Time Of Reaction Research Articles

Fully Integrated Microfluidic Device for Magnetic Bead Manipulation to Assist Rapid Reaction and Cleaning.

Methods to manipulate magnetic beads are essential factors to determine the efficiency and dimension of an in vitro diagnostic system. Currently, using movable permanent magnets and planar electromagnets is still the major approach to achieve magnetic bead control, causing significant constraint in the miniaturization of in vitro diagnostic systems. Here, we propose techniques to construct a fully integrated microfluidic device that can conduct automatic magnetic bead manipulation as well as rapid chemical reaction and cleaning in a minimized dimension similar to a USB disk. The device combines the precision control of multiple electromagnetic coils with the compactness of microfluidic channels, leading to one of the smallest automatic magnetic bead manipulation systems that can complete several major magnetic bead-based operation steps such as sample injection, reaction, cleaning, and collection. The influencing factors such as coil driving parameters, surface treatment of the microchannels, and properties of magnetic particles have also been investigated to optimize the device performance. The device can drive mixtures of Fe3O4 microparticles and polymer magnetic beads (PMBs) with a weight ratio of 1:1 at a maximum speed of 0.5 cm·s-1 and reduce the time for DNA binding and dissociation reactions from 20 min to only 48 s. This device has significantly advanced the conventional manipulation methods of magnetic beads and has demonstrated the possibility to construct an automatic and ultraminiaturized in vitro diagnostic system that may facilitate portable or even wearable chemical analysis.

A novel SPE-UPLC-MS/MS-based assay for the selective, simultaneous quantification of xylosyltransferase-I and -II activity

Xylosyltransferase-I and -II (XT-I, -II) possess a central role during the glycosylation of proteoglycans (PGs). They catalyze the formation of an O-glycosidic bond between the xylosyl residue of uridinediphosphate-xylose and the core protein of a PG. Thereafter, three following glycosyltransferases lead to the generation of a tetrasaccharide linker, which connects the PG core protein to the respective glycosaminoglycan.The selective quantification of XT-I and XT-II activity is of biological and clinical interest due to their association with fibrotic processes and skeletal dysplasia. There is no assay available to date that simultaneously determines the activity of the two XT isoforms. Although an XT-I selective UPLC MS/MS-based assay was published by Fischer et al., in 2021, the determination of XT-II activity can only be performed simultaneously by the improved assay presented here. To establish the assay, two synthetic peptides, selectively xylosylated by the respective isoform, were identified and the associated measurement parameters for the mass spectrometer were optimized. In addition, the quantitative range of the xylosylated peptides were validated, and the incubation time of the enzyme reaction was optimized for cell culture samples and human sera. The specific enzyme kinetics (KM and Vmax) of the respective XT isoform for the two peptides were also determined. Subsequently, a mathematical model was developed, allowing the simultaneous determination of XT-I and XT-II activity from the chromatographic results.Summarized, a mass spectrometric method suitable for the simultaneous analysis of XT-I and XT-II activity in cell culture lysates, supernatants and human sera was successfully developed.

Photocatalytic Decolorization of Crystal Violate Dye Solution by ZnO/MWCNT Nanocomposite

By extracting crystal violate dye (CV) from its aqueous solution, the photocatalytic decolorization performance of ZnO/MWCNT nanocomposite was evaluated. The nanocomposite was prepared by precipitation of ZnO and incorporates on the surface of Multi-Walled Carbon Nanotubes (MWCNT). ZnO nanoparticles were synthesized using the sol gel process with MWCNT acting as a template. They were then analyzed by XRD, SEM, and TEM, which revealed how the shape of the spherical nano ZnO interacts with the point of zero charge (pzc), which allows us to see the physical attributes. In the dipping photoreactor, which included a slurry of dye solution and ZnO/MWCNT nanocomposite, the effectiveness of decolorization was assessed. The photodecolorization was studied for CV dye in aqueous solution at different conditions: The effect of time, weight of catalyst, concentration of dye, temperature, the initial pH of dye solution and addition of S2O82- to show the optimum condition of this process. The main results were the synthesis of incorporated ZnO on MWCNT surface with 10-20 nm with high photodecolorization against CV dye. Full decolorization reached at 90 min and 89.8% decolorization at the half time of reaction. ZnO/MWCNT weight of 0.06 gm per 100 mL was optimum for photodecolorization. The photocatalytic reaction was more efficient in the deceasing of CV concentration and obeys the Langmuir-Hinshelwood kinetic, while the photodecolorization was not less than 95% in pH range 6-10.Also, the photocatalytic reaction was effected in the presence of S2O82-, where the photodecolorization was more efficient.

Event-triggered impulsive control for synchronization in finite time of fractional-order reaction–diffusion complex networks

This paper is concerned with the finite-time synchronization (FTS) issue for fractional-order reaction–diffusion complex networks (RDCNs). A finite-time stability principle, which plays a key role in the synchronization analysis later, is developed for fractional-order nonlinear impulsive system. A novel hybrid controller, which consists of a event-triggered controller and a impulsive controller, is designed to realize the global FTS objective for the considered network. By applying the Lyapunov stability theory and the fractional calculus, the global FTS conditions are addressed in the form of algebraic inequalities. In addition, the exclusion of Zeno behavior are proved for the designed event-triggered strategy. Finally, a numerical example is provided to illustrate the feasibility of the proposed control approach and the correctness of the theoretical results.

Ultra small carbon dots from Crocus cancellatus as a highly fluorescence probe for synthetic Ponceau 4R dye sensing in food samples

In this work, for the first time, natural Crocus cancellatus was adopted for the green, low-cost, and simple synthesis of highly fluorescent ultra-small carbon dots (CDs) with well-distributed size using a one-pot hydrothermal treatment. As-synthesized CDs are used as fluorescence sensing probe for quantitative analysis of Ponceau 4R (E124) synthetic food dye, which is widely used. However, excessive consumption of Ponceau 4R poses potential health risks. To obtain better-quality performance of as-synthesized CDs, the time and temperature of the hydrothermal carbonization reaction of crocus were optimized simply. The as-prepared carbon dots exhibit exceptional advantages including excellent fluorescence, satisfactory chemical stability, low toxicity, and excellent biocompatibility. It produced a strong blue fluorescence when irradiated with UV light at 365 nm, which was subsequently effectively employed for Ponceau 4R sensing based on the quenching of fluorescence. The as-prepared CDs was characterized by EDX, XRD, FTIR, SEM, HRTEM, UV–Visible absorption spectrophotometry, and fluorescence. The effects of carbon dots fluorescence emission wavelength, CDs quantity, pH value, and reaction time were investigated to detect Ponceau 4R under optimum conditions. The synthesized carbon dot's fluorescence intensity allowed quantitative determination of Ponceau 4R in the linear range of 60–6000 nM with a detection limit of 40 nM that is lower than all previously published methods. Several soft drink samples were used to validate the potential use of this new fluorescent probe for P4R detection in actual samples with good precision and accuracy.

Influence of DNP Polarizing Agents on Biochemical Processes: TEMPOL in Transient Ischemic Stroke.

Hyperpolarization of 13C by dissolution dynamic nuclear polarization (dDNP) boosts the sensitivity of magnetic resonance spectroscopy (MRS), making possible the monitoring in vivo and in real time of the biochemical reactions of exogenously infused 13C-labeled metabolic tracers. The preparation of a hyperpolarized substrate requires the use of free radicals as polarizing agents. Although added at very low doses, these radicals are not biologically inert. Here, we demonstrate that the presence of the nitroxyl radical TEMPOL influences significantly the cerebral metabolic readouts of a hyperpolarized [1-13C] lactate bolus injection in a mouse model of ischemic stroke with reperfusion. Thus, the choice of the polarizing agent in the design of dDNP hyperpolarized MRS experiments is of great importance and should be taken into account to prevent or to consider significant effects that could act as confounding factors.

Green Synthesis and Biological Study of New Imidazothiazines Using New MCRs: A Combined Experimental and Theoretical Investigation

For the performing this research multicomponent reaction of isatin, electron-deficient acetylenic compounds, α-haloketones, ammonium acetate, isothiocyanates and methyl aziridine in aqueous at room temperature was investigated for the production of novel derivatives of azepinothiazine in excellent yields. The synthesized azepinothiazines have OH, NH2 and NH functional groups that have acidic hydrogen and show high antioxidant activity. These synthesized compounds also displayed antimicrobial activity by using the disk diffusion procedure and two Gram-positive and Gram-negative bacteria. Also, to better understanding reaction mechanism density functional theory-based quantum chemical methods have been applied. The employed process for the production of azepinothiazine has some benefits such as short time of reactions, excellent efficiency of the product, easy separation of products.

Lipase as Biocatalyst- for Synthesis of Phenol by Using Box–Behnken Design

This work highlighted the proficient and naturally safe methodology for the phenol synthesis using biocatalyst lipase. The development of sustainable synthetic protocol for various organic transformations is an important area of research attracts researchers to avoid use of volatile and hazardous organic solvents in reaction for greener and eco-friendly protocols. Lipase is subclass of esterase enzymes and acts as biocatalyst with industrial significance. They carry out biochemical transformation in non-aqueous and aqueous phases quickly. To further make the process more specific Design Expert software was used for the optimization of synthesize phenol for maximum % Yield and % Purity. Effect of temperature, Concentration of Catalyst, and Volume of Water was selected as an independent factor to get the maximum % Yield and % Purity of the phenol. The results confirmed the mathematical model robustness and justify experimental design. Therefore, the current protocol for synthesis of phenols from phenylboronic acid is greenest and environmentally benign alternative. The current convention has many benefits, like phenomenal product yields, reduced time of reaction, simple procedure to work up, and extensive substrate scope, cost-effective and also lipase was recuperated and reused multiple times without significant loss of its catalytic activity.

Microwave-Processable Cu Nanostructures -the Morphology and Chemical Properties

The work presented a facile method using a domestic microwave-assisted technique in synthesising the Cu nanostructures solution. By controlling the microwave reaction time, the morphological structures and the ultra-fast growth of the as-synthesised Cu nanostructures are varied. The method is much preferable as compared to the conventional hydrothermal method due to the ultrafast supersaturation of Cu nuclei and high-quality structures. Those different morphologies with different average size distributions show a direct influence on their intrinsic physical behaviour. The study focuses on the morphology, particle size distribution and element bonding effect of the growth reaction and solution’s concentration. The combination of the CuSO4·5H2O, PEG (polyethylene glycol) and PVP (polyvinyl pyrrolidone) without any extra reagents shows the capabilities of mixture to yield the Cu nanostructures with the average particle size distribution below 100 nm. The produced Cu nanostructures via microwave-assisted demonstrated that the allocated time of reaction (∼7 mins) shows a good supersaturated homogeneous nucleated suspension yield. Simultaneously, they undergo a size-dependent multi-stage aggregation mechanism to yield different morphologies of Cu nanostructures.

Fixing CO2 under Atmospheric Conditions and Dual Functional Heterogeneous Catalysis Employing Cu MOFs: Polymorphism, Single-Crystal-to-Single-Crystal (SCSC) Transformation and Magnetic Studies.

New copper compounds, [Cu(C14H8O6)(C10H8N2)(H2O)] (1), [Cu(C14H8O6)(C10H8N2)(H2O)]·(C3H7ON)2 (2), [Cu(C14H8O6)(C10H8N2)(H2O)2]·(C3H7ON) (3), [Cu(C14H8O6)(C10H8N4)] (4), and [Cu(C14H8O6)(C10H8N4)]·(H2O) (5), were prepared employing 2,5-bis(prop-2-yn-1-yloxy)terephthalic acid (2,5-BPTA) as the primary ligand and 4,4'-bipyridine (1-3) and 4,4'-azopyridine (4-5) as the secondary ligands. Single-crystal studies indicated that compounds 1-4 have two-dimensional layer structures and compound 5 has a three-dimensional structure. Compounds 1-3 were isolated from the same reaction mixture but by varying the time of reaction. The framework structures of compounds 1-3 are similar and may be considered as polymorphic structures. Compounds 4 and 5 can also be considered polymorphic with a change in dimensionality of the structure. Compounds 1-3 can be formed through a single-crystal-to-single-crystal transformation under a suitable solvent mixture. The Cu center was explored for the Lewis acid-catalyzed cycloaddition reaction of epoxide and CO2 under ambient conditions in a solventless condition and also for the synthesis of propargylamine derivatives by three-component coupling reactions (A3 coupling) in a DCM medium. The Lewis basic functionality of the MOF (-N═N- group) has been explored for the Henry reaction (aldol condensation) in a solventless condition. In all of the catalytic reactions, good yields and recyclability were observed. The magnetic studies indicated that compounds 1 and 4 have antiferromagnetic interactions and compound 5 has ferromagnetic interactions. The present studies illustrated the rich diversity that the copper-containing compounds exhibit in extended framework structures.

Glucose-Histidine Heyns compound: Preparation, characterization and fragrance enhancement

N-(2-Deoxy-D-glucos-2-yl)-L-histidine (Glu-His), one of Heyns rearrangement products (HRPs), was prepared by condensation, dehydration and rearrangement using l-Histidine and d-Fructose as raw materials with methanol as solvent. The response surface method (RSM) was used to improve yield of product and the optimal reaction condition was as following: the original ratio of Fru:His was 1.2:1 and the temperature and time of reaction was 73.2 °C and 4.7 h, and the yield of final product was 74.10% with the purity of 99.7%. The structure of product was identified by IR, NMR and conformed as C12H19N3O7 (317.1 Da) by high-resolution mass spectrometry (HRMS) and UPLC-MS/MS. The pyrolysis behavior of Glu-His showed that its initial pyrolysis temperature was 145.2 °C and the total weight loss reached 70.61% at 800 °C. The number of pyrolysis products increased with the increase of temperature, and the main pyrolysis products were pyrans, furans, pyrazines, pyrroles, pyridines, indoles and etc. with burnt-sweet, baking, nutty, sweet and floral aroma features. At last, the fragrance enhancement effect of Glu-His in the preparation of reconstructed tobacco stem (RTS) was investigated and the result of sensory evaluation showed that the smoke of RTS cigarettes brought about more sweet and moist, less irritation, better flavor and comfort with the addition of Glu-His (0.25%, w/w).

Transient Receptor Potential channels (TRP) in GtoPdb v.2023.2

Transient Receptor Potential channels (TRP) in GtoPdb v.2023.2

Synthesis, Theoretical Study and Investigation of Biological Activity of Imidazolidine Derivatives

In this work we synthesized imidazolidine derivatives in excellent yields using multicomponent reactions of phthalaldehyde or its derivatives, primary amines, isothiocyanate, 2,4-dihydroxyacetophenone and isopropenylacetylene in the presence of catalytic amount of Ag/KF/CP@MWCNTs NCs in water at room temperature. Also, the catalytic activity of the green synthesized Ag/KF/CP@MWCNTs NCs was evaluated in the reduction of organic pollutants such as 4-nitrophenol (4-NP) in water at mild conditions. The results indicated that the biosynthesized NCs have very high and effective catalytic activity for organic pollutants within few seconds. As well the antioxidant activity of some synthesized imidazolidine was studied using trapping of radical by DPPH and ferric reduction activity potential (FRAP) experiment. Also, the antimicrobial activity of some synthesized compounds proved by employing the disk diffusion test on Gram-positive and Gram-negative bacteria. Also, to better understanding reaction mechanism density functional theory (DFT) based quantum chemical methods have been applied. The short time of reaction, high yields of product, easy separation of catalyst and products are some benefits of this procedure.

Microwave-assisted Synthesis of Pharmacologically Active 4-Phenoxyquinolines and their Benzazole-quinoline Hybrids Through SNAr Reaction of 4,7-dichloroquinoline and Phenols Using [bmim][PF6] as a Green Solvent.

Quinoline and its derivatives have been shown to display a wide spectrum of biological properties, especially anticancer activity. Particularly, diverse potent anticancer drugs are based on the 4-phenoxyquinoline skeleton, acting as small-molecules VEGR2 and/or c-Met kinase inhibitors. However, the design of new drugs based on these quinoline derivatives remains a challenge. Up till now, all approaches to 4-phenoxyquinoline skeleton construction do not obey any green chemistry principles. Developing a new, and efficient protocol for the synthesis of potentially bioactive 4-phenoxyquinoline derivatives and benzazole-quinoline-quinoline hybrids from commercially available 4,7-dichloroquinoline and phenol derivatives using microwave energy (MW) in the presence of 1-methyl 3-butylimidazolium hexafluorophosphate. Neweco-efficient protocol for valuable 7-chloro-4-phenoxyquinolines and their hybrids, which is based on SNAr reaction of 4,7-dichloroquinoline with respective simple phenols and hydroxyaryl- benzazoles under MWenergy in green reaction media, is studied for the first time. We found that among various solvents tested, the ionic liquid 1-methyl 3-butylimidazolium hexafluorophosphate ([bmim][PF6]) favored the SNAr reaction affording phenoxyquinolines in excellent yields (72-82%) in 10 min. The developed protocol allowed to obtain quickly in good yields (48-60%) new diverse benzazole-quinoline hybrids, which are expected to be pharmacologically active. According to the calculated bioactivity scores, new hybrids are potential kinase inhibitors that could be useful in anticancer drug research. We developed for the first time a new green, efficient method to prepare potentially bioactive functionalized 7-chloro-4-phenoxyquinolines and benzazole-quinoline molecules. Good to excellent yields of the quinoline products, use of MW irradiation in ([bmim] [PF6] as a green solvent, and short times of reactions are some of the main advantages of this new protocol.

Transfer hydrogenation of furfural to furfuryl alcohol under microwave irradiation using mixed oxides.

The reaction to obtain furan alcohols is one of the most important in the upgrading of furan derivates. An attractive route is the transfer hydrogenation of furfural using acidic-basic catalysts. In this work, mixed oxides derived from ternary hydrotalcites were employed to obtain furfuryl alcohol from furfural assisted by microwave irradiation. The reaction was studied using containing Co2+ and Ni2+ in their structure and was then optimized using distinct primary and secondary alcohols as hydrogen donor sources, as well as distinct temperatures and initial concentrations of furfural. The yields to furfuryl alcohol are strongly dependent on the type of Me2+ in layered oxides mainly due to higher basicity and also to the donor employed in the reaction. The mixed oxide containing Co2+ showed complete conversion of furfural and higher yields to furfuryl alcohol (> 95%) at short times of reaction (< 1 h).

Optimization of iron-ZIF-8 catalysts for degradation of tartrazine in water by Fenton-like reaction

Optimization of iron zeolitic imidazole framework-8 (FeZIF-8) nanoparticles, as heterogeneous catalysts, were synthesized and evaluated by the Fenton-like reaction for to degrade tartrazine (Tar) in aqueous environment. To achieve this, ZIF-8 nanoparticles were modified with different iron species (Fe2+ or Fe3O4), and subsequently assessed through the Fenton-like oxidation. The effect of different parameters such as the concentration of hydrogen peroxide, the mass of catalyst and the contact time of reaction on the degradation of Tar by Fenton-like oxidation was studied by using the Box-Behnken design (BBD). The BBD model indicated that the optimum catalytic conditions for Fenton-like reaction with an initial pollutant concentration of 30 ppm at pH 3.0 were T = 40 °C and 12 mM of H2O2, 2 g/L of catalyst and 4 h of reaction. The maximum Tar conversion value achieved with the best catalyst, Fe1ZIF-8, was 66.5% with high mineralization (in terms of decrease of total organic carbon – TOC), 44.2%. To assess phytotoxicity, the germination success of corn kernels was used as an indicator in the laboratory. The results show that the catalytic oxidation by Fenton-like reaction using heterogeneous iron ZIF-8 catalysts is a viable alternative for treating contaminated effluents with organic pollutants and highlighted the importance of the validation of the optimized experimental conditions by mathematical models.

Facile synthesis of Cu-doped BiVO4 using domestic microwave-assisted chemical precipitation method with fleeting time of microwave irradiation for the photocatalytic application

Semiconductor-based visible light active photo-catalyst has been synthesized through microwave-assisted chemical precipitation method under acidic pH with minimal time of reaction using microwave irradiation. The monoclinic crystal phase of the material with no impurity is confirmed with XRD data. We can observe slight left shift after doping with copper (Cu) in 2Θ peak of XRD data. SEM analysis exhibits a gradual change in morphology with the increase in doping concentration. UV–Vis data confirms an improvement in absorption with the increase in dopant concentration. PL analysis further clarifies the change in recombination rate of photo-induced charge carriers. Photocatalysis has been tested with methylene blue (MB) synthetic dye. The maximum percentage of degradation was determined to be 61.08% and it is obtained for 0.25% Cu-doped BiVO4. It is also observed that 0.25% Cu-doped BiVO4 has lower energy band gap value, i.e., 2.03 eV and lesser PL intensity than pure un-doped BiVO4. The HRTEM analysis proves that 0.25% Cu-BiVO4 is well crystalline in nature with the d spacing corresponding to (121) plane of BiVO4.

Traditional Vietnamese Medicine Containing Garlic Extract for Patients With Non-severe COVID-19: A Phase-II, Double-Blind, Randomized Controlled Trial.

Background Coronavirus disease 2019 (COVID-19) is still ongoing with the omicron variant. Low-cost, effective treatments are still needed, particularly in low-to-middle-income countries. This study assessed the safety and efficacy of TD0068, an herbal medicine developed from mainly garlic, for patients with non-severe COVID-19. Methods This is a phase-II, double-blind, randomized controlled trial to compare oral capsule TD0068 and placebo in adults aged 18-65 years with non-severe COVID-19 between September and October 2021. The efficacy outcomes measured included daily cycle threshold (Ct) value from the time of the initial reverse transcription-polymerase chain reaction (RT-PCR) test, time to viral clearance, daily symptom severity score from 15 symptoms of interest, time to symptom resolution, and progression to severe/critical COVID-19. Safety outcomes included adverse events (AEs) and serious adverse events (SAEs). Results Sixty patients were randomized (31 received TD0068, and 29 received a placebo). The two groups were balanced in baseline characteristics: mean age was 39 years, and female was predominant (66%). Daily Ct value (median on days 3, 5, 7, and 9 was 25.7, 30.8, 35.4, and 37.6 in the TD0068 group, and 26.4, 31.2, 36.0, and 37.4 in the placebo group, respectively) and time to viral clearance (median: 10 vs. 11 days in TD0068 and placebo groups) were similar between groups. Daily symptom severity score (median on days 3, 5, 7, and 9 was 2, 2, 1, and 0 in the TD0068 group, and 3, 2, 1, and 1 in the placebo group), and time to symptom resolution (median: seven vs. nine days, respectively) were also comparable between groups. No SAE occurred in the study. Conclusions TD0068 is safe but does not show an effect for non-severe COVID-19 patients. Further research is needed to explore the potential benefits of garlic in other forms or dosages for the treatment of COVID-19.

Direct growth of AC@NiCo2S4 composite on nickel foam as binder-free electrodes for supercapacitors

In this study, folded nanotubes were directly grown on Ni foam by two-step hydrothermal method to form activated carbon (AC) and NiCo2S4 composite material with a unique structure like nano-urchin. In addition, the morphology and structure can be controlled by the time of hydrothermal reaction. The resulting samples were characterized by means of XRD, XPS, EDS and SEM. The electrochemical test results show that compared with the 6 h and 24 h hydrothermal composites, the 12 h hydrothermal composites (AC@NiCo2S4–2) form a complete folded nanotube structure, provide a large number of reactive sites, and show better electrochemical properties. And compared with the capacitance of NiCo2S4 (456.14 C g−1), the AC@NiCo2S4–2 exhibited a high specific capacitance of 653.9 C g−1 at a current density of 1 A g−1. In addition, after combination with AC, AC@NiCo2S4 has better electrochemical performance and cycle stability, the capacitance retention rate at 10 A g−1 is 62.84 % of 1 A g−1, and can still maintain 84.96 % of the initial capacitance after 3000 cycles. Moreover, the fabricated hybrid supercapacitor (HSC) based on AC@NiCo2S4–2 and AC electrodes achieved a high energy density of 29.75 Wh kg−1 at the power density of 700 W kg−1 and still maintain the energy density of 16.86 Wh kg−1 at the high power density of 7000 W kg−1.

Combustion Intensification Mechanism in a Vortex-Tube Reactive Flow

The combustion intensification mechanism was revealed in a stratified vortex-tube combustor. The results show that a triple-flame structure is formed in this combustor and the peak heat release is located exactly at the triple-point position. The peak heat release rates in the five selected representative cases studied in this paper are all over . The stability limit is wide, and the lean stability limit is always lower than 0.2. The decreased mixing length and decreased velocity difference between the fuel and oxidant streams delay the mixing process and then bring about a stratified distribution of species. This is crucial for the generation of a triple-flame structure and the corresponding high species concentration in the vicinity of the reaction zone under lean conditions. The Damköhler numbers on the lines across the triple points were calculated with values above 1.0 in each of the cases, indicating that the species’ transport time is longer than the chemical reaction time. Therefore, the transport flux of species determines the final combustion strength. The synergistic coupling of the flowfield and species field gives rise to a large transport flux of the key species in the vicinity of the reaction zone. The results show that the corresponding fuel transport flux is large, with values all over . This is the principal reason for the high combustion intensity in this combustor. The different transport fluxes of the critical species are responsible for the different chemical reaction strengths on the triple point in each of the different cases.