Fundamental Reaction Research Articles

FEATURES OF USING ORTHOPEDIC IMPLANTS ON AN EXPERIMENTAL MODEL OF SENSITIZATION TO NICKEL (NI)

Introduction. The theme of metal hypersensitivity (MHS) reactions is among the most controversial and complex issues in orthopedic and trauma practice. MHS diagnoses are diagnostically challenging because they are exclusionary diagnoses. It is currently uncertain which biomarkers can reliably predict a potential pathological response to implants.
 The aim of this research is to investigate hypersensitivity reactions to orthopedic implants containing nickel (Ni).
 Materials and methods. This research was conducted on female Wistar rats in accordance with the standards of bioethical principles. To obtain conclusive results, the animals were divided into two experimental groups: with prior sensitization to Freund's adjuvant containing Ni and without it. Nickel plates with a total surface area of 24 mm2 were implanted in the rats under general anesthesia. Five months after the intervention, the animals were removed from the experiment, and histological examination of the obtained samples was conducted. Extracted implants were examined using electron microscopy to assess the implant surface. The local elemental composition of the implants was analyzed using an energy-dispersive spectrometer.
 Results. Under the experimental conditions, it was demonstrated that after 5 months following the operation, a dense connective tissue capsule with an inflammatory infiltrate in the capsule lumen had formed around the implants in the rats. This suggests a possible manifestation of hypersensitivity reactions to implants containing Ni. Electron microscopy of the surface of the extracted implants revealed corrosion phenomena in all the samples. The degree of corrosion was more pronounced in the group of animals with prior sensitization to Ni, and distant particles of Ni were detected, which can be characterized as the beginning of implant degradation.
 Conclusions. A connective tissue capsule forms around the implants, and it was found to be 34.8% denser in animals sensitized to Ni prior to implantation, which may indicate tissue reactions with signs of hypersensitivity. Further research will provide a deeper understanding of the fundamental inflammatory and immunological reactions to metals present in implants. This, in turn, will facilitate the identification of clinically useful applications necessary for the development of diagnostic or prognostic tests for patients with metal implants.

Enhancing Oxygen Evolution Reaction Performance: Electrochemical Activation of the Biphasic CoNi/Zn(Fe,Al,Cr)2O4 via Controlled Aluminum Leaching Facilitated Surface Reconstruction

AbstractGiven that the oxygen evolution reaction (OER) faces challenges due to its sluggish kinetics, development of efficient and robust OER catalytic electrodes is critical for reducing the cost of hydrogen production through electrochemical water splitting. In this study, a biphasic CoNi/Zn(Fe,Al,Cr)2O4 coating, characterized by a densely organized stalagmite‐like microarray structure, is deposited on a commercial pure titanium plate, creating an exceptionally effective OER catalytic electrode. The formation of numerous metal/spinel oxide heterogeneous interfaces is demonstrated to enhance its electron transfer ability and conductivity. At high potentials, aluminum leaching and lattice oxygen consumption can facilitate deep surface reconstruction of highly active Fe‐doped CoNiOOH phase inducing electrochemical activation, further optimizing thermodynamic barrier of the fundamental reaction step. Ultimately, this electrode showcases exceptional OER catalytic performance (low overpotential of 248 and 335 mV to deliver the current density of 10 and 100 mA cm−2) compared to commercial IrO2 catalyst (overpotential of ≈310 mV at 10 mA cm−2). Moreover, it demonstrates high current stability sustaining a current density of 500 mA cm−2 for 100 h. This work deepens the comprehension of the surface reconstruction process in OER and, more broadly, introduces a new avenue for designing and enhancing the performance of catalytic materials.

Mechanism of Borane‐Catalyzed Oligomerization of Arylallenes and Arylacetylenes

AbstractRecently, it was shown that Piers’ borane [HB(C6F5)2]2 can induce rapid oligomerization reactions of arylacetylenes and arylallenes. Using phenylallene PhCH=C=CH2 and phenylacetylene PhCCH as typical substrates, the detailed mechanisms of borane‐induced oligomerization are disclosed by extensive state‐of‐the‐art DFT calculations. Following initial regioselective hydroboration of unsaturated C=C or C≡C bonds, further oligomerization and structural rearrangement reactions may occur through unique boryl‐enabled conversions such as 1,3‐boryl‐shift, allylboration, 1,2‐carboboration, and 1,5‐electrocyclization. Together with stepwise transborylation with hydroboranes such as pinacolborane HBpin, such fundamental reactions may pave a catalytic way to borane‐induced oligomerization of arylacetylenes and arylallenes.

Selective Reduction of Nitro Compounds by Organosilanes Catalyzed by a Zirconium Metal-Organic Framework Supported Salicylaldimine-Cobalt(II) Complex.

Reducing nitro compounds to amines is a fundamental reaction in producing valuable chemicals in industry. Herein, the synthesis and characterization of a zirconium metal-organic framework-supported salicylaldimine-cobalt(II) chloride (salim-UiO-CoCl) and its application in catalytic reduction of nitro compounds are reported. Salim-UiO-Co displayed excellent catalytic activity in chemoselective reduction of aromatic and aliphatic nitro compounds to the corresponding amines in the presence of phenylsilane as a reducing agent under mild reaction conditions. Salim-UiO-Co catalyzed nitro reduction had a broad substrate scope with excellent tolerance to diverse functional groups, including easily reducible ones such as aldehyde, keto, nitrile, and alkene. Salim-UiO-Co MOF catalyst could be recycled and reused at least 14 times without noticeable losing activity and selectivity. Density functional theory (DFT) studies along with spectroscopic analysis were employed to get into a comprehensive investigation of the reaction mechanism. This work underscores the significance of MOF-supported single-site base-metal catalysts for the sustainable and cost-effective synthesis of chemical feedstocks and fine chemicals.

Determination of Electrode Kinetics Parameters from Dynamic Electrochemical Impedance Spectroscopy Measurements via Potential-Program Invariant Functions.

Dynamic electrochemical impedance spectroscopy, dEIS, comprises repetitive impedance spectrum measurements while slow scan-rate voltammetry is running. Its main virtue is the short measurement time, reducing the danger of contamination of the electrode surface. To further the use of dEIS, we have recently elaborated a set of theories aimed at the related data processing for three groups of fundamental electrode reactions: diffusion-affected charge transfer, charge transfer of surface-bound species, and adsorption-desorption. These theories yielded equations by which the voltammograms can be transformed to potential-program invariant forms, allowing an easy calculation of the rate coefficients; similar equations have been derived for the potential dependence of equivalent circuit parameters obtained from the impedance spectra. In this Perspective, the above derivations are condensed into a single, unified one. The theory is recommended to evaluate electrode kinetic measurements, particularly when the potential dependence of rate coefficients is under study.

Incorporation of tin into zirconium phosphate to boost efficient conversion of trioses to lactic acid

Dihydroxyacetone isomerization is a fundamental reaction for the production of lactic acid using different feedstocks. However, achieving excellent catalytic activity and resistance against leaching in water is challenging. Herein, we devised a Sn doped zirconium phosphate as effective heterogeneous catalyst. The incorporation of Sn could remarkably aggrandize the content of strong Lewis acid sites while retain relatively high surface areas. Gratifyingly, this catalyst exhibits enhanced activity and reusability for selective dihydroxyacetone isomerization into lactic acid with water as solvent. High lactic acid yields of 70.30 and 76.25% were achieved in water and water/acetone under optimal reaction conditions, respectively. The composition and activity of catalyst are reserved with reduced ions leaching. The excellent catalytic performance is attributed to accelerated conversion of pyruvaldehyde to lactic acid by the strong Lewis acid sites. Nuclear magnetic resonance revealed that the reaction is proceeded via a keto-enol tautomerization process.

Through the interface: New insights of the hydrogen evolution and oxidation reactions in aqueous solutions

AbstractHydrogen evolution and oxidation reactions (HER/HOR) are the most fundamental reactions in electrocatalysis. Despite the practical significance, the mechanisms of HER/HOR in aqueous solutions are still elusive. Various theories have been proposed to rationalize the pH effect, cation effect, and structure effect of HER/HOR but none of them can explain all observations. In this review, we discuss four schools of thought for the HER/HOR, focusing on the strengths and shortcomings of each hypothesis and highlighting the magnitude of electrochemical interface structure in hydrogen electrocatalysis.

Nanosheet architecture of MnO2/carbon with improved reaction kinetics toward advanced zinc energy storage

Aqueous zinc ion batteries (AZIBs) hold substantial promise for large-scale energy storage system by virtue of their good safety and cost-effectiveness. However, the typical cathode material of MnO2 is practically hampered by poor rate/cycling performance owing to its low electrical conductivity and structural fragility. Herein, a nanosheet architecture of MnO2/carbon is constructed via in situ rooting MnO2 nanoarrays on carbon substrate to achieve high-rate and long-durable zinc energy storage. The unique nano-architecture significantly promotes the reaction kinetics by supplying plentiful active sites, short diffusion pathways, and improved charge transfer conductivity. The advantageous features endow the MnO2/carbon with remarkable rate capability (175 mAh/g at 3.0 A/g) and excellent cycling lifespan (87.8 % capacity retention after 1000 cycles at 1.0 A/g). In addition, the kinetic enhancement and fundamental reaction mechanism are systematically investigated. The encouraging results will shed new insight on designing MnO2-based materials to advance the development of AZIBs.

Niobium Oxide Nanorods Obtained by Hydrothermal Synthesis—Structure, Morphology, and Electrochemical Detection of Oxygen Via Oxygen Reduction Reaction

Niobium oxides are promising materials for applications within various research fields, especially as electrocatalysts for various chemical reactions. The tuning of the synthetic parameters can achieve a successful compromise between morphology and structure, aiming to obtain certain properties. Hence, this study aimed to investigate the influence of hydrothermal synthesis parameters on the morphology and structure of niobium oxide growth on a niobium metallic plate. The effect of annealing on the material performance was also evaluated. Afterward, the most crystalline sample was tested for the electrochemical determination of dissolved oxygen, a fundamental reaction in corrosion, biomedicine, and environmental monitoring. This is the first work using this material configuration as an electrochemical sensor. The hydrothermal synthesis produced nanorods formed by poorly crystalline, acidic, hydrated Nb2O5. Increasing the mineralizer concentration could increase the crystallinity and the nanorod growth rate, but it could also promote a lack of structural and morphological uniformity throughout the surface. Heat treatment allowed the increase in crystallinity and favored orthorhombic Nb2O5. Raman spectroscopy revealed that, at the first moment, acidic, hydrated niobium oxide structures were formed as precursors of crystalline niobium oxide that would be developed with longer reaction times and a higher mineralizer concentration. The obtained niobium oxide showed electrocatalytic activity toward the oxygen reduction reaction, with comparable performance between the samples with and without heat treatment. At all analyzed pH values, the amperometric response was linearly correlated with the dissolved oxygen concentration. pH influenced the sensitivity of the material; a maximum sensitivity of 0.0417 mA/cm2·mg/L O2 was achieved at pH = 6. The participation of the acidic functionalities of the surface in the ORR reaction was confirmed by Raman spectroscopy.

Energy-efficient anodic reactions for sustainable hydrogen production via water electrolysis

Overall water splitting is considered as an effective technique for hydrogen (H2) production; however, it usually requires large operating voltage mainly due to the high equilibrium potential of the anodic oxygen evolution reaction (OER). Replacing OER with energy-saving anode reactions not only reduces the operating voltage for H2 production but also generates high-value-added chemicals or purifies wastewater. This review article provides an overview of the fundamental reaction principles of overall water splitting and typical energy-saving alternative anode reactions, including methanol oxidation, hydrazine oxidation, and urea oxidation reactions. Then, the preparation methods, regulation strategies, and composition/structure-performance relations of advanced catalysts for these energy-efficient H2 generation technologies are discussed. Finally, we propose the underlying challenges and perspectives for this promising field.

Thermal Safety of 1-Ethyl-3-Methylimidazolium Bis(trifluoromethylsulfonyl)imide for Construction-Related Safety Process

The surge in demand for sustainable materials has instigated significant research into versatile substances applicable in fields ranging from everyday commodities to construction and energy. Among these, ionic liquids, notably 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIM][Tf2N]), have risen to prominence as green solvents. However, an urgent demand exists to comprehend their thermal safety characteristics, particularly for energy applications. Contrary to previous research, which predominantly employed linear fitting or empirical formulas, our study presents a novel non-linear fitting approach to investigate the thermal behavior of [EMIM][Tf2N]. It yields new insights into its activation energy value, marking a significant advance in attaining precise thermal safety data for sustainable construction applications. To ensure safety at elevated temperatures, [EMIM][Tf2N] was selected for comprehensive analysis. Our research evaluated the kinetic model using thermogravimetric analysis coupled with assessing fundamental reaction parameters and simulating thermodynamic equations by identifying hazardous temperatures. This study revealed that the reactivity hazard of [EMIM][Tf2N] escalated considerably when the temperature surpassed 280 °C, emphasizing the importance of process safety. Furthermore, when the temperature exceeded 287 °C, the time to reach the maximum reaction rate (TMR) diminished to less than a day—an aspect crucial to process safety. At temperatures beyond 300 °C, around 70% of the substance was consumed, further underlining the need for stringent safety measures in processing environments. We also considered the impact of different storage containers on thermal safety. The potential runaway temperatures for box-shaped and cylindrical storage containers were established at 270 °C and 280 °C, respectively, providing valuable data for designing safe storage environments. Our research significantly contributes to the prudent utilization and sustainable application of ionic liquids like [EMIM][Tf2N] by considering various safety scenarios and establishing safe temperature ranges.

Experimental and Modeling Study on the Ignition Kinetics of Nitromethane behind Reflected Shock Waves.

Nitromethane (NM) is the simplest nitroalkane fuel and has demonstrated potential usage as propellant and fuel additive. Thus, understanding the combustion characteristics and chemistry of NM is critical to the development of hierarchical detailed kinetic models of nitro-containing energetic materials. Herein, to further investigate the ignition kinetics of NM and supplement the experimental database for kinetic mechanism development, an experimental and kinetic modeling analysis of the ignition delay times (IDTs) of NM behind reflected shock waves at high fuel concentrations is reported against previous studies. Specifically, the IDTs of NM are measured via a high-pressure shock tube within the temperature from 900 to 1150 K at pressures of 5 and 10 bar and equivalence ratios of 0.5, 1.0, and 2.0. Brute-force sensitivity analysis and chemical explosive mode analysis in combination with reaction path analysis are employed to reveal the fundamental ignition kinetics of NM. Finally, a skeletal mechanism for NM is derived via the combination of directed relation graph-based methods, which demonstrates good prediction accuracy of NM ignition and flame speeds. The present work should be valuable for understanding the combustion chemistry of NM and the development of the fundamental reaction mechanism of nitroalkane fuels.

Reaction kinetics of basaltic elements in cementitious matrices: theoretical considerations

Basalt fibers, the frequently mentioned alternative to those made of steel, possess very good mechanical properties and temperature resistance. The alkaline environment of cement matrix makes it vulnerable due to partial fiber decomposition by the effects of OH- ions. This paper aims at computational modelling of such reactions in order to approximate the course of degradation or to predict it lately. The isothermal reaction models are discussed to reveal their strong/weak points by means of fundamental reaction mechanisms analysis. The shape factor and diffusion-based deceleration of the reactions are mentioned as the most significant ones in that respect. The model accuracy is quantified based on fitting the modelling outputs to reference experimental data. The effect of discussion was found to be the most significant factor as the model fitting reached the lowest RMSE (0.0047). Further application of a diffusion model is therefore recommended. The geometrical models need to have reaction rate reduction explicitly incorporated in the reaction constant, otherwise inapplicable data is produced (RMSE = 0.0193).

A Paradigm Shift in Catalysis: Electro- and Photomediated Nickel-Catalyzed Cross-Coupling Reactions.

ConspectusTransition-metal catalyzed cross-coupling reactions are fundamental reactions in organic chemistry, facilitating strategic bond formations for accessing natural products, organic materials, agrochemicals, and pharmaceuticals. Redox chemistry enables access to elusive cross-coupling mechanisms through single-electron processes as an alternative to classical two-electron strategies predominated by palladium catalysis. The seminal reports of Baran, MacMillan, Doyle, Molander, Weix, Lin, Fu, Reisman, and others in merging redox perturbation (photochemical, electrochemical, and purely chemical) with catalysis are pivotal to the current resurgence and mechanistic understanding of first-row transition metal-based catalysis. The hallmark of this redox platform is the systematic modulation of transition-metal oxidation states by a photoredox catalyst or at a heterogeneous electrode surface. Electrocatalysis and photocatalysis enhance transition metal catalysis' capacity for bond formation through electron- or energy-transfer processes that promote otherwise challenging elementary steps or elusive mechanisms. Cross-coupling conditions promoted by electrocatalysis and photocatalysis are mild, and bond formation proceeds with exceptionally high chemoselectivity and wide functional group tolerance. The interfacing of abundant first-row transition-metal catalysis with electrocatalysis and photocatalysis has brought about a paradigm shift in cross-coupling technology as practitioners are quickly applying these tools in synthesizing fine chemicals and pharmaceutically relevant motifs. In particular, the merger of Ni catalysis with electro- and photochemistry ushered in a new era for carbon-carbon and carbon-heteroatom cross-couplings with expanded generality compared to their thermally driven counterparts. Over the past decade, we have developed enabling photo- and electrochemical methods throughout our combined research experience in industry (BMS, AstraZeneca) and academia (Professor Baran, Scripps Research) in cross-disciplinary collaborative environments. In this Account, we will outline recent progress from our past and present laboratories in photo- and electrochemically mediated Ni-catalyzed cross-couplings. By highlighting these cross-coupling methodologies, we will also compare mechanistic features of both electro- and photochemical strategies for forging C(sp2)-C(sp3), C(sp3)-C(sp3), C-O, C-N, and C-S bonds. Through these side-by-side comparisons, we hope to demystify the subtle differences between the two complementary tools to enact redox control over transition metal catalysis. Finally, building off the collective experience of ourselves and the rest of the community, we propose a tactical user guide to photo- and electrochemically driven cross-coupling reactions to aid the practitioner in rapidly applying such tools in their synthetic designs.

Micellar Solubilization for High‐Energy‐Density Aqueous Organic Redox Flow Batteries

AbstractHigh solubility of active materials is crucial for achieving a high‐energy‐density catholyte/anolyte in redox flow batteries. However, solubility largely depends on the compatibility with electrolyte, limiting the types of redox‐active materials that can be used in aqueous electrolytes. Herein, a universal strategy is introduced to attain a high solubility of active materials regardless of the compatibility with aqueous electrolytes while preserving their intrinsic redox activity via micellar solubilization. Leveraging the amphiphilic nature of surfactant molecules, insoluble redox‐active materials are encapsulated by surfactants to be dissolvable with significant solubility. As a demonstration, it is showed that an order‐of‐magnitude solubility enhancement can be achieved for (2,2,6,6‐tetramethylpiperidin‐1‐yl)oxyl (TEMPO) in aqueous catholyte (≈0.8 m). Consequently, the catholyte performance of TEMPO is fully harnessed, leading to an energy density enhancement of more than ten times compared to that in bare electrolyte. It is also observed that micellar solubilization unexpectedly improves the cycle stability, attributed to the mitigation of intermolecular side reactions and reduced crossover. Finally, the fundamental electrochemical reaction mechanism of micelle‐encapsulated TEMPO is discussed. This strategy offers a new insight regarding the solubility and stability of the catholyte/anolyte, and is expected to be applicable to other redox‐active molecules, opening up an unexplored micellar chemistry in redox flow batteries.

Biomimetic asymmetric transamination reactions catalyzed by axial pyroxamine organocatalysts: Mechanism and origin of stereoselectivity

Biomimetic asymmetric transamination reactions have emerged as a focal point within the organocatalysis domain, generating substantial interest. However, the detailed mechanism and origin of stereoselectivity are remains elusive. Within this context, we present an exhaustive theoretical investigation into the detailed mechanism and origin of stereoselectivity governing such reactions between α-keto acids and amines catalyzed by axial pyroxamine. The fundamental reaction pathway can be divided into two stages, i.e. amino transfer stage to form chiral amine product and imine hydration stage for the generation of ketone product. To uncover the mystery of the chiral center produced by protonation in the amino transfer stage, five possible pathways were investigated and compared. This thorough examination unequivocally identifies the HOAc-assisted [1,3]-proton transfer as the pivotal step dictating stereoselectivity within the most energetically advantageous route. Further atoms-in-molecules (AIM) analysis was carried out to predict the origin of stereoselectivity. Notably, the N–H⋯O hydrogen bond interaction occurring between the pyridoxamine catalyst and α-keto acid of substrate has been pinointed as the driving force responsible for the energetical favorability of S-configurational pathway. These insights will be of great value for understanding and rational design of biomimetic organocatalysts for transamination reactions.

(Invited) Photoinduced Electron Transfer in Dyads Involving Complexes of C60 and Nanohoops. Effect of π-Extension and Aromaticity of the Nanohoop

Conversion of the sunlight into chemical energy is considered to be one of the most important and fundamental chemical reactions in nature. A broad variety of artificial photosynthetic systems based on dyads, triads and up to pentads involving electron donor and acceptor moieties have been designed and synthesized in order to investigate artificial photoinduced energy and electron transfer processes. One type of dyads with potential applications in solar cells is the one combining C60 complexed with nanohoops.[1] In this work, we discuss a series of computational studies that involves the photoinduced charge separation in complexes of C60 and Li+@C60 with a series of different nanohoops, such as the [10]cycloparaphenylene ([10]CPP) ring,[2] π-extended CPPs such as the hexa-peri-benzocoronene (HBC) or the tribenzo[fj,ij,rst]pentaphene (TBP),[3] and [n]cyclodibenzopentalenes ([n]CDBPs) as antiaromatic curved nanorings.[4] The analysis of complexes of C60 with nanohoops having different degrees of π-conjugation and aromaticity allow us to discuss the effect in the charge transfer separation and recombination on the level of π-extension and aromaticity present in the nanohoops.

Experimental Determination of the Intrinsic Oxygen Reduction Kinetics on Polycrystalline Platinum and the Role of the Adsorbed Oxygen

The Oxygen Reduction Reaction (ORR) is a fundamental reaction in electrochemical devices such as fuel cells and sensors. The ORR only occurs on few catalytically active surfaces, mainly platinum and its alloys and understanding its mechanism is critically important to develop new catalysts and applications. In contrast to the related Hydrogen evolution/oxidation reaction, the intrinsic ORR activity is rarely determined due to simultaneous formation of Pt-O species. Therefore, the ORR activity is measured at a benchmark potential making its susceptible to the measurement characteristics, such as "activation", scan rate, and scan direction.We found that by using a specially designed experimental procedure one can separate the effect of Pt-O on the ORR kinetics without extensive modelling or fitting. As a results an exemplary Pt-O corrected Tafel plot on polycrystalline platinum is displayed in figure 1.In this presentation we will discuss the underlying method, its application on a range of different ORR environments, the nature of the Pt-O species, and the implications for ORR mechanism itself. Figure 1

Oxidative Addition of Aryl Electrophiles into a Red-Light-Active Bismuthinidene.

The oxidative addition of aryl electrophiles is a fundamental organometallic reaction widely applied in the field of transition metal chemistry and catalysis. However, the analogous version based on main group elements still remains largely underexplored. Here, we report the ability of a well-defined organobismuth(I) complex to undergo formal oxidative addition with a wide range of aryl electrophiles. The process is facilitated by the reactivity of both the ground and excited states of N,C,N-bismuthinidenes upon absorption of low-energy red light.

Insights into the pyrolysis mechanisms of epoxy resin polymers based on the combination of experiments and ReaxFF-MD simulation

Epoxy resin offers promising properties in composites, while its cross-linked structure prevents the disposal of waste composites. Pyrolysis is an essential technique for the breakdown of epoxy resin polymers, but the fundamental reaction mechanisms need to be clarified. In this study, the combination of experimental studies and the reactive force field molecular dynamic (ReaxFF-MD) simulation were performed to determine the formation mechanisms of pyrolysis products considering the secondary reactions of intermediates. The pyrolysis process was divided into the cleavage and polycondensation stages based on the carbon atom numbers of the largest cluster. The cleavage stage began with the removal of side-chain substituents, followed by the breakdown of the primary epoxy resin chain, resulting in the generation of pyrolysis gas products, of which the OH, C-C-O, and CH3 groups were identified as the critical intermediates in the creation of H2O, CO, and CH4, respectively. Meanwhile, the simultaneous evolution of liquid pyrolysis products (bisphenol A, phenol, and benzene) was established. After the epoxy resin chains were completely cracked, the unsaturated hydrocarbon intermediates underwent the dehydrogenation and polymerization reactions, causing the formation of pyrolysis char and the continuous generation of H2, H2O, and CO. The findings could provide some guidance to selectively regulate the pyrolysis of epoxy resin matrix composites.