Pivalic acid as combined buffer and scavenger for studies of cloud water chemistry with pulse radiolysis
| Autor: | Thomas Nauser, Rolf E. Bühler |
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| Rok vydání: | 1994 |
| Předmět: | |
| Zdroj: | J. Chem. Soc., Faraday Trans.. 90:3651-3656 |
| ISSN: | 1364-5455 0956-5000 |
| DOI: | 10.1039/ft9949003651 |
| Popis: | The reactions of cloud water with transition-metal ions may be studies using pivalic acid as buffer and ˙OH scavenger. Commonly used phosphate buffers form strong complexes that may have an important effect on reaction kinetics. Low solubility products limit transition-metal ion concentrations to very low levels (micromolar). With pivalic acid as buffer, we can increase the CuII concentration typically by a factor of 340. At the same time better buffer characteristics and less complex formation is achieved. The scavenger efficiency equals that of tert-butyl alcohol.The rate data and the spectra of pivalic acid radicals have been measured in N2O-saturated solutions of pivalic acid. The acid constant was found to be 4.9 ± 0.1. The rate constants for the reaction of ˙OH with pivalic acid have been re-evaluated: k[(CH3)3CCO2–+˙OH]=(7 ± 2)× 108 dm3 mol–1 s–1 and k[(CH3)3CCO2H +˙OH]= 6.5 × 108 dm3 mol–1 s–1. The importance of including reactions like H˙+˙CH2(CH3)2CCO2H in the reaction model is shown. The rate constants for the recombination of pivalic acid radicals are: k[2˙CH2(CH3)2CCO2H]=(7 ± 1)× 108 dm3 mol–1 s–1, k[˙CH2(CH3)2CCO2H +˙CH2(CH3)2CCO2–]=(7 ± 3)× 108 dm3 mol–1 s–1 and k[2˙CH2(CH3)2CCO2–]=(3.7 ± 0.4)× 108 dm3 mol–1 s–1. |
| Databáze: | OpenAIRE |
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