JPH0577000B2 - - Google Patents

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Publication number
JPH0577000B2
JPH0577000B2 JP61047455A JP4745586A JPH0577000B2 JP H0577000 B2 JPH0577000 B2 JP H0577000B2 JP 61047455 A JP61047455 A JP 61047455A JP 4745586 A JP4745586 A JP 4745586A JP H0577000 B2 JPH0577000 B2 JP H0577000B2
Authority
JP
Japan
Prior art keywords
oil
oils
hydrogenated
fats
weight
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP61047455A
Other languages
Japanese (ja)
Other versions
JPS62207399A (en
Inventor
Shigeru Shoji
Koken Maeda
Masato Tsukamoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tsukishima Foods Industry Co Ltd
Original Assignee
Tsukishima Foods Industry Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tsukishima Foods Industry Co Ltd filed Critical Tsukishima Foods Industry Co Ltd
Priority to JP4745586A priority Critical patent/JPS62207399A/en
Publication of JPS62207399A publication Critical patent/JPS62207399A/en
Publication of JPH0577000B2 publication Critical patent/JPH0577000B2/ja
Granted legal-status Critical Current

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  • Edible Oils And Fats (AREA)
  • Fats And Perfumes (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

[産業上の利用分野] 本発明は可塑性油脂の製造方法に関し、特にス
プレツド性(伸展性)が要求されるマーガリン、
シヨートニング及び食用加工油脂等に使用して好
適な可塑性油脂の製造方法に関するものである。 [従来の技術] 一般にマーガリン、シヨートニング等に対して
は、それらの食用時及び調理時等に安定したスプ
レツド性が要求されるのが普通であるが、かかる
スプレツド性が要求される油脂は、通常例えばサ
フラワー油、大豆油、ナタネ油及びそれらの硬化
油等を適度な稠度(可塑性)をもつように配合し
て製造されている。 [発明が解決しようとする問題点] しかしかかる油脂に関して、上記可塑性が適度
に保たれる温度域が比較的狭いことが指摘されて
居り、そして比較的一定した保型性が充分でない
等の問題があつた。ここに保型性とは換言すれば
耐熱性と同類と考えられ、又スプレツド性が要求
される製品は、具体的にパイ、ペストリー用、家
庭用マーガリン等であり、いずれもこれらが使用
される温度範囲で適切な可塑性等諸特性を具備し
ていることが強く望まれている。 [問題点を解決するための手段] 本発明者等は上記油脂特性中、特に使用温度巾
が広くすなわち温度変化に対して耐熱性があり、
そして安定したスプレツド性のある特にパイ、ペ
ストリー用及び家庭用食卓マーガリンに要求され
る可塑性油脂に関し鋭意検討を重ねた結果、特定
の油脂の選択及び組合せ、更にこれら油脂混合物
のダイレクテド(指向性)エステル交換によりそ
の最終融点を35〜45℃にすることが有効であるこ
とを見出し本発明を完成するに至つたのである。 即ち本発明は、サフラワ油、ヒマワリ油、大豆
油、コーン油、ナタネ油、綿実油、米油、落花生
油、オリーブ油から選択された1種又は2種以上
の液状植物油60〜90重量%及びパーム油、パーム
硬化油、綿実硬化油、米硬化油、カポツク硬化油
から選択された1種又は2種以上のパルミチン酸
の炭素原子の鎖長を15%以上有する油脂10〜40重
量%の混合物を、15〜25℃でダイレクテドエステ
ル交換し最終融点を35〜45℃に保持した油脂を得
る可塑性油脂の製造方法である。 上記の混合比、即ち上記液状植物油60〜90重量
%及びパルミチン酸の炭素原子の鎖長を15%以上
有する油脂10〜40重量%の範囲の下限未満あるい
はその上限を越える場合には、いづれもこの発明
の目的とするような油脂が得られない。 この混合油脂は15〜25℃でダイレクテドエステ
ル交換し、その最終融点が35〜45℃になるように
行われるが、具体的には該ダイレクテドエステル
交換反応を調整することによつて達成し得る。 本発明において上記ダイレクテドエステル交換
反応は、通常20時間程度を要するが15〜20時間で
十分である。反応温度が上記の温度範囲外では上
記反応が適切に行われず好ましくない。 上述のパルミチン酸の炭素原子の鎖長を15%以
上有する油脂中、特にパーム油に関しては、パー
ム油そのもの、またはその部分硬化油、極度硬化
油、分別油及び分別硬化油又はそれらの組合せで
選択しても良い。 各種油脂のパルミチン酸含量(%)を示すと以
下の通りである。 ナタネ油 3〜4 大豆油 9〜11 サフラワ油 6〜8 パーム極度硬化油 40〜45 パーム硬化油 40〜45 パーム油 40〜45 大豆硬化油 9〜11 綿実硬化油 21〜25 パーム核硬化油 8〜12 サフラワ硬化油 6〜8 米硬化油 15〜20 カポツク硬化油 20〜25 次に本発明において上記ダイレクテドエステル
交換は該交換反応に際して指向性をもたせて行う
反応であり、一般的には低温域で行われるのが、
慣例である。この点ランダムエステル交換(無作
為反応)と対比されるものであり、即ち一般に
は、60〜120℃の温度で10〜60分間の反応である。
これに対して本発明は、15〜25℃の温度区域で反
応に指向性を与えて行われる。そして最終油脂の
融点が35〜45℃に調整される点に特長を有する。 [作用] 本発明は上記の説明及び実施例で明らかなよう
に適切な油脂の選択及び配合組成、更にこれらの
ダイレクテドエステル交換反応により、上記要求
される油脂特性即ち可塑性等を具備した油脂が得
られる。 [実施例] 以下実施例によりこの発明を具体的に説明す
る。 実施例 1 ナタネ油800gとパーム硬化油(MP52℃)200
gを混合し100〜120℃で1時間減圧下で脱水を行
なつたのち触媒ナトリウムメチラート0.3%(対
油)加えて撹拌混合し冷却して20℃の温度を保持
して20時間ダイレクテドエステル交換を行ない、
反応終了後、当量より過剰の水で触媒を失活さ
せ、該失活を十分に行なつた後、90〜100℃まで
加温し2重量%活性白土を使用して常法通り脱色
を行ない、更に240℃1時間吹込み蒸気4.0(%)
で脱臭を行ない融点40℃のエステル交換油を得
た。 得られたエステル交換油824gに、水160g、食
塩12g、大豆レシチン2g、グリセリンモノグリ
セライド2g及び色素少量を加えて混和し、乳化
後、小型マーガリン製造機でスプレツド用マーガ
リンを製造した。 実施例 2〜5 実施例2は上記ダイレクテドエステル交換反応
を15℃で行ない、又実施例3〜5は油脂の種類及
び配合を次表の如くした外は実施例(1)と同様に行
ないダイレクテドエステル交換油を得、それらの
融点を同表に示し、更にそれぞれ実施例1と同様
にしてスプレツド用マーガリンを得た。得られた
マーガリンの特性を評価し結果を同表に示した。 比較例 1〜6 各比較例の配合は次のとおりであるが、特に比
較例2は実施例4の油脂配合で33℃に達したとき
に反応を停止させ、又比較例5、6は従来の油脂
配合で製造したものでダイレクテドエステル交換
は行つていない外は実施例1と全く同様に行つ
た。
[Industrial Application Field] The present invention relates to a method for producing plastic fats and oils, and in particular margarine, which requires spreadability (extensibility).
The present invention relates to a method for producing plastic fats and oils suitable for use in skimming, edible processing fats, and the like. [Prior Art] Generally speaking, margarine, shortening, etc. are required to have stable spreadability during eating and cooking, but oils and fats that require such spreadability are usually For example, it is manufactured by blending safflower oil, soybean oil, rapeseed oil, and their hydrogenated oils to have an appropriate consistency (plasticity). [Problems to be Solved by the Invention] However, it has been pointed out that the temperature range in which the above-mentioned plasticity is maintained appropriately is relatively narrow for such oils and fats, and there are problems such as insufficient relatively constant shape retention. It was hot. In other words, shape retention is considered to be similar to heat resistance, and products that require spreadability include pies, pastries, household margarine, etc., and these are used in all of them. It is strongly desired that the material has various properties such as appropriate plasticity over a temperature range. [Means for Solving the Problems] The present inventors have found that among the above-mentioned oil and fat properties, in particular, it has a wide operating temperature range, that is, it is heat resistant to temperature changes,
As a result of extensive research into the plastic fats and oils required for stable spreadability, especially for pies, pastries, and table margarine for home use, we have determined the selection and combination of specific fats and oils, and the direct esters of these fat mixtures. They discovered that it is effective to raise the final melting point to 35 to 45°C by exchange, leading to the completion of the present invention. That is, the present invention provides 60 to 90% by weight of one or more liquid vegetable oils selected from safflower oil, sunflower oil, soybean oil, corn oil, rapeseed oil, cottonseed oil, rice oil, peanut oil, and olive oil, and palm oil. , a mixture of 10 to 40% by weight of oils and fats having a carbon atom chain length of 15% or more of one or more types of palmitic acid selected from hydrogenated palm oil, hydrogenated cottonseed oil, hydrogenated rice oil, and hydrogenated kapok oil. , is a method for producing plastic fats and oils that undergoes directed transesterification at 15 to 25°C to obtain fats and oils whose final melting point is maintained at 35 to 45°C. If the above mixing ratio is less than the lower limit or exceeds the upper limit of the range of 60 to 90% by weight of the above liquid vegetable oil and 10 to 40% by weight of oil or fat having a palmitic acid carbon atom chain length of 15% or more, Fats and oils that are the object of this invention cannot be obtained. This mixed oil and fat is subjected to directed transesterification at 15 to 25°C, and the final melting point is 35 to 45°C. Specifically, this is achieved by adjusting the directed transesterification reaction. obtain. In the present invention, the directed transesterification reaction usually requires about 20 hours, but 15 to 20 hours is sufficient. If the reaction temperature is outside the above temperature range, the above reaction will not be carried out properly, which is not preferable. Among the above-mentioned fats and oils having a chain length of 15% or more of palmitic acid carbon atoms, especially palm oil, palm oil itself, partially hydrogenated oil, extremely hardened oil, fractionated oil, fractionated hydrogenated oil, or combinations thereof are selected. You may do so. The palmitic acid content (%) of various oils and fats is shown below. Rapeseed oil 3-4 Soybean oil 9-11 Safflower oil 6-8 Extremely hydrogenated palm oil 40-45 Hardened palm oil 40-45 Palm oil 40-45 Hydrogenated soybean oil 9-11 Hydrogenated cottonseed oil 21-25 Hardened palm kernel oil 8 to 12 Safflower hydrogenated oil 6 to 8 Rice hydrogenated oil 15 to 20 Kapotsu hydrogenated oil 20 to 25 Next, in the present invention, the above-mentioned directed transesterification is a reaction that is carried out with directionality in the exchange reaction, and generally It is carried out in a low temperature range.
It is customary. In this respect, it is contrasted with random transesterification (random reaction), which is generally a reaction at a temperature of 60 to 120°C for 10 to 60 minutes.
On the other hand, in the present invention, the reaction is carried out in a temperature range of 15 to 25° C. while giving directionality to the reaction. It is characterized in that the melting point of the final fat or oil is adjusted to 35 to 45°C. [Function] As is clear from the above explanations and examples, the present invention is capable of producing oils and fats having the above-required oil and fat properties, such as plasticity, by selecting appropriate oils and fats and blending them, and also by direct transesterification of these oils and fats. can get. [Example] The present invention will be specifically described below with reference to Examples. Example 1 800g of rapeseed oil and 200g of hydrogenated palm oil (MP52℃)
After dehydrating under reduced pressure at 100 to 120°C for 1 hour, 0.3% sodium methylate catalyst (based on oil) was added, mixed with stirring, cooled, and kept at a temperature of 20°C for 20 hours. Perform transesterification,
After the reaction is completed, the catalyst is deactivated with water in excess of the equivalent amount, and after sufficient deactivation, the catalyst is heated to 90 to 100°C and decolorized using 2% by weight activated clay in the usual manner. , further blown steam at 240℃ for 1 hour 4.0 (%)
Deodorization was performed to obtain transesterified oil with a melting point of 40°C. 160 g of water, 12 g of salt, 2 g of soybean lecithin, 2 g of glycerin monoglyceride and a small amount of coloring matter were added to 824 g of the obtained transesterified oil and mixed, and after emulsification, margarine for spreads was produced using a small margarine making machine. Examples 2 to 5 In Example 2, the above-mentioned directed transesterification reaction was carried out at 15°C, and in Examples 3 to 5, the reaction was carried out in the same manner as in Example (1) except that the type and composition of the oil and fat were as shown in the following table. Directed transesterified oils were obtained, their melting points are shown in the same table, and margarine for spreads was obtained in the same manner as in Example 1. The properties of the obtained margarine were evaluated and the results are shown in the same table. Comparative Examples 1 to 6 The formulations of each comparative example are as follows. In particular, Comparative Example 2 uses the oil and fat formulation of Example 4, and the reaction is stopped when the temperature reaches 33°C, and Comparative Examples 5 and 6 use the conventional oil/fat formulation. Example 1 was carried out in exactly the same manner as in Example 1, except that the product was manufactured using the oil and fat composition of 1 and no direct ester exchange was performed.

【表】 但し上表中 ○:良好 △:やや良好 × 悪い
上表の結果によれば、実施例1〜5は全て上述
の油脂特性評価を満足して居り、特にマーガリン
の5℃及び30℃下での伸展性が著しく良く、すな
わち温度変化に対して上記適切な対熱性があつて
良好であるのに対して、比較例1〜6は概ね使用
温度範囲が狭く、殆ど実用性に欠けるものであつ
た。 特に実施例4は表の如くサフラワ油80重量%と
パーム硬化油20重量%のダイレクテドエステル交
換であるが、該サフラワー油は多価不飽和脂肪酸
含量が高く飽和脂肪酸量が低いので得られるスプ
レツドマーガリンは多価不飽和脂肪酸リツチ、す
なわちリノール酸含量の高いマーガリンとなり好
ましい。 実施例4の植物油のサフラワ油の代りにヒマワ
リ油を用い(いずれもリノール酸含量が高い)、
これに組合せる第2の油脂がパーム油、綿実油、
カポツク油、米油のいづれかの硬化油を使用して
も同様に好ましい結果を与え得る。液状植物油と
して例示した植物油は上記のナタネ油、大豆油、
サフラワ油、ヒマワリ油と置換しても、いずれも
特に差異は認められず、好結果を得た。 参考例 実施例1の配合すなわちナタネ油80重量%とパ
ーム硬化油(MP52℃)20重量%のダイレクテド
エステル交換反応を30℃、40℃、と高い温度区域
で行つた外は同様に行つたが、その融点はそれぞ
れ30.5℃及び20.3℃で著しく低くダイレクテドエ
ステル交換油脂の適切な硬さが得られず、容易に
油分離を起こし実用性がなかつた。又逆に該反応
温度を5℃、10℃と低い温度区域内で行つたとこ
ろ融点がそれぞれ50.5℃及び48.3℃と高く実用面
で欠ける。以上をまとめると下記の通りである。
[Table] However, in the above table: ○: Good △: Slightly good × Bad According to the results in the above table, Examples 1 to 5 all satisfied the above-mentioned fat property evaluation, especially margarine at 5°C and 30°C. In contrast, Comparative Examples 1 to 6 generally have a narrow operating temperature range and are almost impractical. It was hot. In particular, Example 4 is a directed transesterification of 80% by weight of safflower oil and 20% by weight of hydrogenated palm oil as shown in the table, but this safflower oil can be obtained because it has a high content of polyunsaturated fatty acids and a low content of saturated fatty acids. Spread margarine is preferable because it is rich in polyunsaturated fatty acids, that is, margarine has a high content of linoleic acid. Using sunflower oil instead of safflower oil in the vegetable oil of Example 4 (both have high linoleic acid content),
The second fat to be combined with this is palm oil, cottonseed oil,
Similarly favorable results may be obtained using hydrogenated oils such as kapok oil and rice oil. The vegetable oils exemplified as liquid vegetable oils include the above-mentioned rapeseed oil, soybean oil,
Even when the oil was replaced with safflower oil or sunflower oil, no particular difference was observed in either case, and good results were obtained. Reference example Example 1 was carried out in the same manner as in Example 1, except that the directed transesterification reaction of 80% by weight of rapeseed oil and 20% by weight of hydrogenated palm oil (MP52°C) was carried out at high temperatures of 30°C and 40°C. However, their melting points were extremely low at 30.5°C and 20.3°C, respectively, making it impossible to obtain the appropriate hardness of directed transesterified fats and oils, and oil separation easily occurred, making them impractical. Conversely, when the reaction temperature was carried out in a low temperature range of 5°C and 10°C, the melting points were as high as 50.5°C and 48.3°C, respectively, making them impractical. The above can be summarized as follows.

【表】 [発明の効果] 本発明は以上の説明の如く、従来のマーガリン
等の製造に際して、適切な油脂の選択及び配合組
成、更にこれらのダイレクテドエステル交換反応
により、上記要求される油脂特性即ち可塑性等を
具備した上記問題を解決し得る可塑性油脂を提供
し得るのでありその工業的効果は非常に大きい。
[Table] [Effects of the Invention] As explained above, the present invention achieves the above-mentioned required properties of fats and oils by appropriately selecting and blending the fats and oils, and by direct transesterification thereof, in the production of conventional margarine, etc. That is, it is possible to provide a plastic fat and oil that has plasticity and can solve the above problems, and its industrial effects are very large.

Claims (1)

【特許請求の範囲】[Claims] 1 サフラワ油、ヒマワリ油、大豆油、コーン
油、ナタネ油、綿実油、米油、落花生油、オリー
ブ油から選択された1種又は2種以上の液状植物
油60〜90重量%及びパーム油、パーム硬化油、綿
実硬化油、米硬化油、カポツク硬化油から選択さ
れた1種又は2種以上のパルミチン酸の炭素原子
の鎖長を15%以上有する油脂10〜40重量%の混合
物を、15〜25℃でダイレクテドエステル交換し最
終融点を35〜45℃に保持した油脂を得る可塑性油
脂の製造方法。
1 60 to 90% by weight of one or more liquid vegetable oils selected from safflower oil, sunflower oil, soybean oil, corn oil, rapeseed oil, cottonseed oil, rice oil, peanut oil, and olive oil, and palm oil and hydrogenated palm oil , a mixture of 10 to 40% by weight of one or more palmitic acid carbon atoms having a chain length of 15% or more selected from hydrogenated cottonseed oil, hydrogenated rice oil, and hydrogenated Kapotsu oil. A method for producing plastic fats and oils by direct transesterification at ℃ to obtain fats and oils whose final melting point is maintained at 35 to 45℃.
JP4745586A 1986-03-06 1986-03-06 Production of plastic oils and fats Granted JPS62207399A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4745586A JPS62207399A (en) 1986-03-06 1986-03-06 Production of plastic oils and fats

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4745586A JPS62207399A (en) 1986-03-06 1986-03-06 Production of plastic oils and fats

Publications (2)

Publication Number Publication Date
JPS62207399A JPS62207399A (en) 1987-09-11
JPH0577000B2 true JPH0577000B2 (en) 1993-10-25

Family

ID=12775620

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4745586A Granted JPS62207399A (en) 1986-03-06 1986-03-06 Production of plastic oils and fats

Country Status (1)

Country Link
JP (1) JPS62207399A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3743179B2 (en) * 1998-10-28 2006-02-08 株式会社カネカ Oil composition
JP5924755B2 (en) * 2011-07-29 2016-05-25 日清オイリオグループ株式会社 Method for producing glyceride composition

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49121808A (en) * 1973-03-26 1974-11-21

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS49121808A (en) * 1973-03-26 1974-11-21

Also Published As

Publication number Publication date
JPS62207399A (en) 1987-09-11

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