顶流式变径液固流化床的流场分布与分选实验研究

为解决变径水介质分选床中颗粒堆积及细粒级废弃电路板的有效物理分选,在现有的变径水介质分选床下壁面添加了多组顶流管,引入上升水流,加强了壁面堆积物料的松散与分选效果。详细分析了倾斜床体液固两相流的流型变化与特征,并采用ANSYS FLOTRAN CFD软件进行数值模拟,得到了介质流场的压强分布变化规律:流场压强自床体底端至顶端递减,自顶流孔给入的水流可以在床体顶流孔附近形成局部强压区,使分布在床体下壁面的颗粒产生额外的运动加速度。选用≤0.125、0.125~0.250、0.250~0.500mm废弃电路板颗粒进行两因素三水平分选实验,结果表明,采用顶流式变径液固流化床分选系统可实现≤0.500mm废弃电路板中金属成分的有效富集,金属回收率最大达到了93.23%。     

废旧电路板的组成与解离特性研究

废旧印刷电路板是电子废弃物的重要组成部分,含有大量金属、玻璃纤维增强树脂、塑料等有回收利用价值的组分,但处理不当会产生严重污染。在分析中,对细碎到粒度为5mm以下的废旧电路板物料中有价资源的赋存状态和解离特性进行了系统的研究,发现金属与非金属的基本解离粒度为1 2mm,解离度为55. 51%;塑料与其他金属(除铜、铁外)是0. 5mm以上废旧电路板物料中的主要组分,树脂与铜是0 .5mm以下物料中的主要组分;物料中平均金属含量为23. 80%,平均铜含量为5. 78%。     

废印制线路板真空热解渣分选与组成分析的研究

在自行设计制备的真空热解炉中进行了废印制线路板的热解实验,得到固体、液体和气体产物。着重研究了热解固体渣中金属铜和非金属玻璃纤维的物理分选、热解固体渣分析及有氧煅烧对玻璃纤维纯度的影响。结果表明,物理分选效率很高,金属铜的回收率和纯度接近100%;热解固体渣含30.35%的铜、56.21%的玻璃纤维和13.45%的炭黑;有氧煅烧去除炭黑可得到高纯度的玻璃纤维。     

废印刷电路板的静电分选实验研究

金属与非金属材料的分离是回收利用废印刷电路板的关键环节。对废印刷电路板物料的静电分选进行了实验研究。实验以电压、辊筒转速、电晕电极与辊筒之间的距离、静电极位置、电晕电极位置、电晕电极数量等为考察因素,研究各因素对电选效果的影响规律。结果表明,影响金属与非金属材料分离的主要因素是电压、辊筒转速和电晕电极与辊筒之间的距离,对于-0.9 0.45mm的破碎物料,当电压为24kV,辊筒转速为15Hz(54.6r/min),电晕电极与辊筒之间的距离为5.2cm时,得到最大静电分选综合效率67.37%。     

高速粉碎机作用下的电路板真空热解渣破碎特性

首先利用高速粉碎机对大颗粒废弃电路板真空热解渣进行破碎处理,然后采用筛分和颗粒计数法研究破碎产物的破碎规律与解离特性。结果表明,大颗粒废弃电路板真空热解渣在破碎过程中存在着显著的选择性破碎,金属铜主要分布在较粗粒级产物中,玻璃纤维和炭黑则主要分布在较细粒级产物中,并且铜能在较大粒级上实现充分解离;98.64%的铜分布在粒级为0.45~4.0 mm的破碎产物中,而92.05%的玻璃纤维和炭黑分布在粒级为-0.45 mm的破碎产物中;当粒级为-2.0 mm时,铜的解离度达到100%。     

采用Design-Expert软件优化高频气力分选机风量配合设计

采用Design-Expert 7.1.3软件对高频气力分选机的3个风量进行试验方案设计和结果分析.结果表明:在其他操作条件一定的前提下,3个风量对分选效率的影响均为显著;采用Design-Expert 7.1.3软件对3个风量进行正交试验设计,可以有效分析3个风量对高频气力分选机分选效率的影响,并通过试验结果分析建立数学模型,最终得到满足试验要求的风量配合比,最优风量配合比为55∶60∶80.     

上海石洞口第二电厂拟建粉煤灰分选系统的技术可行性研究

上海石洞口第二电厂拟建设粉煤灰分选系统生产国标等级灰,但其粉煤灰的游离氧化钙偏高.研究表明:游离氧化钙在细灰中没有明显富集的趋势,即源灰游离氧化钙含量指标合格,那么分选所产细灰的也合格;供分选用的源灰细度和粒度分布较利于提高分选效率,生产国标Ⅱ级灰的分选产率可达70%左右;建设分选系统在技术上是可行的,且可获得较大的综合效益.     

混凝体系中铝盐水解行为及作用机制的研究与分析

采用Ferron逐时络合比色法对混凝体系中铝盐水解产物分布进行研究发现,铝盐在混凝体系发生水解反应获得的产物中Alb形态含量明显高于纯净水系,并且碱化度越低的铝盐,在适宜pH的混凝体系其水懈产物中Alb形态含量上升越快.而Alc形态含量变化不明显.提出混凝体系中铝盐水解反应的作用机制,指出HCO3-对H+浓度的良好控制是保证铝盐水解反应效率、获取高浓度Alb形态的关键.     

基于NIR混合废塑料识别仪分选效率的模型

通过对近红外光谱(NIRS)识别分选混合废塑料的过程建立数学模型,将经过预处理的废塑料在传送带上的分布分为密集区和稀疏区两大类。以降低分选时间,提高分选效率为研究目的,对影响分选效率的因素进行分析,如分选机所能承受物料密集度上限值θ以及传送带的传输速度V等因素。比较不同θ和V的组合对总分选时间T的影响,通过数值计算并验证,求得最优组合解。研究结果表明:θ的大小影响密集区和稀疏区的面积在总面积中占有量的变化;分选总时间T在θ和V共同变化过程中存在极小值。     

不同形态有机物对自我造粒流化床中颗粒特性的影响

研究了溶解态、胶体态及颗粒态有机物对自我造粒流化床中颗粒特性的影响.研究表明,有机物的形态对颗粒粒径和有效密度有较大影响,即溶解态有机物形成的颗粒粒径最小,胶体态有机物形成的颗粒粒径次之,颗粒态有机物形成的颗粒粒径最大;有效密度规律则相反.此外,颗粒的平均粒径、平均有效密度沿床层高度的变化有不同分布,即自我造粒流化床底部形成的颗粒有效密度最大,但同种原水水质条件下颗粒粒径没有变化规律.     

石膏浆液旋流器的分离性能实验研究

通过理论分析及工程经验对石灰石/石膏法烟气脱硫工艺中石膏浆液脱水系统的旋流器进行优化设计,在与工业实际相近的操作条件下,优选出了一根综合性能较好的旋流器。考察了该旋流器的压力、流量与分离效率之间相互关系,与常规石膏浆液旋流器的分级效率进行了比较,确定了最佳操作条件。结果表明,旋流器的进口流量随着进出口压力差的增大而增大,分离效率随着流量增加先上升后下降。在进口硫石膏颗粒平均粒径为24μm,流量为11.8~14.8 m3/h时,分离效率在85%以上,底流出口10μm、15μm以下的颗粒分别占底流出口颗粒总体积的1%、10%左右,起到了很明显的分级浓缩作用,分离性能也优于常规使用的石膏浆液旋流器。     

粘土矿物材料吸附去除水中痕量邻苯二甲酸酯

研究了天然沸石、2种有机改性沸石及Mg/Al水滑石对水中痕量邻苯二甲酸二甲酯、邻苯二甲酸二(2-乙基己基)酯和邻苯二甲酸二辛酯的等温吸附情况和吸附机理,并与活性炭的吸附性能进行了比较。结果表明,Freundlich和Langmuir吸附等温方程均可以很好地描述天然沸石和Mg/Al水滑石对邻苯二甲酸酯的吸附,2种有机改性沸石对邻苯二甲酸酯的吸附更符合Linear吸附等温方程。与活性炭相比,天然沸石对邻苯二甲酸酯的吸附效果较差;2种有机改性沸石和Mg/Al水滑石对分子尺寸较小的邻苯二甲酸酯物质邻苯二甲酸二甲酯的去除率较低,分别低31.8%、31.4%和19.8%,但对分子较大的邻苯二甲酸酯物质邻苯二甲酸二(2-乙基己基)酯和邻苯二甲酸二辛酯的去除效果相差不大。     

层状氢氧化镁铝对偶氮染料酸性黑10B的脱色性能研究

分别用层状氢氧化镁铝(LDH)和焙烧层状氢氧化镁铝(CLDH)作为吸附剂吸附脱除水溶液中偶氮染料酸性黑10B.考察了脱色时间、pH值、吸附剂的投加量、温度、染料初始浓度和焙烧温度等因素对脱色率的影响.结果表明,LDH及CLDH对酸性黑10B染料具有良好的脱除效果,室温下,10g/L LDH和1g/L的CLDH对浓度为100mg/L的染料的脱色率分别达95.93%和99.97%.pH值是影响吸附能力的关键因素,吸附剂对溶液pH值有一定缓冲作用.LDH及CLDH对酸性黑10B吸附结果符合Langmuir吸附等温式.饱和吸附后的LDH及CLDH用高温热解法再生,吸附性能良好,随再生次数增多,脱色率下降.     

Separation of plastic mixtures using liquid-fluidized bed technology

Separation of heavier-than-water plastic mixtures had been investigated via the fluidization of their packed beds induced by an upward flow of water. The samples examined were resin pellets and crushed plastic products including PVC, PET and PBT. On the onset of a flow, a mixed bed was swelled to the state of fluidization and separated into layers of respective resins depending on their density. The effects of the flow rate, an amount of the samples and their density difference were examined on the separation of resin pellets. Under an appropriate condition, the process was completed within a few minutes, and satisfactory separation was attained when the density difference of the samples exceeded 0.05 g cm-3. By using a column equipped with several sample outlets sorted resins could be recovered with their purity intact by withdrawing each layer successively from above through a suitable outlet. Multi-stage separation was also found to be effective in treating close-density samples. Compared with uniform-sized resin pellets, size distribution of crushed plastic samples deteriorated the separation to some extent.     

Distribution, availability, and sources of trace metals in different particle size fractions of urban soils in Hong Kong: Implications for assessing the risk to human health

The concentration and loading distribution of trace metals (Cu, Zn, Pb, Co, Ni, Cr, and Mn) and major elements (Al, Ca, Fe, and Mg) in different particle size fractions (2000-280, 280-100, 100-50, 50-10, 10-2, and <2 μm) of surface soils from highly urbanized areas in Hong Kong were studied. The enrichment of Pb, Cu, and Zn in the urban soils was strongly influenced by anthropogenic activities, and Pb accumulated in fine particles was mainly derived from past vehicular emissions as shown by Pb isotopic signatures. Trace metals primarily accumulated in clay, fine silt, and very fine sand fractions, and might pose potential health risks via the inhalation of resuspended soil particles in the air (PM₁₀ or PM_2.5), and ingestion of adhered soils through the hand-to-mouth pathway. The mobility, bioavailability, and human bioaccessibility of Pb and Zn in bulk soils correlated significantly with metal concentrations in fine silt and/or very fine sand fractions.     

Attitudes and Responses Towards Air Pollution in Medieval England

ABSTRACT

The concentrations of contaminants in the supply air of mechanically ventilated buildings may be altered by pollutant emissions from and interactions with duct materials. We measured the emission rate of volatile organic compounds (VOCs) and aldehydes from materials typically found in ventilation ducts. The emission rate of VOCs per exposed surface area of materials was found to be low for some duct liners, but high for duct sealing caulk and a neo-prene gasket. For a typical duct, the contribution to VOC concentrations is predicted to be only a few percent of common indoor levels. We exposed selected materials to ~100-ppb ozone and measured VOC emissions. Exposure to ozone increased the emission rates of aldehydes from a duct liner, duct sealing caulk, and neoprene gasket. The emission of aldehydes from these materials could increase indoor air concentrations by amounts that are as much as 20% of odor thresholds. We also measured the rate of ozone uptake on duct liners and galvanized sheet metal to predict how much ozone might be removed by a typical duct in ventilation systems. For exposure to a constant ozone mol fraction of 37 ppb, a lined duct would initially remove ~9% of the ozone, but over a period of 10 days the ozone removal efficiency would diminish to less than 4%. In an unlined duct, in which only galvanized sheet metal is exposed to the air-stream, the removal efficiency would be much lower, ~0.02%. Therefore, ducts in ventilation systems are unlikely to be a major sink for ozone.     

Evaluating the size distribution characteristics and sources of atmospheric trace elements at two mountain sites: comparison of the clean and polluted regions in China

Size-resolved trace metal concentrations at two background sites were assessed during a 1-year observation campaign, with the measurements performed in parallel at two mountain sites, where Mt. Dinghu (DHS) located in the rural region of Pearl River Delta (PRD) and Mt. Gongga (GGS) located in the Tibetan Plateau region. In total, 15 selected trace elements (Mg, Al, K, V, Mn, Fe, Cu, Zn, As, Mo, Ag, Cd, Ba, Tl, and Pb) in aerosol samples were determined using inductively coupled plasma mass spectrometry (ICPMS). The major metals in these two mountain sites were Fe, K, Mg, and Ca with concentrations ranging between 241 and 1452 ng/m³, 428 and 1351 ng/m³, 334 and 875 ng/m³, and 376 and 870 ng/m³, respectively, while the trace metals with the lowest concentrations were Mo, Ag, Cd, and Tl with concentrations lower than 4 ng/m³ in DHS and 2 ng/m³ in GGS. The pronounced seasonal variability in the trace elements was observed in DHS, with lower concentrations in spring and summer and relatively high in winter and autumn, whereas seasonal variance of trace elements is hardly observed in Mt. Gongga. The size distribution pattern of crustal elements of Al, Mg, K, Ba, and Fe was quite similar in DHS and GGS, which were mainly found in coarse particles peaked at 4.7–5.8 μm. In addition, V, Mo, Ag, and Tl were also concentrated in coarse particles, although the high enrichment factor (EF?>?100) of which suggested anthropogenic origin, whereas trace metals of Cd, Mn, Zn, As, Cu, and Pb concentrated in fine mode particles. Specifically, these trace metals peak at approximately 1.5 μm in DHS, while those in GGS peaked at diameter smaller than 0.3 μm, indicating the responsible for long-range transport from the far urban and industrialized areas. Multivariate receptor model combined with the enrichment factor results demonstrated that the trace elemental components at these two background sites were largely contributed from the fossil fuel combustion (55.4% in DHS and 44.0% in GGS) and industrial emissions factors (20.1% vs. 26.5%), which are associated with long distance transport from the coastal area of Southeast China and the Northwestern India, respectively, as suggested by the backward air mass trajectory analysis. Local sources from soil dust contributed a minor variance for trace elements in DHS (9.7%) and GGS (13.8%), respectively.

     

Contamination status and potential release of trace metals in a mangrove forest sediment in Ho Chi Minh City,Vietnam

Can Gio district is located in the coastal area of Ho Chi Minh City, southern Vietnam. Discharge of wastewater from Ho Chi Minh City and neighboring provinces to the rivers of Can Gio has led to concerns about the accumulation of trace metals (As, Cu, Cr, Ni, Pb, and Zn) in the coastal sediments. The main objective of this study was to assess the distribution of As, Cu, Cr, Ni, Pb, and Zn in surface and core sediments and to evaluate the contamination status in relation to local background values, as well as the potential release of these selected trace metals from sediments to the water environment. Sediment characteristization, including determination of fine fraction, pH, organic matter, and major elements (Al, Fe, Ca, K, Mg, and S), was carried out to investigate which parameters affect the trace metal enrichment. Fine fraction and Al contents were found to be the controlling proxies affecting the distribution of trace metals while other sediment characteristics did not show any clear influence on trace metals’ distribution. Although As concentrations in the sediments were much higher compared to its reference value in other areas, the enrichment factor based on local background values suggests minor contamination of this element as well as for Cr, Cu, and Pb. Risk assessment suggested a medium to very high risk of Mn, Zn, and Ni under acidification. Of importance is also that trace metals in sediments were not easily mobilized by organic complexation based on their low extractabilities by ammonium-EDTA extraction.

     

Accumulation of Al, Mn, Fe, Cu, Zn, Cd and Pb by the bryophyte Scapania undulata in three upland waters of different pH.

Measurements were made of the contents of Al, Mn, Fe, Cu, Zn, Cd and Pb in Scapania undulata in three streams (D2, D5, D11) in the English Lake District. The stream waters had average pH values of 5.35 (D2), 5.81 (D5) and 7.26 (D11), the main differences in other major chemical components being in Mg, Al, Ca and alkalinity. There was generally more metal accumulation in the older parts of the plants, but this was not significant in all cases. Extents of accumulation varied with stream pH and dissolved metal concentration. For Al, accumulation was greatest in streams D2 and D5. Mn accumulated most in D5 and Fe was without preference. Cu, Zn and Cd accumulated mostly in the plants in stream D11 and Pb accumulated more in D5 and D11. In terms of enrichment factors (amount of metal in the plants divided by stream water concentration) the sequence was Zn < Cd < Cu < Mn < Pb < Al < Fe. Laboratory experiments supported the findings of the field data, providing evidence that uptake increases with pH at constant total metal concentration. The results are interpreted qualitatively in terms of the chemical speciation of the metals in the stream water and competition between metal ions and protons at the plant-water interface. It is suggested that Al, Cu, Zn, Cd and Pb behave according to chemical complexation, whereas redox processes and/or colloidal interactions may be significant for Mn and Fe.     

介质阻挡放电对湖泊水华蓝藻的去除

采用介质阻挡放电等离子体技术去除太湖水华蓝藻,考察了放电输出功率、空气流速、添加剂(异丙醇、腐植酸)等对蓝藻去除的影响。结果表明,介质阻挡放电能去除太湖水华蓝藻,放电功率100 W,空气流速1.0 L/min,放电18min,在光照强度2 000 lx和25℃下培养4 d,初始叶绿素a浓度为9.58 mg/L藻液中蓝藻去除率达87.8%。增加放电输出功率和空气流速能提高蓝藻的去除效率;腐植酸促进了介质阻挡放电对蓝藻的去除;而异丙醇添加剂抑制了介质阻挡放电的作用。放电处理后,蓝藻细胞内类胡萝卜素含量、SOD活性、MDA含量发生明显变化,介质阻挡放电破坏了蓝藻细胞内含物。