EP0249255A1 - Cycle combiné à turbines à gaz et à vapeur - Google Patents
Cycle combiné à turbines à gaz et à vapeur Download PDFInfo
- Publication number
- EP0249255A1 EP0249255A1 EP87200488A EP87200488A EP0249255A1 EP 0249255 A1 EP0249255 A1 EP 0249255A1 EP 87200488 A EP87200488 A EP 87200488A EP 87200488 A EP87200488 A EP 87200488A EP 0249255 A1 EP0249255 A1 EP 0249255A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- gas
- gas turbine
- combustion
- gasification
- steam
- 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
- 239000007789 gas Substances 0.000 claims abstract description 186
- 238000002309 gasification Methods 0.000 claims abstract description 52
- 238000002485 combustion reaction Methods 0.000 claims abstract description 50
- 238000000034 method Methods 0.000 claims abstract description 44
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000001301 oxygen Substances 0.000 claims abstract description 38
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 38
- 239000002737 fuel gas Substances 0.000 claims abstract description 30
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 25
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 24
- 239000007787 solid Substances 0.000 claims abstract description 18
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims abstract description 6
- 239000003344 environmental pollutant Substances 0.000 claims abstract description 6
- 231100000719 pollutant Toxicity 0.000 claims abstract description 6
- 239000003575 carbonaceous material Substances 0.000 claims abstract description 5
- 239000000920 calcium hydroxide Substances 0.000 claims abstract description 4
- 229910001861 calcium hydroxide Inorganic materials 0.000 claims abstract description 4
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000000292 calcium oxide Substances 0.000 claims abstract description 4
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 claims abstract description 3
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 claims abstract description 3
- 239000000463 material Substances 0.000 claims description 11
- 239000000725 suspension Substances 0.000 claims description 8
- 150000004820 halides Chemical class 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 239000002912 waste gas Substances 0.000 abstract 2
- 239000003546 flue gas Substances 0.000 description 17
- 238000006477 desulfuration reaction Methods 0.000 description 15
- 230000023556 desulfurization Effects 0.000 description 15
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 12
- 239000003245 coal Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000006227 byproduct Substances 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 239000000428 dust Substances 0.000 description 4
- 239000000446 fuel Substances 0.000 description 4
- 239000004449 solid propellant Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000005243 fluidization Methods 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 239000000571 coke Substances 0.000 description 2
- 239000000567 combustion gas Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000002594 sorbent Substances 0.000 description 2
- 150000003464 sulfur compounds Chemical class 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- JGIATAMCQXIDNZ-UHFFFAOYSA-N calcium sulfide Chemical compound [Ca]=S JGIATAMCQXIDNZ-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000003009 desulfurizing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 238000005272 metallurgy Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000002006 petroleum coke Substances 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000019635 sulfation Effects 0.000 description 1
- 238000005670 sulfation reaction Methods 0.000 description 1
- 239000008400 supply water Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
- 239000002916 wood waste Substances 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01K—STEAM ENGINE PLANTS; STEAM ACCUMULATORS; ENGINE PLANTS NOT OTHERWISE PROVIDED FOR; ENGINES USING SPECIAL WORKING FLUIDS OR CYCLES
- F01K23/00—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids
- F01K23/02—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled
- F01K23/06—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled combustion heat from one cycle heating the fluid in another cycle
- F01K23/061—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled combustion heat from one cycle heating the fluid in another cycle with combustion in a fluidised bed
- F01K23/062—Plants characterised by more than one engine delivering power external to the plant, the engines being driven by different fluids the engine cycles being thermally coupled combustion heat from one cycle heating the fluid in another cycle with combustion in a fluidised bed the combustion bed being pressurised
Definitions
- the invention relates to a method for operating a combined gas / steam turbine process, in which the gas turbine process is operated by means of a fuel gas obtained from solid carbon-containing material and then desulfurized, and the steam turbine process is operated by means of the steam obtained in the combustion of the carbon-containing gasification residue and in which the combustion of the carbon-containing gasification residue with oxygen-containing exhaust gases from the gas turbine process takes place.
- coal is supplied to a gasification plant for partial gasification, the gas is freed of pollutants with the aid of a scrubber and then burned in the gas turbine.
- the coke remaining in the partial gasification is burned in the furnace of a steam generator with the oxygen-containing exhaust gases from the gas turbine and the steam is fed to a steam turbine (K. Weinzierl, "Coal gasification to improve efficiency in the power plant” VGB-Krafttechnikstechnik 62 (1982), No. 5, page 365 ff. and Issue 10, page 852 ff.).
- the aforementioned configuration of the gasification stage is associated with a shift of energy from the gas turbine branch into the steam turbine branch, as a result of which - as can be determined thermodynamically - at least a substantial part of the improvement in efficiency is consumed.
- the object of the invention is to provide a combined gas / steam turbine process which does not have the disadvantages of the known, in particular the aforementioned, process (s) and the combustion of solid carbon-containing fuels in an environmentally friendly manner with a high degree of fuel efficiency and power generation with a high degree of efficiency enables.
- the object is achieved by designing the method of the type mentioned at the outset in accordance with the invention in such a way that the fuel gas in a circulating fluidized bed is gasified by 70 to 95% by weight of the carbon content in the carbon-containing material at a temperature of 900 to 1100 * C generated freed from pollutants in the suspension state at 850 to 950'C with calcium hydroxide, calcium oxide and / or calcium carbonate-containing solid and for the most part burns for the operation of the gas turbine to a gas containing at least 5% by volume oxygen of at least 1000 ° C, the combustion of the carbon-containing gasification residues with the production of process steam in a further circulating fluidized bed at a temperature of 800 to 950 ° C. in a near-stoichiometric manner with at least 2 partial streams of oxygen-containing gases supplied at different levels, the majority of which are formed from the gas turbine exhaust gas.
- EP-Al-62 363 It is known from EP-Al-62 363 to carry out gasification from carbon-containing material as a first stage at a pressure of maximum 5 bar and a temperature of 800 to 1100 ° C. by means of oxygen-containing gases in the presence of water vapor in a circulating fluidized bed and to implement 40 to 80% by weight of the carbon contained in the starting material, to remove sulfur compounds from the gas formed at a temperature in the range from 800 to 1000 ° C.
- this concept pursues the goal of helping the industry to equip the production of certain products with energy in various forms, for example as steam for heating purposes, in the form of other high-temperature heat and in the form of clean fuel gases, the combustion of which does not adversely affect the product quality.
- the degree of conversion of the primary energy (eg coal) into the secondary energies fuel gas and process heat should be variable within a wide range in accordance with the respective existing need for one or the other secondary energy.
- solid carbon-containing material means solid fuel at ambient temperature.
- Such materials are, for example, all types of coal including washing piles, coke, petroleum coke, wood waste, peat, oil shale, asphaltenes and refinery residues.
- the principle of the circulating fluidized bed used in the gasification and combustion stage is characterized by the fact that - in contrast to the " classic" fluidized bed, in which a dense phase is separated from the gas space above by a clear density stress - distribution states without a defined boundary layer are available. A leap in density between the dense phase and the dust space above it does not exist; however, the solids concentration within the reactor decreases continuously from bottom to top.
- the desulfurization of the gas produced can take place in any suspension state, e.g. in a pneumatic conveyor or in a Venturi fluidized bed with solids discharge in a downstream separator.
- a circulating fluidized bed can also advantageously be used for desulfurization.
- the gasification process can be carried out below 1000 ° C, e.g. Because fuel gases with a comparatively low calorific value are permissible for the operation of the gas turbine, the desulfurization can also take place in the gasification reactor itself, that is to say in situ.
- the gasification stage can be carried out under any pressure deemed appropriate. It will generally result from the operating data of the gas turbine and will be in the range of 15 - 30 bar. In this case, the highest possible pressures are preferable from thermodynamic conditions.
- the oxygen-containing gas required for the gasification and the water vapor which is generally required should be fed to the fluidized bed reactor of the gasification stage at different heights. It is expedient to supply water vapor predominantly in the form of fluidizing gas and oxygen-containing gas predominantly in the form of secondary gas. Of course, the entry of minor amounts of water vapor can also take place together with the oxygen-containing secondary gas and the entry of minor amounts of oxygen-containing gases together with water vapor as the fluidizing gas.
- the residence time of the gases in the gasification stage - above the Entry point of the carbonaceous material - should be set to 3 to 20 seconds, preferably 10 to 15 seconds. This condition is usually realized by entering the carbonaceous material at a higher level in the gasification stage. On the one hand, this produces a gas which is richer in hydrocarbon and has a correspondingly higher calorific value, and on the other hand ensures that the gas has practically no hydrocarbons condensing in the exhaust system.
- the desulfurization of the fuel gas is expediently carried out using desulfurization agents whose particle size dp50 is 5 to 200 / ⁇ m.
- An average suspension density of 0.1 to 10 kg / m 3 , preferably 1 to 5 kg / m 3 , and an hourly solids circulation rate which is at least 5 times the solids weight in the reactor shaft should be set in the fluidized bed reactor.
- the desulfurization agent dosage should be at least 1.2 to 2.0 times the stoichiometric requirement be. It should be noted that when using dolomite or burnt dolomite, practically only the calcium component reacts with the sulfur compounds. In the case of in-situ desulfurization in the gasification reactor, the effective desulfurization agents introduced with the inorganic constituents of the carbon-containing material must also be taken into account.
- the gas rate during desulfurization is in Depending on the gas pressure set to approx. 1 to 5 m / sec (calculated as empty pipe speed).
- the entire desulfurization agent also required for the combustion stage can be added to the gas desulfurization stage. In this way, the thermal energy required for heating and possibly for deacidification is withdrawn from the gas and thus the gasification and combustion stages are maintained.
- the combustible constituents that are not converted in the gasification stage are considered to be difficult fuels, particularly with regard to environmentally friendly combustion.
- the by-products from gas cleaning are also considered to be very difficult to process. They are advantageously processed in a further circulating fluidized bed.
- the by-products from gas cleaning are removed in an environmentally friendly manner.
- the loaded desulphurization agents coming from the gas cleaning stage in particular insofar as they are in sulfidic form, such as calcium sulfide, are sulfated and thereby converted into landfill-compatible compounds, such as calcium sulfate.
- the heat of oxidation released in the sulfation process is also obtained as steam.
- the other by-products, such as dust from gas dedusting are also converted into environmentally compatible products.
- the combustion takes place in two stages with different amounts of oxygen-containing gases. Their preference lies in a "soft" combustion, with the local one Overheating can be avoided.
- the staged combustion also largely suppresses NO formation.
- the fuel is fed into the zone between the supply points for oxygen-containing fluidizing gas and secondary gas.
- an average suspension density of 15 to 100 kg / m 3 is expediently created above the upper gas supply by adjusting the amounts of fluidization and secondary gas and at least a substantial part of the heat of combustion is removed by means of cooling surfaces located above the upper gas supply in the reactor space.
- the gas velocities prevailing in the fluidized bed reactor above the secondary gas supply are usually above 5 m / s at normal pressure and can be up to 15 m / s, and the ratio of the diameter to the height of the fluidized bed reactor should be chosen such that gas residence times of 0.5 to 8 , 0 s, preferably 1 to 4 s, are obtained.
- any gas which does not impair the nature of the exhaust gas can be used as the fluidizing gas.
- Inert gases such as recirculated flue gas (exhaust gas), nitrogen and water vapor are also suitable.
- exhaust gas recirculated flue gas
- nitrogen and water vapor are also suitable.
- oxygen-containing gas it is particularly advantageous to use oxygen-containing gas as the fluidizing gas.
- a plurality of supply openings for secondary gas are advantageous within each entry level.
- Another expedient embodiment of the combustion process consists in creating an average suspension density of 10 to 40 kg / m 3 above the upper gas supply by adjusting the amounts of fluidization and secondary gas, removing hot solids from the circulating fluidized bed and in the fluidized state by direct and indirect heat exchange cool and return at least a partial flow of cooled solid into the circulating fluidized bed.
- the temperature can be kept constant practically without changing the prevailing in the fluidized bed reactor Achieve operating conditions, i.e. without changing the suspension density, among other things, only by controlled return of the cooled solid.
- the recirculation rate is more or less high.
- the combustion temperatures can be set at will from very low temperatures, which are close above the ignition limit, to very high temperatures, which are limited, for example, by softening the combustion residues. They can be between 650 and 950 ° C.
- the output in steam generation can be increased - without interfering with the gasification stage - if the combustion stage is additionally fed with carbon-containing material.
- the possibility of the separate addition of solid carbon-containing material into the combustion stage allows, especially in the start-up phase, the start of steam turbine operation, regardless of the gasification residue of the gasification stage,
- air as an oxygen-containing gas
- air enriched with oxygen or technically pure oxygen can also be used.
- air enriched with oxygen or technically pure oxygen can also be used.
- Within the combustion stage it is possible to work at normal pressure, but also under pressure, up to about 10 bar.
- Preferred refinements of the invention consist in generating the fuel gas by gasifying at least 80% by weight of the carbon content of the solid carbon-containing material or in cooling the desulfurized fuel gases to a temperature in the range from 350 to 600 ° C. and freeing them from halides.
- the increase in the degree of gasification to at least 80% by weight is generally associated with the advantage that an additionally increased degree of efficiency is achieved.
- the halides are removed dry using calcium oxide or hydroxide, in principle under the same process conditions that are mentioned with regard to the separate desulfurization of the fuel gases.
- the predominant part of the fuel gas produced in the above described manner and purified is burned in a combustion chamber of stoichiometry to produce NO x -deficient flue gases, so that a flue gas is formed with at least 5 vol .-% oxygen. Since the temperature of the flue gas has to be based on the operating conditions of the gas turbine and is usually set to the maximum permissible value under full load operation, the amount of oxygen-containing gases required for combustion will be selected such that this permissible maximum temperature is established. However, the minimum oxygen content of 5% by volume must not be undercut. If necessary, care must be taken to ensure that the fuel gas has a high calorific value.
- the operating temperature of the gas turbine is currently a maximum of 1200 ° C.
- a further advantageous embodiment of the invention provides for the possibly remaining part of the fuel gas to be burned near-stoichiometrically with the formation of low-NO smoke gases, to be cooled and to be fed to a second gas turbine. For the reasons already mentioned, cooling should not go below the permissible gas turbine inlet temperature if possible.
- This embodiment of the invention has a particularly advantageous effect in that a high degree of efficiency can be achieved even in part-load operation.
- the degree of conversion of the primary energy, such as coal, into fuel gas and steam and thus ultimately the overall efficiency of the combined gas / steam turbine process is essentially dependent on the permissible inlet temperature of the flue gas for the Gas turbine determined.
- the ratio of the outputs from the gas turbine to the steam turbine increases with increasing permissible inlet temperature of the flue gases in favor of the gas turbine. This means that as the permissible inlet temperature of the flue gas increases, the extent of gasification increases, and with it that of residue combustion. At gas inlet temperatures of 1200 * C, efficiencies of 45% can be achieved.
- the figure shows a flow diagram of the method according to the invention in a simplified form.
- the fuel gas is generated in the circulating fluidized bed illustrated by (1), which is supplied with oxygen-containing fluidizing gas or with steam or coal via the lines (2 or 3 or 4). It is fed via line (5) to a first heat exchanger (6) and from there to the device (7) for desulfurization. After passing through a further heat exchanger (8), the removal of hydrogen halide, in particular hydrogen chloride, takes place in the device (9) and the dedusting in device (10). The sorbents obtained in the devices (7 and 9), loaded with pollutants of the fuel gas, and the dusts obtained in the device (10) are discharged via the lines (11, 12, 13).
- the fuel gas then passes via line (14) into the combustion chamber (15), which is additionally supplied via line (16) introduced oxygen-containing gas is supplied.
- the flue gas intended for driving the gas turbine (17) is generated in the combustion chamber (15) by superstoichiometric combustion.
- the metering of the oxygen-containing gas is selected such that the optimum temperature is created for the operation of the gas turbine (17).
- Part of the exhaust gas from the gas turbine (17) is fed to the circulating fluidized bed (20) for the combustion of the gasification residue via line (18 and 19) as a fluidizing gas or as a secondary gas. If necessary, fresh oxygen-containing fluidizing gas can be introduced by means of the blower (21).
- the gasification residue is entered via line (22) together with the loaded sorbents and the dusts separated from the fuel gases.
- further desulfurizing agent and, if necessary, additional coal can be fed to the circulating fluidized bed (20) (line 23).
- the steam generated in the steam registers (24) of the circulating fluidized bed (20) is fed via line (25) to the steam turbines (26, 27 and 28) operated under high pressure, medium pressure and low pressure.
- the exhaust gas from the circulating fluidized bed (20) passes through a further heat exchanger (29) into a dedusting system (30) and then into the chimney (31).
- Oxygen-containing flue gas emerging from the gas turbine (17) and not required in the circulating fluidized bed (20) can be fed to a heat exchanger system (33) via line (32) and can be cooled there in a conventional manner. It then also gets into the chimney (31).
- a second gas turbine 34
- the commissioning of which is advantageous particularly in the case of partial load operation. It is preceded by a combustion chamber (35) with a waste heat boiler (36), which can also be designed as a wall-cooled combustion chamber.
- a flue gas obtained by near-stoichiometric combustion.
- the flue gas is generated from fuel gas supplied via line (37) and oxygen-containing gas supplied via line (38).
- the exhaust gas from the gas turbine (34) passes through line (39) into line (32) and, as described above, is utilized.
- 223,000 Nm 3 of gas are generated per hour in the circulating fluidized bed (1).
- 155,000 Nm 3 of air at 350 ° C. and 20 bar are fed in via line (2), 3.9 t of steam at 400 ° C. via line (3) and 70 t of gas coal with a mean particle size of less than 6 mm via line (4) .
- the gas flame coal (35 wt .-% volatile constituents, stated water / ash free) contains and has a calorific value H u of 26 MJ / kg.
- the temperature in the gasification stage is 1050 ° C, the carbon conversion about 85 wt .-%.
- the gas generated is drawn off via line (5), cooled to 900 ° C. in the heat exchanger (6) and desulfurized in the device (7) by adding 5 t / h of CaCO 3 .
- the dates of the gas are
- the gas is then fed to the combustion chamber (15) via line (14) and burned there with 3.6 times the stoichiometric amount of air which is introduced via line (16).
- the resulting flue gas of 1100 ° C is then expanded in the gas turbine (17).
- the exhaust gas from the gas turbine has a temperature of 550 ° C, a pressure of 1.35 bar, an oxygen content of 13 vol.% And an NO x content of 200 mg / Nm 3 .
- Terminal power of the gas turbine (17) assigned generator is 97.MW.
- the gasification residue of 26.7 t / h and the discharges from the devices (7.9 and 10) in a total amount of 5.0 t / h are mixed with a mixing temperature of 955 ° C via line (22) of the circulating fluidized bed (20 ) forwarded. There the combustion takes place with a 25% excess of oxygen at 850 ° C.
- the distribution of the volumes of fluidizing gas to secondary gas takes place in a ratio of 30:70, the fluidizing gas being composed 1/3 of air (blower 21) and 2/3 of gas turbine exhaust gas supplied via line (18) and having a temperature of 300 ° C. .
- the secondary gas for the fluidized bed reactor (20) consists exclusively of gas turbine exhaust gas of 550 ° C (line 19).
- a total of 10% by volume of the gas turbine exhaust gas thus reaches the circulating fluidized bed (20).
- Steam of 100 bar and 535 ° C. is generated in the circulating fluidized bed (20) and is fed to the steam turbine set (26, 27 and 28) via line (25).
- the generator assigned to these steam turbines delivers a net output of 116 MW.
- the exhaust gas from the circulating fluidized bed (20) is cooled in the heat exchanger (29), dedusted in the system (30) and fed to the chimney (31). Due to the favorable combustion conditions, the NOx values are below 175 mg / Nm 3 and the SO x values are below 200 mg / Nm 3 .
- the gas turbine exhaust gas (90% by volume) not used in the combustion process is fed via line (32) to the heat exchanger system (33), where it is cooled to 100 ° C. with preheating of condensate and generation of steam and finally fed to the fireplace (31).
- the G achieved in the present example is 42% efel Kochsgrad, wherein the power proportions of steam and gas turbines, such as about 1: 0.83 behave.
- 40% of the fuel gas generated in the gasification stage (1) is burned with an air excess of 5% in the pressurized combustion chamber (35) to a flue gas of 1100 ° C and expanded in the gas turbine (34).
- the exhaust gas from the gas turbine (34) has a temperature of 550 ° C., a pressure of approx. 1 bar and an oxygen content of approx. 1 vol.%. It is cooled in the heat exchanger system (33) and placed in the chimney (31) at approx. 100'C.
- the terminal power of the generator assigned to the gas turbine (34) is 26 MW.
- the major part of the fuel gas namely the remaining 60%, are fed to the combustion chamber (15) via line (14) and burned with the addition of air of 3.6 times the stoichiometric requirement.
- the flue gas formed at 1100 ° C is then expanded in the gas turbine (17) and cooled to 550 ° C.
- the gas turbine exhaust gas has an oxygen content of 13% by volume and a pressure of 1.35 bar.
- the generator of the gas turbine (17) delivers a terminal power of 58 MW.
- the gasification residue of 26.7 t / h and the discharges from the devices (7, 9 and 10) in a total amount of 5 t / h are fed through line (22) of the circulating fluidized bed (20) and there with at 850 * C. burnt an excess of oxygen of 25%.
- the distribution of the volumes of fluidizing gas to secondary gas is 30:70, the fluidizing gas being composed 1/3 of air (blower 21) and 2/3 of gas turbine exhaust gas supplied via line (18). Its temperature is 300 ° C.
- the secondary gas for the fluidized bed reactor (20) consists exclusively of gas turbine exhaust gas of 550 * C (line 19). A total of 17 vol.% Of the gas turbine exhaust gas reaches the circulating fluidized bed.
- Steam of 100 bar and 535 ° C. is generated in the circulating fluidized bed (20) and is fed to the steam turbine set (26, 27 and 28) via line (25).
- the generator of this steam turbine set delivers a net output of 129 MW.
- Example 1 The exhaust gas from the circulating fluidized bed (20) and the gas turbine exhaust gas not used in the combustion process are carried out as in Example 1.
- the overall efficiency is 42%.
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Combustion & Propulsion (AREA)
- Mechanical Engineering (AREA)
- General Engineering & Computer Science (AREA)
- Engine Equipment That Uses Special Cycles (AREA)
- Fluidized-Bed Combustion And Resonant Combustion (AREA)
- Treating Waste Gases (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT87200488T ATE40182T1 (de) | 1986-04-17 | 1987-03-17 | Kombinierter gas-/dampfturbinen-prozess. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19863612888 DE3612888A1 (de) | 1986-04-17 | 1986-04-17 | Kombinierter gas-/dampfturbinen-prozess |
| DE3612888 | 1986-04-17 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0249255A1 true EP0249255A1 (fr) | 1987-12-16 |
| EP0249255B1 EP0249255B1 (fr) | 1989-01-18 |
Family
ID=6298844
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP87200488A Expired EP0249255B1 (fr) | 1986-04-17 | 1987-03-17 | Cycle combiné à turbines à gaz et à vapeur |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4996836A (fr) |
| EP (1) | EP0249255B1 (fr) |
| JP (1) | JPH0680294B2 (fr) |
| CN (1) | CN1011999B (fr) |
| AT (1) | ATE40182T1 (fr) |
| AU (1) | AU586923B2 (fr) |
| CA (1) | CA1297683C (fr) |
| DE (2) | DE3612888A1 (fr) |
| ES (1) | ES2007290B3 (fr) |
| GR (2) | GR880300114T1 (fr) |
| IN (1) | IN165413B (fr) |
| PT (1) | PT84712B (fr) |
| ZA (1) | ZA872750B (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0495130B1 (fr) * | 1990-08-13 | 1996-10-30 | Asahi Kasei Kogyo Kabushiki Kaisha | Nouvelle resine fluoree et materiau d'enduction a base de celle-ci |
| CN1304734C (zh) * | 2000-06-29 | 2007-03-14 | 福斯特能源公司 | 联合循环发电站以及运行该电站的方法 |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2694870B2 (ja) * | 1988-03-04 | 1997-12-24 | ピーピーエス プロジェクト プロモーション サービス アクティーボラーグ | 熱・電力同時発生プラント |
| JPH0617650B2 (ja) * | 1988-11-14 | 1994-03-09 | バブ日立エンジニアリングサービス株式会社 | ガスタービン排ガス処理方法 |
| DE3907217A1 (de) * | 1989-03-07 | 1990-09-13 | Steinmueller Gmbh L & C | Verfahren zum betreiben eines kombinierten gasturbinen-/dampfturbinen-prozesses |
| SE463776B (sv) * | 1989-05-26 | 1991-01-21 | Nonox Eng Ab | Foerfarande foer att producera elenergi med en acfbc aanggenerator kombinerad med en aangturbinenhet och tvaa gasturbinenheter |
| DE3924615A1 (de) * | 1989-07-26 | 1991-01-31 | Babcock Werke Ag | Kombinierter gas/dampfturbinen-prozess |
| US5078752A (en) * | 1990-03-12 | 1992-01-07 | Northern States Power Company | Coal gas productions coal-based combined cycle power production |
| DE4040699A1 (de) * | 1990-04-27 | 1991-10-31 | Siemens Ag | Kombinierte gas- und dampf-turbinenanlage |
| DE59203618D1 (de) * | 1991-02-26 | 1995-10-19 | Oberoesterr Ferngas | Verfahren und Vorrichtung zum Verbrennen von stückigen, biogenen Brennstoffen. |
| US5190451A (en) * | 1991-03-18 | 1993-03-02 | Combustion Power Company, Inc. | Emission control fluid bed reactor |
| US5236354A (en) * | 1991-03-18 | 1993-08-17 | Combustion Power Company, Inc. | Power plant with efficient emission control for obtaining high turbine inlet temperature |
| GB9111157D0 (en) * | 1991-05-23 | 1991-07-17 | Boc Group Plc | Fluid production method and apparatus |
| JP2544267B2 (ja) * | 1991-12-30 | 1996-10-16 | 川崎重工業株式会社 | 石炭部分ガス化発電方法及び装置 |
| RU95105440A (ru) * | 1992-07-24 | 1997-01-10 | Феаг Ферайнигте Энергиверке АГ (DE) | Способ эксплуатации комбинированной электростанции и устройство для его осуществления |
| US5251433A (en) * | 1992-12-24 | 1993-10-12 | Texaco Inc. | Power generation process |
| GB2274883B (en) * | 1993-02-03 | 1996-09-11 | Europ Gas Turbines Ltd | Electric power generation system |
| US5319924A (en) * | 1993-04-27 | 1994-06-14 | Texaco Inc. | Partial oxidation power system |
| US5375408A (en) * | 1993-07-06 | 1994-12-27 | Foster Wheeler Development Corporation | Combined-cycle power generation system using a coal-fired gasifier |
| US5617715A (en) * | 1994-11-15 | 1997-04-08 | Massachusetts Institute Of Technology | Inverse combined steam-gas turbine cycle for the reduction of emissions of nitrogen oxides from combustion processes using fuels having a high nitrogen content |
| DE19622299C2 (de) * | 1996-05-21 | 2000-10-12 | Ver Energiewerke Ag | Verfahren zum Betrieb einer druckaufgeladenen zirkulierenden Wirbelschichtfeuerung zur Erzeugung eines arbeitsfähigen Gases für die Gasturbine eines Kombikraftwerkes |
| AU2007262669A1 (en) * | 2006-06-23 | 2007-12-27 | Bhp Billiton Innovation Pty Ltd | Power generation |
| AT504863B1 (de) * | 2007-01-15 | 2012-07-15 | Siemens Vai Metals Tech Gmbh | Verfahren und anlage zur erzeugung von elektrischer energie in einem gas- und dampfturbinen (gud) - kraftwerk |
| ITBO20070505A1 (it) * | 2007-07-20 | 2009-01-21 | Samaya S R L | Gruppo per l'abbattimento degli inquinanti dei gas di scarico di macchine a combustione interna |
| JP5215673B2 (ja) * | 2008-01-11 | 2013-06-19 | 三菱重工業株式会社 | 塩化水素供給装置、排ガス処理システム及び塩化水素供給管理システム |
| FR2947824B1 (fr) * | 2009-07-09 | 2011-10-07 | Michel Mazon | Procede et installation de valorisation des polyolefines |
| WO2013010008A1 (fr) * | 2011-07-13 | 2013-01-17 | Conocophillips Company | Procédé et système de production indirecte de vapeur |
| US9352843B2 (en) | 2012-12-31 | 2016-05-31 | United Technologies Corporation | Gas turbine engine having fan rotor driven by turbine exhaust and with a bypass |
| US10421554B2 (en) | 2015-10-05 | 2019-09-24 | United Technologies Corporation | Double propulsor imbedded in aircraft tail with single core engine |
| US10414509B2 (en) | 2017-02-23 | 2019-09-17 | United Technologies Corporation | Propulsor mounting for advanced body aircraft |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU83085A1 (fr) * | 1981-01-23 | 1982-09-10 | Cockerill | Procede de production d'energie au depart de charbon et installation a cet effet |
| DE3338107A1 (de) * | 1982-11-30 | 1984-05-30 | BBC Aktiengesellschaft Brown, Boveri & Cie., Baden, Aargau | Kohlegefeuertes kraftwerk mit wirbelschichtfeuerung |
| US4478039A (en) * | 1980-12-29 | 1984-10-23 | United Technologies Corporation | Utilization of coal in a combined cycle powerplant |
| GB2148734A (en) * | 1983-10-10 | 1985-06-05 | English Electric Co Ltd | Divided fluidised bed |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3086362A (en) * | 1957-11-29 | 1963-04-23 | Richard W Foster-Pegg | Combined steam-gas turbine plant |
| US3986348A (en) * | 1973-04-25 | 1976-10-19 | Switzer Jr George W | Coal-fueled combined cycle power generating system |
| US3991557A (en) * | 1974-07-22 | 1976-11-16 | Donath Ernest E | Process for converting high sulfur coal to low sulfur power plant fuel |
| US4165717A (en) * | 1975-09-05 | 1979-08-28 | Metallgesellschaft Aktiengesellschaft | Process for burning carbonaceous materials |
| DE2624302C2 (de) * | 1976-05-31 | 1987-04-23 | Metallgesellschaft Ag, 6000 Frankfurt | Verfahren zur Durchführung exothermer Prozesse |
| IE51626B1 (en) * | 1980-08-18 | 1987-01-21 | Fluidised Combustion Contract | A fluidised bed furnace and power generating plant including such a furnace |
| JPS5752707A (en) * | 1980-09-16 | 1982-03-29 | Babcock Hitachi Kk | Multi-stage fluidized boiler |
| DE3113993A1 (de) * | 1981-04-07 | 1982-11-11 | Metallgesellschaft Ag, 6000 Frankfurt | Verfahren zur gleichzeitigen erzeugung von brenngas und prozesswaerme aus kohlenstoffhaltigen materialien |
| JPS59215906A (ja) * | 1983-05-20 | 1984-12-05 | Ishikawajima Harima Heavy Ind Co Ltd | 石炭だき二段加熱複合サイクル発電装置 |
-
1986
- 1986-04-17 DE DE19863612888 patent/DE3612888A1/de not_active Withdrawn
- 1986-10-23 IN IN778/CAL/86A patent/IN165413B/en unknown
-
1987
- 1987-03-17 AT AT87200488T patent/ATE40182T1/de not_active IP Right Cessation
- 1987-03-17 ES ES87200488T patent/ES2007290B3/es not_active Expired - Lifetime
- 1987-03-17 EP EP87200488A patent/EP0249255B1/fr not_active Expired
- 1987-03-17 DE DE8787200488T patent/DE3760042D1/de not_active Expired
- 1987-03-25 CA CA000532916A patent/CA1297683C/fr not_active Expired - Lifetime
- 1987-04-13 JP JP62090627A patent/JPH0680294B2/ja not_active Expired - Fee Related
- 1987-04-14 CN CN87102746A patent/CN1011999B/zh not_active Expired
- 1987-04-16 PT PT84712A patent/PT84712B/pt not_active IP Right Cessation
- 1987-04-16 AU AU71749/87A patent/AU586923B2/en not_active Ceased
- 1987-04-16 ZA ZA872750A patent/ZA872750B/xx unknown
-
1989
- 1989-03-08 GR GR88300114T patent/GR880300114T1/el unknown
- 1989-04-19 GR GR89400050T patent/GR3000048T3/el unknown
- 1989-10-18 US US07/423,669 patent/US4996836A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4478039A (en) * | 1980-12-29 | 1984-10-23 | United Technologies Corporation | Utilization of coal in a combined cycle powerplant |
| LU83085A1 (fr) * | 1981-01-23 | 1982-09-10 | Cockerill | Procede de production d'energie au depart de charbon et installation a cet effet |
| DE3338107A1 (de) * | 1982-11-30 | 1984-05-30 | BBC Aktiengesellschaft Brown, Boveri & Cie., Baden, Aargau | Kohlegefeuertes kraftwerk mit wirbelschichtfeuerung |
| GB2148734A (en) * | 1983-10-10 | 1985-06-05 | English Electric Co Ltd | Divided fluidised bed |
Non-Patent Citations (2)
| Title |
|---|
| PATENT ABSTRACTS OF JAPAN, Band 6, Nr. 126 (M-142)[1004], 10. Juli 1982; & JP-A-57 52 707 (BABCOCK HITACHI K.K.) 29-03-1982 * |
| PATENT ABSTRACTS OF JAPAN, Band 9, Nr. 87 (M-372)[1810], 17. April 1985; & JP-A-59 215 906 (ISHIKAWAJIMA HARIMA JUKOGYO K.K.) 05-12-1984 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0495130B1 (fr) * | 1990-08-13 | 1996-10-30 | Asahi Kasei Kogyo Kabushiki Kaisha | Nouvelle resine fluoree et materiau d'enduction a base de celle-ci |
| CN1304734C (zh) * | 2000-06-29 | 2007-03-14 | 福斯特能源公司 | 联合循环发电站以及运行该电站的方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0249255B1 (fr) | 1989-01-18 |
| GR880300114T1 (en) | 1989-03-08 |
| DE3760042D1 (en) | 1989-02-23 |
| PT84712B (pt) | 1989-12-29 |
| CA1297683C (fr) | 1992-03-24 |
| ZA872750B (en) | 1988-12-28 |
| GR3000048T3 (en) | 1990-10-31 |
| PT84712A (de) | 1987-05-01 |
| AU7174987A (en) | 1987-10-22 |
| US4996836A (en) | 1991-03-05 |
| JPH0680294B2 (ja) | 1994-10-12 |
| JPS62251428A (ja) | 1987-11-02 |
| IN165413B (fr) | 1989-10-14 |
| ATE40182T1 (de) | 1989-02-15 |
| CN87102746A (zh) | 1987-11-04 |
| ES2007290B3 (es) | 1990-03-16 |
| DE3612888A1 (de) | 1987-10-29 |
| AU586923B2 (en) | 1989-07-27 |
| CN1011999B (zh) | 1991-03-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0249255B1 (fr) | Cycle combiné à turbines à gaz et à vapeur | |
| EP0441788B1 (fr) | Procede allothermique pour produire un gaz combustible a partir d'ordures menageres ou d'ordures menageres conjointement avec du charbon, et dispositif permettant la mise en uvre du procede | |
| US4602573A (en) | Integrated process for gasifying and combusting a carbonaceous fuel | |
| DE69608140T2 (de) | Methode und vorrichtung zur verwendung von biobrennstoff oder abfallmaterial in der energieproduktion | |
| DE102008054038B3 (de) | Verfahren und Vorrichtung zur Reduzierung von Schadstoffemissionen in Verbrennungsanlagen | |
| DE60015129T2 (de) | System zur erzeugen von elektrischer energie mittels vergasung | |
| DE3014292A1 (de) | Verfahren zur energieerzeugung aus kohlenstoffhaltigen brennstoffen | |
| DE3307848A1 (de) | Verfahren zur nachverbrennung und reinigung von prozessabgasen | |
| EP0062363A1 (fr) | Procédé pour la production simultanée de gaz combustible et d'énergie thermique à partir de matières carbonacées | |
| EP0171097B1 (fr) | Procédé de fabrication d'éponge de fer | |
| EP0413199B1 (fr) | Procédé d'abaissement de la teneur en dioxyde de carbone des gaz résiduaires d'une centrale électrique à turbines à gaz ou à vapeur et centrale électrique l'utilisant | |
| DE2819419A1 (de) | Betriebsverfahren fuer eine kohlevergasungsanlage | |
| DE2539546B2 (de) | Verfahren zur Verbrennung kohlenstoffhaltiger Materialien | |
| DE3517992A1 (de) | Verbrennungsverfahren | |
| DE2624302A1 (de) | Verfahren zur durchfuehrung exothermer prozesse | |
| DE3744565A1 (de) | Leistungserzeugungssystem und verfahren zur verwendung der hydropyrolyse | |
| DE69513106T2 (de) | Erneuerung von Industrie- und Kraftwerkkessel mit einem zirkulierendem Wirbelbett zur Reduzierung von NOx- und SOx-Emissionen | |
| DE69100679T2 (de) | Vergasende Verbrennungsmethode und vergasende Energieerzeugungsmethode. | |
| WO1996021504A1 (fr) | Procede pour la refrigeration et l'epuration des gaz de fumees | |
| EP0410118B1 (fr) | Cycle combiné de turbine à gaz et à vapeur | |
| DE69521248T2 (de) | Kombikraftwerk mit einem Druckreaktor mit zirkulierendem Wirbelbett | |
| DE102009049914B4 (de) | Kohlekraftwerks-Kombiprozess mit integrierter Methanolherstellung | |
| DE19609721A1 (de) | Verfahren zur energetischen Verwertung von Rest- und Abfallstoffen sowie heizwertarmen Brennstoffen in einem Dampfkraftwerk | |
| DE3503603A1 (de) | Feuerungsanlage | |
| DE69313274T2 (de) | Verfahren zum einhalten einer nennbetriebstemperatur der rauchgase in einem kraftwerk mit druckwirbelschichtverbrennung |
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): AT BE CH DE ES FR GB GR IT LI LU NL SE |
|
| 17P | Request for examination filed |
Effective date: 19880130 |
|
| 17Q | First examination report despatched |
Effective date: 19880606 |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE ES FR GB GR IT LI LU NL SE |
|
| REF | Corresponds to: |
Ref document number: 40182 Country of ref document: AT Date of ref document: 19890215 Kind code of ref document: T |
|
| REF | Corresponds to: |
Ref document number: 3760042 Country of ref document: DE Date of ref document: 19890223 |
|
| ET | Fr: translation filed | ||
| ITF | It: translation for a ep patent filed | ||
| GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) | ||
| PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
| PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
| 26 | Opposition filed |
Opponent name: ASEA BROWN BOVERI AG Effective date: 19891005 |
|
| 26 | Opposition filed |
Opponent name: L. & C. STEINMUELLER GMBH Effective date: 19891018 Opponent name: ASEA BROWN BOVERI AG Effective date: 19891005 |
|
| NLR1 | Nl: opposition has been filed with the epo |
Opponent name: ASEA BROWN BOVERI AG |
|
| NLR1 | Nl: opposition has been filed with the epo |
Opponent name: L.& C. STEINMUELLER GMBH |
|
| REG | Reference to a national code |
Ref country code: GR Ref legal event code: FG4A Free format text: 3000048 |
|
| ITTA | It: last paid annual fee | ||
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GR Payment date: 19931223 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19940217 Year of fee payment: 8 |
|
| PLBN | Opposition rejected |
Free format text: ORIGINAL CODE: 0009273 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: OPPOSITION REJECTED |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19940331 Year of fee payment: 8 Ref country code: LU Payment date: 19940331 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19940406 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19940420 Year of fee payment: 8 |
|
| 27O | Opposition rejected |
Effective date: 19940118 |
|
| EPTA | Lu: last paid annual fee | ||
| NLR2 | Nl: decision of opposition | ||
| EAL | Se: european patent in force in sweden |
Ref document number: 87200488.2 |
|
| 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: 19950317 Ref country code: AT Effective date: 19950317 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19950331 Ref country code: CH Effective date: 19950331 Ref country code: BE Effective date: 19950331 |
|
| BERE | Be: lapsed |
Owner name: METALLGESELLSCHAFT A.G. Effective date: 19950331 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY Effective date: 19950930 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19951001 |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL Ref country code: GR Ref legal event code: MM2A Free format text: 3000048 |
|
| NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee |
Effective date: 19951001 |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: IF02 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20030226 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 20030304 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20030311 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20030314 Year of fee payment: 17 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20030320 Year of fee payment: 17 |
|
| 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: 20040317 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040318 Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20040318 |
|
| 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: 20041001 |
|
| EUG | Se: european patent has lapsed | ||
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20040317 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20041130 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
| 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: 20050317 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20040318 |
|
| APAH | Appeal reference modified |
Free format text: ORIGINAL CODE: EPIDOSCREFNO |
|
| PLAB | Opposition data, opponent's data or that of the opponent's representative modified |
Free format text: ORIGINAL CODE: 0009299OPPO |