石墨炉原子吸收法测定水中铅的质量控制指标研究

通过对全国9个省份82家实验室监测数据的分析,研究确定了石墨炉原子吸收法测定水中铅的质量控制指标。建议控制值为：标准样品室内相对标准偏差（RSD）≤5.0%,实际样品相对偏差（RD）≤30.0%,标准样品室间相对标准偏差（RSD’）≤10%,标准样品相对误差（RE）≤±8.0%,加标回收率范围为90%～115%,同时还对方法的重复性和再现性指标进行了验证性研究。     

微波消解-GFAAS法测定土壤中的总铅

研究了微波消解-GFAAS法测定土壤样品中总铅的方法。土壤样品加入HNO3+HF,经微波消解体系消解后,在恒温加热器上赶酸并除硅,石墨炉原子吸收光谱法(GFAAS)测定土壤样品中的总铅。测定数据经过与国标(GB/T 17141-1997)消解方法的比对,以及对不同土壤及土壤标准物质的测试。结果表明,两者无显著性差异,且此法重复性好,试剂用量少,安全易控制,结果可靠。     

废FCC催化剂对水中铅离子的连续吸附及脱附

通过测定吸附等温线，考察了Ｐｂ２＋在废ＦＣＣ（流化催化裂化）催化剂上的吸附性能及规律，结果表明，Ｐｂ２＋在废ＦＣＣ催化剂上的吸附规律可用Ｌａｎｇｍｕｉｒ和Ｆｒｕｎｄｌｉｃｈ模式描述，吸附呈单分子层形式且容易进行。又通过填充床吸附试验，对Ｐｂ２＋的连续吸附及脱附情形作了考察。结果表明，在温度为１５℃、ｐＨ为５．１３、过柱速率为３．０ｍＬ／ｍｉｎ、径高比为２．２５．０条件下，吸附柱具备适宜的生产周期，连续吸附操作可行，柱效率可达７５．９％；在温度为１５℃、采用２ｍｏｌ／Ｌ稀盐酸作脱附剂，过柱速率为５．０ｍＬ／ｍｉｎ的条件下，吸附剂易于脱附再生，脱附效率可达７８．１％     

环境中铅的化学循环

本文论述了环境中铅的背景值、来源、污染、质量标准，化学循环包括沉淀溶解、络合解离和吸附解吸以及环境中铅的烷基化，为铅污染治理提供理论依据．     

Understanding the role of nano-TiO2 on the toxicity of Pb on C. dubia through modeling–Is it additive or synergistic?

• A two-compartment model is able to quantify the effect of nano-TiO₂ on Pb toxicity. • Nano-TiO₂ reduces Pb tolerance level and increased the killing rate for C. dubia. • Thus, nano-TiO₂ synergistically enhances Pb toxicity. • Algae reduce Pb transfer rate to the body tissue and the killing rate. Nano-TiO₂ can remarkably increase lead (Pb) toxicity in aquatic organisms. However, the mechanism of this toxicity, additive or synergistic, is not well understood. To explore this mechanism, we inspected the role of nano-TiO₂ in the toxicity of Pb on Ceriodaphnia dubia (C. dubia), a model water flea species typically used for ecotoxicity studies. The effect of algae, a diet for aquatic organisms, on the effect of this binary mixture was also investigated. A two-compartment toxicokinetic (TK)-toxicodynamic (TD) modeling approach was used to quantify the Pb toxicity under these complex conditions and to develop critical parameters for understanding the mechanism of toxicity. This two-compartment modeling approach adequately described the Pb accumulation in the gut and in the rest of the body tissue under different nano-TiO₂ concentrations, with and without algae, and predicted the toxicity response of C. dubia. It indicated that increasing the nano-TiO₂ concentration reduced the Pb tolerance level and concurrently increased the killing rate constant of C. dubia. Therefore, nano-TiO₂ synergistically enhanced Pb toxicity. Algae remarkably reduced the toxicity of this binary mixture through reducing the Pb transfer rate to the body tissue and the killing rate, although it did not affect the Pb tolerance level. This two-compartment modeling approach is useful in understanding the role of nanoparticles when assessing the overall toxicity of nanoparticles and other toxic elements in the environment.     

Ecotoxicity assessment of slag generated in the process of recycling lead from waste batteries

The aim of this study was to evaluate the possible toxicity of the leachate produced by the residues generated in the process of recycling lead from waste batteries. These residues are slag, which once formed, is characterised by its content in ferrous sulphide, sodium carbonate as well as residual coke from the process. It also contains, as minor components, lead and other heavy metals. The slag was stored and watered periodically over a period of 6 months, its composition changing until finally becoming inert, with no exothermal activity. The slag was leached, and its ecotoxicity was determined by means of the bioluminescence test, along with its content in heavy metals. The results obtained indicate a greater degree of toxicity in the residues with a shorter storage period than the established one, and which were therefore still in the phase of decomposition. However, in the samples taken on completing 6 months of storage, the EC₅₀ value of the leachate was found to be higher than 3000 mg/l. Hence, a storage period under suitable environmental conditions which leads to inactivity of the residue as well as a decrease in its ecotoxicity, is considered absolutely essential. At the same time, a direct relationship was observed between the lead content and the ecotoxicity value.     

Concentrations of cadmium and lead heavy metals in Dardanelles seawater

Cadmium and lead were determined simultaneously in seawater by differential pulse stripping voltammetry (DPSV) preceded by adsoptive collection of complexes with 8-hydroxyquinoline (oxine) on to a hanging mercury drop electrode (HMDE). In preliminary experiments the optimal analytical condition for oxine concentration was found to be 2.10⁻⁵ M, at pH 7.7, the accumulation potential was −1.1 V, and the initial scannig potential was −0.8 V. The peak potentials were found −0.652 V for Cd and −0.463 V for Pb At the 60 s accumalation time. The limit of detection (LOD) and limit of quantitatification (LOQ) were found to be by voltammetry as 0.588 and 1.959 μg l⁻¹ (RSD, 5.50%) for Cd and 0.931 and 3.104 μg l⁻¹ (RSD, 4.10%) for Pb at 60 s stirred accumulation time respectively. In these conditions the most of the seawater samples are amenable for direct voltammetric determination of cadmium and lead using a HMDE. An adsorptive stripping mechanism of the electrode reaction was proposed. For the comparison, seawater samples were also analysed by ICP-atomic emission spectrometry method (ICP-AES). The applied voltammetric technique was validated and good recoveries were obtained.     

Northern Idaho House Dust and Soil Lead Levels Compared to the Bunker Hill Superfund Site

House dust has been identified as a major exposure medium for lead (Pb) in children. High levels of Pb in soil and house dust have been recorded at the Bunker Hill Superfund Site (BHSS) in northern Idaho, an historic mining and smelting district. Soil and dust remediation at the site was required; however, regional background soil and dust Pb levels had not been well characterized. The objective of this survey was to determine background house dust Pb levels and to compare those levels with concentrations, and dust and Pb loading rates measured at the BHSS. Soil and house dust samples were collected in five towns demographically similar to the BHSS but unaffected by the mining industry. The background concentrations and loading rates were significantly lower than those observed at the site. House age was a significant factor affecting background soil and house dust Pb concentrations and loading rates.     

Roadside dusts and soils contamination in Cincinnati,Ohio, USA

Roadside dusts and soils were collected from various nonindustrial districts in Cincinnati, Ohio, USA, and analyzed for lead and copper contents. Results showed that the recent lead phase-down action has reduced the level of lead, but the concentrations of both metals are still higher than the background levels for normal soil. Elevated concentrations of copper in heavily traveled highways were noted, suggesting that much of the copper pollutants is probably of automotive origin. The concentration of lead was found to vary with housing age, and higher levels of contamination in the older neighborhoods were observed. This result is probably ascribable to the accumulation of residues from leaded gasoline and lead-based paint in the past and the use of coal fire for space heating in older houses.     

公路两侧土壤中铅的分布规律研究

我们对干线公路两侧土壤中的分布规律进行了研究，得出了公路两土壤铅的一与离公路国边沿的距离符合高斯衰减分布模型，通过比较在正常速率行驶和台速行驶路段的模型参数，对公路两侧土壤中铅含量的影响因素进行了讨论。