JPS5980388A - Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter - Google Patents

Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter

Info

Publication number
JPS5980388A
JPS5980388A JP7831383A JP7831383A JPS5980388A JP S5980388 A JPS5980388 A JP S5980388A JP 7831383 A JP7831383 A JP 7831383A JP 7831383 A JP7831383 A JP 7831383A JP S5980388 A JPS5980388 A JP S5980388A
Authority
JP
Japan
Prior art keywords
treated
ammonia
precipitate
granulated slag
water
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
Application number
JP7831383A
Other languages
Japanese (ja)
Other versions
JPS6147573B2 (en
Inventor
Yoshimasa Igari
猪狩 俶将
Shoichiro Yokoyama
横山 正一郎
Yoshihiro Murao
村尾 好宥
Hirosaku Mukai
向 啓作
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.)
KANKYO GIJUTSU KAIHATSU KK
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
KANKYO GIJUTSU KAIHATSU KK
Agency of Industrial Science and Technology
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 KANKYO GIJUTSU KAIHATSU KK, Agency of Industrial Science and Technology filed Critical KANKYO GIJUTSU KAIHATSU KK
Priority to JP7831383A priority Critical patent/JPS5980388A/en
Publication of JPS5980388A publication Critical patent/JPS5980388A/en
Publication of JPS6147573B2 publication Critical patent/JPS6147573B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Water Treatment By Sorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Removal Of Specific Substances (AREA)

Abstract

PURPOSE:To obtain the titled agent for ammonia-contg. liquid matter disposal, by adding the specified amount of fine powdery magnesium hydroxide sludge after being dehydratively dried to the dry precipitate of water granulated slag after being treated with an acid. CONSTITUTION:Granulated slag from a steel-making furnace after being finely pulverized to at least 200-mesh is dissolved in an aqueous inorganic acid solution, and precipitate formed by making said solution alkaline is washed with water and dried to obtain dry precipitate. Said dry precipitate of granulated slag treated with an acid is mixed with dehydratively dried fine powdery magnesium hydroxide sludge at a wt. ratio of 1:1-5:1, and the mixture is baked at a temp. of 350-900 deg.C for 15min-2hr to obtain the agent for ammonia-contg. liquid matter disposal. When said treating agent is to be added to waste water, its addition ratio is 5-20 times the value of CODMn in the waste water.

Description

【発明の詳細な説明】 本発明はアンモニア含有液状物より同時にアンモニア、
 COD及び色を除去1−る綜合処理J11J及び該処
理剤を使用するアンモニア含有液状物よりアンモニア、
 COD及び色を同時に除去づ−るアンモニア含有液状
物綜合処理方法に関1−るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a method for simultaneously producing ammonia and
Ammonia,
This invention relates to an integrated treatment method for an ammonia-containing liquid material that simultaneously removes COD and color.

従来、排水、廃液等のCODの除去あるいは色の除去に
関しては多くの技術かあり、また続々としてその開発が
なされつつある。
Conventionally, there are many techniques for removing COD or color from waste water, waste liquid, etc., and they are being developed one after another.

−方、脱窒技術としてはたとえばアンモニアストリッピ
ング法、生物fヒ学的硝化・脱窒法1選択的イオン交換
法、不連続点塩素圧入処理法等があり、その中アンモニ
アストリッピング法にも各種の技術が展開されている。
-Denitrification techniques include, for example, ammonia stripping method, biological nitrification/denitrification method, selective ion exchange method, and discontinuous point chlorine injection treatment method. technology is being developed.

しかし排水、廃液あるいはその他の液状物中のアンモニ
ア、 COD及び色を同時に除去することは、従来困知
tであり、未だすぐれたしかも経済的な方法は存在しな
い。
However, it has not been known to simultaneously remove ammonia, COD and color from waste water, waste liquids or other liquids, and no good and economical method exists yet.

不発IJJ者らはかかる点に着目し、鋭意研究を重ねた
結果、本発明に到達したものであり、その要旨と1−る
ところは上記の如く排水、 F!A71iあるいはその
他の液状物中のアンモニア、 COD及び色を同時に除
去′1−8アンモニア含有液状物綜合処理剤並びに該剤
によるアンモニア含有液状物の綜合処理方法に存し、詳
しくは、少なくとも200メツシユ(C微粉化した製鉄
炉から得られる水砕スラグ(以下単に水砕スラグという
)を無機酸水浴液に溶解し、アルカリ水浴液をさらに添
加することにより該溶液をアルカリ性となし、析出した
沈澱物をP別、水洗し、ついで該水洗沈澱物を脱水乾燥
して得られた酸処理水砕スラグ乾燥沈澱物にさらに脱水
乾燥した微粉状水酸化マグネノウムスラツジを重量比に
て1:1乃至5:1の割合にて混加し、該混合物を35
0乃至900℃の温度にて15分乃至2時間焼成したア
ンモニア含有液状物綜合処叩剤に存し、さらに本発明の
要旨と1−るところは上記焼成酸処理水砕スラグ・水酸
化マグネシウムスラッジ処理剤を、被処理液状物中のC
ODMn量に対し5乃至20倍量にて該被処理液状物に
添加し、該添加被処理液状物中に空気あるいは水蒸気を
、上記被処理液状物中のCODMn量対上記処理剤の添
加率が上記比率内に維持されるような量で少な(とも1
時間通導し、ついで被処理液状物中の処1414剤をi
1別分離し、かくしてアンモニア計イーJ’ i&状!
吻よりアンモニア、COD及び色を同時に除去するアン
モニア含有液状物綜合処理方法に存する。
Unexploded IJJ people focused on this point and as a result of intensive research, they arrived at the present invention.The gist of the invention is as described above. Simultaneously removing ammonia, COD and color from A71i or other liquids' 1-8 An integrated treatment agent for ammonia-containing liquids and a method for the integrated treatment of ammonia-containing liquids using the agent. C. The pulverized granulated slag obtained from a steelmaking furnace (hereinafter simply referred to as granulated slag) is dissolved in an inorganic acid water bath solution, the solution is made alkaline by further adding an alkaline water bath solution, and the precipitated precipitate is removed. The acid-treated granulated slag dried precipitate obtained by washing the washed precipitate with water, and then dehydrating and drying the washed precipitate, was further dehydrated and dried with finely powdered magnesium hydroxide sludge in a weight ratio of 1:1 to 5. : 1, and the mixture was mixed at a ratio of 35
The present invention resides in an ammonia-containing liquid integrated beating agent calcined at a temperature of 0 to 900°C for 15 minutes to 2 hours, and the main feature of the present invention is to provide the above-mentioned calcined acid-treated granulated slag/magnesium hydroxide sludge. The processing agent is added to the C in the liquid to be processed.
It is added to the liquid to be treated in an amount of 5 to 20 times the amount of ODMn, and air or water vapor is added to the liquid to be treated, so that the amount of CODMn in the liquid to be treated is equal to the addition rate of the treatment agent. A small amount (both 1
1414 agent in the liquid material to be treated.
1 separate and thus the ammonia meter E J'i&!
The present invention provides an integrated treatment method for an ammonia-containing liquid that simultaneously removes ammonia, COD, and color from the proboscis.

本発明に於て使用されろ水砕スラグは製鉄炉から得られ
るスラグを急冷したものであり、例えば高炉水砕スラグ
の組成の1例を示せば第1表の通りである。
The granulated slag used in the present invention is obtained by rapidly cooling slag obtained from a steelmaking furnace, and an example of the composition of granulated blast furnace slag is shown in Table 1.

第  1  表 本発明に使用する水酸化マグネンウムスラノジ(通常約
60%含水〕は海水から水酸化マグネシウムを回収した
後のスラッジであり、その組成(絶乾状態)は第2表の
辿りである。
Table 1 Magnenium hydroxide sludge (usually about 60% water content) used in the present invention is the sludge obtained after recovering magnesium hydroxide from seawater, and its composition (absolutely dry state) is as shown in Table 2. It is.

第  2  表 水酸化マグネシウムスラッジ(通常的60%の含水〕の
脱水乾燥は通常の110℃、12時間の処理で行うこと
ができる。
Table 2 Magnesium hydroxide sludge (typically 60% water content) can be dehydrated and dried by a conventional treatment at 110° C. for 12 hours.

本発明に於て水砕スラグを溶解する無機酸としては例え
ばHCl 、 HNO3、H2SO4、I(C104等
が好ましく使用され、溶解温度室温あるいは100℃ま
での加温に於て水砕スラグを溶解した無機酸水溶液に添
加するアルカリ水浴液としては例えばNaOH。
In the present invention, as the inorganic acid for dissolving the granulated slag, for example, HCl, HNO3, H2SO4, I (C104, etc.) are preferably used, and the granulated slag is dissolved at a dissolution temperature of room temperature or heating up to 100°C. Examples of the alkaline water bath solution to be added to the inorganic acid aqueous solution include NaOH.

KOH、NH4OH、(NH2)2Co等の水溶液が使
用される。
Aqueous solutions of KOH, NH4OH, (NH2)2Co, etc. are used.

なお、無機酸水溶液としてはIN乃至5N水浴液が好ま
しく使用され、無機酸水浴液100+nI!に対し最高
152の割合で水砕スラグを添加するのが好ましい。
Incidentally, as the inorganic acid aqueous solution, an IN to 5N water bath solution is preferably used, and an inorganic acid water bath solution of 100+nI! Preferably, the granulated slag is added in a proportion of at most 152%.

本発明1(於て使用づ−る水砕スラグは少なくとも20
0メツシユに微粉化しjこものであるが、2〔用メツシ
ュ以上のものを使用すると無機酸に対する溶解性が低下
し、溶解残置が残ってしまうので好ましくない。
In the present invention 1, the granulated slag used is at least 20
Although it can be pulverized to 0 mesh, it is not preferable to use 2 mesh or more because the solubility in inorganic acids decreases and undissolved residue remains.

焼成温度については、350℃以下及び900℃以上で
あるといずれも焼成物の比表面イ1(か小さく、したが
って吸着反応性が低下する。
Regarding the firing temperature, if the temperature is 350° C. or lower and 900° C. or higher, the specific surface of the fired product will be small, and therefore the adsorption reactivity will decrease.

焼成時間については、焼成ン晶度と関係があり、焼成温
度9(川℃の場合は15分、350℃の場合2時間の焼
成時間が必狭である。
The firing time is related to the crystallinity of the firing, and the firing time is strictly limited to 15 minutes at a firing temperature of 9°C (15 minutes at 350°C and 2 hours at 350°C).

処理剤の添加割合については、排水中のCODMn量に
対して5乃至20倍量であり、排水中の有機物の含有量
との関係から得られたものであり、通常5乃至20倍量
であれば充分である。
The addition ratio of the treatment agent is 5 to 20 times the amount of CODMn in the wastewater, which was obtained from the relationship with the content of organic matter in the wastewater, and it is usually 5 to 20 times the amount of CODMn in the wastewater. It is sufficient.

空気、ちるいは水蒸気の通導量については、アンモニア
の除去と関連し、通導量は温度とpHにより支配され、
その場合上記添加址すなわち5乃至20倍量が維持でき
るように適宜決定されるものである。
Regarding the amount of conduction of air, dust, or water vapor, it is related to the removal of ammonia, and the amount of conduction is controlled by temperature and pH.
In that case, the above-mentioned addition amount, that is, 5 to 20 times the amount, is appropriately determined so as to be maintained.

以下に実施例を示し本発明をさらに詳#II K説明づ
−る。
The present invention will be explained in more detail below by way of examples.

実施例1 第1表に示1−約230メツツユに微粉化した高炉水砕
スラグ1007を4N −HC7水浴液10100Oに
加え、マダイ・チックスターラーを用いて200 r、
p、m。
Example 1 Granulated blast furnace slag 1007 shown in Table 1, pulverized to about 230 ml, was added to 10,100 O of a 4N-HC7 water bath, and heated at 200 r using a Madai tick stirrer.
p.m.

で攪拌して溶液を得、これに水1000rnlを添加し
、ついで4N −NaOH水溶液を徐々に加え浴液のp
Hを11.0とした。かくして析出した沈澱物をJT別
し、洗滌液のpHが7乃至8になるまで水洗し、該水洗
沈澱物を110℃にて約12時間乾燥して得られた・1
311!。
to obtain a solution, to which 1000rnl of water was added, and then a 4N-NaOH aqueous solution was gradually added to reduce the pH of the bath liquid.
H was set to 11.0. The precipitate thus precipitated was separated by JT, washed with water until the pH of the washing solution became 7 to 8, and the washed precipitate was dried at 110°C for about 12 hours to obtain 1.
311! .

成前の酸処理水砕スラグ乾燥沈澱・物Oζ脱水乾燥した
微粉状の水酸化マグネシウムスラッジを1=1の重量比
にて混加し、該混合物を400℃の温度にて1時間焼成
して焼成酸処理水砕スラグ・水酸化マグネンウムスラソ
ジ混合処理剤(AI)SMgS )をイ)jだ。
Acid-treated granulated slag dried precipitate and pre-formed dehydrated finely powdered magnesium hydroxide sludge were mixed at a weight ratio of 1=1, and the mixture was calcined at a temperature of 400°C for 1 hour. Calcined acid-treated granulated slag/magnenium hydroxide slurry mixed treatment agent (AI) SMgS) is a) j.

上記の如くにして得た処理剤(ADSMgS )による
(1)都市廃棄物埋立浸出水及び(2)活性汚泥処理糖
蜜廃水の処理は以下の通りである。
The treatment of (1) municipal waste landfill leachate and (2) activated sludge treated molasses wastewater using the treatment agent (ADSMgS) obtained as described above is as follows.

(1) pH7,70、CODMn764 ppm 、
色度1.244(457℃m吸光度〕及びアンモニア7
16 ppmの都市廃棄物埋立浸出水1000 mlに
対し、上記処理剤(ADS)を該浸出水中のCODMn
量に対し10倍縦添加し、約80℃にて該被処理液中1
℃留出液量が2 me/m i n VC/1′るよう
に水蒸気を1時間通導した。
(1) pH 7.70, CODMn 764 ppm,
Chromaticity 1.244 (457℃m absorbance) and ammonia 7
The above treatment agent (ADS) was added to 1000 ml of municipal waste landfill leachate containing 16 ppm CODMn in the leachate.
Add 10 times the amount vertically to the liquid to be treated at about 80°C.
Steam was passed through the reactor for 1 hour so that the amount of distillate at °C was 2 me/min VC/1'.

(2) pH7,53、CODM、 797 ppm 
、色Jf−1,835(457面吸光度〕及びアンモニ
ア795 ppmの活性汚泥処理糖蜜廃水を上記(りと
同一条件にて処理した。
(2) pH 7.53, CODM, 797 ppm
Activated sludge treated molasses wastewater with color Jf-1,835 (457 plane absorbance) and 795 ppm ammonia was treated under the same conditions as above.

結果は第3表の通りである。The results are shown in Table 3.

第3表 測定(lCて行った、 第3表の結果より焼成酸処理水砕スラグ・水酸化マグネ
シウムスラッジ混合処理剤はCODの除去、色度の低減
及びアンモニアの除去に才ぐれ、とくにアンモニアの除
去に顕著であった。
Measurements in Table 3 (conducted at 1C) The results in Table 3 show that the mixed treatment agent for calcined acid-treated granulated slag and magnesium hydroxide sludge is excellent at removing COD, reducing chromaticity, and removing ammonia. Removal was remarkable.

なお、処理剤の添加倍率ではX20がもっともよい結果
を示すが、処理後の処理剤のj°別等の点がらしてXI
O乃至X15が好ましい。
Regarding the addition ratio of the processing agent, X20 shows the best results, but considering the different j° of the processing agent after treatment, XI
O to X15 are preferred.

実施例2 実施例1に℃得られた焼成酸処理水砕スラグ′水酸化マ
グネシウムスラッジ混合処理剤(ADSMgS)を実施
例1の(2)に示す活性汚泥処理糖蜜廃水:301)m
l中のCODMo量に対し10倍量添加し、80℃のW
iA度にて該廃水中に900 ml’m1nの速度で空
気を1時間通導した。結果は第4表に示す辿りである。
Example 2 The calcined acid-treated granulated slag obtained in Example 1 and the magnesium hydroxide sludge mixed treatment agent (ADSMgS) were added to the activated sludge-treated molasses wastewater shown in (2) of Example 1: 301) m
Add 10 times the amount of CODMo in 1, and add it to W at 80°C.
Air was passed through the wastewater at a rate of 900 ml'mln for 1 hour at iA degrees. The results are as shown in Table 4.

第  4  表 第4表の結果より、焼成酸処理水砕スラグ・水酸化マグ
ネ/ウムスラソジ混合処理剤はCot)の除去、色度の
低減に1″ぐれ、とくにアンモニアの除去に於て顕著で
あった。
Table 4 From the results shown in Table 4, the calcined acid-treated granulated slag/magnesium hydroxide/umsurasodi mixed treatment agent showed a 1" difference in the removal of Cot) and the reduction of chromaticity, which was particularly noticeable in the removal of ammonia. Ta.

!侍許出願人 工業技術院長 川 1)裕 即問   
環境技術開発株式会社 代理人弁理士田代然治
! Chamberlain applicant Director of the Agency of Industrial Science and Technology Kawa 1) Yutaka Immediate question
Kenji Tashiro, Patent Attorney, Environmental Technology Development Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] (1)少なくとも200メツシユに微粉化した製鉄炉か
ら得られる水砕スラグを無機酸水溶液知溶解し、アルカ
リ水溶液をさらに添加することにより該溶液をアルカリ
性となし、析出した沈澱物をp別、水洗し、ついで該水
洗沈澱物を脱水乾燥して得られた酸処理水砕スラグ乾燥
沈澱物に、さらに脱水乾燥した微粉状水酸化マグ坏シウ
ムスラツジを重量此処てlコ1乃至5:1の割合にて混
加し、該混合物を350乃至900℃の温度にて15分
乃至2時間焼成し1こアンモニア含有液状物綜合処理剤
(1) Granulated slag obtained from a steelmaking furnace pulverized to at least 200 mesh is dissolved in an inorganic acid aqueous solution, the solution is made alkaline by further adding an alkaline aqueous solution, and the precipitated precipitate is separated by P and washed with water. Then, to the acid-treated granulated slag dried precipitate obtained by dehydrating and drying the water-washed precipitate, further dehydrated and dried fine powdered magnesium hydroxide sludge was added in a ratio of 1 to 5:1 by weight. The mixture was baked at a temperature of 350 to 900°C for 15 minutes to 2 hours to obtain an ammonia-containing liquid integrated treatment agent.
(2)少なくと%20I)メツシュに微粉化した製鉄炉
から得られ々水砕スラグを無機版木溶液に浴解し、アル
カリ水浴液をさらに添加することにより該溶液をアルカ
リ性となし、析出し1こ沈澱物を/jコ別、水洗し、つ
いで該水洗沈澱物を脱水乾燥して得られた酸処理水砕ス
ラグ乾燥沈澱物に、さらに脱水乾燥した微粉状の水酸化
マグネシウムスラッジをM量比にてl:l乃至5:1の
割合にて混加した混合物を350乃至900℃の温度に
て15分乃至2時間焼成した焼成混合物を、被処理液状
物中のCODM。 量に対し5乃至20倍量にて彼処3g2液状物に添加し
、該添加被処理状物中に空気あるいは水蒸気を、上記被
処理液状物中のCODMn量対上記添加物の添加率が上
記比率内に維持されるような量にて少なくとも1時間通
導し、ついで被処理液状物中の処理剤をf−1別分離し
、かくしてアンモニア含有液状物より、アンモニア、 
COD及び色を同時に除去するアンモニア含有液状物綜
合処理方法。
(2) At least 20 I) Granulated slag obtained from a steelmaking furnace pulverized into a mesh is bath-dissolved in an inorganic block solution, and the solution is made alkaline by further adding an alkaline water bath solution, and the precipitation is carried out. 1. The precipitate was washed separately with water, and then the washed precipitate was dehydrated and dried. M amount of dehydrated and dried fine powder magnesium hydroxide sludge was added to the acid-treated granulated slag dry precipitate obtained. CODM in the liquid material to be treated is obtained by baking a mixture mixed at a ratio of 1:1 to 5:1 at a temperature of 350 to 900° C. for 15 minutes to 2 hours. 5 to 20 times the amount of CODMn added to 3 g of the liquid material, and air or water vapor is added to the material to be treated, so that the amount of CODMn in the liquid material to be treated and the addition rate of the additive are as described above. The treatment agent in the liquid to be treated is separated by f-1, and thus ammonia, ammonia, and
A comprehensive treatment method for ammonia-containing liquids that simultaneously removes COD and color.
JP7831383A 1983-05-06 1983-05-06 Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter Granted JPS5980388A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7831383A JPS5980388A (en) 1983-05-06 1983-05-06 Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7831383A JPS5980388A (en) 1983-05-06 1983-05-06 Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP1342079A Division JPS598418B2 (en) 1979-02-09 1979-02-09 Ammonia-containing liquid material comprehensive treatment agent and the liquid material comprehensive treatment method

Publications (2)

Publication Number Publication Date
JPS5980388A true JPS5980388A (en) 1984-05-09
JPS6147573B2 JPS6147573B2 (en) 1986-10-20

Family

ID=13658444

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7831383A Granted JPS5980388A (en) 1983-05-06 1983-05-06 Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter

Country Status (1)

Country Link
JP (1) JPS5980388A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001085618A1 (en) * 2000-05-12 2001-11-15 Ok Soo Oh Method for treating wastewater with powders of slag generated from steel making process
KR100711757B1 (en) * 2000-12-22 2007-04-25 재단법인 포항산업과학연구원 Activated slag for treating wastewater and wastewater treating method using same

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001085618A1 (en) * 2000-05-12 2001-11-15 Ok Soo Oh Method for treating wastewater with powders of slag generated from steel making process
KR100345405B1 (en) * 2000-05-12 2002-07-24 오옥수 Method for treating waste water with steel slag
KR100711757B1 (en) * 2000-12-22 2007-04-25 재단법인 포항산업과학연구원 Activated slag for treating wastewater and wastewater treating method using same

Also Published As

Publication number Publication date
JPS6147573B2 (en) 1986-10-20

Similar Documents

Publication Publication Date Title
JP2003001218A (en) Method for treating waste having high chlorine and lead contents
CN110304703B (en) Preparation method for producing polyaluminium chloride water purifying agent by using aluminium ash
JP2002018395A (en) Treating method for waste
CN102531137B (en) Sulfide heavy metal chelating agent and preparation method thereof
JPS5980388A (en) Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter
CN113800549A (en) Method for extracting barium chloride from precipitated barium sulfate waste residue
JPS59166290A (en) Method for removing harmful component in waste water of smoke scrubbing
KR100318661B1 (en) Wastewater treatment agent and its treatment method
JPS598418B2 (en) Ammonia-containing liquid material comprehensive treatment agent and the liquid material comprehensive treatment method
JP2008143763A (en) Manufacturing method of titanium dioxide, calcium sulfate and iron oxide from waste acid generated in manufacturing process of titanium dioxide
JP4605754B2 (en) Method for treating silicon-containing wastewater, and flame-retardant heat insulating material and flame-retardant laminate using the product
JPS5980389A (en) Agent for comprehensive disposal of ammonia-contg. liquid matter and comprehensive disposal of said liquid matter
US1100675A (en) Process of eliminating iron from liquids.
JPS61171582A (en) Wet treatment of petroleum combusted ash
JPH0513718B2 (en)
JP5850294B2 (en) Waste disposal method
JPS6046930A (en) Improved method for treating heavy oil ash
JPH0435238B2 (en)
CN107698086B (en) Comprehensive treatment method of enzyme preparation industrial wastewater
JPS5881413A (en) Preparation of inorg. flocculant
JP2003236504A (en) Treatment method of waste containing selenium and chlorine component
JP2017060903A (en) Desalting method of burned ash
TWI443069B (en) Process for the preparation of six-valent iron
US1251564A (en) Method of treating water containing sulfuric acid and iron salts.
JP2005254119A (en) Flocculant and production method therefor