Saturated Adsorption Research Articles

Efficient adsorption and rapid electrochemical degradation of methyl methacrylate (MMA) by three-dimensional nanostructured carbon anode

Methyl methacrylate (MMA) is a widely used oxygen-containing volatile organic compound, functioning as both an organic solvent and additive. Therefore, the advancement of effective methods for MMA removal is of great significance. In this study, three-dimensional nanostructured carbon (CNTs/CC) anode materials were prepared through the in-situ growth of carbon nanotubes (CNTs) on carbon cloth (CC) using chemical vapor deposition (CVD). The prepared material showed outstanding adsorption-electrocatalytic degradation performance towards MMA, with a saturated adsorption capacity of 2033 mg·g−1 and complete degradation achieved after 90 min of electrification at a 100 mg·L−1 MMA concentration. The electrochemically active surface area increased to 29.8 cm2 with an Rs value of 2.35 Ω for the CNTs/CC-2 anode material, leading to enhanced ·OH generation capability and faster degradation rates. The material also exhibited excellent reusability over thirteen cycles of adsorption-electrochemical degradation of MMA, with a degradation efficiency consistently above 92 %. This research provides valuable insights for developing new materials and technologies for MMA degradation.

Activated Carbon Based on Recycled Epoxy Boards and Their Adsorption toward Methyl Orange.

With the swift progress of the electronics industry, discarded circuit boards have become an important source of non-degradable waste. In this work, discarded epoxy resin was collected as a precursor to prepare activated carbon (AC) through stepwise carbonization/activation methods. The rough carbon materials with a certain graphite and amorphous structure reveal the multiple oxygen-containing groups on their surface. In the process of studying the adsorption of methyl orange by activated carbon, it is found that the adsorption is in accordance with the quasi-secondary kinetic model, and equilibrium adsorption amounts can reach 41.051 mg/g. The adsorption isotherm of AC is more in line with the Langmuir model, and the saturation adsorption amount at three different temperatures is 23.137 mg/g, 30.358 mg/g, and 37.202 mg/g, respectively. The enthalpy (ΔH) is 17.30 KJ/mol in the adsorption process, which indicates that is a physical process with heat-absorbing capabilities. This work is of great significance with regard to the recycling of waste to reduce pollution and in terms of gaining economic benefits.

Effect analysis of temperature and initial water content on the adsorption and separation of VOCs by ZIF‐8 based on molecular simulation

AbstractVolatile organic compounds (VOCs) have seriously polluted the atmospheric environment and caused harmful effects on human beings, so it is imperative to control oil vapor emissions. Metal organic framework materials, as one of the porous materials, have a good application prospect in the field of gas adsorption separation. In this paper, the effects of temperature and initial water content (IWC) on the adsorption properties of methane (CH4), ethane (C2H6), ethylene (C2H4), propane (C3H8), and propylene (C3H6) by ZIF‐8 were studied by combining the large gauge Monte Carlo (GCMC) and ideal adsorption solution theory. The results show that the higher the temperature is, the lower the adsorption capacity is, the higher the threshold pressure is, and the single molecule interaction energy changes little with temperature. But pore volume is still the main influencing factor. The IWC also reduces the saturated adsorption capacity. Preloaded water molecules can enhance the electrostatic interaction at low pressure, thus affecting the adsorption heat and interaction energy of single molecules. Overall, these findings provide valuable mechanistic insights into the effects of temperature and IWC on the adsorption properties of ZIF‐8 for VOCs.

DISPERSION OF AQUEOUS Y2O3 NANO-SUSPENSION AND FABRICATION OF TRANSPARENT CERAMICS BY COLLOIDAL PROCESSING

In the present study, transparent Y2O3 ceramics were successfully fabricated via colloidal processing, employing polyethylenimine (PEI) as an effective dispersant. The effect of PEI on nanosized Y2O3 suspensions was characterized by zeta-potential, adsorption behavior, rheological properties, and sedimentation test. The addition of PEI shifted the IEP of the Y2O3 powder towards a more alkaline pH range, and the adsorption of PEI on the Y2O3 surfaces gradually increased with the amount of PEI until reaching the saturation adsorption at 1.5 w/%. The PEI amount of 1.5 w/% was superior for the preparation of Y2O3 suspension as a result of a lower viscosity or sedimentation behavior. The viscosity of the suspension depended on the solids loading, increasing with the amount of powder. The optimal rheological behavior was achieved with 29 /% Y2O3 in the suspension, enabling the centrifugal slip casting of complex-shaped green bodies with a packing density of 43 %. Including an additional CIP treatment boosted the packing density of the green compacts, achieving above 50 %. Vacuum sintering the compacts at 1700 °C for 5 h yielded high-density ceramics exhibiting an in-line transmittance of approximately 73 % at a wavelength of 1100 nm.

Simultaneous super-stable mineralization of Pb2+, Cd2+ and Cu2+ using MIL-101(Fe)@MgFe-LDH

The Pb2+, Cd2+ and Cu2+ co-existing pollution in battery and smelting industries have posed a significant threat to ecosystem and human health. Herein, we reported the fabrication of MIL-101(Fe)@MgFe-LDH successfully using in-situ nucleation and transformation strategy. The MIL-101(Fe)@MgFe-LDH exhibited maximum saturated adsorption capacities of 1408.57, 568.18 and 366.30 mg g−1 towards Pb2+, Cd2+ and Cu2+ in aqueous solution, respectively, and the adsorption data for each of these heavy metals can be well-fitted with pseudo-second-order kinetic and Langmuir isotherm models. Moreover, when MIL-101(Fe)@MgFe-LDH was applied for 300 mg kg−1 of Pb2+, Cd2+ and Cu2+ co-existing soil, the extremely low concentration of 1.24, 6.88 and 1.08 mg kg−1 for Pb2+, Cd2+ and Cu2+ can be reached in 7 days of column leaching experiment. Note that the release of Mg2+ from MIL-101(Fe)@MgFe-LDH was shown to promote pea seedling growth by acting as magnesium fertilizer. Detailed quasi-situ characterization and DFT calculation revealed the mechanism of isomorphic substitution of Mg2+ by Cu2+ accompanied by in-situ conversion to CuFe-LDH, while the formation of CdCO3 and Pb3(CO3)2(OH)2 can be demonstrated. Consequently, simultaneous super-stable mineralization of multiple heavy metals in water and soil can be accomplished.

Detection of myclobutanil and tebuconazole in apple using magnetic molecularly imprinted polymer surface-enhanced Raman spectroscopy

The main challenge in Raman detection of pesticide residues in agricultural products is matrix interference, which hinders accurate identification of trace compounds in complicated agricultural samples. In this study, a novel surface-enhanced Raman spectroscopy approach based on magnetic molecularly imprinted polymers (MMIP-SERS) was introduced for the rapid analysis of myclobutanil and tebuconazole in apples. The synthesized magnetic molecularly imprinted polymer selectively adsorbed triazole pesticides, effectively eliminating matrix interference in real samples. The saturation adsorption time for MMIPs was only 10 min. In addition, the synthesized colloidal gold served as an excellent substrate for enhancing the specific signals for myclobutanil and tebuconazole. We successfully identified the characteristic peak of tebuconazole at 1089 cm−1, while myclobutanil showed its characteristic peak at 632 cm−1. The series of experiments and recovery tests confirmed the high sensitivity of the developed MMIP-SERS method using colloidal gold as an enhanced substrate for fungicide analysis in apple samples. The linear detection ranges for myclobutanil and tebuconazole in apples were determined to be 0.2–10 mg/kg and 0.5–10 mg/kg, respectively. The limit of detection was 0.09 mg/kg for tebuconazole and 0.05 mg/kg for myclobutanil. This study provides a rapid and simple method for detecting myclobutanil and tebuconazole based on the synergistic effect of the imprinted polymer and SERS with good separation and detection performance.

Preparation of carboxyl-functionalized silica core-shell microspheres and their applications in weak cation exchange chromatography, heavy metal removal, and lysozyme enrichment.

Chromatography is a technique of separation based on adsorption and/or interaction of target molecules with stationary phases. Herein, we report the design and fabrication of BTDA@SiO2 core-shell microspheres as a new class of stationary phase and demonstrate its impressive performance for chromatographic separations. The silica microspheres of BTDA@SiO2 were synthesized by in situ method with 1,3,5-benzenetricarboxaldehyde and 3,5-diaminobenzoic to separate peptides and proteins on high-performance liquid chromatography. The BTDA@SiO2 core-shell structure has a high specific surface area and retention factor of 4.27 and 8.31 for anionic and cationic peptides, respectively. The separation factor and resolution were high as well. A typical chromatogram illustrated nearly baseline resolution of the two peptides in less than 3 min. The BTDA@SiO2 was also highly stable in the pH range of 1 to 14. Furthermore, the prepared BTDA@SiO2 core-shell material not only be used for chromatographic separation but also as heavy metal removal from water. Using a BTDA@SiO2, we also achieved a lysozyme enrichment with a maximum saturated adsorption capacity reaching 714mg/g. In summary, BTDA@SiO2 has great application prospects and significance in separation and purification systems.

In-depth study of adsorption mechanisms and interactions in the removal of pharmaceutical contaminants via activated carbon: a physicochemical analysis.

This study presents a theoretical analysis of the adsorption process of pharmaceutical pollutants, specifically acetaminophen (ATP) and diclofenac (DFC), onto activated carbon (AC) derived from avocado biomass waste. The adsorption isotherms of ATP and DFC were analyzed using a multilayer model, which revealed the formation of two to four adsorption layers depending on the temperature of the aqueous solution. The saturation adsorption capacities for ATP and DFC were 52.71 and 116.53mg/g, respectively. A steric analysis suggested that the adsorption mechanisms of ATP and DFC involved a multi-molecular process. The calculated adsorption energies (ΔE1 and ΔE2) varied between 12.86 and 22.58kJ/mol, with the highest values observed for DFC removal. Therefore, the adsorption of these organic molecules was associated with physisorption interactions: van der Waals forces and hydrogen bonds. These findings enhance the understanding of the depollution processes of pharmaceutical compounds using carbon-based adsorbents and highlight the potential of utilizing waste biomass for environmental remediation.

Adsorption Characteristics of Illite and Kerogen Oil Phase: Thermodynamics Experiments

In order to study the adsorption process and adsorption characteristics of shale oil at the macro scale, the isothermal adsorption experiments of illite and kerogen on a heptadecane (oil phase) solution were carried out by infrared spectrophotometry and gas chromatography–mass spectrometry. Based on the adsorption isotherm model and adsorption thermodynamic model, the characteristics of heptadecane adsorbed by illite and kerogen at different temperatures and oily solution concentrations were studied. The experimental results show that the concentration and temperature of the alkane solution help to enhance the adsorption and increase the saturated adsorption capacity. The difference is that the concentration will have a certain effect on the adsorption rate, while the temperature will not. Based on the three adsorption isotherm models, it was found that Langmuir and Freundlich were more suitable for describing the adsorption process of the heptadecane solution by illite and kerogen, and the adsorption characteristics of heptadecane molecules at different temperatures and adsorbents were evaluated. Heating leads to an increase in the collision efficiency between adsorbate molecules and adsorbents, thereby accelerating the migration rate of alkanes. Therefore, increasing temperature helps to enhance the adsorption capacity of rocks and increase the saturated adsorption capacity of minerals. The research results clarify the adsorption characteristics of shale oil heavy components from the macro level and fill the research gap in the application of solid–liquid isothermal adsorption physical experiments on the adsorption and occurrence of shale oil.

Low concentration adsorption of ammonia using metal halide loaded biogas residue-based carbon materials

Treating wastewater with elevated ammonia nitrogen levels in garbage treatment plants is a global concern, with blow-off recognized as an efficient process for nitrogen removal. However, this method generates low-concentration ammonia, presenting a challenge for adequate recovery. This study addresses this issue by impregnating metal halides onto K2CO3-activated biogas residue to create composite materials tailored for adsorbing low-concentration ammonia. We systematically investigated the impact of activation parameters, metal halide type, loading capacity, and environmental conditions on the adsorption properties of the materials. Notably, at an activation temperature of 700 °C, utilizing copper chloride with a loading capacity of 30 %, the material exhibited a saturation adsorption capacity of 29.32 mg/g for 200 ppm NH3, with a breakthrough time of 45.6 min, significantly surpassing the untreated sample and demonstrated excellent regeneration performance. SEM, BET, and FTIR analyses revealed that the material provided dispersion sites for metal halides, promoted the complexation of metal halides and ammonia and retained pores for ammonia diffusion, thereby enhancing adsorption efficiency. This innovative approach contributes to waste utilization and ensures efficient ammonia recovery through metal halide-ammonia complexation.

Mechanism of efficient adsorption for arsenic in aqueous solution by zeolitic imidazolate framework‑8.

Arsenic (As) is one extremely hazardous and carcinogenic metalloid element. Due to mining, metal smelting, and other human activities, the pollution of water (especially groundwater) and soil caused by As is increasingly serious, which badly threatens the environment and human health. In this study, a zeolite imidazolate framework (ZIF-8) was synthesized at room temperature and employed as an adsorbent to facilitate the adsorption of As(III) and As(V) from the solution. The successful synthesis of ZIF-8 was demonstrated by X-ray diffraction (XRD), and scanning electron microscopy (SEM) revealed that its particle size was approximately 80nm. The adsorption kinetics, adsorption isotherm, solution pH, dose, coexisting ions, and the synonymous elements antimony (Sb) were conducted to study the adsorption of As by ZIF-8 nanoparticles. The maximum saturation adsorption capacity was determined to be 101.47mg/g and 81.40mg/g for As(III), and As(V) at initial pH = 7.0, respectively. Apparently, ZIF-8 had a good removal effect on As, and it still maintained a good performance after four cycles. The coexisting ions PO43- and CO32- inhibited the adsorption of both As(III) and As(V). ZIF-8 performed well in removing both As and Sb simultaneously, although the presence of Sb hindered the adsorption of both As(III) and As(V). Both FTIR and XPS indicated the adsorption mechanism of As on ZIF-8: ZIF-8 generates a large amount of Zn-OH on the surface through hydrolysis and partial fracture of Zn-N, both of which form surface complexes with As.

Preparation and Characterization of Lignin‐Based Activated Carbon by Rubidium Chloride Chemical Method

AbstractIn order to prepare carbon adsorbent materials, lignin was used as raw material and rubidium chloride as activator, activated carbon materials were prepared by chemical activation method, and its structure was characterized and its adsorption performance on methylene blue solution was investigated; the adsorption of crystalline violet dye was carried out at different temperatures, and the adsorption thermodynamics was studied. The results showed that: the specific surface area of the activated carbon was 433.32 m2/g, the pore volume was 0.2191 cm3/g, and the average pore size was 2.0222 nm; the adsorption value of methylene blue could reach 172.0 mg/g, and it could quickly and efficiently adsorb methylene blue solution; the adsorption effect on crystal violet solution was good, and the saturated adsorption amount at 40 °C was up to 279 mg/g, and the removal rate reached 93 %, belonging to the spontaneous adsorption thermodynamic reaction. The experiment proved that rubidium chloride can be used as an activator to activate lignin raw materials to prepare activated carbon samples, and can effectively adsorb dyes.

Carboxylic acid modulated in situ growth of Zr-based MOFs on carboxylated cotton fabrics for removal of Cr(VI) from aqueous solutions

In this paper, carboxylated cotton fabric (CF-Ph-COOH) were obtained as active substrate by diazonium radical polymerization modification of cotton fibers. Then the MOF fabric composites were prepared by in situ growth of metal zirconium ions (Zr) and organic ligands on the surface of carboxylated cotton fabrics under carboxylic acid modifier. MOF fabric composites with controllable morphologies structures were achieved by regulating organic ligands, reaction time the type and dosage of regulator (formic acid and acetic acid). The prepared acetic acid regulated MOF fabric composites were designated as CF-HAc1-UiO-66, CF-HAc2-UiO-66, CF-HAc1-UiO-66-NH2, and CF-HAc2-UiO-66-NH2, respectively, and the formic acid regulated as CF-FA-UiO-66 and CF-FA-UiO-66-NH2. The fabricated carboxylic acid modulated MOF fabric composites were well characterized using SEM, TGA, XRD, FTIR, and XPS spectra. The adsorption experiment results show that carboxylic acid modulated Zr based MOF fabric composites can serve as adsorbent for effective removal of Cr(VI) from water, in which the CF-FA-UiO-66-NH2 was prepared under the ratio of ZrCl4 and BDC-NH2 is 1.006 and with 5.47 M formic acid regulator exhibits that the optimal adsorption efficiency and the removal efficiency is 79.5 %. In addition, the adsorption of Cr(VI) in water by CFA-UiO-66-NH2 showed a quasi-secondary kinetic model following the Langmuir adsorption model, showing a a typical of chemisorption. What’s more, the Cr(VI) removal efficiency and saturated adsorption capacity of CF-FA-UiO-66-NH2 was up to 80 % and 318.85 mg/g, respectively. The prepared CF-FA-UiO-66-NH2 MOF fabric composite was recyclable for removal of Cr(VI), and could be used as the potential adsorbent membrane for waste water treatment.

Preparation and Performance Study of Boron Adsorbent from Plasma-Grafted Polypropylene Melt-Blown Fibers.

In this study, the plasma graft polymerization technique was used to graft glycidyl methacrylate (GMA) onto polypropylene (PP) melt-blown fibers, which were subsequently aminated with N-methyl-D-glucamine (NMDG) by a ring-opening reaction, resulting in the formation of a boron adsorbent denoted as PP-g-GMA-NMDG. The optimal conditions for GMA concentration, grafting time, grafting temperature, and the quantity of NMDG were determined using both single factor testing and orthogonal testing. These experiments determined the optimal process conditions to achieve a high boron adsorption capacity of PP-g-GMA-NMDG. Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersion spectrum analysis (EDS), and water contact angle measurements were performed to characterize the prepared adsorbent. Boron adsorption experiments were carried out to investigate the effects of pH, time, temperature, and boron concentration on the boron adsorption capacity of PP-g-GMA-NMDG. The adsorption isotherms and kinetics of PP-g-GMA-NMDG for boron were also studied. The results demonstrated that the adsorption process followed a pseudo-second-order kinetic model and a Langmuir isothermal model. At a pH of 6, the maximum saturation adsorption capacity of PP-g-GMA-NMDG for boron was 18.03 ± 1 mg/g. In addition, PP-g-GMA-NMDG also showed excellent selectivity for the adsorption of boron in the presence of other cations, such as Na+, Mg2+, and Ca2+, PP-g-GMA-NMDG, and exhibited excellent selectivity towards boron adsorption. These results indicated that the technique of preparing PP-g-GMA-NMDG is both viable and environmentally benign. The PP-g-GMA-NMDG that was made has better qualities than other similar adsorbents. It has a high adsorption capacity, great selectivity, reliable repeatability, and easy recovery. These advantages indicated that the adsorbents have significant potential for widespread application in the separation of boron in water.

Adsorption properties of Pb(II) and Cd(II) in acid mine drainage by oyster shell loaded lignite composite in different morphologies

A new idea to alleviate environmental pollution is the development of low-cost adsorbents using natural minerals and fishery wastes to treat high concentrations of heavy metal pollutants in acid mine drainage (AMD). Adsorbent morphology, adsorptive and regenerative capacity, and application potential are limiting factors for their large-scale use. Oyster shells capable of releasing alkalinity were loaded on the surface of lignite to develop two composite adsorbents with different morphologies (powdery and globular) for the treatment of AMD containing Pb(II) and Cd(II). The results show that the ability of the adsorbent to treat AMD is closely related to its morphologies. The pseudo-second-order kinetic model and the Langmuir model are suitable to describe the adsorption process of OS-M(P), and the maximum adsorption saturation capacities of Pb(II) and Cd(II) are 332.6219 mg/g and 318.9854 mg/g, respectively. The pseudo-second-order kinetic model and the Freundlich model are suitable to describe the adsorption process of OS-M(G). A synergistic result of electrostatic adsorption, neutralization precipitation, ion exchange and complex reaction is achieved in the removal of Pb(II) and Cd(II) by two morphologies of adsorbents. The regeneration times (5 times) and recovery rate (75.75%) of OS-M(G) are higher than those of OS-M(P) (3 times) and recovery rate (20%). The ability of OS-M(G) to treat actual AMD wastewater is still better than that of OS-M(P). OS-M(G) can be used as a promising environmentally friendly adsorbent for the long-term remediation of AMD. This study provides a comprehensive picture of resource management and reuse opportunities for natural mineral and fishery wastes.

Study on the adsorption of Ce(III) on phosphonic acid functionalized ZIF-67@SiO2 magnetic porous carbon materials

A ZIF-67 composite SiO2 material (ZIF-67@SiO2) was synthesized using ethyl orthosilicate (TEOS) as a silicon source, followed by one-step carbonization to produce magnetic porous nitrogen-doped carbon material (MNPC@SiO2) using ZIF-67@SiO2 as a carbon precursor. Subsequently, the composite P-MNPC@SiO2 was obtained through functionalization with diethylphosphonoethyltriethoxysilane (DPTS), and its characteristics were analyzed. The adsorption properties of Ce(III) on MNPC@SiO2 and P-MNPC@SiO2 composites were investigated under various conditions through adsorption experiments. Kinetic, isothermal, and thermodynamic models were employed to analyze the adsorption mechanism of P-MNPC@SiO2 on Ce3+ and assess adsorbent stability and regeneration performance. The result shows that P-MNPC@SiO2 exhibited excellent adsorption capacity for Ce3+ and possessed magnetic properties conducive to recycling. Under optimized conditions, P-MNPC@SiO2 reached Ce(III) adsorption saturation within 20 min, with a maximum adsorption capacity of 342.52 mg/g, which was 1.9 times higher than that of the MNPC@SiO2 material. Data fitting shows that surface adsorption controls the rate-limiting step, and Ce(III) forms a monolayer adsorption on the surface of the adsorbent material. Furthermore, P-MNPC@SiO2 exhibits strong stability and regeneration properties.

Ionic liquid-functionalized transition-metal oxides as highly recyclable and efficient nano-adsorbent for fluoride removal

The modification of functionalized ionic liquids into sewage adsorbents addresses key limitations of traditional adsorption methods, offering enhanced selectivity, good adsorption, and renewability. In this work, imidazole-amino ionic liquid was successfully modified into transition-metal oxide CuOX through coordination interactions between the imidazole ring and Cu+. Most importantly, specific and thermal-responsive hydrogen bonds between amino and fluoride exhibited excellent selectivity for capturing fluorine while providing effective renewability through thermal activation. As expected, the adsorbents exhibited a rapid adsorption rate in fluorine solution (adsorption saturation time tS = 38 h, fluoride concentration 2 mg·L−1) and significant adsorption capacity (maximum adsorption capacity qm = 337.8 mg·g−1, 293 K). Moreover, a recovery rate was exceeded 95 % after incubation with the boiling water. As for industrial application, the adsorbent demonstrated an impressive fluoride removal efficiency exceeding 80 % and a remarkable recovery rate exceeding 70 % when treating wastewater from the photovoltaic cell and semiconductor industry. This not only significantly reduced expenses associated with wastewater treatment but also alleviated the incidence of secondary pollution. By offering a recyclable and effective solution for sewage adsorbents, this strategy holds promise for addressing water pollution challenges in industrial settings.

Solvent-free synthesis of defective Zr-based metal–organic framework from waste plastic bottles for highly efficient lomefloxacin removal

Large amount of polyethylene terephthalate (PET) plastics waster and emerging contaminants in water, including fluoroquinolone antibiotics, pose challenges to human survival. In this work, a green synthesis scheme is proposed in which the defective UiO-66 (d-UiO-66) is fabricated via a solvent-free routine by using PET plastics waster as raw materials for lomefloxacin (LOM) removal. In comparison with defect-free UiO-66, the created defect imparts d-UiO-66 with higher porosity and abundant defective Zr sites, which are beneficial to boost LOM adsorption. As expected, d-UiO-66 exhibited excellent LOM adsorption performances, showcasing a saturation adsorption capacity of 588 mg g−1 and a kinetic rate constant of 0.204 g mg−1 h−1, which are 3.5 and 2.0 times higher than those of the pristine UiO-66, respectively. Remarkably, the LOM saturation adsorption capacity of d-UiO-66 surpasses that of all reported adsorbents. Mechanism study reveals that this outstanding adsorption performance of d-UiO-66 is mainly ascribed to the abundant defective sites, high porosity, together with the strong hydrogen bonding interaction and π-π stacking interaction between d-UiO-66 and LOM. Therefore, the d-UiO-66 obtained by the solvent-free method can not only effectively upcycle PET plastic waster, but also efficiently remove LOM, demonstrating a potential routine to simultaneous address the solid PET waster and wastewater.

Resources recovery-rubidium recovery from desalination brine through hydrometallurgy techniques

Because of the water scarcity in many regions, different methods have been implemented to address this problem. The desalination technique is known as a practical solution among them. However, brine from the desalination process, which contains high concentrations of salts, minerals, and chemicals, will cause environmental harm to the sea, soil, and groundwater if it is not properly treated. Therefore, recovering critical resources from brine is essential for reducing brine disposal. This study aims to apply two hydrometallurgy systems, namely ion exchange and ionic liquid extraction, to circulate rubidium resources from brine. Dowex G26 resin was employed in the ion exchange system, and the adsorption isotherm model and saturated adsorption capacity were explored initially. The optimal parameters such as pH value, L/S ratio (liquid/solid), adsorption period, and adsorption temperature will then be investigated. In the ionic liquid extraction process, the t-BAMBP/C2mimNTf2 system (4-tert-Butyl-2-(α-methylbenzyl) phenol/1-ethyl-3-methylimidazolium bis(trifluoromethyls​ulfonyl)​imide) was used, and the parameters including pH value, concentrations of t-BAMBP, (O + I)/A ratio (organic + ionic liquid/aqueous), extraction time, and extraction temperature will be optimized as well. The results reveal that adsorption capacity and extraction efficiencies were 14.3 mg g− 1 and 86%, respectively. Furthermore, suitable reagents, including HCl and HNO3, were applied to desorb and strip rubidium from the Dowex G26 and t-BAMBP/C2mimNTf2 systems. To sum up, environmental hazards of desalination brine and rubidium resources can be reduced and recovered through the two different extraction systems.

Utilizing Activated Carbon Nanopores for Electrochemical Oxidation of Perylene to Redox-Active 3,10-Perylenedione: Application in Electrochemical Capacitor Electrodes.

We demonstrate that nanopores of activated carbon (AC) function as nanoreactors that oxidize perylene (PER) to a redox-active organic compound, 3,10-perylenedione (PERD), without any metal catalysts or organic solvents. PER is first adsorbed on AC in the gas phase, and the PER-adsorbed AC is subjected to electrochemical oxidation in aqueous H2SO4 as the electrolyte. Because gas-phase adsorption is solvent-free, PER is completely adsorbed on AC as long as the amount of PER does not exceed the saturated adsorption capacity of the AC, which enables accurate control of the amount adsorbed. PER is electrochemically oxidized to PERD in the nanopores of AC at above 0.7 V vs Ag/AgCl. The hybridized PERD undergoes a rapid reversible two-electron redox reaction in the nanopores owing to the large contact interface between the conductive carbon pore surfaces and PERD. The resulting AC/PERD hybrids serve as electrodes for electrochemical capacitors, utilizing the rapid redox reaction of PERD. The hybridization method is advantageous for quantitatively optimizing electrochemical capacitor performance by adjusting the amount of adsorbed PER. Moreover, because PERD hybridization in the AC nanopores does not expand the electrode volume, the volumetric capacitance increases with increasing hybridized PERD content. In three-electrode cell measurements, the volumetric capacitance at 0.05 A g-1 reaches 299 F cm-3, and 61% of this capacitance is retained at 10 A g-1 when 5 mmol of PER is used per gram of AC. Meanwhile, pristine AC delivers 117 F cm-3 at 0.05 A g-1 with a capacitance retention of 46% at 10 A g-1. Two-electrode cell measurements reveal that self-discharge is significantly suppressed by the hybridized PERD when AC/PERD hybrids and AC are used as cathodes and anodes, respectively, compared to that of a symmetrical AC cell. Moreover, PERD does not undergo cross-diffusion in the asymmetrical cells during self-discharge tests for 24 h.