JPH06182362A - Treatment of dyeing waste water - Google Patents
Treatment of dyeing waste waterInfo
- Publication number
- JPH06182362A JPH06182362A JP4361819A JP36181992A JPH06182362A JP H06182362 A JPH06182362 A JP H06182362A JP 4361819 A JP4361819 A JP 4361819A JP 36181992 A JP36181992 A JP 36181992A JP H06182362 A JPH06182362 A JP H06182362A
- Authority
- JP
- Japan
- Prior art keywords
- tank
- oxidation
- coagulant
- dye
- cod
- 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
Landscapes
- Treatment Of Water By Oxidation Or Reduction (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Removal Of Specific Substances (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、反応性染料等の難脱色
性染料を含有する染色廃水の処理法に関し、更に詳しく
は、フェントン試薬法を用いた染色廃水処理法の改良に
関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating dyeing wastewater containing a difficult-to-decolorize dye such as a reactive dye, and more particularly to improvement of a method for treating dyeing wastewater using the Fenton's reagent method.
【0002】[0002]
【従来の技術】周知のように、フェントン試薬法では、
鉄塩系の触媒下で過酸化水素の強力な酸化力により廃水
中の有機物を酸化分解した後、酸化反応液に消石灰等の
凝集剤を添加し、生ずるフロックを固液分離により除去
するものであり、アゾ系、アントラキノン系等の染色廃
水の脱色処理に優れた効果を発揮するものである。As is well known, in the Fenton reagent method,
After oxidizing and decomposing organic matter in wastewater by the strong oxidizing power of hydrogen peroxide under iron salt catalyst, flocculating agent is added by adding coagulant such as slaked lime to the oxidation reaction liquid and solid-liquid separation. Therefore, it exhibits an excellent effect on the decolorization treatment of dyeing wastewater such as azo type and anthraquinone type.
【0003】しかしながら、フタロシアニン系等の反応
性染料を含有する染色廃水の脱色には、その脱色効果を
十分発揮できるものではなかった。また、多量の過酸化
水素、鉄塩、消石灰等の薬品を必要とし、更にそれに伴
い多量の汚泥が発生するといった欠点があり、経済性の
面でも問題があった。However, the decolorizing effect of the dyeing wastewater containing a reactive dye such as a phthalocyanine type dye has not been sufficiently exhibited. In addition, there is a drawback in that a large amount of chemicals such as hydrogen peroxide, iron salt, and slaked lime is required, and further, a large amount of sludge is generated, which is a problem from the economical aspect.
【0004】[0004]
【発明が解決しようとする課題】本発明は、上述のよう
な実状に鑑みて成されたもので、その目的とするところ
は、反応性染料等の脱色されにくい染料を含有する染色
廃水の処理法として脱色効果、COD除去効果に優れ、
併せて経済性をも改善できる新規な廃水処理法を提供す
るものである。SUMMARY OF THE INVENTION The present invention has been made in view of the above situation, and an object thereof is to treat a dyeing wastewater containing a dye that is difficult to be decolorized such as a reactive dye. As a method, it is excellent in decolorizing effect and COD removing effect,
At the same time, it provides a new wastewater treatment method that can improve economic efficiency.
【0005】[0005]
【課題を解決するための手段】しかるに本発明は、染色
廃水を、鉄塩を触媒として過酸化水素でpH≦3で酸化
槽1にて酸化処理し、しかる後、該処理液をpH調整槽
7にてpH=6〜7に調整後、薬品混合槽8にて該処理
液にアルミ系凝集剤、凝結剤を添加し、しかる後、凝集
槽9にて高分子凝集剤を添加して凝集沈澱により固液を
分離除去することに特徴を有する染色廃水処理法に関す
る。According to the present invention, however, the dyeing wastewater is oxidized with hydrogen peroxide using iron salt as a catalyst at a pH ≦ 3 in an oxidation tank 1, and then the treatment liquid is subjected to a pH adjusting tank. After adjusting the pH to 6 to 7 in step 7, an aluminum-based coagulant and a coagulant are added to the treatment liquid in the chemical mixing tank 8, and then a polymer coagulant is added in the coagulating tank 9 to coagulate. The present invention relates to a dyeing wastewater treatment method characterized by separating and removing solid-liquid by precipitation.
【0006】[0006]
【作用】前記構成において染色廃水を、鉄塩を触媒とし
て過酸化水素でpH≦3で酸化処理すると限定したの
は、かかる条件でなければ、酸化処理の有効な反応が起
こらないからである。また、酸化処理した液をpH調整
槽7にてpH=6〜7に調整するのは、前処理として凝
集剤、凝結剤の働きを高めるためであり、もし、このp
H調整槽7のpHがアルカリであれば、凝集剤と反応し
てしまい、フロックを形成することができなくなってし
まうからである。In the above construction, the dyeing wastewater is limited to be oxidized with hydrogen peroxide at pH≤3 using an iron salt as a catalyst because an effective reaction of the oxidation treatment does not occur unless such conditions are met. Further, the reason why the pH of the oxidized liquid is adjusted to 6 to 7 in the pH adjusting tank 7 is to enhance the functions of the coagulant and the coagulant as pretreatment.
This is because if the pH of the H adjusting tank 7 is alkaline, it reacts with the aggregating agent and it becomes impossible to form flocs.
【0007】次に、鉄塩としては、硫酸第一鉄、硫酸第
二鉄、硫酸第二鉄第一鉄等の無水塩、及びそれらの含水
塩が例示できる。また、アルミ系の凝集剤としては、ポ
リ塩化アルミ(PAC)、硫酸バンド等が例示でき、凝
結剤としてはカチオン系のポリアミン樹脂等が例示で
き、高分子凝集剤としては、アニオン系のポリアクリル
アミド等が例示できる。Examples of the iron salt include anhydrous salts of ferrous sulfate, ferric sulfate, ferrous sulfate and ferrous sulfate, and hydrous salts thereof. Examples of the aluminum-based coagulant include polyaluminum chloride (PAC), sulfuric acid band, etc., examples of the coagulant include cationic polyamine resin, and examples of the polymer coagulant include anionic polyacrylamide. Etc. can be illustrated.
【0008】また、前記構成における凝集剤の主な働き
は、フロックを形成させることにあり、これは槽内を撹
拌させながら用いられるが、この時の撹拌速度は速い方
が好ましい。一方、高分子凝集剤の主な働きは、フロッ
クを成長させることにあり、この時の撹拌速度は、凝集
剤の時とは逆に遅い方が好ましい。また、カチオン系の
凝結剤の主な働きは、染料成分中のアニオンと反応する
ことであり、併用した凝集剤や、更には高分子凝集剤の
働きによって、染色廃水を凝集沈澱により固液分離する
ことができる。Further, the main function of the flocculant in the above constitution is to form flocs, which are used while stirring the inside of the tank, and the stirring speed at this time is preferably high. On the other hand, the main action of the polymer flocculant is to grow flocs, and the stirring speed at this time is preferably slower than that of the flocculant. Also, the main function of the cationic coagulant is to react with the anions in the dye component, and the coagulant used in combination and the polymer coagulant function together to separate the dyeing wastewater by solid-liquid separation by coagulation precipitation. can do.
【0009】また、本発明は、染色廃水中に含有する反
応性染料等の難脱色性の染料の脱色に効果を発揮するも
のであるが、これに限定されるものではなく、染色廃水
中に反応性染料等の難脱色性の染料を含有しなくても良
い。Further, the present invention is effective for decolorizing a hardly decolorizing dye such as a reactive dye contained in the dyeing wastewater, but the present invention is not limited to this, and is not limited to the dyeing wastewater. It is not necessary to contain a difficult-to-decolorize dye such as a reactive dye.
【0010】以下、従来法及び本発明を図面に基づき説
明する。図1は、フェントン試薬法による従来の廃水処
理法を表した図である。かかる処理法では、まず染色廃
水を酸化槽1へ送り、鉄塩を触媒として過酸化水素によ
り酸化処理する。この時、酸化槽1のpHは、硫酸等の
無機酸によりpH≦3に調整されており、撹拌プロペラ
5により十分な速度で撹拌されている。次に、凝集槽2
で消石灰等の凝集剤を添加する。この時、凝集槽2のp
Hは、カセイソーダ等のアルカリによりpH=8〜10
に調整されている。次に、沈澱槽3で固液分離された
後、汚泥はポンプ6により投棄し、上澄み液は中和槽4
でpH=7に調整した後放流する。The conventional method and the present invention will be described below with reference to the drawings. FIG. 1 is a diagram showing a conventional wastewater treatment method by the Fenton reagent method. In such a treatment method, first, the dyeing wastewater is sent to the oxidation tank 1 and is oxidized with hydrogen peroxide using an iron salt as a catalyst. At this time, the pH of the oxidation tank 1 is adjusted to pH ≦ 3 by an inorganic acid such as sulfuric acid, and is stirred at a sufficient speed by the stirring propeller 5. Next, flocculation tank 2
Add a flocculant such as slaked lime. At this time, p in the coagulation tank 2
H is pH = 8 to 10 due to alkali such as caustic soda
Has been adjusted to. Next, after solid-liquid separation in the settling tank 3, sludge is discarded by the pump 6, and the supernatant liquid is neutralized in the neutralization tank 4.
After adjusting the pH to 7, the product is discharged.
【0011】図2は、本発明による廃水処理法を表した
図である。本発明によれば、染色廃水をまず酸化槽1
で、フェントン試薬法により酸化処理する。次に、pH
調整槽7で、カセイソーダ等のアルカリによりpH=6
〜7に調整し、薬品混合槽8で、アルミ系凝集剤、凝結
剤を添加する。次に、凝集槽9で高分子凝集剤を添加
し、沈澱槽3で固液分離された後、汚泥はポンプ6によ
り投棄し、上澄み液はpH=7に調整した後放流する。FIG. 2 is a diagram showing a wastewater treatment method according to the present invention. According to the invention, the dyeing wastewater is first treated in the oxidation tank 1
Then, oxidation treatment is performed by the Fenton reagent method. Then pH
In the adjusting tank 7, pH = 6 with alkali such as caustic soda.
Adjust to 7 and add aluminum coagulant and coagulant in the chemical mixing tank 8. Next, a polymer flocculant is added in the flocculation tank 9, and solid-liquid separation is performed in the precipitation tank 3, sludge is discarded by the pump 6, and the supernatant liquid is discharged after adjusting it to pH = 7.
【0012】以下、本発明の実施例及び従来法による比
較例を挙げて説明する。Hereinafter, examples of the present invention and comparative examples by a conventional method will be described.
【実施例1】染料としてヘキスト社製のレマゾールグリ
ーン 6B(Remazol Green 6B)を2
00mg/l含有するフタロシアニン系の染色廃液に対
して、以下の条件で廃水処理を行った。即ち、フェント
ン試薬として過酸化水素400mg/l、硫酸第一鉄7
水塩80mg/lを用い、酸化条件としては、酸化温度
26〜30℃、酸化時間1.0時間、酸化槽のpH=
2.7とした。また、アルミ系凝集剤としてポリ塩化ア
ルミを300mg/l、凝結剤として水溶性ポリアミン
樹脂を50〜300mg/l、高分子凝集剤としてポリ
アクリルアミド(アニオン)を1mg/lとした。以上
のような条件下で次の操作を行った。即ち、酸化槽1で
酸化処理終了後、直ちにpH調整槽7でNaOHによ
り、pH=6.3に調整し、薬品混合槽8でアルミ系凝
集剤、凝結剤を添加した後、凝集槽9で高分子凝集剤を
添加して沈澱槽3で固液を沈澱分離後、かかる上澄み液
について透過率及びCODを測定した。但し、原液の透
過率は0%で、CODは110mg/lである。また、
透過率は、マクベス CE3000W 分光光度計(5
00nm)で測定し、CODは、JIS−K 0102
(100℃における過マンガン酸カリウムによる酸素消
費量)法で測定した。Example 1 As a dye, 2 pieces of Remazol Green 6B manufactured by Hoechst Co. were used.
The phthalocyanine-based dyeing waste liquid containing 00 mg / l was subjected to wastewater treatment under the following conditions. That is, hydrogen peroxide 400 mg / l, ferrous sulfate 7 as Fenton's reagent
Using 80 mg / l of water salt, the oxidation conditions are as follows: oxidation temperature 26 to 30 ° C., oxidation time 1.0 hour, pH of oxidation tank
It was set to 2.7. In addition, polyaluminum chloride was used as an aluminum-based coagulant at 300 mg / l, a water-soluble polyamine resin as a coagulant was 50 to 300 mg / l, and polyacrylamide (anion) as a polymer coagulant was 1 mg / l. The following operation was performed under the above conditions. That is, immediately after the completion of the oxidation treatment in the oxidation tank 1, the pH is adjusted to 6.3 with NaOH in the pH adjustment tank 7, the aluminum-based coagulant and the coagulant are added in the chemical mixing tank 8, and then in the coagulation tank 9. A polymer flocculant was added and the solid-liquid was precipitated and separated in the precipitation tank 3. Then, the transmittance and COD of the supernatant were measured. However, the transmittance of the stock solution is 0% and the COD is 110 mg / l. Also,
The transmittance is based on the Macbeth CE3000W spectrophotometer (5
00 nm) and the COD is JIS-K 0102.
(Oxygen consumption by potassium permanganate at 100 ° C.) method.
【0013】実施例1との比較のために従来法による廃
水処理を以下の条件で行った。For comparison with Example 1, wastewater treatment by the conventional method was carried out under the following conditions.
【比較例1】即ち、染料としてヘキスト社製のレマゾー
ルグリーン 6B(RemazolGreen 6B)
を200mg/l含有するフタロシアニン系の染色廃液
に対して、フェントン試薬として過酸化水素1000m
g/l、硫酸第一鉄7水塩400mg/lを用い、酸化
条件としては、酸化温度30〜35℃、酸化時間2.5
時間、酸化槽のpH=3.0とした。以上のような条件
下で次の操作を行った。即ち、酸化槽1で酸化処理終了
後、直ちに凝集槽2で、NaOHによりpH=10に調
整し、しかる後沈澱槽3で固液を沈澱分離後、かかる上
澄み液について透過率及びCODを実施例1と同様の方
法で測定した。但し、原液の透過率は0%で、CODは
110mg/lである。Comparative Example 1 That is, as a dye, Remazol Green 6B manufactured by Hoechst Co., Ltd.
1000m of hydrogen peroxide as a Fenton's reagent for a phthalocyanine dye waste solution containing 200mg / l of
g / l, ferrous sulfate heptahydrate 400 mg / l, and the oxidation conditions are as follows: oxidation temperature 30 to 35 ° C., oxidation time 2.5.
Time, pH of the oxidation tank was set to 3.0. The following operation was performed under the above conditions. That is, immediately after the completion of the oxidation treatment in the oxidation tank 1, the pH was adjusted to 10 with NaOH in the coagulation tank 2, and after the solid-liquid was precipitated and separated in the precipitation tank 3, the transmittance and COD of the supernatant liquid were measured. The measurement was performed in the same manner as in 1. However, the transmittance of the stock solution is 0% and the COD is 110 mg / l.
【0014】以上のようにして得た実施例1及び比較例
1における透過率及びCODの測定結果は、表1に示す
通りである。The measurement results of transmittance and COD in Example 1 and Comparative Example 1 obtained as described above are as shown in Table 1.
【0015】[0015]
【表1】 [Table 1]
【0016】[0016]
【実施例2】染料としてバイエル社製のレバフィックス
ターコイズブルー E−BA(Levafix Tur
quoise Blue E−BA)を200mg/l
含有するフタロシアニン系の染色廃液に対して、以下の
条件で行った。即ち、フェントン試薬として過酸化水素
400mg/l、硫酸第一鉄7水塩80mg/lを用
い、酸化条件としては、酸化温度26〜30℃、酸化時
間1.0時間、酸化槽のpH=2.7とした。また、ア
ルミ系凝集剤としてポリ塩化アルミを300mg/l、
凝結剤として水溶性ポリアミン樹脂を50〜300mg
/l、高分子凝集剤としてポリアクリルアミド(アニオ
ン)を1mg/lとした。以上のような条件下で実施例
1と同様の操作を行い、上澄み液について透過率及びC
ODを測定した。但し、原液の透過率は0%で、COD
は110mg/lである。Example 2 As a dye, Levafix Turquoise Blue E-BA (Levafix Tur manufactured by Bayer Co., Ltd.)
quiose Blue E-BA) 200 mg / l
The phthalocyanine-based dyeing waste liquid contained was subjected to the following conditions. That is, hydrogen peroxide 400 mg / l and ferrous sulfate heptahydrate 80 mg / l were used as the Fenton's reagent, and the oxidation conditions were as follows: oxidation temperature 26 to 30 ° C., oxidation time 1.0 hour, oxidation tank pH = 2. It was set to 7. Also, 300 mg / l of polyaluminum chloride as an aluminum-based coagulant,
50-300 mg of water-soluble polyamine resin as a coagulant
/ L, and polyacrylamide (anion) as a polymer flocculant was 1 mg / l. The same operation as in Example 1 was carried out under the above conditions, and the transmittance and C
The OD was measured. However, the transmittance of the stock solution is 0%, and COD
Is 110 mg / l.
【0017】実施例2との比較のために従来法による廃
水処理を以下の条件で行った。For comparison with Example 2, wastewater treatment by the conventional method was carried out under the following conditions.
【比較例2】即ち、染料としてバイエル社製のレバフィ
ックスターコイズブルー E−BA(Levafix
Turquoise Blue E−BA)を200m
g/l含有するフタロシアニン系の染色廃液に対して、
フェントン試薬として過酸化水素1000mg/l、硫
酸第一鉄7水塩400mg/lを用い、酸化条件として
は、酸化温度30〜35℃、酸化時間1時間、酸化槽の
pH=3.0とした。以上のような条件下で、比較例1
と同様の操作を行い、上澄み液について透過率及びCO
Dを測定した。但し、原液の透過率は0%で、CODは
110mg/lである。Comparative Example 2 That is, as a dye, Levafix Turquoise Blue E-BA (Levafix) manufactured by Bayer Co., Ltd.
Turquoise Blue E-BA) 200m
For phthalocyanine dye waste liquid containing g / l,
Hydrogen peroxide (1000 mg / l) and ferrous sulfate heptahydrate (400 mg / l) were used as Fenton's reagent, and the oxidation conditions were as follows: oxidation temperature 30 to 35 ° C., oxidation time 1 hour, and oxidation tank pH = 3.0. . Under the conditions as described above, Comparative Example 1
The same operation as above is carried out, and the transmittance and CO
D was measured. However, the transmittance of the stock solution is 0% and the COD is 110 mg / l.
【0018】以上のようにして得た実施例2及び比較例
2における透過率及びCODの測定結果は、表2に示す
通りである。The measurement results of transmittance and COD in Example 2 and Comparative Example 2 obtained as described above are as shown in Table 2.
【0019】[0019]
【表2】 [Table 2]
【0020】[0020]
【実施例3】染料としてサンド社製のドリマレンネービ
ー X−RBL(Drimarene Navy X−
RBL)を200mg/l含有するアゾ系の染色廃液に
対して、以下の条件で行った。即ち、フェントン試薬と
して過酸化水素400mg/l、硫酸第一鉄7水塩80
mg/lを用い、酸化条件としては、酸化温度26〜3
0℃、酸化時間1.0時間、酸化槽のpH=2.7とし
た。また、アルミ系凝集剤としてポリ塩化アルミを30
0mg/l、凝結剤として水溶性ポリアミン樹脂を50
〜300mg/l、高分子凝集剤としてポリアクリルア
ミド(アニオン)を1mg/lとした。以上のような条
件下で、実施例1と同様の操作を行い、上澄み液につい
て透過率及びCODを測定した。但し、原液の透過率は
11%で、CODは96mg/lである。[Example 3] As a dye, Drimalene Navy X-RBL (Drimarene Navy X- manufactured by Sand Co., Ltd.)
RBL) was applied to an azo dyeing waste liquid containing 200 mg / l under the following conditions. That is, hydrogen peroxide 400 mg / l, ferrous sulfate heptahydrate 80 as Fenton's reagent
Using mg / l, the oxidation conditions are oxidation temperature 26 to 3
The temperature was 0 ° C., the oxidation time was 1.0 hour, and the pH of the oxidation tank was 2.7. Moreover, polyaluminum chloride is used as an aluminum-based coagulant.
0 mg / l, 50% water-soluble polyamine resin as a coagulant
˜300 mg / l, and polyacrylamide (anion) as a polymer flocculant was 1 mg / l. Under the above conditions, the same operation as in Example 1 was performed, and the transmittance and COD of the supernatant liquid were measured. However, the transmittance of the stock solution was 11% and the COD was 96 mg / l.
【0021】実施例3との比較のために従来法による廃
水処理を以下の条件で行った。For comparison with Example 3, wastewater treatment by the conventional method was carried out under the following conditions.
【比較例3】即ち、染料としてサンド社製のドリマレン
ネービー X−RBL(Drimarene Navy
X−RBL)を200mg/l含有するアゾ系の染色
廃液に対して、フェントン試薬として過酸化水素800
mg/l、硫酸第一鉄7水塩500mg/lを用い、酸
化条件としては、酸化温度30〜35℃、酸化時間2.
5時間、酸化槽のpH=3.0とした。以上のような条
件下で、比較例1と同様の操作を行い、上澄み液につい
て透過率及びCODを測定した。但し、原液の透過率は
11%で、CODは96mg/lである。[Comparative Example 3] That is, as a dye, Drimalene Navy X-RBL (Drimarene Navy) manufactured by Sand Co.
X-RBL) to 200 mg / l of the azo dye waste solution, hydrogen peroxide 800 as Fenton's reagent
1. mg / l, ferrous sulfate heptahydrate 500 mg / l were used, and the oxidation conditions were an oxidation temperature of 30 to 35 ° C. and an oxidation time of 2.
The pH of the oxidation tank was set to 3.0 for 5 hours. Under the above conditions, the same operation as in Comparative Example 1 was performed, and the transmittance and COD of the supernatant liquid were measured. However, the transmittance of the stock solution was 11% and the COD was 96 mg / l.
【0022】以上のようにして得た実施例3及び比較例
3における透過率及びCODの測定結果は、表3に示す
通りである。Table 3 shows the results of measuring the transmittance and COD in Example 3 and Comparative Example 3 obtained as described above.
【0023】[0023]
【表3】 [Table 3]
【0024】[0024]
【実施例4】染料としてバイエル社製のレバフィックス
染料124mg/l、チバガイギー社製のシバクロン染
料57mg/l、三菱化成ヘキスト社製のダイヤミラ染
料20mg/lを含有する各種反応性染料の混合廃液に
対して、以下の条件で行った。即ち、フェントン試薬と
して過酸化水素200mg/l、硫酸第一鉄7水塩80
mg/lを用い、酸化条件としては、酸化温度26〜3
0℃、酸化時間1.0時間、酸化槽のpH=2.7とし
た。また、アルミ系凝集剤としてポリ塩化アルミを30
0mg/l、凝結剤として水溶性ポリアミン樹脂を50
〜300mg/l、高分子凝集剤としてポリアクリルア
ミド(アニオン)を1mg/lとした。以上のような条
件下で、実施例1と同様の操作を行い、上澄み液につい
て透過率及びCODを測定した。但し、原液の透過率は
36%で、CODは43mg/lである。Example 4 A mixed waste liquid of various reactive dyes containing 124 mg / l of Levafix dye manufactured by Bayer, 57 mg / l of Cibacron dye manufactured by Ciba-Geigy, and 20 mg / l of Diamira dye manufactured by Mitsubishi Kasei Hoechst as dyes. On the other hand, it was performed under the following conditions. That is, hydrogen peroxide 200 mg / l, ferrous sulfate heptahydrate 80 as Fenton's reagent
Using mg / l, the oxidation conditions are oxidation temperature 26 to 3
The temperature was 0 ° C., the oxidation time was 1.0 hour, and the pH of the oxidation tank was 2.7. Moreover, polyaluminum chloride is used as an aluminum-based coagulant.
0 mg / l, 50% water-soluble polyamine resin as a coagulant
˜300 mg / l, and polyacrylamide (anion) as a polymer flocculant was 1 mg / l. Under the above conditions, the same operation as in Example 1 was performed, and the transmittance and COD of the supernatant liquid were measured. However, the transmittance of the stock solution is 36% and the COD is 43 mg / l.
【0025】実施例4との比較のために従来法による廃
水処理を以下の条件で行った。For comparison with Example 4, wastewater treatment by the conventional method was carried out under the following conditions.
【比較例4】即ち、染料としてバイエル社製のレバフィ
ックス染料124mg/l、チバガイギー社製のシバク
ロン染料57mg/l、三菱化成ヘキスト社製のダイヤ
ミラ染料20mg/lを含有する各種反応性染料の混合
廃液に対して、以下の条件で行った。即ち、フェントン
試薬として過酸化水素800mg/l、硫酸第一鉄7水
塩500mg/lを用い、酸化条件としては、酸化温度
30〜35℃、酸化時間2.5時間、酸化槽のpH=
3.0とした。以上のような条件下で、比較例1と同様
の操作を行い、上澄み液について透過率及びCODを測
定した。但し、原液の透過率は36%で、CODは43
mg/lである。[Comparative Example 4] Mixing of various reactive dyes containing 124 mg / l of Levafix dye manufactured by Bayer, 57 mg / l of Cibacron dye manufactured by Ciba-Geigy, and 20 mg / l of Diamira dye manufactured by Mitsubishi Kasei Hoechst as dyes. The waste liquid was treated under the following conditions. That is, hydrogen peroxide 800 mg / l and ferrous sulfate heptahydrate 500 mg / l were used as Fenton's reagent, and the oxidation conditions were as follows: oxidation temperature 30 to 35 ° C., oxidation time 2.5 hours, oxidation tank pH =
It was set to 3.0. Under the above conditions, the same operation as in Comparative Example 1 was performed, and the transmittance and COD of the supernatant liquid were measured. However, the stock solution has a transmittance of 36% and a COD of 43.
mg / l.
【0026】以上のようにして得た実施例4及び比較例
4における透過率及びCODの測定結果は、表4に示す
通りである。Table 4 shows the measurement results of the transmittance and COD in Example 4 and Comparative Example 4 obtained as described above.
【0027】[0027]
【表4】 [Table 4]
【0028】上記実施例結果より明らかであるように、
本発明は、フタロシアニン系等の反応性染料を含有する
難脱色性の染色廃水の脱色に、十分効果を発揮するもの
であり、また、COD除去にも優れた効果を発揮する。
更に、アゾ系の染色廃水では、より少ない薬品量で前記
効果を発揮し、また、各種反応性染料の混合廃液でも従
来法に比べ、より少ない薬品量で脱色効果、COD除去
効果を発揮する。As is clear from the results of the above embodiment,
INDUSTRIAL APPLICABILITY The present invention exerts a sufficient effect on the decolorization of dyeing wastewater which contains a reactive dye such as a phthalocyanine type and is difficult to decolor, and also exerts an excellent effect on COD removal.
Furthermore, in the case of azo dyeing wastewater, the above-mentioned effect is exhibited with a smaller amount of chemicals, and even with the mixed waste liquid of various reactive dyes, the decolorizing effect and the COD removing effect are exhibited with a smaller amount of chemicals as compared with the conventional method.
【0029】[0029]
【発明の効果】以上説明したように、本発明によれば、
反応性染料等の難脱色性染料を含有する染色廃水に対し
ても、従来のフェントン試薬法を用いた染色廃水処理法
に比べ、脱色、COD除去に優れた効果を発揮するもの
である。更に、薬品使用量の減少が図られることから、
経済的にも極めて優れるものである。As described above, according to the present invention,
Even for a dyeing wastewater containing a difficult-to-decolorize dye such as a reactive dye, it exhibits an excellent effect in decolorization and COD removal as compared with the conventional dyeing wastewater treatment method using the Fenton's reagent method. Furthermore, since the amount of chemicals used can be reduced,
It is also extremely economical.
【0030】[0030]
【図1】フェントン試薬法による従来の廃水処理法を表
した図である。FIG. 1 is a diagram showing a conventional wastewater treatment method by the Fenton reagent method.
【図2】本発明による廃水処理法を表した図である。FIG. 2 is a diagram showing a wastewater treatment method according to the present invention.
1 酸化槽 2 凝集槽 3 沈澱槽 4 中和槽 5 撹拌プロペラ 6 ポンプ 7 pH調整槽 8 薬品混合槽 9 凝集槽 1 Oxidation tank 2 Coagulation tank 3 Precipitation tank 4 Neutralization tank 5 Stirring propeller 6 Pump 7 pH adjusting tank 8 Chemical mixing tank 9 Coagulation tank
───────────────────────────────────────────────────── フロントページの続き (72)発明者 澤田 光男 京都府宮津市惣262番地 グンゼ株式会社 内 ─────────────────────────────────────────────────── ─── Continuation of front page (72) Inventor Mitsuo Sawada 262 Sou Sou, Miyazu City, Kyoto Prefecture Gunze Co., Ltd.
Claims (1)
素でpH≦3で酸化槽1にて酸化処理し、しかる後、該
処理液をpH調整槽7にてpH=6〜7に調整後、薬品
混合槽8にて該処理液にアルミ系凝集剤、凝結剤を添加
し、しかる後、凝集槽9にて高分子凝集剤を添加して凝
集沈澱により固液を分離除去することを特徴とする染色
廃水処理法。1. Dyeing wastewater is oxidized with hydrogen peroxide using iron salt as a catalyst at a pH ≦ 3 in an oxidation tank 1, and then the treated liquid is adjusted to pH = 6 to 7 in a pH adjusting tank 7. After the adjustment, an aluminum-based coagulant and a coagulant are added to the treatment liquid in the chemical mixing tank 8, and then a polymer coagulant is added in the coagulation tank 9 to separate and remove the solid liquid by coagulation precipitation. A method for treating dyeing wastewater, characterized by:
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JP4361819A JP2683991B2 (en) | 1992-12-17 | 1992-12-17 | Dyeing wastewater treatment method |
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Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5637097A (en) * | 1979-08-31 | 1981-04-10 | Ugine Kuhlmann | Method of refining waste water containing coloring agent |
-
1992
- 1992-12-17 JP JP4361819A patent/JP2683991B2/en not_active Expired - Fee Related
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---|---|---|---|---|
JPS5637097A (en) * | 1979-08-31 | 1981-04-10 | Ugine Kuhlmann | Method of refining waste water containing coloring agent |
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