+

WO1994003056A1 - Composition insecticide en aerosol - Google Patents

Composition insecticide en aerosol Download PDF

Info

Publication number
WO1994003056A1
WO1994003056A1 PCT/AU1993/000393 AU9300393W WO9403056A1 WO 1994003056 A1 WO1994003056 A1 WO 1994003056A1 AU 9300393 W AU9300393 W AU 9300393W WO 9403056 A1 WO9403056 A1 WO 9403056A1
Authority
WO
WIPO (PCT)
Prior art keywords
weight
aerosol
propellant
solvent
insecticidal composition
Prior art date
Application number
PCT/AU1993/000393
Other languages
English (en)
Inventor
Ian Alexander Edwin Maccormick
Elizabeth Maccormick
Original Assignee
Ian Alexander Edwin Maccormick
Elizabeth Maccormick
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 Ian Alexander Edwin Maccormick, Elizabeth Maccormick filed Critical Ian Alexander Edwin Maccormick
Priority to AU45524/93A priority Critical patent/AU4552493A/en
Publication of WO1994003056A1 publication Critical patent/WO1994003056A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/30Materials not provided for elsewhere for aerosols
    • 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
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A01N25/04Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
    • A01N25/06Aerosols

Definitions

  • the present invention concerns an aerosol insecticide composition which is particularly suitable for use on aircraft.
  • Many countries have quarantine regulations which require incoming or outgoing aircraft to be treated with an aerosol insecticide. This is to prevent the spread of unwanted insects or of human, veterinary and agricultural vector-born diseases around the world, and into countries like Australia where such diseases can do great harm.
  • Suitable aerosols which are allowed to be used for aircraft disinsection have been recommended by a World Health Organization (WHO) committee.
  • Suitable aerosols include the active ingredients of resmethrin, bioresmethrin, phenothrin and permethrin. These are dispensed from a pressurised container by means of the inclusion of an aerosol propellant.
  • These propellants have traditionally been chlorofluorocarbons (CFCs).
  • Commonly used propellants are 1:1 mixtures of dichlorodifluoromethane (Freon 11), and trichlorofluoromethane (Freon 12).
  • AQIS Australian Quarantine and Inspection Service
  • the present invention therefore provides an aerosol insecticidal composition suitable for use on aircraft, which comprises a dispensing container having aerosol dispensing means, and containing an insecticidal active ingredient, optionally a solvent for the active ingredient, and a propellant gas at a sufficient pressure to dispense the active ingredient from the dispensing means as an aerosol, characterised in that the solvent (if present) is chosen from any one or more of an alcohol, water, or a hydrocarbon such as kerosene, and the propellant is chosen from any one or more of CF-CH j F, DME, C0 2 , or NO,.
  • the solvent if present
  • the propellant is chosen from any one or more of CF-CH j F, DME, C0 2 , or NO,.
  • One preferred embodiment of the invention concerns the aerosol insecticidal composition
  • the solvent if used
  • the propellant is CF-CH.XF-
  • the preferred CF-CH 2 F propellant is HFC 134a (1,1,1,2-tetra-fluoroethane) .
  • the propellant maybe a mixture of DME and either CO- or 0 2 - Otherwise a solvent such as an alcohol and/or water may be used with C0 2 as the propellant. As a further alternative the solvent can be a mixture of alcohol and water together with DME and C0 2 as the propellant.
  • propellants such as CO, or N0 2 can be used in conjunction with CF,CH 2 F.
  • the insecticidal composition should meet WHO standards. These standards can be obtained from WHO Weekly Epide . Rec. (7) 1985 pp.45-47 entitled, "Recommendations on the disinsecting of aircraft". In summary, these recommendations require that the dispenser should discharge the formulation as an aerosol at the rate of 1.0 ⁇ 0.2g per second, and the aerosol produced must comply with various physical requirements; for example, not more than 20% by weight of the aerosol should consist of droplets of a diameter greater than 30 micron and not more than 1% by weight of the aerosol should consist of droplets of a diameter greater than 50 micron.
  • the insecticidal activity of the aerosol produced from its dispenser cannot be inferior to that of the standard reference aerosol having the following formulation: trichlorofluoromethane 42.5% pyrethrum extract (25% pyrethrins) 1.6%
  • the formulation should cause no residual risk to the aircraft structure or operating equipment, and for there to be no risk of fire. Therefore a very low flammability, and a suitable inertness of the composition is highly desirable.
  • the insecticide used should not be dangerous to humans.
  • the insecticide will normally be in a standard dispensing container of the type already used for aircraft. As well as disinsecting the aircraft cabin, the baggage and cargo holds should also be treated. This is often done by the pilot releasing the insecticide in a one-shot container, by remote control, on landing, or before taking off, whereby the insecticide is spread throughout the cargo hold of the aircraft.
  • the insecticide may be released in the passenger cabin either manually by airline stewards spraying the insecticide, or by remote control into the air conditioning system in the aircraft cabin.
  • Suitable insecticides include resmethrin, bioresmethrin, d-phenothrin and/or permethrin (25:75 cis/trans ratio).
  • a suitable mixture of insecticides is permethrin (25:75) in an amount of 2% by weight and d-phenothrin (20:80), also in an amount of 2% by weight. Otherwise each of the preferred insecticides; permethrin (25:75), or d-phenothrin (20:80), may be used alone. These insecticides are available from Roussel Uclaf, for example.
  • the remainder of the contents of the dispensing container will comprise mostly propellant, but may also contain an amount of solvent to dissolve the insecticide, and allow it to be easily dispensed as an aerosol.
  • the presence of a solvent also assists to ensure that all the active ingredient is dispensed from the container into the aircraft, ana to assist the insecticidal activity of the active ingredients.
  • the formulation for cargo holds will normally contain 4% of the two preferred active ingredients, and 8% of solvent.
  • the formulation for use in the passenger compartment will normally containa single active ingredient in an amount of 2%, and 10% of solvent.
  • HCF 134a as the propellant gas with a paraffinic hydrocarbon such as kerosene (“Exxsol”), isoparaffins (“Isopar”) or normal paraffins (“Norpar”) as a solvent; a preferred such solvent being "Exxsol D80” or one selected from Isopar, white spirit and the like.
  • a paraffinic hydrocarbon such as kerosene (“Exxsol”), isoparaffins (“Isopar”) or normal paraffins (“Norpar)
  • solvents are available form Exxon Chemicals, for example.
  • the solvent should be present in an amount of less than about 12% (by weight), ideally about 8% to 10%. If 4% by weight of the composition is active insecticidal ingredients, then the 134a propellant can be present in an amount of about 88% by weight.
  • the container is then pressurised, to a pressure of about 100 psi.
  • the minimum pressure in the can should be at least 60 psi, at normal pressures.
  • the dispensing container is preferably an aluminium monoblock can.
  • the dispensing means can be a one-shot type, whereby on activation the complete contents of the can are expelled. Alternatively, the dispensing means can allow a limited amount of the aerosol to be expelled at a time. A combination of one shot and controllable dispensing is also allowed in accordance with the invention.
  • the can may be lined, if desired, with a lining to prevent corrosion, and leakage.
  • the ingredients may be added to the container in any appropriate order, in accordance with usual practice in producing aerosol products. Any suitable size may be used, but a can of a suitable dimension to be usable in existing release mechanisms that are installed on aircraft is preferred. Cans of 75g and 150g (filled) are suitable, for instance.
  • ingredients may be added to the formulation, in small quantities, if desired.
  • Such ingredients include corrosion inhibitors, pH buffers, perfume, and so on. Suitable such ingredients chosen from the prior art may be used in this instance.
  • the aerosol composition contains 4% active ingredient, an amount of paraffinic hydrocarbon solvent for the active ingredient(s) , such as deodorised kerosene, in an amount of up to about 8% by weight, and as a propellant gas, 134a, (1,1,1,2-tetra-fluoroethane) .
  • the composition may contain 2% of a single active ingredient and 10% of solvent.
  • 134a is a propellant which does not have the environmental dangers previously known for CFCs, and is therefore advantageously used for dispensing aerosols in aircraft.
  • the present invention concerns aerosol compositions for use other than in aircraft, but which advantageously share the same requirements with aerosols used in aircraft.
  • such aerosols can be used in the home as one-shot aerosols for dispensing insecticide throughout a room, when the human inhabitants are not present.
  • the aerosol composition with 134a as the propellant may be used with methoprene as the active insecticidal ingredient, as a one-shot process for treating homes or rooms for dust-mites.
  • personal insecticidal compositions for spraying directly on human skin can utilize the compositions of the present invention.
  • the invention also involves a method of de-insecting aircraft which comprises spraying the cargo holds and/or passenger compartments with an aerosol insecticidal composition referred to above immediately before departure and/or before arrival of said aircraft at an airport.
  • Example la An aerosol formulation is prepared comprising 2% d-phenothrin and 2% permethrin. An amount of 34% DME is added to the formulation, as well as 2% of a corrosion inhibitor. To the container is added water so that the 450 ml can is approximately 40% full of liquid. C0 2 is added to increase the pressure to approximately 100 psi.
  • Example lb The same formulation described in example la is prepared, but instead 20% by weight of DME is added.
  • Example lc 2% each of two different pyrethroid insecticides selected from resmethrin, bioresmethrin, d-phenothrin and permethrin (cis/trans ratio 25/75) are added to a 150 ml monoblock can.
  • a sufficient amount of a mixture of methylated spirits and water is added until the volume comprises about 40% of the can.
  • C0 2 is charged into the container to a pressure of at least 60 psi, and preferably 100 psi.
  • Example 2 An aerosol formulation is prepared comprising 2% by weight of d-phenothrin (trade name “Sumithrin”) and 2% permethrin (25/75 cis/trans ratio). The active ingredients are dissolved in a solvent consisting of deodorised kerosene (trade name “EXXSOL D80"). The solvent constitutes about 8% by weight of the formulation. The dispensing container is then charged with propellant comprising CF 3 CH 2 F (134a) to a pressure of about 80 psi. If desired, a corrosion lining can be incorporated in the dispensing container, to assist with preventing leaks. This aerosol is ideal for use in cargo and baggage holds of aircraft.
  • Example 3 An aerosol formulation is prepared comprising 2% by weight of permethrin (25:75 cis/tra ⁇ s ratio). The active ingredient is dissolved in a solvent consisting of isoparaffins "Isopar”. The solvent constitutes about 10% by weight of the formulation. The dispensing container is then charged with propellant comprising CF 3 CH 2 F (134a) to a pressure of about 80 psi. If desired, a corrosion lining can be incorporated in the dispensing container, to assist with preventing leaks. This formualtion is ideal for spraying in passenger cabins of aircraft.
  • Example 4 Further aerosol formulations were prepared in a similar manner to that described in Example 3, but as the active pesticidal ingredients were used the following: amount (by weight) 2% 2% 2% 2% 2%
  • Example 5 A preferred composition according to the invention was tested using the following procedure. Trials were conducted on domestic legs of a British Airways B747-400s aircraft on a return flight between Sydney and Brisbane. Ten rust red flour beetles (Tribolium castaneum) were placed in plastic cups in which the base had been removed and replaced with insect secure mesh. The cups were placed in wire retainers at various positions in the forward and afterward (aft) holds. Since the cups were open at the top and had a mesh base, air movement past the beetles was relatively unimpeded. Insects were also held in sealed cups inside plastic bags to ensure that extraneous factors were not the cause of the observed insect reaction (controls).
  • Tribolium castaneum Tribolium castaneum
  • the cages were installed before the cargo was loaded and retrieved after the flight which had a duration of about 75 minutes. An attempt was made to maintain the same cage on both flights but loading constraints limited the extent to which this was possible. The cage positions in the forward and afterwards holds on the flights were distributed evenly.
  • the residual insecticide effect of the formulation is an important component in the overall effectiveness of the formulation as it forms an insecticidal active surface to which insects, which were not immobilised by the initial spray, would be exposed during the flight.
  • the currently used formulation discharges at a rate of 4 g/s and it is preferred that the HCF 134a formulation should be discharged at a similar rate.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Materials Engineering (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Toxicology (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Composition insecticide en aérosol pouvant être utilisée dans un avion, se présentant sous forme d'un récipient distributeur pourvu d'un élément distributeur aérosol, et contenant un principe actif insecticide et, éventuellement, un solvant pour le principe actif, ainsi qu'un gaz propulseur à une pression suffisante pour libérer le principe actif à partir de l'élément de distribution sous forme d'un aérosol. La composition se caractérise par le fait que le gaz propulseur est composé d'un ou de plusieurs éléments choisis entre CF3CH2F, DME, CO2 et NO2, et le solvant (s'il est présent) est composé d'hydrocarbure, et/ou d'alcool et/ou d'eau. La composition insecticide en aérosol comprend de préférence un gaz propulseur composé de CF3CH2F, et un solvant composé d'hydrocarbure. L'insecticide comprend idéalement la composition suivante: phénotrine 20:80 2 % en poids; perméthrine 25:75 2 % en poids; solvant à base de pétrole 8 % en poids; gaz propulseur - HFC 134a 88 % en poids ou, selon une variante: phénotrine ou perméthrine 2 % en poids; solvant à base de pétrole 10 % en poids; gaz propulseur - HFC 134a 88 % en poids. Un procédé permettant de désinfecter des avions est également décrit.
PCT/AU1993/000393 1992-07-31 1993-08-02 Composition insecticide en aerosol WO1994003056A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU45524/93A AU4552493A (en) 1992-07-31 1993-08-02 Aerosol insecticide composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPL387592 1992-07-31
AUPL3875 1992-07-31

Publications (1)

Publication Number Publication Date
WO1994003056A1 true WO1994003056A1 (fr) 1994-02-17

Family

ID=3776327

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU1993/000393 WO1994003056A1 (fr) 1992-07-31 1993-08-02 Composition insecticide en aerosol

Country Status (1)

Country Link
WO (1) WO1994003056A1 (fr)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6461591B1 (en) * 1997-02-05 2002-10-08 Jago Research Ag Medical aerosol formulations
US6475467B1 (en) 1998-08-04 2002-11-05 Jago Research Ag Medicinal aerosol formulations
US6585958B1 (en) 1998-07-24 2003-07-01 Jago Research Ag Medicinal aerosol formulations
KR100485412B1 (ko) * 2000-06-13 2005-04-27 전찬민 피복처리용 해충 기피제 조성물
WO2005118605A1 (fr) 2004-05-26 2005-12-15 Exxonmobil Chemical Patents, Inc. Composes metalliques de transition pour la polymerisation d'olefines et l'oligomerisation
EP1249482A4 (fr) * 1999-10-01 2006-04-05 Daizo Co Ltd Composition d'aerosol
EP1661458A4 (fr) * 2003-08-08 2008-01-23 Fumakilla Ltd Aerosol de protection contre les insectes nuisibles
EP2112173A1 (fr) 2008-04-16 2009-10-28 ExxonMobil Chemical Patents Inc. Composés catalytiques et leur utilisation
WO2011079042A2 (fr) 2009-12-24 2011-06-30 Exxonmobil Chemical Patents Inc. Procédé de production d'huiles de base synthétiques inédites
CN102246749A (zh) * 2011-05-17 2011-11-23 范兴华 溶液型水基杀虫剂
AU2012230844B2 (en) * 2011-03-24 2014-10-02 S. C. Johnson & Son, Inc. Pyrethrin based repellant
WO2023081010A1 (fr) 2021-11-05 2023-05-11 Exxonmobil Chemical Patents Inc. Modificateurs de viscosité de polypropylène et huiles lubrifiantes associées

Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2737132A1 (de) * 1976-08-19 1978-02-23 Daikin Ind Ltd Aerosol-zubereitung auf kerosin- basis
US4129603A (en) * 1978-02-07 1978-12-12 Imperial Chemical Industries Limited Manufacture of halogenated compounds
JPS5718776A (en) * 1980-07-10 1982-01-30 Sunstar Inc Propellant for spraying substance in spraying vessel
JPS5973502A (ja) * 1982-10-21 1984-04-25 Fumakiraa Kk エアゾ−ル殺虫剤
JPS6313997A (ja) * 1986-07-03 1988-01-21 矢野技研株式会社 管閉塞装置
US4851595A (en) * 1987-07-07 1989-07-25 E. I. Du Pont De Nemours And Company Liquid phase halogen exchange process for the manufacture of 1,1,1,2-tetrafluoroethane
GB2213725A (en) * 1987-12-15 1989-08-23 Sumitomo Chemical Co Insecticidal aerosol
GB2213726A (en) * 1987-12-15 1989-08-23 Sumitomo Chemical Co Insecticidal aerosol
JPH02149504A (ja) * 1989-06-21 1990-06-08 Earth Chem Corp Ltd ダニ防除方法
JPH02258702A (ja) * 1989-03-31 1990-10-19 Sumitomo Chem Co Ltd 防虫器具および防虫方法
AU7120691A (en) * 1990-02-20 1991-08-22 Atochem Mixtures of dimethyl ether and of 1,1,1,2-tetrafluoroethane and their applications
WO1993009199A1 (fr) * 1991-10-31 1993-05-13 E.I. Du Pont De Nemours And Company Composition de difluoromethane et de tetrafluoroethane

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2737132A1 (de) * 1976-08-19 1978-02-23 Daikin Ind Ltd Aerosol-zubereitung auf kerosin- basis
US4129603A (en) * 1978-02-07 1978-12-12 Imperial Chemical Industries Limited Manufacture of halogenated compounds
JPS5718776A (en) * 1980-07-10 1982-01-30 Sunstar Inc Propellant for spraying substance in spraying vessel
JPS5973502A (ja) * 1982-10-21 1984-04-25 Fumakiraa Kk エアゾ−ル殺虫剤
JPS6313997A (ja) * 1986-07-03 1988-01-21 矢野技研株式会社 管閉塞装置
US4851595A (en) * 1987-07-07 1989-07-25 E. I. Du Pont De Nemours And Company Liquid phase halogen exchange process for the manufacture of 1,1,1,2-tetrafluoroethane
GB2213725A (en) * 1987-12-15 1989-08-23 Sumitomo Chemical Co Insecticidal aerosol
GB2213726A (en) * 1987-12-15 1989-08-23 Sumitomo Chemical Co Insecticidal aerosol
JPH02258702A (ja) * 1989-03-31 1990-10-19 Sumitomo Chem Co Ltd 防虫器具および防虫方法
JPH02149504A (ja) * 1989-06-21 1990-06-08 Earth Chem Corp Ltd ダニ防除方法
AU7120691A (en) * 1990-02-20 1991-08-22 Atochem Mixtures of dimethyl ether and of 1,1,1,2-tetrafluoroethane and their applications
WO1993009199A1 (fr) * 1991-10-31 1993-05-13 E.I. Du Pont De Nemours And Company Composition de difluoromethane et de tetrafluoroethane

Non-Patent Citations (7)

* Cited by examiner, † Cited by third party
Title
"The Merck Index", 10th ed., published 1983, by MERCK & CO (USA), (ed. MARTHA WINDHOLZ), pages 1032 and 1046. *
DERWENT ABSTRACT, Accession No. 84-142657/23, Class C03; & JP,A,59 073 502 (FAMAKILA), 25 April 1984. *
M. JOHNSEN, "The Aerosol Handbook", 2nd ed., published 1982, by WAYNE DORLAND CO (NEW JERSEY), pages 305-372. *
PATENT ABSTRACTS OF JAPAN, C-103, page 120; & JP,A,57 018 776 (SUNSTAR HAMIGAKI), 30 January 1982. *
PATENT ABSTRACTS OF JAPAN, C-649, page 15; & JP,A,63 013 997 (DAINIPPON JOCHUGIKU CO), 31 July 1989. *
PATENT ABSTRACTS OF JAPAN, C-752, page 127; & JP,A,2 149 504 (EARTHCHEM CO), 8 June 1990. *
PATENT ABSTRACTS OF JAPAN, C-794, page 64; & JP,A,2 258 702 (SUMITOMO CHEM CO.), 19 October 1990. *

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6461591B1 (en) * 1997-02-05 2002-10-08 Jago Research Ag Medical aerosol formulations
US6585958B1 (en) 1998-07-24 2003-07-01 Jago Research Ag Medicinal aerosol formulations
US6475467B1 (en) 1998-08-04 2002-11-05 Jago Research Ag Medicinal aerosol formulations
EP1249482A4 (fr) * 1999-10-01 2006-04-05 Daizo Co Ltd Composition d'aerosol
US7226579B1 (en) 1999-10-01 2007-06-05 Daizo Co., Ltd. Aerosol composition
KR100485412B1 (ko) * 2000-06-13 2005-04-27 전찬민 피복처리용 해충 기피제 조성물
EP1661458A4 (fr) * 2003-08-08 2008-01-23 Fumakilla Ltd Aerosol de protection contre les insectes nuisibles
US8568688B2 (en) 2003-08-08 2013-10-29 Fumakilla Limited Aerosol for controlling insect pests
WO2005118605A1 (fr) 2004-05-26 2005-12-15 Exxonmobil Chemical Patents, Inc. Composes metalliques de transition pour la polymerisation d'olefines et l'oligomerisation
EP2112173A1 (fr) 2008-04-16 2009-10-28 ExxonMobil Chemical Patents Inc. Composés catalytiques et leur utilisation
WO2011079042A2 (fr) 2009-12-24 2011-06-30 Exxonmobil Chemical Patents Inc. Procédé de production d'huiles de base synthétiques inédites
AU2012230844B2 (en) * 2011-03-24 2014-10-02 S. C. Johnson & Son, Inc. Pyrethrin based repellant
CN102246749A (zh) * 2011-05-17 2011-11-23 范兴华 溶液型水基杀虫剂
WO2023081010A1 (fr) 2021-11-05 2023-05-11 Exxonmobil Chemical Patents Inc. Modificateurs de viscosité de polypropylène et huiles lubrifiantes associées

Similar Documents

Publication Publication Date Title
WO1994003056A1 (fr) Composition insecticide en aerosol
JPH10508283A (ja) 無能力化組成物およびこれを用いるための装置
KR100396412B1 (ko) 살충활성 유중수 에멀젼
AU2013272528B2 (en) Vermin controlling agent
Borden et al. Evaluation of the push-pull tactic against the mountain pine beetle using verbenone and non-host volatiles in combination with pheromone-baited trees
CA2427909C (fr) Compositions insecticides en aerosol ininflammable
AU2016367395B2 (en) Aerosol product
JP4754472B2 (ja) クモの営巣防止エアゾール剤及びクモの営巣防止方法
JPH07119162B2 (ja) 発泡エアゾール殺虫剤ならびにこれを用いた塗布方法
JPH05238903A (ja) 発泡エアゾール殺虫剤ならびにこれを用いた塗布方法
JPH05286805A (ja) 害虫防除用エアゾール剤組成物
DE10054686A1 (de) Lösch- und Brandschutzmittel
JP4437649B2 (ja) マイクロエマルジョン組成物及びこれを用いたエアゾール剤
Sullivan et al. A comparison of Freon-and water-based insecticidal aerosols for aircraft disinsection
Sullivan et al. Studies on aircraft disinsection at” blocks away”
Bro-Rasmussen Precautionary principle and/or risk assessment
Sullivan et al. Aircraft disinsecting: the effectiveness of Freon-based and water-based phenothrin and permethrin aerosols
DE869135C (de) Einrichtung und Verfahren zum Durchgasen von Aufenthalts- und Lagerraeumen
Sullivan et al. Gas-Propelled Aerosols and Micronized Dusts for Control of Insects in Aircraft. 1. Test Protocol
Sullivan et al. Studies on aircraft disinsection at “blocks away” in tropical areas
Duguet Disinsectization of aircraft: Study made in connexion with the revision of international conventions
JPS60104004A (ja) 低薬害性エアゾ−ル農薬組成物
Schechter et al. Gas-propelled aerosols and micronized dusts for control of insects in aircraft. 2. Pesticide formulations
Ellis Aircraft disinsection: A guide for military & civilian air carriers
Matthews Aircraft disinsection

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AT AU BB BG BR BY CA CH CZ DE DK ES FI GB HU JP KP KR KZ LK LU MG MN MW NL NO NZ PL PT RO RU SD SE SK UA US VN

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG

DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)

Free format text: BY,KZ,NZ,PT,UA,VN,OAPI PATENT(BF,BJ,CF,CG,CI,CM,GA,GN,ML,MR,NE,SN,TD,TG)

121 Ep: the epo has been informed by wipo that ep was designated in this application
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase
NENP Non-entry into the national phase

Ref country code: CA

点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载