Airborne foliar transfer of particular metals in Lactuca sativa L.: translocation,phytotoxicity, and bioaccessibility

The uptake, translocation, and human bioaccessibility of metals originating from atmospheric fine particulate matters (PM) after foliar exposure is not well understood. Lettuce (Lactuca sativa L.) plants were exposed to micronic PbO, CuO, and CdO particulate matters (PMs) by the foliar pathway and mature plants (6 weeks old) were analyzed in terms of: (1) metal accumulation and localization on plant leaf surface, and metal translocation factor (TF) and global enrichment factor (GEF) in the plants; (2) shoot growth, plant dry weight (DW), net photosynthesis (Pn), stomatal conductance (Gs), and fatty acid ratio; (3) metal bioaccessibility in the plants and soil; and (4) the hazard quotient (HQ) associated with consumption of contaminated plants. Substantial levels of metals were observed in the directly exposed edible leaves and newly formed leaves of lettuce, highlighting both the possible metal transfers throughout the plant and the potential for human exposure after plant ingestion. No significant changes were observed in plant biomass after exposure to PbO, CuO, and CdO-PMs. The Gs and fatty acid ratio were increased in leaves after metal exposure. A dilution effect after foliar uptake was suggested which could alleviate metal phytotoxicity to some degree. However, plant shoot growth and Pn were inhibited when the plants are exposed to PbO, and necrosis enriched with Cd was observed on the leaf surface. Gastric bioaccessibility of plant leaves is ranked: Cd?>?Cu?>?Pb. Our results highlight a serious health risk of PbO, CuO, and CdO-PMs associated with consumption of vegetables exposed to these metals, even in newly formed leaves in the case of PbO and CdO exposure. Finally, the study highlights the fate and toxicity of metal rich-PMs, especially in the highly populated urban areas which are increasingly cultivated to promote local food.

     

涡凹气浮(CAF)/SBR法在高寒地区屠宰废水中的应用

采用涡凹气浮(CAF)和序批式活性污泥(SBR)法处理高寒地区屠宰废水,在冬季室温15℃以上培养的活性污泥完全适应该工艺的要求.经该工艺处理后,出水水质可达到国家《污水综合排放标准》(GB 8978-1996)一级标准,COD、BOD5、SS、氨氮和TN去除率分别达到95.3%、96.7%、87.1%、63.3%和60.9%.     

铁炭微电解预处理电路板废水

采用铁炭微电解法预处理电路板废水.结果表明,在进水pH为2.00、铁炭质量比为4:1、振荡时间为20 min的铁炭微电解静态实验最佳条件下,絮凝出水COD去除率为30%;在进水pH为2.00、铁炭质量比为4:1、水力停留时间为50 min的铁炭微电解柱动态实验最佳条件下,连续曝气.絮凝出水COD为11021 mg/L,COD去除率约为34%,BOD5/COD从0.12上升到0.32,可生化性提高,Cu2+质量浓度从9.11 mg/L下降至0.76 mg/L,降低了废水的生物毒性,为生化处理创造了条件.     

Study on the hydrolysis/precipitation behavior of Keggin Al13 and Al30 polymers in polyaluminum solutions

The hydrolysis/precipitation behaviors of Al³⁺, Al₁₃ and Al₃₀ under conditions typical for flocculation in water treatment were investigated by studying the particulates' size development, charge characteristics, chemical species and speciation transformation of coagulant hydrolysis precipitates. The optimal pH conditions for hydrolysis precipitates formation for AlCl₃, PAC_Al13 and PAC_Al30 were 6.5–7.5, 8.5–9.5, and 7.5–9.5, respectively. The precipitates' formation rate increased with the increase in dosage, and the relative rates were AlCl₃ ? PAC_Al30 > PAC_Al13. The precipitates' size increased when the dosage increased from 50 μM to 200 μM, but it decreased when the dosage increased to 800 μM. The Zeta potential of coagulant hydrolysis precipitates decreased with the increase in pH for the three coagulants. The iso-electric points of the freshly formed precipitates for AlCl₃, PAC_Al13 and PAC_Al30 were 7.3, 9.6 and 9.2, respectively. The Zeta potentials of AlCl₃ hydrolysis precipitates were lower than those of PAC_Al13 and PAC_Al30 when pH > 5.0. The Zeta potential of PAC_Al30 hydrolysis precipitates was higher than that of PAC_Al13 at the acidic side, but lower at the alkaline side. The dosage had no obvious effect on the Zeta potential of hydrolysis precipitates under fixed pH conditions. The increase in Zeta potential with the increase in dosage under uncontrolled pH conditions was due to the pH depression caused by coagulant addition. Al–Ferron research indicated that the hydrolysis precipitates of AlCl₃ were composed of amorphous Al(OH)₃ precipitates, but those of PAC_Al13 and PAC_Al30 were composed of aggregates of Al₁₃ and Al₃₀, respectively. Al³⁺ was the most un-stable species in coagulants, and its hydrolysis was remarkably influenced by solution pH. Al₁₃ and Al₃₀ species were very stable, and solution pH and aging had little effect on the chemical species of their hydrolysis products. The research method involving coagulant hydrolysis precipitates based on Al–Ferron reaction kinetics was studied in detail. The Al species classification based on complex reaction kinetic of hydrolysis precipitates and Ferron reagent was different from that measured in a conventional coagulant assay using the Al–Ferron method. The chemical composition of Al_a, Al_b and Al_c depended on coagulant and solution pH. The Al_b measured in the current case was different from Keggin Al₁₃, and the high Al_b content in the AlCl₃ hydrolysis precipitates could not used as testimony that most of the Al³⁺ was converted to highly charged Al₁₃ species during AlCl₃ coagulation.     

新型TCAS吸附树脂对水中Cd2+的吸附去除研究

通过静态吸附试验,研究一种由超分子受体化合物磺化硫杂杯芳烃（TCAS）与树脂结合的产物——新型TCAS吸附树脂对重金属Cd²⁺的吸附去除性能,并初步探讨了吸附机理。试验研究结果表明,TCAS吸附树脂对Cd²⁺的饱和吸附量为14.45 mg/g。当温度为20℃,0.5 g TCAS吸附树脂对10 mL浓度为5 mg/L的Cd²⁺溶液吸附60 min时, Cd²⁺的去除率可达到99%以上。pH值是影响TCAS吸附树脂吸附效果的重要因素,在pH=5～9时,Cd²⁺的去除率随着pH值的升高而增大。在试验范围内,TCAS吸附树脂对Cd²⁺吸附符合Freundlich方程。吸附在TCAS吸附树脂上的Cd²⁺可洗脱回收,TCAS吸附树脂也可再生利用。 TCAS吸附树脂对重金属Cd²⁺的吸附机理主要归因于TCAS对Cd²⁺的络合作用。     

不同高级氧化法对水中低浓度药物甲硝唑降解过程的比较

采用UV、H₂O₂、UV/H₂O₂、Fenton、UV/Fenton和UV/TiO₂方法,对水中低浓度的药物甲硝唑进行降解。通过HPLC和UV-Vis光谱得到的甲硝唑去除率。详细讨论了Fe²⁺、TiO₂和H₂O₂的初始浓度以及溶液的初始pH值对降解效率的影响。结果表明,UV/Fenton和UV/TiO₂ 2种系统对水中低浓度甲硝唑均有很好的去除效果,但前者的光催化效率更高。在甲硝唑浓度=6 μmol/L,H₂O₂和Fe²⁺的初始浓度分别为0.5 mg/L和2.94 μmol/L,pH=4的条件下,UV/Fenton方法对甲硝唑水溶液光催化的最佳效率为95.8%。     

环糊精聚合物对苯胺的吸附和脱附性能研究

以环氧氯丙烷为交联剂,合成和表征了β-环糊精聚合物(β-CDP),从动力学和热力学角度研究了β-CDP对苯胺的吸附性能。研究结果表明,β-CDP对水溶液中的苯胺具有一定的吸附量。用Langmuir, Freundlich和DubininRadushkevich(D-R)吸附等温式拟合了平衡等温数据,并计算出每个模型的参数。苯胺在β-CDP上的吸附符合D-R方程,吸附过程是热力学自发行为。在乙醇中,β-CDP的脱附能力很强,且可循环使用多次。     

炼化企业大检修作业的环保管理

以克拉玛依石化公司为例,对检修作业前环境危害因素进行了辨识,提出了检修前、检修期间环保管理的措施,从废气、废水、噪声、固废四个方面详细介绍了大检修期间进行污染控制的具体措施,分析了大型炼化企业在停工大检修作业期间存在的环境影响因素,提出了大检修作业期间的环保管理内容及污染控制措施。     

Effective removal of coordinated copper from wastewater using a new dithiocarbamate-type supramolecular heavy metal precipitant

A new dithiocarbamate-type heavy metal precipitant, sodium 1,3,5-hexahydrotriazinedithiocarbamate (HTDC), was prepared and used to remove coordinated copper from wastewater. In the reported dithiocarbamate-type precipitants, HTDC possesses the highest percentage of the effective functional groups. It could effectively precipitate copper to less than 0.5 mg l⁻¹ from both synthetic and actual industrial wastewater containing CuEDTA in the range of pH 3–9. UV–vis spectral investigation and elemental analysis suggested that the precipitate was a kind of coordination supramolecular compound, [Cu₃(HTDC)₂]_n. The toxicity characteristic leaching procedure (TCLP) and semi-dynamic leaching test (SDLT) indicated that the supramolecular precipitate was non-hazardous and stable in weak acid and alkaline conditions. Tests of an anion exchange resin D231 provided a clue to simultaneously remove excess HTDC and residual CuEDTA in practical process of wastewater treatment.     

Biosorption properties of Cd(II), Pb(II), and Cu(II) of extracellular polymeric substances (EPS) extracted from Aspergillus fumigatus and determined by polarographic method

Extracellular polymeric substances (EPS) were extracted from Aspergillus fumigatus using cationic exchange resin technique. The EPS were mainly composed of polysaccharide and low quantities of protein and nucleic acid. Biosorption of Cd(II), Pb(II), and Cu(II) of EPS was investigated as a function of pH using differential pulse polarography and the Ruzic model. Results showed that the EPS biosorption capacity determined using either the direct titration curves i?=?f(C _M) or the method proposed by Ruzic (Analytica Chimica Acta 140:99–113, 1982) were coincident. Cu(II) had the highest affinity with EPS followed by Pb(II) and Cd(II). The total number of binding sites for Cu(II) and Cd(II) increased with pH in the range of 4.0–7.0. Similar trend was observed for Pb(II) at pH?4.0–5.0, while precipitates were observed at pH?6.0 and 7.0. The conditional binding constants of these three metals displayed low levels of fluctuation with pH and ranged from 4.02?±?0.02 to 5.54?±?0.05.