PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Waste Management”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,747 records · Page 97Linked to original sources

Characterization of red mud derived from a combined Bayer Process and bauxite calcination method.

Red mud can be derived from the processing of bauxite using different methods. The chemical and mineralogical composition of the combined Bayer Process and bauxite calcination red mud (BPBCRM) differs markedly from those of the pure Bayer Process red mud (PBPRM). In this study, red mud derived from a combined Bayer Process and bauxite calcination method was characterized. The results show that pH of the red mud decreased with increasing duration of storage time. Na dominated among the soluble cations, but the concentration of soluble Na decreased with increasing duration of storage time as a result of leaching. Cation exchange capacity also decreased with increasing duration of storage time, probably due to a decrease in pH causing a reduction in negatively charged sites on the red mud particles. Ca was the predominant exchangeable cation in the fresh red mud but the concentration of exchangeable Ca markedly decreased in the old red mud, which was dominated by exchangeable Na. The degree of crystallization and thermal stability of the red mud increased with increasing duration of storage. The acid neutralizing capacity of red mud obtained from this study was about 10 mol kg(-1), which is much greater than the reported values for the pure Bayer Process red mud. Column filtering experiment indicates that the red mud also had a very strong capacity to remove Cu, Zn and Cd from the filtering solution. It is conservatively estimated that the simultaneous removal rates of Cd, Zn and Cu by red mud are over 22,250 mg kg(-1), 22,500 mg kg(-1) and 25,000 mg kg(-1), respectively. The affinity of these metals to the red mud was in the following decreasing order: Cu>Zn>Cd. In general, the fresh red mud retained more heavy metals than the old red mud did.

Aluminum Oxide↗

Gliding arc plasma processing of CO2 conversion.

Conversion of carbon dioxide (CO2) using gliding arc plasma was performed. The research was done to investigate the effect of variation of total gas flow rates and addition of auxiliary gases--N2, O2, air, water--to the CO2 conversion process. This system shows higher power efficiency than other nonthermal plasma methods. Experiment results indicate the conversion of CO2 reaches 18% at total gas flow rate of 0.8 L/min and produces CO and O2 as the main gaseous products. Among auxiliary gases, only N2 gives positive effect on CO2 conversion and the power efficiency at N2 concentration of 95% and total gas flow rate of 2 L/min increases about three times compared to pure CO2 process.

Air Pollutants↗

The EU Directive on port reception facilities for ship-generated waste and cargo residues: the results of a second survey on the provision and uptake of facilities in North Sea ports.

The aim of this paper is to evaluate the results of a survey of the availability and uptake of port reception facilities within the North Sea area. The evaluation is based primarily on original survey data from the autumn of 2002 which followed on from a similar survey conducted in the summer of 2000. The EU Directive on port reception facilities for ship-generated waste etc. (Directive 2000/59/EC) was due to enter into force in December 2002, and required all EU ports to provide reception facilities to meet the needs of the vessels normally calling in at them. This paper examines the readiness of North Sea ports to meet that requirement and also considers the actual uptake levels of facilities, where ports were able to provide such information.

Commerce↗

Removal of organic contaminants by RO and NF membranes.

Rejection characteristics of organic and inorganic compounds were examined for six reverse osmosis (RO) membranes and two nanofiltration (NF) membranes that are commercially available. A batch stirred-cell was employed to determine the membrane flux and the solute rejection for solutions at various concentrations and different pH conditions. The results show that for ionic solutes the degree of separation is influenced mainly by electrostatic exclusion, while for organic solutes the removal depends mainly upon the solute radius and molecular structure. In order to provide a better understanding of rejection mechanisms for the RO and NF membranes, the ratio of solute radius (r(i,s)) to effective membrane pore radius (r(p)) was employed to compare rejections. An empirical relation for the dependence of the rejection of organic compounds on the ratio r(i,s)/r(p) is presented. The rejection for organic compounds is over 75% when r(i,s)/r(p) is greater than 0.8. In addition, the rejection of organic compounds is examined using the extended Nernst-Planck equation coupled with a steric hindrance model. The transport of organic solutes is controlled mainly by diffusion for the compounds that have a high r(i,s)/r(p) ratio, while convection is dominant for compounds that have a small r(i,s)/r(p) ratio.

2-Propanol↗

The changing view of acrylamide neurotoxicity.

Acrylamide (ACR) is a water-soluble, vinyl monomer that has multiple chemical and industrial applications: e.g., waste water management, ore processing. In addition, ACR is used extensively in molecular laboratories for gel chromatography and is present in certain foods that have been prepared at very high temperatures. Extensive studies in rodents and other laboratory animals have provided evidence that exposure to monomeric ACR causes cellular damage in both the nervous and reproductive systems, and produces tumors in certain hormonally responsive tissues. Whereas human epidemiological studies have demonstrated a significantly elevated incidence of neurotoxicity in occupationally exposed populations, such research has not, to date, revealed a corresponding increase in cancer risk. Since the announcement by a Swedish research group in April 2002 [J. Ag. Food Chem. 50 (2002) 4998] regarding the presence of ACR in potato and grain-based foods, there has been a renewed interest in the toxic actions of this chemical. Therefore, in this review, we consider the different toxic effects of ACR. The neurotoxic actions of ACR will be the focal point since neurotoxicity is a consequence of both human and laboratory animal exposure and since this area of investigation has received considerable attention over the past 30 years. As will be discussed, a growing body of evidence now indicates that the nerve terminal is a primary site of ACR action and that inhibition of corresponding membrane-fusion processes impairs neurotransmitter release and promotes eventual degeneration. The electrophilic nature of ACR suggests that this neurotoxicant adducts nucleophilic sulfhydryl groups on certain proteins that are critically involved in membrane fusion. Adduction of thiol groups also might be common to the reproductive and carcinogenic effects of ACR. A final goal of this review is to identify data gaps that retard a comprehensive understanding of ACR pathophysiological processes.

Acrylamide↗

Developments in ultrasound--non-medical.

Ultrasound is defined as sound of a frequency that is too high for the human ear to detect--i.e. it is inaudible. Nevertheless this "silent sound" has a large range of applications in science, medicine and industry. The study of the effects of ultrasound on materials--known as sonochemistry--is one of the broadest and most exciting areas in current research. In this review some recent developments with major potential are identified from the fields environmental protection and materials processing. Environmental protection can refer to methods of preventing pollution or to the removal of existing pollution. Here we will look at examples drawn from the latter in which ultrasound has been used for the purification of water (chemical and biological), the decontamination of the atmosphere and soil remediation i.e. the classic three domains of water, air and land. In terms of materials processing two examples have been chosen, the treatment of sewage sludge and the control of crystallisation. In both of these cases it is predominantly the mechanical effects of acoustic cavitation, which produce the enhanced digestion, and dewatering of sludge and provide for the control in crystallisation processes.

Bioreactors↗

Degradation of pentachlorophenol in cyclodextrin extraction effluent using a photocatalytic process.

This work evaluates a process for the elimination of pentachlorophenol (PCP) from effluents provided by a cyclodextrin-assisted flushing of contaminated soils. The effectiveness of photocatalytic degradation of PCP in several cyclodextrin (CD) solutions was evaluated using TiO2 as a photocatalyst. Effects of CD type on PCP degradation rate were studied at two pH values. A similar effect was observed for all CDs used on degradation rate of PCP and the decay of PCP was found to be less extensive at pH 11 than at pH 7. The kinetic orders of the photocatalytic reactions of PCP for all of the solutions have been determined. The first-order rate constants were found to be 0.0884, 0.0362, 0.0197 and 0.0053 min(-1) in CD solutions, respectively, at 0, 1, 2 and 5 mmol l(-1) of CD. Batch experiments were performed in order to study the CD extraction enhancement of PCP previously adsorbed on soil. The results show that the removal capacity of PCP from soil increases with CD concentration (from 0 to 5 mmol l(-1)). When the CD concentration was 5 mmol l(-1), an extraction of about 70% of PCP adsorbed on soil was observed, whereas only 37% was removed when water was used as the flushing solution. The optimal conditions for such a coupled method depend on the nature and concentration of the extracting agent and also on the photocatalytic experimental conditions. This work revealed that the coupling of cyclodextrin-enhanced solubilization and photocatalytic treatment is a promising method for contaminated soil remediation.

2-Hydroxypropyl-beta-cyclodextrin↗

Chemical behaviour of the Wheal Jane bioremediation system.

The effectiveness of remediation of the highly acidic and transition metal polluted mine water discharge from the Wheal Jane Mine by the Wheal Jane Passive Treatment Plant is described. The success of the remediation required that all the system components work as predicted. The study shows considerable success in the removal of key toxic metals and clearly demonstrates the potential for natural attenuation of acid mine drainage, particularly iron oxidation, by microbial populations. The Wheal Jane Passive Treatment Plant provides the only experimental facility of its kind.

Aerobiosis↗

Microbiology of a wetland ecosystem constructed to remediate mine drainage from a heavy metal mine.

A pilot passive treatment plant (PPTP) was constructed to evaluate the potential of a composite wetland system to remediate acidic, metal-rich water draining the former Wheal Jane tin, in Cornwall, England. The treatment plant consists of three separate and controllable composite systems, each of which comprises a series of aerobic wetlands for iron oxidation and precipitation, a compost bioreactor for removing chalcophilic metals and to generate alkalinity, and rock filter ponds for removing soluble manganese and organic carbon. To understand the roles of microorganisms in remediating acid mine drainage (AMD) in constructed wetland ecosystems, populations of different groups of cultivatable acidophilic microbes in the various components of the Wheal Jane PPTP were enumerated over a 30-month period. Initially, moderately acidophilic iron-oxidising bacteria (related to Halothiobacillus neapolitanus) were found to be the major cultivatable microorganisms present in the untreated AMD, though later heterotrophic acidophiles emerged as the dominant group, on a numerical basis. Culturable microbes in the surface waters and sediments of the aerobic wetlands were similarly dominated by heterotrophic acidophiles, though both moderately and extremely acidophilic iron-oxidising bacteria were also present in significant numbers. The dominant microbial isolate in waters draining the anaerobic compost bioreactors was an iron- and sulfur-oxidising moderate acidophile that was closely related to Thiomonas intermedia. The acidophiles enumerated at the Wheal Jane PPTP accounted for 1% to 25% of the total microbial population. Phylogenetic analysis of 14 isolates from various components of the Wheal Jane PPTP showed that, whilst many of these bacteria were commonly encountered acidophiles, some of these had not been previously encountered in AMD and AMD-impacted environments.

Bacteria↗

Biogeochemistry of the compost bioreactor components of a composite acid mine drainage passive remediation system.

The compost bioreactor ("anaerobic cell") components of three composite passive remediation systems constructed to treat acid mine drainage (AMD) at the former Wheal Jane tin mine, Cornwall, UK were studied over a period of 16 months. While there was some amelioration of the preprocessed AMD in each of the three compost bioreactors, as evidenced by pH increase and decrease in metal concentrations, only one of the cells showed effective removal of the two dominant heavy metals (iron and zinc) present. With two of the compost bioreactors, concentrations of soluble (ferrous) iron draining the cells were significantly greater than those entering the reactors, indicating that there was net mobilisation (by reductive dissolution) of colloidal and/or solid-phase ferric iron compounds within the cells. Soluble sulfide was also detected in waters draining all three compost bioreactors which was rapidly oxidised, in contrast to ferrous iron. Oxidation and hydrolysis of iron, together with sulfide oxidation, resulted in reacidification of processed AMD downstream of the compost bioreactors in two of the passive treatment systems. The dominant cultivatable microorganism in waters draining the compost bioreactors was identified, via analysis of its 16S rRNA gene, as a Thiomonas sp. and was capable of accelerating the dissimilatory oxidation of both ferrous iron and reduced sulfur compounds. Sulfate-reducing bacteria (SRB) were also detected, although only in the bioreactor that was performing well were these present in significant numbers. This particular compost bioreactor had been shut down for 10 months prior to the monitoring period due to operational problems. This unforeseen event appears to have allowed more successful development of AMD-tolerant and other microbial populations with critical roles in AMD bioremediation, including neutrophilic SRB (nSRB), in this compost bioreactor than in the other two, where the throughput of AMD was not interrupted. This study has revealed new insights into the operation of compost bioreactors used to remediate mine waters and has shown that, when operated under appropriate conditions, they can be highly efficient at generating alkalinity and removing metals from extremely acidic, metal-rich AMD.

Biochemistry↗

Characteristics and stabilities of residues from the Wheal Jane constructed wetlands.

The characteristics and solubilities of residues formed during effluent treatment at the Wheal Jane constructed wetland facility in Cornwall, UK are described. The constructed wetland treats an acidic (pH 3 to 4) mine discharge enriched in iron (<100 mg/l), zinc (<80 mg/l), manganese (<20 mg/l) and arsenic (<2 mg/l). The processing strategy adopted at the site is to remove elements selectively from the mine water in distinct unit process operations and concentrate the iron and base metals into residues within the circuits. Solubility tests conducted on the materials from the aerobic and anaerobic cells attempt to simulate future possible leaching processes within landfill sites used for ultimate disposal. The tests used in the evaluation included TCLP, MARG, washing and column leaching. The aerobic solids overall have very low solubilities which are well below the TCLP thresholds for As, Cd and Pb. The TCLP results for these toxic elements are supported by the washing and column test work. The anaerobic substrates are carbonaceous in nature, composed of straw, wood pulp and manure. They contain minimal amounts of toxic compounds and are considered to be less of a disposal problem. Ochre precipitated at a pH of 3-4 in the aerobic cells contains significant concentrations of arsenic (>0.1%). This element is carcinogenic, and such residues are classified as hazardous waste under current UK landfill regulations. This classification does not take into consideration the solubility of the material but is based solely on the bulk chemical composition.

Aerobiosis↗

Trends in biomass and metal sequestration associated with reeds and algae at Wheal Jane Biorem pilot passive treatment plant.

An assessment of the rate of biomass production both of the reeds in the aerobic cells and the algae in the rock filters, which form the final stage in the series of treatment cells, has been undertaken. The biomass production for the reeds was found to be highest for the lime-dosed anoxic limestone drain system, but even this was very low in comparison to values reported for natural and constructed wetlands. The algal coverage of each lagoon was relatively homogeneous, with no significant difference between the three systems studied. However, too many unknown factors suggest that further study is required. The metal uptake was higher in the roots than the stems, although no variation between cells of systems was detectable, and the difference was not as marked as reported by other workers. The metal concentrations in the debris samples were markedly higher than the roots of the reeds. The values for Fe, Al and As were several orders of magnitude larger than the influent minewater. Further study is required here, but this appears to be a key component in the function of the reeds. The lime-dosed system rock filter showed the highest Fe removal rate but the lowest Mn removal rate. Some possible mechanisms are discussed in the paper, but further investigation would be required to test these hypotheses.

Aerobiosis↗

Biological manganese removal from acid mine drainage in constructed wetlands and prototype bioreactors.

Mine drainage waters vary considerably in the range and concentration of heavy metals they contain. Besides iron, manganese is frequently present at elevated concentrations in waters draining both coal and metal mines. Passive treatment systems (aerobic wetlands and compost bioreactors) are designed to remove iron by biologically induced oxidation/precipitation. Manganese, however, is problematic as it does not readily form sulfidic minerals and requires elevated pH (>8) for abiotic oxidation of Mn (II) to insoluble Mn (IV). As a result, manganese removal in passive remediation systems is often less effective than removal of iron. This was found to be the case at the pilot passive treatment plant (PPTP) constructed to treat water draining the former Wheal Jane tin mine in Cornwall, UK, where effective removal of manganese occurred only in one of the three rock filter components of the composite systems over a 1-year period of monitoring. Water in the two rock filter systems where manganese removal was relatively poor was generally <pH 5, whereas it was significantly higher ( approximately pH 7) in the third (effective) system. These differences in water chemistry and manganese removal were due to variable performances in the compost bioreactors that feed the rock filter units in the composite passive systems at Wheal Jane. An alternative approach for removing soluble manganese from mine waters, using fixed bed bioreactors, was developed. Ferromanganese nodules (about 2 cm diameter), collected from an abandoned mine adit in north Wales, were used to inoculate the bioreactors (working volume ca. 700 ml). Following colonization by manganese-oxidizing microbes, the aerated bioreactor catalysed the removal of soluble manganese, via oxidation of Mn (II) and precipitation of the resultant Mn (IV) in the bioreactor, in synthetic media and mine water from the Wheal Jane PPTP. Such an approach has potential application for removing soluble Mn from mine streams and other Mn-contaminated water courses.

Bacteria↗

The Wheal Jane wetlands model for bioremediation of acid mine drainage.

Acid mine drainage (AMD) is a widespread environmental problem associated with both working and abandoned mining operations. As part of an overall strategy to determine a long-term treatment option for AMD, a pilot passive treatment plant was constructed in 1994 at Wheal Jane Mine in Cornwall, UK. The plant consists of three separate systems, each containing aerobic reed beds, anaerobic cell and rock filters, and represents the largest European experimental facility of its kind. The systems only differ by the type of pretreatment utilised to increase the pH of the influent minewater (pH <4): lime dosed (LD), anoxic limestone drain (ALD) and lime free (LF), which receives no form of pretreatment. Historical data (1994-1997) indicate median Fe reduction between 55% and 92%, sulphate removal in the range of 3-38% and removal of target metals (cadmium, copper and zinc) below detection limits, depending on pretreatment and flow rates through the system. A new model to simulate the processes and dynamics of the wetlands systems is described, as well as the application of the model to experimental data collected at the pilot plant. The model is process based, and utilises reaction kinetic approaches based on experimental microbial techniques rather than an equilibrium approach to metal precipitation. The model is dynamic and utilises numerical integration routines to solve a set of differential equations that describe the behaviour of 20 variables over the 17 pilot plant cells on a daily basis. The model outputs at each cell boundary are evaluated and compared with the measured data, and the model is demonstrated to provide a good representation of the complex behaviour of the wetland system for a wide range of variables.

Biochemistry↗

Metal transfer to plants grown on a dredged sediment: use of radioactive isotope 203Hg and titanium.

Improperly disposed of dredged sediments contaminated with metals may induce long-term leaching and an increase of metal concentrations in ground waters and vegetal cover plants. The objective of the study was to quantify the sediment-to-plant transfer of Cu, Pb, Hg and Zn with a particular focus on the pathway of Hg and to determine whether the establishment of vegetal cover modifies the metal availability. A pot experiment with rape (Brassica napus), cabbage (Brassica oleraccea) and red fescue (Festuca rubra) was set up using a sediment first spiked with the radioisotope 203Hg. Zinc concentrations (197-543 mg kg(-1) DM) in leaves were higher than Cu concentration (197-543 mg kg(-1) DM), Pb concentration (2.3-2.6 mg kg(-1) DM) and Hg concentration (0.9-1.7 mg kg(-1) DM). Leaves-to-sediment ratios decreased as follows: Zn > Cu > Hg > Pb. According to Ti measurements, metal contamination by dry deposition was less than 1%. Mercury concentration in plant leaves was higher than European and French thresholds. Foliar absorption of volatile Hg was a major pathway for Hg contamination with a root absorption of Hg higher in rape than in cabbage and red fescue. Growth of each species increased Cu solubility. Zinc solubility was increased only in the presence of rape. The highest increase of Cu solubility was observed for red fescue whereas this species largely decreased Zn solubility. Dissolved organic carbon (DOC) measurements suggested that Cu solubilisation could result from organic matter or release of natural plant exudates. Dissolved inorganic carbon (DIC) measures suggested that the high Zn solubility in the presence of rape could originate from a generation of acidity in rape rhizosphere and a subsequent dissolution of calcium carbonates. Consequently, emission of volatile Hg from contaminated dredged sediments and also the potential increase of metal solubility by a vegetal cover of grass when used in phytostabilisation must be taken into account by decision makers.

Biological Availability↗

Removal of Pb from a calcareous soil during EDTA-enhanced electrokinetic extraction.

Electrokinetic extraction has been tested to remove lead from an Algerian contaminated soil ([Pb] = 4.432 +/- 0.275 mg g(-1)) sited near a battery plant. The effect of EDTA at various concentrations (0.05-0.20 M) on the enhancement of lead transport has been studied by applying a constant voltage corresponding to a nominal electric field strength of 1 V cm(-1) (duration: 240 h). Results of contaminant distribution across the experimental cell have shown efficient transport of lead toward the anode despite the presence of calcite (25%) and the high acid/base buffer capacity of the soil. To avoid ligand loss, which would be anodically oxidized, the cell was modified by adding extra compartments and inserting cation exchange membranes (Neosepta CMX). Thus, simultaneous recovery of EDTA and lead from their chelated solutions has been made possible using the same set-up and by controlling fluids chemistry.

Cation Exchange Resins↗

Theoretical stability assessment of uranyl phosphates and apatites: selection of amendments for in situ remediation of uranium.

Addition of an amendment or reagent to soil/sediment is a technique that can decrease mobility and reduce bioavailability of uranium (U) and other heavy metals in the contaminated site. According to data from literature and results obtained in field studies, the general mineral class of apatites was selected as a most promising amendment for in situ immobilization/remediation of U. In this work we presented theoretical assessment of stability of U(VI) in four apatite systems (hydroxyapatite (HAP), North Carolina Apatite (NCA), Lisina Apatite (LA), and Apatite II) in order to determine an optimal apatite soil amendment which could be used for in situ remediation of uranium. In this analysis we used a theoretical criterion which is based on calculation of the ion-ion interaction potential, representing the main term of the cohesive energy of the matrix/pollutant system. The presented results of this analysis indicate (i) that the mechanism of immobilization of U by natural apatites depends on their chemical composition and (ii) that all analyzed apatites represent, from the point of view of stability, promising materials which could be used in field remediation of U-contaminated sites.

Adsorption↗