TWI461406B - 使用亞甲基醌／烷基羥胺組合之乙烯基芳族單體的聚合物抑制 - Google Patents
使用亞甲基醌／烷基羥胺組合之乙烯基芳族單體的聚合物抑制 Download PDFInfo
- Publication number
- TWI461406B TWI461406B TW099101907A TW99101907A TWI461406B TW I461406 B TWI461406 B TW I461406B TW 099101907 A TW099101907 A TW 099101907A TW 99101907 A TW99101907 A TW 99101907A TW I461406 B TWI461406 B TW I461406B
- Authority
- TW
- Taiwan
- Prior art keywords
- inhibitor
- monomer
- retarder
- combination
- butyl
- Prior art date
Links
- 239000000178 monomer Substances 0.000 title claims description 29
- 229920002554 vinyl polymer Polymers 0.000 title claims description 7
- 229920000642 polymer Polymers 0.000 title description 16
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 title 2
- 125000000217 alkyl group Chemical group 0.000 title 1
- 230000005764 inhibitory process Effects 0.000 title 1
- LGRLWUINFJPLSH-UHFFFAOYSA-N methanide Chemical compound [CH3-] LGRLWUINFJPLSH-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 claims description 51
- 238000000034 method Methods 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 13
- 238000006116 polymerization reaction Methods 0.000 claims description 13
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 10
- -1 7-substituted-methylene fluorenes Chemical class 0.000 claims description 7
- BJEMXPVDXFSROA-UHFFFAOYSA-N 3-butylbenzene-1,2-diol Chemical compound CCCCC1=CC=CC(O)=C1O BJEMXPVDXFSROA-UHFFFAOYSA-N 0.000 claims description 5
- 230000002028 premature Effects 0.000 claims description 5
- SZMBYKBVFJKLQB-UHFFFAOYSA-N 3-(hydroxyamino)propan-1-ol Chemical compound OCCCNO SZMBYKBVFJKLQB-UHFFFAOYSA-N 0.000 claims description 4
- 230000002401 inhibitory effect Effects 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- IRXXTOXNJURUHK-UHFFFAOYSA-N C(C)(C)(C)C1=CC2=CC3=CC(C(=CC3=C2C=C1)C(C)(C)C)=CC(=O)O Chemical compound C(C)(C)(C)C1=CC2=CC3=CC(C(=CC3=C2C=C1)C(C)(C)C)=CC(=O)O IRXXTOXNJURUHK-UHFFFAOYSA-N 0.000 claims description 3
- 229920001174 Diethylhydroxylamine Polymers 0.000 claims description 3
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 claims description 3
- 231100000252 nontoxic Toxicity 0.000 claims description 3
- 230000003000 nontoxic effect Effects 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 2
- 229920002223 polystyrene Polymers 0.000 claims description 2
- 238000012545 processing Methods 0.000 claims description 2
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical group 0.000 claims 1
- 239000000463 material Substances 0.000 description 8
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 6
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000006698 induction Effects 0.000 description 4
- 150000002923 oximes Chemical class 0.000 description 4
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- IDBOAVAEGRJRIZ-UHFFFAOYSA-N methylidenehydrazine Chemical compound NN=C IDBOAVAEGRJRIZ-UHFFFAOYSA-N 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- JCRIDWXIBSEOEG-UHFFFAOYSA-N 2,6-dinitrophenol Chemical compound OC1=C([N+]([O-])=O)C=CC=C1[N+]([O-])=O JCRIDWXIBSEOEG-UHFFFAOYSA-N 0.000 description 1
- QHJIRTVISXHLRI-UHFFFAOYSA-N 6-methyl-4,6-dinitrocyclohexa-1,3-dien-1-ol Chemical compound [O-][N+](=O)C1(C)CC([N+]([O-])=O)=CC=C1O QHJIRTVISXHLRI-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/38—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation
- C08F2/40—Polymerisation using regulators, e.g. chain terminating agents, e.g. telomerisation using retarding agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C7/00—Purification; Separation; Use of additives
- C07C7/20—Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F12/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F12/02—Monomers containing only one unsaturated aliphatic radical
- C08F12/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F12/06—Hydrocarbons
- C08F12/08—Styrene
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/06—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen
- C09K15/08—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing oxygen containing a phenol or quinone moiety
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Analytical Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Water Supply & Treatment (AREA)
- Materials Engineering (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/366,154 US7651635B1 (en) | 2009-02-05 | 2009-02-05 | Polymer inhibition of vinyl aromatic monomers using a quinone methide/alkyl hydroxylamine combination |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW201035046A TW201035046A (en) | 2010-10-01 |
| TWI461406B true TWI461406B (zh) | 2014-11-21 |
Family
ID=41559765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW099101907A TWI461406B (zh) | 2009-02-05 | 2010-01-25 | 使用亞甲基醌／烷基羥胺組合之乙烯基芳族單體的聚合物抑制 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7651635B1 (OSRAM) |
| EP (1) | EP2393765B1 (OSRAM) |
| JP (1) | JP5536106B2 (OSRAM) |
| KR (1) | KR101613760B1 (OSRAM) |
| CN (1) | CN102307830B (OSRAM) |
| BR (1) | BRPI1005420B1 (OSRAM) |
| CA (1) | CA2750187C (OSRAM) |
| ES (1) | ES2398053T3 (OSRAM) |
| SG (1) | SG173564A1 (OSRAM) |
| TW (1) | TWI461406B (OSRAM) |
| WO (1) | WO2010091040A1 (OSRAM) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8691994B2 (en) | 2011-02-03 | 2014-04-08 | Nalco Company | Multi-component polymerization inhibitors for ethylenically unsaturated monomers |
| US8884038B2 (en) * | 2011-06-13 | 2014-11-11 | Nalco Company | Synthesis of 7-acetyleno quinone methide derivatives and their application as vinylic polymerization retarders |
| US9090526B2 (en) * | 2011-06-13 | 2015-07-28 | Nalco Company | Synergistic combination for inhibiting polymerization of vinyl monomers |
| MX2014002218A (es) | 2011-08-26 | 2014-05-28 | Dorf Ketal Chemicals India Private Ltd | Composicion aditiva para el control y la inhibicion de la polimerizacion del estireno y metodo de preparacion y uso de la misma. |
| EP2788303B1 (en) * | 2011-12-09 | 2015-07-15 | Dorf Ketal Chemicals (India) Private Limited | Improved additives composition for control and inhibition of polymerization of aromatic vinyl monomers, and method of use thereof |
| MX339599B (es) * | 2011-12-26 | 2016-05-31 | Dorf Ketal Chemicals (India) Private Ltd | Composicion de aditivo a base de amina mejorada para el control y la inhibicion de la polimerizacion de monomeros de vinilo aromaticos, y metodo de uso de la misma. |
| JP6255405B2 (ja) * | 2012-08-24 | 2017-12-27 | ドルフ ケタール ケミカルズ （インディア）プライヴェート リミテッド | モノマーの重合の制御及び阻害用キノンメチド及びアミンの組成物、並びにその製造及び使用する方法 |
| US9611336B2 (en) * | 2012-10-25 | 2017-04-04 | Baker Hughes Incorporated | Quinone compounds for inhibiting monomer polymerization |
| US9944577B2 (en) | 2012-10-25 | 2018-04-17 | Baker Hughes, A Ge Company, Llc | Hydroquinone compounds for inhibiting monomer polymerization |
| IN2013MU01165A (OSRAM) * | 2013-03-26 | 2015-04-24 | Dorf Ketal Chemicals India Private Ltd | |
| US9399622B2 (en) | 2013-12-03 | 2016-07-26 | Ecolab Usa Inc. | Nitroxide hydroxylamine and phenylenediamine combinations as polymerization inhibitors for ethylenically unsaturated monomer processes |
| JP6530868B2 (ja) * | 2016-02-13 | 2019-06-12 | ドルフ ケタール ケミカルズ （インディア）プライヴェート リミテッド | ビニル芳香族モノマーの重合を制御及び阻害するための組成物及びその使用方法 |
| TW202005938A (zh) | 2018-07-13 | 2020-02-01 | 美商藝康美國公司 | 具有胺穩定劑之聚合抑制劑及阻滯劑組合物 |
| KR102763208B1 (ko) * | 2018-07-13 | 2025-02-04 | 에코랍 유에스에이 인코퍼레이티드 | 비닐계 단량체에 대한 항파울런트로서의 산소화 아민 및 퀴논 메티드의 조성물 |
| TWI880966B (zh) * | 2019-10-11 | 2025-04-21 | 美商藝康美國公司 | 醌甲基化物及銨鹽抗聚合劑組合物及方法 |
| WO2025217595A1 (en) * | 2024-04-12 | 2025-10-16 | Bl Technologies, Inc. | Boosted styrene polymerization retarder and method of use |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09176215A (ja) * | 1995-04-14 | 1997-07-08 | Ciba Geigy Ag | 不飽和モノマーのための阻害剤としての７−置換キノンメチド |
| US20040097619A1 (en) * | 2001-03-20 | 2004-05-20 | Troutman Malisa V. | Flame retardant compositions |
| CN1761638A (zh) * | 2003-03-17 | 2006-04-19 | 伯东株式会社 | 芳香族乙烯基化合物的聚合抑制剂以及聚合抑制方法 |
| US20060155140A1 (en) * | 2000-10-16 | 2006-07-13 | Uniroyal Chemical Company, Inc A Corporation Of The State Of Delaware | Blends of quinone alkide and nitroxyl compounds as polymerization inhibitors |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3390198A (en) * | 1965-12-16 | 1968-06-25 | Koppers Co Inc | Tertiary-butyl-5-methyl catechol as polymerization inhibitor for hot styrene |
| US4003800A (en) | 1976-01-02 | 1977-01-18 | Gulf Research & Development Company | Styrene purification process |
| US4409408A (en) * | 1982-09-24 | 1983-10-11 | Atlantic Richfield Company | Inhibiting polymerization of vinyl aromatic monomers |
| IT1245845B (it) * | 1990-09-17 | 1994-10-25 | Montedipe Srl | Processo per la depurazione di un monomero vinilaromatico. |
| US5446220A (en) | 1994-08-24 | 1995-08-29 | Betz Laboratories, Inc. | Methods for inhibiting vinyl aromatic monomer polymerization |
| US6024894A (en) | 1998-03-25 | 2000-02-15 | Betzdearborn Inc. | Compositions and methods for inhibiting vinyl aromatic monomer polymerization |
| US6685823B2 (en) * | 2000-10-16 | 2004-02-03 | Uniroyal Chemical Company, Inc. | C-nitrosoaniline compounds and their blends as polymerization inhibitors |
| US6960279B2 (en) * | 2002-05-06 | 2005-11-01 | Fina Technology, Inc. | Method for stabilizing vinyl aromatic monomers using selected polymerization inhibitors and polymers prepared therewith |
-
2009
- 2009-02-05 US US12/366,154 patent/US7651635B1/en active Active
-
2010
- 2010-01-25 TW TW099101907A patent/TWI461406B/zh active
- 2010-02-03 BR BRPI1005420-0A patent/BRPI1005420B1/pt active IP Right Grant
- 2010-02-03 CN CN201080006847.0A patent/CN102307830B/zh active Active
- 2010-02-03 ES ES10704042T patent/ES2398053T3/es active Active
- 2010-02-03 SG SG2011056546A patent/SG173564A1/en unknown
- 2010-02-03 WO PCT/US2010/022977 patent/WO2010091040A1/en not_active Ceased
- 2010-02-03 JP JP2011549218A patent/JP5536106B2/ja active Active
- 2010-02-03 EP EP10704042A patent/EP2393765B1/en active Active
- 2010-02-03 KR KR1020117018201A patent/KR101613760B1/ko active Active
- 2010-02-03 CA CA2750187A patent/CA2750187C/en active Active
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH09176215A (ja) * | 1995-04-14 | 1997-07-08 | Ciba Geigy Ag | 不飽和モノマーのための阻害剤としての７−置換キノンメチド |
| US20060155140A1 (en) * | 2000-10-16 | 2006-07-13 | Uniroyal Chemical Company, Inc A Corporation Of The State Of Delaware | Blends of quinone alkide and nitroxyl compounds as polymerization inhibitors |
| US20040097619A1 (en) * | 2001-03-20 | 2004-05-20 | Troutman Malisa V. | Flame retardant compositions |
| CN1761638A (zh) * | 2003-03-17 | 2006-04-19 | 伯东株式会社 | 芳香族乙烯基化合物的聚合抑制剂以及聚合抑制方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102307830B (zh) | 2014-10-22 |
| KR20110122111A (ko) | 2011-11-09 |
| CA2750187C (en) | 2016-05-10 |
| EP2393765B1 (en) | 2012-12-26 |
| JP2012516933A (ja) | 2012-07-26 |
| BRPI1005420B1 (pt) | 2021-05-11 |
| ES2398053T3 (es) | 2013-03-13 |
| TW201035046A (en) | 2010-10-01 |
| KR101613760B1 (ko) | 2016-04-19 |
| JP5536106B2 (ja) | 2014-07-02 |
| BRPI1005420A2 (pt) | 2020-08-18 |
| CA2750187A1 (en) | 2010-08-12 |
| EP2393765A1 (en) | 2011-12-14 |
| WO2010091040A1 (en) | 2010-08-12 |
| US7651635B1 (en) | 2010-01-26 |
| CN102307830A (zh) | 2012-01-04 |
| SG173564A1 (en) | 2011-09-29 |
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