固定化菌藻系统对污水处理厂出水的深度处理

将海藻酸钠固定化活性污泥和小球藻制成颗粒小球,以自制的流化床反应器对重庆市某污水处理厂出水进行深度处理,探讨了系统对氨氮、TP、COD的去除效果,实验结果表明:在HRT=12 h,溶解氧浓度为3.0 mg/L左右,pH值为6.2至8.0之间,环境室温条件下,系统对氨氮、TP、COD均有较好的去除效果,系统稳定运行后对氨氮、TP、COD去除率基本维持在60%、60%和30%以上,出水氨氮、TP、COD浓度基本维持在8、0.5和40 mg/L以下,出水浓度达到了《城镇污水处理厂污染物排放标准》(GB 18918-2002)的一级A标准。这项研究显示固定化菌藻胶球系统在污水处理厂出水的深度处理中具有潜在的应用前景。     

汞矿区周边农田土壤微生物群落结构特征及其环境驱动因子

为探究汞矿区周边农田土壤微生物群落结构特征及其与环境驱动因子关系,以铜仁汞（Hg）矿区周边（碧江区坝黄镇、石阡县花桥镇、江口县凯德镇和碧江区川硐镇,分别用BJ、SQ、JK和TR表示）农田土壤为研究对象,分析了土壤理化性质、Hg污染状况、酶活性以及微生物群落结构特征.采用冗余分析（RDA）和相关性网络分析了土壤微生物群落结构与环境因子互作关系.结果表明,研究区土壤存在一定程度的Hg污染,其中,JK和TR属于轻度污染,SQ和BJ属于偏中度污染;TR存在中等潜在生态风险,BJ和JK存在强潜在生态风险,SQ存在很强潜在生态风险.研究区土壤的主要细菌优势菌群包括：变形菌门（Proteobacteria）、放线菌门（Actinobacteria）、酸杆菌门（Acidobacteria）和绿弯菌门（Chloroflexi）;主要真菌优势菌群包括：子囊菌门（Ascomycota）、担子菌门（Basidiomycota）和被孢霉门（Mortierellomycota）.RDA分析表明,pH、蔗糖酶（SC）和过氧化氢酶（CAT）活性是土壤细菌群落结构组成的主要环境因子,pH、碱解氮（AN）、速效钾（AK）、HCl-Hg、酸性磷酸酶（ACP）和脲酶（URE）活性是土壤真菌群落结构组成的主要环境因子.相关性网络分析表明,pH、AP、HCl-Hg、SC、ACP和CAT是影响土壤Proteobacteria、Acidobacteria、Actinobacteria、Chloroflexi、厚壁菌门（Firmicutes）、棒状杆菌门（Rokubacteria）和浮霉菌门（Planctomycetes）等细菌群落结构的主要环境因子;而AK、pH、TN、AP、AN、ACP、URE和SC活性是影响土壤Ascomycota、Basidiomycota、Mortierellomycota、球囊菌门（Glomeromycota）、壶菌门（Chytridiomycota）、红藻门（Rozellomycota）、梳霉门（Kickxellomycota）和Mucoromycota （毛霉门）等真菌群落结构的主要环境因子.     

洪泽湖西部湖滨水质污染特征分析

根据2010年洪泽湖西部湖滨的常规监测资料,对洪泽湖西部湖滨主要污染物因子的时空分布特征及其水质污染特征进行了初步研究。结果表明,洪泽湖西部湖滨总体水质为Ⅴ类,处于重污染水平,TP、TN是影响洪泽湖西部湖滨水质的主要污染物。氨氮、TN、COD Mn在时空分布上均无显著差异,TP、COD有显著差异,枯水期时空分异性大于平水期、丰水期。各河口Chl-a浓度普遍高于敞水区。虽然湖水中TP、TN的浓度已达到较高的水平,但没有达到全面富营养化的程度。     

总有机碳分析仪测定水中的游离二氧化碳

利用总有机碳分析仪、结合酸化吹气装置对水样中的游离二氧化碳的测定条件进行试验。结果表明水浴温度80℃,流量150 ml/min通氮气30 min为水样释放游离二氧化碳的最佳条件。总有机碳分析测定水中游离二氧化碳含量方法的建立为水质分析提供了新的方法参考。     

Historical trends in the anthropogenic heavy metal levels in the tidal flat sediments of Lianyungang, China

The sedimentation of metals can preserve the historical record of contaminant input from local and regional sources and provide information on the historical changes in regional water and sediment quality. We report the ²¹⁰Pb activities and the heavy metal (Cd, Cr, Cu, Mn, Pb and Zn) depth profiles from sediment cores retrieved in 2010. The mean sedimentation rates of 0.85-1.5 cm/yr are determined by ²¹⁰Pb dating. The sediments in the tidal flat have recorded heavy metal deposition and thus allow the establishment of a connection between the temporal evolution of the heavy metal pollution and the historical changes in the economic development of Lianyungang. The enrichment factors (EF) are calculated to estimate the level of contamination stored in these sediments. The results show that in the studied sites, Cr and Cu display low EF values and are mainly from lithogenic origin. For the other studied trace metals, a great variability in the sedimentary record is observed. Significant anthropogenic enrichment over the last 50 years is revealed at the tidal flat that receives fluvial inputs. Zinc is the element with the highest EF values, followed by the order of Pb > Cd > Mn > Cu and Cr. The temporal variations of the heavy metals peak during the late 1980s to the early 2000s and show a decreasing trend afterward. The pollution intensity of the tidal flat is determined by using EF and the geo-accumulation index (I_geo), which show that, based on the I_geo scale, the tidal flat of Haizhou Bay is unpolluted to moderately polluted.     

重金属污染河道底泥稳定化固化修复工程技术研究

介绍了某市排污渠重金属污染治理工程中对重金属污染底泥稳定化固化处理技术的研究,研究了不同添加比的水泥对砾砂质和黏质底泥中重金属的无害化处理效果及规律,介绍了固化稳定化工艺流程和设备,可供国内同类工程项目借鉴。     

南淝河底泥中氮磷空间分布规律及污染评价

为了研究合肥市南淝河底泥中总氮、总磷的污染状况,在南淝河及支流选取22个取样断面采集底泥柱状样,并分别利用碱性过硫酸钾消化紫外比色法和酸性过硫酸钾消化接钼锑抗比色法对总氮(TN)和总磷(TP)含量进行测定,并分析其空间分布规律。研究结果表明:南淝河底泥中氮、磷的含量随着深度的增加而减小,且总氮和总磷的各级断面上的含量与《全国河流湖泊水库底泥污染状况调查评价》研究报告中的数据相比,含量明显全国平均水平,属于生态危险区。     

Effect of calcium on adsorption capacity of powdered activated carbon

We investigated the effect of calcium ion on the adsorption of humic acid (HA) (as a target pollutant) by powered activated carbon. The HA adsorption isotherms at different pH and kinetics of two different solutions including HA alone and HA doped Ca²⁺, were performed. It was showed that the adsorption capacity of powdered activated carbon (PAC) for HA was markedly enhanced when Ca²⁺ was doped into HA. Also, HA and Ca²⁺ taken as nitrate were tested on the uptake of each other respectively and it was showed that the adsorbed amounts of both of them were significantly promoted when HA and calcium co-existed. Furthermore, the adsorbed amount of HA slightly decreased with the increasing of Ca²⁺ concentration, whereas the amount of calcium increased with the increasing of HA concentration, but all above the amounts without addition. Finally, the change of pH before and after adsorption process is studied. In the two different solutions including HA alone and HA doped Ca²⁺, pH had a small rise, but the extent of pH of later solution was bigger.     

Application of hinokitiol potassium salt for wood preservative

The decay of wood and other cellulosic materials by fungi cause significant economic loss. The widely used chromated copper arsenate was prohibited for the environmental impact and safety of arsenic and chromium. It was found that natural product hinokitiol (HK) had fungicidal and insecticidal activities, and its toxicity was bearable for the environment. We described the practical synthesis of HK-K salt. According to the GB/T18261-2000 and LY/T1283-1998, wood preservative performance of HK-K salt was tested. The results showed that the best inhibitory concentration of HK-K salt was 50 mg/L, for which the prevention effectiveness on mold is better, the killed value is between 0 and 1, and the corrosion-resistant for wood-rotting fungi is grade A.     

Porous FeOx/BiVO4-δS0.08：Highly efficient photocatalysts for the degradation of Methylene Blue under visible-light illumination

Porous S-doped bismuth vanadate with an olive-like morphology and its supported iron oxide （y wt.% FeOx/BiVO4-δS0.08, y = 0.06, 0.76, and 1.40） photocatalysts were fabricated using the dodecylamine-assisted alcohol-hydrothermal and incipient wetness impregnation methods, respectively. It is shown that the y wt.% FeOx/BiVO4-δS0.08 photocatalysts contained a monoclinic scheetlite BiVO4 phase with a porous olive-like morphology, a surface area of 8.8-9.2 m^2/g, and a bandgap energy of 2.38-2.42 eV. There was co-presence of surface Bi^5＋, Bi^3＋, V^5＋, V^3＋, Fe^3＋, and Fe^2＋ species in y wt.% FeOx/BiVO4-δS0.08. The 1.40 wt.% FeOx/BiVO4-δS0.08 sample performed the best for Methylene Blue degradation under visible-light illumination. The photocatalytic mechanism was also discussed. We believe that the sulfur and FeOx co-doping, higher oxygen adspecies concentration, and lower baudgap energy were responsible for the excellent visible-light-driven catalytic activity of 1.40 wt.% FeOx/BiVO4-δS0.08.