淮河流域安徽省2007年的暴雨洪水特性分析

为系统研究淮河流域安徽省2007年的暴雨洪水特征,对降雨过程和暴雨频率进行了分析.结果表明,2007年的主要暴雨特性是梅雨时间长,梅雨量淮河以北多、淮河以南少,降雨时间长、强度大、范围广,降雨时空分布不均.通过淮河干支流洪水过程和淮河干流洪水特征值的分析,结果表明,2007年的主要洪水特性是水位高、流量大,高水位持续时间长,干支流洪水并发,洪水组合恶劣.虽然淮河干流经过了大规模的治理,2007年洪水期间沿淮启用了蒙洼等9个行蓄洪区,但淮河中游仍然持续高水位,润河集至汪集段超过历史最高洪水位,表明淮河流域洪水灾害较为严重,需要进一步研究如何科学调度沿淮行蓄洪区、如何协调淮河与洪泽湖之间的关系,以便更好地进行该流域的洪水管理.     

Determination of estrogenic compounds in wastewater using liquid chromatography-tandem mass spectrometry with electrospray and atmospheric pressure photoionization following desalting extraction

Two complementary LC-MS ionization methods, electrospray (ESI) and atmospheric pressure photoionization (APPI), have been optimized to determine three natural estrogenic compounds (estrone, 17beta-estradiol and estriol) and two synthetic estrogenic compounds (17alpha-ethynylestradiol and diethylstilbestrol) in the influent and effluent of wastewater treatment plants (WWTPs). The wastewater samples were first subjected to solid-phase extraction coupled with desalting extraction to remove matrix interference. The analytes were then detected using liquid chromatography-tandem mass spectrometry (LC-MS-MS) with ESI and dopant-assisted (DA) APPI to evaluate the ion suppression effect and to complement the detection and quantification of estrogenic compounds in complex wastewater samples. The average ion suppression factors for the extracts of the WWTP influent analyzed using ESI and APPI were 52+/-5% and 27+/-7%, respectively. The sensitivity and ionization efficiency of the LC-ESI-MS-MS system decreased dramatically when a complex matrix was present in the WWTP influent sample. Estrogenic compounds could be detected in the WWTP influent and effluent samples at concentrations below the parts-per-billion level. The lower detection limits obtained when using ESI and the higher matrix tolerance of the APPI method allowed the complete quantification of estrogenic compounds in very complex samples in a complementary manner.     

Correlations between physicochemical properties of PAHs and their distribution in soil, moss and reindeer dung at Ny-Ålesund of the Arctic

Concentrations of 16 polycyclic aromatic hydrocarbons (PAHs) in soil, moss and reindeer dung collected at Ny-Ålesund of the Arctic were measured to investigate their accumulation trends and distribution in the three compartments. Compared with the other regions, the proportions of 2 + 3 ring PAHs to the total PAHs were higher, whereas the proportions of 5 + 6 ring PAHs were lower in the three compartments at Ny-Ålesund. Significant log/log-linear relationship was observed between the sub-cooled liquid vapor pressure and the soil/moss quotient (Q_SM). The relation was similar to the relationship between the gas/particle partition coefficient (K_P) and of PAHs, implying Q_SM would be a “mirror image” of K_P. Excellent log/log-linear relationships were observed between Q_SM and K_OA as well as between the moss/dung quotient (Q_MD) and K_OW. The results presented here indicate the physicochemical properties are suitable for characterizing the distribution of PAHs in soil, moss and reindeer dung.     

NaCl和KCl对厌氧污泥抑制的动力学研究

在厌氧颗粒污泥和厌氧絮状污泥系统中,进行盐质量浓度(NaCl或KCl质量浓度,下同)对厌氧污泥抑制动力学的研究,得到不同拟合的COD降解动力学方程及参数.实验结果表明:当盐质量浓度为10～30 g/L时,KCl对厌氧污泥的COD比降解速率的抑制程度大于NaCl;当盐质量浓度由0 g/L增至10 g/L时,半速率常数逐渐增加;当盐质量浓度由10 g/L增至30 g/L时,半速率常数逐渐减小;在厌氧污泥系统中,NaCl抑制作用下的盐抑制常数高于KCl,且颗粒污泥的盐抑制常数高于絮状污泥.     

电网发展、清洁电源接入与地区能源效率

鉴于我国已经建成全球规模最大的超高压和特高压电网,彻底弥补了电力跨区配置的电网基础设施短板,并且为清洁电源并入电网和跨区消纳提供了完善的基础设施,不仅克服我国电力负荷中心和能源基地的区域布局不协调,而且有益于缓解日益严峻的能源利用率低下和环境污染问题。本文利用1991—2012年全国29个省市面板数据实证研究了清洁电源并网对地区全要素能源效率的影响。为保证实证结果稳健性分别在线性和非线性实证框架下采用系统广义矩估计(SYS-GMM)和面板平滑转换模型(PSTR)两种方法估计了清洁电源接入高压、超高压和特高压电网的地区全要素能源效率异质性效应。实证结果显示:(1)我国电网基础设施对地区全要素能源效率具有明显的增进效应,特别是超高压电网在促进全要素能源效率提升上表现的最为突出,在特高压骨干网架尚未形成的情况下起到了支柱性作用。(2)高压、超高压、特高压与清洁电源交互项的估计系数始终位于负数区间,反映清洁电源并网的能源效率绩效并不明显,受限于并网规模和机制缺陷,还没有发挥出全要素能源效率提升作用。(3)随着人均GDP的不断提高,各等级电网对地区能源效率的益处越来越明显,并且存在着门槛效应。(4)特高压电网对地区能源效率的积极作用主要表现在东部沿海高收入省份,这些省份作为电力消费负荷中心,大规模接入清洁电源对能源效率改善裨益明显。接下来,需要根据地区的能源禀赋结构选择清洁电源的并网模式,完善的电网基础设施、合理的电源结构还需要配置以高效的清洁电源并网机制才能不断增进地区全要素能源效率。     

Competition for electrons between reductive dechlorination and denitrification

It is common that 2,4,6-trichlorophenol (TCP) coexists with nitrate or nitrite in industrial wastewaters. In this work, simultaneous reductive dechlorination of TCP and denitrification of nitrate or nitrite competed for electron donor, which led to their mutual inhibition. All inhibitions could be relieved to a certain degree by augmenting an organic electron donor, but the impact of the added electron donor was strongest for TCP. For simultaneous reduction of TCP together with nitrate, TCP’s removal rate value increased 75% and 150%, respectively, when added glucose was increased from 0.4 mmol?L^–1 to 0.5 mmol?L^–1 and to 0.76 mmol?L^–1. For comparison, the removal rate for nitrate increased by only 25% and 114% for the same added glucose. The relationship between their initial biodegradation rates versus their initial concentrations could be represented well with the Monod model, which quantified their half-maximum-rate concentration (K _S value), and K _S values for TCP, nitrate, and nitrite were larger with simultaneous reduction than independent reduction. The increases in K _S are further evidence that competition for the electron donor led to mutual inhibition. For bioremediation of wastewater containing TCP and oxidized nitrogen, both reduction reactions should proceed more rapidly if the oxidized nitrogen is nitrite instead of nitrate and if readily biodegradable electron acceptor is augmented.

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Insights into the mercury(II) adsorption and binding mechanism onto several typical soils in China

To better understand the Hg(II) adsorption by some typical soils and explore the insights about the binding between Hg(II) and soils, a batch of adsorption and characteristic experiments was conducted. Results showed that Hg(II) adsorption was well fitted by the Langmuir and Freundlich. The maximum adsorption amount of cinnamon soil (2094.73 mg kg^?1) was nearly tenfold as much as that of saline soil (229.49 mg kg^?1). The specific adsorption of Hg(II) on four soil surface was confirmed by X-ray photoelectron spectroscopy (XPS) owing to the change of elemental bonding energy after adsorption. However, the specific adsorption is mainly derived from some substances in the soil. Fourier transform infrared spectroscopy (FTIR) demonstrated that multiple oxygen-containing functional groups (O–H, C=O, and C–O) were involved in the Hg(II) adsorption, and the content of oxygen functional groups determined the adsorption capacity of the soil. Meanwhile, scanning electron microscopy combined with X-ray energy dispersive spectrometer (SEM–EDS) more intuitive revealed the binding of mercury to organic matter, metal oxides, and clay minerals in the soil and fundamentally confirmed the results of XPS and FTIR to further elucidate adsorptive phenomena. The complexation with oxygen-containing functional groups and the precipitation with minerals were likely the primary mechanisms for Hg(II) adsorption on several typical soils. This study is critical in understanding the transportation of Hg(II) in different soils and discovering potential preventative measures.     

Impacts of hydrologic variations on chemical weathering and solute sources in the Min River basin,Himalayan–Tibetan region

Environmental Science and Pollution Research - Feedback between hydrologic variations and chemical weathering is thought to play a crucial role in modulating global carbon cycling. The mechanisms...     

Role of illumination intensity in microcystin development using Microcystis aeruginosa as the model algae

Environmental Science and Pollution Research - Microcystis aeruginosa (M. aeruginosa) is one of the most common genera of cyanobacteria in algal blooms. In the present work, the impact of the...     

Microbial community composition and electricity generation in cattle manure slurry treatment using microbial fuel cells: effects of inoculum addition

Environmental Science and Pollution Research - Microbial fuel cell (MFC) is a sustainable technology to treat cattle manure slurry (CMS) for converting chemical energy to bioelectricity. In this...