Development of Carbonization and a Relatively High-Temperature Halogenation Process for the Removal of Radionuclides from Spent Ion Exchange Resins

This study investigated a two-step thermochemical treatment process consisting of carbonization and halogenation for the removal of radionuclides from spent cation-exchange resin (CER). Based on a thermal analysis of cation-exchange resins, we propose a two-step thermochemical treatment process involving the conversion of spent CER into pyrocarbon and then the removal of radioactive elements from the carbonized CER by converting them volatile halides at very high temperatures. The proposed process mainly consists of a carbonization and halogenation reactor, a UHC (unburned hydrocarbon) combustor, and wet scrubber. A step-by-step experimental and numerical optimization study was conducted with the carbonization and halogenation reactor and the UHC combustor. The optimum operating conditions could be established based on the results of a thermal analysis of the CER, a nonisothermal kinetic analysis, a numerical modeling study of a plug flow reactor (PFR)-type combustor, and a thermodynamic equilibrium analysis of a system consisting of a mix of carbonized CER and halogenation gas. The results of this study present detailed design of a novel multifunctional reactor and operating conditions of a bench-scale carbonization and halogenation process. Basic performance tests using CER doped with nonradioactive Co and Cs, indicated as Cs-137/134 and Co-60/58, were conducted under the optimized conditions. The results of these tests showed that the novel thermochemical process proposed in this study is a viable process that effectively removes radioactive elements from spent CER.


Introduction
Ion-exchange (IE) polymer is an insoluble solid resin that acts as a medium for the ion exchange process. When it comes into contact with a liquid that contains ions in a solution, it exchanges some of its constitutive ions with other ions [1,2]. IE resins are widely used in various separation, purification, and decontamination processes. Both chemical (coal and gas) and nuclear power plants utilize organic IE resins to polish condensate materials within water stream circuits [3]. Over time, these IE resins must be regenerated or replaced. When this happens, the spent IE resins must be disposed of and, as such, spent IE resins are a major fraction of the hazardous organic waste from power plants [4].
Spent IE resins, a type of combustible organic waste, cannot be readily disposed due to problems associated with the emissions of toxic gases and volatile radioactive elements [5,6]. Despite such difficulties, the organic fraction of spent IE resins should be properly decomposed, and the decomposition residue should then be immobilized for safe disposal in a radwaste repository. There have therefore been many studies of the lowtemperature pyrolysis of spent IE resins in the nuclear industry. Brähler and Slametschka (2012) studied low-temperature pyrolysis of spent ion-exchange resins in a pebble bed at approximately 500 • C with keeping radioactive cesium species in the solid pyrolysis residue [7,8]. An earlier study by Peterson and Kemmler (1984) involved the drying of wet spent resins and the pyrolysis of dried powder-type resins at 300-350 • C with keeping radioactive elements in the pyrolysis residue, which in that case was mostly composed of ash and carbon [9]. Matsuda et al. (1987) investigated the influence of functional sulfonic acid group on the pyrolysis characteristics for cation exchange resins [10]. These studies focused on the pyrolysis conditions that allow the retention of radioactive elements in a pyrolysis residue. However, pyrolysis residues bearing radioactive and hazardous elements should be further treated and transformed into a high-integrity waste form that can be safely disposed of in a radwaste repository. These processes result in a significant increase in the volume of the final waste form.
The portion of inorganics, including ion-exchanged radioactive elements and dirt, is at most approximately 2% of dried spent IE resins [11]. Conventional thermal treatment technologies such as incineration and other similar thermal treatment processes, i.e., high-temperature plasma and pyrolysis processes, which combust or gasify most organic constituents in IE resins, have led to valuable reductions in waste volumes. Instead, however, a very large volume of off-gas bearing UHCs (unburned hydrocarbons), acid gases, and toxic and radioactive elements are generated. The emission of these hazardous constituents in the off-gas can be effectively controlled using currently well-developed APCDs (air pollution control devices). However, the use of a very sizable off-gas treatment system, which must become radioactive decommissioning waste itself at the end of its service life, is unavoidable. Generally, this overly significant flaw means such devices cannot be readily commercialized as a radioactive facility.
This work proposes a novel thermochemical decontamination process for spent IE resins conducting a two-stage process of the carbonization of organic constituents and the halogenation removal of radionuclides from carbonized IE resins. The proposed process initially converts the organic constituents of spent IE resins into pyrocarbon. The radionuclides in the carbonized spent resins are then readily removed by converting them into volatile halides in a halogenation atmosphere at higher temperatures. Three key unit processes are carbonization, the combustion of pyrolysis gas during carbonization, and the halogenation removal of radioactive elements in the carbonized resins.
A step-by-step experimental and numerical optimization study for these key unit processes was conducted in this study. An appropriate operation condition for a carbonization reactor was initially determined through a kinetic analysis of the carbonization of cation-exchange resin (CER). The generation of UHCs during the carbonization process was then experimentally investigated. The carbonization of CER generates various aromatic hydrocarbons, such as styrene, toluene, and benzene. Fortunately, these UHCs are key components of commercial liquid fuels such as benzene and toluene; thus, an extensive range of experimental data on the kinetics of combustion reactions for these UHCs is available in the literature [12]. Parametric modeling studies could therefore be conducted to determine an appropriate condition for UHC combustion for the substantial burnout of the UHCs generated during the course of carbonization.
The behavior of radionuclides in the waste thermal treatment process was investigated in a thermodynamic equilibrium modeling study. This was done because a detailed accounting of all possible reactions for inorganic compounds at high temperatures is not available, unlike in the case of the gas-phase combustion mechanisms of organic constituents. Ho et al., investigated the behavior of uranium and plutonium during a thermal treatment of waste under oxidizing and reducing conditions [13]. The behaviors of various radionuclides in irradiated graphite during combustion and hydrothermal oxidation were also investigated by a thermodynamic modelling approach [14]. These equilibrium mod-elling studies were done in an effort to establish a thermal treatment condition that avoids the emission of radionuclides by volatilization. The present study also used a thermodynamic equilibrium modelling study of the behavior of radionuclides under halogenation treatment conditions. On the other hand, however, the present study established the range of the reactor operating condition for the volatilization-related removal of radionuclides by means of thermodynamic modelling.
A bench-scale carbonization and halogenation process was designed and installed based on the results of the experimental and modeling studies of these key unit processes. The capability of this process with regard to the removal of radionuclides from spent resins was demonstrated using non-radioactive surrogates under experimentally and numerically determined appropriate carbonization and halogenation process conditions.

Characteristics of a Target Waste Stream
The target waste stream in this study is spent CER (cation-exchange resin) of the type generated in the nuclear industry. The principal applications of ion exchange processes in nuclear facilities are the removal of contaminants from wastewater effluents and the demineralization of process water streams. A granular type of mixed IE resin with a 1.2:1 cation-to-anion ratio is generally used in nuclear power plants. CER is denser than AER (anion exchange resin). The spent mixed resin bed is conventionally separated by passing water up through the resin bed for fluidization, therefore allowing the denser CER to settle first [11]. It is crucial for the most appropriate method to be applied for each separated spent resin stream after separation. Spent CER bearing metallic radionuclides such Cs-137 and Co-60 is the target waste type in this study. The chemical structure of the strong acidic CE resins used in this study is shown in Figure 1. The ion-exchange mechanisms of two typical ions, a one-valence-count ion (Cs + ) and a two-valence-count ion (Co 2+ ), as examples, are also described in Figure 1.
Processes 2021, 9, x FOR PEER REVIEW 3 of 17 treatment of waste under oxidizing and reducing conditions [13]. The behaviors of various radionuclides in irradiated graphite during combustion and hydrothermal oxidation were also investigated by a thermodynamic modelling approach [14]. These equilibrium modelling studies were done in an effort to establish a thermal treatment condition that avoids the emission of radionuclides by volatilization. The present study also used a thermodynamic equilibrium modelling study of the behavior of radionuclides under halogenation treatment conditions. On the other hand, however, the present study established the range of the reactor operating condition for the volatilization-related removal of radionuclides by means of thermodynamic modelling. A bench-scale carbonization and halogenation process was designed and installed based on the results of the experimental and modeling studies of these key unit processes. The capability of this process with regard to the removal of radionuclides from spent resins was demonstrated using non-radioactive surrogates under experimentally and numerically determined appropriate carbonization and halogenation process conditions.

Characteristics of a Target Waste Stream
The target waste stream in this study is spent CER (cation-exchange resin) of the type generated in the nuclear industry. The principal applications of ion exchange processes in nuclear facilities are the removal of contaminants from wastewater effluents and the demineralization of process water streams. A granular type of mixed IE resin with a 1.2:1 cation-to-anion ratio is generally used in nuclear power plants. CER is denser than AER (anion exchange resin). The spent mixed resin bed is conventionally separated by passing water up through the resin bed for fluidization, therefore allowing the denser CER to settle first [11]. It is crucial for the most appropriate method to be applied for each separated spent resin stream after separation. Spent CER bearing metallic radionuclides such Cs-137 and Co-60 is the target waste type in this study. The chemical structure of the strong acidic CE resins used in this study is shown in Figure 1. The ion-exchange mechanisms of two typical ions, a one-valence-count ion (Cs + ) and a two-valence-count ion (Co 2+ ), as examples, are also described in Figure 1. Chemical structure of the strong acidic cationic ion exchange (IE) resins with functional groups of -SO3H + and ion-exchange mechanisms of two typical ions of a one-valence-count ion (Cs + ) and a two-valence-count ion (Co 2+ ). Chemical structure of the strong acidic cationic ion exchange (IE) resins with functional groups of -SO 3 H + and ion-exchange mechanisms of two typical ions of a one-valence-count ion (Cs + ) and a two-valence-count ion (Co 2+ ).

Principle of the Proposed Process
The principle of the carbonization and halogenation process for the removal of radionuclides from spent CER is shown in Figure 2. Carbon materials are stable, even at very high temperatures, in the absence of oxygen. If we convert spent CER into carbon Processes 2021, 9, 96 4 of 16 materials after removing moisture and volatiles, we can then treat them with halogen gases at very high temperatures. The first step of the proposed process is low-temperature pyrolysis followed by carbonization. During the course of the low-temperature pyrolysis step, moisture and volatiles are removed and the remaining carbon-bearing organics are then converted into pyrocarbon at higher temperatures. During this pyrolysis and carbonization step, captured radioactive metal species such as Cs and Co in the spent CER, as depicted in Figure 1, are converted into their corresponding sulfates or sulfides [15]. The next step is the halogenation treatment of the carbonized spent CER to convert radioactive elements into volatile chlorides. Spent CER contains various types of radionuclides of different origins, including nuclear fuel fission products such as Cs-134, Cs-137, and Sr-90 and activation products such as Fe-59, Co-58, Co-60, Mn-54, Zn-65, and Zr-95. All of these metallic radioactive species remaining in carbonized resins can be removed by converting them into their respective volatile halides by halogenation gases at high temperatures.

Principle of the Proposed Process
The principle of the carbonization and halogenation process for the removal of radionuclides from spent CER is shown in Figure 2. Carbon materials are stable, even at very high temperatures, in the absence of oxygen. If we convert spent CER into carbon materials after removing moisture and volatiles, we can then treat them with halogen gases at very high temperatures. The first step of the proposed process is low-temperature pyrolysis followed by carbonization. During the course of the low-temperature pyrolysis step, moisture and volatiles are removed and the remaining carbon-bearing organics are then converted into pyrocarbon at higher temperatures. During this pyrolysis and carbonization step, captured radioactive metal species such as Cs and Co in the spent CER, as depicted in Figure 1, are converted into their corresponding sulfates or sulfides [15]. The next step is the halogenation treatment of the carbonized spent CER to convert radioactive elements into volatile chlorides. Spent CER contains various types of radionuclides of different origins, including nuclear fuel fission products such as Cs-134, Cs-137, and Sr-90 and activation products such as Fe-59, Co-58, Co-60, Mn-54, Zn-65, and Zr-95. All of these metallic radioactive species remaining in carbonized resins can be removed by converting them into their respective volatile halides by halogenation gases at high temperatures. The granular form of carbonized CER is stable at very high temperatures under a halogenating gaseous condition, such as chlorine and fluorine. However, metals and radionuclides in any other chemical form are converted into their respective volatile halides at high temperatures. If we use chlorine as a halogenating gas, as shown in Figure 2, the sulfate or sulfide forms of radionuclides are converted into their corresponding chlorides. Chlorides of metals and radionuclides have high vapor pressures at high temperatures, and they vaporize into a gaseous stream.
The gas effusion process, the diffusion into micropores of carbon materials, speeds up considerably at higher temperatures. Halogenating gases such as chlorine and fluorine readily diffuse into micropores in the spherical form of carbonized resin and then convert inorganic species into volatile halides. During this process, the major element carbon, C, in the carbonized resins facilitates the halogenation process by taking over oxygen from inorganic compounds. Using the proposed two-step thermochemical process, consisting of carbonization and halogenation, we can readily separate radioactive metal species from spent CER.

Procedure of Experimental and Numerical Modeling Study
The key process units in the proposed process to be optimized to design a benchscale process for trial tests are a carbonization/halogenation reactor for spent CER and an oxidizer for the UHCs (unburned hydrocarbons) generated during the course of the carbonization of CER. The purpose of this experimental and modeling study was to establish The granular form of carbonized CER is stable at very high temperatures under a halogenating gaseous condition, such as chlorine and fluorine. However, metals and radionuclides in any other chemical form are converted into their respective volatile halides at high temperatures. If we use chlorine as a halogenating gas, as shown in Figure 2, the sulfate or sulfide forms of radionuclides are converted into their corresponding chlorides. Chlorides of metals and radionuclides have high vapor pressures at high temperatures, and they vaporize into a gaseous stream.
The gas effusion process, the diffusion into micropores of carbon materials, speeds up considerably at higher temperatures. Halogenating gases such as chlorine and fluorine readily diffuse into micropores in the spherical form of carbonized resin and then convert inorganic species into volatile halides. During this process, the major element carbon, C, in the carbonized resins facilitates the halogenation process by taking over oxygen from inorganic compounds. Using the proposed two-step thermochemical process, consisting of carbonization and halogenation, we can readily separate radioactive metal species from spent CER.

Procedure of Experimental and Numerical Modeling Study
The key process units in the proposed process to be optimized to design a benchscale process for trial tests are a carbonization/halogenation reactor for spent CER and an oxidizer for the UHCs (unburned hydrocarbons) generated during the course of the carbonization of CER. The purpose of this experimental and modeling study was to establish design conditions and the appropriate range of operating conditions of these two key process units.
Step-by-step numerical determination of the operating conditions for these two process units were carried out, and these results were used to design of the bench-scale process for trial tests. The establishment of the carbonization condition of spent CER was initially conducted by means of a kinetic analysis and through a prediction of the carbonization reaction of the CER. Establishment of the operating condition of the UHC combustor for the burnout of the UHCs generated during the carbonization of CER under the optimized condition was then established by a numerical modeling study of a PFR (plug flow reactor) type of combustor. As a final step, an optimum range of the halogenation process conditions for carbonized spent resins was determined.

Analysis of Pyrolysis and Carbonization Steps
A TGA (thermogravimetric analysis) system (SETSYS-Evolution, SETARAM, Lyon, France) was used to investigate the carbonization characteristics of CER. A commercially used form of CER, Amberlite IRN-77 (Rohm and Haas, Philadelphia, PA, USA), with the chemical structure shown in Figure 1, was used in this study. Nonisothermal TGAs with a heating rate of 1 K/min for the CER dried in an oven at 100 • C for 24 h were conducted under an inert atmosphere (>99.999% Ar). The changes in the sample weight and the derivative of the sample weight at elevated temperatures are plotted in Figure 3. Three pyrolysis steps, denoted as R1, R2, and R3, are clearly discriminated by dTG (derivatives of TG, dW/dt) plot. The approximate temperature ranges of R1, R2, and R3 were 50-250 • C, 250-450 • C, and 450-800 • C, respectively. design conditions and the appropriate range of operating conditions of these two key process units.
Step-by-step numerical determination of the operating conditions for these two process units were carried out, and these results were used to design of the bench-scale process for trial tests. The establishment of the carbonization condition of spent CER was initially conducted by means of a kinetic analysis and through a prediction of the carbonization reaction of the CER. Establishment of the operating condition of the UHC combustor for the burnout of the UHCs generated during the carbonization of CER under the optimized condition was then established by a numerical modeling study of a PFR (plug flow reactor) type of combustor. As a final step, an optimum range of the halogenation process conditions for carbonized spent resins was determined.

Analysis of Pyrolysis and Carbonization Steps
A TGA (thermogravimetric analysis) system (SETSYS-Evolution, SETARAM, Lyon, France) was used to investigate the carbonization characteristics of CER. A commercially used form of CER, Amberlite IRN-77 (Rohm and Haas, Philadelphia, PA, USA), with the chemical structure shown in Figure 1, was used in this study. Nonisothermal TGAs with a heating rate of 1 K/min for the CER dried in an oven at 100 °C for 24 h were conducted under an inert atmosphere (>99.999% Ar). The changes in the sample weight and the derivative of the sample weight at elevated temperatures are plotted in Figure 3. Three pyrolysis steps, denoted as R1, R2, and R3, are clearly discriminated by dTG (derivatives of TG, dW/dt) plot. The approximate temperature ranges of R1, R2, and R3 were 50-250 °C, 250-450 °C, and 450-800 °C, respectively. The SEM images of the CER granules, which were pyrolyzed to approximate ending temperatures of R1, R2, and R3 (250 °C, 450 °C, and 800 °C, respectively), are also shown in Figure 3. The first weight loss reaction R1, corresponding to approximately 40% of the initial CER weight, is mainly due to the thermal dissociation of SO2 from polystyrene sulfonate and the vaporization of moisture in the dried CER [15]. The second reaction step R2, corresponding to approximately 20% of the initial CER weight, may be due to the partial decomposition of polystyrene granules. The size of the granules was reduced significantly by shrinkage during the R2 reaction step due to the pyrolysis of polystyrene copolymer upon the emitting of volatile hydrocarbons. No significant reduction in the size The SEM images of the CER granules, which were pyrolyzed to approximate ending temperatures of R1, R2, and R3 (250 • C, 450 • C, and 800 • C, respectively), are also shown in Figure 3. The first weight loss reaction R1, corresponding to approximately 40% of the initial CER weight, is mainly due to the thermal dissociation of SO 2 from polystyrene sulfonate and the vaporization of moisture in the dried CER [15]. The second reaction step R2, corresponding to approximately 20% of the initial CER weight, may be due to the partial decomposition of polystyrene granules. The size of the granules was reduced significantly by shrinkage during the R2 reaction step due to the pyrolysis of polystyrene copolymer upon the emitting of volatile hydrocarbons. No significant reduction in the size of granules was found for the R3 reaction step. This suggests that the third reaction step is the carbonization step. The R3 reaction step continued to approximately 800 • C. Weight loss of approximating 5% was found as a result of this step, although it started at 450 • C and continued for 350 min when ramping up the temperature of the samples from 450 • C to 800 • C. No further weight loss was noted at elevated temperatures exceeding 800 • C. This confirms the R3 reaction step as the carbonization step.
A nonisothermal kinetic analysis and a prediction of the carbonization reaction step, indicated as R3 in Figure 3, were conducted to establish an appropriate carbonization reactor condition. In a nonisothermal system, reaction rates are given as a function of two time-dependent variables: The temperature (T) and the reaction progress (α). This is expressed as where α is the weight reduction fraction, A is the pre-exponential (frequency) factor, E is the activation energy, T is the absolute temperature, R is the gas constant, and f (α) is the reaction model [16]. For the TGA study, α is defined as where m 0 , m t , and m f are the initial weight, the weight at processing time t, and the final weight, respectively. In a nonisothermal heating system with a constant heating rate (dT/dt = B), the reaction rate is given by the following Equation (3): Multiple chemical reactions occur during reaction step R3; thus, precise knowledge of reaction model f (α) is not available. Therefore, a differential isoconversional method, which does not require an explicit assumption of the form of f (α), and constancy of A and E, were used during the kinetic analysis of the nonisothermal TGA data [16]. The differential isoconversional method by Friedman [17] was used in this study. This method is based on the logarithm shown in Equation (3). The values of the kinetic triplets A α , E α , and f (α), which change with the reaction progress α, can be obtained as a function of α by the following Equation (4): The results of the nonisothermal TGAs of the CER with heating rates of 0.5, 1, 1.5, and 2 under an inert atmosphere (>99.999% Ar) are shown in Figure 4a. The reaction rates at different heating rates determined by the nonisothermal TGA data are plotted in Figure  4b. A detailed kinetic study of reaction step R3, which is considered as the carbonization reaction step, was done using the reaction rate data in the temperature range of 400-800 • C.  Plots for the determination of the activation energy Eα and modified pre-exponential factor A′(α) (=Aα f(α)) for reaction step R3 were constructed using Equation (4); these are shown in Figure 5a. The values of Eα and A′(α) determined by the slopes and intercepts of straight lines in Figure 5a are shown in Figure 5b.  Plots for the determination of the activation energy E α and modified pre-exponential factor A (α) (=A α f (α)) for reaction step R3 were constructed using Equation (4); these are shown in Figure 5a. The values of E α and A (α) determined by the slopes and intercepts of straight lines in Figure 5a are shown in Figure 5b. Plots for the determination of the activation energy Eα and modified pre-exponential factor A′(α) (=Aα f(α)) for reaction step R3 were constructed using Equation (4); these are shown in Figure 5a. The values of Eα and A′(α) determined by the slopes and intercepts of straight lines in Figure 5a are shown in Figure 5b.

Establishment of the Carbonization Reactor Condition
An accurate interpretation of the kinetic model is not possible when multiple reactions simultaneously occur because Eα and A′(α) vary with the reaction progress α, as shown in Figure 5b. However, a kinetic prediction for the determination of the time and temperature profile of a reactor to obtain the target reaction progress α when treating the material is possible by applying the determined values of the kinetic triplets (Eα and A′(α) (=Aα f(α)) of any reaction progress α to Equation (5) below.
A set consisting of the reactor temperature and processing time required to complete the progress of carbonization reaction R3 can be established using Equation (5). The progress of carbonization step (reaction step R3) for several different pyrolysis temperature profiles was calculated based on the values of the kinetic triplets shown in Figure 4b using AKTS-Thermokinetics software [18,19]. An example of the optimized pyrolysis condition is shown in Figure 6. If the reactor is heated to 800 °C and sustained for 40 min at 800 °C,

Establishment of the Carbonization Reactor Condition
An accurate interpretation of the kinetic model is not possible when multiple reactions simultaneously occur because E α and A (α) vary with the reaction progress α, as shown in Figure 5b. However, a kinetic prediction for the determination of the time and temperature profile of a reactor to obtain the target reaction progress α when treating the material is possible by applying the determined values of the kinetic triplets (E α and A (α) (=A α f (α)) of any reaction progress α to Equation (5) below.
A set consisting of the reactor temperature and processing time required to complete the progress of carbonization reaction R3 can be established using Equation (5). The progress of carbonization step (reaction step R3) for several different pyrolysis temperature profiles was calculated based on the values of the kinetic triplets shown in Figure 4b using AKTS-Thermokinetics software [18,19]. An example of the optimized pyrolysis condition is shown in Figure 6. If the reactor is heated to 800 • C and sustained for 40 min at 800 • C, carbonization of CER will be completed. Additionally, the progress of the R1 and R2 reactions steps must also be completed during the course of elevating the temperature of the carbonization reactor up to 800 • C. An optimized carbonization condition is the slow heating of the spent CER to 800 • C from 300 • C at a heating rate of 10 K/min to avoid the sudden generation of a large amount of UHCs, and then holding the temperature at 800 • C for 40 min.

UHCs Generated by the Carbonization of CER
The carbonization process generates a significant amount of UHCs, which should be properly decomposed and oxidized into H 2 O and CO 2 . The characteristics of the UHCs generated during the carbonization of CER were investigated using a Py(pyrolysis)-GC/MS (pyrolysis-gas chromatography and mass spectrometer). The instruments used were a portable pyrolyzer (JCI-21) and the HP6890N GC/MS system. The Py-GC/MS result using a pyro-foil at the Curie point temperature of 764 • C are shown in Figure 7. Various types of aromatic hydrocarbons were generated during result pyrolysis of CER. The major UHCs generated were aromatic hydrocarbons. These were C 6 H 6 , C 6 H 5 CH 3 , carbonization of CER will be completed. Additionally, the progress of the R1 and R2 reactions steps must also be completed during the course of elevating the temperature of the carbonization reactor up to 800 °C. An optimized carbonization condition is the slow heating of the spent CER to 800 °C from 300 °C at a heating rate of 10 K/min to avoid the sudden generation of a large amount of UHCs, and then holding the temperature at 800 °C for 40 min. Figure 6. Optimized carbonization reactor heating condition for the completion of carbonization reaction step (R3) with a slow ramping rate to 800 °C to avoid the sudden generation of a large amount of UHCs.

UHCs Generated by the Carbonization of CER
The carbonization process generates a significant amount of UHCs, which should be properly decomposed and oxidized into H2O and CO2. The characteristics of the UHCs generated during the carbonization of CER were investigated using a Py(pyrolysis)-GC/MS (pyrolysis-gas chromatography and mass spectrometer). The instruments used were a portable pyrolyzer (JCI-21) and the HP6890N GC/MS system. The Py-GC/MS result using a pyro-foil at the Curie point temperature of 764 °C are shown in Figure 7. Various types of aromatic hydrocarbons were generated during result pyrolysis of CER. The major UHCs generated were aromatic hydrocarbons. These were C6H6, C6H5CH3, C6H5CH2CH3, and C6H5CHCH2, and their molar compositions based on the peak areas of the GC chromatogram were 7.21%, 15.08%, 12.21%, and 49.08, respectively.

Numerical Determination of the UHC Combustor Operating Condition
A numerical modeling study of the UHC combustor was conducted to design a bench-scale process with a capacity of 5 kg/batch. The simulated conditions for the determination of the UHC combustor operating condition are shown in Figure 8. A cylindrical UHC combustor with a 5 cm inner diameter was assumed as an ideal PFR, in which there is no mixing in the axial direction but perfect mixing in the traverse direction. Parametric model studies of the UHC combustor were performed with ANSYS Chemkin Pro [20]. Chemical kinetic reaction mechanisms for n-alkane hydrocarbons developed by Westbrook et al. [21] were used. The mechanisms were used for the simulation of the combustion of the normalized composition of generated aromatic hydrocarbons (C6H6: 8.6%, C6H5CH3: 18.1%, C6H5CHCH2: 58.7%, and C6H5CH2CH3: 14.6%). It was assumed that SO2 is not involved in the combustion reactions of the UHCs. Based on a treatment rate of 1

Numerical Determination of the UHC Combustor Operating Condition
A numerical modeling study of the UHC combustor was conducted to design a benchscale process with a capacity of 5 kg/batch. The simulated conditions for the determination of the UHC combustor operating condition are shown in Figure 8. A cylindrical UHC combustor with a 5 cm inner diameter was assumed as an ideal PFR, in which there is no mixing in the axial direction but perfect mixing in the traverse direction. Parametric model studies of the UHC combustor were performed with ANSYS Chemkin Pro [20]. Chemical kinetic reaction mechanisms for n-alkane hydrocarbons developed by Westbrook et al. [21] were used. The mechanisms were used for the simulation of the combustion of Processes 2021, 9, 96 9 of 16 the normalized composition of generated aromatic hydrocarbons (C 6 H 6 : 8.6%, C 6 H 5 CH 3 : 18.1%, C 6 H 5 CHCH 2 : 58.7%, and C 6 H 5 CH 2 CH 3 : 14.6%). It was assumed that SO 2 is not involved in the combustion reactions of the UHCs. Based on a treatment rate of 1 kg spent CER/h and a mass loss fraction of the R1 and R2 steps determined by the TGA, as shown in Figure 2, the program input feed rate of gaseous species to the UHC combustor was 0.3 kg/h. The parameters varied for the UHC combustor simulation were the heating temperature, PFR length with a diameter of 5 cm, and equivalence ratio φ (the actual air-UHC ratio to the stoichiometric air-UHC ratio for combustion), as shown in Figure 8.
A numerical modeling study of the UHC combustor was conducted to design a bench-scale process with a capacity of 5 kg/batch. The simulated conditions for the determination of the UHC combustor operating condition are shown in Figure 8. A cylindrical UHC combustor with a 5 cm inner diameter was assumed as an ideal PFR, in which there is no mixing in the axial direction but perfect mixing in the traverse direction. Parametric model studies of the UHC combustor were performed with ANSYS Chemkin Pro [20]. Chemical kinetic reaction mechanisms for n-alkane hydrocarbons developed by Westbrook et al. [21] were used. The mechanisms were used for the simulation of the combustion of the normalized composition of generated aromatic hydrocarbons (C6H6: 8.6%, C6H5CH3: 18.1%, C6H5CHCH2: 58.7%, and C6H5CH2CH3: 14.6%). It was assumed that SO2 is not involved in the combustion reactions of the UHCs. Based on a treatment rate of 1 kg spent CER/h and a mass loss fraction of the R1 and R2 steps determined by the TGA, as shown in Figure 2, the program input feed rate of gaseous species to the UHC combustor was 0.3 kg/h. The parameters varied for the UHC combustor simulation were the heating temperature, PFR length with a diameter of 5 cm, and equivalence ratio ϕ (the actual air-UHC ratio to the stoichiometric air-UHC ratio for combustion), as shown in Figure 8. The concentrations of the fed UHCs at a ϕ value of 0.2 and temperature of 750 °C as a function of the reactor distance are shown in Figure 9a. The reactor length of 16 cm is a critical distance for the substantial destruction of fed UHCs under this condition. Figure  9b shows that various types of other aromatic hydrocarbons were newly formed during The concentrations of the fed UHCs at a φ value of 0.2 and temperature of 750 • C as a function of the reactor distance are shown in Figure 9a. The reactor length of 16 cm is a critical distance for the substantial destruction of fed UHCs under this condition. Figure  9b shows that various types of other aromatic hydrocarbons were newly formed during the thermal decomposition of the fed UHCs. These were also substantially decomposed just before the reactor length of 16 cm. A significant amount of a product of incomplete combustion (PIC), carbon monoxide (CO), however, remained after the reactor length of 16 cm. The carbon monoxide was nearly completely oxidized at the length of ≥20, as shown in Figure 9b.  The reaction pathways of C6H5CH3 and C6H5C2H5 into C6H6 and that of C6H6 into CO2 are depicted in Figure 10. The largest amount of UHC generated by the pyrolysis of CER, with the basic structure of polystyrene, is C6H5C2H5, as shown in Figure 1. C6H5C2H5 is decomposed into C6H6 and CO via C6H5CH2, and C6H5C2H3, respectively, as shown in Figure 10a,b. The C6H5C2H3 was the primary decomposition product of C6H5C2H5. As shown in Figure 10a,b, a significant amount of C6H6 is generated during the course of the thermal decomposition of C6H5C2H5 and C6H5CH3. This explains the delayed decomposition of C6H6 shown in Figure 9a. The concentration of C6H6 was nearly constant to the length of 10 because the decomposition rate of the fed C6H6 is nearly equal to the formation rate of C6H6 due to the decomposition of the fed hydrocarbons until the length of 10 cm. The steep increase in the CO2 concentration during the course of the decomposition of the fed UHCs was due to the rapid increase in the generation of CO with the temperature according to the reaction pathway shown in Figure 10. The reaction pathways of C 6 H 5 CH 3 and C 6 H 5 C 2 H 5 into C 6 H 6 and that of C 6 H 6 into CO 2 are depicted in Figure 10. The largest amount of UHC generated by the pyrolysis of CER, with the basic structure of polystyrene, is C 6 H 5 C 2 H 5 , as shown in Figure 1. C 6 H 5 C 2 H 5 is decomposed into C 6 H 6 and CO via C 6 H 5 CH 2 , and C 6 H 5 C 2 H 3 , respectively, as shown in Figure 10a,b. The C 6 H 5 C 2 H 3 was the primary decomposition product of C 6 H 5 C 2 H 5 . As shown in Figure 10a,b, a significant amount of C 6 H 6 is generated during the course of the thermal decomposition of C 6 H 5 C 2 H 5 and C 6 H 5 CH 3 . This explains the delayed decomposition of C 6 H 6 shown in Figure 9a. The concentration of C 6 H 6 was nearly constant to the length of 10 because the decomposition rate of the fed C 6 H 6 is nearly equal to the formation rate of C 6 H 6 due to the decomposition of the fed hydrocarbons until the length of 10 cm. The steep increase in the CO 2 concentration during the course of the decomposition of the fed UHCs was due to the rapid increase in the generation of CO with the temperature according to the reaction pathway shown in Figure 10.
are depicted in Figure 10. The largest amount of UHC generated by the pyrolysis of CER, with the basic structure of polystyrene, is C6H5C2H5, as shown in Figure 1. C6H5C2H5 is decomposed into C6H6 and CO via C6H5CH2, and C6H5C2H3, respectively, as shown in Figure 10a,b. The C6H5C2H3 was the primary decomposition product of C6H5C2H5. As shown in Figure 10a,b, a significant amount of C6H6 is generated during the course of the thermal decomposition of C6H5C2H5 and C6H5CH3. This explains the delayed decomposition of C6H6 shown in Figure 9a. The concentration of C6H6 was nearly constant to the length of 10 because the decomposition rate of the fed C6H6 is nearly equal to the formation rate of C6H6 due to the decomposition of the fed hydrocarbons until the length of 10 cm. The steep increase in the CO2 concentration during the course of the decomposition of the fed UHCs was due to the rapid increase in the generation of CO with the temperature according to the reaction pathway shown in Figure 10. Figure 10. Reaction pathways of C6H5CH3 (a) and C6H5C2H5 (b) into C6H6, and that of C6H6 (c) into CO2. Figure 10. Reaction pathways of C 6 H 5 CH 3 (a) and C 6 H 5 C 2 H 5 (b) into C 6 H 6 , and that of C 6 H 6 (c) into CO 2 .
The concentrations of the fed UHCs at φ value of 0.5 and reactor temperature of 750 • C as a function of the reactor distance are shown in Figure 11a. The critical point of the reactor length is approximately 30 cm for the substantial destruction of the fed UHCs under this condition. Figure 11b shows that the aromatic hydrocarbons generated are also substantially decomposed at the reactor length just before 30 cm. However, 3000 ppm of carbon monoxide (CO) remaining after the reactor length of 16 cm is not further oxidized to 40 cm at a φ value of 0.5. The carbon monoxide (CO) cannot be substantially oxidized at a φ value of 0.5 and at 750 • C regardless of the reactor length (residence time). The concentrations of the fed UHCs at ϕ value of 0.5 and reactor temperature of 750 °C as a function of the reactor distance are shown in Figure 11a. The critical point of the reactor length is approximately 30 cm for the substantial destruction of the fed UHCs under this condition. Figure 11b shows that the aromatic hydrocarbons generated are also substantially decomposed at the reactor length just before 30 cm. However, 3000 ppm of carbon monoxide (CO) remaining after the reactor length of 16 cm is not further oxidized to 40 cm at a ϕ value of 0.5. The carbon monoxide (CO) cannot be substantially oxidized at a ϕ value of 0.5 and at 750 °C regardless of the reactor length (residence time). The UHC concentration when ϕ = 0.5 as a function of the PFR length and PFR temperature is plotted in Figure 12a. This 3-D contour plot shows a wide range of UHC combustor operating conditions for the substantial destruction of UHCs. As an example, UHCs are completely decomposed at a temperature of ≥800 °C and PFR length of 10 cm. However, the most critical parameter is the air equivalence ratio, which significantly influences the emission of CO, as shown in Figure 12b,c. In order to lower the emission concentration of CO to a level below the emission standard (100 ppm), ϕ = ≤0.35 is required at 800 °C. The design and operating parameters of the PFR-type UHC combustor were determined as follows: A PFR length of 10 cm (ID = 5 cm), a heating temperature of 800 °C, and a ϕ value of 0.3. The determined appropriate condition will result in the substantial destruction of UHCs and the oxidation of PICs without excess installation and operating costs. The UHC concentration when φ = 0.5 as a function of the PFR length and PFR temperature is plotted in Figure 12a. This 3-D contour plot shows a wide range of UHC combustor operating conditions for the substantial destruction of UHCs. As an example, UHCs are completely decomposed at a temperature of ≥800 • C and PFR length of 10 cm. However, the most critical parameter is the air equivalence ratio, which significantly influences the emission of CO, as shown in Figure 12b,c. In order to lower the emission concentration of CO to a level below the emission standard (100 ppm), φ = ≤0.35 is required at 800 • C. The design and operating parameters of the PFR-type UHC combustor were determined as follows: A PFR length of 10 cm (ID = 5 cm), a heating temperature of 800 • C, and a φ value of 0.3. The determined appropriate condition will result in the substantial destruction of UHCs and the oxidation of PICs without excess installation and operating costs.
The UHC concentration when ϕ = 0.5 as a function of the PFR length and PFR temperature is plotted in Figure 12a. This 3-D contour plot shows a wide range of UHC combustor operating conditions for the substantial destruction of UHCs. As an example, UHCs are completely decomposed at a temperature of ≥800 °C and PFR length of 10 cm. However, the most critical parameter is the air equivalence ratio, which significantly influences the emission of CO, as shown in Figure 12b,c. In order to lower the emission concentration of CO to a level below the emission standard (100 ppm), ϕ = ≤0.35 is required at 800 °C. The design and operating parameters of the PFR-type UHC combustor were determined as follows: A PFR length of 10 cm (ID = 5 cm), a heating temperature of 800 °C, and a ϕ value of 0.3. The determined appropriate condition will result in the substantial destruction of UHCs and the oxidation of PICs without excess installation and operating costs.

Determination of the Appropriate Halogenation Condition
The halogenation treatment condition was thermodynamically modelled to determine the ranges of reactor operating temperatures and the feed halogen gas concentration, which is also required for a detailed design and the selection of reactor materials. The mechanism of the vaporization of the elements is the distribution of the elements as a result of chemical reactions within the thermal treatment system. The exact distribution requires knowledge of all constituents, of all the possible reactions, and the reaction rate constants, as conducted for the determination of operating condition for the UHC combustor in this study. Accurate comprehension of the chemical reaction rate data is not available for inorganic elements with gases at high temperatures. In the absence of reaction rate data, it is often assumed that all reactions achieve chemical equilibrium in a relatively short period of time when compared to the total residence time of the reactants [22]. This is a possible approach to the problem, as numerous chemical reactions take place in the system despite the fact that all of the reaction data are not available [23].
The equilibrium model analysis in this study is based on the following assumptions: (1) Thermodynamic equilibrium is maintained in the halogenation reactor, and (2) all of the radioactive species present in the carbonized resins or gas-phase elements in the reactor are intimately mixed. If a given mixture of species undergoes a change that minimizes the total Gibbs free energy, this represents an equilibrium state and corresponds to the complete conversion of the reactants to products. The Gibbs energy function of a system is expressed as where g k is the partial molar Gibbs energy function and N k is the number of moles of each species k in the system; K is the total number of species. For ideal-gas mixtures or ideal solutions, the partial molar Gibbs function is given by where g k (T, P) is the Gibbs function for the pure species k evaluated at the system temperature and pressure, R is the universal gas constant, and X k is the mole fraction of the kth species. The equilibrium solution at a given temperature and pressure is the distribution of N k that minimizes the system Gibbs energy function G subject to atomic population constraints (and a non-negative N k ). The atomic population constraints are as follows: Here, n jk is the number of the jth atoms that appear in the kth molecule, P j denotes the total population in moles of the jth atom in the system, and M is the total number of different elements present in the system. HSC-Chemistry 7.1 software was used for the model calculation [24]. The simulated compositions of the carbonized spent CER and chlorination gas are shown in Table 1. The simulated mixing ratio of the condensed phase material (carbonized resin) to the chlorination gas was unity. The calculated results for the equilibrium mole fractions of the nonradioactive compounds and radioactive compounds are shown in Figure 13a,b respectively. Carbon, the major component of carbonized CER, plays an important role in the conversion of inorganic elements into volatile chlorides. As shown in Table 1, inorganic elements exist in the form of their respective sulfides, which are relatively stable at high temperatures. Figure 13a shows the increased mole fractions of S(g) and CO(g). This indicates that metal sulfides are readily reduced and chlorinated in the presence of carbon and chlorine. The following reaction, expressed by Equations (9) and (10), shows the significant role of carbon during the volatilization of metals in the form of nonvolatile sulfate. Calcium sulfate (CaSO 4 ) is a non-volatile compound at approximately ≤1500 • C. As an example, as shown in Equation (9), CaSO 4 is not converted into its volatile chloride (CaCl 2 ) in the presence of chlorine at 1400 • C. However, in the presence of carbon, CaSO 4 is readily converted into its volatile chloride (CaCl 2 ), even at a much lower temperature of 1000 • C. CaSO 4 + Cl 2 (g) = CaCl 2 (g) + SO 2 (g) + O 2 (g) ∆G = +10.9 kJ/mole at 1400 • C CaSO 4 + Cl 2 (g) + 2C = CaCl 2 (g) + S(g) + 4CO(g) ∆G = -329.7 kJ/mole at 1000 • C (10) chlorine at 1400 °C. However, in the presence of carbon, CaSO4 is readily converted into its volatile chloride (CaCl2), even at a much lower temperature of 1000 °C.
CaSO4 + Cl2(g) = CaCl2(g) + SO2(g) + O2(g) ΔG = +10.9 kJ/mole at 1400 °C (9) CaSO4 + Cl2(g) + 2C = CaCl2(g) + S(g) + 4CO(g) ΔG = -329.7 kJ/mole at 1000 °C (10) (a) (b)  Figure 13b shows the thermodynamically stable forms of the radioactive elements and their respective volatile chlorides at a temperature of ≥1130 °C. If we continuously flow chlorine gas through the bed of the carbonized resin granules at ≥1200 °C, we can readily remove metallic and radioactive elements from the granules.  Figure 13b shows the thermodynamically stable forms of the radioactive elements and their respective volatile chlorides at a temperature of ≥1130 • C. If we continuously flow chlorine gas through the bed of the carbonized resin granules at ≥1200 • C, we can readily remove metallic and radioactive elements from the granules.

Process Description
The thermochemical decontamination process is a two-stage process of carbonization and halogenation. Figure 14 shows the arrangement of unit for the proposed thermochemical processes. The key units are a carbonization/halogenation reactor, the UHCs (unburned hydrocarbons), a combustor, and a wet acid gas scrubber. The detailed designs of the carbonization/halogenation reactor and PFR-type UHC combustor were created based on the results of a numerical modeling study. During the first stage of the treatment, the pyrolysis and carbonization of the spent CER, significant amounts of H 2 O, SO 2 , and UHCs are generated. To prevent the oxidation loss of graphite materials in the multifunctional reactor, a vacuum condition is maintained without supplying nitrogen during the course of carbonization. The complete sealing of the multifunctional reactor and the installation of a vacuum pumping system, as shown in Figure 14, were required for this purpose.

Process Description
The thermochemical decontamination process is a two-stage process of carbonization and halogenation. Figure 14 shows the arrangement of unit for the proposed thermochemical processes. The key units are a carbonization/halogenation reactor, the UHCs (unburned hydrocarbons), a combustor, and a wet acid gas scrubber. The detailed designs of the carbonization/halogenation reactor and PFR-type UHC combustor were created based on the results of a numerical modeling study. During the first stage of the treatment, the pyrolysis and carbonization of the spent CER, significant amounts of H2O, SO2, and UHCs are generated. To prevent the oxidation loss of graphite materials in the multifunctional reactor, a vacuum condition is maintained without supplying nitrogen during the course of carbonization. The complete sealing of the multifunctional reactor and the installation of a vacuum pumping system, as shown in Figure 14, were required for this purpose. UHCs are treated by the PFR-type combustor with a 5 cm ID and a 20 cm L with a supply of combustion air of ϕ = 0.3 according to the determined a condition. SO2 is collected in a conventional wet scrubber with an alkaline (NaOH) solution. During the second stage of the treatment, halogenation of pyrocarbon bearing radionuclides at a higher UHCs are treated by the PFR-type combustor with a 5 cm ID and a 20 cm L with a supply of combustion air of φ = 0.3 according to the determined a condition. SO 2 is collected in a conventional wet scrubber with an alkaline (NaOH) solution. During the second stage of the treatment, halogenation of pyrocarbon bearing radionuclides at a higher temperature generates vapors of metal/radionuclide halides. The vapors of these metallic species then condense into particulates as the off-gas cools. This is done by passing them through the wet scrubber, which is operated under atmospheric temperatures. Some portion of the particulates is collected in the wet scrubber and the remainder is collected in the HEPA filter with a collection efficiency of ≥99.97% for 0.3 µm particles. In this manner, the generated flue gas bearing hazardous constituents with the acid gas (SO 2 ), UHCs, and vapors of hazardous/radioactive metal species are substantially collected at a level below the emission standards.
Two important advantages of the proposed process are the smaller plant size and the lower volume of the final radwaste requiring disposal. The generated volume of off-gas is much smaller because most of the carbon species in the CER are not gasified or combusted. This results in a smaller plant size when compared to that of a conventional radwaste incineration plant. In the proposed process, only inorganic elements are vaporized and collected as secondary radioactive waste. No carbon-bearing fly-ash due to the turbulence of combustion gas is generated during the proposed thermochemical process. Therefore, no primary filtering system, such as a bag-filter system, is required. These advantages result in a much smaller volume of secondary waste as well as a much smaller size of the off-gas treatment system.

Detailed Design of the Multifunctional Reactor and Test Results
The detailed design of the multifunctional reactor for the carbonization of the CER, images of the inside of the reactor after the feeding of the CER and after the treatment, and the results of the SEM-EDS (Scanning Electron Microscope-Energy Dispersive X-ray Spectrometer) analysis of the carbonized CER and the chlorination-treated carbonized CER are shown in Figure 15. As shown in Figure 15a, all reactor components are made of graphite, as graphite is the only material available that can endure halogen gases at very high temperatures. The processing materials, spent CERs, are spherical granules with diameters 0.3~0.8 cm in size. Therefore, a type of vertical packed-bed reactor, through which a carrier gas or a reacting gas flows up, is used as a multifunctional reactor. This multifunctional reactor conducts two different reacting processes in a stepwise manner.
Basic performance tests using CER doped with nonradioactive Co and Cs with an initial mass content of 0.1% of each metal were conducted under the determined appropriate carbonization and halogenation treatment conditions. Simulated spent CERs doped with nonradioactive Co and Cs were loaded into the packed-bed reactor. The reactor was then heated to 800 • C and this temperature was sustained for 40 min under a N 2 flowing condition according to the appropriate carbonization temperature and time profile shown in Figure 6. After this carbonization step was complete, the temperature of the reactor was raised further to 1500 • C by flowing Cl 2 and this stage was sustained for one hour. The results of a SEM-EDX analysis of carbonized CER and halogenation-treated carbonized CER shown in Figure 15d,e present the substantial removal of surrogate metals in the spent CER, Co, and Cs, by the applied carbonization and halogenation treatment. The results of these tests demonstrate that the noble thermochemical process proposed in this study is a viable process that effectively removes radioactive elements from spent CER. The required processing time for the halogenation treatment for the substantial removal of all radionuclides from spent CER to reduce their concentrations to levels below the free-release criteria will be determined by demonstration treatment of actual radioactive spent CER. Spectrometer) analysis of the carbonized CER and the chlorination-treated carbonized CER are shown in Figure 15. As shown in Figure 15a, all reactor components are made of graphite, as graphite is the only material available that can endure halogen gases at very high temperatures. The processing materials, spent CERs, are spherical granules with diameters 0.3~0.8 cm in size. Therefore, a type of vertical packed-bed reactor, through which a carrier gas or a reacting gas flows up, is used as a multifunctional reactor. This multifunctional reactor conducts two different reacting processes in a stepwise manner. Basic performance tests using CER doped with nonradioactive Co and Cs with an initial mass content of 0.1% of each metal were conducted under the determined appropriate carbonization and halogenation treatment conditions. Simulated spent CERs doped with nonradioactive Co and Cs were loaded into the packed-bed reactor. The reactor was then heated to 800 °C and this temperature was sustained for 40 min under a N2 flowing condition according to the appropriate carbonization temperature and time profile shown in Figure 6. After this carbonization step was complete, the temperature of the reactor was raised further to 1500 °C by flowing Cl2 and this stage was sustained for one hour. The results of a SEM-EDX analysis of carbonized CER and halogenation-treated carbonized CER shown in Figure 15d,e present the substantial removal of surrogate metals in the spent CER, Co, and Cs, by the applied carbonization and halogenation treatment. The results of these tests demonstrate that the noble thermochemical process proposed in this study is a viable process that effectively removes radioactive elements from spent CER. The required processing time for the halogenation treatment for the substantial removal of all radionuclides from spent CER to reduce their concentrations to levels below the freerelease criteria will be determined by demonstration treatment of actual radioactive spent CER.

Conclusions
A novel thermochemical process for the removal of radionuclides from spent cationexchange resins was proposed in this study. A step-by-step experimental and numerical modeling study was conducted for the design and establishment of the proper operation conditions for the carbonization and halogenation reactor and the UHC combustor. Based on the results of experimental and modeling study, an integrated process consisting of a multifunctional reactor made of graphite, which can safely conduct the halogenation treatment at a very high temperature, was realized. The optimum operating conditions could be established based on the results of a thermal analysis of the CER, a nonisothermal kinetic analysis, a numerical modeling study of a PFR-type combustor, and a thermodynamic equilibrium composition analysis. The results of this study present detailed design of a novel multifunctional reactor and operating conditions of a bench-scale carbonization and halogenation process. The results of basic performance tests using nonradioactive surrogates showed that the thermochemical process proposed here is an executable process that effectively removes radioactive elements from spent CER.