JP2004313124A - Tea extract solution - Google Patents

Tea extract solution Download PDF

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Publication number
JP2004313124A
JP2004313124A JP2003114434A JP2003114434A JP2004313124A JP 2004313124 A JP2004313124 A JP 2004313124A JP 2003114434 A JP2003114434 A JP 2003114434A JP 2003114434 A JP2003114434 A JP 2003114434A JP 2004313124 A JP2004313124 A JP 2004313124A
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JP
Japan
Prior art keywords
tea extract
cellulose
precipitation
extract solution
black tea
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JP2003114434A
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Japanese (ja)
Inventor
Mitsuyo Akimoto
光代 秋元
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Asahi Kasei Chemicals Corp
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Asahi Kasei Chemicals Corp
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Priority to JP2003114434A priority Critical patent/JP2004313124A/en
Publication of JP2004313124A publication Critical patent/JP2004313124A/en
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Abstract

<P>PROBLEM TO BE SOLVED: To provide tea extract solution where coagulation of insoluble components contained in tea extract solution is suppressed and a precipitation phenomenon is mitigated, and redispersibility of the precipitation is improved without increasing viscosity of the extract. <P>SOLUTION: The tea extract solution comprises a dispersible cellulose complex containing micro cellulose and a hydrophilic polymer so as to suppress coagulation of insoluble components existing in the tea extract solution, mitigate the precipitation phenomenon and improve redispersibility of the precipitation. <P>COPYRIGHT: (C)2005,JPO&amp;NCIPI

Description

【0001】
【発明の属する技術分野】
本発明は希釈して飲料に供するための原料である茶類抽出液に関する。
【0002】
【従来の技術】
紅茶、緑茶、ウーロン茶等の茶類抽出液は茶葉を熱水抽出することによって得られるものであり、この茶類抽出液にはタンニン、カフェイン、たん白質、多糖類、アミノ酸類等が含まれる。ところが温度変化や経時変化等により茶類抽出液中のタンニンがたん白質や多糖類等と不溶性成分を形成し凝集することによって、沈殿が発生する現象が起こる。特に希釈して飲料に供するような高濃度の茶類抽出液ほどこれらの現象は発生しやすい傾向にある。このような不溶性成分の沈殿は飲料としての見栄えを損ない、商品価値を著しく低下させるので問題であった。
【0003】
濾過や遠心分離等により不溶性成分の沈殿を除去することは技術的に可能であるが、タンニン、たん白質、多糖類等の一部が除去されて茶本来の風味が損なわれてしまう。またタンニンの効果として知られている抗酸化作用、抗菌作用、腸内細菌の改善、消臭作用、活性酸素消去作用、コレステロール上昇抑制作用、血糖上昇抑制作用、血圧上昇抑制作用、抗アレルギー作用等の効果も低下する。
不溶性成分を除去することなく沈殿発生を防止する方法として、茶類抽出液にカラギーナンを添加し沈殿発生を防止する方法(特許文献1)が提案されている。しかしながらカラギーナンのような増粘安定剤を添加する方法は、条件によっては顕著な増粘傾向を示すことがあった。
【0004】
【特許文献1】
特開2000−316475号公報
【0005】
【発明が解決しようとする課題】
本発明は茶類抽出液にセルロース複合体を含有させることによって、粘度を上げることなく、茶類抽出液に含まれる不溶性成分の凝集が抑制されるとともに、沈殿現象が緩和され、沈殿の再分散性が改善された茶類抽出液を提供することを目的とする。
【0006】
【課題を解決するための手段】
本発明は茶類抽出液に含まれる不溶性成分の凝集を抑制するとともに、沈殿現象を緩和し、沈殿の再分散性が改善され、且つ低粘度で口当たりの良い茶類抽出液を提供するために鋭意研究を重ねた結果、特定のセルロース複合体を配合することにより課題を解決できることを見出し、この知見に基づいて本発明をなすに至った。すなわち本発明は、すくなくとも、微細セルロースと親水性高分子からなるセルロース複合体を含有することを特徴とする茶類抽出液である。
【0007】
【発明の実施の形態】
以下、本発明について詳細に説明する。本発明に使用されるセルロース複合体とは、すくなくとも微細セルロース20〜98質量%と親水性高分子2〜80質量%を含む組成物であり、水等を媒体として安定な懸濁液をあたえるもので、たとえば、水中で機械的に攪拌すると、後述の方法で測定した場合に平均粒径20μm以下、好ましくは10μm以下の微細セルロース粒子に分散する。本発明の分散性のセルロース複合体としては公知のものを使用することが可能であり、例えば特公昭40−14174号公報、特公昭62−43661号公報、特開平6−335365号公報に記載のものが使用できる。
【0008】
本発明で用いられる分散性のセルロース複合体は、木材パルプ、精製リンター、穀物又は果実由来の食物繊維等のセルロース系素材を酸加水分解、アルカリ酸化分解、爆砕、酵素分解等により解重合処理したのち、親水性高分子と混合して湿式共磨砕して乾燥することにより得られる。またセルロース系素材を解重合処理した後、磨砕して得られた微細セルロースに親水性高分子を均一に混合して均質なスラリーとし、これを乾燥する方法で調製しても良い。
【0009】
本発明で使用される親水性高分子とは、水あるいは冷水中で膨潤、ゲル化、溶解するような水との親和性が高い高分子を意味する。その例としてはアラビアガム、 アラビノガラクタン、アルギン酸およびその塩、カードラン、ガッティーガム、カラギーナン、カラヤガム、寒天、キサンタンガム、グアガム、酵素分解グアガム、クインスシードガム、ジェランガム、ゼラチン、タマリンドシードガム、難消化性デキストリン、トラガントガム、ファーセラン、プルラン、ペクチン、ローカストビーンガム、カルボキシメチルセルロースナトリウム等がある。
これら親水性高分子は単独で使用しても良いし複数を選択して使用しても良い。親水性高分子として好ましいのはカラギーナン、カラヤガム、キサンタンガム、ジェランガム、難消化性デキストリン、ペクチン、カルボキシメチルセルロースナトリウムである。特に好ましいのはカラヤガム、キサンタンガム、難消化性デキストリン、カルボキシメチルセルロースナトリウムである。
【0010】
また必要に応じ微細セルロースと親水性高分子に加えて、親水性物質がセルロース複合体に含まれていても良い。親水性物質とは、冷水への溶解性が高く、粘性を殆どもたらさない25℃で固体状の有機物であり、澱粉加水分解物、デキストリン類、ショ糖、ブドウ糖、果糖、乳糖、麦芽糖、異性化糖、カップリングシュガー、パラチノース、ネオシュガー、還元澱粉糖化飴、キシロース、ソルボース、ラクツロース、ポリデキストロース等の水溶性糖類、マルチトール、マンニトール、キシリトール、ソルビトール等の糖アルコール類等が挙げられる。好ましくは、澱粉加水分解物、デキストリン類、ブドウ糖、果糖、庶糖、乳糖、麦芽糖、ポリデキストロース、マンニトール、ソルビトールである。これらの親水性物質は単独で使用しても良いし複数を使用しても良い。さらにセルロース複合体の分散を妨げなければ、微細セルロース、親水性高分子、親水性物質以外に、油脂類、乳化剤等のその他成分を配合することは自由である。
【0011】
本発明の茶類抽出液における分散性のセルロース複合体の配合量は、0.01〜1.0質量%が好ましい。さらに好ましくは0.1〜0.8質量%である。これら分散性のセルロース複合体は単独で使用しても良いし、同時に複数のセルロース複合体を使用しても良い。例えば同時に複数のセルロース複合体を使用する場合、微細セルロースと天然由来親水性高分子を含むセルロース複合体と、微細セルロースとカルボキシメチルセルロースナトリウムを含むセルロース複合体を組み合わせて使用しても良い。
【0012】
本発明の茶類抽出液の濃度は特に限定されないが、たとえば、1.2〜10倍の希釈率で希釈することによって飲料として供される程度の濃度のものである。
また抽出に使用する茶葉の種類としては、紅茶、緑茶、ウーロン茶、煎茶、白茶、テン茶、プーアル茶、グァバ茶、ウコン茶、ハーブティー等が使用できる。
本発明の茶類抽出液の製造方法は、まず茶葉を熱水抽出するか又は熱水中で茶葉を煮出すことにより茶類抽出液を得るものである。また必要に応じてこの抽出液を濃縮しても良い。
【0013】
上記、えられた茶類抽出液にセルロース複合体を分散・混合させることにより、本発明の茶類抽出液をえることができる。タンニンがたん白質や多糖類等と形成した不溶性成分を一旦溶解させるために、分散時の液温は60℃以上であることが好ましい。また分散工程でpH調整剤、増粘剤、安定剤、乳化剤、消泡剤、発泡剤、牛乳、クリーム、全脂粉乳、脱脂粉乳、練乳、豆乳、糖類、塩類、香料、色素、酸味料、油脂類、たん白質、果汁、野菜汁等を添加することは特に制限されない。
【0014】
分散液の分散処理はマントンゴーリン型ホモジナイザーのような高圧ホモジナイザーを使用して行うが、処理圧力は5MPa以上であることが好ましい。特に好ましくは15MPa以上である。また必要に応じて超高圧ホモジナイザーを使用しても良い。市販の超高圧ホモジナイザーの例としては、ナノマイザー〔ナノマイザー(株)製〕やマイクロフルイダイザー〔Microfluidics社製〕がある。この処理は必要に応じて複数回実施しても良い。
このようにしてえられた、本発明の茶類抽出法を殺菌処理する方法としては、HTST殺菌法、UHT殺菌法、レトルト殺菌法、ホットパック殺菌法等があるが、必要に応じて適した殺菌法を選択する。
【0015】
本願発明の茶類抽出液は、たとえば、紙パック、テトラパック、PET容器、缶、ビン等に充填され、冷蔵又は室温で流通、保存される。充填された茶類抽出液は、一般家庭、飲食店等において、茶類抽出液を1.2〜10倍の希釈率で希釈することによって飲料として供される。希釈のために用いられる液体としては、水、牛乳、豆乳、果汁、野菜汁等があり、その温度はとくに制限されない。この時にその他の物質、例えば糖類、塩類、クリーム、全脂粉乳、脱脂粉乳、油脂類、たん白類を加えることは自由である。
【0016】
次に実施例によって本発明をさらに詳細に説明する。なお本願発明にかかる物質の諸物性の評価は以下の手法に拠った。
(a)分散粒子平均粒径の測定:固形分換算で3gの乾燥セルロース複合体サンプルに純水を加えて全量を300gとし、エクセルオートホモジナイザー〔日本精機(株)製〕にて15000rpmで5分間分散させる。この分散液をレーザー回折式粒度分布測定装置〔堀場製作所(株)製 LA−910〕を用いて、1分間超音波分散した後、相対屈折率1.20で測定した時の積算体積50%の粒径を平均粒径とした。
(b)茶類抽出液粘度測定:製造後5℃及び37℃中で、7日間及び31日間保存した後に、B形粘度計〔東京計器(株)製〕、BLアダプター、ローター回転数60rpmで測定した。
【0017】
(c)茶類抽出液中沈殿の目視観察:製造後5℃及び37℃中で、7日間及び31日間保存した後に、容器底面部に沈積した不溶性成分の沈殿を目視観察し以下のように評価した。
◎:容器底部に沈殿無し。
○:容器底部に少量の沈殿が認められる。
△:容器底部に沈殿が認められる。
×:容器底部に密で固着した沈殿が認められる。
【0018】
(d)茶類抽出液中不溶性成分の凝集状態:製造後5℃中で31日間保存した後に、それぞれの容器底部から不溶性成分をスポイトで採取して光学顕微鏡で観察した。観察倍率は40倍とし以下のように評価した。
◎:不溶性成分の凝集無し。(10μm以上の凝集物が無い。)
○:不溶性成分の弱い凝集有り。(10μm以上、20μm未満の小さい凝集物がわずかに存在するものの、20μm以上の大きな凝集物は無い。)
×:不溶性成分の強い凝集有り。(20μm以上の大きな凝集物が複数存在する。)
【0019】
(e)再分散回数:製造後5℃及び37℃中で、7日間及び31日間保存した後に再分散回数を数えた。再分散回数とは保存高濃度紅茶抽出液が入った200mLガラス製容器を倒立して元に戻す操作を1回と数え、この倒立と元に戻す操作の繰り返しによって容器底部に沈積した不溶性成分の沈殿が解消されるまでに要した回数のことである。
本発明を実施例に基づいて説明する。
【0020】
[実施例1]
(1)紅茶抽出液の調製:沸騰水2000g中に市販紅茶葉160gを添加し、5分間煮出した後、液温を70℃以上に保ちながら紅茶葉を濾別することによって得た。この紅茶抽出液の濃度は、通常飲料として供されるものの4倍の濃度である。
(2)セルロース複合体Aの調製:市販DPパルプ(平均重合度850)を裁断後、7%塩酸中で105℃、20分間加水分解処理を行い、純水にて濾過洗浄し、ウェットケークを得た。このウェットケークに、セルロース/カラヤガム/デキストリン=80/10/10の比率となるようにカラヤガムとデキストリンを配合し、ニーダーにて練合・磨砕を行った。次いで手でもみほぐしてから熱風乾燥し、ハンマーミルにて粉砕することにより、セルロース複合体Aを得た。前記(a)の手法により測定した、セルロース複合体Aの分散粒子平均粒径は、7.5μmであった。
【0021】
(3)セルロース複合体処理紅茶抽出液の調製:(1)で得られた紅茶抽出液1996gを約70℃に加温し、セルロース複合体Aを4g添加し、液温を保ちながら約10分間プロペラ攪拌して分散させた。続いてマントンゴーリン型ホモジナイザーを用いて圧力19.6MPaで分散液を処理し、次にHTST殺菌機を用いて135℃で30秒間殺菌処理して、セルロース複合体を含有する紅茶抽出液を得た。この紅茶抽出液を200mLガラス製容器に分注し、容器を10回倒立した後、5℃及び37℃で31日間保存した。
(4)茶類抽出液の評価:(3)で調製した、紅茶抽出液を、前記(b)〜(e)の手法により物性評価をおこなった。結果を表1、表2、表3、表4に示す。
【0022】
[実施例2]
(1)セルロース複合体Bの調製:実施例1で調製したウェットケークに、微細セルロース/カルボキシメチルセルロースナトリウムの比率が89/11となるようにカルボキシメチルセルロースナトリウムを加え、ニーダーにて練合・磨砕を行った。次いで手でもみほぐしてから熱風乾燥し、ハンマーミルにて粉砕することにより、セルロース複合体Bを得た。前記(a)の手法により測定した、セルロース複合体Bの分散粒子平均粒径は、8.1μmであった。
【0023】
(2)セルロース複合体Cの調製:実施例1で調製したウェットケークに純水を加え、セルロース系素材の解重合処理物が固形分換算で10質量%になるように水分散液を調製した。これを超高圧ホモジナイザーで、127.4MPaの圧力で2回破砕処理を行い、ペースト状の微細セルロースを得た。このペーストに微細セルロース/キサンタンガム/デキストリンの比率が75/5/20となるようにキサンタンガムとデキストリンを配合し、純水を加えて、総固形分濃度が7質量%の分散液を調製した。この分散液を平滑なアルミニウム板上に約3mmの厚さで伸展し、熱風乾燥機を使用して80℃で60分間乾燥し、得られたフィルム状物を手でもみほぐし、鱗片状のセルロース複合体Cを得た。前記(a)の手法により測定した、セルロース複合体Cの分散粒子平均粒径は、3.2μmであった。
【0024】
(3)セルロース複合体処理紅茶抽出液の調製:実施例1と同様に調整した紅茶抽出液1996gを約70℃に加温し、1.8gのセルロース複合体Bと2.2gのセルロース複合体Cを添加し、液温を保ちながら約10分間プロペラ攪拌して分散させた。続いてマントンゴーリン型ホモジナイザーを用いて圧力19.6MPaで分散液を処理し、次にHTST殺菌機を用いて135℃で30秒間殺菌処理して、セルロース複合体を含有する紅茶抽出液を得た。この紅茶抽出液を200mLガラス製容器に分注し、容器を10回倒立した後、5℃及び37℃で31日間保存した。
(4)茶類抽出液の評価:(3)で調製した、紅茶抽出液を、前記(b)〜(e)の手法により物性評価をおこなった。結果を表1、表2、表3、表4に示す。
【0025】
[比較例1]
(1)紅茶抽出液の調製:実施例1と同様に調整した紅茶抽出液2000gを約70℃に加温し、液温を保ちながら約10分間プロペラ攪拌した。続いてマントンゴーリン型ホモジナイザーを用いて圧力19.6MPaで分散液を処理し、次にHTST殺菌機を用いて135℃で30秒間殺菌処理して紅茶抽出液を得た。この紅茶抽出液を200mLガラス製容器に分注し、容器を10回倒立した後、5℃及び37℃で31日間保存した。
(2)茶類抽出液の評価:(1)で調製した、紅茶抽出液を、前記(b)〜(e)の手法により物性評価をおこなった。結果を表1、表2、表3、表4に示す。
【0026】
[比較例2]
(1)紅茶抽出液の調製:実施例1と同様に調整した紅茶抽出液1999gを約70℃に加温し、1.0gのカラギーナンを添加し、液温を保ちながら約10分間プロペラ攪拌して分散させた。続いてマントンゴーリン型ホモジナイザーを用いて圧力19.6MPaで分散液を処理し、次にHTST殺菌機を用いて135℃で30秒間殺菌処理して、セルロース複合体を含有する紅茶抽出液を得た。この紅茶抽出液を200mLガラス製容器に分注し、容器を10回倒立した後、5℃及び37℃で31日間保存した。
(2)茶類抽出液の評価:(1)で調製した、紅茶抽出液を、前記(b)〜(e)の手法により物性評価をおこなった。結果を表1、表2、表3、表4に示す。
【0027】
【表1】

Figure 2004313124
【0028】
【表2】
Figure 2004313124
【0029】
【表3】
Figure 2004313124
【0030】
【表4】
Figure 2004313124
【0031】
【発明の効果】
茶類抽出液にセルロース複合体を含有させることによって、粘度を上げることなく、茶類抽出液に含まれる不溶性成分の凝集を抑制することができる。不溶性成分の凝集抑制により、密で固着した沈殿物ではなく疎な沈降層を形成させることができるので、沈殿の再分散性を改善できる。またセルロース複合体添加による顕著な増粘は無いので、喉ごしの良い茶類飲料を提供することができる。[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to a tea extract which is a raw material for use in a beverage after dilution.
[0002]
[Prior art]
Tea extracts such as black tea, green tea, and oolong tea are obtained by extracting tea leaves with hot water, and this tea extract contains tannins, caffeine, proteins, polysaccharides, amino acids, and the like. . However, tannins in the tea extract form insoluble components with proteins, polysaccharides, and the like due to changes in temperature, changes over time, and the like, causing a phenomenon in which precipitation occurs. In particular, these phenomena tend to be more likely to occur in a tea extract having a higher concentration, such as a diluted tea beverage. Such precipitation of insoluble components is a problem because it impairs the appearance of the beverage and significantly lowers the commercial value.
[0003]
Although it is technically possible to remove precipitates of insoluble components by filtration, centrifugation, or the like, tannins, proteins, polysaccharides, and the like are partially removed, thereby impairing the original flavor of tea. Also known as the effects of tannin, antioxidant action, antibacterial action, improvement of intestinal bacteria, deodorant action, active oxygen scavenging action, cholesterol rise suppression action, blood sugar rise suppression action, blood pressure rise suppression action, antiallergic action, etc. Effect is also reduced.
As a method of preventing the occurrence of precipitation without removing insoluble components, a method of adding carrageenan to a tea extract to prevent the occurrence of precipitation (Patent Document 1) has been proposed. However, the method of adding a thickening stabilizer such as carrageenan sometimes shows a remarkable thickening tendency depending on conditions.
[0004]
[Patent Document 1]
JP 2000-316475 A
[Problems to be solved by the invention]
The present invention includes a cellulose complex in a tea extract, suppressing the aggregation of insoluble components contained in the tea extract, increasing the viscosity, reducing the sedimentation phenomenon, and redispersing the precipitate without increasing the viscosity. An object of the present invention is to provide a tea extract having improved properties.
[0006]
[Means for Solving the Problems]
The present invention suppresses the aggregation of the insoluble components contained in the tea extract, alleviates the precipitation phenomenon, improves the redispersibility of the precipitate, and provides a low-viscosity and tasteful tea extract. As a result of intensive studies, they have found that the problem can be solved by blending a specific cellulose composite, and have accomplished the present invention based on this finding. That is, the present invention is a tea extract characterized by containing at least a cellulose composite comprising fine cellulose and a hydrophilic polymer.
[0007]
BEST MODE FOR CARRYING OUT THE INVENTION
Hereinafter, the present invention will be described in detail. The cellulose composite used in the present invention is a composition containing at least 20 to 98% by mass of fine cellulose and 2 to 80% by mass of a hydrophilic polymer, and gives a stable suspension using water or the like as a medium. For example, when mechanically stirred in water, the particles are dispersed in fine cellulose particles having an average particle size of 20 μm or less, preferably 10 μm or less, as measured by the method described below. As the dispersible cellulose composite of the present invention, known ones can be used, for example, those described in JP-B-40-14174, JP-B-62-43661, and JP-A-6-335365. Things can be used.
[0008]
The dispersible cellulose composite used in the present invention was obtained by subjecting a cellulose-based material such as wood pulp, refined linter, grain or fruit-derived dietary fiber to depolymerization treatment by acid hydrolysis, alkali oxidative decomposition, explosion, enzymatic decomposition, or the like. Thereafter, it is obtained by mixing with a hydrophilic polymer, wet co-milling and drying. Alternatively, after a cellulose-based material is depolymerized, a hydrophilic polymer may be uniformly mixed with fine cellulose obtained by grinding to form a homogeneous slurry, and the slurry may be dried.
[0009]
The hydrophilic polymer used in the present invention means a polymer having a high affinity for water, which swells, gels and dissolves in water or cold water. Examples include gum arabic, arabinogalactan, alginic acid and its salts, curdlan, guttie gum, carrageenan, karaya gum, agar, xanthan gum, guar gum, enzymatically degraded guar gum, quince seed gum, gellan gum, gelatin, tamarind seed gum, indigestible Dextrin, tragacanth, furcellane, pullulan, pectin, locust bean gum, sodium carboxymethylcellulose and the like.
These hydrophilic polymers may be used alone or a plurality of them may be selected and used. Preferred as the hydrophilic polymer are carrageenan, karaya gum, xanthan gum, gellan gum, indigestible dextrin, pectin, and sodium carboxymethylcellulose. Particularly preferred are karaya gum, xanthan gum, resistant dextrin and sodium carboxymethylcellulose.
[0010]
If necessary, a hydrophilic substance may be contained in the cellulose composite in addition to the fine cellulose and the hydrophilic polymer. Hydrophilic substances are organic substances that are highly soluble in cold water and are hardly viscous and are solid at 25 ° C., starch hydrolysates, dextrins, sucrose, glucose, fructose, lactose, maltose, Sugars, coupling sugars, palatinose, neosugar, reduced starch saccharified candy, water-soluble sugars such as xylose, sorbose, lactulose and polydextrose, and sugar alcohols such as maltitol, mannitol, xylitol and sorbitol. Preferred are starch hydrolysates, dextrins, glucose, fructose, sucrose, lactose, maltose, polydextrose, mannitol and sorbitol. These hydrophilic substances may be used alone or in combination. Further, other components such as oils and fats, emulsifiers and the like can be freely added in addition to the fine cellulose, the hydrophilic polymer and the hydrophilic substance as long as the dispersion of the cellulose composite is not hindered.
[0011]
The amount of the dispersible cellulose complex in the tea extract of the present invention is preferably 0.01 to 1.0% by mass. More preferably, it is 0.1 to 0.8% by mass. These dispersible cellulose composites may be used alone, or a plurality of cellulose composites may be used at the same time. For example, when a plurality of cellulose composites are used at the same time, a cellulose composite containing fine cellulose and a naturally derived hydrophilic polymer and a cellulose composite containing fine cellulose and sodium carboxymethylcellulose may be used in combination.
[0012]
The concentration of the tea extract of the present invention is not particularly limited, but is, for example, a concentration such that the tea extract is provided as a beverage by being diluted at a dilution ratio of 1.2 to 10 times.
As the type of tea leaves used for extraction, black tea, green tea, oolong tea, sencha, white tea, ten tea, puer tea, guava tea, turmeric tea, herbal tea, and the like can be used.
In the method for producing a tea extract of the present invention, first, tea leaves are extracted with hot water or tea leaves are boiled in hot water to obtain a tea extract. This extract may be concentrated if necessary.
[0013]
The tea extract of the present invention can be obtained by dispersing and mixing the cellulose complex in the obtained tea extract. The liquid temperature at the time of dispersion is preferably 60 ° C. or higher in order to temporarily dissolve the insoluble components formed by tannin with proteins and polysaccharides. In the dispersion step, a pH adjuster, a thickener, a stabilizer, an emulsifier, an antifoaming agent, a foaming agent, milk, cream, whole milk powder, skim milk powder, condensed milk, soy milk, sugars, salts, flavors, pigments, acidulants, Addition of fats and oils, protein, fruit juice, vegetable juice and the like is not particularly limited.
[0014]
The dispersion treatment of the dispersion is performed using a high-pressure homogenizer such as a Manton-Gaulin type homogenizer, and the treatment pressure is preferably 5 MPa or more. Particularly preferably, it is 15 MPa or more. If necessary, an ultra-high pressure homogenizer may be used. Examples of commercially available ultrahigh-pressure homogenizers include a Nanomizer (manufactured by Nanomizer Co., Ltd.) and a microfluidizer (manufactured by Microfluidics). This processing may be performed a plurality of times as necessary.
As a method for sterilizing the tea extraction method of the present invention thus obtained, there are HTST sterilization, UHT sterilization, retort sterilization, hot pack sterilization, and the like. Choose a sterilization method.
[0015]
The tea extract of the present invention is filled in, for example, a paper pack, a tetrapack, a PET container, a can, a bottle, and the like, and is refrigerated or distributed and stored at room temperature. The filled tea extract is used as a beverage in ordinary households, restaurants and the like by diluting the tea extract at a dilution ratio of 1.2 to 10 times. Liquids used for dilution include water, milk, soy milk, fruit juice, vegetable juice, and the like, and the temperature is not particularly limited. At this time, other substances such as sugars, salts, cream, whole milk powder, skim milk powder, fats and oils, and proteins can be freely added.
[0016]
Next, the present invention will be described in more detail by way of examples. The evaluation of various physical properties of the substance according to the present invention was based on the following methods.
(A) Measurement of average particle diameter of dispersed particles: 3 g of a dried cellulose composite sample in terms of solid content was added with pure water to make the total amount 300 g, and then 5 minutes at 15000 rpm using an Excel Auto Homogenizer (manufactured by Nippon Seiki Co., Ltd.). Disperse. This dispersion was subjected to ultrasonic dispersion for 1 minute using a laser diffraction particle size distribution analyzer [LA-910, manufactured by Horiba, Ltd.], and then the integrated volume of 50% when measured at a relative refractive index of 1.20 was obtained. The particle size was taken as the average particle size.
(B) Measurement of viscosity of tea extract: After storage at 5 ° C. and 37 ° C. for 7 days and 31 days, a B-type viscometer (manufactured by Tokyo Keiki Co., Ltd.), a BL adapter, and a rotor rotation speed of 60 rpm. It was measured.
[0017]
(C) Visual observation of the precipitate in the tea extract: After storage at 5 ° C. and 37 ° C. for 7 days and 31 days after the production, the precipitate of the insoluble component deposited on the bottom of the container was visually observed as follows. evaluated.
:: No precipitation at the bottom of the container.
:: A small amount of precipitation is observed at the bottom of the container.
Δ: Precipitation is observed at the bottom of the container.
X: A densely adhered precipitate is observed at the bottom of the container.
[0018]
(D) Aggregation state of insoluble components in tea extract: After storage at 5 ° C. for 31 days after production, insoluble components were collected from the bottom of each container with a dropper and observed with an optical microscope. The observation magnification was 40 times and evaluated as follows.
A: No aggregation of insoluble components. (There is no aggregate of 10 μm or more.)
:: Weak aggregation of insoluble components. (There are few small aggregates of 10 μm or more and less than 20 μm, but no large aggregates of 20 μm or more.)
X: Strong aggregation of insoluble components. (A plurality of large aggregates of 20 μm or more exist.)
[0019]
(E) Number of redispersions: After storage at 5 ° C and 37 ° C for 7 days and 31 days, the number of redispersions was counted. The number of times of redispersion is defined as counting the operation of inverting and returning the 200 mL glass container containing the preserved high-concentration black tea extract to one time, and repeating the operation of inverting and returning the insoluble component deposited on the bottom of the container. This is the number of times required for the precipitation to be resolved.
The present invention will be described based on examples.
[0020]
[Example 1]
(1) Preparation of black tea extract: 160 g of commercially available black tea leaves were added to 2000 g of boiling water, and after boiling for 5 minutes, the black tea leaves were obtained by filtering the black tea leaves while maintaining the liquid temperature at 70 ° C. or higher. The concentration of this black tea extract is four times that of what is usually served as a beverage.
(2) Preparation of cellulose composite A: Commercial DP pulp (average degree of polymerization: 850) was cut, hydrolyzed at 105 ° C. for 20 minutes in 7% hydrochloric acid, filtered and washed with pure water, and wet cake was removed. Obtained. Karaya gum and dextrin were blended with the wet cake in a ratio of cellulose / karaya gum / dextrin = 80/10/10, and kneaded and milled in a kneader. Next, the mixture was loosened by hand, dried with hot air, and pulverized with a hammer mill to obtain a cellulose composite A. The average particle size of the dispersed particles of the cellulose composite A measured by the method (a) was 7.5 μm.
[0021]
(3) Preparation of black tea extract treated with cellulose complex: 1996 g of the black tea extract obtained in (1) was heated to about 70 ° C., 4 g of cellulose complex A was added, and about 10 minutes while maintaining the liquid temperature The mixture was dispersed by stirring with a propeller. Subsequently, the dispersion was treated with a Menton-Gaulin type homogenizer at a pressure of 19.6 MPa, and then sterilized with an HTST sterilizer at 135 ° C. for 30 seconds to obtain a black tea extract containing a cellulose complex. . This black tea extract was dispensed into a 200 mL glass container, the container was inverted 10 times, and then stored at 5 ° C. and 37 ° C. for 31 days.
(4) Evaluation of tea extract: The black tea extract prepared in (3) was evaluated for physical properties by the methods (b) to (e) described above. The results are shown in Tables 1, 2, 3 and 4.
[0022]
[Example 2]
(1) Preparation of Cellulose Composite B: To the wet cake prepared in Example 1, sodium carboxymethylcellulose was added so that the ratio of fine cellulose / sodium carboxymethylcellulose was 89/11, and kneaded and milled in a kneader. Was done. Next, the mixture was loosened by hand, dried with hot air, and pulverized with a hammer mill to obtain a cellulose composite B. The average particle size of the dispersed particles of the cellulose composite B measured by the method (a) was 8.1 μm.
[0023]
(2) Preparation of Cellulose Composite C: Pure water was added to the wet cake prepared in Example 1, and an aqueous dispersion was prepared so that the depolymerized product of the cellulosic material was 10% by mass in terms of solid content. . This was subjected to a crushing treatment twice with an ultrahigh pressure homogenizer at a pressure of 127.4 MPa to obtain paste-like fine cellulose. Xanthan gum and dextrin were blended with this paste so that the ratio of fine cellulose / xanthan gum / dextrin was 75/5/20, and pure water was added to prepare a dispersion having a total solid content concentration of 7% by mass. This dispersion is spread on a smooth aluminum plate to a thickness of about 3 mm, and dried at 80 ° C. for 60 minutes using a hot-air drier. Complex C was obtained. The average particle size of the dispersed particles of the cellulose composite C measured by the method (a) was 3.2 μm.
[0024]
(3) Preparation of cellulose complex-treated black tea extract: 1996 g of black tea extract prepared in the same manner as in Example 1 was heated to about 70 ° C., and 1.8 g of cellulose complex B and 2.2 g of cellulose complex were obtained. C was added and dispersed by stirring with a propeller for about 10 minutes while maintaining the liquid temperature. Subsequently, the dispersion was treated with a Menton-Gaulin type homogenizer at a pressure of 19.6 MPa, and then sterilized with an HTST sterilizer at 135 ° C. for 30 seconds to obtain a black tea extract containing a cellulose complex. . This black tea extract was dispensed into a 200 mL glass container, the container was inverted 10 times, and then stored at 5 ° C. and 37 ° C. for 31 days.
(4) Evaluation of tea extract: The black tea extract prepared in (3) was evaluated for physical properties by the methods (b) to (e) described above. The results are shown in Tables 1, 2, 3 and 4.
[0025]
[Comparative Example 1]
(1) Preparation of black tea extract: 2000 g of black tea extract prepared in the same manner as in Example 1 was heated to about 70 ° C. and stirred with a propeller for about 10 minutes while maintaining the liquid temperature. Subsequently, the dispersion was treated at a pressure of 19.6 MPa using a Manton-Gaulin homogenizer, and then sterilized at 135 ° C. for 30 seconds using an HTST sterilizer to obtain a black tea extract. This black tea extract was dispensed into a 200 mL glass container, the container was inverted 10 times, and then stored at 5 ° C. and 37 ° C. for 31 days.
(2) Evaluation of tea extract: The black tea extract prepared in (1) was evaluated for physical properties by the methods (b) to (e). The results are shown in Tables 1, 2, 3 and 4.
[0026]
[Comparative Example 2]
(1) Preparation of black tea extract: 1999 g of black tea extract prepared in the same manner as in Example 1 was heated to about 70 ° C., 1.0 g of carrageenan was added, and the propeller was stirred for about 10 minutes while maintaining the liquid temperature. And dispersed. Subsequently, the dispersion was treated with a Menton-Gaulin type homogenizer at a pressure of 19.6 MPa, and then sterilized with an HTST sterilizer at 135 ° C. for 30 seconds to obtain a black tea extract containing a cellulose complex. . This black tea extract was dispensed into a 200 mL glass container, the container was inverted 10 times, and then stored at 5 ° C. and 37 ° C. for 31 days.
(2) Evaluation of tea extract: The black tea extract prepared in (1) was evaluated for physical properties by the methods (b) to (e). The results are shown in Tables 1, 2, 3 and 4.
[0027]
[Table 1]
Figure 2004313124
[0028]
[Table 2]
Figure 2004313124
[0029]
[Table 3]
Figure 2004313124
[0030]
[Table 4]
Figure 2004313124
[0031]
【The invention's effect】
By including the cellulose complex in the tea extract, it is possible to suppress aggregation of insoluble components contained in the tea extract without increasing the viscosity. By suppressing aggregation of the insoluble component, a sparse sedimentary layer can be formed instead of a dense and fixed sediment, so that the redispersibility of the sediment can be improved. In addition, since there is no remarkable thickening due to the addition of the cellulose complex, a tea beverage having a good throat can be provided.

Claims (1)

すくなくとも、微細セルロースと親水性高分子からなるセルロース複合体を含有することを特徴とする茶類抽出液。A tea extract comprising at least a cellulose composite comprising fine cellulose and a hydrophilic polymer.
JP2003114434A 2003-04-18 2003-04-18 Tea extract solution Pending JP2004313124A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006100933B4 (en) * 2006-11-01 2006-12-14 Chocolate Genie Willoughby Pty Limited Method of making a tea concentrate
WO2010097255A3 (en) * 2009-02-27 2010-10-21 Unilever Plc Beverage containing tea solids, a polymeric polyphenol, added protein and added anionic polysaccharide
KR20140075598A (en) * 2012-12-11 2014-06-19 삼성정밀화학 주식회사 Composition for complex, complex formed therefrom, and orally ingestible composition including the same
JP2015012845A (en) * 2013-07-08 2015-01-22 サントリー食品インターナショナル株式会社 Black tea syrup for dilution drink

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2006100933B4 (en) * 2006-11-01 2006-12-14 Chocolate Genie Willoughby Pty Limited Method of making a tea concentrate
WO2010097255A3 (en) * 2009-02-27 2010-10-21 Unilever Plc Beverage containing tea solids, a polymeric polyphenol, added protein and added anionic polysaccharide
KR20140075598A (en) * 2012-12-11 2014-06-19 삼성정밀화학 주식회사 Composition for complex, complex formed therefrom, and orally ingestible composition including the same
CN104870544A (en) * 2012-12-11 2015-08-26 三星精密化学株式会社 Composition for forming complex, complex formed therefrom, and composition for oral administration including said complex
EP2933290A4 (en) * 2012-12-11 2016-11-09 Lotte Fine Chemical Co Ltd Composition for forming complex, complex formed therefrom, and composition for oral administration including said complex
US9555121B2 (en) 2012-12-11 2017-01-31 Lotte Fine Chemical Co., Ltd. Composition for forming complex, complex formed therefrom, and composition for oral administration including said complex
CN104870544B (en) * 2012-12-11 2017-11-28 乐天精密化学株式会社 For the composition for forming compound, the compound being consequently formed and for the oral composition containing the compound
KR102142539B1 (en) 2012-12-11 2020-08-07 롯데정밀화학 주식회사 Composition for complex, complex formed therefrom, and orally ingestible composition including the same
JP2015012845A (en) * 2013-07-08 2015-01-22 サントリー食品インターナショナル株式会社 Black tea syrup for dilution drink

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