A combined radical and non-radical oxidation processes for efficient degradation of Acid Orange 7 in the homogeneous Cu(II)/PMS system: important role of chloride

Environmental Science and Pollution Research - Trace copper ion (Cu(II)) in water and wastewater can trigger peroxymonosulfate (PMS) activation to oxidize organic compounds, but it only works under...     

Ionic composition of submicron particles (PM1.0) during the long-lasting haze period in January 2013 in Wuhan, central China

In January 2013, a long-lasting severe haze episode occurred in Northern and Central China; at its maximum, it covered a land area of approximately 1.4 million km². In Wuhan, the largest city in Central China, this event was the most severe haze episode in the 21st century. Aerosol samples of submicron particles (PM_1.0) were collected during the long-lasting haze episode at an urban site and a suburban site in Wuhan to investigate the ion characteristics of PM_1.0 in this area. The mass concentrations of PM_1.0 and its water-soluble inorganic ions (WSIIs) were almost at the same levels at two sites, which indicates that PM_1.0 pollution occurs on a regional scale in Wuhan. WSIIs (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, Cl^-, NO₃^- and SO₄^2-) were the dominant chemical species and constituted up to 48.4% and 47.4% of PM_1.0 at WD and TH, respectively. The concentrations of PM_1.0 and WSIIs on haze days were approximately two times higher than on normal days. The ion balance calculations indicate that the particles were more acidic on haze days than on normal days. The results of the back trajectory analysis imply that the high concentrations of PM_1.0 and its water-soluble inorganic ions may be caused by stagnant weather conditions in Wuhan.     

基于放射性碳分析的多环芳烃源解析:技术进展和准确性评估

化石燃料燃烧和生物质燃烧是污染物多环芳烃(polycyclic aromatic hydrocarbon,PAHs)的两大来源.放射性碳(14C)分析近年用于评估这两类源对环境中PAHs的相对贡献.此方法基于化石燃料和生物质的14C含量差异,即化石燃料不含14C,而生物质的14C浓度有一个较稳定值.14C的自然丰度极低(约10-12),因此检测PAHs这样的痕量污染物的14C含量一度极具挑战.1990年代中期,加速器质谱的技术突破使得对环境样品PAHs的14C分析具有实用价值.要准确测出PAHs的14C含量,须先从化学成分复杂的环境样品中分离出高纯度的PAHs.制备气相色谱因其出色的分离能力而成为目前环境样品PAHs14C分析必备的工具.本文意在简介基于14C分析的PAHs源解析的基本原理、技术进展,以及评估该方法获得的PAHs源解析结果的准确性.     

柴油机微粒中可溶性有机成分的真空干燥条件

柴油机碳烟颗粒(PM)中可溶性有机组分(SOF)含量是其重要的特性参数,而真空干燥法可方便、高效、可靠地分析颗粒SOF含量,对其干燥条件的探索具有重要的研究意义和应用价值。首先采用模拟的柴油机颗粒,分析不同的干燥条件对模拟SOF(柴油、润滑油)挥发率的影响规律,得出模拟的SOF分析的最佳干燥条件;在此基础上,探索了真实柴油机颗粒SOF分析的最佳干燥条件为:干燥温度220℃、干燥时间3 h、真空度98 kPa,得知SOF组分干燥的难易程度介于柴油和润滑油之间;同时,根据此干燥条件,分析了排气管末端采集的真实碳烟颗粒的SOF含量特性。     

Insights into the mercury(II) adsorption and binding mechanism onto several typical soils in China

To better understand the Hg(II) adsorption by some typical soils and explore the insights about the binding between Hg(II) and soils, a batch of adsorption and characteristic experiments was conducted. Results showed that Hg(II) adsorption was well fitted by the Langmuir and Freundlich. The maximum adsorption amount of cinnamon soil (2094.73 mg kg^?1) was nearly tenfold as much as that of saline soil (229.49 mg kg^?1). The specific adsorption of Hg(II) on four soil surface was confirmed by X-ray photoelectron spectroscopy (XPS) owing to the change of elemental bonding energy after adsorption. However, the specific adsorption is mainly derived from some substances in the soil. Fourier transform infrared spectroscopy (FTIR) demonstrated that multiple oxygen-containing functional groups (O–H, C=O, and C–O) were involved in the Hg(II) adsorption, and the content of oxygen functional groups determined the adsorption capacity of the soil. Meanwhile, scanning electron microscopy combined with X-ray energy dispersive spectrometer (SEM–EDS) more intuitive revealed the binding of mercury to organic matter, metal oxides, and clay minerals in the soil and fundamentally confirmed the results of XPS and FTIR to further elucidate adsorptive phenomena. The complexation with oxygen-containing functional groups and the precipitation with minerals were likely the primary mechanisms for Hg(II) adsorption on several typical soils. This study is critical in understanding the transportation of Hg(II) in different soils and discovering potential preventative measures.     

苏丹红I对小鼠卵巢的损伤作用及对Caspase-3和Ki-67表达的影响

苏丹红是一种人工合成偶氮染料,可引起肝脏及泌尿系统等多个脏器的肿瘤,但苏丹红对生殖系统的毒性研究较少。本研究以昆明小鼠为受试对象,探讨苏丹红I对小鼠卵巢组织Caspase-3和Ki-67表达的影响。将24只昆明小鼠随机分为:对照组、低剂量(60 mg·kg~(-1))、中剂量(120 mg·kg~(-1))、高剂量(240 mg·kg~(-1))4组,6只/组。胃灌4周,4周末处死。HE染色观察各组卵巢组织病理变化,免疫组化法检测卵巢组织Caspase-3和Ki-67表达,Real time PCR检测卵巢组织Caspase-3和Ki-67 m RNA表达,Western blotting检测卵巢组织中Ki-67及Caspase-3蛋白表达。与对照组比较,实验组卵巢中Caspase-3阳性细胞率显著升高(P0.05),而Ki-67阳性细胞率显著降低(P0.05),Real time PCR及Western blotting结果与免疫组化法结果一致。本实验发现苏丹红染毒后颗粒细胞的Caspase-3表达增加,且Caspase-3表达呈剂量依赖性,但Ki-67表达受到抑制。     

初始pH值对磷酸盐还原除磷的影响研究

以超高盐（盐度7％，以NaCI计）高磷榨菜废水为研究对象，考察了初始pH值对磷酸盐还原进程的影响。实验结果表明，初始pH值对磷酸盐还原除磷效能影响显著。初始pH为8时，磷酸盐还原除磷率达到最高，平均值为65．45％。同时，初始pH值还会影响污泥中活性磷的形成以及基体对磷化氢的吸附。此外，偏碱性有利于磷形态转化，且BD-P（主要是一些可溶性的、还原性强的、带有Fe-P化合物的集合）含量的高低调控着生物膜内间隙水中溶解态可反应性磷（DRP）和可还原水溶态磷（RSP）含量，最终决定着磷酸盐还原进程。随着初始pH值的升高，污泥对磷化氢的吸附能力降低导致污泥中结合态磷化氢（MBP）含量不断减少。     

高锰酸盐复合药剂强化混凝改善再生水景观湖水质研究

实验通过投加助凝剂以强化混凝沉淀过程,从而达到去除再生水景观水中的藻类。以PAC为混凝剂,高锰酸盐复合药剂(PPC)为预氧化助凝剂,通过烧杯实验确定PPC、PAC同时投加,最佳投量分别为1 mg/L、60 mg/L。生产性实验中,机械加速澄清池强化混凝对TP、叶绿素、藻密度的去除率分别为54%、32.3%和35.4%,湖水中TP、TN逐渐降低分别由4.9 mg/L、23 mg/L降至0.72 mg/L、10.3 mg/L。PPC提高了混凝沉淀对藻类的去除效果,改善了再生水景观湖水质,降低水中氮磷营养盐的含量。     

黄渤海表层沉积物中正构烷烃和甾醇的分布及来源研究

在黄海、渤海湾和莱州湾采集64个表层沉积物样品,分析正构烷烃（C15～C33）和甾醇（菜子甾醇、菜油甾醇、谷甾醇和豆甾醇）的质量分数和分子组合特征,探讨其来源,比较物质来源的空间差异。结果表明：（1）黄海表层沉积物中类脂生物标志物主要呈现陆源和海源共同影响的特征,其中北黄海以陆源输入为主,高碳数正构烷烃（〉C24）具有明显的奇碳优势,陆源高等植物的贡献较大;南黄海陆源输入与海洋自身贡献相当;渤海湾与莱州湾接受来自河流的大量陆源物质;（2）来源于陆源高等植物的甾醇（包括菜油甾醇、谷甾醇和豆甾醇）在黄海表层沉积物中的质量分数远小于渤海湾和莱州湾,但指示硅藻来源的菜子甾醇在整个研究区域均具有较高的质量分数。     

广元市次生地质灾害分布特征及影响因素分析——以朝天区为例

四川省广元市朝天区是汶川8.0级地震的重灾区之一,由地震触发的崩塌、滑坡等次生地质灾害对人民群众生命财产安全构成巨大威胁。基于实地调查,对震后地质灾害隐患点进行了统计分析,指出了地震地质灾害的分布特征,并对其影响因素进行了深入分析。区内地震地质灾害点多分布在海拔800 m以上的陡坡或陡崖部位,并沿龙门山断裂带、嘉陵江水系及交通路线呈线状或带状分布。地震地质灾害的发生是内外力共同作用结果,其中地震力和断裂构造带对地质灾害发生起着决定性的作用,而地层岩性对灾种起关键性的作用,滑坡多发育在页岩、片岩、板岩、千枚岩等软岩分布区,崩塌多发育在灰岩、砂岩等硬岩分布区。