JP2008199950A - Packaged milk coffee beverage - Google Patents

Packaged milk coffee beverage Download PDF

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JP2008199950A
JP2008199950A JP2007039081A JP2007039081A JP2008199950A JP 2008199950 A JP2008199950 A JP 2008199950A JP 2007039081 A JP2007039081 A JP 2007039081A JP 2007039081 A JP2007039081 A JP 2007039081A JP 2008199950 A JP2008199950 A JP 2008199950A
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milk
coffee
coffee beverage
acid
milk coffee
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JP4012561B1 (en
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Shinji Yamamoto
真士 山本
Yoshinobu Hayakawa
義信 早川
Tatsuya Kusaura
達也 草浦
Hidefumi Yamane
英史 山根
Kiyoshi Kataoka
潔 片岡
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Kao Corp
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Kao Corp
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Priority to TW97105618A priority patent/TW200838436A/en
Priority to PCT/JP2008/053112 priority patent/WO2008102892A1/en
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    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23FCOFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
    • A23F5/00Coffee; Coffee substitutes; Preparations thereof
    • A23F5/24Extraction of coffee; Coffee extracts; Making instant coffee
    • A23F5/243Liquid, semi-liquid or non-dried semi-solid coffee extract preparations; Coffee gels; Liquid coffee in solid capsules

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
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  • Polymers & Plastics (AREA)
  • Tea And Coffee (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a packaged milk coffee beverage having high chlorogenic acid concentration, and excellent in stability and flavor in long-term preservation. <P>SOLUTION: The packaged milk coffee beverage is such that (A) a chlorogenic acid concentration is 0.14-0.5 mass%, (B) the mass ratio of chlorogenic acid to tannin is 0.6-0.97, (C) the mass ratio of dichlorogenic acid to chlorogenic acid is 0.06-0.13, and (D) the content of chinic acid is 0.021-0.2 g/100 g. The beverage is subjected to heat sterilization treatment. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

本発明は、クロロゲン酸濃度が高く、長期保存時の安定性及び風味に優れる流通販売を目的とした容器詰ミルクコーヒー飲料に関する。   The present invention relates to a packaged milk coffee beverage for the purpose of distribution and sales having a high chlorogenic acid concentration and excellent stability and flavor during long-term storage.

高血圧症の治療薬としては、神経因子による調節系に作用する各種神経遮断薬、液性因子に関わる調節系に作用するACE阻害薬、AT受容体拮抗薬、血管内皮由来物質による調節系に関わるCa拮抗薬、腎臓での体液調節系に関わる降圧利尿薬などの医薬品が挙げられ、これらは主として医療機関において、重症の高血圧患者に使用される。しかし、現状において高血圧症対策の目的で使用される医薬品は、有効性に関しては満足できる反面少なからず存在する副作用のため患者にかかる負担は大きい。   Antihypertensive drugs include various neuroleptic agents that act on the regulatory system of neural factors, ACE inhibitors that act on the regulatory system of humoral factors, AT receptor antagonists, and regulatory systems of vascular endothelium-derived substances Drugs such as Ca antagonists and antihypertensive diuretics related to the body fluid regulation system in the kidney can be mentioned, and these are mainly used in medical institutions for patients with severe hypertension. However, drugs currently used for the purpose of antihypertensive disease are satisfactory in terms of effectiveness, but the burden on patients is large due to the side effects that are present.

このため食事療法、運動療法、飲酒・喫煙の制限などの生活改善による一般療法が、軽症を含む正常高値高血圧症者から重症な高血圧症者に広く適用されている。一般療法の重要性の認識の高まりに伴い、特に食生活の改善が重要であるといわれ続けている。そして血圧降下作用を有する食品から食品由来の降圧素材の探索がさかんに行われ、その有効成分の分離・同定が数多く行われている。   For this reason, general therapies based on lifestyle improvements such as diet therapy, exercise therapy, restriction of drinking and smoking are widely applied to people with normal hypertension including mild to severe hypertension. With the increasing awareness of the importance of general therapy, it has been said that improving dietary habits is particularly important. Searches for food-derived antihypertensive materials from foods having an antihypertensive effect have been conducted extensively, and many active ingredients have been separated and identified.

一方、コーヒー飲料組成物内に含まれるヒドロキシヒドロキノンを低減させ、コーヒー飲料組成物中のヒドロキシヒドロキノン/クロロゲン酸類重量比率を10/10000以下にすることにより血圧降下作用が認められることが報告されている(特許文献1)。
また、クロロゲン酸濃度の高いものとしては、生豆抽出物を配合したものが提案されている(特許文献2,3)。
WO05/72533 特開2003−204755 特開2003−204756
On the other hand, it has been reported that the action of lowering blood pressure is recognized by reducing the hydroxyhydroquinone contained in the coffee beverage composition and setting the weight ratio of hydroxyhydroquinone / chlorogenic acids in the coffee beverage composition to 10 / 10,000 or less. (Patent Document 1).
Moreover, what mix | blended the raw bean extract as a thing with a high chlorogenic acid density | concentration is proposed (patent documents 2, 3).
WO05 / 72533 JP 2003-204755 A JP 2003-204756 A

本発明の目的は、クロロゲン酸濃度が高く、長期保存時の安定性及び風味に優れる流通販売を目的とした容器詰ミルクコーヒー飲料を提供することにある。   An object of the present invention is to provide a packaged milk coffee beverage having a high chlorogenic acid concentration and having the purpose of distribution and sales having excellent stability and flavor during long-term storage.

本発明者は、焙煎コーヒー豆特有の風味を維持しながら、長期保存時の安定性と風味に優れた容器詰ミルクコーヒー飲料について検討した結果、クロロゲン酸濃度、クロロゲン酸類/タンニン質量比率、並びにジクロロゲン酸類/クロロゲン酸類比率を特定範囲に制御することが極めて有効であることを見出した。   As a result of examining the containerized milk coffee beverage excellent in stability and flavor during long-term storage while maintaining the flavor unique to roasted coffee beans, the present inventor has found that the chlorogenic acid concentration, the chlorogenic acid / tannin mass ratio, and It has been found that it is extremely effective to control the dichlorogenic acid / chlorogenic acid ratio within a specific range.

すなわち、本発明は、
(A)クロロゲン酸類濃度0.14〜0.5質量%であり、
(B)クロロゲン酸類/タンニン0.6〜0.97質量比率であり、
(C)ジクロロゲン酸類/クロロゲン酸類0.06〜0.13質量比率であり、かつ、
(D)キナ酸の含有量が0.021〜0.2g/100gである
加熱殺菌処理を施した容器詰ミルクコーヒー飲料である。
That is, the present invention
(A) The chlorogenic acid concentration is 0.14-0.5% by mass,
(B) Chlorogenic acids / tannin 0.6 to 0.97 mass ratio,
(C) dichlorogenic acids / chlorogenic acids 0.06 to 0.13 mass ratio, and
(D) A container-packed milk coffee beverage subjected to a heat sterilization treatment in which the content of quinic acid is 0.021 to 0.2 g / 100 g.

本発明によれば、クロロゲン酸濃度が高く、長期保存時の安定性及び風味に優れた容器詰ミルクコーヒー飲料を得ることができる。   According to the present invention, it is possible to obtain a packaged milk coffee beverage having a high chlorogenic acid concentration and excellent stability and flavor during long-term storage.

本発明の容器詰ミルクコーヒー飲料は、生理効果及び風味、安定性の観点から、クロロゲン酸類を0.14〜0.5質量%(以下、特記しない限り単に%と言う)含有するが、好ましくは0.145〜0.4%、より好ましくは0.15〜0.37%、更に好ましくは0.155〜0.36%、特に好ましくは0.16〜0.2%含有する。当該クロロゲン酸類としては(A1)モノカフェオイルキナ酸、(A2)フェルラキナ酸、(A3)ジカフェオイルキナ酸の三種を含有する。ここで(A1)モノカフェオイルキナ酸としては3−カフェオイルキナ酸、4−カフェオイルキナ酸及び5−カフェオイルキナ酸から選ばれる1種以上が挙げられる。また(A2)フェルラキナ酸としては、3−フェルラキナ酸、4−フェルラキナ酸及び5−フェルラキナ酸から選ばれる1種以上が挙げられる。(A3)ジカフェオイルキナ酸としては3,4−ジカフェオイルキナ酸、3,5−ジカフェオイルキナ酸及び4,5−ジカフェオイルキナ酸から選ばれる1種以上が挙げられる。当該クロロゲン酸類の含有量は、高速液体クロマトグラフィー(HPLC)により測定することができる。HPLCにおける検出手段としては、UV検出で検出できる。更に、CL(化学発光)検出、EC(電気化学)検出、LC−Mass検出等によりクロロゲン酸類を高感度で検出することができる。
本発明では、ジクロロゲン酸類/クロロゲン酸類の質量比率、即ち、(A3)/[(A1)+(A2)+(A3)]が0.06〜0.13、より好ましくは0.08〜0.127、更に好ましくは0.1〜0.12であることが、保存安定性と風味バランスを制御し易い点から好ましい。
The packaged milk coffee beverage of the present invention contains chlorogenic acids in an amount of 0.14 to 0.5% by mass (hereinafter simply referred to as “%” unless otherwise specified) from the viewpoints of physiological effect, flavor, and stability. It contains 0.145 to 0.4%, more preferably 0.15 to 0.37%, still more preferably 0.155 to 0.36%, and particularly preferably 0.16 to 0.2%. The chlorogenic acids include (A 1 ) monocaffeoylquinic acid, (A 2 ) ferulaquinic acid, and (A 3 ) dicaffeoylquinic acid. Here, (A 1 ) monocaffeoylquinic acid includes at least one selected from 3-caffeoylquinic acid, 4-caffeoylquinic acid and 5-caffeoylquinic acid. Examples of (A 2 ) ferulquinic acid include one or more selected from 3-ferlaquinic acid, 4-ferlaquinic acid and 5-ferlaquinic acid. (A 3 ) Examples of dicaffeoylquinic acid include one or more selected from 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid, and 4,5-dicaffeoylquinic acid. The content of the chlorogenic acids can be measured by high performance liquid chromatography (HPLC). As a detection means in HPLC, it can be detected by UV detection. Furthermore, chlorogenic acids can be detected with high sensitivity by CL (chemiluminescence) detection, EC (electrochemistry) detection, LC-Mass detection, or the like.
In the present invention, the mass ratio of dichlorogenic acids / chlorogenic acids, that is, (A 3 ) / [(A 1 ) + (A 2 ) + (A 3 )] is 0.06 to 0.13, more preferably 0. It is preferably from 0.08 to 0.127, more preferably from 0.1 to 0.12, from the viewpoint of easy control of storage stability and flavor balance.

本発明の容器詰ミルクコーヒー飲料は、H22(過酸化水素)の含有量が1ppm以下、更に0.1ppm以下、特に0.01ppm以下であるのがコーヒー本来の風味の点で好ましい。過酸化水素の測定は通常用いられる過酸化水素計を用いて行うことができ、例えば、セントラル科学社製の高感度過酸化水素計スーパーオリテクターモデル5(SUPER ORITECTOR MODEL5)等を用いることができる。 The content of H 2 O 2 (hydrogen peroxide) in the container-packed milk coffee beverage of the present invention is preferably 1 ppm or less, more preferably 0.1 ppm or less, and particularly preferably 0.01 ppm or less from the viewpoint of the original flavor of coffee. The measurement of hydrogen peroxide can be performed using a commonly used hydrogen peroxide meter. For example, a high-sensitivity hydrogen peroxide meter Super Orientor Model 5 (SUPER ORITECTOR MODEL 5) manufactured by Central Science Co., Ltd. can be used. .

本発明で用いられる焙煎コーヒー豆から得られるコーヒー抽出物は、コーヒー豆からの抽出物、インスタントコーヒーの水溶液、液体コーヒーエキスなどから調製することができる。
本発明におけるコーヒー抽出物を得るのに用いるコーヒー豆の種類は、例えばブラジル、コロンビア、タンザニア、モカ、キリマンジェロ、マンデリン、ブルーマウンテン等が挙げられる。コーヒー豆種としては、アラビカ種、ロブスタ種などがある。コーヒー豆は1種でもよいし、複数種をブレンドして用いてもよい。コーヒー豆を焙煎により焙煎コーヒー豆とする方法については、好ましい焙煎方法としては直火式又は熱風式、半熱風式があり、回転ドラムを有している形式が更に好ましい。焙煎温度は通常100〜300℃、更に好ましくは150〜250℃である。風味の観点より焙煎後1時間以内に0〜100℃まで冷却することが好ましく、更に好ましくは10〜60℃である。焙煎コーヒー豆の焙煎度としては、ライト、シナモン、ミディアム、ハイ、シティ、フルシティ、フレンチ、イタリアンがあり、ライト、シナモン、ミディアム、ハイ、シティが好ましい。
焙煎度を色差計で測定したL値としては、60以下、好ましくは10〜50、更に好ましくは15〜25である。また、焙煎度の違うコーヒー豆由来の抽出物を混合して使用するのが好ましい。その場合にはL値40〜60の焙煎度を持つコーヒー豆由来の抽出物とL10〜39の焙煎度を持つコーヒー豆由来の抽出物を併用することができる。併用する場合には好ましくはL値35〜55の焙煎度を持つコーヒー豆由来の抽出物とL値15〜25の焙煎度を持つコーヒー豆由来の抽出物の併用、より好ましくはL値35〜53の焙煎度を持つコーヒー豆由来の抽出物とL値16〜24の焙煎度を持つコーヒー豆由来の抽出物の併用、もっとも好ましくはL値36〜51の焙煎度を持つコーヒー豆由来の抽出物とL値16.5〜22の焙煎度を持つコーヒー豆由来の抽出物の併用が良い。また、焙煎度の異なるコーヒー豆由来の抽出物を併用する場合や単独で使用する場合に、生コーヒー豆からの抽出物を焙煎コーヒー豆と併せて使用してもよい。
The coffee extract obtained from roasted coffee beans used in the present invention can be prepared from an extract from coffee beans, an aqueous solution of instant coffee, a liquid coffee extract and the like.
Examples of the type of coffee beans used to obtain the coffee extract in the present invention include Brazil, Colombia, Tanzania, mocha, kilimangelo, mandelin, blue mountain and the like. Coffee beans include Arabica and Robusta. One kind of coffee beans may be used, or a plurality of kinds may be blended. About the method of making coffee beans into roasted coffee beans by roasting, preferred roasting methods include direct fire type, hot air type, and semi-hot air type, and a type having a rotating drum is more preferred. The roasting temperature is usually 100 to 300 ° C, more preferably 150 to 250 ° C. From the viewpoint of flavor, it is preferable to cool to 0 to 100 ° C. within 1 hour after roasting, more preferably 10 to 60 ° C. As roasting degree of roasted coffee beans, there are light, cinnamon, medium, high, city, full city, french and italian, and light, cinnamon, medium, high and city are preferred.
As L value which measured the roasting degree with the color difference meter, it is 60 or less, Preferably it is 10-50, More preferably, it is 15-25. In addition, it is preferable to mix and use extracts derived from coffee beans having different roasting degrees. In that case, an extract derived from coffee beans having a roasting degree of L value 40 to 60 and an extract derived from coffee beans having a roasting degree L10 to 39 can be used in combination. When used in combination, preferably an extract derived from coffee beans having a roasting degree of L value 35 to 55 and an extract derived from coffee beans having a roasting degree L value of 15 to 25, more preferably L value Combined use of an extract derived from coffee beans having a roasting degree of 35-53 and an extract derived from coffee beans having an roasting degree of 16-24, most preferably having a roasting degree of 36-51 L A combination of an extract derived from coffee beans and an extract derived from coffee beans having an L value of 16.5 to 22 is preferable. Moreover, when using together the extract derived from the coffee beans from which a roasting degree differs, or using it independently, you may use the extract from a green coffee bean together with roasted coffee beans.

焙煎コーヒー豆からの抽出方法については、、例えば焙煎コーヒー豆又はその粉砕物から水〜熱水(0〜100℃)などの抽出溶媒を用いて抽出する方法等が挙げられる。粉砕度合いは、極細挽き(0.250-0.500μm)、細挽き(0.300-0.650μm)、中細挽き(0.530-1.000μm)、中挽き(0.650-1.500μm)、粗挽き(0.850-2.100μm)、極粗挽き(1.000-2.500μm)や平均粒径3〜10mm程度の粉砕物をカットしたものが挙げられる。コーヒーの抽出方法は、ボイリング式、エスプレッソ式、サイホン式、ドリップ式(ペーパー、ネル等)等が挙げられる。また生コーヒー豆から抽出物を得る場合も上記方法から選択しても良い。   About the extraction method from roasted coffee beans, the method of extracting from roasted coffee beans or its ground material using extraction solvents, such as water-hot water (0-100 degreeC), etc. are mentioned, for example. The degree of grinding is as follows: extra fine grinding (0.250-0.500μm), fine grinding (0.300-0.650μm), medium fine grinding (0.530-1.000μm), medium grinding (0.650-1.500μm), coarse grinding (0.850-2.100μm), Examples include extremely coarse grinding (1.000-2.500 μm) and pulverized products having an average particle diameter of about 3 to 10 mm. Examples of the coffee extraction method include a boiling type, an espresso type, a siphon type, and a drip type (paper, flannel, etc.). Moreover, when obtaining an extract from green coffee beans, the above method may be selected.

抽出溶媒としては、水、アルコール含有水、ミルク、炭酸水などが挙げられる。抽出溶媒のpHは通常4〜10であり、風味の観点からは5〜7が好ましい。尚、抽出溶媒の中にpH調整剤、例えば重炭酸水素ナトリウム、炭酸水素ナトリウム、L−アスコルビン酸、L−アルコルビン酸Naを含有させ、pHを適宜調整しても良い。   Examples of the extraction solvent include water, alcohol-containing water, milk, carbonated water, and the like. The pH of the extraction solvent is usually 4 to 10, and 5 to 7 is preferable from the viewpoint of flavor. In addition, a pH adjusting agent such as sodium bicarbonate, sodium bicarbonate, L-ascorbic acid, or L-alcorbic acid Na may be contained in the extraction solvent, and the pH may be adjusted appropriately.

コーヒー抽出器としては、ペーパードリップ、不織布ドリップ、サイフォン、ネルドリップ、エスプレッソマシン、パーコレーター、コーヒープレス、イブリック、ウォータードリップ、ボイリング、加熱可能な釜、攪拌及び攪拌可能な釜、コーヒーカップへ実質的に懸架可能なペーパー又は不織布の袋状構造体、上部にスプレーノズル下部に実質的にコーヒー豆の固液分離可能な構造体(メッシュやパンチングメタルなど)を有するドリップ抽出器、上部及び下部に実質的にコーヒー豆の固液分離可能な構造体(メッシュやパンチングメタルなど)を有するカラム抽出器等が挙げられる。抽出器に加熱又は冷却可能な構造(例えば、電気ヒーター、温水や蒸気、冷水が通液可能なジャケット)を有していても良い。   As a coffee extractor, paper drip, non-woven drip, siphon, nel drip, espresso machine, percolator, coffee press, ibrick, water drip, boiling, heatable kettle, stirring and stirrable kettle, coffee cup substantially Suspendable paper or non-woven bag-like structure, drip extractor having a structure capable of solid-liquid separation of coffee beans (mesh, punching metal, etc.) substantially above the spray nozzle at the top, substantially above and below Column extractor having a structure (mesh, punching metal, etc.) capable of solid-liquid separation of coffee beans. The extractor may have a structure that can be heated or cooled (for example, an electric heater, a jacket through which hot water, steam, or cold water can flow).

抽出方法としてはバッチ式抽出法、半バッチ式抽出法、連続式抽出法が挙げられる。バッチ式抽出法又は半バッチ式抽出法の抽出時間は10秒〜120分である。風味の観点より、30秒から30分が好ましい。   Examples of the extraction method include a batch extraction method, a semi-batch extraction method, and a continuous extraction method. The extraction time of the batch type extraction method or the semi-batch type extraction method is 10 seconds to 120 minutes. From the viewpoint of flavor, 30 seconds to 30 minutes is preferable.

コーヒー抽出液を活性炭処理することが好ましい。例えば、バッチ法としては、例えばコーヒー抽出液を含む液に活性炭を加え−10〜100℃で0.5分〜5時間撹拌した後、活性炭を除去すればよい。処理時の雰囲気としては、空気下、不活性ガス下(窒素ガス、アルゴンガス、ヘリウムガス、炭酸ガス)が挙げられるが、風味の観点より不活性ガス下が好ましい。
カラム通液法としては、例えば活性炭カラム内に活性炭を充填し、コーヒー抽出液を含む液をカラム下部又は上部から通液させ、他方から排出させる。活性炭のカラム内への充填量は、通液前に活性炭カラムに充填できる量であれば良い。活性炭カラムの上段又は下段の少なくとも1つにメッシュ(網)又はパンチングメタルなど有し実質的に活性炭が漏れ出さない分離構造体を有していれば良い。
The coffee extract is preferably treated with activated carbon. For example, as a batch method, for example, activated carbon may be added to a liquid containing a coffee extract and stirred at −10 to 100 ° C. for 0.5 minutes to 5 hours, and then the activated carbon may be removed. Examples of the atmosphere during the treatment include air and inert gas (nitrogen gas, argon gas, helium gas, carbon dioxide gas), but inert gas is preferred from the viewpoint of flavor.
As the column flow method, for example, activated carbon is filled in an activated carbon column, and a liquid containing a coffee extract is passed from the bottom or top of the column and discharged from the other. The amount of the activated carbon packed in the column may be an amount that can be packed in the activated carbon column before passing. It is sufficient that at least one of the upper and lower stages of the activated carbon column has a separation structure that has a mesh or a punching metal and does not substantially leak the activated carbon.

活性炭量は、コーヒー抽出液中のコーヒー豆由来可溶性固形分(Brix)に対して、0.01〜100倍である。風味の観点より、活性炭の場合は、0.02〜1.0倍用いるのが好ましい。   The amount of activated carbon is 0.01 to 100 times the coffee bean-derived soluble solid content (Brix) in the coffee extract. From the viewpoint of flavor, in the case of activated carbon, it is preferable to use 0.02 to 1.0 times.

活性炭としては、ミクロ孔領域における平均細孔半径が5オングストローム(Å)以下、更には、2〜5オングストロームの範囲であることが好ましく、特に3〜5オングストロームの範囲であることが好ましい。本発明におけるミクロ孔領域とは、10オングストローム以下を示し、平均細孔半径は、MP法により測定して得た細孔分布曲線のピークトップを示す細孔半径の値とした。MP法とは、文献(Colloid and Interface Science, 26, 46(1968))に記載の細孔測定法であり、株式会社住化分析センター、株式会社東レリサーチセンターにて採用されている方法である。
また、活性炭の種類としては、ヤシ殻活性炭が好ましく、更に水蒸気賦活化ヤシ殻活性炭が好ましい。活性炭の市販品としては、白鷺WH2C、WH2CL、W2CL、W2C、EH(日本エンバイロケミカルズ)、太閣CW(二村化学)、クラレコールGW(クラレケミカル)等を用いることができる。
活性炭を用いた吸着剤処理法はクロロゲン酸類量を低下させることなく選択的にヒドロキシヒドロキノン含量を低減させることができるだけでなく、風味も良く、更に、カリウム含量を低下させない点からも好ましい。
尚、吸着剤処理工程は、コーヒー抽出液のみで処理をおこなうのが好適であるが、原料、例えば炭酸水素ナトリウムなどを混合し処理をおこなっても良い。
As the activated carbon, the average pore radius in the micropore region is preferably 5 angstroms (Å) or less, more preferably in the range of 2 to 5 angstroms, and particularly preferably in the range of 3 to 5 angstroms. In the present invention, the micropore region indicates 10 angstroms or less, and the average pore radius is a value of the pore radius indicating the peak top of the pore distribution curve obtained by measurement by the MP method. The MP method is a pore measurement method described in the literature (Colloid and Interface Science, 26, 46 (1968)), and is a method adopted by Sumika Chemical Analysis Center, Inc. and Toray Research Center, Inc. .
Moreover, as a kind of activated carbon, coconut shell activated carbon is preferable, and also water vapor activated coconut shell activated carbon is preferable. As a commercially available product of activated carbon, Shirakaba WH2C, WH2CL, W2CL, W2C, EH (Nippon Envirochemicals), Taiko CW (Nikamura Chemical), Kuraray Coal GW (Kuraray Chemical), etc. can be used.
The adsorbent treatment method using activated carbon is preferable not only because it can selectively reduce the hydroxyhydroquinone content without reducing the amount of chlorogenic acids, but also because it has a good flavor and does not reduce the potassium content.
The adsorbent treatment step is preferably performed only with the coffee extract, but may be performed by mixing raw materials such as sodium hydrogen carbonate.

本発明の容器詰ミルクコーヒー飲料のクロロゲン酸類/タンニン(FOLIN−DENIS法)質量比率は0.6〜0.97、好ましくは0.62〜0.9、更に好ましくは0.65〜0.78が好適である。この範囲にあると焙煎豆由来の風味が温存されると共にクロロゲン酸類濃度が高いながらも保存安定性が向上し良い。
本発明の容器詰ミルクコーヒー飲料のキナ酸の含有量は0.021〜0.2g/100g、好ましくは0.05〜0.15g/100g、より好ましくは0.08〜0.14g/100gが風味と安定性のバランスより好ましい。キナ酸はコーヒー豆の焙煎温度や時間により、コーヒー豆中での含有量が複雑に変わる。また、コーヒー抽出液中においても、抽出条件によっても変化する(コーヒー焙煎の化学と技術 1995年2月28日初版発行、弘学出版株式会社発行)。また、コーヒー飲料中のキナ酸量は、コーヒー飲料の保存時のpHや酸味に影響を及ぼす。本発明においては、0.021g/100g未満であれば、ミルクコーヒー飲料の酸味に欠ける。また、0.2g/100gを超えると、ミルクコーヒー飲料の安定性が悪くなる。
The chlorogenic acids / tannin (FOLIN-DENIS method) mass ratio of the packaged milk coffee beverage of the present invention is 0.6 to 0.97, preferably 0.62 to 0.9, more preferably 0.65 to 0.78. Is preferred. Within this range, the flavor derived from roasted beans can be preserved and the storage stability can be improved while the concentration of chlorogenic acids is high.
The content of quinic acid in the containered milk coffee beverage of the present invention is 0.021 to 0.2 g / 100 g, preferably 0.05 to 0.15 g / 100 g, more preferably 0.08 to 0.14 g / 100 g. More preferable than the balance between flavor and stability. The content of quinic acid in the coffee beans varies depending on the roasting temperature and time of the coffee beans. Also in the coffee extract, it varies depending on the extraction conditions (chemistry and technology of roasted coffee published on February 28, 1995, published by Kogaku Publishing Co., Ltd.). Further, the amount of quinic acid in the coffee beverage affects the pH and sourness of the coffee beverage during storage. In this invention, if it is less than 0.021 g / 100g, the acidity of a milk coffee drink will be lacking. Moreover, when it exceeds 0.2g / 100g, stability of a milk coffee drink will worsen.

本発明の容器詰ミルクコーヒー飲料は、高速液体クロマトグラフィーによる分析における、ガリックアシッドを標準物質とした場合のガリックアシッドに対する相対保持時間が0.54〜0.61の時間領域に実質的にピークを有しないことが好ましい。当該時間領域に実質的にピークを有しないことを確認するには、一般的なHPLCを使用することができ、例えば溶離液として0.05M酢酸水溶液と0.05M酢酸100%アセトニトリル溶液のグラジエントを用い、ODSカラムを用いて、紫外線吸光光度計等により検出することで確認することができる。   The packaged milk coffee beverage of the present invention has a peak substantially in the time range of 0.54 to 0.61 relative retention time with respect to gallic acid when gallic acid is used as a standard substance in analysis by high performance liquid chromatography. It is preferable not to have. In order to confirm that there is substantially no peak in the time domain, general HPLC can be used. For example, a gradient of 0.05 M acetic acid aqueous solution and 0.05 M acetic acid 100% acetonitrile solution is used as an eluent. It can be confirmed by using an ODS column and detecting with an ultraviolet absorptiometer or the like.

本発明においてガリックアシッドに対する相対保持時間が0.54〜0.61の時間領域に実質的にピークを有しないとは、ガリックアシッドの1ppm溶液を分析時の面積値をS1とし、同条件でコーヒー飲料組成物を分析した時の前記特定の領域に溶出する成分に由来するピーク面積の総和をS2としたとき、S2/S1<0.01であることを意味する。   In the present invention, the fact that the relative retention time with respect to gallic acid does not substantially have a peak in the time range of 0.54 to 0.61 means that the area value at the time of analysis of a 1 ppm solution of gallic acid is S1, When the sum of the peak areas derived from the components eluted in the specific region when the beverage composition is analyzed is S2, it means that S2 / S1 <0.01.

本発明の容器詰ミルクコーヒー飲料は、F0値(致死値)を一定値以上に設定して加熱殺菌処理を行うことにより製造される。F0値は、微生物学的安定性の点で、5〜60、好ましくは10〜50、より好ましくは15〜40、更に好ましくは17〜35である。ここで、F0値とは、缶詰コーヒー飲料を加熱殺菌した場合の加熱殺菌効果を評価する値で、基準温度(121.1℃)における加熱時間(分)を示す。F0値は、容器内温度に対する致死率(121.1℃で1)に、加熱時間(分)を乗じて算出される。致死率は致死率表(藤巻正生ら、「食品工業」、恒星社厚生閣、1985年、1049頁)から求めることができる。F0値を算出するには、一般的に用いられる面積計算法、公式法等を採用することができる(例えば谷川ら《缶詰製造学》頁220、厚生閣 参照)。
本発明において、F0値を所定の値になるよう設定するには、例えば、予め得た致死率
曲線から、適当な加熱温度・加熱時間を決定すればよい。
The packaged milk coffee beverage of the present invention is produced by performing a heat sterilization treatment with the F0 value (lethal value) set to a certain value or more. The F0 value is 5 to 60, preferably 10 to 50, more preferably 15 to 40, and still more preferably 17 to 35 in terms of microbiological stability. Here, the F0 value is a value for evaluating the heat sterilization effect when the canned coffee beverage is heat sterilized, and indicates the heating time (minutes) at the reference temperature (121.1 ° C.). The F0 value is calculated by multiplying the lethality rate (1 at 121.1 ° C.) with respect to the temperature in the container by the heating time (minutes). The fatality rate can be obtained from the fatality rate table (Masao Fujimaki et al., “Food Industry”, Hoshiseisha Koseikaku, 1985, page 1049). In order to calculate the F0 value, a commonly used area calculation method, formula method, or the like can be employed (see, for example, Tanikawa et al. << Canned Manufacturing Science >> page 220, Koseikaku).
In the present invention, in order to set the F0 value to be a predetermined value, for example, an appropriate heating temperature and heating time may be determined from a preliminarily obtained lethality curve.

殺菌機はバッチ式殺菌機又は連続式殺菌機が使用可能である。バッチ式殺菌機としては、レトルト釜がある。連続式殺菌機としては、チューブ式殺菌機、プレート式殺菌機、HTSTプレート式殺菌装置、UHT殺菌機などがある(改訂版ソフトドリンクス、頁546−558、頁633−638、監修:全国清涼飲料工業会、発行:光琳)。風味の観点より、連続殺菌機が好ましく。特に、連続加熱殺菌後無菌下で充填することが好ましい。   As the sterilizer, a batch sterilizer or a continuous sterilizer can be used. There is a retort pot as a batch type sterilizer. Continuous sterilizers include tube-type sterilizers, plate-type sterilizers, HTST plate-type sterilizers, UHT sterilizers, etc. (revised soft drinks, pages 546-558, pages 633-638, supervised by Seiyo Nationwide) Beverage Manufacturers Association, published by Korin). From the viewpoint of flavor, a continuous sterilizer is preferred. In particular, it is preferable to fill under aseptic conditions after continuous heat sterilization.

また本発明において、殺菌時間は、ヒドロキシヒドロキノンの増加を効果的に抑制する点で、10分以内であり、好ましくは100秒〜9分、より好ましくは110秒〜8分である。   In the present invention, the sterilization time is within 10 minutes, preferably from 100 seconds to 9 minutes, more preferably from 110 seconds to 8 minutes, from the viewpoint of effectively suppressing an increase in hydroxyhydroquinone.

また、殺菌温度は、微生物学的安定性の点で123℃以上が好ましく、更に123〜150℃、より好ましくは126〜141℃、更に好ましくは129〜140℃が好適である。またF0は少なくとも5以上にする必要がある。   The sterilization temperature is preferably 123 ° C. or higher in view of microbiological stability, more preferably 123 to 150 ° C., more preferably 126 to 141 ° C., and still more preferably 129 to 140 ° C. Further, F0 needs to be at least 5 or more.

当該加熱殺菌処理は、上記条件の他、金属缶のように容器に充填後、加熱殺菌できる場合にあっては食品衛生法に定められた殺菌条件で行われる。また加熱殺菌設定条件までの昇温及び冷却は速やかに行ない、過剰な熱履歴を伴わないように留意すべきである。尚、金属缶においても加熱殺菌後の充填でもよい。また、紙、瓶等においても同様であり、容器の耐熱性を勘案し、充填後加熱殺菌でも加熱殺菌後充填でも可能である。   In addition to the above conditions, the heat sterilization treatment is performed under the sterilization conditions stipulated in the Food Sanitation Law if the container can be heat sterilized after being filled into a container like a metal can. Also, it should be noted that the temperature rise and cooling to the heat sterilization setting conditions should be performed promptly and not accompanied by excessive heat history. In addition, the metal can may be filled after heat sterilization. The same applies to paper, bottles, and the like, and heat sterilization after filling or filling after heat sterilization is possible considering the heat resistance of the container.

本発明の容器詰ミルクコーヒー飲料には、ショ糖、グルコース、フルクトース、キシロース、果糖ブドウ糖液、糖アルコール等の糖分、抗酸化剤、pH調整剤、乳化剤、香料等を添加することができる。コーヒー組成物のpHとしては、飲料の風味及び安定性の面から5〜7、更に5.5〜6.9、特に6.0〜6.7が好ましい。本発明の容器詰ミルクコーヒー飲料には、乳成分としては、生乳、牛乳、全粉乳、脱脂粉乳、生クリーム、濃縮乳、脱脂乳、部分脱脂乳、練乳等を配合できる。これらの乳成分は、合計で容器詰ミルクコーヒー飲料中に乳固形分換算で0.1〜10%、さらに0.5〜6%、特に1〜4%含有するのが好ましい。   Sugars such as sucrose, glucose, fructose, xylose, fructose glucose solution, sugar alcohol, antioxidants, pH adjusters, emulsifiers, fragrances, and the like can be added to the packaged milk coffee beverage of the present invention. The pH of the coffee composition is preferably 5 to 7, more preferably 5.5 to 6.9, and particularly preferably 6.0 to 6.7 from the viewpoint of beverage flavor and stability. In the container-packed milk coffee beverage of the present invention, raw milk, cow milk, whole milk powder, skim milk powder, fresh cream, concentrated milk, skimmed milk, partially skimmed milk, condensed milk, and the like can be blended as milk components. These milk components are preferably contained in a total amount of 0.1 to 10%, further 0.5 to 6%, particularly 1 to 4% in terms of milk solid content in the containered milk coffee beverage.

本発明の容器詰ミルクコーヒー飲料は、缶(アルミニウム、スチール)、紙、レトルトパウチ、瓶(ガラス)等の容器に詰めて製造することができる。この場合、容器に詰めて50〜500mLの缶詰ミルクコーヒー飲料とすることができる。缶詰ミルクコーヒー飲料は、シングルストレングスであることが好ましい。ここでシングルストレングスとは、容器詰飲料を開封した後、そのまま飲めるものをいう。また、本発明により得られる缶詰ミルクコーヒー飲料中のモノカフェオイルキナ酸の構成比としては、4−カフェオイルキナ酸/3−カフェオイルキナ酸質量比率が0.6〜1.2であり、5−カフェオイルキナ酸/3−カフェオイルキナ酸質量比率が0.01〜3であることが好ましい。   The packaged milk coffee beverage of the present invention can be produced by filling a container such as a can (aluminum, steel), paper, a retort pouch, a bottle (glass) or the like. In this case, the container can be packed into a 50 to 500 mL canned milk coffee drink. The canned milk coffee beverage is preferably single-strength. Here, “single strength” refers to what can be drunk as it is after opening the packaged beverage. Moreover, as a constituent ratio of monocaffeoylquinic acid in the canned milk coffee beverage obtained by the present invention, the 4-caffeoylquinic acid / 3-caffeoylquinic acid mass ratio is 0.6 to 1.2, The mass ratio of 5-caffeoylquinic acid / 3-caffeoylquinic acid is preferably 0.01 to 3.

容器としては、コーヒー中の成分の変化を防止する観点から、酸素透過度の低い容器が好ましく、例えば、アルミニウムや、スチールなどの缶、ガラス製の瓶等を用いるのが良い。缶やビンの場合、リキャップ可能な、リシール型のものも含まれる。ここで酸素透過性とは、20℃、相対湿度50%の環境下で測定した酸素透過度(cc・mm/m2・day・atm)であり、酸素透過度が5以下が好ましく、更に3以下、特に1以下が好ましい。 As the container, a container having a low oxygen permeability is preferable from the viewpoint of preventing changes in the ingredients in the coffee. For example, a can made of aluminum or steel, a glass bottle, or the like may be used. In the case of cans and bottles, resealable ones that can be recapped are also included. Here, the oxygen permeability is an oxygen permeability (cc · mm / m 2 · day · atm) measured in an environment of 20 ° C. and a relative humidity of 50%, and the oxygen permeability is preferably 5 or less. Hereinafter, 1 or less is particularly preferable.

クロロゲン酸類の分析法:
容器詰ミルクコーヒー飲料のクロロゲン酸類の分析法は次の通りである。分析機器はHPLCを使用した。装置の構成ユニットの型番は次の通り。UV−VIS検出器:L−2420((株)日立ハイテクノロジーズ)、カラムオーブン:L−2300((株)日立ハイテクノロジーズ)、ポンプ:L−2130((株)日立ハイテクノロジーズ)、オートサンプラー:L−2200((株)日立ハイテクノロジーズ)、カラム:Cadenza CD−C18 内径4.6mm×長さ150mm、粒子径3μm(インタクト(株))。
分析条件は次の通りである。サンプル注入量:10μL、流量:1.0mL/min、UV−VIS検出器設定波長:325nm、カラムオーブン設定温度:35℃、溶離液A:0.05M 酢酸、0.1mM 1−ヒドロキシエタン−1,1−ジホスホン酸、10mM 酢酸ナトリウム、5(V/V)%アセトニトリル溶液、溶離液B:アセトニトリル。
Analysis of chlorogenic acids:
A method for analyzing chlorogenic acids in a packaged milk coffee beverage is as follows. The analytical instrument used was HPLC. The model numbers of the unit units are as follows. UV-VIS detector: L-2420 (Hitachi High-Technologies Corporation), column oven: L-2300 (Hitachi High-Technologies Corporation), pump: L-2130 (Hitachi High-Technologies Corporation), autosampler: L-2200 (Hitachi High-Technologies Corporation), column: Cadenza CD-C18 inner diameter 4.6 mm × length 150 mm, particle diameter 3 μm (intact Inc.).
The analysis conditions are as follows. Sample injection volume: 10 μL, flow rate: 1.0 mL / min, UV-VIS detector set wavelength: 325 nm, column oven set temperature: 35 ° C., eluent A: 0.05 M acetic acid, 0.1 mM 1-hydroxyethane-1 , 1-diphosphonic acid, 10 mM sodium acetate, 5 (V / V)% acetonitrile solution, eluent B: acetonitrile.

濃度勾配条件
時間 溶離液A 溶離液B
0.0分 100% 0%
10.0分 100% 0%
15.0分 95% 5%
20.0分 95% 5%
22.0分 92% 8%
50.0分 92% 8%
52.0分 10% 90%
60.0分 10% 90%
60.1分 100% 0%
70.0分 100% 0%
Concentration gradient condition Time Eluent A Eluent B
0.0 minutes 100% 0%
10.0 minutes 100% 0%
15.0 minutes 95% 5%
20.0 minutes 95% 5%
22.0 minutes 92% 8%
50.0 minutes 92% 8%
52.0 minutes 10% 90%
60.0 minutes 10% 90%
60.1 minutes 100% 0%
70.0 minutes 100% 0%

HPLCでは、試料1gを精秤後、溶離液Aにて10mLにメスアップし、メンブレンフィルター(GLクロマトディスク25A,孔径0.45μm,ジーエルサイエンス(株))にて濾過後、分析に供した。
クロロゲン酸類の保持時間(単位:分)
(A1)モノカフェオイルキナ酸:5.3、8.8、11.6の計3点(A2)フェルラキナ酸:13.0、19.9、21.0の計3点(A3)ジカフェオイルキナ酸:36.6、37.4、44.2の計3点。ここで求めた9種のクロロゲン酸類の面積値から5−カフェオイルキナ酸を標準物質とし、質量%を求めた。
In HPLC, 1 g of a sample was precisely weighed, made up to 10 mL with eluent A, filtered through a membrane filter (GL chromatodisc 25A, pore size 0.45 μm, GL Sciences Inc.), and subjected to analysis.
Retention time of chlorogenic acids (unit: minutes)
(A 1 ) Monocafe oil quinic acid: 5.3, 8.8, 11.6, total 3 points (A 2 ) Ferlaquinic acid: 13.0, 19.9, 21.0, total 3 points (A 3 ) Dicaffeoylquinic acid: 36.6, 37.4, 44.2 in total. From the area values of the nine types of chlorogenic acids determined here, 5-caffeoylquinic acid was used as a standard substance, and the mass% was determined.

タンニン(FOLIN−DENIS法)の分析方法:
ミルクコーヒー飲料の測定法
サンプルとなるコーヒー液をS(g)採取し、イオン交換水でV(ml)に定容する。定容した液を検液として、これを5ml分取する。次に、Folin試薬:5mlと、10%炭酸ナトリウム溶液:5mlを検液と混和し、反応を開始する。この反応液を室温で1時間放置する。
反応後、反応液中の濁り成分を除くため、シリンジ(テルモ社製、5ml用)に、フィルター(GLサイエンス社製、水系/25A/孔径0.45μm)を取り付け、反応後の検液を押し出してろ過する。ろ液の吸光値を波長:700nmで測定する。以下の計算式でタンニン(タンニン酸として)濃度を計算する。
タンニン(g/100g)=A×V/5×B×10-6×100/S
(A:タンニン酸濃度(μg/発色液)、B:希釈倍率)
参考文献:五訂 日本食品標準成分表 分析マニュアルの解説
財団法人 日本食品分析センター編集/ 中央法規
Analytical method of tannin (FOLIN-DENIS method):
Measuring method of milk coffee beverage Take S (g) of sample coffee liquid and make up to V (ml) with ion-exchanged water. Using a fixed volume as a test solution, take 5 ml of this solution. Next, 5 ml of Folin reagent and 5 ml of 10% sodium carbonate solution are mixed with the test solution to start the reaction. The reaction is left at room temperature for 1 hour.
To remove turbid components in the reaction solution after the reaction, attach a filter (GL Science, water / 25A / pore size 0.45μm) to a syringe (manufactured by Terumo, 5ml), and push the test solution after reaction. Filter. The absorbance value of the filtrate is measured at a wavelength of 700 nm. Calculate the tannin (as tannic acid) concentration with the following formula.
Tannin (g / 100g) = A x V / 5 x B x 10 -6 x 100 / S
(A: Tannic acid concentration (μg / color developing solution), B: Dilution factor)
References: Five revisions Japanese food standard ingredient table Explanation of analysis manual
Edited by Japan Food Analysis Center / Central Law

キナ酸の分析方法
検体2gを超音波処理後濾過し、高速液体クロマトグラフで測定した。
機種:LC−10AD(島津製作所(株))
検出器:紫外可視分光光度計 SPD−10AVvp(島津製作所(株))
カラム:Shodex RSpak C−811,φ8mm×500mm(昭和電工(株))
カラム温度:60℃
移動相:3mmol/L過塩素酸
反応液:0.2mmol/Lブロムチモールブルー含有
15mmol/Lリン酸水素ニナトリウム溶液
流量:移動相1.0mL/min、反応液1.4mL/min
測定波長:445nm
(出典:食品衛生検査指針 食品添加物編 2003年度版)
Analytical method of quinic acid 2 g of a specimen was filtered after sonication and measured with a high performance liquid chromatograph.
Model: LC-10AD (Shimadzu Corporation)
Detector: UV-visible spectrophotometer SPD-10AVvp (Shimadzu Corporation)
Column: Shodex RSpak C-811, φ8 mm × 500 mm (Showa Denko KK)
Column temperature: 60 ° C
Mobile phase: 3 mmol / L perchloric acid reaction solution: 0.2 mmol / L containing bromothymol blue
15 mmol / L disodium hydrogen phosphate solution flow rate: mobile phase 1.0 mL / min, reaction solution 1.4 mL / min
Measurement wavelength: 445 nm
(Source: Food Sanitation Inspection Guidelines, Food Additives Edition 2003)

実施例1
高焙煎度(L値 16.5)のコーヒー豆より得た抽出液のBrixに対して、重量比で50%の活性炭を充填したカラムに室温、SV20[1/容量[m]/流量[m/hr]]の条件下で、前記コーヒー抽出液を処理した。同様に、低焙煎度のコーヒー豆(L値 35)より得た抽出液を活性炭処理カラムに通液処理した。得られた活性炭処理液を表1に示す配合割合で混合し、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、129℃で7分間の殺菌を行った。
実施例2
牛乳の配合量を表1に示すように変えた以外は実施例1と同様にして容器詰ミルクコーヒー飲料を得た。
実施例3
活性炭処理液の配合量を表1に示すように変えた以外は実施例1と同様にして容器詰ミルクコーヒー飲料を得た。
実施例4
缶容器に充填、密封後の殺菌条件を135℃で1分40秒間とした以外は実施例1と同様にして容器詰ミルクコーヒー飲料を得た。
実施例5
缶容器に充填、密封後の殺菌条件を135℃で1分40秒間とした以外は実施例2と同様にして容器詰ミルクコーヒー飲料を得た。
実施例6
缶容器に充填、密封後の殺菌条件を135℃で1分40秒間とした以外は実施例3と同様にして容器詰ミルクコーヒー飲料を得た。
Example 1
SV20 [1 / volume [m 3 ] / flow rate at room temperature in a column packed with 50% activated carbon by weight with respect to Brix of the extract obtained from coffee beans with high roasting degree (L value 16.5) The coffee extract was treated under the conditions of [m 3 / hr]. Similarly, the extract obtained from coffee beans with low roasting degree (L value 35) was passed through an activated carbon treatment column. The obtained activated carbon treatment liquid is mixed at a blending ratio shown in Table 1, and after adding auxiliary materials such as sugar and milk, pH is adjusted with an aqueous solution in which sodium hydrogen carbonate is dissolved. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and sterilized at 129 ° C. for 7 minutes.
Example 2
A packaged milk coffee beverage was obtained in the same manner as in Example 1 except that the blending amount of milk was changed as shown in Table 1.
Example 3
A packaged milk coffee beverage was obtained in the same manner as in Example 1 except that the amount of the activated carbon treatment liquid was changed as shown in Table 1.
Example 4
A canned milk coffee beverage was obtained in the same manner as in Example 1 except that the sterilization conditions after filling and sealing the can container were set at 135 ° C. for 1 minute and 40 seconds.
Example 5
A canned milk coffee beverage was obtained in the same manner as in Example 2 except that the sterilization conditions after filling and sealing the can container were set at 135 ° C. for 1 minute and 40 seconds.
Example 6
A canned milk coffee beverage was obtained in the same manner as in Example 3 except that the sterilization conditions after filling and sealing the can container were set at 135 ° C. for 1 minute and 40 seconds.

比較例1
中深焙煎度(L値 22)のコーヒー豆より得た抽出液について、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、118℃で10分間の殺菌を行った。
比較例2
中深焙煎度(L値 22)のコーヒー豆より得た抽出液のBrixに対して、重量比で50%の活性炭を充填したカラムに室温、SV20[1/容量[m]/流量[m/hr]]の条件下で、前記コーヒー抽出液を処理した。得られた活性炭処理液について、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、118℃で10分間の殺菌を行った。
比較例3
高焙煎度(L値 16.5)のコーヒー豆より得た抽出液のBrixに対して、重量比で50%の活性炭を充填したカラムに室温、SV20[1/容量[m]/流量[m/hr]]の条件下で、前記コーヒー抽出液を処理した。同様に、低焙煎度のコーヒー豆(L値 38)より得た抽出液を活性炭処理カラムに通液処理した。得られた活性炭処理液を表1に示す配合割合で混合し、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、129℃で7分間の殺菌を行った。
比較例4
比較例3と同様にして得られた活性炭処理液を表1に示す配合割合で混合し、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、129℃で7分間の殺菌を行った。
比較例5
極低焙煎度(L値 50)のコーヒー豆より得た抽出液のBrixに対して、重量比で50%の活性炭を充填したカラムに室温、SV20[1/容量[m]/流量[m/hr]]の条件下で、前記コーヒー抽出液を処理した。得られた活性炭処理液について、砂糖、牛乳などの副原料を配合後、炭酸水素ナトリウムを溶解した水溶液でpH調整する。そしてイオン交換水で希釈した。その後、本液を65℃まで加温しホモゲナイザーを通した。次に75℃まで加温し、190g入り缶容器に充填、密封後、129℃で7分間の殺菌を行った。
Comparative Example 1
About the extract obtained from the coffee beans of medium deep roasting degree (L value 22), pH is adjusted with the aqueous solution which melt | dissolved sodium hydrogencarbonate after mix | blending auxiliary materials, such as sugar and milk. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and then sterilized at 118 ° C. for 10 minutes.
Comparative Example 2
A column filled with 50% activated carbon by weight with respect to Brix of the extract obtained from coffee beans with a medium deep roasting degree (L value 22) at room temperature, SV20 [1 / volume [m 3 ] / flow rate [ m 3 / hr]]. The coffee extract was treated. About the obtained activated carbon processing liquid, after mix | blending auxiliary materials, such as sugar and milk, pH adjustment is carried out with the aqueous solution which melt | dissolved sodium hydrogencarbonate. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and then sterilized at 118 ° C. for 10 minutes.
Comparative Example 3
SV20 [1 / volume [m 3 ] / flow rate at room temperature in a column packed with 50% activated carbon by weight with respect to Brix of the extract obtained from coffee beans with high roasting degree (L value 16.5) The coffee extract was treated under the conditions of [m 3 / hr]. Similarly, the extract obtained from coffee beans with a low roasting degree (L value 38) was passed through an activated carbon treatment column. The obtained activated carbon treatment liquid is mixed at a blending ratio shown in Table 1, and after adding auxiliary materials such as sugar and milk, pH is adjusted with an aqueous solution in which sodium hydrogen carbonate is dissolved. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and sterilized at 129 ° C. for 7 minutes.
Comparative Example 4
The activated carbon treatment liquid obtained in the same manner as in Comparative Example 3 is mixed at the blending ratio shown in Table 1, and after adding auxiliary materials such as sugar and milk, the pH is adjusted with an aqueous solution in which sodium bicarbonate is dissolved. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and sterilized at 129 ° C. for 7 minutes.
Comparative Example 5
SV20 [1 / volume [m 3 ] / flow rate in a column packed with 50% activated carbon by weight with respect to Brix of the extract obtained from coffee beans with an extremely low roasting degree (L value 50) [ m 3 / hr]]. The coffee extract was treated. About the obtained activated carbon processing liquid, after mix | blending auxiliary materials, such as sugar and milk, pH adjustment is carried out with the aqueous solution which melt | dissolved sodium hydrogencarbonate. And it diluted with ion-exchange water. Thereafter, this solution was heated to 65 ° C. and passed through a homogenizer. Next, the mixture was heated to 75 ° C., filled into a 190 g can container, sealed, and sterilized at 129 ° C. for 7 minutes.

Figure 2008199950
Figure 2008199950

Figure 2008199950
Figure 2008199950

*1 コーヒー感の評価は、パネラー5人で官能評価した。
1;コーヒー感が強い
2;コーヒー感がやや強い
3;どちらとも言えない
4;コーヒー感がやや弱い
5;コーヒー感が弱い
*2 加温保存(55℃、1月)後の劣化風味の評価は、パネラー5人で官能評価した(劣化風味とは保存後に発生する金属臭及びそれに準ずる味)。
1;劣化風味が感じられない
2;極わずかに劣化風味が感じられる
3;わずかに劣化風味が感じられる
4;劣化風味がやや強く感じられる
5;劣化風味を強く感じる
*3 加温保存(55℃、1月)後の安定性については、目視判定を行った。
1;沈殿が無い
2;極僅かに沈殿がある
3;僅かに沈殿がある
4;沈殿がある
5;沈殿が多量にある
* 1 The feeling of coffee was sensory evaluated by five panelists.
1; Strong coffee feeling 2; Strong coffee feeling 3; Neither can be said 4; Coffee feeling is slightly weak 5; Coffee feeling is weak
* 2 Deterioration flavor after warming storage (55 ° C, January) was sensory evaluated by five panelists (deterioration flavor is a metal odor generated after storage and a taste similar to it).
1; Degraded flavor is not felt 2; Degraded flavor is felt slightly 3; Degraded flavor is felt slightly 4; Degraded flavor is felt slightly intense 5; Degraded flavor is felt strongly
* 3 Visual determination was made for stability after warming storage (55 ° C., January).
1; No precipitation 2; Slight precipitation 3; Slight precipitation 4; Precipitation 5;

Claims (6)

(A)クロロゲン酸類濃度0.14〜0.5質量%であり、
(B)クロロゲン酸類/タンニン0.6〜0.97質量比率であり、
(C)ジクロロゲン酸類/クロロゲン酸類0.06〜0.13質量比率であり、かつ、
(D)キナ酸の含有量が0.021〜0.2g/100gである
加熱殺菌処理を施した容器詰ミルクコーヒー飲料。
(A) The chlorogenic acid concentration is 0.14-0.5% by mass,
(B) Chlorogenic acids / tannin 0.6 to 0.97 mass ratio,
(C) dichlorogenic acids / chlorogenic acids 0.06 to 0.13 mass ratio, and
(D) Containerized milk coffee beverage subjected to heat sterilization treatment with a quinic acid content of 0.021 to 0.2 g / 100 g.
容器詰ミルクコーヒー飲料が缶入りである請求項1記載の容器詰ミルクコーヒー飲料。   2. The packaged milk coffee beverage according to claim 1, wherein the packaged milk coffee beverage is in a can. ミルクコーヒーの殺菌温度が123℃以上である請求項1又は2の何れか1項記載の容器詰ミルクコーヒー飲料。   The sterilization temperature of milk coffee is 123 degreeC or more, The container-packed milk coffee drink of any one of Claim 1 or 2. コーヒー抽出液を活性炭処理した請求項1〜3の何れか1項記載の容器詰ミルクコーヒー飲料。   The container-packed milk coffee beverage according to any one of claims 1 to 3, wherein the coffee extract is treated with activated carbon. L60以下の焙煎コーヒー豆を二種以上使用して、コーヒー飲料を抽出した請求項1〜4の何れか1項記載の容器詰ミルクコーヒー飲料。   The packaged milk coffee beverage according to any one of claims 1 to 4, wherein two or more roasted coffee beans of L60 or less are used to extract a coffee beverage. 乳成分を容器詰ミルクコーヒー飲料中に乳固形分換算で0.1〜10質量%含有する請求項1〜6の何れか1項記載の容器詰ミルクコーヒー飲料。   The packaged milk coffee beverage according to any one of claims 1 to 6, wherein the milk component is contained in the packaged milk coffee beverage in an amount of 0.1 to 10% by mass in terms of milk solid content.
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