JPS6291230A - Reactor - Google Patents
ReactorInfo
- Publication number
- JPS6291230A JPS6291230A JP60231654A JP23165485A JPS6291230A JP S6291230 A JPS6291230 A JP S6291230A JP 60231654 A JP60231654 A JP 60231654A JP 23165485 A JP23165485 A JP 23165485A JP S6291230 A JPS6291230 A JP S6291230A
- Authority
- JP
- Japan
- Prior art keywords
- antifoaming agent
- reactor
- foam
- specimen
- antifoaming
- 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
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0006—Controlling or regulating processes
- B01J19/002—Avoiding undesirable reactions or side-effects, e.g. avoiding explosions, or improving the yield by suppressing side-reactions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/70—Mixers specially adapted for working at sub- or super-atmospheric pressure, e.g. combined with de-foaming
- B01F33/71—Mixers specially adapted for working at sub- or super-atmospheric pressure, e.g. combined with de-foaming working at super-atmospheric pressure, e.g. in pressurised vessels
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/00049—Controlling or regulating processes
- B01J2219/00245—Avoiding undesirable reactions or side-effects
- B01J2219/0025—Foam formation
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
この発明は反応液または処理液の発泡を抑制するための
反応装置に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a reaction apparatus for suppressing foaming of a reaction liquid or a treatment liquid.
従来、液体試料を処理する過程で発泡が起こり、泡が生
長して容器外にこぼれることを防ぐためには泡の発生を
検知し、試料液に適当な消泡剤全逐次添加するか、ある
込は予め発泡が起こらないように所定の濃度に消泡剤を
添加することが行われていた。Conventionally, foaming occurs during the process of processing liquid samples, and in order to prevent the foam from growing and spilling out of the container, it is necessary to detect the occurrence of foam and add an appropriate antifoaming agent to the sample liquid sequentially, or to prevent the foam from growing and spilling out of the container. In order to prevent foaming, an antifoaming agent was added to a predetermined concentration in advance.
しかしこのような従来の方法によっては、消泡剤の添加
量は必ず過剰となる欠点があった。多くの消泡剤を逐次
添加する場合には、一般的に添加のたびに消泡効果が小
さくなる傾向があり、添加の頻度は一処理工程で初期に
比べ終期はど大きくなり、終には大過剰の添加に至るケ
ースがあり、消泡剤の節約ができないばかりでなく試料
中に不必要な消泡剤成分を不本意に蓄積するという問題
が起こっていた。However, such conventional methods have the disadvantage that the amount of antifoaming agent added is always excessive. When many antifoaming agents are added sequentially, the antifoaming effect generally tends to decrease with each addition, and the frequency of addition is greater at the end than at the beginning in one treatment process; In some cases, a large excess of antifoaming agent was added, which not only made it impossible to save on the antifoaming agent, but also resulted in the problem of undesirably accumulating unnecessary antifoaming agent components in the sample.
本発明は消泡剤の過剰供給全防止することを目的とした
反応装置を提供するものである。The present invention provides a reaction apparatus aimed at completely preventing excessive supply of antifoaming agent.
本発明は反応液を充填した反応槽内の液面上方に消泡剤
を保持する構造体を設置したことを特徴とする反応装置
である。The present invention is a reaction apparatus characterized in that a structure for holding an antifoaming agent is installed above the liquid level in a reaction tank filled with a reaction liquid.
本発明の装置を用いると生長する泡は液面上に保持され
た消泡剤に触れるやいなや、泡は完全に消える。触れる
ことによって消費される消泡剤は不思議なことに液中に
添加する場合に比べ極めて少量でよい、再度生長する泡
も同様にして消泡できる。With the device of the invention, as soon as the growing foam touches the antifoam agent held above the liquid surface, the foam disappears completely. Curiously, only a small amount of antifoaming agent is consumed by contact, compared to when it is added to the liquid, and foam that grows again can be defoamed in the same way.
尚、消泡剤を保持する構造体としては、例えば消泡剤を
多孔性物体に含ませたもの、あるいは浅い皿状の容器に
消泡剤を入れ、これを液面上に保持する構造でもよい。The structure for holding the antifoaming agent may be, for example, one in which the antifoaming agent is contained in a porous object, or a structure in which the antifoaming agent is placed in a shallow dish-shaped container and held above the liquid surface. good.
以上のように本発明装置によれば消泡剤は過剰に添加さ
れることがなく、このため必要以上に試料中に消泡剤が
混入する心配もなくなる。これは発生する表面張力の小
さい泡が種々の形で保持された消泡剤成分に接触するや
いなや小量とはいえ効果的に泡全体に消泡剤が広がるこ
とになり、液体中に余分に加えられることとは異なる効
果が期待できるものと考えられ、したがって、消泡剤の
無駄な消費を抑え、あわせて消泡剤の蓄積をなくすこと
ができる効果を有する。As described above, according to the apparatus of the present invention, an excessive amount of antifoaming agent is not added, and therefore there is no fear that more antifoaming agent will be mixed into the sample than necessary. This means that as soon as the generated foam with a low surface tension comes into contact with the antifoam component held in various forms, the antifoam agent will effectively spread throughout the foam, albeit in a small amount, and excess It is thought that a different effect can be expected from adding the antifoaming agent, and therefore, it has the effect of suppressing wasteful consumption of the antifoaming agent and also eliminating accumulation of the antifoaming agent.
以下に本発明の実施例を示す。 Examples of the present invention are shown below.
オレイン酸ノーダヲ0.01ts含む試料水中の第一鉄
イオンを空気酸化するため、第1図に示す本発明の反応
装置を用いた。直径18cIrLの円筒形の反応槽lの
底部に濾過板を設け、これを通して3ノの試料2を入れ
αir f毎分31の割合でパイプ10より供給した。The reaction apparatus of the present invention shown in FIG. 1 was used to air oxidize ferrous ions in sample water containing 0.01 ts of oleic acid. A filtration plate was provided at the bottom of a cylindrical reaction tank 1 with a diameter of 18 cIrL, through which 3 samples 2 were introduced and supplied from a pipe 10 at a rate of 31 αirf/min.
一方、液面3より上方10cIILに有機シリコン系消
泡剤クリレスS 1015 K−入れた容[50偲の容
器6t−保持し、この上にウレタンフオームのカバー7
を行った。酸化反応を続ける間泡4の高さHに時間とと
もに第2図のように変化し、最大高さAは第1図の9の
水準に維持されたが1時間の酸化反応中に反応系に移行
した消泡剤全濃度で示すと20 r!?’l以下であっ
た。この装置を用いると泡が反応装置の上端8から溢れ
たり吹きこぼれることはなかった。On the other hand, a 6 ton container containing the organosilicon antifoaming agent Kuriles S 1015 K (50 m) was placed 10 cIIL above the liquid level 3, and a urethane foam cover 7 was placed on top of the container.
I did it. While the oxidation reaction continued, the height H of the bubbles 4 changed over time as shown in Figure 2, and the maximum height A was maintained at the level 9 in Figure 1, but during the oxidation reaction for 1 hour, the height H of the bubbles 4 changed as shown in Figure 2. The total concentration of antifoam transferred is 20 r! ? 'l or less. Using this device, bubbles did not overflow or boil over from the top 8 of the reactor.
(比較例)
消泡剤を液面上に保持せず、消泡剤を直接滴下すること
以外は実施例と同じ反応を行ったところ、1時間に20
回以上添加しなければならず、ややもすると吹きこぼれ
が生じた。さらに消泡剤の消費量からみかけの添加濃度
を計算すると300 m9711以上となり、添加効果
は段々小さくなった。(Comparative example) The same reaction as in the example was carried out except that the antifoaming agent was not held on the liquid surface and the antifoaming agent was directly dropped.
It had to be added more than once, and boiling over occurred after a while. Furthermore, when the apparent addition concentration was calculated from the amount of antifoaming agent consumed, it was over 300 m9711, and the addition effect gradually became smaller.
以上、具体的に示したように本発明の反応装置の効果は
明らかである。As specifically shown above, the effects of the reaction apparatus of the present invention are clear.
第1図は本発明の一実施例を示す断面図、第2図は泡の
高さの時間的変化を示す図である。
1・・・反応槽、2・・・試料、3・・・液面、4・・
・泡、5・・・消泡剤、6・・・容器
特許出願人 日本電気株式会社
代 埋 入 弁理士 内 原 晋 ノ゛゛第1
図
手2図FIG. 1 is a sectional view showing an embodiment of the present invention, and FIG. 2 is a diagram showing temporal changes in bubble height. 1... Reaction tank, 2... Sample, 3... Liquid level, 4...
・Foam, 5... Antifoaming agent, 6... Container Patent applicant: NEC Corporation Patent attorney: Susumu Uchihara No. 1
Figure 2
Claims (1)
を保持する構造体を設置したことを特徴とする反応装置
。(1) A reaction device characterized in that a structure for holding an antifoaming agent is installed above the liquid level in a reaction tank filled with a reaction liquid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60231654A JPS6291230A (en) | 1985-10-16 | 1985-10-16 | Reactor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60231654A JPS6291230A (en) | 1985-10-16 | 1985-10-16 | Reactor |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6291230A true JPS6291230A (en) | 1987-04-25 |
JPH0149536B2 JPH0149536B2 (en) | 1989-10-25 |
Family
ID=16926878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60231654A Granted JPS6291230A (en) | 1985-10-16 | 1985-10-16 | Reactor |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6291230A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009046333A (en) * | 2007-08-16 | 2009-03-05 | Seiko Instruments Inc | Hydrogen generating apparatus and fuel cell system |
-
1985
- 1985-10-16 JP JP60231654A patent/JPS6291230A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2009046333A (en) * | 2007-08-16 | 2009-03-05 | Seiko Instruments Inc | Hydrogen generating apparatus and fuel cell system |
Also Published As
Publication number | Publication date |
---|---|
JPH0149536B2 (en) | 1989-10-25 |
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