Quartzite an efficient adsorbent for the removal of anionic and cationic dyes from aqueous solutions

Quartzite obtained from local source was investigated for the removal of anionic dye congo red (CR) and cationic dye malachite green (MG) as an adsorbent from aqueous solution in batch experiment. The adsorption process was studied as a function of dye concentration, contact time, pH and temperature. Adsorption process was described well by Langmuir and Freundlich isotherms. The adsorption capacity remained 666.7 mg/g for CR dye and 348.125 mg/g for MG dye. Data was analyzed thermodynamically, ΔH⁰ and ΔG⁰ values proved that adsorption of CR and MG is an endothermic and spontaneous process. Adsorption data fitted best in the pseudo-first order kinetic model. The adsorption data proved that quartzite exhibits the best adsorption capacity and can be utilized for the removal of anionic and cationic dyes.     

Optimization of modification condition of nano-kaoline as an adsorbent for textile dye removal

In this study, adsorption capacity of textile red dye on alkylated kaolin was investigated through batch mode. Accordingly, raw kaolin was alkylated via NaOH treatment. The work was carried out in two steps. At first step, the effect of various alkylation conditions of kaolin on its dye adsorption performance was studied using the model equation designed by 2-level factorial design. Three factors were changed in two level including NaOH solution temperature (45–75°C), mixing time (3–24 h), and NaOH solution concentration (0.1–2 M). The resultant model showed 91% of the variability in data used to fit dye adsorption capacity values. However, the analysis of variance revealed that the fitted model is high significant. Based on the predicting model, the optimal alkylation conditions with desirability factor of 0.911 were obtained at temperature of 75°C, NaOH concentration of 0.1 M and after 24 h mixing. At step two, chemical content, bonds and functional groups of the treated kaolin, which was prepared based on the optimum condition and compared with the raw kaolin via X-ray fluorescence (XRF) analysis and Fourier transform infrared analysis (FTIR). The results show slight reduction in SiO₂ content. Finally, the adsorption capacity of dye on both treated and raw kaolin was investigated.     

Use of titanium dioxide photocatalysis on the remediation of model textile wastewaters containing azo dyes

The photocatalytic degradation of two commercial textile azo dyes, namely C.I Reactive Black 5 and C.I Reactive Red 239, has been studied. TiO(2) P25 Degussa was used as catalyst and photodegradation was carried out in aqueous solution under artificial irradiation with a 125 W mercury vapor lamp. The effects of the amount of TiO(2) used, UV-light irradiation time, pH of the solution under treatment, initial concentration of the azo dye and addition of different concentrations of hydrogen peroxide were investigated. The effect of the simultaneous photodegradation of the two azo dyes was also investigated and we observed that the degradation rates achieved in mono and bi-component systems were identical. The repeatability of photocatalytic activity of the photocatalyst was also tested. After five cycles of TiO(2) reuse the rate of colour lost was still 77% of the initial rate. The degradation was followed monitoring the change of azo dye concentration by UV-Vis spectroscopy. Results show that the use of an efficient photocatalyst and the adequate selection of optimal operational parameters may easily lead to a complete decolorization of the aqueous solutions of both azo dyes.     

Raman spectrometry as a screening tool for solvent-extracted azo dyes from polyester-based textile fibres

Some types of textile fibres are considered to be the cause of allergic reactions and other adverse health effects on humans. The main compounds behind these health problems usually contain azo groups in their chemical structure, which are widely employed as azo dyes in the manufacture of textile and clothing products. In this respect, availability of simple analytical procedures for identifying azo groups in textiles is of concern, not only for toxicological studies, but also for clinical and forensic investigations. In this work, conventional Raman spectrometry was assessed as an analytical tool for identification of the azo function in the extracts of fibres obtained after applying a liquid-solvent extraction procedure to the polyester-based textile products. A medium-polarity solvent of ethanol-diethyl ether (1:1 mixture) was shown to be the most effective extraction medium. Two laser lines at 514.5 nm and 785 nm were compared, with the longer wavelength preferred as additional peaks were identified in the Raman spectrum, which had better signal-to-background and signal-to-noise ratios owing to decreased fluorescence in contrast to excitation at 514.5 nm. The method reported is a convenient procedure that can be applied in many instances when rapid screening of fibre dyes is required.     

Polyacrylic acid/polyaniline composite as efficient adsorbent for uranium extraction from nuclear industrial effluent

Journal of Radioanalytical and Nuclear Chemistry - Polyacrylic acid/polyaniline composite (a three-dimensional cross-linked hydrophilic chelating polymeric sorbent) was improved for promoted...     

Novel adsorbent based on silkworm chrysalides for removal of heavy metals from wastewaters

In this contribution, maximum capacity for adsorption of Pb(2+), Ni(2+), and Cu(2+) by silkworm chrysalides (SC) was determined. The raw silkworm chrysalides (SC(r)) and chrysalides after acidic washing (SC(w)) were used. Chitin (CT), extracted from SC, and chitosan (CS), with 85% deacetylation, were employed as reference samples. Adsorption tests showed that all the studied adsorbents exhibited excellent performance in removal of metals. The choice of a more appropriate adsorbent is related to its efficiency for removal of a specific metal. The studied materials presented different intensities for metal adsorption as follows: (i) Ni(2+)>Cu(2+)>Pb(2+) for SC(r); (ii) Pb(2+)>Cu(2+)>Ni(2+) for SC(w); (iii) Ni(2+)>Cu(2+)>Pb(2+) for CT; and (iv) Cu(2+)>Pb(2+)>Ni(2+) for CS. Metal adsorption onto SC(r) and CS was analyzed by Freundlich and Langmuir isotherm equations. Adsorption values for CS-Pb and SC(r)-Ni were provided by the Freundlich model, while the adsorption values for CS-Cu, CS-Ni, SC(r)-Pb, and SC(r)-Cu were provided by the Langmuir model. The studied adsorbents are suitable for use in treatment of wastewater. From the economic point of view, the use of SC(r) as an adsorbent of heavy metals (mainly Ni(2+)) on the large industrial scale would be more appropriate.     

Fe3O4-CuO-activated carbon composite as an efficient adsorbent for bromophenol blue dye removal from aqueous solutions

Dye wastewater from industries is posing tremendous health hazards. The lethal dyes can be eliminated using nanomaterials and scientific approach like adsorption which is facile, cheap, safe as well as ecofriendly. Fe₃O₄-CuO-AC composite was prepared by a hydrothermal method and used for the removal of dyes in wastewater. The composite material was characterized by various techniques such as XRD, SEM, EDS, TEM and FT-IR. The Fe₃O₄-CuO-AC composite was used to treat five types of dyes in water. Fe₃O₄-CuO-AC composite showed the highest adsorption capability for bromophenol blue (BPB) dye. The effects of initial concentration, pH, the amount of adsorbent and temperature were also studied. The optimum conditions were found to be 20 ppm dye concentration, pH 9, an adsorbent dose of 0.06 gL^─1 at 65 °C. A removal efficiency of 97% was obtained for BPB dye during 120 min of adsorption. Kinetic studies indicated that a pseudo-second order is the most suitable model for the adsorption process. The Fe₃O₄-CuO-AC composite showed better adsorption capacity as compare to Fe₃O₄-AC except for the Methyl green dye. The maximum adsorption capacity was found to be 88.60 mg/g for BPB. Additionally, the thermodynamic parameters (ΔS°, ΔH° and ΔG°) showed that the process was spontaneous and exothermic. All the above results revealed that the Fe₃O₄-CuO-AC compositecan be an effective adsorbent for removing dyes from wastewater.     

Effective removal of anionic dyes from aqueous solutions by novel polyethylenimine-ozone oxidized hydrochar (PEI-OzHC) adsorbent

The adsorption behavior of the anionic dyes Remazol Brilliant Blue R (RBBR) and Reactive Black 5 (RB5) from aqueous solutions by polyethylenimine ozone oxidized hydrochar (PEI-OzHC) was investigated. The adsorption capacities of both dyes increased with functionalization of PEI in the hydrochar adsorbent. The results of surface characterization (FTIR, BET, TGA, elemental analysis, and SEM) showed that PEI modification greatly enhanced the adsorbent surface chemistry with a slight improvement of adsorbent textural properties. In addition, the adsorption kinetics data showed an excellent adsorption efficiency as reflected in the high removal percentages of the anionic dyes. The Isotherm results indicated that RBBR and RB5 dye adsorption occurred via monolayer adsorption, and chemisorption was the rate-controlling step. The PEI-OzHC adsorbent possesses higher maximum Langmuir adsorption capacity towards RBBR (218.3 mg/g) than RB5 (182.7 mg/g). This increase in adsorption capacity is attributed to the higher number of functional groups in RBBR that interact with the adsorbent. This study reveals the potential use of adsorbents derived from pine wood hydrochar in municipal as well as industrial wastewater treatment. Furthermore, surface chemistry modification is proven as an effective strategy to enhance the performance of biomass-derived adsorbents.     

Amidoamine calix[4]resorcinarene-based oligomers and polymers as efficient sorbents of azo dyes from water

The sorption behaviour of three kinds of macrocyclic sorbents – amidoamine tetradodecyloxyphenylencalix[4]resorcinarene 1 and tetramethyloxyphenylencalix[4]-resorcinarene 2; composition of calix[4]resorcinarene 1+2, and novel P.1 and P.2 polymers with amidoamine calix[4]resorcinarene units towards three water-soluble azo dyes – methyl orange (MO), acid orange (AO5) and Congo red (CR) was studied. All sorbents form supramolecular complexes with the aforesaid dyes. The best sorbent for MO was shown to be polymer P.1, for the AO5 – composition 1+2 and for the CR – macrocycle 2, with high sorption capacities (373, 497 and 625 mg/g, respectively). The main factor in the binding of dyes by all studied sorbents proved to be surface electrostatic interactions. In addition to the Coulomb interactions, the most important factor for the polymers appeared to be the ‘net’ structure of the polymer with a high concentration of binding sites, providing electrostatic, hydrogen, dipole–dipole and hydrophobic interaction. Hydrophobic substituents in the sorbents exert a significant influence on the dye sorption. The increase of the sorbents' hydrophobicity leads to a lower sorption capacity for MO and CR and a higher sorption capacity for AO5. It was shown that sorption efficiency of the sorbent depends on the ‘dye–sorbent’ structure conformity.     

The removal of textile dyes by diatomite earth

The adsorption of some textile dyes by diatomite was investigated using Sif Blau BRF (SB), Everzol Brill Red 3BS (EBR), and Int Yellow 5GF (IY). Adsorption of these textile dyes onto diatomite earth samples was studied by batch adsorption techniques at 30 degrees C. The adsorption behavior of textile dyes on diatomite samples was investigated using a UV-vis spectrophotometric technique. The effect of particle size of diatomite, diatomite concentration, the effect of initial dye concentrations, and shaking time on adsorption was investigated. Adsorption coverage over the surface of diatomite was studied using two well-known isotherm models: Langmuir's and Freundlich's. These results suggest that the dye uptake process mediated by diatomite has a potential for large-scale treatment of textile mill discharges. According to the equilibrium studies, the selectivity sequence can be given as IY > SB > EBR. Values of the removal efficiency of the dyes ranged from 28.60 to 99.23%. These results show that natural diatomite holds great potential to remove textile dyes from wastewater.     

Removal of dyes from colored textile wastewater by orange peel adsorbent: equilibrium and kinetic studies

The use of low-cost and ecofriendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. Orange peel was collected from the fields of orange trees in the north of Iran and converted into a low-cost adsorbent. This paper deals with the removal of textile dyes from aqueous solutions by orange peel. Direct Red 23 (DR23) and Direct Red 80 (DR80) were used as model compounds. The adsorption capacity Q0 was 10.72 and 21.05 mg/g at initial pH 2. The effects of initial dye concentration (50, 75, 100, 125 mg/l), pH, mixing rate, contact time, and quantity of orange peel have been studied at 25 degrees C. The Langmuir and Freundlich models were used for this study. It was found that the experimental results show that the Langmuir equation fit better than the Freundlich equation. The results indicate that acidic pH supported the adsorption of both dyes on the adsorbent. Orange peel with concentrations of 8 and 4 g/l has shown adsorption efficiencies of about 92 and 91% for DR23 and DR80, respectively. Furthermore, adsorption kinetics of both dyes was studied and the rates of sorption were found to conform to pseudo-second-order kinetics with a good correlation (R > or = 0.998). Maximum desorption of 97.7% for DR23 and 93% for DR80 were achieved in aqueous solution at pH 2. Finally, the effect of adsorbent surface was analyzed by scanning electron microscope (SEM). SEM images showed reasonable agreement with adsorption measurements.     

Fabrication of SiO2/CuFe2O4/polyaniline composite: A highly efficient adsorbent for heavy metals removal from aquatic environment

A novel multifunctional of SiO₂/CuFe₂O₄/polyaniline composite was synthesized through the interaction between silica (SiO₂), copper iron oxide (CuFe₂O₄), and polyaniline (PANI) as starting materials. SiO₂/CuFe₂O₄/polyaniline composite was characterized for morphology, crystallinity, textural properties, and utilised for the removal of Fe(II), Mn(II), and Cu(II) from synthetic wastewater solutions. The roles of solution pH (2.0–6.0), interaction time (15–420 min), initial ion concentration (50–700 mg/L), and solution temperature (30–50 °C) in the adsorption process were investigated. The adsorption capacities of SiO₂/CuFe₂O₄/PANI for the tested metal ions were high compared to SiO₂, CuFe₂O_4, and polyaniline. Equilibrium studies indicated that Fe(II) and Mn(II) adsorption were compliant with the Langmuir model, while the Freundlich equation described the removal of Cu(II) ions. The maximum Langmuir capacities were up to 285.71, 416.67, and 454.55 mg/g for Cu(II), Fe(II), and Mn(II), respectively. The pseudo-first-order kinetic model fitted well the metal ions removal data. The rate-controlling step reflected the involvement of surface and inner pore diffusion (intraparticle) processes. Electrostatic attractions and chelation were mainly responsible for the binding of metals ions onto SiO₂/CuFe₂O₄/PANI. The selectivity of the studied ions was governed mainly by the hydrated ionic radii and the composite adsorption active sites. SiO₂/CuFe₂O₄/PANI can be easily reused with a slight decrease (around 2–3%) in metal removal efficiency after four successive regeneration cycles.     

Electrically enhanced liquid‐phase microextraction of three textile azo dyes from wastewater and plant samples

An electromembrane extraction procedure coupled with HPLC and visible detection was applied for the extraction of three textile azo dyes as organic salts. The extraction parameters such as extraction time, applied voltage, pH range, and concentration of salt added were optimized. A driving force of 60 V was applied to extract the analytes through 2‐nitrophenyl octyl ether, used as the supported liquid membrane, into a neutral aqueous solution. This method required 20 min extraction time from a neutral sample solution. The proposed microextraction technique provided good linearity with correlation coefficients from 0.996 to 0.998 over a concentration range of 1.0–1000.0 ng/mL. The LODs of dyes were 0.30–0.75 ng/mL, while the reproducibility ranged from 6.7 to 12.9% (n = 6). Also, enrichment factors of 96–162 that corresponded to the recoveries ranging from 48 to 81% were achieved. Finally, the application of this new method was demonstrated on wastewater samples and some plants grown in contaminated environments. Excellent selectivity was obtained as no interfering peaks were detected.     

Aminophenyl-X-azolopyridines as precursors of heterocyclic azo dyes

Aminophenyl-X-azolopyridines (X = O, S, NH) are interesting intermediates for the synthesis of disperse azo dyes and, provided the pyridine nitrogen is quaternized, of their cationic counterparts. A set of novel amines and nitro derivatives is described, and their physical properties and spectral parameters are discussed in comparison with those of analogous compounds. Some dyes in the oxazole series function as probes of the reactivity of the pentatomic ring.     

Evaluation of an activated carbon from olive stones used as an adsorbent for heavy metal removal from aqueous phases

The performance of a microporous activated carbon prepared chemically from olive stones for removing Cu(II), Cd(II) and Pb(II) from single and binary aqueous solutions was investigated via the batch technique. The activated carbon sample was characterized using N₂ adsorption–desorption isotherms, SEM, XRD, FTIR, and Boehm titration. The effect of initial pH and contact time were studied. Adsorption kinetic rates were found to be fast and kinetic experimental data fitted very well the pseudo-second-order equation. The adsorption isotherms fit the Redlich–Peterson model very well and maximum adsorption amounts of single metal ions solutions follow the trend Pb(II) > Cd(II) > Cu(II). The adsorption behavior of binary solution systems shows a relatively high affinity to Cu(II) at the activated carbon surface of the mixture with Cd(II) or Pb(II). An antagonistic competitive adsorption phenomenon was observed. Desorption experiments indicated that about 59.5% of Cu(II) and 23% of Cd(II) were desorbed using a diluted sulfuric acid solution.     

Porous glass as an efficient adsorbent for volatile atmospheric polychlorinated biphenyl congeners

Porous glass is a more efficient adsorbent than Amberlite XAD-2 resin for volatile polychlorobiphenyls (PCB) in the atmospheric vapour phase. The adsorption efficiencies for individual PCB congeners are compared by analysis of the extracts by capillary gas chromatography (electron-capture detection); individual congeners are used as reference compounds. Efficiencies for some di-, tri- and tetra-chlor congeners are between 1.7 and 7 times higher the porous glass than for XAD-2 resin; values for penta-, hexa- and hepta-chloro congeners are very similar. The calculated “total” PCB (as the sum of individual congeners) was about four times higher for porous glass, because of the contribution from congeners with low chlorine numbers. Commercial mixtures may not reflect the real composition of PCB mixtures in the atmosphere.     

Review of MXenes as a component in smart textiles and an adsorbent for textile wastewater remediation

Two-dimensional(2D) MXenes have emerged as an archetypical layered material combining the properties of an organic-inorganic hybrid offering materials sustainability for a range of applications. Their surface functional groups and the associated chemical properties’ tailorability through functionalizing MXenes with other materials as well as hydrophilicity and high conductivity enable them to be the best successor for various applications in textile industries, especially in the advancement of s...     

A novel color removal adsorbent from heterocoagulation of cationic and anionic clays

We report the preparation and characterization of a novel nanocomposite adsorbent for anionic dye removal. The nanocomposite adsorbent was prepared by heterocoagulation of delaminated bentonite and layered double hydroxide (LDH) colloids. The effects of preparation conditions, LDH loading, particle size, and calcination temperature of the modified material on the physicochemical properties of this composite adsorbent have been investigated. The optimal conditions for best Reactive Yellow 2 (RY2) dye removal efficiency are a weight ratio of LDH to bentonite of 1:1, LDH particle size 100 nm, and calcination temperature 673 K. The adsorption equilibrium data can be fitted well by the widely accepted adsorption isotherm models.     

Nano-iron oxide-encapsulated chitosan microspheres as novel adsorbent for removal of Ni (II) ions from aqueous solution

The present study investigates the utility of composite beads of nano-particles of iron oxide and chitosan for removing Ni (II) ions from aqueous solution by batch and column adsorption techniques. In the batch mode experiment, the influence of pH, concentration, adsorbent dose, temperature, column mode, bed height, flow rate and initial concentration were studied on the adsorption profiles of nickel ions. The maximum uptake of Ni (II) ions was obtained at pH 4.0 in 30 min at room temperature.