JP2014083491A - Processing method for combustion ash - Google Patents

Processing method for combustion ash Download PDF

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JP2014083491A
JP2014083491A JP2012233704A JP2012233704A JP2014083491A JP 2014083491 A JP2014083491 A JP 2014083491A JP 2012233704 A JP2012233704 A JP 2012233704A JP 2012233704 A JP2012233704 A JP 2012233704A JP 2014083491 A JP2014083491 A JP 2014083491A
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combustion ash
ash
combustion
paper sludge
elution
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Masatoshi Oishi
正淳 大石
Hiroaki Tada
裕亮 多田
Yuki Kawamata
友紀 川真田
Yuji Ono
裕司 小野
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Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
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Nippon Paper Industries Co Ltd
Jujo Paper Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a method for treating the paper sludge combustion ash containing harmful substances effectively and conveniently.SOLUTION: Combustion ash is treated to attain a product by adding 0.01 to 2 pts.wt. of sulfite salt to 100 pts.wt. of combustion ash containing paper sludge combustion ash having a particle size adjusted within 10 to 300 μm. This product is suppressed in the elution of noxious components so that the product can be effective in applications of an absorber, a soil improvement material, a roadbed material, a forest work and a road improvement material, and the like.

Description

本発明は、ペーパースラッジ燃焼灰を含む燃焼灰を処理する方法に関する。特に本発明の処理方法を適用することにより、フッ素や六価クロム等の無機有害成分が燃焼灰から溶出することを抑制でき、かつ同時に燃焼灰の飛散防止も図ることができる。また、本発明によれば、被処理物である燃焼灰の吸水性が維持された処理物が得られるため、処理物を高い吸水性を持つ土壌改良材、吸水材などとして利用できる。   The present invention relates to a method for treating combustion ash including paper sludge combustion ash. In particular, by applying the treatment method of the present invention, inorganic harmful components such as fluorine and hexavalent chromium can be prevented from eluting from the combustion ash, and at the same time, the combustion ash can be prevented from scattering. In addition, according to the present invention, a treated product in which the water absorption of the combustion ash that is the object to be treated is maintained can be obtained, so that the treated product can be used as a soil improving material, a water absorbing material, or the like having high water absorption.

近年、環境保全の観点から、産業廃棄物の削減が強く求められている。産業廃棄物の削減は、発電や廃棄物焼却等を行っている全ての企業及び自治体に対する要請であり、紙・パルプ業界もその例外ではない。   In recent years, reduction of industrial waste has been strongly demanded from the viewpoint of environmental conservation. The reduction of industrial waste is a request to all companies and local governments that are engaged in power generation and waste incineration, and the paper and pulp industry is no exception.

このような状況の中、燃焼灰の取り扱いが大きな社会問題となっている。現在、燃焼灰は、その一部が、セメント原料や製鉄用酸化防止剤、混和剤などの再生材料として有効利用されているが、残りは産業廃棄物として埋め立てられることが多い。再利用があまり進んでいない原因として、燃焼灰は土壌汚染対策法施行規則(平成十四年環境省令第二十九号)第五条第三項第四号の規定に基づき定められた土壌環境基準(環境省告示第十八号、改正環境省告示第四十八号)に挙げられている有害成分の溶出量が基準値を超過することが多いことがある。上記有害成分のうち、有機物有害成分は焼却時に分解されるため、燃焼灰ではほとんどの場合問題とはならないが、フッ素、ほう素、六価クロム、鉛をはじめとする無機物有害成分の溶出量は基準を超過することが多い。有害成分溶出量が土壌環境基準値を超過している場合、その燃焼灰は土壌に施用することができず、再利用を図る上で大きな障壁となっている。   Under such circumstances, handling of combustion ash is a big social problem. Currently, a part of the combustion ash is effectively used as a recycled material such as a cement raw material, an iron-making antioxidant and an admixture, but the rest is often landfilled as industrial waste. Combustion ash is one of the reasons for not reusing the soil environment in accordance with the provisions of Article 5, Paragraph 4, Item 4 of the Ordinance for Enforcement of the Soil Contamination Countermeasures Law (Ministry of Environment Ordinance No. 29, 2004). In many cases, the elution amount of harmful components listed in the standards (Ministry of the Environment Notification No. 18 and Amended Ministry of the Environment Notification No. 48) exceeds the standard value. Of the above harmful components, organic harmful components are decomposed during incineration, so combustion ash is not a problem in most cases, but the amount of elution of inorganic harmful components such as fluorine, boron, hexavalent chromium and lead is Often the standard is exceeded. If the leaching amount of harmful components exceeds the soil environment standard value, the combustion ash cannot be applied to the soil, which is a big barrier to reuse.

また、ほとんどの場合、燃焼灰は細かい固体状の粉末であり、取り扱う上で粉塵としての注意も要する。排出や輸送を行う際に、粉塵飛散防止を図るため燃焼灰に水分を添加することが一般に行われているが、水分を添加した燃焼灰を大気中に放置しておくと、添加された水分が燃焼灰中のカルシウム分と反応して水酸化カルシウムが形成され、この水酸化カルシウムが大気中の二酸化炭素と反応することにより炭酸カルシウムとなるため、燃焼灰の溶出pHが低下し、結果として六価クロムの溶出量が増大する。また、多量の水分添加により燃焼灰の吸水性が低下してしまうため、燃焼灰の優れた吸水性を生かして吸水性製品として再利用する際に再利用製品の性能が低下するという問題もある。   Further, in most cases, the combustion ash is a fine solid powder and requires attention as dust when handled. When discharging or transporting, it is common to add moisture to the combustion ash to prevent dust scattering, but if the combustion ash with added moisture is left in the air, the added moisture Reacts with the calcium content in the combustion ash to form calcium hydroxide, and this calcium hydroxide reacts with carbon dioxide in the atmosphere to form calcium carbonate. The elution amount of hexavalent chromium increases. In addition, since the water absorption of combustion ash is reduced due to the addition of a large amount of water, there is also a problem that the performance of the reused product is reduced when it is reused as a water absorbent product utilizing the excellent water absorption of combustion ash. .

土壌汚染対策法に規定される土壌環境基準を満足すべく、被汚染物に何らかの不溶化剤を添加して有害成分溶出量の低下を図る技術は、これまでに数多く検討され、特許出願もなされている。特許文献1には、6価クロム汚染土壌をポリフェノール、及びリン酸またはリン酸塩と接触させることによる汚染土壌の処理方法が開示されている。特許文献2には、有機塩素化合物により汚染され、重金属類を含む汚染物に、酸化剤として過硫酸塩を添加した後に還元剤を添加することを特徴とする化学物質による汚染の浄化方法が開示されている。また、特許文献3には、フッ素及びホウ素を含有する燃焼灰に、酸化カルシウム、高炉セメント、硫酸アルミニウムを水の存在下で加えて混合処理することにより、フッ素及びホウ素の溶出量を抑制する方法が開示されている。   In order to satisfy the soil environmental standards stipulated in the Soil Contamination Countermeasures Law, a number of technologies have been studied and patent applications have been made to reduce the leaching amount of harmful components by adding some insolubilizing agent to contaminated materials. Yes. Patent Document 1 discloses a method for treating contaminated soil by contacting hexavalent chromium-contaminated soil with polyphenol and phosphoric acid or phosphate. Patent Document 2 discloses a method for purifying contamination caused by a chemical substance, characterized by adding a reducing agent after adding a persulfate as an oxidizing agent to a contaminant containing an organic chlorine compound and containing heavy metals. Has been. Patent Document 3 discloses a method for suppressing the elution amount of fluorine and boron by adding calcium oxide, blast furnace cement, and aluminum sulfate in the presence of water to combustion ash containing fluorine and boron and mixing the mixture. Is disclosed.

特開平10−85716号公報Japanese Patent Application Laid-Open No. 10-85716 特開2004−337777号公報(特許第4095490号公報)JP 2004-337777 A (Patent No. 4095490) 特開2006−181535号公報JP 2006-181535 A

本発明の主たる課題は、有害物質を含むペーパースラッジ燃焼灰を有効かつ簡便に処理する方法を提供することである。特に、ペーパースラッジ燃焼灰に含まれるフッ素や六価クロム等の無機有害成分の溶出量を低減し、かつ同時に被処理物の吸水性を損なわないように処理を行うことによって、処理物を高い吸水性を持つ吸水性材料などとしても利用できるような、付加価値のある処理物を得ることも目的とする。   The main subject of this invention is providing the method of processing the paper sludge combustion ash containing a harmful substance effectively and simply. In particular, by reducing the elution amount of inorganic harmful components such as fluorine and hexavalent chromium contained in paper sludge combustion ash, and at the same time, processing so as not to impair the water absorption of the object to be treated, the treated material has high water absorption. Another object of the present invention is to obtain a treated product with added value that can be used as a water-absorbing material having a property.

本発明は、ペーパースラッジ燃焼灰を含む燃焼灰の粒径を、10〜300μmの範囲に調整した後、亜硫酸塩を添加することを含む、燃焼灰の処理方法である。   The present invention is a method for treating combustion ash, which includes adding sulfite after adjusting the particle size of combustion ash containing paper sludge combustion ash to a range of 10 to 300 μm.

本発明により、有害物質を含む廃棄物であるペーパースラッジ燃焼灰を効率的かつ簡便に処理する方法が提供される。特に本発明によれば、ペーパースラッジ燃焼灰に含まれるフッ素や六価クロム等の無機有害成分の溶出を抑制できる。また本発明によれば、吸水性材料などとしても利用できるような付加価値のある処理物を、燃焼灰を原料として製造することができる。本発明においては、特別な装置または機器を必要とせず、薬品を添加するのみの比較的シンプルな工程で、ペーパースラッジ燃焼灰の処理を完結させることができる。   The present invention provides a method for efficiently and simply treating paper sludge combustion ash, which is a waste containing hazardous substances. In particular, according to the present invention, elution of inorganic harmful components such as fluorine and hexavalent chromium contained in the paper sludge combustion ash can be suppressed. Moreover, according to this invention, the processed material with added value which can be utilized also as a water absorbing material etc. can be manufactured by using combustion ash as a raw material. In the present invention, it is possible to complete the treatment of the paper sludge combustion ash by a relatively simple process in which only a chemical is added without requiring a special device or equipment.

本発明においてペーパースラッジとは製紙スラッジとも呼ばれ、パルプ製造工程、紙製造工程、古紙処理工程などから発生する廃棄物を意味する。ペーパースラッジには、顔料や填料として製紙に使用されるシリカ、炭酸カルシウム、硅砂、タルク、カオリンなどの無機物質に加え、パルプ、インク、製紙用薬品などの有機物質が含有される。   In the present invention, the paper sludge is also called paper sludge and means waste generated from a pulp manufacturing process, a paper manufacturing process, a used paper processing process, and the like. Paper sludge contains organic substances such as pulp, ink, and papermaking chemicals in addition to inorganic substances such as silica, calcium carbonate, cinnabar, talc and kaolin used in papermaking as pigments and fillers.

本発明においてペーパースラッジ燃焼灰とは、ペーパースラッジを燃焼装置で燃焼処理した際に発生する燃焼灰のことである。   In the present invention, paper sludge combustion ash refers to combustion ash generated when paper sludge is burned by a combustion device.

本発明において燃焼装置の形式などは特に限定されず、公知の装置を使用することができる。例えば、流動層ボイラーやストーカ燃焼炉などの公知の焼却装置などを挙げることができる。   In the present invention, the type of the combustion apparatus is not particularly limited, and a known apparatus can be used. For example, a known incinerator such as a fluidized bed boiler or a stoker combustion furnace can be used.

また、助燃用とするため、重油や石炭などの燃料をペーパースラッジと共に混焼しても構わない。さらに、RDF(ごみ固形燃料)、RPF(産業系廃プラスチック・古紙類固形燃料)、その他の一般可燃物もペーパースラッジと共に、ボイラーで混焼することは構わない。   Moreover, in order to use for auxiliary combustion, fuels such as heavy oil and coal may be mixed with paper sludge. Furthermore, RDF (garbage solid fuel), RPF (industrial waste plastic / waste paper solid fuel), and other general combustible materials may be co-fired in a boiler together with paper sludge.

上記の燃焼処理を施す際の温度は当業者が任意に決めることができ、500〜1500℃の範囲が好ましく、600〜1200℃の範囲がより好ましく、700〜1000℃の範囲が最も好ましい。また、上記燃焼処理の時間も適宜選択することができ、燃焼装置における原料の平均滞留時間は、1時間以内が好ましく、3〜30分間以内がより好ましく、10分間以内がさらに好ましい。   The temperature at which the above combustion treatment is performed can be arbitrarily determined by those skilled in the art, preferably in the range of 500 to 1500 ° C, more preferably in the range of 600 to 1200 ° C, and most preferably in the range of 700 to 1000 ° C. Moreover, the time of the said combustion process can also be selected suitably, The average residence time of the raw material in a combustion apparatus has preferable within 1 hour, More preferably within 3-30 minutes, More preferably within 10 minutes.

本発明においては、ペーパースラッジ燃焼灰に加えて、石炭灰、バイオマス燃焼灰をさらに混合して使用してもよい。石炭灰、バイオマス燃焼灰の混合比率は、ペーパースラッジ燃焼灰100質量部に対して0〜100質量部が好ましく、0〜50質量部がより好ましい。   In the present invention, in addition to paper sludge combustion ash, coal ash and biomass combustion ash may be further mixed and used. 0-100 mass parts is preferable with respect to 100 mass parts of paper sludge combustion ash, and, as for the mixing ratio of coal ash and biomass combustion ash, 0-50 mass parts is more preferable.

このようにして得られた燃焼灰に対し、本発明においては、後述の薬品添加前に、燃焼灰に何らかの処理を行うこともできる。例えば、本発明の目的を損なわない範囲において、粉砕、破砕、解砕、分級、再燃焼、再乾燥、磁力選別などの前処理を、当業者に周知のあらゆる適切な装置を用いて、焼却灰に対して行うこともできる。別法として、燃焼処理された燃焼灰に何らかの前処理を行わずに、そのまま本発明に利用することもでき、消費エネルギー及びコストの観点から、前処理を行わないことが好ましい。   In the present invention, the combustion ash obtained in this way can be subjected to some kind of treatment before the chemical addition described below. For example, insofar as the object of the present invention is not impaired, pretreatment such as crushing, crushing, crushing, classification, reburning, redrying, magnetic sorting, etc. is performed using any suitable apparatus well known to those skilled in the art. Can also be done. Alternatively, the combustion ash that has been subjected to the combustion treatment can be directly used in the present invention without performing any pretreatment, and it is preferable not to perform the pretreatment from the viewpoint of energy consumption and cost.

本発明においては、燃焼灰の粒径を10〜300μm、好ましくは150〜250μm、さらに好ましくは150〜250μmの範囲とする。燃焼灰の粒径が大きくなると比表面積は小さくなり、結果、フッ素、ホウ素の溶出量が減少する。しかし、燃焼灰の粒径が300μmを超えると強度が低下するので、路盤材、森林作業道改良材等の用途には好ましくない。   In the present invention, the particle size of the combustion ash is 10 to 300 μm, preferably 150 to 250 μm, and more preferably 150 to 250 μm. As the particle size of the combustion ash increases, the specific surface area decreases, and as a result, the amount of fluorine and boron eluted decreases. However, if the particle size of the combustion ash exceeds 300 μm, the strength decreases, which is not preferable for applications such as roadbed materials and forest road improvement materials.

本発明において、燃焼灰の粒径を調整する装置としては、振動篩、超音波篩、ジェットスクリーン、エアセパレーター、トロンメルスクリーン、サイクロン型の風力式分級機等が挙げられる。具体的には、風力式分級機(ミクロンセパレーター、ホソカワミクロン(株)製)、半自由渦遠心式分級機(エディクラシファイア、日清エンジニアリング(株)製)が挙げられる。   In the present invention, the apparatus for adjusting the particle size of the combustion ash includes a vibrating sieve, an ultrasonic sieve, a jet screen, an air separator, a trommel screen, a cyclone type wind classifier, and the like. Specific examples include a wind classifier (micron separator, manufactured by Hosokawa Micron Corporation), and a semi-free vortex centrifugal classifier (eddy classifier, manufactured by Nisshin Engineering Co., Ltd.).

本発明においては、亜硫酸塩を添加することが好ましい。亜硫酸塩を添加することで六価クロムの溶出量を抑制できる。亜硫酸塩としては、亜硫酸ナトリウム、亜硫酸カリウムが挙げられる。亜硫酸塩は燃焼灰100質量部に対して0.01〜5質量部添加することが必要で、0.1〜1質量部添加することがさらに好ましい。添加量が0.01質量部未満であると六価クロムの溶出量の抑制が不十分であり、5質量部を超えて添加しても効果は向上しない。亜硫酸塩を添加することにより、六価クロムが無害な三価クロムに還元されて六価クロムの溶出量が減少すると考えられる。   In the present invention, sulfite is preferably added. The elution amount of hexavalent chromium can be suppressed by adding sulfite. Examples of the sulfite include sodium sulfite and potassium sulfite. It is necessary to add 0.01 to 5 parts by mass of sulfite to 100 parts by mass of combustion ash, and it is more preferable to add 0.1 to 1 part by mass. When the addition amount is less than 0.01 parts by mass, the suppression of the elution amount of hexavalent chromium is insufficient, and even if the addition amount exceeds 5 parts by mass, the effect is not improved. By adding sulfite, it is considered that hexavalent chromium is reduced to harmless trivalent chromium and the elution amount of hexavalent chromium is reduced.

本発明においては上記の原料を混練して処理物を製造する。混練時間は、混合装置(撹拌子の回転数や大きさ等)にも影響されるため、適宜調節することが好ましいが、1〜30分間が望ましく、5〜10分間がより望ましい。混練するための混合装置は特に制限されず、混練ロールや混練羽根を備えた装置によって上記原料を混練することができるが、効率よく混練するためには転動混練機が最も好適である。好適な混練機の例として、ELBAミキサー(クリハラ製)、インテンシブミキサー(アイリッヒ製)、ペレガイア(北川鉄工所製)等が挙げられる。   In the present invention, the above raw materials are kneaded to produce a processed product. The kneading time is also affected by the mixing device (such as the rotation speed and size of the stirrer), and thus is suitably adjusted, but is preferably 1 to 30 minutes, and more preferably 5 to 10 minutes. The mixing apparatus for kneading is not particularly limited, and the raw material can be kneaded by an apparatus equipped with a kneading roll and a kneading blade, but a rolling kneader is most suitable for efficient kneading. Examples of suitable kneaders include ELBA mixers (manufactured by Kurihara), intensive mixers (manufactured by Eirich), and Pelegaia (manufactured by Kitagawa Iron Works).

なお、本発明においては、ペーパースラッジ燃焼灰、亜硫酸塩などの原料を混練機に別々に供給してもよく、予め混合した状態で供給してもよい。   In the present invention, raw materials such as paper sludge combustion ash and sulfite may be supplied separately to the kneader, or may be supplied in a premixed state.

本発明において、必ずしも燃焼灰に水を添加しなくてもよい。飛散性の防止のために水を添加する場合には、燃焼灰100重量部に対して30重量部以下とすることが望ましい。30重量部を超えて添加すると、燃焼灰自体が多量の水分を含むことになり焼却灰の吸水性が失われてしまい、得られた処理物を吸水材などに利用することが困難となることがある。また、水分を多く添加した燃焼灰は六価クロムの溶出量が多くなる傾向がある。   In the present invention, it is not always necessary to add water to the combustion ash. When water is added to prevent scattering, the amount is preferably 30 parts by weight or less with respect to 100 parts by weight of combustion ash. If the amount exceeds 30 parts by weight, the combustion ash itself contains a large amount of water, and the water absorption of the incinerated ash is lost, making it difficult to use the obtained processed product as a water absorbent. There is. Further, combustion ash to which a large amount of moisture is added tends to increase the elution amount of hexavalent chromium.

本発明によって得られる処理物は、吸水性が良好であり、それ自体有用なものである。本発明の処理物は、その吸水性や保水性を活かして、例えば、吸収材、土壌改良材、路盤材、森林作業道改良材などの用途に特に好適に使用することができる。本発明によれば、廃棄物である燃焼灰を原料として有用材料を製造することができるため、廃棄物削減、地球環境保全の観点からも好適である。   The treated product obtained by the present invention has good water absorption and is useful per se. The treated product of the present invention can be particularly suitably used for applications such as an absorbent material, a soil improvement material, a roadbed material, and a forest work road improvement material, taking advantage of its water absorption and water retention. According to the present invention, a useful material can be produced using combustion ash, which is waste, as a raw material, which is preferable from the viewpoint of waste reduction and global environmental conservation.

以下、本発明の実施例を比較例と対比しつつ具体的に説明するが、本発明はこれらに限定されるものではない。   Examples of the present invention will be specifically described below in comparison with comparative examples, but the present invention is not limited to these examples.

なお、説明中、「%」および「部」は特に断らない限り、「質量%」および「質量部」を示す。また、材料添加率については、特に指定が無い場合は、有効成分の添加率を示す。
(A)フッ素(F)、ホウ素(B)、六価クロム(Cr(VI)、全クロム(全Cr)、鉛(Pb)の溶出方法:平成15年環境省告示第18号に準じて行なった。すなわち、試料を、粒状品は破砕した後、非金属製である目開き2mmの篩を通過させたもの50gを1000mlの蓋つきのポリエチレン容器に取り、純水(pH5.8〜6.3)を500ml加えて試料液を調製した。この調製した試料液を、常温、大気圧下で、溶出振とう機を用いて6時間連続振とうした(振とう幅4〜5cm、振動数200回/分)。ついで、振とう後の試料液を、30分間静置した後、毎分約3000回転で20分間遠心分離した。上澄み液を孔径0.45μmのメンブレンフィルターで濾過し、濾液をとり、定量に必要な量を正確に計り取り、これを検液とした。なお、溶出量基準はフッ素0.8mg/L以下、ホウ素1mg/L以下、六価クロム0.05mg/L以下、鉛0.01mg/L以下である。
(B)フッ素溶出量の測定方法:上記検液をイオンクロマトグラフ法により分析し、溶出したフッ素の量を定量した(JIS K 0102の34.2)。
(C)ホウ素、六価クロム、全クロム、鉛溶出量の測定方法:上記検液をジフェニルカルバジド吸光光度法にて分析し、溶出したホウ素、六価クロム、全クロム、鉛の量を定量した(JIS K 0102の65.2.1)。
(D)溶出液のpH:「土懸濁液のpH試験方法」(地盤工学会基準、JGS 0211-2000)に従って、試料に対して5倍量の水を加えて撹拌した試料液のpHを測定した。
In the description, “%” and “part” indicate “% by mass” and “part by mass” unless otherwise specified. Moreover, about the material addition rate, when there is no designation | designated, the addition rate of an active ingredient is shown.
(A) Fluorine (F), boron (B), hexavalent chromium (Cr (VI), total chromium (total Cr), lead (Pb) elution method: performed in accordance with 2003 Ministry of the Environment Notification No. 18 That is, after the sample was crushed into granular products, 50 g of a non-metallic sieve having a mesh opening of 2 mm was passed into a 1000 ml polyethylene container with a lid, and purified water (pH 5.8 to 6.3) was obtained. The sample solution was shaken continuously for 6 hours at room temperature and atmospheric pressure using an elution shaker (shaking width: 4 to 5 cm, frequency: 200 times). The sample solution after shaking was allowed to stand for 30 minutes, and then centrifuged at about 3000 rpm for 20 minutes, and the supernatant was filtered through a membrane filter having a pore size of 0.45 μm. Measure accurately the amount required for quantification, It was used as a test liquid. Incidentally, elution reference the following fluorine 0.8 mg / L, or less boron 1 mg / L, hexavalent chromium 0.05 mg / L or less, or less lead 0.01 mg / L.
(B) Method for measuring fluorine elution amount: The above test solution was analyzed by ion chromatography, and the amount of eluted fluorine was quantified (34.2 of JIS K 0102).
(C) Measuring method for elution amount of boron, hexavalent chromium, total chromium and lead: Analyze the above test solution by diphenylcarbazide absorptiometry and quantify the amount of eluted boron, hexavalent chromium, total chromium and lead (JIS K 0102 65.2.1).
(D) pH of eluate: according to “pH test method for soil suspension” (Geotechnical Society standard, JGS 0211-2000) It was measured.

[実施例1]
製紙工場における脱墨フロスおよび流失繊維を主体とする廃棄物(以下「ペーパースラッジ」と呼ぶ)を、燃焼温度850℃、平均滞留時間が10秒未満の条件でペーパースラッジ用流動床炉にて燃焼させた。この燃焼は、廃棄物の減容化ならびに蒸気および熱エネルギーの回収を目的とするものである。
得られた燃焼残渣(燃焼灰)はサイクロン処理で大粒径部分を捕集した後、小粒径部分をバグフィルタに捕集する。最終的に貯蔵サイロ内へ移送された燃焼灰を取り出し、以下の処理に供した。
サイクロン処理した平均粒径が206.4μmの燃焼灰100部に対し、亜硫酸ナトリウムを0.25部添加し、ミキサーを用いて3分間撹拌、混合した。処理後の灰について、平成15年環境省告示第18号に準拠し、溶出試験を行った。溶出液のpHは12.0、フッ素の溶出量は0.55mg/L、六価クロムの溶出量は0.018mg/Lであり、その他の元素の溶出量も土壌汚染対策法の環境基準値以下であった。
[Example 1]
Burning waste (mainly referred to as “paper sludge”) consisting mainly of deinked floss and run-off fibers in a paper mill in a fluidized bed furnace for paper sludge at a combustion temperature of 850 ° C. and an average residence time of less than 10 seconds I let you. This combustion is intended to reduce the volume of waste and recover steam and thermal energy.
The obtained combustion residue (combustion ash) collects a large particle size portion by a cyclone treatment, and then collects a small particle size portion in a bag filter. The combustion ash finally transferred into the storage silo was taken out and subjected to the following treatment.
0.25 part of sodium sulfite was added to 100 parts of combustion ash having an average particle diameter of 206.4 μm treated with cyclone, and the mixture was stirred and mixed for 3 minutes using a mixer. The ash after the treatment was subjected to a dissolution test in accordance with 2003 Ministry of the Environment Notification No.18. The pH of the eluate is 12.0, the elution amount of fluorine is 0.55 mg / L, the elution amount of hexavalent chromium is 0.018 mg / L, and the elution amounts of other elements are the environmental standard values of the Soil Contamination Countermeasures Law. It was the following.

[実施例2]
燃焼灰100部に対して亜硫酸ナトリウムを0.5部添加した以外は、実施例1と同様にして処理を行った。処理後の灰について、平成15年環境省告示第18号に準拠し、溶出試験を行った。溶出液のpHは12.0、フッ素の溶出量は0.54mg/L、六価クロムの溶出量は0.03mg/Lであり、その他の元素の溶出量も土壌汚染対策法の環境基準値以下であった。
[Example 2]
The treatment was performed in the same manner as in Example 1 except that 0.5 part of sodium sulfite was added to 100 parts of combustion ash. The ash after the treatment was subjected to a dissolution test in accordance with 2003 Ministry of the Environment Notification No.18. The pH of the eluate is 12.0, the elution amount of fluorine is 0.54 mg / L, the elution amount of hexavalent chromium is 0.03 mg / L, and the elution amount of other elements is also the environmental standard value of the soil pollution countermeasures law. It was the following.

[比較例1]
燃焼灰100部に対して亜硫酸ナトリウムを0.1部添加した以外は、実施例1と同様にして処理を行った。処理後の灰について、平成15年環境省告示第18号に準拠し、溶出試験を行った。溶出液のpHは11.9、フッ素の溶出量は0.50mg/L、六価クロムの溶出量は0.053mg/Lであった。その他の元素の溶出量は土壌汚染対策法の環境基準値以下であった。
[Comparative Example 1]
The treatment was performed in the same manner as in Example 1 except that 0.1 part of sodium sulfite was added to 100 parts of combustion ash. The ash after the treatment was subjected to a dissolution test in accordance with 2003 Ministry of the Environment Notification No.18. The pH of the eluate was 11.9, the elution amount of fluorine was 0.50 mg / L, and the elution amount of hexavalent chromium was 0.053 mg / L. The amount of elution of other elements was below the environmental standard value of the Soil Contamination Countermeasures Law.

[比較例2]
亜硫酸ナトリウムを添加しない以外は、実施例1と同様にして処理を行った。処理後の灰について、平成15年環境省告示第18号に準拠し、溶出試験を行った。溶出液のpHは12.0、フッ素の溶出量は0.27mg/L、六価クロムの溶出量は0.079mg/Lであった。その他の元素の溶出量は土壌汚染対策法の環境基準値以下であった。
[Comparative Example 2]
The treatment was performed in the same manner as in Example 1 except that sodium sulfite was not added. The ash after the treatment was subjected to a dissolution test in accordance with 2003 Ministry of the Environment Notification No.18. The pH of the eluate was 12.0, the elution amount of fluorine was 0.27 mg / L, and the elution amount of hexavalent chromium was 0.079 mg / L. The amount of elution of other elements was below the environmental standard value of the Soil Contamination Countermeasures Law.

[比較例3]
バグフィルタに捕集された平均粒径が6.2μmの燃焼灰の灰について、平成15年環境省告示第18号に準拠し、溶出試験を行った。溶出液のpHは11.1、フッ素の溶出量は2.24mg/L、ホウ素の溶出量は1.12mg/L、六価クロムの溶出量は0.060mg/Lであった。その他の元素の溶出量は土壌汚染対策法の環境基準値以下であった。
[Comparative Example 3]
The ash of combustion ash with an average particle size of 6.2 μm collected by the bag filter was subjected to an elution test in accordance with Notification No. 18 of the Ministry of the Environment in 2003. The pH of the eluate was 11.1, the elution amount of fluorine was 2.24 mg / L, the elution amount of boron was 1.12 mg / L, and the elution amount of hexavalent chromium was 0.060 mg / L. The amount of elution of other elements was below the environmental standard value of the Soil Contamination Countermeasures Law.

Figure 2014083491
Figure 2014083491

実施例1〜2と比較例1〜3を比較することから明らかなように、本発明によって焼却灰から得られた処理物は、有害物質が溶出しにくかった。すなわち、フッ素および六価クロムを含む焼却灰に、サイクロン処理後に亜硫酸塩を適量、添加・混合処理することにより、平成15年環境省告示第18号に基づく溶出試験による該焼却灰からのフッ素の溶出量を0.8mg/L未満、かつ六価クロムの溶出量を0.05mg/L未満にすることができる。これにより、焼却灰からの全ての環境影響元素の溶出量を土壌汚染対策法の環境基準値以下にでき、フッ素および六価クロムを含む焼却灰を安全に土壌分野へ利用することが可能になった。   As is clear from a comparison of Examples 1 and 2 and Comparative Examples 1 to 3, the treated product obtained from the incinerated ash according to the present invention was difficult to elute harmful substances. In other words, an appropriate amount of sulfite is added to and mixed with incinerated ash containing fluorine and hexavalent chromium after cyclone treatment, so that fluorine from the incinerated ash by an elution test based on Notification No. 18 of the Ministry of the Environment in 2003 can be obtained. The elution amount can be less than 0.8 mg / L, and the elution amount of hexavalent chromium can be less than 0.05 mg / L. As a result, the amount of elution of all environmental impact elements from the incineration ash can be reduced below the environmental standard value of the Soil Contamination Countermeasures Law, and incineration ash containing fluorine and hexavalent chromium can be safely used in the soil field. It was.

Claims (4)

ペーパースラッジ燃焼灰を含む燃焼灰の粒径を10〜300μmの範囲に調整した後、亜硫酸塩を添加することを含む、燃焼灰の処理方法。   A method for treating combustion ash, comprising adjusting the particle size of combustion ash containing paper sludge combustion ash to a range of 10 to 300 μm and then adding sulfite. ペーパースラッジ燃焼灰を含む燃焼灰100質量部に対して、亜硫酸塩を0.01〜5質量部の範囲で添加する請求項1に記載の燃焼灰の処理方法。   The processing method of the combustion ash of Claim 1 which adds a sulfite in the range of 0.01-5 mass parts with respect to 100 mass parts of combustion ash containing paper sludge combustion ash. 前記燃焼灰が、ペーパースラッジ燃焼灰100質量部に対して石炭灰を0〜50重量部含む、請求項1〜2のいずれかに記載の燃焼灰の処理方法。   The processing method of the combustion ash in any one of Claims 1-2 in which the said combustion ash contains 0-50 weight part of coal ash with respect to 100 mass parts of paper sludge combustion ash. サイクロン処理することによって、ペーパースラッジ燃焼灰を含む燃焼灰の粒径を10〜300μmの範囲に調整することを含む、請求項1〜3のいずれかに記載の燃焼灰の処理方法。   The processing method of the combustion ash in any one of Claims 1-3 including adjusting the particle size of the combustion ash containing paper sludge combustion ash to the range of 10-300 micrometers by performing a cyclone process.
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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08267046A (en) * 1995-03-29 1996-10-15 Komatsu Ltd Treatment of waste
JP2002079207A (en) * 2000-09-05 2002-03-19 Penta Ocean Constr Co Ltd Method for classifying incineration bottom ash and land- filling sea level site with this bottom ash
US20020155058A1 (en) * 2001-01-26 2002-10-24 Tosoh Corporation Iron sulfides, processes for producing the same, iron sulfide mixture, heavy metal treating agent, and method of treating with the agent
JP2003253138A (en) * 2002-03-06 2003-09-10 Maruwa Kasei Kk Method for manufacturing plastic molded article mixed with incineration ash of papermaking sludge
JP2004209372A (en) * 2002-12-27 2004-07-29 Ebara Corp Heavy metal elution inhibitor and heavy metal elution inhibiting method
JP2007245016A (en) * 2006-03-16 2007-09-27 Kawasaki Heavy Ind Ltd Treating method of waste incineration ash, substitute material for sand obtained by using the method, and substitute material for ballast
JP2008272574A (en) * 2007-01-12 2008-11-13 Chugoku Electric Power Co Inc:The Method of suppressing elution of hexavalent chromium and thermal power generation system
JP2010222430A (en) * 2009-03-23 2010-10-07 Daio Paper Corp Soil-improving material and method for producing the same

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08267046A (en) * 1995-03-29 1996-10-15 Komatsu Ltd Treatment of waste
JP2002079207A (en) * 2000-09-05 2002-03-19 Penta Ocean Constr Co Ltd Method for classifying incineration bottom ash and land- filling sea level site with this bottom ash
US20020155058A1 (en) * 2001-01-26 2002-10-24 Tosoh Corporation Iron sulfides, processes for producing the same, iron sulfide mixture, heavy metal treating agent, and method of treating with the agent
JP2003253138A (en) * 2002-03-06 2003-09-10 Maruwa Kasei Kk Method for manufacturing plastic molded article mixed with incineration ash of papermaking sludge
JP2004209372A (en) * 2002-12-27 2004-07-29 Ebara Corp Heavy metal elution inhibitor and heavy metal elution inhibiting method
JP2007245016A (en) * 2006-03-16 2007-09-27 Kawasaki Heavy Ind Ltd Treating method of waste incineration ash, substitute material for sand obtained by using the method, and substitute material for ballast
JP2008272574A (en) * 2007-01-12 2008-11-13 Chugoku Electric Power Co Inc:The Method of suppressing elution of hexavalent chromium and thermal power generation system
JP2010222430A (en) * 2009-03-23 2010-10-07 Daio Paper Corp Soil-improving material and method for producing the same

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