JPS62295996A - Production of plastic oils and fats - Google Patents
Production of plastic oils and fatsInfo
- Publication number
- JPS62295996A JPS62295996A JP13838686A JP13838686A JPS62295996A JP S62295996 A JPS62295996 A JP S62295996A JP 13838686 A JP13838686 A JP 13838686A JP 13838686 A JP13838686 A JP 13838686A JP S62295996 A JPS62295996 A JP S62295996A
- Authority
- JP
- Japan
- Prior art keywords
- oil
- fats
- oils
- fat
- margarine
- 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.)
- Granted
Links
- 235000014593 oils and fats Nutrition 0.000 title claims description 8
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 239000003921 oil Substances 0.000 claims description 44
- 235000019198 oils Nutrition 0.000 claims description 44
- 239000003925 fat Substances 0.000 claims description 26
- 238000005809 transesterification reaction Methods 0.000 claims description 15
- 238000002844 melting Methods 0.000 claims description 12
- 230000008018 melting Effects 0.000 claims description 12
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 9
- 235000019485 Safflower oil Nutrition 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- 239000003813 safflower oil Substances 0.000 claims description 9
- 235000005713 safflower oil Nutrition 0.000 claims description 9
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 8
- 239000008158 vegetable oil Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 4
- 235000019486 Sunflower oil Nutrition 0.000 claims description 3
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 claims description 3
- 239000008164 mustard oil Substances 0.000 claims description 3
- 239000002600 sunflower oil Substances 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 230000000717 retained effect Effects 0.000 claims 1
- 235000019197 fats Nutrition 0.000 description 23
- 235000013310 margarine Nutrition 0.000 description 16
- 239000003264 margarine Substances 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- JLPULHDHAOZNQI-ZTIMHPMXSA-N 1-hexadecanoyl-2-(9Z,12Z-octadecadienoyl)-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC JLPULHDHAOZNQI-ZTIMHPMXSA-N 0.000 description 2
- 240000002791 Brassica napus Species 0.000 description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 2
- 241001137251 Corvidae Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 235000015108 pies Nutrition 0.000 description 2
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 229940083466 soybean lecithin Drugs 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 description 1
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 description 1
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- WVXZNBQXPKNNSC-UHFFFAOYSA-N [C].CCCCCCCCCCCCCCCC(O)=O Chemical group [C].CCCCCCCCCCCCCCCC(O)=O WVXZNBQXPKNNSC-UHFFFAOYSA-N 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 150000002148 esters Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 235000014594 pastries Nutrition 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Landscapes
- Edible Oils And Fats (AREA)
- Fats And Perfumes (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
3、発明の詳細な説明
(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、特にスプレッド
性(IllI展性)が要求されるマーガリン、ショー1
−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。Detailed Description of the Invention 3. Detailed Description of the Invention (Industrial Field of Application) The present invention relates to a method for producing plastic fats and oils, and particularly margarine that requires spreadability (IllI malleability), Show 1
The present invention relates to a method for producing plastic fats and oils suitable for use in coatings, edible processing fats and oils, and the like.
(従来の技術)
一般にマーガリン、ノヨー;・ニンゲ等に対シテは、そ
れらの食用時及び調理時等に安定したスプレッド性が要
求されるが、かがるスプレッド性が要求されろ油脂は、
通常例えばサフラワ油、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。(Prior art) In general, stable spreadability is required for margarine, oils and fats when eating and cooking them, but oils and fats that require thick spreadability are
It is usually manufactured by blending, for example, safflower oil, soybean oil, rapeseed oil, their hydrogenated oils, etc. to have an appropriate consistency (plasticity).
(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
ろ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った。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
スプレッド性が要求され製品は、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
1史用される温度範囲で適切な可塑性等緒特性を具備し
ていることが強く望まれている。(Problems to be Solved by the Invention) However, it has been pointed out that such oils and fats have relatively narrow temperature ranges in which the above-mentioned plasticity can be maintained appropriately, and that there are problems such as insufficient relatively constant shape retention. there were. In other words, shape retention is considered to be similar to heat resistance, and the products that require spreadability include pies, pastries, and household margarine, all of which have been used for a long time. It is strongly desired that the material has appropriate plasticity and other properties in the temperature range.
発明者等は先に、液状植物油60〜90wt%、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1
0〜40 w t%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を提案し、上述の問
題を著しく改善し多大の成果を収めた。The inventors have previously developed an oil and fat 1 containing 60 to 90 wt% of liquid vegetable oil and 15% or more of the chain length of palmitic acid carbon atoms.
We proposed a method for producing plastic fats and oils by direct transesterification of a mixture of 0 to 40 wt% at 15 to 25°C to obtain an oil with a final melting point of 35 to 45°C, which significantly improved the above-mentioned problems and brought about significant improvements. achieved results.
ただこの方法ではエステル交換の1度範囲が狭く、物性
選択の範囲がある程度限定される等の尚解決を要する問
題があった。However, this method has problems that still need to be resolved, such as the narrow range of one degree of transesterification and the range of selection of physical properties.
(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、特に使用温度中が広くす
なわち温度変化に対して耐熱性があり、そして安定した
スプレッド性のある特にパイ、ベストリー用及び家庭用
食卓マーガリンに要求されろ可塑性油脂に関し継続して
検討を重ねた結果、特定の第2の油脂の他の選択により
上記ダイレクテドエステル交換の1度範囲が低温側に拡
大されろことを見出し本発明を完成するに至ったのであ
る。(Means for Solving the Problems) The present inventors have found that among the above-mentioned oil and fat properties, it has a wide usage temperature range, that is, it is heat resistant to temperature changes, and has stable spreadability, especially for pies and vestries. As a result of continued studies regarding the plastic fats and oils required for household table margarine, we have found that the 1 degree range of the above-mentioned directed transesterification can be expanded to the lower temperature side by selecting other specific second fats and oils. This has led to the completion of the present invention.
即ち本発明は、液状植物油75〜95 w t%、及び
ペヘン酸の炭素原子の鎖長を10%以上有する油脂5〜
25wt%の混合物を、10〜25℃でグイレクテドエ
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。That is, the present invention provides liquid vegetable oils containing 75 to 95 wt% and 5 to 95 wt% of oils and fats having a chain length of 10% or more of the carbon atoms of phenic acid.
This is a method for producing plastic fats and oils in which a 25 wt% mixture is subjected to gilected transesterification at 10 to 25°C to obtain fats and oils whose final melting point is maintained at 35 to 45°C.
本発明において、上記液状植物油とは、例えば、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、オリーブ油等から選択された1種
又は2種以上の植物油を意味し、これらは75〜95w
t%が好適である。モして又、本発明においてペヘン酸
(炭素数20゜二重結合0個)の炭素原子の鎖長を10
%以上有する油脂としては、からし硬化油、ナタネ硬化
肋の1種あるいはこれらの2種以上の混合油脂を意味し
、その5〜25wt%が上記液状油脂と混合される。こ
こでナタネ硬化油とは、品種改良前のナタネ油の硬化油
を意味し、エルシン酸(炭素数22、二重結合1個)型
に富むナタネ肋の硬化油である。これらの混合比、即ち
上記液状植物油75〜95wt%及びペヘン酸の炭素原
子の鎖長を10%以上有する油脂5〜25wt%の範囲
の下限未満あるいはその上限を超えろ場合には、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。In the present invention, the liquid vegetable oil refers to one or more vegetable oils selected from, for example, safflower oil, sunflower oil, soybean oil, corn oil, rapeseed oil, cottonseed oil, rice oil, peanut oil, olive oil, etc. meaning, these are 75~95w
t% is preferred. Furthermore, in the present invention, the chain length of carbon atoms of phenic acid (20 carbon atoms, 0 double bonds) is 10
% or more means one type of hardened mustard oil, hardened rapeseed oil, or a mixture of two or more of these, and 5 to 25 wt% of the oil is mixed with the liquid oil. Here, rapeseed hydrogenated oil means hydrogenated oil of rapeseed oil before breeding, and is hydrogenated oil of rapeseed ribs rich in erucic acid (22 carbon atoms, 1 double bond) type. If the mixing ratio of these is less than the lower limit or exceeds the upper limit of the range of 75 to 95 wt% of the liquid vegetable oil and 5 to 25 wt% of the oil and fat having a carbon atom chain length of pehenic acid of 10% or more, the present invention The desired oils and fats cannot be obtained.
この混合油脂は10〜25℃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
整することによって達成し得る。Direct transesterification of this mixed fat and oil is carried out at 10 to 25°C so that its final melting point is 35 to 45°C, which can be specifically achieved by adjusting the directed transesterification.
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。In the present invention, the directed transesterification reaction includes:
It usually takes 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.
次に本発明において上記ダイレクテドエステル交換1よ
咳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、10
〜25℃の1度区域で反応に指向性を与えて行われる。Next, in the present invention, the above-mentioned directed transesterification 1 is a reaction carried out with directionality during the exchange reaction,
Generally, it is customary to carry out the process at low temperatures. This is in contrast to random transesterification, i.e., generally at a temperature of 60 to 120°C;
The reaction lasted for ~60 minutes. In contrast, the present invention provides 10
The reaction is carried out in a 1 degree zone at ~25°C to give directionality to the reaction.
そして最終油脂の融点が35〜45℃に調整されろ点に
特長を有する。The melting point of the final oil and fat is adjusted to 35 to 45°C, and has the characteristic of a filter point.
(作 用)
不発明は上記の説明及び実施例で明らかなように適切な
第2の油脂の選択及び配合組成、更にこれらのグイレク
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。(Function) As is clear from the above description and examples, the invention is based on the selection and blending composition of an appropriate second oil and fat, and furthermore, through the glycated transesterification reaction, the above-mentioned required oil and fat properties, such as plasticity, etc., can be achieved. An oil or fat containing the following can be obtained.
(実 施 例〕 以下実施例によりこの発明を具体的に説明する。(Example〕 The present invention will be specifically explained below with reference to Examples.
実施例1〜5
サフラワ油900gとナタネ極度硬化油(MP62℃)
100gとを混合し100〜120℃で1時間減圧下で
脱水を行なったのち触媒ナトリウムメチラート0.3%
(対油)加丸て撹拌混合し冷却し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、当社より過剰の水で触媒を失活させ、該失活を十
分に行なった後、90〜100℃まで加温し2 w t
%活性白土を使用して常法通り脱色を行ない、更に24
0℃1時間吹込み蒸気4.0(%)で脱臭を行ない融点
43.0℃のエステル交換油を得た。Examples 1-5 900g of safflower oil and extremely hardened rapeseed oil (MP62°C)
After mixing with 100g and dehydrating under reduced pressure at 100-120℃ for 1 hour, 0.3% of sodium methylate catalyst was added.
(For oil) Mix with stirring, cool and maintain the temperature at 20℃ to perform directed ester exchange for 20 hours. After the reaction is complete, we deactivate the catalyst with excess water from our company and sufficiently deactivate it. After heating to 90-100℃, 2wt
Decolorization was carried out in the usual manner using % activated clay, and further 24%
Deodorization was carried out with 4.0 (%) steam blown in for 1 hour at 0°C to obtain transesterified oil with a melting point of 43.0°C.
得られたエステル交換油824gに、水160g1食塩
12g1大豆レシチン2g1グリセリ〉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ッド用マーガリンを製造した。To 824 g of the obtained transesterified oil were added 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, and after emulsification, margarine for spread was produced using a small margarine making machine.
実施例2ば上記グイレクテドエステル交換反応を10℃
で行い、又実施例3〜5は油脂の種類及び配合を次表の
如くした外は上記実施例(11と同様に行いグイレクテ
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ッド用マーガリ
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。Example 2 The above gilected transesterification reaction was carried out at 10°C.
Examples 3 to 5 were carried out in the same manner as in Example 11 above, except that the types and compositions of the oils and fats were as shown in the following table. Furthermore, margarine for spread was obtained in the same manner as in Example 1. The characteristics of the obtained margarine were evaluated and the results are shown in the table.
比較例1〜6
各比較例中、特に比較例3,4は表示の融点に達したと
きに反応を停止させ、又比較例5,6は従来の油脂配合
で製造したものでグイレクテドエステル交換は行なって
いない外は実施例(1)と全く同様に行なった。Comparative Examples 1 to 6 Among the comparative examples, especially in Comparative Examples 3 and 4, the reaction was stopped when the indicated melting point was reached, and in Comparative Examples 5 and 6, the reaction was produced using a conventional oil/fat blend. The procedure was carried out in exactly the same manner as in Example (1) except that no exchange was performed.
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耐熱性があって良好であるのに
対して、比較例+11〜(6)は概ね使用温度範囲が狭
く、殆んど実用性に欠けるものであった。According to the results in the table above, Examples (1) to (5) all satisfied the above-mentioned fat and oil property evaluation, and especially margarine 5.
℃ and 30 ℃, that is, the appropriate heat resistance against temperature changes is good, whereas Comparative Examples +11 to (6) generally have a narrow usage temperature range. Most of them lacked practicality.
特に実施例2は表の如くサフラワ油95wt%とナタネ
極度硬化油5wt%のダイレクテドエステル交換である
が、該サフラワ油は多価不飽和脂肪酸含量が高く飽和脂
肪酸含量が低いので得られろスプレッドマーガリンは多
価不飽和脂肪酸リッチ、すなわちリノール酸含量が一段
と高いマーガリンとなり好ましい。In particular, Example 2 is a direct transesterification of 95 wt% safflower oil and 5 wt% extremely hardened rapeseed oil as shown in the table, but since the safflower oil has a high polyunsaturated fatty acid content and a low saturated fatty acid content, it is difficult to obtain a spread. Margarine is preferable because it is rich in polyunsaturated fatty acids, that is, margarine has a higher content of linoleic acid.
上記植物油がサフラワ油の代りにヒマワリ油、こねに組
合せる第2の油脂がナタネ油、カラシ油いづれかの硬化
油であっても同様に好ましい結果を与又碍ろ。Even if the above-mentioned vegetable oil is sunflower oil instead of safflower oil, and the second oil and fat combined in the kneading is a hydrogenated oil such as rapeseed oil or mustard oil, similar favorable results can be obtained.
参考例
実施例4の配合すなわちサフラワ油90 w t%と、
ナタネ極度硬化油(MP63℃)10wt%のダイレ々
テドエステル交換反応を30℃、40℃と高いl温度区
域で行った外は同様に行ったが、その融点はそれぞれ3
2.6℃及び22.5℃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った。文通に該反応温度を5℃の伝
い温度で行ったところ融点が51.6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。Reference Example The formulation of Example 4, ie 90 wt% of safflower oil,
The diester transesterification reaction of 10 wt% of extremely hardened rapeseed oil (MP63°C) was carried out in the same manner except that it was carried out in the high temperature range of 30°C and 40°C, but the melting point was 3.
The hardness was extremely low at 2.6°C and 22.5°C, making it impossible to obtain an appropriate hardness for the directed transesterified oil and oil, which easily caused oil separation, making it impractical. When the reaction was carried out at a temperature of 5° C., the melting point was as high as 51.6, which is not practical. The above can be summarized as follows.
次に実施例(4)のダイレクテドエステル交換油を使用
してスプレッドマーガリンを製造した。即ちグイレクテ
ドエステル交換油319g、パーム核極度硬化油49g
、サフラワ油450 g、水170g1食塩10g、大
豆レシチン1.0g及び色素少量を加丈て混和し、乳化
した後、小型マーガリン製造機でスプレッド用マーガリ
ンを製造した。得られたマーガリンの融点は33.5℃
、5℃、30′℃の伸展性及び口溶けは実用的に満足す
べきものであった。Next, spread margarine was produced using the directed transesterified oil of Example (4). Namely, 319 g of gilected transesterified oil, 49 g of extremely hardened palm kernel oil.
, 450 g of safflower oil, 170 g of water, 10 g of salt, 1.0 g of soybean lecithin, and a small amount of color were mixed and emulsified, and then margarine for spread was produced using a small margarine making machine. The melting point of the resulting margarine was 33.5℃
, 5°C and 30'°C, and melting in the mouth were practically satisfactory.
(発明の効果)
本発明は以上の如く、適切な油脂の選択により上記グイ
レクテドエステル交換反応の温度範囲を拡げ得るのであ
り、この結果上記要求されろ油脂特性即ち可塑性等物性
を幅広く選択し得る。(Effects of the Invention) As described above, the present invention makes it possible to widen the temperature range of the gilected transesterification reaction by selecting an appropriate oil and fat, and as a result, the required oil and fat properties, that is, physical properties such as plasticity, can be selected from a wide range. obtain.
更にこの発明による油脂は、適切に可塑性を保持する温
度範囲が非常に広く、シかも融点が高い割りには口溶け
が良好であり、この7ItI脂のみによる場合は勿論、
配合油の一部に使用してもマーガリン、ンヨートニング
あるいは食用加工油脂等の可塑性油脂を改良し得るので
ある。Furthermore, the oil and fat according to the present invention has a very wide temperature range in which it maintains its plasticity appropriately, and melts well in the mouth despite its high melting point.
Even if it is used as part of a blended oil, it can improve the plasticity of margarine, toning, or edible processed fats and oils.
Claims (2)
素原子の鎖長を10%以上有する油脂5〜25wt%の
混合物を、10〜25℃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) A mixture of 75 to 95 wt% of liquid vegetable oil and 5 to 25 wt% of oils and fats having a chain length of pehenic acid carbon atoms of 10% or more is subjected to direct transesterification at 10 to 25°C to achieve a final melting point of 35 to 45°C. A method for producing plastic fats and oils that obtains fats and oils that are retained.
これに混合する第2の油脂がナタネ油、カラシ油の群か
ら選択される(1)項記載の方法。(2) the liquid vegetable oil is a group of safflower oil and sunflower oil;
The method according to item (1), wherein the second fat and oil mixed therein is selected from the group of rapeseed oil and mustard oil.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13838686A JPS62295996A (en) | 1986-06-16 | 1986-06-16 | Production of plastic oils and fats |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13838686A JPS62295996A (en) | 1986-06-16 | 1986-06-16 | Production of plastic oils and fats |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62295996A true JPS62295996A (en) | 1987-12-23 |
JPH0575038B2 JPH0575038B2 (en) | 1993-10-19 |
Family
ID=15220727
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13838686A Granted JPS62295996A (en) | 1986-06-16 | 1986-06-16 | Production of plastic oils and fats |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62295996A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995007619A1 (en) * | 1993-09-14 | 1995-03-23 | Loders Croklaan B.V. | Healthy spread fats |
JP2013028752A (en) * | 2011-07-29 | 2013-02-07 | Nisshin Oillio Group Ltd | Method for producing glyceride composition |
JP2016208973A (en) * | 2015-05-01 | 2016-12-15 | 太陽油脂株式会社 | Fat composition for producing household margarine |
-
1986
- 1986-06-16 JP JP13838686A patent/JPS62295996A/en active Granted
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995007619A1 (en) * | 1993-09-14 | 1995-03-23 | Loders Croklaan B.V. | Healthy spread fats |
JP2013028752A (en) * | 2011-07-29 | 2013-02-07 | Nisshin Oillio Group Ltd | Method for producing glyceride composition |
JP2016208973A (en) * | 2015-05-01 | 2016-12-15 | 太陽油脂株式会社 | Fat composition for producing household margarine |
Also Published As
Publication number | Publication date |
---|---|
JPH0575038B2 (en) | 1993-10-19 |
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