2007
DOI: 10.1002/cite.200600113
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Epoxidierung von C=C‐Doppelbindungen mit in situ erzeugtem Wasserstoffperoxid

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Cited by 1 publication
(2 citation statements)
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“…An industrial process (the anthraquinone process) for the synthesis of hydrogen peroxide involves reacting hydroquinone with molecular oxygen [Figure ] at temperatures around 30–80 °C and a pressure of 5 bar, comparable with the conditions employed in these experiments. The resulting hydrogen peroxide can serve as an oxidizing agent for the components of the model fuels . It was shown that quinones are formed in a model fuel, stressed for 5 h at 160 °C under a constant airflow of 100 mL/min …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…An industrial process (the anthraquinone process) for the synthesis of hydrogen peroxide involves reacting hydroquinone with molecular oxygen [Figure ] at temperatures around 30–80 °C and a pressure of 5 bar, comparable with the conditions employed in these experiments. The resulting hydrogen peroxide can serve as an oxidizing agent for the components of the model fuels . It was shown that quinones are formed in a model fuel, stressed for 5 h at 160 °C under a constant airflow of 100 mL/min …”
Section: Resultsmentioning
confidence: 99%
“…The resulting hydrogen peroxide can serve as an oxidizing agent for the components of the model fuels. 19 It was shown that quinones are formed in a model fuel, stressed for 5 h at 160 °C under a constant airflow of 100 mL/min. 20 2-Phenylphenol causes a slight rise in the induction time but, compared with 2-methylphenol, this effect is weaker.…”
Section: Resultsmentioning
confidence: 99%