Abstract
This paper presents modelling results on the RBMK-1500 reactor water purification and cooling system (PCS) components contamination at Ignalina NPP Unit 1. The modelling was performed using a computer code LLWAA-DECOM (Tractebel Energy Engineering, Belgium), taking into consideration PCS components characteristics, parameters of the water flowing in circuits, system work regimes, and so forth. During the modelling, results on activity of PCS subsystems and components’ deposits and nuclide composition of deposits at the moment of the final shutdown of the reactor, as well as activity decay of the most contaminated PCS components’ deposits and dose rates after the final shutdown of the reactor, were obtained. Significant difference of contamination levels was revealed among PCS subsystems and subsystems components. The subsystem of nonpurified water is the most contaminated in PCS, and the activity of the least contaminated component in this subsystem is only 1.42% compared to the activity of the most contaminated component. The most contaminated and the least contaminated components of the purified water subsystem comprise 28.33% and 0.86% of activity, respectively, compared to the activity of the most contaminated PCS component.
1. Introduction
On December 31, 2009, after the final shutdown of Unit 2 (Unit 1 was closed down on December 31, 2004), Ignalina Nuclear Power Plant (INPP) terminated generation of electricity. After that the decommissioning is its main activity. In order to plan the dismantling process, data about the contamination levels, nuclide composition, amount of the decommissioning radioactive waste, and so forth, are necessary. Contamination of the systems components with radioactive particles is a result of the contaminated cooling liquid (water at INPP) circulating within these systems.
There are several possibilities for the main circulation circuit (MCC) and purification and cooling system (PCS) water to be contaminated with activation products [1]. But usually corrosion of the components is the most important problem. Intensity of corrosion in the reactor components depends on many factors, for example, temperature, composition of components and duration of operation, coolant flow regime, and so forth. Formation process of corrosion products and transfer mechanisms are described in detail in [2–5].
The corrosion products of systems components are transferred by the coolant to the reactor active zone. Here they form deposits on the surfaces of the equipment and are activated by high neutron fluxes. Due to erosion, these activated particles pass to the coolant, and due to its circulation they are deposited on the surfaces of the equipment located outside the reactor’s active zone. Corrosion particles may not deposit on the walls of the equipment in the active zone, but they are activated during circulation through the active zone and form a layer of contaminated deposits on the surfaces of the equipment located outside the boundaries of the active zone [6]. Corrosion and erosion products of the activated equipment located in the active zone are another source for contamination of the equipment. In case there are defects in fuel rods, fission products in the nuclear fuel can migrate through damaged fuel claddings and pass to the coolant flowing in MCC. Fission products are also additionally generated during the fission of “tramp” uranium, whose particles are deposited on the outside of the fuel components’ claddings (contaminated during manufacturing of the fuel). During operation, the coolant could be contaminated with these particles too [7]. Spectrum of the fission products of the “tramp” uranium is analogous to the spectrum of fission products in nuclear fuel. Radioactive contamination of the components is surface contamination since the activated particles deposit on the surfaces of the equipment.
The paper provides modelling and analysis results on activity of the PCS components at Ignalina NPP Unit 1 and deposits nuclide composition as well as variation of the most contaminated PCS components’ deposits activity and their emitted dose rate after the final shutdown of the reactor.
2. Purification and Cooling System (PCS)
PCS maintains the quality of the water in the main circulation circuit as it cleans up the MCC water from corrosion products and soluble salts and controls radioactivity level in the MCC water. Moreover, PCS supplies water to the reactor in case of a shutdown or an emergency, washing MCC system during maintenance of the reactor, and saves precooled water to 50°C in a water-storage tank for start-up of the reactor [8]. Considering contamination of water, the PCS can be classified into three subsystems: nonpurified water, purified water, and additional cooling water. Figure 1 demonstrates a simplified technological scheme of PCS.
PCS consists of pipes from separator drums and pressure headers (1, 5), two mechanical filters in front of the pumps (2), two pumps (4), two regenerators each having six bodies (7), two additional cooler blocks (26), five cartridge (perlite) filters (14), two mix bed (ion-exchange) filters (17), and a filter trap (19).
During normal operation of the reactor, a part of MCC water is supplied to PCS (5) from MCC pressure headers and passes to the regenerators (7, 8) where it is cooled from 265°C to 68°C by the flow of the returning purified water. Operating temperature of the ion-exchange filters is up to 60°C; thus the water of 68°C temperature is additionally cooled to 50°C in the additional cooling subsystem (25, 26, 27). Further, water passes to the mechanical perlite filters (14) by the pipes (13, 15) where corrosion products are removed. Soluble salts and radioactive fission products are removed from the water in ion-exchange filters (17). The purified water is supplied again to the regenerators (7, 8) through the pipe (21). Here it is preheated up to 247°C temperature by the water flowing from MCC pressure headers. Finally, it reaches the MCC separator drums through the pipe (24).
The main PCS components are also listed in Table 1.
3. Methodology
While modelling radioactive contamination of the reactor systems, there are a number of complicated processes (formation of contamination particles and their transfer and relaxation) that must be evaluated. During detailed analysis of the processes, complicated mathematical models and their numerical solution algorithms, requiring considerable calculation resources, are used. Due to this, simplifications are made while evaluating radioactive contamination of the systems in reactors; that is, empirical and semiempirical models and codes (PACTOLE [9], CRUDTRAN [10], ACE-II [11], etc.) are used.
A computer code LLWAA-DECOM (Tractebel Energy Engineering, Belgium) was used for the modelling of radioactive contamination of PCS components. LLWAA-DECOM validation results are presented in [12]. It is demonstrated that there is rather good correlation between predicted and measured dose rates and deposited activities results. When performing modelling, the following input data are necessary: (i)operation characteristics of the system (number of operating cycles, duration of operating cycles), (ii)circulating water parameters (water pH, temperature, average rate, and volumetric activity), (iii)characteristics of contamination particles (density, diameter, and solubility), (iv)design parameters of the system components (design materials, geometric dimensions of the component, and roughness of the walls), and so forth.
Nuclide activity variation of the deposits on the wall of the system component is described using the following equation [12]: where is surface activity of th nuclide on the wall, Bq/m2; is particles deposition rate, m/s; is volumetric activity of th nuclide in the flux, Bq/m3; is soluble part of th nuclide in the circulating agent; is particle relaxation coefficient, ; is decay constant of th nuclide, ; is time. Deposition and relaxation coefficients depend on coolant characteristics (flow rate, temperature, Reynolds number, etc.), characteristics of the system equipment (geometry, roughness of the inner walls, and friction coefficient), and characteristics of radioactive particles (particles density in the coolant, diameter).
In LLWAA-DECOM nuclide activity in the deposits and dose rate at the outer surface can be evaluated for one component during one calculation cycle. Based on PCS Scheme 27 components (Table 1) different characteristics were chosen for evaluation.
4. Results
Analysis of modelling results on PCS components contamination shows that the pipes from MCC pressure headers to the PCS pumps (PCS-5) and also inlet pipes from the pumps to the regenerators (PCS-6) are the most contaminated components in the PCS nonpurified water subsystem (Figure 2(a)). The inner surface of the regenerator pipes (PCS-22) and the pipes of returning water to separator drum (PCS-23, PCS-24) are the most contaminated components in the PCS purified water subsystem (Figure 2(b)). In the additional water cooling subsystem of PCS, the pipes to and from the additional cooler (PCS-27) (Figure 2(c)) are the most contaminated components.
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As Figure 2(a) demonstrates, there is a significant contamination level difference between PCS-5, PCS-6, and other PCS nonpurified water (NV-1) subsystem components. This is because the coolant temperature is higher in heat exchanger. Contamination level of PCS purified water (NV-2) subsystem components is lower (Figure 3(a)) because water passing through the filters is purified. Additional water cooling (NV-3) subsystem contamination level is very low (Figure 3(a)) because the water of this subsystem does not mix directly with water of NV-1 and NV-2 subsystems. Some components (e.g., PCS-7 and PCS-22 or PCS-11 and PCS-26) in the heat exchanger have very different contamination levels on their inner and outer surfaces (Figure 2), since one surface is washed by contaminated water while the other contacts with purified or noncontaminated water.
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Figure 3(a) shows that contamination of PCS subsystems and their components is very different. Activity of the deposits of the least contaminated component in the nonpurified water subsystem (NV-1) is only 1.42% compared to the activity of the most contaminated component. The most contaminated and the least contaminated components of the purified water subsystem (NV-2) comprise 28.33% and 0.86% of activity, respectively, compared to the activity of the most contaminated NV-1 component. Meanwhile, activity of the additional water cooling subsystem (NV-3) component comprises only 0.0005 per cent compared to activity of the most contaminated component of NV-1.
Figure 3(b) shows distribution of relative activity of MCC and PCS subsystems most and least contaminated components, compared to MCC characteristic component (main circulation pump activity). Analysis of the data [13] revealed that the contamination levels of MCC specific components in the reactor active zone and in the separator drums parts filled with water are the highest. So, for comparison purposes, the MCC main circulation pump was selected as it is a more typical component of this system. As can be seen, contamination levels are very different among MCC. The activity of the least contaminated component of MCC is only 7.44% compared to the contamination of the pump. The subsystem of nonpurified water (PCS NV-1) is characterised by 26.37% relative activity for the most contaminated component and 0.37% relative activity for the least contaminated component compared to the contamination of the MCC main circulation pump. The most contaminated and the least contaminated components of the purified water subsystem (PCS NV-2) constitute 7.47% and 0.23% of activity, respectively, compared to the activity of the MCC main circulation pump. Meanwhile, activity of the additional water cooling subsystem (PCS NV-3) component constitutes only 0.00013 per cent compared to activity of the MCC main circulation pump.
As can be seen from Figures 4(a), 4(b), and 4(c), contamination of water is mostly determined by Cs-134 (PCS NV-1 and PCS NV-3 ~31% and PCS NV-2 ~50% of total contamination) and Cs-137 (PCS NV-1 and PCS NV-3 ~22% and PCS NV-2 ~35% of total contamination). The dominant nuclide in deposits is Fe-55: PCS NV-1 subsystem ~56%–~59% of total contamination (Figure 4(a)), PCS NV-2 subsystem ~55%–~56% of total contamination (Figure 4(b)), and PCS NV-3 subsystem ~58% of total contamination (Figure 4(c)). In the water, Fe-55 constitutes only ~5%–~16% of total contamination. So there is a big difference in nuclide composition in water and in deposits (Figure 4). Such difference in nuclide distribution in water and deposits is determined by nuclide solubility in water. Only undissolved part of the nuclide deposits on the surface. Hence, Fe-55 concentration in deposits is considerably higher compared to Cs-134 and Cs-137, although Cs-134 and Cs-137 have higher concentrations in water than Fe-55. This is due to higher solubility of Cs-134 and Cs-137 in water compared to Fe-55. Cs-134 and Cs-137 species are deposited not only on PCS-23 (Figure 4) but on all other components as well. Their input to total activity for most cases is less than 1%; therefore they are under the legend “Other.” Moreover, PCS components PCS-18 to PCS-24 are after filters (subsystem of purified water) and corrosion nuclides are filtered better than fission nuclides; therefore relative activity of Cs nuclides is increased.
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The nuclide composition of deposits changes with time due to different nuclides decay. Figures 5(a) and 5(b) demonstrate nuclide composition variation of deposits on the walls of the two most contaminated components of the PCS subsystem. After 35 years, contamination of the PCS components is highly determined by a long-lived nuclide Ni-63, since short-lived nuclides decay in a short time (Fe-55, Fe-59, Co-58, Co-60, and Mn-54). The contribution of other long-lived nuclides to the total contamination increases also as their activity practically remains unchanged.
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During dismantling, the most important nuclides are those that determine the dose rate by γ radiation from contaminated components. The activity of short lived nuclides is significantly decreasing with time, so the dose rate is decreasing too (Figures 6 and 7). At the moment of the final shutdown of the reactor, γ radiation from contaminated PCS components is mostly determined by Co-60, by Fe-59 and Mn-54, and by Co-60 after 5 years after the shutdown (Figures 6(a) and 6(b)). After several decades contribution of Nb-94 and Cs-137 to the dose rate increases and contribution of Co-60 decreases significantly. Although after some time Ni-63 has the biggest contribution to the activity of the deposits, it is a weak β-emitter; thus, Ni-63 has no practical influence on the dose rate.
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Analysis shows that the contribution to the dose rate from the contaminated water in PCS is much lower compared to the contribution of the deposits. Thus, modelled and measured dose rate values can be compared without the need to remove the coolant from the system. The water is removed from the system prior to dismantling works.
As it is shown in Figure 7, the dose rate decreases significantly (by ~70%) after five years after the final shutdown of the reactor. This is caused by decay of short-lived radionuclides Fe-55, Co-58, and Mn-54. The PCS dismantling works will not start right after the final shutdown of Unit 1. This is related to the strategy of the spent nuclear fuel management. It will be transferred to the dry storage facility only, at least, after 5 years in the pools. Thus such significant decrease of dose rate will allow performing dismantling of the installations and radwaste management with lower radiation doses to the workers.
5. Conclusions
After analysis of the modelling results on the contamination of the water purification and cooling system (PCS) components, the following conclusions have been drawn.(1)Contamination of PCS subsystems and their components is very different. Activity of the deposits of the least contaminated component in the nonpurified water subsystem (NV-1) is only 1.42% compared to the activity of the most contaminated component. The most contaminated and the least contaminated components of the purified water subsystem (NV-2) constitute 28.33% and 0.86% of activity, respectively, compared to the activity of the most contaminated NV-1 component. Meanwhile, activity of the additional water cooling subsystem (NV-3) component constitutes only 0.0005 per cent compared to activity of the most contaminated component of NV-1.(2)Nuclide composition of deposits formed on the PCS components differs significantly from circulating water nuclide composition. Cs-134 and Cs-137 are dominant nuclides in the water, while Fe-55, Co-60, and Mn-54 are dominant nuclides in the deposits.(3)Short-lived radionuclides Fe-59 and Mn-54 have the biggest influence on the dose rate at the shutdown of the reactor; five years after the shutdown, Co-60 has the biggest influence. After several decades, Nb-94 and Cs-137 contribute mostly to the dose rate. Due to short-lived radionuclides decay the dose rate decreases significantly over time.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.