Controlled sintering for cadmium stabilization by beneficially using the dredged river sediment

● Dredged river sediment was proved as a ceramic precursor rather than a solid waste. ● Cd was stabilized in Cd-Al-Si-O phases at low temperatures via sediment addition. ● < 5% of Cd was leached out from sintered products even after a prolonged time. ● A strategy was proposed to simultaneously reuse wastes and stabilize heavy metals. Cd-bearing solid wastes are considered to be a serious threat to the environment, and effective strategies for their treatment are urgently needed. Ceramic sintering has been considered as a promising method for efficiently incorporating heavy metal-containing solid wastes into various ceramic products. Mineral-rich dredged river sediment, especially Al and Si-containing oxides, can be treated as alternative ceramic precursors rather than being disposed of as solid wastes. To examine the feasibility of using waste sediment for Cd stabilization and the phase transition mechanisms, this study conducted a sintering scheme for the mixtures of CdO and dredged river sediment with different (Al+Si):Cd mole ratios. Detailed investigations have been performed on phases transformation, Cd incorporation mechanisms, elemental distribution, and leaching behaviors of the sintered products. Results showed that Cd incorporation and transformation in the sintered products were influenced by the mole ratio of (Al+Si):Cd. Among the high-Cd series ((Al+Si):Cd = 6:1), CdSiO₃, Cd₂SiO₄, CdAl₂(SiO₄)₂ and Cd₂Al₂Si₂O₉ were predominant Cd-containing product phases, while Cd₂Al₂Si₂O₉ was replaced by CdAl₄O₇ when the mole ratio of (Al+Si):Cd was 12:1 (low-Cd series). Cd was efficiently stabilized in both reaction series after being sintered at ≥ 900 °C, with < 5% leached ratio even after a prolonged leaching time, indicating excellent long-term Cd stabilization. This study demonstrated that both Cd-containing phases and the amorphous Al-/Si-containing matrices all played critical roles in Cd stabilization. A promising strategy can be proposed to simultaneously reuse the solid waste as ceramic precursors and stabilize heavy metals in the ceramic products.     

Particle size distributions and health-related exposures of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) of sinter plant workers

This study measured particle size distributions of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) in two workplace atmospheres of the sintering grate and rough roll shredder in a sintering plant, and to assess their workers’ health-related exposures. We found that the PCDD/F concentration of the sintering grate (site A = 14.47 pg m⁻³) was lower than that of the rough roll shredder (site B = 17.20 pg m⁻³). Particle size distributions of PCDD/Fs were in the form of the unimodal with the mass median aerodynamic diameter (MMAD) of 4.74 μm and 5.23 μm, and geometric standard deviation (σ_g) of 3.15 and 2.15 for the site A and B, respectively. The above results suggest that the workplace of the site A had a less fraction of coarse particles than that of the site B. The estimated PCDD/F concentrations of the inhalable fraction (11.0 pg m⁻³) and thoracic fraction (8.89 pg m⁻³) of the site A were lower than those of the site B (12.4 and 9.39 pg m⁻³, respectively). But to the contrary the estimated respirable fraction of the site A (5.05 pg m⁻³) was slightly higher than that of the site B (4.93 pg m⁻³). Our results clearly indicate the importance to conduct particle size segregating samplings for assessing human PCDD/F exposures.     

Air emissions of ammonia and methane from livestock operations: valuation and policy options

The animal husbandry industry is a major emitter of ammonia (NH3), which is a precursor of fine particulate matter (PM2.5)--arguably, the number-one environment-related public health threat facing the nation. The industry is also a major emitter of methane (CH4), which is an important greenhouse gas (GHG). We present an integrated process model of the engineering economics of technologies to reduce NH3 and CH4 emissions at dairy operations in California. Three policy options are explored: PM offset credits for NH3 control, GHG offset credits for CH4 control, and expanded net metering policies to provide revenue for the sale of electricity generated from captured methane (CH4) gas. Individually these policies vary substantially in the economic incentives they provide for farm operators to reduce emissions. We report on initial steps to fully develop the integrated process model that will provide guidance for policy-makers.     

Optimization of Reburning for Advanced N0x Control on Coal-fired Boilers

This paper summarizes an experimental study which was conducted to investigate the chemical constraints of the reburning process and identify reburning configurations for optimal NO_x reduction in coal-fired boilers. Tests were performed on a bench scale tunnel furnace to characterize and optimize the fuel-rich reburning zone and the fuel-lean burnout zone independently. Detailed measurements ofunburned hydrocarbons, CO, NH₃, and HCN were made at the reburning zone exit. The influence of the concentrations of reactive species was examined as were temperature effects for both the reburning and burnout zone. Results indicated that reburning zone chemistry was not rate limiting. The impacts of temperature and burnout zone oxidation were of major importance. Integration of the optimum reburning and burnout zone configurations resulted in increased NO_x reduction. Over 85 percent reduction in NO_x emissions was achieved with ammonium sulfate injection in the burnout zone under optimum reburning conditions.     

Effect of crystal size on zinc stabilization in aluminum-rich ceramic matrix

With aluminum as the predominant element, incineration residues from municipal solid waste and sewage sludge may be reused as precursors for zinc stabilization. As solid-state reactions are influenced by the crystal sizes of the reactants, the aluminum-containing components with different crystal sizes in the incineration residues may affect zinc transformation and immobilization. In this study, Al₂O₃ was prepared with a variety of crystal sizes to simulate the aluminum-rich incineration residue matrix, and ZnO was mixed with Al₂O₃ to study the zinc incorporation mechanisms. The crystal sizes of Al₂O₃ were determined using Rietveld refinement. Quantification results showed that ~?30% of zinc was incorporated into the ZnAl₂O₄ spinel when Al₂O₃ with the largest crystal size was used. However, the zinc transformation was enhanced twofold when the Al₂O₃ precursor had the smallest crystal size. This study confirmed the potential enhancement of zinc immobilization by nanoscale crystals in simulated aluminum-rich incineration residues. By improving zinc stabilization efficiencies using poorly crystallized aluminum-containing compounds instead of increasing the energy consumption by increasing the sintering temperatures, we can achieve an economic and environmental win–win scenario for the beneficial utilization of incineration residues of municipal solid waste and sewage sludge.     

Economic and health benefits of the co-reduction of air pollutants and greenhouse gases

This study examines the monetary value of social costs—private costs and negative externalities—that could be avoided by energy conservation actions. A novel Air Resource Co-Benefits (ARCoB) model has been developed in this study to assess the comprehensive social benefits of greenhouse gas GHG mitigation policy. The rollback model is used to estimate changes in air pollutant concentrations attributed to the emission reductions. Change in ozone concentration is converted from non-methane hydrocarbons based on the maximum ozone increment reactivity. In addition to saved medical expenditure, years of potential life lost (YPLL) is estimated based on the exposure-response coefficients for mortality and is calculated with abridged life table. Two cases of energy efficiency improvement in different scales are analyzed to estimate the annual co-benefits of abatements of air pollutants and greenhouse gas in 2009: 1) the energy intensity reduction in the industrial sector and 2) energy saving at Taipei Taiwan City Hall. Results indicate the saved energy cost accounted for 66 % and 70 % in the first and second case, respectively, and was a major part of the total benefit from energy conservation. The saved air pollution fee was 7.8–8.5 times lower than the averted health cost of medical expenditure, which was US$10.34 million in the first case, in which there were also averted YPLL of 3,478 person-years or averted deaths of 311 persons per year.     

Jobs Versus the Environment: An Industry-Level Perspective

The possibility that workers could be adversely affected by increasingly stringent environmental policies has led to claims of a “jobs versus the environment” trade-off by both business and labor leaders. The present research examines this claim at the industry level for four heavily polluting industries: pulp and paper mills, plastic manufacturers, petroleum refiners, and iron and steel mills. Combining a unique plant-level data set with industry-level demand information, we find that increased environmental spending generally does not cause a significant change in employment. Our average across all four industries is a net gain of 1.5 jobs per $1 million in additional environmental spending, with a standard error of 2.2 jobs—an economically and statistically insignificant effect. There are statistically significant and positive effects in two industries, but total number of affected jobs remains quite small. These small positive effects can be linked to labor-using factor shifts and relatively inelastic estimated demand.     

Removing nitric oxide from flue gas using iron(II) citrate chelate absorption with microbial regeneration

The addition of metal chelates such as Fe(II)EDTA or Fe(II)Cit to wet flue gas desulfurization systems has been shown to increase the amount of NO(x) absorption from gas streams containing SO(2). This paper attempts to demonstrate the advantage of not only using Fe(II)Cit chelate to absorb nitrogen oxides from flue gas but also the advantage gained from adding microorganisms to the system. Two distinct classes of microorganisms are needed: denitrifying and iron-reducing bacteria. The presence of oxygen in flue gas will affect the absorption efficiency of NO by Fe(II)Cit chelate. The oxidation of Fe(II) can be slowed with the help of bacteria in two ways: bacteria can serve to directly reduce Fe(III) to Fe(II) or they can serve to keep levels of dissolved oxygen in the solution low. As a result, after NO absorption, Fe(II)(Cit)NO will be reduced by denitrifying bacteria to Fe(II)Cit while Fe(III) is reduced by anaerobic bacteria back to Fe(II). Our experiments have shown that the implementation of our protocol allowed for an NO reduction rate constant increase from standard levels of 0.0222-0.100 m Mh(-1) with inlet NO changed from 250 to 1000 ppm. We have also found that total Fe concentration tends to decrease after prolonged periods of operation due to the loss of some Fe to the formation of Fe(OH)(3) that settles together with the sludge at the bottom of bioreactor tank.     

Using a Mass Balance Model to Evaluate Groundwater Budget of Seawater‐Intruded Island Aquifers1

Jang, Cheng‐Shin, Chen‐Wuing Liu, Shih‐Kai Chen, and Wen‐Sheng Lin, 2011. Using a Mass Balance Model to Evaluate Groundwater Budget of Seawater‐Intruded Island Aquifers. Journal of the American Water Resources Association (JAWRA) 48(1): 61‐73. DOI: 10.1111/j.1752‐1688.2011.00593.x Abstract: The study developed a mass balance model to evaluate the groundwater budget of seawater‐intruded island aquifers using limited available data. The Penghu islands were selected as a study area. As sparse observed data were available in the islands, methods of combining water and chloride balances were used to determine the amounts of groundwater pumping, seawater intrusion, aquifer storages, and safe yields in the shallow and deep aquifers. The groundwater budget shows that seawater intrusion to freshwater aquifers was 1.38 × 10⁶ and 0.29 × 10⁶ m³/year in the shallow and deep aquifers, respectively, indicating that the seawater intrusion is severe in the both aquifers. The safe yield of the shallow aquifer was 14.56 × 10⁶ m³/year in 2005 which was four times higher than that of the deep aquifer (3.70 × 10⁶ m³/year). However, the annual pumping amounts in the shallow and deep aquifers were 4.77 × 10⁶ and 3.63 × 10⁶ m³/year, respectively. Although the safe yield of the shallow aquifer is enough for all water resources demands, only 55% of exploitation amount was extracted from the shallow aquifer due to its poor water quality. Groundwater exploitation in the deep aquifer should be significantly reduced and regulated by a dynamic management of pumping scheme because the annual pumping amounts are close to the safe yield and seawater intrusion occurs continually. Additionally, to alleviate further aquifer salination, at least half of the current annual groundwater abstraction should be reduced.     

Metal stabilization mechanism of incorporating lead-bearing sludge in kaolinite-based ceramics

The feasibility and mechanism of incorporating simulated lead-laden sludge into low-cost ceramic products was investigated by observing the reaction of lead with two kaolinite-based precursors under sintering conditions. To investigate the phase transformation process of lead, lead oxide (PbO) mixed with a kaolinite or mullite precursor were fired at 500-950 °C for 3 h. Detailed X-ray diffraction analysis of sintered products revealed that both precursors had crystallochemically incorporated lead into the lead feldspar (PbAl₂Si₂O₈) crystalline structure. By mixing lead oxide with kaolinite, lead feldspar begins to crystallize at 700 °C; maximum incorporation of lead into this structure occurred at 950 °C. However, two intermediate phases, Pb₄Al₄Si₃O₁₆ and a polymorph of lead feldspar, were detected at temperatures between 700 and 900 °C. By sintering lead oxide with the mullite precursor, lead feldspar was detected at temperatures above 750 °C, and an intermediate phase of Pb₄Al₄Si₃O₁₆ was observed in the temperature range of 750-900 °C. This study compared the lead leachabilities of PbO and lead feldspar using a prolonged leaching test (at pH 2.9 for 23 d) modified from the toxicity characteristic leaching procedure. The results indicate the superiority of lead feldspar in stabilizing lead and suggest a promising and reliable strategy to stabilize lead in ceramic products.