Cellulose-based thermosensitive supramolecular hydrogel for phenol removal from polluted water.

Pollution of phenolic effluent from spice and plastics factories has become increasingly serious. Thus, developing a green and highly efficient adsorbent to remove phenolic compounds from wastewater is of urgent need. In this study, cellulose graft copolymer was synthesized through grafting 4-vinylpyridine monomer and polyethylene glycol methacrylate to a molecular skeleton of cellulose by free radical polymerization. The supramolecular hydrogel was successfully synthesized by physical cross-linking of cellulose graft copolymer and α-cyclodextrin. These supramolecular hydrogels were thoroughly characterized and the adsorption performance (adsorption isotherms and adsorption kinetics) of phenol on the supramolecular hydrogel were investigated in batch operation. The supramolecular hydrogel not only exhibited excellent adsorption of phenol, but also demonstrated increased mechanical strength due to the introduction of a modified cellulose base material. The adsorption kinetics of phenol on the supramolecular hydrogel followed a quasi-second-order reaction, with a correlation coefficient of 0.9909. The adsorption isotherm conformed to the Langmuir adsorption isotherm, and the maximum adsorption capacity of phenol can reach 80.71 mg g-1, which was 2-3 times higher than traditional carbon-based materials. The results demonstrate the great promise of the waste-derived supramolecular hydrogel to be used as an efficient adsorbent in wastewater treatment.

Distance impacts toxic metals pollution in mining affected river sediments.

The study of metals mobility derived from mining activities in an ultramafic lithology is limited. This study investigates the effects of distance on potentially toxic metals such as Co, Cu, Fe, Mn, Ni, Pb, and Zn pollution, and the geochemical processes of fluvial system downstream of an ex-copper mine (Mamut River). The toxicity level of the river was evaluated using various sediment quality guidelines, ecotoxicological risks (ecological risk and risk index) and pollution indices. The geochemical behavior and stability of these toxic metals in the solid-phase samples were also examined. The results show that elevated concentrations of Ni, Cu, and Fe in the sediments can be linked to the adsorption and precipitation of metals from the aqueous-phase samples. We found that the metal scavenging rate as a function of distance is more evident in tropical environments than it was previously thought (10 km downstream). Such an inference could be explained by the greater amount of rainfall (pH 5.5-6.5) received in the tropics and higher weathering products that could react and form stable complexes. Geochemical analysis of the river sediment indicates that Ni, Cu, and Fe in the river sediment have increased 44-, 81-, and 90-fold compared to the background values, respectively. A significant decrease in the concentration of the potentially toxic metals was found at 5.5 km downstream. The scavenging rate of Fe is the highest (1485.82 µg g-1 km-1) followed by Cu (141.48 µg g-1 km-1), Ni (10.23 µg g-1 km-1), Pb (8.12 µg g-1 km-1) and Zn (5.01 µg g-1 km-1) in the tropical river system. In contrast, the concentration of Co and Mn in the river sediments doubled as the river flows approximately 5 km downstream due to the higher mineral solubility and weaker metal partition coefficient. This study also discusses the possibility of asbestos (mainly as chrysotile in the X-ray diffraction) as a potential hidden risk present within the ultramafic setting. This case study can be extrapolated to explain the dispersion of inorganic pollutants in an ultramafic environment in a global context.

Assessment of heavy metals contamination in Mamut river sediments using sediment quality guidelines and geochemical indices.

This paper describes the concentration of selected heavy metals (Co, Cu, Ni, Pb, and Zn) in the Mamut river sediments and evaluate the degree of contamination of the river polluted by a disused copper mine. Based on the analytical results, copper showed the highest concentration in most of the river samples. A comparison with Interim Canadian Sediment Quality Guidelines (ICSQG) and Germany Sediment Quality Guidelines (GSQG) indicated that the sediment samples in all the sampling stations, except Mamut river control site (M1), exceeded the limit established for Cu, Ni, and Pb. On the contrary, Zn concentrations were reported well below the guidelines limit (ICSQG and GSQG). Mineralogical analysis indicated that the Mamut river sediments were primarily composed of quartz and accessory minerals such as chalcopyrite, pyrite, edenite, kaolinite, mica, and muscovite, reflected by the geological character of the study area. Enrichment factor (EF) and geoaccumulation index (Igeo) were calculated to evaluate the heavy metal pollution in river sediments. Igeo values indicated that all the sites were strongly polluted with the studied metals in most sampling stations, specifically those located along the Mamut main stream. The enrichment factor with value greater than 1.5 suggested that the source of heavy metals was mainly derived from anthropogenic activity such as mining. The degree of metal changes (δfold) revealed that Cu concentration in the river sediments has increased as much as 20 to 38 folds since the preliminary investigation conducted in year 2004.

Modeling aerosol transmission of SARS-CoV-2 from human-exhaled particles in a hospital ward.

The COVID-19 pandemic has plunged the world into uncharted territory, leaving people feeling helpless in the face of an invisible threat of unknown duration that could adversely impact the national economic growths. According to the World Health Organization (WHO), the SARS-CoV-2 spreads primarily through droplets of saliva or discharge from the mouth or nose when an infected person coughs or sneezes. However, the transmission of the SARS-CoV-2 through aerosols remains unclear. In this study, computational fluid dynamic (CFD) is used to complement the investigation of the SARS-CoV-2 transmission through aerosol. The Lagrangian particle tracking method was used to analyze the dispersion of the exhaled particles from a SARS-CoV-2-positive patient under different exhale activities and different flow rates of chilled (cooling) air supply. Air sampling of the SARS-CoV-2 patient ward was conducted for 48-h measurement intervals to collect the indoor air sample for particulate with diameter less than 2.5 µm. Then, the reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) was conducted to analyze the collected air sample. The simulation demonstrated that the aerosol transmission of the SARS-CoV-2 virus in an enclosed room (such as a hospital ward) is highly possible.

Particulate matter (PM2.5) as a potential SARS-CoV-2 carrier.

The rapid spread of the SARS-CoV-2 in the COVID-19 pandemic had raised questions on the route of transmission of this disease. Initial understanding was that transmission originated from respiratory droplets from an infected host to a susceptible host. However, indirect contact transmission of viable virus by fomites and through aerosols has also been suggested. Herein, we report the involvement of fine indoor air particulates with a diameter of ≤ 2.5 µm (PM2.5) as the virus's transport agent. PM2.5 was collected over four weeks during 48-h measurement intervals in four separate hospital wards containing different infected clusters in a teaching hospital in Kuala Lumpur, Malaysia. Our results indicated the highest SARS-CoV-2 RNA on PM2.5 in the ward with number of occupants. We suggest a link between the virus-laden PM2.5 and the ward's design. Patients' symptoms and numbers influence the number of airborne SARS-CoV-2 RNA with PM2.5 in an enclosed environment.

The microbially driven formation of siderite in salt marsh sediments.

We employ complementary field and laboratory-based incubation techniques to explore the geochemical environment where siderite concretions are actively forming and growing, including solid-phase analysis of the sediment, concretion, and associated pore fluid chemistry. These recently formed siderite concretions allow us to explore the geochemical processes that lead to the formation of this less common carbonate mineral. We conclude that there are two phases of siderite concretion growth within the sediment, as there are distinct changes in the carbon isotopic composition and mineralogy across the concretions. Incubated sediment samples allow us to explore the stability of siderite over a range of geochemical conditions. Our incubation results suggest that the formation of siderite can be very rapid (about two weeks or within 400 hr) when there is a substantial source of iron, either from microbial iron reduction or from steel material; however, a source of dissolved iron is not enough to induce siderite precipitation. We suggest that sufficient alkalinity is the limiting factor for siderite precipitation during microbial iron reduction while the lack of dissolved iron is the limiting factor for siderite formation if microbial sulfate reduction is the dominant microbial metabolism. We show that siderite can form via heated transformation (at temperature 100°C for 48 hr) of calcite and monohydrocalcite seeds in the presence of dissolved iron. Our transformation experiments suggest that the formation of siderite is promoted when carbonate seeds are present.

Characterization of rainwater chemical composition after a Southeast Asia haze event: insight of transboundary pollutant transport during the northeast monsoon.

Open biomass burning in Peninsula Malaysia, Sumatra, and parts of the Indochinese region is a major source of transboundary haze pollution in the Southeast Asia. To study the influence of haze on rainwater chemistry, a short-term investigation was carried out during the occurrence of a severe haze episode from March to April 2014. Rainwater samples were collected after a prolonged drought and analyzed for heavy metals and major ion concentrations using inductively coupled plasma mass spectroscopy (ICP-MS) and ion chromatography (IC), respectively. The chemical composition and morphology of the solid particulates suspended in rainwater were examined using a scanning electron microscope coupled with energy-dispersive X-ray spectroscopy (SEM-EDS). The dataset was further interpreted using enrichment factors (EF), statistical analysis, and a back trajectory (BT) model to find the possible sources of the particulates and pollutants. The results show a drop in rainwater pH from near neutral (pH 6.54) to acidic (