Removal of Cr (VI) by Biochar Derived from Six Kinds of Garden Wastes: Isotherms and Kinetics

Garden waste is one of the main components of urban solid waste which affects the urban environment. In this study, garden waste of Morus alba L. (SS), Ulmus pumila L. (BY), Salix matsudana Koidz (LS), Populus tomentosa (YS), Sophora japonica Linn (GH) and Platycladus orientalis (L.) Franco (CB) was pyrolyzed at 300 °C, 500 °C, 700 °C to obtain different types of biochar, coded as SSB300, SSB500, SSB700, BYB300, etc., which were tested for their Cr (VI) adsorption capacity. The results demonstrated that the removal efficiency of Cr by biochar pyrolyzed from multiple raw materials at different temperatures was variable, and the pH had a great influence on the adsorption capacity and removal efficiency. GHB700 had the best removal efficiency (89.44%) at a pH of 2 of the solution containing Cr (VI). The pseudo second-order kinetics model showed that Cr (VI) adsorption by biochar was chemisorption. The Langmuir model showed that the adsorption capacity of SSB300 was the largest (51.39 mg·g⁻¹), BYB500 was 40.91 mg·g⁻¹, GHB700, CBB700, LSB700, YSB700 were 36.85 mg·g⁻¹, 36.54 mg·g⁻¹, 34.53 mg·g⁻¹ and 32.66 mg·g⁻¹, respectively. This research, for the first time, used a variety of garden wastes to prepare biochar, and explored the corresponding raw material and pyrolysis temperature for the treatment of Cr (VI). It is hoped to provide a theoretical basis for the research and utilization of garden wastes and the production and application of biochar.     

Removal Performance and Mechanism of Benzo(b)Fluorathene Using MnO2 Nanoflower/Graphene Oxide Composites

High-ring polycyclic aromatic hydrocarbons (PAHs, Benzo[b]fluorathene (BbFA), etc.) are difficult to biodegrade in the water environment. To address this issue, an innovative method for the preparation of MnO₂ nanoflower/graphene oxide composite (MnO₂ NF/GO) was proposed for adsorption removal of BbFA. The physicochemical properties of MnO₂ NF/GO were characterized by SEM, TEM, XRD, and N₂ adsorption/desorption and XPS techniques. Results show that the MnO₂ NF/GO had well-developed specific surface area and functional groups. Batch adsorption experiment results showed that adsorption capacity for BbFA was 74.07 mg/g. The pseudo-second-order kinetic model and Freundlich isotherm model are fitted well to the adsorption data. These show electron-donor-acceptor interaction; especially π-π interaction and π complexation played vital roles in BbFA removal onto MnO₂ NF/GO. The study highlights the promising potential adsorbent for removal of PAHs.     

Development of Efficient Photocatalyst MIL-68(Ga)_NH2 Metal-Organic Framework for the Removal of Cr(VI) and Cr(VI)/RhB from Wastewater under Visible Light

Severe environmental pollution is caused by the massive discharge of complex industrial wastewater. The photocatalytic technology has been proved as an effective way to solve the problem, while an efficient photocatalyst is the most critical factor. Herein, a new photocatalyst MIL-68(Ga)_NH₂ was obtained by hydrothermal synthesis and were characterized by PXRD, FTIR, ¹H NMR, and TGA systematically. The result demonstrates that MIL-68(Ga)_NH₂ crystallized in orthorhombic system and Cmcm space group with the unit cell parameters: a = 36.699 Å, b = 21.223 Å, c = 6.75 Å, V = 5257.6 ų, which sheds light on the maintenance of the crystal structure of the prototype material after amino modification. The conversion of Cr(VI) and binary pollutant Cr(VI)/RhB in wastewater under visible light stimulation was characterized by the UV-vis DRS. Complementary experimental results indicate that MIL-68(Ga)_NH₂ exhibits remarkable photocatalytic activity for Cr(VI) and the degradation rate reaches as high as 98.5% when pH = 2 and ethanol as hole-trapping agent under visible light irradiation with good reusability and stability. Owing to the synergistic effect between Cr(VI) and RhB in the binary pollutant system, MIL-68(Ga)_NH₂ exhibits excellent catalytic activity for both the pollutants, the degradation efficiency of Cr(VI) and RhB was up to 95.7% and 94.6% under visible light irradiation for 120 min, respectively. The possible removal mechanism of Cr(VI)/RhB based on MIL-68(Ga)_NH₂ was explored. In addition, Ga-based MOF was applied in the field of photocatalytic treatment of wastewater for the first time, which broadened the application of MOF materials in the field of photocatalysis.     

Removal of Chromium(VI) from Aqueous Solutions Using Fe3O4 Magnetic Polymer Microspheres Functionalized with Amino Groups

Magnetic polymer microspheres (MPMs) using glycidylmethacrylate (GMA) as a functional monomer were synthesized in the presence of Fe₃O₄ nanoparticles via dispersion polymerization. After polymerization, the magnetic polymer microbeads were modified with ethylenediamine (EDA). The obtained ethylenediamine-functionalized magnetic microspheres (EDA-MPMs) were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD), vibrating-sample magnetometer (VSM) and Fourier transform infrared (FT-IR) spectroscopy. Then the EDA-MPMs were applied as adsorbents for the removal of Cr(VI) from aqueous solution. Langmuir equation was appropriate to describe the experimental data. The maximum adsorption capacities obtained from the Langmuir model were 236.9, 242.1 and 253.2 mg/g at 298, 308 and 318 K, respectively. The Cr(VI) adsorption equilibrium was established within 120 min and the adsorption kinetics was compatibly described by the pseudo-second order equation. The thermodynamic parameters (ΔG°, ΔH°, ΔS°) of the sorption process revealed that the adsorption was spontaneous and was an endothermic process. The regeneration study demonstrated that the EDA-MPMs could be repeatedly utilized with no significant loss of adsorption efficiency.     

Fixed-Bed Modification of Zeolitic Tuffs and Their Application for Cr(VI) Removal

Natural clinoptilolite tuff (CL) and chabazite-clinoptilolite tuff (CH) were modified in fixed-bed column by immobilization of hexadecyltrimethylammonium bromide (HDTMA-Br), then investigated as a sorbent for inorganic anions of Cr(VI). The proposed modification technique combined with surfactant solution batching allows minimizing the surfactant loses through foaming and crystallization and creation of stable organic coverage. The HDTMA loading depended on the mineral composition of the zeolitic tuff, the topology of its external surface, and process conditions. The maximum surface coverage was obtained by gradually dosing surfactant solution in the smallest volume of batches and corresponded up to 100% and 182% of external cation exchange capacity (ECEC) for mono and double layer coverage, respectively. In case of mono layer coverage, modification proceeds until the exhaustion of surfactant in supply solution, while in the double layer one, until equilibrium of HDTMA concentration in both zeolitic and liquid phases was established. The efficiency of Cr(VI) uptake by prepared surface modified zeolites (SMZs) increased with increasing of HDTMA loading. In the case of mono layer SMZs, the capacities of CH-HDTMA and CL-HDTMA were 10.3 and 5.4 mg/g, respectively, while in the case of double layer SMZs, the amount of Cr uptake on CH-HDTMA and CL-HDTMA were 16.8 and 15 mg/g, respectively. Ion exchange is the predominant mechanism of Cr(VI) sorption but it takes place only if modification resulted in at least partial double layer coverage. The XPS analysis reveals Cr(VI) reduction to a less-toxic Cr(III) by the electron donating N-containing groups and by reaction with Fe⁺² ions on the zeolite external surface.     

Crown-Ether-Modified SBA-15 for the Adsorption of Cr(VI) and Zn(II) from Water

Recently, the release of some metal ions to the environment has been observed to cause serious damages to human health and the environment. Herein, a chromium(VI)- and zinc(II)-selective adsorbent (CB18crown6/SBA-15) was successfully fabricated through the covalent attachment of 4′-carboxybenzo-18-crown-6 (CB18crown6) as a ligand on mesoporous silica support (SBA-15). The CB18crown6/SBA-15 adsorbent was characterized by Fourier-transform infrared (FTIR) spectrometry, X-ray diffraction (XRD), N₂ adsorption–desorption, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). To evaluate its ability to selectively capture Cr(VI) and Zn(II), adsorption experiments were conducted. The influences of pH, initial concentration of metal ions, and coexisting metal ions on the adsorption process were examined. The CB18crown6/SBA-15 selectively adsorbed Cr(VI) at pH 2 and Zn(II) at pH 5, respectively, from the mixed aqueous solutions of chromium, zinc, lithium, cadmium, cobalt, strontium, and cesium ions. The data for the adsorption of Cr(VI) onto the CB18crown6/SBA-15 were well explained by the Langmuir adsorption isotherm. In addition, the recycling and reuse of CB18crown6/SBA-15 was successfully achieved, and 71 and 76% reuse efficiency of Cr(VI) and Zn(II), respectively, was obtained after five cycles. This study suggests that the use of the CB18crown6/SBA-15 can be a feasible approach for the selective remediation of Cr(VI) and Zn(II) contamination.     

Chemical Modification of Chitosan for Removal of Pb(II) Ions from Aqueous Solutions

Biomacromolecule have a significant contribution to the adsorption of metal ions. Moreover, chitosan is one of the most studied biomacromolecule, which has shown a good performance in the field of wastewater treatment. In this context, a new adsorbent of the aminophosphonic modified chitosan-supported Ni(II) ions type was prepared from the naturally biopolymer, chitosan. In the first step, modified chitosan with aminophosphonic acid groups was prepared using the “one-pot” Kabachnik-Fields reaction. It was characterized by different techniques: FTIR, SEM/EDAX, TGA, and ³¹P-NMR. In the second step, the modified chitosan with aminophosphonic acid was impregnated with Ni(II) ions using the hydrothermal reaction at different values of pH (5, 6 and 7). The physical-chemical characteristics of final products (modified chitosan carrying aminophosphonic groups and Ni(II) ions) were investigated using FTIR, SEM images, EDAX spectra and thermogravimetric analysis. In this work, the most important objective was the investigation of the adsorbent performance of the chitosan modified with aminophosphonic groups and Ni(II) ions in the process of removing Pb(II) ions from aqueous solutions by studying the effect of pH, contact time, and Pb(II) ions concentration. For removal of Pb(II) ions from the aqueous solution, the batch adsorption method was used.     

Fabrication of MNPs/rGO/PMMA Composite for the Removal of Hazardous Cr(VI) from Tannery Wastewater through Batch and Continuous Mode Adsorption

Herein, we report the synthesis of magnetic nanoparticle (MNP)-reduced graphene oxide (rGO) and polymethylmethacrylate (PMMA) composite (MNPs/rGO/PMMA) as adsorbent via an in situ fabrication strategy and, in turn, the application for adsorptive removal and recovery of Cr(VI) from tannery wastewater. The composite material was characterized via XRD, FTIR and SEM analyses. Under batch mode experiments, the composite achieved maximum adsorption of the Cr(VI) ion (99.53 ± 1.4%, i.e., 1636.49 mg of Cr(VI)/150 mg of adsorbent) at pH 2, adsorbent dose of 150 mg/10 mL of solution and 30 min of contact time. The adsorption process was endothermic, feasible and spontaneous and followed a pseudo-2nd order kinetic model. The Cr ions were completely desorbed (99.32 ± 2%) from the composite using 30 mL of NaOH solution (2M); hence, the composite exhibited high efficiency for five consecutive cycles without prominent loss in activity. The adsorbent was washed with distilled water and diluted HCl (0.1M), then dried under vacuum at 60 °C for reuse. The XRD analysis confirmed the synthesis and incorporation of magnetic iron oxide at 2θ of 30.38°, 35.5°, 43.22° and 57.36°, respectively, and graphene oxide (GO) at 25.5°. The FTIR analysids revealed that the composite retained the configurations of the individual components, whereas the SEM analysis indicated that the magnetic Fe₃O₄–NPs (MNPs) dispersed on the surface of the PMMA/rGO sheets. To anticipate the behavior of breakthrough, the Thomas and Yoon–Nelson models were applied to fixed-bed column data, which indicated good agreement with the experimental data. This study evaluates useful reference information for designing a cost-effective and easy-to-use adsorbent for the efficient removal of Cr(VI) from wastewater. Therefore, it can be envisioned as an alternative approach for a variety of unexplored industrial-level operations.     

Interferon α2–Thymosin α1 Fusion Protein (IFNα2–Tα1): A Genetically Engineered Fusion Protein with Enhanced Anticancer and Antiviral Effect

Human interferon α2 (IFNα2) and thymosin α1 (Tα1) are therapeutic proteins used for the treatment of viral infections and different types of cancer. Both IFNα2 and Tα1 show a synergic effect in their activities when used in combination. Furthermore, the therapeutic fusion proteins produced through the genetic fusion of two genes can exhibit several therapeutic functions in one molecule. In this study, we determined the anticancer and antiviral effect of human interferon α2–thymosin α1 fusion protein (IFNα2–Tα1) produced in our laboratory for the first time. The cytotoxic and genotoxic effect of IFNα2–Tα1 was evaluated in HepG2 and MDA-MB-231 cells. The in vitro assays confirmed that IFNα2–Tα1 inhibited the growth of cells more effectively than IFNα2 alone and showed an elevated genotoxic effect. The expression of proapoptotic genes was also significantly enhanced in IFNα2–Tα1-treated cells compared to IFNα2-treated cells. Furthermore, the HCV RNA level was significantly reduced in IFNα2–Tα1-treated HCV-infected Huh7 cells compared to IFNα2-treated cells. The quantitative PCR analysis showed that the expression of various genes, the products of which inhibit HCV replication, was significantly enhanced in IFNα2–Tα1-treated cells compared to IFNα2-treated cells. Our findings demonstrate that IFNα2–Tα1 is more effective than single IFNα2 as an anticancer and antiviral agent.     

Synthesis of Carbon Nanotubes (CNTs) from Poultry Litter for Removal of Chromium (Cr (VI)) from Wastewater

Pakistan, an agricultural country, raises 146.5 million commercial and domestic poultry birds, which generate around 544,831 tons of waste per year. This waste finds its final disposal in agricultural land as soil fertilizer or disposal site amendment. The usage of poultry litter for this purpose is uncontrolled, which results in environmental degradation such as emission of greenhouse gases, e.g., methane. However, alternative options such as thermochemical conversion of poultry litter can offer better solutions where this waste can be used as a low-cost carbon source for the synthesis of Multiwalled Carbon Nanotubes (MWCNTs). In this study, efforts were made to utilize this cheap and plentiful carbon source for the synthesis of CNTs in the presence of Ni/Mo/MgO as a catalyst, through pyrolysis. For a better yield of carbon product, the optimum ratio for the catalysts (Ni/Mo/MgO) was found to be 4:0.2:1. Furthermore, the process parameters were also optimized for better carbon yield. A good yield of CNTs resulted from a pyrolysis time of 12 min, a temperature of 825 °C, and a catalyst weight of 100 mg. The structure and morphology of the produced nanotubes were confirmed through X-ray Diffractometer (X-RD) and Scanning Electron Microscopy (SEM). The environmental application of the nanotubes was tested in a synthetic chromium solution in the lab using a batch experiment. Different experimental conditions (pH, adsorbent dosage, and contact time) were optimized to improve the adsorption of Cr (VI) by carbon nanotubes and a UV-Visible spectrophotometer was used at 540 nm to measure the absorbance of Cr (VI). The results showed that up to 81.83% of Cr (VI) removal was achieved by using 8 mg of CNTs at pH 3 with 400 rpm at 180 min of contact time. Thus, it was concluded that poultry litter can be a useful source for the synthesis of MWCNTs and thereby removal of Cr (VI) from industrial tanneries’ wastewater.     

Exploration of the Cs Trapping Phenomenon by Combining Graphene Oxide with α-K6P2W18O62 as Nanocomposite

A graphene oxide-based α-K₆P₂W₁₈O₆₂ (Dawson-type polyoxometalate) nanocomposite was formed by using two types of graphene oxide (GO) samples with different C/O compositions. Herein, based on the interaction of GO, polyoxometalates (POMs), and their nanocomposites with the Cs cation, quantitative data have been provided to explicate the morphology and Cs adsorption character. The morphology of the GO-POM nanocomposites was characterized by using TEM and SEM imaging. These results show that the POM particle successfully interacted above the surface of GO. The imaging also captured many small black spots on the surface of the nanocomposite after Cs adsorption. Furthermore, ICP-AES, the PXRD pattern, IR spectra, and Raman spectra all emphasized that the Cs adsorption occurred. The adsorption occurred by an aggregation process. Furthermore, the difference in the C/O ratio in each GO sample indicated that the ratio has significantly influenced the character of the GO-POM nanocomposite for the Cs adsorption. It was shown that the oxidized zone (sp²/sp³ hybrid carbon) of each nanocomposite sample was enlarged by forming the nanocomposite compared to the corresponding original GO sample. The Cs adsorption performance was also influenced after forming a composite. The present study also exhibited the fact that the sharp and intense diffractions in the PXRD were significantly reduced after the Cs adsorption. The result highlights that the interlayer distance was changed after Cs adsorption in all nanocomposite samples. This has a good correlation with the Raman spectra in which the second-order peaks changed after Cs adsorption.     

Oscillatory Mechanism of α-Fe(N) ↔ γ’-Fe4N Phase Transformations during Nanocrystalline Iron Nitriding

The kinetics of nanocrystalline α-iron nitriding to γ’-iron nitride in an ammonia atmosphere was studied at 598–648 K and at atmospheric pressure. Oscillatory changes in nitriding reaction rates depending on nitrogen concentration in a solid sample were observed. This phenomenon was explained by a gradual change in the iron active surface coverage degree, with nitrogen resulting from a gradual change in the free enthalpy of nitrogen segregation. The α-Fe(N) nanocrystallites’ transformation into γ’-Fe₄N went through six metastable FeN_x states. The continuous function proposed by Fowler and Guggenheim was modified to a stepwise variable function.     

The Application of Polycaprolactone Scaffolds with Poly(ε-caprolactone)–Poly(ethylene glycol)–Poly(ε-caprolactone) Loaded on Kidney Cell Culture

Human embryonic kidney cells are the host of adenovirus type-5 (Ad5) amplification. An Ad5-vector-based COVID-19 vaccine has been proven to be tolerated and immunogenic in healthy adults. Therefore, a rationally designed scaffold for culturing human embryonic kidney cells is useful for further studying its mechanism of action. Herein, a three-dimensional layered reticulated polycaprolactone (PCL) scaffold coated with poly(ε-caprolactone)-poly(ethylene glycol)-poly(ε-caprolactone) (PCEC) was developed to proliferate human embryonic kidney cells and to be used to amplify the Ad5 vector. The results indicate that PCEC improves the hydrophilicity and the cell culture ability of PCL cell culture scaffolds, resulting in a three times higher cell proliferation ratio of human embryonic kidney cells compared with those grown on bare PCL cell culture scaffolds. Meanwhile, the cytotoxicity test results showed that the scaffold material is noncytotoxic. This work provides an effective and scalable method for the in-depth study of adenoviruses.     

Influence of the Surface Chemistry of Graphene Oxide on the Structure–Property Relationship of Waterborne Poly(urethane urea) Adhesive

Small amounts—0.04 wt.%—graphene oxide derivatives with different surface chemistry (graphene oxide—GO-, amine-functionalized GO—A-GO-, reduced GO—r-GO) were added during prepolymer formation in the synthesis of waterborne poly(urethane urea) dispersions (PUDs). Covalent interactions between the surface groups on the graphene oxide derivatives and the end NCO groups of the prepolymer were created, these interactions differently altered the degree of micro-phase separation of the PUDs and their structure–properties relationships. The amine functional groups on the A-GO surface reacted preferentially with the prepolymer, producing new urea hard domains and higher percentage of soft segments than in the PUD without GO derivative. All GO derivatives were well dispersed into the PU matrix. The PUD without GO derivative showed the most noticeable shear thinning and the addition of the GO derivative reduced the extent of shear thinning differently depending on its functional chemistry. The free urethane groups were dominant in all PUs and the addition of the GO derivative increased the percentage of the associated by hydrogen bond urethane groups. As a consequence, the addition of GO derivative caused a lower degree of micro-phase separation. All PUs containing GO derivatives exhibited an additional thermal decomposition at 190–206 °C which was ascribed to the GO derivative-poly(urethane urea) interactions, the lowest temperature corresponded to PU+A-GO. The PUs exhibited two structural relaxations, their temperatures decreased by adding the GO derivative, and the values of the maximum of tan delta in PU+r-GO and PU+A-GO were significantly higher than in the rest. The addition of the GO derivative increased the elongation-at-break, imparted some toughening, and increased the adhesion of the PUD. The highest T-peel strength values corresponded to the joints made with PUD+GO and PUD+r-GO, and a rupture of the substrate was obtained.     

Thermal Stability and Dynamic Mechanical Properties of Poly(ε-caprolactone)/Chitosan Composite Membranes

Poly (ε-caprolactone) (PCL) and chitosan (CS) are widely used as biodegradable and biocompatible polymers with desirable properties for tissue engineering applications. Composite membranes (CS–PCL) with various blend ratios (CS:PCL, w/w) of 0:100, 5:95, 10:90, 15:85, 20:80, and 100:0 were successfully prepared by lyophilization. The thermal stabilities of the CS–PCL membranes were systematically characterized by thermogravimetric analysis (TG), dynamic thermogravimetry (DTG), and differential scanning calorimetry (DSC). It was shown that the blend ratio of PCL and CS had a significant effect on the thermal stability, hydrophilicity, and dynamic mechanical viscoelasticity of the CS–PCL membranes. All the samples in the experimental range exhibited high elasticity at low temperature and high viscosity at high temperatures by dynamic mechanical thermal analysis (DMTA). The performances of the CS–PCL membranes were at optimum levels when the blend ratio (w/w) was 10:90. The glass transition temperature of the CS–PCL membranes increased from 64.8 °C to 76.6 °C compared to that of the pure PCL, and the initial thermal decomposition temperature reached 86.7 °C. The crystallinity and porosity went up to 29.97% and 85.61%, respectively, while the tensile strength and elongation at the breakage were 20.036 MPa and 198.72%, respectively. Therefore, the 10:90 (w/w) blend ratio of CS/PCL is recommended to prepare CS–PCL membranes for tissue engineering applications.     

Vanadium (V) Adsorption from Aqueous Solutions Using Xerogel on the Basis of Silica and Iron Oxide Matrix

Vanadium is considered a strategic metal with wide applications in various industries due to its unique chemical and physical properties. On the basis of these considerations, the recovery of vanadium (V) is mandatory because of the lack of raw materials. Various methods are used to recover vanadium (V) from used aqueous solutions. This study develops a clean and effective process for the recovery of vanadium (V) by using the adsorption method. At the same time, this study synthesizes a material starting from silica matrices and iron oxides, which is used as an adsorbent material. To show the phase composition, the obtained material is characterized by X-ray diffraction showing that the material is present in the amorphous phase, with a crystal size of 20 nm. However, the morphological texture of the material is determined by the N₂ adsorption–desorption method, proving that the adsorbent material has a high surface area of 305 m²/g with a total pore volume of 1.55 cm³/g. To determine the efficiency of the SiO₂Fe_xO_y material for the recovery of vanadium through the adsorption process, the role of specific parameters, such as the L-to-V ratio, pH, contact time, temperature, and initial vanadium concentration, must be evaluated. The adsorption process mechanism was established through kinetic, thermodynamic, and equilibrium studies. In our case, the process is physical, endothermic, spontaneous, and takes place at the interface of SiO₂Fe_xO_y with V₂O₅. Following equilibrium studies, the maximum adsorption capacity of the SiO₂Fe_xO_y material was 58.8 mg (V)/g of material.     

Core-Shell Fe2O3@La1−xSrxFeO3−δ Material for Catalytic Oxidations: Coverage of Iron Oxide Core,Oxygen Storage Capacity and Reactivity of Surface Oxygens

A series of Fe₂O₃@LSF (La_0.8Sr_0.2FeO_3−δ perovskite) core-shell materials (CSM) was prepared by infiltration of LSF precursors gel containing various complexants and their mixtures to nanocrystalline aggregates of hematite followed by thermal treatment. The content of LSF phase and amount of carboxyl groups in complexant determine the percent coverage of iron oxide core with the LSF shell. The most conformal coating core-shell material was prepared with citric acid as the complexant, contained 60 wt% LSF with 98% core coverage. The morphology of the CSM was studied by HRTEM-EELS combined with SEM-FIB for particles cross-sections. The reactivity of surface oxygen species and their amounts were determined by H₂-TPR, TGA-DTG, the oxidation state of surface oxygen ions by XPS. It was found that at complete core coverage with perovskite shell, the distribution of surface oxygen species according to redox reactivity in CSM resemble pure LSF, but its lattice oxygen storage capacity is 2–2.5 times higher. At partial coverage, the distribution of surface oxygen species according to redox reactivity resembles that in iron oxide.     

Graphene Oxide@Heavy Metal Ions (GO@M) Complex Simulated Waste as an Efficient Adsorbent for Removal of Cationic Methylene Blue Dye from Contaminated Water

Graphene oxide (GO) was heavily used in the adsorption process of various heavy metal ions (such as copper (Cu) and iron (Fe) ions), resulting in a huge waste quantity of graphene oxide@metal ions complex. In this research, the authors try to solve this issue. Herein, the GO surface was loaded with divalent (Cu²⁺) and trivalent (Fe³⁺) heavy metal ions as a simulated waste of the heavy metal in various removal processes to form GO@Cu and (GO@Fe) composites, respectively. After that, the previous nanocomposites were used to remove cationic methylene blue (MB) dye. The prepared composites were characterized with a scanning electron microscope (SEM), transition electron microscope (TEM), Fourier transmission infrared (FTIR), Raman, and energy-dispersive X-ray (EDS) before and after the adsorption process. Various adsorption factors of the two composites towards MB-dye were investigated. Based on the adsorption isotherm information, the adsorption process of MB-dye is highly fitted with the Langmuir model with maximum capacities (mg g⁻¹) (384.62, GO@Cu) and (217.39, GO@Fe). According to the thermodynamic analysis, the adsorption reaction of MB-species over the GO@Cu is exothermic and, in the case of GO@Fe, is endothermic. Moreover, the two composites presented excellent selectivity of adsorption of the MB-dye from the MB/MO mixture     

The Role of the Graphene Oxide (GO) and Reduced Graphene Oxide (RGO) Intermediate Layer in CZTSSe Thin-Film Solar Cells

Cu₂ZnSn(S,Se)₄ (CZTSSe) solar cells with low cost and eco-friendly characteristics are attractive as future sources of electricity generation, but low conversion efficiency remains an issue. To improve conversion efficiency, a method of inserting intermediate layers between the CZTSSe absorber film and the Mo back contact is used to suppress the formation of MoSe₂ and decomposition of CZTSSe. Among the candidates for the intermediate layer, graphene oxide (GO) and reduced GO have excellent properties, including high-charge mobility and low processing cost. Depending on the type of GO, the solar cell parameters, such as fill factor (FF), were enhanced. Thus, the conversion efficiency of 6.3% was achieved using the chemically reduced GO intermediate layer with significantly improved FF.     

Fabrication and Adsorption Optimization of Novel Magnetic Core-shell Chitosan/Graphene Oxide/β-cyclodextrin Composite Materials for Bisphenols in Aqueous Solutions

A novel magnetic composite material, Fe₃O₄@SiO₂/chitosan/graphene oxide/β-cyclodextrin (MCGC), was prepared by multi-step methods. Various methods were used to systematically characterize the morphology, composition, structure, and magnetic properties of MCGC. The results obtained show that the composite material has good morphology and crystal structure and can be separated quickly by an external magnetic field. The operation is relatively easy, and the raw materials used to prepare this material are economical, easy to obtain, and environmentally friendly. The performance and adsorption mechanism for using this material as an adsorbent to remove bisphenol A (BPA) and bisphenol F (BPF) from water were studied. The adsorption parameters were optimized. Under optimal conditions, MCGC was found to remove more than 90% of BPA and BPF in a mixed solution (20 mg/L, 50 mL); the adsorption process for BPA and BPF on MCGC was found to follow a Redlich–Peterson isotherm model and Pseudo-second-order kinetic model. The adsorption mechanism for MCGC may involve a combination of various forces. Recycling experiments showed that after five uses, MCGC retained a more than 80% removal effect for BPA and BPF, and through real sample verification, MCGC can be used for wastewater treatment. Therefore, MCGC is economical, environmentally friendly, and easy to separate and collect, and has suitable stability and broad application prospects.