Yayın:
Improved sustainable ionic liquid catalyzed production of symmetrical and non-symmetrical biological wax monoesters

dc.contributor.buuauthorYıldırım, Ayhan
dc.contributor.buuauthorMudaber, Sebghatullah
dc.contributor.buuauthorÖztürk, Serkan
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.contributor.researcheridW-8924-2019
dc.contributor.scopusid23101773900
dc.contributor.scopusid57203330328
dc.contributor.scopusid36452415600
dc.contributor.scopusid57212021331
dc.date.accessioned2024-01-10T06:19:22Z
dc.date.available2024-01-10T06:19:22Z
dc.date.issued2019-02
dc.description.abstractBiological wax esters are important commercial products used in various industrial and medicinal fields. These valuable compounds can be synthesized via several chemical and enzymatic reactions which have some advantages and more disadvantages. In particular, many strong acid catalysts cause undesirable structural changes in unsaturated fatty acids molecules. In the present study, easily accessible 1-hexadecyl-3-sulfoimidazolium chloride as an ionic liquid is screened as a mild Bronsted acid metal free catalyst for the chemical esterification, or transesterification, of equimolar amounts of long chain fatty acids or fatty acid methyl esters, respectively, with fatty alcohols in a solventless medium. The various parameters affecting the yield of the wax ester are optimized, catalyst reuse studies, and large scale synthesis are also carried out. According to this alternative practical and green process, a series of wax esters (17 examples) are produced readily in good to excellent yields. There is no undesirable geometric cis-trans isomerization in unsaturated fatty acids under the reaction conditions used. The catalyst is also quite effective when triglycerides are converted directly to the wax esters via transesterification reaction. Practical Applications: With an effortless and environmentally friendly method developed in this study, various wax esters can be synthesized as valuable industrial materials. In order to synthesis these esters, there is not any restriction for starting compounds. The most important aspect of the developed procedures is that metallic or strong aggressive acidic catalysts are not used compared to existing procedures. It is possible to carry out large-scale syntheses of esters with high yields. In the present study, a series of industrial and medical important wax esters are synthesized from renewable sources in a solvent-free environment using IL-catalyzed environmentally friendly methods.
dc.identifier.citationYıldırım, A. vd. (2014). "Improved sustainable ionic liquid catalyzed production of symmetrical and non-symmetrical biological wax monoesters". European Journal of Lipid Science and Technology, 121(2), Article Number: 1800303.
dc.identifier.doi10.1002/ejlt.201800303
dc.identifier.issn1438-7697
dc.identifier.issn1438-9312
dc.identifier.issue2
dc.identifier.scopus2-s2.0-85058385479
dc.identifier.urihttps://doi.org/10.1002/ejlt.201800303
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/epdf/10.1002/ejlt.201800303
dc.identifier.urihttps://hdl.handle.net/11452/38918
dc.identifier.volume121
dc.identifier.wos000457583900005
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherWiley
dc.relation.journalEuropean Journal of Lipid Science and Technology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectEsters
dc.subjectTransesterification
dc.subjectFatty acids
dc.subjectAlcohols
dc.subjectGreen catalysis
dc.subjectWater
dc.subjectIonic liquids
dc.subjectEsters
dc.subjectTriglycerides
dc.subjectEnzymatic-synthesis
dc.subjectCarboxylic-acids
dc.subjectDehydration reactions
dc.subjectEfficient catalyst
dc.subjectDirect esterification
dc.subjectFatty-acids
dc.subjectFood science & technology
dc.subjectNutrition & dietetics
dc.subject.scopusCatalyst; Acetylation; Alcohol Derivative
dc.subject.wosFood science & technology
dc.subject.wosNutrition & dietetics
dc.titleImproved sustainable ionic liquid catalyzed production of symmetrical and non-symmetrical biological wax monoesters
dc.typeArticle
dc.wos.quartileQ2
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.atPubMed
local.indexed.atScopus

Dosyalar

Lisanslı seri

Şimdi gösteriliyor 1 - 1 / 1
Placeholder
Ad:
license.txt
Boyut:
1.71 KB
Format:
Item-specific license agreed upon to submission
Açıklama