Occurrence and distribution of hexabromocyclododecane in sediments from seven major river drainage basins in China

The concentrations and geographical distribution of hexabromocyclododecane (HBCD) were investigated in 37 composite surface sediments from seven major river drainage basins in China, including Yangtze River, Yellow River, Pearl River, Liaohe River, Haihe River, Tarim River and Ertix River. The detection frequency of HBCD was 54%, with the concentrations ranged from below limit of detection (LOD) to 206 ng/g dry weight. In general, the geographical distribution showed increasing trends from the upper reaches to the lower reaches of the rivers and from North China to Southeast China. Compared to other regions in the world, the average concentration of HBCD in sediments from Yangtze River drainage basin was at relatively high level, whereas those from other six river drainage basins were at lower or similar level. The highest HBCD concentration in sediment from Yangtze River Delta and the highest detection frequency of HBCD in Pearl River drainage basins suggested that the industrial and urban activities could evidently affect the HBCD distribution. HBCD diastereoisomer profiles showed that γ-HBCD dominated in most of the sediment samples, followed by α- and β-HBCD, which was consistent with those in the commercial HBCD mixtures. Further risk assessment reflected that the average inventories of HBCD were 18.3, 5.87, 3.92, 2.50, 1.77 ng/cm 2 in sediments from Pearl River, Haihe River, Tarim River, Yellow River and Yangtze River, respectively.     

太湖流域典型河流沉积物重金属污染特征及生态风险评价

武宜运河位于太湖西部贯穿大部分太湖入湖河流,其重金属污染的研究,对太湖重金属污染来源,流域管理具有重要的意义。因此,2012年8月对武宜运河全程底质调查,分析了沉积物中Cu、Zn、Pb、Ni、Cr等元素,通过地累积指数评价、相关分析、潜在生态风险评价以及相关研究对比分析,得出以下结论:1)Cu、Zn、Pb、Ni、Cr污染浓度均值为129.38,207.74,52.13,28.26,77.06 mg/kg,其中Cu、Zn、Pb、Ni、Cr均超过毒性参考值(TRV),Cu超标达800%。Zn、Pb、Cr在世界湖泊沉积物中微量金属的范围(WCTMEL)内,Cu超出144%,Ni略低于WCTMEL;2)Ni-Cr、Zn-Pb具有较好的同源性。且Cu、Zn污染较高,达到"中—强"和"强"污染级别,Pb污染级别其次,Ni、Cr污染级别较低或无污染。可以排除武宜运河携带Ni、Cr污染物进入入湖河网的可能;3)Cu为武宜运河生态风险主要贡献因子。需加强工业园区地段重金属污染控制,减少污染来源,加大武宜运河对连同入湖水系的清水补充。     

悬浮膜(CFM)分离技术在油田废水处理中的应用

应用微电解等技术对油田废水进行预处理,然后用悬浮膜进行分离,使其中的油、微生物和固体物与水相分离,使其达到回注用水要求。重点对CFM分离设备的结构及原理加以介绍,以期推进过滤技术的进步,提高油田废水的处理水平。     

A pilot-scale study of cryolite precipitation from high fluoride-containing wastewater in a reaction-separation integrated reactor

Fluoride removal by traditional precipitation generates huge amounts of a water-rich sludge with low quality, which has no commercial or industrial value. The present study evaluated the feasibility of recovering fluoride as low water content cryolite from industrial fluoride-containing wastewater. A novel pilot-scale reaction-separation integrated reactor was designed. The results showed that the seed retention time in the reactor was prolonged to strengthen the induced crystallization process. The particle size of cryolite increased with increasing seed retention time, which decreased the water content. The recovery rate of cryolite was above 75% under an influent fluoride concentration of 3500 mg/L, a reaction temperature of 50℃, and an influent flow of 40 L/hr. The cryolite products that precipitated from the reactor were small in volume, large in particle size, low in water content, high in crystal purity, and recyclable.     

以废气为热源生产二水氯化钙的新工艺

针对在氯化法生产钛白粉的过程中产生的大量高热值废气和氯化钙废水,提出以废气为热源生产二水氯化钙的新工艺。以焚烧的方式处理氯化尾气,将产生的热量用于浓缩蒸发氯化钙废水,生产工业级二水氯化钙产品,达到以废治废的目的。不仅处理了工业废气和废水,在节约能源的同时创造了一定的经济效益。     

Competitive sorption between 17α-ethinyl estradiol and bisphenol A/4-n-nonylphenol by soils

The sorption of 17α-ethinyl estradiol(EE2),bisphenol A(BPA),and 4-n-nonylphenol(NP) in single systems and the sorption of EE2 with different initial aqueous concentrations of BPA or NP were examined using three soils.Results showed that all sorption isotherms were nonlinear and fit the Freundlich model.The degree of nonlinearity was in the order BPA(0.537-0.686) > EE2(0.705-0.858) > NP(0.875-0.0.951) in single systems.The isotherm linearity index of EE2 sorption calculated by the Freundlich model for Loam,Silt Loam and Silt increased from 0.758,0.705 and 0.858,to 0.889,0.910 and 0.969,respectively,when BPA concentration increased from 0 to 1000 μg/L,but the effect of NP was comparably minimal.Additionally,EE2 significantly suppressed the sorption of BPA,but insignificantly suppressed that of NP.These findings can be attributed to the difference of sorption affinity of EE2,NP and BPA on the hard carbon(e.g.,black carbon) of soil organic matter that dominated the sorption in the low equilibrium aqueous concentration range of endocrine-disrupting chemicals(EDCs).Competitive sorption among EDCs presents new challenges for predicting the transport and fate of EDCs under the influence of co-solutes.     

Effect of ammonium on nitrous oxide emission during denitrification with different electron donors

Nitrous oxide(N2O) emission during denitrification is receiving intensive attention due to its high potential to cause greenhouse effects.In this study,denitrifiers were acclimated in sequencing batch reactors with methanol or acetate as the electron donor and nitrate as the electron acceptor.The effects of ammonium on N2O emission were examined in batch experiments with various electron donors.With the addition of ammonium,N2O emission increased under all the examined conditions compared to experiments without ammonium addition.With different electron donors,the highest ratio of N2O emission to the removed oxidized nitrogen was 0.70% for methanol,5.34% for acetate,and 34.79% for polyhydroxybutyrate.     

Enhanced photocatalytic activity of quantum-dot-sensitized one-dimensionally-ordered ZnO nanorod photocatalyst

An efficient photocatalyst was fabricated by assembling quantum dots （QDs） onto one-dimensionally-ordered ZnO nanorods, and the photocatalytic properties for Methyl Orange degradation were investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, UV-Vis-NIR absorption spectroscopy and photoluminescence. The results indicate that the catalyst with assembled QDs is more favorable for the degradation than the pristine ZnO nanorods. The QDs with core-shell structure lower the photocatalytic ability due to the higher carder transport barrier of the ZnS shell layer. Besides its degradation efficiency, the photocatalyst has several advantages given that the one-dimensionally-ordered ZnO nanorods have been grown directly on indium tin oxide substrates. The article provides a new method to design an effective and easily recyclable photocatalyst.     

Simultaneous preconcentration of cadmium and lead in water samples with silica gel and determination by flame atomic absorption spectrometry

A new method that utilizes pretreated silica gel as an adsorbent has been developed for simultaneous preconcentration of trace Cd(II) and Pb(II) prior to the measurement by flame atomic absorption spectrometry. The effects of pH, the shaking time, the elution condition and the coexisting ions on the separation/preconcentration conditions of analytes were investigated. Under optimized conditions, the static adsorption capacity of Cd(II) and Pb(II) were 45.5 and 27.1mg/g, the relative standard deviations were 3.2% and 1.7% (for n = 11), and the limits of detection obtained were 4.25 and 0.60 ng/mL, respectively. The method was validated by analyzing the certified reference materials GBW 07304a (stream sediment) and successfully applied to the analysis of various treated wastewater samples with satisfactory results.     

Adsorption of Cr(Ⅲ) from acidic solutions by crop straw derived biochars

Cr（Ⅲ） adsorption by biochars generated from peanut, soybean, canola and rice straws is investigated with batch methods. Adsorption of Cr（Ⅲ） increased as pH rose from 2.5 to 5.0. Adsorption of Cr（Ⅲ） led to peak position shifts in the FFIR-PAS spectra of the biochars and made zeta potential values less negative, suggesting the formation of surface complexes between Cr^3＋ and functional groups on the biochars. The adsorption capacity of Cr（Ⅲ） followed the order： peanut straw char 〉 soybean straw char 〉 canola straw char 〉 rice straw char, which was consistent with the content of acidic functional groups on the biochars. The increase in Cr^3＋ hydrolysis as the pH rose was one of the main reasons for the increased adsorption of Cr（Ⅲ） by the biochars at higher pH values. Cr（llI） can be adsorbed by the biochars through electrostatic attraction between negative surfaces and Cr^3＋, but the relative contribution of electrostatic adsorption was less than 5%. Therefore, Cr（Ⅲ） was mainly adsorbed by the biochars through specific adsorption. The Langumir and Freundlich equations fitted the adsorption isotherms well and can therefore be used to describe the adsorption behavior of Cr（Ⅲ） by the crop straw biochars. The crop straw biochars have great adsorption capacities for Cr（Ⅲ） under acidic conditions and can be used as adsorbents to remove Cr（Ⅲ） from acidic wastewaters.