Felipe Brondani Teixeira Ribas, Henrique Gasparetto, Nina Paula Gonçalves Salau
{"title":"乙醇和对花香烃混合物作为共溶剂萃取大豆油的传质研究:孔隙体积和表面扩散模型的早期应用","authors":"Felipe Brondani Teixeira Ribas, Henrique Gasparetto, Nina Paula Gonçalves Salau","doi":"10.1016/j.molliq.2025.127571","DOIUrl":null,"url":null,"abstract":"<div><div>Green solvents are widely explored for extracting oil from raw vegetable materials. As an alternative to hexane, ethanol is used in oil extraction but exhibits partial miscibility, requiring a co-solubilizer. p-Cymene, selected based on Hansen solubility parameter (<span><math><mrow><mi>HSP</mi></mrow></math></span>), enhances miscibility due to the reduced distance between solute and solvent, as indicated by the decrease in relative energy difference (<span><math><mrow><mi>RED</mi></mrow></math></span>). This study evaluated the pore volume and surface diffusion model (PVSDM) for vegetable oil extraction, with statistical results supporting its suitability. The best fits obtained were 0.990, 0.076, and 0.004 for <span><math><msup><mrow><mi>R</mi></mrow><mn>2</mn></msup></math></span>, <span><math><mrow><mi>SAE</mi></mrow></math></span>, and <span><math><mrow><mi>RMSE</mi></mrow></math></span>, respectively. The experimental data fit better to the PVSDM than the power-law models. While the So and MacDonald model fit more accurately, inconsistencies arose due to the non-stationary profile of the experimental data. Mechanistically, the PVSDM provided richer insights into mass transfer compared to the mass transfer kinetic model (MTKM). Extraction at 25 °C was influenced by the co-solvent addition, which may aid energy savings. <span><math><msup><mrow><mi>χ</mi></mrow><mn>2</mn></msup></math></span> and Fisher tests confirmed the model’s predictive accuracy. These findings are valuable for further exploration of soybean oil as a feedstock for food and biodiesel production.</div></div>","PeriodicalId":371,"journal":{"name":"Journal of Molecular Liquids","volume":"428 ","pages":"Article 127571"},"PeriodicalIF":5.3000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mass transfer study in soybean oil extraction using ethanol and mixtures with p-cymene as co-solvent: Early uses of pore volume and surface diffusion model\",\"authors\":\"Felipe Brondani Teixeira Ribas, Henrique Gasparetto, Nina Paula Gonçalves Salau\",\"doi\":\"10.1016/j.molliq.2025.127571\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Green solvents are widely explored for extracting oil from raw vegetable materials. As an alternative to hexane, ethanol is used in oil extraction but exhibits partial miscibility, requiring a co-solubilizer. p-Cymene, selected based on Hansen solubility parameter (<span><math><mrow><mi>HSP</mi></mrow></math></span>), enhances miscibility due to the reduced distance between solute and solvent, as indicated by the decrease in relative energy difference (<span><math><mrow><mi>RED</mi></mrow></math></span>). This study evaluated the pore volume and surface diffusion model (PVSDM) for vegetable oil extraction, with statistical results supporting its suitability. The best fits obtained were 0.990, 0.076, and 0.004 for <span><math><msup><mrow><mi>R</mi></mrow><mn>2</mn></msup></math></span>, <span><math><mrow><mi>SAE</mi></mrow></math></span>, and <span><math><mrow><mi>RMSE</mi></mrow></math></span>, respectively. The experimental data fit better to the PVSDM than the power-law models. While the So and MacDonald model fit more accurately, inconsistencies arose due to the non-stationary profile of the experimental data. Mechanistically, the PVSDM provided richer insights into mass transfer compared to the mass transfer kinetic model (MTKM). Extraction at 25 °C was influenced by the co-solvent addition, which may aid energy savings. <span><math><msup><mrow><mi>χ</mi></mrow><mn>2</mn></msup></math></span> and Fisher tests confirmed the model’s predictive accuracy. 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引用次数: 0
摘要
绿色溶剂被广泛用于从植物原料中萃取油脂。根据汉森溶解度参数(HSP)选择的对伞花烃,由于溶质和溶剂之间的距离缩短,相对能量差(RED)减小,因而提高了混溶性。本研究评估了用于植物油萃取的孔隙体积和表面扩散模型(PVSDM),统计结果支持其适用性。R2、SAE 和 RMSE 的最佳拟合值分别为 0.990、0.076 和 0.004。与幂律模型相比,实验数据与 PVSDM 的拟合效果更好。虽然 So 和 MacDonald 模型拟合得更准确,但由于实验数据的非稳态特征,出现了不一致的情况。从机理上讲,与传质动力学模型(MTKM)相比,PVSDM 对传质提供了更丰富的见解。25 °C 下的萃取受助溶剂添加量的影响,这可能有助于节能。这些发现对进一步探索大豆油作为食品和生物柴油生产原料的价值很高。
Mass transfer study in soybean oil extraction using ethanol and mixtures with p-cymene as co-solvent: Early uses of pore volume and surface diffusion model
Green solvents are widely explored for extracting oil from raw vegetable materials. As an alternative to hexane, ethanol is used in oil extraction but exhibits partial miscibility, requiring a co-solubilizer. p-Cymene, selected based on Hansen solubility parameter (), enhances miscibility due to the reduced distance between solute and solvent, as indicated by the decrease in relative energy difference (). This study evaluated the pore volume and surface diffusion model (PVSDM) for vegetable oil extraction, with statistical results supporting its suitability. The best fits obtained were 0.990, 0.076, and 0.004 for , , and , respectively. The experimental data fit better to the PVSDM than the power-law models. While the So and MacDonald model fit more accurately, inconsistencies arose due to the non-stationary profile of the experimental data. Mechanistically, the PVSDM provided richer insights into mass transfer compared to the mass transfer kinetic model (MTKM). Extraction at 25 °C was influenced by the co-solvent addition, which may aid energy savings. and Fisher tests confirmed the model’s predictive accuracy. These findings are valuable for further exploration of soybean oil as a feedstock for food and biodiesel production.
期刊介绍:
The journal includes papers in the following areas:
– Simple organic liquids and mixtures
– Ionic liquids
– Surfactant solutions (including micelles and vesicles) and liquid interfaces
– Colloidal solutions and nanoparticles
– Thermotropic and lyotropic liquid crystals
– Ferrofluids
– Water, aqueous solutions and other hydrogen-bonded liquids
– Lubricants, polymer solutions and melts
– Molten metals and salts
– Phase transitions and critical phenomena in liquids and confined fluids
– Self assembly in complex liquids.– Biomolecules in solution
The emphasis is on the molecular (or microscopic) understanding of particular liquids or liquid systems, especially concerning structure, dynamics and intermolecular forces. The experimental techniques used may include:
– Conventional spectroscopy (mid-IR and far-IR, Raman, NMR, etc.)
– Non-linear optics and time resolved spectroscopy (psec, fsec, asec, ISRS, etc.)
– Light scattering (Rayleigh, Brillouin, PCS, etc.)
– Dielectric relaxation
– X-ray and neutron scattering and diffraction.
Experimental studies, computer simulations (MD or MC) and analytical theory will be considered for publication; papers just reporting experimental results that do not contribute to the understanding of the fundamentals of molecular and ionic liquids will not be accepted. Only papers of a non-routine nature and advancing the field will be considered for publication.