Utilization of the copper recovered from waste printed circuit boards as a metal precursor for the synthesis of TiO2/magnetic-MOF(Cu) nanocomposite: Application in photocatalytic degradation of pesticides in aquatic solutions.

In this study, a number of leaching solutions (H2SO4, CuSO4 and NaCl) and an electrochemical method were used together for the separation of Cu from waste printed circuit boards. Secondly, the magnetic-MOF(Cu) was synthesized using the Cu recovered from waste printed circuit boards. Thereafter, TiO2/mag-MOF(Cu) composite was prepared and its photocatalytic activity was assessed in the photo degradation of two prominent organophosphorus pesticides, namely malathion (MTN) and diazinon (DZN). The catalytic structure of the MOF-based composite was fully characterized by various analyses such as XRD, SEM, EDAX, FT-IR, VSM and UV-vis. The obtained analyses confirmed the successful synthesis of TiO2/mag-MOF(Cu) composite. The synthesized composite exhibited highly efficient in the degradation of both pollutants under the following conditions: pH 7, contaminant concentration 1 mg/L, the catalyst dosage of 0.4 g/L, visible light intensity 75 mW/cm2 and reaction time of 45 min. First order kinetic model was best suited with the experimental results (R2: 0.97-0.99 for different MTN and DZN concentrations). Trapping studies revealed that superoxide radicals (O2•-) played an important role during the degradation process. Furthermore, the catalyst demonstrated a superb recovery as well as high stability over five cyclic runs of reuse. In addition, the total organic carbon (TOC) analysis showed over 83% and 85% mineralization for MTN and DZN, respectively. The combined system of TiO2/mag-MOF(Cu)/Vis also exhibited a great level of efficiency and feasibility in the treatment of tap water and treated wastewater samples. It is concluded that TiO2/mag-MOF(Cu) could be used as an excellent catalyst for the photodegradation of MTN and DZN in aqueous solution.

A global systematic review, meta-analysis and health risk assessment on the quantity of Malathion, Diazinon and Chlorpyrifos in Vegetables.

It is widely believed that an increasing trend in the production and consumption of vegetables has led to a dramatic rise in the use of pesticides potentially threatening the health of consumers around the world. This systematic study along with meta-analysis has mainly centered on the evaluation of the quantity of three well-known pesticides namely, Malathion (MLT), Diazinon (DZN) and Chlorpyrifos (CPF) in vegetables. In this regard, a comprehensive literature search has been performed over the last decade (January 1, 2011 to June 21, 2020) within the scientific databases including PubMed, Web of Science, and Scopus. Of 1239 articles identified through the database screening, 22 plus 37 data report were retained and included in the meta-analysis phase. Additionally, the probabilistic human health risks for the consumers due to the intake of CPF, DZN and MLT from eating vegetables were estimated by the Monte Carlo Simulated (MCS) method. According to the findings, the maximum quantities of MLT, DZN and CPF in the vegetables were observed in Pakistan (222 µg/kg, 95%CI = 214.94-229.08), Thailand (245.00, 95% CI = 235.2-254.8) and South Korea (440 µg/kg, 95% CI = 437.19-442.81), while the lowest concentration levels were reported in China (1.7 µg/kg, 95% CI = 1.56-1.84), Poland (0.57, 95% CI = 0.46-0.68) and Poland (5.78 µg/kg, 95% CI = 4.40-7.12), respectively. The results of the Egger's and the Begg's tests revealed that no bias with regard to the potential publication was observed. Finally, non-carcinogenic risk assessment results demonstrated that the exposure to the studied pesticides thorough vegetables consumption could not threaten the health of consumers.

Littered cigarette butt as a well-known hazardous waste: A comprehensive systematic review.

Most of cigarettes used in the world have filters. Following smoking, the cigarette butts (CBs) are often littered as wastes in the environment. CBs generally contain several toxic substances that are trapped in the cigarette filter. Filters are made of non-biodegradable materials and remain in the environment for a long time. Within this study, it is attempted to systematically review the articles on CBs and find out the answers to the problems associated with the factors including quantity, distribution, origin and toxicity of CBs in the environment. It is estimated that approximately 5.5 trillion cigarettes are being produced annually in the world and the CB wastes would reach 1.2 million tons and increase by 50% until 2025. CBs contain thousands of dangerous chemicals such as arsenic, benzene, hydrogen cyanide, PAHs, pyridine, heavy metals and so forth. It is also believed that eachCB can pollute 1000 liters of water. Given the inadequacy of mechanical equipment as well as the cost of collecting these wastes, there should be a special focus on these items as follows: producing cigarettes with degradable filters, reducing the rate of smoking in the world, reducing the toxic and chemical substances in the process of plant growth, processing and production of cigarettes, training people to discard CBs properly, putting legal and financial pressures on cigarettes production, and the last but not least, providing effective solutions for collecting CBs.

Simultaneous derivatization and extraction of nitrophenols in soil and rain samples using modified hollow-fiber liquid-phase microextraction followed by gas chromatography-mass spectrometry.

A simple and sensitive method based on a modified hollow-fiber liquid-phase microextraction followed by gas chromatography-mass spectrometry has been successfully developed for the extraction and simultaneous derivatization of some nitrophenols (NPs) in soil and rain samples. Microwave-assisted solvent extraction was used for the extraction of NPs from the soil, while the rain sample was directly applied to the previously mentioned method. Briefly, in this method, the analytes were extracted from aqueous samples into a thin layer of organic solvent (dodecane + 10% tri-n-octylphosphine oxide) sustained in the pores of a porous hollow fiber. Then, they were back-extracted using a small volume of organic acceptor solution (25 µl; 10 mg/L N-methyl-N-(trimethylsilyl)trifluoroacetamide, as derivatization reagent, in acetonitrile) that was located inside the lumen of the hollow fiber. Under the optimized extraction conditions, enrichment factors of 255 to 280 and limits of detection of 0.1 to 0.2 µg/L (S/N = 3) with dynamic linear ranges of 1-100 µg/L were obtained for the analytes. The accuracy of the approach was tested by the relative recovery experiments on spiked samples, with results ranging from 93 to 113%. The method was shown to be rapid, cost-effective, and potentially interesting for screening purposes.

Generic approach for the sensitive absolute quantification of large undigested peptides in plasma using a particular liquid chromatography-mass spectrometry setup.

A generic LC-MS approach for the absolute quantification of undigested peptides in plasma at mid-picomolar levels is described. Nine human peptides namely, brain natriuretic peptide (BNP), substance P (SubP), parathyroid hormone 1-34 (PTH), C-peptide, orexines A and B (Orex-A and -B), oxytocin (Oxy), gonadoliberin-1 (gonadothropin releasing-hormone or luteinizing hormone-releasing hormone, LHRH) and α-melanotropin (α-MSH) were targeted. Plasma samples were extracted via a 2-step procedure: protein precipitation using 1vol of acetonitrile followed by ultrafiltration of supernatants on membranes with a MW cut-off of 30 kDa. By applying a specific LC-MS setup, large volumes of filtrates (e.g., 2×750 µL) were injected and the peptides were trapped on a 1mm i.d.×10 mm length C8 column using a 10× on-line dilution. Then, the peptides were back-flushed and a second on-line dilution (2×) was applied during the transfer step. The refocalized peptides were resolved on a 0.3mm i.d. C18 analytical column. Extraction recovery, matrix effect and limits of detection were evaluated. Our comprehensive protocol demonstrates a simple and efficient sample preparation procedure followed by the analysis of peptides with limits of detection in the mid-picomolar range. This generic approach can be applied for the determination of most therapeutic peptides and possibly for endogenous peptides with latest state-of-the-art instruments.

Quantitation of valproic acid in pharmaceutical preparations using dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detection without prior derivatization.

Dispersive liquid-liquid microextraction (DLLME), coupled with gas chromatography-flame ionization detection (GC-FID), has been successfully used for the extraction and determination of valproic acid (VPA) in pharmaceutical preparations. In the developed method, an appropriate mixture of extracting and disperser solvents was rapidly injected into an aqueous sample. Having formed a cloudy solution, the mixture was centrifuged and then the extracting solvent was sedimented at the bottom of a conical test tube. The extract was then injected into a GC system directly, without any further pretreatment. Initially, microextraction efficiency factors were optimized and the optimum experimental conditions found were as follows: tetrachloroethylene (9.0 µL) as extracting solvent; acetone (1.0 mL) as disperser solvent; 5 mL acidic aqueous sample (pH 1) without salt addition. Under the selected conditions, the calibration curve showed linearity in the range of 0.1-5.0 mg/L with regression coefficient corresponding to 0.9998. The limit of detection was found to be 0.05 mg/L. Finally, the method was applied for the determination of VPA in two different pharmaceutical preparations. A reasonable intra-assay (3.9-10.8%, n = 3) and inter-assay (5.6-11.4%, n = 3) precision illustrated the good performance of the analytical procedure. The protocol proved to be rapid and cost-effective for screening purposes.

Quantitation of mononitrotoluenes in aquatic environment using dispersive liquid-liquid microextraction followed by gas chromatography-flame ionization detection.

A simple and efficient method (known as dispersive liquid-liquid microextraction (DLLME)) combined with gas chromatography-flame ionization detector (GC-FID) has been successfully developed for the extraction and determination of mononitrotoluenes (MNTs) in aquatic samples. The effects of parameters such as the nature and volume of the extracting and disperser solvents on the microextraction efficiency were also investigated. The volume of the extracting solvent (chlorobenzene) and that of the disperser solvent (acetonitrile) were obtained to be equal to 10.0 microL and 0.5 mL, respectively, in the optimal microextraction conditions established. Under the optimal conditions, the detection limit of the method was 0.5 microg L(-1) and the relative standard deviations (RSDs%) for determination of the MNTs were in the range of 8.0-9.4. Linearity was found to be in the range of 1-1000 microg L(-1); also, the pre-concentration factors were in the range of 351-357. Finally, the method was applied to determine the trace amounts of the MNTs in several real aquatic samples and satisfactory results were obtained.