污泥好氧消化的研究现状及发展趋势

污泥好氧消化是一种有效实用的污泥稳定技术，适用于处理量较小(≤20000m^3／d)的污水处理厂。在分析中，对污泥好氧消化的3种工艺(CAD、A／AD、ATAD)的工艺原理、影响参数及研究现状进行了详细的介绍，并在对国内外文献进行总结的基础上，分析了污泥好氧消化的研究方向与发展趋势。     

超声波预处理对污泥好氧/缺氧消化的效果

为评价超声波预处理对城市污泥好氧/缺氧消化效果的影响,将超声波-好氧/缺氧消化工艺与传统的好氧/缺氧消化工艺进行了对比研究。结果表明,经25 d消化处理,引进超声波后的好氧/缺氧消化效果显著提高,污泥的VSS去除率达到51.98%,高于传统好氧/缺氧消化的42.98%。2种工艺消化的污泥TCOD以及污泥上清液中的SCOD、TP和NH3-N的变化趋势相似;而经超声波-好氧/缺氧消化的污泥上清液中硝态氮和亚硝态氮浓度较传统好氧/缺氧的高,说明经超声波处理后的污泥中的硝化细菌的活性增强,硝化反应加快。     

微生物强化MBR工艺剩余污泥的好氧消化过程

为了考察原位污泥减量技术产生的长污泥龄污泥好氧消化可能性,以某污水处理厂MBR工艺产生的剩余污泥为研究对象(污泥龄为60 d),将实验筛选得到的强化效果最佳的3种菌种(分别为B4、H4和N2)分别投加到MBR剩余污泥好氧消化反应器中。经过58 d的好氧消化后,投加B4、H4和N2的3个反应器MLSS消解率分别比污泥对照提高了13.2%、11.7%和6.2%,其中投加B4菌种MLSS消化效率提高最多。MLVSS消解率分别比污泥对照提高18.8%、20.0%和11.0%。研究表明原位污泥减量技术产生的长污泥龄污泥具有污泥好氧消化的可能性,同时筛选出来的3种菌种在消化过程中有明显的强化效果。随着消化反应的进行到52 d,反应器中出现大量的硝酸盐氮和总磷的积累。观察反应过程中氨氮、硝酸盐氮、p H和总磷的变化,大量的硝酸盐存在时诱导以硝酸盐为电子受体的反硝化除磷的进行。在消化过程中,磷溶出情况取决于污泥的水解程度,投加菌种加速了总磷溶出和提高了污泥的水解程度。同时投加菌种强化好氧消化显著降低污泥的SVI,投加菌种在强化好氧消化过程中能更多地消耗污泥中有机物,进而提高消化效率。     

好氧/缺氧消化降解污泥特征分析

为考察好氧/缺氧消化过程中污泥降解的特征，利用2个反应器进行对比试验，研究好氧/缺氧和好氧消化2个过程中VS的去除，pH和碱度变化，消化上清液中COD和氮元素变化等情况。试验结果表明:好氧/缺氧消化能够满足污泥稳定的要求，在常温条件下，消化16 d VS去除率即可达到38.2%，同时比好氧消化节约曝气能耗。好氧/缺氧消化对污泥中总氮的去除率高于传统的好氧消化，达到了36.4%，而且能够降低消化污泥上清液中的氨氮和硝态氮浓度。     

电化学预处理提高剩余污泥好氧消化性能研究

采用电化学方法对好氧消化处理前的剩余污泥(以下简称污泥)进行预处理,考察了不同预处理条件对污泥有机物(以MLVSS来表征)的去除效果,探讨了电化学预处理对污泥好氧消化效率的影响。结果表明,以网状钛涂钌电极板为电极,在pH为11.00,极板间距为2.0cm,工作电压为15V,气体搅拌作用下电解30min后,污泥(初始质量浓度为20.04g/L)的MLVSS去除率达9.7%。污泥经过电化学预处理后,在自然温度(10～15℃)下进行好氧消化处理,14d后MLVSS去除率达40.1%,而同期未经预处理的污泥MLVSS去除率为33.2%,并于20d后达40.2%。经电化学预处理后污泥的好氧消化效率显著提高,大大缩短了污泥好氧消化的时间。     

中小型污水处理厂污泥的自动升温好氧消化工艺及其应用

城市污水处理厂的污泥需要进行减量化、稳定化、无害化处理，因此介绍了一种适合中小型污水处理厂污泥处理的自动升温好氧消化的新工艺。根据当前国内污泥处理的状况，提出的自动升温好氧消化工艺，是适合中小型污水处理厂污泥处理的，是一项具有发展前景的新技术。     

超声波促进城市生活污泥缺氧/好氧消化的研究

本研究将超声波预处理引入城市生活污泥缺氧/好氧消化工艺中，自主设计了容积为30 L的生活污泥超声波-缺氧/好氧消化中试系统并用以实验研究。超声波预处理的参数为超声频率28 kHz，声能密度0.15 W/mL，超声时间10 min，超声间隔12 h，污泥超声比例30%。结果表明，引入超声预处理后，缩短了污泥的稳定时间，提高了污泥的消化效率。污泥消化10 d就已经达到了稳定标准，比未引入超声预处理时缩短了12 d，而MLVSS最大去除率提高了11%，达到了55.10%。超声波的引入，对污泥缺氧/好氧消化系统中污泥上清液溶解性COD（SCOD）的变化趋势影响比较明显，而对上清液的pH、氨氮和TP的变化趋势没有明显影响。     

微好氧预处理对市政污泥厌氧消化产甲烷的影响

针对目前市政污泥处理资源化与减量化效率低的问题,利用微好氧预处理技术进行预处理,提高其甲烷产量。利用有机物溶出效率、VSS减量、甲烷产量3项指标对预处理效果进行了评价;研究了不同参数条件下微好氧预处理对市政污泥厌氧消化产甲烷的影响;探讨了微好氧预处理对污泥胞外聚合物的影响。结果表明,微好氧预处理可以促进污泥溶解性有机物释放、提高VSS去除率;在最佳反应条件下(曝气强度0.30m3·(min·m3)-1、预处理时间12 h),相对于未经过预处理的工况,甲烷产量可提高26.77%;微好氧预处理对剩余污泥活性细胞的影响主要发生在胞外聚合物部分,同时也存在对活性微生物的破解作用。市政污泥经过微好氧预处理后,可有效提升后续中温厌氧消化或高温厌氧消化的甲烷产量。     

超声波预处理提高污泥好氧消化性能研究

为评价超声波预处理对提高污泥生物消化的作用,采用超声波预处理与好氧消化衔接,测试了污泥消化的溶解性有机物(SCOD)、TSS及蛋白酶变化过程.结果表明,污泥超声波预处理效果较好的能量密度与时间分别为12 kW/L和10 min,此时有机物释放与能量输入之比较优;在此条件下,经预处理后的污泥好氧消化性能明显比未处理的高.消化时间为10.5 d时,经超声波预处理的污泥TSS减量42.7%,而未处理的污泥仅减量20.9%.经超声波预处理后,污泥中的蛋白酶活性明显提高;同时,超声波预处理释放出较多的可溶性物质.因此,增加的可溶性物质与蛋白酶活性使得污泥迅速降解,提高了污泥好氧消化效率,缩短了污泥好氧消化时间.     

电化学预处理污泥的机制研究

采用电化学方法对含固宰为2％(质量分数)的污泥进行预处理.不仅可去除污泥中10.5％的挥发性悬浮固体(VSS),而且还可使后续的污泥好氧消化时间由20 d缩短为16 d.为了探讨电化学预处理提高污泥好氧消化性能的机制,对预处理前后的污泥性质进行了研究,发现污泥经电化学预处理后,上清液中可溶性有机物(SCOD)、TN、T...     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Radionuclides and trace elements in fish collected upstream and downstream of Los Alamos national laboratory and the doses to humans from the consumption of muscle and bone

Abstract

The purpose of this study was to determine radionuclide and trace element concentrations in bottom‐feeding fish (catfish, carp, and suckers) collected from the confluences of some of the major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG) and the potential radiological doses from the ingestion of these fish. Samples of muscle and bone (and viscera in some cases) were analyzed for ³H, ⁹⁰Sr, ¹³⁷Cs, ^totU, ²³⁸Pu, ^239,240Pu, and ²⁴¹Am and Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl. Most radionuclides, with the exception of ⁹⁰Sr, in the muscle plus bone portions of fish collected from LANL canyons/RG were not significantly (p<0.05) higher from fish collected upstream (San Ildefonso/background) of LANL. Strontium‐90 in fish muscle plus bone tissue significantly (p<0.05) increases in concentration starting from Los Alamos Canyon, the most upstream confluence (fish contained 3.4E‐02 pCi g^‐1 [126E‐02 Bq kg^‐1]), to Frijoles Canyon, the most downstream confluence (fish contained 14E‐02 pCi g^‐1 [518E‐02 Bq kg^‐1]). The differences in ⁹⁰Sr concentrations in fish collected downstream and upstream (background) of LANL, however, were very small. Based on the average concentrations (±2SD) of radionuclides in fish tissue from the four LANL confluences, the committed effective dose equivalent from the ingestion of 46 lb (21 kg) (maximum ingestion rate per person per year) of fish muscle plus bone, after the subtraction of background, was 0.1 ± 0.1 mrem y^‐1 (1.0 ± 1.0 μSv y^‐1), and was far below the International Commission on Radiological Protection (all pathway) permissible dose limit of 100 mrem y^‐1 (1000 μSv y^‐1). Of the trace elements that were found above the limits of detection (Ba, Cu, and Hg) in fish muscle collected from the confluences of canyons that cross LANL and the RG, none were in significantly higher (p<0.05) concentrations than in muscle of fish collected from background locations.     

A History of Dry Cleaners and Sources of Solvent Releases from Dry Cleaning Equipment

Approximately 25, 000-35, 000 dry cleaning facilities currently operate in the U.S. The release of perchloroethylene and other solvents from these establishments represents a major source of soil and groundwater contamination. The manner in which dry cleaning solvents escape from dry cleaning plants is, for all practical purposes, identical for chlorinated and petroleum hydrocarbon solvents and is related to one of the following events: the catastrophic failure of a component of the dry cleaning system, the improper installation, operation or maintenance of the dry cleaning equipment or a combination of all of these causes. Acceptable customs, codes and regulations can also dictate what is authorized for operation of a dry cleaning facility in a particular community, geographic area during a particular time frame. Environmental litigation dealing with the origin of a solvent release from dry cleaners tends to focus on the design and manufacture of dry cleaning industry machines such as washers, washer extractors, tumblers, solvent filters, water separators, stills and spotting boards. A thorough analysis of the daily operations of dry cleaners often reveals that poor maintenance, failure to follow the manufacturer's instructions and the actions of the operator are the most likely causes of soil and groundwater pollution. In order to forensically evaluate the most probable origins of a solvent release and to examine issues regarding liability, a thorough understanding of the history of dry cleaning and a detailed analysis of the operation and maintenance of the dry cleaning equipment are necessary. The discovery of solvent plumes in the vicinity of dry cleaning plants may suggest that the solvent source is the dry cleaning plant; however, the presence of these plumes does not necessarily indicate that the dry cleaning equipment was defectively designed or manufactured. A thorough review of the type of equipment used over the life of the dry cleaning plant and verifiable solvent mileage records frequently indicates that operators of the plant have disposed of solvent and contaminated solids into the municipal sewer or on ground surfaces.     

Radionuclides in deer and elk from Los Alamos national laboratory and the doses to humans from the ingestion of muscle and bone

Abstract

This paper summarizes radionuclide concentrations (³H, ⁹⁰Sr, ¹³⁷Cs, ²³⁸Pu, ^239,240Pu, ²⁴¹Am, and ^totU) in muscle and bone tissue of mule deer (Odocoileus hemionus) and Rocky Mountain elk (Cervus elaphus) collected from Los Alamos National Laboratory (LANL), Los Alamos, New Mexico, lands from 1991 through 1998. Also, the committed effective dose equivalent (CEDE) and the risk of excess cancer fatalities (RECF) to people who ingest muscle and bone from deer and elk collected from LANL lands were estimated. Most radionuclide concentrations in muscle and bone from individual deer (n = 11) and elk (n = 22) collected from LANL lands were either at less than detectable quantities (where the analytical result was smaller than two counting uncertainties) and/or within upper (95%) level background (BG) concentrations. As a group, most radionuclides in muscle and bone of deer and elk from LANL lands were not significantly higher (p<0.10) than in similar tissues from deer (n = 3) and elk (n = 7) collected from BG locations. Also, elk that had been radio collared and tracked for two years and spent an average time of 50% on LANL lands were not significantly different in most radionuclides from road kill elk that have been collected as part of the environmental surveillance program. Overall, the upper (95%) level net CEDEs (the CEDE plus two sigma for each radioisotope minus background) at the most conservative ingestion rate (50 lbs of muscle and 13 lbs of bone) were as follows: deer muscle = 0.22 mrem y^‐1 (2.2 μSv y^‐1), deer bone = 3.8 mrem y^‐1 (38 μSv y^‐1), elk muscle = 0.12 mrem y^‐1 (1.2 μSv y^‐1), and elk bone = 1.7 mrem y^‐1 (17 μSv y^‐1). All CEDEs were far below the International Commission on Radiological Protection guideline of 100 mrem y^‐1 (1000 μSv y^‐1), and the highest muscle plus bone net CEDE corresponded to a RECF of 2E‐06, which is far below the Environmental Protection Agency upper level guideline of 1E‐04.     

Leaching of seven pesticides currently used in cotton crop in Mato Grosso State—Brazil

This study aimed to evaluate the leaching of pesticides and the applicability of the Attenuation Factor (AF) Model to predict their leaching. The leaching of carbofuran, carbendazim, diuron, metolachlor, α and β endosulfan and chlorpyrifos was studied in an Oxisol using a field experiment lysimeter located in Dom Aquino – Mato Grosso. The samples of percolated water were collected by rain event and analyzed. Chemical and physical soil attributes were determined before pesticide application to the plots. The results showed that carbofuran was the pesticide that presented a higher leaching rate in the studied soil, so was the one representing the highest contamination potential. From the total carbofuran applied in the soil surface, around 6 % leached below 50 cm. The other pesticides showed lower mobility in the studied soil. The calculated values to AF were 7.06E-12 (carbendazim), 5.08E-03 (carbofuran), 3.12E-17 (diuron), 6.66E-345 (α-endosulfan), 1.47E-162 (β-endosulfan), 1.50E-06 (metolachlor), 3.51E-155 (chlorpyrifos). AF Model was useful to classify the pesticides' potential for contamination; however, that model underestimated pesticide leaching.     

Endosulfan in China 2—emissions and residues

Background, aim, and scope  Endosulfan is one of the organochlorine pesticides (OCPs) and also a candidate to be included in a group of new persistent organic pollutants (UNEP 2007). The first national endosulfan usage inventories in China with 1/4° longitude by 1/6° latitude resolution has been reported in an accompanying paper. In the second part of the paper, we compiled the gridded historical emissions and soil residues of endosulfan in China from the usage inventories. Based on the residue/emission data, gridded concentrations of endosulfan in Chinese soil and air have been calculated. These inventories will provide valuable data for the further study of endosulfan. Methods  Emission and residue of endosulfan were calculated from endosulfan usage by using a simplified gridded pesticide emission and residue model—SGPERM, which is an integrated modeling system combining mathematical model, database management system, and geographic information system. By using the emission and residue inventories, annual air and soil concentrations of endosulfan in each cell were determined. Results and discussion  Historical gridded emission and residue inventories of α- and β-endosulfan in agricultural soil in China with 1/4° longitude by 1/6° latitude resolution have been created. Total emissions were around 10,800 t, with α-endosulfan at 7,400 t and β-endosulfan at 3,400 t from 1994 to 2004. The highest residues were 140 t for α-endosulfan and 390 t for β-endosulfan, and the lowest residues were 0.7 t for α-endosulfan and 170 t for β-endosulfan in 2004 in Chinese agricultural soil where endosulfan was applied. Based on the emission and residue inventories, concentrations of α- and β-endosulfan in Chinese air and agricultural surface soil were also calculated for each grid cell. We have estimated annual averaged air concentrations and the annual minimum and maximum soil concentrations across China. The real concentrations will be different from season to season. Although our model does not consider the transport of the insecticide in the atmosphere, which could be very important in some areas during some special time, the estimated concentrations of endosulfan in Chinese air and soil derived from the endosulfan emission and residue inventories are in general consistent with the published monitoring data. Conclusions  To our knowledge, this work is the first inventory of this kind for endosulfan published on a national scale. Concentrations of the chemical in Chinese air and agricultural surface soil were calculated for each grid cell. Results show that the estimated concentrations of endosulfan in Chinese air and soil agree reasonably well with the monitoring data in general. Recommendations and perspectives  The gridded endosulfan emission/residue inventories and also the air and soil concentration inventories created in this study will be updated upon availability of new information, including usage and monitoring data. The establishment of these inventories for the OCP is important for both scientific communities and policy makers.     

Impact of spiked concentrations of Cd,Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress)

This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment.     

Butyltin compounds in sediment and fish from the Polish Coast of the Baltic Sea

Concentrations of mono- (MBT), di- (DBT), and tri-(TBT) butyltin compounds were measured in eggs, liver, and muscle of nine species of fish from four regions of the Baltic Sea - the Firth of Vistula, the Gulf of Gdańsk, Puck Bay, and the mouth of the Vistula River. The overall concentration ranges among all the fish sampled from the four sites were: < 7 to 79 ng/g for MBT, 6 to 1100 ng/g for DBT, 7 to 3600 ng/g for TBT, and 16 to 4800 ng/g for total BTs, on a wet wt basis. The highest concentration of total BTs was found in herring liver from the Firth of Vistula (4800 ng/g, wet wt) and in roach muscle from Puck Bay (3300 ng/g, wet wt), while the least concentration was found in burbot eggs and liver from the Vistula River (39 and 32 ng/g, wet wt, respectively). TBT was the major form of BTs present in most samples analyzed. Sediment samples collected from shipyards in the Gulf of Gdańsk contained butyltin concentrations ranging from 1.2 to 46 μg/g (dry wt) for MBT, 2.0 to 42 μg/g for DBT, and 2.6 to 40 μg/g for TBT. As with the fish, the majority of the BTs in sediment were present as TBT, which suggested recent exposure of the aquatic environment of the region to TBT.     

Malathion-induced sublethal toxicity on the intestine of cricket frog (Fejervarya limnocharis)

The effect of malathion [diethyl(dimethoxythiophosphorylthio)succinate] at sublethal concentration (0.006 ppm) on intestinal parameters of cricket frog (Fejervarya limnocharis) was studied for 24 hrs to 240 hrs of exposure and remarkable histopathological alterations were observed. The study on intestinal parameters revealed acute pathological conditions in the intestinal wall. The toxic effect became evident as the cytoplasm of the cells disintegrated and the cells became empty and vacuolated. The cell membranes were also ruptured. Degenerative changes of the absorptive surface (villi) of the intestine in the different periods of exposure were pronounced. Severe atrophic nature (necrotic mucosa) of the intestine began from 48 hrs onwards to 96 hrs of exposure.