WO1998032788A1 - Process for the production of synthetic resin foams - Google Patents
Process for the production of synthetic resin foams Download PDFInfo
- Publication number
- WO1998032788A1 WO1998032788A1 PCT/JP1998/000165 JP9800165W WO9832788A1 WO 1998032788 A1 WO1998032788 A1 WO 1998032788A1 JP 9800165 W JP9800165 W JP 9800165W WO 9832788 A1 WO9832788 A1 WO 9832788A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- foam
- mixture
- boiling point
- blowing agent
- 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.)
- Ceased
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/12—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent
- C08J9/14—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a physical blowing agent organic
- C08J9/149—Mixtures of blowing agents covered by more than one of the groups C08J9/141 - C08J9/143
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2203/00—Foams characterized by the expanding agent
- C08J2203/14—Saturated hydrocarbons, e.g. butane; Unspecified hydrocarbons
- C08J2203/142—Halogenated saturated hydrocarbons, e.g. H3C-CF3
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
Definitions
- the present invention relates to a method for producing a polyurethane or polyisocyanurate foam, and in particular, is characterized by the use of a specific low-boiling organic compound-based foaming agent.
- the present invention relates to a method for producing a synthetic resin foam.
- 1,1,1,1,3,3—Pentaforenoprono, 0 is a non-flammable compound with a boiling point of 15 ° C, and is a fluorine compound containing hydrogen atoms. Since it is a hydrocarbon, it is thought that there is little risk of depletion of the ozone layer and global warming, and its boiling point is close to CFC-11, making it nonflammable As a result, it is attracting attention as a very promising candidate as an alternative to CFC-11.
- HFC-2424fa has a slightly lower boiling point and, at high ambient temperatures, evaporates quickly, making foam production difficult and has low solubility in polyols.
- phase separation is apt to occur, and there is a problem that the range of usable polyols is limited.
- the present invention relates to a method for producing a synthetic resin foam having excellent heat insulating properties, mechanical strength, and the like, which has no risk of destruction of the ozone layer, has a small influence on global warming, and has a low flame retardancy.
- the main object of the present invention is to provide a method of using a foaming agent which has a proper boiling point with good compatibility and has good compatibility with the foam raw material.
- the present inventor has conducted studies in view of the above-mentioned problems in the prior art, and as a result, in the presence of a foaming agent, caused a reaction between a polyol and a polyisocyanate compound.
- 1,1,1,3,3—pentafluoropropane is used as a foaming agent.
- HFC—245 fa Use a mixture of 5 to 95% by weight and 95 to 5% by weight of hydrocarbon having a boiling point in the range of 20 to 70 ° C.
- the present invention comprises reacting a polyol with a polyisocyanate compound in the presence of a low-boiling organic compound-based foaming agent to produce a polyurethane or a polyisocyanate.
- the boiling point is 1,1,1,3,3-pentapentanoprono, 0 to 5 to 95% by weight as a low-boiling organic compound-based blowing agent.
- the present invention relates to a method for producing a synthetic resin foam characterized by using a mixture consisting of 95 to 5% by weight of hydrocarbons in the range of 20 to 70 ° C.
- the low-boiling organic compound-based blowing agent used in the present invention comprises 1,1,1,3,3-pentapentanoprono, 0 -one (HFC-2245fa) 5-95% by weight, It is a mixture consisting of 95 to 5% by weight of hydrocarbons having a boiling point in the range of 20 to 70 ° C.
- hydrocarbons having a boiling point in the range of 20-70 ° C include 2-methylbutane (boiling point 30 ° C) and n-penne (boiling point 35 ° C).
- 2, 2-dimethylbutane (boiling point 50 ° C), 2,3-dimethylinobutane (boiling point 58 ° C), cyclopentane (boiling point 50 ° C), 2-methyltilpe And the like (boiling point: 62 ° C), and cyclopentane is particularly preferred.
- These hydrocarbons can be used alone or in combination of two or more.
- hydrocarbons foam efficiently due to their lower molecular weight than HFC-245-fa, and their high boiling point prevents evaporation even at high ambient temperatures. This makes it easier to produce foam.
- hydrocarbons were thought to be poorly soluble in polyols by themselves, but synergistically with hydrocarbons by mixing with HFC-245 4a. It has been found that the solubility in the real can be improved-a wider range of polyols can be used.
- HFC-245fa which is a non-combustible component, is easily evaporated at a low boiling point, the evaporation of hydrocarbons, which is a flammable component, is suppressed. It was found that the use of a mixture of and could broaden the range of the mixture composition that would be flame-retardant.
- the mixing ratio of HFC_2 4 5fa and hydrocarbon is the former It can be arbitrarily selected from the range of 5 to 95% by weight, and the latter 95 to 5% by weight, depending on the application and formulation, but the boiling point of the mixture is 20 to 3%.
- a mixing ratio of about 0 ° C is particularly preferable.
- the mixing ratio of such a boiling point in the range of 20 to 30 ° C. is as follows for each of the above-mentioned hydrocarbons. However, since hydrocarbons are flammable, it is preferable that the proportion be as small as possible.
- blowing agents in the present invention are 1,1,1,3,3—pentafunoleprono.
- HFC — 2445 ⁇ a is a mixture of 50 to 95% by weight and cyclopentane 5 to 50% by weight.
- the low-boiling organic compound-based blowing agent comprising the specific mixture in the present invention can be used alone, or can be used in combination with another blowing agent or water.
- water is often used in combination with the low-boiling organic compound-based blowing agent.
- 1,1—Dicyclone can be used in combination with foaming agents other than water.
- Mouth 1 phenolic, methane, 1,1, 1, 2, 2 — low-boiling halogenated hydrocarbons such as tetrafluorobenzene, air, nitrogen, and carbon dioxide
- an inert gas such as o
- the proportion of the specific low-boiling organic compound-based blowing agent of the present invention in all the blowing agents is at least 20% by weight, particularly at least 40% by weight. I like it.
- the amount of the foaming agent used in the production of the synthetic resin foam is usually about 1 to 100 parts by weight, preferably about 100 to 100 parts by weight of the polyol. Or about 10 to 30 parts by weight.
- the foaming agent of the present invention may optionally contain a decomposition inhibitor.
- decomposition inhibitors include:-Nitrobenzene, Nitromethane and other two-troy compounds, a-methinorestylene, P-isoproveninole tonoleene Aromatic hydrocarbons such as isoprene, 2, 3 — aliphatic unsaturated hydrocarbons such as dimethyl butadiene, 1, 2 — butylene oxide, epichloro phenol Preferred are epoxide compounds such as phenolic compounds, p-t—butinolecate, 2, 6—di-t—butynolep-p—phenol compounds such as cresol, etc. Can be illustrated.
- the mixing ratio of these decomposition inhibitors is usually used in the present invention. It is preferable to use about 0.05 to 5 parts by weight per 100 parts by weight of the low-boiling organic compound-based blowing agent.
- the decomposition inhibitor may be dissolved in advance in the low-boiling organic compound-based blowing agent used in the present invention, or may be added separately at the time of foaming.
- known materials can be used as other raw materials used for producing the polyisocyanurate foam. The following can be exemplified as these.
- polyisocyanate compounds include those described in, for example, Keiji Iwata, Polyurethane Resin Handbook, pp. 71-98, Nikkan Kogyo Shimbun. Any of aliphatic, alicyclic, and aromatic organic isocyanates can be used.
- the most commonly used polyisolates are mainly 2,4 — trirange sociates (2, 4 — TDI), 2, 6 — There is a tri-isolate (2, 6—TDI), etc., and mainly a mixture of 2,4-TDI / 2,6—a weight ratio of 80 1 to 800 2. 5 Used as a mixture of Z35.
- polymethylene polyphenylene isocyanate (crude—MDI) obtained by phosgenating a condensate of aniline and formaldehyde is used. Has been done.
- Polyols include, for example, “Keiji Iwata, Poliure Polyether hand polyols and polyester terpolyols described in ⁇ Tanresin Handbook pp. 99-117, Nikkan Kogyo Shimbun '' etc. can be used. .
- polyether polyols can be obtained by the reaction of an alkylene oxide with an initiator having an active hydrogen atom.
- initiators such as ethylene glycol, trimethylolpropane, glycerin, trienonorenoamine, ethylenamine, and methyl alcohol , Trimethylamine, sonoreitol, sucrose, etc.
- alkylene oxide such as ethylene oxide and propylene oxide. Therefore, those having 2 to 8 functional groups and a hydroxyl value of 300 to 80 Omg KOH / g obtained by reacting both can be used.o
- Polyester polyols include condensed polyester polyols obtained by dehydration condensation of adipic acid with glycol or toluene, Among the lactone-based polyesters and polycarbonate diols obtained by ring-opening polymerization of the term, the number of functional groups is 2 to 4 and the hydroxyl value is 250 to 50. O mg KOH / g can be used.
- Catalysts include tertiary amines, organometallic compounds, etc. These mixtures can be used. Usually poly
- the catalyst is used in an amount of about 0.01 to 10 parts by weight, preferably about 0.1 to 5 parts by weight, based on 100 parts by weight.
- tertiary amines examples include monoamines such as tri-tinoleamine, dimethinorecyclohexinoleamine, and tetramethylethylene diamine.
- Diamines such as pentamethylethylhexamethylenediamine, triethylenediamine, 1,2—Dimethylimidazocyclic, etc.
- amines such as dimethinoleaminoethanol and the like.
- organometallic compound include starch zoate, dibutyltin dilaurate, dibutyltin diacetate, and lead octylate.
- foam stabilizers silicone-based and fluorine-containing surfactants are used as foam stabilizers.
- Po Li Shi Russia hexa emissions - Ru can that you use port re alkylene les Nburo click co Po Li-mer, etc.
- the main Chirupo Li Shi b hexa emissions surfactants you base Usually, the foam stabilizer can be used in an amount of about 0.1 to 10 parts by weight based on 100 parts by weight of the polyol.
- a polyolefin is used in the presence of the specific low-boiling organic compound-based blowing agent described above.
- Polyurethane or polyisocyanurate foam can be obtained by reacting the polyester with a polyisocyanate compound.
- the mixing ratio between the polyol and the polyisocyanate compound may be determined as appropriate.
- the isocyanate group in the polyisocyanate compound is used.
- the production conditions may be in accordance with a conventional method, and any production apparatus may be used as long as it can uniformly mix the raw materials.
- the production apparatus include a mixer and a foaming machine.
- the raw materials such as polyols, polyisocyanate compounds, foaming agents, catalysts, and other additives are mixed well and molded to form It can be the desired foam. Blowing agents and other additives are usually pre-dissolved in a polyol component and used as a premix, which makes it easier to obtain a uniform foam.
- the present invention is not limited to this, and it can be preliminarily dissolved in a polyisocyanate compound.
- the low-boiling organic compound-based blowing agent used in the present invention does not have a risk of destroying the ozone layer and has a small influence on global warming. It has excellent compatibility with raw materials, and in the presence of this blowing agent, By reacting the components, a synthetic resin foam having excellent heat insulating properties, mechanical strength, and the like can be obtained.
- polyol and the foaming agent used in the following examples are as follows.
- Polyolefin (ii) Polyether polyol with a hydroxyl value of 440, obtained by reacting propylene oxide with tridiamine.
- the mixed blowing agent used in the present invention showed good compatibility with the polyol in the mixing ratio actually used, and was stable. It was confirmed that a remix was formed.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Description
Claims
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU54972/98A AU5497298A (en) | 1997-01-28 | 1998-01-16 | Process for the production of synthetic resin foams |
| DE69825425T DE69825425T2 (de) | 1997-01-28 | 1998-01-16 | Verfahren zur Herstellung von Schäumen synthetischer Harze |
| EP98900412A EP0960902B1 (en) | 1997-01-28 | 1998-01-16 | Process for the production of synthetic resin foams |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1373597A JP3599079B2 (ja) | 1997-01-28 | 1997-01-28 | 合成樹脂発泡体の製造方法 |
| JP9/13735 | 1997-01-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1998032788A1 true WO1998032788A1 (en) | 1998-07-30 |
Family
ID=11841521
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP1998/000165 Ceased WO1998032788A1 (en) | 1997-01-28 | 1998-01-16 | Process for the production of synthetic resin foams |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP0960902B1 (ja) |
| JP (1) | JP3599079B2 (ja) |
| AU (1) | AU5497298A (ja) |
| DE (1) | DE69825425T2 (ja) |
| WO (1) | WO1998032788A1 (ja) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999036486A1 (en) * | 1998-01-16 | 1999-07-22 | E.I. Du Pont De Nemours And Company | 1,1,1,3,3-pentafluoropropane compositions |
| WO2001018099A1 (en) * | 1999-09-10 | 2001-03-15 | Alliedsignal Inc. | Use of 1,1,1,3,3-pentafluoropropane as a flame suppressant in c2-c6 hydrocarbon blown polyurethane foam |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0882760B1 (en) * | 1997-06-03 | 2003-11-05 | Asahi Glass Company Ltd. | Method for producing foamed synthetic resin |
| EP0927738A3 (en) * | 1997-12-30 | 2000-12-20 | Basf Corporation | Integral skin foams employing pentafluoropropane blowing agents |
| ATE371697T1 (de) | 2000-12-21 | 2007-09-15 | Dow Global Technologies Inc | Treibmittelzusammensetzungen, enthaltend teilfluorierte fluorkohlenwasserstoffe und einen niedrigsiedenden alkohol und/oder eine niedrigsiedende carbonylverbindung |
| ATE413428T1 (de) | 2000-12-21 | 2008-11-15 | Dow Global Technologies Inc | Treibmittelzusammensetzung und polymerschaum enthaltend ein normalerweise flüssiger hydrofluorkohlenwasserstoff und kohlenstoffdioxid |
| JP5105461B2 (ja) * | 2006-02-20 | 2012-12-26 | 東洋ゴム工業株式会社 | 研磨パッド |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239251A (ja) * | 1991-11-18 | 1993-09-17 | Daikin Ind Ltd | フルオロプロパンからなる発泡剤およびプラスチック発泡体の製造方法 |
| JPH09111032A (ja) * | 1995-09-26 | 1997-04-28 | Solvay & Cie | ポリウレタン又はポリイソシアヌレートフォームの調製のためのプレミックス |
| JPH09176059A (ja) * | 1995-12-22 | 1997-07-08 | Bayer Corp | 1,1,1,3,3−ペンタフルオロプロパン及び2−メチルブタンからなる共沸混合物様組成物 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19502578A1 (de) * | 1995-01-27 | 1996-08-01 | Bayer Ag | Neue Polyetherpolyole, Polyformulierung enthaltend diese Polyetherpolyole und deren Verwendnung zur Herstellung von harten Polyurethanschaumstoffen |
| US5672294A (en) * | 1996-04-10 | 1997-09-30 | Alliedsignal Inc. | Azeotrope-like compositions of 1,1,1,3,3-pentaflurorpropane and hydrocarbons |
-
1997
- 1997-01-28 JP JP1373597A patent/JP3599079B2/ja not_active Expired - Fee Related
-
1998
- 1998-01-16 DE DE69825425T patent/DE69825425T2/de not_active Expired - Fee Related
- 1998-01-16 WO PCT/JP1998/000165 patent/WO1998032788A1/ja not_active Ceased
- 1998-01-16 AU AU54972/98A patent/AU5497298A/en not_active Abandoned
- 1998-01-16 EP EP98900412A patent/EP0960902B1/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05239251A (ja) * | 1991-11-18 | 1993-09-17 | Daikin Ind Ltd | フルオロプロパンからなる発泡剤およびプラスチック発泡体の製造方法 |
| JPH09111032A (ja) * | 1995-09-26 | 1997-04-28 | Solvay & Cie | ポリウレタン又はポリイソシアヌレートフォームの調製のためのプレミックス |
| JPH09176059A (ja) * | 1995-12-22 | 1997-07-08 | Bayer Corp | 1,1,1,3,3−ペンタフルオロプロパン及び2−メチルブタンからなる共沸混合物様組成物 |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP0960902A4 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999036486A1 (en) * | 1998-01-16 | 1999-07-22 | E.I. Du Pont De Nemours And Company | 1,1,1,3,3-pentafluoropropane compositions |
| WO2001018099A1 (en) * | 1999-09-10 | 2001-03-15 | Alliedsignal Inc. | Use of 1,1,1,3,3-pentafluoropropane as a flame suppressant in c2-c6 hydrocarbon blown polyurethane foam |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0960902A4 (en) | 2001-11-21 |
| EP0960902A1 (en) | 1999-12-01 |
| DE69825425T2 (de) | 2005-08-11 |
| DE69825425D1 (de) | 2004-09-09 |
| JPH10204202A (ja) | 1998-08-04 |
| EP0960902B1 (en) | 2004-08-04 |
| AU5497298A (en) | 1998-08-18 |
| JP3599079B2 (ja) | 2004-12-08 |
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