scholarly journals Effect of Electrical Injection of Corrosion Inhibitor on the Corrosion of Steel Rebar in Chloride-Contaminated Repair Mortar

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
The Huyen Nguyen ◽  
Tuan Anh Nguyen ◽  
Thien Vuong Nguyen ◽  
Van Khu Le ◽  
Thi Mai Thanh Dinh ◽  
...  

The electrical rehabilitation treatments of repair mortar were performed with tetrabutylammonium bromide salt (TBAB) at an electrical current density of 5 A/m2, using two electrolytes (0.1 M NaOH and 0.1 M Na3BO3solutions), and for two time periods (1 and 4 weeks), respectively. The average organic cation-based inhibitor’s concentration in cement mortars before and after this treatment was quantified using the UV-Vis spectroscopy. The experimental results reveal that the EICI treatment with 0.1 M Na3BO3was more effective in injecting the inhibitor and in improving the chloride penetration resistance and compressive strength of the mortar, relative to using 0.1 M NaOH as electrolyte. In this case, after the 4-week EICI treatment, [TBA+] contents were 2.3 % and 2.4% by mass of cement mortar for uncontaminated and salt-contaminated mortars, respectively. After the 4-week EICI treatment, the apparent diffusion coefficients of chloride anion in cement mortar were decreased by 40% from 1.52 × 10−10 m2/s. The EICI treatment was able to halt the chloride-induced corrosion of the steel rebar by promoting its passivation. The 2-week EICI treatment using sodium hydroxide and sodium borate solutions decreased the corrosion current density of the rebar by 77.8% and 78.5%, respectively, approximately two months after the treatment.

CORROSION ◽  
2012 ◽  
Vol 68 (4) ◽  
pp. 045003-1-045003-10 ◽  
Author(s):  
M. Akhoondan ◽  
A.A. Sagüés

The extent of the oxygen reduction reaction in concrete was evaluated for ~9% Cr rebar approaching the ASTM A1035 specification and compared to that of conventional carbon steel rebar, at ages of up to ~1 year. Cathodic strength was measured by the cathodic current density developed at −0.35 V vs. copper/copper sulfate (Cu/CuSO4 [CSE]) and −0.40 VCSE in cyclic cathodic potentiodynamic polarization tests, both in the as-received condition with mill scale and with scale removed by glass bead surface blasting. In both conditions the ~9% Cr alloy was a substantially weaker cathode, by a factor of several fold, than carbon steel. Within each material, the surface-blasted condition yielded also much lower cathodic current density than the as-received condition. For a small anode-large cathode system with a given anode polarization function, and no important oxygen reduction concentration polarization, the corrosion current was projected to be significantly lower if the cathodic region were ~9% Cr instead of plain steel rebar with comparable surface condition. There was strong correlation between the charge storage capability of the interface and the extent of cathodic reaction of oxygen. The result cannot be ascribed solely to differences in effective surface area between the different materials and conditions.


2015 ◽  
Vol 2015 ◽  
pp. 1-15 ◽  
Author(s):  
Zhonglu Cao ◽  
Makoto Hibino ◽  
Hiroki Goda

The effect of nitrite ions on the macrocell corrosion behavior of reinforcing steel embedded in cement mortar was investigated by comparing and analyzing the macrocell corrosion current, macrocell polarization ratios, and slopes of anodic and cathodic steels. Based on the experimental results, the relationship between macrocell potential difference and macrocell current density was analyzed, and the mechanism of macrocell corrosion affected by nitrite ions was proposed. The results indicated that nitrite ions had significant impact on the macrocell polarization ratios of cathode and anode. The presence of nitrite could reduce the macrocell current by decreasing the macrocell potential difference and increasing the macrocell polarization resistance of the anode.


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
The Huu Nguyen ◽  
Tuan Anh Nguyen

Epoxy reinforced with two kinds of nanoparticles dealing with nano-SiO2 and nano-Fe2O3 was coated on steel rebar embedded in a chloride contaminated cement mortar. NaCl was added to the fresh Portland cement paste (at 0.3% and 0.5% by weight of cement) to simulate the chloride contamination at the critical level. The effect of incorporating nanoparticles on the corrosion resistance of epoxy-coated steel rebar was investigated by linear potentiodynamic polarization and electrochemical impedance spectroscopy. For the 0.3 wt.% chloride mortars, the electrochemical monitoring of the coated steel rebars during immersion for 56 days in 0.1 M NaOH solutions suggested the beneficial role of nano-Fe2O3 particles in significantly improving the corrosion resistance of the epoxy-coated rebar. After 56 days of immersion, the nano-Fe2O3 reduced the corrosion current of epoxy-coated rebar by a factor of 7.9. When the chloride concentration in the cement mortar was 0.5 wt.%, the incorporation of nanoparticles into the epoxy matrix did not enhance the corrosion resistance of epoxy coating for the rebar. At this critical level, chloride ions initiated rebar corrosion through nanoparticles at the epoxy/rebar interface.


2020 ◽  
Vol 9 (1) ◽  
pp. 496-502 ◽  
Author(s):  
Zhaohui Zhang ◽  
Bailong Liu ◽  
Mei Wu ◽  
Longxin Sun

AbstractThe electrochemical behavior of gold dissolution in the Cu2+–NH3–S2O32−–EDTA solution has been investigated in detail by deriving and analyzing the Tafel polarization curve, as this method is currently widely implemented for the electrode corrosion analysis. The dissolution rate of gold in Cu2+–NH3–S2O32−–EDTA solution was determined based on the Tafel polarization curves, and the effects of various compound compositions in a Cu2+–NH3–S2O32−–EDTA mixture on the corrosion potential and corrosion current density were analyzed. The results showed that the corrosion potential and polarization resistance decreased, whereas the corrosion current density increased for certain concentrations of S2O32−–NH3–Cu2+ and EDTA, indicating that the dissolution rate of gold had changed. The reason for promoting the dissolution of gold is also discussed.


Metals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1194
Author(s):  
Philipp Kiryukhantsev-Korneev ◽  
Alina Sytchenko ◽  
Yuriy Kaplanskii ◽  
Alexander Sheveyko ◽  
Stepan Vorotilo ◽  
...  

The coatings ZrB2 and Zr-B-N were deposited by magnetron sputtering of ZrB2 target in Ar and Ar–15%N2 atmospheres. The structure and properties of the coatings were investigated via scanning and transmission electron microscopy, energy dispersion analysis, optical profilometry, glowing discharge optical emission spectroscopy and X-ray diffraction analysis. Mechanical and tribological properties of the coatings were investigated using nanoindentation, “pin-on-disc” tribological testing and “ball-on-plate” impact testing. Free corrosion potential and corrosion current density were measured by electrochemical testing in 1N H2SO4 and 3.5%NaCl solutions. The oxidation resistance of the coatings was investigated in the 600–800 °С temperature interval. The coatings deposited in Ar contained 4–11 nm grains of the h-ZrB2 phase along with free boron. Nitrogen-containing coatings consisted of finer crystals (1–4 nm) of h-ZrB2, separated by interlayers of amorphous a-BN. Both types of coatings featured hardness of 22–23 GPa; however, the introduction of nitrogen decreased the coating’s elastic modulus from 342 to 266 GPa and increased the elastic recovery from 62 to 72%, which enhanced the wear resistance of the coatings. N-doped coatings demonstrated a relatively low friction coefficient of 0.4 and a specific wear rate of ~1.3 × 10−6 mm3N−1m−1. Electrochemical investigations revealed that the introduction of nitrogen into the coatings resulted in the decrease of corrosion current density in 3.5% NaCl and 1N H2SO4 solution up to 3.5 and 5 times, correspondingly. The superior corrosion resistance of Zr-В-N coatings was related to the finer grains size and increased volume of the BN phase. The samples ZrB2 and Zr-B-N resisted oxidation at 600 °C. N-free coatings resisted oxidation (up to 800 °С) and the diffusion of metallic elements from the substrate better. In contrast, Zr-B-N coatings experienced total oxidation and formed loose oxide layers, which could be easily removed from the substrate.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Musa Ahmed ◽  
Ibnelwaleed A. Hussein ◽  
Abdulmujeeb T. Onawole ◽  
Mohammed A. Saad ◽  
Mazen Khaled

AbstractPyrite scale formation is a critical problem in the hydrocarbon production industry; it affects the flow of hydrocarbon within the reservoir and the surface facilities. Treatments with inorganic acids, such as HCl, results in generation toxic hydrogen sulfide, high corrosion rates, and low dissolving power. In this work, the dissolution of pyrite scale is enhanced by the introduction of electrical current to aid the chemical dissolution. The electrolytes used in this study are chemical formulations mainly composed of diethylenetriamine-pentaacetic acid–potassium (DTPAK5) with potassium carbonate; diethylenetriamine pentaacetic acid sodium-based (DTPANa5), and l-glutamic acid-N, N-diacetic acid (GLDA). DTPA and GLDA have shown some ability to dissolve iron sulfide without generating hydrogen sulfide. The effect of these chemical formulations, disc rotational rate and current density on the electro-assisted dissolution of pyrite are investigated using Galvanostatic experiments at room temperature. The total iron dissolved of pyrite using the electrochemical process is more than 400 times higher than the chemical dissolution using the same chelating agent-based formulation and under the same conditions. The dissolution rate increased by 12-folds with the increase of current density from 5 to 50 mA/cm2. Acid and neutral formulations had better dissolution capacities than basic ones. In addition, doubling the rotational rate did not yield a significant increase in electro-assisted pyrite scale dissolution. XPS analysis confirmed the electrochemical dissolution is mainly due to oxidation of Fe2+ on pyrite surface lattice to Fe3+. The results obtained in this study suggest that electro-assisted dissolution is a promising technique for scale removal.


1986 ◽  
Vol 81 (1) ◽  
pp. 189-206 ◽  
Author(s):  
J. Bohrmann ◽  
A. Dorn ◽  
K. Sander ◽  
H. Gutzeit

We determined the extracellular electrical current pattern around Drosophila follicles at different developmental stages (7–14) with a vibrating probe. At most stages a characteristic pattern can be recognized: current leaves near the oocyte end of the follicle and enters at the nurse cells. Only at late vitellogenic stages was an inward-directed current located at the posterior pole of many follicles. Most striking was the observed heterogeneity both in current pattern and in current density between follicles of the same stage. Different media (changed osmolarity or pH, addition of cytoskeletal inhibitors or juvenile hormone) were tested for their effects on extrafollicular currents. The current density was consistently influenced by the osmolarity of the medium but not by the other parameters tested. Denuded nurse cells (follicular epithelium locally stripped off) show current influx, while an accidentally denuded oocyte produced no current. Our results show that individual follicles may be electrophysiologically different, though their uniform differentiation during vitellogenesis does not reflect such heterogeneity.


2005 ◽  
Vol 86 (23) ◽  
pp. 234101 ◽  
Author(s):  
Roberto S. Aga ◽  
Xiang Wang ◽  
Jonathan Dizon ◽  
Jesse Noffsinger ◽  
Judy Z. Wu

2017 ◽  
Vol 744 ◽  
pp. 114-120
Author(s):  
Kyung Man Moon ◽  
Sung Yul Lee ◽  
Jae Hyun Jeong ◽  
Myeong Hoon Lee

In this study, seven types of mortar test specimens were manufactured with parameters, that is, the surface of the reinforced steel bar was treated with hot dip galvanizing (Zn) and the surface of the test specimen was coated with underwater paint, and four types of inhibitors (DAW, MCI, DCI, and Silcon) were added in mortars respectively. And, the seven types of mortar test specimens were immersed in seawater for 4 years. The corrosion properties of the reinforced steel bars embedded in mortar test specimens were investigated using electrochemical methods. The corrosion potentials of the test specimens with painting on the surface of the specimen and Zn coating on the surface of the steel bar exhibited the noblest and lowest values respectively after one year, however, after 4 years, the specimens of underwater painting and of addition of Silcon inhibitor indicated the noblest and lowest values of corrosion potentials respectively. Furthermore, the painting specimen exhibited the smallest values of corrosion probability as welll as of the corrosion current density, while, addition of MCI inhibitor showed the highest values of both corrosion probability and corrosion current density. Moreover, the painting specimen showed the smallest value of neutralization degree among all the specimens, and the largest value of neutralization degree was observed at the specimen of natural condition (no adding of inhibitor, no painting and no Zn coating). As a result, it is considered that the addition of inhibitors, coating with hot dip galvanizing (Zn), and painting on the surface have the effects not only to inhibit the neutralization degree but also to increase the corrosion resistance of the embedded steel bar.


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