SE447783B - FUNGICID PREPARATION CONTAINING A TRIAZOLIC COMPOUND AND A BENZIMIDAZOLE - Google Patents
FUNGICID PREPARATION CONTAINING A TRIAZOLIC COMPOUND AND A BENZIMIDAZOLEInfo
- Publication number
- SE447783B SE447783B SE7803184A SE7803184A SE447783B SE 447783 B SE447783 B SE 447783B SE 7803184 A SE7803184 A SE 7803184A SE 7803184 A SE7803184 A SE 7803184A SE 447783 B SE447783 B SE 447783B
- Authority
- SE
- Sweden
- Prior art keywords
- compound
- formula
- benzimidazole
- triazolic
- preparation containing
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Description
447 783 2 Uppfinningen avser även ett förfarande för behand- ling av svampinfektioner på växter, speciellt på säd och vin- druvor, vid vilket man på växterna anbringar en för svamp- bekämpning effektiv mängd av en fungicidal beredning enligt ovan. Beredningen påförs företrädesvis på bladen när som helst efter grödans uppkomst och tills skörden sker, varvid mäng- den och Frekvensen av påföringen bestäms av svampsjukdomens omfattning eller förväntade omfattning. Det är emellertid en speciell Fördel, som erhålles vid användning av de i det föregående angivna kombinationerna, att en lägre frekvens av behandlingen, t.ex. endast en gång varannan eller var tredje vecka, för bekämpning av mjöldaggsinfektioner på druvor, kan effektivt användas, varvid man erhåller en värdefull minskning av arbetskostnaden. The invention also relates to a method for treating fungal infections on plants, in particular on grain and grapes, in which a fungicidal effective amount of a fungicidal preparation as above is applied to the plants. The preparation is preferably applied to the leaves at any time after the crop has grown and until the harvest takes place, the amount and frequency of application being determined by the extent or expected extent of the fungal disease. However, it is a particular advantage obtained when using the above-mentioned combinations that a lower frequency of the treatment, e.g. only once every two or three weeks, for the control of powdery mildew infections on grapes, can be used effectively, obtaining a valuable reduction in labor costs.
Komponenterna av beredníngarna enligt föreliggande uppfinning kan appliceras i följd eller samtidigt på de be- handlade växterna, varvid det senare sättet föredras. För- eningen med formeln I påföres företrädesvis i en mängd av Fä - 500 g/ha vid behandling av druvor, medan föreningar med formeln II företrädesvis påföres i mängder av 100 - 3000 9/ha. Sålunda kan förhållandet mellan föreningar med formeln I och föreningar med formeln II i kombinationer enligt uppfin- ningen ligga i intervallet 5:1 till 1:300, med avseende på vikten. Företrädesvis ligger förhållandet mellan föreningen med formeln I och föreningen med formeln II_ mellan 2:1 och 1:25, varvid 20 - 200 g/ha av föreningen med formeln I på- föres, medan 100 - 500 g/ha av föreningen med formeln Il kan användas.The components of the formulations of the present invention may be applied sequentially or simultaneously to the treated plants, with the latter method being preferred. The compound of formula I is preferably applied in an amount of Fä - 500 g / ha in the treatment of grapes, while compounds of formula II are preferably applied in amounts of 100 - 3000 9 / ha. Thus, the ratio of compounds of formula I to compounds of formula II in combinations according to the invention may be in the range 5: 1 to 1: 300, with respect to weight. Preferably, the ratio of the compound of formula I to the compound of formula II is between 2: 1 and 1:25, 20 to 200 g / ha of the compound of formula I being applied, while 100 to 500 g / ha of the compound of formula II Can be used.
För att förenkla framställning, lagring och transport framställs kombinationerna av föreningarna med formlerna I och II normalt som koncentrat avsedda för utspädning med vat- ten i-den grad som erfordras för att de angivna givorna en- kelt skall erhållas. Dessa koncentrerade beredningar kan inne- hålla 0,5 - 90 viktprocent, företrädesvis 5 - 90 viktprocent, aktiva beståndsdelar tillsammans med minst en inert icke fyto- toxisk bärare. Beredningarna har vanligen formen av ett vät- bart pulver eller puder eller en vattensuspension. Koncentrat- n* 447 783 3 beredningarna är avsedda För lämplig spädning med vatten före användning. Denna bildning av en vattendispersion kan genom- föras i konventionella spruttankar.In order to simplify the preparation, storage and transport, the combinations of the compounds of formulas I and II are normally prepared as concentrates intended for dilution with water to the extent necessary to obtain the indicated yields easily. These concentrated preparations may contain 0.5 to 90% by weight, preferably 5 to 90% by weight, of active ingredients together with at least one inert non-phytotoxic carrier. The formulations are usually in the form of a wettable powder or powder or an aqueous suspension. Concentrates * 447 783 3 preparations are intended for suitable dilution with water before use. This formation of an aqueous dispersion can be carried out in conventional spray tanks.
Vätbara pulver eller puder består av en intim bland- ning av de aktiva beståndsdelarna, minst en inert bärare och lämpliga ytaktiva medel. Den inerta bäraren kan vara attapulgitlera, montmorillonítlera, diatomacéjord, kaolin, glimmar, talk eller renat silikat. Effektiva detergenter är sulfonerade ligniner, naftalensulfonater och kondenserade naftalensulfonater, alkylsuccinater, alkylbensensulfonater, alkylsulfater och nonjoniska ytaktiva medel, t.ex. etylenoxid- addukter av fenol. Vätbara pulver, som ligger inom ramen för uppfinningen, kan ha följande sammansättning: Vätbara pulver Viktprocent Förening med Formel I 0,25 - 10 Förening med Formel Il 10 - 80 Detergent 0 ï 10 Dispergermedel 0. - 10 rm Klumpningshindfande medel o - 10 Inert bärare till 100 Vattensuspensioner och lösningar innehåller de aktiva beståndsdelarna suspenderade eller lösta i vatten eller andra lämpliga lösningsmedel tillsammans med ytaktiva medel, för- tjockningsmedel, frysskyddsmedel eller konserveringsmedel.Wettable powder or powder consists of an intimate mixture of the active ingredients, at least one inert carrier and suitable surfactants. The inert carrier can be attapulgite clay, montmorillonite clay, diatomaceous earth, kaolin, mica, talc or purified silicate. Effective detergents are sulfonated lignins, naphthalene sulfonates and fused naphthalene sulfonates, alkyl succinates, alkyl benzene sulfonates, alkyl sulfates and nonionic surfactants, e.g. ethylene oxide adducts of phenol. Wettable powders, which are within the scope of the invention, may have the following composition: Wettable powders Weight percent Compound of Formula I 0.25 - 10 Compound of Formula II 10 - 80 Detergent 0 ï 10 Dispersant 0. - 10 rm Lump retardant o - 10 Inert carriers to 100 Water suspensions and solutions contain the active ingredients suspended or dissolved in water or other suitable solvents together with surfactants, thickeners, antifreeze or preservatives.
Lämpliga ytaktiva medel kan väljas bland de i samband med vät- bara pulver angivna. Eventuellt använda Förtjockningsmedel väljes vanligen bland cellulosamaterial och naturgummin, medan glykoler normalt användes när ett frysskyddsmedel erfordras.Suitable surfactants can be selected from those indicated in connection with wettable powders. Any thickener used is usually selected from cellulosic materials and natural rubbers, while glycols are normally used when an antifreeze is required.
Konserveringsmedel kan väljas bland många material, t.ex. olika antibakteriella parabener, Fenol, o-klorokresol, fenyl- kvicksilver(lI)nitrat och formaldehyd. Typiska exempel på vattensuspensioner inom ramen För uppfinningen är Följande: 447 783 4 Vattensuspensioner (hållbara) Viktprocent Förening med Formel I 0,1 - 8 Förening med formel II 20 - 52 Detergent(er) Ü - 15 Förtjockningsmedel 0 - 3 Frysskyddsmedel 0 - 20 Konserveringsmedel 0 - 1 Skumdämpare 0 - 0,5 Vatten till 100 De ovan angivna allmänna exemplen anger för fack- mannen vilka slags koncentratkompositíon, som användes enligt uppfinningen, och följande icke begränsande exempel belyser ytterligare beredningarna enligt uppfinningen. I detta exem- pel är föreningen med formeln I betecknad med "CTDB", för- eningen med formeln II(a) med "MBC".Preservatives can be selected from many materials, e.g. various antibacterial parabens, Phenol, o-chlorocresol, phenylmercury (II) nitrate and formaldehyde. Typical examples of aqueous suspensions within the scope of the invention are the following: 447 783 4 Water suspensions (sustainable) Weight percent Compound of Formula I 0.1 - 8 Compound of formula II 20 - 52 Detergent (s) Ü - 15 Thickeners 0 - 3 Antifreeze 0 - 20 Preservatives 0 - 1 Defoamer 0 - 0.5 Water to 100 The general examples given above indicate to the person skilled in the art what kind of concentrate composition was used according to the invention, and the following non-limiting examples further illustrate the preparations according to the invention. In this example, the compound of formula I is designated "CTDB", the compound of formula II (a) is designated "MBC".
Exempel 1 Följande vâtbara pulver framställes: Viktprocent g CTDB 12,0 Mac 60,0 Natriumsalt av kondenserade naftalensulfonsyror 5,0 y Natriumtrideoylsulfat 2,0 _ Kiseldioxíd 5,0 Kaolin till 100,0 I varje exempel blandades de aktiva beståndsdelarna noggrant med de angivna excipienterna i konventionell blandar- utrustning. Blandningen maldes därefter ytterligare i en _ strålkvarn till en storlek av 1 - 10 pm, och slutligen blanda- des blandningen på nytt och avluftades innan den förpackades.Example 1 The following wettable powders are prepared:% by weight g CTDB 12.0 Mac 60.0 Sodium salt of condensed naphthalene sulfonic acids 5.0 y Sodium trideoyl sulphate 2.0 - Silica 5.0 Kaolin to 100.0 the excipients in conventional mixer equipment. The mixture was then further ground in a jet mill to a size of 1-10 microns, and finally the mixture was remixed and deaerated before being packaged.
Exempel 2 __ , Följande vattensuspension framställdes: Viktprocent CTDB 2,5 MBC 50,0 Natriumlaurylsulfat 3,0 Bentonít 3,0 Etylenglykol - 5,0 Formaldehyd 0,2 Vatten till 100 f, 447 783 Bägge de aktiva beståndsdelarna, reducerade i stor- lek på konventionellt sätt, om det är nödvändigt, dispergera- des i vatten innehållande detergentsystemet, konserverings- medel och en del av förtjockningsmedlet. Partikelstorleken för bägge aktiva substanserna reducerades ytterligare genom vätskemalning, återstoden av förtjockningsmedlet tillsattes och fick hydratisera, och produkten späddes med'vatten till önskad volym.Example 2 __, The following aqueous suspension was prepared: Weight percent CTDB 2.5 MBC 50.0 Sodium lauryl sulfate 3.0 Bentonite 3.0 Ethylene glycol - 5.0 Formaldehyde 0.2 Water to 100 f, 447 783 Both the active ingredients, reduced in size play in a conventional manner, if necessary, dispersed in water containing the detergent system, preservatives and part of the thickener. The particle size of both active substances was further reduced by liquid grinding, the residue of the thickener was added and allowed to hydrate, and the product was diluted with water to the desired volume.
Kombinationen av fungiciderna tríadímefon (formel I) och karbendazím (formel II ) testades och befanns uppvisa synergístisk effekt.The combination of the fungicides triadimephone (formula I) and carbendazim (formula II) was tested and found to have a synergistic effect.
Exempel 3 Vattenhaltiga sprayer innehållande 10 och 20 ppm tri~ adimefon och 200 ppm karbendazim framställdes. De anbringades ensamma och i kombination på veteplantor. När plantorna torkat efter behandlíngen.ympades de med uredosporer från rotgvampen Puccinia recondita och placerades sedan i en inkubator i 48 timmar. Efter ínkuberingsperioden placerades plantorna i växt- hus för att låta sjukdomssymtom utvecklas.Example 3 Aqueous sprays containing 10 and 20 ppm triadimefon and 200 ppm carbendazim were prepared. They were applied alone and in combination on wheat plants. When the plants dried after treatment, they were inoculated with uredospores from the root fungus Puccinia recondita and then placed in an incubator for 48 hours. After the incubation period, the plants were placed in greenhouses to allow disease symptoms to develop.
Ett värde på sjukdomsförhindring beräknades genom jämförelse med obehandlade kontrollplantor.A value of disease prevention was calculated by comparison with untreated control plants.
Dos Procent sjukdomsför- ' (ppm) hindríng Kontroll - 0 (45)* tríadimefon 10 19 19 karbendazim 200 37 triadimefon + karbendazím 10 + 200 59 + 200 67 * procent.sjukdomsfall i den obehandlade kontrollen.Dose Percentage of disease ('ppm) inhibition Control - 0 (45) * triadimefon 10 19 19 carbendazim 200 37 triadimefon + carbendazim 10 + 200 59 + 200 67 * per cent.disease cases in the untreated control.
Från värdena, som erhölls när varje fungicid användes ensam var det möjligt att beräkna det teoretiska värdet för blandaíngarnas sjukdomsförhindring, genom den välkända Colby ekvationen (Weeds 15, sid. 20-20 (1967)) och synergistisk effekt uppnåddes genom att de observerade värdena i försöket var högre än de beräknade teoretiska värdena.From the values obtained when each fungicide was used alone, it was possible to calculate the theoretical value of the disease prevention of the mixtures, by the well-known Colby equation (Weeds 15, pp. 20-20 (1967)) and synergistic effect was obtained by observing the values in the experiment was higher than the calculated theoretical values.
Claims (2)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12972/77A GB1596380A (en) | 1977-03-28 | 1977-03-28 | Fungicidal combinations |
Publications (2)
Publication Number | Publication Date |
---|---|
SE7803184L SE7803184L (en) | 1978-09-29 |
SE447783B true SE447783B (en) | 1986-12-15 |
Family
ID=10014480
Family Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7803184A SE447783B (en) | 1977-03-28 | 1978-03-20 | FUNGICID PREPARATION CONTAINING A TRIAZOLIC COMPOUND AND A BENZIMIDAZOLE |
SE8301606A SE454398B (en) | 1977-03-28 | 1983-03-23 | FUNGICID PREPARATION CONTAINING A PYRIMID COMPOUND AND A BENZIMIDAZOLE |
SE8602470A SE8602470L (en) | 1977-03-28 | 1986-05-30 | FUNGICIDE |
SE8703223A SE8703223D0 (en) | 1977-03-28 | 1987-08-19 | FUNGICIDE |
SE8703224A SE8703224D0 (en) | 1977-03-28 | 1987-08-19 | FUNGICIDE |
Family Applications After (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE8301606A SE454398B (en) | 1977-03-28 | 1983-03-23 | FUNGICID PREPARATION CONTAINING A PYRIMID COMPOUND AND A BENZIMIDAZOLE |
SE8602470A SE8602470L (en) | 1977-03-28 | 1986-05-30 | FUNGICIDE |
SE8703223A SE8703223D0 (en) | 1977-03-28 | 1987-08-19 | FUNGICIDE |
SE8703224A SE8703224D0 (en) | 1977-03-28 | 1987-08-19 | FUNGICIDE |
Country Status (34)
Country | Link |
---|---|
JP (1) | JPS53121932A (en) |
AR (2) | AR227124A1 (en) |
AT (1) | AT362195B (en) |
AU (1) | AU515204B2 (en) |
BE (1) | BE865215A (en) |
BG (4) | BG30167A4 (en) |
BR (1) | BR7801746A (en) |
CA (1) | CA1108046A (en) |
CH (1) | CH629363A5 (en) |
CS (4) | CS198289B2 (en) |
DD (1) | DD135031A5 (en) |
DE (2) | DE2858350C2 (en) |
DK (1) | DK149442C (en) |
ES (1) | ES468098A1 (en) |
FR (4) | FR2390096A1 (en) |
GB (1) | GB1596380A (en) |
GR (1) | GR64791B (en) |
HU (2) | HU179506B (en) |
IE (1) | IE46690B1 (en) |
IL (1) | IL54318A (en) |
IN (1) | IN147690B (en) |
IT (1) | IT1105157B (en) |
LU (1) | LU79285A1 (en) |
MX (1) | MX5640E (en) |
NL (1) | NL7803064A (en) |
NO (4) | NO147260C (en) |
NZ (1) | NZ186757A (en) |
PL (4) | PL108903B1 (en) |
PT (1) | PT67801A (en) |
RO (4) | RO78274A (en) |
SE (5) | SE447783B (en) |
SU (1) | SU1409119A3 (en) |
TR (1) | TR20072A (en) |
ZA (1) | ZA781700B (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2560510C2 (en) * | 1975-11-26 | 1989-02-16 | Bayer Ag, 5090 Leverkusen, De | |
IT1143721B (en) * | 1977-12-01 | 1986-10-22 | Sipcam Spa | FUNGICIDAL COMPOSITION FOR THE FIGHT AGAINST PLANT DISEASES |
DE2846038A1 (en) * | 1978-10-23 | 1980-05-08 | Basf Ag | 1,2,4-TRIAZOLE DERIVATIVES, THEIR PRODUCTION AND USE |
DE3208142A1 (en) * | 1982-03-06 | 1983-09-08 | Bayer Ag, 5090 Leverkusen | FUNGICIDAL AGENT |
FR2524261A1 (en) * | 1982-04-01 | 1983-10-07 | Rhone Poulenc Agrochimie | FENARIMOL FUNGICIDE POWDER COMPOSITION |
GB8629360D0 (en) * | 1986-12-09 | 1987-01-21 | Sandoz Ltd | Fungicides |
JPH01167287U (en) * | 1988-05-16 | 1989-11-24 | ||
DE3818903A1 (en) * | 1988-06-03 | 1989-12-14 | Stama Maschinenfabrik Gmbh | DRILLING AND MILLING PLANT |
JPH0274094U (en) * | 1988-11-28 | 1990-06-06 | ||
JPH071190Y2 (en) * | 1989-03-01 | 1995-01-18 | 狭山精密工業株式会社 | Spiral control mechanism in pachinko ball lifting device |
NZ260462A (en) * | 1994-05-05 | 1996-04-26 | Horticulture & Food Res Inst | Tree treatment and composition comprising phosphorous acid, a bioprecursor or a salt thereof and a triazole |
FR2732191B1 (en) * | 1995-03-30 | 2000-12-29 | Rhone Poulenc Agrochimie | ANTIFUNGAL TREATMENT OF BANANA TREES |
GB0811079D0 (en) * | 2008-06-17 | 2008-07-23 | Syngenta Participations Ag | Herbicide formulation |
CN105028419B (en) * | 2012-08-17 | 2017-06-16 | 陕西美邦农药有限公司 | A kind of bactericidal composition containing Fenarimol |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1569940A (en) * | 1967-04-27 | 1969-06-06 | ||
FR2140205B1 (en) | 1971-06-04 | 1977-12-23 | Oreal | |
US3912752A (en) * | 1972-01-11 | 1975-10-14 | Bayer Ag | 1-Substituted-1,2,4-triazoles |
US3868244A (en) | 1972-03-13 | 1975-02-25 | Lilly Co Eli | Plant growth regulation |
US3869456A (en) | 1972-03-13 | 1975-03-04 | Lilly Co Eli | Synthesis of 5-pyrimidinecarbinols |
DE2303757A1 (en) * | 1973-01-26 | 1974-08-15 | Hoechst Ag | Fungicidal wettable powders contg. benzimidazole carbamates - mixed with powdered carrier, penetrating agent, but without emulsifying agents |
DE2354467C3 (en) * | 1973-10-31 | 1981-07-30 | Hoechst Ag, 6000 Frankfurt | Fungicidal dispersions based on benzimidazole methyl carbamate |
DE2456627C2 (en) * | 1973-12-14 | 1984-05-10 | PEPRO - Société pour le Développement et la Vente de Spécialités Chimiques, Lyon | Fungicidal agents based on phosphonic acid esters |
FR2254276B1 (en) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
FR2279331A1 (en) * | 1974-07-24 | 1976-02-20 | Hoechst Ag | Fungicidal wettable powders contg. benzimidazole carbamates - mixed with powdered carrier, penetrating agent, but without emulsifying agents |
DE2560510C2 (en) * | 1975-11-26 | 1989-02-16 | Bayer Ag, 5090 Leverkusen, De |
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1977
- 1977-03-28 GB GB12972/77A patent/GB1596380A/en not_active Expired
-
1978
- 1978-03-15 IT IT48444/78A patent/IT1105157B/en active
- 1978-03-20 MX MX786944U patent/MX5640E/en unknown
- 1978-03-20 SE SE7803184A patent/SE447783B/en not_active IP Right Cessation
- 1978-03-20 FR FR7807978A patent/FR2390096A1/en active Granted
- 1978-03-20 CA CA299,331A patent/CA1108046A/en not_active Expired
- 1978-03-20 IN IN295/CAL/78A patent/IN147690B/en unknown
- 1978-03-20 PT PT67801A patent/PT67801A/en unknown
- 1978-03-21 GR GR55758A patent/GR64791B/en unknown
- 1978-03-21 ES ES468098A patent/ES468098A1/en not_active Expired
- 1978-03-21 DK DK127978A patent/DK149442C/en not_active IP Right Cessation
- 1978-03-21 IL IL54318A patent/IL54318A/en unknown
- 1978-03-21 AR AR271494A patent/AR227124A1/en active
- 1978-03-21 BR BR7801746A patent/BR7801746A/en unknown
- 1978-03-21 CH CH306178A patent/CH629363A5/en not_active IP Right Cessation
- 1978-03-21 DE DE2858350A patent/DE2858350C2/de not_active Expired
- 1978-03-21 RO RO7899324A patent/RO78274A/en unknown
- 1978-03-21 DE DE2812287A patent/DE2812287C2/en not_active Expired
- 1978-03-21 RO RO7893574A patent/RO73042A/en unknown
- 1978-03-21 RO RO7899325A patent/RO78260A/en unknown
- 1978-03-21 RO RO7899323A patent/RO78273A/en unknown
- 1978-03-22 NL NL7803064A patent/NL7803064A/en not_active Application Discontinuation
- 1978-03-22 BG BG041508A patent/BG30167A4/en unknown
- 1978-03-22 NO NO781040A patent/NO147260C/en unknown
- 1978-03-22 LU LU79285A patent/LU79285A1/en unknown
- 1978-03-22 AT AT203678A patent/AT362195B/en not_active IP Right Cessation
- 1978-03-22 BG BG041507A patent/BG30166A4/en unknown
- 1978-03-22 BG BG039128A patent/BG29863A3/en unknown
- 1978-03-22 AU AU34430/78A patent/AU515204B2/en not_active Expired
- 1978-03-22 BE BE6046404A patent/BE865215A/en not_active IP Right Cessation
- 1978-03-22 BG BG041506A patent/BG30165A4/en unknown
- 1978-03-22 NZ NZ186757A patent/NZ186757A/en unknown
- 1978-03-22 DD DD78204345A patent/DD135031A5/en unknown
- 1978-03-23 HU HU78LI322A patent/HU179506B/en unknown
- 1978-03-23 ZA ZA00781700A patent/ZA781700B/en unknown
- 1978-03-23 TR TR20072A patent/TR20072A/en unknown
- 1978-03-23 HU HU812978A patent/HU188701B/en unknown
- 1978-03-23 IE IE588/78A patent/IE46690B1/en unknown
- 1978-03-24 PL PL1978205555A patent/PL108903B1/en unknown
- 1978-03-24 SU SU782594402A patent/SU1409119A3/en active
- 1978-03-24 CS CS781922A patent/CS198289B2/en unknown
- 1978-03-24 CS CS789184A patent/CS198291B2/en unknown
- 1978-03-24 CS CS789185A patent/CS198292B2/en unknown
- 1978-03-24 CS CS789183A patent/CS198290B2/en unknown
- 1978-03-24 PL PL1978216610A patent/PL112146B1/en unknown
- 1978-03-24 PL PL1978216611A patent/PL112622B1/en unknown
- 1978-03-24 JP JP3402678A patent/JPS53121932A/en active Granted
- 1978-03-24 PL PL1978216612A patent/PL112286B1/en unknown
- 1978-09-08 FR FR7825894A patent/FR2390098A1/en active Granted
- 1978-09-08 FR FR7825893A patent/FR2390097A1/en active Granted
- 1978-09-08 FR FR7825895A patent/FR2390099B1/fr not_active Expired
-
1981
- 1981-02-02 AR AR284171A patent/AR225793A1/en active
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1982
- 1982-05-07 NO NO821512A patent/NO148622C/en unknown
- 1982-05-07 NO NO821514A patent/NO148621C/en unknown
- 1982-05-07 NO NO821513A patent/NO148241C/en unknown
-
1983
- 1983-03-23 SE SE8301606A patent/SE454398B/en not_active IP Right Cessation
-
1986
- 1986-05-30 SE SE8602470A patent/SE8602470L/en not_active Application Discontinuation
-
1987
- 1987-08-19 SE SE8703223A patent/SE8703223D0/en not_active Application Discontinuation
- 1987-08-19 SE SE8703224A patent/SE8703224D0/en not_active Application Discontinuation
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