Article

Application of least squares support vector regression and linear multiple regression for modeling removal of methyl orange onto tin oxide nanoparticles loaded on activated carbon and activated carbon prepared from Pistacia Atlantica wood

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Abstract

Two novel and eco friendly adsorbents namely tin oxide nanoparticles loaded on activated carbon (SnO2-NP-AC) and activated carbon prepared from wood tree Pistacia atlantica (AC-PAW) were used for the rapid removal and fast adsorption of methyl orange (MO) from the aqueous phase. The dependency of MO removal with various adsorption influential parameters was well modeled and optimized using multiple linear regressions (MLR) and least squares support vector regression (LSSVR). The optimal parameters for the LSSVR model were found based on γ value of 0.76 and σ(2) of 0.15. For testing the data set, the mean square error (MSE) values of 0.0010 and the coefficient of determination (R(2)) values of 0.976 were obtained for LSSVR model, and the MSE value of 0.0037 and the R(2) value of 0.897 were obtained for the MLR model. The adsorption equilibrium and kinetic data was found to be well fitted and in good agreement with Langmuir isotherm model and second-order equation and intra-particle diffusion models respectively. The small amount of the proposed SnO2-NP-AC and AC-PAW (0.015g and 0.08g) is applicable for successful rapid removal of methyl orange (>95%). The maximum adsorption capacity for SnO2-NP-AC and AC-PAW was 250mgg(-1) and 125mgg(-1) respectively.

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... However, this method is unable to adequately correlate the effects of the different factors on adsorption process also as their mutual interactions (Tahereh et al. 2014). To rise above this difficulty when studying HA adsorption, statistical tools such as support vector regression (Ghaedi et al. 2016), artificial neural networks (Mohammad Hadi et al. 2018), response surface methodology (RSM) (Jafari et al. 2017) (Mahmood et al. 2019), and principal component analysis (PCA) can be useful. ...
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... performance of the SLR and ANN models [48,49]: ...
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... The study of chemical kinetics can provide important information on adsorption rate and the factors affecting the sorption rate 25 . In order to investigate the mechanism of dye adsorption on MgO, the following models were use. ...
... The study of chemical kinetics can provide important information on adsorption rate and the factors affecting the sorption rate 25 . In order to investigate the mechanism of dye adsorption on MgO, the following models were use. ...
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... The pseudo-first-order rate equation [13] is given by: ...
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... High decolorization of MB and MO by eco-friendly and low-cost chitin and CS-g-PAM adsorbents was due to the presence of chelating groups on chitin and chitosan derivative structures that were responsible for this total removal of two dyes. Data regarding removal of MB and MO by other adsorbents reported in previous study are presented in Table 2 [50][51][52][53][54][55][56][57][58][59]. As shown in Table 2, various materials are used for MB and MO removal: chitin-based materials such as MnO 2 -chitin hybrid, Chitosan/Al 2 O 3 /magnetite nanoparticle composite materials and other different material composites. ...
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New host‐guest supramolecular coordination polymer catalyst 3∞[Co(μ2CN)5(CN)(μ2‐Me3Sn)2(Me3Sn)(H2O)(qox)], SCP1 (qox = quinoxaline) has been synthesized and characterized by single crystal X‐ray diffraction, FT‐IR, UV/Visible and fluorescence spectra, thermal and elemental analyses. The tin atoms act as bridges connecting the Co (CN)6 building blocks. The structure of SCP1 exhibits an unusual self‐coordinated host‐guest 3D network with qox as guest molecule. Also, the nanosized1\ was prepared under ultrasonic irradiation while the morphological features of both were examined by TEM and SEM. SCP1 and nanosized1\ are used as heterogeneous catalysts for removal of toxic dyes under UV and ultrasonic irradiation. The results show high effectively decolorized of indigo carmine dye (IC) without generation of any hazardous wastes or byproducts. The reaction is first order with respect to IC, while the factors affecting the rate constant of the degradation reaction are investigated. Mineralization of IC was investigated by IR and UV spectra. The trapping experiments were carried out to determine the role of active species used for degradation of the dye. The activation parameters of the reaction have been estimated and a possible mechanism of degradation was proposed and discussed in detail. New host‐guest supramolecular coordination polymer catalyst 3∞[Co(µ2CN)5(CN)(μ2‐Me3Sn)2(Me3Sn)(H2O)(qox)], SCP1 (qox = quinoxaline) hasbeen synthesized and characterized. The nanosized1\ are prepared under ultrasonicirradiation and their morphological features were examined. SCP1 and nanosized1\ are used as heterogeneouscatalysts for removal of toxic dyes under UV and ultrasonic irradiation.
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This paper presents a novel method to determine the optimal Multi-layer Perceptron structure using Linear Regression. Starting from clustering the dataset used to train a neural network it is possible to define Multiple Linear Regression models to determine the architecture of a neural network. This method work unsupervised unlike other methods and more flexible with different datasets types. The proposed method adapt to the complexity of training datasets to provide the best results regardless of the size and type of dataset. Clustering algorithm used to impose a specific analysis of data used to train the network such us determining the distance measure, normalization and clustering technique suitable with the type of training dataset used.
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The fabrication of novel functionalized composite materials as adsorbent is considered to be the core research area in adsorption technology for environmental applications. Indiscriminate disposal of industrial effluents containing toxic dyes has become a serious environmental issue across the globe since last few decades. In view of above, this study focused on the performance evaluation of ZnO/polyaniline nanocomposite (ZnO-PANI-NC) for quick ultrasonic assisted adsorptive remediation of methyl orange dye from aqua matrix. ZnO nanoparticles were fabricated by a simple co-precipitation method and ZnO-PANI-NC was synthesized by in situ oxidative polymerization of aniline monomer in presence of ZnO nanoparticles. The nanocomposite was extensively characterized for its crystalline nature, morphological characteristics, surface chemical bonding, specific surface area and pore volume by employing XRD, SEM, TEM, FTIR, and BET analysis. The ZnO-PANI-NC has shown superior adsorptive performance as compared to pure PANI as well as ZnO nanoparticles and the maximum monolayer adsorption capacity of 240.84 mg/g was obtained for the ZnO-PANI-NC. Under ultrasonic environment the adsorption reaction reached to equilibrium (more than 98% MO dye removal) within 15 min of reaction. Adsorption process followed Langmuir isotherm model and second order kinetic model strictly and contribution of intra-particle diffusion was also observed. The ZnO-PANI-NC has shown its high regeneration ability (more than 86%) even after 5th consecutive cycles of adsorption-desorption. Response surface methodology based optimization was used to optimize the adsorption experimental data and maximum MO removal of 99.12% was observed at optimum sonication time 13 min, adsorbent dose 0.38 g/L and initial MO concentration at 28 mg/L.
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Activated carbon was successfully generated from the mixture of corn cob and petai hull which served as adsorbents for Pb (II) ion removal at an aqueous solution. The activation was done using KOH at 800°C carbonization temperature. Synthetic waste used in the various concentration of 100, 200, 300, 400 and 500 ppm. The adsorption process was carried out at 30 minutes, the ratio of adsorbent mass was grouped as B (1:3 corn cob native activated carbon /petai hull native activated carbon ), C (1:1 corn cob native activated carbon /petai hull native activated carbon ), D (3:1, corn cob native activated carbon /petai hull native activated carbon ), and H (1:1, corn cob modifiedactivated carbon /petai hull modifiedactivated carbon ). The results showed that the highest adsorption capacity was found in H adsorbent that was 2,368 mg/g at concentration 300 ppm. Dubinin model fit the adsorption isotherms of B, C, D, and H.
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This study evaluated the feasibility of Rhodamine-B dye (Rh B) removal from aqueous solution, using Lead-Iron Oxide nanoparticles Loaded Activated Carbon (FePbO@AC). The parameters like pH, contact time, adsorbent/adsorbate dosage and temperature on adsorption was studied. Optimized conditions are pH of 7.0, 25 min contact time, 50 ppm of dye concentration and 200 mg of adsorbent concentration. The kinetics of adsorption was calculated using pseudo-first-order, pseudo-second-order, and intra-particle diffusion models. The calculations revealed that the pseudo-second-order kinetic equation best-fit the adsorption data. The Langmuir isotherm model best fit the equilibrium data. The maximum sorption capacity (Qmax) for dye is 1000 mg Rh B/g FePbO@AC. Change in entropy (ΔS), Gibb’s free energy change (ΔG), and enthalpy (ΔH) were calculated for the adsorption of Rh B dye.
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An Ag-MnFe2O4-bentonite composite was synthesized by a chemical co-precipitation method and used for adsorption removal of Pb(II), Cd(II) and disinfection. The result of X-ray diffraction indicate that the diffraction peaks of MnFe2O4 and Ag can be perfectly indexed to the cubic spinel MnFe2O4(JCPDS No.88-1965) and metallic Ag(JCPDS No.41-1402), respectively. The results of scanning electron microscopy and energy dispersive X-ray spectroscopy manifest the deposition of MnFe2O4 and Ag on the bentonite surface and the presence of Mn, Fe and Ag. The result of X-ray photoelectron spectroscopy displayed that the composition of Ag-MnFe2O4-bentonite was Mn(II), Fe(III) and metallic Ag. The analysis of Brunauer-Emmett-Teller showed that the specific surface area of Ag-MnFe2O4-bentonite was the largest compared with that of bentonite, MnFe2O4 and MnFe2O4-bentonite. Thermo-dynamic studies revealed that the adsorption of Pb(II) and Cd(II) ions was spontaneous and endothermic. Langmuir model showed an adsorption capacity of 129.87 mg/g for Pb(II) and 48.31 mg/g for Cd(II) ions. The adsorption ki-netics of Pb(II) and Cd(II) ions onto Ag-MnFe2O4-bentonite can be best described by a pseudo-second-order model. The adsorption rate constant of the pseudo-second-order model was 0.0019 g·mg‒1·min‒1 for Pb(II) and 0.0065 g·mg‒1·min‒1 for Cd(II) ions. In addition to the adsorption experiment, the antibacterial properties of Ag-MnFe2O4-bentonite were studied through plate count method. Gram-negative(G‒) bacteria Escherichia coli and Gram-positive(G+) bacteria Lactobacillus plantarum were used to test the antibacterial properties. The results showed that the composite demonstrated excellent antibacterial activity. Thus, Ag-MnFe2O4-bentonite can be em-ployed as an adsorbent as well as an antimicrobial agent.
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Activated carbon from oak tree is used as adsorbent for the removal of noxious anionic dye sunset yellow. The prepared adsorbent is characterized using X-ray diffraction, Scanning Electron microscopy equipped with Energy-Dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy. In addition to this, parameters like initial concentration, adsorbent dosage, contact time, pH, and particle size on the uptake of SY dye from wastewater is well investigated and optimized. For maximum adsorption, the initial concentration of 10 mg/L; adsorbent dose of 0.25 g; pH =1; contact time = 35 min and particle size = 150–250 μm is found to be optimal value. The adsorption isotherm data at different adsorbent dosage of 0.05–0.25 g is in agreement with the Langmuir isotherm having Qmax = 5.8377–30.1205 mg/g. On the other hand, models like, Group Method of Data Handling and multiple linear regression were used to forecast the removal efficiency of noxious anionic dye sunset yellow and from results, it is specified that the GMDH model possess a high performance than MLR model for forecasting removal percentage of SY dye. Hence, activated carbon from oak tree can be efficiently used as adsorbent for the removal of SY dye from wastewater.
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Chromium is one of the hazardous pollutants in industrial effluents. The aim of this research is to investigate feasibility of using waste eggshells for the removal of Cr(VI) ions from its aqueous solutions. Characterization of crushed and sieved eggshell have been carried out using scanning electron microscope, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray fluorescence, etc. analysis. The effect of pH, Cr(VI) ions concentration, amount of eggshell, contact time, temperature, etc. parameters have been investigated on the adsorption and it has been found that the maximum removal (about 93%) of Cr(VI) onto eggshells can be achieved at 25°C and pH 5 in 90 min. Freundlich and Langmuir adsorption isotherm models e have been verified using experimental data. Results also include calculation of thermodynamic parameters like, change in enthalpy (ΔH 0), change in entropy (ΔS 0), and change in free energy (ΔG 0) of the ongoing adsorption process. Chromium sorption kinetics is also found to be fitted in pseudo-first-order kinetic model. Results clearly indicate that the waste material eggshell, a solid waste from the food industry, can be very effectively used as a sorbent for the removal of chromium ions from its aqueous solutions.
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Textile wastewater presents a challenge to conventional physico-chemical and biological treatment methods. Liquid-phase adsorption has been shown to be highly efficient for the removal of dyes and other organic matters from process or waste effluent. Many different types of adsorbent are used to remove colour from wastewater among which the most widely used material is activated carbon. Since activated carbon is expensive and necessitates regeneration, attempts have been made to substitute alternatives that are biodegradable, low cost and/or waste materials. This article presents the investigations carried out by numerous researchers on the use of different kinds of adsorbents and their adsorption capacities for the removal of specific dyes from textile wastewater.
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In this letter we discuss a least squares version for support vector machine (SVM) classifiers. Due to equality type constraints in the formulation, the solution follows from solving a set of linear equations, instead of quadratic programming for classical SVM''s. The approach is illustrated on a two-spiral benchmark classification problem.
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In this research, activated carbon (AC) simply was prepared from a local, abundant tree in south of Iran. The AC with low cost and toxicity is a good candidate for bromophenol blue (BPB) removal from aqueous media. The AC with nano scale pore diameter is applicable for this dye removal following optimization of the influence of various parameters including contact time, pH, initial dye concentration and amount of adsorbent. Subsequently, experimental data was analyzed by four kinetic models including pseudo first and second-order, Elovich and the intraparticle diffusion equations and subsequently their respective parameters such as rate constants, equilibrium adsorption capacities and correlation coefficients was investigated and based on well known criterion their applicability was judged. The result shows that adsorption of BPB onto proposed adsorbent at all conditions such as versatile adsorbent dosages and initial BPB concentrations sufficiently described by the combination of the pseudo second-order equation and interparticle diffusion model. It was found that equilibrium rate of the BPB adsorption at various adsorbent dosage well fitted by Langmuir. Investigation of experimental result by two approaches (multiple linear regressions (MLR) and random forest (RF)) models show that RF is a powerful tool for prediction of BPB adsorption by activated carbon obtained from Astragalus bisulcatus tree. The optimal tuning parameters for RF model are obtained based on the ntree = 100, mtry = 2. For the training data set, the MSE values of 0.0006 and the coefficient of determination (R2) values of 0.9895 for RF model and the MSE value of 0.0104 and the R2 value of 0.823 for MLR model are obtained.
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The present research is focused on the synthesis and characterization of cobalt (III) oxide (Co2O3) nanoparticle loaded on activated carbon to prepare an outstanding sorbent for the removal of eosin Y (EY) as hazardous dye from aqueous solution. The sorbent was identified by SEM and XRD analysis. The effect of solution pH, adsorbent dosage (0.005–0.02 g), contact time (0.5–30 min) and initial eosin Y concentration (30–80 mg L−1) on the adsorption process was investigated and modeled by artificial neural network. Following optimization of variables, the experimental equilibrium data was analysis by Langmuir, Freundlich, Tempkin and D–R isothermal models and explored that the data well presented by Langmuir model with a maximum adsorption capacity of 555.56 mg g−1 at 25 °C. Kinetic studies at various adsorbent dosage and initial EY concentrations show that high removal percentage (>90%) was achieved within 15 min of the start of every experiment at most conditions. The adsorption of EY follows the pseudo-second-order rate equation in addition to intraparticle diffusion model. The experimental data were applied to train the multilayer feed forward neural network with three inputs and one output with different algorithms and different numbers of neurons in the hidden layer. The minimum mean squared error (MSE) of 1.49e − 04 and determination coefficient of (R2) 0.9991.
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In this research, a novel adsorbent gold nanoparticle loaded on activated carbon (Au-NP-AC) was synthesized by ultrasound energy as a low cost routing protocol. Subsequently, this novel material characterization and identification followed by different techniques such as scanning electron microscope(SEM), Brunauer-Emmett-Teller(BET) and transmission electron microscopy (TEM) analysis. Unique properties such as high BET surface area (>1229.55m(2)/g) and low pore size (<22.46Å) and average particle size lower than 48.8Å in addition to high reactive atoms and the presence of various functional groups make it possible for efficient removal of 1,3,4-thiadiazole-2,5-dithiol (TDDT). Generally, the influence of variables, including the amount of adsorbent, initial pollutant concentration, contact time on pollutants removal percentage has great effect on the removal percentage that their influence was optimized. The optimum parameters for adsorption of 1,3,4-thiadiazole-2, 5-dithiol onto gold nanoparticales-activated carbon were 0.02g adsorbent mass, 10mgL(-1) initial 1,3,4-thiadiazole-2,5-dithiol concentration, 30min contact time and pH 7. The Adaptive neuro-fuzzy inference system (ANFIS), and multiple linear regression (MLR) models, have been applied for prediction of removal of 1,3,4-thiadiazole-2,5-dithiol using gold nanoparticales-activated carbon (Au-NP-AC) in a batch study. The input data are included adsorbent dosage (g), contact time (min) and pollutant concentration (mg/l). The coefficient of determination (R(2)) and mean squared error (MSE) for the training data set of optimal ANFIS model were achieved to be 0.9951 and 0.00017, respectively. These results show that ANFIS model is capable of predicting adsorption of 1,3,4-thiadiazole-2,5-dithiol using Au-NP-AC with high accuracy in an easy, rapid and cost effective way.
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In this paper, we propose a LSSVR-based time series method (LTSM) to predict dynamic lateral deformation of retaining structure and ground surface settlement in deep foundation pit engineering. After reconstructing phase space, time-varying lateral displacement of each observation point on retaining structure can be predicted using its historic unary time series data. And then, the ground settlement nearby the deep foundation pit can be predicted using all the observed values of lateral deformation which were collected at the same time from different depths on the retaining structure. The experimental results show that LTSM achieved a high accuracy when predicting the lateral deformation and ground settlement.
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This work devoted to the investigation of adsorption of reactive orange 12 (RO-12) by gold nanoparticles loaded with activated carbon (Au-NP-AC), which in high efficiency by routine manner was synthesized in our laboratory. Generally, in batch adsorption procedure, the effect of variables, including adsorbent mass, initial RO-12 concentration, and contact time on its removal percentage was optimized by the application of artificial neural networks and based on an imperialist competitive algorithm. This novel adsorbent by small amount (0.02 g) really is applicable to the removal of the high amount of dye (RO 12) in a short time (<20 min). The optimum variables for adsorption of RO 12 onto gold nanoparticle-activated carbon were 0.02 g adsorbent mass, 10 mg L-1 initial RO-12 concentration, 20 min contact time and pH 1. The kinetic of proposed adsorption processes efficiently followed, pseudo-second-order and intra-particle diffusion kinetic models. The equilibrium data of the removal process strongly follow the Langmuir monolayer adsorption with high adsorption capacity. The adsorption capacity of Au-NP-AC for the removal of RO-12 was found to be 714.3 mg g(-1). The comparison of the results obtained using the proposed models showed that the ANN model is better than the MLR model for the prediction of reactive orange 12 adsorption onto gold nanoparticles loaded on activated carbon. The coefficient of determination (R-2) and mean squared error (MSE) for the optimal ANN model with 9 neurons at hidden layer were obtained to be 0.9720 and 0.0007, respectively.
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In this work Tin oxide nanoparticles were synthesized and loaded on activated carbon (SnO2–NP–AC). Prepared SnO2–NP–AC was used as an adsorbent for the removal of Malachite green-oxalate from aqueous medium. The morphological properties of the prepared adsorbent were investigated by using X-ray diffraction (XRD), scanning electron microscope (SEM) and BET analysis. The removal percentage in batch mode was investigated at various operating parameters like; initial pH, contact time, amount of adsorbents and initial dye concentration. The experimental equilibrium data were analyzed by using various models and it was seen that Langmuir isotherm model fitted well with maximum monolayer adsorption capacity of 142.87 mg g− 1. The adsorption kinetic data followed both pseudo second-order kinetics and intraparticle diffusion mechanism.
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An agricultural waste-orange peel powder (OPP) was successfully modified into a novel magnetic nano-adsorbent (MNP–OPP) by co-precipitating it with Fe3O4 nanoparticles (MNP) for cadmium ion removal from aqueous solutions. Characterization of MNP–OPP by FTIR, SEM, XRD, TEM and VSM revealed the covalent binding of hydroxyl groups of MNP with the carboxyl groups of OPP, and further confirmed its physico-chemical properties favorable for metal binding. The cadmium adsorption onto MNP–OPP, MNP and OPP was tested under different pH, ionic strength, natural organic matter, adsorbate concentration, contact time and temperature conditions. Results revealed a faster kinetics and efficiency of MNP–OPP in comparison to those of MNP and OPP and further confirmed a complexation and ion exchange mechanism to be operative in metal binding. The adsorption equilibrium data obeyed the Langmuir model and the kinetic data were well described by the pseudo-second-order model. Thermodynamic studies revealed the feasibility and endothermic nature of the system. Breakthrough capacity from column experiments, adequate desorption as well as reusability without significant loss of efficiency established the practicality of the developed system. Cadmium removal was achieved at 82% from a simulated electroplating industry wastewater. The experimental results reveal the technical feasibility of MNP–OPP, its easy synthesis, recovery, economic, eco-friendly and a promising advanced adsorbent in environmental pollution cleanup.
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The CdSe nanoneedles were successfully grown by a green room temperature solution method. The preparation conditions induce a unilateral growth from base to tip of nanoneedle-like structures, despite the absence of any template. X-ray diffraction and scanning electron microscopy show that the CdSe nanoneedles crystallize in the wurtzite-structure with the growth direction along . A photoluminescence peak with full width at half maximum of around 30nm could be obtained, which indicates a homogeneous and narrow size distribution for the CdSe nanoneedles.
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The voltammetric oxidation of paracetamol on single-walled carbon nanotubes (SWNT) modified edge plane pyrolytic graphite electrode (EPPGE) was explored in phosphate buffer solution by using square wave voltammetry. Cyclic and square wave voltammetry studies indicated the oxidation of paracetamol at the electrode surface through a two-electron reversible step and fundamentally controlled by adsorption. Besides semi-infinite planar diffusion, the role of thin layer diffusion at nanotube modified electrodes is also suggested. The sensitivity at SWNT modified EPPGE is ∼2 times more than that at MWNT modified EPPGE. Paracetamol gave a sensitive oxidation peak at ∼187mV at pH 7.2 (μ=0.5M) which was used to quantitate the drug in the range of 5–1000nM with a detection limit of 2.9×10−9M at SWNT modified EPPGE. The interfering effect of physiologically common interferents on the current response of paracetamol has been reported. The procedure was successfully applied for the assay of paracetamol in pharmaceutical formulations. The applicability of the developed method to determine the drug in human urine samples obtained after 4h of administration of paracetamol is illustrated.
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The effluent from dye manufacturing plant is generally recalcitrant to be decolourized visibly because of versatile composition resulting environmental problem. Hence, the UV/H2O2 process conducted using the recirculated batch reactor system with four annular UV lamps was proposed to treat the dye plant effluent in this work, while identifying the effects of hydrogen peroxide dosage, UV power input and wastewater strength on the decolouration and COD removal. From the experimental results, substantial decolouration and COD removal was increased significantly by supplementing hydrogen peroxide dosage, UV power input. Moreover, the pseudo-first order model was developed to describe the decolouration behaviour that the kinetic rates were calculated by linear regression obtaining the decolouration rate constant of 0.0993mins−1 while 72.0Wl−1 of UV power and 116.35mM of H2O2 dosage for 10% diluted plant wastewater with PtCo colour of 4550 units and COD of 1065mgl−1. Ultimately, the proposed recirculated four-lamp annular UV/H2O2 reactor conducted profitably to not only decolourize but also mineralize the dye plant effluent at the same time.
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5,7,12,14-Tetramethyldibenzotetraazaannulene (Me4Bzo2TAA) has been explored as an electroactive material for preparing poly(vinyl chloride) (PVC)-based membrane electrodes selective to Ni2+. The membrane having the constituents Me4Bzo2TAA, sodium tetraphenyl borate (NaTPB) and PVC in the optimum ratio 2:1:97 (w/w) gave the best working concentration range (7.9×10−6–1.0×10−1M) with a Nernstian slope (30.0+−1.0mV/decade of activity) in the pH range 2.7–7.6. The sensor exhibits a fast response time of 15s. The electrode shows good selectivity for nickel(II) over a number of mono-, bi- and tri-valent cations. Analytical application of the electrode has been investigated for the quantitative determination of Ni2+ in chocolates and the sensor has been successfully used as an indicator electrode in the potentiometric titration of Ni2+ against EDTA.
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writes that the use of neonicotinoid insecticides has been tl y restricted because of their fects on pollinators. Neonicotinoid to v er tebrates due to their high to xicity , en vironmental persistence, w ater solubility , and poten tial
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Polyamine flocculants were synthesized and applied for the removal of color, turbidity, and organic compounds from dye wastewater. The effect of polyamine on color removal was investigated by comparing 2 treatments: 1) alum alone and 2) alum/polyamine in combination. The effects of polyamine flocculant, concentration, types, and pH on the removal efficiency of colored materials were investigated. Polyamine flocculants were highly efficient in the removal of color and turbidity from dye wastewater. Compared with alum alone treatment, an addition of 25 mg/L of polyamine could reduce alum dosage by more than 50% and improve the color and turbidity removal efficiency. Highly efficient color removal was obtained by adding polyamine as a flocculant at widely different pH ranges. Results indicate that the use of polyamine flocculant is cost effective in dye wastewater treatment because it minimizes the amount of sludge produced as the dosage of inorganic coagulant is highly reduced. Effects of zeta potential and pH are also discussed in the paper.
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An overview of potentiometric sensors that are capable of detecting toxic heavy metal ions in environmental samples is presented and discussed. Notwithstanding the tremendous work performed so far, it is obvious that still several limitations do exist in terms of selectivity, limits of detection, dynamic ranges, applicability to specific problems, and reversibility. A survey on important advances in potentiometric sensors with regard to high selectivity, lower detection limit, fast response time, and on-line environmental analysis is presented in this review article.[Supplemental materials are available for this article. Go to the publisher's online edition of Critical Reviews in Analytical Chemistry to view the free supplemental file.]
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The removal of the dye—tartrazine by photodegradation has been investigated using titanium dioxide surface as photocatalyst under UV light. The process was carried out at different pH, catalyst dose, dye concentration and effects of the electron acceptor H2O2. It was found that under the influence of TiO2 as catalyst, the colored solution of the dye became colorless and the process followed a pseudo first order kinetics. The optimum conditions for the degradation of dye were 6 × 10− 5 M dye concentration, pH of 11, and 0.18 mg/L of catalyst dose. In order to evaluate the effect of electron acceptor, the effect of H2O2 on the degradation process was also monitored and it was found that the hydroxyl radical formation and retardation of electron–hole recombination took place simultaneously. The adsorption studies of tartrazine at various dose of TiO2 followed the Langmuir isotherm trend. In order to determine the quality of waste water, Chemical Oxygen Demand (COD) measurements were carried out both before and after the treatment and a significant decrease in the values was observed, implying good potential of this technique to remove tartrazine dye from aqueous solutions.Graphical abstractResearch highlights►Degradation efficiency increases with increase in catalyst concentration. ►Adsorption of tartrazine on TiO2 followed the Langmuir isotherm. ►The photocatalytic kinetics follows first order.
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Activated carbon, developed from fertilizer waste, has been used for the removal of Hg2+, Cr6+, Pb2+, and Cu2+. Mass transfer kinetic approach has been successfully applied for the determination of various parameters necessary for designing a fixed-bed absorber. Parameters selected are the length of the (PAZ) primary adsorption zone (δ), total time involved for the establishment of primary adsorption zone (tx), mass rate of flow to the absorber (Fm), time for primary adsorption zone to move down its length (tδ), amount of adsorbate adsorbed in PAZ from breakpoint to exhaustion (Ms), fractional capacity (f), time of initial formation of PAZ (tf) and per cent saturation of column at break point. Chemical regeneration has been achieved with 1 M HNO3.
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The sorption of three disperse dyes, namely, Disperse Blue 56 (DB56), Disperse Red 74 (DR74) and Disperse Yellow 119 (DY119), onto alunite has been studied in terms of pseudo-first- and second-order sorptions and intraparticle diffusion processes thus comparing chemical sorption and diffusion sorption processes. The pseudo-second-order model provided a high degree of correlation with the experimental data for the sorption processes. There was a small discrepancy at the beginning of the experiments (5–30 min) which suggested that intraparticle diffusion may be involved up to 30 min of the sorption process. The kinetics of sorption, based on the sorption capacities of disperse dyes on alunite, were followed at various time intervals. Results show that the intraparticle diffusion may be rate-limiting, followed by the pseudo-second-order kinetic model in the sorption of disperse dyes onto alunite during agitated batch contact time experiments. The rate constant, the equilibrium sorption capacity and the initial sorption rate were calculated as a function of the effect of alunite particle size, alunite dose, initial dye concentration and pH of the solution.
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This work concerns the treatment of textile plant effluent after conventional biological processing. The objective was a feasibility study of the combination of physicochemical treatment with nanofiltration (NF) and/or reverse osmosis (RO) for water reuse. In fact, dead-end filtration by microfiltration (MF), ultrafiltration (UF), NF and RO tests showed that a primary physicochemical treatment (coagulation/flocculation) was necessary to limit membrane fouling. Two coagulants (organic polyelectrolyte and/or ferric chloride) were tested and compared by carrying out jar-tests using different chemical concentrations at pH 6.8. Then, NF and/or RO experiments were performed and investigated at different operating pressures. Results showed that NF allowed the higher flow rate, 90 L.h−1.m−2 at 18.5 bar transmembrane pressure. Moreover, the permeate quality obtained in this condition was similar to the RO. Conductivity, absorbance at 490 nm and the dissolved organic carbon value of the NF permeates were lower than 390 μS.cm−1, 0 and 2 mg.L−1 of C, respectively. The percent production rate increased with the transmembrane pressure. NF performed at 18.5 bar transmembrane pressure allowed a higher yield (22.6%) than RO (18.3%).
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The filtration of wastewaters generated in the cork industrial process is investigated by using three membranes in tangential filtration laboratory equipment. The three membranes used were two microfiltration membranes with pores sizes of 0.65 and 0.1 μm (DUR-0.65 and DUR-0.1 membranes), and a ultrafiltration membrane with a molecular weight cut-off of 300 kDa (BIO-300K membrane). The water hydraulic permeability was determined for each membrane (values of 860, 248 and 769 L h−1 m−2 bar−1 were found), and the influence on the permeate flux of the main operating variables, such as transmembrane pressure, feed flow rate, temperature and nature of the membranes, was established. The effectiveness of the different membranes and operating conditions was evaluated by determining the removal obtained for several parameters which measure the global pollutant content of the effluent: COD, absorbance at 254 nm, tannic content, color and ellagic acid, which is selected as a major model pollutant among the different organic compounds present in this wastewater. The values of the corresponding retention coefficients depended on the operating conditions, but in all cases were in the sequence: ellagic acid and color > absorbance at 254 nm > tannic content > COD. Globally, the higher removals were obtained for the BIO-300K membrane at 20 °C, with QF = 5.3 L h−1 and TMP = 1.8 bar. Finally, the fouling of the membranes was assessed, and the corresponding mechanism for each membrane was established by fitting the experimental data to various filtration fouling models reported in the literature.
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Textile dyeing processes are among the most environmentally unfriendly industrial processes, because they produce coloured wastewaters that are heavily polluted with dyes, textile auxiliaries and chemicals. The coagulation/flocculation method was studied as a wastewater treatment technique for the decolourization of residual dyebath effluents after dyeing cotton/polyamide blends using reactive and acid dyes. It was discovered that a combination of aluminium sulphate and a cationic organic flocculant yields an effective treatment for residual dyebath wastewaters since almost complete decolourization was achieved, TOC, COD, AOX, BOD and the anionic surfactants were reduced and the biodegradability was increased.
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The high rate of electron/hole pair recombination reduces the quantum yield of the processes with TiO(2) and represents its major drawback. Adding a co-adsorbent increases the photocatalytic efficiency of TiO(2). In order to hybridize the photocatalytic activity of TiO(2) with the adsorptivity of carbon nanotube, a composite of multi-walled carbon nanotubes and titanium dioxide (MWCNT/TiO(2)) has been synthesized. The composite was characterized by means of X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), Fourier transform infrared absorption spectroscopy (FTIR), and diffuse reflectance UV-vis spectroscopy. The catalytic activity of this composite material was investigated by application of the composite for the degradation of methyl orange. It was observed that the composite exhibits enhanced photocatalytic activity compared with TiO(2). The enhancement in photocatalytic performance of the MWCNT/TiO(2) composite is explained in terms of recombination of photogenerated electron-hole pairs. In addition, MWCNT acts as a dispersing agent preventing TiO(2) from agglomerating activity during the catalytic process, providing a high catalytically active surface area. This work adds to the global discussion of how CNTs can enhance the efficiency of catalysts.
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In this study, an evolving least squares support vector machine (LSSVM) learning paradigm with a mixed kernel is proposed to explore stock market trends. In the proposed learning paradigm, a genetic algorithm (GA), one of the most popular evolutionary algorithms (EAs), is first used to select input features for LSSVM learning, i.e., evolution of input features. Then another GA is used for parameters optimization of LSSVM, i.e., evolution of algorithmic parameters. Finally, the evolving LSSVM learning paradigm with best feature subset, optimal parameters and a mixed kernel is used to predict stock market movement direction in terms of historical data series. For illustration and evaluation purposes, three important stock indices, S&P 500 Index, Dow Jones Industrial Average Index, and New York Stock Exchange Index, are used as testing targets. Experimental results obtained reveal that the proposed evolving LSSVM can produce some forecasting models that are easier to be interpreted by using a small number of predictive features and are more efficient than other parameter optimization methods. Furthermore, the produced forecasting model can significantly outperform other forecasting
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In this study, a zirconium nanoparticle sorbent for significantly enhanced adsorption of arsenate (As(V)) was successfully synthesized. The characterization of the zirconium nanoparticle sorbent and its adsorption behavior for arsenate were investigated. The HRTEM micrographs showed that the sorbent was nanoscale with particle sizes ranging from 60 to 90nm. The thermal gravimetric and elemental analyses indicated that the sorbent had a molecular formula of Zr(2)(OH)(6)SO(4)·3H(2)O. The X-ray diffraction study revealed that the sorbent was amorphous. The potentiometric titration study demonstrated the surface charge density of the sorbent decreased with an increase in solution pH, and the pH of zero point charge of the sorbent was around 2.85. The kinetics study showed that most of the uptake took place in the first 6h, and the adsorption equilibrium was obtained within 12h. The optimal pH for As(V) adsorption was between 2.5 and 3.5. The Langmuir equation well described the adsorption isotherm; the maximum adsorption capacity of 256.4mg As/g was found at the optimal pH, better than most of sorbents available in the market. The presence of fluoride or nitrate did not obviously affect the adsorption of As(V) onto the sorbent; however, the existence of humic acid, phosphate or silicate in aqueous solution significantly reduced the uptake of As(V). The humic acid did not cause the reduction of the As(V). The FTIR and XPS spectroscopic analyses revealed that surface hydroxyl and sulfur-containing groups played important roles in the adsorption.
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In this article a super selectivity potentiometric methodology, using an ion-selective electrode, for determination of mercury ion(II) in aqueous solution was investigated. For modification of the electrode a room temperature ionic liquid, 1-n-butyl-3-methylimidazolium tetrafluoroborate (BMIM·BF(4)), was applied as a super conductive binder, and Multi-walled carbon nanotubes (MWCNTs) was used in the composition of the carbon paste to improve conductivity and transduction of chemical signal to electrical signal. Moreover, incorporation of 1-(2-ethoxyphenyl)-3-(3-nitrophenyl)triazene (ENTZ) as an ionophore to this composition caused to significantly enhanced selectivity toward Hg(II) ions over a wide concentration range of 1.0×10(-4) to 5.0×10(-9) M with a lower detection limit of 2.5×10(-9) M (0.5 ppb) and a Nernstian slope of 29.3±(0.2) mV decade(-1) of Hg(II) activity. The electrode has a short response time (∼5s) and can be used for at least 55 days without any considerable divergence in potentials, and the working pH range was 2.0-4.3. Finally, the proposed electrode was successfully used as an indicator for potentiometric determination of Hg(II) in dental amalgam and water samples.
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Al(3+) selective sensor has been fabricated from poly(vinyl chloride) (PVC) matrix membranes containing neutral carrier morin as ionophore. Best performance was exhibited by the membrane having composition as morin:PVC:sodium tetraphenyl borate:tri-n-butylphosphate in the ratio 5:150:5:150 (w/w, mg). This membrane worked well over a wide activity range of 5.0x10(-7) to 1.0x10(-1)M of Al(3+) with a Nernstian slope of 19.7+/-0.1mV/decade of Al(3+) activity and a limit of detection 3.2x10(-7)M. The response time of the sensor is approximately 5s and membrane could be used over a period of 2 months with good reproducibility. The proposed sensor works well over a pH range (3.5-5.0) and demonstrates good discriminating power over a number of mono-, di- and trivalent cations. The sensor can also be used in partially non-aqueous media having up to 20% (v/v) methanol, ethanol or acetone content with no significant change in the value of slope or working activity range. The sensor has also been used in the potentiometric titration of Al(3+) with EDTA and for its determination in zinc plating mud and red mud.
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A mu-bis(tridentate) ligand named 2-phenyl-1,3-bis[3'-aza-4'-(2'-hydroxyphenyl)-prop-4-en-1'-yl]-1,3-imidazolidine (I) has been synthesized and scrutinized to develop iron(III)-selective sensors. The addition of sodium tetraphenyl borate and various plasticizers, viz., chloronaphthalene, dioctylphthalate, o-nitrophenyl octyl ether and dibutylphthalate has been used to substantially improve the performance of the sensors. The membranes of various compositions of the ligand were investigated and it was found that the best performance was obtained for the membrane of composition (I) (10mg):PVC (150mg):chloronaphthalene (200mg):sodium tetraphenyl borate (9mg). The sensor showed a linear potential response to iron(III) over wide concentration range 6.3x10(-6) to 1.0x10(-1)M (detection limit 5.0x10(-6)M) with Nernstian slope (20.0mV/decade of activity) between pH 3.5 and 5.5 with a quick response time of 15s. The potentiometric selectivity coefficient values as determined by match potential method (MPM) indicate excellent selectivity for Fe(3+) ions over interfering cations. The sensor exhibits adequate life of 2 months with good reproducibility. The sensor could be used in direct potentiometry.
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SnO2 quantum dots (QDs) and ultrathin nanowires (NWs) with diameters of approximately 0.5-2.5 and approximately 1.5-4.5 nm, respectively, were controllably synthesized in a simple solution system. They are supposed to be ideal models for studying the continuous evolution of the quantum-confinement effect in SnO2 1D --> 0D systems. The observed transition from strong to weak quantum confinement in SnO2 QDs and ultrathin NWs is interpreted through the use of the Brus effective-mass approximation and the Nosaka finite-depth well model. Photoluminescence properties that were coinfluenced by size effects, defects (oxygen vacancies), and surface capping are discussed in detail. With the SnO2 QDs as building blocks, various 2D porous structures with ordered hexagonal, distorted hexagonal, and square patterns were prepared on silicon-wafer surfaces and exhibited optical features of 2D photonic crystals and enhanced gas sensitivity.
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This paper describes the use of photo-fenton process for color removal from textile wastewater stream. The wastewater sample to be treated was simulated by using colorless polyvinyl alcohol (PVA) and reactive dyestuff of R94H. As a result, the hydroxyl radical (HO*) oxidation can effectively remove color, but the chemical oxygen demand (COD) was removed in a slight degree. The color removal is markedly related with the amount of HO* formed. The optimum pH for both the OH* formation and color removal occurs at pH 3-5. Up to 96% of color can be removed within 30 min under the studied conditions. Due to the photoreduction of ferric ion into ferrous ion, color resurgence was observed after 30 min. The ferrous dosage and UV power affect the color removal in a positive way, however, the marginal benefit is less significant in the higher range of both. PVA as the major background COD of a textile wastewater stream inhibits the color removal insignificantly as its concentration increases.