Synergetic Effect Research Articles

Synergistic promotion of reaction kinetics for LiPSs at high loadings by interfacial built-in electric field and sulfur vacancies of ternary heterostructure for high-performance Li-S batteries

The practical application of lithium-sulfur batteries is significantly impeded by the chaotic migration of lithium polysulfides, sluggish redox-reaction kinetics, and pronounced shuttle effect. Herein, a ternary heterostructure (MoS2-x/MoO2/CoP) is developed with a spontaneous built-in electric field (BIEF) and enriched sulfur vacancies. This heterostructure comprises MoS2-x, which has a high adsorption capability and work function; CoP, noted for its low work function and potent catalytic properties; and MoO2, which features a work function between that of MoS2-x and CoP and serves as a bridge with excellent electronic conductivity. An appropriate combination of the catalyst and adsorbent with sulfur vacancies controls the direction of the BIEF, realizing the “adsorption-directed migration-catalytic” reaction mechanism for sulfur species. Specifically, the synergetic effect of the BIEF and sulfur vacancies enhances electron migration from CoP to MoS2-x, which improves the lithium polysulfide (LiPSs) trapping and accelerates the directional migration of LiPSs to CoP, thereby enabling the efficient catalytic conversion of sulfur species. Consequently, batteries equipped with MoS2-x/MoO2/CoP interlayers that contain sulfur vacancies demonstrate an ultrahigh initial specific capacity of 1356.2 mA h g−1 at 0.2 C, maintaining a capacity of 708.3 mAh g−1 after 1000 cycles at 2 C. Even with sulfur loading increased to 7.13 mg cm−2, these batteries display an initial specific capacity of 7.2 mAh cm−2. This work provides a feasible approach for the rational design of vacancy-containing ternary heterostructure catalysts for commercial lithium-sulfur batteries.

Thermodynamic and economic analysis of a novel solid oxide fuel cell, two level thermoelectric generator and double effect parallel absorption chiller integrated system

This study presents a comprehensive thermodynamic and economic analysis of a novel hybrid energy system integrating a Solid Oxide Fuel Cell (SOFC) with a Two-Level Thermoelectric Generator (TTEG) and a Double-Effect Parallel Absorption Chiller (DEPAC) for enhanced waste heat recovery. The primary objective is to maximize energy utilization and overall efficiency by leveraging the synergetic effects of these components. Unlike previous studies, this research uniquely evaluates the effectiveness of the integrated system and examines the impact of different Absorption Chiller configurations and the number of TTEG elements, filling a critical gap in the literature. The proposed system achieves a net electrical efficiency of 42.88 %, an energy efficiency of 44.61 %, and an exergy efficiency of 57.16 % under optimal conditions. This marks a significant improvement compared to standalone SOFC systems, with the TTEG effectively harnessing waste heat and contributing an additional 0.680 kW/m2 to the overall power output. The integration of the DEPAC system further enhances performance by providing cooling with a Coefficient of Performance (COP) of 1.351. The economic analysis reveals a positive Net Present Value (NPV) of $1,993,136, a Dynamic Payback Period (DPP) of 6.7 years, and a Levelized Cost of Electricity (LCOE) of $59/MWh, underscoring the system's financial viability. These findings demonstrate that the hybrid system offers a sustainable and efficient solution for power generation and waste heat recovery, aligning with the broader goals of advancing renewable energy technologies and setting a new benchmark in hybrid energy system design and optimization.

Environmental Diagnosis through a Flow Cytometric Approach.

In an era when ecological and environmental needs and responsibilities apply pressure on the world's countries and sustainability takes centre stage, ecologic/environmental (E/E) laboratories stand as beacons of scientific inquiry, innovating, optimising, and applying various tests for a better knowledge of our natural resources and the quality status of ecosystems. The purpose of this review is to provide an overview of the use of flow cytometry (FC) as a tool for assessing environmental quality, mainly using living organisms and their biological changes as bioindicators. Cytometric approaches applied to both marine and terrestrial ecosystems ensure the detection of biochemical and functional status of the cells composing either an organ thereof or the organism itself. In addition to cytometric evaluations of the biotic matrix, a brief overview of the techniques for the environmental assessment of biotic and abiotic matrices using mass spectrometry is given. The technique involving the continuous monitoring of the chemical and physical parameters of water, sediment, and soil is basically incapable of detecting any additive and synergetic effects of toxicants on living organisms. Therefore, techniques employing bioindicators provide valuable information for environmental diagnosis, and several studies have demonstrated the strong relationship between specific environmental data and cell/organ behaviour.

Advancement of Graphite-Clay Composite Electrodes via Different Compositions to Improve the Synergetic Matrix Effect Towards General Electroanalytical and Energy Storage Applications

Modern electrode technology trends for enhancing multifunctional electrodes, prioritizing energy storage and electroanalytical prospects. This study anticipates fabricating electrodes by incorporating cement and colloidal graphite, to improve the performance via synergetic interactions of the composite matrix. Graphite-montmorillonite-cement ternary composite electrode (GMMTCeCE) and graphite-colloidal graphite-montmorillonite-cement quaternary composite electrode (GCGMMTCeCE) are fabricated, as two types of electrodes. GMMTCeCE reflects the lowest peak-to-peak separation in Ce3+/Ce4+ (0.098 V), greater sensitivity towards [Fe(CN)6]4- (2.68 A·m·mol-1) and [Fe(CN)6]3- (2.64 A·m·mol-1), showing comparatively better performance in analyte detection than GCGMMTCeCE. Multilayered polyaniline (PANI) nanofibers network, which is unique in GMMTCeCE electropolymerization, accounts for very low serial (0.38 Ω) and charge transfer (0.59 Ω) resistances, while densely packed nanofibers of PANI in GCGMMTCeCE is responsible for the lowest ohmic resistance (1.31 Ω). Supercapacitor device fabricated by PANI-GMMTCeCE, achieved higher capacitance (1,002 F·g-1 at 5 mV·s-1) and showed greater cyclic stability, in contrast to relatively lower specific capacitance (685 F·g-1 at 5 mV·s-1) attained by PANI-GCGMMTCeCE, demonstrates the superiority of the supercapacitor of GMMTCeCE over GCGMMTCeCE for energy-storage purposes. Therefore, GMMTCeCE outperformed GCGMMTCeCE in electroanalysis and energy storage, confirming better synergetic interactions of the ternary composite matrix over the quaternary one. Besides, further improvements in graphite-clay composite matrix properties facilitate the advancement of electrochemical sensors and supercapacitor devices.

Synergetic effect of iron and tungsten on molybdenum‐doped HZSM‐5 zeolite in catalytic methane dehydroaromatization

AbstractMethane dehydroaromatization is a viable route for production of carbon and valuable petrochemicals. Unlike Fischer–Tropsch and methanol synthesis processes which have been scaled up to commercial level, development of methane dehydroaromatization to commercial level has been hampered by various challenges. In this work, a 5.4 wt. % trimetallic (Fe‐W‐Mo/HZSM‐5) catalyst has been synthesized, characterized, and applied in catalytic methane dehydroaromatization reaction. A gas chromatograph was used to analyze both liquid and gaseous products from the reactor. Based on 0.0013 moles of reacted methane after 240 min time on stream at 750, GHSV 960 mlg‐1cath‐1, and atmospheric pressure, a 5.4% Mo/HZSM‐5 catalyst recorded 7.9% methane conversion, 10.6% C2 hydrocarbon selectivity, 51.8% benzene selectivity, 9.8% toluene selectivity and 27.8% coke selectivity. Doping Mo/HZSM‐5 with Fe reduced methane conversion by 4.0%, increased C2 hydrocarbon selectivity by 1.7%, reduced benzene selectivity by 6.2% and increased toluene and coke selectivity by 1.8% and 2.8% respectively. Doping Mo/HZSM‐5 with W increased methane conversion by 7.3%, reduced C2 hydrocarbon selectivity by 2.1%, reduced benzene selectivity by 7.6% and increased toluene and coke selectivity by 0.3% and 9.4% respectively. When iron and tungsten were loaded onto Mo/HZSM‐5, catalytic activity of the tri‐metallic catalyst in methane conversion reduced by 2.0%, C2 hydrocarbon selectivity increased by 2.7%, benzene selectivity reduced by 3.1%, toluene selectivity reduced by 3.7%, and coke selectivity increased by 4.1%. Therefore, this present work demonstrates that metal synergy in a tri‐metallic catalyst plays a role in methane conversion and selectivity towards useful hydrocarbons.

Synergetic effects of tetracycline hydrochloride incorporated regenerated cellulose acetate - Bacterial cellulose hybrid nanocomposite: Potential in biomedical application

Litter from cigarette waste is a significant threat to organisms and ecosystems. However, this waste contains cellulose acetate (CA) that can be recycled into raw materials. In this study, recycled CA from cigarettes (CFCA) electrospun through electro-spinning technique and developed hybrid nanocomposite by incorporating CFCA in the fermentation media, followed by self-assembly of bacterial cellulose (BC). CFCA exhibit excessive hydrophobicity due to their high crystallinity and reorientation of hydrophobic groups. We aimed to improve the hydrophilic, thermal and mechanical properties of CFCA. We examined fiber morphology using a scanning electron microscope (SEM), Fourier Transform Infrared Spectroscopy (FTIR), X-ray Diffraction Analysis (XRD), thermogravimetric analysis (TGA), swelling capacity and mechanical properties. BC/CFCA showed higher swelling capacity, improved thermal properties, and good tensile strength compared to CFCA. Additionally, tetracycline hydrochloride (TC) was loaded into developed BC/CFCA matrix and evaluated in-vitro drug release, antibacterial activity and cytotoxicity. In-vitro drug release results showed that developed BC/CFCA can able to control TC release. In addition, prepared BC/CFCA-TC composites demonstrated excellent antibacterial activity against gram-positive and gram-negative bacteria. More importantly, BC/CFCA-TC composites exhibit good cytotoxicity on mouse fibroblast cells (L929). These characteristics of BC/CFCA-TC membranes indicate they may successfully serve as wound dressings and other medical biomaterials.

Graphene, graphene oxide or modified graphene in polyaniline based nanocomposites—features and technical highlights

Polyaniline is a remarkable conjugated polymer having valuable structural and physical characteristics. Nevertheless, polyaniline has poor solubility and structural durability which had limited its practical utilization. Consequently, polyaniline has been reinforced with carbonaceous and inorganic nanoparticles to enhance its processability and physical properties, such as electrical/thermal conductivity and thermal/mechanical stability. Accordingly, polyaniline has been applied as a valuable matrix material to form nanocomposites with graphene which is a one atom thick nanosheet of hexagonally arranged carbon atoms. Subsequently, graphene as well as modified graphene forms have been utilized as important nanoadditives for the polyaniline matrix. This state-of-the-art review article has been designed to investigate the fabrication, characteristics, and applications of the polyaniline and graphene/modified graphene based nanomaterials. Potential enhancements in the physical characteristics of the pristine polyaniline upon graphene reinforcement seemed to be reliant upon the matrix-nanofiller interactions, interface formation, and synergetic effects between polyaniline-graphene. Subsequently, practical aspects of the polyaniline/graphene nanocomposites have been discussed regarding their applications in the fields of solar cells, supercapacitors, and sensors. According to the literature analysis, dye sensitized solar cell based on polyaniline/graphene and polyaniline/graphene oxide exhibited superior power conversion efficiencies ∼2.0-7.6 % and open circuit voltage ∼500-800 mV. Supercapacitor electrodes based on polyaniline/graphene oxide and polyaniline/reduced graphene oxide showed significantly high values of specific capacitance and capacitance retention of ∼1100-1900 Fg−1 and ∼80-98 %, respectively, during >5000-6000 cycles. Besides, the polyaniline/graphene oxide depicted superior sensitivity and response time for gas sensors (∼20 % and 50 s, respectively) and humidity sensors (>90 % and 4-7 s, respectively) and low detection limits for biosensors.

Co-pyrolysis of plastic waste and macroalgae Ulva lactuca, a sustainable valorization approach towards the production of bio-oil and biochar

To address the pressing demand for sustainable energy in light of environmental challenges, this study explored the synergetic effects of the co-pyrolysis of polyethylene terephthalate (PET) and Ulva lactuca macroalgae to yield bio-oil and biochar. The objective is to enhance the bio-oil quality for wider usability and to combat marine pollution. By employing co-pyrolysis, notable progress has been achieved in bio-oil yield and quality, particularly in hydrocarbon content, through the integration of PET. The highest bio-oil yield of 37.91 % was achieved under optimal conditions at 500 °C with a feedstock mixture consisting of 40 % U. lactuca and 60 % PET. Under these conditions, the bio-oil exhibited a significant increase in hydrocarbon content, reaching 57.16 %, which is essential for improving its energy potential. Biochar quality was also enhanced, with the biochar from a 70 % U. lactuca and 30 % PET blend showing a BET surface area of 20.18 m2/g, compared to the initial 1.38 m2/g of raw U. lactuca, indicating improved surface properties. This study presents a sustainable energy generation and environmental preservation approach, underscoring the potential of synergistically utilizing marine resources and plastic waste.

A synergetic effect of light and anion: near-infrared colorimetric monitoring of nitric oxide (NO) release from fluoride/cyanide anions and a water responsive ruthenium nitrosyl complex.

Near-infrared (NIR) spectral-responsive multitasking chemical systems are always advantageous in biological and environmental systems. Although ruthenium complexes are highly attractive compounds for many applications, studies on NIR optical responsive sensors are very limited because of their synthetic difficulties. The sensing of fluoride and cyanide ions using ruthenium nitrosyl complexes is not known. In this study, we report the synthesis and characterization of a new terpyridine-based ruthenium nitrosyl complex [Ru(Cl)2NO(terpy-C6H4OH)] 1·Ru-OH. The complex exhibited distinct NIR absorptions at 680 nm, as well as a visible color change with the fluoride ion in DMSO-CH3CN medium. However, when the solvent is changed to DMSO-H2O, it responds only with a cyanide ion with a distinct colorimetric change. Binding of the F- ion leads to deprotonation of 1·Ru-OH; the deprotonated complex is also used for the colorimetric detection of a trace amount of water in DMSO and acetonitrile with a limit of detection (LOD) of 0.034 wt% and 0.007 wt%, respectively. Ruthenium nitrosyl complexes have appeared as promising platforms for light-controlled release of nitric oxide (NO), which can be beneficial for therapeutic application. NO release studies of 1·Ru-OH by UV-vis and FT-IR spectroscopy confirm that it can release NO in a light-controlled manner. In addition, the NO release could be monitored by the naked eye with a color change and spectral change in the NIR region. Importantly, NO release studies revealed that the rate of NO release could be modulated in the presence of the F- ion. Here, the fluoride ion acts as an allosteric regulator. These results demonstrate that 1·Ru-OH is both a promising multitasking colorimetric and NIR sensor and a colorimetric responsive NO-releasing agent.

RNA Nanotechnology for Codelivering High-Payload Nucleoside Analogs to Cancer with a Synergetic Effect.

Nucleoside analogs are potent inhibitors for cancer treatment, but the main obstacles to their application in humans are their toxicity, nonspecificity, and lack of targeted delivery tools. Here, we report the use of RNA four-way junctions (4WJs) to deliver two nucleoside analogs, floxuridine (FUDR) and gemcitabine (GEM), with high payloads through routine and simple solid-state RNA synthesis and nanoparticle assembly. The design of RNA nanotechnology for the co-delivery of nucleoside analogs and the chemotherapeutic drug paclitaxel (PTX) resulted in synergistic effects and high efficacy in the treatment of Triple-Negative Breast Cancer (TNBC). The 4WJ-drug complexes were confirmed to have efficient tumor spontaneous targeting and no toxicity because the motility of RNA nanoparticles has been previously shown to enable these RNA-drug complexes to spontaneously accumulate in tumor blood vessels. The negative charge of RNA enables those RNA complexes that are not targeted to tumor vasculature to circulate in the blood and enter the urine through the kidney glomerulus, without accumulating in organs, therefore being nontoxic. Drug incorporation into RNA 4WJ can be precisely controlled with a defined loading amount, location, and ratio. The incorporation of nucleoside analogs into 4WJ only requires one step using nucleoside analogue phosphoramidites during solid-phase RNA synthesis, without the need for additional conjugation and purification processes.

Synergetic effect of hybrid surface treatment on the mechanical properties of adhesively bonded AA2024-T3 joints

ABSTRACT Improving the surface properties of AA2024-T3 aluminium alloys is crucial for achieving durable and sustainable joints. For this purpose, AA2024-T3 alloys were first sandblasted at 4, 5 and 6 bar pressures using aluminium oxide and glass sphere abrasives. Then, the sandblasted samples were subjected to the chemical surface treatment resulting in a hybrid surface process. The surface properties of sandblasted and hybrid surface-treated AA2024-T3 alloys were characterised by 3D image analysis, contact angle and roughness measurement. Additionally, single-lap joints were fabricated using adhesives with low and high viscosity. The effect of changes in the viscosity of adhesives and the surface properties of the AA2024-T3 on the mechanical properties of the joints has been analysed in detail. It was found that both sandblasting and hybrid surface treatments applied to AA2024-T3 alloys caused significant improvement in the mechanical properties of the joints. AA2024-T3 alloys, which were chemically surface treated after being sandblasted with glass spheres at 6 bar pressure, were joined using low and high viscosity adhesives, and the failure load of these joints increased by approximately 110% and 68%, respectively, compared to untreated samples. In the case of aluminium oxide usage, the increase rates were determined to be 93% and 43%.

Synergistic effect and role of light for efficient photothermocatalytic CO2 reduction by CH4 on Pd/Co-Al1Mg3Ox

Photothermocatalytic CO2 reduction by CH4 converts greenhouse gases into valuable syngas, but limited by high light intensity and carbon deposition. Here, we designed a nanocomposite supporting low content of Pd nanoparticles on Co and Al doped MgO (Pd/Co-Al1Mg3Ox), achieving high production rates of H2 (rH2, 73.04 mmol min−1 g−1) and CO (rCO, 84.80 mmol min−1 g−1) with light-to-fuel efficiency (η, 25.3 %) at relatively low light intensity (81.1 kW m−2). Compared to Pd/Al1Mg3Ox, Pd/Co-Al1Mg3Ox demonstrates improvements of rH2, rCO and η by 6.5, 6.2 and 6.7 times respectively with great durability of 48 hours. This originates from a synergetic effect between Pd and Co-Al1Mg3Ox that the participation of active oxygen from Co-Al1Mg3Ox greatly accelerates carbon species (C*) oxidation. Interestingly, light plays unique roles on Pd/Co-Al1Mg3Ox which not only expedites C* oxidation, activates the oxygen connected to Pd and Co-Al1Mg3Ox, but also reverses rapid thermocatalytic deactivation by boosting CO desorption.

Synergetic effect of bioglass and nano montmorillonite on 3D printed nanocomposite of polycaprolactone/gelatin in the fabrication of bone scaffolds

Nowadays, bone injuries and disorders have increased all over the world and can reduce the quality of human life. Bone tissue engineering repair approaches require new biomaterials and methods to construct scaffolds with the required structural properties as well as improved performance. As potential therapeutic strategies in bone tissue engineering, 3D printed scaffolds have been developed. Polycaprolactone/Ceramic composites have attracted considerable attention due to their cytocompatibility, biodegradability, and physical properties. In this study, a 3D printing process was used to create polycaprolactone (PCL)-Gelatin (GEL) scaffolds containing varying concentrations of Bioglass (BG) and Nano Montmorillonite (MMT). This mixture was then loaded into a 3D printer, and the scaffolds were printed layer by layer. After constructing the scaffolds, they were then examined for their physical, chemical, and biological characteristics. Surface appearance was analyzed with a scanning electron microscope (SEM), which revealed that NC increased the diameter of pores from 465 to 480 μm. The elements in the scaffolds were evaluated by EDX analysis, and a uniform dispersion of nano montmorillonite particles was observed. The compressive strength reached 76.43 MPa for PCL/G/35 %MMT/15 %BG scaffold. Also, the rate of water absorption, biodegradability and bioactivity of PCL-GEL scaffolds increased significantly in the presence of NC. According to the MTT cell test results, adding BG and NC increased cell proliferation, adhesion and cell viability to 127.7 %. These findings indicated that the 3D printed PCL/G/35 %MMT/15 %BG scaffold has promising strategies for bone repair applications. Also, polynomial curve fitting shows that scaffold degradability after soaking in PBS can be predicted using the initial weight and soaking time. Adding more variables and data could improve prediction accuracy, reducing the need for experiments and conserving resources.

Modulating effects of fodder grasses extracts on antibiotic sensitivity and biofilm production in avian pathogenic Escherichia coli strains

Extracts of certain fodder grasses may be viewed as powerful agents against infections induced by avian pathogenic Escherichia coli strains. Here we demonstrated ability of Galega orientalis and Rhaponticum carthamoides extracts, alone or in combination with antibiotics, to inhibit growth, viability and biofilm formation in avian pathogenic Escherichia coli strains with different sensitivity to antibiotics and non-pathogenic laboratory strain E. coli BW25113 as well as its mutant derivatives. Modulation of motility and production of extracellular structures in the presence of the extracts correlated with their anti-biofilm effects. Interestingly, an increase in antibacterial action of kanamycin, streptomycin, ciprofloxacin, and cefotaxime on both biofilms and planktonic cultures of the studied strains was observed in the presence of the extracts, including antibiotic resistant APEC strain #45. The extracts alone showed weak prooxidant activity which could contribute to modification of redox-sensitive sites of various regulatory circuits, resulting to synergetic effects in combination with antibiotics.

Photoactivated Hydrogel Therapeutic System with MXene-Based Nanoarchitectonics Potentiates Endogenous Bone Repair Through Reshaping the Osteo-Vascularization Network.

The repair and reconstruction of large-scale bone defects face enormous challenges because of the failure to reconstruct the osteo-vascularization network. Herein, a near-infrared (NIR) light-responsive hydrogel system is reported to achieve programmed tissue repair and regeneration through the synergetic effects of on-demand drug delivery and mild heat stimulation. The spatiotemporal hydrogel system (HG/MPa) composed of polydopamine-coated Ti3C2Tx MXene (MP) nanosheets decorated with acidic fibroblast growth factor (aFGF, a potent angiogenic drug) and hydroxypropyl chitosan/gelatin (HG) hydrogel is developed to orchestrate the reconstruction of the osteo-vascularization network and boost bone regeneration. Upon exposure to NIR light irradiation, the engineered HG/MPa hydrogel can achieve the initial complete release of aFGF to induce rapid angiogenesis and provide sufficient blood supply, maximizing its biofunction in the defect area. This integrated hydrogel system demonstrated good therapeutic efficacy in promoting cell adhesion, proliferation, migration, angiogenesis, and osteogenic differentiation through periodic NIR irradiation. In vivo, animal experiments further revealed that the spatiotemporalized hydrogel platform synergized with mild photothermal treatment significantly accelerated critical-sized bone defect healing by increasing the osteo-vascularization network density, recruiting endogenous stem cells, and facilitating the production of osteogenesis/angiogenesis-related factors. Overall, smart-responsive hydrogel couldenhance the reconstruction of the osteo-vascularization network in bone regeneration.

Fabrication of Hierarchical Nanostructures featuring Amplified Asymmetry through Co‐assembly of Liquid Crystalline Block Copolymer and Chiral Amphiphiles

The widespread presence of hierarchical asymmetric structures in nature has sparked considerable interest because of their unique functionalities. These ingenious structures across multiple scales often emerge from the transfer and amplification of asymmetry from chiral molecules under various synergistic effects. However, constructing artificial chiral asymmetric structures, particularly in developing hierarchical multicomponent structures analogous to those formed in nature through synergistic non‐covalent interactions, still presents tremendous challenges. Herein, we propose a co‐assembly strategy to fabricate hierarchical chiral mesostructures by combining a liquid crystalline block copolymer (LC‐BCP) with a small molecular amphiphile containing chiral alanine or phenylalanine as a linker. Through a classic solvent‐exchange process, chiral amphiphiles embedded within LC‐BCP finely regulate the LC ordering effect and facilitate transfer and amplification of asymmetry. Consequently, various co‐assembled structures with significant hierarchical chirality features are obtained through synergetic effects. Remarkably, subtle alterations to the side groups of amino acids in the amphiphiles effectively adjust the hierarchical morphology transition. Moreover, the covalent bonding sequence of amino acids in the amphiphiles emerges as a critical factor governing the formation of hierarchical nanofibers and multilayered vesicles exhibiting a superhelical sense.

Fabrication of Hierarchical Nanostructures Featuring Amplified Asymmetry Through Co-Assembly of Liquid Crystalline Block Copolymer and Chiral Amphiphiles.

The widespread presence of hierarchical asymmetric structures in nature has sparked considerable interest because of their unique functionalities. These ingenious structures across multiple scales often emerge from the transfer and amplification of asymmetry from chiral molecules under various synergistic effects. However, constructing artificial chiral asymmetric structures, particularly in developing hierarchical multicomponent structures analogous to those formed in nature through synergistic non-covalent interactions, still presents tremendous challenges. Herein, we propose a co-assembly strategy to fabricate hierarchical chiral mesostructures by combining a liquid crystalline block copolymer (LC-BCP) with a small molecular amphiphile containing chiral alanine or phenylalanine as a linker. Through a classic solvent-exchange process, chiral amphiphiles embedded within LC-BCP finely regulate the LC ordering effect and facilitate transfer and amplification of asymmetry. Consequently, various co-assembled structures with significant hierarchical chirality features are obtained through synergetic effects. Remarkably, subtle alterations to the side groups of amino acids in the amphiphiles effectively adjust the hierarchical morphology transition. Moreover, the covalent bonding sequence of amino acids in the amphiphiles emerges as a critical factor governing the formation of hierarchical nanofibers and multilayered vesicles exhibiting a superhelical sense.

Synergetic effect of Fe decorated MnO2 nanocatalyst application in propane and benzyl alcohol oxidation

In heterogeneous catalysis, one of the key challenges is to develop inexpensive and abundant materials. Herein, spherically shaped α–Fe2O3 nanoparticles decorated over MnO2 nanorods surface (Fe/MnO2NRs) was synthesized via hydrothermal followed by co–precipitation methods. Experimental results indicated that the inclusion of Fe in MnO2NRs promotes a strong interaction that increases the reducibility of Mn4+ to Mn3+ and surface adsorbed oxygen (Oads.), which in turn increases the activation of surface oxygen on MnO2NRs. The 10 wt% Fe–loaded catalyst (10Fe/MnO2NRs) exhibited the highest catalytic activity. It was observed that oxidizing 10 % (T10), 50 % (T50), and 90 % (T90) of propane required temperatures of 140 °C, 180 °C, and 220 °C, respectively. This catalyst showed stability in H2O atmospheres and apparent activation energy as low as 52.54 kJ mol−1. In addition, the vapour phase oxidation of benzyl alcohol (BnOH) over different Fe–loaded MnO2NRs catalysts is investigated. The rate of BnOH oxidation over 10Fe/MnO2NRs catalyst is 1.71 times greater than bare MnO2NRs at 240 °C. The increased oxygen vacancies can improve the oxidation activity of propane and BnOH by facilitating the adsorption and activation of O2 to produce reactive oxygen species. This work offers a novel approach to increase manganese oxides surface oxygen activity, which can be used to create efficient catalysts for the low–temperature decomposition of volatile organic compounds (VOCs) and other organic functional group transformations via oxidation reaction.

Advanced Fuel Based on Semi-Coke and Cedarwood: Kinetic Characteristics and Synergetic Effects

Advanced Fuel Based on Semi-Coke and Cedarwood: Kinetic Characteristics and Synergetic Effects

Oxidation mechanism of sulfur-containing compounds and antioxidant depletion dynamics: Insights into interactions

Sulfur-containing compounds (SCCs) are the most abundant heteroatomic organic species (HOS) in petroleum fuels. This study investigates the dynamics of SCCs in surrogate fuel systems, focusing on their oxidation stability, reactivity, and interactions. An analysis of eleven selected SCCs, spanning both reactive (thiols, sulfides, and disulfides) and nonreactive (thiophenes and benzothiazole) species, was conducted at 140 °C. The investigation delves into reaction and degradation mechanisms, exploring resulting products, binary mixtures of reactive SCCs for potential interactions, and multicomponent SCC systems to understand nuanced interaction. Findings reveal unique reaction pathways in single-component SCCs, synergetic and antagonistic effects in binary mixtures, and substantial decreases in reaction rates in all multicomponent systems. Moreover, SCCs expedited antioxidant consumption, highlighting their pivotal role in fuel stability and degradation. The study contributes valuable insights into SCC dynamics, advocating further exploration of HOS’s interactions for enhanced fuel formulation and stability testing strategies.