High Mass Research Articles

Numerical Simulation and Response Surface Analysis of Esterification of Monobutyl Chlorophosphate with n-Butanol in a Microchannel Reactor

Microreactors are essential for microchemical reactions owing to their high mass transfer efficiency, precise control of reaction time, easy amplification, and good safety performance. These characteristics provide several advantages, including shortened reaction times and enhanced chemical reaction conversion rates, rendering microreactors particularly significant in chemical production. In this study, a finite-rate model was developed for the esterification of monobutyl chlorophosphate (MCP) and n-butanol in a microchannel reactor. This study investigates the impact of the microchannel’s length-to-diameter ratio, the mass ratio of n-butanol to MCP at the inlet, and the inlet flow ratio on the entire reaction system through numerical simulations. The findings indicate that increasing the length-to-diameter ratio and reducing the inlet flow rate effectively prolongs the residence time of materials in the microreactor, thereby enhancing the conversion rate of the reactants. Optimal results are achieved with a moderate n-butanol/MCP mass ratio, which facilitates MCP transformation. Moreover, this study employs response surface analysis to investigate the influence of independent factors, such as the microchannel’s length-to-diameter ratio, component ratio, and inlet velocity ratio, on MCP conversion rates. A prediction formula with conversion rate as the dependent variable and microchannel length-to-diameter ratio, component ratio, and inlet velocity ratio as independent variables was established.

Resolving Atmospheric Oxygenated Organic Molecules in Urban Beijing Using Online Ultrahigh-Resolution Chemical Ionization Mass Spectrometry.

Gaseous oxygenated organic molecules (OOMs) are crucial precursors of atmospheric organic aerosols. OOMs in urban atmospheres have complex compositions, posing challenges to understanding their formation, evolution, and influences. In this study, we identify 2403 atmospheric gaseous OOMs in urban Beijing using online nitrate-based chemical ionization Orbitrap mass spectrometry based on one-year atmospheric measurements. We find that OOMs in urban atmospheres can be identified with higher accuracy and wider coverage, compared to previously used online mass spectrometry. With optimized OOM resolving capabilities, previous knowledge of OOMs in urban atmospheres can be expanded. First, clear homologous and oxygen-addition characteristics of the OOMs are revealed. Second, OOMs with lower concentrations or higher masses are identified and characterized with high confidence, e.g., OOMs with masses above 350 Da. In particular, dimers of OOMs (e.g., C20H32O8-15N2), crucial species for organic nucleation, are identified. During four seasons, nitrogen-containing OOMs dominate the total concentration of OOMs, and OOMs are mainly from aromatic and aliphatic oxidation. Additionally, radicals with similar composition as OOMs, intermediates for OOM formation, are identified with clear diurnal variation, e.g., CnH2n-5O6 radicals (n = 8-10) and CmH2m-4NO9 radicals (m = 9-10), peak during the daytime and nighttime, respectively, previously having scarce measurement evidence in urban atmospheres.

Tidal mass loss in the Fornax dwarf spheroidal galaxy through N-body simulations with Gaia DR3-based orbits

Aims. The Fornax dwarf spheroidal galaxy (dSph) represents a challenge for some globular cluster (GC) formation models, because an exceptionally high fraction of its stellar mass is locked in its GC system. In order to shed light on our understanding of GC formation, we aim to constrain the amount of stellar mass that Fornax has lost via tidal interaction with the Milky Way (MW). Methods. Exploiting the flexibility of effective multi-component N-body simulations and relying on state-of-the-art estimates of Fornax’s orbital parameters, we study the evolution of the mass distribution of the Fornax dSph in observationally justified orbits in the gravitational potential of the MW over 12 Gyr. Results. We find that, though the dark-matter mass loss can be substantial, the fraction of stellar mass lost by Fornax to the MW is always negligible, even in the most eccentric orbit considered. Conclusions. We conclude that stellar-mass loss due to tidal stripping is not a plausible explanation for the unexpectedly high stellar mass of the GC system of the Fornax dSph and we discuss quantitatively the implications for GC formation scenarios.

Chemical profiling of organic contaminants in rural surface waters combining target and non-target LC-HRMS/MS analysis

The pollution of natural waters by contaminants of emerging concern (CECs) is one of the pressing problems due to their global distribution and potential negative effects on the environment and human health. In rural areas with lower population density and limited industrial development, less contamination is expected. However, the lack of wastewater treatment plants (WWTPs) or their poor removal efficiency can lead to significant input of pollutants. In this context, 11 streams of rural areas in the Guadalquivir River basin, southeast of Spain, were studied over two years to obtain an overview of the origin and distribution of contaminants. A target method using solid-phase extraction and liquid chromatography coupled to high resolution mass spectrometry (LC-HRMS) was developed for the analysis of 316 compounds in surface waters. A total of 78 target analytes were detected, comprising pesticides, pharmaceuticals, personal care products (PCPs), transformation products (TPs), and industrial chemicals. The flame retardant tributyl phosphate (16–3572 ng L−1) was detected in all samples, followed by caffeine (30–8090 ng L−1) and the analgesic tramadol (3–1493 ng L−1). The target approach was combined with a non-target analysis (NTA) strategy to obtain an overall perspective of the chemical profile of unexpected or unknown compounds in the samples. Up to 79 contaminants were tentatively identified, and 12 of them were finally confirmed with standards. Most of the contaminants determined by NTA were pharmaceuticals and their TPs. The results indicated that most of CECs have an urban origin despite traditional agriculture is the main economic activity in this region. Moreover, the absence of WWTPs in small towns is significant, as contamination levels at these sites were comparable to or higher than those in larger populations with sewage treatments.

Aspects of arterial hypertension in young adults with obesity

The global prevalence of hypertension and obesity continues to rise, affecting increasingly young people. Obesity causes hypertension through a variety of mechanisms, including sympathetic nervous system activation, renin angiotensin aldosterone system, fluid and electrolyte dysregulation, inflammation, and adipokine imbalance. In turn, arterial hypertension can exacerbate obesity by altering metabolic pathways and increasing appetite. The pathophysiological features of hypertension are different between young overweight women and men. We performed a non-systematic literature review to thoroughly investigate mechanisms of pathogenetic interaction and mutual aggravation of high blood pressure and body mass index. The literature was reviewed from 2004 to the present in Russian and English using the PubMed Central, ScienceDirect, Google Scholar platforms, as well as a search in the archives of the journals Circulation and Cardiovascular Therapy and Prevention using the keywords listed below.

Molecular Imaging of Human Brain Organoids Using Mass Spectrometry.

Brain organoid models serve as a powerful tool for studying human brain development and function. Mass spectrometry imaging (MSI), a cutting-edge technology, allows us to map the spatial distribution of diverse molecules such as lipids, sugars, amino acids, drugs, and their metabolites within these organoids, all without the need for specific molecular probes. High-quality MSI data hinge on meticulous sample preparation. Fixatives play a pivotal role, but conventional options such as glutaraldehyde, paraformaldehyde, and cryopreserving such as sucrose may inadvertently impact tissue metabolites. Optimal fixation entails flash freezing in liquid nitrogen. However, for small organoids, a more suitable approach involves transitioning the organoids directly from the incubator into a warmed embedding solution, followed by freezing in dry ice-cooled ethanol. Another critical step is the embedding prior to cryosectioning, which also requires materials compatible with MSI, as traditional options can interfere with matrix deposition and ionization. Here, an optimized protocol for high resolution-MALDI-MSI of human brain organoids is presented, encompassing sample preparation, sectioning, and imaging using mass spectrometry. This method showcases the molecular distribution of small metabolites, such as amino acids, with high mass accuracy and sensitivity. As such, coupled with complementary studies of brain organoids, it can assist in illuminating complex processes governing early brain development, metabolic cell fate trajectories, and distinctive metabolite signatures. Furthermore, it provides insights into the precise locations of molecules within the organoid, enriching our understanding of the spatial organization of 3D brain organoid models. As the field continues to advance, a growing number of studies leveraging MSI to delve into brain organoids and complex biological systems is anticipated, thereby deepening the understanding of the metabolic aspects of human brain function and development.

The Performance of PEFC with Marimo-like Carbon Considering Relative Humidity

A proton exchange membrane fuel cell (PEMFC) is powered by humidified fuel and air gases supplied to the cells. We evaluated the effect of the relative humidity (RH) of the fuel and air gases on the I-V performance of the Marimo-like carbon (MC). MC is a higher order structure of carbon fibers. The RH increased the proton conductivity of the Nafion, while excessive humidification caused flooding. The highest maximum power density was 303 mW cm-2 (80% RH) for the Pt/MC and 165 mW cm-2 (60% RH) for the Pt/CB (carbon black). At all the RHs, the maximum power density of the Pt/MC was higher than that of the Pt/CB. The fiber structure and I/C (0.1) of the MC increase the mass diffusivity of the Pt/MC. The high mass diffusivity of the Pt/MC found to reduce flooding and promote the wetting of the Nafion by the generated water.

Multiband Analysis of Strong Gravitationally Lensed Post-blue Nugget Candidates from the Kilo-degree Survey

During the early stages of galaxy evolution, a significant fraction of galaxies undergo a transitional phase between the “blue nugget” systems, which arise from the compaction of large, active star-forming disks, and the “red nuggets,” which are red and passive compact galaxies. These objects are typically only observable with space telescopes, and detailed studies of their size, mass, and stellar population parameters have been conducted on relatively small samples. Strong gravitational lensing can offer a new opportunity to study them in detail, even with ground-based observations. In this study, we present the first six bona fide samples of strongly lensed post-blue nugget (pBN) galaxies, which were discovered in the Kilo Degree Survey. By using the lensing-magnified luminosity from optical and near-infrared bands, we have derived robust structural and stellar population properties of the multiple images of the background sources. The pBN galaxies have very small sizes of R eff < 1.3 kpc, high mass density inside 1 kpc of log(Σ1/M⊙kpc−2)>9.3 , and low specific star formation rates of log(sSFRGyr-1)≲0 , The size–mass and Σ1–mass relations of this sample are consistent with those of the red nuggets, while their sSFR is close to the lower end of compact star-forming blue nugget systems at the same redshift, suggesting a clear evolutionary link between them.

In-situ observation of defects evolution of graphene nanoflakes in Pt/C catalyst for boosting ORR performance

The structural stability of supported metal nanoparticles determines the activity and longevity of heterogeneous catalysts. Unfortunately, the chemical/thermal working environment inevitably accelerates metal sintering to larger crystallites that leads to the degradation of catalytic performance. Here, we demonstrate that the distribution of defects in carbon support as an inherent parameter plays a crucial role in catalyst sintering. Based on in-situ transmission electron microscopy studies, the strong metal-support interaction between platinum (Pt) nanoparticles and defect-rich graphene nanoflakes largely suppresses metal sintering up to 700 °C. Particularly, the optimal carbon support can be achieved in the annealing process, in which the mass transfer and charge transport can be enhanced by accurately manipulating the distribution of defects in carbon matrix and graphitization degree. It is worth noting that the screened Pt/GNs-300 exhibits impressive oxygen reduction reaction performance with high half-wave potential (0.91 V), mass activity (108.1 A g–1Pt) and excellent stability. By its ascendancy in ORR, the Pt/GNs-300 exhibits a high open-circuit voltage of 1.41 V and a maximum power density of 198.6 mW cm−2 in Zn-air battery, implying its brilliant practicability. This work paves a pathway for achieving sinter-resistant metal-loaded catalysts in energy electrocatalysis.

The Influence of Oat β-Glucans of Different Molar Mass on the Properties of Gluten-Free Bread.

The influence of β-glucans on the properties of gluten-free dough and bread is still not fully explained, with the literature suggesting both positive and negative effects. The aim of this study was to investigate the effect of the molar mass of oat β-glucans on the properties of gluten-free bread. Gluten-free breads were baked under standardized conditions from a model gluten-free mix without and with a 1% or 2% share of oat β-glucans of a low molar mass of 24,540 g/mol, a medium molar mass of 85,940 g/mol and a high molar mass of 1,714,770 g/mol. The share of β-glucans affected the increase in water addition to the baking mix and dough yield proportionally to the molar mass and amount of β-glucans. The β-glucans of the highest molar mass, particularly at a 2% share, were most effective in increasing bread volume, reducing hardness and increasing the moisture content of the bread crumb on the day of baking, as well as reducing the increase in hardness and maintaining a high moisture content of the bread crumb after 1 day of storage, compared to bread without added β-glucans.

Development of Two Novel Dibenzosilole-Based Conjugated Polymers with Thieno[3,4-c]pyrrole-4,6-dione for Use in Polymer Solar Cells

The donor-acceptor (D-A) strategy has proven to be one of the most effective methods for tuning the band gaps, absorption characteristics, and optoelectronic properties in conjugated polymers. Two novel D-A conjugated polymers, PDBSTPD-1T and PDBSTPD-2T, were synthesized using dibenzosilole (DBS) and thieno[3,4-c]pyrrole-4,6-dione (TPD) as the building blocks. These polymers were linked through either a single thiophene or two thiophene rings as π-bridges and were copolymerized using a Suzuki coupling reaction. The effect of the incorporation of the different π-bridges on the electrical/optical properties of the prepared copolymers was also investigated. The synthesized polymers, PDBSTPD-1T and PDBSTPD-2T, were soluble in organic solvents and demonstrated high molar mass along with excellent thermal stability. The conjugation of the electron-accepting TPD unit with the electron-donating DBS unit produced relatively deep HOMO levels, which were fine-tuned to be −5.44 and −5.36 eV via the addition of the different π-bridges. PDBSTPD-1T and PDBSTPD-2T displayed absorption wavelengths between 350 and 650 nm with high Eg opt of 2.01 and 1.97 eV, respectively. X-ray diffraction analysis presented several diffraction peaks, and the π-π stacking distances of PDBSTPD-1T and PDBSTPD-2T were 3.45 and 3.65°A, respectively.

Synergistic Regulation of Anode and Cathode Interphases via an Alum Electrolyte Additive for High-Performance Aqueous Zinc-Vanadium Batteries.

A zinc (Zn) metal anode paired with a vanadium oxide (VOx) cathode is a promising system for aqueous Zn-ion batteries (AZIBs); however, side reactions proliferating on the Zn anode surface and the infinite dissolution of the VOx cathode destabilise the battery system. Here, we introduce a multi-functional additive into the ZnSO4 (ZS) electrolyte, KAl(SO4)2 (KASO), to synchronise the in situ construction of the protective layer on the surface of the Zn anode and the VOx cathode. Theoretical calculations and synchrotron radiation have verified that the high-valence Al3+ plays dual roles of competing with Zn2+ for solvation and forming a Zn-Al alloy layer with a homogeneous electric field on the anode surface to mitigate the side reactions and dendrite generation. The Al-containing cathode-electrolyte interface (CEI) considerably alleviates the irreversible dissolution of the VOx cathode and the accumulation of byproducts. Consequently, the Zn||Zn cell with KASO exhibits an ultra-long cycle of 6000 h at 2 mA cm-2. Importantly, the VOx cathodes (VO2, V2O5 and NH4V4O10) in the ZS-KASO electrolyte showed excellent cycling stability, including Zn powder||VO2 cells and Zn||VO2 pouch cells. Even better, the full cell exhibits excellent cycling stability at low negative/positive (N/P) ratio of 2.83 and high mass loading (~16 mg cm-2). This study offers a straightforward and practical reference for concurrently addressing challenges at the anode and cathode of AZIBs.

LC-HRMS Analysis of Abelmoschus Manihot Medik from Palu of Central Sulawesi

Abelmoschus manihot (L.) Medik is one of the traditional medicinal plants from Palu City, Central of Sulawesi with the Malvaceae plant family and commonly is a traditional medicinal plants recognized fot its therapeutic potential, particularly in antioxidant, anti-inflammatory and wound healing applications. This research aims to identify and characterize the chemical compounds present in Abelmoschus manihot (L.) Medik plant from Palu City, Central of Sulawesi using liquid chromatography high resolution mass spectrometry (LC-HRMS). This research was collected fresh plant, designed using ethanol extraction from Abelmoschus manihot (L.) Medik and analyzed using mass spectroscopy (LC-HRMS) with Processing Software – MZMine Ver. 3.9.0. The results of this study provide new insights into the chemical composition of Abelmoschus manihot (L.) Medik and confirm its potential as a source of bioactive compounds that could be futher explored for pharmaceutical development, namely that it contains the main compound Quercetin with a mass of 303.04, Gossypetin; Myricetin with a mass of 319.04, Quercetin 3-O-alpha-L-rhamnoside with a mass of 449.10 Isoquercetin; Hyperoside; Hyperin; Hirsutrin with a mass of 465.10, Gossypol with a mass of 519.20 and rutin with a mass of 291.08.

Metabolomic profiling of colostrum bar for identification of functional compounds using high resolution mass spectroscopy

Metabolomic profiling of colostrum bar for identification of functional compounds using high resolution mass spectroscopy

Fate of per- and polyfluoroalkyl substances at a 40-year dedicated municipal biosolids land disposal site

The fate of per- and polyfluoroalkyl substances (PFAS) was evaluated at a site where municipal biosolids have been applied annually for 38 years as a waste management strategy. Soil cores (1.8 m in 30-cm sections), groundwater from four wells, and biosolids applied in 2022 were analyzed for PFAS (54 targeted, 17 semi-quantified) using liquid chromatography high resolution mass spectrometry including suspect screening. Total PFAS concentrations decreased with soil depth from 1700 ng/g to 2.06 ng/g. PFAS distribution in 2022 biosolids were 60 mol% perfluoroalkyl acid (PFAA) precursors and intermediates. The surface soil was dominated by long-chain PFAAs (67–76 mol%) reflecting precursor degradation after biosolids application. Presence of semi-quantified intermediates further reflects precursor degradation in surface soil. Long-chain PFAAs diminished with depth while short-chain PFAAs increased with up to 98 and 96 mol% short-chain PFAAs in the bottom depth and groundwater, respectively. PFAS distribution with depth is consistent with chain-length dependent sorption-impacted transport and the high organic carbon content of the surface soil (15.2 % OC) which subsequently decreased with depth (~2–3 % OC at >60 cm). High organic carbon content in the upper horizon is likely from decades of high biosolids application rates, which contributed to minimizing leaching of long-chain PFAS. While the well within the dedicated land disposal is not drinking water, for comparison only, PFAS concentrations in this well only marginally exceeded the EU drinking water directive for total PFAS and a few individual short-chain PFAS, but did exceed tenfold, the USEPA drinking water standard for PFOA.

The Orbit and Companion of PSR J1622-0315: Variable Asymmetry and a Massive Neutron Star

The companion to PSR J1622-0315, one of the most compact known redback millisecond pulsars, shows extremely low irradiation despite its short orbital period. We model this system to determine the binary parameters, combining optical observations from the New Technology Telescope in 2017 and the Nordic Optical Telescope in 2022 with the binary modeling code ICARUS. We find a best-fit neutron star mass of 2.3 ± 0.4 M ⊙, and a companion mass of 0.15 ± 0.02 M ⊙. We detect for the first time low-level irradiation from asymmetry in the minima as well as a change in the asymmetry of the maxima of its light curves over five years. Using starspot models, we find better fits than those from symmetric direct heating models, with consistent orbital parameters. We discuss an alternative scenario where the changing asymmetry is produced by a variable intrabinary shock. In summary, we find that PSR J1622-0315 combines low irradiation with variable light-curve asymmetry and a relatively high neutron star mass.

Burden of disease attributable to high body mass index: an analysis of data from the Global Burden of Disease Study 2021

Obesity represents a major global health challenge with important clinical implications. Despite its recognized importance, the global disease burden attributable to high body mass index (BMI) remains less well understood. We systematically analyzed global deaths and disability-adjusted life years (DALYs) attributable to high BMI using the methodology and analytical approaches of the Global Burden of Disease Study (GBD) 2021. High BMI was defined as a BMI over 25kg/m2 for individuals aged ≥20 years. The Socio-Demographic Index (SDI) was used as a composite measure to assess the level of socio-economic development across different regions. Subgroup analyses considered age, sex, year, geographical location, and SDI. From 1990 to 2021, the global deaths and DALYs attributable to high BMI increased more than 2.5-fold for females and males. However, the age-standardized death rates remained stable for females and increased by 15.0% for males. Similarly, the age-standardized DALY rates increased by 21.7% for females and 31.2% for males. In 2021, the six leading causes of high BMI-attributable DALYs were diabetes mellitus, ischemic heart disease, hypertensive heart disease, chronic kidney disease, low back pain and stroke. From 1990 to 2021, low-middle SDI countries exhibited the highest annual percentage changes in age-standardized DALY rates, whereas high SDI countries showed the lowest. The worldwide health burden attributable to high BMI has grown significantly between 1990 and 2021. The increasing global rates of high BMI and the associated disease burden highlight the urgent need for regular surveillance and monitoring of BMI. National Natural Science Foundation of China and National Key R&D Program of China.

Exploring the characteristics changes of cardiopulmonary exercise testing in patients with acute coronary syndrome after PCI before and during the COVID-19 pandemic

Objective: To investigate the changes in cardiopulmonary exercise testing (CPET) characteristics before and after the outbreak of COVID-19 in patients with acute coronary syndrome (ACS) who underwent percutaneous coronary intervention (PCI). Methods: This is a cross-sectional study that included ACS patients who underwent PCI at the General Hospital of the Northern Theater Command from July 2018 to February 2023. Based on the timeline of the COVID-19 pandemic, patients were divided into two groups: the pre-pandemic group and the during-pandemic group, with January 2020 as the dividing line. Clinical data were collected from both groups, and a comparative analysis was performed on their postoperative CPET outcomes, including peak oxygen uptake (peak VO2), peak metabolic equivalents (peak MET), and other indicators. Weber's classification was used to assess cardiac function. In addition, the 7-tiem generalized anxiety disorder scale (GAD-7) and the patient health questionnaire-9 (PHQ-9) were used to assess the patients' psychological anxiety and depression states, respectively. Multivariate logistic regression was used to analyze the influencing factors of CPET after PCI. Results: A total of 4 310 post-PCI ACS patients were included, with an average age of (58.7±9.1) years, and 3 464 (80.37%) were male. There were 1 698 patients in the pre-pandemic group and 2 612 patients in the during-pandemic group. The main indicator of the CPET, peak VO2 (15.04±3.93) ml·min-1·kg-1 in the during-pandemic group, was lower than that in the pre-pandemic group (15.52±3.68) ml·min-1·kg-1, and the difference was statistically significant (P<0.001). Multivariate logistic regression analysis showed that advanced age, female gender, high body mass index, elevated high-sensitivity C-reactive protein, reduced high-density lipoprotein cholesterol, smoking history, history of myocardial infarction, more severe ACS classification, and mild to moderate degree of depression were related to poor cardiopulmonary outcomes (P<0.05). Conclusion: The COVID-19 pandemic had a negative impact on the cardiopulmonary outcomes of ACS patients after PCI. Reduced physical activity, and increased psychological stress should be given consideration and attention regarding their impact on patients' cardiopulmonary function.

High-performance liquid chromatography-tandem mass spectrometry was used to measure 20 antidepressants in human serum.

Aim: This study used high performance liquid chromatography-tandem mass spectrometry to quantify the blood concentrations of 20 antidepressants, such as bupropion and fluoxetine, in human serum samples.Methods: After direct precipitation with a 1:9 protein precipitant of methanol and acetonitrile, serum samples were examined using high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS). The material was separated using a Poroshell 120 EC-C18 column (3.0mm×50mm, 2.7μm) and gradient elution. The mobile phases were phase A 0.01% formic acid aqueous solution (containing 2mmol/ml ammonium acetate) and phase B methanol solution. A 0.45ml/min flow rate was used to divide the sample and inject 5μl. Electrospray ionization source positive ion mode and multiple reaction monitoring modes were used for analysis. Measurement was quantified using an internal standard technique.Results: Accuracy ranged from 90.3 to 114.3%, intra-day precision from 100.1 to 112.3%, inter-day precision from 100.4 to 112.6%, extraction recoveries from 85.5 to 114.5% and matrix effect from 85.6 to 98.7%.Conclusion: This approach is fast, accurate, sensitive and repeatable. It can identify 20 antidepressants in blood simultaneously. This can be used to monitor blood drug levels and medication metabolism.

Homogeneous continuous flow nitration of O-methylisouronium sulfate and its optimization by kinetic modeling.

Nitration of O-methylisouronium sulfate under mixed acid conditions gives O-methyl-N-nitroisourea, a key intermediate of neonicotinoid insecticides with high application value. The reaction is a fast and highly exothermic process with a high mass transfer resistance, making its control difficult and risky. In this paper, a homogeneous continuous flow microreactor system was developed for the nitration of O-methylisouronium sulfate under high concentrations of mixed acids, with a homemade static mixer eliminating the mass transfer resistance. In addition, the kinetic modeling of this reaction was performed based on the theory of NO2 + attack, with the activation energy and pre-exponential factor determined. Finally, based on the response surface generated by the kinetic model, the reaction was optimized with a conversion of 87.4% under a sulfuric acid mass fraction of 94%, initial reactant concentration of 0.5 mol/L, reaction temperature of 40 °C, molar ratio of reactants at 4.4:1, and a residence time of 12.36 minutes.