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Volume 20 Issue 2
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Article Navigation >  LASER TECHNOLOGY  > 1996 >  20(2): 88-91

Citation:
shu

Chemical reaction uraninm isotope seperation by CO laser activation

  • 1.

    Dept.of Modern Appl.Phys, Tsinghua Univ;

  • 2.

    National Lab.of Molecular Reaction Dynamics, Institute of Chemistry, Academia Sinica;

  • 3.

    Dept. of Chemistry, Tsinghua Univ.;

  • 4.

    Dept. of Engineering Phys., Tsinghua Univ.

  • Received Date: 1994-10-05
    Accepted Date: 1995-08-27
  • The feasibility of CRISLA methode is confirmed by the laser catalytic reaction of UF6 and HCl using the optimum CO laser spectrum of uranium isotope seperation which is selected from the 3ν3 optoacoustic aborption spectra of 235UF6 and 238UF6.
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  • [1]

    Ferkens J W. US Patrnt No.4082633, 1978,Apr. 4
    [2]

    Ferkens J W. Appl Phys. 1976;10(1):15
    [3]

    Ferkens J W. Australia Patent Abridgment, AU8-66607/81,1981
    [4]

    Ferkens J W.Gria R P et al. Conference on lasers and electro-optics,. Sen Fnsociaco. California. 1986 June
    [5] 衷庆华.张健.王盛伟et al.激光光与红外.1991;21(1):42
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  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

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Chemical reaction uraninm isotope seperation by CO laser activation

  • 1. Dept.of Modern Appl.Phys, Tsinghua Univ;
  • 2. National Lab.of Molecular Reaction Dynamics, Institute of Chemistry, Academia Sinica;
  • 3. Dept. of Chemistry, Tsinghua Univ.;
  • 4. Dept. of Engineering Phys., Tsinghua Univ.
  • Received Date: 1994-10-05
  • Accepted Date: 1995-08-27
  • Available Online: 1996-03-25

Abstract: The feasibility of CRISLA methode is confirmed by the laser catalytic reaction of UF6 and HCl using the optimum CO laser spectrum of uranium isotope seperation which is selected from the 3ν3 optoacoustic aborption spectra of 235UF6 and 238UF6.

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