Despite being a key Malaysian economic contributor, the oil palm industry generates a large quantity of environmental pollutant known as palm oil mill effluent (POME). Therefore, the need to remediate POME has drawn a mounting interest among environmental scientists. This study has pioneered the application of Meyerozyma guilliermondii with accession number (MH 374161) that was isolated indigenously in accessing its potential to degrade POME. This strain was able to treat POME in shake flask experiments under aerobic condition by utilising POME as a sole source of carbon. However, it has also been shown that the addition of suitable carbon and nitrogen sources has significantly improved the degradation potential of M. guilliermondii. The remediation of POME using this strain resulted in a substantial reduction of chemical oxygen demand (COD) of 72%, total nitrogen of 49.2% removal, ammonical nitrogen of 45.1% removal, total organic carbon of 46.6% removal, phosphate of 60.6% removal, and 92.4% removal of oil and grease after 7 days of treatment period. The strain also exhibited an extracellular lipase activity which promotes better wastewater treatment. Additionally, Fourier transform infrared spectroscopy (FTIR) and gas chromatography-mass spectrometry (GC-MS) analyses have specifically shown that M. guilliermondii strain can degrade hydrocarbons, fatty acids, and phenolic compounds present in the POME. Ultimately, this study has demonstrated that M. guilliermondii which was isolated indigenously exhibits an excellent degrading ability. Therefore, this strain is suitable to be employed in the remediation of POME, contributing to a safe discharge of the effluent into the environment.

Two-line ferrihydrite (2LFh) was aged for 12 years under ambient conditions and sheltered from light in the presence of Lu(III) used as surrogate for trivalent actinides. 2LFh aging produced hematite rhombohedra with overgrown acicular goethite particles. Analysis of the homogeneous suspension by asymmetrical flow field-flow fractionation (AsFlFFF) coupled to ICP-MS indicated that particles have a mean hydrodynamic diameter of about 140 nm and the strong correlation of the Fe and Lu fractograms hinted at a structural association of the lanthanide with the solid phase(s). Unfortunately, recoveries were low and thus results cannot be considered representative of the whole sample. The suspension was centrifuged and X-ray absorption spectroscopy (XAS) at the Lu L₃-edge on the settled particles indicated that Lu(III) is sixfold coordinated by oxygen atoms, pointing to a retention by structural incorporation within particles. This result is consistent with AsFlFFF results on the same suspension without centrifugation. The detection of next nearest Fe and O atoms were consistent with the structure of goethite, ruling out incorporation within hematite. After centrifugation of the suspension, only nanoparticulate needle-like particles, very likely goethite, could be detected in the supernatant by ESEM. AsFlFFF data of the supernatant were comparable to that obtained for the homogeneous suspension, whereas XAS indicated that Lu(III) is predominantly present as dissolved species in the supernatant. Results from both techniques can be interpreted as a major fraction of Lu present as aqueous ions and a minor fraction as structurally incorporated. Findings from this study are corroborated by STEM-HAADF data and results from DFT calculations in a companion paper.

The management and remediation of abandoned hydrocarbon-contaminated sites require detailed information on the distribution of contaminant plumes. In areas where groundwater is active, the formation of contaminant plumes is associated with hydrodynamics, the nature of the sedimentary layers, and the nature of the pollutants and the degradation process. A comprehensive survey is needed to determine this information. An abandoned hydrocarbon disposal site is located in an area where groundwater is very active. In the investigation of contaminant plumes, we combined the geophysical method with accurate geochemical analysis of subsoil and groundwater samples. Ground-penetrating radar and electrical resistivity tomography images of the electrical anomalies potentially originating from hydrocarbon pollution were used to select sites for subsurface sampling. Total petroleum hydrocarbons, total dissolved solids, and groundwater pH were measured. The results showed that the source zone had undergone long-term natural attenuation, and it was unable to continuously output organic matter to support the expansion of contaminant plumes. Low-resistivity anomalies and enhanced attenuation in the study area were caused by hydrocarbon degradation products and enhanced mineral weathering. Delineating the distribution of contaminant plumes in areas where the resistivity was below 15 Ω m. The distribution of the plume in the vertical direction was related to the hydrocarbon release history (release rate and volume) and was affected by fluctuations in the groundwater level. The contaminant plume moved very slowly along the direction of the hydraulic gradient and was in a basically stable state. The results showed that the combined application of the geoelectrical method and the geochemical method can effectively describe the distribution of underground contaminant plumes in an aged pollution site.

The effects of low-molecular-weight organic acids (LMWOAs) on the transport of graphene oxide nanoparticles in saturated kaolinite- and goethite-coated sand columns were studied. Acetic acid, glycolic acid, malonic acid, and tartaric acid were chosen in the experiments. LMWOAs enhanced the mobility of GO by electrostatic/steric repulsion. In addition, they competed with GO for limited deposition sites on grain surfaces. The effects of organic acids on the transport of GO strongly depended on organic acid species. In general, the transport enhancement effects followed the order of tartaric acid > malonic acid > glycolic acid > acetic acid; this difference may be related to the number and type of functional groups of organic acids. Different LMWOAs enhanced the transport of GO in goethite-coated sand to a larger extent than did in kaolinite-coated sand under the test conditions; this was likely related to the differences of physicochemical characteristics between goethite and kaolinite. Organic acids significantly inhibited the deposition of GO at 0.5 mM Ca²⁺; this was possible that Ca²⁺ enhanced adsorption of organic acids by complexing with the surface O-functionalities of both LMWOAs and sand grain. Consequently, more organic acid molecules competed with GO for deposition sites on grain surfaces. Additionally, a two-site transport model was used to fit the transport data. Our findings have important implications for the understanding of the deposition and fate of GO in soil especially in rhizosphere environments where various low-molecular-weight organic acids are active.

Adsorption is a typical method for air pollutant removal from flue gas. A CuS-modified active coke (CuS/AC) sorbent was developed to improve the elemental mercury removal efficiency from municipal solid waste incineration (MSWI) flue gas. The influences of the loading amount of CuS, reaction temperature, and flue gas components including O₂, SO₂, H₂O, and HCl on Hg⁰ removal efficiency were investigated, respectively. The results showed that the mercury adsorption capacity of CuS/AC₍₂₀%₎ sorbent was about 7.17 mg/g with 50% breakthrough threshold, which is much higher than that of virgin active coke. The analysis of XPS indicated that HgS was the main species of mercury on spent CuS/AC, which implied that adsorption and oxidation were both included in Hg⁰ removal. S₂²⁻ played a vital role in the oxidation of physically adsorbed Hg⁰. Meanwhile, the common components of MSWI flue gas exhibited no significant inhibition effect on Hg⁰ removal by CuS/AC sorbent. CuS/AC sorbent is a promising sorbent for the mercury removal from MSWI flue gas.

The biotoxicity of heavy metals in sediments toward benthic organisms has evoked great concern for the health of freshwater ecosystems. This study applied a sediment toxicity testing protocol to investigate the single and joint toxicity of cadmium (Cd) and lead (Pb) on Bellamya aeruginosa. B. aeruginosa were exposed to different concentrations of Cd (5, 25, and 100 mg/kg), Pb (20, 100, and 400 mg/kg), and their different concentration combinations. A suite of biomarkers, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), metallothionein (MT), malondialdehyde (MDA), and acetylcholinesterase (AChE), were measured after 7, 14, 21, and 28 days of exposure to evaluate their oxidative stress status. Cell apoptosis of soft tissue was also determined after exposure. Results revealed that these endpoints represented sensitive biomarkers for the characterization of the oxidative stress response induced by these metals. Specifically, a decrease of SOD and GPx and an increase of MDA were indicative of the potential failure of the antioxidant defense system in neutralizing the reactive oxygen species (ROS) generated in the exposure of the Pb-treated group. The integrated biomarker response (IBR) index revealed the most significant sub-lethal toxicity for Pb-spiked sediments, leading to the highest rate of cell apoptosis (70.8%). Exposure to Cd resulted in a time- and dose-dependent effect on MT levels, which suggested active detoxification of this metal. Exposure to the mixture resulted in amelioration of Pb toxicity, likely due to the competitive binding of Cd to active enzyme, with the result of an observed antagonistic interaction. This study indicated that B. aeruginosa represents a good biomonitor for assessing Cd and Pb contamination of sediments, and laid the foundation for their potential risk assessments in freshwater ecosystems.

An important aspect of the regulatory process is the performance comparison of regulated firms. This exists in regulated industries where tariffs are determined through a benchmarking process such as the English and Welsh water industry. A double-bootstrap data envelopment analysis (DEA) approach was applied to overcome the uncertainty in efficiency scores and to reveal the influence of environmental variables on 18 water companies in England and Wales during the 2001–2016 period. The results showed that bias and bias-corrected efficiency scores lead to changes in the water companies’ rankings. This reveals the importance of using reliable methodologies to support the decision-making process. Higher levels of average pumping head, leakage, and abstraction of water from reservoirs lead to lower efficiency. In contrast, increased population density leads to larger efficiency. We also link the results from the efficiency of water companies with the regulatory cycle. Our findings can be useful to policy makers for them to better understand water utilities’ performance and to aid them in reshaping their current policies and practices to improve efficiency and provide better service to customers.

A rapid and sensitive immunoassay for the simultaneous detection of imidacloprid and thiacloprid was developed by using magnetic nanoparticles (MNPs) and upconversion nanoparticles (UCNPs). The UCNPs of NaYF₄:Yb, Er and NaYF₄:Yb, Tm were synthesized and conjugated with anti-imidacloprid monoclonal antibody (mAb) and anti-thiacloprid mAb as signal labels, while the MNPs were conjugated with antigens of thiacloprid and imidacloprid as separation elements. The fluorescence intensities of Yb/Er- and Yb/Tm-doped UCNPs were detected simultaneously in 544 nm and 477 nm under the excitation of NIR light (980 nm). The amounts of mAb-conjugated UCNPs that were separated by antigen-conjugated MNPs were determined based on competitive immunoassays. Under the optimal conditions, the 50% inhibiting concentration (IC₅₀) and limit of detection (LOD, IC₁₀) were 5.80 and 0.32 ng/mL for imidacloprid and 6.45 and 0.61 ng/mL for thiacloprid, respectively. The immunoassay exhibited negligible cross-reactivity with analogs of imidacloprid and thiacloprid except imidaclothiz (86.2%). The average recoveries of imidacloprid and thiacloprid in environmental and agricultural samples, including paddy water, soil, pears, oranges, cucumbers, and wheat, ranged from 78.4 to 105.9% with relative standard deviations (RSDs) of 2.1–11.9% for imidacloprid and ranged from 82.5 to 102.3% with RSDs of 1.0–16.5% for thiacloprid. In addition, the results of the immunoassay correlated well with high-performance liquid chromatography for the detection of the authentic samples.

Amine-modified diatomite with remarkable formaldehyde (HCHO) removal efficiency was prepared by grafting 3-aminopropyltrimethoxysilane (APTMS) in this research. The interfacial properties and microstructures of the prepared adsorbents were characterized and analyzed. The HCHO adsorption properties of the amine modified diatomite were also systematically studied, and it has been proven to be effective adsorbent with better adsorption performance than activated carbon for the removal of gaseous HCHO. Furthermore, to better explain the experimental results, we performed density functional theory (DFT) study on the adsorption system and calculated the geometry, energy, and charge parameters based on first principles. Also, the underlying adsorption mechanism was proposed detailedly by combining experimentation with DFT calculation, suggesting that amine modified diatomite can be efficient adsorbent for the elimination of gaseous formaldehyde.

Biosorption potential of oxidised coconut coir (OCC) for removal of Cd(II) was evaluated by multi-column arrangement by connecting three columns in series. Effect of flow rate at 5, 10 and 15 mL/min was studied at 30 mg/L initial Cd(II) concentration. The dynamic capacity of the system was found to be 321, 206 and 83 mg/L for 5, 10 and 15 mL/min flow rates, respectively, by applying the bed depth service time model. Biosorbent usage rates for single-column and multi-column systems were compared. Better utilisation of biosorbent was observed when the columns are connected in series at similar operating parameters. A simple acid-base regeneration procedure was found to be effective in desorbing/regenerating the cadmium bound biosorbent. Adsorption efficiency was found to decrease from 76.3% for the first cycle to 72.2% and 70.6% in the second and third cycles, respectively. Regeneration efficiencies were more than 94% up to 3 cycles. The study highlights the effectiveness of the multi-column system in biosorption against the conventional single-column system.