丙烯酸柱撑类水滑石的制备及其对Cu2+的吸附性能

以Zn-Al-NO3--类水滑石为前体,采用返混沉淀法制备了丙烯酸柱撑类水滑石,将其用于吸附废水中的Cu2+.实验结果表明:当初始Cu2+质量浓度为80 mg/L、丙烯酸柱撑类水滑石加入量为40 g/L、废水pH为6、吸附时间为2.0 h时,丙烯酸柱撑类水滑石对Cu2+有较好的吸附效果,在此条件下废水中Cu2+的吸附率高达95.31％;丙烯酸柱撑类水滑石对Cu2+的吸附符合Freundlich等温吸附模型.     

不同干燥处理对城市污泥物理性质和农业利用的影响

城市污泥农用正在成为世界各国处置污泥的主要方式之一,但干燥后的污泥通常结块程度高,硬度大,较难粉碎,对污泥的后续利用产生影响.试验设置了露天、棚内浇水和棚内不浇水等三个不同的污泥干燥处理,试验结果表明,露天状态处理干燥后的污泥要明显松散,结块程度较低;露天状态处理干燥后,粒径在5～10 mm和小于5 mm的污泥颗粒含量要显著高于棚内浇水和棚内不浇水处理,且露天处理干燥后污泥中水稳性团聚体所占比例最大,小于0.001 mm的粒级(粘粒)所占比例最小,不易造成土壤板结.因此,露天处理干燥后的城市污泥对农用较为有利.     

复杂景观中营养型非点源污染物时空变异特征分析

非点源污染的形成不仅受到地表物质来源、景观格局的影响,同时还受到土壤侵蚀过程、降雨过程、灌溉过程、地表和地下水文过程的影响.由于影响非点源污染的因子复杂多样,从而导致它的时空变化较大.正确认识非点源污染的时空变异特征对于科学布设监测点和研究它的变化规律具有重要意义.本文通过野外定点监测,研究了非点源污染的时空变异.结果发现:①干旱年份各种污染物空间变异小于降雨正常年份.②对于不同污染物,无论在干旱年份还是正常年份,地表水中固体悬浮颗粒物的空间变异均较大,其他污染物的空间变异相对较小.③对于固体悬浮颗粒物,干旱年份不同水文期之间的空间变异比较接近,而正常年份的空间变异不同水文期之间差异较大.④非点源污染季节变异较小的监测点主要出现在具有稳定水源和地表径流季节变化较小的地区;而非点源污染空间变异较大的监测点主要出现在山区河流上游地表径流季节变化明显、农业用地面积较大且地表径流季节变化较大和明显受到点源污染影响的地区.     

太湖地区水稻土表层土壤10年尺度重金属元素积累速率的估计

以江苏省几个水稻土历年监测的重金属元素变化资料为基础,估计太湖地区水稻土表层土壤的重金属元素积累速率并推算本地区相应的几种环境影响的污染通量.结果表明,Cu/Zn、Pb和Cd的积累速率分别达到0.3～lmg·(kg·a)^-1、0.2～1mg·(kg·a)^-1和0.3～3μg·(kg·a)^-1,它们的年污染通量分别为0.5～1kg·(hm²·a)^-1,0.5～1.0kg·(hm²·a)^-1,0.5～3.0kg·(hm²·a)^-1和0.8～10×10^-3kg·(hm²·a)^-1.观察到有效态含量的积累速率高于全量.就整个区域来说,Pb、Cd的面源复合污染强度明显较其他环境影响因子大,尤其是Cd的污染通量较国际上的报道偏高,说明本地区环境污染较为严重,仍然是区域环境质量的制约因素本地区土壤重金属元素的变化及其对食物链的影响以及人类健康的影响必须引起广泛的重视.     

土壤中三卤甲烷(THMs)前驱物质流出的规律

通过室内模拟淋溶实验,初步探讨了以三卤甲烷生成潜能(THMFP)为指标的土壤三卤甲烷前驱物质的流出规律.结果显示:土壤淋出液中THMFP的浓度与土壤性质特别是土壤中腐殖质含量、组成与卤代活性,模拟雨水的酸度及累积淋溶量等有关.土壤中所含腐殖质的量越大、腐殖质的卤代活性越高且溶解迁移能力越强,则淋出液中THMFP的浓度越大;酸度最低(pH3.0)的模拟雨水淋洗下,淋出液中THMFP的浓度最低;模拟雨水的pH值愈低,土壤THMFP愈易流出;本实验条件下,淋出液中THMFP的浓度随累积淋溶量的增大呈下降趋势.     

Organic oxalate as leachant and precipitant for the recovery of valuable metals from spent lithium-ion batteries

Spent lithium-ion batteries containing lots of strategic resources such as cobalt and lithium are considered as an attractive secondary resource. In this work, an environmentally compatible process based on vacuum pyrolysis, oxalate leaching and precipitation is applied to recover cobalt and lithium from spent lithium-ion batteries. Oxalate is introduced as leaching reagent meanwhile as precipitant which leaches and precipitates cobalt from LiCoO(2) and CoO directly as CoC(2)O(4)·2H(2)O with 1.0 M oxalate solution at 80°C and solid/liquid ratio of 50 g L(-1) for 120 min. The reaction efficiency of more than 98% of LiCoO(2) can be achieved and cobalt and lithium can also be separated efficiently during the hydrometallurgical process. The combined process is simple and adequate for the recovery of valuable metals from spent lithium-ion batteries.     

混凝+厌氧+好氧组合工艺处理油墨废水的工程实例

采用混凝沉淀+水解酸化池+BIOFOR滤池工艺对文具厂油墨废水进行处理,通过工程实例,对工艺流程,构筑物的设计参数,调试运行进行探讨。结果表明:对于COD较大,色度非常高的油墨废水经该工艺处理后,能达到GB8978-1996《废水综合排放标准》中一级排放标准,且该工程投资小,运行费用低;管理简单方便。     

Chemical composition of the mycelium of Daldinia eschscholtzii北大核心CSCD

To investigate the chemical composition of the fungus Daldinia eschscholtzii, the compounds were separated by silica gel, Sephadex LH-20, and preparative chromatography. Their structures were identified by spectral methods. The MTT method was applied to measure the cytotoxicity of representative components. Eleven compounds were isolated and identified as 3β-hydroxyl-6,22-dien-5α,8α-peroxynitrite (1); ergosterol-9(11)-dehydroperoxide (2); mangiferonic acid (3); ergosta-4,6,8 (14),22-tetraen-3-one (4); (+)-syringaresinol (5); 3,5,3',5'-tetramethoxy-4,4,-diphenol (6); 5-methoxycoumarin (7); 5-hydroxy-2-methyl-4H-chromen-4-one (8); (2R,4R)-3,4-dihydro-5-methoxy-2-methyl-2H-1-benzopyran-4-ol (9); 2,3-dihydro-5-methoxy-2-methylchromen-4-one (10); and 7β-caruilignan C (11), respectively. Compound 4 showed inhibitory activity against H1299, H460, HGC-27, A5491, and MNK-45, with the IC50 value of 25.2 ± 2.9, 32.3 ± 4.2, 29.2 ± 1.2, 33.9 ± 3.7, and 18.0 ± 7.0 μmol/L, respectively. © 2018 Science Press. All rights reserved.     

Enhanced reductive degradation of carbon tetrachloride by carbon dioxide radical anion-based sodium percarbonate/Fe(II)/formic acid system in aqueous solution

Complete CT degradation was achieved by SPC/Fe(II)/FA system.Formic acid established the reductive circumstance by producing CO₂·^–.CO₂·^– was the dominant active species responsible for CT degradation.CT degradation was favorable in the pH range from 3.0 to 9.0.SPC/Fe(II)/FA system may be suitable for CT remediation in contaminated groundwater.The performance of sodium percarbonate (SPC) activated with ferrous ion (Fe(II)) with the addition of formic acid (FA) to stimulate the degradation of carbon tetrachloride (CT) was investigated. Results showed that CT could be entirely reduced within 15 min in the system at a variety of SPC/Fe(II)/FA/CT molar ratios in experimental level. Scavenging tests indicated that carbon dioxide radical anion (CO2·^–) was the dominant reactive oxygen species responsible for CT degradation. CT degradation rate, to a large extent, increased with increasing dosages of chemical agents and the optimal molar ratio of SPC/Fe(II)/FA/CT was set as 60/60/60/1. The initial concentration of CT can hardly affect the CT removal, while CT degradation was favorable in the pH range of 3.0–9.0, but apparently inhibited at pH 12. Cl^– and HCO₃^– of high concentration showed negative impact on CT removal. Cl^– released from CT was detected and the results confirmed nearly complete mineralization of CT. CT degradation was proposed by reductive C-Cl bond splitting. This study demonstrated that SPC activated with Fe(II) with the addition of FA may be promising technique for CT remediation in contaminated groundwater.