废水中有机污染物降解机理的研究方法

我国废水排放总量较大,且废水中含有的多种有机污染物一直是人类生命健康的潜在威胁,因此对废水处理的研究必不可少,而理解废水中有机污染物的降解机理是处理各种废水的基础.本综述概述了国内外针对各种有机污染物降解机理的研究方法,主要包括实验手段和计算模拟两大类.实验手段中主要采用光谱分析技术检测有机污染物降解过程中生成的中间产物,进而推测有机污染物的降解路径.但是由于实验条件和实验方法的不同,对于同种物质的降解机理研究,不同的实验结果存在着争议.基于量子化学计算、定量构效关系模型（QSAR）、定量结构-生物降解性能关系模型（QSBR）、统计分子碎化模型（SMF）等计算模拟方法为有机污染物降解机理的研究提供了新的方法.将实验手段和计算模拟有机结合起来,可为有机污染物的降解机理研究提供参考和指导.     

基于高分辨质谱在线观测的2011深圳大运会前后PM_1化学组成与粒径分布

本文利用先进的高分辨飞行时间气溶胶质谱仪（HR-ToF-AMS）于2011年深圳世界大学生运动会前后（2011年8月3日~9月22日）对深圳市区大气亚微米细粒子（PM1）化学成分和粒径分布进行了在线测量.结果表明,整个观测期间PM1质量浓度平均为51.1±32.6gm3,其中有机物占颗粒物总质量的37.9%,硫酸盐为37.1%,铵盐11.9%,黑碳6.6%（由一台单颗粒黑碳光度计（SP2）单独测量）,硝酸盐5.8%,氯化物0.6%.观测期间各成分（除黑碳外）的粒径分布峰值位于真空动力学粒径550nm附近,而有机物在较小粒径范围（100~200nm）仍有较多质量分布,显示出本地一次源的明显贡献.基于高分辨有机质谱计算得到的有机气溶胶的平均元素组成为：碳34.0%、氢53.2%、氧12.0%和氮0.8%（原子个数百分比）,对应的OM/OC（有机物与有机碳质量比）平均值为1.66±0.16.采用正矩阵因子解析（PMF）模型对有机气溶胶高分辨质谱进行因子解析,得到三类有机气溶胶：HOA（还原态有机气溶胶）,SV-OOA（半挥发氧化态有机气溶胶）和LV-OOA（低挥发氧化态有机气溶胶）,分别占有机物总量的31.3%,39.8%和28.9%,说明二次有机气溶胶（以SV-OOA和LV-OOA之和代表）是有机气溶胶的主体部分.结合气团来源分析不同时段PM1化学组成和粒径分布特征表明,大运会召开期间PM1质量浓度水平比整个观测期间的平均值低60.7%,是气团来自洋面等有利气象条件和黄标车限行等污染源控制措施的综合作用结果.     

海水中有机污染物的光度法测定

海水中有机污染物在强碱性条件下被KMnO4所氧化。通过对生成物溶液中K2MnO4浓度的光度法测量（λ=430nm）,直接测定海水中有机物含量（以COD表示）。该方法的线性范围为0．40—4．50mg／L（以邻苯二甲酸氢钾＋甲酸钠体系为标准混合物溶液）,测定海水COD的相对标准偏差RSD为8．9％,回收率为90％～114％。     

一种催化降解有机废水制氢的资源化技术

提出了一种催化化学法降解有机废水制氢的资源化技术,特别是为生物难降解高毒性的有机废水的净化处理和制氢资源化利用提供了一条途径。在Raney Ni、Sn修饰的Raney Ni（Sn-Raney-Ni）或Pd／C等催化剂的作用下和比较温和的条件下,利用水相重整反应技术将废水中的有机物（如,苯酚、苯胺、硝基苯、四氢呋喃、甲苯、DMF和环己醇等）高选择性地降解为H2和CO2等无机分子。分别在连续固定床和间歇釜式反应器中的实验结果表明,在优化的反应条件下,有机废水的降解率和H2选择性均达到100％。Sn修饰的Raney Ni（Sn／Ni=0.06）和Pd／C催化剂比Raney Ni催化剂具有更好的降解有机废水制氢的性能。     

小茴香超临界CO_2萃取产物脂肪酸成分分析

通过脂肪酸的衍生化处理，再利用色谱（GC）和色谱一质谱（GC－MS）等分析手段，对小茴香超临界CO2萃取产物的脂肪酸成分进行了剖析，共鉴定出九种脂肪酸，其中，十八碳一烯酸、十八碳二烯酸和棕榈酸是其主要成分，分别占脂肪酸总量的75．12％、15．18％和5．34％．     

中国部分煤种二氯甲烷萃取液中极性和烃类有机物分布特性研究

利用高分辨气相色谱－低分辨质谱联用仪（HRGC／LRMS）检测原煤二氯甲烷萃取液中极性有机物和烃类有机物（脂肪烃和芳香烃）的浓度分布，研究了萃取液中这两类有机物和煤种、煤种成分（固定碳、挥发分、灰分、水分）之间的联系。研究发现萃取液中的有机物浓度和固定碳、挥发分关系密切；极性有机物分布较集中，主要为酯类和醇类；芳香烃以菲、二苯并蒽和苯并Bai为主，烟煤和贫煤多环芳烃含量和毒性当量（TEQ）相对较高，并发现煤的碳化程度越高，芳香化程度越大。本文的结果为将来进一步研究燃煤过程中有机污染物形成机理提供依据。     

烤鳗油的脂肪酸组成及其利用价值

用ＧＣ－ＭＳ法测定了烤鳗油脱腥前后的脂肪酸组成，并对其利用价值进行了评价。实验结果表明，经高温减压水蒸汽蒸馏脱腥处理后，烤鳗油中不饱和脂肪酸含量占其脂肪酸总量的７０％，二十碳五烯酸（ＥＰＡ）和二十二碳六烯酸（ＤＨＡ０含量分别达４．０１％和７．７３％。利用烤鳗油的结构特点，有可能开发出一系列特殊的保健品。     

废水中营养污染物的吸附及再利用

废水中营养污染物的吸附及再利用薛建军，王玲，田子华（南京航空航天大学材料科学与工程系南京２１００１６）（江苏省植物保护总站南京）关键词　废水，营养污染物，吸附，再利用本文介绍用固体废弃物──粉煤灰为主要原料经物理化学过程制成废水处理剂（其主要成分（％...     

大气有机物热脱附-全二维气相色谱-火焰离子化分析方法

全二维气相色谱（GC×GC）是20世纪90年代发展起来的具有高分辨率、高灵敏度、高峰容量等优势的分离技术,在我国将其用于大气挥发性有机物（VOCs）研究方面才刚刚起步.本文将GC-GC与氢火焰离子化检测器（FID）联用,构建了用于测量大气有机物的热脱附-全二维气相色谱-氢火焰离子化分析系统（TD-GC×GC-FID）.采用HP-5MS和HP-INNOWAX色谱柱,建立了C5-C15大气有机物分析方法,实现了一次分析过程同时分离非甲烷烃（NMHCs）、含氧挥发性有机物（OVOCs）和卤代烃等多种组分.利用标准物质和四级杆质谱（qMS）进行定性,外标法结合FID质量校正因子定量.目标物在GC-GC谱图中第一和第二维保留时间变化分别小于0.6s和0.02s,峰体积平均相对标准偏差为14.3%,其中烷烃和芳香烃为4.5%.标准曲线r2均值大于0.99,平均检出限为6.04ng,平均回收率为111%.利用该方法检测到2010年1月北京市区大气中400多种有机物（信噪比大于50）,鉴定了其中的103种物质,包括烷烃、烯烃、芳香烃、卤代烃、醛、酮、酯、醇和醚等.所测定有机物平均总浓度为51.3×10-9V/V,其中OVOCs约占51%,芳香烃约占30%,烷烃约占15%,卤代烃和烯烃分别占3%和1%.平均浓度最高的前3个组分是乙醇（9.84×10-9V/V）、丙酮（6.72×10-9V/V）和甲苯（3.48×10-9V/V）.     

有机膨润土的吸附性能研究

有机膨润土处理水中有机物的研究已有报道［1－4］，但尚无就改性所用的表面活性剂对有机膨润土吸附性能的影响及规律的系统研究，对有机膨润土与不同有机物间作用机理的报道也甚少［1］．本文用3种不同的阳离子表面活性剂改性膨润土，并从等温吸附线的特征和有机物的辛醇－水分配系数较系统地研究了有机膨润上对几种有机物的吸附性能和作用机理．1实验部分1．1材料原士为钠基膨润土，经测定其阳离子交换容量为7464meg／100g土；澳化十六烷基王甲铰（CTMAB）为分析纯，溪化十二烷基三甲铰（DTMAB，95％），演化十八烷基三甲按（OTMAB…     

Characterization and determination of organic compounds in the mutagenic XAD-2 extracts of drinking water.

Amberlite XAD-2 extracts, which exhibit mutagenicity in the Ames assays, of drinking water sampled each month during the period from April 1988 to March 1989 were studied in order to characterize and determine the organic pollutants. The major organic pollutants were phthalate ester plasticizers such as dibutyl and di(2-ethylhexyl) phthalate. Several polynuclear aromatic hydrocarbons (PAHs) and the organocholorine pesticide oxadiazon were also identified to be present at low concentrations. The XAD-extractable and chromatographable organic pollutants were found to be composed of PAHs with a mean concentration of 0.136 micrograms/l(ca. 10% of the total amount of organic compounds detected), phthalates with a mean value of 0.405 micrograms/l(ca. 30%) and other compounds with a mean value of 0.845 micrograms/l(ca. 60%). The concentrations and compositions of these organic pollutants were correlated with the effective rainfall content of the river and with the water temperature.     

气相色谱-质谱-自动质谱解卷积技术在沉积物和污泥中有机污染物非靶标筛查中的应用

以沉积物和污泥中非极性和弱极性有机污染物的非靶标筛查为目的,建立了一种超声波辅助提取-气相色谱-质谱结合自动解卷积技术的筛查方法。以二氯甲烷为溶剂超声波辅助提取样品3次,每次20 min,提取液经凝胶渗透色谱(GPC)和硅胶层析柱净化,再用3 g铜粉超声10 min除硫。前处理方法的重复性(RSD, n=5)为5.8%~14.9%。采用自动质谱解卷积软件(AMDIS)和标准谱库定性鉴别出所含的有机物。在两类样品中共鉴别出290种有机污染物,其中沉积物样品中190种,污泥样品中153种。鉴别出的污染物包括美国环境保护署(EPA)优先控制污染物、药物和除草剂等新型污染物、抗氧化剂、中间体、有机溶剂及化工原料等。该方法灵敏度高,重复性好,可用于复杂基质样品中有机污染物的非靶标筛查。     

Analysis of unknown organic pollutants in sewage by solid-phase extraction combined with gas chromatography-mass spectrometry

A rapid, simple, and reliable method of solid-phase extraction (SPE) combined with gas chromatography (GC)-mass spectrometry (MS) is developed for the analysis of a wide range of polarity of unknown organic pollutants in sewage. Wastewater samples are extracted by passing them through disposable C(18) cartridges, and the extracts are then analyzed by GC-MS. Different SPE parameters for ten organic compounds in the list of priority pollutants suggested by the China Environmental Protection Agency (EPA) are studied, and their breakthrough volumes are determined. Extraction recoveries for the tested compounds are greater than 60%, except the recovery of 1,2-dichloroethane is 48%. The relative standard deviations are less than 7.8% (n = 3). The developed approach is successfully applied for the identification of organic components in a sewage sample. Over 220 organic pollutants are identified, with 5 of these present in the list of priority pollutants suggested by the U.S. EPA and 4 from the list by the China EPA.     

高效液相色谱-串联质谱法同时测定水中13种有机污染物

以地表水环境质量标准严格控制的特定项目为依据,建立了直接进样-高效液相色谱-串联质谱同时测定水中13种化学性质差异较大的有机污染物的分析方法,这13种有机污染物为乐果、敌敌畏、敌百虫、对硫磷、甲基对硫磷、马拉硫磷、内吸磷、丙烯酰胺、苯胺、联苯胺、甲萘威、微囊藻毒素-LR、阿特拉津。水样经0.22 μm尼龙66滤膜过滤后,采用Kromasil 100-5 C18柱(150 mm×2.1 mm, 5 μm)分离,以甲醇-0.01%甲酸水溶液为流动相进行梯度洗脱,流速0.5 mL/min,柱温40 ℃,电喷雾正离子模式(ESI⁺)电离,多反应监测模式(MRM)进行检测,外标法定量。13种化合物的浓度与其峰面积在一定浓度范围内均呈现良好的线性关系(r≥0.9995),方法检出限为0.02~0.1 μg/L。测定低、中、高浓度的加标样品,13种化合物的相对标准偏差为0.5%~5.0%(n=6),实际样品加标平均回收率为81.2%~112%。此方法灵敏度高、干扰小、分析速度快,可适用于地表水、地下水中这13种有机污染物的同时分析。     

超临界流体萃取用于水中有机污染物的富集

研究了用固相吸附与超临界流体萃取相结合富集水中有机污染物的方法。考察了萃取压力,温度,改性剂种类及其浓度,收集溶剂种类,流体流速,平衡时间,流体用量８种因素对样品萃取脱附效果的影响及吸附剂的吸附线性范围,并对标准水样的富集回收率进行了测定。     

Determination of Trace Amounts of Organic Pollutants in the Yellow River by Capillary Column Gas Chromatography-Mass Spectrometry

Abstract

The trace organic pollutants in the Yellow River enriched by a solvent extraction method were pre-separated into four different fractions of fatty hydrocarbons, polycyclic aromatic hydrocarbons, polar compounds and organic acids and were analyzed by the use of combined capillary column gas chromatography-mass spectrometry. Using the combined techniques of relative retention value, mass spectra and mass chromatogram, more than 60 organic pollutants were identified, among which 16 fatty hydrocarbons and 6 polycyclic aromatic hydrocarbons which were quantitatively analyzed. The concentration range of fatty hydrocarbon was 5–800 ng/l, and that of polycyclic aromatic hydrocarbon was 0-90ng/l.     

成都地区雨水中有机污染物成份的研究

本文采用自行研制的雨水富集提取器吸附富集雨样中复杂有机物，不需预分离，直接用于ＧＣ和ＧＣ／ＭＳ分析。鉴定出１０２种有机物，并对ＢａＰ等２８种主要污染物作了定量测定。     

Estimation of contamination of atmosphere of Moscow in winter

To establish the priority pollutants in the atmosphere of Moscow in winter 8 snow samples were collected along the perimeter (109 km) of the Moscow Ring Road. Mass spectrometry was used as an analytical tool to identify individual organic compounds (gas chromatography/mass spectrometry) and the most environmentally relevant chemical elements (inductively coupled plasma with mass spectrometric detection). As a result several hundred organic compounds belonging to various classes, including representatives of the list of priority pollutants of the USA Environmental Protection Agency were identified. Their levels as well as the levels of chemical elements were quantified. The importance of accurate mass measurements for the efficient structural elucidation and reliability of quantitative measurements has been demonstrated. The data obtained allow estimating atmospheric pollution in Moscow in the period between December and March and proposing a list of priority pollutants for the atmosphere of Moscow.     

The potential of gas chromatography with microwave-induced plasma atomic emission detection (GC-MIP-AED) as a complementary analytical technique in environmental screening analysis of aqueous samples

With GC-MIP-AED as a complementary analytical technique to GC-MS, the reliable identification of many organic pollutants in water samples of the Nitra river has been made possible due to the additional information on the elemental composition of organic pollutants it provides. Some compounds, which have been identified by GC-MS in the scan mode after a MS-library search, can be confirmed by their element responses. Even where the identification of substances cannot be confirmed by their empirical formulas calculated by GC-MIP-AED due to insufficient peak intensities, integration problems or chromatographic interferences, it can be facilitated by the presence of one or more heteroatoms. Quantitative data of selected organic pollutants from GC-MIP-AED screening analysis after compound independent calibration can be obtained more easily than, and in good agreement with, quantitative results provided by target analysis (e.g. GC-MS in the SIM-mode). New self-developed macros are helpful tools for acquiring information on the elemental composition and concentration of organic pollutants analyzed by GC-MIP-AED. Received: 3 March 1997 / Revised: 11 June 1997 / Accepted: 11 June 1997     

The potential of gas chromatography with microwave-induced plasma atomic emission detection (GC-MIP-AED) as a complementary analytical technique in environmental screening analysis of aqueous samples

With GC-MIP-AED as a complementary analytical technique to GC-MS, the reliable identification of many organic pollutants in water samples of the Nitra river has been made possible due to the additional information on the elemental composition of organic pollutants it provides. Some compounds, which have been identified by GC-MS in the scan mode after a MS-library search, can be confirmed by their element responses. Even where the identification of substances cannot be confirmed by their empirical formulas calculated by GC-MIP-AED due to insufficient peak intensities, integration problems or chromatographic interferences, it can be facilitated by the presence of one or more heteroatoms. Quantitative data of selected organic pollutants from GC-MIP-AED screening analysis after compound independent calibration can be obtained more easily than, and in good agreement with, quantitative results provided by target analysis (e.g. GC-MS in the SIM-mode). New self-developed macros are helpful tools for acquiring information on the elemental composition and concentration of organic pollutants analyzed by GC-MIP-AED. Received: 3 March 1997 / Revised: 11 June 1997 / Accepted: 11 June 1997