EP0204634B1 - Verfahren und Einrichtung zum Behandeln von nichtorganischen festen Tritium enthaltenden Abfällen - Google Patents

Verfahren und Einrichtung zum Behandeln von nichtorganischen festen Tritium enthaltenden Abfällen Download PDF

Info

Publication number
EP0204634B1
EP0204634B1 EP19860401184 EP86401184A EP0204634B1 EP 0204634 B1 EP0204634 B1 EP 0204634B1 EP 19860401184 EP19860401184 EP 19860401184 EP 86401184 A EP86401184 A EP 86401184A EP 0204634 B1 EP0204634 B1 EP 0204634B1
Authority
EP
European Patent Office
Prior art keywords
waste
gases
detritiation
hydrogen
bringing
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.)
Expired - Lifetime
Application number
EP19860401184
Other languages
English (en)
French (fr)
Other versions
EP0204634A1 (de
Inventor
Pierre Giroux
Michel Maj
Gilbert Theis
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Commissariat a lEnergie Atomique et aux Energies Alternatives CEA
Original Assignee
Commissariat a lEnergie Atomique CEA
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Commissariat a lEnergie Atomique CEA filed Critical Commissariat a lEnergie Atomique CEA
Publication of EP0204634A1 publication Critical patent/EP0204634A1/de
Application granted granted Critical
Publication of EP0204634B1 publication Critical patent/EP0204634B1/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/28Treating solids
    • G21F9/30Processing
    • G21F9/308Processing by melting the waste
    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F9/00Treating radioactively contaminated material; Decontamination arrangements therefor
    • G21F9/02Treating gases

Definitions

  • the subject of the present invention is a method and a device for the treatment of non-organic solid waste having been in contact with tritium or having contained tritiated products.
  • document US Pat. No. 4,285,891 describes a method for removing fission gases such as tritium, krypton, xenon and iodine from an irradiated fuel.
  • an inert gas or mixture of inert gases containing hydrogen is passed in contact with the fuel in order to remove the tritium.
  • the inert gas or the mixture of inert gases alone, that is to say containing no hydrogen, is then passed through in order to remove the other products, the operation being carried out at a temperature above 1000 ° C. .
  • Document DE-A 2 434 876 also discloses a process for removing tritium and its compounds contained in a gas stream, in the. which the gas stream is passed through a reactor where it undergoes catalytic combustion to transform the tritium into tritiated water. The gas stream then passes over one or more dryers which retain water, including tritiated water.
  • the present invention specifically relates to a process for treating tritiated waste which is simple and easy to implement and which makes it possible to considerably reduce the tritium content of the treated parts. It also makes it possible to homogenize the residual content, which facilitates the measurement of this content.
  • hydroxogen used in the present description designates all the isotopes of this element, that is to say as well hydrogen as deuterium or tritium.
  • the oxidation of these elements therefore makes it possible to obtain either water, or heavy water, or tritiated water, or a mixture of the different molecular species.
  • the role of the molecular sieve is to retain the water molecules formed during contact with the oxidation catalyst, which makes it possible to trap, among other things, tritiated water. This is then subjected to further processing.
  • the airlock is in the form of a bell that can pivot relative to the tank.
  • the means for bringing the gases released during the melting to the detritiation unit comprise at least one pumping group connected to the tank of the furnace by a first pipe and to the detritiation unit. by a second pipe.
  • This pumping group can be a combination of primary pumps and / or secondary pumps. It must be particularly tight vis-à-vis the outside and contain the minimum of organic materials, in particular the minimum of lubricating oil or grease in the parts in contact with the fluid. This relates more particularly to gaseous tritium, tritiated water vapor and possibly tritiated hydrocarbons.
  • the availability sitive object of the invention first comprises an oven, bearing the general reference 2, placed inside a glove box 4.
  • This oven consists essentially of a tank 6 arranged horizontally and open at its upper part .
  • this tank is made of double-walled stainless steel and is cooled by a circulation of water.
  • a crucible 12 made of refractory material which contains the tritiated waste 14. These are heated by induction using a coil 16 when their nature allows. If it is aluminum waste, a graphite crucible can be used to achieve electromagnetic coupling. In this case, the temperature of the liquid mass is of the order of 900 ° C.
  • the liquid mass is at a temperature of the order of 1600 ° C.
  • graphite can be added to the waste in order to facilitate the realization of the electromagnetic coupling.
  • carbon can combine with iron to give a carbide with a lower melting point than stainless steel.
  • the tank 6 is closed by a vacuum valve 18, which is surmounted by an airlock 20 used for the introduction of the products to be treated.
  • the airlock 20 is in the form of a bell open downwards and which can pivot around an axis 22.
  • the airlock is thus movable between an open position 20a shown in lines mixed in the figure and a closed position 20b shown in solid lines.
  • a nacelle 13 containing the waste is introduced inside the airlock from below, when the latter is in the open position, thanks to a cable 24.
  • the mold is filled by pivoting the crucible 12.
  • a pipe 26 equipped with a valve 28 places the tank 6 of the oven in communication with a pumping assembly 30 which, in the example shown here, comprises a primary pump 32 and a secondary pump 34.
  • a pumping assembly 30 which, in the example shown here, comprises a primary pump 32 and a secondary pump 34.
  • These pumps allow on the one hand to create a vacuum inside the furnace and, on the other hand, to send the gases released during the melting of the waste 14 to the detritiation unit 36 which will be described later in the remainder of this text.
  • the primary pump 32 or the secondary pump 34 is used, depending on whether one wishes to obtain a more or less high vacuum. It is also possible to sweep the tank 6 with an appropriate gas, for example argon, hydrogen, dry air or helium.
  • a compressed gas bottle 17 placed outside of the glove box 4 and connected to the tank 6 by a pipe 19 while the pumping group 30 remains on the way in order to constantly extract the gases contained in the enclosure 6.
  • it can be maintained under a reduced pressure of the order of 300 millibars, or under a primary vacuum, the pressure being less than 1 millibar.
  • the pumping assembly 30 is connected to the detritiation assembly 36 by a pipe 38 fitted with a valve 40.
  • the pipe 38 opens into a container 42, which contains an oxidation catalyst 46 This may be, for example, a product from the Deoxo series marketed by the ENGELHARD Company.
  • a line 48 connects the container 42 to two containers 50 placed in parallel and each containing a molecular sieve 52.
  • the gases having passed through the detritiation assembly 36 and leaving at the bottom of the containers 50 are extracted through a line 54 connected to an extraction device.
  • a regeneration device 53 comprises a cold trap and a circulation pump. It allows a counter-current circulation of dry air in the molecular sieves. This is how the dry air goes from the regenerator 53 to the bottom of the containers 50, passes through the molecular sieves 52 from bottom to top and returns to the regenerator 53 by a pipe 57.
  • the line 48 is equipped with a heat exchanger 49 in order to cool the gases leaving the container 42 containing the oxidation catalyst 46.
  • the airlock is then emptied by means of the pumping group.
  • the vacuum valve is withdrawn and the airlock is in direct communication with the tank 6.
  • the basket 13 is then lowered inside the crucible 12.
  • the main advantage of the airlock is that it allows the successive introduction of several charges without. stop the heating means and without breaking the vacuum.
  • the waste to be treated when placed in bulk, occupies a significant volume since it is essentially containers, pipes, taps, valves, etc. When they are melted, the molten mass (and therefore the solid mass which will result from it after solidification) is much more compact and occupies only part of the volume of the crucible. This is why it is possible to carry out several loads during the same operation in order to completely fill the crucible 12.
  • the tank 6 of the oven is closed in a sealed manner by the vacuum valve. 18 and the vacuum still prevails inside the tank.
  • the nacelle itself melts with the waste and that it is therefore preferable to make it from a light and inexpensive material whose melting point is compatible with that of the waste to be treated.
  • the gases contained in the enclosure 6 are constantly released during the melting and are evacuated by the pumping group 30.
  • tritium is a gas and that l tritiated water vaporizes, this has the effect of removing most of the tritium or tritiated water absorbed in the waste.
  • the gases are sent, through the pipe 38, to the container 42. During their passage through this container, they are in contact with the oxidation catalyst 46, which has the effect of oxidizing the isotopes of hydrogen and in particular to transform tritium into tritiated water.
  • This tritiated water which is in the form of vapor, then passes along the pipe 48 and passes through the containers 50 which contain the molecular sieves 52. During the passage of the gases through these molecular sieves, these retain all the vapor of water, and therefore tritiated water which will then undergo a special treatment.
  • the method and the device which are the subject of the invention have particularly advantageous advantages, the main one of which is that they make it possible to obtain a metallic mass in which the level of tritium (and therefore the activity) has been considerably reduced. This is primarily due to the fact that most of the tritium was removed with the gases during the melting. On the other hand, the waste which initially occupied a large volume and had a large contact surface with air, is found, after fusion and solidification, in the form of a compact mass of small volume and having a contact surface. with little importance. As the degassing rate of the tritiated compounds is proportional to the surface, this rate is considerably reduced by the transformation of a mass of waste into a compact and homogeneous mass. In addition, while in the pipes, valves, containers from the dismantling of the factory, the contamination is extremely variable, the latter is homogeneous in the solid mass obtained after the fusion. We can therefore know the contamination rate by making a single measurement.

Landscapes

  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Processing Of Solid Wastes (AREA)
  • Catalysts (AREA)

Claims (7)

1. Verfahren zur Behandlung von festen und schmelzbaren, Tritium enthaltenden Abfällen, dadurch gekennzeichnet, daß es die folgenden Schritte umfaßt:
- Schmelzenlassen der Abfälle (14) im Inneren einer Umhüllung (6), wobei ein Wasserstoffstrom in das Innere der Schmelze der Abfallmasse (14) eingeleitet wird, so daß ein Durchblasen von Wasserstoff in der Schmelze der Abfallmasse erfolgt, wobei der Wasserstoff sowie die in der Abfallmasse absorbierten Gase ständig aus der Umhüllung abgezogen werden, und
- Unterwerfung der abgezogenen Gase einer Behandlung zur Entfernung von Tritium, welche darin besteht, daß diese Gase in Kontakt mit einem Oxidationskatalysator gebracht werden, um den Wasserstoff in Wasserdampf zu transformieren und diesen Wasserdampf über eine Molekularfalle abzufangen.
2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß die Umhüllung (6) von einem Gasstrom durchspült wird.
3. Vorrichtung zur Behandlung von festen und schmelzbaren, Tritium enthaltenden Abfällen, dadurch gekennzeichnet, daß sie umfaßt:
(1) einen Ofen zum Schmelzen der Abfälle (14), welcher aufweist:
- ein Gefäß (6) zur Aufnahme eines die Abfälle (14) enthaltenden Schmelztiegels (12),
- Mittel zum Heizen (16),
- ein das Gefäß (6) verschließendes Vakuumventil (18) und
- eine Schleuse (20) zum Einbringen der Abfälle, wobei diese Schleuse (20) zwischen einer Öffnungsstellung (20a) und einer Schließstellung (20b) verstellbar ist und über das Vakuumventil (18) von dem Gefäß (6) abgetrennt ist, wenn es sich in der Schließstellung befindet;
(2) Mittel zum Durchblasen von Wasserstoff in der Schmelze der Abfallmasse; (3) eine Anordnung zur Entfernung von Tritium
(36) aus den beim Schmelzen freigesetzten Gasen, welche aufweist:
- mindestens einen Rezipienten (42) mit einem Oxidationskatalysator (46) und
- mindestens einen Rezipienten (50) mit einer Molekularfalle (52); und
(4) Mittel (32, 34), um die beim Schmelzen freigesetzten Gase der Anordnung zum Entfernen von Tritium (36) zuzuführen.
4. Vorrichtung nach Anspruch 3, dadurch gekennzeichnet, daß die Schleuse (20) sich in Form einer Glocke darstellt, welche gegenüber dem genannten Gefäß (6) schwenkbar ist.
5. Vorrichtung nach einem der Ansprüche 3 und 4, dadurch gekennzeichnet, daß die Mittel zum Zuführen der beim Schmelzen freigesetzten Gase zur Anordnung zur Entfernung von Tritium (36) mindestens eine Pumpe (32) umfassen, welche mit dem Gefäß (6) des Ofens (2) über eine erste Leitung (26) und mit der Anordnung zur Entfernung von Tritium (36) über eine zweite Leitung (38) verbunden ist.
6. Vorrichtung nach Anspruch 5, dadurch ge- kennzeichnet, daß die Pumpe eine Primärpumpe (32) ist.
7. Vorrichtung nach Anspruch 6, dadurch gekennzeichnet, daß die Mittel zum Zuführen der beim Schmelzen freigesetzten Gase zur Anordnung zur Entfernung von Tritium (36) außerdem eine Sekundärpumpe (34) umfassen, welche mit der Primärpumpe (32) verbunden ist.
EP19860401184 1985-06-07 1986-06-03 Verfahren und Einrichtung zum Behandeln von nichtorganischen festen Tritium enthaltenden Abfällen Expired - Lifetime EP0204634B1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8508666A FR2583208B1 (fr) 1985-06-07 1985-06-07 Procede et dispositif pour le traitement de dechets trities solides non organiques
FR8508666 1985-06-07

Publications (2)

Publication Number Publication Date
EP0204634A1 EP0204634A1 (de) 1986-12-10
EP0204634B1 true EP0204634B1 (de) 1990-05-23

Family

ID=9320007

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19860401184 Expired - Lifetime EP0204634B1 (de) 1985-06-07 1986-06-03 Verfahren und Einrichtung zum Behandeln von nichtorganischen festen Tritium enthaltenden Abfällen

Country Status (5)

Country Link
EP (1) EP0204634B1 (de)
JP (1) JPS61284697A (de)
DE (1) DE3671563D1 (de)
ES (1) ES8801473A1 (de)
FR (1) FR2583208B1 (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2620262B1 (fr) * 1987-09-09 1989-11-17 Commissariat Energie Atomique Procede et installation de traitement de dechets organiques solides contamines par du tritium
DE3930420C1 (en) * 1989-09-12 1990-11-22 Bundesrepublik Deutschland, Vertreten Durch Den Bundesminister Der Verteidigung, Dieser Vertreten Durch Den Praesidenten Des Bundesamtes Fuer Wehrtechnik Und Beschaffung, 5400 Koblenz, De Radioactive waste tritium sepn. - by flushing in gas flow with oxygen, heating and passing tritium through water
DE4029222C1 (en) * 1990-09-14 1991-08-22 Bundesrepublik Deutschland, Vertreten Durch Den Bundesminister Der Verteidigung, Dieser Vertreten Durch Den Praesidenten Des Bundesamtes Fuer Wehrtechnik Und Beschaffung, 5400 Koblenz, De Economical and efficient tritium sepn. - involves passing gas to molten electrodes to ionise molecules, wash tower for absorption and condensate prodn.
LU87907A1 (de) * 1991-03-13 1992-11-16 Euratom Verfahren zum aufarbeiten von absorberstaeben aus wassergekuehlten kernreaktoren
IT1400531B1 (it) * 2010-06-22 2013-06-11 Commissariat Energie Atomique Processo per la detriziazione di soft housekeeping waste e impianto relativo
FR2974444B1 (fr) * 2011-04-21 2015-11-27 Commissariat Energie Atomique Dispositif et procede de detritiation
FR3101558B1 (fr) 2019-10-03 2021-10-22 Onet Tech Cn Procédé pour décontaminer une pièce métallique contenant un gaz par irradiation laser dans un milieu liquide

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1096072A (en) * 1964-02-27 1967-12-20 Atomic Energy Authority Uk Improvements in or relating to incinerators
US4178350A (en) * 1973-08-27 1979-12-11 Engelhard Minerals & Chemicals Corp. Removal of tritium and tritium-containing compounds from a gaseous stream
US4285891A (en) * 1979-12-31 1981-08-25 Exxon Nuclear, Inc. Method of removing fission gases from irradiated fuel
DE3011602A1 (de) * 1980-03-26 1981-10-08 Kernforschungsanlage Jülich GmbH, 5170 Jülich Verfahren und vorrichtung zur endlagerung von tritium, insbesondere tritiumabfaellen aus kernkraftwerken, mit der moeglichkeit der tritiumrueckgewinnung

Also Published As

Publication number Publication date
FR2583208B1 (fr) 1992-04-24
ES555832A0 (es) 1987-12-16
FR2583208A1 (fr) 1986-12-12
ES8801473A1 (es) 1987-12-16
EP0204634A1 (de) 1986-12-10
DE3671563D1 (de) 1990-06-28
JPS61284697A (ja) 1986-12-15

Similar Documents

Publication Publication Date Title
EP3031054B1 (de) Verfahren und vorrichtung zur verbrennung, verschmelzung und verglasung von organischem und metllischem abfall
EP0451050B1 (de) Verfahren und Einrichtung zur Wärmebehandlung mit Gasabschreckung
EP0204634B1 (de) Verfahren und Einrichtung zum Behandeln von nichtorganischen festen Tritium enthaltenden Abfällen
EP0012074A1 (de) Verfahren zur Reinigung einer Kaltfangvorrichtung für flüssige Metalle und Vorrichtung zur Durchführung dieses Verfahrens
EP0255450B1 (de) Vorrichtung zur Gasschützung eines flüssigen Metallgiessstrahls
WO2008080853A2 (fr) Procede et dispositif de mise en contact sans melange de deux liquides non miscibles
EP0112771B1 (de) Verfahren zur Konditionierung von Abfällen die aus radioaktiven metallischen Partikeln bestehen, z.B. aus Auflösungsstauben zerstrahlter Kernbrennstoffe
CA1139970A (fr) Procede et installation de fabrication de poudre metallique a partir d'un metal ou alliage en fusion
EP0125173B1 (de) Verfahren zur Herstellung erstarrter Metallkörper aus der Schmelze eines Metalls
US5298196A (en) Method and apparatus for extracting tritium and preparing radioactive waste for disposal
EP2700078B1 (de) Vorrichtung und verfahren zum entfernen von tritium
FR2548820A1 (fr) Procede pour remplir des recipients metalliques d'une masse vitreuse fondue radioactive et dispositif de reception d'une masse vitreuse fondue radioactive
FR2705103A1 (fr) Procédé et installation pour le traitement par thermolyse sous vide de produits solides, avec séparation et récupération en continu d'une fraction liquide de ces produits.
BE1006163A4 (fr) Procede de traitement thermique d'objets metalliques sous atmosphere de protection.
EP0028569B1 (de) Verfahren zum Spülen einer Metallschmelze durch Einblasen von Gas
CA2093788C (fr) Procede d'extraction du zinc present dans la fonte liquide, moyens en vue de la mise en oeuvre du procede et produits ainsi obtenus
FR2852608A1 (fr) Procede et installation de recuperation du zinc contenu dans un bain de fonte liquide
US2474979A (en) Process for the extraction of tin from iron alloys
CH518235A (fr) Procédé et dispositif de purification isotopique de l'eau lourde
EP0404685B1 (de) Verfahren und Anlage zur Trennung der Bestandteile einer Legierung
BE1005461A3 (fr) Procede et installation d'affinage de ferromanganese carbure.
WO2020245542A1 (fr) Dispositif pour pieger l'hydrogene
FR2816529A1 (fr) Procede de traitement de residus d'incineration et installation pour la mise en oeuvre d'un tel procede
EP0877827A1 (de) Verfahren und vorrichtung zum behandeln von pulvermaterial
FR2476370A1 (fr) Procede de captage de dechets gazeux radioactifs

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE CH DE GB IT LI LU NL SE

17P Request for examination filed

Effective date: 19870509

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: COMMISSARIAT A L'ENERGIE ATOMIQUE

17Q First examination report despatched

Effective date: 19881213

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE CH DE GB IT LI LU NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Effective date: 19900523

REF Corresponds to:

Ref document number: 3671563

Country of ref document: DE

Date of ref document: 19900628

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19900630

ITF It: translation for a ep patent filed
GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)
NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19910610

Year of fee payment: 6

ITTA It: last paid annual fee
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Effective date: 19920630

Ref country code: CH

Effective date: 19920630

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19930608

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Effective date: 19940604

EUG Se: european patent has lapsed

Ref document number: 86401184.6

Effective date: 19950110

EUG Se: european patent has lapsed

Ref document number: 86401184.6

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: BE

Payment date: 19950607

Year of fee payment: 10

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Effective date: 19960630

BERE Be: lapsed

Owner name: COMMISSARIAT A L'ENERGIE ATOMIQUE

Effective date: 19960630

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20010530

Year of fee payment: 16

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20010615

Year of fee payment: 16

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030101

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20020603

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.

Effective date: 20050603