Rice bran oil biorefining: functionalization with acrylate

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Edgar David Ponciano Leyva https://orcid.org/0000-0002-4505-6038
Jacqueline Zúñiga Díaz https://orcid.org/0000-0003-4201-6476
Jesús Porcayo Calderón https://orcid.org/0000-0002-6943-3926
Francisco Javier Hernández Campos https://orcid.org/0000-0001-7604-6169
José Elias Salado Huerta https://orcid.org/0000-0001-5597-7511
Macdiel Emilio Acevedo Quiroz https://orcid.org/0000-0003-0017-6535
Alfredo Quinto Hernández https://orcid.org/0000-0003-0049-6539

Keywords

Acrylation, Epoxidation, Biorefining

Resumen

Objective: To obtain acrylated refined rice bran oil (RBO) using a combined functionalization: first,
epoxidation with H2O2/Novozym 435 lipase, followed by acrylate group insertion.
Design/Methodology/Approach: After being epoxidized with H2O2/Novozym 435, the refined rice bran
oil was acrylated via epoxy ring-opening, using triethanolamine as catalyst and 4-methoxyphenol as inhibitor.
The experimental conditions of temperature (T=100 and 110 °C) and reaction time (t=3 and 4 hours), as well
as the ratio of g eRBO (epoxidized oil) to g acrylic acid (1.5 and 2.0) were considered for the functionalization.
The functionalizations were monitored using iodine value (IV), saponification value (SV), and oxirane oxygen
content (OOC), Fourier transform infrared (FTIR), and nuclear magnetic resonance (1H NMR), which allowed
the estimation of the %Acrylation.
Results: The 1H NMR studies indicate that the acrylation of rice bran oil is efficient, which is confirmed with
the evolution of IV, SV, and OOC. Using the OOC, the best acrylation condition was identified at T=110
°C, t=3 hours, and ratio of g eRBO to g acrylic acid=1.5, obtaining a %Acrylation of 85.89% via 1H NMR.
Study Limitations/Implications: Partially acrylated rice bran oil may become an intermediate in the
biorefining of this oil and be used in the synthesis of crosslinked polymers.
Findings/Conclusions: Refined rice bran oil was efficiently acrylated using two consecutive steps: it was
initially epoxidized with H2O2/Novozym 435, followed by functionalization with acrylate group.

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