To remove phosphate from solution, a new class of sorbent based on chitosan bead (CB) was prepared using copper ion (Cu(II)) with/without a traditional crosslinking agent (glutaraldehyde [GLA]); these materials are referred to as CB-G-Cu and CB-Cu, respectively. Copper ions play a key role in the CB synthesis; these species crosslink each polymer chain, and during phosphate removal, they are the active functional group. Overall, 2.5 % (w/w) of chitosan is necessary to maintain the physical properties of the bead. In the FTIR spectra, adding GLA decreased the intensity of the amino group in chitosan, lowering the amount of copper in the CB. The maximum phosphate uptake (Q) for CB-Cu was 53.6 mg g⁻¹when calculated with the Langmuir isotherm, and the phosphate equilibrium was achieved in 12 h. Although the solution pH was not strongly affected, values below 7 are optimal for phosphate removal. The CB-Cu can be feasibly applied during a fixed column test, revealing that the phosphate breakthrough was 1.5 times higher than with CB-G-Cu.

The Park River watershed (PRW), a sub-basin of the Lower Connecticut River watershed, has experienced increased urbanization over the last century as the city of Hartford and its surrounding towns have grown and developed. We present watershed-wide and outflow scale maps of the trace metals Cd, Cu, Zn, and Pb to determine patterns of contamination in fine (<63 μm) stream sediment. Results are compared to established sediment quality guidelines (SQG) and probable effect concentrations (PEC) for each metal. Throughout the watershed, higher concentrations of trace metals are observed in the more urbanized south branch of the PRW. In this sub-basin, there are more industries that use, and waste, metals in their manufacturing processes that contribute to acutely high concentrations of metals in the fine bedload sediments. Impervious surfaces are examined as well in the context of the entire watershed. While an increase in metals can be attributed to an increase in impervious surfaces, these increases do not generally exceed SQGs and PECs. Two focused mapping studies were conducted at the storm water outflow of the West Hartford Landfill and the Trout Brook Sanitary Sewer Overflow (SSO). The purpose of these studies was to analyze the local effects of natural stream features such as channel bar deposits next to the outfalls. We determined that the sediment directly below the two outfalls often exceeded the PEC, while the accumulated sediment around the channel bar deposits was not contaminated beyond background stream levels. We believe mapping at both the small (watershed) and large (outfall) scale can be helpful in future urban studies to determine the extent of trace metal sediment contamination in both channelized and natural sections and may provide a useful method for sediment mitigation endeavors.

Groundwater is the principal source of drinking water for at least one third of Earth’s human inhabitants. Thus, protection of groundwater is a critical issue in many locales. Nitrates and other contaminants that impact human health are of particular concern. Mapping of aquifer vulnerability to pollution is a critical first step in implementing groundwater management protection programs; however, mapping is often constrained by generalizations inherent in model formulation and availability of data. In this study, a groundwater vulnerability model, which employs data extracted from widely available national and statewide geospatial datasets, is used to evaluate regional groundwater pollution risk in the Elkhorn River Basin, Nebraska, USA. The model, implemented in a geographic information system (GIS), is specifically structured to address risks of nitrate contamination in agricultural landscapes; thus, land use is a key factor. Modeled groundwater vulnerability was found to be positively correlated with nitrate concentrations obtained from sampled wells. The results suggest that the approach documented here could be used effectively to model regional groundwater pollution risk in other areas.

Air pollution contributes substantially to global health burdens; however, less is known about pollution patterns in China and whether they differ from those elsewhere. We evaluated temporal and spatial heterogeneity of air pollution in Lanzhou, an urban Chinese city (April 2009–December 2012), and conducted a systematic review of literature on air pollution and health in Lanzhou. Average levels were 141.5, 42.3, and 47.2 μg/m³for particulate matter with an aerodynamic diameter ≤10 μm (PM₁₀), NO₂, and SO₂, respectively. Findings suggest some seasonality, particularly for SO₂, with higher concentrations during colder months relative to warmer months, although a longer time frame of data is needed to evaluate seasonality fully. Correlation coefficients generally declined with distance between monitors, while coefficients of divergence increased with distance. However, these trends were not statistically significant. PM₁₀levels exceeded Chinese and other health-based standards and guidelines. The review identified 13 studies on outdoor air pollution and health. Although limited, the studies indicate that air pollution is associated with increased risk of health outcomes in Lanzhou. These studies and the high air pollution levels suggest potentially serious health consequences. Findings can provide guidance to future epidemiological studies, monitor placement programs, and air quality policies.

The extracellular polymeric substance (EPS) extracted from waste-activated sludge after short-time aerobic digestion was investigated to be used as a novel biosorbent for Cd²⁺removal from water. The sorption kinetics was well fit for the pseudo-second-order model, and the maximum sorption capacity of the EPS (430.3 mg Cd²⁺/g EPS) was markedly higher than those of the reported biosorbents. Both Langmuir model and Freundlich model commendably described the sorption isotherm. The Gibbs free energy analysis of the adsorption showed that the sorption process was feasible and spontaneous. According to the results of multiple analytical techniques, the adsorption process took place via both physical and chemical sorption, but the electrostatic interaction between sorption sites with the functional groups and Cd²⁺was the major mechanism.

Major ion chemistry (2000–2009) from 208 lakes (342 sample dates and 600 samples) in class I and II wilderness areas of the Sierra Nevada was used in the Steady-State Water Chemistry (SSWC) model to estimate critical loads for acid deposition and investigate the current vulnerability of high elevation lakes to acid deposition. The majority of the lakes were dilute (mean specific conductance = 8.0 μS cm⁻¹) and characterized by low acid neutralizing capacity (ANC; mean = 56.8 μeq L⁻¹). Two variants of the SSWC model were employed: (1) one model used the F-factor and (2) the alternate model used empirical estimates of atmospheric deposition and mineral weathering rates. A comparison between the results from both model variants resulted in a nearly 1:1 slope and an R²value of 0.98, suggesting that the deposition and mineral weathering rates used were appropriate. Using an ANCₗᵢₘᵢₜof 10 μeq L⁻¹, both models predicted a median critical load value of 149 eq ha⁻¹ year⁻¹of H⁺for granitic catchments. Median exceedances for the empirical approach and F-factor approach were −81 and −77 eq ha⁻¹ year⁻¹, respectively. Based on the F-factor and empirical models, 36 (17 %) and 34 (16 %) lakes exceeded their critical loads for acid deposition. Our analyses suggest that high elevation lakes in the Sierra Nevada have not fully recovered from the effects of acid deposition despite substantial improvement in air quality since the 1970s.

Anthropogenic CO₂ emission is identified as the major cause of climate change. The use of fossil fuels has to be accommodated, possibly with a CO₂ capture process. Sequestration of captured CO₂ at high pressure is proposed as a feasible option for future mitigation of climate change, though using fossil fuels. However, this needs significant energy input and carries the potential threat of a possible future catastrophe. Capture of CO₂ with possible recycling is a long-term sustainable option. In this paper, a process involving a chain of reactions using solid sodium to capture both CO₂ and SO₂ from a flue gas is described. A significantly detailed description of both chemical reactions and physical processes is discussed. Recycling of captured CO₂ and SO₂ in the form of solid graphite and elemental sulphur (as the by-products) is the special feature of this process. However, critical selection of intermediate process liquids and equipment in this process needs further study for real-life implementation of this scheme.

In this study, the magnetic cellulose nanomaterials, containing magnetic nanoscale zerovalent iron (nZVI) and cellulose, were prepared by a novel reduction method and characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and vibrating sample magnetometry (VSM). The XRD and XPS results demonstrated the formation of zerovalent iron nanoparticles in the nanocomposite materials. With a saturation magnetization of 57.2 emu g⁻¹, the cellulose@nZVI composites could be easily separated from solutions in 30 s through the external magnetic field. We investigated the adsorption performance of the magnetic cellulose nanomaterials for As(III) removal from aqueous solutions. The experimental results showed that arsenite adsorption followed the pseudo-second-order kinetic model and Langmuir isotherm model. A maximum removal of 99.27 % was observed for an initial concentration 10 mg L⁻¹, at pH 8.0, and an adsorbent dose of 1.0 g L⁻¹. Considering the high adsorption capacity, fast adsorption rate, and quick magnetic separation from treated water, the cellulose@nZVI composites were expected to be an efficient magnetic adsorbent for arsenic removal from aqueous solutions.

Lake Eğirdir is one of the most important freshwater resources in Turkey. The lake is located at the border of Isparta province in South West Turkey, an area known as the “Lakes District”. Lake Eğirdir is very important to the regional economy, but knowledge of its water quality is somewhat limited. Our objective was to assess the current water quality in Lake Eğirdir and its major tributaries, in order to provide information for future management decisions. The temperature, pH, electrical conductivity (EC), dissolved oxygen (DO) concentration, chemical oxygen demand (COD), nitrogen species concentrations, phosphorus species concentrations, and Chl-a concentrations were monitored monthly at seven sampling points in the lake between December 2010 and November 2011. The total nitrogen (TN) and total phosphorus (TP) loads were determined in the three main tributaries of Lake Eğirdir over the same period. At the end of the water quality assessment period, we determined that the lake water has the characteristics of class 1 waters for nitrogen species and class 2 waters for TP, according to the Turkish surface water quality management regulations. The Chl-a values measured in the lake were lower than expected from the trophic state index (TSI) values because of macrophyte growth in the lake. Interestingly, the total nitrogen/total phosphorus (TN/TP) ratios in the lake were low, possibly indicating that the sediment is a significant internal phosphorus resource in Lake Eğirdir.