Comparison of phenanthrene biodegradation by free and immobilized cell systems: formation of hydroxylated compounds

One of the foremost environmental issues having a key role in the feasibility study of polycyclic aromatic hydrocarbons (PAHs) biodegradation is the concern of the toxicity of the formed intermediate metabolites. In this study, biodegradability of phenanthrene (PHE) at initial concentrations of 100–500 ppm and its hydroxylated intermediate metabolites (IMs) in aqueous phase were investigated using free cells (FC) and immobilized cells (IC) in polyvinyl alcohol (PVA) cryogel beads. Results showed that both FC and IC systems were capable of complete PHE biodegradation at initial concentrations lower than 250 ppm after 7 days, though IC system showed a higher PHE removal rate. The maximum IM concentrations observed at initial PHE concentrations of 100 and 250 ppm were 20 and 49 ppm for FC system, whereas 7.4 and 19 ppm were obtained for IC system, respectively, and IMs were finally removed after 7 days. Similarly, at 500 ppm, IC system resulted in higher removal of PHE compared to FC system. However, during the 7-day period for FC system, IMs concentration rose up to 59 ppm, while for IC system, IMs concentration reaches a maximum at day 5 and thereafter it follows a negative rate. It was also shown that resorcinol as an indicator of hydroxylated aromatic metabolites at concentrations of 0–100 ppm can well be biodegraded by free and immobilized cell systems. No prohibition on PHE biodegradation could hence occur due to IMs formation. Additionally, stability of IC system was examined in repeated-batch cultures, showing the effective removal of PHE up to nine reuse cycles.     

Susceptibility mapping of groundwater salinity using machine learning models

Environmental Science and Pollution Research - Increasing groundwater salinity has recently raised severe environmental and health concerns around the world. Advancement of the novel methods for...     

Preparation of the Mn/Co mixed oxide catalysts for low-temperature CO oxidation reaction

The Mn/Co mixed powders with various Mn/Co molar ratios were prepared by the coprecipitation method and used in low-temperature CO oxidation. The physicochemical characteristics of these powders were characterized using the Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), temperature-programmed reduction (TPR), and scanning electron microscopy (SEM) analyses. The results demonstrated that the Mn/Co molar ratio significantly affected both the textural and catalytic properties and the sample with a Mn/Co = 1:1 possessed a BET area of 123.7 m²g⁻¹ with a small mean pore size of 6.44 nm. The catalytic results revealed that the pure cobalt and manganese catalysts possessed the low catalytic activity and the pure Co catalyst is not active at temperatures lower than 140 °C. The highest catalytic activity was observed for the catalyst with a Mn/Co = 1. The obtained results showed that the incorporation of Pd into the Mn/Co catalyst significantly enhanced the catalytic activity for oxidation of carbon monoxide and the highest CO conversion was observed for the catalyst with 1 wt.% Pd and this catalyst exhibited a CO conversion of 100% at 80 ^°C.

     

Investigating utility level of waste disposal methods using multicriteria decision-making techniques (case study: Mazandaran-Iran)

Journal of Material Cycles and Waste Management - Regardless of collection and disposal systems of wastes, which are the main causes of pollution in cities and villages, attention to the health and...     

Content of potentially toxic elements (PTEs) in various animal meats: a meta-analysis study,systematic review,and health risk assessment

Environmental Science and Pollution Research - Meat comprises the main part of the diet in many countries around the world. The present study aimed to assess potentially toxic elements (PTEs) lead...     

Effects of alkali promoters on the textural and catalytic properties of mesoporous Fe–Al–Cu catalysts for water gas shift reaction

Mesoporous Fe₂O₃–Al₂O₃–CuO catalysts promoted with alkali oxides were synthesized and used in water gas shift reaction (WGSR) at high temperatures for hydrogen purification. These chromium-free catalysts were characterized using nitrogen adsorption/desorption, hydrogen temperature programmed reduction, X-ray diffraction (XRD), and transmission electron microscopy techniques. The synthesized catalysts with narrow single-modal pore size distribution in mesopore region possessed high specific surface area. The catalytic results revealed that except Cs, the addition of other alkali promoters declined the catalytic activity. However, all catalysts showed higher catalytic performance than the conventional commercial catalyst. The results showed an optimum content of Cs promoter (3 wt.%) for the promoted Fe–Al–Cu catalyst (3 wt.% Cs-FAC), which exhibited the highest activity in WGSR at high temperature.     

Protective effect of Zingerone against mouse testicular damage induced by zinc oxide nanoparticles

Environmental Science and Pollution Research - The purpose of the present study was to evaluate the effect of Zingerone (Zing) on zinc oxide nanoparticle (ZNP)-induced spermatogenesis defects in...     

What is a static head measurement? Evaluating structural error and implications for regional groundwater modeling

Most groundwater modelers avoid using static heads measured from active production wells because they can introduce a bias into model calibration. However, in the deep confined Cambrian-Ordovician Sandstone Aquifer System in the Central Midcontinent of North America, dedicated observation wells are sparse and remote from areas of most concentrated pumping. As a result, in areas where drawdown is the greatest and modeling is most needed, only static heads from production wells are available for calibration. This paper evaluates two leading sources of discrepancies in using production well data, spatial and temporal structural error (S.E.). A simple Theis solution is used to evaluate the potential magnitude of spatial S.E. when calibrating a regional MODFLOW model with coarse cell resolution. Despite theoretical analyses indicating that spatial S.E. could be significant, statistical analysis of the model results suggests that temporal S.E. is dominant. Long (ranging over decades) or frequent (monthly) head datasets are key in understanding temporal S.E., to better capture water-level variability. In this study, the range in static head observations impacted estimates of the remaining time a well could extract water from the aquifer by 0.1 to 16.0 years. This uncertainty in future water supply is highly relevant to stakeholders and must be assessed in hydrographs depicting risk.     

Determination of <Superscript>90</Superscript>Sr in milk and milk powder in Tehran and estimation of annual effective dose

Thirty-eight different milk and milk powder samples from Tehran-Iran were collected and analyzed for ⁹⁰Sr activity using a method in which the daughter product of ⁹⁰Sr decay (⁹⁰Y) was extracted by tributyl phosphate from ashed milk. ⁹⁰Y was then back extracted with water, and oxalate was precipitated . Following the sample analyzing, beta counting was performed with an ultralow-level liquid scintillation spectrometer. The quality control and assurance of the method were obtained by standard samples prepared with an IAEA-certified reference material. The mean determined ⁹⁰Sr activity concentration in the analyzed milk and milk powder (0.225 ± 0.042 and 0.216 ± 0.024 Bq kg⁻¹, respectively) showed that the radioactivity concentration in our samples was too low to induce biological hazards. These data can provide useful information of the background level of contamination, which in turn can be used in the following environmental monitoring programs.     

One-pot hard template synthesis of mesoporous spinel nanoparticles as efficient catalysts for low temperature CO oxidation

Co-Fe, Cu-Cr, and Co-Mn mixed oxide catalysts were prepared using a one-pot hard template synthesis method, and their catalytic performance was investigated before and after the rearrangement of the template. To evaluate the structural properties of the catalysts, various analyses were employed, including the BET, XRD, H₂-TPR, FE-SEM, EDX, and X-ray digital mapping of the elements. The results indicated that the rearrangement of the catalyst structure had a profound effect on the structural and catalytic properties, so that in all three synthesized catalysts, the specific surface and the reducibility increased significantly, and the crystalline structure and morphology of the catalysts changed remarkably. The specific surface area of the CoFe, CuCr, and CoMn catalysts increased from 3.5, 1.1, and 72.9 m²/g to 151.3, 52.8, and 108.0 m²/g, respectively. These structural changes significantly increased the catalytic performance. The results indicated that the 100% conversion temperature of the CoMn catalyst as the optimal sample after rearrangement was reduced from 250 to 125 °C. Also, the stability of the CoMn catalyst in dry and wet conditions was investigated and the results indicated that the presence of water vapor reduced the activity and stability of the catalyst. The activation energy was also calculated on Co-Mn catalyst (59.5 kJ/mol) and the results confirmed that the most probable mechanism for this reaction was the MVK mechanism.