GB827511A - Improvements in or relating to methyl ethyl ketone peroxides - Google Patents
Improvements in or relating to methyl ethyl ketone peroxidesInfo
- Publication number
- GB827511A GB827511A GB424457A GB424457A GB827511A GB 827511 A GB827511 A GB 827511A GB 424457 A GB424457 A GB 424457A GB 424457 A GB424457 A GB 424457A GB 827511 A GB827511 A GB 827511A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl ethyl
- ethyl ketone
- peroxides
- acid
- dimethyl phthalate
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C407/00—Preparation of peroxy compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Abstract
Peroxides of methyl ethyl ketone are prepared by contacting methyl ethyl ketone with aqueous hydrogen peroxide in the presence of an inert diluent, the hydrogen ion concentration being in the range 10-7 gm. ions/litre to that which would be provided by an acid of dissociation constant 2 x 10-2 at 18 DEG C. when present in the reaction mixture to the extent of 5% by weight. Preferably 80-90% w/w. hydrogen peroxide is used; the inert diluent is preferably dimethyl phthalate and the temperature is preferably not allowed to rise above 30 DEG C. Preferably an acid catalyst is present, which may be a dilute mineral or organic acid or an ion exchange resin in the acid form. Preferably where an acid substance is used, the reaction product is either incompletely washed to a pH of 5 to 6.5 or washed with a pH 5 to 6.5 buffer. When washing with an unbuffered solution, a dilute electrolyte solution is preferably used to avoid emulsion formation. In a preferred embodiment, methyl ethyl ketone is added slowly with agitation and cooling to a mixture containing dimethyl phthalate and hydrogen peroxide, followed by washing and drying after the product has formed. Examples describe the preparation of solutions of peroxides of methyl ethyl ketone in dimethyl phthalate using no catalyst or acetic or phosphoric acids, and the washing of the product with dilute aqueous sodium sulphate. The products are useful as polymerization initiators.ALSO:Peroxides of methyl ethyl ketone (for preparation see Group IV (b)) are used in conjunction with activators such as cobalt naphthenate in the polymerization of thermosetting resins, such as unsaturated polyesters, with styrene or similar cross-linking monomers. The peroxides may be in an inert diluent such as dimethyl phthalate and have higher activity giving a quicker gel time.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB424457A GB827511A (en) | 1957-02-07 | 1957-02-07 | Improvements in or relating to methyl ethyl ketone peroxides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB424457A GB827511A (en) | 1957-02-07 | 1957-02-07 | Improvements in or relating to methyl ethyl ketone peroxides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB827511A true GB827511A (en) | 1960-02-03 |
Family
ID=9773449
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB424457A Expired GB827511A (en) | 1957-02-07 | 1957-02-07 | Improvements in or relating to methyl ethyl ketone peroxides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB827511A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3428689A (en) * | 1963-09-21 | 1969-02-18 | Laporte Chemical | Peroxy compounds |
US3507800A (en) * | 1966-10-05 | 1970-04-21 | U S Peroxygen Corp | Flame resistant peroxides |
US3668139A (en) * | 1968-12-10 | 1972-06-06 | Grace W R & Co | Catalyst and method of polyester polymerization |
JPS4925644B1 (en) * | 1970-07-07 | 1974-07-02 | ||
JPS4925645B1 (en) * | 1970-08-08 | 1974-07-02 | ||
US5808110A (en) * | 1994-07-21 | 1998-09-15 | Akzo Nobel Nv | Cyclic ketone peroxide formulations |
WO2000073267A1 (en) * | 1999-05-27 | 2000-12-07 | Crompton Corporation | Heteropolyacids as catalysts for a synthesis of ketone peroxides |
WO2004076405A1 (en) * | 2003-02-28 | 2004-09-10 | Degussa Initiators Gmbh & Co. Kg | Method for the production of trimeric ketone peroxide solutions |
-
1957
- 1957-02-07 GB GB424457A patent/GB827511A/en not_active Expired
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3428689A (en) * | 1963-09-21 | 1969-02-18 | Laporte Chemical | Peroxy compounds |
US3507800A (en) * | 1966-10-05 | 1970-04-21 | U S Peroxygen Corp | Flame resistant peroxides |
US3668139A (en) * | 1968-12-10 | 1972-06-06 | Grace W R & Co | Catalyst and method of polyester polymerization |
JPS4925644B1 (en) * | 1970-07-07 | 1974-07-02 | ||
JPS4925645B1 (en) * | 1970-08-08 | 1974-07-02 | ||
US5808110A (en) * | 1994-07-21 | 1998-09-15 | Akzo Nobel Nv | Cyclic ketone peroxide formulations |
WO2000073267A1 (en) * | 1999-05-27 | 2000-12-07 | Crompton Corporation | Heteropolyacids as catalysts for a synthesis of ketone peroxides |
WO2004076405A1 (en) * | 2003-02-28 | 2004-09-10 | Degussa Initiators Gmbh & Co. Kg | Method for the production of trimeric ketone peroxide solutions |
JP2006519203A (en) * | 2003-02-28 | 2006-08-24 | デグサ イニシエータース ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディートゲゼルシャフト | Method for producing a solution of ketone peroxide trimer |
US7247754B2 (en) | 2003-02-28 | 2007-07-24 | Degussa Initiators Gmbh & Co. Kg. | Method for the production of trimeric ketone peroxide solutions |
JP4723475B2 (en) * | 2003-02-28 | 2011-07-13 | デグサ イニシエータース ゲゼルシャフト ミット ベシュレンクテル ハフツング ウント コンパニー コマンディートゲゼルシャフト | Method for producing a solution of ketone peroxide trimer |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB630286A (en) | Manufacture of peroxides | |
GB827511A (en) | Improvements in or relating to methyl ethyl ketone peroxides | |
GB1094315A (en) | Improvements in or relating to a process for preparing expandable plastic particles | |
GB1425307A (en) | Process for the production of polyactones derived from poly- alpha-hydroxyacrylic acids | |
ES8200337A1 (en) | Process for the production of percarboxylic acids. | |
ATE30717T1 (en) | PROCESS FOR THE PRODUCTION OF WATER-INSOLUBLE PEROXYCARBONIC ACIDS. | |
GB961960A (en) | Novel derivatives of trimellitic anhydride | |
ATE875T1 (en) | PROCESS FOR THE PRODUCTION OF AROMATIC POXYCARBONIC ACIDS. | |
GB899413A (en) | Improvements in polymerization | |
GB1050841A (en) | ||
US2118863A (en) | Mixed polymerization products | |
GB976570A (en) | Amphoteric ion exchange resins | |
GB912061A (en) | Improvements in or relating to the manufacture of ketone peroxides | |
CN111454205B (en) | Method for synthesizing pyridine-N-oxide by catalytic oxidation through continuous non-solvent method | |
GB873614A (en) | Improvements in or relating to the production of substituted cyclohexanone peroxides | |
GB912268A (en) | Process for the polymerisation of unsaturated monomeric organic compounds in aqueous emulsion | |
GB821092A (en) | Improvements in or relating to the manufacture of polyvinyl acetals | |
US2511498A (en) | Rubber impregnated fabrics | |
GB795889A (en) | Preparation of peracetic acid | |
GB956115A (en) | Improvements in or relating to a process for the preparation of organic peroxides | |
ES447413A1 (en) | Process for the preparation of perpropionic acid solutions | |
GB905877A (en) | A process for the production of dibasic organic di-per carboxylic acids | |
SU149420A1 (en) | The method of obtaining epoxycyclododecadiene-5,9 | |
GB896803A (en) | Process for the manufacture of water-insoluble quinacridones free from sulphonic acid groups | |
GB959514A (en) | New cation exchange resins |