Raffaella Pomi

Management of municipal solid waste incineration residues

The management of residues from thermal waste treatment is an integral part of waste management systems. The primary goal of managing incineration residues is to prevent any impact on our health or environment caused by unacceptable particulate, gaseous and/or solute emissions. This paper provides insight into the most important measures for putting this requirement into practice. It also offers an overview of the factors and processes affecting these mitigating measures as well as the short- and long-term behavior of residues from thermal waste treatment under different scenarios. General conditions affecting the emission rate of salts and metals are shown as well as factors relevant to mitigating measures or sources of gaseous emissions.

A review of dark fermentative hydrogen production from biodegradable municipal waste fractions

Hydrogen is believed to play a potentially key role in the implementation of sustainable energy production, particularly when it is produced from renewable sources and low energy-demanding processes. In the present paper an attempt was made at critically reviewing more than 80 recent publications, in order to harmonize and compare the available results from different studies on hydrogen production from FW and OFMSW through dark fermentation, and derive reliable information about process yield and stability in view of building related predictive models. The review was focused on the effect of factors, recognized as potentially affecting process evolution (including type of substrate and co-substrate and relative ratio, type of inoculum, food/microorganisms [F/M] ratio, applied pre-treatment, reactor configuration, temperature and pH), on the fermentation yield and kinetics. Statistical analysis of literature data from batch experiments was also conducted, showing that the variables affecting the H2 production yield were ranked in the order: type of co-substrate, type of pre-treatment, operating pH, control of initial pH and fermentation temperature. However, due to the dispersion of data observed in some instances, the ambiguity about the presence of additional hidden variables cannot be resolved. The results from the analysis thus suggest that, for reliable predictive models of fermentative hydrogen production to be derived, a high level of consistency between data is strictly required, claiming for more systematic and comprehensive studies on the subject.

Properties of Portland cement - Stabilised MSWI fly ashes

In the present paper, the properties of Portland cement mixtures containing fly ashes (FA) collected at four different Italian municipal solid waste incineration (MSWI) plants were investigated. In particular, physical/mechanical characteristics (setting time, unconfined compressive strength (UCS) and shrinkage/expansion), as well as the acid neutralisation behaviour of the solidified products were considered. The FA composition, revealing enrichment in heavy metals, chlorides and sulphates, significantly altered the hydration behaviour of Portland cement. Consequently, for some of the investigated FA the maximum allowable content for the mixtures to achieve appreciable mechanical strength was 20 wt.%. Even at low FA dosages setting of cement was strongly delayed. In order to improve the properties of FA/cement mixtures, the use of additives was tested.Moreover, the acid neutralisation capacity (ANC) of the solidified products was evaluated in order to assess the ability of the matrix to resist acidification, and also to provide information on hydration progression, as well as on heavy metal release under different pH conditions. Comparison of the results from the present work with previous studies carried out on spiked mixtures lead to the conclusion that the mechanical properties of the stabilised FA could not be predicted based on the effect exerted by heavy metals and anions only, even when the dilution effect exerted on cement was taken into account. It was likely that a major role was also played by alkalis, which were present in the FA at much higher concentrations than in cement.

ENHANCED ELECTROKINETIC TREATMENT OF MARINE SEDIMENTS CONTAMINATED BY HEAVY METALS AND PAHS

Dredged sediments contaminated by heavy metals and PAHs were subjected to both unenhanced and enhanced electrokinetic remediation under different operating conditions, obtained by varying the applied voltage and the type of conditioning agent used at the electrode compartments in individual experiments. While metals were not appreciably mobilized as a result of the unenhanced process, metal removal was found to be significantly improved when both the anodic and cathodic reservoirs were conditioned with the chelating agent EDTA, with removal yields ranging from 28% to 84% depending on the contaminant concerned. As for the effect on organic contaminants, under the conditions tested the electrokinetic treatment displayed a poor removal capacity towards PAHs, even when a surfactant (Tween 80) was used to promote contaminant mobilization, indicating the need for further investigation on this issue. Further research on organics removal from this type of materials through electrokinetic remediation is thus required. Furthermore, a number of technical and environmental issues will also require a careful evaluation with a view to full-scale implementation of electrokinetic sediment remediation. These include controlling side effects during the treatment (such as anodic precipitation, oxidation of the conditioning agent, and evolution of toxic gases), as well as evaluating the potential ecotoxicological effects of the chemical agents used.

Accelerated carbonation of different size fractions of bottom ash from RDF incineration

This paper investigates the effects of accelerated carbonation on the characteristics of bottom ash from refuse derived fuel (RDF) incineration, in terms of CO(2) uptake, heavy metal leaching and mineralogy of different particle size fractions. Accelerated aqueous carbonation batch experiments were performed to assess the influence of operating parameters (temperature, CO(2) pressure and L/S ratio) on reaction kinetics. Pressure was found to be the most relevant parameter affecting the carbonation yield. This was also found to be largely dependent on the specific BA fraction treated, with CO(2) uptakes ranging from approximately 4% for the coarse fractions to approximately 14% for the finest one. Carbonation affected both the mineralogical characteristics of bottom ash, with the appearance of neo-formation minerals, and the leaching behaviour of the material, which was found to be mainly related to the change upon carbonation in the natural pH of the ash.

The effects of accelerated carbonation on CO2 uptake and metal release from incineration APC residues

This work presents the results of a study on accelerated carbonation of incinerator air pollution control residues, with a particular focus on the modifications in the leaching behaviour of the ash. Aqueous carbonation experiments were carried out using 100% CO(2) at different temperatures, pressures and liquid-to-solid ratios, in order to assess their influence on process kinetics, CO(2) uptake and the leaching behaviour of major and trace elements. The ash showed a particularly high reactivity towards CO(2), owing to the abundance of calcium hydroxides phases, with a maximum CO(2) uptake of approximately 250g/kg. The main effects of carbonation on trace metal leaching involved a significant decrease in mobility for Pb, Zn and Cu at high pH values, a slight change or mobilization for Cr and Sb, and no major effects on the release of As and soluble salts. Geochemical modelling of leachates indicated solubility control by different minerals after carbonation. In particular, in the stability pH range of carbonates, solubility control by a number of metal carbonates was clearly suggested by modelling results. These findings indicate that accelerated carbonation of incinerator ashes has the potential to convert trace contaminants into sparingly soluble carbonate forms, with an overall positive effect on their leaching behaviour.

Acid neutralisation capacity and hydration behaviour of incineration bottom ash-Portland cement mixtures

Abstract The present paper deals with the use of incineration bottom ash in cementitious systems. The results of the physical–mechanical characterisation of the solidified products were discussed elsewhere, while the present work focuses on the acid neutralisation capacity (ANC) of the investigated mixtures as a means to evaluate the type of hydration products and their relative amounts in the solid matrix. The approach consists of differential acid neutralisation analysis, which was validated using traditional X-ray diffraction (XRD) methods.

Mechanical properties and leaching modeling of activated incinerator bottom ash in Portland cement blends

In the present study the evolution of mechanical strength and the leaching behavior of major and trace elements from activated incinerator bottom ash/Portland cement mixtures were investigated. Chemical and mechanical activation were applied with the purpose of improving the reactivity of bottom ash in cement blends. Chemical activation made use of NaOH, KOH, CaCl(2) or CaSO(4), which were selected for the experimental campaign on the basis of the results from previous studies. The results indicated that CaCl(2) exhibited by far the best effects on the evolution of the hydration process in the mixtures; a positive effect on mechanical strength was also observed when CaSO(4) was used as the activator, while the gain in strength produced by KOH and NaOH was irrelevant. Geochemical modeling of the leaching solutions provided information on the mineral phases responsible for the release of major elements from the hardened materials and also indicated the important role played by surface sorption onto amorphous Fe and Al minerals in dictating the leaching of Pb. The leaching of the other trace metal cations investigated (Cu, Ni and Zn) could not be explained by any pure mineral included in the thermodynamic database used, suggesting they were present in the materials in the form of complex minerals or phase assemblages for which no consistent thermodynamic data are presently available in the literature.

Genetic algorithms as a promising tool for optimisation of the MSW collection routes

Important advantages, including reductions in fuel consumption and labour cost, arise from the optimal design of solid waste (SW) collection routes. Further, optimal design can reduce vehicle maintenance expenditures and improve traffic conditions in urban areas. To date, optimal routes have been developed according to intuitive methodologies and field experience. However, increasing attention is being devoted to innovative approaches, such as those able to simulate complex collection systems. To analyse these complexities, operational research applications are used. They are typically based on the implementation of heuristic procedures allowing for high quality solutions to the problem at hand. From a computational point of view, however, heuristic procedures have a complexity which is o(n3), where n is the number of points which have to be visited during each route. This is a limit for an accurate representation of urban areas and for the quality of the calculated solutions. An alternative methodology, which is the subject of this paper, is based on a genetic algorithm. Also, an ad hoc algorithm, developed in the framework of a wider research, is illustrated. Results of a preliminary field test conducted for verification are also presented.

Effects of thin-film accelerated carbonation on steel slag leaching

This paper discusses the effects of accelerated carbonation on the leaching behaviour of two types of stainless steel slags (electric arc furnace and argon oxygen decarburisation slag). The release of major elements and toxic metals both at the natural pH and at varying pH conditions was addressed. Geochemical modelling of the eluates was used to theoretically describe leaching and derive information about mineralogical changes induced by carbonation. Among the investigated elements, Ca and Si were most appreciably affected by carbonation. A very clear effect of carbonation on leaching was observed for silicate phases; geochemical modelling indicated that the Ca/Si ratio of Ca-controlling minerals shifted from ∼ 1 for the untreated slag to 0.5-0.67 for the carbonated samples, thus showing that the carbonation process left some residual Ca-depleted silicate phases while the extracted Ca precipitated in the form of carbonate minerals. For toxic metals the changes in leaching induced by carbonation appeared to be mainly related to the resulting pH changes, which were as high as ∼ 2 orders of magnitude upon carbonation. Depending on the specific shape of the respective solubility curves, the extent of leaching of toxic metals from the slag was differently affected by carbonation.