Characteristics of palm mid-fractions produced from different fractionation paths and their potential usages

Three palm mid-fraction (PMF) groups produced from different fractionation paths were analyzed in terms of the fat, triacylglycerol and sn-2 fatty acid compositions, thermal properties (melting and crystallization behaviors, and solid fat contents (SFCs)), micronutrient levels and oxidative stability indexes (OSIs) to achieve their sufficient utilization. PMF-A (iodine value (IV), 48.4 g/100 g) fractionated from palm olein contained 43.8% 1,3-dipalmitoyl-2-oleoyl-glycerol (POP) and 16.7% 1-palmitoyl-2,3-dioleoyl-glycerol, showing soften properties (slip melting point (SMP), 27.6°C; SFC at 30°C, 2.2%) at hot weather. PMF-B (IV, 42.3 g/100g) obtained from palm stearin showed similar fat and triacylglycerol compositions as PMF-A, but the high 1,2,3-tripalmitoyl-glycerol level (6.2%) improves its thermal behaviors (SMP, 34.9°C; SFC at 30°C, 13.8%). The SFC profiles of PMF-A and PMF-B were comparable to those found in frozen and puff margarine shortenings. Furthermore, both of the PMF groups exhibited excellent OSIs (13.2 and 11.2 h, respectively) because of their high micronutrient levels (especially γ-tocopherol and campesterol). In general, γ-tocopherol and campesterol contribute to preventing lipids from oxidation under frying conditions. Therefore, PMF-A and PMF-B are recommended for manufacturing margarine shortenings and frying fasts. PMF-C (IV, 33.0 g/100g) produced from the additional fractionation of PMF-A or PMF-B contained the highest POP percentage (67.1%) and showed heat-resistant property (SMP, 31.8°C; SFC at 30°C, 22.4%). Its steep SFC profile was superior to that of cocoa butter, suggesting the fat is preferred in producing hard chocolate fats.     

Production of zero trans Iranian vanaspati using chemical transesterification and blending techniques from palm olein, rapeseed and sunflower oils

Chemical transesterification and blending techniques were used for producing zero trans fats suitable for use as Iranian vanaspati. Triple blends of palm olein (POo), rapeseed (RSO) and sunflower oil (SFO) were subjected to two different treatments: (i) blending and then transesterification (BT) and (ii) transesterification of pure POo before blending with RSO and SFO (TB). The changes in slip melting point (SMP), solid fat content (SFC), carbon number (CN) triacylglycerol (TAG) composition, induction period (IP) of oxidation at 120 °C and IP of crystallisation at 20 °C of blends before and after treatments were investigated. Both BT and TB methods resulted in an increase in the CN48 TAG molecules, SMP and SFC, and a decrease in the IP of oxidation and crystallisation of initial blends. Samples made by TB method had higher CN48 TAG content, SMP, SFC and IP of oxidation, and lower IP of crystallisation than those made by BT method. Correlation between SFC at 20 °C and saturated fatty acid (SFA) content of the treated blends indicated that the SFA must be higher than 33.1% and 26.8% for BT and TB methods, respectively, to obtain fats suitable for use as vanaspati.     

Production and characterization of α-linolenic acid enriched structured lipids from lipase-catalyzed interesterification

The purpose of this study was to enrich α-linolenic acid (ALA) on the triacylglycerol (TAG) molecules of the selected vegetable oils (soybean and corn oil) in order to synthesized structural lipid (SL) with low ω6 to ω3 ratio. SLs were synthesized by lipase-catalyzed interesterification of soybean (SO) and corn oil (CO) with perilla oil (PO). Lipozyme RM IM from Rhizomucor miehei (5% by weight of total substrate) was used for the reaction. The reaction was performed during 24 hr at 55°C in the stirred-batch type reactor with solvent free system. After 24 hr reaction the ratio of ω6 to ω3 in SL products dramatically decreased comparing to that of substrates (SO and CO) before the reaction. At sn-2 position, the contents of ALA were 25.99% in soybean-SL and 23.25% in corn-SL, respectively. According to the equivalent carbon number (ECN) of TAG profile, newly produced SLs were separated by reverse-phase high performance liquid chromatography (HPLC). These results indicated that lipase-catalyzed interesterification is effective to produce SL with low ω6 to ω3 ratio which might be used as health beneficial oil.     

Production of trans‐Free Margarine with Stearidonic Acid Soybean and High‐Stearate Soybean Oils‐Based Structured Lipid

Abstract: Omega‐3 fatty acids (n‐3 FAs) have been positively associated with prevention and treatment of chronic diseases. Intake of high amounts of trans fatty acids (TFAs) is correlated with increased risk of coronary heart disease, inflammation, and cancer. Structured lipid (SL) was synthesized using stearidonic acid (SDA) soybean oil and high‐stearate soybean oil catalyzed by Lipozyme^® TLIM lipase. The SL was compared to extracted fat (EF) from a commercial brand for FA profile, sn‐2 positional FAs, triacylglycerol (TAG) profile, polymorphism, thermal behavior, oxidative stability, and solid fat content (SFC). Both SL and EF had similar saturated FA (about 31 mol%) and unsaturated FA (about 68 mol%), but SL had a much lower n‐6/n‐3 ratio (1.1) than EF (5.8). SL had 10.5 mol% SDA. After short‐path distillation, a loss of 53.9% was observed in the total tocopherol content of SL. The tocopherols were lost as free tocopherols. SL and EF had similar melting profile, β’ polymorph, and oxidative stability. Margarine was formulated using SL (SLM) and EF (RCM, reformulated commercial margarine). No sensory difference was observed between the 2 margarines. The SL synthesized in this study contained no TFA and possessed desirable polymorphism, thermal properties, and SFC for formulation of soft margarine. The margarine produced with this SL was trans‐free and SDA‐enriched. Practical Application: The current research increases the food applications of stearidonic acid (SDA) soybean oil. trans‐Free SDA containing SL was synthesized with desirable polymorph, thermal properties, and SFC for formulation of soft margarine. The margarine produced with this SL had no trans fat and had a low n‐6/n‐3 ratio. This may help in reducing trans fat intake in our diet while increasing n‐3 FA intake.     

Feeding hydrogenated palm fatty acids and rumen-protected protein to lactating Holstein-Friesian dairy cows modifies milk fat triacylglycerol composition and structure,and solid fat content

The aim of this study was to analyze the effect of fat and protein supplementation to dairy cattle rations on milk fat triacylglycerol (TAG) composition, fatty acid (FA) positional distribution in the TAG structure, and milk solid fat content (SFC). Fifty-six lactating Holstein-Friesian cows were blocked into 14 groups of 4 cows and randomly assigned 1 of 4 dietary treatments fed for 28 d: (1) low protein, low fat, (2) high protein, low fat, (3) low protein, high fat, and (4) high protein, high fat. The high protein and high fat diets were obtained by isoenergetically supplementing the basal ration (low protein, low fat) with rumen-protected soybean meal and rumen-protected rapeseed meal, and hydrogenated palm FA (mainly C16:0 and C18:0), respectively. Fat supplementation modified milk TAG composition more extensively compared with protein supplementation. Fat supplementation resulted in decreased concentrations of the low molecular weight TAG carbon number (CN) 26 to CN34 and medium molecular weight TAG CN40, CN44, and CN46, and increased concentrations of CN38 and the high molecular weight TAG CN50 and CN52. Increased contents of C16:0, C18:0, and C18:1cis-9 in TAG in response to fat supplementation were related to increases in the relative concentrations of C16:0 and C18:0 at the sn-2 position and C18:0 and C18:1cis-9 at the sn-1(3) positions of the TAG structure. Increased concentrations of high molecular weight TAG species CN50 and CN52 in response to fat supplementation was associated with increased milk SFC at 20, 25, and 30°C. Our study shows that important alterations in milk TAG composition and structure occur when feeding hydrogenated palm FA to lactating dairy cattle, and that these alterations result in an increased SFC of milk fat. These changes in milk SFC and TAG composition and structure may improve absorption of both fat and minerals in milk-based products for infants and may affect processing of milk fat.     

Lipase-catalyzed acidolysis of palm olein and caprylic acid in a continuous bench-scale packed bed bioreactor

Enzymatic acidolysis of refined, bleached and deodorized (RBD) palm olein with caprylic acid was carried out in a continuous packed bed bioreactor to produce structured lipid (SL) that can confer metabolic benefits when consumed. Lipozyme^® IM 60 from Rhizomucor miehei, a 1,3-specific lipase, was used as the biocatalyst in this study. After 24 h of reaction, 30.5% of the total fatty acid content of the modified oil was found to be caprylic acid, indicating its incorporation into the palm olein. The triacylglycerols (TAGs) of palm olein after acidolysis were separated and were characterized by seven clusters of TAG species with equivalent carbon number (ECN), C28, C30, C32, C34, C36, C38 and C40. Caprylic–oleic–caprylic TAGs were predicted in cluster C32, which recorded the highest amount, with 35.3% of the total TAG. Fatty acid composition at the sn-2 position was determined, by pancreatic lipolysis, as C8:0, 9.2%; C12:0, 2.3%; C14:0, 1.8%; C16:0, 21.3%; C18:0, 4.7%; C18:1, 60.7%. Iodine value (IV), slip melting point (SMP) and differential scanning calorimetric (DSC) analyses of SL were also performed. In IV analysis, SL recorded a drop of value from 60.4 to 48.2 while SMP was reduced from 13 to 4.2 °C, in comparison to RBD palm olein. DSC analysis of SL gave a melting profile with two low melting peaks of −15.97 and −11.78 °C and onset temperatures of −18.43 and −14.03 °C, respectively.     

Rheological characteristics of vegetable oils as affected by deep frying of French fries

Fatty acid composition and rheological characteristics of sunflower oil (SO), cottonseed oil (CO) and palm olein (PO) during deep frying for 4–16 h were investigated. In the different oils, linoleic acid decreased while palmitic, stearic and oleic acids increased in the bath oil during frying. Total phenolic content (TPC) in different oils increased during frying and strongly correlated with frying time. As frying progressed, it was observed that the rate of increase in TPC was relatively slower in PO than in the SO and CO. The shear stress versus shear rate results was fitted to Newtonian, Bingham and Herschel–Bulkley rheological models. The flow behaviour of fresh and fried SO, CO and PO was recorded at 25 °C. Fresh oils showed Newtonian behaviour with correlation coefficients greater than 0.99 at 25 °C and slight non-Newtonian behaviour after frying. Palm olein showed higher increase in viscosity in comparison to CO and SO. Rheological parameters of vegetables oils showed great changes, wherein the highest change in viscosity was recorded after 16 h of frying. Palm olein had higher flow behavior parameters than SO and CO. The increase in frying time caused an increase in K, η_B, τ_0HB, τ_0B, and η values, while the n values decreased with increasing the frying time. The viscosities of oils were plotted against the levels of C18:1 and C18:2 wherein highly positive correlations were found between them (R² = 0.99). The temperature dependence of viscosity was studied by using the Arrhenius relationship and the activation energy indicates the sensitivity of viscosity to changes in temperature. It could be concluded that the rheological parameters can provide an overall estimate of oil quality during frying.     

Influence of lipid composition, crystallization behavior and microstructure on hardness of palm oil-based margarines

Two typical commercial palm oil-based margarines, denoted A (complained as with over-hardness) and B (commercially considered as with acceptable hardness), respectively, were compared in terms of hardness, solid fat content (SFC), lipid composition [fatty acid and triacylglycerol (TAG) composition], crystallization behavior and microstructure. On the basis of these results, the reason of over-hardness in margarine A was discussed. Margarine A showed higher hardness than margarine B with the differences increasing along with rise in temperature in the typical range from 15 to 30 °C. While margarine B has good quality and appropriate hardness, it showed SFCs higher than margarine A. Lipid composition analyses showed that margarine B has small amounts of medium chain fatty acids and higher content of monounsaturated TAGs [1,3-dipalmitoyl-2-oleoyl-glycerol (POP), 1,3-dipalmitoyl-2-linoleoyl-glycerol (PLP), 1-palmitoyl-2-oleoyl-3-stearoyl-glycerol (POS)]. X-ray diffraction analysis revealed that both margarines have β′ and β polymorphs with the β form being dominant in margarine B. Isothermal crystallization kinetics of both margarines under 15, 20, 25, and 30 °C, respectively, fitted using the Avrami model indicates that margarine B hardly crystallizes at temperatures ≥25 °C. Morphologic observations of the microstructure of both margarines by polarized light microscope and scanning electron microscopy showed that formation of large spherulites have an important influence on margarine texture. Occurrence of large spherulites in margarine B is considered to decrease the numbers of crystals and lessen mutual attraction with temperature increasing, which leads to weakened strength of the total network, even if margarine B has a higher SFC value.     

Physicochemical Properties and Sensory Attributes of Medium- and Long-Chain Triacylglycerols (MLCT)-Enriched Bakery Shortening

Six binary formulations of medium- and long-chain triacylglycerols (MLCT) fat and palm stearin and four ternary formulations of MLCT fat, palm stearin, and palm olein were produced. MLCT fat and palm stearin were mixed in ranges of 40–90% with 10% increments (w/w), while for the ternary formulations, 10% and 20% palm olein were substituted to palm stearin in MS 46 and MS 55 formulations. The solid fat content (SFC) by pulsed nuclear magnetic resonance and heating profiles using differential scanning calorimeter of these formulations were determined. Results obtained from SFC and heating profiles found that all the formulations melted completely at 55 °C. The high complete melting temperature is due to the stearic acid content in MLCT fat. Generally, increasing % MLCT fat (40–90%) in the formulations lowers the SFC curves at the measured temperatures (0–60 °C). The binary samples of MS 73, MS 82, and MS 91 showed SFC between 15% and 25% at room temperature (25 °C), which indicated that these formulations were suitable for shortening production. As the production cost of MLCT fat is high (approximately USD 3/kg), an attempt to reduce the proportion of MLCT fat in the shortening formulations was done by developing the ternary formulations. Shortenings formulated with 40:40:20 (MSO 442), 50:40:10 (MSO 541), and 50:30:20 (MSO 532) of MLCT fat/palm stearin/palm olein formulations had similar SFC% at 25 °C, and they were subsequently chosen to produce shortening. Using multivariate analysis, taste attribute showed positively and highly correlated to the melting temperature and SFC at 25 °C of the MLCT-enriched shortenings. In acceptance test, high correlation (R ² = 0.98) was only found on cakes made from MSO 442 and MSO 541 shortenings. Both untrained and trained panelists rated the Madeira cakes made from MSO 532 shortening the highest for overall acceptability.     

Modifying the physical properties of butter using high-intensity ultrasound

The physical qualities of butter are affected by the physical properties of the cream used to make it. The objective of this study was to evaluate the effect of high-intensity ultrasound (HIU) on the physical properties of cream and butter. High-intensity ultrasound (frequency: 20 kHz, amplitude: 108 µm), often called sonication, was applied for 0, 10, 30, 60, and 90 s using a 1.27-cm-diameter tip to heavy cream (40% fat; 300 g) that was aged at 7.5°C with low agitation (40 rpm) for 90 min. Sonicated cream was churned at 7.5°C until butter grains were formed. The solid fat content (SFC), melting behavior, and average fat droplet size of cream were measured after HIU treatment. Butter was characterized by SFC and melting behavior immediately after production and was tested for SFC, melting behavior, and hardness after storage for 24 h at 5°C. High-intensity ultrasound did not affect the average fat droplet size of cream. Sonicating cream for 30, 60, and 90 s slightly decreased SFC due to the temperature increase (2–6°C) that occurred during HIU application. Two melting peaks were observed at approximately 17 and 33°C in all the cream samples. A significantly lower peak temperature was observed in cream sonicated for 10 s compared with creams sonicated for 30 and 60 s. A relatively shorter churning time of sonicated cream compared with nonsonicated cream was observed, possibly because HIU weakens the fat globule membrane. Two melting peaks were observed in all butter samples at approximately 16 and 33°C. Treatment with HIU for 10 to 60 s significantly increased the hardness of butter. When HIU was applied to cream for 10 s, the hardest butter was obtained, with the lowest onset temperatures and highest enthalpy values for both melting peaks. Treatment with HIU for 10 s promoted crystallization of low-melting-point triacylglycerols (TAG) during churning, which resulted in a harder material. Significantly lower enthalpy values for the high-melting-fraction TAG were observed in butters treated with HIU for 60 and 90 s compared with non-HIU-treated butter, which suggests that a longer duration of HIU promotes melting of high-melting-point TAG. The hardness of butter was correlated with the enthalpy values of the low-melting fraction and with total enthalpy values of fresh butter. However, further crystallization occurred in the butter during 24 h of storage at 5°C, and all differences in enthalpy values disappeared. In conclusion, exposure of cream to HIU can be used to modify the physical properties of butter, and the effects of HIU depend on the length of HIU treatment.     

Increasing the oxidative stability of soybean oil through fortification with antioxidants

Vegetable oils high in polyunsaturated fatty acids (PUFA), like soybean oil (SO), are known for lowering the risk of consumers for contracting cardiovascular disease as well as improving cognitive health. However, they are more susceptible to lipid oxidation than recently introduced high‐oleic cultivars like high‐oleic sunflower oil (HOSFO). Thus, the objective of this study was to increase the stability of PUFA oils to maintain the aforementioned health benefits by supplementing them with industrially relevant antioxidant compounds that prevent or delay oxidation during food production and storage. Herein, a variety of synthetic and natural antioxidants tested alone or in mixtures was screened to bring the stability of SO closer to that of HOSFO. Oils were stored under accelerated conditions (35 °C) in the dark for 28 weeks, and the evolution of primary (hydroperoxides) and secondary (hexanal) lipid oxidation products was monitored. Oxidative stability index data showed that addition of 300 ppm of ascorbyl palmitate (AP) stabilised SO to the greatest magnitude. Further, a combination of AP (300 ppm) and M‐TOC (1000 ppm) was able to limit hydroperoxide and hexanal formation in SO at 35 °C for 12 weeks. It was demonstrated that assessing multiple quality parameters for lipid stability are a necessary undertaking.     

Synthesis of confectionery fat from illipé butter stearin and palm mid-fraction blend via enzymatic interesterification

Cocoa butter equivalent (CBE) was synthesised from blends of illipé butter stearin (IBS) and palm mid-fraction (PMF) via enzymatic interesterification (EIE). IBS was blended with PMF in three wt ratios (70:30, 60:40 and 50:50) and the EIE reactions were performed at 50°C for 30 min using an sn-1,3-specific lipase from Rhizopus oryzae as a catalyst. The triacylglycerol (TAG) compositions, slip melting points (SMP), crystallisation and melting thermograms, solid fat content (SFC) curves, and crystal microstructure of the blends before and after EIE were studied and compared with cocoa butter (CB). After EIE, the contents of POP and StOSt decreased, whereas the POSt content increased in all blends. Blend EIE 60:40 exhibited the POP and StOSt contents that situated within the ranges of POP and StOSt contents of CB. It also showed SMP, melting peak and melting completion temperatures, melting enthalpy and crystal microstructure most similar to CB. Most importantly, its SFC curve completely matched that of CB. Consequently, EIE 60:40 was chosen for further investigation and it was found to be fully compatible with CB and crystallised into the same polymorphic form (β) as CB. Therefore, EIE 60:40 has a high potential for use as a commercial CBE.     

Enzymatic synthesis of medium‐ and long‐chain triacylglycerols–enriched structured lipid from Cinnamomum camphora seed oil and camellia oil by Lipozyme RM IM

Medium‐ and long‐chain triacylglycerols (MLCTs)–enriched structured lipid (SL) was synthesised through enzymatic interesterification from Cinnamomum camphora seed oil (CCSO) and camellia oil (CO) using Lipozyme RM IM from Rhizomucor miehei as a biocatalyst. Effects of different reaction conditions including substrate molar ratio, reaction time and reaction temperature were investigated. Results showed that 55.81% of total MLCT species (CCO/LaCL, LaCO/LCL, COO/OCO and LaOO/OLaO) was obtained in the interesterified product under the optimal conditions of substrate molar ratio of 1:1.5 (CCSO/CO) at 60 °C for 3 h. Thereafter, fatty acid profiles, tocopherol contents and physiochemical characteristics of the interesterified product and physical blend were comparatively investigated. The fatty acid composition of the interesterified product consisted of capric acid (26.33%), lauric acid (21.29%) and oleic acid (42.33%). It should be mentioned that the interesterified product contained predominantly oleic acid (88.69%) at Sn‐2 position, while MCFAs (68.05%) at Sn‐1,3 positions. Compared with physical blend, the reduction in tocopherol contents and changes of physiochemical characteristics occurred in SL. The smoke point of the interesterified product was much higher than that of the physical blend, which meant that such MLCTs‐enriched SL could be better for cooking purpose.     

The Effects of Subcritical Water Treatment on Antioxidant Activity of Golden Oyster Mushroom

Subcritical water (SCW) extraction of golden oyster mushroom (GOM) was carried out at various temperatures (50, 100, 150, 200, 250, and 300 °C) for 10, 30, and 60 min, and the antioxidant and certain physiological activities of the extracts were evaluated. SCW treatment of GOM increased the antioxidant activity of the extracts. The SCW extraction of GOM at 250 °C for 60 min or 300 °C for 30 min showed relatively high levels of total phenolic content, 1,1-diphenyl-2-picrylhydrazyl radical scavenging activity, and reducing power. The β-glucan content was the highest when SCW extraction was carried at 200 °C for 60 min, while the highest 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) radical scavenging activity occurred at 300 °C for 60 min. These results indicate that the temperature and time of SCW extraction significantly affect the antioxidant activity as well as the nutraceutical compound levels of GOM extracts.     

Improvement of palm oil and sunflower oil blends by enzymatic interestrification

Palm oil (PO) and sunflower oil (SFO) blends with varying proportions were subjected to enzymatic interesterification (EIE) using a 1,3‐specific immobilised lipase. The interesterified blends were evaluated for their slip melting point (SMP), solid fat content (SFC) at 10–40 °C, p‐anisidine value, peroxide value, free fatty acids (FFA), induction period of oxidation at 110 °C (IP110) and composition of fatty acids by gas chromatography. Under EIE treatment, the blends of PO and SFO in different proportions (20:80, 40:60, 50:50, 60:40 and 80:20) had saturated and unsaturated fatty acid content in the range of 37.6–52.0% and 48.0–62.4%, respectively. The blends showed a considerable reduction in their SFC, SMP, peroxide value and oxidative stability at 110 °C, but presented increase in FFA and p‐anisidine value. The optimum condition for minimising the fatty acid in oil was obtained, at 64 °C, using 8.9% enzyme and 3 h reaction time.     

Effects of Roasting Conditions on the Changes of Stable Carbon Isotope Ratios (δ13C) in Sesame Oil and Usefulness of δ13C to Differentiate Blended Sesame Oil from Corn Oil

Abstract: Differentiating blended sesame oils from authentic sesame oil (SO) is a critical step in protecting consumer rights. Stable carbon isotope ratios (δ¹³C), color, fluorescence intensity, and fatty acid profiles were analyzed in SO prepared from sesame seeds with different roasting conditions and in corn oil blended with SO. Sesame seeds were roasted at 175, 200, 225, or 250 °C for 15 or 30 min at each temperature. SO was mixed with corn oil at varying ratios. Roasting conditions ranging from175 to 250 °C at the 30 min time point did not result in significant changes in δ¹³C (P > 0.05). Values of δ¹³C in corn oil and SO from sesame seeds roasted at 250 °C for 15 min were −17.55 and −32.13 ‰, respectively. Fatty acid ratios, including (O + L)/(P × Ln) and (L × L)/O, where O, L, P, and Ln were oleic, linoleic, palmitic, and linolenic acids, respectively, showed good discriminating abilities among the SO blended with corn oil. Therefore, using different combinations of stable carbon isotope ratios and some fatty acid ratios can allow successful differentiation of authentic SO from SO blended with corn oil. Practical Application: Adulteration of sesame oil with less expensive oils such as corn oil or soybean oil to reduce cost is a common unethical practice in Korea. Due to the unique and strong flavor of sesame oils that may mask other weaker flavors, however, differentiating authentic sesame oils from blended oils is difficult. This study showed that the roasting process did not significantly affect the ratios of the stable carbon isotope (δ¹³C) in sesame oils. δ¹³C was confirmed to be a reliable parameter. Moreover, some fatty acid ratios were designed to discriminate between blended sesame oil with corn oil and authentic sesame oil.     

Effect of Temperature on the Crystalline Form and Fat Crystal Network of Two Model Palm Oil-Based Shortenings During Storage

Fat products experienced undesirable microstructural property changes due to the temperatures during transportation and storage. In this study, the lipid composition and solid fat content (SFC) of two model palm oil-based shortenings, which are denoted as shortening A (melting point of 35.1°C) and shortening B (melting point of 51.2°C), were evaluated, and their crystallization behavior and polymorphism during storage at various temperatures (?10 °C to 30 °C) was examined by X-ray diffraction (XRD) and polarized light microscopy (PLM). The fractal dimension (D _b) was calculated to qualify the change in the crystal network during storage. The aggregation of high-melting triacylglycerols (TAGs) nanostructure and the formation of the most stable β polymorph were observed in shortening at higher temperatures (≥0 °C) during storage. At the same temperature, the intensity of β crystals in the two samples increased as the storage time increased, and this trend was obvious at high temperatures (≥10 °C). In addition, the intensity of the β crystals in the two samples gradually increased as the temperature increased, and the size of the crystalline particles became larger. The crystal size in shortening A was larger than that in shortening B at high temperatures (≥10 °C). The crystal network of shortening B was denser than that of shortening A. The D _b value reached a maximum at 10 °C and 30 °C for shortening A and B, respectively. These findings have important implications on the storage stability and functional properties of palm oil-based shortenings.