JPS63158200A - Dehydration of sludge - Google Patents
Dehydration of sludgeInfo
- Publication number
- JPS63158200A JPS63158200A JP61305778A JP30577886A JPS63158200A JP S63158200 A JPS63158200 A JP S63158200A JP 61305778 A JP61305778 A JP 61305778A JP 30577886 A JP30577886 A JP 30577886A JP S63158200 A JPS63158200 A JP S63158200A
- Authority
- JP
- Japan
- Prior art keywords
- sludge
- polymer flocculant
- flocculant
- organic polymer
- amphoteric
- 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
- 239000010802 sludge Substances 0.000 title claims abstract description 38
- 230000018044 dehydration Effects 0.000 title description 20
- 238000006297 dehydration reaction Methods 0.000 title description 20
- 229920000620 organic polymer Polymers 0.000 claims abstract description 30
- 238000000034 method Methods 0.000 claims abstract description 16
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 150000001450 anions Chemical class 0.000 claims description 7
- 150000001768 cations Chemical class 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 17
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 abstract description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract description 6
- 235000011121 sodium hydroxide Nutrition 0.000 abstract description 6
- 239000000446 fuel Substances 0.000 abstract description 5
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 abstract description 3
- 239000000920 calcium hydroxide Substances 0.000 abstract description 3
- 235000011116 calcium hydroxide Nutrition 0.000 abstract description 3
- 229910001861 calcium hydroxide Inorganic materials 0.000 abstract description 3
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 abstract description 2
- 239000004744 fabric Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 abstract description 2
- 235000011118 potassium hydroxide Nutrition 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 20
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 12
- 239000002245 particle Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 125000002091 cationic group Chemical group 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- 239000008394 flocculating agent Substances 0.000 description 7
- 239000010865 sewage Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 6
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- 238000010979 pH adjustment Methods 0.000 description 6
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
- -1 and among these Substances 0.000 description 4
- 239000010800 human waste Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 238000005189 flocculation Methods 0.000 description 3
- 230000016615 flocculation Effects 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000004448 titration Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010842 industrial wastewater Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000005416 organic matter Substances 0.000 description 2
- 239000003002 pH adjusting agent Substances 0.000 description 2
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 2
- 229910052939 potassium sulfate Inorganic materials 0.000 description 2
- 235000011151 potassium sulphates Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229950003937 tolonium Drugs 0.000 description 2
- HNONEKILPDHFOL-UHFFFAOYSA-M tolonium chloride Chemical compound [Cl-].C1=C(C)C(N)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 HNONEKILPDHFOL-UHFFFAOYSA-M 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000002351 wastewater Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229920001661 Chitosan Polymers 0.000 description 1
- 229910021578 Iron(III) chloride Inorganic materials 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 108091047102 miR-4 stem-loop Proteins 0.000 description 1
- 108091049748 miR-4-1 stem-loop Proteins 0.000 description 1
- 108091058497 miR-4-2 stem-loop Proteins 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Treatment Of Sludge (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、下水、し尿処理場、有機性産業排水等より生
じる有機質汚泥を効率的に処理する汚泥の脱水力法に関
する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a sludge dehydration method for efficiently treating organic sludge generated from sewage, human waste treatment plants, organic industrial wastewater, etc.
従来より、下水、し尿処理場及び有機性産業排水等より
生じる有機質汚泥は、高分子凝集剤を添加し℃スクリュ
ーデカンター、ベルトプレス等で脱水する処理方法が採
用され℃いる。Conventionally, organic sludge generated from sewage, human waste treatment plants, organic industrial wastewater, etc. has been treated by adding a polymer flocculant and dewatering it using a screw decanter, a belt press, or the like.
脱水処理された汚泥(以下「脱水ケーキ」という)は埋
め立て等に用いられることもあるが、主に焼却処分され
る。Dehydrated sludge (hereinafter referred to as "dehydrated cake") is sometimes used for landfill, etc., but is mainly disposed of by incineration.
焼却において脱水ケーキ中の水分の蒸発に燃料の大部分
が使用され、一般に脱水ケーキ中の水分が1%低下する
と燃料の10%程度が節約可能である。In incineration, most of the fuel is used to evaporate the moisture in the dehydrated cake, and generally, if the moisture in the dehydrated cake decreases by 1%, about 10% of the fuel can be saved.
しかるに、近年水処理の高度化、水処理対象排水の性状
の変化、多様化等により汚泥が脱水し難い性状のものと
なって焼却処分における燃料費が増大しており、脱水ケ
ーキの低含水率化が要望されている。However, in recent years, due to the advancement of water treatment, changes in the properties of wastewater to be treated, and diversification, etc., sludge has become difficult to dehydrate, resulting in increased fuel costs for incineration. It is requested that the
有機質汚泥は
イ、 SS粒子径が小さく、強度が弱い、更に低比重で
あること
口、R水性であり、多量の内部保留水、表面付着水を含
有していること
ノ・、腐敗性有機物を含有し、粘着性が強いことからそ
のままでは殆ど脱水することができず、通常は有機系高
分子凝集剤を添加し℃スクリューデカンター、ベルトプ
レス、スクリュープレス等の汚泥脱水機で脱水処理され
ている。Organic sludge has a small SS particle size, weak strength, and low specific gravity; it is water-based; it contains a large amount of internally retained water and water attached to the surface; and it contains no putrefying organic matter. Because of its strong adhesion, it is almost impossible to dehydrate it as it is, and it is usually dehydrated by adding an organic polymer flocculant and using a sludge dewatering machine such as a °C screw decanter, belt press, or screw press. .
しかし、汚泥の性状にも依るが、これらの方法では脱水
ケーキの含水率を充分に低下させることができない。However, depending on the properties of the sludge, these methods cannot sufficiently reduce the water content of the dehydrated cake.
また、最近、下水処理施設においても分流式の流入方式
が増加しているために汚泥中の有機質が増加する傾向に
あり、特にベルトプレス型脱水機を用いた場合ベルトか
らの脱水ケーキの剥離が不良となり、この為含水率を比
較的高い状態で脱水を止めなければならない秋況にある
。In addition, recently, there has been an increase in the use of separate flow systems in sewage treatment facilities, which has resulted in an increase in organic matter in sludge, and in particular when using a belt press type dehydrator, peeling of the dewatered cake from the belt is becoming more difficult. Because of this, we are now in a situation where we have to stop dehydration while keeping the moisture content relatively high.
これらの問題点を解消するものとして無機凝集剤と有機
高分子凝集剤を併用する方法(特開昭58−51998
号公報及び特開rIB59−16599号公報等)が提
案され【いる。A method of using an inorganic flocculant and an organic polymer flocculant in combination to solve these problems (Japanese Patent Laid-Open No. 58-51998
No. 4, Japanese Unexamined Patent Publication No. RIB59-16599, etc.) have been proposed.
特開昭58−51998号公報にはポリ硫酸鉄(無機凝
集剤)と有機高分子凝集剤を併用し有機高分子凝集剤と
してノニオン性、アニオン性もしくはカチオン性のもの
を単独で使用する方法が記載されているものの、この方
法では生成するフロックの粒径は概し工小さくて強度が
不充分で脱水ケーキは塊状になり易いため脱水ケーキの
含水率を低下させることが困難である。JP-A No. 58-51998 discloses a method in which polyferric sulfate (an inorganic flocculant) and an organic polymer flocculant are used in combination, and a nonionic, anionic or cationic organic polymer flocculant is used alone. Although this method is described, the particle size of the flocs produced by this method is generally small and has insufficient strength, and the dehydrated cake tends to form lumps, making it difficult to reduce the moisture content of the dehydrated cake.
また、特開昭59−16599号公報には無機凝集剤と
有機高分子凝集剤を併用し、しかも有機高分子凝集剤と
してポリアクリルアミド系ポリマーのマンニッヒ変性物
(カチオン性)とアニオン性有機高分子凝集剤を用いる
方法が記載されているものの、この方法では脱水ケーキ
の炉布剥離性が不充分である場合が多く脱水ケーキの含
水率低下も困難である。In addition, JP-A-59-16599 discloses that an inorganic flocculant and an organic polymer flocculant are used in combination, and as the organic polymer flocculant, a Mannich modified product (cationic) of a polyacrylamide polymer and an anionic organic polymer are used. Although a method using a coagulant has been described, in many cases, the removability of the dehydrated cake from the furnace cloth is insufficient, and it is also difficult to reduce the moisture content of the dehydrated cake.
本発明の目的は、これらの問題点を解消し、生成するフ
ロックが充分な大きさの粒径と強度を有し、脱水ケーキ
の含水率が低(て炉布剥離性が良好な汚泥の脱水方法を
提供することにある。The purpose of the present invention is to solve these problems, to ensure that the generated flocs have sufficient particle size and strength, and that the water content of the dewatered cake is low (and that the dewatering cake of sludge has good removability). The purpose is to provide a method.
本発明の要旨は、無機凝集剤添加後のpH値が5〜8で
ある有機質汚泥に対して両性有機高分子凝集剤を添加し
、次いで脱水することを特徴とする汚泥の脱水方法にあ
る。The gist of the present invention resides in a method for dewatering sludge, which comprises adding an amphoteric organic polymer flocculant to organic sludge whose pH value after addition of the inorganic flocculant is 5 to 8, and then dewatering the organic sludge.
本発明において、有機質汚泥とは高BOD排水の生物処
理等により発生する汚泥をいい、その例としては下水、
し尿処理場で発生する汚泥、食品工業、化学工業等にお
いて発生する汚泥等を挙げることが出来る。In the present invention, organic sludge refers to sludge generated through biological treatment of high BOD wastewater, examples of which include sewage,
Examples include sludge generated in human waste treatment plants, sludge generated in the food industry, chemical industry, etc.
本発明において、無機系凝集剤としては、硫酸バンド、
塩化第二鉄、硫酸第一鉄、ポリ硫酸鉄等公知のものを用
いることができるが、このなかでは鉄系の無機凝集剤が
好ましい。In the present invention, as the inorganic flocculant, sulfuric acid bandate,
Known agents such as ferric chloride, ferrous sulfate, and polyferrous sulfate can be used, but iron-based inorganic flocculants are preferred among these.
無機凝集剤添加後の有機質汚泥のpH値は5〜8の範囲
であることが必要であり、pi(値がこの範囲より小さ
い場合やこの範囲を越える場合は両性有機高分子凝集剤
を加えてフロックを生成させたときのフロックの径が小
さく、甚だしい場合は全く凝集せず、従って脱水効率が
著しく低下しあるいは全く脱水できないので好ましくな
い。The pH value of organic sludge after adding an inorganic flocculant must be in the range of 5 to 8, and if the pi (value is smaller than or exceeds this range, add an amphoteric organic polymer flocculant. When the flocs are generated, the diameter of the flocs is small, and in extreme cases, they do not coagulate at all, and therefore the dewatering efficiency is significantly reduced or dewatering is not possible at all, which is not preferable.
無機凝集剤添加後のp)I値が5〜8の範囲にある場合
は特にpHMir4整を必要としないが、それ以外の場
合はアルカリ又は酸によりてpH調整する。If the p)I value after addition of the inorganic flocculant is in the range of 5 to 8, pH Mir4 adjustment is not particularly required, but in other cases, the pH is adjusted with an alkali or acid.
アルカリとして苛性ソーダ、苛性カリ、消石灰、アンモ
ニア等を用いることができるが、この中では苛性ソーダ
、消石灰が好ましい。Caustic soda, caustic potash, slaked lime, ammonia, etc. can be used as the alkali, and among these, caustic soda and slaked lime are preferred.
また酸として硫酸、塩酸、酢酸、スルファミン酸等を用
いることができるが、この中で硫酸、塩酸が好ましい。Further, as the acid, sulfuric acid, hydrochloric acid, acetic acid, sulfamic acid, etc. can be used, and among these, sulfuric acid and hydrochloric acid are preferred.
このpH値は6〜7であることがより好ましい。More preferably, this pH value is 6-7.
また、無1機凝集剤を然加したときの反応時間及びpH
調整に要する時間は特に考πを必要とせず、無機凝集剤
の添加、pH′?A整、両性有機高分子凝集剤の添加を
順次行なえばよい。Also, the reaction time and pH when an inorganic flocculant is added
There is no need to consider the time required for adjustment, and the addition of an inorganic flocculant and the pH'? A adjustment and addition of the amphoteric organic polymer flocculant may be carried out sequentially.
本発明において用いられる両性有機高分子凝集剤とは、
分子内にアニオン性基としてカルボキシル基、スルホン
基又はこれらの塩等を有し、カチオン性基として第三級
アミン、その中和塩、四級塩等を有する高分子凝集剤を
いい、これらのイオン性成分の他にノニオン性成分が含
まれているものでありてもよい。The amphoteric organic polymer flocculant used in the present invention is:
A polymer flocculant that has a carboxyl group, sulfone group, or a salt thereof as an anionic group in the molecule, and a tertiary amine, its neutralized salt, quaternary salt, etc. as a cationic group. It may contain a nonionic component in addition to the ionic component.
これらの中では水中での溶解性能、凝集性能等の点から
アニオン性基としてカルボキシル基又はその塩を有する
両性有機高分子凝集剤が好ましい。Among these, amphoteric organic polymer flocculants having a carboxyl group or a salt thereof as an anionic group are preferred from the viewpoint of solubility in water, flocculation performance, etc.
本発明において特に好ましく用いられる両性有機高分子
凝集剤を構成するカチオン性のモノマ一単位としてはジ
メチルアミノエチル(メタ)アクリレート、ジエチルア
ミノエチル(メタ)アクリレート、ジメチルアミンプロ
ピル(メタ)アクリルアミド、ジエチルアミノプロピル
(メタ)アクリルアミド、アリルジメチルアミンもしく
はこれらの中和塩、四級塩等を、アニオン性のモノマー
阜位としてはアクリル酸、メタクリル酸もしくはこれら
のアルカリ金属塩等を挙げることができ、又ノニオン性
のモノマ一単位としては(メタ)アクリルアミド、N、
N−ジメチル(メタ)アクリルアミド、N、N−ジエチ
ル(メタ)アクリルアミド等を挙げることができる。Examples of the cationic monomer unit constituting the amphoteric organic polymer flocculant particularly preferably used in the present invention include dimethylaminoethyl (meth)acrylate, diethylaminoethyl (meth)acrylate, dimethylaminepropyl (meth)acrylamide, and diethylaminopropyl (meth)acrylate. Examples of anionic monomers include acrylic acid, methacrylic acid, and alkali metal salts thereof; As a monomer unit, (meth)acrylamide, N,
Examples include N-dimethyl (meth)acrylamide and N,N-diethyl (meth)acrylamide.
本発明で用いられる両性有機高分子凝集剤においてカチ
オン当量値Cv、アニオン当量値Aマは特に限定されな
いが、汚泥に添加する前の溶解槽での水中溶解性、汚泥
の凝集性能、凝集フロックの脱水性を考慮すると、カチ
オン当量値Cv が1. O〜4. Omeq/ J
’ 、 アニオン当量値Avが0.3〜2. Ome
q / J’ 、 Cv/ Av の比が1.5〜
8.0程度の範囲にあるものが好まし、く、カチオン当
量値Cv が1.3〜3.8 meq/J’、アニオン
当量値Avが0.4〜1.8 meq7’7 、 C
v/ Ayの比が1.8〜7.0の範囲にあるものがよ
り好ましい。The cation equivalent value Cv and anion equivalent value A of the amphoteric organic polymer flocculant used in the present invention are not particularly limited, but include solubility in water in a dissolution tank before addition to sludge, flocculation performance of sludge, and flocculation Considering dehydration, the cation equivalent value Cv is 1. O~4. Omeq/J
', the anion equivalent value Av is 0.3 to 2. Ome
q/J', Cv/Av ratio is 1.5~
Those in the range of about 8.0 are preferable, and the cation equivalent value Cv is 1.3 to 3.8 meq/J', and the anion equivalent value Av is 0.4 to 1.8 meq7'7, C
It is more preferable that the v/Ay ratio is in the range of 1.8 to 7.0.
本発明において、前記の両性高分子凝集剤のカチオン当
量値Cvおよびアニオン当量値Avは以下に示すコロイ
ド滴定法によりて求めることができる。In the present invention, the cation equivalent value Cv and anion equivalent value Av of the amphoteric polymer flocculant can be determined by the colloid titration method shown below.
(1) カチオン当量値の測定
■、 コニカルビーカーに脱イオン水9011!jをと
り、試料500 ppm溶液1011tを加え、塩酸水
溶液でpHを3.0とし、約1分間攪拌する。次に、ト
ルイジンブルー指示薬を2〜3滴加え、N/400−ポ
リビニル硫酸カリウム試薬(N/4QO−PVSK)で
滴定する。(1) Measurement of cation equivalent value■, Deionized water 9011 in a conical beaker! 1,011 t of a 500 ppm sample solution was added, the pH was adjusted to 3.0 with an aqueous hydrochloric acid solution, and the mixture was stirred for about 1 minute. Next, add 2-3 drops of toluidine blue indicator and titrate with N/400-polyvinyl potassium sulfate reagent (N/4QO-PVSK).
滴定速度は2ゴ/分とし、検水が青から赤紫色に変色、
10秒間以上保持する時点を終点とする。The titration rate was 2g/min, and the sample water changed color from blue to reddish-purple.
The end point is when the sample is held for 10 seconds or more.
■、試料500 ppm水溶液の調製
試料0,2P(乾品換算しない)を精秤し、共栓付三角
コルベンにとり、脱イオン水100mA!で溶解する。■Preparation of sample 500 ppm aqueous solution Precisely weigh samples 0 and 2P (not converted to dry product), transfer to a triangular container with a stopper, and add deionized water at 100 mA! Dissolve with.
この25m1を100rnlメスフラスコにて脱イオン
水でメスアップする。Make up 25 ml of this volume with deionized water in a 100 rnl volumetric flask.
1、計算法
カチオン当量値(meq/ P )
(2) アニオン当量値の測定
■、 コニカルビーカーに脱イオン水9Qmlをとり、
N/1〇−苛性ソーダ水溶液0.5dを加え、攪拌下N
/200−メチルグリコールキトサン試液5−を滴下し
、1分間以上攪拌する。次に、試料の500 ppm水
溶液101をゆっくり滴下し、滴下後さらに5分間以上
攪拌した後、トルイジンブルー指示薬を2〜3m加え、
N/’400−ポリビニル硫酸カリウム試薬(N/40
0−PVSK)で滴定する。1. Calculation method: Cation equivalent value (meq/P) (2) Measurement of anion equivalent value ■: Take 9Qml of deionized water in a conical beaker,
N/1〇- Add 0.5 d of caustic soda aqueous solution, and add N while stirring.
/200-Methyl glycol chitosan test solution 5- is added dropwise and stirred for 1 minute or more. Next, a 500 ppm aqueous solution 101 of the sample was slowly added dropwise, and after being stirred for 5 minutes or more, 2 to 3 m of toluidine blue indicator was added.
N/'400-polyvinyl potassium sulfate reagent (N/40
0-PVSK).
滴定速度は”l rttl /分とし、検水が青から赤
紫色に変色、10秒間以上保持する時点を終点・とする
。The titration rate is 1 rttl/min, and the end point is when the sample water changes color from blue to reddish-purple and remains for 10 seconds or more.
なお、上記操作に於いて、試料を添加しない場合をブラ
ンク試験とする。In addition, in the above operation, the case where no sample is added is considered as a blank test.
■、試料の500 ppm水溶液の調製試料0.171
(乾品換算しない)を精秤し、共栓付三角コルベンにと
り、脱イオン水Zoo―に溶解する。この50mを10
0Mメスフラスコにて脱イオン水でメスアップする。■, Preparation sample of 500 ppm aqueous solution of sample 0.171
Weigh accurately (not calculated as dry product), transfer to a triangular kolben with a stopper, and dissolve in deionized water Zoo-. This 50m is 10
Make up to volume with deionized water in a 0M volumetric flask.
■、計算法
・アニオン当量値(meq/J’)
本発明においては両性有機高分子凝集剤を添加し、フロ
ックを形成させた後、公知の手法により脱水されるが、
脱水機としては、たとえばスクリュープレス型脱水機、
フィルタープレス型脱水機、ベルトプレス型脱水機、ス
クリューデカンタ−等を使用することができる。(2) Calculation method/Anion equivalent value (meq/J') In the present invention, an amphoteric organic polymer flocculant is added to form flocs, and then dehydrated by a known method.
Examples of dehydrators include screw press type dehydrators,
A filter press type dehydrator, belt press type dehydrator, screw decanter, etc. can be used.
以下、実施例により本発明を具体的に説明する。 Hereinafter, the present invention will be specifically explained with reference to Examples.
尚、実施例において、有機高分子凝集剤は第1表に示す
ものを使用し、無機凝集剤は10重量%水溶液として、
有機高分子凝集剤は0.5重量%の水溶液として使用し
た。又、これらの凝集剤の添加量はいずれも汚泥中のS
Sに対する重ft%として表示した。In the examples, the organic polymer flocculants shown in Table 1 were used, and the inorganic flocculants were prepared as a 10% by weight aqueous solution.
The organic polymer flocculant was used as a 0.5% by weight aqueous solution. In addition, the amount of these flocculants added depends on the amount of S in the sludge.
Expressed as weight % of S.
実施例1及び2
pH;6,4、SS;2,0%、灼熱域g、(以下「V
TsJという);75,1%、M−7#力IJ度; 6
35 m9/lなる性状のし尿余剰汚泥に対して、第2
表に示す種類と量の無機凝集剤を添加して約2分間攪拌
後、水酸化ナトリウム液を添加してpHを6.0とした
。Examples 1 and 2 pH; 6,4, SS; 2,0%, scorching range g, (hereinafter "V
TsJ); 75.1%, M-7# force IJ degree; 6
For human waste surplus sludge with properties of 35 m9/l, the second
After adding the type and amount of inorganic flocculant shown in the table and stirring for about 2 minutes, sodium hydroxide solution was added to adjust the pH to 6.0.
pH調整開始から2分後に両性高分子凝集剤R−1を各
々1.6%添加してフロックを生成させ、スクリューデ
カンタ−により脱水試験を行なった。いずれの場合も生
成したフロックは充分な太き毬と強度を有しており、脱
水ケーキはフレーク状で粘着性が少なくケーキ含水率、
SS回収率共に良好な結果が得られた。Two minutes after the start of pH adjustment, 1.6% of each amphoteric polymer flocculant R-1 was added to form flocs, and a dehydration test was conducted using a screw decanter. In either case, the floc produced has sufficient thickness and strength, and the dehydrated cake is flaky and has little stickiness, and the moisture content of the cake is low.
Good results were obtained in terms of SS recovery rate.
比較例1及び2
有機高分子凝集剤として、比較例1ではカチオン性のに
−2を、比較例2ではアニオン性のA−1を用い、その
他の条件は実施例1と全く同様にして脱水試験を行なっ
たところ、第2表に示すように、両比較例共脱水ケーキ
は塊状でケーキ含水率は高く、実施例1と比較すると著
しく悪い性能を示した。Comparative Examples 1 and 2 As the organic polymer flocculant, cationic Ni-2 was used in Comparative Example 1, and anionic A-1 was used in Comparative Example 2, and the other conditions were exactly the same as in Example 1. When the test was conducted, as shown in Table 2, the dehydrated cakes of both comparative examples were lumpy and had a high cake moisture content, and exhibited significantly worse performance than Example 1.
比較例3及び4
pH81M値を4.0及び9、Oとし、比較例4におい
てp)IvA整剤として硫酸を用いたこと以外はそれぞ
れ実施例1と全く同様にして脱水試験を行なった。いず
れの場合もフロックの粒径が小さく、比較例3の場合は
脱水ができたもののケーキ含水率が高く、又比較例4の
場合は脱水不良であった。Comparative Examples 3 and 4 A dehydration test was conducted in exactly the same manner as in Example 1, except that the pH81M values were set to 4.0, 9, and 0, and sulfuric acid was used as the p)IvA stabilizer in Comparative Example 4. In all cases, the particle size of the flocs was small; in Comparative Example 3, although dehydration was possible, the moisture content of the cake was high; and in Comparative Example 4, dehydration was insufficient.
実施例3及び4
pH;5,1、SS;2,2%、VTS;72,8%、
M−アルカリ度;415■/!なる性状の下水混合生汚
泥に対して、第3表に示す種類と量の無機゛凝゛集剤を
添加して約20秒間攪拌後、水酸化ナトリウム液を添加
してpHをそれぞれ6.0に調整した。pH調整開始か
ら約10分後に両性高分子凝集剤R−1を各々1.0%
ずつ添加してフロックを生成させ、フィルタープレスに
よる脱水試験を行なりた。その結果を第3表に示すが、
フロック粒径は良好であり、従来高分子凝集剤系では適
用が困難とされていたフィルタープレス脱水法が適用で
き、ケーキのF有刺離性、ケーキ含水率共に良好であっ
た。Examples 3 and 4 pH; 5,1, SS; 2,2%, VTS; 72,8%,
M-alkalinity; 415■/! To the sewage mixed raw sludge with the following properties, inorganic flocculants of the type and amount shown in Table 3 were added, and after stirring for about 20 seconds, sodium hydroxide solution was added to adjust the pH to 6.0. Adjusted to. Approximately 10 minutes after the start of pH adjustment, add 1.0% of each amphoteric polymer flocculant R-1.
A floc was generated by adding the flocs, and a dehydration test using a filter press was conducted. The results are shown in Table 3.
The floc particle size was good, the filter press dehydration method, which was conventionally considered difficult to apply using a polymer flocculant system, could be applied, and both the F prickly releasability of the cake and the cake moisture content were good.
比較例5
実施例3の汚泥に対し、実施例3と同様にして無機凝集
剤を添加したところpH値は4.0になった。Comparative Example 5 When an inorganic flocculant was added to the sludge of Example 3 in the same manner as in Example 3, the pH value became 4.0.
そこでpH調整を行なわないまま実施例3と同様にして
高分子凝集剤を添加してフロックを生成させたところ凝
集状態が悪く、フィルタープレスでhi脱水ができなか
った。Therefore, when a polymer flocculant was added to form flocs in the same manner as in Example 3 without adjusting the pH, the flocs were in poor condition and hi dehydration could not be performed using a filter press.
実施例5及び6
pH;5,5、SS;2,1%、VTS;78,1%、
M−アルカリ度”、750m9/11なる性状の下水混
合生汚泥に対し、実施例3と同様にして第3表の条件で
無機凝集剤の添加、pH調整、有機高分子凝集剤の添加
を行ない、ベルトプレスによる脱水試験を行なったとこ
ろ良好な結果が得られた。Examples 5 and 6 pH; 5,5, SS; 2,1%, VTS; 78,1%,
To sewage mixed raw sludge with properties of "M-alkalinity" and 750m9/11, an inorganic flocculant was added, the pH was adjusted, and an organic polymer flocculant was added under the conditions shown in Table 3 in the same manner as in Example 3. A dehydration test using a belt press gave good results.
比較例6〜8
比較例7においてpH調整剤として硫酸を用いたことを
除き、実施例5と同様にして、実施例5と同様の汚泥に
対し、第3表の条件で脱水試験を行なりた。Comparative Examples 6 to 8 A dehydration test was conducted on the same sludge as in Example 5 under the conditions shown in Table 3 in the same manner as in Example 5 except that sulfuric acid was used as the pH adjuster in Comparative Example 7. Ta.
比較例6のカチオン性有機高分子凝集剤を用いた場合は
フロック粒径が小さすぎて脱水ができなかった。When the cationic organic polymer flocculant of Comparative Example 6 was used, the floc particle size was too small to allow dehydration.
比較例7のpH調整値が低い場合もフロック径が小さく
脱水状態が不良であった。Even when the pH adjustment value of Comparative Example 7 was low, the floc diameter was small and the dehydration state was poor.
比較例8のpH調整値が高い場合は脱水ができたものの
ケーキ含水率が74.0%という高い値を示した。When the pH adjustment value of Comparative Example 8 was high, although dehydration was possible, the cake moisture content showed a high value of 74.0%.
実施例7及び8
pH;6.8、SS;1.8%、v’rs;6B、1%
、M−アルカリ度;3500■/lなる性状の下水消化
汚泥に対し、第3表の条件で無機凝集剤の添加、pH調
整、有機高分子凝集剤の添加ヲ行ない、ベルトプレスに
よる脱水試験を行なったところ、従来法に比較してケー
キ含水率を4〜6%程度低下させることができた。Examples 7 and 8 pH; 6.8, SS; 1.8%, v'rs; 6B, 1%
, M-Alkalinity: 3500 ■/l of sewage digested sludge was subjected to the addition of an inorganic flocculant, pH adjustment, addition of an organic polymer flocculant, and a dewatering test using a belt press under the conditions shown in Table 3. When carried out, it was possible to reduce the moisture content of the cake by about 4 to 6% compared to the conventional method.
比較例9〜12
比較例11においてpH調整剤として硫酸を用いたこと
を除き、実施例7と同様にして、実施例7と同様の汚泥
に対し、第3表の条件で脱水試験を行なりた。Comparative Examples 9 to 12 A dehydration test was conducted on the same sludge as in Example 7 under the conditions shown in Table 3 in the same manner as in Example 7 except that sulfuric acid was used as the pH adjuster in Comparative Example 11. Ta.
比較例9のカチオン性有機高分子凝集剤を用いた場合は
、フロック粒径が小さすぎて脱水ができなかった。When the cationic organic polymer flocculant of Comparative Example 9 was used, the floc particle size was too small to allow dehydration.
比較例10のカチオン性有機高分子凝集剤とアニオン性
有機高分子凝集剤を併用する場合はケーキの剥°離性が
悪く、ケーキ含水率も高かった。When the cationic organic polymer flocculant and anionic organic polymer flocculant of Comparative Example 10 were used together, the cake peelability was poor and the cake moisture content was high.
比較例11のpH調整値が低い場合は、フロック径が小
さく、ケーキのP有刺離性が悪く、比較例12の、pH
調整値が高い場合は、フロック粒径が小さく、ケーキ含
水率が高かった。When the pH adjustment value of Comparative Example 11 is low, the floc diameter is small and the P barbed releasability of the cake is poor, and the pH of Comparative Example 12 is low.
When the adjustment value was high, the floc particle size was small and the cake moisture content was high.
実施例の結果等から明らかなように、本発明の汚泥の脱
水方法は、以下に掲げる優れた効果を有している。As is clear from the results of Examples, the sludge dewatering method of the present invention has the following excellent effects.
(1)生成するフロック粒径が大きく、フロック強度が
優れているために、脱水ケーキのF有刺離性が優れてい
る。(1) Since the produced floc particle size is large and the floc strength is excellent, the F prickly releasability of the dehydrated cake is excellent.
(2)従来法と比較し、脱水ケーキの含水率がおよそ4
〜6%程度低いので汚泥焼却時の燃料費が著しく節約で
きる。(2) Compared to the conventional method, the moisture content of the dehydrated cake is approximately 4
Since it is about 6% lower, the fuel cost during sludge incineration can be significantly reduced.
(3)有機高分子凝集剤を用いた従来の脱水法では適用
不可能であったフィルタープレス型脱水機によっても良
好に脱水することができる。(3) Good dehydration can also be achieved using a filter press type dehydrator, which was not applicable to conventional dehydration methods using organic polymer flocculants.
Claims (2)
汚泥に対して両性有機高分子凝集剤を添加し、次いで脱
水することを特徴とする汚泥の脱水方法。(1) A method for dewatering sludge, which comprises adding an amphoteric organic polymer flocculant to organic sludge whose pH value after addition of the inorganic flocculant is 5 to 8, and then dewatering the organic sludge.
ボキシル基又はその塩を含有し、該両性有機高分子凝集
剤のカチオン当量値Cvが1.0〜4.0meq/g、
アニオン当量値Avが0.3〜2.0meq/g、Cv
/Avの比が1.5〜8.0であることを特徴とする特
許請求の範囲第1項記載の方法。(2) the amphoteric organic polymer flocculant contains a carboxyl group or a salt thereof as an anionic group, and the cation equivalent value Cv of the amphoteric organic polymer flocculant is 1.0 to 4.0 meq/g;
Anion equivalent value Av is 0.3 to 2.0 meq/g, Cv
2. The method according to claim 1, wherein the ratio of /Av is 1.5 to 8.0.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61305778A JPS63158200A (en) | 1986-12-22 | 1986-12-22 | Dehydration of sludge |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61305778A JPS63158200A (en) | 1986-12-22 | 1986-12-22 | Dehydration of sludge |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63158200A true JPS63158200A (en) | 1988-07-01 |
JPH0556199B2 JPH0556199B2 (en) | 1993-08-18 |
Family
ID=17949236
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61305778A Granted JPS63158200A (en) | 1986-12-22 | 1986-12-22 | Dehydration of sludge |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63158200A (en) |
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JPH02180700A (en) * | 1988-12-29 | 1990-07-13 | Kurita Water Ind Ltd | Dehydration of organic sludge |
JPH0321399A (en) * | 1989-06-19 | 1991-01-30 | Nippon Shokubai Kagaku Kogyo Co Ltd | Flocculation method of organic sludge |
JPH03207500A (en) * | 1990-01-09 | 1991-09-10 | Nippon Shokubai Kagaku Kogyo Co Ltd | Organic sludge dehydrating agent |
JPH04322800A (en) * | 1991-04-19 | 1992-11-12 | Kurita Water Ind Ltd | Method for dehydrating sludge |
JP2002045900A (en) * | 2000-08-08 | 2002-02-12 | Toagosei Co Ltd | Method for dewatering sludge |
KR100401982B1 (en) * | 1998-09-17 | 2004-01-24 | 주식회사 포스코 | The method of pressing sludge from steel making process |
US6872779B2 (en) | 1999-12-21 | 2005-03-29 | Toagosei Co., Ltd. | Polymeric flocculant and method of sludge dehydration |
US7141181B2 (en) | 2001-09-04 | 2006-11-28 | Toagosei Co., Ltd. | Composition comprising amphoteric polymeric flocculants |
JP2007253111A (en) * | 2006-03-24 | 2007-10-04 | Daiyanitorikkusu Kk | Water treatment process |
JP2012016658A (en) * | 2010-07-08 | 2012-01-26 | Hymo Corp | Sludge dehydrating agent and sludge dehydrating method |
JP2015000389A (en) * | 2013-06-18 | 2015-01-05 | 水ing株式会社 | Sludge treatment method and device |
JP2015003285A (en) * | 2013-06-19 | 2015-01-08 | 水ing株式会社 | Sludge treatment method and device |
KR20150067121A (en) | 2012-08-22 | 2015-06-17 | 엠티 아쿠아포리마 가부시키가이샤 | Polymer-coagulating agent and method for producing same, and method for dehydrating sludge using same |
WO2018168447A1 (en) | 2017-03-14 | 2018-09-20 | 栗田工業株式会社 | Sludge dehydrating agent and sludge dehydrating method |
KR20190124710A (en) | 2017-03-14 | 2019-11-05 | 쿠리타 고교 가부시키가이샤 | Sludge dehydrator and sludge dewatering method |
WO2019235345A1 (en) | 2018-06-06 | 2019-12-12 | 栗田工業株式会社 | Sludge dehydration agent and sludge dehydration method |
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JPH0556200B2 (en) * | 1989-06-19 | 1993-08-18 | Nippon Catalytic Chem Ind | |
JPH03207500A (en) * | 1990-01-09 | 1991-09-10 | Nippon Shokubai Kagaku Kogyo Co Ltd | Organic sludge dehydrating agent |
JPH04322800A (en) * | 1991-04-19 | 1992-11-12 | Kurita Water Ind Ltd | Method for dehydrating sludge |
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WO2007119479A1 (en) * | 2006-03-24 | 2007-10-25 | Dia-Nitrix Co., Ltd. | Water treatment method |
JP2007253111A (en) * | 2006-03-24 | 2007-10-04 | Daiyanitorikkusu Kk | Water treatment process |
US8614173B2 (en) | 2006-03-24 | 2013-12-24 | Dia-Nitrix Co., Ltd. | Water treatment method |
JP2012016658A (en) * | 2010-07-08 | 2012-01-26 | Hymo Corp | Sludge dehydrating agent and sludge dehydrating method |
KR20150067121A (en) | 2012-08-22 | 2015-06-17 | 엠티 아쿠아포리마 가부시키가이샤 | Polymer-coagulating agent and method for producing same, and method for dehydrating sludge using same |
JP2015000389A (en) * | 2013-06-18 | 2015-01-05 | 水ing株式会社 | Sludge treatment method and device |
JP2015003285A (en) * | 2013-06-19 | 2015-01-08 | 水ing株式会社 | Sludge treatment method and device |
WO2018168447A1 (en) | 2017-03-14 | 2018-09-20 | 栗田工業株式会社 | Sludge dehydrating agent and sludge dehydrating method |
KR20190124710A (en) | 2017-03-14 | 2019-11-05 | 쿠리타 고교 가부시키가이샤 | Sludge dehydrator and sludge dewatering method |
WO2019235345A1 (en) | 2018-06-06 | 2019-12-12 | 栗田工業株式会社 | Sludge dehydration agent and sludge dehydration method |
JP2019209287A (en) * | 2018-06-06 | 2019-12-12 | 栗田工業株式会社 | Sludge dehydrating agent, and sludge dewatering method |
KR20210018191A (en) | 2018-06-06 | 2021-02-17 | 쿠리타 고교 가부시키가이샤 | Sludge dehydration agent and sludge dehydration method |
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