JP2002273457A - High-speed agitating reducing system - Google Patents
High-speed agitating reducing systemInfo
- Publication number
- JP2002273457A JP2002273457A JP2001075622A JP2001075622A JP2002273457A JP 2002273457 A JP2002273457 A JP 2002273457A JP 2001075622 A JP2001075622 A JP 2001075622A JP 2001075622 A JP2001075622 A JP 2001075622A JP 2002273457 A JP2002273457 A JP 2002273457A
- Authority
- JP
- Japan
- Prior art keywords
- water
- reducing agent
- ascorbic acid
- sodium
- mixing nozzle
- 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
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- Treatment Of Water By Oxidation Or Reduction (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、水道水・工業用水
・地下水・井戸水などに含まれるハロゲンイオンが過剰
酸化されて生成したハロゲン化酸を、除去する装置に関
する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an apparatus for removing halogenated acid generated by excessive oxidation of halogen ions contained in tap water, industrial water, groundwater, well water and the like.
【0002】[0002]
【従来の技術】ハロゲンイオンを含有する原水のオゾン
酸化処理によって、残留オゾン、あるいはハロゲン化酸
たとえば臭素酸イオン等の酸化物質が生成し、発ガン性
などに問題を引き起こす可能性がある。具体的には、例
えば、オゾン処理を行った水道水から、微量の臭素酸イ
オンが検出されるなど、ハロゲンイオンから、オゾン酸
化などにより有害な臭素酸イオンが生成し、その低減が
必要となっている。その解決策として、オゾン注入率の
制御や活性炭・生物活性炭処理による低減、アンモニア
添加オゾン酸化法等などの方法が採られてきた。2. Description of the Related Art Ozone oxidation treatment of raw water containing halogen ions produces residual ozone or oxidized substances such as halogenated acids such as bromate ions, which may cause problems in carcinogenicity. Specifically, for example, harmful bromate ions are generated from ozone oxidation and the like from halogen ions, such as detection of trace amounts of bromate ions from tap water that has been subjected to ozone treatment. ing. As a solution for this, methods such as control of the ozone injection rate, reduction by treatment with activated carbon and biological activated carbon, and an ammonia-added ozone oxidation method have been adopted.
【0003】一方、オゾンや塩素などを水に急速に混入
する装置が、米国特許第4019983号に開示されて
いる。On the other hand, an apparatus for rapidly mixing ozone, chlorine, and the like into water is disclosed in US Pat. No. 4,199,983.
【0004】[0004]
【発明が解決しようとする課題】オゾン注入率の制御
は、微量のハロゲン化酸の生成を抑えるためには理想的
な方法のひとつだが、微量であるが故にフィードバック
制御が困難であるという問題があった。The control of the ozone injection rate is one of the ideal methods for suppressing the generation of a small amount of halogenated acid. However, it is difficult to perform feedback control because of the small amount. there were.
【0005】また、活性炭の吸着作用と表面における還
元作用によるハロゲン化酸の除去方法は、活性炭が新し
い間は高い効力を維持できるが、生物活性炭では表面の
還元力が低下しやすいなど、吸着能力が下がったときに
は効力を維持できないという問題があった。The method of removing halogenated acid by the adsorption action of activated carbon and the reduction action on the surface can maintain a high efficiency while the activated carbon is new, but the bioactive carbon tends to have a reduced surface reducing power. However, there was a problem that the efficacy could not be maintained when the value fell.
【0006】アンモニア等の添加は、余剰薬剤の弊害が
予想されるという問題がある。[0006] The addition of ammonia or the like has a problem that the adverse effect of the surplus drug is expected.
【0007】そこで、前記酸化物質を確実に低減化でき
る装置が求められていた。[0007] Therefore, there has been a demand for an apparatus capable of reliably reducing the oxidized substance.
【0008】[0008]
【課題を解決するための手段】このような課題を解決す
るために、本発明の高速撹拌還元システムは、還元剤を
注入する薬品注入手段と、水を吹き出す水中ポンプと、
前記薬品注入手段および水中ポンプに接続し還元剤およ
び水を同時に吹き出す混合ノズルと、該混合ノズルから
吹き出された還元剤および水が乱流となって通過する反
応チューブとを備える。In order to solve such problems, a high-speed stirring reduction system of the present invention comprises a chemical injection means for injecting a reducing agent, a submersible pump for blowing water,
A mixing nozzle connected to the chemical injecting means and the submersible pump to simultaneously blow the reducing agent and water; and a reaction tube through which the reducing agent and water blown from the mixing nozzle pass as turbulent flows.
【0009】本発明の高速攪拌還元システムを用いるこ
とにより、攪拌翼などによる薬品の混合より、乱流によ
る強い攪拌の効果で、還元剤がハロゲン化酸と効率よく
接触することが可能となる。By using the high-speed stirring reduction system of the present invention, it is possible to bring the reducing agent into contact with the halogenated acid more efficiently due to the effect of strong stirring by turbulence than mixing of chemicals by a stirring blade or the like.
【0010】また、本発明のシステムは、水中ポンプや
ノズルなどの簡便な装置で効率よく処理を行うことがで
きるため、別途、薬品混合用の機械設備を設ける必要な
く、さらに、反応チューブを設けることにより、乱流の
拡散を防止して強い攪拌作用を維持することができるた
め、還元剤とハロゲン化酸とを安定して十分に接触させ
ることができ、未処理のハロゲン化酸の流出を確実に防
止することができる。[0010] Further, the system of the present invention can efficiently carry out the treatment with a simple device such as a submersible pump or a nozzle. Therefore, it is not necessary to separately provide a mechanical equipment for mixing chemicals, and further, a reaction tube is provided. This prevents the diffusion of the turbulent flow and maintains a strong stirring action, so that the reducing agent and the halogenated acid can be stably and sufficiently brought into contact with each other, and the outflow of untreated halogenated acid can be prevented. It can be prevented reliably.
【0011】前記還元剤は、亜硫酸水素ナトリウム、亜
硫酸ナトリウム、チオ硫酸ナトリウム、L−アスコルビ
ン酸、L−アスコルビン酸の塩、亜硫酸ガス、および亜
硫酸ガスと亜硫酸ナトリウムの混合物からなる群より選
ばれた1種以上であることが望ましい。The reducing agent is selected from the group consisting of sodium bisulfite, sodium sulfite, sodium thiosulfate, L-ascorbic acid, salts of L-ascorbic acid, sulfur dioxide, and a mixture of sulfur dioxide and sodium sulfite. Desirably more than species.
【0012】さらに、還元剤を添加する場合、pH調整
剤を加えることが好ましい。Further, when adding a reducing agent, it is preferable to add a pH adjuster.
【0013】[0013]
【発明の実施の形態】本発明の実施の形態を図面に基づ
いて説明する。図1は、本発明の高速撹拌還元システム
の一実施例を示すフロー図である。Embodiments of the present invention will be described with reference to the drawings. FIG. 1 is a flowchart showing one embodiment of the high-speed stirring reduction system of the present invention.
【0014】図1において、処理槽7は、流入水5aを
受け入れる流入口5を設けた第1槽と、処理水6aを排
出する流出口6を設けた第2槽とが、隔壁7aで区分さ
れている。In FIG. 1, a treatment tank 7 is divided into a first tank provided with an inlet 5 for receiving inflow water 5a and a second tank provided with an outlet 6 for discharging treated water 6a by a partition wall 7a. Have been.
【0015】本発明の高速撹拌還元システムは、処理槽
7の第1槽の中に、還元剤を注入する薬品注入手段1
と、水を吹き出す水中ポンプ2と、前記薬品注入手段お
よび水中ポンプに接続し、還元剤および水を同時に吹き
出す混合ノズル3とが設けられ、第2槽の中に、混合ノ
ズル3の吹き出す方向前方に配置され、隔壁7aに取り
付けられた反応チューブ4とを備える。The high-speed stirring reduction system according to the present invention comprises a chemical injection means 1 for injecting a reducing agent into a first tank of a processing tank 7.
And a mixing nozzle 3 connected to the chemical injecting means and the submersible pump and for simultaneously discharging the reducing agent and water. The mixing nozzle 3 is provided in the second tank in the front of the mixing nozzle 3 in the discharging direction. And the reaction tube 4 attached to the partition wall 7a.
【0016】第1槽内の処理水は、水中ポンプにより反
応チューブ内に噴出されるか、この噴出により誘引され
て反応チューブ内に流入する。The treated water in the first tank is jetted into the reaction tube by a submersible pump, or is attracted by this jet and flows into the reaction tube.
【0017】添加する還元剤は、亜硫酸水素ナトリウ
ム、亜硫酸ナトリウム、チオ硫酸ナトリウム、L−アス
コルビン酸およびその塩、亜硫酸ガス、亜硫酸ガスと亜
硫酸ナトリウムの混合物などを用いる。As the reducing agent to be added, sodium hydrogen sulfite, sodium sulfite, sodium thiosulfate, L-ascorbic acid and its salts, sulfur dioxide, a mixture of sulfur dioxide and sodium sulfite, etc. are used.
【0018】亜硫酸水素ナトリウム等の還元剤は、化学
量論的には酸化物質と当量で反応するので処理法として
確実であり、食品添加物として認められているので安全
である。A reducing agent such as sodium hydrogen sulfite reacts stoichiometrically with an oxidizing substance in an equivalent amount, so that it is reliable as a treatment method and is safe as it is recognized as a food additive.
【0019】第1槽へ流入口5から入る流入水5aは、
オゾン処理水等の臭素酸イオン等ハロゲン化酸を含むも
のであるが、これが本発明の高速攪拌還元システムによ
り、無害な臭素イオンに還元される。The inflow water 5a entering the first tank from the inflow port 5 is:
It contains a halogenated acid such as bromate ion such as ozonized water, which is reduced to harmless bromine ion by the high-speed stirring reduction system of the present invention.
【0020】さらに、オゾン処理水に含まれる残留オゾ
ンを還元剤で中和させることは、廃オゾン処理を触媒や
活性炭で実施する必要がなくなる意味からも、重要であ
る。Further, it is important to neutralize residual ozone contained in the ozonated water with a reducing agent from the viewpoint that it is not necessary to carry out waste ozone treatment with a catalyst or activated carbon.
【0021】[0021]
【実施例】以下に、本発明の一実施例について説明す
る。An embodiment of the present invention will be described below.
【0022】(実施例1)図1に示した前記処理槽7
に、水中ポンプを配置した。0.720mg−BrO3
/Lの臭素酸カリウム溶液を流入水5aとして導入し、
2.64mg/LのL−アスコルビン酸溶液を還元剤と
して添加したところ、臭素酸イオンは0.078mg−
BrO3/Lになった。モル濃度換算すると、5.02
μmol/LのBrO3を還元するのに、15.0μm
ol/Lのアスコルビン酸を要したことになり、臭素酸
イオン1molを除去するのに、3.0molのL−ア
スコルビン酸が必要であると計算できる。(Embodiment 1) The processing tank 7 shown in FIG.
, A submersible pump was placed. 0.720mg-BrO 3
/ L potassium bromate solution is introduced as influent water 5a,
When a 2.64 mg / L L-ascorbic acid solution was added as a reducing agent, the bromate ion was 0.078 mg-L.
BrO 3 / L. In terms of molarity, 5.02
15.0 μm to reduce μmol / L BrO 3
This means that ol / L ascorbic acid was required, and it can be calculated that 3.0 mol of L-ascorbic acid is required to remove 1 mol of bromate ions.
【0023】L−アスコルビン酸以外の還元剤、すなわ
ち亜硫酸水素ナトリウム、チオ硫酸ナトリウムおよび亜
硫酸ナトリウムについても、同様に臭素酸イオンの還元
剤添加による除去を行った。With respect to reducing agents other than L-ascorbic acid, that is, sodium bisulfite, sodium thiosulfate and sodium sulfite, bromate ions were similarly removed by adding a reducing agent.
【0024】表1に、結果を示す。Table 1 shows the results.
【0025】[0025]
【表1】 [Table 1]
【0026】臭素酸イオンとそれぞれの還元剤との間の
反応式は、つぎのとおりである。The reaction formula between the bromate ions and the respective reducing agents is as follows:
【0027】[0027]
【数1】 (Equation 1)
【数2】 (Equation 2)
【数3】 (Equation 3)
【数4】 (Equation 4)
【0028】亜硫酸ナトリウムでは、溶存酸素や空気中
酸素と反応するためかモル比が多少高めであったが、他
の還元剤では、ほぼ理論量の反応が起きた。In the case of sodium sulfite, the molar ratio was somewhat higher, probably because it reacts with dissolved oxygen or oxygen in the air. However, in the case of other reducing agents, almost the theoretical amount of reaction occurred.
【0029】(実施例2)実施例1と同様に、ヨウ素酸
イオン1molを除去するのに、3.0molのL−ア
スコルビン酸が必要であった。Example 2 As in Example 1, to remove 1 mol of iodate ions, 3.0 mol of L-ascorbic acid was required.
【0030】L−アスコルビン酸以外の還元剤について
も、実施例1と同様にヨウ素酸イオンの還元剤添加によ
る除去を行った。As for the reducing agents other than L-ascorbic acid, iodate ions were removed by adding the reducing agent in the same manner as in Example 1.
【0031】表1に、結果を示す。Table 1 shows the results.
【0032】(実施例3)実施例1と同様に、塩素酸イ
オン1molを除去するのに、3.0molのL−アス
コルビン酸が必要であった。Example 3 As in Example 1, 3.0 mol of L-ascorbic acid was required to remove 1 mol of chlorate ions.
【0033】L−アスコルビン酸以外の還元剤について
も、実施例1と同様に塩素酸イオンの還元剤添加による
除去を行った。As for the reducing agent other than L-ascorbic acid, chlorate ions were removed by adding the reducing agent in the same manner as in Example 1.
【0034】表1に、結果を示す。Table 1 shows the results.
【0035】(実施例4)図1に示した処理槽7に、純
水にオゾンガスを吹き込んだオゾン水を流入水5aとし
て導入し、表2に示した還元剤をそれぞれ添加し、還元
剤消費量を測定した。Embodiment 4 Ozone water obtained by blowing ozone gas into pure water is introduced into the treatment tank 7 shown in FIG. 1 as the inflow water 5a, and the reducing agents shown in Table 2 are added to reduce the consumption of the reducing agent. The amount was measured.
【0036】表2に、結果を示す。Table 2 shows the results.
【0037】[0037]
【表2】 [Table 2]
【0038】前述のハロゲン化酸との反応式で、チオ硫
酸ナトリウムのモル比が他の還元剤の2倍であるのと同
様の傾向である。オゾンも、ハロゲン化酸と同じく還元
剤とほぼ当量反応する。In the above reaction formula with a halogenated acid, the tendency is the same as when the molar ratio of sodium thiosulfate is twice that of the other reducing agents. Ozone reacts with the reducing agent in substantially the same amount as the halogenated acid.
【0039】[0039]
【発明の効果】本発明によれば、酸化処理後の水中のハ
ロゲン化酸、たとえば臭素酸イオンや、残留オゾンなど
を、確実に除去することが可能となる。加えて、使用す
る還元剤が食品添加物として認められている物質なの
で、上水に適用しても人体に安全である。酸化処理にオ
ゾン処理を行った場合でも、残留オゾンが低減できるの
で廃オゾン処理が不要となる。According to the present invention, it is possible to reliably remove halogenated acids, for example, bromate ions and residual ozone in water after the oxidation treatment. In addition, since the reducing agent used is a substance recognized as a food additive, it is safe for the human body even when applied to clean water. Even when ozone treatment is performed for the oxidation treatment, residual ozone can be reduced, so that waste ozone treatment is not required.
【0040】さらに、乱流による強い攪拌効果により、
還元剤がハロゲン化酸と効率よく接触することが可能と
なる。Furthermore, due to the strong stirring effect of the turbulence,
The reducing agent can efficiently contact the halogenated acid.
【0041】また、本発明のシステムは、水中ポンプや
ノズルなどの簡便な装置で効率よく処理を行うことがで
きるため、別途、薬品混合用の機械設備を設ける必要な
く、さらに、反応チューブを設けることにより、乱流の
拡散を防止して強い攪拌作用を維持することができるた
め、還元剤とハロゲン化酸とを安定して十分に接触させ
ることができ、未処理のハロゲン化酸の流出を確実に防
止することができる。Further, since the system of the present invention can efficiently carry out the treatment with a simple device such as a submersible pump or a nozzle, there is no need to separately provide a mechanical equipment for mixing chemicals, and further, a reaction tube is provided. This prevents the diffusion of the turbulent flow and maintains a strong stirring action, so that the reducing agent and the halogenated acid can be stably and sufficiently brought into contact with each other, and the outflow of untreated halogenated acid can be prevented. It can be reliably prevented.
【0042】これらにより、設備費、運転コストが軽減
できるばかりでなく、維持管理等の作業も軽減すること
ができる。Thus, not only the equipment cost and the operating cost can be reduced, but also the work such as maintenance and management can be reduced.
【図1】 本発明の高速撹拌還元システムの一実施例を
示す断面図である。FIG. 1 is a cross-sectional view showing one embodiment of a high-speed stirring reduction system of the present invention.
1 薬品注入手段 2 水中ポンプ 3 混合ノズル 4 反応チューブ 5 流入口 5a 流入水 6 流出口 6a 流出水 7 処理槽(第1槽、第2槽) 7a 隔壁 8 乱流域 DESCRIPTION OF SYMBOLS 1 Chemical injection means 2 Submersible pump 3 Mixing nozzle 4 Reaction tube 5 Inflow port 5a Inflow water 6 Outflow port 6a Outflow water 7 Treatment tank (1st tank, 2nd tank) 7a Partition wall 8 Turbulence area
───────────────────────────────────────────────────── フロントページの続き (72)発明者 新川 浩二 東京都港区芝浦3丁目6番18号 株式会社 西原環境衛生研究所内 Fターム(参考) 4D050 AA02 AA04 AB44 BA04 BA06 BA07 BC10 BD01 4G035 AB37 AC22 ────────────────────────────────────────────────── ─── Continued on the front page (72) Koji Shinkawa, Inventor F-term in Nishihara Environmental Sanitation Research Institute, 3-6-18, Shibaura, Minato-ku, Tokyo 4D050 AA02 AA04 AB44 BA04 BA06 BA07 BC10 BD01 4G035 AB37 AC22
Claims (2)
吹き出す水中ポンプと、前記薬品注入手段および水中ポ
ンプに接続し還元剤および水を同時に吹き出す混合ノズ
ルと、該混合ノズルから吹き出された還元剤および水が
乱流となって通過する反応チューブとを備えた高速撹拌
還元システム。1. A chemical injecting means for injecting a reducing agent, a submersible pump for blowing water, a mixing nozzle connected to the chemical injecting means and the submersible pump for simultaneously discharging the reducing agent and water, and a mixing nozzle blown out of the mixing nozzle. A high-speed stirring reduction system comprising a reaction tube through which a reducing agent and water pass in a turbulent manner.
亜硫酸ナトリウム、チオ硫酸ナトリウム、L−アスコル
ビン酸、L−アスコルビン酸の塩、亜硫酸ガス、および
亜硫酸ガスと亜硫酸ナトリウムの混合物からなる群より
選ばれた1種以上であることを特徴とする請求項1に記
載の高速撹拌還元システム。2. The method according to claim 1, wherein the reducing agent is sodium hydrogen sulfite,
2. The method according to claim 1, wherein the sulfite is at least one selected from the group consisting of sodium sulfite, sodium thiosulfate, L-ascorbic acid, salts of L-ascorbic acid, sulfur dioxide, and a mixture of sulfur dioxide and sodium sulfite. 2. The high-speed stirring reduction system according to 1.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012000604A (en) * | 2010-06-21 | 2012-01-05 | Sepa Sigma Inc | Rust prevention and rust prevention method for water supply pipe using pore dispersion apparatus |
KR101127420B1 (en) * | 2009-09-14 | 2012-03-22 | 주식회사 한국건설관리공사 | Structure for projecting chlorine of filtration plant |
-
2001
- 2001-03-16 JP JP2001075622A patent/JP2002273457A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101127420B1 (en) * | 2009-09-14 | 2012-03-22 | 주식회사 한국건설관리공사 | Structure for projecting chlorine of filtration plant |
JP2012000604A (en) * | 2010-06-21 | 2012-01-05 | Sepa Sigma Inc | Rust prevention and rust prevention method for water supply pipe using pore dispersion apparatus |
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