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1.
Chemosphere ; 150: 329-340, 2016 May.
Artigo em Inglês | MEDLINE | ID: mdl-26921586

RESUMO

Singlet and triplet potential energy surfaces for the atmospheric ozonation of trans-2-chlorovnyldichloroarsine (lewisite) are investigated theoretically. Optimizations of the reactants, products, intermediates and transition states are carried out at the BHandHLYP/6-311+G(d,p) level. Single point energy calculations are performed at the CCSD(T)/6-311+G(d,p) level based on the optimized structures. The detailed mechanism is presented and discussed. Various possible H (or Cl)-abstraction and C (or As)-addition/elimination pathways are considered. The results show that the As-addition/elimination is more energetically favorable than the other mechanisms. Rice-Ramsperger-Kassel-Marcus (RRKM) theory is used to compute the rate constants over the possible atmospheric temperature range of 200-3000 K and the pressure range of 10(-8)-10(9) Torr. The calculated rate constant is in good agreement with the available experimental data. The total rate coefficient shows positive temperature dependence and pressure independence. The modified three-parameter Arrhenius expressions for the total rate coefficient and individual rate coefficients are represented. Calculation results show that major product is CHClCHAs(OOO)Cl2 (s-IM3) at the temperature below 600 K and O2 + CHClCHAsOCl2 (s-P9) play an important role at the temperature between 600 and 3000 K. Time-dependent DFT (TD-DFT) calculations indicate that CHCl(OOO)CHAsCl2 (s-IM3) and CHOAsCl2 (s-P5) can take photolysis easily in the sunlight. Due to the absence of spectral information for arsenide, computational vibrational spectra of the important intermediates and products are also analyzed to provide valuable evidence for subsequent experimental identification.


Assuntos
Poluentes Atmosféricos/análise , Arsenicais/análise , Substâncias para a Guerra Química/análise , Modelos Teóricos , Ozônio/química , Poluentes Atmosféricos/química , Poluentes Atmosféricos/efeitos da radiação , Arsenicais/química , Arsenicais/efeitos da radiação , Substâncias para a Guerra Química/química , Substâncias para a Guerra Química/efeitos da radiação , Cinética , Fotólise , Pressão , Temperatura Ambiente
2.
Appl Spectrosc ; 62(2): 238-47, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18284801

RESUMO

Several ionization potentials (IPs) of security relevant substances were determined with single photon ionization time of flight mass spectrometry (SPI-TOFMS) using monochromatized synchrotron radiation from the "Berliner Elektronenspeicherring-Gesellschaft für Synchrotronstrahlung" (BESSY). In detail, the IPs of nine explosives and related compounds, seven narcotics and narcotics precursors, and one chemical warfare agent (CWA) precursor were determined, whereas six IPs already known from the literature were verified correctly. From seven other substances, including one CWA precursor, the IP could not be determined as the molecule ion peak could not be detected. For these substances the appearance energy (AE) of a main fragment was determined. The analyzed security-relevant substances showed IPs significantly below the IPs of common matrix compounds such as nitrogen and oxygen. Therefore, it is possible to find photon energies in between, whereby the molecules of interest can be detected with SPI in very low concentrations due to the shielding of the matrix. All determined IPs except the one of the explosive EGDN were below 10.5 eV. Hence, laser-generated 118 nm photons can be applied for detecting almost all security-relevant substances by, e.g., SPI-TOFMS.


Assuntos
Substâncias para a Guerra Química/química , Substâncias Explosivas/química , Espectrometria de Massas/métodos , Fótons , Terrorismo/prevenção & controle , Substâncias para a Guerra Química/efeitos da radiação , Substâncias Explosivas/efeitos da radiação , Íons , Espectrometria de Massas/instrumentação , Síncrotrons
3.
J Hazard Mater ; 153(1-2): 37-43, 2008 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-17913350

RESUMO

Numerous methods are used for destruction of sulfur mustard. Oxidation is one of those methods. There have been only limited data concerning application of the advanced oxidation technologies (AOTs) for mustard destruction available before. In this study sulfur mustard oxidation rate depending on kind of the oxidative system and process parameters used was assessed using selected AOT. The following were selected for mustard oxidation: ozone (O(3)), UV light (UV), hydrogen peroxide (H(2)O(2)); double systems: UV/O(3), UV/H(2)O(2), and O(3)/H(2)O(2); a triple system: O(3)/H(2)O(2)/UV and Fenton reaction. Effectiveness of the selected AOT methods has been evaluated and the most suitable one for mustard destruction was chosen. Using ozone in various combinations with hydrogen peroxide and UV radiation mustard can be destroyed much quicker comparing to the classical oxidizers. Fast mustard oxidation (a few minutes) occurred in those systems where ozone alone was used, or in the following combinations: O(3)/H(2)O(2), O(3)/UV and O(3)/H(2)O(2)/UV. When those advanced oxidation technologies are used, mustard becomes destroyed mainly in course of the direct oxidation with ozone, and reactions of mustard with radicals formed due to ozone action play a secondary role. Rate of sulfur mustard oxidation in the above mentioned ozone-containing oxidative systems decreases with pH value increasing from 2 to 12. Only when pH value of reaction solutions is close to pH 5, mustard oxidation rate is minimal, probably due to "disappearance" of radicals participating in oxidation in this pH. Sulfur mustard can be most effectively destroyed using just ozone in pH 7. In that case mustard destruction rate is only slightly lower than the rate achieved in optimal conditions, and the system is the simplest.


Assuntos
Substâncias para a Guerra Química , Peróxido de Hidrogênio/química , Gás de Mostarda , Oxidantes/química , Ozônio/química , Raios Ultravioleta , Substâncias para a Guerra Química/química , Substâncias para a Guerra Química/efeitos da radiação , Concentração de Íons de Hidrogênio , Gás de Mostarda/química , Gás de Mostarda/efeitos da radiação , Oxirredução
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