Comparison of different modifications on QuEChERS sample preparation method for PAHs determination in black, green, red and white tea

The aim of this work was the evaluation of QuEChERS extraction method for polycyclic aromatic hydrocarbon (PAH) determination in various types of tea. In the experiment, different kinds of extraction solvents, sorbents and a final method of sample preparation were compared. The final extracts were analysed by gas chromatography-selected ion monitoring-mass spectrometry. The results suggest that acetonitrile extraction, clean up with SAX and final liquid–liquid extraction was the best combination giving the most purified extracts and acceptable compound recoveries for different types of teas. In the study of real samples, compounds belonging to light PAHs were mostly detected, and heavy polycyclic aromatic hydrocarbons, including benzo[a]pyrene, were not identified in any of samples.     

锑矿区土壤重金属污染及优势植物对重金属的富集特征

通过野外调查采样,分析了冷水江锑矿区4个采样点土壤和优势植物中重金属含量,以及矿区生长的5种优势植物对Sb、As、Cd、Pb、Cu和Zn的的吸收与富集能力及其富集特性。结果表明,矿区土壤中6种重金属元素的平均含量均超出湖南省土壤背景值和全国土壤背景值,土壤受Sb污染最严重,其次是Cd、As的污染。5种优势植物淡竹叶、苎麻、芒草、狗尾草和白背叶体内Sb、As的含量都超过正常范围,具有修复矿区土壤Sb、As污染的潜力。其中苎麻对Sb的富集系数和转运系数均大于1,满足Sb超富集植物的基本特征,可作为生态恢复的先锋植物;芒草对Cd的富集系数和转运系数都大于1,对重金属有较强的耐性,作为重金属污染的修复植物具有较好的应用前景。     

Direct N2O emission from agricultural soils in Poland between 1960 and 2009

Nitrogen fertilization (N) is commonly known as a main source of direct nitrous oxide (N₂O) emission from agricultural soils. An area of 38 % of the total land surface of Poland was covered by agricultural soils in 2009. In this paper, we aimed at analyzing data regarding the land exploitation for 13 selected subareas of Poland between 1960 and 2009. Seven out of the 13 subareas studied are located in the West (area A), and six subareas are located in southeast of Poland (area B). The total area covered by large farms (>20 ha) differed largely, between area A (10.6 %) and area B (0.9 %) in 2009. Both areas varied in terms of the amount of fertilizers used annually, average crop yield and crop structure. Average direct emissions of N₂O from agricultural soils were 1.66 ± 0.09 kg N₂O–N ha^?1 a^?1 for area A, 1.39 ± 0.07 kg N₂O–N ha^?1 a^?1 for area B and 1.46 ± 0.07 kg N₂O–N ha^?1 a^?1 for the whole country between 1960 and 2009.     

Removal possibilities of colloidal chromium (III) oxide from water using polyacrylic acid

The lack of water is the most serious threat to humanity that leads to more efficient water and sewage treatment. Currently, many scientists are looking for new coagulants, flocculants and physicochemical methods allowing for sufficient removal of pollutants from water. The presence of various types of pigments, including chromium (III) oxide, poses the major problem. Even small amounts of these substances inhibit life processes in water. In this paper, the stability of Cr₂O₃ suspension in the absence and the presence of polyacrylic acid (PAA) was determined. To explain the changes in the system stability, the adsorption and electrokinetic measurements were performed. The chromium (III) oxide suspension not containing PAA is the most stable at pH?=?3. Under these conditions, each positively charged solid particle is surrounded by a negatively charged diffusion layer which protects from particle collision and aggregates formation (electrostatic stabilization). In turn, the Cr₂O₃ suspension containing the PAA is most unstable also at pH?=?3. In this case, the polymer causes destabilization of the colloidal suspension, which results from charge neutralization of solid particles by adsorbed PAA.     

Study on the determination of PCDDs/Fs and HCB in exhaust gas

The subject of this study was to develop a method of simultaneous determination of PCDDs/PCDFs and HCB in exhaust gases from industrial installations. Sampling to determine PCDDs/PCDFs was conducted using the method described in PN-EN 1948-1: 2006, where the sorption material is polyurethane foam (PUF). In order to simultaneously collect PCDDs/PCDFs and HCB and to avoid sorbent bed breakthrough, it was necessary to apply an additional polyurethane sorption layer. Twenty-seven samples of exhaust gases from various cement plants and 40 samples of exhaust gases from hospital and industrial waste incineration plants collected in 2009/2010 in the entire territory of Poland were examined. The average content of PCDDs/Fs in samples from cement plants amounted to 0.076 ng I-TEQ N m(-3) (range of 0.002-0.62 ng I-TEQ N m(-3)), while the average content of HCB amounted to 10 ng N m(-3) (range of 0.98-60.5 ng N m(-3)). In the case of samples collected from waste incineration plants, the average concentration of PCDDs/Fs was 0.39 ng I-TEQN m(-3) (range of 0.002-5.68 ng I-TEQ N m(-3)). In the case of HCB, the average concentration was 238 ng N m(-3) (range of 3.21-2500 ng N m(-3)). Also, the interdependence of the concentration of PCDDs/PCDFs and HCB was determined in the analysed samples, with the ranges of low and high content of PCDDs/PCDFs being examined separately. In all cases, the determined values of the r correlation coefficient were within the range of 0.7-1.0, which indicates a good correlation between the concentrations of PCDDs/PCDFs and HCB.