Kinetic study of the microwave-induced thermal degradation of cv. Arbequina olive oils flavored with lemon verbena essential oil

The effect of typical domestic microwave heating (0–15 min, at 800 W) on the thermal degradation of unflavored and flavored olive oils' minor bioactive compounds and related antioxidant activity was studied. Olive oils from cv. Arbequina were flavored with lemon verbena essential oil (0%, 0.2% and 0.4%, w/w) leading to a linear increase of total phenols (112–160 mg gallic acid kg⁻¹ oil, R-Pearson = +0.9870), total carotenoids (2.19–2.56 mg lutein kg⁻¹ oil, R-Pearson = +0.9611), and, to a less extent, of chlorophyll (2.32–3.19 mg pheophytin kg⁻¹ oil, R-Pearson = +0.8238). However, no such linear trend was observed for the oxidative stability (6.5–7.8 h) or the radical scavenging activity (inhibition rates: 40%–43%). The contents of total phenols, total carotenoids, and chlorophyll decreased with the rise of the microwave heating time, following their thermal degradation, a second-order kinetic model (0.8784 ≤ R-Pearson ≤ 0.9926). The essential oil addition did not influence the estimated second-order rate reaction constants of total phenols (0.00070–0.00072 kg oil min⁻¹ mg⁻¹ gallic acid)and total carotenoids (0.14–0.17 kg oil min⁻¹ mg⁻¹ lutein), with a broader variation observed for chlorophyll (0.014–0.022 kg oil min⁻¹ mg⁻¹ pheophytin). Globally, total carotenoids degraded faster than total phenols and chlorophyll (half-life of 2.3–3.4, 8.8–12.8, and 14.5–30.8 min, respectively). Moreover, except for chlorophyll, the half-life of total phenols and carotenoids linearly decreased with the essential oil addition (R-Pearson: −0.9999 and −0.9421, respectively), showing that flavoring did not have a protective effect against degradation when subjected to a microwave heating.     

Impact of high-intensity ultrasound on physical properties and degree of oxidation of lipase modified menhaden oil with caprylic acid and/or stearic acid

The purpose of this research was to determine the effect of high-intensity ultrasound (HIU) on physical properties, degree of oxidation, and oxidative stability of structured lipids (SLs). Caprylic acid (C) and stearic acid (S) were incorporated into menhaden oil using Lipozyme® 435 lipase to obtain five samples: (1) LC 20 (menhaden oil with 20% of C), (2) LC 30 (menhaden oil with 30% C), (3) LS 20 (menhaden oil with 20% S), (4) LS 30 (menhaden oil with 30% S), and (5) Blend C (menhaden oil with 16.24% C and 13.04% S). Samples were crystallized for 90 min at the following temperatures: (1) LC 20 at 15.5°C, (2) LC 30 at 17.5°C, (3) LS 20 at 24°C, (4) LS 30 at 30°C, and (5) Blend C at 18.0°C, and HIU was applied at the onset of crystallization. Physical properties, degree of oxidation, and oxidative stability were evaluated in sonicated and nonsonicated samples. All SLs had statistically higher G′ after sonication. Sonicated LS 30, LC 30, and Blend C had a higher melting enthalpy than the nonsonicated ones, while enthalpy values in sonicated LS 20 and LC 20 samples were not statistically different than the nonsonicated ones. No significant difference between sonicated and nonsonicated samples was observed in peroxide values (1.2 ± 0.1 meq/kg, p > 0.05) and in the oxidative stability index (6.3 ± 0.2 h, p > 0.05). These results showed that HIU was effective at changing physical properties without affecting the oxidation of the samples.     

A new spectrophotometric method for the rapid assessment of deep frying oil quality

A new and quick spectrophotometric method was developed to assess deep-frying oil quality. The scanned spectrophotometric curves of the frying oil samples from 350 and 650 nm wavelength changed systematically with the duration of deep frying. The absorbances of the frying oil samples, especially those measured at 490 nm, increased significantly during frying and were significantly correlated to frying time (r ≥0.95, P<0.001). There was a strong correlation between the absorbances of a set of oil samples taken from 0 to 80 h of deep frying and total polar compound contents in the same set of oil samples analyzed using the American Oil Chemists' Society official method (r=0.974, P<0.001). The equation for conversion of the absorbances to total polar compound contents is y=−2.7865x ² +23.782x+1.0309. The absorbances of 10 different types of frying oils with samples taken from 0 to 80 h of deep frying in duplicate were also strongly correlated to total polar compounds in the same oil samples (r=0.953, P<0.001, n=220). The results show that this method is fast, simple, convenient, and reliable.     

Liquid to Semisolid Rheological Transitions of Normal and High-oleic Peanut Oils upon Cooling to Refrigeration Temperatures

Rheological transitions of peanut oils cooled from 20 to 3 °C at 0.5 °C/min were monitored via small strain oscillatory measurements at 0.1 Hz and 1 Pa. Oils were from nine different cultivars of peanut, and three oils were classified as high-oleic (approximately 80% oleic acid). High-oleic oils maintained an overall liquid-like character at 3 °C for 2 h. In contrast, several normal (non high-oleic) peanut oils displayed a predominantly elastic (solid-like) response after 2 h at 3 °C. Increases in viscoelasticity were associated with lipid crystallization events as confirmed by DSC. The higher (p < 0.001) liquid viscosities and increased (p < 0.001) contents of oleic acid, which has a more non-linear structure as compared to other fatty acids typical in these oils, were hypothesized to hinder crystallization in high-oleic oils. Changes in viscoelasticity at 3 °C were greatest for three normal oils that had the significantly (p < 0.001) highest content of C20:0 and/or C22:0 fatty acids, and these long, saturated hydrocarbon chains are hypothesized to promote crystallization. No peanut oil maintained clarity after 5.5 h at 0 °C (modified cold test used to screen salad oils); however, these data as a whole suggest strategies for breeding and/or processing peanut oils for enhanced resistance to crystallization. The use of trade names in this publication does not imply endorsement by the United States Department of Agriculture: Agricultural Research Service.     

Effect of omega fatty acid-rich oil blend supplementation on the growth,carcass, meat quality,and gene expression of Barbari goats

This study investigated the effect of supplementing omega fatty acids-rich oil blend, composed of sunflower oil (1.5% and 3.0%), linseed oil (1.5% and 3.0%), and FineXNV1810 (20 g) on the carcass, meat quality, fatty acid profile, and genes (peroxisome proliferator-activated receptor-α, stearoyl-CoA desaturase, acetyl-CoA carboxylase, hydroxy-3-methylglutaryl coenzyme A, and leptin) of Barbari goats. The goat kids (n = 18) were divided into three groups, namely, group A: basal diet; group B: basal diet + oil blend level 1; and group C: basal diet + oil blend level 2, and subjected to the feeding trial for 120 days followed by slaughter and meat quality studies. No treatment effect was recorded in carcass characteristics, pH, water holding capacity, and proximate composition of meat. However, a significant (p < 0.05) treatment effect was observed in cooking loss, lightness, yellowness, and shear force values of meat. There were significant differences (p < 0.05) in linoleic acid, α-linolenic acids, conjugated linoleic acid (CLA), polyunsaturated fatty acids (PUFA), n − 3 and n − 6 PUFA, PUFA/saturated fatty acids and n − 6/n − 3 ratios, and thrombogenic index among groups. An upregulation of the studied genes in the supplemented groups was observed. There were upregulations in the studied genes in the supplemented groups. Practical applications: Goat meat is in great demand the world over, especially in tropical countries, including India, and does not carry any social or religious prohibition. Although goat meat has relatively less fat, consumers express their concern over the presence of undesirable fatty acids. The present study shows that the fatty acid configuration of goat meat can be improved by a dietary supplementation of an oil blend rich in omega fatty acids. The amount of n − 3 PUFA, n − 6 PUFA, and CLA in goat meat was significantly increased due to the dietary oil blend making it healthy for the consumers. Moreover, the dietary oil blend at the studied levels did not significantly affect the growth and meat quality parameters of the goats. Thus, the studied approach can be successfully followed to produce healthier goat meat.     

Sonocrystallization of a Palm-Based Fat with Low Level of Saturation in a Scraped Surface Heat Exchanger

Physical properties of fats are affected by the reduction of saturated fatty acids. One method for retaining desired properties is the use of high-intensity ultrasound (HIU). The aim of this study was to investigate the influence of HIU power levels, pulse time, and position on the physical properties of a low-saturated palm-based fat crystallized in a scraped surface heat exchanger (SSHE). The sample was crystallized in a SSHE at 26 °C, using a 11 L hour⁻¹ flow rate, and agitation of 344 rpm in the barrels and 208 rpm in the pin worker. HIU was applied using a 12.7 mm tip coupled to a water jacketed (26 °C) flow cell that was placed at the end of the SSHE process. Sonication conditions were 20%, 50%, or 80% amplitude using pulses (5 and 10 s) or continuous sonication. After choosing the best HIU condition, the position of the flow cell was changed to different positions within the SSHE: before the first barrel (HIU-0), between the two barrels (HIU-1), between the second barrel and the pin worker (HIU-2), and after the pin worker (HIU-3). The best sonication condition from the first set of experiments was when HIU was applied using 50% amplitude and 10 s pulses. This condition resulted in higher oil binding capacity (OBC) and storage modulus (G') compared to the non-sonicated sample (OBC: 77% against 69.5%; G':154 kPa against 108 kPa). The best HIU position was HIU-3 since no further agitation was applied. The lack of agitation after sonication induced secondary nucleation and generated a strong crystalline network.     

Effect of Lactose Monolaurate and High Intensity Ultrasound on Crystallization Behavior of Anhydrous Milk Fat

Crystallization behavior of anhydrous milk fat (AMF) was studied with the addition of 0.025 and 0.05 % lactose monolaurate (LML). The crystallization behavior was studied at low (ΔT = 3 °C) and high supercooling (ΔT = 6 °C). Polarized light microscopy and laser turbidimetry indicated a delay in crystallization on addition of 0.025 % and 0.05 % LML or Tween 20 to AMF. High intensity ultrasound (HIU) was applied to AMF samples with 0.05 % LML and lower supercooling (T _c = 31 °C; ΔT = 3 °C). HIU application in AMF and AMF + 0.05 % LML induced crystallization (p < 0.05) changing the induction time (τ) at 31 °C from 34.20 ± 1.67 min (AMF) and 47.07 ± 1.27 min (AMF + 0.05 % LML) to 23.23 ± 3.26 min (AMF) and 25.00 ± 0.87 min (AMF + 0.05 % LML). Melting enthalpies (ΔH) of AMF were significantly higher (p < 0.05) than the ones observed for AMF + 0.05 % LML when crystallized without HIU, while enthalpy values increased significantly in AMF + 0.05 % LML samples when crystallized with HIU reaching similar values to the ones obtained for AMF without LML. The viscosity of AMF significantly decreased (p < 0.05) on addition of 0.05 % LML and significantly increased on HIU application.     

Cyclic FA monomers in high-oleic acid sunflower oil and extra virgin olive oil used in repeated frying of fresh potatoes

The measurement of FA profile, polar material, oligomers, oxidized triacylglycerols (OTG), total polyphenols, and cyclic FA monomers (CFAM) was used to evaluate the alteration of a high-oleic sunflower oil (HOSO) and an extra virgin olive oil (EVOO) used in 75 domestic fryings of fresh potatoes with frequent replenishment (FR) of unused oil. CFAM were absent in the unused EVOO but appeared in small amounts in the unused HOSO. Although polar material, oligomers, OTG, and CTAM contents increased and linoleic acid and polyphenols content decreased in both oils during repeated frying, the changes produced should be considered small and related to the use of very stable oils and FR. Throughout the 75 fryings, the total CFAM concentration was higher in HOSO than in EVOO. OTG increased more quickly in EVOO, whereas oligomers increased more quickly in HOSO. Polar material and oligomer content appear significantly correlated (r=0.9678 and r=0.9739, respectively; for both, P<0.001) with the CFAM content. A 25% polar material and 12% oligomer content would correspond to about 1 mg·kg⁻¹ oil of CFAM. Data suggest that both oils, particularly EVOO, perform very well in frying, with a low production of oligomers, polar materials, and CFAM.     

Response Surface Analysis and Modeling of Flaxseed Oil Yield in Supercritical Carbon Dioxide

Supercritical fluid extraction of flaxseed oil with carbon dioxide was performed. Effects of particle size, pressure, temperature and the flow rate of supercritical carbon dioxide (SC-CO₂) were investigated. Response surface methodology was used to determine the effects of pressure (30–50 MPa), temperature (50–70 °C) and SC-CO₂ flow rate (2–4 g/min) on flaxseed oil yield in SC-CO₂. The oil yield was represented by a second order response surface equation (R ² = 0.993) using the Box-Behnken design of experiments. The oil yield increased significantly with increasing pressure (p < 0.01), temperature (p < 0.05) and SC-CO₂ flow rate (p < 0.01). The maximum oil yield from the response surface equation was predicted as 0.267 g/g flaxseed for 15 min extraction of 5 g flaxseed particles (particle diameter <0.850 mm) at 50 MPa pressure and 70 °C temperature, with 4 g/min solvent flow rate. Total extraction time at these conditions was predicted as 22 min.     

Influence of the Rancimat Apparatus Operating Parameters on Oxidative Stability Determination of Cold-Pressed Camelina and Hemp Seed Oil

The study investigates the impact of operating parameters such as temperature (90, 100, 110, 120 °C), airflow rate (10, 15, 20 L h⁻¹), and sample weight (3, 6, 9 g) on the oxidative stability of cold-pressed camelina and hemp seed oils using the Rancimat apparatus. Conducted analysis indicates a significant influence of temperature on oils' induction time. Moreover, higher airflows should be selected at high analysis temperatures. Based on the calculated parameters of the oxidation kinetics, it was shown that hemp oil has higher activation energy values than camelina oil. Response surface methodology (RSM) indicates that to minimize the determination time of camelina oil oxidation, the following analysis conditions should be selected: sample weight (SW) = 33.5 g, airflow (AF) = 20 L h⁻¹, and temperature (T) = 120 °C. However, for hemp oil, these parameters should be SW = 5.56 g, AF = 15 L h⁻¹, T = 120 °C. Sample mass does not significantly impact oils induction time, which depends mainly on the temperature and airflow. Practical applications: The conducted research shows that the parameters of the cold-pressed camelina and hemp oils oxidative stability have to be determined experimentally. The determined parameters for assessing the oxidative stability will reduce the analysis time and the possibility of interpolating the obtained result at different temperatures and analysis parameters.     

The effect of supercooling on crystallization of cocoa butter-vegetable oil blends

The solid fat content (SFC), Avrami index (n), crystallization rate (z), fractal dimension (D), and the pre-exponential term [log(γ)] were determined in blends of cocoa butter (CB) with canola oil or soybean oil crystallized at temperatures (T _Cr) between 9.5 and 13.5°C. The relationship of these parameters with the elasticity (G′) and yield stress (σ^*) values of the crystallized blends was investigated, considering the equilibrium melting temperature (T _M ^o) and the supercooling (i.e., T _Cr ^o−T _M ^o) present in the blends. In general, supercooling was higher in the CB/soybean oil blend [T _M ^o=65.8°C (±3.0°C)] than in the CB/canola oil blend [T _M ^o=33.7°C (±4.9°C)]. Therefore, under similar T _Cr values, higher SFC and z values (P<0.05) were obtained with the CB/soybean oil blend. However, independent of T _Cr TAG followed a spherulitic crystal growth mechanism in both blends. Supercooling calculated with melting temperatures from DSC thermograms explained the SFC and z behavior just within each blend. However, supercooling calculated with T _M ^o explained both the SFC and z behavior within each blend and between the blends. Thus, independent of the blend used, SFC described the behavior of G′_eq and σ^* and pointed out the presence of two supercooling regions. In the lower supercooling region, G′_eq and σ^* decreased as SFC increased between 20 and 23%. In this region, the crystal network structures were formed by a mixture of small β′ crystals and large β crystals. In contrast, in the higher supercooling region (24 to 27% SFC), G′_eq and σ^* had a direct relationship with SFC, and the crystal network structure was formed mainly by small β′ crystals. However, we could not find a particular relationship that described the overall behavior of G′_eq and σ^* as a function of D and independent of the system investigated.     

Antagonism of croton oil inflammation by topical emu oil in CD-1 mice

Emu oil is derived from the emu (Dromaius novaehollandiae), which originated in Australia, and has been reported to have anti-inflammatory properties. Inflammation was induced in anesthetized CD-1 mice by applying 50 μL of 2% croton oil to the inner surface of the left ear. After 2 h, the area was treated with 5μL of emu, fish, flaxseed, olive, or liquified chicken fat, or left untreated. Animals were euthanized at 6 h postapplication of different oils, and earplugs (FP) and plasma samples were collected. Inflammation was evaluated by change in earlobe thickness, increase in weight of EP tissue (compared to the untreated ear), and induction in cytokines interleukin (IL)-1α and tumor necrosis factor-α (TNF-α) in EP homogenates. Al-though reductions relative to control (croton oil) were noted for all treatments, auricular thickness and EP weights were, significantly reduced (−72 and −71%, respectively) only in the emu oil-treated group. IL-1α levels in homogenates of auricular tissue were significantly reduced in the fish oil (−57%) and emu oil (−70%) groups relative to the control group. The cytokine TNF-α from auricular homogenates was significantly reduced in the olive oil (−52%) and emu oil (−60%) treatment groups relative to the control group. Plasma cytokine levels were not changed by croton oil treatment. Although auricular thickness and weight were significantly correlated with each other (r=0.750, P<0.003), auricular thickness but not weight was significantly correlated with cytokine IL-1α (r=0.750, P<0.006) and TNF-α (r=0.690, P<0.02). These studies indicate that topical emu oil has anti-inflammatory properties in the CD-1 mouse that are associated with decreased auricular thickness and weight, and with the cytokines IL-1α and TNF-α.     

Interesterification of tea seed oil and its application in margarine production

Blends of hydrogenated and nonhydrogenated tea seed oil (Lahijan variety) (30:70, w/w) were chemically interesterified at 60, 90, and 120°C for 30, 60, and 90 min in the presence of 1% (w/w) NaOH. Physicochemical properties of the products were compared with those of the noninteresterified mixture. Statistical comparison of m.p., iodine values (IV), and solid fat contents (SFC) showed that the sample having the highest ranking was interesterified at 120°C for 30 min. The sample was used as a hardstock (40%), with liquid tea seed oil and sunflower oil (ratios of 100:0, 80:20, 60:40, 40:60, 20:80, and 0:100) as, a softstock (60%) for production of table magarine, and the properties of these margarines were compared with those of commercial ones. Samples E and D (ratio of 80:20 and 60:40 liquid tea seed oil/sunflower oil, respectively) had the lowest significant differences with commercial table margarine for physicochemical (m.p., IV, and SFC) and organoleptic characteristics, respectively. Generally, based on m.p. and SFC, margarines E and D were classified as soft margarine. The trans FA content of E, D, and commercial margarines were 1.8, 1.8, and 2.2%, respectively.     

Influence of Zataria multiflora Boiss. essential oil on oxidative stability of sunflower oil

In this study, the influence of the application of 0.025%, 0.05% and 0.075% of Zataria multiflora Boiss. essential oil (EO) on oxidative stability of sunflower oil was examined and the EO was compared to butylated hydroxyanisole (BHA) and butylated hydroxytoluene (BHT) during storage at 37°C and 47°C. The main components of EO were identified as carvacrol (45.6%), p‐cymene (18.1%) and thymol (16.3%). Peroxide value (PV), anisidine value (AnV) and thiobarbituric acid (TBA) value measurement in sunflower oil showed that all concentrations of EO had a lower antioxidant effect in comparison to BHA and BHT. Samples supplemented with EO concentration of 0.075% were the most stable during storage at both temperatures (p<0.05). Furthermore, Totox value, antioxidant activity (AA), stabilization factor (F) and antioxidant power (AOP) determination confirmed efficacy of this EO as antioxidant in sunflower oil. EO also was able to reduce the stable 2,2‐diphenyl‐1‐picrylhydrazyl free radical (DPPH ^. ) with a 50% inhibition concentration (IC₅₀) of 34.3 ± 0.8 µg/mL. The results indicate that EO could be used as a natural antioxidant in oils for food uses.     

Effect of scraped-surface tube cooler temperatures on the physical properties of palm oil margarine

The effects of scraped-surface tube cooler temperatures on the isothermal solid fat content (SFC) of palm oil margarine during processing and on margarine consistency (yield value, g/cm²), SFC, and polymorphic changes in storage were studied. SFC was measured in the mixing tank after leaving the tube cooler and the pin worker. The SFC at the tube cooler exit was proportional to the amount of cooling; a higher SFC was produced by more extreme cooling treatment. The SFC of all margarines were reduced in the pin worker, and the reduction was related to the initial SFC profile of palm oil. Margarine samples were stored at 28°C for 28 d and tested daily. Margarine processed at 25°C in the tube cooler had the highest consistency and the least change in SFC, but by the second week crystals had transformed into the β form. Uniform product consistency and SFC were observed in margarines processed at 20 and 15°C. These margarines retained the β′ crystal form for 3 and 4 wk, respectively. The best palm oil margarine was obtained with a tube cooler temperature of 15°C and a residence time of 1.8 min.     

Simple Wet Rendering Method for Extraction of Prime Quality Oil from Skipjack Tuna Eyeballs

Oil from skipjack tuna (ST) eyeballs is extracted by the wet rendering method at 121 °C for different holding times (5–60 min) using an autoclave. Yield increases as heating time increases up to 20 min (p < 0.05); no further increase is obtained with a longer heating time (p > 0.05). Conversely, acid value and total polar compounds increase. However, peroxide value (PV), thiobarbituric acid reactive substances, and anisidine value (AnV) decrease up to 30 min. No changes in unsaponifiable matter (UM) or conjugated diene (CD) are attained, regardless of heating time. Polar components (PC) increase with heating time (p < 0.05). All oil samples have a high polyunsaturated fatty acids (PUFA) content (40.46–41.00%), with monounsaturated fatty acids (MUFA) and saturated fatty acids (SFA) in the range of 20.94–21.26% and 37.77–38.45%, respectively. PUFA content is reduced slightly with a heating time of 60 min. Docosahexaenoic acid (DHA) (C22:6, n3) is the dominant fatty acid in all samples (31.67–32.24%). Based on FTIR spectra, heating for longer time results in lower intensity at wavenumbers of 3015 and 1740 cm^?1. Thus, light yellow oil from ST eyeballs prepared by a green process for an appropriate time can serve as an excellent source of DHA and other PUFA. Practical Applications: Tuna oil is known to be a rich source of DHA and PUFA with health benefits. However, precooked tuna heads, generally used as raw material, yield oils with a very dark color and offensive odor, which require several refinery processes. To reduce the number of steps in the refinery process, tuna eyeballs which are separated from tuna heads can render higher quality fish oil. Moreover, the wet rendering process, a green process without toxic substances, can be used without causing environmental problems.     

The influence of chemical interesterification on physicochemical properties of complex fat systems 1. Melting and crystallization

The effects of blending palm oil (PO) with soybean oil (SBO) and lard with canola oil, and subsequent chemical interesterification (CIE), on their melting and crystallization behavior were investigated. Lard underwent larger CIE-induced changes in triacylglycerol (TAG) composition than palm oil. Within 30 min to 1 h of CIE, changes in TAG profile appeared complete for both lard and PO. PO had a solid fat content (SFC) of ∼68% at 0°C, which diminished by ∼30% between 10 and 20°C. Dilution with SBO gradually lowered the initial SFC. CIE linearized the melting profile of all palm oil-soybean oil (POSBO) blends between 5 and 40°C. Lard SFC followed an entirely different trend. The melting behavior of lard and lard-canola oil (LCO) blends in the 0–40°C range was linear. CIE led to more abrupt melting for all LCO blends. Both systems displayed monotectic behavior. CIE increased the DP of POSBO blends with ≥80% PO in the blend and lowered that of blends with ≤70% PO. All CIE LCO blends had a slightly lower DP vis-à-vis their noninteresterified counterparts.     

Investigation of hotpot oil based on beef tallow and flavored rapeseed oil in commercial hotpot seasoning

This study aimed to investigate the quality of hotpot oil from various hotpot seasonings. For this, 12 representative hotpot seasonings with beef tallow (BT) and flavored rapeseed oil (FRO) were collected before the hotpot oil was extracted. The oil content, sensory evaluation scores, physiochemical properties, fatty acid composition, harmful substances, and nutrient content of the hotpot oil were subsequently analyzed. The results showed that the oil content of the hotpot seasoning was 38.3%–58.2%. Furthermore, the BT hotpot oils produced better sensory scores (7–8.5), and their oxidative stability (12.08–13.17 h) was higher on average than that of the FRO hotpot oils. Additionally, the FRO hotpot oils had higher contents of unsaturated fatty acid (81.70%–97.32%), phytosterol (3466.07–6110.37 ppm), tocopherol (182.91–1276.17 mg kg⁻¹), and polyphenol (34.48–61.94 mg kg⁻¹). The factor analyses revealed that the FRO and BT hotpot oils were significantly different and were affected by the iodine value, acid value, and linoleic acid and phytosterol contents. Practical applications: It is necessary to improve the nutritional value and taste of hotpot oils to facilitate rapid development in the hotpot seasoning industry. This study showed FRO was a positive mediator of antioxidant, anti-inflammatory, and anticancer effects owing to its richness of nutritional compounds, such as polyphenols, phytosterols, and tocopherols. In comparison, BT was found to have a lower nutritional value than FRO but added a unique taste and aroma to the hotpot. The use of blended oil as raw oil could also improve the quality of hotpot oil. This information will provide an important guide to the nutritional value and industrial production of hotpot oil. Blended oil is a promising raw oil for future use in hotpot seasoning processing to meet consumer demands for nutritious and pleasantly flavored hotpot oil.     

Heated fat-based oil substitutes, oleic and linoleic acid-esterified propoxylated glycerol

Four oils [triolein, trilinolein, oleic acid-esterified propoxylated glycerol (EPG-08 oleate), and linoleic acid-esterified propoxylated glycerol (EPG-08 linoleate)], each without added antioxidants, were heated for 12 h/d at approximately 190°C in a small deep-fat fryer until the polymer concentration exceeded 20%, as determined by high-performance size-exclusion chromatography. Increases in the free fatty acid content, total acid value, food oil sensor value, and p-anisidine value during heating indicated that significant thermal oxidation had occurred in each oil. Capillary supercritical fluid chromatography (SFC) was used to determine the substrate concentration of each oil after each heating interval. The average, apparent first-order reaction rate constant (as determined by SFC) for trilinolein was 0.0348±0.0034 h⁻¹, while the rate for EPG-08 linoleate was 0.0253±0.0032 h⁻¹. The average apparent reaction rate constant for triolein was 0.0256±0.0011 h⁻¹, while the rate for EPG-08 oleate was 0.0252±0.0008 h⁻¹. Triolein contained >20% polymer after 60 h of heating, EPG-08 oleate contained >20% polymer after 36 h of heating, and both trilinolein and EPG-08 linoleate contained >20% polymer after 24 h of heating.     

Tailoring Crystalline Structure Using High-Intensity Ultrasound to Reduce Oil Migration in a Low Saturated Fat

The objective of this study was to use high-intensity ultrasound (HIU) to change the crystalline structure of an interesterified soybean oil (IESBO) with 33% of saturated fats and to evaluate how these changes affect oil migration. The IESBO was crystallized at different temperatures (26, 28, 30, and 32 °C) with and without HIU. Results show that oil migration was significantly affected by HIU (P < 0.05). HIU promoted crystallization and induced the formation of harder crystalline networks that were more resistant to oil migration with lower melting peak temperatures and sharper melting profiles. Samples processed with HIU had fewer crystalline clusters as observed by microscopy. Changes observed on the physical properties of the IESBO due to sonication that consequently improved oil migration were attributed to the ability of HIU to induce secondary nucleation and crystallize low-melting point triacyclglycerols (SUU) that would not crystallize without the HIU and to the stronger and stable crystalline network formed capable of entrapping liquid TAG (UUU).