外源磷对消落区土壤性质及磷释放的影响

选取三峡库区消落区万州段的紫色冲积土,对消落区土壤添加磷的变化及磷的释放进行实验室模拟试验.结果表明,当外源磷添加量较小(＜50 mgP·kg-1土干重)时,上覆水中磷浓度表现为持续上升.当外源磷添加量较大(＞50 mgP·kg-1土干重)时,在淹水4周左右达到平衡.随着外源磷添加量的增加,无机磷呈增加趋势;Ca2-P,Fe-P,Ca8-P和Al-P增加程度较大;外源磷添加量较大(＞50 mgP·kg-1土)时,O-P也有上升,Ca10-P变化较小.土壤干样与鲜样中磷的最大吸附量(Qm)在不同添加磷情况下变化不显著,磷吸附指数(PSI)、磷最大缓冲能力(MBC)均有显著的下降.表明土壤添加外源磷后土壤有效磷水平增大,同时土壤对磷的吸持能力降低,添加外源磷将增大土壤磷释放的风险.     

NaCl盐度波动对处于污泥膨胀的耐盐脱氮污泥沉降性能的影响

以处于污泥膨胀的耐盐脱氮污泥为研究对象,分别采用有效容积为2和240 L的SBR装置(编号1#和2#),在进水NH3-N浓度为40~100 mg/L,pH为7.45~8.0,溶解氧为3~5 mg/L,温度为28~30℃的条件下,分别研究不同NaCl盐度(0、10、20和30 g/L)对污泥沉降性的影响。实验结果表明,在NaCl盐度条件下,可以明显改善耐盐脱氮污泥的沉降性。NaCl盐度越高,污泥絮凝体体积减小、丝状菌及原生动物减少趋势越明显,污泥沉降性效果越好。在30 g/L盐度时,1#和2#SBR的SV30分别从95%和80%降至53%和30%,SVI分别从185.5和170.8 mL/g降至127.3和78.4 mL/g。     

NaCl盐度波动对处于污泥膨胀的耐盐脱氮污泥沉降性能的影响

以处于污泥膨胀的耐盐脱氮污泥为研究对象,分别采用有效容积为2和240L的SBR装置（编号1#和2#）,在进水NH3-N浓度为40—100mg／L,pH为7．45～8．0,溶解氧为3～5mg／L,温度为28～30℃的条件下,分别研究不同NaCl盐度（0、10、20和30g／L）对污泥沉降性的影响。实验结果表明,在NaCl盐度条件下,可以明显改善耐盐脱氮污泥的沉降性。NaCl盐度越高,污泥絮凝体体积减小、丝状菌及原生动物减少趋势越明显,污泥沉降性效果越好。在30g／L盐度时,1#和2#SBR的SV30分别从95％和80％降至53％和30％,SVI分别从185．5和170．8mL／g降至127．3和78．4mL／g。     

加压混凝沉淀对蓝藻水处理中消毒副产物的控制

为了降低蓝藻水处理中消毒副产物的产生,采用物理加压法取代传统化学氧化法进行预处理,从而减少新的化学物质的产生,降低消毒副产物风险,实验对比研究了加压混凝沉淀和预氧化混凝沉淀除藻工艺中消毒副产物及其前驱物的浓度。结果表明,经0.7 MPa加压1 min后混凝沉淀处理,藻类去除率达到95.8%,浊度0.58 NTU,均比原水混凝沉淀和预氧化混凝沉淀后效果大幅度提高。蓝藻水加压后三卤甲烷前驱物降低26.2%,卤乙酸前驱物无变化,混凝沉淀处理后前驱物比原水混凝沉淀后略有减少。加压水过滤消毒后消毒副产物与原水处理后持平。而经1~2 mg/L的Na Cl O预氧化水混凝沉淀过滤消毒后,三卤甲烷和卤乙酸浓度分别比原水处理后增加了3~4倍和1.7~2.5倍。加压混凝沉淀工艺处理蓝藻水,比传统预氧化工艺更有效控制了消毒副产物的产生。     

Polybrominated diphenyl ethers in plastic products,indoor dust,sediment and fish from informal e-waste recycling sites in Vietnam: a comprehensive assessment of contamination,accumulation pattern,emissions, and human exposure

Residue concentrations of polybrominated diphenyl ethers (PBDEs) in different kinds of samples including consumer products, indoor dust, sediment and fish collected from two e-waste recycling sites, and some industrial, urban and suburban areas in Vietnam were determined to provide a comprehensive assessment of the contamination levels, accumulation pattern, emission potential and human exposure through dust ingestion and fish consumption. There was a large variation of PBDE levels in plastic parts of obsolete electronic equipment (from 1730 to 97,300 ng/g), which is a common result observed in consumer plastic products reported elsewhere. PBDE levels in indoor dust samples collected from e-waste recycling sites ranged from 250 to 8740 ng/g, which were markedly higher than those in industrial areas and household offices. Emission rate of PBDEs from plastic parts of disposed electronic equipment to dust was estimated to be in a range from 3.4 × 10^?7 to 1.2 × 10^?5 (year^?1) for total PBDEs and from 2.9 × 10^?7 to 7.2 × 10^?6 (year^?1) for BDE-209. Some fish species collected from ponds in e-waste recycling villages contained elevated levels of PBDEs, especially BDE-209, which were markedly higher than those in fish previously reported. Overall, levels and patterns of PBDE accumulation in different kinds of samples suggest significant emission from e-waste sites and that these areas are potential sources of PBDE contamination. Intakes of PBDEs via fish consumption were generally higher than those estimated through dust ingestion. Intake of BDE-99 and BDE-209 through dust ingestion contributes a large proportion due to higher concentrations in dust and fish. Body weight normalized daily intake through dust ingestion estimated for the e-waste recycling sites (0.10–3.46 ng/day/kg body wt.) were in a high range as compared to those reported in other countries. Our results highlight the potential releases of PBDEs from informal recycling activities and the high degree of human exposure and suggest the need for continuous investigations on environmental pollution and toxic impacts of e-waste-related hazardous chemicals.     

杭州西湖湖湾生物硅沉积测定与营养演化的过程

选择杭州西湖3处湖湾——茅家埠、乌龟潭、浴鹄湾作为研究对象,通过3处湖湾多点浅钻的表层沉积物生物硅质量分数测试,通过底泥分析西湖疏浚与水环境治理措施的效果。研究发现：对照西湖沉积速率（4mm／a）,3处湖湾表层沉积物中生物硅质量分数高低依次为茅家埠、乌龟潭与浴鹄湾。近10年来不同湖湾沉积物中生物硅沉积含量相差较大,这一时期正对应着西湖综合环境整治工程。对西湖3个湖湾表层沉积物中生物硅质量分数研究表明：西湖水体中的氮、磷、硅促进了硅藻的生长与硅的消耗,不同湖湾之间生物硅沉积存在着明显差异,这可能与人类活动的影响差异有关。     

于桥水库底泥磷分级及其释放能力

取样测定了于桥水库底泥无机磷各组分含量及其平面和竖向分布,无机磷总量为284～704 mg/kg,平均为485.70mg/kg,其中Ca2-p、Cag-P、Al-P、Fe-P、O-P和Ca10-P所占质量分数平均分别为3.5%、2.9%、0.3%、48.5%、2.9%和41.9%.通过模拟释放实验得出,在pH<8和pH=9.10条件下,由于厌氧使得底泥磷释放的启动溶解氧分别为<1、<2 mg/L.底泥磷在pH=6.50、DO<1 mg/L,pH=9.10、DO>5 mg/L,pH=9.10、DO<1 mg/L的3种条件下的极限释放量为0.24、0.17、0.33 mg/g,分别占底泥无机磷总量的41.7%、29.5%和57.3%(质量分数).释放的磷主要来自Fe-P,但Fe-P也只能部分释放.酸性条件下,有部分Ca2-P、CaB-P、Ca10-P和Al-P释放,对于AI-P,低pH酸溶作用要远大于高pH下OH-置换作用.     

球形填料对复合垂直流土地渗滤系统去污效果的生物强化

通过对复合垂直流渗滤系统中增加球型填料,利用生物强化提高系统对城市生活污水污染物去除能力的研究,优化了复合垂直流渗滤系统.并且通过研究,探索了系统非生物作用与生物作用对氮的降解机制.结果表明,通过生物强化系统生活污水中COD的去除率由原来的74.7%提高到85.3%;对NH3-N的去除率由原来的28.7%提高到52.9%;对TN的去除率从31.0%提高到41.7%;系统对TP的去除率由30.9%提高到49.3%.球形填料通过提高系统的硝化活性,增加对氨氮的降解转化效率,同时生物量的大小,也是影响氨氮的降解转化效率的重要因素.系统对污水中氮的降解是以生物作用为主,氮转化以硝化效果较强,反硝化效果比较弱.     

Ultrasound enhanced activation of peroxydisulfate by activated carbon fiber for decolorization of azo dye

Activated carbon fiber (ACF) has become an emerging activator for peroxydisulfate (PDS) to generate sulfate radical (SO₄^??). However, the relative low activation efficiency and poor contaminant mineralization limited its widespread application. Herein, ultrasound (US) was introduced to the ACF activated PDS system, and the synergistic effect of US and ACF in PDS activation and the enhancement of contaminant mineralization were investigated. The synergistic effect of US and ACF was observed in the PDS activation to decolorize orange G (OG). The decolorization efficiency increased with increasing ACF loading and US power, and PDS/OG ratio from 1 to 40. The activation energy was determined to be 24.065 kJ/mol. The radical-induced decolorization of OG took place on the surface of ACF, and both SO₄^?? and hydroxyl radical (^?OH) contributed to OG decolorization. The azo bond and naphthalene ring on OG were destructed to other aromatic intermediates and finally mineralized to CO₂ and H₂O. The introduction of US in the ACF/PDS system significantly enhanced the mineralization of OG. The combination of US and PDS was highly efficient to activate PDS to decolorize azo dyes. Moreover, the introduction of US remarkably improved the contaminant mineralization.