Corrosion of reinforcing steel is a major cause for degradation of concrete structures,especially when exposed to chloride ions.Thus,the Silver/Nano-silver Chloride (SNSC) electrodes as sensors of chloride concentrati...Corrosion of reinforcing steel is a major cause for degradation of concrete structures,especially when exposed to chloride ions.Thus,the Silver/Nano-silver Chloride (SNSC) electrodes as sensors of chloride concentration were prepared and encapsulated carefully.The properties of the electrode were studied by emerging them in a series of concrete pore solutions with different admixed KCl contents.These SNSC sensors show that good stability in concrete pore solutions at room temperature.Polarization disposal can shorten the stabilized period of the sensors.The electrochemical tests indicate the SNSC sensors with desirable linearity and reproducibility.The response time of SNSC sensors is short enough for monitoring the chloride ions concentration in concrete structures.The good performance of SNSC sensors indicate that they could be embedded in the concrete structures in the future.展开更多
The effects of cerium nitrite on corrosion behaviors of carbon steel in simulated concrete pore solutions were studied with the methods of linear polarization, electrochemical impedance spectroscopy and surface analys...The effects of cerium nitrite on corrosion behaviors of carbon steel in simulated concrete pore solutions were studied with the methods of linear polarization, electrochemical impedance spectroscopy and surface analysis. In pore solutions in the presence of Ce（NO3）3？6H2O, the corrosion potential, polarization resistance and impedance of carbon steel obviously increased in contrast to the situation in the absence of cerium salts. The pore solution with [NO2-] / [Cl-] = 0.3 and 0.1% Ce（NO3）3？6H2O, carbon steel shows better corrosion resistance than that in the pore solution with [NO2-] / [Cl-] = 0.6, which indicates that a small amount of Ce（NO3）3？6H2O in pore solutions can effectively promote passivation of the steel and reduce the threshold [NO2-] / [Cl-] ratio for corrosion control. The surface layer formed in cerium salt containing pore solutions is more compact and smooth and 1.36%Ce is examined on the sample surface. The addition of 0.1% Ce（NO3）3？6H2O in pore solutions can decrease the corrosion rate of steel in pore solutions and has little influence on pH change of the solutions. However, more cerium nitrate addition above 0.1% may result in pH decrease of the solution.展开更多
The electrochemical behavior of metallic passive film on rebar in concrete is characterized by its semiconductive nature. The charge distribution at the interface between a semiconductor and an electrolyte is often de...The electrochemical behavior of metallic passive film on rebar in concrete is characterized by its semiconductive nature. The charge distribution at the interface between a semiconductor and an electrolyte is often determined by measuring the capacitance of the space-charge layer （Csc） as a function of the electrode potential （E）. When the space charge-layer serves as the depletion layer, the relation of Csc^-2 vs E resembles a Mott-Schottky plot （M-S plot）. The semiconductive properties of the passive film on rebar in concrete were analyzed with M-S plots to study the effect of chloride ions and mineral admixtures on rebar passive films. Some rebar electrodes were immersed in simulated concrete pore solutions, while others were embedded in concrete with/without mineral admixtures. In saturated Ca（OH）, solutions, the relation of Csc^-2-E of rebar electrodes shows linear MottSchottky relationship indicating that the passive film on rebar is a highly disordered n-type semiconductor, with donor density （ND） in the order of 10^26m^-3. After adding chloride ions （Cl wt%〈0.2%） in system solutions, the M-S plot slopes significantly decreased and ND increased, suggesting that chloride ion will cause passive film corrosion and breakdown. The M-S plots of the passive film on rebar electrodes embedded in concrete were similar to those immersed in simulated system solution. However, ND of those in concrete with mineral admixtures tended to be a little smaller, indicating that introducing proper quantity admixtures into concrete could make the rebar passive film have a thicker space-charge layer and therefore a thicker passive film layer.展开更多
基金Funded by the National Natural Science Foundation of China (No.50678053)
文摘Corrosion of reinforcing steel is a major cause for degradation of concrete structures,especially when exposed to chloride ions.Thus,the Silver/Nano-silver Chloride (SNSC) electrodes as sensors of chloride concentration were prepared and encapsulated carefully.The properties of the electrode were studied by emerging them in a series of concrete pore solutions with different admixed KCl contents.These SNSC sensors show that good stability in concrete pore solutions at room temperature.Polarization disposal can shorten the stabilized period of the sensors.The electrochemical tests indicate the SNSC sensors with desirable linearity and reproducibility.The response time of SNSC sensors is short enough for monitoring the chloride ions concentration in concrete structures.The good performance of SNSC sensors indicate that they could be embedded in the concrete structures in the future.
基金the National Natural Science Foundation of China(No.50731004)Technology Support Programs of China(No.2007BAB27B04-N43CTT)
文摘The effects of cerium nitrite on corrosion behaviors of carbon steel in simulated concrete pore solutions were studied with the methods of linear polarization, electrochemical impedance spectroscopy and surface analysis. In pore solutions in the presence of Ce（NO3）3？6H2O, the corrosion potential, polarization resistance and impedance of carbon steel obviously increased in contrast to the situation in the absence of cerium salts. The pore solution with [NO2-] / [Cl-] = 0.3 and 0.1% Ce（NO3）3？6H2O, carbon steel shows better corrosion resistance than that in the pore solution with [NO2-] / [Cl-] = 0.6, which indicates that a small amount of Ce（NO3）3？6H2O in pore solutions can effectively promote passivation of the steel and reduce the threshold [NO2-] / [Cl-] ratio for corrosion control. The surface layer formed in cerium salt containing pore solutions is more compact and smooth and 1.36%Ce is examined on the sample surface. The addition of 0.1% Ce（NO3）3？6H2O in pore solutions can decrease the corrosion rate of steel in pore solutions and has little influence on pH change of the solutions. However, more cerium nitrate addition above 0.1% may result in pH decrease of the solution.
基金Project (No. 502019) supported by the Natural Science Foundationof Zhejiang Province, China
文摘The electrochemical behavior of metallic passive film on rebar in concrete is characterized by its semiconductive nature. The charge distribution at the interface between a semiconductor and an electrolyte is often determined by measuring the capacitance of the space-charge layer （Csc） as a function of the electrode potential （E）. When the space charge-layer serves as the depletion layer, the relation of Csc^-2 vs E resembles a Mott-Schottky plot （M-S plot）. The semiconductive properties of the passive film on rebar in concrete were analyzed with M-S plots to study the effect of chloride ions and mineral admixtures on rebar passive films. Some rebar electrodes were immersed in simulated concrete pore solutions, while others were embedded in concrete with/without mineral admixtures. In saturated Ca（OH）, solutions, the relation of Csc^-2-E of rebar electrodes shows linear MottSchottky relationship indicating that the passive film on rebar is a highly disordered n-type semiconductor, with donor density （ND） in the order of 10^26m^-3. After adding chloride ions （Cl wt%〈0.2%） in system solutions, the M-S plot slopes significantly decreased and ND increased, suggesting that chloride ion will cause passive film corrosion and breakdown. The M-S plots of the passive film on rebar electrodes embedded in concrete were similar to those immersed in simulated system solution. However, ND of those in concrete with mineral admixtures tended to be a little smaller, indicating that introducing proper quantity admixtures into concrete could make the rebar passive film have a thicker space-charge layer and therefore a thicker passive film layer.
