Use of heterogeneous acid catalysts based on mixed metal salts to produce biodiesel
US-2017283723-A1 · Oct 5, 2017 · US
US11767481B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11767481-B2 |
| Application number | US-202217888698-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 16, 2022 |
| Priority date | Aug 16, 2021 |
| Publication date | Sep 26, 2023 |
| Grant date | Sep 26, 2023 |
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The present invention concerns a process for producing biodiesel with bifunctional heterogeneous acidic catalysts from acidic raw materials, such as fatty acids and mixtures of fatty acids with triglycerides.
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The invention claimed is: 1. A process for producing biodiesel from acidic raw materials, characterized in that it comprises: a) the use of acidic raw materials and triglycerides in the biodiesel production process; b) the integration of the esterification step via acidic and heterogeneous catalysis with the treatment of oils and fats by physical refining and transesterification for the production of biodiesel; c) the use of three integration points: at the inlet of a first transesterification reactor, at the inlet of a second transesterification reactor and at the inlet of the washing process of the product of the transesterification section; d) use of a fixed bed reactor to carry out the esterification step via heterogeneous catalysis; e) a transesterification reaction system consisting of three continuous stirred tank reactors in series; f) sending the glycerin to a rectifying tower, while the methyl ester is dried and rectified to produce biodiesel; and g) the methanol-rich stream is rectified to be recycled. 2. The process according to claim 1 , characterized in that the raw material consists of free fatty acids with 85% to 90% m/m and triglycerides with 10 to 15% m/m. 3. The process according to claim 1 , characterized in that the heterogeneous solid acidic catalysts are bifunctional, having activity for esterification and transesterification. 4. The process according to claim 1 , characterized in that the esterification reaction is carried out at a temperature of 150 to 230° C., pressure of 10 to 25 bar (1 to 2.5 MPa), space velocity of 0.18 at 0.45 h −1 , methanol/raw material molar ratio ranging from 3.0 to 9.0. 5. The process according to claim 1 , characterized in that the transesterification reaction is carried out at the temperature of 55 to 65° C., pressure of 1 to 3bar (0.1 to 0.3 MPa), contact time of 60 to 120 minutes, methanol/raw material molar ratio ranging from 2.0 to 3.0.
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