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The occurrence and temporal variation of selected priority substances and contaminants of emerging concerns, i.e., eleven perfluorinated compounds (PFCs, belonging to perfluorosulphonates, perfluorocarboxylic acids, and perfluorinated sulphonamides) have been investigated in composite surface water samples of the Danube River at the upstream and downstream locations from the discharge point of wastewater. Among the analyzed compounds, six PFCs (PFOA, PFOS, PFHxA, PFNA, PFDA and PFUnA) were quantified. Overall, the detection frequency for most quantified compounds was very high (>90 %), only PFDA and PFUnA were quantified with less frequency, 33 and 67 %, respectively. The highest quantified concentrations of PFOA and PFOS were 14.9 ng/L (average 12.1 ng/L) and 14.2 ng/L (average 6.11 ng/L), respectively. These ones together with PFHxA (average 10.0 ng/L) were quantified at the highest concentrations in comparison to the other investigated compounds. However, the determined levels of PFOS during investigated sampling period, for all samples analyzed, were always lower than the maximum allowable concentration set for inland river waters but always higher than the environmental quality standard threshold value-AA-EQS of 0.65 ng/L sets by the Directive of European Parliament. Moreover, the levels of PFOA were always several times lower than the set AA-EQS value.

The aim of this paper was to determine spatial variation of 6 indicator polychlorinated biphenyls (PCBs) and 18 organochlorine pesticides (OCPs) in street dust samples (n=49) collected during summer season from suburban/urban zones of Tianjin, China. Sample preparation was performed by using accelerated solvent extraction with simultaneous extraction and clean-up of PCBs and OCPs, while quantification was carried out using gas chromatography coupled with microelectro absorption detector and gas chromatography coupled with mass spectrometry. The total concentrations of studied PCBs varied from

In this paper, the most significant definitions of reactive power in single-phase and three-phase three-wire systems with non-sinusoidal voltages and currents are presented. Comparative analysis of these definitions has been performed. Fundamental principles on which these definitions rely are stated, and the application of these definitions to solving the problems of compensation is explained. Contrary to single-phase or three-phase symmetrical systems operating under sinusoidal conditions, reactive power compensation in systems operating under non-sinusoidal conditions does not result in maximal efficiency of electric energy delivery. Less efficiency in comparison to the theoretical maximum is being explained by the presence of harmonics and asymmetries in the system. Therefore, in the context of the reduction of losses during electric energy delivery to the load, the possibilities of nonactive power reduction should be contemplated instead of the possibilities of reactive power reduction.

The contents of major ions in bottled waters were analyzed by principal component (PCA) and hierarchical cluster (HCA) analysis in order to investigate if these techniques could provide the information necessary for classifications of the water brands marketed in Serbia. Data on the contents of Ca2+, Mg2+, Na+, K+, Cl-, SO4 2-, HCO3 - and total dissolved solids (TDS) of 33 bottled waters was used as the input data set. The waters were separated into three main clusters according to their levels of TDS, Na+ and HCO3 -; sub-clustering revealed a group of soft waters with the lowest total hardness. Based on the determined chemical parameters, the Serbian waters were further compared with available literature data on bottled waters from some other European countries. To the best of our knowledge, this is the first report applying chemometric classification of bottled waters from different European countries, thereby representing a unique attempt in contrast to previous studies reporting the results primarily on a country-to-country scale. The diverse character of Serbian bottled waters was demonstrated as well as the usefulness of PCA and HCA in the fast classification of the water brands based on their main chemical parameters. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. 172050]

The global environmental crisis, caused by the unreasonable behavior of human beings and their economic activities that affect nature and its resources, has created a basis for the development of new environmental paradigm, which emphasizes the intrinsic value of nature, the close connection between society and the environment and the importance of their mutual influence. Changing the view of the world becomes a necessary step in establishing the optimum of the inter­play between humans and the natural environment. Environmental knowledge is the most primary element of environmental awareness. The indispensable outcome of environmental awareness is ecological behavior that should be developed and encouraged. The formation of desirable behavior affect environmental objective and subjective factors. Objective factors are, for example, environmental conditions (degree of degradation of eco-system), socio-ecological infrastructure, the level of technological development. The subjective factors important for ecological behav­ior includes attitudes, expectations, political affiliation, personal and social values. For psychology, of particular importance are the values that support the behavior oriented towards environmental protection. This research examined the ecological value orientation and willingness to ecological involvement of students from the three groups of faculties: for mining and geology, for geography (environmental department), and faculties of social orientation (economic, law, philosophy . . . ). The results showed that the respondents have a well-developed environmental values that are a prerequisite for pro-environmental behavior and activities that leads to protection of the environment. Thus, the students were pretty much willing to engage in activities such as recycling various materials, use of public transportation and take other measures that contribute to a sustainable lifestyle.

Energy security and independence, increase and fluctuation of the oil price, fossil fuel resources depletion and global climate change are some of the greatest challanges facing societies today and in incoming decades. Sustainable economic and industrial growth of every country and the world in general requires safe and renewable resources of energy. It has been expected that re-arrangement of economies towards biofuels would mitigate at least partially problems arised from fossil fuel consumption and create more sustainable development. Of the renewable energy sources, bioenergy draws major and particular development endeavors, primarily due to the extensive availability of biomass, already-existence of biomass production technologies and infrastructure, and biomass being the sole feedstock for liquid fuels. The evolution of biofuels is classified into four generations (from 1st to 4th) in accordance to the feedstock origin; if the technologies of feedstock processing are taken into account, than there are two classes of biofuels - conventional and advanced. The conventional biofuels, also known as the 1st generation biofuels, are those produced currently in large quantities using well known, commercially-practiced technologies. The major feedstocks for these biofuels are cereals or oleaginous plants, used also in the food or feed production. Thus, viability of the 1st generation biofuels is questionable due to the conflict with food supply and high feedstocks’ cost. This limitation favoured the search for non-edible biomass for the production of the advanced biofuels. In a general and comparative way, this paper discusses about various definitions of biomass, classification of biofuels, and brief overview of the biomass conversion routes to liquid biofuels depending on the main constituents of the biomass. Liquid biofuels covered by this paper are those compatible with existing infrastructure for gasoline and diesel and ready to be used in mixture with them as „drop-in“ fuels: bioethanol, celullosic ethanol, biodiesel, renewable diesel and BtL diesel; their major advantages and drawbacks are compared. [Projekat Ministarstva nauke Republike Srbije, br. 172050]

The purpose of this work is to characterize biodiesel (i.e. methyl esters, MEs) produced from linoleic and oleic sunflower oils (LSO and OSO, respectively) by alkali transesterification with methanol and CaO as a heterogeneous catalyst under different reaction parameters. The parameters investigated were the methanol/oil molar ratio (4.5:1, 6:1, 7.5:1, 9:1 and 12:1) and the mass ratio of CaO to oil (2% and 3%). The physical and chemical properties of the feedstocks and MEs, like density at 15oC, kinematic viscosity at 40oC, acid value, iodine value, saponification value, cetane index, fatty acid (methyl ester) composition, were determined in order to investigate the effects of LSO and OSO properties and reaction parameters on the product characteristics, yields and purity. The properties of feedstock had decisive effect on the physical and chemical properties of MEs as majority of them did not differ significantly under studied reaction conditions. The MEs produced generally met the criteria required for commercial biodiesel; in fact, the only exception was in the case of iodine value of ME produced from LSO. The product yields only slightly changed with the applied conditions; the highest yield (99.22%) was obtained for ME-LSO produced at 6 mol% methanol to oil ratio, while the lowest one (93.20%) was for ME-OSO produced under the lowest methanol/oil molar ratio (4.5:1). The applied catalyst amounts had similar influence on the oil conversion to biodiesel. The yields of ME-LSOs were in general somewhat higher than those obtained for ME-OSOs under the same conditions, which was attributed to the influence of the respective feedstocks' acid value and viscosity.

The effects of the transesterification parameters on the yield and quality of the methyl esters (MEs) produced from waste frying oil (WFO) were investigated. A two-step alkali transesterification reaction followed by silica gel purification step was applied. The investigated reaction parameters were the methanol/oil molar ratio (6:1 and 9:1), the catalyst/oil weight ratio (1.0 and 1.5 mass %) and the type of catalyst (NaOH and KOH). The physical and chemical properties of the employed feedstock and the obtained biodiesel were determined in order to investigate the effects of both the properties of the WFO and the reaction parameters on the characteristics and yields of the product. It was found that the properties of the feedstock had a determinant effect on the physical and chemical properties of the MEs, as the majority of them did not differ significantly under the studied reaction parameters. However, the reaction parameters influenced the yields of the product. Higher yields were obtained with a 1.0 than with a 1.5 mass % catalyst to oil ratio. The increasing yield with decreasing catalyst/oil ratio was more pronounced with NaOH (9.15-14.35 %) than with KOH (2.84-6.45 %). When KOH was used as the catalyst, the yields were always higher (the mean yield was 94.86 %) in comparison to those obtained with NaOH (the mean was 84.28 %). Furthermore, the efficiency of KOH in conversion of WFO to purified MEs in comparison to NaOH was even more pronounced in the case of the higher methanol/oil ratio, i.e., for the 9:1 methanol/ oil ratio, the yield increase with KOH was about 2 times higher than the yield with NaOH, regardless of the applied catalyst/oil ratio.

The presence of polycyclic or polynuclear aromatic hydrocarbons (PAHs) were investigated in sugar-beet from a local sugar factory in the district of Vojvodina. The sugar-beet was cultivated on areas near roads with intensive traffic. The procedure for the preparation and determination of these compounds included saponification of the sample, several liquid–liquid extraction systems and a silica gel column clean-up. The purified sample solution was analysed by thin layer chromatography (TLC) on silica gel with cyclohexane as the developing solvent. Benzo(b)fluoranthene and benzo(a)anthracene and/or benzo(a)pyrene were detected at concentrations greater than the allowed limits in food.

A feed-forward artificial neural network (ANN) model was used to link molecular structures (boiling points, connectivity indices and molecular weights) and retention indices of polycyclic aromatic hydrocarbons (PAHs) in linear temperature- programmed gas chromatography. A randomly taken subset of PAH retention data reported by Lee et al. [Anal. Chem. 51 (1979) 768], containing retention index data for 30 PAHs, was used to make the ANN model. The prediction ability of the trained ANN was tested on unseen data for 18 PAHs from the same article, as well as on the retention data for 7 PAHs experimentally obtained in this work. In addition, two different data sets with known retention indices taken from the literature were analyzed by the same ANN model. It has been shown that the relative accuracy as the degree of agreement between the measured and the predicted retention indices in all testing sets, for most of the studied PAHs, were within the experimental error margins (+-3 %).

Endophytic fungi in symbiotic association with their host plant are well known to improve plant growth and reduce the adverse effects of both biotic and abiotic stresses. Therefore, fungal endophytes are beginning to receive increased attention in an effort to find growth-promoting strains that could be applied to enhance crop yield and quality. In our study, the plant growth-promoting activities of endophytic fungi isolated from various parts of Sophora flavescens (a medicinally important plant in Mongolia and China) have been revealed and investigated. Fungal isolates were identified using molecular taxonomical methods, while their plant growth-promoting abilities were evaluated in plate assays. Altogether, 15 strains were isolated, representing the genera Alternaria, Didymella , Fusarium and Xylogone . Five of the isolates possessed phosphate solubilization activities and twelve secreted siderophores, while all of them were able to produce indoleacetic acid (IAA) in the presence or absence of tryptophan. The endogenous and exogenous accumulation of IAA were also monitored in liquid cultures using the HPLC-MS/MS technique to refine the plate assay results. Furthermore, for the highest IAA producer fungi, the effects of their extracts were also examined in plant bioassays. In these tests, the primary root lengths of the model Arabidopsis thaliana were increased in several cases, while the biomasses were significantly lower than the control IAA treatment. Significant alterations have also been detected in the photosynthetic pigment (chlorophyll-a, -b and carotenoids) content due to the fungal extract treatments, but these changes did not show any specific trends.

Aflatoxins are mycotoxins that are produced by several species of filamentous fungi. In the European Union, the concentration limits for this group of mycotoxins in food and feed products are very low (on the order of parts per billion). Thus, relatively high amounts of these substances in their pure forms are required as reference standards. Chromatographic techniques based on solid stationary phases are generally used to purify these molecules; however, liquid-liquid chromatographic separations may be a promising alternative. Therefore, this study proposes a liquid-liquid chromatographic method for the separation of four aflatoxins and impurities. To optimise the method, numerous biphasic solvent systems (chloroform-, acetone- and acetic acid-based systems) were tested and evaluated in terms of their effectiveness at partitioning aflatoxins; the toluene/acetic acid/water (30:24:50, v/v/v/%) system was found to be the most efficient for application in centrifugal partition chromatographic instrument. Using liquid-liquid instrumental separation, the four aflatoxins, namely B 1 (400 mg), B 2 (34 mg), G 1 (817 mg) and G 2 (100 mg), were successfully isolated with 96.3%-98.2% purity from 4.5 L of Aspergillus parasiticus fermented material in a 250 mL centrifugal partition chromatography column. The identities and purities of the purified components were confirmed, and the performance parameters of each separation step and the whole procedure was determined. The developed method could be effectively used to purify aflatoxins for analytical applications.

In the present study, endophytic fungi have been isolated from various parts of the medicinal herb Hypericum perforatum (St. John's Wort), which is known as a source of medically important metabolites. The isolated strains were cultured in liquid media and their ability to synthesize hypericin, the secondary metabolite of the host and its suspected precursor, emodin was tested analyzing the extracts of the fermentation broth and the mycelia. The HPLC-UV analysis of the chloroform/methanol extracts of the mycelia revealed that three isolates were able to produce emodin (SZMC 23771, 19.9 ng/mg; SZMC 23772, 20.8 ng/mg; SZMC 23769, 427.9 ng/mg) and one of them also could synthesize hypericin (SZMC 23769, 320.4 ng/mg). These results were also confirmed via UHPLC-HRMS technique both in full scan and MS/MS mode. The strains producing only emodin belong to the section Alternata of the genus Alternaria, while the isolate producing both metabolites was identified as Epicoccum nigrum. The mycelial extracts of E. nigrum and the Alternaria sp. SZMC 23772 showed higher inhibitory activities in the antimicrobial tests against the six selected bacteria compared to the hypericin and emodin standards in the applied concentration (100 μg/mL), while in case of the Alternaria sp. SZMC 23771 lower inhibition activities were observed on Staphylococcus aureus and Streptomyces albus than the pure compounds., Competing Interests: The authors have declared that no competing interests exist.

This is the first investigation that identified seasonal occurrence, distribution and sources of 16 polycyclic aromatic hydrocarbons (PAHs) in 60 street dust samples collected within urban zone of Novi Sad, the second largest city in Serbia. The obtained results were further used for comprehensive assessment of carcinogenic risk of Serbian inhabitants exposed to PAHs present in street dust by the incremental lifetime cancer risk method. The total level of 16 PAHs ranged between 35 μg kg -1 and 2422 μg kg -1 in samples taken in summer and between 35 μg kg -1 and 587 μg kg -1 in samples taken in winter. In both seasons, 4-ring PAHs were the most dominant compounds and high molecular weight (HMW) PAHs had similar contribution (55% in summer and 65% in winter). The highest content was determined for fluoranthene (Fly) in both seasons (597 μg kg -1 in winter, 301 μg kg -1 in summer). The PAHs source apportionment was analyzed by principal component analysis (PCA) and diagnostic ratios, and combustion of petroleum seemed to be the main sources of the PAHs in street dust. The cancer risk level for children and adult were comparable for dermal contact and by ingestion, and ranged from 10 -6 to 10 -4 indicating a potential risk. Additionally, the total incremental life time cancer risk (ILCR) was assessed for children and adult population taking into account three possible exposure routs and the median total cancer risk was ˃10 -5 , with 7% of the samples having the risk ˃10 -4 that should be considered of high concern with potential health problem. These results are the first of this kind for the whole Serbia and the Western Balkan region and can be considered as the base line for future research., (Copyright © 2018 Elsevier B.V. All rights reserved.)

This study aims to compare three extraction techniques of four sequential element extraction steps from soil and sediment samples that were taken from the location of the Pančevo petrochemical industry (Serbia). Elements were extracted using three different techniques: conventional, microwave and ultrasound extraction. A novel procedure - sum of the ranking differences (SRD) - was able to rank the techniques and elements, to see whether this method is a suitable tool to reveal the similarities and dissimilarities in element extraction techniques, provided that a proper ranking reference is available. The concentrations of the following elements Al, Ba, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, Pb, Si, Sn, Sr, V and Zn were determined through ICP OES. The different efficiencies and recovery values of element concentrations using each of the three extraction techniques were examined by the CRM BCR-701. By using SRD, we obtained a better separation between the different extraction techniques and steps when we rank their differences among the samples while lower separation was obtained according to analysed elements. Appling this method for ordering the elements could be useful for three purposes: (i) to find possible associations among the elements; (ii) to find possible elements that have outlier concentrations or (iii) detect differences in geochemical origin or behaviour of elements. Cross-validation of the SRD values in combination with cluster and principal component analysis revealed the same groups of extraction steps and techniques., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

An online ultra-high-performance-liquid chromatography-triple quadrupole tandem mass spectrometry (UHPLC-MS/MS) method for detection and quantification of natural and synthetic estrogens and their conjugates in aqueous matrices was developed. Target compounds include the natural estrogen estradiol (E2) and its main metabolites estrone (E1) and estriol (E3), the synthetic estrogens ethinylestradiol (EE2) and diethylstilbestrol (DES) and their conjugates estrone 3-sulfate (E1-3S), estriol 3-sulfate (E3-3S), estradiol 17-glucuronide (E2-17G), estrone 3-glucuronide (E1-3G), and estriol 16-glucuronide (E3-16G). After pH adjustment, sample filtration and addition of internal standards (IS), water samples (5 mL) were preconcentrated on a Hypersil GOLD aQ column after which chromatographic separation was achieved on a Kinetex C18 column using methanol and water as a mobile phase. The experimental parameters, such as sample loading flow rate, elution time, the percentage of organic solvent in the aqueous-organic eluent mixture, pH, and volume of analyzed samples, were optimized in detail. The benefits of the method compared to previously published methods include minimum sample manipulation, lower detection limits, reduced total analysis time, and overall increased method accuracy and precision. Method detection limits (MDLs) are in subnanogram per liter, complying with the requirements of the EC Decision 2015/495 (Watch list) for hormones listed therein. Applicability of the developed method was confirmed by analysis of river and raw wastewater samples taken directly from urban sewerage systems before being discharged into the river. Graphical abstract Sheme of online SPE-UHPLC-MS/MS system.

A reliable, fast and simple method using UHPLC-MS/MS was developed for the determination of aflatoxins B 1 (AFB1), G 1 (AFG1), B 2 (AFB2) and G 2 (AFG2), ochratoxin A (OTA), deoxynivalenol (DON), zearalenone (ZEA), HT-2 toxin and T-2 toxin in crude extracts of biscuits with fruit filling, cookies, dried fruits and fruit jams. The method was successfully demonstrated on 39 samples of biscuits with fruit filling, 34 cookies, 14 dried fruits and 10 fruit jams. The mycotoxins detected in biscuits samples were ZEA, OTA, T-2 and AFB1 with an average concentrations of positive samples of 2.64, 4.10, 8.13 and 1.32 µg kg -1 , respectively; while the mycotoxins detected in jam samples were AFB1, OTA, T-2 and AFB2 with an average concentrations of positive samples of 2.00, 17.7, 4.37 and 1.15 µg kg -1 , respectively. The results showed that the majority of samples were in compliance with relevant regulations. However in eight samples of biscuits and three samples of fig jam the contents of OTA were higher than the existing OTA limits. The combined dietary exposure of selected mycotoxins was estimated for the first time for children, adolescents and adults. The estimated combined dietary exposures were all lower than the proposed value assumed to predict a possible risk scenario.

About 10 heavy elements were determined in 90 samples of baby food collected from Spanish and Serbian market. The results indicated that iron, manganese and copper were most frequently detected. Tin was the predominant toxic element in both Spanish and Serbian samples, with occurrence frequencies of 12.5% and 10.0%, respectively. Element intake for Spanish and Serbian infants were estimated and compared with the recommended reference values, for the majority of elements being lower than one. However, iron and manganese intake through consumption of infant/follow-on formulas were assessed to be higher than the respective daily intakes. Particular attention should be paid to the exposure of infants who consume porridges made of vegetables and fish or chicken, because they may ingest certain elements, particularly arsenic and lead, at levels that exceed the reference toxicological values. Principal component analysis (PCA) was applied to classify and distinguish the different types of baby food.

Acid esterification of sludge palm oil, having 50 mas.% free fatty acids, i.e., 50 g of dominant free fatty acid per 100 g of oil, was investigated with the objective of determining conditions for the efficient reduction of free fatty acids. The influences of sulphuric acid dosage and molar ratio of methanol to oil were studied, with the final intention to obtain feedstock with a free fatty acids content acceptable for biodiesel production by alkali-transesterification. Esterification was performed using different molar ratios of methanol to oil (3:1, 6:1 and 9:1) and varying the amount of H2SO4 catalyst (0.92 mas.%, 1.84 mas.% and 4.60 mas.%). Under the applied conditions, the sulphuric acid dosage of 4.60 mas.% resulted in the satisfactory decrease of the feedstock's free fatty acids for 6:1 and 9:1 molar ratios of methanol to oil. Thus, taking into account the economic reasoning, it can be concluded that approximately 5 mas.% of H2SO4 with 6:1 molar ratio of methanol to oily feedstock, might be regarded as the dosage necessary for satisfactory pretreatment of the feedstock to be further subjected to the alkaline transesterification. Finally, the effort to consolidate the information on acid esterification available in literature was made, contributing to knowledge on sustainable biodiesel production using the low-grade and low-cost sources., (© The Author(s) 2015.)

Commercial preparations of Cordyceps sinensis, Ganoderma lucidum and Coprinus comatus mushroom marketed as healthy food supplements in Serbia were analyzed by atomic absorption spectrometry with a graphite furnace (GFAAS) for their element content. Antioxidant activity potential and total phenolics of the same mushrooms were determined. The element content of mushroom samples was in the range of 0.130-0.360 mg kg(-1) for lead (Pb), <0.03-0.46 mg kg(-1) for arsenic (As), 0.09-0.39 mg kg(-1) for cadmium (Cd), 98.14-989.18 mg kg(-1) for iron (Fe), 0.10-101.32 mg kg(-1) for nickel (Ni), 5.06-26.50 mg kg(-1) for copper (Cu), 0.20-0.70 mg kg(-1) for cobalt (Co), 1.74-136.33 mg kg(-1) for chromium (Cr) and 2.19-21.54 mg kg(-1) for manganese (Mn). In the tests for measuring the antioxidant activity, the methanolic extract of C. sinensis showed the best properties. The same was seen for the analysis of selected phenolic compounds; C. sinensis was found to have the highest content. Commercial preparations of C. sinensis and C. comatus can be considered to be safe and suitable food supplements included in well-balanced diets.

This study assessed the levels of 21 perfluoroalkyl substances (PFASs) in 283 food items (38 from Brazil, 35 from Saudi Arabia, 174 from Spain and 36 from Serbia) among the most widely consumed foodstuffs in these geographical areas. These countries were chosen as representatives of the diet in South America, Western Asia, Mediterranean countries and South-Eastern Europe. The analysis of foodstuffs was carried out by turbulent flow chromatography (TFC) combined with liquid chromatography with triple quadrupole mass spectrometry (LC-QqQ-MS) using electrospray ionization (ESI) in negative mode. The analytical method was validated for the analysis of different foodstuff classes (cereals, fish, fruit, milk, ready-to-eat foods, oil and meat). The analytical parameters of the method fulfill the requirements specified in the Commission Recommendation 2010/161/EU. Recovery rates were in the range between 70% and 120%. For all the selected matrices, the method limits of detection (MLOD) and the method limits of quantification (MLOQ) were in the range of 5 to 650 pg/g and 17 to 2000 pg/g, respectively. In general trends, the concentrations of PFASs were in the pg/g or pg/mL levels. The more frequently detected compounds were perfluorooctane sulfonic acid (PFOS), perfluorooctanoic acid (PFOA) and perfluorobutanoic acid (PFBA). The prevalence of the eight-carbon chain compounds in biota indicates the high stability and bioaccumulation potential of these compounds. But, at the same time, the high frequency of the shorter chain compounds is also an indication of the use of replacement compounds in the new fluorinated materials. When comparing the compounds profile and their relative abundances in the samples from diverse origin, differences were identified. However, in absolute amounts of total PFASs no large differences were found between the studied countries. Fish and seafood were identified as the major PFASs contributors to the diet in all the countries. The total sum of PFASs in fresh fish and seafood was in the range from the MLOQ to 28ng/g ww. According to the FAO-WHO diets composition, the daily intake (DI) of PFASs was calculated for various age and gender groups in the different diets. The total PFASs food intake was estimated to be between 2300 and 3800 ng /person per day for the different diets. Finally, the risk intake (RI) was calculated for selected relevant compounds. The results have indicated that by far in no case the tolerable daily intake (TDI) (150, 1500, 50,000, 1,000,000, 150, 1500 ng/kg body weight, for perfluorohexanesulfonate (PFHxS), fluorotelomer alcohol (FTOH), perfluorobutanesulfonic acid (PFBS), perfluorobutanoic acid (PFBA), PFOS and PFOA, respectively) was exceeded., (Copyright © 2014 Elsevier Inc. All rights reserved.)

Laccase-producing fungi were isolated from air, using selective media with a chromogenic substrate to indicate enzyme activity. The best laccase producer strain proved to be a Leptosphaerulina chartarum isolate. Laccase production was investigated in the presence of various inducers in different cultivation conditions. The extracellular laccase was purified for further investigations. SDS-PAGE showed that this laccase is a monomeric protein of 38 kDa molecular weight. The enzyme is active in the pH-range of 3.5-6, with an optimum at pH 3.8. It is active in the 10-60 °C temperature range, with an optimum at 40 °C. After 20 min incubation at temperatures above 70 °C the enzyme lost its activity. Degradation of seven aniline and phenol compounds (2,4-dichlorophenol; 2-methyl-4-chlorophenol; 3-chloroaniline; 4-chloroaniline; 2,6-dimethylaniline; 3,4-dichloroaniline and 3-chloro-4-methylaniline) was investigated, with or without guaiacol (2-methoxyphenol) as mediator molecule. Addition of a mediator to the system significantly increased the degradation levels. These results confirmed that the isolated laccase is able to convert these harmful xenobiotics at in vitro conditions.

The aim of the work was to study the occurrence of pharmaceuticals in waste, surface, underground, and drinking water samples collected in Serbia. A multi-residue method for the analysis of 81 pharmaceutical drugs from different therapeutic classes in the various types of water was applied. Twenty-five composite water samples were prepared using solid-phase extraction and the presence of 81 pharmaceutical compounds in the extracts was analyzed by ultra-high performance liquid chromatography coupled to mass spectrometry with hybrid triple quadrupole-linear ion trap (UPLC-QqLIT-MS/MS). Forty seven compounds of 81 drugs were found in four different types of analyzed water. The highest concentrations of ibuprofen of 20.1 μg L(-1), 10,11-epoxycarbamazepine of 16.2 μg L(-1), 2-hydroxycarbamazepine of 15.9 μg L(-1) and acetaminophen of 15.7 μg L(-1) were found in municipal waste water sample. Results revealed the presence of salicylic acid in 41.67% of water samples, carbamazepine in 36.11%, propranolol and irbesartan in 30.56%. The obtained results were discussed in relation to the relevant data available in literature. This is the first attempt to assess the occurrence of these 81 pharmaceutical residues in water samples in Serbia., (© 2013.)

Sum of ranking differences (SRD) was applied for comparing multianalyte results obtained by several analytical methods used in one or in different laboratories, i.e., for ranking the overall performances of the methods (or laboratories) in simultaneous determination of the same set of analytes. The data sets for testing of the SRD applicability contained the results reported during one of the proficiency tests (PTs) organized by EU Reference Laboratory for Polycyclic Aromatic Hydrocarbons (EU-RL-PAH). In this way, the SRD was also tested as a discriminant method alternative to existing average performance scores used to compare mutlianalyte PT results. SRD should be used along with the z scores--the most commonly used PT performance statistics. SRD was further developed to handle the same rankings (ties) among laboratories. Two benchmark concentration series were selected as reference: (a) the assigned PAH concentrations (determined precisely beforehand by the EU-RL-PAH) and (b) the averages of all individual PAH concentrations determined by each laboratory. Ranking relative to the assigned values and also to the average (or median) values pointed to the laboratories with the most extreme results, as well as revealed groups of laboratories with similar overall performances. SRD reveals differences between methods or laboratories even if classical test(s) cannot. The ranking was validated using comparison of ranks by random numbers (a randomization test) and using seven folds cross-validation, which highlighted the similarities among the (methods used in) laboratories. Principal component analysis and hierarchical cluster analysis justified the findings based on SRD ranking/grouping. If the PAH-concentrations are row-scaled, (i.e., z scores are analyzed as input for ranking) SRD can still be used for checking the normality of errors. Moreover, cross-validation of SRD on z scores groups the laboratories similarly. The SRD technique is general in nature, i.e., it can be applied to any experimental problem in which multianalyte results obtained either by several analytical procedures, analysts, instruments, or laboratories need to be compared.