剩余污泥氮磷营养盐提取方法研究

为提取污泥中的氮磷营养盐,以实现污泥的资源化和减量化,分别采用热碱法、超声波法和加碱超声波法对剩余污泥进行处理.在优化提取工艺条件的基础上,比较了3种方法对污泥中无机氮(IN)和磷酸盐(PO34--P)的提取效果以及污泥减量效果.结果表明,热碱法的适宜提取条件为pH=13、T=100℃、t=9 h;超声波法的适宜提取条...     

A spectrophotometric method for detection of enzymatic degradation of thin polymer films

An assay method has been developed for monitoring the enzymatic degradation of thin films of translucent polymers. The method was based on the observation that when a solution-cast film of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) was exposed to a solution of a depolymerase fromPseudomonas lemoignei, the surface of the film roughened and the film became visibly turbid. This increase in turbidity could be measured spectrophotometrically and was reproducible during the initial stage of degradation. Turbidity correlated very closely with film weight loss early in the degradation but reached a maximum value before extensive degradation had taken place. For a given set of films, this correlation was independent of the concentration of the enzyme used, although it did vary with the mode of enzyme exposure. The turbidity was associated with the exposure of crystalline domains due to the removal of amorphous material from the film surface. The increase in crystallinity at the surface was verified by attenuated total reflectance infrared spectroscopy (ATRIR). In conjunction with SEM, weight loss, and ATRIR, the film turbidity assay provided much semiquantitative insight into the mechanism of the enzymatic degradation reaction. This assay was used to study the enzymatic degradation of films of PHBV solution blended with cellulose acetate esters (CAE). The presence of only 25% of CAE of degree of substitution 2.9 severely hampered the enzymatic degradability of PHBV, a result which is consistent with the environmental degradation of these same samples exposed to activated sludge.     

Biotic and abiotic transformations of methyl tertiary butyl ether (MTBE)

Background Methyl tertiary butyl ether (MTBE) is a fuel additive which is used all over the world. In recent years it has often been found in groundwater, mainly in the USA, but also in Europe. Although MTBE seems to be a minor toxic, it affects the taste and odour of water at concentrations of < 30 μg/L. Although MTBE is often a recalcitrant compound, it is known that many ethers can be degraded by abiotic means. The aim of this study was to examine biotic and abiotic transformations of MTBE with respect to the particular conditions of a contaminated site (former refinery) in Leuna, Germany. Methods Groundwater samples from wells of a contaminated site were used for aerobic and anaerobic degradation experiments. The abiotic degradation experiment (hydrolysis) was conducted employing an ion-exchange resin and MTBE solutions in distilled water. MTBE, tertiary butyl formate (TBF) and tertiary butyl alcohol (TBA) were measured by a gas chromatograph with flame ionisation detector (FID). Aldehydes and organic acids were respectively analysed by a gas chromatograph with electron capture detector (ECD) and high-performance ion chromatography (HPIC). Results and Discussion Under aerobic conditions, MTBE was degraded in laboratory experiments. Only 4 of a total of 30 anaerobic experiments exhibited degradation, and the process was very slow. In no cases were metabolites detected, but a few degradation products (TBF, TBA and formic acid) were found on the site, possibly due to the lower temperatures in groundwater. The abiotic degradation of MTBE with an ion-exchange resin as a catalyst at pH 3.5 was much faster than hydrolysis in diluted hydrochloric acid (pH 1.0). Conclusion Although the aerobic degradation of MTBE in the environment seems to be possible, the specific conditions responsible are widely unknown. Successful aerobic degradation only seems to take place if there is a lack of other utilisable compounds. However, MTBE is often accompanied by other fuel compounds on contaminated sites and anaerobic conditions prevail. MTBE is often recalcitrant under anaerobic conditions, at least in the presence of other carbon sources. The abiotic hydrolysis of MTBE seems to be of secondary importance (on site), but it might be possible to enhance it with catalysts. Recommendation and Outlook MTBE only seems to be recalcitrant under particular conditions. In some cases, the degradation of MTBE on contaminated sites could be supported by oxygen. Enhanced hydrolysis could also be an alternative. - * The basis of this peer-reviewed paper is a presentation at the 9th FECS Conference on 'Chemistry and Environment', 29 August to 1 September 2004, Bordeaux, France.     

水胺硫磷工业废水的酸性水解处理研究

水胺硫磷工业废水中 ,有机磷和硫化物含量均 >10 0 0 0mg/L ,COD高达 5 5 0 0 0mg/L左右 ,NH3 N在 4 0 0 0 0mg/L左右 ,BOD/COD仅为 0 .0 5 ,属典型难生物降解废水。本文采用常压酸性水解和脱氨除磷工艺处理该废水 ,有机磷、硫化物、NH3 N和总磷等去除率均 >90 % ,COD去除率达到 5 0 %以上 ,废水可生化性提高 ;同时 ,可回收得到硫氢化钠、氨水等物质 ,使废水资源得到了综合利用     

高原喀斯特土壤有机碳短期稳定的温度作用机制

探明有机碳稳定的温度作用机制,是评估全球变化背景下土壤碳源/汇演变趋势的关键.应用土壤密度分组和酸水解技术,采用红外线辐射增温法,对比研究不同升温情景下高原喀斯特土壤及其物理和生化组分中有机碳密度的短期(4a)变化特征.升温情景包括不升温(对照)、对称升温(全年同步升温2.0℃)和非对称升温(冬春/夏秋季升温幅度为2.5℃/1.5℃、3.0℃/1.0℃、3.5℃/0.5℃和4.0℃/0℃,低度、中度、高度和极端非对称升温),其中中度非对称升温与该区域多年升温情景类似.结果表明,不同升温情景下表层(0~15 cm)土壤有机碳密度在1.95~2.02 kg·m-2之间,其差异不显著,且与对照(1.94 kg·m-2)差异不显著.升温处理间土壤轻组和重组碳密度、重组顽固性碳密度差异不显著,且与对照差异不显著.5个升温处理轻组顽固性碳平均密度是对照的1.18倍,其中对称升温、低度和中度非对称升温处理显著高于对照.轻组顽固性碳密度和轻组顽固性碳指数随升温的非对称性增加而降低,其中对称升温处理均显著高于中度、高度和极端非对称升温.亚表层(15~30 cm)土壤及其物理和生化组分中有机碳密度对短期升温均不敏感.研究揭示:短期内,升温提高了高原喀斯特土壤非保护组分中有机碳顽固性.基于对称升温情景并不一定会误估全球变暖对土壤有机碳数量和土壤碳物理保护能力的影响,但可能会高估表层土壤(0~15 cm)非保护组分有机碳顽固性.     

污水中基于酶活性分析的硫酸雌酮雌激素效应

在污水处理厂尾水中,雌酮（E1）和硫酸雌酮（E1-3-S）分别是赋存浓度最高的自由态雌激素和结合态雌激素.E1-3-S难以被生物降解且雌激素效应有限,但环境条件适宜时可在芳基硫酸酯酶（AryS）作用下通过水解释放出具有雌激素效应的E1.本论文提出了一种利用AryS活性值和E1-3-S酶促水解动力学参数计算E1-3-S半寿期的方法.根据现场取样分析得到了重庆市某污水处理厂生物处理构筑物内混合液,合流制管道溢流口与尾水受纳水体底泥中在冬、春、夏3个季节的AryS活性值,其均值分别为417.41~941.14,91.55~179.42,28.11~59.64μg对硝基酚/（g·h）.在20℃的实验室条件下,E1-3-S的酶促水解遵循一级动力学模式（P<0.01）,且水解速率K_d与AryS活性呈线性正相关（R²=0.9774）.根据春季的AryS活性数据和实验室条件下E1-3-S水解速率与酶活性的线性回归方程推算,得到了在污水处理厂生物构筑物内、合流制管网溢流口和污水厂尾水排放点附近水体中E1-3-S在对应环境温度条件下通过酶促水解的半寿期分别为33.5,153.0,410.0h.该方法可用于评估硫酸型结合态雌激素在水环境中的雌激素效应释放风险.     

挺水植物生物炭对硫丹的吸附及催化水解作用

以美人蕉、菖蒲、芦苇、茭白、再力花、芦竹等挺水植物为原料,在限氧升温（550℃）条件下制备6种不同性质的生物炭,研究其组成及结构对硫丹吸附和催化水解作用.结果表明：550℃下热解,湿地植物生物炭所含灰分高于一般农产品废弃物,介于10.88%~31.11%间.生物炭表面芳香类官能团较多,孔隙部分呈碎片化,以介孔为主.6种生物炭对硫丹都具良好吸附性能.吸附行为主要发生在含致密有机质的生物炭表面,包括疏水、扩散及分配作用等.中/碱性条件下,美人蕉生物炭、菖蒲生物炭及再力花生物炭能有效去除水溶液中的硫丹,去除率为96.77%~98.57%.中性条件下,因生物炭对硫丹的催化,对硫丹的去除率提高约16.57%~72.57%.     

Physical properties and biodegradability of blends containing poly(ε-caprolactone) and tropical starches

In order to assess feasibility of tropical starches (sago and cassava starches) as biodegradable plastic materials, blending with poly(-caprolactone) (PCL), a biodegradable polymer, was carried out. It was confirmed that the physical properties (tensile strength and elongation) of PCL/sago and PCL/cassava blends were similar to those of PCL/corn blend, suggesting that sago and cassava starches can also be blended with PCL for production of biodegradable plastic. However, the properties of all PCL/starch blends were still low compared with those of polyethylene. Enzymatic degradability evaluation showed that lipase degradation of PCL and-amylase degradation of starch increased as the starch content in the blend increased. Burial test of the blends for 1, 3, and 5 months was carried out and the rate of degradation of the PCL/sago blend was confirmed to be slower than those of PCL/corn and PCL/cassava blends. Observation of the film blends structure by scanning electron microscope revealed that the starch was dispersed in a PCL continuous phase. Furthermore, changes in the film surface before and after enyzme treatments were observed.     

水解酸化-缺氧法处理采油废水的污染物迁移降解试验研究

水解酸化-缺氧法对采油废水有较好的处理效果,采用GC/MS技术对水解酸化-缺氧法处理采油废水过程中污染物的迁移降解进行的研究表明:水解酸化段和缺氧段对采油废水中碳原子为C6～C9、分子量为100～140的有机物均有较好的降解能力.其中,在水解酸化段中酮类、芳烃得到较好的降解,缺氧段中酚类和醚类化合物降解明显.水解酸化-缺氧工艺对于采油废水中的甲苯和二甲苯具有较好的降解能力.     

气浮-水解-序批式活性污泥法处理高浓度特种丙烯酸废水

采用气浮—水解—序批式活性污泥法(SBR)处理高浓度特种丙烯酸废水,研究了投加生活污水对处理效果的影响及厌氧水解时间、SBR曝气时间、污泥负荷等因素对COD去除率的影响,结果表明,按1∶1体积比投加生活污水,厌氧水解时间2d,序批式活性污泥法曝气时间10h(进水后期曝气1h,共曝气11h),污泥负荷小于或等于0.08kg/(kg.d)时,出水COD小于85m g/L,满足处理要求。