Synthesis,characterization and adsorption of cationic dyes by CS/P(AMPS-<Emphasis Type="Italic">co</Emphasis>-AM) hydrogel initiated by glow-discharge-electrolysis plasma

In this work, a novel chitosan/P(2-acrylamido-2-methyl-1-propanesulfonic acid-co-acrylic amide) (CS/P(AMPS-co-AM)) hydrogel was successfully prepared by a simple one-step method using glow-discharge-electrolysis plasma (GDEP) initiated copolymerization, in which N,N′-methylenebisacrylamide was used as a cross-linking agent. A copolymerization mechanism of AMPS and AM onto CS initiated by GDEP was proposed. The structure, thermal stability and morphology of CS/P(AMPS-co-AM) hydrogel were characterized by Fourier transform infrared (FTIR), X-ray diffraction (XRD), TG/DTG, and scanning electron microscope (SEM). This hydrogel was employed as an absorbent for the removal of methylene blue (MB) and malachite green (MG) from aqueous solutions. The effects of pH, contact time and equilibrium concentration on the dye adsorption were investigated batchwise. FTIR and XRD indicated that AM and AMPS were grafted onto the CS backbone successfully, forming copolymer. TG/DTG suggested that grafted AMPS and AM onto CS could change the thermal stability of the CS. SEM showed a unique three-dimensional porous structure for the CS/P(AMPS-co-AM) hydrogel. The optimum pH for the removal of cationic dyes was 5.8, and time of adsorption equilibrium was achieved in 90 min. The CS/P(AMPS-co-AM) hydrogel exhibited a very high adsorption potential, and its adsorption capacities calculated based on the Langmuir isotherm for MB and MG were 1,538.5 and 917.4 mg g^?1, respectively. The dye adsorption data fitted well to the pseudo-second-order model and Langmuir model at 25 °C with pH 5.8.     

Adsorption of selected dyes on Ti3C2Tx MXene and Al-based metal-organic framework

MXene and metal organic framework (MOF) were used as the main adsorbents to remove synthetic dyes from model wastewater. Methylene blue (MB) and acid blue 80 (AB) were used as the model cationic and anionic synthetic dyes, respectively. To investigate the physicochemical properties of the adsorbents used, we carried out several characterizations using microscopy, powder X-ray diffraction, a porosimetry, and a zeta potential analyzer. The surface area of MXene and MOF was 9 and 630 m² g⁻¹, respectively, and their respective isoelectric points were approximately pH 3 and 9. Thus, MXene and MOF exhibited high capacity for MB (~140 mg g⁻¹) and AB (~200 mg g⁻¹) adsorption, respectively due to their electrostatic attractions when the concentrations of the adsorbents and adsorbates were 25 and 10 mg L⁻¹. Furthermore, the MOF was able to capture the MB due mainly to hydrophobic interactions. In terms of the advantages of each adsorbent according to our experimental results, MXene exhibited fast kinetics and high selectivity. Meanwhile, the MOF had a high adsorption capacity for both MB and AB. The adsorption mechanisms of both adsorbents for the removal of MB and AB were clearly explained by the results of our analyses of solution pH, ionic strength, and the presence of divalent cation, anion, or humic acids, as well as other characterizations (i.e., Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy). According to our results, MOF and MXene can be used as economical treatments for wastewater containing organic pollutants regardless of charge (e.g., MB and AB), and positively charged one (e.g., MB), respectively.     

ZnO/Cassava Starch-Based Hydrogel Composite for Effective Treatment of Dye-Contaminated Wastewater

Industrial expansion has increased the discharge of contaminated wastewater. Wastewater can be treated by adsorption with petroleum-based hydrogels but the materials are not biodegradable and therefore cause secondary toxic waste. In this work, hydrogel composites are prepared based on non-biodegradable polyacrylamide and biodegradable materials of cassava starch (CS) and poly(vinyl alcohol). The effect of CS content on the porous structure is studied. The highest water absorption capacity of 74 g g⁻¹ is obtained from a hydrogel 30 wt% of CS. Within 4 h, the hydrogel effectively adsorbs the cationic dyes methylene blue (MB) and crystal violet, and the anionic dyes congo red and reactive orange. The maximum adsorption capacity toward MB is 993 mg g⁻¹. Experimental data indicate a monolayer adsorption via chemisorption. Silica-coated ZnO photocatalyst particles are synthesized via a sol–gel method and coated on the outer surface of the hydrogel. Under sunlight, the hydrogel composite degrades almost 90% of adsorbed dye. The hydrogel composite is capable of effective photodegradation for at least three cycles under artificial UV irradiation and four cycles under sunlight, but adsorption capacity remains higher than 80% at the eighth cycle. The hydrogel composite also shows antibacterial activities, indicating an additional beneficial property for industrial wastewater treatment.     

Synthesis and swelling behavior of metal-chelating superabsorbent hydrogels based on sodium alginate-<Emphasis Type="Italic">g</Emphasis>-poly(AMPS-<Emphasis Type="Italic">co</Emphasis>-AA-<Emphasis Type="Italic">co</Emphasis>-AM) obtained under microwave irradiation

A metal-chelating superabsorbent hydrogel based on poly(2-acrylamido-2-methylpropanesulfonic acid-co-acrylic acid-co-acrylamide) grafted onto sodium alginate backbone, NaAlg-g-poly(AMPS-co-AA-co-AM) is prepared under microwave irradiation. The Taguchi method is used for the optimization of synthetic parameters of the hydrogel based on water absorbency. The Taguchi L₉ (3⁴) orthogonal array is chosen for experimental design. Mass concentrations of crosslinker MBA \(C_{\text{MBA}}\) initiator KPS \(C_{\text{KPS}}\), sodium alginate \(C_{\text{NaAlg}}\) and mass ratio of monomers \(C_{\text{AM/AA/AMPS}}\) are chosen as four factors. The analysis of variance of the test results indicates the following optimal conditions: 0.8 g L^?1 of MBA, 0.9 g L^?1 of KPS, 8 g L^?1 of NaAlg and \(R_{\text{AM/AA/AMPS}}\) equals to 1:1.1:1.1. The maximum water absorbency of the optimized final hydrogel is found to be 822 g g^?1. The relative thermal stability of the optimized hydrogel in comparison with sodium alginate is demonstrated via thermogravimetric analysis. The prepared hydrogel is characterized by FTIR spectroscopy and scanning electron microscopy. The influence of the environmental parameters on water absorbency such as the pH and the ionic force is also investigated. The optimized hydrogel is used as adsorbent for hazardous heavy metal ions Pb(II), Cd(II), Ni(II) and Cu(II) and their competitive adsorption is also discussed. Isotherm of adsorption and effect of pH, adsorption dosage and recyclability are investigated. The results show that the maximum adsorption capacities of lead and cadmium ions on the hydrogel are 628.93 and 456.62 mg g^?1, respectively. The adsorption is well described by Langmuir isotherm model. The hydrogel is also utilized for the loading of potassium nitrate as an active agrochemical agent and the release of this active agent has also been investigated.     

Improving properties of superabsorbent composite induced by using alkaline protease hydrolyzed‐sericin (APh‐sericin)

A series of superabsorbent polymer composites based on sericin hydrolyzed with alkaline protease (AP) were prepared by grafting with acrylic acid (AA) and acrylamide (AM). The properties of the superabsorbent polymers (SAP) by using hydrolyzed sericin with different amount of alkaline protease (nAPh‐sericin) were compared. It was found that the polymer prepared from 5APh‐sericin (the mass ratio of AP to sericin was 5.0 mg g⁻¹) showed the highest graft percentage and water absorbency, this phenomenon may be attributed to the change of molecular weight of resulting sericin molecules. The molecular structure of the grafted polymers was proved by thermal gravimetric analysis (TGA) and Fourier transform infrared spectroscopy (FTIR) measurements. Comparing with PAA‐AM (poly AA‐co‐AM) and 0APh‐sericin/PAA‐AM polymer, 5APh‐sericin/PAA‐AM polymer had the most excellent water retention capacity and enzyme degradability. The morphological features of the polymers with different drying methods were evidenced by SEM images. The water absorbencies of 5APh‐sericin/PAA‐AM polymer prepared with freeze‐drying were 896 g g⁻¹ in deionized water, 424 g g⁻¹ in tap water, and 83 g g⁻¹ in 0.9 wt% aqueous NaCl solution. POLYM. COMPOS., 35:509–515, 2014. © 2013 Society of Plastics Engineers     

Investigation on preparation of carboxymethyl chitosan modified sodium ferric silicate and its adsorption properties

The layered material of sodium ferric silicate (SFS) has good adsorption properties for cationic dyes, but its stacking properties limit its application. The organic–inorganic composite assembled by macromolecular polymer and inorganic material can improve this situation. Carboxymethyl chitosan (CC) was loaded onto SFS, and the compound was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscope (TEM), Brunauer–Emmett–Teller (BET), zero energy thermonuclear assembly (Zeta), and Fourier transform infrared spectroscopy (FT-IR). The results showed that CC was successfully supported in the layered structure of SFS, and the adsorption capacity of the composite for methylene blue (MB) was 729.67 mg g⁻¹. The adsorption process was described by pseudo second-order kinetics, Langmuir isothermal equation, and intraparticle diffusion. The adsorption process was endothermic and spontaneous, and the monomolecular adsorption was dominant.     

Preparation and adsorption mechanism of polyvinyl alcohol/graphene oxide-sodium alginate nanocomposite hydrogel with high Pb(II) adsorption capacity

A series of polyvinyl alcohol (PVA)/graphene oxide (GO)-sodium alginate (SA) nanocomposite hydrogel beads were prepared through in situ crosslinking for Pb²⁺ removal. It was found that PVA and SA molecules were intercalated into GO layers through hydrogen bonding interactions, leading to the destruction of orderly structure of GO, while GO uniformly distributed in PVA matrix. With increasing PVA solution concentration, the hydrogel beads became more regular, a large number of polygonal pores with thin walls and open pores formed, the average pore size decreased, and the dense network structure formed. Meanwhile, the permeability of the composite hydrogel decreased, leading to the decline of Pb²⁺ adsorption capacity of the composite hydrogel. With increasing GO content, the ballability of the hydrogel beads was weakened, the pore size increased, and relatively loose network structure formed, resulting in an increase in permeability and Pb²⁺ adsorption capacity of the hydrogel, reaching up to 279.43 mg g⁻¹. Moreover, the composite hydrogel presented relatively good reusability for Pb²⁺ removal. The adsorption mechanism was explored and showed that the adsorption system of the composite hydrogel belonged to the second-order kinetic model and fitted Langmuir adsorption isotherm model for Pb²⁺ removal, which might be mono-layer chemical adsorption. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47318.     

Affinity microspheres and their application to lysozyme adsorption: Cibacron Blue F3GA and Cu(II) with poly(HEMA-EGDMA)

Lysozyme adsorption onto Cibacron Blue F3GA attached and Cu(II) incorporated poly(2-hydroxyethyl methacrylate–ethylene glycol dimethacrylate) [poly(HEMA-EGDMA)] microspheres was investigated. The microspheres were prepared by suspension polymerization. Various amounts of Cibacron Blue F3GA were attached covalently onto the microspheres by changing the initial concentration of dye in the reaction medium. The microspheres with a swelling ratio of 65%, and carrying different amounts of dye (between 1.4 and 22.5 µmol/g⁻¹) were used in the lysozyme adsorption studies. Lysozyme adsorption on these microspheres from aqueous solutions containing different amounts of lysozyme at different pH values was investigated in batch reactors. The lysozyme adsorption capacity of the dye–metal chelated microspheres (238.2 mg g⁻¹) was greater than that of the dye-attached microspheres (175.1 mg g⁻¹). The maximum lyzozyme adsorption capacities (q_m) and the dissociation constant (k_d) values were found to be 204.9 mg g⁻¹ and 0.0715 mg ml⁻¹ with dye-attached and 270.7 mg g⁻¹ and 0.0583 mg ml⁻¹ with dye–metal chelated microspheres, respectively. More than 90% of the adsorbed lysozyme were desorbed in 60 min in the desorption medium containing 0.5 M KSCN at pH 8.0 or 25 mM EDTA at pH 4.9. © 1999 Society of Chemical Industry     

Radiation-initiated chitosan-based double network hydrogel: Synthesis,characterization, and adsorption of methylene blue

A novel chitosan (CTS)-based double network Poly(2-acrylaMido-2-Methyl-1-propanesulfonic acid)/Polyacrylamide/CTS hydrogel was synthesized by irradiation initiated. Laponite RD (RD) was used as both dopant and the cross-linking agent. Then the fabricated hydrogel was applied as an efficient adsorbent to remove the methylene blue (MB) in an aqueous solution. This hydrogel has both high strength and good adsorption properties for MB. The results from Brunauer–Emmett–Teller method confirmed that the hydrogel has a large specific surface area (96 m²/g) and developed pore structure, which is available for the contact between the adsorbent and dye molecules. In the adsorption process, the RD provides plenty of negative charges as adsorption sites for MB molecules. The influence of pH, temperature, and adsorbent dose on the adsorption performance was investigated in detail. The experimental data fit well with the pseudo-second-order kinetic model and Langmuir isotherm. Besides, the mechanical strength of the hydrogel was also investigated in this work.     

A high-performance biochar produced from bamboo pyrolysis with in-situ nitrogen doping and activation for adsorption of phenol and methylene blue

Nitrogen doping is a promising method for the preparation of functional carbon materials. In this study, a nitrogen-doped porous coral biochar was prepared by using bamboo as raw material, urea as nitrogen source, and KHCO₃ as green activator through in-situ pyrolysis. The structure of the obtained biochar was characterized by various techniques including nitrogen adsorption and desorption, Raman spectroscopy, X-ray photoelectron spectrometer, and etc. The adsorption properties of nitrogen-doped biochar were evaluated with phenol and methylene blue probes. The results showed that the nitrogen source ratio had a significant effect on the evolution of pore structure of biochar. Low urea addition ratio was beneficial to the development of pore structures. The optimum specific surface area of nitrogen-doped biochar could be up to 1693 m²·g⁻¹. Nitrogen doping can effectively improve the adsorption capacity of biochar to phenol and methylene blue. Biochar prepared at 973.15 K with low urea addition ratio exhibited the highest adsorption capacity for phenol and methylene blue, and the equilibrium adsorption capacity was 169.0 mg·g⁻¹ and 499.3 mg·g⁻¹, respectively. By comparing the adsorption capacity of various adsorbents in related fields, it is proved that the nitrogen-doped biochar prepared in this study has a good adsorption effect.     

Adsorption studies of methylene blue onto ZnCl2-activated carbon produced from buriti shells (Mauritia flexuosa L.)

The present study reports the preparation of an activated carbon produced from buriti shells (AC_b) using ZnCl₂ as activating agent and its ability to remove methylene blue dye (MB) from aqueous solutions. The obtained AC_b was characterized by N₂ adsorption–desorption isotherms, SEM and FT-IR. The results show that AC_b presents microporous features with BET surface area (S_BET) of 843 m² g⁻¹ and functional groups common in carbonaceous materials. Adsorption studies were carried out and experimental data were fitted to three isotherm models (Langmuir, Freundlich, and Redlich–Peterson) and four kinetic models (pseudo-first order, pseudo-second order, Elovich, and intraparticle diffusion). The isotherm model which best fitted to experimental data was Redlich–Peterson. However, the g parameter of this model indicated that the adsorption of MB onto AC_b occurs according to the mechanism proposed by Langmuir, which showed maximum monolayer adsorption capacity of 274.62 mg g⁻¹. Kinetic studies demonstrated that the Elovich model is suitable to describe the experimental data. Moreover, it was found that the intraparticle diffusion is the limiting step of adsorption process.     

Transformation of Mytella falcata residual shell into CaAl/LDH adsorbent: Removal of methyl orange and methylene blue dyes

This study analyzed the viability of using malacoculture residue (Mytella falcata) to produce layered double hydroxides (LDHs) and for its subsequent use as an adsorbent. The CaAl/LDH-RE material was produced with calcium oxide from the residue and the CaAl/LDH-AP was produced with a commercial reagent. Both were used to remove methyl orange (MO) and methylene blue (MB) dyes. The CaAl/LDH-RE presented a surface area of 28.54 m² g⁻¹, being 65.62% larger than the CaAl/LDH-AP material (17.23 m² g⁻¹). The adsorbents showed mesopores distributed on a surface formed by plates in the form of hexagonal sheets arranged in an overlapping manner. The dosage of 0.05 g L⁻¹ obtained the removal of 95% and 97% for MO, while for MB it was 94% and 93% using the adsorbents LDH/CaAl-AP and LDH/CaAl-RE, respectively. The system reached equilibrium at 90 min for MO and 120 min for MB. The pseudo-second order model well represented the kinetic data reaching 11.36 mg g⁻¹ (CaAl/LDH-RE) and 8.42 mg g⁻¹ (CaAl/LDH-AP) for MO, and 4.47 mg g⁻¹ (CaAl/LDH-RE) and 4.14 mg g⁻¹ (CaAl/LDH-AP) for MB. The Freundlich model better represented the isothermal data, where the temperature exerted little influence. Adsorbents showed similar removal percentages in real and synthetic matrices. The LDH/CaAl-RE can be applied in up to 3 cycles, maintaining its adsorption capacity. These results corroborate the use of MFW to produce CaAl/LDH-RE, which can be used for the efficient removal of organic pollutants in an aqueous solution.     

Hydrogels with diffusion-facilitated porous network for improved adsorption performance

Porous alginate-based hydrogel beads (porous ABH) have been prepared through a facile and sustainable template-assisted method using nano-calcium carbonate and nano-CaCO₃ as pore-directing agent for the efficient capture of methylene blue (MB). The materials were characterized by various techniques. The sorption capacities of ABH towards MB were compared with pure sodium alginate (ABH-1:0) in batch and fixed-bed column adsorption studies. The obtained adsorbent (ABH-1:3) has a higher BET surface area and a smaller average pore diameter. The maximum adsorption capacity of ABH-1:3 obtained from Langmuir model was as high as 1,426.0mg g^-1. The kinetics strictly followed pseudo-second order rate equation and the adsorption reaction was effectively facilitated, approximately 50minutes to achieve adsorption equilibrium, which was significantly shorter than that of ABH-1:0. The thermodynamic parameters revealed that the adsorption was spontaneous and exothermic. Thomas model fitted well with the breakthrough curves and could describe the dynamic behavior of the column. More significantly, the uptake capacity of ABH-1:3 was still higher than 75% of the maximum adsorption capacity even after ten cycles, indicating that this novel adsorbent can be a promising adsorptive material for removal of MB from aqueous solution under batch and continuous systems.     

Chitosan/polyaniline hybrid for the removal of cationic and anionic dyes from aqueous solutions

Nanostructured chitosan/polyaniline (CH/PANI) hybrid was synthesized via in situ polymerization of aniline in the presence of chitosan. The CH/PANI hybrid was characterized by FTIR spectroscopy, X-ray diffraction, thermogravimetric analysis, and scanning electron microscopy. The CH/PANI hybrid had a nanofibrous structure with an average diameter of 70 nm. This hybrid was employed as an ecofriendly and efficient adsorbent with high adsorption capacity for the removal of Acid Green 25 (AG) and methylene blue (MB) from aqueous solutions. AG and MB were used as anionic and cationic model dyes, respectively. The CH/PANI adsorbent showed high dependence on the pH of the medium with an excellent adsorption performance and regeneration manner. The kinetics and adsorption isotherms were studied. The CH/PANI hybrid follows the pseudo second-order adsorption kinetics and Temkin isotherm model for the adsorption of both AG and MB dyes. This assumes that the enthalpy of dyes molecules decreases with the adsorption on heterogeneous surface with various kinds of adsorption sites and as well as the ability to form multilayers of the dye. Also, intraparticle diffusion was found to play an important role in the adsorption mechanism. The maximum adsorption capacity was found to be 240.4 mg g⁻¹ of AG at pH 4 and 81.3 mg g⁻¹ of MB at pH 11. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47056.     

Characterization of stabilized porous magnetite core–shell nanogel composites based on crosslinked acrylamide/sodium acrylate copolymers

Stabilized and dispersed superparamagnetic porous nanogels based on sodium acrylate (AA‐Na) and acrylamide (AM) in a surfactant‐free aqueous system were synthesized via solution polymerization at room temperature. The formation of magnetite nanoparticles was confirmed and their properties characterized using Fourier transform infrared spectroscopy. Extensive characterization of the magnetic polymer particles using transmission electron microscopy (TEM), dynamic light scattering and zeta potential measurements revealed that Fe₃O₄ nanoparticles were incorporated into the shells of poly(AM/AA‐Na). The average particle size was 5–8 nm as determined from TEM. AM/AA‐Na nanoparticles with a diameter of about 11 nm were effectively assembled onto the negatively charged surface of the as‐synthesized Fe₃O₄ nanoparticles via electrostatic interaction. Crosslinked magnetite nanocomposites were prepared by in situ development of surface‐modified magnetite nanoparticles in an AM/AA‐Na hydrogel. Scanning electron microscopy was used to study the surface morphology of the prepared composites. The morphology, phase composition and crystallinity of the prepared nanocomposites were characterized. Atomic force microscopy and argon adsorption–desorption measurements of Fe₃O₄.AM/AA indicated that the architecture of the polymer network can be a hollow porous sphere or a solid phase, depending on the AA‐Na content. © 2013 Society of Chemical Industry     

High-viscoelastic graft modified chitosan hydrophobic association polymer for enhanced oil recovery

The conventional partially hydrolyzed polyacrylamide (HPAM) is greatly restricted by its single linear molecular structure in oil reservoirs with severe reservoir conditions such as high temperature and high salt. In this article, the chitosan (CS) grafted imidazoline monomer copolymer (CS-g-AM/AA/NIDA) was prepared from N-maleyl CS (N-MCS), acrylamide (AM), acrylic acid (AA), 1-(2-N-acryloylaminoethyl)-2-oleoyl imidazoline (NIDA) by free radical copolymerization. The structure was determined by means of Fourier transform infrared spectroscopy, ¹H nuclear magnetic resonance spectroscopy, scanning electron microscope, thermal gravimetric analysis, and so forth, which confirmed the successful preparation of the copolymer with good thermal stability. Under the same conditions, compared with HPAM and copolymer CS-g-AM/AA, CS-g-AM/AA/NIDA greatly increased the viscosity of the aqueous solution and exhibited excellent shear stability (viscosity retention rate 15.62, 4.91, and 11.54% at 510 s⁻¹), temperature resistance (the viscosity retention rate reached 50.89, 24.50, and 36.59% at 120°C) and salt resistance (14,000 mg/L NaCl: viscosity retention rate up to 17.27, 8.26, and 14.60%). In addition, core flooding experiments showed that oil recovery could be enhanced by up to 8.08% by CS-g-AM/AA/NIDA. As a natural polymer material, CS has hardly been reported for polymer flooding, and it is expected to replace general polymers in tertiary oil recovery.     

Adsorption removal of Brilliant green and Safranin-O contaminants from water using a hydrogel based on carboxymethyl cellulose and sodium alginate crosslinked by epichlorohydrin

The current study investigates the adsorption properties of a chemically crosslinked hydrogel based on sodium alginate (NaALG) and carboxymethyl cellulose (CMC). The structural characteristics of the investigated hydrogel are described using information from Fourier Transform–infrared spectra, X-ray diffraction patterns and field emission scanning electron microscopy pictures. The NaALG/epichlorohydrin (ECH)/CMC hydrogel was synthesised under optimised conditions with respect to the swelling percentage. Various reaction parameters were varied to obtain the maximum swelling percentage. The synthesised hydrogel was taken as an adsorbent in the decolorisation of Brilliant green (BG) and Safranin-O (SO) dyes from water. According to the kinetic investigations, the decolorisation equilibrium of SO by NaALG/ECH/CMC was discovered in 4 hours (98.98%), while the removal of BG by NaALG/ECH/CMC took 6 hours (97.7%). Chemical processes were used to describe the decolorisation mechanisms, which significantly supported the pseudo-first-order model. NaALG/ECH/CMC hydrogel absorption was indicated to take place in monolayer adsorption form (Langmuir isotherm). The highest adsorption capacity for BG was discovered to be 864.8 mg g⁻¹ and for SO it was 193.1 mg g⁻¹, by synthesised hydrogel, where “mg” refers to the commercial colourant and not to the pure dye. Therefore, the synthesised hydrogel can be considered as a smart device for the adsorption of dye in water purification tasks.     

Bamboo charcoal modified with Cu2+ and 3-aminopropyl trimethoxy silane for the adsorption of acid fuchsin dye: Optimization by response surface methodology and the adsorption mechanism

The bamboo charcoal modified with Cu²⁺ and 3-aminopropyl trimethoxy silane (BC-Cu/Si-NH₂) was synthesized and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy dispersive spectroscopy, and surface acid–base potentiometric titration. The adsorption for acid fuchsin (AF) dyes onto BC-Cu/Si-NH₂ was investigated. Moreover, response surface methodology was performed to optimize the process parameters including pH, initial dye concentration, adsorbent dosage, and temperature. The results presented that the adsorption process was mainly influenced by initial AF concentration and adsorbent dosage. Isotherm studies revealed that the adsorption data fitted well with the Sips model and Dubinin–Radushkevich (D–R) model, which indicated the monolayer, homogeneous, and physical nature of the adsorption process. The maximum adsorption capacity calculated from D–R model could approach approximately to 14.91 mg g⁻¹ at 40 °C, and the maximum adsorption capacity of Sips reached to 10.77 mg g⁻¹ at 40 °C. The kinetic experimental data matched well with Spahn and Schlunder model as well as pseudo-second-order model. In addition, intraparticle diffusion was not the only rate-controlling step of adsorption process. Thermodynamic parameters revealed the feasibility, spontaneity, and endothermic nature of adsorption. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47728.     

Investigation of equilibrium and kinetic parameters of methylene blue adsorption onto MCM-41

Mesoporous MCM-41 was synthesized at room temperature using tetraethoxysilane (TEOS) with cetyltrimethylammonium bromide (CTAB) and employed as an effective adsorbent for the adsorption of methylene blue dye from aqueous solution. The as-synthesized MCM-41 was calcined at 250 and 550°C to study the relation between the surface area and pore volume with surfactant removal. The synthesized MCM-41 was characterized using thermo gravimetric analysis (TGA), X-ray diffraction (XRD) patterns, nitrogen adsorption/desorption isotherms and Fourier transform infrared (FT-IR) spectroscopy. The MCM-41 calcined at 550°C showed higher surface area (1,059 m² g^?1) with pore volume of 0.89 ml g^?1 and was used for the investigation of adsorption isotherms and kinetics. The experimental results indicated that the Freundlich and Redlich-Peterson models expressed the adsorption isotherm better than the Langmuir model. In addition, the influence of temperature and pH on adsorption was also investigated. The decrease in temperature or the increase in pH enhanced the adsorption of dye onto MCM-41. A maximum adsorption capacity of 1.5×10^?4 mol g^?1 was obtained at 30°C. The kinetic studies showed that the adsorption of dye on MCM-41 follows the pseudo-second-order kinetics.     

Adsorption and kinetic studies of methylene blue on modified HUSY zeolite and an amorphous mixture of γ-alumina and silica

ABSTRACT

Our work focuses on the study of the adsorption of methylene blue (MB) on adsorbents based on zeolite HUSY and (γAl₂O₃-SiO₂). To optimize the process of removing MB onto Ni/Co USY, different parameters were studied such as contact time, initial pH, initial dye concentration, zero charge’s point, and adsorbent dosage. The adsorption isotherm follows the Langmuir model. The maximum adsorption capacities of MB were 59.88 mg g^?1 for Ni/Co USY and 43.86 mg g^?1 for Ni/Co (γAl-Si) at 298°K. The thermodynamic parameters and activation energy’s values obtained suggested that the adsorption was a physical process, spontaneous, and endothermic in nature. MB adsorption on Ni/Co USY may occur via electrostatic interaction, hydrogen bonding, and Lewis acid–base interaction.