Efficient adsorption of radioactive iodine by covalent organic framework/chitosan aerogel.

Radioactive iodine is considered one of the most dangerous radioactive elements in nuclear waste. Therefore, effective capture of radioactive iodine is essential for developing and using nuclear energy to solve the energy crisis. Some materials that have been developed for removing radioactive iodine still suffer from complex synthesis, low removal capacity, and non-reusability. Herein, covalent organic framework (COF)/chitosan (CS) aerogels were prepared using vacuum freeze-drying, and the COF nanoparticles were tightly attached on the green biomass material CS networks. Due to the synergistic effect of both COF and CS, the composite aerogel shows a three-dimensional porous and stable structure in the recycle usage. The COF/CS aerogel exhibits excellent iodine adsorption capacity of 2211.58 mg g-1 and 5.62 g g-1 for static iodine solution and iodine vapor, respectively, better than some common adsorbents. Furthermore, COF/CS aerogel demonstrated good recyclability performance with 87 % of the initial adsorption capacity after 5 cycles. In addition, the interaction between iodine and imine groups, amino groups, and benzene rings of aerogel are the possible adsorption mechanisms. COF/CS aerogel has excellent adsorption properties, good chemical stability, and reusable performance, which is a potential and efficient adsorbent for industrial radioactive iodine adsorption from nuclear waste.

High-efficient removal of anionic dye from aqueous solution using metal-organic frameworks@chitosan aerogel rich in benzene structure.

With the exponentially increase of dye pollutants, the purification of dye wastewater has been an urgent ecological problem. As a novel type of porous adsorbent, metal-organic frameworks still face challenges in recyclability, agglomeration, and environmentally unfriendly synthesis. Herein, MOF-525 was in-situ growth onto the surface of the chitosan (CS) beads to fabricate MOF-525@CS aerogel. CS was utilized as substrate to uniformly disperse MOF-525, thereby significantly mitigating agglomeration and improving recyclability of MOF-525. The characterization results shown that MOF-525@CS aerogel had a high specific surface area of 103.0 m2·g-1, and MOF-525 was uniformly distributed in the 3D porous structure of CS, and the presence of benzoic acid was detected. The MOF-525@CS aerogel had a remarkable adsorption capacity of 1947 mg·g-1 for Congo red, which is greater than the sum of its parts. MOF-525@CS aerogel also inherited the rapid adsorption ability of MOF-525, removing 80 % of Congo red within 600 min. Such excellent adsorption performance can be attributed to the benzoic acid trapped by CS via CN band to enhance the π-π stacking interactions. Additionally, the utilization of benzoic acid makes the synthesis process of MOF-525@CS aerogel more environmentally friendly. The high-efficient MOF-525@CS aerogel is a competitive candidate for dye pollution adsorption.

Porous metal-organic framework-acrylamide-chitosan composite aerogels: Preparation, characterization and adsorption mechanism of azo anionic dyes adsorbed from water.

Micro- and nano-metal-organic frameworks with different adsorption properties were prepared by a time-modulation hydrothermal method. By comparing the adsorption properties, the most effective MIL-68(Fe)-12 was selected to be mixed with chitosan (CS), and porous metal-organic framework-acrylamide-chitosan composite aerogel (PMACA) was prepared by introducing acrylamide prior to glutaraldehyde crosslinking. The adsorption capacity of PMACA doped with acrylamide was as high as 2086.44 mg·g-1. The adsorption performance of PMACA was 1.48 times higher compared to the porous metal-organic framework-chitosan composite aerogel (PMCA) undoped with acrylamide. With the introduction of acrylamide, the stability of PMACA was improved, making it less prone to dispersion and decomposition. Structural characterization and adsorption properties were analyzed using methods such as XRD, FTIR, TGA, SEM, BET, and Zeta potential. The adsorption performance of PMACA was investigated further through batch tests with variables such as adsorbent dosage, pH, contact time, initial CR solution concentration, and temperature. The model fitting of PMACA was consistent with the pseudo-second-order model and the Sips model. The adsorption thermodynamics showed that high temperature promoted spontaneous adsorption behavior. PMACA showed a recovery rate of approximately 86 % after six cyclic adsorption tests. PMACA maintained a recovery rate of roughly 86 % after six cyclic adsorption tests. The combined effects of electrostatic attraction, hydrogen bonding, and π-π conjugation resulted in excellent adsorption performance, while pore filling also contributed to the efficient adsorption of Congo red (CR).

Green preparation of magnetic ferroferric oxide-polyvinyl alcohol-alginate coated UiO-67 nanospheres: Characterization, adsorption properties and adsorption mechanism of methylene blue.

In this paper, a kind of magnetic ferric oxide/polyvinyl alcohol/calcium alginate/UiO-67 (Fe3O4/PVA/CA/UiO-67) nanospheres with homogeneous surface interconnecting structures was prepared by using macromolecular polymer polyvinyl alcohol and sodium alginate as carriers and zirconium organic skeleton as nanocrystals. The properties of magnetic nanospheres were studied by SEM, FT-IR, TGA, XRD, BET, VSM and Zeta potential. The impression of diverse temperatures, MB concentrations, interaction time, pH, and magnetic aerogel sphere dose on MB removal was studied. The optimum adsorption temperature and pH of magnetic nanospheres for MB were 298 K, and 10, respectively. Langmuir simulated that the maximum removal of MB by magnetic nanospheres at room temperature (298 K) was 1371.8 mg/g. The removal of MB by magnetic nanospheres complied with the pseudo-first-order kinetic model. The isotherm simulation can infer that the Langmuir model was more comply with MB adsorption on magnetic aerogel spheres. Thermodynamic studies have confirmed that the removal of MB by magnetic nanospheres was exothermic and spontaneous. The interaction mechanism of MB on magnetic nanospheres can be deduced by FT-IR and BET, including hydrogen bond, π-π bond, electrostatic interaction, and mesoporous pore flow. The removal rate of nanospheres for MB still reached 70.06 % after six cycles.

Efficient adsorption of methylene blue in water by nitro-functionalized metal-organic skeleton­calcium alginate composite aerogel.

This paper presents the first investigation of the adsorption performance of methylene blue by the nitro-functionalized metal-organic framework (MIL-88B-NO2). MIL-88B-NO2 has a specific surface area of 836.0 m2/g, which is 109.8 % higher than MIL-88B. The maximum adsorption capacity of methylene blue is 383.6 mg/g, which is 68.2 % higher than that of MIL-88B. This phenomenon can be attributed to the great increase in specific surface area and the introduction of nitro-functional groups. However, its microcrystalline nature makes it difficult to remove in practical applications and quickly causes secondary pollution. Therefore, the composite of MIL-88B-NO2 and calcium alginate (CA) to form aerogel maintains the inherent properties of the two materials and makes it easy to recycle. The utmost adsorption capability of MIL-88B-NO2/CA-2 aerogel is 721.0 mg/g. Compared with MIL-88B-NO2, the adsorption performance of MIL-88B-NO2/CA-2 aerogel is further improved by 88.0 %. The higher adsorption capacity of the adsorbent may be due to the synergistic interplay of electrostatic attraction, π-π conjugation, hydrogen bonding, metal coordination effect, and physicochemical properties. Also, MIL-88B-NO2/CA-2 aerogel has good recyclability, indicating that it has broad application prospects in the removal of positive dyes in contaminated water.

Efficient adsorption of azo anionic dye Congo Red by micro-nano metal-organic framework MIL-68(Fe) and MIL-68(Fe)/chitosan composite sponge: Preparation, characterization and adsorption performance.

Micro-nano metal-organic framework (MIL-68(Fe)) for efficient adsorption of azo anionic dye Congo red (CR) was successfully prepared by one-step hydrothermal method under acidic environment. And a MIL-68(Fe)/chitosan composite sponge (MIL-68(Fe)/CS) was prepared under the coating of chitosan (CS). After comparing the performance of MIL-68(Fe) and MIL-68(Fe)/CS, we focus on exploring MIL-68(Fe)/CS. It ensured the CR removal efficiency while reaching the adsorption equilibrium faster than MIL-68(Fe), and solved the defect that the powder was difficult to be stripped by water after adsorption. The physicochemical properties and surface morphology of the adsorbent were characterized by SEM, FTIR, XRD, TGA, BET, and Zeta potential. The effects of pH, contact time, adsorbent dosage, initial solution concentration and temperature on the adsorption performance of the adsorbent were systematically analyzed. The pseudo-second-order model and the Sips model were most consistent for the adsorption process, indicating that the adsorption process of MIL-68(Fe)/chitosan composite sponge on CR is a complex physicochemical process. The removal rates of CR by MIL-68(Fe) and MIL-68(Fe)/chitosan composite sponge reached the maximum values of 99.55 % and 99.51 % at 318 K, respectively. And the maximum adsorption capacity of CR by MIL-68(Fe)/chitosan composite sponge at 318 K was 1184.16 mg·g-1. After six cycles of adsorption and desorption, the removal rate of CR was still higher than 80 %. The synergistic effects of π-π stacking, electrostatic interactions, hydrogen bonding and pore filling have important effects on CR removal.

The Defects, Physicochemical Properties, and Surface Charge of MIL-88A (Al) Crystal Were Regulated for Highly Efficient Removal of Anionic Dyes: Preparation, Characterization, and Adsorption Mechanism.

In this paper, the physicochemical properties, surface charge, and crystal defects of MIL-88A (Al) were controlled by adjusting the ratio of metal ligands and temperature in the synthetic system without the addition of surfactants. The adsorption properties of different crystals for Congo red (CR) were studied. Among them, MIL-88A (Al)-130 and MIL-88A (Al)-d have the best adsorption properties. The maximum adsorption capacities are 600.8 and 1167 mg · g-1, respectively. Compared with MIL-88A (Al)-130, the adsorption performance of MIL-88A (Al)-d was increased by 94.2%, and the adsorption rate was increased by about 4 times. It can be seen that increasing the proportion of metal ligands within a certain range will improve the adsorption capacity. The structure and morphology of the adsorbent were characterized by XRD, FTIR, SEM, EDS, TGA, BET, and zeta potential. The effects of time, temperature, pH, initial solution concentration, and dosage on CR adsorption properties were systematically discussed. The pseudo-second-order kinetic model and Langmuir isothermal model can well describe the adsorption process, which indicates that the adsorption process is a single-layer chemisorption occurring on a uniform surface. According to thermodynamics, this adsorption is an endothermic process. The mechanism of CR removal is proposed as the electrostatic attraction, hydrogen bond, metal coordination effect, π-π conjugation, crystal defect, and pore-filling effect. In addition, MIL-88A (Al)-d has good repeatability, indicating that it is a good material for treating anionic dye wastewater.

NiFe Nanoparticle-Encapsulated Ultrahigh-Oxygen-Doped Carbon Layers as Bifunctional Electrocatalysts for Rechargeable Zn-Air Batteries.

There is an urgent demand for developing highly efficient bifunctional electrocatalysts with excellent stability toward the oxygen evolution and reduction reactions (OER and ORR, respectively) for rechargeable Zn-air batteries (ZABs). In this work, NiFe nanoparticles encapsulated within ultrahigh-oxygen-doped carbon quantum dots (C-NiFe) as bifunctional electrocatalysts are successfully obtained. The accumulation of carbon layers formed by carbon quantum dots results in abundant pore structures and a large specific surface area, which is favorable for improving catalytic active site exposure, ensuring high electronic conductivity and stability simultaneously. The synergistic effect of NiFe nanoparticles enriched the number of active centers and naturally increased the inherent electrocatalytic performance. Benefiting from the above optimization, C-NiFe shows excellent electrochemical activity for both OER and ORR processes (the OER overpotential is only 291 mV to achieve 10 mA cm-2). Furthermore, the C-FeNi catalyst as an air cathode displays an impressive peak power density of 110 mW cm-2, an open-circuit voltage of 1.47 V, and long-term durability over 58 h. The preparation of this bifunctional electrocatalyst provides a design idea for the construction of bimetallic NiFe composites for high-performance Zn-air batteries.

The therapeutic role and potential mechanism of EGCG in obesity-related precocious puberty as determined by integrated metabolomics and network pharmacology.

Objective: (-)-Epigallocatechin-3-gallate (EGCG) has preventive effects on obesity-related precocious puberty, but its underlying mechanism remains unclear. The aim of this study was to integrate metabolomics and network pharmacology to reveal the mechanism of EGCG in the prevention of obesity-related precocious puberty. Materials and methods: A high-performance liquid chromatography-electrospray ionization ion-trap tandem mass spectrometry (LC-ESI-MS/MS) was used to analyze the impact of EGCG on serum metabolomics and associated metabolic pathways in a randomized controlled trial. Twelve weeks of EGCG capsules were given to obese girls in this trail. Additionally, the targets and pathways of EGCG in preventing obesity-related precocious puberty network pharmacology were predicted using network pharmacology. Finally, the mechanism of EGCG prevention of obesity-related precocious puberty was elucidated through integrated metabolomics and network pharmacology. Results: Serum metabolomics screened 234 endogenous differential metabolites, and network pharmacology identified a total of 153 common targets. These metabolites and targets mainly enrichment pathways involving endocrine-related pathways (estrogen signaling pathway, insulin resistance, and insulin secretion), and signal transduction (PI3K-Akt, MAPK, and Jak-STAT signaling pathways). The integrated metabolomics and network pharmacology indicated that AKT1, EGFR, ESR1, STAT3, IGF1, and MAPK1 may be key targets for EGCG in preventing obesity-related precocious puberty. Conclusion: EGCG may contribute to preventing obesity-related precocious puberty through targets such as AKT1, EGFR, ESR1, STAT3, IGF1, and MAPK1 and multiple signaling pathways, including the estrogen, PI3K-Akt, MAPK, and Jak-STAT pathways. This study provided a theoretical foundation for future research.

Simple synthesis of chitosan/alginate/graphene oxide/UiO-67 amphoteric aerogels: Characterization, adsorption mechanism and application for removal of cationic and anionic dyes from complex dye media.

A chitosan/alginate/graphene oxide/UiO-67 (CS/SA/GO/UiO-67) amphoteric aerogel was synthesized successfully. A series of characterization experiments of CS/SA/GO/UiO-67 amphoteric aerogel was performed by SEM, EDS, FT-IR, TGA, XRD, BET, and zeta potential. The competitive adsorption properties of different adsorbents for complex dyes wastewater (MB and CR) at room temperature (298 K) were compared. Langmuir isotherm model predicted that the maximum adsorption quantity of CS/SA/GO/UiO-67 for CR and MB was 1091.61 and 1313.95 mg/g, respectively. The optimum pH values of CS/SA/GO/UiO-67 for the adsorption of CR and MB were 5 and 10, respectively. The kinetic analysis showed that the adsorption of MB and CR on CS/SA/GO/UiO-67 was more suitable for the pseudo-second-order and pseudo-first-order kinetic model, respectively. The isotherm study revealed that the adsorption of MB and CR was consistent with the Langmuir isotherm model. The thermodynamic study demonstrated that the adsorption process of MB and CR was exothermic and spontaneous. FT-IR analysis and zeta potential characterization experiments revealed that the adsorption mechanism of MB and CR on CS/SA/GO/UiO-67 depended on π-π bond, hydrogen bond, and electrostatic attraction. Repeatable experiments showed that the removal rates of MB and CR of CS/SA/GO/UiO-67 after six cycles of adsorption were 67.19 and 60.82 %, respectively.

Enhanced methylene blue adsorption using zirconate alginate/graphene oxide/UiO-67 aerogel spheres: Synthesis, characterization, kinetic studies, and adsorption mechanisms.

Zirconium alginate/graphene oxide (ZA/GO) hydrogel spheres were prepared by crosslinking sodium alginate and GO with Zr4+. Then Zr4+ on the surface of the ZA/GO substrate acted as the metal nucleation site of the UiO-67 crystal and interacted with the organic ligand biphenyl 4-4'-dicarboxylic acid (BPDC) to make UiO-67 grow in situ on the surface of the ZA/GO hydrogel sphere by the hydrothermal method. The BET surface areas of ZA/GO, ZA/UiO-67, and ZA/GO/UiO-67 aerogel spheres were 1.29, 47.71, and 89.33 m2/g respectively. The maximum adsorption capacities of ZA/GO, ZA/UiO-67, and ZA/GO/UiO-67 aerogel spheres for methylene blue (MB) at room temperature (298 K) were 145.08, 307.49, and 1105.23 mg/g respectively. The kinetic analysis showed that the adsorption process of MB on the ZA/GO/UiO-67 aerogel sphere was consistent with the pseudo-first-order kinetic model. Isotherm analysis showed that MB was adsorbed on ZA/GO/UiO-67 aerogel spheres as a single layer. Thermodynamic analysis showed that the adsorption process of MB on the ZA/GO/UiO-67 aerogel sphere was exothermic and spontaneous. Adsorption of MB on ZA/GO/UiO-67 aerogel spheres is mainly dependent on π-π bond, electrostatic interaction, and hydrogen bond. After 8 cycles, ZA/GO/UiO-67 aerogel spheres still showed high adsorption performance and good reuse ability.

Efficient adsorption of Congo red by micro/nano MIL-88A (Fe, Al, Fe-Al)/chitosan composite sponge: Preparation, characterization, and adsorption mechanism.

MIL-88A crystals with three different metal ligands (Fe, Al, FeAl) were prepared by hydrothermal method for the first time. The three materials' crystal structure and surface morphology are different, leading to different adsorption properties of Congo red (CR). The maximum adsorption capacities of MIL-88A (Fe), MIL-88A (FeAl), and MIL-88A (Al) are 607.7 mg · g-1, 536.4 mg · g-1, and 512.1 mg · g-1 respectively. In addition, MIL-88A was combined with chitosan (CS) respectively, and MIL-88A/CS composite sponge was prepared by the freeze-drying method, which not only solved the defect that MIL-88A powder was difficult to recover but also further improved the removal ability of CR by the adsorbent. The maximum adsorption capacities of MIL-88A (FeAl)/CS, MIL-88A (Fe)/CS, MIL-88A (Al)/CS, and CS are 1312 mg · g-1, 1056 mg · g-1, 996.7 mg · g-1, and 769.6 mg · g-1, respectively. The structure and physicochemical properties of the materials were analyzed by SEM, FTIR, XRD, TGA, BET, and Zeta. The adsorption process of CR follows pseudo-second-order kinetics and Langmuir, Sips isotherm model. Combined with thermodynamic parameters, the adsorption behavior was described as endothermic monomolecular chemical adsorption. The removal of CR is attributed to electrostatic interactions, hydrogen bonding, metal coordination effects, and size-matching effects.

Removal of Methylene Blue Dye from Aqueous Solutions by Pullulan Polysaccharide/Polyacrylamide/Activated Carbon Complex Hydrogel Adsorption.

In this study, composite hydrogels were prepared using a simple synthetic technique to adsorb methylene blue (MB) from water. The hydrogel comprised potassium persulfate (KPS) as the initiator, N,N'-methylene bisacrylamide as the crosslinking agent, and sodium hydroxide (NaOH) as the activator. It was employed to adsorb MB at different concentrations from water. The morphology and properties of PUL/PAM/GO composites were characterized through thermogravimetric analysis, Fourier transform infrared spectroscopy, and scanning electron microscopy. Moreover, the adsorption properties, adsorption isotherms, adsorption kinetics, adsorption thermodynamics, and swelling properties of the hydrogel for MB were investigated. The optimal ratio of PUL to AC was obtained as 6:1 by fixing the amount of PUL and loading AC of different masses. The maximum adsorption capacity was obtained as 591.4 mg/g. It also exhibited certain mechanical strength. The adsorption of MB conforms to pseudo-first-order kinetics and Langmuir isotherms. In this study, an environment-friendly, cheap, simple, and efficient way was presented for the composite hydrogel in the direction of water treatment.

Methylene Blue Removed from Aqueous Solution by Encapsulation of Bentonite Aerogel Beads with Cobalt Alginate.

It can be difficult to remove dark methylene blue (MB) from water effectively. The use of sodium alginate and bentonite (Ben) as the matrix produced a displacement reaction that occurred in cobalt chloride, which allowed Ben to be successfully encapsulated in cobalt alginate (CA). Finally, a vacuum freeze-drying method was used to prepare a low-cost composite of CA/Ben aerogel for adsorbing MB in aqueous solutions. In addition to scanning electron microscopy, thermogravimetric analysis, and Fourier transform infrared spectroscopy, the composites were also characterized and analyzed. Different adsorption experiments were conducted in order to determine the effects of dosage, pH, adsorption time, and temperature on the adsorption performance of the adsorbent. According to the results of the experiment, the adsorption capacity of CA/Ben aerogel was 258.92 mg·g-1, and the pseudo-first-order kinetic model and Freundlich isotherm model can fully explain the adsorption process of MB on this aerogel. The composite material reported in this paper is easily recycled, and the removal rate reaches 65% after four times of recycling. Moreover, compared with other adsorbents, the composite material of the invention is highly environmentally friendly and has a simple preparation process. A large-scale application of this technology is the removal of dyes from water on a large scale.

Effective Removal of Tetracycline from Water Using Copper Alginate @ Graphene Oxide with In-Situ Grown MOF-525 Composite: Synthesis, Characterization and Adsorption Mechanisms.

For nanomaterials, such as GO and MOF-525, aggregation is the main reason limiting their adsorption performance. In this research, Alg-Cu@GO@MOF-525 was successfully synthesized by in-situ growth of MOF-525 on Alg-Cu@GO. By dispersing graphene oxide (GO) with copper alginate (Alg-Cu) with three-dimensional structure, MOF-525 was in-situ grown to reduce aggregation. The measured specific surface area of Alg-Cu@GO@MOF-525 was as high as 807.30 m2·g-1, which is very favorable for adsorption. The synthesized material has affinity for a variety of pollutants, and its adsorption performance is significantly enhanced. In particular, tetracycline (TC) was selected as the target pollutant to study the adsorption behavior. The strong acid environment inhibited the adsorption, and the removal percentage reached 96.6% when pH was neutral. Temperature promoted the adsorption process, and 318 K adsorption performance was the best under experimental conditions. Meanwhile, 54.6% of TC could be removed in 38 min, and the maximum adsorption capacity reached 533 mg·g-1, far higher than that of conventional adsorption materials. Kinetics and isotherms analysis show that the adsorption process accords with Sips model and pseudo-second-order model. Thermodynamic study further shows that the chemisorption is spontaneous and exothermic. In addition, pore-filling, complexation, π-π stack, hydrogen bond and chemisorption are considered to be the causes of adsorption.

Removal of Methylene Blue by Crosslinked Egg White Protein/Graphene Oxide Bionanocomposite Aerogels.

Egg white protein is a non-toxic and biodegradable biopolymer that forms a gel easily via simple thermal denaturation treatment. A novel aerogel on the basis of egg white protein crosslinked with graphene oxide was prepared via a facile freeze-drying method. The structure and physicochemical characteristics of the aerogels were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA) and Brunauer-Emmett-Teller (BET) analysis. The adsorption properties of the aerogels were investigated by studying the influencing factors such as the solution pH, dose, temperature and contact time. The adsorption capacity of methylene blue onto the aerogels was tested, whose maximum adsorption capacity, calculated by the Langmuir isotherm equation, reached 91.7 mg/g. Adsorption kinetics studies showed that the adsorption followed the pseudo-second-order kinetic model. Thermodynamic data implied that methylene blue adsorbed by the aerogels was an exothermic and spontaneous process.

Study on the Adsorption Performance of Casein/Graphene Oxide Aerogel for Methylene Blue.

Casein (CS) and graphene oxide (GO) were employed for the fabrication of a casein/graphene oxide (CS/GO) aerogel by vacuum freeze drying. Fourier transform infrared spectroscopy, scanning electron microscopy, surface area and micropore analysis (BET), and thermogravimetric analysis were used to characterize the specific surface area, structure, thermal stability, and morphology of the CS/GO aerogel. The influence of experimental parameters such as the GO mass fraction in the aerogel, metering of the adsorbent, pH, contact time, and temperature on the adsorption capacity of the CS/GO aerogel on methylene blue (MB) was also investigated. According to Langmuir isotherm determination, the maximum removal rate of MB from the CS/GO aerogel was 437.29 mg/g when the temperature was 293 K and pH was 8. Through kinetic and thermodynamic studies, it is found that adsorption follows a pseudo-second-order reaction model and is also an exothermic and spontaneous process.

One-step generation of S and N co-doped reduced graphene oxide for high-efficiency adsorption towards methylene blue.

S and N co-doped reduced graphene (S-N-rGO) nanohybrids were prepared by a one-step oil bath heating process using glutathione (GSH) as a green and mild co-reduction agent and a S and N source. It can be applied in the field of adsorption for the removal of methylene blue (MB) from aqueous solutions. The efficient adsorption rate of S-N-rGO hybrids for MB (50 mg L-1) was observed with the best even within 2'07'' from blue solutions into colorless (the mass ratio GO : GSH = 60 : 200). Under this mass ratio, the effects of initial solution pH, temperature, initial concentration and contact time on adsorption towards MB were explored systematically. The results indicated that the adsorption capacity at 275 K could reach up to 598.8 mg g-1, the adsorption behavior followed the pseudo-second-order kinetic model and the equilibrium adsorption data fitted the Langmuir isotherm well. Thermodynamic and kinetic analyses revealed that adsorption is an exothermic, spontaneous and physisorption process.

ZnCl2-activated carbon from soybean dregs as a high efficiency adsorbent for cationic dye removal: isotherm, kinetic, and thermodynamic studies.

Activated carbon was prepared from soybean dregs using chemical activation by zinc chloride. The influence of activation parameters such as impregnation ratio, activation temperature and carbonization time was investigated. The physicochemical properties of activated carbon were characterized using SEM, FTIR, BET and TGA, respectively. The effect factors including pH, contact time, temperature and dose on the adsorption properties of methylene blue onto activated carbon were studied. The adsorption equilibrium data of methylene blue onto activated carbon were well fitted to the Langmuir model, giving a maximum adsorption capacity of 255.10 mg/g. It indicates that activated carbon is a promising adsorbent for removing methylene blue from aqueous solution. The kinetic data were well described by the pseudo-second-order model. Thermodynamic parameters indicate that adsorption process is spontaneous and endothermic.The effect of temperature on MB adsorbed by AC shows that the equilibrium adsorption capacity increases with increasing temperature from 303 to 323 K. Increasing adsorption capacities with temperature indicate that the adsorption of MB onto AC is controlled by an endothermic reaction.

Preparation of improved gluten material and its adsorption behavior for congo red from aqueous solution.

Improved gluten materials were prepared using bio-fermentation and acid bath coagulation methods for congo red adsorption. After comparison, the method of acid bath coagulation with better effect was selected and further preparations of improved gluten materials were achieved under different acid coagulation baths and the solid-liquid ratios. Finally, particular adsorption properties were studied using the sample of improved gluten material with the acid coagulation bath of HCl and the solid-liquid ratio of 1:5. Influence parameters on the congo red adsorption such as temperature, dose, contact time and pH were discussed. The adsorption properties of the improved gluten material were investigated by isotherm (the Langmuir model and the Freundlich model), kinetics (the pseudo-first-order, pseudo-second-order and intra-particle diffusion equations) and thermodynamic analysis. The results showed that this improved gluten material was an efficient adsorbent for removal of congo red.