不同碳源在污水处理过程中的变化规律研究

通过对A2/O污水处理工艺长期的分析监测,探明了城市污水处理厂原水中有机物不同生物降解性及碳源赋存形态比例.原水中大部分有机物以颗粒态存在,占进水有机物的61%.原水中快速、慢速、难生物降解有机物比例分别为15.8%、54.2%和30%,快速生物降解有机物主要以溶解态存在,慢速生物降解有机物则主要以颗粒态存在.通过快速、慢速生物降解有机物的沿程监测分析,明确了两种碳源在污水处理过程中的变化规律,厌氧池与缺氧池内均存在微生物水解发酵引起的慢速生物降解有机物的转化作用,其中厌氧反应池的转化效率最高.分析计算了污水处理过程中不同碳源的转化,明确了快慢速有机物在各单元的转化和利用情况,结果指出,2 h内慢速生物降解有机物在厌氧池与好氧池转化率分别为33%和20%.从脂肪酸的种类及含量来说,厌氧池与缺氧池的脂肪酸的种类及含量均高于原水.     

Volatile halogenated organics in swimming pools

This survey undertaken in Greece (Mytilene town) has shown that Volatile halogenated organics (VHO) are present in swimming pool water. Analysis was performed by purge‐and‐trap (PAT) gas chromatographic (GC) technique and samples from two public indoor swimming pools in Mytilene were analyzed for VHO. Water samples were collected every week for a period of three months, and have shown the occurrence of chloroform, dichlorobromomethane, chlorodi‐bromomethane, bromoform (all four are trihalomethanes [THMs]), as a result of the chlorination and the occurrence of tetrachloroethylene and 1,1,1,2‐tetrachloroethane is assigned to their introduction as impurities during the process treatment of water. The levels of concentrations ranged from 4.0 to 26.0 μg/1 for chloroform, from 0.26 to 7.0 μg/1 for dichlorobromomethane, from 0.5 to 3.0 μg/1 for chlorodibromomethane, from 0.07 to 0.9 μg/1 for bromoform, from no detectable levels to 0.07 μg/1 for tetrachloroethylene and from no detectable levels to 0.2 μg/1 for 1,1,1,2‐tetrachloroethane.     

Contamination of Oxygen-Consuming Organics in the Yellow River of China

Contamination of oxygen-consuming organics (OCOs) was one of the most serious problems in the Yellow River of China. This study was conducted to analyze monitoring of the data on OCOs contamination for the river in 1980 and during 1992–1999 as well as examining the effect of suspended solids (SS) on chemical oxygen demand (COD_Mn) and biochemical oxygen demand (BOD₅) of river water. Several significant results have arisen from the study. First, COD_Mn and BOD₅ of the river water showed an increasing trend from the upper to the lower reaches of the mainstream. BOD₅ values of river water in 1992 were significantly higher than those in 1980 and showed an increasing trend during 1992–1999. Second, OCOs in river water of the mainstream was attributed mainly to point sources; the ratio of point to non-point sources of BOD₅ was about 2.81. The load from point sources showed an increasing trend during 1992–1998. In contrast, the load from non-point sources manifested a decreasing trend during this period; this was caused by the decreasing trend of SS content in river water. The total load of BOD₅ from point and non-point sources displayed an increasing trend during 1992–1998. Third, as the humic substances in SS can hardly be biologically oxidized in natural conditions but can be oxidized by chemical oxidants such as potassium permanganate, COD_Mn was not suitable for being regarded as a parameter reflecting the pollution degree of OCOs in river water with a high SS content.     

焦炉烟气中苯可溶物分析方法探讨

根据现有国家标准方法，通过改进实验条件，在保证了实验数据准确度的前提下，在样品量大和时间紧的情况下，可缩短回流时间，提高分析效率，作到保质保量。     

Concurrent Chemical and Histological Analyses: Are They Compatible?

Bivalves are often used as sentinel organisms in monitoring programmes for trace organic contaminants. the animal's physiological state may be important in interpreting trends in contaminant body burden. Simultaneous evaluation of physiological state and organic contaminant concentration in bivalves typically involves removal of a lipid-rich cross-section of the body mass for histopathological and/or gonadal analysis.

In this study, the bias introduced by this technique in the final trace organic concentrations, e.g. of polynuclear aromatic hydrocarbons, chlorinated pesticides and polychlorinated biphenyls, are evaluated on five different size groups of oysters. As a test case, we evaluated the use of this method in the NOAA's Status & Trends Mussel Watch (NS&T) Programme. the average biases introduced by this technique in the final trace organic concentrations in Gulf of Mexico oysters have been increasing since 1986 as a consequence of a continuous decrease in the size of the individuals sampled.     

泥炭预处理吸附垃圾渗滤液中的COD

通过对泥炭改性去除水中COD进行了试验研究。探讨了磷酸、硫酸、盐酸、硝酸和氢氧化钠对COD去除效果的影响和吸附机理。结果表明,在酸、碱改性过程中,用5%的硫酸改性的泥炭去除COD的效果最佳,改性泥炭用量为每10 g/100 mL,吸附时间为60 min,pH为10的试验条件下,COD的去除率为68.5%以上,磷酸较硫酸次之,去除率为55%左右,而盐酸和硝酸较差分别为45%和38%,氢氧化钠为40%左右。并对其吸附机理进行了研究,其吸附等温线符合Freundlich型。通过扫描电镜观察泥炭表面的结构,硫酸改性后的泥炭表面结构比较粗糙,比表面积最大,与实验结果相吻合。用原子吸收法对泥炭处理前后的水样进行比较,表明泥炭对重金属也有很好的去除率。本研究为泥炭利用提供了可借鉴的思路。     

染料探针技术对二级出水中优势污染物的定量检测

分别以刚果红和中性红为染料探针,建立了牛血清蛋白质(BSA)和海藻酸多糖(SA)含量与共振光散射(RLS)发射光谱强度间的线性关系;以甲苯胺蓝为染料探针,建立了腐殖酸(HA)含量与紫外吸光度间的线性关系;优化了3种标准物质的检测浓度范围及溶液p H值条件;考察了染料探针分析方法对标准物的二元和三元混合样品中的回收率.结果表明在适宜的浓度范围内,BSA、HA、SA浓度与染料探针光谱强度间的线性相关系数R0.98,3种标准物在混合样品中的回收率不小于95%,标准误差低于0.11%.以紫外光谱和3D-EEM光谱特征作为城市污水二级出水样品中蛋白质、多糖和腐殖酸的定性依据,确认了4种二级出水样品中的优势污染物.通过染料-探针技术与国标法测得的多糖和蛋白质质量浓度的相对偏差在1.2%~0.04%之间.     

污泥超声破解效应及厌氧消化性能研究

针对超声破解污泥的可行性进行了实验研究,重点考察了超声频率、比能耗、作用时间等因素对破解效应的影响,探讨了破解污泥的厌氧消化性能。结果表明,超声作用的施加可使污泥固体有效破解,污泥细胞内的活性有机物被释放至水相并形成溶解性有机物,表现为SCODCr的显著增加;采用低频、高比能耗及延长作用时间有利于获取高的SCODCr增加值;污泥在频率25kHz、比能耗2.0W/mL、作用时间30min条件下破解,其厌氧消化累计产气量可从破解前的268mL提高到473mL,相应TCODCr去除率、VS去除率分别从39.1%、33.5%提高至54.3%、61.7%。研究结果表明采用超声破解技术提高污泥的厌氧消化性是可行的。     

电解氧化处理难降解垃圾渗滤液研究

采用连续式电解槽对垃圾渗滤液进行电解催化处理,考察极板间距、电流密度、电导率[Cl-]浓度对电解效果的影响.结果表明,当添加的[Cl-]6000 mg/L,在电解60 min时,对初始COD小于3000 mg/L的中等浓度渗滤液有较好的处理效果,COD和NH3-N的去除率分别达88.9%和97.3%,能耗为2.75 kwh/m3.为中试和工业设计应用提供了参考.     

A study on emission of phthalate esters from plastic materials using a passive flux sampler

Phthalate esters are used as plasticizer in many plastics, and several studies have shown their toxicity. Phthalate esters are gradually emitted over time, and so it is conceivable that they pose a significant health risk. This study aims to investigate the temperature dependence of the emissions of various phthalate esters and to estimate the health risks of these emissions at various temperatures. A passive-type sampler was developed to measure the flux of phthalate esters from the surface of plastic materials. With this sampler, we examined three widely used plastic materials: synthetic leather, wallpaper and vinyl flooring. The observed maximum emissions of diethyl phthalate, dibutyl phthalate, and diethylhexyl phthalate (DEHP) from these materials at 20°C were 0.89, 0.77, and 14 μg m⁻² h⁻¹, respectively. Emissions at 80°C were 2.8, 4.5×10², and 1.5×10³ μg m⁻² h⁻¹, respectively. The results showed this temperature dependence is determined primarily by the type of phthalate ester and less so by the type of material. The estimation from the results of temperature dependence indicated the concentration of DEHP in a vehicle left out in the sunshine during the day can exceed the recommended levels of Japan Ministry of Health, Labour and Welfare.