磷细菌筛选及其对苗期玉米生长的影响

从潮土、水稻土、砂姜黑土、石灰土上植物根际土壤和根中分离了86株磷细菌,通过NBRIP液体摇瓶培养3 d,培养液水溶磷质量浓度为4.2～387.3 mg.L^-1,水溶磷质量浓度与培养液pH呈显著负相关（r^2=0.621 6）。筛选出3株磷细菌进行玉米盆栽试验,结果表明,1株磷细菌处理的玉米干物质量和吸磷量与对照（处理4）相比无显著差异,2株磷细菌处理的玉米干物质量和吸磷量与对照相比有明显增加,干物质量增加了19.6%～37.5%,吸磷量增加了22.7%～40.2%,其中编号为HCW115解磷菌株的效果相当于施用无机磷（P）10 mg.kg^-1处理。     

Using hydrochemical signatures to characterize the long-period evolution of groundwater information in the Dagu River Basin,China

• The long-period groundwater evolution was identified by hydrochemical signatures. • The dominant processes in the groundwater evolution were verified. • Groundwater quality in the coastal areas was susceptible to deterioration due to SI. • Groundwater contamination arose from fertilizer, livestock manure & domestic sewage. The evolution of hydrochemical compositions influenced by long-period interactions between groundwater and the geo-environment is a fundamental issue for exploring groundwater quality and vulnerability. This study systematically investigated the hydrochemical processes and anthropogenic interference occurring in the river basin by bivariate plots, Gibbs diagrams, saturation index, and the major ions ratios. Apparent changes in groundwater hydrochemistry have been observed in the study area, illustrating the origins of major ions are affected by various internal and external factors. Results highlighted that TDS varied from freshwater to brackish water, ranging between 187.90 and 2294.81 mg/L. Ca²⁺ and HCO₃⁻ are the dominant ions in the studied samples. The results gained by Gibbs diagrams, bivariate plots, saturation index, and the major ions ratios demonstrated that minerals dissolution/precipitation, cation exchange, and human inputs play crucial roles in the unconfined aquifers. Moreover, the overuse of nitrogen fertilizer, livestock manure, and industrial/domestic sewage led to nitrate and nitrite contamination and brought significant challenges to the surrounding hydrogeo-environment. The present study could make an unambiguous identification of natural processes and anthropogenic interventions influencing groundwater hydrochemistry’s long-period evolution and create a preliminary strategy for groundwater resources management.     

Characteristics of plankton Hg bioaccumulations based on a global data set and the implications for aquatic systems with aggravating nutrient imbalance

• Hg bioaccumulation by phytoplankton varies among aquatic ecosystems. • Active Hg uptake may exist for the phytoplankton in aquatic ecosystems. • Impacts of nutrient imbalance on food chain Hg transfer should be addressed. The bioaccumulation of mercury (Hg) in aquatic ecosystem poses a potential health risk to human being and aquatic organism. Bioaccumulations by plankton represent a crucial process of Hg transfer from water to aquatic food chain. However, the current understanding of major factors affecting Hg accumulation by plankton is inadequate. In this study, a data set of 89 aquatic ecosystems worldwide, including inland water, nearshore water and open sea, was established. Key factors influencing plankton Hg bioaccumulation (i.e., plankton species, cell sizes and biomasses) were discussed. The results indicated that total Hg (THg) and methylmercury (MeHg) concentrations in plankton in inland waters were significantly higher than those in nearshore waters and open seas. Bioaccumulation factors for the logarithm of THg and MeHg of phytoplankton were 2.4–6.0 and 2.6–6.7 L/kg, respectively, in all aquatic ecosystems. They could be further biomagnified by a factor of 2.1–15.1 and 5.3–28.2 from phytoplankton to zooplankton. Higher MeHg concentrations were observed with the increases of cell size for both phyto- and zooplankton. A contrasting trend was observed between the plankton biomasses and BAF_MeHg, with a positive relationship for zooplankton and a negative relationship for phytoplankton. Plankton physiologic traits impose constraints on the rates of nutrients and contaminants obtaining process from water. Nowadays, many aquatic ecosystems are facing rapid shifts in nutrient compositions. We suggested that these potential influences on the growth and composition of plankton should be incorporated in future aquatic Hg modeling and ecological risk assessments.     

Modeling porosity reductions caused by mineral fouling in continuous-wall permeable reactive barriers

A study was conducted to assess key factors to include when modeling porosity reductions caused by mineral fouling in permeable reactive barriers (PRBs) containing granular zero valent iron. The public domain codes MODFLOW and RT3D were used and a geochemical algorithm was developed for RT3D to simulate geochemical reactions occurring in PRBs. Results of simulations conducted with the model show that the largest porosity reductions occur between the entrance and mid-plane of the PRB as a result of precipitation of carbonate minerals and that smaller porosity reductions occur between the mid-plane and exit face due to precipitation of ferrous hydroxide. These findings are consistent with field and laboratory observations, as well as modeling predictions made by others. Parametric studies were conducted to identify the most important variables to include in a model evaluating porosity reduction. These studies showed that three minerals (CaCO3, FeCO3, and Fe(OH)2 (am)) account for more than 99% of the porosity reductions that were predicted. The porosity reduction is sensitive to influent concentrations of HCO3-, Ca2+, CO3(2-), and dissolved oxygen, the anaerobic iron corrosion rate, and the rates of CaCO3 and FeCO3 formation. The predictions also show that porosity reductions in PRBs can be spatially variable and mineral forming ions penetrate deeper into the PRB as a result of flow heterogeneities, which reflects the balance between the rate of mass transport and geochemical reaction rates. Level of aquifer heterogeneity and the contrast in hydraulic conductivity between the aquifer and PRB are the most important hydraulic variables affecting porosity reduction. Spatial continuity of aquifer hydraulic conductivity is less significant.     

琼脂碳源生物反硝化去除水源水中硝酸盐

针对受硝酸盐污染的水源水,以琼脂为反硝化细菌的碳源和微生物载体,通过生物反硝化作用脱除水源水中的硝酸盐,并利用曝气生物滤池(BAF)去除琼脂反应器出水中残留的少量CODMn和NO2--N等污染物。实验结果表明,水源水自然接种的条件下,可以顺利启动琼脂反应器;在温度为25℃左右,琼脂反应器在进水NO3--N约25 mg/L、水力停留时间1.5 h时,能获得70%的硝酸盐氮去除率;曝气生物滤池在水力停留时间0.5 h、气水比2.8时,可控制最终出水的CODMn和NO2--N分别在5.0 mg/L和0.10 mg/L以下;琼脂反应器的脱氮效果与温度、进水NO3--N浓度及水力停留时间等有关。研究指出,琼脂反应器与曝气生物滤池构成的组合系统能较好地脱除水源水中的硝酸盐并且能控制最终出水水质,不会导致二次污染,从而获得合格的饮用水源水。     

Decomposition of perfluorocarboxylic acids (PFCAs) by heterogeneous photocatalysis in acidic aqueous medium

Decomposition of perfluorocarboxylic acids (PFCAs) is of prime importance since they are recognized as persistent organic pollutants and are widespread in the environment. PFCAs with longer carbon chain length are particularly of interest because of their noted recalcitrance, toxicity, and bioaccumulation. Here in this study, we demonstrate efficient decomposition of three important PFCAs such as perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA) and perfluorodecanoic acid (PFDA) by heterogeneous photocatalysis with TiO₂ as a photocatalyst in acidic aqueous solutions. The PFCAs were decomposed into shorter carbon chain length PFCAs and fluoride ions. Photoholes of excited TiO₂ generated upon UV-irradiation are found to be the oxidation sites for PFCAs. Therefore, creation and sustenance of these photoholes in the acidic aqueous medium has enhanced the decomposition of PFCAs. Heterogeneous photocatalytic treatment achieved more than 99% decomposition and 38% complete mineralization of PFOA in 7 h. The decomposition of other PFCAs was as high as 99% with a defluorination efficiency of 38% for PFDA and 54% for PFNA. The presence of perchloric acid was found to enhance the decomposition by facilitating the ionization of PFCAs. The oxygen present in the medium served both as an oxidant and an electron acceptor. The mechanistic details of PFCA decomposition and their corresponding mineralization are elaborated.     

荧光化学传感器的制备及其在环境分析监测中的应用

随着荧光分析技术和传感技术的发展,荧光化学传感器已经成为一种重要的连续分析测量装置.它具有很高的选择性和灵敏度,可以实现对pH、溶解氧、含氮化合物、有毒害重金属离子、有机污染物进行实时和在线测定,因此在环境分析监测方面具有广泛的应用前景.简要介绍了荧光化学传感器的原理、制备及分类,综述了近年来荧光化学传感器的发展及其在环境分析监测中的最新研究成果,并探讨了荧光化学传感器在环境分析监测领域的应用前景和发展方向.     

Mn2O3/γ-Al2O3在超临界水氧化中催化活性的研究

采用浸渍法制备了Mn2O3/γ-Al2O3催化剂,在超临界水中催化氧化降解1,5-萘二磺酸,探索了催化剂Mn2O3活性组分负载量、催化剂空速和反应溶液pH对Mn2O3/γ-Al2O3催化剂活性的影响。结果表明：Mn2O3/γ-Al2O3的催化活性在一定范围内随Mn2O3活性组分负载量的增加而提高;在一定范围内,Mn2O3/γ-Al2O3空速越小,模拟废水的COD去除率越高;Mn2O3/γ-Al2O3催化活性在反应溶液呈酸性情况下比碱性时高。     

Fate of polycyclic aromatic hydrocarbons during vitrification of incinerator ash in a coke bed furnace

Fate of polycyclic aromatic hydrocarbons (PAHs) during the vitrification of fly ash and bottom ash from the municipal waste incinerator in a coke bed furnace was investigated. In this system, both coke and lime were added to enhance the melting reaction. The major PAH sources in this system were ash and coke, which respectively contributed 97% and 3% of PAHs in the input-mass. During vitrification process, low molecular PAHs (LM-PAH, 2-3-ring), median molecular PAHs (MM-PAH, 4-ring) and high molecular PAHs (HM-PAH, 5-7-ring) mass respectively accounted for >99%, >99% and 84% of the output-mass emitted as the stack flue gas; while those discharged from the slag were <1%, <1% and 16%, respectively. The O/I (output-mass/input-mass) ratio of LM-, MM- and HM-PAHs were 0.063, 0.002 and <0.001, respectively. The high distribution in flue gas and O/I ratio of LM-PAHs is reasonable since they are more easily evaporated, hence difficult to be removed by air pollution control devices. On the contrary, the HM-PAHs, having lower vapor pressure, primarily stays mainly in slag. Based on the 21 total PAH content in feeding ash and slag, the reduction efficiency of the coke bed furnace was >99.9%. To minimize the risk of secondary pollution, the efficiency of coke bed furnace should be improved to reduce the PAH emission into ambient air.     

再入飞行力热环境预测与试验技术研究进展

总结了近5年来再入飞行力热环境预测与试验技术的研究进展.针对高速绕流流场引起的宽频声振环境和瞬态热环境,调研了国内外在上述环境的数值模拟预测、等效模拟试验和试验观测方面的最新研究情况和目前仍面临的难点问题.重点介绍了中物院总体所围绕再入飞行力热环境预测与试验方面开展的研究工作和已取得的部分研究成果.提出了后续研究方向和...