分散液液微萃取气相色谱-质谱法测定水中15种硝基苯类化合物

建立了超声辅助基质分散液液微萃取（UA-DLLME）作为前处理联合气相色谱串联质谱（GC-MS）同时测定地下水和地表水中15种硝基苯类化合物的分析方法。萃取剂、分散剂、萃取温度、萃取时间和离子强度等影响因素采用Plackett-Burman设计,快速筛选出最显著影响因素,利用中心组合设计（CCD）简化实验步骤优化显著因素,结合响应曲面图最终确定最佳的萃取条件：5 mL水样在3%氯化钠条件下迅速加入40 μL四氯化碳（萃取剂）和0.5 mL乙腈（分散剂）,50 ℃下超声4 min,混合液4 000 r/min离心3 min。结果表明：15种硝基苯类化合物在50.0~1 000.0 μg/L的浓度范围内线性相关系数均大于0.995;采用超声辅助基质分散液液微萃取时,方法检出限（MDL）为0.018~0.039 μg/L;15种目标物的加标平均回收率为83.31%~99.08%,相对标准偏差均不高于5.0%（n=6）。     

柱前衍生-EI源串联四极杆气质联用测定地表水中的丙烯酰胺

建立了地表水中痕量丙烯酰胺的柱前衍生-EI源串联四极杆气质联用测定方法。丙烯酰胺的双键经溴化衍生成2,3-二溴丙酰胺,加入硫酸钠盐析,乙酸乙酯萃取,浓缩取1μl进样,由串联四极杆气相色谱质谱联用仪测定。通过MRM(150→70.0/107.0)多反应监测实现定性和外标法定量分析。与其他方法相比,该方法具有定性准确、灵敏度高的特点。方法检出限为0.03μg/L,线性范围在0.030~40μg/L;相关系数r=0.9998;六次测定值RSD在14.3%;回收率在89%~196%之间,结果满意。     

便携式顶空/气相色谱/质谱联用法快速测定水中苯系物

建立了以便携式顶空/气相色谱/质谱联用技术快速测定水中苯系物的方法,该方法适用于水中苯系物的应急监测。     

Analysis of α, β, γ-hexachlorocyclohexanes in water by novel activated carbon fiber-solid phase microextraction coupled with gas chromatography--mass spectrometry

A fast and simple method for determination of α, β,γ-hexachlorocyclohexanes (HCHs) in water using activated carbon fibersolid phase microextraction(ACF-SPME) were studied. Results showed the performance of adsorption and desorption of three HCHs on ACF were excellent. A wide linear range from 10 to 100 μg/L and detection limits of the ng/L level were obtained using ACF-SPME with GC-MS in selected ion monitoring(SIM) acquisition mode. The proposed method was also successfully applied for determination of three HCHs in tap water. Compared to commercial fibers, ACF showed some advantages such as better resistance to solvents, higher thermal stability, longer lifetime and lower cost. The data demonstrated that GC-MS with ACF-SPME is well suitable for the analysis of HCHs in water.     

PCDD/F in waste water discharges from flue gas scrubbers of waste incinerators and coal operated power plants

Scrubber water samples from different combustion plants and gypsum samples as obtained in the flue gas washing with lime water were analyzed for PCDD/F. Three of the investigated nine scrubber water samples showed PCDD/F contents between 0,4 and 11,5 ng I-TEq/1 where as in the 17 gypsum samples examined only in a few cases very low levels of HpCDD and OCDD could be detected.     

Organic compounds in the flue gas from a power station with circulating fluid bed combustion of coal

Numerous organic compounds have been analyzed by coupled gas chromatography-mass spectroscopy (GC-MS) in flue gas after fluid bed combustion of four coal species from South Africa, Poland, Spitsbergen and Ruhr area (Germany). Polynuclear aromatic hydrocarbons, aliphatic hydrocarbons, chlorinated, heterocyclic and nitro compounds as well as phthalate esters are detected.     

Antennal responses to floral scents in the butterflies <Emphasis Type="Italic">Inachis io</Emphasis>, <Emphasis Type="Italic">Aglais urticae</Emphasis> (Nymphalidae), and <Emphasis Type="Italic">Gonepteryx rhamni</Emphasis> (Pieridae)

Summary. To better understand the biological role of floral scents for butterflies, electrophysiological responses to floral scents were investigated using combined gas chromatography and electroantennographic detection (GC-EAD). The antennal responses of three butterfly species, Aglais urticae L. (Nymphalidae), Inachis io L. (Nymphalidae), and Gonepteryx rhamni L. (Pieridae) to floral scent compounds from both natural and synthetic mixtures were examined. Floral scents were collected from the butterfly nectar plants Cirsium arvense (L.) (Asteraceae), and Buddleja davidii Franchet cv. (Loganicaeae) with dynamic head-space methods on Tenax-GR and eluted with pentane. These eluates, composed of natural floral scent blends, represent an array of compounds in their natural state. In the GC-EAD analyses eleven compounds were identified from C. arvense with the benzenoid compound phenylacetaldehyde in highest abundance. Seventeen compounds were identified from B. davidii with the irregular terpene oxoisophorone in highest abundance. Thirty-nine synthetic floral scent compounds were mixed in pentane, in equal amounts; about 35 ng were allowed to reach the antennae. The butterflies showed antennal responses to most of the floral scent compounds from both natural and synthetic blends except to the highly volatile monoterpene alkenes. Certain benzenoid compounds such as phenylacetaldehyde, monoterpenes such as linalool, and irregular terpenes such as oxoisophorone, were emitted in relatively large amounts from C. arvense and B. davidii, and elicited the strongest antennal responses. These compounds also elicited strong antennal responses when present in the synthetic scent blends. Thus, the butterflies seem to have many and /or sensitive antennal receptors for these compounds, which points to their biological importance. Moreover, these compounds are exclusively of floral scent origin. For B. davidii, which depends highly on butterflies for pollination, the exclusive floral scent compounds emitted in high abundance could be the result of an adaptive pressure to attract butterflies. Received 2 Septemter 2001; accepted 9 September 2002.     

4-壬基酚在氯消毒过程中的氧化途径

利用固相萃取－GC－MS测定壬基酚（NP）及其在氯气消毒过程中产生的副产物。结果表明，NP容易和次氯酸发生反应，并检出了包括一氯壬基酚，二氯壬基酚，三氯苯酚在内的7种副产物。用量子化学模型探讨了NP和次氯酚的反应机理，NP和次氯酸的反应包括了苯环上的氯取代反应及壬基侧链的断裂反应。     

便携式GC-MS在室内空气VOC监测中的应用

本文采用苏码罐结合动态稀释权配置标准气体系列,建立了便携式GC-MS分析室内空气VOC的定量方法,并对便携式GC-MS和传统实验室GC-MS这两种检测方法进行对比研究。结果发现,便携式GC-MS和传统实验室GC-MS这两种检测方法所得结果并无显著差异。用便携式GC-MS对不同类型室内空气中VOC进行现场监测,操作简便、分析快速、灵敏度高,能够满足室内空气监测的要求。     

Residue levels of organochlorine pesticides in cattle meat and organs slaughtered in selected towns in West Shoa Zone,Ethiopia

Residue levels of organochlorine pesticides (OCP) in a total of 90 cattle samples comprising meat, liver and kidney collected from carcasses slaughtered in six towns in West Shoa Zone, Ethiopia, (Ambo, Guder, Ginchi, Gedo, Holeta and Tikur Inchini), have been determined. The pesticides were extracted by solid phase extraction (SPE) and quantification was carried out using gas chromatography-mass spectrometry (GC-MS). A good linearity (r² > 0.998) was found in the range 0.001–7.00 mg/kg for the samples studied. Most of the pesticides had recoveries in the range 81–99% and values of relative standard deviation (RSD) <7.2% for repeatability and reproducibility, showing good accuracy and precision of the method. The concentration level of the studied organochlorines followed the order: p, p’ dichloro-diphenyl-trichloroethane (DDT) > endosulfan>o,p′-DDT >lindane>dieldrin>endrin>aldrin>chlorothanolin while the order of contamination in the analyzed organs was liver > kidney > meat. Heat treatment of the meat, kidney and liver samples (boiling for 90 min.) produced an overall reduction of 62.2%, 44.5%, 37.7%, 29%, 31%, 34.3% and 30.8% in lindane, o, p′-DDT, endosulfan, p, p′-DDT, chlorothanolin, aldrin, dieldrin, and endrin, respectively. Although the residual contents of the organochlorines detected in all the contaminated samples analyzed from the six cities were below the respective maximal permissible levels set by international organizations, samples from Holeta town were more contaminated and may necessitate effective monitoring as bioaccumulation of these residues may pose health problems in human beings.