KR20100102629A - 트라이메틸렌 카보네이트의 폴리(트라이메틸렌 글리콜 카보네이트 트라이메틸렌 글리콜 에테르) 다이올에로의 무용매 중합법 - Google Patents
트라이메틸렌 카보네이트의 폴리(트라이메틸렌 글리콜 카보네이트 트라이메틸렌 글리콜 에테르) 다이올에로의 무용매 중합법 Download PDFInfo
- Publication number
- KR20100102629A KR20100102629A KR1020107014392A KR20107014392A KR20100102629A KR 20100102629 A KR20100102629 A KR 20100102629A KR 1020107014392 A KR1020107014392 A KR 1020107014392A KR 20107014392 A KR20107014392 A KR 20107014392A KR 20100102629 A KR20100102629 A KR 20100102629A
- Authority
- KR
- South Korea
- Prior art keywords
- carbonate
- trimethylene glycol
- trimethylene
- poly
- diol
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- -1 poly(trimethylene glycol carbonate trimethylene glycol Chemical compound 0.000 title claims abstract description 18
- 150000002009 diols Chemical class 0.000 title claims abstract description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000006116 polymerization reaction Methods 0.000 title abstract description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 title 1
- YFHICDDUDORKJB-UHFFFAOYSA-N trimethylene carbonate Chemical class O=C1OCCCO1 YFHICDDUDORKJB-UHFFFAOYSA-N 0.000 claims abstract description 23
- 239000003054 catalyst Substances 0.000 claims abstract description 16
- 239000011973 solid acid Substances 0.000 claims abstract description 8
- 125000001424 substituent group Chemical group 0.000 claims description 9
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 125000006737 (C6-C20) arylalkyl group Chemical group 0.000 claims description 4
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000003456 ion exchange resin Substances 0.000 claims description 3
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 3
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 claims description 2
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 12
- YPFDHNVEDLHUCE-UHFFFAOYSA-N Trimethylene glycol Natural products OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 11
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 description 10
- 229940035437 1,3-propanediol Drugs 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 6
- 229920000557 Nafion® Polymers 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 4
- 238000002835 absorbance Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 3
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000004417 polycarbonate Substances 0.000 description 3
- 229920000515 polycarbonate Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 3
- PMPVIKIVABFJJI-UHFFFAOYSA-N Cyclobutane Chemical compound C1CCC1 PMPVIKIVABFJJI-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- 102000004882 Lipase Human genes 0.000 description 2
- 108090001060 Lipase Proteins 0.000 description 2
- 239000004367 Lipase Substances 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 238000002306 biochemical method Methods 0.000 description 2
- 239000000560 biocompatible material Substances 0.000 description 2
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 2
- 239000004914 cyclooctane Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004817 gas chromatography Methods 0.000 description 2
- 229920000554 ionomer Polymers 0.000 description 2
- 235000019421 lipase Nutrition 0.000 description 2
- CKFGINPQOCXMAZ-UHFFFAOYSA-N methanediol Chemical compound OCO CKFGINPQOCXMAZ-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VWAHANAGQLJKOZ-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene 2-phenylethenesulfonic acid Chemical compound C=CC1=CC=CC=C1C=C.OS(=O)(=O)C=CC1=CC=CC=C1 VWAHANAGQLJKOZ-UHFFFAOYSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- SELFXCFVPOJKBE-UHFFFAOYSA-N 2-(1-ethenoxypropan-2-yloxy)ethanesulfonic acid Chemical compound C=COCC(C)OCCS(O)(=O)=O SELFXCFVPOJKBE-UHFFFAOYSA-N 0.000 description 1
- IOWJYMAPHQYKSB-UHFFFAOYSA-N 3-hydroxypropyl hydrogen carbonate Chemical compound OCCCOC(O)=O IOWJYMAPHQYKSB-UHFFFAOYSA-N 0.000 description 1
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- 235000019256 formaldehyde Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- VSPPONOIKZXUBJ-UHFFFAOYSA-N n,n-diethylethanamine;oxolane Chemical compound C1CCOC1.CCN(CC)CC VSPPONOIKZXUBJ-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000002076 thermal analysis method Methods 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/20—General preparatory processes
- C08G64/30—General preparatory processes using carbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
- C08G64/02—Aliphatic polycarbonates
- C08G64/0208—Aliphatic polycarbonates saturated
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US99168707P | 2007-11-30 | 2007-11-30 | |
| US60/991,687 | 2007-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20100102629A true KR20100102629A (ko) | 2010-09-24 |
Family
ID=40350063
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107014392A Withdrawn KR20100102629A (ko) | 2007-11-30 | 2008-11-25 | 트라이메틸렌 카보네이트의 폴리(트라이메틸렌 글리콜 카보네이트 트라이메틸렌 글리콜 에테르) 다이올에로의 무용매 중합법 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7790833B2 (enExample) |
| EP (1) | EP2215142B1 (enExample) |
| JP (1) | JP2011505468A (enExample) |
| KR (1) | KR20100102629A (enExample) |
| CN (1) | CN101878244A (enExample) |
| AT (1) | ATE538159T1 (enExample) |
| AU (1) | AU2008329778A1 (enExample) |
| BR (1) | BRPI0818996A2 (enExample) |
| CA (1) | CA2704022A1 (enExample) |
| ES (1) | ES2378359T3 (enExample) |
| MX (1) | MX2010005754A (enExample) |
| TW (1) | TW200934807A (enExample) |
| WO (1) | WO2009070587A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2444001A1 (en) | 2010-10-20 | 2012-04-25 | Samsung Medison Co., Ltd. | Providing an ultrasound spatial compound image based on a phased array probe in an ultrasound system |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2703786A1 (en) * | 2007-11-30 | 2009-06-04 | E.I. Du Pont De Nemours And Company | Process to make a poly(trimethylene carbonate) glycol |
| KR20100099713A (ko) * | 2007-11-30 | 2010-09-13 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 폴리(트라이메틸렌 글리콜 카보네이트 트라이메틸렌 글리콜 에테르) 다이올 조성물 및 이의 제조 방법 |
| WO2025197815A1 (ja) * | 2024-03-19 | 2025-09-25 | 富士フイルム株式会社 | ポリカーボネート化合物の製造方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05339360A (ja) * | 1992-06-12 | 1993-12-21 | Idemitsu Petrochem Co Ltd | ポリカーボネートの製造方法 |
| DE69317818T2 (de) * | 1992-07-13 | 1998-08-06 | Tosoh Corp | Verfahren zur Herstellung von tertiären Alkoholen |
| JPH0710920A (ja) * | 1992-12-01 | 1995-01-13 | Nippon Paint Co Ltd | 環状カーボネート化合物のアルコール性水酸基への開環付加方法 |
| JPH09176152A (ja) * | 1995-12-28 | 1997-07-08 | Sumitomo Bakelite Co Ltd | 環状カーボナート化合物の重合方法 |
| US6451949B2 (en) * | 2000-02-29 | 2002-09-17 | Shell Oil Company | Method for production of poly (trimethylene carbonate) |
| KR20100099713A (ko) * | 2007-11-30 | 2010-09-13 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 폴리(트라이메틸렌 글리콜 카보네이트 트라이메틸렌 글리콜 에테르) 다이올 조성물 및 이의 제조 방법 |
| WO2009070578A1 (en) * | 2007-11-30 | 2009-06-04 | E. I. Du Pont De Nemours And Company | Copolymers comprising a trimethylene carbonate and poly(trimethylene ether) glycols |
-
2008
- 2008-11-25 AU AU2008329778A patent/AU2008329778A1/en not_active Abandoned
- 2008-11-25 EP EP08855247A patent/EP2215142B1/en not_active Not-in-force
- 2008-11-25 CN CN2008801183093A patent/CN101878244A/zh active Pending
- 2008-11-25 JP JP2010536129A patent/JP2011505468A/ja active Pending
- 2008-11-25 KR KR1020107014392A patent/KR20100102629A/ko not_active Withdrawn
- 2008-11-25 AT AT08855247T patent/ATE538159T1/de active
- 2008-11-25 CA CA2704022A patent/CA2704022A1/en not_active Abandoned
- 2008-11-25 US US12/277,644 patent/US7790833B2/en not_active Expired - Fee Related
- 2008-11-25 ES ES08855247T patent/ES2378359T3/es active Active
- 2008-11-25 BR BRPI0818996 patent/BRPI0818996A2/pt not_active IP Right Cessation
- 2008-11-25 MX MX2010005754A patent/MX2010005754A/es active IP Right Grant
- 2008-11-25 WO PCT/US2008/084693 patent/WO2009070587A1/en not_active Ceased
- 2008-11-28 TW TW097146471A patent/TW200934807A/zh unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2444001A1 (en) | 2010-10-20 | 2012-04-25 | Samsung Medison Co., Ltd. | Providing an ultrasound spatial compound image based on a phased array probe in an ultrasound system |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008329778A1 (en) | 2009-06-04 |
| TW200934807A (en) | 2009-08-16 |
| CA2704022A1 (en) | 2009-06-04 |
| ES2378359T3 (es) | 2012-04-11 |
| US20090143564A1 (en) | 2009-06-04 |
| WO2009070587A1 (en) | 2009-06-04 |
| ATE538159T1 (de) | 2012-01-15 |
| MX2010005754A (es) | 2010-06-09 |
| BRPI0818996A2 (pt) | 2015-05-05 |
| US7790833B2 (en) | 2010-09-07 |
| CN101878244A (zh) | 2010-11-03 |
| EP2215142B1 (en) | 2011-12-21 |
| EP2215142A1 (en) | 2010-08-11 |
| JP2011505468A (ja) | 2011-02-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20100629 Patent event code: PA01051R01D Comment text: International Patent Application |
|
| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |