Henglein A, Kormann C
Int J Radiat Biol Relat Stud Phys Chem Med. 1985 Aug;48(2):251-8. doi: 10.1080/09553008514551241.
The yield of hydrogen peroxide in the sonication of argon-saturated water was studied in the presence of various solutes. The efficiency of OH radical scavenging is expressed by the reciprocal value of C 1/2, the solute concentration at which the H2O2 yield is decreased by 50 per cent. C 1/2 ranges over several orders of magnitude. It is not related to the specific reactivity towards OH in homogeneous solution. However, it is correlated to the hydrophobicity of the solutes. The competition of I- and a second solute for OH was also studied. The competition between I- and HCO2- follows similar kinetics as in homogeneous solution. However, many other solutes compete in the manner which would be expected if radical scavenging occurred in different phases. The effects are explained in terms of OH radical formation in gaseous argon bubbles, combination of OH radicals to form H2O2 in an interfacial area, and enrichment of hydrophobic solutes in the bubbles.
在各种溶质存在的情况下,研究了氩饱和水超声处理过程中过氧化氢的产率。羟基自由基清除效率用C 1/2的倒数表示,C 1/2是使过氧化氢产率降低50%时的溶质浓度。C 1/2的范围跨越几个数量级。它与在均相溶液中对羟基的特定反应性无关。然而,它与溶质的疏水性相关。还研究了碘离子与第二种溶质对羟基的竞争。碘离子与甲酸根离子之间的竞争遵循与均相溶液中相似的动力学。然而,许多其他溶质的竞争方式符合自由基清除在不同相发生时的预期情况。这些效应可以通过气态氩气泡中羟基自由基的形成、羟基自由基在界面区域结合形成过氧化氢以及气泡中疏水性溶质的富集来解释。