Quenching residual H2O2 from UV/H2O2 with granular activated carbon: A significant impact of bicarbonate.

UV/H2O2 has been used as an advanced oxidation process to remove organic micropollutants from drinking water. It is essential to quench residual H2O2 to prevent increased chlorine demand during chlorination/chloramination and within distribution systems. Granular activated carbon (GAC) filter can quench the residual oxidant and eliminate some of the dissolved organic matter. However, knowledge on the kinetics and governing factors of GAC quenching of residual H2O2 from UV/H2O2 and the mechanism underlying the enhancement of the process by HCO3- is limited. Therefore, this study aimed to analyse the kinetics and influential factors, particularly the significant impact of bicarbonate (HCO3-). H2O2 decomposition by GAC followed first-order kinetics, and the rate constants normalised by the GAC dosage (kn) were steady (1.6 × 10-3 L g-1 min-1) with variations in the GAC dosage and initial H2O2 concentration. Alkaline conditions favour H2O2 quenching. The content of basic groups exhibited a stronger correlation with the efficiency of GAC in quenching H2O2 than did the acidic groups， with their specific kn values being 8.9 and 2.4 min-1 M-1, respectively. The presence of chloride, sulfate, nitrate, and dissolved organic matter inhibited H2O2 quenching, while HCO3- promoted it. The interfacial hydroxyl radical (HO•) zones were visualised on the GAC surface, and HCO3- addition increased the HO• concentration. HCO3- increased the concentration of persistent free radicals (PFRs) on the GAC surface, which mainly contributed to HO• generation. A significant enhancement of HCO3- on H2O2 quenching by GAC was also verified in real water. This study revealed the synergistic mechanism of HCO3- and GAC on H2O2 quenching and presents the potential applications of residual H2O2 in the H2O2-based oxidation processes.

Estimated health effects from domestic use of gaseous fuels for cooking and heating in high-income, middle-income, and low-income countries: a systematic review and meta-analyses.

BACKGROUND: Exposure to household air pollution from polluting domestic fuel (solid fuel and kerosene) represents a substantial global public health burden and there is an urgent need for rapid transition to clean domestic fuels. Gas for cooking and heating might possibly affect child asthma, wheezing, and respiratory health. The aim of this review was to synthesise the evidence on the health effects of gaseous fuels to inform policies for scalable clean household energy. METHODS: In this systematic review and meta-analysis, we summarised the health effects from cooking or heating with gas compared with polluting fuels (eg, wood or charcoal) and clean energy (eg, electricity and solar energy). We searched PubMed, Scopus, Web of Science, MEDLINE, Cochrane Library (CENTRAL), Environment Complete, GreenFile, Google Scholar, Wanfang DATA, and CNKI for articles published between Dec 16, 2020, and Feb 6, 2021. Studies eligible for inclusion had to compare gas for cooking or heating with polluting fuels (eg, wood or charcoal) or clean energy (eg, electricity or solar energy) and present data for health outcomes in general populations. Studies that reported health outcomes that were exacerbations of existing underlying conditions were excluded. Several of our reviewers were involved in screening studies, data extraction, and quality assessment (including risk of bias) of included studies; 20% of studies were independently screened, extracted and quality assessed by another reviewer. Disagreements were reconciled through discussion with the wider review team. Included studies were appraised for quality using the Liverpool Quality Assessment Tools. Key health outcomes were grouped for meta-analysis and analysed using Cochrane's RevMan software. Primary outcomes were health effects (eg, acute lower respiratory infections) and secondary outcomes were health symptoms (eg, respiratory symptoms such as wheeze, cough, or breathlessness). This study is registered with PROSPERO, CRD42021227092. FINDINGS: 116 studies were included in the meta-analysis (two [2%] randomised controlled trials, 13 [11%] case-control studies, 23 [20%] cohort studies, and 78 [67%] cross-sectional studies), contributing 215 effect estimates for five grouped health outcomes. Compared with polluting fuels, use of gas significantly lowered the risk of pneumonia (OR 0·54, 95% CI 0·38-0·77; p=0·00080), wheeze (OR 0·42, 0·30-0·59; p<0·0001), cough (OR 0·44, 0·32-0·62; p<0·0001), breathlessness (OR 0·40, 0·21-0·76; p=0·0052), chronic obstructive pulmonary disease (OR 0·37, 0·23-0·60; p<0·0001), bronchitis (OR 0·60, 0·43-0·82; p=0·0015), pulmonary function deficit (OR 0·27, 0·17-0·44; p<0·0001), severe respiratory illness or death (OR 0·27, 0·11-0·63; p=0·0024), preterm birth (OR 0·66, 0·45-0·97; p=0·033), and low birth weight (OR 0·70, 0·53-0·93; p=0·015). Non-statistically significant effects were observed for asthma in children (OR 1·04, 0·70-1·55; p=0·84), asthma in adults (OR 0·65, 0·43-1·00; p=0·052), and small for gestational age (OR 1·04, 0·89-1·21; p=0·62). Compared with electricity, use of gas significantly increased risk of pneumonia (OR 1·26, 1·03-1·53; p=0·025) and chronic obstructive pulmonary disease (OR 1·15, 1·06-1·25; p=0·0011), although smaller non-significant effects were observed for higher-quality studies. In addition, a small increased risk of asthma in children was not significant (OR 1·09, 0·99-1·19; p=0·071) and no significant associations were found for adult asthma, wheeze, cough, and breathlessness (p>0·05). A significant decreased risk of bronchitis was observed (OR 0·87, 0·81-0·93; p<0·0001). INTERPRETATION: Switching from polluting fuels to gaseous household fuels could lower health risk and associated morbidity and mortality in resource-poor countries where reliance on polluting fuels is greatest. Although gas fuel use was associated with a slightly higher risk for some health outcomes compared with electricity, gas is an important transitional option for health in countries where access to reliable electricity supply for cooking or heating is not feasible in the near term. FUNDING: WHO.

Magnetic activated carbon from spent coffee grounds: iron-catalyzed CO2 activation mechanism and adsorption of antibiotic lomefloxacin from aqueous medium.

The facile fabrication of low-cost adsorbents possessing high removal efficiency and convenient separation property is an urgent need for water treatment. Herein, magnetic activated carbon was synthesized from spent coffee grounds (SCG) by Fe-catalyzed CO2 activation at 800 °C for 90 min, and magnetization and pore formation were simultaneously achieved during heat treatment. The sample was characterized by N2 adsorption-desorption, XRD, VSM, SEM, and FTIR. Batch adsorption experiments were conducted using lomefloxacin (LMO) as the probing pollutant. Preparation mechanism was revealed by TG-FTIR and XRD. Experimental results showed that Fe3O4 derived from Fe species can be reduced to Fe by carbon at high temperatures, followed by subsequent reoxidation to Fe3O4 by CO2, and the redox cycle between Fe and Fe3O4 favored the formation of pores. The promotion effects of Fe species on CO2 activation can be quantitatively reflected by the yield of CO as the signature gaseous product, and the suitable activation temperate range was determined to be 675 to 985 °C. The BET surface area, total pore volume, and saturated magnetization value of the product were 586 m2 g-1, 0.327 cm3 g-1, and 11.59 emu g-1, respectively. The Langmuir model was applicable for the adsorption isotherm data for LMO with the maximum adsorption capacity of 95 mg g-1, and thermodynamic analysis revealed that the adsorption process was endothermic and spontaneous. This study demonstrated that Fe-catalyzed CO2 activation was an effective method of converting SCG into magnetic separable adsorbent for LMO removal from aqueous medium.

Accurate low-dose exposure assessment of benzene and monoaromatic compounds by diffusive sampling: sampling and analytical method validation according to ISO 23320 for radiello® samplers packed with activated charcoal.

The research study aimed at providing an accurate low-dose benzene exposure assessment method, by validating diffusive monitoring techniques for benzene personal exposure measurements at workplaces where benzene concentrations are expected in the low ppb range, such as in the present-day chemical, petrochemical, foundry, and pharmaceutical industry. The project was aimed at addressing the need for a robust and fully validated method to perform personal exposure measurements considering that the occupational exposure limit value for benzene is going to be significantly lowered in the next few years. Diffusive sampling offers a reliable alternative to pumped sampling methods, intrinsic safety in potentially explosive atmospheres, lightness, and ease of use. In this study, the radiello® diffusive sampler, with the packed activated charcoal RAD130 adsorbing substrate [suitable for solvent desorption and analysis by high-resolution gas chromatography-flame ionization detection (HRGC-FID)], was used. The experiments have been conducted following the ISO 23320 standard in the range from 0.005 to 0.1 ppm (16 to 320 µg/m3), yielding a full validation of the sampling and analytical method. The sampler performances have fulfilled all requisites of the ISO 23320 standard, in particular: bias due to the selection of a non-ideal sorbent is lower than 10% (no significant back diffusion of benzene due to concentration change in the atmosphere); bias due to storage of samples for up to 2 months is lower than 10%; nominal uptake rate for benzene on RAD130 is 74.65 mL/min; and expanded uncertainty of the sampling and analytical method is 20.6%. The sampling and analytical method is therefore fit-for-purpose for the personal exposure measurements aimed at testing compliance with occupational exposure limit values for benzene. The method is also fit for short-duration exposure monitoring related to specific tasks, and other volatile organic compounds, usually found in the same workplaces, such as aliphatic and aromatic hydrocarbons and some oxygenated compounds, have also been studied. In particular, n-hexane and isopropyl benzene, whose classification is currently under revision, can be efficiently monitored by this technique.

Short-term impact of different doses of spent coffee grounds, salt, and sand on soil chemical and hydrological properties in an urban soil.

Natural and human activities have deteriorated urban soil's health and ecological functions as compared to forest soils. Therefore, we hypothesized that any intervention in poor quality soil in urban area will change their chemical and water retention properties. The experiment was conducted in Krakow (Poland) in completely randomized design (CRD). The soil amendments used in this experiment consisted of control, spent coffee grounds (SCGs), salt, and sand (1 and 2 t ha-1) in order to evaluate the impact of these soil amendments on the urban soil chemical and hydrological properties. Soil samples were collected after 3 months of soil application. The soil pH, soil acidity (me/100 g), electrical conductivity (mS/cm), total carbon (%), CO2 emission (g m-2 day-1), and total nitrogen (%) were measured in laboratory condition. The soil hydrological properties like volumetric water content (VWC), water drop penetration time (WDPT), current water storage capacity (Sa), water storage capacity after 4 and 24 h (S4 and S24), and capillary water Pk (mm) were also determined. We noted variations in soil chemical and water retention properties in urban soil after the application of SCGs, sand, and salt. It was observed that SCGs (2 t ha-1) has reduced soil pH and nitrogen (%) by 14 and 9%, while the incorporation of salt resulted in maximum soil EC, total acidity, and soil pH. The soil carbon (%) and CO2 emission (g m-2 day-1) were enhanced and declined by SCGs amendment. Furthermore, the soil hydrological properties were significantly influenced by the soil amendment (spent coffee grounds, salt, and sand) application. Our results showed that spent coffee grounds mixing in urban soil has considerably enhanced the soil VWC, Sa, S4, S24, and Pk, whereas it decreased the water drop penetration time. The analysis showed that the single dose of soil amendments had not improved soil chemical properties very well. Therefore, it is suggested that SCGs should be applied more than single dose. This is a good direction to look for ways to improve the retention properties of urban soil and you can consider combining SCGs with other organic materials like compost, farmyard manure, or biochar.

Anthracological study of a Chalcolithic funerary deposit from Perdigões (Alentejo, Portugal): A new analytical methodology to establish the wood burning temperature.

Anthracological analyses of charcoal samples retrieved from Pit 16 of Perdigões (Reguengos de Monsaraz, Portugal), a secondary deposition of cremated human remains dated back to the middle of the 3rd millennium BC, enabled the identification of 7 different taxa: Olea europaea, Quercus spp. (evergreen), Pinus pinaster, Fraxinus cf. angustifolia, Arbutus unedo, Cistus sp. and Fabaceae. All taxa are characteristic of both deciduous and evergreen Mediterranean vegetation, and this data might indicate that the gathering of woods employed for the human cremation/s occurred either on site, or in its vicinity. However, considering both the large distribution of the identified taxa and data about human mobility, it is not possible to conclusively determine the origin of the wood used in the cremation(s). Chemometric analysis were carried out to estimate the absolute burning temperature of woods employed for the human cremation/s. An in-lab charcoal reference collection was created by burning sound wood samples of the three main taxa identified from Pit 16, Olea europaea var. sylvestris, Quercus suber (evergreen type) and Pinus pinaster, at temperatures between 350 and 600 °C. The archaeological charcoal samples and the charcoal reference collection were chemically characterized by using mid-infrared (MIR) spectroscopy in the 1800-400 cm-1 range, and Partial Least Squares (PLS) regression method was used to build calibration models to predict the absolute combustion temperature of the archaeological woods. Results showed successful PLS forecasting of burn temperature for each taxon (significant (P <0.05) cross validation coefficients). The anthracological and chemometric analysis evidenced differences between the taxa coming from the two stratigraphic units within the Pit, SUs 72 and 74, suggesting that they may come from two different pyres or two different depositional moments.

Effects of organic carbon/elemental carbon and particle size on inhalation bioaccessibility of particle-bound PAHs.

Bioaccessible fractions of particle-bound hydrophobic organic compounds (HOCs) are critical to evaluating human inhalation exposure risk. However, the key factors for controlling the release of HOCs into the lung fluid are not adequately examined. To address this issue, eight particle size fractions (0.056-18 µm) from different particle emission sources (barbecue and smoking) were collected and incubated with an in vitro method for determining inhalation bioaccessibilities of polycyclic aromatic hydrocarbons (PAHs). The bioaccessible fractions of particle-bound PAHs were 35-65% for smoke-type charcoal, 24-62% for smokeless-type charcoal, and 44-96% for cigarette. The size distributions of bioaccessible fractions of 3-4 ring PAHs were symmetric with the patterns of their masses, characterized as a unimodal distribution with both the trough and peak at 0.56-1.0 µm. Analysis from machine learning showed that chemical hydrophobicity appeared to be the most significant factor affecting inhalation bioaccessibility of PAHs, followed by organic carbon and elemental carbon contents. Particle size seemed to have little effect on the bioaccessibility of PAHs. A compositional analysis of human inhalation exposure risk from total concentration, deposition concentration, and bioaccessible deposition concentration in alveolar region showed a shift in the key particle size from 0.56-1.0 µm to 1.0-1.8 µm and an increasing in the contributions of 2-3 ring PAHs to risk for cigarette due to the high bioaccessible fractions. These results suggested the significance of particle deposition efficiency and bioaccessible fractions of HOCs in risk assessment.

[Distribution, Tansformation, and Fate of Per-and Polyfluoroalkyl Substances in Drinking Water Treatment].

Per-and polyfluoroalkyl substances (PFASs) are present in surface water, tap water, and even commercial drinking water and pose a threat to human health. In this study, the occurrence and transformation of 14 PFASs were studied in large drinking water treatment plants (DWTPs) with Taihu Lake as the source, and the results showed that a total of 10 PFASs were detected in the water samples, indicating that PFAS were widely distributed in drinking water. The total concentration of PFASs in raw water was 127.4 ng·L-1, with the highest concentration being that of pentadecafluorooctanoic acid (PFOA, 49.8 ng·L-1). Pre-ozone caused a reverse increase in the concentration of PFASs, which may have been due to the presence of precursors or conversion from short to long chains. PFASs were not effectively removed by conventional treatment processes, andozone-biological activated carbon (O3-BAC) had a dominant role in the removal of PFASs (20.74%) from DWTPs. O3-BAC, the main removal process for DWTPs, contained high concentrations of PFASs in the backwash water with similar distribution characteristics to the raw water. Using a pilot plant, five common filter backwash water treatment processes were compared, and the results showed that GAC-ultrafiltration could adsorb and retain a certain amount of PFASs while ensuring a high removal rate of turbidity (99.08%). The 3D-EEM analysis indicated that GAC-ultrafiltration could also remove most of the fluorescent micro-pollutants, and for raw water containing high concentrations of PFASs DWTPs, it is practical to use it as a filter backwash water reuse treatment process.

Contamination and removal efficiency of microplastics and synthetic fibres in a conventional drinking water treatment plant in Geneva, Switzerland.

Although it is known that freshwater resources are contaminated with microplastics (MPs), still limited information is known about the efficiency of large drinking water treatment plants (DWTP) to remove microplastics. Moreover, reported concentrations of MPs in drinking water variates from some units to thousands of units per litre and the sampling volumes used for MPs analysis are generally heterogeneous and limited. The present study evaluates the removal of MPs and synthetic fibres in the main DWTP of Geneva, Switzerland, by considering large sampling volumes at different time intervals. Furthermore, contrary to other studies, this DWTP does not count with a clarification process before sand filtration and coagulated water is sent directly to sand filtration. In this study a distinction is made between microplastics as fragments, films, pellets, and synthetic fibres. Raw water and effluents of each filtering mass (sand and activated carbon filtration) are analysed for the presence of MPs and synthetic fibres with sizes ≥63 µm using infrared spectroscopy. Concentrations of MPs in raw water range from 25.7 to 55.6 MPs/m3 and in treated water from 0 to 4 MPs/m3, respectively. Results show that 70 % of MPs are retained during sand filtration and total removal is equal to 97 % in treated water after activated carbon filtration. Concentration of identified synthetic fibres is low (average value of 2 synthetic fibres/m3) and constant in all steps of water treatment. Chemical composition of microplastics and synthetic fibres is found more heterogeneous in raw water than after sand filtration and activated carbon filtration, indicating the persistence of some types of plastics (like polyethylene and polyethylene terephthalate) in water treatment processes. Heterogeneities in MP concentrations are observed from one sampling campaign to another, indicating significant variations of MP concentrations in raw water.

Indirect Methods to Determine the Risk of Damage to the Health of Firefighters and Children Due to Exposure to Smoke Emission from Burning Wood/Coal in a Controlled Environment.

People are constantly exposed to particulate matter and chemicals released during fires. However, there are still few studies on gas and particulate emissions related to exposure to burning firewood and charcoal during forest fires, making it difficult to understand the effects on the health of the population. The objective of this study was to quantify the metal(loid)s present in the smoke from wood and charcoal fires through the deposition of metals in beef topside and pork loin, considering the routes of skin exposure, inhalation, and ingestion, contributing to the understanding of metals in the increase of the risks of cancer and mortality associated with firefighting and children. The concentrations of metals [aluminum (Al), chromium (Cr), copper (Cu), iron (Fe), magnesium (Mg), manganese (Mn), molybdenum (Mo), vanadium (V), zinc (Zn)] and metalloids arsenic (As) were determined by inductively coupled plasma-mass spectrometry (ICP OES) after microwave digestion. Moreover, we assessed the associated risk regarding the elemental intake of these elements through the smoke, using the hazard quotient (HQ), hazard index (HI), Total Hazard Index (HIt), and carcinogenic risk (CR). All samples had results for HQ and HIt < 1, indicating a non-potential health risk. However, the carcinogenic risks posed by As and Cr via the three exposure pathways (except for inhalation exposure to children and adults, and by Cr via ingestion and inhalation for children and adults) exceeded the standard threshold. In conclusion, continuous exposure of firefighters or children to smoke from fires containing high concentrations of heavy metals such as As and Cr can be harmful to health. The study used animal tissues; thus, new methods must be developed to quantify the concentration of heavy metals deposited in human tissue when humans are exposed to smoke from fires.

Particle and gas phase sampling of PCDD/Fs and dl-PCBs by activated carbon fiber and GC/MS analysis.

Polychlorodibenzo-p-dioxins (PCDDs), polychlorodibenzofurans (PCDFs), and polychlorobiphenyls (PCBs) are semi-volatile compounds and can be partitioned in the atmosphere between the gas and particulate phase, due to their physicochemical properties. For this reason, the reference standard methods for air sampling include a quartz fiber filter (QFF) for the particulate and a polyurethane foam (PUF) cartridge for the vapor phase, and it is the classical and most popular sampling method in the air. Despite the presence of the two adsorbing media, this method cannot be used for the study of the gas-particulate distribution, but only for a total quantification. This study presents the results and the performance aim to validate an activated carbon fiber (ACF) filter for the sampling of PCDD/Fs and dioxin-like PCBs (dl-PCBs) using laboratory and field tests. The specificity, precision, and accuracy of the ACF in relation to the QFF + PUF were evaluated through the isotopic dilution technique, the recovery rates, and the standard deviations. Then the ACF performance was assessed on real samples, in a naturally contaminated area, through parallel sampling with the reference method (QFF + PUF). The QA/QC was defined according to the standard methods ISO 16000-13 and -14 and EPA TO4A and 9A. Data confirmed that ACF meets the requirements for the quantification of native POPs compounds in atmospheric and indoor samples. In addition, ACF provided accuracy and precision comparable to those offered by standard reference methods using QFF + PUF, but with significant savings in terms of time and costs.

Biochar mitigates allelopathic effects in temperate trees.

Many invasive and some native tree species in North America exhibit strong allelopathic effects that may contribute to their local dominance. Pyrogenic carbon (PyC; including soot, charcoal, and black carbon) is produced by the incomplete combustion of organic matter and is widespread in forest soils. Many forms of PyC have sorptive properties that can reduce the bioavailability of allelochemicals. We investigated the potential for PyC produced by controlled pyrolysis of biomass ("biochar" [BC]) to reduce the allelopathic effects of black walnut (Juglans nigra) and Norway maple (Acer platanoides), a common native tree species and a widespread invasive species in North America, respectively. Seedling growth of two native tree species (Acer saccharinum [silver maple] and Betula papyrifera [paper birch]) in response to leaf-litter-incubated soils was examined; litter incubation treatments included leaves of black walnut, Norway maple, and a nonallelopathic species (Tilia americana [American basswood]) in a factorial design with varying dosages; responses to the known primary allelochemical of black walnut (juglone) were also examined. Juglone and leaf litter of both allelopathic species strongly suppressed seedling growth. BC treatments substantially mitigated these effects, consistent with the sorption of allelochemicals; in contrast no positive effects of BC were observed in leaf litter treatments involving controls or additions of nonallelopathic leaf litter. Treatments of leaf litter and juglone with BC increased the total biomass of silver maple by ~35% and in some cases more than doubled the biomass of paper birch. We conclude that BCs have the capacity to largely counteract allelopathic effects in temperate forest systems, suggesting the effects of natural PyC in determining forest community structure, and also the applied use of BC as a soil amendment to mitigate allelopathic effects of invasive tree species.

Biochar Blended with Nitrogen Fertilizer Promotes Maize Yield by Altering Soil Enzyme Activities and Organic Carbon Content in Black Soil.

Biochar and nitrogen fertilizers are known to increase soil carbon storage and reduce soil nitrogen loss as amendments, suggesting a promising strategy for highly effectively increasing soil productivity. However, few studies have explored the mechanisms of their effects on crop yield in terms of active carbon fraction and enzyme activity, which ultimately limits the potential for the application of biochar in combination with nitrogen fertilizers. To evaluate the effect of biochar and nitrogen fertilizer on the improvement of black soils in northeast China, a field experiment was conducted in the black soil to compare and analyze the application methods on total organic carbon (TOC), total nitrogen (TN), enzyme activities, and maize yields. Biochar rates: CK, C1, C2, and C3 (0, 9.8, 19.6, and 29.4 Mg·ha-1); N fertilizer rates: N1/2 and N (30 and 60 kg·ha-1). Results indicated that biochar and N fertilizer amendments significantly ameliorated soil fertility, such as TOC and TN, compared to the unamended soil. The TOC levels in the C3 treatment increased by 35.18% and the TN levels by 23.95%. The improvement in TN is more significant when biochar is blended with N fertilizer. Biochar blended with N fertilizer increased maize cellulase, urease, and invertase activities by an average of 53.12%, 58.13%, and 16.54%, respectively. Redundancy analysis showed that TOC, TN, and MBN contributed 42%, 16.2%, and 22.2%, respectively, to the maize yield indicator. Principal component analysis showed that reduced N fertilizer was more effective in improving yields, with a maximum yield increase of 50.74%. Biochar blended with N fertilizer is an effective strategy to improve the fertility and productivity of black soils in northeast China, while nitrogen fertilizer reduction is feasible and necessary for maintaining grain yield.

Using circular economy principles in the optimisation of sludge-based activated carbon production for the removal of perfluoroalkyl substances.

Massive sewage sludge (SS) production from municipal wastewater treatment plants and the presence of numerous pollutant types render the process of SS treatment and disposal costly and complex. Here, resource recovery from SS was maximised via the optimisation of sludge-based activated carbon (SBAC) production for the removal of poly- and perfluoroalkyl substances (PFASs), while considering economic factors and minimising environmental impacts. SBAC production optimisation was realised under different operating conditions (different ZnCl2 impregnation ratios and different pyrolysis activation temperatures and durations). The sorption capacity of the optimised SBAC with respect to the removal of nine commonly detected PFASs, with environmentally relevant concentrations (∽50 µg/L), from simulated wastewater was evaluated. Economic analysis and life-cycle assessment (LCA) were also performed to determine the feasibility of the process and its potential role in the circular economy. Batch adsorption tests confirmed the high efficiency of the optimised SBACs for PFAS removal (93-100 %), highlighting the possibility of converting SS to SBAC. Economically speaking, the optimised SBAC at 1.5 M ZnCl2, 500 °C, and 0.75 h reduced total production cost by 49 %. Further, the cost could be reduced to as little as 1087 US $/metric-ton compared with that corresponding to the original conditions (2.5 M ZnCl2, 500 °C, 2 h; 2144 US $/metric-ton). LCA results also showed that freshwater ecotoxicity, marine ecotoxicity, and human non-carcinogenic toxicity were the most affected environmental impact indicators, showing a 49 % decrease when ZnCl2 impregnation ratio was reduced from 2.5 to 1.5 M. These findings highlighted the optimal conditions for the production of SBAC with high sorption capacity at a reduced cost and with reduced environmental impacts. Thus, they can serve as valuable tools for decision making regarding the selection of the most sustainable and economically feasible process for PFAS removal.

Activating soil nitrification by co-application of peanut straw biochar and organic fertilizer in a rare earth mining soil.

The intensive mining activities to extract rare earth elements from ion-adsorption rare earth deposits have introduced massive amounts of ammonium into the tailing soils in southern China. Compared to the ubiquitous soil nitrification in cropland, forest, and grassland soils, however, there is no feasible strategy to alleviate the ammonium contamination in tailing soil. Herein, the feasibility to remove ammonium by adding ammonium adsorbents (e.g., biochar, activated carbon, and zeolite), alkaline materials, and organic fertilizer to the rare earth mining soil was explored. The amendment of rice straw biochar, activated carbon, or zeolite in combination with CaCO3 and organic fertilizer showed no significant effect on ammonium removal due to their limited capacity to elevate soil pH. However, the co-application of peanut straw biochar (PSBC), CaCO3, and organic fertilizer activated both the ammonia volatilization and soil nitrification processes. Specifically, the three components functioned as follows: organic fertilizer supplied active ammonia-oxidizing bacteria (AOB); PSBC stimulated AOB proliferation by elevating soil pH above 7.75; CaCO3 ameliorated soil acidity and reduced the lag time for activating soil nitrification. The soil ammonium removal and nitrate accumulation rates were positively correlated to the acid neutralization capacity of PSBC prepared at 400 °C-800 °C. The qPCR and microbial community analysis results indicated that Nitrosomonas europaea was the dominant AOB that was responsible for enhanced soil nitrification. Our findings pave the way for developing cost-effective strategies to remediate ammonium contamination in rare earth mining soils.

Health benefits from substituting raw biomass fuels for charcoal and briquette fuels: In vitro toxicity analysis.

PM2.5 (particulate matters with diameter ≤ 2.5 µm) from biomass fuel combustion has been identified as a major cause of cardiopulmonary diseases. Briquette and charcoal are two representative processed fuels that exhibit different emission characteristics. This study compared three types of biomass fuels (maize straw, wheat straw, and wood branches) and their respective processed fuels in terms of their emission factors (EFs). The bioreactivity of human alveolar epithelial (A549) cells to exposure to various fuel-emitted PM2.5 was assessed. The EFs of lactic dehydrogenase (LDH) and interleukin-6 (IL-6) were calculated to compare actual cytotoxicity. The PM2.5 EFs of maize and wheat straw were higher than those of wood branches, and following the processes of briquetting and carbonization, the EFs of PM2.5 and chemical components were effectively reduced. Cell membrane damage and inflammatory responses were observed after A549 cell exposure to PM2.5 extracts. The expression of bioreactivity to briquettes and charcoals was lower than that to raw fuels. The EFs of LDH and IL-6 were also significantly reduced after briquetting and carbonization. This underscores the necessity of fuel treatment for reducing cytotoxicity. The crucial chemical components that contributed to cell oxidative and inflammatory responses were identified, including organic and elemental carbon, water-soluble ions (e.g., K+, Mg2+, and Ca2+), metals (e.g., Fe, Cr, and Ni), and high-molecular-weight PAHs. This study elucidated the similarities and differences of PM2.5 emissions and cytotoxicity of three types of biomass fuel and demonstrated the positive effects of fuel treatment on reducing adverse pulmonary effects.

Controlled air exchange rate method to evaluate reduction of volatile organic compounds by indoor air cleaners.

Air cleaning technologies are needed to reduce indoor concentrations and exposure to volatile organic compounds (VOCs). Currently, air cleaning technologies lack an accepted test standard to evaluate their VOC removal performance. A protocol to evaluate the VOC removal performance of air cleaning devices was developed and piloted with two devices. This method injects a VOC mixture and carbon dioxide into a test chamber, supplies outdoor air at a standard building ventilation rate, periodically measures the VOC concentrations in the chamber using solid phase microextraction-gas chromatography-mass spectrometry over a 3-h decay period, and compares the decay rate of VOCs to carbon dioxide to measure the VOC removal air cleaning performance. The method was demonstrated with both a hydroxyl radical generator and an activated carbon air cleaner. It was shown that the activated carbon air cleaner device tested had a clean air delivery rate an order of magnitude greater than the hydroxyl radical generator device (72.10 vs 6.32 m3/h).

Raw to charred: Changes of precursors and intermediates and their correlation with heterocyclic amines formation in grilled lamb.

This work aimed to investigate the changes and correlations of precursors, intermediates and heterocyclic amines (HCAs) in lamb during charcoal grilling. 28 chemical compounds were detected by high-performance liquid chromatography and gas chromatography-mass spectrometry in grilled lamb from raw to charred. Results demonstrated the types and contents of HCAs were increased during grilling, of which 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP) was dominant and accounted for 61% at the end of grilling (42 min). Glucose and creatine (P < 0.05) decreased with grilling time, creatinine (P < 0.05) and total free amino acid increased. The types and contents of four intermediates (formaldehyde, acetaldehyde, phenylacetaldehyde, 2,5-dimethylpyrazine) increased during grilling. Glucose, creatine, creatinine, ten free amino acids and four intermediates showed significant correlation to HCAs. Also, the ratios of four precursors were significantly correlated with HCAs (P < 0.05), besides creatine/glucose ratio. These results suggested that the time of charcoal grilling should not exceed 14 min at 145 °C in order to reduce the formation of harmful compounds in lamb meat.

Characterization of fine particulate matter from indoor cooking with solid biomass fuels.

Household burning of solid biomass fuels emits pollution particles that are a huge health risk factor, especially in low-income countries (LICs) such as those in Sub-Saharan Africa. In epidemiological studies, indoor exposure is often more challenging to assess than outdoor exposure. Laboratory studies of solid biomass fuels, performed under real-life conditions, are an important path toward improved exposure assessments. Using on- and offline measurement techniques, particulate matter (PM) from the most commonly used solid biomass fuels (charcoal, wood, dung, and crops residue) was characterized in laboratory settings using a way of burning the fuels and an air exchange rate that is representative of real-world settings in low-income countries. All the fuels generated emissions that resulted in concentrations which by far exceed both the annual and the 24-hour-average WHO guidelines for healthy air. Fuels with lower energy density, such as dung, emitted orders of magnitude more than, for example, charcoal. The vast majority of the emitted particles were smaller than 300 nm, indicating high deposition in the alveoli tract. The chemical composition of the indoor pollution changes over time, with organic particle emissions often peaking early in the stove operation. The chemical composition of the emitted PM is different for different biomass fuels, which is important to consider both in toxicological studies and in source apportionment efforts. For example, dung and wood yield higher organic aerosol emissions, and for dung, nitrogen content in the organic PM fraction is higher than for the other fuels. We show that aerosol mass spectrometry can be used to differentiate stove-related emissions from fuel, accelerant, and incense. We argue that further emission studies, targeting, for example, vehicles relevant for LICs and trash burning, coupled with field observations of chemical composition, would advance our understanding of air pollution in LIC. We believe this to be a necessary step for improved air quality policy.

Analysis of trace phytoavailable heavy metals in saline soil extract by one-step electroextraction coupled with in situ desorption microplasma optical emission spectrometry.

On-site and sensitive analysis of phytoavailable heavy metals is the key to fast evaluate the pollution incidents, while the development of convenient and efficient sample introduction approaches against matrix interference is crucial to improve the performances of field-deployable instruments. Herein, trace phytoavailable heavy metals in soil are first extracted by 0.1 M NaNO3, afterwards adsorbed onto an activated carbon tip via electroextraction (EE), and finally analyzed by dielectric barrier discharge (DBD) microplasma optical emission spectrometry (OES) via in situ desorption. The activated carbon tip is not only able to extract heavy metals from alkali metals/alkaline earth metals matrix, resisting the interference of coexisting anions and non-electroactive species in saline soil extract, but also significantly improves the detection sensitivity of subsequent DBD-OES analysis by increasing loading amounts of analytes. Taking the key heavy metals pollution as model, the detection limits of Cd, Zn, Cu and Pb reach 0.8, 2.3, 6.0 and 4.5 µg kg-1, respectively, and precisions are within 2.7-4.6%. The accuracy and practicability of the present miniaturized EE-DBD-OES device have been verified by measuring several certified reference materials and real soil samples, providing a promising tool for convenient and sensitive analysis of trace phytoavailable heavy metals in soil.