UV/H2O2 oxidation of tri(2-chloroethyl) phosphate: Intermediate products, degradation pathway and toxicity evaluation

Tri(2-chloroethyl) phosphate(TCEP) with the initial concentration of 5 mg/L was degraded by UV/H₂O₂ oxidation process. The removal rate of TCEP in the UV/H₂O₂ system was 89.1% with the production of Cl-and PO₄^3- of 0.23 and 0.64 mg/L. The removal rate of total organic carbon of the reaction was 48.8% and the pH reached 3.3 after the reaction. The oxidative degradation process of TCEP in the UV/H₂O₂ system ...     

A review of gas-phase chemical mechanisms commonly used in atmospheric chemistry modelling

The atmospheric chemical mechanism is an essential component of airshed models used for investigating the chemical behaviors and impacts of species. Since the first tropospheric chemical mechanism was proposed in the 1960s, various mechanisms including Master Chemical Mechanism (MCM), Carbon Bond Mechanism (CBM), Statewide Air Pollution Research Center (SAPRC) and Regional Atmospheric Chemistry Mechanism (RACM) have been developed for different research purposes. This work summarizes the development and applications of these mechanisms, introduces their compositions and lumping methods, and compares the ways the mechanisms treat radicals with box model simulations. CBM can reproduce urban pollution events with relatively low cost compared to SAPRC and RACM, whereas the chemical behaviors of radicals and the photochemical production of ozone are described in detail in RACM. The photolysis rates of some oxygenated compounds are low in SAPRC07, which may result in underestimation of radical levels. As an explicit chemical mechanism, MCM describes the chemical processes of primary pollutants and their oxidation products in detail. MCM can be used to investigate certain chemical processes; however, due to its large size, it is rarely used in regional model simulations. A box model case study showed that the chemical behavior of OH and HO₂ radicals and the production of ozone were well described by all mechanisms. CBM and SAPRC underestimated the radical levels for different chemical treatments, leading to low ozone production values in both cases. MCM and RACM are widely used in box model studies, while CBM and SAPRC are often selected in regional simulations.     

等离子体催化降解甲苯途径的原位红外研究

考察了在常温常压条件下,等离子体分别协同SiO₂、Al₂O₃、NiO/Al₂O₃降解甲苯的性能,并从材料的介电常数、对甲苯的吸附性及臭氧分解能力等角度分析了不同活性表现的原因,同时,采用原位红外技术研究了甲苯降解过程中催化剂表面吸附物种的变化.结果表明,当甲苯浓度为100 ppm,气体流量为100 mL·min^-1时,一定范围内,甲苯降解率随着能量密度、介电常数、吸附性及臭氧分解能力的提高而提高.甲苯在催化剂表面的吸附对其降解途径有十分重要的影响:在放电区域中加入SiO₂,甲苯仍然在气相中完成降解;而存在Al₂O₃ 及NiO/Al₂O₃时,甲苯氧化成苯甲酸的过程主要发生在催化剂表面,是甲苯催化降解的关键步骤,苯甲酸在活性位点的积累将降低催化剂的反应活性.     

An online monitoring system for atmospheric nitrous acid (HONO) based on stripping coil and ion chromatography

A new instrument for measuring atmospheric nitrous acid(HONO) was developed,consisting of a double-wall glass stripping coil sampler coupled with ion chromatography(SC-IC).SC-IC is featured by small size(50 × 35 × 25 cm) and modular construction,including three independent parts:the sampling unit,the transfer and supporting unit,and the detection unit.High collection efficiency(> 99%) was achieved with 25 μmol/L Na2CO3 as absorption solution even in the presence of highly acidic compounds.This instrument has a detection limit of 8 pptv at 15 min time resolution,with a measurement uncertainty of 7%.Potential interferences from NOx,NO2+SO2,NO2+VOCs,HONO+O3,HNO3,peroxyacetyl nitrite(PAN) and particle nitrite were quantified in laboratory studies and were found to be insignificant under typical atmospheric conditions.Within the framework of the 3C-STAR project,inter-comparison between the SC-IC and LOPAP(long path liquid absorption photometer) was conducted at a rural site in the Pearl River Delta.Good agreement was achieved between the two instruments over three weeks.Both instruments determined a clear diurnal profile of ambient HONO concentrations from 0.1 to 2.5 ppbv.However,deviations were found for low ambient HONO concentrations(i.e.< 0.3 ppbv),which cannot be explained by previous investigated interference species.To accurately determine the HONO budget under illuminated conditions,more intercomparison of HONO measurement techniques is still needed in future studies,especially at low HONO concentrations.     

NOx光解测量装置的设计与测试

根据二氧化氮的光解反应原理,自主设计、装配了一套氮氧化物光解反应装置,并将其与Thermo 42系列氮氧化物分析仪的化学发光检测室联用,进行了不同条件下(分别为标气流量、臭氧流量、光源温度、功率、样品湿度)NO2光解转化效率的测试.结果表明:进样流量为100~200 mL·min-1、光源温度为20℃、光源功率约为60 W(光密度约26 W·mL-1)的条件下,可得到较高的光解转化效率(约80%);臭氧流量及样品相对湿度对转化效率影响不大.在上述最佳转化效率的条件下,将其与PLC860-CLD88p(ECO PHYSICIS)进行了为期8 d的比对实验.结果显示:二者的NO2实际测量结果趋势基本一致:[NO2]ECO=0.908×[NO2]PKU+1.913(R2=0.955),初步证实了该套自主设计光解装置应用于实际观测的可靠程度.     

潮滩沉积物重金属污染的色度反演方法初探

为了探求快速评估土壤重金属污染的方法,以崇明岛东滩低、中、高潮滩沉积物为研究对象,用色度仪测量其色度参数(明度L*、红度a*、黄度b*),并对照化学分析数据,初步探讨了潮滩沉积物的色度特征与重金属元素(Cu、Cr、 Pb、Zn、Mn、Fe )含量之间的相关关系.同时,运用回归分析分别建立了重金属元素含量与色度参数（明度L*、红度a*、黄度b*）之间的定量关系模型,并对模型进行验证.结果表明,在崇明岛低、中、高潮滩的沉积物中,Cu、Pb、Zn与L*之间负相关,相关系数最高可达rCu=-0.97、 rPb= -0.88、 rZn=-0.98;Cu、Pb、Zn与a*之间正相关;而Cr与a*之间负相关.在河口水体中重金属含量稳定的条件下,色度信息可以定量地反演潮滩沉积物重金属元素的含量,为大范围的潮滩重金属污染研究提供了一项实用有效的辅助手段.     

催化湿式氧化预处理造纸黑液

采用连续式固定床反应器,利用自制稀土类复合金属氧化物催化剂对草浆造纸黑液进行了催化湿式氧化(CWAO)预处理研究.通过正交实验确定了最佳工艺条件为:进水COD 40 800 mg/L,空速0.8h-1,反应温度260℃,反应压力6.5 MPa.在此最佳条件下进行实验,COD去除率达90％.经CWAO工艺处理后,草浆造纸...     

固定源稀释通道的设计和外场测试研究

为研究固定源产生的颗粒物的污染情况,自行设计了固定源稀释通道采样装置以便模拟颗粒物在大气中的稀释扩散过程.该装置采用不同尺寸的采样嘴,以保证对烟道内的颗粒物等速采样,采样烟气与洁净空气在稀释腔内混合,腔内雷诺数典型值可以达到10000,保证了采样烟气和洁净空气能够稀释混合均匀.颗粒物在停留室中的停留时间达到90s,保证了颗粒物有足够的时间长大成核.将该装置应用于国内的9个燃煤、燃油固定源,取得了颗粒物的质量浓度、OC、EC组成、排放因子等数据.     

北京市大气细粒子的来源分析

细粒子(空气动力学直径小于2.5μm的颗粒物)污染是许多城市重要的大气环境问题.从1999年至2000年对北京市细粒子展开了4次采样和化学分析,有效采样天数为40d.利用正定矩阵分解(PMF)方法对细粒子的来源进行了分析.化学成分包括EC(元素碳)、有机物、SO₄^2-、F^-、Cl^-、Fe、Ca、K、Mg、Al、Na、Zn、Mn、Ti、Pb、Ba和P等17种.发现主要来源有6类:地面扬尘、建筑源、生物质燃烧、二次源、机动车排放和燃煤.     

在降雨量极少的条件下日本琵琶湖的环境因子的分布(英文)

琵琶湖是日本第一大淡水湖,20世纪60年代以来,由于经济的发展,湖水水质逐步变坏。1977年湖的北部出现赤潮,1983年湖的南部出现了湖泊富营养化的产物微囊藻。多年来,在深水区湖水温度分层情况下,叶绿素a或浮游植物主要分布在湖的表层(Tezuka,1984)。但在1994年夏季,降雨量极少的情况下,在深水区叶绿素a或浮游植物主要分布在温跃层附近,这种现象在琵琶湖是罕见的(Nakanishi,1995)。最近,琵琶湖北湖的藻类爆发显著增加了溶氧的消耗,导致了湖底层溶氧的减少。如果湖底层溶氧持续减少,底泥储存的磷就会释放到湖水中,从而加快湖泊富营养化的进程。本文分析了琵琶湖南北10个点1994年4月至1995年3月每月1次的常规观测资料,深入剖析了全湖物理化学参数的时空分布,不仅发现叶绿素的峰值在湖水温度分层时出现在温跃层的上部,而且湖底边界层同时出现了低溶氧和高浊度的现象。分析认为绿素a和溶氧、浊度的对应关系表明温跃层是一光合成活跃的区间。