JPH01231909A - Antifoaming agent and antifoaming process - Google Patents

Antifoaming agent and antifoaming process

Info

Publication number
JPH01231909A
JPH01231909A JP5627888A JP5627888A JPH01231909A JP H01231909 A JPH01231909 A JP H01231909A JP 5627888 A JP5627888 A JP 5627888A JP 5627888 A JP5627888 A JP 5627888A JP H01231909 A JPH01231909 A JP H01231909A
Authority
JP
Japan
Prior art keywords
antifoaming
foam
compd
antifoaming agent
compound
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
JP5627888A
Other languages
Japanese (ja)
Other versions
JPH0349605B2 (en
Inventor
Ryozo Kurita
良造 栗田
Yoshiharu Yasuhara
義晴 安原
Katsuhiko Takahara
高原 勝彦
Takashi Tanaka
多加志 田中
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.)
NIKKA CHEM CO Ltd
Ebara Corp
Nikka Chemical Industry Co Ltd
Ebara Research Co Ltd
Original Assignee
NIKKA CHEM CO Ltd
Nikka Chemical Industry Co Ltd
Ebara Research Co Ltd
Ebara Infilco Co Ltd
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 NIKKA CHEM CO Ltd, Nikka Chemical Industry Co Ltd, Ebara Research Co Ltd, Ebara Infilco Co Ltd filed Critical NIKKA CHEM CO Ltd
Priority to JP5627888A priority Critical patent/JPH01231909A/en
Publication of JPH01231909A publication Critical patent/JPH01231909A/en
Publication of JPH0349605B2 publication Critical patent/JPH0349605B2/ja
Granted legal-status Critical Current

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Abstract

PURPOSE:To carry out biological treatment safely and to improve foam breaking effect and antifoaming effect remarkably by using an antifoaming agent obtd. by combining a specified addition product of glycol with an esterified product thereof. CONSTITUTION:An antifoaming agent is obtd. from a mixture consisting of a compd. expressed by formula I and a compd. expressed by formula II and/or III, and regulating a proportion of the compd. II and/or the compd. III to 5-55wt.%. In formulas, (l) is an integer 0-30; (m) is an integer 10-100; (n) is an integer 0-50; R1 is 17C alkyl group, alkenyl group; when >=2 alkylene oxide groups are present, the compd. is a block or random addition product. The antifoaming agent is used more effectively if it is added to an easily foaming liquid when the foam surface reaches at the set position while detecting the surface.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は新規な消泡剤及び消泡方法に関するもので17
、特にし尿処理施設の生物処理工程で発生する泡の障害
に対して、低象加率で効果的な破泡及び抑泡作用を発揮
する消泡沖J及び消泡方法に関するものでりる。
[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to a novel antifoaming agent and a novel antifoaming method.
The present invention relates to defoaming Oki J and a defoaming method that exhibit effective foam-breaking and foam-inhibiting effects with a low contamination rate, particularly against foam failures generated in the biological treatment process of human waste treatment facilities.

〔従来の技術〕[Conventional technology]

し尿処理施設における生物処理工程では、季節によシ処
塩遺及び負のな変動が大きく、運転操作条件などによっ
ては泡が大量に発生し、操作上大きなトラブルを生じ、
運転が困難となるケースがみられる。
In the biological treatment process at human waste treatment facilities, the amount of salt left behind varies greatly depending on the season, and depending on the operating conditions, a large amount of foam may be generated, causing major operational troubles.
There are cases where driving becomes difficult.

特に、最近のし尿処理施設では、希釈水が不要であう、
設置スペースが小であり、且つ維持管理費の大幅な削減
などの特長を有する無希釈高負荷処理を採用する例が増
加しつ〜あるが、この方式は従来とくらべて生物処理工
程(ばつき慴)で発泡しやすい11.JI向がみられる
In particular, recent human waste treatment facilities do not require dilution water.
More and more cases are being adopted of non-dilution, high-load treatment, which requires a small installation space and significantly reduces maintenance and management costs. 11. JI direction is seen.

これらし尿処理1s設から発生する泡に対して、破泡及
び抑泡の目的で、品枯アルコール脂肪酸エステル、シリ
コーン、釜稿石けん、鉱物油、ハーフエステル寺の化合
物が単独で又は2棟以上配合され、消泡剤として処理状
況にふ−6じて各々便用されている。
For the foam generated from these human waste treatment facilities, one or more compounds such as dry alcohol fatty acid ester, silicone, kamako soap, mineral oil, and half ester are added for the purpose of foam breaking and foam suppression. They are used as antifoaming agents depending on the processing situation.

一般に界面活性剤と會む消泡剤としては11)  高級
アルコールにプロピレンオキサイド、エチレンオキサイ
ドを付加した消泡剤。
Antifoaming agents that generally interact with surfactants include 11) Antifoaming agents with propylene oxide and ethylene oxide added to higher alcohols.

(2)  高級脂肪酸のエチレンオキサイド付加物の高
級脂肪酸エステル、又は高級脂肪酸のグロビレンオキサ
イド付/JO物の高級脂肪酸エステル金含む消泡剤。
(2) An antifoaming agent containing gold, a higher fatty acid ester of an ethylene oxide adduct of a higher fatty acid, or a higher fatty acid ester of a higher fatty acid with globylene oxide/JO product.

などがある。and so on.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

前に述べた無希釈高負荷処理の場合、処理上、はつき槽
汚泥を高濃度に維持しなければならないため、槽内は篩
水温で発泡しやすい条件下にろる。これらの発泡障害に
対して、い1Nで使用されていた消泡剤は破泡及び抑泡
効果が十分とは言えず、状況に応じて便用虜を増大し、
対処する必要があった。
In the case of the above-mentioned non-dilution, high-load treatment, the sludge in the sieving tank must be maintained at a high concentration, so the sieve water temperature creates conditions in the tank that make it easy to foam. To deal with these foaming problems, the antifoaming agent used in I1N cannot be said to have sufficient foam-breaking and foam-inhibiting effects, and depending on the situation, the defoaming agent may be increased.
It needed to be addressed.

しかしながら、し尿処理施設の場合、生物処理という制
約された条件ドで使用するため、用いら扛る消泡剤は処
理上、悪影響ケ及ぼさず、しかも安1曲で潰れた消泡効
果を自゛することが資求される。
However, in the case of human waste treatment facilities, the antifoaming agents used do not have a negative effect on the treatment because they are used under the restricted conditions of biological treatment, and moreover, the antifoaming agent that is used does not have a negative effect on the treatment, and moreover, the antifoaming agent that is used in the treatment facility loses its antifoaming effect. You are required to do so.

前に挙けた単独、又は2株以上の配合物よりなる消泡剤
はその用途に応じてすぐれた機能金有するか、し尿処理
施設向の消泡剤に限り′fc、場合、いくつかの欠点が
ある。
The antifoaming agents listed above, either singly or as a combination of two or more, may have excellent functionality depending on the application, or may have some drawbacks if they are limited to antifoaming agents for human waste treatment facilities. There is.

列えば、シリコーン系化合物では速効性、持続性ともに
十分でなく、シかも沈殿池などの内壁にシリコンオイル
が付層残留し、後処理が必要となること、又、鉱物油系
では遊離した油が生物処理の処理阻害とな9、機能低下
につながるなどトラブルの原因となっている。
For example, silicone-based compounds do not have sufficient fast-acting or long-lasting properties, and may leave a layer of silicone oil on the inner walls of sedimentation tanks, requiring post-treatment.Also, mineral oil-based compounds do not release free oil. This causes problems such as inhibiting biological treatment9 and leading to functional decline.

一方、合成された界面活性剤系消泡剤ではその種類、形
態、プロピレンオキサイドやエチレンオキサイドの付カ
ロモル数、組合せなどにより破泡及び抑泡効果はそれぞ
れ異なシ、速効性、持続性などに問題がめった。
On the other hand, the foam-breaking and foam-inhibiting effects of synthesized surfactant-based antifoaming agents vary depending on their type, form, number of calomoles of propylene oxide and ethylene oxide, and combinations, etc., and there are problems with quick-acting, sustainability, etc. I was disappointed.

特に、し尿処理施設から発生する発泡成分は活性汚泥に
吸着、濃縮された物實、例えば活性汚泥の中の菌体外ポ
リマーに起因していると考えられ、泡自体粘7W性が極
めて高く、消泡には大量の薬剤を必要とした。
In particular, the foaming components generated from human waste treatment facilities are thought to be caused by substances adsorbed and concentrated in activated sludge, such as extracellular polymers in activated sludge, and the foam itself has extremely high viscosity. A large amount of chemicals were required to defoamer.

本発明者らは、このような従来技術における問題点全解
決すべく杜々検討金行つfc結果、生物処理に安全でし
かも[泡および抑泡効果共に優れた自己乳化型のiIr
規な消泡剤を見いだすに到った。
The inventors of the present invention have made extensive studies to solve all of the problems in the conventional technology, and as a result, we have developed a self-emulsifying type iIR that is safe for biological treatment and has excellent foam and foam-inhibiting effects.
We have discovered a standard antifoaming agent.

〔問題点を解決するための手段〕[Means for solving problems]

本発明は、 一般式 %式% (但し、式中lはO〜30、mは10〜100、nは0
〜50の整数を表わし、R4はC17のアルキル基又は
アルケニル基を示し、上記アルキレンオキサイド基が2
棟以上存在する場合には、ブロック又はランタム付加体
で必る。) で表わされる化合物Iと化合物菖及び/又は化合物温と
の混合物よりなり、該混合物に対する化合物置及び/又
は化合物置の配合割合が10〜50皿虚%であることを
特徴とする消泡〈1j0及び011記消泡ハリ全発泡性
液体に泳加するに際し、設足した泡面位14?検知する
ことによって前記消泡材t−伶加すること全特徴とする
消泡方法である。
The present invention is based on the general formula % formula % (wherein l is 0 to 30, m is 10 to 100, and n is 0
represents an integer of ~50, R4 represents a C17 alkyl group or alkenyl group, and the alkylene oxide group is 2
If there are more than one ridge, it must be a block or a random adduct. ) An antifoaming agent consisting of a mixture of compound I represented by the formula I and compound iris and/or compound tsun, characterized in that the blending ratio of the compound holder and/or compound holder to the mixture is 10 to 50 percent. 1j0 and 011 Defoaming tension When adding to the foaming liquid, the foam surface level 14? This defoaming method is characterized in that the defoaming material is added by detection.

本発明においては、lが30より大きくなると親水江が
大となり、常温において町m化状態となシ消泡力は著し
く低下する。
In the present invention, when l is larger than 30, the hydrophilicity becomes large and the defoaming power becomes extremely low at room temperature.

また、m及びnが夫々100及び50より大きい場合に
は親油性が増大し、自己乳化性及び拡散性か悪くなる。
Furthermore, when m and n are larger than 100 and 50, respectively, lipophilicity increases and self-emulsifying property and diffusibility become worse.

一数式厘及び鳳で示される化合物のR1はC17H55
−のアルキル基又はアルケニル基を示し、これ以外のも
のでは好1しくない。
R1 of the compound represented by Issakurin and Otori is C17H55
- represents an alkyl group or an alkenyl group, and other groups are not preferred.

例えばR1の炭素数が016 以下の場合には消泡力か
弱く、逆に018以上の場合には自己乳化性が悪くなる
For example, if the number of carbon atoms in R1 is 016 or less, the antifoaming power will be weak, and if it is more than 018, the self-emulsifying property will be poor.

又、消泡剤中における一数式…及び/又は層で示される
化合物の配合割合は10〜50嵐敏%が最も好1しく、
このが1合で配合した場合に破泡及び抑泡作用において
顕著な効果を示す。
In addition, the compounding ratio of the compound represented by formula 1 and/or layer in the antifoaming agent is most preferably 10 to 50% Arashimin.
When blended in one portion, it exhibits remarkable effects on foam-breaking and foam-inhibiting effects.

本発明の消泡剤は、その1へ原液の形で使用しても水に
乳化させて使用しても性能はかわらない。又、溶剤等と
混合して使用しても購わない。
The antifoaming agent of the present invention has the same performance whether it is used in the form of a stock solution or emulsified in water. Also, do not use it if mixed with solvents, etc.

本発明の消泡剤は101ψ/に〜30〜/lの割合にな
るように被処理故に添加すればよい。
The antifoaming agent of the present invention may be added at a ratio of ~30~/l to 101ψ/l to be treated.

本発明で用いる一般式Iで示される化合物は、エチレン
グリコール、グロピレングリコール及び/又はブチレン
ゲリール等全アルカリ触媒の存在下に付加反応を行わせ
ることによりs造することができる。
The compound represented by the general formula I used in the present invention can be prepared by carrying out an addition reaction in the presence of an all-alkaline catalyst such as ethylene glycol, glopylene glycol and/or butylene gelyl.

一方、−数式鳳及び烏で示1れる化合物は、上記方法で
得られた一数式■で示される化合物ト、ハラトルエンス
ルフォン酸等のエステル化触媒の存在下に1w1級脂肪
酸とのエステル化反応により、或いは尚縁側肪酸クライ
トとの脱塩酸反工6によシ或いは低級アルコール尚M脂
肪fソエステルを用いてエステル交換反応によっても得
ることができる。
On the other hand, the compounds represented by formulas 1 and 1 obtained by the above method undergo an esterification reaction with 1w primary fatty acids in the presence of an esterification catalyst such as halatoluenesulfonic acid. Alternatively, it can be obtained by a dehydrochlorination reaction with a fatty acid chloride, or by transesterification using a lower alcohol ester.

又尚截加肪峨に直接アルキレンオキサイド全付加反応さ
せることにより目的物音イすることもできる。
It is also possible to produce the desired substance by directly carrying out a total addition reaction with alkylene oxide.

また、前記消泡材を用いる消泡方法は、し原券の発泡性
g!i、体を生物処理して発泡が起きたら龜〃口するか
、適宜位置に框極寺の検升器紫設け、泡面が設定位置に
達したのゲ検知したら添加するように制御するのが好ま
しい。
In addition, the defoaming method using the defoaming material described above is based on the foaming property of the original note. i. When the body is biologically treated and foaming occurs, add the foam, or set up a tester at the appropriate location and control it so that it is added when the foam level reaches the set position. is preferred.

実施例 本発明の消泡剤と従来品の消泡効果について、以下の方
法を用いて比較検討を行った。
EXAMPLE The antifoaming effects of the antifoaming agent of the present invention and conventional products were compared and studied using the following method.

試験方法:試練装置は直径60φ、長す1000態の透
明アクリル製カラムを用い外側にはサンプル7fr株温
す/bため、直径100φ、長す800騙の透明アクリ
ル候カラム全温水用ジーYケットとして設けた。
Test method: The test equipment is a transparent acrylic column with a diameter of 60φ and a length of 1000 mm, and a transparent acrylic column with a diameter of 100φ and a length of 800 mm on the outside to heat the sample 7 fr/b. It was established as

ばつさはカラム底部に設けた散気法から空気を送り出す
デフィーザ・ストーン法を採用した。
Batsusa adopted the defeaser stone method, which pumps out air through a diffuser installed at the bottom of the column.

試験にあたっては、サンプルを一定数の空気で1〜2分
間ばつさし、光重しfc泡を一定の高さに調整したの5
1ばつ@を停止し、消泡剤上池の狭面に絡〃口し、泡の
消滅状況t−副定した(破泡効果)。更に、泡消滅後、
再度一定量の空気でばつさ紫行い、ばつき直後から8分
区まで経時的に泡の高さを測定した。(抑泡効果)。
For the test, the sample was exposed to a certain number of air for 1 to 2 minutes, and the FC bubble was adjusted to a certain height using a light weight.
The bubble was stopped, the antifoam was applied to the narrow side of the upper reservoir, and the state of disappearance of bubbles (t) was determined (bubble breaking effect). Furthermore, after the bubbles disappear,
Bubble foaming was performed again using a fixed amount of air, and the height of the bubbles was measured over time from immediately after the flashing to the 8th section. (foam suppressing effect).

以上、破泡及び抑泡効果よシ谷哨帛削の効能について、
唸合的な評価を行った。
The above is about the foam breaking and foam suppressing effects as well as the effectiveness of valley guard removal.
We conducted a comprehensive evaluation.

(1)対象試料:無希釈高負荷処理ばつき槽汚泥(2)
  供試試量:1p (3)  ばつき空気量:2e/分 (4)  消1’@!剤fE人率: 10 +n9 /
 (3供試消泡剤は発明品6種類、従来品4種類のft
 f O*で6り、#細な内容を表−1に示し、結果を
衣−2に示す。
(1) Target sample: Undiluted high-load treatment sludge from the dusting tank (2)
Test amount: 1p (3) Bumping air amount: 2e/min (4) Discharge 1'@! Agent fE person rate: 10 +n9 /
(3) The antifoaming agents tested were 6 types of invented products and 4 types of conventional products.
f O* is 6, #details are shown in Table 1, and the results are shown in Table 2.

表−3は無希釈高負荷処理施設において、本発明の消泡
剤と従来品の消泡効果について比較検討した結果である
Table 3 shows the results of a comparative study of the defoaming effects of the defoaming agent of the present invention and conventional products in a non-dilution, high-load processing facility.

試験では泡面計により泡の高さが一定レベルに保持でき
るよう注入ボング金ON −art運転しながら、原液
、又は水で50倍に希釈した消泡剤を注入した。
In the test, the antifoaming agent was injected as a stock solution or diluted 50 times with water while the injection bong metal ON-art was operated so that the height of the foam was maintained at a constant level using a foam level meter.

結果を表−3に示す。The results are shown in Table-3.

その結果、本発明品を通用した場合、希釈注入法では就
米品に対して2.6倍、原液注入法では1.7倍消泡効
釆がすぐれてお夛、従来品とくらべて約40〜b 果が得られた。
As a result, when the product of the present invention is used, the antifoaming effect is 2.6 times better than that of the American product when using the diluted injection method, and 1.7 times more effective when using the undiluted solution method, and approximately 100 times more effective than the conventional product. 40-b fruit was obtained.

合物との混合物を用いた場合にも同様の効果が得られる
A similar effect can be obtained when a mixture with a compound is used.

〔発明の効果〕〔Effect of the invention〕

以上、詳述したように本発明品の消泡剤は次のようなす
ぐれた効果を有するものである。
As detailed above, the antifoaming agent of the present invention has the following excellent effects.

(l)シ尿処fi施設はつII為ら発生する泡の障害に
対して、速効性(破泡作用)、持続性(抑泡作用)とも
にすぐれており、少量の添加濾で安定した処理が期待で
きる。
(l) Excellent fast-acting (foam-breaking effect) and long-lasting (foam-inhibiting effect) against foam problems caused by urinary treatment facilities, and stable treatment with a small amount of added filtration. can be expected.

(2)本発明品は乳化安定性がすぐれている次め、水で
希釈し、乳化状態で使用してもみ敵注入法と伺ら差異は
なく、性能上、特に問題はない。
(2) The product of the present invention has excellent emulsion stability, and when it is diluted with water and used in an emulsified state, there is no difference from the kneading injection method, and there are no particular problems in terms of performance.

(3)  本発明品は装置および機器に対し、残留物に
よる付漕がなく、シかも生物処理の処理阻害となる女囚
がないので、長期間継続使用しても処理上、特に問題は
ない。
(3) The product of the present invention does not cause residues to accumulate on the equipment and equipment, and there are no female prisoners that may impede biological treatment, so there are no particular problems in treatment even if it is used continuously for a long period of time.

特許出願人 荏原インフィルコ株式会社同    株式
会社 荏原総合研究所 同   日華化学工業株式会社
Patent applicant Ebara Infilco Co., Ltd. Ebara Research Institute Co., Ltd. NICCA Chemical Industry Co., Ltd.

Claims (1)

【特許請求の範囲】 1、一般式 HO−〔(C_2H_4O)_l−(C_3H_6O)
_m−(C_4H_8O)_n〕H… I ▲数式、化学
式、表等があります▼…II ▲数式、化学式、表等があります▼…III (但し、式中lは0〜30、mは10〜100、nは0
〜50の整数を表わし、 R_1はC_1_7のアルキル基又はアルケニル基を示
し、上記アルキレンオキサイド基が2種以上存在する場
合には、ブロック又はランダム付加体である。) で表わされる化合物 I と化合物II及び/又は化合物II
Iとの混合物よりなり、該混合に対する化合物II及び/
又は化合物IIIの配合割合が5〜55重量%であること
を特徴とする消泡剤。 2、特許請求の範囲第1項記載の消泡剤を発泡性液体に
添加するに際し、設定した泡面位置を検知することによ
つて前記消泡材を添加することを特徴とする消泡方法。
[Claims] 1. General formula HO-[(C_2H_4O)_l-(C_3H_6O)
_m-(C_4H_8O)_n〕H...I ▲There are mathematical formulas, chemical formulas, tables, etc.▼...II ▲There are mathematical formulas, chemical formulas, tables, etc.▼...III (However, in the formula, l is 0 to 30 and m is 10 to 100. , n is 0
It represents an integer of ~50, R_1 represents an alkyl group or alkenyl group of C_1_7, and when two or more types of the above alkylene oxide groups are present, it is a block or random adduct. ) Compound I and compound II and/or compound II represented by
I, and the compound II and/or
Or an antifoaming agent characterized in that the blending ratio of compound III is 5 to 55% by weight. 2. A defoaming method characterized in that when adding the defoaming agent according to claim 1 to a foaming liquid, the defoaming agent is added by detecting a set foam surface position. .
JP5627888A 1988-03-11 1988-03-11 Antifoaming agent and antifoaming process Granted JPH01231909A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5627888A JPH01231909A (en) 1988-03-11 1988-03-11 Antifoaming agent and antifoaming process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5627888A JPH01231909A (en) 1988-03-11 1988-03-11 Antifoaming agent and antifoaming process

Publications (2)

Publication Number Publication Date
JPH01231909A true JPH01231909A (en) 1989-09-18
JPH0349605B2 JPH0349605B2 (en) 1991-07-30

Family

ID=13022622

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5627888A Granted JPH01231909A (en) 1988-03-11 1988-03-11 Antifoaming agent and antifoaming process

Country Status (1)

Country Link
JP (1) JPH01231909A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011083715A (en) * 2009-10-16 2011-04-28 San Nopco Ltd Defoaming agent
JP2017202461A (en) * 2016-05-12 2017-11-16 サンノプコ株式会社 Defoaming agent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011083715A (en) * 2009-10-16 2011-04-28 San Nopco Ltd Defoaming agent
JP2017202461A (en) * 2016-05-12 2017-11-16 サンノプコ株式会社 Defoaming agent

Also Published As

Publication number Publication date
JPH0349605B2 (en) 1991-07-30

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