碳源及反硝化芽孢杆菌强化低C/N比景观水体的生物脱氮

实验探讨了添加碳源及投加反硝化细菌对低碳氮比景观水体生物脱氮的影响。结果表明,有机碳源及B.subtilis FS05均能显著促进实验水体的生物脱氮作用,实验水体在28℃静置72 h后,乙醇添加组的TN、氨氮、硝酸盐及亚硝酸盐的去除率分别达到了62.7%、67.0%、69.8%和29.4%,而同样条件下,B.subtilis FS05投加组的去除率分别达到了66.9%、73.4%、66.0%和82.2%。从水质变化趋势可以看出,投加B.subtilis FS05能在更短时间内完成生物脱氮过程,其中,硝酸盐和亚硝酸盐去除速率最快,分别仅需要18 h和12 h。     

纯种氨氧化菌短程反硝化特性

以Comamonas aquatica LNL3为研究对象,根据其既能短程硝化又能短程反硝化的特性,采用好氧方式富集和固定化菌种,再以厌氧方式驯化,得到具有高效短程反硝化特性的纯种氨氧化菌。采用扫描电镜对固定化前后的载体进行表征,且用正交试验考察了不同环境因子(温度、pH、碳氮比、溶解氧)对Comamonas aquatica LNL3短程反硝化的影响。结果表明,所用载体与Comamonas aquatica LNL3有良好的亲和性,适于微生物的固定化;环境因子对Comamonas aquatica LNL3短程反硝化影响大小顺序为:温度>pH>DO>C/N;在环境条件改变过程中当温度为35℃,pH=8,C/N=3,DO=2.5 mg/L时,Comamonas aquatica LNL3短程反硝化速率达到最大,为32.63 mg/(L.h);研究结果还表明,Comamonas aquatica LNL3具有好氧反硝化特性,适宜处理低碳氮比废水。     

不同流量分配比对多级A/O工艺去除有机物及脱氮的影响

采用三级A/O工艺分段进水工艺处理低碳源生活污水,考察了进水流量分配比对系统去除有机物、硝化反硝化能力以及去除TN的影响。通过对水质指标沿程监测结果表明,不同流量分配比(4∶3∶3,5∶3∶2,6∶3∶1)对系统去除有机物及硝化效率影响不大,出水COD、氨氮分别均在30 mg/L、1 mg/L以下。但反硝化效果受流量分配比的影响较大,在流量比为5∶3∶2时,有效利用原水中碳源进行反硝化,反硝化效果最好。在流量比为5∶3∶2的情况下,TN出水为5.7 mg/L去除率为82.9%,优于流量分配比为6∶3∶1和4∶3∶3时的脱氮效果。总体而言,分段进水工艺在对碳源的有效利用及能耗节省方面优于单点进水。     

碳源类型及进水量分配对CMICAO工艺脱氮除磷的影响

研究了分别以葡萄糖和乙酸钠为碳源时多点交替进水阶式A2/O(CMICAO)工艺氮磷的去除效果,以及在不同进水C/N比时各进水量分配对脱氮除磷效果的影响.结果表明,在相同的进水COD浓度下,乙酸钠比葡萄糖更适合作为碳源,更能提高脱氮除磷效率.以葡萄糖为碳源时,COD为200 mg/L、C/N比为5、缺氧池与厌氧池进水配比为1∶2时,出水COD、TN、氨氮和TP浓度分别为28.5、10.8、2.1和0.5 mg/L,均达到国家一级A排放标准.若采用葡萄糖作为碳源,投加量以使进水C/N比为5～7.5为宜,外加碳源时缺氧池与厌氧池进水分配比可统一采用1∶1.     

A/O+MBR工艺处理玉米深加工废水的中试研究

实验基于企业污水站的改造工程,研究了MBR对玉米深加工废水的处理效果并对工艺运行参数优化提出建议.结果表明,该工艺对COD的去除率可以达到90％以上,出水稳定在26 mg/L左右;出水NH4-N达到1 mg/L以下;TN去除率达到70％以上,出水TN达到10 mg/L以下,出水完全达到排放标准.通过4种工况的比较,说明在污泥浓度8 g/L左右,曝气池内DO在3 mg/L左右,MBR内DO＞4 mg/L,好氧段停留时间13.5 h,并保证3h以上的缺氧段水力停留段时间的条件下,A/O+ MBR工艺可以有效去除玉米深加工废水中的污染物.     

Global Urban Growth and the Geography of Water Availability,Quality, and Delivery

Globally, urban growth will add 1.5 billion people to cities by 2030, making the difficult task of urban water provisions even more challenging. In this article, we develop a conceptual framework of urban water provision as composed of three axes: water availability, water quality, and water delivery. For each axis, we calculate quantitative proxy measures for all cities with more than 50,000 residents, and then briefly discuss the strategies cities are using in response if they are deficient on one of the axes. We show that 523 million people are in cities where water availability may be an issue, 890 million people are in cities where water quality may be an issue, and 1.3 billion people are in cities where water delivery may be an issue. Tapping into groundwater is a widespread response, regardless of the management challenge, with many cities unsustainably using this resource. The strategies used by cities deficient on the water delivery axis are different than for cities deficient on the water quantity or water quality axis, as lack of financial resources pushes cities toward a different and potentially less effective set of strategies.     

Salting-out phenomenon and 1-octanol/water partition coefficient of metalaxyl pesticide

In this paper, we present the effect of inorganic cations such as Na⁺, K⁺, Ca²⁺, Mg²⁺ on the salting-out phenomenon of metalaxyl from pure water to aqueous salt solutions. Moreover the 1-octanol/water partition coefficient in pure water is presented. To accomplish this, aqueous solubility of metalaxyl was determined in pure water, in different salt solution (NaCl, KCl, CaCl₂ and MgCl₂), and at different concentration level ranging from 0.01 to 1.5 M. The 1-octanol/water partition coefficient was determined using the static shake-flask method. Solubility was determined using dynamic saturation method for pure water in the range of 298.15-325.15 K and at 298.15 K for different salt solutions. The solubility value in pure water for studied interval was found constant (m = 3.118 × 10⁻² mol kg⁻¹).Solubility values were used to calculate the standard molar Gibbs free energy of dissolution (Δ_solG°) and transfer (Δ_trG°) at 298.15 K. The values of Δ_trG° from pure to all studied aqueous salt solutions did not exceed 2 kJ mol⁻¹, the value of Δ_solG° of dissolution is 18.5 ±0.72 kJ mol⁻¹. The 1-octanol/water partition coefficient in pure water log K_o/w is equal to 1.69. The obtained results confirm the classification of the neutral metalaxyl as a slightly hydrophobic molecule.     

Estimation and characterization of PCDD/Fs and dioxin-like PCBs from Chinese iron foundries

The iron foundry industry is considered to be a potential source of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). This study investigated the emission factors and total emission amounts of PCDD/Fs and dioxin-like polychlorinated biphenyls (DL-PCBs) from iron foundries in China. The concentrations and the World Health Organization toxicity equivalents (WHO-TEQs) are presented and the congener profiles are discussed in this paper.In the present work, 26 fly ash samples were collected and tested to quantify the PCDD/Fs and DL-PCBs generated by 14 plants of different scales, and five stack gas samples were collected from two (named as EFG and LFG) of those plants. The emission levels of PCDD/Fs and DL-PCBs indicated that hot-air cupolas had lower emissions than cold-air cupolas. When iron ore lump and sinter were used as raw material, the emission factors were about 250 ng TEQ t⁻¹ of product. However, if the raw material was scrap, the emission factors varied owing to the different contents of organic materials in the raw materials. It was found that the mean WHO-TEQ values of PCDD/Fs and DL-PCBs were 144 and 34.2 pg Nm⁻³ in stack gas and 20.0 and 1.58 pg g⁻¹ in fly ash. In multiple tests, it was estimated that the mean emission factors of PCDD/Fs and DL-PCBs were 365 and 10.9 ng WHO-TEQ t⁻¹ released to residue and 2719 and 555 ng TEQ t⁻¹ released to air. The total emission amounts of PCDD/Fs and DL-PCBs from Chinese iron foundries with cupola furnaces released to residue and air were 16.8 and 146 g WHO-TEQ in 2008, respectively.     

Effect of lipids on sorption/desorption hysteresis in natural organic matter

The chemical composition and physical conformation of natural organic matter (NOM) play a major role in regulating its capacity to retain hydrophobic organic compounds. Naphthalene and phenanthrene were used to study the correlations between sorption/desorption isotherm nonlinearity and compositional data obtained from quantitative ¹³C solid-state DPMAS NMR spectroscopy for soil and peat organic matter with or without lipids. Sorption experiments were conducted using a batch equilibration method. Desorption experiments were carried out immediately following the sorption experiments by three successive decant-refill cycles. Hysteresis was observed in all samples. Nonlinear sorption behavior was increased by removal of lipids from the NOM. The hysteresis index, obtained from the ratio of the Freundlich exponents (N values) for the desorption and sorption isotherms, was lower in the lipid-extracted NOM samples than in the same samples without lipid extraction. The relationship between the extent of hysteresis and the characteristics of the ¹³C DPMAS NMR spectra indicates that altering NOM composition through lipid extraction not only increased the proportion of aromatic-C content, but also increased sorption/desorption hysteresis. Our data also suggest that the hysteresis index is negatively related to aromaticity.     

Air quality assessment by tree bark biomonitoring in urban, industrial and rural environments of the Rhine Valley: PCDD/Fs, PCBs and trace metal evidence

Tree barks were used as biomonitors to evaluate past atmospheric pollution within and around the industrial zones of Strasbourg (France) and Kehl (Germany) in the Rhine Valley. The here estimated residence time for trace metals, PCBs and PCDD/Fs in tree bark is >10 years. Thus, all pollution observed by tree bark biomonitoring can be older than 10 years. The PCB baseline concentration (sum of seven PCB indicators (Σ₇PCB_ind)) determined on tree barks from a remote area in the Vosges mountains is 4 ng g⁻¹ and corresponds to 0.36 × 10⁻³ ng toxic equivalent (TEQ) g⁻¹ for the dioxin-like PCBs (DL-PCBs). The northern Rhine harbor suffered especially from steel plant, waste incinerator and thermal power plant emissions. The polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/Fs) concentrations analyzed in tree barks from this industrial area range between 392 and 1420 ng kg⁻¹ dry-weight (dw) corresponding to 3.9 ng TEQ_PCDD/Fs kg⁻¹ to 17.8 ng TEQ_PCDD/Fs kg⁻¹, respectively. Highest PCDD/F values of 7.2 ng TEQ kg⁻¹ to 17.8 ng TEQ kg⁻¹ have been observed close to and at a distance of <2 km southwest of the chemical waste incinerator. However, very close to this incinerator lowest TEQ dioxin-like PCB (TEQ_DL-PCB) values of 0.006 ng TEQ g⁻¹ have been found. On the other hand close to and southwest and northeast of the steel plant the values are comparatively higher and range between 0.011 ng TEQ g⁻¹ and 0.026 ng TEQ g⁻¹. However, even stronger Σ₇PCB_ind enrichments have been observed at a few places in the city center of Kehl, where ΣDL-PCB values of up to 0.11 ng TEQ g⁻¹ have been detected. These enrichments, however, are the result of ancient pollutions since recent long-term measurements at the same sites indicate that the atmospheric PCB concentrations are close to baseline. Emissions from an old landfill of waste and/or great fires might have been the reasons of these PCB enrichments. Other urban environments of the cities of Kehl and Strasbourg show significantly lower Σ₇PCB_ind concentrations. They suffer especially from road and river traffic and have typically Σ₇PCB_ind concentrations ranging from 11 ng g⁻¹ to 29 ng g⁻¹. The PCB concentration of 29 ng g⁻¹ has been found in tree bark close to the railway station of Strasbourg. Nevertheless, the corresponding TEQ_DL-PCB are low and range between 0.2 × 10⁻³ ng TEQ g⁻¹ and 7 × 10⁻³ ng TEQ g⁻¹. Samples collected near road traffic are enriched in Fe, Sb, Sn and Pb. Cd enrichments were found close to almost all types of industries. Rural environments not far from industrial sites suffered from organic and inorganic pollution. In this case, TEQ_DL-PCB values may reach up to 58 × 10⁻³ ng TEQ g⁻¹ and the corresponding V, Cr, Co, Ni, and Cd concentrations are comparatively high.