U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Recovery of cesium

Patent 4477377 Issued on October 16, 1984. Estimated Expiration Date: Icon_subject June 17, 2002. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

System for disposing of radioactive waste
Patent #: 4196169
Issued on: 04/01/1980
Inventor: Gablin ,   et al.

Conversion of radioactive waste materials into solid form
Patent #: 4230597
Issued on: 10/28/1980
Inventor: Bustard ,   et al.

Rhodium recovery process Patent #: 4363765
Issued on: 12/14/1982
Inventor: Fiato ,   et al.

Inventors

Assignee

Application

No. 06/389402 filed on 06/17/1982

US Classes:

423/181, Ion exchanging or liquid-liquid extracting210/643, Utilizing liquid membrane (e.g., emulsion) in liquid/liquid solvent or colloidal extraction210/650, Filtering through membrane (e.g., ultrafiltration)210/651, Removing specified material252/634In form of sol solution or gel

Examiners

Primary: Hunt, Brooks H.
Assistant: Locker, Howard J.

International Class

G21F 9/00 (20060101)

Abstract

A process of recovering cesium ions from mixtures of ions containing them and other ions, e.g., a solution of nuclear waste materials, which comprises establishing a separate source phase containing such a mixture of ions, establishing a separate recipient phase, establishing a liquid membrane phase in interfacial contact with said source and recipient phases, said membrane phase containing a ligand, preferably a selected calixarene as depicted in the drawing, maintaining said interfacial contact for a period of time long enough to transport by said ligand a substantial portion of the cesium ion from the source phase to the recipient phase, and recovering the cesium ion from the recipient phase. The separation of the source and recipient phases may be by the membrane phase only, e.g., where these aqueous phases are emulsified as dispersed phases in a continuous membrane phase, or may include a physical barrier as well, e.g., an open-top outer container with an inner open-ended container of smaller cross-section mounted in the outer container with its open bottom end spaced from and above the closed bottom of the outer container so that the membrane phase may fill the outer container to a level above the bottom of the inner container and have floating on its upper surface a source phase and a recipient phase separated by the wall of the inner container as a physical barrier. A preferred solvent for the ligand is a mixture of methylene chloride and carbon tetrachloride.

Other References

  • Jacobs, D., 1962, Cesium Exchange Properties of Vermiculite, Nuclear Science and Engineering, 12:285-292
  • A. Zinke & E. Ziegler, Zur Kenninis des Hartungsporzesses, vol. 77, 1944, pp. 264-273, Chem. Ber
  • J. D. Lamb, R. M. Izatt, J. J. Christensen, D. J. Eatough, Coordination Chemistry of Macrocyclic Compounds, ed. by G. A. Melson, Plenum, 1979
  • C. D. Gutsche, R. Muthukrishnan, Calixarenes. 1. Analysis of the Product Mixtures Produced by the Base-Catalyzed Condensation of Formaldehyde with Para-Substituted Phenols, 1978, pp. 4905-4906, J. Org. Chem., vol. 43
  • H. Kammerer & G. Happel, Stufenweise Darstellung Eines Cycloheptamers aus p-Kresol, 4-tert-Butylphenol und Formaldehyd. Vergleich mit Einem Phenolischen, Heptanuklearen Kettenoligomer, 1980, pp. 2049-2062, Makromol. Chem., vol. 181
  • A. Ninagwa & H. Matsuda, Isolation and Characterization of Calix[5]Arene from the Condensation Product of 4-tert-Butylpheol with Formaldehyde, 1982, pp. 65-67, Makromol. Chem. Rap. Comm., vol. 3
  • C. D. Gutsche, B. Dhawan, K. H. No, & R. Muthukrishnan, Calixarenes 4. The Synthesis, Characterization, and Properties of the Calixarenes from P-tert-Butylphenol., 1981, pp. 3782-3792, J. Am. Chem. Soc., vol. 103
  • E. M. Choy, D. F. Evans, E. L. Cussler, A Selective Membrane for Transporting Sodium Ion Against Its Concentration Gradient, 1974, pp. 7085-7090, J. Am. Chem. Soc., vol. 96
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