This study determined the contamination levels of oil and grease (O/G) across nine (9) galamsey operations under different environmental media (background soil, surface drainage, slurry/sludge and galamsey wastes) in three galamsey hotspot assemblies (Tarkwa Nsuaem, Amenfi East and Prestea Huni Valley) within the Western region of Ghana. Triplicate samples each of the four environmental media for the nine galamsey types (Washing Board, Washing Plant, Anwona, Dig and Wash, Dredging, Underground Abandoned Shaft, Underground Sample Pit, Chamfi and Mill House) were collected and analysed using n-hexane extractable materials in acidic medium by extraction and gravimetry to determine O/G concentrations. From the comparison of mean ranked concentration of O/G, using Kruskal-Wallis Test, the observed differences in the ranking was significant across all four media. The O/G concentrations for Anwona, Chamfi, Mill House, Washing Board and Washing Plant galamsey recorded exceedances when compared to the Ghana EPA Effluent Guideline Value of 100 mg/L for water and The New Dutch Lists’ Target and Intervention Value of 50 mg/kg and 500 mg/kg for solid/semi-solid materials. Consistently and for all environmental media types, the levels of O/G across the galamsey types were in the descending order of: Washing Board, Chamfi, Anwona, Mill House, Washing Plant, Underground Sample Pit, River Dredging, Dig and Wash, Underground Abandoned Shaft and Control Sample (non-galamseyed areas). In general, the surface drainage medium was predominantly found to be the most impacted upon medium from hydrocarbons by seven of the nine galamsey operations (Washing Board, Anwona, Chamfi, Mill House, Dredging, Dig and Wash and Underground Sample Pit). This was followed by slurry/sludge, background soil and waste media in that order. Expectedly, there were no exceedances for the Reference or Control Samples (non-galamseyed areas).

Low-cost, light-scattering-based particulate matter (PM) sensors are becoming more widely available and are being increasingly deployed in ambient and indoor environments because of their low cost and ability to provide high spatial and temporal resolution PM information. Researchers have begun to evaluate some of these sensors under laboratory and environmental conditions. In this study, a low-cost, particulate matter sensor (Plantower PMS 1003/3003) used by a community air-quality network is evaluated in a controlled wind-tunnel environment and in the ambient environment during several winter-time, cold-pool events that are associated with high ambient levels of PM. In the wind-tunnel, the PMS sensor performance is compared to two research-grade, light-scattering instruments, and in the ambient tests, the sensor performance is compared to two federal equivalent (one tapered element oscillating microbalance and one beta attenuation monitor) and gravimetric federal reference methods (FEMs/FRMs) as well as one research-grade instrument (GRIMM). The PMS sensor response correlates well with research-grade instruments in the wind-tunnel tests, and its response is linear over the concentration range tested (200–850 μg/m³). In the ambient tests, this PM sensor correlates better with gravimetric methods than previous studies with correlation coefficients of 0.88. However additional measurements under a variety of ambient conditions are needed. Although the PMS sensor correlated as well as the research-grade instrument to the FRM/FEMs in ambient conditions, its response varies with particle properties to a much greater degree than the research-grade instrument. In addition, the PMS sensors overestimate ambient PM concentrations and begin to exhibit a non-linear response when PM2.5 concentrations exceed 40 μg/m³. These results have important implications for communicating results from low-cost sensor networks, and they highlight the importance of using an appropriate correction factor for the target environmental conditions if the user wants to compare the results to FEM/FRMs.

The cationic degradable polymer poly(lactic acid) choline iodide ester methacrylate, poly(PLA₄ChMA), can be used to flocculate particles and dewater sediments from tailings ponds and wastewater. A suitable bioaccessibility method is required to characterize the interactions of this novel flocculant in the human gastrointestinal system. To this end, a physiologically based extraction test (PBET) was modified to evaluate the bioaccessibility of flocculants. Bioaccessibility (bioaccessible fraction) is a measure of the solubility of a contaminant in gastrointestinal fluids and that may be available for systemic absorption. The flocculants poly(PLA₄ChMA), SNF C3276, and FLOPAM A3338 were tested at a solid-to-liquid ratio of 1:200 in the absence and presence of kaolin clay, which is used as a model sediment compound. Bioaccessible fractions were characterized by proton nuclear magnetic resonance spectroscopy and estimated by gravimetry. The bioaccessibility of poly(PLA₄ChMA) in gastric and intestinal PBET solutions decreases from 78% and 100%, respectively, in the absence of kaolin to approximately 0% with kaolin, indicating that poly(PLA₄ChMA) remains adsorbed onto the clay surface throughout the PBET, a result confirmed by thermogravimetric analysis. The bioaccessibility of cationic SNF C3276 and anionic FLOPAM A3338 in gastric solution is approximately 76% and 26%, respectively, and is not affected by the presence of kaolin. However, in intestinal solutions, the bioaccessibility of SNF C3276 and FLOPAM A3338 (60–85% in the absence of kaolin) changes to 0% and 100%, respectively, in the presence of kaolin. These results, interpreted in terms of solution pH and surface charge, demonstrate that interactions with kaolin influence the solubility of flocculants and must be considered in the evaluation of bioaccessibility. In future works, such bioaccessibility methods can be applied to assess the human-health safety of using flocculants in wastewater treatments.

Fish meal (FM) is an industrial product, mainly obtained from whole wild-caught fish, that is used as a high protein feedstuff component in aquaculture and intensive animal farming. Contamination of FM by microplastics (MPs), the synthetic polymer particles known to be nearly ubiquitous in the marine environment, is a likely consequence of their ingestion by zooplankton and other small marine animals that through the food chain end up in the fish commercialized not only for direct human consumption but also for the industrial production of FM. Unfortunately, analytical tools for quantifying contamination of FM by synthetic polymers are not available. A newly developed procedure described here allows quantification of the total amounts of polyolefins (including ethene and propene homo- and copolymers), polystyrene (PS), and poly(ethylene terephthalate) (PET), respectively, in FM. The multi-step procedure involves a sequence of solvent extractions, hydrolytic treatments to remove the biogenic matrix mainly consisting of proteins and some lipids, and selective depolymerization for PET. The gravimetric and SEC-UV techniques employed for the quantification of polyolefins and PS, respectively, only allowed to estimate their concentration in FM at around or below 100 mg/kg each, a more accurate quantification being prevented by the interference from the organic matrix and, in the case of polyolefins, by the limited sensitivity of the quantification by gravimetry. On the other hand, the contamination by PET MPs could accurately be quantified at 12.9 mg/kg based on the dry FM mass. Ways to overcome the sensitivity limitations for PS and polyolefins by using e.g. pyrolysis-GC/MS are highlighted.

Ambient fine particulate matter (PM2.5) pollution has been implicated in the development of hypertensive disorders of pregnancy. However, evidence on the effects of PM2.5-derived chemical constituents on gestational blood pressure (BP) is limited, and the potential mechanisms underlying the association remain unclear. In this study, we repeated three consecutive 72-h personal air sampling and BP measurements in 215 pregnant women for 590 visits during pregnancy. Individual PM2.5 exposure level was assessed by gravimetric method and 28 PM2.5 chemical constituents were analyzed by ED-XRF method. Plasma biomarkers of endothelial function and inflammation were measured using multiplexed immunoassays. Robust multiple linear regression models were used to estimate the associations among personal PM2.5 exposure and chemical constituents, BP changes (compared with pre-pregnancy BP) and plasma biomarkers. Mediation analyses were performed to evaluate underlying potential pathways. Result showed that exposure to PM2.5 was significantly associated with increases in systolic blood pressure (SBP), diastolic blood pressure (DBP) and mean arterial pressure (MAP) in the early second trimester. Meanwhile, elevated concentration of lead (Pb) constituent in PM2.5 was significant associated with increases in DBP and MAP after adjusting for PM2.5 total mass. PM2.5 and Pb constituent also presented positive associations with plasma biomarkers of endothelial function (ET-1, E-selectin, ICAM-1) and inflammation (IL-1β, IL-6, TNFα) significantly. After multiple adjustment, elevated ET-1 and IL-6 were significantly correlated with increased gestational BP, and respectively mediated 1.24%–25.06% and 7.01%–10.69% of the increased BP due to PM2.5 and Pb constituent exposure. In conclusion, our results suggested that personal exposure to PM2.5 and Pb constituent were significantly associated with increased BP during pregnancy, and the early second trimester might be the sensitive window of PM2.5 exposure. The endothelial dysfunction and elevated inflammation partially mediated the effect of PM2.5 and Pb constituent on BP during pregnancy.

Microplastics (MPs) are contaminants of environmental concern that represent a threat to marine systems. Here we report data on the abundance and characteristics of MPs collected from surface waters of the urban Guanabara Bay. Samples were collected, by horizontal trawling of a plankton net on two occasions (summer of 2016). The MPs were obtained from samples by sieving and particles were manually sorted with microscope. Characterization of MPs was accomplished by gravimetry and digital image processing (for quantification and morphology categorization), and chemical composition identified by infrared spectroscopy and elemental analyses. Total MPs ranged from 1.40 to 21.3 particles/m3, which places Guanabara Bay amongst the most contaminated coastal systems worldwide by microplastics. Polyethylene and polypropylene polymers ≤1 mm were the most abundant particles. Therefore, the occurrence of MPs in Guanabara Bay is relevant to understand ecological hazards of exposition to marine biota and merits further investigation.

The indigenous oil-degrading bacterial consortia MARA and MARB were enriched from the deep-sea sediments of South Mid-Atlantic Ridge (MAR) with crude oil as sole carbon and energy sources. Biodiversity and community analyses showed that members of α-Proteobacteria were the key players in consortium MARA, whereas those of γ-Proteobacteria were the key players in consortium MARB, which were studied by MiSeq sequencing method. Gravimetric method estimated the oil degradation rates of MARA and MARB to be 63.4% and 85.8%, respectively, after 20d. Eleven cultivable oil degraders with different morphologies were isolated. These strains were identified as Alcanivorax, Bacillus, Dietzia, Erythrobacter, Marinobacter, Nitratireductor, and Oceanicola based on 16S rRNA gene sequences. Three strains belonging to Dietzia exhibited the highest oil degradation capability. Results indicated that the intrinsic biodegradation capacity of oil contaminants by indigenous microbial communities exists in South MAR sediments.

The mass concentrations and content of water-soluble anions (Cl⁻, NO₃⁻, SO₄²⁻) and cations (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺) in the PM₂.₅ particle fraction were measured, and an investigation of their relationship and their contribution to the total PM₂.₅ mass measured was conducted at an urban background site as part of the Croatian monitoring network for air quality located in Rijeka, Croatia. Daily samples of PM₂.₅ particle fraction were collected over 2017 on PTFE filters using a low volume sampler Sven Leckel SEQ 47/50. Mass concentrations of the PM₂.₅ particle fraction were determined by gravimetry according to the standard HRN EN 12341:2014 (EN 12341:2014). The content of water-soluble inorganic anions and cations were determined using a Thermo Scientific ICS-5000 capillary ion chromatograph. Results show that the annual average PM₂.₅ mass concentration was 9.65 μg m⁻³ and did not exceed the limit value of 25 μg m⁻³ given by the Regulation on the level of pollutants in air (OG No. 117/12). The annual average mass concentrations of ions in PM₂.₅ particle fraction was SO₄²⁻> NH₄⁺> NO₃⁻ > Ca²⁺> K⁺> Na⁺> Cl⁻ > Mg²⁺. The contributions of total anion mass and total cation mass to the total PM₂.₅ mass were 25.4% and 12.8%, respectively. The acidic property of PM₂.₅ was obtained in spring and winter and slightly acidic in summer and autumn. For a prediction of the pollutant sources, we ran a factor analysis which was performed using the statistical packages STATISTICA 13.0. After varimax rotation, the obtained four principal component factors were found to account for 86% of the variance. Factor loadings > 0.7 were considered significant.

Total petroleum hydrocarbons (TPH) is an important parameter for evaluating risk and establishing cleanup requirements at petroleum release sites. However, different analytical methods may provide incomparable results. To select more appropriate method and design cost-effective remediation strategy, a comparison study of four analytical methods (gravimetric method, infrared spectrometry (IR), gas chromatography-flame ionization detection (GC-FID), and ultraviolet spectrophotometer (UV)) is conducted for soil samples spiked by crude oil and fuel oils under both non-weathered and short-term weathered conditions. The gravimetric method produces higher TPH recovery for less volatile samples such as samples contaminated by motor oil and crude oil. The UV method reports very low TPH recovery and thus fails to provide the meaningful results in all tested samples. The IR method is a quick and relatively inexpensive screening tool and generally gives high TPH recovery, but the method precision and reproducibility are relatively low. The GC-FID method is relatively expensive and time consuming, but it has several advantages: (1) is more selective to hydrocarbons; (2) the method precision and reproducibility is relatively high; (3) is able to provide chemical fingerprint information. Therefore, appropriate method and should be chosen carefully depending on oil contamination type and investigation purpose. The results of short-term simulated weathering experiment showed 99.6% and 65.3% of TPH measured by the GC-FID method were removed for the kerosene and diesel contaminated soils after 14 days of weathering at 50ºC, respectively. We have provided evidence that weathering is an important attenuation pathway at kerosene and diesel spill sites. We can design the most cost-effective remediation strategy according to different oil types spilled.

Phthalic acid ester (PAE), a plasticizer, is increasingly being detected in different environments. These compounds can gravely affect the human endocrine system. The present study aims to prepare adsorbents that can effectively adsorb PAE pollutants. To fabricate a better carbon structure than conventional biochar, the sodium hydroxide solution was used as a hydrolyzing agent to pretreat the biomass in order to weaken the bonds in lignin, cellulose, and hemicellulose. As a result, biochar with a special porous carbon structure is obtained. To study the characteristics of the biochar and its adsorption properties, dimethyl phthalate (DMP)—a PAE—was selected as the adsorbate. The morphology and structural composition of the biochar were examined via an environment scanning electron microscope with a field emission gun (SEM), surface area analyzer (BET), Fourier transform infrared spectrometer (FTIR), thermal gravimetry (TG/DTG), X-ray diffractometry (XRD), and Raman spectroscopy. The BET data of the biochar increased by 125.3 times than that of the original biochar. The layer spacing and the surface functional groups of the pretreated biochar also increased. After performing the micro-morphological regulation of biomass using sodium hydroxide, the adsorption performance of biochar with regard to PAE effectively improved and an adsorption capacity of 125 mg/g was observed for DMP. The adsorption kinetics and thermodynamic experiments showed that DMP adsorption by biochar follows the Langmuir and pseudo-second-order models.