Pilot scale application of a method for the analysis of perfluorinated compounds in surface soils

A growing number of studies now indicate that perfluorinated compounds (PFCs) are globally distributed in the environment. Their widespread distribution and presence in remote locations has led to questions about the importance of atmospheric and oceanic transport. Describing their distribution in surface soils is also an essential but neglected element in developing a comprehensive understanding of their occurrence in the environment. Soils are the critical link between global atmospheric and hydrologic processes where both local and distant contaminants can accumulate and be released into aquatic and terrestrial communities. Because PFC concentrations in soils will influence ground and surface water, wildlife, and crops, methods to accurately measure PFCs in soil are clearly needed. To help answer this need, we developed a method for the analysis of nine perfluorinated carboxylic acids and four perfluorinated sulfonic acids in soil. Samples from six nations (n = 10 per nation) were analyzed by LC-MS/MS to demonstrate the method performance parameters and to make preliminary observations about the occurrence of the PFCs in soils in different parts of the world. The resulting method shows acceptable performance characteristics for the target compounds in most soils while documenting the widespread occurrence of PFCs in surface soils.     

Distribution and temporal changes of lead in the surface seawater in the western Pacific and adjacent seas derived from coral skeletons

We determined Pb contents together with Pb isotopic compositions in coral skeletons (Porites spp.) collected from the western Pacific and adjacent seas to examine distribution of Pb in sea surfaces. Temporal records of Pb were also investigated using coral skeletons from Hainan and Ogasawara Island, located in China and Japan, respectively. The spatial distribution of Pb showed a clear dilution pattern of Pb from Asian continent to the open ocean. Also the similar trend was found in the Java Sea from Jakarta to the offshore. In addition to the spatial distribution, Pb contents in Ogasawara coral have gradually increased during last 108 years. It may be attributed to Pb emission mainly from industrial activities in Asian countries. Hainan coral, which provided 10 years record of Pb, showed a remarkable decline around 1997 probably due to the partial introduction of unleaded gasoline in China.     

Statistical approach for the source identification of boron in leachates from industrial landfills

Boron has been found in high concentrations in leachates from landfills located throughout Japan. However, the source(s) of boron in the leachates, i.e., what kind of waste(s) releases this element into the leachate, has not been clarified. In this study, boron concentrations in leachates from 48 industrial landfills were evaluated, in relation to the categories of waste constituting the landfill in each of the sites, by multiple regression analysis. The multiple regression analyses were carried out using the log-transformed boron concentration as a dependent variable and each of 19 categories of industrial waste (according to the Japanese Waste Disposal and Public Cleansing Law) as independent variables. Stepwise variable selection was employed in the analyses. Although the significant variable(s) selected varied according to the data sets analyzed (viz., data sets from least controlled landfill sites, from controlled landfill sites, and from both), cinders, slag, and waste plastics emerged as wastes with positive partial regression coefficients that significantly explained the boron levels in the leachates. These results indicated that cinders, slag, and waste plastics were the sources of high concentrations of boron in the leachates. The results of the present exploratory statistical analyses warrant a systematic survey of the boron contents of, and leachability from, cinders, slag, and waste plastics. Received: January 17, 2000 / Accepted: July 24, 2000     

Evaluation of the impact of matrix effects in LC/MS measurement on the accurate quantification of neonicotinoid pesticides in food by isotope-dilution mass spectrometry

The use of isotope-labeled internal standards is the most widely accepted approach to overcome the matrix effects on quantification of pesticides in food by LC/MS. We evaluated the impact of the matrix effects on quantification of six neonicotinoid pesticides, acetamiprid, clothianidin, dinotefuran, imidacloprid, thiacloprid, and thiamethoxam, in food by using deuterated internal standards. The calibration curves for each pesticide were obtained by using matrix-free and matrix-matched calibration solutions with blank brown rice, carrot, and green onion extracts. For brown rice and carrot, the matrix effects were not observed. In contrast, the slopes of calibration curves for each pesticide were influenced by presence of green onion extracts in calibration solutions (variability of the slopes was 4–9%), because the ratios of peak area for native pesticide to those for internal standards were influenced by matrix. The spike-and-recovery test with green onion was also performed. The analytical values obtained by using matrix-free calibration solution were biased from the spiked concentration, whereas those obtained by using matrix-matched calibration solution were comparable to the spiked concentration. These results indicate that matrix-matched calibration solution should be used for accurate quantification of neonicotinoid pesticides in food by LC/MS using deuterated internal standards.     

Urinary concentrations of organophosphorus insecticide metabolites in Japanese workers

A recent development in analytical chemistry has enabled us to monitor systemic organophosphorus insecticide (OP) exposure at individual levels. At present, however, limited data are currently available on urinary OP metabolite levels worldwide. The purpose of this study was to assess urinary dialkylphosphate (DAP) concentrations in Japanese workers. Urine samples were collected in both summer and winter from 339 Japanese adults who worked as food distributors (FDs, n = 164), apple farmers (AFs, n = 147) and pest control operators (PCOs, n = 28). DAPs were measured by gas chromatography-mass spectrometry after derivatization with pentafluorobenzylbromide. Dimethylphosphate (DMP), diethylphosphate (DEP), dimethylthiophosphate (DMTP) and diethylthiophosphate (DETP) were detected in the urine of over 87% of the studied populations in both seasons. The geometric mean values of total DAPs (nmol g⁻¹ creatinine), DMP, DMTP, DEP and DETP (μg g⁻¹ creatinine) in summer and winter were 106.7 and 98.3, 7.0 and 3.8, 3.4 and 4.5, 0.8 and 1.5, and 0.3 and 0.2 for the FDs, 440.8 and 197.7, 33.1 and 10.8, 10.1 and 5.8, 4.2 and 4.7 and 1.6 and 0.8 for the AFs, and 473.4 and 284.6, 28.9 and 22.2, 17.6 and 4.6, 3.5 and 4.4, and 0.5 and 0.6 for the PCOs, respectively, thereby revealing significantly higher concentrations in AFs and PCOs groups than in the FDs in both seasons except for winter DMTP. These DAP concentrations were approximately the same or at lower levels compared with those reported in the previous literature. This is one of the first studies to demonstrate urinary DAP concentrations in Japanese adults.     

日本优良产业废弃物处理企业认定制度简介

日本优良产业废弃物处理企业的认定制度是由都道府县知事·政令市长对产业废弃物处理行业中符合“优良标准”的企业进行认定,被认定的“优良认定企业”可享有产业废弃物处理行业许可的有限期限由通常的5年延长到7年等的优惠政策.     

Arsenic speciation for the phytoremediation by the Chinese brake fern, Pteris vittata

Arsenic(As)speciation for the phytoremediation by the Chinese brake fern was studied.In particular,the mechanism of how plants induce compounds containing thiol(SH)and proteins by As exposure in terms of the relationship between As and phosphate uptaken into plant cells was examined.Pteris vittata callus could effciently reduce As(V)to As(III)by the rapid introduction of reductase and synthesize thiols leading to phytochelatins production.Furthermore,Pteris vittata could control phosphate concentration in t...     

Investigation into the relationship between major and minor element contents and particle size and leachability of boron in fly ash from coal fuel thermal power plants

A basic investigation of boron in discharged fly ash by coal fuel thermal power plants in several worldwide locations was carried out. Eight kinds of fly ash sample were prepared from eight coal fuel thermal power plants. Two of the fly ash samples were used to examine the relationship between the concentration of boron in fly ash and the particle size. When the particle size of fly ash is smaller, there is a possibility that it will be released into the air and spread over a wide area in the environment. However, it has become apparent that fly ash of smaller particle size has a higher concentration of boron and a higher enrichment factor. In other fly ash samples, the boron contents were examined and leaching tests were carried out. There is acidic fly ash as well as alkaline fly ash that contains larger amounts of acidic or basic salts. On alkaline fly ash, when the concentration of boron bound to Fe-Mn oxide is low; it has become apparent that leaching boron is increased in a solution with lower pH of approximately 4 which is nearly the pH of acid rain.     

Atmospheric mercury emissions from waste combustions measured by continuous monitoring devices

Atmospheric mercury emissions have attracted great attention owing to adverse impact of mercury on human health and the ecosystem. Although waste combustion is one of major anthropogenic sources, estimated emission might have large uncertainty due to great heterogeneity of wastes. This study investigated atmospheric emissions of speciated mercury from the combustions of municipal solid wastes (MSW), sewage treatment sludge (STS), STS with waste plastics, industrial waste mixtures (IWM), waste plastics from construction demolition, and woody wastes using continuous monitoring devices. Reactive gaseous mercury was the major form at the inlet side of air pollution control devices in all combustion cases. Its concentration was 2.0–70.6 times larger than elemental mercury concentration. In particular, MSW, STS, and IWM combustions emitted higher concentration of reactive gaseous mercury. Concentrations of both gaseous mercury species varied greatly for all waste combustions excluding woody waste. Variation coefficients of measured data were nearly equal to or more than 1.0. Emission factors of gaseous elemental mercury, reactive gaseous mercury, and total mercury were calculated using continuous monitoring data. Total mercury emission factors are 0.30 g-Hg/Mg for MSW combustion, 0.21 g-Hg/Mg for STS combustion, 0.077 g-Hg/Mg for STS with waste plastics, 0.724 g-Hg/Mg for industrial waste mixtures, 0.028 g-Hg/Mg for waste plastic combustion, and 0.0026 g-Hg/Mg for woody waste combustion. All emission factors evaluated in this study were comparable or lower than other reported data. Emission inventory using old emission factors likely causes an overestimation.

Implications Although waste combustion is one of major anthropogenic sources of atmospheric mercury emission, estimated emission might have large uncertainty due to great heterogeneity of wastes. This study investigated speciated mercury emissions from the combustions of municipal solid wastes, sewage treatment sludge with/without waste plastics, industrial waste mixtures, waste plastics from construction demolition, and woody wastes using continuous monitoring devices. Reactive gaseous mercury was the major form in all combustion cases and its concentration in the gas had large fluctuation. All emission factors evaluated in this study were comparable or lower than other reported data. Emission inventory using old emission factors likely causes an overestimation.