Xuejun Gu

Direct detection of isoprene photooxidation products by using synchrotron radiation photoionization mass spectrometry.

We report the combination of a vacuum ultraviolet photoionization mass spectrometer, operating on the basis of synchrotron radiation, with an environmental reaction smog chamber for the first time. The gas- and pseudo-particle-phase products of OH-initiated isoprene photooxidation reactions were measured on-line and off-line, respectively, by mass spectrometry. It was observed that aldehydes, methacrolein, methyl vinyl ketone, methelglyoxal, formic acid, and similar compounds are the predominant gas-phase photooxidation products, whereas some multifunctional carbonyls and acids mainly exist in the particle phase. This finding is reasonably consistent with results of studies conducted in other laboratories using different methods. The results indicate that synchrotron radiation photoionization mass spectrometry coupled with a smog chamber is a potentially powerful tool for the study of the mechanism of atmospheric oxidations and the formation of secondary organic aerosols.

Size distribution and chemical composition of secondary organic aerosol formed from Cl-initiated oxidation of toluene

Secondary organic aerosol (SOA) formed from C1-initiated oxidation of toluene was investigated in a home-made smog chamber. The size distribution and chemical composition of SOA particles were measured using aerodynamic particle sizer spectrometer and the aerosol laser time-of-flight mass spectrometer (ALTOFMS), respectively. According to a large number of single aerosol diameter and mass spectra, the size distribution and chemical composition of SOA were obtained statistically. Experimental results showed that SOA particles created by C1-initiated oxidation of toluene is predominantly in the form of fine particles, which have diameters less than 2.5 microm (i.e., PM2.5), and glyoxal, benzaldehyde, benzyl alcohol, benzoquinone, benzoic acid, benzyl hydroperoxide and benzyl methyl nitrate are the major products components in the SOA. The possible reaction mechanisms leading to these products are also proposed.

Experimental study of particulate products for aging of 1,3,5–trimethylbenzene secondary organic aerosol

Secondary organic aerosol (SOA) from the photooxidation of aromatic compounds is a very complex mixture containing products with a different chemical nature that are dependent on aging processes. In this study, we focus on the chemical characterization of major products that are formed from the OH–initiated oxidation of 1,3,5–trimethylbenzene and subsequent aging through OH–initiated reactions in the presence of NOx.The chemical composition of aged particles were measured in real–time by an aerosol laser time of flight mass spectrometer (ALTOFMS) coupled with Fuzzy C–Means (FCM) clustering algorithm. Experimental results demonstrated that methyl glyoxylic acid, 2–methyl–4–oxo–2–pentenoic acid, 3,5–dimethylbenzoic acid, 2–methyl–2,3–dihydroxyl–4–oxo–pentanoic acid, dimethyl–nitrophenol, 3,4–dimethyl–2–hydroxy–3–oxo–pentandioic acid, 2,4–dimethyl–2,3–dihydroxy–6–oxo–4–heptenoic acid, 2,4–dimethyl–4–hydroxy–2,3–epoxy– heptylic acid, 2,4–dimethyl–2,3,4–trihydroxy–5,6–dioxo–heptylic acid, and oligomer components were the predominant products in the aging particles. The possible reaction mechanisms leading to these aged products were also discussed and proposed.

Chemical composition of gas and particle-phase products of OH-initiated oxidation of 1,3,5-trimethylbenzene

Abstract A laboratory study was performed to investigate the composition of products formed from OH–initiated oxidation of aromatic hydrocarbon 1,3,5–trimethylbenzene. The experiments were conducted by irradiating 1,3,5–trimethylbenzene/CH 3 ONO/NO/air mixtures in smog chamber. The chemical composition of gas and particle–phase products have been investigated with gas chromatography/mass spectrometry (GC/MS) and the aerosol laser time–of–flight mass spectrometer (ALTOFMS), respectively. Experimental results showed that 3,5–dimethyl benzaldehyde, 2,4,6–trimethylphenol, 2–methyl–4–oxo–2–pentenal and 3,5–dimethyl–2–furanone were the predominant products in both the gas and particle–phases. However, there were some differences between detected gas–phase products and those of particle–phase, for example, oxalic acid, 2–methyl–2–hydroxy–3,4–dioxo–pentanal, and 2,3,5–trimethyl–3–nitro–phenol were only existing in the particle–phase. The possible reaction mechanisms leading to these products are also proposed. Compared to offline methods such as GC–MS measurement, the ALTOFMS detection can analyze real–time the secondary organic aerosol (SOA) successfully and provide more information on the products. Thus, ALTOFMS is a useful tool to reveal the formation and transformation processes of SOA particles in smog chambers.

Experimental and Theoretical Study of Reactions of OH Radicals with Hexenols: An Evaluation of the Relative Importance of the H-Abstraction Reaction Channel.

C6 hexenols are one of the most significant groups of volatile organic compounds with biogenic emissions. The lack of corresponding kinetic parameters and product information on their oxidation reactions will result in incomplete atmospheric chemical mechanisms and models. In this paper, experimental and theoretical studies are reported for the reactions of OH radicals with a series of C6 hexenols, (Z)-2-hexen-1-ol, (Z)-3-hexen-1-ol, (Z)-4-hexen-1-ol, (E)-2-hexen-1-ol, (E)-3-hexen-1-ol, and (E)-4-hexen-1-ol, at 298 K and 1.01 × 10(5) Pa. The corresponding rate constants were 8.53 ± 1.36, 10.1 ± 1.6, 7.86 ± 1.30, 8.08 ± 1.33, 9.10 ± 1.50, and 7.14 ± 1.20 (in units of 10(-11) cm(3) molecule(-1) s(-1)), respectively, measured by gas chromatography with a flame ionization detector (GC-FID), using a relative technique. Theoretical calculations concerning the OH-addition and H-abstraction reaction channels were also performed for these reactions to further understand the reaction mechanism and the relative importance of the H-abstraction reaction. By contrast to previously reported results, the H-abstraction channel is a non-negligible reaction channel for reactions of OH radicals with these hexenols. The rate constants of the H-abstraction channel are comparable with those for the OH-addition channel and contribute >20% for most of the studied alcohols, even >50% for (E)-3-hexen-1-ol. Thus, H-abstraction channels may have an important role in the reactions of these alcohols with OH radicals and must be considered in certain atmospheric chemical mechanisms and models.

Chemical analysis of aged benzene secondary organic aerosol using aerosol laser time-of-flight mass spectrometer

Secondary organic aerosol (SOA) from the photooxidation of aromatic compounds is a very complex mixture containing products with a different chemical nature that are dependent on aging processes. Aging of SOA particles formed from OH-initiated oxidation of benzene was investigated in a home-made smog chamber in this study. The chemical composition of aged benzene SOA particles were measured using aerosol laser time-of-flight mass spectrometer (ALTOFMS) coupled with Fuzzy C-Means (FCM) clustering algorithm. Experimental results showed that nitrophenol, dinitrophenol, nitrocatechol, dinitrocatechol, 6-oxo-2,4-hexadienoic acid, 2,4-hexadiendioic acid, 2,3-dihydroxy-6-oxo-4-hexenoic acid, 2,3-epoxy-4-hexendioic acid, 2,3-epoxy-4,5-dihydroxy-hexanedioic acid and high-molecular-weight (HMW) components were the predominant products in the aged particles. Compared to offline method such as liquid chromatography mass spectrometry (LC-MS) measurement, the real-time ALTOFMS detection approach coupled with the FCM data processing algorithm can make cluster analysis of SOA successfully and provide more information of products. The present results also indicate that benzene SOA aging proceeds through the oxidation of the internal double bond of ring-opened products, phenolic compounds, and acid-catalyzed heterogeneous reactions of carbonyl products. The possible reaction mechanisms leading to these aged products were also discussed and proposed.

A VUV photoionization mass spectrometric study on the OH-initiated photooxidation of isoprene with synchrotron radiation.

The gas-phase organic compounds resulting from OH-initiated photooxidation of isoprene have been investigated on-line by VUV photoionization mass spectrometry based on synchrotron radiation for the first time. The photoionization efficiency curves of the corresponding gaseous products as well as the chosen standards have been deduced by gating the interested peaks in the photoionization mass spectra while scanning the photon energy simultaneously, which permits the identification of the pivotal gaseous products of the photooxidation of isoprene, such as formaldehyde (10.84 eV), formic acid (11.38 eV), acetone (9.68 eV), glyoxal (9.84 eV), acetic acid (10.75 eV), methacrolein (9.91 eV), and methyl vinyl ketone (9.66 eV). Proposed reaction mechanisms leading to the formation of these key products were discussed, which were completely consistent with the previous works of different groups. The capability of synchrotron radiation photoionization mass spectrometry to directly identify the chemical composition of the gaseous products in a simulation chamber has been demonstrated, and its potential application in related studies of atmospheric oxidation of ambient volatile organic compounds is anticipated.

A Smog Chamber Facility for Qualitative and Quantitative Study on Atmospheric Chemistry and Secondary Organic Aerosol

In order to investigate the atmospheric oxidation processes and the formation of secondary organic aerosol (SOA), an indoor environmental reaction smog chamber are constructed and characterized. The system consists of the collapsible ∼830 L FEP Teflon film main reactor, in which the atmospheric chemical reactions take place and the formation of SOA occurs under the simulated atmospheric conditions, and the diverse on-line gas- and particle-phase instrumentation, such as the proton transfer reaction mass spectrometer, the synchrotron radiation photoionization mass spectrometer, the aerosol laser time-of-flight mass spectrometer, and other traditional commercial instruments. The initial characterization experiments are described, concerning the temperature and ultraviolet light intensity, the reactivity of the pure air, the wall loss rates of gaseous compounds and particulate matter. And the initial evaluation experiments for SOA yields from the ozonolysis of α-pinene and for mass spectra of the products re...

VUV photoionization aerosol mass spectrometric study on the iodine oxide particles formed from O3-initiated photooxidation of diiodomethane (CH2I2)

Iodine oxide particles (IOPs) formed from O3-initiated photooxidation of diiodomethane have been investigated based on the combination of a thermal desorption/tunable vacuum ultraviolet time-of-flight photoionization aerosol mass spectrometer (TD-VUV-TOF-PIAMS) with a flow reactor for the first time. Characterization of the home-made flow reactor was performed, which indicates the applicability of its combination with TD-VUV-TOF-PIAMS. Based on that, aerosol mass spectra of IOP formation from photooxidation of CH2I2/O3 were studied on-line taking full advantage of both the virtues of the flow reactor and TD-VUV-TOF-PIAMS. The main chemical components of IOPs, including atomic and molecular iodine (I, I2), iodine oxides (IO, OIO, I2O and I2O3) and hydrogen-containing iodine species (HI, HIO and HIO3), were observed and identified based on the corresponding photoionization energy (PIE) curves, and the probable chemical composition and formation mechanism of IOPs were proposed. The work has not only improved the understanding of the formation mechanism of IOPs, but also demonstrated the capability of TD-VUV-TOF-PIAMS for direct molecular characterization of aerosols in flow reactor experiments, whose potential application in mass spectrometric studies of atmospheric aerosols is anticipated.

Kinetics and mechanisms of gas phase reactions of hexenols with ozone

An absolute kinetic study is reported for the reactions of O3 with a series of C6 hexenols, (Z)-2-hexen-1-ol, (Z)-3-hexen-1-ol, (Z)-4-hexen-1-ol, (E)-2-hexen-1-ol, (E)-3-hexen-1-ol, and (E)-4-hexen-1-ol. At 298 K and atmospheric pressure, the rate constants (in units of 10−17 cm3 molecule−1 s−1) were measured to be 7.44 ± 1.03, 5.47 ± 0.71, 7.09 ± 0.91, 16.6 ± 2.2, 6.19 ± 0.72 and 10.5 ± 1.4, respectively. To gain a deeper insight into the reactivity and mechanism, theoretical calculations were also performed for the title reactions with the methods of density functional theory (DFT) and transition-state theory (TST). The geometries, energies, and harmonic vibrational frequencies of each stationary point were obtained at the BH&HLYP/6-31+G(d,p) level of theory. The calculated rate constants are in good agreement with the experimental data, and the reactivity of hexenols with O3 shows a strong dependence on their chemical structure based on the theoretical results. Finally, lifetimes of the C6 hexenols, with respect to their reactions with some important atmospheric oxidants such as O3, OH and NO3 radicals, have also been discussed in the article.