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Table 3 Standard Gibbs free energies (∆G0′) of different degradation reactions of phenylacetate (C8H7O2−) and phenylpropionate (C9H9O2−)

From: Formation of phenylacetic acid and phenylpropionic acid under different overload conditions during mesophilic and thermophilic anaerobic digestion

No

Reactiona

∆G0′ [kJ mol−1 substrate]

 

1

C8H7O2− + 8 H2O → 3 CH3COO− + 2 CO2 + 6 H2 + 2 H+

+ 123.1

Phenylacetate conversion to acetate, CO2 and H2 via α-oxidation

2

C9H9O2− + 2 H2O → C8H7O2− + CO2 + 3 H2

+ 73.6

Phenylpropionate conversion to phenylacetate, CO2 and H2 via α-oxidation

3

C9H9O2− + 10 H2O → 3 CH3COO− + 3 CO2 + 9 H2 + 2 H+

+ 196.7

Phenylpropionate conversion to acetate, CO2 and H2 via α-oxidation

  1. aReactions according to [19]