Mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor

In this study, the mercury adsorption characteristics of HBr-modified fly ash in an entrained-flow reactor were investigated through thermal decomposition methods. The results show that the mercury adsorption performance of the HBr-modified fly ash was enhanced significantly. The mercury species adsorbed by unmodified fly ash were HgCl₂, HgS and HgO. The mercury adsorbed by HBr-modified fly ash, in the entrained-flow reactor, existed in two forms, HgBr₂ and HgO, and the HBr was the dominant factor promoting oxidation of elemental mercury in the entrained-flow reactor. In the current study, the concentration of HgBr₂ and HgO in ash from the fine ash vessel was 4.6 times greater than for ash from the coarse ash vessel. The fine ash had better mercury adsorption performance than coarse ash, which is most likely due to the higher specific surface area and longer residence time.     

Remarkable promotion effect of trace sulfation on OMS-2 nanorod catalysts for the catalytic combustion of ethanol

OMS-2 nanorod catalysts were synthesized by a hydrothermal redox reaction method using MnSO₄ (OMS-2-SO₄) and Mn(CH₃COO)₂ (OMS-2-AC) as precursors. SO₄^2 −-doped OMS-2-AC catalysts with different SO₄^2 − concentrations were prepared next by adding (NH₄)₂SO₄ solution into OMS-2-AC samples to investigate the effect of the anion SO₄^2 − on the OMS-2-AC catalyst. All catalysts were then tested for the catalytic oxidation of ethanol. The OMS-2-SO₄ catalyst synthesized demonstrated much better activity than OMS-2-AC. The SO₄^2 − doping greatly influenced the activity of the OMS-2-AC catalyst, with a dramatic promotion of activity for suitable concentration of SO₄^2 − (SO₄/catalyst = 0.5% W/W). The samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectroscopy (ICP-OES), NH₃-TPD and H₂-TPR techniques. The results showed that the presence of a suitable amount of SO₄^2 − species in the OMS-2-AC catalyst could decrease the Mn–O bond strength and also enhance the lattice oxygen and acid site concentrations, which then effectively promoted the catalytic activity of OMS-2-AC toward ethanol oxidation. Thus it was confirmed that the better catalytic performance of OMS-2-SO₄ compared to OMS-2-AC is due to the presence of some residual SO₄^2 − species in OMS-2-SO₄ samples.     

Insights into metals in individual fine particles from municipal solid waste using synchrotron radiation-based micro-analytical techniques

Excessive inter-contamination with heavy metals hampers the application of biological treatment products derived from mixed or mechanically-sorted municipal solid waste(MSW). In this study, we investigated fine particles of 2 mm, which are small fractions in MSW but constitute a significant component of the total heavy metal content, using bulk detection techniques. A total of 17 individual fine particles were evaluated using synchrotron radiation-based micro-X-ray fluorescence and micro-X-ray diffraction. We also discussed the association, speciation and source apportionment of heavy metals. Metals were found to exist in a diffuse distribution with heterogeneous intensities and intense hot-spots of 10 μm within the fine particles. Zn–Cu, Pb–Fe and Fe–Mn–Cr had significant correlations in terms of spatial distribution. The overlapped enrichment, spatial association, and the mineral phases of metals revealed the potential sources of fine particles from size-reduced waste fractions(such as scraps of organic wastes or ceramics) or from the importation of other particles. The diverse sources of heavy metal pollutants within the fine particles suggested that separate collection and treatment of the biodegradable waste fraction(such as food waste) is a preferable means of facilitating the beneficial utilization of the stabilized products.     

Effect of AlCl3 concentration on nanoparticle removal by coagulation

In recent years, engineered nanoparticles, as a new group of contaminants emerging in natural water, have been given more attention. In order to understand the behavior of nanoparticles in the conventional water treatment process, three kinds of nanoparticle suspensions, namely multi-walled carbon nanotube-humic acid (MWCNT-HA), multi-walled carbon nanotube-N,N-dimethylformamide (MWCNT-DMF) and nanoTiO₂-humic acid (TiO₂-HA) were employed to investigate their coagulation removal efficiencies with varying aluminum chloride (AlCl₃) concentrations. Results showed that nanoparticle removal rate curves had a reverse “U” shape with increasing concentration of aluminum ion (Al^3 +). More than 90% of nanoparticles could be effectively removed by an appropriate Al^3 + concentration. At higher Al^3 + concentration, nanoparticles would be restabilized. The hydrodynamic particle size of nanoparticles was found to be the crucial factor influencing the effective concentration range (ECR) of Al^3 + for nanoparticle removal. The ECR of Al^3 + followed the order MWCNT-DMF > MWCNT-HA > TiO₂-HA, which is the reverse of the nanoparticle size trend. At a given concentration, smaller nanoparticles carry more surface charges, and thus consume more coagulants for neutralization. Therefore, over-saturation occurred at relatively higher Al^3 + concentration and a wider ECR was obtained. The ECR became broader with increasing pH because of the smaller hydrodynamic particle size of nanoparticles at higher pH values. A high ionic strength of NaCl can also widen the ECR due to its strong potential to compress the electric double layer. It was concluded that it is important to adjust the dose of Al^3 + in the ECR for nanoparticle removal in water treatment.     

低浓度苯系物在新疆干旱区土壤中的吸附行为研究

采集新疆干旱区石化废水库附近区域土壤,以苯、甲苯、乙苯、二甲苯(间、对二甲苯)等典型苯系物为研究对象,系统研究低浓度苯系物在干旱区土壤上的吸附行为,分析土壤有机质含量,溶液p H、溶液含盐量、温度对苯系物吸附的影响。结果显示土壤对低浓度苯系物的吸附16 h达到平衡;吸附等温线经拟合后符合Henry直线型吸附模型;土壤对苯系物的吸附量随着土壤有机质含量的增加而增加,土壤有机质含量与吸附量呈显著正相关(P0.01,R2≥0.919);溶液p H值对吸附过程无明显作用;随着溶液含盐量增大,土壤对苯系物的吸附量表现为先减小,再稳定;温度升高会抑制土壤对苯系物的吸附作用。     

四川三岔湖重金属污染与人类活动的关系

沉积物对湖泊重金属污染具有指示作用,通过分析沉积物的污染特征可以揭示湖泊重金属污染的污染历史和污染源。利用210Pb和137Cs定年和沉积物粒度分析,研究了三岔湖沉积物重金属的不同湖区和不同年代的分布特征及形成原因。人类活动强烈影响了重金属的沉积与富集:Cu、Zn与网箱养殖密切相关,Pb则主要源于邻近岸区的交通运输活动,Cr主要来自农业面源污染。受自身化学特性的影响,重金属的含量与沉积物的粒度分布密切相关,也正因此会出现洪水等的特殊年份重金属污染特征的异变。     

闸控河段水质浓度影响关键因子识别

由于闸门调度对河道内的水环境要素具有强烈的扰动作用,故闸控河段的水质变化过程较常规河道更为复杂。为了探析引起闸控河段水质浓度变化的主要制约因素,以槐店闸为研究对象,结合笔者进行的2次实验和其他时期的监测数据,通过偏相关分析和主成分分析的方法识别影响闸控河段水质浓度变化的关键因子,并利用多元线性回归方法分析得到闸控河段水质浓度变化与其关键因子的多元线性回归方程。经过分析初步得到,与高锰酸盐指数浓度变化率有关的关键因子为闸门开度、开启个数、高锰酸盐指数来水浓度、溶解氧含量、流速和水深;与氨氮浓度变化率有关的关键因子为闸门开度、开启个数、氨氮来水浓度、溶解氧含量和p H值。     

再生水消毒副产物去除技术研究进展

三卤甲烷、卤乙酸、卤乙腈、三氯硝基甲烷以及N-亚硝基二甲胺是再生水氯/氯胺消毒中主要的消毒副产物,具有较强的毒性和致癌性,严重威胁生态安全及人体健康。目前难以通过改变消毒条件来减少其生成量,而去除其前驱物可有效降低消毒副产物的生成。文章介绍了氧化法、混凝沉淀法、离子交换法以及膜过滤等方法去除消毒副产物前驱物的研究,重点分析了臭氧氧化法去除消毒副产物前驱物的影响因素,对已生成的消毒副产物的去除也进行了简述。     

两种方法测定固定污染源废气中铅的对比研究

以石英纤维滤筒采样,采用硝酸-氢氟酸消解体系,建立了火焰原子吸收光谱法和电感耦合等离子体原子发射光谱法测定固定污染源废气中铅的分析方法。分别对两种方法的波长选择、干扰因素、标准曲线、检出限、准确度和精密度等方面进行了对比研究,并对两种方法的测定结果进行t检验。结果表明,两种方法无显著性差异,均可用于固定污染源废气中铅的含量测定。     

秦皇岛市主要陆源入海排污口污染现状评价

根据2011年对秦皇岛周边海域环境影响较大的11个陆源入海排污口的调查结果,通过单因子污染指数及等标污染负荷相关指标的计算,分析评价秦皇岛市主要入海排污口(河流)的污染现状及主要污染源。调查结果表明,区域内所有排污口中,大蒲河排污口的污染负荷比最大;其次为滦河、新开河;所有调查指标中,总磷的污染负荷比最大,是秦皇岛近岸海域最主要的污染物。