DE2801787A1 - PEST CONTROL - Google Patents

PEST CONTROL

Info

Publication number
DE2801787A1
DE2801787A1 DE19782801787 DE2801787A DE2801787A1 DE 2801787 A1 DE2801787 A1 DE 2801787A1 DE 19782801787 DE19782801787 DE 19782801787 DE 2801787 A DE2801787 A DE 2801787A DE 2801787 A1 DE2801787 A1 DE 2801787A1
Authority
DE
Germany
Prior art keywords
triazophos
binapacryl
weight ratio
active ingredient
pest control
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.)
Withdrawn
Application number
DE19782801787
Other languages
German (de)
Inventor
Ludwig Dr Emmel
Anna Dr Waltersdorfer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hoechst AG
Original Assignee
Hoechst AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoechst AG filed Critical Hoechst AG
Priority to DE19782801787 priority Critical patent/DE2801787A1/en
Priority to BG7942052A priority patent/BG28696A3/en
Priority to EG25/79A priority patent/EG13763A/en
Priority to DD79210478A priority patent/DD141407A5/en
Priority to ZM4/79A priority patent/ZM479A1/en
Priority to PH22064A priority patent/PH14337A/en
Priority to NZ189371A priority patent/NZ189371A/en
Priority to AR275160A priority patent/AR219961Q/en
Priority to IT19306/79A priority patent/IT1110014B/en
Priority to AT26479A priority patent/ATA26479A/en
Priority to IL56432A priority patent/IL56432A0/en
Priority to MW2/79A priority patent/MW279A1/en
Priority to PT7969082A priority patent/PT69082A/en
Priority to NL7900349A priority patent/NL7900349A/en
Priority to CS79346A priority patent/CS203030B2/en
Priority to ZA79171A priority patent/ZA79171B/en
Priority to BR7900268A priority patent/BR7900268A/en
Priority to PL21282179A priority patent/PL212821A1/en
Priority to AU43397/79A priority patent/AU516996B2/en
Priority to JP229579A priority patent/JPS54101429A/en
Priority to GB791567A priority patent/GB2012587B/en
Priority to DK18279A priority patent/DK18279A/en
Priority to SU792712808A priority patent/SU717989A3/en
Priority to MX797664U priority patent/MX6664E/en
Priority to FR7901077A priority patent/FR2414300A1/en
Priority to OA56712A priority patent/OA06152A/en
Priority to BE0/192941A priority patent/BE873536A/en
Publication of DE2801787A1 publication Critical patent/DE2801787A1/en
Withdrawn legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/16Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic 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)

Description

_ 2αϋ ι_ 2αϋ ι

SCHÄDLINGSBEKÄMPFUNGSMITTELPEST CONTROL PRODUCTS

Gegenstand der Erfindung sind Schädlingsbekämpfungsmittel -insbesondere zur Bekämpfung von Akariden in allen Entwicklungsstadien -die gekennzeichnet sind durch einen Gehalt an 0,0-Diäthyl-(1-phenyl-1,2,4-triazol-3-yl)-thionophosphat (common name: Triazophos) in Kombination mit (2-sec.-Butyl-4,6-dinitrophenyl) -3 ,3-dimethylacrylat (commcn name: Binapacryl).The invention relates to pesticides, in particular for combating acarids in all stages of development -which are characterized by a content of 0,0-diethyl- (1-phenyl-1,2,4-triazol-3-yl) -thionophosphate (common name: Triazophos) in combination with (2-sec-butyl-4,6-dinitrophenyl) -3, 3-dimethyl acrylate (common name: Binapacryl).

Es ist bereits bekannt, daß sowohl Triazophos (I)It is already known that both Triazophos (I)

P - OC9H,- (DT-PS 1 670 876)P - OC 9 H, - (DT-PS 1 670 876)

als auch Binapacryl (II)as well as binapacryl (II)

0-C0-0-C0-

NONO

0-CO-CH=C(CH3)0-CO-CH = C (CH 3 )

(DT-PS 1 099 787)(DT-PS 1 099 787)

akarizide Wirksamkeit besitzen.Have acaricidal activity.

Es wurde nun gefunden, daß Kombinationen aus Triazophos und Binapacryl sich durch eine synergistische Wirksamkeit gegen Akariden und deren Eier - darunter auch Phosphorsäureesterresistente Stämme - auszeichnen. Das Mischungsverhältnis Triazophos : Binapacryl kann dabei im Bereich von 1 : 10 bis 10 : 1 liegen und beträgt vorzugsweise 1 : 1 bis 10 : 1.It has now been found that combinations of Triazophos and Binapacryl are synergistic against Acarids and their eggs - including those resistant to phosphoric acid esters Tribes - distinguish. The mixing ratio Triazophos: Binapacryl can be in the range from 1:10 to 10: 1 and is preferably 1: 1 to 10: 1.

Die erfindungsgemäßen Wirkstoffmischungen können in Form üblicher Zubereitungen wie Emulsionskonzentraten, ÜLV-Lösungen, Dispersionen, Spritzpulvern, Stäuben oder Granulaten formuliertThe active ingredient mixtures according to the invention can be in the form of more conventional ones Preparations such as emulsion concentrates, ÜLV solutions, dispersions, wettable powders, dusts or granules are formulated

909829/0385909829/0385

werden. Der Gesamtwirkstoffgehalt der marktfähigen Formulierungen beträgt dann ca. 10 bis 90 Gew.-?;. Daneben enthalten sie die üblichen Haft-, Netz-, Dispergier-, Füll- und Trägerstoffe. Für den praktischen Einsatz kommen aber auch Tankmischungen aus den einzelnen Wirkstoffkomponenten in entsprechenden Mischungsverhältnissen in Frage.will. The total active ingredient content of the marketable formulations is then approx. 10 to 90 wt .-?;. They also contain the usual adhesives, wetting agents, dispersants, fillers and carriers. However, tank mixes are also sufficient for practical use the individual active ingredient components in appropriate mixing ratios in question.

Emulgierbare Konzentrate werden durch Auflösen der Wirkstoffe in geeigneten organischen Lösungsmitteln erhalten. Als Lösungsmittel hierfür kommen beispielsweise in Frage: Toluol, Xylole, Chlorbenzole und andere höher siedende Aromaten, ferner Benzine oder Paraffinöle, Cyclohexanon, Dime thy lfoi'mamid, Dimethylsulfoxid, Tetrahydrofuran, Dioxan, Diacetonalkohol, Äthylacetat, Isophoron.Emulsifiable concentrates are obtained by dissolving the active ingredients in suitable organic solvents. As a solvent for example: toluene, xylenes, Chlorobenzenes and other higher-boiling aromatics, also gasoline or paraffin oils, cyclohexanone, dimethy lfoi'mamide, dimethyl sulfoxide, Tetrahydrofuran, dioxane, diacetone alcohol, ethyl acetate, isophorone.

Im Falle von "Ultra-Low-Volume" (ULV)-Formulierungen wendet man zweckmäßigerweise hochsiedende Lösungsmittel an, um die Verdunstungsrate beim Versprühen gering zu halten, z. B. höher siedende Paraffine, Ketone oder Estei" sowie evtl. pflanzliche öle.In the case of "Ultra-Low-Volume" (ULV) formulations, use is made expediently high-boiling solvents to reduce the evaporation rate to keep low when spraying, z. B. higher-boiling paraffins, ketones or Estei "as well as possibly vegetable oils.

Als Trägermaterialien für feste Formulierungen kommen vor allem mineralische Stoffe in Frage, z. B. Kieselsäuren und Silikate wie Kieselgur, Kaoline, Tonerden oder Talkum, Kreide oder Kieselkreiden, aber auch Zubereitungen dieser mineralischen Stoffe mit Hilfszusätzen wie Stearaten, Alkyl-, Aryl- oder Alkylarylsulfonaten, Ligninsulfonaten und ähnlichem. Darüber hinaus können weitere Netz-, Dispergier- und Haftstoffe sowie Mahlhilfsmittel der verschiedensten Art zum Zwecke der anwendungsspezifischen Formulierung verwendet werden.As carrier materials for solid formulations, especially mineral substances come into question, eg. B. Silicas and Silicates such as kieselguhr, kaolins, clays or talc, chalk or silica chalks, but also preparations of these mineral ones Substances with auxiliary additives such as stearates, alkyl, aryl or Alkyl aryl sulfonates, lignosulfonates and the like. In addition, other wetting agents, dispersants and adhesives can be used and grinding aids of the most varied types for the purpose of application-specific formulation can be used.

Vor der eigentlichen Anwendung werden die genannten Emulsionskonzentrate, Spritzpulver oder Dispersionen mit einem geeigneten Verdünnungsmittel - gewöhnlich Wasser - weiter verdünnt und so auf eine für praktische Anwendung geeignete Konzentration gebracht. Diese variiert wie üblich mit der Anwendungsart undBefore the actual application, the emulsion concentrates, wettable powders or dispersions mentioned are mixed with a suitable Diluent - usually water - further diluted to a concentration suitable for practical use brought. As usual, this varies with the type of application and

909829/0385909829/0385

-A--A-

den Klimabedingungen, insbesondere Temperatur und Feuchtigkeit, liegt jedoch allgemein, z. B. bei Spritzpulvern, im Bereich von 0,005 bis 1,0 Gew.-% Gesamtwirkstoffanteil.However, the climatic conditions, especially temperature and humidity, is generally, e.g. B. in wettable powders, in the area from 0.005 to 1.0% by weight of total active ingredient.

Die erfindungsgemäßen Schädlingsbekämpfungsmittel besitzen eine ausgezeichnete Wirkung gegen Schadinsekten, gegen Akariden und deren Eier und können in weit geringeren Mengen bzw. Konzentrationen mit Erfolg eingesetzt werden als Schädlingsbekämpfungsmittel, die nur eine der beiden Wirkstoffkomponenten allein enthalten.The pesticides according to the invention have a excellent action against insect pests, acarids and their eggs and can be used in far lower amounts or concentrations Can be used successfully as a pesticide containing only one of the two active ingredient components alone contain.

Darüber hinaus sind die erfindungsgemäßen Mittel auch gegen Phosphorsäureester-resistente Akaridenstämme wirksam.In addition, the agents according to the invention are also against Acarid strains resistant to phosphoric acid ester are effective.

909829/0385909829/0385

FormulierungsbeispieleFormulation examples

1. Emulsionskonzentrat (Gew.-Verhältnis Triazophos : Binapacryl1. Emulsion concentrate (weight ratio Triazophos: Binapacryl

= 10 : 1)= 10: 1)

Binapacryl
Triazophos
Phenylsulfonat Ca Emuisogen EL 400^ Sapogenat T 500® Xylol
Binapacryl
Triazophos
Phenylsulfonat Ca Emuisogen EL 400 ^ Sapogenat T 500® Xylene

4,0 40,04.0 40.0

5,05.0

7,47.4

1,6 42,01.6 42.0

100,0 Gew.-#100.0 wt .- #

2. Emulsionskonzentrat (Gew.-Verhältnis Triazophos : Binapacryl2. Emulsion concentrate (weight ratio Triazophos: Binapacryl

= 1 : 10)= 1: 10)

Binapacryl
Triazophos
Phenylsulfonat Ca Emuisogen EL 360 " Xylol
Binapacryl
Triazophos
Phenylsulfonate Ca Emuisogen EL 360 "Xylene

40,040.0

4,04.0

3,03.0

2,0 51,02.0 51.0

100,0 Gew.-#100.0 wt .- #

y09829/0385y09829 / 0385

Biologische BeispieleBiological examples

Emulsionskonzentrate der Wirkstoffe Triazophos und Binapacryl wurden mit Wasser so verdünnt, daß die in folgenden Beispielen angegebenen Wirkstoffkonzentrationen vorlagen. Diese Wirkstoffpräparationen wurden auf mit Vollpopulationen der jeweiligen Schädlinge stark besetzte Bohnenpflanzen (Phaseolus vulgaris) durch Spritzen bis zum beginnenden Abtropfen gleichmäßig verteilt. Nach Antrocknung der Spritzbeläge wurden die Pflanzen im Gewächshaus aufgestellt. Die Auswertung erfolgte jeweils 8 Tage nach der Behandlung durch mikroskopische Kontrolle.Emulsion concentrates of the active ingredients Triazophos and Binapacryl were diluted with water so that the following examples indicated drug concentrations were available. These active ingredient preparations were on bean plants (Phaseolus vulgaris) heavily populated with full populations of the respective pests evenly distributed by spraying until it begins to drain. After the spray coatings had dried on, the plants became placed in the greenhouse. The evaluation was carried out 8 days after the treatment by microscopic control.

Beispiel 1:Example 1:

Schädlingsstamm: Gemeine Spinnmilbe (Tetranychus urticae),Pest strain: Common spider mite (Tetranychus urticae),

normal sensibel
Gewichtsverhältnis Triazophos : Binapacryl = 1 : 10
normally sensitive
Triazophos: Binapacryl weight ratio = 1:10

WirkstoffActive ingredient Gew.-$ AS in
der Spritzbrühe
Wt .- $ AS in
the spray mixture
Akarizide Wirkung
in io Abtötung
Acaricidal effect
in io mortification
Triazophos
+ Binapacrvl
Triazophos
Binapacryl
Triazophos
+ Binapacrvl
Triazophos
Binapacryl
0,000075
+ 0,00075
0,000075
0,00075
0.000075
+ 0.00075
0.000075
0.00075
92
50
10
92
50
10

909829/0385909829/0385

Beispiel 2:Example 2:

Schädlingsstamm: Gemeine Spinnmilbe (Tetranychus urticae),Pest strain: Common spider mite (Tetranychus urticae),

"Baardse", PE-resistent Gewichtsverhältnis Triazophos : Binapacryl =2:1"Baardse", PE-resistant Triazophos: Binapacryl weight ratio = 2: 1

WirkstoffActive ingredient Gew.-^ AS in
der Spritzbrühe
Wt .- ^ AS in
the spray mixture
Ovizide Wirkung
in $ Abtötung
Ovicidal effect
in $ mortification
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
0,0063
+ 0,0031
0,0063
0,0031
0,0031
+ 0,0016
0,0031
0,0016
0.0063
+ 0.0031
0.0063
0.0031
0.0031
+ 0.0016
0.0031
0.0016
100
0
75
50
0
25
100
0
75
50
0
25th

Beispiel 3:Example 3:

Schädlingsstamm: Gemeine Spinnmilbe (Tetranychus urticae),Pest strain: Common spider mite (Tetranychus urticae),

"Baardse", PE-resistent und selektiert Gewichtsverhältnis Triazophos : Binapacryl = 10 : 1"Baardse", PE-resistant and selected weight ratio Triazophos: Binapacryl = 10: 1

WirkstoffActive ingredient Gew.-# AS in
der Spritzbrühe
Wt .- # AS in
the spray mixture
Ovizide Wirkung
in Abtötung
Ovicidal effect
in i ° death
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
Triazophos
+ Binapacryl
Triazophos
Binapacryl
0,0125
+ 0,00125
0,0125
0,00125
0,0063
+ 0,00063
0,0063
0,00063
0.0125
+ 0.00125
0.0125
0.00125
0.0063
+ 0.00063
0.0063
0.00063
ο ο ο ι ο ο οο ο ο ι ο ο ο
oo to to ι in ηoo to to ι in η

909829/0385909829/0385

Claims (3)

2-BOI737 HOECHST AKTIENGESELLSCHAFT Aktenzeichen: HOE 78/F 007 Datum : 16.01.1978 Dr.TG/jk PATENTANSPRÜCHE2-BOI737 HOECHST AKTIENGESELLSCHAFT File number: HOE 78 / F 007 Date: January 16, 1978 Dr.TG/jk PATENT CLAIMS 1. Schädlingsbekämpfungsmittel, gekennzeichnet durch einen Gehalt an O,O-Diäthyl-(1-phenyl-i,2,4-triazol-3-yl)-thionophosphat (I) in Kombination mit (2-sec.-Butyl-4,6-dinitrophenyl)-3,3-dimethylacrylat (II).1. Pesticides, characterized by a O, O-diethyl (1-phenyl-i, 2,4-triazol-3-yl) thionophosphate content (I) in combination with (2-sec-butyl-4,6-dinitrophenyl) -3,3-dimethylacrylate (II). 2. Schädlingsbekämpfungsmittel gemäß Anspruch 1, dadurch gekennzeichnet, daß das Gewichtsverhältnis der Komponenten I und II 1 : 10 bis 10 : 1 beträgt.2. Pesticide according to claim 1, characterized in that that the weight ratio of components I and II is 1:10 to 10: 1. 3. Schädlingsbekämpfungsmittel gemäß Anspruch 1 und 2, dadurch gekennzeichnet, daß das Gewichtsverhältnis der Komponenten I und II 1 : 1 bis 10 : 1 beträgt.3. Pesticides according to claim 1 and 2, characterized in that the weight ratio of the components I and II is 1: 1 to 10: 1. 9 098 2 9/03859 098 2 9/0385
DE19782801787 1978-01-17 1978-01-17 PEST CONTROL Withdrawn DE2801787A1 (en)

Priority Applications (27)

Application Number Priority Date Filing Date Title
DE19782801787 DE2801787A1 (en) 1978-01-17 1978-01-17 PEST CONTROL
BG7942052A BG28696A3 (en) 1978-01-17 1979-01-12 Composition and method for pest fighting
EG25/79A EG13763A (en) 1978-01-17 1979-01-15 Pesticidal compositions
DD79210478A DD141407A5 (en) 1978-01-17 1979-01-15 SCHAEDLINGSBEKAEMPFUNGSMITTEL
ZM4/79A ZM479A1 (en) 1978-01-17 1979-01-15 Pesticidal compositions
PH22064A PH14337A (en) 1978-01-17 1979-01-15 Synergistic combination of triazophor and binapacryl as pesticides
NZ189371A NZ189371A (en) 1978-01-17 1979-01-15 Synergistic insecticidal composition
AR275160A AR219961Q (en) 1978-01-17 1979-01-15 ANTIPARASITIC PRODUCTS
IT19306/79A IT1110014B (en) 1978-01-17 1979-01-15 Anti-parasitic
AT26479A ATA26479A (en) 1978-01-17 1979-01-15 INSECTICIDES AND ACARICIDES
IL56432A IL56432A0 (en) 1978-01-17 1979-01-15 Pesticidal compositions comprising triazophos together with another active compound
MW2/79A MW279A1 (en) 1978-01-17 1979-01-15 Pesticidal compositions
PT7969082A PT69082A (en) 1978-01-17 1979-01-16 Process for preparing plagicid compositions
NL7900349A NL7900349A (en) 1978-01-17 1979-01-16 PESTICIDES AGAINST HARMFUL ORGANISMS.
CS79346A CS203030B2 (en) 1978-01-17 1979-01-16 Insecticide and acaricide
ZA79171A ZA79171B (en) 1978-01-17 1979-01-16 Pesticidal compositions
BR7900268A BR7900268A (en) 1978-01-17 1979-01-16 PRAGUICIDAL COMPOSITIONS AND THEIR APPLICATION
PL21282179A PL212821A1 (en) 1978-01-17 1979-01-16 PESTICIAL KILLER
AU43397/79A AU516996B2 (en) 1978-01-17 1979-01-16 Pesticidal compositions
JP229579A JPS54101429A (en) 1978-01-17 1979-01-16 Agricultural chemicals
GB791567A GB2012587B (en) 1978-01-17 1979-01-16 Pesticidal compositions
DK18279A DK18279A (en) 1978-01-17 1979-01-16 MEASURES TO COMBAT HARMFUL BODIES AND THE USE OF THE PRODUCT
SU792712808A SU717989A3 (en) 1978-01-17 1979-01-16 Mite control agent
MX797664U MX6664E (en) 1978-01-17 1979-01-17 IMPROVED PROCEDURE FOR PREPARING A PESTICIDE COMPOSITION
FR7901077A FR2414300A1 (en) 1978-01-17 1979-01-17 PESTICIDE PRODUCTS CONTAINING A PHOSPHORIC ESTER AND A DINITRO-PHENOL DERIVATIVE
OA56712A OA06152A (en) 1978-01-17 1979-01-17 Pesticide products containing a phosphoric ester and a dinitro-phenol derivative.
BE0/192941A BE873536A (en) 1978-01-17 1979-01-17 PESTICIDE PRODUCTS CONTAINING A PHOSPHORIC ESTER AND A DINITRO-PHENOL DERIVATIVE

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE19782801787 DE2801787A1 (en) 1978-01-17 1978-01-17 PEST CONTROL

Publications (1)

Publication Number Publication Date
DE2801787A1 true DE2801787A1 (en) 1979-07-19

Family

ID=6029650

Family Applications (1)

Application Number Title Priority Date Filing Date
DE19782801787 Withdrawn DE2801787A1 (en) 1978-01-17 1978-01-17 PEST CONTROL

Country Status (27)

Country Link
JP (1) JPS54101429A (en)
AR (1) AR219961Q (en)
AT (1) ATA26479A (en)
AU (1) AU516996B2 (en)
BE (1) BE873536A (en)
BG (1) BG28696A3 (en)
BR (1) BR7900268A (en)
CS (1) CS203030B2 (en)
DD (1) DD141407A5 (en)
DE (1) DE2801787A1 (en)
DK (1) DK18279A (en)
EG (1) EG13763A (en)
FR (1) FR2414300A1 (en)
GB (1) GB2012587B (en)
IL (1) IL56432A0 (en)
IT (1) IT1110014B (en)
MW (1) MW279A1 (en)
MX (1) MX6664E (en)
NL (1) NL7900349A (en)
NZ (1) NZ189371A (en)
OA (1) OA06152A (en)
PH (1) PH14337A (en)
PL (1) PL212821A1 (en)
PT (1) PT69082A (en)
SU (1) SU717989A3 (en)
ZA (1) ZA79171B (en)
ZM (1) ZM479A1 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2200436A1 (en) * 1971-01-19 1972-08-10 Agripat Sa New esters

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2200436A1 (en) * 1971-01-19 1972-08-10 Agripat Sa New esters

Also Published As

Publication number Publication date
ZM479A1 (en) 1980-08-22
BR7900268A (en) 1979-08-14
MX6664E (en) 1985-10-07
PT69082A (en) 1979-02-01
BE873536A (en) 1979-07-17
GB2012587A (en) 1979-08-01
NL7900349A (en) 1979-07-19
AR219961Q (en) 1980-09-30
NZ189371A (en) 1980-10-24
AU516996B2 (en) 1981-07-02
FR2414300A1 (en) 1979-08-10
ZA79171B (en) 1980-01-30
SU717989A3 (en) 1980-02-25
GB2012587B (en) 1982-06-16
IT1110014B (en) 1985-12-23
OA06152A (en) 1981-06-30
BG28696A3 (en) 1980-06-16
EG13763A (en) 1982-03-31
PH14337A (en) 1981-05-29
IT7919306A0 (en) 1979-01-15
DK18279A (en) 1979-07-18
JPS54101429A (en) 1979-08-10
IL56432A0 (en) 1979-03-12
DD141407A5 (en) 1980-04-30
CS203030B2 (en) 1981-02-27
MW279A1 (en) 1980-03-12
PL212821A1 (en) 1979-09-10
ATA26479A (en) 1981-01-15
AU4339779A (en) 1979-07-26

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