EP0077027B1 - Dieselkraftstoff - Google Patents
Dieselkraftstoff Download PDFInfo
- Publication number
- EP0077027B1 EP0077027B1 EP82109266A EP82109266A EP0077027B1 EP 0077027 B1 EP0077027 B1 EP 0077027B1 EP 82109266 A EP82109266 A EP 82109266A EP 82109266 A EP82109266 A EP 82109266A EP 0077027 B1 EP0077027 B1 EP 0077027B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- tert
- volume
- diesel fuel
- ether
- butyl
- 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
Links
- 239000002283 diesel fuel Substances 0.000 title claims abstract description 41
- 150000001298 alcohols Chemical class 0.000 claims abstract description 10
- 150000002170 ethers Chemical class 0.000 claims abstract description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 15
- 239000000654 additive Substances 0.000 claims description 15
- 230000000996 additive effect Effects 0.000 claims description 10
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 24
- 239000000446 fuel Substances 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 5
- 239000004071 soot Substances 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- WMZNUJPPIPVIOD-UHFFFAOYSA-N 2-[(2-methylpropan-2-yl)oxy]butane Chemical compound CCC(C)OC(C)(C)C WMZNUJPPIPVIOD-UHFFFAOYSA-N 0.000 description 3
- HNFSPSWQNZVCTB-UHFFFAOYSA-N 2-methyl-2-propan-2-yloxypropane Chemical compound CC(C)OC(C)(C)C HNFSPSWQNZVCTB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 238000007792 addition Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000005265 energy consumption Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000010705 motor oil Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- ULOIAOPTGWSNHU-UHFFFAOYSA-N 2-butyl radical Chemical compound C[CH]CC ULOIAOPTGWSNHU-UHFFFAOYSA-N 0.000 description 1
- CQORYVKHJKAITO-UHFFFAOYSA-N 2-methoxy-2,3-dimethylbutane Chemical compound COC(C)(C)C(C)C CQORYVKHJKAITO-UHFFFAOYSA-N 0.000 description 1
- ZIMZJBAYACLZHK-UHFFFAOYSA-N 2-methoxy-2-methylbutane Chemical compound COC(C)(CC)C.COC(C)(C)CC ZIMZJBAYACLZHK-UHFFFAOYSA-N 0.000 description 1
- WYLQOLGJMFRRLX-UHFFFAOYSA-N 2-methoxy-2-methylpentane Chemical compound CCCC(C)(C)OC WYLQOLGJMFRRLX-UHFFFAOYSA-N 0.000 description 1
- JPMDGMWQQNLUIK-UHFFFAOYSA-N 2-methoxy-2-methylpropane Chemical compound COC(C)(C)C.COC(C)(C)C JPMDGMWQQNLUIK-UHFFFAOYSA-N 0.000 description 1
- 239000002028 Biomass Substances 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 150000005218 dimethyl ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/02—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only
- C10L1/026—Liquid carbonaceous fuels essentially based on components consisting of carbon, hydrogen, and oxygen only for compression ignition
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F02—COMBUSTION ENGINES; HOT-GAS OR COMBUSTION-PRODUCT ENGINE PLANTS
- F02B—INTERNAL-COMBUSTION PISTON ENGINES; COMBUSTION ENGINES IN GENERAL
- F02B3/00—Engines characterised by air compression and subsequent fuel addition
- F02B3/06—Engines characterised by air compression and subsequent fuel addition with compression ignition
Definitions
- ether In order to reduce the formation of smoke or soot in diesel engines, it is known to add ether to the diesel fuel, in particular in a mixture with salts of organic acids from metals of the 2nd main group of the periodic table, in particular the barium.
- mono- and di-alkyl ethers of glycols in particular mono- and dimethyl ethers of ethylene glycol, are proposed as ethers.
- These additives have the disadvantage that they are very expensive to produce and their mode of operation as a soot-reducing and exhaust-gas-reducing additive is only slight.
- the pollution of the environment through the emission of cadmium, barium, strontium is to be feared.
- the present invention avoids the difficulties and disadvantages of the known, ether-containing diesel fuels and is distinguished by an improved combustion behavior compared to conventional diesel fuels and thus an increased useful output and a reduced pollutant emissions of the engines operated therewith.
- R I and R2 each represent a methyl, ethyl, n-propyl, 2-propyl, 1-butyl or 2-butyl radical.
- R I and R 2 may be the same or different.
- methyl tert-butyl ether (2-methoxy-2-methyl propane), methyl tert-amyl ether (2-methoxy-2-methyl butane), isopropyl tert-butyl ether (2- (2'- Propoxy) -2-methylpropane), sec-butyl tert-butyl ether (2- (2'-butoxy) -2-methyl propane), methyl tert-2,3-dimethylbutyl ether (2-methoxy -2,3-dimethylbutane) and methyl tert-2-methylpentyl ether (2-methoxy-2-methylpentane).
- Ether mixtures which contain up to 90% by volume of one of the stated ethers are preferred.
- methyl tert-butyl ether is 5-50 vol.%, Of methyl tert.-amyl ether 5-50 vol.%, Of isopropyl tert-butyl ether 5-50 vol.%, Of sec .-Butyl tert-butyl ether 5-50 vol.%, Methyl tert-2,3-dimethyl-butyl ether 5-50 vol.% And methyl tert-2-methylpentyl ether 5-50 vol .%.
- the ethers to be added to the diesel fuel according to the invention can be produced by simple processes from the hydrocarbons which are obtained during the extraction and processing of crude oil and are gaseous or volatile under normal conditions and can be made available in large quantities. It is therefore entirely possible to produce diesel fuel with the additives according to the invention, which consists of up to 40, preferably up to 25% by volume of the ether mixture.
- Common diesel fuel contains cycloparaffins and multinuclear aromatics, which tend to form soot particles during combustion.
- Complying with a prescribed smoke formation number (soot number, smoke unit) requires an excess of air compared to the stoichiometric ratio of fuel / air and thus reduces the maximum energy that can be released per mass of diesel fuel consumed.
- the addition of ether according to the invention greatly reduces the soot formation number, which makes it possible to reduce the excess air. This leads to an increase in the efficiency and thus the useful output of the engine through higher medium pressure.
- the absolute amount of exhaust gas is reduced and pollutant emissions, in particular NO x emissions, are reduced.
- the soot emitted in reduced concentration is characterized by the fact that the extractable carcinogenic components of polycyclic aromatics are significantly reduced.
- the ether mixtures added to the diesel fuel according to the invention can also serve as solubilizers for alcohols, in particular methanol and ethanol. They make it possible to add alcohols with 1 to 4 carbon atoms, e.g. methanol, ethanol, isopropanol, butanol, sec-butanol and tert-butanol, individually or in a mixture, even with low water content, to the diesel fuel, the alcohol content of the fuel being 2 to 40, preferably two se 5 to 25 vol.%. As a result, alcohols obtained from biomass can be used in larger quantities as diesel oil additives.
- solubilizers It is known to add alcohols to diesel fuels using solubilizers.
- solubilizers previously proposed for this purpose are produced by a complex process and are therefore not readily available in the larger quantities required.
- the substances previously considered as solubilizers also lack the property of favorably influencing the combustion behavior of diesel fuels, as is the case with the ethers according to the invention.
- a commercially available diesel fuel with the properties listed in Table 1 was used as the mixture component for the production of the fuels according to the invention and as the basis for the comparative tests.
- the fuels according to Examples 1, 3 and 7 as ignition accelerators were 0.5, 3.5 and 2.0% by weight (based on the fuel) di-sec.-butyl-para-phenyldi amine added.
- the Bosch number (BZ) as a measure of the exhaust ink, and the specific energy consumption were determined using a Daimler-Benz engine 240 D at 4400 min- i and a power of 47.3 kW.
- Table 3 shows the Bosch number and the specific energy consumption of the basic diesel fuel (0) and the mixtures according to Examples 1 to 8.
- Table 3 shows that improvements in the Bosch number as a measure of Russbil up to 62% compared to conventional diesel fuel. Even mixtures whose content of the components according to the invention is only 10% by volume have Bosch numbers which are reduced by up to 38%.
- the NOx values in the exhaust gas were determined with a standard VW Golf D engine with an output of 31.4 kW at 4800 min -1 .
- the results are shown in Table 4. *
- the mixtures according to Examples 1, 2 and 3 contained 1.0, 2.5 and 1.5% by volume (based on the total fuel) of di-sec-butyl-para-phenyldiamine as the ignition accelerator.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Liquid Carbonaceous Fuels (AREA)
- Glass Compositions (AREA)
- Fats And Perfumes (AREA)
- Steroid Compounds (AREA)
- Solid Fuels And Fuel-Associated Substances (AREA)
- Output Control And Ontrol Of Special Type Engine (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT82109266T ATE18919T1 (de) | 1981-10-10 | 1982-10-07 | Dieselkraftstoff. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19813140382 DE3140382A1 (de) | 1981-10-10 | 1981-10-10 | Dieselkraftstoff |
DE3140382 | 1981-10-10 |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0077027A2 EP0077027A2 (de) | 1983-04-20 |
EP0077027A3 EP0077027A3 (en) | 1984-04-25 |
EP0077027B1 true EP0077027B1 (de) | 1986-04-02 |
Family
ID=6143882
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP82109266A Expired EP0077027B1 (de) | 1981-10-10 | 1982-10-07 | Dieselkraftstoff |
Country Status (15)
Country | Link |
---|---|
EP (1) | EP0077027B1 (sv) |
JP (1) | JPS5874789A (sv) |
AT (1) | ATE18919T1 (sv) |
BR (1) | BR8205904A (sv) |
CA (1) | CA1180895A (sv) |
DE (2) | DE3140382A1 (sv) |
DK (1) | DK153225C (sv) |
ES (1) | ES516382A0 (sv) |
FI (1) | FI75592C (sv) |
GR (1) | GR76994B (sv) |
IE (1) | IE53445B1 (sv) |
MX (1) | MX162435A (sv) |
NO (1) | NO160145C (sv) |
PT (1) | PT75662B (sv) |
TR (1) | TR22309A (sv) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58208389A (ja) * | 1982-05-31 | 1983-12-05 | Komatsu Ltd | デイ−ゼルエンジン用アルコ−ルブレンド燃料 |
JPS6357691A (ja) * | 1986-01-21 | 1988-03-12 | ポラ− モレクラ− コ−ポレ−シヨン | 燃料コンデイシヨナ |
JPH01201393A (ja) * | 1988-02-05 | 1989-08-14 | Takara Co Ltd | 玩具用ディーゼルエンジン燃料 |
JPH0393894A (ja) * | 1989-09-06 | 1991-04-18 | Cosmo Sogo Kenkyusho:Kk | 無鉛高性能ガソリン |
US5314511A (en) * | 1992-12-23 | 1994-05-24 | Arco Chemical Technology, L.P. | Diesel fuel |
US5425790A (en) * | 1992-12-23 | 1995-06-20 | Arco Chemical Technology, L.P. | Diesel fuel |
US5308365A (en) * | 1993-08-31 | 1994-05-03 | Arco Chemical Technology, L.P. | Diesel fuel |
WO2001018154A1 (en) * | 1999-09-06 | 2001-03-15 | Agrofuel Ab | Motor fuel for diesel engines |
ATE455834T1 (de) | 2003-06-24 | 2010-02-15 | Biovalue Holding Bv | Verwendung eines oxygenates als additiv zur verringerung der partikelemission in kraftstoffen,insbesondere in dieselkraftstoffen, ottokraftstoffen und rapsmethylester |
ES2894347T3 (es) | 2016-09-21 | 2022-02-14 | Cepsa S A U | Eteres de solcetal, método de producción y usos de los mismos |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR828020A (fr) * | 1936-11-05 | 1938-05-09 | Standard Oil Dev Co | Combustible pour moteur |
FR829581A (fr) * | 1936-12-18 | 1938-06-30 | Standard Oil Dev Co | Combustible pour moteur |
BE786624A (fr) * | 1971-07-31 | 1973-01-24 | Snam Progetti | Procede de reduction de la teneur en oxyde de carbone des gaz d'echappement des moteurs a combustion interne |
EP0020012A1 (en) * | 1979-05-14 | 1980-12-10 | Aeci Ltd | Fuel and method of running an engine |
WO1981000721A1 (en) * | 1979-09-10 | 1981-03-19 | Wer R | Universal fuel for engines |
US4332594A (en) * | 1980-01-22 | 1982-06-01 | Chrysler Corporation | Fuels for internal combustion engines |
DE3163813D1 (en) * | 1980-03-07 | 1984-07-05 | British Petroleum Co Plc | Preparation of a motor spirit blending component |
US4353710A (en) * | 1980-03-26 | 1982-10-12 | Texaco Inc. | Novel method of extending a hydrocarbon fuel heavier than gasoline by adding a methoxy or ethoxy group |
JPS5819389A (ja) * | 1981-07-27 | 1983-02-04 | Reametaru:Kk | A重油の改質方法 |
-
1981
- 1981-10-10 DE DE19813140382 patent/DE3140382A1/de active Granted
-
1982
- 1982-09-03 TR TR6933A patent/TR22309A/xx unknown
- 1982-10-05 GR GR69444A patent/GR76994B/el unknown
- 1982-10-05 CA CA000412887A patent/CA1180895A/en not_active Expired
- 1982-10-07 EP EP82109266A patent/EP0077027B1/de not_active Expired
- 1982-10-07 DE DE8282109266T patent/DE3270279D1/de not_active Expired
- 1982-10-07 AT AT82109266T patent/ATE18919T1/de not_active IP Right Cessation
- 1982-10-08 NO NO823376A patent/NO160145C/no unknown
- 1982-10-08 MX MX194722A patent/MX162435A/es unknown
- 1982-10-08 BR BR8205904A patent/BR8205904A/pt not_active IP Right Cessation
- 1982-10-08 JP JP57176457A patent/JPS5874789A/ja active Granted
- 1982-10-08 IE IE2442/82A patent/IE53445B1/en not_active IP Right Cessation
- 1982-10-08 FI FI823426A patent/FI75592C/sv not_active IP Right Cessation
- 1982-10-08 DK DK446182A patent/DK153225C/da not_active IP Right Cessation
- 1982-10-08 ES ES516382A patent/ES516382A0/es active Granted
- 1982-10-08 PT PT75662A patent/PT75662B/pt not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FI75592B (fi) | 1988-03-31 |
DE3140382A1 (de) | 1983-04-21 |
NO160145B (no) | 1988-12-05 |
IE822442L (en) | 1983-04-10 |
ES8307886A1 (es) | 1983-07-16 |
JPS5874789A (ja) | 1983-05-06 |
TR22309A (tr) | 1987-01-20 |
EP0077027A2 (de) | 1983-04-20 |
ES516382A0 (es) | 1983-07-16 |
DE3270279D1 (en) | 1986-05-07 |
EP0077027A3 (en) | 1984-04-25 |
CA1180895A (en) | 1985-01-15 |
IE53445B1 (en) | 1988-11-09 |
NO160145C (no) | 1989-03-15 |
FI75592C (sv) | 1988-07-11 |
NO823376L (no) | 1983-04-11 |
PT75662A (de) | 1982-11-01 |
JPH036958B2 (sv) | 1991-01-31 |
DK153225B (da) | 1988-06-27 |
BR8205904A (pt) | 1983-09-06 |
DE3140382C2 (sv) | 1990-04-12 |
FI823426A0 (fi) | 1982-10-08 |
DK446182A (da) | 1983-04-11 |
PT75662B (de) | 1985-01-11 |
DK153225C (da) | 1988-12-05 |
FI823426L (fi) | 1983-04-11 |
ATE18919T1 (de) | 1986-04-15 |
MX162435A (es) | 1991-05-10 |
GR76994B (sv) | 1984-09-04 |
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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 |
Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
ITCL | It: translation for ep claims filed |
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