EP2374136A2 - Verfahren zum verarbeiten eines stickstoffhaltigen wässrigen flüssigen abwassers durch kalzination und vitrifikation - Google Patents
Verfahren zum verarbeiten eines stickstoffhaltigen wässrigen flüssigen abwassers durch kalzination und vitrifikationInfo
- Publication number
- EP2374136A2 EP2374136A2 EP09804131A EP09804131A EP2374136A2 EP 2374136 A2 EP2374136 A2 EP 2374136A2 EP 09804131 A EP09804131 A EP 09804131A EP 09804131 A EP09804131 A EP 09804131A EP 2374136 A2 EP2374136 A2 EP 2374136A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- nitrate
- calcination
- effluent
- oxide
- nitrates
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000001354 calcination Methods 0.000 title claims abstract description 79
- 238000000034 method Methods 0.000 title claims abstract description 29
- 239000007788 liquid Substances 0.000 title claims abstract description 14
- 238000004017 vitrification Methods 0.000 title claims description 20
- GQPLMRYTRLFLPF-UHFFFAOYSA-N nitrous oxide Inorganic materials [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 title abstract 2
- 238000010790 dilution Methods 0.000 claims abstract description 29
- 239000012895 dilution Substances 0.000 claims abstract description 29
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- 150000002823 nitrates Chemical class 0.000 claims abstract description 28
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910002651 NO3 Inorganic materials 0.000 claims abstract description 23
- 229910052751 metal Inorganic materials 0.000 claims abstract description 19
- 239000002184 metal Substances 0.000 claims abstract description 19
- 229910052752 metalloid Inorganic materials 0.000 claims abstract description 19
- 150000002738 metalloids Chemical class 0.000 claims abstract description 17
- -1 metalloid nitrates Chemical class 0.000 claims abstract description 16
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 claims abstract description 14
- 150000002739 metals Chemical class 0.000 claims abstract description 14
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 12
- 239000002671 adjuvant Substances 0.000 claims description 40
- 239000011521 glass Substances 0.000 claims description 37
- BNGXYYYYKUGPPF-UHFFFAOYSA-M (3-methylphenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].CC1=CC=CC(C[P+](C=2C=CC=CC=2)(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 BNGXYYYYKUGPPF-UHFFFAOYSA-M 0.000 claims description 28
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims description 26
- 239000000203 mixture Substances 0.000 claims description 14
- 235000010344 sodium nitrate Nutrition 0.000 claims description 13
- 239000004317 sodium nitrate Substances 0.000 claims description 13
- HSJPMRKMPBAUAU-UHFFFAOYSA-N cerium(3+);trinitrate Chemical compound [Ce+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O HSJPMRKMPBAUAU-UHFFFAOYSA-N 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 8
- FYDKNKUEBJQCCN-UHFFFAOYSA-N lanthanum(3+);trinitrate Chemical compound [La+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O FYDKNKUEBJQCCN-UHFFFAOYSA-N 0.000 claims description 5
- CFYGEIAZMVFFDE-UHFFFAOYSA-N neodymium(3+);trinitrate Chemical compound [Nd+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O CFYGEIAZMVFFDE-UHFFFAOYSA-N 0.000 claims description 5
- YWECOPREQNXXBZ-UHFFFAOYSA-N praseodymium(3+);trinitrate Chemical compound [Pr+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O YWECOPREQNXXBZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- DHRLEVQXOMLTIM-UHFFFAOYSA-N phosphoric acid;trioxomolybdenum Chemical compound O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.O=[Mo](=O)=O.OP(O)(O)=O DHRLEVQXOMLTIM-UHFFFAOYSA-N 0.000 claims description 3
- XWROSHJVVFETLV-UHFFFAOYSA-N [B+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O Chemical compound [B+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O XWROSHJVVFETLV-UHFFFAOYSA-N 0.000 claims description 2
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 2
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 2
- JLDSOYXADOWAKB-UHFFFAOYSA-N aluminium nitrate Chemical compound [Al+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O JLDSOYXADOWAKB-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000654 additive Substances 0.000 abstract 2
- 230000000996 additive effect Effects 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 229910052742 iron Inorganic materials 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 239000002699 waste material Substances 0.000 description 6
- 238000010348 incorporation Methods 0.000 description 5
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000009472 formulation Methods 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000002285 radioactive effect Effects 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 229910052777 Praseodymium Inorganic materials 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005672 electromagnetic field Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 150000002505 iron Chemical class 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 229910001960 metal nitrate Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- PUDIUYLPXJFUGB-UHFFFAOYSA-N praseodymium atom Chemical compound [Pr] PUDIUYLPXJFUGB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- G21F9/14—Processing by incineration; by calcination, e.g. desiccation
-
- 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
- G21F9/28—Treating solids
- G21F9/30—Processing
- G21F9/301—Processing by fixation in stable solid media
- G21F9/302—Processing by fixation in stable solid media in an inorganic matrix
- G21F9/305—Glass or glass like matrix
Definitions
- the invention relates to a process for the treatment of a liquid aqueous nitrate effluent, generally containing mainly sodium nitrate with nitrates of metals or metalloids, which comprises a calcination step generally followed by a vitrification step of the calcine obtained during said calcination step.
- the technical field of the invention can be defined generally as that of the calcination of liquid effluents, more particularly the technical field of the invention can be defined as the calcination of radioactive liquid effluents for their vitrification.
- the French vitrification process for radioactive liquid effluents comprises two steps.
- the first step is a step of calcining the effluent during which a drying and then a denitration of a portion of the nitrates takes place.
- the second step is a vitrification step by dissolving in a glass of containment the calcine produced during the calcination step.
- the calcination step is generally carried out in a rotary tube heated to 400 ° C. by an electric furnace. Solid calcine is crushed by a crazy bar placed inside the rotating tube.
- this aluminum nitrate added to the effluent increases the amount of glass to be produced. Indeed, the presence of alumina in the glass increases its production temperature and leads to limit the rate of waste load, effluent in the glass, so as not to degrade the confinement properties of this glass.
- the aluminum content in the glass must not be too high and is generally limited to about 15% by weight expressed as Al 2 O 3.
- the amount of aluminum nitrate to be added is also difficult to optimize, so for each new effluent, several tests are necessary to determine the operating conditions of heated rotating tube calcination to avoid clogging of the tube. In particular, it is necessary to adjust the heating of the calcination furnace and the quantities of calcination aid, which is different dilution adjuvant, which is very often sugar.
- the object of the present invention is to provide a method for treating an aqueous nitrate liquid effluent containing nitrates of metals or metalloids, this process comprising a step of calcining the effluent to transform the nitrates of metals or metalloids into their oxides, which, among other things, meet the needs mentioned above.
- the object of the present invention is still to provide such a method which does not have the drawbacks, limitations, defects and disadvantages of the processes of the prior art and which solves the problems of the processes of the prior art, in particular methods aluminum nitrate is used as a dilution adjuvant.
- a method of treating an aqueous nitrate liquid effluent containing nitrates of metals or metalloids comprising a step of calcining the effluent to transform the nitrates of metals or metalloids to oxides of metals or metalloids, at least one compound selected from nitrates of metals or metalloids and other compounds of the effluent resulting in calcination with a sticky oxide, and a dilution adjuvant leading during calcination with a non-sticky oxide being added to the effluent prior to the calcination step, in which process the adjuvant dilution comprises aluminum nitrate and at least one other nitrate selected from iron nitrate and rare earth nitrates.
- the dilution adjuvant consists of aluminum nitrate and at least one other nitrate selected from iron nitrate and rare earth nitrates.
- the process according to the invention is fundamentally characterized by the use, during calcination, of a particular dilution adjuvant which comprises, in addition to aluminum nitrate, at least one specific nitrate chosen from iron nitrate and rare earth nitrates.
- iron nitrate and rare earth nitrates have calcination bond limiting properties close to those of aluminum nitrate, but that the oxides derived from these specific nitrates, which are so-called “non-sticky” oxides, can also dissolve in the final glass produced during the subsequent vitrification step.
- a dilution adjuvant comprising a nitrate chosen from iron nitrate and rare earth nitrates in substitution for part of the aluminum nitrate thus makes it possible to prevent clogging of the calcination apparatus tube. during the calcination of effluents generating highly sticky oxides, such as solutions with high sodium content, while minimizing the increase in the amount of confining glass to be produced during the vitrification step which generally follows the calcination.
- iron nitrate and rare earth nitrates exhibit all the excellent properties of aluminum nitrate in its ability to limit calcine bonding, and thus to avoid clogging of the calcination tube. and have an advantage in reducing the amount of glass to be produced and increasing the rate of waste charge incorporated in the glass.
- the constraints imposed on the glass formulation by the dilution adjuvants according to the invention comprising, in substitution of a portion of the aluminum nitrate, at least one specific nitrate selected from iron nitrate and rare earth nitrates are markedly reduced. compared to dilution adjuvants consisting solely of aluminum nitrate because of the lower or no aluminum intake.
- Rare earth nitrates are generally chosen from lanthanum nitrate, cerium nitrate, praseodymium nitrate, and neodymium nitrate; and therefore the dilution adjuvant may advantageously comprise aluminum nitrate and at least one other nitrate selected from nitrate of iron, lanthanum nitrate, cerium nitrate, praseodymium nitrate and neodymium nitrate.
- the dilution adjuvant consists of aluminum nitrate and at least one other nitrate selected from iron nitrate, lanthanum nitrate, cerium nitrate, praseodymium nitrate and neodymium nitrate.
- a particularly preferred dilution adjuvant according to the invention consists of aluminum nitrate and iron nitrate.
- Another particularly preferred dilution adjuvant according to the invention consists of aluminum nitrate, lanthanum nitrate, neodymium nitrate, cerium nitrate and praseodymium nitrate.
- each of the aluminum, iron, and rare earth nitrates are free from the point of view of their effectiveness in preventing the bonding of the calcine in the tube and can therefore be adjusted according to their impact on the properties of the containment glass prepared in a subsequent vitrification step.
- the amount of dilution adjuvant added to the liquid effluent is a function of the contents of sticky compounds of the liquid effluent (nitrates and / or other compounds), expressed in terms of oxides, of the total mass of the nitrates (or possibly more precisely, the total mass of salts), also expressed in terms of oxides, contained in the effluent.
- the effluent is generally composed mainly of a mixture of metal nitrates and metalloids with a majority of sodium nitrate and may also contain a quantity of aluminum nitrates, iron and rare earths in contents insufficient to prevent clogging of the tube during the calcination step.
- the effluent may also contain "sticky” or “non-sticky” compounds which are not nitrates, generally present in the form of salts, such as phosphomolybdic acid which is a so-called “sticky” compound.
- the method according to the invention because of the implementation of the specific dilution adjuvant mentioned above allows the calcination without clogging of all kinds of effluents, whatever their nature and the nature of the nitrates and nitrates sticky which there are contained.
- the liquid effluent treated by the process according to the invention contains at least one compound such as a nitrate of metal or metalloid leading during calcination to a so-called “sticky” oxide, such as sodium nitrate, and / or another compound (which is not a nitrate) leading during calcination to a so-called “sticky” oxide.
- a nitrate of metal or metalloid leading during calcination to a so-called "sticky” oxide, such as sodium nitrate, and / or another compound (which is not a nitrate) leading during calcination to a so-called “sticky” oxide.
- sticky compounds means compounds, oxides, nitrates known to stick to the walls of "calciner” calcination apparatus and induce clogging phenomena of these calcinators.
- the compound (s), such as (the) nitrate (s) and / or the other compound (s), which leads (conduct) upon calcination to may sticky oxide (s) be (may they) be selected from sodium nitrate, phosphomolybdic acid, boron nitrate and mixtures thereof.
- the content of the compound (s), such that (these) nitrate (s) and other compound (s) leading during the calcination to (or) "sticky" oxide (s) in the effluent, expressed as oxide, relative to the total mass of salts, including nitrates, contained in the effluent, also expressed as oxide, is generally greater than 35% by mass.
- the process according to the invention makes it possible, in particular, for the calcination of effluents having a high content of nitrates and other compounds, called "stickiness", ie greater than 35% by weight, expressed as oxides.
- the process according to the invention allows the calcination of high sodium solutions which are very tacky.
- “High sodium”, more specifically sodium nitrate, is generally understood to mean that the effluent has a sodium nitrate content, expressed as sodium oxide Na2 ⁇ 0, relative to the total mass of the salts, including the nitrates contained in the effluent, expressed in oxides, greater than 30% by weight, preferably greater than 50% by weight.
- the calcination conditions are generally as follows: temperature reached by the calcine at about 400 ° C., rotation speed of the tube at 40 rpm, addition of a calcination aid, for example of the sugar type.
- This calcination step is generally carried out in a heated rotating tube, for example a rotating tube heated by an electric furnace with several independent heating zones. Heating zones are more particularly dedicated to evaporation and others to calcination.
- Calcining zones can heat the calcine at a temperature of about 400 0 C.
- the speed of rotation of the tube, the addition of the calcination aid and the presence of an idle bar makes it possible to divide the solid calcine so that it can react under good conditions in the vitrification unit.
- the treatment process according to the invention generally comprises, after the calcination step, a vitrification step of the calcine obtained during this calcination step.
- This vitrification step consists of a reaction between the calcine and a glass frit (preformed glass) to obtain a confinement glass.
- a vitrification step is carried out which consists of producing a confinement glass from the melting of the calcine produced during the calcination step with glass frit.
- the use in the dilution adjuvant of specific nitrates of iron and rare earths makes it possible to relax the constraints with regard to the formulation of the glass.
- a higher proportion of effluent in the glass can be incorporated when the calcine was obtained using the dilution adjuvant according to the invention in place of a dilution adjuvant consisting solely of aluminum nitrate.
- the binding limit on the rate of incorporation of effluents into the glass, due to aluminum nitrate, is eliminated, and the rate of incorporation is significantly increased and passes through.
- Vitrification consists of a melting reaction between the calcine and the glass frit to form a confining glass.
- indirect induction furnaces which consist in heating by four inductors a metal pot into which the sintered / calcined mixture is introduced
- direct induction furnaces which consist of heating the glass by an inductor to through a cooled structure (cold crucible) which passes a part of the electromagnetic field and in which is introduced continuously the sintered mixture / calcinate.
- the percentage of oxides is expressed in relation to the total mass of the oxides corresponding to the salts contained in the effluent.
- adjuvant 1 of the prior art which consists of 100% by weight of aluminum nitrate expressed as Al 2 O 3 oxide.
- the temperature reached by the calcine is about 400 ° C.
- the speed of rotation of the rotating tube containing the idler bar is 20 rpm
- the calcination aid content is 40 g Of the mixture of the effluent with the dilution adjuvant.
- adjuvant 2 which consists of 75% by weight of aluminum nitrate expressed as Al 2 O 3 oxide. and 25% by weight of iron nitrate expressed as Fe 2 O 3 oxide.
- adjuvant No. 1 an adjuvant consisting solely of aluminum nitrate.
- Example 2 the vitrification of the calcine obtained in Example 2 according to the invention is carried out.
- this calcine was prepared using an adjuvant ("adjuvant No. 2") consisting of 75% by weight of aluminum salt and 25% by weight of iron salt.
- the high intake of aluminum by the adjuvant No. 1 tends to harden the calcine and results in a slight decrease in reactivity between the calcine and the glass frit in the vitrification furnace.
- adjuvant 3 in which part of the aluminum nitrate has been replaced by a mixture of nitrates of lanthanum, cerium, neodymium and praseodymium.
- the content of sodium nitrate expressed as total oxide mass represents 30% in the mixture of the effluent with the dilution adjuvant.
- the conditions of calcination are as follows:
- the temperature reached by the calcine is approximately 350 ° C.
- the speed of rotation of the rotating tube containing the idler bar is 35 rpm
- the calcination aid content is 20 g Of the mixture of the effluent with the dilution adjuvant.
Landscapes
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- High Energy & Nuclear Physics (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Catalysts (AREA)
- Compounds Of Alkaline-Earth Elements, Aluminum Or Rare-Earth Metals (AREA)
- Removal Of Specific Substances (AREA)
- Glass Compositions (AREA)
- Luminescent Compositions (AREA)
- Processing Of Solid Wastes (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0859134A FR2940716B1 (fr) | 2008-12-30 | 2008-12-30 | Procede de traitement d'un effluent liquide aqueux nitrique par calcination et vitrification |
| PCT/EP2009/067899 WO2010076286A2 (fr) | 2008-12-30 | 2009-12-23 | Procede de traitement d'un effluent liquide aqueux nitrique par calcination et vitrification |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2374136A2 true EP2374136A2 (de) | 2011-10-12 |
| EP2374136B1 EP2374136B1 (de) | 2012-11-14 |
Family
ID=41100799
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09804131A Active EP2374136B1 (de) | 2008-12-30 | 2009-12-23 | Verfahren zum verarbeiten eines stickstoffhaltigen wässrigen flüssigen abwassers durch kalzination und vitrifikation |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8604264B2 (de) |
| EP (1) | EP2374136B1 (de) |
| JP (1) | JP5818255B2 (de) |
| KR (1) | KR101698189B1 (de) |
| CN (1) | CN102265353B (de) |
| ES (1) | ES2399802T3 (de) |
| FR (1) | FR2940716B1 (de) |
| RU (1) | RU2531637C2 (de) |
| WO (1) | WO2010076286A2 (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2940717B1 (fr) * | 2008-12-30 | 2011-09-23 | Areva Nc | Procede de traitement d'un effluent liquide aqueux nitrique par calcination et vitrification |
| CN102592694A (zh) * | 2012-03-15 | 2012-07-18 | 西南科技大学 | 一种高放后处理氧化物的大容量复合固化方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3008904A (en) * | 1959-12-29 | 1961-11-14 | Jr Benjamin M Johnson | Processing of radioactive waste |
| US3272756A (en) * | 1965-08-31 | 1966-09-13 | John D Kaser | Radioactive waste disposal using colemanite |
| US3943062A (en) * | 1974-05-13 | 1976-03-09 | The United States Of America As Represented By The United States Energy Research And Development Administration | Cryolite process for the solidification of radioactive wastes |
| GB1492464A (en) * | 1975-01-28 | 1977-11-23 | Us Energy | Process for calcining radioactive wastes containing sodium nitrate |
| JPS5263867A (en) * | 1975-11-21 | 1977-05-26 | Mitsui Eng & Shipbuild Co Ltd | Treating method of waste gas containing sodium nitrate |
| JPS53109100A (en) * | 1977-03-03 | 1978-09-22 | Power Reactor & Nuclear Fuel Dev Corp | Treatmetn method of high level radioactive waste solution cantaining sodium nitrate |
| US4164479A (en) * | 1978-01-12 | 1979-08-14 | The United States Of America As Represented By The United States Department Of Energy | Method for calcining nuclear waste solutions containing zirconium and halides |
| JPS6046394B2 (ja) * | 1981-07-06 | 1985-10-15 | 工業技術院長 | 高レベル放射性廃液のガラスによる固化処理方法 |
| JPS61132898A (ja) * | 1984-11-30 | 1986-06-20 | 株式会社東芝 | 放射性廃棄物の固化処理方法 |
| JPH0648314B2 (ja) * | 1987-02-13 | 1994-06-22 | 動力炉・核燃料開発事業団 | 放射性廃液の処理方法 |
| JPS63300999A (ja) * | 1987-05-30 | 1988-12-08 | Mitsubishi Metal Corp | 硝酸ナトリウムを含有する放射性廃物質の処理方法 |
| RU2203512C2 (ru) * | 2000-10-18 | 2003-04-27 | Федеральное государственное унитарное предприятие "Всероссийский научно-исследовательский институт неорганических материалов им. акад. А.А. Бочвара" | Способ отверждения жидких радиоактивных отходов и устройство для его осуществления |
| RU2201629C2 (ru) * | 2001-01-09 | 2003-03-27 | Государственное унитарное предприятие Научно-производственное объединение "Радиевый институт им. В.Г.Хлопина" | Способ отверждения концентрата трансплутониевых или трансплутониевых и редкоземельных элементов в металлокерамику |
| FR2888576B1 (fr) | 2005-07-15 | 2007-09-28 | Commissariat Energie Atomique | Procede de confinement d'une matiere par vitrification |
| FR2906927B1 (fr) | 2006-10-05 | 2014-07-25 | Commissariat Energie Atomique | Procede de vitrification de produits de fission. |
-
2008
- 2008-12-30 FR FR0859134A patent/FR2940716B1/fr not_active Expired - Fee Related
-
2009
- 2009-12-23 WO PCT/EP2009/067899 patent/WO2010076286A2/fr not_active Ceased
- 2009-12-23 EP EP09804131A patent/EP2374136B1/de active Active
- 2009-12-23 JP JP2011544032A patent/JP5818255B2/ja active Active
- 2009-12-23 US US13/142,804 patent/US8604264B2/en not_active Expired - Fee Related
- 2009-12-23 KR KR1020117017673A patent/KR101698189B1/ko active Active
- 2009-12-23 ES ES09804131T patent/ES2399802T3/es active Active
- 2009-12-23 RU RU2011132010/07A patent/RU2531637C2/ru active
- 2009-12-23 CN CN200980152167.7A patent/CN102265353B/zh active Active
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2010076286A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2011132010A (ru) | 2013-02-10 |
| CN102265353B (zh) | 2014-11-12 |
| WO2010076286A3 (fr) | 2010-09-16 |
| EP2374136B1 (de) | 2012-11-14 |
| JP2012514205A (ja) | 2012-06-21 |
| FR2940716A1 (fr) | 2010-07-02 |
| JP5818255B2 (ja) | 2015-11-18 |
| KR20110100303A (ko) | 2011-09-09 |
| FR2940716B1 (fr) | 2011-09-23 |
| US8604264B2 (en) | 2013-12-10 |
| RU2531637C2 (ru) | 2014-10-27 |
| CN102265353A (zh) | 2011-11-30 |
| WO2010076286A2 (fr) | 2010-07-08 |
| ES2399802T3 (es) | 2013-04-03 |
| US20110306817A1 (en) | 2011-12-15 |
| KR101698189B1 (ko) | 2017-01-19 |
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