国产有机微孔滤膜的结构与性能

作为水样分析用的滤器很多,有人根据刚度对过滤介质做了分类。在所有这些过滤器中,仅有有机微孔滤膜的孔径尺寸符合环境水样分析0.45微米(可溶性成份)孔径的要求。为使国内与国外的监测数据具有可比性,因而要求环境水样分析中必须选用孔径为0.45微米的过滤器。     

地表水泥沙与总磷测定值的相关性分析

为研究总磷与泥沙之间的质量浓度关系,采集了三峡库区7个断面的地表水样品,通过筛分、滤膜过滤等方式,分离了水样中不同粒径的泥沙,得到含不同泥沙质量浓度的水样,并同步分析了水样中泥沙和总磷的质量浓度.结果表明,在丰水期,总磷主要来源于泥沙中吸附的有机磷和无机磷,而溶解态磷较少.泥沙与总磷质量浓度可以用线性关系和对数关系模拟,泥沙是影响地表水中总磷测定结果的主要原因之一.     

氨荒酸膦酸树脂滤器的制备及其在AAS分析中的应用研究

介绍了氨荒酸膦酸树脂过滤器的制备方法,以及应用该过滤器分离与富集地面水(海水)中Cu、Pb、Zn、Cd等元素的适用条件。实际样品中的Cu、Pb、Zn、Cd等重金属离子经过过滤器过滤,被吸附在树脂滤层中,用少量酸洗脱,以AAS测试,结果稳定、准确度高。此过滤器在痕量分析中具有很高的应用价值。     

固相萃取-气相色谱法测定饮用水中甲基汞

根据巯基棉在一定酸性条件下能定量吸附甲基汞的原理,利用多通道并联的固相萃取装置,采用气相色谱(ECD)方法测定饮用水中痕量甲基汞,考察了水样pH值对回收率的影响.方法在0.050 mg/L～1.00 mg/L范围内线性良好,当采样体积为1.0 L时,检出限为0.03 ng/L,标准样品与实际水样平行测定的相对标准偏差均...     

焦炉烟气中复杂有机污染物筛选研究(Ⅰ):采样技术与方法

借鉴国内外典型烟气采样装置,设计出多级串联采样装置.它将多种过滤、吸附材料联合使用,具有一次采集有机污染物种类全,数量多,结构简单,操作方便,适用范围广等特点,实际采集鞍钢焦炉烟气样品,效果很好.     

大水量采样器,采样技术在环境监测中的应用

在环境监测工作中,采样是重要步骤,一些先进国家的环境保护机构对发展水中痕量污染物的富集采样技术极为重视,自动采样器(装置)得到广泛应用.美国国家环保局(EPA)下属的辛辛那提环境监测与支持实验室编著的《水与废水采样及样品保存手册》一书,专门介绍了一些自动采样器,认为自动采样器的使用为进行环境污染监测和筛选环境水样中的优先监测物和致突变物质,提供了方便,使过去因工作量大而无法广泛开展的工作成为可能.采样器以及采样技术的发展水平反映了一个国家环境监测水平.     

氟氯烃检测中的富集采样研究

本文用自制的吸附采样管和解吸装置完成了大气中痕量氟氯烃的采样测定，其吸附效率达８５％以上，解吸效率达８７％，富集倍数达１１４４倍。研究了温度对吸附和解吸效率的影响。     

在线富集固相萃取-超高效液相色谱串联质谱法测定地表水中对硝基苯酚

建立了在线富集固相萃取-超高效液相色谱串联质谱法测定水中对硝基苯酚的方法。经过滤的水样用在线固相萃取系统富集后,以氨水-甲醇系统作为流动相进行梯度洗脱,通过超高效液相色谱串联质谱仪进行检测。方法的检出限为3. 52 ng/L,回收率为91. 6%～108%,相对标准偏差为5. 5%～9. 5%。该方法可大大简化复杂的前处理过程,提高灵敏度及准确性,可用于大批量地表水中对硝基苯酚的测定。     

水系环境背景值调查中Zn的污染来源

由于水系环境背景值调查研究工作的需要,我们用原子吸收光谱法测定了嘉陵江水系中铜铅锌镉铁钴镍铬锰和钒等十个元素,结果发现,绝大多数元素都能满足环境背景值分析测试质量控制的要求,只有锌出现了溶解态锌(经0.45μ微孔滤膜过滤后过滤水中的锌量)超过总量锌(未经过滤的原水中的锌量)的倒置现象。为了寻找产生倒置的原因,本文从使用的分析方法、存器、滤膜、导水管和环境等各个方面,研究了锌分析结果不正常的原因,通过实验证明,过滤时用的导水管材料不当,和过滤时的环境是污染的主要原因。本文还通过锌等元素的测定,探讨了过滤水样用的微孔滤膜处理方法,方法简单方便,可以避免滤膜和器皿的污染。     

水中可吸附有机氯(AOCl)的测定——离子色谱法

采用自制的燃烧装置,使吸附在活性炭上的有机氯定量地转化为无机氯,经硼砂双氧水溶液吸收,用离子色谱法分离测定。当富集水样的体积为５０～２００ｍｌ时,可测定可吸附有机氯（ＡＯＣｌ）的范围为２８～１０００μｇ／Ｌ。当样品中ＡＯＣｌ含量在１６～６４μｇ时,平均加标回收率大于９０％,相对标准偏差小于１０％。用该方法还可同时测定水中可吸附有机硫。     

Shipboard techniques based on flow injection analysis for measuring dissolved Fe, Mn and Al in seawater

An overview is presented of sampling techniques and flow injection analysis (FIA) methods for low concentrations of Fe, Mn and Al in filtered seawater. On the basis of sampling procedures, filtration techniques, accuracy, blanks, detection limits, intercalibration results and oceanographic consistency, the feasibility of these FIA methods was evaluated. It was found that these metals could be measured on board with a minimum risk of contamination and with good accuracy even at low subnanomolar levels (<0.5 nM). Results for reference seawater were in the case of Fe-FIA and Mn-FIA in excellent agreement with the certified values. Data from samples analyzed by Fe-FIA and by cathodic stripping voltametry (CSV) compared well, as did Mn-FIA and GFAAS. All three methods gave results that were mostly in good agreement with data from the same ocean regions published by other research groups. Two different types of surface water sampling were also tested and compared, namely conventional hand filling of a sample bottle from a rubber dinghy away from the ship, and underway pumping of seawater using a 'tow fish'. The latter method gave the best results. Also, conventional membrane filtration and cartridge filtration for large volume filtration were compared using Fe and Al data from water column samples. Good agreement was found for both filter types, although for defining dissolved metal species the latter filter type was preferred.     

Application of Non-Conventional Filtration Technologies in Pollution Control

Deep bed filtration is becoming increasing important in wastewater treatment particularly in tertiary treatment as stringent water quality standards are emphasized. A detailed pilot-scale filtration study conducted with secondary effluent in a sewage treatment plant indicated that tertiary filtration with prior alum flocculation is capable of producing high quality effluent, particularly an effluent with phosphorus content of less than 0.3 mg/L (Vigneswaran and Ngo, 1994). Main problem of dual media filter has been rapid headloss development thus frequent backwash requirement. To overcome this problem two independent experimental studies were conducted: one with mobile bed filtration (MBF) and the other with combined downflow floating medium flocculator/prefilter (DFF) and coarse sand filter (CSF) system. A semi-pilot scale mobile bed filtration study conducted using oxidation pond effluent indicated that MBF with contact-flocculation arrangement was good in removing COD, T-P and turbidity with practically no headloss development. Sand of 0.6-0.84 nm dia and 50 cm depth was sufficient to reduce the COD and P from 55 mg/L and 4.5 mg/L to 15 mg/L and 0.5 mg/L respectively at a filtration rate of 7.5 m3/m2.h. Another experimental study with combined DFF-CSF system indicated that the DFF with in-line flocculation addition is a good pretreatment unit to reduce the phosphate upto 80-90%. The fact that DFF resulted in uniform filterable-flocs, it can also successfully be used as a static flocculator/prefilter unit. The introduction of DFF on top of a coarse sand filter increased the filter run time and removal efficiency (more 90-95% of NH3-N and T-P removal respectively). Most importantly, the backwashing of this system was achieved with small quantity of water at low backwash indicated that the removal efficiency was also superior with this system apart from the major advantage of low operating cost.     

Quantification of re-evaporated mass from loaded fibre-mist eliminators

Airborne lubricant emissions are a serious health hazard for employees in the metal working industry. The basic components of lubricants are oils and additives for adapting the properties to achieve the process demands. The oils used in lubricants are either mineral, synthetic or of biological origin. The lubricants are used as water-emulsions and also as straight oils. Extreme process conditions cause considerable amounts of aerosol and vapour emissions of lubricants into the working environment. Fibre filters are used in industrial demisters for pollution control and also for sampling purposes. Re-evaporation of separated lubricants from loaded fibre filters causes increased vapour emissions. Quantification of lubricant vapour emission was the subject of this research. An apparatus and an appropriate procedure for measuring the dynamic behaviour of evaporative losses from fibre filters were developed. The test piece of a loaded fibre filter was fixed in a sampling probe according to VDI 2066. The vapour concentration of organic compounds in downstream air was measured in real-time by using a photo-ionisation detector (PID). The PID was checked by sampling the vapour on an oleophilic adsorbent resin, solvent extraction and quantitative IR analysis and also gravimetrically. The two basic processes of filtering volatile aerosols are, on the one hand, collecting droplets on the fibres and, on the other hand, the evaporation of collected liquid. These two processes had to be separated in order to measure the increase of the vapour concentration caused by the tested fibre filter. The experiments were carried out using pure dodecane and hexadecane in order to avoid difficulties due to the unknown chemical composition of lubricant vapour. The variation of the air flow and the initial liquid mass on the filter covered the relevant range for industrial fibre demisters and for sampling methods based on collecting aerosols on fibre filters. It was found that the downstream air was saturated with lubricant vapour for a wide range of filter loads and filtration velocities. From the results obtained it can be concluded that loaded industrial filter systems emit air with saturation vapour concentration throughout their operation. Hence, vapour emissions can be estimated easily if the saturation vapour pressure and the mean relative molecular mass are known. Moreover, results obtained from measurements of filters with low loads confirm that the phase transition from liquid to vapour is influenced by the identified process parameters. This is relevant for measurement methods using fibre filters for sampling volatile aerosols. A semi-empirical model to estimate the evaporative losses for low loadings is proposed. However, further research is necessary to determine the full range of parameters that are relevant for evaporative losses from filters loaded with low masses of aerosols.     

A Regional Survey of the Microbiological Water Quality along the Shoreline of the Southern California Bight

A regional survey of the microbiological water quality along the shoreline of the Southern California Bight (SCB), from Point Conception south to Ensenada, Mexico, was conducted during August, 1998, by 36 agencies under the coordination of the Southern California Coastal Water Research Project (SCCWRP). Microbiological water quality was assessed by calculating the percentage of shoreline-mile-days that exceeded bacterial indicator thresholds for total and fecal coliforms, total/fecal ratios, and enterococci. Sample sites were selected using a stratified random sampling approach, with the SCB recreational shoreline divided into six strata: high- and low-use sandy beaches, high- and low-use rocky shoreline, and perennial and ephemeral freshwater outlets. Samples were collected on a weekly basis at a total of 253 sites, beginning on August 2^nd, 1998 and continuing for five weeks. Samples were analyzed by 22 participating labs using their normal methods (multiple tube fermentation, membrane filtration, Colilert® and/or Enterolert®). All labs met testing criteria established through intercalibration exercises and quality control check samples distributed during the sampling period. Nearly 95% of the shoreline-mile days did not exceed daily and monthly bacterial indicator thresholds, demonstrating good bacteriological water quality along the SCB shoreline. Freshwater outlets, comprised mainly of storm drains, had the poorest water quality with 60% and 40% of the shoreline-miles exceeding monthly and daily thresholds, respectively. Freshwater outlets were also more likely to demonstrate exceedances by multiple indicators at a single site, and repeat exceedances at sites over the five-week period. Compared with the southern California beaches, Mexican beaches had nearly 5 times the number of exceedances for total and fecal coliforms, and nearly 8 times the number of exceedances for total/fecal ratios.     

Comparison of PM10 concentrations in high- and medium-volume samplers in a desert environment

The USEPA replaced TSP with PM₁₀ as the National Ambient Air Quality Standard for particulate matter. The commercially available PM₁₀ sampler is a high-volume model using quartz fiber filters. In certain investigations, such as source apportionment studies, chemical analysis of the filter is necessary, however, many analyses cannot be run on quartz filters. An alternate filter such as Teflon is amenable to XRF and ion chemical analyses but is not amenable to analysis for carbon. To overcome these problems DRI constructed a medium-volume PM₁₀ sampler that is capable of collecting particulates on both Teflon and quartz fiber filters simultaneously. This paper describes the design of the DRI medium-volume PM₁₀ sampler, discusses a method for determining equivalence of two samplers, the results of applying the method to test the equivalence of the medium-volume sampler and a commerical high-volume sampler, and examines differences between PM₁₀ and TSP measurements in a southwestern desert.     

浮游动物DNA宏条形码多样性监测采样方法研究

浮游动物是水生生态系统的重要组成部分,对环境因子敏感,是水生生态健康状况的重要指示生物.基于传统形态学的浮游动物调查方法无法鉴定桡足类幼体,难以准确了解浮游动物群落组成.DNA宏条形码技术基于DNA序列差异识别物种,为浮游动物群落组成的准确解析提供了新方法.比较了不同浮游动物采样方法(直接过滤法和网富集法)对浮游动物D...     

Pre-sampling contamination of filters used in measurements of airborne (1 → 3)-β-D-glucan based on glucan-specific Limulus amebocyte lysate assay

Air sampling for (1 → 3)-β-D-glucan may be a good method for assessing inhalation exposure to airborne fungi. Pre-sampling contamination of filter media used for sampling (1 → 3)-β-D-glucan may lead to substantial exposure measurement errors. Using the Limulus amebocyte lysate assay, we tested for pre-sampling levels of (1 → 3)-β-D-glucan on three types of filters-mixed cellulose ester (MCE)[1 brand], glass fiber (GF)[1 brand], and polycarbonate (PC)[5 brands]. Levels of (1 → 3)-β-D-glucan on MCE filters exceeded 4586.1 pg per filter. Levels on GF filters averaged 135.3 (± 28.9) pg per filter (range = 94.8-160.4 pg per filter) and levels on PC filters averaged 152.4 (± 236.1) pg per filter (range = non-detectable-1760.7 pg per filter). Efforts to clean MCE and GF filters were unfeasible or unsuccessful. Sonicating PC filters for two hours in ethanol, followed by a wash in pyrogen-free water, effectively eliminated measured levels of (1 → 3)-β-D-glucan on four brands of PC filters, as compared to untreated PC filters. This pretreatment process did not appear to physically damage the PC filters. Air sampling results highlighted the potentially problematic contamination of untreated PC filters. Ensuring that sampling media are free of (1 → 3)-β-D-glucan before sampling is crucial to accurately measure levels of (1 → 3)-β-D-glucan exposure, especially in environments where levels of (1 → 3)-β-D-glucan are low.     

北方缓流水体水质在线自动监测系统采样口的设计思考

以DO作为水体的污染指标来判定水质类别存在一定的缺陷,北方缓流水体在不同季节常存在不同的DO分层现象,现设在河床底以上0.5米处的自动监测采样口设计缺少科学性。在叙述缓流水体DO特点的同时,介绍一种新的水质在线自动监测采样口的方案,便于类似水体水质自动监测设计中借鉴。     

Filtration of fullerene and copper oxide nanoparticles using surface-modified microfilters

This study evaluated the filtration of engineered nanoparticles of fullerene and copper oxide (CuO) from water by using surface-modified microsized filters. The surfaces of microsized filters of cellulose acetate and glass fibers were coated with cationic and anionic surfactants to give them positively and negatively charged surfaces, respectively. Uncoated microfilters removed 30 % of a fullerene suspension, while no nanosized CuO suspension was removed. Cationic surfactant-coated filters enhanced the removal efficiency up to 70 % for the fullerene suspension, while the anionic surfactant-coated filters could not remove fullerene at all. The positively charged filters with cationic surfactant coating could easily adsorb negatively charged fullerenes on their surfaces. However, none of the surfactant-coated filters removed the CuO nanoparticles because the nanoparticles were not affected by the electrical charge of the filtration medium. The Hamaker constants of nanoparticles interacting with the filter materials in water were calculated to study these interactions. The Hamaker constant of fullerene interacting with cellulose acetate in water, 4.68E???21 J, was higher than that of interacting with quartz in water, 2.59E???21 J. However, the Hamaker constants of CuO interacting with quartz and cellulose acetate in water were both negative values, implying repulsive van der Waals interactions. The curves of potential energy of interaction between nanoparticles and the various filter media implied that the nanoparticles were very stable in water, and so, natural deposition of nanoparticles on the filters would not occur. Therefore, electrical bonding and hydrophobic interactions were the forces dominating fullerene removal by positively charged filters.     

固定源硫酸雾国内外采样方法优劣分析

固定污染源硫酸雾的国标采样方法为滤筒法，但对其采样效率研究较少。在调研国内外标准方法及相关文献的基础上，通过大量实样测定，对国标采样法进行改进：在内装滤筒的烟尘采样管后串联一个冲击式吸收瓶，此改进方法弥补了国标漏测气态硫酸雾的缺陷，采样效率达到99％以上，国标法仅为改进法的47％～68％。将国标改进法与USEPA采样法进行比对，结果表明，由于中国环境本底颗粒物浓度较高，硫酸雾易吸附于颗粒物上，致使USEPA采样效率仅为国标改进法的2?4％～12％。