EP2101333A1 - Verfahren zur umverarbeitung von flüssigen radioaktiven abfallstoffen (und varianten) - Google Patents

Verfahren zur umverarbeitung von flüssigen radioaktiven abfallstoffen (und varianten) Download PDF

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Publication number
EP2101333A1
EP2101333A1 EP07852046A EP07852046A EP2101333A1 EP 2101333 A1 EP2101333 A1 EP 2101333A1 EP 07852046 A EP07852046 A EP 07852046A EP 07852046 A EP07852046 A EP 07852046A EP 2101333 A1 EP2101333 A1 EP 2101333A1
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EP
European Patent Office
Prior art keywords
synthesis
layer
radionuclides
particles
oxides
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Application number
EP07852046A
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English (en)
French (fr)
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EP2101333A4 (de
EP2101333B1 (de
Inventor
Valentin Alexandrovich Avramenko
Vitaly Georgievich Dobrzhansky
Valentin Ivanovich Sergienko
Sergei Ivanovich Shmatko
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OBSCHESTVO S OGRANICHENNOI OTVETSTVENNOSTYU "NAUKA
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Obschestvo S Ogranichennoi Otvetstvennostyu "Nauka - Tekhnologii - Proizvodstvo"
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    • G—PHYSICS
    • G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21F—PROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00—Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/04—Treating liquids
    • G21F9/06—Processing
    • G21F9/16—Processing by fixation in stable solid media
    • G21F9/162—Processing by fixation in stable solid media in an inorganic matrix, e.g. clays, zeolites

Definitions

  • the invention relates to protection of the environment, namely methods for liquid radioactive waste (LRW) reprocessing comprising immobilizing same into a crystal material, acceptable from the viewpoint of ecology and the invention can be used at facilities of atomic power industry and chemical-metalurgical production lines.
  • LRW liquid radioactive waste
  • Liquid radioactive waste reprocessing is connected with the necessity to attain a safe long-term storage of radioactive waste (RAW), for which purpose hard radioactive waste (HRW) change into a state providing for a minimum leaching-out of radionuclides with natural waters.
  • RAW radioactive waste
  • HRW hard radioactive waste
  • This task is solved by conventional methods such as bituminization, cementation and vitrification of RAW (patent RU N 2088986, 27.08.1997 ; patent RU N 2271586, 10,03.2006 ; patent RU N 2131152, 27,05.1999 ; Donald I.W., Metcalfe B.L., Taylor R.N.J. the immobilization of high level radioactive wastes using ceramics and glasses. Review. Journal of Materials Science, 32, 1997. p. 5856-5862 ), The least degree of leaching is provided with RAW vitrification and has a value of about 10 -6 g/cm. day.
  • Such forms of RAW immobilization are ceramic material widely known by the trade name Syncron whose matrix is normally a combination of hollandite (BaAl 2 Ti 2 O 6 or BaAl 2 Ti 6 O 16 ), perovskite (CaTiO 3 ) and zirconolite (CaZrTi2O 7 ).
  • Sorption reactant materials are the new promising materials for the recovery of radionuclides.
  • sorption-reactant materials resides in continuously forming an insoluble compound sorbing radionuclides in a porous matrix of inert material, with a continuous growth of crystals of the insoluble compound concurrently with sorption of the radionuclides.
  • the result there form crystal materials with a very small interface surface and sorbed radionuclides distribute over entire volume of the crystal material; such being the case, the leaching of radionuclides from sorption-reactant materials is by several orders lower than from selective ion- exchange sorbents having a large exchange capacity and, as so, a large interface surface.
  • patent RU N 2185671 20.07.2002 discloses the recovery of strontium radionuclides from solutions with a high content of hardness salts and liquid radioactive wastes of a complex chemical composition.
  • SRMs are formed directly in the process of purification due to reaction of a starting sorption-reactant material comprising barium exchange cations, with a sulfate-ion purifying containing solution with the formation of insoluble barium sulfate crystallzable in the matrix of the sorption-reactant material.
  • An object of the present invention is to provide of a method of reprocessing liquid radioactive wastes containing long-lived radionuclides, preferably cobalt, manganese and strontium in hydrothermal conditions, which provides a high degree, of purification of solutions from radionuclides, as required, a high reparation coefficient (a ratio of purified LRW/HRW volumes), formation of a strong durable ceramic matrix with a minimum leaching-out of the radionuclides.
  • the problem is solved by a method of reprocessing liquid radioactive wastes containing long-lived radionuclides by synthesis of insoluble compounds immobilizing the long-lived radionuclides in hydrothermal conditions in a flow by passing LRW being treamed and reagents required for synthesis thought a layer of insoluble particles at a speed enabling synthesizable radionuclide-containing compounds to be crystallized on the surface of the particles of the layer.
  • the most favorable conditions for hydrothermal synthesis are temperature of 180-250°C and pressure of 20-150 atm.
  • Insoluble particles used arc preferably represented by metal oxides or salts thereof.
  • Metal oxides used arc represented by ferric oxide and/or manganese oxide and/or cobalt oxide and salts, by hydroxylapatite.
  • the problem is solved by a method of reprocessing liquid radioactive wastes containing long-lived radionuclides by synthesis of insoluble compounds immobilizing long-lived radionuclides into a crystal lattice, with synthesis of a crystal phase in the form of oxides in hydrothermal conditions in a flow by passing LRWs being treated and reagents required for the synthesis through a layer of metal oxides at a speed enabling synthesizable radionuclide-containing oxides to be crystallized on the surface of the particles of the layer of oxides.
  • transition metal oxides used are represented by ferric oxide and/or manganese oxide and/or cobalt oxide and/or zirconium oxide.
  • the third alternative embodiment provides the method of reprocessing liquid radioactive wastes containing long-lived radionuclides by synthesis of Insoluble compounds immobilizing the long-lived radionuclides into a crystal lattice in hydrothermal condition, in a flow by passing LRWs being treated and reagent required for the synthesis through a layer of transition metal oxides at a speed enabling synthesizable radionuclide - containing compounds to be crystallized on the surface of the particles of the layer of oxides.
  • transition metal oxides used are represented by ferric oxide and/or manganese oxide and/or cobalt oxide and/or zirconium oxides.
  • composition of synthesizable compounds formable on the surface of particles can be different from the composition of particles of the layer and depends on the composition of an initial solution
  • oxide synthesis is performed through crystallization of a new phase on the surface of particles of a layer, not in the volume of the layer, as is the case with a known method ( RU 2185671 ).
  • oxides appearing on the surface of oxides representing a layer of particles can differ as to a composition thereof from the oxides of the layer and are dependent on the composition of an initial solution.
  • crystallization means the change of a substance from the liquid state to the solid crystal state and the term “crystallization on the surface of particles” is heterogenic formation of a crystal phase on the surface of a solid.
  • phase in the context of the present invention one should imply a generally accepted in the art, uniform in formulatian and properties, part of a thermodynamic system separated from other phases by interfaces on which some of the properties of the system change stepwise,
  • immobilization in the present invention one should imply inclusion of radionuclides in a crystal lattice of insoluble compounds crystallizable on the surface of particles of a layer.
  • a solution of LRW is passed through a layer of particles and on the surface of the layer in hydrothermal conditions, more exactly, at elevated temperature and pressure, now compounds are synthesized in form of crystals which immobilize radionuclides.
  • the speed of passing of LRW solutions through the layer of particles should be such that the formation of crystals on the surface of the layer of immobilizing radionuclide particles provide the desirable degree of purification from the radionuclides.
  • the speed of a flow is greater than a certain value determined experimentally in each and every particular case there occurs crystallization in the volume of a solution but not the surface of particles of the layer and more than that a portion of radionuclides containing crystals arc lift out of the layer and no purification occurs whatsoever.
  • a solution being treated should contain ions forming under hydrothermal conditions the crystals of compounds immobilizing radionuclides-
  • reagents which would supply presence with ions required for the synthesis in the solution are added to the solution of LRW, said reagents being represented by oxidants such as hydrogen peroxide or potassium permanganate, oxidizing ions within the LRWs to an oxidation state of formation of insoluble compounds, and/or metal salts,
  • Fig. 1 shows the ASM-pictures of particles of a layer before hydrothermal synthesis (initial particle), Fig. 2 - in the process of synthesis, Fig. 3 - upon completion of hydrothermal synthesis.
  • a method for any one of the alternative embodiment is realized, as followings.
  • Reagents as required depending on the type of the LRWs being processed are added to the feeding LRW followed by feeding LRWs to the flow reactor for hydrothermal synthesis in which a layer of particles of insoluble compounds is placed.
  • Synthesis is carried out in a temperature range of 180 to 250°C, at a pressure of 20 to 150 atm., which corresponds to the sufficient rate of crystal growth and the desirable degree of purification from radionuclides.
  • the compounds resulting from hydrothermal synthesis are deposited on insoluble particles forming the layer.
  • a radionuclide-free solution is a process radioactive-free waste material.
  • the layered structure of a synthesized compound which grows on an initial globular structure is seen on the pictures.
  • the Invention is illustrated by the following examples.
  • EXAMPLE 1 (Variant 1). LRWs containing 2 g/l Trilon B and 0.5 g/l trisodium phosphate having a 0.1 g/l concentration of calcium ions and comprising strontium-90 radionuclides (1.5 ⁇ 10 -6 Ci/l) are passed through a layer of hydroxylapatite Ca 3 PO 4 -Ca(OH) 2 having a particle size of 0.1-0.3 mm, charged into a healed cylindrical reactor dimensioned 100 x 10 mm. The process is carried out at the flow speed of I ml/min., at the temperature of 200°C and pressure of 100 atm. A solution flow is provided with a chromatographic high pressure pump.
  • EXAMPLE 2 (Variant 2).
  • the bottoms of a nuclear waste evaporators which arc purified from cesium radionuclides by filtration through ferrocyanide sorbets and contained cobalt-60 radionuclides (1 ⁇ 10 -5 Cl/l) and manganese-54 (1 ⁇ 10 -8 Ci/l) arc passed through a layer of iron-cobalt ferrite (iron-cobalt oxides) with an iron to cobalt molar ratio of 1:01 and a particle size of 0.2-0.5 mm charged into a heated cylindrical reactor dimensioned 100 x10 mm. The process is carried out at the flow speed of 2 ml/min., at the temperature of 220°C and pressure of 100 atm.
  • a solution flow is provided with a high pressure chromatographic pump. Simultaneously 6% solution of hydrogen peroxide is added to the reactor by the second high pressure pump at the rate of 0.6 ml/min. Activity of the effluent solution and the leaching coefficients of cobalt radionuclides from the charge of oxides formed, as specified upon completion of a test arc given in Table 2.
  • EXAMPLE 3 (Variant 3). LRWs containing 2 g/l Trilon B and 0.5 g/l trisodium phosphate having a concentration of calcium ions of 0,1 g/l and comprising strontium-90 radionuclides (1.5 ⁇ 10 -6 Ci/l) are passed through a layer of zirconium oxide having a particle size of 0.1-0.3 mm, charged into a heated cylindrical reactor dimensioned 100 x 10 mm. The process proceeds al the speed of a flow of 1 ml/min., at 200°C and the pressure of 100 atm. A section flow is provided with a chlomatographic high pressure pump.
  • EXAMPLE 4 Sea water contaminated with strontium-90 radionuclides, 2 ⁇ 10 -6 Ci Activity, is passed through a layer of manganese dioxide having a particle size of 0.05-0.1 mm, charged in a heated cylindrical reactor dimensioned 100 x 10 mm. The process is carried out at the speed of a flow of 1 ml/min. at 220°C and the pressure of 100 atm. A solution flow is provided with a high pressure chromatographic pump. A solution 0.1 n manganese (II) chloride and 0.1 n potassium permanganate solution were added to the reactor by high pressure pumps at the rate of 0.6 ml/min.
  • EXAMPLE 5 LRWs being decontaminated containing 2 g/l sodium oxalate and 0.5 g/l Trilon B purified from cesium radionuclides by filtration through ferrocyanide sorbents and comprising cobalt 60 (1-10 -7 Ci/l) and strontium-90 (4 ⁇ 10 -7 Ci/l) radionuclides are successively passed though a layer of iron-cobalt ferrite with a molar ratio of iron: cobalt of 1: 0.1 and a particle size of 0.2-0.5 mm, charged in a heated cylindrical reactor dimensioned 100 x 10 mm and through a layer of manganese dioxide having a particle size of 0.05-0.1 mm, charged in the heated cylindrical reactor dimensioned 100 x 10 mm.
  • the process proceeds at the speed of a flow of 1 ml/min, at 200°C and pressure of 100 bar.
  • a solution flow is provided a high pressure chromatographic pump.
  • Simultaneously 6% hydrogen peroxide solution at the rate of 0.6 ml/min is added to the first reactor and 0.1 n manganese (II) chloride solution is added to the second reactor by the high-pressure pump.
  • EXAMPLE 6 Alkali LRWs containing 0.3 g/l sodium hydroxide cobalt-60 (1 ⁇ 10 -7 Ci/l) and cesium - 137 (6 ⁇ 10 -7 Ci/l) radionuclides are passed through a layer of perlite-filter with the contained 3.4% iron, charged in a heated cylindrical reactor dimensioned 100 x 10 mm. The process is conducted at the speed of a flow of 0.3 ml/min. at 170°C and the pressure of 100 atm. A solution flow is provided with the high pressure chromatographic pump.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)
EP07852046.7A 2006-12-06 2007-11-07 Verfahren zur umverarbeitung von flüssigen radioaktiven abfallstoffen Not-in-force EP2101333B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
RU2006143293/06A RU2321909C1 (ru) 2006-12-06 2006-12-06 Способ переработки жидких радиоактивных отходов (варианты)
PCT/RU2007/000614 WO2008069694A1 (fr) 2006-12-06 2007-11-07 Procédé de transformation de déchets radioactifs liquides (et variantes)

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EP2101333A1 true EP2101333A1 (de) 2009-09-16
EP2101333A4 EP2101333A4 (de) 2011-04-13
EP2101333B1 EP2101333B1 (de) 2014-04-30

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RU (1) RU2321909C1 (de)
WO (1) WO2008069694A1 (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110447077A (zh) * 2017-01-16 2019-11-12 俄罗斯联邦诺萨顿国家原子能公司 处理放射性溶液的方法

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2537391C1 (ru) * 2013-07-01 2015-01-10 Федеральное государственное автономное образовательное учреждение высшего профессионального образования "Дальневосточный федеральный университет (ДВФУ) Способ переработки жидких радиоактивных отходов
DE102018114550A1 (de) * 2018-06-18 2019-12-19 Nukem Technologies Engineering Services Gmbh Verfahren zum Vorreinigen von Radionuklide enthaltenden Lösungen

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5926771A (en) * 1994-09-14 1999-07-20 Brown; Paul W. Method of immobilizing toxic or radioactive inorganic wastes and associated products
US20020038070A1 (en) * 2000-06-12 2002-03-28 Anatoly Chekhmir Processes for immobilizing radioactive and hazardous wastes
RU2185671C1 (ru) * 2001-01-10 2002-07-20 Государственное учреждение - Институт химии Дальневосточного отделения РАН Способ извлечения радионуклида стронция из водных растворов (варианты)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3833676A1 (de) * 1988-10-04 1990-04-05 Petri Juergen Dipl Ing Dr Verfahren zur endlagerung von eingebundenen abfallstoffen
JP3074079B2 (ja) * 1992-11-24 2000-08-07 株式会社東芝 放射性廃溶媒の固化処理方法
RU2088986C1 (ru) 1994-12-15 1997-08-27 Всероссийский научно-исследовательский институт неорганических материалов им.акад.А.А.Бочвара Способ отверждения фильтроперлитных пульп
RU2131152C1 (ru) 1998-02-24 1999-05-27 Чечельницкий Геннадий Моисеевич Способ обработки жидких радиоактивных отходов ядерной энергетической установки
RU2212069C2 (ru) * 2001-04-17 2003-09-10 Производственное объединение "МАЯК" Способ отверждения растворов долгоживущих радионуклидов
RU2271586C2 (ru) 2004-04-01 2006-03-10 Федеральное государственное унитарное предприятие "Государственный научный центр Российской Федерации - Физико-энергетический институт им. А.И. Лейпунского" Способ иммобилизации концентрированных жидких радиоактивных отходов (варианты)

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5926771A (en) * 1994-09-14 1999-07-20 Brown; Paul W. Method of immobilizing toxic or radioactive inorganic wastes and associated products
US20020038070A1 (en) * 2000-06-12 2002-03-28 Anatoly Chekhmir Processes for immobilizing radioactive and hazardous wastes
RU2185671C1 (ru) * 2001-01-10 2002-07-20 Государственное учреждение - Институт химии Дальневосточного отделения РАН Способ извлечения радионуклида стронция из водных растворов (варианты)

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2008069694A1 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110447077A (zh) * 2017-01-16 2019-11-12 俄罗斯联邦诺萨顿国家原子能公司 处理放射性溶液的方法
CN110447077B (zh) * 2017-01-16 2023-05-05 俄罗斯联邦诺萨顿国家原子能公司 处理放射性溶液的方法

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Publication number Publication date
EP2101333A4 (de) 2011-04-13
WO2008069694A1 (fr) 2008-06-12
RU2321909C1 (ru) 2008-04-10
EP2101333B1 (de) 2014-04-30

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