Research Article  Open Access
Muhammad Rafique, Nasir M. Mirza, Sikander M. Mirza, Kimberlee J. Kearfott, Shahab A. Abbasi, Syed F. Naeem, "Parametric Study of TimeDependent Corrosion Product Activity due to ^{56}Mn, ^{58}Co, and ^{60}Co in the Primary Coolant Circuit of a Typical Pressurized Water Reactor", Journal of Chemistry, vol. 2015, Article ID 809672, 10 pages, 2015. https://doi.org/10.1155/2015/809672
Parametric Study of TimeDependent Corrosion Product Activity due to ^{56}Mn, ^{58}Co, and ^{60}Co in the Primary Coolant Circuit of a Typical Pressurized Water Reactor
Abstract
Results of a detailed study, based on the parametric analysis of activated corrosion products, in primary coolant of a typical pressurized water reactor (PWR) are presented. The parameters influencing time dependent buildup of corrosion product activity (CPA) in primary coolant loop of PWR were identified. The computer program CPAIR was used to accommodate for time dependent corrosion rates. The behaviors of ^{56}Mn, ^{58}Co, and ^{60}Co were studied over the reactor operational time. During the course of normal operation of reactor, the CPA is dominated by ^{56}Mn, while ^{58}Co and ^{60}Co are the predominant radionuclides after reactor shutdown. Parametric study suggests that the total CPA is most sensitive to ionexchanger removal rates. For a removal rate of 300 cm^{3}s^{−1}, the specific activity due to ^{56}Mn has the maximum value of 3.552 × 10^{4} Bqm^{−3} after 1,000 hours of reactor operation. This value decreases drastically to 8.325 × 10^{3} Bqm^{−3 }at removal rate of 900 cm^{3}s^{−1}. Additionally, CPA due to ^{56}Mn, ^{58}Co, and ^{60}Co shows strong dependence on removal rates from the core material surfaces. Variations in the values of radionuclide removal rates from piping surface and radionuclide removal rate from deposition on pipes showed only very small effects on CPA buildup.
1. Introduction
Corrosion products activated by high neutron flux in the reactor core are the dominant contributors to the postshutdown radiation field (PSRF) for all water reactors. Pressurized water reactors (PWRs) have an order of magnitude higher PSRF values compared to gascooled reactors. Large PSRF values affect the plant availability factor by prolonging repair and maintenance schedules, entailing annual economic penalties of several billion US dollars [1].
In the past, several authors [2–18] carried out investigations on the formation, transport, and deposition of radioactive corrosion products in various parts of PWRs. Several models were developed to simulate corrosion product transport and the buildup of activity in the primary coolant systems of PWRs. The PACTOLE program [4] was developed for predicting the timedependent behavior of the activation of PWR corrosion products. Based upon experimental data, the CORA code was upgraded in 1985 [19] to model the transport of corrosion products in primary coolant loop of PWRs. The MIGA code was developed [20] on a strong understanding of the chemical thermodynamics that determines the most stable oxide phase likely to exist under the chemistry and temperature conditions in each region of the primary circuit. The DISER program [21] simulates corrosion product activity (CPA), assuming that the coolant contains solute, colloids, and particulate corrosion products. Song and Lee [22] investigated the generation mechanism of crud in the long term fuel cycle, using the COTRAN code, which simulates the behavior of the crud based on double layer concept model and solubility difference. The effects of flow and power transients on CPA were investigated by Mirza et al. and Deeba et al. using the code CPAIR [23, 24]. This was further modified to account for CPA under linearly and nonlinearly rising corrosion rate models by Mirza et al. [13, 14] and Rafique et al. [15].
Malik et al. [25] studied CPA under flow rate transients, having extended burnup cycles with timedependent pHlevel and boric acid variations. Their finding showed CPA buildup towards saturation following the mixing of boron in primary coolant and a decreasing trend following an increase in pH value. Another study by Malik et al. [26] showed that the use of enriched boric acid as chemical shim actually lowers the primary coolant activity when higher pH values are employed in coolant rather than natural boric acid.
Lewis et al. [27] developed a physical model describing the coolant activity behavior of ^{99}Tc during constant and reactor shutdown operations. Kang and coworkers [19] investigated the inventory of radioactivity in the typical 1,000 MWe Spanish PWR. Analysis was based on DORT models. Henshaw and coworkers [28] proposed a model for simulating thermal hydraulic and chemical conditions within fuel crud deposits. The unique feature of their model is that the chemistry is coupled to the thermohydraulics via the increase in the saturation temperature with the concentration of dissolved species. The model explains several crud scrape observations.
Particulate fouling due to corrosion product sedimentation plays an important role in heat exchanger material integrity and water chemistry. Zebardast et al. [29] proposed a new experimental method for the detection of magnetite particles at temperatures up to 473 K.
Inpile loops were used for the experimental study of possible improvements in the coolant chemistry for reducing the corrosion product dose rates [30, 31]. Those studies indicated that dissolution and crystallization cannot be modeled accurately enough in the absence of the required experimental coefficients for these processes. Those detailed studies revealed that the rate of corrosion in the reactor systems continues increasing as the time of reactor operation at full power increases. Access and frequent maintenance to areas near primary pumps then become very limited due to high radiation doses from primary water and pipe scale.
In this work, parametric studies of CPA under normal reactor operation were carried out. The three radionuclides ^{56}Mn, ^{60}Co, and ^{58}Co were considered. Sensitive parameters are identified from the models, showing their effects on CPA buildup in the primary coolant of typical PWRs.
2. Mathematical Models
The purpose of the parametric analysis of CPA in the primary coolant loop of PWRs is to study the sensitivity of the model simulations to uncertainties in the values of model input data. This work identifies sensitive parameters occurring in mathematical models used for simulating the behavior of CPA.
The governing timedependent differential equations for modeling CPA in the primary circuits of PWRs appear in the literature [13–16, 18, 23, 24] and now are summarized. The rate of buildup of target nuclide concentration in coolant water can be written aswhereand the quantities , , , and are removal rates due to ionexchanger, deposition on pipes, deposition on core surfaces, and removal by filters, respectively. Similarly, the leakage rate from the th leak is given by , where the term is the rate at which primary coolant loop loses water from its th leak (cm^{3}s^{−1}). In addition, , where is the rate at which isotopes are removed from the scale on piping (cm^{3}s^{−1}), and , where is the rate at which isotopes are removed from the scale on core material (cm^{3}s^{−1}).
In the above equations (the radionuclide removal rates due to ionexchanger, deposition on pipes, deposition on core surfaces, and removal by filters), (leakage rate from the th leak), (radionuclide removal from piping surface), and (radionuclide removal rate from scales on core materials) are sensitive variables which change the timedependent CPA in the primary coolant of PWR.
If is the group constant for the production of isotope from target nuclide, then , the effective group flux (neutronscm^{−2}s^{−1}), is defined by the equation
The values of decay constant () for ^{56}Mn, ^{60}Co, and ^{58}Co are provided in Table 1. The group flux is averaged over the geometry of the core and has been estimated using LEOPARD [32] and ODMUG [33] programs in the CPAIR. The times and are the core residence and loop times, respectively.

The core residence time is given bywhere is the core height, is the flow crosssectional area in (cm^{2}), is the coolant density at operating temperatures, and is the timedependent flow rate (gs^{−1}).
The loop time is approximated as for the complete loop length . , , and stand for the target nuclide concentration in water, on piping surfaces, and on core surfaces (atomscm^{−3}); is flow rate perturbation parameter, defined as , where is the timedependent flow rate and is the steady state flow rate under normal operations. Because in this study transient conditions are avoided, in our subsequent study we will take value of equal to unity; that is, . is primary coolant volume.
The corrosion source term appearing in the above equation is given bywhere is the timedependent corrosion rate (gram cm^{−2}s^{−1}), is the area of system exposed to coolant for corrosion, is Avogadro’s number (6.023 × 10^{23} atoms gmole^{−1}), and is the atomic weight of the target nuclide (g). Here, and are abundances of target nuclides and chemical elements in the system, respectively.
The rate of change of active material concentration in primary coolants for each radionuclide is given bywhere , , and are the concentrations of the activated radionuclides in the primary coolant water, on the piping, and on the core surfaces, respectively, in atomscm^{−3}.
The rate of activity buildup on core scale is given bywhere and .
Here is volume of the scale on the core (cm^{3}). And , where is removal rate from scales on core surfaces. Consider .
The rate of buildup of target nuclide concentration on the core scale, , is given by It then follows that the rate of change of target nuclide on piping walls, , isThe rate of deposition of active materials on the pipes is expressed aswhere , with equal to volume of scale on the piping (cm^{3}). , is removal rate from piping surface (cm^{3}).
The rate of activity buildup in ionexchanger is expressed mathematically aswhere , where is volume of ionexchanger. is removal rate by ionexchanger.
The rate of activity buildup in filters becomeswhere , is volume of filter, and is removal rate of filters.
Using the above set of coupled differential equations ((1) through (12)), the computer program CPAIR (corrosion product activity in reactors) [15], using fourthorder RungeKutta method to find the activity values due to corrosion, was modified for this work.
3. Methods and Assumptions
The computer code CPAIR, utilizing specifications of a typical PWR with power of 1,000 MWe, was considered [13–15, 34]. Initial impurity concentrations were assumed to be zero. The numerical values of experimental fractional exchange rates () and resolution rates () assumed for this work are summarized in Table 2.

The design data values for a typical PWR under consideration are given in Table 3 [13–15, 34]. The core averaged group fluxes have been computed using LEOPARD and ODMUG computer codes. The LEOPARD program is a zerodimensional unit cell computer code with 54 fast and 172 thermal energy groups. Evaluated Nuclear Data (ENDFIV) set has been used in the cross section library. In this work, equivalent cells of a typical PWR [34] have been employed to generate group constants for fuel cells and water holes. These cellaveraged group constants are then used in the onedimensional multigroup diffusion theory based ODMUG code [33]. It calculates the group fluxes as a function of position in the reactor. These group fluxes are subsequently averaged over the core. Both LEOPARD and ODMUG are treated as subroutines of the CPAIR program.

The plant surface area of ~10^{8} cm^{2} is exposed to the primary coolant for corrosion. In the presence of corrosion inhibitors, an equilibrium corrosion rate of 2.4 × 10^{−13} gcm^{−2}s^{−1} [13–15, 33–35] exists after 1 y operation of a reactor with a primary coolant volume of 1.3 × 10^{7} cm^{3}. The corrosion rate of 25 μgs^{−1} has been used as normal equilibrium rate in subsequent studies.
The purification rate due to an ionexchanger was considered to be large enough to regard deposition, resolution, and leakage as secondorder effects. Three radionuclides, ^{56}Mn (soluble corrosion products, coming from impurities in the steel), ^{60}Co, and ^{58}Co (insoluble corrosion products), were considered.
4. Results and Discussion
During normal reactor operation at full power, the major contributor towards activity comes from the radionuclide ^{56}Mn. The ^{56}Mn activity saturates at about 150 h after start of the reactor. The saturation of ^{56}Mn activity was due to the fact that we assumed abundances of target nuclides and chemical elements in the system equal to 1 and 0.5, respectively. Its saturation value is 8.325 × 10^{−3} Bqcm^{−3} and it makes the primary coolant as a 2.453 × 10^{7} Bq source (including coactivity) within 150–230 h of reactor operation at full power.
4.1. Effect of IonExchanger Removal Rates () on CPA Buildup in Primary Coolant Loop
Specific activity due to each of the radionuclides (^{56}Mn, ^{58}Co, and ^{60}Co) changes significantly, in the primary coolant loop, with the assumed removal rates for the ionexchanger.
At removal rate of 300 cm^{3}s^{−1}, the specific activity due to ^{56}Mn reaches a maximum value (saturation value) of 3.552 × 10^{4} Bqcm^{−3} after 1,000 h of reactor operation as shown in Figure 1. Specific activities at removal rates of 400, 500, 600, 700, 800, and 900 cm^{3}s^{−1} result in CPA values of (2.49, 1.868, 1.465, 1.188, 0.984, 0.832) × 10^{4} Bqcm^{−3}, respectively.
These values indicate the fact that ionexchanger removal rates play an important role in controlling the specific activity in PWR primary coolant. So removal rates of 800 cm^{3}s^{−1} and greater are optimal values of ionexchanger removal rate. The parameter is the most sensitive parameter for the mathematical models above. By changing values of there will be considerable change in the coolant activity.
The normalized specific activity due to ^{56}Mn was evaluated using a conventional removal rate of 600 cm^{3}s^{−1}. Specific activity due to ^{56}Mn at removal rates of 300, 400, 500, 700, 800, and 900 cm^{3}s^{−1} was 2.42, 1.7, 1.27, 0.81, 0.67, and 0.57 times the conventional removal rate, respectively. Normalized specific activity as a function of different removal rates is shown in Figure 2.
4.2. Effect of Radionuclide Removal Rate from Core Surface Scale () on CPA Buildup in Primary Coolant Loop
Variations in the value of change the value of CPA in primary circuit of PWR. At cm^{3}s^{−1} the specific activity due to ^{56}Mn in primary coolant becomes 1.21 × 10^{4} Bqcm^{−3}, which decreases at higher values of and becomes 1.16 × 10^{4} Bqcm^{−3} at cm^{3}s^{−1}. The variation of ^{56}Mn specific activity with is depicted in Figure 3 and saturation values are listed in Table 4.
 
Actual experimental value of resolution value for core in a typical PWR. 
Normalized values of specific activities due to ^{56}Mn as a function of different resolutions rates from core surfaces are shown in Figure 4. A conventional value of cm^{3}s^{−1} was chosen and specific activity due to ^{56}Mn at resolution rates of 25, 30, 35, 45, 50, and 55 cm^{3}s^{−1} was found as a factor of 1.019, 1.012, 1.006, 0.99, 0.987, and 0.981 with the conventional chosen resolution rate activity.
Variation in the value of also changes the amount of radioactivity due to ^{58}Co in primary coolant. The specific activity due to ^{58}Co decreases with increasing the values of . For cm^{3}s^{−1} the specific activity due to ^{58}Co has the value 2.11 × 10^{4} Bqcm^{−3} after 1,000 hours of reactor operation, and this value decreases to 0.989 × 10^{4} Bqcm^{−3} at cm^{3}s^{−1} as shown in Figure 5 and Table 4. The resolution rates must also be considered a sensitive parameter.
Normalized values of specific activities due to ^{58}Co as a function of different resolutions rates from core surfaces are shown in Figure 6. A conventional value of cm^{3}s^{−1} was chosen and specific activity due to ^{58}Co at resolution rates of 25, 30, 35, 45, 50, and 55 cm^{3}s^{−1} was found as a factor of 1.56, 1.31, 1.14, 0.89, 0.81, and 0.73 with the conventional chosen resolution rate activity.
Similarly specific activity due to ^{60}Co in primary coolant decreases with increasing values of . For cm^{3}s^{−1} the specific activity has the value 432 Bqcm^{−3} after 1,000 h of reactor operation. This value decreases to 199 Bqcm^{−3} at cm^{3}s^{−1} as shown in Figure 7 and Table 4.
4.3. Effect of Radionuclide Removal Rate from Core Surface Scale () on CPA Buildup on Piping Surface
Activated corrosion products once produced may get deposited on piping surfaces of primary coolant loop over the period of reactor operation, thereby becoming the potential source of radiation field. On piping surfaces of primary coolant loop the value of specific activity due to ^{58}Co for cm^{3}s^{−1} has the value 5.81 × 10^{4} Bqcm^{−3} after 1,000 h of reactor operation, and this value decreases radically to 2.838 × 10^{4} Bqcm^{−3} at cm^{3}s^{−1} as shown in Figure 8.
On piping surfaces of primary coolant loop the value of specific activity due to ^{60}Co for cm^{3}s^{−1} has the value 4847 Bqcm^{−3} after 1,000 h of reactor operation, and this value decreases radically to 2331 Bqcm^{−3} at cm^{3}s^{−1}, as illustrated in Figure 9.
4.4. Effects of Radionuclide Removal Rate from Piping Scales () on CPA Buildup in Primary Coolant Loop
While changing the value , change in CPA in primary coolant has been observed. For the CPA due to ^{58}Co has value 3626 Bqcm^{−3}, which decreases to 3589 Bqcm^{−3} at as shown in Figure 10. Similarly for ^{60}Co specific activity has the value 270 Bqcm^{−3} at , and this value decreases to the value 266 Bqcm^{−3} at as shown in Figure 11 and Table 5.
 
Actual experimental value of resolution rate for piping in a typical PWR. 
4.5. Effects of Removal Rate from Deposition on Piping Surfaces () on CPA Buildup in Primary Coolant Loop
Effect of on CPA due to ^{58}Co and ^{60}Co in primary coolant has also been studied. For ^{58}Co the specific activity has the value 3697 Bqcm^{−3}, and this value decreases to 3589 Bqcm^{−3} for after 1,000 h of reactor operation, as shown in Figure 12 and Table 6. For ^{60}Co the specific activity has the value 277 Bqcm^{−3}, and this value decreases to 268 Bqcm^{−3} for after 1,000 h of reactor operation, as shown in Figure 13.
 
Actual experimental value of resolution rate from deposition on piping. 
Some of the results of CPAIR have been compared with the code CRUDSIM/MIT [31]. The same data were used to simulate the CPA using CPAIR program, resulting in 2.02 × 10^{4} Bqcm^{−3} estimated for the stainless steel letdown filters, whose function is to retain corrosion products ^{58}Co, ^{60}Co, and ^{56}Mn. Because solubility is a function of temperature and the temperature of the filters is less than that of the bulk coolant, the filter activity concentrations are not necessary representatives of actual coolant activity concentrations. The filter results, however, are very similar to the value of 1.85 × 10^{4} Bqcm^{−3} reported elsewhere [31].
5. Conclusions
Corrosion products are strong contributors to radiation levels produced in personnel working environment of PWR, and thus the estimation of corrosion product activity (CPA) is important. Higher burnup, longerlived reactor cores make the problem more critical. In this work, a parametric study of CPA in primary coolant of a typical PWR was carried out using the CPAIR computer code. Conclusions based upon those numerical simulations include the following.(i)During normal operation ^{56}Mn dominates the CPA, while ^{58}Co and ^{60}Co are the main contributors after shutdown.(ii)The CPA shows a strong sensitive dependence on .(iii)The variation in other parameters, including , , and , only weakly affects the CPA.(iv)Excellent agreement was found between predictions of CPA using a modified version of CPAIR and CRUDSIM/MIT findings.
Nomenclature
:  Target nuclide concentration in primary coolant water, atomscm^{−3} ((1), (8), and (9)) 
:  Target nuclide concentration on inner walls of the piping, atomscm^{−3} ((1) and (9)) 
:  Target nuclide concentration on core surfaces, atomscm^{−3} ((1) and (8)) 
:  Radionuclide concentration primary water, atomscm^{−3} ((6), (7), (10), (11), and (12)) 
:  Radionuclide concentration on the piping, atomscm^{−3} ((6) and (10)) 
:  Radionuclide concentration on the core surface, atomscm^{−3} ((6) and (7)) 
:  Removal rate due to ionexchanger (1) 
:  Removal rate from deposition on pipes (1) 
:  Removal rate from deposition on core surfaces (1) 
:  Removal rate by filters (1) 
:  Primary coolant loop water loss rate from the th leak, cm^{3}s^{−1} (1) 
:  Radionuclide removal rate from pipe scale, cm^{3}s^{−1} (1) 
:  Radionuclide removal rate from core surface scale, cm^{3}s^{−1} (1) 
:  Corrosion source term (5) 
:  Timedependent corrosion rate, gcm^{−2}s^{−1} (5) 
:  Area of system exposed to coolant for corrosion, 10^{8} cm^{2} (5) 
:  Avogadro’s number, 6.023 × 10^{23} atomsg^{−1}mole^{−1} (5) 
:  Target nuclide atomic weight (5) 
:  Target nuclide abundance of target nuclide in system (5) 
:  Chemical element abundance of chemical element in system (5) 
:  Volume of the scale on the core, cm^{3} 
:  Volume of scale in the piping, cm^{3} 
:  Coolant water volume, cm^{3} ((1) and (5)) 
:  Thermal neutron flux averaged over the core geometry, neutronscm^{−2}s^{−1} (3) 
:  The group constant for radionuclide production from target nuclides 
:  The effective group flux, neutronscm^{−2}s^{−1} 
:  Steady state flow rate under normal operations (4) 
:  Timedependent flow rate (4). 
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
Acknowledgment
Muhammad Rafique is grateful to the Higher Education Commission of Pakistan for providing postdoctoral fellowship in the form of Grant 26(22)/PDFP/HEC/2013/14.
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Copyright © 2015 Muhammad Rafique et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.