Pyrene Concentration Research Articles

Air quality and the risk of acute atrial fibrillation (EP-PARTICLES study): A nationwide study in Poland.

Air pollution remains the single largest environmental health risk factor, while atrial fibrillation (AF) is the most prevalent arrhythmia globally. The study aimed to investigate the relationship between short-term exposure to air pollution and acute AF admissions. Individual data on AF hospitalization in the years 2011-2020 were collected from the National Health Fund in Poland (ICD-10: I48.XX). To obtain high-resolution data on air pollution we applied a modelling method using the GEM-AQ model. Associations between air pollution exposure and acute AF admissions were estimated using generalized additive models with Poisson regression. Over the analysed period, we recorded 252,566 acute admissions due to AF. Each 10 µg/m3 increment of PM2.5 and NO2 concentration, 1 µg/m3 of SO2 and 10 ng/m3 of benzo(a)pyrene (BaP) concentration on the day of exposure resulted in 1.13% (0.70%-1.55%), 1.65% (1.05%-2.26%), 0.11% (0.01%-0.21%), and 0.3% (0.04%-0.55%) increases in acute AF admissions, respectively. The estimates are larger for women and older people. Stronger associations between PM2.5 and BaP concentrations and AF admissions in poorly urbanized areas were noted. Areas with high gross domestic product levels were more affected by the increase in NO2 concentrations, resulting in a 0.2% (1.001-1.003) increase in AF admissions. Exposure-response functions show steeper slopes of the pollutant-outcome associations in the lower ranges of exposures, far below World Health Organization (WHO) air quality guideline norms. For the zero-emission scenario, we estimate avoidable AF admissions - 5,873 for PM2.5 (95% CI 3,679 to 8,047) and 3,295 for NO2 (2,108-4,477). Air pollution acts as a triggering factor and can be associated with acute AF hospitalisations. PM2.5 and NO2 have an impact on AF even at concentrations levels below WHO air quality guideline norms.

Understanding the Molecular Mechanisms of Pyrene in Governing the Critical Metabolic Circuits of Alexandrium pacificum.

Pyrene, a representative polycyclic aromatic hydrocarbon, frequently occurs in aquatic environments and is associated with lethal impacts on humans and wildlife. This study examined the impact of pyrene on Alexandrium pacificum, a dinoflagellate responsible for harmful algal blooms, and their capability to bioremove pyrene. In a 96 h exposure experiment, A. pacificum effectively reduced the pyrene concentration in seawater to 50, 100, and 200 μg/L, with a combined removal efficiency of 96% in seawater. Furthermore, the study noted a significant reduction in the synthesis of GTX4, GTX1, NEO, and GTX3 toxins in A. pacificum cells exposed to 50 and 200 μg/L of pyrene. Concurrently, exposure to pyrene resulted in marked declines in the growth and photosynthetic efficiency of A. pacificum. Proteomics analysis results showed an upregulation of proteins related to endocytosis, such as HSPA and Arf, while proteins associated with paralytic shellfish toxin (PST) synthesis, specifically SxtU and SxtH, showed a downregulation trend. In summary, the findings of this study preliminarily elucidate the molecular mechanisms underlying A. pacificum's response to pyrene, reveal the impact of pyrene on PST synthesis, and suggest that A. pacificum holds significant potential for pyrene biodegradation.

Influence of smoking method and anatomical location on the content of polycyclic aromatic hydrocarbons in Turopolje ham

In order to support a more sustainable breeding of the local Turopolje pig, the breed needs to be valorised through high added-value meat products, such as dry-cured and smoked Turopolje ham. To date, there are very few data on the quality and safety of Turopolje ham, including information on the content and distribution of potential contaminants such as polycyclic aromatic hydrocarbons (PAHs) from smoke. Hence, the aim of this study was to investigate the influence of smoking method (traditional or industrial) and anatomical site (M. biceps femoris - BF or M. semimembranosus - SM) on the content of PAHs in Turopolje ham. All hams (n=15) were produced the same way, differing only in smoking procedures; a traditional way above the firebox (group TRAD, n=5) or in the smoking chamber (group IND A - standard smoking, n=5 or B – 50 % reduced smoking, n=5). PAHs content (μg/kg) was determined and quantified by high-performance liquid chromatography with fluorescence detection (HPLC-FLD). Two-way analysis of variance was performed (GLM procedure of SAS) with fixed effects of smoking (S), muscle (M) and their interaction (SxM). Of the PAHs investigated, 14 compounds were detected. The results showed that TRAD hams had higher levels of anthracene (Ant), chrysene (Chr), benzo[b]fluoranthene (BbFA), benzo[a]pyrene (BaP), and the sum of benz[a]anthracene (BaA), Chr, BbFA and BaP (PAH 4) than hams from both A and B IND groups. TRAD hams had also higher content of acenaphthene (Acp), phenanthrene (Phen), pyrene (Py), BaA, and total PAHs than IND B hams. Compared to BF, SM muscle had higher content of several PAHs i.e. naphthalene (Nap), fluorine (Flu), Acp, Phen, Ant, fluoranthene (Flt), Py, BaA, benzo[k]fluoranthene (BkFA), benzo[ghi]perylene (BghiP), and also higher total PAH content. However, a significant SxM interaction was observed for Phen and Ant content which were higher only in SM muscle of TRAD hams. In conclusion, this study shows a marked influence of smoking method and anatomical site on the PAHs content in Turopolje hams, mainly in the form of lower BaP and the sum of PAH4 content in all chamber smoked hams compared to traditionally smoked hams and higher levels of light PAHs, some heavy PAHs and total PAH content in the more exposed SM compared to the inner BF muscle. Reduced smoking in IND hams did not affect BaP and the sum of PAH4 content, but reduced the content of some individual and total PAHs content. All IND hams and TRAD hams were below the maximum permitted level for BaP. However, two out of five hams from the TRAD group exceeded the limit for the sum of PAH4 (30 μg/kg) set by EU legislation for traditionally smoked meat products, indicating the need for stricter control of the traditional smoking process.

Can the agrochemical Oryzemate treatment control the uptake of pyrene by Cucurbita pepo through the regulation of major latex-like proteins?

Members of the Cucurbitaceae family accumulate several hydrophobic organic pollutants in their above-ground parts at high concentrations. Major latex-like proteins (MLPs) identified in Cucurbita pepo bind to hydrophobic organic pollutants, such as pyrene and dieldrin, in roots, forming complexes that are transported via xylem vessels to the above-ground plant parts. However, soil remediation of hydrophobic organic pollutants utilizing MLPs has not been established. In this study, the uptake of the hydrophobic organic pollutant pyrene by C. pepo was promoted through the upregulation of the expression of MLP genes following agrochemical treatment. Probenazole, an active ingredient in the agrochemical Oryzemate, was previously found to upregulate the promoter activity of MLP genes in the roots of transgenic tobacco plants. Here, Oryzemate treatment increased the levels of MLPs in the roots and xylem sap of C. pepo. Oryzemate treatment slightly increased and significantly decreased the pyrene concentration in the xylem sap of C. pepo cultivated in high- and low-contamination soils, respectively. Probenazole competitively inhibited the binding of MLPs to pyrene in vitro, thereby likely suppressing its uptake by C. pepo in low-contamination soil. This study demonstrated that Oryzemate possesses dual effects: effective phytoremediation and safe crop production, depending on the soil contamination level.

Removal of pyrene from domestic water supply using styrene-based imprinted polymer

Pyrene removal from domestic water supply (DWS) is important due to its mutagenicity, toxicity, and carcinogenicity. Use of molecularly imprinted polymer for pyrene removal is scarce, therefore the study developed polystyrene to complement conventional water treatment methods for pyrene removal. Bulk polymerisation was used to synthesise Pyrene imprinted polystyrene (PIP) and its non-imprinted analogue (NIP). Monoliths were characterised using SEM–EDX, FT-IR, and XRD. Extraction and concentration of pyrene were determined using GC–MS. Adsorption experiments on simulated solutions of pyrene with different concentrations, pH, adsorbent dosage, time, and temperature using PIP and NIP with equilibrium studies were done. Recovery was performed, while pyrene was adsorbed using simulated experiment best conditions. Used PIP and NIP were characterised. Pre-adsorption characterisation confirmed PIP and NIP while post-adsorption showed a clogged surface for NIP, but PIP was pyrene-selective. Pyrene concentration (0.05 mg/L) in DWS was > WHO standard (0.0002 mg/L) with 100% recovery. Adsorption efficiencies ranged from 25–100% and 15–100% with varied parameters for PIP and NIP respectively. However, best adsorption conditions are pH-9, time-1 h, adsorbent dosage-0.8 g, concentration-0.001 mgL−1, and temperature-27 °C with ΔG° (KJmol−1)13.48, 13.70, 13.94 for NIP and 21.24, 21.60, 21.95 for PIP. NIP ΔH° -0.3233 KJmol−1 and ΔS, 0.046 KJmol−1 k−1, while PIP ΔH° -0.0717KJmol−1 and ΔS, 0.071 KJmol−1 k−1. Adsorption fits Langmuir isotherm compared to others with R2 of 0.9140 and 0.9540 for PIP and NIP respectively. The study showed that both PIP and NIP removed pyrene from DWS with excellent efficiencies. However, PIP showed greater selectivity for pyrene removal.Graphical

Causes of the unremitting high ambient levels of PM10 in a suburban background site in NE Spain

Atmospheric PM10 and benzo(a)pyrene (BaP) concentrations in Manlleu (NE Spain) have remained high from 2008 to 2023, frequently exceeding EU limit/target values, and reaching BaP levels up to six times higher than urban averages in Spain. Furthermore, PM speciation campaigns were carried out in 2013, 2014–2015, 2016–2017 and 2021–2022. Chemical mass closure for autumn-winter showed a consistent PM10 composition for the different PM speciation campaigns, comprising 46–53% organic matter (OM), 18–26% secondary inorganic aerosol (SIA), 13–23% mineral matter (MM), and 5–9% elemental carbon (EC). Trend analysis revealed very light decrease and constant concentrations for PM10 and BaP, respectively over the study period, emphasizing the need for compliance with current and forthcoming EU air quality directives, the last aiming to halve PM10 limit values. Source apportionment of samples of the sporadic campaigns identified biomass burning (BB, 17.5 μg m−3, 48%) and MM and industry (16.3 μg m−3, 44%) as the main autumn-winter PM10 contributors, with high SIA concentrations attributed to several factors, including high ammonia (NH3) emissions. Local topography and meteorological conditions contribute to aggravate PM10 pollution. While metal concentrations have decreased since 2013, suggesting reduced industrial emissions, persistently high OM and EC concentrations indicate ongoing issues with BB emissions from domestic, commercial, and agricultural sources. Online analysis of black carbon (BC) and non-refractory PM1 components during winter 2016–2017 confirmed domestic and commercial BB as the primary sources of the BB contributions. These findings highlight the need of the implementation of more effective measures in reducing BB and agricultural/farming NH3 emissions. This study highlights the relevance of these issues for similar towns, the probable unremitting problem over the last decade, and the necessity of enhanced monitoring in small cities and policy actions to meet air quality standards under the new EU directive.

POLYCYCLIC AROMATIC HYDROCARBONS AS INDICATORS OF SOIL POLLUTION IN THE ZONE AFFECTED BY THE TRANSPORT COMMUNICATIONS OF THE GORLOVO ANTHRACITE DEPOSIT

The areas adjacent to open coal mining facilities are affected by different kinds of anthropogenic impact, including dust pollution. To reveal the extent of technogenic impact, the parameters characterising the content and composition of 19 priority polycyclic aromatic hydrocarbons (PAHs) in chernozem soils adjacent to the haul road of the Gorlovo anthracite deposit (the Novosibirsk Region) were assessed. It is shown that the maximum total concentration of PAHs (>1000 ng/g) is reached at the distance of 100 m from the source, while the levels higher than the background are detected at a distance of 1000 m. The effect of dominating wind direction and the presence of tree belt were determined to affect the total PAH content in soil but leave their group composition unchanged at a distance of 2000 m from the road. At the same time, the individual composition of PAHs in soils changes with an increase in the distance from the pollution source. The concentration of benz(α)pyrene and total PAH content, calculated for benz(α)pyrene toxic equivalents, were determined in the soils of territories adjacent to the road and compared with the current standards in force in the Russian Federation (sanitary rules and regulations). Statistical processing of the results, performed by the principal component analysis, shows that the input of black carbon in the form of anthracite coal dust into soil is most adequately represented by polyarene ratio PHE/(PHE + CHR), where PHE is phenanthrene, and CHR is chrysene. However, the threshold of technogenic load (<0.8), that was previously established for objects in which anthracite is the main source of PAHs, requires confirmation for black soils.

Pyrene Funtionlized Hollow Porous Carbon/S-Dib Composite As a Cathode for Lithium-Sulfur Batteries

Lithium-sulfur batteries (LiSBs) stand out as promising candidates for the next-generation energy storage system. However, challenges such as the “shuttling effects” of intermediate lithium polysulfides and sluggish conversion between sulfur and lithium sulfide have led to low specific capacity under high current and a shortened cycling life for LiSBs. Extensive research has explored porous carbon materials as hosts for sulfur in LiSBs cathodes. Nevertheless, overcoming the “shuttling effects” and ensuring the uniform deposition of lithium sulfide without using metals or metal-containing species remains a challenge.Taking advantage of its aromatic properties, which promotes robust π-π interactions with sp2-hybridized carbon, pyrene with various functionalized groups emerges as a viable solution for surface modification through non-covalent bonding to carbon. In this study, we present the synthesis of X-pyrene (X=OH, NH2, Cl) modified hollow porous carbon (HPC) serving as a micro-reactor for inverse vulcanization, resulting in the formation of S-DIB/X-HPC (X=OH, NH2, Cl) with a uniform structure. Abundant oxygen-, nitrogen- and chloride interfaces were designed to act as adsorption catalytic sites, accelerating conversion kinetics and mitigating shuttle effects.Hollow porous carbon (HPC) nanoparticles were prepared from ZIF-8 by carbonization at 950 °C under argon atmosphere. (Figure 1a). The cross-sectional view in Figure 1b reveals numerous individual hexagonal structures with abundant internal pores. This structure helps accommodate inverse vulcanization (IV) reactions and ensures the uniform distribution of the final product (S-DIB). To evaluate the adsorption quantity of pyrene on the carbon surface, standard solutions of varying pyrene concentrations in dimethyl sulfoxide (DMSO) were prepared and analyzed using Ultraviolet–visible spectroscopy (UV-VIS). A linear relationship is fitted between the intensity of these peaks with the standard pyrene solution. Therefore, the concentration in the filtrate is verified to be approximately 2 mM, in contrast to the initial concentration of 10 mM before adsorption. This observed concentration decrease implies an effective adsorption of pyrene molecules onto the HPC surface. To further investigate the catalytic effect of Cl-pyrene and NH2-pyrene for sulfur redox reactions, potentiostatic nucleation of Li2S on the HPC, Cl-HPC and NH2-HPC electrodes were conducted to clarify the involved multiphase transition process. As shown in Figure 3, the capacity of precipitated Li2S on Cl-HPC (160.62 mAh gS −1) and NH2-HPC (135.75 mAh gS −1) are both higher than that on HPC (99. 93 mAh gS −1). As a result, superior to S-DIB/HPC, the S-DIB/Cl-HPC cathode exhibits a higher initial specific capacity of 1208 mA h g−1 at 0.1 C and a capacity of 643 mA h g−1 at 3 C, and still retain 913 mAh g−1 while returning to 0.1 C. Furthermore, the S-DIB/NH2-HPC cathode possesses excellent cyclability with a high capacity retention of 652 mAh g−1 at 1 C over 300 cycles, yielding an average capacity decline of only 0.076% per cycle. Additionally, we investigate the impact of native surface groups on the deposition of lithium sulfide and the conversion of polysulfides. Figure 1

Degradation of pyrene at high concentrations in sediment and the implications for the microbiome in microbial electrochemical systems

The polycyclic aromatic hydrocarbons (PAHs) frequently accumulate in sediments, particularly those near industrial sites. The efficacy of microbial electrochemical systems (MESs) in electricity generation and PAHs degradation is intricately linked to the microbiome’s response to high contaminant levels. Metabolomics and metagenomics were applied to elucidate the impact of a high pyrene concentration on the functional structure and metabolic dynamics of sediment microbiomes within MES. In sediment with a high pyrene concentration, both the electrical output of MES and efficiency of their microbiomes in degrading organic substrates and pyrene were markedly reduced. These conditions were associated with the enrichment of PAH-degrading microorganisms, such as Hydrogenophaga and Flavobacterium. Analyses of metabolites and genetic profiles revealed that metabolic pathways were primarily influenced in MES exposed to low pyrene concentrations whereas fewer metabolic pathways were activated in MES exposed to high concentrations; instead, pathways representing functions critical for microbial survival and communication were activated as well. According to enzymatic analyses, low pyrene levels promoted carbohydrate metabolism by sediment microorganisms, whereas high levels had an inhibitory effect. An examination of electron transport enzymes revealed that intracellular electron transfer was facilitated by both low and high concentrations. However, high levels impeded enzymes associated with outer membrane electron transfer, hindering electron movement from intracellular to extracellular electron acceptors and thus negatively affecting the electrical output of MES. Our study provides crucial theoretical insight and mechanistic understanding for addressing the challenges that may be encountered when MES are used to treat pyrene-contaminated sediment near industrial sites.

A baseline assessment of contamination in the Sacramento deep water ship channel

The Sacramento Deep Water Ship Channel (SDWSC) in the San Francisco Estuary, which is an active commercial port, is critical habitat for pelagic fish species including delta smelt (Hypomesus transpacificus), longfin smelt (Spirinchus thaleichthys), and Sacramento perch (Archoplites interruptus). Pelagic organism decline has been attributed to covarying factors such as manipulation of habitat, introduction of invasive species, decrease in food production, and contaminant exposure. Quantification of bioavailable toxicant loads in the SDWSC is limited despite previous surveys that have detected elevated contaminant concentrations in the sediments. Therefore, the focus of the present study was to characterize the bioavailability of the contaminants in the SDWSC from six sites along the channel. At each site, organochlorine pesticides (OCPs), pyrethroid insecticides, polyaromatic hydrocarbons (PAHs), and polychlorinated biphenyls (PCBs) were quantified in sediment, zooplankton, and suspended solids. In addition, Tenax extraction was used to measure the bioaccessible fraction of sediment-associated contaminants freely dissolved in the water. Bioaccessible contaminants in the sediment provided an uptake route for these stressors into invertebrates and fish with bioaccessible OCPs being found at all sites, particularly 4,4′-dichlorodiphenyldichloroethylene (DDE). Bifenthrin was the only pyrethroid detected in the chosen matrices and it was found at concentrations below levels of concern. Bioaccessible PAHs were found at all sites, with highest detections for phenanthrene and pyrene. No PCBs were detected in sediments, but were detected in both suspended solids and zooplankton. Contaminant concentrations overall were significantly higher in suspended solids, followed by zooplankton and sediments. The highest sediment concentrations of DDE, fluoranthene, pyrene, and dibenzo[a,h]anthracene exceeded sediment quality benchmarks indicating potential risk to sediment-dwelling species. Finally, elevated contaminant levels were found in both suspended solids and zooplankton, suggesting additional risk to pelagic species in the SDWSC.

AQUA-GAPS/MONET-Derived Concentrations and Trends of PAHs and Polycyclic Musks across Global Waters.

Polycyclic aromatic hydrocarbons (PAHs), released from petrogenic, pyrogenic or diagenetic sources (degradation of wood materials), are of global concern due to their adverse effects, and potential for long-range transport. While dissolved PAHs have been frequently reported in the literature, there has been no consistent approach of sampling across water bodies. Passive samplers from the AQUA/GAPS-MONET initiative were deployed at 46 sites (28 marine and 18 freshwater), and analyzed for 28 PAHs and six polycyclic musks (PCMs) centrally. Freely dissolved PAH concentrations were dominated by phenanthrene (mean concentration 1500 pg L-1; median 530 pg L-1) and other low molecular weight compounds. Greatest concentrations of phenanthrene, fluoranthene, and pyrene were typically from the same sites, mostly in Europe and North America. Of the PCMs, only galaxolide (72% of samples) and tonalide (61%) were regularly detected, and were significantly cross-correlated. Benchmarking of PAHs relative to penta- and hexachlorobenzene confirmed that the most remote sites (Arctic, Antarctic, and mountain lakes) displayed below average PAH concentrations. Concentrations of 11 of 28 PAHs, galaxolide and tonalide were positively correlated (P < 0.05) with population density within a radius of 5 km of the sampling site. Characteristic PAH ratios gave conflicting results, likely reflecting multiple PAH sources and postemission changes.

Biodegradation of high molecular weight polycyclic aromatic hydrocarbons by Sarocladium terricola strain PYR-233 isolated from petrochemical contaminated sediment

Polycyclic aromatic hydrocarbons (PAHs) were frequently found in sediment and were primarily treated through microbial degradation. Thus, efficient management of PAH pollution requires exploring the molecular degradation mechanisms of PAHs and expanding the pool of available microbial resources. A fungus (identified as Sarocladium terricola strain RCEF778) with the remarkable ability to degrade pyrene was screened from sediment near a petrochemical plant, and its growth and pyrene degradation characteristics were comprehensively investigated. The results showed that the fungus exhibited great effectiveness in pyrene degradation, with a degradation ratio of 88.97% at 21 days at the conditions: 35 °C, pH 7, 10 mg L−1 initially pyrene concentration, 3% supplementary salt, and glucose supplementation. The generation and concentration variation of the intermediate products were identified, and the results revealed that the fungus degraded pyrene through two pathways: by salicylic acid and by phthalic acid. Three sediments (M1, M2, M3), each exhibiting different levels of PAH pollution, were employed to examine the effectiveness of fungal degradation of PAHs in practical sediment samples. These data showed that with the fungus, the degradation ratios ranged from 13.64% to 23.50% for 2–3 rings PAHs, 40.93%–49.41% for 4 rings PAHs, and 39.59%–48.07% for 5–6 rings PAHs, which were significantly higher than those for the sediment without the fungus and confirmed the excellent performance of the fungal. Moreover, the Gompertz model was employed to analyze the degradation kinetics of 4-rings and 5–6 rings PAHs in these sediments, and the results demonstrated that the addition of the fungus could significantly increase the maximum degradation ratio, degradation start-up rate and maximum degradation rate of 4-rings and 5–6 rings PAHs and shorten the time required to reach the maximum degradation rate. This study not only supplied fungal materials but also established crucial theoretical foundations for the development of bioremediation technologies aimed at high molecular weight PAH-contaminated sediments.

Cohesive phycoremediation of pyrene by freshwater microalgae Selenastrum sp. and biodiesel production and its assessment.

In this study, the freshwater microalgae Selenastrum sp. was assessed for the effective degradation of pyrene and simultaneous production of biodiesel from pyrene-tolerant biomass. The growth of algae was determined based on the cell dry weight, cell density, chlorophyll content, and biomass productivity under different pyrene concentrations. Further, lipids from pyrene tolerant culture were converted into biodiesel by acid-catalyzed transesterification, which was characterized for the total fatty acid profile by gas chromatography. Increased pyrene concentration revealed less biomass yield and productivity after 20days of treatment, indicating potent pyrene biodegradation by Selenastrum sp. Biomass yield was unaffected till the 20mg/L pyrene. A 95% of pyrene bioremediation was observed at 20days of culturing. Lipid accumulation of 22.14%, as evident from the estimation of the total lipid content, indicated a marginal increase in corroborating pyrene stress in the culture. Fatty acid methyl esters yield of 63.06% (% per 100g lipids) was noticed from the pyrene tolerant culture. Moreover, fatty acid profile analysis of biodiesel produced under 10mg/L and 20mg/L pyrene conditionshowed escalated levels of desirable fatty acids in Selenastrum sp., compared to the control. Further, Selenastrum sp. and other freshwater microalgae are catalogued for sustainable development goals attainment by 2030, as per the UNSDG (United Nations Sustainable Development Goals) agenda. Critical applications for the Selenastrum sp. in bioremediation of pyrene, along with biodiesel production, are enumerated for sustainableand renewable energy production and resource management.

Comparison of chemical contaminant measurements using CLAM, POCIS, and silicone band samplers in estuarine mesocosms.

Discrete water samples represent a snapshot of conditions at a particular moment in time and may not represent a true chemical exposure caused by changes in chemical input, tide, flow, and precipitation. Sampling technologies have been engineered to better estimate time-weighted concentrations. In this study, we consider the utility of three integrative sampling platforms: polar organic chemical integrative sampler (POCIS), silicone bands (SBs), and continuous, low-level aquatic monitoring (CLAM). This experiment used simulated southeastern salt marsh mesocosm systems to evaluate the response of passive (POCIS, SBs) and active sampling (CLAM) devices along with discrete sampling methodologies. Three systems were assigned to each passive sampler technology. Initially, all tanks were dosed at nominal (low) bifenthrin, pyrene, and triclosan concentrations of 0.02, 2.2, and 100 µg/L, respectively. After 28 days, the same treatment systems were dosed a second time (high) with bifenthrin, pyrene, and triclosan at 0.08, 8.8, and 200 µg/L, respectively. For passive samplers, estimated water concentrations were calculated using published or laboratory-derived sampling rate constants. Chemical residues measured from SBs resulted in high/low ratios of approximately 2x, approximately 3x, and 1x for bifenthrin, pyrene, and triclosan. A similar pattern was calculated using data from POCIS samples (~4x, ~3x, ~1x). Results from this study will help users of CLAM, POCIS, and SB data to better evaluate water concentrations from sampling events that are integrated across time. Integr Environ Assess Manag 2024;20:1384-1395. © 2024 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC).

Effect of ammonia environment on the quality of boxed non-dairy cream

Ammonia leakage in food cold storage have adverse impact on the quality of food, which may be related to ammonia concentration and exposure time, but there is a lack of data support. In this paper, the quality of boxed non-dairy cream exposed to ammonia environment (0 (CK), 100, 500, and 1000 mL m−³) at −18 °C for 6 day were evaluated. Results showed that no ammonia residue was detected in the boxed non-dairy cream exposed for 6 days. There were no significant differences (P > 0.05) in the color value, odor, pH value, and sensory score of the non-dairy cream under the four ammonia groups during the same exposure time. And peroxide values was far below the standards limit, and benzo (α) pyrene content of all the cream groups were not detected The results indicated that all the boxed non-dairy cream in this experiment had no quality deterioration and food safety risk.

Numerical study on kinetics of tar production and mechanism of benzene formation during corn straw gasification

Tar production is a key factor hindering the industrialization of biomass gasification technology. Understanding the mechanisms of tar formation can help predict and reduce tar yield. A gasification model was proposed to investigate the effects of oxygen ratio (OR) and temperature on products formation. Its accuracy was validated using experimental data. The relative content of PAHs from corn straw gasification decreased from 95 % to 53 % with OR and temperature increasing, indicating PAHs relative content could be decreased by increasing OR and temperature. The concentrations of phenanthrene from cellulose and corn straw gasification at 900 °C were 0.85 and 378 ppm, separately. The concentrations of pyrene were 52 and 558 ppm, respectively. The content of PAHs from cellulose gasification was much less than that from corn straw gasification. However, the contribution of cellulose to PAHs formation increased with temperature increasing. Furthermore, the mechanism of benzene formation was analyzed qualitatively and quantitatively. C2H2, C3H3, and C4H6 were main precursors and exhibited a considerable role in benzene formation. H, OH, CH3, and C6H5 were the key radicals. The analysis results indicated that CH3→C2H2→C3H3→benzene and C2H3/C2H4→C4H6→n-C4H5→benzene were two main paths for benzene formation during corn straw gasification.

Identification of potential markers, key aroma compounds, and hazardous compounds in different types of smoked meat products

SummaryThis study aimed to characterise the volatile aroma and hazardous compounds presented in smoked meat from various regions and types. The analysis was conducted using chromatographic/mass spectrometric techniques. In six types of smoked meat, 15 of the 40 key aroma compounds were found to be co‐occurring. The highest contributor among them was 2‐methoxy‐phenol. Compared to other smoked meat, Norharman was more abundant in smoked pork with a range of 4.97~81.04 ng g−1, and Nε‐carboxymethyl lysine (CML) and Nε‐carboxyethyl lysine (CEL) were higher in smoked pork and chicken with a range of 9.32~138.91 μg g−1 and 6.35~141.74 μg g−1, respectively. Benzo[a]pyrene (BaP) content did not exceed 5 μg kg−1 in any of the samples. Concerning aroma compounds, phenolics were higher in smoked pork and mutton, aldehydes in smoked duck and goose and nitrogenous compounds mainly in smoked chicken. Additionally, 12 key potential markers were identified for distinguishing between different regions and types of smoked meat. In comparison, southwest smoked meat showed higher levels of key phenolics such as 2‐methoxy‐phenol. This result contributed to a comprehensive understanding of smoked meat while being valuable in both retaining key aroma and reducing hazardous compounds in later stages of new product development.

Adsorption of Pyrene and Arsenite by Micro/Nano Carbon Black and Iron Oxide.

Polycyclic aromatic hydrocarbons (PAHs) and arsenic (As) are common pollutants co-existing in the environment, causing potential hazards to the ecosystem and human health. How their behaviors are affected by micro/nano particles in the environment are still not very clear. Through a series of static adsorption experiments, this study investigated the adsorption of pyrene and arsenite (As (III)) using micro/nano carbon black and iron oxide under different conditions. The objectives were to determine the kinetics and isotherms of the adsorption of pyrene and As (III) using micro/nano carbon black and iron oxide and evaluate the impact of co-existing conditions on the adsorption. The microstructure of micro/nano carbon black (C 94.03%) is spherical-like, with a diameter of 100-200 nm. The micro/nano iron oxide (hematite) has irregular rod-shaped structures, mostly about 1 µm long and 100-200 nm wide. The results show that the micro/nano black carbon easily adsorbed the pyrene, with a pseudo-second-order rate constant of 0.016 mg/(g·h) and an adsorption capacity of 283.23 μg/g at 24 h. The micro/nano iron oxide easily adsorbed As (III), with a pseudo-second-order rate constant of 0.814 mg/(g·h) and an adsorption capacity of 3.45 mg/g at 24 h. The mechanisms of adsorption were mainly chemical reactions. Micro/nano carbon black hardly adsorbed As (III), but its adsorption capability for pyrene was reduced by the presence of As (III), and this effect increased with an increase in the As (III) concentration. The adsorbed pyrene on the micro/nano black carbon could hardly be desorbed. On the other hand, the micro/nano iron oxide could hardly adsorb the pyrene, but its adsorption capability for As (III) was increased by the presence of pyrene, and this effect increased with an increase in the pyrene concentration. The results of this study provide guidance for the risk management and remediation of the environment when there is combined pollution of PAHs and As.

Viscosities and Densities of Binary and Ternary Mixtures of Aliphatic and Polyaromatic Hydrocarbons: Pyrene +1-Methylnaphthalene + Dodecane at T = (293.15 to 343.15) K. Experiment and Modeling.

This work presents new experimental viscosity and density data for aromatic and polyaromatic compounds in binary and ternary pyrene, 1-methylnaphthalene, and dodecane mixtures. The lack of experimental viscosity data for these mixtures requires the development of a new database, which is vital for understanding the behavior of mixtures in more complex systems, such as asphaltenes and fuels. The mixtures proposed in this work have been measured over a temperature range of (293.15 to 343.15) K at atmospheric pressure. Several mixture compositions have been studied at these conditions: 1.0, 2.5, 5.0, 7.5, 10.0, 12.5, and 15.0% pyrene mass fraction. The concentration of pyrene correlates with an increase in the viscosity and density values. At the lowest temperature in binary mixtures, the corresponding values reach 4.4217 mPa·s for viscosity and 1.0447 × 103 kg·m-3 for density, respectively. In ternary mixtures, the introduction of dodecane leads to the lowest maximum values of 3.5555 mPa·s for viscosity and 1.0112 × 103 kg·m-3 for density at the same temperature. The experimental data have been employed for the specific modification of viscosity models. These modifications could facilitate the prediction of the viscosity of mixtures that are more complex than those presented in this work. Various viscosity models have been employed, such as Linear, Ratcliff and Khan, modified UNIFAC-Visco, and Krieger-Dougherty. The settings in the models used reliably reproduce the experiment reliably. However, the Ratcliff model agrees excellently with the experiment, having a low standard deviation (2.0%) compared to other models. Furthermore, a model based on the equation of state of Guo is proposed to predict the viscosity values by modifying the specific parameters and adjusting them to the mixtures proposed in this work. The results from this study are compared to previous work, where pyrene, toluene, and heptane mixtures were analyzed. In this case, we find that the decrease of aggregation grade in the present systems is predicted by the model fixed in this work.

Air Pollution and Primary DNA Damage among Zagreb (Croatia) Residents: A Cross-Sectional Study.

More than eight million premature deaths annually can be attributed to air pollution, with 99% of the world's population residing in areas below recommended air quality standards. Hence, the present study aimed to examine the association between primary DNA damage and air pollution data among 123 participants enrolled between 2011 and 2015 in Zagreb, Croatia. While most measured air pollutants adhered to regulatory limits, benzo[a]pyrene concentrations bound to PM10 exceeded them. Factorial analysis narrowed down air pollution data to four exposure factors (particulate matter, two metal factors, and other pollutants). Despite the absence of significant positive associations between modeled air pollution exposure factors and comet assay descriptors (tail length, tail intensity, tail moment, and highly damaged nuclei), the critical health implications of air pollution warrant further investigations, particularly with biomarkers of exposure and different biomarkers of effect in populations facing air pollution exposure.