JPS6238208A - Waste water treatment agent - Google Patents

Waste water treatment agent

Info

Publication number
JPS6238208A
JPS6238208A JP17613485A JP17613485A JPS6238208A JP S6238208 A JPS6238208 A JP S6238208A JP 17613485 A JP17613485 A JP 17613485A JP 17613485 A JP17613485 A JP 17613485A JP S6238208 A JPS6238208 A JP S6238208A
Authority
JP
Japan
Prior art keywords
acid
treatment agent
oil
radical
waste 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
JP17613485A
Other languages
Japanese (ja)
Other versions
JPH0225646B2 (en
Inventor
Kenji Uemura
健治 植村
Yasuaki Ogawa
小川 康昭
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.)
New Japan Chemical Co Ltd
Original Assignee
New Japan Chemical 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 New Japan Chemical Co Ltd filed Critical New Japan Chemical Co Ltd
Priority to JP17613485A priority Critical patent/JPS6238208A/en
Publication of JPS6238208A publication Critical patent/JPS6238208A/en
Publication of JPH0225646B2 publication Critical patent/JPH0225646B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To remove almost oil content of oil-drop-in-water type emulsion and minimize the formation of scum by utilizing the waste water treatment agent having salt shown by the special constitutional formula as main component. CONSTITUTION:Salt shown by the following general formula (in the formula, R<1> is any one of alkyl radical, alkenyl radical, alalkyl radical, phenyl radical or cycloalkyl radical each with 6-20C, R<2> and R<3> are alkyl radical or alkenyl radical having hydrogen or 1-20C, and X is carboxylic acid or oxyacid) is used as waste water treatment agent under 100-1,000ppm, pH9 against waste water. The treatment agent is produced by neutralization reaction of primary, secondary, and tertiary amine on carboxylic acid and oxyacid.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は廃水処理剤、特に水中油滴型エマルションの油
水分離能を有する新規な廃水処理剤に関するものである
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The present invention relates to a wastewater treatment agent, particularly a novel wastewater treatment agent having the ability to separate oil and water from an oil-in-water emulsion.

[従来の技術] 現在、金属加工の分野において、引火しない、あるいは
べとつかない等の利点から水溶性の切削油の使用伍が年
々増加している。ところが、これらの廃水の処理はいま
だ完成されたとは言えない。
[Prior Art] Currently, in the field of metal processing, the use of water-soluble cutting oils is increasing year by year due to their advantages such as non-flammability and non-stick properties. However, it cannot be said that the treatment of these wastewaters has been completed yet.

現状では、硫酸パン士やポリ塩化アルミニウム等の無機
凝集剤とノニオン系の高分子凝集剤の併用により処理さ
れているが、1回の処理では充分な効果が得られず、2
〜3回同一の操作を繰り返さなければならない。そのた
め、このようにして回収されたスカムは串も多く、スカ
ム中の油分を除去した残渣が無機物であるため、燃焼し
た後の処理も新たな問題となってきている。その他、限
外濾過膜法等の膜処理によっても一部処理されているが
、廃水そのままでは油分が多く短時間で膜の性能が低下
するため、膜処理前にできるだけ廃水中の油分を除去す
ることが望まれている。
Currently, treatment is performed using a combination of inorganic flocculants such as sulfuric acid or polyaluminum chloride and nonionic polymer flocculants, but a single treatment does not provide sufficient effect, and two
The same operation must be repeated ~3 times. Therefore, the scum collected in this way has many skewers, and since the residue after removing the oil in the scum is an inorganic substance, the treatment after combustion has become a new problem. In addition, part of the treatment is carried out by membrane treatment such as ultrafiltration membrane method, but wastewater contains a lot of oil as it is and the performance of the membrane deteriorates in a short period of time, so it is necessary to remove as much oil as possible from wastewater before membrane treatment. It is hoped that

このような切削油廃水の他に、圧延工程より排出される
圧延油等の廃水も同様に微細な油分が多く分散しており
、同様な問題を抱えている。その他、水中油滴型エマル
ションとして船舶から排出されるビルジ水ヤバラスト水
についても、機械、部品等の洗浄に用いた洗剤等が混入
し、現状の分離機だ【プでは処理不可能な場合がおる。
In addition to such cutting oil wastewater, wastewater such as rolling oil discharged from the rolling process similarly has a large amount of fine oil dispersed therein, and has similar problems. In addition, bilge water and ballast water discharged from ships as an oil-in-water emulsion may be contaminated with detergents used for cleaning machinery, parts, etc., and cannot be treated with current separators. .

[発明が解決しようとする問題点] 本発明者らはこのような水中油滴型エマルション中の油
分のほとんどを除去することができ、かつスカムの生成
ヱの少ない処理剤を創出すべく鋭意検問した結果、ある
種の化合物を廃水中に少量添加して撹拌するだけで水中
の油分が浮上し、効率良く分離回収し得ることを児い出
し、この知見に基づいて本発明を完成した。
[Problems to be Solved by the Invention] The present inventors have conducted extensive research in order to create a processing agent that can remove most of the oil content in such oil-in-water emulsions and that produces less scum. As a result, they discovered that by simply adding a small amount of a certain compound to wastewater and stirring it, the oil in the water floats to the surface and can be efficiently separated and recovered.Based on this knowledge, the present invention was completed.

即も、本発明は、下記の一般式で表わされる塩を主成分
とする新規な廃水処理剤を提供することを目的とする。
An object of the present invention is to provide a novel wastewater treatment agent containing a salt represented by the following general formula as a main component.

R’ R2R3N−X (式中、R1は炭素数6〜20のアルギル基、アルケニ
ル基、アラルキル基、フェニル基又はシフ0アルキル基
て必り、R及びR3は水素若しくは炭素数1〜20のア
ルキル基、アルケニル基であり、Xはカルホン酸若しく
はオキシ酸を示T、>[問題を解決するための手段] 一般式において、R1は炭素数6〜20の直鎮状若しく
は分岐鎖状の、置換基を有していてもよいアルキル基、
アルケニル基、アラルキル基、フェニル基若しくはシク
ロアルキル基である。このような基としては、オクチル
、デシル、ウンデシル、ラウリル、1〜リゾシル、ミリ
スチル、パルミチル、ステアリル等のアルキル基、ドデ
セニル、オレイル、リルイル等のアルケニル基、ベンジ
ル、フェネチル、フェニルプロピル、フェニルブチル、
フェニルオクチル、フェニルセチル、フェニルオクタデ
シル等のアラルキル基、フェニル、ナフチル等のアリル
基、シクロヘキシル等のシフ0アルキル基が例示される
。又、R及σR3としては水素若しくは炭素数1〜20
のアルキル基、アルケニル基である。このような基とし
ては、メチル、エチル、プロピル、ブチル、ヘキシル、
2−エチルヘキシル、オクチル、デシル、ラウリル、ミ
リスチル、バルミヂル、ステアリル等のアルキル基、エ
チニル、アリール、ウンデセニル、オレイル、リルニル
等のアルケニル基か挙げられる。
R' R2R3N-X (wherein R1 is necessarily an argyl group, an alkenyl group, an aralkyl group, a phenyl group, or an alkyl group having 6 to 20 carbon atoms, and R and R3 are hydrogen or alkyl having 1 to 20 carbon atoms. group, alkenyl group, and X represents a carbonic acid or an oxyacid. an alkyl group which may have a group,
It is an alkenyl group, an aralkyl group, a phenyl group or a cycloalkyl group. Such groups include alkyl groups such as octyl, decyl, undecyl, lauryl, 1-lysosyl, myristyl, palmityl, and stearyl, alkenyl groups such as dodecenyl, oleyl, and lylyl, benzyl, phenethyl, phenylpropyl, phenylbutyl,
Examples include aralkyl groups such as phenyl octyl, phenyl cetyl and phenyl octadecyl, allyl groups such as phenyl and naphthyl, and alkyl groups such as cyclohexyl. In addition, R and σR3 are hydrogen or carbon atoms 1 to 20
is an alkyl group or an alkenyl group. Such groups include methyl, ethyl, propyl, butyl, hexyl,
Examples include alkyl groups such as 2-ethylhexyl, octyl, decyl, lauryl, myristyl, valmidyl, and stearyl, and alkenyl groups such as ethynyl, aryl, undecenyl, oleyl, and lylunyl.

カルボン酸としては、酢酸、プロピオン酸、酪酸、カプ
ロン酸、カプリル酸、ラウリル酸、ミリスチン酸、パル
ミチン酸、ステアリン酸、オレイン酸、安息香酸等の1
価カルボン酸、シュウ酸、マロン酸、コハク酸、アジピ
ン酸、フタル酸等の2価のカルボン酸、ヘミメリト酸、
トリメリット酸等の3価のカルボン酸、ブタンテ1〜ラ
カルボン酸、ピロメリット酸、エチレンジアミン四酢酸
等の4価のカルボン酸、アクリル酸重合体、アクリル酸
共重合体、メタクリル酸重合体、メタクリル酸共重合体
、アクリル酸やメタクリル酸エステルの重合体や共重合
体の部分ケン化物等が有用であり、それらの部分エステ
ル化物等も例示される。
Examples of carboxylic acids include acetic acid, propionic acid, butyric acid, caproic acid, caprylic acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, benzoic acid, etc.
divalent carboxylic acids, oxalic acid, malonic acid, succinic acid, adipic acid, divalent carboxylic acids such as phthalic acid, hemimelitic acid,
Trivalent carboxylic acids such as trimellitic acid, butante-1-la carboxylic acid, pyromellitic acid, tetravalent carboxylic acids such as ethylenediaminetetraacetic acid, acrylic acid polymers, acrylic acid copolymers, methacrylic acid polymers, methacrylic acid Copolymers, polymers of acrylic acid and methacrylic acid esters, partially saponified products of copolymers, etc. are useful, and partially esterified products thereof are also exemplified.

オキシ酸としては、グリコール酸、乳酸、リンゴ酸、酒
石酸、クエン酸、グルコン酸、オキシ安息香酸、サリチ
ル酸等が挙げられる。
Examples of the oxyacid include glycolic acid, lactic acid, malic acid, tartaric acid, citric acid, gluconic acid, oxybenzoic acid, salicylic acid, and the like.

本発明に係る処理剤は、例えば1級、2級若しくは3級
のアミンとカルボン酸若しくはオキシ酸との通常の中和
反応により容易にI昇ることがてきる。具体的には、ア
ミン中に、液状の酸の場合にはそのまま投入し、固体の
酸の場合には予め水に溶解しておき、所定の当量比にな
る量を入れ、撹拌する。ゲルが生じた場合は50°C以
上で加熱すればよい。
The processing agent according to the present invention can be easily raised to I by, for example, a normal neutralization reaction between a primary, secondary, or tertiary amine and a carboxylic acid or oxyacid. Specifically, in the case of a liquid acid, it is poured into the amine as it is, and in the case of a solid acid, it is dissolved in water in advance, and an amount to achieve a predetermined equivalent ratio is added and stirred. If a gel forms, it may be heated at 50°C or higher.

アミンとカルボン酸若しくはオキシ酸の混合比は当量比
で115〜5/1が有効であり、好ましくは1/2〜2
/1である。この範囲外で使用した場合では性能が著る
しく低下し、処理剤の必要量が増大して経済的に不利と
なる。
An effective equivalent mixing ratio of amine and carboxylic acid or oxyacid is 115 to 5/1, preferably 1/2 to 2.
/1. If it is used outside this range, the performance will be significantly reduced and the amount of processing agent required will increase, resulting in an economic disadvantage.

本発明に係る化合物は2種以上混合して用いても良く、
他の化合物、例えば高扱アルコールのアルキレンオキシ
トイ」加物、アルキルフェノールのアルキレンオキシド
付加物、エチレンオキシド、プロピレンオキシド等の共
重合物、アルキルアミンオキシド等の非イオン活性剤、
アルキルベタイン、アルキルプロピルベタイン 等の両性活性剤、メタノール、エタノール、プロパツー
ル、ブタノール、2−エチルヘキサノール、オレイルア
ルコール等のアルコール類、メチルセロソルブ、エチル
セロソルブ、ブチルセロソルブ、フェニルセロソルブ等
の溶剤を配合することができる。しかし、これらの化合
物はいずれも廃水のCODを上昇させるので、配合量は
処理剤の流動性を保持するために必要な最少足にするべ
きでおる。
The compounds according to the present invention may be used in combination of two or more kinds,
Other compounds, such as alkylene oxide adducts of alcohols, alkylene oxide adducts of alkylphenols, copolymers of ethylene oxide, propylene oxide, etc., nonionic surfactants such as alkylamine oxides,
Containing amphoteric active agents such as alkyl betaine and alkyl propyl betaine, alcohols such as methanol, ethanol, propatool, butanol, 2-ethylhexanol, and oleyl alcohol, and solvents such as methyl cellosolve, ethyl cellosolve, butyl cellosolve, and phenyl cellosolve. Can be done. However, since all of these compounds increase the COD of wastewater, the amount added should be the minimum necessary to maintain the fluidity of the treatment agent.

本発明に係る廃水処理剤は、好ましくは液状で使用され
、その添加量は廃水により異なるが、通常は廃水に対し
て100〜11000ppで充分である。
The wastewater treatment agent according to the present invention is preferably used in liquid form, and the amount added varies depending on the wastewater, but usually 100 to 11,000 ppm to the wastewater is sufficient.

本発明に係る処理剤の使用1)Hは9以下が望ましく、
通常は塩酸、硫酸等の鉱酸により調整する。
Use of the processing agent according to the present invention 1) H is preferably 9 or less,
It is usually adjusted with mineral acids such as hydrochloric acid and sulfuric acid.

この範囲外では油水分離能か大幅に減少する。Outside this range, the oil/water separation ability is significantly reduced.

推奨される使用方法は、常温にて当該化合物を添力nし
、かきまビ、水中に分散している油分を浮上させ、油分
をスキマー等にて除去づ−るか、下層に水をいれ、油分
をオーバーフローさせて回収する。又、油分の浮上を速
くするために、塩化カルシウムや塩化マグネシウム等の
無機塩を添加したり、50〜70°Cに加熱することも
有効で必る。
The recommended method of use is to add the compound at room temperature, stir it, bring the oil dispersed in the water to the surface, and remove the oil with a skimmer, etc., or add water to the bottom layer. , the oil will overflow and be collected. Furthermore, in order to speed up the floating of oil, it is effective to add an inorganic salt such as calcium chloride or magnesium chloride, or to heat it to 50 to 70°C.

本発明に係る当該化合物は、卓越した油水分離能を有し
、処理物の回収、油の再生も容易であり、切削油廃水、
圧延油廃水、ビルジ水、バラスト水等の各種の廃水、特
に水中油滴型エマルション型廃水に適用できる。
The compound according to the present invention has an excellent oil-water separation ability, and it is easy to recover processed materials and regenerate oil, and it is possible to easily recover cutting oil wastewater,
It can be applied to various types of wastewater such as rolling oil wastewater, bilge water, and ballast water, especially oil-in-water emulsion type wastewater.

U実施例コ 以下に実施例でもって本発明の詳細な説明する。U example The present invention will be explained in detail below with reference to Examples.

実施例1 100mlのビーカーに切削油廃水A(濁度:1、OO
Oppm以上、COD : 10.7001)I)m 
)を1003とり、各種処理剤を500 ppm加え、
ノリラス俸にて軽く撹拌して5時間後の濁度、CODを
測定した。処理剤未添加をブランクとして、1ワられた
結果を表に示す。尚、濁度はカオリン:%温液を標準液
としてそれに相当する透過率より算定し、CODはJI
S  K  ○102に準随して求めた。
Example 1 Cutting oil wastewater A (turbidity: 1, OO
Oppm or more, COD: 10.7001)I)m
) to 1003, add 500 ppm of various processing agents,
The mixture was stirred lightly using a Nori-Ras rod, and the turbidity and COD were measured after 5 hours. The table shows the results of one test using no processing agent as a blank. In addition, turbidity is calculated from the transmittance corresponding to kaolin:% warm solution as a standard solution, and COD is calculated from JI
It was obtained in accordance with S K ○102.

実施例2 100m1のビーカーに切削油廃水B(濁度:i、oo
oppm以上、COD : 42,500t)Dm )
を1009とり、各種処理剤を500 ppmと塩化カ
ルシウム500 panとを加え、50℃に加温し、ガ
ラス棒にて軽く撹拌して2時間後の濁度、CODを測定
した。処理剤未添加をブランクとして、得られた結果を
表に示す。
Example 2 Cutting oil wastewater B (turbidity: i, oo
oppm or more, COD: 42,500t)Dm)
1009 was added, 500 ppm of various processing agents and 500 pan of calcium chloride were added, heated to 50°C, stirred lightly with a glass rod, and measured for turbidity and COD after 2 hours. The results obtained are shown in the table, with no treatment agent added as a blank.

実施例3 100彪のビーカーに圧延油廃水(濁度:1.000p
prn以上、COD : 12,600t)DI >を
1009とり、各種処理剤を500 ppm加え、50
’Cに加温し、ガラス棒にて軽く撹拌して2時間後の濁
度、CODを測定した。処理剤未添加をブランクとして
、得られた結果を表に示す。
Example 3 Rolling oil wastewater (turbidity: 1.000 p
prn or more, COD: 12,600t) DI>1009, add 500 ppm of various processing agents, 50
The mixture was heated to 'C and stirred lightly with a glass rod, and the turbidity and COD were measured after 2 hours. The results obtained are shown in the table, with no treatment agent added as a blank.

実施例4 100戴のビーカーにビルジ水A(濁度:1、OOOp
pm以上、COD 二1.320pf)m)を100g
とり、各種処理剤を”+ooppm加え、ガラス棒にて
軽く撹拌し、5時間後の濁度、CODを測定した。処理
剤未添加をブランクとして、得られた結果を表に示す。
Example 4 Bilge water A (turbidity: 1, OOOp
pm or more, COD 21.320pf) m) 100g
After adding ``+ooppm'' of various treatment agents, the mixture was lightly stirred with a glass rod, and the turbidity and COD after 5 hours were measured.The results obtained are shown in the table, with no treatment agent added as a blank.

[発明の効果] 本発明に係る処理剤は、少量の添加と撹拌により水中に
分散している油分その他懸濁物を廃水中から効率良く浮
遊分離することができ、無機系凝集剤を含有する処理剤
に比べて生成するスカムの間も115〜1/10となり
処理費用が軽減できる。
[Effect of the invention] The treatment agent according to the present invention can efficiently float and separate oil and other suspended matter dispersed in water by adding a small amount and stirring, and contains an inorganic flocculant. Compared to processing agents, the amount of scum produced is 115 to 1/10, reducing processing costs.

Claims (1)

【特許請求の範囲】 下記の一般式で表わされる塩を主成分とすることを特徴
とする廃水処理剤。 R^1R^2R^3N・X (式中、R^1は炭素数6〜20のアルキル基、アルケ
ニル基、アラルキル基、フェニル基又はシクロアルキル
基であり、R^2及びR^3は水素若しくは炭素数1〜
20のアルキル基、アルケニル基であり、Xはカルボン
酸若しくはオキシ酸を示す。)
[Scope of Claims] A wastewater treatment agent characterized by containing a salt represented by the following general formula as a main component. R^1R^2R^3N・X (In the formula, R^1 is an alkyl group, alkenyl group, aralkyl group, phenyl group, or cycloalkyl group having 6 to 20 carbon atoms, and R^2 and R^3 are hydrogen Or carbon number 1~
20 alkyl or alkenyl groups, and X represents carboxylic acid or oxyacid. )
JP17613485A 1985-08-10 1985-08-10 Waste water treatment agent Granted JPS6238208A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17613485A JPS6238208A (en) 1985-08-10 1985-08-10 Waste water treatment agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17613485A JPS6238208A (en) 1985-08-10 1985-08-10 Waste water treatment agent

Publications (2)

Publication Number Publication Date
JPS6238208A true JPS6238208A (en) 1987-02-19
JPH0225646B2 JPH0225646B2 (en) 1990-06-05

Family

ID=16008252

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17613485A Granted JPS6238208A (en) 1985-08-10 1985-08-10 Waste water treatment agent

Country Status (1)

Country Link
JP (1) JPS6238208A (en)

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4937033A (en) * 1972-08-14 1974-04-06
JPS53138990A (en) * 1977-05-12 1978-12-04 Teijin Ltd Waste water treating method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4937033A (en) * 1972-08-14 1974-04-06
JPS53138990A (en) * 1977-05-12 1978-12-04 Teijin Ltd Waste water treating method

Also Published As

Publication number Publication date
JPH0225646B2 (en) 1990-06-05

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