The effect of cyclic aerobic-anoxic conditions on biodegradation of benzoate.

The response of a mixed microbial culture to cyclic aerobic and anoxic (denitrifying) conditions was studied in a chemostat with a 48-hour hydraulic residence time receiving a feed containing benzoate and pyruvate. When the cyclic conditions were 3-hour aerobic and 9-hour anoxic, the bacteria-degraded benzoate aerobically via the catechol 2,3-dioxygenase (C23DO) pathway. The quantity of C23DO remained constant throughout the anoxic period but decreased during the initial portion of the aerobic period before returning to the level present in the anoxic period. Anoxic biodegradation of benzoate was via benzoyl-CoA reductase, which remained constant regardless of the redox condition. The aerobic benzoate uptake capability (AeBUC) of the culture increased during the aerobic period but decreased during the anoxic period. The anoxic benzoate uptake capability (AnBUC) exhibited the opposite response. When the cycle was 6-hour aerobic and 6-hour anoxic, aerobic biodegradation of benzoate proceeded via the protocatechuate 4,5-dioxygenase (P45DO) pathway. The P45DO activity decreased early in the aerobic period, but then increased to the level present during the anoxic period. The level of benzoyl-CoA reductase was constant throughout the cycle. Furthermore, AeBUC and AnBUC responded in much the same way as in the 3/9-hour chemostat. During a 9-hour aerobic and 3-hour anoxic cycle, the culture synthesized both P45DO and C23DO, with the former having significantly higher activity. Unlike the other two cycles, AeBUC changed little during the aerobic period, although AnBUC decreased. The culture was well-adapted to the cyclic conditions as evidenced by the lack of accumulation of either substrate during any cycle tested. This suggests that cyclic aerobic-anoxic processes can be used in industrial wastewater-treatment facilities receiving significant quantities of simple aromatic compounds like benzoate. However, the results showed that the kinetics of benzoate degradation were different under aerobic and anoxic conditions, a situation that must be considered when modeling cyclic bioreactors receiving aromatic compounds.     

Simultaneous Removal of Cationic and Anionic Dyes from Binary Solutions Using Carboxymethyl Chitosan Based IPN Type Resin

Journal of Polymers and the Environment - In this study, a novel bead form IPN type resin comprising poly (2-Dimethylaminoethyl) methacrylate and carboxymethyl chitosan networks with a high dye...     

Higher number of microplastics in tumoral colon tissues from patients with colorectal adenocarcinoma

Environmental Chemistry Letters - Microplastics have been detected in marine and terrestrial ecosystems, yet the toxic effects of microplastics on living organisms are poorly known. In particular,...     

Impacts of COD and DCP loading rates on biological treatment of 2,4-dichlorophenol (DCP) containing wastewater in a perforated tubes biofilm reactor

Biofilm processes offer considerable advantages for biological treatment of chlorophenol containing wastewaters since such industrial effluents are difficult to treat by conventional activated sludge processes. A rotating perforated tubes biofilm reactor (RTBR) was developed and used for treatment of 2,4-dichlorophenol (DCP) containing synthetic wastewater. Effects of COD and DCP loading rates on COD, DCP and toxicity removals were investigated. Percent COD removal decreased and effluent COD increased with increasing COD and DCP loading rates due to toxic effects of high DCP content in the feed. DCP and toxicity removals showed similar trends. As the DCP loading rate increased the effluent DCP content increased yielding high toxicity levels in the effluent. COD and DCP loading rates should be below 90gCODm(-2)d(-1) and 2.8gDCPm(-2)d(-1) in order to obtain more than 90% DCP and toxicity removals. However, DCP loading rates lower than 1gDCPm(-2)d(-1) are required to obtain more than 90% COD removal. Empirical equations were developed to estimate percent COD, DCP and toxicity removals as functions of COD and DCP loading rates. The coefficients of the empirical equations were determined by using the experimental data. Empirical model predictions for percent COD, DCP and toxicity removals were in good agreement with the experimental data.     

Vertical and horizontal distribution,source identification,ecological and toxic risk assessment of heavy metals in sediments of Lake Aygır,Kars, Turkey

Surface and core sediment samples were collected from Lake Ayg?r, Turkey, to determine heavy metal distribution, probable sources and potential ecological and toxic risks for the lake. Heavy metals, total sulfur, total phosphate, total organic carbon, chlorophyll degradation products, and CaCO₃ content were established. The enrichment factor, PLI, potential ecological risk index, and toxic risk index were calculated. Zn was determined to have the highest accumulation in surface sediment, followed by Cr, Pb, and Cd, respectively. Cd was the only element that exceeded the critical value of 40 and posed a moderate potential ecological risk. According to TRI, no ecotoxic risk was found. It is thought that local fossil fuel consumption is responsible for the accumulation of heavy metals since there is a lack of urbanization, industrialization, and agricultural activities around the lake.     

Determination of heavy metals in lower Sakarya river sediments using a BCR-sequential extraction procedure

A BCR-sequential extraction procedure for the determination of extractable heavy metals was applied to sediments of various rivers and lakes. There are many rivers basins in Turkey. Sakarya River Basin is one of the most important basins, which consists of three parts: Upper, Middle and Lower Sakarya River Basins. In this study, the Lower Sakarya River was selected as the study area for sediments. The samples were collected monthly from 10 pre-determined stations through the river for 10 months time and analysed for the distribution of Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn elements. The determination of extractable heavy metals in sediments was carried out by using Flame Atomic Absorption Spectrometer. The validation of the results was performed by the analysis of a BCR 701 standard reference material.     

Rare earth elements in the Rhine River, Germany: first case of anthropogenic lanthanum as a dissolved microcontaminant in the hydrosphere

The distribution of dissolved rare earth elements (REE) in the Rhine River, Germany, shows the anthropogenic gadolinium (Gd) microcontamination that is commonly observed in rivers in densely populated countries with a highly evolved health care system. However, the Rhine River also carries anomalously high concentrations of lanthanum (La), which produce very large positive La anomalies in normalized REE distribution patterns. These positive La anomalies first occur north of the City of Worms and then decrease in size downstream, but are still significant approximately 400 km downstream, close to the German-Dutch border. The strong La enrichment is of anthropogenic origin and can be traced back to effluent from a production plant for fluid catalytic cracking catalysts at Rhine river-km 447.4. This effluent is characterized by extremely high dissolved total REE and La concentrations of up to 52 mg/kg and 49 mg/kg, respectively. Such La concentrations are well-above those at which ecotoxicological effects have been observed. The Rhine River is the first case observed to date, where a river's dissolved REE inventory is affected and even dominated by anthropogenic La. Our results suggest that almost 1.5t of anthropogenic dissolved La is exported via the Rhine River into the North Sea per year. This reveals that the growing industrial use of REE (and other formerly "exotic" elements) results in their increasing release into the environment, and highlights the urgent need to determine their geogenic background concentrations in terrestrial surface waters.     

A study on the Cr(VI) removal from aqueous solutions by steel wool

The reduction of Cr(VI) by steel wool and the precipitation of reduced chromium by CaCO(3) powder and NaOH solution were investigated in continuous and batch systems, respectively. The effects of acid and initial Cr(VI) concentrations, volumetric rate and temperature of solution on Cr(VI) reduction were studied. The results showed that the reduction of Cr(VI), to a large extent, depended on, and increased with, acid concentration. The Cr(III) and iron ions in the reduced solution were completely precipitated by using NaOH solution at appropriate alkaline conditions. It was concluded that CaCO(3) powder could be used as a cheap precipitant for Cr(III) ions. But the iron ions in the reduced solution could not be fully removed by using this precipitant.     

Ecological risk assessment of heavy metals in surface sediments of northern littoral zone of Lake Çıldır,Ardahan, Turkey

In this paper, the heavy metal levels (Cu, Pb, Zn, Ni, Mn, Fe, As, Cd, Cr, Hg), organic carbon, and chlorophyll degradation products were studied to prove their ecological effects in Lake Ç?ld?r, where fossil fuels are used as an energy source in the studied area for most of the year, and domestic waste from settlements is discharged directly into the lake. Sediment samples were collected from six sites on the northern shore of Ç?ld?r Lake, Turkey in November 2012. Enrichment (EF) and contamination factor (CF) values were determined, and Pollution Load (PLI) and Potential Ecological Risk (PER) indices were calculated. Average concentrations of heavy metals in the sediments were, in descending order, Fe?>?Mn?>?Zn?>?Ni?>?Cr?>?Cu?>?Pb?>?As?>?Cd?>?Hg, respectively. According to mean values, the source of these elements may be considered natural due to lack of enrichment in Cu, Pb, Zn, Ni, and Cr in the sediment samples. Regarding enrichment of As, Cd, Mn, and Hg, the highest EF belongs to Hg. PLI and PER values indicate there are moderate ecological risk in the lake.