Distribution and chemical speciation of arsenic in different sized atmospheric particulate matters

The distribution and chemical speciation of arsenic (As) in different sized atmospheric particulate matters (PMs), including total suspended particles (TSP), PM₁₀, and PM_2.5, collected from Baoding, China were analyzed. The average total mass concentrations of As in TSP, PM₁₀, and PM_2.5 were 31.5, 35.3, and 54.1 µg/g, respectively, with an order of PM_2.5 >PM ₁₀ > TSP, revealing that As is prone to accumulate on fine particles. Due to the divergent toxicities of different As species, speciation analysis of As in PMs is further conducted. Most of previous studies mainly focused on inorganic arsenite (iAs^III), inorganic arsenate (iAs^V), monomethylarsonate (MMA), and dimethylarsinate (DMA) in PMs, while the identification and sensitive quantification of trimethylarsine oxide (TMAO) were rarely reported. In this study, a high-performance liquid chromatography coupled to inductively coupled plasma mass spectrometry system was optimized for As speciation including TMAO in PMs. An anion exchange column was used to separate MMA, DMA and iAs^V, while a cation exchange column to separate TMAO and iAs^III. Results showed that iAs^V was the dominate component in all the samples, corresponding to a portion of 79.2% ± 9.3% of the total extractable species, while iAs^III, TMAO and DMA made up the remaining 21%. Our study demonstrated that iAs^III accounted for about 14.4% ± 11.4% of the total extracted species, with an average concentration of 1.7 ± 1.6 ng/m³. It is worth noting that TMAO was widely present in the samples (84 out of 97 samples), which supported the assumption that TMAO was ubiquitous in atmospheric particles.     

Programmed cell death induced by modified clay in controlling Prorocentrum donghaiense bloom

Modified clay (MC), an effective material used for the emergency elimination of algal blooms, can rapidly reduce the biomass of harmful algal blooms (HABs) via flocculation. After that, MC can still control bloom population through indirect effects such as oxidative stress, which was initially proposed to be related to programmed cell death (PCD) at molecular level. To further study the MC induced cell death in residual bloom organisms, especially identifying PCD process, we studied the physiological state of the residual Prorocentrum donghaiense. The experimental results showed that flocculation changed the physiological state of the residual cells, as evidenced by growth inhibition and increased reactive oxygen species production. Moreover, this research provides biochemical and ultrastructural evidence showing that MC induces PCD in P. donghaiense. Nuclear changes were observed, and increased caspase-like activity, externalization of phosphatidylserine and DNA fragmentation were detected in MC-treated groups and quantified. And the mitochondrial apoptosis pathway was activated in both MC-treated groups. Besides, the features of MC-induced PCD in a unicellular organism were summarized and its concentration dependent manner was proved. All our preliminary results elucidate the mechanism through which MC can further control HABs by inducing PCD and suggest a promising application of PCD in bloom control.     

Enhanced the photoelectrochemical performance of Bi2XO6 (X = W, Mo) for detecting hexavalent chromium by modification of CuS

In this work, Bi₂XO₆ (X = W, Mo) are synthesized at different temperatures. The results of tests find the optimal temperatures of Bi₂WO₆ and Bi₂MoO₆ are 180 and 160°C (BW-180, BM-160). Then, BW-180 and BM-160 are further compounded with different contents of CuS. The results of photoelectrochemical (PEC) tests show that CuS can improve the PEC performance of semiconductor materials, and it has better performance when CuS mass fraction is 5%. These maybe the photoelectron potentials generated by CuS/Bi₂XO₆ (X = Mo, W) heterojunction reduce the combination of photogenerated electrons and holes. When the PEC sensor based on 5%-CuS/BW-180 detects Cr(VI), it has a linear range of 1–80 μmol/L with detection limit of 0.95 μmol/L, while the PEC sensor based on 5%-CuS/BM-160 detects Cr(VI) has a linear range of 0.5–230 μmol/L and a detection limit of 0.12 μmol/L. Thus, 5%-CuS/Bi₂XO₆ has potential application in hexavalent chromium detection.     

上海市屋面雨水回用处理技术研究

在分析上海市屋面雨水水质的基础上,研究了沉淀和过滤技术对屋面雨水的回用处理效果。结果表明,经过沉淀、过滤处理后,屋面雨水满足城市生活杂用水和景观用水的水质标准。     

Effects of soil nematodes communities on litter decomposition in urban forest of Dalian北大核心CSCD

In order to further expound the effect of soil nematodes on litter decomposition in urban forest, this study investigated the responses of soil nematodes communities to litter decomposition by litterbags technology at different mesh sizes in Dalian National Forest Park. Soil nematodes community composition, decomposition rate of litter and nutrient release were also analyzed. It found a total of 4 418 nematodes from 39 genera. Higher relative density of soil nematodes was found in the bags with 0.1 mm mesh size (1.55 individuals and 7.34 orders per g of dry litter) compared to the bags with 0.02 mm mesh size (0.21 individuals and 0.49 orders per g of dry litter). There were very few soil nematodes in the 0.02 mm litter bags. Thus we regarded that soil nematodes only affected the 0.1 mm litter bags. The mass loss rates as well as C and P release rates was higher in litter bags with 0.1 mm mesh size than in those with 0.02 mm mesh size, indicating a significant influence of soil nematodes on mass loss and nutrient release. The contribution of soil nematodes to the litter mass loss was about 24%. The effect of soil nematodes on the nutrient release rates differed among elements. The soil nematodes had a bigger influence on the release rate of N than that of other elements, whereas the influence on K release rate was the lowest. The results showed that soil nematodes communities has a significant effect on the litter decomposition and nutrient release of the forest litter in Dalian city, especially promoting the mass loss rates and N release rates.     

Contents and sources of polycyclic aromatic hydrocarbons and organochlorine pesticides in vegetable soils of Guangzhou, China

We investigated contents, distribution and possible sources of PAHs and organochlorine pesticides (Ops) in 43 surface and subsurface soils around the urban Guangzhou where variable kinds of vegetables are grown. The results indicate that the contents of PAHs (16 US EPA priority PAHs) range from 42 to 3077 microg/kg and the pollution extent is classified as a moderate level in comparison with other investigations and soil quality standards. The ratios of methylphenanthrenes to phenanthrene(MP/P), anthracene to anthracene plus phenanthrene (An/178), benz[a]anthracene to benz[a]anthracene plus chrysene (BaA/228), indeno[1,2,3-cd]pyrene to indeno[1,2,3-cd]pyrene plus benzo[ghi]perylene (In/In+BP) suggest that the sources of PAHs in the soil samples are mixed with a dominant contribution from petroleum and combustion of fossil fuel. The correlation analysis shows that the PAHs contents are significantly related to total organic carbon contents (TOC) (R2=0.75) and black carbon contents (BC) (R2=0.62) in the soil samples. Dichlorodiphenyltrichloroethane and metabolites (DDTs) and hexachlorocyclohexanes and metabolites (HCHs) account largely for the contaminants of OPs. The concentrations of DDTs range from 3.58 to 831 microg/kg and the ratios for DDT/(DDD+DDE) are higher than 2 in some soil samples, suggesting that DDT contamination still exists and may be caused by its persistence in soils and/or impurity in the pesticide dicofol. The concentrations of HCHs are 0.19-42.3 microg/kg.     

Kinetic studies of the reaction of hydroxyl radicals with trichloroethylene and tetrachloroethylene

Rate coefficients are reported for the gas-phase reaction of the hydroxyl radical (OH) with C2HCl3 (k(1)) and C2Cl4 (k2) over an extended temperature range at 740+/-10 Torr in a He bath gas. These absolute rate measurements were accomplished using a laser photolysis/laser-induced fluorescence (LP/LIF) technique under slow flow conditions. The simple Arrhenius equation adequately describes the low temperature data for k1 (<650 K) and the entire data set for k2 and is given by (in units of cm3 molecule(-1) s(-1)): k1(291 - 650 K) = (9.73+/-1.15) x 10(-13) exp (158.7+/-44.0)/T, k2(293 - 720 K ) = (1.53+/-0.14) x 10(-12) exp (-688.2+/-67.5)/T. Error limits are 2sigma values. The room temperature values for k1 and k2 are within +/-2sigma of previous data using different techniques. The Arrhenius activation energies for k1 and k2 are a factor of 2-3 lower than previously reported values. The experimental measurements for both k1 and k2 in conjunction with transition state and variation transition state theory calculations infer an OH addition mechanism. The lack of a measurable kinetic isotope effect for k1 is consistent with this mechanism. Insight into the subsequent reactions of the chemically activated intermediate are presented in the form of potential energy diagrams derived from ab initio calculations.     

Evidence for the contribution of methane in the formation of aromatics and soot in fuel-rich pre-mixed combustion

Experimental results from an isothermal laminar flow reactor at atmospheric pressure are presented on the chemical composition in the post-oxidative region of two sooting fuel-rich pre-mixed mixtures diluted in nitrogen. A base case composed of n-heptane and O2 in N2 at 1425 K with a C/O of 2.85 was perturbed by substituting 10% of the carbon in n-heptane with carbon as CH4. While these changes would intuitively reduce aromatics and soot formation by increasing H2 and decreasing C2H2 concentrations, we observe the opposite. The concentrations of individual aromatic species are observed to actually increase by up to 50% and the soot yield increases by 80%.     

Fabrication of PVA/GO Nanofiber Films by Electrospinning: Application for the Adsorption of Cu2+ and Organic Dyes

Journal of Polymers and the Environment - In recent years, the treatment of water pollution has been a challenging and far-reaching topic. In order to improve the adsorption performance of...