Synthesis and characterization of Fe3O4@SiO2 -supported metal-organic framework PAEDTC@MIL-101 (Fe) for degradation of chlorpyrifos and diazinon pesticides.

In this study, a new core-shell Fe3O4@SiO2/PAEDTC@MIL-101 (Fe) photocatalyst was prepared by sol-gel method and used to degrade diazinon (DZN) and chlorpyrifos (CPS) from aqueous solutions. The characteristics analyzed by various techniques indicate that the core-shell photocatalyst with a specific surface area of 992 m2/g, pore size of 1.35 nm and saturation magnetization of nanocomposite was 12 emu/g has been successfully synthesized and can be separated from the reaction solution by a magnetic field. The maximum efficiencies of DZN (98.8%) and CPS (99.9%) were provided at pH of 5, photocatalyst dosage of 0.6 g/L, pollutant concentration of 25 mg/L, radiation intensity of 15 W, and time of 60 min. The presence of anions such as sulfate, nitrate, bicarbonate, phosphate, and chloride had a negative effect on the performance of the photocatalysis system. Compared to the adsorption and photolysis systems alone, the photocatalytic process based on Fe3O4@SiO2/PAEDTC@MIL-101 (Fe) under two UV and visible light sources showed a high efficiency of 90% in the reaction time of 60 min. The BOD5/COD ratio improved after 50 min to above 0.4 with TOC and COD removal rates >80%. Scavenging tests showed that •OH radical, hole (h+), electron (e-), and O2•- anion were produced in the reaction reactor, and the •OH radical was the dominant species in the degradation of DZN and CPS. The stability tests confirmed the recyclability of the photocatalyst in 360 min of reactions, with a minimum reduction of 7%. Energy consumption for the present system during different reactions was between 15.61 and 25.06 kWh/m3 for DZN degradation and 10-22.87 kWh/m3 for CPS degradation.

Application of a novel composite of Fe3O4@SiO2/PAEDTC surrounded by MIL-101(Fe) for photocatalytic degradation of penicillin G under visible light.

The novel photocatalyst of Fe3O4@SiO2/PAEDTC@MIL-101(Fe) was prepared based on the sol-gel method, and its structure and morphology were determined by SEM mapping, TEM, XRD, FTIR, and N2 adsorption-desorption analyses. The photocatalytic activity of nanocomposite was evaluated in comparison with other particles as well as adsorption and photolysis processes. The effect of operating parameters showed that the complete degradation of penicillin G (PNG) can be provided at a photocatalyst dosage of 0.6 g/L, radiation intensity of 36 W, pH of 5, and time of 60 min. In the optimum condition, 84% TOC removal was attained and the BOD5/COD rate for the treated effluent was above 0.4, which was representative of the high biodegradability of the treated effluent compared to the raw sample. The findings of energy consumption showed that PNG can be easily and effectively treated by the photocatalytic process based on magnetic MIL-101(Fe) with electrical energy per order between 10 and 20.87 kWh/m3. Due to the excellent interaction between the MIL-101(Fe) and Fe3O4@SiO2/PAEDTC, the photocatalyst stability test showed a recyclability of the particles for 5 consecutive reaction cycles with a minimum reduction of 7%. Solution treated with photocatalyst under UV and visible light sources explained that the toxicity of the effluent after treatment is significantly reduced with the growth of Escherichia coli. Scavenging experiments showed that •OH radical and hole (h+) are the main agents in degrading PNG to CO2, H2O, and biodegradable and low-toxicity products. Finally, the findings of the diagnostic analysis and comparative experiments proved that with the interaction of Fe3O4@SiO2, NH2, and MIL-101(Fe), a lower band gap can be prepared for more absorption of photons and pollutant and also more and faster production of active radicals.

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.

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.

Effective leachate treatment by a pilot-scale submerged electro-membrane bioreactor.

Most landfill leachates contain organic compounds that cannot be easily separated by conventional biological processes. Recently, integration of membrane bioreactors and electro-oxidation has been proposed as a suitable option for the treatment and separation of organic and inorganic contaminants in leachate. Therefore, in the present study, the performance of submerged electro-membrane bioreactor (SEMBR) along with a conventional membrane bioreactor (MBR) on a pilot scale was evaluated for the treatment of leachate. Both bioreactors were used to compare treatment efficiency under the same conditions. The removal rates of chemical oxygen demand (COD), ammonia nitrogen (NH4+-N), phosphate (PO43--P), color, UV254, and metals were investigated. The results showed that applying electric current to the MBR could approximately increase the COD removal efficiency from 94 to 98.5%; PO43--P removal from 70 to 99%; NH3+-N removal from 91 to 99%; UV254 removal from 80 to 96%; and heavy metals removal from 40 to 95%. Humic acid removal efficiency as another indicator of humic substances was increased from 75% in the MBR to 96% in the SEMBR process. The results also showed that the effluent can be introduced into the wastewater treatment plant for further treatment. The SEMBR process achieved a minimization of fouling of membranes compared to conventional MBR. The consumption of the energy and electrode was in accordance with the previous results, and the required energy of 1.57 kWh/m3 of wastewater was calculated. The sludge volume index (SVI) in SEMBR (105 ml/g) was better than MBR (135 ml/g) due to the electrokinetic effect on the production of denser flocs. Based on the results, it can be concluded that the application of electric current can improve the performance of MBR in removing PO43-, NH4+, and membrane fouling.

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.

Evaluation of social accountability in hospital managers.

BACKGROUND: Today, hospitals need managers who, in addition to having the necessary skills for management and leadership, are accountable to stakeholders, especially the community. Accordingly, the purpose of this study was to evaluate the social accountability of managers of public and private hospitals in Tehran. MATERIALS AND METHODS: The present study is descriptive-analytical and cross-sectional and was performed on 155 managers of selected public and private hospitals in Tehran. The research tools included a demographic characteristic questionnaire and a researcher-made social accountability questionnaire for managers. Data analysis was performed using descriptive and inferential statistics in SPSS 22 software. RESULTS: The situation of social accountability in the managers of public hospitals was at a weak level and in the managers of private hospitals in Tehran was at a good level. In comparing the status of social accountability and its dimensions in the managers of public hospitals with the managers of private hospitals, the status of social accountability in the dimensions of human resource management, quality improvement, executive management, and overall social accountability were significantly different from each other (P ≤ 0.05). However, in terms of governance, the status of social accountability of public hospital managers was not significantly different from private hospitals (P ≥ 0.05). Overall, the results of social accountability in private hospitals were better than in public hospitals. CONCLUSION: The social response status of managers in private hospitals was better than public ones. Lack of attention of managers to social accountability affects the quality of other educational, health, and medical services. This fact raises the need for managers to pay more attention to the issue of social accountability.

Magnetic CuNiFe2O4 nanoparticles loaded on multi-walled carbon nanotubes as a novel catalyst for peroxymonosulfate activation and degradation of reactive black 5.

Novel copper-nickel ferrite nanocatalyst loaded on multi-walled carbon nanotube (MWCNTs-CuNiFe2O4) was synthesized and applied to activate peroxymonosulfate (PMS) in the degradation of the reactive black 5 (RB5). The structure of the catalyst was well characterized by scanning electron microscope (SEM), Fourier-transform infrared spectroscopy (FTIR), and X-ray powder diffraction (XRD). The MWCNTs-CuNiFe2O4/PMS system showed a high performance in the degradation of RB5 with a kinetic rate of 1.5-2.5 times higher than homogeneous and heterogeneous systems. Maximum degradation efficiency (99.60%) was obtained at an initial pH of 7, catalyst dosage of 250 mg/L, PMS dosage of 4 mM, the temperature of 25 °C, and reaction time of 15 min. Anion experiments emphasized that the presence of nitrate, carbonate, and phosphate in the solution reduced the degradation efficiency by producing reactive species with low oxidation potential. The RB5 degradation rate evolved with temperature, and the activation energy was obtained to be 44.48 kJ/mol. The mechanism of PMS activation and production of free radicals was proposed based on tert-butyl alcohol (TBA), ethanol (EtOH), and potassium iodide (KI) scavengers. Trapping experiments showed that both sulfate (SO4•-) and hydroxyl (•OH) radicals are involved in the catalytic degradation of RB5. The effective treatment of real wastewater and tap water by the MWCNTs-CuNiFe2O4/PMS system requires a long reaction time. Gas chromatography-mass spectrometry (GC-MS) analysis indicated that RB5 can be degraded via methylation, decarboxylation, hydroxylation, and ring/chain cleavage pathways. The stable catalytic activity after three consecutive cycles suggested that MWCNTs-CuFe2O4 is a novel reusability catalyst in PMS activation.

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.

Photocatalytic degradation of amoxicillin from aqueous solutions by titanium dioxide nanoparticles loaded on graphene oxide.

The photocatalytic degradation of amoxicillin (AMX) by titanium dioxide nanoparticles loaded on graphene oxide (GO/TiO2) was evaluated under UV light. Experimental results showed that key parameters such as initial pH, GO/TiO2 dosage, UV intensity, and initial AMX concentration had a significant effect on AMX degradation. Compared to the photolysis and adsorption processes, the AMX degradation efficiency was obtained to be more than 99% at conditions including pH of 6, the GO/TiO2 dosage of 0.4 g/L, the AMX concentration of 50 mg/L, and the intensity of 36 W. Trapping tests showed that all three hydroxyl radical (OH•), superoxide radical (O2•-), and hole (h+) were produced in the photocatalytic process; however, h+ plays a major role in AMX degradation. Under UV irradiation, GO/TiO2 showed excellent stability and recyclability for 4 consecutive reaction cycles. The analysis of total organic carbon (TOC) suggested that AMX could be well degraded into CO2 and H2O. The formation of NH4+, NO3-, and SO42- as a result of AMX degradation confirmed the good mineralization of AMX in the GO/TiO2/UV process. The toxicity of the inlet and outlet samples of the process has been investigated by cultivation of Escherichia coli and Streptococcus faecalis, and the results showed that the condition is suitable for the growth of organisms. The photocatalytic degradation mechanism was proposed based on trapping and comparative tests. Based on the results, the GO/TiO2/UV process can be considered as a promising technique for AMX degradation due to photocatalyst stability, high mineralization efficiency, and effluent low toxicity.

Catalytic degradation of mefenamic acid by peroxymonosulfate activated with MWCNTs-CoFe2O4: influencing factors, degradation pathway, and comparison of activation processes.

The cobalt ferrite loaded on multi-walled carbon nanotubes (MWCNTs-CoFe2O4) was synthesized and used as a novel catalyst for the degradation of mefenamic acid (MFA) in the presence of peroxymonosulfate (PMS). The results showed that MWCNTs-CoFe2O4 has higher catalytic performance in the activation of PMS and degradation of MFA compared with MWCNTs, Co2+, Fe2+, and CoFe2O4. The highest kinetic constant rate (0.0198 min-1) and MFA degradation (97.63%) were obtained at pH = 7, PMS = 4 mM, catalyst = 500 mg/L, MFA = 10 mg/L, and time = 150 min. MFA degradation accelerated with increasing PMS and catalyst dosage but decreased by initial pH. The influence of different anions and water matrix on the catalytic system was investigated, and the results explained a decrease in the MFA rate in the presence of the interfering substances. Scavenging experiments showed that both sulfate radical anion (SO4•-) and hydroxyl radical (•OH) were effective on MFA degradation, but SO4•- had a greater effect on the degradation of MFA. In addition, the stability and recyclability of MWCNTs-CoFe2O4 were evaluated in the consecutive reaction cycle; the MFA degradation rate reached 89.75% after 4 cycles of reaction. The MFA degradation products were identified by gas chromatography-mass spectrometry (GC-MS) and their degradation pathway was suggested. Finally, a comparison was conducted among the methods used for PMS activation, and the results showed that the cobalt ferrite-based catalyst has high degradation efficiency. However, ultrasound, heat, and ultraviolet (UV) processes can be used to improve the degradation rate of the MWCNTs-CoFe2O4/PMS system at different reaction times.

Multi-walled carbon nanotubes-CoFe2 O4 nanoparticles as a reusable novel peroxymonosulfate activator for degradation of Reactive Black 5.

In this study, CoFe2 O4 nanoparticles supported on multi-walled carbon nanotubes (MWCNTs), as novel peroxymonosulfate (PMS) activator, were synthesized for degradation of Reactive Black 5 (RB5). The results showed that the maximum removal efficiencies of RB5 (100%), chemical oxygen demand (83.12%), and total organic carbon (65.5%) could happen at pH of 7, catalyst dosage of 100 mg/L, PMS dosage of 2 mM, RB5 concentration of 50 mg/L, and time of 30 min. The results of the temperature effect showed that the activation energy (Ea  = 20.92 kJ/mol) for the synthesized catalyst is much lower compared to other studies. The PMS/MWCNTs-CoFe2 O4 system had higher decolorization efficiency and kinetic rates compared to other adsorption and oxidation systems. Quenching experiments proved that RB5 was degraded by sulfate and hydroxyl radicals. The MWCNTs-CoFe2 O4 catalyst showed suitable stability and reusability even after five consecutive catalytic reactions. The continuous treatment of RB5 in real water resources was performed using catalyst packed in a column reactor, and its results showed the high efficiency of the column in the catalytic treatment of the dye at long reaction time. Based on the proposed degradation pathway, the azo bands and the naphthalene structure of RB5 are oxidized to compounds with low molecular weight. PRACTITIONER POINTS: MWCNTs-CoFe2 O4 was used as a novel recyclable catalyst for the activation of peroxymonosulfate and dye degradation. The rate of dye degradation and peroxymonosulfate activation by MWCNTs-CoFe2 O4 was much higher than that of the catalysts alone. Radical SO 4 · - , with contribution percentage of 73.20%, was the main agent for degradation of Reactive Black 5 dye. MWCNTs-CoFe2 O4 in the dye degradation process showed excellent stability and reusability, lower activation energy, and easier separation. The dye degradation products were identified by gas chromatography and UV-vis spectrophotometric analyses, and their degradation pathway was suggested.

Determining the relationship between health literacy level and quality of life among the elderly living in nursing homes.

BACKGROUND: The literacy level of the elderly is predictive of health behaviors, average hospitalization in health centers, and the type of verbal interaction with health service providers; as the level of literacy changes, the quality of life may also change. This study aimed to determine the relationship between health literacy level and quality of life among the elderly living in nursing homes in 2018-2019. MATERIALS AND METHODS: This study was of a descriptive-analytic, correlation type that was performed on 175 elderly of selected nursing homes in Tehran. The research tools included the Abbreviated Mental Test; Control, Autonomy, Pleasure and Self-realization questionnaire-19; and Health Literacy of Iranian Adults Questionnaire (HELIA). Data were analyzed using descriptive and inferential statistics by SPSS 22 software. RESULTS: The total score of health literacy and the quality of life of the elderly was 51.01 and 47.75, respectively. The literacy of most of the studied samples was "inadequate" and "not much adequate" (0-66). The relationship between health literacy and quality of life in the elderly was significant, and there was a direct and statistically significant relationship between them (P = 0.003). That is, by an increase in literacy rates, the scores of quality of life of elderly people were also increased. The correlation was equal to r = -0.28. Health literacy has the ability (31.98%) to predict the quality of life. CONCLUSION: The results showed a lack of enough education literacy, the average quality of life, and the existence of a significant relationship between health literacy and quality of life in the elderly. The wide range of inadequate literacy in the elderly reveals the importance of paying more attention to the issue of literacy in health planning and health promotion at the national and local levels.

Catalytic degradation of diclofenac from aqueous solutions using peroxymonosulfate activated by magnetic MWCNTs-CoFe3O4 nanoparticles.

CoFe3O4 nanoparticles supported on multi-walled carbon nanotubes (MWCNTs-CoFe3O4) were synthesized by the co-precipitation method as a novel catalyst for degradation of diclofenac (DCF). The comparative experiments indicated that MWCNTs-CoFe3O4 has a better catalytic activity in degradation of DCF and activation of peroxymonosulfate (PMS) compared to other catalytic systems. This can be attributed to the interaction of MWCNTs with CoFe3O4 in accelerating the absorption process and activating the PMS (E a = 22.93 kJ mol-1). The removal efficiencies of DCF and total organic carbon (TOC) were 99.04% and 50.11%, under optimum conditions, e.g., pH of 7, PMS dosage of 4 mM, DCF concentration of 30 mg L-1, catalyst dosage of 500 mg L-1, and reaction time of 120 min. The oxidation of DCF was fitted by the pseudo-first-order kinetic model and the constant rate was increased by increasing the pH, temperature, dosage of PMS and catalyst. The production of reactive species was studied using scavengers such as TBA and ethanol and the results showed that sulfate radical is the reactive species responsible for the degradation of DCF. The MWCNTs-CoFe3O4 catalyst showed high stability and reusability based on five successful repeated reactions, X-ray diffraction and energy dispersive X-ray spectroscopy analysis. Based on the intermediates detected by gas chromatography-mass spectrometry (GC-MS), the possible pathways for DCF catalytic oxidation were proposed. The results explained that the PMS/MWCNTs-CoFe3O4 system is a promising method for treating DCF solution due to high efficiency, good reusability of catalyst and greater PMS activation.

Electrochemical degradation of diclofenac using three-dimensional electrode reactor with multi-walled carbon nanotubes.

The electro-oxidation treatment of aqueous solution containing diclofenac (DCF) on a Ti/RuO2-TiO2 electrode in the presence of multi-walled carbon nanotubes (MWCNTs) was studied in a three-dimensional electrochemical (3DE) reactor. The response surface methodology (RSM) based on central composite design (CCD) was utilized to determine the influence of different factors. The results revealed that the obtained polynomial experimental model had a high coefficient of determination (R2 = 0.9762) based on analysis of variance. The optimum condition for the removal of DCF by the 3DE process was obtained with the initial pH of 3.8, the initial DCF concentration of 4 mg/L, the current density of 20 mA/cm2, the particle electrode concentration of 70 mg/L, and the electrolysis time of 85 min. The quadratic model developed for DCF removal and subsequently the analysis of the F value illustrated that the initial pH was the most important factor in the removal of DCF. The comparative experiments between electrochemical processes showed the high electrocatalytic activity and removal efficiency of the 3DE reactor with the MWCNT particle electrode. The results also showed that the Ti/RuO2-TiO2 electrode, in addition to its high stability, had a very good electrocatalytic activity in the 3D reactor. The stability and reusability test proved that MWCNTs, as a particle electrode, had a potential to improve the long-term electrocatalytic degradation of DCF in the aqueous solutions. Based on the identified intermediate compounds along with the results of other studies, a possible pathway for the electrochemical oxidation of DCF by the 3DE process catalyzed with MWCNTs was proposed.