NL1004094C2 - Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. - Google Patents
Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. Download PDFInfo
- Publication number
- NL1004094C2 NL1004094C2 NL1004094A NL1004094A NL1004094C2 NL 1004094 C2 NL1004094 C2 NL 1004094C2 NL 1004094 A NL1004094 A NL 1004094A NL 1004094 A NL1004094 A NL 1004094A NL 1004094 C2 NL1004094 C2 NL 1004094C2
- Authority
- NL
- Netherlands
- Prior art keywords
- dendrimer
- plastic
- end groups
- molded part
- fibers
- Prior art date
Links
- 229920003023 plastic Polymers 0.000 title claims abstract description 37
- 239000004033 plastic Substances 0.000 title claims abstract description 37
- 238000000034 method Methods 0.000 title claims abstract description 34
- 239000013543 active substance Substances 0.000 title claims abstract description 22
- 239000000412 dendrimer Substances 0.000 claims abstract description 67
- 229920000736 dendritic polymer Polymers 0.000 claims abstract description 67
- 239000000835 fiber Substances 0.000 claims description 48
- -1 polypropylene Polymers 0.000 claims description 27
- 150000001875 compounds Chemical class 0.000 claims description 20
- 239000004743 Polypropylene Substances 0.000 claims description 19
- 229920001155 polypropylene Polymers 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 18
- 229920000642 polymer Polymers 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 230000007547 defect Effects 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 238000011835 investigation Methods 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
- 239000000975 dye Substances 0.000 description 25
- 235000021355 Stearic acid Nutrition 0.000 description 10
- 238000004040 coloring Methods 0.000 description 10
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 10
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 10
- 239000008117 stearic acid Substances 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 8
- 229930195729 fatty acid Natural products 0.000 description 8
- 239000000194 fatty acid Substances 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 229920000333 poly(propyleneimine) Polymers 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- 230000000007 visual effect Effects 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920006380 polyphenylene oxide Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XEMMSXIXTJAXOT-UHFFFAOYSA-N 6-amino-5-[[2-[cyclohexyl(methyl)sulfamoyl]phenyl]diazenyl]-4-hydroxynaphthalene-2-sulfonic acid Chemical compound CN(C1CCCCC1)S(=O)(=O)C1=C(C=CC=C1)N=NC1=C(N)C=CC2=CC(=CC(O)=C12)S(O)(=O)=O XEMMSXIXTJAXOT-UHFFFAOYSA-N 0.000 description 2
- 229920002943 EPDM rubber Polymers 0.000 description 2
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical class [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000012679 convergent method Methods 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 238000012678 divergent method Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 239000003063 flame retardant Substances 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Chemical class 0.000 description 2
- 229920000962 poly(amidoamine) Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920001281 polyalkylene Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- GFLXBRUGMACJLQ-UHFFFAOYSA-N 1-isocyanatohexadecane Chemical compound CCCCCCCCCCCCCCCCN=C=O GFLXBRUGMACJLQ-UHFFFAOYSA-N 0.000 description 1
- DWYWPBYWDAZKNX-UHFFFAOYSA-N 2,5-dichloro-4-[3-methyl-5-oxo-4-[(4-sulfophenyl)diazenyl]-4h-pyrazol-1-yl]benzenesulfonic acid Chemical compound CC1=NN(C=2C(=CC(=C(Cl)C=2)S(O)(=O)=O)Cl)C(=O)C1N=NC1=CC=C(S(O)(=O)=O)C=C1 DWYWPBYWDAZKNX-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- XTRPJEPJFXGYCI-UHFFFAOYSA-N 3-chloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)CCl XTRPJEPJFXGYCI-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229920002614 Polyether block amide Polymers 0.000 description 1
- 229920002873 Polyethylenimine Polymers 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 229920002396 Polyurea Polymers 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000006750 UV protection Effects 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 239000004234 Yellow 2G Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000008430 aromatic amides Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229920005605 branched copolymer Polymers 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920005556 chlorobutyl Polymers 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- ARBOVOVUTSQWSS-UHFFFAOYSA-N hexadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCC(Cl)=O ARBOVOVUTSQWSS-UHFFFAOYSA-N 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- RSAZYXZUJROYKR-UHFFFAOYSA-N indophenol Chemical compound C1=CC(O)=CC=C1N=C1C=CC(=O)C=C1 RSAZYXZUJROYKR-UHFFFAOYSA-N 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001643 poly(ether ketone) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000412 polyarylene Polymers 0.000 description 1
- 229920002480 polybenzimidazole Polymers 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920006295 polythiol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003254 radicals Chemical group 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229940037312 stearamide Drugs 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 235000019235 yellow 2G Nutrition 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
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
- C08G83/003—Dendrimers
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
- C08L101/005—Dendritic macromolecules
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/02—Polyamines
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/44—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds
- D01F6/46—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds as major constituent with other polymers or low-molecular-weight compounds of polyolefins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/79—Polyolefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/12—Applications used for fibers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L87/00—Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Textile Engineering (AREA)
- General Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Artificial Filaments (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Coloring (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1004094A NL1004094C2 (nl) | 1996-09-23 | 1996-09-23 | Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. |
| DE69709663T DE69709663T2 (de) | 1996-09-23 | 1997-09-22 | Verfahren zum einarbeiten eines wirkstoffes in ein kunstoffbauteil |
| CA002266586A CA2266586A1 (en) | 1996-09-23 | 1997-09-22 | Process for incorporating an active substance in a moulded plastic part |
| EA199900323A EA199900323A1 (ru) | 1996-09-23 | 1997-09-22 | Способ введения активного вещества в отформованную пластмассовую деталь |
| CN97199797A CN1238018A (zh) | 1996-09-23 | 1997-09-22 | 将活性物质掺入模塑塑料制件的方法 |
| IL12908797A IL129087A0 (en) | 1996-09-23 | 1997-09-22 | Process for incorporating an active substance in a moulded plastic part |
| SK390-99A SK39099A3 (en) | 1996-09-23 | 1997-09-22 | Process for incorporating an active substance in a moulded plastic part |
| PL97332374A PL332374A1 (en) | 1996-09-23 | 1997-09-22 | Method of introducing an active substance into a portion of plastic moulding |
| CZ991031A CZ103199A3 (cs) | 1996-09-23 | 1997-09-22 | Způsob začlenění aktivní látky do tvarovaného plastového dílu |
| JP10514540A JP2001502015A (ja) | 1996-09-23 | 1997-09-22 | 成形プラスチック部品に作用物質を含有させる方法 |
| AU42252/97A AU4225297A (en) | 1996-09-23 | 1997-09-22 | Process for incorporating an active substance in a moulded plastic part |
| BR9711533A BR9711533A (pt) | 1996-09-23 | 1997-09-22 | Processo para a incorpora-Æo de uma subst ncia ativa em uma pe-a de pl stico moldada |
| EP97940486A EP0927275B1 (de) | 1996-09-23 | 1997-09-22 | Verfahren zum einarbeiten eines wirkstoffes in ein kunstoffbauteil |
| TR1999/00643T TR199900643T2 (xx) | 1996-09-23 | 1997-09-22 | Bir etken maddeyi kal�planm�� bir plastik par�aya dahil etmek i�in i�lem. |
| PCT/NL1997/000527 WO1998012376A1 (en) | 1996-09-23 | 1997-09-22 | Process for incorporating an active substance in a moulded plastic part |
| HU9903833A HUP9903833A2 (hu) | 1996-09-23 | 1997-09-22 | Eljárás egy aktív anyag bedolgozására formázott műanyag tárgyba |
| AT97940486T ATE212083T1 (de) | 1996-09-23 | 1997-09-22 | Verfahren zum einarbeiten eines wirkstoffes in ein kunstoffbauteil |
| NO991379A NO991379L (no) | 1996-09-23 | 1999-03-22 | FremgangsmÕte ved innarbeidelse av en aktiv substans i en st°pt plastdel |
| US09/275,140 US6232378B1 (en) | 1996-09-23 | 1999-03-23 | Process for incorporating an active substance in a moulded plastic part |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL1004094A NL1004094C2 (nl) | 1996-09-23 | 1996-09-23 | Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. |
| NL1004094 | 1996-09-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL1004094C2 true NL1004094C2 (nl) | 1998-03-24 |
Family
ID=19763552
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL1004094A NL1004094C2 (nl) | 1996-09-23 | 1996-09-23 | Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6232378B1 (de) |
| EP (1) | EP0927275B1 (de) |
| JP (1) | JP2001502015A (de) |
| CN (1) | CN1238018A (de) |
| AT (1) | ATE212083T1 (de) |
| AU (1) | AU4225297A (de) |
| BR (1) | BR9711533A (de) |
| CA (1) | CA2266586A1 (de) |
| CZ (1) | CZ103199A3 (de) |
| DE (1) | DE69709663T2 (de) |
| EA (1) | EA199900323A1 (de) |
| HU (1) | HUP9903833A2 (de) |
| IL (1) | IL129087A0 (de) |
| NL (1) | NL1004094C2 (de) |
| NO (1) | NO991379L (de) |
| PL (1) | PL332374A1 (de) |
| SK (1) | SK39099A3 (de) |
| TR (1) | TR199900643T2 (de) |
| WO (1) | WO1998012376A1 (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2801594B1 (fr) * | 1999-11-25 | 2003-08-15 | Hoechst Marion Roussel Inc | Polyphenoxydendrimeres colores, nouveaux supports solubles, leur procede de preparation et leur utilisation en synthese organique |
| JP2003522266A (ja) | 2000-02-09 | 2003-07-22 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | ハイパーブランチ両親媒性ポリマー添加剤及び増加された表面エネルギーを有するポリマー組成物 |
| US6497959B1 (en) | 2000-03-30 | 2002-12-24 | General Electric Company | Use of dendrimers as a processing aid and surface modifier for thermoplastic resins |
| US20030135195A1 (en) * | 2002-01-16 | 2003-07-17 | Oscar Jimenez | Highly lubricious hydrophilic coating utilizing dendrimers |
| US7166657B2 (en) * | 2002-03-15 | 2007-01-23 | Eastman Kodak Company | Article utilizing highly branched polymers to splay layered materials |
| US6784267B1 (en) | 2002-07-25 | 2004-08-31 | Nalco Company | Polymers containing hyperbranched monomers |
| DE10318584A1 (de) * | 2003-04-24 | 2004-11-11 | Basf Ag | Hochverzweigte polymere Stabilisatoren |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB960798A (en) * | 1962-02-02 | 1964-06-17 | Montedison Spa | Improving the tinctorial properties of synthetic polymeric articles |
| US3361843A (en) * | 1964-06-15 | 1968-01-02 | Uniroyal Inc | Method of dyeing a blend of a polyolefin and a nitrogen containing polymer by using a dyebath containing lewis acids |
| US4631337A (en) * | 1983-01-07 | 1986-12-23 | The Dow Chemical Company | Hydrolytically-stable dense star polyamine |
| WO1995002008A1 (en) * | 1993-07-08 | 1995-01-19 | Dsm N.V. | Process for the preparation of a dendritic macromolecule |
| EP0672703A1 (de) * | 1994-03-16 | 1995-09-20 | Dsm N.V. | Herstellung von sternförmigen Polymeren |
| US5527524A (en) * | 1986-08-18 | 1996-06-18 | The Dow Chemical Company | Dense star polymer conjugates |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5530092A (en) | 1992-01-13 | 1996-06-25 | Dsm N.V. | Dendritic macromolecule and the preparation thereof |
-
1996
- 1996-09-23 NL NL1004094A patent/NL1004094C2/nl not_active IP Right Cessation
-
1997
- 1997-09-22 AU AU42252/97A patent/AU4225297A/en not_active Abandoned
- 1997-09-22 CZ CZ991031A patent/CZ103199A3/cs unknown
- 1997-09-22 AT AT97940486T patent/ATE212083T1/de not_active IP Right Cessation
- 1997-09-22 EA EA199900323A patent/EA199900323A1/ru unknown
- 1997-09-22 JP JP10514540A patent/JP2001502015A/ja active Pending
- 1997-09-22 WO PCT/NL1997/000527 patent/WO1998012376A1/en not_active Ceased
- 1997-09-22 CA CA002266586A patent/CA2266586A1/en not_active Abandoned
- 1997-09-22 CN CN97199797A patent/CN1238018A/zh active Pending
- 1997-09-22 DE DE69709663T patent/DE69709663T2/de not_active Expired - Fee Related
- 1997-09-22 TR TR1999/00643T patent/TR199900643T2/xx unknown
- 1997-09-22 HU HU9903833A patent/HUP9903833A2/hu unknown
- 1997-09-22 SK SK390-99A patent/SK39099A3/sk unknown
- 1997-09-22 PL PL97332374A patent/PL332374A1/xx unknown
- 1997-09-22 BR BR9711533A patent/BR9711533A/pt not_active Application Discontinuation
- 1997-09-22 IL IL12908797A patent/IL129087A0/xx unknown
- 1997-09-22 EP EP97940486A patent/EP0927275B1/de not_active Expired - Lifetime
-
1999
- 1999-03-22 NO NO991379A patent/NO991379L/no not_active Application Discontinuation
- 1999-03-23 US US09/275,140 patent/US6232378B1/en not_active Expired - Fee Related
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB960798A (en) * | 1962-02-02 | 1964-06-17 | Montedison Spa | Improving the tinctorial properties of synthetic polymeric articles |
| US3361843A (en) * | 1964-06-15 | 1968-01-02 | Uniroyal Inc | Method of dyeing a blend of a polyolefin and a nitrogen containing polymer by using a dyebath containing lewis acids |
| US4631337A (en) * | 1983-01-07 | 1986-12-23 | The Dow Chemical Company | Hydrolytically-stable dense star polyamine |
| US5527524A (en) * | 1986-08-18 | 1996-06-18 | The Dow Chemical Company | Dense star polymer conjugates |
| WO1995002008A1 (en) * | 1993-07-08 | 1995-01-19 | Dsm N.V. | Process for the preparation of a dendritic macromolecule |
| EP0707611A1 (de) * | 1993-07-08 | 1996-04-24 | Dsm Nv | Verfahren zur herstellung von einer dentrischen macromolekule |
| EP0672703A1 (de) * | 1994-03-16 | 1995-09-20 | Dsm N.V. | Herstellung von sternförmigen Polymeren |
Non-Patent Citations (1)
| Title |
|---|
| GUPTA B D ET AL: "DYEABLE POLYPROPYLENE COMPOSITION", REVIEW OF PROGRESS IN COLORATION & RELATED TOPICS, vol. 19, 1 January 1989 (1989-01-01), pages 7 - 19, XP000105445 * |
Also Published As
| Publication number | Publication date |
|---|---|
| ATE212083T1 (de) | 2002-02-15 |
| IL129087A0 (en) | 2000-02-17 |
| CA2266586A1 (en) | 1998-03-26 |
| EA199900323A1 (ru) | 1999-12-29 |
| PL332374A1 (en) | 1999-09-13 |
| HUP9903833A2 (hu) | 2000-04-28 |
| NO991379D0 (no) | 1999-03-22 |
| TR199900643T2 (xx) | 1999-09-21 |
| US6232378B1 (en) | 2001-05-15 |
| EP0927275A1 (de) | 1999-07-07 |
| EP0927275B1 (de) | 2002-01-16 |
| AU4225297A (en) | 1998-04-14 |
| DE69709663T2 (de) | 2002-10-17 |
| WO1998012376A1 (en) | 1998-03-26 |
| DE69709663D1 (de) | 2002-02-21 |
| CN1238018A (zh) | 1999-12-08 |
| JP2001502015A (ja) | 2001-02-13 |
| CZ103199A3 (cs) | 1999-09-15 |
| SK39099A3 (en) | 2000-03-13 |
| NO991379L (no) | 1999-05-21 |
| BR9711533A (pt) | 1999-08-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NL1001753C2 (nl) | Samenstelling omvattende een kunststof en een additief. | |
| US6444758B2 (en) | Hyperbranched amphiphilic polymeric additives and polymer compositions with increased surface energy | |
| NL1004094C2 (nl) | Werkwijze voor het opnemen van een aktieve stof in een kunststofvormdeel. | |
| DE69617461T2 (de) | Cinnamamide und deren verwendung als stabilisatoren | |
| WO2002046503A1 (en) | Dyeable polyolefin fibers and fabrics | |
| CA2249005A1 (en) | Light and thermally stable polyamide | |
| JP4117836B2 (ja) | ヤーン、ファイバー及びフィラメントの製造方法 | |
| MXPA99002763A (en) | Process for incorporating an active substance in a moulded plastic part | |
| CA2546351C (en) | Pre-fiber gel compositions and materials, methods of manufacture and uses thereof | |
| US3661821A (en) | Resinous condensation products and method of preparing same | |
| EP2272892B1 (de) | Verfahren zur herstellung von verbundstoffvorläufern | |
| DE2061062C3 (de) | Verbesserung der Anfärbbarkeit von Polyolefinen | |
| DE1469105C (de) | Textilfaden oder fasern aus einem Gemisch aus Olefinpolymeren ider Acryl nitrilpolymeren mit einer basichen poly meren Stickstoffverbindung sowie Ver fahren zur Herstellung dieser Textil faden oder fasern | |
| CN115103870A (zh) | 耐沾污支化聚酰胺 | |
| DE3924681A1 (de) | Verfahren zur beschleunigten festphasennachkondensation von polyamiden | |
| DE1469110B (de) | Textilfaden mit verbesserter Anfarb barkeit und Verfahren zu ihrer Herstellung |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PD2B | A search report has been drawn up | ||
| VD1 | Lapsed due to non-payment of the annual fee |
Effective date: 20010401 |