Primary biodegradation of veterinary antibiotics in aerobic and anaerobic surface water simulation systems

The primary aerobic and anaerobic biodegradability at intermediate concentrations (50-5000 microg/l) of the antibiotics olaquindox (OLA), metronidazole (MET), tylosin (TYL) and oxytetracycline (OTC) was studied in a simple shake flask system simulating the conditions in surface waters. The purpose of the study was to provide rate data for primary biodegradation in the scenario where antibiotics pollute surface waters as a result of run-off from arable land. The source of antibiotics may be application of manure as fertilizer or excreta of grazing animals. Assuming first-order degradation kinetics, ranges of half-lives for aerobic degradation of the four antibiotics studied were 4-8 days (OLA), 9.5-40 days (TYL), 14-104 days (MET) and 42-46 days (OTC). OLA and OTC were degraded with no initial lag phase whereas lag phases from 2 to 34 days (MET) and 31 to 40 days (TYL) were observed for other substances. The biodegradation behaviour was influenced by neither the concentrations of antibiotics nor the time of the year and location for sampling of surface water. Addition of 1 g/l of sediment or 3 mg/l of activated sludge from wastewater treatment increased the biodegradation potential which is believed to be the result of increased bacterial concentration in the test solution. Biodegradation was significantly slower in tests conducted in absence of oxygen. Assessments of the toxic properties of antibiotics by studying the influence on the biodegradation rates of 14C-aniline at different concentrations of antibiotics showed that no tests were conducted at toxic concentrations.     

Nanotechnology for improved production of algal biofuels: a review

Environmental Chemistry Letters - Fossil fuel depletion and carbon dioxide emissions are calling for carbon neutral energies such as algal biofuels, yet actual production of agal biofuels is...     

Noninvasive monitoring of DNAPL migration through a saturated porous medium using electrical impedance tomography

Electrical impedance tomography (EIT) was used to monitor the movement of a fluorinated hydrocarbon dense nonaqueous phase liquid (DNAPL) through a saturated porous medium within a laboratory column. Impedance measurements were made using a horizontal plane of 12 electrodes positioned at regular intervals around the centre of the column. A 2D inversion algorithm, which incorporated the cylindrical geometry of the column, was used to reconstruct resistivity and phase images from the measured data. Differential time-lapse images of DNAPL movement past the plane of electrodes were generated by the cell-by-cell subtraction of resistivity and phase baseline models from those associated with the DNAPL release stage of the experiment.The DNAPL pulse was clearly delineated as resistive anomalies in the differential time-lapse resistivity images. The spatial extent of the resistive anomalies indicated that in addition to vertical migration, some lateral spreading of the DNAPL had occurred. Residual contamination could be detected after quasi-static conditions were reestablished. Residual DNAPL saturation was estimated from the resistivity model data by applying Archie's second equation.Despite significant measured phase changes due to DNAPL contamination, the differential phase images revealed only weak anomalies associated with DNAPL flow; these anomalies could be seen only in the initial stages of the experiment during peak flow through the plane of electrodes.     

Sonication and grinding pre-treatments on <Emphasis Type="Italic">Gelidium amansii</Emphasis> seaweed for the extraction and characterization of Agarose

Various pretreatments methods including sonication and grinding were performed on red seaweed Gelidium amansii for the subsequent extraction of agarose. The agarose products are usually extracted from agar powder products from seaweeds. In this study, the agarose was extracted using a direct polyethylene glycol (PEG) method without the need to first process the agar from seaweed. The agar extract was frozen then thawed and mixed directly with PEG solution to precipitate the agarose. The quality of agarose obtained was evaluated through physico-chemical properties analysis which includes spectral technique (FTIR), melting and boiling point, gel strength and sulfate content. These properties were compared with a non-pretreated sample and it was found that the addition of pretreatment steps improved the quality of agarose but gave a slightly lower yield. The gel strength of pretreated samples was much higher and the sulfate content was lower compared to non-pretreated samples. The best pretreatment method was sonication which gave gel strength of 742 g cm^-2 and sulfate content of 0.63%. The extraction of agarose can be further improved with the use of different neutralizing agents. Pretreating the seaweed shows potential in improving the quality of agarose from seaweed and can be applied for future extraction of the agarose.

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Stability of Tylosin A in manure containing test systems determined by high performance liquid chromatography

Tylosin is a widely used antibiotic for the treatment of infections in swine. Tylosin consists of a mixture of Tylosin A, Tylosin B, Tylosin C and Tylosin D. All components contribute to the potency of tylosin but Tylosin A is by far the major component (usually about 90% and not less than 80%). A fast, robust and easily performed HPLC method has been developed for determination of Tylosin A in the presence of tylosin residues; Tylosin B, Tylosin C and Tylosin D in manure containing incubation media. The separation was performed using a YMC-Pack ODS-AQ column (250 x 4.6 mm i.d., 5 microns particle size) operated at 35 degrees C. The mobile phase consisted of 2.25% (w/v) sodium perchlorate pH 2.5-acetonitrile (60:40 v/v). Detection was performed by measuring the UV absorption at a wavelength of 290 nm. Calibration curves of tylosin made in the incubation medium containing 6.4% manure were linear in the range from 0.375 to 128.0 mg/l (R2 = 0.999). The limit of quantitation (at the RSD 20% level) for Tylosin A was found to be 0.4 mg/l in incubation media containing 6.4% manure. The recovery of Tylosin A was in the range from 100% to 108% depending on the concentration of manure. The reproducibility was good as the relative standard deviation (n = 4) in each matrix tested was in the range from 0.7 to 1.9 at the 25 mg/l level. The stability of Tylosin A was studied under methanogenic conditions and the half-life was found to be less than two days. Studies under aerobic conditions showed that the degradation rate was found to increase with increasing concentrations of manure particles in the incubation medium. It is, however, not clear whether the decrease in the concentration of Tylosin A is caused by sorption, abiotic or biotic chemical degradation. The major degradation product of Tylosin A in methanogenic as well as aerobic incubation media has a UV-spectrum and a retention time corresponding to Tylosin B. Furthermore, Tylosin D is believed to be a minor degradation product.     

Ionic liquids for the inhibition of gas hydrates. A review

The formation of gas hydrates is a major issue during the operation of oil and gas pipelines, because gas hydrates cause plugging, thereby disrupting the normal oil and gas flows. A solution is to inject gas hydrate inhibitors such as ionic liquids. Contrary to classical inhibitors, ionic liquids act both as thermodynamic inhibitors and hydrate inhibitors, and as anti-agglomerates. Imidazolium-based ionic liquids have been found efficient for the inhibition of CO₂ and CH₄ hydrates. For CO₂ gas hydrates, N-ethyl-N-methylmorpholinium bromide showed an average depression temperature of 1.72 K at 10 wt% concentration. The induction time of 1-ethyl-3-methyl imidazolium bromide is 36.3 h for CO₂ hydrates at 1 wt% concentration. For CH₄ hydrates, 1-ethyl-3-methyl-imidazolium chloride showed average depression temperature of 4.80 K at 40 wt%. For mixed gas hydrates of CO₂ and CH₄, only quaternary ammonium salts have been studied. Tetramethyl ammonium hydroxide shifted the hydrate liquid vapour equilibrium to 1.56 K at 10 wt%, while tetrabutylammonium hydroxide showed an induction time of 0.74 h at 1 wt% concentration.

     

Determination of the distribution coefficient (log Kd) of oxytetracycline,tylosin A,olaquindox and metronidazole in manure

Olaquindox (log Kow = -2.3) and metronidazole (log Kow = -0.1) both have low tendencies to sorp to particles in manure. This corresponds with the negative log Kow values of these antibiotics. Tylosin (log Kow = 1.63) and oxytetracycline (log Kow = -1.12) sorp relatively strongly to the manure particles and have log Kd values between 1.5 and 2.0. The tendency to bind to manure was ranked after increasing binding as follows: metronidazole < olaquindox < tylosin A and oxytetracycline. This order of ranking is consistent with results of sorption in soil. Our experiments illustrate that for some antibacterial agents estimation of the partitioning coefficients, Kd, cannot be made from Kow and f(oc) alone. Sorption of oxytetracycline to manure is much higher than expected from the negative log Kow value of the compound. It is believed that sorption of oxytetracycline to manure is influenced by ionic binding to divalent metal ions as such Mg2+ and Ca2+ as well as other charged compounds in the matrix. Binding of oxytetracycline to soil is stronger than the binding to manure. This is most likely due to the strong mineral related metal complexes formed between soil, metal ion and oxytetracycline. These complexes are not known to exist in manure. The relatively strong sorption of tylosin A to manure corresponds with data found for soil sorption of tylosin. Tylosin has a log Kow value of 2.5, thus it is not surprising that this drug binds strongly to manure.     

Production of hydrogen and value-added carbon materials by catalytic methane decomposition: a review

Environmental Chemistry Letters - Dihydrogen (H2), commonly named “hydrogen”, is attracting research interest due to potential applications in fuel cells, vehicles, pharmaceuticals and...