Related Experiment Video
Updated: Aug 6, 2026

A Method to Test the Efficacy of Handwashing for the Removal of Emerging Infectious Pathogens
Published on: June 7, 2017
Comparison of virucidal activity between weakly acidified chlorous acid water and sodium hypochlorite solution
Keiko Ikeda1, Isanori Horiuchi2, Hisataka Goda2
1School of Health and Nursing Science, Wakayama Medical University, Wakayama 641-0011, Japan.
Abstract:
The virucidal activities of weakly acidified chlorous acid water (WACAW) were characterized in comparison to those of sodium hypochlorite solution (NaClO), using polioviruses type 1 and 3 (PV-1 and PV-3). In the absence of interfering substances, more than 10-4 reduction of the infectivity was achieved by NaClO at 5 p.p.m. and by WACAW at 0.75 p.p.m. of free available chlorine (FAC) concentration. Similarly, in the presence of 0.5% polypepton, more than four logs (99.99% or more) reduction of infectious virus for PV-1 and PV-3 was achieved by the incubation with NaClO at 2,000 p.p.m. but not at 500 p.p.m., while it was achieved by the incubation with WACAW at 100 p.p.m. but not at 50 p.p.m. These results show that WACAW was more effective than NaClO at the same FAC concentrations regardless of the presence of interfering substances, suggesting a general advantage of the WACAW for practical applications as a disinfectant.
Related Concept Videos
Weak Acid Solutions
Mixtures of Acids
A Mixture of a Strong Acid and a Weak Acid
In a mixture of a strong acid and a weak acid, the strong acid dissociates completely and becomes a source of almost all the hydronium ions...
Mixtures of Acids
In a strong and weak acid mixture, the strong acid dissociates completely and becomes a source of almost all the hydronium ions present in the solution. In contrast, the weak acid shows...
Leveling Effect and Non-Aqueous Acid-Base Solutions
The Leveling Effect of a Solvent
A generic acid (HA) reacts with the generic base (B-) to yield the corresponding conjugate base (A-) and conjugate acid (HB):
Polyprotic Acids
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
