KR940007078A - 이중 금속 시안화물 촉매로써 제조된 폴리올의 정제방법 - Google Patents
이중 금속 시안화물 촉매로써 제조된 폴리올의 정제방법 Download PDFInfo
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- KR940007078A KR940007078A KR1019930019258A KR930019258A KR940007078A KR 940007078 A KR940007078 A KR 940007078A KR 1019930019258 A KR1019930019258 A KR 1019930019258A KR 930019258 A KR930019258 A KR 930019258A KR 940007078 A KR940007078 A KR 940007078A
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- KR
- South Korea
- Prior art keywords
- polyol
- aliphatic alcohol
- process according
- polyether polyol
- range
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract 15
- 229920005862 polyol Polymers 0.000 title claims abstract 15
- 150000003077 polyols Chemical class 0.000 title claims abstract 15
- 239000003054 catalyst Substances 0.000 title claims abstract 8
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 title claims abstract 4
- 229910052751 metal Inorganic materials 0.000 title claims abstract 3
- 239000002184 metal Substances 0.000 title claims abstract 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract 8
- 229920000570 polyether Polymers 0.000 claims abstract 8
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract 7
- 239000002738 chelating agent Substances 0.000 claims abstract 5
- 239000000203 mixture Substances 0.000 claims abstract 3
- 150000001768 cations Chemical class 0.000 claims abstract 2
- 238000001914 filtration Methods 0.000 claims abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims 2
- 239000004698 Polyethylene Substances 0.000 claims 2
- 229960001484 edetic acid Drugs 0.000 claims 2
- -1 polyethylene Polymers 0.000 claims 2
- 229920000573 polyethylene Polymers 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 239000011777 magnesium Substances 0.000 claims 1
- 229910052749 magnesium Inorganic materials 0.000 claims 1
- 229910052700 potassium Inorganic materials 0.000 claims 1
- 239000011591 potassium Substances 0.000 claims 1
- 238000000746 purification Methods 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 239000011701 zinc Substances 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 229920005903 polyol mixture Polymers 0.000 abstract 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
- 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
- C08G65/26—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 from cyclic ethers and other compounds
- C08G65/2642—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 from cyclic ethers and other compounds characterised by the catalyst used
- C08G65/2645—Metals or compounds thereof, e.g. salts
- C08G65/2663—Metal cyanide catalysts, i.e. DMC's
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/24—Nitrogen compounds
- B01J27/26—Cyanides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/34—Separation; Purification; Stabilisation; Use of additives
- C07C41/44—Separation; Purification; Stabilisation; Use of additives by treatments giving rise to a chemical modification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/10—Saturated ethers of polyhydroxy compounds
- C07C43/11—Polyethers containing —O—(C—C—O—)n units with ≤ 2 n≤ 10
-
- 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
- C08G65/30—Post-polymerisation treatment, e.g. recovery, purification, drying
-
- 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
- C08G65/34—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from hydroxy compounds or their metallic derivatives
- C08G65/46—Post-polymerisation treatment, e.g. recovery, purification, drying
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Toxicology (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Polyethers (AREA)
Abstract
이중 금속 시안화물(DMC) 촉매를 사용하여 제조된 폴리에테르 폴리올의 정제 방법이 개시된다. 이 방법은 폴리올과 C1-C6지방족 알코올의 혼합물을 촉매와 불용성 착물을 형성하기에 유효한 량의 킬레이트제와 결합시킨 다음, 폴리올 혼합물을 여과하여 불용성 착물을 제거하는 것이 포함된다. 이 방법은 폴리올과 알코올이 1:1 내지 100:1의 상대 중량비로 존재할 것을 조건으로 하며, DMC 찌꺼기와 킬레이트제로써 도입된 모든 양이온을 효과적으로 제거한다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (12)
- (a) 이중 금속 시안화물 촉매 찌꺼기를 함유하는 폴리에테르 폴리올을 C1-C8지방족 알코올과, 촉매 찌꺼기와 불용성 착물을 형성하기에 유효한 양의 킬레이트제와 결합시키고; (b) 얻어진 혼합물을 여과하여 폴리올로부터 불용성 착물을 제거하는; (상기에서 폴리에테르 폴리올 대 C1-C6지방족 알코올의 상대 중량비는 1:1 내지 100:1 범위내이다.) 것으로 이루어짐을 특징으로 하는 이중금속 시안화물 촉매를 사용하여 제조된 폴리에테르 폴리올의 정제방법.
- 제1항에 있어서, 킬레이트제는 에틸렌 디아민 테트라아세트산(EDTA)과 리튬, 나트륨, 칼륨, 마그네슘, 칼슘, 암모늄 및 철로 구성되는 군에서 선택되는 하나 또는 그 이상의 양이온을 함유하는 EDTA 염으로 구성되는 군에서 선택됨을 특징으로 하는 방법.
- 제1항에 있어서, 폴리에테르 폴리올 대 C1-C6지방족 알코올의 상대 중량비는 2:1 내지 10:1 범위내임을 특징으로 하는 방법
- 제2항에 있어서, 폴리에테르 폴리올 대 C1-C6지방족 알코올의 상대 중량비가 2:1 내지 10:1 범위내임을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, 폴리에테르 폴리올의 공칭관능가가 1 내지 8인 것을 특징으로 하는 방법.
- 제1 내지 제4항중 어느 한 항에 있어서, 폴리에틸렌 폴리올이 에틸렌 옥사이드와 프로필렌 옥사이드의 공중합체인 것을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, 폴리에틸렌 폴리올의 수평균 분자량이 250 내지 25,000 범위내인 것을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, 촉매 찌꺼기는 헥사시아노코발트산 아연 촉매로부터 유도되는 것임을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, C1-C6지방족 알코올은 메탄올, 에탄올, n-프로판올 및 이소프로필 알코올로 구성되는 군에서 선택됨을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, C1-C4지방족 알코올을 함유하는 물과의 혼합물을 사용함을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항에 있어서, 결합되는 폴리올, 알코올 및 킬레이트제를 20℃ 내지 80℃ 범위내의 온도에서 결합시키는 것을 특징으로 하는 방법.
- 제1 내지 4항중 어느 한 항의 방법에 의해 제조된, 정제된 폴리에테르 폴리올.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/948,275 US5248833A (en) | 1992-09-22 | 1992-09-22 | Process for purifying polyols made with double metal cyanide catalysts |
US7/948,275 | 1992-09-22 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR940007078A true KR940007078A (ko) | 1994-04-26 |
KR100285866B1 KR100285866B1 (ko) | 2001-04-16 |
Family
ID=25487580
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930019258A KR100285866B1 (ko) | 1992-09-22 | 1993-09-22 | 이중 금속 시안화물 촉매를 사용하여 제조된 폴리올의 정제방법 |
Country Status (11)
Country | Link |
---|---|
US (1) | US5248833A (ko) |
EP (1) | EP0589635B1 (ko) |
JP (1) | JP3397392B2 (ko) |
KR (1) | KR100285866B1 (ko) |
AU (1) | AU663973B2 (ko) |
BR (1) | BR9303854A (ko) |
CA (1) | CA2106184C (ko) |
DE (1) | DE69315161T2 (ko) |
ES (1) | ES2109442T3 (ko) |
MX (1) | MX9305758A (ko) |
TW (1) | TW253892B (ko) |
Cited By (1)
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KR100581741B1 (ko) * | 1999-04-29 | 2006-05-23 | 비와이케이-케미 게엠베하 | 요변성제의 제조 방법 및 그 용도 |
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DE60317652T2 (de) * | 2003-06-30 | 2008-10-30 | Repsol Quimica S.A. | Verfahren zur Reinigung von Polyetherpolyolen |
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WO1990007537A1 (en) * | 1989-01-06 | 1990-07-12 | Asahi Glass Company Ltd. | Production of polyether |
US4987271A (en) * | 1989-02-17 | 1991-01-22 | Asahi Glass Company, Ltd. | Method for purifying a polyoxyalkylene alcohol |
US5010047A (en) * | 1989-02-27 | 1991-04-23 | Arco Chemical Technology, Inc. | Recovery of double metal cyanide complex catalyst from a polymer |
JPH0747631B2 (ja) * | 1990-05-21 | 1995-05-24 | 旭化成工業株式会社 | ポリフェニレンエーテルの製造方法 |
US5099075A (en) * | 1990-11-02 | 1992-03-24 | Olin Corporation | Process for removing double metal cyanide catalyst residues from a polyol |
US5144093A (en) * | 1991-04-29 | 1992-09-01 | Olin Corporation | Process for purifying and end-capping polyols made using double metal cyanide catalysts |
US5158922A (en) * | 1992-02-04 | 1992-10-27 | Arco Chemical Technology, L.P. | Process for preparing metal cyanide complex catalyst |
-
1992
- 1992-09-22 US US07/948,275 patent/US5248833A/en not_active Expired - Lifetime
-
1993
- 1993-09-14 CA CA002106184A patent/CA2106184C/en not_active Expired - Fee Related
- 1993-09-17 ES ES93307364T patent/ES2109442T3/es not_active Expired - Lifetime
- 1993-09-17 EP EP93307364A patent/EP0589635B1/en not_active Expired - Lifetime
- 1993-09-17 DE DE69315161T patent/DE69315161T2/de not_active Expired - Fee Related
- 1993-09-21 MX MX9305758A patent/MX9305758A/es not_active IP Right Cessation
- 1993-09-21 BR BR9303854A patent/BR9303854A/pt not_active IP Right Cessation
- 1993-09-22 AU AU47530/93A patent/AU663973B2/en not_active Ceased
- 1993-09-22 KR KR1019930019258A patent/KR100285866B1/ko not_active IP Right Cessation
- 1993-09-22 TW TW082107809A patent/TW253892B/zh active
- 1993-09-22 JP JP25746993A patent/JP3397392B2/ja not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100581741B1 (ko) * | 1999-04-29 | 2006-05-23 | 비와이케이-케미 게엠베하 | 요변성제의 제조 방법 및 그 용도 |
Also Published As
Publication number | Publication date |
---|---|
AU663973B2 (en) | 1995-10-26 |
ES2109442T3 (es) | 1998-01-16 |
EP0589635B1 (en) | 1997-11-12 |
BR9303854A (pt) | 1994-05-10 |
EP0589635A1 (en) | 1994-03-30 |
US5248833A (en) | 1993-09-28 |
CA2106184C (en) | 2005-01-11 |
DE69315161T2 (de) | 1998-03-12 |
JPH06200013A (ja) | 1994-07-19 |
AU4753093A (en) | 1994-03-31 |
JP3397392B2 (ja) | 2003-04-14 |
KR100285866B1 (ko) | 2001-04-16 |
TW253892B (ko) | 1995-08-11 |
CA2106184A1 (en) | 1994-03-23 |
MX9305758A (es) | 1994-05-31 |
DE69315161D1 (de) | 1997-12-18 |
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