快速法与重铬酸钾回流法测定CODcr的比较

通过回流法测定CODcr分析方法与快速法分别对不同水质类型的水样同时测定分析,找出了两者间存在的一些相关性规律.     

Interaction between cadmium,lead and potassium fertilizer (K<Subscript>2</Subscript>SO<Subscript>4</Subscript>) in a soil-plant system

A pot experiment was conducted to examine the influence of potassium (K) fertilizer (K₂SO₄) application on the phytoavailability and speciation distribution of cadmium (Cd) and lead (Pb) in soil. Spring wheat (Triticum aestivum L.) was selected as the test plant. There were seven treatments including single and combined contamination of Cd and Pb. CdCl₂·2.5 H₂O and Pb(NO₃)₂ were added to the soil at the following dosages: Cd + Pb = 0.00 + 0.00, 5.00 + 0.00, 25.0 + 0.00, 0.00 + 500, 0.00 + 1000, 5.00 + 500 and 25.0 + 1000 mg kg⁻¹, denoted by CK, T1, T2, T3, T4, T5 and T6, respectively. The K fertilizer had five levels: 0.00, 50.0, 100, 200 and 400 mg K₂O kg⁻¹ soil, denoted by K0, K1, K2, K3 and K4, respectively. The results showed that the K fertilizer promoted the dry weight (DW) of wheat in all treatments and alleviated the contamination by Cd and Pb. The application of K₂SO₄ reduced the uptake of Cd in different parts including roots, haulms and grains of wheat; the optimum dosage was the K2 level. K supply resulted in a significant (P < 0.05) decrease in the soluble plus exchangeable (SE) fraction of Cd and there was a negative correlation (not significant, P > 0.05) between the levels of K and the SE fraction of Cd in soil. The application of the K fertilizer could obviously restrain the uptake of Pb by wheat and there were significant (P < 0.05) negative correlations between the concentrations of Pb in grains and the levels of K in soil. K supply resulted in a decrease in the SE fraction of Pb (except the K1 level) from the K0 to K4 levels. At the same time, the application of the K fertilizer induced a significant (P < 0.05) decrease in the weakly specifically adsorbed (WSA) fraction of Pb and a significant (P < 0.05) increase in the bound to Fe–Mn oxides (OX) fraction of Pb. At different K levels, the concentration of Pb in the roots, haulms and grains had a positive correlation with the SE (not significant, P > 0.05) and WSA (significant, P < 0.05) fractions of Pb in the soil. All the K application levels in this experiment reduced the phytoavailability of Cd and Pb. Thus, it is feasible to apply K fertilizer (K₂SO₄) to alleviate contamination by Cd and/or Pb in soil. Moreover, the level of K application should be considered to obtain an optimal effect with the minimum dosage.     

两种方法测定地表水总氮结果的探讨

本文使用碱性过硫酸钾消解紫外分光光度法(HJ636-2012)和流动注射-盐酸萘乙二胺分光光度法(HJ668-2013)2种方法对地表水总氮进行对比分析测试,结果显示:流动注射-盐酸萘乙二胺分光光度法测定结果小于碱性过硫酸钾消解紫外分光光度法的测定值。同时对该结果进行了原因分析,为地表水总氮测定方法的选择具有参考价值。     

The application of potassium ferrate for sewage treatment

The comparative performance of potassium ferrate(VI), ferric sulphate and aluminium sulphate for the removal of turbidity, chemical oxygen demand (COD), colour (as Vis400-abs) and bacteria in sewage treatment was evaluated. For coagulation and disinfection of sewage, potassium ferrate(VI) can remove more organic contaminants, COD and bacteria in comparison with the other two coagulants for the same doses used. Also, potassium ferrate(VI) produces less sludge volume and removes more contaminants, which should make subsequent sludge treatment easier.     

DPD分光光度法测定水中游离余氯的探讨

采用DPD分光光度法测定水中的游离余氯,验证了用高锰酸钾替代氯制剂配制标准溶液的有效性,方法在0 mg/L～0.800 mg/L范围内符合朗伯-比尔定律,检出限为0.01 mg/L。使用次氯酸钠标准体系和高锰酸钾标准体系分别测定废水样品及其加标样,并用硫酸亚铁铵滴定法作比对验证,结果显示3种方法具有可比性。     

Seasonal variation in the atmospheric deposition of inorganic constituents and canopy interactions in a Japanese cedar forest

The seasonal changes in throughfall (TF) and stemflow (SF) chemistry and the canopy interactions of K+ and N compounds were studied in a Japanese cedar forest near the Sea of Japan. The fluxes of most ions, including non-sea-salt SO4(2-), from TF, SF, and rainfall showed distinct seasonal trends, increasing from autumn to winter, owing to the seasonal west wind, while the fluxes of NH4+ and K+ ions from TF+SF might have a large effect of canopy interactions. The contact angle (CA) of water droplets on leaves decreased with leaf aging, suggesting that surface wettability increases with leaf age. The K+ concentration in TF was negatively correlated with the CA of 1-year-old leaves, while the NH4+ concentration was positively correlated with the CA. The net fluxes of NH4+ and NO3(-) from TF were positively correlated with the CA. The increase in wettability may accelerate leaching of K+ or uptake of NH4+.     

Cs uptake by four plant species and Cs-K relations in the soil-plant system as affected by Ca(OH)2 application to an acid soil

Three rates of Ca(OH)₂ were applied to an acid soil and the ¹³⁴Cs uptake by radish, cucumber, soybean and sunflower plants was studied. The ¹³⁴Cs concentration in all plant species was reduced from 1.6-fold in the sunflower seeds to 6-fold in the soybean vegetative parts at the higher Ca(OH)₂ rate. Potassium (K) concentration in plants was also reduced, but less effectively. The significantly decreased ¹³⁴Cs-K soil to plant distribution factors (D.F.) clearly suggest a stronger effect of soil liming on ¹³⁴Cs than on K plant uptake. This observation was discussed in terms of ionic interactions in the soil matrix and within the plants. The results also indicated that the increased Ca²⁺ concentration in the exchange phase and in the soil solution along with the improved root activity, due to the soil liming, enhanced the immobilization of ¹³⁴Cs in the soil matrix and consequently lowered the ¹³⁴Cs availability for plant uptake.     

Farmyards, an overlooked source for highly contaminated runoff

Summer sampling of storm runoff generated from areas of roofs and hardstanding situated on four dairy/beef farms has provided novel information regarding its microbiological and chemical quality. All farm hardstandings generated runoff that was contaminated with respect to those pollutants (faecal coliforms, FC, and faecal streptococci, FS, major nutrients, organic carbon) that are ubiquitously associated with faecal matter and urine. The separate analysis of roof runoff indicated that these can contribute significant concentrations of FS, phosphorus (P) and potentially toxic elements such as zinc (Zn), and suggests a level of 'background' contamination originating from wash-off of bird droppings and in the case of Zn galvanised surfaces. On average hardstanding runoff showed enhanced concentrations of >4 orders of magnitude for FC and 2-3 for major nutrients and carbon relative to roof runoff. Organic forms of nitrogen (N) and P contributed significantly (averaging >40%) to the total dissolved fraction in both roof and hardstanding runoff. Part of the substantial variability in composition of runoff samples could be attributed to differences between farms as well as the timing of sample collection during individual storms. Where situations allowed, a comparison of water upstream and downstream of the farmyard demonstrated they acted as a source of multiple contaminants not only during hydrologically active storm events but also during dry periods. Contamination pathways included a combination of both point (e.g., septic overflows) and non-point (e.g., seepage from livestock housing) sources. Farmyards situated within intensive livestock farming areas such as SW Scotland, would be expected to have significant local and accumulated downstream impacts on the aquatic environment. Localised impacts would be particularly important for headwaters and low order streams.     

An ecotoxicological evaluation of aged bottom ash for use in constructions

Municipal and Industrial Solid Waste Incineration (MISWI) bottom ash is mainly deposited in landfills, but natural resources and energy could be saved if these ash materials would be used in geotechnical constructions. To enable such usage, knowledge is needed on their potential environmental impact. The aim of this study was to evaluate the ecotoxicity of leachates from MISWI bottom ash, aged for five years, in an environmental relevant way using a sequential batch leaching method at the Liquid/Solid-ratio interval 1–3, and to test the leachates in a (sub)chronic ecotoxicity test. Also, the leachates were characterized chemically and with the technique of diffusive gradients in thin films (DGTs). By comparing established ecotoxicity data for each element with chemically analysed and labile concentrations in the leachates, potentially problematic elements were identified by calculating Hazard Quotients (HQ). Overall, our results show that the ecotoxicity was in general low and decreased with increased leaching. A strong correspondence between calculated HQs and observed toxicity over the full L/S range was observed for K. However, K will likely not be problematic from a long-term environmental perspective when using the ash, since it is a naturally occurring essential macro element which is not classified as ecotoxic in the chemical legislation. Although Cu was measured in total concentrations close to where a toxic response is expected, even at L/S 3, the DGT-analysis showed that less than 50% was present in a labile fraction, indicating that Cu is complexed by organic ligands which reduce its bioavailability.     

Study of flotation conditions for cadmium(II) removal from aqueous solutions

Flotation conditions for cadmium(II) removal from aqueous solutions were investigated. Precipitate flotation techniques “of the first kind” (PFFK) and “of the second kind” (PFSK) were tested, using potassium ethyl xanthate (KEtX) as a precipitating agent for cadmium(II). The surfactants sodium dodecyl sulfate (SDS) and hexadecyltrimethylammonium bromide (HDTMA) were used as collectors for PFFK. The effects of KEtX and collector concentrations, induction time, bubbling time, solution pH and some foreign ions on cadmium(II) removal were studied. Under optimum conditions, cadmium(II) could be removed by PFFK by ∼93% and >99% using SDS and HDTMA, respectively. By PFSK, removal of about 64% for cadmium(II) was obtained. The two developed precipitate flotation methods were also tested for simultaneous removal of cadmium(II), nickel(II) and cobalt(II) from distilled water and tap water. The effectiveness of PFFK suggests its employment for metal-polluted wastewaters.