Catalytic electrodes' characterization study serving polluted water treatment: environmental healthcare and ecological risk assessment.

Pesticide residues in the environment have irreparable effects on human health and other organisms. Hence, it is necessary to treat and degrade them from polluted water. In the current work, the electrochemical removal of the fenitrothion (FT), trifluralin (TF), and chlorothalonil (CT) pesticides were performed by catalytic electrode. The characteristics of SnO2-Sb2O3, PbO2, and Bi-PbO2 electrodes were described by FE-SEM and XRD. Dynamic electrochemical techniques including cyclic voltammetry, electrochemical impedance spectroscopy, accelerated life, and linear polarization were employed to investigate the electrochemical performance of fabricated electrodes. Moreover, evaluate the risk of toxic metals release from the catalytic electrode during treatment process was investigated. The maximum degradation efficiency of 99.8, 100, and 100% for FT, TF, and CT was found under the optimal condition of FT, TF, and CT concentration 15.0 mg L-1, pH 7.0, current density 7.0 mA cm-2, and electrolysis time of 120 min. The Bi-PbO2, PbO2, and SnO2-Sb2O3 electrodes revealed the oxygen evolution potential of 2.089, 1.983, 1.914 V, and the service lifetime of 82, 144, and 323 h, respectively. The results showed that after 5.0 h of electrolysis, none of the heavy metals such as Bi, Pb, Sb, Sn, and Ti were detected in the treated solution.

Simultaneous electrochemical degradation of pesticides from the aqueous environment using Ti/SnO2-Sb2O3/PbO2/Bi electrode; process modeling and mechanism insight.

In this work, modified Bi-PbO2 electrode was fabricated and employed for simultaneous degradation of fenitrothion (FT), trifluralin (TF), and chlorothalonil (CT) from synthetic and pesticide wastewater through the anodic oxidation process. A novel high-performance liquid chromatography method was developed and optimized to identify the pesticides simultaneously. Quadratic models were developed to investigate the effects of main operating parameters and predict the degradation efficiencies of the treatment processes. The R2 of the degradation efficiencies were obtained of 0.9847, 0.9910, and 0.9821 for FT, TF, and CT, respectively, which indicates the degree of conformity between the experimental and the actual values of degradation efficiencies, and the adjusted R2 values for the degradation efficiency of FT, TF, and CT in proposed models were 0.9826, 0.9898, and 0.9796, and the values of the predicted R2 were 0.9792, 0.9875, and 0.9755, respectively. The maximum degradation efficiencies of 99.7, 100, and 100% obtained for FT, TF, and CT, respectively, under the optimal operating condition of FT, TF, and CT concentration of 10.0, 6.0, and 8.0 mg L-1, respectively, pH 6.0, the current density 6.0 mA cm-2, and electrolysis time of 60 min. Chemical oxygen demand removal and energy consumption were 64.7% and 5.1 kWh m-3. Eventually, the generated intermediates and other produced species of pesticides through the treatment process was evaluated using a gas chromatography-mass spectrometry method, and their degradation pathways were proposed.

Voltammetric approach for pharmaceutical samples analysis; simultaneous quantitative determination of resorcinol and hydroquinone.

A simple and precise analytical approach developed for single and simultaneous determination of resorcinol (RC) and hydroquinone (HQ) in pharmaceutical samples using carbon paste electrode (CPE) modified with 1-Ethyl-3-methylimidazolium tetrafluoroborate as ionic liquid and ZnFe2O4 nanoparticle. A significant enhancement in the peak current and sensitivity of the proposed sensor observed by using modifiers in the composition of working electrode compared to bare CPE which is in accordance with the results obtained from electrochemical impedance spectroscopy investigations. Electrochemical investigations revealed a well-defined irreversible oxidation peak for RC over a wide concentration range from 3.0 µM to 500 µM in 0.1 M phosphate buffer solution (pH 6.0) with the linear regression equations of Ip (µA) = 0.0276 CRC (µM) + 0.5508 (R2 = 0.997). The limit of detection and quantification for RC analysis were found to be 1.46 µM and 4.88 µM, respectively. However, the obtained SW voltammograms for simultaneous determination of RC and HQ exhibited a desirable peak separation of about 360 mV potential difference and a satisfactory linear response over the range of 50-700 µM and 5-350 µM with the favorable correlation coefficient of 0.991 and 0.995, respectively. The diffusion coefficient (D) of RC and the electron transfer coefficient (α) at the surface of ZnFe2O4/NPs/IL/CPE estimated to be 2.83 × 10- 4 cm s- 1 and 0.76. The proposed sensor as a promising and low-cost method successfully applied for determination of RC in commercial pharmaceutical formulations such as the resorcinol cream of 2% O/W emulsion available on the market with the recovery of 98.47 ± 0.04.

Response surface modeling of ceftriaxone removal from hospital wastewater.

In recent decades, an emerging concern of widespread antimicrobial resistance has been raised due to the existence of pharmaceutical samples such as antibiotics in an aqueous medium. Herein, antibiotic ceftriaxone (CTX) removal from hospital wastewater employing a hybrid process of electrocoagulation (EC) and adsorption (AD) was investigated. The response surface methodology (RSM) was employed to study the influences of main operating variables, including initial CTX concentration, pH, current density, reaction time, and chitosan dosage, on the removal efficiency of the treatment process. Under the optimum condition of the employed EC/AD hybrid treatment process, where initial CTX concentration, pH solution, the current density, adsorbent dosage, and reaction time were set at 20.0 mg L-1, 7.5, 6.0 mA cm-2, 0.75 g L-1, and 12.5 min, respectively, the removal efficiency of 100% was achieved. Analysis of variance (ANOVA) confirmed that the developed quadratic treatment model is highly significant. The applied EC/AD hybrid treatment process revealed the electrical energy consumption of 0.84 kWh m-3 and 0.2168 kWh (g Al)-1 per cubic meter of hospital wastewater and gram of consumed aluminum electrode, respectively. The second-order kinetic model with R2 of 0.9514 and the Langmuir isotherm model with R2 of 0.973 best fit the developed EC/AD hybrid treatment process, and qm was found to be 111.1 mg g-1. The obtained experimental results confirmed that the CTX concentration of the hospital wastewater was reduced to zero after applying the EC/AD hybrid process.

Successful Application of Alpha Lipoic Acid Niosomal Formulation in Cerebral Ischemic Reperfusion Injury in Rat Model.

Purpose: Free radicals such as hydroxyl and peroxide are contributing factors to neuronal destruction in cerebral ischemia. Alpha-lipoic acid (ALA) is one of the potent known antioxidants. Preparation of ALA niosomes allows IV injection and can increase bioavailability and penetration into the central nervous system (CNS). Methods: Film hydration method was used to prepare different niosomes composed of Span®, Tween®, and cholesterol at different molar ratio. ALA and niosome-forming compounds were dissolved in chloroform, before removing the organic solvent by rotary evaporator. Animals were randomly divided into four groups: Sham, control group, intravenous (IV) injection of empty niosomes plus intraperitoneal (IP) injection of ALA solution, and finally, IV injection of ALA niosomes. Rats were subjected to deep anesthesia before inducing cerebral ischemia, then, their internal common carotid arteries were clamped for 15 min and reperfusion was done for 30 min. Niosomal ALA was injected intravenously just before declamping. Results: Mean volume diameter of the prepared niosomes was between 4.36 ± 0.82 and 19.95 ± 1.21 µm in different formulations. Encapsulation efficiency percent (EE%) of ALA in the selected formulation, Span60/Tween60/cholesterol (35:35:30 molar ratio), was 94.5 ± 0.2, and 59.27 ± 5.61% of ALA was released after 4h. In the niosomal group, the rate of reduction in complications of cerebral ischemia such as histopathologic changes and acute damage (from score 3 to 1) in CNS was higher than other groups. Conclusion: The obtained results show that niosomes can be used as effective drug delivery systems for ALA in cerebral ischemia.

Nature-Inspired Effects of Naturally Occurring Trace Element-Doped Hydroxyapatite Combined with Surface Interactions of Mineral-Apatite Single Crystals on Human Fibroblast Behavior.

Innovative engineering design for biologically active hydroxyapatites requires enhancing both mechanical and physical properties, along with biocompatibility, by doping with appropriate chemical elements. Herein, the purpose of this investigation was to evaluate and elucidate the model of naturally occurring hydroxyapatite and the effects of doped trace elements on the function of normal human fibroblasts, representing the main cells of connective tissues. The substrates applied (geological apatites with hexagonal prismatic crystal habit originated from Slyudyanka, Lake Baikal, Russia (GAp) and from Imilchil, The Atlas Mountains, Morocco (YAp)) were prepared from mineral natural apatite with a chemical composition consistent with the building blocks of enamel and enriched with a significant F- content. Materials in the form of powders, extracts and single-crystal plates have been investigated. Moreover, the effects on the function of fibroblasts cultured on the analyzed surfaces in the form of changes in metabolic activity, proliferation and cell morphology were evaluated. Apatite plates were also evaluated for cytotoxicity and immune cell activation capacity. The results suggest that a moderate amount of F- has a positive effect on cell proliferation, whereas an inhibitory effect was attributed to the Cl- concentration. It was found that for (100) GAp plate, fibroblast proliferation was significantly increased, whereas for (001) YAp plate, it was significantly reduced, with no cytotoxic effect and no immune response from macrophages exposed to these materials. The study of the interaction of fibroblasts with apatite crystal surfaces provides a characterization relevant to medical applications and may contribute to the design of biomaterials suitable for medical applications and the evaluation of their bioavailability.

Iron-modified activated carbon derived from agro-waste for enhanced dye removal from aqueous solutions.

BACKGROUND AND AIM: Finding a cost-effective adsorbent can be an obstacle to large-scale applications of adsorption. This study used an efficient activated carbon adsorbent based on agro-waste for dye removal. METHODS: Pistachio shells as abundant local agro-wastes were used to prepare activated carbon. Then, it was modified with iron to improve its characteristics. Acid red 14 was used as a model dye in various conditions of adsorption (AR14 concentration 20-150 mg L-1, pH 3-10, adsorbent dosage 0.1-0.3 g L-1, and contact time 5-60 min). RESULTS: A mesoporous adsorbent was prepared from pistachio shells with 811.57 m2 g-1 surface area and 0.654 cm3 g-1 pore volume. Iron modification enhanced the characteristics of activated carbon (surface area by 33.3% and pore volume by 64.1%). Adsorption experiments showed the high effectiveness of iron-modified activated carbon for AR14 removal (>99%, >516 mg g-1). The adsorption followed the pseudo-second kinetic model (k = 0.0005 g mg-1 min-1) and the Freundlich isotherm model (Kf = 152.87, n = 4.61). Besides, the reaction occurred spontaneously (ΔG0 = -36.65 to -41.12 kJ mol-1) and was exothermic (ΔH0 = -41.86 kJ mol-1 and ΔS0 = -3.34 J mol-1 K-1). CONCLUSION: Iron-modified activated carbon derived from pistachio shells could be cost-effective for the treatment of industrial wastewater containing dyes.

Electro-Fenton approach in oxidative degradation of dimethyl phthalate - The treatment of aqueous leachate from landfills.

Herein, the dimethyl phthalate (DMP) contamination, as an emerging pollutant, has been cost-effectively removed from landfill leachate through an advanced oxidation process, that is the electro-Fenton (EF) process. For this purpose, a quadratic polynomial model was developed via response surface methodology (RSM). Furthermore, the analysis of variance (ANOVA) was performed for evaluating the significance of the proposed assumptions. The actual removal rate of 99.1% was obtained with optimal values of 4 mg L-1 of initial DMP concentration, 50 mM Na2SO4, 600 µL L-1 H2O2, 8-minute electrolytic time, solution pH 3 and 6 mA cm-2 current density for the process variables and was consistent with the expected 99.6% removal rate. Satisfactory correlation coefficients were obtained, and a non-significant value of 0.0618 for model mismatch confirmed that the proposed model is extremely important and can successfully predict the effectiveness of DMP removal. The kinetics of the process and the effect of the presence of some radical scavengers were studied to understand the exact mechanism of DMP degradation. Therefore, it was observed that the reaction of hydroxyl radicals with DMPs followed the first-order kinetics model. Moreover, it was established that the optimal ratio of H2O2/Fe2+ mole was 1.6 and the electricity consumption was 0.157 kWh m-3. The elaborated treatment model used to remove DMP from landfill leachate showed that DMP contamination was effectively removed with a 95.6% removal efficiency in the investigating process.

Adsorption of tetracycline antibiotic onto modified zeolite: Experimental investigation and modeling.

Artificial Neural Networks (ANNs) model and Adaptive Neuro-Fuzzy Inference System (ANFIS) were used to estimate and predict the removal efficiency of tetracycline (TC) using the adsorption process from aqueous solutions. The obtained results demonstrated that the optimum condition for removal efficiency of TC were 1.5 g L-1 modified zeolite (MZ), pH of 8.0, initial TC concentration of 10.0 mg L-1, and reaction time of 60 min. Among the different back-propagation algorithms, the Marquardt-Levenberg learning algorithm was selected for ANN Model. The log sigmoid transfer function (log sig) at the hidden layer with ten neurons in the first layer and a linear transfer function were used for prediction of the removal efficiency. Accordingly, a correlation coefficient, mean square error, and absolute error percentage of 0.9331, 0.0017, and 0.56% were obtained for the total dataset, respectively. The results revealed that the ANN has great performance in predicting the removal efficiency of TC.•ANNs used to estimate and predict tetracycline antibiotic removal using the adsorption process from aqueous solutions.•The model's predictive performance evaluated by MSE, MAPE, and R2.

Potentiometric sensor for iron (III) quantitative determination: experimental and computational approaches.

The current work deals with fabrication and validation of a new highly Fe3+ selective sensor based on benzo-18-crown-6 (b-18C6) using the potentiometric method. The proposed sensor revealed satisfactory performance for quantitative evaluation of Fe3+ trace amount in environmental samples. The ratio of membrane ingredients optimized and the membrane with the composition of 4:30:65.5:0.5 mg of b-18C6:PVC:o-NPOE:KTpClPB exhibited the desirable Nernstian slope of 19.51 ± 0.10 (mV per decade of activity) over the pH range from 2.5 to 5.7 with an acceptable dynamic concentration range of 1.0 × 10-6 M to 1.0 × 10-1 M and lower detection limit of 8.0 × 10-7 M. The proposed sensor demonstrated an appropriate reproducibility with a rapid response time of 12 s and the suitable lifetime of 10 weeks. To validate the accurate response of the proposed sensor, AAS technique applied for the determination of Fe3+ in real aqueous mediums such as drinking tap water and hospital wastewater sample after treatment by electrocoagulation process. Theoretical studies carried out using DFT/B3LYP computational level with 6-311G basis set to optimize the adsorption sites of Fe+3 cationic species by b-18C6. The obtained adsorption energy with large negative value confirmed the formation of a stable complex.

A rapid and efficient removal approach for degradation of metformin in pharmaceutical wastewater using electro-Fenton process; optimization by response surface methodology.

Presence of emerging contaminants such as pharmaceutical products in aquatic environments has received high concern due to their undesirable effect on wildlife and human health. Current work deals with developing a treatment model based on the electro- Fenton (EF) process for efficient removal of metformin (MET) from an aqueous medium. The obtained experimental results revealed that over the reaction time of 10 min and solution pH of 3, the maximum removal efficiency of 98.57% is achieved where the value of MET initial concentration, current density, and H2O2 dosage is set at 10 mg.L-1, 6 mA.cm-2, and 250 µL.L-1, respectively, which is in satisfactory agreement with the predicted removal efficiency of 98.6% with the desirability of 0.99. The presence of radical scavengers throughout the mineralization of MET under the EF process revealed that the generation of •OH radicals, as the main oxidative species, controlled the degradation mechanism. The obtained kinetics data best fitted to the first order kinetic model with the rate constant of 0.4224 min-1 (R2 = 0.9940). The developed treatment process under response surface methodology (RSM) was employed for modeling the obtained experimental data and successfully applied for efficient removal of the MET contaminant from pharmaceutical wastewater as an adequate and cost-effective approach.

Delayed death following paraquat poisoning: three case reports and a literature review.

Paraquat (PQ) poisoning is principally reported in developing countries. However, most fatalities occur elsewhere due to the induction of multi-organ failure. PQ poisoning can hardly be managed by clinical practice, and no specific antidote has come into existence yet. Here three cases, including 17-, 20-, and 23-year-old men, who were poisoned with PQ, have been reported. Furthermore, the literature regarding biological mechanisms, clinical manifestation, and treatment of PQ-induced toxicity was reviewed. Patients who, either intentionally or accidentally, ingested PQ earlier were initially found to be stable at the emergency department (ED). Therefore, they were discharged from the hospital under a follow-up. However, after several days, the patients were referred to the hospital for the second time and despite cardiovascular resuscitation (CPR) efforts, they suddenly expired. The delayed death following exposure to PQ was reported for inducing gradual progressive pulmonary fibrosis, metabolic acidosis, neurotoxicity, renal failure, and liver injury in poisoned patients. Therefore, PQ-intoxicated patients should be supervised for up to several weeks, and kept in the hospital for a longer period of time. Clinical manifestations and laboratory findings are beneficial markers that act as useful predictors of PQ poisoning.

Electrochemical treatment of pharmaceutical wastewater through electrosynthesis of iron hydroxides for practical removal of metronidazole.

Antibiotics as the severe contaminants of aqueous environments were received growing attention during the last decades. The current work is the first report on investigating the potency and efficiency of electrocoagulation process in the successful removal of metronidazole (MNZ) from pharmaceutical wastewater using response surface methodology based on central composite design. The applied method by optimizing the independent and combined effects of significant variables which affecting the EC process enhanced the removal efficiency of MNZ. Analysis of variance was applied to verify the significance of independent variables solely and their interactions. The best removal efficiency of 100% found under the optimal operating condition of initial MNZ concentration 21.6 mg L-1, pH 8.2, current density 6.0 mA cm-2, inter-electrode distance 3 cm, and reaction time of 14.6 min. Isotherm investigations revealed that the Langmuir model with the R2 of 0.994 best fitted to the obtained experimental equilibrium results. The fast adsorption of MNZ on the surface of Fe(OH)3 and [Fe(OH)2]+ with the equilibrium time of 15 min confirmed that the kinetics of the electrocoagulation process follow the pseudo-second-order model (R2 = 0.962). The electrocoagulation process under the optimal operating condition revealed that the electrical energy consumption per each m3 of treated pharmaceutical wastewater, per each g of MNZ, removed, and per each kg of Fe electrode consumed, were found to be 0.516 kWh m-3, 0.0234 kWh g-1, and 0.0436 kWh kg-1, respectively.

In situ generation of hydroxyl radical for efficient degradation of 2,4-dichlorophenol from aqueous solutions.

Since 2,4-dichlorophenol (2,4-DCP) as a priority pollutant is used in numerous industrial processes, its removal from the aqueous environment is of utmost importance and desire. Herein, the authors describe an electrochemical treatment process for efficient removal of 2,4-DCP from aqueous solutions using electro-Fenton (EF) process. Response surface methodology (RSM) was applied to optimize the operating parameters. Analysis of variance (ANOVA) confirmed the significance of the predicted model. The effect of independent variables on the removal of 2,4-DCP was investigated and the best removal efficiency of 98.28% achieved under the optimal experimental condition including initial pH of 3, H2O2 dosage of 80 µL, initial 2,4-DCP concentration of 3.25 mg L-1, current density of 3.32 mA cm-2, and inter-electrode distance of 5.04 cm. The predicted removal efficiency was in satisfactory agreement with the obtained experimental removal efficiency of 99.21%. According to the obtained polynomial model, H2O2 dosage revealed the most significant effect on degradation process. The kinetic investigation revealed that the first-order model with the correlation coefficient of 0.9907 and rate constant (Kapp) of 0.831 min-1 best fitted with the experimental results. Generation of the hydroxyl radicals throughout the EF process controlled the degradation process.

Microniosomes for concurrent doxorubicin and iron oxide nanoparticles loading; preparation, characterization and cytotoxicity studies.

The current work deals with developing a suitable drug delivery system of doxorubicin (DOX) for intraperitoneal chemotherapy using niosomes through formulating non-ionic surfactants consisting of Brij™ 52, span™ 60 and Solulan™ C24. Entrapping the magnetite nanoparticles in the hydrophilic parts of niosomes was accompanied with high-efficient DOX loading by the current novel remote-loading method. Cytotoxicity of the prepared formulations was evaluated in vitro against A549 and PC-12 cell lines using the colorimetric WST-1 assay test. The obtained results revealed that, the cytotoxicity of DOX increased up to 22% especially on A549 cells by the current delivery system.

Titanium (III) cation selective electrode based on synthesized tris(2pyridyl) methylamine ionophore and its application in water samples.

The introduction of low detection limit ion selective electrodes (ISEs) may well pave the way for the determination of trace targets of cationic compounds. This research focuses on the detection of titanium (III) cation using a new PVC-membrane sensor based on synthesized tris(2pyridyl) methylamine (tpm) ionophore. The application and validation of the proposed sensor was done using potentiometric titration, inductively coupled plasma atomic emission spectrometry (ICP-AES), and atomic absorption spectrometry (AAS). The membrane sensor exhibited a Nernstian response to the titanium (III) cation over a concentration range of 1.0 × 10(-6)-1.0 × 10(-2) M and pH range from 1-2.5. The Nernstian slope, the lower of detection (LOD), and the response time (t95%) of the proposed sensor were 29.17 ± 0.24 mV/dec, 7.9 × 10-7 M, and 20 s, respectively. The direct determination of 4-39 µg/ml of titanium (III) standard solution showed an average recovery of 94.60 and a mean relative standard deviation of 1.8 at 100.0 µg/ml. Finally, the utilization of the electrodes as end-point indicators for potentiometric titration with EDTA solutions for titanium (III) sensor was successfully carried out.

Immobilization of ionophore and surface characterization studies of the titanium(III) ion in a PVC-membrane sensor.

Novel ionophores comprising various hydroxide and amine structures were immobilized onto poly(vinyl chloride) (PVC) matrices, and these were examined to determine Ti(III) selectivity. To predict the selectivity of Ti(III), a PVC membrane was used to investigate the binding of Ti(III) to c-methylcalix[4]resorcinarene (CMCR). The study showed that the chelating ligand, CMCR, was coordinated selectively to Ti(III) at eight coordination sites involving the oxygen atoms at the interface of the membrane/solution. The membrane was prepared, based on CMCR as an ionophore, sodium tetrakis(4-fluorophenyl) borate (NaTFPB) as a lipophilic ionic additive, and dioctylphthalate (DOP) as a plasticizer. The immobilization of the ionophore and surface characterization studies revealed that the performance of CMCR-immobilized PVC was equivalent to that of mobile ionophores in supported liquid membranes (SLMs). The strengths of the ion-ionophore (CMCR-Ti(OH)(OH(2))(5) (2+)) interactions and the role of ionophores on membranes were studied via UV-Vis, Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and and X-ray diffraction (XRD).

Immobilization of tris(2 pyridyl) methylamine in a PVC-Membrane Sensor and Characterization of the Membrane Properties.

BACKGROUND: Due to the increasing industrial use of titanium compounds, its determination is the subject of considerable efforts. The ionophore or membrane active recognition is the most important component of any polymeric membrane sensor. The sensor's response depends on the ionophore and bonding between the ionophore and the target ion. Ionophores with molecule-sized dimensions containing cavities or semi-cavities can surround the target ion. The bond between the ionophore and target ion gives different selectivity and sensitivity toward the other ions. Therefore, ionophores with different binding strengths can be used in the sensor. RESULTS: In the present work, poly (vinyl chloride) (PVC) based membrane incorporating tris (2 pyridyl) methylamine (tpm) as an ionophore has been prepared and explored as a titanium(III) selective sensor. CONCLUSIONS: The strengths of the ion-ionophore (Ti(OH)2+-tpm) interactions and the role of ionophore on membrane were tested by various techniques such as elemental analysis, UV-vis, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and powder X-ray diffraction (XRD). All data approved the successful incorporation of organic group via covalent bond.

Thermodynamic study of the complexation of p-isopropylcalix[6]arene with Cs+ cation in dimethylsulfoxide-acetonitrile binary media.

The complexation reactions between the macrocyclic ionophore, p-isopropylcalix[6]arene and Cs+ cation were studied in dimethylsulfoxide-acetonitrile (DMSO-AN) binary non-aqueous solvents at different temperatures using a conductometry method. The conductance data show that the stoichiometry of the (p-isopropylcalix[6]-arene·Cs)+ complex in all binary mixed solvents is 1:1. The stability of the complexes is affected by the composition of the binary solvent media and a non-linear behavior was observed for changes of log K(f) of the complex versus the composition of the binary mixed solvents. The thermodynamic parameters (DH°(c) and DS°(c)) for formation of (p-isopropyl-calix[6]arene·Cs)+ complex were obtained from temperature dependence of the stability constant and the obtained results show that the (p-isopropylcalix[6]arene·Cs)+ complex is enthalpy destabilized, but entropy stabilized, and the values of the mentioned parameters are affected strongly by the nature and composition of the binary mixed solvents.