Effect of water washing on the reduction of surface total lipids and FFA on milled rice

A simple method for removing total lipids from the rice surface by water washing is described for brewing operations, where small FFA levels can have a considerable effect on end-product flavor quality. Commercially milled (first-, second-, and third-break) rice was washed with deionized water with constant stirring for 5 and 10 min. About 60 to 80% of total surface lipids were removed by water washing, with a reduction of FFA and conjugated dienes (CD) relative to unwashed control samples. The total surface FFA content of first-, second-, and third-break milled rice was reduced by more than 50% of the original value by washing. Increases in FFA and CD in washed rice after 7 d of storage at 37°C and 70% RH were much lower than those of unwashed controls, in which FFA and CD development was considerably greater and reached brewing quality. Water washing may be a practical means of reducing off-flavor development in milled rice.     

Lipid hydrolysis and oxidation on the surface of milled rice

The changes in milled rice FFA content and composition and in conjugated diene (CD) content and bacterial, yeast, and mold counts were determined at 24, 37, and 50°C and 70% RH over 50 d. There was a rapid rate of FFA formation during the first few days of storage, which was optimal at 37°C, but that slowed after 2, 4, and 5 d at 37, 24, and 50°C, respectively. There was a second increase in FFA after about day 12 that increased with increasing temperature, indicating nonlipase hydrolysis. Linoleic and oleic acids were the main components of the total FFA produced on the surface of milled rice. The pattern of CD development followed that of FFA increase. Bacterial growth correlated with increased FFA levels after 12 d of storage, suggesting that bacterial lipase rather than bran lipase may be responsible for rice lipid hydrolysis     

Hydrolysis of acylglycerols and phospholipids of milled rice surface lipids during storage

The relative contribution of acylglycerols and phospholipids to the lipid hydrolysis in milled rice was investigated during storage at 37°C and 70% RH for 50 d. The MAG, DAG, and lysophospholipid contents of surface lipid were determined by reversed-phase HPLC. The MAG and DAG content of milled rice increased during storage from 0.06 to 0.18% (w/w milled rice), with the MAG content increasing more than that of the DAG. Lysophosphatidylcholine increased throughout the study from 0.013 to 0.034% (w/w), whereas lysophosphatidylinositol and lysophosphatidylethanolamine contents initially increased from 0.002 to 0.003% and from 0.005 to 0.009% (w/w), respectively, and then stabilized until day 50. The relative percentage of TAG and phospholipids hydrolyzed in milled rice increased rapidly during the first 3 d of storage from 12.3 to 37.6% and 25.0 to 62.5% (w/w), respectively, and steadily increased to 53.1 and 73.8% (w/w) on day 50. A higher percentage (62.5%) of phospholipids was hydrolyzed relative to TAG (37.6%) after 3 d and probably contributed significantly to milled rice lipid hydrolysis during early storage. However, TAG concentration (0.57%, w/w) was much higher relative to phospholipids (0.08%, w/w) in surface lipids, and therefore TAG hydrolysis was the major contributor to FFA development and the quality of stored milled rice.     

Free fatty acid formation and lipid oxidation on milled rice

Milled rice was stored at 37°C and 70% humidity and sampled regularly for 50 d. Rice surface lipid was extracted with isopropanol and analyzed for free fatty acids (FFA) and conjugated diene (CD) contents. Diffuse reflectance Fourier transform infrared (DRIFTS) spectra of the rice samples were also obtained. FFA and CD levels increased together during rice storage and exhibited three distinct phases. DRIFTS identified a decrease in intensity at 1746 cm⁻¹ (ester, −C=O) and increases in intensity at 1731 cm⁻¹ (aldehyde, −CO) and 1714 cm⁻¹ (fatty acid, −C=O) during storage, which correlated well with the chemical analysis data. DRIFTS spectral data were analyzed by a partial least squares regression method to identify spectral regions that correlate strongly with measured FFA and construct prediction models. Overall, the mid-infrared region (4000–400 cm¹) gave the best model (R=0.98, root mean square error of cross-validation=0.05) and also predcted the FFA content of milled rice well. The DRIFTS technique has potential for use in studying qualitative chemical changes on the milled rice surface lipids and for predicting FFA on milled rice.     

预处理稻壳及其与杨树锯末掺混燃烧特性和燃烧动力学分析

采用热重技术对稻壳（DK）和杨树锯末（JM）燃烧进行分析,考察了不同预处理方式对稻壳燃烧特性的影响,并研究了不同升温速率及稻壳和杨树锯末掺混质量比对掺混燃烧特性及燃烧动力学的影响。结果表明：水洗及酸洗可使稻壳燃烧TG-DTG热重曲线向高温区移动,最大失重速率及对应失重温度升高。水洗使稻壳综合燃烧特性指数提高2.5×10^-7~5.9×10^-7%/（min²·℃³）,而酸洗使稻壳综合燃烧特性指数下降11×10^-7~11.9×10^-7%/（min²·℃³）。不同预处理后稻壳在挥发分析出燃烧阶段的活化能高于未处理稻壳,酸洗后稻壳焦炭燃烧阶段活化能降低16.94 kJ/mol,而水洗使稻壳焦炭燃烧阶段活化能升高。提高稻壳添加比例,混合燃料着火温度和燃尽温度降低。随着升温速率的提高,混合样品综合燃烧特性指数和残余率升高。70%稻壳和30%杨树锯末混合燃料在升温速率40℃/min下燃烧产生协同效应。     

Interlaboratory study on lipid oxidation during accelerated storage trials with rapeseed and sunflower oil analyzed by conjugated dienes as primary oxidation products

Accelerated storage tests are frequently used to assess the oxidative stability of foods and related systems due to its reproducibility. Various methods and experimental conditions are used to measure lipid oxidation. Differences between laboratories make it necessary to determine the repeatability and reproducibility of oxidation tests performed under the same conditions. The objective of the present interlaboratory study was to evaluate the outcome of a storage test for two different bulk oils, sunflower oil (SFO) and rapeseed oil (RSO), during a period of 9 weeks at 20°C, 30°C, 40°C, and 60°C. Sixteen laboratories were provided with bottled oils and conducted the storage tests according to a detailed protocol. Lipid oxidation was monitored by the formation of conjugated dienes (CD) and the activation energy (E_a) was determined for comparative purposes and statistically evaluated. An increase in CD formation was observed for both oils when the storage temperature was increased in all laboratories. The E_a,1 ranged from 47.9 to 73.3 kJ mol⁻¹ in RSO and from 27.8 to 62.6 kJ mol⁻¹ in SFO, with average values of 58.2 and 46.8 kJ mol⁻¹, respectively. The reproducibility coefficients were 10.9% and 18.2% for RSO and SFO, respectively. Practical applications: In order to compare results on oxidative stability of foods derived from different studies, the reproducibility of storage tests and methods employed to evaluate the oxidation level should be considered. This study provides fundamental data on the reproducibility of lipid oxidation under accelerated storage conditions and defines important parameters to be considered for the conduction of experiments.     

Rice bran FFA determination by diffuse reflectance IR spectroscopy

Rice bran with FFA levels above 0.1% cannot be used as a food ingredient due to oxidative off-flavor formation. However, extracting high FFA oil from bran by in situ methanolic esterification of rice bran oil to produce methyl ester biodiesel produces greater yields relative to low-FFA rice bran oil. Therefore, high-FFA bran could be exploited for biodiesel production. This study describes an FTIR spectroscopic method to measure rice bran FFA rapidly. Commercial rice bran was incubated at 37°C and 70% humidity for a 13-d incubation period. Diffuse reflectance IR Fourier transform spectra of the bran were obtained and the percentage of FFA was determined by extraction and acid/base titration throughout this period. Partial least squares (PLS) regression and a calibration/validation analysis were done using the IR spectral regions 4000-400 cm⁻¹ and 1731-1631 cm⁻¹. The diffuse reflectance IR Fourier transform spectra indicated an increasing FFA carbonyl response at the expense of the ester peak during incubation, and the regression coefficients obtained by PLS analysis also demonstrated that these functional groups and the carboxyl ion were important in predicting FFA levels. FFA rice bran changes also could be observed qualitatively by visual examination of the spectra. Calibration models obtained using the spectral regions 4000-400 cm⁻¹ and 1731-1631 cm⁻¹ produced correlation coefficients R and root mean square error (RMSE) of cross-validation of R=0.99, RMSE=1.78, and R=0.92, RMSE=4.67, respectively. Validation model statistics using the 4000-400 cm⁻¹ and 1731-1631 cm⁻¹ ranges were R=0.96, RMSE=3.64, and R=0.88, RMSE=5.80, respectively.     

Rancidity development during the chilled storage of farmed Coho salmon (Oncorhynchus kisutch)

Coho salmon (Oncorhynchus kisutch) is a fatty fish species whose farming production has greatly increased in recent years. Lipid damage produced during Coho salmon chilled storage was studied for up to 24 d. Lipid hydrolysis (free fatty acids, FFA) and oxidation (conjugated dienes; peroxide value, PV; thiobarbituric acid index, TBA‐i; fluorescent compounds formation, FR; browning development) were determined and compared to lipid composition (polyene index, PI; astaxanthin, AX) changes and sensory assessment (rancid odour development) results. Most lipid damage indices developed slowly during storage; thus, values obtained for FFA, PV, TBA‐i and FR were in all cases under 1.5 g/100 g, 4.0 meq oxygen/kg lipid, 0.40 mg malondialdehyde/kg muscle and 0.40, respectively. Odour assessment showed a significant (p <0.05) rancidity development at day 10, when compared to starting fish material; then, non‐acceptable values were obtained at days 19 and 24. The PI analysis showed not many differences during the storage time, with the lowest mean value at day 19. AX analysis indicated a relatively high content in the white muscle, which was maintained till the end of the experiment. A low oxidation development is concluded for Coho salmon lipids when compared to other fatty fish species under the same chilling conditions. AX was found to contribute to the oxidation stability of Coho salmon lipids, due to its free radical scavenger properties.     

Fatty acid composition and oxidation of lipids in Korean catfish

This study determined the lipid content and FA composition of muscle and a mixture of muscle and viscera from Korean catfish as well as lipid oxidation and hydrolysis. Lipid content and FA compositions in Korean catfish, which were purchased every month or two during September 1999–July 2000, were analyzed. Lipid oxidation and hydrolysis were determined as PV, thiobarbituric acid value, and FFA in the muscle and the mixture during storage at 2°C for 12 d and −14°C for 9 wk. Lipid contents of the muscle and the mixture were 3.2 (w/w) and 5.4%, respectively. Oleic acid was the most abundant FA in the catfish lipids, constituting 28.0% (w/w) of total FA in the muscle and 25.6% in the mixture, followed by palmitic acid and linoleic acid, amounting to 20.2 and 12.2%, respectively, in the muscle and 20.2 and 12.5% in the mixture. EPA and DHA were 3.2 and 6.8%, respectively, in the muscle and 3.5 and 8.1% in the mixture. Seasonal variation in lipid contents and FA composition was minimal in catfish. Lipids in minced catfish oxidized and hydrolyzed readily at 2°C. Inclusion of viscera into the muscle increased lipid oxidation and hydrolysis. Frozen storage at −14°C and addition of ascorbic acid both reduced lipid oxidation. Frozen storage retarded lipid hydrolysis in catfish.     

Influence of blanching treatment and drying methods on the drying characteristics and quality changes of dried sardine (Sardinella gibbosa) during storage

The aim of this study is to examine the drying characteristics of blanched and unblanched sardine during indoor and open sun drying processes. Changes in temperature and relative humidity of the air during drying were recorded. The color, peroxide value (PV), thiobarbituric acid reactive substances (TBARS), free fatty acid (FFA) content, fatty acid composition, and sensory attributes of dried samples were also evaluated once a month for 5 months of storage. High drying rates were obtained in all samples at the start of drying and then decreased with increasing drying time. The highest drying rate and effective water diffusivity (D_eff) were observed in blanched sardine during open sun drying. Blanching treatment slowed down the FFA progression during product storage but adversely affected the color, PV, and TBARS content as well as sensory properties. Although sardine dried for a longer time under indoor drying conditions, it attained a stable moisture ratio that was lower than in open sun-dried samples. Indoor drying produced a quality stable product with less lipid oxidation and the desired moisture content, higher polyunsaturated fatty acids and sensory properties. Blanching treatment negatively affected the fish quality and is therefore not recommended for commercial sardine drying.     

Initial activation of platinum-rhodium gauzes for the catalytic oxidation of ammonia

Studies have been made of the activation of platinum-rhodium gauze catalysts for the oxidation of ammonia, using optical microscopy, electron probe microanalysis (EPMA), and electron spectroscopy to characterize the surfaces. The initial washing procedure is found to remove calcium and to reduce carbon residues on the surface, as a result of which the catalyst is active at lower temperatures. Subsequent activation in a hydrogen flame or in oxygen causes surface rearrangements and results in rhodium enrichment at the surface: this latter trend is partially reversed in the early stages of the oxidation of ammonia. Water vapor is found to deactivate the activated gauze.     

Effects of drying methods and enzyme aided on the fatty acid profiles and lipid oxidation of rice by-products

We investigated the influence of hot air drying, far infrared radiation (FIR), and cellulase aided on the fatty acid composition and primary lipid oxidation of rice bran, rice husk, and ground rice husk. The lipid content was significantly reduced in the sample dried by hot air and FIR but remained unchanged in the cellulase-aided rice bran and husk. We found that oleic acid (18:1n ? 7) and linoleic acid (18:2n ? 6) increased in hot air- and FIR-dried rice bran. On the other hand, PUFA content was significantly reduced in the samples dried by hot air and FIR but remained unchanged in the cellulase-aided rice bran and husk. Cellulase aided gave significantly higher concentrations of SFA, MUFA, and PUFA in all samples than did hot air and FIR drying. However, the rice by-products dried with hot air and FIR had the lowest PV and TBA values during 30 days of storage. Our findings provide useful information for the pretreatment of rice by-products; consequently, more utilization of rice by-products will be extended for uses such as oil production.     

Lipid damage during frozen storage of Gadiform species captured in different seasons

Quality loss of two gadiform fish species (blue whiting, Micromesistius poutassou; hake, Merluccius merluccius) during frozen storage (–30 and –10 °C; up to 12 months) was studied. For this, hydrolytic (formation of free fatty acids, FFA) and oxidative (conjugated dienes, peroxide and interaction compound formation) lipid damage were analysed. For both species, individual fishes captured in two different trials (May and November) were considered. Increasing (p <0.05) lipid hydrolysis and oxidation (peroxide and interaction compound formation) were observed for all kinds of samples throughout the frozen storage. Interaction compound detection by fluorescence analysis showed the best correlation values with storage time. Some higher (p <0.05) hydrolysis development could be observed in hake captured in May than in its counterpart from the November trial, while frozen blue whiting did not provide definite differences for FFA formation between both trials. Concerning peroxide formation, higher (p <0.05) values were obtained for individual blue whiting and hake captured in November when compared to their corresponding May fish for both frozen storage conditions. Interaction compound formation was also found to be higher (p <0.05) for November hake fish than for its counterpart captured in May, while blue whiting did not provide definite differences between trials.     

Fatty acid evolution during the storage of ground,roasted coffees

During storage, the quality of coffee decreases, partially because coffee lipids degrade by lipolysis and oxidation. The aim of this study was to compare the evolution of the fatty acid (FA) profile in two ground, roasted coffees—Brazilian Arabica 100% (A100), and a blend of Brazilian Arabica 80% and Indian Cherry Robusta 20% (A80/R20)—throughout 180 d of storage. Linoleic acid (40.1% in A100, 40.2% in A80/R20) and palmitic acid (36.4% in both samples) were the main total FA. No significant change in the FA profile was observed throughout the storage period. A significantly higher total free fatty acid (FFA) initial concentration appeared in A80/R20 coffee (1108.5 mg/100 g fat) compared with A100 coffee (730.2 mg/100 g fat). Except for the first week of storage, similar FA oxidation patterns were found for both coffees, but FFA generation was faster in the A80/R20 blend than in A100.     

Effect of airflow rate on drying air and moisture content profiles inside a cross-flow drying column

Rice at 20.5 and 16.3% initial moisture contents (IMCs) was dried using 57°C/13% RH air at airflow rates (Qs) of 0.36, 0.46, and 0.56 (m³/s)/m² for 30, 60, and 90?min, respectively, in an experimentally simulated cross-flow drying column. Q significantly affected the drying air and rice moisture content profiles within the drying column; for a particular drying duration, the range of MCs within the column decreased as Q increased. Q also impacted the extents of intra-kernel material state gradients created and thus had potential impacts on kernel fissuring and consequent head rice yield reduction. In addition, the impact of Q on the above-mentioned profiles was dependent on the rice IMC.     

FA monoalkylesters from rice bran oil by <Emphasis Type="Italic">in situ</Emphasis> esterification

Extraction and in situ esterification of rice bran oil with ethanol were investigated by studying the effects of rice bran oil FFA content and water content of ethanol. Ethyl ester formation in the ethanol phase increased as FFA content increased. Neutral oil solubility in this phase fell considerably, resulting in a high ethyl ester content. The decrease of the water content in ethanol led to an increase in neutral oil solubility in ethanol and promoted the equilibrium of reaction to ethyl-ester formation, resulting in lower FFA content of the product. The main factor that affected yield and monoester content when using high-acidity bran and various monohydroxy alcohols was the solubility of neutral oil in alcohol. The highest monoester content was obtained with methanol.     

DYNAMIC OPTIMAL CONTROL OF BATCH RICE DRYING PROCESS

The drying of paddy rice may result in quality degradation, expressed as a head kernel yield, leading to significant commercial depreciation of the product. A mathematical model of the drying and of the quality degradation process was combined with a dynamic optimization algorithm to determine the drying conditions (air temperature and relative humidity as functions of time) that ensured the highest possible final product quality for a specified drying time and a specified final moisture content. The robustness of the optimal drying strategy with respect to the initial state of the product, to the model parameters and to the initialization of the optimization algorithm was verified. The compromise between the highest achievable final quality and the allowed total drying time was studied. The combination of simulation and optimization yielded a new insight in the rice drying process and in the quality preservation strategies.     

Effect of droplet size on lipid oxidation rates of oil-in-water emulsions stabilized by protein

In emulsions lipid oxidation is mainly influenced by the properties of the interface. The aim of this work was to investigate the effects of droplet size and interfacial area on lipid oxidation in protein-stabilized emulsions. Emulsions, made of stripped sunflower oil (30% vol/vol) and stabilized by BSA were characterized by surface area values equal to 0.7, 5.1, and 16.3 m²·cm⁻³ oil. The kinetics of O₂ consumption and conjugated diene (CD) formation, performed on emulsions and nonemulsified controls, showed that emulsification prompted oxidation at an early stage. On condition that oxygen concentration was not limiting, the rates of O₂ consumption and CD formation were higher when the interfacial area was larger. Protein adsorbed at the interface probably restrained this pro-oxidant effect. Once most of the O₂ in the system was consumed (6–8 h), CD remained steady at a level depending directly on the ratio between oxidizable substrate and total amount of oxygen. At this stage of aging, the amounts of primary oxidation products were similar whatever the droplet size of the emulsion. Hexanal and pentane could be detected in the headspace of emulsions only at this stage. They were subsequently produced at rates not depending on oil droplet size and interfacial area.     

Influence of ascorbic acid and ascorbyl palmitate on the aroma composition of an oxidized vegetable oil and its emulsion

The formation of conjugated diene hydroperoxides and hexanal was compared to the development of aroma profiles during initial lipid oxidation of a vegetable oil and its 40% oil-in-water emulsion at 60°C. The aroma profiles of the oil and the emulsion with and without addition of ascorbic acid or ascorbyl palmitate were compared. The aroma compounds were isolated under a model mouth system and analyzed by gas chromatography/sniffing port analysis. Detectable odors were found and corresponded to 11 and 14 volatile compounds in the oil and the emulsion, respectively. The emulsion had higher lipid oxidation rates than the oil. Addition of ascorbic acid and ascorbyl palmitate had little influence on the aroma composition of the oil. In the emulsion, addition of these compounds resulted in diminished generation of odor active compounds. Results of measurements of conjugated diene hydroperoxides and headspace hexanal corresponded to that of the lipid oxidation rate in general, but predicted insufficiently the alterations in the aroma compositions by antioxidants.