Low Surface Area Research Articles

Textile dyes removing from the wastewater by green synthesized Cu-doped ZnO photocatalysts under the simulated sunlight illumination

Herein, Cu-doped ZnO photocatalysts were prepared via green synthesis method with utilization of Cannabis Sativa leaves. The catalytic activity was evaluated through the degradation of methylene blue (MB) and rhodamine B (RhB) under the simulated sunlight illumination. XRD, FESEM, EDAX, FTIR, BET-BJH and DRS were used for characterizations of Cu-doped ZnO. The results showed that, 3 wt % Cu-doped ZnO (CuZn3) displayed the excellent characterizations such as uniform dispersion, lower energy bandgap, smaller average particle size and greater surface area. For the photocatalysts with higher Cu loading (more than 3 wt %), non-uniform dispersion with larger particles, lower specific surface area and higher energy bandgap were found. The average particle size and energy bandgap for CuZn3 were 37.7 nm and 2.9 eV, respectively. Due to the superior properties, CuZn3 presented the highest amount of dyes degradations. After 180 min test, MB and RhB degradations by CuZn3 were 92.1 and 94.2 %, respectively. Moreover, it was found that optimum amount of CuZn3 was 100 ppm. Furthermore, applying of various scavengers revealed that hydroxyl radicals, superoxide radicals, and photo-generated electrons were the primary forms of radicals involved in dyes degradation using Cu-doped ZnO photocatalysts.

Dehydration of Alcohols to Olefins Catalyzed by ZrAPSO-34 Molecular Sieve

The lower olefins (Ethylene, propylene, and butylene) are considered the key to the polymeric and petrochemical industries. Dehydration of alcohols to produce light olefins (Methanol-to-olefins reaction) over SAPO-34 molecular sieve has attractedintoigh attention. Modified SAPO-34 zeolite catalyst with Zr metal was successfully prepared under microwave irradiation using morpholine as a structure direct agent. The microwave energy power used was 800 w and the crystallization time was 200 min. The catalyst sample was characterized by XRD, SEM, EDX, BET, FTIR, and TGA analysis. XRD analysis exhibited a typical chabazite structure with high crystallinity. The analysis showed macrocrystalline particles with moderate distribution of silica in the framework structure and a low surface area of 77 m2/g. The vibration peaks of the prepared catalyst showed agreement with the SAPO-34 CHA structure. Catalyst performance towards methanol-to-olefins conversion was performed in a trickle bed reactor with temperatures of 350, 400, 450, and 500 oC at a weight hourly space velocity of 7.7 h-1. The results also reveal at a temperature of 400 oC , that the best olefins selectivity was obtained, reaching 70%, with a longer lifetime of 500 min. methanol conversion was almost 100% at all reaction temperatures. In addition, the effect of methanol concentration was investigated and the results showed that increasing of water content plays a role in increasing catalyst lifetime and preventing coke depositions in pores.

Laser Additive Manufacturing of Three-Dimensional Ti/TiN Nanotube Arrays with Hierarchical Pore Structures and Promoted Supercapacitor Performances.

Titanium-based composites hold great promise in versatile functional application fields, including supercapacitors. However, conventional subtractive methods for preparing complex-shaped titanium-based composites generally suffer from several significant shortcomings, including low efficiency, strictly simple geometry, low specific surface area, and poor electrochemical performance of the products. Herein, three-dimensional composites of Ti/TiN nanotube arrays with hierarchically porous structures were prepared using the additive manufacturing method of selective laser melting combined with anodic oxidation and nitridation. The resultant Ti/TiN nanotube array composites exhibit good electrical conductivity, ultrahigh specific surface areas, and outstanding supercapacitor performances featuring the unique combination of a large specific capacitance of 134.4 mF/cm2 and a high power density of 4.1 mW/cm2, which was remarkably superior to that of their counterparts. This work is anticipated to provide new insights into the facile and efficient preparation of high-performance structural and functional devices with arbitrarily complex geometries and good overall performances.

Artificial neural network modelling and experimental investigations of malachite green adsorption on novel carboxymethyl cellulose/β-cyclodextrin/nickel cobaltite composite

This study presents a novel polymer nanocomposite based on carboxymethyl cellulose and β-cyclodextrin crosslinked with succinic acid (CMC-SA-β-CD) containing nickel cobaltite (NCO) nano-reinforcement. Various analytical techniques have been employed to investigate the structural, thermal, and morphological features of the resulting nanocomposite. The CMC-SA-β-CD/NCO nanocomposite has been utilized as an adsorbent for the removal of bisphenol-A (BPA, R% <40 %), malachite green (MG, R% > 75 %)), and Congo red (CR, no adsorption) from the synthetic wastewater. The study systematically explored the impact of various parameters on the adsorption process, and the interactions between MG and CMC-SA-β-CD/NCO were discussed. The adsorption data were fitted to different models to elucidate the kinetics and thermodynamics of the adsorption process. An artificial neural network (ANN) analysis was employed to train the experimental dataset for predicting adsorption outcomes. Despite a low BET surface area (0.798 m2 g−1), CMC-SA-β-CD/NCO was found to exhibit high MG adsorption capacity. CMC-SA-β-CD/NCO exhibited better MG adsorption performance at pH 5.5, 40 mg L−1 MG dye concentration, 170 min equilibrium time, 20 mg CMC-SA-β-CD/NCO dose with more than 90 % removal efficiency. Moreover, the thermodynamic studies suggest that the adsorption of MG was exothermic with ΔH° value −9.93 ± 0.76 kJ mol−1. The isotherm studies revealed that the Langmuir model was the best model to describe the adsorption of MG on CMC-SA-β-CD/NCO indicating monolayer surface coverage with Langmuir adsorption capacity of 182 ± 4 mg g−1. The energy of adsorption (11.4 ± 0.8 kJ mol−1) indicated chemisorption of MG on the composite surface. The kinetics studies revealed that the pseudo-first-order model best described the adsorption kinetics with qe = 86.7 ± 2.9 mg g−1. A good removal efficiency (>70 %) was retained after five regeneration reuse cycles. The ANN-trained data showed good linearity between predicted and actual data for the adsorption capacity (R-value>0.99), indicating the reliability of the prediction model. The developed nanocomposite, composed predominantly of biodegradable material, is facile to synthesize and exhibited excellent monolayer adsorption of MG providing a new sustainable adsorbent for selective MG removal.

Multi-metric predictors of radiofrequency-treated trigeminal neuralgias.

Evaluation of neurovascular compression-related trigeminal neuralgia (NVC-TN) and its resolution through microvascular decompression are demonstrable by MRI and intraoperatively [Leal et al. (Atrophic changes in the trigeminal nerves of patients with trigeminal neuralgia due to neurovascular compression and their association with the severity of compression and clinical outcomes: Clinical article. J Neurosurg. 2014;120(6):1484-1495)]. Non-NVC-TNs treated by radiofrequency (RF) lack such detectable features. Multimodal integration of pre-surgical diffusion tensor imaging (DTI) and volumetry (VOL) with intraoperative neurophysiology (ION) could improve understanding and performance of RF among non-NVC-TN. We hypothesized that DTI disturbances' localization (central relay versus peripherally) rather than their values bares the most significant predictive value upon outcome and that ION could quantitatively both localize and assist RF of affected branches. The first pre-surgical step evaluated the differences between affected and non-affected sides (by DTI and VOL). Four TN's segments were studied, from peripheral to central relay: Meckel's cave-trigeminal ganglion (MC-TGN), cisternal portion, root entry zone (REZ) and spinal tract [Lin et al. (Flatness of the Meckel cave may cause primary trigeminal neuralgia: A radiomics-based study. J Headache Pain. 2021;22(1):104)]. In the second intraoperative step, we used both ION and patient's testimonies to confirm the localization of the affected branch, evolving hypoesthesia, pain reduction and monitoring of adverse effects [Sindou (Neurophysiological navigation in the trigeminal nerve: Use of masticatory responses and facial motor responses evoked by electrical stimulation of the trigeminal rootlets for RF-thermorhizotomy guidance. Stereotact Funct Neurosurg. 1999;73(1-4):117-121); Sindou and Tatli (Traitement de la névralgie trigéminale par thermorhizotomie. Neurochirurgie. 2009;55(2):203-210)]. Last and postoperatively, each data set's features and correlation with short-term (3 months) and long-term outcomes (23.5 ± 6.7 months) were independently analysed and blind to each other. Finally, we designed a multimodal predictive model. Sixteen non-NVC-TN patients (mean 53.6 ± SD years old) with mean duration of 6.56 ± 4.1 years (75% right TN; 43.8% V3) were included. After 23.5 ± 6.7 months, 14/16 were good responders. Age, gender, TN duration and side/branch did not correlate with outcomes. Affected sides showed significant DTI disturbances in both peripheral (MC-TGNs) and central-relay (REZ) segments. However, worse outcome correlated only with REZ-located DTI disturbances (P = 0.04; r = 0.53). Concerning volumetry, affected MC-TGNs were abnormally flatter: lower volumes and surface area correlated with worse outcomes (both P = 0.033; r = 0.55 and 0.77, respectively). Intraoperatively, ION could not differ the affected from non-affected branch. However, the magnitude of ION's amplitude reduction (ION-Δ-Amplitude) had the most significant correlation with outcomes (r = 0.86; P < 0.00006). It was higher among responders [68.4% (50-82%)], and a <40% reduction characterized non-responders [36.7% (0-40%)]. Multiple regression showed that ION-Δ-Amplitude, centrally located only REZ DTI integrity and MC-TGN flatness explain 82.2% of the variance of post-RF visual analogue score. Integration of pre-surgical DTI-VOL with ION-Δ-Amplitude suggests a multi-metric predictive model of post-RF outcome in non-NVC-TN. In multiple regression, central-relay REZ DTI disturbances and insufficiently reduced excitability (<40%) predicted worse outcome. Quantitative fine-tuned ION tools should be sought for peri-operative evaluation of the affected branches.

Understanding adsorption selectivity in zirconium-pillared clays for biogas upgradation: the role of metal/clay ratio.

Biogas, as a sustainable energy source, encounters challenges in practical applications due to impurities, notably carbon dioxide (CO2), and nitrogen (N2). This study investigates the effect of metal/clay ratio on the adsorption selectivity of porous zirconium-pillared clay adsorbents for biogas upgradation. Comprehensive analyses including nitrogen adsorption/desorption, X-ray diffraction (XRD), and Fourier-transform infrared spectroscopy (FTIR) were conducted to evaluate the physicochemical properties. Adsorption properties for Zr-pillared clays for biogas components such as CO2, CH4, and N2, at 25 °C under different pressures were investigated. The ideal adsorbed solution theory (IAST) was employed to assess selectivity for three binary gas mixtures (CO2/CH4, CO2/N2, and CH4/N2). Results revealed the substantial impact of Zr/Clay ratio on both adsorption capacity and selectivity of the prepared materials. For instance, the maximum adsorption capacity of gases varies as ZrPILC-4 > ZrPILC-2 > ZrPILC-8 > ZrPILC-1, whereas the adsorption selectivity for CO2/CH4 separation (at 1000kPa) varies as ZrPILC-1 > ZrPILC-2 > ZrPILC-8 > ZrPILC-4. Interestingly, the ZrPILC-8 with maximum surface area (147 m2∙g-1) did not show maximum adsorption capacity for all the three gases, which was attributed to its lower pore volume, and basal spacing, as compared to ZrPILC-4. Amongst all the pillared samples, the ZrPILC-1 exhibited highest selectivity for all binary mixtures (at 1000kPa), signifies increased nonspecific interactions due to its lower surface area. Its separation performance, particularly for CO2/CH4 mixture exceeded that of the parent clay by 1.5 times. A significant increase in the working capacity of the prepared samples underscores the efficacy of these pillared materials in separating biogas components. This study provides valuable insights into effects of Zr/clay ratio for developing robust pillared adsorbents, contributing to the advancement of sustainable biomethane production.

Ionic copolymer-modified hexagonal carbon nitride tube as a high-performance catalyst for regioselective synthesis of hexahydroquinoline frameworks

The conventional structure of carbon nitride materials presents limitations, especially in the catalysis field, attributed to a restricted number of active sites and a low surface area. To address these challenges, we developed a unique design for a mesoporous carbon nitride tube (CNT), which was constructed by incorporating the ionic imidazole-epichlorohydrin copolymer ([IMEP][Cl]) as a template in the fabrication process. The self-assembly behavior of [IMEP][Cl] influences the formation of the melamine-cyanuric acid aggregate (as precursors) through electrostatic forces and polarity, potentially resulting in the creation of a thin-wall CNT with unique pore morphology. Synthesized three-dimensional hollow CNT demonstrated key factors of a high-performance catalyst in terms of high thermal stability (up to 550 °C), good specific surface area (108 m²/g), and significant recoverability (seven runs without a significant decrease in reaction yield). The CNT architecture was employed as a heterogeneous catalyst, and its catalytic efficiency was investigated in the regioselective synthesis of hexahydroquinoline ring systems. Based on the obtained results, CNT shows super-fast synthesis (5 min) of different pharmaceutical quinoline frameworks with exceptional yields (94–98 %) under ultrasound agitations. For the first time, an effective synthesis method is introduced for constructing hollow carbon nitride tubes, utilizing an ionic polymer (produced via chemical crosslinking rather than radical chain polymerization) as a template. This work offers a new viewpoint on improving the catalytic capability of traditional graphitic carbon nitrides through the utilization of ionic copolymers, presenting potential advancements for various technological applications.

Tea polyphenol reinforced polyacrylamide hydrogel as a regenerative adsorbent for low-concentration methylene blue

To remove the low-concentration methylene blue (MB) residues from liquid waste, we attempt to fabricate a hydrogel with good reusability and good removal efficiency. In this work, polyacrylamide (PAAm) hydrogel initially synthesized through polymerization and subsequently soaked in tea polyphenol (TP) aqueous solution to yield PAAm/TP hydrogels. The hydrogels were detected by Fourier transform infrared spectrometer, scanning electronic microscope, zeta electric potential instrument, full-automation surface area and porosity instrument, swelling degree, and universal testing machine. The results confirmed the successful preparation of PAAm/TP hydrogels with mesoporous structure. Compared to pure PAAm hydrogel, TP-reinforced PAAm hydrogel exhibited good mechanical properties and low swelling degree. Furthermore, PAAm/TP hydrogels were employed as an adsorbent for low-concentration MB owing to low specific surface area and mesoporosity. The effects of adsorption time, TP concentration, hydrogel level, starting MB level, pH value, and inorganic salts on MB adsorption were researched. PAAm/TP hydrogels had higher adsorption efficiency for low-concentration MB than pure PAAm hydrogel. The kinetic data of the PAAm/TP hydrogel coincided with the quasi-second-order model (R2 = 0.9997), and the adsorption rate was mainly governed by internal diffusion. The adsorption process highly followed the Freundlich isotherm model (R2 = 0.9755). Furthermore, the hydrogel demonstrated stability and excellent recyclability. Notably, the removal efficiency remained above 50 % even after five consecutive adsorption-desorption cycles. The mechanism analysis manifested that the MB adsorption was stimulated by electrostatic attraction, hydrogen bonding, and π-π stacking interreactions. Hence, the prepared PAAm/TP hydrogels brought a green and effective method for removing low-concentration MB from wastewater.

Extended Plateau Capacity of Hard Carbon Anode for High Energy Lithium-Ion Batteries.

Hard carbon materials have shown promising potential for sodium-ion storage due to accommodating larger sodium ions. However, as for lithium-ion storage, the challenge lies in tuning the high lithiation plateau capacities, which impacts the overall energy density. Here, hard carbon microspheres (HCM) are prepared by tailoring the cross-linked polysaccharide, establishing a comprehensive methodology to obtain high-performance lithium-ion batteries (LIBs) with long plateau capacities. The "adsorption-intercalation mechanism" for lithium storage is revealed combining in situ Raman characterization and ex situ nuclear magnetic resonance spectroscopy. The optimized HCM possesses reduced defect content, enriched graphitic microcrystalline, and low specific surface area, which is beneficial for fast lithium storage. Therefore, HCM demonstrates a high reversible capacity of 537mAhg-1 with a significant low-voltage plateau capacity ratio of 55%, high initial Coulombic efficiency, and outstanding rate performance (152mAhg-1 at 10Ag-1). Moreover, the full cell (HCM||LiCoO2) delivers outstanding fast-charging capability (4min charge to 80% at 10C) and impressive energy density of 393Whkg-1. Additionally, 80% reversible capacity can be delivered under -40°C with competitive cycling stability. This work provides in-depth insights into the rational design of hard carbon structures with extended low-voltage plateau capacity for high energy LIBs.

Enhanced acetaminophen photodegradation under UV using anatase–rutile TiO2 phase heterojunction – Z-scheme mechanism and factors affecting efficiency

In this work, the commercial Hombikat UV-100 anatase (AH) was calcined at 1000 °C for 4 h to obtain a rutile phase grown on anatase (AR), proven by X-ray diffraction pattern. The dry powder of AH and AR were physically mixed to form AH + AR samples in different ratios. Although the characterization of AR revealed that it had microstructure bigger than AH, lower surface area, lower water-molecule absorption, higher surface states and lower charge separation, all mixed AH + AR samples, which had physically-induced tuning in phase heterojunction, outperformed the commercial TiO2 P25 in acetaminophen (ATM) photodegradation efficiency. This could be due to effective charge separation and more active sites involved in AH + AR samples as seen in the depicted Z-scheme mechanism based on their band-edge positions obtained from Mott-Schottky analysis, scavenger tests and ATM photodegradation efficiency. In addition, this work also showed that band-edge positions, band-gap energy and heterojunction were correlated in determining the ATM photodegradation efficiency.

NFS-18. LOWER BODY SURFACE AREA IS ASSOCIATED WITH INCREASED LIKELIHOOD OF PLEXIFORM NEUROFIBROMA RESPONSE TO MEK INHIBITION

Abstract BACKGROUND MEK inhibitors (MEKi) are altering the management approach for plexiform neurofibroma (PN), with high rates of treatment response to multiple MEKi. Despite these successes, a subset of PN fail to respond and little is known about the clinical features associated with treatment response. METHODS We performed a retrospective cohort study integrating clinical trial data (NCT01362803, NCT02407405, NCT02096471, NCT03231306, NCT03363217) to identify baseline clinical features associated with response of PN to MEKi. Partial response (PR) was defined as ≥20 percent reduction in tumor volume from baseline. RESULTS Of 232 eligible participants, adequate clinical trial and imaging data was available for 223 participants. In the primary analysis of 184 participants with central response evaluation, the median age was 15.2 years with a median tumor volume of 488 milliliters at clinical trial enrollment. One hundred and eighteen (64%) participants achieved a PR with median time to PR of 8 cycles. Thirty-five participants (19%) required a dose reduction prior to 6 cycles of therapy due to toxicity. Younger age and lower body surface area (BSA) were significantly associated with PR in univariate analysis while female sex and typical PN appearance (versus nodular) on imaging approached significance. In multivariable analysis, only lower BSA was significantly associated with response while typical PN appearance approached significance. In the multivariable analysis of pediatric participants treated per BSA-based dosing, lower BSA was the only feature significantly associated with PR. In the expanded analysis of all 223 participants, lower BSA and typical PN appearance were significantly associated with PR. CONCLUSION Lower BSA and typical appearance of PN were associated with PR to MEK inhibitors. Future studies of MEK inhibitor for PN should integrate tumor pharmacokinetic-pharmacodynamic analyses to prospectively explore the impact of BSA on treatment response.

Adsorptive features of cyclohexane carboxylic naphthenic acid on a novel cross-linked polymer developed from spent coffee grounds.

Naphthenic acids (NA) are organic compounds commonly found in crude oil and produced water, known for their recalcitrance and toxicity. This study introduces a new adsorbent, a polymer derived from spent coffee grounds (SCGs), through a straightforward cross-linking method for removing cyclohexane carboxylic acid as representative NA. The adsorption kinetics followed a pseudo-second-order model for the data (0.007gmin-1mg-1), while the equilibrium data fitted the Sips model ( = 140.55mgg-1). The process's thermodynamics indicated that the target NA's adsorption was spontaneous and exothermic. The localized sterical and energetic aspects were investigated through statistical physical modeling, which corroborated that the adsorption occurred indeed in monolayer, as suggested by the Sips model, but revealed the contribution of two energies per site ( ). The number of molecules adsorbed per site ) was highly influenced by the temperature as decreased with increasing temperature and increased. These results were experimentally demonstrated within the pH range between 4 and 6, where both C6H11COO-(aq.) and C6H11COOH(aq.) species coexisted and were adsorbed by different energy sites. The polymer produced was naturally porous and amorphous, with a low surface area of 20 to 30 m2g-1 that presented more energetically accessible sites than other adsorbents with much higher surface areas. Thus, this study shows that the relation between surface area and high adsorption efficiency depends on the compatibility between the energetic states of the receptor sites, the speciation of the adsorbate molecules, and the temperature range studied.

Negligible adsorption and toxicity of microplastic fibers in disinfected secondary effluents

Wastewater treatment plants play a crucial role in controlling the transport of pollutants to the environment and often discharge persistent contaminants such as synthetic microplastic fibers (MFs) to the ecosystem. In this study, we examined the fate and toxicity of polyethylene terephthalate (PET) MFs fabricated from commercial cloth in post-disinfection secondary effluents by employing conditions that closely mimic disinfection processes applied in wastewater treatment plants. Challenging conventional assumptions, this study illustrated that oxidative treatment by chlorination and ozonation incurred no significant modification to the surface morphology of the MFs. Additionally, experimental results demonstrated that both pristine and oxidized MFs have minimal adsorption potential towards contaminants of emerging concern in both effluents and alkaline water. The limited adsorption was attributed to the inert nature of MFs and low surface area to volume ratio. Slight adsorption was observed for sotalol, sulfamethoxazole, and thiabendazole in alkaline water, where the governing adsorption interactions were suggested to be hydrogen bonding and electrostatic forces. Acute exposure experiments on human cells revealed no immediate toxicity; however, the chronic and long-term consequences of the exposure should be further investigated. Overall, despite the concern associated with MFs pollution, this work demonstrates the overall indifference of MFs in WWTP (i.e., minor effects of disinfection on MFs surface properties and limited adsorption potential toward a mix of trace organic pollutants), which does not change their acute toxicity toward living forms.

Hydrochar Production Methods: Comparative Insights into Hydrothermal and Microwave Processes

This study compares hydrochar production from agricultural waste using conventional hydrothermal carbonization (HTC) and microwave-assisted carbonization methods. Wheat straw (HWS), rice straw (HRS), and bagasse (HBG) were used as feedstocks. Microwave-assisted carbonization resulted in higher yields and distinct chemical structures compared to conventional HTC. Microwave hydrochars (m-HWS, m-HRS, mHBG) showed lower surface areas but increased pore volumes and thermal stability. They also exhibited enhanced heavy metal adsorption capacities, particularly at higher pH levels. These findings highlight the advantages of microwave-assisted carbonization for producing hydrochar with superior properties, offering insights for optimizing production processes and expanding applications.

Numerical investigation on the hydrogen removal capability of various catalytic elements in PARs

As an essential part of hydrogen removal system in nuclear power plants, PARs could effectively eliminate released hydrogen and prevent potential hydrogen combustion during severe accidents. Serving as a basic composition in the catalytic section of PARs, catalytic element has a direct influence on the hydrogen removal capability of the PAR device. The CFD software STAR-CCM+ was utilized to develop models of catalytic channels containing three common catalytic elements (including catalytic plates, catalytic cylinders, and catalytic spheres). The elementary reaction mechanism was employed as the reaction kinetics model to define the chemical reaction process. This paper aims to evaluate the hydrogen removal capability of the catalytic elements in same operating conditions and analyze important factors for designing the structure of catalytic elements. All the catalytic surface area of catalytic elements was set to 0.045 m2 and inlet boundary conditions were settled identically. Our findings show that catalytic sphere exhibits the best hydrogen removal capability, which is attributed to the large lower half catalytic surface area of spheres. Catalytic plate with a lower height also demonstrates excellent hydrogen removal capability because of the presence of a larger catalytic area in the leading section. However, the hydrogen removal capability of catalytic cylinder is affected by the boundary layer separation vortex. A noticeable decrease in reaction rate occurs on the lower part of the sidewall surface, especially in the catalytic cylinder with a larger radius. In the structure design of catalytic elements, enlarging the catalytic surface area in the leading section and avoiding boundary layer separation on the catalytic surface are essential to further improve the hydrogen removal capability.

Metal organic framework-derived porous Ni-doped In2O3 for highly sensitive and selective detection to hydrogen at low temperature

Achieving high sensitivity and selective detection at low temperature is of great significance for hydrogen leakage monitoring and early warning. As a very promising hydrogen sensitive material, In2O3 still faces great challenges in achieving high-performance hydrogen sensing at low temperatures due to inherent defects such as low specific surface area and limited active sites. Here, we prepared Ni-doped In2O3 mesoporous nanomaterials using metal organic framework (MOF) as sacrificial templates. The prepared Ni-doped In2O3 exhibited mesoporous structures with small diameters (2–3 nm), which could be used as effective molecular sieves for the selective detection of hydrogen. The high specific surface area (72.0 m²/g) provided numerous active sites for surface redox reactions, resulting in a remarkable hydrogen sensing response. Notably, gas sensitivity tests demonstrated that the Ni-doped In2O3 gas sensor achieved optimal hydrogen detection performance at 100°C. Particularly, the 3 at% Ni-doped In2O3 nanomaterials exhibited a high response of 12.5–100 ppm hydrogen, along with favorable response/recovery time and a practical limit of detection down to 5 ppm. Furthermore, the Ni-doped In2O3 sensor exhibited excellent reversibility, reproducibility, selectivity and long-term stability. In addition, simulation calculations based on molecular dynamics (MD) and density functional theory (DFT) show that molecular sieve effect is the main reason for the enhanced selectivity, and Ni doping induced oxygen vacancy (OV) defects could enhance gas adsorption. This work could provide technical support for leak detection and warning during hydrogen use, storage and transportation in the future.

Graphene Oxide as Novel Visible Light Active Photocatalyst: Synthesis, Modification by Nitrogen and Boron Doping, and Photocatalytic Application

Graphene oxide (GO) has become one of the emerging and important sole photocatalyst nanomaterials in recent years due to its exceptional/tunable optoelectronic properties, multifunctionality, and eco‐friendly nature. However, challenges remain in tuning surface chemistry, tailoring the band gap, developing doping strategies, and understanding the sole photocatalytic mechanism. This contribution investigated the synthesis of GO via the improved Hummers method by varying the ratio of the oxidizing agents (K2Cr2O7:KMnO4), as well as modifications by nitrogen (N) and boron (B) doping in view of its applications in photocatalytic degradation of organic dye pollutants. Furthermore, changes in surface chemistry, optical, compositional, morphological, and structural properties are investigated to understand the photocatalytic mechanism. The synthesized GO showed a broad spectrum of light absorption with a tunable band gap of 2.4–4.3 eV and exhibited more than 91% degradation of methylene blue dye under direct sunlight. However, the photocatalytic activity decreased after N and B doping attributed to reduced oxygen‐containing functional groups, low surface area, and dopants‐induced bonding configurations within the GO structure. This study provides a new insight into replacing metallic semiconductor photocatalysts with highly affordable, environmentally friendly, and potent metal‐free GO photocatalysts.

Excellent adsorption and catalytic oxidation of toluene facilitated by metal-free nitrogen-doped mesoporous biochar

In this study, we synthesized a series of nitrogen-doped mesoporous biochar by a salt-templating method to assess the potential of our modified biochar for advanced remediation of toluene through either adsorption or catalytic oxidation. The principal findings indicated that the incorporation of nitrogen and the mesopore-forming agent significantly influenced the toluene removal performance by altering the physicochemical properties of the biochar. Notably, the sample synthesized at 900 °C (BUPZ-900) exhibited the exceptional toluene adsorption capacity, reaching 283.85 mg/g, due to its high surface area and mesopore volume. Advanced characterizations revealed that different nitrogen functionalities played distinct roles in the adsorption performance. The presence of graphitic nitrogen in BUPZ-900 enhanced toluene adsorption through π-π dispersion interactions. Conversely, BUPZ-600, boasting a high nitrogen content (8.66 at%) and a predominance of pyridinic-N (3.92 at%), exhibited the highest catalytic activity, despite its low adsorption capacity attributed to a smaller surface area. This heightened activity was attributed to the basicity of pyridinic-N, which acted as active sites, despite the material’s lower surface area. Our study highlights the promise of nitrogen-doped mesoporous biochar as an effective adsorbent or catalyst for advanced remediation of volatile organic compounds (VOCs), even in the absence of metal catalysts. This work emphasizes the critical role of synthesis temperature and nitrogen functionalization in optimizing biochar properties for environmental applications.

Identification of influential parameters and conditions in heavy metals adsorption onto Cal-LDH-PC using optimization approaches of RSM and Taguchi

Adsorption process plays an important role in the remediation of heavy metals (HMs) from wastewater. A laboratory trial was conducted to investigate effective parameters for improving the bio-adsorption removal of HMs. SEM, EDX, BET, and FTIR techniques were applied to characterize the calcined layer double hydroxide (Cal-LDH), pectin (PC), and Cal-LDH-PC composite prepared from Licorice pomace. The adsorption of zinc (Zn) cadmium, nickel (Ni) and lead (Pb) onto the most efficient sorbent was investigated using RSM methodology with operational factors such as concentration, reaction time, sorbent dose, and pH. The results related to FTIR showed that Cal-LDH-PC had the highest number of functional groups. Based on the SEM results Cal-LDH had a low surface area (9.36 m2 g-1) and a small pore size (9.22 nm). After the modification process (Cal-LDH-PC), the values of surface area and pore size increased by 13-fold (120 m2 g-1) and 1.5-fold (18 nm), respectively. Cal-LDH had high adsorption performance, more cavities, stability, various functional groups, and excessive carbon and oxygen content, which make it efficient and powerful in removing HMs from wastewater. The optimal condition for achieving the removal efficiency (RE%) values of metals was determined to be 80.79 mg L−1, 100 min, 0.167 g L−1, and 9 for concentration, reaction time, sorbent dose, and pH, respectively. Maximum adsorption capacity and RE (%) were 300 mg g−1 and 99% for Zn. According to the results concentration had a major impact on RE% (except for Ni), while for Ni, adsorbent dose had the most significant impact. The present study introduced Cal-LDH-PC prepared from Licorice pomace as a capable, useful and economical sorbent for HMs removal from polluted environments. Taguchi's statistical method is distinguished as an economic method with easier interpretation, while the RSM approach is more accurate, and it can also check the interaction of parameters.

Hydrophobic Modification of Pectin Aerogels via Chemical Vapor Deposition.

Pectin aerogels, with very low density (around 0.1 g cm-3) and high specific surface area (up to 600 m2 g-1), are excellent thermal insulation materials since their thermal conductivity is below that of air at ambient conditions (0.025 W m-1 K-1). However, due to their intrinsic hydrophilicity, pectin aerogels collapse when in contact with water vapor, losing superinsulating properties. In this work, first, pectin aerogels were made, and the influence of the different process parameters on the materials' structure and properties were studied. All neat pectin aerogels had a low density (0.04-0.11 g cm-1), high specific surface area (308-567 m2 g-1), and very low thermal conductivity (0.015-0.023 W m-1 K-1). Then, pectin aerogels were hydrophobized via the chemical vapor deposition of methyltrimethoxysilane using different reaction durations (2 to 24 h). The influence of hydrophobization on material properties, especially on thermal conductivity, was recorded by conditioning in a climate chamber (25 °C, 80% relative humidity). Hydrophobization resulted in the increase in thermal conductivity compared to that of neat pectin aerogels. MTMS deposition for 16 h was efficient for hydrophobizing pectin aerogels in moist environment (contact angle 115°) and stabilizing material properties with no fluctuation in thermal conductivity (0.030 W m-1 K-1) and density for the testing period of 8 months.