JP4118504B2 - ポリオレフィン/ポリオレフィン・ブロック共重合体 - Google Patents
ポリオレフィン/ポリオレフィン・ブロック共重合体 Download PDFInfo
- Publication number
- JP4118504B2 JP4118504B2 JP2000358226A JP2000358226A JP4118504B2 JP 4118504 B2 JP4118504 B2 JP 4118504B2 JP 2000358226 A JP2000358226 A JP 2000358226A JP 2000358226 A JP2000358226 A JP 2000358226A JP 4118504 B2 JP4118504 B2 JP 4118504B2
- Authority
- JP
- Japan
- Prior art keywords
- ipp
- polyolefin
- block copolymer
- oligopropylene
- highly controlled
- 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.)
- Expired - Fee Related
Links
- 229920001400 block copolymer Polymers 0.000 title claims description 12
- 229920000098 polyolefin Polymers 0.000 title description 18
- 238000000197 pyrolysis Methods 0.000 claims description 8
- 239000004743 Polypropylene Substances 0.000 claims description 7
- -1 polypropylene Polymers 0.000 claims description 7
- 229920001155 polypropylene Polymers 0.000 claims description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 238000005886 esterification reaction Methods 0.000 claims description 2
- FQYQMFCIJNWDQZ-CYDGBPFRSA-N Ile-Pro-Pro Chemical compound CC[C@H](C)[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1[C@H](C(O)=O)CCC1 FQYQMFCIJNWDQZ-CYDGBPFRSA-N 0.000 claims 1
- 230000000640 hydroxylating effect Effects 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 150000001336 alkenes Chemical class 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 3
- 238000002329 infrared spectrum Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 229920005606 polypropylene copolymer Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 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
- 238000001914 filtration Methods 0.000 description 1
- 238000006197 hydroboration reaction Methods 0.000 description 1
- 230000033444 hydroxylation Effects 0.000 description 1
- 238000005805 hydroxylation reaction Methods 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Images
Landscapes
- Polyesters Or Polycarbonates (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Priority Applications (15)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000358226A JP4118504B2 (ja) | 2000-11-24 | 2000-11-24 | ポリオレフィン/ポリオレフィン・ブロック共重合体 |
| DE60137463T DE60137463D1 (de) | 2000-11-24 | 2001-11-22 | funktionale substanzen aus oligoolefinen mit funktionalen endgruppen |
| HK04110142.2A HK1067135B (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| DE60143490T DE60143490D1 (de) | 2000-11-24 | 2001-11-22 | Von oligoolefinen mit funktionellen endgruppen abgeleitete funktionelle substanzen |
| AU2002224085A AU2002224085A1 (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| CNB01819429XA CN100558758C (zh) | 2000-11-24 | 2001-11-22 | 从有末端官能团的低聚烯烃衍生的功能性物质 |
| EP07001650A EP1790669B1 (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| CN200810181676XA CN101486779B (zh) | 2000-11-24 | 2001-11-22 | 从有末端官能团的低聚烯烃衍生的功能性物质 |
| EP01997195A EP1364973B1 (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| KR10-2003-7006981A KR100501968B1 (ko) | 2000-11-24 | 2001-11-22 | 말단 관능성기를 갖는 올리고올레핀으로부터 유도되는기능성 물질류 |
| PCT/JP2001/010244 WO2002042340A1 (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| US10/416,615 US7125834B2 (en) | 2000-11-24 | 2001-11-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| HK09110762.6A HK1133025B (en) | 2000-11-24 | 2004-12-22 | Functional substances derived from oligoolefins having functional groups at the ends |
| US11/440,900 US7229957B2 (en) | 2000-11-24 | 2006-05-25 | Functional substances derived from oligoolefins having functional groups at the ends |
| US11/654,751 US7345017B2 (en) | 2000-11-24 | 2007-01-18 | Functional substances derived from oligoolefins having functional groups at the ends |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000358226A JP4118504B2 (ja) | 2000-11-24 | 2000-11-24 | ポリオレフィン/ポリオレフィン・ブロック共重合体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2002161142A JP2002161142A (ja) | 2002-06-04 |
| JP2002161142A5 JP2002161142A5 (enExample) | 2007-07-19 |
| JP4118504B2 true JP4118504B2 (ja) | 2008-07-16 |
Family
ID=18830167
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000358226A Expired - Fee Related JP4118504B2 (ja) | 2000-11-24 | 2000-11-24 | ポリオレフィン/ポリオレフィン・ブロック共重合体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4118504B2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002161111A (ja) * | 2000-11-24 | 2002-06-04 | Takashi Sawaguchi | 末端パーフルオロアルキル基含有オレフィン・オリゴマーおよびその製造方法 |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4866988B2 (ja) * | 2001-07-30 | 2012-02-01 | Jnc株式会社 | アイソタクチック−アタクチック−ブロックポリプロピレン |
| JP4012058B2 (ja) | 2001-12-21 | 2007-11-21 | キヤノン株式会社 | リサイクル性重合体、その製造方法、ならびにリサイクル処理方法 |
| JP2007518870A (ja) * | 2004-01-22 | 2007-07-12 | ダウ グローバル テクノロジーズ インコーポレイティド | 官能基化されたエラストマー組成物 |
| JP5344819B2 (ja) * | 2005-07-12 | 2013-11-20 | 三井化学株式会社 | ポリオレフィン系ハイブリッドポリマーおよびその製造方法 |
| JP5248909B2 (ja) * | 2007-12-10 | 2013-07-31 | 孝志 澤口 | 両末端ハロゲン化オリゴオレフィン及びそれを用いたトリブロック共重合体 |
| JP6125762B2 (ja) * | 2012-05-14 | 2017-05-10 | 株式会社三栄興業 | テレケリックアイオノマー及びその製造方法 |
| JP2023046712A (ja) * | 2021-09-24 | 2023-04-05 | 三洋化成工業株式会社 | 変性ポリオレフィン |
-
2000
- 2000-11-24 JP JP2000358226A patent/JP4118504B2/ja not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002161111A (ja) * | 2000-11-24 | 2002-06-04 | Takashi Sawaguchi | 末端パーフルオロアルキル基含有オレフィン・オリゴマーおよびその製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002161142A (ja) | 2002-06-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Chung | Synthesis of polyalcohols via Ziegler-Natta polymerization | |
| KR100565155B1 (ko) | 폴리올레핀 마크로모노머, 그 폴리올레핀마크로모노머로부터 얻어지는 그래프트 중합체, 및 그 용도 | |
| JP4118504B2 (ja) | ポリオレフィン/ポリオレフィン・ブロック共重合体 | |
| Mecerreyes et al. | Synthesis of dendritic–linear block copolymers by living ring‐opening polymerization of lactones and lactides using dendritic initiators | |
| US7125834B2 (en) | Functional substances derived from oligoolefins having functional groups at the ends | |
| TWI301838B (en) | Multi-branched polymer, process for producing the same, and applications thereof | |
| WO1998002472A1 (en) | New diblock copolymers consisting of polyolefin and functional polymer segments | |
| Kaneko et al. | Syntheses of graft and star copolymers possessing polyolefin branches by using polyolefin macromonomer | |
| CN114846056A (zh) | 基于聚丙烯酸酯的接枝共聚物 | |
| Srinivrasan et al. | Preparation of thermally labile PMMA particles by combined non-aqueous dispersion polymerization and polymer chain transfer | |
| JP4686022B2 (ja) | 末端マレイン化オリゴオレフィン/ジアミノポリジメチルシロキサン・マルチブロック共重合体およびその製造方法 | |
| Cazzaniga et al. | Synthesis and characterization of isotactic polystyrene/polybutadiene block copolymers | |
| Miura et al. | Well-defined graft copolymers of methacrylate, acrylate, and styrene via ruthenium-catalyzed living radical polymerization | |
| JP3853719B2 (ja) | 両末端チオール化オリゴプロピレン | |
| JP3059320B2 (ja) | 反応性オレフィン系重合体 | |
| TWI281475B (en) | Novel polyesterified block copolymer and process for producing the same | |
| Jiang et al. | Studies on the Synthesis of Ethylene Copolymers and Their Properties | |
| US5489651A (en) | Polymerization using bimetallic bis-lanthanoid initiators | |
| CN111072831A (zh) | 多功能极性聚烯烃材料及其金属配合物材料、制备方法和用途 | |
| JP2004339445A (ja) | 末端アミノ化ポリオレフィン及びその製造方法 | |
| JP2999307B2 (ja) | プロピレン/スチレンブロック共重合体及びその製造法 | |
| JP2639770B2 (ja) | ポリビニルアルコール系グラフト共重合体 | |
| JPH10510314A (ja) | 官能化p−アルキルスチレン重合体および共重合体 | |
| Nomura et al. | Synthesis of poly (tetrahydrofuran-b-ε-caprolactone) macromonomer via the Sml2-induced transformation | |
| JP4568584B2 (ja) | マルチブロック共重合体 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| RD03 | Notification of appointment of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7423 Effective date: 20040123 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20070601 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070601 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20070907 |
|
| A521 | Written amendment |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20071106 |
|
| 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: 20080410 |
|
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20080423 |
|
| R150 | Certificate of patent or registration of utility model |
Free format text: JAPANESE INTERMEDIATE CODE: R150 Ref document number: 4118504 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110502 Year of fee payment: 3 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20110502 Year of fee payment: 3 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130502 Year of fee payment: 5 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130502 Year of fee payment: 5 |
|
| FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140502 Year of fee payment: 6 |
|
| 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 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |