Ion Exchange Characteristics of Palladium and Ruthenium from a Simulated Radioactive Liquid Waste

2003 ◽  
Vol 38 (14) ◽  
pp. 3459-3472 ◽  
Author(s):  
S. H. Lee ◽  
H. Chung
2021 ◽  
pp. 871-877
Author(s):  
Aamir Abdullah Mohammed ◽  
Hayder S. Hussain ◽  
Salam K. Al-Nasri

Radioactive liquid waste contaminated with cesium-137 found in the radiochemistry laboratories at Tuwaitha site, south of Baghdad, was treated in this work. Bentonite was used as a sorbent material for the removal of radioactive cesium-137 from liquid waste by ion exchange method. The results indicated that the best removal efficiency obtained was 95.13% with experimental conditions of 2 h mixture time, 0.04 g sorbent mass, and pH=10 for the radioactive liquid. It was found that the experimental results match well with Langmuir and Freundlich models, with better matching with the latter.


Author(s):  
Pinky Septria Adella ◽  
Asih Wijayanti ◽  
Dwi Indrawati ◽  
Sugeng Purnomo

Radioactive liquid waste is a hazardous and toxic waste which comes from nuclear research laboratory. This waste may cause explosion when treated with evaporator. <strong>Aim:</strong> This research was intended to reduce and determine the best removal method of Cs-137 and Co-60 from radioactive liquid waste. <strong>Methodology and Result</strong>: Methods used in this research are ion exchange and coagulation-flocculation method. In ion exchange method used two types of reactor that is continuous reactor and batch reactor with variables of debit, material type, mesh size and mass of material, while in coagulation-flocculation method used jar test with ferro sulfate coagulant dose variables. Continuous reactor consisting of separating funnel and chromatography column with a diameter of 4 cm and height 60 cm, whereas in batch reactor used jar test stirrer. The application of radioactive liquid waste treatment is done using selected method, with the start condition for Cs-137 of 3 x 10-5 mCi/L and for Co-60 of 4.8 x 10-6 mCi/L. Application of Ion Exchanger with Continuous Reactor Speed 60 mL/10 sec and Coagulation-Flocculation with dose of 100 mmol/L in pH 8 effluent result the value for Cs-137 and Co-60 that undetected or very little, below 10-6 mCi/L. <strong>Conclusion, significance and impact study:</strong> The conclusion of this study is suitable with the Government Regulation Number 10 of 1997 about nuclear power, the limit of quality standard for Cs-137 and Co-60 is below 10-6 mCi/L. So the appropriate method to treat of Cs-137 and Co-60 are Ion Exchanger with Continuous Reactor Speed 60 mL/10 sec and Coagulation-Flocculation with dose of 100 mmol/L in pH 8.


2003 ◽  
Vol 792 ◽  
Author(s):  
V. Aubin ◽  
D. Caurant ◽  
D. Gourier ◽  
N. Baffier ◽  
S. Esnouf ◽  
...  

ABSTRACTProgress on separating the long-lived fission products from the high level radioactive liquid waste (HLW) has led to the development of specific host matrices, notably for the immobilization of cesium. Hollandite (nominally BaAl2Ti6O16), one of the main phases constituting Synroc, receives renewed interest as specific Cs-host wasteform. The radioactive cesium isotopes consist of short-lived Cs and Cs of high activities and Cs with long lifetime, all decaying according to Cs+→Ba2++e- (β) + γ. Therefore, Cs-host forms must be both heat and (β,γ)-radiation resistant. The purpose of this study is to estimate the stability of single phase hollandite under external β and γ radiation, simulating the decay of Cs. A hollandite ceramic of simple composition (Ba1.16Al2.32Ti5.68O16) was essentially irradiated by 1 and 2.5 MeV electrons with different fluences to simulate the β particles emitted by cesium. The generation of point defects was then followed by Electron Paramagnetic Resonance (EPR). All these electron irradiations generated defects of the same nature (oxygen centers and Ti3+ ions) but in different proportions varying with electron energy and fluence. The annealing of irradiated samples lead to the disappearance of the latter defects but gave rise to two other types of defects (aggregates of light elements and titanyl ions). It is necessary to heat at relatively high temperature (T=800°C) to recover an EPR spectrum similar to that of the pristine material. The stability of hollandite phase under radioactive cesium irradiation during the waste storage is discussed.


2002 ◽  
Vol 90 (3) ◽  
Author(s):  
Y. Sugo ◽  
Y. Sasaki ◽  
S. Tachimori

SummaryHydrolytic and radiolytic stabilities of a promising extractant, N,N,N′,N′-tetraoctyl-3-oxapentane-1,5-diamide (TODGA), for actinides in high-level radioactive liquid waste from nuclear fuel reprocessing were investigated in air at room temperature. Hydrolysis by nitric acid was not observed, whereas radiolysis by gamma irradiation was notably observed. The radiolysis study showed that an amide-bond, an ether-bond, and a bond adjacent to the ether-bond tended to be broken by gamma irradiation, and dioctylamine and various N,N-dioctylmonoamides were identified as the main degradation products by GC/MS and NMR analyses. The


Sign in / Sign up

Export Citation Format

Share Document