TW201008963A - Modified polyolefins - Google Patents
Modified polyolefins Download PDFInfo
- Publication number
- TW201008963A TW201008963A TW098122709A TW98122709A TW201008963A TW 201008963 A TW201008963 A TW 201008963A TW 098122709 A TW098122709 A TW 098122709A TW 98122709 A TW98122709 A TW 98122709A TW 201008963 A TW201008963 A TW 201008963A
- Authority
- TW
- Taiwan
- Prior art keywords
- group
- polyolefin
- polymer
- decane
- unsaturated
- Prior art date
Links
- 229920000098 polyolefin Polymers 0.000 title claims abstract description 109
- 238000000034 method Methods 0.000 claims abstract description 84
- 238000006243 chemical reaction Methods 0.000 claims abstract description 30
- 150000003254 radicals Chemical class 0.000 claims abstract description 30
- 239000000945 filler Substances 0.000 claims abstract description 28
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 22
- 239000002131 composite material Substances 0.000 claims abstract description 18
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000005977 Ethylene Substances 0.000 claims abstract description 14
- 230000000694 effects Effects 0.000 claims abstract description 14
- 230000008569 process Effects 0.000 claims abstract description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000001257 hydrogen Substances 0.000 claims abstract description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 8
- 229920006112 polar polymer Polymers 0.000 claims abstract description 4
- 230000004913 activation Effects 0.000 claims abstract description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 2
- -1 polypropylene Polymers 0.000 claims description 172
- 239000004743 Polypropylene Substances 0.000 claims description 133
- 229920001155 polypropylene Polymers 0.000 claims description 132
- 229920000642 polymer Polymers 0.000 claims description 80
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 78
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 73
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical class CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 claims description 69
- 239000000203 mixture Substances 0.000 claims description 62
- 239000003054 catalyst Substances 0.000 claims description 55
- 150000001875 compounds Chemical class 0.000 claims description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
- 229920000578 graft copolymer Polymers 0.000 claims description 31
- 238000004132 cross linking Methods 0.000 claims description 30
- 230000015556 catabolic process Effects 0.000 claims description 29
- 238000006731 degradation reaction Methods 0.000 claims description 29
- 238000009833 condensation Methods 0.000 claims description 28
- 230000005494 condensation Effects 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 14
- 150000002430 hydrocarbons Chemical group 0.000 claims description 12
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 12
- 238000010894 electron beam technology Methods 0.000 claims description 9
- 239000004575 stone Substances 0.000 claims description 9
- 238000005520 cutting process Methods 0.000 claims description 8
- OZZYKXXGCOLLLO-TWTPFVCWSA-N ethyl (2e,4e)-hexa-2,4-dienoate Chemical group CCOC(=O)\C=C\C=C\C OZZYKXXGCOLLLO-TWTPFVCWSA-N 0.000 claims description 8
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 8
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 239000000049 pigment Substances 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 238000011065 in-situ storage Methods 0.000 claims description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 4
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical group OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- 150000001336 alkenes Chemical group 0.000 claims description 4
- 238000000576 coating method Methods 0.000 claims description 4
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 4
- 229910052707 ruthenium Inorganic materials 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 239000000779 smoke Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 claims description 2
- 239000000976 ink Substances 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000002429 hydrazines Chemical class 0.000 claims 5
- 230000003213 activating effect Effects 0.000 claims 3
- QTDAXPXRSUIMFH-UHFFFAOYSA-N 1,1,1,2-tetramethoxydecane Chemical compound COC(C(OC)(OC)OC)CCCCCCCC QTDAXPXRSUIMFH-UHFFFAOYSA-N 0.000 claims 1
- YWLHMCYTOSAPCI-UHFFFAOYSA-N C(C(=C)C)(=O)OC(C(OC)(OC)OC)CCCCCCCC Chemical compound C(C(=C)C)(=O)OC(C(OC)(OC)OC)CCCCCCCC YWLHMCYTOSAPCI-UHFFFAOYSA-N 0.000 claims 1
- 125000000468 ketone group Chemical group 0.000 claims 1
- 239000004922 lacquer Substances 0.000 claims 1
- 238000012667 polymer degradation Methods 0.000 abstract description 11
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 abstract description 5
- 230000000704 physical effect Effects 0.000 abstract description 3
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 abstract description 2
- 150000004756 silanes Chemical class 0.000 abstract 4
- 238000012668 chain scission Methods 0.000 abstract 1
- 239000000413 hydrolysate Substances 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 71
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 30
- 239000007822 coupling agent Substances 0.000 description 22
- 238000002156 mixing Methods 0.000 description 21
- 238000010521 absorption reaction Methods 0.000 description 20
- 150000002978 peroxides Chemical class 0.000 description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 239000003153 chemical reaction reagent Substances 0.000 description 15
- 239000002253 acid Substances 0.000 description 14
- 239000000835 fiber Substances 0.000 description 14
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 13
- 239000002023 wood Substances 0.000 description 13
- 229920001112 grafted polyolefin Polymers 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- 239000003963 antioxidant agent Substances 0.000 description 11
- 229920000573 polyethylene Polymers 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 9
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- 239000000463 material Substances 0.000 description 9
- 229920005629 polypropylene homopolymer Polymers 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 239000004594 Masterbatch (MB) Substances 0.000 description 8
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 8
- 230000003078 antioxidant effect Effects 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 230000008878 coupling Effects 0.000 description 8
- 238000010168 coupling process Methods 0.000 description 8
- 238000005859 coupling reaction Methods 0.000 description 8
- 239000003365 glass fiber Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 7
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 7
- 239000002671 adjuvant Substances 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 7
- 235000013312 flour Nutrition 0.000 description 7
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- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 6
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 6
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
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- 150000003839 salts Chemical class 0.000 description 6
- 239000000565 sealant Substances 0.000 description 6
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 5
- JZHKIUBMQMDQRG-UHFFFAOYSA-N C(=C)C(C(OC)(OC)OC)CCCCCCCC Chemical compound C(=C)C(C(OC)(OC)OC)CCCCCCCC JZHKIUBMQMDQRG-UHFFFAOYSA-N 0.000 description 5
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- 239000000052 vinegar Substances 0.000 description 5
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- CWZQYRJRRHYJOI-UHFFFAOYSA-N 1,1,1-trimethoxydecane Chemical compound CCCCCCCCCC(OC)(OC)OC CWZQYRJRRHYJOI-UHFFFAOYSA-N 0.000 description 4
- OAWZPHCPLADLAD-UHFFFAOYSA-N 4-(trimethoxymethyl)dodecyl prop-2-enoate Chemical compound C(C=C)(=O)OCCCC(C(OC)(OC)OC)CCCCCCCC OAWZPHCPLADLAD-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
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- 238000003776 cleavage reaction Methods 0.000 description 4
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 4
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- DBJFSFSBHGPDPG-UHFFFAOYSA-N C(C(=C)C)(=O)OCCCC(C(OC)(OC)OC)CCCCCCCC Chemical group C(C(=C)C)(=O)OCCCC(C(OC)(OC)OC)CCCCCCCC DBJFSFSBHGPDPG-UHFFFAOYSA-N 0.000 description 3
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- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical compound OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000010454 slate Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229940075554 sorbate Drugs 0.000 description 1
- 108010004034 stable plasma protein solution Proteins 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 159000000008 strontium salts Chemical class 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
- 239000003451 thiazide diuretic agent Substances 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N trans-Stilbene Natural products C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- LSZKGNJKKQYFLR-UHFFFAOYSA-J tri(butanoyloxy)stannyl butanoate Chemical compound [Sn+4].CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O.CCCC([O-])=O LSZKGNJKKQYFLR-UHFFFAOYSA-J 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- CPRPKIMXLHBUGA-UHFFFAOYSA-N triethyltin Chemical compound CC[Sn](CC)CC CPRPKIMXLHBUGA-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 239000011155 wood-plastic composite Substances 0.000 description 1
- 229940075420 xanthine Drugs 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/08—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having four or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/06—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J151/00—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers
- C09J151/06—Adhesives based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Adhesives based on derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0812186.5A GB0812186D0 (en) | 2008-07-03 | 2008-07-03 | Modified polyolefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW201008963A true TW201008963A (en) | 2010-03-01 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW098122709A TW201008963A (en) | 2008-07-03 | 2009-07-03 | Modified polyolefins |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US8569417B2 (enExample) |
| EP (1) | EP2294100B1 (enExample) |
| JP (1) | JP5580817B2 (enExample) |
| KR (1) | KR101603083B1 (enExample) |
| CN (1) | CN102076725B (enExample) |
| BR (1) | BRPI0913931A2 (enExample) |
| CA (1) | CA2729887A1 (enExample) |
| GB (1) | GB0812186D0 (enExample) |
| MX (1) | MX2010013753A (enExample) |
| RU (1) | RU2496797C2 (enExample) |
| TW (1) | TW201008963A (enExample) |
| UA (1) | UA105638C2 (enExample) |
| WO (1) | WO2010000478A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8907108B2 (en) | 2012-10-26 | 2014-12-09 | Industrial Technology Research Institute | P-type organic semiconductor material and optoelectronic device utilizing the same |
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| GB0812185D0 (en) * | 2008-07-03 | 2008-08-13 | Dow Corning | Polymers modified by silanes |
| GB201000117D0 (en) | 2010-01-06 | 2010-02-17 | Dow Corning | Organopolysiloxanes containing an unsaturated group |
| GB201000116D0 (en) | 2010-01-06 | 2010-02-17 | Dow Corning | Polyolefins modified by silicones |
| GB201000121D0 (en) * | 2010-01-06 | 2010-02-17 | Dow Corning | Modified polyolefins |
| GB201000120D0 (en) | 2010-01-06 | 2010-02-17 | Dow Corning | Process for forming crosslinked and branched polymers |
| FR2957017B1 (fr) * | 2010-03-03 | 2012-03-30 | Setup Performance | Procede de fabrication de granules de polypropylene post reticulable apres transformation ; granules obtenus et articles moules fabriques a partir des granules |
| WO2012059529A1 (en) | 2010-11-03 | 2012-05-10 | Dow Corning Corporation | Epoxidised elastomer compositions modified by silanes |
| BR112013018574A2 (pt) | 2011-01-19 | 2016-09-27 | Dow Corning | método para produção de poliolefinas funcionalizadas por silila e poliolefinas funcionalizadas por silila com incorporação de monômero de silila |
| FR2972193B1 (fr) | 2011-03-04 | 2014-07-04 | Setup Performance | Polyolefines modifiees, reticulables apres transformation, et procede de fabrication desdites polyolefines |
| US8580886B2 (en) | 2011-09-20 | 2013-11-12 | Dow Corning Corporation | Method for the preparation and use of bis (alkoxysilylorgano)-dicarboxylates |
| US9681939B2 (en) | 2011-11-18 | 2017-06-20 | Cook Medical Technologies Llc | Silane bonded medical devices and method of making same |
| EP2785726B1 (en) | 2011-12-02 | 2018-08-01 | Dow Silicones Corporation | Ester-functional silanes and the preparation and use thereof; and use of iminium compounds as phase transfer catalysts |
| GB201121133D0 (en) | 2011-12-08 | 2012-01-18 | Dow Corning | Hydrolysable silanes |
| GB201121127D0 (en) | 2011-12-08 | 2012-01-18 | Dow Corning | Treatment of filler with silane |
| GB201121128D0 (en) | 2011-12-08 | 2012-01-18 | Dow Corning | Treatment of filler with silane |
| GB201121124D0 (en) | 2011-12-08 | 2012-01-18 | Dow Corning | Hydrolysable silanes |
| GB201121122D0 (en) | 2011-12-08 | 2012-01-18 | Dow Corning | Hydrolysable silanes and elastomer compositions containing them |
| US9260556B2 (en) * | 2012-02-10 | 2016-02-16 | Mitsui Chemicals Tohcello, Inc. | Encapsulating material for solar cell and solar cell module |
| BR112017002210B1 (pt) * | 2014-08-15 | 2022-05-03 | Dow Global Technologies Llc | Espuma de polietileno enxertado com polidimetilsiloxano e método para preparar uma espuma |
| US20170283566A1 (en) | 2014-09-18 | 2017-10-05 | Borealis Ag | Film with moderate crosslinking |
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| US20190001625A1 (en) * | 2015-12-22 | 2019-01-03 | Padanaplast S.R.L. | Multilayer assembly including a composite material |
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| CN106084136A (zh) * | 2016-06-15 | 2016-11-09 | 潘海云 | 一种改性聚丙烯塑料管材及其制备方法 |
| CN106632864A (zh) * | 2016-12-05 | 2017-05-10 | 彭州市运达知识产权服务有限公司 | 一种hdpe多单体接枝聚合物及其制备方法 |
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| GB201711712D0 (en) * | 2017-07-20 | 2017-09-06 | Dow Corning | Polyamide blends |
| WO2019023008A1 (en) | 2017-07-25 | 2019-01-31 | Dow Silicones Corporation | PROCESS FOR THE PREPARATION OF A GRAFT COPOLYMER HAVING A POLYOLEFIN SKELETON AND POLYORGANOSILOXANE PENDANT GROUPS |
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| US10919989B2 (en) * | 2017-10-20 | 2021-02-16 | Iowa State University Research Foundation, Inc. | End group functionalization agents for polydiene |
| EP3768793B1 (en) | 2018-03-19 | 2023-09-27 | Dow Silicones Corporation | Polyorganosiloxane hot melt adhesive compositions containing polyolefin - polydiorganoosiloxane copolymers and methods for the preparation and use thereof |
| US11193051B2 (en) | 2018-03-19 | 2021-12-07 | Dow Silicones Corporation | Hot melt adhesive composition containing a polyolefin-polydiorganosiloxane copolymer and methods for the preparation and use thereof |
| WO2019182720A1 (en) | 2018-03-19 | 2019-09-26 | Dow Silicones Corporation | Polyolefin-polydiorganosiioxane block copolymer and method for the synthesis thereof |
| EP3768765B1 (en) | 2018-03-19 | 2023-05-17 | Dow Silicones Corporation | Polyolefin-polydiorganosiloxane block copolymer and hydrosilylaton reaction method for the synthesis thereof |
| WO2020018159A1 (en) | 2018-07-17 | 2020-01-23 | Dow Silicones Corporation | Polysiloxane resin - polyolefin copolymer and methods for the preparation and use thereof |
| CN109251270A (zh) * | 2018-08-11 | 2019-01-22 | 洛阳和梦科技有限公司 | 顺酐接枝聚丙烯的制备方法 |
| CN111100248B (zh) * | 2018-10-25 | 2022-10-11 | 中国石油化工股份有限公司 | 化学接枝型防尘棚膜用改性聚烯烃材料及其制备方法和防尘棚膜 |
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-
2008
- 2008-07-03 GB GBGB0812186.5A patent/GB0812186D0/en not_active Ceased
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2009
- 2009-07-02 EP EP09772178.1A patent/EP2294100B1/en active Active
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- 2009-07-02 MX MX2010013753A patent/MX2010013753A/es unknown
- 2009-07-02 BR BRPI0913931A patent/BRPI0913931A2/pt not_active IP Right Cessation
- 2009-07-02 JP JP2011515241A patent/JP5580817B2/ja active Active
- 2009-07-02 UA UAA201101188A patent/UA105638C2/uk unknown
- 2009-07-02 CA CA2729887A patent/CA2729887A1/en not_active Abandoned
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- 2009-07-02 CN CN2009801249926A patent/CN102076725B/zh active Active
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8907108B2 (en) | 2012-10-26 | 2014-12-09 | Industrial Technology Research Institute | P-type organic semiconductor material and optoelectronic device utilizing the same |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20110041443A (ko) | 2011-04-21 |
| BRPI0913931A2 (pt) | 2015-10-20 |
| EP2294100A1 (en) | 2011-03-16 |
| CN102076725B (zh) | 2013-08-21 |
| US8569417B2 (en) | 2013-10-29 |
| JP2011526312A (ja) | 2011-10-06 |
| JP5580817B2 (ja) | 2014-08-27 |
| MX2010013753A (es) | 2011-03-29 |
| KR101603083B1 (ko) | 2016-03-14 |
| EP2294100B1 (en) | 2018-09-12 |
| CA2729887A1 (en) | 2010-01-07 |
| WO2010000478A1 (en) | 2010-01-07 |
| US20110190411A1 (en) | 2011-08-04 |
| UA105638C2 (uk) | 2014-06-10 |
| RU2011103785A (ru) | 2012-08-10 |
| RU2496797C2 (ru) | 2013-10-27 |
| GB0812186D0 (en) | 2008-08-13 |
| CN102076725A (zh) | 2011-05-25 |
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