野外测量条件对石油污染地下水常规水化学参数的影响

通过原位水质监测仪监测某石油类污染地下水的6项常规水化学指标,研究不同测量方式、不同测量深度对其产生的影响。结果表明:受石油污染的地下水水面以下0.5 m处,原、异位测量的水温、p H值、溶解氧、氧化还原电位、浊度均有不同程度的差异。在对比研究期内,可观测到这种差异最大可达:水温5~6℃,p H值0.2,溶解氧3.0 mg/L,氧化还原电位11 m V,浊度55 NTU。这种地下水环境条件的改变,必然会引起一系列水文地球化学、生物地球化学反应的变化。原位测量水深0.5~4 m范围内,水温随深度增加逐渐增大,最大变幅0.16℃;p H随深度增加变化不大;DO受温度和生化耗氧作用影响,随深度增加而降低;ORP与DO变化趋势大致相同,最大减幅达62 m V;电导率随地下水深度增加其值不变;最大浊度值113 NTU出现在水深4 m处。     

中国地区大气汞的干沉降速度

借助箱模式对汞的干沉降过程进行敏感性分析,并利用区域大气环境模式系统RegAEMS计算中国地区汞干沉降速度的时空分布特征。结果表明,森林下垫面下三类汞（气态零价汞、活性气态汞和颗粒态汞）的干沉降速度较大( 0.13、4.5和0.45 cm·s^-1),水体表面上的相对较小（0.0012,0.5和0.11 cm·s^-1）。敏感性分析发现,三类汞的干沉降速度随着近地层风速增加;降水或者地表湿度降低会导致零价汞和活性气态汞干沉降速度增加;雪盖厚度会减小气态零价汞的干沉降速度而增加活性气态汞的干沉降速度。三类汞的干沉降速度在区域上分布类似,东北以及南部地区最高,华东地区最小。季节变化上,气态零价汞、活性气态汞的干沉降速度在多数下垫面都夏季最大,冬季最小;颗粒态汞季节变化不明显。     

5种卤代乙酰胺类消毒副产物对小鼠淋巴瘤细胞Tk基因致突变性研究

卤代乙酰胺类(HAc Am)消毒副产物(DBPs)是饮用水中新兴含氮类DBPs之一。为探究HAc Ams的致突变性,选择小鼠淋巴瘤细胞作为受试细胞,分别考察了一氯代乙酰胺、二氯代乙酰胺、三氯代乙酰胺、一碘代乙酰胺、二碘代乙酰胺(DIAc Ams)共5种HAc Ams对小鼠淋巴瘤细胞Tk基因突变的影响。结果表明,在0.05~20μmol·L~(-1)暴露浓度下,5种HacAms类DBPs对小鼠淋巴瘤细胞呈现出一定的细胞毒性,随着暴露浓度的升高,细胞毒性增强。暴露4 h后,5种HacAms中只有DIAc-Ams呈现出显著的致突变性(暴露剂量高于5μmol·L~(-1)),且以小集落为主。上述研究结果为研究HacAms对哺乳动物细胞的致突变作用提供了基础数据。     

Deciphering the effect of sodium dodecylbenzene sulfonate on up-flow anaerobic sludge blanket treatment of synthetic sulfate-containing wastewater

• UASB reactor can work efficiently with high COD/SO₄^2- ratios when SDBS exists. • Outcome of the competition between SRB and MPA was affected by SDBS. • Presence of SDBS makes methanogens with H₂/CO₂ as a substrate dominant. • Microbial diversity decreases in the presence of SDBS. In this study, the effects of organic sulfur on anaerobic biological processes were investigated by operating two up-flow anaerobic sludge blanket (UASB) reactors with sodium dodecylbenzene sulfonate (SDBS) as a representative of organic sulfur. The results indicated that the specific methanogenic activity (SMA) and chemical oxygen demand (COD) removal efficiency of R2 (with SDBS added) were higher than those of R1 (without SDBS) when the COD/SO₄²⁻ ratio was above 5.0. However, when the COD/SO₄²⁻ ratio was lower than 5.0, the sulfate reduction efficiency of R2 was higher than that of R1. These results and the observed SDBS transformation efficiency in anaerobic reactors indicate that low concentrations of SDBS accelerate methane production and the continuous accumulation of SDBS does not weaken the reduction of sulfate. Similarly, the calculated electron flux for a COD/SO₄²⁻ ratio of 1.0 indicates that the utilization intensity of electrons by sulfate-reducing bacteria (SRB) in R2 was 36.48% higher than that of SRB in R1 and exceeded that of methane-producing archaea (MPA) under identical working conditions. Moreover, the addition of SDBS in R2 made sulfidogenesis the dominant reaction at low COD/SO₄²⁻, and Methanobacterium and Methanobrevibacter with H₂/CO₂ as the substrate and Desulfomicrobium were the dominant MPA and SRB, respectively. However, methanogenesis was still the dominant reaction in R1, and Methanosaeta with acetic acid as the substrate and Desulfovibrio were the dominant MPA and SRB, respectively.     

G-CNTs/PVDF mixed matrix membranes with improved antifouling properties and filtration performance

A novel nanocomposite OMWCNT-A-GO was synthesized by conjugating OMWCNT and GO. The P-OMWCNT-A-GO membrane was fabricated by non-solvent induced phase inversion. The P-OMWCNT-A-GO exhibits the best water flux, BSA rejection and flux recovery. It should be due to the enhanced membrane pore size, porosity and hydrophilicity. Although carbon nanomaterials have been widely used as effective nanofillers for fabrication of mixed matrix membranes (MMMs) with outstanding performances, the reproducibility of the fabricated MMMs is still hindered by the non-homogenous dispersion of these carbon nanofillers in membrane substrate. Herein, we report an effective way to improve the compatibility of carbon-based nanomaterials with membrane matrixes. By chemically conjugating the oxidized CNTs (o-CNTs) and GO using hexanediamine as cross-linker, a novel carbon nanohybrid material (G-CNTs) was synthesized, which inherited both the advanced properties of multi-walled carbon nanotubes (CNTs) and graphene oxide (GO). The G-CNTs incorporated polyvinylidene fluoride (PVDF) MMMs (G-CNTs/PVDF) were fabricated via a non-solvent induced phase separation (NIPS) method. The filtration and antifouling performances of G-CNTs/PVDF were evaluated using distillate water and a 1 g/L bovine serum albumin (BSA) aqueous solution under 0.10 MPa. Compared to the MMMs prepared with o-CNTs, GO, the physical mixture of o-CNTs and GO and pure PVDF membrane, the G-CNTs/PVDF membrane exhibited the highest water flux up to 220 L/m²/h and a flux recovery ratio as high as 90%, as well as the best BSA rejection rate. The excellent performances should be attributed to the increased membrane pore size, porosity and hydrophilicity of the resulted membrane. The successful synthesis of the novel nanohybrid G-CNTs provides a new type of nanofillers for MMMs fabrication.     

漓江流域岩溶区檵木群落不同恢复阶段物种组成及多样性变化

以空间代替时间的方法选取典型样地,采用常规群落学调查方法对漓江流域岩溶区立地条件基本一致的檵木(Loropetalum chinense)群落不同恢复阶段的植物物种组成及其多样性变化进行研究。结果表明,(1)在所调查的样方中,共记录维管束植物78种,隶属于45科70属。乔木层的建群种檵木随着群落的恢复其重要值有降低的趋势,而在灌木层则相反。檵木群落不同恢复阶段乔木层和灌木层主要优势种为檵木、小巴豆(Croton xiaopadou)、龙须藤(Bauhinia championii)、红背山麻杆(Alchornea trewioides)和紫凌木(Decaspermum esquirolii),草本层主要优势种为狭穗薹草(Carex ischnostachya)、庐山香科科(Teucrium pernyi)和蔓生莠竹(Microstegium fasciculatum)。(2)随着檵木群落的恢复,群落总体、乔木层和灌木层物种丰富度呈现增大的趋势,草本层则相反;Shannon指数和均匀度指数具有一致的变化趋势,乔木层Shannon指数和均匀度指数随檵木群落的恢复呈现增大的趋势,而灌木层、草本层和群落总体则相反。檵木群落不同恢复阶段灌木层Shannon指数均高于乔木层和草本层,而草本层均匀度指数均高于乔木层和灌木层;Simpson指数随檵木群落恢复的变化趋势与Shannon指数和均匀度指数相反。(3)在檵木群落的灌木阶段、乔灌阶段和乔林阶段这3个恢复阶段中,乔灌阶段与乔林阶段之间的乔木层、灌木层、草本层和群落总体的Bray-Curtis指数最大。     

Enhanced electrokinetic remediation of chromium-contaminated soil using approaching anodes

As a new technology used for the cleaning of chromium-contaminated soil, worldwide interest in eletrokinetic (EK) remediation has grown considerably in recent times. However, owing to the fact that chromium exists as both cationic and anionic species in the soil, it is not an efficient method. This paper reports upon a study in which a process using approaching anodes (AAs) was used to enhance the removal efficiency of chromium by eletrokinetics. Two bench-scale experiments to remove chromium from contaminated soil were performed, one using a fixed anode (FA) and the other using AAs. In the AAs experiment, the anode moved toward the cathode by 7 cm every three days. After remediation, soil pH, total chromium, and fractionation of chromium in the soil were determined. The average removal efficiency of total chromium was 11.32% and 18.96% in the FA and AAs experiments, respectively. After remediation, acidic soil conditions throughout the soil were generated through the use of AAs, while 80% of the soil remained neutral or alkalic when using the FA approach. The acidic soil environment and high field intensity in the AAs experiment might have favored chromium desorption, dissolution and dissociation from the soil, plus the mobility of chromium in the soil was also enhanced. The results demonstrate that AAs used in the process of EK remediation can enhance the efficiency of chromium removal from soil.     

Developments in forward osmosis and membrane distillation for desalination of waters

Membrane technology has become a common separation technology over the past decennia. Membranes are used more and more for the production of drinkable water from groundwater, surface water and wastewater. Membranes are now competitive versus conventional techniques. Desalination is predominantly used to eradicate the problem of water scarcity. The sustainability of all desalination processes depends mainly on the reduction of energy costs (production cost) and the increase in water recovery. Forward osmosis and membrane distillation are emerging technologies for sustainable desalination. Here we review membrane processes of forward osmosis and membrane distillation and the advancements in membrane material and modules. We also discuss the capability of membrane distillation in treating highly concentrated aqueous solutions derived from other desalination processes. Furthermore, the advancements in fabrication of high-performance membrane is reviewed and the performance of different membranes and optimization of membrane distillation process are summarized.     

碲化镉量子点(CdTe QDs)对肝细胞的毒性效应及线粒体介导的毒性机制研究

本文探讨了碲化镉量子点(CdTe QDs)对肝细胞的毒性效应及其影响因素,为探索量子点的肝毒性机制提供一定依据。采用人肝癌细胞(Hep G2)和人正常肝细胞(L02)为细胞模型,设置0、25、50和100μmol·L-14个浓度组,采用CCK-8法检测细胞生存率,石墨炉法检测细胞内镉元素含量,采用流式细胞术,装载荧光探针DCFH-DA检测细胞内活性氧水平,采用FITC/PI检测细胞凋亡以及JC-1检测细胞ATP水平。研究结果显示:CdTe QDs诱导2种肝细胞生存率降低,细胞凋亡率升高,细胞对QDs的摄入水平具有时间依赖性,细胞内活性氧水平显著升高,线粒体膜电位降低和ATP含量显著减少,且2种肝细胞比较发现L02细胞损伤程度更为严重。CdTe QDs对2种肝细胞造成损伤,对L02细胞损伤更明显,其原因是L02细胞对CdTe QDs摄取更多,导致进入细胞的QDs引发更为严重的损伤效应。     

硫酸铵细粒子对苯二次有机气溶胶光学特性的影响

苯系物光氧化产生的二次有机气溶胶（SOA）能够散射、吸收大气辐射,扰动区域气候变化.硫酸铵（（NH₄）₂SO₄）是大气中常见的无机细粒子,其大的比表面积可作为半挥发性化合物凝结和反应中心,进而影响SOA的化学组分和光学特性.本文采用烟雾箱研究（NH₄）₂SO₄细粒子对苯SOA在200~600 nm范围内的平均质量吸收系数（mass absorption coefficient,MAC）的影响情况.实验结果表明,低浓度（小于100 μg·m^-3）（NH₄）₂SO₄细粒子仅作为凝结核心,不会影响苯SOA的光学性质.高浓度（大于100 μg·m^-3）（NH₄）₂SO₄细粒子对咪唑类吸光产物的形成有促进作用.苯SOA的MAC值随着（NH₄）₂SO₄细粒子浓度的增加而逐渐增大,却随着细粒子酸度的增大而逐渐减小.水分子的增加会产生更多的NH₄⁺,从而有利于咪唑类化合物的产生,苯SOA的MAC值则随着相对湿度的增加而逐渐增大.而当相对湿度高于70%时,乙二醛水合反应增强,四醇产物脱水、聚合形成的高分子量产物增多,从而导致MAC值减小.这为研究高浓度（NH₄）₂SO₄细粒子背景下,人为源SOA的光学特性提供了实验依据.