Degradation and plant uptake of nonylphenol (NP) and nonylphenol-12-ethoxylate (NP12EO) in four contrasting agricultural soils

Nonylphenol polyethoxylates (NPEOs) are surfactants found ubiquitously in the environment due to widespread industrial and domestic use. Biodegradation of NPEOs produces nonylphenol (NP), an endocrine disruptor. Sewage sludge application introduces NPEOs and NP into soils, potentially leading to accumulation in soils and crops. We examined degradation of NP and nonylphenol-12-ethoxylate (NP12EO) in four soils. NP12EO degraded rapidly (initial half time 0.3-5 days). Concentrations became undetectable within 70-90 days, with a small increase in NP concentrations after 30 days. NP initially degraded quickly (mean half time 11.5 days), but in three soils a recalcitrant fraction of 26-35% remained: the non-degrading fraction may consist of branched isomers, resistant to biodegradation. Uptake of NP by bean plants was also examined. Mean bioconcentration factors for shoots and seeds were 0.71 and 0.58, respectively. Removal of NP from the soil by plant uptake was negligible (0.01-0.02% of initial NP). Root concentrations were substantially higher than shoot and seed concentrations.     

微波萃取技术在分析土壤中有机污染物的应用

介绍了微波萃取技术及其使用的试剂、设备和条件,对微波萃取在分析土壤中有机污染物的应用予以综述,阐述了微波萃取技术是分析土壤中有机污染物的好方法。     

Accumulation of Heavy Metals in Epiphytic Lichens Near a Municipal Solid Waste Incinerator (Central Italy)

The epiphytic lichen Parmelia caperata was usedas biomonitor in the area of a municipal solid wasteincinerator (Poggibonsi, central Italy) to investigatethe levels and the spatial distribution of the heavymetals Al, Cd, Cr, Cu, Fe, Hg, Pb and Zn. Levels ofAl, Cu and Hg were similar to those in unpollutedareas, whereas high values were found for Cr, Zn andespecially Cd. The distribution pattern of the lastthree metals and the exponential relationship of theirconcentrations with distance from the incinerator,showed that the disposal plant is a local source ofatmospheric pollution due to Cd, Cr and Zn. For thesemetals, long-term hazard should be seriously taken into account.     

高浓度洗毛废水生物降解的研究

根据高浓度洗毛废水的水质特性,选择、驯化出高效污泥和菌株,并对生物降解该废水时的工艺、污泥量、时间三要素进行了深入的研究．结果表明,对于物化处理彻底的废水, Ｈ／ Ｏ 工艺（ 水解／ 好氧工艺） 与好氧工艺处理差异不大;７０ ％ 左右物化效果时, Ｈ／ Ｏ 工艺处理时, Ｃ Ｏ Ｄｃｒ 去除率增加;废水在处理过程中成分变化大,后段水可用筛选优势菌的方法处理．实验室流动模型运行结果为：在原水ρ（ Ｃ Ｏ Ｄｃｒ） １８５４４ ｍｇ／ Ｌ 和设定ｔ Ｈ Ｒ（ 延滞期） 下,混凝后出水ρ（ Ｃ Ｏ Ｄｃｒ） ５３２２ ｍｇ／ Ｌ,水解池出水ρ（ Ｃ Ｏ Ｄｃｒ） ４７６３ ｍｇ／ Ｌ,好氧池出水 Ｃ Ｏ Ｄｃｒ１９９ ．９ ｍｇ／ Ｌ,总 Ｃ Ｏ Ｄｃｒ去除率为９８ ．９ ％     

邯郸市沁河水污染治理方案

本文对邯郸市沁河水污染现状进行了调查分析,总结了城市内河治理经验,通过方案比较,推荐“清淤,护坡,建坝,分质截污,邯钢废水混凝沉淀处理”为沁河治理方案。     

城市生活垃圾焚烧处理过程中重金属迁移规律研究

通过采集厦门2个垃圾焚烧发电厂进厂垃圾、渗滤液、飞灰、炉渣和烟气样品,分析垃圾组成成分及各组分的重金属含量,结果表明,垃圾中以厨余、橡塑类和纸类为主,共占到垃圾干基的78．08％,重金属含量大小次序为Zn〉Cu〉Pb〉Cr〉Ni〉Cd〉Hg;垃圾渗滤液中除Zn外,其他金属的含量都较低,一厂渗滤液中重金属Ni、Zn迁移量较大,分别达到24．46％和8．52％。二厂渗滤液中重金属的迁移有相同的趋势,但含量相对较高。垃圾焚烧后其重金属主要分布在飞灰和废渣中,烟气中的含量非常少,不同金属的含量均有差别,这与金属的性质有很大关系;通过浸出毒性分析,飞灰中重金属酸溶态含量多,容易浸出,属于危险废物。同时,不同烟气处理工艺产生的飞灰的重金属浸出量有很大差别。     

Extraction of raw sewage sludge containing iron phosphate for phosphorus recovery

The objective of the present study was to establish an alkali extraction technology for FePO₄-containing sewage sludge obtained from a wastewater treatment system that includes phosphorous removal by iron electrolysis. By clarifying the extraction properties of phosphorous, organic matter, and inorganic matter, conditions for alkali extraction were optimized. As a result, it was suggested that unheated phosphorous extraction would be superior for FePO₄-containing sewage sludge. And, extraction methods and sewage sludge properties were also compared, and the noteworthy result that extraction of metals can be suppressed to extremely low amounts with alkali extraction as compared with acid extraction was obtained. A new insight was also gained that, as compared with the use of incinerated ash reported in previous studies, alkali extraction was more efficient when raw sewage sludge was used.     

不同粒径零价铁（ZVI）对污水污泥H_2S和CH_4释放速率的影响

考察了不同粒径零价铁（ZVI）,包括200目普通铁粉（200m-ZVI）、800目超细铁粉（800m-ZVI）和纳米铁粉（nZVI,粒径=20 nm）,对污水污泥的硫化氢和甲烷释放速率的影响。研究发现：（1）在22 d内,添加0.1%的200m-ZVI使污泥的硫化氢释放速率提高48.0%,而添加0.1%的800-ZVI和nZVI,则使污泥的硫化氢释放速率分别降低33.1%和77.1%;（2）不同粒径ZVI均可以提高污泥沼气中的甲烷浓度,且依次为nZVI〉800m-ZVI〉200m-ZVI;（3）在23 d内,添加0.1%的200m-ZVI和nZVI使污泥的甲烷累计产生量分别提高了15.5%和40.6%,而添加0.1%800m-ZVI则使甲烷产生量降低了12.5%。nZVI可以有效控制污泥的硫化氢释放,并显著提升污泥在厌氧发酵过程的产甲烷速率。     

红斑顠体虫的污泥减量效果

为了实现红斑顠体虫捕食污泥减量化,对不同条件下红斑顠体虫的污泥减量效果进行实验研究。实验结果表明：红斑顠体虫的污泥减量速率随初始MLSS及温度的增大而增大,初始MLSS越高,污泥减量速率越大。污泥减量速率随红斑顠体虫密度变化率的增大而逐渐增大,当红斑顠体虫的密度增长率出现下降时,污泥减量速率也呈下降趋势。采用间歇曝气（12 h曝气,12 h停曝）方式,红斑顠体虫的污泥减量速率会显著下降。在污泥好氧消化时,红斑顠体虫能捕食污泥中的有机碎片和细菌,达到污泥稳定化的指标要求。     

Fate of ah receptor agonists during biological treatment of an industrial sludge containing explosives and pharmaceutical residues

GOAL, SCOPE AND BACKGROUND: Sweden is meeting prohibition for deposition of organic waste from 2005. Since 1 million tons of sludge is produced every year in Sweden and the capacity for incineration does not fill the demands, other methods of sludge management have to be introduced to a higher degree. Two biological treatment alternatives are anaerobic digestion and composting. Different oxygen concentrations result in different microbial degradation pathways and, consequently, in a different quality of the digestion or composting residue, It is therefore necessary to study sludge treatment during different oxygen regimes in order to follow both degradation of compounds and change in toxicity. In this study, an industrial sludge containing explosives and pharmaceutical residues was treated with anaerobic digestion or composting, and the change in toxicity was studied. Nitroaromatic compounds, which are the main ingredients of both pharmaceutical and explosives, are well known to cause cytotoxicity and genotoxicity. However, little data are available concerning sludge with nitroaromatics and any associated dioxin-like activity. Therefore, we studied the sludge before and after the treatments in order to detect any changes in levels of Ah receptor (AhR) agonists using two bioassays for dioxin-like compounds. METHODS: An industrial sludge was treated with anaerobic digestion or composting in small reactors in a semi-continuous manner. The same volume as the feeding volume was taken out daily and stored at -20 degrees C. Sample preparation for the bioassays was done by extraction using organic solvents, followed by clean up with silica gel or sulphuric acid, yielding two fractions. The fractions were dissolved in DMSO and tested in the bioassays. The dioxin-like activity was measured using the DR-CALUX assay with transfected H4IIE rat hepatoma pGudluc cells and an EROD induction assay with RTL-W1 rainbow trout liver cells. RESULTS AND DISCUSSION: The bioassays showed that the sludge contained AhR agonists at levels of TCDD equivalents (TEQs) higher than other sludge types in Sweden. In addition, the TEQ values for the acid resistant fractions increased considerably after anaerobic digestion, resulting in an apparent formation of acid resistant TEQs in the anaerobic reactors. Similar results have been reported from studies of fermented household waste. There was a large difference in effects between the two bioassays, with higher TEQ levels in the RTL-W1 EROD assay than in the DR-CALUX assay. This is possibly due to a more rapid metabolism in rat hepatocytes than in trout hepatocytes or to differences in sensitivities for the AhR agonists in the sludge. It was also demonstrated by GC/FID analysis that the sludge contained high concentrations of nitroaromatics. It is suggested that nitroaromatic metabolites, such as aromatic amines and nitroanilines, are possible candidates for the observed bioassay effects. It was also found that the AhR agonists in the sludge samples were volatile. CONCLUSIONS: The sludge contained fairly high concentrations of volatile AhR agonists. The increase of acid resistant AhR agonist after anaerobic digestion warrants further investigations of the chemical and toxic properties of these compounds and of the mechanisms behind this observation. RECOMMENDATION AND OUTLOOK: This study has pointed out the benefits of using different types of mechanism-specific bioassays when evaluating the change in toxicity by sludge treatment, in which measurement of dioxin-like activity can be a valuable tool. In order to study the recalcitrant properties of the compounds in the sludge using the DR-CALUX assay, the exposure time can be varied between 6 and 24 hours. The properties of the acid-resistant AhR agonists formed in the anaerobic treatment have to be investigated in order to choose the most appropriate method for sludge management.