Refining,bleaching and hydrogenating meat fats

Meat fats are most often steam refined. This has been the accepted practice for at least 35 years. Meat fats are caustic refined for a few specialized products. The caustic refining conditions differ from those used for vegetable oils primarily in the amount of mixing used after the addition of caustic. Bleaching of meat fats is accomplished easily. Most meat fats are light in color and require clarification more than bleaching. The green color of tallows containing large amounts of chlorophyll is easily removed with activated earth. Meat fats are hydrogenated to develop the SFI curves needed for various products and also are hydrogenated to saturation for use as plasticizing agents. The hydrogenation of lard and tallow is not as complicated as that of most vegetable oils, because the original fat is more saturated and the reaction has fewer possible routes to follow.     

Interference of polar lipids with the alkalimetric determination of free fatty acid in fish lipids

An examination of the suitability of an alkalimetric method for the determination of free fatty acid (FFA) contents in fats, oils, and lipid extracts was conducted by comparing AOCS method Ca 5a-40 with a method based on a Chromarod-latroscan thin-layer chromatography-flame-ionization detector (TLC-FID) system. The FFA contents determined by the alkalimetric method were consistently higher than the genuine FFA contents obtained by the latroscan TLC-FID method. Phospholipids were found to be the major components that contributed to the alkali-titratable, nongenuine FFA in the total FFA determined alkalimetrically. Contributions from other polar lipid components were smaller, but they dominated as the proportion of phospholipids fell. The other alkali-titratable polar components may include oxidized lipids and their by-products bound to protein fragments. The accurate determination of FFA contents by alkalimetric methods may only be applicable to those commercially refined fats and oils that contain negligible amounts of phospholipids. Corrections for the alkalimetrically determined FFA contents should be made for those fats and oils with relatively high phospholipid contents by correlating the nongenuine FFA contents and the phospholipid contents.     

Fatty acid esters of glycidol in refined fats and oils

Discrepancies in the analysis of 3‐chloropropane‐1,2‐diol (3‐MCPD) esters can be explained by the hypothesis that in some refined oils significant amounts of fatty acid esters of glycidol (glycidyl esters) are present in addition to 3‐MCPD esters. Glycidyl esters were separated from triacylglycerols by gel permeation chromatography (GPC) and detected by gas chromatography‐mass spectrometry (GC‐MS). Six samples of palm oil and palm oil‐based fats were analyzed by GPC and GC‐MS. In chromatograms of all samples, significant peaks, retention time and mass spectra in conformity with self‐synthesized glycidyl palmitate and glycidyl oleate were detectable. Quantification of individual glycidyl esters was not possible because of a lack of pure standards. Concentration of ester‐bound glycidol in different samples of fats and oils was estimated using an indirect difference method. Glycidyl esters could be detected only in refined, but not in crude or native, fats and oils. The highest concentrations were detected in palm oil and palm oil‐based fats. In a palm oil sample, glycidyl ester concentration varied according to different deodorization parameters, temperature, and time, while 3‐MCPD ester concentration was relatively constant, indicating that mitigation of glycidyl esters possibly may be achieved by optimizing refining parameters.     

Untersuchung und Beurteilung von PAK in Speisefetten und -ölen

Investigation and Legal Evaluation of Polycyclic Aromatic Hydrocarbons in Vegetable Fats and Oils The analysis of 40 native and refined commercially available vegetable fats and oils reveals the influence of the environment and the treatment on the contamination with PAHs. Totally refined oils and fats have no or only a low contamination of PAHs whereas grapeseed oil contains PAHs to a high extent. This fact has to be deduced to the old-fashioned drying process of the pressed grapes. The analytical procedure with HPLC and fluorimetric detection was done after alcaline hydrolysis. The PAHs were extracted using the distribution between DMF, cyclohexane and water. The legal evaluation of high contaminated is discussed in regard of national and international regulations.     

Farbe von Ölen

Colour of Oils For many products, particularly edible oils and fats, color is an essential indicator for quality. Today instruments are used to measure the color in oils, fats, fatty acids or other substances. The Tintometer is a subtractive colorimeter, which used red, blue and yellow glass standards. Almost everywhere in the world, the Lovibond color scale is nowadays considered as an accepted means of assigning precise color values to edible oils and fats. But there are also, of course, alternative ways and techniques of determining or measuring color. In recent years, the development of microprocessor-controlled colorimeters has made it possible to automatically measure and compare Lovibond color scale and correlating international standard values pursuant to the CIE System.     

Determination of citric acid in fats

The direct analysis of small amounts (2–50 ppm) of citric acid in refined glyceride oils and fats is described. Fat, containing citric acid, is titrated potentiometrically in a pyridine/ acetone mixture with tetrabutylammonium hydroxide (TBAH). The method is relatively simple and rapid with an accuracy better than ±5%.     

Atomic absorption spectroscopy

Atomic absorption spectrophotometry has been used for the rapid determination of various metallic and nonmetallic elements in crude and refined vegetable oils and in animal fats, many present in levels of parts per million. Various types of crude and refined vegetable oils were analyzed for Ca, Cu, Fe, Mg, Mn, P and Zn. This method of analysis has proven to be less time consuming, as accurate and more convenient than other spectroscopic techniques for elemental analyses. Presented at the AOCS-AACC Joint Meeting, Washington, D.C., April, 1968. So. Utiliz. Res. Dev. Div., USDA, ARS.     

Comparison of various analytical techniques for the determination of essential fatty acids in hardened fats

In partially hydrogenated fats containing residual linoleic acid, linoleic acid isomers are found which have no essential fatty acid activity but contribute to the C-18 diene acid values; i.e., to the so-called linoleic acid values obtained by the usual physicochemical methods. Such hydrogenated fats and oil blends, particularly margarine oils, have now been analyzed by a biochemical procedure in the attempt to measure specifically the essential fatty acid content by a direct method. The latter procedure makes use of a lipoxidase enzyme specific for thecis, cis, methylene interrupted diene structure in polyunsaturated fatty acids having two or more double bonds. It is concluded that the biochemical method is equally as reliable as the combined use of the spectrophotometric and thiocyanometric procedures for estimating with precision the essential fatty acid content of hydrogenated fats containing residual dienes; the simplicity and speed of the biochemical method make it the procedure of choice.     

Determination of citric acid and its decomposed products in edible oils by gas liquid chromatography

A quantitative gas liquid chromatographic (GLC) method for four organic acids-citric, aconitic, itaconic, and citraconic acids-in refined oils and fats was developed. After the organic acids are extracted with water from soybean oils, the extract is esterified with n-butanol and an aliquot of the ester is subjected to GLC on a temperature-programmed 10% DEGS column equipped with a flame ionization detector. At 20 and 30 ppm levels, recoveries of the acids from the oil varied from 95 to 100% except for itaconic acid. Citric acid content in commercial edible oils in Japan was from trace to 16 ppm. However, aconitic, itaconic, and citraconic acids were not detected.     

Relative nutritional value of various dietary fats and oils

The dietary and nutritional role of fats and oils is quite complex, as evident in the new biological findings about some of their components that are essential to man. Fats and oils must be considered for both their quantitative and qualitative aspects, their fatty acid compositions and relationships with average diets in different countries should be emphasized. Because of some adverse physiological effects ascribed to saturated fatty acids, a tendency to increase the intake of polyunsaturated vegetable oils has occurred to provide a good source of essential fatty acids, mainly linoleic acid. However, saturated fats still are an important part of the diet in developed countries, especially “invisible” fats. Research must continue that is related to modifications fats and oils undergo during industrial processes which affect their nutritional value. Compositions of many fats and oils are provided.     

Probleme der physikalischen Raffination von Sojaöl

Problems of Physical Refining of Soya Bean Oil The importance of physical refining - above all of palm oil - has permanently increased in the last years. Other oils and fats like for example soya bean oil are more and more refined by this alternative method, too. The report demonstrates the development up to now and the situation of today. The problems of the procedure are explained and a critical estimation is attempted.     

Improved method for quantitating and obtaining the unsaponifiable matter of fats and oils

A quantitative method for saponifying and isolating the unsaponifiable matter (UM) from fats and oils is detailed. The method, which is a modification of a previously described procedure, is faster, uses about half the solvent, and is easier to execute. The minimum time needed to completely saponify a large number of fats and oils is established and conditions for removing contaminating soap from the extracted UM are described. Evidence presented shows some fats and oils to be incompletely saponified using previously indicated time-temperature conditions. The method compares favorably with the AOAC method, but is not applicable to the analysis of marine oils.     

A rapid method for the quantification of fatty acids in fats and oils with emphasis on <Emphasis Type="Italic">trans</Emphasis> fatty acids using fourier transform near infrared spectroscopy (FT-NIR)

A rapid method was developed for classifying and quantifying the FA composition of edible oils and fats using Fourier Transform near infrared spectroscopy (FT-NIR). The FT-NIR spectra showed unique fingerprints for saturated FA, cis and trans monounsaturated FA, and all n−6 and n−3 PUFA within TAG to permit qualitative and quantitative comparisons of fats and oils. The quantitative models were based on incorporating accurate GC data of the different fats and oils and FT-NIR spectral information into the calibration model using chemometric analysis. FT-NIR classification models were developed based on chemometric analyses of 55 fats, oils, and fat/oil mixtures that were used in the identification of similar materials. This database was used to prepare three calibration models—one suitable for the analysis of common fats and oils with low levels of trans FA, and the other two for fats and oils with intermediate and high levels of trans FA. The FT-NIR method showed great potential to provide the complete FA composition of unknown fats and oils in minutes. Compared with the official GC method, the FT-NIR method analyzed fats and oils directly in their neat form and required no derivatization of the fats to volatile FAME, followed by time-consuming GC separations and analyses. The FT-NIR method also compared well with the official FTIR method using an attenuated total reflectance (ATR) cell; the latter provided only quantification of specific functional groups, such as the total trans FA content, whereas FT-NIR provided the complete FA profile. The FT-NIR method has the potential to be used for rapid screening and/or monitoring of fat products, trans FA determinations for regulatory labeling purposes, and detection of contaminants. The quantitative FT-NIR results for various edible oils and fats and their mixtures are presented based on the FT-NIR model developed.     

50 Jahre Technologie pflanzlicher Öle und Fette - ein Erfahrungsbericht

50 Years Technology of Vegetable Oils and Fats - a Report of Experiences In a survey about the development of the technology of vegetable oils and fats between 1932 and 1982 above all those areas are dealt, in which the author could contribute to the optimization of technological process steps and to the quality improvement of final products. It is described in detail: influence of solvent composition on benzine losts and on hydrocarbon retention in the oil seed extraction, improvement of the lecithin removal process, the entire desliming of extracted oils and its influence on raffinate quality, methods for determination of refining lost and for estimation of quality of raw and refined oils, comparison between various alkali-neutralization methods, relations between bleaching earth activity and oxidation stability of the oils, recovery of oil from used bleaching earth, distillative neutralization and determination of optimal deodorising conditions. The report is finished with hints on the importance of special fats for the fat processing industry obtained by hydrogenation, interesterification or fractionation.     

Analysis of sterol content and composition in fats and oils by capillary-gas liquid chromatography using an internal standard. Comments on the German sterol method

The advantages and disadvantages of various approaches to the capillary-gas liquid chromatography (GLC) of sterols in fats and oils with internal standards are discussed. The German method F-III 1²(,3) for sterol analysis in fats and oils, which uses betulin as an internal standard, was reformulated and translated. A number of further improvements and alterations were also made, and the procedure used is described more precisely below in English in order to give detailed explanations, e.g. regarding the role of the aluminium oxide column and of the internal standard betulin. The method is applicable to a wide range of oils and fats, including mixtures of vegetable and animal fats, cereal lipids, and partially hydrogenated fats.     

Principles of palm olein fractionation: a bit of science behind the technology

Dry fractionation is a well‐established and versatile fat modification technology that can produce a broad spectrum of edible oils and fats. Due to its specific chemical composition, especially palm oil can be processed by this technology into fractions that serve as salad oils, frying oils, margarine fats. Whereas the first step of this multi‐stage production process is well understood, the edible oil industry all over the world is much more often confronted with problems in the second stage of the process, when the liquid palm olein is further fractionated. The process of palm olein crystallization is indeed a lot more difficult to control. This article therefore elaborately explains the main, fundamental causes for this sensitivity of palm olein during the fractional crystallization. It further discusses which and how components present in refined palm olein can be responsible for process instability and how they affect the quality of the end products on an industrial scale. The article also highlights which novelties and innovation in dry fractionation technology are currently under investigation.     

Quality of fried foods with palm oil

The amount of imported palm oil in Japan during the past few years has been 140,000–150,000 tons per year, or about 9% of the total consumption of vegetable oils in Japan. In 1975, part of the palm oil was imported as refined type from Malaysia. At the present time, almost all of the palm oil from Malaysia is refined. At the starting point quality of the refined palm oil was not so good, but today it is fairly improved by efforts of Malaysian processers. Palm oil has excellent properties against oxidation, and it has been generally accepted by consumers as a vegetable oil for health foods. There also is a big potential for increasing consumption of palm oil in fried foods. Severe regulation of food additives restricts the use of artificial antioxidants and therefore strict quality control is required to get stable frying oils. Consumer knowledge of foods is increasing, and our responsibility for making good quality frying fats is very important.     

Choice of Simple Methods for Quality Control of Frying Fat during Deep Frying of Potato Products

Studies have been carried out to choice methods which could assess in best way the complex changes in fat during deep frying of French fries and potato crisps. A special emphasis was laid on the estimation of usefulness of simple and quick “methods” which could practically indicate the utilization time of fats (soybean oil, low erucic acid rapeseed oil, ?Sofryt”? -hardened soybean oil), used in deep-fat frying of potato products. Besides the oxidized fatty acid content, proposed by DGF (German Society for Fat Science) as a basic test for the quality assessment of used frying fats, following control tests during the deep-fat frying of potato products have been appointed: colour tests with bromthymol blue and 2,6-dichlorphenol-indophenol, sensoric evaluation, dielectric constant and colour by iodine scale. For these tests suitable limits, qualifying the utility of oils and fats for further frying of French fries and potato crisps, have been estimated.     

Determination of Raffination of Edible Oils and Fats by Olefinic Degradation Products of Sterols and Squalene,Using Coupled LC-GC

Raffination of edible oils and fats, i.e. bleaching with earth or charcoal as well as deodoration, can be determined by the analysis of dehydroxylation products of sterols and isomerization products of squalene. These olefinic degradation products are isolated from the rest of the oil by LC on silica gel and on-line transfer to GC. Sample preparation consists of preparing a 20% solution of the oil. Nearly half of the “extra virgin” olive oils analyzed contained such products, but concentrations were too low for assuming admixture of regularly refined oils. However, many other oils advertized as non-refined turned out to have been treated beyond declaration.