JPS58202A - Removing method for solvent in solution and suspension - Google Patents

Removing method for solvent in solution and suspension

Info

Publication number
JPS58202A
JPS58202A JP9861381A JP9861381A JPS58202A JP S58202 A JPS58202 A JP S58202A JP 9861381 A JP9861381 A JP 9861381A JP 9861381 A JP9861381 A JP 9861381A JP S58202 A JPS58202 A JP S58202A
Authority
JP
Japan
Prior art keywords
kneader
kneading
solns
kneaded
water
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
Application number
JP9861381A
Other languages
Japanese (ja)
Other versions
JPH0333361B2 (en
Inventor
Takeo Satake
佐竹 猛雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NIPPON KEMUTETSUKU CONSULTING KK
Nippon Chemtec Consulting Inc
Original Assignee
NIPPON KEMUTETSUKU CONSULTING KK
Nippon Chemtec Consulting Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by NIPPON KEMUTETSUKU CONSULTING KK, Nippon Chemtec Consulting Inc filed Critical NIPPON KEMUTETSUKU CONSULTING KK
Priority to JP9861381A priority Critical patent/JPS58202A/en
Publication of JPS58202A publication Critical patent/JPS58202A/en
Publication of JPH0333361B2 publication Critical patent/JPH0333361B2/ja
Granted legal-status Critical Current

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  • Extraction Or Liquid Replacement (AREA)

Abstract

PURPOSE:To remove solvents from he inside of solns. econimically by adding the solns. into high viscoelastic bodies under kneading beforehand with solvents and kneading these together. CONSTITUTION:High viscoelastic bodies having intrinsically no affinity to solvents are beforehand kneaded under high shearing forces, and solns. are added to these and the kneading is continued, whereby the solvents are removed from the solns. and the degree of concn. is increased. For example, in one embodiment, an aq. 10% gelatin-contg. soln. is kneaded for 30min. at a 40rpm kneader in order to concentrate an aq. gelatin soln., and the concn. of the geletin when this is kneaded at about the flow rate at which the surface under kneading is visible is 16%.

Description

【発明の詳細な説明】 本発明は予め混線中の高粘弾性体中El皺を加え、こo
H筐を高粘弾性体と一鐘に混練することに依り溶液中よ
***を除去することKWRするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention adds El wrinkles to the highly viscoelastic material in the crosstalk in advance, and
The KWR is to remove *** from the solution by kneading the H-casing with a highly viscoelastic material.

溶液中よ少溶媒を***するに社蒸発、蒸製、透析、滲
透等古くから既に用−られて−るが、これらの方法は何
れも熱量の消費が大11f1hつ′に塾、駿備が高価で
あった〉して経済的に常に満足すぺ龜ものとは云い難い
・ 本夷明轄上記の細自難点を含むことなく工業的に有用な
溶媒lI*方法を開発したものである**よ壷溶媒を*
**する方決鯰こ0溶媒と本質的KII和餘をもつ′C
い驚−高粘弾体をあらかじめ高剪断力下虻誕練し、と#
Lに***を添加し轟練會l!妙ることに依勤連處する
ことが出来る。
Evaporation, steaming, dialysis, permeation, etc. have been used for a long time to remove small amounts of solvent in solutions, but all of these methods consume a large amount of heat. However, it is difficult to say that it is always economically satisfactory as it was expensive.The present invention has developed an industrially useful solvent lI* method that does not have the above-mentioned disadvantages. **Give me a pot of solvent*
** If you decide to use a 'C' with zero solvent and essential KII
Surprise - Highly viscoelastic material is trained under high shear force in advance, and #
Add *** to L and have a training session! Strangely enough, I am able to continue working.

ここで云う高粘弾性体と韓タール、アスファルト、アタ
クチックポリブーピレン、ぎリビエルアルコール水II
液、(ラチン水**、m湯水溶液O如自、ある一定温度
で高v&Ili弾性を示す物質を貴う。
The highly viscoelastic materials mentioned here include Korean tar, asphalt, atactic polybupylene, and Gilibiel alcoholic water II.
liquid, (latin water**, m hot water solution O), a substance that exhibits high v&Ili elasticity at a certain temperature.

iuiが親油性の場合親水像高S弾性体、溶媒が親水性
の場合、親油性高粘弾性体が適当である。
When iui is lipophilic, a hydrophilic high S elastic material is suitable, and when the solvent is hydrophilic, a lipophilic high viscoelastic material is suitable.

次に高粘弾性体と社誘発WliO場合高IIWII力を
与える場合曳糸性を示す物質を云う。
Next, in the case of a highly viscoelastic material and a material that exhibits stringiness when a high IIWII force is applied.

本発明#C襲−て高粘弾性体に高剪断力を与える方法は
、高い剪断力を与え、6要に応じJを加熱X線冷却し得
るも0”e&れ社ど011′1に方法、装置でもよい。
The method of applying high shearing force to a highly viscoelastic body using #C of the present invention is to apply a high shearing force and, if necessary, to heat and cool J by X-rays. , or a device.

ニーダ−、パンパV−を今す−、スタリ畠會プレス等O
曽通O滉練−が便利KM%pられる・更らに高粘弾性を
与え為方決K”)いて鯰温度〇−節、第三物質O添加等
ど0@な手段を併用してもよく特定の方法の指定社無い
。要するに高剪断力下で曳糸性を示す方法でよい。
Kneader, Pampa V-now, Stari Hatakekai Press, etc.
It is convenient to use KM%p, which gives even higher viscoelasticity, and even if you use other methods such as catfish temperature, adding a third substance, etc. There is no one company that specifies a specific method.In short, any method that exhibits stringiness under high shear force will suffice.

本発明に於いて溶液を高剪断力下で混練して−る高粘弾
性体中沢加えて混練することに依シ11WktIXW&
*される機構に関しては必ずしも明らかてはないが、混
練している高粘弾性体中に先ずS*がt111込會れ、
そのII混練に依砂これら溶*#11111に小さい粒
子に細分化され、これらに高剪断力が作用し系外に溶媒
が液体状態で放出されるので社な−かと考えられる。
The present invention relies on adding and kneading a highly viscoelastic material Nakazawa to which the solution is kneaded under high shear force.
* Although the mechanism by which this occurs is not necessarily clear, S* is first mixed with t111 in the highly viscoelastic material being kneaded, and
It is thought that this is because during the II kneading, these molten particles are finely divided into small particles, a high shear force is applied to these particles, and the solvent is released from the system in a liquid state.

以下実施例にて誘発wRを具体的に説明する。The induced wR will be specifically explained below in Examples.

実施例1. 水のWk* 予め60/80アスファルト1300grを5tニーダ
−(ii1転数5 Or、p、m ) Kて混線し、系
の温度を50℃に保ち、これに水1000巳を加え、ア
スファルト中沢水を400鑑Wki11させた。この系
は若干茶色昧を帯びた黒色の粘弾性体である。
Example 1. Water Wk * 1300gr of 60/80 asphalt was mixed in a 5t kneader (ii1 rotation number 5 Or, p, m) K in advance, the temperature of the system was kept at 50℃, 1000g of water was added to this, and asphalt Nakazawa water was mixed. I made 400 books Wki11. This system is a slightly brownish black viscoelastic body.

この系にニーダーの内部がみえる様にオープンにしてニ
ーダ−の滉練藺がみえる様に徐々に(200〜300f
fi宛)水を添加し、約2時間に夏や2500鑑の水を
加えた。ニーダ−中O混Il系の温度dジャケラ)Kて
50℃に保った。
This system is opened so that the inside of the kneader can be seen, and gradually (from 200 to 300 f.
Fi) Added water, and added summer and 2500 bottles of water for about 2 hours. The temperature of the O mixed Il system in the kneader was maintained at 50°C.

2時間後ニーダーよりII散じた水の量a660=であ
シ、アスファルト中に含まれてかろ水は500gばあっ
た。従って1740億の水は失われて一九〇 次にニーダ−O上郁璽會軟遺し、上部よ〉出た水が凝纏
し、ニーダ−中に夏るsnc*mコンデンサーを付けた
。同じ実験で失われた水社2500 ff101111
に対し15gr”e&−z&。
After 2 hours, the amount of water dispersed from the kneader was 660 = 500 g. Therefore, 174 billion of water was lost and the kneader O was left in the 190th year, and the water that came out from the top condensed and was installed in the kneader with an SNC*M condenser. Suisha 2500 FF101111 lost in the same experiment
15gr”e&-z&.

実施例2 グリセリン 水**omm 10sO/9−に9ンl會−b**ll (を水)10
00ael予め50℃、上部−放下ostz−グー中で
6 o r、p、tnf謳練中の60/80アス7アル
) 1300 gr 中に加え混線を続けた。
Example 2 Glycerin Water**omm 10sO/9-9-1-b**ll (Water) 10
00ael was added to 1300 gr of 60/80 ascension (60/80 as 7 al) which had been heated in advance at 50° C. in an upper-lowering ostz-goo and continued to mix.

ニーダ−Kg加する甘木aS々に混練している画が上部
よシ確at出来るl1ljlK添加し友。
Kneader - Kg is added to Amagi AS to make sure that the kneading image is firm from the top.

ニーダ−中に存在するグリ−に9ン水を経時的にとυ、
その中Oグリセリン濃度を測定した。
Adding 9 ml of water to the greens present in the kneader over time,
The O-glycerin concentration therein was measured.

その結果は下記C)Mlである。The result is C) Ml below.

経過時間(分)  グリセリン濃度(%)l Q   
     12.8 20       13.5 30       15.6 実施例1 染色廃水の処理 TOC約8000 p、p、mの暗赤色の染料合成工場
の廃水を予め50〜55℃、40 r、p、mにて混練
中の60/80アス−7アルト1500 grに上部蓋
を外しニーダーの混線面がみえる状況の下で、徐々に添
加し混練した。(ニーダ−は内容5tである) 染料廃水はアスファルFを新たKかえることなしに何れ
の場合も100’OC宛4゛5分間処理し液をニーダ−
中よ〉取出し液量並びにTOCを測定した。
Elapsed time (minutes) Glycerin concentration (%) Q
12.8 20 13.5 30 15.6 Example 1 Treatment of dyeing wastewater Dark red dye synthesis factory wastewater with a TOC of approximately 8000 p, p, m was preliminarily treated at 50-55°C and 40 r, p, m. The mixture was gradually added to 1500 gr of 60/80 As-7 Alto during kneading and kneaded with the top cover removed so that the mixed wire surface of the kneader could be seen. (The content of the kneader is 5 tons.) In each case, the dye wastewater was treated with Asphal F for 4 to 5 minutes at 100'OC without changing it, and the liquid was transferred to the kneader.
Medium> The amount of liquid taken out and the TOC were measured.

その結果を次に示す。The results are shown below.

ム 処理廃液量(ロ)   TC)C(p、p、m)1
   400      4800 2   350      7000 3   500    、   56004   40
0      8000 5      400          62006
     350          56007  
   400         80008     
500         67009     450
          700010     350 
        6900処理廃波量はニーダ−をバッ
チIIKで利用しているため着千のバラツキ社あるが約
5001〜600W’lD水が失われて−るふ水分参−
去畜れているに屯か−わらず、TOCが減少しているの
は溶質が高粘弾性体に歌着Ik*されたためである。
M Processed waste liquid amount (b) TC) C (p, p, m) 1
400 4800 2 350 7000 3 500, 56004 40
0 8000 5 400 62006
350 56007
400 80008
500 67009 450
700010 350
The amount of waste wave processed by 6900 varies by a thousand because the kneader is used in batch IIK, but approximately 5001 to 600 W'1D water is lost.
The reason why the TOC decreases regardless of whether the livestock is shed is because solutes are absorbed into the highly viscoelastic body.

実施例4 染料廃水の処1 実施例3に示したと興じ実験でニーダ−の上部に透明の
ポリエチレンll0IIをしWk*された水が還流しニ
ーダ−中に戻ゐ様にした。
Example 4 Treatment of dye wastewater 1 In an experiment similar to that shown in Example 3, transparent polyethylene 110II was placed on the top of the kneader so that the Wk* water refluxed and returned to the kneader.

その結果上蓋に多量の水滴が付着し、この水は無色透明
であった。亦こOII置に依シ水OYスバランスはとれ
た。
As a result, a large amount of water droplets adhered to the top lid, and this water was clear and colorless. In addition, I was able to maintain a good balance between OII and OY.

更らKこの上蓋の横wに対称的な位置に2つの穴をあけ
一方より30℃に予め温−さ豐た空気を50jy/mi
nの量で通し、他方O大よシ空気を排出させた。この$
45t:で水の#出量社650鑑でありた。
Furthermore, two holes were made at symmetrical positions on the side of this top cover, and air preheated to 30℃ was pumped through one side at a rate of 50jy/mi.
The air was passed through in an amount of n, and on the other hand, air was expelled in an amount of o. This $
45t: It was #Izuresha 650 book of water.

夾#例& 汚泥の処1 活性汚泥(含水率85襲)中に生石[2%加え、これを
ニーダ−中當温で混IIIIifがみえる機にして混合
した。この場合ニーダ−は大気中沢開放された状態であ
る。この混合物社当初高−粘性を1つ黄褐色の混練体で
あるが徐klll(粘性を増し遂には禍1色が檜薄<′
fk!)もろ〈1kgて摩た。この状態での含水率a6
2囁であ伽威崖が可能である。
Examples & Sludge Process 1 2% raw stone was added to activated sludge (moisture content: 85%), and this was mixed in a kneader at a temperature of about 100°C until the mixture was visible. In this case, the kneader is open to the atmosphere. This mixture initially had a high viscosity and was a yellow-brown kneaded body, but it gradually increased in viscosity and finally turned into a yellow-brown kneaded body.
fk! ) Moro〈1kg and polished. Moisture content a6 in this state
It is possible to make a cliff with 2 whispers.

実施例6 ゼラチン水溶液の皓聰 ゼラチン水溶液を濃−することは、ゼラチンに要求され
る物性上系を高@にすること社出来ないので必ずしも容
易では1に−0 予め10%ゼラチン含有水溶液を30’C虻て40 r
、p、m =−グー中で30分関混線画がみえる程度の
流量で混練した。この際の(ラチン濃度F116%にな
った。
Example 6 Concentration of gelatin aqueous solution Concentrating gelatin aqueous solution is not always easy as it is not possible to increase the physical properties required for gelatin. 'C 40 r
, p, m = - The mixture was kneaded for 30 minutes at a flow rate at which a cross line pattern was visible. At this time (latin concentration F116%).

Claims (1)

【特許請求の範囲】 高粘弾性体中にl11掖(懸− 筐を含を、以下同様)を加え混練し、溶液中よ少溶媒(
分散媒を含む、以下同様]を***する方法。
[Claims] Add and knead 11 liters (including a suspension case, the same shall apply hereinafter) to a highly viscoelastic body, and add a small amount of solvent (
A method of *** including a dispersion medium, the same applies hereinafter].
JP9861381A 1981-06-24 1981-06-24 Removing method for solvent in solution and suspension Granted JPS58202A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9861381A JPS58202A (en) 1981-06-24 1981-06-24 Removing method for solvent in solution and suspension

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9861381A JPS58202A (en) 1981-06-24 1981-06-24 Removing method for solvent in solution and suspension

Publications (2)

Publication Number Publication Date
JPS58202A true JPS58202A (en) 1983-01-05
JPH0333361B2 JPH0333361B2 (en) 1991-05-16

Family

ID=14224429

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9861381A Granted JPS58202A (en) 1981-06-24 1981-06-24 Removing method for solvent in solution and suspension

Country Status (1)

Country Link
JP (1) JPS58202A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0251469A2 (en) * 1986-05-20 1988-01-07 Satake Technology Research And Development Associates Inc. Method for converting substances

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57171401A (en) * 1981-04-16 1982-10-22 Cosmo Co Ltd Treatment of aqueous solution of high molecular substance
JPS5844008A (en) * 1981-09-08 1983-03-14 株式会社東京タツノ Commodity display shelf

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57171401A (en) * 1981-04-16 1982-10-22 Cosmo Co Ltd Treatment of aqueous solution of high molecular substance
JPS5844008A (en) * 1981-09-08 1983-03-14 株式会社東京タツノ Commodity display shelf

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0251469A2 (en) * 1986-05-20 1988-01-07 Satake Technology Research And Development Associates Inc. Method for converting substances

Also Published As

Publication number Publication date
JPH0333361B2 (en) 1991-05-16

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