Perfluoroalkyl substances (PFAS) in freshwater fish from urban lakes in Hanoi, Vietnam: concentrations, tissue distribution, and implication for risk assessment.

Concentrations and profiles of 17 perfluoroalkyl substances (PFAS) including 13 perfluorocarboxylic acids (PFA) and 4 perfluoroalkyl sulfonates (PFS) were determined in whole blood, muscle, and liver samples of four freshwater fish species in West Lake and Yen So Lake (Hanoi, Vietnam). Concentrations of total 17 PFAS in fish blood samples ranged from 5.2 to 29 (median 16) ng/mL. Total 17 PFAS levels in liver samples (4.5; 2.7-6.6 ng/g wet weight) were significantly higher than in muscle samples (1.0; 0.51-2.6 ng/g wet weight). More than 90% PFAS burdens in our fish samples were attributed to muscle and blood rather than liver, but contributions of individual compounds varied greatly. The most predominant substances were perfluorooctanesulfonate (PFOS) and PFA with chain lengths from C10 to C14 (i.e., PFDA, PFUnDA, PFDoDA, PFTrDA, and PFTeDA). There is no significant difference in PFAS concentrations between the studied species (i.e., bighead carp, common carp, rohu, and tilapia), but common carp showed specific PFAS profiles as compared to other species (e.g., higher proportions of PFOS and long-chain PFA such as PFTrDA, PFTeDA, and PFHxDA). Daily intake doses of PFOS and perfluorooctanoic acid (PFOA) through fish consumption were markedly lower than the US EPA reference dose of 20 ng/kg/day. Weekly intakes of the sum of PFHxS, PFOS, PFOA, and PFNA in our study were still lower than the EFSA tolerable weekly intake of 4.4 ng/kg/week.

Soil and sediment contamination by unsubstituted and methylated polycyclic aromatic hydrocarbons in an informal e-waste recycling area, northern Vietnam: Occurrence, source apportionment, and risk assessment.

Improper processing activities of e-waste are potential sources of polycylic aromatic hydrocarbons (PAHs) and their derivatives, however, information about the environmental occurrence and adverse impacts of these toxic substances is still limited for informal e-waste recycling areas in Vietnam and Southeast Asia. In this study, unsubstituted and methylated PAHs were determined in surface soil and river sediment samples collected from a rural village with informal e-waste recycling activities in northern Vietnam. Total levels of PAHs and MePAHs decreased in the order: workshop soil (median 2900; range 870-42,000 ng g-1) > open burning soil (2400; 840-4200 ng g-1) > paddy field soil (1200; range 530-6700 ng g-1) > river sediment samples (750; 370-2500 ng g-1). About 60% of the soil samples examined in this study were heavily contaminated with PAHs. Fingerprint profiles of PAHs and MePAHs in the soil and sediment samples indicated that these pollutants were mainly released from pyrogenic sources rather than petrogenic sources. The emissions of PAHs and MePAHs in this area were probably attributed to uncontrolled burning of e-waste and agricultural by-products, domestic coal and biomass combustion, and traffic activities. Carcinogenicity and mutagenicity of PAHs in the e-waste workshop soils were significantly higher than those of the field soils; however, the incremental lifetime cancer risk of PAH-contaminated soils in this study ranged from 5.5 × 10-9 to 4.6 × 10-6, implying acceptable levels of human health risk. Meanwhile, concentrations of some compounds such as phenanthrene, anthracene, fluoranthene, benz[a]anthracene, and benzo[a]pyrene in several soil samples exceeded the maximum permissible concentrations, indicating the risk of ecotoxicological effects.

Facile design of an ultra-thin broadband metamaterial absorber for C-band applications.

We report a facile design of an ultra-thin broadband metamaterial absorber (MA) for C-band applications by utilizing a single layer of a metal-dielectric-metal structure of FR-4 substrate. The absorption performances are characterized using a numerical method. The proposed MA exhibits the broadband absorption response over the entire C-band spectrum range from 4.0 GHz to 8.0 GHz with absorptivity above 90% and the high absorptivity is remained over 80% for a large incident angle up to 40° under both transverse electric (TE) and transverse magnetic (TM) polarizations over the band. The origin of absorption mechanism is explained by the electric and surface current distributions, which is also supported by the retrieved constitutive electromagnetic parameters, significantly affected by magnetic resonance. In addition, compared with the previous reports, the proposed MA presents a greater practical feasibility in term of low-profile and wide incident angle insensitivity, suggesting that the proposed absorber is a promising candidate for C-band applications.

Graphene-platinum nanohybrid as a robust and low-cost counter electrode for dye-sensitized solar cells.

Dry plasma reduction (DPR) is an excellent approach for easily, continuously, uniformly and stably hybridizing platinum nanoparticles (Pt-NPs) on a graphene-coated layer under atmospheric pressure without any toxic chemicals and at a low temperature. The Pt-NPs with a size of 0.5-4 nm and mostly 2 nm were stably and uniformly hybridized on the surface of reduced graphene oxide (RGO) after co-reduction of Pt precursor ions and GO to Pt atoms and RGO, respectively. XPS analysis also revealed a repair of structural damage on the basal plane of the graphene as well as chemical bonding between Pt-NPs and RGO after DPR. Thus, the Pt-NPs/RGO nanohybrids applied to the counter electrode of dye-sensitized solar cells (DSCs) exhibited robust stability as well as ultrahigh electrochemical catalytic activity and conductivity using less than 1% of the Pt exploited for the Pt-sputtered counter electrodes. Thus, the Pt-NPs/RGO nanohybrid fabricated by DPR could be an excellent material for a robust and low-cost counter electrode for DSCs.

Effects of reduced chemical vapor deposition environment on growth and optical characteristics of TiO2 nanobelts.

TiO2-delta nanobelts were self-catalytically grown at 510 degrees C on bare Si (100) substrates using metallorganic chemical vapor deposition. The nanobelt formation was critically affected by the partial pressure of oxygen. The nanobelts were grown when supplying only Ar or a mixed gas of Ar (90%) and H2 (10%), while thin films were formed with an O2 gas flow of more than 50 cm3 min(-1). The nanobelts consisted of approximately 20-30 nm size rutile-dominant nanocrystallites. A vapor-solid growth mechanism excluding a liquid phase appeared to control the nanobelt formation. The grown TiO2-delta nanobelts showed a strong photoluminescence (PL) spectra peak at approximately 550 nm due to oxygen vacancies. The nanobelt surface possessed significant amount of oxygen vacancies contributing PL and actively reacting with the environment, indicating promise for photocatalytic and gas sensor applications in a visible light regime.