直颈双口卧式便携水样采集器

设计了一种具有结构简便、操作方便、易于清洗和采样杆可续接的直颈双口卧式便携水样采集器。该采样器不仅适合采集水层很浅水体的水样。也能用于采集江河、湖库水体的水样。     

国内含油水样采集方法分析

综述了目前国内报道的几种测定油含量的水样采集设备及方法,评述了其优缺点,提出了设计思想及展望。     

应用水跃区流体动力学特性提高含油污水采样的代表性

含油污水采样代表性问题是目前一个尚未解决的技术问题,利用水跃区的流体动力学特性,可使含油污水得到充分地混合,提高水样的代表性。     

利用Triolein半渗透膜采样技术测定洋河水中的优先污染物

应用Ｔｒｉｏｌｅｉｎ半渗透膜采样器采集了河北洋河宣化至官厅水库河段水样,根据测定采样器中多氯联苯污染物（ＰＣＢｓ）及其它优先污染物浓度,可以估算这些污染物在河段水体中的平均浓度。将结果与同时同地采集的水样,经萃取浓缩后分析得到的结果比较,发现对于不同类型污染物,二者符合程度不同。本研究证明半渗透膜被动采样技术可用于水中多氯联苯等难降解污染物的定量监测,有可能在我国的优先污染物监测工作中发挥作用     

简易吸水式深水采样器的制作与应用

常用的直通式深水采样器不但价格较高,且使用不方便。本文介绍一种简单、实用的吸水式深水采样器,具有造价低廉、操作简单、方便实用的优点,尤其适用于河流湖库的深层水样采集,采水深度可达１００ｍ左右。     

环境水样的汞、铬、砷及重金属保存

本文论述了在采集水样时,可能引起水样变化,不能反映水体真实情况,失去其代表性的各种影响因素。综述了贮存容器材质的影响,水样的过滤方式,及测定Hg、Cr、As和重金属水样的保存条件和允许保存的时间。     

地面水水样中氨氮稳定性试验

按ＧＢ７４８０－８７规定氨氮水样滴加硫酸酸化至ｐＨ≤２,最长保存时间为２４ｈ。常规监测需要采集大量水样,分析项目较多,在２４ｈ内采样分析,给分析人员带来一定困难。今对三氮水样进行了保存时间稳定性试验。结果发现,除了亚硝酸盐氮、硝酸盐氮不宜保存外,氨氮...     

水样保存条件对COD测定的影响

影响ＣＯＤ测定的因素较多 ,今主要对两种水样的保存期进行了验证试验。《水和废水监测分析方法 (第 3版 )》规定 ,测定ＣＯＤ的水样加了固定剂和在冷藏条件下可保存 7ｄ ,但工作中发现即使水样在这样的保存条件下其ＣＯＤ的含量仍在不断下降。为此分别采集了运河王江泾地表水     

含油废水平行样的制备

扼要阐述了应用“超声空化”技术制备含油废水平行样的原理和方法，并通过各因素正交试验，优选出“超声空化”技术制备含油废水平行样品最优条件。     

试论地表水采样技术

1.采样的前期准备工作在现今条件下,全面采用自动采样器采集水样是不现实的.大多数情况下仍是采用人工采样的方式进行.现将地表水采样所必备的器具、试剂列于表1.表中所用器具及试剂的规格、长度、数量等,可根据采样点位的多少及采样位置的实际情况而自行确定.对需采集深层水样的,应增     

Performance optimisation of a passive sampler for monitoring hydrophobic organic pollutants in water

The performance of an integrative passive sampler that consists of a C18 Empore disk sorbent receiving phase fitted with low density polyethylene membrane was optimised for the measurement of time-weighted average concentrations of hydrophobic micropollutants in water. A substantial improvement of sampling characteristics including the rate of sampling and the sampling precision was achieved by decreasing the internal sampler resistance to mass transfer of hydrophobic organic chemicals. This was achieved by adding a small volume of n-octanol, a solvent with high permeability (solubility [times] diffusivity) for target analytes, to the interstial space between the receiving sorbent phase and the polyethylene diffusion-limiting membrane.     

Development of an integrative passive sampler for the monitoring of organic water pollutants

The development of convenient and competitive devices and methods for monitoring of organic pollutants in the aquatic environment is of increasing interest. An integrative passive sampling system has been developed which consists of a solid poly(dimethylsiloxane) (PDMS) material (tube or rod), acting as hydrophobic organic receiving phase, enclosed in a water-filled or an air-filled low-density polyethylene (LDPE) membrane tubing. These samplers enable the direct analysis of the pollutants accumulated during exposure in the receiving phase by thermodesorption-GC/MS, avoiding expensive sample preparation and cleanups. The capabilities of these sampling devices were studied for the sampling of 20 persistent organic pollutants (chlorobenzenes, hexachlorocyclohexanes, p,p'-DDE, PAHs, and PCBs) in laboratory exposure experiments. For the three sampler designs investigated the uptake of all target analytes was integrative over exposure periods up to 9 days (except PCB 101). The determined sampling rates range from 4 to 1340 microl h(-1) for the water-filled samplers and from 20 to 6360 microl h(-1) for the air-filled ones, respectively. The sampling rate of the analytes is dependent on their molecular weight, partition between water and sampler media (PDMS, polyethylene, water, air) and also of the sampler design. The passive samplers enable the estimation of time-weighted average (TWA) concentration of water pollutants in the lower ng l(-1) to pg l(-1) range.     

Efficiency of a standardized artificial substrate for biological monitoring of river water quality

Before using macroinvertebrates in water quality assessment in the Chusovaya River (Russia, the Urals, 50°55N, 60° E), preliminary results of three sampling methods were compared: handnet, circular shovel and a standardized artificial substrate sampler. The artificial substrate consisted of glass marbles ( 20 mm). To compare the efficiency of these sampling methods the total numbers of taxa found at each location per sampling data were considered to be 100%. The highest efficiency was reached with the artificial substrate sampler. 75–100% of the taxa at the different locations were collected with this sampler. Only 5–19% and 10–20% of the taxa at each location per sampling date were collected with the circular shovel in the sand and gravel substrate respectively, being the lowest efficiency. Intermediate results were obtained with the hand net. 23–38% of the taxa were collected with this net. Based on these results and requirements placed upon sampling methods in general, the standardized artificial substrate sampler has been considered to be an optimal sampling device for macroinvertebrates in biological monitoring.     

Dry deposition study by using dry deposition plate and water surface sampler in Shalu, central Taiwan

This study presents the chemical composition of dry deposition by using dry deposition plate and water surfaces sampler during daytime and nighttime sampling periods at a near highway traffic sampling site. In addition, the characterization for mass and water soluble species of total suspended particulate (TSP), PM2.5 and PM10 were also studied at this sampling site during August 22 to October 31 of 2006 around central Taiwan. The samples collected were analyzed by using Ion Chromatography (DIONEX 100) for the ionic species analysis. Results of the particulate dry deposition fluxes are higher in the water surfaces sampler than that of the dry deposition plate. In other words, the results also indicated that water surface can absorb more ambient dry deposition inorganic pollutants than that of dry deposition plate in this study. The results obtained in this study indicated that the ionic species of Cl(-), NO3(-) and SO4(2-) occupied about average 60-70% downward flux out of total ionic species for either dry deposition plate or water surfaces sampler during August to October of 2006 at this near highway traffic sampling site.     

Performance optimization of a membrane assisted passive sampler for monitoring of ionizable organic compounds in water

A thin-walled silicone rubber hollow fibre membrane has been developed as a passive sampler. The inside of the tube is filled with an aqueous solution at an appropriate pH. The tube is sealed at both ends and then immersed in a water sample. In order for the ionizable permeating compounds to be trapped in the aqueous receiving phase, the pH is adjusted such that the compounds are ionized and trapped. The major advantages are its simplicity, low cost and high selectivity, since only ionizable organic compounds are trapped. Additionally, the sampler uses no organic solvent. By adjusting the pH of the acceptor phase, it is possible to control the extraction process and whether the sampler is used in the kinetic or equilibrium regime. Since it is very selective, no further clean-up of the extract is required. The membrane assisted passive sampler has been tested for extraction of chlorophenols under laboratory conditions. The extraction process was found to be linear over a 72 h sampling period. Selectivity of the passive sampler in river water was demonstrated and the extraction process was independent of sample concentration, even at lower concentration levels of analytes. However, the sample matrix in some river water samples led to incomplete trapping, thereby reducing the amount trapped in the acceptor phase. Detection limits (three times signal to noise ratio) were dependant on sample matrix and type of detection system and ranged from 0.05 microg L(-1) to about 1 microg L(-1) with a UV photodiode detector in water samples from one river and 1.0 microg L(-1) to 20 microg L(-1) in another but with an ordinary UV detector. The enrichment factors in river water were 28 for 2-chlorophenol and 44 for 2,4-dichlorophenol over a 72 h sampling period. 4-chlorophenol was poorly extracted and its enrichment factor was 3.     

Development of a diffusive sampling method for determination of methyl isocyanate in air

A diffusive sampling method for determination of methyl isocyanate in air has been developed. A glass fibre filter impregnated with 1-(2-methoxyphenyl)piperazine in a commercially available diffusive sampling device was used to collect methyl isocyanate and the derivative formed was analysed with LC-MS/MS. The sampling rate was determined to be 15.6 ml min(-1), with a relative standard deviation of 7.3%. The sampler was validated for sampling periods from 15 min to 8 h, for relative humidities from 20% to 80% and for concentrations from I to 46 microg m(-3). A field validation was also made and the diffusive sampling results showed no difference compared to a pumped reference method. The impregnated filters have to be stored apart from the diffusive sampler housing and loaded into the sampler prior to each sampling.     

Chemcatcher and DGT passive sampling devices for regulatory monitoring of trace metals in surface water

This work aimed to evaluate whether the performance of passive sampling devices in measuring time-weighted average (TWA) concentrations supports their application in regulatory monitoring of trace metals in surface waters, such as for the European Union's Water Framework Directive (WFD). The ability of the Chemcatcher and the diffusive gradient in thin film (DGT) device sampler to provide comparable TWA concentrations of Cd, Cu, Ni, Pb and Zn was tested through consecutive and overlapping deployments (7-28 days) in the River Meuse (The Netherlands). In order to evaluate the consistency of these TWA labile metal concentrations, these were assessed against total and filtered concentrations measured at relatively high frequencies by two teams using standard monitoring procedures, and metal species predicted by equilibrium speciation modeling using Visual MINTEQ. For Cd and Zn, the concentrations obtained with filtered water samples and the passive sampling devices were generally similar. The samplers consistently underestimated filtered concentrations of Cu and Ni, in agreement with their respective predicted speciation. For Pb, a small labile fraction was mainly responsible for low sampler accumulation and hence high measurement uncertainty. While only the high frequency of spot sampling procedures enabled the observation of higher Cd concentrations during the first 14 days, consecutive DGT deployments were able to detect it and provide a reasonable estimate of ambient concentrations. The range of concentrations measured by spot and passive sampling, for exposures up to 28 days, demonstrated that both modes of monitoring were equally reliable. Passive sampling provides information that cannot be obtained by a realistic spot sampling frequency and this may impact on the ability to detect trends and assess monitoring data against environmental quality standards when concentrations fluctuate.     

Verification of a depth-integrated sample arm as a means to reduce solids stratification bias in urban stormwater sampling

A new water sample collection system was developed to improve representation of solids entrained in urban stormwater by integrating water-quality samples from the entire water column, rather than a single, fixed point. The depth-integrated sample arm (DISA) was better able to characterize suspended-sediment concentration and particle size distribution compared to fixed-point methods when tested in a controlled laboratory environment. Median suspended-sediment concentrations overestimated the actual concentration by 49 and 7% when sampling the water column at 3- and 4-points spaced vertically throughout the water column, respectively. Comparatively, sampling only at the bottom of the pipe, the fixed-point overestimated the actual concentration by 96%. The fixed-point sampler also showed a coarser particle size distribution compared to the DISA which was better able to reproduce the average distribution of particles in the water column over a range of hydraulic conditions. These results emphasize the need for a water sample collection system that integrates the entire water column, rather than a single, fixed point to properly characterize the concentration and distribution of particles entrained in stormwater pipe flow.     

A new sampler for stratified lagoon chemical and microbiological assessments

A sampler was needed for a spatial and temporal study of microbial and chemical stratification in a large swine manure lagoon that was known to contain zoonotic bacteria. Conventional samplers were limited to collections of surface water samples near the bank or required a manned boat. A new sampler was developed to allow simultaneous collection of multiple samples at different depths, up to 2.3 m, without a manned boat. The sampler was tethered for stability, used remote control (RC) for sample collection, and accommodated rapid replacement of sterile tubing modules and sample containers. The sampler comprised a PVC pontoon with acrylic deck and watertight enclosures, for a 12 VDC gearmotor, to operate the collection module, and vacuum system, to draw samples into reusable autoclavable tubing and 250-mL bottles. Although designed primarily for water samples, the sampler was easily modified to collect sludge. The sampler held a stable position during deployment, created minimal disturbance in the water column, and was readily cleaned and sanitized for transport. The sampler was field tested initially in a shallow fresh water lake and subsequently in a swine manure treatment lagoon. Analyses of water samples from the lagoon tests showed that chemical and bacterial levels, pH, and EC did not differ between 0.04, 0.47, and 1.0 m depths, but some chemical and bacterial levels differed between winter and spring collections. These results demonstrated the utility of the sampler and suggested that future manure lagoon studies employ fewer or different depths and more sampling dates.     

A novel passive water sampler for in situ sampling of antibiotics

Passive water sampling has several advantages over active methods; it provides time-integrated data, can save on time and cost compared to active methods, and yield high spatial resolution data through co-deployment of simple, cheap units. However, one problem with many sampler designs in current use is that their uptake rates for trace substances of interest are flow-rate dependent, thereby requiring calibration data and other information to enable water concentrations to be derived from the mass per sampler. However, the 'family' of samplers employing the principle of diffusive gradients in thin films (DGT) provides an in situ means of quantitatively measuring labile species in aquatic systems without field calibration. So far, this technique has only been tested and applied in inorganic substances: metals, radionuclides, nutrients, etc. Design and applications of DGT to trace organic contaminants ('o-DGT') would be of widespread interest. This study describes the laboratory testing and performance characteristics of o-DGT, with the antibiotic sulfamethoxazole (SMX) as a model compound and XAD18 as the novel binding agent. o-DGT uptake of SMX increased with time and decreased with diffusion layer thickness, confirming the principle for SMX. XAD18 showed sufficiently high capacity for SMX for routine field applications. o-DGT measurement of SMX was independent of pH (6-9) and ionic strength (0.001-0.1 M) and not affected by flow rate once above static conditions. The diffusion coefficient of SMX in the sampler was measured using an independent diffusion cell and information is presented to allow temperature correction and derivation of aqueous concentrations from deployed samplers. The potential use of o-DGT for in situ measurement of pharmaceutical antibiotics is confirmed by this study and applications are briefly discussed.