JP2003175372A - Soil manufacturing method, soil treatment apparatus, treatment method and treatment apparatus - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a soil manufacturing method for manufacturing clean soil from soil polluted with an organohalogen compound such as dioxins or the like, and a soil treatment apparatus. <P>SOLUTION: Matter to be treated such as soil, incineration ash or the like containing the organohalogen compound is introduced into a hermetically closable pyrolytic furnace 310 to be heated under reduced pressure. The gaseous discharged matter of the matter to be treated is treated so as to suppress the formation and re-synthesis of dioxins. The heated residue of the matter to be treated is purged with a substitution gas free from the organohalogen compound or having organohalogen compound forming capacity before cooled. By this method, the concentration of the organohalogen compound remaining in the heated residue of the matter to be treated can be suppressed to an extremely low level. <P>COPYRIGHT: (C)2003,JPO

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a treatment method and a treatment apparatus capable of suppressing the generation of dioxin,
In particular, the present invention relates to a treatment device and a treatment method capable of suppressing the thermal decomposition treatment of abandoned vehicles and the like, the generation of dust from factories, general households, etc., and the generation of organic halides containing dioxin in the treatment of waste. The present invention also relates to a treatment method and a treatment device capable of reducing the residual dioxin concentration in a thermal decomposition residue, an incineration residue, a residual liquid, soil, sludge, etc., containing a harmful organic halide such as dioxin. The invention further relates to a method for producing clean soil from soil containing organic halides such as dioxins.

[0002]

2. Description of the Related Art Recently, as the number of vehicles such as passenger cars, buses, trucks, etc. produced has increased, the number of vehicles to be disposed of has also increased significantly, and garbage such as households and factories, household appliances, etc. The amount of such substances has also increased, and new pollution has been pointed out with the disposal of such substances. That is, these junk cars, scraps, garbage, shredders contain various substances such as iron, non-ferrous metals, plastics and rubbers, and when these substances are pyrolyzed or incinerated, NOx, SO
x, or harmful organic halides such as dioxins are generated. Then, a large amount thereof remains in the heating residue such as the thermal decomposition residue and the incineration residue, or in the gaseous emission, the liquid emission, and the residual liquid due to the incineration and thermal decomposition. Dioxins are extremely poisonous and their adverse effects on the human body are reported every day. In fact, incineration fly ash, thermal decomposition residue, incineration waste gas,
Organic halides such as dioxins remain in the residual liquid and further in soot and dust, which is a big social problem.

Therefore, as measures against this dioxins, various studies have been conducted on the suppression of the generation of dioxins and the safe and effective detoxification treatment of dioxins. However, until now, it cannot be said that an effective treatment technique for organic halides containing dioxins has been established.

Objects to be treated containing incineration fly ash, soil, sludge, dioxins such as agricultural products and marine products, and harmful organic halides such as PCB and coplanar PCB, or
It is known that when an object to be treated that can generate organic halides such as household waste, shredder dust, and circuit boards is heated in a reducing atmosphere, a dechlorination reaction occurs, which is effective in reducing the concentration of dioxins. ing. It is generally known that dioxins are decomposed by heating at about 500 ° C. or higher in a reducing atmosphere. Therefore, if the object to be treated is heated while maintaining the system in a reducing atmosphere, dioxins can be decomposed. However, whether incinerated or pyrolyzed, it is inevitable that dioxin will be produced in the heating process from room temperature to about 500 ° C, and effective measures against dioxins generated in this heating process have not yet been taken. Not established. Therefore, it is required to establish an effective treatment technique for dioxins generated in the process of reaching a predetermined heating temperature of the object to be treated. Further, when the steaming treatment (pyrolysis treatment) of the object to be treated containing an organic halide or the object to be treated which can generate an organic halide as described above is carried out according to the conventional dioxin countermeasure, a predetermined vacuum is applied to the inside of the heating chamber. However, there is a problem that it is difficult to hold the temperature once and raise the temperature to a predetermined temperature all at once.

Diffusion of organic halides such as dioxins, PCBs and coplanar PCBs into the environment and their effects have become a serious social problem. For example, harmful organic halides such as dioxins remain in the heating residues (ash, char, carbon) obtained by burning and pyrolyzing waste. Further, for example, high concentrations of dioxins have been detected in the soil around the refuse incineration plant and the industrial waste disposal site, and there is a serious concern about the adverse effects on the health of the residents. Soil and sludge also contain organic halides.

[0006] As described above, in many cases, residues of organic waste such as dioxins, or heavy metals remain in the heating residue of waste, solids such as soil and sludge under special conditions, and liquids.

As a method for removing harmful substances containing these organic halides or heavy metals, the object to be treated containing the organic halide is heated to a high temperature, or about 1500
A method has been proposed in which the concentration of the organic halide is reduced by performing a melting process at a high temperature of about ° C. However, such a method has problems that an expensive and large-scale facility is required, running cost is high, and the like. Further, there is a problem that it is not possible to deal with dioxins generated during the period from room temperature to the decomposition temperature of dioxins. Organic halides such as dioxins around the incineration facility, As, Hg, Cd, Pb,
No effective treatment technology has been established for soil or the like that has been flooded with Cr ^{+6 and the} like.

In the case of treating municipal wastes by burning (incineration) or the like, the production of organic halides can be reduced if they can be completely burned. However, it is very difficult to completely burn a large amount of non-uniform object to be treated. Even if complete combustion is possible, harmful organic halides such as dioxins will be produced before reaching a predetermined temperature.

Organic halides such as dioxins remain in the heating residue which is the residue of the heat treatment of the object to be treated such as incineration and thermal decomposition, and the concentration of the organic halide remaining in the heating residue is reduced and removed. It is required to establish heat treatment technology.

By the way, in order to generate dioxin, a reactive chlorine atom that bonds with the carbon of the benzene nucleus,
The presence of oxygen that binds the benzene nucleus is required (see Figure 6). Figure 6 shows Choudrey in the United States.
It is the flow of the chemical reaction at the time of incineration estimated by hry) et al.
In order to suppress the production of dioxins during thermal decomposition, it is considered effective to control the amounts of these reactive chlorine atoms and oxygen in the thermal decomposition furnace. However, a thermal decomposition furnace suitable for preventing the generation of dioxins has not been proposed from such a viewpoint. In particular, suppression of formation of organic halides such as dioxins and coplanar PCB at relatively low temperature (normal temperature to 500 ° C.) in the temperature rising process up to a predetermined heating temperature,
In addition, a technique for realizing decomposition of organic halide remaining in a heating residue such as residual ash at a low temperature has not been established yet.

[0011]

The present invention has been made to solve the above problems. It is an object of the present invention to provide a soil production method for producing clean soil from soil contaminated with organic halides such as dioxins, and a soil treatment device.

Another object of the present invention is to provide a processing method and a processing apparatus for safely processing an object to be processed such as incineration ash and shredder dust.

Further, according to the present invention, generation of dioxin is prevented as much as possible and the concentration of dioxin remaining in the heating residue is suppressed to a low level by means of changing the pressure and temperature in the heating chamber during the heat treatment of the object to be treated. It is an issue.

Further, the present invention is safe and reliable from heating residues such as residual ash generated from garbage incineration facilities and factories of local governments, residual liquid, dioxin contained in soot, etc., soil and sludge contaminated with these. An object of the present invention is to provide a processing method and a processing device capable of removing dioxin.

Further, according to the present invention, it is possible to suppress the generation of dioxin itself by controlling these in accordance with the temperature, pressure, chlorine and oxygen amount in the furnace at the time of pyrolysis, and at the same time, if dioxin is generated. , Or even if residual dioxin is present, it can be reliably decomposed and removed, and moreover, a thermal decomposition method and apparatus capable of effectively treating dioxin even at atmospheric pressure thermal decomposition at a relatively low temperature. The challenge is to provide.

[0016]

In order to solve such a problem, the present invention has the following constitution.

The method for producing soil according to the present invention comprises a second soil containing the organic halide in a second concentration lower than the first concentration from the first soil containing the organic halide in a first concentration. In a method of producing soil for producing soil, at least a part of the organic halide is thermally decomposed by introducing the first soil into an airtight region and heating the first soil under reduced pressure. Characterize. The object to be treated is heated above the decomposition temperature of the organic halide or above the boiling point.

Examples of the organic halide include dioxin, PCB, coplanar PCB and the like.

Further, a step of reducing the halogen concentration in the gaseous effluent generated by the thermal decomposition of the soil may be further included. This can reduce the possibility of organic halides being produced and regenerated in the gaseous effluent.

The pyrolysis residue of the first soil may be cooled after the airtight region is replaced with a replacement gas that is substantially free of the organic halide and has no organic halide forming ability. This makes it possible to prevent organic halides such as dioxins from being fixed in the residue due to cooling.

Examples of the form of the substitution gas which is substantially free of the organic halide and does not have the ability to form an organic halide include, for example, helium, neon, argon, krypton, xenon, nitrogen and hydrogen. At least one selected gas, a mixed gas thereof, and a gas mainly containing these gas or mixed gas can be used.

The thermal decomposition step may be performed while controlling the oxygen concentration in the hermetic zone. As a result, it is possible to suppress fluctuations in the production amount of the gaseous emission regardless of the non-uniformity of the object to be treated, partial combustion, etc., and to perform the treatment of the gaseous emission more reliably and efficiently. Further, by suppressing the oxygen concentration and the halogen concentration, it is possible to prevent dioxin formation.

The method for producing soil according to the present invention comprises a second soil containing the organic halide in a second concentration lower than the first concentration from the first soil containing the organic halide in a first concentration. In a method for producing soil for producing soil, the first soil is heated so that at least a part of the organic halide is evaporated or decomposed, and a heating residue of the soil is introduced into an airtight region, Is replaced with a replacement gas that is substantially free of the organic halide and does not have the ability to form an organic halide, and then the heating residue of the soil is cooled.

The method for producing soil according to the present invention is characterized in that soil containing an organic halide is pyrolyzed under reduced pressure. Under reduced pressure, the mean free path of molecules is long, and since the system is kept in a non-oxidizing atmosphere, it is possible to prevent the formation and regeneration of organic halides such as dioxins. Moreover, since the partial pressure of the organic halide itself is small under reduced pressure, the concentration of dioxins remaining in the heating residue can be reduced.

[0025] For example, by subjecting soil containing residual dioxins, heating residues, steamed products, residual ash, residual liquid, soot dust, etc., generated from waste treatment facilities and factories to heat treatment while reducing pressure from normal pressure and increasing temperature. Dioxins can be effectively treated.

The halogen concentration of the gaseous effluent generated by the thermal decomposition of the soil may be reduced.

The soil treating apparatus of the present invention is a soil treating apparatus for treating soil containing an organic halide or capable of producing an organic halide by heating, a means for heating the soil, and an airtight region. A means for introducing a heating residue of the soil into an airtight area, a means for substantially replacing the inside of the airtight area with the organic halide-free (being deficient in organic halide) replacement gas, and And means for cooling the residue. In the present invention, regardless of combustion, pyrolysis, reduced pressure pyrolysis,
After heating the soil, which is the object to be treated, it is purged and cooled in the airtight region. The replacement means may introduce the replacement gas after depressurizing the airtight region.

A metal which forms a compound with halogen contained in the gaseous effluent produced by heating the soil,
Alternatively, a halogen removing means may be further provided in which an adsorbent for adsorbing halogen in the gaseous emission is arranged.

Further, the reforming means for reforming the gaseous effluent generated by heating the soil at the first temperature such that dioxin is decomposed, and the increase of the dioxin concentration in the reformed gaseous effluent are Cooling means for cooling the gaseous effluent to a second temperature so as to be suppressed. As the cooling means, oil may be jetted to the gaseous emission for rapid cooling.

That is, the treatment method of the present invention is characterized by thermally decomposing an object to be treated containing an organic halide under reduced pressure.

The processing apparatus of the present invention is a processing apparatus for processing an object to be processed which contains an organic halide or is capable of producing an organic halide by heating, and means for heating the object to be processed and airtightness. An area, means for introducing the heating residue into the airtight area, and means for replacing the inside of the airtight area with the organic halide-free (being deficient in organic halide) replacement gas.
A means for cooling the heating residue is provided. Examples of the heating means include a combustion furnace that burns the object to be treated, a pyrolysis furnace that thermally decomposes the object to be treated, a decompression pyrolysis furnace that thermally decomposes the object to be treated under reduced pressure, and the like.

The treatment apparatus of the present invention is a furnace in which the pyrolysis temperature can be controlled or a plurality of decompression furnaces having different pyrolysis temperatures are used for pyrolyzing (steaming) the object to be treated while decompressing the object from normal pressure. It is characterized by passing through. For example, the pressure in the furnace may be treated substantially constant, and the object to be treated may be thermally decomposed while changing the temperature.

Further, a furnace capable of controlling the pyrolysis temperature for pyrolyzing the object to be treated is provided, and the inside of the furnace is changed from normal pressure to a predetermined degree of vacuum so that the degree of vacuum can be maintained. It is characterized by For example, the temperature in the furnace may be kept substantially constant, and the object to be treated may be thermally decomposed while changing the pressure.

Further, a normal pressure furnace for thermally decomposing the object to be treated and a plurality of decompression furnaces may be connected in series, and the pyrolysis temperature in each of the furnaces may be set so as to increase toward the subsequent stage.

A metal that forms a compound with the halogen contained in the gaseous emission produced by the thermal decomposition of the object to be treated, which is arranged in connection with the decompression furnace, or the halogen in the gaseous emission, is adsorbed. It is characterized in that it further comprises a halogen removing means holding the adsorbent therein.
For example, a portion of the halogen removing means that is loaded with a metal that traps halogen, a catalyst that decomposes, or the like is at room temperature to about 1
In the range of about 000 ° C, more preferably about 400 ° C to about 1
You may make it hold | maintain at substantially constant temperature in the range of 000 degreeC. It is preferable to keep the portion that adsorbs halogen at a low temperature.

Further, in the present invention, the heating residue containing residual dioxins from the waste treatment facility or factory may be treated while being decompressed and heated. Further, steamed foods, residual ash, residual liquid, soot dust, etc. containing residual dioxins generated from waste treatment facilities, factories, etc. may be treated while reducing the pressure from normal pressure and raising the temperature.

Further, according to the present invention, the gaseous effluent is decomposed and reduced by introducing the gaseous effluent into the heated reducing means arranged at the gas outlet of the heat-decomposable furnace, which can be sealed. Oxygen, oxide gas, chlorine,
At least one gas concentration of chloride gas may be measured, and the temperature, pressure, oxygen concentration, etc. in the pyrolysis furnace may be controlled according to the measured value.

In addition, by introducing the gaseous effluent into the reducing means in a heated state disposed at the gas outlet of the heat-decomposable furnace, the gaseous effluent is decomposed and reduced, and the inside of the thermal decomposition furnace or Oxygen on the downstream side of the reducing means, oxide gas,
At least one gas concentration of chlorine and chloride gas may be measured, and a metal reducing agent may be supplied into the thermal decomposition furnace according to the measured value.

Further, in the processing apparatus of the present invention, a retort capable of raising the temperature is provided at the gas outlet of the heat-decomposable pyrolysis furnace, and at least one of oxygen and oxide gas and at least chlorine and chloride gas are provided downstream thereof. One of the gas concentration measuring means may be arranged and the temperature inside the furnace may be controlled based on the value measured by the gas concentration measuring means.

Further, a reduction retort capable of raising the temperature is provided at the gas outlet of the heat-sealable pyrolysis furnace, and a gas concentration measuring means for at least one of oxygen and oxygen gas and at least one of chlorine and chloride gas is provided downstream thereof. A metal reducing agent supply means for supplying a metal reducing agent such as aluminum or magnesium is installed in the furnace based on the value measured by the gas concentration measuring means, so that the amount of oxygen and chlorine in the furnace, the furnace You may make it control internal pressure and temperature.

For example, the gas concentration of at least one of oxygen and oxide gas and at least one of chlorine and chloride gas in the thermal decomposition furnace or downstream of the reducing means is measured, and the thermal decomposition is performed according to the measured value. By supplying a metal reducing agent such as aluminum or magnesium into the furnace, the oxygen concentration and chlorine concentration in the pyrolysis furnace, and the temperature in the furnace,
You may make it control pressure etc.

It should be noted that the thermal decomposition furnace may be provided with a pressure reducing means to perform thermal decomposition under reduced pressure. In that case, it is preferable to use a liquid ring pump such as a water ring pump as an exhaust system when the thermal decomposition of an object to be treated containing water such as household waste and shredder dust under reduced pressure. The sealing liquid of the liquid ring pump is not limited to water, and an organic solvent may be used. Usually, the thermal decomposition device is
It is equipped with a metal recovery device by condensation and a powder removal device. The powder removing device is composed of a metal powder filter and an oil film powder trap that dissolves and captures powder such as dioxins by passing the gaseous emission through an oil film such as a cloth soaked in oil. The present invention further comprises a plurality of the above pyrolysis furnaces,
A separation chamber that allows gas separation and pressure equalization between adjacent pyrolysis furnaces and that can temporarily store objects to be processed is arranged between the pyrolysis furnaces, and a purge chamber and a rear chamber are provided in the front chamber. A continuous thermal decomposition device having a cooling chamber may be provided. Further, a metal reducing agent and / or an alkali metal hydroxide or an alkaline earth metal hydroxide may be added to the reducing means. In addition, the gaseous effluent generated by thermal decomposition undergoes a process of collecting evaporated metal by condensation, a powder removal process by an oil tank with an oil film, a salt production process by contact with an alkaline solution, and a salt removal process by an ion exchange resin film. You may make it process.

In the present invention, the organic halide includes dioxins, PCB, coplanar PCB, DDT, trichlorethylene, trihalomethane and the like (see FIG. 6).

In the present invention, unless otherwise specified, polychlorinated dibenzoparadioxin (Polychlo) is used.
lined dibenzo-p-dioxin
s: PCDDs), polychlorinated dibenzofuran (Pol
ychlorinated dibenzofuran
s: PCDFs) and their homologues having different chlorine numbers and substitution positions are collectively called dioxins. Further, a compound obtained by substituting chlorine of dioxin with other halogen such as fluorine or bromine is also included in the organic halide in the present invention.

In order to reduce the concentration of organic halides such as dioxins, PCBs and coplanar PCBs in the heating residue of the object to be treated, the treatment is carried out at a temperature at which at least a part of such organic halides is decomposed. It is important to heat the object to be treated and to cool the object to be treated in an atmosphere in which the concentration of the organic halide and the substance capable of forming an organic halide is as low as possible.

On the other hand, it is preferable to reduce the concentration of dioxins, for example, the concentration of substances capable of producing dioxins such as halogen as much as possible also in the gaseous emission generated by heating the object to be treated.

If an organic halide coexists in the cooling atmosphere when the object to be treated is cooled, the organic halide is fixed in the object to be treated. In addition, when a material substance capable of forming an organic halide coexists during cooling of the object to be treated, the organic halide is synthesized or re-synthesized during the cooling process, and the organic halide remains in the residue. Will end up.

Therefore, in the present invention, in treating an object to be treated which contains an organic halide or produces an organic halide by heating, combustion,
After heating such as thermal decomposition, the heating residue is cooled in a state where the concentration of the organic halide and the substance having the ability to form an organic halide is reduced. Therefore, the heating residue may be cooled in an atmosphere purged with a cooling gas containing no organic halide material, for example. Therefore, it is preferable to use a gas containing no halogen, oxygen, or organic compound as the cooling gas, and for example, a rare gas such as argon, nitrogen, or the like can be used.

Examples of the object to be treated are municipal waste, incinerated ash of municipal waste, soil contaminated with organic halides such as dioxins and PCBs, sludge, agricultural products, marine products, shredder dust, waste home electric appliances and various wastes. Can be raised.

The treatment method of the present invention is a treatment method for treating an object to be treated capable of producing an organic halide by heating, wherein the object to be treated is heated, and the heating residue is introduced into an airtight region, The inside is replaced with a replacement gas that is substantially free of the organic halide and has no ability to form an organic halide, and the heating residue is cooled.

Further, the treatment method of the present invention is a treatment method of treating an object to be treated capable of producing an organic halide by heating, wherein the object to be treated is heated, and the heating residue is introduced into an airtight region, It is characterized in that the inside of the region is replaced with the organic halide-free (the organic halide is deficient) replacement gas, and the heating residue is cooled. Here, “organic halide-free” means that the organic halide is deficient. The form of the replacement gas is noble gas, nitrogen, hydrogen,
Alternatively, a mixed gas of these can be given. Further, air can be used as the replacement gas as long as the oxygen concentration does not matter.

The heating mode of the object to be treated is as follows:
For example, combustion, thermal decomposition, etc. can be mentioned. Such heating may be performed while adjusting the oxygen concentration. The thermal decomposition may be performed while adjusting the pressure in the airtight region such as depressurization or pressurization.

The introduction of the replacement gas into the airtight region may be performed after depressurizing the airtight region.

The gaseous emission produced by heating the object to be treated is also treated to reduce the concentration of organic halides such as dioxin.

As such a treatment, for example, the gaseous effluent is reformed at a first temperature at which dioxin is decomposed, and an increase in the dioxin concentration in the reformed gaseous effluent is suppressed. So that the gaseous emissions are second
You may make it cool to the temperature of.

Cooling of the gaseous effluent produced by heating the object to be treated may be carried out by injecting oil into the gaseous effluent to quench it. This makes it possible to suppress the re-synthesis of the organic halide and trap the hydrocarbons and the like in the reformed gaseous exhaust.

Further, the gaseous effluent cooled by spraying oil is reheated to a high temperature at which organic halides such as dioxins are decomposed again, and then cooling water is sprayed to quench it. Good. This cooling water may be made alkaline.

Further, the concentration of halogen such as chlorine contained in the gaseous emission produced by heating the object to be treated may be reduced. For example, a halogen removing device or the like for removing halogen in the gaseous emission may be provided at the subsequent stage of the thermal decomposition furnace. Examples of the form of the halogen removing device include a metal such as iron that reacts with chlorine in the gaseous emission in the chamber to form a chloride, a Dalai powder, and / or
Alternatively, there is one loaded with a compound such as calcium hydroxide. Further, the chamber may be loaded with a catalyst that accelerates the fixing reaction of halogen in the gaseous effluent or the decomposition of the organic halide in the gaseous effluent. Further, an adsorbent that adsorbs halogen contained in the gaseous emission may be loaded. A plurality of these halogen removing devices may be combined.

When using an adsorbent such as zeolite for removing halogen, it is preferable to keep the adsorbent at a temperature as low as possible in order to improve the adsorption efficiency.
In this case, the gaseous effluent will be cooled in the chamber loaded with the adsorbent, and this cooling will be carried out when the temperature of the gaseous effluent stays in the regeneration temperature range of organic halides such as dioxins. It is preferable to do so rapidly so that is as short as possible.

The above-mentioned various treatments for reducing the concentration of the organic halide such as dioxin in the gaseous emission may be used in combination.

As the processing apparatus of the present invention for realizing such processing, for example, an airtight area capable of holding an object to be processed airtight, means for adjusting the temperature of the airtight area, and inside the airtight area It is sufficient to include a replacement means for replacing the gas of 1) and a cooling means for cooling the heating residue of the object to be treated. Further, the pressure inside the airtight region may be reduced.

The replacement means may not only replace the gas in the airtight region, but may also reduce the pressure in the airtight region and exhaust it before introducing the replacement gas. This exhaust system can also be used for depressurization in the hermetic zone other than gas replacement.

Further, moving means for moving the object to be processed in the airtight region may be provided. The moving means may include a rotary kiln, a screw conveyor, a tray pusher, a drawer, a roller house, and the like.

A gas circulating device may be provided to circulate the gas inside the airtight region while adjusting the temperature.
As a gas circulation device, for example, a bypass connected to an airtight region (chamber) is provided, and a circulation pump,
Temperature control device or heat exchanger, dust contained in gas stream,
A filter means for removing mist or the like may be provided. These may be arranged in the order of the filter, the temperature control device, and the circulation pump. In particular, it is preferable that the filter is arranged before the circulation pump and the temperature control device. For example, an oil film may be used as the filter.

The above-described treatment method and treatment apparatus of the present invention can be applied not only to a reduced pressure pyrolysis furnace but also to a treatment in a heating furnace such as an incinerator or an atmospheric pressure pyrolysis furnace.

For example, the treatment apparatus of the present invention can be attached after the conventional incinerator and atmospheric pressure pyrolysis furnace. Therefore, organic halides such as dioxins can be safely and effectively removed from a large amount of incineration residues generated in an incinerator.

Diffusion of toxic organic halides into the environment is a serious problem, and it takes enormous cost and time to rebuild the incineration facility with a new treatment facility, and the waste generated daily Processing must also be done. The present invention can also be applied to an existing incineration facility as an incidental facility. Therefore, it is possible to process an object to be processed having an organic halide-forming ability while using the existing equipment.

The method for producing soil according to the present invention comprises a second soil containing the organic halide in a second concentration lower than the first concentration from the first soil containing the organic halide in the first concentration. In the method of producing soil for producing soil, the step of introducing the first soil into an airtight region, and the step of thermally decomposing at least a part of the organic halide by heating the first soil under reduced pressure. And are included.

The pyrolysis residue of the first soil is preferably cooled after the airtight region is replaced with a replacement gas that is substantially free of the organic halide and does not have the ability to form an organic halide.

As described above, if an organic halide coexists in the cooling atmosphere when the object to be treated is cooled, this organic halide is fixed in the heating residue in the object to be treated. Is. In order to remove the organic halide from the heating residue of the object to be treated, in which the organic halide is evaporated by heating or the organic halide is generated, the heating atmosphere gas containing the organic halide is replaced or the pressure is reduced. It is important to cool the heating residue while reducing the concentration of the organic halide and the substance capable of forming the organic halide. Therefore, by cooling the thermal decomposition residue of the first soil in a state in which the concentration of the organic halide or the substance having the ability to form an organic halide is reduced, the second residue that is the heating residue of the first soil can be obtained. The concentration of organic halides remaining in soil can be reduced and removed.

The thermal decomposition of the first soil is preferably carried out while controlling the oxygen concentration in the hermetic zone. For example, the oxygen concentration in the airtight region may be measured, and the oxygen concentration in the airtight region may be adjusted according to the measured oxygen concentration. The control of the oxygen concentration may be performed by introducing a reducing carrier gas or a reducing agent into the airtight region.

By actively controlling the oxygen concentration in the airtight region in this way, even if the object to be treated is heterogeneous, it can be thermally decomposed in a stable state. Further, by performing thermal decomposition while maintaining the airtight region in a reducing atmosphere, it is possible to suppress the production of organic halides such as dioxins. Furthermore, by reducing the pressure in the airtight region, the mean free path between molecules becomes longer, and the probability of formation of organic halides such as dioxins can be reduced.

When the first soil contains a metal such as a heavy metal, the soil may be heated and decompressed to vaporize and recover the metal. By doing so, even if the soil is contaminated with mercury, cadmium, zinc, lead, arsenic, etc., such metal can be separated and recovered from the soil. Also
Hexavalent chromium can be reduced to, for example, trivalent chromium.

The present invention is not limited to contaminated soil but can be similarly applied to the treatment of incinerated ash, sludge, waste liquid, agricultural products, marine products and the like. Since the soil treated according to the present invention contains a large amount of inorganic components such as porous carbon, it can be used not only as soil but also as an effective soil improver. Further, it may be used by mixing with organic matter such as mulch and compost.

Further, the treatment method of the present invention is characterized in that, when cooling the heating residue of the object to be treated capable of producing dioxin by heating, the dioxin concentration in the atmosphere is reduced to cool the heating residue. .

Further, not only the concentration of dioxin itself in the cooling atmosphere, but also the concentration of substances that are raw materials of dioxins (for example, concentration of chlorine, oxygen, organic matter, etc.),
Alternatively, it is preferable to reduce the concentration and amount of the catalytic substance that promotes the dioxin formation reaction.

In the processing apparatus of the present invention, an airtight region inside which an object to be processed can be kept airtight, a means for adjusting the temperature of the airtight region, and a replacement for replacing the gas in the airtight region. Means and cooling means for cooling the heating residue of the object to be treated may be provided. The replacement means may not only replace the gas in the airtight region, but may decompress and exhaust the air in the airtight region and then introduce the replacement gas. This exhaust system can also be used for depressurization in the hermetic zone other than gas replacement. Further, a moving means for moving the object to be processed in the airtight region may be provided. The moving means may include a rotary kiln, a screw conveyor, a tray pusher, a drawer, a roller house, and the like.

A gas circulating device may be provided for circulating the gas inside the airtight region while controlling the temperature.
As a gas circulation device, for example, a bypass connected to an airtight region (chamber) is provided, and a circulation pump,
Temperature control device or heat exchanger, dust contained in gas stream,
A filter means for removing mist or the like may be provided. These may be arranged in the order of the filter, the temperature control device, and the circulation pump. In particular, it is preferable that the filter is arranged before the circulation pump and the temperature control device. For example, an oil film may be used as the filter.

Further, in the processing apparatus of the present invention, a decomposition reaction removing apparatus, which is connected to the airtight region and decomposes, reacts, and removes a gaseous emission generated from the object to be processed, and a decomposition reaction removing apparatus which is consequent thereto. An alkaline water (oil) gas ejector type (venturi) cooling device for quenching gas and reacting with alkali, and a circulation device connected to it for making the cooling medium (water, oil) used in the cooling device alkaline You may The circulation device may be equipped with a filter for removing dust in the alkaline water.

Further, in the processing apparatus of the present invention, a removing device connected to the cooling device described above for removing water from the gas containing water, which is discharged from the cooling device, and a toxic component in the gas after the removal of the water due to the removal device are adsorbed. An adsorbing device and a suction device for sucking (exhausting) gas emitted from the adsorbing device may be provided.

Further, the processing apparatus of the present invention comprises a gas decomposition apparatus for heating and decomposing gas generated from an object to be processed, a vacuum door connected to the gas decomposition apparatus for shutting down the furnace, a condensing apparatus connected to the vacuum door for collecting evaporate, and connected to the vacuum apparatus. Dust removal device for removing dust, vacuum valve connected to it to shut off and collect condensate from the furnace body during operation, and pressure control to connect to it and adjust the pressure in the airtight region (decompression, pressurization) Means and means are provided.

Further, a gas decomposing device for heating and decomposing gas exhausted from decompression means such as an exhaust system provided in the pressure adjusting device, and an alkaline water (oil) gas ejector type for quenching the decomposed gas to react with alkali A (Venturi) cooling device, an adsorbing device that adsorbs a toxic component in the gas after removing the water, and a suction device that sucks (exhausts) the gas emitted from the adsorbing device may be provided.

Further, in the continuous processing apparatus of the present invention, at least two airtight chambers partitioned by the airtight region and a vacuum door are further provided on the inlet side of the airtight region, and at least one of the two airtight chambers is provided. A pressure reducing device for reducing the pressure is provided.
The two airtight chambers are also separated by a vacuum door. The airtight chamber is equipped with a tray (jig) for storing the object to be processed.

Then, a moving device for moving the tray between the two hermetic chambers, a charging device for charging the object to be treated contained in the tray from the hermetic chamber adjacent to the hermetic region to the hermetic region, and the hermetic chamber. A transport means for transporting the object to be treated placed in the area to the outlet side of the airtight area while heating the object. The object to be treated is cooled from the airtight area,
It is discharged on the page by air etc.

At the outlet of the object to be treated in the airtight container, there is a storage chamber capable of airtightly storing the heating residue,
A cooling chamber for cooling the heated residue, a purge chamber for replacing the atmosphere with a replacement gas or an exhaust system to store an empty tray, and a discharge chamber for discharging the heated residue to a conveyor or the like at normal pressure are provided. Each of these four chambers may be equipped with a vacuum door so that it can be kept airtight independently. Further, since the charging chamber may be at normal pressure, the three chambers may be made airtight. Then, the heating residue is conveyed by moving a jig such as a tray through these four chambers. In order to facilitate movement, these chambers may be provided in a grid shape (for example, each chamber is provided at each vertex of a quadrangle). For transporting the heating residue from the airtight container to be subjected to the heat treatment to the storage chamber, the storage chamber may be provided below the airtight container in addition to various transporting means, and the heating residue may be dropped by gravity.

[0086]

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS (Embodiment 1) An embodiment of the present invention will be described with reference to the accompanying drawings. FIG. 1 is a diagram showing an overall configuration of a thermal decomposition apparatus according to the present invention for carrying out a method according to the present invention, and FIG. 2 is a diagram showing a main part thereof.

The thermal decomposition furnace 1 is provided with a control device 2 for controlling the temperature inside the furnace, a recovery device 3 for evaporated metal, a reducing means in the furnace, a heating means 20 and a cooling means 21 in the furnace. In addition, by installing a structure and mechanism for decompressing, which will be described later with the vacuum valves 40, 42 and subsequent parts,
It is also possible to enable recovery of valuables as a vacuum pyrolysis furnace. In addition, the pyrolysis furnace 1 has a temperature sensor, a vacuum sensor,
A sensor group 5 consisting of oxygen and oxide concentration sensors, chlorine and chloride concentration sensors, etc. is arranged, whereby
The temperature in the furnace, the degree of vacuum, the concentration of at least one of oxygen and oxide gas, etc. are measured, and the data signal is sent to the control device 2. The thermal decomposition furnace 1 is surrounded by a heat insulating material, and a vacuum door 17 which is driven up and down by an air cylinder or the like is provided at a carry-in entrance of the object 18 to be treated. The object 18 to be processed is loaded into the furnace by opening the vacuum door 17 while being housed in the jig 19. In the thermal decomposition furnace 1, a stirring means 23 for the object to be treated 18 is installed outside the heating means 20 and the cooling means 21 in the furnace, if necessary. The stirring means 23 shown in the figure is a fan, but it is not limited to this, and instead of or in addition to it, the stirring target 23 enters the jig 19 to be treated 18
You may arrange the screw which stirs, and you may employ the rotary kiln system which rotates with the furnace. Usually,
A heater is used as the heating means 20, and a nitrogen gas circulation circuit is used as the cooling means 21. The nitrogen gas circulation circuit 21 includes a water-cooled cooler for cooling the nitrogen gas.
24 and a pump 25 for circulating nitrogen gas in the thermal decomposition furnace 1 are installed. It is more preferable that the circulation circuit further includes a filter.

A reducing retort 4 as an in-furnace reducing means is arranged in the gaseous emission reducing portion which is brought into contact with the thermal decomposition furnace 1. The reducing retort 4 is filled with a metal reducing agent such as aluminum powder alone or with an alkali hydroxide, and a temperature sensor 5a for detecting the temperature in the reducing retort 4 is provided. In the heat insulation material surrounding the reduction retort 4, the inside of the reduction retort 4 is about 800 ° C to about 1200 ° C.
A heater 7 capable of heating up to about ℃ is embedded.
Reduction gas outlet 8 formed on the downstream side of the reduction retort 4
Inside, an oxygen concentration sensor 5b and a chlorine concentration sensor 5c are provided. The reducing gas outlet 8 communicates with the subsequent recovery device 3, and a vacuum door 26 having vacuum resistance, which is normally driven up and down by a cylinder, is installed in the middle thereof. Evaporants generated in the thermal decomposition furnace 1 are introduced into the recovery device 3, and the gaseous effluent serves to remove dioxin generated by heating and residual dioxin in the object to be treated 18. As is well known, dioxins are generated in a temperature range of 200 ° C or higher, and dioxins and the like in residual ash decompose at temperatures of 500 ° C or higher. Pyrolysis in Pyrolysis Furnace 1 is atmospheric pressure pyrolysis in the range of around 500 ° C, and a large amount of dioxin is generated.
By introducing into the reduction retort 4 heated above ℃, dioxin in the gas is decomposed and oxygen and chlorine atoms are dissociated. The dissociated oxygen and chlorine are immediately removed by causing a chemical reaction with a metal reducing agent having a small reaction energy such as aluminum and magnesium filled in the reduction retort 4, and again contribute to the generation of dioxin. Even if the reduction retort 4 is used, oxygen and chlorine are not completely removed. Especially, when the decomposition by the thermal decomposition is too early, the removal of them becomes incomplete, and they flow out to the reducing gas outlet 8. Therefore, the oxygen concentration sensor 5b and the chlorine concentration sensor 5c detect and analyze the concentrations of at least one of the outflowing oxygen and oxide gas, and at least one of chlorine and chloride. Take measures such as lowering the temperature or stopping heating to delay decomposition. Also,
When equipped with a decompression means, the decompression process reduces the generation of oxygen and chlorine and prevents the formation of dioxins. Since it is not possible to analyze the mixed component ratio of the gas, the concentration analysis of oxygen and oxide by the oxygen concentration sensor 5b may be performed for at least one of O ₂ , CO, CO _2, etc. The concentration analysis of chlorine and chloride by the sensor 5c may be performed for any one of Cl ₂ , HCl, HClO and the like. Immediately after the object 18 to be treated is put into the pyrolysis furnace 1, the cooling means 21
To purge the inside of the furnace with nitrogen gas, or, if a decompression means is provided, evacuate the inside of the furnace to about 1 to 10 ^-2 Torr to heat it after reducing the amount of oxygen in the system. It is possible to reduce the consumption of the reducing agent. Further, in the thermal decomposition apparatus of the present invention, the oxygen concentration sensor 5b and the chlorine concentration sensor 5c in the above embodiment are arranged not in the reducing gas outlet 8 but in the thermal decomposition furnace 1 and the thermal decomposition furnace 1 is provided with aluminum in the furnace. Reducing agent supply means 22 for supplying a powdery, liquid or gaseous metal reducing agent such as magnesium, zinc, etc.
Is installed, and other configurations are the same as those in the first embodiment.

In this case, the oxygen concentration sensor 5b and the chlorine concentration sensor 5c respectively detect and analyze the concentrations of oxygen, chlorine and the like in the thermal decomposition furnace 1, and when the concentration exceeds a predetermined value, the furnace is detected according to the detected value. While the temperature rise of the internal temperature is stopped, a metal reducing agent such as aluminum or magnesium is supplied from the reducing agent supply means 22 into the thermal decomposition furnace 1. As a result, aluminum oxide, aluminum chloride, etc. are generated, and therefore the amounts of oxygen and chlorine in the thermal decomposition furnace 1 and the pressure are controlled, and the generation of dioxins is prevented.

Next, with reference to FIG. 1, a description will be given of the configurations of the evaporated metal recovery device 3, the powder removing means, the vacuuming means, etc. which may be commonly installed in the present invention. The recovery device 3 is surrounded by a water-cooled space 27 and has a vacuum door 28 on one side, from which a recovery retort 29,
Even during the evaporation work, the vacuum door 2 by the cylinder (not shown)
It can be pushed to the reducing gas outlet 8 via 6. Further, by opening and closing the vacuum door 26, the recovery retort 29 can be taken in and out during the evaporation work. The recovery device 3 is provided with a recovery product cooling means 30 by nitrogen gas circulation similar to that in the thermal decomposition furnace 1 so that the recovery product can be cooled quickly.

A powder filter is connected to the subsequent stage of the recovery device 3 to capture the powder which has not been recovered by the recovery device 3. The powder filter is a wire mesh powder filter 31.
And an oil powder trap 32.

As shown in FIG. 3, the oil powder trap 32 has a bottom portion in which an oil 34 is stored in a casing 33 which stores the oil 34 in the bottom.
An oil film 35 usually made of cloth dipped in is stretched, and the gas that has passed through the wire mesh powder filter 31 is forcibly guided to the oil film 35 and allowed to pass therethrough, whereby the powder is captured by the oil film 35. The oil 34 rises in the oil film 35 by a capillary phenomenon to form an oil film, captures the powder in the gas passing therethrough, and falls into the oil 34 together with the powder.

In particular, the oil powder trap 32 is effective for capturing and removing dioxin, which has a property of being easily dissolved in oil. The oil powder trap 32 includes a pump 36, a filter 37, and an oil / water separator 38.
9 is installed, in which oil-water separation and trapped powder removal in the oil 34 are performed.

Next, the structure of the vacuum system connected to the recovery system will be described. In this example, the evacuation system is divided into a main system that operates when the inside of the pyrolysis furnace 1 has a predetermined vacuum degree (for example, 10 ⁻³ Torr) or less, and a sub system that operates when the inside of the pyrolysis furnace 1 becomes higher than that. There is. The main system includes a booster pump 41 and a water seal pump 47 that are installed via the vacuum valve 40, and the sub system includes a diffusion pump 43 and a rotary pump 44 that are installed via the vacuum valve 42.

An oil rotary pump is generally used as a vacuum pump for evacuating the inside of the system, but this exhaust means may be unusable when water is mixed. Therefore, in the present invention, the water ring pump 47 is used as the exhaust system in consideration of performing the thermal decomposition treatment of the object to be treated, such as household waste and shredder dust, which generates a large amount of water.
May be used.

The booster pump 41 and the water seal pump 47 operate to raise the degree of vacuum in the pyrolysis furnace 1 to discharge the gaseous emission in the furnace, but the thermal decomposition proceeds and the gaseous emission in the furnace progresses. When the amount of material decreases and reaches a predetermined degree of vacuum, the vacuum valves 40 and 42 and other valves open and close, and the gas flow moves from the main system to the sub system. This sub-system is mainly used for metal recovery, element removal and the like. The sub-system diffusion pump 43 and rotary pump 44 operate to maintain the inside of the thermal decomposition furnace 1 at a vacuum degree higher than or equal to the predetermined vacuum degree, and recover the evaporated material. In addition, 45
Is a holding pump that assists the diffusion pump 43 together with the rotary pump 44.

On the downstream side of the booster pump 41, a chlorine, NOx, SOx, etc. removing device utilizing the water circulation of the water ring pump 47 is installed. Chlorine removal device is a water ring pump 4
In addition to 7, a water seal pump water tank 48, a filter 49, an oil / water separator 50, an alkaline water supply tank 51, an ion exchange resin layer 52, a cooler 53, and a pump 54 are included.

The alkaline water tank 51 is connected to an alkaline tank 55 which is usually a solution tank of calcium hydroxide or sodium hydroxide, and the water in the alkaline water tank 51 is pumped by the pump 5.
The water is circulated in the alkaline tank 55 by 6 and the pH-adjusted water is sent to the ion exchange resin layer 52.

The ion-exchanged water from which salts such as sodium chloride have been removed by passing through the ion-exchange resin tank 52 is cooled by the cooling water 53 and then sent into the water-sealed vacuum pump 47 by the action of the pump 54. . Water-sealed vacuum pump 47
Gas is sent from the main system of the vacuum system,
The chlorine gas, NOx, SOx, etc. contained in this gas are converted into salts such as calcium salt or sodium salt by causing a chemical reaction with the alkaline solution in the water-sealed vacuum pump 47, and the water-sealed pump water tank. Sent to 48.
A part of this salt is a part of the exchange resin tank 5 as described above.
Removed in 2.

Gas and aqueous solution are sent from the water-sealed vacuum pump 47 to the water-sealed pump water tank 48. Since mercury precipitates and accumulates at the bottom there, it is taken out by opening the cock at an appropriate time. The water-sealing pump water tank 48 is equipped with an adsorption device 58 and a pump 59 as an exhaust system, and the degassing path 5 is provided.
7 is installed so that the gas sucked by the action of the pump 59 is introduced into the adsorption device 58. The adsorption device 58 includes activated carbon, an adsorbent such as zeolite, and a catalyst such as vanadium oxide that decomposes dioxin and the like, and mainly adsorbs and removes harmful components in the gas. The gas from which the harmful components have been removed in this way is discharged by the action of the pump 59.

In the apparatus according to the present invention having such a configuration, the oxygen concentration sensor 5b and the chlorine concentration sensor 5 in the sensor group 5 during the thermal decomposition under reduced pressure as described above.
The concentration of oxygen and chlorine in the thermal decomposition furnace 1 is detected by c, and aluminum and aluminum oxide are generated in the thermal decomposition furnace 1 from the reducing agent supply means 22 in accordance with the detected values. And the amount of oxygen and the degree of vacuum are controlled.

Further, the gaseous effluent generated in the low temperature region is introduced into the reduction retort 4 and decomposed by heat, and chlorine, oxygen and the like are contained therein as a metal reducing agent or a hydroxide of an alkali metal or an alkaline earth metal. Are captured and removed by.

In the present invention, not only the oxygen concentration but also
It is also preferable to measure the concentration of an oxide gas such as carbon monoxide or carbon dioxide. This is because the gaseous emission is a mixed gas of various decomposition products, and oxygen analysis may not be performed accurately in the ppm order. Aluminum powder is suitable as the reducing agent. This is because aluminum powder is inexpensive, has the second smallest reaction energy after magnesium, and undergoes a redox reaction such as 2O ₂ + 3Al → Al ₃ O ₄ even at low temperatures.

The gaseous emission generated in the thermal decomposition furnace 62 is introduced into the recovery device 3 by opening the vacuum door 26 as described above, and in the recovery retort 29, cadmium, lead, zinc, chromium, nickel, etc. Of metal vapor,
Water, oil, etc. are condensed and collected.

In the thermal decomposition furnace 1, the heating means 20 and the cooling means 21 are installed in one chamber as described above, but a purge chamber 61 for introducing the object 18 to be treated and performing preliminary vacuuming,
A three-chamber structure having a heating chamber 62 provided with a reducing means for performing vacuum heat treatment and a cooling chamber 63 for cooling the processed product can be adopted. (See Figure 4). In this case, a vacuum heat insulation door system and a vacuum evacuation system are connected between the chambers.

When the thermal decomposition furnace 62 has such a three-chamber structure, the processing amount increases, the processing efficiency improves, and unmanned operation is possible.

A plurality of the pyrolysis furnace 62, the recovery system and the vacuuming system may be connected in series. In that case, the processing temperatures in the plurality of pyrolysis furnaces 62 are made different. When they are connected in series, they may be linear, but it is advantageous to arrange them in a square shape or the like in order to save space. FIG. 5 shows, as an example, an apparatus which is provided with four pyrolysis furnaces 62 and has a quadrangular shape as a whole. It includes a purge chamber 71 for introducing the object to be treated, a preheating chamber 72 adjacent to the purge chamber 71, three vacuum heating chambers (corresponding to the pyrolysis furnace 1) 73 to 75, which form the three sides of the quadrangular apparatus, and vacuums. Between the heating chambers, in other words, four separation chambers 76 to 79 arranged at the four corners of the apparatus, and one or a plurality of cooling chambers 80 and 81 adjacent to the final separation chamber 79 are provided.

The object to be processed is transported by the transport roller 82 before the entrance / exit of the purge chamber 71, and after the vacuum door 71a is opened, it is pushed into the purge chamber 71 by the pushing cylinder 83 attached to the transport roller 82. The object to be treated is returned to the purge chamber 71 after the completion of all treatments. That is, the purge chamber 71 doubles as an inlet and an outlet of this device. The purge chamber 71 is provided with an extrusion cylinder 84 for pushing out the object to be treated.
The processed product returned to 1 is extruded out of the room, placed on the transport roller 82, and unloaded. In the figure, a vacuum pump is installed in the purge chamber 71 to perform air replacement.

Cooling chambers 80, 8 with the purge chamber 71 in between.
A transfer conveyor 86 extending from 1 to the preheating chamber 71 and the first separation chamber 76 is arranged. Vacuum doors 87 and 88 are provided on both side surfaces of the purge chamber 71 so that the object to be processed can be moved between the chambers. Bypasses 89 to 99 each having an opening / closing valve (the bypass 96 is installed if necessary) are installed between all the above-mentioned chambers, and each room is opened before opening a vacuum door existing between the chambers. The dynamic pressure between them is achieved.

The preheating chamber 72 is a chamber provided with a heating means for preheating the object to be treated sent from the purging chamber 71 by the transfer conveyor 86 to a maximum of about 150 ° C. in general. Similar to the case, the recovery device 3, the powder filter 31, the booster pump 41, the recovery system below the water-sealed vacuum pump 47, the vacuum system, and the exhaust system are installed via the vacuum door 26. Since the configuration and operation of these gaseous emission treatment systems and the like are the same as those described above, the description thereof will be omitted. In the vacuum heating chamber at 500 ° C. or lower, the reduction retort 4 is provided at the gas outlet in the same manner as above.

Between the preheating chamber 72 and the first separation chamber 76,
A vacuum double door including a heat insulating door 100 facing the preheating chamber 72 side and a vacuum door 101 facing the first separation chamber 76 side is arranged. In addition, the vacuum door 1 facing the first separation chamber 76 side is provided between the first separation chamber 76 and the first vacuum heating chamber 73 adjacent thereto.
02 and a heat insulating door 103 facing the first vacuum heating chamber 73 side, a vacuum double door is arranged. The first separation chamber 76 includes a pushing cylinder 104 that transfers the object to be processed sent from the preheating chamber 72 to the first vacuum heating chamber 73.

The first separation chamber 76 separates the preheating chamber 72 and the first vacuum heating chamber 73 from each other and prevents the vaporized substances from the preheating chamber 72 from flowing into the first vacuum heating chamber 73.
It plays the role of adjusting the degree of vacuum between rooms. In addition, the evaporation material is precipitated there, so that the vacuum sealing property of the vacuum double door is protected. Each of the later-described separation chambers 77 to 79 also performs the same operation as the first separation chamber 76. In addition, each separation chamber 76-7
The vacuum evacuation of 9 is performed by the booster pump 41 in the front chamber (the preheating chamber 72 in the case of the first separation chamber 76) and the water-sealed vacuum pump 4.
Can be done at 7.

The first vacuum heating chamber 73 also has a recovery system and a vacuuming system configuration similar to those of the preheating chamber 72. A first vacuum heating chamber 7 is provided between the first vacuum heating chamber 73 and the second separation chamber 77.
A vacuum double door including a heat insulating door 105 facing the third side and a vacuum door 106 facing the second separation chamber 77 side is arranged. The transfer of the object to be processed into the first vacuum heating chamber 73 and from there to the second separation chamber 77 is carried out by pusher driving by the pushing cylinder 104, tray pusher, etc. (a plurality of objects to be processed are pushed and proceed. ), And the movement after entering the second separation chamber 77 is driven by a roller.

The first vacuum heating chamber 73 has, for example, a vacuum degree of 6
00-10 to ² Torr, temperature is operated at 150-500 ° C, where thermal decomposition of most substances is completed.
The generated gaseous effluent is treated in the reducing agent or reduction retort 4 in the furnace to remove oxygen and chlorine, and further,
The amount of oxygen and chlorine generated is controlled by controlling the temperature and vacuum. This also applies to the following vacuum heating chambers. The second separation chamber 77 receives the object to be processed sent from the first vacuum heating chamber 73 from the second vacuum heating chamber 7.
4 is equipped with a pushing cylinder 107 for feeding. Between the second separation chamber 77 and the second vacuum heating chamber 74, there is a vacuum double door including a vacuum door 108 facing the second separation chamber 77 side and a heat insulating door 109 facing the second vacuum heating chamber 74 side. Will be placed.

The second vacuum heating chamber 74 also has the same configuration of the recovery system, the evacuation system and the exhaust gas system as described above. The second vacuum heating chamber 74 has, for example, a vacuum degree of about 10 ⁻¹ to 10 ⁻³ To.
It is operated at rr and temperature of 500 to 900 ° C., and the purpose is to completely decompose and evaporate the undecomposed components in the thermal decomposition residue and to recover the evaporated metal.

Between the second vacuum heating chamber 74 and the third separation chamber 78, a heat insulating door 110 facing the second vacuum heating chamber 74 side,
A vacuum double door including a vacuum door 111 facing the third separation chamber 78 side is arranged. The transfer of the processed product into and out of the second vacuum heating chamber 74 and the third separation chamber 78 is performed by the pushing cylinder 10.
By the pusher drive by 7, the third separation chamber 78
The movement after entering the inside is by roller drive.

The third separation chamber 78 is provided with a pushing cylinder 112 for feeding the object to be treated sent from the second vacuum heating chamber 74 into the third vacuum heating chamber 75. The third separation chamber 7 is provided between the third separation chamber 78 and the third vacuum heating chamber 75.
A vacuum double door including a vacuum door 113 facing the 8 side and a heat insulating door 114 facing the third vacuum heating chamber 75 side is arranged.

The third vacuum heating chamber 75 is provided with a mechanism in which a diffusion pump 115 and a rotary pump 116 are added to the vacuum evacuation system in addition to the recovery system and the evacuation system similar to the above vacuum heating chamber. Further, the third vacuum heating chamber 75 and the fourth separation chamber 7
A heat insulating door 117 facing the fourth separation chamber 79 side is arranged between the heat insulating door 117 and the second heat insulating door 9. The pusher 112 transfers the object to be processed into the third vacuum heating chamber 75 and from the third vacuum heating chamber 75 to the fourth separation chamber 79.
Is driven by a pusher, and the movement in the fourth separation chamber 79 is driven by a roller.

The fourth separation chamber 79 also serves as the first vacuum cooling chamber, is equipped with a cooling means for the object to be treated, and is provided with a second object to be treated sent from the third vacuum heating chamber 75.
A pushing cylinder 118 for feeding into the cooling chamber 80 is provided. Fourth separation chamber 79 and second cooling chamber 80 adjacent thereto
A vacuum door 119 is disposed between and.

In the second cooling chamber 80, the recovery device 3, the powder filter 31, the booster pump 4 via the vacuum door 26.
1 and the rotary pump 116 are installed, and further, a bypass passage 120 connecting the downstream side of the vacuum door 26 and the purge chamber 71.
Is formed. Further, the second cooling chamber 80 has a vacuum door 121.
The third cooling chamber 81 is connected to the purge chamber 71 through the vacuum door 88.

In such a structure, the object to be treated, which has been conveyed by the conveying roller 82 to the front of the vacuum door 71a of the purge chamber 71, is forced into the purge chamber by bringing air into the same pressure as the outside, and then the vacuum door 71a is opened before being pushed. It is fed into the purge chamber 71 by the cylinder 83, and then the vacuum door 71a is closed. At that time, the vacuum doors 87 and 88 are closed.

In this state, the vacuum pump installed in the bypass 120 operates to reduce the pressure in the purge chamber 71.
Then, by opening the bypass 89, the purge chamber 71 and the preheating chamber 72 are made to have the same pressure, and then the vacuum door 87 is opened. Then, after the object to be processed is sent to the preheating chamber 72 by the conveyor 86, the vacuum door 87 is closed and the bypass 89 is closed.

The preheating chamber 72 has a vacuum degree of 760 to 1 for example.
Torr, the temperature is 0 to 150 ° C., and the decomposition gas generated here through the reduction retort 4 is the vacuum door 26.
When opened, it is guided to the recovery device 3 where the evaporate is recovered, the powder is removed, and the oxygen and chlorine are removed.

After the processing in the preheating chamber 72 is completed, the bypass 90 is opened and the preheating chamber 72 and the first separation chamber 76 are made to have the same pressure. Then, the double vacuum doors 100 and 101 are opened, and the object to be processed is transferred to the first separation chamber 76 by the transfer conveyor 86.
After being transported inside, the double vacuum doors 100, 101 are closed,
Bypass 90 is closed.

Next, after vacuuming the inside of the first separation chamber 76 with the vacuum pumps 41 and 47, the bypass 91 is opened and the first separation chamber 76 and the first vacuum heating chamber 73 are brought to the same pressure. After that, the double vacuum doors 102 and 103 are opened, and the object to be processed is carried into the first vacuum heating chamber 73 by the pushing cylinder 104. In the first vacuum heating chamber 73, for example, in a range of 150 to 500 ° C. under vacuum (vacuum degree of 600 to 10).
-2 Torr) is heated. In this temperature range, most of the organic substances are decomposed and evaporated, and are recovered in the recovery device 3 through the reduction retort 4 and the vacuum door 26 opened. In addition, the removal of powder and the removal of oxygen and chlorine are performed in the same manner as above.

The same applies to the subsequent vacuum heating chambers 74 and 75. That is, after the bypass 92 is opened and the first vacuum heating chamber 73 and the second separation chamber 77 are made to have the same pressure, the double vacuum doors 105 and 106 are opened, and the object to be processed is secondly separated by the pushing cylinder 104. It is carried into the chamber 77. Then, after the double vacuum doors 105 and 106 are closed and the bypass 92 is closed, the bypass 93 is opened and the second separation chamber 77 and the second vacuum heating chamber 74 are made to have the same pressure. Next, the double vacuum doors 108 and 109 are opened, the object to be processed is carried into the second vacuum heating chamber 74 by the pushing cylinder 107, and then the double vacuum doors 108 and 109 are closed and the bypass 93 is closed. When the pressure difference between each separation chamber and the vacuum heating chamber is large, the bypass is opened after adjusting the pressure with the vacuum pump. The same applies to the subsequent vacuum heating chambers 74 and 75.

In the second vacuum heating chamber 74, for example, under a vacuum in the range of 500 ° C. to 900 ° C. (degree of vacuum 10 -1 to 1
Heating at 0-3 Torr). In this temperature range, cadmium, zinc, lead, etc. are decomposed and evaporated, and are recovered in the recovery device 3 through the opened vacuum door 26. Also,
Powder removal and chlorine removal are performed in the same manner as above.

Similarly, the bypass 94 is opened and the second
After the vacuum heating chamber 74 and the third separation chamber 78 are made to have the same pressure,
Double vacuum doors 110 and 111 open, pushing cylinder 10
The object to be processed is transported into the third separation chamber 78 by 7. Then, after the double vacuum doors 110 and 111 are closed and the bypass 94 is closed, the bypass 95 is opened and the third separation chamber 78 and the third vacuum heating chamber 75 are made to have the same pressure. Next, the double vacuum doors 113 and 114 are opened, and the object to be processed is transferred to the third vacuum heating chamber 75 by the pushing cylinder 112, and then the double vacuum doors 113 and 114 are closed and the bypass 95 is closed.

In the third vacuum heating chamber 75, for example, under vacuum in the range of 900 ° C. to 1300 ° C. (vacuum degree of about 10 ⁻²
The heating is performed at about 10 ⁻⁵ Torr). In this temperature range, copper, tin, chromium, etc. are decomposed and evaporated, and are recovered in the recovery device 3 through the opened vacuum door 26. In addition, the powder removal and chlorine removal are performed in the same manner as above.

The third vacuum heating chamber 75 and the fourth separation chamber 79 are always under the same pressure, and after the heat insulating door 117 is opened, the object to be treated is carried into the fourth separation chamber 79 by the pushing cylinder 112. There, the object to be treated is temporarily cooled by a vacuum.

The object to be treated after the completion of the temporary cooling is conveyed to the second cooling chamber 80, but prior to that, the second cooling chamber 80 is carried out.
Then, with the bypass 120 closed, the residual nitrogen gas in the room is discharged by the action of the rotary pump 116 and the booster pump 41. After this processing is performed, the bypass 97 is opened to open the fourth separation chamber 79 and the second cooling chamber 80.
And are made the same pressure. Then, the vacuum door 119 is opened, and the object to be processed is moved to the second cooling chamber 8 by the pushing cylinder 118.
After being transported to 0, the vacuum door 119 is closed and the bypass 97 is closed.

In the second cooling chamber 80, the object to be treated is secondarily cooled with nitrogen gas after the exhausted nitrogen component is replenished. Bypass 9 after completion of this secondary cooling
8, the second cooling chamber 80 and the third cooling chamber 81 are pressure-equalized, then the vacuum door 121 is opened and the object to be processed is transferred to the third cooling chamber 81 by the transfer conveyor 86. Then, the vacuum door 121 is closed, the bypass 98 is closed, and nitrogen cooling is performed in the cooling chamber 81.

When the tertiary cooling by the nitrogen gas in the third cooling chamber 81 is completed, the bypass 99 is opened and the third cooling chamber 81 and the purge chamber 71 are made to have the same pressure, and then the vacuum door 88 is opened. The processed product is carried out to the purge chamber 71 by the transfer conveyor 86. Then, after the vacuum door 88 is closed and the bypass 99 is closed, the pressure in the purge chamber 71 is restored, the vacuum door 71 a is opened, and the processed product is carried out by the extrusion cylinder 84 onto the transport roller 82.

In the third cooling chamber 81, only the nitrogen gas for cooling is exchanged, and the vacuum is not drawn.
Therefore, the processing time is shortened, the installation cost of the vacuum system equipment and the nitrogen gas can be reduced, and the processing amount is increased. (Embodiment 2) A processing device for substituting a gas containing an organic halide such as dioxin at atmospheric pressure (760 Torr) will be described (see FIG. 7).

This processing apparatus comprises a heating device for heating the object to be treated put in a closed container, a cooling device for cooling the heating residue of the object to be treated which is contaminated with the heating device, and a concentration of chlorine, oxygen or the like in the closed container. Is detected and the concentration is controlled based on the detected concentration, a means for transporting the object to be treated, and a replacement means for replacing the gas in the closed container with gas.

In this case, dioxin,
A method for reducing the concentration of organic halides in the heating residue of the object to be treated, which can generate organic halides such as halogenated hydrocarbons, will be mainly explained. Regarding the organic halides generated by heating the object to be treated Also, measures such as recovery and decomposition of the organic halide may be taken.

The residue of the heat treatment such as burning and thermal decomposition of the object to be treated is treated immediately after the heat treatment is completed by purging the heating atmosphere gas containing the organic halide and the substance having the ability to form an organic halide with the replacement gas. The concentration of the organic halide and the substance having the ability to form an organic halide in the container is reduced. Then, the object to be processed is cooled in this state.
This makes it possible to reduce and remove the residual concentration of organic halides such as dioxins in the object to be treated.

As the replacement gas, nitrogen, rare gas such as argon, air, or the like can be used. The requirement for the replacement gas is that it be substantially free of organic halides. Further, it is preferable to use a replacement gas that cannot react with the object to be treated to generate an organic halide. Since air contains oxygen, when it is used as a replacement gas, organic halides may be regenerated during cooling depending on the composition and state of the heating residue. Therefore, it is more preferable to use nitrogen or a rare gas. Further, instead of mere purging, the inside of the container may be depressurized, then purged with a replacement gas (replacement under reduced pressure), and then cooled.

The means for transporting the object to be processed in the container may be selected according to the form of the object to be processed and the processing conditions. For example, screw conveyor, rotary kiln,
A roller house, tray pusher, continuous mesh belt or the like can be used. (Embodiment 3) Next, the decompression replacement process will be described (see FIGS. 8, 9, and 10).

In the apparatus used for this decompression / substitution process, a decompression device for decompressing the inside of the airtight container and a control device for controlling the pressure are further provided in the airtight container of the device described in the above-mentioned replacement at normal pressure. Prepare After the heat treatment of the object to be treated, the inside of the airtight container is vacuum pumped to 10 to 10 ⁻² Tor.
The pressure is reduced to about r and the object to be processed is cooled. The object to be treated may be cooled under reduced pressure, or may be introduced by introducing the above-mentioned replacement gas into the airtight container.

If the pressure in the airtight container is low, it takes time to cool the object to be treated and the takt time becomes long. Therefore, from the viewpoint of productivity, it is preferable to introduce the replacement gas for cooling.

By performing the heat treatment itself of the object to be treated under reduced pressure, it is more effective to reduce the concentration of the organic halide remaining in the heating residue of the object to be treated.

When the heat treatment is carried out under reduced pressure, and after cooling under reduced pressure and cooling without introducing a replacement gas, the heating residue is exposed to a non-oxidizing gas before being discharged into the atmosphere. Is preferred. This is because the object to be treated has a very large surface area due to heating under reduced pressure, and the surface free energy is likely to be in an excessive state, so if it is discharged into the atmosphere as it is, it may be ignited violently and may be dangerous. In particular, when the heating residue contains Mg, Al, and other metals, it is preferable to expose the heating residue to a non-oxidizing gas before discharging the heating residue into the atmosphere. (Embodiment 4) When the heating treatment and the cooling treatment of the object to be treated are carried out in the same airtight container, the object to be treated in the next batch cannot be introduced until the cooling of the heating residue of the object to be treated is finished. In order to realize continuous processing, the heating chamber and the cooling chamber may be separated by a heat insulating door and a vacuum door. Further, when the object to be treated is also heated under reduced pressure, a purge chamber may be arranged in front of the heating chamber.

For example, a purge chamber provided with a vacuum door may be provided at the inlet of the airtight region provided with the heating means and the pressure adjusting means. After the object to be treated is introduced into the purge chamber and the inside of the purge chamber is depressurized or purged with a replacement gas, the vacuum door to the airtight container for heat treatment is opened and the object to be treated is introduced into the airtight container. By adopting such a configuration, it is possible to introduce a new object to be processed even during the heat treatment of the object to be processed without mixing air or the like into the airtight container.

Further, for example, when the object to be treated is transported in the chamber without using the jig tray, two connected purge chambers may be arranged in the preceding stage of the vacuum heating chamber. Further, a jig such as a tray that can move between the two purging chambers and a charging device for the vacuum heating chamber may be provided. This tray may be moved back and forth between the two purge chambers by a transfer means such as a drawer or a pusher. Further, the object to be treated may be thrown into the vacuum heating chamber in a loose state. Then, the purge chamber on the side separated by the airtight container and the vacuum door may be decompressed to purge the air.

The removal of the heating residue of the object to be treated from the airtight container for the heat treatment can be similarly performed. Further, since it takes time to cool the heating residue, it is possible to improve productivity by circulating the tray. For example, at the outlet of the object to be processed of the airtight container, a storage chamber capable of hermetically storing the heating residue, a cooling chamber for cooling the heating residue, and a tray, a casing, or the like for heating the tray by replacing the atmosphere with a replacement gas. There are provided four chambers: a purge chamber for accommodating and purging the residue conveying means and a discharge chamber for discharging the heated residue to a conveyor or the like at normal pressure. Each of these four chambers may be equipped with a vacuum door so that it can be kept airtight independently. Then, the heating residue is conveyed by moving a jig such as a tray through these four chambers. In order to facilitate movement, these chambers may be provided in a grid shape (for example, each chamber is provided at each vertex of a quadrangle).

In order to convey the heating residue from the airtight container to be heat-treated to the storage chamber, the storage chamber may be provided below the airtight container in addition to various kinds of conveying means, and the heating residue may be dropped by gravity.

The heating residue of the object to be treated, which has been heat-treated in the airtight container, is moved to the outlet side in the airtight container by the conveying device for the object to be treated arranged in the airtight container. Then, it is transported to a storage chamber arranged adjacent to this outlet. A tray is waiting in the storage room, and the heated residue is stored in this tray. The tray and casing are then moved to the cooling chamber and the heated residue is cooled as described above. After cooling the heated residue, the tray is moved to the discharge chamber, and the heated residue is discharged from the discharge chamber to a conveyor or the like.

The empty tray from which the heating residue has been discharged is returned to the first storage chamber through the purge chamber for purging air. In this way, the tray can go around each room.

In this way, it is possible to perform a predetermined processing while circulating each chamber using a plurality of trays, and it is possible to improve the processing efficiency. Since it takes time to cool the heating residue in particular, such a cyclic treatment is effective.
The productivity can be further improved by disposing a plurality of cooling chambers in parallel between the first storage chamber and the discharge chamber.

The tray may be moved between the chambers by a transporting means such as a pusher or a roller. You may make it use combining several conveyance means.

By providing a chamber capable of decompression purging at the entrance and the exit of the object to be processed in the airtight container as described above, a new object to be processed can be introduced even while the object to be processed is heated. It becomes possible to remove the heating residue. As a result, operation can be automated and productivity can be improved. (Embodiment 5) Next, heat treatment, preheating, and
An example of processing of gaseous emission generated by purging, cooling, etc. will be described. Here, the gaseous emission is basically an exhaust gas emitted along with a heat treatment such as combustion or thermal decomposition of an object to be treated, but a solid or liquid substance mixed in the exhaust gas. Does not exclude cases including

The gaseous emissions of the object to be treated often contain organic halides such as dioxins. In addition, compounds derived from the object to be treated, such as water, oil, metals, metal oxides, etc., are included. Such substances need to be decomposed, removed or recovered before the gas is released into the environment.

The gaseous emission of the object to be treated is about 500.
By heating to about ° C to about 950 ° C, or about 500 ° C to about 1200 ° C, it is reformed and decomposed. This treatment is preferably performed in a reducing atmosphere.

At the time of this reforming, various catalysts for decomposing organic halides such as palladium oxide, ceramics such as honeycomb shapes, and metals such as aluminum are used to promote decomposition of the organic halides. May be.

Also, NaOH, Ca (OH)_TwoBy alkali such as
NOx and SO in gaseous emissions _X  Cl_TwoRemove
You may do it.

Further, since organic halides such as dioxins may remain in the reformed gas or may be resynthesized, it is necessary to provide a cooling device for cooling the reformed gas with a refrigerant such as water or oil. Good. This cooling is preferably performed by quenching so that the residence time of the gaseous effluent at the formation temperature of organic halides such as dioxins is as short as possible. Also, in order to prevent the formation of organic halides by reacting the halogen in the gaseous effluent with alkali, the refrigerant is made alkaline, the alkali auxiliary agent is mixed with the refrigerant, or the alkali is injected separately from the refrigerant. You may do it. The refrigerant may be injected into the gaseous emission by a gas ejector, Venturi, or the like. Further, since the gaseous emission may contain dust, it is preferable to provide a filter for removing these.

Therefore, the cooling device is equipped with a dust filter, an alkali tank, a heat exchanger, a pump and the like.

The gas that has passed through the cooling device is sent to a recovery device for condensing and recovering the residual condensate in the gas. In addition, in front of the exhaust pump that exhausts the inside of the processing system, an adsorption member such as an activated carbon filter should be installed in preparation for failure of each device for detoxifying the above-mentioned gaseous emission and overload. Is preferred. (Embodiment 6) Here, an example of the treatment of gaseous effluent when the heat treatment is performed under reduced pressure will be described.

The gaseous effluent of the object to be treated is reformed as described above. And the water contained in the gaseous emissions,
It is sent to a recovery device for condensing and recovering oil, evaporated metal, oxides and the like. Further, dust removal is performed by a filter for removing dust and the like still remaining in the gaseous emission, a cyclone, a liquid trap such as an oil trap, and the like.

In the gaseous effluent treatment system, the space between the collecting device and the dust removing device is kept airtight so that the condensate can be collected and the filter can be replaced during the heat treatment of the object to be treated. A vacuum door and a vacuum valve are provided for this purpose.

For taking out the condensate from the system, it is preferable to expose the condensate to a non-oxidizing gas after cooling it as described above and before discharging it to the atmosphere. This is because the surface area of the condensate is very large due to heating under reduced pressure, and the surface free energy easily becomes excessive. Therefore, if it is discharged into the atmosphere as it is, it may be dangerous because it may ignite violently, and in particular, metals such as Mg and Al may cause a fire, which is dangerous.

At the subsequent stage, an airtight container for heating the object to be treated under reduced pressure and a vacuum pump for reducing the pressure of the gaseous effluent treatment system are provided. As the vacuum pump, a booster pump, a rotary pump, a water ring pump or the like may be selected and used in combination as necessary. A pump for sucking the rear side of the vacuum pump may be provided.

Further, as described above, the organic gas in the gaseous emission is
Rogenide, NOx, SO_X  Cl _TwoCooling equipment to remove
You may make it equipped with a device. For failsafe
An adsorption device is preferably provided as well. (Embodiment 7) FIG. 7 schematically shows an example of the configuration of a processing apparatus of the present invention.
It is a figure showing roughly. This processing device is processed at almost normal pressure.
The elephant object is heated and the heating residue contains dioxin and other substances.
Which can prevent machine halide from remaining
is there.

FIG. 8 is a diagram schematically showing an example of the configuration of the processing apparatus of the present invention. This processing apparatus can heat an object to be processed under reduced pressure and prevent organic halides such as dioxins from remaining in the heating residue.

FIG. 9 is a diagram schematically showing an example of the configuration of the processing apparatus of the present invention. This processing apparatus is capable of continuous processing, and is the decompression-type processing apparatus illustrated in FIG. 8 equipped with an automatic charging device for an object to be processed and an automatic removal device for heated residues.

The atmospheric pressure type processing apparatus of FIG. 7 is lower in cost than the reduced pressure type processing apparatus. After the heat treatment of the object to be treated, this treatment apparatus replaces the atmosphere gas containing the organic halide with a substitution gas such as nitrogen, and cools the object to be treated in a state where the concentration of the organic halide in the atmosphere is reduced. As a result, the concentration of organic halide remaining in the heating residue can be reduced.

In the example of FIG. 7, the object to be treated introduced into the heat treatment furnace 103 through the inlet 101 is heated by the heater 105. In order to improve the temperature raising efficiency, a stirrer (not shown) may be provided to stir the atmosphere in the furnace or stir the object to be treated. The temperature in the furnace is controlled by the temperature sensor 107 and the control device 110b capable of controlling the heater.
Controlled by. The gas sensor 108 for detecting the gas concentration in the furnace is provided according to the type of gas to be detected such as oxygen concentration and chlorine concentration. The concentration of such a gas may be adjusted by introducing a carrier gas such as nitrogen or a rare gas.

After the object to be treated is heated in the heat treatment furnace 103, the valve of the replacement gas introduction system 106 is opened to introduce the replacement gas, and the organic halide in the atmosphere gas in the furnace is reduced and removed.

Then, the valve of the replacement gas introduction system 106 is closed and the gas cooling device 104 equipped with a filter, a gas cooler and a pump in the bypass is operated to cool the heating residue in the replacement gas atmosphere. After completion of cooling, the heating residue of the object to be treated is taken out from the outlet 102.

On the other hand, the gaseous effluent generated by heating is drawn into the decomposition reaction vessel 131, and the gaseous effluent emitted from the heating furnace 103 is reheated by heating with a heater to be thermally decomposed and reformed. Undecomposed gas is also decomposed.

In the decomposition reaction container 131, a spherical or honeycomb-shaped ceramic material, a catalyst, and a reducing agent (for example, Zn, Al, Mg, etc.) for promoting the thermal decomposition of the gaseous emission.
Etc., and an alkali agent for reacting and removing the decomposed gases NO _X , SO _X , Cl _{2 and the} like may be added. The ceramics, catalysts and reducing agents can be used alone or in combination depending on the gas conditions.

The gas exiting the cracking reactor 131 may still contain various hydrocarbons. This ingredient is
The condenser 111 condenses oil and water contained in the gaseous emission.

The filter 112 removes dust and the like from the gas that has passed through the condenser 111. A vacuum pump 114 such as a rotary pump is provided after the filter 112. It takes time to replace the gas in the heat treatment furnace 103 only by introducing the replacement gas, and a large amount of replacement gas is required, so that the amount of gas to be processed increases. Therefore, first, the heat treatment furnace 103 is evacuated by the vacuum pump 114,
Then, it is preferable to introduce a replacement gas, restore the pressure and cool.

The gaseous effluent of the object to be treated is passed through the filter 112 and the vacuum valve 113, and then the gas heating furnace 115.
Will be introduced to. About 7% of undecomposed gas, regenerated dioxin, residual dioxin, etc.
Decomposes and reforms at a high temperature of about 00 ° C to about 1100 ° C. The gas decomposed and reformed in the gas heating furnace 115 is cooled while being mixed by a cooling device 116 with a gas ejector and introduced into a cooling water tank 118 with an oil / water separation tank.
This cooling is preferably performed as rapidly as possible in order to shorten the residence time of the dioxin production temperature. For example, it is preferable to perform this cooling within 10 seconds. The cooling water passes through an alkaline tank 117 for controlling the water used for cooling to be alkaline, a pump, a heat exchanger, and a cooling device 11.
It is recycled to 6. Here, NO _X in the decomposition gas,
SO _X , Cl _2, etc. are also removed by reaction.

Also, in the cooling water tank 118 with the oil / water tank,
Condensates such as oil condensed by cooling are also collected.

Since the gas that has passed through the oil / water separation tank 118 may still contain dust and the like, the dust is removed by the filter 119, the bag filter 120 and the like. The dust trapped in the circulation system of alkaline water is filtered by the filter 13
It may be removed by 2.

A gas adsorbing device 121 is further provided at the subsequent stage of the bag filter 120 in case the gaseous emission of the object to be treated which has passed through the bag filter 120 contains harmful components which cannot be completely removed. . Then, the rear side of the adsorption device 121 is pulled by a suction pump 122 and exhausted. This exhaust gas is preferably discharged after monitoring the concentration of harmful components. Further, a bypass for circulating the exhaust gas to the gas heating furnace 115 may be provided. (Embodiment 8) Next, a decompression type processing furnace will be described with reference to FIG.

In this apparatus, the object to be processed can be processed in a larger amount than the manual decompression processing apparatus of FIG. 8 by the unmanned processing of the object to be processed.

Since the manual depressurization processing apparatus of FIG. 8 has many points in common with the depressurization type continuous apparatus, only different points will be described.

The object to be processed is transferred to the vacuum displacement chamber 302 by the conveyor 301, the upper vacuum door 303 is opened, and the transferred object to be processed is placed in the tray 304 (jig) in which it is installed, and the vacuum door 303 Close. afterwards,
The pressure in the substitution chamber 302 is reduced by the vacuum pump 305. continue,
The intermediate door 306 is opened to the next charging chamber 309 connected to the substitution chamber 302, and the object to be processed in the tray is moved to the charging chamber 309 by the transfer device 307.

Thereafter, the intermediate door 306 is closed and the charging chamber 30
Only the object to be treated is introduced into the heating furnace 310 by the introduction device 308 such as a rotating device disposed in the introduction chamber 309.

After the loading, the empty jig 304 opens the vacuum door 306 and is returned to the vacuum substitution chamber 302 by the transfer device 307b. Thereafter, the intermediate door 6 is closed, air is introduced into the vacuum displacement chamber 302, and the pressure is restored to normal pressure. After that, the upper door 303 of the vacuum displacement chamber 302 is opened and the next object to be processed is moved to the tray 304.
Throw in.

By repeating the above operation, the heating furnace 31
The object to be treated can be charged into the heating furnace 310 without mixing air into the heating chamber 310.

The object to be treated put in the heating chamber 310 is heated by the heater 311 and moved to the treatment outlet side by the screw conveyor 312. The temperature inside the furnace is controlled by the temperature sensor 313 and the heater controller 314. The gas sensor 313a is installed according to the type of gas.

The object to be treated, which is transferred while being heated in the heating furnace by the screw conveyor 312, drops onto the tray placed in the storage chamber of the outlet side outlet 315.
Then, when the number of drops reaches the set value, the screw conveyor 312 is stopped, then the vacuum door 317 to the next chamber is opened, and the conveying device 316 conveys it to the cooling chamber 318. After that, the vacuum door 317 is closed.

The transported object to be treated is cooled by a gas cooling device 321 which circulates a cooling gas such as nitrogen.

During this cooling, the empty tray placed in the vacuum displacement chamber 323 is opened with the intermediate door 322a, and the transfer device 3 is opened.
It is conveyed to the storage chamber 315 by 24.

Thereafter, the vacuum door 322a is closed and the screw conveyor 312 is rotated. During this time, the vacuum valve 332 is opened in the vacuum replacement (purge) chamber and air is introduced to restore the pressure.

The object to be treated cooled in the cooling chamber 318 opens the exit side vacuum door 322 in the right-angled direction, and the transfer device 31.
At 9, it is carried onto the conveyor 326. Then the vacuum door 322
Is closed and the pressure is reduced by the vacuum pump 320.

The object to be processed on the conveyor 326 is conveyed to the rotary charging chamber 327, and only the object to be processed is charged on the take-out conveyor 329 by the rotating device 328.

The empty tray after loading is the transport device 330.
Then, the vacuum door 331 is opened, and the vacuum door 331 is sent to the vacuum purge chamber 323. Thereafter, the vacuum door 331 is closed and the vacuum pump 325 depressurizes the vacuum replacement chamber.

With such a structure, the heating residue of the object to be treated can be taken out from the heating furnace while keeping the heating furnace airtight.

The difference between the manual decompression furnace and the continuous decompression furnace is the difference between manual and automatic loading and unloading of the object to be treated. The continuous furnace at the heating furnace inlet and outlet is a vacuum displacement chamber, charging chamber, storage chamber, There is a cooling room. Further, in the manual decompression furnace, cooling is performed in the heating furnace. (Embodiment 9) Next, the processing of the gaseous emission discharged from the heating furnace 310 will be described with reference to FIG.

The gaseous effluent generated by heating the object to be treated is drawn into the decomposition reaction chamber 332 connected to the heating furnace 310 and reheated including undecomposed components to be thermally decomposed and reformed.
Then, as described above, the ceramics, the catalyst and the reducing agent are charged into the decomposition reaction chamber 332 to accelerate the decomposition of each gas. Further decomposed NOx in the gas, introducing the alkaline agent in order to remove harmful gases such as SO _X Cl _2.
The above-mentioned decomposition-promoting alkaline agents are used alone or in combination depending on the gas conditions.

The heating furnace 31 is provided downstream of the decomposition reaction chamber 332.
There is a vacuum door 333 that seals 0 and the decomposition reaction chamber 332.
The gaseous emission that has passed through the decomposition reaction chamber 332 is
It is led to a recovery device 334 which can condense and recover water, oil, metals, and oxides contained in the gaseous effluent. Furthermore, the Sakuron 335 and the filter 336 which remove the dust in the gas and the filter 336 oil liquid trap 33
Guided to 7. A vacuum valve 338 that seals the space between the vacuum door 333 and the oil-liquid trap 337 is installed at the subsequent stage of the oil-liquid trap 337. This vacuum valve 33
8. Due to the double sealing by the vacuum door 333, it is possible to condense and collect evaporants derived from the object to be treated and replace the filter during operation. Also, as mentioned above,
If a cooling gas such as nitrogen is circulated through the recovery device to cool it, the recovery time is short and fire is unlikely to occur.

After the vacuum valve 338, a decompression device 339 such as a rotary pump, a booster pump, a water ring pump with an ejector, etc. for decompressing the above-mentioned processing system and a decompression device are connected, and residual dioxins, NOx, S and S in the gas are connected.
A pollution gas removing device 340 for removing other pollution gas such as O _X Cl ₂ is provided. The pollution gas removing device 340 for removing the pollution gas heats the gas at a high temperature with a heater, mixes the gas into the ejector cooling device within about 10 seconds and rapidly cools it to prevent re-synthesis of the organic halide. The device may use the ejector system as described above. It is preferable that the water used is made alkaline and circulated, and mixed with the above-mentioned gas to form harmful components. Further, other methods such as dry decomposition such as plasma decomposition, corona discharge decomposition and glow discharge decomposition may be used.

The gas discharged from the pollution gas removing device 340 is introduced into the adsorbing device 341 which adsorbs the remaining pollutant gas and the adsorbing device 341 which adsorbs the remaining polluting gas and sucks the gas of the device after the vacuum pump 339. (Embodiment 10) The present invention is applied to treat shredder dust. We made automobile shredder dust as a sample. This sample consists of the following six types of fractions. The automobile used was a Minica (manufactured by Mitsubishi Motors Corporation).

(1) Vinyl chloride (10 wt%) (2) Polypropylene (10 wt%) (3) Polyurethane (10 wt%) (4) Rubber (10 wt%) (5) Polyurethane (10 wt%) (6) Others (50 wt %) The fraction of (6) was pressed. Such shredder dust is pyrolyzed at atmospheric pressure (600 ° C, 80
0 ° C.) and vacuum pyrolysis (600 ° C., 800 ° C.), and the concentration of dioxin contained in the pyrolysis residue was measured.

FIG. 11 is a diagram for explaining processing conditions for thermal decomposition. In the case of 600 ° C., the temperature was raised from room temperature to 600 ° C. in 2 hours, kept at 600 ° C. for 2.5 hours, and then cooled. In the case of 800 ° C., the temperature was raised from room temperature to 800 ° C. in 2.5 hours, and the temperature was maintained for 2.15 hours and then cooled. In the case of cooling under reduced pressure pyrolysis, the reduced pressure substitution of the present invention was applied, but in the case of cooling under atmospheric pressure pyrolysis, air cooling was performed without applying the present invention. Further, the thermal decomposition residue at 800 ° C. under atmospheric pressure where dioxin remains was further thermally decomposed under reduced pressure at 800 ° C., and the concentration of dioxin contained in the thermal decomposition residue was measured (800 in the figure).
℃ pyrolysis B fraction).

FIG. 12 shows the measurement result. Measurement is PCDD
s and PCDFs were performed separately, and the sum of them was used as the dioxin concentration (ng / g). In addition, n. d. (Not d
indicated that dioxin was not detected.

As described above, according to the present invention, dioxins in the heating residue can be significantly reduced. Especially in the thermal decomposition under atmospheric pressure, dioxin remains even after the treatment at 800 ° C., but when the residue is retreated under reduced pressure, the dioxin can be removed. Here, an example of the process in which the shredder dust is used as the object to be processed has been described, but similar results can be obtained in the case of soil, incinerated ash, sludge and the like. The present invention may be used as a waste treatment apparatus as a manual type suitable for small-scale treatment for general factories, or as a continuous treatment furnace suitable for large-scale treatment in municipalities, etc., and can be combined depending on the treatment cost. (Embodiment 11) FIGS. 13, 14, 15, and 16 are diagrams schematically showing another example of the configuration of the processing apparatus of the present invention.

In FIGS. 13, 14, and 15, two heating chambers, a dry distillation chamber 701 for atmospheric pyrolysis and a vacuum evaporation chamber 702 for vacuum pyrolysis, are provided. Further, a cooling chamber 703 for cooling the heating residue is arranged in the subsequent stage. These processing chambers are separated by a vacuum door so that they can be opened and closed.

In the configurations illustrated in FIGS. 13, 14 and 15, an object to be treated such as soil is introduced into the carbonization heating chamber 701 and thermally decomposed, and then introduced into the vacuum evaporation chamber 702 such as arsenic and cadmium. Heavy metals such as lead are removed by evaporation. Then, the heating residue of the object to be treated is introduced into the cooling chamber 703 and cooled in the same atmosphere as described above, which is free of organic halide and does not have the ability to generate organic halide. The exhaust of the system is performed by booster pumps 705 and 712 and rotary pumps 706 and 713. The processing of the gaseous effluent of the object to be processed is performed by the gas processing device as described above.
The gaseous effluent from the dry distillation heating chamber 701 is introduced into the gas treatment device 714 via a gas cracking device 707 and a condenser 708 for condensing and recovering the vaporized substances in the gaseous effluent. The gaseous emission from the vacuum heating chamber 702 is introduced into the gas processing device 714 via the condenser 709 and the oil filter 711. Gas treatment device 714
Is a gas cracking device 715, a jet scrubber 7
16, equipped with an activated carbon filter and an exhaust blower 718. Further, in the example of FIG. 15, the gas cracking device 715 is omitted in the gas processing device 714. Further, a gas combustion device that burns the gaseous emission may be provided instead of the jet scrubber 716, and an alkaline shower that cleans the gaseous emission with an alkali may be provided instead of the activated carbon filter 717.

13 and 15, the dry distillation heating chamber 70 is shown.
The loading chamber 704 for introducing the object to be treated and the dry distillation heating chamber are common to each other, but they may be provided separately. Further, in FIG. 15, an oil jet scrubber 708b is provided as a gas treatment device, and the oil content in the gaseous emission is collected here, but a condenser 708 may be provided.

FIG. 16 is a diagram schematically showing another example of the configuration of the processing apparatus of the present invention.

The example of FIG. 16 is an example of the processing apparatus of the present invention which can be added to a refuse incinerator that has been conventionally used in local governments and the like. Here, a configuration is exemplified in which the removal processing of the heating residue from the heating furnace is performed in the same manner as the input operation on the inlet side in FIG. With such a configuration, the concentration of organic halides such as dioxin contained in the incineration residues of various wastes can be reduced.

Also in the processing apparatus illustrated in FIGS. 15 and 16, a plurality of cooling chambers may be provided in parallel, like the processing apparatus of the present invention described above. As a result, productivity can be improved even when it takes time to perform the processing in each room. In addition, a plurality of trays may be introduced into each chamber for processing. (Embodiment 12) FIG. 17 is a diagram showing an embodiment of the present invention in a single furnace configuration. The decompression furnace 1 is provided with a control device 2 and a constant temperature halogen removing device 4 via a vacuum door 3 which is normally arranged in double. The decompression furnace 1 is a steaming furnace (pyrolysis furnace) equipped with heating means whose temperature is controlled by the control device 2. The vacuum pump 5, which is an exhaust system, keeps the atmospheric pressure at a predetermined degree of vacuum while abandoned a vehicle or the like. The object to be processed is steamed (pyrolysis).

[0209] A constant temperature halogen removing device (constant temperature chloride removing device) 4 which is a means for removing halogen such as chlorine contained in the gaseous emission is a chamber into which the evaporative gas from the decompression furnace 1 is introduced, and the room temperature is It is set to a predetermined value of about 400 ° C to about 1000 ° C. Further, in this example, the constant temperature halogen removing device 4 is composed of two chambers, and in the first chamber 4a, a metal such as iron that reacts with chlorine in the gaseous effluent to form chloride, Dalai powder and / or A compound such as calcium hydroxide is loaded. In addition, a catalyst that accelerates the fixing reaction of halogen in the gaseous effluent and the decomposition of the organic halide in the gaseous effluent is loaded.

The second chamber 4b is a chamber for adsorbing halogen that has passed through the first chamber 4a, and is loaded with an adsorbent such as zeolite such as spherical zeolite or activated carbon. In the constant temperature halogen removing device 4, it is preferable to maintain the temperature as low as possible in order to enhance the adsorption effect and adsorption efficiency of the adsorbent. The gaseous effluent that has passed through the first chamber 4a is cooled in the second chamber 4b, but this cooling keeps the temperature of the gaseous effluent within the regeneration temperature range of organic halides such as dioxins. It is preferred to do it rapidly so that the residence time is as short as possible.

As described above, the constant temperature halogen removing device 4 heats the gaseous emission containing the evaporative gas when the vacuum degree in the decompression furnace 1 does not reach the set value due to the breakdown of the equipment, the structure of the object to be treated, or the like. However, while dechlorinating the dioxin contained in the gaseous effluent, chlorine reacts with metallic Dalai powder, calcium hydroxide, etc. to fix as chloride, and chlorine that does not react further and tries to flow out It plays a role of adsorbing and removing the adsorbent.

Between the constant temperature halogen removing device 4 and the vacuum pump 5, a condenser device (condenser) for condensing and recovering metal, water, oil, oxides and the like contained in the gaseous emission is recovered. ) 6 is installed. The condenser 6 condenses and collects metals, water, oil, oxides, etc. contained in the gaseous emission. If necessary, the condenser 6 may be installed in a plurality of systems.

Thereafter, the vaporized gas is sent to a removing device 7, which is a filter for removing SOx and the like in the gaseous emission, which is installed in the latter stage of the vacuum pump 5, and there, NOx, chlorine, NH ₃ (ammonia) and After SOx is removed and rendered harmless, it is discharged to the outside of the system. The removing device 7 includes, for example, honeycomb-shaped zeolite, activated carbon, and other adsorbents. (Embodiment 13) FIG. 18 is a view showing an embodiment of the continuous furnace configuration of the present invention. The processing apparatus illustrated in FIG. 18 is basically a continuous furnace configured by connecting the pressure reducing furnaces 1 illustrated in FIG. In this case, for example, in heating furnaces installed in series, the thermal decomposition temperature in each furnace is set to gradually increase.

For example, in the first furnace 1a, which is a preheating chamber, for example, soil, sludge, agricultural products, marine products, plastics, fibers, rubbers, metals, metal oxides and the like to be treated under normal pressure at about 0 to 100 ° C. By heating in the range, mainly water and oil are evaporated from the object to be treated.
In the second furnace 1b, which is a replacement chamber for replacing the atmosphere in the furnace to a non-oxidizing atmosphere, the inside of the furnace is about 1 to 500 Torr.
The residual oil and halogens such as chlorine are mainly evaporated from the object to be treated by maintaining the temperature to some extent and heating in the range of about 100 to 160 ° C. Dioxins are not produced under the temperature condition of about 180 ° C. or below, so it is necessary to evaporate as much water as possible, vaporizable organic components such as oil and halogens such as chlorine at this stage in order to reduce organic halides. Is preferred. With such a configuration, pressure control in the pressure reducing furnace at the subsequent stage is not burdened. Further, it is possible to reduce the possibility that harmful organic halides such as dioxins are produced.

[0215] Further, since dioxins are not generated in the first furnace 1a and the second furnace 1b which are maintained at a relatively low temperature, in an evaporative substance (including gaseous effluent) treatment system connected to them, Constant temperature halogen removal device 4 described above
It is also possible to omit the provision of halogen traps such as.

In the third furnace 1c, the degree of vacuum is about 10 ^-1 to about 1.
It is held at 0 ⁻⁴ Torr and heated in a range of about 180 to 400 ° C. to thermally decompose an object to be treated such as soil, sludge, agricultural products, marine products, plastics, fibers, rubbers, metals, metal oxides. Then, in the fourth furnace 1d, the degree of vacuum is maintained at about 10 ⁻² to about 10 ⁻⁶ Torr, and the object to be treated is heated in the range of about 400 to about 1400 ° C. Further, the ends of the evaporative substance treatment lines installed in each of the furnaces 1a to 1d are individually or collectively collected and directed to the outside of the apparatus, from which the pollution-free evaporative gas is discharged to the outside of the system.

A cooling settling chamber 8 is provided adjacent to the final stage fourth furnace 1d. The inside of the cooling condensing chamber 8 is heated to 50 to 200 with a water cooling pipe or other heat exchange device under reduced pressure.
The evaporative gas flowing from the fourth furnace 1d, which is kept at a low temperature of ℃, is cooled to condense the evaporant from the object to be treated and protect the inlet vacuum packing of the cooling / air displacement chamber 9.

The air replacement chamber 9 is installed adjacent to the cooling condensing chamber 8 and is supplied with nitrogen gas under normal pressure in the same manner as the cooling condensing chamber 8.
It is cooled to a low temperature of about 0 ° C. After the object to be treated is sufficiently cooled in the room, the object to be treated is taken out in the air displacement chamber 9.

The above-mentioned treatment method and treatment apparatus include, for example, a heating residue, incineration fly ash, containing organic halides such as dioxins from a municipal waste treatment facility or a factory.
For treating objects such as residual ash or residual liquid, as well as objects such as soil containing organic halides such as dioxins by pouring from garbage treatment facilities, waste treatment facilities, factory chimneys, etc. Can also be applied.

As described above, the present invention is capable of evaporating water, oil, chlorine and the like in the initial treatment stage in which dioxin is not generated by performing thermal decomposition treatment of a scrap car while changing both the treatment pressure and temperature in the heating chamber. it can. Therefore, the amount of vaporized gas generated in the subsequent processing stage can be suppressed, and pressure control becomes easy. Further, since the temperature inside the room is also raised stepwise, it is possible to smoothly carry out the thermal decomposition of a scrap car or the like.

In addition to the above, the method and the treatment apparatus according to the present invention are also applied to, for example, heating residues, incinerated fly ash, residual ash, or dioxins contained in residual liquid from municipal waste treatment facilities and factories. can do.

Further, according to the present invention, even if the inside of the decompression furnace does not reach a predetermined vacuum degree due to equipment failure or the like,
It is possible to sufficiently achieve dechlorination of the evaporative gas and prevent dioxins from being produced.

[0223]

The present invention is as described above, and from the viewpoint that it is effective to control the amounts of reactive chlorine atoms and oxygen in order to suppress the production of dioxins, the decomposition gas generated by thermal decomposition. Is introduced into the reduction retort to remove chlorine and oxygen, and the concentration of oxygen and chlorine in the gas discharged from this reduction retort is analyzed. The adjustment is performed, and it is possible to suppress the generation of dioxin at the time of thermal decomposition and to surely perform the decomposition and removal of the generated dioxin or the residual ash, dioxin remaining in the soil or the like.

Further, in the present invention, by carrying out the thermal decomposition under reduced pressure, it is possible to more efficiently suppress the generation of dioxin,
Decomposition processing becomes possible, and in this case, by using a water ring pump as a vacuum pump, there is an effect of enabling thermal decomposition processing in which a large amount of water such as household waste and shredder dust is generated.

Further, a gaseous effluent generated by thermal decomposition is subjected to a step of collecting evaporated metal by condensation, a step of removing powder with an oil film, a step of generating salts by contact with an alkaline solution, and a step of removing salts with an ion exchange resin film. When it is processed after that, there is an effect that the removal of dioxin becomes more reliable.

In the present invention, the heating residue of the object to be treated is cooled after removing the organic halide-containing gas such as dioxin so that the heating residue does not contain an organic halide such as dioxin. You can

By adding the treatment apparatus of the present invention after the conventional combustion furnace or waste treatment furnace for waste treatment, it is possible to effectively reduce dioxin and the like in the heating residue.

Further, the residual dioxin can be removed from the soil containing dioxin, the heating residue such as incinerated ash, and the sludge, water, oil and the like flowing out from these by using the above invention.

Furthermore, the present invention can reduce not only the heating residue but also harmful substances in the gaseous emission from the object to be treated. In addition, by providing multiple measures for harmful substances in the gaseous effluent treatment system, safe and reliable treatment can be performed.

Also, a method different from the gas replacement method in which a reducing substance is charged into the furnace during heating to reduce and remove dioxins in the gaseous emission and then the heating residue is cooled has been realized. They may be used in combination.

[Brief description of drawings]

FIG. 1 is an overall configuration diagram of an embodiment of the present invention.

FIG. 2 is a configuration diagram of a main part of the embodiment of the present invention.

FIG. 3 is a configuration diagram of an oil powder trap according to an embodiment of the present invention.

FIG. 4 is a configuration diagram of main parts of another embodiment of the present invention.

FIG. 5 is an overall configuration diagram of still another embodiment of the present invention.

FIG. 6 is a dioxin generation system diagram estimated by Chowdry et al.

FIG. 7 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 8 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 9 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 10 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 11 is a diagram for explaining processing conditions of a processing target object.

FIG. 12 is a diagram showing a measurement result of residual dioxin concentration of a heating residue.

FIG. 13 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 14 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 15 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 16 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 17 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

FIG. 18 is a diagram schematically showing an example of the configuration of a processing apparatus of the present invention.

[Explanation of symbols]

1 Pyrolysis furnace 2 controller 3 collection device 5 sensors 18 Object to be processed 20 Heating means 21 Cooling means 40 vacuum valve 41 booster pump 47 Water ring pump

─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. ⁷ Identification code FI theme code (reference) C02F 11/00 F23G 7/14 C07B 35/06 B09B 3/00 303A C07D 319/24 303C F23G 7/00 303E 7/14 303H 303L 303M 303P 303Z B01D 53/34 134E 136A 136Z (72) Inventor Yasuo Mishima 66 Tsujimachi Teraike, Toyota City, Aichi Prefecture Toyohei Shokai Co., Ltd. (72) Katsuo Takamiya Tsutsumachi Town, Toyota City, Aichi Prefecture 66 Teraike F-house in Hoei Shokai Co., Ltd. (reference) 2E191 BA12 BB01 BC01 BD11 BD13 4D002 AA02 AA12 AA17 AA18 AA28 AA29 AC10 BA02 BA06 BA12 BA13 BA14 CA01 DA02 DA05 DA06 DA08 DA11 DA12 DA21 DA35 DA70 EA02 FA02 FA02 GA02 GA03 GA02 GA03 GB06 4D004 AA02 AA04 AA07 AA22 AA28 AA36 AA41 AA46 AB03 AB06 AB07 AC05 CA22 CA32 CB09 CB32 CB45 CC01 DA02 DA06 4D059 AA09 AA12 AA14 AA30 BD01 BD12 BD32 CA14 EB06 EB08 4H006 AA05 AC13 BC10 BC11 BD84

Claims (9)

[Claims] 1. A step of heating an object to be treated containing an organic halide and a heavy metal under a reduced pressure, a step of heating a gaseous emission generated by this heating under a reduced pressure, and a step of heating the object to be treated by the heating. And a step of condensing the evaporated heavy metal. 2. The processing method according to claim 1, wherein the heating step and the condensing step are performed in an exhaust system for decompressing a space for heating the object to be processed. 3. An airtight region capable of holding an object to be treated containing an organic halide and a heavy metal in an airtight manner, and at least a part of the organic halide is thermally decomposed, and at least a part of the heavy metal is evaporated. Thus, the means for decompressing and heating the airtight region, the means for heating under reduced pressure the gaseous effluent generated by the heating, and the heavy metal evaporated from the object to be treated by the heating is condensed under reduced pressure And a processing unit. 4. The processing apparatus according to claim 3, further comprising an exhaust system for decompressing the airtight region, wherein the means for heating the gaseous exhaust under reduced pressure decompresses in the exhaust system. And a heating device. 5. The heating residue of the object to be treated is cooled after the inside of the hermetically sealed region is replaced with a replacement gas that is substantially free of the organic halide and does not have the ability to form an organic halide. Item 5. The processing device according to item 3. 6. A second soil containing a heavy metal in a first concentration and an organic halide in a second soil containing the heavy metal in a second concentration lower than the first concentration. In the method of producing a soil, the first soil is introduced into an airtight region, and at least a part of the organic halide is thermally decomposed by heating the first soil under reduced pressure,
A method for producing soil, characterized in that at least a part of the heavy metal is evaporated, the gaseous effluent generated by the thermal decomposition is heated under reduced pressure, and the evaporated heavy metal is condensed under reduced pressure. 7. The method for producing soil according to claim 6, wherein the organic halide is dioxins. 8. The method for producing soil according to claim 6, wherein the halogen concentration in the gaseous effluent generated by the thermal decomposition of the soil is reduced. 9. The thermal decomposition residue of the first soil is cooled after the inside of the airtight region is replaced with a replacement gas that is substantially free of the organic halide and does not have the ability to form an organic halide. The method for producing soil according to claim 6.