EP2083975A1 - Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques - Google Patents
Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniquesInfo
- Publication number
- EP2083975A1 EP2083975A1 EP07821531A EP07821531A EP2083975A1 EP 2083975 A1 EP2083975 A1 EP 2083975A1 EP 07821531 A EP07821531 A EP 07821531A EP 07821531 A EP07821531 A EP 07821531A EP 2083975 A1 EP2083975 A1 EP 2083975A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- wood
- range
- component
- light wood
- light
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 117
- 241000771208 Buchanania arborescens Species 0.000 title claims description 54
- 239000002023 wood Substances 0.000 claims abstract description 103
- 239000002245 particle Substances 0.000 claims abstract description 71
- 229920003023 plastic Polymers 0.000 claims abstract description 34
- 239000004033 plastic Substances 0.000 claims abstract description 34
- 239000011230 binding agent Substances 0.000 claims abstract description 31
- 239000000945 filler Substances 0.000 claims abstract description 25
- 239000000654 additive Substances 0.000 claims abstract description 14
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 72
- 229920003180 amino resin Polymers 0.000 claims description 35
- 229920005989 resin Polymers 0.000 claims description 35
- 239000011347 resin Substances 0.000 claims description 35
- 229920001577 copolymer Polymers 0.000 claims description 33
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 26
- 239000000126 substance Substances 0.000 claims description 21
- 238000004519 manufacturing process Methods 0.000 claims description 15
- 229920000877 Melamine resin Polymers 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 claims description 13
- 239000012948 isocyanate Substances 0.000 claims description 6
- 150000002513 isocyanates Chemical class 0.000 claims description 6
- 239000005022 packaging material Substances 0.000 claims description 6
- 238000010276 construction Methods 0.000 claims description 4
- HANVTCGOAROXMV-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine;urea Chemical compound O=C.NC(N)=O.NC1=NC(N)=NC(N)=N1 HANVTCGOAROXMV-UHFFFAOYSA-N 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 238000000465 moulding Methods 0.000 claims description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 2
- 229920001568 phenolic resin Polymers 0.000 claims description 2
- 239000005011 phenolic resin Substances 0.000 claims description 2
- 229920002647 polyamide Polymers 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920000582 polyisocyanurate Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims 1
- 239000010410 layer Substances 0.000 abstract description 35
- 238000003825 pressing Methods 0.000 abstract description 6
- 238000005187 foaming Methods 0.000 abstract description 4
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000002344 surface layer Substances 0.000 abstract 1
- 239000004793 Polystyrene Substances 0.000 description 27
- 229920002223 polystyrene Polymers 0.000 description 27
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 21
- 229920000642 polymer Polymers 0.000 description 19
- 239000003292 glue Substances 0.000 description 11
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 10
- -1 polyethylene Polymers 0.000 description 9
- 239000007787 solid Substances 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000010097 foam moulding Methods 0.000 description 8
- 239000011093 chipboard Substances 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 150000001299 aldehydes Chemical class 0.000 description 6
- 239000002216 antistatic agent Substances 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 239000011324 bead Substances 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- 239000007900 aqueous suspension Substances 0.000 description 4
- 238000005452 bending Methods 0.000 description 4
- 238000006068 polycondensation reaction Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 229920001169 thermoplastic Polymers 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- 241000218657 Picea Species 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000007688 edging Methods 0.000 description 3
- 229920006248 expandable polystyrene Polymers 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920006327 polystyrene foam Polymers 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241001070947 Fagus Species 0.000 description 2
- 235000010099 Fagus sylvatica Nutrition 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 description 2
- 229920005830 Polyurethane Foam Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229920002522 Wood fibre Polymers 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 2
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000004794 expanded polystyrene Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229910002804 graphite Inorganic materials 0.000 description 2
- 239000010439 graphite Substances 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 239000012778 molding material Substances 0.000 description 2
- CRSOQBOWXPBRES-UHFFFAOYSA-N neopentane Chemical compound CC(C)(C)C CRSOQBOWXPBRES-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000002984 plastic foam Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 2
- 229920001955 polyphenylene ether Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005629 polypropylene homopolymer Polymers 0.000 description 2
- 239000011496 polyurethane foam Substances 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- 239000002025 wood fiber Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical class C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 241001070941 Castanea Species 0.000 description 1
- 235000014036 Castanea Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 101100377706 Escherichia phage T5 A2.2 gene Proteins 0.000 description 1
- 241000218652 Larix Species 0.000 description 1
- 235000005590 Larix decidua Nutrition 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000219000 Populus Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920001131 Pulp (paper) Polymers 0.000 description 1
- 229920006328 Styrofoam Polymers 0.000 description 1
- 240000007313 Tilia cordata Species 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000006085 branching agent Substances 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- BZDKYAZTCWRUDZ-UHFFFAOYSA-N buta-1,3-diene;methyl 2-methylprop-2-enoate;prop-2-enenitrile;styrene Chemical compound C=CC=C.C=CC#N.COC(=O)C(C)=C.C=CC1=CC=CC=C1 BZDKYAZTCWRUDZ-UHFFFAOYSA-N 0.000 description 1
- NOQOJJUSNAWKBQ-UHFFFAOYSA-N buta-1,3-diene;methyl prop-2-enoate;styrene Chemical compound C=CC=C.COC(=O)C=C.C=CC1=CC=CC=C1 NOQOJJUSNAWKBQ-UHFFFAOYSA-N 0.000 description 1
- 150000003857 carboxamides Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 229920001870 copolymer plastic Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 238000009408 flooring Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229920012128 methyl methacrylate acrylonitrile butadiene styrene Polymers 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000001172 regenerating effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000009416 shuttering Methods 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000011145 styrene acrylonitrile resin Substances 0.000 description 1
- 229920001909 styrene-acrylic polymer Polymers 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000008261 styrofoam Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 230000005641 tunneling Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27N—MANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
- B27N3/00—Manufacture of substantially flat articles, e.g. boards, from particles or fibres
- B27N3/005—Manufacture of substantially flat articles, e.g. boards, from particles or fibres and foam
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
- Y10T428/249971—Preformed hollow element-containing
- Y10T428/249972—Resin or rubber element
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/253—Cellulosic [e.g., wood, paper, cork, rayon, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
- Y10T428/254—Polymeric or resinous material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2982—Particulate matter [e.g., sphere, flake, etc.]
- Y10T428/2991—Coated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31895—Paper or wood
- Y10T428/31899—Addition polymer of hydrocarbon[s] only
- Y10T428/31902—Monoethylenically unsaturated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31975—Of cellulosic next to another carbohydrate
- Y10T428/31978—Cellulosic next to another cellulosic
- Y10T428/31982—Wood or paper
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31989—Of wood
Definitions
- the present invention relates to a light wood-containing material having an average density in the range from 200 to 600 kg / m 3 , containing, in each case based on the wood-containing substance:
- 150 kg / m 3 selected from the group consisting of foamable plastic particles and already foamed plastic particles;
- component B) contains plasticized particles obtained by comminution of shaped bodies in an amount, based on component B), in the range from 1% by weight to 100% by weight.
- the present invention relates to a multilayer wood material containing the wood-containing material according to the invention, a process for the preparation of light wood-containing materials, a process for producing a multilayer wood material, the use of light wood-containing material according to the invention and the multilayer wood material according to the invention.
- Wood-based materials in particular multilayer wood-based materials, are a cost-effective and resource-saving alternative to solid wood and have gained great importance in particular in furniture construction, in laminate flooring and as building materials.
- As starting materials serve wood particles of different strengths, eg. As wood chips or wood fibers from different woods. Such wood particles are usually pressed with natural and / or synthetic binders and optionally with the addition of further additives to plate or strand-shaped wood materials.
- Lightweight wood-based materials result in easier handling of the products by the end customer, for example when packing, transporting, unpacking or constructing the furniture.
- Light wood-based materials lead to lower transport and packaging costs, and material costs can be saved in the production of lightweight wood-based materials.
- Light wood-based panels can, for example, when used in means of transport lead to lower energy consumption of these means of transport. Further, using lightweight wood-based materials, for example, costly decorative parts such as thicker worktops and kitchen cheeks that are currently in vogue can be offered more cheaply.
- tube chipboard and honeycomb panels are mentioned. Due to their special properties, tube chipboards are mainly used in the manufacture of doors as an inner layer.
- honeycomb panel for example, the too low screw extraction resistance, the difficulty attaching fittings and the difficulties in edging.
- binders are all customary binders suitable for the gluing of wood. desch, such as urea-formaldehyde resins, useful.
- Suitable fillers are foamable or already foamed plastic particles, preferably expandable thermoplastics such as styrene polymers.
- the plates described in the examples have a thickness of 18 to 21 mm, a density of 220 kg / m 3 to 430 kg / m 3 and an average bending strength of 3.6 N / mm 2 to 17.7 N / mm 2 on. Cross tensile strengths are not specified. CH 370229 does not comment on foamed plastic particles obtained by comminution of shaped bodies.
- WO 02/38676 describes a process for the preparation of light products, in which 5 to 40 wt .-% foamable or already foamed polystyrene having a particle size of less than 1 mm, 60 to 95 wt .-% lignocellulose-containing material and binder mixed and at elevated Temperature and elevated pressure are pressed to the finished product. The usual binders are mentioned.
- WO 02/38676 does not comment on foamed plastic particles obtained by comminution of shaped bodies.
- JP 06031708 describes light wood materials, wherein for the middle layer of a three-layer chipboard, a mixture of 100 parts by weight of wood particles and 5 to 30 parts by weight of particles of synthetic resin foam are used, said resin particles having a specific gravity of not more than 0.3 g / cm 3 and have a compressive strength of at least 30 kg / cm 2 . Further, it is described that the specific gravity of the wood particles should not exceed 0.5 g / cm 3 .
- the binders are not subject to restrictions according to JP 06031708. JP 06031708 does not comment on foamed plastic particles obtained by comminution of shaped bodies.
- Too low mechanical strength for example, lead to breaking or cracking of the components. Furthermore, these components tend during drilling or sawing to additional flaking of further wood material. Fastening hardware is difficult with these materials.
- the object of the present invention was to show light wood-containing materials and light wood materials, which in comparison to the commercial Wood materials have lower density with good mechanical strength and good processing properties.
- the mechanical strength can be determined, for example, by measuring the transverse tensile strength according to DIN EN 319 or the flexural strength according to DIN EN 310.
- these lightweight wood-based materials should preferably be producible using domestic European woods.
- the swelling value of the light wood materials should not be adversely affected by the reduced density.
- the object was achieved by a light wood-containing material having an average density in the range of 200 to 600 kg / m 3 , containing, in each case based on the woody substance:
- component B) contains foamy plastic particles obtained by comminution of shaped bodies in an amount, based on component B), in the range from 1% by weight to 100% by weight.
- the sum of components A) to D) is 100% by weight and is based on the solids of the wood-containing substance.
- the wood-containing substance may contain the usual small amounts of water (in a usual small range of variation); This water is not included in the weight of the present application.
- the weight of the wood particles refers to, in the usual manner known to those skilled, dried wood particles.
- the weight specification of the binder C) relates with respect to the aminoplast component in the binder to the solids content of the corresponding component (determined by evaporation of the water at 120 ° C., within 2 hours, for example, Günter Zeppenfeld, Dirk Grunwald, Klebstoffe in Wood and furniture industry, 2nd edition, DRW-Verlag, page 268).
- the weight of the binder C) refers to this Sustanz in terms of organic isocyanate having at least two isocyanate groups per se, ie without consideration of, for example, solvent.
- the light wood-containing substances according to the invention have an average density of 200 to 600 kg / m 3 , preferably 200 to 575 kg / m 3 , particularly preferably 250 to 550 kg / m 3 , in particular 300 to 500 kg / m 3 .
- the transverse tensile strength of the light wood-containing substances according to the invention or preferably of the multilayer wood-base materials according to the invention is in the range from 0.1 N / mm 2 to 1.0 N / mm 2 , preferably 0.3 to 0.8 N / mm 2 preferably 0.30 to 0.6 N / mm 2 .
- the flexural strength of the light wood-containing materials according to the invention or preferably of the multilayer wood-base materials according to the invention is in the range of 3 N / mm 2 to 30 N / mm 2 , preferably 5 to 25 N / mm 2 , particularly preferably 9 to 20 N / mm 2 .
- the determination of the bending strength is according to DIN EN 310.
- multilayer wood materials are all materials into consideration, which are made of wood veneer, preferably with an average density of the wood veneer from 0.4 to 0.85 g / cm 3 , for example, veneer or plywood boards or Laminated Veneer Lumber (LVL).
- wood veneer preferably with an average density of the wood veneer from 0.4 to 0.85 g / cm 3 , for example, veneer or plywood boards or Laminated Veneer Lumber (LVL).
- VLL Laminated Veneer Lumber
- multilayer wood materials are particularly all materials into consideration, which are made of wood chips, preferably with a mean density of wood chips from 0.4 to 0.85 g / cm 3 , for example chipboard or OSB boards, and wood fiber materials such as LDF, MDF and HDF plates. Particleboard and fiberboard, in particular chipboard, are preferred.
- the average density of the wood particles of component A) is generally 0.4 to 0.85 g / cm 3 , preferably 0.4 to 0.75 g / cm 3 , in particular 0.4 to 0.6 g / cm 3 .
- any wood species comes into question; For example, spruce, beech, pine, larch, linden, poplar, ash, chestnut or fir wood are very suitable; spruce and / or beech wood, in particular spruce wood, are preferred.
- the dimensions of the wood particles are not critical according to the current state of knowledge and, as usual, are based on the wood material to be produced, for example the wood-based materials mentioned above, such as chipboard or OSB.
- filler B are foamable yet compact or already foamed plastic particles, preferably thermoplastic plastic particles in question. But it can also be used plastic particles that are in any intermediate stage of foaming.
- Filler B contains plastic foam particles which can be obtained from molded articles, for example from polyurethane foam moldings, polyethylene foam moldings, polypropylene foam moldings or preferably polystyrene foam moldings, by comminution, preferably milling, in an amount in the range from 1% by weight to 100% by weight. -%, preferably in the range of 15 wt .-% to 85 wt .-%, particularly preferably in the range of 25 wt .-% to 75 wt .-%, most preferably in the range of 40 wt .-% to 60 wt .-%, in each case based on component B).
- plastic foam particles which can be obtained from molded articles, for example from polyurethane foam moldings, polyethylene foam moldings, polypropylene foam moldings or preferably polystyrene foam moldings, by comminution, preferably milling, in an amount in the range from 1% by weight to 100% by weight. -%, preferably in the range
- plastic particles according to the invention are referred to below as plastic particles according to the invention.
- foamed plastic or especially foam is explained, for example, in DIN 7726: 1982-05.
- Suitable polymers on which the plastic particles according to the invention are based are all polymers, preferably thermoplastic polymers, which can be foamed. These are known to the person skilled in the art.
- Highly suitable such polymers are, for example, PVC (hard and soft), polycarbonates, polyisocyanurates, polycarbodiimides, polyacrylimides and polymethacrylimides, polyamides, polyurethanes, aminoplast resins and phenolic resins, styrene homopolymers, styrene copolymers, C 2 -C 10 -olefin homopolymers, C 2 -C 10 -olefin copolymers and polyesters ,
- the 1-alkenes for example ethylene, propylene, 1-butene, 1-hexene, 1-octene.
- the plastic particles of component B) according to the invention have a bulk density of from 10 to 150 kg / m 3 , preferably from 15 to 80 kg / m 3 , particularly preferably from 20 to 70 kg / m 3 , in particular from 30 to 60 kg / m 3 .
- the bulk density is usually determined by weighing a volume filled with the bulk material.
- Foamed plastic particles according to the invention are generally used in the form of spheres or beads having an average diameter of advantageously 0.25 to 10 mm, preferably 0.5 to 5 mm, in particular 0.75 to 3 mm.
- Prefabricated plastic particle beads according to the invention advantageously have a small surface area per volume, for example in the form of a spherical or elliptical particle.
- the prefoamed plastic particle beads according to the invention are advantageously closed-celled.
- the open cell density according to DIN-ISO 4590 is usually less than 30%.
- Plastic foam particles which can be obtained from shaped articles, for example from polyurethane foam moldings, polyethylene foam moldings, polypropylene foam moldings or preferably polystyrene foam moldings, by comminution, preferably grinding, are generally irregular in shape but can also be spherical.
- the filler B consists of different types of polymers, ie types of polymers which are based on different monomers (for example polystyrene and polyethylene or polystyrene and homo-polypropylene or polyethylene and homo-polypropylene), these can be present in different weight ratios, which, however, according to current standards State of knowledge, not critical.
- thermoplastics of the invention additives, nucleating agents, plasticizers, flame retardants, soluble and insoluble inorganic and / or organic dyes and pigments, for.
- IR absorbers such as carbon black, graphite or aluminum powder, are added together or spatially separated as additives.
- Polystyrene and / or styrene copolymer in each case including those which are obtained by comminution of shaped bodies, are preferably used as the sole inventive plastic particle component in filler B).
- the filler polystyrene and / or styrene copolymer can be prepared by all polymerization processes known to those skilled in the art [see, for example, US Pat. Ullmann's Encyclopedia, Sixth Edition, 2000 Electronic Release]. For example, the preparation is carried out in a conventional manner by suspension polymerization or by extrusion.
- styrene In the suspension polymerization, styrene, optionally with the addition of further comonomers in aqueous suspension, is polymerized in the presence of a customary suspension stabilizer by means of free-radical-forming catalysts.
- the propellant and optionally further additives may be included in the polymerization be added to the batch in the course of the polymerization or after completion of the polymerization.
- the resulting peribular expandable styrene polymers are separated from the aqueous phase after the end of the polymerization, washed, dried and sieved.
- the blowing agent is mixed for example via an extruder in the polymer, conveyed through a nozzle plate and granulated into particles or strands.
- blowing agents are all blowing agents known to those skilled in the art, for example C3 to C6 hydrocarbons, such as propane, n-butane, isobutane, n-pentane, isopentane, neopentane and / or hexane, alcohols, ketones, ethers or halogenated hydrocarbons , Preferably, a commercially available Pentanisome- ren mixture is used.
- styrene polymers additives, nucleating agents, plasticizers, flame retardants, soluble and insoluble inorganic and / or organic dyes and pigments, for.
- IR absorbers such as carbon black, graphite or aluminum powder, are added together or spatially separated as additives.
- styrene copolymers these styrene copolymers advantageously have at least 50% by weight, preferably at least 80% by weight, of copolymerized styrene.
- comonomers come z.
- ⁇ -methyl styrene, ring-halogenated styrenes, acrylonitrile, esters of acrylic or methacrylic acid of alcohols having 1 to 8 carbon atoms, N-vinylcarbazole, maleic acid (anhydride), (meth) acrylamides and / or vinyl acetate into consideration.
- the polystyrene and / or styrene copolymer in copolymerized form contain a small amount of a chain splitter, d. H. a compound having more than one, preferably two, double bonds, such as divinylbenzene, butadiene and / or butanediol diacrylate.
- the branching agent is generally used in amounts of from 0.005 to 0.05 mole percent, based on styrene.
- styrene (co) polymers having molecular weights and molecular weight distributions as described in EP-B 106 129 and in DE-A 39 21 148. Preference is given to using styrene (co) polymers having a molecular weight in the range from 190,000 to 400,000 g / mol.
- Mixtures of different styrene (co) polymers can also be used.
- styrene to polymeric glassy polystyrene (GPPS), toughened polystyrene (HIPS), anionically polymerized polystyrene or toughened polystyrene (A-IPS), styrene- ⁇ -methylstyrene copolymers, acrylonitrile-butadiene-styrene polymers (ABS), styrene Acrylonitrile (SAN), acrylonitrile-styrene-acrylic ester (ASA), methyl acrylate-butadiene-styrene (MBS), methyl methacrylate-acrylonitrile-butadiene-styrene (MABS) polymers or mixtures thereof or used with polyphenylene ether (PPE).
- GPPS polymeric glassy polystyrene
- HIPS toughened polystyrene
- A-IPS anionically polymerized polystyrene or toughened polystyrene
- polystyrene Neopor ® and / or Peripor ® from BASF Aktiengesellschaft is particularly preferred ® Styrofoam used.
- Pre-expanded polystyrene and / or styrene copolymers are advantageously used.
- the prefoamed polystyrene can be prepared by all methods known to the person skilled in the art (for example DE 845 264).
- the expandable styrene polymers are expanded in a known manner by heating to temperatures above their softening point, for example with hot air or preferably steam.
- the prefoamed polystyrene or prefoamed styrene copolymer of component B) and the plastic particles of component B according to the invention obtained by comminution of corresponding polystyrene or styrene copolymer shaped articles advantageously have a bulk density of 10 to 150 kg / m 3 , preferably 15 to 80 kg / m 3 , more preferably 20 to 70 kg / m 3 , in particular 30 to 60 kg / m 3 .
- the prefoamed polystyrene or prefoamed styrene copolymer is advantageously used in the form of spheres or beads having an average diameter of advantageously 0.25 to 10 mm, preferably 0.5 to 5 mm, in particular 0.75 to 3 mm.
- the prefoamed polystyrene or prefoamed styrene copolymer spheres advantageously have a small surface area per volume, for example in the form of a spherical or elliptical particle.
- the prefoamed polystyrene or prefoamed styrene copolymer spheres are advantageously closed-cell.
- the open cell density according to DIN-ISO 4590 is usually less than 30%.
- foamed polystyrene or foamed styrene copolymer moldings of foamed styrene polymer or styrene copolymer can serve. These can be comminuted with the customary comminution methods to the degree of the individual styrene polymer or styrene copolymer particles, preferably spherical. A well suited and preferred shredding method is milling. Moldings of foamed styrene polymer or styrene copolymer can be prepared by the known methods and serve, for example, as packaging material or insulating material.
- foamed polystyrene or foamed styrene copolymer molded parts of foamed styrene polymer or styrene copolymer can be used, which are intended for disposal, for example, styrene polymer or Styrolcopolymerisatverpackungsmaterial waste or styrene polymer or styrene polymer insulation loss.
- the polystyrene or styrene copolymer or the prefoamed polystyrene or prefoamed styrene copolymer particularly preferably has an antistatic coating.
- antistatic agents the usual and common in the art substances can be used. Examples are N, N-bis (2-hydroxyethyl) -Ci 2 -C 18 -alkylamines, fatty acid diethanolamides, choline ester chlorides of fatty acids, C 12 -C 20 -alkyl sulfonates, ammonium salts.
- Suitable ammonium salts contain, in addition to alkyl groups, 1 to 3 hydroxyl-containing organic radicals on the nitrogen.
- Suitable quaternary ammonium salts are, for example, those which have 1 to 3, preferably 2, identical or different alkyl radicals on the nitrogen cation of 1 to 12, preferably 1 to 10, carbon atoms, and 1 to 3, preferably 2, identical or different hydroxyalkyl radicals. or hydroxyalkylpolyoxyalkylene radicals bonded, with any anion, such as chloride, bromide, acetate, methyl sulfate or p-toluenesulfonate.
- hydroxyalkyl and hydroxyalkyl-polyoxyalkylene radicals are those which are formed by oxyalkylation of a nitrogen-bonded hydrogen atom and are derived from 1 to 10 oxyalkylene radicals, in particular oxyethylene and oxypropylene radicals.
- An antistatic agent which is particularly preferred is a quaternary ammonium salt or an alkali metal salt, especially sodium salt of a C 12 -C 20 alkanesulfonate, eg. B emulsifier K30 from Bayer AG, or mixtures thereof.
- the antistatic agents can generally be added both as a pure substance and in the form of an aqueous solution.
- the antistatic agent can be added in the process for the preparation of polystyrene or styrene copolymer analogously to the customary additives or can be applied after the preparation of the polystyrene particles as a coating.
- the antistatic agent is advantageously used in an amount of 0.05 to 6 wt .-%, preferably 0.1 to 4 wt .-%, based on the polystyrene or styrene copolymer.
- the filler particles B) are advantageous even after pressing to light wood material, preferably multi-layer wood material, in a state in which their original shape is still recognizable.
- the total amount of filler B), based on the light wood-containing material, is in the range of 1 to 25 wt .-%, preferably 2 to 15 wt .-%, particularly preferably 3 to 12 wt .-%.
- the total amount of filler B) with polystyrene and / or styrene copolymer, in each case including one obtained by comminuting shaped bodies, as a single plastic particle component, based on the light wood-containing substance, is in the range from 1 to 25% by weight. %, preferably 2 to 15 wt .-%, particularly preferably 3 to 12 wt .-%.
- binder C it is possible to use all binders known to the person skilled in the art for the production of wood-based materials, for example aminoplast resins and / or organic isocyanates, such as PMDI.
- the binder C) generally contains the substances generally known to the person skilled in the art for aminoplast resins and usually referred to as hardeners, such as ammonium sulfate or ammonium nitrate or inorganic or organic acids, for example sulfuric acid, formic acid or acid regenerating substances, such as aluminum chloride, aluminum sulfate , in each case in the usual, small amounts, for example in the range of 0.1 wt .-% to 3 wt .-%, based on the total amount of aminoplast resin in the binder C).
- hardeners such as ammonium sulfate or ammonium nitrate or inorganic or organic acids, for example sulfuric acid, formic acid or acid regenerating substances, such as aluminum chloride, aluminum sulfate , in each case in the usual, small amounts, for example in the range of 0.1 wt .-% to 3 wt .-%, based on the total amount of aminoplast resin in the binder C).
- aminoplast resin are here polycondensation products of compounds having at least one, optionally partially substituted with organic radicals, carbamide group (the carbamide group is also called carboxamide) and an aldehyde, preferably formaldehyde understood.
- aminoplast resin As a suitable aminoplast resin, all of the specialist, preferably known for the production of wood materials, aminoplast resins can be used. Such resins and their preparation, for example, in Ullmann's Encyclopedia of Industrial Chemistry, 4th, revised and expanded edition, Verlag Chemie, 1973, pages 403 to 424 "aminoplasts" and Ullmann's Encyclopedia of Industrial
- Preferred aminoplast resins are polycondensation products of compounds having at least one carbamide group and formaldehyde, which are also partially substituted by organic radicals.
- aminoplast resins are urea-formaldehyde resins (UF resins), melamine-formaldehyde resins (MF resins) or melamine-containing urea-formaldehyde resins (MUF resins).
- UF resins urea-formaldehyde resins
- MF resins melamine-formaldehyde resins
- UMF resins melamine-containing urea-formaldehyde resins
- urea-formaldehyde resins for example Kaurit ® glue types from BASF Aktiengesellschaft.
- very preferred aminoplast resins are polycondensation products of compounds having at least one, also partially substituted by organic radicals, amino group and aldehyde, wherein the molar ratio of aldehyde: optionally partially substituted with organic radicals amino group in the range of 0.3 to 1, 0 preferred 0.3 to 0.60, more preferably 0.3 to 0.45, most preferably 0.30 to 0.40.
- very preferred aminoplast resins are polycondensation products of compounds having at least one amino group -NH 2 and formaldehyde, wherein the molar ratio of formaldehyde: -NH 2 group in the range of 0.3 to 1, preferably 0.3 to 0.60, particularly preferred 0.3 to 0.45, most preferably 0.30 to 0.40.
- aminoplast resins are urea-formaldehyde resins (UF resins), melamine-formaldehyde resins (MF resins) or melamine-containing urea-formaldehyde resins (MUF resins), wherein the molar ratio of formaldehyde: -NH 2 group in the range of 0.3 to 1, 0, preferably 0.3 to 0.60, particularly preferably 0.3 to 0.45, very particularly preferably 0.30 to 0.40.
- UF resins urea-formaldehyde resins
- MF resins melamine-formaldehyde resins
- MMF resins melamine-containing urea-formaldehyde resins
- very preferred aminoplast resins are urea-formaldehyde resins (UF resins), wherein the molar ratio of formaldehyde: -NH2 group in the range of 0.3 to 1, preferably 0.3 to 0.60, particularly preferably 0.3 to 0.45, most preferably 0.30 to 0.40.
- UF resins urea-formaldehyde resins
- the aminoplast resins mentioned are usually suspended in liquid form, usually in a liquid suspending agent or dissolved, preferably in aqueous suspension or solution, but can also be used as a solid.
- the solids content of the aminoplast resin suspensions, preferably aqueous suspension is usually from 25 to 90% by weight, preferably from 50 to 70% by weight.
- the solids content of the aminoplast resin in aqueous suspension can be determined according to Günter Zeppenfeld, Dirk Grunwald, adhesives in the wood and furniture industry, 2nd edition, DRW-Verlag, page 268.
- To determine the solids content of aminoplast glues 1 g of amino resin glue is accurately weighed in a weighing dish, finely dispersed on the ground and dried in a drying oven for 2 hours at 120 0 C. After tempering to room temperature in a desiccator, the residue is weighed and calculated as a percentage of the initial weight.
- the aminoplast resins are prepared by known processes (see above Ullman literature “aminoplasts” and “Amino Resins”, as well as above-mentioned literature Dunky et al.) By reacting the carbamido-containing compounds, preferably urea and / or melamine, with the Aldehydes, preferably formaldehyde, in the desired molar ratios of carbamide group: aldehyde, preferably in water as solvent.
- aldehyde preferably formaldehyde: optionally partially substituted with organic radicals amino group
- NH 2 group-carrying monomers are preferably urea, melamine, more preferably urea.
- the total amount of the binder C), based on the light wood-containing substance is in the range from 0.1 to 50% by weight, preferably 0.5 to 15% by weight, particularly preferably 0.5 to 10% by weight. ,
- the total amount of the aminoplast resin (always based on the solid), preferably the urea-formaldehyde resin and / or melamine-urea-formaldehyde resin and / or melamine-formaldehyde resin, more preferably urea-formaldehyde resin, in the binder C), based on the light holzhalti - Gen fabric in the range of 1 to 45 wt .-%, preferably 4 to 14 wt .-%, particularly preferably 6 to 9 wt .-%.
- an organic isocyanate is a single or further constituent of the binder C
- the total amount of the organic isocyanate preferably of the oligomeric isocyanate having 2 to 10, preferably 2 to 8 monomer units and an average of at least one isocyanate group per monomer unit, more preferably PMDI, in the binder C), based on the light wood-containing substance in the range of 0.1 to 5% by weight, preferably 0.25 to 3.5 wt .-%, particularly preferably 0.5 to 1, 5 wt .-%.
- Preferred embodiments of the light wood-containing material contain (i) 55 to 92.5 wt .-%, preferably 60 to 90 wt .-%, in particular 70 to 88 wt .-%, based on the light wood-containing material, wood particles A), wherein the wood particles A) have an average density of 0.4 to 0.85 g / cm 3 , preferably 0.4 to 0.75 g / cm 3 , in particular 0.4 to 0.6 g / cm 3 ; (Ii) 1 to 25 wt .-%, preferably 2 to 15 wt .-%, in particular 3 to 12 wt .-% based on the light wood-containing material, polystyrene and / or styrene copolymer filler B), wherein the filler B ) has a bulk density of 10 to 150 kg / m 3 , preferably 20 to 80 kg / m 3 , in particular 30 to 60 kg / m 3 and wherein the filler B)
- component D) in the light wood-containing substance or multilayer wood material according to the invention for example water repellents, such as paraffin emulsions, antifungal agents and flame retardants.
- the present invention further relates to a multilayer wood material containing at least three layers of wood material, at least the middle layer (s) containing or containing a light wood-containing material having the following characteristics of the light wood-containing material: an average density in the range of 200 to 600 kg / m 3 and containing, in each case based on the light wood-containing substance
- component B) contains plasticized particles obtained by comminution of shaped bodies in an amount, based on component B), in the range from 1% by weight to 100% by weight.
- the average density of the multilayer, preferably of the three-layer, wood material according to the invention is in the range of 300 kg / m 3 to 600 kg / m 3 , preferably in the range of 350 kg / m 3 to 600 kg / m 3 , particularly preferably in the range of 400 kg / m 3 to 500 kg / m 3 .
- Middle layers in the sense of the invention are all layers that are not the outer layers.
- the outer layers (usually called “cover layer (s)" have no fillers.
- the multilayer wood material according to the invention contains three layers of wood pulp, wherein the outer cover layers together make up 1 to 25% of the total thickness of the multilayer wood material according to the invention, preferably 3 to 20%, in particular 5 to 15%.
- the binder used for the outer layers is usually an aminoplast resin, for example urea-formaldehyde resin (UF), melamine-formaldehyde resin (MF), melamine-urea-formaldehyde resin (MUF) or the binder C according to the invention.
- the binder used for the outer layers is an aminoplast resin, more preferably a urea-formaldehyde resin, most preferably an aminoplast resin wherein the molar formaldehyde: -N ⁇ group ratio is in the range of 0.3 to 1.0.
- the thickness of the multilayer wood material according to the invention varies with the field of application and is generally in the range of 0.5 to 100 mm; preferably in the range of 10 to 40 mm, in particular 15 to 20 mm.
- the present invention relates to a method for producing multilayer wood-based materials according to the invention as defined above, wherein the components for the individual layers are stacked and pressed under elevated temperature and elevated pressure.
- the processes for producing multilayer wood-based materials are known in principle and described, for example, in M. Dunky, P. Niemz, Holzwerkstoffe und Glue, Springer 2002, pages 91 to 150.
- the chips After cutting the wood, the chips are dried. Thereafter, if necessary, coarse and fines are removed. The remaining chips are sorted by sieving or sifting in the air stream.
- the coarser material is used for the middle layer, the coarser material for the cover layers.
- Middle layer and outer layer chips are glued separately from each other with the components B) (only the middle layers)), C) (middle layer) and optionally D) (middle layer and / or outer layers) and with an aminoplast resin (top layer), or mixed and then scattered , First, the cover layer material is scattered on the forming belt, then the middle layer material - containing the components B), C) and optionally D) - and finally once more cover layer material.
- the three-layer chip cake thus produced is precompressed cold (usually at room temperature) and then pressed hot.
- the pressing can be carried out by all methods known to the person skilled in the art. Usually, the wood particle cake is pressed at a press temperature of 150 0 C to 230 0 C to the desired thickness.
- the pressing time is normally 3 to 15 seconds per mm plate thickness. This gives a three-layer chipboard.
- Preferred parameter ranges and preferred embodiments with regard to the average density of the light wood-containing material, the multilayer wood-based material and with regard to the components A), B), C) and optionally D) and the combination of the features correspond to those described above.
- the prefoamed or non-prefoamed polystyrene and / or styrene copolymer is provided with an antistatic coating prior to mixing with the binder and / or the wood particles.
- an antistatic coating the above applies.
- the present invention relates to the use of the light wood-containing material according to the invention and the multilayer wood material according to the invention for the production of objects of all kinds, for example furniture, furniture parts or packaging materials, the use of light wood-containing material according to the invention and the multilayer wood material according to the invention in the building rich.
- items of all kinds include furniture, furniture parts and packaging materials, wall and ceiling panels, doors and floors.
- furniture or furniture parts are kitchen furniture, cabinets, chairs, tables, countertops, for example for kitchen furniture, desk tops.
- packaging materials are boxes, boxes.
- Examples of the construction sector are structural engineering, civil engineering, interior construction, tunneling, where the wood-containing materials or multilayer wood-based materials according to the invention can be used as shuttering panels or as a carrier.
- the advantages of the present invention lie in the low density of the light wood-containing material or multilayer wood material according to the invention, wherein a good mechanical stability is maintained.
- the wood-containing material according to the invention or the multilayer wood-based material according to the invention exhibits good transverse tensile values in conjunction with good flexural strength values.
- the light wood-containing material and multi-layer wood material according to the invention can be easily produced; there is no need to retrofit the existing plants for the production of the multilayer wood-based materials according to the invention.
- the Bekant zucchini the light wood-containing materials according to the invention or especially of the multilayer wood materials adheres particularly well and is not uneven or wavy, the narrow surface, in particular of the multilayer wood material, is not characterized by the edge through, the edge is pressure-stable and edging can be done with the usual machines of plate making and edging.
- the swelling values of the multilayer wood-base materials according to the invention are advantageously 10% smaller, preferably 20% smaller, in particular 30% smaller than the swelling values of an analogous plate of the same density without filler.
- Neopor ® N2200 (neopor ® is a commercial product and trademark of BASF Aktiengesellschaft) was treated with steam in a continuous prefoamer.
- the bulk density of 50 kg / m 3 of the pre-expanded polystyrene beads was adjusted by varying the vapor pressure and the steaming time.
- the average particle diameter after pre-foaming was 1, 9 to 2.5 mm. A2) By crushing of shaped bodies
- a polystyrene foam block which was used as packaging material and has a density of 20 kg / m 3 , was milled in a Pallmann impact mill type PP to an average particle diameter of 1 to 2 mm.
- a Neopor ® foam block which has been used as an insulating material, and a density of 20 kg / m 3, was ground in an impact mill Pallmann type PP to an average particle diameter of 1 to 2 mm.
- glues was urea-formaldehyde glue (glue Kaurit ® 340 from BASF Aktiengesellschaft) were used. The solids content was adjusted in each case with water to 67 wt .-%. For details see also in the table.
- a mixer 450 g of chips (component A)) were mixed according to the table and optionally component B) according to the table. Subsequently, 58.8 g of a glue liquor comprising 100 parts Kaurit ® -Leim 340 and 4 parts of a 52% aqueous ammonium nitrate solution and 10 parts of water were applied.
- the glued chips were cold pre-compacted in a 30x30cm-form.
- the mixture was then pressed in a hot press (press temperature 190 0 C, pressing time 210 s).
- the nominal thickness of the plate was 16mm in each case.
- the density was determined 24 hours after preparation according to DIN EN 1058.
- the determination of the bending strength was carried out according to DIN EN 310.
- the quantities always refer to the dry matter.
- the dry wood or the sum of the dry wood and the filler is set to 100 parts.
- the wt .-% the sum of all dry constituents of the light wood-containing substance is equal to 100%.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Wood Science & Technology (AREA)
- Forests & Forestry (AREA)
- Dry Formation Of Fiberboard And The Like (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
- Laminated Bodies (AREA)
- Rod-Shaped Construction Members (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL07821531T PL2083975T3 (pl) | 2006-10-19 | 2007-10-18 | Lekkie tworzywa drzewne o dobrych właściwościach mechanicznych i sposób ich wytwarzania |
| EP20070821531 EP2083975B1 (fr) | 2006-10-19 | 2007-10-18 | Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques et leur methode de production |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06122557.9A EP1914052B1 (fr) | 2006-10-19 | 2006-10-19 | Materiau léger a base de bois |
| EP20070821531 EP2083975B1 (fr) | 2006-10-19 | 2007-10-18 | Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques et leur methode de production |
| PCT/EP2007/061166 WO2008046891A1 (fr) | 2006-10-19 | 2007-10-18 | Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2083975A1 true EP2083975A1 (fr) | 2009-08-05 |
| EP2083975B1 EP2083975B1 (fr) | 2010-12-29 |
Family
ID=37311395
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP06122557.9A Active EP1914052B1 (fr) | 2006-10-19 | 2006-10-19 | Materiau léger a base de bois |
| EP07821532A Withdrawn EP2083976A2 (fr) | 2006-10-19 | 2007-10-18 | Materiau leger a base de bois |
| EP20070821531 Active EP2083975B1 (fr) | 2006-10-19 | 2007-10-18 | Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques et leur methode de production |
| EP07821530.8A Active EP2083974B1 (fr) | 2006-10-19 | 2007-10-18 | Materiau leger a base de bois |
| EP20110152229 Withdrawn EP2319670A1 (fr) | 2006-10-19 | 2007-10-18 | Matériau léger à base de bois |
Family Applications Before (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP06122557.9A Active EP1914052B1 (fr) | 2006-10-19 | 2006-10-19 | Materiau léger a base de bois |
| EP07821532A Withdrawn EP2083976A2 (fr) | 2006-10-19 | 2007-10-18 | Materiau leger a base de bois |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP07821530.8A Active EP2083974B1 (fr) | 2006-10-19 | 2007-10-18 | Materiau leger a base de bois |
| EP20110152229 Withdrawn EP2319670A1 (fr) | 2006-10-19 | 2007-10-18 | Matériau léger à base de bois |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US9089991B2 (fr) |
| EP (5) | EP1914052B1 (fr) |
| JP (2) | JP5300728B2 (fr) |
| CN (2) | CN101553348B (fr) |
| AT (1) | ATE493247T1 (fr) |
| AU (2) | AU2007312220B2 (fr) |
| BR (2) | BRPI0717434A2 (fr) |
| CA (2) | CA2666454A1 (fr) |
| DE (2) | DE202006020503U1 (fr) |
| EA (2) | EA013666B1 (fr) |
| ES (3) | ES2641263T3 (fr) |
| MY (2) | MY148871A (fr) |
| NO (3) | NO20091516L (fr) |
| NZ (2) | NZ576323A (fr) |
| PL (3) | PL1914052T3 (fr) |
| PT (3) | PT1914052T (fr) |
| UA (2) | UA96612C2 (fr) |
| WO (3) | WO2008046891A1 (fr) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0706437A2 (pt) * | 2006-01-17 | 2011-03-29 | Basf Se | processo para a redução da emissão de formaldeìdo de material à base de madeiras, material à base de madeira, laminado, e, uso do material à base de madeira |
| PT1914052T (pt) | 2006-10-19 | 2017-10-04 | Basf Se | Materiais leves à base de madeira |
| BE1017821A5 (nl) * | 2007-10-19 | 2009-08-04 | Flooring Ind Ltd Sarl | Plaat, werkwijzen voor het vervaardigen van platen en paneel dat dergelijk plaatmateriaal bevat. |
| CL2008003701A1 (es) | 2008-01-11 | 2009-05-08 | Nova Chem Inc | Método para producir un artículo de material compuesto espumado de fibra celulósica-termoplástico. |
| EP2172333A1 (fr) * | 2008-09-19 | 2010-04-07 | Basf Se | Corps de formage à teneur en lignocellulose multicouche à émission en formaldéhyde réduite |
| PL2223786T3 (pl) | 2009-02-26 | 2015-02-27 | SWISS KRONO Tec AG | Płyta z tworzywa drzewnego oraz sposób wytwarzania płyty z tworzywa drzewnego |
| GB0908487D0 (en) * | 2009-05-18 | 2009-06-24 | Dynea Oy | Resin system for foam core boards |
| US20120138224A1 (en) * | 2009-08-13 | 2012-06-07 | Basf Se | Light lignocellulose materials having good mechanical properties |
| NZ598089A (en) * | 2009-08-13 | 2013-03-28 | Basf Se | Light lignocellulosic materials having good mechanical properties |
| CA2779362A1 (fr) * | 2009-11-06 | 2011-05-12 | Basf Se | Materiaux lignocellulosiques presentant de bonnes proprietes mecaniques |
| DE102009056843A1 (de) | 2009-12-02 | 2011-06-09 | Michanickl, Andreas, Prof.Dr. | Leichte Holzwerkstoffplatte |
| US8920923B2 (en) | 2010-03-04 | 2014-12-30 | Basf Se | Lignocellulose materials having good mechanical properties |
| US8623501B2 (en) | 2010-03-04 | 2014-01-07 | Basf Se | Lignocellulose materials having good mechanical properties |
| EP2542625A4 (fr) * | 2010-03-04 | 2013-10-23 | Basf Se | Matériaux lignocellulosiques présentant des propriétés mécaniques satisfaisantes |
| WO2012080338A1 (fr) | 2010-12-17 | 2012-06-21 | Basf Se | Corps moulé multicouche contenant de la lignocellulose, avec une faible émission de formaldéhyde |
| CN102020862B (zh) * | 2011-01-07 | 2012-04-25 | 福建农林大学 | 一种轻质木塑复合材料及其制造方法 |
| CN103112071B (zh) * | 2011-11-17 | 2015-09-16 | 上海通用汽车有限公司 | 汽车内饰件及其制造方法 |
| DE102011056946A1 (de) | 2011-12-22 | 2013-06-27 | Nolte Holzwerkstoff Gmbh & Co. Kg | Gewichtsreduzierte Spanplatte mit mechanisch belastbarer Polystyrol-Einlage |
| US9266308B2 (en) * | 2011-12-23 | 2016-02-23 | Basf Se | Lignocellulosic materials with expanded plastics particles present in nonuniform distribution in the core |
| JP6173343B2 (ja) * | 2011-12-23 | 2017-08-02 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 不均一にコア中に分布して存在する発泡プラスチック粒子を有するリグノセルロース材料 |
| SI2794211T1 (sl) * | 2011-12-23 | 2016-09-30 | Basf Se | Lignocelulozni materiali z lignoceluloznimi vlakni v zunanjih plasteh in ekspandiranimi delci plastike, prisotni v jedru ter procesi in njihova uporaba |
| PL3024669T3 (pl) | 2013-07-22 | 2018-12-31 | Akzenta Paneele + Profile Gmbh | Sposób wytwarzania dekorowanego panelu ściennego lub podłogowego |
| WO2015048441A1 (fr) | 2013-09-30 | 2015-04-02 | Basf Se | Articles composites lignocellulosiques |
| CN103568097A (zh) * | 2013-10-21 | 2014-02-12 | 黄宣斐 | 一种含有天然木纤维的低密度板 |
| EP2942208A1 (fr) * | 2014-05-09 | 2015-11-11 | Akzenta Paneele + Profile GmbH | Procédé de fabrication d'un panneau mural ou de sol décoré |
| CN104786342A (zh) * | 2015-04-24 | 2015-07-22 | 东北林业大学 | 低密度“三明治”结构的木质复合板材及其制备方法 |
| CN105150352A (zh) * | 2015-10-14 | 2015-12-16 | 中山冠华竹纤板业有限公司 | 一种调质养生竹纤维板及其生产工艺 |
| US11065847B2 (en) * | 2016-02-23 | 2021-07-20 | Financiera Maderera, S.A. | Method for the production of multilayer laminated board and resulting board |
| CN105754363A (zh) * | 2016-03-15 | 2016-07-13 | 南通长城装饰木制品制造有限公司 | 一种具有甲醛净化功能的纤维木材及其制备方法 |
| US12157250B2 (en) * | 2016-03-21 | 2024-12-03 | Bondcore öU | Composite wood panels with corrugated cores and method of manufacturing same |
| TWI778957B (zh) * | 2016-03-30 | 2022-10-01 | 大陸商贏創特種化學(上海)有限公司 | 包含聚(甲基)丙烯醯亞胺發泡體粒子的聚合物混合物 |
| MX2019000173A (es) * | 2016-07-06 | 2019-09-26 | Sonoco Dev Inc | Carrete hecho de componentes moldeados. |
| CN107150382A (zh) * | 2017-01-11 | 2017-09-12 | 廖伟登 | 松柏桉混合制成的建筑用层压板 |
| US20210253861A1 (en) | 2018-08-28 | 2021-08-19 | Basf Se | Lignocellulosic composite articles |
| EP3938415A1 (fr) | 2019-03-15 | 2022-01-19 | Basf Se | Articles composites lignocellulosiques |
| PT115374A (pt) | 2019-03-15 | 2020-10-08 | Univ Do Porto | Compósitos de baixa densidade de poliuretano-madeira e o seu método de fabrico |
| CN111168803A (zh) * | 2019-12-31 | 2020-05-19 | 嘉兴市集美新材料科技有限公司 | 环保防水高强度的人造板及其制造方法 |
| CN112497413A (zh) * | 2020-11-29 | 2021-03-16 | 千年舟新材科技集团股份有限公司 | 一种发泡材料、超低密度的阻燃定向刨花板及制备方法 |
| CN113801492B (zh) * | 2021-09-24 | 2023-08-25 | 湖南兆恒材料科技有限公司 | 一种吸波复合泡沫材料及其制备方法 |
| WO2024008938A1 (fr) | 2022-07-08 | 2024-01-11 | Covestro (Netherlands) B.V. | Compositions pour panneaux de fibres présentant des propriétés améliorées lors d'un durcissement rapide à basse température |
| CN119497731A (zh) | 2022-07-08 | 2025-02-21 | 科思创(荷兰)有限公司 | 用于在低温下快速固化后具有增强的性质的纤维板的组合物 |
| CN119497664A (zh) | 2022-07-08 | 2025-02-21 | 科思创(荷兰)有限公司 | 用于在低温下快速固化后具有增强的性质的纤维板的组合物 |
| EP4572932A1 (fr) | 2022-08-19 | 2025-06-25 | Covestro (Netherlands) B.V. | Compositions pour panneaux de fibres présentant des propriétés améliorées lors d'un durcissement rapide à basse température |
| CN119731270A (zh) | 2022-08-19 | 2025-03-28 | 科思创(荷兰)有限公司 | 用于在低温下快速固化后具有增强的性质的纤维板的组合物 |
| WO2025036666A1 (fr) | 2023-08-17 | 2025-02-20 | Covestro (Netherlands) B.V. | Compositions pour panneaux de fibres présentant des propriétés améliorées lors d'un durcissement rapide à basse température |
Family Cites Families (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE370229C (de) * | 1923-03-01 | Ludwig Thallmayer | Verfahren zum Puffern von Wechselstromnetzen mittels Schwungrades | |
| DE845264C (de) | 1950-02-28 | 1952-08-14 | Basf Ag | Verfahren zur Herstellung poroeser Massen aus Polymerisaten |
| US2898632A (en) * | 1955-10-19 | 1959-08-11 | Dayton Formold Inc | Molding plastic foam |
| DE1192402B (de) * | 1956-12-17 | 1965-05-06 | Max Himmelheber Dipl Ing | Verfahren zur Herstellung von Spanplatten und Spanholzkoerpern vornehmlich niedrigen spezifischen Gewichts |
| US3963816A (en) * | 1971-09-02 | 1976-06-15 | Foster Grant Co., Inc. | Process for molding expandable thermoplastic material |
| JPS5445385A (en) * | 1977-09-17 | 1979-04-10 | Nippon Musical Instruments Mfg | Particle board |
| DE3234660C2 (de) | 1982-09-18 | 1984-07-19 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von teilchenförmigen,treibmittelhaltigen Styrolpolymerisaten |
| JPS5989136A (ja) * | 1982-11-15 | 1984-05-23 | Toshiba Mach Co Ltd | スチレン系ポリマ−の溶融押出方法 |
| JPH0631708B2 (ja) | 1985-02-08 | 1994-04-27 | 株式会社日立製作所 | 蓄熱装置 |
| JPH02220808A (ja) * | 1989-02-23 | 1990-09-04 | Nippon Kasei Kk | 導電性木質繊維成形板 |
| DE3921148A1 (de) * | 1989-06-28 | 1991-01-10 | Basf Ag | Perlfoermige expandierbare styrolpolymerisate mit hohem expandiervermoegen |
| US5002713A (en) * | 1989-12-22 | 1991-03-26 | Board Of Control Of Michigan Technological University | Method for compression molding articles from lignocellulosic materials |
| JPH0631708A (ja) * | 1992-07-20 | 1994-02-08 | Okura Ind Co Ltd | 軽量パーティクルボード |
| NZ260980A (en) * | 1993-07-14 | 1996-08-27 | Yamaha Corp | Wood board; core layer of wooden strips & foaming binder and surface layer of oriented strand board with wooden strips & binder |
| JPH07144308A (ja) * | 1993-11-22 | 1995-06-06 | Yamaha Corp | 表面化粧木質板 |
| CN1099328A (zh) * | 1994-03-16 | 1995-03-01 | 郭柏林 | 一种轻质刨花板的生产工艺及其产品 |
| CN2244987Y (zh) * | 1996-05-21 | 1997-01-15 | 赵凤岐 | 人造复合板 |
| DE59702327D1 (de) * | 1997-05-14 | 2000-10-12 | Basf Ag | Graphitpartikel enthaltende expandierbare styrolpolymerisate |
| JP2001191308A (ja) * | 2000-01-12 | 2001-07-17 | Pan Techno:Kk | 木屑の有効利用法 |
| JP2001287231A (ja) * | 2000-04-07 | 2001-10-16 | Nichiha Corp | 木質成形体およびその製造方法 |
| AU2002214183A1 (en) * | 2000-11-10 | 2002-05-21 | Symons, Michael Windsor | Method of making a finished product |
| EP1271844B1 (fr) | 2001-06-21 | 2009-12-09 | SK Telecom Co.,Ltd. | Procédé pour déterminer une route dans un réseau à commutation d'étiquettes multiprotocole |
| JP2003039410A (ja) * | 2001-07-27 | 2003-02-13 | Togiya:Kk | 樹脂強化木材製品およびその製造方法 |
| US7217458B2 (en) * | 2003-07-16 | 2007-05-15 | Huber Engineered Woods Llc | Strength-enhanced, lightweight lignocellulosic composite board materials and methods of their manufacture |
| CN1274765C (zh) * | 2004-11-18 | 2006-09-13 | 中国科学院广州化学研究所 | 一种甘蔗渣和聚苯乙烯共混人造纤维制品的制造方法 |
| JP5258147B2 (ja) * | 2005-01-28 | 2013-08-07 | 積水化成品工業株式会社 | 発泡性熱可塑性樹脂粒子とその製造方法、発泡性熱可塑性樹脂粒子用帯電防止剤組成物及び発泡性熱可塑性樹脂粒子の帯電防止方法 |
| BRPI0706437A2 (pt) * | 2006-01-17 | 2011-03-29 | Basf Se | processo para a redução da emissão de formaldeìdo de material à base de madeiras, material à base de madeira, laminado, e, uso do material à base de madeira |
| PT1914052T (pt) * | 2006-10-19 | 2017-10-04 | Basf Se | Materiais leves à base de madeira |
| EP2042560A1 (fr) * | 2007-09-19 | 2009-04-01 | Basf Se | Matériaux légers dérivés du bois dotés de bonnes propriétés mécaniques et d'émissions réduites de formaldéhyde |
| ITMO20080070A1 (it) * | 2008-03-11 | 2009-09-12 | Massimiliano Pineschi | Bevanda - condimento |
-
2006
- 2006-10-19 PT PT61225579T patent/PT1914052T/pt unknown
- 2006-10-19 EP EP06122557.9A patent/EP1914052B1/fr active Active
- 2006-10-19 ES ES06122557.9T patent/ES2641263T3/es active Active
- 2006-10-19 PL PL06122557T patent/PL1914052T3/pl unknown
- 2006-10-19 DE DE200620020503 patent/DE202006020503U1/de not_active Expired - Lifetime
-
2007
- 2007-10-18 BR BRPI0717434-9A2A patent/BRPI0717434A2/pt not_active IP Right Cessation
- 2007-10-18 MY MYPI20091588A patent/MY148871A/en unknown
- 2007-10-18 BR BRPI0717436-5A2A patent/BRPI0717436A2/pt not_active IP Right Cessation
- 2007-10-18 ES ES07821531T patent/ES2357574T3/es active Active
- 2007-10-18 CA CA 2666454 patent/CA2666454A1/fr not_active Abandoned
- 2007-10-18 US US12/446,248 patent/US9089991B2/en not_active Expired - Fee Related
- 2007-10-18 AU AU2007312220A patent/AU2007312220B2/en not_active Ceased
- 2007-10-18 MY MYPI20091585A patent/MY148865A/en unknown
- 2007-10-18 EP EP07821532A patent/EP2083976A2/fr not_active Withdrawn
- 2007-10-18 PL PL07821531T patent/PL2083975T3/pl unknown
- 2007-10-18 NZ NZ576323A patent/NZ576323A/en not_active IP Right Cessation
- 2007-10-18 DE DE200750006137 patent/DE502007006137D1/de active Active
- 2007-10-18 PT PT07821531T patent/PT2083975E/pt unknown
- 2007-10-18 EP EP20070821531 patent/EP2083975B1/fr active Active
- 2007-10-18 EA EA200900551A patent/EA013666B1/ru not_active IP Right Cessation
- 2007-10-18 ES ES07821530.8T patent/ES2622883T3/es active Active
- 2007-10-18 WO PCT/EP2007/061166 patent/WO2008046891A1/fr not_active Ceased
- 2007-10-18 CA CA 2666447 patent/CA2666447A1/fr not_active Abandoned
- 2007-10-18 JP JP2009532808A patent/JP5300728B2/ja not_active Expired - Fee Related
- 2007-10-18 US US12/446,245 patent/US8304069B2/en not_active Expired - Fee Related
- 2007-10-18 UA UAA200904960A patent/UA96612C2/ru unknown
- 2007-10-18 CN CN2007800428544A patent/CN101553348B/zh not_active Expired - Fee Related
- 2007-10-18 PL PL07821530T patent/PL2083974T3/pl unknown
- 2007-10-18 EA EA200900550A patent/EA013665B1/ru not_active IP Right Cessation
- 2007-10-18 PT PT78215308T patent/PT2083974T/pt unknown
- 2007-10-18 EP EP07821530.8A patent/EP2083974B1/fr active Active
- 2007-10-18 EP EP20110152229 patent/EP2319670A1/fr not_active Withdrawn
- 2007-10-18 AU AU2007312218A patent/AU2007312218B2/en not_active Ceased
- 2007-10-18 JP JP2009532809A patent/JP5150638B2/ja not_active Expired - Fee Related
- 2007-10-18 WO PCT/EP2007/061167 patent/WO2008046892A2/fr not_active Ceased
- 2007-10-18 AT AT07821531T patent/ATE493247T1/de active
- 2007-10-18 CN CN200780042908.7A patent/CN101541488B/zh not_active Expired - Fee Related
- 2007-10-18 UA UAA200904962A patent/UA94123C2/ru unknown
- 2007-10-18 NZ NZ576290A patent/NZ576290A/en not_active IP Right Cessation
- 2007-10-18 WO PCT/EP2007/061165 patent/WO2008046890A2/fr not_active Ceased
-
2009
- 2009-04-17 NO NO20091516A patent/NO20091516L/no not_active Application Discontinuation
- 2009-04-17 NO NO20091522A patent/NO20091522L/no not_active Application Discontinuation
- 2009-04-17 NO NO20091523A patent/NO20091523L/no not_active Application Discontinuation
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2008046891A1 * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2083975B1 (fr) | Matériaux légers dérivés du bois présentant de bonnes propriétés mécaniques et leur methode de production | |
| EP2193170B1 (fr) | Matériau léger à base de bois à bonnes propriétés mécaniques et faible émission de formaldéhyde | |
| EP2464691A1 (fr) | Matériaux lignocellulosiques légers présentant de bonnes propriétés mécaniques | |
| EP2464692A1 (fr) | Matériaux lignocellulosiques légers possédant de bonnes propriétés mécaniques | |
| EP2496647A1 (fr) | Matériaux lignocellulosiques présentant de bonnes propriétés mécaniques |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
| 17P | Request for examination filed |
Effective date: 20090519 |
|
| AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: HR RS |
|
| 17Q | First examination report despatched |
Effective date: 20091030 |
|
| RAX | Requested extension states of the european patent have changed |
Extension state: HR Payment date: 20090519 Extension state: RS Payment date: 20090519 |
|
| GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
| RTI1 | Title (correction) |
Free format text: LIGHT WOOD MATERIALS WITH GOOD MECHANICAL CHARACTERISTICS AND METHOD OF PRODUCING THE SAME |
|
| GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
| GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
| AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR |
|
| AX | Request for extension of the european patent |
Extension state: HR RS |
|
| REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D Free format text: NOT ENGLISH |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: LANGUAGE OF EP DOCUMENT: GERMAN |
|
| REG | Reference to a national code |
Ref country code: PT Ref legal event code: SC4A Free format text: AVAILABILITY OF NATIONAL TRANSLATION Effective date: 20110127 |
|
| REF | Corresponds to: |
Ref document number: 502007006137 Country of ref document: DE Date of ref document: 20110210 Kind code of ref document: P |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 502007006137 Country of ref document: DE Effective date: 20110210 |
|
| REG | Reference to a national code |
Ref country code: NL Ref legal event code: VDEP Effective date: 20101229 Ref country code: ES Ref legal event code: FG2A Ref document number: 2357574 Country of ref document: ES Kind code of ref document: T3 Effective date: 20110427 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| LTIE | Lt: invalidation of european patent or patent extension |
Effective date: 20101229 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20110329 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| REG | Reference to a national code |
Ref country code: PL Ref legal event code: T3 |
|
| REG | Reference to a national code |
Ref country code: IE Ref legal event code: FD4D |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20110429 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20110330 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| PLBI | Opposition filed |
Free format text: ORIGINAL CODE: 0009260 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| 26 | Opposition filed |
Opponent name: FLOORING TECHNOLOGIES LTD. Effective date: 20110928 |
|
| PLAX | Notice of opposition and request to file observation + time limit sent |
Free format text: ORIGINAL CODE: EPIDOSNOBS2 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R026 Ref document number: 502007006137 Country of ref document: DE Effective date: 20110928 |
|
| PLBB | Reply of patent proprietor to notice(s) of opposition received |
Free format text: ORIGINAL CODE: EPIDOSNOBS3 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20111031 |
|
| REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20111031 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20111031 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| PLCK | Communication despatched that opposition was rejected |
Free format text: ORIGINAL CODE: EPIDOSNREJ1 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20111018 |
|
| PLBN | Opposition rejected |
Free format text: ORIGINAL CODE: 0009273 |
|
| STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: OPPOSITION REJECTED |
|
| 27O | Opposition rejected |
Effective date: 20130314 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20101229 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R100 Ref document number: 502007006137 Country of ref document: DE Effective date: 20130314 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: PL Payment date: 20140926 Year of fee payment: 8 Ref country code: TR Payment date: 20140929 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20141031 Year of fee payment: 8 Ref country code: ES Payment date: 20141127 Year of fee payment: 8 Ref country code: FR Payment date: 20141031 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 20141029 Year of fee payment: 8 Ref country code: PT Payment date: 20141013 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20141022 Year of fee payment: 8 |
|
| PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20141230 Year of fee payment: 8 Ref country code: BE Payment date: 20141030 Year of fee payment: 8 |
|
| REG | Reference to a national code |
Ref country code: PT Ref legal event code: MM4A Free format text: LAPSE DUE TO NON-PAYMENT OF FEES Effective date: 20160418 |
|
| REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 502007006137 Country of ref document: DE |
|
| REG | Reference to a national code |
Ref country code: AT Ref legal event code: MM01 Ref document number: 493247 Country of ref document: AT Kind code of ref document: T Effective date: 20151018 |
|
| GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20151018 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151018 Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151018 Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160503 |
|
| REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20160630 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151018 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151102 Ref country code: PT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20160418 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151018 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151019 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151031 |
|
| PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20151018 |
|
| REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20180706 |