Adsorption Technology Research Articles

Unlocking the potential of environmentally friendly adsorbent derived from industrial wastes: A review.

With increasing urbanization and industrialization, growing amounts of industrial waste, such as red mud (RM), fly ash (FA), blast furnace slag (BFS), steel slag (SS), and sludge, are being produced, exposing substantial threats to the environment and human health. Given that numerous researchers associate with conventional adsorbents, developing and utilizing industrial wastes derived from adsorption technology still has received limited attention. Utilizing this waste contributes to developing alternative materials with superior performance and significantly reduces the volume of solid waste. The excellent physical and chemical characteristics of these wastes are also investigated in this paper. This review attempts to demonstrate a comprehensive overview of the application of industrial waste-based adsorbent in the adsorption process for removing organic pollutants, dyes, metallic ions, non-metallic ions, and radioactive substances. In addition, industrial waste-based adsorbents are among the most promising and applicable techniques for pollutant removal, offering remarkable adsorption efficiency, rich surface chemistries, reasonable cost, simple operation, and low energy consumption. This review summarizes state-of-the-art advancements in engineered adsorbents (including physical and chemical modifications). It provides a holistic view regarding a comprehensive understanding of the mechanism involved in adsorption for water remediation. The challenges and the prospects for future research in applying these adsorbents are also elucidated, contributing to sustainable waste management and environmental sustainability.

Adsorbent Properties of Porous Boron Nitride and Activated Carbon: A Comparative Study.

Porous boron nitrides possess beneficial properties such as high thermal and chemical stability which are critical for applications in adsorption processes. In order to assess possible fields of applications, trace-level adsorption isotherms of different hydrocarbons on two synthesized porous boron nitrides and two commercial activated carbons are compared. By normalizing the adsorptive loadings on the micropore surface area, superior adsorption performances of the BN materials on polar and aromatic adsorptives with up to 50% higher loadings compared to the activated carbons can be shown. Nonpolar adsorptives, on the other hand, feature higher specific loadings on the activated carbon. Consequently, the size of the micropore surface appears to be decisive for nonpolar adsorptives, while the higher polarity of the boron nitrides is the dominant influencing factor for the adsorption of polar and aromatic components. For an energetic study of the adsorbents, calorimetric experiments were performed to identify and discuss adsorbent-adsorptive interactions. While the initial heat of adsorption of the nonpolar n-hexane is lower on the boron nitride than on the activated carbon due to a less favorable spatial arrangement, toluene shows comparable values on both adsorbent classes and the polar acetone shows higher values on the polar boron nitride. Considering technical applications in adsorption technology, the thermal stability of the boron nitrides is investigated using spontaneous ignition temperatures and points of initial oxidation. Here, the porous boron nitrides with oxidation temperatures above 900 °C show about 400 °C higher values and thus a significantly higher thermal stability.

DFT based investigations on inherent CO2 adsorption and direct dissociation capability of Ti2C and Nb2C mxenes

Transition metal carbide MXenes, specifically Ti2C and Nb2C, have been investigated for their ability to efficiently adsorb and dissociate CO2 using First Principles Calculations based on Density Functional Theory (FPS-DFT). Pure Ti2C and Nb2C sheets were studied with the adsorption of 1 to 4 CO2 molecules, and the results were analyzed for each case. For 4 CO2 molecules adsorbed on Ti2C and Nb2C sheets, the weight percentage (wt%) ratio was found to be 21.39% and 14.33%, respectively. The Density of States (DOS) analysis revealed that, upon CO2 adsorption, the CO2 molecule dissociates into CO and O atoms on the MXene surface. The CO molecule showed no significant hybridization with the host sheet atoms, whereas the O atom exhibited strong hybridization with the MXene surface. Transition State (TS) profiles illustrated the dissociation steps on both Ti2C and Nb2C surfaces. Phonon calculations confirmed the dynamic stability of both pure and CO2 adsorbed MXenes. Molecular Dynamics (MD) simulations conducted at 900 K indicated uniform temperature and Mean Square displacement (MSD) profiles, suggesting the stability of both pure and CO2 adsorbed MXenes at elevated temperatures, as well as uniform CO2 adsorption behavior. The adsorption energies for Ti2C and Nb2C sheets were calculated to be in the range of -1.89 to -2.77eV, suggesting that the adsorption process is favorable, spontaneous, and predominantly involves chemisorption. These findings indicate that Ti2C and Nb2C MXenes, in their intrinsic forms, are promising candidates for CO2 adsorption and dissociation technologies.

Hierarchical pore-enhanced ion transport and defect-induced dual strong interactions for highly efficient lithium extraction

In the past decade, adsorption method has attracted great attention on the lithium extraction. The key issue in adsorption technology is to develop adsorbents with high adsorption capacity, selectivity, and recycle-stability. Here, the highly efficient metal–organic framework adsorbents were developed for lithium extraction, which were fabricated by the in-situ conversion of MIL-121 in alkali solution. The adsorbent after acid activation, termed as H-CAOMIL, was featured with the hierarchical porosity, enhanced density of free carboxylic groups, and exposed aluminum-oxygen defect sites to enhance the ion transport and provide dual strong interaction for Li+. H-CAOMIL exhibited the remarkable Li+ adsorption capacity (QLi+ = 5.28 mg/g) and selectivity (αKLi = 21.33, αNaLi= 9) from low-concentration lithium-containing solutions. Moreover, the H-CAOMIL can be easily regenerated in weakly acidic solution. Impressively, Li+ adsorption capacity retained at 92 % of the initial capacity even after five adsorption–desorption cycles. Furthermore, the comprehensive characterizations and theoretical calculations indicated that the specific coordination of COO-Li and AlO-Li played a crucial role in the recovery capacity and selectivity of Li+. This work offers precious insights for the future exploration of highly efficient adsorbents for lithium extraction.

Enhanced VOCs adsorption on Group VIII transition metal-doped MoS2: A DFT study

Volatile organic compounds (VOCs) represent a significant category of toxic and harmful air pollutants. Among the various abatement techniques available for VOCs, adsorption technology is widely recognized as a cost-effective solution. In this study, density functional theory (DFT) was employed to calculate and compare the adsorption capacities of six typical VOCs on pristine MoS2 and MoS2 modified with Group VIII (MVIII) transition metals atoms. It is found that MVIII-MoS2 monolayer demonstratesa significant enhancement in adsorption capabilities for VOCsrelative to pristine MoS2. Among these Group VIII transition metals atoms, Fe, Ru and Os atoms exhibited the most significant VOCs adsorption enhancement, with Fe atoms demonstrating a particularly pronounced effect. This suggests a synergistic interaction between the metal dopants and the substrate. Density of states (DOS) and charge density difference analyses provided further insights into the mechanisms underlying improved adsorption capability. Interestingly, the introduction of MVIII atoms results in the emergence of a novel state density within the surface state of MoS2, thereby facilitating enhanced electron transfer between VOCs and the substrate. Charge density difference calculations further corroborated these findings, with certain configurations exhibiting significant electron cloud overlap. Such modification leads to more active electron transfer, thereby increasing the substrate’s affinity for VOC molecules and consequently improving the adsorption efficiency. The findings not only enhance the comprehension of VOC adsorption mechanisms on MoS2 but also underscore the potential of metal-doped two-dimensional materials for environmental applications.

Highly efficient MIL-53(Al)@Biomass hybrid for oxytetracycline elimination: Adsorption, LED-induced photocatalysis and pyrolytic recycling

The presence of antibiotics in water discharges represents a hazard for the ecosystems, as it could affect the biota equilibrium at the micro and macroscales. Consequently, it is crucial to develop effective adsorption and oxidation technologies to remove antibiotics from water. Herein, we assessed the effectivity and stability of a metal organic framework-biomass hybrid (MIL-53(Al)@RH) for the removal of oxytetracycline (OTC) via adsorption and photocatalytic degradation. Under equilibrated conditions, the hybrid retained 165mgg−1 OTC. When adsorption and photocatalytic degradation were arranged in tandem, the system removed 99% of OTC with a dose of 2.83mg H2O2/mg OTC. The thermo-kinetic interpretation of the adsorption measurements was well described by Sip´s isotherm and pseudo-second kinetic models, which along with the heat of adsorption (−104.8kJmol−1) suggest a chemical interaction between the OTC and MIL-53(Al)@Rice Husk hybrid active centres. The MIL-53(Al)@RH hybrid demonstrated a remarkable stability with an OTC removal above 90% after 10 operational cycles. Moreover, pyrolysis of OTC-saturated hybrid led to a carbonaceous structure which demonstrated an outstanding OTC adsorption capacity (221mgg−1 OTC). The results demonstrate that the MIL-53(Al)@RH hybrid presents a significant prospect for combined adsorption-photocatalytic treatment of water bodies contaminated with antibiotics.

Experimental study of four-step thermal swing adsorption cycle to upgrade biogas obtained from anaerobic digestion

Biogas is a renewable source of energy that when upgraded can be adopted as a reliable and sustainable alternative. This study evaluates the performance of thermal swing adsorption technology applying resistive heating, in upgrading biogas obtained from anaerobic digestion to biomethane. Commercial coconut shell-based activated carbon was used as an adsorbent in the four-step cycle process to capture carbon dioxide, using a fabricated adsorption model. The influence of minor gas constituents of biogas in carbon dioxide breakthrough curves was analyzed. Dynamic adsorption tests were carried out to evaluate the system performance in carbon dioxide capture. The maximum regeneration temperature of 60 ℃ was found to have peak carbon dioxide concentration of 39% in the waste gas, maximum energy requirements of 0.1538kWh per cycle, and an energy efficiency of 87%. This is a good trade-off between adsorbent recovery and system energy efficiency. The adoption of thermal swing adsorption technology in biogas upgrading systems is a viable alternative for water-deficient regions.

Facile synthesis and biomimetic amine-functionalization of chitosan foam for CO2 capture

A high-performance biomass-based adsorption materials could be the promising trend for CO2 capture and storage technology. However, the direct application of biomass-based porous materials as a CO2 adsorbent with enhanced performance is an emerging issue. Herein, a facile synthesis and a biomimetic strategy were combined to prepare amine-functionalized chitosan foam for CO2 capture, and then a porous biomass is achieved for the application on the environment protection field. Firstly, the chitosan foam was synthesized by the emulsion-templating method at room temperature. Depended on stabilizing n-octane in the chitosan hydrogel with Span 80, a tunable three-dimensional network porous structure was obtained. Subsequently, co-deposition with dopamine (DA) and polyethyleneimine (PEI) was applied to load abundant amine content on the surface of chitosan foam and thereby improving CO2 adsorption capacity. Finally, the as-prepared amine-functionalized chitosan foam exhibited the impressive adsorption capacity of 3.59 mmol/g at 333 K and atmospheric pressure, and the better adsorption selectivity and stability. The results extend the preparation approach of biomass porous materials, and also its application in CO2 adsorption technology.

Amidation modified hollow composite microspheres as a self-floating adsorbent for efficient capture of anionic dye DB86 and heavy metal nickel (II).

The co-contamination of dyes and heavy metal ions often used as mordants poses potential risks to environment and public health, and is a challenging problem that needs to be solved in water treatment. Meanwhile, improving the solid-liquid separation capability of adsorbents is of great significance for the application of adsorption technology. Herein, amidation modified hollow composite microspheres were prepared using hollow glass microsphere (HGM) as matrix through hydrolysis and condensation of silane coupling agent (A-1100) and subsequent amidation reaction. The material (HGMNE) not only exhibited good adsorption performance for DB86 and Ni2+ but also had stable self-floating capability. The adsorption of DB86 by HGMNE is mainly carried out by the electrostatic interaction between positively charged quaternary amine nitrogen and negatively charged DB86, while the adsorption of Ni2+ is achieved by the carboxyl group in EDTA group through complexation interaction to adsorb Ni2+ to form Ni complex. This research not only is devoted to the utilization of HGMNE to achieve the co-removal of DB86 and Ni2+ and flexible self-floating solid-liquid separation but also verifies the feasibility and applicability of the modification method of introducing organic adsorption functional groups through amidation reaction, so as to expand the preparation path of HGM-based adsorbents.

Unveiling Temperature-Induced Structural Phase Transformations and CO2 Binding Sites in CALF-20.

The increase in atmospheric carbon dioxide concentration linked to climate change has created a need for new sorbents capable of separating CO2 from exhaust gases. Recently, an easily produced metal-organic framework, CALF-20, was shown to withstand over 450,000 adsorption/desorption cycles in steam and wet acid gases. Further development and industrial application of such materials require an understanding of the observed processes. Herein, we demonstrate that conditioning as-synthesized CALF-20 single crystal transforms it into a different phase, γ-CALF-20. The transformation resulted in significant structural changes, including the binding of water molecules to Zn(II), accompanied by a reduction of 9% in the unit cell volume. Our experimental findings were supported by the energy-volume dependence of CALF-20 in the presence and absence of water molecules calculated from density functional theory. We have also monitored the sorption process of the dominant greenhouse gas, CO2, on the initial phase of CALF-20 at atomic resolution using in situ single-crystal X-ray diffraction under specific pressure. The new understanding of CALF-20 chemistry from these studies should facilitate development of novel sorbents for gas adsorption technologies.

A novel magnetic S/N co-doped tea residue biochar applied to tetracycline adsorption in water environment

The issue of tetracycline (TC) contamination has attracted widespread attention. Adsorption technology has great potential for application in the field of TC remediation. This study achieved the production of nitrogen self-doped biochar using waste tea leaves as raw materials, and further improved its TC removal effect by doping sulfur elements. A recyclable high-performance TC adsorbent magnetic S/N co-doped tea residue biochar (MSNB) was obtained through ferromagnetic modification, which could be used as an effective TC adsorbent. The effects of MSNB dosage and initial solution pH on TC removal were evaluated. The recovery performance of MSNB adsorbent on TC was studied. The maximum adsorption performance at 298 K calculated using the Langmuir model was 140.76 mg g−1. The fitting results of adsorption kinetics indicated that chemical adsorption was the main factor affecting the adsorption reaction. After 5 cycles of adsorption, the removal of TC by MSNB remained above 88.30 %. This study could provide theoretical support for the treatment of tetracycline wastewater by biochar adsorption.

Investigation on novel chitin and chitosan from dung beetle Heteronitis castelnaui (Harold, 1865) and its potential application for organic dyes removal from aqueous solution

Chitosan, a natural polysaccharide, has attracted considerable attention as an environmentally friendly and highly efficient adsorbent for dye removal. It is usually produced by deacetylation or partial deacetylation of chitin. However, conventional sources of chitin and chitosan are limited, prompting the need for alternative sources with improved adsorption capabilities. Herein, this study focuses on exploring a novel chitin and chitosan source derived from the dung beetle and evaluates its potential for organic dye removal from aqueous solutions. The research involves the extraction and characterization of chitin and chitosan from dung beetle Heteronitis castelnaui (Harold, 1865) using various analytical techniques, including SEM, FT-IR, TGA, XRD, NMR, deacetylation degree and elemental analysis. The chitosan obtained was used for the formation of hydrogels with sodium alginate via cross-linking with calcium chloride. And then the prepared hydrogels were evaluated for its adsorption capacity through batch adsorption experiments using methylene blue as a model pollutant. The adsorption capacity for methylene blue was 1294.3 mg/g at room temperature with solution pH = 12, MB concentration of 1800 mg/L. Furthermore, the kinetics of the adsorption process were analyzed using pseudo-first-order and pseudo-second-order models to understand the rate of adsorption. The maximum adsorption capacities were determined using Langmuir and Freundlich isotherm models. This study provides valuable insights for the development of sustainable dye adsorption technologies, specifically investigating a novel chitosan source derived from the dung beetle.

A multi-node thermodynamic model on temperature-vacuum swing adsorption (TVSA) for carbon capture: Process design and performance analysis

The adsorption technology plays a significant role in the carbon capture domain for mitigating the CO2 emissions, whereas the heterogeneous character is presented in practical adsorption process. In this study, a multi-node thermodynamic model is established for temperature-vacuum swing adsorption (TVSA) considering the end non-uniform adsorption. It shows superior performance for the assessment of practical TVSA cycle compared with lumped model. Through the influence analysis of different operation parameters based on multi-node model, specific exergy consumption increases from 41.6 to 62.4 kJ/mol caused by simultaneous drop of heat consumption and lift of work consumption as feed pressure raises from 1.0 to 3.0 bar. Exergy efficiency ranges between 13.8 % and 15.0 % as CO2 concentration increases from 10 % to 20 %. However, those under ppm-level are below 0.86 %, presenting the higher exergy consumption but lower desorption capacity represented for direct air capture. The heat consumption of front half part of adsorption bed is 39.7 % higher than the latter one, proving the potential cascaded desorption of subzone heating is superior for reducing the energy consumption. Furthermore, exergy consumption is lifted due to enhancement of work consumption of vacuum pump as vacuum pressure reduces from 1.0 to 0.02 bar, resulting exergy efficiency drops from 19.6 % to 13.4 %.

Synergistic Enhancements of Zn-ZIF with Nano Zinc Oxide for Hydrogen adsorption, energy storage, and photocatalytic technologies

Creating the porous Zinc-Zeolitic Imidazolate Framework (Zn-ZIF) using a solvothermal technique addresses the need for advanced materials with distinctive properties and cost-effectiveness in modern applications. The PXRD, SEM, UV-DRS, TEM, and TGA/DTG are used to characterize different concentrations of Zn-ZIF. Zn-ZIF's crystalline structure and phase purity have been verified by PXRD. Using diffuse reflectance spectra, the Kubelka-Monk function determined the band gaps of the Zn-ZIF samples, and scanning electron microscopy revealed a more porous structure. At 77 K and 1 bar, the Zn-ZIF solution with a 2:1 ratio had the highest hydrogen storage capacity (1.71 wt%). The electrochemical behavior of several Zn-ZIF electrodes in a 6 M KOH electrolyte was evaluated by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) experiments. The Zn-ZIF electrode with a 2:1 ratio exhibits a low charge transfer resistance and a high proton diffusion coefficient (D) of 1.687 × 10−4 cm2 s−1. The characteristics of the 2:1 synthesized Zn-ZIF electrode as a supercapacitor were investigated. Our analysis of the generated Zn-ZIF material's specific capacitance values after 2000 cycles revealed an impressive retention rate of nearly 89 %, with values of 296.6 Fg-1. In addition, we examined the photocatalytic activities of the as-synthesized material by exposing it to ultraviolet light and seeing how it degraded organic dyes such as Cango-Red (CR) dye. With a photocatalytic efficacy of 95.06 % for CR dye, Zn-ZIF (2:1 ratio) is the most effective. These findings should provide new knowledge for researchers interested in developing novel Zn-ZIF materials for photocatalytic, energy storage, and hydrogen storage applications.

Exploring the thermodynamics and dynamics of lithium ions inserted into Li1-xMn2O4 electrode at different temperatures

Efficient lithium extraction via electrochemical adsorption holds great promise for resource utilization and energy storage. However, the mechanism of how temperature influences the electrochemical adsorption process, particularly the thermodynamics and dynamics in the liquid, liquid–solid interface, and solid remains unclear. To address this challenge, we explored the impact of temperature (273.15 to 328.15 K) using Li1-xMn2O4 as an adsorbent. For the liquid phase, the conductivity increased from 0.89 to 0.95 S/m following lnΛ = -0.11(1000/T) + 0.27 in thermodynamics; the solution viscosity decreased from 1.71 × 10-3 to 5.15 × 10-4 Pa·s conforming lnη = 1.96(1000/T) − 13.54 in dynamics. For the liquid–solid interface, the charge transfer resistance (Rct) decreased from 42.03 to 25.17 ohm obeying ln(1/Rct) = -0.82(1000/T) − 0.69 in thermodynamics; the exchange current (i0) showed a positive correlation with temperature in fitting Logi0 = -0.50(1000/T) − 1.40 in dynamics. For the solid phase, the increase in reduction peak voltage (ERP) and the decrease in Gibbs free energy (G), entropy (S), and enthalpy (H) all indicate that the increase of temperature promotes lithium ions to inserted into Li1-xMn2O4 in thermodynamics; the increased diffusion coefficient (DLi+(S)) and higher reduction peak current (IRP) suggest that higher temperature strengthens lithium ions diffusion and insertion in dynamics. In the temperature range, the adsorption capacity gradually increased from 1.15 to 7.37 mg/g, the initial current enhanced from −3.40 × 10-4 to −1.85 × 10-3 A, the terminal current raised from −1.59 × 10-4 to −7.40 × 10-4 A, and the current efficiency improved from 31.28 % to 66.11 % in the temperature range. This work provides a deeper understanding of the impact of temperature on the electrochemical lithium adsorption process from thermodynamics and dynamics. This work also offers crucial guidance for the upgrading of electrochemical lithium adsorption technology and can be applied to other fields such as energy storage, catalysis, and synthesis, providing a valuable reference for optimizing reaction parameter design in thermodynamics and dynamics.

A porous phenolic resin sorbent for enhanced CO2 capture: Synthesis, optimization, and techno-economic analysis

Amidst rising global concerns about climate change, the capture and sequestration of carbon dioxide (CO2) from industrial emissions is becoming increasingly critical. In the present study, a phenolic resin-based porous polymer for CO2 capture is developed, offering a solution to the dual challenges of efficacy and cost in current carbon capture technologies. Optimization of synthesis parameters, including temperature, reaction time, and catalyst amount was performed using response surface methodology (RSM) to maximize surface area and economic benefits. The optimized polymer demonstrated a substantial CO2 adsorption capacity of 3.06 mmol/g at 273 K and 1 bar, with a specific surface area of 860 m2/g. An early-stage techno-economic analysis of sorbent synthesis was conducted, relating cost to sorbent quality and surface area. It was found that producing the polymer at low temperatures is more cost-effective, while synthesis at higher temperatures offers operational advantages. This research addresses a gap in existing literature by focusing on the sorbent material and its economic viability, paving the way toward the commercialization of such adsorption technology.

Efficient removal of methylene blue by a biochar from neem tree shell wastes using adsorption technology

Efficient removal of methylene blue by a biochar from neem tree shell wastes using adsorption technology

Selective adsorption of divalent and trivalent cations in porous electrodes.

The capacitive deionization technology uses the electrochemical adsorption of ions in porous electrodes to desalinate seawater or brackish water. Recently, capacitive deionization has gained significant attention as a technology for selective adsorption of ionic species from multicomponent aqueous electrolytes. To investigate the mechanism of selective adsorption at the molecular level, we performed molecular dynamics simulations of aqueous electrolytes and porous electrodes with different divalent or trivalent ions, electrode pore sizes, and applied voltages. We calculated the free energy barriers preventing ions from entering the pores of the electrode and the structure of the water molecules near the ions and the electrode surface under various conditions. Our results suggest that, when the pore and ion sizes are comparable, the steric and electrostatic interactions between the hydrated ions and electrode pores are comparable in magnitude. Moreover, the relative importance of the two interactions can be reversed by slight changes in the external conditions, such as the ion size, valence of the ions, electrode pore size, and applied voltage. Thus, by finely tuning the electrode pore size and the applied voltage, it may be possible to selectively adsorb a particular ionic species from a multicomponent electrolyte through capacitive deionization using a porous electrode.

Breakthrough curves of H2/CO2 adsorptions on CuBTC and MIL-125(Ti)_NH2 predicted by empirical correlations and deep neural networks

With the continuous emergence of new materials, efficiently screening suitable materials for hydrogen purification by pressure swing adsorption (PSA) technology has become a hot topic. Metal-organic frameworks (MOFs) hold significant promise in gas adsorption and separation due to their unique structure and versatility. Breakthrough curves depict the dynamic adsorption kinetics of multi-components in fixed-bed columns, offering a means to screen adsorbents. In this study, a deep neural network (DNN) model comprising 11 hidden layers is developed to predict the dynamic breakthrough behavior of MOF CuBTC and MIL-125(Ti)_NH2 adsorbents. The training data for the DNN were generated from a non-isothermal model established using Aspen Adsorption software. Results demonstrate that the DNN model effectively predicts the H2/CO2 breakthrough behavior on CuBTC and MIL-125(Ti)_NH2 adsorbents. Compared with empirical mathematical correlation models, the DNN can predict breakthrough profiles under varying operating conditions, exhibiting superior adaptability. Furthermore, parametric studies based on the DNN model reveal that initial temperature, adsorption pressure and feed flow rate play important roles in the dynamic adsorption process, significantly influencing the position and shape of the breakthrough curve. Decreasing the feed flow rate and initial temperature while increasing adsorption pressure can enhance breakthrough times and hydrogen purity. By comparing the breakthrough curves of the two adsorbents under different operating conditions for H2/CO2, the dimensionless breakthrough time of CO2 on the CuBTC adsorbent was longer. Additionally, simulation results of the PSA cycle suggest that CuBTC yields higher hydrogen purity than MIL-125(Ti)_NH2. Consequently, CuBTC is deemed more suitable for hydrogen purification of binary H2/CO2 mixtures than MIL-125(Ti)_NH2.

Synthesis and VOCs adsorption properties of Diatomite/FAU-type zeolite composites

Adsorption technology utilizing zeolites as adsorbents is a highly efficient and cost-effective method for controlling the emission of volatile organic compounds (VOCs). Herein, two hierarchical diatomite/FAU-type zeolite composites were synthesized by a seeding-assisted secondary hydrothermal growth method and high-temperature hydrothermal dealumination, respectively. The adsorption properties of the composites for VOCs, such as toluene, ethyl acetate, n-heptane, methanol and acetone, were systematically evaluated. The pseudo-second-order model provided a perfect fit to adsorption kinetics, while the Langmuir model agreed the best with the adsorption isotherms. Furthermore, Dt/USY has remarkable recycling stability even after five regeneration cycles, resulting in outstanding VOCs adsorption efficacy.