JPS58304B2 - Simultaneous purification of lactose and casein - Google Patents
Simultaneous purification of lactose and caseinInfo
- Publication number
- JPS58304B2 JPS58304B2 JP119878A JP119878A JPS58304B2 JP S58304 B2 JPS58304 B2 JP S58304B2 JP 119878 A JP119878 A JP 119878A JP 119878 A JP119878 A JP 119878A JP S58304 B2 JPS58304 B2 JP S58304B2
- Authority
- JP
- Japan
- Prior art keywords
- lactose
- casein
- solution
- activated carbon
- crude
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 title claims description 44
- 239000008101 lactose Substances 0.000 title claims description 44
- 239000005018 casein Substances 0.000 title claims description 30
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 title claims description 30
- 235000021240 caseins Nutrition 0.000 title claims description 30
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 title claims description 20
- 238000000746 purification Methods 0.000 title claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 43
- 239000007788 liquid Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 8
- 239000000243 solution Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 8
- 241000894006 Bacteria Species 0.000 description 7
- 230000008929 regeneration Effects 0.000 description 7
- 238000011069 regeneration method Methods 0.000 description 7
- 239000011259 mixed solution Substances 0.000 description 6
- 238000001179 sorption measurement Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000001580 bacterial effect Effects 0.000 description 3
- 235000018102 proteins Nutrition 0.000 description 3
- 102000004169 proteins and genes Human genes 0.000 description 3
- 108090000623 proteins and genes Proteins 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 239000001842 Brominated vegetable oil Substances 0.000 description 1
- 239000005862 Whey Substances 0.000 description 1
- 102000007544 Whey Proteins Human genes 0.000 description 1
- 108010046377 Whey Proteins Proteins 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004332 deodorization Methods 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000000909 electrodialysis Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004519 manufacturing process Methods 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
- 238000002156 mixing Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Description
【発明の詳細な説明】
本発明は乳糖とカゼインを同じ溶液中で効率よく精製す
る方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for efficiently purifying lactose and casein in the same solution.
更に詳細には、本発明は、メイラード反応を防止し、か
つ通液中断時における腐敗を防止しつつ乳糖とカゼイン
を同時に精製する方法に関するものである。More specifically, the present invention relates to a method for simultaneously purifying lactose and casein while preventing the Maillard reaction and preventing spoilage when fluid flow is interrupted.
一般に、乳糖及びカゼインはそもそも同じ牛乳中にあっ
て、使用するときも多くの食品において同時に用いられ
ている。Generally, lactose and casein are found in the same milk and are used together in many foods.
しかしながら、乳糖とカゼインは別々に分離され、精製
されて各別の製品となり、市販されている状態である。However, lactose and casein are separately separated and purified into separate products that are commercially available.
このように各別に製品化された乳糖とカゼインはユーザ
ーの手に渡って、ここで混合されて各食品の製造に使用
されることになる。The lactose and casein produced separately in this way are delivered to users, where they are mixed and used in the production of various foods.
従って、乳糖とカゼインが一定の割合で混合されていて
も何ら支障はなく、ユーザーにとってはむしろ好都合と
いえることである。Therefore, there is no problem even if lactose and casein are mixed at a certain ratio, and it can be said that it is rather convenient for the user.
一方、乳糖とカゼインはそのほとんどが輸入されている
が、それらは未だ精製されておらず、風味は悪く、色調
も悪い場合がある。On the other hand, lactose and casein are mostly imported, but they are not yet refined and may have a bad flavor and color.
そこで、乳糖とカゼインの精製が行なわれることになる
が、従来は、乳糖とカゼインを別々にそれぞれ異なった
条件で精製するのが普通であった。Therefore, lactose and casein are purified, but conventionally it has been common to purify lactose and casein separately under different conditions.
例えば、カゼインの精製法としては、特公昭45−19
616号公報に示される如く、カゼインをアルカリ溶液
で溶解し、pH6,0〜7.5で、40℃以下で粒状活
性炭処理する方法が知られ、また、乳糖の精製法として
は、特開昭52−117445号公報に示される如く、
ホエーを70℃以下で活性炭処理し、次いでイオン交換
電気透析装置で処理する方法が知られている。For example, as a method for purifying casein,
As shown in Japanese Patent Publication No. 616, a method is known in which casein is dissolved in an alkaline solution and treated with granular activated carbon at pH 6.0 to 7.5 and below 40°C. As shown in Publication No. 52-117445,
A method is known in which whey is treated with activated carbon at 70° C. or lower and then treated with an ion exchange electrodialysis device.
乳糖とカゼインはいずれは混合されて用いられる場合が
多いために、精製に先だって混合し、同時に精製しより
とすることも試みられるが、両者の混合状態にあるとき
は、糖と蛋白の反応であるメイラード反応がきわめて起
りやすく、褐変化が生じ、また、糖羨蛋白が同時に存在
するために細菌の増殖が盛んとなり、きわめて腐敗しや
すくなってしまい、とうてい乳糖とカゼインを同時に精
製することが実施化されることはなかった。Since lactose and casein are often used as a mixture, attempts have been made to mix them before purification and purify them at the same time, but when the two are in a mixed state, the reaction between sugar and protein occurs. A certain Maillard reaction is extremely likely to occur, resulting in browning, and the simultaneous presence of glycoenzyme proteins promotes bacterial growth, making it extremely susceptible to spoilage. It was never made public.
しかし、本発明者らは、乳糖とカゼインの同時精製が、
カラム増設等の設備投資の半減(カラム1塔式により2
塔式の活性炭量と同じにすれば吸着帯の長さが1/2近
くになり、通液時間が延長され再生頻度の減少による労
務費及び再生費用の低減活ヰ炭取換え時間の延長等)ラ
ンニングコストの低減など大きな経費の節約につながる
ところから、同時精製の研究を行った。However, the present inventors found that simultaneous purification of lactose and casein
Capital investment for column expansion etc. is halved (2 columns due to 1 column type)
If the amount of activated carbon is the same as that of the tower type, the length of the adsorption zone will be nearly halved, extending the liquid passage time and reducing the regeneration frequency, reducing labor costs and regeneration costs.Extending the time for replacing activated carbon, etc. ) We conducted research on simultaneous refining as it would lead to significant cost savings such as reduced running costs.
そして、ここに、本発明において乳糖とカゼインの混合
溶液を45〜65℃、好ましくは50〜60℃の温度を
維持しつつ1種もしくは2種以上の粒状活性炭で処理す
ることによって通液前後においてメイラード反応を起す
ことなく同時精製を可能としたのである。Here, in the present invention, a mixed solution of lactose and casein is treated with one or more types of granular activated carbon while maintaining a temperature of 45 to 65 °C, preferably 50 to 60 °C, before and after passing the solution. This enabled simultaneous purification without causing the Maillard reaction.
また、本発明では適宜混合溶液の通液を中断し、その間
に30%濃度以上の乳糖溶液、好ましくは45〜65℃
の範囲の乳糖溶液を循環通液することによって細菌の増
殖を抑え、腐敗を完全に防止することに成功したのであ
る。In addition, in the present invention, the flow of the mixed solution is interrupted as appropriate, and during that time, the lactose solution with a concentration of 30% or more is added, preferably at 45 to 65 °C.
By circulating a lactose solution in the following range, they succeeded in suppressing bacterial growth and completely preventing spoilage.
この方法で腐敗が防止されるので、活性炭の再生頻度を
減少きせることができる。In this way, spoilage is prevented and the frequency of activated carbon regeneration can be reduced.
本発明においては、まず、市販の粗製乳糖が70〜80
℃の水に溶解される。In the present invention, first, commercially available crude lactose is 70 to 80%
Dissolved in water at ℃.
粗製乳糖の濃度としては20〜50%程度にすることが
望ましい。The concentration of crude lactose is preferably about 20 to 50%.
この溶液は45〜65℃に冷却されるが、不溶性たんば
く質が多い場合、活性炭層に目詰りが生じることから、
フィルタープレス、フンダフィルター等でろ過助剤を加
えて除たんばくするのが好ましい。This solution is cooled to 45-65°C, but if there is a large amount of insoluble protein, the activated carbon layer will become clogged.
It is preferable to remove dust by adding a filter aid using a filter press, funda filter, etc.
一方、市販の粗製アルカリカゼインを炭酸ナトリウムや
炭酸カリウム等のアルカリ剤で80℃に溶解させた後、
45〜65℃に冷却する。On the other hand, after dissolving commercially available crude alkaline casein with an alkaline agent such as sodium carbonate or potassium carbonate at 80°C,
Cool to 45-65°C.
粗製アルカリカゼインの濃度は適宜でよいが、5〜13
楚程度が適当である。The concentration of crude alkaline casein may be set as appropriate, but it is between 5 and 13.
Chu level is appropriate.
ここに得られた粗製乳糖溶液と粗製カゼイン溶液は、目
的により適当な割合で混合され、その液温を45〜65
℃、好ましくは50〜60℃に調整される。The crude lactose solution and crude casein solution obtained here are mixed in an appropriate ratio depending on the purpose, and the liquid temperature is adjusted to 45 to 65.
℃, preferably adjusted to 50 to 60℃.
液温か45℃より低温のときは乳糖の結晶がでやすく、
その結果口づまりを起すことがあって好ましくなく、ま
た65℃より高温のときは乳糖とカゼインでメイラード
反応を起しやすくなって、活性炭の吸着能力の低下及び
精製液において着色を生じることがあって好ましくない
。When the temperature of the liquid is lower than 45℃, lactose crystals are likely to form.
As a result, it may cause clogging, which is undesirable.Also, when the temperature is higher than 65°C, the Maillard reaction between lactose and casein tends to occur, which may reduce the adsorption capacity of activated carbon and cause coloration in the purified liquid. Undesirable.
液温45〜65℃の混合溶液は1種もしくは2種以上の
粒状活性炭に通液される。The mixed solution having a liquid temperature of 45 to 65°C is passed through one or more types of granular activated carbon.
粒状活性炭は1種類でもよいが、好ましいのは2種類、
即ち、脱臭用粒状活性炭と脱色用粒状活性炭を併用する
ことである。One type of granular activated carbon may be used, but two types are preferable.
That is, the granular activated carbon for deodorization and the granular activated carbon for decolorization are used together.
併用する際は、両者混合して同−塔に入れてもよく、別
々の塔に別々に各活性炭を入れてもよい。When used in combination, both may be mixed and placed in the same column, or each activated carbon may be placed separately in separate columns.
液温45〜65℃の混合溶液は粒状活性炭を固定した塔
に通液させるが、通液及び循環中液温が45〜65℃の
範囲をはずれないように管理し、必要があれば加温装置
をつけて45℃、好ましくは50℃を下らないようにし
なければならない。The mixed solution with a liquid temperature of 45 to 65°C is passed through a column fixed with granular activated carbon, but the liquid temperature is controlled so that it does not fall outside the range of 45 to 65°C during the passage and circulation, and if necessary, it is heated. The temperature of the apparatus must not fall below 45°C, preferably 50°C.
液温45℃以下になると乳糖が結晶化したり、細菌が増
殖して腐敗するので45℃以上で実施せねばならない。If the liquid temperature is below 45°C, lactose will crystallize and bacteria will proliferate and putrefy, so it must be carried out at a temperature above 45°C.
本発明においては、液温45〜65℃の混合溶液を粒状
活性炭の破過点(活性炭の吸着能力が減少する点)まで
連続精製することが可能であるが。In the present invention, it is possible to continuously purify a mixed solution having a liquid temperature of 45 to 65° C. up to the breakthrough point of granular activated carbon (the point at which the adsorption capacity of activated carbon decreases).
破過点はきわめて長く、普通、破過点までの間にしばし
ば休止することがある。The breakthrough point is very long and there are usually many pauses between the breakthrough points.
一旦液温45〜65℃での通液を休止すると、たちまち
細菌が増殖して腐敗し再生処理が必要となってしまう。Once the flow of liquid at a temperature of 45 to 65° C. is stopped, bacteria will immediately proliferate and putrefy, necessitating regeneration treatment.
本発明においては、通液を休止したときは直ちに30%
以上、好ましくは30〜50%で、45〜65℃の乳糖
水溶液を循環すせることによって、再生処理をすること
なく破過点までの連続再使用を可能とする。In the present invention, when fluid flow is stopped, 30%
By circulating an aqueous lactose solution of preferably 30 to 50% and at 45 to 65°C, continuous reuse up to the breakthrough point is possible without regeneration treatment.
30%以上の乳糖水溶液は細菌の増殖を抑えることがで
き、しかもその後に乳糖とカゼインの混合液が直接通液
されても同じ乳糖であるために製品中へ何らの障害もも
たらすことはない。A 30% or more lactose aqueous solution can suppress the growth of bacteria, and even if a mixture of lactose and casein is directly passed through the product afterwards, it will not cause any problems in the product since it is the same lactose.
従って1通液中断時に普通性なわれている長時間の水洗
も全く必要としない。Therefore, there is no need for a long period of washing with water, which is common when one liquid flow is interrupted.
次に本発明の試験例及び実施例を示す。Next, test examples and examples of the present invention will be shown.
試験例 1
精製乳糖40%(W/W)、粗製カゼイン10%(W/
W)の水溶液を重量比3:1で混合せしめた後100m
1づつ3部に分け、それぞれ80℃、60℃、40℃に
調整した恒温槽内で5〜7時間静置し、1時間毎にそれ
ぞれの褐変化状態をみた。Test example 1 Purified lactose 40% (W/W), crude casein 10% (W/W)
100 m after mixing the aqueous solution of W) at a weight ratio of 3:1.
The mixture was divided into 3 portions and allowed to stand for 5 to 7 hours in a constant temperature bath adjusted to 80°C, 60°C, and 40°C, and the state of browning was observed every hour.
着色はTBA値(E443)で測定。Coloring is measured by TBA value (E443).
その結果は第1図に示される通りで、40℃、60℃で
は褐変化されず、80℃では急激に褐変化することを示
す。The results are shown in Figure 1, showing that there is no browning at 40°C or 60°C, but there is a rapid browning at 80°C.
試験例 2
温水ジャケットのついたカラム(200ml容)に粒状
活は炭(アトスターBI−L:二村化学工業製とクラレ
コールGLO:クラレケミカル製、2:1混合物)を充
填して用意した。Test Example 2 A column (200 ml volume) equipped with a hot water jacket was prepared by filling granular activated charcoal (Atostar BI-L: manufactured by Futamura Chemical Industry Co., Ltd. and Kuraray Coal GLO: manufactured by Kuraray Chemical Co., Ltd., a 2:1 mixture).
一方5〜40%の精製乳糖の水溶液を作り、それぞれ3
7℃と50℃に加温して用意した。On the other hand, make an aqueous solution of 5-40% purified lactose, and
They were prepared by heating them to 7°C and 50°C.
上記の溶液を上記装置で空中細菌をとりいれながらLv
2m/Hrで循環させた。While introducing the above solution with the above device and introducing airborne bacteria,
It was circulated at 2 m/Hr.
50℃の各乳糖溶液については10日後に溶液中の細菌
数を検出し、37℃の各乳糖溶液については3日後と6
日後に溶液中の細菌数を検出した。For each lactose solution at 50°C, the number of bacteria in the solution was detected after 10 days, and for each lactose solution at 37°C, after 3 days and 6 days.
After a day, the number of bacteria in the solution was detected.
その結果は第2図に示されるが、37℃のものは細菌が
増殖しているのに対し、50℃のものは全く増殖してい
ないのが分る。The results are shown in Figure 2, and it can be seen that bacteria are growing at 37°C, but not at all at 50°C.
実施例
粗製乳糖100Kgを50℃の温水150Kgに加え、
70〜80℃で攪拌溶解させた後に50℃に冷却する。Example 100 kg of crude lactose was added to 150 kg of 50°C warm water,
After stirring and dissolving at 70 to 80°C, the mixture is cooled to 50°C.
一方、粗製カゼイン10Kgを50℃の温水100Kg
に分散させた後、炭酸カリウム(無水)390gを添加
80℃で攪拌容解後、50℃に冷却する。On the other hand, add 10kg of crude casein to 100kg of warm water at 50°C.
After dispersing the mixture, 390 g of potassium carbonate (anhydrous) was added, stirred and dissolved at 80°C, and then cooled to 50°C.
両者を全量混合し、50℃の温度に保持しつつ、活性炭
充填層高150cm、通液線速度3m/Hrで粒状活性
炭(アトスターBI−L:二村化学工業、クラレコール
GLC,wet type:クラレケミカルの2:1混
合)カラムを通過させ精製液を得る。Both were mixed in their entire amounts, and while maintaining the temperature at 50°C, granular activated carbon (Atostar BI-L: Futamura Chemical Co., Ltd., Kuraray Coal GLC, wet type: Kuraray Chemical Co., Ltd. 2:1 mixture) to obtain a purified solution.
通液は1回だけで精製された乳糖とカゼインの混合溶液
を得た。A mixed solution of purified lactose and casein was obtained by passing the solution only once.
この溶液は完全に脱色され、脱臭されていた。This solution was completely bleached and deodorized.
4時間の通液作業が完了した後、直ちに40%濃度、6
0℃の乳糖溶液に切り換え、20時間循環通液した。Immediately after completing the 4-hour passage, the concentration was 40%, 6
The solution was switched to a lactose solution at 0° C., and the solution was circulated for 20 hours.
再び、前記粗製乳糖と粗製カゼインの溶液を通液して精
製処理を行った。The solution of the crude lactose and crude casein was passed through the solution again for purification.
次いで、更に40%、60℃の乳糖溶液を20時間循環
通液した。Then, a further 40% lactose solution at 60°C was circulated for 20 hours.
上記くり返し操作を25〜30日間続け、破過へが来た
ので、80℃の2%苛姓ソーダ溶液を通液し、再生処理
した。After repeating the above operation for 25 to 30 days, a breakthrough was reached, and a 2% caustic soda solution at 80° C. was passed therethrough for regeneration treatment.
活性炭再生品は新炭と比較して脱色および脱臭の吸着能
力は85〜80%に減少したが、それ以降再生回数を増
加しても殆んど吸着能力は減少しなかった。The decolorizing and deodorizing adsorption capacity of the recycled activated carbon product decreased to 85 to 80% compared to fresh carbon, but the adsorption capacity hardly decreased even if the number of regenerations was increased thereafter.
第1図は試験例1におけるカゼインと乳糖混合液の褐変
化を試験した図で、第2図は試験例2における乳糖溶液
中の空中細菌増殖度を試験した図である。
A・・・・・・50℃で10日後を示す。
B・・・・・・37℃で3日後を示す。
C・・・・・・37℃で6日後を示す。(4)FIG. 1 is a diagram showing the browning of the casein and lactose mixture in Test Example 1, and FIG. 2 is a diagram showing the degree of aerial bacterial growth in the lactose solution in Test Example 2. A: 10 days after heating at 50°C. B: Shows the results after 3 days at 37°C. C: Shows 6 days at 37°C. (4)
Claims (1)
〜65℃において1種もしくは2種以上の粒状活性炭処
理せしめることを特徴とする乳糖とカゼインの同時精製
法。 2 粗製乳糖溶液と未精製カゼイン溶液を混合し、45
〜65℃において1種もしくは2種以上の粒状活性炭処
理せしめ、適宜通液を中断し、その間は30%(W/W
)濃度以上の乳糖溶液を循環せしめることを特徴とする
乳糖とカゼインの同時精製法。 3 特許請求の範囲第2項における30%(W/W)濃
度以上の乳糖溶液が45〜65℃であることを特徴とす
る乳糖とカゼインの同時精製法。[Claims] 1. Mix a crude lactose solution and an unpurified casein solution,
A method for simultaneous purification of lactose and casein, which comprises treating with one or more types of granular activated carbon at ~65°C. 2 Mix the crude lactose solution and unpurified casein solution,
Treat with one or more types of granular activated carbon at ~65°C, interrupt the flow of liquid as appropriate, and maintain a 30% (W/W)
) A method for simultaneous purification of lactose and casein, characterized by circulating a lactose solution with a concentration higher than that of the lactose solution. 3. A method for simultaneous purification of lactose and casein according to claim 2, characterized in that the lactose solution with a concentration of 30% (W/W) or more is at 45 to 65°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP119878A JPS58304B2 (en) | 1978-01-11 | 1978-01-11 | Simultaneous purification of lactose and casein |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP119878A JPS58304B2 (en) | 1978-01-11 | 1978-01-11 | Simultaneous purification of lactose and casein |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5495745A JPS5495745A (en) | 1979-07-28 |
JPS58304B2 true JPS58304B2 (en) | 1983-01-06 |
Family
ID=11494751
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP119878A Expired JPS58304B2 (en) | 1978-01-11 | 1978-01-11 | Simultaneous purification of lactose and casein |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58304B2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59173099A (en) * | 1983-03-22 | 1984-09-29 | 和光堂株式会社 | Non-crystal type sugar powder |
-
1978
- 1978-01-11 JP JP119878A patent/JPS58304B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5495745A (en) | 1979-07-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS58880B2 (en) | A mixture of granular activated carbon and bone charcoal that has a high ability to remove colored substances from sugar solution | |
JPS58304B2 (en) | Simultaneous purification of lactose and casein | |
US2261919A (en) | Manufacture of sirup | |
EP0001470A1 (en) | A process for enzymatic treatment of waste water of wheat starch plants | |
US2555213A (en) | Method of making lactose | |
US3163538A (en) | Method for increasing the albumen stability of beer | |
US1533033A (en) | Process for treating liquids | |
SU946488A1 (en) | Method of producing protein concentrate of green plant juice | |
US2216753A (en) | Treatment of sugar solutions | |
PL82742B1 (en) | ||
RU2669349C1 (en) | Method for producing lysozyme-containing biologically active additive | |
US3960666A (en) | Preparation of an enzyme-cellulose complex | |
RU2155814C1 (en) | Method of producing sugar from raw sugar cane | |
US2082425A (en) | Process for decolorizing sugar juices | |
SU1397017A1 (en) | Method of obtaining clarified dry blood | |
RU2078826C1 (en) | Method of refining the diffusion or cellular juice of sugar-containing raw | |
SU442800A1 (en) | The method of obtaining the drug for parenteral protein nutrition | |
JPH03195483A (en) | Method for producing vegetable juice | |
US2337853A (en) | Manufacture of dextrose | |
JPS6322786B2 (en) | ||
SU1132950A1 (en) | Method of obtaining clarified dry blood | |
SU709533A1 (en) | Method of preparing ammonium sulfate | |
RU2199874C2 (en) | Method of purifying lactoserum in lactose production | |
JPS60118294A (en) | Treatment of corn-starch waste solution | |
JPS6012014B2 (en) | Production method of enzyme-treated gelatin powder |