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author:

Wang, J. H. (Wang, J. H..) [1] | Li, Q. (Li, Q..) [2] | Wu, M. H. (Wu, M. H..) [3] (Scholars:吴明红) | Xu, G. (Xu, G..) [4] | Li, Ch (Li, Ch.) [5] | Bao, B. R. (Bao, B. R..) [6] | Zheng, W. F. (Zheng, W. F..) [7] | He, H. (He, H..) [8] | Zhang, Sh D. (Zhang, Sh D..) [9]

Indexed by:

SCIE

Abstract:

N,N-dimethylhydroxylamine (DMHA) is a novel salt-free reducing reagent used in the separation U from Pu and Np in the reprocessing of power spent fuel. This paper reports on the radiolysis of aqueous DMHA solution and its radiolytic liquid organics. Results show that the main organics in irradiated DMHA solution are N-methyl hydroxylamine, formaldehyde and formic acid. The analysis of DMHA and N-methyl hydroxylamine were performed by gas chromatography, and that of formaldehyde was performed by ultraviolet-visible spectrophotometry. The analysis of formic acid was performed by ion chromatography. For 0.1-0.5 mol L-1 DMHA irradiated to 5-25 kGy, the residual DMHA concentration is (0.07-0.47) mol L-1, the degradation rate of DMHA at 25 kGy is 10.1-30.1%. The concentrations of N-methylhydroxylamine, formaldehyde and formic acid are (8.25-19.36) x 10(-3), (4.20-36.36) x 10(-3) and (1.35-10.9) x 10(-4) mol L-1, respectively. The residual DMHA concentration decreases with the increasing dose. The concentrations of N-methylhydroxylamine and formaldehyde increase with the dose and initial DMHA concentration, and that of formic acid increases with the dose, but the relationship between the concentration of formic acid and initial DMHA concentration is not obvious.

Keyword:

N,N-dimethyl hydroxylamine Organics Radiolysis Reprocessing Spent fuel

Community:

  • [ 1 ] [Wang, J. H.]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 2 ] [Li, Q.]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 3 ] [Wu, M. H.]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 4 ] [Xu, G.]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 5 ] [Li, Ch]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 6 ] [Bao, B. R.]Shanghai Univ, Shanghai Appl Radiat Inst, Sch Environm & Chem Engn, Shanghai 200444, Peoples R China
  • [ 7 ] [Zheng, W. F.]China Inst Atom Energy, Dept Radiochem, Beijing 102413, Peoples R China
  • [ 8 ] [He, H.]China Inst Atom Energy, Dept Radiochem, Beijing 102413, Peoples R China
  • [ 9 ] [Zhang, Sh D.]China Inst Atom Energy, Dept Radiochem, Beijing 102413, Peoples R China

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Source :

JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY

ISSN: 0236-5731

Year: 2012

Issue: 1

Volume: 292

Page: 249-254

1 . 4 6 7

JCR@2012

1 . 5 0 0

JCR@2023

JCR Journal Grade:1

CAS Journal Grade:2

Cited Count:

WoS CC Cited Count:

SCOPUS Cited Count: 6

ESI Highly Cited Papers on the List: 0 Unfold All

WanFang Cited Count:

Chinese Cited Count:

30 Days PV: 0

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