In this research, the capability of vermiculite in arsenic extraction, associated with characterizing its main properties was evaluated. To address this purpose, vermiculite was artificially contaminated with arsenic at 7 and 28-day intervals. Then, arsenic was extracted from contaminated soils by different extractants. Various physical and mechanical tests were performed to investigate the effect of arsenic as an anionic contaminant on the properties of the vermiculite, as well as to evaluate how the properties of the contaminated soil were altered by the extraction process. The carbonate bonding phase was probably mainly responsible for the adsorption and fixation of arsenic with more than 50% portion among measured fractions at different curing times. Based on the vermiculite condition, hydrochloric acid was the best extractant for removing arsenic in all studied samples (around 3 -18 % more than other extractants). The clay soil demonstrated few changes due to arsenic contamination and modification. In general, the most promising characteristics of vermiculite as clay liner are its stability after contamination due to high CEC and SSA; however, its workability and strength (UCS between 110 to 220 kPa at different soil conditions) is a challenge and must be improved by adding coarser fractions like silt particles. In general, the results of this study regarding the effects of arsenic contamination and extraction onto vermiculite’s physical properties can provide appropriate information for researchers and geo-environmental engineers.

Algal biorefinery process utilizes every component of algal biomass to produce multiple useful fuel products. In this technique, acid pretreatment of algal biomass hydrolyzes microalgal carbohydrates into fermentable sugars, makes lipids more extractable and a protein part accessible for additional products. In the present study, Chlorella sorkiniana produced higher quantity of biodiesel than Botryococcus braunii and biomass in Botryococcus braunii was higher than the Chlorella sorkiniana. Botryococcus braunii produces 11% more lipid content than Chlorella sorkiniana which was consistent with biomass content. The total sugar (oligomeric and monomeric) yield attained by Combined Algal Processing (CAP) was 89.9%. 29 g/L ethanol was produced during the fermentation in the Pretreated Algal Slurry. The recovery of lipids from CAP was reported as 84–89% after fermentation and ethanol removal. CAP preserves the PUFA (Poly-Unsaturated Fatty Acids) and utilizes these high-value PUFAs to further reduce the cost of biofuel production and replace petroleum products.

Presence of microorganisms in soils strongly affects mobility of metals. This fact is often excluded when mobile metal fraction in soil is studied using extraction procedures. Thus, the first objective of this paper was to evaluate strain Aspergillus niger’s exometabolites contribution on aluminium mobilization. Fungal exudates collected in various time intervals during cultivation were analyzed and used for two-step bio-assisted extraction of alumina and gibbsite. Oxalic, citric and gluconic acids were identified in collected culture media with concentrations up to 68.4, 2.0 and 16.5 mmol L−1, respectively. These exometabolites proved to be the most efficient agents in mobile aluminium fraction extraction with aluminium extraction efficiency reaching almost 2.2%. However, fungal cultivation is time demanding process. Therefore, the second objective was to simplify acquisition of equally efficient extracting agent by chemically mimicking composition of main organic acid components of fungal exudates. This was successfully achieved with organic acids mixture prepared according to medium composition collected on the 12th day of Aspergillus niger cultivation. This mixture extracted similar amounts of aluminium from alumina compared to culture medium. The aluminium extraction efficiency from gibbsite by organic acids mixture was lesser than 0.09% which is most likely because of more rigid mineral structure of gibbsite compared to alumina. The prepared organic acid mixture was then successfully applied for aluminium extraction from soil samples and compared to standard single step extraction techniques. This showed there is at least 2.9 times higher content of mobile aluminium fraction in soils than it was previously considered, if contribution of microbial metabolites is considered in extraction procedures. Thus, our contribution highlights the significance of fungal metabolites in aluminium extraction from environmental samples, but it also simplifies the extraction procedure inspired by bio-assisted extraction of aluminium by common soil fungus A. niger.

Experimental investigations were carried out on removal of arsenic from contaminated groundwater by employing a new flat-sheet cross flow membrane module fitted with a hydrophobic polyvinylidenefluoride (PVDF) microfiltration membrane. The new design of the solar-driven membrane module in direct contact membrane distillation (DCMD) configuration successfully produced almost 100 per cent arsenic-free water from contaminated groundwater in a largely fouling-free operation while permitting high fluxes under reduced temperature polarization. For a feed flow rate of 0.120 m3/h, the 0.13 μm PVDF membrane yielded a high flux of 74 kg/(m2 h) at a feed water temperature of 40 °C and, 95 kg/m2 h at a feed water temperature of 60 °C. The encouraging results show that the design could be effectively exploited in the vast arsenic-affected rural areas of South-East Asian countries blessed with abundant sunlight particularly during the critical dry season. Solar-driven membrane distillation has the potential of removing arsenic from contaminated groundwater.

Between March 2006 and June 2008 removal of 34 trace elements was measured on a monthly basis at three horizontal-flow constructed wetlands in the Czech Republic designed to treat municipal wastewater. In general, the results indicated a very wide range of removal efficiencies among studied elements. The highest degree of removal (average of 90%) was found for aluminum. High average removal was also recorded for zinc (78%). Elements removed in the range of 50-75% were uranium, antimony, copper, lead, molybdenum, chromium, barium, iron and gallium. Removal of cadmium, tin, mercury, silver, selenium and nickel varied between 25 and 50%. Low retention (0-25%) was observed for vanadium, lithium, boron, cobalt and strontium. There were two elements (manganese and arsenic) for which average outflow concentrations were higher compared to inflow concentrations. Reduced manganese compounds are very soluble and therefore they are washed out under anaerobic conditions. The paper describes the removal of trace elements in constructed wetlands treating municipal sewage.

A molecularly imprinted polymer (MIP) for selective removal of 2,4-dichlorophenol (2,4-DCP) in water was prepared as microspheres by the reverse microemulsion polymerization method based on the non-covalent interactions between 2,4-DCP, oleic acid, and divinylbenzene in acetonitrile. Microspheres have been characterized by Fourier transform infrared spectrometer (FTIR) and energy dispersive X-ray spectrometer (EDS) studies with evidence of 2,4-DCP linkage in polymer particles and scanning electron microscopy (SEM) to study their morphological properties. The proper adsorption and selective recognition ability of the MIP were studied by an equilibrium-adsorption method. The MIP showed outstanding affinity towards 2,4-DCP in aqueous solution and the optimum pH value for binding has been found around the neutral range. The molecular recognition of 2,4-DCP was analyzed in detail by using molecular modeling software. In addition, by investigating the variation in the adsorption ability of the MIP, it clearly showed excellent reproducibility. Molecular imprinting has potential as a remediation technology in water treatment.

The evaluation of microbial availability of contaminants is of high importance for better reflecting the processes governing contaminant fate in soil and for establishing the risk associated with contaminated sites. A sub-critical water extraction technique was assessed for its potential to determine the microbially degradable fraction of [14C]phenanthrene-associated activity in two dissimilar soils at three different ageing times (14, 28 and 49 days). For the majority of determinations, no significant (p > 0.05) difference between sub-critical water-extracted 14C-activity at 160 °C and the fraction mineralized by catabolically active Pseudomonas sp. was observed. Collectively, the results suggested that the sub-critical water extraction technique was an appropriate technique for predicting the biodegradable fraction of phenanthrene-associated 14C-activity in dissimilar soils following increasing soil-contaminant contact time. Sub-critical water extraction reflects phenanthrene bioaccessibility in the soil.