GB741492A - Process for the manufacture of plasticizers - Google Patents
Process for the manufacture of plasticizersInfo
- Publication number
- GB741492A GB741492A GB9298/53A GB929853A GB741492A GB 741492 A GB741492 A GB 741492A GB 9298/53 A GB9298/53 A GB 9298/53A GB 929853 A GB929853 A GB 929853A GB 741492 A GB741492 A GB 741492A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acids
- acid
- mono
- poly
- oleyl
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
- C08K5/101—Esters; Ether-esters of monocarboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Plasticizers for vinyl resins and cellulose derivatives are made by epoxidizing an oleic acid ester of a mono- or poly-hydric alcohol or an oleyl alcohol ester of a mono- or poly-basic carboxylic acid and treating the resultant epoxide, optionally in the presence of an esterification catalyst with a mono- or poly-basic carboxylic acid or its anhydride (see Group IV (b)). In examples, oleyl butyrate is epoxidized with hydrogen peroxide in the presence of formic acid and esterified with (1) butyric, (2) benzoic, and (6) adipic acids; in (3), (4) and (5) mixed lower paraffin oxidation fatty acids (acid No. 480) are used to esterify respectively epoxides obtained from butyl oleate with performic acid, oleyl oleate with hydrogen peroxide and formic acid and dioleyl phthalate, the products of (1), (2), (5) and (6) being compatible with polyvinyl chloride, e.g. 1-5 times as much resin as ester may be used, of (2) and (4) with nitrocellulose, of (3) with mixed styrenebutadiene resins and of (4) with benzyl cellulose.ALSO:Ester plasticizers are made by epoxidizing an oleic acid ester of a mono- or poly-hydric alcohol or an oleyl alcohol ester of a mono- or poly-basic carboxylic acid and treating the resultant epoxide, optionally in the presence of an esterification catalyst, with a mono- or poly-basic carboxylic acid or its anhydride. Epoxidizing is effected with organic per-acids or hydrogen peroxide in the presence of carboxylic acids. In the second stage the epoxide is esterified, at least 2 mols. of a mono- or one mol. of a di-basic acid being required per mol. of epoxide, reaction temperatures may exceed 200 DEG C. and water formed should be removed. Specified alcohols are ethanol, butanol, cyclohexanol, octanol, 2-ethyl hexanol, dodecanol, stearyl and oleyl alcohol, mixtures of lower alcohols obtainable by reduction of acids made by oxidizing paraffins, mixtures of oxo alcohols made from olefines, mixtures of guerbet alcohols, butoxy - ethanol, 6 - chloro - hexanol, tetrahydro-furfuryl alcohol, benzyl alcohol, phenyl and phenoxy ethanol, glycol, 1,4-butandiol, 1,4-hexandiol, diglycol, glycerol, trimethylol ethane, pentaerythritol and dipentaerythritol. Specified acids for the epoxidizing reaction are acetic, butyric, caproic, lauric, stearic and oleic acid, mixtures of C4-11 paraffin oxidation acids, butoxy-, octyl-, phenyl- and phenoxy-acetic acids, benzoic, naphthoic, succinic, maleic, adipic, sebacic, diglycollic, phthalic and terephthalic acids. Anhydrides of these acids may be used in the second stage. In examples oleyl butyrate is epoxdized with hydrogen peroxide in the presence of formic acid and esterified with (1) butyric, (2) benzoic and (6) adipic acids, in (3), (4) and (5) mixed lower paraffin oxidation fatty acids (acid No. 480) are used to esterify respectively epoxides obtained from butyl oleate with performic acid, oleyl oleate with hydrogen peroxide and formic acid and dioleyl phthalate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE741492X | 1952-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB741492A true GB741492A (en) | 1955-12-07 |
Family
ID=6644822
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9298/53A Expired GB741492A (en) | 1952-04-09 | 1953-04-07 | Process for the manufacture of plasticizers |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB741492A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990002722A1 (en) * | 1988-09-01 | 1990-03-22 | Henkel Kommanditgesellschaft Auf Aktien | Process for producing fatty alcohol derivatives |
WO2014130391A1 (en) * | 2013-02-25 | 2014-08-28 | Arkema Inc. | Unsaturated fatty acid ester-based plastic additives |
-
1953
- 1953-04-07 GB GB9298/53A patent/GB741492A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1990002722A1 (en) * | 1988-09-01 | 1990-03-22 | Henkel Kommanditgesellschaft Auf Aktien | Process for producing fatty alcohol derivatives |
EP0361080A1 (en) * | 1988-09-01 | 1990-04-04 | Henkel Kommanditgesellschaft auf Aktien | Process for the preparation of fatty alcohol derivatives |
WO2014130391A1 (en) * | 2013-02-25 | 2014-08-28 | Arkema Inc. | Unsaturated fatty acid ester-based plastic additives |
US9586918B2 (en) | 2013-02-25 | 2017-03-07 | Arkema Inc. | Unsaturated fatty acid ester-based compositions useful as plastic additives |
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