Immobilisation of beryllium in solid waste (red-mud) by fixation and vitrification

The objective of this study was to obtain information on the immobilization of beryllium (Be) in solid waste generated in the extraction process of beryllium from its ore, Beryl. This solid waste, termed red-mud, contains oxides of iron, aluminium, calcium, magnesium and beryllium. The red-mud waste contains beryllium at levels above the permissible limit, which prevents its disposal as solid waste. The total beryllium content in the red-mud analysed showed value ranging from 0.39 to 0.59% Be The studies showed that 50% of the total beryllium in red-mud can be extracted by water by repeated leaching over a period of 45 days. The cement mix, casting into cement blocks, was subjected to leachability studies over a period of 105 days and immobilization factor (IF factor) was determined. These IF values, of the order of 102, were compared with those obtained by performing leachability study on vitrified red-mud masses produced at different temperature conditions. Direct heating of the red-mud gave the gray coloured, non-transparent vitreous mass (as 'bad glass') showed effective immobilisation factor for beryllium in red-mud of the order of 10(4).     

Natural Weathering of Polypropylene and Waste Tire Dust (PP/WTD) Blends

Three series of polypropylene and waste tire dust (PP/WTD) blends using three different WTD sizes were prepared, compression-molded and cut into dumbbells. The specimens were exposed to natural weathering in the northern part of Malaysia for a period of 6 months. The results show that at the same blend composition, blends with fine WTD size exhibit higher mechanical properties than that of blends with coarse WTD after exposure to natural weathering. Regardless of WTD size, the retention of tensile strength and elongation at break, E_b increases with the increase in WTD content. From the exposed surface morphology, it is apparent that the blends with fine WTD and WTD-rich blends were able to withstand weathering better than blends with coarse WTD and PP-rich blends. The DSC thermograms suggest that the overall drop in melting temperature (T_m) of the exposed blends decreases as the WTD content increases.     

Brominated flame retardants and heavy metals in automobile shredder residue (ASR) and their behavior in the melting process

The End-of-life Vehicles Recycling Act went into effect on January 1, 2005, in Japan and requires the proper treatment of airbags, chlorofluorocarbons (CFCs), and automobile shredder residue (ASR). The need for optimal treatment and recycling of ASR, in particular, has been increasing year after year because ASR is regarded as being difficult to treat. Dioxin-related compounds, brominated flame retardants (BFRs), heavy metals, chlorine and organotin compounds are all present in high concentrations in ASR. The authors conducted ASR melting treatment tests using a 10-tons/day-scale direct melting system (DMS), which employs shaft-type gasification and melting technology. The results obtained showed that dioxin-related compounds and BFRs were decomposed by this melting treatment. The high-temperature reducing atmosphere in the melting furnace moved volatile heavy metals such as lead and zinc into the fly ash where they were distributed at a rate of more than 90% of the input amount. This treatment was also found to be effective in the decomposition of organotin, with a rate of decomposition higher than 99.996% of the input amount. Via the recovery of heavy metals concentrated in the fly ash, all the products discharged from this treatment system were utilized effectively for the complete realization of an ASR recycling system that requires no final disposal sites.     

An alternative method for the treatment of waste produced at a dye and a metal-plating industry using natural and/or waste materials.

The aim of this study was to develop cost-effective, appropriate solidification technologies for treating hazardous industrial wastes that are currently disposed of in ways that may threaten the quality of local groundwater. One major objective was to use materials other than cement, and preferably materials that are themselves wastes, as the solidification additives, namely using wastes to treat wastes or locally available natural material. This research examines the cement-based and lime-based stabilization/solidification (S/S) techniques applied for waste generated at a metal-plating industry and a dye industry. For the lime-based S/S process the following binder mixtures were used: cement kiln dust/ lime, bentonite/lime and gypsum/lime. For the cement-based S/S process three binder mixtures were used: cement kiln dust/cement, bentonite/cement and gypsum/cement. The leachability of the wastes was evaluated using the toxicity characteristic leaching procedure. The applicability and optimum weight ratio of the binder mixtures were estimated using the unconfined compressive strength test. The optimum ratio mixtures were mixed with waste samples in different ratios and cured for 28 days in order to find the S/S products with the highest strength and lowest leachability at the same time. The results of this work showed that the cement-and lime-based S/S process, using cement kiln dust and bentonite as additives can be effectively used in order to treat industrial waste.     

Decomposition of hazardous organic materials in the solidification/stabilization process using catalytic-activated carbon

The application of a catalytic-activated carbon to the solidification/stabilization (S/S) process for immobilization of phenol and 2-chlorophenol and catalytic decomposition was investigated. The effect of the catalytic-activated carbon, in amounts of 0.25-1% (by dry sand wt.), on the leaching of phenol and 2-chlorophenol was studied. H2O2 was added as a source of oxygen in the amounts of 1 or 5%, with respect to liquid solution weight. Toxicity characteristic leaching procedure (TCLP) leaching tests showed that adding the catalytic-activated carbon to the S/S matrix significantly reduced the leachability of both phenol and 2-chlorophenol. Only trace amounts of phenol were found in the leaching solution, while the concentration of 2-chlorophenol was below the detection limit of the gas chromatography (GC). Without addition of the catalytic-activated carbon, 87% of the phenol and 92% of the 2-chlorophenol leached. Additional tests on TCLP leachate solutions using GC-mass spectrometry indicated the existence of simple, less hazardous, hydrocarbons, including alcohol. Catalytic-activated carbons treated with phenol in the presence of H2O2 were also analyzed using time of flight-secondary ion mass spectroscopy (TOF-SIMS). Results indicate that the phenol aromatic ring was broken by the catalytic reaction.     

Effect of polyethylene terephthalate (PET) on the pyrolysis of brominated flame retardant-containing high-impact polystyrene (HIPS-Br)

Pyrolysis of brominated flame retardant-containing high-impact polystyrene (HIPS-Br) was performed at 430°C in the presence of 0.1 wt% of polyethylene terephthalate (PET) in a Pyrex glass reactor. Two different types of brominated flame retardants (decabromodiphenyl ether and decabromodiphenyl ethane) with or without antimony trioxide (as synergist) 5 wt% were used. The presence of PET had a significant effect on the material balance, decreasing the gaseous product and increasing the residue. The type of flame retardant had no effect on the yield of liquid product; however, the presence of Sb resulted in a marked difference in the distribution of decomposition products. Analysis by a gas chromatograph equipped with a flame ionization detector showed that the hydrocarbons were distributed in the range n-C₇ to n-C₂₅ with major peaks at n-C₉ and n-C₁₇. The presence of PET increased the formation of brominated compounds by several times and affected both the type and quantity of polybrominated compounds. The liquid products obtained from the pyrolysis of HIPS-Br/PET have to be treated before they can be used     

Production and characterization of KOH-activated carbon derived from polychlorinated biphenyl residue generated by the sodium dispersion process

Polychlorinated biphenyl (PCB) residues from the sodium dispersion (SD) process were employed as the raw materials for the production of activated carbon using KOH activation. The pore properties, such as the specific surface area and pore size distribution, were characterized using the Barrett–Joyner–Halenda method and the Horvath–Kawazoe method based on the N₂ adsorption isotherm at 77 K. The activated carbon produced showed similar adsorption capacities and specific surface areas to the commercially available product. The effects of the activation conditions on the porosity of the activated carbon produced were studied. The most significant factor affecting the specific surface proved to be the activation temperature. The activated carbon produced from PCB residues from the high-temperature (423–443 K) SD process had a binary pore size distribution well developed in the 4 nm region and in the micropore region. The pore structure of the carbon produced from PCB residues from the low-temperature (333–393 K) SD process had a wide range of micropores and mesopores.     

The basic properties of poly(lactic acid) produced by the direct condensation polymerization of lactic acid

Poly(lactic acids) with high molecular weights have been synthesized by direct condensation polymerization of lactic acid. These polymers have good mechanical properties and can be processed into products such as cups, film, and fiber, which can be used as compostable materials. This polymerization method can be applied to the synthesis of copolymers of lactic acid and other hydroxyacids. The properties of poly(lactic acid) and copolymers synthesized by the direct process are different from those of polymers obtained by the conventional lactide process.     

Adsorption removal of pollutants by active cokes produced from sludge in the energy recycle process of wastes

This study proposes a recycling system of sludge into active cokes and the fundamental examinations for the application were carried out. In the system, active cokes were produced by carbonizing pellets of sludge in a steam stream. Pyrolysis gas yielded by carbonization can be available to a fuel for a steam generation boiler. The exhaust heat from the boiler is used sequentially for drying of sludge. The active cokes are applied to the adsorbent for dioxin removal in exhaust gas from incinerators of wastes, or for purification of gas obtained in a gasification process of wastes, particularly removal of H2S. The used adsorbent is not recycled, but incinerated in the furnace without a desorption process to decompose adsorbed dioxin or to oxidize H2S for a sequential desulfurization process of SO2. Dry pellets of sludge were carbonized in a quartz tube reactor under various atmospheres. The micro pore structure and the adsorption performance of the cokes produced without activation process were examined. The micro pore structure was influenced by the temperature, the sort of flow gas (N2, CO2 and steam) and carbonization time, and the active cokes produced under the condition of the temperature 823 K for 60 min in the steam atmosphere had a largest specific surface area in the diameter less than 5 nm. The amount of benzene adsorption as an alternative substance of dioxin into the active cokes had a similar quality to a commercial active char produced from coal if it was evaluated by adsorption per a unit specific surface area. This fundamental knowledge must be reflected to an optimum design for development of a simple continuous process to produce the active cokes by a fluidized bed type of the carbonization furnace.     

Bio-oil production by fast pyrolysis of cellulose/polyethylene mixtures in the presence of metal chloride

Cellulose/polyethylene mixture (3:1 w/w) and Tetra Pak wastes with and without metal chloride (ZnCl₂, AlCl₃, CuCl₂, FeCl₃) addition were subjected to a fast pyrolysis process at 350–500 °C and heating rate 100 °C/s to evaluate the possibility of liquid product formation with a high yield. The addition of zinc, aluminum, iron and copper chlorides has influenced the range of samples decomposition as well as the chemical composition of resulting pyrolytic oils. It was found that formation of levoglucosan, the main product of cellulose thermal decomposition, and phenol and its derivatives decreased in a presence of metal chlorides. Non-catalytic fast pyrolysis of polyethylene leads to the formation of solid long chain hydrocarbons, whereas the addition of metal chlorides promotes the formation of more liquid hydrocarbons.     

An assessment of municipal solid waste compost quality produced in different cities of India in the perspective of developing quality control indices

A study was conducted to investigate physico-chemical properties, fertilizing potential and heavy metal polluting potentials of municipal solid waste composts produced in 29 cities of the country. Results indicated that except a very few samples, all other samples have normal pH and EC. Organic matter as well as major nutrients N and P contents in MSW composts are generally low as compared to the composts prepared from rural wastes. Heavy metal contents in composts from bigger cities (>1 million population) were higher by about 86% for Zn, 155% for Cu, 194% for Cd, 105% for Pb, 43% for Ni and 132% for Cr as compared to those from smaller cities (<1 million population). Composts prepared from source separated biogenos wastes contained, on average, higher organic matter (by 57%), total N (by 77%) and total P (by 78%), but lower concentrations of heavy metals Zn (by 63%), Cu (by 78%), Cd (by 64%), Pb (by 84%), Ni (by 50%), and Cr (by 63%) as compared to those prepared from mixed wastes. Partial segregation at the site of composting did not improve quality of compost significantly in terms of fertilizing parameters and heavy metal contents. Majority of MSW composts did not conform to the quality control guideline of ‘The Fertilizer (Control) Order 1985’ in respect of total organic C, total P, total K as well as heavy metals Cu, Pb and Cr. In order to enable the relevant stakeholders to judge overall quality, a scheme has been proposed for the categorization of composts into different marketable classes (A, B, C, and D) and restricted use classes (RU-1, RU-2, and RU-3) on the basis their fertilizing potential and as well as potential for contaminating soil and food chain. Under the scheme, ‘Fertilizing index’ was calculated from the values of total organic C, N, P, K, C/N ratio and stability parameter, and ‘Clean index’ was calculated from the contents of heavy metals, taking the relative importance of each of the parameters into consideration. As per the scheme, majority of the compost samples did not belong to any classes and hence, have been found unsuitable for any kind of use. As per the regulatory limits of different countries, very few compost samples (prepared from source separated biogenos wastes) were found in marketable classes (A, B, C and D) and some samples (11–14) were found suitable only for some restricted use.     

Waste collection systems for recyclables: An environmental and economic assessment for the municipality of Aarhus (Denmark)

Recycling of paper and glass from household waste is an integrated part of waste management in Denmark, however, increased recycling is a legislative target. The questions are: how much more can the recycling rate be increased through improvements of collection schemes when organisational and technical limitations are respected, and what will the environmental and economic consequences be? This was investigated in a case study of a municipal waste management system. Five scenarios with alternative collection systems for recyclables (paper, glass, metal and plastic packaging) were assessed by means of a life cycle assessment and an assessment of the municipality’s costs. Kerbside collection would provide the highest recycling rate, 31% compared to 25% in the baseline scenario, but bring schemes with drop-off containers would also be a reasonable solution. Collection of recyclables at recycling centres was not recommendable because the recycling rate would decrease to 20%. In general, the results showed that enhancing recycling and avoiding incineration was recommendable because the environmental performance was improved in several impact categories. The municipal costs for collection and treatment of waste were reduced with increasing recycling, mainly because the high cost for incineration was avoided. However, solutions for mitigation of air pollution caused by increased collection and transport should be sought.     

Insight into the Adsorption Properties of Chitosan/Zeolite-A Hybrid Structure for Effective Decontamination of Toxic Cd (II) and As (V) Ions from the Aqueous Environments

Chitosan/zeolite-A hybrid structure (CS/Z.A) was synthesized and characterized as a multifunctional and environmental adsorbent for the Cd (II) and As (V) ions. The adsorption capacities of CS/ZA for Cd (II) and AS (V) are 170 mg/g and 125 mg/g, respectively which are higher values than several adsorbents in literature. The kinetic study demonstrates Pseudo-First-order behavior for the Cd (II) adsorption process and Pseudo-second order for the As (V) uptake reactions. The Cd (II) and As (V) uptake reactions follow the Freundlich equilibrium behavior with heterogeneous and multilayer adsorption properties. The kinetic and equilibrium studies in addition to the Gaussian energy {6.35 kJ/mol [Cd (II)] and 9.44 kJ/mol [As (V)]} demonstrate physical properties for the Cd (II) adsorption mechanism and more chemical behavior for the As (V) adsorption mechanism. The thermodynamic study declares exothermic, spontaneous, and favorable adsorption reactions for Cd (II) and As (V) by CS/Z.A composite. The CS/Z.A is of significant capacity for Cd (II) and As (V) ions in the existence of other competitive dissolved anions (PO₄^3?, NO₃^?, and SO₄^2?) and other metals [Zn (II), Co (II), and Pb (II)]. Finally, the CS/Z.A composite is a recyclable product and can be applied in effective Cd (II) and As (V) decontamination processes for five runs.

     

Evaluation of environmental impacts of food waste management by material flow analysis (MFA) and life cycle assessment (LCA)

This paper focuses on the evaluation of potential environmental impacts of food waste management practices by material flow analysis (MFA) and life cycle assessment (LCA) during different life cycle stages toward the environmentally sustainable options for Daejeon Metropolitan City (DMC) in Korea. The MFA and LCA studies were conducted to examine different recycling facilities of food waste. The results of the LCA study indicate that, among the different recycling methodologies currently in practice in DMC, Scenario 4 (wet and dry feed site) conduced to higher global warming potential (GWP) and higher acidification potential (AP), whereas Scenarios 2 (wet feed site 1) and 3 (wet feed site 2) resulted in the lowest impact. This is mainly due to the emission caused during the treatment stage. For eutrophication potential (EP), Scenario 1 (composting site) contributed to higher environmental impacts due to the emission of ammonia generated during the treatment process, while in case of photochemical ozone creation potential (POCP), the collection stage for all recycling facilities led to higher impacts to the environment due to the combustion of fossil fuels. This study indicates that the proper disposal of the final residues, such as solid sludge and screened materials, could aid in reducing environmental burdens.     

Electrochemical reduction of Cr(VI) in the decontamination process ELDECON

One of ABB Atom's methods, ELDECON, is an electrochemical process for decontamination of components used in nuclear power plants. ELDECON removes radioactive species while producing small amounts of waste. However, the waste sludge that is produced in the ELDECON process contains chrornate (Cr(VI)). According to the US Cod of Feguration, 40 CFR 261, if a process in any step creates chromate, the final waste has to be tested in a toxicity characteristic leachate procedure. In order to pass the test, the chromate has to be reduced to chromium (Cr(III)). Electrochemistry has proven to be a valuable tool. When incorporating indirect electrolysis into the ELDECON concept, the chromate ions are reduced. This is done by the use of an electrochemical cell (reactor bed). The method involves ferric nitrate as a reagent which, besides converting the chromate completely, also decreases the reaction time. The reaction time and the amount of solution treated in the cell have a close to linear relationship (i.e. the reaction time is proportional to the amount of solution). This makes the test cell feasible to scale up and use in the industry.     

A performance history of the base catalyzed decomposition (BCD) process

Remediation of halogenated organic compounds—such as polychlorinated biphenyls (PCBs), polychlorinated dibenzo-p-dioxins (PCDDs), and polychlorinated dibenzofurans (PCDFs)—poses a challenge because these compounds are resistant to microbial attack and to degradation by many common chemicals. Since the mid-1980s, the Environmental Protection Agency's (EPA's) Office of Research and Development in Cincinnati, Ohio—the National Risk Management Research Laboratory (NRMRL)—has funded research and development efforts to develop specialized, chemical dehalogenation processes for detoxifying PCBs and related compounds. NRMRL owns domestic rights for “basic process” patents on a chemical dehalogenation process commonly known as Base Catalyzed Decomposition (BCD). EPA has licensed the process to two firms for use in the United States. This article summarizes laboratory-scale, pilot-scale, and field performance data on BCD technology collected to date by various governmental, academic, and private organizations.     

Estimation on Biodegradability of Poly (3-hydroxybutyrate-<Emphasis Type="Italic">co</Emphasis>-3-hydroxyvalerate) (PHB/V) and Numbers of Aerobic PHB/V Degrading Microorganisms in Different Natural Environments

To assess the capacity of the natural environment for degrading PHB/V, the film-MPN method proposed previously was modified to estimate the numbers of PHB/V degrading microorganisms (degraders) in various environments. The First-Order Reaction (FOR) model was used to determine the appropriate incubation period for the method. Numbers of aerobic PHB/V degraders were estimated in garden soil, paddy field soil, farm soil, river bank soil, infertile garden soil, river water, activated sludge, and seawater by the film-MPN method. Results were compared with those estimated by the clear-zone technique and showed that the film-MPN method was suitable for estimating the numbers of PHB/V degraders in the environments tested. On the other hand, biodegradability of injection molded PHB/V samples was investigated in several kinds of environments. The changes of weight were studied and results showed that biodegradability of PHB/V related to the numbers of PHB/V degraders in similar ecosystem in different regions. In different environments the biodegradability of PHB/V not only related to the number of PHB/V degraders, but also depended on whether there were conditions for the PHB/V degraders to grow and proliferate easily in the environment.     

Removal of Oil from Oil-in-Water Emulsion by Poly (Sulfur/Soya Bean Oil) Composite Adsorbent: An Equilibrium Study

Journal of Polymers and the Environment - This work describes synthesis of poly (sulfur/soya bean oil) composite material by co-polymerization of elemental sulfur and soya bean oil at...     

Toxicity of the weathered crude oil used at the Newfoundland offshore burn experiment (NOBE) and the resultant burn residue

The toxicity of the weathered crude oil Alberta sweet mixed blend (ASMB) used at the Newfoundland offshore burn experiment (NOBE) and the resultant burn residue, was investigated using the Environment Canada water-accommodated fraction (WAF) preparation method and exposure protocol. Rainbow trout (Oncorhynchus mykiss) were exposed to freshwater WAF prepared from weathered ASMB. Three-spine stickleback (Gasterosteus aculeatus), and the gametes of the white sea urchin (Lytechinus pictus) were exposed to saltwater WAF prepared from both weathered ASMB and burn residue. The fish tests were of 96 h duration, and the end-point was lethality. The urchin test was of 20 min duration, and the end-point was inhibition of fertilization. GC/MS headspace analysis of 28 analytes showed low levels of volatile hydrocarbons. The maximum measured concentration was 1.1 μg ml⁻¹ in 104 samples from all WAF concentrations in both seawater and freshwater at all exposure times (0, 24 and 72 h). All samples were found not to be toxic to all species tested.