Selective biosorption mechanism of methylene blue by a novel and reusable sugar beet pulp cellulose/sodium alginate/iron hydroxide composite hydrogel.

A cellulose-based sodium alginate/iron hydroxide (C/SA/Fe) composite hydrogel was fabricated by using epichlorohydrin as cross-linking agent as an effective adsorbent for dye. The physicochemical structure of the C/SA/Fe hydrogel was characterized by SEM, FTIR, XRD and TG. The adsorption performance for the removal of methylene blue (MB) was investigated. In addition, the selective adsorption of cationic dye was also studied. The FTIR analysis revealed that the Fe(OH)3 colloidal particles were successfully combined in the cellulose/sodium alginate hydrogel. The modified hydrogel had better adsorption performance, and the maximum adsorption capacity of C/SA/Fe0.5 for MB was 105.93 mg/g according to the fitting results of adsorption isotherm. The kinetic study showed that the adsorption of MB onto C/SA/Fe was more consistent with the pseudo-second-order model, and was dominated by chemisorption mechanism such as ion exchange or electron sharing. The adsorption data fits well with the Langmuir model. Thermodynamics analysis showed that the MB adsorption by C/SA/Fe was exothermic, spontaneous, favorable and feasible. After five adsorption-desorption cycles, the adsorption capacity was almost unchanged. So, the C/SA/Fe hydrogel is a potential material in the field of the recovery of agricultural by-products or other bio-based cellulose, or environmental protection, etc.

Large-scale converting waste coffee grounds into functional carbon materials as high-efficient adsorbent for organic dyes.

Functional carbon materials have been fabricated through simple and effective catalytic carbonization with waste coffee grounds (CGs) as carbon precursor and FeCl3 as catalyst. The effect of FeCl3 loading and carbonization temperature on carbon yield was investigated. The morphology and structure of as-synthesized carbons was characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and nitrogen isothermal adsorption/desorption measurement, respectively. Furthermore, the carbon materials showed high efficiency for the removal of methylene blue (MB, 653.6 mg g-1), methyl orange (MO, 465.8 mg g-1) and rhodamine B (RB, 366.1 mg g-1). More importantly, the carbon was magnetic, so it can be easily separated by a magnet and reused multiple times. This work not only exploited a low-cost and large-scale preparation method to synthesize functional carbon materials from bioresources, but also provided an eco-friendly and effective adsorbent in water purification applications.

Populus tremula, Nerium oleander and Pergularia tomentosa seed fibers as sources of cellulose and lignin for the bio-sorption of methylene blue.

Cellulose-based substrates could represent potential funds for the sorption of pollutants. Herein, methylene blue was selected for demonstrating the bio-sorption efficiency of Nerium oleander, Pergularia tomentosa and Populus tremula seed fibers. Their cellulose contents were 45%, 43.8% and 60%. Their lignin amounts were 21%, 8.6% and 12%, respectively. Fourier Transform InfraRed suggested that the interaction of these bio-products with methylene blue could occur between hydroxyl and ester groups of cellulose and lignin and the sulfur and nitrogen atoms of the dye. Scanning Electron Microscopy showed a swelling of the bio-matters after dye biosorption. From X-Ray Diffraction, the shifting for higher values of the peaks related to the amorphous phase indicated the establishment of new rearranged regions. Such change from the decomposition behavior event studied by Thermogravimetric Analysis/Differential Thermal Analysis revealed that methylene blue was interacted with cellulose and lignin structures. The effect of adsorbent dosage, pH, time, dye concentration and temperature was investigated in controlled batch experiments. Excellent sorption capacities followed the order: Nerium oleander (280.2 mg g-1) > Populus tremula (168 mg g-1) > Pergularia tomentosa (145.3 mg g-1). Freundlich fitted best the equilibrium data suggesting cooperative interactions via physisorption and chemisorption phenomenon. Kinetic data complied well with the pseudo-second-order suggesting a chemisorption mechanism.

Methylene blue removal by using pectin-based hydrogels extracted from dragon fruit peel waste using gamma and microwave radiation polymerization techniques.

This research aims to compare the ability of smart hydrogel in removing the methylene blue prepared by using two different radiation methods. The extracted pectin from the dragon fruit peel (Hylocereus polyrhizus) was used with acrylic acid (AA) to produce a polymerized hydrogel through gamma and microwave radiation. The optimum hydrogel swelling capacity was obtained by varying the dose of radiation, pectin to AA ratio and pH used. From the array of samples, the ideal hydrogel was obtained at pH 8 with a ratio of 2:3 (pectin: AA) using 10 kGy and 400 W radiated gamma and microwave respectively. The performance of both hydrogels namely as Pc/AA(G) (gamma) and Pc/AA(Mw) (microwave) were investigated using methylene blue (MB) adsorption studies. In this study, three variables were manipulated, pH and MB concentration and hydrogel mass in order to find the optimum condition for the adsorption. Results showed that 20 mg of Pc/AA(G) performed the highest MB removal which was about 45% of 20 mg/L MB at pH 8. While 30 mg of Pc/AA(Mw) able to remove up to 35% of 20 mg/L MB at the same pH condition. To describe the adsorption mechanism, both kinetic models pseudo-first-order, pseudo-second-order were employed. The results from kinetic data showed that it fitted the pseudo-first-order as compared to pseudo-second-order model equation. This study provides alternative of green, facile and affective biomaterial for dye absorbents that readily available.

Pectin microgel particles as high adsorption rate material for methylene blue: Performance, equilibrium, kinetic, mechanism and regeneration studies.

The pectin gel has been proved to be an effective material for methylene blue (MB) removal, but it presented low adsorption rate. To get over the vice, the pectin microgel particles (PMP) was prepared. No matter high or low initial MB concentration, the PMP presented high adsorption rate with equilibrium time of 20min. The adsorption process based on monolayer adsorption and adsorbance of 284.09mg/g was obtained. What's more, the adsorption process was electrostatic adsorption with mean free energy of 74.223kJ/mol. The pseudo-second-order kinetic model fitted perfectly to the experimental data. The MB uptake was controlled by film diffusion mechanism. Furthermore, the recovery efficiency of regenerated PMP were higher than 80% after three cycles. The present study showed the PMP presented acceptable adsorbance, high adsorption rate and recovery efficiency. Thus, we believe that the PMP was a promising candidate for MB cleanup.

Synchronized methylene blue removal using Fenton-like reaction induced by phosphorous oxoanion and submerged plasma irradiation process.

In this study, a combination of phosphorus (PP) oxoanions in a submerged plasma irradiation (SPI) system was used to enhance the removal efficiency of dyes from wastewater. The SPI system showed synergistic methylene blue removal efficiency, due to the plasma irradiation and Fenton-like oxidation. The ferrous ions released from the iron electrode in the SPI system under plasmonic conditions form complexes with the PP anions, which can then react with dissolved oxygen (O2) or hydrogen peroxide (H2O2) via Fenton-like reactions. The experimental results revealed that a sodium triphosphate (TPP) combined SPI system has a higher dye removal efficiency than a tetrasodium pyrophosphate (DP) or a sodium hexametaphosphate (HMP) combined SPI system under similar dissolved iron ion concentrations. To confirm the accuracy of the proposed removal mechanism via Fenton-like oxidation, it was compared to SPI systems under an oxygen environment (TPP/SPI/O2 (k = 0.0182 s-1)) and a nitrogen environment (TPP/SPI/N2 (k = 0.0062 s-1)). The results indicate that the hydroxyl radical (OH) in the TPP/SPI/O2 system is the major oxidant in methylene blue removal, because the dye degradation rates dramatically decreased with the addition of radical scavengers such as tert-butanol (k = 0.0023 s-1) and methanol (k = 0.0021 s-1). On the other hand, no change was observed in the methylene blue removal efficiency of the TPP/SPI/O2 system when it was subjected to a wide range of pHs (3-9). In addition, it was proved that this system could be used to eliminate six different commercial dyes. The results of this study indicated that the TPP/SPI/O2 system is a promising advanced oxidation approach for dye wastewater treatment.

Study of the effect of an acid treatment of a natural Moroccan bentonite on its physicochemical and adsorption properties.

In this study, a natural bentonite taken from a deposit in the Northeast of Morocco has been purified (PB) and treated with various HCl molarities (xHPB) in order to obtain an HCl/Bentonite weight ratio equal to 0.2, 0.4 and 0.6. The obtained physicochemical characterization results indicated that the PB sample is composed mainly of the montmorillonite phase. The impact of acid treatment was investigated by identifying changes in the chemical composition, cation exchange capacity, infrared absorption bands, crystalline structure, morphology of the particles and specific surface area. The adsorption behavior of methylene blue (MB) and methyl orange (MO) in aqueous solution onto PB and xHPB samples was investigated by varying the initial concentration of dyes, the contact time and the temperature. The obtained results showed that the experimental data best fit the Langmuir model and the pseudo-second-order kinetic model. X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR) studies carried out after MB and MO adsorption onto PB samples indicated that MB cations were intercalated, in the form of monomers and dimers, with a large amount of monomers, slightly tilted against the plane of the clay surface. While MO molecules adsorb, with a near perpendicular alignment, with their SO3- group and O- atoms facing the mineral surface plane.

Cross-linked beads of activated oil palm ash zeolite/chitosan composite as a bio-adsorbent for the removal of methylene blue and acid blue 29 dyes.

Cross-linked beads of activated oil palm ash zeolite/chitosan (Z-AC/C) composite were prepared through the hydrothermal treatment of NaOH activated oil palm ash followed by beading with chitosan. The effects of initial dye concentration (50-400mg/L), temperature (30°C-50°C) and pH (3-13) on batch adsorption of methylene blue (MB) and acid blue 29 (AB29) were studied. Adsorption of both dyes was better described by Pseudo-second-order kinetics and Freundlich isotherm model. The maximum adsorption capacities of Z-AC/C were 151.51, 169.49, and 199.20mg/g for MB and 212.76, 238.09, and 270.27mg/g for AB29 at 30°C, 40°C, and 50°C, respectively.

Novel synthesis of a versatile magnetic adsorbent derived from corncob for dye removal.

Corncob, an agricultural waste, was successfully converted into a novel magnetic adsorbent by a low-temperature hydrothermal method (453K), including carbonization under saline conditions and magnetization using iron (III) salt. The resultant magnetic carbonaceous adsorbent (MCA) exhibited a porous structure with a higher specific surface area and more oxygen-containing functional groups than its carbonaceous precursor (CP), which can be attributed to the catalytic effect of Fe (III). The adsorption behaviors of both MCA and CP could be described well by Langmuir isotherm and pseudo-second-order model. The adsorption capacity for Methylene blue (MB) revealed by adsorption isotherms were 163.93mg/g on MCA and 103.09mg/g on CP, respectively. Moreover, MCA was demonstrated as a versatile adsorbent for removal of both anionic and cationic dyes, and it showed good reusability in regeneration studies. This work provides an alternative approach for effective conversion of biomass waste and application of them in pollutant removal.

One-pot green synthesis of reduced graphene oxide (RGO)/Fe3O4 nanocomposites and its catalytic activity toward methylene blue dye degradation.

The reduced graphene oxide (RGO)/Fe3O4 nanocomposites were synthesized through a facile one-pot green synthesis by using solanum trilobatum extract as a reducing agent. Spherical shaped Fe3O4 nanoparticles with the diameter of 18 nm were uniformly anchored over the RGO matrix and the existence of fcc structured Fe3O4 nanoparticles over the RGO matrix was ensured from X-ray diffraction patterns. The amide functional groups exist in the solanum trilobatum extract is directly responsible for the reduction of Fe(3+) ions and GO. The thermal stability of GO was increased by the removal of hydrophilic functional groups via solanum trilobatum extract and was further promoted by the ceramic Fe3O4 nanoparticles. The ID/IG ratio of RGO/Fe3O4 was increased over GO, indicating the extended number of structural defects and disorders in the RGO/Fe3O4 composite. The catalytic efficiency of prepared nanostructures toward methylene blue (MB) dye degradation mediated through the electron transfer process of BH4(-) ions was studied in detail. The π-π stacking, hydrogen bonding and electrostatic interaction exerted between the RGO/Fe3O4 composite and methylene blue, increased the adsorption efficiency of dye molecules and the large surface area and extended number of active sites completely degraded the MB dye within 12 min.

Catalytic degradation of methylene blue using biosynthesized gold and silver nanoparticles.

The scientific community is searching for new synthesis methods for the production of metallic nanoparticles. Green synthesis has now become a vast developing area of research. Here we report for the first time to best of our knowledge, a new green method for the synthesis of silver and gold nanoparticles using the Kashayam, Guggulutiktham, an ayurvedic medicine. This method is nontoxic and environmentally benign. The reduction and the stabilization capacity of the ayurvedic Kashayam are described in this paper. The size and shape of the silver and gold nanoparticles can be tuned by varying the quantity of the Kashayam. The synthesized nanoparticles are characterized using UV-VIS spectroscopy, TEM, XRD and FTIR. The size dependent catalytic activity of the synthesized nanoparticles is established in the reduction of Methylene Blue (MB) by NaBH4.

Fabrication and properties of TiO2 nanofilms on different substrates by a novel and universal method of Ti-ion implantation and subsequent annealing.

We report a new, novel and universal method to fabricate high-quality titanium dioxide (TiO2) nanofilms on different substrates by a solid phase growth process of ion implantation and subsequent annealing in oxygen atmosphere. Ti ions were implanted into fused silica, soda lime glass, Z-cut quartz, or (0001) α-sapphire by a metal vapor vacuum arc (MEVVA) ion source implanter to fluences of 0.75, 1.5 and 3 × 10(17) ions cm(-2) with a nominal accelerating voltage of 20 kV. To understand the influence of the annealing temperature, time, and substrate on the formation and phase transformation of the TiO2 nanofilms, the Ti-ion-implanted substrates were annealed in oxygen atmosphere from 500 to 1000 °C for 1-6 h. The formation of TiO2 nanofilms resulted from the slow out-diffusion of implanted Ti ions from the substrates which were then oxidized at the surfaces. The thickness and phase of the nanofilms can be tailored by controlling the implantation and annealing parameters. Since the TiO2 nanofilms are formed under high temperature and low growth rate, they show good crystallinity and antibacterial properties, with good film adhesion and stability, suggesting that the TiO2 nanofilms formed by this method have great potential in applications such as antibacterial and self-cleaning transparent glass.

Magnetic composites based on metallic nickel and molybdenum carbide: a potential material for pollutants removal.

New magnetic composites based on metallic nickel and molybdenum carbide, Ni/Mo(2)C, have been produced via catalytic chemical vapor deposition from ethanol. Scanning electron microscopy, thermal analysis, Raman spectroscopy and X-ray diffraction studies suggest that the CVD process occurs in a single step. This process involves the reduction of NiMo oxides at different temperatures (700, 800 and 900°C) with catalytic deposition of carbon from ethanol producing molybdenum carbide on Ni surface. In the absence of molybdenum the formation of Ni/C was observed. The magnetic molybdenum carbide was successfully used as pollutants removal by adsorption of sulfur and nitrogen compounds from liquid fuels and model dyes such as methylene blue and indigo carmine. The dibenzothiofene adsorption process over Ni/Mo(2)C reached approximately 20 mg g(-1), notably higher than other materials described in the literature and also removed almost all methylene blue dye. The great advantage of these carbide composites is that they may be easily recovered magnetically and reused.

Adsorption of basic dye from wastewater using raw and activated red mud.

Red mud, an industrial by-product generated during the processing of bauxite ore, was investigated as an inexpensive and effective adsorbent for the adsorption of methylene blue from aqueous solution. Chemical and heat treatments were applied to the raw red mud. The effects of contact time, adsorbent amount, pH, temperature and initial dye concentration were investigated. The adsorption isotherm and kinetics of the raw and activated red mud were studied. Freundlich, Temkin and Dubinin-Radushkevich isotherms were obtained using concentrations of methylene blue ranging from 10 to 70 mg/L. The results indicated that the Dubinin-Radushkevich model provides the best correlation of the experimental data. The adsorption rate data were analysed according to the pseudo-first order kinetic, pseudo-second order kinetic, intraparticle diffusion kinetic and Elovich kinetic models. The pseudo-second order kinetic was the best fit kinetic model for the experimental data.

Stabilization of a magnetic nano-adsorbent by extracted pectin to remove methylene blue from aqueous solution: a comparative studying between two kinds of cross-linked pectin.

The removal of methylene blue (MB) as a cationic dye from aqueous solution by the stabilized Fe(3)O(4) nano-particles with the extracted pectin from apple waste (FN-PA) increased due to using the cross-linked forms of the bound pectin on the nano-particles surface by glutaraldehyde (FN-PAG) and adipic acid (FN-PAA) as the cross-linking agents. This increase happened in spite of binding some of the adsorbent functional groups of pectin with nano-particles. It can be due to the local concentrate of other free functional groups after connecting with nano-scale particles. Thermodynamic studies showed that the adsorption equilibrium constant and the maximum adsorption capacities increased with increasing temperature for all of the nano-bioparticles. The kinetic followed the second-order models with the highest rate constants viz. 16.23, 19.76 and 23.04 (× 10(-3)g/mg min) by FN-PAA. The adsorption force arrangement of MB by these nano-biosorbents regarding their activation energy was obtained as: FN-PAA>FN-PAG>FN-PA.

Rejected tea as a potential low-cost adsorbent for the removal of methylene blue.

The adsorption of methylene blue (MB) from aqueous solution using a low-cost adsorbent, rejected tea (RT), has been studied by batch adsorption technique. The adsorption experiments were carried out under different conditions of initial concentration (50-500 mg/L), solution pH 3-12, RT dose (0.05-1g) and temperature (30-50 degrees C). The equilibrium data were fitted to Langmuir and Freundlich isotherms and the equilibrium adsorption was best described by the Langmuir isotherm model with maximum monolayer adsorption capacities found to be 147, 154 and 156 mg/g at 30, 40 and 50 degrees C, respectively. Three kinetic models, pseudo-first-order, pseudo-second-order and intraparticle diffusion were employed to describe the adsorption mechanism. The experimental results showed that the pseudo-second-order equation is the best model that describes the adsorption behavior with the coefficient of correlation R(2)>or=0.99. The results suggested that RT has high potential to be used as effective adsorbent for MB removal.

Adsorptive removal of methylene blue by tea waste.

The potentiality of tea waste for the adsorptive removal of methylene blue, a cationic dye, from aqueous solution was studied. Batch kinetics and isotherm studies were carried out under varying experimental conditions of contact time, initial methylene blue concentration, adsorbent dosage and pH. The nature of the possible adsorbent and methylene blue interactions was examined by the FTIR technique. The pH(pzc) of the adsorbent was estimated by titration method and a value of 4.3+/-0.2 was obtained. An adsorption-desorption study was carried out resulting the mechanism of adsorption was reversible and ion-exchange. Adsorption equilibrium of tea waste reached within 5h for methylene blue concentrations of 20-50mg/L. The sorption was analyzed using pseudo-first-order and pseudo-second order kinetic models and the sorption kinetics was found to follow a pseudo-second order kinetic model. The extent of the dye removal increased with increasing initial dye concentration. The equilibrium data in aqueous solutions were well represented by the Langmuir isotherm model. The adsorption capacity of methylene blue onto tea waste was found to be as high as 85.16mg/g, which is several folds higher than the adsorption capacity of a number of recently studied in the literature potential adsorbents. Tea waste appears as a very prospective adsorbent for the removal of methylene blue from aqueous solution.

Batch adsorption of methylene blue from aqueous solution by garlic peel, an agricultural waste biomass.

The potential of garlic peel (GP), agricultural waste, to remove methylene blue (MB) from aqueous solution was evaluated in a batch process. Experiments were carried out as function of contact time, initial concentration (25-200mg/L), pH (4-12) and temperature (303, 313 and 323 K). Adsorption isotherms were modeled with the Langmuir, Freundlich, and Temkin isotherms. The data fitted well with the Freundlich isotherm. The maximum monolayer adsorption capacities were found to be 82.64, 123.45, and 142.86 mg/g at 303, 313, and 323 K, respectively. The kinetic data were analyzed using pseudo-first-order and pseudo-second-order models. The results indicated that the garlic peel could be an alternative for more costly adsorbents used for dye removal.

Preparation of activated carbons from coffee husks utilizing FeCl3 and ZnCl2 as activating agents.

Ferric chloride was used as a new activating agent, to obtain activated carbons (AC) from agro industrial waste (coffee husks). This material was compared with two samples from the same raw material: one of them activated by using the classical activating agent, zinc chloride, and the other, activated with a mixture of the two mentioned activating agents in the same mass proportion. The carbonaceous materials obtained after the activation process showed high specific surface areas (BET), with values higher than 900 m(2)g(-1). It is interesting to observe that the activation with FeCl(3) produces smaller pores compared to the activation with ZnCl(2). An important fact to emphasize in the use of FeCl(3) as activating agent is the activation temperature at 280 degrees C, which is clearly below to the temperature commonly employed for chemical or physical activation, as described in the bibliography. All the studied materials showed different behaviors in the adsorption of methylene blue dye and phenol from aqueous solutions.

Characterization of carbons from olive cake by sorption of wastewater pollutants.

Studies has been conducted to compare the sorption properties between raw carbons made from olive cake and commercial activated carbons to remove aquatic pollutant such as heavy metal (HM), phenol (Ph), dodecylbenzenesulfonic acid-sodium salt detergent (DBSNa) and methylene blue dye (MB). Effect of acidic treatments by H2SO4, HCl and HNO3 on the sorption properties of olive cake carbon (OCC) were studied by mass titration, SEM photographs, sorption isotherms. It is found that acidic treatment changes the surface properties of OCC but do not enhance its sorption capacity. Compared to commercial activated carbons the OCC derivatives generally are equally able to uptake HM and Ph from solution but MB and DBSNa are not. This different behaviour is to attribute to manufacturing and activation treatments so as surface groups of the precursor sorbent material. For the heavy metals, chromium and silver were removed effectively but to small extent cadmium. This may be because of the various charge densities of metal elements tested. The results of the multiple experiments indicate that sorption of cadmium ions can be significantly improved by the presence of complexing agents sorbed from the carbon. An empirical mathematical form is proposed to correlate experimental data and to compare the performance of the different sorbent materials.