The relationship between chronic exposure to arsenic through drinking water and hearing function in exposed population aged 10-49 years: A cross-sectional study.

It has been documented that arsenic has a potential risk to human health and identified as a risk factor for hearing impairment. However, there are few studies that confirm the ototoxic effect of arsenic, especially on the human auditory system. Therefore, the current study was conducted to investigate the correlation between auditory thresholds at different frequencies (0.25, 0.5, 1, 2, 4 and 8 kHz) and arsenic levels in drinking water samples. A total of 240 people, divided into two equal groups: exposed and reference, were selected for the auditory tests. It should be noted that, at frequencies from 0.25 to 1 kHz, no hearing loss was observed in the both groups. Based on the results, no significant correlations (p > 0.05) were found between hearing thresholds and confounding variables including gender and BMI. However, smoking and age are known to be the main variables for hearing loss in univariate regression analysis. In the case of age, the hearing loss risk in the older participants was increased compared with the younger participants (4 kHz (OR =1.09; 95% CI: 1.04, 1.13) and 8 kHz (OR =1.12; 95% CI: 1.06, 1.18)). Smoking habits had significant associations with hearing loss risk at 4 kHz (OR = 3.48; 95% CI: 1.47, 8.22) and 8 kHz (OR = 3.01; 95% CI: 1.14, 7.95). The multivariate regression analysis showed that age, smoking status, and exposure to arsenic were significantly associated with increased risk of hearing loss. Moreover, no statistically significant correlation (p˃0.05) was observed between arsenic exposure and hearing loss in the logistic regression model compared to the reference group. These outcomes suggest that further investigation and cohort studies with a larger number of participants should be conducted to find an association between arsenic exposure and hearing loss in general population.

The catalytic ozonation of diazinon using nano-MgO@CNT@Gr as a new heterogenous catalyst: the optimization of effective factors by response surface methodology.

In this research, the degradation of the insecticide diazinon was studied using a new hybrid catalyst consisting of magnesium oxide nanoparticles (nano-MgO), carbon nanotubes (CNTs), and graphite (Gr), nano-MgO@CNT@Gr, under various experimental conditions. This study shows the optimization of the nano-MgO@CNT@Gr/O3 process for diazinon degradation in aqueous solutions. Box-Behnken experimental design (BBD) and response surface methodology (RSM) were used to assess and optimize the solo effects and interactions of four variables, pH, catalyst loading, reaction time, and initial diazinon concentration, during the nano-MgO@CNT@Gr/O3 process. Analysis of regression revealed an adequate fit of the experimental results with a quadratic model, with R 2 > 0.91. Following the collection of analysis of variance (ANOVA) results, pH, catalyst loading, and reaction time were seen to have significant positive effects, whereas the concentration of diazinon had a considerable negative impact on diazinon removal via catalytic ozonation. The four variables for maximum diazinon removal were found to be optimum (82.43%) at the following levels: reaction time, 15 min; pH, 10; catalyst dosage, 1.5 g L-1; and diazinon concentration, 10 mg L-1. The degradation of diazinon gave six kinds of by-products. The mechanism of diazinon decomposition was considered on the basis of the identified by-products. According to these results, the nano-MgO@CNT@Gr/O3 process could be an applicable technique for the treatment of diazinon-containing wastewater.

A comparative study for the removal of imidacloprid insecticide from water by chemical-less UVC, UVC/TiO2 and UVC/ZnO processes.

BACKGROUND: Chloronicotinic insecticide are a class of pesticides that are commonly used as insecticides. Among the frequently used chloronicotinic pesticide, imidacloprid (IM) was developed in 1986. The residual of this insecticide or any pesticides may have serious public health threats. METHODS: Both degradation and mineralization of the imidacloprid (IM) in aqueous solution was studied under various experimental conditions using different advanced oxidation processes namely, ultraviolet C (UVC), UVC + TiO2, and UVC + ZnO. All the experiments were performed using a lab-scale batch photoreactor with a working volume of 100 mL equipped with low-pressure mercury vapor lamp (9 W, 18 cm long, Philips Co.), emitting UV radiation with maximum intensity at 254 nm. The possible intermediates and a reaction pathway for photocatalytic degradation of the IM were also evaluated. RESULTS: It was observed that under optimal condition for UVC/TiO2 process (C0 = 100 mg/L, pH = 7.5, t = 20 min, TiO2 dose = 100 mg/L), IM was effectively degraded (88.15%) and followed the first order kinetics model. The degradation efficiency increased with increasing of illumination time and is more favorable in alkaline pH compared to acidic pH. Degradation of the IM in photocatalytic process was compared with photolysis showing a significant synergy effect in the case of the photocatalytic degradation process, leading at 20 min illumination time to a 36.7% increase of the IM removal efficiency in comparison to the single UVC. The GC/MS chromatograms before and after treatment confirmed the effectiveness of the UVC/TiO2 process in simplifying the nature of IM and its conversion to more simple and degradable compounds. CONCLUSION: The heterogeneous UVC/TiO2 process was found to be an efficient chemical-less method that is appropriate for degradation of IM from aqueous phase.

Pentachlorophenol removal from aqueous solutions by microwave/persulfate and microwave/H2O2: a comparative kinetic study.

Pentachlorophenol (PCP) is one of the most fungicides and pesticides used in wood protection. Poisoning from PCP may be happened in dermal absorption, and respiration or ingestion. With regard to health and environmental effects of PCP, many methods were studied for its removal. Microwave assisted other methods are environmental friendly, safety, and economical method, therefore, in this study; a modified domestic microwave assisted hydrogen peroxide (MW/H2O2) and sodium persulfate (MW/SPS) was used for PCP removal from aqueous solutions. PCP removal rate was measured under different factors such as pH, energy intensity, SPS, H2O2 concentration, Tert- butyl alcohol (TBA) and chemical oxygen demand (COD). The concentration changes of PCP were determined using spectrophotometer and HPLC spectra, respectively. The best removal PCP rate obtained in condition of pH of 11, 0.02 mol L(-1) of SPS, 0.2 mol L(-1) of H2O2 and energy intensity of 600 W. Moreover, COD removals in MW/H2O2 and MW/SPS process were 83% and 94%, respectively, also TBA test decreased 15% and 3% of PCP removal in MW/SPS and MW/H2O2 processes respectively. Experimental results indicated that sulfate radical was stronger than hydroxyl radical and examinations order reaction was in first order. In this study, was cleared that MW/SPS process was more effective than MW/H2O2 process in PCP removal.

Microwave/H2O2 efficiency in pentachlorophenol removal from aqueous solutions.

BACKGROUND: Pentachlorophenol (PCP) is one of the most fungicides and pesticides. Acute and chronic poisoning from PCP may be occurred by dermal absorption, and respiration or ingestion. With respect to health and environmental effects of PCP, many methods were considered regarding its removal. Microwave assisted other methods are environmental friendly, safety, and economical method, consequently, in this study; microwave assisted with hydrogen peroxide (MW/H2O2) was used for PCP removal from aquatic solutions. METHODS: The possible of PCP removal was considered by application of a modified domestic microwave. PCP removal rate was considered under different factors such as H2O2 dose (0.01, 0.02, 0.1, 0.2, 0.3 mol/L), PCP concentration (100,200, 300, 400, 500, 750, 1000 mg/L), pH (3, 7, 11), energy intensity (180,450, 600 W), COD (344 mg/L), and scavenger testes (0.02 mol/L from each of Tert- butyl alcohol (TBA), NaCl, NaHCO3, and Na2CO3). The concentration changes of PCP were determined using spectrophotometer and HPLC spectra, respectively. RESULTS: The best PCP removal was obtained in condition of pH 11, 0.2 mol/L H2O2, and 600 W energy intensity. Moreover, COD removal in this condition was 83%. Results obtained from radical scavengers indicated that OH° had only an initiator role, and had not a dominant role, and order reaction was in first order. CONCLUSIONS: The results of microwave/H2O2 application showed that this process is suitable for removal of PCP and other chlorinated organic compounds in alkaline pH.