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NZ283089A - Ozone-friendly fire extinguishing compositions containing hydrofluorocarbons and acid-scavenging additives and methods - Google Patents

Ozone-friendly fire extinguishing compositions containing hydrofluorocarbons and acid-scavenging additives and methods

Info

Publication number
NZ283089A
NZ283089A NZ283089A NZ28308995A NZ283089A NZ 283089 A NZ283089 A NZ 283089A NZ 283089 A NZ283089 A NZ 283089A NZ 28308995 A NZ28308995 A NZ 28308995A NZ 283089 A NZ283089 A NZ 283089A
Authority
NZ
New Zealand
Prior art keywords
acid
fire
composition
extinguishing
hexafluoropropane
Prior art date
Application number
NZ283089A
Inventor
Mark L Robin
Yuichi Iikubo
Mark A Sweval
Original Assignee
Great Lakes Chemical Corp
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 Great Lakes Chemical Corp filed Critical Great Lakes Chemical Corp
Publication of NZ283089A publication Critical patent/NZ283089A/en

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Classifications

    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62CFIRE-FIGHTING
    • A62C99/00Subject matter not provided for in other groups of this subclass
    • A62C99/0009Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames
    • A62C99/0018Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames using gases or vapours that do not support combustion, e.g. steam, carbon dioxide
    • AHUMAN NECESSITIES
    • A62LIFE-SAVING; FIRE-FIGHTING
    • A62DCHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
    • A62D1/00Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
    • A62D1/0028Liquid extinguishing substances
    • A62D1/0057Polyhaloalkanes

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  • Business, Economics & Management (AREA)
  • Emergency Management (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Fire-Extinguishing Compositions (AREA)

Description

<div class="application article clearfix" id="description"> <p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number £83089 <br><br> New Zealand No. 283089 International No. PCT/US95/03490 <br><br> TO BE ENTERED AFTER ACCEPTANCE AND PUBLICATION <br><br> Priority dates: 28.03.1994; <br><br> Complete Specification Filed: 21.03.1995 <br><br> Classification:^) A62D1/08; A62C13/00,02; A62C35/00 <br><br> Publication date: 24 July 1997 Journal No.: 1418 <br><br> NO DRAWINGS <br><br> NEW ZEALAND PATENTS ACT 1953 <br><br> COMPLETE SPECIFICATION <br><br> Title of Invention: <br><br> Ozone friendly fire extinguishing methods and compositions <br><br> Name, address and nationality of applicant(s) as in international application form: <br><br> GREAT LAKES CHEMICAL CORPORATION, Highway 52 N.W., West Lafayette, Indiana 47906, United States of America <br><br> New Zealand No. 283089 International No. PCT/US95/03490 <br><br> I Priority Date(s): <br><br> Complete Specification Filed: <br><br> Class: <br><br> B.U»»£.3Sjo© <br><br> Publication Date: <br><br> P.O. Journal No: <br><br> NO DRAWINGS <br><br> NEW ZEALAND PATENTS ACT 1953 COMPLETE SPECIFICATION . <br><br> Title of Invention: <br><br> Ozone friendly fire extinguishing methods and compositions <br><br> Name, address and nationality of applicant(s) as in international application form: <br><br> GREAT LAKES CHEMICAL CORPORATION, of Highway 52 N.W., West Lafayette, Indiana 47906, United States of America <br><br> WO 95/26218 <br><br> OZONE FRIENDLY FIRE EXTINGUISHING METHODS AND COMPOSITIONS <br><br> BACKGROUND OF THE INVENTION <br><br> FIELD OF THE INVENTION <br><br> '5 <br><br> The present invention relates to the field of fire extinguishing compositions and methods, and particularly to compositions and methods employing compositions comprised of hydrofluorocarbons and acid scavenging additives. <br><br> DESCRIPTION OF THE PRIOR ART <br><br> 10 The use of certain bromine-containing chemical agents for the extinguishment of fires is common. These agents are in general thought to be effective due to their interference with the normal chain reactions responsible for flame propagation. The most widely accepted mechanism for flame suppression is the 15 radical trap mechanism proposed by Fryburg in Review of <br><br> Literature Pertinent to Fire Extinguishing Agents and to Basic Mechanisms Involved in Their Action. NACA-TN 2102 (1950). It is generally accepted that compounds containing bromine act by interfering with free radical or ionic species in the flame; 20 the presence of fluorine has not been considered as contributing to the fire extinguishing properties of a compound, but will impart stability, reduce toxicity and boiling point, and increase thermal stability. <br><br> Various halogenated hydrocarbons have been employed as fire 25 extinguishants. Prior to 1945, three halogenated <br><br> WO 95/26218 <br><br> PCT/DS95/03490 <br><br> -2- <br><br> extinguislxing agents widely used were carbon tetrachloride, methyl bromide and broniochloromethane. For toxicological reasons, however, the use of these agents has been discontinued. The three fire extinguishing agents presently 5 in common use are bromine-containing compounds, Halon 1301 (CF3Br), Halon 1211 (CF2BrCl) and Ilalon 2402 (BrCF2CF2Br). The effectiveness of these three volatile bromine-containing compounds in extinguishing fires has been described in United States Patent No. 4,014,799, issued to 10 Owens. The National Fire Protection Association (NFPA) publication, the Fire Protection Handbook, Section 18, <br><br> Chapter 2, entitled "Halogenated Agents and Systems" (1985) describes these agents in more detail. <br><br> Although the above named bromine-containing compounds 15 are effective fire fighting agents, those agents containing bromine or chlorine are asserted to be capable of the destruction of the earth's protective ozone layer. For example, Halon 1301 has an Ozone Depletion Potential (ODP) rating of 10, and Halon 1211 has an ODP of 3. As a result of 20 concerns over ozone depletion, the production and sale of these agents after January 1, 1994 is prohibited under international and United States policy. <br><br> The use of hydrofluorocarbons as extinguishing agents has been proposed only recently, for example as described in 25 U.S. Patent 5,124,053 to likubo and Robin. Since the hydrofluorocarbons do not contain bromine or chlorine, the compounds have no effect on the stratospheric ozone layer and their ODP is zero. It has been discovered that certain of these compounds, especially those with a higher ratio of 30 hydrogen to fluorine in the molecule, can decompose to some extent in a fire, producing hydrogen fluoride, HF, which is potentially damaging to personnel and equipment if formed in large quantities. <br><br> It is therefore an object of this invention to provide a 35 method for extinguishing fires as rapidly and effectively as <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> -3- <br><br> the techniques employing presently employed fire extinguishing agents while avoiding the above-named drawbacks. <br><br> It is a further object of this invention to provide an agent for use in a method of the character described that is 5 efficient, economical and environmentally safe with regard to ozone depletion. <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> -4- <br><br> SUMMARY OF THE INVENTION <br><br> Briefly describing one aspect of the present invention there is provided a method of extinguishing a fire that comprises introducing to the fire a fire extinguishing 5 concentration of an extinguishant composition comprising/ and preferably consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive, and maintaining the concentration of the composition until the fire is extinguished. Fire extinguishing compositions comprising, or 10 consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive are also provided. <br><br> It is an object of the present invention to provide an effective method for extinguishing fires. Another object of the present invention is to provide a fire extinguishing 15 method which utilizes particular combinations of hydrofluorocarbons and acid-scavenging additives which are effective at non-toxic levels. <br><br> It is a further object of the present invention to provide a fire extinguishing method which employs compounds 20 that are environmentally safe, having low ozone depletion potential and greenhouse warming effect. <br><br> A further object of the present invention is to provide fire extinguishing compositions comprising blends of hydrofluorocarbons and acid-scavenging additives, which 25 blends are effective and safe in use. <br><br> A further object of the present invention is to provide fire extinguishing compositions which produce reduced amounts of decomposition products compared to other fire extinguishing agents when employed in the extinguishment of 30 fires. <br><br> Further objects of the present invention will be apparent from the description which follows. <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> -5- <br><br> DESCRIPTION OF THE PREFERRED EMBODIMENTS <br><br> For the purpose of promoting an understanding of the principles of the invention, reference will now be made to preferred embodiments of the invention and specific language <br><br> 5 will be used to describe the same. It will nevertheless be understood that no limitation of the scope of the invention is thereby intended, such alterations, further modifications and applications of the principles of the invention as described herein being contemplated as would normally occur <br><br> 10 to one skilled in the art to which the invention relates. <br><br> In accordance with the present invention, it has been found that compositions comprising a hydrofluorocarbon in combination with an acid-scavenging additive provide particularly effective fire extinguishants at concentrations <br><br> 15 safe for use. Because the compositions contain no bromine or chlorine, they have an ozone depletion potential of zero. In addition, the compositions produce less decomposition products than the hydrofluorocarbon analogs, and hence are of reduced toxicity with regard to use in a fire scenario. In a <br><br> 20 related aspect, the invention relates to methods for extinguishing fires which are improved by using these compositions as the fire extinguishing agents. <br><br> The invention is directed to a non-toxic fire extinguishant comprising in combination: <br><br> 25 (a) a hydrofluorocarbon of the formula C H F , <br><br> X y z wherein (y+z) « (2x + 2), and wherein y £ x; and <br><br> (b) one or more substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal 30 halides and urea. The extinguishant compositions may preferably consist essentially of the hydrofluorocarbon and the acid-scavenger(s). <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> Specific hydrofluorocarbons useful in accordance with the present invention include trif luorometliane (CFgll), <br><br> pentaf luoroetliane (CF3CF2H), 1,1,1, 2-tetraf luoroethane (CF3CH2F) ,1,1,1,2,3,3-hexafluoropropane (CF3CIIFCF2H) , 5 1,1,1,3,3,3-hexafluoropropane (CF3CII2CF3), 1,1,2,2,3,3-hexafluoropropane (HCF2CF2CF2H), 1,1,1,2,3,3,3-heptafluoropropane (CF3CHFCF3&gt;, 1,1,1,2,2,3,3-heptafluoropropane (CF3CF2CF2H), <br><br> 1,1,1,2,2,3,3,4, 4-nonafluorobutane (CF3CF2CF2CF2II) , 10 1,1,1,2,3,4,4,4-octafluorobutane (CF3CHFCHFCF3) and 1,1,1,3,3,3-hexafluorobutane (CF3CH2CH2CF3). Other hyclrofluorocarbons within the present invention are <br><br> C3M3F5' C4H3F7' C5HF3FJ]' C5H2F10' <br><br> C5H3F9' C5H4F8' and C5n5F7* <br><br> 15 Specific terpenes useful in accordance with the present invention include cilral, citronellal, limoneiie, dipentene, <br><br> menthol, alpha-pinene, beta-pinene, camphor, vitamin A <br><br> beta-carotene, and isopropenyl-l-methylcyclohexene. The terpenes preferably comprise from about 0.1% to about 10% by <br><br> 20 weight of the extinguishing composition. <br><br> Specific unsaturated oils useful in accordance with the present invention include oleic acid, linoleic acid, palniitoleic acid and vaccenic acid. The unsaturated oils preferably comprise from about 0.1% to about 10% by weight of 25 the extinguishing composition. <br><br> Specific alkali metal halides useful in accordance wiLh the present invention include sodium chloride, potassium chloride, sodium bromide and potassium bromide. The alkali metal lialides preferably comprise from about 0.1% to about 30 10% by weight of the extinguishing composition. <br><br> In accordance with one, embodiment of the present invention, there is provided a method for extinguishing fires which includes the use of a composition comprised of a hydrofluorocarbon and an acid-scavenging additive as a fire <br><br> WO 95/26218 PCT/US95/03490 <br><br> -7- <br><br> extinguishing agent. The compositions may be applied in the variety of methods employed for other halogenated hydrocarbons, including application in a flooding system, portable system or specialized system. The extinguishant is 5 effective in low concentrations, and of course, at high concentrations as well. The concentration employed may depend to some extent on the nature of the fire, the combusting material and the circumstances of application. Generally, application rates preferably range from about 1% 10 to about 25% v/v, and more preferably from about 2% and to about 15% v/v, of the hydrofluorocarbon component in the atmosphere. The acid-scavenging additives comprise from about 0.1% to about 10% by weight of the composition. <br><br> The relative amounts of the hydrofluorocarbon and the 15 acid-scavenging additive are not critical, but rather are dictated by the characteristics desired for the overall composition. For example, in certain applications there may be a greater need for low toxicity, and in other instances, the emphasis may be on cleanliness of the extinguishment. 20 The methods for application of the described fire extinguishing compositions are those known to be useful for the Halon agents. In broad terms, these methods utilize application systems which typically include a supply of agent, a means for releasing or propelling the agent from its 25 container, and one or more discharge nozzles to apply the agent into the hazard or directly onto the burning object. Thus, the agents of this invention may be used in total flooding systems in which the agent is introduced into an enclosed region surrounding a fire at a concentration 30 sufficient to extinguish the fire. In accordance with a total flooding system, equipment or even rooms may be provided with a source of agent and appropriate piping, <br><br> valves and controls so as to automatically and/or manually be introduced at appropriate concentrations in the event that 35 fire should break out. As is known to those skilled in the <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> -8- <br><br> arl, the fire extinguishant may be pressurized with nitrogen or other inert gas at up to about 600 psig at ambient conditions. <br><br> Alternatively, the compositions of the invention may be 5 applied to a fire through the use of conventional portable fire extinguishing equipment. It is usual to increase the pressure in portable fire extinguishers with nitrogen or other inert gases in order to ensure that the agent is completely expelled from the extinguisher. Systems in 10 accordance with this invention may be conveniently pressurized at any desirable pressure up to about 600 psig at ambient conditions. <br><br> The invention will be further described with reference to the following specific Examples. However, it will be 15 understood that these Examples are illustrative and not restrictive in nature. <br><br> EXAMPLE 1 <br><br> A test facility with a total internal volume of 1440 cubic feet was constructed from 2x4 lumber and 3/4" plywood. 20 The enclosure was equipped with two 3 foot by 3 foot windows and two standard doors located on opposite walls. The delivery system consisted of a standard Halon cylinder connected to 1" carbon steel pipe via a stainless steel flexhose, terminating in a standard Halon nozzle located 6 25 inches down from the center of the ceiling. <br><br> A large steel pan was filled with commercial n-heptane and placed in the center of the facility, and the n-heptane was then ignited. Thirty seconds after ignition, the doors to the enclosure were closed and the extinguishing agent 30 released. The enclosure atmosphere was sampled after extinguishment of the fire by pulling a sample of the post-extinguishment atmosphere through a buffer solution contained in a polypropylene bubbler equipped with a 70 micron porous polyethylene frit. Fluoride and HF 35 concentrations were determined employing a fluoride ion <br><br> WO 95/26218 <br><br> PCT/US95/03490 <br><br> -9- <br><br> selective electrode (ISE). The post-extinyuisliment atmosphere was sampled at two locations, one at a height of 6 feet and the second at a height of 2 feet, both sampling points located 2 feet diagonally out from the corner of the 5 enclosure. <br><br> Sixty nine pounds of 1,1,1,2,3,3,3-heptafluoropropane (CF3CHFCF3) was discharged according to the above procedure and resulted in extinguishment of the fire. <br><br> Analysis showed the concentration of HF to be 3535 ppm at the 0 G foot location and 1948 ppm at the 2 foot location. <br><br> EXAMPLE 2 <br><br> The procedure of Example 1 was repeated employing 69 pounds of 1,1,1,2,3,3,3-heptafluoropropane (CF3CHFCF3) to which had been added 1.0 pounds of dipentene (1.4 % by 5 weight). Analysis showed the concentration of HF to be 2403 ppm at the 6 foot location and 1202 ppm at the 2 foot location. <br><br> This example demonstrates the advantageous effect of the addition of a small amount of an acid-scavenging additive to 0 the hydrofluorocarbon. The amount of HF priJuced was reduced by 32% at the 6 foot location and by 38% at the 2 foot location. <br><br> EXAMPLE 3 <br><br> The procedure of Example 1 was repeated employing a 5 small steel pan filled with n-heptane. Analysis of the post-extinguishment atmosphere showed a concentration of HF of 50 ppm at the 6 foot location and 11 ppm at the 2 foot location. <br><br> EXAMPLE 4 <br><br> 0 The procedure of Example 3 was repeated employing 69 <br><br> pounds of 1,1,1,2,3,3,3-heptafluoropropane (CF3CHFCF3) to which had been added 1.0 pounds of limonene (1.4 % by <br><br></p> </div>

Claims (18)

  1. <div class="application article clearfix printTableText" id="claims">
    <p lang="en">
    WO 95/26218<br><br>
    PCT/US95/03490<br><br>
    -10-<br><br>
    weiglit) . Following extinguishment of the fire, analysis showed the concentration of I1F to be 32 ppm at the 6 foot location and 7 ppm at the 2 foot location.<br><br>
    This example demonstrates the advantageous effect of the 5 addition of a small amount of an acid-scavenging additive to the hydrofluorocarbon. The amount of HF produced was reduced by 36% at both locations.<br><br>
    EXAMPLE 5<br><br>
    Testing of the fire suppressing and extinguishing 10 capabilities of 1,1,1,2 , 3, 3 ,3-heptaf luoropropane with eacli of the following acid-scavengers yields similarly advantageous results: citral, citronellal, menthol, alpha-pinene, beta-pinene, camphor, vitamin A beta-carotene, isopoopenyl-l-l-methylcyclohexene, oleic acid, linoleic acid, 15 palutitoleic acid, vaccenic acid, sodium chloride, potassium chloride, sodium bromide and potassium bromide. Desirable results are achieved for combinations of 90% to 99.9% by weiglit of the 1,1,1, 2, 3 , 3, 3-heptaf luoropropane and of 0.1%' to 10.0% of the acid-scavenger. Similarly, suitable results are 20 obtained for fire extinguishant compositions comprising blends of the foregoing acid-scavengers and the various other hydrofluorocarbons defined herein, including for example, trifiuoromethane, pentafluoroethane,<br><br>
    1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3-hexafluoropropane, 25 1,1,1,3,3,3-hexafluoropropane, 1,1,2,2,3,3-hexafluoropropane, 1,1,1,2,2,3,3-heptafluoropropane, 1,1,1,2,2,3,3,4,4-nonafluorobutane, 1,1,1,2,3,4,4,4-octafluorobutane and<br><br>
    1,1,1,3,3,3-hexafluorobutane. The foregoing compositions are 30 effective in both total flooding and portable fire extinguishing systems, and work conventionally with typical, known propellants.<br><br>
    28 3 0 8 9<br><br>
    -ii-<br><br>
    WHAT WE CLAIM IS:<br><br>
    1. A method for extinguishing a fire comprising the steps of:<br><br>
    a. introducing to the fire a fire extinguishing concentration of a composition consisting of in combination:<br><br>
    (i) one or more hydrofluorocarbons of the formula<br><br>
    C II F , wherein (y+z) = (2x + 2), and wherein x y z y ± x; and<br><br>
    (ii) one or more substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal halides and urea; and b. maintaining the concentration of the composition until the fire is extinguished.<br><br>
  2. 2. The method of claim 1 wherein the composition is employed at a level of less than about 25% v/v of the hydrofluorocarbons.<br><br>
  3. 3. The method of claim 1 wherein the extinguishing concentration of the compound is from about 1% to about 15% v/v of the hydrofluorocarbons.<br><br>
  4. 4. The method of claim 1 wherein the composition is introduced by a total flooding system.<br><br>
  5. 5. The method of claim 1 wherein the composition is introduced by a portable extinguishing system.<br><br>
  6. 6. The method of claim 1 wherein the composition contains from about 90 co 99.9 percent by weight hydrofluorocarbon.<br><br>
  7. 7. The' method of claim 1 wherein the composition contains .from about 0.1 to about 10 percent by weiglit of one or more<br><br>
    -12-<br><br>
    28 3 08 9<br><br>
    of the substances selected from the group consisting of terpenes, unsaturated oils, sodium bicarbonate, potassium bicarbonate, monoammonium phosphate, alkali metal halides and urea.<br><br>
  8. 8. The method of claim 1 wherein the composition consists essentially of from about 90% to about 99.9% by weight of said hydrofluorocarbon and from about 0.1% to about 10.0% of said substance.<br><br>
  9. 9. The method of claim 1 wherein the composition consists of aboui Jo.6% by weight hydrofluorocarbon and about 1.4% by weight of said substance.<br><br>
  10. 10. The method of claim 1 in which said substance consists of a terpene selected from the group consisting of citral, citronellal, limonene, dipentene, menthol, alpha-pinene, beta-pinene, camphor, vitamin A betacarotene, and isopropenyl-1-methylcyclohexene.<br><br>
  11. 11. The method of claim 1 in which said substance consists of an unsaturated oil selected from the group consisting of oleic acid, linoleic acid, palmitoleic acid and vaccenic acid.<br><br>
  12. 12. The method of claim 1 in which said substance consists of sodium bicarbonate.<br><br>
  13. 13. The method of claim 1 in which said substance consists of potassium bicarbonate.<br><br>
  14. 14. The method of claim 1 in which said substance consists of monoammonium phosphate.<br><br>
  15. 15. The method of claim 1 in which said substance consists of alkali metal halides selected from the group consisting of sodium chloride, potassium chloride, sodium bromide and potassium bromide.<br><br>
  16. 16.<br><br>
    The method of claim 1 in which said substance consists of urea.<br><br>
    -13-<br><br>
    jo§$<br><br>
  17. 17. The method of claim 1 in which the hydrofluorocarbon is selected from the group consisting of trifLuouromethane (CF3H),<br><br>
    1,1,1,2,3,3 -hexafluoropropane (CF3CHFCF2H),<br><br>
    1,1,1,3,3,3-hexafluoropropane (CF3CH2CF3),<br><br>
    1,1,2,2,3,3-hexafluoropropane (HCF2CF2CF2H),<br><br>
    1,1,1,2,3,3,3-heptafluoropropane (CF3CHFCF3),<br><br>
    1,1,1,2,2,3,3-heptafluoropropane (CF3(CF2CF2H),<br><br>
    1,1,1,2,2,3,3,4,4-nonafluorobutane (CF3CF2CF2CF2H), 1,1,1,2,3,4,4,4-octafluorobutane (CF3CHFCHFCF3)<br><br>
    1,1,1,3,3,3-hexafluorobutane (CF3CH2CH2CF3),<br><br>
    C3H3FS, C4H3F7, C5HFu, CjH2F10,<br><br>
    C5H3F9, C5H4F8 and C5H5F7<br><br>
  18. 18. A method according to any one of claims 1 to 17, substantially as herein described.<br><br>
    By the authorised agents AJ PARK &amp; SON<br><br>
    </p>
    </div>
NZ283089A 1994-03-28 1995-03-21 Ozone-friendly fire extinguishing compositions containing hydrofluorocarbons and acid-scavenging additives and methods NZ283089A (en)

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JP (1) JPH09510891A (en)
KR (1) KR970702089A (en)
AU (1) AU2103995A (en)
CA (1) CA2185910A1 (en)
HU (1) HU9602662D0 (en)
IL (1) IL113086A0 (en)
MX (1) MX9604320A (en)
NO (1) NO964046D0 (en)
NZ (1) NZ283089A (en)
PL (1) PL316629A1 (en)
WO (1) WO1995026218A1 (en)
ZA (1) ZA952385B (en)

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ZA952385B (en) 1995-12-14
WO1995026218A1 (en) 1995-10-05
NO964046L (en) 1996-09-26
EP0752900A1 (en) 1997-01-15
IL113086A0 (en) 1995-06-29
NO964046D0 (en) 1996-09-26
KR970702089A (en) 1997-05-13
HU9602662D0 (en) 1996-11-28
AU2103995A (en) 1995-10-17
JPH09510891A (en) 1997-11-04
PL316629A1 (en) 1997-02-03
CA2185910A1 (en) 1995-10-05

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