WO2005047377A1 - Wärmeformbeständige polymethacrylimid-schaumstoffe mit feinen poren - Google Patents
Wärmeformbeständige polymethacrylimid-schaumstoffe mit feinen poren Download PDFInfo
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- WO2005047377A1 WO2005047377A1 PCT/EP2004/008218 EP2004008218W WO2005047377A1 WO 2005047377 A1 WO2005047377 A1 WO 2005047377A1 EP 2004008218 W EP2004008218 W EP 2004008218W WO 2005047377 A1 WO2005047377 A1 WO 2005047377A1
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- 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
- C08J9/141—Hydrocarbons
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
- B32B5/18—Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer of foamed material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1804—C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
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- 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
- C08J9/06—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 chemical blowing agent
- C08J9/10—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 chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
- C08J9/102—Azo-compounds
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/24—Homopolymers or copolymers of amides or imides
-
- 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
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/24—Homopolymers or copolymers of amides or imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
Definitions
- the invention relates to compositions for the production of heat-resistant polymethacrylimide foams with particularly fine pores, to processes for their preparation, processing and use of these foams.
- PMI foams Polymethacrylimide foams
- ROHACELL ® Polymethacrylimide foams
- these foams find many applications in particular in the field of coating materials (laminates, composites, foam composite bodies, sandwich constructions, sandwiches).
- Coating materials are shaped bodies which are composed of an outer covering layer and an inner core material.
- the cover layers used are materials that can absorb uniaxial or multiaxial extremely high tensile forces. Examples are glass and carbon fiber fabric or aluminum plates, which are fixed with adhesive resins on the core material.
- the core materials used are preferably materials with low densities, typically in the range of 30 kg / m 3 and 200 kg / m 3 .
- balsa wood There are three classes of core materials.
- the first class is balsa wood. Balsa wood can absorb high tensile and compressive forces due to its fiber structure, especially in the fiber direction, while it has only weak mechanical properties perpendicular thereto. Balsa wood is therefore a strongly anisotropic material. The average density is relatively high at -150 kg / m 3 , but is still sufficiently low for many applications.
- Such core materials are marketed under the brand name Baltec ® from the manufacturer DIAB.
- honeycomb structures such as Nomex ® honeycombs or aluminum honeycombs.
- Honeycomb structures are characterized by particularly low densities with high load capacity in the longitudinal direction of the honeycomb. In this regard, honeycombs are superior to other core materials.
- honeycombs are superior to other core materials.
- honeycombs if forces occur perpendicular to the honeycomb direction during processing or in the finished component, then honeycombs less suitable because they are mechanically weak perpendicular to the longitudinal direction by design.
- Another disadvantage is that the resin used to make the sandwich construction can run into the honeycomb, thus increasing the overall weight of the construction. This greatly limits the range of methods available for making honeycomb sandwich structures. In particular, the use of low-viscosity resin systems, as used for example in resin injection process, with honeycomb excluded. Another problem is the workability of the honeycomb, which is very complex and therefore expensive especially in less simple shaped bodies.
- the third class is closed-cell polymer foams. Isotropic foams are able to absorb shear forces in all spatial directions. Advantageous is the ease of machining, which can be done with the usual tools and wood in wood. In addition, certain rigid foams, such as, for example ROHACELL ®, thermoformed can. A significant advantage of closed-cell rigid foams is that no resin can penetrate, which would increase the total weight.
- resin infusion processes have been developed for making sandwiches.
- the sandwich core is covered by dry fiber material and soaked in a closed mold or in an airtight bag of low viscosity resin.
- the advantage of these methods lies, on the one hand, in a wider range of resin system and fiber materials and, on the other hand, in a better automatability. Sandwich constructions can therefore usually be produced cheaper with the aid of these methods.
- resin infusion techniques include Resin Transfer Molding (RTM), Resin Infusion Molding (RIM), Seeman's Resin Infusion Molding Process (SCRIMP), and Vacuum Assisted Resin Infusion (VARI).
- Table 1 Oil absorption of some polymer foams with densities in the range 60-80 kg / m 2 . Dense oil intake
- a square plate made of ROHACELL ® 71 RIST of dimensions 1000x1000x10mm 3 weighs 0.72 kg, but absorbs 0.46 kg of resin during processing.
- a corresponding plate made of ROHACELL ® 71 WF even absorbs 0.96 kg of resin, ie more than its own weight.
- DE2726260 describes the preparation of polymethacrylimide foams (PMI foams) which have excellent mechanical properties even at high temperatures.
- the production of the foams takes place in Casting process, ie monomers and required additives are mixed and polymerized in a chamber.
- the polymer is foamed by heating in a second step.
- a disadvantage of the foams described in DE2726260 is their coarse pore structure. By varying the blowing agents, the pore size can already be significantly reduced, but is still too coarse for the production of core materials for resin injection process (Comparative Example 1) and shows a nonuniform pore size distribution ( Figure 1).
- anti-settling agents such as, for example, Aerosil and carbon blacks or thickeners, such as soluble, high molecular weight polymers
- these anti-settling agents have to be added to the monomer mixture and these have to be worked into the mixtures in a complex manner together with the nucleating agent.
- Fine-pore foams based on PMI were also described in EP 532023 (Comparative Example 7).
- the method described there has various serious disadvantages. Relatively high concentrations of initiator were used for the polymerization, so that the resulting polymer has only a weight average molecular weight in the range of 50-500 kDa, despite the preparation in the casting process. Furthermore, the recipe no crosslinker was added. The resulting foams have for these reasons only a low heat resistance and a poor creep behavior.
- Fine-pore foams are known and are marketed under the name ROHACELL ® from Röhm GmbH & Co KG. It is possible one Fine porosity by a variation of blowing agents or by the addition of insoluble nucleating agents to achieve. However, the problem is that the fine porosity achieved via a variation of the blowing agent is not always sufficient. Finer-pore materials can be made by the use of insoluble nucleating agents, but the latter require the use of anti-settling agents, which entails increased expense in production.
- the object of the invention was therefore to find formulations for the production of particularly fine-pored PMI foams, without resorting to the use of insoluble nucleating agents.
- the foams should also have the same good thermo-mechanical properties as the known PMI foams.
- the object is achieved by a process for the preparation of foamable crosslinked polymers by adding a mixture of
- (D) 0.01-10 w / w crosslinkers i. (D1) free-radically polymerizable, polyunsaturated compounds and / or (D2) ionic crosslinking agent in the form of a salt, containing an at least divalent metal cation which is soluble in the monomer mixture,
- the invention also relates to a foamable crosslinked polymer
- (D) 0.01-10 w / w crosslinkers i. (D1) free-radically polymerizable, polyunsaturated compounds and / or (D2) ionic crosslinking agent in the form of a salt, containing an at least divalent metal cation which is soluble in the monomer mixture,
- (F) 0 to 20 wt% of conventional additives such as e.g. Antistatics, antioxidants, mold release agents, lubricants, dyes, flame retardants, flow improvers, fillers, light stabilizers and organic phosphorus compounds such as phosphites or phosphonates, pigments, release agents, weathering inhibitors and plasticizers.
- conventional additives such as e.g. Antistatics, antioxidants, mold release agents, lubricants, dyes, flame retardants, flow improvers, fillers, light stabilizers and organic phosphorus compounds such as phosphites or phosphonates, pigments, release agents, weathering inhibitors and plasticizers.
- foams with large molecular weights can be produced by the process according to the invention, which have excellent thermomechanical properties due to the low proportion of tert-butyl methacrylate or tert-butyl acrylate.
- Good foams are obtained using 0.01-15 wt% tert-butyl methacrylate and / or tert-butyl acrylate.
- Larger proportions of tert-butyl methacrylate or tert-butyl acrylate lead to softening of the polymer, which leads to a deterioration of the thermomechanical properties (Comparative Example 7a).
- foamable polymers having molecular weights> 600 kDa, which can be further processed into very fine-pored foams.
- foamable polymers 0.01-10 GewT, preferably 0.05-3 GewT Vernetzer must be added.
- 0.01-10 GewT preferably 2-8 GewT propellant must be added.
- Examples of the other vinylically unsaturated monomers mentioned under (A) are: acrylic or methacrylic acid and their esters with lower alcohols having 1-4 C atoms, styrene, maleic acid or its anhydride, itaconic acid or its anhydride, vinylpyrrolidone, vinyl chloride and / or vinylidene chloride.
- the proportion of comonomers which can not or only with great difficulty be cyclized to anhydride or imide should not exceed 30% by weight, preferably 20% by weight and more preferably 10% by weight, based on the weight of the monomers.
- blowing agent (C) formamide, formic acid, urea, itaconic acid, citric acid, dicyandiamide, water, monoalkylureas, dimethylurea, 5,5'-azobis-5-ethyl-1,3-dioxane , 2,2'-azo-bis-isobutyric acid butylamide, 2,2'-azo-bis-isobutyric acid N-diethylamide, 2,2 ', 4,4,4', 4'-hexamethyl-2,2'-azopentane, 2,2'-azo-bis-2-methyl-propane, dimethyl carbonate, di-tert-butycarbonate,
- Triethyl methane tricarboxylate and monohydric alcohols of 3-8 carbon atoms, e.g. Propanol-1, propanol-2, butanol-1, butanol-2, tert-butanol and iso-butanol.
- crosslinker D
- D1 covalent crosslinkers
- ie polymerizable polyunsaturated compounds As such monomers z.
- Another group which may be considered are ionic crosslinkers (D2).
- polyvalent metal cations that form ionic bridges between the acid groups of the copolymers.
- examples include the acrylates or methacrylates of alkaline earth metals or zinc. Zn and Mg (meth) acrylates are preferred.
- the (meth) acrylate salts can also be obtained by dissolving e.g. be prepared by ZnO or MgO in the monomer mixture.
- initiators compounds and initiator systems which can initiate radical polymerizations.
- Known classes of compounds are peroxides, hydroperoxides, peroxodisulfates, percarbonates, perketals, peroxyesters, hydrogen peroxide and azo compounds.
- Examples of initiators are hydrogen peroxide, dibenzoyl peroxide, dicyclohexyl peroxodicarbonate, dilauryl peroxide,
- Methyl ethyl ketone peroxide acetyl acetone peroxide, di-tert-butyl peroxide, tert-butyl hydroperoxide, cumene hydroperoxide, t-butyl peroctanoate, tert-butyl per-2-ethylhexanoate, tert-butyl perneodecanoate, tert-amyl perpivalate, tert-butyl perpivalate, tert-butyl perbenzoate, lithium, sodium, Potassium and ammonium peroxodisulfate, azoisobutyronitrile, 2,2-azobisiso-2,4-dimethylvaleronitrile, 2,2-azobisisobutyronitrile, 2,2'-azobis (2) amidinopropane) dihydrochloride, 2- (carbamoylazo) isobutyronitrile and 4,4'-azobis (cyanovaleric
- redox initiators H. Rauch-Puntigam, Th. Völker, acrylic and methacrylic compounds, Springer, Heidelberg, 1967 or Kirk-Othmer, Encyclopedia of Chemical Technology, Vol. 1, pp. 286 et seq., John Wiley & Sons, 1 New York, 1978. It may be beneficial to combine initiators and initiator systems having different disintegration properties with respect to time and temperature.
- the initiators (E) are preferably used in amounts of from 0.01 to 2 parts by weight, more preferably from 0.15 to 1.5% by weight, based on the total weight of the monomers.
- additives can be added to the mixtures.
- additives include, but are not limited to, antistatics, antioxidants, mold release agents, lubricants, dyes, flow improvers, fillers, light stabilizers, and organic phosphorus compounds such as phosphites or phosphonates, pigments, release agents, weathering inhibitors, and plasticizers.
- Other possible additives are flame retardants.
- halogen-containing flame retardants some of which contain antimony oxides, it is also possible to use phosphorus-containing compounds. Phosphorus compounds are preferred because of lower smoke toxicity in case of fire.
- Phosphorus compounds include, but are not limited to, phosphines, phosphine oxides, phosphonium compounds, phosphonates, phosphites, and / or phosphates. These compounds may be of organic and / or inorganic nature, such as, for example, phosphoric acid monoesters, phosphonic acid monoesters, phosphoric diesters, phosphonic diesters and phosphoric acid triesters, and also polyphosphates.
- the poly (meth) acrylimide foams produced according to the invention it is possible to produce coating materials.
- the poly (meth) acrylimide foams according to the invention have a broad field of application. They can be used in automobiles, rail vehicles, aircraft, watercraft, spacecraft, machine parts, antennas, X-ray tables, speakers and pipes.
- the method according to the invention offers the following advantages:
- For the polymerization homogeneous, low-viscosity mixtures are used which can be prepared and further processed in a technically simple manner.
- the foams have a particularly homogeneous pore structure (Figure 2)
- the procedure was as described in Comparative Example 8 with the difference that no nucleating agent was used.
- the resulting foam had a density of 77 kg / m 3 .
- Example 3 Pore size and resin uptake of selected samples
- Example Foam density Pore size Resin uptake kg / m 3 ⁇ m kg / m 2 2 69 35 ⁇ 0.040 a) 8 77 100-200 0.061 9 77 Not determined 0.287 a) not measurable
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Claims
Priority Applications (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04763413A EP1678244B1 (de) | 2003-10-30 | 2004-07-23 | Wärmeformbeständige polymethacrylimid-schaumstoffe mit feinen poren |
CA2544043A CA2544043C (en) | 2003-10-30 | 2004-07-23 | Thermostable microporous polymethacrylimide foams |
DE502004005979T DE502004005979D1 (de) | 2003-10-30 | 2004-07-23 | Wärmeformbeständige polymethacrylimid-schaumstoffe mit feinen poren |
US10/577,815 US8722751B2 (en) | 2003-10-30 | 2004-07-23 | Thermostable microporous polymethacrylimide foams |
JP2006537075A JP4996252B2 (ja) | 2003-10-30 | 2004-07-23 | 熱形状安定性微孔質ポリメタクリルイミドフォーム |
PL04763413T PL1678244T3 (pl) | 2003-10-30 | 2004-07-23 | Odporne na odkształcenie cieplne, polimetakryloimidowe tworzywa piankowe o drobnych porach |
DK04763413T DK1678244T3 (da) | 2003-10-30 | 2004-07-23 | Varmeformfaste polymethacrylimidskumplast med små porer |
SI200430654T SI1678244T1 (sl) | 2003-10-30 | 2004-07-23 | Toplotno stabilne mikroporozne polimetakrilimidnepene |
IL175244A IL175244A (en) | 2003-10-30 | 2006-04-27 | Thermostable microporous polymethacrylimide foams |
KR1020067010626A KR101076213B1 (ko) | 2003-10-30 | 2006-05-30 | 열에 안정한 미세다공성 폴리메타크릴이미드 발포체 |
HK07103233.4A HK1096111A1 (en) | 2003-10-30 | 2007-03-27 | Thermostable microporous polymethacrylimide foams |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10350971A DE10350971A1 (de) | 2003-10-30 | 2003-10-30 | Wärmeformbeständige Polymethacrylimid-Schaumstoffe mit feinen Poren |
DE10350971.2 | 2003-10-30 |
Publications (1)
Publication Number | Publication Date |
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WO2005047377A1 true WO2005047377A1 (de) | 2005-05-26 |
Family
ID=34529990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2004/008218 WO2005047377A1 (de) | 2003-10-30 | 2004-07-23 | Wärmeformbeständige polymethacrylimid-schaumstoffe mit feinen poren |
Country Status (15)
Country | Link |
---|---|
EP (1) | EP1678244B1 (de) |
JP (1) | JP4996252B2 (de) |
KR (1) | KR101076213B1 (de) |
CN (1) | CN100390223C (de) |
AT (1) | ATE384095T1 (de) |
CA (1) | CA2544043C (de) |
DE (2) | DE10350971A1 (de) |
DK (1) | DK1678244T3 (de) |
ES (1) | ES2299854T3 (de) |
HK (1) | HK1096111A1 (de) |
IL (1) | IL175244A (de) |
PL (1) | PL1678244T3 (de) |
PT (1) | PT1678244E (de) |
TW (1) | TWI343928B (de) |
WO (1) | WO2005047377A1 (de) |
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JP2008167448A (ja) * | 2006-12-30 | 2008-07-17 | Goodyear Tire & Rubber Co:The | 電子装置用のアンテナ構造とその製造方法 |
CN100420702C (zh) * | 2005-07-28 | 2008-09-24 | 西北工业大学 | 一种maa/an共聚物泡沫塑料及其制备方法 |
DE102012102689A1 (de) | 2012-03-26 | 2013-09-26 | Airex Ag | Strukturelement sowie Verfahren zu dessen Herstellung |
WO2014124774A1 (de) * | 2013-02-15 | 2014-08-21 | Evonik Industries Ag | Perlpolymerisat zur herstellung von pmi-schäumen |
US11833703B2 (en) | 2020-10-29 | 2023-12-05 | Evonik Operations Gmbh | Process for producing foam panels for the production of foam films |
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DE102010040286A1 (de) | 2010-08-31 | 2012-03-01 | Evonik Röhm Gmbh | PMI-Schäume mit verbesserten mechanischen Eigenschaften, insbesondere mit erhöhter Reißdehnung |
DE102010042752A1 (de) | 2010-10-21 | 2012-04-26 | Evonik Degussa Gmbh | Neuartige Bauweise für PKW / NFZ Leichtbaukammerfelgen umfassend Bauweise, Materialkonzept, Konstruktionsmerkmale und Herstellverfahren |
CN102051012B (zh) * | 2010-11-30 | 2012-02-08 | 湖南兆恒材料科技有限公司 | 一种晶须改性聚甲基丙烯酰亚胺泡沫塑料及其制备方法 |
CN102225983B (zh) * | 2011-05-03 | 2013-04-24 | 浙江理工大学 | 一种含有酰亚胺基的聚合物泡沫材料及其制备方法 |
CN102432971A (zh) * | 2011-09-14 | 2012-05-02 | 刘天义 | 甲基丙烯亚胺泡沫塑料及其制备方法 |
DE102011085026A1 (de) | 2011-10-21 | 2013-04-25 | Evonik Röhm Gmbh | Verfahren zur Herstellung von Korngrenzenhaftung von expandierten Copolymeren auf Basis von Methacryl- und Acrylverbindungen und Anhaftung diverser Deckschichten auf dem Schaumkern |
DE102012208428A1 (de) | 2012-05-21 | 2013-11-21 | Evonik Industries Ag | Pul-Core-Verfahren mit PMI-Schaumkern |
EP2877342B1 (de) | 2012-07-24 | 2016-12-21 | Evonik Röhm GmbH | Neuer formgebungsprozess für pmi-schaumwerkstoffe bzw. daraus hergestellte compositebauteile |
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- 2004-07-23 EP EP04763413A patent/EP1678244B1/de active Active
- 2004-07-23 CN CNB2004800272104A patent/CN100390223C/zh active Active
- 2004-07-23 DK DK04763413T patent/DK1678244T3/da active
- 2004-07-23 ES ES04763413T patent/ES2299854T3/es active Active
- 2004-07-23 CA CA2544043A patent/CA2544043C/en not_active Expired - Fee Related
- 2004-07-23 JP JP2006537075A patent/JP4996252B2/ja active Active
- 2004-07-23 WO PCT/EP2004/008218 patent/WO2005047377A1/de active IP Right Grant
- 2004-07-23 PL PL04763413T patent/PL1678244T3/pl unknown
- 2004-07-23 DE DE502004005979T patent/DE502004005979D1/de active Active
- 2004-07-23 AT AT04763413T patent/ATE384095T1/de not_active IP Right Cessation
- 2004-08-10 TW TW093123939A patent/TWI343928B/zh not_active IP Right Cessation
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- 2006-04-27 IL IL175244A patent/IL175244A/en active IP Right Grant
- 2006-05-30 KR KR1020067010626A patent/KR101076213B1/ko active IP Right Grant
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Cited By (7)
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CN100420702C (zh) * | 2005-07-28 | 2008-09-24 | 西北工业大学 | 一种maa/an共聚物泡沫塑料及其制备方法 |
JP2008167448A (ja) * | 2006-12-30 | 2008-07-17 | Goodyear Tire & Rubber Co:The | 電子装置用のアンテナ構造とその製造方法 |
DE102012102689A1 (de) | 2012-03-26 | 2013-09-26 | Airex Ag | Strukturelement sowie Verfahren zu dessen Herstellung |
WO2013144130A1 (de) | 2012-03-26 | 2013-10-03 | Airex Ag | Strukturelement sowie verfahren zu dessen herstellung |
US9533468B2 (en) | 2012-03-26 | 2017-01-03 | Airex Ag | Structural element and method for the production thereof |
WO2014124774A1 (de) * | 2013-02-15 | 2014-08-21 | Evonik Industries Ag | Perlpolymerisat zur herstellung von pmi-schäumen |
US11833703B2 (en) | 2020-10-29 | 2023-12-05 | Evonik Operations Gmbh | Process for producing foam panels for the production of foam films |
Also Published As
Publication number | Publication date |
---|---|
JP2007513213A (ja) | 2007-05-24 |
DK1678244T3 (da) | 2008-05-13 |
CA2544043C (en) | 2012-05-15 |
KR20060130574A (ko) | 2006-12-19 |
JP4996252B2 (ja) | 2012-08-08 |
DE10350971A1 (de) | 2005-06-02 |
TWI343928B (en) | 2011-06-21 |
IL175244A (en) | 2011-01-31 |
EP1678244A1 (de) | 2006-07-12 |
PL1678244T3 (pl) | 2008-06-30 |
PT1678244E (pt) | 2008-04-22 |
CN100390223C (zh) | 2008-05-28 |
TW200514813A (en) | 2005-05-01 |
CN1856531A (zh) | 2006-11-01 |
EP1678244B1 (de) | 2008-01-16 |
ATE384095T1 (de) | 2008-02-15 |
CA2544043A1 (en) | 2005-05-26 |
KR101076213B1 (ko) | 2011-10-25 |
ES2299854T3 (es) | 2008-06-01 |
DE502004005979D1 (de) | 2008-03-06 |
HK1096111A1 (en) | 2007-05-25 |
IL175244A0 (en) | 2006-09-05 |
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