兰州市交通要道颗粒物污染状况及其致突变活性的研究

采用现场监测，色－质联用分析以及小鼠骨髓微核试验方法，评价了兰州市交通要道颗粒物的污染状况，分析了颗粒提取物（PE）的有机组成及致突变活性。结果表明，兰州市总悬浮颗粒物（TSP）污染严重。颗粒提取物中含有近100种有机化合物，其中包括致癌性多环芳烃。微核试验显示PE具有致突变活性，对人群健康的影响不容忽视。     

烟囱颗粒污染物连续监测技术

介绍了一种烟囱颗粒物排放的实时监测装置。该装置基于光散射理论 ,使用一个半导体激光器件作为光源 ,用 4个光电元件分别测定入射光强、从测量区出射的光强及前向两个立体角的散射光能 ,使用一台微机对接收信号进行处理 ,能够实时地给出烟囱排放源的排放浓度及粒径分布。     

Characteristics of air particulate matter and their sources inurban and rural area of Beijing, China

ＩｎｔｒｏｄｕｃｔｉｏｎＴｈｅｒｅｉｓａｇｒｏｗｉｎｇａｗａｒｅｎｅｓｓｔｏｔｈｅｉｍｐｏｒｔａｎｃｅｏｆａｉｒｐｏｌｌｕｔｉｏｎｉｎｍａｊｏｒｃｉｔｅｓ.Ａｎｕｍｂｅｒｏｆｓｔｕｄｉｅｓｈａｖｅｓｈｏｗｎｔｈａｔｔｈｅｃｏｎｃｅｎｔｒａｔｉｏｎｓｏｆｃｅｒｔａｉｎｔｒａｃｅｅｌｅｍｅｎｔｓｉｎｔｈｅｕｒｂａｎａｔｍｏｓｐｈｅｒｅｈａｖｅｂｅｅｎｅｌｅｖａｔｅｄｂｙ ｐｏｌｌｕｔｉｏｎ ,ａｎｄｔｈｅｒｅｆｏｒｅ ,ｔｈｅｈｉｇｈｅｓｔｃｏｎｃｅｎｔｒａｔｉｏｎｓｏｆｔｈｅｓｅｃｈｅｍｉｃａｌｃｏｎｔ…     

淮南市采煤塌陷区水域的有机物污染研究

通过对淮南市采煤塌陷区水域理化指标和叶绿素的测定。用较为简单的W分级法对9个监测点的水质进行评分分级,并对塌陷区水域营养化程度进行了评级,用以反映采煤塌陷区的有机物污染状况。     

水中天然有机物的臭氧强化光催化降解研究

研究了饮用水源中大分子天然有机物（NOM）的臭氧强化光催化降解,考察了臭氧投加量、反应时间和HCO3^-浓度对NOM降解速率的影响;分析了臭氧强化光催化过程中NOM相对分子质量的变化,并比较不同相对分子质量大小NOM的降解速率.研究结果表明,臭氧强化光催化比单独臭氧氧化、光催化能更有效地降解NOM,同时增加臭氧投加量和反应时间才能有效提高臭氧强化光催化对TOC的去除率,而单独增加臭氧投加量可显著提高生物可降解性;HCO3^-显著降低光催化的降解效果,臭氧强化光催化能有效地减弱HCO3^-的不利影响;臭氧强化光催化过程中大分子NOM分解为小分子,SUVA值迅速下降,且相对分子质量越大矿化速度越快.     

Sorption of dissolved organic matter and its effects on the atrazine sorption on soils

IntroductionApplication of organic amendments, such as sewagesludge to agricultural soils, has been considered as aneffective way to improve the soil physico chemical propertiesand organic matter compositions. Dissolved organic matter(D…     

西湖底泥不同供氧条件下有机质降解及CO2与CH4释放速率的模拟研究

采用密闭培养实验装置于室温（２５℃左右）及ｐＨ为７５条件下，对西湖底泥中有机质完全降解及转化为ＣＯ２和ＣＨ４的速率进行了模拟研究．结果表明，在西湖湖水现有供氧水平（５０—８６ｍｇ（Ｏ２）／Ｌ）条件下，底泥中有机质完全降解的速率最为缓慢，培养期间（４２天）平均只有０７２ｍｇ（Ｃ）／（ｋｇ·ｄ）．当湖水供氧水平进一步上升（８６→１２０→１６０ｍｇ（Ｏ２）／Ｌ），ＣＯ２释放速率增加，最大值可达到８７ｍｇ（Ｃ）／（ｋｇ·周）；当湖水供氧水平下降（８６→０ｍｇ（Ｏ２）／Ｌ），ＣＨ４释放速率加快，最大值可达到４６ｍｇ（Ｃ）／（ｋｇ·周）．     

序列间歇式好氧活性污泥法处理生物制药废水研究

本研究采用好氧ＳＢＲ法处理生物制药废水。试验结果表明，废水中不需另加氮磷营养物质，当进水ＣＯＤＣｒ为９１１～３２８０ｍｇ／Ｌ时，在曝气１６ｈ条件下，出水ＣＯＤＣｒ在３５０ｍｇ／Ｌ以下，ＢＯＤ５在８０ｍｇ／Ｌ以下，ＳＳ在１５０ｍｇ／Ｌ以下，皆达到生物制药工业废水二级排放标准。本文还对好氧ＳＢＲ法的有机物降解动力学过程进行了研究。     

Effect of catalyzed diesel particulate filter and its catalyst loading on emission characteristics of a non-road diesel engine

In this study, the effects of a diesel oxidation catalyst (DOC) coupled with a catalyzed diesel particulate filter (CDPF) with different catalyst loadings on the power, fuel consumption, gaseous and particulate emissions from a non-road diesel engine were investigated. Results showed that the after-treatment had a negligible effect on the power and fuel consumption. The reduction effect of the DOC on the CO and hydrocarbon (HC) increased with the engine load. Further reductions occurred coupling with the CDPF. Increasing the catalyst loading resulted in a more significant reduction in the HC emissions than CO emissions. The DOC could increase the NO₂ proportion to 37.9%, and more NO₂ was produced when coupled with the CDPF below 250°C; above 250°C, more NO₂ was consumed. The after-treatment could reduce more than 99% of the particle number (PN) and 98% of the particle mass (PM). Further reductions in the PN and PM occurred with a higher CDPF catalyst loading. The DOC had a better reduction effect on the nucleation particles than the accumulation ones, but the trend reversed with the CDPF. The DOC shifted the particle size distribution (PSD) to larger particles with an accumulation particle proportion increasing from 13% to 20%, and the geometric mean diameter (GMD) increased from 18.2 to 26.0 nm. The trend reversed with the CDPF and the accumulation particle proportion declined to less than 10%. A lower catalyst loading on the CDPF led to a higher proportion of nucleation particles and a smaller GMD.     

Comparison of UV-based advanced oxidation processes for the removal of different fractions of NOM from drinking water

This study examined the effectiveness for degradation of hydrophobic (HPO), transphilic (TPI) and hydrophilic (HPI) fractions of natural organic matter (NOM) during UV/H₂O₂, UV/TiO₂ and UV/K₂S₂O₈ (UV/PS) advanced oxidation processes (AOPs). The changing characteristics of NOM were evaluated by dissolved organic carbon (DOC), the specific UV absorbance (SUVA), trihalomethanes formation potential (THMFP), organic halogen adsorbable on activated carbon formation potential (AOXFP) and parallel factor analysis of excitation–emission matrices (PARAFAC-EEMs). In the three UV-based AOPs, HPI fraction with low molecular weight and aromaticity was more likely to degradate than HPO and TPI, and the removal efficiency of SUVA for HPO was much higher than TPI and HPI fraction. In terms of the specific THMFP of HPO, TPI and HPI, a reduction was achieved in the UV/H₂O₂ process, and the higest removal rate even reached to 83%. UV/TiO₂ and UV/PS processes can only decrease the specific THMFP of HPI. The specific AOXFP of HPO, TPI and HPI fractions were all able to be degraded by the three UV-based AOPs, and HPO content is more susceptible to decompose than TPI and HPI content. UV/H₂O₂ was found to be the most effective treatment for the removal of THMFP and AOXFP under given conditions. C1 (microbial or marine derived humic-like substances), C2 (terrestrially derived humic-like substances) and C3 (tryptophan-like proteins) fluorescent components of HPO fraction were fairly labile across the UV-based AOPs treatment. C3 of each fraction of NOM was the most resistant to degrade upon the UV-based AOPs. Results from this study may provide the prediction about the consequence of UV-based AOPs for the degradation of different fractions of NOM with varied characteristics.