A barrier to metal movement: Synchrotron study of iron plaque on roots of wetland plants

正A wetland with attractive plants hosting birds and other wildlife is an esthetically pleasing prospect that is gaining popularity as a way of stabilizing or remediating metalcontaminated soils and sediment(Weber and Gagnon,2014;     

固定化细菌胞壁多糖吸附铜、锌和镍最佳包埋条件的确定

以聚乙烯醇和海藻酸钠为包埋刺,将细菌胞壁多糖进行包埋固定后,以吸附铜、锌和镍的能力为考察指标,从机械强度、传质性和耐酸性等方面综合考虑确定了固定化小球最佳配方。按照此最佳配方进行吸附能力验证实验,结果发现,该固定化小球对铜、锌和镍的吸附量分别达到0．9571mg／g、0．7843mg／g和0．4548mg／g,且机械强度、传质性和耐酸性都较好。     

Air classification of blast furnace dust collected in a fabric filter for recycling to the sinter process

Totally dry cleaning has become a common technology for top gas cleaning in blast furnaces in recent years. A significant advantage of totally dry gas cleaning is that the dust collected is obtained as dry powder, thus simplifying the recycling of the dust in the sinter plant and avoiding aqueous emissions. The concentration of some heavy metals, especially zinc, in the collected dust is usually higher than the maximum tolerable concentration for recycling to the sinter process. Therefore, a process for separation of dust with a low level of contamination from the rest is necessary to make partial recycling possible. This is possible because the limited components are more volatile and accumulate in the finer dust fraction. In wet blast furnace top gas cleaning, hydrocyclones are well established for this separation. For the separation of dry powder from the dry dedusting process air classification can be used. Dust from the top gas of a blast furnace with a fabric filter for dry top gas cleaning was split into several size fractions using a laboratory air classifier. The concentration of Ca, Cd, Cl, Cu, Fe, K, Na, Pb and Zn was analysed for each particle class and the loss on ignition was determined. A strong dependence of the concentration on the particle size was found for the more volatile metals, whereas the Fe and Ca concentration and the loss on ignition were quite evenly distributed. With the calculated recovery–removal-functions the possible recycling rate can be estimated for a given removal rate for the limited components.     

Heavy metal sequential extraction methods--a modification for tropical soils

Sequential extractions of metals can be useful to study metal distributions in various soil fractions. Although several sequential extraction procedures have been suggested in the literature, most were developed for temperate soils and may not be suitable for tropical soils with high contents of Mn and Fe oxides. The objective of this study was to develop a sequential fractionation procedure for Cu and Zn in tropical soils. Extractions were performed on surface (0–20 cm) samples of ten representative soils of Sao Paulo State, Brazil. Chemically reactive Mn forms were satisfactorily assessed by the new modified procedure. Amorphous and crystalline Fe oxides were more selectively extracted in a new two-step extraction. Soil-born Zn and Cu were primarily associated with recalcitrant soil fractions. The proposed procedure provided more detailed information on metal distribution in tropical soils and better characterization of the various components of the soil matrix. The new procedure is expected to be an important tool for predicting the potential effects of environmental changes and land application of metals on the redistribution of chemical forms of metals in tropical soils.     

Recovery of metal values from zinc solder dross

Zinc solder dross containing 14.8% Sn, 16.3% Pb, 0.41% Al and 64.5% Zn was leached with 3% H₂SO₄ at 45°C for 1 h. Zinc and aluminum went into solution, whereas lead and tin remained with the residue. Aluminum was selectively precipitated as calcium aluminum carbonate by treating the sulphate leachate with limestone at pH 4.8. Zinc sulphate solution was either evaporated to obtain zinc sulphate crystals or precipitated as basic zinc carbonate at pH 6.8. The undissolved lead and tin were leached with 5 M hot hydrochloric acid. The major part of lead chloride ( 73%) was separated by cooling the leached products down to room temperature. From the soluble fraction, tin was recovered as hydrated tin oxide by alkylation with caustic soda at pH 2.4, while the remaining lead was separated at pH 8.5 as lead hydroxide. A process flowsheet had been suggested which involved two-stage hydrometallurgical treatment. Parameters affecting the recovery efficiency of the suggested method such as temperature, time, pH and acid: solid stoichiometric ratio were investigated. Results obtained revealed that the optimum leaching conditions were achieved by using 20 ml of 3% H₂SO₄ acid/g dross for 1 h at 45°C. Recovery efficiency of the metal salts was 99.1, 99.4, 99.6 and 99.5% for Zn, Al, Pb and Sn respectively. Recovery efficiency was related to the solubility of the concerned salts under the given experimental conditions.     

原子荧光光谱法同时测定环境水体中痕量锡和锌

采用原子荧光光谱法同时测定环境水样中痕量锡和锌,优化了试验条件。锡在1.00μg/L～10.0μg/L、锌在20.0μg/L～200μg/L范围内线性良好,方法检出限锡为0.13μg/L,锌为1.76μg/L,锡和锌标准溶液测定的相对标准偏差分别为2.9%和4.0%,环境水样加标回收率锡为96.4%～106%,锌为92.0%～111%。     

火焰原子吸收光谱法测定畜禽粪便中铜和锌

采用冻干法-全量酸消解-火焰原子吸收光谱法测定畜禽粪便中铜和锌,优化了试验条件.铜和锌分别在0 mg/L～3.00 mg/L和0 mg/L～1.00 mg/L范围内线性良好,检出限分别为6 mg/kg和2 mg/kg(按取0.5 g试样消解定容至50 mL计算),粪便试样测定的RSD分别为1.3%和3.7%,加标回收率分别为104%和107%.     

Physiological and biochemical characteristic of Miscanthus × giganteus grown in heavy metal – oil sludge co-contaminated soil

The effect of oil sludge and zinc, present in soil both separately and as a mixture on the physiological and biochemical parameters of Miscanthus × giganteus plant was examined in a pot experiment. The opposite effect of pollutants on the accumulation of plant biomass was established: in comparison with uncontaminated control the oil sludge increased, and Zn reduced the root and shoot biomass. Oil sludge had an inhibitory effect on the plant photosynthetic apparatus, which intensified in the presence of Zn. The specific antioxidant response of M. × giganteus to the presence of both pollutants was a marked increase in the activity of superoxide dismutase (mostly owing to oil sludge) and glutathione-S-transferase (mostly owing to zinc) in the shoots. The participation of glutathione-S-transferase in the detoxification of both the organic and the inorganic pollutants was assumed. Zn inhibited the activity of laccase-like oxidase, whereas oil sludge promoted laccase and ascorbate oxidase activities. This finding suggests that these enzymes play a part in the oxidative detoxification of the organic pollutаnt. With both pollutants used jointly, Zn accumulation in the roots increased 6-fold, leading to increase in the efficiency of soil clean-up from the metal. In turn, Zn did not significantly affect the soil clean-up from oil sludge. This study shows for the first time the effect of co-contamination of soil with oil sludge and Zn on the physiological and biochemical characteristics of the bioenergetic plant M. × giganteus. The data obtained are important for understanding the mechanisms of phytoremediation with this plant.     

二溴邻硝基偶氮胂微乳液分光光度法测定水中锌

试验了溴代十六烷基吡啶、正丁醇、正庚烷、水自制微乳溶液体系中，锌与二溴邻硝基偶氮胂的显色反应，建立了分光光度法测定水中锌的方法。在pH值为3.0的乙酸-乙酸钠缓冲溶液中，锌与试剂形成淡红色配合物，其最大吸收峰位于532nm波长处，表观摩尔吸光系数F为1.87×10^5L／（mol·cm）。在显色液中锌的质量浓度在0.003mg／L-0.350mg／L范围内符合比尔定律，检出限为0.001mg／L，水样中锌测定的RSD为1.3％-2.9％，加标回收率为95.7％-102％。     

Coprecipitation mechanisms of Zn by birnessite formation and its mineralogy under neutral pH conditions

Birnessite (δ-Mn(IV)O₂) is a great manganese (Mn) adsorbent for dissolved divalent metals. In this study, we investigated the coprecipitation mechanism of δ-MnO₂ in the presence of Zn(II) and an oxidizing agent (sodium hypochlorite) under two neutral pH values (6.0 and 7.5). The mineralogical characteristics and Zn–Mn mixed products were compared with simple surface complexation by adsorption modeling and structural analysis. Batch coprecipitation experiments at different Zn/Mn molar ratios showed a Langmuir-type isotherm at pH 6.0, which was similar to the result of adsorption experiments at pH 6.0 and 7.5. X-ray diffraction and X-ray absorption fine structure analysis revealed triple-corner-sharing inner-sphere complexation on the vacant sites was the dominant Zn sorption mechanism on δ-MnO₂ under these experimental conditions. A coprecipitation experiment at pH 6.0 produced some hetaerolite (ZnMn(III)₂O₄) and manganite (γ-Mn(III)OOH), but only at low Zn/Mn molar ratios (< 1). These secondary precipitates disappeared because of crystal dissolution at higher Zn/Mn molar ratios because they were thermodynamically unstable. Woodruffite (ZnMn(IV)₃O₇•2H₂O) was produced in the coprecipitation experiment at pH 7.5 with a high Zn/Mn molar ratio of 5. This resulted in a Brunauer–Emmett–Teller (BET)-type sorption isotherm, in which formation was explained by transformation of the crystalline structure of δ-MnO₂ to a tunnel structure. Our experiments demonstrate that abiotic coprecipitation reactions can induce Zn–Mn compound formation on the δ-MnO₂ surface, and that the pH is an important controlling factor for the crystalline structures and thermodynamic stabilities.