DE102008058225A1 - Leichtbauteil in Hybridbauweise - Google Patents
Leichtbauteil in Hybridbauweise Download PDFInfo
- Publication number
- DE102008058225A1 DE102008058225A1 DE200810058225 DE102008058225A DE102008058225A1 DE 102008058225 A1 DE102008058225 A1 DE 102008058225A1 DE 200810058225 DE200810058225 DE 200810058225 DE 102008058225 A DE102008058225 A DE 102008058225A DE 102008058225 A1 DE102008058225 A1 DE 102008058225A1
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- polyamide
- thermoplastic
- oder
- Prior art date
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- CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
- 229960000367 inositol Drugs 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000013980 iron oxide Nutrition 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
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- 150000007517 lewis acids Chemical class 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
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- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 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
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- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
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- YSRVJVDFHZYRPA-UHFFFAOYSA-N melem Chemical compound NC1=NC(N23)=NC(N)=NC2=NC(N)=NC3=N1 YSRVJVDFHZYRPA-UHFFFAOYSA-N 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
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- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- CRVGTESFCCXCTH-UHFFFAOYSA-N methyl diethanolamine Chemical compound OCCN(C)CCO CRVGTESFCCXCTH-UHFFFAOYSA-N 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- ZIYVHBGGAOATLY-UHFFFAOYSA-N methylmalonic acid Chemical compound OC(=O)C(C)C(O)=O ZIYVHBGGAOATLY-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012170 montan wax Substances 0.000 description 1
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- 239000002105 nanoparticle Substances 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
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- 229910052756 noble gas Inorganic materials 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
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- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 150000002897 organic nitrogen compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
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- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005832 oxidative carbonylation reaction Methods 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- 210000000496 pancreas Anatomy 0.000 description 1
- WEAYWASEBDOLRG-UHFFFAOYSA-N pentane-1,2,5-triol Chemical compound OCCCC(O)CO WEAYWASEBDOLRG-UHFFFAOYSA-N 0.000 description 1
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 description 1
- RUOPINZRYMFPBF-UHFFFAOYSA-N pentane-1,3-diol Chemical compound CCC(O)CCO RUOPINZRYMFPBF-UHFFFAOYSA-N 0.000 description 1
- GLOBUAZSRIOKLN-UHFFFAOYSA-N pentane-1,4-diol Chemical compound CC(O)CCCO GLOBUAZSRIOKLN-UHFFFAOYSA-N 0.000 description 1
- XLMFDCKSFJWJTP-UHFFFAOYSA-N pentane-2,3-diol Chemical compound CCC(O)C(C)O XLMFDCKSFJWJTP-UHFFFAOYSA-N 0.000 description 1
- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000002979 perylenes Chemical class 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- CCDXIADKBDSBJU-UHFFFAOYSA-N phenylmethanetriol Chemical compound OC(O)(O)C1=CC=CC=C1 CCDXIADKBDSBJU-UHFFFAOYSA-N 0.000 description 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003007 phosphonic acid derivatives Chemical class 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- XZTOTRSSGPPNTB-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O XZTOTRSSGPPNTB-UHFFFAOYSA-N 0.000 description 1
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 1
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- HDOWRFHMPULYOA-UHFFFAOYSA-N piperidin-4-ol Chemical compound OC1CCNCC1 HDOWRFHMPULYOA-UHFFFAOYSA-N 0.000 description 1
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- 229920000573 polyethylene Polymers 0.000 description 1
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- 229920001721 polyimide Polymers 0.000 description 1
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- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
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- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 238000012958 reprocessing Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- WWYDYZMNFQIYPT-UHFFFAOYSA-N ru78191 Chemical compound OC(=O)C(C(O)=O)C1=CC=CC=C1 WWYDYZMNFQIYPT-UHFFFAOYSA-N 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000002109 single walled nanotube Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229940071182 stannate Drugs 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
- DYHSDKLCOJIUFX-UHFFFAOYSA-N tert-butoxycarbonyl anhydride Chemical compound CC(C)(C)OC(=O)OC(=O)OC(C)(C)C DYHSDKLCOJIUFX-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 238000007751 thermal spraying Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 150000003568 thioethers Chemical group 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical compound [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 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
- 238000005809 transesterification reaction Methods 0.000 description 1
- NFMWFGXCDDYTEG-UHFFFAOYSA-N trimagnesium;diborate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]B([O-])[O-].[O-]B([O-])[O-] NFMWFGXCDDYTEG-UHFFFAOYSA-N 0.000 description 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical compound O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- ZRQNRTRXAVFCMB-UHFFFAOYSA-N tris(2,4,5-trioxa-1-stanna-3-borabicyclo[1.1.1]pentan-1-yl) borate Chemical compound [Sn+4].[Sn+4].[Sn+4].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] ZRQNRTRXAVFCMB-UHFFFAOYSA-N 0.000 description 1
- GKODZWOPPOTFGA-UHFFFAOYSA-N tris(hydroxyethyl)aminomethane Chemical compound OCCC(N)(CCO)CCO GKODZWOPPOTFGA-UHFFFAOYSA-N 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- NSBGJRFJIJFMGW-UHFFFAOYSA-N trisodium;stiborate Chemical compound [Na+].[Na+].[Na+].[O-][Sb]([O-])([O-])=O NSBGJRFJIJFMGW-UHFFFAOYSA-N 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- GKXVJHDEWHKBFH-UHFFFAOYSA-N xylylenediamine group Chemical group C=1(C(=CC=CC1)CN)CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
- C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B62—LAND VEHICLES FOR TRAVELLING OTHERWISE THAN ON RAILS
- B62D—MOTOR VEHICLES; TRAILERS
- B62D29/00—Superstructures, understructures, or sub-units thereof, characterised by the material thereof
- B62D29/04—Superstructures, understructures, or sub-units thereof, characterised by the material thereof predominantly of synthetic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/08—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/18—Layered products comprising a layer of metal comprising iron or steel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/18—Layered products comprising a layer of synthetic resin characterised by the use of special additives
- B32B27/20—Layered products comprising a layer of synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
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Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
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| DE200810058225 DE102008058225A1 (de) | 2008-11-19 | 2008-11-19 | Leichtbauteil in Hybridbauweise |
| US12/617,927 US8383242B2 (en) | 2008-11-19 | 2009-11-13 | Lightweight component of hybrid |
| KR1020090111461A KR20100056402A (ko) | 2008-11-19 | 2009-11-18 | 혼성 경량 요소 |
| JP2009263130A JP2010120384A (ja) | 2008-11-19 | 2009-11-18 | ハイブリッドの軽量部材 |
| CN200910223652A CN101735603A (zh) | 2008-11-19 | 2009-11-19 | 混合的轻质部件 |
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| DE200810058225 DE102008058225A1 (de) | 2008-11-19 | 2008-11-19 | Leichtbauteil in Hybridbauweise |
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| DE102008058225A1 true DE102008058225A1 (de) | 2010-07-08 |
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| DE200810058225 Withdrawn DE102008058225A1 (de) | 2008-11-19 | 2008-11-19 | Leichtbauteil in Hybridbauweise |
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| US (1) | US8383242B2 (https=) |
| JP (1) | JP2010120384A (https=) |
| KR (1) | KR20100056402A (https=) |
| CN (1) | CN101735603A (https=) |
| DE (1) | DE102008058225A1 (https=) |
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| DE102011109471A1 (de) | 2011-08-04 | 2012-03-15 | Daimler Ag | Hybridbauteil für eine Karosserie eines Kraftwagens |
| FR2967936A1 (fr) * | 2010-11-25 | 2012-06-01 | Faurecia Bloc Avant | Procede de realisation d'une piece structurelle renforcee de vehicule automobile |
| WO2013001239A1 (fr) * | 2011-06-28 | 2013-01-03 | Renault S.A.S. | Dispositif de protection laterale pour vehicule automobile et vehicule automobile associe |
| DE102012012250A1 (de) * | 2012-02-10 | 2013-08-14 | Johnson Controls Gmbh | Fahrzeugsitz |
| DE102012111488A1 (de) | 2012-11-27 | 2014-05-28 | Thyssenkrupp Steel Europe Ag | Verfahren zum Herstellen eines Strukturbauteils, insbesondere für eine Karosserie |
| WO2015011422A1 (fr) * | 2013-07-25 | 2015-01-29 | Compagnie Plastic Omnium | Montant latéral pour caisse de véhicule automobile perfectionné |
| DE102014104475A1 (de) * | 2014-03-31 | 2015-10-01 | Volkswagen Ag | Kunststoff-Metall-Hybridbauteil und Verfahren zur Herstellung desselben |
| DE102015016259A1 (de) | 2015-12-15 | 2017-06-22 | INPRO Innovationsgesellschaft für fortgeschrittene Produktionssysteme in der Fahrzeugindustrie mbH | Verfahren zum Herstellen eines Kunststoff-Metall-Hybridbauteils |
| DE102017006863A1 (de) | 2017-07-19 | 2019-01-24 | INPRO Innovationsgesellschaft für fortgeschrittene Produktionssysteme in der Fahrzeugindustrie mbH | Verfahren zur inline-Herstellung eines Leichtbauteils in Hybridbauweise wie einer mit hybriden Strukturen zu versehenen Fahrzeugkarosserie |
| DE102017216840A1 (de) | 2017-09-22 | 2019-03-28 | Ford Global Technologies, Llc | Motorhaube aus Kunststoffmaterial mit wenigstens einem integrierten Funktionselement |
| CN112139356A (zh) * | 2020-09-18 | 2020-12-29 | 苏州邦得新材料科技有限公司 | 钢质金属印花编织板的制作的方法、钢质金属印花编织板 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| DE102006020984A1 (de) * | 2006-05-04 | 2007-11-08 | Lanxess Deutschland Gmbh | Leichtbauteil in Hybridbauweise |
| DE102008017977A1 (de) * | 2008-04-09 | 2009-10-15 | Daimler Ag | Leichtbauteil für eine Fahrzeugkarosserie |
| DE102009052110A1 (de) * | 2009-11-05 | 2011-05-12 | Faurecia Innenraum Systeme Gmbh | Kraftfahrzeug-Frontend |
| CN102933431B (zh) * | 2010-05-28 | 2016-03-16 | 京洛株式会社 | 冲击吸收体 |
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| KR101438783B1 (ko) * | 2012-12-28 | 2014-09-15 | 주식회사 포스코 | 자동차의 루프모듈 고정 구조 |
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| CN106458131A (zh) | 2014-06-16 | 2017-02-22 | 沙特基础工业全球技术有限公司 | 制备层压板的方法、吸能装置、吸能装置组合物及成形工具 |
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| JP7156400B2 (ja) * | 2019-01-18 | 2022-10-19 | 日産自動車株式会社 | 車体構造 |
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| MX2022008267A (es) | 2020-01-03 | 2022-08-04 | Tesla Inc | Extraccion selectiva de litio a partir de minerales de arcilla. |
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Citations (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2035390A1 (de) | 1969-07-17 | 1971-01-28 | Eastman Kodak Co , Rochester, N Y (VStA) | Formmasse zur Herstellung von Polyester formkorpern |
| DE2248242A1 (de) | 1971-10-01 | 1973-04-12 | Gen Electric | Verstaerkte interkristalline thermoplastische polyester-zusammensetzungen |
| DE2750982A1 (de) | 1977-11-15 | 1979-05-17 | Adlerwerke Kleyer Ag H | Nichtloesbare verbindung von zwei oder mehreren teilen |
| EP0202214A2 (en) | 1985-05-10 | 1986-11-20 | Monsanto Company | Rubber modified nylon composition |
| DE3631540A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Thermoplastische formmassen mit hoher alterungsbestaendigkeit und guter tieftemperaturzaehigkeit |
| DE3631539A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Alterungsbestaendige thermoplastische formmassen mit guter zaehigkeit |
| DE3704655A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| DE3704657A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| EP0370342A2 (de) | 1988-11-25 | 1990-05-30 | Bayer Ag | Leichtbauteil |
| US4937285A (en) | 1987-11-10 | 1990-06-26 | Bayer Aktiengesellschaft | Use of redox graft polymers to improve the petroleum-resistance of thermoplastic, aromatic polycarbonate and/or polyester carbonate moulding compositions |
| DE4236122A1 (de) | 1992-10-27 | 1994-04-28 | Bayer Ag | Flammgeschützte, mineralgefüllte, thermoplastische Formmassen mit hoher Kriechstromfestigkeit |
| EP0785234A1 (en) | 1995-12-29 | 1997-07-23 | Dsm N.V. | Rubber-modified polymer composition |
| EP0679565B1 (fr) | 1994-04-25 | 1998-01-14 | Compagnie Plastic Omnium | Face avant technique de véhicule automobile |
| WO1998011164A1 (en) | 1996-09-10 | 1998-03-19 | E.I. Du Pont De Nemours And Company | Polyamide resin composition |
| WO1998017720A1 (de) | 1996-10-21 | 1998-04-30 | Basf Aktiengesellschaft | Flammgeschützte formmassen |
| WO2001038063A1 (de) | 1999-11-25 | 2001-05-31 | Bayer Aktiengesellschaft | Kunststoffverbundbauteil |
| WO2001040009A1 (de) | 1999-11-29 | 2001-06-07 | Seeber Gmbh | Betätigungshebel zur betätigung mindestens einer vorrichtung, insbesondere in der form eines brems-, kupplungs- oder gaspedals eines kraftfahrzeuges |
| DE10053840A1 (de) | 2000-10-30 | 2002-05-08 | Bayer Ag | Stoßfängersystem für Fahrzeuge |
| EP1223032A2 (de) | 2001-01-11 | 2002-07-17 | Bayer Aktiengesellschaft | Plattenförmiges Leichtbauteil |
| EP1232935A1 (de) | 2001-02-19 | 2002-08-21 | Adam Opel Ag | Fahrzeugkarosserie |
| WO2002068257A1 (en) | 2001-02-28 | 2002-09-06 | E.I. Dupont De Nemours And Company | Integral structures of metal and plastic with fastening means |
| DE10138216A1 (de) | 2001-08-03 | 2003-02-20 | Bayer Ag | Aliphatische Polycarbonathomo- und -copolymere durch DMC-Katalyse |
| US6538024B1 (en) | 1999-02-09 | 2003-03-25 | University Of Virginia Patent Foundation | Felbamate derived compounds |
| DE10147712A1 (de) | 2001-09-27 | 2003-04-17 | Basf Ag | Verfahren zur Herstellung aliphatischer Polycarbonate |
| DE10150061A1 (de) | 2001-10-10 | 2003-05-15 | Hella Behr Fahrzeugsysteme | Metall/Kunststoff-Hybridträger für ein Fahrzeug-Frontmodul |
| DE10163163A1 (de) | 2001-12-20 | 2003-07-03 | Basf Ag | Verfahren zur Herstellung hochfunktioneller, Hyperverzweigter Polyester durch enzymatische Veresterung |
| EP1032526B1 (fr) | 1998-09-30 | 2003-08-13 | Valeo Thermique Moteur | Facade avant composite metal/plastique renforcee surmoulee pour vehicule automobile |
| EP1380493A2 (en) | 2002-07-10 | 2004-01-14 | GP Daikyo Corporation | Front-end panel for a motor vehicle |
| WO2004011315A2 (en) | 2002-07-25 | 2004-02-05 | General Electric Company | Method of attaching plastic to a metal section and part made thereby |
| US6688680B1 (en) | 2002-12-17 | 2004-02-10 | Bayer Polymers Llc | Molded cross vehicle beam |
| EP1211164B1 (en) | 2000-11-29 | 2004-02-18 | Calsonic Kansei Corporation | Radiator support structure of motor vehicle |
| DE10221709A1 (de) | 2002-05-16 | 2004-03-04 | Hella-Behr Fahrzeugsysteme Gmbh | Leichtbauteil für Trägerelemente von Kraftfahrzeugen |
| DE69909629T2 (de) | 1998-06-11 | 2004-04-15 | Rhodia Engineering Plastics S.R.L. | Polyamide mit hoher fliessfähigkeit, verfahren zu ihrer herstellung und zusammensetzungen, die diese copolyamide enthalten |
| US6761187B1 (en) | 2003-04-03 | 2004-07-13 | Bayer Polymers Llc | Tubular assembly having an internal plug |
| WO2004071741A1 (es) | 2003-02-12 | 2004-08-26 | Sintex Beteilingungs, Gmbh. | Procedimiento para la fabricación de una pieza estructural compuesta de un material rígido y un material plástico, y pieza estructural compuesta obtenida |
| EP1294552B1 (de) | 2000-06-21 | 2005-04-06 | ITM International Tools and Moulds GmbH | Verfahren zur herstellung eines hybridteils |
| DE10018186B4 (de) | 2000-04-12 | 2005-07-07 | Acts Gmbh & Co. Kg | Fahrzeugtür und Verfahren zu seiner Herstellung |
| EP1559541A1 (en) | 2002-11-08 | 2005-08-03 | Taisei Plas Co., Ltd. | Composite article of aluminum alloy with resin and method for production thereof |
| EP1958763A1 (en) | 2005-12-08 | 2008-08-20 | Taisei Plas Co., Ltd. | Aluminum alloy-resin composite and method of producing the same |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1340668A3 (de) * | 2002-02-28 | 2003-09-17 | Bayer Ag | Leichtbauteil mit Aussenverrippung |
| DE102006020984A1 (de) * | 2006-05-04 | 2007-11-08 | Lanxess Deutschland Gmbh | Leichtbauteil in Hybridbauweise |
-
2008
- 2008-11-19 DE DE200810058225 patent/DE102008058225A1/de not_active Withdrawn
-
2009
- 2009-11-13 US US12/617,927 patent/US8383242B2/en not_active Expired - Fee Related
- 2009-11-18 KR KR1020090111461A patent/KR20100056402A/ko not_active Withdrawn
- 2009-11-18 JP JP2009263130A patent/JP2010120384A/ja not_active Withdrawn
- 2009-11-19 CN CN200910223652A patent/CN101735603A/zh active Pending
Patent Citations (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2035390A1 (de) | 1969-07-17 | 1971-01-28 | Eastman Kodak Co , Rochester, N Y (VStA) | Formmasse zur Herstellung von Polyester formkorpern |
| DE2248242A1 (de) | 1971-10-01 | 1973-04-12 | Gen Electric | Verstaerkte interkristalline thermoplastische polyester-zusammensetzungen |
| GB1409275A (en) | 1971-10-01 | 1975-10-08 | Gen Electric | Reinforced thermoplastic compositions |
| DE2750982A1 (de) | 1977-11-15 | 1979-05-17 | Adlerwerke Kleyer Ag H | Nichtloesbare verbindung von zwei oder mehreren teilen |
| EP0202214A2 (en) | 1985-05-10 | 1986-11-20 | Monsanto Company | Rubber modified nylon composition |
| US4713415A (en) | 1985-05-10 | 1987-12-15 | Monsanto Company | Rubber modified nylon composition |
| US4806593A (en) | 1986-09-17 | 1989-02-21 | Bayer Aktiengesellschaft | Thermoplastic moulding materials having good resistance to ageing and good low-temperature impact strength |
| DE3631540A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Thermoplastische formmassen mit hoher alterungsbestaendigkeit und guter tieftemperaturzaehigkeit |
| DE3631539A1 (de) | 1986-09-17 | 1988-03-24 | Bayer Ag | Alterungsbestaendige thermoplastische formmassen mit guter zaehigkeit |
| US4812515A (en) | 1986-09-17 | 1989-03-14 | Bayer Aktiengesellschaft | Ageing-resistant thermoplastic moulding materials of good impact strength |
| DE3704655A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| DE3704657A1 (de) | 1987-02-14 | 1988-08-25 | Bayer Ag | Teilchenfoermige mehrphasenpolymerisate |
| US4859740A (en) | 1987-02-14 | 1989-08-22 | Bayer Aktiengesellschaft | Particulate multiphase polymers |
| US4861831A (en) | 1987-02-14 | 1989-08-29 | Bayer Aktiengesellschaft | Particulate multiphase polymers |
| US4937285A (en) | 1987-11-10 | 1990-06-26 | Bayer Aktiengesellschaft | Use of redox graft polymers to improve the petroleum-resistance of thermoplastic, aromatic polycarbonate and/or polyester carbonate moulding compositions |
| EP0370342A2 (de) | 1988-11-25 | 1990-05-30 | Bayer Ag | Leichtbauteil |
| DE4236122A1 (de) | 1992-10-27 | 1994-04-28 | Bayer Ag | Flammgeschützte, mineralgefüllte, thermoplastische Formmassen mit hoher Kriechstromfestigkeit |
| CA2109024A1 (en) | 1992-10-27 | 1994-04-28 | Herbert Magerstedt | Flameproofed, mineral-filled thermoplastic moulding compounds with high tracking resistance |
| EP0679565B1 (fr) | 1994-04-25 | 1998-01-14 | Compagnie Plastic Omnium | Face avant technique de véhicule automobile |
| US5756576A (en) | 1995-12-29 | 1998-05-26 | Dsm N.V. | Rubber-modified polymer composition |
| EP0785234A1 (en) | 1995-12-29 | 1997-07-23 | Dsm N.V. | Rubber-modified polymer composition |
| WO1998011164A1 (en) | 1996-09-10 | 1998-03-19 | E.I. Du Pont De Nemours And Company | Polyamide resin composition |
| WO1998017720A1 (de) | 1996-10-21 | 1998-04-30 | Basf Aktiengesellschaft | Flammgeschützte formmassen |
| DE69909629T2 (de) | 1998-06-11 | 2004-04-15 | Rhodia Engineering Plastics S.R.L. | Polyamide mit hoher fliessfähigkeit, verfahren zu ihrer herstellung und zusammensetzungen, die diese copolyamide enthalten |
| EP1032526B1 (fr) | 1998-09-30 | 2003-08-13 | Valeo Thermique Moteur | Facade avant composite metal/plastique renforcee surmoulee pour vehicule automobile |
| US6538024B1 (en) | 1999-02-09 | 2003-03-25 | University Of Virginia Patent Foundation | Felbamate derived compounds |
| WO2001038063A1 (de) | 1999-11-25 | 2001-05-31 | Bayer Aktiengesellschaft | Kunststoffverbundbauteil |
| WO2001040009A1 (de) | 1999-11-29 | 2001-06-07 | Seeber Gmbh | Betätigungshebel zur betätigung mindestens einer vorrichtung, insbesondere in der form eines brems-, kupplungs- oder gaspedals eines kraftfahrzeuges |
| DE10018186B4 (de) | 2000-04-12 | 2005-07-07 | Acts Gmbh & Co. Kg | Fahrzeugtür und Verfahren zu seiner Herstellung |
| EP1294552B1 (de) | 2000-06-21 | 2005-04-06 | ITM International Tools and Moulds GmbH | Verfahren zur herstellung eines hybridteils |
| DE10053840A1 (de) | 2000-10-30 | 2002-05-08 | Bayer Ag | Stoßfängersystem für Fahrzeuge |
| EP1211164B1 (en) | 2000-11-29 | 2004-02-18 | Calsonic Kansei Corporation | Radiator support structure of motor vehicle |
| EP1223032A2 (de) | 2001-01-11 | 2002-07-17 | Bayer Aktiengesellschaft | Plattenförmiges Leichtbauteil |
| EP1232935A1 (de) | 2001-02-19 | 2002-08-21 | Adam Opel Ag | Fahrzeugkarosserie |
| WO2002068257A1 (en) | 2001-02-28 | 2002-09-06 | E.I. Dupont De Nemours And Company | Integral structures of metal and plastic with fastening means |
| DE10138216A1 (de) | 2001-08-03 | 2003-02-20 | Bayer Ag | Aliphatische Polycarbonathomo- und -copolymere durch DMC-Katalyse |
| DE10147712A1 (de) | 2001-09-27 | 2003-04-17 | Basf Ag | Verfahren zur Herstellung aliphatischer Polycarbonate |
| DE10150061A1 (de) | 2001-10-10 | 2003-05-15 | Hella Behr Fahrzeugsysteme | Metall/Kunststoff-Hybridträger für ein Fahrzeug-Frontmodul |
| DE10163163A1 (de) | 2001-12-20 | 2003-07-03 | Basf Ag | Verfahren zur Herstellung hochfunktioneller, Hyperverzweigter Polyester durch enzymatische Veresterung |
| DE10221709A1 (de) | 2002-05-16 | 2004-03-04 | Hella-Behr Fahrzeugsysteme Gmbh | Leichtbauteil für Trägerelemente von Kraftfahrzeugen |
| EP1380493A2 (en) | 2002-07-10 | 2004-01-14 | GP Daikyo Corporation | Front-end panel for a motor vehicle |
| WO2004011315A2 (en) | 2002-07-25 | 2004-02-05 | General Electric Company | Method of attaching plastic to a metal section and part made thereby |
| EP1559541A1 (en) | 2002-11-08 | 2005-08-03 | Taisei Plas Co., Ltd. | Composite article of aluminum alloy with resin and method for production thereof |
| US6688680B1 (en) | 2002-12-17 | 2004-02-10 | Bayer Polymers Llc | Molded cross vehicle beam |
| WO2004071741A1 (es) | 2003-02-12 | 2004-08-26 | Sintex Beteilingungs, Gmbh. | Procedimiento para la fabricación de una pieza estructural compuesta de un material rígido y un material plástico, y pieza estructural compuesta obtenida |
| US6761187B1 (en) | 2003-04-03 | 2004-07-13 | Bayer Polymers Llc | Tubular assembly having an internal plug |
| EP1958763A1 (en) | 2005-12-08 | 2008-08-20 | Taisei Plas Co., Ltd. | Aluminum alloy-resin composite and method of producing the same |
Non-Patent Citations (17)
| Title |
|---|
| "Degree of Branching" siehe H. Frey et al., Acta Polym. 1997, 48, 30 |
| "Ullmann's Encyclopedia of Industrial Chemistry", 6th Edition, 2000 Electronic Release, Verlag Wiley-VCH |
| A. Sunder et al., Chem. Eur. J. 2000, 6, No. 1, 1-8 |
| DIN 53019 |
| DIN 53240 |
| DIN 53240, Teil 2 |
| DIN 53765 |
| G�chter, M�ller, Kunststoff-Additive, 3. Ausgabe, Hanser-Verlag, M�nchen, Wien, 1989 |
| H. Frey et al. Acta Polym. 1997, 48, 30 |
| Joining Plastics, 3/08 Seiten 210-217 |
| Kunststoff-Taschenbuch (Hrsg. Saechtling), Auflage 1989 |
| Kurt Faber, "Biotransformations in Organic Chemistry", 3. Auflage 1997, Springer Verlag, Kapitel 3.2 "Immobilization" Seite 345-356 |
| P. J. Flory, J. Am. Chem. Soc. 1952, 74, 2718 |
| P. J. Flory, J. Am. Chem. Soc. 1952, 74, 2718 und H. Frey et al., Chem. Eur. J. 2000, 6, No. 14, 2499 |
| Plastics Additives Handbook, 5th Edition, Hanser-Verlag, M�nchen, 2001 |
| Standard PMMA) auf |
| Ullmann, Enzyklop�die der Technischen Chemie, Bd. 19 (1980), S. 280 ff |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2010120384A (ja) | 2010-06-03 |
| US8383242B2 (en) | 2013-02-26 |
| KR20100056402A (ko) | 2010-05-27 |
| US20100173126A1 (en) | 2010-07-08 |
| CN101735603A (zh) | 2010-06-16 |
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