2009
DOI: 10.1007/s11746-009-1455-7
|View full text |Cite
|
Sign up to set email alerts
|

The Influence of Reaction Parameters on the Epoxidation of Rapeseed Oil with Peracetic Acid

Abstract: The influence of reaction parameters on the epoxidation of rapeseed oil (RO) with peracetic acid obtained in situ from the reaction between 30 wt% hydrogen peroxide and glacial acetic acid (AA) has been studied. The course of the reaction was measured by changes of the iodine number (IN) and epoxy number (EN), used to estimate the degree of rapeseed oil conversion, yield, and the selectivity of transformation to epoxidized rapeseed oil in relation to the total amount of oil undergoing the transformation. The o… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
23
0
1

Year Published

2012
2012
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 34 publications
(24 citation statements)
references
References 15 publications
0
23
0
1
Order By: Relevance
“…The dominant constituents are (C18) fatty acids. The content of acids in the oil depends on some factors, i.e., type and origin of the oil, its freshness and the refining process [12].…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…The dominant constituents are (C18) fatty acids. The content of acids in the oil depends on some factors, i.e., type and origin of the oil, its freshness and the refining process [12].…”
Section: Introductionmentioning
confidence: 99%
“…It results in the formation of epoxy and acid reacting again with hydrogen peroxide. The presence of water, mineral and organic acids in the reaction medium is considered to be the main reason for decomposition of the epoxy groups due to hydrolysis or acylation [12]. Ring-opening reactions can be accompanied by oligomerization side reactions, which occur when the newly formed hydroxyl groups react with the existing epoxy groups, thus the selectivity of oil epoxidation rarely exceeds 80%.…”
Section: Introductionmentioning
confidence: 99%
“…Unsaturated compounds can be epoxidized economically; therefore, we converted the unsaturated bonds of cardanol esters into epoxy groups (Scheme ). Stoichiometric amounts of cardanol ester (0.2 mol) and formic acid (4.6 g, 0.1 mol) were introduced into a 250 mL flask.…”
Section: Methodsmentioning
confidence: 99%
“…Large scale conversion of vegetable oils to their corresponding epoxides is usually carried out using hydrogen peroxide and formic acid or acetic acid (16)(17)(18)(19). These conversions are highly exothermic, and therefore, pose inherent safety concerns.…”
Section: Epoxidationmentioning
confidence: 99%