Articles | Volume 11, issue 5
https://doi.org/10.5194/amt-11-3081-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
https://doi.org/10.5194/amt-11-3081-2018
© Author(s) 2018. This work is distributed under
the Creative Commons Attribution 4.0 License.
the Creative Commons Attribution 4.0 License.
Identification of organic hydroperoxides and peroxy acids using atmospheric pressure chemical ionization–tandem mass spectrometry (APCI-MS/MS): application to secondary organic aerosol
Department of Chemistry, University of Toronto, Toronto, Canada
Jean C. Rivera-Rios
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
Frank N. Keutsch
Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA
School of Engineering and Applied Sciences, Harvard University, Cambridge, MA, USA
Jonathan P. D. Abbatt
Department of Chemistry, University of Toronto, Toronto, Canada
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46 citations as recorded by crossref.
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- Formation of extremely low-volatility organic compounds from styrene ozonolysis: Implication for nucleation S. Yu et al. 10.1016/j.chemosphere.2022.135459
- Reaction of Condensed-Phase Criegee Intermediates with Carboxylic Acids and Perfluoroalkyl Carboxylic Acids S. Zhou et al. 10.1021/acs.estlett.9b00165
- Gas phase H+, H3O+ and NH4+ affinities of oxygen-bearing volatile organic compounds; DFT calculations for soft chemical ionisation mass spectrometry M. Omezzine Gnioua et al. 10.1039/D3CP03604A
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- NH4+ Association and Proton Transfer Reactions With a Series of Organic Molecules E. Canaval et al. 10.3389/fchem.2019.00191
- Aqueous-phase fates of α-alkoxyalkyl-hydroperoxides derived from the reactions of Criegee intermediates with alcohols M. Hu et al. 10.1039/D0CP06308H
- Interfacial vs Bulk Ozonolysis of Nerolidol J. Qiu et al. 10.1021/acs.est.9b00364
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- Accounting for Cloud Nucleation Activation Mechanism of Secondary Organic Matter from α-Pinene Oxidation Using Experimentally Retrieved Water Solubility Distributions W. Lee et al. 10.1021/acs.est.3c03039
- Organic Peroxides and Sulfur Dioxide in Aerosol: Source of Particulate Sulfate S. Wang et al. 10.1021/acs.est.9b02591
- Exploring hydroperoxides in combustion: History, recent advances and perspectives Z. Wang et al. 10.1016/j.pecs.2019.02.003
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- Accurate identification of dimers from α‐pinene oxidation using high‐resolution collision‐induced dissociation mass spectrometry K. Sekimoto et al. 10.1002/jms.4508
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46 citations as recorded by crossref.
- Analytical methodologies for oxidized organic compounds in the atmosphere A. Tiusanen et al. 10.1039/D3EM00163F
- Evidence for sustainably reducing secondary pollutants in a typical industrial city in China: Co-benefit from controlling sources with high reduction potential beyond industrial process Y. Niu et al. 10.1016/j.jhazmat.2024.135556
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- Isomer-Resolved Reactivity of Organic Peroxides in Monoterpene-Derived Secondary Organic Aerosol M. Yao et al. 10.1021/acs.est.2c01297
- Application of time-of-flight aerosol mass spectrometry for the real-time measurement of particle-phase organic peroxides: an online redox derivatization–aerosol mass spectrometer (ORD-AMS) M. Weloe & T. Hoffmann 10.5194/amt-13-5725-2020
- Synthesis and characterisation of peroxypinic acids as proxies for highly oxygenated molecules (HOMs) in secondary organic aerosol S. Steimer et al. 10.5194/acp-18-10973-2018
- Formation of extremely low-volatility organic compounds from styrene ozonolysis: Implication for nucleation S. Yu et al. 10.1016/j.chemosphere.2022.135459
- Reaction of Condensed-Phase Criegee Intermediates with Carboxylic Acids and Perfluoroalkyl Carboxylic Acids S. Zhou et al. 10.1021/acs.estlett.9b00165
- Gas phase H+, H3O+ and NH4+ affinities of oxygen-bearing volatile organic compounds; DFT calculations for soft chemical ionisation mass spectrometry M. Omezzine Gnioua et al. 10.1039/D3CP03604A
- Autoxidation of glycols used in inhalable daily products: implications for the use of artificial fogs and e-cigarettes X. Guo et al. 10.1039/D3EM00214D
- NH4+ Association and Proton Transfer Reactions With a Series of Organic Molecules E. Canaval et al. 10.3389/fchem.2019.00191
- Aqueous-phase fates of α-alkoxyalkyl-hydroperoxides derived from the reactions of Criegee intermediates with alcohols M. Hu et al. 10.1039/D0CP06308H
- Interfacial vs Bulk Ozonolysis of Nerolidol J. Qiu et al. 10.1021/acs.est.9b00364
- Synthesis and Characterization of Atmospherically Relevant Hydroxy Hydroperoxides P. Mettke et al. 10.3390/atmos13040507
- Fates of Organic Hydroperoxides in Atmospheric Condensed Phases S. Enami 10.1021/acs.jpca.1c01513
- Photooxidation-Initiated Aqueous-Phase Formation of Organic Peroxides: Delving into Formation Mechanisms T. Gautam et al. 10.1021/acs.est.3c01162
- Water Dramatically Accelerates the Decomposition of α-Hydroxyalkyl-Hydroperoxides in Aerosol Particles J. Qiu et al. 10.1021/acs.jpclett.9b01953
- Diverse Reactions in Highly Functionalized Organic Aerosols during Thermal Desorption Z. Zhao et al. 10.1021/acsearthspacechem.9b00312
- Indoor Illumination of Terpenes and Bleach Emissions Leads to Particle Formation and Growth C. Wang et al. 10.1021/acs.est.9b04261
- Stability of Monoterpene-Derived α-Hydroxyalkyl-Hydroperoxides in Aqueous Organic Media: Relevance to the Fate of Hydroperoxides in Aerosol Particle Phases J. Qiu et al. 10.1021/acs.est.9b07497
- Decomposition of multifunctionalized α-alkoxyalkyl-hydroperoxides derived from the reactions of Criegee intermediates with diols in liquid phases Y. Endo et al. 10.1039/D2CP00915C
- Heterogeneous Ozonolysis of Endocyclic Unsaturated Organic Aerosol Proxies: Implications for Criegee Intermediate Dynamics and Later-Generation Reactions Z. Zhao et al. 10.1021/acsearthspacechem.8b00177
- Dark air–liquid interfacial chemistry of glyoxal and hydrogen peroxide F. Zhang et al. 10.1038/s41612-019-0085-5
- Molecular composition of secondary organic aerosol from styrene under different NO and humidity conditions S. Yu et al. 10.1016/j.atmosres.2021.105950
- Chemical Fate of Oils on Indoor Surfaces: Ozonolysis and Peroxidation Z. Zhou et al. 10.1021/acs.est.3c04009
- Peroxides on the Surface of Organic Aerosol Particles Using Matrix-Assisted Ionization in Vacuum (MAIV) Mass Spectrometry Y. Qin et al. 10.1021/acs.est.3c02895
- Eudesmane and Eremophilane Sesquiterpenes from the Fruits of Alpinia oxyphylla with Protective Effects against Oxidative Stress in Adipose-Derived Mesenchymal Stem Cells P. Thapa et al. 10.3390/molecules26061762
- Toxicological Responses of α-Pinene-Derived Secondary Organic Aerosol and Its Molecular Tracers in Human Lung Cell Lines F. Khan et al. 10.1021/acs.chemrestox.0c00409
- Atmospheric Chemistry Analysis: A Review P. Forbes 10.1021/acs.analchem.9b04623
- Temperature Dependence of Aqueous-Phase Decomposition of α-Hydroxyalkyl-Hydroperoxides M. Hu et al. 10.1021/acs.jpca.0c09862
- Reactivity of Monoterpene Criegee Intermediates at Gas–Liquid Interfaces J. Qiu et al. 10.1021/acs.jpca.8b06914
- Copper Hexacyanoferrate as a Novel Electrode Material in Electrochemical Detection of Cumene Hydroperoxide C. Moonla et al. 10.1149/1945-7111/ac3780
- Analytical methods for peroxo acids – a review F. Sode 10.1039/C9AY00860H
- Modelling ultrafine particle growth in a flow tube reactor M. Taylor Jr. et al. 10.5194/amt-15-4663-2022
- The role of functional groups in the understanding of secondary organic aerosol formation mechanism from α-pinene L. Jia & Y. Xu 10.1016/j.scitotenv.2020.139831
- Proton-Catalyzed Decomposition of α-Hydroxyalkyl-Hydroperoxides in Water J. Qiu et al. 10.1021/acs.est.0c03438
- Accounting for Cloud Nucleation Activation Mechanism of Secondary Organic Matter from α-Pinene Oxidation Using Experimentally Retrieved Water Solubility Distributions W. Lee et al. 10.1021/acs.est.3c03039
- Organic Peroxides and Sulfur Dioxide in Aerosol: Source of Particulate Sulfate S. Wang et al. 10.1021/acs.est.9b02591
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- Organic Peroxides in Aerosol: Key Reactive Intermediates for Multiphase Processes in the Atmosphere S. Wang et al. 10.1021/acs.chemrev.2c00430
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- Accurate identification of dimers from α‐pinene oxidation using high‐resolution collision‐induced dissociation mass spectrometry K. Sekimoto et al. 10.1002/jms.4508
- Potential Matrix Effects in Iodometry Determination of Peroxides Induced by Olefins T. Gautam et al. 10.1021/acs.jpca.1c10717
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- Simultaneous Quantification of H2O2 and Organic Hydroperoxides by 1H NMR Spectroscopy T. Kakeshpour & A. Bax 10.1021/acs.analchem.2c00264
Latest update: 22 Nov 2024