JP6138272B2 - 環状ケトンペルオキシドを含むマスターバッチ - Google Patents
環状ケトンペルオキシドを含むマスターバッチ Download PDFInfo
- Publication number
- JP6138272B2 JP6138272B2 JP2015545753A JP2015545753A JP6138272B2 JP 6138272 B2 JP6138272 B2 JP 6138272B2 JP 2015545753 A JP2015545753 A JP 2015545753A JP 2015545753 A JP2015545753 A JP 2015545753A JP 6138272 B2 JP6138272 B2 JP 6138272B2
- Authority
- JP
- Japan
- Prior art keywords
- masterbatch
- polymer matrix
- cyclic ketone
- vol
- ketone peroxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- -1 cyclic ketone peroxide Chemical class 0.000 title claims description 51
- 239000004594 Masterbatch (MB) Substances 0.000 title claims description 39
- 229920000642 polymer Polymers 0.000 claims description 41
- 239000011159 matrix material Substances 0.000 claims description 31
- 150000002978 peroxides Chemical class 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 20
- 239000013638 trimer Substances 0.000 claims description 19
- 239000004743 Polypropylene Substances 0.000 claims description 12
- 238000009472 formulation Methods 0.000 claims description 12
- 229920001155 polypropylene Polymers 0.000 claims description 12
- 239000002904 solvent Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000000539 dimer Substances 0.000 claims description 8
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 6
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 150000002432 hydroperoxides Chemical class 0.000 claims description 3
- 238000012986 modification Methods 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
- 239000005977 Ethylene Substances 0.000 claims 1
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims 1
- 238000005336 cracking Methods 0.000 claims 1
- 238000004132 cross linking Methods 0.000 claims 1
- 239000005038 ethylene vinyl acetate Substances 0.000 claims 1
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims 1
- 229920005606 polypropylene copolymer Polymers 0.000 claims 1
- 229920005629 polypropylene homopolymer Polymers 0.000 claims 1
- 239000000463 material Substances 0.000 description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 9
- 239000012188 paraffin wax Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 7
- 150000002576 ketones Chemical class 0.000 description 6
- 239000002360 explosive Substances 0.000 description 5
- 229920000098 polyolefin Polymers 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 238000002459 porosimetry Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- BGHCVCJVXZWKCC-UHFFFAOYSA-N tetradecane Chemical compound CCCCCCCCCCCCCC BGHCVCJVXZWKCC-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- 229920001222 biopolymer Polymers 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 150000001451 organic peroxides Chemical class 0.000 description 3
- 229920002961 polybutylene succinate Polymers 0.000 description 3
- 239000004631 polybutylene succinate Substances 0.000 description 3
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 2
- POSWICCRDBKBMH-UHFFFAOYSA-N 3,3,5-trimethylcyclohexan-1-one Chemical compound CC1CC(=O)CC(C)(C)C1 POSWICCRDBKBMH-UHFFFAOYSA-N 0.000 description 2
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- FFWSICBKRCICMR-UHFFFAOYSA-N 5-methyl-2-hexanone Chemical compound CC(C)CCC(C)=O FFWSICBKRCICMR-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229920000331 Polyhydroxybutyrate Polymers 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 235000011089 carbon dioxide Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 2
- ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012669 liquid formulation Substances 0.000 description 2
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 239000005015 poly(hydroxybutyrate) Substances 0.000 description 2
- 229920000218 poly(hydroxyvalerate) Polymers 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 229920002792 polyhydroxyhexanoate Polymers 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000007655 standard test method Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 2
- DMWVYCCGCQPJEA-UHFFFAOYSA-N 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane Chemical compound CC(C)(C)OOC(C)(C)CCC(C)(C)OOC(C)(C)C DMWVYCCGCQPJEA-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N 2-Oxohexane Chemical compound CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- FIYMNUNPPYABMU-UHFFFAOYSA-N 2-benzyl-5-chloro-1h-indole Chemical compound C=1C2=CC(Cl)=CC=C2NC=1CC1=CC=CC=C1 FIYMNUNPPYABMU-UHFFFAOYSA-N 0.000 description 1
- MIRQGKQPLPBZQM-UHFFFAOYSA-N 2-hydroperoxy-2,4,4-trimethylpentane Chemical compound CC(C)(C)CC(C)(C)OO MIRQGKQPLPBZQM-UHFFFAOYSA-N 0.000 description 1
- JJRDRFZYKKFYMO-UHFFFAOYSA-N 2-methyl-2-(2-methylbutan-2-ylperoxy)butane Chemical compound CCC(C)(C)OOC(C)(C)CC JJRDRFZYKKFYMO-UHFFFAOYSA-N 0.000 description 1
- LFSAPCRASZRSKS-UHFFFAOYSA-N 2-methylcyclohexan-1-one Chemical compound CC1CCCCC1=O LFSAPCRASZRSKS-UHFFFAOYSA-N 0.000 description 1
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 1
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 1
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 239000006001 Methyl nonyl ketone Substances 0.000 description 1
- 102000014160 PTEN Phosphohydrolase Human genes 0.000 description 1
- 108010011536 PTEN Phosphohydrolase Proteins 0.000 description 1
- KMPQYAYAQWNLME-UHFFFAOYSA-N Undecanal Natural products CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000002288 cocrystallisation Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
- 238000002307 isotope ratio mass spectrometry Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000005014 poly(hydroxyalkanoate) Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/36—After-treatment
- C08J9/40—Impregnation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/22—Compounding polymers with additives, e.g. colouring using masterbatch techniques
- C08J3/226—Compounding polymers with additives, e.g. colouring using masterbatch techniques using a polymer as a carrier
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/20—Compounding polymers with additives, e.g. colouring
- C08J3/203—Solid polymers with solid and/or liquid additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2201/00—Foams characterised by the foaming process
- C08J2201/02—Foams characterised by the foaming process characterised by mechanical pre- or post-treatments
- C08J2201/036—Use of an organic, non-polymeric compound to impregnate, bind or coat a foam, e.g. fatty acid ester
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/26—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2467/00—Characterised by the use of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Derivatives of such polymers
- C08J2467/04—Polyesters derived from hydroxy carboxylic acids, e.g. lactones
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/019—Specific properties of additives the composition being defined by the absence of a certain additive
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
したがって、本発明は、多孔性(これは当該マトリックスの体積に対する空隙の百分率として表される)が0.1vol%〜80vol%であるポリマーマトリックスに分散される二量体型及び/又は三量体型の環状ケトンペルオキシドを含むマスターバッチであって、100gのポリマーマトリックスあたり、1g〜30gの二量体型及び/又は三量体型の環状ケトンペルオキシドと、0.20g未満の、17個〜51個の炭素原子を有する飽和炭化水素とを含むマスターバッチに関連する。
ペンタンにおける24wt%の環状三量体型メチルエチルケトン(MEK)ペルオキシドの配合物を、36vol%の多孔性を有するポリプロピレンに吸収させた。これを、配合物を撹拌しながら前記ポリプロピレンにゆっくり加えることによって行った。
ペルオキシドのマスターバッチを、Isopar Mにおける環状三量体型MEKペルオキシド溶液を実施例1で使用されるポリプロピレンの表面に配合することによって調製した。環状三量体型MEKペルオキシドの最終含有量(純ペルオキシドとして)が10wt%及び12wt%であった。
Claims (13)
- 多孔性(これは当該マトリックスの体積に対する空隙の百分率として表される)が0.1vol%〜80vol%であるポリマーマトリックスに分散される二量体型及び/又は三量体型の環状ケトンペルオキシドを含むマスターバッチであって、100gのポリマーマトリックスあたり、1g〜30gの二量体型及び/又は三量体型の環状ケトンペルオキシドと、0.20g未満の、17個〜51個の炭素原子を有する飽和炭化水素とを含むマスターバッチ。
- 100gのポリマーマトリックスあたり、0.15g未満の、17個〜51個の炭素原子を有する飽和炭化水素を含む、請求項1に記載のマスターバッチ。
- 100gのポリマーマトリックスあたり、0.10g未満の、17個〜51個の炭素原子を有する飽和炭化水素を含む、請求項2に記載のマスターバッチ。
- 前記二量体型の環状ケトンペルオキシドが下記の式(I)による構造を有し、かつ、前記三量体型の環状ケトンペルオキシドが下記の式(II)による構造を有する、請求項1から3のいずれか一項に記載のマスターバッチ:
(式中、R1〜R6は独立して、水素、C1〜C20アルキル、C3〜C20シクロアルキル、C6〜C20アリール、C7〜C20アラルキル及びC7〜C20アルカリール(但し、これらの基は線状アルキル成分又は分岐アルキル成分を含む場合がある)からなる群から選択され、かつ、R1〜R6のそれぞれが必要な場合には、ヒドロキシ、アルコキシ、線状アルキル又は分岐アルキル、アリールオキシ、エステル、カルボキシ、ニトリル及びアミドから選択される1つ又はそれ以上の基により置換される場合がある)。 - 前記環状ケトンペルオキシドが3,6,9−トリエチル−3,6,9−トリメチル−1,4,7−トリペルオキソナンである、請求項4に記載のマスターバッチ。
- 得られたマスターバッチが、100gのポリマーマトリックスあたり4g〜18gの二量体型及び/又は三量体型の環状ケトンペルオキシドを含む、請求項1から5のいずれか一項に記載のマスターバッチ。
- 前記ポリマーマトリックスが10vol%〜60vol%の多孔性を有する、請求項1から6のいずれか一項に記載のマスターバッチ。
- 前記ポリマーマトリックスが、少なくとも50wt%の、ポリプロピレン、ポリエチレン、および/または、エチレンビニルアセタートポリマーからなる、請求項1から7のいずれか一項に記載のマスターバッチ。
- 配合物が1つ又はそれ以上さらなるペルオキシド又はヒドロペルオキシドを含む、請求項1から8のいずれか一項に記載のマスターバッチ。
- 請求項1から9に記載されるマスターバッチを調製するためのプロセスであって、下記の工程:
(i)多孔性(これは当該マトリックスの体積に対する空隙の百分率として表される)が0.1vol%〜80vol%であるポリマーマトリックスを提供する工程、並びに、
(ii)前記ポリマーマトリックスに、二量体型及び/又は三量体型の環状ケトンペルオキシドと1つ又はそれ以上の溶媒とを含む配合物を含浸する工程
を含むプロセス。 - ポリマーを改質するための、請求項1から9に記載されるマスターバッチの使用。
- 前記改質が、ポリプロピレンホモポリマー及び/又はプロピレンとエチレンとのコポリマーのクラッキングを伴う、請求項11に記載の使用。
- 前記改質がポリエチレンの長鎖分岐の導入又はポリエチレンの架橋を伴う、請求項11に記載の使用。
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201261733556P | 2012-12-05 | 2012-12-05 | |
US61/733,556 | 2012-12-05 | ||
EP13150128.0 | 2013-01-03 | ||
EP13150128 | 2013-01-03 | ||
PCT/EP2013/075191 WO2014086692A1 (en) | 2012-12-05 | 2013-12-02 | Masterbatch comprising a cyclic ketone peroxide |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2015537093A JP2015537093A (ja) | 2015-12-24 |
JP6138272B2 true JP6138272B2 (ja) | 2017-05-31 |
Family
ID=47627965
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2015545753A Active JP6138272B2 (ja) | 2012-12-05 | 2013-12-02 | 環状ケトンペルオキシドを含むマスターバッチ |
Country Status (8)
Country | Link |
---|---|
US (1) | US10316162B2 (ja) |
EP (1) | EP2928950B1 (ja) |
JP (1) | JP6138272B2 (ja) |
KR (1) | KR102179454B1 (ja) |
CN (1) | CN104822752B (ja) |
PL (1) | PL2928950T3 (ja) |
SG (1) | SG11201504016VA (ja) |
WO (1) | WO2014086692A1 (ja) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5980444B2 (ja) | 2012-12-05 | 2016-08-31 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | バイオ樹脂に基づくペルオキシドマスターバッチ |
JP6682101B2 (ja) * | 2016-06-08 | 2020-04-15 | 日本電信電話株式会社 | レーザ分光式安定同位体比分析法、装置、および多地点安定同位体比分析システム |
WO2018012583A1 (ja) * | 2016-07-14 | 2018-01-18 | 株式会社カネカ | 脂肪族ポリエステル樹脂組成物の製造方法 |
JP7340247B2 (ja) * | 2019-10-10 | 2023-09-07 | 株式会社バイオマステクノロジー | 簡便で工業性に優れた高濃度バイオマスポリオレフィン複合材料の製造方法 |
CN114656686A (zh) * | 2022-02-18 | 2022-06-24 | 任国辉 | 环状过氧化物在塑料造粒中的应用 |
Family Cites Families (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3301813A (en) | 1963-03-22 | 1967-01-31 | Monsanto Co | Process for incorporating a liquid additive into a solid thermoplastic polymer |
US4225650A (en) | 1975-10-22 | 1980-09-30 | Exxon Research & Engineering Co. | Crosslinkable polymer powder and laminate |
JPS541386A (en) | 1977-06-07 | 1979-01-08 | Nippon I P Rubber Kk | Manufacture of thermoplastic elastomer |
JPS5698247A (en) | 1979-12-29 | 1981-08-07 | Mitsubishi Petrochem Co Ltd | Partially crosslinking composition and partially crosslinked article |
JPS61255948A (ja) | 1985-05-09 | 1986-11-13 | Japan Synthetic Rubber Co Ltd | 熱可塑性エラストマ−配合物 |
BR8804014A (pt) | 1988-07-29 | 1989-04-11 | Konstantin Makedonsky | Processo de preparacao de concentrado de peroxidos organicos em borrachas sinteticas e polimeros |
CA2022349C (en) | 1989-10-13 | 2001-07-17 | Daryl L. Stein | Peroxide masterbatches using polycaprolactone as the carrier |
IT1240647B (it) | 1990-05-14 | 1993-12-17 | Himont Inc | Concentrati non estrusi di addittivi, cariche o pigmenti |
IT1260495B (it) * | 1992-05-29 | 1996-04-09 | Himont Inc | Concentrati adatti alla preparazione di poliolefine funzionalizzate e processo di funzionalizzazione mediante detti concentrati |
CH685877A5 (de) | 1993-11-03 | 1995-10-31 | Brugg Ag Kabelwerke | Verfahren zur Herstellung von Formteilen aus vernetzten Polymeren |
CZ18497A3 (en) * | 1994-07-21 | 1997-07-16 | Akzo Nobel Nv | Cyclic ketoneperoxidic compounds |
DE4437465A1 (de) | 1994-10-19 | 1996-04-25 | Peroxid Chemie Gmbh | Organische Peroxide enthaltende Masterbatch-Zusammensetzung |
KR20000069953A (ko) | 1997-02-03 | 2000-11-25 | 샬크비즈크 피이터 코르넬리스 | 안정성을 갖는 퍼옥시드 조성물 |
DE19805085A1 (de) * | 1998-02-09 | 1999-09-16 | Bayer Ag | Neue polymerisationsinitiierende geträgerte Systeme zur radikalischen Polymerisation von konjugierten Dienen und zur Copolymerisation dieser mit weiteren Monomeren in Suspensions- oder Gasphasenverfahren |
PL347265A1 (en) | 1998-10-16 | 2002-03-25 | Akzo Nobel Nv | Improved phlegmatization of cyclic ketone peroxides |
KR100387735B1 (ko) * | 1999-02-03 | 2003-06-18 | 삼성종합화학주식회사 | 유기과산화물 마스터뱃치 및 그 제조방법 |
AU782599B2 (en) | 2000-09-15 | 2005-08-11 | Baselltech Usa Inc. | Nonextruded dispersions and concentrates of additives on olefin polymers |
CH694461A5 (de) | 2000-12-08 | 2005-01-31 | Brugg Ag Kabelwerke | Schüttfähige thermoplastische Trägerpolymeren mit integrierten Additiven. |
JP4210448B2 (ja) | 2001-10-30 | 2009-01-21 | 日本ポリプロ株式会社 | マスターバッチ及びこれを用いた成形体 |
AU2002366330A1 (en) | 2001-12-13 | 2003-06-30 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcaninates for run-flat tires |
CN1315934C (zh) | 2002-03-12 | 2007-05-16 | 巴塞尔聚烯烃意大利有限公司 | 用于制备耐冲击聚烯烃制品的聚烯烃母料 |
DE10220038A1 (de) | 2002-05-04 | 2003-11-20 | Membrana Gmbh | Verfahren zur Herstellung geschäumter Polymerformkörper und geschäumter Polymerformkörper |
DE10220606A1 (de) | 2002-05-08 | 2003-11-20 | Peroxid Chemie Gmbh & Co Kg | Zubereitung für organische Peroxide |
AU2003292135A1 (en) | 2002-12-06 | 2004-06-30 | Akzo Nobel N.V. | Cyclic ketone peroxide formulations |
US20060128907A1 (en) | 2002-12-12 | 2006-06-15 | Yu Thomas C | Process for making a thermoplastic vulcanizates |
US7198844B2 (en) | 2003-01-17 | 2007-04-03 | Crompton Corporation | Microporous polymeric resin containing stabilizers and method for making thereof |
JP2004307538A (ja) | 2003-04-02 | 2004-11-04 | Sumitomo Chem Co Ltd | 変性ポリオレフィン系樹脂の製造方法及び変性ポリオレフィン系樹脂 |
EP1644432A1 (de) | 2003-07-03 | 2006-04-12 | Membrana GmbH | Träger für wässrige medien |
JP2005105101A (ja) | 2003-09-30 | 2005-04-21 | Nof Corp | 多孔質ポリオレフィン、その製造方法 |
US20060258796A1 (en) | 2005-05-13 | 2006-11-16 | General Electric Company | Crosslinked polyethylene compositions |
US7550532B2 (en) | 2005-07-11 | 2009-06-23 | Illinois Tool Works Inc. | Polyester resin composition |
IES20060903A2 (en) | 2005-12-12 | 2007-07-25 | Crownstone Ltd | A process for preparing a polyolefin masterbatch |
US20070232757A1 (en) | 2006-04-03 | 2007-10-04 | Kevin Cai | Mar resistant, glossy thermoplastic polyolefin blends and articles |
TWI453250B (zh) | 2007-11-08 | 2014-09-21 | Dainichiseika Color Chem | A method for producing a polyester resin molded article, a resin crystallization inducing agent, a masterbatch and a polyester resin molded product |
FR2946653B1 (fr) | 2009-06-15 | 2012-08-03 | Arkema France | Procede de fabrication d'une composition melange-maitre comprenant un peroxyde organique |
CN101649028B (zh) | 2009-09-18 | 2011-02-09 | 登封鼎盛工程塑料制品有限公司 | 工程塑料所用增韧母料 |
JP5980444B2 (ja) | 2012-12-05 | 2016-08-31 | アクゾ ノーベル ケミカルズ インターナショナル ベスローテン フエンノートシャップAkzo Nobel Chemicals International B.V. | バイオ樹脂に基づくペルオキシドマスターバッチ |
-
2013
- 2013-12-02 EP EP13798671.7A patent/EP2928950B1/en active Active
- 2013-12-02 SG SG11201504016VA patent/SG11201504016VA/en unknown
- 2013-12-02 JP JP2015545753A patent/JP6138272B2/ja active Active
- 2013-12-02 CN CN201380061349.XA patent/CN104822752B/zh active Active
- 2013-12-02 KR KR1020157014059A patent/KR102179454B1/ko active IP Right Grant
- 2013-12-02 US US14/648,801 patent/US10316162B2/en active Active
- 2013-12-02 PL PL13798671T patent/PL2928950T3/pl unknown
- 2013-12-02 WO PCT/EP2013/075191 patent/WO2014086692A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
KR20150091056A (ko) | 2015-08-07 |
WO2014086692A1 (en) | 2014-06-12 |
EP2928950A1 (en) | 2015-10-14 |
JP2015537093A (ja) | 2015-12-24 |
EP2928950B1 (en) | 2018-10-17 |
PL2928950T3 (pl) | 2019-04-30 |
SG11201504016VA (en) | 2015-06-29 |
CN104822752B (zh) | 2017-04-19 |
US20150291761A1 (en) | 2015-10-15 |
KR102179454B1 (ko) | 2020-11-18 |
US10316162B2 (en) | 2019-06-11 |
CN104822752A (zh) | 2015-08-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6138272B2 (ja) | 環状ケトンペルオキシドを含むマスターバッチ | |
JP5980444B2 (ja) | バイオ樹脂に基づくペルオキシドマスターバッチ | |
TWI602865B (zh) | 包含環酮過氧化物之母體混合物 | |
RU2655322C2 (ru) | Мастербатч, содержащий циклический пероксид кетона | |
RU2357954C2 (ru) | Составы с циклическими пероксидами кетонов, улучшенные составы с циклическими пероксидами кетонов | |
TWI607055B (zh) | 以生物樹脂爲基礎之過氧化物母體混合物 | |
TWI714680B (zh) | 降低高熔融強度聚丙烯之霧度之方法 | |
RU2654025C2 (ru) | Пероксидная маточная смесь на основе биосмолы | |
CN101657417A (zh) | 过氧化物组合物 | |
US3867461A (en) | Non-hazardous ketone peroxide compositions | |
JP2022545609A (ja) | 分岐を有するエチレン系ポリマー組成物 | |
BR112016019345B1 (pt) | Composição, processo para preparar uma composição de peróxido de cetona cíclica, composição de peróxido, e uso da composição | |
US20040162436A1 (en) | Cyclic ketone peroxide formulations | |
JPH0342212A (ja) | 発泡性スチレン系樹脂粒子の熟成方法 | |
FR3022251A1 (fr) | Solvant organique pour peroxydes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20150728 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20160708 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20160712 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20161012 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20170328 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20170425 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6138272 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |