碱预处理污泥产酸效果及其生物群落研究

为了提高污泥水解酸化过程中的挥发酸产量,获取污水脱氮除磷所需的内碳源,以深圳市罗芳污水厂的二沉池污泥为研究对象,采用不同的碱量对其进行预处理。通过测定碱预处理污泥水解酸化过程中的挥发酸浓度,并采用聚合酶链式反应-变性梯度凝胶电泳(polymerase chain reaction denature gradient gel electrophoresis,PCR-DGGE)技术对参与碱预处理污泥水解酸化产酸过程的主要微生物种群进行分析,结果表明,当碱投加量为0.20 g NaOH/g VSS时,初始溶出的蛋白浓度为1 780 mg/L;水解酸化15 d时,挥发酸总量达到3 473 mg/L;参与产酸的主要细菌属于Firmicutes、Proteobacteria、Bacteroidetes三个门类。     

Electrogeneration of H(2) for Pd-catalytic hydrodechlorination of 2,4-dichlorophenol in groundwater

A novel electrolytic groundwater remediation process, which used the H₂ continuously generated at cathode to achieve in situ catalytic hydrodechlorination, was developed for the treatment of 2,4-dichlorophenol (2,4-DCP) in groundwater. Catalytic hydrodechlorination using Pd supported on bamboo charcoal and external H₂ showed that 2,4-DCP was completely dechlorinated to phenol within 30 min at pH ? 5.5. In a divided electrolytic system, the catalytic hydrodechlorination of 2,4-DCP in cathodic compartment by H₂ generated at the cathode under 20 and 50 mA reached 100% at 120 and 60 min, respectively. Two column experiments with influent pHs of 5.5 (unconditioned) and 2 were conducted to evaluate the feasibility of this process. The 2,4-DCP removal efficiencies were about 63% and nearly 100% at influent pHs of 5.5 and 2, respectively. Phenol was solely produced by 2,4-DCP hydrodechlorination, and was subsequently degraded at the anode. A low pH could enhance the hydrodechlorination, but was not necessarily required. This study provides the preliminary results of a novel effective electrolytic process for the remediation of groundwater contaminated by chlorinated aromatics.     

Enhanced mercuric chloride adsorption onto sulfur-modified activated carbons derived from waste tires

A number of activated carbons derived from waste tires were further impregnated by gaseous elemental sulfur at temperatures of 400 and 650 degrees C, with a carbon and sulfur mass ratio of 1:3. The capabilities of sulfur diffusing into the micropores of the activated carbons were significantly different between 400 and 650 degrees C, resulting in obvious dissimilarities in the sulfur content of the activated carbons. The sulfur-impregnated activated carbons were examined for the adsorptive capacity of gas-phase mercuric chloride (HgC1) by thermogravimetric analysis (TGA). The analytical precision of TGA was up to 10(-6) g at the inlet HgCl2 concentrations of 100, 300, and 500 microg/m3, for an adsorption time of 3 hr and an adsorption temperature of 150 degrees C, simulating the flue gas emitted from municipal solid waste (MSW) incinerators. Experimental results showed that sulfur modification can slightly reduce the specific surface area of activated carbons. High-surface-area activated carbons after sulfur modification had abundant mesopores and micropores, whereas low-surface-area activated carbons had abundant macropores and mesopores. Sulfur molecules were evenly distributed on the surface of the inner pores after sulfur modification, and the sulfur content of the activated carbons increased from 2-2.5% to 5-11%. After sulfur modification, the adsorptive capacity of HgCl2 for high-surface-area sulfurized activated carbons reached 1.557 mg/g (22 times higher than the virgin activated carbons). The injection of activated carbons was followed by fabric filtration, which is commonly used to remove HgCl2 from MSW incinerators. The residence time of activated carbons collected in the fabric filter is commonly about 1 hr, but the time required to achieve equilibrium is less than 10 min. Consequently, it is worthwhile to compare the adsorption rates of HgCl2 in the time intervals of < 10 and 10-60 min.     

自洁式三级串联的水样在线过滤系统的研制和应用

基于玻璃纤维对小颗粒物的截留和微孔过滤,以及超声波辅助清洗等方法原理,设计和制作了带反冲洗自洁功能的三级串联在线过滤系统,将滤网（初级）、超声波作用下装填有玻璃纤维的过滤器（二级）、微孔滤管（三级）串联,对较高浊度的环境水样进行在线过滤。评估了模拟水样和实际水样中浊度的去除效果,证明该系统对水样中颗粒物有很好的去除并大幅降低水样浊度。在优化的条件下,原始浊度范围在4～100NTU的水样经过滤后,浊度均能降至1NTU以下。以标准方法测定的典型水质指标（活性磷、铵氮、亚硝酸盐氮和硝酸盐氮）的浓度为基准,计算水样经所设计的过滤系统处理后,这4种营养盐的回收率一般在85％-130％之间,说明本系统的使用基本不影响目标物的测定。     

Contamination of organochlorine pesticides in water and sediments from a waterbird-inhabited lake,East Central China

Seventeen organochlorine pesticides (OCPs) were investigated in the water and sediments from a waterbird-inhabited lake (Yangchaihu Lake) to evaluate their current pollution levels and potential risks. The concentrations of total OCPs in water and sediments were 10.12–59.75 ng/l and 4.25–27.35 ng/g dry weight, respectively. Hexachlorocyclohexanes (HCHs) and dichlorodiphenyltrichloroethanes (DDTs) were the most abundant OCPs, while HCB and cyclodiene pesticides were detected with low levels. Levels of ∑OCPs (sum of 17 OCPs) at sites highly influenced by waterbirds were significantly higher than the sites with no significant waterbird populations (one-way ANOVA, P?相似文献   

Characterization of residue from leached cathode ray tube funnel glass: reutilization as white carbon black

Cathode ray tube (CRT) funnel glass remains an urgent environmental problem and is composed mainly of lead oxide and silicon oxide. In this research, the residue could be obtained from 2 h to 500 rpm activated CRT funnel glass after extracting lead via acid leaching under the conditions of HNO₃ concentration 1.0 mol/L, leaching temperature 95 °C and leaching time 1 h. In order to reutilize the residue, its physico-chemical properties were characterized by scanning electron microscopy, Brunauer–Emmett–Teller, thermogravimetric analysis, X-ray diffraction and Fourier transform infrared spectroscopy. The results indicated that the residue was an amorphous superfine powder with approximately 93 wt% silica oxide and specific surface area of more than 170 m²/g. It can be reutilized as white carbon black.     

3种运行模式下CAST工艺脱氮性能

以模拟城市污水为处理对象,采用循环式活性污泥法（CAST）反应器,对3种运行模式（M1：常规模式,M2：缺氧好氧模式、M3：缺氧好氧交替模式）下系统的脱氮性能进行了研究,比较了各模式下CAST反应器的氨氮和总氮的去除效率,并对各模式下典型周期内氮基质浓度变化进行了考察,以确定系统的脱氮模式。结果表明,在氨氮去除不成为限制条件（去除率〉90％）的条件下,3种运行模式下系统总氮的平均去除率分别为67．3％、70．6％和82．4％,以缺氧好氧交替模式下的最高;M1、M2和M3均可实现亚硝酸型硝化,但随着温度的升高,亚硝酸型硝化逐渐消失。静态实验分析表明,3种模式下系统的氨氧化速率大小次序为：vN：M1〉vN：M2〉vN：M3,反硝化速率大小次序为：vDN,M2〉vDN,M3〉vDN,M1。     

水位波动带氮素迁移转化规律

为考察水位波动对非饱和-饱和土层中氮素迁移转化的影响,设计土柱实验装置Ⅰ和Ⅱ分别模拟水位稳定与波动两种情景,测定一个水位波动周期内地下水中NO₃^--N、NO₂^--N和NH₄⁺-N浓度变化情况。结果表明,柱Ⅱ水位第1次下降柱内1^#,2^#,3^#,4^#采样点NO₃^--N浓度均增大,增幅分别为6.5%、14.9%、15.33%和19.8%。水位上升时结果相反,分别降低17.3%、26.15%、50.29%和44.61%。第2次水位下降至初始位置4个采样点NO₃^--N浓度再次增大,幅度分别为7.1%、10.6%、13.89%和7.76%。铵态氮呈相反趋势不同程度的变化。水位波动柱Ⅱ连通水槽内总氮量增加显著高于柱I水槽,即水位波动有利于波动带地下水中氮素垂向迁移,加重波动带以下地下水硝酸盐污染。因此,水位波动对氮素迁移转化的影响不容忽视。     

絮凝#x02014;微波辐射#x02014;Fenton试剂氧化法深度处理焦化废水

用絮凝#x02014;微波辐射#x02014;Fenton试剂氧化法深度处理焦化废水,研究了微波辐射时间、微波功率、FeSO₄加入量、H₂O₂加入量和废水pH对废水处理效果的影响。实验结果表明：在聚合氯化铝加入量为350mg/L、聚丙烯酰胺加入量为12mg/L、废水pH=5、FeSO₄加入量为250mg/L、H₂O₂总加入量为1400mg/L、H₂O₂分3次投加、微波功率为400W、微波辐射时间为60min的条件下,处理后出水的浊度、色度和COD去除率分别为98.59%,97.62%,86.21%。处理后出水澄清透明,COD为50.34mg/L,满足GB50050#x02014;2007《工业循环冷却水处理设计规范》的要求。