JP5493862B2 - Chocolate additive and method for producing the same - Google Patents

Chocolate additive and method for producing the same Download PDF

Info

Publication number
JP5493862B2
JP5493862B2 JP2009540042A JP2009540042A JP5493862B2 JP 5493862 B2 JP5493862 B2 JP 5493862B2 JP 2009540042 A JP2009540042 A JP 2009540042A JP 2009540042 A JP2009540042 A JP 2009540042A JP 5493862 B2 JP5493862 B2 JP 5493862B2
Authority
JP
Japan
Prior art keywords
chocolate
fat
additive
oil
parts
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.)
Active
Application number
JP2009540042A
Other languages
Japanese (ja)
Other versions
JPWO2009060809A1 (en
Inventor
和寿 山田
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
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 JP2009540042A priority Critical patent/JP5493862B2/en
Publication of JPWO2009060809A1 publication Critical patent/JPWO2009060809A1/en
Application granted granted Critical
Publication of JP5493862B2 publication Critical patent/JP5493862B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23GCOCOA; COCOA PRODUCTS, e.g. CHOCOLATE; SUBSTITUTES FOR COCOA OR COCOA PRODUCTS; CONFECTIONERY; CHEWING GUM; ICE-CREAM; PREPARATION THEREOF
    • A23G1/00Cocoa; Cocoa products, e.g. chocolate; Substitutes therefor
    • A23G1/30Cocoa products, e.g. chocolate; Substitutes therefor
    • A23G1/32Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds
    • A23G1/36Cocoa products, e.g. chocolate; Substitutes therefor characterised by the composition containing organic or inorganic compounds characterised by the fats used

Description

本発明は、従来の製造方法よりも簡便な方法で製造することが可能な、テンパリング促進効果及びファットブルーム抑制効果を有するチョコレート添加剤およびその製造方法に関するものである。 The present invention relates to a chocolate additive having a tempering promoting effect and a fat bloom suppressing effect, which can be produced by a simpler method than a conventional production method, and a production method thereof.

一般に、ココアバターやココアバターに代用して使用されるハードバターを使用した、いわゆるテンパリング型チョコレートの製造には、テンパリング処理により、チョコレート中のココアバター等の油脂を安定な結晶型に移行させ固化させることが重要であり、テンパリングが不十分であると、保存中にファットブルームと呼ばれるチョコレート表面の白化現象が起き、チョコレートの口溶け、滑らかさ等の食感が著しく損なわれてしまう。 In general, in the production of so-called tempering type chocolate using hard butter used in place of cocoa butter or cocoa butter, the fats and oils such as cocoa butter in chocolate are transferred to a stable crystal form and solidified by tempering treatment. If the tempering is insufficient, a whitening phenomenon of the chocolate surface called fat bloom occurs during storage, and the texture such as melting of the mouth of the chocolate and smoothness are remarkably impaired.

そのため、チョコレートの工業的生産において、融解したチョコレートを冷却し、さらに再度加温(リヒート)しなければならないテンパリング工程は、非常に複雑な工程のため、テンパリングが不十分となり、製造後のチョコレート製品が流通、保存段階において極端な温度変化をうけると、ファットブルームが発生し、商品価値を著しく損なうといった問題がしばしば発生する。 Therefore, in the industrial production of chocolate, the tempering process in which the melted chocolate must be cooled and then reheated (reheated) is a very complicated process, so the tempering is insufficient and the chocolate product after production However, when an extreme temperature change occurs in the distribution and storage stages, fat blooms often occur and the commercial value is significantly impaired.

さらに、チョコレートが体温を越えるような高温に一定時間曝される場合には、いかに良好なテンパリング処理を行ってもファットブルームの発生を防止することは困難である。 Furthermore, when chocolate is exposed to a high temperature exceeding body temperature for a certain period of time, it is difficult to prevent the occurrence of fat bloom no matter how good the tempering treatment is performed.

そこで、従来から、このような複雑なテンパリング工程を省略ないしは簡略化したチョコレート製造方法として、微粉砕化したチョコレートの粉末、ココアバターの粉末、または、特定のトリグリセリド組成をもつ油脂の粉末を、溶融したチョコレート組成物に添加混合して製造する方法がある。このようなチョコレートの製造法は、通常シーディング法と呼ばれており、近年、ココアバターのトリグリセリド組成に類似させた特定のグリセリド組成物を添加する方法が開発されており、また、製品チョコレートが体温付近の高温に、一定時間曝される場合のファットブルームを防止する方法として、粉末状粒子のチョコレート添加剤を用いる方法も提案されている。(特許文献1〜3) Therefore, conventionally, as a chocolate manufacturing method in which such a complicated tempering process is omitted or simplified, finely pulverized chocolate powder, cocoa butter powder, or fat powder having a specific triglyceride composition is melted. There is a method of adding and mixing to the chocolate composition. Such a chocolate production method is usually called a seeding method, and in recent years, a method of adding a specific glyceride composition similar to the triglyceride composition of cocoa butter has been developed. As a method for preventing fat bloom when exposed to a high temperature near body temperature for a certain period of time, a method using a chocolate additive of powdery particles has also been proposed. (Patent Documents 1 to 3)

しかしながら、これら粉末状のチョコレート添加剤は、みかけ比重が軽いため、十分な攪拌を行わないと、粘性のあるチョコレート中にはチョコレート添加剤が均一に分散せず、テンパリングが不十分となることもあり、改善の余地があった。 However, these powdery chocolate additives have a low apparent specific gravity, and unless sufficient agitation is performed, the chocolate additive may not be uniformly dispersed in the viscous chocolate, resulting in insufficient tempering. There was room for improvement.

この問題を改善する方法として、チョコレートに添加した際に、容易に分散できるような、液状油ベースのチョコレート添加剤が提案されている(特許文献4)が、液状油ベースのチョコレート添加剤の場合、その製造工程において、液状の油に油脂結晶を均一に分散させることは容易でなく、チョコレート添加剤の製造効率に問題があった。 As a method for improving this problem, a liquid oil-based chocolate additive that can be easily dispersed when added to chocolate has been proposed (Patent Document 4), but in the case of a liquid oil-based chocolate additive In the production process, it is not easy to uniformly disperse the fat crystals in the liquid oil, and there is a problem in the production efficiency of the chocolate additive.

また、チョコレート添加剤がテンパリング促進機能を発揮するためには、チョコレート添加剤中に、安定型結晶に転移した状態で油脂結晶が存在していることが必要であるが、従来のチョコレート添加剤の製造方法では、あらかじめ安定型に転移した油脂結晶粉末を調製する工程が必要であった。 In addition, in order for the chocolate additive to exhibit the tempering promoting function, it is necessary that the fat and oil crystals are present in the chocolate additive in a state of being transferred to a stable crystal. In the production method, a step of preparing a fat crystal powder that has been transferred to a stable type in advance is required.

油脂結晶を安定型に転移させるためには、油脂結晶を安定型結晶の融点より少し低い温度で、長い時間をかけて転移させる工程が必須である。特に油脂を構成する脂肪酸が炭素数20以上の長鎖飽和脂肪酸を含む場合、その傾向は著しく、安定型結晶を得るためには、高温かつ長時間の結晶転移工程を経ることになり、製造コストの上昇をもたらしている。 In order to transfer the fat and oil crystals to a stable type, a step of transferring the fat and oil crystals over a long time at a temperature slightly lower than the melting point of the stable type crystals is essential. In particular, when the fatty acid constituting the fat contains a long-chain saturated fatty acid having 20 or more carbon atoms, the tendency is remarkable, and in order to obtain a stable crystal, a high-temperature and long-time crystal transition step is required, resulting in a production cost. Has brought rise.

油脂結晶の安定化を促進させる方法として、油脂の結晶化直前に5MPa/秒以上の加圧速度で10〜50MPaまで急速に加圧することで、微細で安定な結晶を短時間で得る方法(特許文献5)や油脂の結晶化工程でパルス磁場処理を行い、油脂の結晶化を促進または安定化させる方法(特許文献6)が提案されているが、これらの方法はいずれも、高圧処理や強力なパルス磁場を行う装置が必要となるため、経済的にも安全面においても好ましくない。 As a method for promoting the stabilization of fat and oil crystals, a method for obtaining fine and stable crystals in a short time by rapidly pressing up to 10 to 50 MPa at a pressing speed of 5 MPa / second or more immediately before crystallization of fats and oils (patent) Reference 5) and a method of accelerating or stabilizing oil and fat crystallization by performing pulsed magnetic field treatment in the oil and fat crystallization process (Patent Document 6) have been proposed. This requires an apparatus that performs a stable pulse magnetic field, which is not preferable in terms of economy and safety.

特公平4−58941号公報Japanese Patent Publication No. 4-58941 特公平6−95879号公報Japanese Examined Patent Publication No. 6-95879 特公平7−108185号公報Japanese Examined Patent Publication No. 7-108185 特許第2733286号公報Japanese Patent No. 2733286 特開2001−321080号公報JP 2001-321080 A 特開2005−312416号公報JP 2005-31416 A

このように、チョコレート添加剤に必要な、油脂の安定型結晶を得るためには、温調による長時間の結晶転移工程や特殊な装置を利用しなければならず、安定結晶転移工程の簡便化による製造コストの低減が望まれていた。 Thus, in order to obtain the stable crystals of fats and oils necessary for chocolate additives, it is necessary to use a long-time crystal transition process by temperature control and special equipment, simplifying the stable crystal transition process Therefore, it has been desired to reduce the manufacturing cost.

本発明者らは、前記課題を解決するため鋭意研究を重ねた結果、SUS型トリグリセリド(Sは炭素数16〜24の飽和脂肪酸残基、Uは炭素数18以上の不飽和脂肪酸残基)に炭素数4〜12の飽和脂肪酸を含む油脂を配合することにより、安定型結晶への転移が常温、短時間で完了するという知見を見出し、本発明を完成するに至った。 As a result of intensive studies to solve the above problems, the present inventors have found that SUS-type triglycerides (S is a saturated fatty acid residue having 16 to 24 carbon atoms, U is an unsaturated fatty acid residue having 18 or more carbon atoms). By blending fats and oils containing saturated fatty acids having 4 to 12 carbon atoms, the inventors have found that the transition to stable crystals can be completed in a short time at room temperature, and have completed the present invention.

即ち、本発明の第一は、炭素数4〜12の飽和脂肪酸を50重量%以上含む油脂(油脂A)とSUS型トリグリセリド(Sは炭素数16〜24の飽和脂肪酸残基、Uは炭素数18以上の不飽和脂肪酸残基)を含有するチョコレート添加剤である。第二は、SUS型トリグリセリドが1,3−ジベヘノイル−2−オレイルグリセリドである第一記載のチョコレート添加剤である。第三は、油脂Aが炭素数4〜12の飽和脂肪酸を75重量%以上含む油脂である第一記載のチョコレート添加剤である。第四は、油脂Aが炭素数4〜10の飽和脂肪酸を75重量%以上含む油脂である第三記載のチョコレート添加剤である。第五は、油脂Aが炭素数4〜10の飽和脂肪酸からなるトリ飽和グリセリドである第四記載のチョコレート添加剤である。第六は、(油脂A)/(SUS型トリグリセリド)が重量比率で0.2〜3である第一記載のチョコレート添加剤である。第七は、油脂A及びSUS型トリグリセリドを融解混合し、結晶化させることを特徴とする第一〜六いずれか記載のチョコレート添加剤の製造方法である。第八は、第一〜六いずれか記載のチョコレート添加剤をチョコレート生地の冷却過程で添加することを特徴とするチョコレートの製造方法である。 That is, the first of the present invention is an oil (oil A) containing 50% by weight or more of a saturated fatty acid having 4 to 12 carbon atoms and an SUS triglyceride (S is a saturated fatty acid residue having 16 to 24 carbon atoms, U is a carbon number. It is a chocolate additive containing 18 or more unsaturated fatty acid residues). The second is the chocolate additive as described in the first item, wherein the SUS type triglyceride is 1,3-dibenoyl-2-oleyl glyceride. 3rd is a chocolate additive of 1st description whose fats and oils are fats and oils containing 75 weight% or more of C4-C12 saturated fatty acids. 4th is a chocolate additive of the 3rd description whose fats and oils are fats and oils containing 75 weight% or more of C4-C10 saturated fatty acids. The fifth is the chocolate additive according to the fourth, wherein the fat A is a trisaturated glyceride composed of a saturated fatty acid having 4 to 10 carbon atoms. Sixth is the chocolate additive according to the first aspect, wherein (fat A) / (SUS type triglyceride) is 0.2 to 3 by weight ratio. 7th is the manufacturing method of the chocolate additive in any one of the 1st-6th characterized by melt-mixing fats and oils A and SUS type | mold triglyceride, and making it crystallize. Eighth is a method for producing chocolate, wherein the chocolate additive according to any one of the first to sixth is added during the cooling process of the chocolate dough.

本発明におけるチョコレート添加剤は、従来のチョコレート添加剤に必須であった油脂の安定型結晶粉末を別途調製し添加する工程が必要なく、また、従来油脂を安定型結晶に転移させるために必須であった、高温かつ長時間の結晶転移工程を必要としないため、常温、短時間で安定型結晶への転移を完了させることができ、製造工程の短縮化、製造コストの低減に大きく寄与する。さらに、得られたチョコレート添加剤は、ペースト状であるため、チョコレートへの分散性がよく、テンパリング作業の効率化をも図ることが出来る。 The chocolate additive in the present invention does not require a step of separately preparing and adding a stable crystal powder of oils and fats, which was essential for conventional chocolate additives, and is essential for transferring conventional fats and oils to stable crystals. Since there is no need for a high-temperature and long-time crystal transition step, the transition to a stable crystal can be completed at room temperature and in a short time, which greatly contributes to shortening the manufacturing process and reducing manufacturing costs. Furthermore, since the obtained chocolate additive is paste-like, the dispersibility to chocolate is good and the tempering work can be made more efficient.

以下、本発明をより詳細に説明する。 Hereinafter, the present invention will be described in more detail.

本発明におけるチョコレート添加剤に含有する、SUS型トリグリセリドとは、Sは炭素数16〜24の飽和脂肪酸残基、Uは炭素数18以上の不飽和脂肪酸残基からなる1、3−ジ飽和―2−不飽和グリセリドのことを表し、上記飽和脂肪酸Sとしては、パルミチン酸、ステアリン酸、アラキジン酸、ベヘン酸などがあり、上記不飽和脂肪酸Uとしては、オレイン酸、リノール酸などが挙げられ、上記脂肪酸を含むSUS型トリグリセリドとして、1,3−ジステアロイル−2−オレイルグリセリド、1−ステアロイル−2−オレイル−3−パルミトイルグリセリド、1,3−ジパルミトイル−2−オレイルグリセリドを含むココアバター、ココアバター代用脂、ココアバター改質脂などを挙げることができる。 The SUS-type triglyceride contained in the chocolate additive in the present invention is that S is a saturated fatty acid residue having 16 to 24 carbon atoms, and U is a 1,3-di-saturated residue consisting of an unsaturated fatty acid residue having 18 or more carbon atoms. 2- represents an unsaturated glyceride, and the saturated fatty acid S includes palmitic acid, stearic acid, arachidic acid, behenic acid, etc., and the unsaturated fatty acid U includes oleic acid, linoleic acid, etc. As SUS type triglyceride containing the fatty acid, cocoa butter containing 1,3-distearoyl-2-oleyl glyceride, 1-stearoyl-2-oleyl-3-palmitoyl glyceride, 1,3-dipalmitoyl-2-oleyl glyceride, Examples include cocoa butter substitute fat and cocoa butter modified fat.

本発明におけるチョコレート添加剤は、ファットブルーム抑制効果として、比較的高温のブルームに耐える性質のため、或いは、体温を超えるような高温に曝された後に艶のあるチョコレートに復帰する機能を期待するにはSUS型トリグリセリドが1,3−ジベヘノイル−2−オレイルグリセリドであることがより好ましい。 The chocolate additive in the present invention is expected to have a function to return to glossy chocolate after being exposed to a high temperature exceeding the body temperature because of its ability to withstand a relatively high temperature bloom as a fat bloom suppressing effect. More preferably, the SUS type triglyceride is 1,3-dibehenoyl-2-oleyl glyceride.

本発明におけるチョコレート添加剤は、炭素数4〜12の飽和脂肪酸を50重量%以上含む油脂(油脂A)を上記SUS型トリグリセリドと混合することにより、SUS型トリグリセリドの安定型結晶への転移を短縮することが可能とするものであり、炭素数が4未満の飽和脂肪酸や炭素数が12を超える飽和脂肪酸あるいは炭素数4〜12の飽和脂肪酸を50重量%未満しか含まない油脂では、SUS型トリグリセリドの安定型結晶への転移を促進する効果は得られない。炭素数4〜12の飽和脂肪酸を50重量%以上含む油脂としては、パーム核油、ヤシ油、乳脂等のラウリン酸、及び中短鎖脂肪酸を含む油脂の分別軟質部等が挙げられる。 The chocolate additive in the present invention shortens the transition of SUS triglycerides to stable crystals by mixing fat (oil A) containing 50% by weight or more of saturated fatty acids having 4 to 12 carbon atoms with the SUS triglyceride. SUS-type triglycerides for fats and oils containing less than 50% by weight of saturated fatty acids having less than 4 carbon atoms, saturated fatty acids having more than 12 carbon atoms, or saturated fatty acids having 4 to 12 carbon atoms. The effect of promoting the transition to a stable crystal cannot be obtained. Examples of oils and fats containing 50% by weight or more of saturated fatty acids having 4 to 12 carbon atoms include lauric acid such as palm kernel oil, coconut oil and milk fat, and fractionated soft parts of fats and oils containing medium and short chain fatty acids.

また、本発明におけるチョコレート添加剤に含有する油脂Aは、炭素数4〜12の飽和脂肪酸を75重量%以上含む油脂、さらには炭素数4〜10の飽和脂肪酸を75重量%以上含む油脂であることが好ましい。炭素数4〜12の飽和脂肪酸を75重量%以上含む油脂としては、パーム核油、ヤシ油、乳脂等のラウリン酸、及び中短鎖脂肪酸を含む油脂の分別軟質部、あるいは炭素数4〜10の飽和脂肪酸からなるトリ飽和グリセリドの少なくとも1種と液状油脂との金属エステル交換油、酵素エステル交換油等が挙げられる。 Moreover, the fats and oils A contained in the chocolate additive in the present invention are fats and oils containing 75 wt% or more of saturated fatty acids having 4 to 12 carbon atoms, and further fats and oils containing 75 wt% or more of saturated fatty acids having 4 to 10 carbon atoms. It is preferable. As fats and oils containing 75 wt% or more of saturated fatty acids having 4 to 12 carbon atoms, fractionated soft parts of fats and oils containing lauric acids such as palm kernel oil, coconut oil and milk fat, and medium and short chain fatty acids, or carbon numbers of 4 to 10 Metal transesterification oil, enzyme transesterification oil, etc. of at least 1 sort of trisaturated glyceride which consists of these saturated fatty acids, and liquid fats and oils are mentioned.

さらに、本発明におけるチョコレート添加剤に含有する油脂Aは、炭素数4〜10の飽和脂肪酸からなるトリ飽和グリセリドであることが最も好ましく、これによりSUS型トリグリセリドの安定型結晶への転移をより短縮させることが可能となる。 Further, the fat A contained in the chocolate additive in the present invention is most preferably a trisaturated glyceride composed of a saturated fatty acid having 4 to 10 carbon atoms, thereby further shortening the transition of SUS type triglycerides to stable crystals. It becomes possible to make it.

さらに本発明におけるチョコレート添加剤は、(油脂A)/(SUS型トリグリセリド)が重量比率で0.2〜3の範囲にあることが好ましく、より好ましくは0.3〜2である。SUS型トリグリセリドに対する油脂Aの重量比率が低すぎると、安定化促進効果が弱く、高すぎる場合は、シード機能を発揮させるために本発明のチョコレート添加剤の添加量を極端に増やす必要があり、結果的にチョコレート油分が高くなり、チョコレートの硬さが低下してしまうため好ましくない。 Furthermore, as for the chocolate additive in this invention, it is preferable that (oil fat A) / (SUS type triglyceride) exists in the range of 0.2-3 by weight ratio, More preferably, it is 0.3-2. If the weight ratio of the fat A to the SUS type triglyceride is too low, the stabilization promoting effect is weak, and if it is too high, it is necessary to extremely increase the amount of the chocolate additive of the present invention to exert the seed function, As a result, the chocolate oil content becomes high and the hardness of the chocolate is lowered, which is not preferable.

本発明におけるチョコレート添加剤は、上記SUS型トリグリセリド及び油脂Aの他に任意の油脂を配合することで、チョコレート添加剤の物性を任意に調整することができるが、油脂としては、液状油であることが好ましく、ヒマワリ油、菜種油、大豆油、米糠油、及びこれらの混合油、金属エステル交換油、酵素エステル交換油などを例示することができ、これら液状油と油脂Aの金属エステル交換油、酵素エステル交換油をSUS型トリグリセリドと配合しても良い。 The chocolate additive in the present invention can arbitrarily adjust the physical properties of the chocolate additive by blending any of the above SUS type triglycerides and fats and oils A, but the fats and oils are liquid oils. Preferably, sunflower oil, rapeseed oil, soybean oil, rice bran oil, and mixed oils thereof, metal transesterified oil, enzyme transesterified oil, and the like can be exemplified, and these liquid oil and metal transesterified oil of fat A, Enzyme transesterified oil may be blended with SUS-type triglycerides.

本発明におけるチョコレート添加剤の製造方法は、SUS型トリグリセリドと炭素数4〜12の飽和脂肪酸を50重量%以上含む油脂Aの混合物を融解状態で容器中に充填(例えばピロー包装)し、これを常温付近の温度に冷却して油脂結晶を析出せしめ、SUS型トリグリセリドの結晶を安定型へ転移させることで添加剤を得ることができる。安定型へ転移させるために、チョコレート添加剤が完全に固化しない程度の20℃付近の温度域で、数日間保存しておくだけでも転移させることができるが、25〜50℃、より好ましくは30〜40℃に温調することにより、安定型への転移をより促進させる事ができ好ましい。その際、25〜50℃にて温調する時間は24時間程度あればよく、従来、安定型への転移に必要であった温度や時間と比較すると大幅に結晶転移工程を短縮、簡略化することが可能である。 The manufacturing method of the chocolate additive in this invention fills the container of the fats and oils A containing 50 weight% or more of SUS type triglycerides and a C4-C12 saturated fatty acid in a molten state (for example, pillow wrapping), The additive can be obtained by cooling to a temperature near room temperature to precipitate oil and fat crystals and transferring the crystals of SUS triglyceride to a stable type. In order to make it transfer to a stable type, it can be transferred even if it is stored for several days in a temperature range around 20 ° C. where the chocolate additive is not completely solidified, but it is 25-50 ° C., more preferably 30 ° C. By controlling the temperature to ˜40 ° C., the transition to the stable type can be further promoted, which is preferable. At that time, the temperature adjustment time at 25 to 50 ° C. may be about 24 hours, which greatly shortens and simplifies the crystal transition process compared with the temperature and time conventionally required for the transition to the stable type. It is possible.

本発明におけるチョコレート添加剤のSUS型トリグリセリドの安定型結晶とは、X線回折スペクトルで短面間隔(側面間隔)のピークが4本以上あらわれる結晶型であり、好ましくは、R.L.WilleおよびE.S.Luttonがココアバターの結晶型について命名している方法[J.A.O.C.S.,43,491−496(1966)]での、V型以上の安定な結晶型、およびT.Koyano等が1,3−ジステアロイル−2−オレイルグリセリド、1,3−ジパルミトイル−2−オレイルグリセリドの結晶型に使用しているβ2以上の安定な結晶型[J.O.C.S.,66,no5,664−674(1989)]をいう。 The stable crystal of the SUS type triglyceride as the chocolate additive in the present invention is a crystal type in which four or more short face interval (side surface interval) peaks appear in the X-ray diffraction spectrum. L. Wille and E.W. S. The method Luton names for the crystalline form of cocoa butter [J. A. O. C. S. , 43, 491-496 (1966)], a stable crystal form of V type or higher, and T. Koyano et al. Uses a stable crystal form of β2 or higher, which is used for crystal forms of 1,3-distearoyl-2-oleylglyceride and 1,3-dipalmitoyl-2-oleylglyceride [J. O. C. S. , 66, no 5, 664-674 (1989)].

上記製造方法により得られた、本発明のチョコレート添加剤は、ペースト状であるため、従来の粉末状のチョコレート添加剤と比較すると、粘性のあるチョコレートに添加する際に、容易に均一に分散させることが出来、チョコレート製造工程において、テンパリング作業の効率化を図ることができるという効果も有する。 The chocolate additive of the present invention obtained by the above production method is in a paste form, so that it is easily and uniformly dispersed when added to viscous chocolate as compared with a conventional powdered chocolate additive. It is also possible to improve the efficiency of the tempering work in the chocolate manufacturing process.

本発明におけるチョコレート添加剤は、チョコレートの原料油脂として、ココアバターや、ココアバターに代用して使用されるハードバターを使用したいわゆるテンパリング型チョコレート類に好ましく適用でき、チョコレート類への本発明のチョコレート添加剤の添加量としては0.1〜10重量%が好ましい。また、本発明のチョコレート添加剤のチョコレート類への添加方法としては、チョコレート生地の冷却工程において、品温27〜37℃で添加することが好ましく、当該添加後、チョコレート生地はリヒートなしに成型又はエンロービングすることができる。かかる使用方法は従来のシーディング法と呼ばれる方法に準じて実施することができる。 The chocolate additive in the present invention is preferably applicable to so-called tempering chocolates using cocoa butter or hard butter used in place of cocoa butter as a raw material fat of chocolate, and the chocolate of the present invention to chocolates The addition amount of the additive is preferably 0.1 to 10% by weight. Moreover, as a method for adding the chocolate additive of the present invention to chocolates, it is preferable to add at a product temperature of 27 to 37 ° C. in the chocolate dough cooling step, and after the addition, the chocolate dough is molded or reheated without reheating. Can be enrobed. Such a method of use can be carried out according to a method called a conventional seeding method.

以下に本発明の実施例を示し、本発明をより詳細に説明する。なお、例中、%および部はいずれも重量基準を意味する。 Examples of the present invention will be described below to explain the present invention in more detail. In the examples, “%” and “part” mean weight basis.

(1、3−ジステアロイル−2−オレイルグリセリド含有油脂の調製)
オレイン酸エチルエステルと高オレイン酸ヒマワリ油とを用い、1−、3−位選択性を有する酵素剤にて既知の方法によりエステル交換反応を行い、さらに溶剤分別により高融点画分を分取した。この画分には64.5%の1、3−ジステアロイル−2−オレイルグリセリド(StOSt)が含まれており、SUS型トリグリセリドの合計は85.2%であった。これをStOSt脂とした。
(Preparation of fat containing 1,3-distearoyl-2-oleylglyceride)
Using oleic acid ethyl ester and high oleic sunflower oil, transesterification was carried out by a known method with an enzyme agent having 1-, 3-position selectivity, and a high melting point fraction was fractionated by solvent fractionation. . This fraction contained 64.5% of 1,3-distearoyl-2-oleyl glyceride (StOSt), and the total of SUS type triglycerides was 85.2%. This was designated as StOSt fat.

(1、3−ジベヘノイル−2−オレイルグリセリド含有油脂の調製)
高エルシン酸菜種油の極度硬化油を加水分解して得た脂肪酸またはその低級アルコールエステルとエステル交換し、さらには精溜することにより得られる炭素数20〜24個が豊富である飽和脂肪酸エステルと高オレイン酸ヒマワリ油とを用い、1−、3−位選択性を有する酵素剤にて既知の方法によりエステル交換反応を行い、さらに溶剤分別により高融点画分を分取した。この画分には、68.0%の1、3−ジベヘノイル−2−オレイルグリセリド(BOB)が含まれており、SUS型トリグリセリドの合計は84.4%であった。これをBOB脂とした。
(Preparation of fat containing 1,3-dibehenoyl-2-oleylglyceride)
Saturated fatty acid ester rich in 20 to 24 carbon atoms obtained by transesterification with fatty acid obtained by hydrolyzing extremely hardened oil of high erucic acid rapeseed oil or its lower alcohol ester, and further by rectification Using oleic sunflower oil, a transesterification reaction was performed by a known method using an enzyme agent having 1- and 3-position selectivity, and a high melting point fraction was further fractionated by solvent fractionation. This fraction contained 68.0% 1,3-dibehenoyl-2-oleyl glyceride (BOB), and the total of SUS type triglycerides was 84.4%. This was designated as BOB fat.

(実施例1)
油脂Aとして精製パーム核分別軟質部(脂肪酸組成:炭素数6含量1.1%、炭素数8含量9.5%、炭素数10含量4.6% 炭素数12含量38.4% 炭素数14含量10.1% 炭素数16含量7.7% 炭素数18含量2.1% 炭素数18:1含量23.1% 炭素数18:2含量3.4%)50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が32℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
Example 1
Refined palm core fraction soft part as fat and oil A (fatty acid composition: carbon number 6 content 1.1%, carbon number 8 content 9.5%, carbon number 10 content 4.6%, carbon number 12 content 38.4%, carbon number 14 Content 10.1% carbon number 16 content 7.7% carbon number 18 content 2.1% carbon number 18: 1 content 23.1% carbon number 18: 2 content 3.4%) and 50 parts BOB fat Mixing was performed in a molten state, and after complete melting and mixing at 70 ° C., the product was cooled in a water bath at a water temperature of 15 ° C. until the product temperature of the oil and fat was 32 ° C. to precipitate crystals. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例2)
実施例1の精製パーム核分別軟質部50部と「スコレー8」(日清オイリオグループ社製、脂肪酸組成:炭素数8含量99.9%、炭素数10含量0.1%)50部を混合し、常法によりナトリウムメチラートを用い金属エステル交換を行った後、脱色、脱臭して得られた油脂を油脂Aとした。この油脂Aの炭素数4〜12の飽和脂肪酸含量は76.8%であった。この油脂A50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が32℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 2)
50 parts of the purified palm core fractionation soft part of Example 1 and 50 parts of “Scoray 8” (manufactured by Nisshin Oilio Group, fatty acid composition: carbon number 8 content 99.9%, carbon number 10 content 0.1%) The oil and fat obtained by decolorization and deodorization after performing metal transesterification using sodium methylate by a conventional method was designated as fat and oil A. The fat and oil A had a saturated fatty acid content of 4 to 12 carbon atoms of 76.8%. 50 parts of this fat and oil and 50 parts of BOB fat were mixed in a molten state, and after complete melting and mixing at 70 ° C., cooling was performed until the product temperature of the fat was 32 ° C. in a water bath at a water temperature of 15 ° C. to precipitate crystals. . This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例3)
実施例2で使用した「スコレー8」80部とハイオレイックヒマワリ油(脂肪酸組成:炭素数16含量3.8% 炭素数18含量4.2% 炭素数20含量0.5% 炭素数18:1含量79.7% 炭素数18:2含量10.4% 炭素数18:3含量0.4% 炭素数22:1含量1.0%)20部を混合し、常法によりナトリウムメチラートを用い金属エステル交換を行った後、脱色、脱臭して得られた油脂を油脂Aとした。この油脂Aの炭素数4〜10の飽和脂肪酸含量は79.9%であった。この油脂A50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が32℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 3)
80 parts of “Skoray 8” used in Example 2 and high oleic sunflower oil (fatty acid composition: carbon number 16 content 3.8% carbon number 18 content 4.2% carbon number 20 content 0.5% carbon number 18: 1 content 79.7% carbon number 18: 2 content 10.4% carbon number 18: 3 content 0.4% carbon number 22: 1 content 1.0%) 20 parts are mixed and sodium methylate is added by a conventional method. After the transesterification was performed, the oil and fat obtained by decolorization and deodorization was designated as oil A. The content of saturated fatty acids having 4 to 10 carbon atoms of the fat A was 79.9%. 50 parts of this fat and oil and 50 parts of BOB fat were mixed in a molten state, and after complete melting and mixing at 70 ° C., cooling was performed until the product temperature of the fat was 32 ° C. in a water bath at a water temperature of 15 ° C. to precipitate crystals. . This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例4)
油脂Aとして実施例2で使用した「スコレー8」25部とBOB脂50部及びStOSt脂25部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が32℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 4)
25 parts of “Skoray 8” used in Example 2 as fats and oils A, 50 parts of BOB fats and 25 parts of StOSt fats were mixed in a molten state, and after complete melting and mixing at 70 ° C., the fats and oils were mixed in a water bath at a water temperature of 15 ° C. Crystals were precipitated by cooling until the product temperature reached 32 ° C. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例5)
油脂AとしてMCT−B(不二製油株式会社製、脂肪酸組成:炭素数8含量55.1%、炭素数10含量44.2%、炭素数14含量0.7%)25部とBOB脂75部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が38℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、45℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温45℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温45℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 5)
Fat and oil A as MCT-B (Fuji Oil Co., Ltd., fatty acid composition: carbon number 8 content 55.1%, carbon number 10 content 44.2%, carbon number 14 content 0.7%) and BOB fat 75 Parts were mixed in a molten state, and after complete melting and mixing at 70 ° C., cooling was performed until the product temperature of the oil and fat reached 38 ° C. in a water bath having a water temperature of 15 ° C. to precipitate crystals. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 45 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a temperature of 45 ° C was added to 97 parts of chocolate kept at 33 ° C after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 45 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例6)
油脂Aとして「スコレー8」25部とBOB脂50部、および実施例3で使用したハイオレイックヒマワリ油25部を融解状態で混合し、70℃にて完全融解の後、水温15℃の水槽中で油脂の品温が33℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 6)
As oil / fat A, 25 parts of “Skoray 8”, 50 parts of BOB fat and 25 parts of high oleic sunflower oil used in Example 3 were mixed in a melted state, completely melted at 70 ° C., and a water bath at a water temperature of 15 ° C. The crystals were precipitated by cooling until the product temperature of the oil and fat reached 33 ° C. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例7)
油脂AとしてMCT−B50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が33℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 7)
50 parts of MCT-B and 50 parts of BOB fat are mixed in a melted state as fat and oil A. After complete melt mixing at 70 ° C, the crystals are cooled in a water bath at a water temperature of 15 ° C until the product temperature of the fat and oil reaches 33 ° C. Precipitated. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例8)
油脂Aとして「スコレー8」50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が33℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 8)
As fat and oil A, 50 parts of “Skolay 8” and 50 parts of BOB fat are mixed in a melted state. Crystals were precipitated. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例9)
油脂Aとしてトリブチリン(Sigma−Aldrich社製、脂肪酸組成:炭素数4含量100%)50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が36℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
Example 9
As fat / oil A, 50 parts of tributyrin (manufactured by Sigma-Aldrich, fatty acid composition: carbon number 4 content 100%) and 50 parts of BOB fat were mixed in a melted state, completely melted and mixed at 70 ° C., and then in a water bath at 15 ° C. The oil and fat were cooled until the product temperature reached 36 ° C. to precipitate crystals. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例10)
油脂AとしてMCT−B65部とBOB脂35部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が31℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温40℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 10)
65 parts of MCT-B and 35 parts of BOB fat are mixed in a melted state as fat and oil A. After complete melt mixing at 70 ° C, the crystals are cooled in a water bath at a water temperature of 15 ° C until the product temperature of the fat and oil reaches 31 ° C. Precipitated. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 40 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例11)
油脂AとしてMCT−B65部とBOB脂35部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が31℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で8日間保存した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温20℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温20℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 11)
65 parts of MCT-B and 35 parts of BOB fat are mixed in a melted state as fat and oil A. After complete melt mixing at 70 ° C, the crystals are cooled in a water bath at a water temperature of 15 ° C until the product temperature of the fat and oil reaches 31 ° C. Precipitated. This was filled into a pillow and stored at 20 ° C. for 8 days. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive with a product temperature of 20 ° C was added to 97 parts of chocolate kept at 33 ° C after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 20 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(実施例12)
油脂AとしてMCT−B75部とBOB脂25部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が29℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、30℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2に転移していた。この品温30℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。尚、この品温30℃のチョコレート添加剤はペースト状であり、チョコレートに簡単に混合分散が可能であった。
(Example 12)
As fat and oil A, 75 parts of MCT-B and 25 parts of BOB fat are mixed in a melted state, completely melted and mixed at 70 ° C., and then cooled in a water bath at a water temperature of 15 ° C. until the product temperature of the fat and oil reaches 29 ° C. Precipitated. This was filled in a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 30 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was transferred to stable β2. 3 parts of this chocolate additive having a temperature of 30 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. There was no bloom and the seed function was good. The chocolate additive having a product temperature of 30 ° C. was pasty and could be easily mixed and dispersed in chocolate.

(比較例1)
BOB脂を70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が40℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、45℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、不安定型のp−β’であり、安定型のβ2には転移しなかった。
この品温45℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームが発生し、シード機能は無かった。また、45℃の添加剤は硬く、チョコレートに混合分散し難い状態であった。
(Comparative Example 1)
The BOB fat was completely melted and mixed at 70 ° C., and then cooled in a water bath at a water temperature of 15 ° C. until the product temperature of the fat became 40 ° C. to precipitate crystals. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 45 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was unstable p-β ′ and did not transfer to stable β2.
3 parts of this chocolate additive having a temperature of 45 ° C was added to 97 parts of chocolate kept at 33 ° C after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C for 30 minutes, and demolded. Bloom occurred and there was no seed function. The additive at 45 ° C. was hard and difficult to be mixed and dispersed in chocolate.

(比較例2)
比較例1と同様に、BOB脂を70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が40℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、45℃で静置し、経時的にX線回析を測定した結果、14日目でβ2に転移が認められた。この品温45℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームの発生は無くシード機能は良好であった。しかし、45℃の添加剤は硬く、チョコレートに混合分散し難い状態であった。
(Comparative Example 2)
In the same manner as in Comparative Example 1, BOB fat was completely melted and mixed at 70 ° C., and then cooled in a water bath at a water temperature of 15 ° C. until the product temperature of the oil and fat reached 40 ° C. to precipitate crystals. This was filled in a pillow, stored at 20 ° C. for 24 hours, allowed to stand at 45 ° C., and measured for X-ray diffraction over time. As a result, metastasis to β2 was observed on the 14th day. 3 parts of this chocolate additive having a temperature of 45 ° C was added to 97 parts of chocolate kept at 33 ° C after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C for 30 minutes, and demolded. There was no bloom and the seed function was good. However, the additive at 45 ° C. was hard and difficult to be mixed and dispersed in chocolate.

(比較例3)
油脂Aとしてトリアセチン(東京化成工業株式会社製、脂肪酸組成:炭素数2含量100%)50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が36℃になるまで冷却して結晶を析出させた。しかし、固液分離が起こり、均一なペースト状にはならなかった。また、固液分離した結晶部分だけをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、不安定型のp−β’であり、安定型のβ2には転移しなかった。この品温40℃のチョコレート添加剤3部、を完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームが発生しシード機能は無かった。また、40℃の添加剤は硬く、チョコレートに混合分散し難い状態であった。
(Comparative Example 3)
As fat and oil A, 50 parts of triacetin (manufactured by Tokyo Chemical Industry Co., Ltd., fatty acid composition: 2 carbon content: 100%) and 50 parts of BOB fat are mixed in a melted state, completely melted and mixed at 70 ° C, and then a water bath with a water temperature of 15 ° C. The crystals were precipitated by cooling until the product temperature of the oil and fat reached 36 ° C. However, solid-liquid separation occurred and did not become a uniform paste. Further, only the crystal part separated by solid-liquid separation was filled in a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring the X-ray diffraction of this chocolate additive, it was unstable p-β ′ and did not transfer to stable β2. 3 parts of this chocolate additive having a temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after being completely melted, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and then demolded. Bloom occurred and there was no seed function. Further, the additive at 40 ° C. was hard and difficult to be mixed and dispersed in chocolate.

(比較例4)
実施例3で使用したハイオレイックヒマワリ油50部とBOB脂50部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が33℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃で24時間静置した。このチョコレート添加剤のX線回析を測定した結果、安定型のβ2のピークも認められたが、不安定型のp−β’のピークがメインピークであった。この品温40℃のチョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームが発生し、シード機能は無かった。尚、この品温40℃のチョコレート添加剤はペースト状ではあるが、やや硬く、チョコレートへやや混合分散し難い状態であった。
(Comparative Example 4)
50 parts of high oleic sunflower oil used in Example 3 and 50 parts of BOB fat were mixed in a molten state, and after complete melting and mixing at 70 ° C, the product temperature of the oil and fat was 33 ° C in a water bath at a water temperature of 15 ° C. Crystals were precipitated by cooling. This was filled into a pillow, stored at 20 ° C. for 24 hours, and then allowed to stand at 40 ° C. for 24 hours. As a result of measuring X-ray diffraction of this chocolate additive, a stable β2 peak was also observed, but an unstable p-β ′ peak was the main peak. 3 parts of this chocolate additive having a product temperature of 40 ° C. was added to 97 parts of chocolate kept at 33 ° C. after complete melting, mixed, poured into a mold without reheating, solidified by cooling at 5 ° C. for 30 minutes, and demolded. Bloom occurred and there was no seed function. Although the chocolate additive having a product temperature of 40 ° C. is in a paste form, it is a little hard and slightly mixed and dispersed in the chocolate.

(比較例5)
油脂AとしてMCT−B10部とBOB脂90部を融解状態で混合し、70℃にて完全融解混合後、水温15℃の水槽中で油脂の品温が38℃になるまで冷却して結晶を析出させた。これをピローに充填し、20℃で24時間保存後、40℃、45℃、48℃の各温度でそれぞれ24時間静置した。この3種のチョコレート添加剤のX線回析を測定した結果、不安定型のp−β’であり、安定型のβ2には転移しなかった。また、各温度の添加剤は硬く、使用し難い状態であった。この品温40℃/45℃/48℃の各チョコレート添加剤3部を、完全融解後33℃に保温したチョコレート97部に添加、混合し、リヒート無しで、モールドに流し、5℃で30分間冷却固化後デモールドしたところ、ブルームが発生した。また、各添加剤はやや硬く、チョコレートにやや混合分散し難い状態であった。
(Comparative Example 5)
As fat and oil A, 10 parts of MCT-B and 90 parts of BOB fat are mixed in a melted state, completely melted and mixed at 70 ° C., and then cooled until the product temperature of the fat and oil reaches 38 ° C. Precipitated. This was filled in a pillow, stored at 20 ° C. for 24 hours, and allowed to stand at 40 ° C., 45 ° C., and 48 ° C. for 24 hours. As a result of measuring the X-ray diffraction of these three kinds of chocolate additives, it was unstable p-β ′ and did not transfer to stable β2. Moreover, the additive at each temperature was hard and difficult to use. 3 parts of each chocolate additive having a product temperature of 40 ° C./45° C./48° C. is added to 97 parts of chocolate kept at 33 ° C. after being completely melted, mixed, poured into a mold without reheating, and 30 minutes at 5 ° C. Blooming occurred when demolding after cooling and solidification. Moreover, each additive was a little hard and it was in the state which was a little hard to mix and disperse | distribute to chocolate.

(自動復帰能テスト)
実施例1〜12および比較例1〜5で得られたチョコレート添加剤を用いてテンパリングしたチョコレートを、20℃〜37℃/24時間1サイクルのサイクルテストに供した。
実施例及び比較例のチョコレート添加剤の評価、チョコレートテストの結果を表に示す。
(Automatic return ability test)
The chocolate tempered using the chocolate additive obtained in Examples 1 to 12 and Comparative Examples 1 to 5 was subjected to a cycle test of 20 ° C to 37 ° C / 24 hours for one cycle.
The evaluation of the chocolate additive of an Example and a comparative example and the result of a chocolate test are shown in a table | surface.

(表)

Figure 0005493862
*1 結晶型:○/β2安定型、×/p−β’不安定型
*2 分散性:○/良好、△/やや分散性悪い、×/分散しにくい
*3 シード機能評価:○/ブルーム発生なし、×/直後にブルーム発生
*4 自動復帰機能評価:○/5サイクル後もブルーム発生なし、△/3サイクル後にブルーム発生、×/1サイクル後にブルーム発生(table)
Figure 0005493862
* 1 Crystalline type: ○ / β2 stable type, × / p-β ′ unstable type * 2 Dispersibility: ○ / good, Δ / slightly dispersible, x / difficult to disperse * 3 Seed function evaluation: ○ / bloom generation None, bloom occurs immediately after × / * 4 Automatic recovery function evaluation: ○ No bloom occurs after 5 cycles, bloom occurs after Δ / 3 cycles, bloom occurs after × / 1 cycles

Claims (6)

炭素数4〜10の飽和脂肪酸を75重量%以上含む油脂(油脂A)とSUS型トリグリセリド(Sは炭素数16〜24の飽和脂肪酸残基、Uは炭素数18以上の不飽和脂肪酸残基)を含有するチョコレート添加剤。 Fats and oils (oil A) containing 75% by weight or more of saturated fatty acids having 4 to 10 carbon atoms and SUS triglycerides (S is a saturated fatty acid residue having 16 to 24 carbon atoms, U is an unsaturated fatty acid residue having 18 or more carbon atoms) Containing chocolate additives. SUS型トリグリセリドが1,3−ジベヘノイル−2−オレイルグリセリドである請求項1記載のチョコレート添加剤。 The chocolate additive according to claim 1, wherein the SUS type triglyceride is 1,3-dibehenoyl-2-oleyl glyceride. 油脂Aが炭素数4〜10の飽和脂肪酸からなるトリ飽和グリセリドである請求項記載のチョコレート添加剤。 Chocolate additive as claimed in claim 1 wherein the tri-saturated glycerides consisting of saturated fatty acids of the fat A is C4-10. (油脂A)/(SUS型トリグリセリド)が重量比率で0.2〜3である請求項1記載のチョコレート添加剤。 The chocolate additive according to claim 1, wherein (fat A) / (SUS type triglyceride) is 0.2 to 3 by weight ratio. 油脂A及びSUS型トリグリセリドを融解混合し、結晶化させることを特徴とする請求項1〜いずれか記載のチョコレート添加剤の製造方法。 Oil and fat A and SUS type triglyceride are melt-mixed and crystallized, The manufacturing method of the chocolate additive in any one of Claims 1-4 characterized by the above-mentioned. 請求項1〜いずれか記載のチョコレート添加剤をチョコレート生地の冷却過程で添加することを特徴とするチョコレートの製造方法。 A method for producing chocolate, comprising adding the chocolate additive according to any one of claims 1 to 4 during the cooling process of the chocolate dough.
JP2009540042A 2007-11-05 2008-11-04 Chocolate additive and method for producing the same Active JP5493862B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2009540042A JP5493862B2 (en) 2007-11-05 2008-11-04 Chocolate additive and method for producing the same

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2007286933 2007-11-05
JP2007286933 2007-11-05
JP2009540042A JP5493862B2 (en) 2007-11-05 2008-11-04 Chocolate additive and method for producing the same
PCT/JP2008/070001 WO2009060809A1 (en) 2007-11-05 2008-11-04 Chocolate additive and method of producing the same

Publications (2)

Publication Number Publication Date
JPWO2009060809A1 JPWO2009060809A1 (en) 2011-03-24
JP5493862B2 true JP5493862B2 (en) 2014-05-14

Family

ID=40625700

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009540042A Active JP5493862B2 (en) 2007-11-05 2008-11-04 Chocolate additive and method for producing the same

Country Status (2)

Country Link
JP (1) JP5493862B2 (en)
WO (1) WO2009060809A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020022411A1 (en) * 2018-07-25 2020-01-30 株式会社明治 Additive for chocolate and chocolate containing same

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2851414A4 (en) * 2012-05-18 2016-01-13 J Oil Mills Inc Crystallization accelerator
EP2868204B1 (en) * 2012-06-27 2019-08-28 The Nisshin OilliO Group, Ltd. Method for producing chocolate-covered food product coated by the same, and method for preventing increase in viscosity of chocolate for coating
JP6668295B2 (en) * 2017-07-14 2020-03-18 日清オイリオグループ株式会社 Production method of fats and oils

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06292510A (en) * 1991-07-03 1994-10-21 Unilever Nv Improved chocolate composition
JPH0889173A (en) * 1994-09-27 1996-04-09 Meiji Seika Kaisha Ltd New chocolate
JPH09121771A (en) * 1995-11-02 1997-05-13 Lotte Co Ltd Palatability improver for chocolate and chocolate composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07108185B2 (en) * 1987-12-14 1995-11-22 不二製油株式会社 Chocolate shortening and chocolate manufacturing method
JPH1198952A (en) * 1997-09-29 1999-04-13 Fuji Oil Co Ltd Food containing oil and fat and its production
JP2007267716A (en) * 2006-03-31 2007-10-18 Fuji Oil Co Ltd Chocolate additive, method for producing the same, and method for producing chocolate
JP2008206490A (en) * 2007-02-28 2008-09-11 Fuji Oil Co Ltd Chocolate additive

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06292510A (en) * 1991-07-03 1994-10-21 Unilever Nv Improved chocolate composition
JPH0889173A (en) * 1994-09-27 1996-04-09 Meiji Seika Kaisha Ltd New chocolate
JPH09121771A (en) * 1995-11-02 1997-05-13 Lotte Co Ltd Palatability improver for chocolate and chocolate composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020022411A1 (en) * 2018-07-25 2020-01-30 株式会社明治 Additive for chocolate and chocolate containing same

Also Published As

Publication number Publication date
JPWO2009060809A1 (en) 2011-03-24
WO2009060809A1 (en) 2009-05-14

Similar Documents

Publication Publication Date Title
JP5998932B2 (en) Non-laurin, non-trans, non-tempering type confectionery fat and its production method
JP3491410B2 (en) Shortening and its use
EP0227364B1 (en) Hard butter composition
JP2008206490A (en) Chocolate additive
JP5980682B2 (en) Oil and fat composition and method for producing the same
JPH0121734B2 (en)
JPH07108185B2 (en) Chocolate shortening and chocolate manufacturing method
JP3327122B2 (en) Non-tempering hard butter
US5405639A (en) Non-tempering confectionary fat
JP5493862B2 (en) Chocolate additive and method for producing the same
WO2016125791A1 (en) Oil composition for chocolate and chocolate containing same
JP2008301731A (en) Oil and fat transition-resistant oil-and-fat composition
JP6103039B2 (en) Oil for preventing deterioration of texture and oil for chocolate comprising this
JP2016140313A (en) Fat composition for oily food and oily foods containing the same
JP2007259737A (en) Method for producing chocolate
JP3074832B2 (en) Chocolate production method
JP2733286B2 (en) Solidification aid for chocolates, chocolate containing the solidification aid, and method for producing the same
WO2013147279A1 (en) Non-tempered chocolate
JP6797851B2 (en) Chocolates and their manufacturing methods
JP2017079629A (en) Fat composition for chocolate, and chocolate containing the same
JP2020156415A (en) Bloom suppressing oil/fat composition and oily/fatty confectionery using the same
JP2019129796A (en) chocolate
JPH0588094B2 (en)
JP7006536B2 (en) Chocolates and their manufacturing methods
JP6044722B2 (en) Fatty food solidification accelerator

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20111018

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20130618

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130813

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20140204

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20140217

R150 Certificate of patent or registration of utility model

Ref document number: 5493862

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

S531 Written request for registration of change of domicile

Free format text: JAPANESE INTERMEDIATE CODE: R313531

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

S111 Request for change of ownership or part of ownership

Free format text: JAPANESE INTERMEDIATE CODE: R313111

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350