TY - JOUR
T1 - Comparing electrostatic separation of soy and lupin
T2 - Effect of de-oiling by solvent extraction
AU - Politiek, Regina G.A.
AU - Dijkink, Bert H.
AU - van den Boogaard, Leïla M.
AU - Keppler, Julia K.
AU - Schutyser, Maarten A.I.
AU - Bruins, Marieke E.
PY - 2023/9/15
Y1 - 2023/9/15
N2 - Electrostatic separation is a sustainable dry separation technique based on triboelectric charging of different cellular tissue components (i.e. protein bodies and fibres). This research aimed to determine the mechanism behind the ineffective electrostatic separation of soy and if it could be altered by de-oiling. Several scenarios were compared, which involved electrostatic separation of soy and lupin de-oiled with different solvents (none, acetone, ethanol and hexane). Separation of lupin resulted in a higher true protein content (58.5%DM (dry matter) (Nfactor = 5.7)) than separation of soy (45.0%DM protein). Separation was less effective for soy because its protein bodies were still embedded in the cellular structure after impact milling, which was also reflected in the larger particle size and lower small particle dispersibility. De-oiling soy with hexane and extra milling improved the purity of soy protein-enriched fractions (59.6%DM protein) reaching more similar purity as for lupin protein-enriched fractions. The protein purity of lupin fractions could be increased most via the use of polar solvents (acetone and ethanol). Better electrostatic separation after de-oiling and extra milling for soy could be explained by increased liberated protein bodies, which was key towards the improved separation of soy obtaining protein purities closer to that of pure protein bodies.
AB - Electrostatic separation is a sustainable dry separation technique based on triboelectric charging of different cellular tissue components (i.e. protein bodies and fibres). This research aimed to determine the mechanism behind the ineffective electrostatic separation of soy and if it could be altered by de-oiling. Several scenarios were compared, which involved electrostatic separation of soy and lupin de-oiled with different solvents (none, acetone, ethanol and hexane). Separation of lupin resulted in a higher true protein content (58.5%DM (dry matter) (Nfactor = 5.7)) than separation of soy (45.0%DM protein). Separation was less effective for soy because its protein bodies were still embedded in the cellular structure after impact milling, which was also reflected in the larger particle size and lower small particle dispersibility. De-oiling soy with hexane and extra milling improved the purity of soy protein-enriched fractions (59.6%DM protein) reaching more similar purity as for lupin protein-enriched fractions. The protein purity of lupin fractions could be increased most via the use of polar solvents (acetone and ethanol). Better electrostatic separation after de-oiling and extra milling for soy could be explained by increased liberated protein bodies, which was key towards the improved separation of soy obtaining protein purities closer to that of pure protein bodies.
KW - Defatting
KW - Dry fractionation
KW - Green solvent
KW - Protein enrichment
KW - Triboelectric separation
U2 - 10.1016/j.lwt.2023.115290
DO - 10.1016/j.lwt.2023.115290
M3 - Article
AN - SCOPUS:85171371916
SN - 0023-6438
VL - 187
JO - LWT
JF - LWT
M1 - 115290
ER -