KR102223325B1 - 폴리카바메이트 및 이의 반응 생성물을 제조하는 방법 - Google Patents
폴리카바메이트 및 이의 반응 생성물을 제조하는 방법 Download PDFInfo
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- KR102223325B1 KR102223325B1 KR1020167003890A KR20167003890A KR102223325B1 KR 102223325 B1 KR102223325 B1 KR 102223325B1 KR 1020167003890 A KR1020167003890 A KR 1020167003890A KR 20167003890 A KR20167003890 A KR 20167003890A KR 102223325 B1 KR102223325 B1 KR 102223325B1
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- IFDVQVHZEKPUSC-UHFFFAOYSA-N cyclohex-3-ene-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCC=CC1C(O)=O IFDVQVHZEKPUSC-UHFFFAOYSA-N 0.000 description 1
- XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 description 1
- DTPCFIHYWYONMD-UHFFFAOYSA-N decaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO DTPCFIHYWYONMD-UHFFFAOYSA-N 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- LDCRTTXIJACKKU-ARJAWSKDSA-N dimethyl maleate Chemical compound COC(=O)\C=C/C(=O)OC LDCRTTXIJACKKU-ARJAWSKDSA-N 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- 229940009714 erythritol Drugs 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- IIRDTKBZINWQAW-UHFFFAOYSA-N hexaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCO IIRDTKBZINWQAW-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- RXOHFPCZGPKIRD-UHFFFAOYSA-N naphthalene-2,6-dicarboxylic acid Chemical compound C1=C(C(O)=O)C=CC2=CC(C(=O)O)=CC=C21 RXOHFPCZGPKIRD-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 238000001208 nuclear magnetic resonance pulse sequence Methods 0.000 description 1
- GLZWNFNQMJAZGY-UHFFFAOYSA-N octaethylene glycol Chemical compound OCCOCCOCCOCCOCCOCCOCCOCCO GLZWNFNQMJAZGY-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- JLFNLZLINWHATN-UHFFFAOYSA-N pentaethylene glycol Chemical compound OCCOCCOCCOCCOCCO JLFNLZLINWHATN-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000006160 pyromellitic dianhydride group Chemical group 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- IBBQVGDGTMTZRA-UHFFFAOYSA-N sodium;2-sulfobenzene-1,3-dicarboxylic acid Chemical compound [Na].OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O IBBQVGDGTMTZRA-UHFFFAOYSA-N 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 238000007655 standard test method Methods 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
- UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 230000000007 visual effect Effects 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
- C08G71/00—Macromolecular compounds obtained by reactions forming a ureide or urethane link, otherwise, than from isocyanate radicals in the main chain of the macromolecule
- C08G71/04—Polyurethanes
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Polyurethanes Or Polyureas (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/955,507 | 2013-07-31 | ||
| US13/955,507 US9796815B2 (en) | 2013-07-31 | 2013-07-31 | Process for preparing polycarbamate and reaction product thereof |
| PCT/US2014/048347 WO2015017297A1 (en) | 2013-07-31 | 2014-07-28 | Process for preparing polycarbamate and reaction product thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20160036569A KR20160036569A (ko) | 2016-04-04 |
| KR102223325B1 true KR102223325B1 (ko) | 2021-03-04 |
Family
ID=51300906
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020167003890A Active KR102223325B1 (ko) | 2013-07-31 | 2014-07-28 | 폴리카바메이트 및 이의 반응 생성물을 제조하는 방법 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US9796815B2 (enExample) |
| EP (1) | EP3027674B1 (enExample) |
| JP (1) | JP6525379B2 (enExample) |
| KR (1) | KR102223325B1 (enExample) |
| CN (2) | CN105408392B (enExample) |
| CA (1) | CA2918949C (enExample) |
| WO (1) | WO2015017297A1 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3033376B1 (en) * | 2013-08-15 | 2022-12-28 | Dow Global Technologies LLC | Polycarbamate |
| EP2949687B1 (en) * | 2014-05-29 | 2016-10-19 | Dow Global Technologies Llc | Water feed methods to control mw distribution and byproducts of the carbamylation of urea |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030027075A1 (en) | 2001-02-27 | 2003-02-06 | Barclay George G. | Novel polymers, processes for polymer synthesis and photoresist compositions |
| JP2007505053A (ja) | 2003-09-11 | 2007-03-08 | ルルギ・アクチエンゲゼルシャフト | 有機カーボネート及びカルバメートの混合物から構成される中間生成物並びにそれらの製造方法 |
| JP2010150327A (ja) | 2008-12-24 | 2010-07-08 | Kao Corp | カルボン酸系重合体の製造方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2956964A (en) * | 1954-09-13 | 1960-10-18 | Pittsburgh Plate Glass Co | Composition comprising reaction product of aldehyde and polycarbamate and method of preparing |
| FR1403660A (fr) * | 1963-12-28 | 1965-06-25 | Kuhlmann Ets | Nouvelles résines alkydes et leurs applications |
| DE2620010A1 (de) * | 1976-05-06 | 1977-12-01 | Basf Ag | Gemische von pentaerythritcarbamaten mit polyalkylenglykolaethercarbamaten und mit alkylalkylenglykolcarbamaten und verfahren zu ihrer herstellung |
| US4443622A (en) * | 1981-05-15 | 1984-04-17 | West Point Pepperell, Inc. | Method for making carbamates |
| US4963643A (en) * | 1983-03-31 | 1990-10-16 | Amoco Corporation | Crystalline polyarylnitrile ether polymer |
| US4459397A (en) * | 1983-04-25 | 1984-07-10 | Wisconsin Alumni Research Foundation | Modified polyether polyol for preparation of polyurethane polymer |
| US5008103A (en) * | 1988-12-29 | 1991-04-16 | General Electric Company | Silicone surfactants |
| US5189117A (en) * | 1990-08-03 | 1993-02-23 | The Dow Chemical Company | Polyurethane from epoxy compound adduct |
| JP3476026B2 (ja) * | 1994-01-20 | 2003-12-10 | 大日本インキ化学工業株式会社 | 水性樹脂およびその製造法ならびに該水性樹脂を含有する水性塗料組成物 |
| US6444718B1 (en) * | 1996-09-30 | 2002-09-03 | David H. Blount | Aquerous urea for fire control |
| CN1088464C (zh) * | 1996-12-20 | 2002-07-31 | Ppg工业俄亥俄公司 | 用来改进经蒸汽处理的固化涂层的物理特性的涂料组合物 |
| US5795934A (en) * | 1997-05-20 | 1998-08-18 | Georgia-Pacific Resins, Jr. | Method for preparing a urea-extended phenolic resole resin stabilized with an alkanolamine |
| WO2001047870A2 (en) * | 1999-12-27 | 2001-07-05 | Huntsman International Llc | Process for the production of aromatic polycarbamates |
| CN1173939C (zh) * | 2001-01-16 | 2004-11-03 | 西北大学 | 氨基甲酸酯的制备方法 |
| EP2397506B1 (en) * | 2010-06-16 | 2017-09-27 | Dow Global Technologies Inc. | Ambient temperature curable isocyanate-free compositions for preparing crosslinked polyurethanes |
| US9290675B2 (en) * | 2013-06-18 | 2016-03-22 | Dow Global Technologies Llc | Crosslinkable coating composition and method of producing the same |
-
2013
- 2013-07-31 US US13/955,507 patent/US9796815B2/en active Active
-
2014
- 2014-07-28 EP EP14750132.4A patent/EP3027674B1/en active Active
- 2014-07-28 WO PCT/US2014/048347 patent/WO2015017297A1/en not_active Ceased
- 2014-07-28 JP JP2016531784A patent/JP6525379B2/ja active Active
- 2014-07-28 CN CN201480040336.9A patent/CN105408392B/zh active Active
- 2014-07-28 CA CA2918949A patent/CA2918949C/en active Active
- 2014-07-28 CN CN201811243832.0A patent/CN109337067A/zh active Pending
- 2014-07-28 KR KR1020167003890A patent/KR102223325B1/ko active Active
-
2017
- 2017-09-22 US US15/712,181 patent/US20180009947A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030027075A1 (en) | 2001-02-27 | 2003-02-06 | Barclay George G. | Novel polymers, processes for polymer synthesis and photoresist compositions |
| JP2007505053A (ja) | 2003-09-11 | 2007-03-08 | ルルギ・アクチエンゲゼルシャフト | 有機カーボネート及びカルバメートの混合物から構成される中間生成物並びにそれらの製造方法 |
| JP2010150327A (ja) | 2008-12-24 | 2010-07-08 | Kao Corp | カルボン酸系重合体の製造方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US9796815B2 (en) | 2017-10-24 |
| JP2016527363A (ja) | 2016-09-08 |
| EP3027674B1 (en) | 2023-06-14 |
| CN109337067A (zh) | 2019-02-15 |
| CN105408392A (zh) | 2016-03-16 |
| EP3027674A1 (en) | 2016-06-08 |
| JP6525379B2 (ja) | 2019-06-05 |
| CN105408392B (zh) | 2018-11-16 |
| CA2918949C (en) | 2021-12-14 |
| US20180009947A1 (en) | 2018-01-11 |
| US20150038670A1 (en) | 2015-02-05 |
| CA2918949A1 (en) | 2015-02-05 |
| WO2015017297A1 (en) | 2015-02-05 |
| KR20160036569A (ko) | 2016-04-04 |
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