Investigation of Urinary Metabolites of Organophosphate Esters in Hanoi, Vietnam: Assessment Exposure and Estimated Daily Intake.

In recent years, organophosphate esters (OPEs) have become one of the most common additives in various consumer products worldwide, therefore the exposure and impact of OPEs on human health are drawing a lot of attention. In this study, three metabolites of OPEs including bis(1,3-dichloro-2-propyl) phosphate (BDCIPP), diphenyl phosphate (DPhP) and diethyl phosphate (DEP) were investigated in first-morning void urine samples taken from a population (age range: 3-76 years old) in Hanoi, Vietnam. The most dominant urinary OPE metabolite was DEP with the geometric mean of specific gravity adjust (SG-adjusted) concentration were 1960 ng mL-1 and detected frequency (DF) of 98%. Followed by DPhP (8.01 ng mL-1, DF: 100%) and BDCIPP (2.18 ng mL-1, DF: 51%). The results indicated that gender and age might have associations with the OPE metabolites variation in urine samples. The levels of OPE metabolites in urine samples from females were slightly higher than in males. An increase in age seems to have an association with a decrease in DPhP levels in urine. Exposure doses of parent OPEs were evaluated from the unadjusted urinary concentration of corresponding OPE metabolite. The estimated exposure doses of triethyl phosphate (TEP) (mean: 534,000 ng kg-1 d-1) were significantly higher than its corresponding reference dose, suggesting the high potential risk from the current exposure doses of TEP to human health. The results of this work provided the initial information on the occurrence of three OPE metabolites in urine from Hanoi, Vietnam and estimated exposure dose of corresponding parent OPEs.

Occurrence and risk of human exposure to organophosphate flame retardants in indoor air and dust in Hanoi, Vietnam.

The presence and distribution of thirteen organophosphate flame retardants (OPFRs) were investigated in indoor air and dust samples collected in Hanoi, Vietnam. The total OPFRs (Æ©OPFRs) concentrations in indoor air and dust samples were 42.3-358 ng m-3 (median 101 ng m-3) and 1290-17,500 ng g-1 (median 7580 ng g-1), respectively. The profile of OPFRs in both indoor air and dust indicated that tris(1-chloro-2-propyl) phosphate (TCIPP) was the most dominant compound with a median concentration of 75.3 ng m-3 and 3620 ng g-1, contributing 75.2% and 46.1% to Æ©OPFRs concentrations in indoor air and dust, respectively, followed by tris(2-butoxyethyl) phosphate (TBOEP), with a median concentration of 16.3 ng m-3 and 2500 ng g-1, contributing 14.1% and 33.6% to Æ©OPFRs concentrations in indoor air and dust, respectively. The levels of OPFRs in the indoor air samples and corresponding indoor dust samples showed a strong positive correlation. The total estimated daily intakes (EDItotal) of Æ©OPFRs (via air inhalation, dust ingestion, and dermal absorption) for adults and toddlers under the median and high exposure scenarios were 36.7 and 160 ng kg-1 d-1, and 266 and 1270 ng kg-1 d-1, respectively. Among the investigated exposure pathways, dermal absorption was a primary exposure pathway to OPFRs for both toddlers and adults. The hazard quotients (HQ) ranged from 5.31 × 10-8 to 6.47 × 10-2 (<1), and the lifetime cancer risks (LCR) were from 2.05 × 10-11 to 7.37 × 10-8 (<10-6), indicating that human health risks from exposure to OPFRs in indoor environments are not significant.

Occurrence and ecological risk assessment of organophosphate esters in surface water from rivers and lakes in urban Hanoi, Vietnam.

In this study, an investigation on the pollution status, distribution, and ecological risk to the aquatic organisms of six organophosphate tri-esters (tri-OPEs) and two organophosphate tri-esters (di-OPEs) in surface water in urban Hanoi, Vietnam were conducted. In 37 surveyed water samples (6 rivers and 17 lakes), all eight targeted OPEs were discovered with a detection frequency (DF) of 41-100% and the concentration varied largely from below the method detection limit (

Academic performance warning system based on data driven for higher education.

Academic probation at universities has become a matter of pressing concern in recent years, as many students face severe consequences of academic probation. We carried out research to find solutions to decrease the situation mentioned above. Our research used the power of massive data sources from the education sector and the modernity of machine learning techniques to build an academic warning system. Our system is based on academic performance that directly reflects students' academic probation status at the university. Through the research process, we provided a dataset that has been extracted and developed from raw data sources, including a wealth of information about students, subjects, and scores. We build a dataset with many features that are extremely useful in predicting students' academic warning status via feature generation techniques and feature selection strategies. Remarkably, the dataset contributed is flexible and scalable because we provided detailed calculation formulas that its materials are found in any university or college in Vietnam. That allows any university to reuse or reconstruct another similar dataset based on their raw academic database. Moreover, we variously combined data, unbalanced data handling techniques, model selection techniques, and research to propose suitable machine learning algorithms to build the best possible warning system. As a result, a two-stage academic performance warning system for higher education was proposed, with the F2-score measure of more than 74% at the beginning of the semester using the algorithm Support Vector Machine and more than 92% before the final examination using the algorithm LightGBM.

Occurrence, potential sources, and risk assessment of pharmaceuticals and personal care products in atmospheric particulate matter in Hanoi, Vietnam.

Pharmaceutical and personal care products (PCPPs) were recently recognized as emerging pollutants due to their potential for adverse health and environmental impacts. One potential route of exposure, atmospheric particulate matter (APM), for polar PPCP chemicals has to date received limited attention. This study screened for 190 polar PPCP chemicals in outdoor APM samples collected from two locations in Hanoi, Vietnam, and predictions of source and potential effects on human health are presented. Day and night, as well as dry and rainy seasonal samples, were taken, and samples screened by LC-TOF, using sequential window acquisition and all theoretical fragment ion spectra method. Eleven PPCP chemicals were detected above the LOD and in more than one sample. The ∑11PPCP chemicals ranged from 0.61 to 21.9 ng m-3 (median 2.07 ng m-3), with between 2 and 6 compounds identified in individual samples (median 4). The ∑11PPCP chemicals collected near a heavy traffic area was greater than that in a populated residential zone. Night concentrations were significantly greater than day in both dry and rainy seasons (p < 0.05). Butyl methoxydibenzoylmethane, benzophenone-3, acetaminophen, cotinine, and fluorescent brightener 71 were detected in > 50% of samples. These are typically found in sunscreens, cosmetics, antipyretics, tobacco, and dyes. The DIair, hazard quotient (HQ), and hazard index (HI) for adults and children at sampling sites were estimated. The HQ for both adults and children were orders of magnitude less than the risk or were close to or whichever. APM does appear to be a potential additional secondary exposure source of PPCP chemicals to the environment and more work is needed to identify if sources are local or ubiquitous and if there is a greater health risk.

Sediment contamination with polybrominated diphenyl ethers and alternative brominated flame retardants: case study in urban lakes of Hanoi, Vietnam.

Information regarding the contamination of brominated flame retardants (BFRs) in lake sediments from Vietnam and Southeast Asia is still very limited. To fill such knowledge gaps, surface sediment samples from five urban lakes in Hanoi, Vietnam, were analyzed for polybrominated diphenyl ethers (PBDEs) and some other BFRs. Concentrations of total PBDEs ranged from 1.1 to 26 (median 6.6) ng/g dry weight with the most predominant congeners as BDE-209 (62 ± 17%), BDE-99 (10 ± 8%), and BDE-47 (6 ± 5%). Concentrations of other BFRs decreased in the order: decabromodiphenyl ethane (DBDPE) > 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE) > hexabromobiphenyl (BB-153) > pentabromoethylbenzene (PBEB), which were about one to two orders of magnitude lower than PBDEs. BDE-209 and DBDPE were highly correlated (Pearson's r = 0.879; p < 0.01), suggesting their similar applications and/or environmental fate. Potential sources of BFRs in lake sediments are estimated to be wastewater discharge, riverine inflow, and atmospheric deposition.

Occurrence and risk assessment of herbicides and fungicides in atmospheric particulate matter in Hanoi, Vietnam.

Vietnam is a Southeast Asian developing country with rapidly increasing air pollution, especially in large cities. Over 350,000 chemicals and chemical mixtures are produced and used in Vietnam; however, the country has only implemented air quality standards for 44 substances, which are primarily focused on inorganic and volatile organic compounds. Although numerous pesticides are frequently applied across large cities in Vietnam, information on their concentrations in atmospheric particulate matter (APM) is limited. Therefore, to investigate their occurrence and health effects, 187 pesticides in APM were screened using the liquid chromatography-mass spectrometry-quadrupole time of flight- Sequential Window Acquisition of All Theoretical Fragment Ion Spectra method (LC-QTOF-MS-SWATH). A total of 22 pesticides (16 fungicides and 6 herbicides) were quantified in the dry and rainy seasons. Among them, 19 substances were quantified in APM for the first time in Vietnam. Their median total concentrations in the dry season were higher than those in the rainy season, and the concentrations in the daytime were one-third of the night-time concentrations in both seasons. Their total levels ranged from 0.82 to 21.1 ng m-3 (median, 3.63 ng m-3), the detection frequencies of 9 pesticides were higher than 70%, and 7-14 pesticides were detected per sample (median, 10). Some of the detected pesticides were likely sourced from their prevalent use in amenity turf protection (e.g., in parks and public roads) and weed control (e.g., in gardens, floriculture, and agriculture). The total daily intake (DIair) values for adults, children, and infants were 8.17E-06, 2.06E-05, and 2.45E-05 mg kg-1 d-1, respectively, and the highest Hazard Quotients (HQs) were 4.81E-04, 1.22E-03, and 1.44E-03, respectively. All HQs and HIs of the pesticides were < 1 for all population groups (adults, children, and infants), indicating negligible exposure risks.

Contamination status, emission sources, and human health risk of brominated flame retardants in urban indoor dust from Hanoi, Vietnam: the replacement of legacy polybrominated diphenyl ether mixtures by alternative formulations.

This study investigated the occurrence, distribution of several additive brominated flame retardants (BFRs) such as polybrominated diphenyl ethers (PBDEs) and some novel brominated flame retardants (NBFRs) in urban indoor dust collected from ten inner districts of Hanoi, Vietnam to assess the contamination status, emission sources, as well as their associated human exposure through indoor dust ingestion and health risks. Total concentrations of PBDEs and NBFRs in indoor dust samples ranged from 43 to 480 ng g-1 (median 170 ng g-1) and from 56 to 2200 ng g-1 (median 180 ng g-1), respectively. The most abundant PBDE congener in these dust samples was BDE-209 with concentrations ranging from 29 to 360 ng g-1, accounting for 62.6-86.5% of total PBDE levels. Among the NBFRs analyzed, decabromodiphenyl ethane (DBDPE) was the predominant compound with a mean contribution of 98.6% total NBFR amounts. Significant concentrations of DBDPE were detected in all dust samples (median 180 ng g-1, range 54-2200 ng g-1), due to DBDPE as a substitute for deca-BDE. Other NBFRs such as 1,2-bis(2,4,6-tribromophenoxy) ethane (BTBPE), pentabromoethylbenzene (PBEB) and 2,2',4,4',5,5'-hexabromobiphenyl (BB-153) were found at very low levels. Based on the measured BFR concentrations, daily intake doses (IDs) of PBDEs and NBFRs via dust ingestion at exposure scenarios using the median and 95th percentile levels for both adults and children were calculated for risk assessment. The results showed that the daily exposure doses via dust ingestion of all compounds, even in the high-exposure scenarios were also lower than their reference dose (RfD) values. The lifetime cancer risks (LTCR) were much lower than the threshold level (10-6), which indicated the acceptable health risks resulting from indoor BFRs exposure for urban residents in Hanoi.

Comprehensive study of insecticides in atmospheric particulate matter in Hanoi, Vietnam: Occurrences and human risk assessment.

Air pollution is the most serious environmental issue in Vietnam, particularly in big cities. Air pollutants that are set as environmental standards are regularly monitored by the public institutions. Whereas, environmental data on organic micro-pollutants in atmospheric particulate matters (APMs) is limited, including PAHs and POPs. Although massive pesticides are used in big cities, their data in APMs in Vietnam is very scarce. In order to elucidate their occurrence in the ambient air in Hanoi and their health effects, we surveyed 107 insecticides in APMs by a novel target screening method using LC-QTOF-MS-SWATH. A total of 19 insecticides were detected in the dry and the rainy seasons. Among them, 16 substances are, to our knowledge, reported for the first time in the literature. Their total concentrations varied from 0.47 to 27.0 ng m-3 (median, 3.6 ng m-3), detection frequencies of 12 compounds are higher than 42%, and the number of insecticides detected per each sample ranging from 5 to 13 (median, 9). Total concentrations in the dry season were generally higher than in the rainy season, and concentrations at night were higher than daytime in both seasons. The level of insecticides depends not only on the season, but also on its physicochemical properties, its application conditions, and the meteorological conditions. Their emission sources could be related to agricultural usage, floricultural activities, and pest control in houses. The total maximum daily intake (DIair) through inhalation for adults and children were 2.39E-05 mg kg-1 d-1 and 2.98E-05 mg kg-1 d-1, respectively. The highest Hazard Quotients (HQs) were 1.34E-03 and 3.37E-03, and the highest Hazard Indices (HIs) were 2.71E-03 and 6.33E-03 for adults and children, respectively. All values of HQs, and HIs of insecticides were less than 1, indicating that health risk would be negligible.

Comprehensive Study of Organic Micro-pollutants in Flooded Paddy Soils in Central Vietnam: Levels, Pollution Pathways and Sources.

In order to assess the environmental impacts caused by flood to the paddy field, 940 semi-volatile organic compounds (SVOCs) were screened in paddy soil samples taken in central Vietnam before and after flooding. The concentration of 166 SVOCs in soil samples ranged from 0.031 to 2241 (mean 89.1) µg kg-1 dry wt. Chemicals originating from household sources showed the highest level, followed by chemicals originating from agriculture. Since untreated domestic wastewater used for agricultural irrigation, organic micro-pollutants in domestic wastewater is the main source of pollutants in paddy soil. However, contamination levels of pollutants in paddy soil after flooding were lower than those before flooding, possibly due to the removal of pollutants by floodwater. As a result, pollution characteristic of pollutants at sampling locations were different before flooding while they became similar after flooding due to the dispersion and elution of organic pollutants from soil into floodwaters.

Target screening analysis of 970 semi-volatile organic compounds adsorbed on atmospheric particulate matter in Hanoi, Vietnam.

Vietnam's rapid economic development has resulted in dramatic increases in construction and the number of transportation vehicles. There is now growing public concern regarding increasing air pollution, especially in big cities; however, little information is available on air quality, particularly regarding semi-volatile organic compounds (SVOCs) adsorbed on atmospheric particulate matter. Here, we determined the frequency and concentrations of 970 SVOCs in 48 air particle samples collected by means of high-volume air sampling in Hanoi, Vietnam, by using a target screening method and a gas chromatography-mass spectrometry database. A total of 118 compounds (12.2% of the target compounds) were detected at least once in the samples, and the number of chemicals detected in each sample ranged from 85 to 103 (median, 92). For samples collected near a heavily trafficked road, the concentrations of target compounds in the samples were higher in samples collected during the day than in those collected at night, whereas the opposite was true for samples collected in a highly populated residential area with industrial activities related to the production of fresh noodles. Sixteen PAHs were detected at high concentrations in nearly 100% of the samples. Eighteen pesticides were detected, with permethrin being detected the most frequently (>70% samples), which can be explained by the use of permethrin-based Permecide 50 EC for dengue fever control during the sampling period. Endocrine-disrupting chemicals (i.e., bisphenol A, 4-nitrophenol) and pharmaceuticals and personal care products (diethyltoluamide, caffeine) were detected in over 90% of the samples. Seven sterols, five phthalate compounds and five organophosphorus flame retardants were detected in the samples. This is the first comprehensive survey of SVOCs adsorbed on atmospheric particulate matter in Vietnam, and as such, this study provides important new information about the frequency and concentrations of atmospheric SVOC contamination. The variety of chemicals detected in this study implies an abundance of pollution sources; further investigations to determine these pollution sources and the risks posed by the detected SVOCs to human health are warranted.

Simultaneous effect of dissolved organic carbon, surfactant, and organic acid on the desorption of pesticides investigated by response surface methodology.

Desorption of pesticides (fenobucarb, endosulfan, and dichlorodiphenyltrichloroethane (DDT)) from soil to aqueous solution with the simultaneous presence of dissolved organic carbon (DOC), sodium dodecyl sulfate (SDS), and sodium oxalate (Oxa) was investigated in batch test by applying a full factorial design and the Box-Behnken response surface methodology (RSM). Five concentration levels of DOC (8 to 92 mg L-1), SDS (0 to 6.4 critical micelle concentration (CMC)), and Oxa (0 to 0.15 M) were used for the experiments with a rice field topsoil. The results of RSM analysis and analysis of variance (ANOVA) have shown that the experimental data could be well described by quadratic regression equations with determination coefficients (R 2) of 0.990, 0.976, and 0.984 for desorption of fenobucarb, endosulfan, and DDT, respectively. The individual effects and interaction of DOC, SDS, and Oxa were evaluated through quadratic regression equations. When the aqueous solution includes 50 mg L-1 DOC, 3.75 CMC SDS, and 0.1 M Oxa, the maximum desorption concentrations of fenobucarb, endosulfan, and DDT were 96, 80, and 75 µg L-1, respectively. The lowest concentration of SDS, DOC, and Oxa caused the minimum desorption. This point at conditions of concern for flooding water is high content of organic compounds causing potentially high contamination by desorption, and the remarkably lower desorption at organic matter-free conditions. The suspended organic matter is one of the common characteristics of flooding and irrigation water in rice fields, and surfactants from pollution increase the problem with desorption of legacy pesticides in the rice fields.

Screening of inorganic and organic contaminants in floodwater in paddy fields of Hue and Thanh Hoa in Vietnam.

In the rainy season, rice growing areas in Vietnam often become flooded by up to 1.5 m water. The floodwater brings contaminants from cultivated areas, farms and villages to the rice fields resulting in widespread contamination. In 2012 and 2013, the inorganic and organic contaminants in floodwater was investigated in Thanh Hoa and Hue. Water samples were taken at 16 locations in canals, paddy fields and rivers before and during the flood. In total, 940 organic micro-pollutants in the water samples were determined simultaneously by GC-MS method with automatic identification and quantification system (AIQS), while ICP-MS was used for determination of ten trace elements in the samples. The concentrations of 277 organic micro-pollutants and ten elements (As, Cu, Cd, Cr, Co, Pb, Zn, Fe, Mn, Al) ranged from 0.01 to 7.6 µg L-1 and 0.1 to 3170 µg L-1, respectively, in the floodwater. Contaminants originated from industrial sources (e.g. PAH) were detected at low concentrations, ranged from 0.01 to 0.18 µg L-1, while concentrations of pollutants originated from domestic sources (e.g. sterols, pharmaceuticals and personal care products and pesticides) were ranged from 0.01 to 2.12 µg L-1. Isoprocarb had the highest detection frequency of 90%, followed by isoprothiolane (88%) and fenobucarb (71%). The results indicated that contaminants in floodwater come from untreated wastewater from villages, and the agricultural activities are the major sources of increased pesticides resuspended in the floodwater in this study.

Screening of 1300 organic micro-pollutants in groundwater from Beijing and Tianjin, North China.

Groundwater contamination in China has become a growing public concern because of the country's rapid economic development and dramatically increasing fresh water demand. However, there is little information available on groundwater quality, particularly with respect to trace organic micro-pollutants contamination. This study was undertaken to investigate the occurrence of 1300 pollutants at 27 groundwater sites in Beijing and Tianjin, North China. Seventy-eight chemicals (6% of the targeted compounds) were detected in at least one sampling point; observed chemicals included polycyclic aromatic hydrocarbons (PAHs), pesticides, plasticizers, antioxidants, pharmaceuticals and other emerging compounds. Chemicals with a frequency of detection over 70% were 2-ethyl-1-hexanol (median concentration 152 ng L-1), benzyl alcohol (582 ng L-1), 2-phenoxy-ethanol (129 ng L-1), acetophenone (74 ng L-1), pentamethylbenzene (51 ng L-1), nitrobenzene (40 ng L-1) and dimethyl phthalate (64 ng L-1). Pesticides with concentrations exceeding the EU maximum residual limits (MRL) of 0.1 µg L-1 were 1,4-dichlorobenzene, oxadixyl, diflubenzuron, carbendazim, diuron, and the E and Z isomers of dimethomorph. Naphthalene and its 7 alkylated derivatives were widely observed at maximum concentration up to 30 µg L-1, which, although high, is still below the Australian drinking water guidelines of 70 µg L-1. The risk assessment indicated there is no human health risk through the oral consumption from most wells, although there were four wells in which total seven compounds were found at the concentrations with a potential adverse health effects. This work provides a wide reconnaissance on broad spectrum of organic micro-contaminants in groundwater in North China.

Groundwater screening for 940 organic micro-pollutants in Hanoi and Ho Chi Minh City, Vietnam.

Groundwater is the main source of drinking water for more than half of the residents of Hanoi (HN). It also provides about one third of the total water demand for residents of Ho Chi Minh City (HCM). However, due to rapid urbanization and frequent discharges of untreated urban wastewater to surface water, freshwater is widely contaminated by man-made chemicals, which may result in groundwater pollution. As part of an ongoing campaign to collect baseline information on the occurrence of organic micro-pollutants (OMPs) in the aquatic environment in Vietnam, 43 water samples were collected from 26 groundwater wells in HN (22) and HCM (4) in September 2013 and August 2014. Samples were analyzed by gas chromatography-mass spectrometry (GC-MS) and the resulting chromatograms were screened for 940 OMPs by an automated identification and quantification system (AIQS) within a GC-MS database. A total of 74 compounds were detected, with between 4 and 43 (median 18) compounds found at each site. Overall, contamination levels were low, with over 89 % of the detected concentrations that were less than 0.5 µg L(-1). Results suggest that most of the sampled aquifers have been impacted by non-point source pollution. Most of the contaminants detected are either currently not regulated in drinking water or are present at low levels. A health risk assessment for detected contaminants implied that there were no risks to humans. Since this study was based on a limited number of samples, especially in HCM, further, more detailed studies on the occurrence of OMPs in groundwater in HCM and a full risk assessment of detected contaminants should be prioritized.

Monitoring of 1300 organic micro-pollutants in surface waters from Tianjin, North China.

In spite of the quantities and species of chemicals dramatically increased with rapid economic growth in China in the last decade, the focus of environmental research was mainly on limited number of priority pollutants. Therefore, to elucidate environmental pollution by organic micro-pollutants, this work was conducted as the first systematic survey on the occurrence of 1300 substances in 20 surface water samples of Tianjin, North China, selected as a representative area of China. The results showed the presence of 227 chemicals. The most relevant compounds in terms of frequency of detection and median concentration were bis(2-ethylhexyl) phthalate (100%; 0.26µgL(-1)), siduron (100%; 0.20µgL(-1)), lidocaine (100%; 96ngL(-1)), antipyrine (100%; 76ngL(-1)), caffeine (95%; 0.28µgL(-1)), cotinine (95%; 0.20µgL(-1)), phenanthrene (95%; 0.17µgL(-1)), metformin (90%; 0.61µgL(-1)), diethyl phthalate (90%; 0.19µgL(-1)), quinoxaline-2-carboxylic acid (90%; 0.14µgL(-1)), 2-(methylthio)-benzothiazole (85%; 0.11µgL(-1)) and anthraquinone (85%; 54ngL(-1)). Cluster analysis discriminated three highly polluted sites from others based on data similarity. Principle component analysis identified four factors, corresponding to industrial wastewater, domestic discharge, tire production and atmospheric deposition, accounting for 78% of the total variance in the water monitoring data set. This work provides a wide reconnaissance on broad spectrum of organic micro-contaminants in surface waters in China, which indicates that the aquatic environment in China has been polluted by a large number of chemicals.

Occurrence of perfluoroalkyl acids in environmental waters in Vietnam.

This is the first nationwide study of perfluoroalkyl acids (PFAAs) in environmental waters in Vietnam. Twenty-eight river water and 22 groundwater samples collected in four major cities and 14 river water samples from the Red River were screened to investigate the occurrence and sources of 16 PFAAs. Perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA), and perfluorononanoic acid (PFNA) were the most prevalent of 11 detected PFAAs with maximum concentrations in urban river water of 5.3, 18 and 0.93ngL(-1), respectively, and in groundwater of 8.2, 4.5 and 0.45ngL(-1), respectively. PFAAs in the Red River water were detected at low levels. PFAA concentrations in river water were higher in the rainy season than in the dry season, possibly due to storm water runoff, a common phenomenon in Southeast Asian countries. The highest concentrations of PFAAs in river water were observed in samples from highly populated and industrialized areas, perhaps sourced from sewage. The PFAA concentrations observed were similar to those in other Southeast Asian countries, but lower than in developed nations. From the composition profiles of PFAAs, industrial products containing PFAAs imported from China and Japan might be one of the major sources of PFAAs in the Vietnamese aquatic environment. According to the health-based values and advisory issued by the United States Environmental Protection Agency (USEPA), the concentrations of detected PFAAs in this study do not pose an immediate health risk to humans and aquatic organisms.

Screening and analysis of 940 organic micro-pollutants in river sediments in Vietnam using an automated identification and quantification database system for GC-MS.

In order to obtain a detailed picture of pollution by organic micro-pollutants in Vietnamese rivers, 940 semi-volatile organic compounds in river sediments collected from four major cities were examined by a comprehensive gas chromatography-mass spectrometry-database. The number of detected chemicals at each site ranged from 49 to 158 (median 96 out of 940) with 185 analytes detected at least once in the survey. The substances detected with high frequency (over 80%) and high concentrations were n-alkanes, phthalates, sterols and PAHs. For most substances, sediments from metropolitan areas (Hanoi and Ho Chi Minh City) were more heavily contaminated than those in rural and suburban areas. Sterols were observed in nearly 100% of sediments at extremely high concentrations, suggesting that the studied rivers were contaminated by sewage. Pyrethroids (permethrin-1 and -2) were the most dominant insecticides found in inner canals of Hanoi and Ho Chi Minh City. Deltamethrin was only detected at a site in Hanoi at an elevated concentration. This reflects that pyrethroids are used for the protection of private and public health rather than for agriculture. p,p'-DDE and p,p'-DDD were the dominant members of the DDT family of chemicals detected, indicating no recent inputs of DDTs in the study areas. PCBs residues were lower than those in other Asian countries, which suggest historically much lower use of PCBs in Vietnam. PAHs pollution in urban areas is caused by the runoff of petroleum products and vehicle exhaust gases, whereas in rural and suburban areas, the combustion of fossil fuels and biomass is major sources of PAHs. Overall, the study confirmed that rivers in Vietnam were heavily polluted mainly by domestic wastewater.

Target and screening analysis of 940 micro-pollutants in sediments in Tokyo Bay, Japan.

Urban societies are using an increasingly diverse array of chemicals, many of which ultimately end up accumulating in urban harbors, where they can act as contaminants alone or as part of a mixture. In attempt to grasp a more complete picture of anthropogenic chemicals in an urban harbor, we analyzed 940 organic chemicals in sediments in Tokyo Bay, one of the most densely populated and modernized areas in the world. For the chemical analysis, we used targeted analytical methods using a GC-MS-MS and a GC-MS-SIM, and a screening analysis using an automated identification and quantification system with a GC-MS database. We detected 195 organic chemicals in the sediments; the sum of concentrations of compounds detected varied from 6095 to 39140µgkg(-1)dry wt. Since their concentrations increased with proximity to the innermost part of the bay, their sources seem to be mainly sewage treatment plants (STPs) and rivers flowing to this area. Additional confirmation comes from the nature of the identified pollutants, which are characteristic of chemicals used in households as well as fecal matter, business activities and urban run-off. From these results, it was confirmed that sediments in Tokyo Bay are still polluted with a wide range of chemicals, particularly domestic chemicals, despite nearly 100% of wastewater from household and business activities being treated by STPs.