ELECTROLYTIC TANK AND ELECTROLYTIC METHOD FOR HIGH-EFFICIENCY DRY REPROCESSING
20180202057 ยท 2018-07-19
Inventors
Cpc classification
G21C19/46
PHYSICS
C25C7/00
CHEMISTRY; METALLURGY
Y02E30/30
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
C25C3/34
CHEMISTRY; METALLURGY
G21C19/46
PHYSICS
Abstract
A molten salt electrolysis tank, comprises: an anode feeder which is equipped with a mechanism for recovering deteriorated contact resistance that takes place between the metal fuel rod and the anode in the course of the anodic electrolysis; a cathode feeder which is controlled so as to have a potential in a range that causes U and/or Pu ions to be reduced to metal; a heating mechanism for locally heating the metal fuel rod and/or an excitation mechanism for bringing the metal fuel rod into a locally excited state; and a solenoid coil or a permanent magnet that is disposed between the anode feeder and the cathode feeder so as to improve separation efficiency of U and/or Pu ions by applying a combination of an electric field and a magnetic field.
Claims
1. A molten salt electrolysis tank in which electrolytic refining is performed by dissolving a spent metal fuel pin through anodic electrolysis in a crucible filled with a molten salt to cause U and/or Pu to be reduced and precipitated once again on a surface of a cathode, the spent metal fuel pin containing elements including zirconium (Zr) and uranium (U), U and plutonium (Pu), or Zr and U and Pu, the electrolytic tank comprising: an anode feeder that is provided with a mechanism for recovering from deterioration of contact resistance between the metal fuel pin and the anode in a course of the anodic electrolysis; a cathode feeder that is connected to the cathode and controlled at a potential in a range that causes U and/or Pu ions to be reduced to metal; a heating mechanism for locally heating the metal fuel pin and/or an excitation mechanism for bringing the metal fuel pin to a locally excited state; and a solenoid coil or a permanent magnet that is disposed between the anode feeder and the cathode feeder to improve a separation efficiency of the U and/or Pu ions by applying a combination of an electric field and a magnetic field.
2. The electrolytic tank according to claim 1, further comprising a mechanism in which a leading end portion of the anode feeder is formed in a basket shape to receive the spent metal fuel pin, and a pressing plate for pressing the metal fuel pin is disposed inside the basket-shaped anode feeder, the mechanism allowing the pressing plate to be automatically pressurized and moved in a course of the anodic electrolysis, wherein recovery from deterioration of contact resistance between the metal fuel pin and the anode feeder is made by the mechanism.
3. The electrolytic tank according to claim 1, wherein a leading end portion of the anode feeder is formed in a basket shape to receive the spent metal fuel pin, a pressing plate for pressing the metal fuel pin is disposed inside the basket-shaped anode feeder, a mechanism that generates mechanical oscillation from 50 Hz to 200 kHz is further disposed at a junction portion between the basket-shaped anode feeder and the pressing plate, and recovery from deterioration of contact resistance between the metal fuel pin and the anode feeder is made by the mechanical oscillation of the pressing plate.
4. (canceled)
5. The electrolytic tank according claim 1, further comprising: a liquid metal Cd layer for reducing and adsorbing metal such as minor actinoid other than the anodically dissolved U, Pu at a lower portion of the anode feeder; and a Cd cathode feeder electrically connected to the liquid metal Cd layer.
6. (canceled)
7. The electrolytic tank according to claim 1, wherein a rotating device having a horizontal rotational shaft is provided externally of the crucible, the crucible is periodically swung around the rotational shaft to agitate the molten salt, and a molten salt on surfaces of the anode feeder and the cathode feeder are thereby separated and diffused.
8. The electrolytic tank according claim 1, further comprising: a pipe in the crucible for circulating the molten salt, and a filter and a circulation pump in the pipe, by which the molten salt is circulated and agitated, a molten salt on surfaces of the anode feeder and the cathode feeder are separated and diffused, and the molten salt is further purified.
9. The electrolytic tank according to claim 1, wherein a magnetic field is applied using the solenoid coil or the permanent magnet in a direction that forms an angle of 60 to 90 with respect to a direction of an electric field applied between the anode feeder and the cathode feeder, by which a separation efficiency of the U and/or Pu ions is improved.
10. The electrolytic tank according to claim 1, wherein a concentration of radioactive elements is reduced by applying a low-frequency electromagnetic field of 100 kHz-20 MHz to the spent metal fuel pin and radioactive metal ions.
11. The electrolytic tank according to claim 1, wherein full-wave rectified or half-wave rectified AC power supply is used as an electrolytic current of the anodic electrolysis, and -decay rate is accelerated by applying an electric field having an AC component of 10.sup.5-10.sup.7 V/cm to surface layers on the anode feeder and the cathode feeder.
12. The electrolytic tank according to claim 1, wherein the anode feeder and/or the cathode feeder are irradiated with a laser beam having an output of 10.sup.12 W/cm.sup.2 or higher as the excitation mechanism, and -decay rate and/or -decay rate are accelerated.
13. (canceled)
14. An electrolytic method in which electrolytic refining is performed by dissolving a spent metal fuel pin through anodic electrolysis in a crucible filled with a molten salt to cause U and/or Pu to be reduced and precipitated once again on a surface of a cathode, the spent metal fuel pin containing elements including zirconium (Zr) and uranium (U), U and plutonium (Pu), or Zr and U and Pu, the electrolytic method with an improved electrolytic refining efficiency, comprising: when the anodic electrolysis is performed, using an anode feeder that is provided with a mechanism for recovering from deterioration of contact resistance between the metal fuel pin and the anode in a course of the anodic electrolysis; controlling a cathode feeder connected to the cathode at a potential in a range that causes U and/or Pu ions to be reduced to metal; locally heating the metal fuel pin by a heating mechanism and/or bringing the metal fuel pin to a locally excited state by an excitation mechanism; and disposing a solenoid coil or a permanent magnet between the anode feeder and the cathode feeder to improve a separation efficiency of the U and/or Pu ions by applying a combination of an electric field and a magnetic field.
15. The electrolytic method according to claim 14, wherein a leading end portion of the anode feeder is formed in a basket shape to receive the spent metal fuel pin, a pressing plate for pressing the metal fuel pin is disposed inside the basket-shaped anode feeder, and recovery from deterioration of contact resistance between the metal fuel pin and the anode is made by automatically pressurizing and moving the pressing plate in a course of the anodic electrolysis.
16. The electrolytic method according to claim 14, wherein a leading end portion of the anode feeder is formed in a basket shape to receive the spent metal fuel pin, a pressing plate for pressing the metal fuel pin is disposed inside the basket-shaped anode feeder, a mechanism that generates mechanical oscillation from 50 Hz to 200 kHz is further disposed at a junction portion between the basket-shaped anode feeder and the pressing plate, and recovery from deterioration of contact resistance between the metal fuel pin and the anode feeder is made by the mechanical oscillation of the pressing plate.
17. (canceled)
18. The electrolytic method according to claim 14, wherein metal such as minor actinoid other than the anodically dissolved U and Pu is reduced and adsorbed by a liquid metal Cd layer that is disposed at a lower portion of the anode feeder and is electrically connected to a Cd cathode feeder.
19. (canceled)
20. The electrolytic method according to claim 14, wherein by a rotating device that is mounted externally of the crucible and has a horizontal rotational shaft, the crucible is periodically swung around the rotational shaft to agitate the molten salt, and a molten salt on surfaces of the anode feeder and the cathode feeder are thereby separated and diffused.
21. The electrolytic method according to claim 14, wherein the molten salt is circulated and agitated by a pipe provided to the crucible, and a filter and a circulation pump provided in the pipe, a molten salt on surfaces of the anode feeder and the cathode feeder are separated and diffused, and the molten salt is further purified.
22. The electrolytic method according to claim 14, wherein a metal ion separation efficiency is improved by applying a magnetic field using the solenoid coil or the permanent magnet in a direction that forms an angle of 60 to 90 with respect to a direction of an electric field applied between the anode feeder and the cathode feeder.
23. The electrolytic method according to claim 14, wherein a concentration of radioactive elements is reduced by applying a low-frequency electromagnetic field of 100 kHz-20 MHz to the spent metal fuel pin and radioactive metal ions.
24. The electrolytic method according to claim 14, wherein full-wave rectified or half-wave rectified AC power supply is used as an electrolytic current, and -decay rate is accelerated by applying an electric field having an AC component of 10.sup.5-10.sup.7 V/cm to surface layers on the anode feeder and the cathode feeder.
25. The electrolytic method according to claim 14, wherein -decay rate and/or -decay rate are accelerated by irradiating the anode feeder and/or the cathode feeder with a laser beam having an output of 10.sup.12 W/cm.sup.2 or higher as the excitation mechanism.
26. (canceled)
Description
BRIEF DESCRIPTION OF DRAWINGS
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DESCRIPTION OF EMBODIMENTS
[0062] The content and effect of the present invention and are described in the following embodiments.
Embodiment 1
[0063] First, a method of favorably maintaining a contact resistance between a basket-shaped anode and finely cut metal fuel rod pins is described. As illustrated in
[0064]
[0065] In contrast, when the contact between the metal fuel rods and the basket-shaped anode is maintained at a low level using a spring structure as illustrated in
Embodiment 2
[0066] As the result shows in
[0067] Another embodiment is illustrated in
[0068] Another embodiment is illustrated in
[0069] As another example of mechanical oscillation, application of ultrasonic vibration is effective. For instance, it is effective to irradiate with ultrasonic wave from 10 kHz to 200 kHz, having an output of 1 W/cm.sup.2 or higher. It is also possible to use mechanical oscillation from 50 Hz to 10 kHz other than the ultrasonic wave.
Embodiment 3
[0070] Another embodiment that can agitate the molten salt in the crucible is illustrated in
Embodiment 4
[0071] Next,
[0072] Like this, the temperature of the metal fuel pins is raised stepwise, and a change in the amount of anodic dissolution was measured. The result is illustrated in
[0073] In addition, as another embodiment, when the metal fuel pins are anodically dissolved as illustrated in
[0074] Furthermore, when the fuel pins as the anode are anodically dissolved, a potential difference of 1-2 V is applied to the dissolution surface of the fuel pins. For instance, in the case of water electrolysis, it is expected that most of the potential is applied to approximately 10 (NON PATENT LITERATURE 4). It is assumed that the electrolytic reaction of the present invention is similar to the above reaction mechanism. Also, K, Li, Cl are used in the dry reprocessing, and when the ions of these and the size of H.sub.2O are compared, as compared with the case of water electrolysis, the thickness of an electric double layer in a dry reprocessing tank is considered to be several times greater. Therefore, in the case of dry reprocessing, when it is assumed that the thickness of the electric double layer is of the order of several times greater in consideration of ion radius and the like, the intensity of the electric field is 10.sup.5-10.sup.7 V/cm.
Embodiment 5
[0075] In Embodiment 1 to 3, the method to separating U, Pu ions and metal ions other than these by controlling the potentials of two types of cathodes has been adopted. In addition to this method, a separation method utilizing a magnetic field is shown below (see PATENT LITERATURE 1). Specifically, as illustrated in
M/Z=e(Br).sup.2/2E(M: mass, Z: charge number of ion, e: electric charge of electron, Br: magnetic flux density, E: electric field)[MATH. 4]
H=n(H: central magnetic field of coil, n: number of turns of coil, 1: current)[MATH. 5]
As seen from the formula, the position of the cathodes 40, 41 at which metal ions arrive depends on the value of M/Z. By utilizing this phenomenon, the separation efficiency of electrolytic refining can be improved. Although the separation efficiency depends on the intensity of the magnetic field, the separation efficiency depends on the number of turns of the coil and the current based on the relationship of B=H (: magnetic permeability). For instance, when the number of turns is 100, and the current value is 50 A, the central magnetic field H of the coil is 0.25 T (Tesla). The present invention is directed to U and Pu ions, and comparison between the characteristics of ions indicates that the magnetic field necessary in the present invention is 0.01 T or greater. However, in order to achieve an effective efficiency, application of a magnetic field of 0.25 T or greater, which is 10 times greater, is desirable.
Embodiment 6
[0076] Another embodiment using a magnetic field is illustrated in
[0077] Alternatively, a magnetic field can be formed using a solenoid coil instead of the permanent magnet.
Embodiment 7
[0078] The decay of radioactive nuclides is broadly divided into -decay and -decay. In general, after -decay, excessive energy is released and y decay occurs. According to quantum theory, -decay has an allowed transition type and a forbidden transition type, and regarding the half-life of -decay, in the case of allowed transition type, the half-life is shortened, and in the case of forbidden transition type, the half-life is lengthened. The radioactivity of -decay with the long half-life is a major problem for which environmental measures are to be taken. Reiss has studied this problem quantum-theoretically, and reports that -decay half-life is shortened by introducing terms regarding allowed transition by utilizing perturbation theory for the Hamiltonian which indicates a decay process (NON PATENT LITERATURE 5). Specifically, it is reported that -decay half-life may be shortened by applying a strong electromagnetic field of 200 kHz to 4.4 MHz. Using the crucible of the present invention enables acceleration of -decay. In the crucible having the structure illustrated in
Embodiment 8
[0079] Another embodiment of the -decay acceleration method described in Embodiment 7 is shown next. As described in Embodiment 4, when electrolysis is performed, a strong electric field of 10.sup.5-10.sup.7 V/cm is applied to several 10 on reaction surface layers of electrodes. As described in Embodiment 7, in addition to simple DC energization at the time of electrolysis, consideration of using AC is meaningful from a viewpoint of acceleration of the decay rate. However, in AC electrolysis, oxidation-reduction reactions occur substantially at the same time, and this is not desirable in this regard. However, with full-wave rectified or half-wave rectified, application of an electromagnetic wave and electrolysis can be performed at the same time. In Embodiment 7, 200 kHz-4.4 MHz is effective, however, when an electric field is directly applied, it is reported that even with DC, a reduction effect on the concentration of radioactive elements of ceramic-like nuclear fuel including U or Pu may be observed at a high temperature. The reduction of the concentration of radioactive elements indicates or -decay rate acceleration phenomenon. In addition, there is also a method of utilizing a high voltage by using DC current or a low-frequency fluctuating current of 50, 60 Hz (NON PATENT LITERATURE 6). In general, application of a high voltage causes electric discharge, and thus voltage application has a limit. When a high voltage is applied, vacuum is set up in many cases. For instance, in this report, application of DC with 3000V or AC with 50-60 Hz in a vacuum is proposed. When a voltage is applied, if a high voltage is applied under a precondition of a macroscopic distance, a high voltage of 3000 V or higher is necessary. Considering an effect on atoms or nuclei physically, not mere voltage but electric field has a significance. In the case of electrolysis in a molten salt, the atoms, which form an electrode surface layer, are to be electrically discharged. However, in the case of electrolysis in water, there is a problem that an electric discharge of water molecules occurs first. In this embodiment, for instance, the electrolytic current in the molten salt is set to 0.41 A/cm.sup.2 or lower, and full-wave rectified current with a frequency of 50 Hz or higher is passed. In this case, an electric field is directly applied to the electrode surface layer, and as described in Embodiment 4, a high electric field of 10.sup.5-10.sup.7 V/cm is applied to the surface layer. Essentially, a low-frequency high electric field applied to the radioactive elements on the surface layer causes acceleration of the decay rate. The frequency of low-frequency electromagnetic field is set to 100 KHz-20 MHz, and an AC electromagnetic field is further applied so that the anode potential becomes in a range of 2 to 1 V (V: Ag/AgCl). Like this, low-frequency electrolysis is effective as a high electric field application method. As shown in this embodiment, when both local heating and -decay rate acceleration are objected, the frequency of low-frequency electromagnetic field is preferably expanded to 1 KHz-20 MHz.
Embodiment 9
[0080] Next, an embodiment of an improvement method for the separation efficiency utilizing a laser beam, and an acceleration method for -decay rate is described. The present embodiment is a crucible utilizing a laser beam, and is illustrated in
Embodiment 10
[0081] The crucible structure of another embodiment illustrated in
[0082] For the laser using the crucible structure in
[0083] It is reported that when the spent nuclear fuel pins in the present invention are electrolytically refined, in the process of dissolving the surface layer of the metal fuel pins placed in the basket-shaped anode, the surface layer is selectively and partially dissolved along a structure (such as a crystal grain boundary) of metal crystals (NON PATENT LITERATURE 8). This indicates that partially undissolved colloidal metal particulates may be released. Conversely, the entire surface of the cathode side is also selectively reduced and precipitated. These phenomena indicate that it is probable that metal colloidal unstable particulates are formed on the electrode surface layer. Microscopic observation of the metal texture shows clusters of crystal grains. Needless to say, many transitions exist inside the crystal grains. When metal is anodically dissolved, first, dissolution starts at a weak portion. The weak portion corresponds to a crystal grain boundary or a portion of transition. When a crystal grain boundary, a transition are selectively dissolved, the remaining crystal grains are more likely to come off. The dimension of crystal grains depends on a processing method, and is extensively distributed from nm order to 10 m. In the present invention, the fuel pins are injection molded, and thus growth of crystal grains is inhibited, and crystal grains on the order of m or less were observed (NON PATENT LITERATURE 9). When irradiation with a high-output laser beam is made as described above in a state where metal colloids are formed on the surfaces of the anode and the cathode, the effect of shortening -decay half-life can be expected.
[0084] Although the above description of the embodiments has been made, the present invention is not limited to the embodiments, and it is apparent to those skilled in the art that various changes and modifications may be made within a scope of the spirit of the present invention and the accompanying claims.
REFERENCE SIGNS LIST
[0085] 1 electrolytic tank [0086] 10 crucible [0087] 12 crucible cover [0088] 13 molten salt drain pipe [0089] 14 molten salt drain pipe valve [0090] 20 molten salt [0091] 21 molten salt circulation pipe [0092] 22 molten salt filter [0093] 23 circulation pump [0094] 30 anode feeder [0095] 31 basket-shaped anode [0096] 32 fuel pin pressing plate [0097] 33 fuel pin [0098] 35 hollow anode feeder [0099] 36 laser [0100] 37 transparent fuel pin pressing plate [0101] 39 mechanical oscillation mechanism [0102] 40 cathode feeder [0103] 41 cathode [0104] 42 solenoid coil [0105] 50 Cd cathode feeder [0106] 60 liquid Cd cathode tank [0107] 61 liquid Cd drain pipe [0108] 62 liquid Cd [0109] 63 liquid Cd drain pipe valve [0110] 70 rotational shaft [0111] 81 crucible induction heating coil [0112] 82 separation efficiency improvement solenoid coil [0113] 83 anode local induction heating coil [0114] 85 permanent magnet N pole [0115] 86 permanent magnet S pole [0116] 90 fuel pin pressing spring fixing case [0117] 91 fuel pin pressing spring