCs was carried out in summer and autumn during high ozone pollution episodes. The photochemical age method was used to evaluate the atmospheric chemical loss of VOCs and to analyze the effects on characteristics, sources, and ozone formation of VOC components. The initial concentrations during daytime were 5.12 ppbv and 4.49 ppbv higher than the observed concentrations in the summer and autumn, respectively. The positive matrix factorization (PMF) model identified 5 major emission sources. However, the omission of the chemical loss of VOCs led to underestimating the contributions of sources associated with highly reactive VOC components, such as those produced by biogenic emissions and solvent usage. Conversely it resulted in overestimating the contributions from VOC components with lower chemical activity such as liquefied petroleum gas (LPG) usage, vehicle emissions, and gasoline evaporation. Furthermore, the estimation of ozone formation may be underestimated when the atmospheric photochemical loss is not taken into account. The ozone formation potential (OFP) method and propylene-equivalent concentration method both underestimated ozone formation by 53.24 ppbv and 47.25 ppbc, respectively, in the summer, and by 40.34 ppbv and 26.37 ppbc, respectively, in the autumn. The determination of the ozone formation regime based on VOC chemical loss was more acceptable. In the summer, the ozone formation regime changed from the VOC-limited regime to the VOC-NOx transition regime, while in the autumn, the ozone formation regime changed from the strong VOC-limited regime to the weak VOC-limited regime. To obtain more thorough and precise conclusions, further monitoring and analysis studies will be conducted in the near future on a wider variety of VOC species such as oxygenated VOCs (OVOCs).

The effect of drying, cell disruption and storage on the sensory properties of Nannochloropsis sp.

Adding microalgae into food could strongly influence the flavor of the final product which is the key factor for consumer acceptation. To assist food processors in the development of tasteful food products containing microalgae, it is necessary to understand the impact of processing and storage on the flavor of freshly harvested microalgae biomass. In this study, the effect of commonly used drying techniques (freeze-drying, spray drying and thin-layer oven drying) and cell disruption (high pressure homogenization) on the sensory quality of fresh Nannochloropsis sp. biomass was investigated. Furthermore, the impact of storage on the flavor properties of intact (non-disrupted) and disrupted Nannochloropsis paste was examined. Sensory evaluation by a trained panel indicated that the flavor of Nannochloropsis was not affected by freeze-drying. Whereas thin-layer oven drying at 60 °C resulted in a strong bitter taste and a musty odor. This odor is positively correlated with volatile organic compounds (VOCs) including Strecker aldehydes that arise from the Strecker degradation in the course of the Maillard reaction. Spray drying reduced the odor intensity and grassy odor of Nannochloropsis which could be attributed to the loss of several VOCs including esters, saturated alcohols and dimethyl sulfide. Furthermore, cell disruption of Nannochloropsis using high pressure homogenization resulted in intense grassy and fish oil odors features due to high amounts of fatty acid-derived unsaturated aldehydes, ketones and alcohols. Finally, dark storage of fresh intact and disrupted Nannochloropsis paste at ambient temperature strongly impacts the volatile profile due to the rapid formation of several VOCs, which negatively impact the palatability of the Nannochloropsis biomass. Our results provide the basis to be applied in downstream food processing of harvested Nannochloropsis biomass in order to maintain or optimize the flavor properties for specific food products.

Quantitative evidence from VOCs source apportionment reveals O3 control strategies in northern and southern China

Ground-level ozone (O3) pollution has received widespread attention because its rising trend and adverse ecological impacts. However, the extremely strong photochemical reactions of its precursor volatile organic compounds (VOCs) increase the difficulty of reducing VOCs emissions to alleviate O3. Here, we carried out a one-year comprehensive observation in two representative cities, Tianjin (TJ, Northern China) and Guangzhou (GZ, Southern China). By revealing the concentration characteristics of three different types of VOCs, i.e., initial VOCs without photochemical reaction (In-VOCs), consumed VOCs (C-VOCs), and measured VOCs after the reaction (M-VOCs), we elucidated the important role of C-VOCs in the formation of O3. Although the overall trends were similar in both cities, the average concentration level of VOCs in GZ was 8.2 ppbv higher than that in TJ, and the photochemical loss of VOCs was greater by 2.2 ppbv. In addition, various drivers affecting O3 generation from C-VOCs were specifically explored, and it was found that most alkenes of TJ were key substances for rapid O3 formation compared to aromatics of GZ. Meanwhile, favorable meteorological conditions such as high temperature (T > 31 °C in TJ, and T > 33 °C in GZ), low relative humidity (56% in TJ and 45% in GZ), and stable atmospheric environment (proper pressure and gentle wind speed) also contribute to the generation of O3. More importantly, we combined chemical kinetics and receptor model to quantify the three-type VOCs source contributions and assess the potential impact of C-VOCs sources on O3 production, thus proposing environmental abatement technologies corresponding to the three types of VOCs. The differences in the comparison results of the three-type VOCs highlight the need to reduce O3 pollution from C-VOCs sources, which provides insights for future clean air policies development.

Effect of photochemical losses of ambient volatile organic compounds on their source apportionment

Photochemical losses of ambient volatile organic compounds (VOCs) substantially affect source apportionment analysis. Hourly speciated VOC data measured from April to August 2020 in Tianjin, China were used to analyze the photochemical losses of VOC species and assess the impacts of photochemical losses on source apportionment by comparing the positive matrix factorization (PMF) results based on observed and initial concentration data (OC-PMF and IC-PMF). The initial concentrations of the VOC species were estimated using a photochemical age-based parameterization method. The results suggest that the average photochemical loss of total VOCs (TVOCs) during the ozone pollution period was 2.4 times higher than that during the non-ozone pollution period. The photochemical loss of alkenes was more significant than that of the other VOC species. Temperature has an important effect on photochemical losses, and different VOC species have different sensitivities to temperature; high photochemical losses mainly occurred at temperatures between 25 °C and 35 °C. Photochemical losses reduced the concentrations of highly reactive species in the OC-PMF factor profile. Compared with the IC-PMF results, the OC-PMF contributions of biogenic emissions and polymer production-related industrial sources were underestimated by 73 % and 50 %, respectively, likely due to the oxidation of isoprene and propene, respectively. The contribution of diesel and gasoline evaporation was underestimated by 39 %, which was likely due to the loss of m,p-xylene. Additionally, the contributions of liquefied petroleum gas, vehicle emissions, natural gas, and oil refinery were underestimated by 31 %, 29 %, 23 %, and 13 %, respectively. When the O3 concentrations were higher than 140 μg m−3 or the temperatures were higher than 30 °C, the photochemical losses from most sources increased substantially. Additionally, solar radiation produced different photochemical losses for different source types.

Source apportionment of VOCs based on photochemical loss in summer at a suburban site in Beijing

Volatile organic compounds (VOCs) are critical precursors of photochemical smog. Quantitatively evaluating the VOC sources and their contributions to ozone formation provides valuable information for photochemical pollution abatement. However, due to the fast oxidization of VOCs during transport in the atmosphere, source apportionment via receptor models using measured VOC data inevitably has a systematic deviation. In this study, we conducted a field measurement of VOCs at a suburban site in Beijing and evaluated the influences of photochemical oxidization on VOC source contributions. The initial VOC concentration, defined as the sum of measured VOC concentration and their photochemical losses. The real-time photochemical age-based parameterization method and a sequential reaction model were applied to characterize the photochemical loss of VOCs. Also, the photochemical loss of VOCs was considered in the he positive matrix factorization (PMF) model. Photochemical losses, on average, accounted for 5.6% of total VOCs (TVOCs) and 59.2% of alkenes, indicating that the impact of photochemical reaction cannot be ignored. Alkanes were the most significant contributors to both measured and initial TVOCs, while the alkenes and oxygenated volatile organic compounds (OVOCs), especially ethylene and isoprene, contributed the most to ozone formation potential. By adopting the positive matrix factorization model, seven VOC sources were identified for both measured and initial TVOCs. Vehicular emissions, industrial sources, and biomass burning were the top three contributors to ambient TVOC. Photochemistry significantly influenced the results of source apportionment, e.g., the contribution of biogenic sources (+4.4%), industrial emissions (+2.5%) and solvent usage (+2.5%) based on initial VOCs were larger than that of measured VOCs, while the contribution of gasoline vehicular emissions (−9.9%) was lower than that of measured VOCs. Our results highlight the necessity of adequately considering the photochemical loss of VOCs for accurately apportioning the emission sources.

Analysis of potential migration compounds from silicone molds for food contact by SPME-GC-MS

Four commercially available silicone cupcake molds have been studied. An evaluation of the post-cure treatment applied to the silicone molds was carried out and the loss of volatile organic compounds after cure treatment was quantified. The two higher quality molds showed losses at the 0.5% (w/w) (recommended by BfR standard), while the two lower quality molds exceeded this limit.The migration studies were carried out using Tenax® as a solid food simulant. The volatile compounds that migrate were identified and quantified using SPME-GC-MS. Up to fourteen silicone oligomers were quantified. When the molds were subjected to post-cure treatment, none of them exceeded the global migration of 10 mg/dm2; while those lower quality molds showed migrations higher than 10 mg/dm2, so their use in contact with food is not recommended.

Environmental and human health risks of plastic composites can be reduced by optimizing manufacturing conditions

New plastic composites are being manufactured outdoors, inside buried water and sewer pipes. This cured-in-place-pipe (CIPP) practice has been less expensive than other infrastructure repair options, but pollutants discharged during and after plastic manufacture pose environmental and human health problems. The study goal was to better understand how composite manufacturing conditions could be altered to reduce the amount of pollution released. Initiator loading, curing time, and curing pressure were modified for CIPP styrene and non-styrene ("HAP and VOC free") resin based composites. The styrene resin contained 39 wt% volatile organic compounds (VOC) whereas the non-styrene resin contained 4 wt% VOCs. Both resins contained hazardous air pollutants (HAP), endocrine disruptor, and carcinogenic compounds not listed on their safety data sheets. Vacuum pressure prompted greater VOC loss from the resins compared to ambient pressure manufacture. During both pressure manufacturing conditions, less than 1 wt% VOC was released from non-styrene composites into air compared to 8.8 to 26.4 wt% VOC released from styrene composites. VOCs including acetophenone, dibutyl maleate, p,α-dimethylstyrene, ethylbenzene, isopropylbenzene, methacrylic acid, 2-phenyl-2-propanol, styrene, toluene, and m-xylene were present in the non-styrene composite after manufacture. By doubling the styrene composite's initiator loading, styrene and styrene oxide residuals were reduced by 42 and 33 wt%, respectively. Manufacturer recommended conditions for the non-styrene composite resulted in <1 wt% initiator usage. The life cycle environmental impact assessment, which considered only composite VOC residual, predicted that styrene dominantly influenced ecotoxicity and human carcinogenic levels. Modifications to CIPP resin composition and the curing process can reduce environmental and human health impacts.

Influence of photochemical loss of volatile organic compounds on understanding ozone formation mechanism

Abstract. Volatile organic compounds (VOCs) tend to be consumed by atmospheric oxidants, resulting in substantial photochemical loss during transport. An observation-based model was used to evaluate the influence of photochemical loss of VOCs on the sensitivity regime and mechanisms of ozone formation. Our results showed that a VOC-limited regime based on observed VOC concentrations shifted to a transition regime with a photochemical initial concentration of VOCs (PIC-VOCs) in the morning. The net ozone formation rate was underestimated by 3 ppb h−1 (∼36 ppb d−1) based on the measured VOCs when compared with the PIC-VOCs. The relative contribution of the RO2 path to ozone production based on the PIC-VOCs accordingly increased by 13.4 %; in particular, the contribution of alkene-derived RO2 increased by approximately 10.2 %. In addition, the OH–HO2 radical cycle was obviously accelerated by highly reactive alkenes after accounting for photochemical loss of VOCs. The contribution of local photochemistry might be underestimated for both local and regional ozone pollution if consumed VOCs are not accounted for, and policymaking on ozone pollution prevention should focus on VOCs with a high reactivity.

Improved positive matrix factorization for source apportionment of volatile organic compounds in vehicular emissions during the Spring Festival in Tianjin, China

Photochemical losses of volatile organic compounds (VOCs) and uncertainties in calculated factor profiles can reduce the accuracy of source apportionment by positive matrix factorization (PMF). We developed an improved PMF method (termed ICLP-PMF) that estimated the reaction-corrected (“initial”) concentrations of VOCs. Source profiles from literature provided constraints. ICLP-PMF evaluated the vehicular emission contributions to hourly speciated VOC data from December 2020 to March 2021 and estimated gasoline and diesel vehicles contributions to Tianjin's VOC concentrations around the Chinese Spring Festival (SF). The average observed and initial total VOCs (TVOCs) concentrations were 24.2 and 42.9 ppbv, respectively. Alkanes were the highest concentration VOCs while aromatics showed the largest photochemical losses during the study period. Literature gasoline and diesel profiles from representative Chinese cities were constructed and provided constraints. Source apportionment was performed using ICLP-PMF method and three other PMF approaches. Photochemical losses of alkenes and aromatic hydrocarbons induced differences between calculated factor profiles and literature profiles. Using observed concentrations and unconstrained profiles produced underestimated SF contributions (∼121% and 72% for gasoline and diesel vehicles, respectively). According to the ICLP-PMF results, the contributions of gasoline and diesel vehicles during the SF were 25.6% and 23.2%, respectively, lower than those before and after the SF. No diel diesel vehicle contribution variations were found during the SF likely due to the decline in truck activity north of the study site during the holiday period.

Selection of drying techniques for Pingyin rose on the basis of physicochemical properties and volatile compounds retention

Awareness of edible rose being beneficial for health has attracted researchers in exploring different rose products. The study aimed to investigate effects of vacuum freeze drying (VFD), hot air drying (HAD), heat pump drying (HPD), relative humidity drying (RHD) and catalytic infrared drying (CID) on the physicochemical properties, and volatile organic compounds (VOCs) of Pingyin roses. Results showed that the VFD roses had significantly (p < 0.05) bright color, complete tissue cells, low shrinkage, and good plasma membrane permeability. CID roses showed the highest total phenols content (164.09 ± 0.88 mg/g) and the strongest antioxidant activity. Besides, the odor is the most crucial indicator for dried roses. VFD can well prevent the odor from diminishing/destroying and preserve the natural smell of rose. Thermal drying including HAD, HPD, RHD, and CID, could cause significant losses of VOCs. Consequently, the findings can provide the scientific basis for future large-scale production of dried rose products.

The impacts of VOCs on PM2.5 increasing via their chemical losses estimates: A case study in a typical industrial city of China

Volatile organic compounds (VOCs) have been explicitly required to be controlled by national or local governments to tackle heavy PM2.5 pollution in China. However, the role of VOCs chemistry in PM2.5 is still far away from being fully understood. In this study, we selected a typically industrialized city of China, conducted VOCs online measurements in July and December of 2020, estimated VOCs chemical losses, and explored their impacts on PM2.5 in the real atmosphere. Our measurements totally detected the mixing ratios of 53 VOCs species, sum of which reaching 20.8 ± 9.1 ppb and 45.5 ± 19.8 ppb in July and December respectively. Based on the change in the relative abundance of various VOCs species with different reactivity, daily OH exposure and daily O3 exposure (molecules·s·cm−3) were estimated, respectively with the mean value of 11.0 × 1010 and 5.2 × 1015 in July, 5.9 × 1010 and 3.1 × 1015 in December. Thus, there were about 6.7 ± 3.2 ppb and 11.1 ± 5.0 ppb VOCs chemically lost in July and December, with the average loss ratio of 29.7% and 19.3% in respective. In July, PM2.5 in the range of 20–60 μg m−3 positively responded to VOCs loss ratios, and high PM2.5 values were always accompanied by higher VOCs losses instead of high CO levels; but their relationship became negative in December when PM2.5 in the range of 40–150 μg m−3, and extremely high PM2.5 values happened in high CO conditions instead of high VOCs losses conditions. Moreover, PM2.5 measurements in this city also showed an apparent upward trend in OC/EC with PM2.5 in summer, but a slight downward trend in winter. These all indicated that in the conditions of stronger solar radiations (summer) and low-middle aerosol loads, VOCs chemistry played the important role in PM2.5 increasing through contributing SOA; but in the conditions of lower solar radiations (winter) and heavy aerosol loads, VOCs chemistry was greatly weakened and had the minor impact on PM2.5 increasing. The measure involving VOCs reduction to alleviate PM2.5 pollution in winter needs to be cautiously considered and examined.

Real-Time Laboratory Measurements of VOC Emissions, Removal Rates, and Byproduct Formation from Consumer-Grade Oxidation-Based Air Cleaners

Levels of volatile organic compounds (VOCs) in the indoor environment can be decreased by the use of “air cleaners”, devices that remove VOCs by sorption and/or oxidative degradation. However, efficacies of these technologies for removing VOCs tend to be poorly constrained, as does the formation of oxidation byproducts. Here, we examine the influence of several oxidation-based air cleaners, specifically ones marketed as consumer-grade products, on the amounts and composition of VOCs. Experiments were conducted in an environmental chamber, with a suite of real-time analytical instruments to measure direct emissions, VOC removal efficacies (by the addition of either limonene and toluene), and byproduct formation. We find that the air cleaners themselves can be a source of organic gases, that removal efficacy can be exceedingly variable, and that VOC loss is primarily driven by physical removal in some cleaners. When oxidative degradation of VOCs was observed, it was accompanied by the formation of a range of oxidation byproducts, including formaldehyde and other oxygenates. These results indicate that some consumer-grade portable air cleaners can be ineffective in removing VOCs and that the air delivered may contain a range of organic compounds, due to direct emission and/or byproduct formation.