三维双阴极-电Fenton法处理腌制酸菜废水的试验研究

采用三维双阴极-电Fenton法处理腌制酸菜废水,通过正交试验考察了酸菜废水中有机物去除的影响因素及其处理效果,并优化了试验条件。试验结果表明:各因素对酸菜废水COD去除率的影响程度大小依次为:pH值电流密度Fe2+用量活性炭用量极板间距电解质Na2SO4用量电解温度;通过对比分析两种电解方式对酸菜废水的处理效果,结果显示三维双阴极-电Fenton法处理酸菜废水时产生的H2O2量、电流效率、溶液中Fe2+浓度以及废水的COD去除率均高于传统单电极-电Fenton法,并分析了反应机理。三维双阴极-电Fenton法用于腌制酸菜废水处理切实可行、效果明显,为实际废水处理提供了参考。     

O3-BAC深度处理工艺中细菌群落时空分布及动态变化规律

为弄清饮用水O₃-BAC深度处理工艺过程中细菌群落的时空分布和动态变化规律,本研究以我国南方某O₃-BAC深度处理工艺水厂为研究对象,采用NovaSeq6000高通量测序技术对夏季和冬季各工艺单元出水及滤砂和活性炭生物膜等细菌群落进行解析.结果表明,出厂水pH、浊度、COD_Mn、菌落总数等指标均满足《生活饮用水卫生标准》（GB5749-2006）的要求.夏季细菌群落多样性明显高于冬季,活性炭生物膜的细菌群落多样性高于滤砂生物膜;混凝沉淀、臭氧化和消毒是影响细菌群落多样性的主要工艺单元.水样和生物膜样品绝对优势菌门均为变形菌门（Proteobacteria）,且主要菌门组成大体相同,但细菌群落门水平相对丰度存在一定的时空差异,属水平上差异则更为明显.此外,检测到的条件致病菌属主要包括芽孢杆菌属（Bacillus）、不动杆菌属（Acinetobacter）、假单胞菌属（Pseudomonas）和分支杆菌属（Mycobacterium）,且其所占核心微生物OTUs数目不受季节性影响.水温和生物可降解溶解性有机碳（BDOC）是显著影响细菌群落分布的主要水质参数.以上研究结果表明,O₃-BAC深度处理工艺过程中细菌群落具有时空变化特性,并可为饮用水微生物安全保障提供支撑.     

微污染饮用水生物过滤影响因素的研究

通过试验探讨了过滤介质、空床接触时间、水温和反冲洗方式对生物过滤去除有机物的影响。试验结果表明 :活性炭、石英砂组成的双层滤料生物滤池对高锰酸盐指数、UV2 5 4的去除效果比无烟煤、石英砂组成的双层滤料滤池和单层石英砂滤料滤池好 ;在一定的范围内 ,随着接触时间或水温的增加 ,各滤柱对高锰酸盐指数的去除率增加 ;加氯水反冲洗方式对生物滤池去除高锰酸盐指数、UV2 5 4的影响比未加氯水反冲洗方式大     

Biodegradation of phthalate esters by two bacteria strains

In this study two aerobic phthalic acid ester (PAE) degrading bacteria strains, DK4 and O18, were isolated from river sediment and petrochemical sludge, respectively. The two strains were found to rapidly degrade PAE with shorter alkyl-chains such diethyl phthalate (DEP), dipropyl phthalate (DPrP), di-n-butyl phthalate (DBP), benzylbutyl phthalate (BBP) and diphenyl phthalate (DPP) are very easily biodegraded, while PAE with longer alkyl-chains such as dicyclohexyl phthalate (DCP) and dihexyl phthalate (DHP) and di-(2-ethylhexyl) phthalate (DEHP) are poorly degraded. The degradation rates of the eight PAEs were higher for strain DK4 than for strain O18. In the simultaneous presence of strains DK4 and O18, the degradation rates of the eight PAEs examined were enhanced. When the eight PAEs were present simultaneously, degradation rates were also enhanced. We also found that PAE degradation was delayed by the addition of nonylphenol or selected polycyclic aromatic hydrocarbons (PAHs) at a concentration of 1 microg/g in the sediment. The bacteria strains isolated, DK4 and O18, were identified as Sphigomonas sp. and Corynebacterium sp., respectively.     

Reactions of compost-derived humic substances with lead, copper, cadmium, and zinc

Thermodynamic stability constants of the formation of complexes from the reactions of humic substances with various metals are usually used as parameters to judge the reactivities of both humic substances and metals. However, in calculating the thermodynamic stability constants, complicated processes for the acquisition of activities of components in reactions are absolutely inevitable. In this study, we investigated the average conditional concentration quotients of the complexes formed from the reaction of metals with humic substances and the relations of these quotients to thermodynamic stability constants. The characterized humic substances including HA (MW>1,000), FA (MW>1,000), and FA (MW<1,000) extracted from a swine compost were prepared to react with Pb, Cu, Cd, and Zn at 25 degrees C and at pH 4.00 and 6.50. Reactions of HA (MW>1,000), FA (MW>1,000), and FA (MW<1,000) with the four metals were carried out at 1:0.1, 1:0.5, 1:1, 1:5, and 1:10 ligand:metal stoichiometry. The concentrations of the free ions of Pb, Cu, Cd, and Zn in the reaction systems of metal-HA suspensions and metal-FA solutions were measured by anodic stripping voltammetry (ASV). The sequence of the average conditional concentration quotients of the formed complexes from the reaction of humic substances with metals was FA(MW<1,000)>FA(MW>1,000)>HA(MW>1,000), showing the relative reactivities of the fractions of swine compost-derived humic substances. The sequence of reacting metals with humic substances was Pb>Cu>Cd>Zn, which is in good agreement with the sequence reported by judging the thermodynamic stability constants. The average conditional concentration quotients of the formed complexes from the reaction of humic substances with metals were thus useful parameters that can be directly related to thermodynamic stability constants and other parameters.     

共存物质对重金属絮凝齐MCC除镉性能的影响

为进一步拓展天然高分子絮凝剂壳聚糖的应用范围,以壳聚糖、L-半胱氨酸为原料,通过酰胺化反应制备一种具有重金属捕集功能的高分子重金属絮凝剂-2-氨基-3-巯基丙酰壳聚糖（MCC）,研究了水体中常见的阴阳离子、有机配位剂及浊度对MCC除镉性能的影响,探讨了絮体形貌与絮体分形维数及絮凝除镉效果间的关系。结果表明,Na＋、Cl-、N03、F-、SO4 2-的存在对MCC除Cd2＋均有促进作用,Ca2＋表现为明显的抑制作用;低浓度的EDTA对除镉有促进作用,随着EDTA浓度的增大,逐渐转为抑制作用;低浓度的腐殖酸对MCC去除Cd2＋有显著的促进作用;在一定范围内,浊度可促进MCC对Cd2＋的去除;絮体间空隙越多,絮体分形维数越小,除镉效果越好。     

化工反应装置危险性分析模式的研究

从近年来化工企业的安全生产事故可以看出,化工生产由于其自身的特点,具有较大的火灾爆炸危险性,因此,正确地对化工企业生产的危险性进行分析,对准确地评价化工企业的安全生产状况非常重要.针对化工企业的安全生产特点,提出了一种针对化工反应装置的危险性分析模式,不仅考虑了生产原料及工艺设备,同时也对工艺过程进行了危险性分析.应用实例表明,该模式对于化工装置的危险性分析具有较强的针对性和可靠性.     

杭州大气颗粒物散射消光特性及霾天气污染特征

2011年7月~2012年6月期间,对大气散射系数、颗粒物浓度及气象因子进行同步观测,以评估颗粒物散射消光对杭州市大气能见度的影响.结果表明,杭州市大气颗粒物散射系数日均值变化范围为108.4~1 098.1 Mm-1,年均值为428.62Mm-1±200.2 Mm-1.散射系数呈明显的季节变化,秋冬高,夏季低.日变化呈典型的双峰型,早峰出现在08:00,晚峰出现在21:00.PM2.5和PM10的散射效率分别为7.6 m2·g-1和4.4 m2·g-1,颗粒物散射消光占总消光比例的90.2%.灰霾和重度灰霾天气下,散射系数分别为684.4 Mm-1±218.1 Mm-1和1 095.4 Mm-1±397.7 Mm-1,达到非霾天气的2.6和4.2倍,表明颗粒物散射消光作用是导致杭州市大气能见度下降和灰霾天气发生的主要因素.     

扬州市不同行政区域空气重金属污染评价

采用活藓监测法,选择广泛分布的小羽藓为材料,对扬州市区、高邮市、仪征市、宝应县4个区域空气中Pb、Zn、Cd、Cr、Ni、Zn、Hg 7种重金属元素污染情况进行监测.利用污染因子分析法、内梅罗综合指数分析法及重金属污染潜在生态风险评价法对不同区域空气重金属危害等级进行评价.结果表明:Zn、Pb、Cd元素主要污染地区为扬州市区,Cu元素主要污染地区为仪征市,Ni、Hg元素主要污染地区为宝应县,Cr元素主要污染地区为高邮市.4个区域空气重金属均处于重度污染水平,存在强生态风险.就整体而言,7种重金属元素中Cd、Zn、Hg为主要污染元素,污染情况最为严重,而Cu、Ni污染程度相对较轻.区域间空气重金属污染特征差别显著,制造业与港口航运发达的南部仪征市、江都区等地比以农业为主的北部宝应县污染重,污染程度由高到低为扬州市区仪征市高邮市宝应县.     

Multi-factors influencing the spatial distribution of polycyclic aromatic hydrocarbons in soils surrounding drinking water protection zone

We selected the Guanting Reservoir in Beijing, China as a case where an industrial area locates on the upwind corner to study the influence of human activities and natural processes on the distribution of polycyclic aromatic hydrocarbons (PAHs) in soils. Soil PAH concentrations in the study area follow a log-normal probability distribution function, suggesting that distribution of PAH in soils was affected by human activities. Distribution of PAHs in soils was significantly affected by the point source that high PAH concentrations were observed in near industrial area with an obvious declining trend from the northwest to the southeast which was the prevailing wind direction in this area. Away from the influence of point source, distribution of PAHs in soils was found to significantly correlate with total organic carbon content, while the influences of agricultural land uses and type of soil texture on the total soil PAHs contents and ring compositions were quite limited. The results can provide some evidences and data on the pollutant accumulation in drink water protection area influenced by natural processes and human activities.