Peroxynitrates (RO2NO2), in particular acyl peroxynitrates (R = R′C(O) with R′ = alkyl), are prominent constituents of polluted air. In this work, a systematic study on the thermal decomposition rate constants of the first five members of the series of homologous R′C(O)O2NO2 with R′ = CH3 ( =PAN), C2H5, n‐C3H7, n‐C4H9, and n‐C5H11 is undertaken to verify the conclusions from previous laboratory data (Grosjean et al., Environ. Sci. Technol. 1994, 28, 1099–1105; Grosjean et al., Environ. Sci. Technol. 1996, 30, 1038–1047; Bossmeyer et al., Geophys. Res. Lett. 2006, 33, L18810) that the longer chain peroxynitrates may be considerably more stable than PAN. Experiments are performed in a temperature‐controlled, evacuable 200 L‐photoreactor made from quartz. n‐Acyl peroxynitrates are generated by stationary photolysis of mixtures of molecular bromine, O2, NO2, and the corresponding parent aldehydes, highly diluted in N2. Thermal decomposition of R′C(O)O2NO2 is initiated by the addition of an excess of NO. First‐order decomposition rate constants k1 of the reactions R′C(O)O2NO2 (+M) → R′C(O)O2 + NO2 (+M) are derived at 298 K and a total pressure of 1 bar from the measured loss rates of R′C(O)O2NO2, correcting for wall loss of R′C(O)O2NO2 and several percentages of reformation of R′C(O)O2NO2 by the reaction of R′C(O)O2 radicals with NO2. With increasing chain length of R′, k1(298 K) slightly decreases from 4.4 × 10−4 s−1 (R′ = CH3) to 3.7 × 10−4 s−1 (R′ = C2H5), leveling off at (3.4 ± 0.1) × 10−4 s−1 for R′ = n‐C3H7, n‐C4H9, and n‐C5H11. Temperature dependencies of k1 were measured for CH3C(O)O2NO2 and n‐C5H11C(O)O2NO2 in the temperature range 289–308 K, resulting in the same activation energy within the statistical error limits (2σ) of 0.9 and 1.5 kJ mol−1, respectively. A few experiments on n‐C6H13C(O)O2NO2, n‐C7H15C(O)O2NO2, and n‐C8H17C(O)O2NO2 were also performed, but the results were considered to be unreliable due to strong wall loss of the peroxynitrate and possible complications caused by radical‐sinitiated side reactions.

No abstract

No abstract

No abstract

A feasible catalytic reactor for oxygen evolution has been proposed, which could complement the current methods of O2 evolution efficiently and ensure the availability of pure oxygen on a wider scale. Several chemicals, such as NaI, MnO2, NiSO4, etc. can generally decompose hydrogen peroxide by producing oxygen as a product via chemical reactions. Meanwhile, the Pt-Pd catalyst efficiently catalyzes hydrogen peroxide decomposition reactions and generates pure oxygen without any unfriendly species. The excellence of the bi-metallic catalyst has been validated by the evaluation of turnover number (TON) and turnover frequency (TOF). Implementing the knowledge of chemical reactions and heterogenous catalysis, the proposed catalytic reactor could be helpful for generating a continuous flow of oxygen. Surely, the oxygen produced in this process is higher in amount compared to the oxygen present in the atmosphere at ambient conditions which might facilitate the breathing support for critically ill patients.