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JPH0123104B2 - - Google Patents
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JPH0123104B2 - - Google Patents

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Publication number
JPH0123104B2
JPH0123104B2 JP54135367A JP13536779A JPH0123104B2 JP H0123104 B2 JPH0123104 B2 JP H0123104B2 JP 54135367 A JP54135367 A JP 54135367A JP 13536779 A JP13536779 A JP 13536779A JP H0123104 B2 JPH0123104 B2 JP H0123104B2
Authority
JP
Japan
Prior art keywords
fat
butter
melting point
fractionated
temperature
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
Application number
JP54135367A
Other languages
Japanese (ja)
Other versions
JPS5658445A (en
Inventor
Yoshitaka Ebihara
Hiroki Narimatsu
Nobuo Sagi
Kazuo Akamatsu
Hayato Kubota
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.)
Fuji Oil Co Ltd (fka Fuji Oil Holdings Inc)
Original Assignee
Fuji Oil 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 Fuji Oil Co Ltd filed Critical Fuji Oil Co Ltd
Priority to JP13536779A priority Critical patent/JPS5658445A/en
Publication of JPS5658445A publication Critical patent/JPS5658445A/en
Publication of JPH0123104B2 publication Critical patent/JPH0123104B2/ja
Granted legal-status Critical Current

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

Description

【発明の詳細な説明】 本発明は、その特性がカカオ脂と極めて類似し
た優れたハードバター組成物に関する。 周知の如く、カカオバターは製菓用、製パン用
及び製剤用として重要な硬質脂肪の王座を占める
ものであるが、カカオ樹の栽培可能な地域は限ら
れているので、その生産には限りがある。そこで
カカオバターの全部又は一部を置換するための代
用脂には、これまで長年に亘り、研究開発が続け
られながらも、事チヨコレート用代用脂に関して
は、充分満足できるものは出現していない。従
来、カカオ代用脂として開発されてきたハードバ
ターを使用上の点から大別すると、ラウリン系油
脂を主体としたもの、または大豆油の如き液体油
を高度異性化硬化して得られるトランス体酸含量
の高い硬化油で代表されるところの非テンパリン
グ型ハードバターと、2−不飽和−1、3−ジ飽
和トリグリセリド(以下SUSと略す)成分を主
体として含量する天然植物脂肪または、それらの
分画油であるところのテンパリング型ハードバタ
ーとに分けることができる。前者は、カカオ脂と
の組成が根本的に異なるため、カカオ脂と任意の
割合で混合することのできないハードバターであ
るのに対し、後者は組成の点から2−オレオ−
1,3−パルミトステアリンを主とするカカオ脂
と類似しており、一応カカオ脂とは任意の割合で
混合することのできるハードバターである。この
ようなテンパリング型ハードバターに適する天然
植物脂肪として、従来よりパーム油、シア脂、モ
ーラ脂、イリツペ脂、コクム脂、マンゴー核油等
SUS成分を比較的多量含有する脂肪が専ら利
用されてきた。このような脂肪は、ときにはその
ままで使用されるものもあるが、普通は溶剤分別
等の手段により不適当な低融点部或は高融点部を
除去して、カカオ脂と類似のトリグリセリド組成
に富んだ分画油がハードバターとして使用されて
いる。ところが、このようなハードバターは当然
ながらその成分組成がカカオ脂と同じでないた
め、単独で使用されることは少なく、通常はこれ
らのハードバターが適当に配合されて使用され、
特に夏、冬の気温差によつても配合割合は適宜変
更される。このように従来のハードバターには、
融点の高いものから低いものまで種々様々なもの
が存在し、例えば特開昭49−9507号明細書には2
−オレオ−1、3−ジステアリン(SOSと略すこ
とがある)および2−オレオ−パルミトステアリ
ン(POSと略すことがある)の合計量が80〜98
%のトリグリセド成分を含有する硬質脂肪を開示
する。しかしながら、この硬質脂肪の場合、実際
にPOS成分を80%以上含有する脂肪を求めるに
は、カカオ脂を分画するか、あるいは合成手段に
よる以外になく、特に天然植物脂肪に求めること
は、事実上カカオ脂を分画することになり無意味
である。一方、主としてSOS成分を80%以上含有
する脂肪は、前記するシア脂等の植物脂肪の分画
油に求めることは可能であるが、実際にシア脂か
らSOS/POS成分を80%以上含有する分画油を
得ようとすると、収率が40%前後に低下し、副産
物である液体油を多量に副生するため極めて不経
済であるのみでなく、さらに、シア脂の精製に際
しては爽雑するイソプレンポリマーの処理が厄介
な問題となる。しかるに、本発明者らは研究の結
果、サル脂からSUS成分を80〜90%含む分画油
が簡単な手段で70%以上の収率で得られ、かかる
分画油と特定のパーム油中融点画分とを混合して
得たものが、極めてカカオ脂に類似する優れた特
性を有したハードバターになり得るという知見を
得た。本発明はかかる知見に基づいて完成された
ものである。即ち、本発明は主としてパーム油中
融点画分とサル脂固体画分とから成るハードバタ
ーに於いて、パーム油中融点画分として、スリツ
プ融点が29.0゜〜33.0℃、透明点が34℃以下及びサ
ル脂固体画分としてSUS含量が80〜90重量%の
ものを夫々用いることを特徴とするハードバター
組成物である。 本発明において、サル脂固体画分は従来の溶剤
分別法で得られる固体脂画分でよいが、SUS
分を80〜90%(重量基準、以下本明細書中記載の
%は全て重量基準を意味する)含む必要がある。
SUSが下限量未満ではカカオ脂に比べテンパリ
ング温度が低くなり、チヨコレート作業性乃至型
離れが悪化し、さらに耐熱性、シナツプ性も劣る
傾向になる。一方、SUSが上限量を越えても格
別の効果は期待できず、かつ分画のため収量が低
下する。本発明に係るサル脂固体画分(「SAF」
と略すことがある)は、アラキジン酸(C20飽和
脂肪酸)を含むSUS成分を10%以上含有するも
のである。このような結合脂肪酸としてのアラキ
ジン酸は、カカオ脂の主要成分であるPSO(P:
C16飽和脂肪酸、S:C18飽和脂肪酸)に対して、
結合脂肪酸としての炭素数が多いため、カカオ脂
との相溶性が悪いといわれており、事実前掲の特
開昭49−9507号明細書では不純成分として取扱わ
れている。本発明は、このようなアラキジン酸を
結合脂肪酸として含むサル脂固体画分が、特定の
パーム油中融点画分との併用によつて予期し得な
い相剰効果を発揮するものと考えられる。 因みに、かかる効果は、本発明に係るハードバ
ター組成物が第2図及び後記実施例1第1表に示
すように、SCIカーブ及び耐熱性、スナツプ性、
口溶けのいづれの見地においてもカカオ脂に酷似
するのみならず、耐ブルーム性においては、より
優れた特性を有する点からも頷ける。さらに、従
来のハードバターに比べチヨコレート製造時の作
業性が著しく改善されるという効果を有し、これ
は以下の結晶化速度試験及び冷却曲線の測定結果
から覆われる。 〔結晶化速度試験〕 油脂47.8%、ココア51.8%、レシチン0.4%の配
合で、油脂としてカカオバターのみとサル脂分別
脂(SAF)またはシア脂分別脂(SNF)とパー
ム油中融点画分(PMF)との各混合油脂を用い
た品温55℃の配合物を水温26℃の恒温水槽にて撹
拌しながら冷却する。品温40℃をスタートとして
撹拌用プロペラ軸にかかるトルク値の差(トルク
上昇値)を経時的に測定する。粘度上昇の始まる
時間が短かい程、即ち結晶化速度が早くかつ粘度
上昇の傾斜が急激な程チヨコレートのテンパリン
グが容易であるということがいえる。 【表】 この結果、SUS含量84%のサル脂分別脂はカ
カオバターと同等に近い粘度上昇、即ち結晶化速
度を示し、充来のシア脂分別脂よりも優れる。ま
たSUS含量75%のサル脂分別脂はSUS含量が低
く不良であつた。(第1図参照。) 〔冷却曲線〕 試料油12gを温度計を付設した内径16.5mmの試
験管に採取し、60℃に30分間維持した後、これを
内径30mmの外筒試験管に挿入設置し、内径の試料
油が水面下に充分埋設されるまで該外筒試験管を
12℃の恒温水槽に浸漬セツトし、試料温度が50℃
になつたときを0分として、以後1分毎に温度を
記録する。一度下降した温度が最下点に達した後
上昇し、再び下降して一定の間隔で定常となるま
で測定する。ここに上の最下点の温度が高い程テ
ンパリングが容易であり、チヨコレート試作時の
作業性が良好といえる。 【表】 上表に示す如く、融点が略々等しくなる様に配
合した各脂肪について冷却曲線を測定した結果、
SUS含量84%のサル脂分別脂はSUS含量75%の
サル脂分別脂及びシア脂分別脂より最下点が高
く、チヨコレート製造の作業性に優れることを示
唆している。ここにSUS含量84%のサル脂分別
脂は収率70%で得られた分別脂であるのに対し、
シア脂分別脂は収率50%で得られた分別脂であつ
て、本発明が経済的にも優れた特徴を有すること
が窺われる。 かくして、ここに本発明者の認識し得たパーム
油中融点画分(PMFと略すことがある)の好ま
しい特性は、スリツプ融点(SPと略すことがあ
る)が29.0〜33.0℃、透明点(CPと略すことがあ
る)が34℃以下の条件を満足するものである。
SPが上の下限より低くなると、高温時における
製品チヨコレートの硬さが低下し、スナツプ性が
悪化する傾向にあり、逆に上限を越えるとテンパ
リング時粘度上昇を来たし作業性が悪化する傾向
がある。次にCPも上の限昇値を越えるにつれ、
テンパリング時の作業性が悪化する傾向にあるこ
とは、SPの場合と同様である。 以上の目的に適うPMFはパーム油を原料とし
て公知の溶剤分別法により、その高、低両画分を
除去することにより得られるが、常法に比し多少
精密な操作を必要とする。但し、これまでの経験
からすると、予め原料油脂に対し30%以上の低融
点部を除去した後、残部から高融点部分を除去す
るのが収量、品質及び操作の点から最善であるよ
うに見える。この場合、前段の低融点部の除去に
際しては溶媒量を被分別パーム油の2.5〜6倍量
用いるのが良い。分別の温度は溶媒の種類に依り
異なる。例えば、n−ヘキサンでは−10゜〜−17
℃、メチルエチルケトン(MEK)では0゜〜−5
℃の範囲が良い。次段の高融点部の除去の場合も
溶媒量は前段に準じるが、温度は当然、より高温
が好ましく、n−ヘキサンで2゜〜−4℃、MEK
で15゜〜20℃程度が適当である。最後にパーム油
中融点画分中に爽雑する低融点部を除去するに
は、油脂濃度11〜17%として前段の如く操作する
のが良い。なお、溶媒としてアセトンが用いられ
たときは、MEKより多少高い温度を用いるべき
である。いずれにしても、溶媒分別法の原理は油
脂中の各構成グリセリドが融点の差異により一定
温度の溶媒に対する溶解性を異にするという事実
に基づくものであるから、使用する溶媒の種類、
該溶媒中での被分別脂の濃度、冷却速度及び原料
ロツトの相違による品質の振れ等の諸要因に留意
し、経験的に最良の条件を求めるべきである。 以上の分別工程で得たパーム油中融点画分が所
定のSP29.0゜〜33.0℃、CP34℃以下の条件に適合
すれば、これをサル脂固体画分と配合する。因み
にここで規定されたSP及びCPは夫々以下の測定
手段により求められる。 〔S P〕 ASTM DESIGNATION D36−26「瀝青物質
の軟化点測定法」(ASTM STANDARD 1958
PP.1030〜1032記載のリングボール法を準用。但
し測定用鋼球及びリングとして添付図面のものも
のを使用。 〔C P〕 被検油脂約20gを完全溶解し、瀘紙(東洋瀘紙
No.2)で不純物を除いて得た50℃の清澄な試料10
±1gを内径16mm、外径18mm、長さ100mmの試験
管に秤り取り、直ちにストツカー(約−15℃)に
て正確に30分間放置固化させた後、34℃またはそ
れ以上の一定温度に設定した恒温水槽(精度±
0.2℃)中に試料が完全に恒温槽水面下となる様
にセツトして60分間放置した後、試料の状態を観
察して試料全体が透明となつたときは更に設定温
度を下げて、同様の測定を反復し、試料が透明さ
を維持する最低温度を似つて透明点とする。な
お、設定温度で濁りを生じた場合は、当然ながら
前の設定温度より高温の水槽を用いて、同様に測
定を行う。 かくして得られる所定の、SAFとPMFとの混
合比率は25〜75:75〜25の重量比率(但し合計
100)の範囲内にあるのがよく、この範囲内であ
ればカカオ脂に対し、自由な比率で混合すること
ができる。両者の比が1:3より小となれば、テ
ンパリング時の粘度上昇が阻止される反面、製品
チヨコレートの耐熱性あるいは、耐ブルーム性を
低下させる傾向があるので、カカオ脂に対し多量
混用するのが困難となる。一方、上の比が3:1
より大となれば経済的に不得策であるのみでな
く、口溶けが悪化する傾向にあるので、これまた
カカオ脂に対する配合量に制限を受ける。もつと
も、チヨコレート製造時の粘度は配合されるカカ
オマスの量、全脂粉乳の量、粉糖の量及びレシチ
ンなど添加物の量により変化するので、上の比率
は一応の基準を示すのみであり、臨界的意味を有
するものと理解されるべきではない。但し最も好
適と考えられる混合比はPMF:SAF=30:70〜
70:30の範囲であつて、この範囲内のハードバタ
ー組成物は、その融解性状(SCI)がカカオ脂の
それと極めて酷似しており、カカオ脂に対して任
意の比率で配合してもテンパリング時異常な粘度
上昇を起こすことなく、しかも製品チヨコレート
の耐熱性及びスナツプ性あるいは口溶け性共に良
好である。 以下に実施例を掲げ発明実施の態様を述べる。
但し、これらの例は単に例示であつて、発明の限
定を意味するものではない。なお、以下各例にお
けるテンパリングテストは以下の方法で行い、粘
度の変動は材料温度が30℃に達したときの粘度
と、これをさらに設定温度まで冷去後再び昇温さ
せる過程で生じる最大粘度との差(正の粘度変動
値)を撹拌用プロペラ軸にかかるトルク値の差
(トルク上昇値)として記録された。なお、テン
パリングの難易は下記の基準により評価できる。 粘度上昇値 0〜0.7Kg・cm未満 容易 0.7以上1.0Kg・cm未満 比較的容易 1.0以上1.3Kg・cm未満 やや困難 1.3Kg・cm以上 非常に困難 実施例 1 下記配合に従つてカカオバターとSAF、PMF
混合物とのチヨコレート配合テストを行つた。試
作時の粘度上昇は両者間に差異が認められなかつ
た。 〔配合〕 カカオマス 15.6% 全脂粉乳 19.9 粉糖 44.3 油脂1) 19.7 レシチン 0.5 注1) 使用油脂のトリグリセライド組成。 【表】 試作チヨコレートの物性は第1表の如くであつ
て、SAF/PMF混合油脂は口溶け、及び耐熱性、
スナツプ性のいずれの見地においてもカカオバタ
ーと近似し、耐ブルーム性では遥かに優れてい
る。なお、上の混合油脂のSCIカーブは添附図面
のとおりであつて、カカオバターのそれと酷似し
ており、このことからも本混合油脂の優れた性質
が傍証される。 【表】 実施例 2 実施例1のSAFに対し、種々のPMFを一定の
比率に混ぜて実施例1と同様にチヨコレートを試
作評価した。結果は下表(第2表に示される表示
の如く、PMFのSPが29℃以下ではスナツプ性に
欠け、また34℃以上では、テンパリング時の粘度
が顕著に上昇し、作業性が悪化する傾向が見られ
る。 【表】 実施例 3 前例と反対に一定のPMFにSUS含量を異にす
る種々のSAFを配合し、同様にチヨコレートテ
ストを行つた。結果は下表(第3表)に示され
る。表示の如く、SUS含量が80%未満に低下す
ると、チヨコレートとしての物性の低下が見られ
る。なお、本例で用いたPMFはSP32.1℃、
CP33.8℃であつた。 【表】 難易を基準に判定
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to superior hard butter compositions whose properties are very similar to cocoa butter. As is well known, cocoa butter is the most important hard fat used in confectionery, bread making, and pharmaceutical preparations, but since the area where cocoa trees can be grown is limited, its production is limited. be. Therefore, although research and development has been continued for many years on substitute fats for replacing all or part of cocoa butter, a fully satisfactory substitute fat for thiyocolate has not yet appeared. Hard butters that have been developed as cacao substitute fats can be roughly divided into those based on lauric oils and trans-acids obtained by hardening liquid oils such as soybean oil through high isomerization. Non-tempering hard butter, which is typified by hydrogenated oil with a high content, and natural vegetable fats mainly containing 2-unsaturated-1,3-disaturated triglyceride (hereinafter abbreviated as SUS ) components, or their components. It can be divided into tempered hard butter and painting oil. The former is a hard butter that cannot be mixed with cocoa butter in any proportion because its composition is fundamentally different from that of cocoa butter, whereas the latter is a hard butter that cannot be mixed with cocoa butter in any proportion.
It is similar to cacao butter, which mainly contains 1,3-palmitostearin, and is a hard butter that can be mixed with cacao butter in any proportion. As natural vegetable fats suitable for such tempering-type hard butter, fats that contain relatively large amounts of SUS components, such as palm oil, shea butter, mora butter, iritsupe butter, kokum butter, and mango kernel oil, have traditionally been used exclusively. Ta. Although such fats are sometimes used as is, they are usually used by solvent fractionation to remove unsuitable low or high melting point parts to make them rich in triglyceride composition similar to cocoa butter. Fractionated oil is used as hard butter. However, these hard butters naturally do not have the same composition as cacao butter, so they are rarely used alone, and usually these hard butters are mixed appropriately and used.
In particular, the blending ratio is changed as appropriate depending on the temperature difference between summer and winter. In this way, conventional hard butter has
There are various types of melting points ranging from high to low melting points.For example, JP-A-49-9507 describes
-The total amount of oleo-1,3-distearin (sometimes abbreviated as SOS) and 2-oleo-palmitostearin (sometimes abbreviated as POS) is 80 to 98
% of the triglyceride content is disclosed. However, in the case of this hard fat, the only way to obtain a fat that actually contains 80% or more of POS components is to fractionate the cocoa butter or use synthetic means, and it is true that this is especially true for natural vegetable fats. This is meaningless since it involves fractionating the upper cacao fat. On the other hand, fats that mainly contain 80% or more SOS components can be obtained from fractionated oils of vegetable fats such as shea butter, but in reality, fats that contain 80% or more SOS/POS components from shea butter When attempting to obtain fractionated oil, the yield decreases to around 40%, and a large amount of liquid oil is produced as a by-product, which is not only extremely uneconomical, but also requires a lot of filth when refining shea butter. The processing of isoprene polymers becomes a thorny issue. However, as a result of our research, the present inventors have found that a fractionated oil containing 80 to 90% SUS components can be obtained from monkey fat with a yield of 70% or more using simple means. It was found that hard butter obtained by mixing the melting point fraction with the melting point fraction can be made into hard butter with excellent properties extremely similar to cocoa butter. The present invention was completed based on this knowledge. That is, the present invention provides hard butter mainly consisting of a palm oil medium melting point fraction and a sal fat solid fraction. and a hard butter composition characterized in that a monkey fat solid fraction having an SUS content of 80 to 90% by weight is used, respectively. In the present invention, the sal fat solid fraction may be a solid fat fraction obtained by a conventional solvent fractionation method, but the SUS component may be 80 to 90% (by weight; all percentages hereinafter are by weight). meaning) must be included.
If the amount of SUS is less than the lower limit, the tempering temperature will be lower than that of cacao butter, and the workability and mold release of the product will deteriorate, and the heat resistance and synaptability will also tend to deteriorate. On the other hand, even if the amount of SUS exceeds the upper limit, no particular effect can be expected, and the yield will decrease due to fractionation. Sal fat solid fraction (“SAF”) according to the present invention
) contains 10% or more of SUS components including arachidic acid ( C20 saturated fatty acid). Arachidic acid as such a bound fatty acid is a major component of cocoa butter, PSO (P:
C 16 saturated fatty acids, S:C 18 saturated fatty acids),
Because it has a large number of carbon atoms as a bound fatty acid, it is said to have poor compatibility with cacao butter, and in fact is treated as an impure component in the above-mentioned specification of JP-A-49-9507. In the present invention, it is believed that the solid fraction of monkey fat containing arachidic acid as a bound fatty acid exhibits an unexpected synergistic effect when used in combination with a specific mid-melting point fraction of palm oil. Incidentally, this effect is due to the hard butter composition according to the present invention, as shown in FIG. 2 and Table 1 of Example 1, which will be described later.
Not only does it closely resemble cacao butter in terms of melting in the mouth, but it also has superior bloom resistance. Furthermore, it has the effect of significantly improving workability during the production of tyokolate compared to conventional hard butter, and this is confirmed by the following crystallization rate test and cooling curve measurement results. [Crystallization rate test] With a blend of 47.8% oil, 51.8% cocoa, and 0.4% lecithin, the oils are cocoa butter only and monkey fat fractionated fat (SAF) or shea fat fractionated fat (SNF) and palm oil medium melting point fraction ( PMF) and each mixed oil and fat at a temperature of 55°C are cooled with stirring in a constant temperature water bath with a water temperature of 26°C. Starting from a product temperature of 40°C, measure the difference in torque value (torque increase value) applied to the stirring propeller shaft over time. It can be said that the shorter the time at which the viscosity starts to increase, that is, the faster the crystallization rate and the steeper the slope of the viscosity increase, the easier it is to temper the thiokolate. [Table] As a result, the fractionated shea fat with an SUS content of 84% shows a viscosity increase, that is, a crystallization rate similar to that of cocoa butter, and is superior to the conventional fractionated shea fat. Furthermore, the fractionated monkey fat with a SUS content of 75% had a low SUS content and was poor. (See Figure 1.) [Cooling curve] Collect 12 g of sample oil into a test tube with an inner diameter of 16.5 mm equipped with a thermometer, maintain it at 60°C for 30 minutes, and then insert it into an outer test tube with an inner diameter of 30 mm. Place the outer test tube until the inner diameter sample oil is fully buried under the water surface.
Immerse and set the sample in a constant temperature water bath at 12°C until the sample temperature is 50°C.
The temperature is set as 0 minutes, and the temperature is recorded every minute thereafter. Once the temperature has dropped, it reaches the lowest point, rises again, and then measures at regular intervals until it reaches a steady state. It can be said that the higher the temperature at the lowest point on the top, the easier the tempering is, and the better the workability during trial production of Chiyocollate. [Table] As shown in the table above, the results of measuring the cooling curves of each fat blended so that the melting points were approximately the same,
The lowest point of the fractionated monkey fat with an SUS content of 84% is higher than that of the fractionated monkey fat and shea fat with a SUS content of 75%, suggesting that it has superior workability in producing thiokolate. Here, the fractionated monkey fat with an SUS content of 84% is a fractionated fat obtained at a yield of 70%, whereas
The fractionated shea fat is a fractionated fat obtained at a yield of 50%, and it can be seen that the present invention has economically excellent characteristics. Thus, the preferable properties of the palm oil medium melting point fraction (sometimes abbreviated as PMF) that the present inventor has recognized are that the slip melting point (sometimes abbreviated as SP) is 29.0 to 33.0°C, and the clearing point ( (sometimes abbreviated as CP) satisfies the condition of 34℃ or less.
When the SP is lower than the lower limit above, the hardness of the product thiokolate at high temperatures tends to decrease and the snapping properties tend to deteriorate.On the other hand, when it exceeds the upper limit, the viscosity increases during tempering and the workability tends to deteriorate. . Next, as CP exceeds the upper limit increase,
As with SP, workability during tempering tends to deteriorate. PMF suitable for the above purpose can be obtained by using palm oil as a raw material and removing both the high and low fractions using a known solvent fractionation method, but this requires somewhat more precise operations than conventional methods. However, based on past experience, it appears to be best in terms of yield, quality, and operation to first remove 30% or more of the low melting point portion of the raw material oil and fat, and then remove the high melting point portion from the remainder. . In this case, when removing the low melting point portion in the first stage, it is preferable to use a solvent amount 2.5 to 6 times the amount of palm oil to be separated. The temperature for fractionation varies depending on the type of solvent. For example, in n-hexane -10° to -17
°C, 0° to -5 for methyl ethyl ketone (MEK)
Good range of °C. In the case of removing the high melting point part in the next step, the amount of solvent is the same as in the first step, but the temperature is naturally preferably higher, 2° to -4°C with n-hexane, MEK
Approximately 15° to 20°C is appropriate. Finally, in order to remove the coarse low melting point part from the middle melting point fraction of palm oil, it is preferable to operate as in the previous step with an oil concentration of 11 to 17%. Note that when acetone is used as a solvent, a slightly higher temperature than MEK should be used. In any case, the principle of the solvent fractionation method is based on the fact that each component glyceride in fats and oils has different solubility in a solvent at a constant temperature due to the difference in melting point, so the type of solvent used,
The best conditions should be determined empirically, taking into account various factors such as the concentration of the fat to be fractionated in the solvent, the cooling rate, and fluctuations in quality due to differences in raw material lots. If the palm oil medium melting point fraction obtained in the above fractionation process meets the predetermined conditions of SP 29.0° to 33.0°C and CP 34°C or less, it is blended with the monkey fat solid fraction. Incidentally, the SP and CP specified here are each determined by the following measuring means. [S P] ASTM DESIGNATION D36-26 “Softening point measurement method for bituminous materials” (ASTM STANDARD 1958
Apply mutatis mutandis the ring ball method described in PP.1030-1032. However, use the steel balls and rings shown in the attached drawings for measurement. [C P] Completely dissolve approximately 20 g of the oil and fat to be tested, and pour it on filter paper (Toyo Filter Paper).
Clear sample 10 at 50℃ obtained by removing impurities using No. 2)
Weigh ±1g into a test tube with an inner diameter of 16 mm, an outer diameter of 18 mm, and a length of 100 mm. Immediately leave it to solidify in a stocker (approximately -15°C) for exactly 30 minutes, then heat it to a constant temperature of 34°C or higher. Set constant temperature water tank (accuracy ±
After setting the sample completely under the water surface of the constant temperature bath (0.2℃) and leaving it for 60 minutes, observe the condition of the sample. If the entire sample becomes transparent, lower the set temperature further and repeat the same process. The clearing point is determined by repeating the measurement and determining the lowest temperature at which the sample remains transparent. Note that if turbidity occurs at the set temperature, of course, a similar measurement is performed using a water tank with a higher temperature than the previous set temperature. The predetermined mixing ratio of SAF and PMF thus obtained is a weight ratio of 25 to 75:75 to 25 (however, the total
100), and as long as it is within this range, it can be mixed with cacao butter in any ratio. If the ratio of the two is less than 1:3, the increase in viscosity during tempering will be prevented, but it will tend to reduce the heat resistance or bloom resistance of the product, so it is not recommended to mix it in large amounts with cocoa butter. becomes difficult. On the other hand, the ratio above is 3:1
If the amount is larger, it is not only economically disadvantageous, but also tends to deteriorate the meltability in the mouth, which also places restrictions on the amount of cacao butter to be added. However, the viscosity during the production of tyokolate varies depending on the amount of cocoa mass, whole milk powder, powdered sugar, and additives such as lecithin, so the above ratios only provide a rough standard. It should not be understood as having any critical meaning. However, the most suitable mixing ratio is PMF:SAF=30:70~
The ratio is 70:30, and hard butter compositions within this range have a melting property (SCI) very similar to that of cocoa butter, and can be tempered even if blended with cocoa butter at any ratio. There is no abnormal increase in viscosity during processing, and the product thiokolate has good heat resistance, snappability, and meltability in the mouth. Examples are given below to describe the mode of carrying out the invention.
However, these examples are merely illustrative and do not mean a limitation of the invention. In addition, the tempering test in each example below was conducted in the following manner, and the fluctuation in viscosity is determined by the viscosity when the material temperature reaches 30℃, and the maximum viscosity that occurs during the process of cooling it to the set temperature and raising the temperature again. (positive viscosity fluctuation value) was recorded as the difference in torque value applied to the stirring propeller shaft (torque increase value). Note that the difficulty of tempering can be evaluated based on the following criteria. Viscosity increase value 0 to less than 0.7Kg・cm Easy 0.7 or more and less than 1.0Kg・cm Relatively easy 1.0 or more and less than 1.3Kg・cm Slightly difficult 1.3Kg・cm or more Very difficult Example 1 Cocoa butter and SAF according to the following formulation ,PMF
Thiyocolate formulation tests with mixtures were conducted. No difference in viscosity increase was observed between the two during trial production. [Composition] Cocoa mass 15.6% Whole milk powder 19.9 Powdered sugar 44.3 Fats and oils 1) 19.7 Lecithin 0.5 Note 1) Triglyceride composition of the fats and oils used. [Table] The physical properties of the prototype Thiyocolate are as shown in Table 1, and the SAF/PMF mixed oil has melt-in-the-mouth properties, heat resistance,
It is similar to cocoa butter in all aspects of snappability, but far superior in bloom resistance. The SCI curve of the above mixed fat and oil is as shown in the attached drawing, and is very similar to that of cocoa butter, which also supports the excellent properties of this mixed fat and oil. [Table] Example 2 In the same manner as in Example 1, various PMFs were mixed with the SAF of Example 1 at a fixed ratio to produce and evaluate a prototype of Chiyocolate. The results are shown in the table below (as shown in Table 2, when the SP of PMF is below 29℃, snapping properties are lacking, and when it is above 34℃, the viscosity during tempering increases markedly, and workability tends to deteriorate. [Table] Example 3 Contrary to the previous example, various SAFs with different SUS contents were mixed with a constant PMF, and a similar thiokolate test was conducted.The results are shown in the table below (Table 3). As shown in the display, when the SUS content decreases to less than 80%, a decrease in the physical properties of thiyocholate is observed.The PMF used in this example has an SP of 32.1℃,
CP was 33.8℃. [Table] Judgment based on difficulty

【図面の簡単な説明】[Brief explanation of drawings]

第1図は、カカオバターAと本発明範囲内のサ
ル脂分別脂とパーム油中融点画分との混合物B、
シア脂分別脂とパーム油中融点画分との混合物C
及び本発明範囲外のサル脂分別脂とパーム油中融
点画分との混合物Dとを、ココア及びレシチンと
一定割合で配合した配合物の結晶化速度試験のグ
ラフである。第2図は、カカオバターA及び本発
明に係るハードバターとパーム油中融点画分との
等量混合物BのSCIカーブである。第3図は本発
明におけるスリツプ融点の測定に使用される鋼球
の拡大正面図、第4図は同じく鋼リングの同率拡
大平面図、第5図は第4図A−A線に沿う断面図
である。図中の各寸法は以下のとおりであり、か
つ第3図の鋼球の重量は以下のとおりである。 鋼球の重量= 3.50〜 3.55g d1=10.50〜10.55mmφ d2=20.00〜20.50mmφ d3=17.50〜18.00mmφ d4=15.50〜16.00mmφ t1= 6.00〜 6.50mm t2= 4.00〜 4.50mm t3= 0.50mm
FIG. 1 shows a mixture B of cocoa butter A, sal fat fractionated fat within the scope of the present invention, and palm oil medium melting point fraction;
Mixture C of fractionated shea fat and palm oil medium melting point fraction
It is a graph of a crystallization rate test of a mixture in which a mixture D of monkey fat fractionated fat outside the scope of the present invention and a palm oil medium melting point fraction is blended with cocoa and lecithin at a constant ratio. FIG. 2 is the SCI curve of cocoa butter A and an equal mixture B of hard butter and palm oil medium melting point fraction according to the invention. FIG. 3 is an enlarged front view of a steel ball used for measuring the slip melting point in the present invention, FIG. 4 is an enlarged plan view of a steel ring, and FIG. 5 is a cross-sectional view taken along the line A-A in FIG. It is. Each dimension in the figure is as follows, and the weight of the steel ball in FIG. 3 is as follows. Weight of steel ball = 3.50 ~ 3.55g d1 = 10.50 ~ 10.55mmφ d2 = 20.00 ~ 20.50mmφ d3 = 17.50 ~ 18.00mmφ d4 = 15.50 ~ 16.00mmφ t1 = 6.00 ~ 6.50mm t2 = 4.00 ~ 4.50mm t3 = 0 .50mm

Claims (1)

【特許請求の範囲】[Claims] 1 主としてパーム油中融点画分とサル脂固体画
分とから成るハードバターに於いて、パーム油中
融点画分としてスリツプ融点が29.0゜〜33.0℃透明
点が34℃以下及びサル脂固体画分として2−不飽
和−1、3−ジ飽和トリグリセリド含量が80〜90
重量%のものを夫々用いることを特徴とするハー
ドバター組成物。
1. In hard butter mainly consisting of palm oil medium melting point fraction and monkey fat solid fraction, the palm oil medium melting point fraction has a slip melting point of 29.0° to 33.0°C, a clearing point of 34°C or less, and monkey fat solid fraction. As 2-unsaturated-1,3-disaturated triglyceride content is 80-90
% by weight of each hard butter composition.
JP13536779A 1979-10-19 1979-10-19 Hard butter composition Granted JPS5658445A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13536779A JPS5658445A (en) 1979-10-19 1979-10-19 Hard butter composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13536779A JPS5658445A (en) 1979-10-19 1979-10-19 Hard butter composition

Publications (2)

Publication Number Publication Date
JPS5658445A JPS5658445A (en) 1981-05-21
JPH0123104B2 true JPH0123104B2 (en) 1989-05-01

Family

ID=15150066

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13536779A Granted JPS5658445A (en) 1979-10-19 1979-10-19 Hard butter composition

Country Status (1)

Country Link
JP (1) JPS5658445A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0464881A1 (en) * 1990-06-14 1992-01-08 Unilever N.V. Improved coatings
JP3371465B2 (en) * 1993-05-21 2003-01-27 鐘淵化学工業株式会社 Melting chocolates

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS533568A (en) * 1976-06-30 1978-01-13 Asahi Denka Kogyo Kk Cacao fat substitute
JPS53111307A (en) * 1977-03-11 1978-09-28 Asahi Denka Kogyo Kk Cacao butter substitute
JPS53115863A (en) * 1977-03-18 1978-10-09 Asahi Denka Kogyo Kk Cacao substitute oil
JPS5918969B2 (en) * 1977-09-08 1984-05-01 不二製油株式会社 hard butter composition

Also Published As

Publication number Publication date
JPS5658445A (en) 1981-05-21

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