Quantitative Detection of Corrosion State of Concrete Internal Reinforcement Based on Metal Magnetic Memory

Corrosion can be very harmful to the service life and several properties of reinforced concrete structures.The metal magnetic memory(MMM)method,as a newly developed spontaneous magnetic flux leakage(SMFL)non-destructive testing(NDT)technique,is considered a potentially viable method for detecting corrosion damage in reinforced concrete members.To this end,in this paper,the indoor electrochemical method was employed to accelerate the corrosion of outsourced concrete specimens with different steel bar diameters,and the normal components Bz and its gradient of the SMFL fields on the specimen surfaces were investigated based on the metal magnetic memory(MMM)method.The experimental results showed that the SMFL experimental Bz curves are consistent with the analytical results of the theoretical model.Furthermore,the crest-to-trough behavior on the Bz signal curve and its zero-point gradient spacing can more accurately indicate the corroded area’s extent.Then,a magnetic characteristic parameter W based on a large amount of experimental data was established to characterize the degree of corrosion of the steel bars.The magnetic characteristic parameter W is linearly related to the maximum cross-sectional area loss rate
of the corroded reinforcement.This paper will lay the foundation for future research on corrosion detection of reinforced concrete structures based on the MMM method and provide a feasible way for non-destructive detection of corrosion independent of the influence of reinforcement diameter and magnetization history.

Effect of specifically-adsorbed polysulfides on the electron transfer kinetics of sodium metal anodes

Room-temperature sodium-sulfur(RT Na-S)batteries hold great promise for large-scale energy storage applications owing to the high energy density and earth-abundance of Na and S.However,the dissolution and migration of sodium polysulfides,uncontrollable Na dendrite growth,and the lack of studies on Na electrodeposition kinetics have hindered the development of these batteries.Herein,we reveal the mechanism of sodium polysulfides on the Na plating/stripping kinetics using a three-electrode system.First,the kinetic behavior deviates from the commonly supposed Butler-Volmer model,which is well described by the Marcus model.In addition,the specific adsorption of polysulfides on the sodium electrode surface is a key factor influencing the kinetics.Higher-order polysulfides(S_(8)^(2-)and S_(6)^(2-))exhibit distinct specific adsorption behaviors because of their high adsorption energies compared to lower-order polysulfides(S_(4)^(2-)and S_(2)^(2-)).The electrostatic effect caused by specific adsorption can accelerate the kinetics,whereas the blocking effect can slow the kinetics.Thus,this competitive relationship enables low concentrations of high-order polysulfides to stimulate kinetics.This implies that a weak shuttle effect is beneficial for obtaining a stable Na deposition in RT Na-S batteries.An in-depth understanding of the Na electrodeposition kinetics provides beneficial clues for future metal sodium/electrolyte interface designs.