Table 1. Brief information about some studies discussing mitigation of 3-monochloropropane-1,2-diol (3-MCPD) and glycidyl ester (GE) during refining steps.
Oil type | Operation/step | Condition | Effect | Reference |
---|---|---|---|---|
Crude palm oil | Prewashing (applied prior to degumming) | 20 min at 70 °C, 10 % deionised water | At the end of the physical refining, 2- and 3-MCPDE (w=0.54 and 1.04 mg/kg, respectively) were 19 and 22 % lower when prewashing was applied | (108) |
Crude palm oil | Neutralisation | 20 min at 70 °C with 2 L of 33 % NaOH solution | w(3-MCPDE) was reduced by 43 % but w(GE) was doubled | (108) |
Crude palm oil | Neutralisation (only the addition of alkali, refining step was not like industrial practice) | 1 mmol/kg NaHCO3 | w(3-MCPDE) and w(GE) reduced 81 and 84 %, respectively | (5) |
Crude palm oil | Neutralisation | KOH and NaOH were used (other conditions not given) | w(3-MCPDE) reduced 35 % and 45 % when NaOH and KOH were used, respectively | (20) |
Pre-refined palm oil | Bleaching | w(Tonsil Optimum 214 FF bleaching earth)=0.8 % was added to the oil (90 °C, up to 1 kPa) and removed by filtering after 20 min treatment | w(3-MCPDE and related ester) was reduced from 6.06 to 2.48 mg/kg (59 % reduction) | (89) |
Peanut oil (pressed) | Bleaching | The degummed oil was preheated to 95 °C and bleached by adding activated clay (activated by 3 % hydrochloric acid) up to 1 kPa and then filtered after 25 min treatment | w(3-MCPDE) was reduced by approx. 15–22 % after bleaching. Although DGF standard method C-VI 18 (10) of the German Society for Fat Science was used, GE results were not given | (37) |
Crude soybean oil | Degumming, neutralisation, bleaching and deodorisation | Use of acid in the degumming stage and acid-activated clay | w(3-MCPDE) increased compared to crude oil | (109) |
Crude palm oil | Degumming | Acid degumming (0.06 % of 85 % H3PO4 for 20 min at 90 °C) and water degumming (1 % water, 10 min at 90 °C) | Reduction ranging from 56 to 78 % for w(3-MCPDE) and 49–56 % for w(GE) | (110) |
Rice bran oil and palm oil | Bleaching | 20 g oil was bleached with 200 mg activated earth at 110 °C and 10 kPa, after 20 min, cooled to 30 °C and filtered | w(GE) of the model oil spiked with different ester forms of glycidol was reduced effectively to ˃0.1 mg/kg | (72) |
Crude palm oil | Bleaching | At 105 °C for 20 min with acid-activated bleaching earth (1, 2 and 3 %) | w(3-MCPDE) reduced as bleaching earth content increased | (38) |
Crude palm oil | Bleaching | At 95 °C for 20 min with w(clay)=0.5 % | The use of low Cl bleaching earth resulted in lower w(MCPD) than the use of high Cl bleaching earth | (111) |
Crude palm oil | Bleaching | w(pure-Flo B80 natural bleaching earth)=10 % | Bleaching reduced 93 % of w(GE) formed during deodorisation, while w(3-MCPDE) were unaffected | (29) |
Palm oil | Deodorisation | 10 g sample was heated to 200–290 °C for 45–360 min; 20 kg/t steam was purged | Despite the increase in deodorisation temperature to 270 °C, the 3-MCPDE+GE content in the samples increased. Deodorisation for 240-360 min at 290 °C resulted in a decrease in contaminant levels | (20) |
Peanut oil (pressed) | Deodorisation | At 220-260 °C up to 3 h under 200 Pa with steam speed of 0.1 g/min | w(3-MCPDE and related matter) were reduced after 2 h of deodorisation | (37) |
Crude palm oil | Bleaching | w(zeolite-Fe)=1.5–15 % and different bleaching temperature (60–140 °C) | The most effective bleaching procedure was achieved with a w(zeolite-Fe)=5 % and a bleaching temperature of 80 °C for 30 min | (112) |
Palm oil | Bleaching | Using activated carbon treated with a 2 M HCl solution | w(3-MCPD) 80 % reduction and w(GE) 97 % reduction | (113) |
Palm oil | Bleaching | Using metal-organic frameworks (MOFs) | The MOFs, which are composed of 2,6-naphthalenedicarboxylic acid (Fe-MIL-88_BDC), exhibited the most effective adsorption capabilities | (114) |
Palm oil | Bleaching | Using zeolite | The use of beta zeolites led to the most effective removal of 3-MCPDE (86 %) compared to other zeolites tested. Using a synergistic blend of beta zeolite and AC, the efficiency of removing 3-MCPDE was significantly improved to 94 %, resulting in a simultaneous reduction of 75 % in GE | (115) |
Coconut oil | Bleaching | At 105 °C with w(activated clay)=1 %. Bleaching was performed under vacuum. After 30 min, the slurry was allowed to cool (to 50 °C) and filtered | In crude coconut oil w(3-MCPDE) and w(GE) were 0.21 and 0.29 mg/kg, respectively. After bleaching, w(3-MCPDE) remained the same, but w(GE) was reduced to 0.19 mg/kg | (116) |
Camellia oil | Degumming, bleaching and deodorisation | Degumming water addition at 2.97 %, bleaching earth (acid activated) 2.69 %, deodorisation temperature 230 °C, deodorisation duration 90 min | w(3-MCPDE) reduced by 76.9 % | (116) |
Palm olein oil | Bleaching and deodorisation | Bleaching; 95 °C up to 1 h under 8 kPa using neutral and acid-activated bleaching earth Deodorisation (at 200–230 °C up to 1.5 h under 0.15–0.2 kPa) |
Use of neutral bleaching earth and deodorisation at 230 °C led to w(MCPD) reduction of 69.91 %. The glycidol esters may be effectively reduced by up to 93.85 % with the use of acid-activated bleaching earth and deodorisation at a temperature of 230 °C, without the need for neutralisation | (117) |
Palm oil | Deodorisation | At 250 °C up to 2 h using 100 g bleached oil | Potassium acetate reduced w(3-MCPDE) almost 99 % and w(GE) 40 %. Sodium hydrogencarbonate, sodium acetate and sodium carbonate were able to lower w(3-MCPDE) by more than 80 % | (118) |
Palm oil | Deodorisation | Different temperatures (210–270 °C) and time (30–120 min) | After 30 min at 210 °C, the formation of 3-MCPDE was most pronounced under the mildest conditions | (119) |
High oleic sunflower and rapeseed oil | Water washing, degumming, bleaching and deodorisation | Different deodorisation temperatures (220–260 °C), at 70 °C up to 20 min using 0.5 % citric acid for degumming, at 95 °C up to 20 min with 3 different bleaching earth (0.1–2 %) | Double refining successfully decreased w(GE) in high oleic (HO) sunflower and rapeseed oil by 70 and 94 %, respectively | (120) |