DE112006000348T5 - Stabilisierung von natürlichen Komposit- bzw. Verbundwerkstoffen - Google Patents
Stabilisierung von natürlichen Komposit- bzw. Verbundwerkstoffen Download PDFInfo
- Publication number
- DE112006000348T5 DE112006000348T5 DE112006000348T DE112006000348T DE112006000348T5 DE 112006000348 T5 DE112006000348 T5 DE 112006000348T5 DE 112006000348 T DE112006000348 T DE 112006000348T DE 112006000348 T DE112006000348 T DE 112006000348T DE 112006000348 T5 DE112006000348 T5 DE 112006000348T5
- Authority
- DE
- Germany
- Prior art keywords
- carbon atoms
- tetramethyl
- alkyl
- hydroxy
- hydroxypiperidinium
- 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.)
- Withdrawn
Links
- 239000002131 composite material Substances 0.000 title claims abstract description 74
- 230000006641 stabilisation Effects 0.000 title description 4
- 238000011105 stabilization Methods 0.000 title description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 284
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 184
- -1 cyanohydrin Chemical class 0.000 claims abstract description 156
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 121
- 239000001257 hydrogen Chemical group 0.000 claims abstract description 117
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 86
- 239000002023 wood Substances 0.000 claims abstract description 81
- 239000000203 mixture Substances 0.000 claims abstract description 66
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 53
- 150000001412 amines Chemical class 0.000 claims abstract description 49
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 45
- 239000000945 filler Substances 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 229920002678 cellulose Polymers 0.000 claims abstract description 22
- 239000001913 cellulose Substances 0.000 claims abstract description 22
- 150000002148 esters Chemical class 0.000 claims abstract description 19
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 14
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims abstract description 13
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims abstract description 12
- 230000015556 catabolic process Effects 0.000 claims abstract description 10
- 238000006731 degradation reaction Methods 0.000 claims abstract description 10
- 150000001768 cations Chemical class 0.000 claims abstract description 9
- 125000005647 linker group Chemical group 0.000 claims abstract description 9
- 150000001408 amides Chemical class 0.000 claims abstract description 8
- 125000004043 oxo group Chemical group O=* 0.000 claims abstract description 6
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000003960 organic solvent Substances 0.000 claims abstract description 5
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 4
- 150000007524 organic acids Chemical class 0.000 claims abstract description 4
- 229920001577 copolymer Chemical compound 0.000 claims description 88
- 150000002431 hydrogen Chemical class 0.000 claims description 59
- 125000002947 alkylene group Chemical group 0.000 claims description 55
- 229920000642 polymer Polymers 0.000 claims description 54
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 53
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 41
- QPCDCPDFJACHGM-UHFFFAOYSA-K pentetate(3-) Chemical compound OC(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O QPCDCPDFJACHGM-UHFFFAOYSA-K 0.000 claims description 36
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 24
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 24
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- CSGAUKGQUCHWDP-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1O CSGAUKGQUCHWDP-UHFFFAOYSA-N 0.000 claims description 19
- 239000005977 Ethylene Substances 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 17
- JWUXJYZVKZKLTJ-UHFFFAOYSA-N Triacetonamine Chemical compound CC1(C)CC(=O)CC(C)(C)N1 JWUXJYZVKZKLTJ-UHFFFAOYSA-N 0.000 claims description 16
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 16
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
- 229940071106 ethylenediaminetetraacetate Drugs 0.000 claims description 13
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 235000013312 flour Nutrition 0.000 claims description 12
- NWHNXXMYEICZAT-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-ol Chemical compound CN1C(C)(C)CC(O)CC1(C)C NWHNXXMYEICZAT-UHFFFAOYSA-N 0.000 claims description 11
- YZOYCEJFGBMHNJ-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylate;1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol Chemical compound C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YZOYCEJFGBMHNJ-UHFFFAOYSA-N 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 11
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 11
- 238000001035 drying Methods 0.000 claims description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 11
- YYTYIUAYFBFKHX-UHFFFAOYSA-N n-(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl)acetamide Chemical compound CC(=O)NC1CC(C)(C)N(O)C(C)(C)C1 YYTYIUAYFBFKHX-UHFFFAOYSA-N 0.000 claims description 11
- KKMOKJFLZOIBFP-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylate;2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KKMOKJFLZOIBFP-UHFFFAOYSA-N 0.000 claims description 10
- TXXNVPVRPSACBM-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O TXXNVPVRPSACBM-UHFFFAOYSA-N 0.000 claims description 10
- 239000007983 Tris buffer Substances 0.000 claims description 10
- 125000004450 alkenylene group Chemical group 0.000 claims description 10
- 150000007942 carboxylates Chemical class 0.000 claims description 10
- 239000003381 stabilizer Substances 0.000 claims description 10
- CRGBPDJWOLULDY-UHFFFAOYSA-N (1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) acetate Chemical compound CC(=O)OC1CC(C)(C)N(O)C(C)(C)C1 CRGBPDJWOLULDY-UHFFFAOYSA-N 0.000 claims description 9
- 229920002522 Wood fibre Polymers 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- WFIYJMCNWNWOCL-UHFFFAOYSA-N n-(1,2,2,6,6-pentamethylpiperidin-4-yl)acetamide Chemical compound CN1C(C)(C)CC(NC(C)=O)CC1(C)C WFIYJMCNWNWOCL-UHFFFAOYSA-N 0.000 claims description 9
- XULIXFLCVXWHRF-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidine Chemical compound CN1C(C)(C)CCCC1(C)C XULIXFLCVXWHRF-UHFFFAOYSA-N 0.000 claims description 8
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 8
- 150000001450 anions Chemical class 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 8
- HVXYQAREJSKQNE-UHFFFAOYSA-N n-(2,2,6,6-tetramethylpiperidin-4-yl)acetamide Chemical compound CC(=O)NC1CC(C)(C)NC(C)(C)C1 HVXYQAREJSKQNE-UHFFFAOYSA-N 0.000 claims description 8
- 229910052727 yttrium Inorganic materials 0.000 claims description 8
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 230000000737 periodic effect Effects 0.000 claims description 7
- 239000002025 wood fiber Substances 0.000 claims description 7
- OEAJJNMBFKSVHF-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-1-ium;chloride Chemical compound Cl.CN1C(C)(C)CCCC1(C)C OEAJJNMBFKSVHF-UHFFFAOYSA-N 0.000 claims description 6
- VPCQZJQTSDJOJD-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium;chloride Chemical compound [Cl-].CC1(C)CCCC(C)(C)[NH+]1O VPCQZJQTSDJOJD-UHFFFAOYSA-N 0.000 claims description 6
- VDVUCLWJZJHFAV-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)N1 VDVUCLWJZJHFAV-UHFFFAOYSA-N 0.000 claims description 6
- QQKSUFBBIKGEOK-UHFFFAOYSA-N 2-(carboxymethyl)-2-hydroxybutanedioate;1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol Chemical compound C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.OC(=O)CC(O)(C([O-])=O)CC([O-])=O QQKSUFBBIKGEOK-UHFFFAOYSA-N 0.000 claims description 6
- ZSBHIJSEKKTCLM-UHFFFAOYSA-N 2-(carboxymethyl)-2-hydroxybutanedioate;2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.OC(=O)CC(O)(C([O-])=O)CC([O-])=O ZSBHIJSEKKTCLM-UHFFFAOYSA-N 0.000 claims description 6
- YWBXOXPKPRNECI-UHFFFAOYSA-N 2-hydroxypropane-1,2,3-tricarboxylic acid;1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.OC(=O)CC(O)(C([O-])=O)CC([O-])=O YWBXOXPKPRNECI-UHFFFAOYSA-N 0.000 claims description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 6
- 125000000732 arylene group Chemical group 0.000 claims description 6
- 125000001589 carboacyl group Chemical group 0.000 claims description 6
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims description 6
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 6
- 229910021645 metal ion Inorganic materials 0.000 claims description 6
- 125000001624 naphthyl group Chemical group 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 239000003921 oil Substances 0.000 claims description 6
- 239000002245 particle Substances 0.000 claims description 6
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 6
- 229910052698 phosphorus Inorganic materials 0.000 claims description 6
- 229940124543 ultraviolet light absorber Drugs 0.000 claims description 6
- 125000006839 xylylene group Chemical group 0.000 claims description 6
- GHJUORCGZFHNKG-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-4-one Chemical compound CN1C(C)(C)CC(=O)CC1(C)C GHJUORCGZFHNKG-UHFFFAOYSA-N 0.000 claims description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
- 238000001125 extrusion Methods 0.000 claims description 5
- 239000003063 flame retardant Substances 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 239000000155 melt Substances 0.000 claims description 5
- 238000000465 moulding Methods 0.000 claims description 5
- 230000008569 process Effects 0.000 claims description 5
- 229910052725 zinc Inorganic materials 0.000 claims description 5
- KKZZSTCINUMTGD-UHFFFAOYSA-N 1,2,2,3-tetramethylpiperidin-4-ol Chemical compound CC1C(O)CCN(C)C1(C)C KKZZSTCINUMTGD-UHFFFAOYSA-N 0.000 claims description 4
- DEDVHXDPTGULHZ-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol;acetate Chemical compound CC([O-])=O.C[NH+]1C(C)(C)CC(O)CC1(C)C DEDVHXDPTGULHZ-UHFFFAOYSA-N 0.000 claims description 4
- VOFUCRVRAJDIIO-UHFFFAOYSA-N 1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol;chloride Chemical compound Cl.CN1C(C)(C)CC(O)CC1(C)C VOFUCRVRAJDIIO-UHFFFAOYSA-N 0.000 claims description 4
- QDNPLNOHUNPYHZ-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethyl-4-propoxypiperidine Chemical compound CCCOC1CC(C)(C)N(O)C(C)(C)C1 QDNPLNOHUNPYHZ-UHFFFAOYSA-N 0.000 claims description 4
- QCJDXHSSMDQRBO-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium-4-ol;chloride Chemical compound [Cl-].CC1(C)CC(O)CC(C)(C)[NH+]1O QCJDXHSSMDQRBO-UHFFFAOYSA-N 0.000 claims description 4
- KMEUSKGEUADGET-UHFFFAOYSA-N 1-hydroxy-2,2,6,6-tetramethylpiperidin-4-one Chemical compound CC1(C)CC(=O)CC(C)(C)N1O KMEUSKGEUADGET-UHFFFAOYSA-N 0.000 claims description 4
- KRNWYBIEWUXCOB-UHFFFAOYSA-N 1-hydroxy-4-methoxy-2,2,6,6-tetramethylpiperidine Chemical compound COC1CC(C)(C)N(O)C(C)(C)C1 KRNWYBIEWUXCOB-UHFFFAOYSA-N 0.000 claims description 4
- VUZNLSBZRVZGIK-UHFFFAOYSA-N 2,2,6,6-Tetramethyl-1-piperidinol Chemical compound CC1(C)CCCC(C)(C)N1O VUZNLSBZRVZGIK-UHFFFAOYSA-N 0.000 claims description 4
- NHEMTMCGXCQOBI-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidin-1-ium-4-ol;chloride Chemical compound Cl.CC1(C)CC(O)CC(C)(C)N1 NHEMTMCGXCQOBI-UHFFFAOYSA-N 0.000 claims description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- SXSOYHNXNFJNNU-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate 1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol Chemical compound C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.C[NH+]1C(C)(C)CC(O)CC1(C)C.[O-]C(=O)CN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O SXSOYHNXNFJNNU-UHFFFAOYSA-N 0.000 claims description 4
- ISNDZKFXDICEFL-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate 2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.CC1(C)CC(O)CC(C)(C)[NH2+]1.[O-]C(=O)CN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O ISNDZKFXDICEFL-UHFFFAOYSA-N 0.000 claims description 4
- VXTQQZJIEZVZFT-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate N-(2,2,6,6-tetramethylpiperidin-1-ium-4-yl)acetamide Chemical compound CC(=O)NC1CC(C)(C)[NH2+]C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH2+]C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH2+]C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH2+]C(C)(C)C1.[O-]C(=O)CN(CCN(CC([O-])=O)CC([O-])=O)CC([O-])=O VXTQQZJIEZVZFT-UHFFFAOYSA-N 0.000 claims description 4
- IMNZCNLFZBWMDI-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;1-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.CC1(C)CC(O)CC(C)(C)[NH+]1O.[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O IMNZCNLFZBWMDI-UHFFFAOYSA-N 0.000 claims description 4
- CAZAXTALZNYAGA-UHFFFAOYSA-N 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;n-(1-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium-4-yl)acetamide Chemical compound CC(=O)NC1CC(C)(C)[NH+](O)C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH+](O)C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH+](O)C(C)(C)C1.CC(=O)NC1CC(C)(C)[NH+](O)C(C)(C)C1.[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O CAZAXTALZNYAGA-UHFFFAOYSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- 229910052770 Uranium Inorganic materials 0.000 claims description 4
- LUTRAMFAYXFIQK-UHFFFAOYSA-N acetic acid;1-hydroxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC([O-])=O.CC1(C)CC(O)CC(C)(C)[NH+]1O LUTRAMFAYXFIQK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 235000010233 benzoic acid Nutrition 0.000 claims description 4
- SXPLGYBFGPYAHS-UHFFFAOYSA-N bis(1-hydroxy-2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)N(O)C(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)N(O)C(C)(C)C1 SXPLGYBFGPYAHS-UHFFFAOYSA-N 0.000 claims description 4
- 239000011111 cardboard Substances 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 150000002334 glycols Chemical class 0.000 claims description 4
- UOWRZBNGZFDQHW-UHFFFAOYSA-N hydrogen sulfate;1,2,2,6,6-pentamethylpiperidin-1-ium-4-ol Chemical compound OS([O-])(=O)=O.C[NH+]1C(C)(C)CC(O)CC1(C)C UOWRZBNGZFDQHW-UHFFFAOYSA-N 0.000 claims description 4
- REZIEVJVJYHZKK-UHFFFAOYSA-N hydrogen sulfate;1-hydroxy-2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound OS([O-])(=O)=O.CC1(C)CC(O)CC(C)(C)[NH+]1O REZIEVJVJYHZKK-UHFFFAOYSA-N 0.000 claims description 4
- HZKWVGOFKYJSGM-UHFFFAOYSA-N hydrogen sulfate;2,2,6,6-tetramethylpiperidin-1-ium-4-ol Chemical compound OS([O-])(=O)=O.CC1(C)CC(O)CC(C)(C)[NH2+]1 HZKWVGOFKYJSGM-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 4
- GCZDACZURJFILX-UHFFFAOYSA-N hydron;2,2,6,6-tetramethylpiperidine;chloride Chemical compound Cl.CC1(C)CCCC(C)(C)N1 GCZDACZURJFILX-UHFFFAOYSA-N 0.000 claims description 4
- 238000010128 melt processing Methods 0.000 claims description 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 4
- 229910052759 nickel Inorganic materials 0.000 claims description 4
- 239000000123 paper Substances 0.000 claims description 4
- 150000002989 phenols Chemical class 0.000 claims description 4
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 4
- XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 claims description 4
- 229910052721 tungsten Inorganic materials 0.000 claims description 4
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- RNVAPPWJCZTWQL-UHFFFAOYSA-N octadecyl 3,5-ditert-butyl-4-hydroxybenzoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 RNVAPPWJCZTWQL-UHFFFAOYSA-N 0.000 description 1
- 125000005474 octanoate group Chemical group 0.000 description 1
- XQAABEDPVQWFPN-UHFFFAOYSA-N octyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=CC=CC3=N2)=C1O XQAABEDPVQWFPN-UHFFFAOYSA-N 0.000 description 1
- DMFXLIFZVRXRRR-UHFFFAOYSA-N octyl 3-[3-tert-butyl-5-(5-chlorobenzotriazol-2-yl)-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OCCCCCCCC)=CC(N2N=C3C=C(Cl)C=CC3=N2)=C1O DMFXLIFZVRXRRR-UHFFFAOYSA-N 0.000 description 1
- NTTIENRNNNJCHQ-UHFFFAOYSA-N octyl n-(3,5-ditert-butyl-4-hydroxyphenyl)carbamate Chemical compound CCCCCCCCOC(=O)NC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NTTIENRNNNJCHQ-UHFFFAOYSA-N 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- ZPNJBTBYIHBSIG-UHFFFAOYSA-N phenyl-(2,2,6,6-tetramethylpiperidin-4-yl)methanone Chemical compound C1C(C)(C)NC(C)(C)CC1C(=O)C1=CC=CC=C1 ZPNJBTBYIHBSIG-UHFFFAOYSA-N 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 230000008832 photodamage Effects 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920001627 poly(4-methyl styrene) Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920003251 poly(α-methylstyrene) Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229940068886 polyethylene glycol 300 Drugs 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000010817 post-consumer waste Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical class C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000011122 softwood Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229920000638 styrene acrylonitrile Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical compound NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 description 1
- 150000000000 tetracarboxylic acids Chemical class 0.000 description 1
- NZNAAUDJKMURFU-UHFFFAOYSA-N tetrakis(2,2,6,6-tetramethylpiperidin-4-yl) butane-1,2,3,4-tetracarboxylate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CC(C(=O)OC1CC(C)(C)NC(C)(C)C1)C(C(=O)OC1CC(C)(C)NC(C)(C)C1)CC(=O)OC1CC(C)(C)NC(C)(C)C1 NZNAAUDJKMURFU-UHFFFAOYSA-N 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 150000003627 tricarboxylic acid derivatives Chemical class 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
- 150000004684 trihydrates Chemical class 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 description 1
- 229920006337 unsaturated polyester resin Polymers 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08H—DERIVATIVES OF NATURAL MACROMOLECULAR COMPOUNDS
- C08H8/00—Macromolecular compounds derived from lignocellulosic materials
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L97/00—Compositions of lignin-containing materials
- C08L97/02—Lignocellulosic material, e.g. wood, straw or bagasse
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/022—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/07—Flat, e.g. panels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/06—Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
- B29K2105/16—Fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/04—Ingredients treated with organic substances
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Wood Science & Technology (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65317005P | 2005-02-15 | 2005-02-15 | |
| US60/653,170 | 2005-02-15 | ||
| PCT/EP2006/050673 WO2006087269A1 (en) | 2005-02-15 | 2006-02-06 | Stabilization of natural composites |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE112006000348T5 true DE112006000348T5 (de) | 2007-12-27 |
Family
ID=36379135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE112006000348T Withdrawn DE112006000348T5 (de) | 2005-02-15 | 2006-02-06 | Stabilisierung von natürlichen Komposit- bzw. Verbundwerkstoffen |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US7862746B2 (https=) |
| JP (1) | JP4963472B2 (https=) |
| DE (1) | DE112006000348T5 (https=) |
| WO (1) | WO2006087269A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102018103443A1 (de) * | 2018-02-15 | 2019-08-22 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Herstellung eines Verbundteils |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1456296A1 (de) * | 2001-12-20 | 2004-09-15 | AMI Agrolinz Melamine International GmbH | Additiv zur inhibierung von photolytischen abbaureaktionen in aminoplasten |
| US7875655B2 (en) | 2006-01-20 | 2011-01-25 | Material Innovations, Llc | Carpet waste composite |
| EP2114648B1 (en) * | 2006-11-22 | 2014-09-03 | Material Innovations, LLC | Wood-plastic composites using recycled carpet waste and methods of manufacturing |
| DE102007028374B4 (de) * | 2007-06-11 | 2009-04-23 | Ava - Anhaltinische Verfahrens- Und Anlagentechnik Gmbh | Verfahren zur Herstellung eines Holz-Kunststoff-Verbundwerkstoffes |
| CN101688100B (zh) * | 2007-07-06 | 2012-04-18 | 汉高公司 | 丙烯酸系粘合剂 |
| US20090036566A1 (en) * | 2007-07-30 | 2009-02-05 | City University Of Hong Kong | Biodegradable composite, product made therefrom, and method of manufacture thereof |
| WO2009084566A1 (ja) * | 2007-12-28 | 2009-07-09 | Nippon Paper Industries Co., Ltd. | セルロースナノファイバーの製造方法、セルロースの酸化触媒及びセルロースの酸化方法 |
| US20090321981A1 (en) * | 2008-01-15 | 2009-12-31 | RheTech, Inc. | Cellulosic inclusion thermoplastic composition and molding thereof |
| JP5361217B2 (ja) * | 2008-02-29 | 2013-12-04 | 株式会社Adeka | 耐候性の改善された木質系合成樹脂組成物およびその成形体 |
| KR20110123240A (ko) | 2008-12-19 | 2011-11-14 | 파이버 콤포지트 엘엘씨. | 이오노머 캡스톡을 이용한 목재-플라스틱 복합물 그리고 그 제조 방법 |
| US8901209B2 (en) | 2010-04-21 | 2014-12-02 | Sabic Global Technologies B.V. | Wood-plastic composite with improved thermal and weathering resistance and method of making the same |
| CN102233603B (zh) * | 2010-05-07 | 2013-07-03 | 潘金瓶 | 轻质户外重组竹景观材料的制造方法 |
| FR2966372B1 (fr) * | 2010-10-26 | 2013-08-23 | Berkem Sa | Composition pour le traitement du bois |
| BRPI1101225A2 (pt) * | 2011-03-04 | 2013-06-04 | Madeplast Ind E Com De Madeira Plastica Ltda Me | composiÇço de material compàsito termoplÁstico, produto compàsito termoplÁstico e mÉtodo para sua produÇço |
| US8747709B2 (en) | 2012-05-03 | 2014-06-10 | Empire Technology Development Llc | Phosphonate-substituted lignin as a flame retardant |
| JP6486429B2 (ja) * | 2017-08-29 | 2019-03-20 | 旭化成株式会社 | セルロース充填樹脂組成物の製造方法 |
| JP6979933B2 (ja) * | 2017-08-29 | 2021-12-15 | 旭化成株式会社 | セルロース充填樹脂組成物の製造方法 |
| CN109337353B (zh) * | 2018-07-23 | 2020-12-11 | 汕头市华莎驰家具家饰有限公司 | 一种表面改性纤维增强聚氨酯复合材料及其制备方法 |
| CN110076869A (zh) * | 2019-06-13 | 2019-08-02 | 毛克升 | 一种竹材防霉防蛀处理剂及其制备方法与施工工艺 |
| KR102072501B1 (ko) * | 2019-07-03 | 2020-02-03 | 주식회사 하성 | 열안정성이 우수한 이중압출 합성목재 및 그 제조방법 |
| CN110815487A (zh) * | 2019-08-02 | 2020-02-21 | 浙江焱木科技有限公司 | 一种木质防火压力板及其制造方法 |
| KR102099148B1 (ko) * | 2019-10-22 | 2020-04-09 | (주)우드린 | 난연성 합성목재 제조방법 |
| CN111138343A (zh) * | 2019-12-26 | 2020-05-12 | 宿迁联盛科技股份有限公司 | 三(2,2,6,6-四甲基哌啶醇)柠檬酸盐及其制备方法 |
| CA3188593A1 (en) * | 2020-07-14 | 2022-01-20 | Ut-Battelle, Llc | Surface-modified and dried microfibrillated cellulose reinforced thermoplastic biocomposites |
| US11572646B2 (en) | 2020-11-18 | 2023-02-07 | Material Innovations Llc | Composite building materials and methods of manufacture |
| US12172421B2 (en) | 2020-11-18 | 2024-12-24 | Rise Building Products Llc | Composite building materials and methods of manufacture |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6180257B1 (en) * | 1996-10-29 | 2001-01-30 | Crane Plastics Company Limited Partnership | Compression molding of synthetic wood material |
| RU2223985C2 (ru) * | 1997-07-23 | 2004-02-20 | Циба Спешиалти Кемикалз Холдинг Инк. | Ингибирование пожелтения целлюлозы и бумаги с использованием нитроксидов и других совместно вводимых добавок |
| TWI224995B (en) * | 1998-03-19 | 2004-12-11 | Ciba Sc Holding Ag | Stabilization of wood substrates |
| US6164034A (en) * | 1998-08-31 | 2000-12-26 | Poly Proximates, Inc. | Fiber-reinforced molded plastic roofing unit and method of making the same |
| JP2001064526A (ja) * | 1999-08-31 | 2001-03-13 | Kotobuki Sangyo Kk | 竹粉と熱可塑性樹脂の抗菌性を有する混合材料及びその製造方法 |
| TW514581B (en) * | 1999-09-02 | 2002-12-21 | Ciba Sc Holding Ag | A method of protecting wood against light-induced degradation by treatment with an impregnation which penetrates the surface of the wood |
| JP2002137333A (ja) * | 2000-11-06 | 2002-05-14 | Sekisui Chem Co Ltd | 木質含有部材 |
| US20030121630A1 (en) * | 2000-04-19 | 2003-07-03 | Zhirun Yuan | Inhibition of yellowing in papers |
| AUPQ909800A0 (en) * | 2000-07-31 | 2000-08-24 | Commonwealth Scientific And Industrial Research Organisation | Cellulose reinforced composite compositions |
| WO2002025007A2 (en) * | 2000-09-18 | 2002-03-28 | Pulp And Paper Research Institute Of Canada | Light-stable lignocellulosic materials and their production_____ |
| DE10127749A1 (de) * | 2001-06-07 | 2002-12-12 | Bayer Ag | Verbund enthaltend ABS |
| KR100414765B1 (ko) * | 2001-06-15 | 2004-01-13 | 한국과학기술연구원 | 세라믹 칩 안테나 |
| AT411452B (de) * | 2001-12-20 | 2004-01-26 | Agrolinz Melamin Gmbh | Uv-resistenter, thermohärtbarer aminoplastverbund, dessen herstellung und verwendung |
| US20040076847A1 (en) * | 2002-10-17 | 2004-04-22 | Saunders Howard E. | Colored wood/polymer composites |
| JP4165190B2 (ja) * | 2002-11-08 | 2008-10-15 | 凸版印刷株式会社 | 化粧材 |
| CA2522969A1 (en) * | 2003-04-23 | 2004-11-04 | Ciba Specialty Chemicals Holding Inc. | Natural products composites |
-
2006
- 2006-02-06 DE DE112006000348T patent/DE112006000348T5/de not_active Withdrawn
- 2006-02-06 WO PCT/EP2006/050673 patent/WO2006087269A1/en not_active Ceased
- 2006-02-06 JP JP2007555572A patent/JP4963472B2/ja not_active Expired - Fee Related
- 2006-02-13 US US11/352,873 patent/US7862746B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102018103443A1 (de) * | 2018-02-15 | 2019-08-22 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Herstellung eines Verbundteils |
Also Published As
| Publication number | Publication date |
|---|---|
| US20060183821A1 (en) | 2006-08-17 |
| JP2008531324A (ja) | 2008-08-14 |
| JP4963472B2 (ja) | 2012-06-27 |
| US7862746B2 (en) | 2011-01-04 |
| WO2006087269A1 (en) | 2006-08-24 |
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