Removal of arsenate from water by adsorbents: a comparative case study

Laboratory and field filtration experiments were conducted to study the effectiveness of As(V) removal for five types of adsorbent media. The media included activated alumina (AA), modified activated alumina (MAA), granular ferric hydroxide (GFH), granular ferric oxide (GFO), and granular titanium dioxide (TiO?). In laboratory batch and column experiments, the synthetic challenge water was used to evaluate the effectiveness for five adsorbents. The results of the batch experiments showed that the As(V) adsorption decreased as follows at pH 6.5: TiO? > GFO > GFH > MAA > AA. At pH 8.5, however, As(V) removal decreased in the following order: GFO = TiO? > GFH > MAA > AA. In column experiments, at pH 6.5, the adsorbed As(V) for adsorbents followed the order: TiO? > GFO > GFH, whereas at pH 8.5 the order became: GFO = TiO? > GFH when the challenge water containing 50 μg/L of As(V) was used. Field filtration experiments were carried out in parallel at a wellhead in New Jersey. Before the effluent arsenic concentration increased to 10 μg/L, approximately 58,000 and 41,500 bed volumes of groundwater containing an average of 47 μg/L of As(V) were treated by the filter system packed with GFO and TiO?, respectively. The As(V) adsorption decreased in the following sequence: GFO > TiO? > GFH > MAA > AA. Filtration results demonstrated that GFO and TiO? adsorbents could be used as media in small community filtration systems for As(V) removal.     

Lichens reveal air PAH fractionation in the Himalaya

This paper shows that gas/particulate phase partitioning of polycyclic aromatic hydrocarbons (PAHs) can be monitored using lichens. Anthropogenic sources are responsible for the release of PAHs, which are bioaccumulated in plants at various spatial scales based on their physicochemical properties. Atmospheric PAHs are distributed both in the gaseous and particulate states. Here, a lichen species, Dermatocarpon vellereum Zschacke, has been collected at different altitudes in and around the Rudraprayag valley, located in Central Himalayan region of India, in order to study the spatial distribution of PAHs in the valley. Results show that PAH concentration ranged from 0.136 to 4.96 μg g^?1. Findings reveal that the bioaccumulation of 2- and 3-ringed PAHs was higher in high-altitude samples, whereas bioaccumulation of fluoranthene, a 4-ringed PAH, showed higher concentration in samples from localities away from town centre. 5- and 6-ring PAHs were then confined to the lower altitude at the base of the valley, thus justifying their particulate-bound nature. This is the first report showing the utility of lichen to biomonitor PAHs in the Himalayan ecosystem.     

Characterization and modeling of nutrient-deficient tomato-processing wastewater treatment using an anaerobic/aerobic system

Tomato-processing wastewaters are typical of slowly biodegradable high strength wastewaters generated from the food canning industry. Three different samples of influent and three samples of anaerobic effluents corresponding to the three influents collected from an on-site pilot-scale anaerobic/aerobic system were characterized using respirometric methods. Respirometric studies demonstrated that the pretreatment in the anaerobic reactor of the pilot-scale system increased the readily biodegradable fraction from an average of 40% of the SCOD in the influent to 50% of the SCOD in the anaerobic effluent, improved kinetics from an average micro(max) of 1.5d(-1) in the influent to 3.5d(-1) in the anaerobic effluent, and eliminated nutrient deficiency. Furthermore, the system was calibrated and simulated by application of wastewater characterization and biokinetic data derived form respirometric tests of influent and anaerobic effluent in Activated Sludge Model no.1 (ASM1).     

Removal of cyanotoxins from surface water resources using reusable molecularly imprinted polymer adsorbents

Introduction

Microcystins (MCs; cyclic heptapeptides) are produced by freshwater cyanobacteria and cause public health concern in potable water supplies. There are more than 60 types of MCs identified to date, of which MC-LR is the most common found worldwide. For MC-LR, the WHO has established a threshold value of 1???g?L^?1 for drinking water. The present MCs removal methods such as coagulation, flocculation, adsorption, and filtration showed low efficiency for removing dissolved MC fraction from surface waters to the stipulated limit prescribed by WHO based on MC health impacts. The search for cost-effective and efficient removal method is still warranted for remediation of dissolved MC-LR-contaminated water resources.

Materials and methods

Molecularly imprinted polymer (MIP) adsorbent has been prepared using non-covalent imprinting approach. Using MC-LR as a template, itaconic acid as a functional monomer, and ethylene glycol dimethacrylate as a cross-linking monomer, a MIP has been synthesized. Computer simulations were used to design effective binding sites for MC-LR binding in aqueous solutions. Batch binding adsorption assay was followed to determine binding capacity of MIP under the influence of environmental parameters such as total dissolved solids and pH.

Results and discussion

The adsorptive removal of MC-LR from lake water has been investigated using MIPs. The MIP showed excellent adsorption potential toward MC-LR in aqueous solutions with a binding capacity of 3.64???g?mg^?1 which is about 60% and 70% more than the commercially used powdered activated carbon (PAC) and resin XAD, respectively. Environmental parameters such as total organic carbon (represented as chemical oxygen demand (COD)) and total dissolved solids (TDS) showed no significant interference up to 300?mg?L^?1 for MC-LR removal from lake water samples. It was found that the binding sites on PAC and XAD have more affinity toward COD and TDS than the MC-LR. Further, the adsorption capacity of the MIP was evaluated rigorously by its repeated contact with fresh lake water, and it was found that the adsorption capacity of the MIP did not change even after seven adsorption/desorption cycles. The contaminated water of MC-LR (1.0???g?L^?1) of 3,640?L could be treated by 1?g of MIP with an estimated cost of US $1.5.

Conclusions

The adsorption capacity of the MIP is 40% more than commercially used PAC and resins and also the polymer showed reusable potential which is one of the important criteria in selection of cyanotoxins remediation methods.     

Protein futures for Western Europe: potential land use and climate impacts in 2050

Multiple production and demand side measures are needed to improve food system sustainability. This study quantified the theoretical minimum agricultural land requirements to supply Western Europe with food in 2050 from its own land base, together with GHG emissions arising. Assuming that crop yield gaps in agriculture are closed, livestock production efficiencies increased and waste at all stages reduced, a range of food consumption scenarios were modelled each based on different ‘protein futures’. The scenarios were as follows: intensive and efficient livestock production using today’s species mix; intensive efficient poultry–dairy production; intensive efficient aquaculture–dairy; artificial meat and dairy; livestock on ‘ecological leftovers’ (livestock reared only on land unsuited to cropping, agricultural residues and food waste, with consumption capped at that level of availability); and a ‘plant-based eating’ scenario. For each scenario, ‘projected diet’ and ‘healthy diet’ variants were modelled. Finally, we quantified the theoretical maximum carbon sequestration potential from afforestation of spared agricultural land. Results indicate that land use could be cut by 14–86 % and GHG emissions reduced by up to approximately 90 %. The yearly carbon storage potential arising from spared agricultural land ranged from 90 to 700 Mt CO₂ in 2050. The artificial meat and plant-based scenarios achieved the greatest land use and GHG reductions and the greatest carbon sequestration potential. The ‘ecological leftover’ scenario required the least cropland as compared with the other meat-containing scenarios, but all available pasture was used, and GHG emissions were higher if meat consumption was not capped at healthy levels.     

Distribution Of Cadmium And Nickel Among Various Forms In Natural And Contaminated Soils Amended With Edta

Because of its strong chelating capacity, application of ethylenediaminetetraacetic acid (EDTA) to soils may change the amount and distribution of heavy metals among their various chemical forms. Therefore, a greenhouse experiment was conducted using two cultivars of Brassica species (Brassica juncea and Brassica carinata) as hyper accumulator test crops on natural and artificially Cd and Ni contaminated soils. Both natural and metal amended soils were treated with disodium salt of EDTA at 0 and 1 g kg^–1 soil. After harvest of crops, soil samples were fractionated into water soluble plus exchangeable (WE), carbonate (CARB), organic matter (OM), Mn oxide (MnOX), amorphous Fe oxide (AFeOX), crystalline Fe oxide (CFeOX) and residual (RES) fractions. In metal amended soils, Cd and Ni were found predominantly in the AFeOX fraction in the absence of EDTA application and in the WE fraction in EDTA treated soil. Application of EDTA resulted in the redistribution of Cd among different forms and increased significantly Cd in the WE fraction with a concomitant significant decrease in the OM fraction. In natural soils, more than 40% of the total Cd was present in the RES fraction while in contaminated soil it was only 5%. Nickel in the WE fraction increased significantly while it considerably decreased in the CARB, OM, MnOX, AFeOX and CFeOX fractions with EDTA addition. This indicated that applied EDTA is capable to move Cd and Ni from the less soluble or more stable forms (CARB, OM, MnOX, AFeOX and CFeOX) to the most soluble form (WE). N natural soils, Ni in the RES fraction was found upto 49%, whereas only 10% of the total Ni was observed in contaminated soil, irrespective of EDTA treatment. In general, the amount of Cd recovered after harvest of both the Brassica cultivars did not differ significantly in any fraction except the WE fraction. The amount of Ni recovered in the AFeOX fraction was significantly higher after harvest of B. juncea as compared to B. carinata.Readers should send their comments on this paper to: BhaskarNath@aol.com within 3 months of publication of this issue.