Fuzzy rule-based modelling for human health risk from naturally occurring radioactive materials in produced water

Produced water, discharged from offshore oil and gas operations, contains chemicals from formation water, condensed water, and any chemical added down hole or during the oil/water separation process. Although, most of the contaminants fall below the detection limits within a short distance from the discharge port, a few of the remaining contaminants including naturally occurring radioactive materials (NORM) are of concern due to their bioavailability in the media and bioaccumulation characteristics in finfish and shellfish species used for human consumption. In the past, several initiatives have been taken to model human health risk from NORM in produced water. The parameters of the available risk assessment models are imprecise and sparse in nature. In this study, a fuzzy possibilistic evaluation using fuzzy rule based modeling has been presented. Being conservative in nature, the possibilistic approach considers possible input parameter values; thus provides better environmental prediction than the Monte Carlo (MC) calculation. The uncertainties of the input parameters were captured with fuzzy triangular membership functions (TFNs). Fuzzy if-then rules were applied for input concentrations of two isotopes of radium, namely (226)Ra, and (228)Ra, available in produced water and bulk dilution to evaluate the radium concentration in fish tissue used for human consumption. The bulk dilution was predicted using four input parameters: produced water discharge rate, ambient seawater velocity, depth of discharge port and density gradient. The evaluated cancer risk shows compliance with the regulatory guidelines; thus minimum risk to human health is expected from NORM components in produced water.     

Recycling of nickel smelter slag for arsenic remediation—an experimental study

In this study, recycled Ni smelter slag has been used as a reactive medium for arsenic (As) removal from aqueous solutions. The results of the study showed that 10.16–11.43-cm long columns containing 451–550 g of slag operated for at least 65 days were able to remove 99–100 % As species from continuously flowing contaminated water at an initial As concentration of 10 mg/L. The removal capacities were found to be 1.039 to 1.054 mg As per g of slag. X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy data also showed that electrostatic attraction and oxidation–reduction reactions between As species and mixed iron oxides present in the slag were the main mechanisms for the removal of arsenic from aqueous solutions. Theoretical multiplet analysis of XPS data revealed that the amount of goethite in the slag increased from 22 to 60 % during arsenic removal by adsorption and the percentage of magnetite decreased from 50 to 40 %. These changes indicate that redox-mediated reactions occurred as part of the As(V) removal process. Raman spectroscopy studies confirmed that, in addition to surface reactions, internal interactions between the slag and arsenic also occurred. The findings of the study suggest that recycled Ni smelter slag could be an effective low-cost reactive medium for a subsurface remediation system, such as a permeable reactive barrier. Recycling of waste material (slag) for the removal of another waste (arsenic) can significantly reduce the environmental footprint of metallurgical operations and hence contribute to sustainable development. Such recycling also decreases slag disposal costs and eliminates the need to purchase commercial reactive material or obtain expensive natural material for remediation purposes.     

Complete degradation of di-n-octyl phthalate by Gordonia sp. strain Dop5

The present study describes the assimilation of di-n-octyl phthalate by an aerobic bacterium, isolated from municipal waste-contaminated soil sample utilizing di-n-octyl phthalate as the sole source of carbon and energy. The isolate was identified as Gordonia sp. based on the morphological, nutritional and biochemical characteristics as well as 16S rRNA gene sequence analysis. A combination of chromatographic and spectrometric analyses revealed a complete di-n-octyl assimilation pathway. In the degradation process, mono-n-octyl phthalate, phthalic acid, protocatechuic acid and 1-octanol were identified as the degradation products of di-n-octyl phthalate. Furthermore, phthalic acid was metabolized via protocatechuic acid involving protocatechuate 3,4-dioxygenase while 1-octanol was metabolized by NAD⁺-dependent dehydrogenases to 1-octanoic acid, which was subsequently degraded via β-oxidation, ultimately, leading to tricarboxylic acid cycle intermediates. Apart from phthalic acid and 1-octanol metabolizing pathway enzymes, two esterases, di-n-octyl phthalate hydrolase and mono-n-octyl phthalate hydrolase involved in di-n-octyl phthalate degradation were found to be inducible in nature. This is the first report on the metabolic pathway involved in the complete degradation of di-n-octyl phthalate by a single bacterial isolate, which is also capable of efficiently degrading other phthalate esters of environmental concern having either shorter or longer alkyl chains.     

Underwater treatment of lead-contaminated sediment

The sediment associated with the reconstruction of a bridge pier was classifiable as hazardous by the Toxicity Characteristic Leaching Procedure (TCLP), due to elevated concentrations of lead. However, RCRA regulations do not classify the sediment as hazardous unless it is moved. RMT designed an in-situ, underwater treatment process to render the sediment nonhazardous, using phosphate-based chemistry before dredging. Subsequent sediment management was conducted without the additional regulatory requirements and costs associated with managing hazardous waste.     

COMPARING SOME METHODS OF ESTIMATING MEAN AREAL RAINFALL1

ABSTRACT: A comparison of 13 different methods of estimating mean areal rainfall was made on two areas in New Mexico, U.S.A., and one area in Great Britain. Daily, monthly and yearly rainfall data were utilized. All methods, in general, yielded comparable estimates, especially for yearly values. This suggested that a simpler method would be preferable for estimating mean areal rainfall in these areas.     

Comparative studies on biomass productivity and lipid content of a novel blue-green algae during autotrophic and heterotrophic growth

Environmental Science and Pollution Research - Algae have long been acclaimed as the attractive renewable source for generating third-generation biofuels, particularly biodiesel. Under the present...     

Co-composting solid biowastes with alkaline materials to enhance carbon stabilization and revegetation potential

Co-composting biowastes such as manures and biosolids can be used to stabilize carbon (C) without impacting the quality of these biowastes. This study investigated the effect of co-composting biowastes with alkaline materials on C stabilization and monitored the fertilization and revegetation values of these co-composts. The stabilization of C in biowastes (poultry manure and biosolids) was examined by their composting in the presence of various alkaline amendments (lime, fluidized bed boiler ash, flue gas desulphurization gypsum, and red mud) for 6 months in a controlled environment. The effects of co-composting on the biowastes’ properties were assessed for different physical C fractions, microbial biomass C, priming effect, potentially mineralizable nitrogen, bioavailable phosphorus, and revegetation of an urban landfill soil. Co-composting biowastes with alkaline materials increased C stabilization, attributed to interaction with alkaline materials, thereby protecting it from microbial decomposition. The co-composted biowastes also increased the fertility of the landfill soil, thereby enhancing its revegetation potential. Stabilization of biowastes using alkaline materials through co-composting maintains their fertilization value in terms of improving plant growth. The co-composted biowastes also contribute to long-term soil C sequestration and reduction of bioavailability of heavy metals.     

Using adsorption and sulphide precipitation as the principal removal mechanisms of arsenic from a constructed wetland – a critical review

This review has been undertaken to understand the role of various parameters such as redox potential, microbes, and organic matters on the fate and transport of arsenic in the constructed wetland. A conceptual diagram of arsenic fate and transport in the constructed wetland was developed. Role of various minerals which are produced due to microbial activities are described. The role of these minerals on arsenic adsorption is discussed. It was envisaged that iron sulphide would be the main adsorbent for arsenic in microbe-mediated adsorption process. Beside microbe-mediated arsenic adsorption, roles of various microbes, such as sulphate reducers and methane producers, on arsenic transformation are discussed. Role of various organic carbon sources and electron acceptors on the proliferation of the above mentioned microbes with respect to arsenic transformation was envisaged. Role of dissolved organic matters on arsenic transformation and transport was also discussed in details. To strengthen the review, laboratory studies and modelling of arsenic adsorption and transformation using the Visual Minteq were appended.     

Concentrations of some heavy metals in commercially important finfish and shellfish of the River Ganga

Heavy metals are dangerous to aquatic organisms and it can be bioaccumulated in the food chain leading to diseases in human. Cumulative effects of metals or chronic poisoning may occur as a result of long-term exposure even to low concentrations. The accumulation of heavy metals varies depending upon the species, environmental conditions, and inhibitory processes. Concentrations of zinc, copper, lead, and cadmium were determined in finfish and shellfish species in the Gangetic delta using a PerkinElmer Sciex ELAN 5000 ICP mass spectrometer and expressed as milligrams per kilogram of dry weight. In finfish and shellfish species the concentrations of Zn, Cu, Pb, and Cd were comparatively higher at stations 1 and 2 than the permissible level of WHO. The concentration of metals exhibited significant spatial variation and followed the order station 1 > station 2 > station 3 > station 4, which may be related to different degree of contamination in different location. The metal accumulation exhibited species specificity.