垃圾焚烧炉烟气中二噁英的测定

采用标准采样分析方法,对垃圾焚烧炉烟气样品中的二喃英进行取样、提纯和HRGC/HRMS分析,对样品中4～8个氯取代的二噁英取得定量结果。      

Estimate of sea loading by pollutants originating from the littoral counties in the Republic of Croatia

The paper reviews the data of 10 yr of following up sewage (waste water) inflows of anthropological origin into the sea from all the coastal settlements in Croatia. In particular, we report the sea loading by biochemical oxygen demand (BOD₅), expressed by the inhabitant equivalent (I.E.), for seven littoral counties. We estimated the loading of a coastal sea area for each county separately. The objective was to avoid any over- or underestimation of amounts and significance of sewage inflows into the seawater. For this purpose, a precisely determined sea volume up to the 10 m isobath has been chosen. Because of the inadequate treatment of wastewater, the total loading of that maritime territory expressed in terms of i.e. was found to be 26% higher than expected from the actual number of inhabitants. However, daily input represents only 12‰ of the considered volume of the sea. Recipient spent only 0.7% of the disposable oxygen quantity in the sea.     

Ultrasound-assisted emulsification/microextraction based on solidification of trace amounts of thallium prior to graphite furnace atomic absorption spectrometry determination

In the present work, determination of ultratrace amounts of thallium in water samples was performed by ultrasound-assisted emulsification microextraction based on solidification of a floating organic drop as sample preparation method prior to furnace atomic absorption spectrometry. 1-(2-Pyridylazo)-2-naphthol was used as chelating agent. The factors influencing the complex formation and extraction, such as pH of the aqueous solution, the type and the volume of extraction solvent, the volume of chelating agent solution, and the extraction time were investigated. Under optimized conditions, the enrichment factor was 200. The calibration graph was linear from 0.2 to 10.0 μg L^?1 with a correlation coefficient of 0.9966, the detection limit was 0.03 μg L^?1 and reproducibility was ±3.3% (C = 5.0 μg L^?1, n = 8). The method was successfully applied for the determination of thallium in water samples.     

Environmental impact assessment for aquatic ecosystems of industrial effluents†

A system of environmental impact assessment of industrial effluents is presented and discussed. Environmental assessment consists of three phases, hazard assessment, risk determination, and societary evaluation. It is regarded an integrated study of natural sciences, i.e. ecochemicology (chemical fate), ecotoxicology (toxical effects), and ecoepidemiology (biological damages); and social sciences, e.g. geography, sociology, and economy. And the outcome should be the basis of political decision making. Hazard assessment may be divided into a subphase of hazard identification from a base set of scientific information on the industrial effluent, and a second subphase of hazard analysis at a more elevated level of scientific information akin to the procedures suggested elsewhere for single chemicals. Methods of hazard assessment are laboratory experiments, e.g. chemical analysis, degradation and bioaccumulation studies, acute and chronic toxicity assessments, physical modelling, etc. Risk determination may then be conducted by extrapolation of the obtained results from laboratory to field, i.e. by risk estimation to the receiving waters, using methods of hydraulic modelling, biological surveillance, etc. Risk‐benefit evaluation is conducted in the society evaluation phase by balancing environmental consequences against the society value of the production. The outcome is determined by the interaction between hazard‐makers (industry), risk‐takers (administrators), guardians (regulators), and assessors (scientists) in risk management, the crank of environmental assessment.     

Detection of metallothionein in the intestinal mucosa and brain with 109cadmium∗

Metallothionein (MT) has a great capacity of binding metal ions showing an interesting connection with metal toxicology, as a biochemical marker for environmental metal pollution.

To normal male Wistar rats (200±10 g) and other groups with ferropenic anemia, are administered 1 mg Cd/Kg/day, during 6 days, and MT labelled with the administration 2 h before sacrifice of 3 μCi ¹⁰⁹CdCl₂, also through intragastric catheter. The MT concentration in the intestinal mucosa is expressed in μg MT/g fresh tissue, being for control rats 1.4 ± 0.5; for rats administered with 6 doses of Cd 2.5 ± 0.6 (P<0.05); with ferropenic anemia 4.3±0.7 (P<0.001), and for anemic rats treated with 6 doses Cd 12 + 0,3 (P<0.001) μg MT/g fresh tissue respectively. PAGE 15% T, 2% C_Bis show for intestinal mucosa 2 MT peaks and for brain 3 MT peaks. Anemia induce MT accumulation and increases cadmium incorporation, being anemic subjects eligibles to be submitted first to control and detoxication than the rest of the population, and also MT should be studied as biochemical marker of the pollution.     

Trace analysis of airborne toluene diisocyanate as a pentafluorobenzyl derivative by gas chromatography with electron capture detection

Trace analysis of airborne toluene diisocyanate (TDI) vapor was accomplished by measuring the derivative using gas chromatography with electron‐capture detector after collecting gas samples with a microimpinger containing 2 ml toluene, 1 μl pentafluorobenzyl alcohol, and 1 μl triethylamine. The sampling efficiency was determined to be 99.4% for short‐term exposure level of TDI and the 2,4‐ and 2,6‐isomers of TDI were well separated. The derivative was identified to be a new compound with a molecular weight of 570 by mass spectrometry in fast atomic bombardment mode and nuclear magnetic resonance spectrometry. This method is convenient and can be applied in the field where airborne TDI is in vapor form.     

加速溶剂萃取-气质联用同步测定土壤中17组分多溴二苯醚

建立了加速溶剂萃取-气相色谱-质谱法(ASE-GC/MS)同步定量分析土壤中17组分多溴二苯醚(PBDEs)的方法.选用正己烷和二氯甲烷混合液(体积比为1∶1)为萃取剂,样品经加速溶剂萃取后由氧化铝复合硅胶柱净化,气相色谱-负化学源-质谱法测定.结果表明:在32 min内,包括高溴代二苯醚在内的17组分PBDEs同族体在同一较短毛细管色谱柱上得到了较好的分离.该方法中BDE209的回收率为80.80%,其余BDE的回收率为86.39%～103.19%;BDE209的方法检出限为198.33 pg/g,其他16组分PBDEs同族体的方法检出限为0.85～114.33 pg/g.该方法检测土壤中多组分PBDEs的灵敏度高、重现性和回收率良好,可用于土壤样品PBDEs的分析.      

微波Sol-Gel制备TiO2的研究及其对活性艳红X-3B的降解

采用微波Sol-Gel法在石英表面制备了负载型TiO2光催化剂,通过紫外吸收光谱和X衍射分析表征了TiO2溶胶的变化过程及锐钛型TiO2的生成。以活性艳红X-3B为模拟污染物进行光催化降解,探讨了微波功率、反应温度和反应时间对微波Sol-Gel法制备TiO2光催化活性的影响。由因素试验确定了最佳工艺条件:微波功率400W,反应温度90℃,反应时间2min。在此条件下制备的TiO2催化剂对活性艳红X-3B溶液进行光催化降解,反应30 min的脱色率达93%,TOC去除率为55%。采用中空纤维膜三相液相微萃取-毛细管电泳(HF-LLLME-CE)联用技术对降解生成的小分子有机物进行了测定。     

食醋中总酸、总酯含量的连续测定

提出了利用连续分析技术定量地测定食醋中总酸、总酯的含量。操作简捷、快速、准确、所获的结果与常规法基本一致,此法对食醋的质量控制具有一定的现实意义。     

五管发酵测定粪大肠菌群的研究

通过实验摸索出粪大肠菌群的一种五管发酵法。该方法检测下限为9个/L,适用于地表水和废水中粪大肠菌群的测定。