基于流域视角的水环境综合治理规划研究——以江苏省淀山湖为例

以流域为单元进行水资源综合规划和管理是实现水环境改善的重要途径。本文以太湖流域第二大省界湖泊—淀山湖为例,在综合分析流域水环境质量基础上,利用GIS 分析工具划分流域治理片区并制定分区管控策略。根据流域所含骨干河流流向、骨干河流与淀山湖交汇特点、上中下游不同河段及镇域行政边界,将淀山湖流域分为吴淞江流域、千灯浦- 淀山湖流域、昆南湖荡流域、元荡湖荡流域、太浦河流域五大片区138 个子评价单元。通过水环境容量与压力两类空间叠加分析,构建形成污染重点减排区、污染综合治理区、产业绿色化提升区、生态环境保育区等四个类型区域,并提出差异化的产业准入和环境治理措施。本研究不仅为以流域为治理单元的水环境治理规划提供了较为可行的技术体系,而且为太湖流域水环境综合整治思路创新提供了可借鉴的案例。     

煤矿突发事件应急救援的群决策方法

提出了基于直觉模糊集的煤矿突发事件应急救援TOPSIS群决策模型。其中决策者权重采用偏好值与群体平均偏好值的相似度计算,属性指标权重采用直觉模糊熵权法确定。通过直觉模糊加权集成运算将各决策矩阵进行合成得到综合决策矩阵,利用改进后的直觉模糊距离公式计算出全部备选救援方案到正负理想解的距离,根据TOPSIS运算结果可以确定最佳事故救援决策方案。最后通过黑龙江省鸡西某矿的实例分析,验证了该模型的有效性及合理性。     

长江流域春夏旱涝灾害与太平洋海温关联性研究

基于长江流域区域1956-2011年50年气象资料和同期太平洋海温资料,采用Z指数、EOF、REOF、SVD分析等方法,探讨长江流域春季和夏季旱涝特征及其旱涝事件与极端海温异常之间的关联性,得出以下结论。1REOF的Z指数春夏季节旱涝空间分区特征显示,春季前6个模态的累计方差贡献率能够达到61.2%,收敛速度较平缓,夏季前6个模态累积方差贡献率更低,只有52.1%。2前冬太平洋海温的变化与长江流域旱涝的态势呈显著相关关系,春季海温场与长江流域旱涝Z指数场的SVD第一模态显示,长江流域的东北区的旱涝与厄尔尼诺显著相关,当赤道东太平洋海温升高,西太平洋海温降低时,长江流域东北地区偏涝,而长江流域的西部地区偏旱,反之亦然。3夏季海温场与长江流域旱涝Z指数场的SVD第一模态,表明太平洋海温分布主要呈现南北向的分布,当赤道中东太平洋海温偏高,北太平洋海温偏低时,长江流域夏季中部地区偏涝。反之亦然。第二模态,全球海温呈现厄尔尼诺类型的分布,中东太平洋是负相关,而在西太平洋为显著负相关。     

四环素类抗生素和铜复合污染对猪粪厌氧消化的影响

兽用抗生素和矿物元素添加剂可起到预防动物疾病、促进动物生长、提高饲料转化率等作用,因此被广泛应用于畜禽养殖业。本研究以猪粪中温厌氧消化为研究目标,采用全自动甲烷潜势测试系统,考察了一定浓度的四环素(TC:30 mg·kg~(-1)dry weight,DW)、土霉素(OTC:50 mg·kg~(-1)DW)和金霉素(CTC:15 mg·kg~(-1)DW)对厌氧累积产甲烷量和日产甲烷速率的影响。结果表明,TC、OTC和CTC对猪粪中温厌氧消化累积产甲烷量和日产甲烷速率均有促进作用(累积产甲烷总量提高比例分别为7.9%、0.4%和5.4%)。另外,采用超高效液相色谱-四极杆串联质谱对猪粪厌氧消化前后样品中四环素类抗生素及其代谢产物进行了分析。结果表明,液相中的四环素类抗生素在猪粪厌氧消化过程中得到了明显的去除,去除率达到90%~100%;而固相中只有金霉素和差向异构金霉素有明显的去除效果,去除率分别为41.69%和41.58%。采用Tessier连续提取法对猪粪厌氧消化前后样品中5种形态的铜包括可交换态、碳酸盐结合态、铁锰氧化结合态、有机物结合态、残渣态进行了分析,结果表明,猪粪厌氧消化后,可交换态、碳酸盐结合态和铁锰结合态的铜浓度比厌氧消化前分别降低了1%~9%、0.1%~3%、12%~19%,而有机态和残渣态的铜浓度却在厌氧消化后分别增加了15%~35%、1%~2%。厌氧消化后,70%~80%的铜都是以有机铜的形态存在。铜逐渐从不稳定态转化为相对稳定的有机态和残渣态铜,因此,厌氧消化过程使铜从可生物利用态转变为不可生物利用态,趋于稳定化。     

电沉积处理含镉废水的性能研究

电沉积含镉废水考察溶液的不同初始p H、镉的不同初始浓度、电流密度及金属配合物对电沉积效果的影响,利用SEM和XRD对沉积物的表面形貌和物相成分进行分析,研究沉积物金属的存在形式。实验结果表明,p H在1.5~3.5时,溶液中镉的去除效果达到99.3%;一级动力学常数随着初始镉溶液浓度增加而变大;当电流密度为4.46 m A/cm2进行90 min电沉积时反应速率较快且沉积量最大;氨水与镉形成的配合物可以促进电沉积镉的反应速率;对电沉积后的沉积物进行扫描电镜(SEM)和X-射线衍射(XRD)测试。SEM表明,沉积物呈现树枝状的纳米结构。XRD表明,沉积物主要成分为氢氧化镉和镉。     

Enhanced bio-decolorization of 1-amino-4-bromoanthraquinone-2-sulfonic acid by Sphingomonas xenophaga with nutrient amendment

Bacterial decolorization of anthraquinone dye intermediates is a slow process under aerobic conditions. To speed up the process, in the present study, effects of various nutrients on 1-amino-4-bromoanthraquinone-2-sulfonic acid (ABAS) decolorization by Sphingomonas xenophaga QYY were investigated. The results showed that peptone, yeast extract and casamino acid amendments promoted ABAS bio-decolorization. In particular, the addition of peptone and casamino acids could improve the decolorization activity of strain QYY. Further experiments showed that L-proline had a more significant accelerating effect on ABAS decolorization compared with other amino acids. L-Proline not only supported cell growth, but also significantly increased the decolorization activity of strain QYY. Membrane proteins of strain QYY exhibited ABAS decolorization activities in the presence of L-proline or reduced nicotinamide adenine dinucleotide, while this behavior was not observed in the presence of other amino acids. Moreover, the positive correlation between L-proline concentration and the decolorization activity of membrane proteins was observed, indicating that L-proline plays an important role in ABAS decolorization. The above findings provide us not only a novel insight into bacterial ABAS decolorization, but also an L-proline-supplemented bioaugmentation strategy for enhancing ABAS bio-decolorization.     

Controlling cyanobacterial blooms by managing nutrient ratio and limitation in a large hypereutrophic lake: Lake Taihu, China

Excessive nitrogen (N) and phosphorus (P) loading of aquatic ecosystems is a leading cause of eutrophication and harmful algal blooms worldwide, and reducing nutrient levels in water has been a primary management objective. To provide a rational protection strategy and predict future trends of eutrophication in eutrophic lakes, we need to understand the relationships between nutrient ratios and nutrient limitations. We conducted a set of outdoor bioassays at the shore of Lake Taihu. It showed that N only additions induced phytoplankton growth but adding only P did not. Combined N plus P additions promoted higher phytoplankton biomass than N only additions, which suggested that both N and P were deficient for maximum phytoplankton growth in this lake (TN:TP = 18.9). When nutrients are present at less than 7.75-13.95 mg/L TN and 0.41-0.74 mg/L TP, the deficiency of either N or P or both limits the growth of phytoplankton. N limitation then takes place when the TN:TP ratio is less than 21.5-24.7 (TDN:TDP was 34.2-44.3), and P limitation occurs above this. Therefore, according to this ratio, controlling N when N limitation exists and controlling P when P deficiency is present will prevent algal blooms effectively in the short term. But for the long term, a persistent dual nutrient (N and P) management strategy is necessary.     

Acid-assisted hydrothermal synthesis of nanocrystalline TiO2 from titanate nanotubes: Influence of acids on the photodegradation of gaseous toluene

In order to efficiently remove volatile organic compounds (VOCs) from indoor air, onedimensional titanate nanotubes (TiNTs) were hydrothermally treated to prepare TiO₂ nanocrystals with different crystalline phases, shapes and sizes. The influences of various acids such as CH₃COOH, HNO₃, HCl, HF and H₂SO₄ used in the treatment were separately compared to optimize the performance of the TiO₂ nanocrystals. Comparedwith the strong and corrosive inorganic acids, CH₃COOH was not only safer andmore environmentally friendly, but also more efficient in promoting the photocatalytic activity of the obtained TiO₂. Itwasobserved that the anatase TiO₂ synthesized in 15 mol/L CH₃COOH solution exhibited the highest photodegradation rate of gaseous toluene (94%), exceeding that of P25 (44%) by a factor ofmore than two. The improved photocatalytic activity was attributed to the small crystallite size and surface modification by CH₃COOH. The influence of relative humidity (20%-80%) on the performance of TiO₂ nanocrystals was also studied. The anatase TiO₂ synthesized in 15 mol/L CH₃COOH solution was more tolerant tomoisture than the other TiO₂ nanocrystals and P25.     

Insights into metals in individual fine particles from municipal solid waste using synchrotron radiation-based micro-analytical techniques

Excessive inter-contamination with heavy metals hampers the application of biological treatment products derived from mixed or mechanically-sorted municipal solid waste (MSW). In this study, we investigated fine particles of < 2 mm, which are small fractions in MSW but constitute a significant component of the total heavy metal content, using bulk detection techniques. A total of 17 individual fine particles were evaluated using synchrotron radiation-based micro-X-ray fluorescence and micro-X-ray diffraction. We also discussed the association, speciation and source apportionment of heavy metals. Metals were found to exist in a diffuse distribution with heterogeneous intensities and intense hot-spots of < 10 μm within the fine particles. Zn-Cu, Pb-Fe and Fe-Mn-Cr had significant correlations in terms of spatial distribution. The overlapped enrichment, spatial association, and the mineral phases of metals revealed the potential sources of fine particles from size-reduced waste fractions (such as scraps of organic wastes or ceramics) or from the importation of other particles. The diverse sources of heavy metal pollutants within the fine particles suggested that separate collection and treatment of the biodegradable waste fraction (such as food waste) is a preferable means of facilitating the beneficial utilization of the stabilized products.     

Bioreduction of vanadium (V) in groundwater by autohydrogentrophic bacteria: Mechanisms and microorganisms

As one of the transition metals, vanadium (V) (V(V)) in trace amounts represents an essential element for normal cell growth, but becomes toxic when its concentration is above 1 mg/L. V(V) can alter cellular differentiation, gene expression, and other biochemical and metabolic phenomena. A feasible method to detoxify V(V) is to reduce it to V(IV), which precipitates and can be readily removed from the water. The bioreduction of V(V) in a contaminated groundwater was investigated using autohydrogentrophic bacteria and hydrogen gas as the electron donor. Compared with the previous organic donors, H₂ shows the advantages as an ideal electron donor, including nontoxicity and less production of excess biomass. V(V) was 95.5% removed by biochemical reduction when autohydrogentrophic bacteria and hydrogen were both present, and the reduced V(IV) precipitated, leading to total-V removal. Reduction kinetics could be described by a first-order model and were sensitive to pH and temperature, with the optimum ranges of pH 7.5–8.0 and 35–40°C, respectively. Phylogenetic analysis by clone library showed that the dominant species in the experiments with V(V) bioreduction belonged to the β-Proteobacteria. Previously known V(V)-reducing species were absent, suggesting that V(V) reduction was carried out by novel species. Their selective enrichment during V(V) bioreduction suggests that Rhodocyclus, a denitrifying bacterium, and Clostridium, a fermenter known to carry out metal reduction, were responsible for V(V) bioreduction.