An electrochemical sensor for the determination of environmentally hazardous fungicide pyrimethanil in water and fruit samples.

We developed a facile electroanalytical system for the rapid and sensitive detection of pyrimethanil through the modification of carbon paste electrode surface using the as-fabricated europium doped feather-type CuO nanoflowers (FT-Eu3+-CuO NF sensor). The peak current of pyrimethanil oxidation was elevated by the sensor due to the integration of appreciable electrochemical features of the modifier, which indicates the high ability of the modified electrode to enhance the sensitivity of pyrimethanil detection. The pyrimethanil sensor under the optimized setting had a broad linear dynamic range (0.001-800.0 µM) and a narrow limit of detection (0.18 nM). The practical applicability of the as-fabricated electrode was verified by sensing pyrimethanil in real samples; it also exhibited commendable specificity, stability and reproducibility.

Photocatalytic degradation of ciprofloxacin by MMT/CuFe2O4 nanocomposite: characteristics, response surface methodology, and toxicity analyses.

The photocatalytic degradation of ciprofloxacin (CIP) was examined by loading spinel ferrite copper (CuFe2O4) nanoparticles onto montmorillonite (MMT) under irradiation using UV light. The laboratory parameters were optimized using response surface methodology (RSM), and maximum efficiency (83.75%) was achieved at a pH of 3, CIP concentration of 32.5 mg/L, MMT/CuFe2O4 dose of 0.78 g/L, and irradiation time of 47.50 min. During the photocatalysis process, the experiments on radical trapping demonstrated the generation of hydroxyls (•OH), superoxide (•O2-) radical, electrons (e-), and holes (h+). A low rate drop (below 10%) in the CIP degradation during the six consecutive reaction cycles corroborated the remarkable recyclability and stability of the MMT/CuFe2O4. The acute toxicity of the treated solution was determined using Daphnia Magna, by applying photocatalysis, which was indicative of a marked decline in the toxicity. Comparing the findings of the degradation using UV and the degradation process using visible light represented results with close resemblance to each other at the end of the reaction time. Besides, under UV and visible light, the particles in reactor are easily activated when the pollutant mineralization exceeded 80%.

The application of a new recyclable photocatalyst γ-Fe2O3@SiO2@ZIF8-Ag in the photocatalytic degradation of amoxicillin in aqueous solutions.

This pilot study synthesized the γ-Fe2O3@SiO2@ZIF8-Ag nanocomposites via the hydrothermal method to study its potential use in amoxicillin degradation as a novel photocatalyst in aqueous solutions under visible light radiation. Various diagnostic methods were used to determine the morphology and functional structure of the photocatalyst, and the results confirmed its proper formation. Complete degradation of AMX was obtained at a pH of 5, catalyst dosage of 0.4 g/L, AMX concentration of 10 mg/L, and reaction time of 60 min. The efficiency of the degradation was diminished when anions were present in the reaction medium, and the order of their effect was SO42- < Cl- < NO3- < HCO3-. Biodegradability (BOD5/COD ratio) increased from 0.20 to 0.68 after 120 min of photocatalytic treatment, with a COD removal of 87.54% and a TOC removal of 74.88%. Through the experimental trapping of electrons, we found the production of reactive species, such as hydroxyl radical (•OH), superoxide (O2•-), and holes (h+), in the photocatalysis reactor and that •OH was the predominant species in AMX photodegradation. Comparative experiments emphasized that the oxidation process occurs with the adsorption of pollutants on the surface of the catalyst, and the photocatalyst has the potential to be activated by various light sources, including visible light, UV light, and sunlight, with an AMX decomposition above 88%. The synthesized particles can be recovered after five consecutive cycles with minimal reduction in the degradation rate (< 4%). γ-Fe2O3@SiO2@ZIF8-Ag can be considered a promising photocatalyst for use in AMX degradation due to its recyclability, easier activation by different light sources, and excellent mineralization.

Removal of Benzene and Toluene from Synthetic Wastewater by Adsorption onto Magnetic Zeolitic Imidazole Framework Nanocomposites.

Considering the risk associated with exposure to benzene and toluene in water resources, researchers have been motivated to conduct studies to remove them from aqueous solutions. Thus, by performing the present study, the potential of Fe3O4/zeolite imidazolate framework nanoparticles (Fe3O4@ZIF-8) was evaluated for the adsorption of benzene and toluene. Accordingly, the solution pH, Fe3O4@ZIF-8 dosage, mixing time, concentration of benzene and toluene, and temperature, were the parameters considered for conducting the batch experiments, for which their effect on adsorption efficiency was evaluated. Our conducted experiments introduced the neutral pH as the best pH range to obtain the maximum removal. Fitting the adsorption data into the various models revealed the aptness of the Langmuir isotherm equation in describing experimental information and highest adsorption capacity; for benzene it was 129.4, 134.2, 137.3, and 148.2 mg g-1, but for toluene it was 118.4, 125.2, 129.6, and 133.1 mg g-1, for temperature 20, 30, 40, and 50 °C, respectively. Using obtained optimal conditions, the adsorption efficiencies of benzene and toluene were obtained to be 98.4% and 93.1%, respectively. Kinetic studies showed acceptable coefficients for PSO kinetics and confirmed its suitability. Also, the recyclability results showed that for six consecutive periods of the adsorption-desorption process, the percentage of removal decreased by only 6% for benzene and toluene. Moreover, calculating thermodynamic parameter changes for benzene and toluene removal confirmed the favorability and spontaneity of the studied process and its endothermic nature. Considering the above findings, Fe3O4@ZIF-8 was found to be an operative adsorbent for removing pollutants.

Efficient photocatalytic degradation of metronidazole in wastewater under simulated sunlight using surfactant- and CuS-activated zeolite nanoparticles.

Hexadecyltrimethylammonium-bromide-activated zeolite nanoparticles coated with copper sulfide (ZEO/HDTMA-Br/CuS) was evaluated as a photocatalyst under sunlight for the degradation of metronidazole (MET). The surface and structural characteristics of ZEO/HDTMA-Br/CuS and other materials used in this study were analyzed using field emission-scanning electron microscopy, Fourier transform infrared and ultraviolet-visible diffuse reflectance spectroscopies, X-ray diffraction, Brunauer-Emmett-Teller surface area and Barrett-Joyner-Halenda pore size and volume analyses, and pH of zero charge test. ZEO/HDTMA-Br/CuS exhibited excellent surface and structural catalytic properties. For a comprehensive study of the degradation process, several parameters, such as the pH (3-11), MET concentration (10-30 mg/L), ZEO/HDTMA-Br/CuS dose (0.005-0.1 g/L), reaction time (5-200 min), and H2O2 concentration (50-200 mg/L), were optimized. ZEO/HDTMA-Br/CuS achieved 100% degradation efficiency when 10 mg/L MET was used under the optimum conditions: pH = 7, ZEO/HDTMA-Br/CuS dose = 0.01 g/L, and reaction time = 180 min. The degradation efficiency increased when the concentration of H2O2 was increased from 50 to 150 mg/L and decreased with further increase to 200 mg/L, indicating that the efficiency of MET degradation highly depends on the concentration of H2O2 in an aqueous solution. The degradation kinetics analysis revealed that the degradation is of the pseudo first-order. Thus, ZEO/HDTMA-Br/CuS proved to be an exceptional catalyst for the photodegradation of MET in aqueous media.

Capability of copper-nickel ferrite nanoparticles loaded onto multi-walled carbon nanotubes to degrade acid blue 113 dye in the sonophotocatalytic treatment process.

In this study, copper-nickel ferrite (CuNiFe2O4) nanoparticles were successfully loaded onto multi-walled carbon nanotubes (MWCNTs) by using the coprecipitation method and used as new catalysts (MWCNT-CuNiFe2O4) in the sonophotocatalytic degradation process of the acid blue 113 (AB113) dye. The success of the MWCNT-CuNiFe2O4 synthesis and its properties were determined by analyzing it using field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR). A high efficiency of dye removal (100%), total organic carbon (93%), and chemical oxygen demand (95%) were achieved with the following conditions: pH of dye solution = 5, MWCNT-CuNiFe2O4 dosage = 0.6 g/L, AB113 dye concentration = 50 mg/L, UV light intensity = 36 W, ultrasonic wave frequency = 35 kHz, and treatment time = 30 min. The kinetic results revealed that the efficiency of the sonophotocatalytic process using MWCNT-CuNiFe2O4 was higher than that of the sonolysis, photolysis, photocatalysis, and sonocatalysis processes. Scavenging studies demonstrated that the holes (h+) and hydroxyl radical (•OH) were the main reactive species for the AB113 dye degradation. The stability and recyclability of MWCNT-CuNiFe2O4 were confirmed with eight consecutive cycles for a maximum efficiency of more than 92%. The high rate of BOD5/COD indicated that the sonophotocatalytic process had the potential to degrade the dye into degradable compounds. The toxicity study with an Escherichia coli growth inhibition rate emphasized that MWCNT-CuNiFe2O4 in the sonophotocatalytic degradation process of the AB113 dye had a significant effect on reducing toxicity, when compared to processes of photolysis and photocatalysis. During the sonophotocatalytic process using MWCNT-CuNiFe2O4, the AB113 dye was mineralized into CO2, H2O, NH4+, NO3-, and SO42-. The results of the present study proved that the MWCNT-CuNiFe2O4-based sonophotocatalytic process was a promising dye degradation technology to protect the aquatic environment.

Activated carbon derived from Azolla filiculoides fern: a high-adsorption-capacity adsorbent for residual ampicillin in pharmaceutical wastewater.

In this study, the effectiveness of activated carbon prepared from the Azolla filiculoides fern (ACAF) in order to remove ampicillin from aqueous solution was examined. The preparation of the ACAF was performed through chemical and physical activation processes with the presence of ZnCl2 and at a temperature of 450 °C. The ACAF yield was 44.7% of the fresh Azolla filiculoides. The results obtained from the characterization study indicate that the prepared ACAF has excellent surface and internal properties to be used as an adsorbent. The surface area, porosity, and pore volume were estimated to be 716.4 m2/g, 51.2%, and 0.621 cm3/g, respectively. The functional groups in ACAF that were responsible for the adsorption of ampicillin molecules were detected using FTIR analyses. The maximum efficiency (96.84%) and uptake (114.3 mg/g) of ACAF to remove ampicillin were achieved under the following conditions: ACAF dose = 0.8 g/L, pH = 7, concentration of ampicillin = 100 mg/L, contact time = 60 min, and temperature = 45 °C. It was found that the kinetic and isotherm data matched the pseudo-second-order and Langmuir models with high precision values, respectively. Considering the thermodynamics of the adsorption, the endothermic and spontaneous nature of the ampicillin adsorption onto ACAF was approved. The ampicillin adsorption capacity by ACAF was not significantly affected by the presence of different concentrations of NaNO3 competitor ion. The considerably higher adsorption capacity of the ACAF for ampicillin (114.3 mg/g) than other previously used adsorbents with excellent regeneration level (five cycles) depicts the superior performance of ACAF in the adsorption systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13399-021-01962-4.

Development of sonophotocatalytic process for degradation of acid orange 7 dye by using titanium dioxide nanoparticles/graphene oxide nanocomposite as a catalyst.

In the present study, the sonophotocatalytic degradation of acid orange 7 (AO7) dye was evaluated. The catalyst used was the titanium dioxide nanoparticles/graphene oxide (TiO2/GO) nanocomposite, which was synthesized using the Hummers and Hoffman's method and the liquid phase deposition method. TiO2/GO nanocomposite was characterized through the analyses of transmission electron microscopy (TEM), X-ray diffraction (XRD), Energy Dispersive X-ray (EDX) spectroscopy, Raman spectroscopy, and Fourier transform infrared (FTIR) spectroscopy. In addition, properties of the surface area and pore size were determined by N2 adsorption-desorption and the Barrett-Joyner-Halenda methods. After modification, the nanocomposite properties showed successful stabilization of TiO2 on the graphene substrate and reduction of the recombinant carrier loads. By utilizing the proposed treatment, complete degradation of AO7 could be achieved under optimal operating parameters (pH = 5, initial concentration of AO7 dye = 50 mg/L, TiO2/GO nanocomposite dose = 0.5 g/L, UV light intensity = 36 W, ultrasonic wave intensity = 35 kHz, and reaction time = 30 min). Scavenging experiments confirmed that OH and h+ radicals were the predominant species in the sonophotocatalytic degradation reactions of the AO7 dye. The stability study confirmed the excellent shelf life of the TiO2/GO nanocomposite, with only a slight reduction in the degradation efficiency of the AO7 dye (<8.27%) detected, after six consecutive cycles of the sonophotocatalytic process. Studies related to the degradability of the AO7 dye and the biodegradability of the effluent from the process showed that the applied sonophotocatalytic system was able to remove the TOC concentration by 83% after a reaction time of 30 min. Moreover, the increase in the BOD5/COD ratio was also a confirmation for the increase in biodegradability of the treated AO7 dye effluent. Finally, the toxicity test showed that the growth inhibition rate of Escherichia coli (E. coli), as a viability index, decreased to about 7.34% after a reaction time of 180 min. This result indicated the formation of compounds with low toxicity and molecular weight over the reaction time of the sonophotocatalytic process of AO7 dye.

The biosorption of reactive red dye onto orange peel waste: a study on the isotherm and kinetic processes and sensitivity analysis using the artificial neural network approach.

The agricultural waste of orange peels (OPs) was utilized as a cheap biosorbent and then tested for its ability to treat the reactive red (RR) dye wastewater. Several experiments were done to get the equilibrium isotherm and kinetic-relevant data. In addition, several experimental factors such as solution pH, temperature, contact time, and initial RR dye concentration were studied, in light of their impact on the biosorption process. The utilized isotherm and kinetic models were evaluated by using the chi-square test and coefficient of determination parameters for their representation of real data. In addition, the obtained data of their biosorption capacities, at different conditions, were modeled by the artificial neural network (ANN) approach. The results of the isotherm study revealed that the experimental data can be best accounted by both the Langmuir and Temkin models, demonstrating that the RR molecules were sorbed to two or more different types of biosorption sites of OP. The kinetic study for determining the characteristics of the rate of diffusion demonstrated that the intraparticle diffusion process was not the sole rate-limiting step in the biosorption of the RR dye-OP couple. Furthermore, the biosorption process was chemisorption in nature, as the pseudo-second-order reaction proved to be the best representative model for the kinetic data. The outcome of modeling also assumed that using the ANN tool was useful to reproduce the data again and foretell the manner in which biosorption behaved. According to the results of the Langmuir model, it was found that the maximum OP uptake for the biosorption of the RR dye was up to 82 mg/g, observed at optimized values of the experimental parameters. Such prior results highlight that OP is an effective agent of biosorption in the elimination of RR dyes from polluted solutions, moreover, in a cost-effective manner.

A comprehensive study on the application of FeNi3@SiO2@ZnO magnetic nanocomposites as a novel photo-catalyst for degradation of tamoxifen in the presence of simulated sunlight.

Pharmaceutical compounds at trace concentrations are found in the environment, especially in drinking water and food, posing significant negative effects on humans as well as on animals. This paper aimed to examine the diagnostic catalytic properties and efficacy of a novel synthesized photocatalyst, namely FeNi3@SiO2@ZnO magnetic nanocomposite, for the removal of tamoxifen (TMX) from wastewater under simulated sunlight. According to the results, it was found that TMX was completely degraded operating under optimized conditions (i.e. pH = 7, catalyst dose = 0.01 g/L, initial TMX concentration = 20 mg/L and reaction time = 60 min). The reaction kinetics of TMX degradation followed a pseudo-first order kinetics model. The final by-products from the TMX photodegradation were water, carbon dioxide, acetic acid, nitroacetic acid methyl ester, 2-methyl-2-pentenal, and 4-methyl-2-pentanol. In addition, the synthesized photocatalyst could successfully performed five consecutive photodegradation cycles. The obtained results revealed that the synthesized FeNi3@SiO2@ZnO magnetic nanocomposite holds a great potential to be applied as a photocatalyst for the degradation of TMX on an industrial scale.

The practical utility of the synthesis FeNi3@SiO2@TiO2 magnetic nanoparticles as an efficient photocatalyst for the humic acid degradation.

Humic acid (HA) compounds in drinking water and wastewater disinfection processes are viewed as precursors of highly toxic, carcinogenic, and mutagenic disinfection by-product chemicals. In recent times, these compounds have gained considerable attention of scientists for their successful removal from aqueous solutions to permissible limits. To achieve this aim, the present study investigated, for the first time, the photocatalytical performance of the synthesis FeNi3@SiO2@TiO2 nanoparticles for the HA degradation under different environmental conditions. The photocatalytic reactions were performed using ultraviolet (UV) radiation, whose intensity was fixed at 2500 µW/cm2 throughout the experimental study. The characterization study performed, using specific diagnostic techniques, revealed the presence of several good morphological, magnetic, and catalytic specifications of the synthesized nanoparticles. The use of the simplified form of the Langmuir-Hinshelwood equation sufficiently describes the experimental data of the HA kinetic degradation, as it shows a high coefficient of regression values. Furthermore, the complete HA degradation was reached under conditions of pH = 3; initial HA concentration = 10 mg/L; FeNi3@SiO2@TiO2 nanoparticles dosage = 0.01 g/L; and reaction time >30 min. Thus, the results obtained from this research suggested that the catalyst of FeNi3@SiO2@TiO2 nanoparticles was an attractive, novel, and effective agent, which could be used for the degradation of HA in the photocatalytic processes.

A comparative study of using barberry stem powder and ash as adsorbents for adsorption of humic acid.

In the present research, investigation of the practical utility of barberry stem powder (BSP) and barberry stem ash (BSA) for humic acid (HA) removal from an aqueous medium by adsorption was carried out. The adsorption process was tested by varying of pH (3-11), reaction time (5-20 min), initial HA concentration (5-40 mg/L), adsorbent dosage (1-4 g/L), and temperature (15-35 °C). The isothermal results revealed that the adsorption process is favorable for both used adsorbents and it is highly described using the Freundlich and Langmuir models (R2 > 0.960). Also, the maximum uptakes of BSP and BSA for HA were 20.220 and 16.950 mg/g at the abovementioned optimized conditions (pH = 7, reaction time = 10 min, temperature = 15 °C, initial HA concentration = 40 mg/L, and adsorbent amount = 1.0 g/L), respectively. The results achieved from the fitting of the experimental data with Dubinin-Radushkevich isotherm model showed that the HA molecules are adsorbed onto the BSP and BSA by physiosorption process. From the thermodynamic study, it appeared that the biosorption process of the HA onto two studied adsorbents was of exothermic nature. The kinetics of the adsorption process of HA has been found to be pseudo-second-order model (R2 = 0.930-0.999). Thus, the results obtained from this paper elucidated that the BSP exhibited higher adsorption capacity in comparison to BSA, for HA removal up to permissible concentrations.

Adsorptive performance of a mixture of three nonliving algae classes for nickel remediation in synthesized wastewater.

PURPOSE: The present study provided a comprehensive description regarding the application of a mixture of three nonliving classes of algae as a promising and inexpensive biosorbent for removing toxic nickel (Ni(II)) ions from the aqueous medium. METHODS: The biosorption process was tested by varying several experimental parameters such as pH (2-8), contaminant concentration (20-300 mg/L), biosorbent content (0.2-2 g/100 mL), and temperature (20-40 °C). In addition, the competition effects of the presence of Pb(II), Cu(II), and Zn(II) ions on the Ni(II) removal efficiency was studied by varying their concentrations from 30 to 40 mg/L. RESULTS: The microscopic analysis of algae demonstrated that the used biosorbent consisted mainly of Chrysophyta (80%), Chlorophyte (14%), and Cyanophyta (6%). Results demonstrated that these environmental parameters influenced the removal efficiency with a different degree and there was no stable effects rank at conditions under examination. FT-IR and SEM analysis revealed that the biosorbent surface consists of many strong and active groups of negative valences such as hydroxyl and carboxyl groups, thus exhibiting several morphological properties of interest. Further, it was found that the Temkin model best fitted the isotherm biosorption data. The kinetic study showed that the Ni(II) biosorption was rapid within first 20 min of reaction time, thereby following a pseudo-second-order model, which in turn demonstrated a chemisorption process of Ni(II) ions reaction with the biosorbent binding sites. Also, the thermodynamic study suggested that the biosorption process of Ni(II) onto algal biomass was a spontaneous and endothermic in nature. The maximum uptake of Ni(II) was 9.848 mg/g under optimized conditions and neutral environment. CONCLUSIONS: Thus, this significant finding suggested a favorable and eco-friendly treatment mechanism for removal of Ni(II) ions from aqueous medium via biosorption onto the used mixture of nonliving algal biomass.

Effective reduction of metronidazole over the cryptomelane-type manganese oxide octahedral molecular sieve (K-OMS-2) catalyst: facile synthesis, experimental design and modeling, statistical analysis, and identification of by-products.

High concentrations of antibiotic compounds within pharmaceutical wastewater have hazardous impacts toward environment and human health. Therefore, there is an immediate requirement of efficient treatment method for removal of antibiotics from aquatic environment. In the present study, the cryptomelane catalyst-type manganese oxide octahedral molecular sieve (K-OMS-2) was synthesized in the presence of benzyl alcohol as a reducing agent and cetyltrimethylammonium bromide as a structure-directing agent and then utilized to reduce the metronidazole. The central composite design method was the experimental design adopted. The FESEM analysis revealed that the K-OMS-2 surface contained many uniformly cylindrical aggregates less than about 40 nm in diameter and about 80-100 nm in length. Besides, a high specific surface area of 129 m2/g and average pore size of 45.47 nm were recorded. According to the TGA/DTA analysis, the prepared catalyst revealed high thermal stability. The maximum metronidazole degradation (95.36%) was evident at conditions of pH = 3, catalyst mass = 0.97 g/L, contact time = 200 min, and metronidazole concentration = 20 mg/L. Metronidazole did not form a complex with nitrate, fluoride, sulfate, or hardness. These ions exerted a negligible effect on metronidazole reduction using the K-OMS-2 catalyst, except for hardness, which reduced the removal efficiency of metronidazole by 17%. The FTIR and LC-MS revealed a complex mechanism involved in the metronidazole degradation by the K-OMS-2 involving the formation of an amino group, a hydroxyelated compound via N-denitration, and hydrogenation process on the K-OMS-2 catalyst surface.

Using natural clinoptilolite zeolite as an amendment in vermicomposting of food waste.

The effect of adding different proportions of natural clinoptilolite zeolite (5 and 10%) to food waste vermicomposting was investigated by assessing the physicochemical characteristics, worms' growth, and maturation time of finished vermicompost in comparison with the vermicompost prepared with no amendment (control). Vermicomposting was performed in 18 plastic containers for 70 days. The experimental results showed that the carbon-to-nitrogen (C/N) ratios were 15.85, 10.75, and 8.94 for 5 and 10% zeolite concentration and control after 70 days, respectively. The addition of zeolite could facilitate organic matter degradation and increase the total nitrogen content by adsorption of ammonium ions. Increasing the proportion of zeolite from 0% (control) to 10% decreased the ammonia escape by 25% in the final vermicompost. The natural zeolite significantly reduced the electrical conductivity (EC). At the end of the process, salinity uptake efficiency was 39.23% for 5% zeolite treatment and 45.23% for 10% zeolite treatment. The pH values at 5 and 10% zeolite-amended treatments were 7.31 and 7.57, respectively, in comparison to 7.10 in the control. The maturation time at the end of vermicomposting decreased with increasing zeolite concentration. The vermicompost containing 5 and 10% zeolite matured in 49 and 42 days, respectively, in comparison to 56 days for the control. With the use of an initial ten immature Eisenia fetida worms, the number of mature worms in the 10% zeolite treatment was 26 more than that in the 5% zeolite treatment (21 worms) and 9 more than that in the control treatment (17 worms). Significantly, natural zeolite showed a beneficial effect on the characteristics of the end-product when used in the vermicomposting of food waste.

Brouers-Sotolongo fractal kinetics versus fractional derivative kinetics: A new strategy to analyze the pollutants sorption kinetics in porous materials.

This study presents a detailed comparison of the two most popular fractal theories used in the field of kinetics sorption of pollutants in porous materials: the Brouers-Sotolongo model family of kinetics based on the BurrXII statistical distribution and the fractional kinetics based on the Riemann-Liouville fractional derivative theory. Using the experimental kinetics data of several studies published recently, it can be concluded that, although these two models both yield very similar results, the Brouers-Sotolongo model is easier to use due to its simpler formal expression and because it enjoys all the properties of a well-known family of distribution functions. We use the opportunity of this study to comment on the information, in particular, the sorption strength, the half-life time, and the time dependent rate, which can be drawn from a complete analysis of measured kinetics using a fractal model. This is of importance to characterize and classify sorbent-sorbate couples for practical applications. Finally, a generalization form of the Brouers-Sotolongo equation is presented by introducing a time dependent fractal exponent. This improvement, which has a physical meaning, is necessary in some cases to obtain a good fit of the experimental data.

Optimum efficiency of treatment plants discharging wastewater into river, case study: Tigris river within the Baghdad city in Iraq.

The present study aims to manage and determine the most economical efficiency of five wastewater treatment plants discharging wastewater into the Tigris River in Iraq. The management system was based on ensuring the five-day biological oxygen demand concentration in the river is <30 mg/L according to the Iraqi standards. In many cases, the determined optimized efficiencies were found to be lower than the present working efficiencies. Although this was good for the environment, it was not cost-effective. This study revealed that the variation of river flow rates was not an important factor that effects on the results obtained. It was found that the variation of organic decomposition value in the river and the minimum efficiency limit of the first upstream plant greatly affected the operating efficiency of the downstream plants. Furthermore, no constant rank was recorded for the effects of the natural decomposition on the operating efficiency of each plant. Three points were highlighted from this study: •The optimization methods were used to determine the most economical efficiency of multi wastewater treatment plants.•The effects of the BOD decomposition value, the river flow, and the minimum efficiency limit were also investigated.•This study presents the linear modeling method in detail and has a scientific impact for similar studies.

Enhancement of the adsorption capacity of the light-weight expanded clay aggregate surface for the metronidazole antibiotic by coating with MgO nanoparticles: Studies on the kinetic, isotherm, and effects of environmental parameters.

The synthesized MgO nanoparticles were used to coat the light-weight expanded clay aggregates (LECA) and as a metronidazole (MNZ) adsorbent. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and Fourier-transformed infrared (FTIR) techniques were employed to study the surface morphology and characteristics of the adsorbents. MgO/LECA clearly revealed the advantages of the nanocomposite particles, showing high specific surface area (76.12 m2/g), significant adsorption sites and functional groups. Between pH 5 and 9, the MNZ sorption was not significantly affected. Kinetic studies revealed that the MNZ adsorption closely followed the Avrami model, with no dominant process controlling the sorption rate. The study of the effects of foreign ions revealed that the addition of carbonate raised the MNZ removal efficiency of LECA by 8% and the total removal of MNZ by MgO/LECA. Furthermore, nitrate and hardness only marginally influenced the MNZ removal efficiency and their effects can be ranked in the order of carbonate>nitrate>hardness. The isotherm adsorption of MNZ was best fitted with the Langmuir model enlighten the monolayer MNZ adsorption on the homogeneous LECA and MgO/LECA surfaces. The maximum adsorption capacity under optimum conditions was enhanced from 56.31 to 84.55 mg/g for LECA and MgO/LECA, respectively. These findings demonstrated that the MgO/LECA nanocomposite showed potential as an efficient adsorbent for MNZ removal.

Kinetic modeling of antibiotic adsorption onto different nanomaterials using the Brouers-Sotolongo fractal equation.

In this study, the kinetic data of the adsorption of two antibiotics onto three nanoadsorbents was modeled using the Brouers-Sotolongo fractal model. The model parameters were calculated at different initial antibiotic concentrations using various approximations of the kinetic equation for two quantities of practical relevance: the sorption power and the half-time characteristic of the sorption. The merits of the nanomaterial were then compared in terms of their application in the elimination of dangerous antibiotic wastes. We also developed a formula to calculate the effective rate of the best adsorbent. This study presents the modeling method in detail and has a pedagogical value for similar researches.

Competitive biosorption of lead, cadmium, copper, and arsenic ions using algae.

The present study aims to evaluate the competitive biosorption of lead, cadmium, copper, and arsenic ions by using native algae. A series of experiments were carried out in a batch reactor to obtain equilibrium data for adsorption of single, binary, ternary, and quaternary metal solutions. The biosorption of these metals is based on ion exchange mechanism accompanied by the release of light metals such as calcium, magnesium, and sodium. Experimental parameters such as pH, initial metal concentrations, and temperature were studied. The optimum pH found for removal were 5 for Cd(2+) and As(3+) and 3 and 4 for Pb(2+) and Cu(2+), respectively. Fourier transformation infrared spectroscopy analysis was used to find the effects of functional groups of algae in biosorption process. The results showed that Pb(2+) made a greater change in the functional groups of algal biomass due to high affinity to this metal. An ion exchange model was found suitable for describing the biosorption process. The affinity constants sequence calculated for single system was K Pb > K Cu > K Cd > K As; these values reduced in binary, ternary, and quaternary systems. In addition, the experimental data showed that the biosorption of the four metals fitted well the pseudo-second-order kinetics model.