The present invention relates to an oil reconversion device for recycling waste plastics.
Japanese Unexamined Patent Publication 2003-96469 discloses a conventionally known waste plastics oil reconversion device which reconverts waste plastics (high-polymer wastes) heavy oil (Grade-A heavy oil equivalent) after thermally cracking it by heating.
The oil reconversion device is equipped with a melting bath which has a first crucible placed inside a first coil, induction-heats the first coil by feeding a high-frequency current through the first coil, and melts solid waste plastics such as polyethylene, polysterol, and vinyl chloride contained in the first crucible at around 250° C. (70° C. for vinyl chloride), which is a relatively low temperature to obtain a molten plastic, and a thermal cracking bath which has a second crucible placed inside a second coil, induction-heats the second crucible by feeding high-frequency current through the second coil, and thermally cracks the molten plastic contained in the second crucible by heating it to a high temperature of around 450° C. (170° C. for vinyl chloride) to generate a cracker gas, which when cooled obtains a heavy oil.
However, the following problems remain to be solved for such a waste plastics conventional oil reconversion device.
First, because the waste plastics inside the first crucible to be induction-heated are heated as it is being agitated, its melting performance is limitated and is insufficient from the viewpoint of rapid melting and further homogeneous and high-quality melting.
Second, because construction is adopted wherein the bottom of the first crucible and the bottom of the second crucible are connected through a communicating tube, in which an open/close valve is installed, the manufacturing process becomes complex, making cleaning and maintenance difficult when the communicating tube is clogged.
Third, because it is equipped with two melting baths and a thermal cracking bath, although fit for processing a large amount of waste plastic, in processing small amounts of waste plastic, the large scale of the overall device may lead to a decrease in installability and universal usability, increasing running costs due to increased unnecessary power consumption.
The present invention has the objective of providing an oil reconversion device for waste plastics solves such problems of the background technology.
In order to solve these problems, the present invention is characterized in constructing oil reconversion devices 1a and 1b for waste plastics which thermally crack waste plastic Ro by heating it and converting a generated cracker gas Gr into oil by cooling, and is equipped with a thermal cracking bath 2 which has a bath main body 4 placed inside a coil 3 . . . , induction-heats the bath main body 4 by feeding high-frequency current through the coil 3 . . . , and thermally cracks at least the molten plastic Rd obtained from a waste plastic Ro to generate the cracker gas Gr, an injection port 5 through which the waste plastic Ro is injected, a feeder 6 which supplies the waste plastic Ro injected through the injection port 5 to the thermal cracking bath 2 via a forced or direct feeding means Ua or Ub without a bath, and an oil conversion processor 7 which cools and converts the cracker gas Gr generated by the thermal cracking bath 2 into oil.
The best embodiment forms of the present invention are explained in detail hereafter, based on the drawings.
First, the construction of an oil reconversion device 1a for waste plastics of the first embodiment form of the present invention is explained referring to
Shown in
The extruder 8 constitutes a feeder 6 as a forced feeding means Ua which melts and extrudes the waste plastic Ro injected through the injection port 5, is equipped with a heating cylinder 8c with a heater 21 . . . installed on its outer circumference, and has an extruding nozzle 22 on the front end of the heating cylinder 8c and a hopper 23 the top end of which becomes the injection port 5 on the rear section. The heating cylinder 8c contains an extruding screw 8s. The extruding screw 8s is rotationally driven by a screw rotation driver 24 installed on the rear end of the heating cylinder 8c. No. 25 represents multiple cooling blowers which cool the heating cylinder 8c 26 is an extruder controller, 28 is a machine stage having multiple legs 27, and F is a frame of the oil reconversion device 1a.
On the other hand, 29 represents a waste plastic pre-processor for obtaining the waste plastic Ro injected into the hopper 23 of the extruder 8. Contained in the waste plastic reprocessor 29 are a separation process to separate waste materials, a crushing process to crush the waste plastic Ro, a washing process to wash the crushed waste plastic Ro, a drying process to dry it, etc. The waste plastic Ro obtained through such pre-processing, is injected into the hopper 23 by a waste plastic injection means such as a conveyer 30, shown in
On the other hand, the tip port of the extruding nozzle 22 connects to the entrance port of a three-way valve 31 via an air line Pa as shown in
Shown in
As shown in
Also, an agitating mechanism unit 11 is installed in the thermal cracking bath 2. The agitating mechanism unit 11 is equipped with an agitate-scraping unit 12 placed inside the bath main body 4 and a rotation driver (driving motor) 34 installed on the outer upper end of the bath main body 4. In the center of the agitate-scraping unit 12 is a shaft 35 which is rotated by the rotation driver 34. As shown in
Installed on a shaft 35 positioned above the scraping blades 37p and 37q are heaters 13a and 13b which heat the top surface of the molten plastic Rd contained in the bath main body 4. As shown in
On the other hand, a gas exit port 38 for the cracker gas Gr is installed on the ceiling 4u of the bath main body 4, and this gas exit port 38 connects to the receiving side of the oil conversion processor 7 described later via an air line Pp. Furthermore, installed on the ceiling 4u is a catalyst injector, not shown, which feeds a catalyst such as zeolite which promotes thermal cracking into the bath main body 4. No. 39 is a safety valve.
The thermal cracking bath 2 constructed in this manner is supported at a specified height by a frame F as shown in
The oil conversion processor 7 cools the cracker gas Gr supplied via the air line Pp from the thermal cracking bath 2 and the cracker gas Gr supplied via the air line Pq from the residue processing bath 52 and converts them into oil, wherein the air lines Pp and Pq connect to the entrance port of a three-way valve 61. Also, one exit port of the three-way valve 61 connects to the entrance of a condenser 62, and the other exit port of the three-way valve 61 connects to the entrance of a condenser 62 via a gas reforming unit 63, which functions to crack terephthalic acid generated in large quantities when polyethylene terephthalate (PET) molded forms such as PET bottles are thermally cracked. Because the gas reforming unit 63 can be selectively connected, if no PET molded form is processed, the air lines Pp and Pq may be directly connected to the entrance of the condenser 62, or if only PET dedicated molded forms are processed, a dedicated system may be made which directly connect the air lines Pp and Pq to the receiving side of the gas reforming unit 63.
The gas reforming unit 63 prevents the inconvenience that, when terephthalic acid generated by thermal cracking of PET molded forms is supplied to the condenser 62, it accomplishes crystallization by cooling the condenser 62, generating pipe clogging etc. of a heat exchanger tube inside the condenser 62, and converts terephthalic acid by vapor-phase cracking into a low boiling point compound which does not crystallize. The principle construction of the gas reforming unit 63 is shown in
On the other hand, the condenser 62 functions to cool and convert the cracker gas Gr into oil, wherein the cracker gas Gr is cooled (heat exchanged) with cooling water W circulated from a cooling unit 65. Also, no. 66 is an oil storage tank, in which heavy oil obtained from the condenser 62 is stored. Because water is generated in the condenser 62, in which, in addition to heavy oil, an oil-water separation bath and a filter which separate heavy oil and water are built.
It is further equipped with the off-gas processor 16. As shown in
Other than the above, 81 is a high-frequency generation unit, which becomes a power supply unit to feed a high-frequency current to coils 3 . . . , 55, 76, and 95. Also, 82 is a nitrogen gas feeder, which prevents the cracker gas Gr etc. from making direct contact with air by feeding nitrogen gas into the bath main body 4, the bath main body 54, the water seal bath 92, the oil storage tank 66, etc. before opening them to the atmosphere.
The entire operation of the oil reconversion device 1a of the first embodiment form is explained hereafter, according to the flow chart shown in
First, in the extruder 8, the extruding screw 8s rotates by the screw rotation driver 24. Also, the heating cylinder 8c is heat controlled to approximately 300° C., necessary for melting the waste plastic Ro by the heater 21 . . . . The heating cylinder 8c is heated by the heater 21 . . . , and cooling is performed by the cooling blower 25 . . . .
During operation, the waste plastic Ro is injected into the hopper 23 of the extruder 8, in which case, the waste plastic Ro supplied to the extruder 8 is obtained by the waste plastic pre-processor 29. Namely, in the waste plastic pre-processor 29, collected waste materials are separated, during which mixed foreign materials (metals etc.) are removed (Step S1). Also, the waste plastic Ro obtained by the separation is crushed by a crushing unit creating chips of a specified size or smaller (Step S2). Furthermore, the crushed waste plastic Ro is washed by a washer and dried by a dryer (Step S3), after which dried waste plastic Ro is injected into the hopper 23 by a waste plastic injection means such as the conveyer 30 (
The waste plastic Ro contained by the extruder 8 is sufficiently melted inside the heating cylinder 8c to become molten plastic Rd and is extruded from the extruding nozzle 22 by the rotating extruding nozzle 22 (Step S5). In so doing, if the waste plastic Ro to be processed is a waste plastic Ro of other than vinyl chloride, it is supplied to the interior of the thermal cracking bath 2 from the feeding port 33 via the air lines Pa and Pb (Px) by switching the three-way valve 31.
Conversely, in the case of vinyl chloride, before feeding to the thermal cracking bath 2, processing is performed by the vinyl chloride processor 41, in which case the molten plastic Rd extruded from the extruding nozzle 22 by switching the three-way valve 31 is sent to the receiving side of the vinyl chloride processor 41 via the air line Pc. By this means, in the vinyl chloride processor 41 shown in
On the other hand, the thermal cracking bath 2 has the bath main body 4 induction heated by a high-frequency current fed to the coils 3 from a high-frequency generation unit 81. In so doing, the bath main body 4 is heated to about 450° C., necessary for thermally cracking the molten plastic Rd. The bath main body 4 is heated to about 200° C. while standing by. The heating temperature of the bath main body 4 can be arbitrarily set according to the kind of the molten waste plastic Ro to be processed. Therefore, in the thermal cracking bath 2, the supplied molten plastic Rd is heated to set a high temperature of about 450° C. to thermally crack the molten plastic Rd (Step S6).
Also, in the thermal cracking bath 2, the shaft 35 is rotated by the rotation driver 34 in the agitating mechanism unit 11 to agitate the molten plastic Rd contained in the bath main body 4 with the agitating blades 36p and 36q of the agitate-scraping unit 12, and the molten plastic Rd adhering to the inner wall 4w of the bath main body 4 is scraped off by the scraping blades 37p and 37q. By this means, easy and sufficient agitation to the molten plastic Rd can be performed, and the melting efficiency of the molten plastic Rd enhanced. Because the scraping blades 37p . . . was constructed by stacking three pieces of stainless-steel plates Ca, Cb, and Cc of different projection lengths, residue plastic Rd such as sediment adhering to the inner wall 4w of the bath main body 4 can be securely scraped off, preventing the degradation of thermal conductivity due to the residue plastic Rd adhering to the inner wall 4w.
Also, the heaters 13a and 13b also rotate simultaneously by the shaft 35 rotating, and the top surface of the molten plastic Rd contained in the bath main body 4 is heated at a high temperature of about 400˜500° C. By this means, thermal cracking of the molten plastic Rd near the top surface can be efficiently and effectively performed. Especially, because the top surface of the molten plastic Rd becomes a paste bubble state, it is heated by the heaters 13a and 13b to promote secondary cracking. On the other hand, in the thermal cracking bath 2, by the thermal cracking of the molten plastic Rd, the cracker gas Gr is generated, and supplied to the receiving side of the oil conversion processor 7, described later, via the air line Pp from the gas exit port 38 installed on the ceiling 4u. In this case, if the waste plastic Ro to be processed is other than PET molded forms, the cracker gas Gr is directly supplied to the condenser 62 by switching the three-way valve 61. In the condenser 62, heavy oil (Grade-A heavy oil equivalent) is generated by cooling (heat exchanging) the cracker gas Gr (Step S7), and the condenser 62 is always cooled with cooling water W from the cooling unit 65. Then, the obtained heavy oil is stored in the oil storage tank 66 (Step S8).
Conversely, if the waste plastic Ro to be processed is a PET molded form, the cracker gas Gr is sent to the gas reforming unit 63, in which gas reforming processing is performed (Step S9). In the gas reforming unit 63, an appropriate amount of water W supplied from the water content adjustment unit 72 is added to the cracker gas Gr by the mixer (scrubber) 71 by the supplied cracker gas Gr containing terephthalic acid. In this case, water W is mixed as water vapor. The cracker gas Gr which passed through the mixer 71 is supplied to the cracking bath 73, and passes through the catalyst 75 employing an acid (silica alumina) or a base (calcium oxide—zinc oxide) placed in the heating furnace (electric furnace) 74. In so doing, the temperature is controlled so that the cracker gas Gr containing terephthalic acid is heated at a temperature around 400˜600° C. By this means, terephthalic acid makes contact with the catalyst 75 at high temperature and is supplied to the condenser 62 in the next process. Once it is cooled by the condenser 62, a cracking product is obtained which contains mainly benzene, benzoic acid, and carbon dioxide, the carbon dioxide being the result of cracking of the carboxyl group of terephthalic acid.
In this way, when thermally cracking a PET molded form, although a large amount of terephthalic acid is generated, by passing it through the gas reforming unit 63, terephthalic acid which is a sublimation high boiling point compound is cracked in vapor phase, converted to a cracking product which does not crystallize (low boiling point compound).
On the other hand, when thermal cracking of the molten plastic Rd contained in the thermal cracking bath 2 is almost over, and if the residue plastic Rs remains, the linear driver 57 is controlled to open the open/close valve 51 in a state in which the agitate-scraping unit 12 is rotated, in which case, it is desirable that the residue plastic Rs have fluidity. By this means, the residue plastic Rs falls through the exhaust pipe 53 and is supplied to the interior of the bath main body 54 in the residue processing bath 52. The bath main body 54 is induction-heated by the high-frequency current fed to the coil 55. The high-frequency current is supplied from the high-frequency generation unit 81, and the bath main body 54 is heated to about 400° C., necessary for thermally cracking the residue plastic Rs. Therefore, the residue plastic Rs is further thermally cracked, and the cracker gas Gr generated in the process is supplied to the entrance port of the three-way valve 61 via the air line Pq, oil conversion processing being performed by the oil conversion processor 7. Also, when thermal cracking of the residue plastic Rs comes into the final stage, if only a sediment remains, the heating temperature of the bath main body 54 is increased to 500° C. to burn it off (Step S10). The bath main body 54 is heated to about 200° C. during standby. By installing a residue processing bath 52, thermal cracking, sediment burn-off, etc. can be performed efficiently and effectively. Moreover, cleaning and maintenance can also be performed easily as well as minimizing the residue sediment.
On the other hand, in the off-gas processor 16, the off-gas generated in the process of sequentially processing the waste plastic Ro, namely the off-gas generated inside the heating cylinder 8c in the extruder 8, the reservoir unit 42 of the vinyl chloride processor 41, the residue processing bath 52, the thermal cracking bath 2, the oil storage tank 66, etc. is made harmless and released to the atmosphere. In this case, the off-gas Go generated inside the heating cylinder 8c in the extruder 8 is led from the venting section of the heating cylinder 8c and is supplied into water W contained in the water seal bath 92 via the check valve 91. Also, the off-gas Go generated in the reservoir unit 42 of the vinyl chloride processor 41 is supplied into water W contained in the water seal bath 92 via the air line Pe and the check valve 91 . . . . Furthermore, the off-gas Go generated inside the bath main body 54 in the residue processing bath 52, the off-gas Go generated inside the bath main body 4 of the thermal cracking bath 2, the off-gas Go which remains inside the oil storage tank 66, etc. are also supplied into water W contained in the water seal bath 92 via the check valve 91 . . . in the same way. By this a part of harmful ingredient of the off-gas Go is collected by water W.
On the other hand, the off-gas Go floated up in the water seal bath 92 is supplied to the burn processor 17. The off-gas Go supplied to the burn processor 17 is burned by the burner 97 and sucked by the exhaust fan 98, and passes through the heat exchanger 93. In so doing, in the heat exchanger 93, the cylinder unit 94 is induction-heated by a high-frequency current flowing in the coil 95, and it is burned again at a high temperature of 800° C. or higher, desirably 1000˜1300θC. The high-frequency current is supplied from the high-frequency generation unit 81, by which the off-gases Go . . . generated in processing the waste plastic Ro, the molten plastic Rd, the residue plastic Rs, etc., and especially harmful gases such as dioxin, are made harmless ones and released to the atmosphere. In this case, because the cylinder unit 94 has a heat exchanger 96 formed of a mesh material or porous material in order to have a large contact area inside the cylinder unit 94, heat exchange efficiency is enhanced.
Therefore, by such an oil reconversion device 1a of the first embodiment form, because it uses the extruder 8 having the heating cylinder 8c and the extruding screw 8s which melts and extrudes the waste plastic Ro, rapid melting and further homogeneous and high-quality melting of the waste plastic Ro can be realized. Because the molten plastic Ro is extruded by the extruding screw and supplied to the thermal cracking bath 2 by utilizing the extruder 8, the process of supplying the molten plastic Rd becomes simple, and can be supplied more securely, as well providing ease of cleaning and maintenance.
The construction of an oil reconversion device 1b for waste plastics of the second embodiment form of the present invention is explained hereafter, with reference to FIGS. 9˜11.
Shown in
The thermal cracking bath 2 is constructed as shown in
Furthermore, a gas exit port 38 for a cracker gas Gr is installed on a ceiling 4u of the bath main body, and connects to the receiving side of the oil conversion processor 7, described later, via an air line Pp. Furthermore, installed on the ceiling 4u is a catalyst injector, not shown, which feeds a catalyst such as zeolite which promotes thermal cracking into the bath main body 4. Such a thermal cracking bath 2 is supported at a specified height by a machine stage 105 as shown in
On the other hand, the waste plastic injector 9 constitutes a feeder 6 which feeds the waste plastic Ro injected into an injection port 5 to the thermal cracking bath 2 via a direct feeding means Ub which has no melting bath. As shown in
Furthermore, an open/close damper 117 is installed in the injection pipe 112 located in the bath main body 4 side relative to the open/close valve 115, and can be rotated by an operating handle 118. In
On the other hand, no. 29 is a waste plastic pre-processor for obtaining the waste plastic Ro to be injected into the hopper 111. The waste plastic pre-processor 29 includes a separation process to separate waste materials, a crushing process to crush the waste plastic Ro, a washing process to wash the crushed waste plastic Ro, a drying process to dry it, etc. No. 7 is the same oil conversion processor as in the first embodiment form, which cools the cracker gas Gr supplied from the thermal cracking bath 2 via the air line Pp and converts it into oil. No. 63 is a gas reforming unit built in the oil conversion processor 7, which is the same as in the first embodiment form explained based on
The overall operation of the oil reconversion device 1b of the second embodiment form is explained hereafter, with reference to FIGS. 9˜12.
First, the waste plastic Ro is contained in the thermal cracking bath 2 using the waste plastic injector 9. The method of containing the waste plastic Ro is explained according to a flow chart shown in
Then, the dried waste plastic Ro is injected into the hopper 111, releasing the locking mechanism 121, and the open/close cap 114 is displaced up to the open position Zo indicated by the solid line in
In this state, the waste plastic Ro obtained by the waste plastic pre-processor 29 is injected into the hopper 111 (Step S25). Once a specified amount of waste plastic Ro is injected into the hopper 111, the open/close cap 114 is closed, and the open/close cap 114 is locked in the close position Zc by the locking mechanism 121 (Step S26). Next, the nitrogen gas feeder 82 is controlled to charge nitrogen gas Gi into the hopper 111 via the air line 120 and the air feeding port 119 (Step S27). By this means, the cracker gas Gr, etc remaining inside the thermal cracking gas 2 is prevented from directly contacting the air.
Next, the operating handle 118 is manually rotated to displace the open/close damper 117 to the open position Zo shown by the solid line in
On the other hand, the thermal cracking bath 2 has its bath main body 4 induction-heated with a high-frequency current flowing in coils 3 . . . . The high-frequency current is fed from the high-frequency generation unit 81. In so doing, the bath main body 4 is heated to about 450° C. which is necessary for thermally cracking the waste plastic Ro. The bath main body 4 is heated to about 200° C. during standby. The heating temperature of the bath main body 4 can be arbitrarily set according to the kind of the waste plastic Ro to be processed. Therefore, in the thermal cracking bath 2, the contained waste plastic Ro is melted and thermally cracked by a set high temperature of about 450° C. Namely, the waste plastic Ro become molten waste plastic by melting, thereby performing further thermal cracking of the molten waste plastic. Therefore, the thermal cracking bath 2 functions also as a melting bath to melt the waste plastic Ro. Also, agitation, etc. by the agitating mechanism unit 11 is performed in the same way as in the first embodiment form.
On the other hand, by the molten plastic being thermally cracked in the thermal cracking bath 2, the cracker Gr is generated and supplied to the receiving side of the oil conversion processor 7 via the air line Pp from the gas exit port 38. Afterwards, processings by the oil conversion processor 7, the off-gas processor 16, the burn processor 17, etc. are performed in the same way as in the first embodiment form.
By such an oil reconversion device 1b of the second embodiment form, because it is equipped with the thermal cracking bath 2 which functions also as a melting bath to generate the cracker gas Gr by melting and thermally cracking the waste plastic Ro, installability and general usability can be enhanced by miniaturizing the overall device, and reduction of unnecessary power consumption can contribute to reducing running costs. Because it is equipped with the waste plastic injector 9 which can directly inject waste plastic Ro into the thermal cracking bath 2, the process can be simplified, the waste plastic Ro can be smoothly and securely contained in the thermal cracking bath 2, and furthermore washing, maintenance, etc. can also be easily performed. In addition, because the waste plastic injector 9 has the open/close damper 117 installed to the injection pipe 112 in the bath main body 4 side of the open/close valve 115, the waste plastic Ro can be injected more stably and safely.
While the first embodiment form and the second embodiment form are explained in detail above, the present invention is not limited to these embodiment forms but can be arbitrarily modified, added to, or omitted from within parameters which does not deviate from the spirit of the present invention in the respects of detailed construction, shape, raw material, quantity, method, etc.
As described above, the oil reconversion devices 1a and 1b of the present invention can be preferably used in reconverting various kinds of waste plastics (polymer wastes) into heavy oil (grade-A heavy oil equivalent), etc.
Number | Date | Country | Kind |
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2004-8066 | Jan 2004 | JP | national |
2004-8067 | Jan 2004 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP05/00618 | 1/12/2005 | WO | 7/14/2006 |