Total Mass Concentration Research Articles

Two-in-one sensor of refractive index and Raman scattering using hollow−core microstructured optical waveguides for colloid characterization

Hollow−core microstructured optical waveguides (HC−MOW) have recently emerged in sensing technologies, including the gas and liquid detection for industrial as well as clinical applications. Antiresonant HC−MOW provide capabilities for applications in refractive index (RI) sensing, while the long optical path for analyte−light interaction in HC−MOW leads to increased sensitivity of sensor based on Raman scattering signal measurements. In this study, we developed a two−in−one sensor device using HC−MOW for RI and Raman scattering detection. The performance of the sensor was evaluated by characterizing protein−copolymer multicomponent colloids, specifically, bovine serum albumin (BSA) and poly(N − vinyl−2 −pyrrolidone−co−acrylic acid) P(VP−AA) nano−sized complexes and microbubbles of the corresponding shell. Monocomponent solutions showed linear dependencies of RI and characteristic Raman peak intensities on mass concentration. Multicomponent Raman sensing of BSA@P(VP−AA) complexes and microbubbles revealed that changes in P(VP−AA) characteristic peak intensities can describe interactions between components needed to produce colloid systems. RI sensing of multicomponent colloids demonstrated linear dependence on total mass concentrations for BSA@P(VP−AA) complexes, while corresponding BSA@P(VP−AA) microbubbles can be detected with concentrations as high as 4.0 × 108 MB/mL. Therefore, the developed two−in−one sensor of RI and Raman scattering can be used the robust characterization of albumin−based colloids designed for therapeutic and diagnostic needs.

Size-fractionated carbonaceous particles and climate effects in the eastern region of Myanmar

This study reports on an investigation of fine and coarse carbonaceous particulate matters (PM) in Tachileik, eastern Myanmar, during the dry and wet seasons of 2022. The carbon compositions, including organic carbon (OC) and elemental carbon (EC), in each size (PM10-2.5, PM2.5-1.0, and PM1.0-0.5) were determined by a carbon analyzer. The average total mass concentration of the three fractions of particle samples during the dry season was higher (51.23 ± 23.86 μg/m3) than that of the wet season (14.00 ± 5.26 μg/m3). The results indicate that OC and EC levels were highest for PM1.0-0.5 during the dry season and the sizes were similar for both seasons. The OC/EC ratios varied in different seasons, from 1.93 to 4.40 and 4.13 to 5.25 in the dry and wet seasons, respectively. EC was sub-divided into char-EC and soot-EC; the char-EC/soot-EC in the dry season was higher than in the wet season, signifying that biomass burning is the main particle source during the dry season. However, vehicle emissions dominated during the wet season. The effective carbon ratio (ECR) suggested that finer particles contributed more to global warming. This information is important in terms of air quality control and mitigation in Myanmar and elsewhere.

A promising approach to monitor microplastic masses in composts

Inputs of plastic impurities into the environment via the application of fertilizers are regulated in Germany and the EU by means of ordinances. Robust and fast analytical methods are the basis of legal regulations. Currently, only macro- and large microplastic contents (>1 mm) are measured. Microplastics (1–1,000 µm), are not yet monitored. Thermal analytical methods are suitable for this purpose, which can determine the mass content and can also be operated fully automatically in routine mode. Thermal extraction desorption-gas chromatography/mass spectrometry (TED-GC/MS) allows the identification of polymers and the determination of mass contents in solid samples from natural environments. In accordance with the German or European Commission (EC) Fertiliser Ordinance, composting plants should be monitored for microplastic particles with this method in the future. In this context a compost plant was sampled. At the end of the rotting process, the compost was sieved and separated in a coarse (>1 mm) and a fine fraction (<1 mm). The fine fraction was processed using density separation comparing NaCl and NaI as possible salt alternative and screened for microplastic masses by TED-GC/MS with additional validation and quality assurance experiments. With TED-GC/MS total microplastics mass contents of 1.1–3.0 μg/mg in finished compost could be detected with polyethylene mainly. What differs much to the total mass of plastics in the coarse fraction with up to 60 μg/mg, which were visually searched, identified via ATR-FTIR and gravimetrically weighted.

Mobile measurements for distribution and attribution of particulate matter in urban environments

Particulate matter (PM) sources differ in urban environments and may show spatiotemporal distinct patterns for varying particle aerodynamic diameters (DP). We here assess such patterns using high-resolution PM ≤10 μm data recorded with a cargo bike along a 14 km route through urban, suburban, and rural areas in Mainz (Germany). The measurements conducted twice a day between May and August 2021 reveal decreasing particle number concentration (PNC) with increasing DP including ∼6000 times higher particle numbers at DP 0.22–0.25 μm compared to DP 4–5 μm. Total mass concentration is bi-modally distributed and dominated by particles <0.3 μm and from 3 to 5 μm representing 36 and 22% of the entire air load, respectively. PM concentrations in Mainz are significantly higher in the morning than in the afternoon, and PM1 and PM10 are 13 and 31% higher in urban compared to surrounding suburban and rural areas. The high-resolution measurements also revealed 30% higher PM concentrations at DP 3–5 μm in the urban compared to the rural sectors, which is indicative for road dust, brake and tyre abrasion as the main source. DP distribution in rural hotspots is generally shifted toward larger particles >3 μm, most likely related to natural dust from agricultural fields. These findings show that high-resolution PM profiles can skillfully be recorded using bikes as mobile platform to identify spatial pollution patterns and attribute DP spectra to particular emission sources.

Relationship of cardiac remodeling and perfusion alteration with hepatic lipid metabolism in a prediabetic high fat high sucrose diet female rat model

Background and aimsCardiovascular disease (CVD) is known to be linked with metabolic associated fatty liver disease and type 2 diabetes, but few studies assessed this relationship in prediabetes, especially among women, who are at greater risk of CVD. We aimed to evaluate cardiac alterations and its relationship with hepatic lipid metabolism in prediabetic female rats submitted to high-fat-high-sucrose diet (HFS). Methods and resultsWistar female rats were divided into 2 groups fed for 5 months with standard or HFS diet. We analyzed cardiac morphology, function, perfusion and fibrosis by Magnetic Resonance Imaging. Hepatic lipid contents along with inflammation and lipid metabolism gene expression were assessed. Five months of HFS diet induced glucose intolerance (p < 0.05), cardiac remodeling characterized by increased left-ventricular volume, wall thickness and mass (p < 0.05). No significant differences were found in left-ventricular ejection fraction and cardiac fibrosis but increased myocardial perfusion (p < 0.01) and reduced cardiac index (p < 0.05) were shown. HFS diet induced hepatic lipid accumulation with increased total lipid mass (p < 0.001) and triglyceride contents (p < 0.05), but also increased mitochondrial (CPT1a, MCAD; (p < 0.001; p < 0.05) and peroxisomal (ACO, LCAD; (p < 0.05; p < 0.001) β-oxidation gene expression. Myocardial wall thickness and perfusion were correlated with hepatic β-oxidation genes expression. Furthermore, myocardial perfusion was also correlated with hepatic lipid content and glucose intolerance. ConclusionThis study brings new insights on the relationship between cardiac sub-clinical alterations and hepatic metabolism in female prediabetic rats. Further studies are warranted to explore its involvement in the higher CVD risk observed among prediabetic women.

Source apportionment of volatile organic compounds during paddy-residue burning season in north-west India reveals large pool of photochemically formed air toxics

Paddy-residue burning is associated with poor air quality in north-west India during October–November every year. However, till date a quantitative study of its contribution to ambient volatile organic compounds (VOCs) using highly time-resolved measurements within the region has been lacking. Several VOCs like benzene are carcinogenic and also fuel formation of secondary pollutants such as secondary organic aerosol (SOA) and ozone. Here, we undertake quantitative source-apportionment using a PMF source-receptor model on a high-quality in-situ measured dataset of 54 VOCs in Punjab, India, and validate the model results using source profiles. The contribution of the seven most dominant sources to the total VOC mass concentrations were: daytime photochemistry and biogenic VOCs (BVOCs) (26%), followed by solid-fuel usage and waste-disposal (18%), traffic (two-wheeler 14% and four-wheeler 10%), photochemically aged biomass burning (17%), industries and solvent usage (9%), and fresh paddy residue burning (6%). Ozone production potential was dominated by solid fuel usage and waste disposal (25%), followed by traffic (two-wheeler 11% and four-wheeler 12%), BVOCs and photooxidation products (21%), photochemically aged biomass burning (16%), industries & solvent usage (9%) and fresh paddy residue burning (6%). SOA production was dominated by traffic (two-wheeler 26% and four-wheeler 28%) followed by solid fuel usage and waste disposal (22%), photochemically aged biomass burning emissions (15%) with minor contribution from industries & solvents (6%), fresh paddy residue burning (2%) and photochemistry and biogenic VOCs (1%). Comparisons with global emission inventories REASv3.2.1 and EDGARv4.3.2, showed both overestimate the industry and solvent source. Further, EDGARv4.3.2 underestimated the traffic source whereas paddy residue burning emissions are absent in REASv3.2.1. Although the overall mass contribution of paddy-residue burning emissions isn't high, our results show that health-relevant compounds emitted directly and formed photochemically from biomass burning sources active at this time are majorly responsible for the unhealthy air.

AVALIAÇÃO DE PARÂMETROS RELACIONADOS A FIXAÇÃO BIOLÓGICA DE NITROGÊNIO EM SOJA cv. TMG 2165 IPRO PRÉ-COINOCULADA EM DIFERENTES MOMENTOS ANTES DA SEMEADURA

The objective was to evaluate parameters of biological nitrogen fixation in soybean subjected to different treatments: T1 - control without the use of commercial inoculant; T2 - chemical nitrogen fertilization; T3 - commercial inoculant based Bradyrhizobium applied to the seeds on the sowing day; use of commercial inoculant containing Bradyrhizobium and Azospirillum bacteria applied at 0, 7 and 15 days before sowing (DBS), treatments T4, T5 e T6, respectively. In R2, the following parameters were evaluated: number of nodules and dry mass in the main root, secondary roots and total; shoot and total dry mass and nitrogen content in the soot (NCS). In R8, the accumulated nitrogen content in the grains (NCG) was measured. From the results obtained, it can be noted that for the nodulation parameters (nodular number and dry mass) the treatments that stood out were related to co-inoculation (T4, T5 e T6) without statistical difference regarding the period of application of the inoculant. With regard to NCS, there was a greater increase in treatments T4 and T2, which did not differ from each other and presented mean values of 33.84 and 33.23 kg ha-1, respectively. For NCG, T4 stood out with 58.43 kg ha-1, despite having statistical similarity to treatments that used the same inoculant applied to 7 (T5) and (T6) DBS, as well as T2 and T3. It can be concluded that the parameters to biological nitrogen fixation did not suffer a negative influence due to the application of early co-inoculation up to 15 days before soybean sowing.

Long-term trends in inorganic aerosol chemical composition and chemistry at an urban and rural site in the northeastern US

Atmospheric nitrate and sulfate are major inorganic particulate matter components that impact human and ecosystem health and air quality. Over the last several decades, emissions of the precursor gases, nitrogen oxides (NOx = NO + NO2) and sulfur dioxide (SO2), have dramatically decreased in the US in response to federal regulations. However, the response in concentrations of particulate nitrate (pNO3) and sulfate (pSO4) have not followed predictions due to complex non-linear chemistry feedbacks that may differ amongst environments (i.e., urban vs. rural). In this study, we explored the long-term response of particle chemistry for urban and rural environments in southern New England, a region historically impacted by NOx and SO2 emissions. Particulate matter (PM10) samples collected via the same method from 2005 to 2015 at urban and rural locations in Rhode Island were analyzed for their major inorganic components, and air mass trajectories and statistical analysis were used to identify source regions over time. Our results indicated a significant urban-rural aerosol chemical composition gradient for sampling locations within 40 km. Over time, as anthropogenic influences have decreased, the relative contribution of marine and crustal sources has increased greatly, impacting fine and coarse particle chemistry in recent years. Total mass concentrations of chemical species, particularly anthropogenic pSO4 and particulate ammonium (pNH4), have shown dramatic decreases over the ten years at both the urban and rural sites; however, pNO3 concentration increased by 95 % and 57 % in the urban and rural sites, respectively, despite significant NOx emission reductions. Our results demonstrate that changes in chemical mechanisms due to the decrease in SO2 emissions contributed to decreases in pNH4, along with enhanced pNO3 concentration. Furthermore, the change in SO2 emissions has significantly impacted the atmospheric lifetime and transport distance of pNH4, favoring more localized contributions in recent years.

Climatology of aerosol properties at an atmospheric monitoring site on the northern California coast

Abstract. Between April 2002 and June 2017, the Global Monitoring Laboratory (GML) of the National Oceanic and Atmospheric Administration (NOAA) made continuous measurements of a suite of in situ aerosol optical properties at a long-term monitoring site near Trinidad Head (THD), California. In addition to aerosol optical properties, between 2002–2006 a scanning humidograph system was operated, and inorganic ion and total aerosol mass concentrations were obtained from filter measurements. A combined analysis of these datasets demonstrates consistent patterns in aerosol climatology and highlights changes in sources throughout the year. THD is predictably dominated by sea salt aerosols; however, marine biogenic aerosols are the largest contributor to PM1 in the warmer months. Additionally, a persistent combustion source appears in the winter, likely a result of wintertime home heating. While the influences of local anthropogenic sources from vehicular and marine traffic are visible in the optical aerosol data, their influence is largely dictated by the wind direction at the site. Comparison of the THD aerosol climatology to that reported for other marine sites shows that the location is representative of clean marine measurements, even with the periodic influence of anthropogenic sources.

Road dust resuspension in a coastal Atlantic intermunicipal urban area with industrial facilities: Emission factors, chemical composition and ecotoxicity

Road dust resuspension in urban environments can be both a means of transport of pollutants across the various environmental compartments and a source of pollutants itself, becoming a potential threat to human health. With the aim of obtaining emission factors and achieving a detailed chemical characterisation of road dust (RD) in typical Portuguese cities, a sampling campaign was performed in the region of Aveiro. Locations were chosen for intercomparison in various urban environments with different land uses, from the busier city centre and university campus to residential neighbourhoods and harbour-commercial areas with industrial activities. PM10 samples were analysed for organic and elemental carbon (OC and EC) by a thermal-optical technique, elemental composition by PIXE, organic speciation by GC–MS, and ecotoxicology by a luminescence inhibition bioassay with Aliivibrio fischeri. A health risk assessment for elements and PAHs was carried out. Dust loadings of 1.9 ± 1.8 mg PM10 m−2 were registered overall, whereas in the most trafficked areas of city centre they reached more than three times the average. OC accounted for 6.5–15.5% of total PM10, but element oxides represented the largest mass fraction (61.4 ± 8.6%). A strong enrichment was detected mostly for typical traffic-related elements such as Cu, Zn, As, Br, Cr, Ni and Mo and interestingly, Rb and Se. The analysed organic compounds accounted for 3.66–11.0 mg g−1 PM10, including PAHs and aliphatics, with a clear dominance of plasticisers. Some other compounds attributed to non-vehicle sources, such as fatty acid alkyl esters, were also detected. As concerns the 16 priority PAHs, their total mass concentration ranged from 5.58 to 36.3 μg g−1 PM10, with clear variability between sampling spots. All samples caused an ecotoxicological reaction in the bioassay, but samples from harbour and commercial areas proved to be most toxic.

Short-chain fatty acids facilitated long-term dechlorination of PCBs in Taihu Lake sediment microcosms: Evidence from PCB congener and microbial community analyses

Microbial reductive dechlorination hosts great promise as an in situ bioremediation strategy for polychlorinated biphenyls (PCBs) contamination. However, the slow dechlorination in sediments limits natural attenuation. Short-chain fatty acids, as preferred carbon sources and electron donors for dechlorinating microorganisms, might stimulate PCB dechlorination. Herein, two sets of short-chain fatty acids, sole acetate and a fatty acid mixture (acetate, propionate, and butyrate), were amended periodically into Taihu Lake (China) sediment microcosms containing nine PCB congeners (PCB5, 12, 64, 71, 105, 114, 149, 153, and 170) after 24 weeks of incubation. Short-chain fatty acids facilitated the long-term PCB dechlorination and the promoting effect of the fatty acid mixture compared favorably with that of sole acetate. By the end of 108 weeks, the total PCB mass concentrations in acetate amended and fatty acid mixture amended microcosms significantly declined by 7.6% and 10.3% compared with non-amended microcosms (P < 0.05), respectively. Short-chain fatty acids selectively favored the removal of flanked meta and single-flanked para chlorines. Notably, a rare ortho dechlorination pathway, PCB25 (24-3-CB) to PCB13 (3-4-CB), was enhanced. Supplementary fatty acids significantly increased reductive dehalogenases (RDase) gene pcbA5 instead of improving the growth of Dehalococcoides. These findings highlight the merits of low cost short-chain fatty acids on in situ biostimulation in treating PCBs contamination.

Atmospheric Oxidation Capacity and Its Impact on the Secondary Inorganic Components of PM2.5 in Recent Years in Beijing: Enlightenment for PM2.5 Pollution Control in the Future

In recent years, the concentrations of PM2.5 in urban ambient air in China have been declining; however, the strong atmospheric oxidation capacity (AOC) represents challenges to the further reduction of PM2.5 concentration and the continuous improvement of ambient air quality in China in the future, since the overall AOC is still at a high level. For this paper, based on ground observation data recorded in Beijing from 2016 to 2019, the variation in AOC was characterized according to the concentration of odd oxygen (OX = O3 + NO2). The concentrations of the primary and secondary components of PM2.5 were analyzed using empirical formulas, the correlation between AOC and the concentrations of secondary PM2.5 and the secondary inorganic components (SO42−, NO3−, NH4+, and SNA) in Beijing were explored, the impact of atmospheric photochemical reaction activity on the generation of atmospheric secondary particles was evaluated, and the impact of atmospheric oxidation variations on PM2.5 concentrations and SNA in Beijing was investigated. The results revealed that OX concentrations reached their peak in 2016 and reached their lowest point in 2019. The OX concentrations followed a descending seasonal trend of summer, spring, autumn, and winter, along with a spatial descending trend from urban observation stations to suburban stations and background stations. The degree of photochemical activity and the magnitude of the AOC have a large influence on the production of atmospheric secondary particles. When the photochemical reaction was more active and the AOC was stronger, the mass concentrations of the secondary generated PM2.5 fraction were higher and accounted for a higher proportion of the total PM2.5 mass concentrations. In the PM2.5 fraction, SNA accounted for 50.7% to 94.4% of the total mass concentrations of water-soluble inorganic ions in the field observations. Higher concentrations of the atmospheric oxidant OX in ambient air corresponded to a higher sulfur oxidation ratio (SOR) and nitrogen oxidation ratio (NOR), suggesting that the increase in AOC could promote the increase of PM2.5 concentration. Based on a relationship analysis of SOR, NOR, and OX, it was inferred that the relationship between OX and SOR and the relationship between OX and NOR were both nonlinear. Therefore, when establishing PM2.5 control strategies in Beijing in the future, the impact of the AOC on PM2.5 generation should be fully considered, and favorable measures should be taken to properly regulate the AOC, which would be more effective when carrying out further control measures regarding PM2.5 pollution.

Characterization of size-differentiated airborne particulate matter collected from indoor environments of childcare facilities

Inhalation of particulate matter (PM) present in indoor atmospheres has been associated with poor health and wellbeing of occupants. Here we report the characteristics of airborne PM collected from twenty-two air-conditioned childcare centres in Singapore. Airborne PM were collected using cascade impactors and characterized for morphology, elemental composition, endotoxin levels, ability to generate abiotic reactive oxygen species, and oxidative stress-dependent cytotoxicity in BEAS-2B cell lines. The mass concentrations of ultrafine particles (PM0.06-1) were more abundant than that of larger particles (PM1-4, PM4-20, and PM20-35 particles). PM20-35 and PM4-20 were irregularly shaped particles, PM1-4 particles had membranous flaky structures and PM0.06-1 particles were pseudo-spherical with the occasional presence of crystalline structures. Carbonaceous matter dominated PM20-35 particles, and the abundance of inorganic salts, iron and sulfur increased with decreasing PM size. Measured endotoxin levels were especially higher in PM4-20 particles. Compared to other particle size fractions, PM0.06-1 particles generated the highest ROS and were also the most potent in generating intracellular ROS in BEAS-2B cell lines. However, total mass concentrations, elemental compositions, abiotic responses, and PM collected from centres with split air-conditioning systems and no active outdoor air supply (SAC) were not statistically different compared with PM collected from centres with air conditioning with mechanical ventilation (ACMV). In conclusion, our study showed obvious distinctions in mass concentrations, morphology, elemental compositions, and cytotoxic potential of different sized particles collected from childcare centres, where the smallest particles (PM0.06-1) exhibited higher hazard potential.

How Important Is Satellite-Retrieved Aerosol Optical Depth in Deriving Surface PM2.5 Using Machine Learning?

PM2.5 refers to the total mass concentration of tiny particulates in the atmosphere near the surface, obtained by means of in situ observations and satellite remote sensing. Given the highly limited number of ground observation stations of inhomogeneous distribution and an ill-posed remote sensing approach, increasing efforts have been devoted to the application of machine-learning (ML) models to both ground and satellite data. A key satellite-derived parameter, aerosol optical thickness (AOD), has been most commonly used as a proxy of PM2.5, although their correlation is fraught with large uncertainties. A critical question that has been overlooked concerns how much AOD helps to improve the retrieval of PM2.5 relative to its uncertainty incurred concurrently. The question is addressed here by taking advantage of high-density PM2.5 stations in eastern China to evaluate the contributions of AOD, determined as the difference in the accuracy of PM2.5 retrievals with and without AOD for varying densities of PM2.5 stations, using four popular ML models (i.e., Random Forest, Extra-trees, XGBoost, and LightGBM). Our results reveal that as the density of monitoring stations decreases, both the feature importance and permutation importance of satellite AOD demonstrate a consistent upward trend (p &lt; 0.05). Furthermore, the ML models without AOD exhibit faster declines in overall accuracy and predictive ability compared with the models with AOD assessed using the sample-based and station-based (spatial) independent cross-validation approaches. Overall, a 10% reduction in the number of stations results in an increase of 0.7–1.2% and 0.6–1.2% in uncertainty in estimated and predicted accuracies, respectively. These findings attest to the indispensable role of satellite AOD in the PM2.5 retrieval process through ML because it can significantly mitigate the negative impact of the sparse distribution of monitoring sites. This role becomes more important as the number of PM2.5 stations decreases.

Abundance, Distribution, and Characterization of Microplastics on Two Recreational Beaches in Kota Kinabalu, Sabah, Malaysia

Currently, there is a lack of assessment of the level of microplastics (MPs) pollution on recreational beaches around the world. Therefore, this study was conducted to determine the current state of MP pollution on two popular recreational beaches of Kota Kinabalu, Sabah, namely, (1) Tanjung Aru Beach and (2) UMS ODEC (Outdoor Development Center) beach. MPs from the sediments were extracted using the density separation method and analyzed through a stereoscopic microscope. The overall MPs abundance, weight, size, colors, and polymer types were recorded. Tanjung Aru beach recovered higher numbers of MPs particles for all stations, with 857 MPs/kg dry sediment with a total mass concentration of 57.72 g/kg, while UMS ODEC recorded 160 MPs/kg particles with a total mass concentration of 17.96 g/kg. The maximum MPs abundance was observed in the size of &lt;1 mm with a high proportion of white/transparent coloring. Micro Fourier Transform Infrared Spectroscopy (FTIR) analysis revealed that polypropylene (PP:60%) and polyethylene (PE:43%) were the two most common plastic polymers found on both beaches, followed by polyethylene terephthalate (PET), and the least common was polystyrene (PS). Metals (arsenic, chromium, copper, and nickel) were found within the MPs collected. The present study demonstrated an alarming quantity of MPs on two recreational beaches in Kota Kinabalu, Sabah, Malaysia. However, information concerning the primary sources, local dynamics, and repercussions of MPs in this location is still limited; thus, further research is required.

Spatial distributions of PM10-bound metal elements in the central part of western Taiwan and their potential emission sources and the carcinogenic health risks.

This study aimed to investigate the spatial distribution of metal elements in PM10 and their potential sources and associated health risks over a period of two years in eight locations in the central part of western Taiwan. The study revealed that the mass concentration of PM10 and the total mass concentration of 20 metal elements in PM10 were 39.0 μg m-3 and 4.74 μg m-3, respectively, with total metal elements accounting for approximately 13.0% of PM10. Of the total metal elements, 95.6% were crustal elements (Al, Ca, Fe, K, Mg, and Na), with trace elements (As, Ba, Cd, Cr, Co, Cu, Ga, Mn, Ni, Pb, Sb, Se, V, and Zn) contributing only 4.4%. Spatially, the inland areas exhibited higher PM10 concentrations due to lee-side topography and low wind speeds. In contrast, the coastal regions exhibited higher total metal concentrations because of the dominance of crustal elements from sea salt and crustal soil. Four primary sources of metal elements in PM10 were identified as sea salt (58%), re-suspended dust (32%), vehicle emissions and waste incineration (8%), and industrial emissions and power plants (2%). The positive matrix factorization (PMF) analysis results indicated that natural sources like sea salt and road dust contributed up to 90% of the total metal elements in PM10, while only 10% was attributed to human activities. The excess cancer risks (ECRs) associated with As, Co, and Cr(VI) were greater than 1 × 10-6, and the total ECR was 6.42 × 10-5. Although only 10% of total metal elements in PM10 came from human activities, they contributed to 82% of the total ECR.

The variability of mass concentrations and source apportionment analysis of equivalent black carbon across urban Europe

This study analyzed the variability of equivalent black carbon (eBC) mass concentrations and their sources in urban Europe to provide insights into the use of eBC as an advanced air quality (AQ) parameter for AQ standards. This study compiled eBC mass concentration datasets covering the period between 2006 and 2022 from 50 measurement stations, including 23 urban background (UB), 18 traffic (TR), 7 suburban (SUB), and 2 regional background (RB) sites. The results highlighted the need for the harmonization of eBC measurements to allow for direct comparisons between eBC mass concentrations measured across urban Europe. The eBC mass concentrations exhibited a decreasing trend as follows: TR > UB > SUB > RB. Furthermore, a clear decreasing trend in eBC concentrations was observed in the UB sites moving from Southern to Northern Europe. The eBC mass concentrations exhibited significant spatiotemporal heterogeneity, including marked differences in eBC mass concentration and variable contributions of pollution sources to bulk eBC between different cities. Seasonal patterns in eBC concentrations were also evident, with higher winter concentrations observed in a large proportion of cities, especially at UB and SUB sites. The contribution of eBC from fossil fuel combustion, mostly traffic (eBCT) was higher than that of residential and commercial sources (eBCRC) in all European sites studied. Nevertheless, eBCRC still had a substantial contribution to total eBC mass concentrations at a majority of the sites. eBC trend analysis revealed decreasing trends for eBCT over the last decade, while eBCRC remained relatively constant or even increased slightly in some cities.

Comprehensive study on particle size distribution, MAH and PAH profiles during alkylbenzene pyrolysis

The 5 linear alkylbenzenes, i.e., toluene, ethylbenzene, n-propylbenzene, n-butylbenzene, and n-pentylbenzene as fuels underwent pyrolysis at temperatures from 950 to 1450 °C in a flow reactor. Measurements of particle number size distribution, 11 monocyclic aromatic hydrocarbons, and 3 groups of polycyclic aromatic hydrocarbons (20 unsubstituted PAHs, 5 aliphatic-bridged PAHs, and 10 methyl PAHs) during the pyrolysis of linear alkylbenzenes were conducted. Results showed that the increase in side chain length suppressed the formation of particles, but ethylbenzene produced the highest particle mass and most extensive particle number size distribution. Total particle peak number concentrations exhibited a rise-then-fall trend (peaking at a critical temperature of 1050 °C) with increasing temperature regardless of the side chain length, indicating that high temperature promoted a transition from nucleation to agglomeration and coagulation. Total PAH mass concentrations were ranked in the same order with the variation of side-chain length as particle mass and peak number concentrations, indicating that soot nucleation was highly related to total PAH mass concentrations. Unsubstituted PAHs accounted for most PAHs while substituted·PAHs, including aliphatic-bridged PAHs and methyl PAHs presented 1–2 orders of magnitude less than the corresponding unsubstituted PAHs, probably distinct thermal stability and reactivity led to different growth routes between unsubstituted and substituted PAHs. Increasing the temperature from 950 to 1250 °C, the formation of high molecular weight PAHs was promoted. while a drop of high molecular weight fractions was observed above 1350 °C, which is attributed to the suppression of the formation, as well as their conversions of high molecular weight PAHs to heavier unidentified PAHs or soot. Among the test alkylbenzene fuels, the fuels with a long side chain benefit from the reduction of particles and PAHs. Furthermore, carbon atoms in aromatic rings are dominant sources of large PAHs and particles, while the carbon atoms in aliphatic side chains mainly form gas species.

Degradation of Methylene Blue Dye in Wastewater Using Ozonation Method with H2O2 Catalyst

Water pollution is still a serious problem in Indonesia. One of the pollutants that contribute to water pollution is dye. One type of dye that is often used in the textile industry is methylene blue. There are several methods for treating dye waste, one of which is the ozonation method. Ozonation is a chemical oxidation process to remove the color of organic dyes. The catalytic ozonation process can increase the ability of ozone in sewage treatment. The catalyst used is H2O2 which can decompose into OH radicals. OH radicals have a higher reduction potential than other oxidizing agents. Ozonation research with H2O2 catalyst aims to determine changes in the concentration of dyes, COD and BOD5. In testing the ozonation time (0.15,30,45,60) minutes, the pH conditions (5,7,9) and the total mass concentration of H2O2 (0.2,5,5,7,5,10) % showed that the longer the time ozonation, the higher the pH value. and the more H2O2 used, the less concentration of dye, COD and BOD5.

Sources, size-resolved deposition in the human respiratory tract and health risks of submicron black carbon in urban atmosphere in Pearl River Delta, China

Black carbon (BC) has a significantly negative impact on air quality, climate and human health. Here we investigated the sources and health effects of BC in urban area of the Pearl River Delta (PRD) based on online data measured by Aerodyne soot particle high-resolution time of flight aerosol mass spectrometer (SP-AMS). In urban PRD, BC particles mainly came from vehicle emissions especially heavy-duty vehicle exhausts (contributing 42.9 % of total BC mass concentration), long-range transport (27.6 %), and aged biomass combustion emissions (22.3 %). Indicated by source analysis using simultaneous aethalometer data, BC associated with local secondary oxidation and transport may also be originated from fossil fuel combustion, especially traffic sources in urban and surrounding areas. Size-resolved BC mass concentrations provided by SP-AMS, for the first time to our best knowledge, were used to calculate BC deposition in the human respiratory tract (HRT) of different populations (children, adults, and the elderly) by the Multiple-Path Particle Dosimetry (MPPD) model. We found that submicron BC was deposited more in the pulmonary (P) region (49.0–53.2 % of the total BC deposition dose), while less in the tracheobronchial (TB, 35.6–37.2 %) and head (HA, 11.2–13.8 %) regions. Adults suffered the highest BC deposition (1.19 μg day−1) than the elderly (1.09 μg day−1) and children (0.25 μg day−1). BC deposition rate was greater at night (especially 18:00–24:00) than during the daytime. The maximum deposition in the HRT was found for BC particles around 100 nm, mainly in deeper respiratory regions (TB and P), which may cause more serious health effects. Adults and the elderly group are confronted with the notable carcinogenic risk of BC in the urban PRD, up to 29 times higher than the threshold. Our study emphasizes the need to control BC pollution in the urban area, especially nighttime vehicle emissions.