JPS61149290A - Method for treatment of phenol-containing waste water - Google Patents

Method for treatment of phenol-containing waste water

Info

Publication number
JPS61149290A
JPS61149290A JP26992384A JP26992384A JPS61149290A JP S61149290 A JPS61149290 A JP S61149290A JP 26992384 A JP26992384 A JP 26992384A JP 26992384 A JP26992384 A JP 26992384A JP S61149290 A JPS61149290 A JP S61149290A
Authority
JP
Japan
Prior art keywords
phenol
treatment
waste water
containing waste
nickel
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
Application number
JP26992384A
Other languages
Japanese (ja)
Inventor
Masahiro Kazama
正博 風間
Yasuo Fujimoto
藤本 康男
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.)
NEC Corp
Original Assignee
NEC Corp
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 NEC Corp filed Critical NEC Corp
Priority to JP26992384A priority Critical patent/JPS61149290A/en
Publication of JPS61149290A publication Critical patent/JPS61149290A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To obtain the titled method excellent in practicality, by mounting a process for performing the electrolytic oxidation of phenol-containing waste water, to which nickel salt and sodium chloride were added, in a pH range of 6.5-7.5. CONSTITUTION:In the treatment of phenol-containing waste water, nickel (II) salt and sodium chloride are added to phenol-containing waste water to adjust the pH thereof to 6.5-7.5. Nickel oxide and sodium hypochlorite formed by anodic oxidation reaction due to electrolytic oxidation are reacted and phenol- containing waste water is rapidly subjected to oxidation treatment by the formed NiO2 and nascent oxygen O.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は薬品製造工場、合成樹脂工場、製鉄工場等より
排吐されるフェノール含有排、水の処理方法に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a method for treating phenol-containing waste water and water discharged from drug manufacturing factories, synthetic resin factories, steel factories, etc.

(従来技術とその問題点) 従来よシ薬品製造工場、合成樹脂工場、製鉄工場等より
排出されるフェノール含有排水を処理する方法として、
活性汚泥法、活性炭吸着法、イオン交換樹脂法等が知ら
れており工業的には活性汚伝法が比較的多く採用されて
いる。しかしながら活性汚伝法は多大な設備投資を必要
とすると供に排水中のフェノール濃度、排水の温度等を
厳密に制御しなければ安定な処理を行なうことが難しい
という欠点を有している。また排水中に含まれるフェノ
ールを活性炭、イオン交換樹脂を用いて吸着除去する方
法に関しても一般的に行なわれているが再生コストが高
い等の欠点を有している。
(Prior art and its problems) Conventionally, as a method for treating phenol-containing wastewater discharged from drug manufacturing factories, synthetic resin factories, steel factories, etc.
The activated sludge method, the activated carbon adsorption method, the ion exchange resin method, etc. are known, and the activated sludge method is relatively often adopted industrially. However, the activated fouling method requires a large investment in equipment and has the disadvantage that it is difficult to perform stable treatment unless the concentration of phenol in the waste water, the temperature of the waste water, etc. are strictly controlled. Furthermore, methods for adsorbing and removing phenol contained in wastewater using activated carbon and ion exchange resins are also commonly used, but these methods have drawbacks such as high regeneration costs.

(発明の目的) 本発明は上記諸問題を解決した実用性に優れたフェノー
ル含有排水の処理方法を提供することにある。
(Objective of the Invention) An object of the present invention is to provide a highly practical method for treating phenol-containing wastewater that solves the above-mentioned problems.

(発明の構成) 本発明はフェノール含有排水にニッケル(璽)塩及び塩
化ナトリウムを添加してpH6,5〜7.5の範囲で電
解酸化する工程を備えたことを特徴とするフェノール含
有排水の処理方法である。
(Structure of the Invention) The present invention provides a process for electrolytically oxidizing phenol-containing wastewater by adding nickel salt and sodium chloride to the phenol-containing wastewater in a pH range of 6.5 to 7.5. This is a processing method.

(構成の詳細な説明) 本発明は例えばフェノールを含有する排水の処理に於い
てまず該排水にニッケル(1)塩及び塩化ナトリウムを
添加し陽極酸化反応によシ生成されるニッケル酸化物及
び次亜塩素酸ナトリウムにより起こる次の様な反応を利
用してフェノール含有排水を処理する方法である。
(Detailed explanation of the structure) The present invention, for example, in treating wastewater containing phenol, first adds nickel (1) salt and sodium chloride to the wastewater, and then nickel oxide and the following are produced by an anodic oxidation reaction. This method uses the following reaction caused by sodium chlorite to treat phenol-containing wastewater.

Ni zOs+NacA!0−+2Ni02+NaCA
’   (1)2Niot+NacJO−)Ni xo
s+Nacl+ 20(11,(2)の反応により生成
された4価のニッケル酸化物N1ot及び発生期の酸素
Oは非常に活性がちシンエノール含有排水は速やかに酸
化処理される。
NizOs+NacA! 0-+2Ni02+NaCA
' (1)2Niot+NacJO-)Nixo
The tetravalent nickel oxide N1ot produced by the reaction of s+Nacl+20(11,(2)) and the nascent oxygen O tend to be very active, and synenol-containing wastewater is rapidly oxidized.

しかもこの場合、4価のニッケル酸化物及び次亜塩素酸
ナトリウムは、反応後陽極酸化を受けて再生され再びフ
ェノール含有排水と繰返し反応するととが可能である。
Furthermore, in this case, the tetravalent nickel oxide and sodium hypochlorite can be regenerated through anodic oxidation after the reaction and can be repeatedly reacted with the phenol-containing wastewater.

また(1)、 (2)を含めた全ての反応に適するpH
範囲はpH6,5〜7.5の範囲でありpHが6.5よ
り小さい範囲では陽極酸化によるニッケル酸化物及び次
亜塩素酸ナトリウムの生成が難しくなり、又J)Hが7
,5より大きい範囲では(1)、 (2)の反応速度が
非常に遅くなる。
Also, the pH suitable for all reactions including (1) and (2)
The pH range is from 6.5 to 7.5, and when the pH is lower than 6.5, it becomes difficult to generate nickel oxide and sodium hypochlorite by anodic oxidation, and J) H is 7.5.
, 5, the reaction rates of (1) and (2) become extremely slow.

更に本発明におけるフェノール含有排水の処理を好まし
〈実施するには例えばフェノール濃度を110001)
pに調整したものにニッケル(璽)塩及び塩化ナトリウ
ムを加える場合ニッケル(f)塩の添加量はフェノール
濃度に対して、ニッケル濃度で11000Pp程度で良
い。
Furthermore, the treatment of phenol-containing wastewater in the present invention is preferable (for example, the phenol concentration is 110,001).
When adding nickel (f) salt and sodium chloride to a product adjusted to p, the amount of nickel (f) salt to be added may be about 11,000 Pp in terms of nickel concentration relative to the phenol concentration.

また塩化ナトリウムの添加量はフェノール濃KK対して
塩化ナトリウム濃度で2000ppm程度で良い。
Further, the amount of sodium chloride added may be about 2000 ppm in terms of sodium chloride concentration relative to phenol-concentrated KK.

この様にしてニッケル(1)塩及び塩化ナトリウムが加
えられたフェノール含有排水は電解酸化されるがこの場
合陽極電位は酸素発生が起こらない範囲で出来るだけ高
くするのが好ましくこのためには酸素過電圧の高い電極
例えば二酸化鉛電極等を用いるのが好ましい。
In this way, phenol-containing wastewater to which nickel (1) salt and sodium chloride have been added is electrolytically oxidized, but in this case it is preferable to make the anode potential as high as possible without causing oxygen generation. It is preferable to use an electrode with a high resistance, such as a lead dioxide electrode.

本発明の方法は従来多く用いられてきた活性汚泥法、活
性炭吸着法、イオン交換樹脂法等とは異なシンエノール
含有排水の処理に対して有利に適用されその排水中のフ
ェノール成分を著しく減少させることが出来る。
The method of the present invention is advantageously applied to the treatment of synenol-containing wastewater, which is different from the conventionally widely used activated sludge method, activated carbon adsorption method, ion exchange resin method, etc., and can significantly reduce the phenol component in the wastewater. I can do it.

次に本発明を実施例により更忙詳細た説明する。Next, the present invention will be explained in more detail with reference to examples.

(実施例) 電解セルとして陽極1枚と陰極1枚並びに撹拌□子1個
を備えた5 00mlビーカーを用いた。
(Example) A 500 ml beaker equipped with one anode, one cathode, and one stirring bar was used as an electrolytic cell.

この場合陽極と陰極の極間距離全10胴にとった。In this case, the distance between the anode and cathode was set to a total of 10 cylinders.

尚陽極には過酸化鉛陰極にはステンレスを用Aた。Stainless steel was used for the anode and lead peroxide cathode.

次にモデル排水として11000Ppのフェノール水溶
液を用いこの水溶液に硫酸ニッケルをニッケル(り濃度
で11000p1)また塩化ナトリウムを塩化ナトリウ
ム濃度で2000pI)mになるi’e添加し更に水酸
化ナトリウムでpHを7.0に調整し撹拌をしなから4
A/di’  の電流密度で電解処理を行なった。その
結果を処理例1.とじて第1図に示す。
Next, using a phenol aqueous solution of 11,000 Pp as a model wastewater, add nickel sulfate (nickel concentration: 11,000 p1) and sodium chloride (concentration: 2,000 pI) to this aqueous solution, and then adjust the pH to 7 with sodium hydroxide. Adjust to .0 and stir 4
Electrolytic treatment was performed at a current density of A/di'. The results are processed in Example 1. It is shown in Figure 1.

(比較例) 次に処理例1と比較するために処理例2〜5を行なった
。その結果をそれぞれ処理例2、処理例3、処理例4、
処理例5として第1図に示す。
(Comparative Example) Next, Processing Examples 2 to 5 were conducted for comparison with Processing Example 1. The results are Processing Example 2, Processing Example 3, Processing Example 4,
Processing example 5 is shown in FIG.

この場合処理例2では1oooppmのフェノール水溶
液に硫酸ニッケル(1)濃度でto’ooppmまた塩
化ナトリウムを塩化ナトリウム濃度で2000ppmに
なる量を添加し更に水酸化ナトリウムでpHを50に調
整し撹拌しなから4A/dm’  の電流密度で電解処
理を行なった二 処理例3では11000pI)のフェノール水溶液に硫
酸ニッケルをニッケル(夏)濃度で1100OT)I)
 iた塩化ナトリウムを塩化ナトリウム濃度で2000
pI)mになる量を添加し更に水酸化ナトリウムでpH
を9.0に調整し撹拌をしなから4A/d−の電流密度
で電解処理を行なった。
In this case, in Treatment Example 2, add to'ooppm of nickel sulfate (1) to a phenol aqueous solution of 100ppm and add sodium chloride in an amount to give a sodium chloride concentration of 2000ppm, adjust the pH to 50 with sodium hydroxide, and stir. In the second treatment example 3, in which electrolytic treatment was performed at a current density of 4 A/dm' from
The sodium chloride concentration is 2000
Add the amount to give pI)m and further adjust the pH with sodium hydroxide.
was adjusted to 9.0 and electrolytic treatment was performed at a current density of 4 A/d- while stirring.

処理例4ではtoooppmのフェノール水溶液ニ塩化
ナトリウムを塩化ナトリウム濃度で2000pI)mに
なる量を加え更に水酸化ナトリウムでpHを7.0に調
整し撹拌をしなから4A/d77f′の電流密度で電解
処理(硫酸ニッケルを添加せず)を行なった。
In treatment example 4, too ppm of an aqueous phenol solution of sodium dichloride was added in an amount to give a sodium chloride concentration of 2000 pI)m, and the pH was adjusted to 7.0 with sodium hydroxide. After stirring, the mixture was heated at a current density of 4 A/d77f'. Electrolytic treatment (without adding nickel sulfate) was performed.

処理例5では11000ppのフェノール水溶液に硫酸
ニッケルをニッケル(璽)濃度でxoooppmになる
量を加え更に水酸化す) IJウムでI)H’に7.O
K調整し撹拌をしなから4A/d−の電流密度で電解処
理(塩化ナトリウムを添加せず)を行なった。
In treatment example 5, nickel sulfate was added to a 11,000 ppm phenol aqueous solution in an amount to give a nickel concentration of xoooppm, and further hydroxylated. O
After adjusting K and stirring, electrolytic treatment was carried out at a current density of 4 A/d- (without adding sodium chloride).

第1図より明らかな様に処理例2においては電解処理開
始よ90.5時間で22%の処理率3時間で80チの処
理率であった。また処理例3においては電解処理開始よ
り0.5時間で18%の処理率、3時間で60%の処理
率であった。更に処理例4゜5においては電解処理開始
より0.5時間で5096の処理率3時間で90%の処
理率であった。
As is clear from FIG. 1, in Treatment Example 2, the treatment rate was 22% at 90.5 hours from the start of the electrolytic treatment, and the treatment rate was 80 cm at 3 hours. Further, in Treatment Example 3, the treatment rate was 18% in 0.5 hours from the start of electrolytic treatment, and 60% in 3 hours. Furthermore, in treatment example 4.5, the treatment rate of 5096 was 90% in 3 hours at 0.5 hours from the start of the electrolytic treatment.

それに対して本発明の処理方法で処理した場合、電解処
理開始よ90.5時間で100チの処理率が得られた〇 尚、実施例においては110001)p のフェノール
水溶液を用すたが5000 pf)mの7エノール水溶
L  1ooooppmのフェノール水溶液、いづれの
場合でも本発明の大きな効果を得ることが出来た。
On the other hand, when the treatment method of the present invention was used, a treatment rate of 100 g was obtained in 90.5 hours from the start of the electrolytic treatment. The great effects of the present invention could be obtained in both cases of 7 enol aqueous solution L of pf)m and phenol aqueous solution of 100 ppm.

(発明の効果) 以上の様に本発明の処理方法でフェノール含有排水を処
理すれば該フェノール含有排水を短時間でしかも高処理
率で処理することが可能である。
(Effects of the Invention) As described above, by treating phenol-containing wastewater with the treatment method of the present invention, it is possible to treat the phenol-containing wastewater in a short time and at a high treatment rate.

また電解処理の最適J)Hが6.5〜7.5の範囲であ
るため後処理用の中和剤の量もわずかで済む他操業上の
危険性、処理装置の腐蝕の問題も少ない等の工業上の大
きな利点がある。
In addition, since the optimum J)H for electrolytic treatment is in the range of 6.5 to 7.5, only a small amount of neutralizing agent is needed for post-treatment, and there are fewer operational risks and corrosion problems of treatment equipment. It has great industrial advantages.

また本発明の方法は季節の影響を受けない他再生作業等
の必要性もなくメンテナンスが著しく容易であるという
効果もある。
Further, the method of the present invention has the advantage that it is not affected by the seasons, and there is no need for regeneration work, etc., and maintenance is extremely easy.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はフェノールの処理率と処理時間との関係を示す
グラフである。
FIG. 1 is a graph showing the relationship between phenol treatment rate and treatment time.

Claims (1)

【特許請求の範囲】[Claims] フェノール含有排水にニッケル(II)塩及び塩化ナトリ
ウムを添加してpHを6.5から7.5の範囲で電解酸
化する工程を備えたことを特徴とするフェノール含有排
水の処理方法。
A method for treating phenol-containing wastewater, comprising the step of adding nickel (II) salt and sodium chloride to the phenol-containing wastewater and electrolytically oxidizing the mixture to a pH in the range of 6.5 to 7.5.
JP26992384A 1984-12-21 1984-12-21 Method for treatment of phenol-containing waste water Pending JPS61149290A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP26992384A JPS61149290A (en) 1984-12-21 1984-12-21 Method for treatment of phenol-containing waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP26992384A JPS61149290A (en) 1984-12-21 1984-12-21 Method for treatment of phenol-containing waste water

Publications (1)

Publication Number Publication Date
JPS61149290A true JPS61149290A (en) 1986-07-07

Family

ID=17479085

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26992384A Pending JPS61149290A (en) 1984-12-21 1984-12-21 Method for treatment of phenol-containing waste water

Country Status (1)

Country Link
JP (1) JPS61149290A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003502154A (en) * 1999-06-18 2003-01-21 バイエル アクチェンゲゼルシャフト How to decompose organic compounds in water
KR100401995B1 (en) * 1998-12-23 2003-12-18 주식회사 포스코 A METHOD FOR PRODUCING HIGH-PURITY NiO BY USING WASTE Ni ANODE

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100401995B1 (en) * 1998-12-23 2003-12-18 주식회사 포스코 A METHOD FOR PRODUCING HIGH-PURITY NiO BY USING WASTE Ni ANODE
JP2003502154A (en) * 1999-06-18 2003-01-21 バイエル アクチェンゲゼルシャフト How to decompose organic compounds in water
JP4641691B2 (en) * 1999-06-18 2011-03-02 バイエル アクチェンゲゼルシャフト Method for decomposing organic compounds in water

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