Adsorption Of Anions Research Articles

Inglet oxygen generaion via silver nanoparticles UV-photoexcitation

The NIR-luminescence of suspension of silver nanoparticles stabilized in distilled water has been investigated by photoexcitation of surface plasmon resonance (SPR). The observed short-living luminescence with the spectral maximum at 1300 nm is attributed to the singlet oxugen molecules luminescence. The singlet oxygen generation is assumed to pass in two stages as a result of three-photon process. First the one-photon SPR excitation of silver nanoparticle is occurred and leads to superoxide oxygen generation on the nanoparticle surface. Next the superoxide anion absorbs two more photons of the same laser pulse resulting in electron photodetachment with singlet oxygen formation. During a long period of UV-irradiation the studying suspension ceases to be photostable and sedimentation occurs. The sedimentation may be related to disturbance of nanoparticles steric stability resulting in more efficient superoxide anion adsorption on nanoparticles surface with silver oxide formation.

Understanding the Role of Calcium Lignosulphonate in Flotation Separation of Chalcopyrite from Talc

ABSTRACT Talc is a naturally hydrophobic mineral. Its separation from sulfide minerals is a tough issue in froth flotation. In this study, calcium lignosulphonate (CLS) was introduced as a talc depressant during sodium isobutyl xanthate (SIBX) flotation of chalcopyrite. The micro-flotation findings showed that under pH 5.0–10.5, the combination application of CLS and SIBX achieved a selective flotation separation of chalcopyrite from talc. The results of zeta potential, contact angle, adsorption capacity and in-situ AFM deduced that both talc and chalcopyrite exhibited a favorable affinity toward CLS, and SIBX hardly changed the adsorption of CLS on talc surface, while significantly reduced that on chalcopyrite. The Ca2+ ions of CLS played a bridging role in connecting lignosulphonate (LS) anions and the negatively charged Si-O layers through electrostatic attraction, which transformed talc surface from hydrophobicity into hydrophilicity. The Cl− ions weakened the adsorption of LS anions on the Ca2+-modified talc surface, and the adsorption affinity of Na+ ion toward the Si-O layers was much weaker than that of Ca2+ ion. Thus, CLS exhibited the strongest depression against talc’s floatability, followed by CaCl2 + SLS (sodium lignosulphonate), and then SLS. SIBX chemisorbed on to chalcopyrite via forming the surface Cu-IBX complexes, which removed the adsorbed LS anions and recovered the floatability of chalcopyrite. The CLS-hydrophilized talc and SIBX-hydrophobized chalcopyrite exhibited the different surface wettability, and they both loaded negative charges, which prevented the aggregation of their particles, resulting in a highly efficient flotation separation chalcopyrite from talc.

Enhancing understanding of anionic surfactant adsorption mechanism and hydrophilic modification of bituminous coal for effective dust suppression

The large amount of coal dust generated by mechanized coal mining poses hazards such as coal mine explosions, coal worker pneumoconiosis, and atmospheric pollution. Spray dust suppression is widely employed as a coal dust control technology in the mining process, with anionic surfactants commonly used as highly effective wetting and enhancing agents. However, the application process lacks theoretical guidance on the interaction mechanism between anionic surfactants and coal dust. This study aims to investigate the adsorption mechanism between anionic surfactants and coal dust surfaces, focusing on two specific surfactants: sodium dioctyl sulfosuccinate (AOT) and sodium dodecyl sulfate (SDS). Both surfactants possess the same hydrophilic group but differ in their tail chain groups. Through a comprehensive analysis, this research provides insights into the essential properties and characteristics of AOT and SDS adsorption on bituminous coal. Static adsorption experiments revealed that AOT exhibited a higher maximum adsorption capacity (Qe) on coal dust compared to SDS. Scanning electron microscopy and particle size characterization analysis demonstrated AOT's notable tendency to cluster coal dust particles. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy investigations confirmed a significant hydrophilic modification induced by AOT on the coal dust surface. Quantum chemistry calculations revealed that Van der Waals adsorption played a fundamental role in the interaction between the AOT and SDS tail chains and the coal surface. The double tail chain structure of AOT contributed to a more stable and stronger adsorption configuration with coal molecules. These findings provide valuable theoretical insights for the development and application of effective dust suppressants.

Cationic cellulose nanofibers/chitosan auxiliary-dominated win-win strategy for paper yarn with superior color and physical performances

The colored and high-saline effluents during the traditional dyeing process poses serious environmental challenge. In our study, an eco-friendly cationic cellulose nano-fiber/chitosan (CCNF/CS) binary versatile auxiliary was designed for the neutral salt-free dyeing and physical enhancement of paper by mixing with pulp simply. Profiting from the rich cationic binding sites of CCNF/CS (Charge density: 3749.67 μmol/g), under near neutral conditions (pH = 6.2), the maximum adsorption capacity of anionic GL (Direct fast turquoise blue GL) on paper with 0.5 % CCNF/CS reached 1865.06 mg/g with a desirable evenness (45.5 % and 92.1 % higher than that of CCNF and NaCl group, respectively), and the dye uptake was up to 97 %. The spontaneous adsorption behavior was aligned with the pseudo-second-order and Langmuir models, with a primary physical mechanism enhanced by chemical forces. The combination of strong electronic attraction, hydrogen bonding, and n-π stacking effects granted CCNF/CS an enhanced proficiency in anionic dye adsorption. In addition, the tensile strength of the resulting paper yarn with 0.5 % CCNF/CS increased to 52.47 MPa under the optimal parameters, deriving from the CCNF/CS-induced inter-fiber cohesion. Overall, our research provided a green promising approach for the innovative neutral salt-free dyeing and mechanical enhancement of paper.

Potassium-Bicarbonate-Induced Mineralized Acid Mine Drainage into Iron Hydroxyl Sulfate Minerals for Better Water Remediation and Resource Reuse

Iron hydroxyl sulfate minerals (IHSMs, including schwertmannite and jarosite) are a promising material for environmental applications with excellent adsorption of metal oxygen anions. The acid mine drainage (AMD) abundant in iron and sulfate ions holds potential for the production of valuable IHSMs, thereby achieving resource recycling whilst simultaneously mitigating water contamination, which is important for the sustainable remediation of AMD. Conventional mineralization, which promotes the generation of minerals from Fe3+ and SO42− through the energy provided by chemical or biological oxidation, can only partially mineralize iron in AMD containing substantial quantities of Fe2+. In this study, an improved method for mineralizing AMD containing iron of a different valence into IHSMs under the induction of KHCO3 was proposed. For AMD containing Fe2+, the combination of KHCO3 and H2O2 was used to promote the hydrolysis of iron (92.7%) and sulfate (11.1%) into IHK minerals, which resulted in a significant increase in iron removal of 75.2% and a minor increase in sulfate removal of 4.9%, compared with the formation of schwertmannite from oxidation solely involving H2O2. For the AMD containing Fe3+, the energy generated by the acid–base reaction in water could also directly promote the formation of IK minerals from 97.2% iron and 6.9% sulfate. XRD and FTIR analyses confirmed the identification of the IHK and IK minerals as IHSMs transitioning from schwertmannite to jarosite. SEM and elemental analyses indicated that the mineral exhibited denser aggregate spheres with the incorporation of KHCO3 in mineralization yet displayed enhanced mineralization abilities for the contaminant ions in AMD. Moreover, despite the SSA of the modified minerals being diminished (2.02, 1.83 and 1.83 m2/g for IH, IHK and IK, respectively), the presence of more sulfate in the mineral enhanced the adsorption capacity of Cr(VI). Furthermore, the water quality results also illustrated that the removal ratios of iron and sulfate in AMD notably increased with the involvement of KHCO3 in mineralization. In conclusion, the KHCO3-induced mineralization of iron-containing (either divalent or trivalent) AMD into IHSMs not only improved the mineralization ratios and contaminant removal ratios for better remediation of AMD but also obtained mineral resources with better adsorption of Cr(VI), thereby fostering the sustainable advancement of the remediation of AMD. Therefore, this innovative strategy employing KHCO3-assisted chemical mineralization to form IHSMs holds ample potential and promises to be an efficacious methodology for the sustainable remediation of iron-rich AMD.

Arsenate Anion-π Interactions on Amine-Modified Polydivinylbenzene in Aqueous Systems: Experimental and Theoretical Investigation.

Anion-π interactions aiding in the adsorption of anions in the solution phase, though challenging to quantify, have attracted a lot of attention in supramolecular chemistry. We present the design of a polymer adsorbent that quantifies the adsorption of arsenate ions experimentally by optimizing anion-π interactions in a purely aqueous system and use density functional theory to compare these results with theoretical data. Arsenate anions are removed from water by amine-functionalized polydivinylbenzene using the comonomer 1-vinyl-1,2,4-triazole, which was cross-linked with divinylbenzene via radical polymerization in a hydrothermal procedure. The amine-functionalized polydivinylbenzene successfully removed arsenate anions from water with a capacity of 46 mg g-1, a 70% increase compared to the nonfunctionalized polydivinylbenzene (27 mg g-1) capacity under the same conditions. Adsorption is best described by the Sips isotherm model with a correlation coefficient R2 factor of 0.99, indicating that adsorption sites are homogeneous, and adsorption occurred by forming a monolayer. Kinetic studies indicated that adsorption is second order in the amine-functionalized polydivinylbenzene. Computational studies using density functional theory showed that the 1-vinyl-1,2,4-triazole comonomer improved the thermodynamic stability of the anionic-π interactions of polydivinylbenzene with arsenate anions. Electrostatic interactions dominate the mechanism of adsorption in polydivinylbenzene compared to the anion-induced interactions that dominate adsorption in amine-functionalized polydivinylbenzene.

Overview - Developing and Modifying Ettringite and Iron-Ettringite for Enhanced Adsorption of Anions and Cations Pollutants

Overview - Developing and Modifying Ettringite and Iron-Ettringite for Enhanced Adsorption of Anions and Cations Pollutants

Functionalized Magnesium Phosphate Cement Induces In Situ Vascularized Bone Regeneration via Surface Lyophilization of Chondroitin Sulfate.

Bone defect repair poses significant challenges in orthopedics, thereby increasing the demand for bone substitutes. Magnesium phosphate cements (MPCs) are widely used for bone defect repair because of their excellent mechanical properties and biodegradability. However, high crystallinity and uncontrolled magnesium ion (Mg2+) release limit the surface bioactivity of MPCs in bone regeneration. Here, we fabricate chondroitin sulfate (CS) as a surface coating via the lyophilization method, namely CMPC. We find that the CS coating is uniformly distributed and improves the mechanical properties of MPC through anionic electrostatic adsorption, while mediating degradation-related controlled ion release of Mg2+. Using a combination of in vitro and in vivo analyses, we show that the CS coating maintained cytocompatibility while increasing the cell adhesion area of MC3T3-E1s. Furthermore, we display accelerated osteogenesis and angiogenesis of CMPC, which are related to appropriate ion concentration of Mg2+. Our findings reveal that the preparation of a lyophilized CS coating is an effective method to promote surface bioactivity and mediate Mg2+ concentration dependent osteogenesis and angiogenesis, which have great potential in bone regeneration.

Atomic arrangement analysis and crystal growth mechanism of HAp nanocrystal synthesized from amorphous calcium phosphate

AbstractThe crystal growth of hydroxyapatite (HAp) using a solvothermal method was investigated under various reaction conditions. The purpose of the present study is the synthesis of HAp nanocrystals with multiple facets and the atomic arrangement for various orientations of the crystal was clarified. HAp nanorods were obtained at 200°C after 24 h using a reaction medium of water. The atomic arrangement in HAp nanorods was examined for a characteristic facet in the direction of [21−13−] and [0110−] incidences and crystal orientation along the c‐axis of HAp nanorod was confirmed using electron microscopy. The present study clarifies the HAp crystal growth mechanism, where the adsorption of cations or anions onto the crystal facet determines the HAp crystal shape. The crystals of HAp grew along the c‐axis and became rod‐shaped suggesting that cations were adsorbed predominantly over anions.

The role of surface chemistry in the synthesis of supported CuPd bimetallic/intermetallic catalysts for selective hydrogenation reactions

Understanding and controlling the structure of supported bimetallic/intermetallic catalysts are crucial for many heterogeneous catalytic reactions. However, commonly used synthesis techniques such as coimpregnation and coadsorption often yield nonuniform alloying and phase segregation, largely owing to the lack of interactions between different metal precursors. Here we show that by adopting sequential adsorption of complex metal cations and anions with the assistance of a proper ligand, the interaction between different metal precursors is enhanced, thus resulting in uniformly alloyed intermetallic catalysts. The supported CuPd intermetallic catalyst exhibits greatly improved selectivity towards monoolefins in the semihydrogenation of acetylene and butadiene compared to those random CuPd alloys synthesized via coimpregnation and coadsorption methods.

Chitosan and silica nanoparticles-modified xanthan gum-derived bio-nanocomposite hydrogel film for efficient uptake of methyl orange acidic dye

In this contribution, a bio-nanocomposite hydrogel film (CS/XG.SiO2) of chitosan/silica NPs-modified xanthan gum was prepared via a facile solution casting blending approach and utilized to capture the anionic methyl orange (MO) from aqueous solution. A Taguchi standard method was used to optimize the hydrogel nanocomposite synthesis reaction conditions after comprehensive characterization using various techniques. Under various operating parameters, the hydrogel biofilm was tested for its effectiveness in adsorbing MO dye in a batch process. In agreement with Langmuir isotherm, the CS/XG.SiO2 biofilm was capable of adsorbing MO at a maximum capacity of 294 mg/g at pH 5.30, contact time 45 min, temperature 25 °C, and concentration (C0) 50 mg/L. Pseudo-second-order model and adsorption kinetics data well matched. The thermodynamic data indicate that adsorption occurred spontaneously and exothermically. The main mechanisms driving the adsorption are electrostatic interactions and hydrogen bonding between the CS/XG.SiO2 nanocomposite and the dye. Furthermore, the biofilm is regenerative, allowing for up to five reuses while maintaining a 75 % dye removal efficiency. This study highlights that the CS/XG.SiO2 hydrogel nanocomposite is an inexpensive, reusable, and eco-friendly bio-adsorbent that is capable of anionic dye adsorption.

Effect of Electrolyte Anions on the Activity of Iridium Oxide Catalysts for Water Electrolysis

Developing environmentally friendly and renewable energy sources is essential due to the environmental and energy security issues caused by traditional combustion of fossil fuel-based energy sources. Therefore, as a clean and sustainable energy carrier, hydrogen has attracted great attention in recent years. In this regard, water electrolysis utilizing renewable energy sources to produce hydrogen is considered one of the most promising technologies. It is believed elucidation of the reaction mechanism of highly active iridium oxides is promising for the further development of cost-efficient PEM water electrolysis catalysts. The properties of the MEA could be affected by many parameters such as the catalysts, operating temperature, and pressure1,2. Another important factor is the cation impurities that can be found in the circulating water, which could severely degrade the MEA performance during the operation of a PEM water electrolyze. However, there are less reports on anion impurities such as SO4 2- and PO4 3-. Therefore, in this study, the relationship between electrolyte anions and OER activity was investigated for IrOx catalysts with different crystal structure. By using operando X-ray absorption spectroscopy (XAS), we investigated the electronic state of Ir and O under operation potential.IrOx with different degree of crystallinity (SA3.5 and SA58) were provided by Tanaka Kikinzoku Kogyo K.K., Chemical & Refining Company and named after their BET surface areas. These two samples were then tested for electrochemical properties in different concentrations of phosphoric acid and perchloric acid, respectively. The electrochemical measurements were performed using a standard three-electrode cell connected to an MPG-205-NUC system (Bio-Logic). The cyclic voltammograms (CV) were scanned from 0.1 V to 1.2 V vs. RHE at 50 mV s-1. The electrochemical activities of the catalysts were subsequently investigated using linear sweep voltammetry (LSV) in the range of 1.1 to 1.7 V vs RHE at 10 mV s−1. operando XAS were collected using a home-made flow-type cell, where Pt wire and RHE worked as counter and reference electrodes, respectively. The catalyst ink was coated onto an Nafion membrane to prepare both the X-ray window and working electrode. The electrolyte was circulated at the flow rate of 100 mL min-1.The catalytic performance of IrOx was investigated at different types and content of electrolyte under H3PO4 and HClO4. Figure 1 shows the CVs of SA3.5 and SA58 under different types and content of electrolyte. In the presence of phosphate anions, SA3.5 showed a tendency to decrease Ir redox between 0.6 and 1.1 V with increasing electrolyte concentration. On the other hand, there were no obvious changes in SA58. It was found that IrOx catalysts have an great effect of specific adsorption of anions and low symmetry of monoclinic phase catalysts (SA 3.5) are more susceptible to anion poisoning. Figure 2 shows the result of examining the poisoning mechanism using soft X-ray XAS. O K-edge results present the formation of µ2-O (O-O) bond at around 528.7 eV, which was previously observed by Nong, H. N. et. al. through operando O-K edge measurements during OER process3. The peak intensity at 528.7 eV of the amorphous samples was in the same order as the OER activities. According to potential dependence change of the pre-edge peak, under the presence of phosphate anions, the hole formation to Ir-O hybrid orbitals was suppressed in SA3.5. This result indicates that the anion adsorbs to the active site, poisoning the catalyst surface and inhibiting the reaction. Acknowledgements This work is based on results obtained from a project (JPNP14021) commissioned by the New Energy and Industrial Technology Development Organization (NEDO) of Japan. References Zhang, Y.; Zhu, X.; Zhang, G.; Shi, P.; Wang, A.-L.; et al. J. Mater. Chem. A: 2021, 9, 5890-5914.Chen, Z.; Duan, X.; Wei, W.; Wang, S.; Ni, B.-J.; et al. Nano Energy: 2020, 78, 105270.Nong, H. N.; Falling, L. J.; Bergmann, A.; et al. Nature 2020, 587 (7834), 408-413. Figure 1

Effect of Chlorine on Copper Electrodissolution

A computational study on the role of adsorbed Cl ions on copper dissolution is presented. Extensive grand canonical Monte Carlo (GCMC) calculations using reactive force-field (ReaxFF) are used to check the formation chlorine (Cl) adlayer structures on Cu (100) surface as a function of the chemical potential (µ). From experimental studies conducted by other researchers it has been observed that Cl adlattice on Cu in c(2X2) at maximum coverage. We observe that at low µ, Cl adlayer is disordered and moves to ordered c(2X2) structure at high µ. The binding energy of Cl, oxygen (O), hydroxide (OH-) and H2O on Cu at different sites is calculated and compared with Density-functional theory (DFT) values. Metal surface is often highly uneven and rough during electrodissolution process. Therefore, we also discuss the adsorption isotherm, disorder-order transformation, and preferential adsorption sites for rough surfaces. Specific anion adsorption (SAA) of Cl involves partial charge transfer to Cu substrate and these effect the type of bond and bond strength which is also briefly discussed. The electrodissolution of Cu in the presence of Cl is modelled using kinetic Monte Carlo simulation to obtain the polarization curve.Keywords: Adsorbed chlorine, electrodissolution, grand canonical monte carlo, molecular dynamics, ReaxFF, kinetic monte carlo.

Removal of cationic dyes from aqueous solution using polyacrylic acid modified hemp stem.

Water pollution caused by dyes is a pressing environmental challenge due to their persistence and difficulty in degradation. Herein, an anionic adsorbent (HS-PAANa) was synthesized by grafting polyacrylic acid (PAA) onto the agricultural waste-hemp stem (HS). The obtained HS-PAANa adsorbent exhibited rapid adsorption kinetics, high adsorption capacity, and a favorable preference for cationic dyes, such as methylene blue (MB) and crystal violet (CV). The experimental data fit well with the pseudo-second-order kinetic model and Langmuir isotherm, demonstrating the efficiency of HS-PAANa in dye removal. Notably, the optimal adsorption capacities of HS-PAANa for MB and CV were found to be 1296.65 mg/g and 1451.43 mg/g, respectively. In the cationic/anionic dyes (MB/MO) binary systems, HS-PAANa exhibited enhanced selective adsorption of cationic dyes (MB), indicating its potential for targeted removal of specific dyes from mixed solutions. Moreover, HS-PAANa adsorption shows an excellent recyclability, after five cycles, HS-PAANa still maintained MB and CV removal rates of 93.85% and 95.08%, respectively. Therefore, the bioadsorbent HS-PAANa exhibits high potential as a highly efficient adsorbent for the effective treatment of cationic pollutants in wastewater.

Rational design of self-assembled copper oxide nanoparticles into hierarchical nanorods with high-surface-area for environmental remediation of wastewater

The coordinated generation of hierarchical structures is a difficult task that necessitates accurate control over a number of variables such as assembly shape, array dimensions, peripheral spacing, and uniformity. In this study, we successfully synthesized self-assembled copper oxide nanomaterials using hydrothermal processes. By aggregating copper oxide nanoparticles (diameter 4–6 nm), we were able to create a hierarchical rod-like morphology with highly homogeneous particle morphology and feature sizes ranging from 50 to 200 nm. We thoroughly investigated the methods of self-assembly of CuO nanorod formations, as well as the influence of templates on the materials' structure. Our analysis included powder X-ray diffraction (XRD), TEM, N2 sorption, and X-ray photoelectron spectroscopic (XPS) methods. N2 adsorption–desorption isotherm indicated high surface areas (125–190 m2/g) and limited pore diameter (less than 5 nm) for different samples. Furthermore, XPS examination demonstrated that the materials have a high concentration of Cu2+ groups, which serve as active sites for dichromate anion adsorption. We further investigated the adsorption process using Langmuir, Freundlich and Weber–Morris models and found that these CuO nanorods can perform as a highly powerful and recyclable adsorbent for hazardous dichromate from wastewater. Our findings have significant implications for the progress of new materials for environmental remediation and other applications.

Porous NiCo-LDH microspheres obtained by freeze-drying for efficient dye and Cr(VI) adsorption

Hierarchical NiCo-LDH microspheres (NiCo-LDHM) were synthesized via a simple one-step hydrothermal process in the presence of 2-methylimidazole, and a freeze-drying technique was subsequently used to further adjust its microstructure. The obtained porous hierarchical microspheres are about 5 µm in average diameter, and consist of ultrathin nanosheets with an average thickness of 5 nm. The freeze-drying endows LDH microspheres with higher surface area and improved pore structure. The unique hierarchical porous structure, high specific surface area and positive surface charge together contribute NiCo-LDHM’ excellent capability for anionic dyes and heavy metal ions removal, its theoretical adsorption capacities for Congo red (CR), acid fuchsin (AF) and Cr(VI) are 2120, 1176 and 123 mg/g at room temperature respectively. The adsorption of pollutant molecules/ions onto NiCo-LDH microspheres conforms to the quasi-secondary kinetics model. Isotherm studies suggest that the CR adsorption onto adsorbent fits Langmiur model, while AF/Cr(VI) adsorption fits Freundlich model, indicating that the size and morphology of pollutant molecules influence the adsorption process. The adsorption is a spontaneous endothermic process and NiCo-LDHM demonstrates good recyclability, the removal rates of CR, AF and Cr(VI) can still reach 90.7%, 84.7% and 82% after five cycles, respectively. In addition, NiCo-LDH hierarchical microspheres also exhibit good anionic selective adsorption capacity in mixed-dye systems, displaying great potential for water restoration and dye recycling.

Cationic and anionic dyes adsorption from wastewater by clay-chitosan composite: An integrated experimental and modeling study

Water contamination with organic dyes is a significant environmental concern because it results in serious problems that threaten public health. In this study, a clay-based composite from Safi City, coated with chitosan (Cs), was used as an adsorbent (SRC/Cs) to remove co-existing dyes (methylene blue (MB) and congo red (CR)) from aqueous solution. Characterization methods such as Fourier infrared transform spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) coupled with EDX, and zero charge point determination were performed to understand the adsorption mechanisms of the co-pollutants in the adsorbent’s surface. The effects of pertinent parameters, such as initial dye concentration, adsorbent's dose, reaction time, pH, and temperature, were optimized to maximize the adsorption of both anionic and cationic dyes. The Langmuir, Freundlich, and Temkin isotherm models were applied to simulate experimental data. The DFT method was used to identify the key mechanism for MB and CR adsorption. It was found that the composite with 30% (w/w) CS and 70% (w/w) clay showed a complete removal of the target dye with an initial dye concentration of 20 mg/L at optimized pH 2 (CR) and pH 4 (MB), 60 min of reaction time, and 600 rpm of agitation speed. The Langmuir model was suitable for modeling the MB dye adsorption, while the Temkin isotherm was representative to describe CR adsorption. The adsorption capacities of both MB and CR dyes were 97.08 mg/g and 80.9 mg/g, respectively. The kinetic study showed that their adsorption process followed the pseudo-second-order. Thermodynamic parameters such as ΔH0, ΔG0, and ΔS0 imply that the adsorption reaction was spontaneous and endothermic. Overall, this study implies the potential of the composite as a novel adsorbent for removing MB and CR in single and binary systems.

Regulating the Electrical Double Layer with Supramolecular Cyclodextrin Anions for Dendrite-Free Zinc Electrodeposition.

The interfacial stability of a Zn battery is dependent on the electrical double layer (EDL) that forms at the interface between the electrolyte and the Zn metal anode. A fundamental understanding of the regulation of the EDL structure and stability on the Zn surface is highly desirable for practical applications of aqueous batteries. Herein, the interfacial chemistry of the EDL is regulated by the adsorption of supramolecular cyclodextrin anions in the inner Helmholtz plane (IHP). The nucleation overpotential and the charge transfer activation energy for Zn2+ to go through the OHP (Ea1) and IHP (Ea2) are increased, leading to slower Zn2+ transfer kinetics. The electric field distribution and Zn2+ flux in the proximity of the Zn metal surface are homogenized, thus suppressing the growth of dendrites. The mechanism is supported with theoretical and experimental analyses. Consequently, a Zn||Zn symmetric cell achieves an ultrahigh cumulative capacity of 10000 and 4250 mAh cm-2 at a respective current density of 10 and 50 mA cm-2, and an average Coulombic efficiency of 99.5% over 1000 cycles under harsh conditions (at a high current density of 10 mA cm-2 with a high capacity of 10 mAh cm-2). This work provides insight into the introduction of supramolecular anions to regulate the electrical double layer EDL structure and improve the interfacial stability.

Development of environmentally-friendly modified bioadsorbents for water treatment

As a result of scientific research, it was found that synthesized pure sorbents based on a composite of Fe3O4 nanoparticles and AlgBT have an increased adsorption capacity due to the inclusion of double hydroxides and an alginate matrix. The processes of complex formation occur according to the principle of maximum inheritance of the structural features of the original coordination compounds, which make it possible to predict and implement the hypothetical structures of new compounds. All this significantly improves the adsorption capacity of the developed adsorbents with respect to phosphate ions. Modified sorbents with a clay basis are therefore a particularly intriguing field. The current research constructed and described modified sorbents, and then conducted tests in the laboratory to determine how well they absorbed phosphate. This study used spectroscopic techniques (SEM, FTIR, X-ray diffraction, and XRD analytical methods) to examine the structure and physicochemical characteristics of improved ecologically friendly sorbents based on alginates, bentonite, and nanoparticles. The alginate core may be physically and chemically modified and can take part in a variety of phosphate anion adsorption methods thanks to the active COOH and OH groups that are present there. The sorption efficiency was established for a modified Fe3O4NPs@AlgBT. Equilibrium in the system sorbent-an aqueous solution of Na2HPO4 is established in 10 hours after the start of sorption, while two-thirds of all sobbed anions pass into the solid phase during the first two hours. The limiting sorption of phosphate ions on modified Fe3O4NPs@AlgBT reaches 410 mg/g, which makes it possible to offer it as an effective sorbent for industrial wastewater treatment

Toward pulping process for enhancing the RS-black liquors as precursor of activated carbons for aqueous adsorbent purposes

This work deals with providing a green pulping process of rice straw with zero waste discharged, via valorization of its by-product as a promising precursor for production of carbon nanostructures. The carbon nanostructures (BL-CNSs) from rice straw pulping liquors (BLs) are prepared in one step with phosphoric acid activation. The carbon nanostructures (BL-CNSs) from rice straw pulping liquors (BLs) are prepared in one step with phosphoric acid activation. The optimal pulping approach for achieving effective adsorbent (BL-CNSs) of cationic and anionic dyes is recommended from using different BLs precursors resulting from different reagents (alkaline, neutral, and acidic reagents). The carbon precursors are characterized by elemental, thermal (TGA and DTG) and ATR FTIR analyses. While the impact of pulping route on performance of CNSs is evaluated by their adsorption of iodine, cationic dye and anionic dye, as well as ATR-FTIR, textural characterization, and SEM. The data of elemental analysis displayed a high Carbon content ranges from 57.85 to 66.69% suitable for CNSs preparation, while the TGA showed that Sulphur-containing BLs (Kraft, neutral sulfite and acidic sulfite) have higher degradation temperature and activation energies as compared with other BLs. The optimum BL-CNSs adsorbent is prepared from the disposed neutral sulfite black liquor, with the following characteristics: cationic dye adsorption capacity 163.9 mg/g, iodine value 336.9 mg/g and SBET 310.6 m2/g. While the Kraft-CNSs provided highest anionic adsorption (70.52 mg/g). The studies of equilibrium and kinetic adsorption of dyes showed that the adsorption equilibrium of all investigated BL-CNSs toward MB follow the Langmuir and mainly Freundlich models for BB adoption. Their adsorption kinetics are a good fit with the pseudo-second-order model. The textural characterization and SEM revealed the CNSs exhibit a mixture of mesoporous and microporous structure.