Online Compositional Analysis of Complex Oligomers in Biomass Degradation by High-Pressure Flow-Through Reactor Coupled with High-Resolution Mass Spectrometry.

Online analysis of the composition and evolution of complex oligomeric intermediates in biomass degradation is highly desirable to elucidate the mechanism of bond cleavage and study the effect of conditions on the selective conversion of feedstocks. However, harsh reaction conditions and complicated conversion systems pose tremendous challenges for conventional, state-of-the-art analytical techniques. Herein, we introduce a continuous and rapid compositional analysis strategy coupling a high-pressure flow-through reactor with online high-resolution mass spectrometry, which enables the molecular-level characterization of most biomass-related products throughout the conversion for over 2 h. Catalytic depolymerization of one model compound was studied, and temperature-dependent data of over 50 intermediates as well as recondensation dimers and oligomers were obtained, which have rarely been reported in the literature. Thousands of products during the flow-through conversion of birch wood with molecular weights up to 1000 Da were presented, and 8 typical lignin dimers and oligomers with various interunit linkages were identified at the molecular level, demonstrating the potential to analyze more complicated systems far beyond conventional methods, especially for complex oligomers. The continuous evolutions of different components and typical products were unveiled for the first time, providing valuable insights into the investigation of the structure, composition, and decomposition mechanism of lignocellulose as well as the influence of reaction conditions. This method leads to the previously unattained ability to probe and reveal complicated chemical compositions in high-pressure reactions and can be applied to all other high-pressure heterogeneous aqueous reactions.

AP-HTPB propellant combustion under strain conditions with laser absorption spectroscopy.

Understanding the combustion behaviors of solid propellant with different levels of strains is of practical interest. In this work, an experimental study of the effects of static and dynamic strains on the burning rate, temperature, CO, and C O 2 formation of aluminized ammonium perchlorate (AP)-hydroxyl terminated poly-butadiene (HTPB) propellant combustion was presented at initial pressures of 0.1 MPa, 0.2 MPa, and 0.5 MPa. The strains were being applied onto solid propellant by exerting static and cyclic loadings. The propellant burning rate was acquired by a 4 kHz high-speed photography system, and the combustion temperature, CO, and C O 2 column densities were measured at 10 kHz through laser absorption spectroscopy (LAS). At atmospheric pressure, it was demonstrated that the propellant burning rate increased with tensile stress and decreased with compressive stress. The measured flame temperature showed a similar correlation with strains as compared to the propellant burning rate. At elevated pressures, the increase of the propellant burning rate due to tensile stress was more evident, while the difference in combustion temperatures was less significant. For the cyclic strain condition, the variations of the measured C O 2 and CO column densities were consistent with the static strain condition.

A Mechanistic Study of HZSM-5-Catalyzed Guaiacol Amination Using Photoionization Time-of-Flight Mass Spectrometry.

Thermal-catalytic conversion and amination (TCC-A) of lignin and lignin derivates over zeolites is a promising and renewable method to produce aromatic amines, but suffers from product diversity. Currently, no unambiguous mechanism could fully describe the chemistry of this process. In this work, the TCC-A mechanism of guaiacol, a typical lignin model compound, with ammonia over HZSM-5 was investigated by online photoionization time-of-flight mass spectrometry combined with density functional theory. Various products including amines, pyrroles, and pyridines were identified. The formation of methylamine and aminophenol below 400 °C via nucleophilic substitutions is attributed to the strong adsorption of ammonia on the active site of HZSM-5. Aniline is the major product above 400 °C coproduced with pyrroles and pyridines. It is suggested that the reactions among radical intermediates (•CH3 and •NH2) and molecules (guaiacol and catechol) lead to poor aniline selectivity via transmethylation, amination, and partial deoxygenation reactions. Hydroamination is proposed as the main formation mechanism of pyrroles and pyridines. The maximum yield of aniline can be achieved at 650 °C owing to the enhancement of amination and deoxygenation and the suppression of transmethylation reactions.

Probing combustion and catalysis intermediates by synchrotron vacuum ultraviolet photoionization molecular-beam mass spectrometry: recent progress and future opportunities.

Soft photoionization molecular-beam mass spectrometry (PI-MBMS) using synchrotron vacuum ultraviolet (SVUV) light has been significantly developed and applied in various fields in recent decades. Particularly, the tunability of SVUV light enables two-dimensional measurements, i.e. mass spectrum and photoionization efficiency spectrum measurements, affording isomer distinguishment in complex reaction processes. Many key intermediates have been successfully detected in combustion and catalysis reactions with the help of the state-of-the-art SVUV-PI-MBMS, promoting the understanding of the chemical mechanisms. Herein, we present a brief review of the instrumentation of beamline and PI-MBMS machines at the current synchrotron user facility Hefei Light Source II and exemplify the advantages of the SVUV-PI-MBMS method with recent applications in combustion and catalysis research, especially in probing key reaction intermediates. Future opportunities with the next generation synchrotron light source and bench-top light source have also been discussed.

Role of formaldehyde in promoting aromatic selectivity during methanol conversion over gallium-modified zeolites.

Gallium-modified HZSM-5 zeolites are known to increase aromatic selectivity in methanol conversion. However, there are still disputes about the exact active sites and the aromatic formation mechanisms over Ga-modified zeolites. In this work, in situ synchrotron radiation photoionization mass spectrometry (SR-PIMS) experiments were carried out to study the behaviors of intermediates and products during methanol conversion over Ga-modified HZSM-5. The increased formaldehyde (HCHO) yield over Ga-modified HZSM-5 was found to play a key role in the increase in aromatic yields. More HCHO was deemed to be generated from the direct dehydrogenation of methanol, and Ga2O3 in Ga-modified HZSM-5 was found to be the active phase. The larger increase in aromatic production over Ga-modified HZSM-5 after reduction‒oxidation treatment was found to be the result of redispersed Ga2O3 with smaller size generating a larger amount of HCHO. This study provides some new insights into the internal driving force for promoting the production of aromatics over Ga-modified HZSM-5.

In Situ Reactor-Integrated Electrospray Ionization Mass Spectrometry for Heterogeneous Catalytic Reactions and Its Application in the Process Analysis of High-Pressure Liquid-Phase Lignin Depolymerization.

Process analysis of heterogeneous catalytic reactions such as lignin depolymerization is essential to understand the reaction mechanism at the molecular level, but it is always challenging due to harsh conditions. Herein, we report an operando process analysis strategy by combining a microbatch reactor with high-resolution mass spectrometry (MS) via a reactor-integrated electrospray ionization (R-ESI) technique. R-ESI-MS expands the applications of traditional in situ MS to a heterogeneous and high-pressure liquid-phase system. With this strategy, we present the evolution of a series of monomers, dimers, and oligomers during lignin depolymerization under operando conditions (methanol solvent, 260 °C, ∼8 MPa), which is the first experimental elucidation of a progressive depolymerization pathway and evidence of repolymerization of active monomers. The proposed R-ESI-MS is crucial in probing depolymerization intermediates of lignin; it also provides a flexible strategy for process analysis of heterogeneous catalytic reactions under operando conditions.

Continuous Butadiyne Addition to Propargyl: A Radical-Efficient Pathway for Polycyclic Aromatic Hydrocarbons.

Polycyclic aromatic hydrocarbons (PAHs) play a crucial role in soot inception, interstellar evolution, and nanomaterial synthesis. Although several mechanisms, such as hydrogen-abstraction acetylene/vinylacetylene addition, have previously been proposed, PAH formation and growth are not yet fully understood. We propose an alternate PAH growth mechanism wherein propargyl radical reacts with butadiyne to form larger radicals containing newly fused aromatic rings. Butadiyne is an important intermediate in hydrocarbon oxidation and carbon rich stars, while propargyl is one of the most important resonantly stabilized radicals that persists for long times. Our proposed mechanism is validated by quantum chemical calculations, elementary reaction experiments, laminar flame analysis, and kinetic modeling. Our findings challenge the conventional wisdom that radical site regeneration, being central to PAH growth, requires sequential hydrogen elimination and/or abstraction. In our proposed mechanism, PAH growth does not depend on abundant free radical consumption, and could, therefore, help explain carbonaceous nanoparticle coalescence in radical-deficient reaction environments.

Online investigation on catalytic co-pyrolysis of cellulose and polyethylene over magnesium oxide by advanced mass spectrometry.

Due to rapid deactivation of catalysts, the effective conversion of biomass with oxygen-rich and hydrogen-deficient characteristics to transportation fuels and high-valued chemicals via catalytic pyrolysis remains a challenge for commercialization. Hydrogen-rich plastic is used as feedstock co-fed with biomass to improve the catalytic pyrolysis process. The present work aims to investigate the co-pyrolysis process of cellulose and polyethylene (PE) over MgO by TG combined with photoionization time-of-flight mass spectrometry (PI-TOF-MS), which features on-line detection of catalytic pyrolysis products in real time. The MgO catalyst could improve the pyrolysis of cellulose and enhance the CC bond breaking of PE, respectively. During catalytic co-pyrolysis, the yields from olefins and furan as well as its derivatives can be enhanced obviously. Further, the formation of additional aromatics can be observed due to the Diels-Alder reaction. This work shows TG coupled to PI-TOF-MS is a powerful setup to study and optimize catalytic co-pyrolysis process.

Insights into the Decomposition and Oxidation Chemistry of p-Xylene in Laminar Premixed Flames.

This work reports an experimental and kinetic modeling investigation on laminar premixed flame of p-xylene at 0.04 atm and equivalence ratios of 0.75, 1.0, and 1.79. Intermediates such as the p-xylyl radical, p-xylylene, and styrene, as well as polycyclic aromatic hydrocarbons (PAHs), were detected by using synchrotron vacuum ultraviolet photoionization mass spectrometry. Based on our previous aromatic kinetic model, a detailed kinetic model of p-xylene combustion was developed, and the model was validated against the present flame structure data. Model analysis work was also performed in order to reveal the important reactions in p-xylene decomposition and oxidation. The H-abstraction reactions leading to the p-xylyl radical are found to control the consumption of p-xylene in all the three flames. In the rich flame, p-xylyl mainly suffers the H-elimination and isomerization reactions, which produce p-xylylene and the o-xylyl radical, respectively. The further decomposition reactions of the o-xylyl radical contribute to the production of styrene, which is another important C8 intermediate observed in the rich flame. In the stoichiometric and lean flames, p-xylyl mainly suffers the oxidation reactions by O, which give p-methylbenzaldehyde as major product. The growth pathways of PAHs in the rich flame were also investigated in this work. Indenyl, indene, naphthalene, and phenanthrene were observed as the abundantly produced bicyclic and tricyclic PAHs due to the existence of direct formation pathways from the decomposition of p-xylyl radical.

Evidence of a Phenolic Pool as a Key Intermediate for Zeolite-Catalyzed Lignin Pyrolysis.

The phenolic pool is considered to be an important intermediate during the catalytic conversion of biomass. However, no direct evidence has been reported on its full picture on a molecular level due to the huge challenges in probing the reactive and lowly volatile phenolic oligomers with state-of-the-art technologies. Herein, we report the online detection and structural identification of a phenolic pool by utilizing in-situ atmospheric-pressure photoionization mass spectrometry, demonstrating that the phenolic pool is formed through repolymerization of monomers with an equidistant group pattern and acts as a key mechanistic step for both valuable aromatic products and undesired coke. The exploration of the real reactive species is also of great importance for the rational design and synthesis of advanced catalysts with high activity.

Formation and Fate of Formaldehyde in Methanol-to-Hydrocarbon Reaction: In Situ Synchrotron Radiation Photoionization Mass Spectrometry Study.

HCHO has been confirmed as an active intermediate in the methanol-to-hydrocarbon (MTH) reaction, and is critical for interpreting the mechanisms of coke formation. Here, HCHO was detected and quantified during the MTH process over HSAPO-34 and HZSM-5 by in situ synchrotron radiation photoionization mass spectrometry. Compared with conventional methods, excellent time-resolved profiles were obtained to study the formation and fate of HCHO, and other products during the induction, steady-state reaction, and deactivation periods. Similar formation trends of HCHO and methane, and their close correlation in yields suggest that they are derived from disproportionation of methanol at acidic sites. In the presence of Y2 O3 , the amount of HCHO changes, affecting the hydrogen-transfer processes of olefins into aromatics and aromatics into cokes. The yield of HCHO affects the aromatic-based cycle and the formation of ethylene, indicating that ethylene is mainly formed from the aromatic-based cycle.

In Situ Atmospheric Pressure Photoionization Mass Spectrometric Monitoring of Initial Pyrolysis Products of Biomass in Real Time.

Knowledge on the initial and intermediate pyrolysis products of biomass is essential for the mechanistic investigation of biomass pyrolysis and further optimization of upgrading processes. The conventional method can only detect the final products, which do not resemble the initial or intermediate pyrolysis products. Here, we introduce a direct orifice sampling combined with atmospheric pressure photoionization mass spectrometry (APPI-MS) for in situ online analysis of the evolved volatile initial products from the pyrolysis of biomass. Pyrolysis experiments of both dimeric model compound (guaiacylglycerol-ß-guaiacyl ether, GGGE) and poplar wood were carried out to validate the generality of the method. Generally, secondary reactions can be reduced by shortening the distance between the sample and sampling orifice. Large molecular-weight initial products up to trimers were detected during the pyrolysis of poplar wood, and no initial products larger than trimers were detected. It is inferred that in situ APPI immediately after sample extraction ensures efficient and effective product detection. Furthermore, the present work offers a promising feasible method for online tracing of reaction intermediates not only in pyrolysis but also in various reactive processes (e.g., catalytic reaction, oxidation) under operando conditions.

Study of the thermal decomposition mechanism of FOX-7 by molecular dynamics simulation and online photoionization mass spectrometry.

The thermal decomposition mechanism of energetic materials is important for analyzing the combustion mechanisms of propellants and evaluating the safety of propellants during transport and storage. 1,1-Diamino-2,2-dinitroethylene (FOX-7) is an important insensitive energetic material that can be used as an oxidizer in propellants. However, the initial decomposition mechanism of FOX-7 is not clear to date. The ReaxFF molecular dynamics method is widely used in the investigation of the thermal decomposition mechanisms of energetic materials. Meanwhile, the combination of thermogravimetry with online photoionization time-of-flight mass spectrometry (TG-PI-TOF-MS) and online single-photon ionization time-of-flight mass spectrometry (SPI-TOF-MS) can reveal the decomposition products, which may be integrated with the results of the simulation. In this study, the primary thermal decomposition mechanism of 1,1-diamino-2,2-dinitroethylene (FOX-7) was studied by the ReaxFF molecular dynamics simulations and online photoionization mass spectrometry. The results of the molecular dynamics simulations showed that the primary decomposition step of FOX-7 is C-NO2 cleavage; after this, C[double bond, length as m-dash]O formation occurs via a three-membered ring transition state, followed by NO elimination. The remaining structure loses NH2 and H, resulting in the formation of the NHC[double bond, length as m-dash]C[double bond, length as m-dash]O structure, which finally breaks down into HNC and CO. NH2 reacts with an H atom to produce NH3. A reversible intramolecular hydrogen transfer was also observed at 2500 K; however, it failed to dominate the decomposition reaction. During the decomposition of FOX-7, the major products are N2, NH3, CO2, and H2N2 and the minor products are H2O, HN2, and H2. The TG-PI-TOF-MS spectrum shows three signals, i.e., m/z = 18, 28, and 30, which can be assigned to H2O, CO, and NO, respectively. Moreover, four signals at m/z = 72.72, 55.81, 45.79, and 29.88 corresponding to the products (NH2)2C[double bond, length as m-dash]C[double bond, length as m-dash]O, (NH2)C[double bond, length as m-dash]C[double bond, length as m-dash]O, NO2, and NO have been obtained in the SPI-TOF-MS spectrum. The experimental data obtained via online photoionization mass spectrometry further validated the results of the molecular dynamics simulations.

Online photoionization mass spectrometric evaluation of catalytic co-pyrolysis of cellulose and polyethylene over HZSM-5.

The hydrogen-deficient and oxygen-rich nature of lignocellulosic biomass prohibits effective conversions of biomass to fuels and chemicals via catalytic pyrolysis due to significant coking of the catalysts. Co-feeding of biomass feedstock with hydrogen-rich and oxygen-deficient thermoplastics could improve the process. Herein, thermal and catalytic co-pyrolysis of cellulose and polyethylene (PE) was studied via thermogravimetry combined with an online photoionization time-of-flight mass spectrometry (PI-TOF-MS). No notable synergetic effect was found in the thermal co-pyrolysis process while a considerable synergetic effect was observed during the catalytic co-pyrolysis. In the case of catalytic pyrolysis, co-feeding of cellulose with PE significantly improved the aromatic formation. Detailed reaction intermediates and products were detected by PI-TOF-MS and the process of aromatization could be ascribed to aromatization of small oxygenates and olefins, as well as Diels-Alder reaction and dehydration by HZSM-5. Moreover, this study provides a reliable tool for screening and optimizing of catalytic co-pyrolysis.

Note: Possibilities of detecting the trace-level erosion products from an electric propulsion hollow cathode plasma source by the method of time-of-flight mass spectrometry.

A hollow cathode produces electrons which neutralize ions from electric propulsion thrusters. After hundreds to thousands of hours of operation in space, the cathode materials can be significantly eroded due to ion bombardment. As a result, the electric propulsion system performance will be obviously changed or even fail. In this work, the erosion products from a LaB6 hollow cathode (widely used presently in electric propulsion systems) are studied by using a specific detection system, which consists of a molecular beam sampler and a time-of-flight mass spectrometer. This system measures trace-level-concentration (10-6-10-3) products. Boron (B), tantalum (Ta), and tungsten (W)-originating from the emitter, keeper, and orifice of the hollow cathode-are measured. It is found that the erosion rate is significantly influenced by the gas flow rate to the cathode.

Extractive Atmospheric Pressure Photoionization (EAPPI) Mass Spectrometry: Rapid Analysis of Chemicals in Complex Matrices.

Extractive atmospheric pressure photoionization (EAPPI) mass spectrometry was designed for rapid qualitative and quantitative analysis of chemicals in complex matrices. In this method, an ultrasonic nebulization system was applied to sample extraction, nebulization, and vaporization. Mixed with a gaseous dopant, vaporized analytes were ionized through ambient photon-induced ion-molecule reactions, and were mass-analyzed by a high resolution time-of-flight mass spectrometer (TOF-MS). After careful optimization and testing with pure sample solution, EAPPI was successfully applied to the fast screening of capsules, soil, natural products, and viscous compounds. Analysis was completed within a few seconds without the need for preseparation. Moreover, the quantification capability of EAPPI for matrices was evaluated by analyzing six polycyclic aromatic hydrocarbons (PAHs) in soil. The correlation coefficients (R (2) ) for standard curves of all six PAHs were above 0.99, and the detection limits were in the range of 0.16-0.34 ng/mg. In addition, EAPPI could also be used to monitor organic chemical reactions in real time. Graphical Abstract ᅟ.

The vacuum ultraviolet beamline/endstations at NSRL dedicated to combustion research.

An undulator-based vacuum ultraviolet (VUV) beamline (BL03U), intended for combustion chemistry studies, has been constructed at the National Synchrotron Radiation Laboratory (NSRL) in Hefei, China. The beamline is connected to the newly upgraded Hefei Light Source (HLS II), and could deliver photons in the 5-21 eV range, with a photon flux of 10(13) photons s(-1) at 10 eV when the beam current is 300 mA. The monochromator of the beamline is equipped with two gratings (200 lines mm(-1) and 400 lines mm(-1)) and its resolving power is 3900 at 7.3 eV for the 200 lines mm(-1) grating and 4200 at 14.6 eV for the 400 lines mm(-1) grating. The beamline serves three endstations which are designed for respective studies of premixed flame, fuel pyrolysis in flow reactor, and oxidation in jet-stirred reactor. Each endstation contains a reactor chamber, an ionization chamber where the molecular beam intersects with the VUV light, and a home-made reflectron time-of-flight mass spectrometer. The performance of the beamline and endstations with some preliminary results is presented here. The ability to detect reactive intermediates (e.g. H, O, OH and hydroperoxides) is advantageous in combustion chemistry research.

Selective conversion of syngas to light olefins.

Although considerable progress has been made in direct synthesis gas (syngas) conversion to light olefins (C2(=)-C4(=)) via Fischer-Tropsch synthesis (FTS), the wide product distribution remains a challenge, with a theoretical limit of only 58% for C2-C4 hydrocarbons. We present a process that reaches C2(=)-C4(=) selectivity as high as 80% and C2-C4 94% at carbon monoxide (CO) conversion of 17%. This is enabled by a bifunctional catalyst affording two types of active sites with complementary properties. The partially reduced oxide surface (ZnCrO(x)) activates CO and H2, and C-C coupling is subsequently manipulated within the confined acidic pores of zeolites. No obvious deactivation is observed within 110 hours. Furthermore, this composite catalyst and the process may allow use of coal- and biomass-derived syngas with a low H2/CO ratio.

Ultrasonic nebulization extraction/low pressure photoionization mass spectrometry for direct analysis of chemicals in matrices.

A novel ultrasonic nebulization extraction/low-pressure photoionization (UNE-LPPI) system has been designed and employed for the rapid mass spectrometric analysis of chemicals in matrices. An ultrasonic nebulizer was used to extract the chemicals in solid sample and nebulize the solvent in the nebulization cell. Aerosols formed by ultrasonic were evaporated by passing through a transferring tube, and desolvated chemicals were ionized by the emitted light (10.6 eV) from a Krypton discharge lamp at low pressure (∼68 Pa). First, a series of semi/non-volatile compounds with different polarities, such as polycyclic aromatic hydrocarbons (PAHs), amino acids, dipeptides, drugs, nucleic acids, alkaloids, and steroids were used to test the system. Then, the quantification capability of UNE-LPPI was checked with: 1) pure chemicals, such as 9,10-phenanthrenequinone and 1,4-naphthoquinone dissolved in solvent; 2) soil powder spiked with different amounts of phenanthrene and pyrene. For pure chemicals, the correlation coefficient (R(2)) for the standard curve of 9,10-phenanthrenequinone in the range of 3 ng-20 µg mL(-1) was 0.9922, and the measured limits of detection (LOD) was 1 ng ml(-1). In the case of soil powder, linear relationships for phenanthrene and pyrene from 10 to 400 ng mg(-1) were obtained with correlation coefficients of 0.9889 and 0.9893, respectively. At last, the feasibility of UNE-LPPI for the detection of chemicals in real matrices such as tablets and biological tissues (tea, Citrus aurantium peel and sage (Salvia officinalis) leaf) were successfully demonstrated.

A field-programmable-gate-array based time digitizer for the time-of-flight mass spectrometry.

The time-of-flight (TOF) mass spectrometry is one of the most widely used techniques to get information about the composition and structure of compounds. The time digitizer, based on time-to-digital conversion, is one of the important parts in modern TOF mass spectrometry, which is often implemented with analog circuitry or application-specific-integrated-circuit (ASIC) devices. However, it is difficult to achieve a high density with the analog approach. Furthermore, ASIC requires a long design cycle and the function cannot be easily revised for different applications. In this work, we present a highly flexible, accurate, yet low-costing design of time digitizer which is based on a field-programmable-gate-array (FPGA) and time interpolation method. Test results indicate that the bin size of this time digitizer is 390 ps with an average standard deviation (about 150 ps). The differential nonlinearity is in the range of -0.10 to +0.05 LSB (least significant bit), and the measurement time range is larger than 107 s. Compared with other techniques, it reduces the system complexity while providing a good flexibility. In addition, this technique can also accommodate one or more STOP pulse measurements for each START pulse reference, enabling measurement of multiple times-of-flight with a common start trigger. Besides, a time stamp is recorded for each input pulse, rendering this time digitizer versatile in other applications. Moreover, because of the programmable characteristic of a FPGA, more functions can be integrated in the time digitizer, such as a trigger function, data transfer interface; the parameters such as the number of the channels. The measurement range can also be modified according to different requirements.