High BET Surface Area Research Articles

Unraveling lithium-ion intercalation in lead-free bismuth-based vacancy ordered halide perovskites supercapacitors

Halide perovskites have recently gained a lot of attention in energy storage applications because of their unique properties. The difficulty in getting high-performance supercapacitors requires the significant development and customization of electrode materials. This study explores vacancy-ordered lead-free halide perovskites with chemical formula A3B2X9 as electrode material for supercapacitors. Furthermore, we have tuned the X site (X = Br−, Cl−, I−) to see the effect of halide ions on supercapacitor performance. Due to high ionic mobility and BET surface area, Cs3Bi2I9 has a specific capacitance of ∼242 F/g and energy density of ∼140 Wh/kg; however, power density variation is almost the same for all samples, measured in three-electrode systems. We have performed the ex-situ XRD and FTIR to understand the structural changes before and after charging. XPS measurement shows the peak shifting before and after measurement in Lithium-based electrolytes. Further, we have fabricated double perovskite-based symmetric devices with gel electrolyte as a separator. The Cs3Bi2I9 device shows an areal energy density of ∼23 μWh/cm2, the highest among all halide perovskite-based supercapacitor devices reported to date. The flexible device on the S.S. substrate shows 79% and 82% capacitance retention up to 180° bending angle and 200 bending cycles, respectively.

Incorporating porous carbon materials into ionic liquid for high efficiency extraction of polycyclic aromatic hydrocarbons

Ionic liquid is an ideal candidate in the extraction of aromatic compounds. The design and construction of ionic liquids with high extraction efficiency and selectivity towards to the specific aromatics remain crucial question. In this paper, with the aid of orthogonal array experiment, the imidazolium-based ionic liquids with long alkyl chain on the cations were determined to possess high aromatics extraction efficiency. Furthermore, the Lewis acid anion was introduced into the ionic liquid to form 1-dodecyl-3-methylimidazolium ferric chloride ([C12mim][FeCl4]) and performed 62 % and 100 % extractant efficiency of naphthalene (NAP) and anthracene (ANT), respectively. Then the porous carbon materials (P1-1000) derived from hyper-crosslinked porous polymers (HCP) which possessed high BET surface area (1186 m2/g) was dispersed in [C12mim][FeCl4] to form porous ionic liquid. The single extraction efficiency of NAP improved from 62 % to 77 %. The great single extraction efficiency was attributed to the high porosity, additional adsorption sites provided by the Lewis acid anions and the hydrophobic long alkyl chain on the cations. After three times extraction, the concentration of NAP dropped down to 0. The porous ionic liquids also showed good recycle performance. The construction of porous ionic liquids provided an efficient approach for extraction of polycyclic aromatic hydrocarbons from aliphatic hydrocarbon.

Highly Porous Carbon Materials Prepared Through KOH‐Assisted CO2‐Activation of Carbonized Waste Tires for Removal of Cr(VI) and Cd(II) from Water

AbstractIn this study, waste tires (WTs) were carbonized under an N2 atmosphere. Subsequently, KOH/WTs‐char with KOH‐assisted CO2 activation was used to prepare activated carbon (AC) as a highly porous carbon material for the removal of Cr(VI) and Cd(II) from water. Various techniques such as elemental analysis, Fourier‐transform infrared spectroscopy, scanning electron microscopy, and N2 adsorption/desorption were employed to investigate the physical and chemical characteristics of the prepared carbons. The WTs‐char activated with KOH under CO2 exhibited a microstructure with a high BET surface area and pore volume of 1841 m2/g and 0.869 cm3/g, respectively, demonstrating excellent adsorbent performance. The maximum removal efficiencies of 99.91 % for Cd(II) and 99.81 % for Cr(VI) were achieved using AC2 carbon under the following conditions: pH 2 for Cr(VI) and pH 5 for Cd(II), contact time of 120 min, adsorbent dose of 0.4 g/100 mL, and temperature of 298 K. The adsorption kinetics followed the pseudo‐second‐order equation, and the equilibrium data fit well with the Redlich–Peterson isotherm equation. The positive values of ▵G indicated that the uptake process for both ions was nonspontaneous and nonfeasible over the temperature studied. Both ions showed negative values of ΔH and ΔS on carbon, suggesting exothermic adsorption and a decrease in disorder. Regeneration studies showed that NaOH was a better desorbing agent than HCl. Cr(VI) desorption resulted in over 90 % removal recovery by AC2 using 1.0 M NaOH even after the fifth cycle. However, the low activation energy indicated that the adsorption was favorable kinetically. Overall, this study demonstrated the effective preparation of highly porous carbon and its successful performance in removing Cr(VI) and Cd(II) ions.

Naphthenic acids removal using N-doped hemp fibers based mesoporous carbon from aqueous waste stream

There is a substantial need for removing the contaminants from aqueous waste stream using affordable, stable, and active adsorbents, such as heteroatom-doped carbonaceous materials. Heteroatom such as N-doped carbonaceous materials greatly improve the performance of carbon materials by enhancing their conductivity, basicity, oxidation stability, catalytic activity and adsorption capacity. In this study, hemp fibers (HFs) and N-aminoguanidine were utilized as carbon and nitrogen precursors to synthesize N-functionalized mesoporous carbon materials (N-HFCs) via simultaneous activation and carbonization with ZnCl2. Higher BET surface area with a distinctive mesoporous structure and the covalent bond between N and C was developed in the prepared carbon, making N-HFCs suitable for adsorbing naphthenic acids (2-naphthoic acid and benzoic acid) from aqueous waste streams. Developed covalent bond helps to prevent the leaching of carbonaceous materials during adsorption study. The results showed that N-HFC-2 (ZnCl2: N-HFs ratio = 2:1) exhibited a higher removal efficiency of naphthenic acids (2-naphthoic acid and benzoic acid) compared to nonfunctionalized porous carbon (HFC). Adsorption of 2-naphthoic acid and benzoic acid on the adsorbents followed the typical monolayer type of Langmuir adsorption model. The maximum adsorption capacity of HFC after 48 h was evaluated as 70 and 27 mg/g for 2-naphthoic acid and benzoic acid. Likewise, the maximum adsorption capacity of N-HFC-2 for 2-naphthoic acid and benzoic acid was found to be 71 and 33 mg/g. In the adsorption kinetic experiment, adsorption of 2-naphthoic acid and benzoic acid reached equilibrium within 1 h using both the adsorbents (N-HFC-2 and HFC). Adsorption kinetics were analyzed using pseudo-first-order and pseudo-second-order kinetic models and were found to follow a pseudo-second-order kinetic model. Although changing pH from 4.4 to 8.5 did not have any significant effect on the removal efficiency of 2-napthoic acid using HFC and N-HFC-2, the removal efficiency of benzoic acid was decreased from 94 to 60 % using HFC and increased from 98 to 100 % using N-HFC-2. Comparative evaluations demonstrated that the mesoporous carbonaceous materials derived from HFs are an attractive adsorbent for removal of such contaminants from contaminated aqueous streams.

Synthesis of multifunctional mesoporous geopolymer under hydrothermal curing: High mechanical resistance and efficient removal of methylene blue from aqueous medium

This study created green multifunctional geopolymeric sorbent material with strong cationic dye adsorption capacity and superior mechanical strength to broaden lead sludge (LS)-based geopolymer applications. In this study, two geopolymeric sorbents (Go and G) were fabricated using slag blended with 0 and 50 wt% LS, respectively and activated with 6 wt% NaOH. The Go and G specimens were normally cured for up to 28 days, while G specimens were hydrothermally cured at different steam-pressures to modify/improve histological characteristics as well as mechanical resistance. The selected sorbents were characterized via XRD, FTIR, TGA/DTG, XPS, N2-adsorption/desorption and SEM/EDX techniques. G/5 bar′s high strength and adsorption capacity may be due to the production of CSH, CAH, CASH, and NASH, which formed a fine mesoporous zeolitic structure with the highest BET-surface area (64.55 m2/g) and lowest BJH-maximum pore diameter (9.68 nm). The maximum MB adsorption capacity of the synthesized adsorbent was 230.4 mg/g.

Enhanced benzene vapor adsorption through microwave-assisted fabrication of activated carbon from peanut shells using ZnCl2 as an activating agent

Herein, microwave-assisted activated carbon (MW-AC) was fabricated from peanut shells using a ZnCl2 activator and utilized for the first time to eliminate benzene vapor as a volatile organic compound (VOC). During the MW-AC production process, which involved two steps—microwave treatment and muffle furnace heating—we investigated the effects of various factors and achieved the highest iodine number of 1250 mg/g. This was achieved under optimal operating conditions, which included a 100% impregnation ratio, CO2 as the gas in the microwave environment, a microwave power set at 500 W, a microwave duration of 10 min, an activation temperature of 500 °C and an activation time of 45 min. The structural and morphological properties of the optimized MW-AC were assessed through SEM, FTIR, and BET analysis. The dynamic adsorption process of benzene on the optimized MW-AC adsorbent, which has a significant BET surface area of 1204.90 m2/g, was designed using the Box-Behnken approach within the response surface methodology. Under optimal experimental conditions, including a contact duration of 80 min, an inlet concentration of 18 ppm, and a temperature of 26 °C, the maximum adsorption capacity reached was 568.34 mg/g. The experimental data are better described by the pseudo-second-order kinetic model, while it is concluded that the equilibrium data are better described by the Langmuir isotherm model. MW-AC exhibited a reuse efficiency of 86.54% for benzene vapor after five consecutive recycling processes. The motivation of the study highlights the high adsorption capacity and superior reuse efficiency of MW-AC adsorbent with high BET surface area against benzene pollutant. According to our results, the developed MW-AC presents itself as a promising adsorbent candidate for the treatment of VOCs in various industrial applications.

Room temperature hybridization of amide-linked COF (RT-COF) and Na-mordenite zeolite (MOR) as a potential adsorbent in three-medium iodine capture

Generated volatile radionuclides within the nuclear fission process, namely, iodine considered a threat to human safety and cause environmental pollution. Herein, we studied the crystallization of a stable nanoporous hybrid containing a covalent organic framework (COF) and Na-mordenite zeolite, operated as an adsorbent platform for efficient volatile iodine capture towards vapor, organic and aqueous mediums. The room-temperature synthesized hybrid, prepared by ease-operated rapid reaction, possesses a high BET surface area of over 140 m2 g−1, good both crystallinity and thermal stability with high capture of iodine (7.2 g g−1, 78.54 %, and 83.40 % in vapor, aqueous and organic phases, respectively), which was significantly higher than individual hybrid ingredients (Na-MOR and RT-COF). The nanoporous hybrid represented the ability to be recycled three times while maintaining a high uptake capacity. We believe that the applied combination of COF with zeolite will pave the way for the advent of novel impressive adsorbent materials for radioiodine during nuclear waste disposal.

The key role played by mesoporous alumina as binder for obtaining ultra-hard CaO based pellets for thermochemical heat storage leveraging the CaO/CaCO3 cycle

The synthesis of CaO-based pellets with high energy storage and suitable mechanical resistance after prolonged cycling is pivotal for the successful implementation of the Calcium looping (CaL) technology for energy storage in CSP plants. In this work, CaO-based spherical pellets (CAA) were prepared made up of 60 wt % Ca(OH)2 and varying ratios (0–40 wt %) of commercial γ-Al2O3 and mesoporous γ-Al2O3 (m-Al2O3). They were tested in TG in several CO2 carbonation/decarbonation cycles (15 and 50 for selected pellets) and their respective average crushing strengths measured. After 15 cycles, the optimum pellet CAA 20-20 (60 wt % Ca(OH)2/20 wt % γ-Al2O3/20 wt % m-Al2O3) exhibits a remarkable energy storage density of 1030 kJ/kg with a superb crushing strength of ∼29 N. This was ascribed to the enhanced formation of the calcium aluminate mayenite (Ca12Al14O33), since the high BET surface area (384 m2 g−1) of mesoporous γ-Al2O3 promotes the interaction with calcium oxide. Additionally, CAA 20-20 showed meaningful porosity that favored CO2 mass transport. Interestingly, after 50 cycles, the optimum CAA 20-20 pellet maintained a high carbonation yield (0.46), representing an 84 % of the initial value and corresponding to an energy storage density of ∼873 kJ/kg. Additionally, the optimum CAA 20-20 pellet was coated with an external layer of Al-MCM-41 silica that augmented its crushing strength up to 37 N, with a concurrent slight abatement in the carbonation yield and energy storage density after 50 cycles (0.43 and ∼824 kJ/kg). Consequently, both uncoated and coated CAA 20-20 pellet are promising for the successful implementation of CaL in CSP plants.

Graphene-containing biocarbon from burlap waste: Property comparison with commercial grade graphene nanoplatelets

In this paper, we report a method for synthesizing high-yield graphene-containing biocarbon from burlap waste through a simple two-step carbonization process. The first step involves feedstock carbonization at 600 °C, followed by ball milling and then graphitization at 1200 °C using KOH. A comparative analysis between the obtained bio-graphene and commercial graphene revealed superior graphene properties of the burlap-based graphene. Notably, this bio-based graphene exhibited exceptional characteristics such as a very high BET surface area in the range of 1021 m²/g, low defect-to-graphene ratio of 0.12 in the Raman spectra, and an overall yield of 19% wt. These findings highlight the potential of burlap waste as a sustainable precursor for high-quality graphene synthesis and its potential for various applications.

The flexible DADM-based covalent organic frameworks constructed by flexible knots and 4,4′-diaminodiphenylmethane as a linker for fluorescence sensing nitrophenol and adsorping iodine

Enrichment of nitro-aromatic compounds (NACs) and radioactive iodine seriously threatens the health of humans, therefore, trace detection of NACs and the efficient capture and storage of radioactive iodine have attracted a great deal of attention in recent years. Herein, we present two highly efficient flexible DADM-based covalent organic frameworks (DADM-based COFs) for the fluorescence sensing of o-nitrophenol (o-NP) and p-nitrophenol (p-NP) and reversible iodine capture, namely TDADM and HDADM. The resulting TDADM and HDADM have excellent thermal and chemical stability, some crystallinity and high BET surface areas of 1035 and 958 m2 g−1, respectively. For fluorescence sensing, TDADM and HDADM show high sensitivity to o-NP and p-NP with quenching constants (Ksv) of 6.77 × 103 and 3.39 × 104 L mol−1, respectively. The fluorescence quenching of TDADM is caused by the action of photo-induced electron transfer (PET) processes. The fluorescence quenching of HDADM is caused by the co-action of PET and resonance energy transfer (RET) processes. For iodine capture, TDADM and HDADM exhibit high iodine capture capacities, which are severally up to 4.08 and 5.32 g g−1. Such high iodine adsorption amounts are caused by the electron transfer of the electron-rich flexible DADM-based COFs to the electron-deficient I2 into the polyiodide anion complexes.

Encapsulating Sulfur into a Gel-Derived Nitrogen-Doped Mesoporous and Microporous Carbon Sponge for High-Performance Lithium-Sulfur Batteries.

The practical application of Li-S batteries (LSBs) has long been impeded by the inefficient utilization of sulfur and slow kinetics. Utilizing conductive carbonaceous frameworks as a host scaffold presents an efficient and cost-effective approach to enhance sulfur utilization for redox reactions in LSBs. However, the interaction of pure carbon materials with lithium polysulfide intermediates (LiPSs) is limited to weak van der Waals forces. Hence, the development of an economical method for synthesizing heteroatom-doped carbon materials for sulfur fixation is of paramount importance. In this study, we introduce a hierarchical porous nitrogen-doped carbon sponge (NPCS) with an exceptionally high BET surface area of 3182.2 m2 g-1, achieved through a facile template-assisted polymerization method. The incorporation of inorganic salts, free radical polymerization, and deuteric freeze-drying techniques facilitates the formation of hierarchical pores within the NPCS. After sulfur fixation, the resulting S/NPCS electrode demonstrates remarkable electrochemical performance in LSBs. Specifically, it achieves an 80% sulfur utilization rate, maintains a high reversible specific capacity of 400 mA h g-1 even after 600 cycles at a demanding current density of 5.0 A g-1, and exhibits superior rate capability. It is believed that this work will inspire the rational design of cost-effective carbon-based electrodes for high-performance LSBs.

In-situ crosslinking of a novel conjugated dialkynyl-based polyimide for high performance carbon molecular sieve membrane

High-performance and reliable membranes for efficient gas separation and their design strategies are key points for membrane-based carbon capture. Here, we reported a high-performance carbon membrane design protocol from a microporous, highly rigid polyimide precursor (6FBD1-CR), which was produced by in-situ crosslinking a polyimide (6FBD1) containing conjugated dialkynyl group at 300 °C. The possible crosslinking mechanisms are the [2+2+2] trimerization of three ethynyl groups to form a benzene ring and the Diels-Alder reaction between the ethynyl bond and phenylacetylene to generate the fused naphthalene ring. After crosslinking, the membrane shows a ∼ 8-fold improved microporosity (37.1–298 m2 g−1). When pyrolyzed at 550 °C, the resulting 6FBD1-CMS demonstrates very high pure- and mixed-gas separation performance. E.g., the CO2 permeability reaches 7661 Barrer and CO2/CH4 selectivity of 44, additionally, even at the CO2/CH4 mixed-gas pressure of 30 bar, the PCO2 can still reach 4920 Barrer combined with a αCO2/CH4 of 28, which is well above the latest CO2/CH4 mixed-gas Upper Bound line. We consider this is due to the acetylene crosslinking induced a very stable microporous structure composed of rigid fused rings that alleviate the micropore collapse during the carbonization process, and thus, resulting in a relatively higher BET surface area, larger d-spacing, relatively higher concentration of continuous disordered phase (higher sp3/sp2) and small activation energy (Ep) for gas transport than the CMSM derived from polyimide without pre-crosslinking. This finding provides new opportunity for the structural design of high-performance CMSMs.

Development of Dual N, S‐Heteroatom Doped Hollow Carbon Spheres as an Alternative Electrocatalyst for Oxygen Reduction Reaction in Alkaline Medium

AbstractHollow heteroatom‐doped mesoporous carbons were found to be an efficient non‐noble metal catalyst to enhance the oxygen reduction reaction (ORR) in fuel cells. Here, we use dopamine hydrochloride (DHC) and dibenzyl disulfide (DBS) as the nitrogen and sulfur precursors to infiltrate N and S into the HCS in a single‐step process. Dibenzyl disulfide is less explored in literature as a sulfur dopant. Due to its high sulfur content and high boiling point, dibenzyl disulfide acts as an excellent sulfur dopant and can withstand the carbonization process. Among them, NSMHCS‐0.2 obtained by adding 0.2 g of dibenzyl disulfide at 31 h intervals to the polydopamine (PDA) loaded silica leads to the ideal N, S dual hetero‐atom doping in NSMHCS. Notably, it has a high shell thickness (45 nm), high BET surface area (637 m2 g−1), high pyridinic nitrogen (13.54 %), and thiophene sulfur (89.8 %) concentration. Such property tuning paved the way to reach a high positive onset potential (0.86 V vs RHE) and a limiting current density of 3.64 mA cm−2 at 0.4 V vs RHE. Additionally, NSMHCS‐0.2 has shown superior methanol tolerance and strong electrochemical stability when compared to Pt/C 20 %.

A bifunctional 3D porous MOF with potential for fluorescence sensing of picric acid and natural gas purification

A pillared-layer fluorescence metal-organic framework [Zn2(TCPP)(BPE), GXZ-1] has been synthesized by using the AIE ligand 2,3,5,6-tetrakis(4-carboxyphenyl) pyrazine (TCPP) and 1,2-Bis(4-pyridyl) ethylene (BPE). The GXZ-1 exhibited remarkable stability in both air and various solvents. Furthermore, fluorescence experiments demonstrated its potential as a fluorescence probe for the sensitive detection of picric acid (PA). Additionally, the activated GXZ-1 exhibited permanent porosity with a high BET surface area of 210.59 m2 g−1 and a narrow pore size distribution of 0.6 nm. These properties enable GXZ-1 ideally suitable for gas separation applications. Gas adsorption experiments revealed promising CO2/CH4 separation properties, with an IAST adsorption selectivity of 8.37 and 5.39 for equimolar CO2/CH4 gas mixtures at 273/298 K and 1 atm, respectively. In addition, GXZ-1 displayed outstanding chemical and thermal stability, further enhancing its potential for practical applications.

Hydrothermally synthesized MXene Ti3C2/Zn2SnO4 based nanocomposite for H2S sensing at room temperature

Hydrogen sulfide (H2S) gas sensors with high response and minimum limit of detection at room temperature are of great importance to ensure the safety of humans and the environment. A series of samples such as MXene Ti3C2, Ti3AlC2, WS2, MoSe2/Zn2SnO4 and spherical Zn2SnO4 nanoparticles were synthesized via hydrothermal method in this paper. Different characterizations were performed on these samples to check crystal structures, morphologies, chemical states, etc. And gas sensing properties were also performed and analyzed deeply. A series of sensor sheets were fabricated via the spin coating method based on synthesized samples for gas sensing properties. MXene Ti3C2/Zn2SnO4-5 based gas sensor detected the highest response (110) towards 8 ppm H2S with excellent selectivity, the minimum limit of detection (0.01 ppm), mediate long-term stability and good reproducibility compared with other fabricated sensors at room temperature. Also, the sensor response was increased with the increase of H2S concentration. Experimental results showed that the highest response of Ti3C2/Zn2SnO4-5 based gas sensor was accredited to heterojunction, higher BET surface area, and increased oxygen species. The simple way synthesized nanocomposite and fabricated sensors throw a novel idea for tracing H2S at the lowest concentration to prevent different diseases.

Regioisomeric Spirobifluorene CANAL Ladder Polymers and Their Gas Separation Performance.

We synthesized and characterized two isomeric microporous hydrocarbon ladder polymers from catalytic arene norbornene annulation (CANAL) of regioisomeric bis-norbornene fused spirobifluorenes, where the ladder chains are connected either through the same fluorene unit or across two different fluorene units in spirobifluorene. This pair of isomeric polymers was used to investigate the effect of ladder macromolecular structures on the microporosity and transport properties. Both polymers form mechanically intact films with thermal stability up to 480 °C and relatively high BET surface areas. The polymer formed from 2,7-dibromospirobifluorene showed higher BET surface area and higher gas permeability than the polymer from 2,2'-dibromospirobifluorene despite similar intersegmental spacing as indicated by X-ray scattering. The aging behavior for both polymers followed the same trend as the previously reported CANAL-fluorene polymers, with dramatically increased permselectivities over time, resulting in gas separation performance above the 2008 upper bounds for H2/CH4 and O2/N2.

Magnetically separable Co0.6Fe2.4O4/MIL-101-NH2 adsorbent for Congo red efficient removal.

The development of effective and practical adsorbents for eliminating pollutants still remains a significant challenge. Herein, we synthesized a novel magnetically separable composite, Co0.6Fe2.4O4/MIL-101-NH2, through the in-situ growth of MIL-101-NH2 on magnetic nanoparticles, designed specifically for the removal of Congo red (CR) from aqueous solutions. MIL-101-NH2 possessed high BET surface area (240.485 m2•g-1) and facile magnetic separation function and can be swiftly separated (within 30s) through an external magnetic field post-adsorption. The investigation systematically explored the influence of crucial parameters, including adsorbent dosage, pH, adsorption duration, temperature, and the presence of interfering ions, on CR adsorption performance. Findings indicate that CR adsorption adheres to the pseudo-second-order (PSO) kinetic model and the Langmuir isotherm model. Thermodynamic analysis reveals the spontaneity, endothermic nature, and orderly progression of the adsorption process. Remarkably, the adsorbent with 0.1g•L-1 boasts an impressive maximum adsorption capacity of 1756.19mg•g-1 for CR at 298.15K, establishing its competitive advantage. The reuse of the adsorbent over 5 cycles remains 78% of the initial adsorption. The CR adsorption mechanisms were elucidated, emphasizing the roles of π-π interactions, electrostatic forces, hydrogen bonding, and metal coordination. Comparison with other dyes, such as methylene blue (MB) and methyl orange (MO), and exploration of adsorption performance in binary dye systems, demonstrates the superior capacity and selectivity of this adsorbent for CR. In conclusion, our magnetically separable metal-organic framework (MOF)based composite presents a versatile and effective solution for CR removal, with promising applications in water treatment and environmental remediation.

Copper Dispersed Covalent Organic Framework for Azide-Alkyne Cycloaddition and Fast Synthesis of Rufinamide in Water.

A crystalline porous bipyridine-based Bpy-COF with a high BET surface area (1864m2g-1) and uniform mesopore (4.0nm) is successfully synthesized from 1,3,5-tris-(4'-formyl-biphenyl-4-yl)triazine and 5,5'-diamino-2,2'-bipyridine via a solvothermal method. After Cu(I)-loading, the resultant Cu(I)-Bpy-COF remained the ordered porous structure with evenly distributed Cu(I) ions at a single-atom level. Using Cu(I)-Bpy-COF as a heterogeneous catalyst, high conversions for cycloaddition reactions are achieved within a short time (40min) at 25°C in water medium. Moreover, Cu(I)-Bpy-COF proves to be applicable for aromatic and aliphatic azides and alkynes bearing various substituents such as ester, hydroxyl, amido, pyridyl, thienyl, bulky triphenylamine, fluorine, and trifluoromethyl groups. The high conversions remain almost constant after five cycles. Additionally, the antiepileptic drug (rufinamide) is successfully prepared by a simple one-step reaction using Cu(I)-Bpy-COF, proving its practical feasibility for pharmaceutical synthesis.

A sustainable approach to combat industrial air pollution using commercially available and engineered gas-phase adsorbents

The occurrence of benzene, toluene, ethylbenzene, and xylene (BTEX) in the environment has human health and ecological consequences; hence, it is essential to remediate the gas-phase industrial plume before its release. A laboratory-scale experimental apparatus was designed to investigate single-component gas-phase adsorption of BTEX compounds on commercially available granular activated carbon (CGAC) and laboratory-developed Mesquite-derived granular activated carbon (MDAC). The physical properties of CGAC and MDAC show that these adsorbents have a high N2 BET surface area, with CGAC exhibiting microporosity features. The single-component adsorption of BTEX was modeled by considering the transport of BTEX by axial dispersion, convective transport, and accumulation in the adsorbent bed at isothermal conditions. A linear driving force model was used to examine the mass transfer process. The experimental breakthrough curves showed good agreement with the modeled breakthrough curves. The modeling parameters demonstrated the dominance of intraparticle diffusion with a negligible external diffusion of BTEX onto CGAC and MDAC. The analysis of experimental data validated the modeled dynamic behavior of BTEX adsorption onto CGAC and MDAC. Overall, BTEX compounds followed Langmuir isotherms for both adsorbents, with intra-particle diffusion as a dominant gas phase adsorption mechanism.

High surface area of carbonaceous Cr2GaC composite microspheres synthesized by sol–gel chemistry

Carbonaceous Cr2GaC microspheres are synthesized by means of sol–gel chemistry and exhibit high BET surface area after pyrolysis.