Advanced ORIENT Cycle: Progress on Fission Product Separation and Utilization

Author(s):  
Isao Yamagishi ◽  
Masaki Ozawa ◽  
Hitoshi Mimura ◽  
Shohei Kanamura ◽  
Koji Mizuguchi

Fission reaction of U-235 and/or plutonium generates more than 40 elements and 400 nuclides in the spent fuel. Among them, 31 elements are categorized as rare metals. In a conventional fuel cycle U and Pu are reused but others are vitrified for disposal. Adv.-ORIENT (Advanced Optimization by Recycling Instructive Elements) Cycle strategy was drawn up for the minimization of radio-toxicity and volume of radioactive waste as well as the utilization of valuable elements/nuclides in the waste. The present paper describes the progress on Fission Products (FP) separation in this Cycle. Highly functional inorganic adsorbent (AMP-SG, silica gel loaded with ammonium molybdophosphate) and organic microcapsule (CE-ALG, alginate gel polymer enclosed with crown ether D18C6) were developed for separation of heat-generating Cs and Sr nuclides, respectively. The AMP-SG adsorbed more than 99% of Cs selectively from a simulated High-level Liquid Waste (HLLW). The ALG microcapsule adsorbed 0.0249 mmol/g of Sr and exhibited the order of its selectivity; Ba > Sr > Pd >> Ru > Rb > Ag. The electrodeposition is advantageous for both recovery and utilization of PGMs (Ru, Rh, Pd) and Tc because PGMs are recovered as metal on Pt electrode. Among PGMs, Pd was easily deposited on the Pt electrode. In the presence of Pd or Rh the reduction of Ru and Tc was accelerated more in hydrochloric acid media than in nitric acid. In the simulated HLLW, the redox reaction of Fe(III)/Fe(II) disturbed deposition of elements except for Pd. The deposits on Pt electrode showed higher catalytic reactivity on electrolytic hydrogen production than the original Pt electrode. The reactivity of deposits prepared from the simulated HLLW was higher than that from solution containing only PGM.

2012 ◽  
Vol 560-561 ◽  
pp. 637-643
Author(s):  
Yong Li ◽  
Xue Gang Liu ◽  
Jin Chen

The proper management of spent fuel arising from nuclear power production is a key issue for the sustainable development of nuclear energy. While conventional reprocessing process, PUREX process, was successful to recover uranium and plutonium, in recent years some countries have turned to focus on advanced reprocessing process, which features of partitioning of minor actinides (MA) and long-lived fission products(LLFP). Most advanced reprocessing processes under development involve new extractants and additional extraction cycles. In China, TRPO extraction process has been developed to partition MA/LLFP from high-level liquid waste(HLLW) since early 1980’s. In parallel to R&D work on separation technologies, studies on concentration & denitration process have been evolved to prepare feed solutions to suit qualifications of extraction. Industrially, concentration & denitration is the internationally recognized standard to treat HLLW released from PUREX before vitrification. It enables to minimize the volume of interim storage, to restrain the corrosion of storage tank, to recover nitric acid in HLLW and to reduce the required evaporation duty of the vitrification process. Generally, the constitution of concentrated HLLW has little impact on the following vitrification process. But when concentration & denitration acts as pretreatment process of partitioning, the composition of actinides, fission products, and nitric acid in concentrated HLLW solution plays significant role in extraction process. A series of technical issues relevant to the connection between concentration ﹠denitration and extractions should be solved. This paper describes current status of concentration & denitration technology utilized in industry and under reprocessing plants. The specific separation requirements in advanced reprocessing process and challenges to apply concentration & denitration process are addressed. Besides, concentration & denitration process was tested in laboratory to adjust feed solutions for TRPO and Cyanex301 partitioning. Results demonstrate its promising prospect in advanced reprocessing process.


1987 ◽  
Vol 112 ◽  
Author(s):  
B. Grambow ◽  
D. M. Strachan

The reprocessing of spent fuel from nuclear reactors and processing of fuels for defense purposes have generated large volumes of high-level liquid waste that need to be immobilized prior to final storage. For immobilization, the wastes must be converted to a less soluble solid, and, although other waste forms exist, glass currently appears to be the choice for the transuranic-containing portion of the reprocessed waste. Once produced, this glass will be sent in canisters to a geologic repository located some 200 to 500 m below the surface of the earth.


Estimates are given of the total quantities of radioactivity, and of the contribution from different isotopes to this total, arising in the wastes from civil nuclear power generation; the figures are normalized to 1 GW (e) y of power production. The intensity of the heat and y-radiation emitted by the spent fuel has been calculated, and their decrease as the radioactivity decays. Reprocessing the spent fuel results in 95% or more of the fission products and higher actinides being concentrated in a small volume of high-level, heat-emitting waste. The total decay curve of unreprocessed spent fuel or of the separated high-level waste is dominated by the decay of some fission products for a few hundred years and then by the decay of some actinide isotopes for some tens of thousands of years. The residual activity is compared with that of the original uranium ore. Some of the long-lived activity will appear in other waste streams, particularly on the fuel cladding, and the volumes and activities of these wastes arising in this country are recorded. The long-lived activity arising from reactor decommissioning will be small compared with the annual arisings from the fuel cycle.


1989 ◽  
Vol 176 ◽  
Author(s):  
Hiroshi Igarashi ◽  
Takeshi Takahashi

ABSTRACTWaste forms have been developed and characterized at PNC (Power Reactor and Nuclear Fuel Development Corporation)to immobilize high-level liquid waste generated from the reprocessing of nuclear spent fuel.Mechanical strength tests were excecuted on simulated solidified highlevel waste forms which were borosilicate glass and diopside glass-ceramic. Commercial glass was tested for comparison. Measured strengths were three-point bending strength,uniaxial compressive strength,impact strength by falling weight method,and Vickers hardness. Fracture toughness and fracture surface energy were also measured by both notch-beam and indentation technique.The results show that mechanical strengths of waste glass form are similar and that the glass ceramic form has the higher fracture toughness.


Author(s):  
Namitha J. ◽  
Ujjwal Kumar Maity ◽  
G. G. S. Subramanian ◽  
Manoravi Periasamy ◽  
Joseph M ◽  
...  

In any nuclear industry which follows a closed nuclear fuel cycle, determination of 90Sr and 137Cs present in high level liquid waste (HLLW) is of major concern because of its...


2012 ◽  
Vol 482-484 ◽  
pp. 58-61 ◽  
Author(s):  
Ming Fen Wen ◽  
Bo Yu ◽  
Min Luo ◽  
Jing Chen

The presence of long-lived radionuclides is a challenge to the management of high level liquid waste (HLLW). Separation of minor acitinides and long-lived fission products from the HLLW by partitioning process has the potential of significantly decreasing the costs of the immobilization and disposal of the radioactive waste by minimizing waste volumes. Several solvent extraction processes have been developed and demonstrated at the Institute of Nuclear and New Energy Technology (INET) for the separation of transuranic elements, 90Sr and 137Cs. In this work, using modified zeolite molecular sieve as a sorbent carrier, four kinds of solidification were prepared by soakage- absorption- calcination methods. It was found that the sample (HZCS-75) calcinated at 750°C was formed pollucite, a zeolite mineral, which will provide an option to immobilize the radioactive cesium and strontium.


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