Incomplete Reaction Research Articles

A novel neutralization process for improving dehydration performance of industrial by-product gypsum

By-product gypsum, produced through the traditional neutralization precipitation method for treating industrial acidic wastewater, is difficult to recycle due to its high moisture content. In this study, we proposed a novel neutralization process i.e. the two-stage neutralization method. By-product gypsum was used as an alkaline neutralizer and recycled as seed crystals for the first time. The original by-product gypsum has the poor dehydration performance due to its small particle size and the presence of colloids on its surface. After adding the by-product gypsum to the acidic wastewater, the ratio of CaO/SO3 in the system descended and colloids were dissociated. On the one hand, the alkaline component of the incomplete reaction continues to play a neutralizing role. On the other hand, CaSO4·2H2O particles act as seed crystals, promoting rapid growth of new crystals along their surface, which effectively improved crystallization performance and dehydration performance of the neutralization slag (outward discharge of slag). Compared with the original method, the wet weight of the neutralization slag is decreased from 186.0 g/L to 88.8 g/L, and the water cut is declined from 64.5% to 34.1%. The utilization ratio of the carbide slag augmented from 63.0% to 99.47%.

Experimental and numerical study on vented H2/air explosion in an obstructed duct: Effects of hydrogen concentration and vent size

In this study, the effects of hydrogen concentration (C) and vent size (AV) on the vented H2/air explosion in an obstructed duct were investigated using experimental methods and FLACS simulation software at an initial pressure and temperature of 101 kPa and 291K, respectively. A vent coefficient KA is chosen to represent AV to illustrate its influence on the explosion venting of H2/air. The results demonstrate that the maximum internal overpressure (pmax) and the maximum external overpressure (pext) increase and then decrease with C increasing from 10% to 60%. The highest pmax and pext are reached at C = 35% in experiments, but achieved at C = 30% in simulations because incomplete chemical reactions were not taken into account. In the tests with C <50%, the flame evolution inside the duct includes five stages: spherical flame, elliptical flame, finger-shaped flame, near-planar flame, and tulip-shaped flame. No tulip flame is observed for C ≥50%. FLACS can simulate the flame structure evolution for various C, but it cannot accurately simulate the flame propagation speed. FLACS overestimates the flame propagation speed in the tests with C ≤25%, but underestimates the flame propagation speed for C ≥35%. Under the initial condition of C = 15%, the above-mentioned five stages of flame evolution can be simulated by FLACS for KA ≤0.4; however, neither the near-plane nor tulip flame is observed in simulations for KA >0.4.

Sintering Behavior and Mechanical Properties of Ti–TiBw Composites Prepared with Pre‐alloyed Ti–TiBw Composite Powders

Prealloyed powders present a promising alternative to traditional ball milling processes in powder metallurgy, addressing challenges such as uneven powder mixing and incomplete reinforcement reactions. This study investigates the preparation of Ti–TiBw composites using spark plasma sintering (SPS) at temperatures ranging from 950 to 1050 °C, utilizing Ti–TiBw prealloyed composite powders. The effects of sintering temperature on the microstructure and mechanical properties of Ti–TiBw composites are studied, comparing prealloyed composite powders with ball‐milled premixed powders. As a result, the composites exhibit excellent strength and ductility, with an ultimate tensile strength of 676 MPa at 1000 °C and an elongation of 20.42% at 1050 °C. Comparatively, Ti–TiBw composites prepared from premixed powders achieve densification at 1050 °C, 50 °C higher than those prepared from prealloyed powders.

Structural modulation of Na4Fe3(PO4)2P2O7 via cation engineering towards high-rate and long-cycling sodium-ion batteries

Mixed iron-based phosphate Na4Fe3(PO4)2P2O7/C (NFPP) has gradually emerged as a promising cathode material for sodium-ion batteries (SIBs) owing to its affordability and convenient preparation. However, poor electrical conductivity and inadequate sodium-ion diffusion limit the exertion of its electrochemical properties. Herein, a structural modulation strategy based on Cd doping is applied to NFPP to address the above limitations. In situ X-ray diffraction analysis reveals that Cd-doped NFPP (NFCPP) undergoes an incomplete solid-solution reaction driven by Fe2+/Fe3+ redox. Cd doping effectively stabilises the crystal structure, resulting in a minimal 1 % change in unit cell volume during cycling. Density of state calculations indicate that Cd doping reduces the band gap, increases the local electron density and significantly improves electron conductivity. Benefitting from the enhanced electrochemical kinetics and intercalation pseudocapacitance, the optimised Na4Fe2.91Cd0.09(PO4)2P2O7/C (NFCPP@3%) exhibits exceptional rate performance (capacity of 62 mAh/g at 20 C) and ultra-long cycling life (82.7 % after 6000 cycles at 20 C). A full SIB prepared using NFCPP@3% and hard carbon, display a 91 % capacity retention rate at a current density of 130 mA g−1 over 200 cycles. This work demonstrates that doping can effectively enhance electrochemical performance and offers insights into future development of SIBs.

Beyond Catalysts: Pioneering a New Era in Aluminum‐Based Electrochemical Energy Systems

AbstractAqueous Aluminum‐air batteries (AABs) hold promise for advancing high‐energy density storage systems in future technologies. However, their widespread practical deployment is limited by the inherent hydrogen side reactions in Aluminum (Al) and incomplete cathodic reactions. To address these challenges, the Al‐sodium persulfate (Na2S2O8) system is introduced as an alternative to traditional AABs. Utilizing Na2S2O8 allows to simultaneously achieve three critical objectives, namely, eliminating the need for a cathode catalyst, increasing the system voltage from 1.4 to 2 V, and reducing the hydrogen evolution reaction (HER). Three distinct configurations of the Aluminum electrochemical energy system (Al‐EES) using Na2S2O8: static, flow, and gel are developed. The static configuration demonstrates a performance 1.7 times superior to that of traditional AABs. The flow configuration of Al‐EES achieves a discharge duration of 77 h, which is three to four times longer than that of AABs and exhibits an energy density of 2,650 Wh kgAl−1. This emerging technology has the potential to significantly enhance electric vehicles by providing powerful, efficient, cost‐effective, and durable power‐generation devices.

Basic oxygen furnace (BOF) slag as an additive in sodium carbonate-activated slag cements

Basic oxygen furnace slag (BOFS) is a high-volume waste resulting from the production of steel from pig iron. Due to its high free lime content, BOFS is difficult to recycle and/or include into conventional cement systems. Alkali-activation technology offers a pathway to transform industrial wastes such as BOFS into low-carbon cements. Alternative precursors for cement systems are needed as the reliance on commonly used materials like ground granulated blast furnace slag (GGBFS) is becoming unsustainable due to decreasing availability. This study investigates alkali-activated cements incorporating 20 and 30 wt.% of naturally weathered BOFS as a replacement for GGBFS, in both sodium silicate- and sodium carbonate-activated systems. A fraction of BOFS subject to mechanical activation is compared against the untreated BOFS in the 20 wt.% systems. It is observed that in naturally weathered BOFS, a significant portion of the free-lime is found to convert to portlandite, which accelerates alkali-activation kinetics. In sodium silicate-activated systems, the high pH of the activator results in incomplete reaction of the portlandite present in BOFS. The sodium carbonate-activated system shows near complete conversion of portlandite, causing an acceleration in the kinetics of reaction, setting, and hardening. These findings confirm the viability of sodium carbonate activated GGBFS-based systems with only a minor loss in strength properties. BOFS can be utilised as a valuable cement additive for the production of sustainable alkali-activated cements utilising sodium carbonate as a less carbon-intensive activator solution than the more commonly used sodium silicate. Mechanical activation of BOFS offers further optimisation potential for alkali-activation.

Explosion characteristics of AlH3 dust cloud with varying micron particle sizes

The explosion characteristics of AlH3 dust clouds with varying micron particle sizes are investigated in this paper. The explosion mechanism of AlH3 dust clouds is initially explored. The results indicate that the activation energy for hydrogen evolution shows an increasing trend with the AlH3 particle size, and both of these values are comparable to the 30 kJ/mol desorption energy of hydrogen from large AlH3 clusters. Due to the rapid dehydrogenation rate and small-size residual aluminum core, fine AlH3 particles exhibit a continuous gas-phase flame and fast propagation velocity. With increasing particle size, the lower dehydrogenation rate, reduced specific surface area, and higher volume heat capacity contribute to a higher level of incomplete reaction. Consequently, large micro-sized AlH3 particles display a discrete flame, slower flame velocity, and lower explosion pressure. The flame delamination phenomenon is not observed in our experiments on AlH3 dust clouds.

Flame characteristics and NO emission behaviors of methane/ammonia counterflow premixed flames with opposed N2 or air stream

Behaviors of methane/ammonia counterflow premixed flames and NO emission are numerically and experimentally investigated with opposed N2 or air stream by varying strain rate (ag) and equivalence ratio (ϕ). The premixed stream is 80% methane and 20% ammonia by volume mixed with air considering the utilization of ammonia by blending hydrocarbon fuels. The opposed stream is either N2 or air considering the potential application in gas turbines having single- or two-stage combustion. The simulations are conducted by increasing ag up to flame extinction for a specified ϕ and an experiment is conducted to evaluate various kinetic mechanisms. The extinction strain rate increases monotonically with ϕ with opposed air stream (AS), while increases and then decreases with opposed nitrogen stream (NS). The extinction mechanisms are explained by adopting the concepts of the local equilibrium temperature and heat loss ratio. For lean and rich mixtures with NS and lean mixtures with AS, the extinction occurs due to comparable effects of incomplete reaction and heat loss from the flame to the downstream burnt region. While for rich mixtures with AS, the extinction is attributed mainly to incomplete reaction. The contribution of thermal NO as compared with prompt NO in NO production is weak for all cases with NS and AS. The emission index (EINO) for lean and rich mixtures with NS and for lean mixtures with AS decreases monotonically with the increase of strain rate for all ϕ. Increasing equivalence ratio at a specified ag decreases NO production for lean and rich mixtures with NS and lean mixtures with AS. While for rich mixtures with AS, the EINO increases monotonically with ag. From the reaction pathway analysis, for lean mixtures, the effect of increasing ag on the reduction of NO production is attributed by weakening NH-related reaction paths, while NH2-related reaction paths change little. When ϕ increases for a specified ag with NS, NO production is reduced by weakening NH2-related reaction paths and strengthening NH-related reaction paths. For rich mixtures with AS, increasing ag increases NO production by strengthening NH2-related reaction paths.

Changes in the state of matter of KCIO4 to improve thermal and combustion properties of Al/MoO3 nanothermite

To improve the thermal and combustion properties of nanothermites, a design theory of changing the state of matter and structural state of the reactants during reaction was proposed. The Al/MoO3/KClO4 (Kp) nanothermite was prepared and the Al/MoO3 nanothermite was used as a control. SEM and XRD were used to characterize the nanothermites; DSC was used to test thermal properties; and constant volume and open combustion tests were performed to examine their combustion performance. Phase and morphology characterization of the combustion products were performed to reveal the mechanism of the aluminothermic reaction. The results show that the Al/MoO3/Kp nanothermite exhibited excellent thermal properties, with a total heat release of 1976 J·g− 1, increasing by approximately 33% of 1486 J·g− 1 of the Al/MoO3 nanothermite, and activation energy of 269.66 kJ·mol− 1, which demonstrated higher stability than the Al/MoO3 nanothermite (205.64 kJ·mol− 1). During the combustion test, the peak pressure of the Al/MoO3/Kp nanothermite was 0.751 MPa, and the average pressure rise rate was 25.03 MPa·s− 1, much higher than 0.188 MPa and 6.27 MPa·s− 1 of the Al/MoO3 nanothermite. The combustion products of Al/MoO3 nanothermite were Al2O3, MoO, and Mo, indicating insufficient combustion and incomplete reaction, whereas, the combustion products of Al/MoO3/Kp nanothermite were Al2O3, MoO, and KCl, indicating complete reaction. Their “coral-like” morphology was the effect of reactants solidifying after melting during the combustion process. The characterization of reactants and pressure test during combustion reveals the three stages of aluminothermic reaction in thermites. The excellent thermal and combustion performance of Al/MoO3/Kp nanothermite is attributed to the melt and decomposition of Kp into O2 in the third stage. This study provides new ideas and guidance for the design of high-performance nanothermites.

AviTrap: A novel solution to achieve complete biotinylation.

Site specific biotinylation of AviTagged recombinant proteins using BirA enzyme is a widely used protein labeling technology. However, due to the incomplete biotinylation reactions and the lack of a purification method specific for the biotinylated proteins, it is challenging to purify the biotinylated sample when mixed with the non-biotinylated byproduct. Here, we have developed a monoclonal antibody that specifically recognizes the non-biotinylated AviTag but not the biotinylated sequence. After a ten-minute incubation with the resin that is conjugated with the antibody, the non-biotinylated AviTagged protein is trapped on the resin while the fully biotinylated material freely passes through. Therefore, our AviTrap (anti-AviTag antibody conjugated resin) provides an efficient solution for enriching biotinylated AviTagged proteins via a simple one-step purification.

Understanding the charge transfer effects of single atoms for boosting the performance of Na-S batteries.

The effective flow of electrons through bulk electrodes is crucial for achieving high-performance batteries, although the poor conductivity of homocyclic sulfur molecules results in high barriers against the passage of electrons through electrode structures. This phenomenon causes incomplete reactions and the formation of metastable products. To enhance the performance of the electrode, it is important to place substitutable electrification units to accelerate the cleavage of sulfur molecules and increase the selectivity of stable products during charging and discharging. Herein, we develop a single-atom-charging strategy to address the electron transport issues in bulk sulfur electrodes. The establishment of the synergistic interaction between the adsorption model and electronic transfer helps us achieve a high level of selectivity towards the desirable short-chain sodium polysulfides during the practical battery test. These finding indicates that the atomic manganese sites have an enhanced ability to capture and donate electrons. Additionally, the charge transfer process facilitates the rearrangement of sodium ions, thereby accelerating the kinetics of the sodium ions through the electrostatic force. These combined effects improve pathway selectivity and conversion to stable products during the redox process, leading to superior electrochemical performance for room temperature sodium-sulfur batteries.

Passivating Defects via Retarding the Reaction Rate of FAI and PbI2 Enables Stable Perovskite Solar Cells.

The two-step sequential deposition strategy has garnered widespread usage in the fabrication of high-performance perovskite solar cells based on FAPbI3. However, the rapid reaction between FAI and PbI2 during preparation often leads to incomplete reactions, reducing the device efficiency and stability. Herein, we introduced a multifunctional additive, 2-thiophenyl trifluoroacetone (TTA), into the FAI precursor. The incorporation of TTA has proven to be highly effective in slowing the reaction rate between FAI and PbI2, resulting in increased perovskite formation and improved efficiency and stability of the devices. TTA's CF3 groups interact with FAI via hydrogen bonding, effectively suppressing FA+ defects. The S and C═O groups share lone pair electrons with uncoordinated Pb2+, leading to a reduction in perovskite film defects and suppressing nonradiative recombination. Additionally, the CF3 groups impart hydrophobicity, protecting the perovskite film from moisture-induced erosion. As a result, the TTA-modified perovskite film achieves a Champion efficiency of 23.42% compared to the control's 21.52, with 20.58% efficiency for a 25 cm2 solar module. Remarkably, the unencapsulated Champion device retains 86% of its initial PCE after 1080 h under dark conditions (60 ± 5 °C, 35 ± 5% RH), indicating enhanced long-term stability. These findings offer a promising and cost-effective tactic for high-quality perovskite film fabrication.

Completing and Balancing Database Excerpted Chemical Reactions with a Hybrid Mechanistic-Machine Learning Approach.

Computer-aided synthesis planning (CASP) development of reaction routes requires an understanding of complete reaction structures. However, most reactions in the current databases are missing reaction coparticipants. Although reaction prediction and atom mapping tools can predict major reaction participants and trace atom rearrangements in reactions, they fail to identify the missing molecules to complete reactions. This is because these approaches are data-driven models trained on the current reaction databases, which comprise incomplete reactions. In this work, a workflow was developed to tackle the reaction completion challenge. This includes a heuristic-based method to identify balanced reactions from reaction databases and complete some imbalanced reactions by adding candidate molecules. A machine learning masked language model (MLM) was trained to learn from simplified molecular input line entry system (SMILES) sentences of these completed reactions. The model predicted missing molecules for the incomplete reactions, a workflow analogous to predicting missing words in sentences. The model is promising for the prediction of small- and middle-sized missing molecules in incomplete reaction records. The workflow combining both the heuristic and machine learning methods completed more than half of the entire reaction space.

Mass yields of products and composition of syngas from pyrolysis of Brazilian plastic solid wastes: Combustion simulation and burner design to minimize COx and CxHy emissions

For the first time, the mass yields of products and the composition of synthesis gas (syngas) from pyrolysis of Brazilian plastic solid waste were evaluated for a reactor processing 20 g of plastic at 800 °C. Combustion of the syngas was simulated, evaluating the levels of COx and CxHy emissions, and a burner was designed to minimize emissions during combustion. The main findings highlighted the importance of performing thermogravimetric analyses of waste materials. Higher thermal degradation temperatures (530–900 °C) were obtained for all the plastics, compared to values reported in the literature (300–600 °C). Between 46.7 and 98.0 wt% of syngas was produced, with lower heating values ranging from 10390 to 45684 kJ kg−1, due to differences between the plastics in the fractions of inorganic and hydrocarbon gases produced. The maximum temperatures for syngas combustion, simulated using ANSYS software, were 2000 and 800 °C inside the burner and combustion chamber, respectively. In the burner, higher COx and CxHy levels were related to the syngas composition and incomplete chemical reactions in the flame zone. The CO and CxHy levels decreased towards the combustion chamber, where CO2 was less than 8 wt%, in compliance with the CONAMA 316/2002 regulation.

Thermochemical heat storage performance of Fe-doped MgO/Mg(OH)2: Experimental and DFT investigation

MgO/Mg(OH)2 thermochemical heat storage system can realize large-scale energy storage by repetitive hydration/dehydration reactions to enhance the stability of solar energy utilization. However, slow interconversion and incomplete reactions caused by agglomeration restrict the cyclic heat storage capability of MgO/Mg(OH)2. In this work, a low-cost efficient Fe-doped MgO was prepared by a simple wet-mixing method and its energy released performance and kinetics in MgO/Mg(OH)2 heat storage progress were examined in a twin fixed-bed reactor and a simultaneous thermal analyzer. Additionally, density functional theory calculations were used to examine the impact of Fe on the mechanisms of MgO/Mg(OH)2 heat storage process. The results shows that when the molar ratio of MgO to Fe is 95:5, the energy released density of Fe-doped MgO is about 400 % higher than that of MgO after 10 heat storage cycles. In preparation process, the existence of Fe leads to the generation of MgFe2O4, which forms layered microstructure with the high specific surface area and pore volume and mitigates agglomeration behavior of MgO. It improves the cyclic stability of MgO and reduces the dehydration temperature of Mg(OH)2, and simultaneously the activation energy of the dehydration stage is reduced by 33.2 %. Fe enhances the interaction of H2O with the MgO surface and promotes the dissociation of H2O on Mg(OH)2 surface. Combined with economic analysis, Fe-doped MgO is a suitable material for MgO/Mg(OH)2 heat storage cycles.

Construction of Al@PTFE composites with excellent ignition and combustion properties through mechanical and thermal activation

Fluorine-based aluminum thermite have excellent ignition and combustion properties. Nonetheless, its combustion kinetics and energy release are hindered by slow mass diffusion and incomplete reactions. Therefore, this study successfully prepared an Al@PTFE composite with a core-shell structure, utilizing mechanical activation and sintering techniques, to enhance combustion properties and energy release rate. SEM, XRD, FTIR and XPS characterization results demonstrate the unique core-shell structure of the samples and the homogeneous distribution of elements on the surface. In comparison to the physical mixture, the Al@PTFE composite exhibits significantly higher values for Pmax (2.19 times), Pmax/Δt (11.30 times), and flame propagation velocity (4.5 times). Furthermore, the combustion duration required to reach the maximum flame height was reduced by 131.75 ms. The adsorption, decomposition and reaction processes of PTFE on the surface of aluminum particles were demonstrated based on RMD simulations. The promotion mechanism of PTFE on combustion in aluminum particles was elucidated.

On the structure and dynamics of strong and weak eigenvalue detonation in condensed explosives

An eigenvalue detonation, also known as a pathological detonation, is a detonation with incomplete reaction at a point in the detonation reaction zone, that is sonic relative to the leading shock. Aluminized explosives are made by combining a molecular explosive with aluminum and other additives. During detonation, the molecular explosive’s first exothermic decomposition generates products that react exothermically with aluminum, but generate endothermic condensed oxide products, characteristic of eigenvalue detonation.We use a three-component model, for unreacted explosive, intermediate and final products, each with a simple ideal equation of state, and a simple depletion model for the reaction kinetics, with parameters representative of a typical aluminized explosive. We analyze the steady detonation structure in a state-variable, phase plane that allows clear identification of strong and weak eigenvalue detonation. We describe the striking contrast of the strong eigenvalue detonation with significantly higher pressure, density, and temperature in the reaction zone structure, than that of the weak eigenvalue detonation.The accessibility of the strong eigenvalue detonation branch is demonstrated by means of dynamic impact simulations. We present examples of initiation of detonation for reverse impact of unreacted explosive with a stationary wall, and finite thickness, inert flyer impact of unreacted explosive. A control volume analysis is used to describe the energy flow in the region between the incipient sonic point and the flyer explosive interface. This is followed by discussion and conclusions.

Deterioration of mechanical properties and damage mechanism of flue gas desulfurization gypsum backfill under long-term erosion of chloride salt solution

Flue gas desulfurization gypsum (FGDG), a solid waste material generated by power plants, offers a cost-effective solution for preparing backfill materials. Concurrently, given that most backfill materials are exposed to mine water erosion, an investigation into the mechanical performance degradation and damage mechanisms of FGDG backfill materials subjected to prolonged chloride salt erosion is crucial for ensuring the stability of goaf backfills (by goaf, we mean the area or space that remains underground after the extraction of valuable minerals). This study explores the mechanical properties and damage mechanisms of backfill samples treated with varying concentrations of chloride. The findings indicate that over time, the mass of the sample initially decreases, experiences a slight increase, and then gradually declines. Simultaneously, the strength and structure of the sample deteriorate rapidly, followed by a partial recovery. The rebound in sample mass is attributed to an incomplete hydration reaction that continuously transforms free water into bound water. Microstructure analysis techniques, such as X-ray diffraction (XRD) and field-emission scanning electron microscopy (FE-SEM), reveals that the degradation in mechanical strength and structure is a consequence of chloride salt erosion. Subsequent reuse is facilitated by the formation of Friedel's salt resulting from the reaction between hydration products and chloride ions, filling voids in the sample and impeding further chloride ion erosion into the deeper regions. Notably, FGDG exhibits outstanding reuse performance in prolonged and high-concentration chloride ion environments. This study serves as a reference for understanding the deterioration mechanism and practical application of backfills in chloride-rich environments.

EXPERIMENTAL RESEARCH ON MECHANICAL PROPERTIES OF MAGNESIUM OXYCHLORIDE-BASED TITANIUM GYPSUM CONCRETE

To alleviate the environmental pollution, waste of resources of titanium gypsum (TG) and the industrial residue from the production of titanium dioxide by sulfuric acid method, and to develop new building materials, the effects of different dosage on the strength and microscopic properties of magnesium oxychloride cement (MOC) were studied by methods such as unlimited compressive strength, scanning electron microscope (SEM) and X-ray diffractometer (XRD). Results show that the compressive strength of the samples increases first and then decreases with the increase of the amount of titanium gypsum. In the control group, when the dosage was 0%, the compressive strength of the samples was 40.37 MPa. The compressive strength is 34.29 MPa at 50% dosage, which is lower than the compressive strength of the control group by 15.06%. The internal structure changes, and there is an incomplete reaction of SiO2. The addition of titanium gypsum increases the ductility of concrete, but has little effect on its elastic modulus. Therefore, the proper inclusion of TG in the TG-MOC gelling material can improve its deformation ability and maintain a certain strength. This provides a useful reference and guidance for the application of magnesium oxychloride-based titanium gypsum in engineering practice. Keywords: Magnesium oxychloride cement, Titanium gypsum, Mechanical propertie, Microscopic analysis, Compressive strength.

Effect of excitation Strouhal number on a backward-inclined jet flame in crossflow

Combustion is often accompanied by environmental pollution due to incomplete reaction. A non-excited flame usually exhibits poor combustion performance with features of diffusion flame such as dual-peak temperature distributions and large combustion product concentrations. Efficient fuel-air mixing has been identified as a key factor in mitigating this issue. The present study investigated the effects of the acoustic excitation Strouhal number on the combustion performance of a backward-inclined jet flame in crossflow. A loudspeaker was used to induce jet pulsations with excitation Strouhal numbers ranging from 0.47 to 1.54 at a pulsation intensity of 0.90. Time-averaged and instantaneous flame images were captured using digital cameras. A customized R-type thermocouple and a commercial gas analyzer were employed to analyze the thermochemical structures. A critical excitation Strouhal number of approximately 0.9, distinguishing two characteristic flame modes: strongly affected flame (SA flame) and weakly affected flame (WA flame), was found. At excitation Strouhal numbers lower than the critical value, the SA flame featured single-peak temperature profiles and low unburned hydrocarbon, carbon monoxide, and nitric oxide emissions. The combustion performance was significantly improved due to the strong mixing effect induced by the acoustic excitation. The WA flame appeared at excitation Strouhal numbers higher than the critical value. It exhibited dual-peak temperature distributions and slightly improved combustion performance. The dynamic behavior and emissions of acoustically excited jet flames offered a fascinating insight into the influence of excitation Strouhal numbers on combustion characteristics. More excitation conditions were expected for future research.