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Federal Highway Administration > Publications > Research > Structures > Long-Term Performance of Epoxy-Coated Reinforcing Steel in Heavy Salt-Contaminated Concrete |
Publication Number: FHWA-HRT-04-090 |
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Table 5 describes the test slabs employed in this study. The ECR specimens from the 96-week SE test that remained for extended outdoor exposure were coated with six different powder coating products, which were manufactured by Akzo, O'Brian, 3M, and Ajikawa (Japanese). Individual coatings were identified as Akzo-Grey TM, Akzo-GreenTM, Akzo-OliveTM, O'Brian GoldTM, 3M 213TM, and AjikawaTM. They are randomly designated as coatings A through F in this report. This nomenclature is identical to that in Report No. FHWA-RD-98-153.[4] As summarized in table 5, the slabs were classified into four configuration groups. These were (1) slabs containing ECR in the top mat and black bar in the bottom mat (ECR top-black bottom, 19 slabs); (2) slabs containing ECRs in both mats (ECR top-ECR bottom, 6 slabs); (3) control slabs containing black bars in both mats (black top-black bottom, 3 slabs); and (4) slabs containing straight stainless steel bars coupled with either black or stainless steel bottom bars (stainless steel, 3 slabs). Among the 19 ECR top-black bottom slabs, 6 had two 180-degree bent ECRs in the top mat, and the concrete cover of another 7 slabs was precracked over the straight bars. One specimen of each black top-black bottom and stainless top-black bottom slabs contained 180-degree bent bars in the top mat. In addition, one black and stainless slab had precracks over the top mat bars. None of the ECR top-ECR bottom slabs contained bent bars or precracks.
Every ECR bar was intentionally damaged by drilling holes through the coating to represent either 0.004 or 0.5 percent artificial coating defect using two different drill bit sizes. In every ECR top-ECR bottom slab, the two top mat ECRs contained different defect sizes, and a top mat ECR was paired with two bottom mat ECRs containing the same size of defect.
Corrosion progress of the top bar was monitored by both short-circuit potential (SCP) and macrocell current. SCP was measured when top and bottom bars were electrically connected. On the other hand, macrocell current was measured as the voltage drop across a 10-Wresistor connected between the top and bottom bar mats. The current data then were converted into macrocell current density according to Ohm's law and a known surface area of 145.7 cm2 (22.6 in.2) for the anode (top bar). The same area was used for both coated and uncoated steel. Test data was collected periodically. During the last data measurements, additional data were collected, including the open-circuit potential (OCP) of top mat bars after the top and bottom mat bars were disconnected, the AC resistance between the top and bottom mats, and the impedance modulus (|Z|) at 0.1 Hertz (Hz) of top mat bars using Electrochemical Impedance Spectroscopy (EIS). Before autopsy, researchers documented the exterior condition of the test slabs using a digital camera. Photographs of the test slabs are provided in appendix A.
Autopsies were conducted in groups of four or five test slabs. A detailed autopsy of each slab was performed according to the following procedures:
Autopsy procedure for ECR
The elapsed time between steps 6 and 11 did not exceed 1 week.
Autopsy procedure for black bars and stainless steel bars
The elapsed time between steps 6 and 8 did not exceed 1 week.
Concrete powder samples were taken by drilling with a 9.5-mm (3/8-inch) diameter masonry drill bit along the reinforcing steel imprints in the top mat of every slab. In addition, 14 powder samples were also collected from the selected bar imprints in the bottom mat. These powder samples were analyzed for water-soluble chloride concentration according to ASTM C1218 to determine the chloride content readily available at the bar depth. Based on the water-soluble chloride concentration analysis results, 23 samples (15 from top mat and 8 from bottom mat) were further selected and analyzed for acid-soluble chloride concentration according to ASTM C1152 to determine a relationship of water-soluble versus acid-soluble chloride concentrations.