JP5955119B2 - Method for producing edible fats and oils - Google Patents

Method for producing edible fats and oils Download PDF

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JP5955119B2
JP5955119B2 JP2012135778A JP2012135778A JP5955119B2 JP 5955119 B2 JP5955119 B2 JP 5955119B2 JP 2012135778 A JP2012135778 A JP 2012135778A JP 2012135778 A JP2012135778 A JP 2012135778A JP 5955119 B2 JP5955119 B2 JP 5955119B2
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山本 浩志
浩志 山本
功 中西
功 中西
敦則 熊西
敦則 熊西
紗耶香 東
紗耶香 東
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Ueda Oils and Fats Manufacturing Co Ltd
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この発明は、トランス脂肪酸の生成が低減され、風味、酸化安定性に優れた食用油脂の製造方法に関するものである。   The present invention relates to a method for producing edible fats and oils with reduced production of trans fatty acids and excellent flavor and oxidation stability.

食用油脂は、動植物から採油された原料油に含まれる不純物を取り除く工程、すなわち精製工程を経ることにより、風味や色調を良くして、様々な食品に使用できるようになる。中でも精製の最終工程では、それまでの精製工程で除去しきれなかった、微量な脂肪酸や有臭成分、色素等を取り除くための脱臭と呼ばれる工程が行なわれている。   Edible fats and oils can be used for various foods by improving the flavor and color tone through a process of removing impurities contained in raw material oil collected from animals and plants, that is, a purification process. In particular, in the final purification process, a process called deodorization for removing traces of fatty acids, odorous components, pigments, and the like that could not be removed in the previous purification process is performed.

通常、脱臭の方法としては減圧水蒸気蒸留が採用されており、真空度5hPa前後、温度240〜260℃が主流となっている。   Usually, as a method of deodorization, vacuum steam distillation is adopted, and the degree of vacuum is around 5 hPa and the temperature is 240 to 260 ° C.

食用油脂は様々な食品に使用され、油脂以外の成分の呈味性や色具合を引き出す必要があるため、脱臭後の油はほとんど臭気を感じることがないものとし、淡黄色で極めて無味に近いものが求められてきた。そのため、脱臭温度を高くすることでこの要望に対応してきた。   Edible fats and oils are used in various foods, and it is necessary to draw out the taste and color of ingredients other than fats and oils. Things have been sought. Therefore, this demand has been met by increasing the deodorization temperature.

一方、トランス脂肪酸を過剰に摂取すると、血液中のLDLコレステロールを上昇させると共にHDLコレステロールを低下させて冠動脈心疾患のリスクを高めることが喧伝されるに至り、油脂中のトランス脂肪酸を極力少なくするべき対策が進められてきた。   On the other hand, excessive consumption of trans fatty acids will increase the risk of coronary heart disease by lowering HDL cholesterol and increasing LDL cholesterol in the blood, and should be reduced as much as possible. Countermeasures have been promoted.

トランス脂肪酸の生成において、油脂中に多量に含有させる可能性のある部分水素添加については、水素添加方法の工夫やエステル交換油で代替するなどにより大幅な低減がなされつつある。   In the production of trans fatty acids, partial hydrogenation that may be contained in a large amount in fats and oils is being drastically reduced by devising the hydrogenation method or replacing it with transesterified oil.

しかし、油脂の脱臭工程においても少量ながらトランス脂肪酸が生成する。それにもかかわらず、現状の品質と製造コストを悪化させずにトランス脂肪酸を低減させる食用油の製造方法は知られていない。   However, a small amount of trans fatty acid is also produced in the oil and fat deodorization process. Nevertheless, there is no known edible oil production method that reduces trans fatty acids without deteriorating current quality and production costs.

因みに、トランス脂肪酸は、油脂に対する処理温度が160〜180℃の条件では、ほとんど生成されないことは食品安全委員会の新開発食品評価書「食品に含まれるトランス脂肪酸」で言及されており、脱臭温度を下げれば低減できることは予測できるが、それだけでは、脱臭の本来の目的である不純物や有臭成分の効率的な除去と、天然油脂が有する酸化安定性に寄与する成分の残存を両立させ、しかも現在の安価なコストの範囲内で実現させるための具体的方法とはなりえない。   Incidentally, it is mentioned in the Food Safety Commission's newly developed food evaluation document “Trans Fatty Acids in Foods” that trans fatty acids are hardly produced under the conditions of a processing temperature of 160 to 180 ° C. for oils and fats. It can be predicted that this can be reduced by lowering the value, but that alone can achieve both the effective removal of impurities and odorous components, which are the original purpose of deodorization, and the remaining components that contribute to the oxidation stability of natural fats and oils. It cannot be a concrete method for realizing it within the current low cost range.

また、油脂には二重結合数の異なる種々の脂肪酸が含有されているため、トランス脂肪酸と一口でいってもそれぞれ異性化し易さは大いに異なり、油脂のおかれた様々な条件により変わるので、非常に複雑なことになり、反応速度論的に計算することは困難と考えられ、実質的には不可能である。   In addition, since fats and oils contain various fatty acids with different numbers of double bonds, the ease of isomerization varies greatly depending on the various conditions in which the fats and oils are placed. It would be very complex and would be difficult to calculate kinetically and practically impossible.

食用油の脱臭に係る製造方法としては、脱臭温度230℃、脱臭時間60分間、蒸気吹込量対油5質量%でトランス型脂肪酸含量が2.2質量%になることが、フラックス油で示されている(特許文献1)。   As a manufacturing method related to deodorization of edible oil, it is indicated with flux oil that the trans-fatty acid content is 2.2% by mass when the deodorization temperature is 230 ° C., the deodorization time is 60 minutes, the steam blowing amount is 5% by mass of oil, and 5% by mass of oil. (Patent Document 1).

また、トリエン脂肪酸が40質量%以上の油脂に関して198〜247℃で脱臭した後、脱臭済の第二の油脂とブレンドする方法がある(特許文献2)。   Moreover, there exists the method of blending with deodorized 2nd fats and oils, after deodorizing at 198-247 degreeC regarding the fats and oils whose triene fatty acid is 40 mass% or more (patent document 2).

また、薄膜式カラムとトレイ式装置を組み合わせた精製方法も知られている(特許文献3)。   A purification method combining a thin-film column and a tray-type device is also known (Patent Document 3).

特開2000−157170号公報JP 2000-157170 A 特開2009−79153号公報JP 2009-79153 A 特開2007−14263号公報JP 2007-14263 A

しかし、特許文献1に記載されている脱臭温度230℃、脱臭時間60分間、蒸気吹込量対油5質量%でトランス型脂肪酸含量が2.2質量%になるフラックス油では、トランス脂肪酸が高く、また同特許文献において比較例として記載されている脱臭温度215℃の温度条件では風味、臭気共に不良であるという問題点がある。   However, in the flux oil described in Patent Document 1 with a deodorization temperature of 230 ° C., a deodorization time of 60 minutes, a steam blowing amount with respect to oil of 5% by mass and a trans fatty acid content of 2.2% by mass, the trans fatty acid is high, Moreover, there exists a problem that both flavor and odor are inferior on the deodorizing temperature of 215 degreeC described as a comparative example in the patent document.

また、特許文献2に記載されている方法では、単独の食用油脂を得ることはできず、実施例に示された菜種油やコーン油はトランス脂肪酸がいずれも高いものになるという問題点がある。   Moreover, in the method described in Patent Document 2, it is not possible to obtain a single edible oil and fat, and the rapeseed oil and corn oil shown in the examples have a problem that both of the trans fatty acids are high.

また、特許文献3に記載された方法では、実質的には脱臭方法に関するものであるが、トランス脂肪酸の増加量は0.5%以上であり、油脂の色調も高く、薄膜式カラムとトレイ式装置という2つの装置を用いる必要があるため、工程数が多くコスト的にも有利ではなかった。   The method described in Patent Document 3 is substantially related to a deodorization method, but the increase amount of trans fatty acid is 0.5% or more, the color tone of fats and oils is high, and a thin film column and tray type are used. Since it is necessary to use two apparatuses called apparatuses, the number of processes is large and it is not advantageous in terms of cost.

ところで、マーガリン類やフライ用油脂において、家庭用向けの商品に関しては食感の点から液状油や融点の低い油脂が多く用いられている。   By the way, in margarines and frying fats and oils, liquid oils and fats and oils having a low melting point are often used from the viewpoint of texture for household products.

固形脂のトランス脂肪酸は、概ね0.5%以下に低減させることが可能であるが、二重結合の多い液状油等では脱臭後の精製油脂においてトランス脂肪酸を1%以上含有しており、より一層の低減を図るためには、精製時における特に最終工程の油脂の脱臭工程時に、トランス脂肪酸の生成量を低減させる必要がある。
また、トランス脂肪酸の生成量を充分に低減させ得たとしても、油脂の品質を低下させることは避ける必要があり、また大幅なコスト上昇は産業上受け入れられない。
Although the trans fatty acid of solid fat can be reduced to approximately 0.5% or less, liquid oil with many double bonds contains 1% or more of trans fatty acid in the refined fat after deodorization. In order to achieve further reduction, it is necessary to reduce the amount of trans fatty acid produced during refining, particularly during the final step of deodorizing fats and oils.
Moreover, even if the production amount of trans fatty acid can be sufficiently reduced, it is necessary to avoid a reduction in the quality of fats and oils, and a significant increase in cost is not accepted industrially.

そこで、本願の各請求項に係る発明(以下、本願発明という。)は、上記した問題を解決し、トランス脂肪酸の生成量を従来の精製油脂における生成量よりも充分に低減すると共に、風味や酸化安定性に影響を及ぼす不純物を充分に除去し、しかも酸化安定性や風味安定性を向上させた食用油の製造方法とすることを課題としている。   Accordingly, the invention according to each claim of the present application (hereinafter referred to as the present invention) solves the above-described problems, reduces the production amount of trans fatty acid sufficiently than the production amount of conventional refined oils and fats, It is an object of the present invention to provide a method for producing edible oil that sufficiently removes impurities affecting oxidative stability and improves oxidative stability and flavor stability.

また、食用油脂製造産業における利用価値を高めるため、可及的に簡易で低コストの製造工程とすることも課題である。   In addition, in order to increase the utility value in the edible fat and oil manufacturing industry, it is also a problem to make the manufacturing process as simple and low-cost as possible.

本願の発明者らは、食用油の製造での脱臭工程における、脱臭温度、脱臭時間、水蒸気吹込対油量とトランス脂肪酸の生成量及び精製油の品質を詳細に調べ、トランス脂肪酸が生成しやすい温度領域において、精製油脂の品質が良好であり、特定の温度域では上記3因子が密接に関係しあってトランス脂肪酸の生成量が変動することを見出し、さらに水蒸気吹込対油量を多くするとトランス脂肪酸の生成が抑制されることを見出した。   The inventors of the present application examine in detail the deodorization temperature, the deodorization time, the amount of oil injected with steam, the amount of trans fatty acid produced and the quality of the refined oil in the deodorizing step in the production of edible oil, and the trans fatty acid is likely to be produced. In the temperature range, the quality of the refined fats and oils is good, and in the specific temperature range, the above three factors are closely related, and the amount of trans fatty acid produced varies. It has been found that the production of fatty acids is suppressed.

また、上記3つの因子のバランスをとる所定調整によって、脱臭後の油脂の品質を悪化させることなく、風味や酸化安定性に優れた食用油脂が得られることを見出した。   Moreover, it discovered that edible fats and oils excellent in flavor and oxidation stability could be obtained without deteriorating the quality of the deodorized fats and oils by the predetermined adjustment that balances the above three factors.

さらに、トランス酸を極力生成させないように工夫する過程において、特定の脂肪酸構成を持つ原料油について、前記効果がより顕著に現れることを見出し、本願の各請求項に係る発明を完成させるに至った。   Furthermore, in the process of devising not to generate transacid as much as possible, it was found that the effect appears more remarkably with respect to the feedstock having a specific fatty acid composition, and the invention according to each claim of the present application has been completed. .

具体的には、先ず、大豆油、なたね油について、後述する図1に示すガラス器具を用い、脱臭時間を50分、脱臭中の水蒸気脱臭吹込み対油比率を1%と一定にして脱臭温度を180〜250℃の範囲でいろいろ変えて脱臭油のトランス脂肪酸の生成量を調べた。この脱臭試験時に脱臭温度を横軸(x)、トランス脂肪酸量の生成量を縦軸(y)にプロットしてみると図2に示すものが得られ、脱臭温度が上がるにつれて指数関数的に増加しているものと考えらえた。   Specifically, first, with regard to soybean oil and rapeseed oil, the deodorization temperature is set to a constant deodorizing time of 50 minutes using a glass device shown in FIG. The amount of trans fatty acid produced in the deodorized oil was examined by changing the temperature in the range of 180 to 250 ° C. When the deodorization temperature is plotted on the horizontal axis (x) and the amount of trans fatty acid produced is plotted on the vertical axis (y), the result shown in FIG. 2 is obtained and increases exponentially as the deodorization temperature increases. I thought it was.

そこで、このプロットが収まる近似曲線を描いた。図2中の近似曲線は、ネイピア数(e)を底とする指数関数であり、決定係数R(Rは相関係数である。)は0.9以上となった。よって、1に近い正の相関があることからみて指数関数として推定できると判断した。 Therefore, an approximate curve was drawn to fit this plot. The approximate curve in FIG. 2 is an exponential function based on the Napier number (e), and the determination coefficient R 2 (R is a correlation coefficient) is 0.9 or more. Therefore, it was judged that it can be estimated as an exponential function in view of the positive correlation close to 1.

次に、脱臭温度を230℃の一定として、脱臭時間を半分にするとトランス脂肪酸量は減少し、2倍にするとトランス脂肪酸量は増加した。また、水蒸気吹込量を2倍にするとトランス脂肪酸量は減少し、脱臭時間と水蒸気吹込量とは反比例の関係と考えられた。また、この時の増減量は概ね、脱臭温度の±5℃に相当するとみなすことができた。これらのことを総合的に表す指数関数として、下記の数1の式の左項の関係式を創出して、トランス脂肪酸の生成量が0.5%以下となる範囲を検討した結果、その範囲は3以下であるとしたのである。   Next, when the deodorization temperature was constant at 230 ° C. and the deodorization time was halved, the amount of trans fatty acid decreased, and when it was doubled, the amount of trans fatty acid increased. Moreover, when the amount of steam blown was doubled, the amount of trans fatty acid decreased, and it was considered that the deodorization time and the amount of steam blown were inversely related. Moreover, the increase / decrease amount at this time was considered to correspond to the deodorization temperature of ± 5 ° C. in general. As an exponential function that comprehensively expresses these, the following relational expression in the formula (1) is created, and the range in which the amount of trans fatty acid produced is 0.5% or less is examined. Is 3 or less.

Figure 0005955119
Figure 0005955119

Figure 0005955119
Figure 0005955119

一方、食用油の風味や色調を良くするには、できるだけ原料油の不純物を取り除く必要があるので、脱臭温度を高くすることや脱臭時間を長くすること、及び吹込水蒸気量を多くすることが有効であるが、過度にしすぎると本来含有されている抗酸化物質まで取り除かれるので適度な範囲にしておくことが必要であると考え、数2の式の左項の関係式を創出して、適切な範囲を検討した結果、その範囲は50以上300以下としたのである。   On the other hand, in order to improve the flavor and color of edible oil, it is necessary to remove impurities from the raw oil as much as possible. Therefore, it is effective to increase the deodorization temperature, lengthen the deodorization time, and increase the amount of blown water vapor. However, if it is too much, it will remove the antioxidants originally contained, so we think that it is necessary to keep it in an appropriate range. As a result of studying a range, the range is set to 50 or more and 300 or less.

すなわち、本願の発明では、脱臭工程を含む食用油脂の製造方法において、前記脱臭工程を、バッチ式またはトレイ型半連続式脱臭装置を用いて真空度10hPa以下で脱臭温度200℃以上で行ない、その際にトランス脂肪酸生成量を0.5質量%以下に抑制し、かつ脱臭工程前の原料油脂に含有されるトコフェロール類を脱臭工程後に80%以上残存させるように、前記脱臭温度、脱臭時間および前記脱臭温度での水蒸気吹込量の油に対する質量比率を特定の関係性によって調整することによる食用油脂の製造方法としたのである。   That is, in the invention of the present application, in the method for producing edible fats and oils including a deodorization step, the deodorization step is performed using a batch type or tray type semi-continuous deodorization device at a vacuum degree of 10 hPa or less and a deodorization temperature of 200 ° C. or more. The deodorizing temperature, the deodorizing time, and the above, so that the trans fatty acid production amount is suppressed to 0.5% by mass or less, and the tocopherols contained in the raw oil and fat before the deodorizing step remain 80% or more after the deodorizing step. It was set as the manufacturing method of edible oil and fat by adjusting the mass ratio with respect to the oil of the amount of water vapor | steam blowing in deodorizing temperature by specific relationship.

上記特定の関係性をもつ調整が、上記脱臭温度をT℃で示し、上記脱臭時間をM分で示し、前記脱臭温度での油の質量に対する水蒸気吹込量の比率をS質量%で示すとき、T、M、Sの変数を含む上記の数1および数2の式で示される関係を満足する調整であるようにした上記の食用油脂の製造方法とすることが好ましい。   When the adjustment having the specific relationship indicates the deodorization temperature in T ° C, the deodorization time in M minutes, and the ratio of the amount of steam blown to the mass of oil at the deodorization temperature in S mass%, It is preferable to use the above-described method for producing edible oils and fats that is adjusted to satisfy the relationship represented by the formulas 1 and 2 including the variables T, M, and S.

また、上記脱臭温度(T℃)が210〜240℃であり、脱臭時間(M分)が10〜100分であり、かつ脱臭温度での水蒸気吹込量の油に対する比率(S質量%)が、1〜10質量%である上記の食用油脂の製造方法とすることが好ましい。   Further, the deodorization temperature (T ° C.) is 210 to 240 ° C., the deodorization time (M minutes) is 10 to 100 minutes, and the ratio of water vapor blowing amount at the deodorization temperature to oil (S mass%) is It is preferable to set it as the manufacturing method of said edible oil and fat which is 1-10 mass%.

また、上記脱臭工程前の原料油脂が、トランス脂肪酸含量0.2質量%以下であり、かつ脂肪酸組成のジエン脂肪酸質量%(X)とトリエン脂肪酸質量%(Y)との関係が、下記の数3に示される関係を満足する油脂である食用油脂の製造方法とすることが好ましい。   Moreover, the raw material fats and oils before the said deodorizing process are trans fatty acid content 0.2 mass% or less, and the relationship between the diene fatty acid mass% (X) and triene fatty acid mass% (Y) of a fatty acid composition is the following number. It is preferable to set it as the manufacturing method of the edible fats and oils which are the fats and oils which satisfy the relationship shown by 3. FIG.

Figure 0005955119
Figure 0005955119

上記脱臭温度(T℃)が、215〜235℃であり、かつ数1で示される式の右辺が0.2〜2であるように調整される上記の食用油脂の製造方法とすることが、トランス脂肪酸の低減効果と脱臭後の品質のバランスがとれたものとなるので好ましい。   The deodorizing temperature (T ° C) is 215 to 235 ° C, and the production method of the edible oil and fat is adjusted so that the right side of the formula shown in Equation 1 is 0.2 to 2, This is preferable because the balance between the effect of reducing trans fatty acids and the quality after deodorization can be achieved.

さらには、上記脱臭工程前の原料油脂に、アルカリ処理及び吸着剤処理を施して酸価を0.3以下に低減させ、かつ色調を50以下に低減させる上記の食用油脂の製造方法とすることがより好ましい。   Furthermore, the raw oil and fat before the deodorizing step is subjected to alkali treatment and adsorbent treatment to reduce the acid value to 0.3 or less and to reduce the color tone to 50 or less. Is more preferable.

本願の発明によれば、食用油脂の製造方法における脱臭工程を、トランス脂肪酸生成量を所定量以下に抑制し、かつ原料油に含有されるトコフェロール類を所定量以上残存させるように脱臭温度、脱臭時間および脱臭温度での水蒸気吹込量の油に対する質量比率を調整することによって行なうので、トランス脂肪酸の生成を従来の精製油脂より大幅に低減し、かつ風味や酸化安定性に影響を及ぼす不純物を充分に除去するだけでなく、酸化安定性、風味安定性をも向上させた食用油脂を製造可能にする利点がある。   According to the invention of the present application, the deodorizing step in the method for producing edible fats and oils is performed such that the amount of trans fatty acid produced is suppressed to a predetermined amount or less, and the tocopherols contained in the raw material oil remain at a predetermined amount or more. Adjusting the mass ratio of the amount of water vapor blown at the time and deodorization temperature to the oil makes it possible to significantly reduce the production of trans fatty acids compared to conventional refined fats and to have sufficient impurities to affect flavor and oxidative stability In addition, there is an advantage that it is possible to produce an edible oil and fat with improved oxidation stability and flavor stability.

また、可及的に簡易で安価な製造工程を採用できるようになり、食用油脂製造産業における利用価値を高める利点もある。   Moreover, it becomes possible to adopt a manufacturing process that is as simple and inexpensive as possible, and there is also an advantage of increasing the utility value in the edible fat and oil manufacturing industry.

実施例に用いた脱臭装置の模式図Schematic diagram of the deodorizing device used in the examples 脱臭試験における脱臭温度とトランス脂肪酸の生成量の関係を示す図表Chart showing the relationship between the deodorization temperature and the amount of trans fatty acid produced in the deodorization test

本願発明の実施形態に用いる食用油脂の脱臭装置は、バッチ式またはトレイ型半連続式脱臭装置を使用することができ、シングルトレイや二段式の回文式脱臭装置でも使用可能であるが、効率的な製造を行なうにはガードラー型のような半連続多段型脱臭装置が好ましい。   The deodorizing apparatus for edible oils and fats used in the embodiment of the present invention can use a batch type or a tray type semi-continuous deodorizing apparatus, and can be used in a single tray or a two-stage palindromic deodorizing apparatus, For efficient production, a semi-continuous multi-stage deodorizing apparatus such as a Gardler type is preferable.

脱臭工程前の原料油脂については、動植物油脂やその水素添加油脂、分別油脂、エステル交換油脂から選ばれる1種またはこれらの混合物を使用することができる。具体的な原料油脂としては、なたね油、大豆油、コーン油、ひまわり油、米油、紅花油、綿実油、パーム油、牛脂、豚脂等を挙げることができる。または、これらの油脂を分別した分別油、混合油、または水素添加油、エステル交換反応などにより脂肪酸組成を調整したエステル交換油も原料として利用できる。なお、トランス脂肪酸含量を低減させる点から部分的な水素添加をしていないものであることが好ましい。   As the raw material fat before the deodorization step, one or a mixture selected from animal and plant fats and oils, hydrogenated fats and oils, fractionated fats and oils, and transesterified fats and oils can be used. Specific examples of raw oils and fats include rapeseed oil, soybean oil, corn oil, sunflower oil, rice oil, safflower oil, cottonseed oil, palm oil, beef tallow, and lard. Or the transesterification oil which adjusted the fatty acid composition by the fractionation oil which mixed these fats and oils, mixed oil, hydrogenated oil, transesterification, etc. can be utilized as a raw material. In addition, it is preferable that the partial hydrogenation is not performed from the point of reducing the trans fatty acid content.

また、脱臭工程前の原料油脂は、脱ガム、脱酸、脱色といった通常の精製工程を経たものがよい。酸価が0.3以下、色調が50以下であるものが好ましく、さらには酸価が0.2以下であり、色調は30以下であるものがより好ましい。トランス脂肪酸の含量は、できるだけ低いことが好ましく、例えば0.2質量%以下が好ましく、より好ましくは0.1質量%以下である。   Moreover, the raw material fats and oils before a deodorizing process should have passed through the normal refining processes, such as degumming, deoxidation, and decoloring. Those having an acid value of 0.3 or less and a color tone of 50 or less are preferred, and those having an acid value of 0.2 or less and a color tone of 30 or less are more preferred. The content of trans fatty acid is preferably as low as possible, for example, preferably 0.2% by mass or less, and more preferably 0.1% by mass or less.

特に、本願発明の効果は、脱臭時にトランス異性化が起こりやすいジエン脂肪酸やトリエン脂肪酸を含有する油脂に発揮されるので、常温で液状である、大豆油、なたね油、コーン油、綿実油、米油やパームスーパーオレインや融点の低いエステル交換油等を使用できる。   In particular, since the effect of the present invention is exerted on fats and oils containing diene fatty acids and triene fatty acids that easily undergo trans isomerization at the time of deodorization, soy oil, rapeseed oil, corn oil, cottonseed oil, rice oil, Palm super olein or transesterified oil having a low melting point can be used.

本願発明の実施に好ましい油脂は、トリエン脂肪酸が25質量%以下の油脂であり、さらに好ましいのはトリエン脂肪酸が12質量%以下でジエン脂肪酸が60質量%以下の油脂である。   The fats and oils preferred for carrying out the present invention are fats and oils having a triene fatty acid of 25% by mass or less, and more preferably fats and oils having a triene fatty acid of 12% by mass or less and a diene fatty acid of 60% by mass or less.

脱臭時の温度は200〜240℃がよく、さらには210〜240℃が好ましく、215〜235℃が最も適している。脱臭温度が高いと酸価や色調は良くなるが、トランス脂肪酸の生成量が多くなり、トコフェロール類を代表とする、天然の抗酸化物質の含有量が減少する。トランス脂肪酸の生成量は、210〜220℃を変曲点として、それ以上の温度では指数曲線的に増加する。   The temperature during deodorization is preferably 200 to 240 ° C, more preferably 210 to 240 ° C, and most preferably 215 to 235 ° C. When the deodorization temperature is high, the acid value and color tone are improved, but the production amount of trans fatty acid is increased, and the content of natural antioxidants such as tocopherols is decreased. The production amount of trans fatty acid increases exponentially at temperatures above 210 to 220 ° C.

この発明でいう水蒸気吹込量は、脱臭処理の対象となる油脂に対して、脱臭温度に到達してから吹き込む水蒸気としての水の総量であり、以下、この水の総質量の油脂の質量に対する割合(100分率)を「水蒸気吹込量対油比率」と記載している。この発明における脱臭温度での水蒸気吹込量対油比率は、1〜10質量%とすることができる。   The amount of water vapor blown in the present invention is the total amount of water as water vapor blown after reaching the deodorization temperature with respect to the oil and fat to be subjected to the deodorization treatment. Hereinafter, the ratio of the total mass of this water to the mass of the oil and fat (100 fraction) is described as “water vapor blowing amount to oil ratio”. In the present invention, the water vapor blowing amount to oil ratio at the deodorizing temperature can be 1 to 10% by mass.

脱臭工程中は、真空度を10hPa以下に維持しておく必要がある。水蒸気の吹込量を多くすると、脂肪酸をはじめとする油脂中の不純物が多く除去され、指標としての酸価が低下する。しかしながら、トコフェロール類をはじめとする油脂中の酸化防止成分も除去されやすくなるので、脱臭時間や脱臭温度とのバランスをとることが重要となる。
よって、脱臭時間は、10〜100分の間で脱臭温度と脱臭温度での水蒸気吹込量対油比率に関連させて、前記した数1、2の2つの式をいずれも満足するように調整する。
During the deodorization step, the degree of vacuum needs to be maintained at 10 hPa or less. When the amount of water vapor blown is increased, many impurities in the fat and oil including fatty acids are removed, and the acid value as an index is lowered. However, since antioxidant components in fats and oils including tocopherols are easily removed, it is important to balance the deodorization time and the deodorization temperature.
Therefore, the deodorization time is adjusted so as to satisfy both of the above-described two formulas 1 and 2 in relation to the deodorization temperature and the steam blowing amount to oil ratio at the deodorization temperature between 10 and 100 minutes. .

数1の式は、トランス脂肪酸の生成量に関するものであり、発明者らの詳細な検討によりトランス脂肪酸の生成量は指数関数的に表すことができ、第一には脱臭温度に依存することを示しており、次に脱臭時間に依存して増加することをも示している。   The expression of Equation 1 relates to the production amount of trans fatty acid, and the detailed production of the inventors can express the production amount of trans fatty acid exponentially, and firstly, it depends on the deodorization temperature. It also shows that it increases depending on the deodorization time.

また、水蒸気吹込量対油比率に関しては、トランス脂肪酸の生成を抑制する方向に働くことを示している。このことを別に言い換えると、脱臭時間を長くすることは脱臭温度を高くすることと同じであり、水蒸気吹込量対油比率を上げることは脱臭温度を下げることと同様の効果をもたらす。   Moreover, it has shown that it acts on the direction which suppresses the production | generation of trans fatty acid regarding water vapor | steam blowing amount with respect to oil ratio. In other words, increasing the deodorization time is the same as increasing the deodorization temperature, and increasing the steam blowing amount to oil ratio has the same effect as decreasing the deodorization temperature.

水蒸気吹込量対油比率を多くすると酸価や色調は良くなり、しかもトランス脂肪酸の生成量も抑えることができる。例えば、脱臭時間50分で水蒸気吹込量対油比率1質量%の時に対し、水蒸気吹込量対油比率2質量%とすると脱臭温度を5℃低下させるのと同様の効果となる。脱臭温度を215〜235℃、脱臭時間を20〜60分、脱臭温度と脱臭温度での水蒸気吹込量対油比率を2〜6%として数1の式の左項が0.2〜2となるようにバランスをとることが最も好ましい。   Increasing the steam blowing amount to oil ratio improves the acid value and color tone, and also suppresses the production of trans fatty acids. For example, when the steam blowing amount to oil ratio is 1% by mass with a deodorization time of 50 minutes, if the steam blowing amount to oil ratio is 2% by mass, the same effect as reducing the deodorizing temperature by 5 ° C. is obtained. Deodorization temperature is 215 to 235 ° C., deodorization time is 20 to 60 minutes, water vapor blowing amount at deodorization temperature and deodorization temperature is 2 to 6%, and the left side of equation 1 is 0.2 to 2. It is most preferable to achieve such a balance.

数2で示される式は、脱臭工程前の原料油脂に含有される主にトコフェロール類の天然酸化防止成分を脱臭工程後に80%以上残存させるようにする脱臭効果に関するものであり、これについても第一に脱臭温度に依存しつつ、脱臭時間と水蒸気吹込量対油比率も影響を及ぼす。
脱臭時間を長くすると、酸価の低下や色調の淡色化が進み、脱臭直後の油の品質は向上するが、トコフェロール類をはじめとする天然の酸化防止成分の除去も進行し、含有量が減少する。
The formula shown in Equation 2 relates to a deodorizing effect in which more than 80% of the natural antioxidant component of the tocopherols contained in the raw oil and fat before the deodorizing process remains after the deodorizing process. First, while depending on the deodorization temperature, the deodorization time and the steam blowing amount to oil ratio also affect.
If the deodorization time is lengthened, the acid value and the color tone become lighter and the oil quality immediately after deodorization improves, but the removal of natural antioxidant components such as tocopherols also progresses and the content decreases. To do.

また、水蒸気吹込量対油比率を上げることも同様の現象となる。
逆に、脱臭時間を短くすると、酸価の低下が少なくなって色調が悪化するので、脱臭温度での水蒸気吹込量対油比率を多くする必要がある。よって、酸価の低下と色の淡色化を満足させつつ、脱臭油の風味・酸化安定性を向上させるには数2で示される式で示すような特定の範囲とするのである。
In addition, raising the steam injection amount to oil ratio is the same phenomenon.
On the contrary, if the deodorization time is shortened, the decrease in the acid value is reduced and the color tone is deteriorated. Therefore, it is necessary to increase the water vapor blowing amount to oil ratio at the deodorization temperature. Therefore, in order to improve the flavor and oxidation stability of the deodorized oil while satisfying the decrease in the acid value and the lightening of the color, the specific range as shown by the equation shown in Formula 2 is used.

日本農林規格によれば、食用植物油脂の規格は各油脂毎に制定されており、規格の厳しいなたねサラダ油では、酸価が0.15以下であり、なたねサラダ油等では、色調がロビボンド法による133.4mmセルで黄20以下、赤2.0以下とされている。本願発明の製造方法によって得られる油脂は、この規格に合致するものである。   According to the Japanese Agricultural Standards, the standards for edible vegetable oils and fats are established for each oil and fat. The acid value of rape salad oil with strict standards is 0.15 or less. In the 133.4 mm cell, yellow 20 or less and red 2.0 or less. The fats and oils obtained by the production method of the present invention meet this standard.

従来のバッチ式脱臭では、250℃での脱臭時間は、50分〜60分程度であるが、本願の発明では、1例として220℃での脱臭時間25分で水蒸気吹込量対油比率が5質量%であった。   In the conventional batch type deodorization, the deodorization time at 250 ° C. is about 50 minutes to 60 minutes. However, in the invention of the present application, as an example, the deodorization time at 220 ° C. is 25 minutes and the ratio of the steam blowing amount to the oil ratio is 5 It was mass%.

例えば、大豆油は脱臭前の原料油ではトコフェロール類が1000〜1200ppm程度含有されているが、250℃、60分の脱臭では20%以上が失われることとなる。本願の発明によれば、トコフェロール類を80%以上残存させることが可能となる。   For example, soybean oil contains about 1000 to 1200 ppm of tocopherols in the raw material oil before deodorization, but 20% or more is lost by deodorization at 250 ° C. for 60 minutes. According to the present invention, 80% or more of tocopherols can remain.

本願発明の製造方法による油脂は、風味や酸化安定性が良好であるので、炒め油やフライ用に使用できる。また、トランス脂肪酸を低減したものの、まだ十分でなかった従来のマーガリン類をはじめとする各種加工油脂製品に使用することで、トランス脂肪酸を極限に近いところまで低減することができる。   Since the fats and oils by the manufacturing method of this invention are favorable in flavor and oxidation stability, they can be used for fried oil and frying. Moreover, although trans-fatty acid was reduced, trans-fatty acid can be reduced to the limit by using it for various processed fats and oil products including the conventional margarine which was not enough yet.

以下の実施例及び比較例にて使用した原料油および作製した油脂について、酸価は基準油脂分析試験法2.3.1−1996で測定し、色調は、基準油脂分析試験法2.2.1.1−1996、脂肪酸組成は基準油脂分析試験法暫15−2003にて行ない、トランス脂肪酸含有量は、基準油脂分析試験法暫17−2007、トコフェロール含量は、基準油脂分析試験法2.4.10−1996にて分析を行なった。尚、色調は、10R+Yの数値として表した。   About the raw material oil and the produced fats and oils used in the following examples and comparative examples, the acid value was measured by the standard fat and oil analysis test method 2.3.1-1996, and the color tone was determined by the standard fat and oil analysis test method 2.2. 1.1-1996, the fatty acid composition is determined in accordance with the standard oil analysis test method 15-2003, the trans fatty acid content is in the standard oil analysis test method 17-2007, and the tocopherol content is in the standard oil analysis test method 2.4. Analysis was performed at 10-1996. The color tone was expressed as a numerical value of 10R + Y.

[実施例1〜4]
図1に模式的に示した構造の脱臭装置を用い、脱臭前原料油脂Oとして、脱色大豆油1kgを2L容量のガラス製水蒸気蒸留フラスコ1に投入し、バッチ式脱臭を行なった。その際に水蒸気は、水蒸気発生器2で蒸留水WをヒータHで加熱して発生したものをフラスコ1の底部まで延びるガラス管3で供給し、その量は蒸留水2の減量をもって計測して脱臭時の水蒸気吹込量とした。
[Examples 1 to 4]
Using a deodorizing apparatus having a structure schematically shown in FIG. 1, 1 kg of decolorized soybean oil as raw material oil O before deodorization was charged into a 2 L glass steam distillation flask 1 for batch deodorization. At that time, the steam generated by heating the distilled water W with the heater H in the steam generator 2 is supplied through the glass tube 3 extending to the bottom of the flask 1, and the amount is measured by reducing the amount of the distilled water 2. The amount of water vapor blown at the time of deodorization was used.

フラスコ1には真空ポンプPを、氷水トラップ4を経由して接続して減圧状態とし、フラスコ1内の真空度はマノメータ5にて測定した。フラスコ1内の加熱はマントルヒータ6で行ない、脱臭温度に達するまでの加熱時間は34分であった。温度計7で測定される脱臭温度は220℃、225℃、230℃、235℃として、脱臭時間は50分とし、脱臭時の水蒸気吹込量対油比率は1%を目標に行ない、試験中の真空度は3hPaを維持した。なお、図1中の符号8はゴム管、9はコックである。   A vacuum pump P was connected to the flask 1 via an ice water trap 4 to reduce the pressure, and the degree of vacuum in the flask 1 was measured with a manometer 5. The inside of the flask 1 was heated by the mantle heater 6 and the heating time until reaching the deodorizing temperature was 34 minutes. The deodorization temperature measured by the thermometer 7 is 220 ° C., 225 ° C., 230 ° C., 235 ° C., the deodorization time is 50 minutes, and the steam blowing amount to oil ratio at the time of deodorization is targeted at 1%. The degree of vacuum was maintained at 3 hPa. In addition, the code | symbol 8 in FIG. 1 is a rubber tube, 9 is a cock.

原料の脱色油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を表1中に示すと共に、数1、2に示した式の左項の値を同表中に示した。なお、脱色大豆油の脂肪酸組成におけるジエン脂肪酸(C18−2)は57.0%、トリエン脂肪酸(C18−3)は7.3%であり、数3の式における左項の値は130であった。   The acid value, color tone, trans fatty acid content, tocopherol content, and flavor evaluation of the raw decolorized oil and the obtained deodorized oil are shown in Table 1, and the values in the left-hand side of the formulas shown in Equations 1 and 2 are shown in the same table. It was shown to. The diene fatty acid (C18-2) in the fatty acid composition of decolorized soybean oil was 57.0%, the triene fatty acid (C18-3) was 7.3%, and the value of the left term in the formula 3 was 130. It was.

表中の脱臭油の風味は、下記の基準に従って評価した。
○ 異味異臭なく良好
△ 僅かに原料特有の味がする
× 不快な味があり、食するのに不適
The flavor of the deodorized oil in the table was evaluated according to the following criteria.
○ Good with no off-flavors and odors △ Slightly peculiar to the ingredients × Unpleasant taste, unsuitable for eating

[比較例1〜4]
比較例1〜4においては、実施例1における脱臭温度を順に180℃、210℃、240℃、250℃に設定することの他、表1に示される条件で調整したこと以外は、実施例1と同様に脱臭工程を行ない、得られた食用油脂の評価を表1中に併記した。
[Comparative Examples 1 to 4]
In Comparative Examples 1 to 4, the deodorization temperature in Example 1 was set to 180 ° C., 210 ° C., 240 ° C., and 250 ° C. in addition to those in Example 1, except that it was adjusted under the conditions shown in Table 1. The deodorizing step was performed in the same manner as above, and the evaluation of the resulting edible oil / fat is also shown in Table 1.

Figure 0005955119
Figure 0005955119

表1に示す結果からも明らかなように、実施例の製法によって得られた油脂は、トランス脂肪酸の生成量が0.5%以下であり、酸価、色調共に日本農林規格以下であり、風味も良好で、トコフェロールの残存量も80%以上であった。   As is clear from the results shown in Table 1, the fats and oils obtained by the production methods of the examples have a trans fatty acid production amount of 0.5% or less, both acid value and color tone that are below the Japanese Agricultural Standards, and flavor. The residual amount of tocopherol was 80% or more.

これに対し、比較例1及び2ではトランス脂肪酸は低いが、酸価や色調が不良であり、比較例3や4ではトランス脂肪酸の生成量が多く、低減効果が不十分であった。   On the other hand, although the trans fatty acid was low in Comparative Examples 1 and 2, the acid value and color tone were poor, and in Comparative Examples 3 and 4, the amount of trans fatty acid produced was large and the reduction effect was insufficient.

[実施例5〜7]
実施例5〜7は、実施例1の製造方法で用いた脱色大豆油を脱色なたね油に変更し、脱臭温度を順に220℃、230℃、235℃に設定したこと以外は、実施例1と同様にして脱臭工程を行なった。真空度は3hPaを維持できていた。原料の脱色油および得られた脱臭油の評価として、酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価と、数1、2に示した式の左項を表2中に示した。
[Examples 5 to 7]
Examples 5 to 7 were the same as Example 1 except that the decolorized soybean oil used in the production method of Example 1 was changed to decolored rapeseed oil and the deodorization temperatures were sequentially set to 220 ° C, 230 ° C and 235 ° C. The deodorization process was performed. The degree of vacuum was maintained at 3 hPa. Table 2 shows the acid value, the color tone, the trans fatty acid content, the tocopherol content, the flavor evaluation, and the left side of the formulas shown in Equations 1 and 2 as the evaluation of the raw material decolorized oil and the obtained deodorized oil.

なお、脱色なたね油の脂肪酸組成におけるジエン脂肪酸(C18−2)は20.3%、トリエン脂肪酸(C18−3)は10.3%であったので、数3の式における左項は123.3であった。   Since the diene fatty acid (C18-2) in the fatty acid composition of bleached rapeseed oil was 20.3% and the triene fatty acid (C18-3) was 10.3%, the left term in the formula 3 was 123.3. there were.

[比較例5〜7]
実施例1における脱臭温度を180℃、240℃、250℃に設定することの他、表2
に示される条件で調整したこと以外は、実施例1と同様に脱臭を行ない、得られた油脂の評価を表2中に併記した。
[Comparative Examples 5 to 7]
In addition to setting the deodorization temperature in Example 1 to 180 ° C, 240 ° C, 250 ° C, Table 2
Deodorization was carried out in the same manner as in Example 1 except that the conditions were adjusted under the conditions shown in Table 1, and the evaluation of the resulting fats and oils was also shown in Table 2.

Figure 0005955119
Figure 0005955119

表2に示す結果からも明らかなように、脱色なたね油から実施例の製造方法で得られた油脂は、トランス脂肪酸生成量が0.5%以下であり、酸価、色調共に日本農林規格以下であり、風味も良好で、トコフェロールの残存量も80%以上であった。   As is clear from the results shown in Table 2, the fats and oils obtained from the decolored rapeseed oil by the production methods of the examples have a trans fatty acid production amount of 0.5% or less, and both the acid value and color tone are below the Japanese Agricultural Standard. And the flavor was good, and the residual amount of tocopherol was 80% or more.

これに対し、比較例5ではトランス脂肪酸は低いが、酸価や色調が不良であり、比較例6や7ではトランス脂肪酸の生成量が多く、低減効果が不十分であった。   On the other hand, although the trans fatty acid was low in Comparative Example 5, the acid value and the color tone were poor. In Comparative Examples 6 and 7, the amount of trans fatty acid produced was large, and the reduction effect was insufficient.

[実施例8〜10]
実施例1の製造方法で用いた脱色大豆油における脱臭温度と脱臭時の水蒸気吹込量対油比率を表3に示すようにしたこと以外は、実施例1と同様にして脱臭を行なった。
[Examples 8 to 10]
Deodorization was carried out in the same manner as in Example 1 except that the deodorizing temperature in the decolorized soybean oil used in the production method of Example 1 and the ratio of the steam blowing amount to the oil ratio during deodorization were as shown in Table 3.

原料の脱色油および得られた脱臭油の評価として、酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を示すと共に、数1、2に示した式の左項の値を表3中に示した。   As an evaluation of the raw material decolorized oil and the obtained deodorized oil, the acid value, color tone, trans fatty acid content, tocopherol content, flavor evaluation are shown, and the values in the left-hand side of the formulas shown in Equations 1 and 2 are shown in Table 3. Indicated.

Figure 0005955119
Figure 0005955119

表3に示す結果から明らかなように、脱臭温度が低い場合でも脱臭時間と水蒸気吹込量対油比率を増やすことで、実施例8〜10の製造方法で得られた油脂は、トランス脂肪酸の生成量を低く抑えながらも酸価、色調、風味も良好であり、トコフェロールの残存量も80%以上であった。   As is apparent from the results shown in Table 3, the fats and oils obtained by the production methods of Examples 8 to 10 were produced by increasing the deodorization time and the steam blowing amount to the oil ratio even when the deodorization temperature was low, thereby producing trans fatty acids. Although the amount was kept low, the acid value, color tone, and flavor were good, and the residual amount of tocopherol was 80% or more.

[実施例11〜14]
実施例5の製造方法で用いた脱色なたね油を原料とし、脱臭温度220℃または230℃で脱臭時間を35分とし、5hPa以下の真空度を維持して脱臭時の水蒸気吹込量対油比率を1.5%と2.5%とする条件で脱臭を行なった。
原料の脱色油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価と、数1、2、3に示した式の左項の値を表4中に併記した。
[Examples 11 to 14]
The decolorized rapeseed oil used in the production method of Example 5 is used as a raw material, the deodorization temperature is 220 ° C. or 230 ° C., the deodorization time is 35 minutes, the vacuum degree of 5 hPa or less is maintained, and the water vapor blowing amount to oil ratio during deodorization is 1. Deodorization was performed under conditions of 5% and 2.5%.
In Table 4, the acid value, color tone, trans fatty acid content, tocopherol content, flavor evaluation of the raw material decolorized oil and the obtained deodorized oil, and the values in the left-hand side of the formulas shown in Formulas 1, 2, and 3 are shown.

Figure 0005955119
Figure 0005955119

表4の結果から明らかなように、水蒸気吹込量対油比率を増やすことで、実施例の製造方法による油脂は、酸価をさらに低減できるだけでなく、トランス脂肪酸の生成量も低く抑えられた油脂となっていた。   As is apparent from the results in Table 4, by increasing the steam injection amount to the oil ratio, the fats and oils produced by the production methods of the examples not only can further reduce the acid value, but also reduce the amount of trans fatty acids produced. It was.

[実施例15〜21、比較例8]
実施例1の製造方法において、原料の脱色大豆油を5hPa以下の真空度を維持して脱臭温度、脱臭時間、脱臭時の水蒸気吹込量対油比率を表5に示すように変動させたこと以外は、実施例1と同様にして脱臭を行なった。
[Examples 15 to 21, Comparative Example 8]
In the production method of Example 1, the raw material decolorized soybean oil was maintained at a vacuum level of 5 hPa or less, and the deodorization temperature, the deodorization time, and the water vapor blowing amount to the oil ratio during deodorization were varied as shown in Table 5. Was deodorized in the same manner as in Example 1.

脱色大豆油は、トコフェロール含量が保管中に若干減少していたが、そのまま使用した。原料の脱色油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を示すと共に、数1、2、3に示した式の左項の値を表5中に併記した。   The decolorized soybean oil was used as it was, although the tocopherol content was slightly reduced during storage. It shows the acid value, color tone, trans fatty acid content, tocopherol content, and flavor evaluation of the raw decolorized oil and the obtained deodorized oil, and the values in the left-hand side of the formulas shown in Formulas 1, 2, and 3 are also shown in Table 5. did.

Figure 0005955119
Figure 0005955119

表5に示す結果から明らかなように、脱臭温度、脱臭時間、脱臭時の水蒸気吹込量対油比率を実施例の製造方法でバランスよく調整した実施例15〜21の油脂は、トランス脂肪酸の生成量が0.5%以下であり、酸価、色調、風味も良好で、トコフェロールの残存量も80%以上であった。   As is apparent from the results shown in Table 5, the fats and oils of Examples 15 to 21 in which the deodorization temperature, the deodorization time, and the water vapor blowing amount at the time of deodorization to the oil ratio were adjusted in a well-balanced manner by the production method of the Examples The amount was 0.5% or less, the acid value, the color tone and the flavor were good, and the residual amount of tocopherol was 80% or more.

これに対し、比較例8の油脂では、数2の式を満足しないS,M,Tの値を採用したので、トコフェロールの残存量が80%未満であった。
On the other hand, in the fats and oils of Comparative Example 8, since the values of S, M, and T that do not satisfy the formula 2 were adopted, the residual amount of tocopherol was less than 80%.

[実施例22]
実施例15の製造方法において、脱色大豆油の脱臭温度を220℃、脱臭時間40分、脱臭時の水蒸気吹込量対油比率8.0%とし、真空度8hPaとしたこと以外は同様にして脱臭工程を行なった。原料の脱色大豆油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を示すと共に、数1、2、3に示した式の左項の値を表6中に併記した。
[Example 22]
In the production method of Example 15, the deodorizing temperature of the decolorized soybean oil was 220 ° C., the deodorizing time was 40 minutes, the steam blowing amount at the time of deodorizing was 8.0%, and the degree of vacuum was 8 hPa. The process was performed. Table 6 shows the acid value, color tone, trans fatty acid content, tocopherol content, and flavor evaluation of the raw material decolorized soybean oil and the obtained deodorized oil. Also written.

Figure 0005955119
Figure 0005955119

表6の結果からも明らかなように、実施例22の大豆油はトランス脂肪酸の生成量は相当に低く、脱臭油の品質は優れたものであった。   As is apparent from the results in Table 6, the soybean oil of Example 22 produced a considerably low amount of trans fatty acid, and the quality of the deodorized oil was excellent.

[実施例23、比較例9]
実施例1において、脱色大豆油の代わりに脱色豚脂400gを用い、1L容量のガラス製水蒸気蒸留フラスコを用いて真空度2hPaで脱臭を行なったこと、脱臭時の水蒸気吹込量対油比率を表7に示した通りとしたこと以外は実施例1と同様にして脱臭工程を行ない、食用油脂を製造した。
[Example 23, comparative example 9]
In Example 1, 400 g of decolorized pork fat was used in place of decolored soybean oil, and deodorization was performed at a vacuum degree of 2 hPa using a 1 L glass steam distillation flask, and the ratio of the amount of steam blown to oil during deodorization was shown. A deodorizing step was carried out in the same manner as in Example 1 except that it was as shown in FIG.

原料の脱色豚脂および得られた食用油脂の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を表7中に示すと共に、数1〜3に示した式の左項の値を同表中に併記した。なお、脱色豚脂の脂肪酸組成におけるジエン脂肪酸(C18−2)は7.9%、トリエン脂肪酸(C18−3)は0.7%であったので、数3の式の左項は14.9であった。   Table 7 shows the acid value, color tone, trans fatty acid content, tocopherol content, and flavor evaluation of the raw material decolorized pork fat and the obtained edible oil and fat, and the values in the left-hand side of the formulas shown in Equations 1 to 3 are shown in the same table. It was written together. The diene fatty acid (C18-2) in the fatty acid composition of decolorized pork fat was 7.9%, and the triene fatty acid (C18-3) was 0.7%. Met.

Figure 0005955119
Figure 0005955119

表7の結果からも明らかなように、動物脂である豚脂に対しても実施例22は比較例9に比べてトランス脂肪酸の生成量は、実質的に全く生成しない程度に低く、脱臭油の品質は優れたものであった。   As is clear from the results in Table 7, the amount of trans fatty acid produced in Example 22 was lower than that in Comparative Example 9 for pork fat, which is animal fat. The quality was excellent.

[実施例24、比較例10]
実施例1において、原料の脱色大豆油の代わりに脱色大豆油320gと脱色えごま油80gを混合した大豆えごま混合油400gを用いたこと、1L容量のガラス製水蒸気蒸留フラスコを用いて真空度2hPaで脱臭を行なったこと、表8に示した脱臭時の水蒸気吹込量対油比率としたこと以外は実施例1と同様にして脱臭工程を行ない、食用油脂を製造した。
[Example 24, Comparative Example 10]
In Example 1, 400 g of soybean sesame mixed oil obtained by mixing 320 g of decolorized soybean oil and 80 g of decolorized sesame oil was used in place of the raw material decolorized soybean oil, and the degree of vacuum was 2 hPa using a 1 L glass steam distillation flask. A deodorizing step was performed in the same manner as in Example 1 except that deodorization was performed and that the water vapor blowing amount at the time of deodorization and the oil ratio shown in Table 8 were used to produce edible fats and oils.

原料に用いた脱色大豆えごま混合油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を示すと共に、数1、2、3に示した式の左項の値を表8中に併記した。なお、大豆えごま混合油の脂肪酸組成におけるジエン脂肪酸(C18−2)は45.8%、トリエン脂肪酸(C18−3)は17.2%であり、数3の式に示される左項は217.8であった。   The acid value, color tone, trans fatty acid content, tocopherol content, and flavor evaluation of the decolorized soybean sesame mixed oil and the obtained deodorized oil used as raw materials are shown. This is also shown in Table 8. The diene fatty acid (C18-2) in the fatty acid composition of soybean sesame mixed oil is 45.8%, the triene fatty acid (C18-3) is 17.2%, and the left term shown in the formula 3 is 217. It was 8.

Figure 0005955119
Figure 0005955119

表8の結果からも明らかなように、脱臭工程前の原料油脂が、ジエン脂肪酸とトリエン脂肪酸の含量の高い混合油を使用した実施例24は、トランス脂肪酸の生成量が相当に低くなり、脱臭油の品質は優れたものであった。   As is apparent from the results in Table 8, in Example 24 in which the raw oil / fat before the deodorization process uses a mixed oil having a high content of diene fatty acid and triene fatty acid, the production amount of trans fatty acid is considerably low, The quality of the oil was excellent.

一方、数1、2の条件を満足しない脱臭工程条件を採用した比較例10はトランス脂肪酸の生成量は多く、トコフェロールの残存量は相当に低いものであった。   On the other hand, Comparative Example 10 employing the deodorization process conditions that do not satisfy the conditions of Equations 1 and 2 produced a large amount of trans fatty acid, and the residual amount of tocopherol was considerably low.

[実施例25]
脱色なたね油900gとパーム極度硬化油100gを混合し、70℃まで加温した後、油脂に対し3gのナトリウムメトキシドを加え、30分間攪拌混合してランダムエステル交換反応を行なった。反応後、水洗して触媒を除去し、得られた反応油に活性白土を1%添加して105℃減圧下で30分間吸着処理をした後、濾紙にてろ過し、エステル交換油800gを得た。
[Example 25]
After mixing 900 g of decolored rapeseed oil and 100 g of palm extremely hardened oil and heating to 70 ° C., 3 g of sodium methoxide was added to the oil and fat, and the mixture was stirred and mixed for 30 minutes to carry out a random transesterification reaction. After the reaction, the catalyst is removed by washing with water, and 1% of activated clay is added to the obtained reaction oil, followed by adsorption treatment at 105 ° C. under reduced pressure for 30 minutes, followed by filtration with filter paper to obtain 800 g of transesterified oil. It was.

得られたエステル交換油400gについて、1L容量のガラス製水蒸気蒸留フラスコを用いて真空度2hPaで脱臭を行なった。脱臭温度、脱臭時間、脱臭時の水蒸気吹込量対油比率は表9に示したとおりであり、原料の脱色油および得られた脱臭油の酸価、色調、トランス脂肪酸含量、トコフェロール含量、風味評価を示すと共に、数1、2、3に示した式の左項の値を表9中に併記した。   About 400 g of the obtained transesterified oil, deodorization was performed at a degree of vacuum of 2 hPa using a 1 L glass steam distillation flask. The deodorization temperature, deodorization time, and steam injection amount to oil ratio at the time of deodorization are as shown in Table 9. The acid value, color, trans fatty acid content, tocopherol content, and flavor evaluation of the raw decolorized oil and the obtained deodorized oil In Table 9, the values of the left term of the formulas shown in equations 1, 2, and 3 are also shown.

なお、エステル交換油の脂肪酸組成におけるジエン脂肪酸(C18−2)は17.0%、トリエン脂肪酸(C18−3)は8.7%であったので、数3の式に示す左項は、104であった。   Since the diene fatty acid (C18-2) in the fatty acid composition of the transesterified oil was 17.0% and the triene fatty acid (C18-3) was 8.7%, the left term shown in the formula 3 is 104 Met.

Figure 0005955119
Figure 0005955119

表9の結果からも明らかなように、エステル交換油に対しても実施例25は、トランス脂肪酸の生成量は相当に低く、しかも脱臭油の品質は優れたものであった。   As is clear from the results in Table 9, even in the case of transesterified oil, the amount of trans fatty acid produced in Example 25 was considerably low, and the quality of the deodorized oil was excellent.

[実施例26〜27]
ガードラー式トレイ型半連続式脱臭装置を用いて、真空度4hPaでコーン油、大豆油の脱臭を実施した。
トレイ数は5であり、トレイの油脂仕込量は1250kgとした。脱臭温度は220℃とし、第1トレイと第2トレイで220℃まで加熱し、第3トレイと第4トレイで脱臭を行なった。
[Examples 26 to 27]
Corn oil and soybean oil were deodorized at a vacuum degree of 4 hPa using a Gardler tray type semi-continuous deodorization apparatus.
The number of trays was 5, and the amount of fat and oil charged in the tray was 1250 kg. The deodorization temperature was 220 ° C., the first tray and the second tray were heated to 220 ° C., and the third tray and the fourth tray were deodorized.

コーン油の場合は、各トレイで24分ずつ、計48分の保持時間(脱臭時間)とし、脱臭時の水蒸気吹込量対油比率を1.1%とした。   In the case of corn oil, the holding time (deodorizing time) was 48 minutes for each tray for 24 minutes, and the water vapor blowing amount to oil ratio during deodorization was 1.1%.

大豆油の場合は各トレイで20分ずつ、計40分の保持時間(脱臭時間)とし、脱臭時の水蒸気吹込量対油比率を1.9%とした。   In the case of soybean oil, the retention time (deodorization time) was 20 minutes in each tray for a total of 40 minutes, and the steam blowing amount to oil ratio during deodorization was 1.9%.

第5トレイでの冷却を経た後、完全に窒素気流下となっているタンクに移送した脱臭油脂をサンプリングして品質を調べた。この結果を表10に示した。尚、脱臭前の原料油についても表10に併記した。   After cooling in the fifth tray, the quality of the deodorized oil / fat transferred to a tank completely under a nitrogen stream was sampled to examine the quality. The results are shown in Table 10. The raw oil before deodorization is also shown in Table 10.

また、得られた脱臭油について、保存の風味評価試験とその評価を以下のように行ない、その結果を表10中に併記した。   Moreover, about the obtained deodorized oil, the preservation | save flavor evaluation test and its evaluation were done as follows, and the result was written together in Table 10.

<保存後の風味評価試験>
脱臭油を500ml容スチール缶に500g入れ、密栓後20℃に90日間保存した後、下記の基準に従い風味評価及び過酸化物価を行なった。
○: ほとんど無味か、微かに戻り臭がある程度であり良好である
△: 戻り臭や少し劣化した味が感じられる
×: 劣化しており、食用に不適である
<Flavor evaluation test after storage>
500 g of deodorized oil was put into a 500 ml steel can, and after sealing and stored at 20 ° C. for 90 days, flavor evaluation and peroxide value were performed according to the following criteria.
○: Almost tasteless or slightly return odor to some extent and good △: Return odor and slightly degraded taste are felt ×: Deteriorated and unfit for consumption

[比較例11〜12]
実施例26と27において、脱臭温度を250℃、脱臭時間を48分とし、脱臭時の水蒸気吹込量対油比率を通常の1.1%としたこと以外は同様に行ない、結果を表10中に併記した。
[Comparative Examples 11-12]
In Examples 26 and 27, the same procedure was performed except that the deodorization temperature was 250 ° C., the deodorization time was 48 minutes, and the water vapor blowing amount to oil ratio at the time of deodorization was 1.1%, and the results are shown in Table 10. It was written together.

Figure 0005955119
Figure 0005955119

表10の結果から明らかなように、脱臭工程における脱臭温度、脱臭時間、脱臭時の水蒸気吹込量対油比率を数1、2に示す所定の関係性をもってバランスよく調整した実施例26、27の油脂は、トランス脂肪酸の生成量が0.2%以下であり、酸価、色調、風味も良好で、トコフェロールの残存量も80%以上であった。   As is clear from the results of Table 10, the deodorization temperature, the deodorization time, and the water vapor blowing amount at the time of deodorization in the deodorization step were adjusted in a well-balanced manner with the predetermined relationship shown in Equations 1 and 2 in Examples 26 and 27. The fat and oil had a trans fatty acid production of 0.2% or less, an acid value, a color tone and a good flavor, and a residual amount of tocopherol of 80% or more.

これに対し、比較例11、12の脱臭工程で製造された油脂では、数1、2に示す所定の関係性を満足せずに、トコフェロールの残存量が80%未満であり、トランス脂肪酸の生成量が0.5質量%を超えていた。   On the other hand, in the fats and oils produced in the deodorization process of Comparative Examples 11 and 12, the remaining amount of tocopherol is less than 80% without satisfying the predetermined relationship shown in Equations 1 and 2, and the production of trans fatty acid The amount exceeded 0.5% by mass.

[実施例28]
実施例27において、大豆油に代えて脱色なたね油を原料として脱臭を行なった。脱色なたね油は、色調が80であったので、再度の脱色処理を行なった。その場合、なたね油20トンに対して活性白土を0.5%添加して90℃減圧下で30分間吸着処理をした後、フィルタープレスにてろ過し、得られたなたね脱色油を脱臭装置に供した。得られた脱色なたね油の酸価は、0.11であり、色調は19であった。
[Example 28]
In Example 27, deodorization was performed using decolored rapeseed oil instead of soybean oil as a raw material. The decolored rapeseed oil had a color tone of 80, so the decolorization process was performed again. In that case, 0.5% of activated clay was added to 20 tons of rapeseed oil, adsorbed for 30 minutes under reduced pressure at 90 ° C., filtered through a filter press, and the rapeseed decolorized oil obtained was put into a deodorizing device. Provided. The acid value of the obtained decolored rapeseed oil was 0.11 and the color tone was 19.

脱臭工程は、真空度4hPaで脱色油脂を220℃、40分間脱臭し、脱臭なたね油を得た。脱臭なたね油及び脱臭前の脱色なたね油の品質を表11中に示した。
また、得られた脱臭油について、実施例27と同様に保存テストを行ない、その結果を表11中に併記した。
In the deodorization step, the decolorized oil was deodorized at 220 ° C. for 40 minutes at a vacuum degree of 4 hPa to obtain a deodorized rapeseed oil. Table 11 shows the quality of deodorized rapeseed oil and decolorized rapeseed oil before deodorization.
The obtained deodorized oil was subjected to a storage test in the same manner as in Example 27, and the results are also shown in Table 11.

Figure 0005955119
Figure 0005955119

表11の結果から明らかなように、脱臭工程における脱臭温度、脱臭時間、脱臭時の水蒸気吹込量対油比率を数1、2に示す所定の関係性をもってバランスよく調整した実施例28の製造方法で得られた油脂は、トランス脂肪酸の生成量が0.16と低く、酸価、色調、風味も良好で、トコフェロールの残存量も80%以上であった。特に、脱臭前の原料油に吸着剤処理を施し、色調を19に低減させたことにより、比較例7に示された油脂の色調以上に淡色のものとなった。   As is apparent from the results in Table 11, the production method of Example 28 in which the deodorization temperature, the deodorization time, and the water vapor blowing amount to the oil ratio at the time of deodorization in the deodorization step were adjusted in a well-balanced manner with the predetermined relationship shown in Equations 1 and 2. The fats and oils obtained in Example 1 had a low production amount of trans fatty acid of 0.16, good acid value, color tone and flavor, and the residual amount of tocopherol was 80% or more. In particular, the raw material oil before deodorization was treated with an adsorbent, and the color tone was reduced to 19. As a result, it became lighter than the oil color tone shown in Comparative Example 7.

1 フラスコ
2 水蒸気発生器
3 ガラス管
4 氷水トラップ
5 マノメータ
6 マントルヒータ
7 温度計
8 ゴム管
9 コック
W 蒸留水
O 原料油脂
1 Flask 2 Steam generator 3 Glass tube 4 Ice water trap 5 Manometer 6 Mantle heater 7 Thermometer 8 Rubber tube 9 Cock W Distilled water O Raw oil

Claims (6)

脱臭工程を含む食用油脂の製造方法において、前記脱臭工程を、バッチ式またはトレイ型半連続式脱臭装置を用いて真空度10hPa以下で脱臭温度200℃以上で行ない、その際にトランス脂肪酸生成量を0.5質量%以下に抑制し、かつ脱臭工程前の原料油脂に含有されるトコフェロール類を脱臭工程後に80%以上残存させるように、前記脱臭温度、脱臭時間および前記脱臭温度での水蒸気吹込量の油に対する質量比率を調整し、この調整が、上記脱臭温度をT℃で示し、上記脱臭時間をM分で示し、前記脱臭温度での水蒸気吹込量の油に対する質量比率をS質量%で示すとき、T、M、Sの変数を含む下記の数1および数2の式を用いて行なう調整であることを特徴とする食用油脂の製造方法。
Figure 0005955119
Figure 0005955119
In the method for producing edible fats and oils including a deodorization step, the deodorization step is performed using a batch type or tray type semi-continuous deodorization device at a vacuum degree of 10 hPa or less and a deodorization temperature of 200 ° C. or more. The amount of steam blown at the deodorization temperature, the deodorization time, and the deodorization temperature so that the tocopherols contained in the raw oil and fat before the deodorization step remain at 80% or more after being suppressed to 0.5% by mass or less. Adjusting the mass ratio of oil to oil, this adjustment shows the deodorization temperature in T ° C., the deodorization time in M minutes, and the mass ratio of water vapor blown in the deodorization temperature to oil in S mass%. A method for producing edible fats and oils, characterized in that the adjustment is performed using the following formulas 1 and 2 including variables of T, M, and S.
Figure 0005955119
Figure 0005955119
上記脱臭温度(T℃)が210〜240℃であり、脱臭時間(M分)が10〜100分であり、かつ脱臭温度での水蒸気吹込量の油に対する比率(S質量%)が、1〜10質量%である請求項1に記載の食用油脂の製造方法。   The deodorizing temperature (T ° C.) is 210 to 240 ° C., the deodorizing time (M minutes) is 10 to 100 minutes, and the ratio (S mass%) of the water vapor blowing amount at the deodorizing temperature to the oil is 1 to It is 10 mass%, The manufacturing method of the edible fat according to claim 1. 上記脱臭工程前の原料油脂が、トランス脂肪酸含量0.2質量%以下であり、かつ脂肪酸組成のジエン脂肪酸質量%(X)とトリエン脂肪酸質量%(Y)との関係が、下記の数3に示される関係を満足する油脂である請求項1または2に記載の食用油脂の製造方法。
Figure 0005955119
The raw oil and fat before the deodorizing step has a trans fatty acid content of 0.2% by mass or less, and the relationship between the diene fatty acid mass% (X) and the triene fatty acid mass% (Y) of the fatty acid composition is expressed by the following formula 3. The method for producing an edible oil or fat according to claim 1 or 2, wherein the oil or fat satisfies the relationship indicated.
Figure 0005955119
上記脱臭温度(T℃)が、215〜235℃であり、かつ数1で示される式の右辺が0.2〜2であるように調整される請求項1〜3のいずれかに記載の食用油脂の製造方法。   The said deodorizing temperature (T degreeC) is 215-235 degreeC, and the edible in any one of Claims 1-3 adjusted so that the right side of the formula shown by Formula 1 may be 0.2-2. The manufacturing method of fats and oils. 食用油脂が、大豆油、なたね油、コーン油、コメ油、綿実油、ヒマワリ油およびサフラワー油からなる群から選ばれる1種以上の食用油脂である請求項1〜4のいずれかに記載の食用油脂の製造方法。   The edible fat / oil is at least one edible fat / oil selected from the group consisting of soybean oil, rapeseed oil, corn oil, rice oil, cottonseed oil, sunflower oil and safflower oil. Manufacturing method. 上記脱臭工程前の原料油脂に、アルカリ処理及び吸着剤処理を施して酸価を0.3以下に低減させ、かつ色調を50以下に低減させる請求項1〜5のいずれかに記載の食用油脂の製造方法。   The edible oil / fat according to claim 1, wherein the raw oil / fat before the deodorization step is subjected to alkali treatment and adsorbent treatment to reduce the acid value to 0.3 or less and to reduce the color tone to 50 or less. Manufacturing method.
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