Impregnation Technique Research Articles

Evaluation of a novel nickel ceramic filter prepared by urea precipitation method for removal of tars from biomass syngas using naphthalene as tar model compound

Gasification has been shown to be an effective thermal conversion process for waste biomass in order to create fuel, specialty chemicals, and hydrogen. Gasification is likely to take on a major role in the near future in the burgeoning hydrogen economy. In order to improve the commercial viability of gasification, catalytic tar reforming has come to the forefront as one of the most promising methods of reducing the tar content that has been detrimental to downstream equipment in the process. The use of catalytic ceramic filters has presented promising potential for this application that can serve dual role of tar and particulate removal. In this study, a nickel-based ceramic filter has been prepared using urea vacuum impregnation technique and evaluated for tar removal efficiencies. The urea technique was more effective than traditional impregnation techniques at uniformly dispersing nickel across the surface of the ceramic filter, driving the nickel particles to penetrate the pores of the support, thus aiding in improved tar removal capabilities. Through steam reforming studies using a naphthalene simulant tar molecule, the 15 wt% nickel filter was able to reduce the naphthalene content by 97% at temperature of 750 °C over 2 h. An activation energy of 126.4 kJmol was achieved for steam reforming using the urea vacuum impregnated catalytic filter compared to 136.4 kJmol using the incipient wetness impregnated filter.

A sulfur-modified pore-blocking method to enhance the electrocatalytic stability of carbon-supported platinum nanoparticles.

Currently, the durability of electrode materials remains a big obstacle to the widespread adoption of proton exchange membrane fuel cells (PEMFCs). Herein thiourea and sodium dodecyl benzene sulfonate (SDS) were employed as sulfur source and carbon source to modify the pristine carbon black (Ketjen black EC300 J). A highly durable carbon supported Pt nanosized catalyst with higher platinum utilization for oxygen reduction reaction (ORR) in PEMFCs was produced by doping elemental sulfur into carbon supports and decreasing the carbon pore sizes and volume through a successive impregnation technique. The catalyst exhibits an initial activity of 0.167 A mgPt -1 at 0.90 V and demonstrates minimal activity loss after acceleration stress test (30,000 cycles of AST). The half-wave potential loss for representative sample (Pt/S-C-3) is only 14 mV with only 21.8 % ECSA decrease, 27.5 % MA loss and 5.9 % SA loss. A sintering test at various temperature shows a minor average size increase for sulfur-doped carbon (S-C) supported one (from 2.09 to 2.52 nm). In single-cell test, the MEA sample employing the platinum catalyst on modified carbon as cathode exhibited almost negligible performance loss after 30,000 cycles of AST.

Influence of Slurry Impregnation Technique of Recycled Concrete Aggregates on the Roller Compacted Concrete Pavement

Influence of Slurry Impregnation Technique of Recycled Concrete Aggregates on the Roller Compacted Concrete Pavement

Enhancing Water Resistance in Foam Cement through MTES-Based Aerogel Impregnation.

The propensity of foamed concrete to absorb water results in a consequential degradation of its performance attributes. Addressing this issue, the integration of aerogels presents a viable solution; however, their direct incorporation has been observed to compromise mechanical properties, attributable to the effects of the interface transition zone. This study explores the incorporation of MTES-based aerogels into foamed cement via an impregnation technique, examining variations in water-cement ratios. A comprehensive analysis was conducted, evaluating the influences of MTES-based aerogels on the thermal conductivity, compressive strength, density, chemical composition, and microstructure of the resultant composites across different water-cement ratios. Our findings elucidate that an increment in the water-cement ratio engenders a gradual regularization of the pore structure in foamed concrete, culminating in augmented porosity and diminished density. Notably, aerogel-enhanced foamed concrete (AEFC) exhibited a significant reduction in water absorption, quantified at 86% lower than its conventional foamed concrete (FC) counterpart. Furthermore, the softening coefficient of AEFC was observed to surpass 0.75, with peak values reaching approximately 0.9. These results substantiate that the impregnation of MTES-based aerogels into cementitious materials not only circumvents the decline in strength but also bolsters their hydrophobicity and water resistance, indirectly enhancing the serviceability and longevity of foamed concrete. In light of these findings, the impregnation method manifests promising potential for broadening the applications of aerogels in cement-based materials.

Development of the Sb4O5Cl2@NbSe2 Composite: The Impact of 2H-NbSe2 Nanoparticles on Sb4O5Cl2 and Their Application for the Removal of Cr(VI)/Fe(III) and Methyl Orange from Wastewater.

A potential adsorbent, Sb4O5Cl2@NbSe2 composite, was generated from the Sb4O5Cl2 photocatalyst and 5 wt % layered 2H-NbSe2 nanoparticles for the highly effective removal of Cr(VI) and Fe(III) ions and methyl orange (MO) from aqueous solution, and a comparison was drawn against the precursors. Sb4O5Cl2 crystallites and NbSe2 nanoparticles were synthesized hydrothermally, and the composite was prepared by the incipient wetness impregnation technique. The crystal structure of Sb4O5Cl2 was determined by single-crystal X-ray diffraction (SCXRD) data. Powder X-ray diffraction (PXRD) study revealed the 2H phase of NbSe2 nanoparticles. Field emission scanning electron microscopy (FESEM) analysis confirmed the formation of the spherical-shaped NbSe2 nanoparticles from rod-shaped bulk 2H-NbSe2. Morphological changes from the hexagonal to irregular prismatic shape were found upon the formation of the Sb4O5Cl2@NbSe2 composite compared to pure Sb4O5Cl2. Negative ζ-potential values indicated that electrostatic interactions were the predominant factor for the adsorption process. Sb4O5Cl2@NbSe2 provided removal efficiencies of 99% for MO in 6 h, 96.52% for Cr(VI) within 2.5 h, and 92.43% for Fe(III) within 4 h of 10 mg/L initial concentration. The maximum adsorption capacities of the composite for MO, Fe(III), and Cr(VI) were found to be 66.56, 131.48, and 122.30 mg/g, respectively, as calculated using the Langmuir isotherm equation.

Valorization of durian peel as a carbon feedstock for a sustainable production of heterogeneous base catalyst, single cell oil and yeast-based biodiesel

The present study reports a successful attempt to produce single cell oil (SCO), heterogeneous base catalyst and yeast-based biodiesel from durian peel as a promising carbon feedstock by means of the waste-to-energy concept. For this purpose, first, durian peel (DP) was hydrolyzed by dilute sulfuric acid to obtain xylose-rich DP hydrolysate (XDPH) and post-hydrolysis DP solid residue (DPS). Candida viswanathii PSY8, a newly isolated oleaginous yeast, showed high SCO accumulation (5.1 ± 0.1 g/L) and SCO content (35.3 ± 0.13 %) on undetoxified XDPH medium. A novel heterogeneous base catalyst (DPS-K) prepared from DPS by wet impregnation technique with KOH, exhibited considerable catalytic activity to convert SCO-rich wet yeast of C. viswanathii PSY8 into yeast-based biodiesel (FAME) via direct transesterification with a maximum FAME yield of 94.3 % under optimal conditions (6 wt% catalyst, 10:1 methanol to wet yeast ratio, 75 °C, and 2 h). Moreover, most of the yeast-based biodiesel properties obtained from the FAME profiles were correlated well with the biodiesel standards limit of Thai, ASTMD6751 and EN 14214. Additionally, the energy output of FAME produced about 37.5 MJ/kg was estimated. Thus, this present finding demonstrated the favorable strategy for sustainable and eco-friendly production of new generation biodiesel.

Novel Cerium (IV) Oxide -Ti3C2- titanium dioxide heterostructure photocatalyst for pharmaceutical pollutants removal: Photocatalyst characterization, process optimization and transformation pathways

Tetracycline (TC) is a widely applied antibiotic recognized for its potential negative consequences on human health and ecological balance. In this study, a novel photocatalyst, Cerium (IV) oxide -Ti3C2- titanium dioxide (CeMXT), was synthesized through sonochemical and impregnation techniques, subsequently subjected to comprehensive characterization employing diverse methods including XRD, SEM, TEM, HR-TEM, Raman, XPS, and BET. The optimization of TC degradation was pursued using the Response Surface Methodology (RSM), encompassing variables such as initial TC concentration, irradiation duration, photocatalyst dosage, and pH. The degradation efficacy was investigated through free radical trapping experiments, revealing the pivotal roles of OH and superoxide anion radicals. Remarkable degradation efficiency, reaching 94.70 %, was achieved under specific parameter conditions: 22.19 mg/L TC concentration, 104.13 min irradiation, 0.65 g/L photocatalyst dosage, and pH 4.72. This exceptional performance could be attributed to the elevated generation of oxidant species facilitated by the Z-scheme electron transfer heterojunction. Furthermore, LC-Mass analysis was employed to delineate the intermediates formed during TC photodegradation, culminating in proposing a conceivable degradation pathway. The impressive proficiency of the CeMXT photocatalyst underscores its potential application for effective large-scale treatment of persistent organic pollutants in wastewater treatment facilities. Additionally, comparative analysis with a recently developed photocatalyst highlights its promise as a viable alternative for the remediation of such contaminants in aquatic ecosystems.

Metal–organic framework‐supported hydroxyapatite (UiO‐66@HAp): an efficient catalyst for the microwave‐assisted transesterification of palm oil

AbstractBiodiesel has recently emerged as a renewable and environmentally benign fuel substitute for fossil‐derived energy sources. The use of heterogeneous solid catalysts for the generation of biodiesel from biomass‐derived fats and oils is sustainable. Among various reported catalyst supports, metal–organic frameworks (MOFs) have been popular choices for enhancing catalytic activity for biodiesel synthesis because of several outstanding features including porosity, high surface area, adjustable structures, and uniform pore sizes. In this research, the authors synthesized a novel nanocomposite of MOF‐supported hydroxyapatite (UiO‐66@HAp) using a facile impregnation technique and the characterization of the as‐synthesized catalyst was performed by different spectroscopic methods including powder X‐ray diffraction (PXRD), Fourier transform infrared (FTIR), X‐ray photoelectron spectroscopy (XPS), field emission gun‐scanning electron microscope (FEG‐SEM), energy dispersive X‐ray spectroscopy (EDS), high resolution transmission electron microscopy (HR‐TEM), thermogravimetric analysis (TGA), and N2 adsorption–desorption techniques. After successful synthesis, the catalytic property of the prepared material was evaluated in the palm oil transesterification into biodiesel. Product formation was confirmed by the 1H nuclear magnetic resonance (NMR) spectroscopy, 13C NMR, FTIR, and gas chromatography–mass spectrometry (GC–MS) of the biodiesel. The influence of different reaction variables such as catalyst dosage, methanol/oil molar ratio, temperature of the reaction, and reaction time was also studied. The outcomes revealed that the maximum biodiesel yield (∼97%) was obtained when 6 wt% catalyst was used with a 6:1 ratio of methanol/oil at 70 °C for 1 h. It was also observed that, even after 5 cycles of reuse, the catalyst was capable of producing significant amounts of biodiesel (over 90%). The results suggest that the synthesized novel catalyst holds a promising future in the sustainable production of biodiesel.

Cr2O3- TiO2 nanocomposite made using plant (Oats) extract via impregnation technique for photocatalytic activity of hydrogen production

In this study an efficient photocatalyst of water splitting was developed. It's discussed. The Cr2O3 with TiO2nanoparticles (Cr2O3-TNPs) nanocomposite with (Oats extract) were created using ecologically friendly methods impregnation technique such TiO2 exhibits nanospherical (TNPs) shape structure. This nanocomposite material enhanced their ability to absorb ultraviolet light while also speeding up the recombination of photogenerated electrons and holes, according to the researchers. The TNPs and prepared Cr2O3-TNPs were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy dispersive x-ray spectroscopy (EDX), and UV-visible absorbance. The XRD of TNPs showed a Tetragonal phase with 8.9 nm of average crystallite size,. FE-SEM images showed that the average particles size in the range of 22.5 nm and UV-VIS absorbance have energy gaps are 3.9eV while the energy gaps of Cr2O3-TNPs smaller than that 3.6 eV. It was found that the performance of photocatalysts of the nanocomposite for hydrogen generation was superior, as it gave the highest rate of hydrogen production (6.3) ml at 80 min when exposed to ultraviolet light. Moreover, the nanocomposite revealed the high H2 production rate under ultraviolt light irradiation (λ < 400 nm), The Cr2O3-TNps have a high photocatalytic effectiveness due to their wide ultraviolt light photoresponse range and excellent separation of photogenerated electrons and holes.

Novel Nanostructured Pd/Co-Alumina Materials for the Catalytic Oxidation of Atmospheric Pollutants.

Cobalt-doped alumina catalysts were prepared using different methods, either conventional wet impregnation (WI) and/or advanced spray impregnation (SI), and they were evaluated as novel oxidation catalysts for CO and MeOH oxidation. The spray impregnation technique was used with the aim of achieving the synthesis of core-shell catalytic nanostructures to secure the chemical/thermal stability of active sites on the catalyst carrier. The catalysts were further promoted with a low Pd content (0.5 wt.%) incorporated via either incipient wetness impregnation (DI) or spray impregnation. The results revealed the superior performance of the spray-impregnated catalysts (Co/γ-Al2O3-SI) for both reactions. The deposition of Co oxide on the outer surface of the alumina particle (SEM images) and the availability of the active Co phase resulted in the enhancement of the Co/γ-Al2O3 catalysts' oxidation activity. Pd incorporation increased the catalysts' reducibility (TPR-H2) and improved the catalysts' performance for both reactions. However, the Pd incorporation method affected the catalytic performance; with the SI method, the active phase of Co3O4 was probably covered with PdO and was not available for the oxidation reactions. On the contrary, the incorporation of Pd with the DI method resulted in a better dispersion of PdO all over the Co/Al catalyst surface, maintaining available Co active sites and a better Pd-Co interaction. MeOH desorption studies revealed the methanol oxidation mechanism: the Co/Al catalysts promoted the partial oxidation of MeOH to formaldehyde (HCHO) and dehydration to dimethyl ether (DME), while the Pd-based Co/Al catalysts enhanced the complete oxidation of methanol to CO2 and H2O.

Potato cubes for the elderly with dysphagia designed through freeze-thaw impregnation technique: Effect of enzymatic hydrolysis

This study aimed to evaluate the effects of enzymatic hydrolysis on the chewing and swallowing properties of potato cubes using a freeze-thaw impregnation technique. The texture properties, microstructure, rheological properties, and suitability as a dysphagia diet of the potato cubes after enzymatic hydrolysis were studied. The results indicated that pectinase reduced the texture of the potato cubes more than cellulase and α-amylase. Pectinase hydrolysis could improve the safety of potato cubes as food for the elderly. Pectinase improved the stability of the mashed potatoes by increasing their viscosity and elastic modulus after chewing, thus improving their swallowing properties. The concentration at 200 U/mL and the hydrolysis time at 60 min were the best hydrolysis condition for pectinase to make dysphagia-suitable potato cubes. This study provides insights into the development of potato-based foods that can be used as dysphagia diet for the elderly.

Research on structural strengthening technology for regenerative denitration catalysts.

The cost of replacing failed selective catalytic reduction (SCR) catalysts and their disposal as hazardous solid waste is high. If failed catalysts are recovered and regenerated into new SCR denitration catalysts, the cost of flue gas denitration can be effectively reduced. However, regenerated SCR catalysts have relatively low structural strength and activity and cannot yet form an effective replacement. In this study, aluminum dihydrogen phosphate, aluminum nitrate, and aluminum sulfate were used as structural strengthening agents in the regeneration of SCR catalysts, and over-impregnation, drumming-assisted impregnation, and ultrasonic-assisted preparation techniques were compared. The corresponding regenerated SCR catalysts were then prepared and analyzed for compressive strength, wear strength, H2-TPR, NH3-TPD, and in situ IR. Factors influencing the structural strength, physical properties, and catalytic activity of the regenerated catalysts were investigated. The best results were obtained as follows: compressive strength of 4.57 MPa, wear rate of 0.088% kg-1, and denitration of 58% after 10 min of drumming-assisted impregnation in an aluminum sulfate solution with a concentration of 16%. Based on this, a synergistic method for catalyst activity and structural strengthening was explored to support the design of better SCR catalysts for regeneration.

Potential of vacuum impregnation and osmotic dehydration techniques in producing jaggery-fortified apple snacks

Jaggery is proposed as a non-conventional osmotic agent to produce nutritious sustainable apple snacks via vacuum impregnation and osmotic dehydration, followed by air drying or freeze drying.

Construction of MXene-enhanced rigid polyurethane foam/polyethylene glycol phase change composites for solar thermal conversion and storage

In this study, various rigid polyurethanes foams (PUFs) with different morphologies were prepared and subsequently used for encapsulating the phase change material, polyethylene glycol (PEG). To address the low photothermal conversion efficiency of polyurethane-based phase change materials, MXene was successfully synthesized via an in-situ hydrofluoric acid (HF) etching method and incorporated into the PEG to obtain MXene@PEG composite material. Finally, a series of innovative MXene@PEG-PUF phase change composites were successfully fabricated by utilizing PUFs as the supporting matrix and the MXene@PEG composite as the phase change component through a vacuum impregnation technique, and their thermophysical properties and photothermal conversion performance were systematically studied. The results show that PUF is the ideal capsulation material for PEG. And MXene@PEG-PUF demonstrates a high PCM loading rate (>80 wt%) and a high latent heat storage enthalpy (>140 J/g) with a relative enthalpy efficiency of 99.5%, maintaining excellent shape stability and relative enthalpy efficiency of 95.58% after 150 thermal cycles. This highlights its superior thermal reliability, making it suitable for practical building energy-saving applications. Most importantly, the incorporation of MXene into PUF@PEG significantly enhances solar-to-thermal conversion capability, attributed to the exceptional photothermal characteristics of MXene.

Transforming Wood into a High-Performance Engineering Material via Cellulose Nanocrystal Impregnation

Abstract The demand for wood in construction has led to shortages of strong wood types, causing a shift to costlier alternatives like concrete and nonbiodegradable materials, prompting the investigation of modifying softwoods for better engineering properties. This study investigates the optimization of a multistep impregnation process utilizing functionalized cellulose nanocrystals (f-CNCs) to enhance softwood properties. The process involves alkali delignification, ultrasonication, and vacuum pressure treatment to improve wood porosity and in turn improve CNC impregnation with uniform dispersion. Microstructural analyses through field emission scanning electron microscopy and atomic force microscopy (AFM) offer detailed insights into cell wall morphology and surface topography, whereas Fourier transform infrared spectroscopy highlights compositional shifts resulting from f-CNC impregnation. Mechanical testing demonstrates significant improvements for treated woods, particularly a 67 percent increase in modulus of elasticity for the 2 percent CNC-treated group compared with the control group; a 71 percent increase in modulus of rupture was observed for 2 percent CNC-, 3 percent NaOH-, and 2 percent acetic acid-treated group compared with the control sample. The sample delignified with 3 percent NaOH and impregnated by 2 percent f-CNC emerged as particularly effective. This research sets the stage for potential advancements in strengthening softwood using CNC, including a novel AFM method and alternative impregnation techniques like the Lowry method, inviting further exploration.

Significantly advanced hydrogen production via water splitting over Zn/TiO2/CNFs and Cu/TiO2/CNFs nanocomposites

Photocatalytic water splitting using solar radiation has drawn considerable attention for production of hydrogenbecause of minimal carbon emissions, however huge limitations that still exist are low light harnessing catalysts and high recombination rate of the photo-generated charge carriers. This study focuses on the fabrication of nanomaterials for advanced photocatalytic water splittingas a result, structures of TiO2/CNFs, Cu/TiO2/CNFs, and Zn/TiO2/CNFs nanocomposites of mesoporous nature were synthesized using CNFs and surfactant wrapping sol–gel/hydrothermal method. Impregnation technique was used in copper and zinc loading while characterization of the synthesized catalysts was achieved by XRD, Raman, FESEM, TEM, UV/DRS, BET, FTIR, XPS, and PL techniques. Water splitting was performed byUV light irradiation and the effect of compositing TiO2/CNFs-Cu/Znevaluated. 10 %_TiO2/CNFs/5%Zn composite was the most efficient photocatalyst for hydrogen production when compared with the rest of the samples. 10 %_TiO2/CNFs/5%Zn, 0.53 mol (h g cat.)-1, was 90–100 folds the amount generated over commercial TiO2 – P25, and pure TiO2photocatalysts. The improved photo-activity of the TiO2/CNFs, Cu/TiO2/CNFs, and Zn/ TiO2/CNFs composites were due to the synergistic effect between Cu, Zn and CNFs.This work gives promising route for fabricating TiO2/CNFs/metal (Cu, Zn) composites for advanced H2production using UV-radiation.

Oxidative Desulfurization of Simulated Diesel Fuel by Synthesized Tin Oxide Nano-Catalysts Support on Reduced Graphene Oxide

The modified Hummers method was applied to prepare graphene oxide (GO) from the graphite powder. Tin oxide nanoparticles with different loading (10-20 wt.%) supported on reduced graphene oxide were synthesized to evaluate the oxidative desulfurization efficiency. The catalyst was synthesized by the incipient wetness impregnation (IWI) technique. Different analysis methods like FT-IR, XRD, FESEM, AFM, and Brunauer-Emmett-Teller (BET) were utilized to characterize graphene oxide and catalysts. The XRD analysis showed that the average crystal size of graphene oxide was 6.05 nm. In addition, the FESEM results showed high metal oxide dispersions on the rGO. The EDX analysis shows the weight ratio of Sn is close to its theoretical weight. The reduction of metal oxide and (GO) has occurred in one step at temperatures of 400 °C for 2 hours. The performance of the catalysts for dibenzothiophene (DBT) removal using H2O2 as an oxidizing agent was determined under a range of different operating conditions. The results showed that the maximum desulfurization was 71.68% in the best conditions (DBT concentration = 385 ppm, time = 90 min, temperature = 60 oC, catalyst dosage = 0.04g, and amount of oxidant = 0.375 ml).

Coal fly ash-supported ZnO-promoted TiO2 towards UV photocatalytic degradation of anthraquinone dye: Parametric optimization, kinetics and mechanism studies

Heterogeneous photocatalysis via combination of catalyst and UV irradiation is one of the most promising advanced oxidation processes for degradation of water-soluble organic contaminants. Herein, different photocatalysts (ZnO/CFA, TiO2/CFA, and TiO2-ZnO/CFA) were synthesized via sol-gel and impregnation techniques and applied for the degradation of acid blue 25 (AB25) dye in aqueous solution under UV light in a photoreactor. Various spectroscopic techniques (XRF, XRD, BET, FTIR, UV–vis DRS, TEM and EDS) were employed to evaluate the chemical structure, functional groups, textural, and optical properties of the binary and ternary composites. TiO2-ZnO/CFA displayed rapid degradation of AB25 as compared to ZnO/CFA and TiO2/CFA, owing to the dualistic photocatalytic sites. The prepared TiO2-ZnO/CFA composite was used in synergy with the photoreactor for photocatalytic degradation process optimization, and the optimum degradation conditions in relation to initial AB25 concentration (10 mg/L), UV light intensity (18 W/m2), flow rate (12.5 L/h), and irradiation time (150 min) as input parameters were determined using Taguchi design approach. The maximum photocatalytic degradation efficiency was 98.79±0.94% under those aforementioned conditions, indicating that the synergies between the photoreactor and the TiO2-ZnO/CFA photocatalyst resulted in the effective destruction of AB25 dye molecules. Furthermore, the spent photocatalyst was easily removed from the degraded solution and reused up to nine times. After 150 mins of UV irradiation with TiO2-ZnO/CFA photocatalyst, almost complete mineralization of AB25 solution was achieved.

CoFe2O4 nanoparticles modified amidation of N-doped carbon nanofibers hybrid catalysts to accelerate electrochemical kinetics of Li-S batteries with high sulfur loading

Lithium-sulfur battery have been considered as promising energy storage devices because of its superiority in energy density. However, the low active material utilization, low sulfur loading, shuttle effect and torpid kinetics of polysulfides, and poor cycling stability limit its commercial applications. Herein, the functionalized nitrogen doped carbon nanofibers containing amide groups were designed by electrospun and polyamidoamine dendrimer (PAMAM) solution impregnation techniques. The obtained amide groups modified nitrogen-doped carbon nanofibers (ANF) were combined with spinel CoFe2O4 (CFO) nanoparticles (CFOANF) via hydrothermal method to design as membrane electrode containing Li2S6 catholyte for lithium-sulfur batteries. The introduction of nitrogen doped and amide groups modified ANF can increase fibers polarity, which have chemical adsorption capability toward lithium polysulfides. CFO nanoparticles can further absorb the soluble polysulfides by strong chemical interaction due to its intrinsic polarity and also serve as a catalyst to promote the redox kinetics of polysulfides conversion. Benefiting from the synergism of the physical confinement, polar chemical adsorption, and catalytic conversion, the as-prepared CFOANF delivers excellent electrochemical performances at high sulfur loading. The as-prepared CFOANF membrane with 6.3 mg cm−2 sulfur loading delivers a high initial capacity of 940 mAh g−1 and excellent long-term cycling stability up to 450 cycles with a low decay rate 0.059 % per cycle at 0.2C. Remarkably, even at 12.6 mg cm−2 and 16.4 mg cm−2 sulfur loading, the CFOANF membrane electrodes show high capacity of 9.7 mAh cm−2 and 11.8 mAh cm−2, respectively. The results show that the chemically anchoring polysulfides and catalyzing redox reaction by multifunctional CFOANF hybrid composite is promising for assembling with a high sulfur loading electrode, which exhibits a superior electrochemical performance in lithium-sulfur batteries.

Effect of Ni/Al-MCM-41 Impregnation Method on Catalytic Deoxygenation of Reutealis Trisperma Oil

Deoxygenation of Reutealis trisperma oil into green diesel has been carried out using Ni/Al-MCM-41 catalyst. The Ni/Al-MCM-41 catalyst was prepared using the wetness impregnation and incipient wetness impregnation methods, hereinafter referred to as Ni/Al-MCM-41 (WI) and Ni/Al-MCM-41 (IWI). XRD and FTIR analysis shows a characteristic of amorphous phase for solid Al-MCM-41 catalyst. FTIR pyridine was used to assess the impact of the NiO impregnation technique on Lewis acid and Brønsted acidity. The acidity test showed that the Ni/Al-MCM-41 (WI) catalyst had the highest total acidity 0,227 mmol/g. The catalytic activity of Ni/Al-MCM-41 catalyst was examined in deoxygenation reaction of Reutealis trisperma oil under inert conditions for 4 hours. In comparison to Ni/Al-MCM-41(IWI) and Al-MCM-41 catalysts, the Ni/Al-MCM-41(WI) catalyst produced better results in the deoxygenation reaction of Reutealis trisperma oil with a selectivity of hydrocarbon compounds (C11-18) of 100% and a degree of deoxygenation of 92.77%.