JPH04325060A - Thermally stable food composition - Google Patents
Thermally stable food compositionInfo
- Publication number
- JPH04325060A JPH04325060A JP3097219A JP9721991A JPH04325060A JP H04325060 A JPH04325060 A JP H04325060A JP 3097219 A JP3097219 A JP 3097219A JP 9721991 A JP9721991 A JP 9721991A JP H04325060 A JPH04325060 A JP H04325060A
- Authority
- JP
- Japan
- Prior art keywords
- food
- cellulose
- food composition
- particle size
- suspension
- 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.)
- Granted
Links
- 235000013305 food Nutrition 0.000 title claims abstract description 48
- 239000000203 mixture Substances 0.000 title claims abstract description 15
- 239000001913 cellulose Substances 0.000 claims abstract description 40
- 229920002678 cellulose Polymers 0.000 claims abstract description 40
- 239000002245 particle Substances 0.000 claims abstract description 36
- 238000010438 heat treatment Methods 0.000 claims abstract description 24
- 239000000725 suspension Substances 0.000 claims abstract description 15
- 230000001186 cumulative effect Effects 0.000 claims description 17
- 238000004945 emulsification Methods 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 7
- 230000008520 organization Effects 0.000 claims 1
- 235000003086 food stabiliser Nutrition 0.000 abstract description 5
- 239000000839 emulsion Substances 0.000 abstract description 3
- 238000007669 thermal treatment Methods 0.000 abstract 1
- 235000010980 cellulose Nutrition 0.000 description 37
- 244000299461 Theobroma cacao Species 0.000 description 9
- 235000009470 Theobroma cacao Nutrition 0.000 description 9
- 230000006378 damage Effects 0.000 description 9
- 230000007423 decrease Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000004519 manufacturing process Methods 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 7
- 238000005259 measurement Methods 0.000 description 7
- 235000014347 soups Nutrition 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 7
- 235000011850 desserts Nutrition 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 239000007900 aqueous suspension Substances 0.000 description 5
- 229920000168 Microcrystalline cellulose Polymers 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 235000019813 microcrystalline cellulose Nutrition 0.000 description 4
- 239000008108 microcrystalline cellulose Substances 0.000 description 4
- 229940016286 microcrystalline cellulose Drugs 0.000 description 4
- 238000010298 pulverizing process Methods 0.000 description 4
- 230000001954 sterilising effect Effects 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 235000013361 beverage Nutrition 0.000 description 3
- 238000004364 calculation method Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 235000019543 dairy drink Nutrition 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- -1 glycerin fatty acid esters Chemical class 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000004062 sedimentation Methods 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 230000008719 thickening Effects 0.000 description 3
- 108010073771 Soybean Proteins Proteins 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000005903 acid hydrolysis reaction Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 235000010418 carrageenan Nutrition 0.000 description 2
- 239000000679 carrageenan Substances 0.000 description 2
- 229920001525 carrageenan Polymers 0.000 description 2
- 229940113118 carrageenan Drugs 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000007884 disintegrant Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 235000015110 jellies Nutrition 0.000 description 2
- 239000008274 jelly Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229920001277 pectin Polymers 0.000 description 2
- 239000001814 pectin Substances 0.000 description 2
- 235000010987 pectin Nutrition 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 235000011962 puddings Nutrition 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000013322 soy milk Nutrition 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 235000013618 yogurt Nutrition 0.000 description 2
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical class CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 241000609240 Ambelania acida Species 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 1
- 235000017491 Bambusa tulda Nutrition 0.000 description 1
- 240000008564 Boehmeria nivea Species 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010013911 Dysgeusia Diseases 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920002148 Gellan gum Polymers 0.000 description 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
- 229920002907 Guar gum Polymers 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- 240000007472 Leucaena leucocephala Species 0.000 description 1
- 235000010643 Leucaena leucocephala Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 244000082204 Phyllostachys viridis Species 0.000 description 1
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 239000004373 Pullulan Substances 0.000 description 1
- 229920001218 Pullulan Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 241000934878 Sterculia Species 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 240000004584 Tamarindus indica Species 0.000 description 1
- 235000004298 Tamarindus indica Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000010905 bagasse Substances 0.000 description 1
- 235000015173 baked goods and baking mixes Nutrition 0.000 description 1
- 239000011425 bamboo Substances 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 235000021438 curry Nutrition 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 235000010492 gellan gum Nutrition 0.000 description 1
- 239000000216 gellan gum Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 235000009569 green tea Nutrition 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 235000015243 ice cream Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
- 239000000231 karaya gum Substances 0.000 description 1
- 229940039371 karaya gum Drugs 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000020124 milk-based beverage Nutrition 0.000 description 1
- 230000004660 morphological change Effects 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 235000019423 pullulan Nutrition 0.000 description 1
- 235000015067 sauces Nutrition 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 235000019615 sensations Nutrition 0.000 description 1
- 235000020183 skimmed milk Nutrition 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 235000019710 soybean protein Nutrition 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 235000013547 stew Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000008256 whipped cream Substances 0.000 description 1
- 235000008939 whole milk Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Landscapes
- General Preparation And Processing Of Foods (AREA)
- Seeds, Soups, And Other Foods (AREA)
- Jellies, Jams, And Syrups (AREA)
- Non-Alcoholic Beverages (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Confectionery (AREA)
- Grain Derivatives (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、熱に安定な食品組成物
に関するものである。更に詳しくは、嗜好飲料、乳性飲
料、デザート類、調理食品等加熱工程を必要とする食品
の製造に際して、積算体積50%の粒径が0.3〜6μ
m、3μm以下の粒子の積算体積の割合が25%以上、
温度上昇による見掛粘度の比が1以上の微粒化セルロー
スを添加することにより、加熱による乳化、懸濁および
組織の破壊を防止し、安定性に優れた食品組成物に関す
るものである。FIELD OF THE INVENTION This invention relates to heat-stable food compositions. More specifically, when manufacturing foods that require a heating process such as beverages, dairy drinks, desserts, and cooked foods, the particle size at 50% of the cumulative volume is 0.3 to 6μ.
m, the cumulative volume ratio of particles of 3 μm or less is 25% or more,
The present invention relates to a food composition that prevents emulsification, suspension, and tissue destruction due to heating and has excellent stability by adding micronized cellulose having an apparent viscosity ratio of 1 or more due to temperature rise.
【0002】0002
【従来の技術】一般に食品の製造においては、例えばレ
トルト食品に代表されるように加熱殺菌による保存性の
向上を目的とした加熱処理が施されることが多い。この
場合、加熱時の熱運動による組織の破壊および見掛粘度
が急激に低下することによる乳化、懸濁安定性の低下、
離水を伴う組織変化等により著しく商品価値が低下する
という問題がある。BACKGROUND OF THE INVENTION Generally, in the production of foods, heat treatment is often performed for the purpose of improving preservability by heat sterilization, as typified by retort foods. In this case, tissue destruction due to thermal movement during heating and emulsification due to a sudden decrease in apparent viscosity, decrease in suspension stability,
There is a problem in that the commercial value is significantly reduced due to structural changes accompanied by syneresis.
【0003】従来、かかる食品の乳化、懸濁安定性およ
び組織の安定性を賦与する方法として、グリセリン脂肪
酸エステル、しょ糖脂肪酸エステル等の乳化剤やカラギ
ーナン、ペクチン等の増粘安定剤を併用する方法、更に
は微結晶セルロースと分散剤、崩壊剤の複合体(市販品
アビセルRC−N81、RC−N30 旭化成工業(
株)製)を用いる方法が一般に行われている。Conventionally, methods for imparting emulsification, suspension stability and tissue stability to such foods include the combined use of emulsifiers such as glycerin fatty acid esters and sucrose fatty acid esters, and thickening stabilizers such as carrageenan and pectin; Furthermore, a complex of microcrystalline cellulose, a dispersant, and a disintegrant (commercial products Avicel RC-N81, RC-N30, Asahi Kasei Kogyo Co., Ltd.)
(manufactured by Co., Ltd.) is generally used.
【0004】0004
【発明が解決しようとする課題】しかしながら、従来の
技術には次の様な課題が残されていた。即ち、乳化剤、
増粘安定剤の使用は、加熱前には効果があるが、加熱に
よる温度上昇により急激に食品の粘度が低下し、乳化、
懸濁状態や組織の破壊により、分散粒子の沈降や離水、
油の分離といった問題が起こり、安定な食品の製造が困
難である。また乳化剤の使用はそのもの特有の味を有す
るため、食品の本来の味を損なうという欠点があり、増
粘安定剤は高い粘性を有するため口当りが重くなり、ソ
フトさ、ライト感覚が要求される食品には向かない。こ
れらの欠点を改善する方法として、微結晶セルロースと
分散剤、崩壊剤の複合体を使用する方法があるが、これ
は水不溶性であるため、加熱による粘度の低下率は低く
食品の安定性は改善されるが、微結晶セルロースの大粒
子によるザラツキ感が残ることがある。また、食品の安
定性を発揮させるためのコロイド粒子を発生させるため
には、強力な攪拌工程を必要とし、実際の使用に当たっ
ては制限を受けるという問題がある。[Problems to be Solved by the Invention] However, the following problems remain in the conventional technology. That is, emulsifiers,
The use of thickening stabilizers is effective before heating, but as the temperature rises due to heating, the viscosity of the food decreases rapidly, causing emulsification and
Due to the suspended state and destruction of the structure, sedimentation of dispersed particles and syneresis,
Problems such as oil separation occur, making it difficult to produce stable foods. In addition, the use of emulsifiers has the disadvantage of impairing the original taste of the food because it has its own unique taste.Thickening stabilizers have a high viscosity, making the mouthfeel heavy, and foods that require softness and a light sensation. Not suitable for One way to improve these drawbacks is to use a complex of microcrystalline cellulose, a dispersant, and a disintegrant, but since this is water-insoluble, the rate of viscosity reduction upon heating is low and food stability is poor. Although it is improved, a rough feeling due to the large particles of microcrystalline cellulose may remain. Furthermore, in order to generate colloidal particles to ensure food stability, a powerful stirring process is required, which poses a problem of limitations in actual use.
【0005】本発明は、これらの問題を一挙に解決し、
加熱処理による乳化や懸濁の破壊、組織の劣化を防ぎ、
かつ、ザラツキがなく、味に影響を与えない長期に安定
な食品組成物を提供するものである。[0005] The present invention solves these problems at once,
Prevents emulsification and suspension destruction and tissue deterioration caused by heat treatment,
Moreover, the present invention provides a long-term stable food composition that is free from graininess and does not affect taste.
【0006】[0006]
【課題を解決するための手段】即ち、本発明は、嗜好飲
料、乳性飲料、デザート類、調理食品等加熱工程を必要
とする食品の製造に際して、積算体積50%の粒径が0
.3〜6μm、3μm以下の粒子の積算体積割合が25
%以上、温度上昇による見掛粘度の比が1以上の微粒化
セルロースを添加することにより、加熱による乳化、懸
濁および組織の破壊を防止し、長期安定性に優れた食品
組成物に関するものである。[Means for Solving the Problems] That is, the present invention provides a method for producing foods that require a heating process, such as recreational drinks, dairy drinks, desserts, and cooked foods, such that the particle size at 50% of the cumulative volume is 0.
.. 3 to 6 μm, cumulative volume ratio of particles of 3 μm or less is 25
% or more, and the ratio of apparent viscosity due to temperature rise is 1 or more by adding micronized cellulose, which prevents emulsification, suspension and tissue destruction due to heating, and has excellent long-term stability. be.
【0007】更に本発明を詳細に説明する。本発明に用
いる微粒化セルロースとは、セルロース系素材に解重合
処理を施し、引き続き湿式粉砕することによって得られ
る。上記セルロース素材とは、例えば木材、バガス、竹
から得られるパルプ、精製リンター、綿繊維、亜麻繊維
、麻繊維、ラミー繊維等の脱リグニン後の天然セルロー
スなどである。また、上記解重合処理とは、例えば酸加
水分解、アルカリ酸化分解、酵素分解、スチームエクス
プロージョン分解、水蒸気蒸煮のうちの1つまたは2つ
以上の組合せ処理などであり、本発明の目的のためには
酸加水分解により重合度を60〜375にすることが好
ましい。また、湿式粉砕方法としては、媒体攪拌湿式粉
砕装置、ミキサー、ニーダー、エクストルーダー等、磨
砕、粉砕の機能を有する装置の1つまたは2つ以上の手
段を用いることが出来るが、効率よく微粒子化を達成さ
せるためには媒体攪拌粉砕装置(通称ビーズミルまたは
アニューラー型ミル)が適している。The present invention will be further explained in detail. The micronized cellulose used in the present invention is obtained by depolymerizing a cellulose material and subsequently wet-pulverizing it. The above-mentioned cellulose material includes, for example, pulp obtained from wood, bagasse, and bamboo, purified linter, and natural cellulose after delignification such as cotton fiber, flax fiber, hemp fiber, and ramie fiber. Further, the above-mentioned depolymerization treatment includes, for example, one or a combination of two or more of acid hydrolysis, alkali oxidative decomposition, enzymatic decomposition, steam explosion decomposition, and steam steaming. It is preferable to adjust the degree of polymerization to 60 to 375 by acid hydrolysis. In addition, as a wet pulverization method, one or more means such as a media stirring wet pulverizer, a mixer, a kneader, an extruder, etc. having the functions of grinding and pulverization can be used. In order to achieve this, a media agitation grinding device (commonly known as a bead mill or annular mill) is suitable.
【0008】以上の方法によって得られた微粒化セルロ
ースは、積算体積50%以上の粒径が0.3〜6μm、
3μm以下の粒子の積算体積割合が25%以上であり、
微粒化セルロースのペースト状および水懸濁液の温度上
昇による見掛粘度の比(例えば、3wt%濃度の水懸濁
液の20℃と80℃の粘度比η80/η20)が1以上
であること、即ち、加熱による温度上昇によって粘度の
低下が起こらないか、または上昇するという特徴を有す
る。
また、一旦温度が上昇した状態から温度を下げた場合、
粘度も回復するという熱可逆性を示す。[0008] The micronized cellulose obtained by the above method has a particle size of 0.3 to 6 μm in a cumulative volume of 50% or more;
The cumulative volume ratio of particles of 3 μm or less is 25% or more,
The ratio of the apparent viscosity due to temperature increase of the atomized cellulose paste and aqueous suspension (for example, the viscosity ratio η80/η20 at 20°C and 80°C of an aqueous suspension with a concentration of 3 wt%) is 1 or more. That is, the viscosity does not decrease or increases as the temperature increases due to heating. Also, if the temperature is lowered from a state where the temperature has risen,
It exhibits thermoreversibility in that the viscosity also recovers.
【0009】粒径の測定は本発明にとって非常に重要な
要素であるが、本発明者等は島津レーザ回折式粒度分布
測定装置(SALD−1100)を用いて、測定に供す
る懸濁液を、水性懸濁液の場合は蒸留水で、非水性懸濁
液の場合はその主たる分散媒で0.1重量%に希釈し、
装置に内蔵する超音波発進器で2次凝集を壊した状態で
測定する。Measurement of particle size is a very important element for the present invention, and the present inventors used a Shimadzu laser diffraction particle size distribution analyzer (SALD-1100) to measure the suspension to be subjected to measurement. Dilute to 0.1% by weight with distilled water in the case of an aqueous suspension, or with its main dispersion medium in the case of a non-aqueous suspension,
Measurement is performed after secondary aggregation is broken using an ultrasonic generator built into the device.
【0010】本発明での積算体積割合50%の粒径とは
、粒子全体の体積に対して積算体積が50%になる時の
粒子の球形換算直径のことである。なお、該粒度分布測
定装置での測定にあたっては、測定レンジを0.1〜4
5μに設定する。これにより、ミー(Mie)散乱理論
式(測定装置中に組み込まれている)から導き出された
散乱光強度と粒子径の関係を用いて計算されることとな
る。また、屈折率は1.7−0.2iの標準屈折率用を
選択することとし、粒度分布を求める計算方法は最小二
乗法理論を使った直接計算法を使うこととする。1つの
試料に対する測定回数は7回に指定し、測定間隔は2秒
とする。[0010] In the present invention, the particle size at a cumulative volume ratio of 50% refers to the spherical equivalent diameter of the particles when the cumulative volume is 50% of the total volume of the particles. In addition, when measuring with this particle size distribution measuring device, the measurement range is 0.1 to 4.
Set to 5μ. As a result, the calculation is performed using the relationship between the scattered light intensity and the particle diameter derived from the Mie scattering theory formula (built into the measuring device). Further, a standard refractive index of 1.7-0.2i is selected as the refractive index, and a direct calculation method using the least squares theory is used as the calculation method for determining the particle size distribution. The number of measurements for one sample is specified as 7, and the measurement interval is 2 seconds.
【0011】0.1重量%に純水で均一に希釈された試
料は、フローセルを利用して測定されるが、内蔵された
超音波発信器は常時オンとし、少なくとも1分以上は超
音波をあてて凝集を防止した後に測定を行う。本発明に
おける積算体積50%の粒径および3μm以下の粒子の
積算体積割合は、各々平均となる粒径および粒子の分布
を示した値であるが、当該粒径が6μmを超えた場合ま
たは当該積算体積割合が25%未満となると、微粒化セ
ルロースの滑らかなクリーム感がなくなり、喫食時にザ
ラツキ感が発生し、さらに保水性、懸濁分散安定性も低
下してくる。A sample uniformly diluted to 0.1% by weight with pure water is measured using a flow cell, but the built-in ultrasonic transmitter is always on and the ultrasonic wave is applied for at least 1 minute. Measurement is performed after applying the sample to prevent agglomeration. In the present invention, the particle size of 50% of the cumulative volume and the cumulative volume ratio of particles of 3 μm or less are values that indicate the average particle size and particle distribution, respectively, but if the particle size exceeds 6 μm or If the cumulative volume ratio is less than 25%, the smooth creamy feel of the micronized cellulose will disappear, a rough feeling will occur when eaten, and water retention and suspension/dispersion stability will also decrease.
【0012】また、当該粒径が0.3μm未満となるよ
うな微粒化セルロースは、分散時に再凝集を起こすよう
になり、また、製造に長時間を要し、不経済であるとい
う理由で好ましくない。当該微粒化セルロースの水懸濁
液は、水と親和性の高い固体即ち、セルロースの粒子コ
ロイドとして高度な安定性と構造粘性を有する。また、
従来一般に用いられている微結晶セルロースと分散剤、
崩壊剤の複合体に比べてウェット状のセルロースのみで
あり、極めて微粒子化されているためにザラツキや食品
の味に影響を与えることなく、また食品の製造に当たっ
て容易に分散するという特徴を有する。[0012] Furthermore, micronized cellulose having a particle size of less than 0.3 μm is not preferred because it tends to reagglomerate during dispersion, requires a long time to produce, and is uneconomical. do not have. The aqueous suspension of micronized cellulose has high stability and structural viscosity as a solid with high affinity for water, that is, a colloid of cellulose particles. Also,
Conventionally commonly used microcrystalline cellulose and dispersants,
Compared to a disintegrating agent complex, it is only wet cellulose, and because it is extremely finely divided, it does not have a grainy texture or affect the taste of the food, and it is easily dispersed during food production.
【0013】本発明において好適な食品は、嗜好飲料、
乳性飲料、デザート類、調理食品等、加熱工程を必要と
するものであり、具体的には、例えば、カレー、シチュ
ー、ソース、スープ等のレトルト食品、ゼリー、プリン
、アイスクリーム、ヨーグルト等のデザート類、ココア
、ジュース、緑茶、甘酒、汁粉等の嗜好飲料、乳酸菌飲
料、豆乳等の乳性飲料、ホイップクリーム、フラワーペ
ースト等である。これらの食品は、当該食品の製造、保
存、消費の過程で、製造時の加熱殺菌処理、ホットベン
ダーによる消費者への提供、調理等における加熱処理が
施される。この場合、加熱時の熱運動、温度上昇によっ
て、見掛粘度が急激に低下することにより乳化、懸濁状
態の破壊が起こり易い。また、食品自体の収縮、形崩れ
、溶解による組織の変化や破壊が起こり易く離水を伴う
ことがあり、商品価値の低下が問題となっていた。[0013] Suitable foods in the present invention include recreational drinks,
Dairy drinks, desserts, cooked foods, etc. that require a heating process, specifically, retort food such as curry, stew, sauce, soup, jelly, pudding, ice cream, yogurt, etc. Desserts, cocoa, juice, green tea, amazake, sweet drinks such as shiruko, lactic acid bacteria drinks, milk drinks such as soy milk, whipped cream, flower paste, etc. These foods are subjected to heat sterilization treatment during production, provision to consumers by hot vendors, heat treatment during cooking, etc. during the process of manufacturing, preserving, and consuming the foods. In this case, the apparent viscosity rapidly decreases due to thermal movement and temperature rise during heating, which tends to cause emulsification and destruction of the suspended state. In addition, the food itself tends to shrink, lose its shape, and undergo tissue change or destruction due to dissolution, which may result in syneresis, resulting in a reduction in commercial value.
【0014】ところがこのような食品に、上述の微粒化
セルロースを添加することによって加熱に対して乳化、
懸濁、組織の安定な食品組成物の提供が可能となる。微
粒化セルロースを添加しない場合、例えばココア飲料の
製造において加熱殺菌処理によりココアの沈降が起こり
、また、乳化が壊れて油滴が分離し、それが浮上して、
いわゆるオイルリングを容器内壁面に形成するという問
題が生じる。豆乳飲料においては、加熱処理において大
豆タンパク質が凝集し易く、経時的に沈澱を生じる。ま
た、ゼリー、プリン、ヨーグルト等のデザート類の製造
においては、加熱工程を経た製品の保存や、ベーカリー
製品のトッピングに用いる場合、糖液のにじみ出しや、
離水、食品自体の収縮、形崩れ、溶解といった問題が生
じる。However, by adding the above-mentioned micronized cellulose to such foods, the emulsification and
It becomes possible to provide a food composition with stable suspension and structure. If micronized cellulose is not added, for example, in the production of cocoa drinks, cocoa will settle due to heat sterilization, and the emulsification will break and oil droplets will separate and float to the surface.
A problem arises in that a so-called oil ring is formed on the inner wall surface of the container. In soy milk beverages, soy protein tends to aggregate during heat treatment, causing precipitation over time. In addition, in the production of desserts such as jelly, pudding, and yogurt, when preserving the product after the heating process or using it as a topping for bakery products, oozing of the sugar solution,
Problems such as syneresis, shrinkage of the food itself, loss of shape, and dissolution occur.
【0015】これらの食品に、微粒化セルロースを添加
することによって、例えば飲料の場合、微粒子化し、均
一分散したセルロースコロイド粒子のマトリックスに懸
濁粒子を保持すること、乳化状態では油・水界面に吸着
した微粒化セルロースが保護膜を形成すると共に、連続
相に均一分散していること、さらに加熱によって粘度の
低下が起こらないこと等によって、乳化・懸濁の安定化
が可能となる。また、デザート類の場合、微粒子化した
水不溶性のセルロースコロイドであるために、保水性、
耐熱性が著しく向上し、離水や形態変化を起こさず、安
定でザラツキのない滑らかな組織が得られる。[0015] By adding micronized cellulose to these foods, for example, in the case of beverages, it is possible to maintain suspended particles in a matrix of micronized and uniformly dispersed cellulose colloid particles, and in an emulsified state, to maintain the suspended particles at the oil/water interface. Stabilization of emulsification and suspension is possible because the adsorbed micronized cellulose forms a protective film and is uniformly dispersed in the continuous phase, and the viscosity does not decrease due to heating. In addition, in the case of desserts, water-retentive and
Heat resistance is significantly improved, and a stable, smooth structure without roughness is obtained without causing syneresis or morphological changes.
【0016】食品への添加量は、セルロース固形分とし
て0.01〜3.0%が必要である。もちろん、対象と
する食品によって最適な添加量は異なる。0.01%以
下では本発明の目的とする熱に安定な食品組成物が得ら
れず、3.0%以上の添加では粘度の上昇等により本発
明の対象とする食品本来の食感を損ねるという問題が生
じる。[0016] The amount added to food is required to be 0.01 to 3.0% in terms of cellulose solid content. Of course, the optimal amount of addition differs depending on the target food. If it is less than 0.01%, the heat-stable food composition that is the object of the present invention cannot be obtained, and if it is added more than 3.0%, the original texture of the food that is the object of the present invention is impaired due to an increase in viscosity, etc. A problem arises.
【0017】本発明の食品組成物は、微粒化セルロース
と、食品に多用される安定剤を併用することも可能であ
る。一般に食品用安定剤は、保護コロイド性、粘性上昇
による分散粒子の懸濁安定性の付与、吸水性によるボデ
ィの付与、離水防止、テクスチャーの向上、さらに乳化
安定性、耐酸耐塩安定性、泡安定性の付与を目的として
食品により適宜選択して用いられる。この場合、安定剤
のみの使用では糊状感や安定剤特有の味の発現、加熱に
よる温度上昇により急激に粘度が低下し、乳化、懸濁状
態や組織の破壊といった問題が起こるが、微粒化セルロ
ースと併用することにより、これらの問題点を軽減ない
し防止すると共に、好ましい相乗作用を発揮する。[0017] The food composition of the present invention can also contain a combination of micronized cellulose and a stabilizer that is often used in foods. In general, food stabilizers have protective colloidal properties, impart suspension stability to dispersed particles by increasing viscosity, provide body by water absorption, prevent syneresis, and improve texture, as well as emulsion stability, acid and salt resistance stability, and foam stability. It is used by selecting it as appropriate depending on the food for the purpose of imparting sex. In this case, if only a stabilizer is used, problems such as a pasty feeling and taste peculiar to the stabilizer will occur, and the viscosity will rapidly decrease due to temperature rise due to heating, resulting in emulsification, suspension, and destruction of the structure. When used in combination with cellulose, these problems can be alleviated or prevented, and a favorable synergistic effect can be exerted.
【0018】併用できる食品用安定剤としては、例えば
、寒天、カラギーナン、ファーセレラン、アルギン酸類
、ローカストビーンガム、グアーガム、タマリンドガム
、カラヤガム、アラビアガム、ペクチン、キサンタンガ
ム、プルラン、ジェランガム、大豆タンパク質、ゼラチ
ン、レシチン、セルロース誘導体、ポリビニルアルコー
ル、ポリアクリル酸等があげられる。Food stabilizers that can be used in combination include, for example, agar, carrageenan, farcellan, alginic acids, locust bean gum, guar gum, tamarind gum, karaya gum, acacia, pectin, xanthan gum, pullulan, gellan gum, soybean protein, gelatin, Examples include lecithin, cellulose derivatives, polyvinyl alcohol, and polyacrylic acid.
【0019】[0019]
【実施例】次に、参考例、実施例によって本発明をさら
に詳細に説明する。[Examples] Next, the present invention will be explained in more detail by reference examples and examples.
【0020】[0020]
【参考例】市販DPパルプを細断後、10%塩酸中で1
05℃20分間加水分解して得られた酸不溶性残さを濾
過、洗浄した後、固形分10%のセルロース分散液を調
整した。このセルロース分散液を媒体攪拌湿式粉砕装置
(アシザワ株式会社製パールミル、PM5RL型)で、
媒体として直径2mmφのジルコニアビーズを用いて、
攪拌翼回転数1500rpm、セルロース分散液の供給
量0.4l/minの条件で、繰り返し通過によって粉
砕処理を行い三種類の微粒化セルロースを得た。以下、
これらを試料A、B、Cという。得られた微粒化セルロ
ースの積算体積50%の粒径、3μm以下の粒子の積算
体積割合、および固形分を3%に調整した水分散液の2
0℃、80℃における粘度とその比を表1に示す。[Reference example] After shredding commercially available DP pulp,
After filtration and washing of the acid-insoluble residue obtained by hydrolysis at 05° C. for 20 minutes, a cellulose dispersion having a solid content of 10% was prepared. This cellulose dispersion was processed using a media agitation wet grinding device (Pearl Mill, PM5RL model, manufactured by Ashizawa Co., Ltd.).
Using zirconia beads with a diameter of 2 mmφ as a medium,
Three types of atomized cellulose were obtained by repeated pulverization under the conditions of a stirring blade rotation speed of 1500 rpm and a cellulose dispersion supply rate of 0.4 l/min. below,
These are called samples A, B, and C. The particle size of the obtained micronized cellulose at a cumulative volume of 50%, the cumulative volume ratio of particles of 3 μm or less, and the solid content of the aqueous dispersion adjusted to 3%.
Table 1 shows the viscosities at 0°C and 80°C and their ratios.
【0021】[0021]
【実施例1】参考例で得た固形分10%の微粒化セルロ
ース(試料A、B、C)を用い、下記成分のココア飲料
を作成した。
成分
重量(%)ココア末
0.5砂糖
5.0全脂粉乳
0.8食塩
0.05乳化剤
0.2微粒化セルロース
4.0水
残量70℃の温水中に、配
合成分の全量を加え分散させた。
これをマントンゴーリン型ホモジナイザーを用いて15
0kg/cm2 、200kg/cm2 で2段階均質
化処理後、耐熱瓶に充填し、121℃で30分間加熱殺
菌処理を行った。Example 1 Using the micronized cellulose with a solid content of 10% (Samples A, B, and C) obtained in Reference Example, a cocoa drink having the following ingredients was prepared. component
Weight (%) cocoa powder
0.5 sugar
5.0 whole milk powder
0.8 salt
0.05 emulsifier
0.2 Micronized cellulose
4.0 water
The entire amount of the ingredients was added and dispersed in the remaining hot water at 70°C. This was mixed for 15 minutes using a Manton-Gorlin homogenizer.
After two-step homogenization treatment at 0 kg/cm2 and 200 kg/cm2, the mixture was filled into a heat-resistant bottle and heat sterilized at 121°C for 30 minutes.
【0022】次に、100mlの沈降管に移し、25℃
で24時間放置した後のココアの沈積および24時間放
置後のサンプルを手で上下3回、一定速度で振盪再分散
したのち、15分間室温に放置してココアの沈積を観察
した。得られた結果を表2に示す。Next, transfer to a 100ml sedimentation tube and heat at 25°C.
Cocoa deposition after being left for 24 hours and samples after being left for 24 hours were redispersed by hand shaking up and down three times at a constant speed, and then left at room temperature for 15 minutes to observe cocoa deposition. The results obtained are shown in Table 2.
【0023】[0023]
【比較例1】セルロース分散液の供給量、0.7l/m
inで1回通過によることの他は、参考例の方法で、積
算体積50%の粒径が8.80μm、3μm以下の粒子
の積算体積割合5.5%の微粒化セルロース(以下、試
料Dという)を得た。試料Dを用いて実施例1と同様な
方法でココア飲料を作成し、ココアの沈積を観察した。
得られた結果を表2に示す。[Comparative Example 1] Supply amount of cellulose dispersion, 0.7 l/m
Micronized cellulose (hereinafter referred to as sample D) with a particle size of 8.80 μm at 50% of the cumulative volume and 5.5% of the cumulative volume ratio of particles of 3 μm or less was prepared using the method of the reference example, except that it was passed once in ) was obtained. A cocoa drink was prepared using Sample D in the same manner as in Example 1, and the deposition of cocoa was observed. The results obtained are shown in Table 2.
【0024】[0024]
【実施例2】参考例で得た固形分10%の微粒化セルロ
ース(試料B)を用いて、下記成分のスープを作成した
。
成分
重量(%)コーン
13.0α化澱粉
1.0植物油脂
5.
0牛乳
2.0脱脂粉乳
2.0粉あめ
2.0調味料
2.0ホワイトルー
2.0微粒化セルロース
8.0水
残量微粒化セルロー
スを水に分散させた後、加熱攪拌しながら処方成分を溶
解させた。これをマントンゴーリン型ホモジナイザーを
用いて、100kg/cm2 ,250kg/cm2
で2段階均質化処理後、耐熱瓶に充填し、121℃で3
0分間加熱殺菌処理を行い、5℃まで急冷した。[Example 2] Using the micronized cellulose (sample B) with a solid content of 10% obtained in the reference example, a soup with the following ingredients was prepared. component
Weight (%) cone
13.0 Pregelatinized starch
1.0 vegetable oil
5.
0 milk
2.0 skimmed milk powder
2.0 powdered candy
2.0 seasoning
2.0 white roux
2.0 micronized cellulose
8.0 water
After dispersing the remaining amount of micronized cellulose in water, the prescription components were dissolved while stirring with heating. Using a Manton-Gorlin type homogenizer,
After 2-step homogenization treatment, fill in a heat-resistant bottle and incubate at 121℃ for 3
Heat sterilization treatment was performed for 0 minutes and then rapidly cooled to 5°C.
【0025】スープの乳化安定性については、スープ3
00gを500ml容の耐熱瓶に入れ、再度加熱処理(
121℃×30分)した。その後24時間室温下に放置
し、油の分離程度を観察した。スープの懸濁安定性につ
いては、スープ100gを100ml容の沈降管にいれ
、24時間室温下に放置した後、油以外の層分離につい
て観察した。得られた結果を表3に示す。Regarding the emulsion stability of soup, Soup 3
00g into a 500ml heat-resistant bottle and heat-treated again (
(121°C x 30 minutes). Thereafter, the mixture was left at room temperature for 24 hours, and the degree of oil separation was observed. Regarding the suspension stability of the soup, 100 g of the soup was placed in a 100 ml sedimentation tube, and after being left at room temperature for 24 hours, separation of layers other than oil was observed. The results obtained are shown in Table 3.
【0026】[0026]
【比較例2】比較例1で用いた微粒化セルロース(試料
D)を用いて、実施例2と同様な方法でスープを作成し
た。得られた結果を表3に示す。[Comparative Example 2] Using the micronized cellulose (Sample D) used in Comparative Example 1, a soup was prepared in the same manner as in Example 2. The results obtained are shown in Table 3.
【0027】[0027]
【表1】[Table 1]
【0028】[0028]
【表2】[Table 2]
【0029】[0029]
【表3】[Table 3]
【0030】[0030]
【発明の効果】本発明の食品組成物は、加熱による温度
上昇により、粘度の低下が起こらないか、または、上昇
するという特徴を有する微粒化セルロースを安定剤とし
て含む。このため、加熱工程を必要とする食品の製造に
当たって、加熱による乳化、懸濁および組織の破壊を防
止し、長期に安定な食品の製造が可能となる。EFFECTS OF THE INVENTION The food composition of the present invention contains micronized cellulose as a stabilizer, which is characterized in that the viscosity does not decrease or increases when the temperature increases due to heating. Therefore, when producing foods that require a heating process, it is possible to prevent emulsification, suspension, and tissue destruction due to heating, and to produce foods that are stable over a long period of time.
【0031】また、本発明の食品組成物は食品用安定剤
を併用することによりさらに安定性が向上する。この場
合、食品用安定剤のみによる安定性付与に比べて、糊状
感や極端な粘度上昇が低減され、さっぱりした食感を与
える。さらに、本発明の食品組成物に添加する微粒化セ
ルロースは、極めて微粒化されているために、ザラツキ
や食品の味に影響を与えることがなく、また、ウェット
状であるために分散し易く食品の製造が容易に行い得る
。Furthermore, the stability of the food composition of the present invention can be further improved by using a food stabilizer in combination. In this case, compared to stabilization using only a food stabilizer, the pastiness and extreme increase in viscosity are reduced, giving a refreshing texture. Furthermore, since the micronized cellulose added to the food composition of the present invention is extremely micronized, it does not affect the graininess or taste of the food, and since it is in a wet form, it is easily dispersed in the food. can be easily manufactured.
Claims (1)
m、3μm以下の粒子の積算体積割合が25%以上、温
度上昇による見掛粘度の比が1以上の微粒化セルロース
を固形分で0.01〜3.0%添加することを特徴とす
る加熱に対して乳化、懸濁、組織の安定な食品組成物。[Claim 1] Particle size of 50% of cumulative volume is 0.3 to 6μ
Heating characterized by adding 0.01 to 3.0% solid content of micronized cellulose in which the cumulative volume ratio of particles of m, 3 μm or less is 25% or more, and the ratio of apparent viscosity due to temperature rise is 1 or more. Stable food compositions for emulsification, suspension, and organization.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3097219A JP2981299B2 (en) | 1991-04-26 | 1991-04-26 | Heat stable food composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3097219A JP2981299B2 (en) | 1991-04-26 | 1991-04-26 | Heat stable food composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04325060A true JPH04325060A (en) | 1992-11-13 |
| JP2981299B2 JP2981299B2 (en) | 1999-11-22 |
Family
ID=14186523
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3097219A Expired - Fee Related JP2981299B2 (en) | 1991-04-26 | 1991-04-26 | Heat stable food composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2981299B2 (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH11178517A (en) * | 1997-12-25 | 1999-07-06 | Sanei Gen Ffi Inc | Dispersion stabilized composition |
| JP2000511061A (en) * | 1996-05-28 | 2000-08-29 | エフ エム シー コーポレーション | Cellulose composition, its manufacture and its use in food |
| JP2004242670A (en) * | 2003-01-20 | 2004-09-02 | Mitsubishi Chemicals Corp | Emulsion stabilizer and milk drink containing the same |
| JP2004248536A (en) * | 2003-02-18 | 2004-09-09 | Asahi Kasei Chemicals Corp | Heat resistant gel |
| JP2004305005A (en) * | 2003-04-01 | 2004-11-04 | Asahi Kasei Chemicals Corp | Method for stabilizing dairy-containing beverage |
| JP2006025743A (en) * | 2004-07-20 | 2006-02-02 | Mitsubishi Chemicals Corp | Emulsification stabilizer and milk beverage containing the same |
| JP2009189369A (en) * | 2009-04-27 | 2009-08-27 | Mitsubishi Chemicals Corp | Emulsion stabilizer for milk beverage and milk beverage containing the same |
| JP2020068712A (en) * | 2018-10-31 | 2020-05-07 | 三栄源エフ・エフ・アイ株式会社 | Emulsion composition having milk flavor, method for producing the same and method for improving flavor of emulsion composition having milk flavor |
-
1991
- 1991-04-26 JP JP3097219A patent/JP2981299B2/en not_active Expired - Fee Related
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2000511061A (en) * | 1996-05-28 | 2000-08-29 | エフ エム シー コーポレーション | Cellulose composition, its manufacture and its use in food |
| JPH11178517A (en) * | 1997-12-25 | 1999-07-06 | Sanei Gen Ffi Inc | Dispersion stabilized composition |
| JP2004242670A (en) * | 2003-01-20 | 2004-09-02 | Mitsubishi Chemicals Corp | Emulsion stabilizer and milk drink containing the same |
| JP2004248536A (en) * | 2003-02-18 | 2004-09-09 | Asahi Kasei Chemicals Corp | Heat resistant gel |
| JP2004305005A (en) * | 2003-04-01 | 2004-11-04 | Asahi Kasei Chemicals Corp | Method for stabilizing dairy-containing beverage |
| JP2006025743A (en) * | 2004-07-20 | 2006-02-02 | Mitsubishi Chemicals Corp | Emulsification stabilizer and milk beverage containing the same |
| JP2009189369A (en) * | 2009-04-27 | 2009-08-27 | Mitsubishi Chemicals Corp | Emulsion stabilizer for milk beverage and milk beverage containing the same |
| JP2020068712A (en) * | 2018-10-31 | 2020-05-07 | 三栄源エフ・エフ・アイ株式会社 | Emulsion composition having milk flavor, method for producing the same and method for improving flavor of emulsion composition having milk flavor |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2981299B2 (en) | 1999-11-22 |
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