Overview and future trends in oil spill remote sensing

Remote sensing has great potential to provide data to improve oil spill response efforts. There are a number of sensors available that have been proven capable of detecting oil on water and measuring some of its properties. There is no single sensor that provides all the data needed, and hence a combination of sensors must be used. Even if finances and aircraft load capacity were unlimited, there are still many parameters of an oil slick that cannot be measured by remote sensing. This paper describes the cyrrently available sensors and their method of operation and outlines some new developments that have the potential to increase the amount of data available from an airborne remote sensing operation.     

Dynamic transformations of nitrogen during mechanical-biological pre-treatment of municipal solid waste

Mechanical-biological pre-treatment (MBP) of municipal solid waste (MSW) has gained evidence as a practice capable of accomplishing the requirements for environmental sustainable landfilling. In particular, MBP is effective in reducing the ammoniacal nitrogen content in the leachate. However, few data are available on the modifications of the nitrogen forms occurring during MBP and on the role played by processes such as nitrification and generation of refractory organic compounds. The dynamic transformations of nitrogen were investigated during the MBP. MSW was mechanically and biologically pre-treated; samples were collected at different stages of the process and analysed to investigate the evolution of nitrogen forms; batch and column leaching tests were performed as well. The results indicate that nitrification is negligible and volatilization can only partially explain the low ammoniacal nitrogen content in the leachate. Incorporation of ammoniacal nitrogen into a refractory organic form was assessed and is likely to play an important role. The maximum content of refractory organic nitrogen in the solid waste was achieved after about 60 days of aerobic pre-treatment; therefore, the minimal duration of the MBP should be about 8-9 weeks in order to optimize the ammoniacal nitrogen incorporation, unless the waste is characterized by a low C/N ratio.     

Preparation of Liquid Epoxidized Natural Rubber by Oxidative Degradations Using Periodic Acid,Potassium Permanganate and UV-Irradiation

Epoxidized natural rubber (ENR) needs to be degraded into shorter chain lengths, to form liquid epoxidized natural rubber (LENR), for applications such as coating and adhesives. Since ENR contains both C=C and epoxide groups as reactive sites for degradation reactions, thus, LENR could be prepared by different methods through cleavages of C=C or epoxide groups, or a combination of both sites. Different mechanisms would produce different terminals on the LENR. This paper reports the oxidative degradation by (a) periodic acid, (b) potassium permanganate and (c) ultra violet (UV) irradiation. The degraded rubbers were characterized by gel permeation chromatography (GPC), nuclear magnetic resonance (NMR) and Fourier transform infra-red spectroscopy (FTIR). Ester and ketone terminals were formed in all the three methods, but lactone and hydrofuranic structures were observed only in degradation by UV irradiation. NMR spectrum reveals that cyclization of ENR has occurred during degradation by periodic acid. At lower periodic acid concentration, degradation takes place only via C=C cleavage, but at higher concentration, the attack to the epoxide groups becomes more prominent. Potassium permanganate has attacked both the double bonds and epoxide groups. On the other hands, epoxide group was not affected during degradation by UV irradiation, which cleaved only the C=C bonds.     

Magnetic Cr(VI) Ion Imprinted Polymer for the Fast Selective Adsorption of Cr(VI) from Aqueous Solution

In this study, a novel magnetic Cr(VI) ion imprinted polymer (Cr(VI)-MIIP) was successfully synthesized and used as a selective sorbent for the adsorption of Cr(VI) ions from aqueous solution. It can be synthesized through the combination of an imprinting polymer and magnetic nanoparticles. The high selectivity achieved using MIIP is due to the specific recognition cavities for Cr(VI) ions created in Cr(VI)-MIIP. Also, the magnetic properties that could be obtained using magnetic nanoparticles, helps to separate adsorbent with an external magnetic field without either additional centrifugation or filtration procedures. The magnetic Fe₃O₄ nanoparticles (MNPs) were synthesized using an improved co-precipitation method and modified with tetraethylorthosilicate (TEOS) before imprinting. The magnetic Cr(VI) ion imprinted polymer was prepared through precipitation copolymerization of 4-vinylpyridine as the complexing monomer, 2-hydroxyethyl methacrylate as a co-monomer, the Cr⁶⁺ anion as a template, and ethylene glycol dimethacrylate (EGDMA) as a cross-linker in the presence of modified magnetite nanoparticles. This novel synthesized sorbent was characterized using different techniques. Batch adsorption experiments were performed to evaluate the adsorption conditions, selectivity, and reusability. The results showed that the maximum adsorption capacity was 39.3 mg g^?1, which was observed at pH 3 and at 25?°C. The equilibrium time was 20 min, and the amount of adsorbent which gave the maximum adsorption capacity was 1.7 g L^?1. Isotherm studies showed that the adsorption equilibrium data were fitted well with the Langmuir adsorption isotherm model and the theoretical maximum adsorption capacity was 44.86 mg g^?1. The selectivity studies indicated that the synthesized sorbent had a high single selectivity sorption for the Cr(VI) ions in the presence of competing ions. Thermodynamic studies revealed that the adsorption process was exothermic (\(\Delta H\)?<?0) and spontaneous (\(\Delta G\)?<?0). In addition, the spent MIIP can be regenerated up to five cycles without a significant decrease in adsorption capacity.     

Groundwater geochemistry diagnostics during in situ ERH remediation

In situ remediation represents a series of challenges in interpreting the monitoring data on remedial progress. Among these challenges are problems in determining the progress of the remediation and the mechanisms responsible, so that the process can be optimized. The release of organic pollutants to groundwater systems and in situ remediation technologies alter the groundwater chemistry, but outside of natural attenuation studies using inorganic chemical analyses as indicators of intrinsic biodegradation, typically little attention has been paid to the changes in inorganic groundwater chemistry. Smith (2008) noted that during an electrical resistance heating remediation that took place at a confidential site in Chicago, a two‐orders‐of‐magnitude increase in chloride concentrations occurred during the remediation. This increase in chloride resulted in a corresponding increase in calcium as a result of what is known as the common ion effect. Carbon dioxide is the gas found in highest concentrations in natural groundwater (Stumm & Morgan, 1981), and its fugacity (partial pressure) corresponds directly with calcium concentrations. Carbon dioxide at supersaturation in groundwater is capable of dissolving organic compounds, such as trichloroethene, facilitating removal of nonaqueous‐phase liquids at temperatures below the boiling point of water. One means of diagnosing these reactions is through the use of compound‐specific isotopic analysis, which is capable of distinguishing between evaporation, biodegradation, and differences in sources. The appropriate diagnosis has the potential to optimize the benefits from these reactions, lower energy costs for removal of nonaqueous‐phase liquids, and direct treatment where it is needed most. © 2010 Wiley Periodicals, Inc.     

Technology review and evaluation of different chemical oxidation conditions on treatability of PFAS

Per‐ and polyfluoroalkyl substances (PFAS) are a class of stable compounds widely used in diverse applications. These emerging contaminants have unique properties due to carbon–fluorine (C–F) bonds, which are some of the strongest bonds in chemistry. High energy is required to break C–F bonds, which results in this class of compounds being recalcitrant to many degradation processes. Many technologies studied that have shown treatment effectiveness for PFAS cannot be implemented in situ. Chemical oxidation is a demonstrated remediation technology for in situ treatment of a wide range of organic environmental contaminants. An overview of relevant literature is presented, summarizing the use of single or combined reagent chemical oxidation processes that offer insight into oxidation–reduction chemistries potentially capable of PFAS degradation. Based on the observations and results of these studies, bench‐scale treatability tests were designed and performed to establish optimal conditions for the formation of specific free radical species, including superoxide and sulfate radicals, via various combinations of oxidants, catalysts, pH buffers, and heat to assess PFAS treatment by chemical oxidants. The study also suggests the possible abiotic transformations of some PFAS when chemical oxidation is or was used for treatment of primary organic contaminants (e.g., petroleum or chlorinated organic compounds) at a site. The bench‐scale tests utilized field‐collected samples from a firefighter training area. Much of the available data related to chemical oxidation of PFAS has only been reported for one or both of the two more commonly discussed PFAS (perfluorooctane sulfonic acid and/or perfluorooctanoic acid). In contrast, this treatability study evaluates oxidation of a diverse list of PFAS analytes. The results of this study and published literature conclude that heat‐activated persulfate is the oxidation method with the best degradation of PFAS. Limited reduction of reported PFAS concentrations in this study was observed in many oxidation reactors; however, unknown mass of PFAS (such as precursors of perfluoroalkyl acids) that cannot be identified in a field collected sample complicated quantification of how much oxidative destruction of PFAS actually occurred.     

Production of biologically safe digested manure for land application by a full-scale biogas plant with heat-inactivation

Inactivation of indigenous indicator micro-organisms such as faecal coliforms, coliphages, and faecal streptococci was investigated in a full-scale biogas plant that mainly digested cow manure. The biogas plant consisted principally of a feed reservoir, fermentation tank (37 degrees C), heat-inactivation process (70 degrees C), and five reservoirs for the heat-inactivated, digested manure that was used by a local livestock farmer as liquid fertilizer. Although all the indicators tended to exhibit stepwise decreases with each stage of treatment, coliphages were found to be more capable of surviving than faecal coliforms and faecal streptococci under mesophilic anaerobic conditions as well as high temperature conditions (heat-inactivation at 70 degrees C). Liquid fertilizer produced at the biogas plant had faecal coliform densities less than the stipulations of the US EPA 40 CFR 503 Class A limits. Heat-inactivation tests indicated that although coliphages exhibited more tolerance than other bacterial indicators between 37 and 70 degrees C, they were more sensitive to continuous temperature increase than faecal coliforms and faecal streptococci.     

MSWI boiler fly ashes: magnetic separation for material recovery

Nowadays, ferrous materials are usually recovered from Municipal Solid Waste Incineration (MSWI) bottom ash by magnetic separation. To our knowledge, such a physical technique has not been applied so far to other MSWI residues. This study focuses thus on the applicability of magnetic separation on boiler fly ashes (BFA). Different types of magnet are used to extract the magnetic particles. We investigate the magnetic particle composition, as well as their leaching behaviour (EN 12457-1 leaching test). The magnetic particles present higher Cr, Fe, Mn and Ni concentration than the non-magnetic (NM) fraction. Magnetic separation does not improve the leachability of the NM fraction. To approximate industrial conditions, magnetic separation is also applied to BFA mixed with water by using a pilot. BFA magnetic separation is economically evaluated. This study globally shows that it is possible to extract some magnetic particles from MSWI boiler fly ashes. However, the magnetic particles only represent from 23 to 120 g/kg of the BFA and, though they are enriched in Fe, are composed of similar elements to the raw ashes. The industrial application of magnetic separation would only be profitable if large amounts of ashes were treated (more than 15 kt/y), and the process should be ideally completed by other recovery methods or advanced treatments.     

Enhancing performance and durability of slag made from incinerator bottom ash and fly ash

This work presents a method capable of melting the incinerator bottom ash and fly ash in a plasma furnace. The performance of slag and the strategies for recycling of bottom ash and fly ash are improved by adjusting chemical components of bottom ash and fly ash. Ashes are separated by a magnetic process to improve the performance of slag. Analytical results indicate that the air-cooled slag (ACS) and magnetic-separated slag (MSS) have hardness levels below 590 MPa, indicating fragility. Additionally, the hardness of crystallized slag (RTS) is between 655 and 686 MPa, indicating toughness. The leached concentrations of heavy metals for these three slags are all below the regulatory limits. ACS appears to have better chemical stability than MSS, and is not significantly different from RTS. In the potential alkali-silica reactivity of slag, MSS falls on the border between the harmless zone and the potentially harmful zone. ACS and RTS fall in the harmless zone. Hence, the magnetic separation procedure of ashes does not significantly improve the quality of slag. However, RTS appears to improve its quality.     

A Review of the Status of Advanced Technologies for the Detection of Oil in and with Ice

Remote sensors for application to oil in ice and oil with ice are assessed. Radio-frequency methods to detect oil in ice depend on the difference in dielectric properties between oil and water. Freshwater ice is relatively transparent to frequencies below about 200 MHz. Despite extensive theoretical studies, there is a lack of experimental evidence to support the notion that radio-frequency methods have potential.Acoustic methods for the detection of oil in ice show promise. Regular metal inspection equipment is capable of detecting oil layers under ice. Oil propagates shear waves and detection methods based on this unique property are capable of identifying oil in ice. One unit has been built and tested in the field based on this principle.Oil with ice detection is a well developed technology. A common sensor is an infrared camera or an IR/UV (infrared/ultraviolet) system. The inherent weaknesses include the inability to discriminate oil on beaches, among weeds or debris. The laser fluorosensor is a most useful instrument because of its unique ability to identify oil on backgrounds that include water, soil, ice and snow. It is the only sensor that can positively discriminate oil on most backgrounds. Radar offers the only potential for large area searches and foul weather remote sensing, however, there is little potential to detect oil in the immediate vicinity of ice. A major weakness of radar is that it is limited to operation over seas with winds of about 2–8 m/s.Equipment operating in the visible region of the spectrum, such as cameras and scanners, is useful for documentation or providing a basis for the overlay of other data. It is not useful beyond this because oil shows no spectral characteristics in the visible region that can be used to discriminate oil.     

An environmental analysis for comparing waste management options and strategies

The debate on different waste management practices has become an issue of utmost importance as human activities have overloaded the assimilative capacity of the biosphere. Recent Italian law on solid waste management recommends an increase in material recycling and energy recovery, and only foresees landfill disposal for inert materials and residues from recovery and recycling. A correct waste management policy should be based on the principles of sustainable development, according to which our refuse is not simply regarded as something to eliminate but rather as a potential resource. This requires the creation of an integrated waste management plan that makes full use of all available technologies. In this context, eMergy analysis is applied to evaluate three different forms of waste treatment and construct an approach capable of assessing the whole strategy of waste management. The evaluation included how much investment is needed for each type of waste management and how much "utility" is extracted from wastes, through the use of two indicators: Environmental yield ratio (EYR) and Net eMergy. Our results show that landfill is the worst system in terms of eMergy costs and eMergy benefits. Composting is the most efficient system in recovering eMergy (highest EYR) from municipal solid waste (MSW) while incineration is capable of saving the greatest quantity of eMergy per gram of MSW (highest net eMergy). This analysis has made it possible to assess the sustainability and the efficiency of individual options but could also be used to assess a greater environmental strategy for waste management, considering a system that might include landfills, incineration, composting, etc.     

Removal of Cinnamic Acid Derivatives from Aqueous Effluents by Fenton and Fenton-like Processes as an Alternative to Direct Biological Treatment

The removal of various phenolic acids (p-coumaric, caffeic and ferulic acids), typically found in wastewaters of agricultural origin, from model effluents by chemical and biological means has been investigated. Chemical oxidation processes comprising hydrogen peroxide and a homogeneous or heterogeneous copper or iron catalyst were employed over a wide range of experimental conditions. Chemical oxidation is capable of removing most of the total organic carbon initially present in the effluent at relatively mild treatment conditions (i.e. reaction times up to 120 min and temperatures up to 80°C), while removal rates generally increase with increasing temperature, H₂O₂ and catalyst concentrations. The anaerobic degradability and toxicity of p-coumaric acid has been assessed using the biochemical methane potential and anaerobic toxicity assay respectively. p-Coumaric acid, at concentrations below about 1 g/L, is not toxic against methanogens and slowly degrades over a period of about 35 days at 35°C. In light of this, chemical oxidation may provide a promising alternative to direct biological treatment for either the partial or complete removal of phenolic acids at reasonable treatment times; the implications for wastewater treatment are discussed.     

Stimulation of aerobic degradation of chlorinated ethenes in soil by microbial inoculation

Degradation of chlorinated ethenes under aerobic conditions has been reported using a cometabolic pathway. A site in Illinois had shallow contamination and sandy soils, which in combination created aerobic conditions. The aerobic conditions prevented the degradation of chlorinated ethenes by reductive dechlorination. Biodegradation of chloroethenes under aerobic conditions does not occur naturally at all sites; however, it can be enhanced if microorganisms capable of cometabolic degradation are introduced into the soil. In this study, trichloroethene (TCE) removal in the soil was enhanced by the injection of a commercially available microbial inoculum (CL‐OUT® inoculum, CL‐Solutions, Cincinnati, OH) and nutrients and was compared to chlorinated ethene removal in soil that had received nutrients only and soil that had received activated sludge and nutrients. Trichloroethene removal was measured after one week, seven weeks, and eleven weeks. After one week, no significant TCE removal had occurred in any of the test microcosms. After seven weeks, a slight decrease in TCE levels accompanied by an increase in cis‐1,2‐dichloroethene (cis‐1,2‐DCE) was seen in the microcosms that had received CL‐OUT®. After 11 weeks, a marked decrease in TCE levels was observed in the microcosms that had received CL‐OUT®. No significant TCE decrease was observed in any of the other microcosms. These data suggest that organisms capable of aerobic TCE degradation were not present at the site; however, the addition of an inoculum containing such organisms enabled aerobic degradation to occur. © 2008 Wiley Periodicals, Inc.     

Phytoremediation of landfill leachate

Leachate emissions from landfill sites are of concern, primarily due to their toxic impact when released unchecked into the environment, and the potential for landfill sites to generate leachate for many hundreds of years following closure. Consequently, economically and environmentally sustainable disposal options are a priority in waste management. One potential option is the use of soil-plant based remediation schemes. In many cases, using either trees (including short rotation coppice) or grassland, phytoremediation of leachate has been successful. However, there are a significant number of examples where phytoremediation has failed. Typically, this failure can be ascribed to excessive leachate application and poor management due to a fundamental lack of understanding of the plant-soil system. On balance, with careful management, phytoremediation can be viewed as a sustainable, cost effective and environmentally sound option which is capable of treating 250m(3)ha(-1)yr(-1). However, these schemes have a requirement for large land areas and must be capable of responding to changes in leachate quality and quantity, problems of scheme establishment and maintenance, continual environmental monitoring and seasonal patterns of plant growth. Although the fundamental underpinning science is well understood, further work is required to create long-term predictive remediation models, full environmental impact assessments, a complete life-cycle analysis and economic analyses for a wide range of landfill scenarios.     

Bioremediation of Dissolved and Free Phase Oil in Wastewater from Equipment Maintenance Activities

Land treatment facilities can provide effective treatment of secondary oily wastewater from maintenance operations, particularly in arid climates. Soil and underlying groundwater from a land treatment facility, which has been operating for eight years, were analyzed to determine the effectiveness of using bioremediation for the treatment of dissolved and free‐phase oil in maintenance wastewater. The study was conducted at a mining site in Western Australia. The facility was capable of treating 140 kiloliters (kL) of oily wastewater per day. The average petroleum hydrocarbon content of the wastewater was 2 percent weight per volume (w/v) based on data available for the first five years. The soil data indicate that the land treatment process has been operating efficiently even at high wastewater loadings with maximum degradation rates of 10–242 mg/kg per day. Based on the soil data, there is no evidence of accumulation of any metal or polycyclic aromatic hydrocarbon (PAH) compounds. The land treatment facility has led to only low levels of TPH (total petroleum hydrocarbons) contamination (<4 ppm) in the underlying groundwater. However, nitrate concentrations in the groundwater were shown to increase over the first five years of the facility's operation. This article reports and discusses the operational data from the land treatment process, illustrating its effectiveness in treating oily wastewater. © 2001 John Wiley & Sons, Inc.     

A Novel Approach to Biological Treatment of Contaminated Water

Over the past few years, the focus of our research has been to respond to the recognized needs for novel biological processes that are capable of destroying a wide range of biodegradable pollutants and providing the perfect environment for complex interspecies interactions required for the degradation of environmental contaminants. A new biotechnology process called Biological Permeable Barrier (BPB) was developed to provide high microbial density, stable environmental conditions, and protective measures for microbial activities for in‐situ bioremediation of contaminated groundwater. This patented technology (U.S. Patent 6,337,019 ) is based on the creation of a structured matrix, or Bio‐beads, that provides the perfect environment for organic‐degrading microorganisms to establish biofilms capable of destroying the contaminants in water with remarkable stability and control. For over 240 days, the viability and performance of the BPB (Bio‐beads) system were shown for biodegradation of a targeted contaminant, 2,4,6‐ trichlorophenol (TCP), under a variety of operating and stress conditions (Razavi‐Shirazi, 1997 ). Extensive batch experiments were also conducted to obtain necessary data to determine the rate of TCP diffusion into the Bio‐beads, adsorption properties of the Bio‐beads, and substrate‐use rate of the mixed bioculture as free cells and as immobilized cells (Bio‐beads). A simulated model of BPB was also characterized with its porosity, permeability, and compressibility or deformation under typical field conditions. Our extensive research showed that BPB takes advantage of a controlled biotechnology process to overcome the disadvantages and uncertainties associated with conventional biological processes. A summary of our investigation is presented here. © 2002 Wiley Periodicals, Inc.     

Application of magnetic separation to steelmaking slags for reclamation

Integrated iron and steel plants generate large amounts of metallurgical slag, which usually contains some quantity of metals or mixtures of oxides that could be treated to be recycled in various applications. The conventional method for disposal of slags is dumping. However, it is possible to process the slags to be used in the production of metallic iron, or as an additive in cement making. In this study, a basic oxygen furnace (BOF) steelwork slag obtained from the Kardemir integrated iron and steel works, Karabuk, Turkey is used. A drum magnetic separator system with pre-engineered crucial processing parameters of drum revolution speed, drum radius, drum flesh thickness, and magnitude of the magnetic field applied is utilized, as these parameters have a competing influence on the results. Subsequently, the effects of slag grain size and the drum-blade gap are investigated in the separation efficiency of magnetic grains. It is found that collection of magnetic grains is improved by decreasing the grain size of slags and moreover, the collection of magnetic grains fraction is increased with an increase in the gap between the blades and drum.     

Evaluation of XRF and LIBS technologies for on-line sorting of CCA-treated wood waste

Contamination of wood waste with chromated copper arsenate greatly limits recycling opportunities for the wood waste as a whole. Separation of CCA-treated wood from other wood types is one means by which such contamination can be removed. The purpose of the current study was to evaluate two detector technologies for sorting CCA-treated wood from other wood types. The detector technologies evaluated included X-ray fluorescence spectroscopy (XRF) and laser induced breakdown spectroscopy (LIBS). The XRF detector system utilized in this study was capable of rapidly detecting the presence of CCA in painted wood, wet wood, heartwood, sapwood, and at portions of the wood containing knots. Furthermore, the XRF system was capable of distinguishing between CCA-treated wood and wood treated with alternative wood treatment preservatives, but was limited by the fact that it was not designed for on-line operation so tests were conducted in a batch mode on a conveyor. The analysis time used in this study (3 s) can be decreased significantly for an XRF system designed specifically for on-line operation. The LIBS system developed for this study was found to effectively identify CCA-treated wood for pieces ranging in thickness from 1 to 8 cm. High sorting efficiencies were noted when 10 laser shots were taken on a piece of wood. Furthermore, the LIBS system was found to be effective for identifying wood that has been coated with stains and paints in addition to identifying wood that has been CCA treated. The major drawback with the LIBS system developed in this study was the limited laser pulse energy. With an increase in laser pulse energy it is anticipated that the working focal length of the LIBS system can be increased to enable the monitoring of wood samples of more variable thicknesses. Limitations associated with analysis of very rotted pieces of wood and wet wood can also be overcome by using a higher pulse energy laser. Overall, both technologies show incredible promise for sorting CCA-treated wood from other wood types. The next recommended step would be to run an improved full-scale operation at one facility to document sorting efficiencies and fine-tune the improvements proposed in the current study. Such a study could potentially open-the-door for more widespread sorting of wood waste.