GB1433400A - Method of inhibiting the polymersation of acrylic acid or its esters - Google Patents
Method of inhibiting the polymersation of acrylic acid or its estersInfo
- Publication number
- GB1433400A GB1433400A GB5762473A GB5762473A GB1433400A GB 1433400 A GB1433400 A GB 1433400A GB 5762473 A GB5762473 A GB 5762473A GB 5762473 A GB5762473 A GB 5762473A GB 1433400 A GB1433400 A GB 1433400A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acrylic acid
- copper
- inhibiting
- dec
- compound selected
- 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
Links
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 title abstract 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title abstract 4
- 230000002401 inhibitory effect Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 150000002148 esters Chemical class 0.000 title 1
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 abstract 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract 2
- 125000005396 acrylic acid ester group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 abstract 2
- 238000004821 distillation Methods 0.000 abstract 2
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 abstract 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 abstract 1
- BJEMXPVDXFSROA-UHFFFAOYSA-N 3-butylbenzene-1,2-diol Chemical compound CCCCC1=CC=CC(O)=C1O BJEMXPVDXFSROA-UHFFFAOYSA-N 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- CMRVDFLZXRTMTH-UHFFFAOYSA-L copper;2-carboxyphenolate Chemical compound [Cu+2].OC1=CC=CC=C1C([O-])=O.OC1=CC=CC=C1C([O-])=O CMRVDFLZXRTMTH-UHFFFAOYSA-L 0.000 abstract 1
- IXPUJMULXNNEHS-UHFFFAOYSA-L copper;n,n-dibutylcarbamodithioate Chemical compound [Cu+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC IXPUJMULXNNEHS-UHFFFAOYSA-L 0.000 abstract 1
- OBBCYCYCTJQCCK-UHFFFAOYSA-L copper;n,n-diethylcarbamodithioate Chemical compound [Cu+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S OBBCYCYCTJQCCK-UHFFFAOYSA-L 0.000 abstract 1
- ZOUQIAGHKFLHIA-UHFFFAOYSA-L copper;n,n-dimethylcarbamodithioate Chemical compound [Cu+2].CN(C)C([S-])=S.CN(C)C([S-])=S ZOUQIAGHKFLHIA-UHFFFAOYSA-L 0.000 abstract 1
- 150000001896 cresols Chemical class 0.000 abstract 1
- 229910001882 dioxygen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 229960000907 methylthioninium chloride Drugs 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 229950000688 phenothiazine Drugs 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 abstract 1
- 239000012808 vapor phase Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/487—Separation; Purification; Stabilisation; Use of additives by treatment giving rise to chemical modification
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D3/00—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping
- B01D3/34—Distillation or related exchange processes in which liquids are contacted with gaseous media, e.g. stripping with one or more auxiliary substances
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/43—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
- C07C51/44—Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/42—Separation; Purification; Stabilisation; Use of additives
- C07C51/50—Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/48—Separation; Purification; Stabilisation; Use of additives
- C07C67/62—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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12818472A JPS5234606B2 (enrdf_load_stackoverflow) | 1972-12-22 | 1972-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1433400A true GB1433400A (en) | 1976-04-28 |
Family
ID=14978499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5762473A Expired GB1433400A (en) | 1972-12-22 | 1973-12-12 | Method of inhibiting the polymersation of acrylic acid or its esters |
Country Status (10)
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2931553A1 (de) * | 1979-08-03 | 1981-02-26 | Basf Ag | Verfahren zur stabilisierung monomerer acrylsaeureester gegen vorzeitige polymerisation |
| JPS57197684U (enrdf_load_stackoverflow) * | 1981-06-11 | 1982-12-15 | ||
| US4915873A (en) * | 1988-01-22 | 1990-04-10 | Uniroyal Chemical Company, Inc. | Polymerization inhibitor composition for vinyl aromatic compounds |
| ES2077811T3 (es) * | 1990-11-09 | 1995-12-01 | Nippon Catalytic Chem Ind | Inhibidor de polimerizacion y metodo de inhibicion de polimerizacion para un compuesto de vinilo. |
| JP2001081050A (ja) * | 1999-09-10 | 2001-03-27 | Nippon Shokubai Co Ltd | 易重合性化合物の取り扱い装置および取り扱い方法 |
| JP2005179352A (ja) * | 2003-11-28 | 2005-07-07 | Mitsubishi Chemicals Corp | （メタ）アクリル酸の精製方法 |
| CN1305832C (zh) * | 2003-11-28 | 2007-03-21 | 三菱化学株式会社 | (甲基)丙烯酸的提纯方法 |
| DE102010042216A1 (de) * | 2010-10-08 | 2011-06-09 | Basf Se | Verfahren zur Hemmung der unerwünschten radikalischen Polymerisation von in einer flüssigen Phase P befindlicher Acrylsäure |
| JP7204980B1 (ja) * | 2022-04-18 | 2023-01-16 | 信越化学工業株式会社 | 水酸基および（メタ）アクリル基含有シロキサンの精製方法、並びに、水酸基および（メタ）アクリル基含有シロキサン組成物 |
-
1972
- 1972-12-22 JP JP12818472A patent/JPS5234606B2/ja not_active Expired
-
1973
- 1973-12-12 GB GB5762473A patent/GB1433400A/en not_active Expired
- 1973-12-18 BE BE138988A patent/BE808771A/xx not_active IP Right Cessation
- 1973-12-18 NL NL7317334A patent/NL160802C/xx not_active IP Right Cessation
- 1973-12-20 BR BR1001573A patent/BR7310015D0/pt unknown
- 1973-12-21 FR FR7345893A patent/FR2211440B1/fr not_active Expired
- 1973-12-21 IT IT7081573A patent/IT1000592B/it active
- 1973-12-21 PL PL16756273A patent/PL94830B1/pl unknown
- 1973-12-21 CA CA188,746A patent/CA1013705A/en not_active Expired
- 1973-12-22 CS CS896873A patent/CS171189B2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL160802B (nl) | 1979-07-16 |
| DE2362373A1 (de) | 1974-07-11 |
| NL7317334A (enrdf_load_stackoverflow) | 1974-06-25 |
| AU6353073A (en) | 1975-06-12 |
| NL160802C (nl) | 1979-12-17 |
| BR7310015D0 (pt) | 1974-08-29 |
| JPS4985016A (enrdf_load_stackoverflow) | 1974-08-15 |
| BE808771A (fr) | 1974-04-16 |
| JPS5234606B2 (enrdf_load_stackoverflow) | 1977-09-05 |
| DE2362373B2 (de) | 1977-06-02 |
| FR2211440B1 (enrdf_load_stackoverflow) | 1976-10-08 |
| CA1013705A (en) | 1977-07-12 |
| CS171189B2 (enrdf_load_stackoverflow) | 1976-10-29 |
| FR2211440A1 (enrdf_load_stackoverflow) | 1974-07-19 |
| IT1000592B (it) | 1976-04-10 |
| PL94830B1 (pl) | 1977-08-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19931211 |