Samuel Joseph , Fredah Batale Abifarin , Williams Wangka Jikisim , Bekas Nabieyeh Jibrillu , Johnson Kehinde Abifarin
{"title":"Sustainable synthesis of shea butter-derived bio-lubricants: A green alternative to mineral oils","authors":"Samuel Joseph , Fredah Batale Abifarin , Williams Wangka Jikisim , Bekas Nabieyeh Jibrillu , Johnson Kehinde Abifarin","doi":"10.1016/j.nxsust.2025.100128","DOIUrl":null,"url":null,"abstract":"<div><div>As environmental concerns over mineral oil-based lubricants rise, the search for sustainable alternatives intensifies. This study explores producing bio-lubricant from shea butter using double-transesterification with sodium hydroxide and tetraoxosulphate (IV) acid as catalysts. The process achieved a 57.89 % yield at a 4:1 molar ratio of shea methyl ester to trimethylolpropane, with 0.8 % w/w catalyst at 110°C for three hours. Fourier-transform infrared (FTIR) spectroscopy identified key functional groups in the crude oil: O-H (3340 cm⁻¹), C-H (2914–2980 cm⁻¹), C<img>O (1740 cm⁻¹), and C-H terminal alkane bonds (1456 cm⁻¹). In the bio-lubricant, the spectrum showed C-O ester groups (1173–1253 cm⁻¹), C<img>O carbonyl groups (1740 cm⁻¹), C-H stretching (2855–2923 cm⁻¹), and O-H polyol groups (3356 cm⁻¹). These findings demonstrate significant chemical and physicochemical modifications, underscoring the potential of shea butter-based bio-lubricant as a sustainable and green alternative to mineral oils.</div></div>","PeriodicalId":100960,"journal":{"name":"Next Sustainability","volume":"5 ","pages":"Article 100128"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Next Sustainability","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2949823625000315","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
As environmental concerns over mineral oil-based lubricants rise, the search for sustainable alternatives intensifies. This study explores producing bio-lubricant from shea butter using double-transesterification with sodium hydroxide and tetraoxosulphate (IV) acid as catalysts. The process achieved a 57.89 % yield at a 4:1 molar ratio of shea methyl ester to trimethylolpropane, with 0.8 % w/w catalyst at 110°C for three hours. Fourier-transform infrared (FTIR) spectroscopy identified key functional groups in the crude oil: O-H (3340 cm⁻¹), C-H (2914–2980 cm⁻¹), CO (1740 cm⁻¹), and C-H terminal alkane bonds (1456 cm⁻¹). In the bio-lubricant, the spectrum showed C-O ester groups (1173–1253 cm⁻¹), CO carbonyl groups (1740 cm⁻¹), C-H stretching (2855–2923 cm⁻¹), and O-H polyol groups (3356 cm⁻¹). These findings demonstrate significant chemical and physicochemical modifications, underscoring the potential of shea butter-based bio-lubricant as a sustainable and green alternative to mineral oils.