1,359 research outputs found

    Performance evaluation of powdered activated carbon for removing 28 types of antibiotics from water

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    © 2016 Elsevier Ltd. Currently, the occurrence and fate of antibiotics in the aquatic environment has become a very serious problem in that they can potentially and irreversibly damage the ecosystem and human health. For this reason, interest has increased in developing strategies to remove antibiotics from water. This study evaluated the performance of powdered activated carbon (PAC) in removing from water 6 representative groups of 28 antibiotics, namely Tetracyclines (TCs), Macrolides (MCs), Chloramphenicols (CPs), Penicillins (PNs), Sulfonamides (SAs) and Quinolones (QNs). Results indicate that PAC demonstrated superior adsorption capacity for all selected antibiotics. The removal efficiency was up to 99.9% in deionized water and 99.6% in surface water at the optimum conditions with PAC dosage of 20 mg/L and contact time of 120 min. According to the Freundlich model's adsorption isotherm, the values of n varied among these antibiotics and most were less than 1, suggesting that the adsorption of antibiotics onto PAC was nonlinear. Adsorption of antibiotics followed well the pseudo-second-order kinetic model (R2 = 0.99). Analysis using the Weber-Morris model revealed that the intra-particle diffusion was not the only rate-controlling step. Overall, the findings in this study confirm that PAC is a feasible and viable option for removing antibiotics from water in terms of water quality improvement and urgent antibiotics pollution control. Further research is essential on the following subjects: (i) removing more types of antibiotics by PAC; (ii) the adsorption process; and (iii) the mechanism of the competitive adsorption existing between natural organic matters (NOMs) and antibiotics

    Occurrence, fate and health risk assessment of 10 common antibiotics in two drinking water plants with different treatment processes

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    © 2019 Elsevier B.V. The occurrence of antibiotics in drinking water has become a serious problem worldwide as they are a potential and real threat to human health. In this study, the variability of 10 typical antibiotics in two drinking water plants was investigated in two seasons (n = 12). The total concentrations of target antibiotics in raw water were significantly higher in winter than in summer, which may be attributed to the more frequent occurrence of colds and respiratory diseases as well as less rainfall in winter. The efficiency in removing the antibiotics varied from −46.5% to 45.1% in water plant A (WP-A) using a conventional process and 40.3% to 70.3% in water plant B (WP-B) with an advanced treatment process. Results indicated that the antibiotics in WP-A were mainly removed via the coagulation process. However in WP-B, the ultraviolet + chlorination process played a key role in antibiotics removal, followed by the pre-ozone + coagulation process. According to the human health risk assessment, it was suggested that the risk of drinking water was significantly higher than that of skin contact. However, the risk of carcinogenesis and non-carcinogenesis caused by antibiotics was at an acceptable level

    New Terms for the Compact Form of Electroweak Chiral Lagrangian

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    The compact form of the electroweak chiral Lagrangian is a reformulation of its original form and is expressed in terms of chiral rotated electroweak gauge fields, which is crucial for relating the information of underlying theories to the coefficients of the low-energy effective Lagrangian. However the compact form obtained in previous works is not complete. In this letter we add several new chiral invariant terms to it and discuss the contributions of these terms to the original electroweak chiral Lagrangian.Comment: 3 pages, references adde

    Behavior of nitrogen removal in an aerobic sponge based moving bed biofilm reactor

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    © 2017 Elsevier Ltd This study aims to investigate the behavior of nitrogen removal in an aerobic sponge based moving bed biofilm reactor by evaluating nitrification and denitrification rates of sponge biocarriers from three aerobic moving bed biofilm reactors (MBBRs) with filling ratios of 10% (R-10), 20% (R-20) and 30% (R-30). Results showed that the highest removal efficiencies of total nitrogen in three reactors were 84.5% (R-10), 93.6% (R-20) and 95.3% (R-30). Correspondingly, simultaneous nitrification and denitrification rate (SND) was 90.9%, 97.6% and 100%, respectively. Although R-20 had the highest attached-growth biomass (AGB) per gram of sponge compared to the other two reactors, R-30 showed the maximum ammonium oxidation rate (AOR) (2.1826 ± 0.0717 mg NH4+-N/g AGB/h) and denitrification rate (DNR) (5.0852 ± 0.0891 mg NO3−-N/g AGB/h), followed by R-20 and R-10. These results indicated AOR, DNR and AGB were affected by the filling ratio under the same operation mode

    Photoexcitation of bulk polarons in rutile TiOâ‚‚

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    The excitation of surface-localized polaronic states has recently been discussed as an additional photocatalytic channel to band gap excitation for rutile Ti O 2 . A contribution from photoexcitation of bulk polarons could, in principle, provide a greater contribution because of their higher number and their protection from oxidation. However, determining such a contribution to the photoyield is challenging and has not been achieved thus far. Here we use two photon photoemission spectroscopy measurements to separate bulk and surface polaron photoexcitation. We find that bulk polarons are less bound by 0.2 eV compared with polarons at the surface, consistent with our results of hybrid density functional theory calculations. Because the excited state is also shifted to higher energy, bulk polarons have the same photoexcitation resonance energy as at the surface (3.6 eV) with a threshold at 3.1 eV. This is degenerate with the band gap, suggesting that bulk polarons could also provide an additional contribution to the photoyield

    Food waste based biochars for ammonia nitrogen removal from aqueous solutions

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    © 2019 Elsevier Ltd Biochar derived from waste has been increasingly considered as a potential green adsorbent due to its significant ability and affordable production costs. This study prepared and evaluated 7 types of food waste-based biochars (FWBBs) (including meat and bone, starchy staples, leafy stemmed vegetables, nut husks, fruit pericarp, bean dreg and tea leaves). The impacts of raw materials, pyrolysis temperatures (300, 400, 500, 600 and 700 °C), and residence time (2 h and 4 h) on the removal of ammonia nitrogen at different ammonia nitrogen concentrations (5, 10, 20, 50, 100, 150 mg/L) were investigated. The batch equilibrium and kinetic experiments confirmed that a FWBB dosage of 3 g/L at 25 °C could remove up to 92.67% ammonia nitrogen. The Langmuir isotherm model had the best fit to equilibrium experimental data with a maximum adsorption capacity of 7.174 mg/g at 25 °C. The pseudo-second order kinetic model well describes the ammonia nitrogen adsorption

    Characterization and sulfonamide antibiotics adsorption capacity of spent coffee grounds based biochar and hydrochar.

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    A large amount of spent coffee grounds is produced as a processing waste each year during making the coffee beverage. Sulfonamide antibiotics (SAs) are frequently detected in the environment and cause pollution problems. In this study, biochar (BC) and hydrochar (HC) were derived from spent coffee grounds through pyrolysis and hydrothermal carbonization, respectively. Their characteristics and sulfonamide antibiotics adsorption were investigated and compared with reference to adsorption capacity, adsorption isotherm and kinetics. Results showed BC possessed more carbonization and less oxygen-containing functional groups than HC when checked by Elemental Analysis, X-ray diffraction, X-ray photoelectron spectrometry and Fourier transform infrared. These groups affected the adsorption of sulfonamide antibiotics and adsorption mechanism. The maximum adsorption capacities of BC for sulfadiazine (SDZ) and sulfamethoxazole (SMX) were 121.5 μg/g and 130.1 μg/g at 25 °C with the initial antibiotic concentration of 500 μg/L, respectively. Meanwhile the maximum adsorption capacities of HC were 82.2 μg/g and 85.7 μg/g, respectively. Moreover, the adsorption mechanism for SAs adsorbed onto BC may be dominated by π-π electron donor-acceptor interactions, yet the SAs adsorption to HC may be attributed to hydrogen bonds. Further analysis of the adsorption isotherms and kinetics, found that physical and chemical interactions were involved in the SAs adsorption onto BC and HC. Overall, results suggested that: firstly, pyrolysis was an effective thermochemical conversion of spent coffee grounds; and secondly, BC was the more promising adsorbent for removing sulfonamide antibiotics

    Sparse Exploratory Factor Analysis

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    Sparse principal component analysis is a very active research area in the last decade. It produces component loadings with many zero entries which facilitates their interpretation and helps avoid redundant variables. The classic factor analysis is another popular dimension reduction technique which shares similar interpretation problems and could greatly benefit from sparse solutions. Unfortunately, there are very few works considering sparse versions of the classic factor analysis. Our goal is to contribute further in this direction. We revisit the most popular procedures for exploratory factor analysis, maximum likelihood and least squares. Sparse factor loadings are obtained for them by, first, adopting a special reparameterization and, second, by introducing additional [Formula: see text]-norm penalties into the standard factor analysis problems. As a result, we propose sparse versions of the major factor analysis procedures. We illustrate the developed algorithms on well-known psychometric problems. Our sparse solutions are critically compared to ones obtained by other existing methods

    New Fe-based superconductors: properties relevant for applications

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    Less than two years after the discovery of high temperature superconductivity in oxypnictide LaFeAs(O,F) several families of superconductors based on Fe layers (1111, 122, 11, 111) are available. They share several characteristics with cuprate superconductors that compromise easy applications, such as the layered structure, the small coherence length, and unconventional pairing, On the other hand the Fe-based superconductors have metallic parent compounds, and their electronic anisotropy is generally smaller and does not strongly depend on the level of doping, the supposed order parameter symmetry is s wave, thus in principle not so detrimental to current transmission across grain boundaries. From the application point of view, the main efforts are still devoted to investigate the superconducting properties, to distinguish intrinsic from extrinsic behaviours and to compare the different families in order to identify which one is the fittest for the quest for better and more practical superconductors. The 1111 family shows the highest Tc, huge but also the most anisotropic upper critical field and in-field, fan-shaped resistive transitions reminiscent of those of cuprates, while the 122 family is much less anisotropic with sharper resistive transitions as in low temperature superconductors, but with about half the Tc of the 1111 compounds. An overview of the main superconducting properties relevant to applications will be presented. Upper critical field, electronic anisotropy parameter, intragranular and intergranular critical current density will be discussed and compared, where possible, across the Fe-based superconductor families

    The inner core hemispheric boundary near 180°W

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    The inner core (IC) east–west hemispheric dichotomy is widely recognized, but the reported position of the hemispheric boundary varies among studies due to uneven sampling coverage and the data analyzed. This study investigates the sharpness of the western hemispheric boundary (WHB) near 180°W by analyzing differential time residuals of PKiKP–PKPdf and PKP(bc–df) for PKPdf phases that sample 155°E–130°W in various azimuthal directions. Using PKiKP–PKPdf observations, the WHB is located at 175°E–180°W in the southern hemisphere, based mainly on the lateral isotropy–anisotropy transition. However, based on the lateral isotropic velocity contrast and this isotropy–anisotropy transition between the two hemispheres, its location is 170–160°W in the northern hemisphere. These findings indicate that the WHB is sharp and exhibits a latitudinal dependence with a 10°–20° kink, as well as 1.75% anisotropy in the uppermost IC across the 180–155°W range of the western hemisphere. As suggested by PKP(bc–df), the WHB could remain at 160°W at depth. The isotropic velocity contrast near the WHB (160°W) between the eastern and western hemispheres is lower than previous estimates using PKPdf phases sampling the bulk part of each hemisphere
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