New metallothionein assay in Scrobicularia plana: heating effect and correlation with other biomarkers

Metallothionein (MT) and other biomarker levels were measured in Scrobicularia plana clams to assess pollution of the Guadalquivir Estuary possibly affected by metals released from Aznalcóllar pyrite mine in 1998. After optimizing reagent concentrations for monobromobimane derivatization, MT levels were quantified by reversed-phase high-performance liquid chromatography coupled to fluorescence detection (RP-HPLC-FD) in heated or unheated digestive gland extracts and compared to those obtained by differential pulse polarography (DPP). MT content assayed by RP-HPLC-FD in unheated samples was higher than that obtained by DPP and correlated better with metals and anti-oxidant activities. MT assay by RP-HPLC-FD in unheated extracts would be preferable for assessing metal pollution, due to its greater sensitivity and specificity. In addition to MT induction, glyoxalase II inhibition was well correlated with metal contents. Our results suggest that metals at the estuary do not originate from Aznalcóllar spill, but from those carried along by the river and deposited at its concave bank.     

废食用油活性炭脱色工艺的研究

脱色处理是提高废食用油油品质量、利用其生产生物柴油的关键环节之一.研究餐饮废食用油活性炭吸附脱色工艺,考察典型木质活性炭和煤基活性炭对脱色效果的影响,并将活性炭结构、性能指标与其脱色能力进行关联.结果表明,以弱粘性煤和褐煤为原料制备的活性炭对废食用油脱色效果较好;活性炭的总孔容积、总比表面积、微孔比表面积、微孔容积、碘值和亚甲基蓝值等性能指标与脱色效果关联度不大,而活性炭的孔径和中孔容积是决定活性炭脱色效果的主要指标.优化后废食用油活性炭脱色工艺的主要参数是:活性炭用量7%,炭粒度100～300目,脱色温度90～120℃,吸附时间为30 min,搅拌速度为10 r/min,废食用油的脱色率在50%～65%.     

城市垃圾预处理改善焚烧特性的探讨

针对目前我国城市垃圾的高水分、低热值的特性,提出了2种改善城市垃圾焚烧特性的有效措施:生物质垃圾源分类和生物干燥.在我国建立生物质垃圾源分类体系,将生物质垃圾源头分类后,剩余垃圾的热值可以提高约50%～120%,已适合直接入炉焚烧,同时分离出来的生物质垃圾也更易于好氧堆肥或厌氧消化.另外一项技术措施是在焚烧前利用生物干燥技术,降低城市垃圾的水分含量,提高入炉垃圾的热值,这种方法主要是利用生物反应热来干燥城市生活垃圾,只需要在垃圾投入焚烧炉前增加一个预处理步骤,不必改变目前的垃圾收运体系,而且进行生物干燥后的垃圾更易于分选其中的可回收物质.     

耐热乳杆菌的分离及在食物垃圾乳酸发酵中的应用

食物垃圾在我国城市生活垃圾中占有较大比重.发酵食物垃圾生产乳酸是实现其资源化的有效方法.从厌氧发酵的食物垃圾中分离到一株耐热乳酸菌TY50,根据形态、生理生化特征和16S rDNA序列,确定该菌株属于乳杆菌属的干酪乳杆菌组群(Lactobacillus casei group),其最高生长温度为52℃.TY50发酵食物垃圾生产乳酸的最佳同液比为1:12,最适温度为45 ℃.在pH 5.5～6.0条件下,发酵食物垃圾产生36.29 g/L的乳酸,乳酸体积产牢和转化率(乳峻/垃圾干重)分别达到1.01 g/(L·h)和0.44.     

A strategy for aromatic hydrocarbon bioremediation under anaerobic conditions and the impacts of ethanol: a microcosm study

Increased use of ethanol-blended gasoline (gasohol) and its potential release into the subsurface have spurred interest in studying the biodegradation of and interactions between ethanol and gasoline components such as benzene, toluene, ethylbenzene and xylene isomers (BTEX) in groundwater plumes. The preferred substrate status and the high biological oxygen demand (BOD) posed by ethanol and its biodegradation products suggests that anaerobic electron acceptors (EAs) will be required to support in situ bioremediation of BTEX. To develop a strategy for aromatic hydrocarbon bioremediation and to understand the impacts of ethanol on BTEX biodegradation under strictly anaerobic conditions, a microcosm experiment was conducted using pristine aquifer sand and groundwater obtained from Canadian Forces Base Borden, Canada. The initial electron accepter pool included nitrate, sulfate and/or ferric iron. The microcosms typically contained 400 g of sediment, 600 approximately 800 ml of groundwater, and with differing EAs added, and were run under anaerobic conditions. Ethanol was added to some at concentrations of 500 and 5000 mg/L. Trends for biodegradation of aromatic hydrocarbons for the Borden aquifer material were first developed in the absence of ethanol, The results showed that indigenous microorganisms could degrade all aromatic hydrocarbons (BTEX and trimethylbenzene isomers-TMB) under nitrate- and ferric iron-combined conditions, but not under sulfate-reducing conditions. Toluene, ethylbenzene and m/p-xylene were biodegraded under denitrifying conditions. However, the persistence of benzene indicated that enhancing denitrification alone was insufficient. Both benzene and o-xylene biodegraded significantly under iron-reducing conditions, but only after denitrification had removed other aromatics. For the trimethylbenzene isomers, 1,3,5-TMB biodegradation was found under denitrifying and then iron-reducing conditions. Biodegradation of 1,2,3-TMB or 1,2,4-TMB was slower under iron-reducing conditions. This study suggests that addition of excess ferric iron combined with limited nitrate has promise for in situ bioremediation of BTEX and TMB in the Borden aquifer and possibly for other sites contaminated by hydrocarbons. This study is the first to report 1,2,3-TMB biodegradation under strictly anaerobic condition. With the addition of 500 mg/L ethanol but without EA addition, ethanol and its main intermediate, acetate, were quickly biodegraded within 41 d with methane as a major product. Ethanol initially present at 5000 mg/L without EA addition declined slowly with the persistence of unidentified volatile fatty acids, likely propionate and butyrate, but less methane. In contrast, all ethanol disappeared with repeated additions of either nitrate or ferric iron, but acetate and unidentified intermediates persisted under iron-enhanced conditions. With the addition of 500 mg/L ethanol and nitrate, only minor toluene biodegradation was observed under denitrifying conditions and only after ethanol and acetate were utilized. The higher ethanol concentration (5000 mg/L) essentially shut down BTEX biodegradation likely due to high EA demand provided by ethanol and its intermediates. The negative findings for anaerobic BTEX biodegradation in the presence of ethanol and/or its biodegradation products are in contrast to recent research reported by Da Silva et al. [Da Silva, M.L.B., Ruiz-Aguilar, G.M.L., Alvarez, P.J.J., 2005. Enhanced anaerobic biodegradation of BTEX-ethanol mixtures in aquifer columns amended with sulfate, chelated ferric iron or nitrate. Biodegradation. 16, 105-114]. Our results suggest that the apparent conservation of high residual labile carbon as biodegradation products such as acetate makes natural attenuation of aromatics less effective, and makes subsequent addition of EAs to promote in situ BTEX biodegradation problematic.     

Determination of 10 particle-associated multiclass polar and semi-polar pesticides from small streams using accelerated solvent extraction

A new analytical method using accelerated solvent extraction was developed for the determination of 10 particle-associated polar and semipolar pesticides. In addition, six deuterated analogues of the target compounds were evaluated as internal standards. The method yielded acceptable accuracy (73–103% recovery) and precision (<25% relative standard deviation) for eight compounds. Using size exclusion chromatography (SEC) as cleanup step resulted in higher recoveries compared to solid phase extraction (SPE) cleanup.

Deuterated standards with 10 or more deuterium atoms performed well as internal standards concerning similar recovery and correlation with the target analytes.

The method was employed to extract particle-associated pesticides from 16 streams located in an area with intense agriculture in France. Acetochlor, pirimicarb, tebuconazole, fenpropidin, -endosulfan and chlorfenvinphos were detected at concentrations up to 1 mg kg⁻¹ dry weight. A comparison with aquatic toxicity data indicated potential risk to the benthic fauna exposed to these concentrations of pirimicarb, -endosulfan and chlorfenvinphos.

We suggest that the method presented here be used for the extraction and quantitation of particle-associated polar pesticides.     

离子色谱法测废印刷电路板真空热解气相污染物中HBr、NO2和SO2

在淋洗液中加入H2O2和三乙醇胺配制成吸收液,通过离子色谱法同时测定废印刷电路板真空热解气相产物中HBr、NO_2和SO_2的含量,方法简单、快速、准确。当用50 m L吸收液、采样体积为30 L时,3种污染物的检出限分别为0.000 005 7、0.000 003 4、0.000 002 9 mg/L。该方法加标回收率为95.7%~104.8%,完全能满足废印刷电路板真空热解气相污染物中HBr、NO_2和SO_2的同时测定要求。利用该方法和行标方法同时测定环境空气中的HBr、NO_2和SO_2,再利用Excel分析工具对测定数据进行F检验和t检验,检验结果表明2种测定方法无显著差异。     

果皮、菜叶混合垃圾的蚯蚓堆制处理

在果皮、菜叶混合垃圾中,加入不同比例木屑调节C／N比值和含水量后,接种赤子爱胜蚓（Eisenia foetida）进行室内堆制处理,研究适宜含水量、接种密度和温度条件下蚯蚓的生长和繁殖特性以及堆制产物的化学性状。结果表明：蚯蚓堆制处理明显加速有机质矿化,促进有机物料降解,提高堆制产物全N量,降低堆制产物有机C含量和C／N比值。加入木屑虽然在一定程度上抑制了蚯蚓的生长和繁殖,但是,0～30d时25％和40％木屑堆制处理中赤子爱胜蚓生长良好,繁殖较旺盛。相关分析表明,接种蚯蚓并加入25％～40％木屑对促进果皮、菜叶垃圾降解以及提高和改善其化学性状是有效可行的,有利于废弃物的减量化、无害化和资源化。     

pH值与乙酸对易腐有机垃圾水解过程的抑制

通过外部添加水解酶比较和区分pH值和乙酸对水解的影响,结果表明:以固相挥发性固体和元素碳的减少以及液相有机碳的增加表征水解率,在pH=7时最大,144h的水解率可达66.9%;与pH=7相比,pH=8-9时,水解率降低8%-24%;pH=5-6,水解率降低40%-60%.20g·l-1乙酸的加入抑制了水解,在不同pH值条件下与不添加乙酸的水解相比,抑制程度为2%-35%,pH=7时乙酸的抑制最显著,可达35%.颗粒态物料的水解过程动力学符合Chen-Hashimoto公式.     

废弃物燃烧生成的可吸入颗粒物中多环芳烃的排放特性

将木粉、谷壳、甘蔗渣、垃圾衍生燃料(RDF)四种废弃物在两种过量空气系数下进行燃烧,采集其烟气中的可吸入颗粒物(PM10)样品并分析,获得了颗粒物中多环芳烃的质量分数和排放特性,并对不同环数的芳烃进行了比较,最后分析了不同样品中的多环芳烃的毒性参数.