有机物料添加对植物修复铬污染土壤的影响

为探讨有机物料添加对植物修复铬污染耕地土壤的强化效果,在联栋温室中进行室内培养试验和盆栽试验,利用Tessier连续提取法对添加牛粪、羊粪和玉米秸秆后的土壤中铬形态分布进行分析.通过S-N-K法、Pearson相关分析等研究添加有机物料后,紫羊茅和羽衣甘蓝对修复土壤的铬富集系数及铬去除率的影响,并探讨其与铬形态间的相互关系.结果表明,添加牛粪或羊粪的土壤中交换态铬分别比空白处理增加1.30％和0.98％.添加牛粪可显著提高紫羊茅和羽衣甘蓝的根干重和茎叶干重,添加羊粪或玉米秸秆仅可显著提高富集植物的茎叶干重,对根干重无显著影响.添加羊粪或牛粪处理的紫羊茅和羽衣甘蓝,修复土壤的铬富集系数均显著高于空白处理.添加玉米秸秆紫羊茅修复土壤的铬富集系数显著高于空白处理,羽衣甘蓝修复土壤的铬富集系数与空白处理无显著差异.3种有机物料的添加均能增强羽衣甘蓝和紫羊茅对铬污染土壤的修复效果,其中添加牛粪诱导强化羽衣甘蓝修复铬污染土壤的效果最佳,对土壤中铬的去除率达到19.62％.紫羊茅和羽衣甘蓝修复土壤的铬富集系数及铬去除率均与土壤交换态铬显著正相关,与碳酸盐结合态铬比例呈极显著负相关.有机物料,尤其是养殖废弃物的添加,能有效提高土壤中可交换态铬比例,进而提高植物修复铬污染土壤的效率.     

应用Modified Gompertz模型对城市生活垃圾沼气发酵的拟合研究

尽管Modified Gompertz模型与料菌比和发酵浓度之间没有直接的函数和变量关系,但是料菌比和浓度的变化必然导致Modified Gompertz模型参数的改变,因此可以通过Modified Gompertz模型参数的变化特征对料菌比和发酵浓度是否适宜作出合理的评价.据此本研究将采用中温批量发酵,分别设计单因素...     

地表水中有机污染物的化学需氧量的探讨与研究

有机污染物对地表水的危害主要表现在自身氧化过程对水中溶解氧的消耗,化学需氧量（COD）是评定水中耗氧有机物含量的指标之一,本文主要研究讨论了化学需氧量指标并具体阐述了几种检测方法。     

胜利原油对半滑舌鳎幼鱼肝脏谷胱甘肽过氧化物酶和谷胱甘肽转硫酶活性的影响

在实验室条件下研究了不同浓度胜利原油暴露1、2、4、8、15d以及解除污染1d和3d后对半滑舌鳎幼鱼肝脏谷胱甘肽过氧化物酶( GSH-PX)和谷胱甘肽转硫酶(GST)活性的影响.结果表明:曝油15d内,各浓度组GSH-PX活性呈峰值变化,先增大后减小,第4d时升高到最大值,其中3.2 mg/L组在第1d就被显著诱导(P...     

活性炭物化性质对吸附天然水体中有机污染物的影响

研究了天然水体条件下2种合成有机污染物(SOC)甲基对硫磷(MP)和三氯乙烯(TCE)以及天然有机物(NOM)在5种粉末活性炭(PAC)上的吸附特性.在对活性炭的物化特性进行全面表征的基础上,利用相关分析方法揭示了PAC的物理和化学性质对天然水体中SOC类小分子有机污染物吸附的影响;并利用高效体积排阻色谱法(HPSEC...     

聚糖原菌富集实验及其内源过程探究

细胞衰减是微生物内源过程的一个重要组成部分,可分为由细胞死亡引起的数量衰减和由细胞活性降低引起的活性衰减两部分.通过挥发性脂肪酸（VFA）吸收速率(VFAUR)测定、荧光原位杂交技术（FISH）以及LIVE/DEAD细胞染色技术,研究了富集聚糖原菌（GAOs）在序批式反应器（SBR）系统中好氧环境下的衰减特征.结果表明,当T=30℃、进料中m(COD)∶m(P)=100时,SBR系统中GAOs富集比例达94%.测定和计算表明,SBR富集系统中GAOs衰减速率和死亡速率分别为0.132 d^-1和0.034 d^-1,其数量衰减和活性衰减占其细胞总衰减比例分别为26%和74%.可见,GAOs数量衰减只占其细胞总衰减中很小一部分,而绝大部分衰减由活性衰减所引起.     

浸入式短流程超滤膜生产工艺过程膜污染的形成与控制

以江苏芦泾水厂膜技术改造工程为对象,从水质、膜工艺特征结合生产运行过程以及污染膜的清洗进行了分析,目的是了解膜污染的组分构成,评价不同清洗剂的清洗效果,获取较优的清洗顺序.结果表明,原水以憎水酸(HOA)和亲水组分(HIM)为主体,质量分数各占40.34%和28.48%.溶解性有机物(DOM)则以芳香性蛋白质Ⅱ类物质为...     

太湖沉积物酸可挥发性硫化物分布特征及重金属生物有效性评价

对太湖4个湖区沉积物的酸可挥发性硫化物（AVS）和同步可提取重金属（SEM）的水平和垂直分布特征进行了研究,并对沉积物重金属的潜在生态风险进行初步评价.结果表明,氧化还原电位（Eh）与AVS和SEM含量均无显著相关性;表层沉积物中AVS含量分布在研究区差异较大,变异系数达134.28%;∑SEM含量波动较小,变异系数为...     

Reversibly enhanced aqueous solubilization of volatile organic compounds using a redox-reversible surfactant

Surfactant-enhanced remediation (SER) is an effective method for the removal of volatile organic compounds (VOCs) from contaminated soils and groundwater. To reuse the surfactant the VOCs must be separated from the surfactant solutions. The water solubility of VOCs can be enhanced using reversible surfactants with a redox-acive group, (ferrocenylmethyl)dodecyldimethylammonium bromide (Fcl2) and (ferrocenylmethyl)tetradecanedimethylammonium bromide (Fcl4), above and below their critical micelle concentrations (CMC) under reducing (I⁺) and oxidative (I²⁺) conditions. The CMC values of Fcl2 and Fcl4 in I⁺ are 0.94 and 0.56 mmol/L and the solubilization of toluene by Fcl2 and Fcl4 in I⁺ for toluene is higher than the solubilization achieved with sodium dodecyl sulfate, cetyltrimethylammonium bromide and Trition X-114. The solubilization capacity of the ferrocenyl surfactants for each tested VOCs ranked as follows: ethylbenzene > toluene > benzene. The solubilities of VOCs by reversible surfactant in I⁺ were 30% higher than those in I²⁺ at comparable surfactant concentrations. The effects of Fcl4 concentrations on VOCs removal efficiency were as follows: benzene > toluene > ethylbenzene. However, an improved removal efficiency was achieved at low ferrocenyl surfactant concentrations. Furthermore, the reversible surfactant could be recycled through chemical approaches to remove organic pollutants, which could significantly reduce the operating costs of SER technology.     

Transport and fate of mercury under different hydrologic regimes in polluted stream in mining area

Seepage from Hg mine wastes and calcines contains high concentrations of mercury (Hg). Hg pollution is a major environmental problem in areas with abandoned mercury mines and retorting units. This study evaluates factors, especially the hydrological and sedimentary variables, governing temporal and spatial variation in levels and state of mercury in streams impacted by Hg contaminated runo . Samples were taken during di erent flow regimes in theWanshan Hg mining area in Guizhou Province, China. In its headwaters the sampled streams/rivers pass by several mine wastes and calcines with high concentration of Hg. Seepage causes serious Hg contamination to the downstream area. Concentrations of Hg in water samples showed significant seasonal variations. Periods of higher flow showed high concentrations of total Hg (THg) in water due to more particles being re-suspended and transported. The concentrations of major anions (e.g., Cl??, F??, NO3?? and SO4 2??) were lower during higher flow due to dilution. Due to both sedimentation of particles and dilution from tributaries the concentration of THg decreased from 2100 ng/L to background levels (< 50 ng/L) within 10 km distance downstream. Sedimentation is the main reason for the fast decrease of the concentration, it accounts for 69% and 60% for higher flow and lower flow regimes respectively in the upper part of the stream. Speciation calculation of the dissolved Hg fraction (DHg) (using Visual MINTEQ) showed that Hg(OH)2 associated with dissolved organic matter is the main form of Hg in dissolved phase in surface waters in Wanshan (over 95%).