JPH0577000B2 - - Google Patents
Info
- 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
Links
- 239000003921 oil Substances 0.000 claims description 46
- 235000019198 oils Nutrition 0.000 claims description 46
- 239000003925 fat Substances 0.000 claims description 27
- 235000019482 Palm oil Nutrition 0.000 claims description 13
- 239000002540 palm oil Substances 0.000 claims description 13
- 238000005809 transesterification reaction Methods 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 235000019485 Safflower oil Nutrition 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 239000003813 safflower oil Substances 0.000 claims description 8
- 235000005713 safflower oil Nutrition 0.000 claims description 8
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 7
- 240000007594 Oryza sativa Species 0.000 claims description 6
- 235000007164 Oryza sativa Nutrition 0.000 claims description 6
- 235000009566 rice Nutrition 0.000 claims description 6
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 6
- 239000008158 vegetable oil Substances 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000003549 soybean oil Substances 0.000 claims description 5
- 235000012424 soybean oil Nutrition 0.000 claims description 5
- 235000019486 Sunflower oil Nutrition 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000002600 sunflower oil Substances 0.000 claims description 4
- WVXZNBQXPKNNSC-UHFFFAOYSA-N [C].CCCCCCCCCCCCCCCC(O)=O Chemical group [C].CCCCCCCCCCCCCCCC(O)=O WVXZNBQXPKNNSC-UHFFFAOYSA-N 0.000 claims description 3
- 235000012343 cottonseed oil Nutrition 0.000 claims description 3
- 239000002385 cottonseed oil Substances 0.000 claims description 3
- 239000010514 hydrogenated cottonseed oil Substances 0.000 claims description 3
- 235000019483 Peanut oil Nutrition 0.000 claims description 2
- 235000005687 corn oil Nutrition 0.000 claims description 2
- 239000002285 corn oil Substances 0.000 claims description 2
- 239000004006 olive oil Substances 0.000 claims description 2
- 235000008390 olive oil Nutrition 0.000 claims description 2
- 239000000312 peanut oil Substances 0.000 claims description 2
- 235000019197 fats Nutrition 0.000 description 25
- 238000006243 chemical reaction Methods 0.000 description 12
- 235000013310 margarine Nutrition 0.000 description 12
- 239000003264 margarine Substances 0.000 description 12
- 235000014593 oils and fats Nutrition 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 5
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 244000146553 Ceiba pentandra Species 0.000 description 2
- 235000003301 Ceiba pentandra 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
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- 235000021314 Palmitic acid Nutrition 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 101100472152 Trypanosoma brucei brucei (strain 927/4 GUTat10.1) REL1 gene Proteins 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- 235000014594 pastries Nutrition 0.000 description 2
- 235000015108 pies Nutrition 0.000 description 2
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- 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 1
- 244000020518 Carthamus tinctorius Species 0.000 description 1
- 235000003255 Carthamus tinctorius Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008173 hydrogenated soybean oil Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 229940083466 soybean lecithin Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Landscapes
- Edible Oils And Fats (AREA)
- Fats And Perfumes (AREA)
Description
[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)
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℃.
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)
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)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS49121808A (en) * | 1973-03-26 | 1974-11-21 |
-
1986
- 1986-03-06 JP JP4745586A patent/JPS62207399A/en active Granted
Patent Citations (1)
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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