TW213934B - - Google Patents
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- Publication number
- TW213934B TW213934B TW080107354A TW80107354A TW213934B TW 213934 B TW213934 B TW 213934B TW 080107354 A TW080107354 A TW 080107354A TW 80107354 A TW80107354 A TW 80107354A TW 213934 B TW213934 B TW 213934B
- Authority
- TW
- Taiwan
- Prior art keywords
- ethylene
- propylene
- olefin
- copolymer
- item
- Prior art date
Links
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 95
- 239000005977 Ethylene Substances 0.000 claims description 95
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 53
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 52
- 229920001577 copolymer Polymers 0.000 claims description 37
- 238000006116 polymerization reaction Methods 0.000 claims description 37
- 150000001875 compounds Chemical class 0.000 claims description 34
- 229920000098 polyolefin Polymers 0.000 claims description 30
- 239000004711 α-olefin Substances 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 26
- 239000000178 monomer Substances 0.000 claims description 26
- -1 propylene, ethylene Chemical group 0.000 claims description 25
- 239000000126 substance Substances 0.000 claims description 22
- 150000001336 alkenes Chemical class 0.000 claims description 14
- 239000000758 substrate Substances 0.000 claims description 13
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 12
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 12
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 0.000 claims description 9
- 239000000779 smoke Substances 0.000 claims description 9
- 238000011049 filling Methods 0.000 claims description 8
- 229920001519 homopolymer Polymers 0.000 claims description 7
- 229920005606 polypropylene copolymer Polymers 0.000 claims description 7
- 239000007787 solid Substances 0.000 claims description 6
- 150000001993 dienes Chemical class 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 3
- 229920001384 propylene homopolymer Polymers 0.000 claims description 3
- 229920001897 terpolymer Polymers 0.000 claims description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- XTFIVUDBNACUBN-UHFFFAOYSA-N 1,3,5-trinitro-1,3,5-triazinane Chemical compound [O-][N+](=O)N1CN([N+]([O-])=O)CN([N+]([O-])=O)C1 XTFIVUDBNACUBN-UHFFFAOYSA-N 0.000 claims 3
- 239000002184 metal Substances 0.000 claims 3
- 229920005684 linear copolymer Polymers 0.000 claims 2
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- 239000012071 phase Substances 0.000 description 20
- 239000007789 gas Substances 0.000 description 17
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 15
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 15
- 239000008096 xylene Substances 0.000 description 15
- 239000003054 catalyst Substances 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 8
- 229910010165 TiCu Inorganic materials 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 229920001169 thermoplastic Polymers 0.000 description 7
- 239000004416 thermosoftening plastic Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012467 final product Substances 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 229920005604 random copolymer Polymers 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000011949 solid catalyst Substances 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical class [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 3
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Natural products OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 229920000092 linear low density polyethylene Polymers 0.000 description 2
- 239000004707 linear low-density polyethylene Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- 241001164374 Calyx Species 0.000 description 1
- 241000258920 Chilopoda Species 0.000 description 1
- 241001454694 Clupeiformes Species 0.000 description 1
- 229910052692 Dysprosium Inorganic materials 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000610361 Eurya Species 0.000 description 1
- 240000008620 Fagopyrum esculentum Species 0.000 description 1
- 235000009419 Fagopyrum esculentum Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 101001034845 Mus musculus Interferon-induced transmembrane protein 3 Proteins 0.000 description 1
- 244000131316 Panax pseudoginseng Species 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 101150069124 RAN1 gene Proteins 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 238000002083 X-ray spectrum Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 235000019513 anchovy Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- XMIIGOLPHOKFCH-UHFFFAOYSA-N beta-phenylpropanoic acid Natural products OC(=O)CCC1=CC=CC=C1 XMIIGOLPHOKFCH-UHFFFAOYSA-N 0.000 description 1
- GJRRTUSXQPXVES-UHFFFAOYSA-N bis(2-methylpropyl) oxalate Chemical compound CC(C)COC(=O)C(=O)OCC(C)C GJRRTUSXQPXVES-UHFFFAOYSA-N 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000009172 bursting Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000000658 coextraction Methods 0.000 description 1
- 230000002079 cooperative effect Effects 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- ZVMRWPHIZSSUKP-UHFFFAOYSA-N dicyclohexyl(dimethoxy)silane Chemical compound C1CCCCC1[Si](OC)(OC)C1CCCCC1 ZVMRWPHIZSSUKP-UHFFFAOYSA-N 0.000 description 1
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 1
- WOUUFVMQNDKHSY-UHFFFAOYSA-N dimethoxy(methyl)silane Chemical compound CO[SiH](C)OC WOUUFVMQNDKHSY-UHFFFAOYSA-N 0.000 description 1
- DWYGLGYVAMEOSL-UHFFFAOYSA-N dimethoxy(pentyl)silane Chemical compound CCCCC[SiH](OC)OC DWYGLGYVAMEOSL-UHFFFAOYSA-N 0.000 description 1
- VHPUZTHRFWIGAW-UHFFFAOYSA-N dimethoxy-di(propan-2-yl)silane Chemical compound CO[Si](OC)(C(C)C)C(C)C VHPUZTHRFWIGAW-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- KBQHZAAAGSGFKK-UHFFFAOYSA-N dysprosium atom Chemical compound [Dy] KBQHZAAAGSGFKK-UHFFFAOYSA-N 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 235000013601 eggs Nutrition 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- MDOAAHGPXOGVQG-UHFFFAOYSA-N ethene;propane Chemical group C=C.CCC MDOAAHGPXOGVQG-UHFFFAOYSA-N 0.000 description 1
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000021060 food property Nutrition 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 238000009863 impact test Methods 0.000 description 1
- 210000000936 intestine Anatomy 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 208000030175 lameness Diseases 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000008450 motivation Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 229910052704 radon Inorganic materials 0.000 description 1
- SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- NETBVGNWMHLXRP-UHFFFAOYSA-N tert-butyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C(C)(C)C NETBVGNWMHLXRP-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
- ZNOCGWVLWPVKAO-UHFFFAOYSA-N trimethoxy(phenyl)silane Chemical compound CO[Si](OC)(OC)C1=CC=CC=C1 ZNOCGWVLWPVKAO-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Description
經濟部屮央伐準工消fr合作杜印^ 五、發明説明(T ) 本發明係Μ於熱塑性膜、 擠出物質,及由烯烴聚合物 之摻合物_得之辑或片。 在許多讚S用上♦如食品 蕖用途包裝,工業上需要具 包装上* _需具有高剌孔抗 氣體及/或蒸氣之減少滲透 料之容器之膜需具有高剌孔 性及抗化學品性。用以《藥 刺孔抗性,低横數,高撕裂 由乙烯聚合物製得之_, 1 ,如丙烯之结晶均聚物及丙 提供此種所需性筲之姐合。 已嘗試《著製備结晶性丙 在立體特異性之齊格勒-那 8至25%彈性丙烯-乙烯共聚 點。然而,此種多相姐合物 撕裂強度或粗梭表面之形成 因此,霈要一種具有較低 裂強度•及所有其他所需性 本申謫茱中所用之所有份 有說明,周溫或室溫均為25 本發明提供一檷具有所需 構成之多相烯烴聚合物姐合 片及層壓片•及由其形成之共 姐合物與其他烯烴聚合物物質 包装 化學品及有害_質及醫 有特定性質之膜。例如在食品 性,高透明度及光澤度•及對 性。用Μ製造化學品及有害《 抗性,高拉伸強度•高撕裂抗 用途之膜,如血袋,需具有高 抗性及可高壓煮性。, $0 HDPE及LLDPE ,及丙烯聚合物 烯與乙烯之無規共聚物,無法 r 烯聚合物之多相混合物及藉著 塔型催化劑存在下依序聚合之 物•而可克眼此等聚合物之缺 之_會有魚眼形成,不«當之 Ο 撓曲横數,高透明度·良好撕 質之聚合物物質。 及百分比均以重壘計》除非另t: ° 性《之热塑性黑,包括由下列 物: (-先間-背二之注意事項扑填"本頁) 本紙張尺度蟓拓中a S家樣準(CNS)甲4規格(210x297公 2ί·以 Λ 6 I? 6 五、發明説明(2 ) (請先間-背而.-注-事項洱塡寫木頁) (a )約.10至50份之具有大於80之等規指數之丙烯均聚物 ,或選自下列姐群之共聚物:(i )丙烯及乙烯;(ii)丙烯 -乙鳔及CH2 = CHR σ -惮《,其中R為C2-,直鍵或支觭烷基 ,及(il?)丙烯及在(a ) ( ?〇中定義之α ·眾涇;該共眾物 含有大於80%丙烯且具有大於80之等規指數; (b) 約5至20份之半结晶且本質上缭性之共聚物鎇份· 其具有約20至60%之结晶度*其中共聚物係S自下列姐群 :U )乙烯及含超遇55%乙烯之丙烯;(ϋ)乙烯•丙烯* 及(a )(ii)中所定義之含1至10% α-烯烴·且超遇55%之 乙烯及ct-烯烴兩者之α-烯烴,及(iii)乙烯及(a)(ii)中 定義之含超遇55%之該α-烯烴之該α-烯煙;其中共聚物 在室溫或周溫時不溶於二甲苯;及 (c) 約40至80份之共聚物皤份,係選自下列组群之共聚 物:(i )乙烯及丙烯,其中共聚物含有約20至40%之乙嫌 經濟部+央找準而Π工消"合作杜印虹 ,及(》)乙烯,丙烯•及(a)(ii)中定義之《 -稀經其中 ct-烯烴存在量為1至10%,且乙烯及烯烴之最為20呢 至40% *及(iii)乙烯及(a )(ii )定義之含20至40% « - # 烴之α -烯烴,及任意含有0 . 5至10%之二烯*該共聚物 皤份在周溫時可溶於二甲苯,且具有1·5至4.〇dl/g之待性 黏度: 但以烯烴聚合物组合物之漶重為準’ (b)及"(C )皤份缌璽約為50%至90% ·且(b)/(c)之重藎比例為低 於0.4。本發明之另一具《例係搮供包括有晻用至热塑性 、|縝物w或金鼷基材之至少一表面之一曆多相烯逸聚合物姐 、. 合物之K。 本紙張尺度和»1中as家《準(CNS)T4規格(2丨0X297公46J)- ---1 ---1 Λ 6 η c 2139** : 五、e明説明(3) (請先間-背而之注-卞項再填艿本頁) 另一具.《例係提供烯《聚合物姐合物及熱塑性物霣之描 合物所得之臢。 成份U )較好存在5為〗0至份,悬好為20至3·5份。# (a)為丙烯.¾¾¾時,笱規抱效較钌為約85至98 ·遂ί.ς )為共聚物時,共聚物中丙烯之量較好約為90至9996。 成份(b)較好存在悬為7至15份,一般结晶性Κ»差掃 瞄卡計(DSC)测得約為20至60% ;通常,當同時使用乙烯 及該α-烯烴時,乙烯或該ct-烯烴含量或乙烯與該α -烯 烴坦合量為大於55%至98%,較好為80至95%。 成份(c )較好存在之量為50至70份,成份(c ).之乙烯或 該ct -烯烴含量或乙烯及該ct -烯烴之含量較好為20至38% ,最好為25至38% *當成份(c )為三聚物時•該α -烯煙 —般存在量為1至10%,較好為1至5%。較佳之固有黏度 為 1.7至 3dl/g 。 以烯烴聚合物姐合物缌重為準,(b)及(c)之》量較好 為65至80%,且(b)/(c)之重量比例較好為0.1至約0.3 〇 經濟部屮央標準一:ΓΑ工消伢合作社印製 當在烯烴聚合物姐合物中均存在有乙烯及ct -烯烴時, 乙烯單元或該α-烯烴單元*或乙烯及該ct-烯«單元之3« 量約為15%至35%。 此姐合物以DSC测定·在高於120它之溫度至少具有一僩 熔融峰,且在-10t及-35t:之《度下,相對於玻璃«穿透 度,存在有至少一偭峰。 此外,此等姐合物具有小於150 MPa之搞曲播数·通常為 本紙張尺·度UP中國S家楳準(CNS)甲4規怙(210x297公# - Λ 6 15 6 M濟部屮央伐準χ;!ίχ工消1V'合作社印3i 五、發明説明(4) 20及lOOHPa之間;產生時之張力強度為1〇至20 MPa,破裂 時伸長度超壜400 % ;在75%應力時,張力姐為20%至 5(^ ;蕭£ D硬度為MS H月當在-50 t:進行艾X图口 衝擊試驗跨不會醎裂(釔餡裂费运失败)° 較好獨S值低於40%,最好低於35%。 丙烯及乙烯或ct-烯烴,或丙烯.乙烯及α-烯斑之共聚 物或三聚物Μ成份(a)表示,且丙烯輿乙烯或與α_烯烴 之共聚物最常以成份(a)表示,偽由於其可提供具有較高 透明度之姐合物。 式CH2 = CHR之迪宜ct-烯烴包含丁烯-1,戊烯-1/ 4-甲基 戊烯-1,己烯-1及辛烯-1;當用以製備成份U)時’其存 在之量為使所得聚合物之等規指數不小於80% ° 當二烯在製備成份(b)及(c )之《程中存在時’ 一般為 丁二烯,1,4-己二烯,1,5-己二烯*亞乙烯原冰片二烯單 體,且一般存在量為0.5至10%,較好為1至5%。 此姐合物可»包括至少兩階段之聚合反應法製衡’其中 ,第一·階段中,使丙嫌或丙稀與乙稀,或該of -摊想或丙 摊,乙嫌或該of -燦烴聚合而形成成份(a),且在接下來 階段中,使乙烯及丙烯或該α -烯烴或乙烯,丙烯及該α _摊經及任意之二烯之混合物聚合而形成成份(b)及(c )° 聚合反縻可使用倨別反應器•在液相,氣相或液-氣相 中進行.所有均可以批式或連鱭式進行。例如,可使用液 M丙嫌作為稀釋劑進行成份(a )之聚合反懕•且在氣相中 (請先閲讀背',../之汰意事項洱填筠本頁) 裝_ 訂 線- ^^s7f4miS(21〇x297^_ 經濟部屮央標準,^π工消作合作社印31 :___—丨m_五、發明説明(5 ) 之成份(b )及(c )之聚合反應可M不需要進行中間物階段 ,除了丙烯之部份去除氣《之外,此為較佳之方法。 聚合反應在惰性氛霑中,在惰性《密劑’或液態或薷態 '皋遠存在下逵行, 適宜之憤性烴溶_包含飽和烴,如丙烷· 丁烷’己烷及 庚烷。 氫氣可依需要添加作為鐽轉移劑•以控制分子量。 成份(a)之聚合反應及成份(b )及(c )之聚合反應滬度 可為相同或不同,且通常為“^至⑽^,對成份(a)之聚 合反應而言,較好為50至80X:,對成份(b)及(c,)之聚合 反應而言·較好為40至651C。 若成份(a)之聚合反懕係在液態單體中進行時•反懕壓 力為使得在所用搡作溫度下,會與液態丙烯之蒸氣懕產生 競爭之壓力•最後Μ用Μ飼入催化劑混合物之少量情性稀 釋劑,及任意單《之《度壓力及使用作為分子最調節劑之 氲氣之蒸氣壓修正。 成份(b)及(c)之聚合反應若在氣相中進行時,其壓力 可為5至30ata;相對於兩階段之駐留時間,係視皤份(a )及(b) + (c)之所需比值而異,且通常為15分鐘至8小時 Ο 聚合反應中所用之催化劑包括下列之反應產物:⑴含有 含鹵索呔化合物及支撐於活化氯化鎂之霣子給予《化合物 (内部給予«)之固體成份,⑵不含鹵素之A1-三烷基化 合物,及⑶《子給予《化合物(外來給予雅)° 本紙張尺度和|1中國Β家樣準(CNS)甲4規格(210x297·:^- ..w; ____ Π 6_ 五、發明説明(6 ) «宜之呔化合物包含具有至少一®Ti-鹵素鐽者,如呔 之鹵化物及烷氧鹵化物。 泠了《洱貝有离萼《密«之可球型_粒形才之此等 烯頌聚忘物姐成谂·固蜎僂(L费成份需具声(c.)表两稹士· 於100 tf/g,較好介於50至δΟιπ2/^之間,(b)孔隙度為 0.25至0.4 oc/g,及(c)X-射線光譜,其中氣化鎂反射顥 示在2又〆角度為33. 5°及35°之間存在有鹵基.而在 14.95°之2以反射則不存在有鹵基,符號7_5^=布雷格角度 Ο 固體催化劑成份係»著形成二氱化鎂與酵之加辨物而製 備,酵類如乙酵,丙酵,丁酵及2-乙基己酵;每一莫耳 MgCU通常含3莫耳之醇,接著乳化此加成物,快速冷卻此 乳液,以引起加成物固化成球形顆粒,且薄逐渐由501增 溫至130Ό —段足Μ使每莫耳MgCU中酵含蛋由3其耳降至 1-1.5莫耳之時間,而使顆粒化加成物部份去酵化。部份 去酵化加成物接著在0¾下懸浮於TiCU中,使加成物對 TiCU濃度為40-50 g/1 TiCU,混合物接著加熱至8〇υ -1 35 υ之溫度1至2小時;當溫度達40 1C時,加入足量之® 子給予體,而獲得所需之Mg對霣子姶予體之莫耳比例。 經濟部屮央榀準局Π工消费合作杜印5i (請先閲^背而之.注*事項孙塡寫本頁) 加至TiCU之《子給予«化合物較好埋自呔酸烷_ •瓖 烷酯及芳酯•例如呔酸二異丁酯•二正丁醅,及二正辛酯 〇 當热處理階段结束時,以遇濾或沈澱作用分艫出過量之 热TiCU,且以Tic “之處理重覆一或多次,固《接著以遘 本紙張尺度中《國家樣準(CNS)肀4規格(210x297公 2139 五、發明説明(7 ) 經濟部屮央桴準::τ Λ工消伢合作社印¾. 當地惰性.烴化合物如己烷或庚烷洗滌’並乾埽。 一般固體催化劑成份具有下列特徴: 巧萏稹:小於¥ /s,較好介於5〇及Ww* 之.間· 孔隙度:0 . 2 5 -. 4 r ’s 孔陈體積分佈.· 50%之孔隙具有大於1〇〇€之半徑 X-射埭騙繒:氯化鎂反射處顧示在33.5°及35°之2又/角 之間具有極大值之鹵基強度•且在14.95°之2以角則無反 射。 播著使固《催化繭成份與三烷基鋁化合物*較好為三乙 基鋁及三異丁基鋁•及轚子給予體化合物混合而揮得催化 各種電子給予膀化合物為本技·已知者f較佳之《子給 予Si化合物為具有R' R" Si(0R)2之矽烷化合物,式中〆 及R"可為相同或不同,且為CKe直鍵或支鍵烷基, Cs-ΐβ環综基或0〇-18芳基’且R為Cl-4烧基。 可使用之一般矽烷化合物包含二苯基二甲氧基矽烷•二 環己基二甲氧基矽垸•甲基第三丁基二甲氧基矽烷.二異 丙基二甲氧基矽烷,二環戊基二甲氧基矽烷,環己基甲基 二甲氧基矽烷,及苯基三甲氧基矽烷。 Al/Τί比值一般介於10及200間,且A1/矽烷莫耳比值介 於1/1及1/100間。 催化劑可預先與少量之烯烴單《接《(預聚合反應), 维持催化劑在煙溶劑中之懸浮態•並在室溫至60 t之溫度 聚合足以產生催化劑重量之0.5至3倍之聚合物量之時間。 (請先閲1?背,?之注意事項祚塥寫木S) 裝- 訂- 線· 本紙張尺度埃JP中HS家樣毕(CNS)甲4規格(210x297公 t〇lf ΛDu Yin ^ Cooperation of the Ministry of Economic Affairs and the Ministry of Economic Affairs and Development fr. V. DESCRIPTION OF THE INVENTION (T) The present invention is based on thermoplastic films, extruded materials, and blends or tablets obtained from blends of olefin polymers. It is used in many applications such as food packaging, which needs to be packaged in industry * _The film of the container with a high puncture resistance to gas and / or vapor reduction permeable materials needs to have high puncture resistance and chemical resistance Sex. Used for "drug puncture resistance, low transverse number, high tear" made from ethylene polymer, 1, such as crystalline homopolymer of propylene and propylene to provide this kind of desired combination. Attempts have been made to prepare crystalline propylene at the stereospecific Ziegler-Na 8 to 25% elastic propylene-ethylene copolymerization point. However, the tear strength of this heterogeneous sister compound or the formation of the surface of the thick shuttle. Therefore, the centipede has a lower tear strength and all other required properties. All the parts used in this application are explained, Zhou Wen or The room temperature is 25. The present invention provides a heterophasic olefin polymer laminate sheet and laminate sheet having the desired composition, and a co-former compound formed therefrom and other olefin polymer substances. Packaging chemicals and harmful substances And medicine has a specific nature of the film. For example, in food properties, high transparency and gloss and contrast. The use of Μ to manufacture chemicals and harmful "resistance, high tensile strength • high tear resistance film, such as blood bags, need to have high resistance and autoclavability. , $ 0 HDPE and LLDPE, and random copolymers of propylene polymer olefin and ethylene, heterogeneous mixtures of olefin polymers and those that are polymerized sequentially in the presence of tower catalyst The shortcomings_ there will be fisheye formation, not «as is. Ο deflection horizontal number, high transparency, good tear quality polymer material. And percentages are calculated in terms of heavy barriers, unless otherwise t: ° Thermoplastic black, including the following: (-first time-remarks on the second page fill in " this page). Sample standard (CNS) A 4 specifications (210x297 male 2ί · Λ 6 I? 6 V. Description of the invention (2) (please first-back.-Note-matters to write wooden pages in Ercheng) (a) about .10 Up to 50 parts of a propylene homopolymer with an isotactic index greater than 80, or a copolymer selected from the following sister groups: (i) propylene and ethylene; (ii) propylene-ethane bladder and CH2 = CHR σ- 殮 ", Where R is C2-, straight bond or branched alkyl, and (il?) Propylene and α defined in (a) (? 〇 · Zhongjing; the common object contains greater than 80% propylene and has greater than 80 Isotactic index; (b) About 5 to 20 parts of semi-crystalline and intrinsically volatile copolymer. It has a crystallinity of about 20 to 60% * wherein the copolymer is S from the following sister group: U) Ethylene And propylene containing 55% ethylene overrun; (ϋ) ethylene • propylene * and 1 to 10% α-olefins as defined in (a) (ii) and both 55% ethylene and ct-olefin overrun Α-olefin, and the content defined in (iii) ethylene and (a) (ii) Encountering 55% of the α-olefin smoke of the α-olefin; wherein the copolymer is insoluble in xylene at room temperature or ambient temperature; and (c) about 40 to 80 parts of the copolymer are selected from the following groups Copolymer: (i) Ethylene and propylene, where the copolymer contains about 20 to 40% of the second suspected Ministry of Economic Affairs + Central Accuracy and Π Industry Consumer " Cooperative Du Yinhong, and (》) Ethylene, Propylene and (a) ( ii) as defined in "-Dilute Jing where ct-olefins are present in an amount of 1 to 10%, and ethylene and olefins are the most 20 to 40% * and (iii) ethylene and (a) (ii) contain 20 to 40% «-# Hydrocarbon alpha-olefins, and optionally containing 0.5 to 10% of diene * This copolymer is soluble in xylene at ambient temperature and has a ratio of 1.5 to 4.0 dl / g Dependent viscosity: but subject to the weight of the olefin polymer composition '(b) and "(C)" The seal is approximately 50% to 90% · and the weight ratio of (b) / (c) It is less than 0.4. Another example of the present invention is "K" which includes a multiphase heterogeneous polymer, which is a compound of at least one surface of a thermoplastic material, a thin material w or a gold base material. . This paper scale and the "as standard" (CNS) T4 Grid (2 丨 0X297 Gong 46J)---- 1 --- 1 Λ 6 η c 2139 **: Fifth, e-clear explanation (3) (please first-back note-Bian item and then fill this page ) Another tool. "The example is provided by the description of the polymer compound and the thermoplastic compound. The component U) preferably exists 5 to 0 to 0 parts, and the suspension is 20 to 3.5 parts. . # (a) is propylene. When the amount of propylene in the copolymer is about 85 to 98 · sui.ς when compared to ruthenium, the amount of propylene in the copolymer is preferably about 90 to 9996. The component (b) is preferably present in a suspension of 7 to 15 parts. Generally, the crystallinity K »differential scanning card meter (DSC) measures about 20 to 60%; usually, when both ethylene and the α-olefin are used at the same time, ethylene Or the content of the ct-olefin or the blending amount of ethylene and the α-olefin is greater than 55% to 98%, preferably 80 to 95%. The component (c) is preferably present in an amount of 50 to 70 parts. The content of ethylene or the ct-olefin or the content of ethylene and the ct-olefin in the component (c) is preferably 20 to 38%, and most preferably 25 to 38% * When component (c) is a terpolymer • The amount of α-ene smoke generally present is 1 to 10%, preferably 1 to 5%. The preferred intrinsic viscosity is 1.7 to 3dl / g. Based on the weight of the olefin polymer complex, the amount of (b) and (c) is preferably 65 to 80%, and the weight ratio of (b) / (c) is preferably 0.1 to about 0.3. Ministry Standard 1: Printed by ΓΑ 工 工 伢 Cooperative Society When ethylene and ct-olefin are present in the olefin polymer compound, ethylene unit or the α-olefin unit * or ethylene and the ct-ene «unit The amount of 3 «is about 15% to 35%. This sister compound is measured by DSC. It has at least one melting peak at a temperature higher than 120, and there is at least one peak at -10t and -35t: with respect to the glass penetration. In addition, these sister compounds have a play count of less than 150 MPa · Usually based on paper size · Degree UP China S Jiayu Standard (CNS) A 4 rules (210x297 公 #-Λ 6 15 6 M Jibu Central cutting standard χ;! Χχ 工 消 1V 'Cooperative printed 3i V. Description of the invention (4) Between 20 and 100 HPa; the tensile strength at the time of generation is 10 to 20 MPa, the elongation at break exceeds 400%; at 75 % Stress, the tension of the sister is 20% to 5 (^; Xiao £ D hardness is MS H month when at -50 t: the Ai X figure mouth impact test will not crack (the failure of yttrium filling cracking) fails ° Good S value is less than 40%, preferably less than 35%. Propylene and ethylene or ct-olefin, or propylene. Ethylene and α-ene spot copolymer or terpolymer M component (a), and propylene The copolymer of ethylene or α-olefin is most often expressed as component (a), because it can provide a sister compound with higher transparency. Formula CH2 = CHR's di-ct-olefin contains butene-1, pentene -1 / 4-methylpentene-1, hexene-1 and octene-1; when used to prepare component U) ', the amount present is such that the isotactic index of the resulting polymer is not less than 80% ° Diene is stored in the process of preparing ingredients (b) and (c) At the time 'is generally butadiene, 1,4-hexadiene, 1,5-hexadiene * vinylidene proborne norbornene monomer, and generally present in an amount of 0.5 to 10%, preferably 1 to 5 %. This sister compound may include at least two stages of polymerization reaction checks and balances' where, in the first stage, make acetone or acetone and ethene, or the of-share or ace, ace or equip. of-bearing hydrocarbons are polymerized to form the component (a), and in the next stage, ethylene and propylene or the α-olefin or ethylene, propylene and the α _ spreading and any mixture of diene are polymerized to form the component ( b) and (c) ° Polymerization reaction can be carried out using separate reactors • It can be carried out in liquid phase, gas phase or liquid-gas phase. All can be carried out in batch or continuous anchovy type. For example, liquid M can be used Used as a diluent for the polymerization reaction of the component (a) • and in the gas phase (please read the back first, ../regarding the intentions, fill in this page) _ _ ^^ s7f4miS (21〇x297 ^ _Ministry of Economics Standard, ^ π 工 工作 作 社 印 31: ___— 丨 m_ V. Invention Description (5) The polymerization reaction of the components (b) and (c) may not require an intermediate stage, apart from Partial removal of gas from olefins is the preferred method. The polymerization reaction is carried out in an inert atmosphere, in the presence of an inert "dense agent" or liquid or swollen state, suitable for indignant hydrocarbon dissolution_ Contains saturated hydrocarbons, such as propane, butane, hexane and heptane. Hydrogen can be added as a transfer agent if necessary to control molecular weight. Polymerization of component (a) and polymerization of components (b) and (c) The degree can be the same or different, and is usually "^ to ⑽ ^, for the polymerization reaction of component (a), preferably 50 to 80X :, for the polymerization reaction of components (b) and (c,) · Preferably it is 40 to 651C. If the polymerization reaction of component (a) is carried out in liquid monomer • The reaction pressure is such that at the operating temperature used, it will compete with the vapor pressure of the liquid propylene vapor • Finally, M is fed into the catalyst mixture A small amount of sentimental diluent, and the correction of the vapor pressure of the radon gas used as the most regulator of the molecule in any single book. When the polymerization reaction of components (b) and (c) is carried out in the gas phase, the pressure can be 5 to 30 ata; relative to the residence time of the two stages, it depends on the content of (a) and (b) + (c) The required ratio varies, and is usually 15 minutes to 8 hours. The catalyst used in the polymerization reaction includes the following reaction products: ⑴Containing halogen-containing cordierium compounds and supported by activated magnesium chloride give "compound (internal give« ), ⑵ halogen-free A1-trialkyl compounds, and ⑶ "sub-giving" compounds (externally given) ° the size of this paper and | 1 China BS family standard (CNS) A 4 specifications (210x297 · : ^-..w; ____ Π 6_ V. Description of the invention (6) «Yizin compound contains those with at least one ®Ti-halogen compound, such as halides and alkoxy halides. From the calyx "Dense« Globular_grain-shaped talents of this kind, the enchanting sister of the polyphony Cheng Cheng · Gusui (L fee component needs to have sound (c.) Table two Zhenshi · At 100 tf / g, It is preferably between 50 and δΟιπ2 / ^, (b) the porosity is 0.25 to 0.4 oc / g, and (c) the X-ray spectrum, in which the vaporized magnesium reflection is shown at 2 ° There is a halogen group between 33.5 ° and 35 °. However, there is no halogen group at 14.95 ° 2 by reflection, the symbol 7_5 ^ = Breg angle Ο solid catalyst component »the formation of magnesium dihydride and It is prepared by the addition of enzymes, such as yeast, propanase, butyrate and 2-ethylhexylase; each mole of MgCU usually contains 3 moles of alcohol, followed by emulsification of this adduct and rapid cooling of this Emulsion, to cause the solidification of the adduct into spherical particles, and the thickness gradually increased from 501 to 130Ό-a period of foot M to reduce the amount of fermented eggs per mole of MgCU from 3 ears to 1-1.5 moles. The granulated adduct is partially de-fermented. The partially de-fermented adduct is then suspended in TiCU at 0¾ so that the concentration of the adduct to TiCU is 40-50 g / 1 TiCU, and the mixture is then heated to 8 ° υ -1 35 The temperature of υ is 1 to 2 hours; when the temperature reaches 40 1C, add a sufficient amount of ® donor to obtain the required molar ratio of Mg to Jiazijia donor. Ministry of Economic Affairs The quasi-bureau Π industry consumer cooperation Du Yin 5i (please read ^ back to the first. Note * matters Sun Yat wrote this page) added to TiCU "sub-giving« compounds are better buried from oxalic acid alkyl _ • urethane ester and aromatic Ester • For example, diisobutyl oxalate • Di-n-butyl dibutylate, and di-n-octyl ester. When the heat treatment phase ends, excess hot TiCU is separated by filtration or precipitation, and repeated by Tic One or more times, and then follow the standard of the National Sample Standard (CNS) 4 (210x297 public 2139) in the paper standard. 5. Description of the invention (7) The standard issued by the Ministry of Economic Affairs: τ Λ 工 工 缢 cooperative print ¾. Locally inert. Hydrocarbon compounds such as hexane or heptane are washed and dried. General solid catalyst components have the following characteristics: Qiaolianzhen: less than ¥ / s, preferably between 50 and Ww *. Porosity Degree: 0. 2 5-. 4 r's pore volume distribution. · 50% of the pores have a radius greater than 100 € X-ray deception: Magnesium chloride reflection at 23.5 ° and 35 ° In addition, there is a maximum halogen group intensity between / angles and there is no reflection at an angle of 2 of 14.95 °. Broadcasting solid "catalyst cocoon component and trialkyl aluminum compound * preferably triethyl aluminum and tri isobutyl aluminum" and zizi donor compound mixed to catalyze various electrons to give the bladder compound technology Knowing that f is better, the "Si-donating Si compound is a silane compound having R 'R " Si (0R) 2, where 〆 and R " may be the same or different, and are Cke straight or branched alkyl groups, Cs- Ιβ ring complex or 0〇-18 aryl 'and R is Cl-4 burn group. Common silane compounds that can be used include diphenyl dimethoxy silane • dicyclohexyl dimethoxy silane • methyl tert-butyl dimethoxy silane. Diisopropyl dimethoxy silane, dicyclo Amyl dimethoxy silane, cyclohexyl methyl dimethoxy silane, and phenyl trimethoxy silane. The Al / Τί ratio is generally between 10 and 200, and the A1 / silane molar ratio is between 1/1 and 1/100. The catalyst can be pre-connected with a small amount of olefin (pre-polymerization) to maintain the suspension of the catalyst in the smoke solvent and polymerize at room temperature to 60 t to produce a polymer amount of 0.5 to 3 times the weight of the catalyst time. (Please read the notes of 1? Back, Zuo 塥 寥 木 S) Binding-Binding-Thread · This paper standard Egypt JP in the HS home sample (CNS) A 4 specifications (210x297 public t〇lf Λ
Λ 6 Π G 五、發明説明(8 ) (請先閱-訐而之-*事項孙場艿木頁) 此預聚合反應亦可在液體或氣態單H中進行•在此情況 下,可產生達催化_重量100倍悬之聚合物。 本發明熱酽巴眾烴聚合物由浑化劑殘留之含景及鼉篾小-至足以使S化爾殘贸物·'唸 < —般s示為尹灰化)為纪+ 必要之程度。 以上述催化餚製備之热塑性烯烴聚合物為球形顆粒狀, 且此顆粒具有0.5至7m之直徑。 除非另有說明,杏刖下列之分析方法係用以特》化此支 撐之催化_成份,多相烯烴聚合物姐合物*由其製供之膜 及比較例膜物質。 , 卞法_ 熔融流速· g/ΙΟ分鐘 乙稀 wt% 特性黏度 二甲苯溶解性,Wt% 在23υ之撓曲棋數及玻 璃轉移溫度 ASTM-D 1238 ,條件 L IR光_ 於135 t:之四氢莱中测定 參見下述 經濟部屮央橾準而Π工消仲合作社印 在1 Η z之頻率测量及2t:/分 鐘之掃描溫度下*使用聚合物 «驗室之DMTA動力機械澜量装 置•欲分析之聚合物樣品飾板 (4〇x l〇x 2ra)自 MCarver 應 縮製備之壓力棋製片上切下, K力棋製片係在200 1C下Μ 10噸壓力壓製10分鐘,接著在 1 5 1C /分鐘下冷卻此片而製得 本紙張尺度承BP中a B家標準(CNS) 規格(210x297公#〇 -Λ 6 Π G V. Description of the invention (8) (please read-讦 而 之-* Matters Sun Changyi page) This pre-polymerization reaction can also be carried out in liquid or gaseous single H • In this case, it can be produced Up to catalyzed_100 times the weight of suspended polymer. The content of the hot-hybrid public hydrocarbon polymer of the present invention remaining from the turbidity agent is small and small-enough to make the Shuaer residues. "Nian <-generally s shown as Yin Huihua) is necessary + necessary degree. The thermoplastic olefin polymer prepared by the above catalytic method is in the form of spherical particles, and the particles have a diameter of 0.5 to 7 m. Unless otherwise stated, Xingya's following analytical methods are used to specialize the catalytic component of this support, heterogeneous olefin polymer complexes * and the membrane materials prepared from them. , Bian method _ Melt flow rate · g / 10 minutes ethylene wt% intrinsic viscosity xylene solubility, Wt% deflection number at 23υ and glass transition temperature ASTM-D 1238, condition L IR light _ at 135 t: For the determination of tetrahydromethine, please refer to the following: The Ministry of Economic Affairs, the central government, and the Gonggongzhong Cooperative Society printed at a frequency of 1 Hz and a scanning temperature of 2t: / min * Use polymer «laboratory DMTA power machine capacity Device • The polymer sample trim (4〇xl〇x 2ra) to be analyzed was cut from the pressure chess piece prepared by MCarver shrinkage. The K force chess piece was pressed at 200 1C for 10 minutes under a pressure of 10 tons. Next, the sheet was cooled at 151 C / minute to prepare the paper standard BP standard (CNS) specification (210x297 公 # 〇-
五、發明説明(9) 艾氏懸莺衝擊 白?I 7 5 %之盂力组 ASTH-D 256 A STΜ - D I 0 0? ASTKD 412 產生時及破裂時之張力強度ASTM-D 638 產生時及破裂時之伸長度 ASTM-D 638 表面積 孔隙度 整體密度 光澤度 摩擦係數 溼蒸汽穿透度 挪鏢銜擊強度 除非另有說明 B.E.T. B . E.T. DIN-53194 ASTH-D 1922-78 ^ ASTM-D 1938-85 ASTM-D 523 ASTM-D 1984 ASTM-E 96 ASTM D 4272-83 否則欲進行各種物理機械分析之烯烴聚 (請先閲汸背而之ii意事項再堝寫本頁) 裝· 訂 線- 經濟部屮央標準/-JA工消许合作杜印1i 合物姐合物之樣品·係在將物質以0.1% I「ganox 1010肆 [亞甲基3,5-二第三-丁基-4-羥基氫肉桂酸酿)]甲烷及 0.1%BHT(2,6 -二第三丁基對甲酚)穩定化後,使用Neg「i 及Bossi 90射出壓縮機棋製•並以單蟋旋班達拉擠出機( 園苘直徑30·«)在210t:下製粒•分析條件如下: 熔融溫度 250 横製溫度 60它 射出時間 20秒 本紙ft尺度摩中SS家楳平(CNS)<F4規格(2U1X2D7公却I - -濟部屮央柃準而Π工消"合作杜印51V. Description of the invention (9) Ai's hanging warbler impact White? I 7 5% of the force group ASTH-D 256 A STM-DI 0 0? ASTKD 412 Tensile strength at the time of generation and rupture ASTM-D 638 Elongation at the time of generation and rupture ASTM-D 638 Surface area porosity overall density Gloss Coefficient of Friction Wet Vapor Penetration Dart Impact Strength Unless otherwise specified BET B. ET DIN-53194 ASTH-D 1922-78 ^ ASTM-D 1938-85 ASTM-D 523 ASTM-D 1984 ASTM-E 96 ASTM D 4272-83 Otherwise, the olefin polymerization for various physical and mechanical analysis (please read the contents of ii first and then write this page) Installation · Threading-Ministry of Economic Affairs Standard / -JA 工 消 许 合作 DU The sample of India 1i compound sister compound is based on 0.1% I "ganox 1010 [methylene 3,5-di-tert-butyl-4-hydroxyhydrocinnamic acid]] methane and 0.1% After stabilizing BHT (2,6-di-tert-butyl-p-cresol), the compressor is made using Neg "i and Bossi 90 injection compressors. • It is a single-cylinder screw extruder (Yuanbi diameter 30 ·« ) Granulation at 210t: The analysis conditions are as follows: Melting temperature 250 Horizontal temperature 60 It injection time 20 seconds This paper ft scale Mosaka SS Kazuhide (CNS) < F4 specification (2U1X2D7 public I-- Che Eurya central portion and Π station registration cancellation " printed cooperatives 51
: Λβ___lj_6_ 五、發明説明(〗〇) 冷卻時.間 2 5秒 欲進行白霧分析之樣品係使用GBF F 235/90射出壓製機 ,在下列條件下,横製成75X75X1 zs之飾板。 熔融溫度 2 6 0 t; 模製溫度40 射出時間 20秒 冷卻時間10秒 膜物質之樣品厚度為1密耳,並自縝Η上切成特定 ASTM測試方法中使用之大小。 (b )及(c )皤份總和之重量百分比,M%(b ),(c )表 示,係在第二階段中*以测定飼入混合物之重量而計算· 並與最終產物之重量比較。 本文所述之(a ),(b )及(c )皤份之重量百分比(%)之 測定如下: %(a)=100%_ [(b) + (c)] % (C )= Sr- P.S* 式中Sf及S·分別為最终產物及聚丙烯皤份(a )在二甲苯 中可溶部份之重悬百分比;Ρβ為該皤份與最終產物間之重 最比值。 %(b)=100-%(a)-%(c) 含於共聚物皤份(c)中可溶於二甲笨之乙烯或α -烯烴 或乙烯及該α -烯烴之重量百分比侏使用下列公式計算: 皤份(c )中乙烯及/或該cr-烯烴之 (Cr - C.) · X vt96 =- , 1 一 X (-先閲-背而之注-卞項洱碼艿木訂) 本紙張尺度贤|?1中881家標準((:吣)〒4規格(210乂297^^)2- Λ f; ii 6 五、發明説明(11) 式中Cf =最終產物在二甲苯中可溶之乙烯及/或該α -烯烴 % ; (: =餾伤(a )於二甲苯中可溶之乙烯及/或該<2-烯涇% ; X = S, · P«/Sf «份(c )之固有黏度(I.V.C。))係使用下列公式計算: (I.V. c〇>)=(I.V.sr-I.V. c-).X)/(l-X) 式中I.V.Sf為最終组合物之二甲苯可溶饑份之固有黏度 ,且I.V.(«〇為皤份(a )之二甲苯可溶部份之固有黏度。 在室溫下二甲苯可溶之烯烴聚合物组合物之重量百分比 之測定,係將2.5s之聚合物溶於250 之二甲苯中*且偽 於配有攪拌器之容器中•在135 t:下加熱攪動20分鐘;溶 液冷卻至25 1C,同時繼續攪動,然後在不攪動下使其靜置 30分鐘· K使固«沈降· Μ濾紙邊濾固體,殘留溶液以氮 氣流處理而蒸除,固《殘留物在8〇υ下真空乾烽直至達恆 重。室溫下不溶於二甲苯之聚合物之重量百分比為聚合物 之等規指數,於此方式中所得之值相當於經由Μ沸騰之正 庚烷萃取所期I定之等規抱數•其係定義為聚合物之等規指 數。 多相烯烴聚合物姐合物之例示*例•其物理性質*其製 備方法,以該烯烴聚合物姐合物為主之_ •及製備該膜之 方法均述於下。 因W催Yh蘭成份 本紙51尺度神?1中a國家楳準(CNS) 1M規tM210x2inq)3 - (請先閱-背而之注意卞項洱填艿本玎) 裝- 訂: Λβ ___ lj_6_ V. Description of the invention (〗 〇) Cooling time. 25 seconds. The sample to be analyzed for white fog is a GBF F 235/90 injection press. Under the following conditions, a 75X75X1 zs decorative panel is made horizontally. Melting temperature 2 6 0 t; Molding temperature 40 Injection time 20 seconds Cooling time 10 seconds The thickness of the film sample is 1 mil, and it is cut from the H to the size used in the specific ASTM test method. (b) and (c) The weight percentage of the sum of the ingredients, M% (b), (c) indicates that it was calculated in the second stage * by determining the weight of the feed mixture and compared with the weight of the final product. The weight percentage (%) of (a), (b) and (c) described in this article is determined as follows:% (a) = 100% _ [(b) + (c)]% (C) = Sr -PS * where Sf and S · are the resuspended percentages of the final product and the soluble portion of polypropylene (a) in xylene, respectively; Ρβ is the weight ratio between the final portion and the final product. % (B) = 100-% (a)-% (c) The content of ethylene or α-olefin or ethylene and the weight percentage of the α-olefin soluble in dimethyl stupid (c) contained in the copolymer fraction (c) Calculate by the following formula: (v-C.) of ethylene and / or the cr-olefins in Xuan (c) · X vt96 =-, 1 1 X (-read first-note to the back-Bian item Er code 艿 木 定) The size of this paper | 1 881 standards ((: 吣) 〒 4 specifications (210 297 ^^) 2- Λ f; ii 6 V. Description of the invention (11) where Cf = final product in xylene Soluble ethylene and / or the α-olefin%; (: = Distillate (a) ethylene soluble in xylene and / or the <2-enezine%; X = S, · P «/ Sf «Part (c) intrinsic viscosity (IVC.)) Is calculated using the following formula: (IV c〇>) = (IVsr-IV c-). X) / (lX) where IVSf is the final composition The inherent viscosity of the xylene soluble fraction, and the IV («〇 is the inherent viscosity of the xylene soluble fraction of (a). The weight percentage of xylene soluble olefin polymer composition at room temperature The determination was made by dissolving 2.5s of polymer in 250 xylene * and falsely in a container equipped with a stirrer • Heat and stir at 135 t for 20 minutes; the solution is cooled to 25 1C while continuing to stir, and then let it stand for 30 minutes without stirring. K allows solid «sediment *. Filter the solid while filtering the paper, and the residual solution is flowed with nitrogen After processing and evaporating, the residue is dried under vacuum at 80 ° C until it reaches a constant weight. The weight percentage of the polymer insoluble in xylene at room temperature is the isotactic index of the polymer, the value obtained in this way It is equivalent to the number of isotacticity determined by the extraction of n-heptane boiling through M. It is defined as the isotactic index of the polymer. Exemplary examples of heterogeneous olefin polymer compounds * Examples • Physical properties * Preparation method , Mainly based on the olefin polymer compound _ • and the method of preparing the film are described below. Because W urge Yh blue composition of the paper 51 scale God? 1 China a National Standard (CNS) 1M regulations tM210x2inq) 3 -(Please read first-pay attention to Bian Xianger fill in this book) Pack-book
Λ ( '; Η G 經濟部屮央桴準杓Α工消设合作社印31 五、發明説明(12) (A ) MgCU/酵加成物之製衡 在惰性氛围中,將28.4g無水MgCU,49.5 g無水乙酵’ l〇〇?d ROL 0B/30凡士林油及1〇〇«!!之具有350cs黏度之矽 油導入纪有攢拌器之反應容器中,技Μ油浴繅加热至 120t:,及攪拌直至MgCU溶解。接著在惰性氛圃中’將熱 反應混合物倒至配備有Ultra Turrax T-45 Η攪拌器及加 熱套苷,並含有150π1凡士林油及150*1矽油之1 500丨1容器 中。溫度維持在120t:並在3000「pa下攫拌3分鐘·此混合 物接著饋入配有攪拌器,且含有在無水冰/異烷浴中冷卻 至Ot之lOOOnl無水正庚烷之2升容器中*並在戶b /秒之 頂端速度下攪拌約20分鐘,同時溫度维持在OC,因而形 成之加成物顆粒Μ »濾回收*並在室溫下以500 η丨份之無 水己烷洗滌3次,並在氮氣中逐灌加热而將溫度自50C升 至100 t ·加熱時間為足以將每1舆耳HgCU中酵含董自3 莫耳降至1.5莫耳之時間。此加成物具有9.1 rf/g之表面 積及0 . 564 g/cc之整19密度。 (B)固體催化劑成份之製備 加成物(25g)在氮氣中,倒入配«有攪拌器且含有在 攪動之625b 1 TiCU之反應容器中,接著於1小時内加熱至 100 t:,當溫度達401時,加入肽酸二異丁酯,其鼉為使 Mg與酞酸二異丁酯之莫耳比例為8。容器之内容物在 100 C及攪動下加熱2小時•停止攪動並使固《沈降· K 虹吸管移除熱液《,將550 »1 TiCU加至容器中之固《内 ,且混合物在攢動下於120 =加热1小時,停止攪動使固» (-先閲-背而之注-事項件填艿木钉) 本紙5IL尺度两押中Λ ffl家樣準(CNS)甲4規ts(210x297:4)4 -Λ ('; Η G The Ministry of Economic Affairs, 汮 極 桴 杓 揓 術 sets up the cooperative cooperative seal 31 V. Description of the invention (12) (A) MgCU / enzyme adduct balance in an inert atmosphere, 28.4g anhydrous MgCU 49.5 g anhydrous ethyl yeast 'l〇〇? D ROL 0B / 30 petroleum jelly and 100〇 «!! The silicone oil with a viscosity of 350cs is introduced into the reaction vessel of the Jiyouji mixer, and the technical oil bath is heated to 120t: , And stir until the MgCU is dissolved. Then, in an inert atmosphere garden, 'pour the hot reaction mixture to an Ultra Turrax T-45 Η stirrer and heating mantle glycoside, and contains 150π1 petroleum jelly and 150 * 1 silicone oil 1 500 丨 1 In a container. Maintain the temperature at 120t: and stir at 3000 "pa for 3 minutes. This mixture is then fed with a stirrer and contains 100Onl of anhydrous n-heptane cooled to Ot in an anhydrous ice / isoane bath In a liter container * and stir for about 20 minutes at the top speed of b / sec, while maintaining the temperature at OC, so the formed adduct particles M »recovered by filtration * and at room temperature with 500 n The alkane was washed 3 times, and the temperature was gradually increased from 50C to 100 t by heating and filling in nitrogen. The heating time was enough 1 The time for the fermentation of HgCU to decrease from 3 mol to 1.5 mol. The adduct has a surface area of 9.1 rf / g and a density of 0.564 g / cc. (B) The composition of solid catalyst Prepare the adduct (25g) in nitrogen, pour into a reaction vessel equipped with a stirrer and containing 625b 1 TiCU under agitation, then heat to 100 t within 1 hour: when the temperature reaches 401, add the peptide Diisobutyl acid, the mole is such that the molar ratio of Mg to diisobutyl phthalate is 8. The contents of the container are heated at 100 C and agitated for 2 hours • Stop the agitation and let the solid "settling · K siphon move Remove the thermal fluid ", add 550» 1 TiCU to the container ", and the mixture is heated at 120 = 1 hour under storage, stop stirring to solidify» (-first read-back note-item filling Wooden pegs) 5IL standard two bets on this paper Λ ffl home sample standard (CNS) A 4 gauge ts (210x297: 4) 4-
Λ 6 η G 五、發明説明(i 3) 沈降接著以虹吸管移除热體,固在在60i〇下以200ml份 數之無水己燒清洗6次,接著在室溫清洗3次,真空乾堍後 -之固體具有〇.261c>c/!?之孔隙度H5 #/g之表面镄及 0. 44.fi/cc整體密度。 奮例1 - 3 明多相烯烴聚合物姐合物及製備此聚合物之 方法。 一般搡作始 聚合反應係在氮氣中,於配有螺旋磁攪拌器之22升不绣 網歷力網中進行,並在約90 rPB下搡作。所有溫S,壓力 及铺煙單《8及氫(若存在)之潇度均維持恆定,除非另有 說明° S及相對單賴之濃度偽於氣相中以製程氣體層析儀 作連鑛分析及飼入,以維持其所需濃度維持恆定。 聚合反應為在二階段中進行之批式製程,第一陏段包括 相翮單體或諸單Η在液態丙烯中之聚合反應,而第二階段 為乙烯與丙烯在氣相中之共聚合反懕。 在第一階段中,依序將下列成份飼入20Τ之壓力辑中並 在約10分缠内飼入:16升之液態丙烯,約等量之乙烯及烴 ,及含有下列姐成之催化劑系统:1)以上述製備之固《催 化劑成份(約0.15g),及2)在己烷中為10%瀟度之75nl三 乙鋁(TEAL)之混合物,及約等量之瓖己基甲基二甲氧基矽 烷(0><»(5)«子給予|9,使冉1/0>^5莫耳比例為7.5。催化劑 系铳係以丙烯加壓飼入懕力媧中。 溫度在約10分鐘内升至所需程度,並在竪僩聚合反應期 本姝Λ尺度^中S 8家楳準(CHS)甲4規格(210x297·;^)5 - 裝· 訂 線· -濟郎屮央桴準An工消ff·合作杜印rt,,4 五、發明説明(1 if)Λ 6 η G V. Description of the invention (i 3) Settling and then remove the heating body with a siphon tube, solidify at 60 ° C and wash with 200 ml parts of anhydrous hexane for 6 times, then wash at room temperature for 3 times, and dry in vacuum The post-solid has a surface porosity H5 # / g of 0.261c> c / !? and an overall density of 0.44.fi/cc. Examples 1-3 show heterogeneous olefin polymer complexes and methods for preparing the polymer. General start of polymerization The polymerization reaction is carried out in nitrogen, in a 22-liter non-embroidered wire mesh equipped with a spiral magnetic stirrer, and is operated at about 90 rPB. All temperature S, pressure and smoke laying sheet "8" and hydrogen (if present) are kept constant unless otherwise stated. ° S and relative single-layer concentration are assumed to be in the gas phase using process gas chromatograph as continuous ore Analyze and feed to maintain the required concentration constant. The polymerization reaction is a batch process carried out in two stages. The first stage includes the polymerization reaction of phase monomers or monomers in liquid propylene, while the second stage is the copolymerization reaction of ethylene and propylene in the gas phase. Sorrowful. In the first stage, the following ingredients are fed into the 20T pressure series in sequence and fed within about 10 minutes: 16 liters of liquid propylene, approximately equal amounts of ethylene and hydrocarbons, and a catalyst system containing the following sister : 1) Based on the solid catalyst prepared above (about 0.15g), and 2) a mixture of 75nl triethylaluminum (TEAL) with 10% hexane in hexane, and about the same amount of urnyl methyl di Methoxysilane (0> < »(5)« sub-giving | 9, so that Ran 1/0 > ^ 5 molar ratio is 7.5. The catalyst system is fed with propylene into the moxibustion under pressure. The temperature is at Rise to the desired level in about 10 minutes, and in the vertical polymerization period, the standard of the ^^ S 8 Jia Yu standard (CHS) A 4 specifications (210x297 ·; ^) 5-Installation · Threading ·-Jilang Laoyang桴 准 An 工 消 ff · Cooperative Du Yin rt ,, 4 V. Description of the invention (1 if)
Λ H G 經濟郎屮央榀準而Π工消仲合作社印奴 間 维 持 恆. 定 t 所 設 定 之 反 應 時 間過 後, 本 霣 上 所 有 未 反 應 之 (諸) 單 體 薄 著 在 60 V 之 大 氣 壓力 去 除 氣 體 而 濟 除 0 第 二 階 段 中 » 第 一 階 段 之 聚合 • 物 產 物 (ε 1 ) 在 樣 Si 進 行 各 種 分 析 後 t 將 其 溫 度 升 至 第 二階 段 設 之 溫 度 % 接 著 將 乙 烯 及 丙 烯 飼 入 壓 力 級 中 » 其 比例 及 量 為 可 使 達 到 所 需 之 壓 力 及 氣 相 姐 成 〇 在 聚 合 反 應 期間 9 壓 力 及 氣 相 姐 成 藉 著 飼 入 設 定 之 丙 烯 及 乙 烯 混 合 物 而維 持 » 其 m 入 像 利 用 可 調 節 或 测 量 或 兼 調 節 與 測 量 流 速 之装 置 〇 m 入 時 間 之 長 度 係 隱 著 所 用 之 催 化 劑 系 統 及 在 特 定多 相 烯 烴 聚 合 物 產 物 中 所 需 之 成 份 ( b ) 及 (G ) 之 量 而 異。 在 第 二 階 段 聚 合 反 應 終 结 時 ,加 人 粉 末 並 安 定 化 P 接 著 在 60 t: 之 氣 氣 流 烘 箱 中 乾 m 0 成 份 與 相 闞 之 搡 作 條 件 列 於 表 1 A, 且 澜 試 结 果 列 於 表 1B 〇 荞 1 A SL M. 1 2 3 第 丄 相 溫 度 * r 70 70 70 壓 力 » at η . 31 31 . 31 時 間 , 分 鐘 30 20 30 氣 相 中 之 Ηζ 1 η 耳 % 0 • 58 0 .10 0 _ 30 氣 相 中 之 乙 烯 参 U 耳 % 1 .45 2 .60 2 .50 聚 合 物 中 之 乙 烯 t Wt .% 3.0 4· 3 4 . 1 固 有 黏 度 9 d 1 / % 2 • 18 3 .0.9 2 .31 二 甲 苯 可 溶 部 份 9.4 9 . 0 10 . 7 (請先閲-背而之注-事項#塡寫本玎) 本紙張尺度»»1中《«家楳準((;肠)肀4規格(21〇><297':^)6- - 五、發明説明(15) Λ β IU5 經尔部中央標準Χ';Α工消1V-合作杜印¾ (S .) t w t • 96 二 甲 苯 中 可 溶 之 乙 烯 11 16 17 (C «) > .% — 甲 苯 中 可 溶 之 固 有 黏 度 1.15 1 39 1 . 19 (I .V d 1/ g 第 _2_ 相 溫 度 I 50 50 50 壓 力 t at ffl . 11.3 11 .5 11 .3 時 間 » 分 鏟 335 500 250 氣 相 中 之 H2 » 莫 耳 % 2.23 3 .0 2 . 05 氣 相 中 之 乙 烯 9 莫 耳 % 15.9 16 .9 22 . 54 表 1 B SL Ά. 7 2 3 昜 終 奔 物 產 生 時 K g Po 1/g Ca t 11 16 .3 9 .9 共 單 體 » W t .% 24.6 22 .7 29 .0 二 聚 物 (b ) + ( c ), t . % 70 67 71 .8 固 有 黏 度 » d 1 / g 2 .05 2 .3 2 . 34 甲 苯 溶 解 份 63.4 60 .5 63 .5 (Sr) • w t .9t 二 甲 苯 溶 解 之 乙 烯 V t . % 30 . 2 27 .0 34 .8 (Cr ) 二 甲 苯 溶 解 之 固 有 黏 度 1 . 83 2 . 02 2 . 12 I . V . s r • d l / g (請先閲1?背而之注意事項#填π本頁) 裝. 線_ 本紙5t尺度MP1中曲國家標準(CNS)甲4規格(210 X 297'iU|>7 -Λ HG Economy Lang Gyongyang is accurate and the Ingong Room of the Ugongxiaozhong Cooperative Society remains constant. After the reaction time set by t, all unreacted monomer (s) on this spot are thinned to remove gas at an atmospheric pressure of 60 V. Eliminate 0 in the second stage »The polymerization of the first stage • product (ε 1) After various analyses of the sample Si t raise its temperature to the temperature% set in the second stage and then feed ethylene and propylene into the pressure stage »The proportion and amount are such that the desired pressure and gas phase can be achieved during the polymerization reaction. 9 The pressure and gas phase are maintained by feeding the set propylene and ethylene mixture» The m image utilization can be adjusted The length of the input time or the device that measures or adjusts and measures the flow rate varies depending on the catalyst system used and the amount of components (b) and (G) required in the specific heterogeneous olefin polymer product. At the end of the second stage polymerization reaction, add powder and stabilize P. Then dry the m 0 composition and phase conditions in the airflow oven at 60 t: in Table 1A, and the test results are listed in the table. 1B buckwheat 1 A SL M. 1 2 3 Phase temperature * r 70 70 70 Pressure »at η. 31 31. 31 Time, minutes 30 20 30 Ηζ 1 η in gas phase% 0 • 58 0 .10 0 _ 30 Ethylene ginseng in gas phase% 1.45 2.60 2.50 Ethylene in polymer t Wt.% 3.0 4 · 3 4. 1 Intrinsic viscosity 9 d 1 /% 2 • 18 3 .0.9 2.31 Xylene soluble fraction 9.4 9. 0 10. 7 (please read first-back to the note-matter # 塡 写 本 玎) This paper standard »» 1 "« Jiayu quasi ((; intestine) 肀4 Specifications (21〇 < 297 ': ^) 6--V. Description of the invention (15) Λ β IU5 Central Standards of the Ministry of Economic Affairs Χ'; Α 工 消 1V-Cooperative Du Yin ¾ (S.) tw t • 96 Ethylene soluble in xylene 11 16 17 (C «) >.% — intrinsic viscosity soluble in toluene 1.15 1 39 1. 19 (I .V d 1 / g Phase _2_ phase temperature I 50 50 50 Pressure t at ffl. 11.3 11 .5 11 .3 Time »Split blade 335 500 250 H2 in gas phase» Molar% 2.23 3 .0 2. 05 Ethylene in gas phase 9 Molar% 15.9 16 .9 22. 54 Table 1 B SL Ά. 7 2 3 K g Po 1 / g Ca t 11 16 .3 9 .9 comonomer at the time of final product generation »W t.% 24.6 22 .7 29 .0 dimerization (B) + (c), t.% 70 67 71 .8 Intrinsic viscosity »d 1 / g 2 .05 2 .3 2. 34 Toluene solubility 63.4 60 .5 63 .5 (Sr) • wt .9t Ethylene dissolved in xylene V t.% 30. 2 27 .0 34 .8 (Cr) Intrinsic viscosity of dissolved xylene 1.83 2. 02 2. 12 I. V. Sr • dl / g (Please read 1 first ? Backward notes #fill this page) Pack. Thread _ this paper 5t ruler Qu MP1 National Standards (CNS) A 4 size (210 X 297'iU | > 7 -
五、發明説明(16) 皤 份 (b) ,vt.96 9.45 9.37 11.34 ϋ 份 ( c) ,vt.96 60.55 57.63 60.46 乙 烯 餾 份 (b ) , . % 51.9 57 . 1 53.7 乙 烯 餾 份 (c ) , v t , 96 31.1 27 . S 35.7 餾 份 (C)之固有黏度 1.86 2.05 2 . 18 (I .V C ). d 1 / g 熔 融 指 數 150 147 145 撓 曲 棋 數 • MPa 30 77 82 在 -5 0 υ之衝擊強度 J / HB1 HB NB 蕭 氏 D 硬 度 24 25 ^ 20 在 75¾ 之 張力% 41 28 36 張 力 強 度 ,MPa 13.8 15.8 15.4 產 生 時 之 張力強度,MPa 5 . 0 5.8 4.6 破 裂 時 之 伸長度,% 517 925 940 白 Μ > 96 31 34 35 玻 璃 轉 移 2,t: -25 (P) -23 (P) -28 (P: -75 -1 1 9 ~81 -1 28 -121 -125 装. 訂_ 線_ M濟部屮央標準i.JA工消作合作杜印¾ 1 HB =無破裂 2 (P)=主要峰 奮例4 此等實例說明多相烯烴聚合物姐合物之膜物質及其製造 方法。 本紙张尺度Wffl中B B家樣準(CNS)甲4規IM210X297公4)g - 經濟部屮央榀準·知A工消疗合作社印¾ ^ 五、發明説明(17) 以每1Q0份烯烴聚合物姐合物(PPh)為0.25份之十八综基 -3,5 -雙(1,1-二甲基乙基卜4 -羥基笨丙酸酯,〇.〇5 PPh肆 [亞甲基(3,5-二第三丁基-4-羥«氫化肉桂酸酯)]甲综’ C.OS pph Standostab P_EFQ组合物’主要成份之线( 2,4-二第三丁基笨基)_4,4'-二伸笨基二亞磷酸鼸•及 0.05pph之硬脂酸钙所穩定化之實例2之多相烯烴聚合物姐 合物之空氣驟冷吹塑膜,係》著將姐合物饋入單嫘旋擠出 器,经由圓形模具擠壓,並以足量之空氣吹塱成膜’而得 1密耳厚之膜,係使用下列設備及加工條件: 揉旋 懕縮比例3:1至4:1,麥烯烴霣 池型L/D比例:24:1至30:1,吹 塑比例:2.5至4.1;棋具間陳 :對0.5至5密耳厚度而言為 40密耳。 擠®桶輪廊: 自區1至區6為380至430 T 接受器及棋具溫度: 450 T,除了模具區W上及K下 ' 為 4 6 0 T K 外。 螺旋速度: 20 rpm ® 力: 3000 ps ί 所得膜之性霣列於下表2。 表_2 _榭版_ 性霣 實例 2 HDPE1 , LLDPE2 (請先閲lifi背而之注竞卞項洱塡寫本玨) 裝. 訂- 線· 本紙張尺度W1中a B家樣华(CNS) T 4規格(210 X 297公4)g - Λ fi W 6 經濟部屮央榀準X,IA工消"合作杜印製V. Description of the invention (16) The fraction (b), vt. 96 9.45 9.37 11.34 ϋ fraction (c), vt. 96 60.55 57.63 60.46 ethylene fraction (b),. 51.9 57. 1 53.7 ethylene fraction (c ), vt, 96 31.1 27. S 35.7 fraction (C) inherent viscosity 1.86 2.05 2. 18 (I .VC). d 1 / g melt index 150 147 145 deflection chess number • MPa 30 77 82 at -5 0 υ impact strength J / HB1 HB NB Shore D hardness 24 25 ^ 20 Tension% at 75¾ 41 28 36 Tensile strength, MPa 13.8 15.8 15.4 Tensile strength at the time of generation, MPa 5.0 0 5.8 4.6 Elongation at break ,% 517 925 940 white M > 96 31 34 35 glass transfer 2, t: -25 (P) -23 (P) -28 (P: -75 -1 1 9 ~ 81 -1 28 -121 -125 . Order _ line _ M Jibei central standard i.JA industrial and consumer cooperation Du Yin ¾ 1 HB = no crack 2 (P) = main peak Fen Example 4 These examples illustrate the film of heterogeneous olefin polymer complex Substance and its manufacturing method. This paper standard Wffl BB home sample standard (CNS) A 4 regulation IM210X297 public 4) g-Printed by the Ministry of Economic Affairs. Description (17) For every 1Q0 parts of olefin polymer compound (PPh) is 0.25 parts of eighteen-synyl-3,5-bis (1,1-dimethylethyl 4-hydroxybenzyl propionate, 〇.〇5 PPh [Methylene (3,5-di-tert-butyl-4-hydroxy «hydrocinnamic acid ester]) A comprehensive 'C.OS pph Standostab P_EFQ composition' line of main ingredients (2, 4-di-tert-butylbenzyl) _4,4'-dibenzyl diphosphite phosphite • 0.05pph calcium stearate stabilized in the air phase of the heterophasic olefin polymer compound of Example 2 Cold-blown film, "Filling the sister compound into a single-rotating extruder, extruding through a circular die, and blowing a sufficient amount of air to form a film" to obtain a 1 mil thick film, which is used The following equipment and processing conditions: Kneading and constricting ratio 3: 1 to 4: 1, wheat olefin pond type L / D ratio: 24: 1 to 30: 1, blow molding ratio: 2.5 to 4.1; between chess sets: yes It is 40 mils for a thickness of 0.5 to 5 mils. Squeeze® Bucket Contour: 380 to 430 T from Zone 1 to Zone 6 Receiver and chess tool temperature: 450 T, except that the mold zone W up and K down is 4 6 0 T K. Spiral speed: 20 rpm ® Force: 3000 ps ί The properties of the resulting film are listed in Table 2 below. Table_2 _ 赛 版 _ Examples of Sex Encyclopedia 2 HDPE1, LLDPE2 (please read the note on the back of the lifi first, the Bian Xiang Er 塡 縨 玨) installed. Order-line · this paper standard W1 a B home sample (CNS) T 4 Specifications (210 X 297 gong 4) g-Λ fi W 6 Ministry of Economic Affairs 汮 央 榀 X, IA 工 消 " cooperative printing
、發明説明 (ιδ) 產生強度. 1347/1126 3757/3145 1749/1739 (HD/CD3) .p s i 破裂強度 3095/1643 3960/3216 2092/1898 (M D / C D ). p s i 產生時伸 長度 65/40 30/7 80/17 (MD/CD), 96 破裂時伸 長度 361/417 120/350 317/425 (MD/CD), % Ε 1 e a e n d 〇 rf撕裂 No tear 10/282 350/790 (MD/CD), g / p 1 y Trouser 撕裂 152/530 147/1026 503/758 (HD/CD) 白辖 65.7 76 . 8 8.7 光澤度 6 10 70 摩擦係數 (靜摩1 .22/0.815 0.241/0.192 0.688/0.650 擦/動摩擦) 在100°F及100相 1.340 1.300 - 對溼度下 之溼蒸 氣穿透, g/ 100 s q , in/24 h r s. 挪針衡擊 強度 0.980 0.720 1 . 020 ft-lb/密耳 1 .具有0. 9 5 3 g / cc 3密度之Qua ntun L R 7 3 2, HDPE 2 .含己烯-1 且具有 Ο . 9 2 0 g / cc 3 密度之 D o w 1 e x 2 Ο 4 5 L L D P E (-先間-背而之注*卞項洱堝"本玎) 本紙張尺度MW中《國家樣準(CNS) Ή規IM210X297公雀沁- 21·^ 五、發明説明(1 S ) Λ 6 Π 6 3. MD/CD =櫬械方向/交錯方向。 由上表可看出,本發明之烯烴聚合物姐合物可提供在破 裂時具有改鸟伸長度及Elesendsrf撕裂性質及較佳平衡性 質之空氣费冷吹塑膜。再者,包括丙烯單元:Z主要部份之 聚合物物質通常無法在空氣驟冷吹塑膜設備中充分進行。 此實例 烯烴聚合 ,及其製 以上述 製備,係 ,並於冷 用下列設 螈旋設計 懕縮比 飼入區 說明多相烯烴聚合物姐合物之澆鑄膜物質,多相 物姐合物之共擠出膜及丙烯及乙烯之無規共聚物 造方法。 實例4安定化之霣例2之多相烯烴聚合物$合物之 利用將姐合物饑入擠臛櫬中,經由平膜横具擠出 凍滾茼上驟冷*以產生1密耳厚之膜*擠壓係使 備及加工條件: 例: 4 : 1 至 3 : 1 深度: 0.435至0.490"(具有3.5: 1®縮比例 之3 . 5〃擠壓機), 量測區深度: 3.5〃擠壓機而言為0.125至0.140〃 般中心飼入掛跔岐管 (請先閲背而之注意卞項洱填艿木狂) 裝. 訂 線· 經濟部屮央榀準而β工消作合作杜印3i 横具:一 擠懕機搡 熔融溫 擠壓機 接受器 1 . 25 密 作條件: 度: 430 -500 Τ 屏陣: 自區1至區6為350 -420 Τ 及横具溫度:420 Τ 耳厚之共擠壓膜包括作為中心層之上述實例4安 本紙5fc尺度W1中困國家楳準(CNS) T4規怙(210X297公- 2 V扣 ο :· ^ g 五、發明説明(20) 定化之»例2之多相烯烴聚合物組合物之膜層,及具有乙 烯含量為3.0%之Pro-fax SA 861丙烯-乙烯無規共聚物之 二層膜屐·以並澆鐮麟枝術製備中心層之各表面上之該共 聚物層 所得膜之性質列於下表3。 性質 表 3 榭胞 實例2 C o e X 1 P - E Co2 產生強度 1185/865 1095/817 2523/2452 (MD/CD3) ,PS i 破裂強度 3899/1708 3637/1693 4120/3363 (MD/CD), P s i 產生時之 伸長 度 34/19 32/22 15/10 (MD/CD). % 跛裂時之 伸長 度 450/550 530/550 522/584 (HD/CD). % E1e *e n do 「f撕裂性192/No 657/544 49/102 (MD/CD), g / P ly Tear 白霧 49.0 5.2 2.3 光澤度 20.0 57.0 78.1 1.丙烯-乙烯無規共聚物/實例 2之多相烯烴 聚合物姐合 /丙烯- 乙烯 無規 共聚物。 , 2 .具乙烯 含量 為3 . 0% 之 P「o'f ax 861丙嫌- 乙烯無規共 經濟部屮央榀準杓员工消价合作杜印製 (請先閲-背而之注总事項#填"本玎) 本紙張尺度_中8»家樣準(35)〒4規岱(210>:297公_电)2-3. Description of the invention (ιδ) strength. 1347/1126 3757/3145 1749/1739 (HD / CD3). Psi burst strength 3095/1643 3960/3216 2092/1898 (MD / CD). Elongation at psi 65/40 30/7 80/17 (MD / CD), 96 Elongation at break 361/417 120/350 317/425 (MD / CD),% Ε 1 eaend 〇rf tear No tear 10/282 350/790 (MD / CD), g / p 1 y Trouser tear 152/530 147/1026 503/758 (HD / CD) Baiju 65.7 76. 8 8.7 gloss 6 10 70 coefficient of friction (static friction 1.22 / 0.815 0.241 / 0.192 0.688 / 0.650 rub / dynamic friction) at 100 ° F and 100 phases 1.340 1.300-penetration of wet vapor under humidity, g / 100 sq, in / 24 hr s. Moving needle balance strength 0.980 0.720 1 .020 ft- lb / mil 1. Quattun LR 7 3 2, HDPE 2 with density of 0.95 3 g / cc 3 HDPE 2. D ow 1 ex with hexene-1 and density of 0.92 0 g / cc 3 2 Ο 4 5 LLDPE (-first time-backward note * Bian item Erguo " 本 玎) This paper scale MW "National Sample Standard (CNS) Ή regulation IM210X297 Gongqueqin-21 · ^ V. Description of invention (1 S) Λ 6 Π 6 3. MD / CD = machine direction / interlaced direction. As can be seen from the above table, the olefin polymer compound of the present invention can provide an air-fed cold blown film with improved bird elongation and Elesendsrf tearing properties and better balance properties when broken. Furthermore, the polymer material including the main part of propylene unit: Z usually cannot be sufficiently carried out in the air quench blown film equipment. The olefin polymerization of this example, and its preparation are based on the above-mentioned preparation, and in the cold setting of the following design of the curling ratio feed zone to illustrate the casting film material of the heterogeneous olefin polymer compound and the heterogeneous compound compound Co-extrusion film and random copolymer production method of propylene and ethylene. Example 4 Utilization of the stable heterophasic olefin polymer compound Example 2 The sister compound was hungry into a squeeze, extruded through a flat film crosspiece and quenched on a frozen roller to produce 1 mil thickness Film * Extrusion system preparation and processing conditions: Example: 4: 1 to 3: 1 Depth: 0.435 to 0.490 " (with 3.5: 1® reduction ratio of 3.5mm extruder), measuring area depth : For the 3.5〃extruder, it is 0.125 to 0.140〃. The center feeds the hanging manifold (please read the back first and pay attention to Bian Xianger to fill the wood fan). Threading · Ministry of Economic Affairs Cooperate with Duyin 3i horizontal bar: a squeeze machine and melt temperature extruder receiver 1. 25 dense working conditions: degree: 430 -500 Τ screen array: from zone 1 to zone 6 is 350 -420 ton and cross bar Temperature: 420 ton thick co-extruded film including the above example as the central layer 4 Aberdeen paper 5fc scale W1 in troubled countries (CNS) T4 regulations (210X297 male-2 V buckle: · ^ g V. Invention Description (20) The film layer of the heterogeneous olefin polymer composition of Example 2 and the two-layer film of Pro-fax SA 861 propylene-ethylene random copolymer with an ethylene content of 3.0%. The properties of the film obtained by pouring the copolymer layer on each surface of the central layer by pouring the sickle are listed in the following Table 3. Properties Table 3 Cell Example 2 C oe X 1 P -E Co2 Yield strength 1185/865 1095/817 2523/2452 (MD / CD3), PS i Bursting strength 3899/1708 3637/1693 4120/3363 (MD / CD), P si elongation 34/19 32/22 15/10 (MD / CD). % Elongation during lameness 450/550 530/550 522/584 (HD / CD).% E1e * en do 「f tearability 192 / No 657/544 49/102 (MD / CD), g / P ly Tear white fog 49.0 5.2 2.3 gloss 20.0 57.0 78.1 1. Propylene-ethylene random copolymer / heterogeneous olefin polymer of Example 2 / propylene-ethylene random copolymer., 2. Has an ethylene content of 3. 0% of P "o'f ax 861 Propane-Ethylene Random Communist Ministry of Economics and Social Development Employee Price Bargaining Cooperative Printing (Please read-Back-to-Note Note Total Matters #Fill in &#; 本 玎) Paper Scale_Zhong 8 »Home Sample Standard (35) 〒4 gauge Dai (210 >: 297 gong_electricity) 2-
Λ 6 Π G 五、發明説明(21) 物。 3. MD/CD =檐械方向/交錯方向 由上表可看出木發明之烯烴聚合物姐合钧可提供具有在 產生時之改良伸長性及EUEendorf撕裂性質之澆鳙膜及共 旖出澆鏑賴。 習知厚度之各種型之膜物質及小於20密耳厚及薄如約 0.5密耳厚之薄膜可使用本文所述之多相烯烴聚合物姐合 物及重縝物霣,一般表示為20至100密耳厚之片狀物而製 備•例如•其可用Μ製備澆鑄膜·未軸向及雙軸定向臢* 及擠壓片或砑光片,此外,包括多相烯烴聚合物辑合物之 贗可利用積暦或共擠颸技術而施用至熱塑性R物質•或金 雇片或萡片之至少一表面上。一般熱塑性物爾包含C2-1〇 α -烯烴單雅之结晶均聚物,如丙烯或乙烯,或丙烯與乙 烯或輿Cmct-烯烴單體之共聚物*或丙烯與乙烯及 C4-10 ct -烯烴單《之共聚物,但當單《為乙烯時,最大 聚合之乙烯含量為約10%,較好約4%,且當共單體為 Cm烯烴時,其最大之聚合含ft為約20% ·較好約16% •且當同時使用乙烯及cc -烯烴時,兩者之最大聚合含量 為30% ·較好為20% :及包含聚酯,聚》胺,乙烯-乙烯 酵共聚物及乙烯-醏酸乙烯酯共聚物;鋁為通宜之金牖基 材。 此外膜物質可由約5至45%之本文所述之多相烯烴聚合 物共聚物及約95至55%之C2-1〇a -烯煙單輝之结晶均聚物 或丙烯與乙烯或與C4-1〇a-烯烴單《之共聚物,或丙烯, 本《張尺度細中ΒΒ家《準(CNS)>f4規格(210X297公处)3- 裝. 訂- 線·Λ 6 Π G 5. Description of the invention (21). 3. MD / CD = eaves machine direction / staggered direction. As can be seen from the table above, the olefin polymer Sister Hejun of the wood invention can provide a cast bighead film with improved elongation and EUEendorf tearing properties and co-extraction during production. Dysprosium. Various types of film materials of conventional thickness and films less than 20 mils thick and as thin as about 0.5 mils thick can use the heterophasic olefin polymer complexes and heavy objects described herein, generally expressed as 20 to 100 mil thick sheets are prepared • For example • It can be used to prepare cast films • Unaxial and biaxially oriented sheets * and extruded sheets or calendered sheets, in addition, including heterogeneous olefin polymer compounds Pseudomass can be applied to at least one surface of thermoplastic R substance • or Jinxun tablets or sepals using accumulator or co-extrusion technology. General thermoplastics include crystalline homopolymers of C2-1〇α-olefins, such as propylene or ethylene, or copolymers of propylene and ethylene or Cmct-olefin monomers * or propylene and ethylene and C4-10 ct-olefins The copolymer of single ", but when the single" is ethylene, the maximum polymerized ethylene content is about 10%, preferably about 4%, and when the comonomer is Cm olefin, the maximum polymerization content of ft is about 20% · Preferably about 16% • And when both ethylene and cc-olefin are used, the maximum polymerization content of the two is 30% • Preferably 20%: and contains polyester, poly》 amine, ethylene-vinyl yeast copolymer and Ethylene-vinyl acetate copolymer; aluminum is Tongyi's base material. In addition, the membrane material may be composed of about 5 to 45% of the heterophasic olefin polymer copolymer described herein and about 95 to 55% of C2-1〇a-ene smoke mono-hui crystalline homopolymer or propylene and ethylene or C4- 1〇a-olefin single "copolymer, or propylene, this" Zhang scale detailed BB home "(CNS)> f4 specifications (210X297 public office) 3- Pack. Binding-line ·
Λ fi 15 G 五、發明説明(22) 乙 及 C 4 _ 1 〇 -烯烴單《之共聚物之接合物而製備。該共 聚物具有乙烯,或CI -烯烴或兩者之最大聚合含量述於下 段,较好於此種摻合物中存在之多相烯烴聚合物姐合资之 量為1 0至3 0 % ·- 本發明之烯烴聚合物姐合物為當相同之膜曆物質腌用至 其他熱塑性物霣之至少一面,或金羼性基材上時,可使所 得產物之性質得良好平衡者*且當其與其他熱塑性物霣摻 合時*摻合物可用以製成膜物質。 本文所掲示之本發明之其他持激·優點及具體例在詳讀 前述揭示時•將使熟悉本技藝者更易於了解;Μ»此黏, 本發明之特定具體例已更詳佃敘述,此等具«例之改變及 修飾可在不違背本發明申請之精神及範麵内進行。 (請先閲1.?背而之;.£*卞項#填寫本1®) Γ % 經濟部屮央捣準凡A工消伢合作社印3i 本紙5t尺度中國明¥:楳準(CNS)甲4規格(210 X 297公与)4 -Λ fi 15 G V. Description of the invention (22) The preparation of a conjugate of a copolymer of B and C 4 — 1 〇-olefin monomer. The copolymer has a maximum polymerization content of ethylene, or CI-olefin or both, as described in the next paragraph, preferably the amount of the multiphase olefin polymer joint venture present in this blend is 10 to 30% ·- The olefin polymer compound of the present invention is that when the same film calendar material is applied to at least one side of other thermoplastics, or on a gold substrate, the properties of the resulting product can be well balanced * and when it is When blended with other thermoplastics, the blend can be used to make film materials. Other motivations, advantages, and specific examples of the present invention shown in this article will make it easier for those familiar with the art to understand when reading the foregoing disclosure; Μ »This is sticky, and specific specific examples of the present invention have been described in more detail. Changes and modifications such as examples can be made without departing from the spirit and scope of the present application. (Please read 1.? Backwards ;. £ * 卞 项 #Fill in this 1®) Γ% The Ministry of Economic Affairs of the People ’s Republic of China stamped the Fan A Industrial Consumers Cooperative Society printed 3i this paper 5t scale China Ming: ¥ 揳 准 (CNS) A 4 specifications (210 X 297 gong) 4-
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| Application Number | Priority Date | Filing Date | Title |
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| US74905590A | 1990-08-27 | 1990-08-27 | |
| US58985790A | 1990-09-28 | 1990-09-28 |
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| TW213934B true TW213934B (en) | 1993-10-01 |
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