JPS59169593A - Waste water disposal - Google Patents
Waste water disposalInfo
- Publication number
- JPS59169593A JPS59169593A JP4222283A JP4222283A JPS59169593A JP S59169593 A JPS59169593 A JP S59169593A JP 4222283 A JP4222283 A JP 4222283A JP 4222283 A JP4222283 A JP 4222283A JP S59169593 A JPS59169593 A JP S59169593A
- Authority
- JP
- Japan
- Prior art keywords
- water
- foam
- waste water
- flocks
- tank
- 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.)
- Pending
Links
- 239000002351 wastewater Substances 0.000 title claims abstract description 21
- 230000002378 acidificating effect Effects 0.000 claims abstract description 10
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 9
- 229910017053 inorganic salt Inorganic materials 0.000 claims abstract description 9
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 8
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 6
- 239000002131 composite material Substances 0.000 claims abstract description 6
- 229910052742 iron Inorganic materials 0.000 claims abstract description 6
- 239000006260 foam Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 159000000003 magnesium salts Chemical class 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 25
- 239000012190 activator Substances 0.000 abstract description 24
- 238000006243 chemical reaction Methods 0.000 abstract description 13
- 239000010802 sludge Substances 0.000 abstract description 10
- 229910052749 magnesium Inorganic materials 0.000 abstract description 4
- 239000002480 mineral oil Substances 0.000 abstract description 3
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 244000144992 flock Species 0.000 abstract 4
- 238000002347 injection Methods 0.000 abstract 1
- 239000007924 injection Substances 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 description 19
- 238000000926 separation method Methods 0.000 description 11
- 150000001450 anions Chemical class 0.000 description 5
- 238000004065 wastewater treatment Methods 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 230000015271 coagulation Effects 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 159000000014 iron salts Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 235000020681 well water Nutrition 0.000 description 1
- 239000002349 well water Substances 0.000 description 1
Landscapes
- Physical Water Treatments (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は洗車等によって生じた排水の処理方法に関する
ものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for treating waste water generated from car washing and the like.
一般に洗車排水処理装置は、浮遊物質、ワックス及び鉱
油の処理を目的にしたものであり、洗車排水を放流する
場合、従来の処理装置でも十分に対処できるが、洗車排
水を再使用するため、従来の処理装置で水の回収at高
めると、未処理物質が徐々に蓄積されて濃度障害を発生
させ、満足な洗車ができなくなる。In general, car wash wastewater treatment equipment is designed to treat suspended solids, wax, and mineral oil.When discharging car wash wastewater, conventional treatment equipment can adequately handle the problem, but in order to reuse car wash wastewater, conventional If water recovery is increased in a treatment device, untreated substances will gradually accumulate and cause concentration disturbances, making it impossible to wash cars satisfactorily.
又、従来の処理装置は、洗車排水の高汚濁物質である陰
イオン性界面活性剤(以下アニオン活性剤と略称lる)
の処理性能が非常に低く、アニオン活性剤を数PPMま
でに処理しないと、洗車のリンス工程(水洗)で発泡し
たり、又、ワックス液を白濁させて、ワックスの乗りを
非常に悪くするなどの障害を生ずる。In addition, conventional treatment equipment is capable of treating anionic surfactants (hereinafter abbreviated as anionic surfactants), which are highly polluting substances in car wash wastewater.
The treatment performance is very low, and if the anionic activator is not treated to a few PPM, it may foam during the rinsing process (washing with water) of a car wash, or the wax liquid may become cloudy, making it very difficult to apply the wax. This will cause problems.
現在、洗車排水処理装置として使用されているものには
次のものがある。Currently, the following types of car wash wastewater treatment equipment are used:
(1) 油吸着処理装置
浮遊物質及び油類は処理できるが、アニオン活性剤は全
く処理できない0
(2)凝集沈澱装置
アニオン活性剤の除去率は40〜60%である0
(3) アルミニウム電解処理装置
性能はい)と同じであるが、凝集剤が不要である。(1) Oil adsorption treatment equipment can treat suspended solids and oils, but cannot treat anionic activators at all (2) Coagulation sedimentation equipment has an anionic activator removal rate of 40 to 60% (3) Aluminum electrolysis Treatment equipment performance is the same as (Yes), but no flocculant is required.
(4) 活性炭吸着装置
アニオン活性剤の除去率は90%以上であるが、処理コ
ストが非常に烏い欠点がある。(4) Activated carbon adsorption device Although the removal rate of the anionic activator is 90% or more, it has the disadvantage that the processing cost is extremely high.
本発明の目的は改良された排水処理方法を得るにある。The object of the invention is to obtain an improved method for treating wastewater.
本発明の排水処理方法は、陰イオン性界面活性剤を含有
する排水を酸性状態にて、アルミニウム、鉄、カルシウ
ム及びマグネシウム塩等の無機塩と混合し、無機塩と陰
イオン性界面活性剤との複合物を生成させ、この複合物
を泡沫分離せしめることを特徴とする。In the wastewater treatment method of the present invention, wastewater containing an anionic surfactant is mixed with inorganic salts such as aluminum, iron, calcium, and magnesium salts in an acidic state, and the inorganic salt and anionic surfactant are combined. The method is characterized in that a composite is produced and this composite is separated into foam.
以下図面によって本発明排水処理方法の実施例全説明す
る。Hereinafter, all embodiments of the wastewater treatment method of the present invention will be explained with reference to the drawings.
本発明においてはアニオン活性剤を含有する排水lを反
応槽2内でアルミニウム塩及び鉄塩等の無機塩3と混合
する。無機塩3は加水分解によシ塩酸又は硫酸を発生し
て反応槽2内のPHを弱酸性にし、同時に反応槽2内の
アニオン活性剤と反応してフロラクラ性成する。このフ
ロック生成のときに、浮遊物質、ワックス及び鉱油も凝
集されフロック化される。In the present invention, wastewater l containing an anion activator is mixed in a reaction tank 2 with inorganic salts 3 such as aluminum salts and iron salts. The inorganic salt 3 generates hydrochloric acid or sulfuric acid through hydrolysis to make the pH in the reaction tank 2 weakly acidic, and at the same time reacts with the anion activator in the reaction tank 2 to form a floracura property. During this floc formation, suspended solids, wax and mineral oil are also flocculated and flocculated.
反応槽2からの排水は更に泡沫処理槽4に導入し、フロ
ック含有水を発泡させ未反応のアニオン活性剤で発泡生
成した泡沫にフロックを付着せしめ処理水5として排出
せしめる。The waste water from the reaction tank 2 is further introduced into a foam treatment tank 4, where the floc-containing water is foamed, flocs are attached to the foam generated by foaming with the unreacted anion activator, and the resultant water is discharged as treated water 5.
尚、この泡沫処理槽4ではその内部に散気板又は管6を
配置し、これに空気7を吹き込むようにする。フロック
全多量に付着した泡沫は垂れ下がる間に破泡し、フロッ
クは泡沫水8と共にスラッジ槽9内に溜るようになる。In this foam treatment tank 4, an air diffuser plate or pipe 6 is arranged inside, and air 7 is blown into it. The foam adhering to a large amount of the flocs breaks down while hanging down, and the flocs accumulate in the sludge tank 9 together with the foam water 8.
スラッジ10+″t、疎水性のため泡沫水8上に浮いて
堆積するようになる。The sludge 10+″t floats on the foamy water 8 due to its hydrophobic nature.
本発明においては弱酸性でのアニオン活性剤処理全採用
しているが、アニオン活性剤の代表であるABS(アル
キルベンゼンスルホン酸ソーダ)と硫酸アルミニウムと
”5 P H4,0〜9.0の間で反応させり場合のア
ニオン活性剤の除去率を第1表に示す。In the present invention, a weakly acidic anionic activator treatment is adopted, but ABS (sodium alkylbenzene sulfonate), which is a typical anionic activator, and aluminum sulfate are treated with a 5 PH between 4.0 and 9.0. Table 1 shows the removal rate of the anionic activator in the case of reaction.
第1表
処理剤の無機塩には、アルミニウム、鉄、カルシウム及
びマグネシウムなどがあるが、アニオン活性材の処理性
能、他の汚濁粒子(フック、z、 、 油、 砂)の凝
集性能において、アルミニウム塩がすぐれている。硫酸
アルミニウムの水溶液である液体硫酸パン土(LAS)
は、排水に加えると自己の加水分解により硫酸を生じる
ので、排水に酸を加えなくても弱酸性になる。The inorganic salts used in Table 1 treatment agents include aluminum, iron, calcium, and magnesium. The salt is excellent. Liquid earth sulfate (LAS) is an aqueous solution of aluminum sulfate.
When added to wastewater, it produces sulfuric acid through its own hydrolysis, so it becomes weakly acidic even without adding acid to the wastewater.
陰イオン活性剤のナトリウムやアミンは無機塩のアルミ
ニウム、鉄、カルシウム及びマグネシウムと置換される
ことによシ、下式のようにアニオン活性剤−無機塩の複
合体フロックを生成する。Anionic activator sodium and amine are replaced with inorganic salts of aluminum, iron, calcium, and magnesium, thereby producing an anionic activator-inorganic salt composite floc as shown in the following formula.
6C12H25−■−8O3Na + A4 (So、
)3→2 (C+2 H2s−CりSOs )3 A
t + 3Na2804第1表よりアニオン活性剤の種
類は多いが、PH4,5〜5.5でフロック化した時の
除去率が高いことが判る。アニオン活性剤フロックの溶
解度は弱酸性で最小であって、PHが高くなるにつれて
溶解度も高くなる。逆に、PHが4以下になると、アニ
オン活性剤フロックが生QLにく 〈 ンと る 。6C12H25-■-8O3Na + A4 (So,
)3→2 (C+2 H2s-CriSOs)3 A
t+3Na2804 Table 1 shows that although there are many types of anion activators, the removal rate is high when flocculated at pH 4.5 to 5.5. The solubility of anionic activator flocs is minimal at weakly acidic conditions and increases as the pH increases. Conversely, when the pH becomes 4 or less, the anionic activator floc is concentrated in the raw QL.
尚、従来泡沫分離は洗剤等の溶解物質の除去が目的であ
ったが、本発明では反応槽2で生成した多量の70ツク
を短時間に泡沫分離するものである。In the past, the purpose of foam separation was to remove dissolved substances such as detergents, but in the present invention, a large amount of 70 pieces generated in the reaction tank 2 is separated into foam in a short time.
一般にフロックを泡沫分離して非常に清澄な処理水を得
ることは困難で、泡沫によるフロック等の粒子の分pJ
11は非常KM雑な界面現象を応用しており、フロック
がより疎水性(ぬれにくい)であることが1要である。Generally, it is difficult to obtain extremely clear treated water by separating flocs into foam, and the amount of particles such as flocs caused by foam is pJ.
No. 11 applies a very KM rough interface phenomenon, and one important point is that the floc is more hydrophobic (hard to wet).
アニオン活性剤フロックの疎水性はPI(により変化し
、生成したアニオン活性剤フロック’kPH’に変えて
泡沫処理するとアニオン活性剤の除去率が高い弱酸性で
は95%以上のフロック除去率となり、中性、弱アルカ
リ性では50%以下のフロック除去率となる。The hydrophobicity of the anionic activator floc changes with PI (PI), and when the generated anionic activator floc 'kPH' is treated with foam, the removal rate of the anionic activator is high.In weak acidity, the floc removal rate is over 95%, and in the case of medium Under strong and weakly alkaline conditions, the floc removal rate is less than 50%.
70ツクの泡沫分MはPHの他にフロック粒子の大きさ
が重要であり、フロックが十分に凝集した場合は10分
程度の滞留時間で完全に)ロックが泡沫分離できるが、
外見上、白濁したような微細フロックは泡沫分離に非常
に長時間(30分以上)必要である。又、アニオン活性
剤と無機塩との反応促進のために反応槽内は高効率であ
るプロペラ11等によシ攪拌することが必要になる。In addition to the pH, the size of the floc particles is important for the foam content M of 70 tsuku.If the flocs are sufficiently agglomerated, the foam can be completely separated from the flocs in a residence time of about 10 minutes.
Fine flocs that appear cloudy require a very long time (more than 30 minutes) to separate the foam. Further, in order to promote the reaction between the anion activator and the inorganic salt, it is necessary to stir the inside of the reaction tank using a highly efficient propeller 11 or the like.
アニオン活性剤フロックの分離は弱酸性で粒径の大きい
根分離しやすく、沈澱槽の17.〜1/の大きさで、沈
澱処理では得られない清澄な処理水が得られる。空気流
量と処理流量との比(空/液)は′IA〜15/1が最
適であり、空気流量が少なすぎると、泡は泡沫分離槽か
ら排出できず、又、逆に多すぎると泡沫水の量が多くな
って水の回収率が低くなり、空/液が′7/1〜10/
1では泡沫水として損失する割合は3チ以下となる。Separation of anionic activator flocs is weakly acidic and roots with large particle sizes are easily separated, and 17. With a size of ~1/2, clear treated water that cannot be obtained by precipitation treatment can be obtained. The optimal ratio of air flow rate to processing flow rate (empty/liquid) is 'IA ~ 15/1; if the air flow rate is too low, foam cannot be discharged from the foam separation tank, and conversely, if it is too high, foam The amount of water increases, the water recovery rate decreases, and the empty/liquid ratio is from 7/1 to 10/10.
1, the percentage lost as foam water is less than 3 inches.
本発明方法による泡沫分離の泡沫は非常に多量のフロッ
クを付着し、このため泡の発泡が適当に抑制され、しか
も破泡性であシ、通常の泡沫分離に必要な破泡装置や消
泡剤は必要とせず、泡沫の殆どは泡沫分離槽を垂れ下が
る間に破泡し、泡沫がスラッジ槽から溢れることはない
。The foam separated by the method of the present invention has a very large amount of flocs attached to it, so that the foaming of the foam is appropriately suppressed, and it is not foam-breaking. No agent is required, most of the foam breaks while hanging down through the foam separation tank, and no foam overflows from the sludge tank.
又、泡沫分離にはフロック及び未反応のアニオン活性剤
の分離の他に酸の分離がある。In addition to the separation of flocs and unreacted anionic activator, foam separation includes separation of acid.
この酸は無機塩の加水分解で生じたものであるが、泡沫
分離である程度は除去でき、泡沫処理水のPHは反応槽
のPHより0.6〜1.θ程度高くなる。このため、処
理水を再利用する場合、泡沫処理水にアルカ’J’fz
加える必要はない。This acid is generated by hydrolysis of inorganic salts, but it can be removed to some extent by foam separation, and the pH of the foam-treated water is 0.6 to 1. It becomes higher by about θ. Therefore, when reusing treated water, Alka'J'fz is added to the foamed treated water.
No need to add.
再オU用を行うと、水道水(井戸水)中のアルカリ成分
が反応槽で消費されるが、洗車用洗剤には助剤(りん酸
塩、ケイ酸ソーダ等)としてのアルカリ成分があるので
、本発明ではアルカリを加えなくても再利用水のPHが
強酸性になることはない。7反応槽のPHvf−5付近
になるように無機塩を添加していれば、処理水は常にP
H5,6〜6に保つことができるう
本発明方法によって排出したフロックは非常に疎水性で
あるので、泡沫水に浮いて堆積される。スラッジは低含
水率であるから掻き出すことができ、しかも自然乾燥で
きるので非常に処理しやすいオリ点がある。When re-washing, the alkaline components in the tap water (well water) are consumed in the reaction tank, but car wash detergents contain alkaline components as auxiliaries (phosphates, sodium silicate, etc.). In the present invention, the pH of the reused water does not become strongly acidic even without adding alkali. 7 If inorganic salts are added so that the PHvf of the reaction tank is around -5, the treated water will always have a P
The flocs discharged by the method of the present invention, which can be maintained at H5, 6 to 6, are very hydrophobic and are therefore deposited floating in foamy water. Since sludge has a low moisture content, it can be scraped out and dried naturally, so it has a very easy-to-process sludge point.
本発明方法は他の分野にも適用できる。The method of the invention can also be applied to other fields.
例えば陰イオン活性剤を含む排水ならば洗車排水以外に
も問題なく適用できる。又、凝集沈澱及び凝集加圧浮上
処理に適する排水の場合、アルミニウム凝集剤と安価な
アニオン活性剤を併用すれば、排水にアニオン活性剤が
なくても本発明を適用できる。本発明を適用すれば、フ
ロック分離槽がA以下になシ、又、フロック醐出も泡沫
分離であるので、分離槽内に蓄積するスラッジを排出す
る必要がない。特に有利なことは、処理水の透明度が非
常に高いので清澄濾過が必要でない場合が多いことであ
る。For example, if the wastewater contains an anionic activator, it can be applied to other than car wash wastewater without any problem. Further, in the case of wastewater suitable for coagulation sedimentation and coagulation pressure flotation treatment, the present invention can be applied even if the wastewater does not contain an anionic activator by using an aluminum flocculant and an inexpensive anionic activator in combination. If the present invention is applied, the floc separation tank will not be smaller than A, and since the floc removal is also foam separation, there is no need to discharge the sludge accumulated in the separation tank. A particular advantage is that the clarity of the treated water is so high that clarifying filtration is often not necessary.
本発明による処理性能を第2表に示す。Table 2 shows the processing performance according to the present invention.
図は本発明排水処理方法を示すZローシートである。
1・・・排水、2・・・反応槽、3・・・無機塩、4・
・・泡沫処理槽、5・・・処理水、6・・・散気板又は
管、7・・・空気、8・・・泡沫水、9・・・スラッジ
槽、10・・・スラッジ、11・・・プロペラ。The figure is a Z-row sheet showing the wastewater treatment method of the present invention. 1... Drainage, 2... Reaction tank, 3... Inorganic salt, 4...
... Foam treatment tank, 5... Treated water, 6... Diffuser plate or pipe, 7... Air, 8... Foam water, 9... Sludge tank, 10... Sludge, 11 ···propeller.
Claims (1)
アルミニウム、鉄、カルシウム及びマグネシウム塩等の
無機塩と混合し、無機塩と陰イオン性界面活性剤との複
合物を生成させ、この複合物を泡沫分離せしめることを
特徴とする排水処理方法。Wastewater containing anionic surfactants is treated in acidic conditions.
A method for treating wastewater, which comprises mixing with inorganic salts such as aluminum, iron, calcium, and magnesium salts to form a composite of the inorganic salt and anionic surfactant, and separating this composite into foam.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4222283A JPS59169593A (en) | 1983-03-16 | 1983-03-16 | Waste water disposal |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4222283A JPS59169593A (en) | 1983-03-16 | 1983-03-16 | Waste water disposal |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS59169593A true JPS59169593A (en) | 1984-09-25 |
Family
ID=12630006
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4222283A Pending JPS59169593A (en) | 1983-03-16 | 1983-03-16 | Waste water disposal |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59169593A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008238030A (en) * | 2007-03-27 | 2008-10-09 | Kurita Water Ind Ltd | Aggregation method |
-
1983
- 1983-03-16 JP JP4222283A patent/JPS59169593A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008238030A (en) * | 2007-03-27 | 2008-10-09 | Kurita Water Ind Ltd | Aggregation method |
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