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Alternatively, the dissolved Br- ions tend to be substantially exhausted over a depth of 0-40 Å through the area because of charge repulsion from DS- ions within the interfacial region. These different interfacial Br- propensities correlate with formerly assessed gas-liquid reactivities gaseous Cl2 easily responds with Br- ions within the presence of THA+ but drops 70-fold into the existence of DS-, demonstrating that surfactant headgroup cost controls the reactiv
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