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JPS587357B2 - cyanobunkaihouhou - Google Patents
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JPS587357B2 - cyanobunkaihouhou - Google Patents

cyanobunkaihouhou

Info

Publication number
JPS587357B2
JPS587357B2 JP7771675A JP7771675A JPS587357B2 JP S587357 B2 JPS587357 B2 JP S587357B2 JP 7771675 A JP7771675 A JP 7771675A JP 7771675 A JP7771675 A JP 7771675A JP S587357 B2 JPS587357 B2 JP S587357B2
Authority
JP
Japan
Prior art keywords
cyanide
parts
hypochlorite
bromide
sodium
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.)
Expired
Application number
JP7771675A
Other languages
Japanese (ja)
Other versions
JPS52764A (en
Inventor
神屋公生
西川好行
藤墳成幸
野口幸雄
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.)
Fujifilm Wako Pure Chemical Corp
Original Assignee
Wako Pure Chemical Industries 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 Wako Pure Chemical Industries Ltd filed Critical Wako Pure Chemical Industries Ltd
Priority to JP7771675A priority Critical patent/JPS587357B2/en
Publication of JPS52764A publication Critical patent/JPS52764A/en
Publication of JPS587357B2 publication Critical patent/JPS587357B2/en
Expired legal-status Critical Current

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  • Removal Of Specific Substances (AREA)
  • Treatment Of Water By Oxidation Or Reduction (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)

Description

【発明の詳細な説明】 本発明はシアン又は金属と共存するシアンの著しく改良
された分解方法に係る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a significantly improved method for decomposing cyanide or cyanide coexisting with metals.

詳記すれば化学製品又は中間体製造工場、金属表面処理
工場、都市ガス製造工場、アンモニア合成工場等から排
出されようとするシアン又は金属と共存するシアン溶液
なる廃液、又はハロゲン化銀写真材料、青写真等の処理
液、分析用試薬溶液等、シアン又は金属と共存するシア
ン溶液に、次亜塩素酸ナトリウム、次亜塩素酸カリウム
、次亜塩素酸カルシウム等の次亜塩素酸塩と、水酸化ナ
トリウム、水酸化カリウム、炭酸ソーダ等のアルカリと
、臭素、臭化ナトリウム、臭化カリウム、臭化カルシウ
ム等、本発明の反応系に於いて臭素イオンを与える化合
物を添加する事を特徴とし、要すれば加熱して行うシア
ン又は金属と共存するシアンの分解方法に関する。
Specifically, cyanide or cyanide solutions coexisting with metals, which are being discharged from chemical product or intermediate manufacturing plants, metal surface treatment plants, city gas production plants, ammonia synthesis plants, etc., or silver halide photographic materials; Hypochlorites such as sodium hypochlorite, potassium hypochlorite, calcium hypochlorite, etc. are added to cyanide or cyanide solutions that coexist with metals, such as processing solutions for blueprints, analytical reagent solutions, etc., and water. It is characterized by adding an alkali such as sodium oxide, potassium hydroxide, and soda carbonate, and a compound that provides bromide ions in the reaction system of the present invention, such as bromine, sodium bromide, potassium bromide, and calcium bromide. This invention relates to a method for decomposing cyanide or cyanide coexisting with metal, which is carried out by heating if necessary.

従来これらシアン又は金属と共存するシアンを分解させ
るには、例えば「公害防止の技術と法規・水質編」(昭
和47年2月24日・第1刷・発行、監修・通商産業省
公害保安局、発行・社団法人産業公害防止協会)191
頁、[特開昭48−168941等に見られる如くアル
カリ塩素法が一般的に行なわれているが、これら次亜塩
素酸塩とアルカリとで該溶液中のシアンを分解させ無毒
化する従来法は、大量の次亜塩素酸塩を必要とし、特に
金属と共存する場合のシアンは屡々難分解性のシアノ錯
塩として存在し、これらのシアノ錯塩として存在してい
るシアンを分解させる為には、極めて大量の次亜塩素酸
塩を用い極めて酷烈な条件下で処理しなければならない
等の欠点があり、工業的規模の方法としては非常に不利
な方法であった。
Conventionally, in order to decompose these cyanides or cyanide that coexists with metals, for example, "Pollution Prevention Technology, Laws and Water Quality Edition" (February 24, 1970, 1st edition, published, supervised by Pollution Safety Bureau, Ministry of International Trade and Industry) , published by Industrial Pollution Control Association) 191
[Although the alkali chlorine method is generally practiced as seen in JP-A No. 48-168941, etc., the conventional method involves decomposing cyanide in the solution using hypochlorite and an alkali to detoxify it. requires a large amount of hypochlorite, and cyanide, especially when it coexists with metals, often exists in the form of difficult-to-decompose cyano complex salts. This method has drawbacks such as the need to use an extremely large amount of hypochlorite and to process under extremely harsh conditions, making it a very disadvantageous method on an industrial scale.

本発明者等は鋭意検討し、シアン又は金属と共存するシ
アンを、次亜塩素酸塩とアルカリを加えて分解させるに
際して、臭素又は本発明の反応系で臭素イオンを与える
化合物を添加し、少量の次亜塩素酸塩で緩和な条件で高
分解率で効果的に該シアンを分解させる工業的に有用な
本発明を完成した。
The present inventors have made extensive studies, and when cyanide or cyanide that coexists with metals is decomposed by adding hypochlorite and alkali, bromine or a compound that provides bromine ions in the reaction system of the present invention is added, and a small amount of cyanide is added. The present invention has been completed, which is industrially useful and effectively decomposes cyanide with a high decomposition rate under mild conditions using hypochlorite.

特に金属と共存することによってシアンが錯体となった
場合、その分解無毒化は極めて困難であるのに対し、臭
素イオンを僅量添加することによって、これが著しく容
易に達成されることは、全く驚くべきことである。
In particular, when cyanide forms a complex due to its coexistence with a metal, it is extremely difficult to decompose and detoxify it, but it is quite surprising that this can be accomplished extremely easily by adding a small amount of bromide ion. It is the right thing to do.

本発明に使用される次亜塩素酸塩としては、次亜塩素酸
ナトリウム、次亜塩素酸カリウム、次亜塩素酸カルシウ
ム等が挙げられ、それら次亜塩素酸塩の使用量は分解す
べきシアンが金属と共存するか否かとか、分解温度分解
時間等の諸条件により異なるが通常はシアンに対して理
論量の3倍以下で充分である。
Examples of the hypochlorite used in the present invention include sodium hypochlorite, potassium hypochlorite, calcium hypochlorite, and the like. Although it depends on various conditions such as whether cyanide coexists with the metal, decomposition temperature, decomposition time, etc., it is usually sufficient to use less than three times the theoretical amount of cyanide.

本発明に使用するアルカリとは水酸化ナトリウム、水酸
化カリウム、炭酸ソーダ、水酸化カルシウム、水酸化バ
リウム等であり、それらアルカリの量は、本発明方法の
反応を常にアルカリ性で行うことのできる量があれば足
りる。
The alkali used in the present invention includes sodium hydroxide, potassium hydroxide, soda carbonate, calcium hydroxide, barium hydroxide, etc., and the amount of the alkali is such that the reaction in the method of the present invention can always be carried out in an alkaline state. It is enough if there is.

本発明に使用される臭素イオンとは、本発明の反応系で
臭素イオンを与える化合物の事であり、臭素、臭化ナト
リウム、臭化カリウム、臭化カルシウム、臭化バリウム
、臭化アルミニウム等が挙げられる。
The bromide ions used in the present invention are compounds that provide bromide ions in the reaction system of the present invention, and include bromine, sodium bromide, potassium bromide, calcium bromide, barium bromide, aluminum bromide, etc. Can be mentioned.

これらの臭素イオンを与える化合物の使用量は、通常全
溶液量に対して5%以下で充分である。
The amount of the compound that provides these bromine ions used is usually 5% or less based on the total amount of the solution.

分解させる事が出来るシアンとしては、金属が共存しな
い場合のシアン及び、鉄、ニッケル、銅、亜鉛、銀、カ
ドミウム等の金属が共存している場合のシアンであり、
分解反応は常温に於いても十分進行するが、急速な処理
を望むなら50℃〜80℃で行なうのが好ましい。
Cyanide that can be decomposed includes cyanide when no metal coexists, and cyanide when metals such as iron, nickel, copper, zinc, silver, and cadmium coexist.
The decomposition reaction proceeds satisfactorily even at room temperature, but if rapid treatment is desired, it is preferably carried out at 50°C to 80°C.

本発明の利点は、緩和な条件でシアンを分解させる事が
出来るとか、通常は極めて分解し難い金属と共存するシ
アンを容易に分解させる事が出来る等の点にもあるが、
更に工業的利用に際して次亜塩素酸塩の使用量が少なく
て済む為、処理作業効率が良好であると共に原料費が安
くて済む等、工業的実施が非常に効果的、効率的に行な
われる点にある。
The advantages of the present invention include that cyanide can be decomposed under mild conditions, and that cyanide that coexists with metals that are normally extremely difficult to decompose can be easily decomposed.
Furthermore, since only a small amount of hypochlorite is required for industrial use, the processing efficiency is good and raw material costs are low, making industrial implementation very effective and efficient. It is in.

以下に実施例を述べ、本発明を更に説明する。Examples are given below to further explain the present invention.

実施例中、数量を表わす部は重量部である。In the examples, parts expressing quantities are parts by weight.

実施例 1 シアンをシアン根(CN−)として1000ppm含む
水溶液1000部に、13%の次亜鉛素酸ナトリウム水
溶液82部(理論量×1.5)と50%水酸化ナトリウ
ム水溶液10部と臭化ナトリウム2.5部を添加し、2
5℃で30分間加温する。
Example 1 To 1000 parts of an aqueous solution containing 1000 ppm of cyanide as a cyanide root (CN-), 82 parts of a 13% sodium subzinc chlorate aqueous solution (theoretical amount x 1.5), 10 parts of a 50% sodium hydroxide aqueous solution, and bromide were added. Add 2.5 parts of sodium,
Incubate at 5°C for 30 minutes.

分解の過程で発生する窒素ガス、炭酸ガス、塩酸ガス、
臭化水素ガス等の気体は、公知の方法により回収または
処理される。
Nitrogen gas, carbon dioxide gas, hydrochloric acid gas generated during the decomposition process,
Gases such as hydrogen bromide gas are recovered or treated by known methods.

分解反応終了後の溶液は無色澄明であり、含有シアン量
は0.1ppm(分解率100%と見做される)であっ
た。
The solution after the completion of the decomposition reaction was clear and colorless, and the amount of cyanide contained was 0.1 ppm (decomposition rate was considered to be 100%).

実施例 2 赤血塩をシアン根(CN−)として1000ppm含む
廃液1000部に、13%の次亜塩素酸ナトリウム水溶
液と50%水酸化ナトリウム水溶液と臭化ナトリウムを
下表の様に添加し反応させる。
Example 2 13% sodium hypochlorite aqueous solution, 50% sodium hydroxide aqueous solution and sodium bromide were added as shown in the table below to 1000 parts of waste liquid containing 1000 ppm of red blood salt as cyanide (CN-) and reacted. let

分解反応終了後の廃液は、沈澱物を分離回収し、上澄水
を排水として排出する。
After the completion of the decomposition reaction, the precipitate is separated and recovered from the waste liquid, and the supernatant water is discharged as waste water.

この上澄水は、無色澄明であり、含有シアン量は0.1
ppm以下(分解率100%)であった。
This supernatant water is clear and colorless, and contains 0.1 cyanide.
ppm or less (decomposition rate 100%).

実施例 3 Ni(CN)42−をCN根として1000ppm含む
廃液1000部に、13%NaClOを165部(Th
×3)50%水酸化ナトリウムを20部、臭化カリウム
を2.5部添加し、その後50℃で30分間加温する。
Example 3 165 parts of 13% NaClO (Th
x3) Add 20 parts of 50% sodium hydroxide and 2.5 parts of potassium bromide, and then heat at 50°C for 30 minutes.

以下実施例1と同様の処理を行なったところ、分解率は
100%であった。
Thereafter, the same treatment as in Example 1 was carried out, and the decomposition rate was 100%.

実施例 4 Cu(CN)43−をシアン根として1000ppm含
む廃液1000部に、13%NaClOを110部(T
h×2)、50%水酸化カリウムを20部、臭素を2.
5部添加し、その後25℃で2時間加温する。
Example 4 110 parts of 13% NaClO (T
h×2), 20 parts of 50% potassium hydroxide, and 2.0 parts of bromine.
Add 5 parts and then warm at 25° C. for 2 hours.

以下実施例1と同様の処理を行なったところ、分解率は
100%であった。
Thereafter, the same treatment as in Example 1 was carried out, and the decomposition rate was 100%.

実施例 5 Zn.(C.N)42−Fをシアン根として1000p
pm含む廃液1000部に次亜塩素酸カルシウムを13
.8部(Th×2)、水酸化カルシウムを20部、臭化
ナトリウムを2.5部添加し、その後50℃で30分間
加温する。
Example 5 Zn. (C.N) 1000p with 42-F as cyan root
Add 13 parts of calcium hypochlorite to 1000 parts of waste liquid containing PM.
.. 8 parts (Th×2), 20 parts of calcium hydroxide, and 2.5 parts of sodium bromide are added, and then heated at 50° C. for 30 minutes.

以下実施例1と同様の処理を行なったところ、分解率は
100%であった。
Thereafter, the same treatment as in Example 1 was carried out, and the decomposition rate was 100%.

Claims (1)

【特許請求の範囲】 1 シアンを含む系に、次亜塩素酸塩と、アルカリと、
臭素イオンを添加する事を特徴とするシアンの分解方法
。 2 シアンと金属を含む系に、次亜塩素酸塩と、アルカ
リと、臭素イオンを添加する事を特徴とするシアンの分
解方法。
[Claims] 1. A system containing cyanide, a hypochlorite, an alkali,
A cyanide decomposition method characterized by the addition of bromine ions. 2. A cyanide decomposition method characterized by adding hypochlorite, an alkali, and bromide ions to a system containing cyanide and metal.
JP7771675A 1975-06-24 1975-06-24 cyanobunkaihouhou Expired JPS587357B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7771675A JPS587357B2 (en) 1975-06-24 1975-06-24 cyanobunkaihouhou

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7771675A JPS587357B2 (en) 1975-06-24 1975-06-24 cyanobunkaihouhou

Publications (2)

Publication Number Publication Date
JPS52764A JPS52764A (en) 1977-01-06
JPS587357B2 true JPS587357B2 (en) 1983-02-09

Family

ID=13641601

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7771675A Expired JPS587357B2 (en) 1975-06-24 1975-06-24 cyanobunkaihouhou

Country Status (1)

Country Link
JP (1) JPS587357B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5714011A (en) * 1980-07-01 1982-01-25 Takechi Komusho Kk Manufacturing device for foundation pillar
JP7845135B2 (en) * 2022-09-28 2026-04-14 栗田工業株式会社 Treatment method for cyanide-containing wastewater

Also Published As

Publication number Publication date
JPS52764A (en) 1977-01-06

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