Current status and perspectives of accelerated carbonation processes on municipal waste combustion residues

The increasing volumes of municipal solid waste produced worldwide are encouraging the development of processes to reduce the environmental impact of this waste stream. Combustion technology can facilitate volume reduction of up to 90%, with the inorganic contaminants being captured in furnace bottom ash, and fly ash/APC residues. The disposal or reuse of these residues is however governed by the potential release of constituent contaminants into the environment. Accelerated carbonation has been shown to have a potential for improving the chemical stability and leaching behaviour of both bottom ash and fly ash/APC residues. However, the efficacy of carbonation depends on whether the method of gas application is direct or indirect. Also important are the mineralogy, chemistry and physical properties of the fresh ash, the carbonation reaction conditions such as temperature, contact time, CO₂ partial pressure and relative humidity. This paper reviews the main issues pertaining to the application of accelerated carbonation to municipal waste combustion residues to elucidate the potential benefits on the stabilization of such residues and for reducing CO₂ emissions. In particular, the modification of ash properties that occur upon carbonation and the CO₂ sequestration potential possible under different conditions are discussed. Although accelerated carbonation is a developing technology, it could be introduced in new incinerator facilities as a “finishing step” for both ash treatment and reduction of CO₂ emissions.     

Mineralization and Transfer Processes of <Superscript>14</Superscript>C-labeled Pesticides in Outdoor Lysimeters

A recently designed two-chamber-lysimeter-test-system allows the detailed investigation of degradation, transport and transfer processes of ¹⁴C-labeled substances in soil–plant–atmosphere-systems under outdoor conditions. With this test system it is feasible to distinguish between ¹⁴C-emissions from soil surfaces and ¹⁴C-emissions from plant surfaces in soil monoliths under real environmental conditions. Special soil humidity sensors allow the measurement of soil water content near to the soil surface, in 1 and 5 cm depth. The behavior of organic chemicals can be followed for a whole vegetation period and a mass balance for the applied chemical can be established. Some selected results of the herbicides isoproturon and glyphosate – using the two-chamber-lysimeter-test-system – are presented to demonstrate its applicability for the identification and quantification of the processes that govern pesticide behavior in soil–plant-systems. Mineralization of ¹⁴C-isoproturon was very different in four different soils; the mineralization capacity of the soils ranged from 2 to 60%. Leaching of isoproturon in general was very low, but depending on the soil type and environmental conditions isoproturon and its metabolites could be leached via preferential flow, especially shortly after application. For the herbicide ¹⁴C-glyphosate no accumulation of residues in the soil and no leaching of the residues to deeper soil layers could be observed after three applications. Glyphosate was rapidly degraded to AMPA in the soil. Glyphosate and AMPA were accumulated in soy bean nodules.     

Evaluation of the use of a sequential extraction procedure for the characterization and treatment of metal containing solid waste

Metal containing wastes like MSWI fly ashes and blast furnace sludge form a major environmental problem as they are polluted with heavy metals. The ash has to be landfilled or can be used as a construction material, but a pretreatment is in general necessary. Washing of the ashes with water in order to dissolve soluble salts or extracting the heavy metals with chemicals are possibilities. Blast furnace sludge contains large quantities of iron and carbon and could be recycled in the blast furnace, if the zinc content were not that high. Using a hydrometallurgical process the zinc can be removed from the sludge particles. In order to evaluate such treatment methods knowledge of the leaching behaviour of the studied material is very important. One of the factors influencing the leaching behaviour is the composition and mineralogy of the solids. A sequential extraction procedure, whereby the material is sequentially leached with different leaching solutions, can be used as an aid to characterize the material and to determine which chemical conditions are needed to obtain a sufficient extraction efficiency. To verify the accuracy of the sequential extraction procedure, a method is tested on MSWI fly ash and evaluated by comparing the results with those of leaching experiments whereby the final pH of the leaching solutions is varied over a wide range. Based upon this evaluation some suggestions for the use of the sequential extraction procedure are made and an adapted procedure is suggested, and applied to a blast furnace sludge.     

Effect of fertilization and irrigation schedule on water and fertilizer solute transport for wheat crop in a sub-humid sub-tropical region

In order to increase the water and fertilizer use efficiency and decrease the losses of water and fertilizer solutes (N and P), it is necessary to assess the influence of level of fertilization and irrigation schedule on movement and balance of water and fertilizers in the root zone. With this goal, the reported study was undertaken to determine the effect of fertilization and irrigation schedule on water movement and fertilizer solute transport in wheat crop field in a sub-tropical sub-humid region. Field experiments were conducted on wheat crop of cultivar Sonalika (Triticum aestivum L.) during the years 2002–2003, 2003–2004 and 2004–2005. Each experiment consisted of four fertilizer treatments and three irrigation treatments during the wheat growth period. During the experiment, the irrigation treatments were: I₁ = 10% maximum allowable depletion (MAD) of available soil water (ASW); I₂ = 40% MAD of ASW; I₃ = 60% MAD of ASW. The fertilizer treatments during the experiment were: F₁ = control treatment with N:P₂O₅:K₂O as 0:0:0 kg ha⁻¹; F₂ = fertilizer application of N:P₂O₅:K₂O as 80:40:40 kg ha⁻¹; F₃ = fertilizer application of N:P₂O₅:K₂O as 120:60:60 kg ha⁻¹ and F₄ = fertilizer application of N:P₂O₅:K₂O as 160:80:80 kg ha⁻¹. The results of the investigation revealed that low volume high frequency irrigation results in higher deep percolation losses than the low frequency high volume irrigation with different levels of fertilization for wheat crop in coarse lateritic soil, whereas different levels of fertilization did not significantly affect soil water balance of the wheat crop root zone during all the irrigation schedules. Level of fertilization and irrigation schedule had significant effect on nitrogen leaching loss whereas irrigation schedules had no significant effect on nitrogen uptake under different levels of fertilization. On the other hand, the leaching loss of phosphorus was not significantly influenced by the irrigation schedule and level of fertilization of wheat crop. This indicated that PO₄–P leaching loss was very low in the soil solution as compared to nitrogen due to fixation of phosphorus in soils. From the observed data of nitrogen and phosphorus use efficiency, it was revealed that irrigation schedule with 40% maximum allowable depletion of available soil water with F₂ fertilizer treatment (N:P₂O₅:K₂O as 80:40:40 kg ha⁻¹) was the threshold limit for wheat crop with respect to nitrogen and phosphorus use, crop yield and environmental pollution.     

Importance of indirect nitrous oxide emissions at the field, farm and catchment scale

Direct and indirect nitrous oxide (N₂O) emissions and leaching losses from an intensively managed grazed pasture in the Ythan catchment, Aberdeenshire, UK, were measured and compared over a 17-month period. Simultaneous measurements of farm-wide leaching losses of N₂O were also made and catchment-wide fluxes were estimated from existing N leaching data. The relative importance of direct and indirect N₂O fluxes at the field, farm and catchment scale was then assessed. At the field scale we found that direct N₂O emissions were low (1.2 kg N ha⁻¹ year⁻¹, 0.6% of N input) with indirect N₂O emissions via drainage waters comprising a significant proportion (25%) of total N₂O emissions. At the whole-farm scale, the N₂O-N emission factor (0.003) for leached NO₃-N (EF_5-g) was in line with the IPCC's recent downward revision. At the catchment scale, a direct N₂O flux of 1.9 kg N ha⁻¹ year⁻¹ and an indirect flux of 0.06 kg N₂O-N ha⁻¹ year⁻¹ were estimated. This study lends further support to the recent downward revision of the IPCC emission factor for N₂O arising from leached N in surface and ground waters (EF_5-g) and highlights the need for multiple point sampling to ensure that the importance of indirect N₂O losses via drainage waters is not misrepresented at the farm and catchment scales.     

An overview for the utilization of wastes from stainless steel industries

Significant quantities of wastes are generated as the waste materials or byproducts every day from stainless steel processes. According to the origins and characteristics, the stainless steel wastes can be mainly classified into two categories, slags and dusts. They usually contained considerable quantities of valuable metals and materials. This paper summarized and analyzed the generation, composition, characteristics and the leaching behaviors of the most of wastes obtained from the stainless steel processes. On this basis, a review of several methods for treating the various stainless steel wastes was made. It is very essential not only for recycling the valuable metals and mineral resources but also for protecting the environment.     

磷在原状土中的淋溶规律

研究磷在原状土中的淋溶规律及不同因素的影响。采用自行设计的原状土淋溶柱,探讨了磷在原状土中的淋溶规律。分别用pH值为4.0、6.8和9.0的淋溶液淋溶原状土,当淋溶液p H值由9.0降至6.8时,磷的总淋出量由2120.mg升至238.1 mg,增幅较小,p H值继续降至4.0,磷的总淋出量增加至271.9 mg;与未酸化的土壤相比,酸化后土壤中,磷的淋出量增加了22.18%,说明土壤酸化会增加磷的流失;以4 d为一个冻融周期,进行了不同冻融频次和冻前含水率的交替冻融试验。结果表明:在冻融频次小于5次时,磷的淋失量与冻融频次呈正相关,当冻融频次大于5次时,磷的淋出量随冻融频次的增加而减小;土壤冻前含水率越大,磷的淋失量也越大,冻前含水率由15%增加到25%时,淋失量由217.3 mg增长到316.2 mg,增长了45.50%。     

燃煤飞灰中汞在渗滤过程中的迁移规律研究

燃煤飞灰在堆放、填埋过程中,固定于灰中的汞可能被再次释放,而带来二次污染。为研究飞灰中汞对环境的影响,本研究参照国标规定的渗滤方法和美国毒性特征浸出程序,对飞灰中汞的渗滤特性进行研究,即研究不同类型酸浸取液、浸取液pH值以及液固比对汞渗滤特性的影响。不同酸的浸取试验结果表明：硝酸的汞渗出浓度最大,硫酸最小,经化学动力学分析是由于不同类型酸对于玻璃体中各种氧化物溶解能力的差异性所致。采用硫酸渗滤时,出现反常的渗滤特征,并发现该现象与飞灰二次相生成物有关。滤液汞浓度随浸取液pH的增大成指数曲线下降趋势;随液固比增加,滤液汞浓度呈单峰分布,经化学动力学分析表明氢离子与硅铝玻璃体的配比是产生这一现象的主要原因;本研究对于燃煤汞污染的深度控制及治理方面有指导意义。     

Evaluation of leaching characteristic and kinetic study of lithium from lithium aluminum silicate glass-ceramics by NaOH

The behavior and mechanism of Li leaching from lithium aluminum silicate glass-ceramics which can be used as a secondary source of Li using aqueous NaOH solution was investigated. The Li leaching efficiency is increased with increasing concentration of NaOH, specific surface area, and reaction temperature. When leached under optimum conditions, 2 mol/L NaOH, 53 μm particle undersize, 1:10 solid/liquid ratio, 250 r/min stirring speed, 100°C reaction temperature, 12 hr, the Li leaching efficiency was approximately 70%. However, when the leaching experiment was performed for 48 hr, the concentration of Li⁺ ions contained in the leach liquor decreased from 1160 to 236 mg/L. To investigate the origin of this phenomenon, the obtained leach residue was analyzed by X-ray diffraction, scanning electron microscopy, and energy-dispersive X-ray spectroscopy. These analyses show that zeolite was formed around the lithium aluminum silicate glass-ceramics, which affected the leaching of by adsorbing Li⁺ ions. In addition, using the shrinking-core model and the Arrhenius equation, the leaching reaction with NaOH was found to depends on the chemical reaction of the two reactants, with a higher than 41.84 kJ/mol of the activation energy.     

黄浦江上游蔬菜田氮素流失规律测坑研究

通过测坑试验,研究了黄浦江上游蔬菜田渗漏水中氮素的变化动态和流失规律。结果表明,蔬菜田渗漏水中氮素以NO3^--N为主,NO3^--N作为氮素在土壤中流失的主要形态将成为施用氮肥造成地下水污染的重要来源;施用精制有机肥或粗猪粪代替部分化学氮肥有利于减少蔬菜田渗漏水中氮素的流失。