Prediction of polychlorinated dibenzofuran congener distribution from gas-phase phenol condensation pathways

A model for predicting the distribution of dibenzofuran and polychlorinated dibenzofuran (PCDF) congeners from a distribution of phenols was developed. The model is based on a simplified chemical mechanism. Relative rate constants and reaction order with respect to phenol precursors were derived from experimental results using single phenols and equal molar mixtures of up to four phenols. For validation, experiments were performed at three temperatures using a distribution of phenol and 19 chlorinated phenols as measured in municipal waste incinerator exhaust gas. Comparison of experimental measurements and model predictions for PCDF isomer distributions and homologue pattern shows agreement within measurement uncertainty. The R-squared correlation coefficient exceeds 0.9 for all PCDF isomer distributions and the distribution of PCDF homologues. These results demonstrate that the distribution of dibenzofuran and the 135 PCDF congeners from gas-phase condensation of phenol and chlorinated phenols can be predicted from measurement of the distribution of phenol and the 19 chlorinated phenol congeners.     

Controlled release, blind test of DNAPL remediation by ethanol flushing

A dense nonaqueous phase liquid (DNAPL) source zone was established within a sheet-pile isolated cell through a controlled release of perchloroethylene (PCE) to evaluate DNAPL remediation by in-situ cosolvent flushing. Ethanol was used as the cosolvent, and the main remedial mechanism was enhanced dissolution based on the phase behavior of the water-ethanol-PCE system. Based on the knowledge of the actual PCE volume introduced into the cell, it was estimated that 83 L of PCE were present at the start of the test. Over a 40-day period, 64% of the PCE was removed by flushing the cell with an alcohol solution of approximately 70% ethanol and 30% water. High removal efficiencies at the end of the test indicated that more PCE could have been removed had it been possible to continue the demonstration. The ethanol solution extracted from the cell was recycled during the test using activated carbon and air stripping treatment. Both of these treatment processes were successful in removing PCE for recycling purposes, with minimal impact on the ethanol content in the treated fluids. Results from pre- and post-flushing partitioning tracer tests overestimated the treatment performance. However, both of these tracer tests missed significant amounts of the PCE present, likely due to inaccessibility of the PCE. The tracer results suggest that some PCE was inaccessible to the ethanol solution which led to the inefficient PCE removal rates observed. The flux-averaged aqueous PCE concentrations measured in the post-flushing tracer test were reduced by a factor of 3 to 4 in the extraction wells that showed the highest PCE removal compared to those concentrations in the pre-flushing tracer test.     

农药污染地下水的微生物治理及含水层渗透性变化研究

采用了从农药厂阿特拉津生产车间排污口污泥中分离出的菌种AT菌 ,进行了农药阿特拉津污染地下水微生物治理的模拟实验研究 ,在实验条件 (T =10℃ ,pH =7.5 )与野外含水层的条件基本一致情况下 ,难于生物降解的污染质阿特拉津的一次投菌降解率可达 3 1.0 8% ;设计了两种有效细菌的投放方式以模拟野外条件下的菌种投加条件。另外 ,AT菌的作用会造成被治理含水层的渗透性能降低 ,两种投菌方式下 ,实验后含水层的渗透系数分别下降 60 .5 4%和 3 4 5 6%。清水冲洗 10d的渗透性恢复率分别为 48.96%及 81.3 6% ,说明清水渗透恢复的方法效果明显     

混凝-生物接触氧化法处理城市污水的研究

采用混凝-生物接触氧化法处理生活小区废水,考察了不同混凝剂用量对COD、NH4-N、SS、TP的去除效果,同时研究了生物接触氧化法对COD、NH4-N等的去除以及耐冲击负荷能力.结果表明,随混凝剂用量的增加,COD、SS、TP的去除率随之增加,生物接触氧化法具有较高的抗冲击负荷能力,最大NH4-N去除负荷达到0.55 kg/(m3·d),最大有机去除负荷达到4.32 kg/(m3·d)     

Ligand exchange rate of metal-nom complexes by EDTA

Metal complexation by natural ligands is important for metal transport and distribution in surface and ground water. The goal of the work was to study the ligand exchange rate for two important metal ions in natural aquatic systems (Al, Fe) was determined using EDTA and natural organic matter (NOM) of humic type as ligands. After adding EDTA to a solution containing metal-NOM complexes, these complexes dissociated and metal-EDTA complexes were formed. Metal-NOM complexes were separated from metal-EDTA complexes with the help of size-exclusion chromatography and detected by on-line inductively coupled plasma-mass spectrometry (ICP-MS). Injecting the samples into the system over time after addition of EDTA allowed us to measure the rate of the exchange of NOM by EDTA. The experiments could be well described with a first-order rate law assuming that the dissociation of the metal-NOM complexes is the rate-determining step. The exchange rate of Fe was found to be faster than that of Al. This corresponds well with the exchange rate of water molecules from the coordination sphere of the metal ions, which is also faster for Fe than for Al. Furthermore, the UV and the fluorescence signal of the chromatograms were measured. The results indicate that no disaggregation of NOM molecules took place, although about 75-85% of the aggregate-forming metal ions exchanged NOM by EDTA in their coordination sphere. This suggests clearly the fundamental role of NOM in colloidal transport of metals and in their bioavailability.     

Volatile metabolites from indoor molds grown on media containing wood constituents

Since volatile mold metabolites are used for the detection of mold growth in buildings, it was interesting to determine whether different indoor mold species show different affinity for the major components of wood, a common building material. Growth and volatile metabolites were studied when Aspergillus versicolor, Penicillium chrysogenum, and P. palitans were grown on laboratory substrates containing the major wood constituents cellulose, xylan and lignin. Microbial volatile organic compounds (MVOCs) were characterized by thermal desorption/gas chromatography/mass spectroscopy. Growth and volatile metabolites varied considerably and there appeared to be complementary substrate specificities for P. chrysogenum, and P. palitans grown on cellulose and xylan. The failure of A. versicolor to produce characteristic MVOCs when grown on media containing wood constituents suggests that systems using volatile metabolites to detect microbial growth in buildings may be fundamentally unreliable for the detection of this species.     

生态农业园区废弃物资源化处理利用研究

本文介绍了蟹岛生态园区农业废气物及生活污水的资源化处理工艺方案 ,通过对沼气池和生活污水厌氧 -好氧 -生态塘处理系统进行综合设计 ,实现了节能环保和废弃物无害化综合处理利用。形成了种植业、养殖业、肥料加工、能源利用和休闲度假有机结合的生态农业经济 ,为实现农村经济可持续发展提供了一种新模式     

有机负荷和溶解氧的变化对SBR污泥膨胀的影响及控制方法

本文研究SBR工艺处理汽车电泳废水在不同有机负荷、溶解氧条件下污泥膨胀的现象 ,分析膨胀发生机理 ,分别提出控制方法。实验结果表明 ,在低、中、高负荷时 ,只要溶解氧发生变化 ,均有可能发生膨胀。低负荷、正常溶解氧时发生的膨胀可以通过前联好氧生物选择器加以控制 ;中负荷、低溶解氧及高负荷、低溶解氧活性污泥发生膨胀时可以通过强化曝气得到控制     

车内空气中挥发性有机物的研究

采用热脱附-气相色谱/质谱联用法对4辆处于静止状态下的车辆内部空气中挥发性有机物（VOCs）进行了研究,共定性检出了48种有机物,其中C6～C9之间的组分较多;并对VOCs的总浓度进行了定量,1#～4#车分别为1846、2289、1104和3146 μg/m^3;其中BTEX占VOCs总量的20%～30%;车内VOCs浓度与温度及车辆使用年限密切相关.     

二氧化氯销毁氰化物的应用研究

在弱碱性条件下,二氧化氯消毒剂将氰化物氧化成无毒的氰酸盐(OCN-)、二氧化碳和氮气.研究了影响二氧化氯销毁氰化物的几种因素:pH在8～11的范围内,不影响二氧化氯对氰化物的销毁率;在所试验的反应温度(0～40℃)内,温度对反应速率表现出有限的影响;二氧化氯与氰离子的最佳质量比为2:1;当氰离子最高使用浓度小于0.5 g/L时,废水中氰离子浓度达一级以上的排放标准.