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PublicationIndustrial Crops and Products
Year2018
Volume116
Pages90-96
International

Enzymatic esterification of palm fatty acids distillate for the production of polyolesters with biolubricant properties

Authors:Roberto Fernandez-Lafuente
Groups of research:Optimization of biocatalysts and bioprocesses
Keysson Vieira Fernandes1, Aikaterini Papadaki2, José André da Silva Cavalcanti3, Roberto Fernandez-Lafuente4, Apostolis A. Koutinas2*, Denise Maria Guimarães Freire1*
 
1 Department of Biochemistry, Institute of Chemistry, Federal University of Rio de Janeiro, Cidade Universitária, Centro de Tecnologia, BL A, SL 549, Ilha do Fundão, 21949-900, Rio de Janeiro, Brazil.
2 Department of Food Science and Human Nutrition, Agricultural University of Athens, Iera Odos 75, 118 55, Athens, Greece.
3 Cenpes, Centro de Pesquisas Leopoldo Américo Miguez de Mello, Petrobras, Rio de Janeiro, Brazil.
4 Departamento de Biocatálisis. ICP-CSIC. C/ Marie Curie 2. Campus UAM-CSIC. Cantoblanco, 28049 Madrid, Spain.



This contribution describes a sustainable, environmentally benign process for the production of biolubricants. The reaction was performed in a solvent-free system using a side stream from palm-oil refining (palm fatty-acid distillate, PFAD) and polyols as substrates for enzymatic catalysis. Biocatalysts consume less energy than chemical processes, and produce esters with good lubricant properties and environmentally friendly characteristics such as high biodegradability and low toxicity. The effects of different parameters (molar ratio, temperature and enzyme concentration) were evaluated during esterification of PFAD with neopentyl glycol (NPG) or trimethylolpropane (TMP) to produce polyol esters. The products obtained through esterification of PFAD with NPG and TMP in the stoichiometric molar ratio at 45 °C, using 4% (w/w) of Candida rugosa lipase, attained a modification of around 90% of hydroxyl groups (OH) at 10 and 8 h, respectively. These conditions were used to reach the maximum OH esterification for PFAD-TMP esters (94%) and PFAD-DIP esters (87%). NMR analysis of the final ester composition showed that the PFAD-TMP and PFAD-DIP esters were composed mostly of triesters and diesters, respectively. The properties of these esters were also characterized, including fusion and crystallization temperatures, viscosity, pour point and oxidative stability. The polyol esters showed promising lubricant properties, such as oxidative stability  and viscositywithin the acceptable range for many applications. This study demonstrated the potential of using PFAD for the production of environmentally benign polyol esters through non-conventional catalysis.
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