“固化赤泥-人工膜”复合防渗材料研究

赤泥本身具有良好的防渗性能,加入石灰作为激发剂,更可提高其防渗性。根据《土工合成材料测试手册》和GB/T 50123—1999《土工试验方法标准》进行渗透试验,结果表明:室内试验在赤泥中加入8%石灰,并夹一层人工防渗膜形成的复合防渗材料,在固化28 d后,其渗透系数可达(7.3～7.4)×10-9 cm/s。在工业试验中,夹入不同厚度和质地的人工防渗膜的石灰(8%)固化赤泥,渗透系数可达到6.32×10-9～1.89×10-7 cm/s。研究成果在中原某铝厂赤泥堆场防渗工程中得到了应用。     

浅海跃层底质对水下声的影响研究

本文针对海底底质对水下噪声传播具有显著影响的现象,选取典型负梯度温度跃层,加载三个典型海底底质,即细砂底质、粉砂底质及黏土-粉砂底质,声波参数为固定值。试验定性分析了浅海海底底质对水下声传播的影响,仿真计算了海底底质对声传播的影响,比较分析了不同底质条件下声波的衰减差异,总结了不同底质对水下声传播影响的特点,并同行参考。     

发酵稻壳对亚铁离子和硫离子的吸附-解吸附特性

为了解发酵稻壳对Fe2+和S2-离子的固定潜力,采用静态批式法研究了发酵稻壳对Fe2+和S2-离子的吸附行为,探讨了反应时间、溶液中Fe2+和S2-浓度、溶液p H、吸附反应环境温度及溶液离子强度对发酵稻壳吸附Fe2+和S2-特性的影响,并进一步通过解吸附试验了解发酵稻壳吸附态Fe2+和S2-的稳定性.结果表明,发酵稻壳吸附Fe2+(r=0.912 1)和S2-(r=0.901 1)的动力学过程均符合Elovich动力学模型,且Fe2+(R2=0.965 1)和S2-(R2=0.936 6)的等温吸附特征可较好地用Freundlich等温吸附模型描述.发酵稻壳对Fe2+和S2-的吸附为非优惠型吸附,其中对Fe2+的吸附为非自发反应,对S2-的吸附为自发反应.发酵稻壳对Fe2+和S2-的吸附过程是一吸热过程,升温有利于吸附作用的进行,发酵稻壳对Fe2+的吸附主要为配位吸附,而对S2-的吸附主要为阴离子交换吸附.一定p H范围内(1.50~11.50)发酵稻壳吸附Fe2+和S2-具有较强的适应性.同时随着离子强度的增加发酵稻壳对Fe2+的吸附量有所增加,而对S2-的吸附量略有减少,进一步证明发酵稻壳对Fe2+的吸附以内层配位为主,对S2-的吸附以外层络合为主.此外,不同p H条件及离子强度下发酵稻壳吸附的Fe2+和S2-解吸率很低,解吸率均小于10.00%.上述结果说明,发酵稻壳对Fe2+和S2-具有较好的吸附能力和环境适应性,吸附态Fe2+和S2-稳定性好,不易再释放.     

嗜盐高效降酚菌株Halomonas sp.H17的筛选及降解苯酚特性

从巴丹吉林沙漠盐湖沉积物中分离获得1株在高盐环境下高效降解苯酚菌H17.分析了H17生理生化特性、16S rDNA基因序列、苯酚降解特性及动力学,结果表明,H17属于盐单胞菌属(Halomonas sp.),能在0～20%的盐度下有效降解苯酚,每升外加适量的碳源(葡萄糖浓度0.8 g)和复合氮源(KNO_3 1 g、NH_4Cl 5 g、酵母提取物0.2 g和胰蛋白胨0.2 g)能够促进H17的生长及降解苯酚能力.在温度为30℃、pH 7～8、盐度5～10%的条件下,H17均能高效降解苯酚,最高降解率可达到88.5%.该菌株降解苯酚动力学符合Halane模型,经拟合其生长参数为μ_(max)=0.31 h~(-1),K_S=191.63 mg·L~(-1),K_i=683.05 mg·L~(-1).研究显示H17具有在高盐环境下降解和耐受苯酚的能力,同时对环境有较强的适应性,体现出其在高盐含酚废水实际处理中具有良好的应用价值.     

FNA对短程硝化污泥菌群结构的影响

在SBR反应器增加游离亚硝酸（FNA）预处理单元,投加浓度为1.2mgHNO₂-N/L的FNA进行缺氧搅拌4.5h,连续处理3d,考察短程硝化污泥中FNA对氨氧化菌（AOB）,丝状菌和微生物菌群结构的影响.研究表明,FNA对AOB有短时抑制作用,并能够抑制优势丝状菌Candidatus_Microthrix（微丝菌属）和Cytophagaceae（噬纤维菌）的增殖,分别由5.1%和1.1%下降到0.78%和几乎不可见.SVI从281mL/g降低到100mL/g左右.NAR能够维持在90%左右,短程硝化不受到破坏.高通量结果显示,FNA处理后微生物菌群结构多样性与丰度出现下降,但Thauera（陶厄氏菌属）和Ottowia出现了增殖,分别增加到5.58%和7.82%,同步硝化反硝化（SND）作用明显,这使得即便只有短程硝化,总氮去除率依然能达到60%以上.     

Development of a model to simulate soil heavy metals lateral migration quantity based on SWAT in Huanjiang watershed, China

Lateral transportation of soil heavy metals in rainfall events could significantly increase the scope of pollution. Therefore, it is necessary to develop a model with high accuracy to simulate the migration quantity of heavy metals. A model for heavy metal migration simulation was developed based on the SWAT(Soil and Water Assessment Tool) model. This model took into consideration the influence of soil p H value, soil particle size, runoff volume, sediment amount,concentration of water-soluble heavy metals dissolved in runoff and insoluble absorbed to the soil particles. This model was reasonable in Huanjiang watershed, Guangxi Zhuang Autonomous Region, south China, covering an area of 273 km~2. The optimal drainage area threshold was determined by analyzing the effects of watershed subdivision on the simulation results to ensure the simulation accuracy. The main conclusions of this paper were:(1) watershed subdivision could affect simulation migration quantity of heavy metals;(2) the quantity of heavy metals transported by sediment accounted for 97%–99% of the total migration quantity in the study watershed. Therefore, sediment played the most important role in heavy metal migration;(3) the optimal drainage area threshold percentage to ensure high simulation accuracy was determined to be 2.01% of the total watershed;(4) with the optimal threshold percentage, this model could simulate the migration quantity of As, Pb and Cd accurately at the total watershed and subwatershed level. The results of this paper were useful for identifying the key regions with heavy metal migration.     

Simultaneous quantification of fifty-one odor-causing compounds in drinking water using gas chromatography-triple quadrupole tandem mass spectrometry

A wide range of compounds with various structural features can cause taste and odor(TO)problems in drinking water. It would be desirable to determine all of these compounds using a simple analytical method. In this paper, a sensitive method combining liquid–liquid extraction(LLE) with gas chromatography-triple quadrupole tandem mass spectrometry(GC–MS/MS)was established to simultaneously analyze 51 odor-causing compounds in drinking water,including organic sulfides, aldehydes, benzenes, phenols, ethers, esters, ketones, nitrogenous heterocyclic compounds, 2-methylisoborneol and geosmin. Three deuterated analogs of target analytes, dimethyl disulfide-d6, benzaldehyde-d6 and o-cresol-3,4,5,6-d4,were used to correct the variations in recovery, and five isotope-labeled internal standards(4-chlorotoluene-d4, 1, 4-dichlorobenzene-d4, naphthalene-d8, acenaphthene-d10, phenanthrene-d10 respectively) were used prior to analysis to correct the variations arising from instrument fluctuations and injection errors. The calibration curves of the target compounds showed good linearity(R2 0.99, level = 7),and method detection limits(MDLs) below 1/10 of the odor threshold concentrations were achieved for most of the odorants(0.10–20.55 ng/L). The average recoveries of most of the analytes in tap water samples were between 70% and 120%, and the method was reproducible(RSD 20%, n = 7). Additionally, concentrations of odor-causing compounds in water samples collected from three drinking water treatment plants(DWTPs) were analyzed by this method.According to the results, dimethyl trisulfide, dimethyl disulfide and indole were considered to be the key odorants responsible for the swampy/septic odor. 2-Methylisoborneol and geosmin were detected as the main odor-causing compounds for musty/earthy odor in DWTP B.     

O池溶解氧水平对石化废水A/O工艺污染物去除效果和污泥微生物群落的影响

以实际石化废水为处理对象,研究溶解氧浓度对A/O反应器生物降解特性的影响.A、B两组反应器平行运行以进行对比,O段的溶解氧浓度分别控制在2~3 mg·L-1和5~6 mg·L-1.反应器稳定运行近半年的结果表明:在HRT为20 h时,A组反应器出水的COD(72.5 mg·L-1±14.8 mg·L-1)略高于B组(68.7 mg·L-1±14.6 mg·L-1),COD平均去除率分别为67.0%和68.8%;出水氨氮的平均浓度和去除率为0.8 mg·L-1和95%左右.出水的BOD5均低于5 mg·L-1.表明A/O反应器对有机物的生物降解比较彻底,溶解氧浓度对其没有显著影响.对O段污泥进行454高通量测序结果表明:变形菌门、浮霉菌门和拟杆菌门细菌所占比例较高,在A、B组反应器中的比例分别为58.7%和59.2%、14.7%和12.7%以及10.8%和12.4%.高溶解氧运行的反应器B具有较高的菌群丰度和多样性,氨氧化菌Nitrosomonas、亚硝酸氧化菌Nitrospira和专性好氧菌如Planctomyces的比例较高.厌氧反硝化菌如Azospira和Acidovora在反应器A中的含量较高.在属的水平,鉴定出的Novosphingobium、Comamonas、Sphingobium和Altererythrobacter属细菌具有降解多环芳烃、氯代硝基苯、农药和石油化合物的功能,有利于石化废水的降解.     

铜、毒死蜱单一与复合暴露对蚯蚓的毒性作用

土壤环境中重金属-农药复合污染已经对土壤生态和人类生存环境构成严重威胁.其中重金属铜和有机磷农药毒死蜱作为土壤环境中两类常见的污染物,其复合污染的环境效应值得关注.本文采用OECD标准滤纸接触法、人工土壤法研究了铜-毒死蜱单一及复合暴露对蚯蚓急性致死作用及回避行为的影响.结果表明,滤纸法和人工土壤法Cu对蚯蚓急性毒性的48h-LC50和14 d-LC50分别为2.23μg·cm-2和496.05 mg·kg-1;而毒死蜱对蚯蚓急性毒性的48 h-LC50和14 d-LC50分别为5.94μg·cm-2和186.07 mg·kg-1.滤纸法和人工土壤法铜、毒死蜱浓度单位配比1∶1时,铜、毒死蜱对蚯蚓急性毒性联合作用类型均近似表现为相加作用,而毒性单位配比1∶1的滤纸法和人工土壤法试验结果分别为协同作用和拮抗作用.回避行为试验结果表明,铜、毒死蜱对蚯蚓回避行为的联合作用类型为拮抗作用.     

微塑料诱导下污泥造粒潜能变化及微生物富集特征

微塑料(MPs)是污水处理厂中普遍检出的新兴污染物之一,目前研究主要集中于传统污水处理系统的污染水平及分布特征,但有关微塑料暴露对污泥颗粒化过程的研究鲜见报道.为探究微塑料对污泥颗粒化的诱导影响,选用环境中广泛检出的聚对苯二甲酸乙二醇酯微塑料(PET-MPs)作为研究对象,通过微塑料暴露试验研究PET-MPs对污泥造粒过程中系统潜能、胞外聚合物(EPS)组成和菌群富集特征的影响.结果表明,PET-MPs暴露显著加快污泥颗粒化进程,同时以蛋白质(PN)为主导的EPS含量上升会增强污泥表面疏水性,造粒速度和EPS分泌量与暴露粒径成正比,微塑料和EPS协同促进颗粒污泥的形成.然而微塑料持续暴露会导致系统除污性能恶化,250μm PET-MPs暴露下亚硝酸盐氮积累的负面影响最严重,浓度高达(5.08±0.24)mg·L^-1.高通量测序结果进一步表明,变形菌门(Proteobacteria)和拟杆菌门(Bacteroidota)是促进颗粒污泥形成的主要优势门;红环菌科(Rhodocyclaceae)、鞘氨醇杆菌科(Sphingomonadaceae)、黄杆菌科(Flavob...