Detection of metal contamination in wild asparagus near a waste disposal site

Estimating contaminant distributions in environmental media is necesary to evaluate human and ecological hazards. Because of uncertainties in release histories and transport, traditional sampling and statistical techniques applicable to the experimental sciences may not be suitable for exploratory studies at hazardous waste sites. An approach that relies on cluster analysis of principal components (PCA) was used to identify contaminated wild asparagus (Asparagus officinalis) growing in the vicinity of waste disposal sites along the Columbia River at the U.S. Department of Energy's Hanford Site in southeast Washington state. Metals in soil samples taken from the sites contained elevated levels of Ag, Al, Ba, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Zn, and V. Samples of asparagus tissue were collected from the river near the waste site, from Hanford old fields abandoned 52 years ago, and from commercial fields in the neighboring communities. Dried tissues were analyzed for metals content by ICP-mass spectrometry, furnace AA, and cold vapor AA. Tissue concentrations of elements varied over 5 orders of magnitude, from K at 46 900 ppm to As and Ag at maximum concentrations below 1 ppm. PCA produced four components that accounted for 66.2% of the metals variance. Subsequent cluster analysis using Ward's minimum variance separated the data into Columbia River and old-field groups, with the River group further divided into three clusters: plants primarily upriver from the waste sites, plants primarily downriver, and plants growing in or near the waste sites. The clustering showed that the more soluble components of the discharges (Ba and Ca) showed a pattern of distribution in the asparagus plants consistent with the ground water flow pattern, in that these elements were found far downriver of the disposal sites themselves. In contrast, the less mobile elements Al, Cd, Cr, Fe, Mn, Tl, and Zn were elevated only near the most-recently used waste disposal area. Asparagus from agricultural fields, including fields abandoned 50 years ago, contained higher concentrations of Fe, Cu, Pb, K, and Ni than did the wild riverine plants.The U.S. Governments right to retain a non-exclusive royalty free licence in and to any copyright is acknowledged.     

Assessment of plastic waste generation and its potential recycling of household solid waste in Can Tho City, Vietnam

Plastic solid waste has become a serious problem when considering the disposal alternatives following the sequential hierarchy of sound solid waste management. This study was undertaken to assess the quantity and composition of household solid waste, especially plastic waste to identify opportunities for waste recycling. A 1-month survey of 130 households was carried out in Can Tho City, the capital city of the Mekong Delta region in southern Vietnam. Household solid waste was collected from each household and classified into ten physical categories; especially plastic waste was sorted into 22 subcategories. The average household solid waste generation rate was 281.27 g/cap/day. The compostable and recyclable shares respectively accounted for high percentage as 80.74% and 11%. Regarding plastic waste, the average plastic waste generation rate was 17.24 g/cap/day; plastic packaging and plastic containers dominated with the high percentage, 95.64% of plastic waste. Plastic shopping bags were especially identified as the major component, accounting for 45.72% of total plastic waste. Relevant factors such as household income and household size were found to have an existing correlation to plastic waste generation in detailed composition. The household habits and behaviors of plastic waste discharge and the aspects of environmental impacts and resource consumption for plastic waste disposal alternatives were also evaluated.     

Risk assessment near uncontrolled hazardous waste sites: Role of monitoring data

The traditional approach of coupling estimates of human exposures to individual chemicals with laboratory studies of the toxicity of the chemicals as the basis for quantitative assessments of risk is not adequate when considering problems near hazardous waste sites. For example, there are (a) too many chemicals and mixtures involved, (b) containment uncertainties, and (c) future exposure problems associated with groundwater and soil contamination. Among the items to be considered in expanding the dimensions of risk assessment methodologies of the past are (a) identification of chemical groups or of dominant toxic chemicals of principal concern and the likely man-made as well as natural pathways for environmental migration, (b) the role of biological monitoring in addition to traditional monitoring approaches, and (c) the coupling of monitoring data with past, current, and future population activity patterns and with epidemiological and other health data.Monitoring data is a key in risk assessments since there is little likelihood that materials balances or modelling will provide authoritative information concerning exposure levels. The use of monitoring data from control areas and from nationwide baseline surveys in developing comparative risk assessments is particularly important. Finally, recent experience provides us with a number of practical guidelines for designing and carrying out monitoring programs that will provide authoritative and useful data. *** DIRECT SUPPORT *** AZ802019 00002     

Moisture monitoring in waste disposal surface barriers

Surface barriers for waste disposal sites should preventwaste water and gas emission into the environment. It isnecessary to assess their proper operation by monitoring thewater regime of the containment. A set of three new water contentmeasuring devices has been developed that provide an economicalsolution for monitoring the moisture distribution and waterdynamic. They will give an early warning service if the barriersystem is at risk of being damaged. The cryo soil moisture sensor`LUMBRICUS' is an in situ self-calibrating absolute water contentmeasuring device. It measures moisture profiles at spot locationsdown to 2.5 m depth with an accuracy of better than 1.5% and adepth resolution of 0.03 m. The sensor inherently measuresdensity changes and initial cracks of shrinking materials likeclay minerals. The large area soil moisture sensor `TAUPE' is amoisture sensitive electric cable network to be buried in themineral barrier material of the cover. A report will be givenwith results and experiences on an exemplary installation at theWaste Disposal Facility Karlsruhe-West. 800 m² of the barrierconstruction have been continuously monitored since December1997. Volumetric water content differences of 1.5% have beendetected and localised within 4 m. This device is alreadyinstalled in two other waste disposal sites. A modified `TAUPE'was constructed for the control of tunnels and river dams aswell. Thin sheet moisture sensor `FORMI' is specifically designedfor moisture measurements in liners like bentonite, textile andplastic. Due to its flexibility it follows the curvature of theliner. The sensor measures independently from neighbouringmaterials and can be matched to a wide range of differentthickness of the material. The sensors are patented in several countries.     

Distribution of perfluorinated compounds in water, sediment, biota and floating plants in Baiyangdian Lake, China

The distribution of perfluorinated compounds (PFCs) in Baiyangdian Lake, China, was determined in this study. Perfluorooctanoic acid (PFOA) was the dominant PFC in lake water (1.70-73.5 ng L(-1), median 9.72 ng L(-1)), while perfluorooctane sulfonate (PFOS) was the dominant PFC in sediments (0.06-0.64 ng g(-1) dry wt, median 0.19 ng g(-1) dry wt) and in aquatic animals (0.57-13.7 ng g(-1) wet wt, median 2.56 ng g(-1) wet wt). Significant differences in PFC levels were observed among various aquatic animals. We also determined, for the first time, the PFC levels in floating plants, including Ceratophyllum demersum L., Hydrocharis dubia (Bl.) Backer and Salvinia natans (L.), and we found that PFOA and PFNA were the dominant PFCs in these plants. Furthermore, floating plants were observed to have different composition profiles compared to aquatic animals. Geographical differences in PFC levels were also observed, with higher PFC levels in samples from the north part of Baiyangdian Lake than those in the south. The differences in human and industrial activities in different parts of the lake and the discharged wastewater from the Fuhe River may be the major contributors for these geographical differences.     

A method for monitoring ground water quality near waste storage facilities

A practical optimization approach developed in this paper derives effective monitoring configurations for detecting contaminants in ground water. The approach integrates numerical simulation of contaminant transport and mathematical programming. Well sites identified by the methodology can be monitored to establish the occurrence of a contaminant release before a plume migrates to a regulatory compliance boundary. Monitoring sites are established along several horizons located between the downgradient margin of a contaminant source and a compliance boundary. A horizon can form an effective line of defense against contaminant migration to the compliance boundary if it is spanned (covered) by a sufficient number of sites to yield a well spacing that is equal to or less than a maximum value established by numerical modeling. The objective function of the integer programming model formulation expresses the goals of: (1) covering a maximum number of siting horizons, and (2) allocating wells to the single most effective horizon. The latter is determined from well spacing requirements and the width of the zone of potential contaminant migration traversed by the horizon. The methodology employs a highly tractable linear programming model formulation, and the user is not required to predefine a set of potential well sites. These attributes can facilitate its implementation in practice.     

Analysis of multi-temporal landsat satellite images for monitoring land surface temperature of municipal solid waste disposal sites

This studypresents a remote sensing application of using time series Landsat satellite images for monitoring the Trail Road and Nepean municipal solid waste (MSW) disposal sites in Ottawa, Ontario, Canada. Currently, the Trail Road landfill is in operation; however, during the 1960s and 1980s, the city relied heavily on the Nepean landfill. More than 400 Landsat satellite images were acquired from the US Geological Survey (USGS) data archive between 1984 and 2011. Atmospheric correction was conducted on the Landsat images in order to derive the landfill sites’ land surface temperature (LST). The findings unveil that the average LST of the landfill was always higher than the immediate surrounding vegetation and air temperature by 4 to 10 °C and 5 to 11.5 °C, respectively. During the summer, higher differences of LST between the landfill and its immediate surrounding vegetation were apparent, while minima were mostly found in fall. Furthermore, there was no significant temperature difference between the Nepean landfill (closed) and the Trail Road landfill (active) from 1984 to 2007. Nevertheless, the LST of the Trail Road landfill was much higher than the Nepean by 15 to 20 °C after 2007. This is mainly due to the construction and dumping activities (which were found to be active within the past few years) associated with the expansion of the Trail Road landfill. The study demonstrates that the use of the Landsat data archive can provide additional and viable information for the aid of MSW disposal site monitoring.     

Application of the IPCC Waste Model to solid waste disposal sites in tropical countries: case study of Thailand

Measurements of landfill methane emission were performed at nine solid waste disposal sites in Thailand, including five managed sanitary landfills (four deep and one shallow landfills) and four unmanaged landfills (three deep and one shallow dumpsites). It was found that methane emissions during the rainy season were about five to six times higher than those during the winter and summer seasons in the case of managed landfills and two to five times higher in the case of unmanaged landfills. Methane emission estimate using the Intergovernmental Panel on Climate Change (IPCC) Waste Model was compared with the actual field measurement from the studied disposal sites with methane correction factors and methane oxidation factors that were obtained by error function analysis with default values of half-life parameters. The methane emissions from the first-order decay model from the IPCC Waste Model yielded fair results compared to field measurements. The best fitting values of methane correction factor were 0.65, 0.20, 0.15, and 0.1 for deep landfills, shallow landfills, deep dumpsites, and shallow dumpsites, respectively. Using these key parameters in the case of Thailand, it was estimated that 89.22 Gg of methane were released from solid waste disposal sites into the atmosphere in 2006.     

Municipal solid waste management in Thailand and disposal emission inventory

The increasing municipal solid waste (MSW) generation along with the high fraction of organic waste and a common disposal of open dumping is the current scenario in many areas in Thailand. As a response to this problem, the country’s Pollution Control Department (PCD) aims to reduce the MSW generation rate to less than 1 kg/capita/day, increase the collection efficiency, and improve the recovery of recyclables. For many years, more than 60% of the solid waste disposal system in Thailand has been carried out by open dumping. According to the survey conducted by this study, in 2004 there were 425 disposal sites (95 landfills; 330 open dumps) in Thailand and an estimated methane emission of 115.4 Gg/year was generated based on this practice. It has been estimated that the anticipated methane emission in Thailand will rise from 115.4 Gg/year to 118.5 Gg/year if the largest open dumpsites in provinces with no existing landfill are upgraded to sanitary landfill; and it will increase to 193.5 Gg/year if the existing sanitary landfill is upgraded to integrated waste management facilities. Moreover, Bangkok metropolitan have the highest methane emission (54.83 Gg/year) among all the regions in Thailand. The methane emission forecast of 339 Gg/year by 2020 (based on LandGEM methodology) provides a stimulus to create a comprehensive plan to capture and utilize methane as an energy source.     

气相色谱法测定水和废水中丙烯腈

本文通过采用气相色谱法,以ＧＤＸ－５０２为固定相,ＦＩＤ为检测器测定水和废水中的丙烯腈,精密度和回收率高．方法简便易行,能满足行业废水和地面水的监队是水和废水中丙烯腈分析的较理想方法。     

Greenhouse gas emission reductions through waste management and disposal planning

The Third Conference of the Parties of the UN-FCCC (CoP-3) held in Kyoto in 1997 defined a Protocol with level of reduction of the Greenhouse Gasses (GHGs) overall emissions for Italy of 6.5% with respect to 1990 emissions. A mathematical model was created in order to evaluate the range of GHGs reduction effects obtained by upgrading waste collection, treatment and disposal system to new Italian regulation. This revised version was published online in July 2006 with corrections to the Cover Date.     

Uptake of arsenic by alkaline soils near alkaline coal fly ash disposal facilities

The attenuation of arsenic in groundwater near alkaline coal fly ash disposal facilities was evaluated by determining the uptake of arsenic from ash leachates by surrounding alkaline soils. Ten different alkaline soils near a retired coal fly ash impoundment were used in this study with pH ranging from 7.6 to 9.0, while representative coal fly ash samples from two different locations in the coal fly ash impoundment were used to produce two alkaline ash leachates with pH 7.4 and 8.2. The arsenic found in the ash leachates was present as arsenate [As(V)]. Adsorption isotherm experiments were carried out to determine the adsorption parameters required for predicting the uptake of arsenic from the ash leachates. For all soils and leachates, the adsorption of arsenic followed the Langmuir and Freundlich equations, indicative of the favorable adsorption of arsenic from leachates onto all soils. The uptake of arsenic was evaluated as a function of ash leachate characteristics and the soil components. The uptake of arsenic from alkaline ash leachates, which occurred mainly as calcium hydrogen arsenate, increased with increasing clay fraction of soil and with increasing soil organic matter of the alkaline soils. Appreciable uptake of arsenic from alkaline ash leachates with different pH and arsenic concentration was observed for the alkaline soils, thus attenuating the contamination of groundwater downstream of the retired coal fly ash impoundment.     

Occurrence of perfluorinated compounds in the aquatic environment as found in science park effluent,river water,rainwater, sediments,and biotissues

The current article maps perfluoroalkyl acids (PFAAs) contamination in the largest Science Park of Taiwan. The occurrence of ten target PFAAs in the effluent of an industrial wastewater treatment plant (IWWTP), its receiving rivers, rainwater, sediment, and the muscles and livers of fish was investigated. All target PFAAs were found in effluent of IWWTP, in which perfluorooctane sulfonate (PFOS) (6,930 ng/L), perfluorohexyl sulfonate (PFHxS) (2,662 ng/L) and perfluorooctanoic acid (PFOA) (3,298 ng/L) were the major constituents. Concentrations of PFBS and PFOS in the IWWTP downstream areas have exceeded safe concentration levels of avian and aquatic life, indicating a potential risk to wildlife in those areas. In sediment samples, predominant contaminants were PFOS (1.5–78 ng/g), PFOA (0.5–5.6 ng/g), and perfluorododecanoic acid (PFDoA) (nd–5.4 ng/g). In biological tissue samples, concentrations as high as 28,933 ng/g of PFOS were detected in tilapia and catfish liver samples. A positive correlation for log (C _sediment/C _water) and log (C _tissue/C _water) was found. The concentration and proportion (percentage of all PFAAs) of PFOS found in biotissue samples from the Keya River (which receives industrial wastewater) were found to be much greater (200 times) than those of samples from the Keelung River (which receives mainly domestic wastewater). These findings suggest that the receiving aquatic environments and, in turn, the human food chain can be significantly influenced by industrial discharges.     

甲萘酚显色光度法测定水中苯胺

对甲萘酚偶氮显色光度法测定水中苯胺的方法进行了验证性研究。结果表明,该方法具有简单、快速、稳定等优点。线性区间在0.05～5.5mg/L范围内,相关系数等于0.9997,苯胺浓度小于0.05mg/L或大于5.5mg/L时,测量误差比较大。还考察了NaCl、KCl、NaNO_3、KNO_3、Na_2SO_4、K_2SO_4、TiO_2、ZnO,苯酚,以及由吐温-80/苯/水/正丁醇组成的O/W微乳液对测量的影响。     

A pilot study on the determination of perfluorooctanesulfonate and other perfluorinated compounds in blood of Canadians

A pilot study was conducted to provide preliminary data on the concentrations of perfluorooctanesulfonate (PFOS), perfluorooctanoic acid (PFOA) and perfluorooctanesulfonamide (PFOSA) in the blood of Canadians. A set of 56 human serum samples was collected from non-occupationally exposed Canadians and analyzed by microbore HPLC-negative ion electrospray tandem mass spectrometry. PFOS was the main component of perfluorinated organic compounds (PFCs) and was detected in all 56 blood specimens at an average concentration of 28.8 ng mL(-1) and a range from 3.7 to 65.1 ng mL(-1). The concentration of PFOA was an order of magnitude lower than that of PFOS and was found only in 16 samples (29%) at concentrations above the limit of quantification (LOQ). PFOSA was not detected at levels above the method detection limit (MDL) in any of the samples. The levels of PFCs observed in the sample group of non-occupationally exposed humans in Canada were similar to the levels reported in a previous US study with a similar sample pool size. Two distinct PFOS isomers in human serum were identified by accurate mass determination.     

Sampling and analyses of colloids at the Drigg low level radioactive waste disposal site

Water samples have been extracted from inside (from standpipes) and from outside (from boreholes) of the trenches at the low level radioactive waste disposal site at Drigg in Cumbria, UK. The samples were taken anaerobically from between 8.5 and 10.0 m below the surface using a submersible pump at low flow rates to ensure that the waters in the standpipes and boreholes were maintained at constant levels. To ensure representative samples, the Eh, pH. conductivity, temperature, iron and dissolved oxygen concentrations of the waters were taken during initial purging and during sampling. The gross tritium, gross non-tritium beta, gross alpha and gamma activities of each sample were determined using suitable sample preparation and counting techniques. Samples were then anaerobically, sequentially filtered through 12 microm, 1 microm, 30 kDa and 500 Da filter membranes. The filtrates were analysed for gross alpha, gross non-tritium beta and gamma activities. SEM and STEM analyses were used to determine the colloid population. An energy dispersive analyser on the SEM was used to determine the major elements present in the colloids. UV-visible spectrophotometry, fluorescence spectrophotometry and high performance size exclusion liquid chromatography were used to analyse the waters before and after treatment with ion exchange materials to determine whether natural organic matter was present in the waters. Results showed that two major types of colloids (iron containing colloids and silicon containing colloids) were present in the waters. There were also a small number of other colloids that contain, as major elements, aluminium, calcium and chromium. Organic colloids were also present. The majority of the radioactivity in the waters was due to tritium. Waters taken from outside the trenches contained low levels of non-tritium beta activities and alpha activities which were lower than the minimum detectable amount. Waters taken from the trenches contained non-tritium beta activities and low levels of alpha emitters. Filtration of the trench waters showed that some of the alpha activity was retained by the 30 kDa and 500 Da membranes suggesting that this activity was associated with small colloids. Radioactivity was not found to be associated with colloids present in the waters taken from outside the trenches. Possible reasons for this observation could be that radionuclide bearing colloids have not yet reached the far-field or that the radionuclide concentration is diluted to below the minimum detectable amount. After concentrating two of the samples by factors of x20 and x 16 respectively, 2.4+/-0.1 and 0.6+/-0.1 Bq dm(-3) of 137Cs were measured.     

火焰原子吸收光谱法测定工业废水中铊

研究了火焰原子吸收光谱法测定工业废水中铊。检出限 (3 σ)为 0 5mg L,相对标准偏差小于 2 0 % ,回收率在92 %～ 1 0 6 %范围 ,方法简便快速。