对油品仓储区大气中NMHC特征的监测分析

采用气相色谱-质谱联用方法对油品仓储区大气中的非甲烷总烃(NMHC)进行分类定量测定,通过对仓储区内不同点位NMHC浓度的差异和各自日变化规律进行分析,可以认为烷烃和烯烃有较高的浓度水平,其中烯烃含量最高。文章还对油品仓储区域大气中NMHC的排放特征进行了探讨。     

顶空固相微萃取-气相色谱-串联质谱法测定水中2,4,6-三氯酚

建立了顶空固相微萃取-气相色谱-串联质谱法(HS-SPME-GC-MS-MS)测定水中2,4,6-三氯酚的方法。优化条件下,在1. 00～50. 0μg/L质量浓度范围内线性响应良好(r~2=0. 999 1);检出限0. 224μg/L,测定下限0. 896μg/L;加标样相对标准偏差(RSD)为4. 15%～6. 24%;加标回收率为81. 0%～115%;单个样品检测总时间40 min。该方法萃取与气相色谱-串联质谱分析在线一步完成,操作简便、灵敏度高、抗干扰性强,适用于地表水、生活饮用水、工业废水等水体中2,4,6-三氯酚的检测。     

离子色谱法应用于杭州地表水中有机酸及无机阴离子分布研究

建立了离子色谱-抑制电导法同时检测杭州市地表水中的有机酸及无机阴离子,并对地表水中有机酸及无机阴离子的含量进行探讨.该方法的重现性(RSD)为0.15％ ～4.92％,相关系数r2为0.9990 ～ 0.9999,加标回收率为84.36％～111.05％,最低检出限为0.003～0.028 mg/L.利用该建立的方法,...     

加速溶剂萃取-超高效液相色谱（UPLC）测定土壤中苯并（a）芘

本文优化了加速溶剂萃取-超高效液相色谱测定土壤中苯并（a）芘的方法。样品经加速溶剂提取,逐级减压浓缩,0.25um滤膜过滤净化,超高效液相色谱（UPLC）测定。结果表明,标准溶液苯并（a）芘含量在3.125～lOOug／L范围内,苯并（a）芘的线性呈良好的线性关系,相关系数为0.9999,该方法的检出限和测定下限分别为0.015μg/kg和0.060μg/kg。将该方法用于4个地区土壤样品的测定,苯并（a）芘含量在0.04～6.26ug／kg之间,空白加标回收率为75.2％～96.4％之间,各项指控指标符合检测要求。     

The determination of partition coefficients of organic compounds in technical products and waste waters for the estimation of their bioaccumulation potential using reversed phase thin layer chromatography

Reversed phase thin layer chromatography (RPTLC) has been investigated for the estimation of octanol/water partition coefficients (P), an important parameter for the prediction of the environmental behaviour of organic chemicals. A strong correlation between P derived from the traditional octanol/water system and RPTLC has been established over five orders of magnitude. RPTLC data are likewise correlated to results obtained by high performance chromatography (HPLC). Due to the low costs, simplicity and separation power RPTLC is especially suited for the investigation and screening of mixtures of compounds before more complicated tests are involved.

Results from a round robin test on the determination of partition coefficients by HPLC, RPTLC and the batch method indicate the simplicity and accuracy of the RPTLC technique. Applications of the RPTLC‐technique on technical products and industrial waste waters are described.     

Metallothionein induction in mice by CCL4: Hepatic Zn‐status and distribution of administered Cd∗

Induction of metallothionein (MT), Zn status and the subcellular distribution of administered Cd were studied in liver after single administration of CC1₄ to mice. Hepatic MT was increased up to 153±16 μMT/g liver 18 h after injection of 2ml CCl₄/kg body weight. The observed decrease in Zn bound to cytosolic high molecular weight proteins from 25.5 ± 0.6 to 19.8±1.1 resp. 19.0 ± 1.7 μgZn/g and the increase in MT bound Zn from 4.0±0.5 to 9.5 ± 1.1 resp. 10.9±1.1 μgZn/g compensate each other.

Zn content of whole liver and hepatic cytosol remained unchanged. Hepatic subcellular distribution of 4 mg Cd/kg body weight, administered 2 h prior termination was also influenced by CC1₄. Cd bound to high molecular weight proteins decreased from 10.0±1.0 to 7.2±1.6 resp. 3.7 ± 2.6 μg Cd/g and Cd bound to MT increased from 12.5 ± 1.4 to 18.0 ± 3.8 resp. 23.1± 6.4 μgCd/g. Cd content of both, whole liver and cytosol was not significantly different from control. The induction of MT has been suggested to be beneficial due to its role in the sequestration of toxic metals. The depletion of Zn from cytosolic high molecular weight proteins however might adversively influence essential physiological processes.     

Dissipation kinetics of novaluron in tomato,an arid ecosystem pilot study

Novaluron, a newly introduced insecticide, is used for control of a number of field pests. However, information regarding novaluron residues and dissipation profile is limited. In this study, dissipation and residual levels of novaluron in tomato under open field conditions were investigated using high performance liquid chromatography equipped with diode array detector (HPLC-DAD) with quick, easy, cheape, effective, rugged (QuEChERS) method. The method was validated using blank samples spiked at three levels and results showed that recoveries ranged from 93% to 99%. Novaluron residues tend to dissipate following first-order rate kinetics with half-life of 2.08 days. Data demonstrated that the use of novaluron at recommended doses would not pose any hazards to consumers. The present results aid to establish the safe use of this pesticide on tomatoes, and possibly on other crops in Egypt.     

Distribution,removal and chemical forms of heavy metals in polluted rice seed

In this paper, the distribution, removal and binding forms of heavy metals in polluted seeds of rice were studied using the methods of histochemistry and biochemistry. The results indicate that the distribution of heavy metals in rice grains was very uneven. The heavy metals in rice grains chiefly exist in association with the parts of high protein. Separation of proteins by Sephadex chromatography and subsequent analysis by atomic absorption spectroscopy revealed that Cd, Pb and As were mainly bound to protein of 54.5 and 5.50 kD molecular weights. During the rice processing, the concentrations of heavy metals in the edible rice decrease greatly, for some heavy metals in these parts of chaff, coarse rice bran and fine rice bran were removed.     

Determination of pesticides in apples,grapes and apple juice from a Kosovo market by gradient liquid chromatography with tandem mass spectrometry

Apple, grape, and apple juice were analyzed for pesticides using a multireaction mode (MRM) method in samples taken from a Kosovo market. With this method it was possible to analyze about 100 pesticides in the ESI mode. In these samples some types of pesticides were found, but most of them did not exceed the maximum tolerance levels. In apple samples, six pesticides were detected but only three of them were in sufficient quantitites. Dimethoat was below the limit, while acephate and imazalil exceeded the limit. In grape and apple juice samples, all of pesticides which were found did not exceed the maximum tolerable limits.     

在线柱浓缩-液相色谱法测定水体中痕量敌草快和百草枯

采用在线柱浓缩-超快速液相色谱联用技术测定水体中痕量百草枯和敌草快.水样无需样品前处理,过滤后即可进样.采用固相萃取小柱富集待测物,以色谱梯度泵完成样品的净化后,利用阀切换技术将待测物反冲至分析柱进行分离,以二极管阵列检测器定量.方法在1.0—20.0μg.L-1范围内线性良好,百草枯和敌草快的线性相关系数分别为0.9997和0.9989.百草枯和敌草快的检出限(S/N=3)分别为0.10、0.12μg.L-1,加标回收率在96.0%—98.0%之间.用所建立的方法测定了水中痕量的百草枯与敌草快的含量,结果令人满意.