IMS Method Performance Analyses for Giardia in Water Under Differing Conditions

Immunomagnetic separation (IMS) has been specified as a standard method for the measurement of Giardia under USEPA Method 1623. In this study, IMS was evaluated on the basis of recovery efficiencies for Giardia cysts under various IMS operation conditions. Significant change in recovery was observed by altering the debris ratio of water samples. Notably, cyst recovery efficiencies utilizing IMS dropped with increased turbidity, and results for varying dosages of magnetic beads and cysts indicate that 1 / 100 immunomagnetic beads is sufficient to conjugate large numbers of cysts. Changing vessel volume and replacing the sample buffer had no significant effect on cyst recovery efficiencies.     

SBR与SBBR法处理制药废水对比试验

制药废水属于高浓度含微生物难降解,对微生物有抑制作用的有机废水,水质水量波动大,本文对制药厂厌氧处理出水,分别采用SBR和SBBR法进行对比试验,研究其COD去除效果。当曝气量控制在0.02m3/h,沉淀时间在2h时,在2~10h反应时间段内,对比了SBR和SBBR法对CODCr的去除率。试验结果表明:总体上,SBBR法CODCr去除效果优于SBR,且更稳定,CODCr去除率能达到90%以上,而SBR在反应时间6h时达到CODCr最大去除率:82.03%后,出水中CODCr不降反升。     

用磷酸铵镁沉淀法去除沈阳老虎冲垃圾渗滤液中的氨氮

叙述了磷酸铵镁沉淀法去除垃圾渗滤液中氨氮的基本原理,分析了MAP法对氨氮的去除效果,对比了不同的镁盐及不同的反应时间对氨氮的去除效率。结果表明,MAP法对氨氮的去除效率高,产物中重金属的含量低。同时,氧化镁比氯化镁具有更好的氨氮去除综合优势。     

污泥中重金属的去除及回收试验

论述了利用离子交换技术循环使用柠檬酸去除污泥中重金属,并置换回收重金属的适宜工艺条件.经柠檬酸处理后,污泥中90%以上的重金属被去除;柠檬酸处理液中的重金属用离子交换法回收,考察了树脂种类、流速、操作方式等因素对离子交换、再生效果的影响;在适宜工艺条件下,重金属的交换率均为100%,而洗脱率均接近90%;柠檬酸及离子交换树脂循环使用,重金属也得到回收,降低了处理成本.     

探究土壤中萘提取液的浓缩方法比较

随着科学技术的发展,工业产品越来越丰富。工业工艺过程、缺氧燃烧、垃圾焚烧和填埋等生产活动,产生了大量的多环芳烃物质。这些物质通过复杂的物理迁移、化学及生物转化反应,进入土壤,严重污染环境,给人类及其生物的安全带来严重危害。如何快速、准确检测土壤中多环芳烃的含量,成为治理污染等相应策略实施的首要条件。当前测定土壤中多环芳烃的前处理方法有加压流体萃取、索式萃取、超声波萃取、微波萃取等。在这些成熟萃取手段中,浓缩又是一个关键步骤。目前浓缩的手段有KD浓缩、氮吹浓缩、旋转蒸发浓缩、旋转与氮吹合用浓缩。本文对四种浓缩手段对多环芳烃中的萘提取液进行浓缩分析比较,并获得了一定结论,望给行业内提供有效的参考意见。     

Assessment of organochlorine pesticide residues in Atlantic Rain Forest fragments, Rio de Janeiro, Brazil

A superficial water quality survey in a watershed of the Paraíba do Sul River, the main water supply for the most populated cities of southeastern Brazil, was held in order to assess the impact of the expansion of agricultural activity in the near border of the Atlantic Rain Forest. The aim of this study was to investigate the presence of priority organochlorine pollutants in soils and superficial waters of Atlantic rainforest fragments in Teresópolis, Rio de Janeiro State. Soil sample preparations were compared by using ultrasound, microwave assisted extraction and Soxhlet extraction. Recoveries of matrix spiked samples ranged from 70 to 130%. Analysis of a certified soil material showed recoveries ranging from 71 to 234%. Although low concentrations of organochlorine residues were found in water and soil samples, this area is of environmental importance and concern, thus demanding a monitoring program of its compartments.     

An Approach for Evaluating the Repeatability of Rapid Wetland Assessment Methods: The Effects of Training and Experience

We sampled 92 wetlands from four different basins in the United States to quantify observer repeatability in rapid wetland condition assessment using the Delaware Rapid Assessment Protocol (DERAP). In the Inland Bays basin of Delaware, 58 wetland sites were sampled by multiple observers with varying levels of experience (novice to expert) following a thorough training workshop. In the Nanticoke (Delaware/Maryland), Cuyahoga (Ohio), and John Day (Oregon) basins, 34 wetlands were sampled by two expert teams of observers with minimal protocol training. The variance in observer to observer scoring at each site was used to calculate pooled standard deviations (SD_pool), coefficients of variation, and signal-to-noise ratios for each survey. The results showed that the experience level of the observer had little impact on the repeatability of the final rapid assessment score. Training, however, had a large impact on observer to observer repeatability. The SD_pool in the Inland Bay survey with training (2.2 points out of a 0–30 score) was about half that observed in the other three basins where observers had minimal training (SD_pool = 4.2 points). Using the results from the survey with training, we would expect that two sites assessed by different, trained observers who obtain DERAP scores differing by more than 4 points are highly likely to differ in ecological condition, and that sites with scores that differ by 2 or fewer points are within variability that can be attributed to observer differences.     

不同经济发展阶段区域经济发展差异比较

在介绍区域经济发展阶段各种理论及划分方法的基础上,通过计算1985-2004年间,广西崇左市、安徽滁州市、江苏南通市经济发展的变化轨迹,确定不同区域经济发展阶段.利用偏离-份额分析法对区域经济发展水平进行研究,表明崇左市经济结构较差,结构对于经济增长的贡献小且竞争能力较弱;滁州市经济中增长快的产业部门比重较大,总体经济结构较好,结构对于经济增长具有一定贡献,竞争能力较强;南通市经济中朝阳的、增长快的产业部门比重大,总体经济结构好,结构对于经济增长的贡献大,且各产业部门总的增长势头大,具有很强的竞争能力.建议:①崇左市参与中国-东盟自由贸易区、中越"两廊一圈"经济带以及泛珠三角经济区域,吸收泛珠三角经济区的产业转移,加快发展国际贸易.②滁州市应融入南京都市圈,吸引和承接东部地区的产业转移,注意生态城市建设,发展循环经济,实现经济和生态环境的综合协调发展.③南通市应把资源节约型的增长模式和消费方式作为经济增长方式转变的核心,提升产业的综合竞争力,最终实现经济社会协调发展.     

Extraction and clean-up methods for organochlorine pesticides determination in milk

Organochlorine pesticides (OCPs) can cause environmental damage and human health risks since they are lipophilic compounds with high resistance to degradation and long half-lives in humans. As most persistent OCPs have been banned years ago, it is expected to find these compounds at trace levels in environment. Therefore, increasingly sensitive and reliable analytical techniques are required to ensure effective monitoring of these compounds. The aim of this review is to discuss extraction and clean-up methods used to monitor OCP residues in milk, reported in the last 20 years. To carry out this review, an exhaustive bibliographic review was conducted. Despite the disadvantages of conventional extraction and clean-up methods, such as liquid–liquid, solid-phase or Soxhlet extractions, these procedures are still used due to their reliability. New extraction methods, like solid-phase microextraction, matrix solid-phase dispersion or QuEChERS, have not been thoroughly evaluated for OCP determination in milk. Almost all the methodologies analyzed in this review presented good performance characteristics according to the performance acceptability criteria set in SANCO’s procedure. Comparison between limits of quantification (LOQ) and detection (LOD), for the reported methodologies, is not always possible due to the heterogeneity of the units. Thus, researchers should take into account an homogenization of LOD and LOQ units, according to the international regulations and MRLs established. Finally, more research is necessary to obtain the ideal methodology for OCPs determination in milk, which comprises the environmentally friendly characteristics of the new techniques and the reliability of the traditional methodologies.     

Method Development for Determination of Fluroxypyr in Soil

Abstract

Four methods were developed for the analysis of fluroxypyr in soil samples from oil palm plantations. The first method involved the extraction of the herbicide with 0.05 M NaOH in methanol followed by purification using acid base partition. The concentrated material was subjected to derivatization and then cleaning process using a florisil column and finally analyzed by gas chromatography (GC) equipped with electron capture detector (ECD). By this method, the recovery of fluroxypyr from the spiked soil ranged from 70 to 104% with the minimum detection limit at 5 µg/kg. The second method involved solid liquid extraction of fluroxypyr using a horizontal shaker followed by quantification using high performance liquid chromatography (HPLC) equipped with UV detector. The recovery of fluroxypyr using this method, ranged from 80 to 120% when the soil was spiked with fluroxypyr at 0.1–0.2 µg/g soil. In the third method, the recovery of fluroxypyr was determined by solid liquid extraction using an ultrasonic bath. The recovery of fluroxypyr at spiking levels of 4–50 µg/L ranged from 88 to 98% with relative standard deviations of 3.0–5.8% with a minimum detection limit of 4 µg/kg. In the fourth method, fluroxypyr was extracted using the solid liquid extraction method followed by the cleaning up step with OASIS® HLB (polyvinyl dibenzene). The recovery of fluroxypyr was between 91 and 95% with relative standard deviations of 4.2–6.2%, respectively. The limit of detection in method 4 was further improved to 1 µg/kg. When the weight of soil used was increased 4 fold, the recovery of fluroxypyr at spiking level of 1–50 µg/kg ranged from 82–107% with relative standard deviations of 0.5–4.7%.