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JPH0349606B2 - - Google Patents
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JPH0349606B2 - - Google Patents

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Publication number
JPH0349606B2
JPH0349606B2 JP61275601A JP27560186A JPH0349606B2 JP H0349606 B2 JPH0349606 B2 JP H0349606B2 JP 61275601 A JP61275601 A JP 61275601A JP 27560186 A JP27560186 A JP 27560186A JP H0349606 B2 JPH0349606 B2 JP H0349606B2
Authority
JP
Japan
Prior art keywords
sludge
lower alkyl
group
alkyl group
formula
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 - Lifetime
Application number
JP61275601A
Other languages
Japanese (ja)
Other versions
JPS63130108A (en
Inventor
Kenichi Kurokawa
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.)
DKS Co Ltd
Original Assignee
Dai Ichi Kogyo Seiyaku Co 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 Dai Ichi Kogyo Seiyaku Co Ltd filed Critical Dai Ichi Kogyo Seiyaku Co Ltd
Priority to JP61275601A priority Critical patent/JPS63130108A/en
Publication of JPS63130108A publication Critical patent/JPS63130108A/en
Publication of JPH0349606B2 publication Critical patent/JPH0349606B2/ja
Granted legal-status Critical Current

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  • Separation Of Suspended Particles By Flocculating Agents (AREA)
  • Treatment Of Sludge (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は、有機性汚泥の脱水法に関するもので
ある。さらに詳しくは無機塩類を含有する汚泥の
処理方法に係り、特に、その中に0.1重量%以上
の多量の無機塩類を含有する汚泥に有効な脱水法
に関するものである。 本発明の骨子とするところは、無機塩類を含有
する汚泥に、後述する一般式(1)、(2)、および(3)で
示される重合性ビニール単量体を一構成単位と
し、その割合が(1):(2):(3)=5〜45:5〜45:50
〜90(モル%)なる範囲の水溶性高分子重合体
(三元共重合体)を主成分とするカチオン系凝集
剤を添加することを特徴とする、無機塩類含有汚
泥の脱水法である。 水質保全のための排水規制の強化や下水、し尿
処理設備の普及にともなつて、産業廃水処理、下
水処理、し尿処理、その他で発生する各種汚泥の
脱水処理に各種のカチオン性高分子化合物が用い
られている。これらのカチオン性高分子化合物
は、従来の無機系の凝集剤に比較して低添加量で
優れた凝集性能を示し、且つ脱水後のケーキを焼
却した場合に発生する残滓が少ない等の長所を有
するので、現在では無機系凝集剤に代つて、汚泥
の処理に広く用いられてきている。 これらのカチオン性高分子化合物としては、ジ
メチルアミノエチルメタクリレートのホモポリマ
ー、ジメチルアミノエチルメタクリレートとアク
リルアミドとのコポリマー、ジメチルアミノエチ
ルメタクリレートの4級物のホモポリマーまたは
コポリマー、ポリアクリルアミドのマンニツヒ変
性物または、その4級化物、ポリビニルイミダゾ
リン、ジメチルジアリルアンモニウムクロライド
のホモポリマー等がある。 これらのカチオン性高分子化合物は、通常の汚
泥に対して極めて優れた凝集性能を示し、汚泥の
脱水処理に著しい効果を発揮している。 しかし、これらのカチオン性高分子化合物も本
発明の対象となる特殊な汚泥、すなわち、無機塩
類を多量に含む汚泥に対しては凝集性能が著しく
低下したり、凝集してもフロツク強度が弱いため
に壊れやすい等の現象が見られ、満足のいく脱水
効果が得られないという欠点があつた。また、高
塩類濃度の汚泥に対しては、ジメチルアミノエチ
ルメタクリレートのベンジルクロライド4級化物
のホモポリマーまたは、これとアクリルアミドと
のコポリマーがフロツクを生成するが、その脱水
効果は必ずしも満足できるものでなかつた。すな
わち、塩類濃度が様々に変化する高塩類濃度の汚
泥に対して安定した脱水が不可能であつた。 本発明は、以上のような従来技術の問題点を解
消すべく、鋭意研究の結果本発明に到達したもの
である。すなわち、本発明は、 下記一般式(1)、(2)、および(3)で表わされる重合性
ビニル単量体を一構成単位とし、その割合が(1):
(2):(3)=5〜45:5〜45:50〜90(モル%)なる
範囲で構成される水溶性高分子重合体(三元共重
合体)を主成分とするカチオン系凝集剤を汚泥に
添加することを特徴とする汚泥の脱水法を提供す
るものである。 一般式、 [但し、式(1)中R1は低級アルキル基、R2は低級
アルキレン基、R3、R4は低級アルキル基、R5は
ベンジル基、Xはアンモニウム窒素と塩を生成す
る陰性の基である] 一般式、 [但し、式(2)中R1は低級アルキル基、R2は低級
アルキレン基、R3、R4は低級アルキル基、R6は
低級アルキル基、Xはアンモニウム窒素と塩を生
成する陰性の基である] 一般式、 [但し、式(3)中R1は水素原子、または低級アル
キル基である] 本発明において対象となる汚泥は、無機塩類を
多量に含む汚泥であり、その代表的なものは、し
尿、またはし尿の消化脱離液を海水希釈し、活性
汚泥処理したときに生成する余剰汚泥、あるいは
この余剰汚泥と他の汚泥との混合汚泥がある。他
の汚泥としては、活性汚泥処理水の凝集沈澱汚
泥、消化汚泥等の汚泥であり、任意の割合で混合
することができる。 前記の海水希釈工程においては、消化脱離後の
約20倍量程度もの大量の海水を使用しており、こ
の希釈された消化脱離液を活性汚泥処理したとき
に生成する余剰汚泥は高濃度の無機塩類を含む。
しかし、この余剰汚泥が単独で脱水処理に供され
る場合は少なく、他の汚泥との混合による混合汚
泥として脱水処理に供される場合が多い。 余剰汚泥と他の汚泥との混合においては、その
混合が任意の割合で行なわれており、混合汚泥に
混入している無機塩類の濃度も様々である。 すなわち、余剰汚泥の割合が高い混合汚泥で
は、無機塩類の濃度も高いが、余剰汚泥の割合が
低い混合汚泥の場合は、無機塩類の濃度も低い、
ということが言える。このため、混合汚泥の脱水
を安定にしたものとするには、余剰汚泥単独での
脱水処理とは異なつた工夫が必要であり、混合汚
泥の性質、特に汚泥の電気伝導度に注目し、汚泥
中の無機塩類の濃度との関係把握に努めた。 この結果、無機塩類を含有する汚泥は、無機塩
類の濃度に応じて、電気伝導度の変化することが
明らかになつた。また、混合汚泥に占める余剰汚
泥の割合が変化すると、混合汚泥中に含まれる無
機塩類の濃度は、汚泥の全固形物[TS]から汚
泥の浮遊性固形物[SS]を差し引いた溶解性物
質濃度の変化としても捉えられる。このため汚泥
中の無機塩類の濃度および溶解性物質の濃度は、
電気伝導度の変化として捉えられる。したがつ
て、余剰汚泥の割合が変化する混合汚泥であつて
も、電気伝導度を測定することによつて、汚泥中
の無機塩類の濃度を瞬時に把握することができ
る。 混合汚泥の電気伝導度は通常2000μS/cm以上
であり、余剰汚泥の割合が高くなるに、従つて、
30000μS/cm以上となり、無機塩類の濃度が高い
ことが容易に確認できる。因に、溶解性物質濃度
が0.2%であれば、電気伝導度は約5000μS/cmで
あり、2%であれば、30000μS/cmと極めて高く
なる。このため、高塩類濃度の汚泥に有効である
とされているジメチルアミノエチルメタクリレー
トのベンジルクロライド4級化物のホモポリマー
または、これとアクリルアミドとのコポリマー
は、汚泥の電気伝導度がどの程度の値のときに、
有効であるかを検討した。この検討と同時に、通
常の汚泥に対して、優れた性能を示すジメチルア
ミノエチルメタクリレートのメチルクロライド4
級化物のホモポリマーまたは、これとアクリルア
ミドとのコポリマーについても検討した。 この結果、電気伝導度が2000μS/cm以下では、
ジメチルアミノエチルメタクリレートのメチルク
ロライド4級化物のホモポリマーまたは、これと
アクリルアミドとのコポリマーが優れた凝集性能
を示し、また、電気伝導度が30000μS/cm以上で
は、ジメチルアミノエチルメタクリレートのベン
ジルクロライド4級化物のホモポリマーまたは、
これとアクリルアミドとのコポリマーが優れた性
能を示した。しかし、電気伝導度が2000〜
30000μS/cmの間では、前記のいずれの種類のポ
リマーも単品での使用では優れた性能を発揮し得
なかつた。 本発明において使用できるカチオン性高分子重
合体としては、前記一般式(1)、(2)および(3)で表わ
される重合性ビニル単量体を構成単位とし、その
割合が(1):(2):(3)=5〜45:5〜45:50〜90(モ
ル%)なる範囲の水溶性高分子重合体(三元共重
合体)を主成分とするカチオン系凝集剤である。 このカチオン性高分子重合体の一構成単位であ
る一般式(1)で示される第4アンモニム塩は、一般
にジアルキルアミノアルキル(メタ)アクリレー
トをベンジルハライドで4級化することにより得
られ、これのホモポリマーまたは、これとアクリ
ルアミドとのコポリマーが高塩類濃度の汚泥に対
して比較的有効であることは、既に述べた通りで
ある。 また、一般式(2)で示される第4アンモニウム塩
は、一般にジアルキルアミノアルキル(メタ)ア
クリレートをメチルハライドで4級化することに
より得られ、これのホモポリマーまたは、これと
アクリルアミドとのコポリマーが通常の汚泥に対
して有効であることは良く知られている。 すなわち、一般式(1)で示される第4アンモニム
塩のホモポリマーまたは、これとアクリルアミド
とのコポリマーは、汚泥の電気伝導度が
30000μS/cmを越えれば、固液分離を行なうに充
分な大きさと強度を併せ持つたフロツクを形成
し、凝集汚泥の濾過脱水速度も早く、得られる脱
水ケーキ含水率が低い。また一般式(2)で示される
第4級アンモニム塩のホモポリマーまたは、これ
とアクリルアミドとのコポリマーは、汚泥の電気
伝導度が3000μS/cm未満であれば、固液分離を
行なうに充分な大きさと強度を併せ持つたフロツ
クを形成し、凝集汚泥の濾過脱水測度が早く、得
られる脱水ケーキ含水率が低い。しかし、汚泥の
電気伝導度が3000〜30000μS/cmであれば、前記
ポリマーのいずれも固液分離を行なうに充分な大
きさと強度を併せ持つたフロツクを形成せず、凝
集汚泥の濾過脱水速度も遅く、得られる脱水ケー
キ含水率が高い。 したがつて、汚泥の電気伝導度が3000〜
30000μS/cmの場合、一般式(1)で示される第4ア
ンモニム塩のホモポリマーまたは、これとアクリ
ルアミドとのコポリマー、あるいは一般式(2)で示
される第4アンモニム塩のホモポリマーまたは、
これとアクリルアミドとのコポリマーでは、優れ
た性能を発揮しない。 これに対して、前記一般式(1)、(2)および(3)で表
わされる重合性ビニル単量体を構成単位とし、そ
の割合が(1):(2):(3)=5〜45:5〜45:50〜90
(モル%)なる範囲の水溶性高分子重合体(三元
共重合体)は、固液分離を行なうに充分な大きさ
と強度を併せ持つたフロツクを形成し、凝集汚泥
の濾過脱水速度も早く、得られる脱水ケーキ含水
率が低く、優れた凝集性能を示す。 これらの検討結果は実施例および比較例によつ
て、具体的に説明するが、試験法は従来から汚泥
脱水試験に多用されているもので、処理場で用い
られている脱水機での効果と相関性の高いテスト
法であつて、実施例で説明した要領で行なつた。
しかし、各薬剤の添加率は、汚泥の性状[PH、
SS、VSS/SS、電気伝導度]によつて異なるの
で、実施例に限定されるものではなく、0.5〜10
重量%[対SS]、好ましくは1〜5重量%[対
SS]である。 なお、実施例および比較例における撹拌後のフ
ロツク径は4mm以上であるものが、固液分離を行
なうに望ましい大きさであるが、緻密な構造であ
ることが重要であり、大きければ良いというもの
ではない。また、10秒後の瀘液量は濾過脱水速度
やケーキ含水率の指標となるものであり、10秒後
の瀘液量が大であるとの濾過脱水速度が早く、ケ
ーキ含水率も低いといえる。 次に本発明を実施例により具体的に説明する。
[%、部は重量基準を示す] 実施例 1 し尿の消化脱離液を海水希釈し、活性汚泥処理
したときに生成した余剰汚泥と消化汚泥との混合
汚泥[PH6.6、電気伝導度20100μS/cm、SS;
11500mg/1、VSS/SS;83.1%]を300mlビー
カーに200ml秤り取り、これに第1表に示す各種
薬剤0.2%水溶液を第1表記載の所定量添加し、
撹拌機により180rpmで30秒間撹拌し、フロツク
を生成させた。フロツク径測定後、100メツシユ
のナイロン製濾布を敷いたブフナーロートにフロ
ツクを生成した汚泥を注ぎ、10秒後の瀘液量を測
定した、その後、濾過を継続して濾過完了後の汚
泥を10g採取し、濾布[ポリエステル朱子織]お
よびスポンジで挟み、1.5Kg/cm2の圧力で3分間
圧搾した後、汚泥のケーキ含水率を測定した。そ
の結果を第1表に記載した。 第1表により、実施例のものは比較例のものよ
りもフロツク径が大きく、濾過脱水速度が早く、
ケーキ含水率の低いことが確認できる。 実施例 2 し尿の消化脱離液を海水希釈し、活性汚泥処理
したときに生成した余剰汚泥と消化汚泥との混合
汚泥[PH6.8、電気伝導度28000μS/cm、SS;
12100mg/1、VSS/SS;82.9%]を300mlビー
カーに200ml秤り取り、これに第2表に示す各種
薬剤0.2%水溶液を第2表記載の所定量添加し、
撹拌機により180rpmで30秒間撹拌し、フロツク
を生成させた。フロツク径測定後、100メツシユ
のナイロン製濾布を敷いたブフナーロートにフロ
ツクを生成した汚泥を注ぎ、10秒後の瀘液量を測
定した、その後、濾過を継続して濾過完了後の汚
泥を10g採取し、濾布[ポリエステル朱子織]お
よびスポンジで挟み、1.5Kg/cm2の圧力で3分間
搾した後、汚泥のケーキ含水率を測定した。その
結果を第2表に記載した。 第2表により、実施例のものは比較例のものよ
りもフロツク径が大きく、濾過脱水速度が早く、
ケーキ含水率の低いことが確認できる。 実施例 3 し尿を活性汚泥処理の変法である高負荷生物酸
化方法で処理したときに生成した余剰汚泥と無機
凝集剤で凝集沈澱した汚泥との混合汚泥[PH7.1、
電気伝導度10500μS/cm、SS;10800mg/1、
VSS/SS;78.8%]を300mlビーカーに200ml秤
り取り、これに第3表に示す各種薬剤0.2%水溶
液を第3表記載の所定量添加し、撹拌機により
180rpmで30秒間撹拌し、フロツクを生成させた。
フロツク径測定後、100メツシユのナイロン製濾
布を敷いたブフナーロートにフロツクを生成した
汚泥を注ぎ、10秒後の瀘液量を測定した、その
後、濾過を継続して濾過完了後の汚泥を10g採取
し、濾布[ポリエステル朱子織]およびスポンジ
で挟み、1.5Kg/cm2の圧力で3分間圧搾した後、
汚泥のケーキ含水率を測定した。その結果を第3
表に記載した。 第3表により、実施例のものは比較例のものよ
りもフロツク径が大きく、濾過脱水速度が早く、
ケーキ含水率の低いことが確認できる。
The present invention relates to a method for dewatering organic sludge. More specifically, the present invention relates to a method for treating sludge containing inorganic salts, and particularly to a dewatering method effective for sludge containing a large amount of inorganic salts of 0.1% by weight or more. The gist of the present invention is to add polymerizable vinyl monomers represented by general formulas (1), (2), and (3) below to sludge containing inorganic salts as one structural unit, and to is (1):(2):(3)=5~45:5~45:50
This is a dewatering method for sludge containing inorganic salts, which is characterized by adding a cationic flocculant whose main component is a water-soluble polymer (terpolymer) in a range of 90 (mol %). With the tightening of wastewater regulations to preserve water quality and the spread of sewage and human waste treatment equipment, various cationic polymer compounds are being used to dehydrate various types of sludge generated in industrial wastewater treatment, sewage treatment, human waste treatment, and other processes. It is used. These cationic polymer compounds exhibit superior flocculating performance at lower amounts than conventional inorganic flocculants, and have other advantages such as less residue generated when the cake is incinerated after dehydration. Because of this, it is now widely used in the treatment of sludge in place of inorganic flocculants. These cationic polymer compounds include homopolymers of dimethylaminoethyl methacrylate, copolymers of dimethylaminoethyl methacrylate and acrylamide, homopolymers or copolymers of quaternary dimethylaminoethyl methacrylate, Mannitz modified polyacrylamide, or There are quaternized products thereof, polyvinylimidazoline, homopolymers of dimethyldiallylammonium chloride, and the like. These cationic polymer compounds exhibit extremely excellent flocculation performance against ordinary sludge, and are extremely effective in dewatering sludge. However, these cationic polymer compounds also have a markedly reduced flocculation performance for the special sludge that is the subject of the present invention, that is, sludge containing a large amount of inorganic salts, and even if they flocculate, the floc strength is weak. However, there were phenomena such as easy breakage, and the disadvantage was that a satisfactory dehydration effect could not be obtained. In addition, for sludge with high salt concentration, a homopolymer of benzyl chloride quaternized dimethylaminoethyl methacrylate or a copolymer of this with acrylamide produces flocs, but the dewatering effect is not always satisfactory. Ta. That is, it has been impossible to perform stable dewatering of sludge with a high salt concentration that varies in salt concentration. The present invention was achieved as a result of intensive research in order to solve the problems of the prior art as described above. That is, the present invention uses polymerizable vinyl monomers represented by the following general formulas (1), (2), and (3) as one structural unit, and the proportion thereof is (1):
(2):(3)=5-45:5-45:50-90 (mol%) Cationic aggregation mainly composed of a water-soluble polymer (terpolymer) The present invention provides a sludge dewatering method characterized by adding an agent to sludge. general formula, [However, in formula (1), R1 is a lower alkyl group, R2 is a lower alkylene group, R3 and R4 are lower alkyl groups, R5 is a benzyl group, and X is a negative group that forms a salt with ammonium nitrogen] General formula , [However, in formula (2), R1 is a lower alkyl group, R2 is a lower alkylene group, R3 and R4 are a lower alkyl group, R6 is a lower alkyl group, and X is a negative group that forms a salt with ammonium nitrogen.] General formula, [However, R1 in formula (3) is a hydrogen atom or a lower alkyl group] The sludge that is the object of the present invention is a sludge that contains a large amount of inorganic salts, and a typical example thereof is human waste or human waste. There is surplus sludge produced when the digested and desorbed fluid is diluted with seawater and treated with activated sludge, or a mixed sludge of this surplus sludge and other sludge. Other sludges include sludges such as coagulated sedimentation sludge of activated sludge treated water and digested sludge, which can be mixed in any proportion. In the seawater dilution process mentioned above, a large amount of seawater is used, about 20 times the amount after digestion and desorption, and the surplus sludge produced when this diluted digestion and desorption liquid is treated with activated sludge has a high concentration. Contains inorganic salts.
However, this surplus sludge is rarely subjected to dewatering treatment alone, and is often subjected to dewatering treatment as mixed sludge by mixing it with other sludge. When mixing surplus sludge with other sludge, the mixing is performed at an arbitrary ratio, and the concentration of inorganic salts mixed in the mixed sludge also varies. In other words, mixed sludge with a high proportion of surplus sludge has a high concentration of inorganic salts, but mixed sludge with a low proportion of surplus sludge has a low concentration of inorganic salts.
That can be said. Therefore, in order to make the dewatering of mixed sludge stable, it is necessary to take a different approach from dewatering treatment of surplus sludge alone. We endeavored to understand the relationship with the concentration of inorganic salts in the water. The results revealed that the electrical conductivity of sludge containing inorganic salts changes depending on the concentration of inorganic salts. In addition, when the proportion of surplus sludge in the mixed sludge changes, the concentration of inorganic salts contained in the mixed sludge is calculated by subtracting the suspended solids [SS] from the total solids [TS] of the sludge. It can also be interpreted as a change in concentration. Therefore, the concentration of inorganic salts and the concentration of soluble substances in sludge are
This can be interpreted as a change in electrical conductivity. Therefore, even if the mixed sludge has a varying proportion of surplus sludge, the concentration of inorganic salts in the sludge can be instantly determined by measuring the electrical conductivity. The electrical conductivity of mixed sludge is usually more than 2000μS/cm, and as the proportion of surplus sludge increases,
It is more than 30000μS/cm, and it can be easily confirmed that the concentration of inorganic salts is high. Incidentally, if the soluble substance concentration is 0.2%, the electrical conductivity is about 5000 μS/cm, and if it is 2%, it is extremely high at 30000 μS/cm. For this reason, the homopolymer of benzyl chloride quaternized dimethylaminoethyl methacrylate, which is said to be effective for sludge with high salt concentration, or the copolymer of this and acrylamide, has a high electrical conductivity of sludge. sometimes,
We examined whether it is effective. At the same time as this study, methyl chloride 4 of dimethylaminoethyl methacrylate, which shows excellent performance against ordinary sludge, was developed.
We also investigated homopolymers of these compounds and copolymers of them with acrylamide. As a result, when the electrical conductivity is less than 2000μS/cm,
A homopolymer of methyl chloride quaternary of dimethylaminoethyl methacrylate or a copolymer of this with acrylamide exhibits excellent flocculation performance. homopolymers of compounds or
A copolymer of this with acrylamide showed excellent performance. However, the electrical conductivity is 2000~
Between 30,000 μS/cm, none of the above-mentioned types of polymers could exhibit excellent performance when used alone. The cationic polymer that can be used in the present invention has polymerizable vinyl monomers represented by the general formulas (1), (2), and (3) as structural units, and the ratio thereof is (1):( It is a cationic flocculant whose main component is a water-soluble polymer (terpolymer) in the range of 2):(3)=5 to 45:5 to 45:50 to 90 (mol%). The quaternary ammonium salt represented by the general formula (1), which is a constituent unit of this cationic polymer, is generally obtained by quaternizing dialkylaminoalkyl (meth)acrylate with benzyl halide; As already mentioned, homopolymers or copolymers of homopolymers and acrylamide are relatively effective against sludge with high salt concentrations. In addition, the quaternary ammonium salt represented by the general formula (2) is generally obtained by quaternizing dialkylaminoalkyl (meth)acrylate with methyl halide, and a homopolymer thereof or a copolymer of this and acrylamide is used. It is well known that it is effective against ordinary sludge. In other words, the quaternary ammonium salt homopolymer represented by the general formula (1) or the copolymer of this with acrylamide has a high electrical conductivity of sludge.
If it exceeds 30,000 μS/cm, flocs with sufficient size and strength for solid-liquid separation will be formed, the rate of filtration and dewatering of flocculated sludge will be high, and the water content of the resulting dehydrated cake will be low. In addition, the quaternary ammonium salt homopolymer represented by general formula (2) or the copolymer of this with acrylamide has a sufficient size for solid-liquid separation if the electrical conductivity of the sludge is less than 3000 μS/cm. It forms flocs that have both strength and strength, allows rapid filtration and dehydration of flocculated sludge, and results in a low moisture content of the resulting dehydrated cake. However, if the electrical conductivity of the sludge is 3,000 to 30,000 μS/cm, none of the above polymers will form flocs with sufficient size and strength for solid-liquid separation, and the rate of filtration and dewatering of flocculated sludge will be slow. , the resulting dehydrated cake has a high moisture content. Therefore, the electrical conductivity of sludge is 3000~
In the case of 30000 μS/cm, a homopolymer of a quaternary ammonium salt represented by the general formula (1), a copolymer of this with acrylamide, a homopolymer of a quaternary ammonium salt represented by the general formula (2), or
Copolymers of this and acrylamide do not exhibit excellent performance. On the other hand, the polymerizable vinyl monomers represented by the general formulas (1), (2), and (3) are used as structural units, and the ratio is (1):(2):(3)=5 to 45:5~45:50~90
The water-soluble polymer (terpolymer) in the range of (mol%) forms flocs with sufficient size and strength for solid-liquid separation, and the rate of filtration and dewatering of coagulated sludge is fast. The resulting dehydrated cake has a low moisture content and exhibits excellent flocculation performance. The results of these studies will be explained in detail using examples and comparative examples, but the test method is one that has been widely used in sludge dewatering tests, and the effectiveness and effectiveness of dewatering machines used in treatment plants. This is a highly correlated test method and was conducted in the same manner as described in the Examples.
However, the addition rate of each chemical depends on the properties of the sludge [PH,
SS, VSS/SS, electrical conductivity], so it is not limited to the examples, and is 0.5 to 10
% by weight [vs. SS], preferably 1 to 5% by weight [vs.
SS]. In addition, in Examples and Comparative Examples, the floc diameter after stirring is 4 mm or more, which is a desirable size for solid-liquid separation, but it is important to have a dense structure, and the larger the better. isn't it. In addition, the amount of filtrate after 10 seconds is an indicator of the filtration dehydration rate and cake moisture content, and the larger the filtrate amount after 10 seconds, the faster the filtration and dehydration rate, and the lower the cake moisture content. I can say that. Next, the present invention will be specifically explained using examples.
[% and parts indicate weight basis] Example 1 Mixed sludge of surplus sludge and digested sludge produced when the digested and desorbed human waste was diluted with seawater and treated with activated sludge [PH6.6, electrical conductivity 20100 μS] /cm, SS;
11500mg/1, VSS/SS; 83.1%] was weighed out in a 300ml beaker, and 0.2% aqueous solutions of various drugs shown in Table 1 were added in the prescribed amounts shown in Table 1.
The mixture was stirred with a stirrer at 180 rpm for 30 seconds to form a floc. After measuring the floc diameter, the floc-forming sludge was poured into a Buchner funnel lined with a 100-mesh nylon filter cloth, and the amount of filtrate was measured after 10 seconds.Then, filtration was continued and the sludge was collected after filtration. 10g of the sludge was collected, sandwiched between a filter cloth [polyester satin weave] and a sponge, and squeezed for 3 minutes at a pressure of 1.5 kg/cm 2 , and then the moisture content of the sludge cake was measured. The results are listed in Table 1. According to Table 1, the floc diameter of the example is larger than that of the comparative example, and the filtration and dewatering speed is faster.
It can be confirmed that the cake moisture content is low. Example 2 Mixed sludge of surplus sludge and digested sludge produced when the digested and desorbed liquid of human waste was diluted with seawater and treated with activated sludge [PH6.8, electrical conductivity 28000μS/cm, SS;
12100mg/1, VSS/SS; 82.9%] was weighed out in a 300ml beaker, and 0.2% aqueous solutions of various drugs shown in Table 2 were added in the prescribed amounts shown in Table 2.
The mixture was stirred with a stirrer at 180 rpm for 30 seconds to form a floc. After measuring the floc diameter, the floc-forming sludge was poured into a Buchner funnel lined with a 100-mesh nylon filter cloth, and the amount of filtrate was measured after 10 seconds.Then, filtration was continued and the sludge was collected after filtration. 10g of the sludge was collected, sandwiched between a filter cloth [polyester satin weave] and a sponge, and squeezed for 3 minutes at a pressure of 1.5 kg/cm 2 , and then the moisture content of the sludge cake was measured. The results are listed in Table 2. According to Table 2, the floc diameter of the example is larger than that of the comparative example, and the filtration and dewatering speed is faster.
It can be confirmed that the cake moisture content is low. Example 3 Mixed sludge [PH7.1,
Electrical conductivity 10500μS/cm, SS; 10800mg/1,
Weigh out 200 ml of VSS/SS; 78.8%] into a 300 ml beaker, add the prescribed amounts of 0.2% aqueous solutions of various chemicals listed in Table 3, and use a stirrer to
Stir at 180 rpm for 30 seconds to form a floc.
After measuring the floc diameter, the floc-forming sludge was poured into a Buchner funnel lined with a 100-mesh nylon filter cloth, and the amount of filtrate was measured after 10 seconds.Then, filtration was continued and the sludge was collected after filtration. 10g was collected, sandwiched between a filter cloth [polyester satin weave] and a sponge, and squeezed for 3 minutes at a pressure of 1.5Kg/cm 2 .
The cake moisture content of the sludge was measured. The result is the third
It is listed in the table. According to Table 3, the floc diameter of the example is larger than that of the comparative example, and the filtration and dewatering speed is faster.
It can be confirmed that the cake moisture content is low.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 下記一般式(1)、(2)および(3)で表わされる重合
性ビニル単量体を一構成単位とし、その割合が
(1):(2):(3)=5〜45:5〜45:50〜90[モル%]
なる範囲で構成される水溶性高分子重合体(三元
共重合体)を主成分とするカチオン系凝集剤を汚
泥に添加することを特徴とする汚泥の脱水法。 一般式、 [但し、式(1)中R1は低級アルキル基、R2は低級
アルキレン基、R3、R4は低級アルキル基、R5は
ベンジル基、Xはアンモニウム窒素と塩を生成す
る陰性の基である] 一般式、 [但し、式(2)中R1は低級アルキル基、R2は低級
アルキレン基、R3、R4は低級アルキル基、R6は
低級アルキル基、Xはアンモニウム窒素と塩を生
成する陰性の基である] 一般式、 [但し、式(3)中R1は水素原子、または低級アル
キル基である]
[Claims] 1. Polymerizable vinyl monomers represented by the following general formulas (1), (2) and (3) are considered as one structural unit, and the proportion thereof is
(1):(2):(3)=5-45:5-45:50-90 [mol%]
A sludge dewatering method characterized by adding to sludge a cationic flocculant whose main component is a water-soluble polymer (terpolymer) consisting of the following: general formula, [However, in formula (1), R1 is a lower alkyl group, R2 is a lower alkylene group, R3 and R4 are lower alkyl groups, R5 is a benzyl group, and X is a negative group that forms a salt with ammonium nitrogen] General formula , [However, in formula (2), R1 is a lower alkyl group, R2 is a lower alkylene group, R3 and R4 are a lower alkyl group, R6 is a lower alkyl group, and X is a negative group that forms a salt with ammonium nitrogen.] General formula, [However, R1 in formula (3) is a hydrogen atom or a lower alkyl group]
JP61275601A 1986-11-19 1986-11-19 Method for dehydrating sludge Granted JPS63130108A (en)

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JP61275601A JPS63130108A (en) 1986-11-19 1986-11-19 Method for dehydrating sludge

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JP61275601A JPS63130108A (en) 1986-11-19 1986-11-19 Method for dehydrating sludge

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JPS63130108A JPS63130108A (en) 1988-06-02
JPH0349606B2 true JPH0349606B2 (en) 1991-07-30

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JP4498762B2 (en) * 2004-01-29 2010-07-07 友岡化研株式会社 Organic coagulants and polymer flocculants
JP5732818B2 (en) * 2010-11-05 2015-06-10 栗田工業株式会社 Sludge dewatering agent and sludge dewatering method

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JPS5559806A (en) * 1978-10-27 1980-05-06 Sanyo Chem Ind Ltd Cationic high molecular flocculant and flocculating method
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