JP2020179353A - Waste incineration system - Google Patents

Waste incineration system Download PDF

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JP2020179353A
JP2020179353A JP2019084470A JP2019084470A JP2020179353A JP 2020179353 A JP2020179353 A JP 2020179353A JP 2019084470 A JP2019084470 A JP 2019084470A JP 2019084470 A JP2019084470 A JP 2019084470A JP 2020179353 A JP2020179353 A JP 2020179353A
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hydrogen chloride
treatment agent
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JP7264372B2 (en
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豊 松原
Yutaka Matsubara
豊 松原
剛太郎 月川
Gotaro Tsukikawa
剛太郎 月川
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Akagi Koyu Co Ltd
Japan Metals and Chemical Co Ltd
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Japan Metals and Chemical Co Ltd
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Abstract

To provide a waste incineration system capable of controlling more easily discharge of dioxins in exhaust gas.SOLUTION: A waste incineration system includes dust collection means, treatment agent supply means provided on the upstream of the dust collection means, for supplying a treatment agent, hydrogen chloride concentration measurement means for measuring continuously a hydrogen chloride concentration in exhaust gas, and treatment agent supply control means for controlling supply of the treatment agent. In the waste incineration system, the treatment agent contains an adsorbent having a function for adsorbing dioxins in exhaust gas, and the treatment agent supply control means controls a supply period of the treatment agent based on a mean value of the hydrogen chloride concentration.SELECTED DRAWING: Figure 1

Description

本発明は、廃棄物焼却システムに関する。 The present invention relates to a waste incineration system.

ダイオキシン類対策特別措置法に基づき、平成14年12月1日より全ての廃棄物焼却システムに施設規模に応じて排ガス中のダイオキシン類濃度の排出基準が課せられた。ダイオキシン類等の有害物質の発生を抑制するため、各廃棄物焼却システムでは高温燃焼状態を保ち、焼却後は速やかに減温処理することで、ダイオキシン類の合成を抑える等の措置が取られている。万一、減温処理過程において、ダイオキシン類が再合成された場合には、燃焼により発生する塩化水素などの酸性ガスを中和するための中和剤(消石灰等のアルカリ薬剤)と合わせて、ダイオキシン類等を吸着させる機能を有する吸着剤(活性炭等)が処理剤として集塵手段の上流側から供給される。これにより集塵手段において、塩化水素は中和剤により中和され、ダイオキシン類は吸着剤に吸着される。最終的には、塩化水素とダイオキシン類は、ばいじんとして回収されることにより、塩化水素とダイオキシン類の大気中への排出が抑えられる。 Based on the Act on Special Measures concerning Countermeasures against Dioxins, from December 1, 2002, emission standards for the concentration of dioxins in exhaust gas were imposed on all waste incineration systems according to the scale of the facility. In order to suppress the generation of harmful substances such as dioxins, measures such as suppressing the synthesis of dioxins are taken by maintaining a high temperature combustion state in each waste incineration system and promptly reducing the temperature after incineration. There is. In the unlikely event that dioxin is resynthesized in the temperature reduction process, it should be combined with a neutralizing agent (alkaline agent such as slaked lime) to neutralize acid gas such as hydrogen chloride generated by combustion. An adsorbent (activated carbon or the like) having a function of adsorbing dioxin or the like is supplied as a treatment agent from the upstream side of the dust collecting means. As a result, in the dust collecting means, hydrogen chloride is neutralized by the neutralizing agent, and dioxins are adsorbed by the adsorbent. Ultimately, hydrogen chloride and dioxins are recovered as soot and dust, so that the discharge of hydrogen chloride and dioxins into the atmosphere is suppressed.

通常、各廃棄物焼却システムでは予め焼却物の搬入基準値が設けられており、その範囲内においては、一定量の処理剤が常時供給されることで有害物質の発生が制御されている。ところが、予期せず想定外の焼却物が混入した場合には、処理剤の供給量を増やす必要がある。 Normally, each waste incineration system has a standard value for carrying in incineration in advance, and within that range, the generation of harmful substances is controlled by constantly supplying a certain amount of treatment agent. However, if an unexpected incinerated product is mixed in unexpectedly, it is necessary to increase the supply amount of the treatment agent.

この処理剤の供給量を調整するためには、排ガス中の有害物質を常時監視することが必要となる。例えば塩化水素については、レーザー式ガス分析計を用いて常時監視が可能であり、かつ精度よく検出できる。しかし、ダイオキシン類は微量物質であって常時直接的に検出することは困難である。
非特許文献1には、排ガス中のダイオキシン類の常時監視方法の例が記載されている。非特許文献1に示されているように、廃棄物焼却システムにおいて現在常時監視することが義務付けられている一酸化炭素及び塩化水素の濃度と、ダイオキシン類の濃度との間には高い相関は見られない。そのため、塩化ベンゼンや塩化フェノール等のダイオキシン類前駆物質の中で常時測定可能なものを分析機器を用いて測定するか、或いは、ダイオキシン類を2週間から1ヶ月間もの長期間サンプリングしてその試料を定量分析する方法などが開発され実用化されている。
In order to adjust the supply amount of this treatment agent, it is necessary to constantly monitor harmful substances in the exhaust gas. For example, hydrogen chloride can be constantly monitored using a laser gas analyzer and can be detected with high accuracy. However, dioxins are trace substances and it is difficult to detect them directly at all times.
Non-Patent Document 1 describes an example of a method for constantly monitoring dioxins in exhaust gas. As shown in Non-Patent Document 1, there is a high correlation between the concentrations of carbon monoxide and hydrogen chloride, which are currently required to be constantly monitored in waste incineration systems, and the concentrations of dioxins. I can't. Therefore, among dioxin precursors such as benzene chloride and phenol chloride, those that can be measured at all times are measured using an analytical instrument, or dioxins are sampled for a long period of 2 weeks to 1 month and the sample is used. A method for quantitative analysis of dioxins has been developed and put into practical use.

堀江宥治著、月刊資源環境対策2003年11月号「排ガス中のダイオキシン類常時監視-最近の測定技術動向とその活用について」Vol.39 No.13 p.120〜126Takafumi Horie, Monthly Resources and Environment Measures November 2003 issue "Constant monitoring of dioxins in exhaust gas-Recent measurement technology trends and their utilization" Vol. 39 No. 13 p. 120-126

しかしながら、非特許文献1に示されている技術では、直接的に前駆物質の常時測定が可能であってもガスクロマトグラフィーといった高価な分析機器が必要である。また、排ガス中のダイオキシン類の長期間サンプリングを行う方法でもダイオキシン類の平均濃度を確定するのに3週間程度を要するため、その間のダイオキシン類を監視することはできない。 However, the technique shown in Non-Patent Document 1 requires an expensive analytical instrument such as gas chromatography even if the precursor can be directly measured at all times. Further, even with the method of long-term sampling of dioxins in the exhaust gas, it takes about 3 weeks to determine the average concentration of dioxins, so it is not possible to monitor dioxins during that period.

本発明は、上記事情に鑑みなされたものであり、排ガス中のダイオキシン類の排出をより経済的且つ簡易に制御可能な廃棄物焼却システムを提供することを目的とする。 The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a waste incineration system capable of more economically and easily controlling the emission of dioxins in exhaust gas.

本発明者らの鋭意検討の結果、ダイオキシン類濃度は塩化水素濃度の測定値と相関を示さないが、塩化水素濃度の平均値と高い相関を示すとの知見が得られた。さらに、両者の間には、一定期間のタイムラグがあることが見出された。
かかる知見に基づいて提供される本発明の実施の形態に係る廃棄物焼却システムは、集塵手段と、該集塵手段の上流側に設けられた処理剤を供給する処理剤供給手段と、排ガス中の塩化水素濃度を連続的に測定する塩化水素濃度測定手段と、処理剤の供給を制御する処理剤供給制御手段と、を備える廃棄物焼却システムにおいて、処理剤は排ガス中のダイオキシン類を吸着させる機能を有する吸着剤を含み、処理剤供給制御手段は、塩化水素濃度の平均値に基づいて処理剤が増量される期間を制御することを特徴とするものである。
As a result of diligent studies by the present inventors, it was found that the dioxin concentration does not correlate with the measured value of the hydrogen chloride concentration, but shows a high correlation with the average value of the hydrogen chloride concentration. Furthermore, it was found that there was a time lag between the two.
The waste incineration system according to the embodiment of the present invention provided based on such knowledge includes a dust collecting means, a treatment agent supply means for supplying a treatment agent provided on the upstream side of the dust collecting means, and exhaust gas. In a waste incineration system including a hydrogen chloride concentration measuring means for continuously measuring the hydrogen chloride concentration in the waste incineration system and a treating agent supply controlling means for controlling the supply of the treating agent, the treating agent adsorbs dioxins in the exhaust gas. The treatment agent supply control means, which includes an adsorbent having a function of causing the treatment agent to be added, is characterized in that the period during which the treatment agent is increased is controlled based on the average value of the hydrogen chloride concentration.

また、処理剤供給制御手段は、平均値が塩化水素濃度の平均値上限を超えた場合に、処理剤を増量することを特徴とする。 Further, the treatment agent supply control means is characterized in that the amount of the treatment agent is increased when the average value exceeds the upper limit of the average value of the hydrogen chloride concentration.

また、処理剤が増量される期間は、前記平均値とダイオキシン類濃度とに基づき予め定められることを特徴とする。 Further, the period for increasing the amount of the treatment agent is predetermined based on the average value and the dioxin concentration.

処理剤が増量される期間は、平均値とダイオキシン類濃度との相関に基づき予め定められることを特徴とする。 The period for which the treatment agent is increased is characterized in that it is predetermined based on the correlation between the average value and the dioxin concentration.

相関は、平均値と排ガス中またはばいじん中の少なくとも一方のダイオキシン類濃度との相関に基づくものであることを特徴する。 The correlation is characterized by being based on the correlation between the mean value and the concentration of at least one dioxin in the exhaust gas or in soot and dust.

平均値は、30分以上3日以下の塩化水素濃度の測定データの平均値であることを特徴とする。 The average value is the average value of the measurement data of the hydrogen chloride concentration for 30 minutes or more and 3 days or less.

本発明によれば、排ガス中のダイオキシン類の排出をより簡易な手法で制御することが可能であり、ひいては排出される処理剤の量を削減可能な破棄物焼却システムを提供できる。 According to the present invention, it is possible to control the emission of dioxins in the exhaust gas by a simpler method, and it is possible to provide a waste incineration system capable of reducing the amount of the discharged treatment agent.

廃棄物焼却システムを表す概略図である。It is a schematic diagram which shows the waste incineration system. 吸着剤供給制御方法を示す図である。It is a figure which shows the adsorbent supply control method. 高塩素焼却物による排ガス中の塩化水素濃度への影響を示す図である。It is a figure which shows the influence on the hydrogen chloride concentration in exhaust gas by a high chlorine incineration product. 高塩素焼却物による塩化水素濃度平均値(1時間平均値)の挙動を示すグラフである。It is a graph which shows the behavior of the average value (1 hour average value) of hydrogen chloride concentration by a high chlorine incineration product. 排ガス中のダイオキシン類濃度と排ガス中の塩化水素濃度(24時間平均値)の相関を示す図である。(a)はダイオキシン類濃度と4日前の塩化水素濃度との相関を、(b)はダイオキシン類濃度と前日の塩化水素濃度との相関を示す。It is a figure which shows the correlation of the dioxin concentration in the exhaust gas and the hydrogen chloride concentration (24-hour average value) in the exhaust gas. (A) shows the correlation between the dioxin concentration and the hydrogen chloride concentration 4 days ago, and (b) shows the correlation between the dioxin concentration and the hydrogen chloride concentration the day before. ばいじん中のダイオキシン類濃度と排ガス中の塩化水素濃度(24時間平均値)の相関を示す図である。(a)はダイオキシン類濃度と4日前の塩化水素濃度との相関を、(b)はダイオキシン類濃度と前日の塩化水素濃度との相関を示す。It is a figure which shows the correlation of the dioxin concentration in soot and dust, and the hydrogen chloride concentration (24-hour average value) in exhaust gas. (A) shows the correlation between the dioxin concentration and the hydrogen chloride concentration 4 days ago, and (b) shows the correlation between the dioxin concentration and the hydrogen chloride concentration the day before. 排ガス中の塩化水素濃度(24時間平均値)と排ガス中及びばいじん中のダイオキシン類濃度との各相関係数の関係を示すグラフである。It is a graph which shows the relationship of each correlation coefficient between the hydrogen chloride concentration (24-hour average value) in exhaust gas, and the concentration of dioxins in exhaust gas and soot and dust. 排ガス中とばいじん中のダイオキシン類濃度の相関を示す図である。It is a figure which shows the correlation of the dioxin concentration in exhaust gas and soot and dust. 塩化水素濃度の平均値とダイオキシン類濃度(予測値)のタイムラグと吸着剤増量期間の関係を示すイメージ図である。It is an image diagram which shows the relationship between the time lag of the average value of hydrogen chloride concentration and the concentration of dioxins (predicted value), and the period of increasing the amount of adsorbent. 中和剤供給制御方法を示す図である。It is a figure which shows the neutralizing agent supply control method. ダイオキシン類抑制概念図である。It is a conceptual diagram of dioxin suppression.

本発明の一実施形態に関わる排ガス中のダイオキシン類を制御可能な廃棄物焼却システムの概要について図面を用いて説明する。 An outline of a waste incineration system capable of controlling dioxins in exhaust gas according to an embodiment of the present invention will be described with reference to the drawings.

図1は、本発明の一実施形態に係る廃棄物焼却システム10の系統を示す概略図である。なお、点線の矢印(図1中の11−6間、および6−7間)は排ガス処理手段による処理剤の供給およびばいじんの排出経路を示す。また、太矢印(図1中の12−20−11間)は、排ガス中の塩化水素濃度のデータを測定、演算処理し、処理剤供給装置11を制御する信号経路を示している。 FIG. 1 is a schematic view showing a system of a waste incineration system 10 according to an embodiment of the present invention. The dotted arrows (between 11-6 and 6-7 in FIG. 1) indicate the supply of the treatment agent and the discharge route of soot and dust by the exhaust gas treatment means. Further, a thick arrow (between 12 and 20-11 in FIG. 1) indicates a signal path for measuring and calculating the hydrogen chloride concentration data in the exhaust gas and controlling the processing agent supply device 11.

受入ホッパー1に投入される被焼却物については、通常、事前に高い塩素含有がないか確認されるが、実際の搬入時にも、サンプルを採取して高濃度の塩素含有がないか、確認することが求められる。もし、高塩素濃度が確認された場合には、当該被焼却物を受け入れない措置が取られる。但し、受入量が少なく全体の焼却処理量に対して影響が少ないと判断された場合はこの限りではない。 Normally, the incinerated material to be put into the receiving hopper 1 is checked in advance for high chlorine content, but even at the time of actual delivery, a sample is taken to check for high concentration chlorine content. Is required. If a high chlorine concentration is confirmed, measures will be taken not to accept the incinerated material. However, this does not apply if it is judged that the amount received is small and the total amount of incineration is not affected.

受入ホッパー1に投入された被焼却物は1次燃焼炉2に送られる。そして、1次燃焼炉2内のガス温度が850℃以上に保たれるとともに、一酸化炭素濃度瞬間測定値(5秒毎)が測定され、当該濃度が100ppm以下となるように運転管理することにより、ダイオキシン類の分解促進が図られる。なお、該一酸化炭素濃度の測定は1次燃焼炉2以降のいずれの場所において行われてもよく、例えば後述する煙突9において、塩化水素ガス濃度の測定と併せて行われても良い。
1次燃焼炉2から2次燃焼炉3は配管で接続されており、2次燃焼炉3の出口燃焼ガス温度も850℃以上を維持しながら配管により2次燃焼炉内のガスは廃熱ボイラー4に送られる。廃熱ボイラー4では、排ガスから熱を回収し、急冷塔(減温処理)5で190℃以下に急冷され、ダイオキシン類の再合成を防止する。
The incinerated material put into the receiving hopper 1 is sent to the primary combustion furnace 2. Then, the gas temperature in the primary combustion furnace 2 is maintained at 850 ° C. or higher, the instantaneous measurement value of carbon monoxide concentration (every 5 seconds) is measured, and the operation is controlled so that the concentration is 100 ppm or less. As a result, the decomposition of dioxin is promoted. The carbon monoxide concentration may be measured at any place after the primary combustion furnace 2, and may be measured together with the measurement of the hydrogen chloride gas concentration in the chimney 9 described later, for example.
The primary combustion furnace 2 to the secondary combustion furnace 3 are connected by a pipe, and the gas in the secondary combustion furnace is exhausted by the pipe while maintaining the outlet combustion gas temperature of the secondary combustion furnace 3 at 850 ° C. or higher. Sent to 4. In the waste heat boiler 4, heat is recovered from the exhaust gas and rapidly cooled to 190 ° C. or lower in the quenching tower (temperature reducing treatment) 5 to prevent the resynthesis of dioxins.

急冷塔5より排出されたガスは粉じんが含まれた状態で配管を通り、集塵機6の上流側に送られる。当該ガスには、塩化水素ガスの他、ダイオキシン類などの有害物質が再合成されるている可能性があるため、常時、集塵機6に取り付けられた処理剤供給装置11より、一定量処理剤が供給される。
処理剤としては、塩化水素ガス等の酸性ガス成分を中和させるためには、中和剤となるアルカリ薬剤(例えば、消石灰、重曹)が用いられるとともに、ダイオキシン類を吸着させるためには、吸着剤(例えば、活性炭、人工ゼオライト)を用いる。なお、本明細書では消石灰および活性炭を主に取り上げ記載するが、これらに限定されるものではない。
The gas discharged from the quenching tower 5 passes through the pipe in a state of containing dust and is sent to the upstream side of the dust collector 6. Since there is a possibility that harmful substances such as dioxins are resynthesized in the gas in addition to hydrogen chloride gas, a certain amount of the treatment agent is constantly added from the treatment agent supply device 11 attached to the dust collector 6. Be supplied.
As the treatment agent, an alkaline agent (for example, slaked lime, baking soda) as a neutralizing agent is used to neutralize the acid gas component such as hydrogen chloride gas, and is adsorbed to adsorb dioxin. Agents (eg, activated carbon, artificial zeolite) are used. In this specification, slaked lime and activated carbon are mainly taken up and described, but the present invention is not limited thereto.

処理剤としては、予め中和剤と吸着剤を所定の割合で混合したものを用いることができる。この場合、処理剤供給装置を1つとすることが可能となり、システムの簡素化を図ることができる。また、別の態様としては、中和剤と吸着剤を混合せずに用いることもできる。この場合、供給装置はそれぞれに対し必要となり2つとなるが、各供給量、供給期間、増量始期等を独立して管理できるというメリットを有する。特に、本発明は、塩化水素ガス濃度は中和剤投入により比較的短時間で低減するのに対し、ダイオキシン類濃度は塩化水素ガスが低減した後でも時間差をおいて増加する傾向があるという新たな知得に基づくものであり、両処理剤をそれぞれ有効なタイミング及び/又は期間、増量するように独立に制御し得ることは大きな効果を奏するものである。 As the treatment agent, a neutralizing agent and an adsorbent mixed in advance at a predetermined ratio can be used. In this case, it is possible to use only one treatment agent supply device, and the system can be simplified. Further, as another embodiment, the neutralizing agent and the adsorbent can be used without being mixed. In this case, two supply devices are required for each, but there is an advantage that each supply amount, supply period, start of increase, etc. can be managed independently. In particular, in the present invention, the hydrogen chloride gas concentration is reduced in a relatively short time by adding a neutralizing agent, whereas the dioxin concentration tends to increase with a time lag even after the hydrogen chloride gas is reduced. It is based on the knowledge, and it is very effective that both treatment agents can be independently controlled so as to increase the dose at an effective timing and / or period, respectively.

集塵機6においては、上流側から入った粉じんを含むガスがバグフィルターにより集塵ろ過される。粉じんは下流側に設けられたばいじん回収容器7に充填回収され、外部委託先によって処理される。集塵機6に送入されるガスの中には、硫黄酸化物、窒素酸化物、塩化水素等の酸性ガスが含まているが、これらは中和剤により中和され、またダイオキシン類などは吸着剤により吸着され、ばいじん回収容器7に充填回収される。 In the dust collector 6, the gas containing dust that has entered from the upstream side is dust-collected and filtered by the bag filter. The dust is filled and collected in a soot and dust collection container 7 provided on the downstream side, and is processed by an outsourcer. The gas sent to the dust collector 6 contains acid gases such as sulfur oxides, nitrogen oxides, and hydrogen chloride, which are neutralized by a neutralizing agent, and dioxin and the like are adsorbents. Is adsorbed by the gas, and is filled and collected in the dust collection container 7.

集塵機6で処理後のガスは、誘引送風機8により配管を通して煙突9に送られ系外に排出される。煙突9の中段には塩化水素ガス測定装置12が設置されており、塩化水素濃度の連続測定を行う。
なお、塩化水素ガス測定装置12の設置場所は煙突9に限られず、急冷塔(減温処理)5以降のいずれの場所に設置してもダイオキシン類発生量を予測する上で特段の支障はない。しかしながら、系外に排出される塩化水素ガスを測定するために設置される塩化水素ガス測定装置で取得されるデータを用いることがシステムの簡素化の面で好ましい。具体的には、処理剤による中和後の塩化水素ガス濃度を測定可能な集塵機以降(集塵機を含まない。)に塩化水素測定装置を設置することが好ましい。
The gas processed by the dust collector 6 is sent to the chimney 9 through a pipe by the attraction blower 8 and discharged to the outside of the system. A hydrogen chloride gas measuring device 12 is installed in the middle stage of the chimney 9 to continuously measure the hydrogen chloride concentration.
The location of the hydrogen chloride gas measuring device 12 is not limited to the chimney 9, and there is no particular problem in predicting the amount of dioxins generated regardless of the location after the quenching tower (temperature reduction treatment) 5. .. However, it is preferable from the viewpoint of simplification of the system to use the data acquired by the hydrogen chloride gas measuring device installed for measuring the hydrogen chloride gas discharged to the outside of the system. Specifically, it is preferable to install the hydrogen chloride measuring device after the dust collector (not including the dust collector) capable of measuring the hydrogen chloride gas concentration after neutralization with the treatment agent.

塩化水素ガス測定装置12は、従来の吸引式ガス濃度モニターよりも応答速度が最短で約2秒程度と高速であるだけでなく、サンプリング装置が不要で測定ポイントに直付け出来るため、リアルタイムでの濃度測定が可能なレーザー式ガス分析計であることが好ましい。
塩化水素ガス測定装置12では、常時、塩化水素濃度が所定の間隔で測定される。塩化水素ガス濃度は、例えば瞬間値として2秒毎に測定されるが、これに限られない。ただし、あまり測定間隔が短いとデータ取扱い上負荷が大きくなるので、1秒毎以上が好ましい。なお、瞬間値と測定値は基本的に同じものであるが、主に平均値に対応する用語として瞬間値という用語を用いている。
The hydrogen chloride gas measuring device 12 not only has a response speed as fast as about 2 seconds at the shortest than the conventional suction type gas concentration monitor, but also does not require a sampling device and can be directly attached to the measurement point, so that it can be directly attached to the measurement point in real time. A laser gas analyzer capable of measuring the concentration is preferable.
In the hydrogen chloride gas measuring device 12, the hydrogen chloride concentration is always measured at predetermined intervals. The hydrogen chloride gas concentration is measured every 2 seconds as an instantaneous value, for example, but is not limited to this. However, if the measurement interval is too short, the load on data handling becomes large, so every second or more is preferable. Although the instantaneous value and the measured value are basically the same, the term instantaneous value is mainly used as a term corresponding to the average value.

処理剤供給制御装置20は、塩化水素ガス測定装置12と処理剤供給装置11とを連動させる、内部に演算手段が具備された装置である。
処理剤供給制御装置20は、ダイオキシン類を抑制するために処理剤供給装置11から集塵機6に供給される吸着剤の量および供給期間を制御する機能と、塩化水素ガス等を抑制するために処理剤供給装置11から集塵機6に供給される中和剤の量および供給期間を制御する機能を有する。なお、処理剤供給装置11は、各機能に応じ個別に設けてもよいが、処理剤として混合剤を用いる場合は、ダイオキシン類または塩化水素ガスのどちらか一方に対し処理剤を混合して供給制御する。また、吸着剤および中和剤の各量は、重量、質量、供給速度等のいずれの単位、概念で規定してもよい。
以下、処理剤供給制御装置20の備える2つの機能について詳細に説明する。
The treatment agent supply control device 20 is a device provided with an internal calculation means that links the hydrogen chloride gas measuring device 12 and the treatment agent supply device 11.
The treatment agent supply control device 20 has a function of controlling the amount and supply period of the adsorbent supplied from the treatment agent supply device 11 to the dust collector 6 in order to suppress dioxins, and a treatment for suppressing hydrogen chloride gas and the like. It has a function of controlling the amount and supply period of the neutralizing agent supplied from the agent supply device 11 to the dust collector 6. The treatment agent supply device 11 may be provided individually according to each function, but when a mixture is used as the treatment agent, the treatment agent is mixed and supplied to either dioxins or hydrogen chloride gas. Control. Further, each amount of the adsorbent and the neutralizing agent may be specified by any unit or concept such as weight, mass, and supply rate.
Hereinafter, the two functions included in the processing agent supply control device 20 will be described in detail.

<処理剤供給制御装置20のダイオキシン類抑制機能>
はじめに、本発明の実施形態によるダイオキシン類抑制方法の概要を説明する。
本発明は、予め塩化水素濃度とダイオキシン類濃度を測定し、両者の相関から求められる増量期間を用いることにより、実際に業務として焼却処理を行う実運転(以下、「実運転」という。)時は塩化水素濃度の測定のみからダイオキシン類濃度の抑制を可能とするものである。図11の概念フローを参照し説明すると、実運転前に、予め塩化水素濃度とダイオキシン類濃度を事前測定する。このうち塩化水素濃度については平均化処理(平均値算出)を行い、平滑化された塩化水素濃度の経時変化を求める。そして、平滑化された塩化水素濃度とダイオキシン類濃度との相関処理を介して求められる増量期間を実運転時のための規定値として設定する。なお、増量期間の詳細については後述する。実運転時には増量期間を含む規定値を利用し、処理剤供給制御装置20により吸着剤量の制御を行うことで、実運転時に測定される塩化水素濃度のみからダイオキシン類の発生を抑制させることが可能となる。
<Dioxin suppression function of the treatment agent supply control device 20>
First, an outline of the method for suppressing dioxins according to the embodiment of the present invention will be described.
According to the present invention, the hydrogen chloride concentration and the dioxin concentration are measured in advance, and by using the increase period obtained from the correlation between the two, the incineration process is actually performed as a business (hereinafter referred to as "actual operation"). Makes it possible to suppress the concentration of dioxins only by measuring the concentration of hydrogen chloride. Explaining with reference to the conceptual flow of FIG. 11, the hydrogen chloride concentration and the dioxin concentration are measured in advance before the actual operation. Of these, the hydrogen chloride concentration is averaged (calculated as an average value) to determine the change over time in the smoothed hydrogen chloride concentration. Then, the increase period obtained through the correlation processing between the smoothed hydrogen chloride concentration and the dioxin concentration is set as a specified value for actual operation. The details of the increase period will be described later. By using the specified value including the increase period during actual operation and controlling the amount of adsorbent by the treatment agent supply control device 20, it is possible to suppress the generation of dioxins only from the hydrogen chloride concentration measured during actual operation. It will be possible.

続いて、実運転に際し処理剤供給制御装置20に予め格納しておく規定値ついて詳述する。
処理剤供給制御装置20には、吸着剤通常量、予め定めた塩化水素濃度測定値を平均化する期間(以下「平均化期間」という場合もある。)、吸着剤が増量される期間(以下「増量期間」という場合もある。)、予め設定した塩化水素濃度の平均値上限、増量される吸着剤の量の各情報が規定値として格納される。
Subsequently, the specified values stored in advance in the treatment agent supply control device 20 during the actual operation will be described in detail.
In the treatment agent supply control device 20, the normal amount of the adsorbent, the period for averaging the predetermined hydrogen chloride concentration measurement value (hereinafter, may be referred to as “average period”), and the period for increasing the amount of the adsorbent (hereinafter, hereinafter). Information on the "increase period"), the preset average upper limit of the hydrogen chloride concentration, and the amount of the adsorbent to be increased are stored as specified values.

吸着剤通常量とは、定常的に集塵機6に供給する吸着剤の量である。どのような廃棄物焼却場においても、ある程度の塩化水素ガスやダイオキシン類が発生する可能性があるので、予め一定量の吸着剤を常時供給することで、不測の事態に対処する。この量が多ければダイオキシン類の系外への散逸の危険性は下げられるが、一方で処理すべきばいじんの量が増大するため、コストの面で適当でない。よって、最適と考えられる量を予め設定しておく。吸着剤通常量は各焼却システムに依存する固有の値であるので、システムに応じ設定される。
なお、一定量の吸着剤を常時供給しない廃棄物焼却システムにおいては、吸着剤通常量は不要またはゼロに設定すれば良い。
The normal amount of the adsorbent is the amount of the adsorbent that is constantly supplied to the dust collector 6. Since a certain amount of hydrogen chloride gas and dioxins may be generated in any waste incinerator, a certain amount of adsorbent is always supplied in advance to deal with an unexpected situation. If this amount is large, the risk of dioxins dissipating out of the system can be reduced, but on the other hand, the amount of soot and dust to be treated increases, which is not appropriate in terms of cost. Therefore, the optimum amount is set in advance. Since the normal amount of the adsorbent is a unique value depending on each incineration system, it is set according to the system.
In a waste incineration system in which a fixed amount of adsorbent is not constantly supplied, the normal amount of adsorbent may be unnecessary or set to zero.

塩化水素濃度測定値を平均化する期間とは、測定された塩化水素濃度瞬間値の平均値を算出する際の平均化期間である。発明者らは、ダイオキシン類濃度と塩化水素濃度瞬間値との相関は低いが、平均値とは相関を示すことを見出した。これは、塩化水素濃度測定値は短時間での変動が激しいため、長周期変動を示すダイオキシン類濃度測定値とそのまま比較するには適していないことによると考えられる。
平均値を求めるための平均化期間は、短いと塩化水素濃度の短周期の影響が強く出てしまうため、少なくとも30分以上が好ましく、さらに好適には1時間以上が適している。また、あまり長いと良好な相関を得にくくなるため、少なくとも3日以下、好適には2日以下が適している。特に、実際の焼却作業のルーチン周期に合わせることが好ましく、例えば24時間ルーチンで焼却作業を行う場合においては、24時間平均が最適となる。例えば作業員が8時に交替する場合、前日の8時から当日の8時までの24時間平均値を使用する。あるいは、作業員の交替時間とは関係なく、前日の0から24時までの24時間平均値を使用しても良い。
なお、ダイオキシン類抑制対策のためだけであれば、塩化水素濃度の測定間隔を数秒とする必要はなく、例えば平均化期間に応じ10分程度とすることも可能である。
The period for averaging the measured hydrogen chloride concentration is the averaging period for calculating the average instantaneous value of the measured hydrogen chloride concentration. The inventors have found that the correlation between the dioxins concentration and the instantaneous value of hydrogen chloride concentration is low, but shows a correlation with the average value. It is considered that this is because the measured value of hydrogen chloride concentration fluctuates rapidly in a short period of time and is not suitable for comparison with the measured value of dioxin concentration showing long-period fluctuation.
If the averaging period for obtaining the average value is short, the influence of the short cycle of the hydrogen chloride concentration is strongly exerted. Therefore, at least 30 minutes or more is preferable, and 1 hour or more is more preferable. Further, if it is too long, it is difficult to obtain a good correlation, so that at least 3 days or less, preferably 2 days or less is suitable. In particular, it is preferable to match the routine cycle of the actual incineration work, and for example, when the incineration work is performed in a 24-hour routine, the 24-hour average is optimal. For example, when the worker changes at 8 o'clock, the 24-hour average value from 8 o'clock on the previous day to 8 o'clock on the current day is used. Alternatively, the 24-hour average value from 0 to 24:00 on the previous day may be used regardless of the worker shift time.
It should be noted that the measurement interval of the hydrogen chloride concentration does not need to be several seconds only for the measure of suppressing dioxins, and for example, it can be set to about 10 minutes depending on the averaging period.

次に吸着剤の増量期間について説明する。
本発明者の鋭意努力により、両パラメータ(ダイオキシン濃度と塩化水素濃度の平均値)の相関には数日間のタイムラグがあり、塩化水素濃度の平均値が高まった後にダイオキシン類濃度が上昇するとの知見が得られた。この理由は明らかではないが、一つの要因としてダイオキシンの再合成に数日間を要するものがあることが挙げられる。また、他の要因としては、配管や集塵機などに付着したダイオキシン類等が、数日後に剥離されている可能性も否定できない。いずれにしろ、このタイムラグを利用すれば、塩化水素濃度測定値(平均値)に基づき効果的にダイオキシン類の抑制を図ることが可能となる。よって、少なくともこのライムラグを上回る期間を吸着剤の増量期間として設定し、当該期間に亘、処理剤供給装置11から集塵機6に吸着剤を供給する。なお、このタイムラグは各廃棄物焼却システム固有の特性である可能性があるため、各廃棄物焼却システムにおいて予め求めておく。
具体的には、吸着剤の増量期間に関する情報を得るために、塩化水素ガス濃度とともに、煙突9から排出されるガスに含まれるダイオキシン類濃度または集塵機6の下流側のばいじん回収容器7により回収されるばいじんに含まれるダイオキシン類濃度の少なくとも一つを予め測定する(図11における「事前測定」)。なお、塩化水素濃度については、ダイオキシン類濃度の測定日より充分先行する形で測定することが肝要である。少なくとも5日前、好適には1週間以上前から塩化水素濃度を測定しておくことが望ましい。
次いで、設定した平均化期間ごとの塩化水素濃度の平均値を算出し、当該平均値の経時変化を求める(同図における「塩化水素濃度平均値算出」。続いて、時間関数としての平均値とダイオキシン類濃度測定値との相関を計算し(同図における「相関処理」)、両者間のタイムラグを求める。最後に、算出されたタイムラグに適宜安全率となる期間を加算し、吸着剤の増量期間とする。
Next, the period for increasing the amount of the adsorbent will be described.
It was found that due to the diligent efforts of the present inventor, there is a time lag of several days in the correlation between both parameters (mean value of dioxin concentration and hydrogen chloride concentration), and the dioxin concentration increases after the average value of hydrogen chloride concentration increases. was gotten. The reason for this is not clear, but one factor is that it takes several days to resynthesize dioxins. In addition, as another factor, it cannot be denied that dioxins and the like adhering to pipes and dust collectors may have been peeled off after a few days. In any case, if this time lag is used, it is possible to effectively suppress dioxins based on the measured value (average value) of hydrogen chloride concentration. Therefore, at least a period exceeding this lime lag is set as a period for increasing the amount of the adsorbent, and the adsorbent is supplied from the treatment agent supply device 11 to the dust collector 6 over the period. Since this time lag may be a characteristic peculiar to each waste incineration system, it is obtained in advance in each waste incineration system.
Specifically, in order to obtain information on the period for increasing the amount of the adsorbent, it is collected by the concentration of dioxins contained in the gas discharged from the chimney 9 or the dust collection container 7 on the downstream side of the dust collector 6 together with the concentration of hydrogen chloride gas. At least one of the dioxins concentration contained in the dust is measured in advance (“pre-measurement” in FIG. 11). It is important to measure the hydrogen chloride concentration sufficiently ahead of the measurement date of the dioxin concentration. It is desirable to measure the hydrogen chloride concentration at least 5 days before, preferably 1 week or more before.
Next, the average value of the hydrogen chloride concentration for each set averaging period is calculated, and the change with time of the average value is obtained (“calculation of the average value of hydrogen chloride concentration” in the figure. Then, the average value as a time function The correlation with the measured value of dioxin concentration is calculated (“correlation processing” in the figure), and the time lag between the two is calculated. Finally, the calculated time lag is appropriately added to the period for which the safety rate is obtained, and the amount of the adsorbent is increased. The period.

続いて、処理剤供給制御装置20によるダイオキシン類抑制機能の制御の流れを説明する。図2は制御の流れを示す一例であり、同図を参照しながら説明する。
処理剤供給制御装置20は、塩化水素ガス測定装置12で測定される塩化水素ガス濃度の平均値が上昇し、予め設定した塩化水素濃度の平均値上限を上回った場合に、自動的に処理剤供給装置11から集塵機6に投入される吸着剤が、予め設定した増量される吸着剤の量に応じ増量されるように処理剤供給装置11を制御する。なお、吸着剤を増量する方法としては、1回の投入量を増量する方法、投入頻度を増やす方法、あるいはそれらを組合わせた方法等、各種の運転条件の変更による方法がある。
吸着剤は、予め設定した吸着剤の増量期間が経過するまで増量状態を維持する(図2における「吸着剤増量処理」)。そして、増量期間経過後、測定された塩化水素濃度の平均値が平均値上限を下回ることが確認できた場合、吸着剤を減量する(図2における「吸着剤減量処理」)。例えば、減量量を増量量と同量とすることで、予め設定した吸着剤の通常量に戻るが、減量量を増量量より小さくすることで段階的に通常量に戻すことも可能である。
Subsequently, the flow of control of the dioxin suppression function by the treatment agent supply control device 20 will be described. FIG. 2 is an example showing the flow of control, and will be described with reference to FIG.
The treatment agent supply control device 20 automatically performs the treatment agent when the average value of the hydrogen chloride gas concentration measured by the hydrogen chloride gas measuring device 12 rises and exceeds the preset average value upper limit of the hydrogen chloride concentration. The processing agent supply device 11 is controlled so that the amount of the adsorbent charged from the supply device 11 into the dust collector 6 is increased according to the preset amount of the adsorbent to be increased. As a method of increasing the amount of the adsorbent, there are a method of increasing the amount of the adsorbent at one time, a method of increasing the frequency of the addition, a method of combining them, and a method of changing various operating conditions.
The adsorbent maintains the increased amount until the preset amount increasing period of the adsorbent elapses (“adsorbent increasing treatment” in FIG. 2). Then, when it is confirmed that the average value of the measured hydrogen chloride concentrations is below the upper limit of the average value after the elapse of the increase period, the amount of the adsorbent is reduced (“adsorbent reduction treatment” in FIG. 2). For example, by setting the weight loss amount to the same amount as the weight increase amount, the normal amount of the adsorbent set in advance is returned, but by making the weight loss amount smaller than the weight increase amount, it is possible to gradually return to the normal amount.

なお、吸着剤の増量期間中に再度、塩化水素ガス濃度の所定期間平均値が当該上限値を上回った場合に、その時点からさらに増量期間と同等の期間、処理剤の増量期間を延長させること、当該場合にさらに追加的増量を行うこと、これらを組み合わせること等は、安全サイドからみた場合に有効な一つの実施態様である。
これら平均値上限および増量される吸着剤の量は、任意の値とすることができ、例えば120ppmとすることが挙げられる。また、実際に高塩素濃度の焼却物を人為的に投入し、平均値上限や吸着剤の投入量を複数パターン変更する実験を試みることで、より適した値とするすることができる。
なお、処理剤供給制御装置20は、塩化水素ガス測定装置12または処理剤供給装置11と一体化した装置としてもよい。
If the average value of the hydrogen chloride gas concentration for a predetermined period exceeds the upper limit value again during the increase period of the adsorbent, the increase period of the treatment agent should be extended for a period equivalent to the increase period from that point. In that case, further increasing the amount, combining these, and the like are one effective embodiment from the viewpoint of safety.
The upper limit of these average values and the amount of the adsorbent to be increased can be any value, for example, 120 ppm. In addition, a more suitable value can be obtained by actually artificially adding an incinerated product having a high chlorine concentration and attempting an experiment in which the upper limit of the average value and the amount of the adsorbent added are changed in a plurality of patterns.
The treatment agent supply control device 20 may be a device integrated with the hydrogen chloride gas measuring device 12 or the treatment agent supply device 11.

<処理剤供給制御装置20の塩化水素濃度抑制機能>
処理剤供給制御装置20には、中和剤通常量、予め設けた塩化水素ガス濃度の瞬間値上限、中和剤増量量の各情報が格納される。
中和剤通常量は、定常的に集塵機6に供給する中和剤の量である。
予め設けた塩化水素ガス濃度の瞬間値上限は、各処理施設ごとに自主設定している塩化水素ガス濃度である。
中和剤増量量は、測定された塩化水素ガス濃度が塩化水素ガス濃度瞬間値上限を上回った際に増量される中和剤の量である。
ダイオキシン類抑制対策時と異なり、塩化水素ガスは中和剤との反応が速いため、塩化水素ガス濃度測定値が塩化水素ガス濃度瞬間値上限を上回ったことが確認され次第、中和剤を増量すれば、速やかに塩化水素ガスの低減を図ることができる。
また、中和剤増量状態の終期は、塩化水素ガス濃度の測定値が瞬間値上限を下回った時点と設定することに十分効果を奏することができる。図10に中和剤供給の制御方法の一態様をPAD図にて示す。
<Hydrogen chloride concentration suppression function of the treatment agent supply control device 20>
The treatment agent supply control device 20 stores information on the normal amount of the neutralizing agent, the upper limit of the instantaneous value of the hydrogen chloride gas concentration provided in advance, and the amount of the neutralizing agent increased.
The normal amount of the neutralizing agent is the amount of the neutralizing agent that is constantly supplied to the dust collector 6.
The upper limit of the instantaneous value of the hydrogen chloride gas concentration set in advance is the hydrogen chloride gas concentration voluntarily set for each treatment facility.
The amount of the neutralizing agent increased is the amount of the neutralizing agent that is increased when the measured hydrogen chloride gas concentration exceeds the upper limit of the instantaneous value of the hydrogen chloride gas concentration.
Unlike the measures to suppress dioxin, hydrogen chloride gas reacts quickly with the neutralizing agent, so the amount of neutralizing agent should be increased as soon as it is confirmed that the measured value of hydrogen chloride gas concentration exceeds the upper limit of the instantaneous value of hydrogen chloride gas concentration. If this is done, hydrogen chloride gas can be quickly reduced.
In addition, the final stage of the neutralizing agent increasing state can be sufficiently effective in setting the measured value of the hydrogen chloride gas concentration as the time when the measured value falls below the upper limit of the instantaneous value. FIG. 10 shows an aspect of the neutralizing agent supply control method in a PAD diagram.

また、当該瞬間値上限としては、ダイオキシン類抑制対策を目的とした塩化水素濃度の平均値上限と異なる値とすることも可能である。一般に平均値は、瞬間値のバラツキが平滑化されるため、瞬間値上限は平均値上限より高い値となる。 Further, the upper limit of the instantaneous value can be set to a value different from the upper limit of the average value of the hydrogen chloride concentration for the purpose of suppressing dioxins. In general, the upper limit of the instantaneous value is higher than the upper limit of the average value because the variation of the instantaneous value of the average value is smoothed.

以上を整理すると、塩化水素ガス抑制対策のためには、短周期の影響が残る塩化水素ガス濃度測定データ(瞬間値)に基づき、中和剤の増量始期、終期を定める。一方、ダイオキシン類抑制対策のためには、短周期の影響が除去されているデータ(平均値)に基づき、吸着剤剤の増量始期、終期を定める。特に、終期は塩化水素濃度平均値とダイオキシン類濃度との相関に基づき定めることを特徴とする。
なお、中和剤と吸着剤の混合された処理剤を用い、塩化水素ガス濃度およびダイオキシン類の両成分を抑制することを目的とする場合には、図2および図10に示した両制御方法を適宜組合わせれば良い。
Summarizing the above, in order to suppress hydrogen chloride gas, the start and end of increasing the amount of the neutralizing agent are determined based on the hydrogen chloride gas concentration measurement data (instantaneous value) that is affected by the short cycle. On the other hand, for measures to suppress dioxins, the start and end of increasing the amount of adsorbent are determined based on the data (mean value) from which the effects of short cycles are removed. In particular, the final stage is characterized in that it is determined based on the correlation between the average value of hydrogen chloride concentration and the concentration of dioxins.
When the purpose is to suppress both the hydrogen chloride gas concentration and the dioxins by using a treatment agent in which a neutralizing agent and an adsorbent are mixed, both control methods shown in FIGS. 2 and 10 are used. May be combined as appropriate.

以下、ダイオキシン類が再合成された場合でも、ダイオキシン類濃度が規定値を上回らないよう制御することが可能となる本発明の実施の形態に関わる廃棄物焼却システムついてさらに実施例に基づき説明する。 Hereinafter, the waste incineration system according to the embodiment of the present invention, which enables control of the dioxin concentration so as not to exceed a specified value even when dioxins are resynthesized, will be further described with reference to Examples.

はじめに本実施例で使用された廃棄物焼却システムで行われているダイオキシン類が発生する原因となる高塩素濃度焼却物の受け入れ制限について説明する。本実施例で使用した廃棄物焼却システムでは、高い塩素含有量の焼却物処理物を受け入れないよう被焼却物の全案件につき、受け入れ前の塩素含有量測定を可能な限り実施した。 First, the restrictions on the acceptance of high chlorine concentration incineration products that cause the generation of dioxins, which are carried out in the waste incineration system used in this example, will be described. In the waste incineration system used in this example, the chlorine content before acceptance was measured as much as possible for all the incinerated products so as not to accept the incinerated products having a high chlorine content.

本廃棄物焼却システムでは、受け入れ前と受け入れ時の2回、塩素濃度を調査した。受け入れ前は、排出事業者から情報提供してもらうか、事前に試料を提供してもらい塩素濃度を測定した。測定作業については、液状物と固形物により異なる。液状物については、pH試験紙で測定するが、油分などの影響でpH試験紙では測定不可能な場合は、油分を燃焼させて残った水分のpHを測定した。測定紙がpH3以下を示した場合は廃棄物焼却システムで処理する廃棄物としては塩素濃度が高すぎると判定し、原則受け入れ不可とした。固形物の場合、焼却物発生事業所等からの情報により塩素が含まれているか事前に情報提供をお願いした。塩素1wt%の場合には原則として受け入れ不可とした。但し、受入量が少なく全体の焼却処理量に対して影響が少ないと判断された場合は除いた。 In this waste incineration system, the chlorine concentration was investigated twice, before and at the time of acceptance. Before acceptance, the chlorine concentration was measured by having the discharger provide information or provide a sample in advance. The measurement work differs depending on whether it is a liquid or a solid. The liquid matter is measured with a pH test paper, but when it is not possible to measure with the pH test paper due to the influence of oil or the like, the pH of the water remaining after burning the oil is measured. If the measurement paper shows a pH of 3 or less, it is judged that the chlorine concentration is too high for the waste to be treated by the waste incineration system, and it is not accepted in principle. In the case of solids, we requested that information be provided in advance to see if chlorine is contained based on information from the incineration plant. In principle, 1 wt% chlorine was unacceptable. However, this was excluded when it was judged that the amount received was small and the total amount of incineration was not affected.

本実施例では、図1に記載された廃棄物焼却システムを用いた。ただし、本実施例における処理剤供給量は一定とし、実験途中で処理剤の増量、減量は行わなかった。また、焼却処理物の焼却は、焼却処理工程の1次燃焼炉2では炉内燃焼ガス温度を850℃以上に保ち、2次燃焼炉3までの出入口温度も850℃以上に維持するように行うとともに、滞留時間を2秒以上確保させた。
各燃焼炉の燃焼ガス温度を確認した結果、2次燃焼炉3出口まではダイオキシン類は生成されないと考えられ、さらに過熱残渣を分析した結果、全て検出限界以下であり無害化されていることを確認できた。また二次燃焼炉内のライニング及び付着物についても調査したが、ダイオキシン類及び塩素は検出限界以下であった。
In this embodiment, the waste incineration system shown in FIG. 1 was used. However, the amount of the treatment agent supplied in this example was kept constant, and the amount of the treatment agent was not increased or decreased during the experiment. Further, the incineration of the incinerated product is carried out so that the combustion gas temperature in the furnace is maintained at 850 ° C. or higher in the primary combustion furnace 2 in the incineration treatment step, and the inlet / outlet temperature up to the secondary combustion furnace 3 is also maintained at 850 ° C. or higher. At the same time, the residence time was secured for 2 seconds or more.
As a result of checking the combustion gas temperature of each combustion furnace, it is considered that dioxins are not generated up to the 3 outlets of the secondary combustion furnace, and as a result of further analysis of the superheat residue, it is found that all of them are below the detection limit and are detoxified. It could be confirmed. The lining and deposits in the secondary combustion furnace were also investigated, but dioxins and chlorine were below the detection limit.

調査結果からダイオキシン類は、廃熱ボイラー4から急冷塔5までの減温処理工程付近にて再合成されると推定された。 From the survey results, it was estimated that dioxins are resynthesized near the temperature reduction treatment process from the waste heat boiler 4 to the quenching tower 5.

廃棄物焼却システムに投入された高塩素焼却物由来の塩化水素ガスは、集塵機6の誘因送風機8を通して排出されるガスを煙突9中段の塩化水素ガス測定装置12により常時監視した。ここでは京都電子製レーザー式ガス分析計(型式名KLA)を使用し、瞬間値の測定間隔は2秒に設定した。 Regarding the hydrogen chloride gas derived from the high chlorine incineration material introduced into the waste incineration system, the gas discharged through the incentive blower 8 of the dust collector 6 was constantly monitored by the hydrogen chloride gas measuring device 12 in the middle stage of the chimney 9. Here, a laser gas analyzer (model name KLA) manufactured by Kyoto Electronics was used, and the measurement interval of the instantaneous value was set to 2 seconds.

処理剤には、秩父石灰工業株式会社の高反応性消石灰(活性炭15%配合)、平均粒径8μm、BET45m2/g、細孔容積0.2cm2/g、CaO≧72.5%を用いた。当該処理剤は塩化水素及びダイオキシン類を抑制する性能を有する。 As the treatment agent, highly reactive slaked lime (containing 15% activated carbon) of Chichibu Lime Industry Co., Ltd., an average particle size of 8 μm, a BET of 45 m2 / g, a pore volume of 0.2 cm2 / g, and CaO ≧ 72.5% were used. The treatment agent has the ability to suppress hydrogen chloride and dioxins.

供給される処理剤の量は、2.4kg/hとした。この内、消石灰供給量は2.0kg/h、活性炭は0.4kg/hであった。この時の排ガス中の塩化水素は100ppm程度、二酸化硫黄は15ppm程度で推移した。投入された消石灰がすべて反応していたものと仮定すると、投入された汚泥に起因する塩化水素は177ppmと推定された。 The amount of the treatment agent supplied was 2.4 kg / h. Of these, the amount of slaked lime supplied was 2.0 kg / h and that of activated carbon was 0.4 kg / h. At this time, hydrogen chloride in the exhaust gas remained at about 100 ppm, and sulfur dioxide remained at about 15 ppm. Assuming that all the slaked lime added had reacted, the amount of hydrogen chloride caused by the added sludge was estimated to be 177 ppm.

本実施例では、高塩素焼却物として、塩素を4〜5%程度含むと考えられる汚泥を午前8:00〜11:00、午後01:00〜4:00の2回投入し、意図的に排ガスの塩化水素濃度を高め、処理剤供給制御装置20および処理剤供給装置11が、自主設定した塩化水素濃度瞬間値上限200ppmを超えた場合に的確に作動するか検証した。 In this embodiment, sludge, which is considered to contain about 4 to 5% of chlorine, is intentionally added as a high-chlorine incinerator twice, from 8:00 am to 11:00 am and from 01:00 pm to 4:00 pm. The hydrogen chloride concentration of the exhaust gas was increased, and it was verified whether the treatment agent supply control device 20 and the treatment agent supply device 11 operate properly when the voluntarily set upper limit of the instantaneous value of hydrogen chloride concentration of 200 ppm is exceeded.

処理剤供給装置11はゲートバルブ及び電動ロータリーバルブにより供給量制御を行っている。本実施例では、予め検証されていた通常運転時の4秒運転-60秒停止の間欠運転を基本としとしていたが、処理剤供給制御装置20が塩化水素濃度が塩化水素濃度瞬間値上限の超過を検知すると運転条件が切り替えられ、16秒運転−30秒停止の間欠運転に変更される設定とした。 The processing agent supply device 11 controls the supply amount by a gate valve and an electric rotary valve. In this embodiment, the basic operation was the intermittent operation of 4-second operation-60-second stop during normal operation, which had been verified in advance, but the treatment agent supply control device 20 exceeded the upper limit of the instantaneous value of hydrogen chloride concentration in the treatment agent supply control device 20. When is detected, the operating conditions are switched, and the setting is changed to intermittent operation for 16 seconds operation and 30 seconds stop.

図3に塩化水素濃度の経時変化を示す。図3の通り、午前中の塩素を含む汚泥投入開始後、30分後には排ガス中の塩化水素濃度が上昇を始め200ppmを超えると、処理剤供給制御装置20が処理剤供給装置11を制御し処理剤が増加供給され、数秒後には200ppm以下となった。この動作は3回発生した。午後は午前中とは異なり、塩素を含む汚泥投入開始後1時間30分を過ぎてから塩化水素濃度が上昇し、計19回200ppm以上を検知したが、処理剤増量供給効果により、いずれも45秒以内には200ppm以下となる挙動を繰り返した。したがって、塩化水素濃度の上昇に対して、当該処理剤供給制御装置20および処理剤供給装置11で対応可能であることが確認できた。 FIG. 3 shows the change over time in the hydrogen chloride concentration. As shown in FIG. 3, the treatment agent supply control device 20 controls the treatment agent supply device 11 when the hydrogen chloride concentration in the exhaust gas starts to increase and exceeds 200 ppm 30 minutes after the start of sludge injection containing chlorine in the morning. The treatment agent was additionally supplied, and after a few seconds, it became 200 ppm or less. This operation occurred three times. In the afternoon, unlike in the morning, the hydrogen chloride concentration increased 19 times in total 19 times or more after 1 hour and 30 minutes after the start of sludge containing chlorine, but due to the effect of increasing the amount of treatment agent, all 45 Within seconds, the behavior of 200 ppm or less was repeated. Therefore, it was confirmed that the treatment agent supply control device 20 and the treatment agent supply device 11 can cope with the increase in the hydrogen chloride concentration.

図3の2秒ごとの瞬間値データを図4のように1時間ごとの平均値とすると当該処理剤の効果を容易に確認できる。したがって、1時間平均値を監視することで排ガス中の塩化水素濃度を監視制御することも可能である。但し、瞬間値を平滑化した値であるため、上限値は瞬間値よりも低く、例えば120ppmとすることが望ましい。 When the instantaneous value data every 2 seconds in FIG. 3 is taken as the average value every hour as shown in FIG. 4, the effect of the treatment agent can be easily confirmed. Therefore, it is also possible to monitor and control the hydrogen chloride concentration in the exhaust gas by monitoring the 1-hour average value. However, since the instantaneous value is a smoothed value, the upper limit value is lower than the instantaneous value, and is preferably 120 ppm, for example.

また本実施例では、排ガス中のダイオキシン類濃度とばいじん中のダイオキシン類濃度の測定を計7回行った。測定は外部分析機関により、排ガス中のダイオキシン類濃度の測定はJISK0311「排ガス中のダイオキシン類の測定方法」に従い、ばいじん中のダイオキシン類濃度の測定は、ダイオキシン類対策特別措置施行規則第二条二項第一号の規定に基づき環境大臣が定める方法を用いて行われた。 Further, in this example, the concentration of dioxins in the exhaust gas and the concentration of dioxins in the soot and dust were measured 7 times in total. The measurement is performed by an external analysis organization, and the measurement of the concentration of dioxins in the exhaust gas is in accordance with JIS K0311 "Measurement method of the dioxins in the exhaust gas". It was carried out using the method specified by the Minister of the Environment based on the provisions of Item 1.

次いで、排ガス及びばいじん中のダイオキシン類測定値と、塩化水素濃度の24時間平均値との相関係数Rを求めた。なお、塩化水素濃度の24時間平均値は前日の平均値から5日前の平均値までの5種類の平均値を求め、各平均値に対し、ダイオキシン類測定値との相関係数Rを求めた。この結果を表1に纏めるとともに、排ガス中のダイオキシン類測定値と前日および4日前の塩化水素濃度平均値との相関係数の関係を示すグラフを図5に、ばいじん中のダイオキシン類測定値と前日および4日前の塩化水素濃度平均値との相関係数の関係を示すグラフを図6に示した。 Next, the correlation coefficient R between the measured values of dioxins in the exhaust gas and soot and dust and the 24-hour average value of the hydrogen chloride concentration was determined. For the 24-hour average value of hydrogen chloride concentration, five kinds of average values from the average value of the previous day to the average value of 5 days ago were obtained, and the correlation coefficient R with the measured value of dioxins was obtained for each average value. .. The results are summarized in Table 1, and a graph showing the relationship between the measured values of dioxin in the exhaust gas and the correlation coefficient between the average values of hydrogen chloride concentrations on the previous day and 4 days ago is shown in Fig. 5 with the measured values of dioxin in soot and dust. FIG. 6 shows a graph showing the relationship of the correlation coefficient with the average value of hydrogen chloride concentration on the previous day and 4 days ago.

Figure 2020179353
Figure 2020179353

また、表1のデータを用い、横軸を日にち、縦軸を相関係数Rとしてダイオキシン類濃度と塩化水素濃度平均値との関係をグラフにすると、図7のように4日前をピークに高い相関が見られるが、5日前には測定日前日程度の相関係数Rになることが分かった。すわなち、排ガス中のダイオキシン類濃度と24時間平均化後の塩化水素濃度の相関には4日間のタイムラグあることを確認した。そこで、処理剤の増量期間は少なくとも4日以上、安全率を考慮し、5日以上とした。なお、このタイムラグは各廃棄物焼却システムに依存する値であるので、各システムごとに予め求めておく必要がある。
また、ダイオキシン類濃度と塩化水素濃度との相関関係は、排ガス中およびばいじん中のいずれのダイオキシン類濃度においても同様に認められた。排ガス中とばいじん中の両者のダイオキシン類濃度の相関は、図8に示すように高いものであった(相関係数R=0.8911)。
Using the data in Table 1, the horizontal axis is the date and the vertical axis is the correlation coefficient R. When the relationship between the dioxin concentration and the average value of hydrogen chloride concentration is graphed, the peak is high 4 days ago as shown in FIG. A correlation can be seen, but it was found that the correlation coefficient R was about 5 days before the measurement day. That is, it was confirmed that there was a time lag of 4 days in the correlation between the concentration of dioxins in the exhaust gas and the concentration of hydrogen chloride after averaging for 24 hours. Therefore, the period for increasing the amount of the treatment agent was set to at least 4 days or more, and 5 days or more in consideration of the safety factor. Since this time lag is a value that depends on each waste incineration system, it is necessary to obtain it in advance for each system.
Moreover, the correlation between the dioxin concentration and the hydrogen chloride concentration was similarly observed in both the dioxin concentration in the exhaust gas and the soot and dust. The correlation between the concentrations of dioxins in the exhaust gas and in the soot and dust was high as shown in FIG. 8 (correlation coefficient R = 0.8911).

これらの結果より、塩化水素濃度に基づきダイオキシン濃度の抑制対策を行うための情報(相関に基づく情報)を得るためには、排ガス中のダイオキシン類濃度測定値でも、ばいじん中のダイオキシン類濃度測定値でも用いることができるとの知見が得られた。 From these results, in order to obtain information (information based on correlation) for taking measures to suppress dioxin concentration based on hydrogen chloride concentration, even the dioxin concentration measurement value in exhaust gas is the dioxin concentration measurement value in soot and dust. However, it was found that it can be used.

今回の実験に使用した廃棄物焼却システムにおいては、通常操業時、処理剤2.4kg/h(消石灰に活性炭を15%配合した中和剤と吸着剤の混合剤)を供給して塩化水素濃度を常時監視したが、前述の予め行った相関関係に基づくタイムラグ情報の結果に基づき、前日0時から24時までの塩化水素濃度24時間平均値が事前に設定した平均値上限(例えば120ppm)を超過したことを確認した日から、タイムラグを考慮して相関関係がなくなると予測される5日後まで処理剤の増量を維持した。尚、瞬間値として2秒毎の塩化水素濃度の測定データが瞬間値上限200ppmを超えた場合については別途自動的に処理剤を増量するシステムとすることで、塩化水素濃度の上昇にも対応することができた。 In the waste incineration system used in this experiment, during normal operation, a treatment agent of 2.4 kg / h (a mixture of a neutralizer containing 15% activated carbon in slaked lime and an adsorbent) was supplied to concentrate hydrogen chloride. Was constantly monitored, but based on the result of the time lag information based on the correlation performed in advance, the 24-hour average value of hydrogen chloride concentration from 0:00 to 24:00 on the previous day was set to the preset average upper limit (for example, 120 ppm). The dose of the treatment agent was maintained from the day when the excess was confirmed to 5 days after the correlation was expected to disappear in consideration of the time lag. If the measurement data of hydrogen chloride concentration every 2 seconds exceeds the upper limit of 200 ppm as an instantaneous value, the system automatically increases the amount of the treatment agent to cope with the increase in hydrogen chloride concentration. I was able to.

排ガス中の塩化水素濃度の平均値が平均値上限を超えた後、上昇すると予測されるダイオキシン類濃度のタイムラグをイメージ化すると図9のようになる。塩化水素濃度の瞬間値が上限値を超えた時点であって、まだ塩化水素濃度平均値が平均値上限を超えていない時点Aでは、消石灰など酸性ガス成分を中和させる中和剤が直ちに増量される。また塩化水素濃度の平均値が平均値上限を超えた時点Bで、ダイオキシン類等を吸着させるための吸着剤を増量する。そして、イメージではあるがダイオキシン類濃度と塩化水素濃度平均値の相関関係がなくなる時点C(本実施例では5日後)まで供給を継続する。 FIG. 9 shows an image of the time lag of the concentration of dioxins, which is predicted to increase after the average value of the hydrogen chloride concentration in the exhaust gas exceeds the upper limit of the average value. At the time when the instantaneous value of hydrogen chloride concentration exceeds the upper limit and the average value of hydrogen chloride concentration does not exceed the upper limit of the average value A, the amount of neutralizing agent that neutralizes acid gas components such as slaked lime is immediately increased. Will be done. Further, at the time point B when the average value of the hydrogen chloride concentration exceeds the upper limit of the average value, the amount of the adsorbent for adsorbing dioxins and the like is increased. Then, although it is an image, the supply is continued until the time point C (5 days later in this example) when the correlation between the dioxin concentration and the average value of the hydrogen chloride concentration disappears.

我が国においてはダイオキシン類の排出規制に伴い、基準を満たせない既設炉には高度処理技術を備えた焼却設備および排ガスの処理設備が設置され、排出基準値が達成されているが、その投資額は廃棄物焼却システムを有する廃棄物処分事業者にとって大きな負担となっている。本廃棄物焼却システムによれば、導入費用および維持費用を安く抑えれるとともに、排出される処理剤の量を削減できるので、専用の廃棄物焼却施設のみならず、ダイオキシン類の発生が予想される生産システムの一部としても利用可能である。 In Japan, due to the emission regulations for dioxins, incineration equipment equipped with advanced treatment technology and exhaust gas treatment equipment have been installed in existing furnaces that do not meet the standards, and the emission standard values have been achieved, but the investment amount is It is a heavy burden for waste disposal companies that have a waste incineration system. According to this waste incineration system, the introduction cost and maintenance cost can be kept low, and the amount of waste treatment agent can be reduced. Therefore, not only the dedicated waste incineration facility but also dioxins are expected to be generated. It can also be used as part of a production system.

1・・・受入ホッパー、2・・・1次燃焼炉、3・・・2次燃焼炉、4・・・廃熱ボイラー、5・・・急冷塔(減温処理)、6・・・集塵機、7・・・ばいじん回収容器 8・・・誘引送風機、9・・・煙突、10・・・廃棄物焼却システム全体、11・・・処理剤供給装置、12・・・塩化水素ガス測定装置、20・・・処理剤供給制御装置 1 ... Receiving hopper, 2 ... Primary combustion furnace, 3 ... Secondary combustion furnace, 4 ... Waste heat boiler, 5 ... Quench cooling tower (temperature reduction treatment), 6 ... Dust collector , 7 ... soot and dust collection container 8 ... attraction blower, 9 ... chimney, 10 ... entire waste incineration system, 11 ... treatment agent supply device, 12 ... hydrogen chloride gas measuring device, 20 ... Treatment agent supply control device

Claims (6)

集塵手段と、該集塵手段の上流側に設けられた処理剤を供給する処理剤供給手段と、排ガス中の塩化水素濃度を連続的に測定する塩化水素濃度測定手段と、前記処理剤の供給を制御する処理剤供給制御手段と、を備える廃棄物焼却システムにおいて、
前記処理剤は前記排ガス中のダイオキシン類を吸着させる機能を有する吸着剤を含み
前記処理剤供給制御手段は、前記塩化水素濃度の平均値に基づいて前記処理剤が増量される期間を制御することを特徴とする廃棄物焼却システム。
A dust collecting means, a treatment agent supply means for supplying a treatment agent provided on the upstream side of the dust collecting means, a hydrogen chloride concentration measuring means for continuously measuring the hydrogen chloride concentration in exhaust gas, and the treatment agent. In a waste incineration system including a treatment agent supply control means for controlling supply.
The treatment agent includes an adsorbent having a function of adsorbing dioxins in the exhaust gas, and the treatment agent supply control means controls the period during which the treatment agent is increased based on the average value of the hydrogen chloride concentration. A waste incineration system featuring.
前記処理剤供給制御手段は、前記平均値が塩化水素濃度の平均値上限を超えた場合に、前記処理剤を増量することを特徴とする請求項1記載の廃棄物焼却システム。 The waste incineration system according to claim 1, wherein the treatment agent supply control means increases the amount of the treatment agent when the average value exceeds the upper limit of the average value of the hydrogen chloride concentration. 前記処理剤が増量される期間は、前記平均値とダイオキシン類濃度とに基づき予め定められることを特徴とする請求項1および請求項2記載の廃棄物焼却システム。 The waste incineration system according to claim 1 and 2, wherein the period for increasing the amount of the treatment agent is predetermined based on the average value and the dioxin concentration. 前記処理剤が増量される期間は、前記平均値とダイオキシン類濃度との相関に基づき予め定められることを特徴とする請求項1乃至請求項3記載の廃棄物焼却システム。 The waste incineration system according to claim 1 to 3, wherein the period for increasing the amount of the treatment agent is predetermined based on the correlation between the average value and the dioxin concentration. 前記相関は、前記平均値と排ガス中またはばいじん中の少なくとも一方のダイオキシン類濃度との相関に基づくものであることを特徴する請求項4記載の廃棄物焼却システム。 The waste incineration system according to claim 4, wherein the correlation is based on a correlation between the mean value and the concentration of at least one dioxin in exhaust gas or soot and dust. 前記平均値は、30分以上3日以下の塩化水素濃度の測定データの平均値であることを特徴とする請求項1乃至請求項5記載の廃棄物焼却システム。 The waste incineration system according to claim 1 to 5, wherein the average value is an average value of measurement data of hydrogen chloride concentration of 30 minutes or more and 3 days or less.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09308817A (en) * 1996-05-22 1997-12-02 Babcock Hitachi Kk Method for treating exhaust gas and apparatus therefor
JP2000317264A (en) * 1999-05-17 2000-11-21 Nkk Corp Method for removing harmful component in waste gas and device for treating waste gas
JP2001208744A (en) * 2000-01-28 2001-08-03 Hitachi Ltd Dioxin concentration evaluating method
JP2005199198A (en) * 2004-01-16 2005-07-28 Takuma Co Ltd Method for controlling exhaust gas treatment facility
JP2007237019A (en) * 2006-03-06 2007-09-20 Mitsui Eng & Shipbuild Co Ltd Feed amount control method for exhaust gas treatment chemical and exhaust gas treatment apparatus

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09308817A (en) * 1996-05-22 1997-12-02 Babcock Hitachi Kk Method for treating exhaust gas and apparatus therefor
JP2000317264A (en) * 1999-05-17 2000-11-21 Nkk Corp Method for removing harmful component in waste gas and device for treating waste gas
JP2001208744A (en) * 2000-01-28 2001-08-03 Hitachi Ltd Dioxin concentration evaluating method
JP2005199198A (en) * 2004-01-16 2005-07-28 Takuma Co Ltd Method for controlling exhaust gas treatment facility
JP2007237019A (en) * 2006-03-06 2007-09-20 Mitsui Eng & Shipbuild Co Ltd Feed amount control method for exhaust gas treatment chemical and exhaust gas treatment apparatus

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