垃圾焚烧飞灰重金属含量与渗滤特性分析

对国内 2种不同的垃圾焚烧炉型———炉排炉与流化床产生的飞灰进行了特性分析 .结果表明 ,飞灰在粒径分布上有相似的规律 .炉排炉飞灰中重金属含量高于流化床飞灰中的含量 .飞灰的渗滤特性表明 ,重金属的渗滤特性受渗滤液的pH影响很大 .     

粉煤灰吸附去除弱酸性艳蓝印染废水

利用粉煤灰对弱酸性艳蓝印染废水进行了处理。研究表明：粉煤灰的粒径、灰水比、废水pH值以及振荡吸附时间对粉煤灰的吸附能力均有较大影响。在以下工艺条件下：20℃,粉煤灰的粒径200目,灰水比为1：30,pH为2．0,振荡吸附2．5h,弱酸性艳蓝印染废水经粉煤灰处理后,COD值由576mg／L降至71mg／L,COD去除率可达87．7％：废水色度可从10000倍降为50倍,色度的去除率达99．5％,出水pH为6．5。出水水质达到了国家印染废水一级排放标准(GB4287—92)。     

利用粉煤灰固化含砷污泥的研究

对于As浸出率超标的硫酸废水处理系统污泥,应用固化处理可以有效降低砷浸出率。文章用水泥及粉煤灰固化冶炼厂硫酸废水中和污泥,以As的浸出率为控制指标,从时间、物料配比、pH值等方面考虑对固化块浸出率的影响,寻找粉煤灰最佳掺入量,有效降低处理成本,并尽量减少固体废物对环境的有害影响。与水泥固化相对比,采用粉煤灰固化具有更好的固化效果和明显经济效益。     

螯合型表面活性剂对垃圾焚烧飞灰改性的研究

以垃圾焚烧飞灰的高附加值资源化和稳定化为目标,研究了螯合型表面活性剂对垃圾焚烧飞灰改性活化和对重金属的稳定螯合效果.通过活化指数和红外光谱分析,在改性剂用量7.0mL/100g飞灰、改性时间15min和改性温度75℃的条件下,ACS1改性飞灰的活化指数可达95%以上.美国环保局固体废弃物浸出毒性试验表明,螯合型表面活性剂对飞灰中重金属具有较强的束缚能力.     

工业燃煤锅炉烟气循环方式下飞灰的汞吸附特性

为探究燃煤锅炉烟气循环方式下飞灰汞的吸附特性,利用固定床汞吸附装置,对立式煤粉沉降炉不同模拟烟气循环工况条件下形成的飞灰汞吸附特性进行了研究,重点考察了烟气循环比例、煤种、关键燃烧气体组分等因素的影响.结果表明:①烟气循环工况条件下形成的飞灰汞吸附能力明显优于非烟气循环工况（空气燃烧）条件下形成的飞灰,并且随烟气循环比例的增加,飞灰汞吸附量呈逐渐增加趋势.褐煤在净烟气循环比例为60%、40%、20%的条件下形成的飞灰汞吸附量分别是非烟气循环条件下的3.0、2.3和1.6倍.②烟气循环引起燃烧气体氛围中ρ（SO₂）与ρ（NO）的变化会影响飞灰的物化特性及其汞吸附性能.随燃烧氛围中ρ（SO₂）的提高,飞灰汞吸附量先增后减.烟气循环比例为40%且燃烧气体氛围中ρ（NO）为803 mg/m3条件下,ρ（SO₂）为2 857 mg/m3时褐煤与烟煤燃烧形成的飞灰汞吸附量较高（分别为0.45和0.75 μg/g）,分别较ρ（SO₂）为1 428和4 286 mg/m3时提高了25%~300%和53%~78%.随燃烧氛围中ρ（NO）的提高,飞灰汞吸附量呈逐渐增加趋势.烟气循环比例为40%且燃烧气体氛围中ρ（SO₂）为2 857 mg/m3条件下,ρ（NO）为1 205 mg/m3时褐煤和烟煤燃烧形成的飞灰汞吸附量较高,分别较ρ（NO）为803和402 mg/m3时提高了1.2~3.6和1.1~1.6倍.③飞灰中UBC（未燃尽碳）、CaO、MgO及Fe₂O₃可促进飞灰对汞的吸附.与褐煤飞灰相比,烟煤飞灰表现出更优的汞吸附性能,与UBC、CaO、MgO及Fe₂O₃在飞灰中的含量存在一定的正相关性.研究显示,烟气循环方式下飞灰汞吸附特性发生明显变化,煤质的合理选择、烟气循环比例、循环气体成分及浓度参数的优化控制可显著改善燃煤锅炉烟气中汞的排放控制效果.      

Interaction mechanisms of organic contaminants with burned straw ash charcoal

Black carbons(e.g.,charcoal) have a great impact on the transport of organic contaminants in soil and water because of its strong affnity and ubiquity in the environment.To further elucidate their interaction mechanism,sorption of polar(p-nitrotoluene,m-dinitrobenzene and nitrobenzene) and nonpolar(naphthalene) aromatic contaminants to burned straw ash charcoal under different de-ashed treatments were investigated.The sorption isotherms fitted well with Freundlich equation,and the Freundlich N values were all around 0.31-0.38,being independent of the sorbate properties and sorbent types.After sequential removal of ashes by acid treatments(HCl and HCl-HF) ,both adsorption and partition were enhanced due to the enrichment of charcoal component.The separated contribution of adsorption and partition to total sorption were quantified.The effective carbon content in ash charcoal functioned as adsorption sites,partition phases,and hybrid regions with adsorption and partition were conceptualized and calculated.The hybrid regions increased obviously after de-ashed treatment.The linear relationships of Freundlich N values with the charring-temperature of charcoal or biochar(the charred byproduct in biomass pyrolysis) were observed based on the current study and the cited publications which included 15 different temperatures(100-850°C) ,10 kinds of precursors of charcoal/biochar,and 10 organic sorbates.     

Effects of Acidification and its Mitigation with Lime and Wood Ash on Forest Soil Processes: A Review

Anthropogenic acid deposition causes forest soil acidification and perturbation of the soil forming processes. The impact of soil acidification on tree growth is discussed in view of the role of mycorrhizal fungi in weathering and nutrient uptake. A review has been carried out of experiments involving treatments of forest soil by lime and wood ash, where soil properties and soil solution composition have been investigated. Results from these experiments in Europe and North America are summarized. In general, the content of C in the mor layer decreased as a result of treatment due to higher microbial activity and soil respiration as well as increased leakage of DOC. In addition, the content of N in the mor layer, in general, decreased after treatment and there are occasional peaks of high NO₃concentrations in soil solution. In nearly all reviewed investigations the pH of the deep mineral soil solution decreased and Al, SO₄and NO₃concentrations increased after treatment. These effects are probably due to the high ionic strength and increased microbial activity as a consequence of the treatments. In the soil, pH, CEC and base saturation increased in the upper horizons, but decreases in the upper mineral soil are also reported. In general, there was no increase in tree growth as a result of these treatments. The positive effects of the treatments on soil processes and tree growth are therefore questionable. In view of these conclusions, an investigation was carried out on the soil and soil solution chemistry and the role of mycorrhizal fungi in a spruce stand treated with two doses of lime and another treated with lime/ash in southern Sweden. The results of this investigation is reported in this volume.     

餐厨垃圾的黑水虻处理中含钙矿物及微生物对油脂转化效率的影响

黑水虻处理是近年来发展起来的一种餐厨垃圾的有效资源化方法,但由于黑水虻的生理特性,油脂类物质经常不能被彻底降解和去除,残渣仍有酸败气味,需堆肥化二次处理.为了提高油脂类成分的降解效率,提升黑水虻富集油脂的资源化能力,本研究拟以含钙矿物和微生物为主要辅助手段,通过向餐厨垃圾中添加湿重比例为0~10%的CaCO₃、0~10%的Ca(OH)₂、5%CaCO₃和菌液的混合物及6种不同菌液,研究含钙矿物和微生物对于油脂减量化和虫油转化效率的影响.结果发现,向餐厨垃圾中添加含钙矿物,能够显著调节和缓冲黑水虻处理过程中的环境pH值,但对增加油脂的去除效率和黑水虻油脂的转化能力没有显著作用.而且添加7%~10% 的CaCO₃对于餐厨垃圾的减量化率和黑水虻的虫产率有负作用,添加5%~10%的Ca(OH)₂会导致显著的幼虫死亡率.同时添加CaCO₃和菌液对于油脂的去除不利.仅添加微生物菌液是提高垃圾油脂减量化率和黑水虻油脂富集率的最有效方法.枯草芽孢杆菌NJZ菌株、地衣芽孢杆菌NY菌株、植物乳酸杆菌RS72菌株和粪肠球菌L102菌株,是提高黑水虻油脂转化效率的有效菌株.添加微生物后,黑水虻的虫油产率由对照组的10.4%提升至12.8%~14.4%,虫油富集率由对照组的93.9%提升至116%~130%.虫油富集率超过100%,说明餐厨垃圾中碳水化合物、蛋白质等非油脂成分的一部分转化为黑水虻的体脂,而微生物的辅助降解可能是强化这一过程的主要因素.但即使在接种微生物以后,虫沙中仍然有29%~44%的油脂在处理结束时剩余,说明餐厨垃圾中的油脂较难被彻底降解和利用.未来研究中,可以继续筛选高效降解油脂的微生物,与黑水虻共同处理餐厨垃圾,实现油脂成分的资源化全利用.     

Effects of metal cations on sorption-desorption of p-nitrophenol onto wheat ash

The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however, this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash.     

固化飞灰形状及填埋方式对重金属浸出的影响

为探究成型形状和填埋方式对生活垃圾焚烧飞灰固化体中重金属浸出的影响,设置固化体尺寸分别为10×10×10cm、10×10×2.5cm、DN=3cm（球）,同时设置码放、散乱堆放2种填埋方式进行动态浸出试验.结果表明,在固化体开裂前,球状与长方体、整齐码放与散乱堆放的浸出液pH值存在显著差异;单位质量固化体重金属Pb、Zn、Cr累积浸出量随固液接触面积、堆填散乱度、液固比的增大而增加,固化稳定化飞灰中重金属的浸出符合缩芯模型且主要由扩散过程控制,试验前段Pb、Zn、Cr的2种速率常数与固化体成型比表面积、堆填散乱度、液固比正相关.因此,要减少生活垃圾焚烧厂原灰中重金属的浸出,提高生活垃圾填埋场共处置飞灰固化稳定化产物的安全性,固化体成型时应尽量缩小比表面积同时避免散乱填埋.