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JPS6134873B2 - - Google Patents
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JPS6134873B2 - - Google Patents

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Publication number
JPS6134873B2
JPS6134873B2 JP55065079A JP6507980A JPS6134873B2 JP S6134873 B2 JPS6134873 B2 JP S6134873B2 JP 55065079 A JP55065079 A JP 55065079A JP 6507980 A JP6507980 A JP 6507980A JP S6134873 B2 JPS6134873 B2 JP S6134873B2
Authority
JP
Japan
Prior art keywords
waste
water
days
solidification
fine powder
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
JP55065079A
Other languages
Japanese (ja)
Other versions
JPS56161880A (en
Inventor
Chiaki Igarashi
Yoshe Aoyanagi
Noritsuna Saito
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.)
Ebara Corp
Original Assignee
Ebara Infilco 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 Ebara Infilco Co Ltd filed Critical Ebara Infilco Co Ltd
Priority to JP6507980A priority Critical patent/JPS56161880A/en
Publication of JPS56161880A publication Critical patent/JPS56161880A/en
Publication of JPS6134873B2 publication Critical patent/JPS6134873B2/ja
Granted legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/30Fuel from waste, e.g. synthetic alcohol or diesel

Landscapes

  • Processing Of Solid Wastes (AREA)

Description

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

本発明は、都市ゴミ、汚泥、ヘドロ等の焼却工
程から排出される焼却灰、ならびに各種ガス処理
工程から生じるダスト等の微粉状廃棄物の固化処
理方法に関するものである。 一般に、これら微粉状廃棄物の処理又は処分方
法としては、直接埋立、海洋投棄が主流であつた
が、微粉体であるために取扱いが厄介であり、運
搬途中や埋立地において飛散、流出が著しいな
ど、改善されなければならない点があつた。 また、これら微粉状廃棄物の取扱いを容易に
し、重金属等の溶出を防止するために、各種の固
化技術が提案されているが、この従来の固化技術
としてはセメントやアスフアルト等の固化剤を添
加する方法や、加熱溶融したのち放冷固化する方
法(溶融法)などがあつた。これらのうち、固化
剤を添加する方法は、有害物質の封じ込めや埋立
地の土質の改善等に効果があるが、固化剤の価格
が高く、日々排出される前記微粉状廃棄物の全量
を固化することは困難である。一方、前記溶融法
は、廃棄物の体積が著しく減少し、粒状若しくは
塊状になるために取扱いが容易で、重金属等の有
害物質を封じ込めることもでき、すぐれた方法で
あるが、廃棄物を高温に加熱保持する必要があ
り、エネルギを大量に使用する点で難がある。こ
のように、従来の廃棄物固化技術には解決しなけ
ればならない問題が数多くあり、省資源、省エネ
ルギの観点から、新しい技術を開発する必要にせ
まられているのが現状である。 本発明は、かかる現状に対して、微粉状廃棄物
を、低コスト、省エネルギ的に固化して取扱いを
容易にし、再利用の道を拓くことができる有効な
処理方法を提供することを目的とするものであ
る。 本発明は、微粉状廃棄物をカルシウム成分の存
在下で、固化促進剤、環元剤の少なくとも一方を
必要に応じ添加混合して成型した後、大気圧下
で、50℃以上の水又は温度50℃以上の水蒸気中
に、3日間以上放置、養生することを特徴とする
ものである。 本発明は、微粉状廃棄物の固化処理に、養生条
件が重要であることを明らかにしたことにより完
成されたものである。即ち、本発明者等は数多く
の実験結果から、養生雰囲気としては、乾燥空気
より水蒸気あるいは水が良く温度は50℃以上が、
また、養生時間は3日間以上が好ましいことを確
認したのである。 本発明においては、カルシウム成分の存在が必
要不可欠の条件であるが、前記微粉状廃棄物中に
カルシウム成分が十分含有されている場合はカル
シウム成分を添加しなくてよいが、不十分な場合
にはカルシウム成分を予め添加して、混合物中の
カルシウム分を10重量%(生石灰換算、以下
「%」はすべて重量基準で表示してある)以上と
するとよい。また、添加するカルシウム成分の形
態としては、炭酸カルシウム、生石灰、硫酸カル
シウム、塩化カルシウム、消石灰等を単独又は組
合わせて添加混合するが、このうち消石灰が最適
であり、場合によつてはカルシウム成分を用いて
脱水した各種汚泥を焼却して得られる残渣を用い
ることもできる。 また、カルシウム成分が十分でも固化しにくい
場合には必要に応じて固化促進剤としてけいそう
土、けい華、けい酸白土、けい石、石英、けい酸
ガラス、水ガラス、砂等のけい酸質物質、カオリ
ナイト、ベントナイト、パーライト、ゼオライ
ト、ハロサイト等の粘土類、水酸化アルミニウ
ム、酸化アルミニウム等のアルミニウム化合物、
または上記物質を含むフライアツシユ、赤泥焼却
灰等の廃棄物を単独あるいは、複数組合わせて適
当量(例えば1〜30%、好ましくは10〜30%)添
加して処理するのが効果的である。 さらに、重金属として6価クロムを大量に含む
微粉状廃棄物を処理するにあたつては、あらかじ
め還元剤を添加しておくことも有効である。この
場合還元剤としては、2価鉄イオンの塩、亜硫酸
又は亜硫酸塩、石英、カーボンブラツク、コーク
スのもえ殻、リグニン等の有機炭素類、マグネシ
ウム、カルシウム、亜鉛等の金属あるいはこれら
を含む廃棄物などを単独あるいは複数選んで用い
るとよい。また、その添加量は、場合によつて異
なるが一般には0.5〜20%程度が好ましい。 このように化学組成を調整された微粉状廃棄物
は、微粉同士の接触点数を増加させるために成型
されるが、この成型方法は、加圧、転動、押し出
し等従来の技術をそのまま利用できる。成型方法
によつては必ずしもバインダを必要としない場合
もあるが、本発明においてはバインダとして水を
用いると固化反応にも好都合となる。この場合、
添加する水量は、各々の成型方法に最適な量とす
るが、一般には転動造粒の場合、乾燥物の20〜30
%であり、圧縮成型の場合は5〜15%程度が効果
的である。 かくして成型された廃棄物は、大気圧下で、50
℃以上の水中又は50℃以上の水蒸気中に3日以上
放置されて固化する。最適な養生温度、養生時間
は廃棄物の組成等によつて大きく異なるが、概ね
それぞれ60〜80℃、3〜28日間位が経済的にも好
ましい条件である。なお、本発明においては水中
養生と水蒸気中養生を併せて行つてもよい。 養生工程において生じる反応の機構に関して
は、反応生成物の同定や定量が難しいために必ず
しも明らかではないが、カルシウムシリケート水
和物、あるいはカルシウムアルミネート水和物の
生成と、これによる微粉体相互の結合に基づく強
度の発現が進行するものと考えられる。 以上述べたように、本発明に微粉状廃棄物をカ
ルシウム成分の存在下で固化促進剤、還元剤の少
なくとも一方を必要に応じ添加混合して成型した
後、圧力が大気圧で、50℃以上の水中又は50℃以
上の水蒸気中に3日間以上放置することにより、
容易に強固な固化物を得ることができ、粉体のハ
ンドリンク性を改善し、埋立地面積を大幅に低減
させることができ、場合によつては路盤材や骨材
として再利用を可能にし、事後処理の簡便化がで
き、廃棄物の焼却処理工程から生じる熱や水蒸気
を加温に用いればより省エネルギ的な固化方法と
なり公害防止上極めて有用なる効果を有するもの
で、従来の諸問題も適確に排除し、しかも処理コ
ストも安価で経済的に処分できるなどの利益があ
る。 次に本発明の実施例を示す。 実施例 1 某下水処理場で発生した汚泥に消石灰と塩化第
二鉄を添加して脱水し、乾燥後焼却して得た焼却
灰の組成は次の通りであつた。
The present invention relates to a method for solidifying incinerated ash discharged from the incineration process of municipal garbage, sludge, sludge, etc., and fine powder waste such as dust generated from various gas processing processes. In general, direct landfilling and ocean dumping have been the mainstream methods for treating or disposing of these fine powder wastes, but since they are fine powders, they are difficult to handle, and they are prone to scattering and spilling during transportation and at landfill sites. There were some points that needed to be improved. In addition, various solidification technologies have been proposed to facilitate the handling of these fine powder wastes and prevent the elution of heavy metals, etc., but conventional solidification techniques involve adding solidification agents such as cement or asphalt. There were methods such as heating, melting, and then cooling and solidifying (melting method). Among these methods, the method of adding a solidifying agent is effective in containing harmful substances and improving the soil quality of a landfill, but the cost of the solidifying agent is high, and the method of adding a solidifying agent is effective in containing the hazardous substances and improving the soil quality of the landfill. It is difficult to do so. On the other hand, the melting method is an excellent method because the volume of the waste is significantly reduced and the waste becomes granular or lumpy, so it is easy to handle and can contain hazardous substances such as heavy metals. The problem is that it requires a large amount of energy to be heated. As described above, there are many problems that need to be solved with conventional waste solidification technologies, and the current situation is that there is an urgent need to develop new technologies from the viewpoint of resource and energy conservation. In view of the current situation, the present invention aims to provide an effective treatment method that can solidify fine powder waste in a low-cost and energy-saving manner, making it easier to handle and paving the way for reuse. That is. The present invention involves molding fine powder waste in the presence of a calcium component by adding and mixing at least one of a solidification accelerator and a cyclic agent as necessary, and then molding the waste in water at a temperature of 50°C or higher or at a temperature of 50°C or higher under atmospheric pressure. It is characterized by being left and cured in steam at a temperature of 50°C or higher for 3 days or more. The present invention was completed by clarifying that curing conditions are important in the solidification treatment of finely powdered waste. In other words, the inventors have found from numerous experimental results that steam or water is better for the curing atmosphere than dry air at a temperature of 50°C or higher.
It was also confirmed that a curing time of 3 days or more is preferable. In the present invention, the presence of a calcium component is an essential condition. If the fine powder waste contains a sufficient amount of calcium component, it is not necessary to add the calcium component, but if it is insufficient, It is preferable to add a calcium component in advance so that the calcium content in the mixture is 10% by weight or more (in terms of quicklime, hereinafter "%" is expressed on a weight basis) or more. In addition, as for the form of the calcium component to be added, calcium carbonate, quicklime, calcium sulfate, calcium chloride, slaked lime, etc. may be added singly or in combination, but among these, slaked lime is most suitable; It is also possible to use the residue obtained by incinerating various types of sludge that have been dehydrated using. In addition, if the calcium content is sufficient but hard to solidify, silicic acid materials such as diatomaceous earth, silica, silicate clay, silica stone, quartz, silicate glass, water glass, and sand can be used as a solidification accelerator as necessary. substances, clays such as kaolinite, bentonite, pearlite, zeolite, hallosite, aluminum compounds such as aluminum hydroxide and aluminum oxide,
Alternatively, it is effective to add an appropriate amount (for example, 1 to 30%, preferably 10 to 30%) of waste such as fly ash, red mud incineration ash, etc. containing the above substances singly or in combination. . Furthermore, when treating fine powder waste containing a large amount of hexavalent chromium as a heavy metal, it is also effective to add a reducing agent in advance. In this case, reducing agents include salts of divalent iron ions, sulfites or sulfites, quartz, carbon black, coke husks, organic carbons such as lignin, metals such as magnesium, calcium, zinc, etc., or wastes containing these. It is recommended to use one or more of the following. The amount added varies depending on the case, but is generally preferably about 0.5 to 20%. The fine powder waste whose chemical composition has been adjusted in this way is molded to increase the number of points of contact between the fine powders, and this molding method can use conventional techniques such as pressurization, rolling, extrusion, etc. . Depending on the molding method, a binder may not necessarily be necessary, but in the present invention, using water as a binder is advantageous for the solidification reaction. in this case,
The amount of water to be added is the optimum amount for each molding method, but in general, in the case of rolling granulation, 20 to 30
%, and in the case of compression molding, about 5 to 15% is effective. The thus formed waste material is heated to 50% at atmospheric pressure.
Solidifies if left in water at temperatures above ℃ or steam at temperatures above 50℃ for 3 days or more. The optimal curing temperature and curing time vary greatly depending on the composition of the waste, etc., but generally 60 to 80°C and 3 to 28 days are economically preferable conditions. In addition, in the present invention, curing in water and curing in steam may be performed together. The mechanism of the reaction that occurs during the curing process is not necessarily clear because it is difficult to identify and quantify the reaction products, but it is possible that calcium silicate hydrate or calcium aluminate hydrate is produced and that fine powders interact with each other due to this. It is thought that the development of strength based on bond progresses. As described above, in the present invention, after the fine powder waste is molded in the presence of a calcium component with addition and mixing of at least one of a solidification accelerator and a reducing agent as required, the pressure is atmospheric pressure and 50°C or higher. By leaving it in water or steam at a temperature of 50℃ or higher for more than 3 days,
It is possible to easily obtain a strong solidified product, improve the hand linkability of the powder, significantly reduce the amount of landfill space, and in some cases, make it possible to reuse it as roadbed material or aggregate. , post-processing can be simplified, and if the heat and steam generated from the waste incineration process are used for heating, it becomes a more energy-saving solidification method, which has an extremely useful effect in preventing pollution, and solves the problems of the past. It also has the advantage of being able to accurately eliminate waste materials, as well as being inexpensive and economical to dispose of. Next, examples of the present invention will be shown. Example 1 Sludge generated at a certain sewage treatment plant was dehydrated by adding slaked lime and ferric chloride, dried, and then incinerated. The composition of incinerated ash was as follows.

【表】 この焼却灰に水を焼却灰重量の15%添加混合
し、1000Kgf/cm2の圧力で直径20mm、長さ20mmの円
板状に圧縮成型し、大気圧下で種々の温度の水蒸
気中に2週間養生して固化物を得た。得られた固
化物の強度と、参考のため各温度の乾燥空気中に
放置した場合の結果を併記した。
[Table] This incinerated ash was mixed with 15% water based on the weight of the incinerated ash, and compressed into a disk shape of 20 mm in diameter and 20 mm in length at a pressure of 1000 Kgf/cm 2 , and steamed at various temperatures under atmospheric pressure. A solidified product was obtained by curing for two weeks. The strength of the obtained solidified product and the results obtained when it was left in dry air at each temperature are also listed for reference.

【表】 上表より、温度50℃以上の水蒸気中で養生する
と固化物強度が著しく増大することがわかる。 実施例 2 某都市ゴミ焼却場EPダストにカルシウム成分
として消石灰を10%、固化促進剤としてけい石粉
末10%を混合し、水分を若干添加して転動造粒機
にて造粒し、含水率25%のグリーンペレツトを得
た。このグリーンペレツトを大気圧下で、50℃水
中及び水蒸気中で養生した結果を第2表に、温度
を変えた水中で養生したときの固化物強度の時間
変化を図面に示す。 第2表より水中でも、水蒸気中でも養生時間が
3日間以上であれば、同じように強度が増大する
ことがわかる。また、図面より養生条件が50℃以
上、3日間以上の領域で強度の大きな固化物が得
られることがわかる。
[Table] From the table above, it can be seen that the strength of the solidified material increases significantly when it is cured in steam at a temperature of 50°C or higher. Example 2 EP dust from a certain municipal waste incinerator was mixed with 10% slaked lime as a calcium component and 10% silica powder as a solidification accelerator, and a small amount of water was added and granulated using a rolling granulator to make it hydrated. Green pellets with a yield of 25% were obtained. Table 2 shows the results of curing these green pellets in water and steam at 50°C under atmospheric pressure, and the figure shows the change in solidified strength over time when curing in water at different temperatures. From Table 2, it can be seen that the strength increases in the same way if the curing time is 3 days or more in water or steam. Furthermore, it can be seen from the drawing that a solidified product with high strength can be obtained under curing conditions of 50°C or higher for 3 days or longer.

【表】 実施例 3 某工場排出処理汚泥を脱水、乾燥、焼却して得
た微粉状焼却灰の化学組成は以下の通りであつ
た。
[Table] Example 3 The chemical composition of finely powdered incineration ash obtained by dehydrating, drying, and incinerating sludge discharged from a certain factory was as follows.

【表】 本試料に還元剤として硫酸第一鉄0.5%と水分
を添加して転動造粒機にて造粒し、含水率20%の
グリーンペレツトを得た。このグリーンペレツト
を大気圧下で70℃の水中の3日間放置して得られ
た固化物の強度と6価クロム溶出量を第3表に示
す。なお強度は直径8〜12mmのものについて測定
した。
[Table] 0.5% ferrous sulfate as a reducing agent and water were added to this sample and granulated using a rolling granulator to obtain green pellets with a water content of 20%. Table 3 shows the strength of the solidified product obtained by leaving the green pellets in water at 70°C under atmospheric pressure for 3 days and the amount of hexavalent chromium eluted. Note that the strength was measured for those with a diameter of 8 to 12 mm.

【表】 第3表より還元剤を添加して水中養生すると固
化物の強度が増大し、6価クロム溶出量も減少す
ることがわかる。
[Table] Table 3 shows that adding a reducing agent and curing in water increases the strength of the solidified product and reduces the amount of hexavalent chromium eluted.

【図面の簡単な説明】[Brief explanation of the drawing]

図面は、本発明の実施例の結果を示すグラフで
ある。
The drawing is a graph showing the results of an example of the present invention.

Claims (1)

【特許請求の範囲】 1 微粉状廃棄物をカルシウム成分の存在下で、
必要に応じて固化促進剤及び/又は還元剤を添加
混合して成型した後、大気圧下で、温度50℃以上
の水又は水蒸気中に3日間以上放置、養生するこ
とを特徴とする微粉状廃棄物の固化処理方法。 2 前記成型工程が水分を併用して行なわれるも
のであつて、該水分の添加量を転動造粒にあつて
は前記廃棄物の乾燥重量の20%〜30%に、圧縮成
型においては5%〜15%にそれぞれ設定して処理
されるものである特許請求の範囲第1項記載の固
化処理方法。 3 前記養生工程の処理時間を3日〜28日とする
特許請求の範囲第1項又は第2項記載の固化処理
方法。 4 前記還元剤の添加量を前記廃棄物の0.5%〜
20%(重量)とする特許請求の範囲第1項、第2
項又は第3項記載の固化処理方法。
[Claims] 1. Processing fine powder waste in the presence of a calcium component,
A fine powder that is characterized by being molded by adding and mixing a solidification accelerator and/or reducing agent as necessary, and then left and cured in water or steam at a temperature of 50°C or higher for 3 days or more under atmospheric pressure. Waste solidification treatment method. 2. If the molding process is performed in combination with water, the amount of water added is 20% to 30% of the dry weight of the waste in the case of rolling granulation, and 5% in the case of compression molding. % to 15%, respectively. 3. The solidification treatment method according to claim 1 or 2, wherein the treatment time of the curing step is 3 days to 28 days. 4 Adjust the amount of the reducing agent added to 0.5% or more of the waste.
20% (by weight) of claims 1 and 2
The solidification treatment method described in Section 3 or Section 3.
JP6507980A 1980-05-16 1980-05-16 Caking of pulverized waste Granted JPS56161880A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6507980A JPS56161880A (en) 1980-05-16 1980-05-16 Caking of pulverized waste

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6507980A JPS56161880A (en) 1980-05-16 1980-05-16 Caking of pulverized waste

Publications (2)

Publication Number Publication Date
JPS56161880A JPS56161880A (en) 1981-12-12
JPS6134873B2 true JPS6134873B2 (en) 1986-08-09

Family

ID=13276580

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6507980A Granted JPS56161880A (en) 1980-05-16 1980-05-16 Caking of pulverized waste

Country Status (1)

Country Link
JP (1) JPS56161880A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109646861B (en) * 2019-02-02 2020-06-30 常熟理工学院 A method for simultaneously realizing detoxification of incineration fly ash and reduction and solidification of chromium slag

Also Published As

Publication number Publication date
JPS56161880A (en) 1981-12-12

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